CA2505819A1 - Indolyl pyrazinone derivatives useful for treating hyper-proliferative disorders and diseases associated with angiogenesis - Google Patents

Abstract

This invention relates to a compound of Formula I (I)and its use in treating hyper-proliferative disorders and diseases associated with angiogenesis.</SD OAB>

Description

Indolyl Pyrazinone Derivatives Useful for Treatina Hyper-Proliferative Disorders and Diseases Associated with Anaio enesis This application claims priority to US Provisional Application No. 60/425490, filed November 12, 2002, and to US Provisional Application No. 60/460,915, filed April 7, 2003, and to US Provisional Application No. 60/434,202 filed June 30, 2003.
Field of the Invention This invention relates to novel indolyl pyrazinone compounds, pharmaceutical compositions containing such compounds and the use of those compounds and compositions for the prevention and/or treatment of hyper-proliferative disorders and diseases associated with angiogenesis.
Description of the Invention Compounds of the present invention One embodiment of this invention is a compound of Formula I

R

R1 ~ ~ ~~Rs Ar ~ N~ Hs ~R12 H
wherein Ar represents a 6 membered aromatic ring containing 0, 1 or 2 N atoms;
--,-N X
R1 and R2 are each independently selected from H, halo, CF3, C(O)R9, (C1-C6)alkyl optionally substituted with up to two substituents selected from OH, (C1-C3)alkoxy, F, and phenyl, (C1-C6)alkoxy optionally substituted with one or two substituents each n -~-N X
independently selected from ' V and N[(C1-C3)alkyl]2 where each alkyl is independently optionally substituted up to two times with (C1-C3)alkoxy, NH(C1-C3)alkyl where said alkyl is optionally substituted with up to two substitutents each selected independently from OH, F, (C1-C3)alkoxy, J--N X
N[(C1-C3)alkyl]2, NH(C1-C3)alkyl, phenyl, pyrrolidinyl, and ' ~--i , N[(C1-C3)alkyl]2 where each alkyl is independently optionally substituted with up to two substitutents each selected independently from OH, F, phenyl, and (C~-C3)alkoxy, said alkoxy being optionally n --;-N X
substituted with ' ~ , pyrrolidinyl optionally substituted up to two times with N[(C~-C3)alkyl]2, phenyl optionally substituted with up to two substitutents each selected independently from (C~-C3)alkyl, (C~-C3)alkoxy, halo, CF3, and CN, Ar with the proviso that when contains 1 or 2 N atoms, R' and R~ must each be H, and, R' and RZ together with the adjacent C atoms to which they are attached form a ring selected from benzo, dioxolo and imidazo, said imidazo being optionally substituted up to two times with (C~-C3)alkyl, with the proviso that R' and R~ together with the adjacent C atoms to Ar which they are attached form a ring only when contains no N atoms;
R3 is selected from H, (C~-C4)alkyl, OH, N02, NH2, NH(C~-Cø)alkyl, NHC(O)(C~-C4)alkyl and NHC(O)phenyl, said phenyl being optionally substituted with up to two substituents independently selected from (C~-C3)alkyl, (C~-C3)alkoxy, halo, CF3, and CN;
R4 is selected from H, OH, halo, CN, C(O)R6, S(O)2R', OSi[(C~-C4)alkyl]3, tetrazolyl, thienyl, pyrrolyl, pyrimidinyl, oxazolyl, furanyl, (C~-C6)alkyl, (C~-C6)alkenyl or (C2-C6)alkynyl, each optionally substituted with OH, F, OC(O)NHphenyl, NHC(O)(C~-C3)alkyl, C(O)NH2, n --~-N X
C(O)NH(C~-C3)alkyl, C(O)N[(C~-C3)alkyl]2, ' ~ , (C~-C3)alkoxy optionally substituted up to two times with (C~-C3)alkoxy, NHC(O)NH(C~-C3)alkyl .where said alkyl is optionally substituted , with up to two substituents independently selected from OH, (C~-C3)alkoxy, F and phenyl, NHC(O)NHphenyl where said phenyl is optionally substituted with up to two substituents independently selected from (C~-C3)alkyl, n -'-N X
(C~-C3)alkoxy, halo, CF3, CN, and ' a NHC(O)N[(C~-C3)alkyl]2 where each alkyl is independently optionally substituted up to two times with (C~-C3)alkoxy, NH-phenyl, said phenyl being optionally substituted with up to two substituents independently selected from (C~-C3)alkyl, n --;-N x (C~-C3)alkoxy, halo, CN, and ' V , N[(C~-C3)alkyl]2 where each alkyl is independently optionally substituted up to two times with (C~-C3)alkoxy, phenyl optionally substituted with up to two substituents independently selected from (C~-C3)alkyl, (C~-C3)alkoxy, halo, CN, CF3, and n -~-N X
~J
pyrrolidinyl optionally substituted up to two times with N[(C~-C3)alkyl]z, (C~-C6)alkoxy optionally substituted with up to iwo substituents independently -~-N X
selected from (C~-C3)alkoxy, pyrrolidinyl, ' ~--~ , and N[(C~-C3)alkyl]~ where each alkyl is independently optionally substituted with up to two substituents independently selected from OH, F, (C~-C3)alkoxy and phenyl, N[(C~-C4)alkyl]2 where each of said alkyl groups are independently optionally substituted with up to two substituents independently selected from OH, (C,-C3)alkyl, F, (C~-C3)alkoxy, and phenyl, oxadiazolyl optionally substituted up to two times with (C~-C3)alkyl, phenyl optionally substituted with up to two substituents independently selected C(O)- X -J- x from (C~-C3)alkoxy, CN, (C~-C3)alkyl, halo, ~/ , ' C(O)(C~-C3)alkyl optionally substituted with up to two substituents independently selected from (C~-C3)alkoxy, OH, (C~-C3)alkoxy, F, and phenyl, and C(O)N[(C~-C3)alkyl]2 where each of said alkyl groups are independently optionally substituted up to two times with (C~-C3)alkoxy, pyridyl optionally substituted with up to two substituents independently selected from (C~-C3)alkyl, C(O)N[(C~-C3)alkyl]~ where each of said alkyl groups are independently optionally substituted up to two times with (C~-C3)alkoxy, and O-pyridyl optionally substituted with up to two substituents independently selected from CF3, halo, and (C~-C3)alkyl;
R5 is selected from H, halo, CN, (C~-C6)alkoxy, and (C~-C6)alkyl;
R6 is selected from OH, NHR'°, O-(C3-C6)cycloakyl, (C~-C3)alkoxy, O-(C2-C6)alkenyl, O-(C3-C6)alkynyl, (C~-C6)alkyl optionally substituted with up to two substituents independently selected from OH, (C~-C3)alkoxy, F, and phenyl, N[(C,-C4)alkyl]2 where each of said alkyl groups are independently optionally substituted with up to two substituents independently selected from OH, CN, N[(C~-C~)alkyl]2, (C~-C3)alkoxy, S{O)2-phenyl, S(O)2(C~-C3)alkyl, phenyl, furyl, tetrahydrofuryl, (C3-C6)cycloalkyl, and pyridyl, N[(C~-C3)alkyl]R$ where [(C~-C3)alkyl] is optionally substituted up to two times with (C~-C3)alkoxy, N[(C3-C6)cycloalkyl](C~-C3)alkyl where said alkyl is substituted with up to two substituents independently selected from (C~-C3)alkoxy, OH, CN, N[(C~-C4)alkyl]2, S(O)2-phenyl, S(O)2(C~-C3)alkyl, phenyl, furyl, tetrahydrofuryl, (C5-C6)cycloalkyl, and pyridyl, pyrrolidinyl optionally substituted with up to two substituents independently selected from NHz, NH(C~-C3)alkyl, N[(C~-C~)alkyl]~, C(O)NH~, NHC(O)(C~-C3)alkyl, NHS(O)2(C~-C3)alkyl, pyridyl, N[(C~-C3)alkyl]C(O)NH(C~-C3)alkyl, N[(C~-C3)alkyl]C(O)(C~-C3)alkyl, and (C~-C3)alkyl optionally substituted With up to two substituents independently selected from N[(C~-C4)alkyl]2, (C~-C3)alkoxy, and pyrrolidinyl, morpholinyl optionally substituted up to two times with {C~-C3)alkyl, thiomorpholinyl optionally substituted up to two times with (C~-C3)alkyl, piperazinyl optionally substituted with up to two substituents independently selected from pyrazinyl, C(O)NH2, C(O)NH-phenyl, C(O)-furanyl, C(O)(C~-C3)alkyl, C(O)NH(C~-C3)alkyl, C(O)N[(C~-C3)alkyl]R8, n --~-N X
S(O)2(C~-C3)alkyl, S(O)2-phenyl, pyridyl optionally substituted with up to two substituents independently selected from (C~-C3)alkyl, CN and CF3, phenyl optionally substituted with up to two substituents independently selected from (C~-C3)alkyl, CN, halo, CF3, and (C~-C3)alkoxy, (C~-C3)alkyl optionally substituted with up to two substituents independently selected from OH, F, phenyl, (C~-C3)alkoxy, /~
() N[(C~-C3)alkyl]2, pyrrolinidyl, C(O)-pyrrolidinyl, C O - ~ , -~--N X
~ , and pyridyl optionally substituted up to two times with (C~-C3)alkoxy, and piperidinyl optionally substituted with up to two substituents independently selected from phenyl, pyridyl, pyrrolidinyl and oxo-dihydrobenzimidazolyl;
n -~-N X
R' is selected from NH2, pyrrolidinyl, ' ~--~ , NH(C~-C3)alkyl said alkyl being optionally substituted up to two times with (C1-C3)alkoxy, NH-phenyl said phenyl being optionally substituted with up to two substituents independently selected from (C~-C3)alkyl, CN, (C~-C4)alkoxy, halo and CF3, N[(C~-C3)alkyl]2 wherein each alkyl is independently optionally substituted up to two times with (C~-C4)alkoxy, and phenyl optionally substituted with up to two substituents independently selected from (C~-C3)alkyl, (C1-C3)alkoxy, halo, CF3 and CN;
R$ is selected from (C~-C3)alkoxy, pyridyl, piperidinyl, pyranyl and phenyl, where each ring moiety is optionally substituted with up to two substituents independently selected from (C~-C3)alkoxy, and (C~-C3)alkyl;
n ~N X
R9 is selected from (C~-C3)alkyl, (C~-C3)alkoxy, OH, ' a , phenyl optionally substituted with (C~-C3)alkyl, (C~-C3)alkoxy, halo, CF3, and CN, N[(C~-C~)alkyl]2 where each of said alkyl groups are independently optionally substituted with OH, CN, N[(C~-C4)alkyl]~, (C~-C4)alkoxy, S(O)2-phenyl, S(O)2(C~-C3)alkyl, phenyl, furyl, tetrahydrofuryl, (C3-C6)cycloalkyl, and pyridyl, and pyrrolidinyl optionally substituted with N[(C~-C3)alkyl]2, Ar and, only when contains no N atoms, R9 is also selected from pyridyl, thienyl, and NHR'°;
R'° is selected from H, indolyl, (C~-C~)alkyl optionally substituted with up to two substituents independently selected from OH, F, phenyl, (C~-C4)alkoxy, NHC(O)(C~-C3)alkyl, -!-N X
S-(C~-C3)alkyl, benzimidazolyl, indolyl, thienyl, pyrazolyl, ' a , N[(C~-C4)alkyl]2 where each alkyl is independently optionally substituted with up to two substituents independently selected from OH, (C~-C3)alkoxy, F, and phenyl, phenyl optionally substituted with up to two substituents independently selected from (C~-C3)alkyl, (C~-C3)alkoxy, CN, halo, CF3, S(O)2(C~-C3)alkyl, S(O)2phenyl, and S(O)2NH2, pyridyl optionally substituted up to two times with CF3, imidazolyl optionally substituted up to two times with (C~-C3)alkyl, furyl optionally substituted up to two times with (C~-C4)alkyl, and pyrrolidinyl optionally substituted with up to two substituents independently selected from (C~-C4)alkoxy, (O), and (C~-C4)alkyl optionally substituted with up to two substituents independently selected from OH, (C~-C3)alkoxy, F, and phenyl, S(O)2-phenyl optionally substituted with up to two substituents independently selected from (C~-C4)alkoxy, (C~-C3)alkyl, halo, and CN, pyrazolyl optionally substituted with up to two substituents independently selected from (C~-C4)alkyl, (C3-C6)cycloalkyl, and phenyl, said phenyl being optionally substituted with up to two substituents independently selected from (C~-C4)alkoxy, (C~-C4)alkyl, halo, CF3, and CN, benzothiazolyl optionally substituted up to two times with (C~-C4)alkyl, thiazolyl, optionally substituted up to two times with (C~-C4)alkyl, thiadiazolyl, optionally substituted with up to two substituents independently selected from CF3, (C3-C6)cycloalkyl, and (C~-C6)alkyl, phenyl optionally substituted with up to two substituents independently selected --~-N X
from CN, halo, CF3, N[(C~-C4)alkyl]2, indolyl, ' V , O-pyridyl optionally substituted with C(O)NH(C~-C4)alkyl, (C~-C~)alkyl optionally substituted with up to two substituents n -~N x independently selected from pyridyl, ' '--~ , OH, (C~-C3)alkoxy, F, and phenyl, and (C~-C4)alkoxy optionally substituted with N[(C~-C4)alkyl]2 where one alkyl group is optionally substituted with phenyl, or n --;-N X
(C~-C4)alkoxy optionally substituted with pyridyl optionally substituted with phenoxy where said phenoxy is optionally substituted with up to two substituents independently selected from (C~-C4)alkyl and (C~-C4)alkoxy, and indazolyl optionally substituted up to two times with (C~-Cø)alkyl;
R" and R'2 are each selected independently from H, F and CI with the proviso that when ane of R~' and R'2 is F or Cl, the other must be H;
X is selected from O, S, CH2, and NH, and when X is NH, the H on NH is optionally replaced with pyridyl, pyrazinyl, phenyl, or (C~-C4)alkyl optionally substituted with up to two substituents independently selected from OH, (C~-C3)alkoxy, N[(C~-C3)alkyl]a, C(O)-pyrrolidinyl, N[(C~-C4)alkyl]2, and phenyl said phenyl being optionally substituted with up to two substituents independently selected from CN and (C~-C3)alkoxy, -'-N X
and when X is O, S, or CHI, the ' a moiety is optionally substituted -'-N X
by replacing any H atom in the ' U moiety with (C~-C4)alkyl;
or a pharmaceutically acceptable salt or ester thereof.
The terms identified above have the following meaning throughout:
Ar The term represents a 6 membered aromatic ring containing 0, 1 or 2 N
atoms. That is, one embodiment of Ar is an aromatic ring containing 6 C atoms.
Those 6 C atoms include the 2 C atoms that the Ar ring shares with the adjacent pyrazinone ring.
This definition also includes the aromatic ring described above where 1 or 2 C
atoms have been replaced with N atoms. The N atoms) may be located at any position on the aromatic ring except they may not be located at the adjacent C atoms that are shared by the Ar ring and the adjacent pyrazinone ring. . Examples of 6 membered aromatic N
containing rings include pyrido, pyrimido, pyrazino, and pyridazo.
R' and R2 are each independently attached to the Ar ring at any available C
atom except that when R' and R2 together form a ring, each of R' and R2 are attached to adjacent C atoms that are shared with the Ar ring so that the R'/R2 ring is fused to the Ar ring through 2 adjacent C atoms that are shared between the R~lR2 ring and the Ar ring.
R4 is attached to the indolyl moiety of the core molecule at either the 5 or 6 atom of the indole moiety.
R5 is attached to the core molecule at the 5 or 6 atom on the indole moiety that is not occupied by the R4 group. That is, when R4 is attached to the 5 atom of the indoyl moiety, then R5 is attached to the 6 atom of the indolyl moiety, and visa versa.

The term "optionally substituted" means that, unless indicated otherwise, the moiety so modified may have from one to up to at least two of the substituents indicated.
Each substituent may replace any H atom on the moiety so modified as long as the replacement is chemically possible and chemically stable. For example, a chemically unstable compound would be one where each of two substituents are bonded to a single C atom through each substituent's heteroatom. Another example of a chemically unstable compound would be one where an alkoxy group is bonded to the unsaturated carbon of an alkene to form an enol ether. When there are two substituents on any moiety, each substituent is chosen independently of the other substituent and so that, accordingly, the substituents can be the same or different.
The terms "(C~-C3)alkyl" and "(C~-C4)alkyl" and "(C~-C6)alkyl" mean linear or branched saturated carbon groups having from about 1 to about 3, about 4, or about 6 C
atoms, respectively. Such groups include but are not limited to methyl, ethyl, n-propyl, isopropyl, and the like.
The term "(C3-C6)cycloalkyl" means a saturated monocyclic alkyl group of from to about 6 carbon atoms and includes such groups as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl.
The term "(C~-C6)alkenyl" means a linear or branched carbon group having from about 2 to about 6 C atoms wherein at least two adjacent C atoms in the alkenyl group are joined by a double bond, with the proviso that when a C atom is double bonded to one adjacent C atom, it must be single bonded to any other adjacent C atom.
The alkenyl group is attached to the rest of the molecule through a single bond.
The term (C2-C6)alkynyl means means a linear or branched carbon group having from about 2 to about 6 C atoms wherein at least two adjacent C atoms in the alkynyl group are joined by a triple bond, with the proviso that when a C atom is triple bonded to one adjacent C atom, it must be single bonded to any other adjacent C atom.
The alkynyf group is attached to the rest of the molecule through a single bond.
The terms "(C~-C3)alkoxy", "(C~-C4)alkoxy" and "(C~-C6)alkoxy" mean a linear or branched saturated carbon group having from about 1 to about 3, about 4, or about 6 C
atoms, respectively, said carbon group being attached to an O atom. The O atom is the point of attachment of the alkoxy substituent to the rest of the molecule.
Such groups include but are not limited to methoxy, ethoxy, n-propoxy, isopropoxy, and the like.
The term "halo" means an atom selected from Cf, Br, F and 1.
The term "phenoxy" means a phenyl ring attached to an O atom, the O atom being attached to the rest of the molecule.

When "(O)" is used in a chemical formula, it means =O. That is, =O means an O
atom that is double bonded to the C or S atom to which it is attached.
The formula "N[C~-C3)alkyl]~" means that each of the 2 possible alkyl groups attached to the N atom are selected independently from the other so that they may be the same or they may be different.
When a phenyl ring or a heterocycle is attached to the rest of the molecule, it is attached by replacing any H atom on the phenyl ring or on the heterocycle, respectively, with a bond to the rest of the molecule, as long as the replacement is chemically possible and chemically stable.
n -~N X
means morpholinyl, thiomorpholinyl, piperidinyl or piperazinyl. Each is optionally substituted as described above.
Representative compounds of the invention are shown by way of example in Table I.
Table 1 Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]+ (Ex. No.) \ l N~ H~ 2.96 262.2 1 a N O
H

Nw H ~ 2. 86 307.2 1, 2 a N O
H
g HEN -Nw H~ 2.33 277.3 1, 2, 3 a N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]+ (Ex. No.) CI ' ~ N~ H' 3.66 330.2 1, 2 CI N O
H

O ~ N~ H' 2.85 372.3 1, 2 H3c. ~
O N O
H

H.
N\ ~ N \ j 2.71 292.3 1 N O
H

O 'w Nw I N~ 3.05 306.3 1 H
O ~ N O
H

02N ~
N\ ~ N~ 2.64 337.2 1, 2 H
N O
H

O ~ N~ H' 1.02 337.3 1, 2, 3 H3C.
O N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]+ (Ex. No.) HEN \ /
N\ ~ N~ 2.11 307.2 3 H
/ N O
H

pH3 ~ N\ ~ N\ / 2.70 352.2 1 H.
H3C.
O N O
H

pH3 ~ N\ ~ N \ / 2.68 347.2 12 H( H3C. I /
O N O
H

H3C~ ~ ~ ~
H C N I w N~. N~ 2.06 374.4 13 N O
H

N\ ~ N ' / 2.77 287.3 12 H.
N O
H
F
~H3 ~ N\ ~ N \ ' 2.84 340.2 1 H.
H3C. I /
O N O
H

WO 2004/043950 PCT/US2003/036003..
." , Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) (M+H]* (Ex. No.) N~ ~ N~ 2.92 280.2 1 H
N O
H

OH
2.56 306.3 22 ~ Nw N~
H
N O
H

N~ ~ N ~ N ~ 2.45 405.3 18 H ~O
N O
H

O~N -N~ ~ N ~ 2.81 332.2 12, 2 H
N O
H

H2N ~ /
N~ ~ N~ 2.88 302.3 12, 2, 3 H
N O
H

WO 2004/043950 PCT/US2003/036003 .
Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+fi~+ (Ex. No.) N
/ N 2.30 432.3 21 W. N\ H ~
O
N O
H

OH

/ 2.58 351.3 22 ~ N~ H~
N O
H

OH
HZN -/ 2.65 320.3 22, 3 H
I \ N\ N/
N O
H

OH
CH3 ~ ~ / 2.76 366.3 22 O ~ N~ N~
H3C.. I / H
O N O
H

02N .-OH3 ~ N\ ~ N 2.54 392.0 12, 2 H3C. I / H.
O N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]+ (Ex. No.) N
CH3 ~ \ / 2.48 492.2 21 O ~ N~ H~ N
H3c_ , O H O O..J

HEN -CH3 \
O ~ N~ ~ NY 2.31 362.2 12, 2, 3 H
HOC. I /
O N O
H
2g CN
N\ ~ N \ / 3.45 337.3 12 HI
N O
H
29 CHs O
N
CH3 I \ / 2.38 450.2 21 O ~ N\ N N
H3C ~ / H HsC CH3 O N O
H
3p CN

N\ ~ N \ / 2.96 382.3 12, 2 H.
N O
H

Ex. LCMS LCMS Preparative No. Structure RT ion Methods) (min) [M+H]~' (Ex. No.) OH
OZN -2.69 401.2 22 I \ \ N~
N O
H

O
CHs 2.70 321.3 1 I \ N\ H
a N O
H

CH3 2.67 340.3 1 F I \ Nw H
N O
H

N 2.44 404.3 18 \ Nw H
N
N O H
H

OH

2.88 370.3 12, 22,2, 3 I \ \ N~
/ /
N O
H

WO 2004/043950 PCT/US2003/036003, Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]+ (Ex. No.) 02N -' OH3 ~ N~ ~ N 2.68 385.1 1, 2 H3C. ~ / H.
O N O
H

N~ ~ N ~ 2.61 325. 0 2 H
N O
H

OH
O~N -' CH3 ~ ~ / 2.25 411.1 22 O ~ N~ N~
H3C. I / H
O N O
H

HEN -O ~ N~ ~ N~ 2.02 355.2 1, 2, 3 H3C. I / H
O N O
H

N~ ~ N Y 2.22 295.2 1, 2, 3 H
N O
H

WO 2004/043950 -- --PCT/US2003/036003' Ex. LCMS LCMS Preparative No. Structure RT ion Methods) (min) [M+H]* (Ex. No.) OH

CH3 I ~ l 1.94 381.2 22, 2, 3 O \. N\ N~
H
H3C. I /
O N O
H

H3C ~ N~ ~ N~ 2.93 315.3 12 H
HsC / H O

O~N -H3C ~ N~ ~ N~ 2.89 360.3 12, 2 H
HsC / H O

CN
Nw H~ 2.79 287.3 12 N O
H
CH3 I ~ ~ CN
O ~ N~ H' 2.68 347.2 12 H3C. I /
O N O
H

H3C ~ N\ ~ N~ 2.98 330.3 12, 2, 3 H
HsC / H O

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]+ (Ex. No.) 47 ~ CN
HEN '-\ /
N~ ~ N~ 3.27 351.4 12, 2, 3 H
N O
H

N \ /
N\ ~ N~ 2.26 405.2 49 H
O ~ N O
H
49 ~O~ CN
N Jl N\ ~ N~ 2.11 430.2 49 H
O / N O
H

O ~ N~ N~
H 2.21 430.3 50 N O
N H
C~
O

F I y Nw H~ 3.13 298.3 1 F N O
H
52 O~N -F I ~ N~ H~ 2.83 343.1 1, 2 F N O
H

Ex. i_CMS LCMS Preparative No. Structure RT fon Methods) (min) jM+H]~ (Ex. No.) 53 CO ~ F
N \
N\ ~ NY 2.33 423.3 49 H
O ~ N O
H

OH
O~N -/ 2.71 379.2 22 H3C I \ N\ N~
H
HsC / H O

OH

/ 2.79 348.4 22, 2, 3 H3C I ~ N\ N~
H
HsC / H O
56 ~ -CH3 O
N

/ 2.11 392.2 56 N~ H~
a N O
H
57 ~ H3 Hs N
N
HEN - CH3 1.73 433.1 56 \ /
I ~. N\ H ~
a N O
H

Ex. LCMS LCMS Preparative No. Structure RT lon Methods) (min) [M+H]'" (Ex. No.) N
O
N
H
H2N ~ 1,67 433.1 56 W Nw H
a N O
H

N
H N
H2N I ~ /
1.70 447.2 56 Nw N~ O
H
N O
H
60 ~ -CH3 O
N
H

/ 2.03 378.2 56 w Nw H~
a N O
H
61 / \
-N
O
N
HZN - CH3 1.71 439.1 56 /
N~ H~
a N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]* (Ex. No.) H
HZN -\ N\ ~ ~ ~ O ;g' ~ 2.24 503.2 56 NHa N O
H

N~., ,CH3 N
H2N ~ ~ ~ CH3 1.23 417.1 56 \ N~ H~
a N O
H

N O
HEN -2.03 390.3 56 N~ H~
N O
H

CHs 1.74 419.1 56 \ Nw N
H
N O
H

N~ N-CH3 HzN
1.22 403.0 56 I \ Nw N~
H
N O
H

WO 2004/043950 .....PCT/US2003/036003 Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+Hl'~(Ex. No.) 67 O '--~

NON

HEN
~

H3C 1.58 488.2 56 >

N~ H ~ H3C

a N O

H

6$ O

N~ N

H2N ~ N
/ 1.50 502.1 56 'w. Nw N
' H

N O

H

N~
N

/
~
N

HZN -2.17 466.9 56 w. Nw H~

I
a N O

H

~N
O

H2N - ~N
/ 1.62 516.0 56 N~ N O

H

N O

H

N

HZN -1.78 466.0 56 ~ N~ H~

N O

H

WO 2004/043950 _...PCT/US2003/036003 Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) (M+H~~'(Ex. No.) N N ~ ~N

HZN -1.73 466.3 56 w N~ H
a ~

N O

H

j--~

U

HZN _ N
1.58 500.2 56 W Nw ~

a H

N O

H

74 O ~ O

N N

O
HzN - j 258.2 2.16 (major 56 ~ N~ H/ ion) I

N O

H

N

HEN

f ~ 1.68 414.1 56 N\ / H

H

N O

H

N N~

-OH
H

HO 1.54 451.2 56 ~ N~ ~

a H

N O

H

Ex. LCMS LCMS Preparative No. Structure RT lon Methods) (min) [M+H]~' (Ex. No.) N NH
H !
HZN H3C~0 1.87 405.1 56 W Nw H~
N O
H

N
HZN -O 2.28 418.1 56 I ~ N~ H~ H3C
a N O
H

N
HEN
N~ ~ N \ / ~ NH 2.65 463.2 56 Hr N O
H

N

1.31 460.2 56 I ~ N~ H~ N
O N-' 81 O N~N
HEN ~/-1.57 457.2 56 I '. N\
a N O
H

WO 2004/043950 .. ._. PCT/US2003/036003 Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) (M+H]* (Ex. No.) H
HaN -1.66 425.1 56 \ Nw H~
a N O
H

H ~ ~N
HEN
1.66 425.2 56 N~ H~
a N O
H

_ H

1.63 425.0 56 \ Nw H~
N O
H

N

1.71 445.2 56 I \. N\ H~
N O
H

H
HZN
1.75 431.1 56 \ Nw H~
N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]+ (Ex. No.) 87 O eCH3 H
HEN
1.68 431.1 56 N~ H~
N O
H

N
_ H N
HzN ~ ~ H3C~ ~CH3 1.58 405.1 56 ~ ~ Nw N
H
N O
H

N
_ H S
H2N CHs 2.30 408.1 56 N\ H~
N O
H

H

1.65 417.1 56 Nw H~
a N O
H

N
H
HEN / '~~-O 1.99 445.2 56 H
N\ N/
N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]+ (Ex. No.) N
H

N 1.64 428.1 56 \ N~ N~
H
N O
H

O
N
_ H
HZN ~ ~ 2.92 396.1 56 N\ H
a N O
H

~N
N-' O
N 2.30 494.1 56 H

\ N~ H~
a N O
H
95 ' ~ H3 ~ Hs N
O
N 2.38 467.1 56 H
HEN -\ Nw N~
H
N O
H

Ex. LCMS LCMS Preparative No. Structure RT lon Methods) (min) [M+H]+ (Ex. No.) ~~NH
I \

N
H 2.71 435.1 56 N~ H~
a N O
H

N
HEN
1.67 431.1 56 I ~ N~ H~ N
N O
H

N

1.80 459.2 56 N~ H~ N

N O
H

N

~N 1.83 457.1 56 Nw H
N O
H

N

1.64 428.1 56 N\ N, _ H N~N,CH3 N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]+ (Ex. No.) N

\ / 2.29 388.2 56 I ~ N~ H~
a N O
H
102 ~ -CH3 ~- N

\ / 1.96 393.2 18 W Nw H~
N O
H

N
HZN
\ / 2.51 430.2 56 W Nw H~ S
N O
H
104 ~ -CH3 HsC O
~O N

/ 2.63 434.1 104 Nw H~
a N O
H

NON
HzN HsC_O
/ 1.45 447.0 56 W Nw H ~
a N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]+ (Ex. No.) NON
HEN O
1.64 500.1 56 ' ' CG
\ Nw NY
H
N O
H
107 O-CHs O
N
, HZN - CHs 2.47 440.1 56 I \ N~ H
a N O
H
108 / ' O
N
CHs HzN ~ / 2.48 410.1 56 I \ N\ H
a N O
H

N~N-CHs / ' O
N
H 2.41 450.1 56 HZN -/
\ Nw H~
a N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]+ (Ex. No.) N
HEN -2.11 374.3 56 \ N~ N~
H
N O
H

N
O
N 2.46 481.1 56 H

\ N\
N O
H

N
O
N 2.19 479.3 56 H

\ N\ N ' , H
N O
H

N
N
O
N
H
H2N - 2.03 413.9 56 \ Nw N~
H
N O
H

WO 2004/043950 PCT/US_200_ 3/036003 ll~;ai j.,~, ~"~" J ,.., ~~, jr rt;~ swJ ,.'~:~~ ,.~' ~~ "".'~t ~v..:..:f jl'".,'f~ ~G°...,iE ;'""ia Ex. LCMS LCMS Preparative No. Structure RT lon Methods) (min) [M+H~~ (Ex. No.) O \ /
/ ~N
O
N
H 2.86 489.3 56 /
N~ H~
a N O
H

° \ / ~cH3 v ~~
N
O
N
H
HzN - 3.01 519.2 56 \ /
W Nw H~
'/ N O
H

N
HzN ~ / / \
w Nw , N~ 1.73 508.1 56 ,.- H N
H O
N

N
HzN - / \
\ / 1.90 494.9 56 W Nw H ~
N
H O
O

Ex. LCMS LCMS Preparative No. Structure RT lon Methods) (min) [M+H]+(Ex. No.) / CN
~N

\

HEN -\ /
~
~

N~ 2.75 490.3 56 N

aH

N O

H

11g-NC

O

N ~ /
N

O
N

HEN -\ / 2.61 491.0 56 ~ N~ H ~

N O

H

O

~N ~ j CN

N

HEN -\ /
~

N~ 2.63 491.0 56 N~

aH

N O

H

O

N

\ l ~

HEN -\ / 1.37 495.1 56 w Nw a N O

H

Ex. LCMS LCMS Preparative No. Structure RT lon Methods) (min) (M+ti]+ (Ex. No.) N~ \ ~ o HzN - CH3 I ~ N~ ~ H~ 2.34 495.1 56 ~N O
H

O
V \/
HEN -\ / 2.63 490.1 56 I ~ Nw H~
a N O
H

O
~N \ /

\ / 2.71 483.1 56 ~ N~ H~
N O
H

NCH / N
H2N - s 1.93 467.0 12, 2, 22, 56 HsC I ~ Nw N~
H
HsC / H O

N
HZN '-' \ / ~N 2.07 485.2 12, 2, 22, 56 H3C I ~ N~ Hr' Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H)~ (Ex. No.) 127 0 ~ N-N~N \ /

\ /
H3C \ N~ ~ N~ 1.98 494.0 12, 2, 22, 56 H
HsC / H O
128 ~ Ha .
~ Hs N
O
N
H2N - CH3 2.12 469.1 12, 2, 22, 56 F I \ N~
F N O
H

N

t ~ / N 2.26 493.1 12, 2, 22, 56 F I \ Nw HY
F N O
H

NCH / N
H2N - s / 2.12 475.0 12, 2, 22, 56 F I \ N\
F N O
H
131 ~ -CH3 O
N

j 2.53 428.1 12, 2, 22, 56 F I \ N\
F N O
H

Ex. LCMS LCMS Preparative No. Structure RT lon Methods) (min) [M+H]'" (Ex. No.) 132 0 ~--~ N-N~N \ /
HzN -/ 2.16 502.0 12, 2, 22, 56 F I W Nw H
F N O
H

O
N

\ / 2.24 420.4 12, 2, 22, 56 H3C I ~ N\
H3C H O .

Hs Ha N
O
N
H2N - CH3 2.47 501.1 134 CI I ~ N~
CI N O
H

O \ /
N
N

/ 2.87 410.2 56 N\
N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]~ (Ex. No.) O
N
HEN \ ' 1.82 416.9 56 \ N\ I N ~--~
H
N O
H

N
O
N
HzN - 1.84 451.1 56 I
~ N~ H~
a N O
H

O O~CH
N' s HzN - ,CHs I ~ ~ 2.58 364.2 56 ~ N~ N~
H
N O
H

N
N,CH3 N I ~ ~ O~'OH3 2.09 445.0 56 N
H
N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) (M+H]+ (Ex. No.) N~ /
O
N
HzN - 2.09 465.2 56 \ /
w N\ Hi N O
H

NCH / N
HZN - a \ / 2.18 489.1 12, 2, 22, 56 \ N\ N~
H
N O
H
142 ~ -CH3 O
N

\ / 2.77 442.2 12, 2, 22, 56 N\ N, H
N O
H
143 O ~--~ N-N~ j \ l HZN -\ /
N~ ~ N~ 2.37 516.0 12, 2, 22, 56 H
N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]+ (Ex. No.) 144 Hs ~
CH~

~
N

O

N
, HZN - CHs 2.42 483.1 12, 2, 22, / ~ N~ N~
H

N O

H

N

HZN -t \ / N 2.65 525.1 12, 2, 22, CI

~
~

~

CI N O

H

O

N O

U

HZN -\ / 2.71 458.1 12, 2, 22, ~ N~
CI

I

CI N O

H

N

HZN -\ / N 2.31 507.3 12, 2, 22, ~
~

N O

H

148 O ~ N-N

~
\ /

\ /
~

Me0 ~ N~ 1.83 526.0 12, 2, 22, N~ 56 H

Me0 ~ N O

H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]+ (Ex. No.) 149 ~ -CH3 O

N
, HaN - CH3 I \ / 2.11 452.2 12, 2, 22, Me0 I ~ N\ N~
H

Me0 ~ N O

H

Ha ~ Hs N

O

N

HZN - CH3 1.64 493.1 12, 2, 22, I \ /

Me0 I ~ N\ N~
H

Me0 ~ N O

H

N

HEN - NH
\ /
~

I 1.97 431.0 151 H
C
p N~

N O

H

152 Me ~
O

N

/ \ CHI

152, 12, 2, 2.50 468.2 H N - 22, 56 I

N~
N

H

N O

H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]+(Ex. No.) N

-NH

i H C 2.29 495.2 151 \ / s '~s~0 ~

N
CH

N O

H

N

HzN - NH2 / 1.29 389.0 151, 3 Nw N~

H

N O

H

N \ /

HEN -2.87 464.2 155 ~ N~ H~

a N O

H

N O
U

HEN -\ / 1.51 375.8 156 N
~

I ~
~ H

N O

H

\ /

1.72 307.1 156 H.
N~ ~ N

N O

H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]+ (Ex. No.) 158 O ~--~ CH3 N~% _S~O

/ 2.09 467.1 158, 56 N~ H~
a N O
H

N

1.58 359.9 156 I \ N~ H/
a N O
H

HEN OMe N\ ~ N~ 2.14 365.1 160 H
N O
H

~j N
HzN -/ 1.63 451.9 156 N~ H~
a N O
H
162 ~ -CH3 O
N

H ~ ~ ~ 1.70 446.2 12, 2, 22, 56 N w Nw N~
H3C-y I / H
N N O
H

Ex. LCMS LCMS Preparative No. Structure RT lon Methods) (min) [M+H]+ (Ex. No.) ~
N
, / 1.70 377.9 156 w Nw H~

N O

H

H~c~
N

N

2.16 582.2 336, 2, 22, O

I

~ N\
i I
H

N O

H

N O CHa N
H

E

2.98 414.2 56 '\ N\
~

H
a N O
H

N
N ~-( I-H

E
~

2.12 418.0 56 N~ Hj N O

H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]~ (Ex. No.) 167 '-CH3 O

N
H
N \ /

E

I \ / 3.40 467 56 N~ Hi a N O

H

168 ~CH3 O

N
, I \ / 2.94 390 56 W Nw H~

a N O

H

N O
H
N \ I

z I \ / 2.96 414.2 56 ~
N

w H

a N O
H

O

N
-C

H2N 2.71 420 56 \\ //

I

W Nw N

H

N O

H

N~

N.CH3 _ ~N

N 1.02 402.9 156 I \ / CH3 w N
H

N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]+ (Ex. No.) N
-~
N 2.21 450.0 156 \
w H
a N O

H

n ~N-CH3 HZN -~
N 1.07 388.9 156 \
w H
a N O

H

174 _ N

U ~~
N

HEN -~
N 1.97 452.9 156 \
~ H
a N O

H

O

N O

V

\

152, 12, 2, HEN - 2.43 466.3 22, 56 \ N~ H~

a N O

H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]* (Ex. No.) 176 ~ / \

O ~--1 N~1 _S~O

HZN ~ / ~ 2.61 529.1 158, 56 I

Nw N
H

N O

H

/ \

H2N \ / 2.93 378.3 152 I

Nw N
H

N O

H

O ~ F
N
N ~ / F

~
N F

HZN -\ /

I ~ N~ I H~ 2.96 534.0 56 a N O

H

\ /

N\ I NY 2.23 291.2 12, 2, 3 H

N O

H

O f---~ ~--CH3 UN_S~O

HZN - O

I \ / 2.32 495.1 158, 56 ~ Nw H~

a N O

H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]+ (Ex. No.) 181 ~CH3 O
N
H2N '- ~-CN
I \ / 2.99 415 56 N~ H~
a N O
H

VN ~ /
HzN N

I \ / 1.84 480.0 56 'w N\ N ~
H
N O
H

F
O
_ a ~ I
N
HzN \ / 3.04 534.0 56 w Nw I N
H
N O
H

O
NON ~ /
HzN - N
I \ / 1.88 480.1 56 ~ N~ H~
a N O
H
185 O'O
O \ /
N
, HzN \ ~ 2.37 502.2 56 W Nw I N
H
N O
H

Ex. LCMS LCMS Preparative No. Structure RT lon Methods) (min) [M+Ha+ (Ex. No.) 186 ~ -CHI
O
N
HEN ~ / ~ -CH3 2.16 436.3 56 W Nw I N
H
N O
H

HZN -' / \
I \ j 2.14 467.2 156 I W Nw H~ - N
O '--O

N
NH
N N I \ / CH3 1.69 403.0 56 N O
H
189 OMe O
VN \ /
HaN OMe I \ / 2.71 525.1 56 ~ N~ H
a N O
H
190 ~-OMe O
HEN
I \ / 2.26 387.2 18, 2, 3 F I \ N\
F N O
H

Ex. LCMS LCMS Preparative No. Structure RT lon Methods) (min) [M+H]* (Ex. No.) 191 ~--OMe O
I \ / 2.30 372.2 18 F I \ N\ Hi F N O
H

OzN / \
I \ / 2.14 497.1 156 y N\ HY - N
H O ~O
19S OMe / \
HzN \ / 3.03 383.3 152, 1, 2, 3 Nw I N
H
N O
H
194 ~ -CH3 O
N
HaN - ~CH3 I \ / HsC 2.37 420.4 56 N~ H~
a N O
H
195 O ~---~ O
N N--~
HEN - V NH

N I \ / CH3 2.12 474.3 214, 3 N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H~+ (Ex. No,) O ~ S \ / OMe N
H

\ / 2.77 490.1 196 I \ Nw N~
H
N O
H

O \ /N
\ / CI 3.77 423.2 217 ~ Nw H~
a N O
H

H
N
HzN / ~N
\ / 2.45 397.2 56 Y
Nw . N
H
N O
H

N

y N' Hr' \ / 2.74 411.1 56 N O
H
200 ~ H3 O
N O
HEN -\\ /, CH3 2.81 418.2 56 W N~. I N
H
N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]'"(Ex. No.) 201 o OH

O~N -/ 2.42 386.9 12, 2, 22 F
N
~

I ~
~ H

F N O

H

\

/
CI ~ N~ ~ NY No dataNo 12 H data CI ~ N O

H

N -\ /

CI ~ N~ ~ N~ No dataNo 12, 2 H data CI ~ N O

H

OH

O~N -/ 2.68 No 12, 2, 3 r data N
CI

\ H
I ~

CI N O

H

\ /

N~ ~ N~ 2.28 337.0 156 aH

N O

H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]+ (Ex. No.) -OMe O
3.00 336 18 ~ N~ H~
a N O
H

OH
N~ ~ N \ , 2.27 278.2 217 H.
N O
H

CN
N ~ N\ ~ N~ 2.09 341.3 12 HaC--~~ I ~ H
N N O
H
209 ~-OMe O
HEN
2.41 351.2 18, 2, 3 I W Nw H~
a N O
H

N O
V
OaN
1.73 406.0 156 ~ N~ H~
a N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]+ (Ex. No.) / \

o2N ~ 2.96 408.1 152, 1, /
i ~

w Nw N

H

N O

H

N

NH
ON - , I \ / CH3 1.54 433.0 151 w Nw N, a N O

H

213 OMe \ / 3.34 368.2 152, 1 I
Y

\ N\
N

H

N O

H

HZN - N NH

I \ / CH3 I--CH3 2.17 488.1 214, 3 ~ N~
' CH3 I
H
a N O

H

215 O ~---~ O

N N--.' ~---~ CH3 H~N

I \ / 1.90 431.1 214, 3 ~
w Nw H

N O

H

Ex. LCMS LCMS Preparative No. Structure RT lon Methods) (min) [M+H]+ (Ex. No.) 216 O ~ O
N N
HzN - ~J ~--CHs 2.18 459.1 214, 3 I \ N\ Hi N O
H

w o \ ~N

CI 2,gg 438.2 217 L ~ N~ H~
N O
H

N~ OII
H2N N~NH
\ / CH3 CH3 2.05 460.1 214, 3 I ~ N\ N' H
N O
H
219 O ~ O
N N--HZN - ~---~ NH

1.98 446.0 214, 3 N~ N~
N O
H

w o \ ~N
HZN -\ / F 3.14 406.2 217 N\
a N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]+(Ex. No.) N N OMe ~/

_ ~ ~~
H2N \ f N~OMe ~ ~/
~

N~ 1.92 540.1 214, 3 N

aH

N O

H

w O \ ~N

HEN

\ / 3.21 438.2 217 ~ N~ N~
H

N O

H

223 OMe O

N

- CH

s HzN

\ f 2.19 406.0 56 \. N\
~

H
a N O

H

224 O ~ O

N N-- U NHa f 1.76 431.6 214, 3 N~ H~

a N O

H

225 O ~--~ O

N N-NH

HEN

~ 2.49 508.1 158, 56 \ f N\
N
\ f .

H

N O

H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) (M+H~+(Ex. No.) N N

~ \

N 1.86 480.1 214, 3 /
N

~
~ H

a N O

H

S-CH

~

~--~O

N

CH
H2N ~ 2.22 440 56 / .
~
>
~

---N\
N

H

N O

H

~-CH3 O-Si-CH3 \ / 3.98 392.3 228 ~ N~ H ~

N O

H

~-CH3 O-Si-CH3 - CH

HEN

\ / 3.38 407.3 228, 2, 3 ~ N~ H ~
a N O

H

230 OMe \ / OMe N~ ~ N ~ 2.70 322.3 1 aH

N O

H

Ex. LCMS LCMS Preparative No. Structure RT lon Methods) (min) [M+H]+ (Ex. No.) 231 OMe OMe N\ ~ N~ 2.67 340.3 12 H
N O
H

\ /
N\ ~ HY 1.97 288.3 12 N
N O
H

/ cN
Me0 I ~ N~ H' 2.64 No data 12, 2 Me0 N O
H

\ / F
I w N~ H ~ 2.91 280.2 1 N O
H
235 N~N''N
NH
OZN -/ 2.22 375.0 12, 2, 236 ~ Nw H~
a N O
H
236 N~N''N
NH
HZN
/ 2.09 345.0 12, 2, 236 I \' N\ H~
N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H~+ (Ex. No.) \ /
CH w Nw I NY 2.00 373.1 13 .N~ ~ / H
HsC H H O

/ o w N~. H~ ~N 2.00 405.2 18 ~J
N O
H
239 1-IzN
\ / cN
Me0 I ~ N~ H' 2.20 362.2 12, 2, 3 Me0 N O
H

/ o w N~ H~ ~N 2.12 403.2 18 N O
H

I \\ // o Me0 ~ N~ Hr ~N~
2.10 463.3 18 O- v 'N
Me O
H

\ /
~ N~ N~ 2.27 428.3 49 H
~N~O ~ H O
O

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]~ (Ex. No.) \ / OMe I w N~ H~ 2.84 292.3 1 N O
H

\ /
N~ ~ N~ 2.03 415.1 13, 49 H
~N~
N N O
H H

\ /
~N~N ~ N\ ~ N~ 1.89 415.1 13, 49 OJ I / H
N O
H

p ~. N~ H~ 2.07 390.2 13, 49 ~N.~. I
N N O
H H

\ / OMe I ~ Nw H~ 2.22 307.3 1, 2, 3 a N O
H

N
HEN - N~CH3 / HsC 1.20 417.1 56 N\ N~
H
N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+~N]+ (Ex. No.) \ l N~ H ' 2.94 349.2 13 MeO~, I i N N O

CH3 I \ /
Me0'~N I ~ N~ N~ 2.43 349.2 13 H
N O
H

\ /
N~ H' 2.88 374.2 13 MeO~
N N O

MeO~NH3 w N~ I N\ / 2.48 374.2 13 H
N O
H

\ /
F ~ N~ ~ N~ 2.82 323.1 12 ~~ H
F ~ N O
H

O~N
F ~ N~ ~ N \ / 3.07 368.1 12, 2 H.
F ~ N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H~+ (Ex. No.) 255 O cH3 N
H
O ~ ~N
/
O
N 2.82 546.0 56 H

\ N~ H~
N O
H

N
O ~--~ N
N
H
HEN - 2.12 428.1 56 /
\ N~ Hi a N O
H

O ~ ~ CF3 N N
H
HaN -/ 2.49 479.2 56 \ N~ H i a N O
H
258 OMe O
N
, / 2.24 2.24 12, 2, 22. 56 H3C I \ N\ Hi HsC H O

Ex. LCMS LCMS Preparative No, Structure RT Ion Methods) (min) [M+H]'" (Ex. No.) O \ /
MeO.~.~N ~ N~ ~ N~ 2.19 392.3 12, 2, 22, 56 N O
H

O \ /
H3 N,,,, N w N~. I H~ 1.16 417.1 12, 2, 22, 56 H3C ~ I ~ N O
H

o ~ \ /
Me0 I ~ N~ Hs 3.23 320.1 1 ~ N O
H

o ~ \ /
Me0 I ~ N~ H ~ 2.50 351.3 1, 2 N O
H
263 ~ OMe O
N

I \ / 2.32 422.4 56 W Nw H~
N O
H
264 ~ Me O
N

/ 2.71 460.1 56 N~ H~
N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]+ (Ex. No.) O
N
H
HEN
N\ ~ N \ / 2.69 472.4 336, 2, 22, 56 H
O
F

N~ H~ 2.94 278.7 266 a N O
H

O
--N
N H
H
HEN \ / 156, 214 I \ N\ H
a N O
H
268 ~ Me O~-N
H
HZN

W Nw H
N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) (M+H]'"(Ex. No.) 269 OMe O
O;S_N

-/

I \ N~ H~
a N O

H

N
Ov -~
S
N
~ ~OMe \ Nw H~

N O

H

N

HEN -\ / 152, 1, 2, \ N' I

N O

H

f \N

HzN ~ / 152, 1, 2, \ N\ H

I
a N O

H

Ex, LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]* (Ex. No.) 273 OMe 319, 2, 3 N~ H~
a N O
H

O
HEN 319, 2, 3 N\ N~
H
N O
H
275 ~ Me O
N
H
HEN
j 56 Nw N~
H
N N O
H

N\ Hue' 3 N~~
N O
H

N W Nw H~ 3 I
N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]+ (Ex. No.) N
, \ / 56.
N~ N~ N~
'H .
/ N O
H

N~ H ~ 336, 2, 3 N O
H

O I \ /
~N / I Nw N~ 1, 2, 22, 3 J H
O~ \ N . O
H

H2N \ /
~N~Nw N 1, 2, 3 'T~ H
N N O
H
282 O~N -\ /
~~Nw N~ 1, 2 H
N~ N O
H

w Nw N~ 1, 2, 3 H
N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) (M+H]k (Ex. No.) N'Nw Nw N~ 1 'H
N O
H

Nw H~ 1 N.N N O
H
286 O-CHs N\ N\ H 1 N.~/
N O
H

CHs ~ I ~ / pH
O w N~ H ~ 1, 2, 22, 3 H3C..
O N O
H

~N'~O, .~, N~ H HsC' CHs 56 a N O
H

1 ~ / N
w Nw N~ HsC ~~/ 56 H N
N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) (M+H]+ (Ex. No.) \ ~ NUJ
N~ H 56 N O
H

\ / NON

~. Nw NY N
H , O

NV N f ~ N~ HA 56 a N O
H

\ ~ H / N
Y
N~ N 56 H
N O
H

2 \ / N
w N~ ~ NY ~ 56 H N
H O

H2N I \ f N
Nw H~ 56 a N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) (M+H]* (Ex. No.) HEN O ~
/ ~N
Y
N,~ N CH3 56 H
N O
H
297 H N .' O
\ / N~ CN
~N ~ 56 ~ Nw H 1 N
N O
H
29$ H N - O
\ / N'~l ~' N~ N~ v N ~ ~ 56 H
N O N
H CN

HEN -I
Nw H~ H3C / N 56 F N O
H

HEN
/ N~O.GH3 F I ~ N~ N~ CH3 56 H
F ~ N O
H
30'I H N - O
\ / N~1 F ,~ N\ N~ ~N N\ 56 H
F ~ N O
H
302 H N -. O
\\ // N~O~CH~
H3C '~ N~ I N~ GH3 56 H
HsC ~ H O

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]'" (Ex. No.) \ / N
w N~ I H~ ~ 56 N'CH
H O HsC 3 304 N.N ~CH3 O
HEN -I \ / 2.32 359.3 304 \ Nw N~
H
N O
H

N~OH
HZN ~ ~OH
I \ / 1.89 394.2 56 1 W N, N, aH
N O
H

N

I \ / 1.94 364.2 56 \ Nw Hi a N O
H
307 ~ -CH3 O
N
HEN -~\ /~ 2.74 446.2 307 Nw I NT-' aH
N O
H

Ex.- LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]+ (Ex. No.) 308 ~ -OH3 O

N, N ~(\~~
H

Z 2.86 460.2 307 .

N~ N~

H

N O
H

~

N
H ~( N ~

~ \~/

/ 3.01 474.2 307 Nw N~

H

N O
H

O ~
' /
\ /
NH
N~N

HaN
~

/ \ 2.04 520.3 56 N~ ~

a H

N O
H

~

N

HzN

I\ / 1.02 475.3 56 N ' N

H

N O

H

312 ~ -CH3 O~N -/ 2.63 395.0 160 Nw N~
H

N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]+ (Ex. No.) 313 ~ -CH3 O

N

NON

/ ~ 2.30 462.2 307 N~ H~

N O

H

314 ~ -CH3 N
, \ / 2.42 410.1 56 Nw N~

H

N O

H

N~

_ 'r N.C

O
~ / CH3 ~
~

N~ 2.14 521.0 12, 2, 22, ~
~ H
I
~

/
N O
~

H

N N

U

HEN -O \ /
~

N~ 2.18 551.0 12, 2, 22, H
I ~

N O

H

N

O
/ 2.88 492.2 12, 2, 22, N~ N~

~
~ H
I

/
~ v -N O

H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+hl]* (Ex. No.) 318 H3~

~O
, / 1.93 349.45 319 Nw Hi a N O
H

N--, CHs \ / 1.86 377.47 319 H3C I \ N\ N~
H
HsG / H O

N
O

\ , 1.75 409.3 319 H C~O \ N~ H

H3C. I /
O N O
H
321 ~ -CH3 N

3.18 496.1 12, 2, 22, 56 / N~ N~
H
N O
O H

\ /
F3C .~ N~ ~ N~ 3.16 395.5 12 H
N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+hl]+ (Ex. No.) \ /
N~ I NY 3.16 395.5 12 H
FaC / H O

N
HEN -O
I \ / 2.71 478.2 12, 2, 22, 56 N~ H
~N O
H

N
HEN
I \ / 2.85 478.2 12, 2, 22, 56 N\ H/
_H O
O

N
HzN - /
I \
N~ Hr O CH3 2.39 568.0 12, 2, 22, 21 H O
N
~CH3 -O

N
H2N \ / / \
\ N~ I Hr"-' 2.95 553.3 12, 2, 22, 21 H O
N--~

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+Hj~ (Ex. No.) N
HEN - / \
\
N~ HY O CH3 3,01 587,3 12, 2, 22, 21 H O
/ \ N

N
HZN ~ / / \
N
O O-CH3 2.67 541.3 12, 2, 22, 21 / H O
N
C ~H3 CH3 ' OH
HZN -/ 2.23 339.1 12, 2, 22, 3 F ( \ Nw N~
H
/ N O
H

OZN
\ /
F3C ~ N~ ' N~ 3.01 400.0 12, 2 H
/ N O
H

OZN
\ /
N~ ~ N~ 3.01 400.0 12, 2 H
FsC / H O

Ex. LCMS LCMS Preparative No. Structure RT lon Methods) (min) [M+H~+ (Ex. No.) 333 Ha H3 ~
N
N
O 2.16 582.2 336, 2, 22, 56 \ N~ H/
\ ~ H O
F
334 ~ 0 OH
O~N
2.72 419.0 12, 2, 22 F3C I \ N\ N~
H
N O
H

OH
HzN -O
2.82 425.2 12, 2, 22, 3 \ \ Nw N
I~ /~ H
'N O
H

F
\ N~ ~ N 3.49 381.3 336 H
N O
H

\ N~ H~ 3.49 381.3 337 \ ~ H O
F

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]+ (Ex. No.) 338 o H
N
?-S
z H N I ~ / NJN J 2.88 404.2 12, 2, 22, 21 I \ N\ H~
a N O
H
339 ~ -CHs O
N
HaN CHs \ J 2.71 460.1 12, 2, 22, 56 F3C I \ N\ H
N O
H
340 o H
N
HaN - / \
\ / 2.21 487.3 56 y N' HY
H O N\ /

F OZN -\ J
N\ ~ N 3.16 426.0 336, 2 H
N O
H

/
N~ H~ 3.16 426.0 336, 2 I ~ ~ H o F

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]t (Ex. No.) N
S
H2N \\ // N J
3.06 403.1 12, 2, 22, 21 \ N\ N
H
N O
H

N CHs HzN - / N.
/ ' N 3.17 456.2 12, 2, 22, 21 N
I / w H HsC CHs N O CHa H

N
HEN
2.50 406.5 12, 2, 22, 56 \ N\ H
N O
H

O \
\ I \ N\ ~ N 3.32 393.2 336 H
N O
H

\ /
N
I \ ~ H 3.32 393.2 336 I .~ ~ H o Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]+ (Ex. No.) 348 ~ -CH3 O

O
.

.
_ N

, / 413.6 354 N~ H~
a N O

H

N

?'-S

z \ / NIN~
N

~ 2.63 474.0 12, 2, 22, N
\ ~ N

I
H

N O

H

350 o H

N

>-S
N
/

\ / ~
N

N I 'CH 2.88 490.0 12, 2, 22, ~

CH3 s N O

H

N
>"-S

O~N
/

\ / N
~ CH3 ~ N ~CH 3.02 504.1 12, 2, 22, ~

\
N

a H H3C

N O

H

N

?'-S
/
N

\ / N

N CF3 3.03 501.9 12, 2, 22, N\ H

a N O

H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) (M+H]+ (Ex. No.) 353 ~H
- N

OzN
O
~ ~

\ N\ ~ NY 3.48 478.1 375 aH

/ N O

H

~
.O
O

.
_N

, CHs HaN 2.59 428.5 354 /

\ Nw Hr N O

H

N
-~S

HzN

N 3.76 459.1 12, 2, 22, N
w CHs H H H

C
N O s H

N
- ~S

HzN

N / 3.41 467.0 12, 2, 22, r 21 \ N~ H \

I

O CHs N

~
S
// -HzN ~ ~ N
CHs 3.04 460.1 12, 2, 22, . 21 N ~ N I _CH

s CHs w H

/ N O

H

Ex. LCMS LCMS Preparative No. Structure RT fon Methods) (min) [M+hi]~' (Ex. No.) N~'°~ .CN3 N
H2N ~ ~ / ~H3 1.66 435.1 12, 2, 22, 56 F I \ N\
N O
H

N~, _ ~~ N,CH3 HzN ~ \ / CH3 1.66 435.1 12, 2, 22, 56 N~ H~
F N O
H

_ N~'°~ N.CH3 z N N ~ \ / CH3 2.14 521.0 12, 2, 22, 56 ~I I~
H O
O

OH
HZN -/ 2.23 339.1 12, 2, 22 I \ N~ Hr F N O
H
362 ~ -CH3 O
N

\ / 2.71 460.1 12, 2, 22, 56 I ~ N~ Ni H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]+ (Ex. No.) N

HEN -/ 2.50 406.5 12, 2, 22, i 56 N

\
~ H

F N O

H

364 O ~

_ N~/ ~O

HEN

CHs /
~
Y

F \ N~ 1.71 465.3 12, 2, 22, H

N O

H

NV ~O

HzN C

Hs I
~

\ N~ 1.71 465.3 12, 2, 22, H

F ~ N O

H

N

HZN -/ 2.38 392.2 12, 2, 22, N
i I \
\ H

N O

H

N~

'~ N,CHs N 2.38 392.2 12, 2, 22, ~ \ / CHs 56 \

I

F ~ N O

H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+hl]'" (Ex. No.) OH
F O~N -( ~ ~ / 2.98 446.0 336, 2, 22 I ~ N\ Hi N O
H

OH
OZN
N~ ~ N~ 2.98 446.0 336, 2, 22 H
I ~ ~ H O
F

H C~O 02N -' N~ ~ N 3.24 438.0 336, 2 H
N O
H

H3C.0 ~ I ~ N~ ~ N 3.24 438.0 336, 2 H
N O
H

N
O

1.90 385.3 319 F I \ N\
F N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]+ (Ex. No.) N

~
N ~ //-S
H

a N~ ~
~

N 2.75 444.0 12, 2, 22, \ N~ H i 21 a N O

H

N
S

/%
HaN

CHa ~ / N

N ~ ~ N CH 3.15 474.1 12, 2, 22, \ 21 I
\ H HC

N O

H

375 O~ H
N - // N
H

z \ / O
/ \

\ N~ ~ Nr 2.87 426.2 375 H

N O

H

N~ -CH3 HEN -i F 1.69 421.0 12, 2, 22 w H , I \

N O

H

~N-CH3 HaN

i N 1.69 421.0 12, 2, 22 \ , ~ H

F N O

H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]+ (Ex. No.) N
HEN
2.79 442.4 12, 2, 22, 56 F3C I \ Nw N~
H
N O
H

N
HEN
2.79 442.4 12, 2, 22, 56 \ N~ H
FCC H O

N
HEN
2.97 456.2 12, 2, 22, 56 F3C I \ N\
N O
H

N
HEN
2.97 456.2 12, 2, 22, 56 N~ H~

382 O /~
N~N~O
H2N ~ ~ CHs 2.14 515.3 12, 2, 22, 56 FsC I \ Nw N
H
N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]* (Ex. No.) _ ~--i ~o HzN CHs 2.14 515.3 12, 2, 22, 56 FsC I \ N\
N O
H

NU -~N CH3 HzN ~ ~ CHs 2.06 556.4 12, 2, 22, 56 FsC ~ \ N~ N
H
N O
H
385 °
NU -~ /_'CHs N
HzN ~ / ~-CHs 2.06 556.4 12, 2, 22, 56 N~ H
FsC ~ H O
386 O n N~
HZN
2.64 458.3 12, 2, 22, 56 \ N\ N~
H
N O
H

NV
HZN
2.64 458.3 12, 2, 22, 56 \ N\ H~

388 o H
N
~--S
HzN ~ // N/
\ N ~F3 3.61 472.1 12, 2, 22, 21 \ Nw Nr H
N O
H

Ex. LCMS LCMS Preparative No. Structure RT lon Methods) (min) [M+H]*(Ex. No.) N ~CH3 HzN - ~ N

I \ / ' N 2.94 440.2 12, 2, 22, '\ N\
~

I
H
a N O

H

O N

H2N - ~ N

I \ / ~ N 3,65 538.2 12, 2, 22, \ Nw N~

i H I

N O \

H

N CHs .

HZN - f N

I \ J ~N

\ N~ N~ 3.74 532.3 12, 2, 22, ~
H I

N o \

H

HaC CH

s N CHs .

~ N
HaN

\ / 3.26 476.2 12, 2, 22, I ' N 21 N~
~

N
i a I

N O \

H

N~ -CH3 HZN

I \ / 2.16 471.0 12, 2, 22, C
~ N\ N~

I
H

N O

H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]+ (Ex. No.) N~ -CH3 HZN
2.16 471.0 12, 2, 22, 56 ~ N~ H~

N ' HEN
F3C ~ N~ ~ N \ / i \ 2.26 507.1 12, 2, 22, 56 ~ H. N
N O
H

N
HEN
\ N\ ~ N \ / ~ \ 2.26 507.1 12, 2, 22, 56 H. N

\ /
N
p 3.15 558.2 12, 2, 22, 56 HEN -FsC I .~ N~ Hi N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) (M+H]* (Ex. No.) N
~N
p 3.15 558.2 12, 2, 22, 56 HZN -\ N~ H

N~~~, N,CH3 F C N zN ~ \ / CH3 2.15 485.2 12, 2, 22, 56 N.
H
N O
H

N~r~ N,CH3 N ZN ~ ~ / CH3 2.15 485.2 12, 2, 22, 56 N, H
FaC / H O
401 ~ -CH3 N

/ H3C 2.99 488.4 12, 2, 22, 56 F3C I \ N\
N O' H

Ex, LCMS LCMS Preparative No. Structure RT Ion Methods) (min) rM+H]+ (Ex. No.) 402 ~ -CHa O
N
H2N ~-CHs / HsC 2.99 488.4 12, 2, 22, 56 I ~ N~ ~i 403 /=N
N
N
O 2.75 535.1 12, 2, 22, 56 HzN -/
F3C I \ N\
N O
H
404 /=N
N
N
~N
O 2.75 535.1 12, 2, 22, 56 / o Nw H~

N
F HaN
2.97 468.3 336, 2, 22, 56 N\
N O
H

Ex. LCMS LCMS Preparative No. Structure RT lon Methods) (min) [M+H]+ (Ex. No.) \ /
N
~N
O 2.87 563.2 336, 2, 22, 56 HEN -/
FsC ~ ~ N~ H~
N O
H

\ /
N
'-N
O 2.87 563.2 12, 2, 22, 56 HzN -\ /
N\

N
F HEN
\ / 3.01 482.3 336, 2, 22, 56 N\
N O
H
409 r -CHs O
N

N ZN I \ / 2.75 486.9 336, 2, 22, 56 _H
N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+hl]+ (Ex. No.) 410 ~ -CH3 O
N
H
HzN '-2.64 446.2 12, 2, 22, 56 F3C \ N\ N/--H
N O
H
411 ~ -CH3 O
N
H
HZN
/ 2.64 446.2 12, 2, 22, 56 \ N~ Hi F3C ~ N O
H
412 ~ -CH3 O
N
HzN - CHs 2.82 474.2 12, 2, 22, 56 F3C \ N\ N/-H
N O
H
413 ~ -CH3 O
N
HzN '- ~CH3 2.82 474.2 12, 2, 22, 56 I \ N\ H ~

H
414 p N
HzN -'N 2.35 525.2 12, , F3c I \ N~ H~ ~ 22, 56 N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+Hl+ (Ex.
No.) N

\ ~ ~ 12, 2, I 2.35 525.2 22 ~ N
Y ~

~ N , I

O i 02N \ ~ 336, 2, 2.79 457.0 I
~

~ N~ 22 N

H

N O

H

OH

i 02N \ f 336, 2, 2.79 457.0 I
I
~

~ N~ 22 N
v ~
I
H

/
N O

H

O

O

H2N ~ ~ 3.38 403.3 418 I

W Nw N

H

N O

H

419 ~ CHz O

HzN '-/ 2.92 361.4 418 N\

N O

H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]+ (Ex. No.) O
HEN -2.79 359.3 418 \ N~ H~
a N O
H

O
HEN
2.57 335.3 418 \ N~ Hi a N O
H

N

t 12, 2, F3C \ N~ ~ N \ / ~ 2.87 486.2 22, 56 I / H. HsC
N O
H

N
HZN -t 12, 2, O 2.87 486.2 I \ N~ N~ H3~ 22, 56 H
FsC / H O

336, 2, \ I \ N~ ~ N~ 497.3 2.20 I / H 22, 56 N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]+ (Ex. No.) O
N
'--N 336, 2, O 2.33 541.5 22, 56 F HzN -I ~ \ I
I w Nw N~
H
N O
H
426 ~H3 O
N
~N~ 336, 2, O 2.33 541.5 22, 56 HzN
~. N.. H
I \ / H O
F
427 ~ -~H3 N
F HzN ~-cH3 336, 2, N ~ \ l H3o 2.99 514.9 NY 22, 56.
H
N O
H
428 ~ -CHs N\
HzN - I CH3 \ ~ H3c 336, 2, ,\--~ 2.99 514.9 N~ H 22, 56 H o F

Ex. LCMS LCMS Preparative No. Structure RT lon Methods) (min) [M+H]+ (Ex. No.) 429 ° n N~
F / H2N \ / 336, 2, 2.67 484.3 w I ~ N~ I N~ 22, 56 ~I /~ H
_N O
H

N~
HEN
\ / 336, 2, N\ I N~ 2.67 484.3 I H 22, 56 F
431 ~ -~H3 O
N
_ H
F ~ HZN \ / 2.69 472.4 336, 2, I ~ ~--~ 22, 56 \ N~ H
N O
H
432 ~ -CHs N
HaN CHs \\ // F 56 W Nw I N
aH
N O
H
433 ~ -CHs N
HaN CHa \ / ~~ 134 Nw I NY
H
N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) {min) [M+H]+ (Ex. No.) 434 ~ -CH3 O
N

N ~ \ / ~CH3 ~ 56 N o H
435 ~ -CH3 O O _N
, N~ H~
N O
H
436 ~ -CH3 O ~ _N
, 354, 134 1 W N.
a N O
H
437 ~ -CH3 O~-N

N I \ / ~CH3 354 N o H
438 / \
O -N
N
HzN - CH3 \ / F 56 \ N~ N, H
N O
H

Ex. LCMS LCMS Preparative No. Structure RT lon Methods) (min) [M+H]+ (Ex.
No.) 439 / \
O -N

N
, HzN \ 134 /
I
-NJ-' \ Nw H

N O

H

440 / \
O -N

N
, HzN O 56 \ /

N I
~H3 \ ~ N

H

N O

H

44'I ~ -CHI
O

N~CH3 HzN -F

\\ // 56 ~

F \ N\
N

H

N O

H

~
O

N~CH3 HzN CI
\ / 134 F
\ Nw N~

I
H

N O

H

~
O

N~CH3 HzN O

\ / ~

F N ~
N.

H

N O

H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+Hl+ (Ex.
No.) 444 ~ -CH3 O

N~CH3 HZN -F

~
N~

H

F N O

H

445 ~ -CH3 O

N-CH

s HEN -/ C~ 134 \ Nw H~

F N O

H

446 ~ -CH3 O

N~CH3 HEN -\ / O 56 N ~

F ~ N O

H

O

N
~N

HzN F

\ /

i ~ N~

H
a N O

H , Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) (M+H]+ (Ex.
No.) 448 ~H3 O

N
?N

N\
~

H

N O

H

O

N
'-N

HzN - O i ~ /

N I

\

I

N O

H

N
O

\ Nw H~

a N O

H

N

O

HzN - CI 134 \ N~ Hi a N O

H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]+ (Ex.
No.) N

O

~ /

N I

\ ~ N

I
H

N O

H

N
~

N

O

HEN ~ F 56 I ~ /

\ N~ H~
a N O

H

N
~~

N

O

HEN - O~ 134 r \ Nw H
a N O
H

N
' -N

O

~ /

N !
\

I

'~ N O

H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) (MPH]t (Ex.
No.) N

O

HzN \ / F 56 I

'w N\
N

H

N O

H

N

O

HzN \ / ~~ 134 ~

N\
N

H

N O

H

N

O

HzN O 56 \ /

N I

I

N O

H

N

O

HzN F 56 \ /

'w N\
~

I
H
a N O

H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) jM+H]+ (Ex.
No.) N

O

HzN - CI 134 /

\ N~ H

a N O
H

N

O

HzN O 56 \ /

N ~
\ \ N.

I
H

N O
H

>

O

\ /

l \ N~ Hi N O
H

>

O

HEN - O~ 160, \ / 134 \ N~ Hi a N O
H

Ex. LCMS LCMS Preparative No. Structure RT lon Methods) (min) (M+H]'"(Ex.
No.) O
>

O

HzN O 160 ~ /

N ~

I \

N O
H

N

N
'--N

HzN F

\ N~ Hi N O
H

y N

N
'-N

156, \ N~ Hi N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]+ (Ex.
No.) y N

N
'---N

HEN O
v /

cH3 \ Nw N~

a N O

H

468 -CHa ~
O

N

CHs \ N\

I

N O

H

N O

\ Nw H

a N O

H

N

\ Nw H~

N O

H

N

\ N~ Hf a N O

H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) jM+H]+ (Ex.
No.) 472 O !~

N\
~

H
a N O

H

473 O /-'~

~.%

~ ~J 21 N\ H

N O

H

474 O n NUJ

N
~ ~ 21 ~

Nw Hl-'r Hs I

N O

H

~N~
--~~
~/

N

N~ H~

N O

H

476 O N ' N~N/, N

N~ H

N O

H

Ex. LCMS LCMS Preparative No. Structure ~ RT Ion Methods) (min) (M+H)+(Ex.
No.) N~ \ / CN

\ /
~

N\ 21 N~

aH

N O
H

U \ ~ o I \ N.. H~

N O
H

N
-N
\ / \ /

~
~ N~

H
a N O
H

~
O

N
H

Nw H~

a N O

H

481 ~CH3 ~
O

N
\-CH

N~ H~

N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]+ (Ex. No.) 482 ~ -CH3 O
N
--CHs \ / H3C 21 W Nw ~ NY
H
N O
H

N
\ / 21 I ~ N~ H' ~N
a N

484 ~ ~ H

N
O
N
, /
N~ H~
a N O
H
485 N~ \
O
N

/
N\ H/
a N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]~ (Ex. No.) N
N,CH3 N' H~
a N O
H

N

N' NY
aH
N O
H

N
N ~ \ / O 21 I ~ w H, HsC
N O
H
489 H3C ~-O

N' ~ N~ \O 56 H
N O
H
490 H3c ~-o \ / S' p N\ ~ N~ O 354 aH
- N O
H
491 H3C, / \

\ / N
N' ~ N~ 'O 56 aH
N O
H

Ex. LCMS LCMS Preparative No. Structure RT lon Methods) (min) [M+ii]+(Ex.
No.) 492 H3C ~--O
N

HZN -~

F \ N~ I N 56 / O
H.

N O
H

N C

-HEN -\ N\ ~ Nr 'O 56 H

F ~ N O
H

HzN N

p 56 \ Nw N~
H

N O
H

495 ~ -CH3 ~N
<
' HEN
\ /

I
O
w. N\ N~

N O
H

496 CHs ~N
C
J

N
9 HzN

N
i I \
\ H
a N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+hl)'" (Ex. No.) I ~ ~ p 56 I \ N~ Ni H
N O
H

HZN - N
I ~ l O 56 \ N~ N~
H
N O
H

HEN -. O
I ~ ~ 160 \ N~ Hi a N O
H

N
HZN \ / 156 \ Nw I Nd-"
H
N O
H

HN
~O
HN
HEN \ / 156, 214 \ N~ I N/-' H
N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]+ (Ex. No.) N
HN
O
H ~ 156, 214 HEN -\ N~ H~
N O
H

H3 ~
N
~O
HN
156, 214 /
N~ N~
H
N O
H

O~NCHs ~O
HN
H2N - 156, 214 N\ H~
a N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]+ (Ex. No.) 505 ~ -CHI

N~ Hi N O
H

O.CN3 HZN \ /
~ N~ ~ N~ 49, 2, 3 ..N I / H
H3C ~O H O
507 HEN -' j \ /
N\ N~
H 13, 2, 3 ~N H O
HsC.N

HEN - i \ / HN O 319, 2, N~ NY/~ 151, 3 I ~ H HsC
N O
H
509 CH3 O /~\
N, ) \ / 21 ~ N~ H ~
a N O
H

Ex. LCMS LCMS Preparative No. Structure RT Ion Methods) (min) [M+H]'"(Ex.
No.) F N

HaN - N

\ N\ N~

H

N O

H

N

~

\ N~ H~ ~F

N O

H

N S

~J

F I \ N\

N O

H

N

O

N

HEN ~ H 56 \ N\

I

N O

H

*Preparative methods: the numbers in this column indicate the order in which the processes analogous to the numbered specific examples (described below) would be followed, to make the specific compound identified in the row.
Asymmetry, i.e., where a compound's mirror image cannot be super-imposed on the compound, may be present in a compound of Formula (I) due to the inherent structure of the molecule. Examples of such asymmetric molecules include certain allenyl compounds. The compounds of this invention may also contain one or more asymmetric centers depending upon the location and nature of the various substituents selected. A
molecule with a single asymmetric center may be a mixture of enantiomers (R,S), or may be a single (R) or (S) enantiomer. A molecule with more than one asymmetric center may be a mixture of diastereomers, or may be a single diastereomer.
Additionally, a compound may exhibit asymmetry due to restricted rotation about a given bond, for example, the central bond adjoining two substituted aromatic rings of the specified compound. It is intended that all such configurations and conformations (including enantiomers, diastereomers, and other optical isomers) are included within the scope of the present invention. Separated, pure or partially purified stereo isomers of the compounds of Formula (I) are each included within the scope of the present invention.
Preferred compounds are those with the absolute configuration or conformation which produces the more desirable biological activity.
The use of pharmaceutically acceptable salts of the compounds of this invention are also within the scope of this invention. The term "pharmaceutically acceptable salt"
refers to either inorganic or organic salts of a compound of the present invention that have properties acceptable for the therapeutic use intended. For example, see S. M.
Berge, et al. "Pharmaceutical Salts," J. Pharm. Sci. 1977, 66, 1-19.
Representative salts of the compounds of this invention include the conventional non-toxic salts and the quaternary ammonium salts that are formed, for example, from inorganic or organic acids or bases by means well known in the art. For example, such acid addition salts include acetate, adipate, alginate, ascorbate, aspartate, benzoate, benzenesulfonate, bisulfate, butyrate, citrate, camphorate, camphorsulfonate, cinnamate, cyclopentanepropionate, digluconate, dodecylsulfate, ethanesulfonate, fumarate, glucoheptanoate, glycerophosphate, hemisulfate, heptanoate, hexanoate, hydrochloride, hydrobromide, hydroiodide, 2-hydroxyethanesulfonate, itaconate, lactate, maleate, mandelate, methanesulfonate, 2-naphthalenesulfonate, nicotinate, nitrate, oxalate, pamoate, pectinate, persulfate, 3-phenylpropionate, picrate, pivalate, propionate, succinate, sulfonate, tartrate, thiocyanate, tosylate, and undecanoate. The term acid addition salts also comprises the hydrates and the solvent addition forms which the compounds of this invention are able to form. Examples of such forms are, for example, hydrates, alcoholates and the like.
Base salts include alkali metal salts such as potassium and sodium salts, alkaline earth metal salts such as calcium and magnesium salts, and ammonium salts with organic bases such as dicyclohexylamine and N-methyl-D-glucamine.
Additionally, basic nitrogen containing groups may be quaternized with such agents as lower alkyl halides such as methyl, ethyl, propyl, and butyl chlorides, bromides and iodides;
dialkyl sulfates including dimethyl, diethyl, and dibutyl sulfate; and diamyl sulfates, long chain halides such as decyl, lauryl, myristyl and strearyl chlorides, bromides and iodides, aralkyl halides including benzyl and phenethyl bromides, and others.
The esters of appropriate compounds of this invention are pharmaceutically acceptable esters such as alkyl esters, including methyl, ethyl, propyl, isopropyl, butyl, isobutyl or pentyl esters, and the like. Additional esters such as phenyl-(C~-C5) alkyl may be used, although methyl ester is preferred.
Unless the context clearly indicates to the contrary, whenever the term "compounds of this invention," "compounds of the present invention", and the like, are used herein, they are intended to include the chemically feasible pharmaceutically acceptable salts and/or esters as well as all stereoisomeric forms of the referenced compounds.
Method of making the compounds of the present invention In general, the compounds used in this invention may be prepared by standard techniques known in the art, by known processes analogous thereto, and/or by the processes described herein, using starting materials which are commercially available, producible according to routine, conventional chemical methods or the synthesis of which is described herein.
Generally, compounds of the Formula (I) where R3 is H, (C~-C4)alkyl, or OH, Formula (la) [where R3 is H], (Ib) [where R3 is N02], and (Ic) [where R3 is NH2], can be synthesized as shown in Scheme 1. Compounds of Formula (I) where R3 is OH
require the protection of the OH group prior to the first step; deprotection can occur during the third step. Compounds of Formula (I) where R3 is (C~-C4)alkyl are prepared from (la) where R3 is H by a three step procedure analogous to that of Zeitschrift fuer Naturforschung, Teil B: Anorganische Chemie, Organische Chemie, 30B(11-12), 954-8;
1975, that is incorporated herein by reference. Except for compounds where R~
or R2 is an optionally substituted amine or pyrrolidinyl (see Scheme 4), or where R3 is H and R4 is S(O)2R~ (see Scheme 11 ), treatment of a substituted indole of Formula (II) with a protecting group produces an N-protected indole of Formula (III). The compound of Formula (III) can then be deprotonated and quenched with an electrophile to furnish a dicarbonyl indole compound of Formula (IV). The Formula (IV) compound can be condensed with an aryl 1,2-diamine of Formula (V) to generate a compound of Formula (la). Nitration of the compound of Formula (la, where R3 is H) can provide the nitroindole compound of Formula (Ib) [where R3 is N02]. Reduction of the nitro functionality of the compound of Formula (Ib) can furnish a Formula (Ic) compound [where R3 is NH2].
Scheme 1 / I \~~ Rs Boc20 / I \~~ R5 1 ) t BuLi H~ ~ N
R12 Boc R12 2) (C02Me)2 (II) (III) where R3 = H or protected OH , R3 R11R4 Ar~ NH2 R3 -~=1 Rs O ~~ 2 ~H 1 ~ /
/ ~1 5 R 2 R N I ~--.( R (V) ~ N' 'R12 Me0 H~ ~ Ar ~ H
O R12 AcOH R2 N O
(IV) H (I, where R3 = H or OH

R
R3 -~~ R5 (la) 1.) Protect R1 I
N~ N~ ~R12 (I, where 2.) t-BuLi Ar ~ H
3_ ) 2 R - H 3.) (C1_C4)alkyl-halo R H O
(I, where R3 = (C1-C~)alkyl) isoamyl nitrite R11R4 (when R3 = H) 02N \ ~ ~ Rs R1 I ~--~
N~ N' 'R12 Ar C H
R N O
H (Ib) R11 Ra H2N -~1 Rs H2, Pd/C Ar ~N~ H ~R~2 or SnCl2 R2 N ~O
H (Ic) or FeIAcOH
Formula (II) is readily available, or see Scheme 15 (for synthesis of Formula II
where R4 is optionally substituted phenyl or optionally substituted pyridyl), Scheme 16 (for 117 ' synthesis of Boc protected Formula (II) [that is, Formula III] where R4 is (C~-C6)alkoxy -'-N X
optionally substitued with ' ~--~ ), Scheme 19 (for synthesis of Formula (II) where R4 is N[(C~-C3)alkyl]2,) and Scheme 21 (for synthesis of Formula (II) where R3 is H).
Ar Formula (V) is readily available or see Scheme 14, where substituted is Ar readily available as a di-nitro compound, or see Scheme 20 where substituted is readily available as a nitroaniline compound.
Compounds where R3 is NH(C~-C4)alkyl, NHC(O)(C~-C4)alkyl, or NHC(O)phenyl are synthesized starting with Formula (Ic), according to Scheme 5.
Reaction Schemes 2, 3, 5 through 10, 12 and 13 each describe how to make compounds with certain R4 sub-groups where the starting material is an R4-sub-group compound of Formula (la) [Scheme 8, which can be applied when R3 is H, as in Formula (la), or when R3 is alkyl], Formula (Ib) [Schemes 2, 3, 6, 7, 9,10, 12 and 13, which can be applied when R3 is NO2, or is H, or alkyl]. As stated previously, Formula (1c) from Reaction Scheme 1 (where R3 is NHS and R4 is as described without limitation) can be converted to a compound where R3 is NH(C~-C4)alkyl, NHC(O)(C~-C4)alkyl, or NHC(O)phenyl according to Scheme 5.

Scheme 2 shows how compounds of Formula (I), where R3 is N02 and R4 is CN, can be converted to compounds of Formula (I) where R4 is C(O)RE by standard functional group manipulation. For example, a cyanoindole (Id) can be hydrolyzed under basic conditions to an indole carboxylic acid (le). Coupling of acid (le) with an amine provides a variety of amides of general Formula (If).
Scheme 2 02N '-\CN 02N -~OH
i 5 1 ~ ~ / R5 1 I ~ R
Nw N~R12 K-~ R N~ N~R12 ArC H ArC H

H (Id) H (le) NH2R10, NH[(C1-C3)alkyl)]2, NH[(C1-C3)alkyl)]R8, R11 O
NH[C3-C6)cycloalkyl](C1-C3)alkyl, II
or 02N -~Rs an optionally substituted 1 I ~ ~R5 N ~ 12 morpholine, pyrrolidine, piperizine, or Ar ~ ~ H R
piperidine R N O
H (If) coupling agent, e.g., PyBOB or SOCI2 Other Formula (I) compounds where R~ is NO~, and R11 and R12 are both H, can be prepared by conversion ofi the acid (le) to the alcohol of Formula (Ig) by a two step procedure employing an imidazolyl carbonyl intermediate followed by reduction as shown in Scheme 3. Treatment of alcohol (Ig) with a halogenating agent such as SOBr2 produces a compound of Formula (Ih). Reaction of the halide (Ih) with either an alcohol or amine furnishes the ether (li) or the amine (Ij), respectively.
Scheme 3 H 1 ) CDI 02N \ ~OH

R 2) NaBH4 R Ar N~ N
Ar ~ ~~~ H

H (le) H (Ig) O2N ~Br 02N ~O(C1-C3)alkyl 1 ~ ~ / 1 1 \ /
SOBr2 R N r base R N
w N - w N
Ar ~ H {C1_C3)afkyl-OH 2 Ar ~ H

H {lh) H (li) an optionally substituted amine, e.g., an optionally substituted morpholine, NH[(C1-C3)alkyl]2, Ph-NH2, pyrolidine, piperazine, piperidine 02N -.~Y
1 \ / Where Y is an optionally substituted R N\ I NY amino group, e.g., morpolinyl, 2 Ar ~ H pyrolidinyl, piperizinyl, piperidinyl, R N O NHPh, or N[(C1-C3)alkyl]2 H (IJ) Compounds of Formula (lk) in which the Ar ring is benzo, R' or R2 is an amino substituent, and R3 is H can be prepared as shown in Scheme 4. Conversion of a difl~loronitrobenzene of Formula (V1) to an aniline of Formula (VII) is accomplished by ammonia displacement of a fluoronitrobenzene. Displacement of a second fluoro group from the compound of Formula (VII) by an amine of Formula (Vlf1) provides a phenylenediamine intermediate of Formula (IX). Reduction of the nitro group in (IX), followed by intramolecular condensation with ketoester (IV) provides a compound of Formula (Ik).
Scheme 4 N02 NH3 I ~ N02 \ N02 ---> / H-Y (VIII) (VI) (VII) (IX) R~~
O R4 ..
~~~ Rs Me0 ~N~
O H R~2 (IV) Y-'\~
--Fe, AcOH H (Ik) Y = an optionally substituted amine, e.g., an optionally substituted amine, HN[(C~-C3)alkyl]2, H2N[(C~-C3)alkyl], morpholine, piperarazine or pyrrolidine A compound of Formula (Ic) where R3 is NH2 can be alkylated or acylated to produce compounds of Formula (Im) as shown in Scheme 5.
Scheme 5 R3 -~R4 3 4 base + R JR
i) ~ ~ 5 R1 N ~ ~~RS (C1-C4)aIkyIC(O)CI R1 N I R2 N R12 Ar ~ N~R
Ar I H ~,L C H
2 or (C1-C~)alkyl-Br 2 N O
R N O R
H or phenylC(O)CI H
(Ic), where R3 = NH2 (Im), where R3 =
NHC(O)(C1-C4)alkyl, HN(C1-C4)alkyl, or NHC(O)phenyl Preparation of compounds of Formula (In), prepared using the method described in Scheme 2, where R3 is NQ2 and R4 is an amido substituted pyrrolidine amide is shown in Scheme 6. A pyrrolidine amide (In) can be converted to the primary amine derivative (lo), which can be acylated to provide the amide (Ip).
Scheme 6 R11 ~ R11 02N -~N 02N -~N
R1 N I ~ ~ acid R1 N
i \ . v N 12 ~ N R12 Ar ~ H R NHBoc Ar ~ H NH2 R2 N ~O R2 N O
H (In) H (lo) 02N -~ ~N
(C1-C3)aIkyIC(O)CI R1 N~ N \R12 NH
2 Ar C H O
R N O ~ 1-C3)alkyl H (Ip) Compounds of Formula (Iq) where R3 is N02 and R4 is an acylsulfonamide are prepared as shown in Scheme 7. The indole carboxylic acid (le) is reacted with a sulfonamide to produce a sulfonyl carboxamide (Iq).
Scheme 7 R11 ~ R11 O .
O N OH 2 -~.N~S02phenyl ON
1 I ~ ~ H2NS02phenyRl ~ ~ ~ H
R Ar I N H~R12 --~ N~ N~ ~R12 Ar ~ H
R2 N ~O R2 N O
H (le) H
Preparation of compounds of Formula (It) where R3 is H and R4 is a pyridyloxy group are shown in Scheme 8. A methoxyindole of Formula (Ir) can be transformed into a hydroxyindole (Is), then coupled with a halopyridine to provide a biaryl ether (It) as shown.
Scheme 8 R3 -~OMe Rs -,OI-R1 I ~ ~ BBr3 1 N\ N~R12 R N~ N~R12 Ar ~ H Ar ~ H
R2 N ~O R2 N O
H (Ir) H (Is) Ropt sub Cl (1r), (is), (lt): (i), where ~ ~ N
R3= H or (C1-C4)alkyl sub Ar R N
H (It) Other Formula (Iw) compounds where R3 is N02 and R4 is a urea substituted pyrrolidine amide can be prepared as shown in Scheme 9. A protected amine (lu, prepared using the method described in Scheme 2) can be reacted with TFA to produce an N methylamine of Formula (Iv). Secondary amine (Iv) can be converted to urea (Iw).
Scheme 9 02N _/~~N 02N _J-~~N
R I ~ ~ ~ TFA; 1 Ar I N H~R ,NHBOC NaHC03 R Ar ~ N R12 ~NH
HsC ~~~ H H C
R N O R2 N ~O s H (lu) H (Iv) 02N ~ ~1N
(C1-C3)alkyl-NCO R1 I ~ ~ H
----~ Ar N~ N ~R12 4N~N-(C1-C3)alkyl 2 ~~~ H H3 -~C
R N O O
H (lw) Other Formula (I) compounds where R3 is N02 and R4 is oxadiazole can be prepared by conversion of an amide of Formula (If) to the dehydrated heterocycle of Formula (Ix) as shown in Scheme 10.
Scheme 10 R11 ~ H p11 N-N
02N N.N~CH3 t Ha R1 N\ I N~ / 12H IOI P~05 R1 N
2 Ar ~ H ~R Ar , R N
H (If) H (Ix) Compounds of Formula (ly) can be prepared as shown in Scheme 11. For example, boronic acid indoles of Formula (X) can be united with an aryl chloride to provide indoles of Formula (XI). Acidic hydrolysis of aryl chlorides of Formula (XI) could produce quinoxalinones of Formula (ly).
Scheme 11 R11 O O R1 N CI R _ O~~O
- js\R7 Ar ~ ~ ~ ~S sR7 ~R

~--( N 12 Pd II R
(HO)2B N~R12 ( ) Ar C H

(X) (XI) R O\~O
.-~S.R~
AcOH R1 N\ N~---~RR
Ar ~ H

H (IY) Hydroxymethyl indoles of Formula (Ig) where R3 is N02 and R4 is hydroxymethyl can be reacted with an isocyanate to furnish carbamates of Formula (Iz) as shown in Scheme 12.
Scheme 12 02N ' ,~OH O2N - ,~O~N~Phenyl R1 ~ ~ /ERs 1 I ~ ~~Rs H
N\ N~R12 phenyl-NCO R N' N~R12 2 Ar C H Ar C H
R N O R2 N 'O
H (19) H (Iz) Compounds of Formula (1e) can be converted to acid chlorides of Formula (XII) and reacted with an alcohol to produce ester derivatives of Formula {laa) as shown in Scheme 13.
Scheme 13 02N ;> 'OH 02N ~Ci 1 ~ ~ ~ R5 SOCI2 1 ~ ~ f R5 R Nw N R12 R N~ N~R12 ArC H . ArC H
R N O R2 N ~O
H (le) H (XII) 02N .- /~O_Q
HO-Q R1 ~ ~ W R5 where, Q =
----~ Nw N~ ~R12 (C1-Cs)alkyl, 2 Ar ~ H (C3-Cs)alkenyl, R N O (C3-Cs)alkynyl, or H (laa) (C3-Cs)~Y~loalkyl Preparation of Intermediates Compounds of Formula (V), used in Scheme 1 above are either commercially available or can be prepared by reducing the appropriate 1,2-dinitroaryl precursor (X111) as shown in Scheme 14.
Scheme 14 Ar IC H2~ Pd/C Ar ~ NH2 z NO z ~ H
R (X111) ~ R (V) N 2 Biaryl indole compounds of Formula (Illb) where R4 is phenyl or pyridyl can be prepared as shown in Scheme 15. Performing a palladium catalyzed cross coupling between an indole boronic acid of Formula (Ilb) and an optionally substituted phenyl or pyridyl bromide to provide the indole of Formula (Ilc). Protection (Ilc) at the indole nitrogen provides the biaryl intermediate of Formula (Illb).
Scheme 15 R3 R~ ~ R3 R~ ~
/ I .~~ B(OH)2 Pd / I ~~ Z.-Ropt sub N ~~ s N ~~ s R ~ R
H R12 Ropt sub H R~2 (Ilb) Z~halo (Ilc) R3 R~~
BOC2O / ~ ~~_Z-R°Pt sub N ~~~ s R where Z is phenyl or pyridyl, Boc R~2 and R°Ptsub is an optional substituent (Illb) as defined above for R4 Intermediate indoles, used to prepare compounds of Formula (I), in which R4 is an morpholinyl-substituted alkoxy group, can be prepared from a hydroxyindole (Illc) as shown in Scheme 16. Conversion of (Illc) to an amine of Formula (Ille) is accomplished in two steps via an intermediate haloether (Illd). The Formula (Ille) indole is carried on to final product of Formula (I) in the Schemes described above.
Scheme 16 R3 R~ ~ R3 R~ ~ Br / \ OH Br~Br /
~J I ~~J
N \Rs N s Boc R~2 Boc R~2R
(Illc) (Illd) ~NH /
N~\RO
Boc R~2 (Ille) When substituted piperazine is used in the preparation of Formula (I) compounds in which R4 is an alkyl or acyl group substituted by piperazine, the substituted piperazine can be prepared by conversion of a compound of Formula (XIV) to a sulfonamide (XV) upon treatment with methylsulfonyl chloride. The product, a N Boc protected piperazine (XV) can be converted to a monosubstituted piperazine of Formula (XVI) by subjecting (XV) to an acid such as TFA as shown in Scheme 17. The resulting Formula (XVI) can be used, for example, in the last step in Scheme 2.

Scheme 17 HN~N-Boc - CH3S02-( ~N-Boc (XIV) (XV) acid CH3S02- ~NH
(XVl) Amine derivatives ofi Formula (XVIII) can be prepared by conversion of a ketone of Formula (XVII) via reductive amination as shown in Scheme 18. This Scheme, includes synthesis of the amine compounds that convert to N[(C3-C6)cycloalkyl][(C1-C3)alkyl] and to substituted N[C1-C4)alkyl]2, and can be inserted into, for example, the last step of Scheme 2, the last step to make Formula (Ij) in Scheme 3, and as compound (VIII) in Scheme 4.
Scheme 18 O
~ NaB(OAc)3H
(C1-C3)alkyl"(C1-C3)alkyl + (C1-C3)aIkyINH2 _ (XVII) AcOH, CH2CI2 HN~(C1-C3)afkyl where the alkyl groups are optionally substituted and the alkyl groups of (C1-C3)alkyl' \(C1-C3)alkyl (XVII) can be joined either through a (XVIII) carbon or heteroatom Compounds of Formula (Illf) can be prepared as shown in Scheme 19.
Conversion of a fluoronitrobenzene of Formula (XIX) to an aniline of Formula (XX) can be accomplished by displacement of the filuorine of (XIX). Nitroaniline (XX) can be converted to aminoindole (Illf).
Scheme 19 \ N02 5 ~ N02 [(C1-C3)alkylj2NH R i F / CH3 [(C1-C3)alkylj2N CH3 ( (XIX) H
H3C0 5 / N where alkyl groups can >---N(CH3)2 R ~ ~ ~ be optionally substituted H3C0 [(C1-C3)alkyl]2N ~
R'2 (Ild) Compounds of Formula (Vb) can be prepared as shown in Scheme 20. Palladium assisted coupling of a bromonitroaniline of Formula (XXI) with aryl boronic acids could provide arylnitroanilines of Formula (XII). Reduction of the nitro group could provide diamines of Formula (Vb).
Scheme 20 Br N02 phenyl N02 phenyl NH2 R2 I ~ phenylB(OH)2 R2p ~ P~ R2 I \
NH2 Pd(II) ~ NH2 ~ NH2 (XXI) (XXII) (Vb) (where phenyl can be optionally substituted) Compounds of Formula (Illg) can be synthesized from anilines of Formula (XXIII) as shown in Scheme 21. The anilines could be converted to diazonium salts of Formula (XXIV) followed by reduction to substituted phenyl hydrazines of Formula (XXV). The hydrazines can be converted to phenyl hydrazones of Formula (XXVI) which can undergo an acid assisted cyclization to yield substituted indoles of Formula (Illg).
Scheme 21 R4 HONG ~ ~ j R4 Na2S03 ~ j R~
H2N ~ N2 ~ HN

(XXII I) (XXIV) (XXV) HsC~H> ~ i R4 H2~ / ~ s Ra HN N
HOAc H
(XXVI) (Ile) It is to be understood that sensitive or reactive substituents attached to intermediates or to compounds of Formula (I) may need to be protected and deprotected during the preparations described above. Protecting groups in general may be added and removed by conventional methods well known in the art [see, e.g., T. W.
Greene and P.G.M. Wuts, Protective Groups in Organic Synthesis; Wiley: New York, (1999)].
In addition, it is to be understood that reaction conditions for N- or O-acylation, alkylation, or sulfonylation of the intermediates and of Formula (I) compounds using acyl halides, alkyl halides and sulfonyl halides, respectively, and a suitable base, are generally interchangeable, as is well known in the art. For example, conditions to effect N-acylation as described in any of the specific examples below can also be used to effect N-sulfonylation by substituting the appropriate sulfonyl halide for the acyl halide.
The following specific examples are presented to illustrate the invention described herein, but should not be construed as limiting the scope of the invention in any way.
Abbreviations and Acronyms When the following abbreviations are used throughout the disclosure, they have the following meaning:
AcCI acetyl chloride AcOH acetic acid Boc t-butoxycarbonyl CDI carbonyl diimidazole Celite~ registered trademark of Celite Corp. brand of diatomaceous earth DMAP 4-(N,N dimethyl)amino pyridine DME dimethoxyethane DMF N,N-dimethyl formamide DMSO-ds dimethylsulfoxide-ds ESI electrospray ionization EtOAc ethyl acetate EtOH ethanol 'H NMR proton nuclear magnetic resonance Hex hexanes HPLC high performance liquid chromatography LCMS liquid chromatography / mass spectroscopy MeOH methanol MS mass spectrometry Pd/C palladium on carbon Rf TLC retention factor rt room temperature RT retention time (HPLC) TBDMS tent-butyldimethylsilyl TBDMSCI tert butyldimethylsilyl chloride TFA trifluoroacetic acid TH F tetrahydrofuran TLC thin layer chromatography TMS tetramethylsilane General Experimental Procedures Electron impact mass spectra (EI-MS) were obtained with a Hewlett Packard 5989A mass spectrometer equipped with a Hewlett Packard 5890 Gas Chromatograph with a J & W DB-5 column (0.25 uM coating; 30 m x 0.25 mm). The ion source was maintained at 250 °C and spectra were scanned from 50-800 amu at 2 sec per scan.
High pressure liquid chromatography-electrospray mass spectra (LC-MS) were obtained using either a:
(A) Hewlett-Packard 1100 HPLC equipped with a quaternary pump, a variable wavelength detector set at 254 nm, a YMC pro C-18 column (2 x 23 mm, 120A), and a Finnigan LCQ ion trap mass spectrometer with electrospray ionization. Spectra were scanned from 120-1200 amu using a variable ion time according to the number of ions in the source. The eluents were A: 2% acetonitrile in water with 0.02% TFA and B:
2% water in acetonitrile with 0.018°I° TFA. Gradient elution from 10% B
to 95% over 3.5 minutes at a flowrate of 1.0 mL/min was used with an initial hold of 0.5 minutes and a final hold at 95% B of 0.5 minutes. Total run time was 6.5 minutes.
or (B) Gilson HPLC system equipped with two Gilson 306 pumps, a Gilson 215 Autosampler, a Gilson diode array detector, a YMC Pro C-18 column (2 x 23mm, 120 A), and a Micromass LCZ single quadrupole mass spectrometer with z-spray electrospray ionization. Spectra were scanned from 120-800 amu over 1.5 seconds. ELSD
(Evaporative Light Scattering Detector) data was also acquired as an analog channel.
The eluents were A: 2% acetonitrile in water with 0.02% TFA and B: 2% water in acetonitrile with 0.018% TFA. Gradient elution from 10% B to 90% over 3.5 minutes at a flowrate of 1.5 mL/min was used with an initial hold of 0.5 minutes and a final hold at 90%
B of 0.5 minutes. Total run time was 4.8 minutes. An extra switching valve was used for column switching and regeneration.
Routine one-dimensional NMR spectroscopy was performed on 300 MHz Varian Mercury-plus spectrometers. The samples were dissolved in deuterated solvents obtained from Cambridge Isotope Labs, and transferred to 5mm ID Wilmad NMR
tubes.
The spectra were acquired at 293 K. The chemical shifts were recorded on the ppm scale and were referenced to the appropriate solvent signals, such as 2.49 ppm for DMSO-ds, 1.93 ppm for CD3CN, 3.30 ppm for CD30D, 5.32 ppm for CD2CI2 and 7.26 ppm for CDCI3 for ~H spectra, and 39.5 ppm for DMSO-ds, 1.3 ppm for CD3CN, 49.0 ppm for CD30D, 53.8 ppm for CD2CI2 and 77.0 ppm for CDCI3 for ~3C spectra.
Example 1 Preparation of 3-(1H-indol-2-yl)-2(1H)-quinoxalinone N~ H
a N O
H
Step 1. Preparation of tern butyl 2-fmethoxY(oxo)acetyl]-1H-indole-1-carboxylate O
O
N O
O\ /CH3 H CrCH3 In a 250 mL round-bottom flask was placed 2.0 g (9.21 mmol, 1 equiv) of N Boc indole in 40 mL of THF. The mixture was cooled to -78 °C and 1.1 equiv (6.33 mL, 1.6 M
in pentane) of t-BuLi was added dropwise. The mixture was allowed to stir for 30 min and 2.17 g (18.4 mmol, 2 equiv) of dimethyl oxalate in 20 mL THF was added quickly in one portion. The reaction was then allowed to warm to rt. After 30 min the reaction appeared to be complete by TLC. The mixture was diluted with 50 mL of water and transferred to a separatory funnel where it was extracted with EtOAc (3 x 200 mL). The combined organics were dried (Na2S04), filtered, and evaporated. The residue was then purified via flash chromatography (15% EtOAc/Hex) to provide 2.02 g (72%) of the desired product as a yellow oil. ~H-NMR (CD3CN) 8 8.06 (d, 1 H), 7.75 (d, 1 H), 7.55 (d, 1 H), 7.37 (d, 1 H), 7.32 9S, 1 H), 3.87 (s, 3H), 1.67 (s, 9H).
Stea 2. Preparation of 3-(1H-indol-2-LrIL(1H)-quinoxalinone N\
I~
N O
H
In a 25 mL round-bottom flask was placed 300 mg (0.99 mmol, 1 equiv) of tert-butyl 2-[methoxy(oxo)acetyl]-1H-indole-1-carboxylate and 118 mg (1.09 mmol, 1.1 equiv) 1,2-phenylenediamine in 10 mL of acetic acid. The flask was equipped with a reflux condenser and heated at 130 °C for 2 h. At this point, 1 mL of TFA was added to ensure complete removal of the Boc group. The mixture was then allowed to cool to room temperature and diluted with 10 mL of water. The resulting precipitate was filtered and rinsed with an additional 20 mL of water to provide 199 mg (77°I°) of the desired product as an orange solid. 'H-NMR (DMSO-d6) 8 12.62 (s, 1 H), 11.61 (s, 1 H), 7.86 (s, 1 H), 7.83 (d, 1 H), 7.65 (d, 1 H), 7.54 (d, 1 H), 7.50 (d, 1 H), 7.36 (t, 1 H), 7.35 (t, 1 H), 7.20 (t, 1 H), 7.02 (t, 1 H); LCMS RT = 2.96 min; [M+H]+ = 262.23.
Example 2 Preparation of 3~,3-vitro-1H-indol-2-yl)-2(1H)-auinoxalinone W N~ H
a N O
H
In a 100 mL round-bottom flask equipped with a reflux condenser was placed 3-(1H-indol-2-yl)-2(11-x-quinoxalinone (Example 1, 400 mg, 1.53 mmol) in 30 mL
of benzene and 6 mL of DMF. The mixture was heated to 100 °C and 538 mg (4.59 mmol, 3 equiv) of isoamyl nitrite was added. After 2 h, the reaction appeared complete and was allowed to cool to rt. The solvents were removed in vacuo and the residue suspended in CH3CN and sonicated. The remaining solids were filtered to provide 404 mg (86°I°) of the desired product as yellow solid. 'H-NMR (DMSO-d6) 813.15 (s, 1 H), 12.84 (s, 1 H), 8.12-8.08 (m, 1 H), 7.89 (d, 1 H), 7.69-7.59 (m, 2H), 7.45-7.37 (m, 4H); LCMS RT =
2.86 min;
[M+H]~ = 307.22.
Example 3 Preparation of 3 ~3-amino-1H-indol-2-yl~~1H)-auinoxalinone N\
N O
H
In a 25 mL round-bottom flask was placed 10 mg of 10% Pd/C under argon. To this was added 5 mL of THF. To this mixture was added 100 mg (0.33 mmol) of 3-(3-nitro-1H-indol-2-yl)-2(1H)-quinoxalinone (Example 2) as a solution in 3 mL of DMF and 5 mL of THF. The atmosphere was converted to one of H2 with a balloon and the reaction allowed to stir at rt for 1 h. The H2 was then removed and the mixture filtered through Celite~ under a blanket of argon. The solvents were then removed to provide 71 mg (78%) of the desired product as a red solid. ~H-NMR (DMSO-d6) 8 12.39 (s, 1 H), 10.57 (s, 1 H), 7.78 (d, 1 H), 7.72 (d, 1 H), 7.44 (d, 1 H), 7.28 (d, 1 H), 7.23 (t, 2H), 7.16 (t, 1 H), 7.02 (br s, 2H), 6.88 (t, 1H); LCMS RT= 2.33 min; [M+H]+= 277.28.
Example 12 Preparation of 6,7-dimethox -,~3-(5-cyano-1H-indol-2-yl~(1H)-guinoxalinone N
Me0 Me0 iv a H
Step 1. Preparation of tent-butyl 5-cyano-1H-indole-1-carboxylate NC
N
O\ /CH3 H C~CH3 In a 100 mL round-bottom flask was placed 1H-indole-5-carbonitrile (2.0 g, 14.07 mmol) in 20 mL of anhydrous THF. To this solution was added DMAP (0.86 g, 7.03 mmol) and the mixture was allowed to stir for 0.5 h at rt. At this point, Boc20 (3.07 g, 14.07 mmol) was added and the reaction stirred for an additional 2 h. The reaction was then quenched with water and extracted twice with ethyl ether. The combined organic layers were washed successively with 1 N HCI, water, and brine, then dried over MgS04 and concentrated to provide 3.26 g (96%) of the desired product as a white solid. 'H-NMR (DMSO-d6) 8 8.20-8.14 (m, 2H), 7.83 (d, 1 H), 7.70 (d, 1 H), 6.80 (d, 1 H), 1.63 (s, 9H).
Step 2. Preparation of meth rl 5-cyano-1 H-indol-2- r~l (oxo acetate O
NC ~ O
N
H
In a 100 mL round-bottom flask was placed 2.0 g (8.26 mmol, 1 equiv) of tent-butyl 5-cyano-1H-indole-1-carboxylate (step 1) in 25 mL of THF. The mixture was cooled to -78 °C and 1.1 equiv (5.34 mL, 1.7 M in pentane) of t BuLi was added dropwise. The mixture was allowed to stir for 1 h and 2.14 g (18.16 mmol, 2.2 equiv) of dimethyl oxalate in 5 mL of THF was added quickly in one portion. The reaction was then allowed to warm to 0 °C and stirred until complete, as monitored by TLC (about 2 h).
The mixture as diluted with 30 mL of water and transferred to a separatory funnel where it was extracted with EtOAc (3 x 100 mL). The combined organic extract was washed with brine, dried (Na2S04), filtered, and evaporated to give a brown residue. To the residue was added MeOH (10 mL) to give an insoluble yellow solid, which was filtered, washed with MeOH, dried, and purified to provide 444.3 mg (23.6%) of the desired product as a yellow solid.
'H-NMR (DMSO-ds) & 12.63 (s, 1 H), 8.40 (s, 1 H), 7.77 (s, 1 H), 7.65 (d, 1 H), 7.60 (d, 1 H), 3.93 (s, 3H).
Step 3. Preparation: 6,7-dimethox r-~3-(5-cyano-1 H-indol-2- rl ~1 H)-auinoxalinone CN
Me0 MeO
In a 25 mL round-bottom flask was placed 114.1 mg (0.50 mmol, 1 equiv) of 5-cyano-2-[methoxy(oxo)acetyl]-1H-indole (step 2) and 132.6 mg of 1,2-diamino-4,5-dimethoxybenzene hydrochloride (0.55 mmol, 1.1 equiv) in 5 mL of acetic acid.
The flask was equipped with a reflux condenser and heated at 130 °C for 3 h. The mixture was then allowed to cool to room temperature and diluted with 5 mL of water. The resulting precipitate was filtered and rinsed with an additional 10 mL of water, 5 mL of MeCN, dried in an oven to provide 127.1 mg (73.4%) of the desired product as a yellow solid. ~H-NMR
(DMSO-d6) 8 12.67 (s, 1 H), 12.08 (s, 1 H), 8.20 (s, 1 H), 7.80 (s, 1 H), 7.65 (d, 1 H), 7.49 (d, 1 H), 7.27 (s, 1 H), 6.85 (s, 1 H), 3.87 (s, 6H); LCMS RT = 2.68 min; [M+H]+
=.347.2.
Example 13 Preparation of 6-[S3S)-~dimeth I~oLpyrrolidinyll-3-(1H-indol-2-y~~1H~
a~uinoxalinone H3C, HC N ~ \ N\ H

N O
H
Step 1. Preparation of 5-fluoro-2-nitroaniline O~N
HEN F

The compound was prepared as described in WO 02/22598. To a round bottom flask equipped with a dry ice condenser (acetone/dry ice) was added 2,4-difluoronitrobenzene (15 g, 94 mmol) and THF (20 mL). Ammonia was bubbled into the solution for 10 min at -78 °C. The reaction was allowed to warm to room temperature and the reaction refluxed for 7 h. Stirring was continued overnight allowing the ammonia to evaporate after the condenser was removed. The reaction was diluted with dichloromethane and washed with water (3 x 100 mL). the organic layer was dried over MgS04, filtered, and concentrated under reduced pressure to yield a solid. The solid was purified by chromatography to afford 10.5 g (72%) of 5-fluoro-2-nitroaniline.
~H NMR
(DMSO-d6): 8 6.38-6.52 (m, 1 H), 6.66-6.72 (d, 1 H), 7.79 (s, 2H), 7.98-8.09 (dd, 1 H).
LRMS RT = 2.48; [M+H] = 157.
Step 2. Preparation of (3S- )-1_(3-amino-4-nitrophenyl)-N N dimethyl-3-pyrrolidinamine ~4 The compound was prepared as described in WO 02122598. To a round bottom flask equipped with a reflux condenser was added 5-fluoro-2-nitroaniline (4 g., 26.0 mmol) in 1-methyl-2-pyrrofidine (40 mL). (3S)-N,N-dimethyl-3-pyrrolidinamine (5.85 g., 51.2 mmol) was added to the stirring solution and the reaction was heated to 80 °C for 3 h. After cooling to room temperature, the reaction was poured over ice water.
The product was diluted with dichlorometliane and washed with saturated sodium bicarbonate (3 x 100 mL). The organic layer was dried with MgS04, filtered, and concentrated under reduced pressure to afford a solid. The product was purified by chromatography to yield 4.7 g (74%) of (3S)-1-(3-amino-4-nitrophenyl)-N,N dimethyl-3-pyrrolidinamine.
~H NMR
(DMSO-ds): b 1.81-1.92 (m, 1 H), 2.02-2.13 (m, 7H), 2.87-2.91 (m, 1 H), 3.06-3.16 (t, 1 H), 3.22-3.33 (m, 1 H), 3.41-3.8 (dt, 2H), 5.80 (s, 1 H), 6.00-6.14 (dd, 1 H), 7.25 (s, 2H), 7.75-7.83 (dd, 1 H). LRMS RT = 0.25; [M+H] = 251.
Step 3. Preparation of 6-[S3S~dimethylamino -1-pyrrolidin r1-~1H-indol-2-yl)-2(1H~
auinoxalinone H3C I / H.
H3C N ~N ~ Nw ) N
N O
H

The compound was prepared by reaction of the product prepared in Example 13, step 2, with the product of Example 1, step 1, using the method described for Example 49-50 step 2. 'H-NMR (DMSO-d6) b 12.25 (s, 1 H), 11.41 (s, 1 H), 7.65-7.51 (m, 3H), 7.58-7.49 (d, 1 H), 7.22-7.18 (m, 1 H), 7.16-7.01 (m, 1 H), 6.80-6.72 (d, 1 H), 6.38 (s, 1 H), 3.67-3.52 (m, 2H), 3.24-3.14 (t, 1 H), 2.97-2.81 (m, 1 H), 2.35 (s, 6H), 1.99-1.83 (m, 1 H). LCMS
RT= 2.06 min; [M+H]= 374.
Example 18 Preparation of 3-15-f3-(1-piperazi~l)propoxyl-1H-indol-2-y1~2j1H~guinoxalinone ~O
O~NJ
i ~ N~ N~
H
N O
H
Step 1. Preparation of tent-butyl 5-~droxy-1H indole-1-carboxylate HO
N

H3C-~--O~O

Tert-butyl 5-(benzyloxy)-1 H-indole-1-carboxylate (5.75 g, 17.8 mmol), prepared according to the procedure described for Example 12, step 1, was added to a mixture of 10% Pd/C in EtOH.
Ammonium formate was added and the reaction stirred for 6 h. The mixture was filtered through Celite~ under a blanket of argon and the solvents were then removed. The residue was purified by flash chromatography to yield 3.5 g of tent butyl 5-hydroxy-1H indole-1-carboxylate (74%). ~H-NMR
(DMSO-ds) 8 9.19 (s, 1 H), 7.84-7.78 (d, 1 H), 7.58-7.52 (d, 1 H), 6.91 (s, 1 H), 7.78-7.69 (m, 1 H), 6.65-6.42 (m, 1 H), 1.68-1.59 (s, 9H).
Step 2. Preparation of tern butyl 5-(3-bromopropoxlr)-1H indole-1-carboxylate Br O
N
H3C ~O
HH C~ /O

In a 250 mL flask was placed tart-butyl 5-(benzyloxy)-1H-indole-1-carboxylate (3.3 g, 14 mmol) in 100 mL of acetone. 1,3-Dibromopropane (5.74 mL, 56.6 mmol) was added, followed by cesium carbonate (5.5 g, 17 mmol). The reaction was heated to reflux for 5 h. The reaction was cooled to room temperature and diluted with water (200 mL).
The mixture was transferred to a separatory funnel and extracted with ethyl acetate (2 x 150 mL). The combined organics were dried (MgS04), filtered, and evaporated.
The residue was then purified via flash chromatography to provide 4.7 g of tart butyl 5-(3-bromopropoxy)-1H indole-1-carboxylate (94%). 'H-NMR (DMSO-d6) 8 7.99-7.89 (d, 1H), 7.61 (s, 1 H), 7.17 (s, 1 H), 6.98-6.91 (d, 1 H), 6.62 (s, 1 H), 4.16-4.05 (t, 2H), 3.64 (t, 2H), 2.37-2.20 (m, 2H). LCMS RT= 3.55 min; [M]+= 254.1.
Step 3. Preparation of tart buyl 5-f3-(4-mor~holinlrl)pro~~ox~l-1H indole-1-carbox I
O
~N
O
N
HaC O

In a 250 mL flask was placed tart butyl 5-(3-bromopropoxy)-1H-indole-1-carboxylate (1.5 g, 4.2 mmol) in 50 mL of tetrahydrofuran. Morpholine (0.41 mL, 4.66 mmol) was added, followed by pyridine (0.38 mL, 4.66 mmol). The reaction was heated to reflux for 5 h. The reaction was cooled to room temperature and diluted with water (200 mL). The mixture was transferred to a separatory funnel and extracted with ethyl acetate (2 x 100 mL). The combined organics were dried (MgS04), filtered, and evaporated. The residue was then purified via flash chromatography to provide 1.1 g of tart-butyl 5-[3-(morpholinyl)propoxy)-1H-indole-1-carboxylate (72%). 'H-NMR
(DMSO-d6) 8 7.93-7.85 (d, 1 H), 7.59 (s, 1 H), 7.09 (s, 1 H), 6.93-6.85 (m, 1 H), 6.59 (s, 1 H), 4.06-3.97 (t, 2H), 3.57 (s, 4H), 2.46-2.23 (m, 6H), 1.92-1.83 (m, 2H), 1.62 (s, 9H).
LCMS RT= 0.61 min; [M+H]+= 361.3.

Step 4. Preparation of tert-butyl 2-fmethoxy(oxo)ace~ll- 5 j3~- 4-mor holinyl)propoxy~-1H-indole-1-carboxylate O
~N

O
O \ ~ O
N O
H3C ~O
HsC-7"O

The compound was prepared by the method described for Example 1, step 1, using the product of Example 18, step 3 and dimethyl oxalate as starting materials. 'H-NMR (DMSO-ds) 8 7.86-7.80 (d, 1 H), 7.38 (s, 1 H), 7.20-7.29 (m, 1 H), 7.18-7.10 (d, 1 H), 4.06-3.99 (t, 2H), 3.80 (s, 3H), 3.57 (s, 4H), 2.47-2.24 (m, 6H), 1.96-1.83 (m, 2H), 1.59 (s, 9H).
Step 5. Preparation of 3-~5-f3- 1-~~iperazinyl~prol.~o~l-1H-indol-2-yl'~-2(1N~,c~uinoxalinone ~O
O~NJ
\ Nw N~
H
N O
H
The compound was prepared by the method described for Example 1, step 2, using the product of Example 18, step 4 and 1,2-phenylenediamine as starting materials.
'H-NMR (DMSO-d6) 8 12.59 (s, 1 H), 11.43 (s, 1 H), 7.82-7.78 (d, 1 H), 7.72 (s, 1 H), 7.55-7.47 (m, 1 H), 7.42-7.39 (m, 1 H), 7.37-7.29 (m, 2H), 7.13 (s, 1 H), 6.87-6.81 (m, 1 H), 4.08-3.98 (t, 2H), 3.57 (s, 4H), 2.46-2.23 (m, 6H), 1.97-1.81 (m, 2H). LCMS RT=
2.45 min;
[M+H] = 405.

Example 21 Preparation of N f3-(4-morpholinyllpropyll-2-(3-oxo-3 4-dihydro-2-quinoxalinyl~ 1H-indole 5-carboxamide n N O
IV V
H
In a 20 mL amber vial was placed 2-(3-oxo-3,4-dihydro-2-quinoxalinyl)-1H-indole-5-carboxylic acid (Example 17, 75.0 mg, 0.25 mmol, and 0.10 mL (0.74 mmol) of TEA in 3 mL of THF and 3 mL of DMF. To this was added PyBOP (39.0 mg, 0.27 mmol) and 3-(4-morpholinyl)propylamine (0.04 mL, 0.27 mmol) and the reaction allowed to stir at rt. After 45 min, the volatiles were removed and the residue purified via preparative HPLC
(CH3CN/H20 0.1 % TFA). The desired fractions were combined and the CH3CN
removed in vacuo. The remaining aqueous solution was basified with saturated NaHC03 and extracted with EtOAc (3x150 mL). The combined organics were dried (Na2S04), filtered, and evaporated. The residue was suspended in CH3CN, sonicated, and the solids filtered to provide 23 mg (21%) of the desired product as a yellow solid. 'H-NMR (DMSO-d6) 8 12.64 (s, 1 H), 11.84 (s, 1 H), 8.38 (t, 1 H), 8.17 (s, 1 H), 7.90 (s, 1 H), 7.83 (d, 1 H), 7.70 (d, 1 H), 7.52 (dd, 2H), 7.37-7.32 (m, 2H), 3.57 (t, 4H), 3.30 (m, 2H), 2.40-2.31 (m, 6H), 1.70 (quint, 2H); LCMS RT = 2.30 min; [M+H]+ = 432.29.
Example 22 Preparation of 3-nitro-2-(3-oxo-3.4-dihydro-2-auinoxalin~)-1 H-indole-5-carboxylic acid OH
IV V
H
!n a 15 mL round-bottom flask with condenser was placed 3-nitro-2-(3-oxo-3,4-dihydro-2-quinoxalinyl)-1 H-indole-5-carbonitrile (Example 19, 52.0 mg, 0.16 mmol) in 6 mL of 4 M
KOH. The mixture was heated at 120 °C for 3 h. At this point, the reaction was allowed to cool to rt and acidified with conc. HCI. The solids were filtered and dried in vacuo at 60 °C to provide 52 mg (95%) of the desired product as a yellow solid. ~H-NMR (DMSO-d6) 8 13.43 (s, 1 H), 12.99 (br s, 1 H), 12.90 (s, 1 H), 8.73 (s, 1 H), 7.98 (d, 1 H), 7.90 (d, 1 H), 7.70 (d, 1 H), 7.66 (d, 1 H), 7.40 (dd, 2H); LCMS RT = 2.58 min; [M+H]+ =
351.26.
Examples 49-50 Precaration of 3-(1H-indol-2-yl -6-f3- 4-morphlin 'propoxy~-2(1H~guinoxalinone and 3 (1H-indol-2-yl)-7-[3~- 4-morphlinyl)propoxy]-2(1H~auinoxalinone O
~N CN
NCO O I ~ N~ H~
OJ

Stea 1. Preparation of 5-f3-(4-morpholin~rl)propoxyl-2-nitroaniline O I ~ NHZ

5-[3-(4-morpholinyl)propoxy]-2-nitroaniline (706 mg g, 69%) was obtained in two steps by O-alkylation of 3-amino-4-nitrophenol (1.0 g, 3.6 mmof) with 1,3-dibromopropane, catalyzed by Cs2C03, followed by N alkylation of morpholine catalyzed by pyridine:'H-NMR (DMSO-ds) 8 7.36 (s, 1H), 7.25 (s, 2H), 7.17-7.09 (m, 1H), 6.97-6.88 (d, 1H), 3.98-3.84 (t, 2H), 3.56 (s, 4H), 2.50-2.22 (m, 6H), 1.85-1.78 (m, 2H). LCMS RT=
0.25 min; [M+H]+= 282.3.

Step 2. Preaaration of 3-(1H-indol-2-Lrl)-6-f3-(4-morphlinyl propoxY]-2~1H~-auinoxalinone and 3-(1H-indol-2-yl)-7-f3-(4-morphlinyl propoxyl-2(1~-g_uinoxalinone O
~N CN
N~./~O O I W N\ H~
OJ H O

In a 25 mL round-bottom flask was placed methyl (5-cyano-1H-indol-2-yl)(oxo)acetate (255 mg, 0.79 mmol, Example 12, step 2) and 219 mg (0.79 mmol) of 5-[3-(4-morpholinyl)propoxy]-2-nitroaniline (from step 1) in 10 mL of acetic acid, followed by iron powder (219 mg). The flask was equipped with a reflux condenser and heated at 130 °C for 2 h. The mixture was then allowed to cool to room temperature and diluted with 80 mL of diethyl ether. The resulting precipitate was filtered and dissolved in water (100 mL) and EtOAc/MeOH (100 mL, 10 mL). The organic layer separated and the aqueous layer was extracted two times with EtOAc/MeOH (100 mL, 10 mL). The organic extracts were combined and dried with MgS04. Filtration and concentrated under reduced pressure afforded a residue. The two regioisomers were separated by flash chromatography (30% EtOAc/5% MeOH/Hex) yielding 45 mg of 3-(1H-indol-2-yl)-7-[3-(4-morphlinyl)propoxy]-2(1H)-quinoxalinone (Example 49, 17%) and 15 mg of 3-(1H-indol-2-yl)-6-[3-(4-morphlinyl)propoxy]-2(1H)-quinoxalinone (Example 50, 5%).
Example 49, 3-(1H-Indol-2-yl)-7-[3-(4-morphlinyl)propoxy]-2(1H)-quinoxalinone:
~H-NMR (DMSO-d6) 8 12.61 (s, 1 H), 12.09 (s, 1 H), 8.21 (s, 1 H), 7.88 (s, 1 H), 7.65-7.60 (d, 1 H), 7.57-7.47 (d, 1 H), 7.37-7.22 (m, 2H), 7.20-7.16 (m, 1 H), 4.14-4.01 (t, 2H), 3.55 (s, 1 H), 2.58-2.20 (m, 6H), 1.97-1.81 (t, 2H); LCMS RT = 2.11 min; [M+H]~ =
430.2.
Example 50, 3-(1H-Indol-2-yl)-7-(3-(4-morphlinyl)propoxy]-2(1H)-quinoxalinone;
~H-NMR (DMSO-d6) b 12.61 (s, 1 H), 12.09 (s, 1 H), 8.21 (s, 1 H), 7.82 (s, 1 H), 7.78-7.73 (d, 1 H), 7.64-7.58 (d, 1 H), 7.52-7.43 (d, 1 H), 6.98-6.91 (d, 1 H), 6.79 (s, 1 H), 4.14-4.01 (t, 2H), 3.55 (s, 1H), 2.58-2.20 (m, 6H), 1.97-1.81 (m, 2H); LCMS RT = 2.21 min;
[M+H]+ _ 430.2.

Example 56 3-amino-2-(3-oxo-3 4-dihydro-auinoxalin-2-yl)-1H-indole-5-carbolic acid (2-methox -~~)-methyl-amide O
N

N~ H~
a N O
H
In a 500 mL round bottomed flask was placed 3-nitro-2-(3-oxo-3,4-dihydro-2-quinoxalinyl)-1 H-indole-5-carboxylic acid (3.77 g, 10.8 mmol, 1 equiv, Example 22) in 250 mL of DMF To this was added 1.65 mL of triethylamine (11.8 mmol, 1.1 equiv).
Upon dissolution of all solids, 6.16 g (11.8 mmol, 1.1 equiv) of PyBOP~ was added.
After stirring for 5 minutes at room temperature, (2-methoxy-ethyl)-methyl-amine (1.06 g, 11.8 mmol, 1.1 equiv) was added and the mixture allowed to stir overnight (17 h).
At this point, the mixture was placed under low vacuum (~10 min) and back filled with dry argon. To this was added 377 mg of 10% Pd/C (dry), the atmosphere removed under vacuum and converted to one of hydrogen. The reduction was followed via HPLC, where after consumption of the starting material, the Pd was removed by filtration under a blanket of argon. The filtrate was evaporated to dryness and the residue purified via HPLC (5-85%
0.1 % TFA CH3CN / 0.1 % TFA water). The desired fractions were combined and the CH3CN removed in vacuo. The remaining aqueous solution was then basified with saturated NaHC03 and extracted with EtOAc (1 x 350 mL). The organic was separated, rinsed with water (100 mL) and then brine (100 mL), dried over Na~S04, filtered, and evaporated. To the red solid was added 75 mL of hot water and the solids sonicated and then filtered to provide 2.77 g (66%) of the desired product as a red solid.
~H-NMR
(DMSO-d6) s 12.43 (br s, 1 H), 10.79 (br s, 1 H), 7.94 (s, 1 H), 7.73 (d, 1 H), 7.46 (d, 1 H), 7.33-7.28 (m, 1 H), 7.26-7.18 (m, 3H), 7.10 (br s, 1 H); LCMS RT = 2.11 min;
[M+H] _ 392.2; EA Calcd C 64.44; H 5.41; N 17.89, Found C 64.18, H 5.19, N 17.70.

Example 104 Preparation of 3-acetylamino-2-(3-oxo-3.4-dihydro-puinoxalin-2-yl)-1H-indole-5-carboxylic acid 2-methox rL-ethyl)-methy!-amide O
H3C~0 N
HN. CH3 N
H
H
O
In a 50 mL round bottom flask was placed 52.0 mg (0.13 mmol, 1 equiv) of 3-amino-2-(3-oxo-3,4-dihydro-quinoxalin-2-yl)-1 H indole-5-carboxylic acid (2-methoxy-ethyl)methylamide (Example 56) in 5 mL of THF. To this was added 12.6 mg (0.16 mmol, 0.013 ml, 1.2 equiv) of pyridine and 11.5 mg (0.15 mmol, 0.010 mL, 1.1 equiv) of acetyl chloride. This was allowed to stir at room temperature for 72 h. The mixture was then diluted with 40 mL of water and 50 mL of brine and transferred to a separatory funnel.
This mixture was then extracted with EtOAc (3 x 75 mL). The combined organics were dried (Na~S04), filtered, and evaporated to provide 45 mg (78%) of the pure desired product as an orange solid. 'H-NMR (DMSO-d6) ~ 12,82 (s, 1 H), 11.72 (s, 1 H), 10.73 (s, 1 H), 7.93 (s, 1 H), 7.87 (d, 1 H), 7.62 (d, 1 H), 7.53 (dt, 1 H), 7.37 (dt, 2H), 7.23 (d, 1 H), 3.70-3.11 (br m, 7H), 3.01 (s, 3H), 2.22 (s, 3H); LCMS RT = 2.63 min; [M+H] =
434.14.
Example 134 Preparation of 3-amino-2-(6,7-dichloro-3-oxo-3,4-dihvdro-2-quinoxalinY~-N f2-(diethylamino)ethyfl-N-meth~rl-1 H-indole-5-carboxamide Hs N
N

CI
CI

In a 25 mL flask was placed 2-(6,7-dichloro-3-oxo-3,4-dihydro-2-quinoxalinyl)-vitro-1H indole-5-carboxylic acid (0.100 g, 0.239 mmol), DMF (5 mL), and Et3N
(0.037 mL, 0.262 mmol). To this solution was added PyBOP (0.137 g, 0.262 mmol) and then N
[2-(diethylamino)ethyl]-N methyfamine (0.034 g, 0.262 mmol). The mixture was allowed to stir at rt overnight. SnClz (0.226 g, 1.913 mmol) was added and the mixture was stirred at 80 °C for 4h. The mixture was filtered and concentrated. The residue was taken up in 30 mL of water and extracted with EtOAc (3 x 20 mL). The organics were concentrated and the residue was purified by preparative HPLC (CH3CN/H~O
0.1°l° TFA). 'H NMR
(400 MHz, DMSO) b 12.49 (s, 1 H), 10.71 (s, 1 H), 8.10 (s, 1 H), 7.98 (s, 1 H), 7.44 (d, J =
8.8 Hz, 2H), 7.34 (s, 1 H), 7.30 (s, 1 H), 7.21 (d, J = 9.6 Hz, 2H), 3.44 (bs, 2H), 2.99 (s, 3H), 2.33 (bs, 2H), 0.93 (br d, 6H); LCMS RT = 2.47 min; [M+H]=501.1.
Examale 151 Preparation of N (,~3R~1~'[3-amino-2-(3-oxo-3,4-dihydroauinoxalin-2-yl)-1H
indol-5-girl]carbonyl~eyrrolidin-3-y~acetamide N~
'NH
O-' 'CH3 N O
H
Step 1. Preparation of 3-(5-~[~3R)-3-aminopyrrolidin-1-yllcarbonyl)-3-vitro-1H
indol-2-yl)auinoxalin-2(1 H -one H
O
N~
'NH
O~N -N~ N~
H
N O
To a solution of ferf-butyl ((3R)-1-{[3-vitro-2-(3-oxo-3,4-dihydroquinoxalin-2-yl)-1H-indol-5-yl]carbonyl}pyrrolidin-3-yl)carbamate (Prepared using the experimental method described to produce Example 56, 0.40 g, 0.77 mmol) in CH2Ch (5 mL was added TFA (1 mL). The resulting red solution was stirred at rt for 3 h before the volatiles were removed and EtzO was added. The volatiles were removed to provide a yellow crude residue. To this residue was added Et~O and the mixture was sonicated. The precipitated yellow solid was filtered and washed with Et20 before being dried in an oven to provide 360 mg of a yellow solid (88%). This material was used in next step reaction without purification.
Step 2. Preparation of N ((3R)-1-~f3-vitro-2- 3-oxo-3 4-dih r~droquinoxalin-2-yl)-1H-indol-5 yllcarbonyl~pyrrolidin-3-yl)acetamide O
N~
" 'NH

O~CHs N~ H~
N O
H
In a 50 mL rb flask was placed 3-(5-{[(3R)-3-aminopyrrolidin-1-yl]carbonyl)-3-vitro-1H-indol-2-yl)quinoxalin-2(1H)-one (0.10 g, 0.19 mmol) in DMF (5 mL). To this solution was added AcCI (0.015 g, 0.19 mmol) and the mixture was allowed to stir for 3 h at rt. Pd/C was added and the atmosphere was converted to HZ before the reaction was stirred for 3 h. The resulting red solution was filtered and concentrated providing a residue that was purified via HPLC (CH3CN/water = 15-80%) to yield 14.6 mg of a red solid (18%). ~H-NMR (DMSO-d6) ~ 12.44 (s, 1 H), 10.82 (s, 1 H), 8.17 (s, 1 H), 8.06 (s, 1 H), 7.75-7.71 (d, 1 H), 7.47-7.43 (d, 1 H), 7.39-7.35 (d, 1 H), 7.32-7.28 (m, 1 H), 7.25-7.21 (m, 2H), 7.13 (s, 2H), 4.13 (s, 1 H), 3.80 (s, 1 H), 3.70-3.49 (m, 3H), 2.11-2.01 (m, 1 H), 1.85-1.74 (m, 4H). LCMS RT = 1.97 min; [M+H]+ = 431Ø
Example 152 Preparation of tent-butyl 5-(4-cyanophen rl -1H indole-1-carboxylate CN
N
H3C3~O~O

Step 1. Preparation of 4-(1H indol-5- rLl)benzonitrile N
H
Na was bubbled through a solution of 5-indolylboronic acid (1.50 g, 9.32 mmol) in DME (55 mL) for 10 min. To this solution was added 1,1'-bis-(diphenylphosphine-ferrocene) dichloropalladium (II) complex with CH2CI2 (1:1) (0.382 g, 0.440 mmol), 1.OM
solution of Na2C03 (22 ml, 22 mmol) and 4-bromobenzonitrile (1.60 g, 8.87 mmol). N2 Was then bubbled through the reaction mixture for 10 min before the mixture was heated at 60 °C for 1 h. The reaction was quenched with H20 and extracted with EtOAc (3x). The combined organic layers were washed with H20, brine, dried (MgS04), and concentrated to provide 2.24 g of crude brownish solid residue which was used in next step reaction without purification.'H-NMR (DMSO-d6) 8 11.24 (s 1H), 7.91 (s, 1H), 7.85 (s, 4H), 7.47-7.45 (m, 2H), 7.39 (d, 1 H), 6.49 (d, 1 H).
Step 2. Preparation of tert-buty~4-cyan~henyl)-1H indole-1-carbox I

HsC~O

In a 100 mL rb flask was placed 4-(1H indol-5-yl)benzonitrile (2.24 g, 10.3 mmol) in 100 mL of anhydrous THF. To this solution was added DMAP (0.630 g, 5.13 mmol) and the mixture allowed to stir for 0.5 h at rt. Boc20 (2.24 g, 10.3 mmol) was added and the reaction stirred for 2 h. The reaction was then quenched with H2O and extracted with Et20 (2x). The combined organic layers were washed with 1 N HCI, H2O (2x), brine, dried (MgS04), and concentrated to provide 2.20 g (67°l°) of an off white solid. 'H-NMR
(DMSO-d6) s 8.13-8.11 (d, 1 H), 8.00 (s, 1 H), 7.90 (s, 4H), 7.72-7.68 (m, 2H), 6.77 (d, 1 H), 1.63 (s, 9H).

Example 155 Preparation of 3-f3-amino-5-[4-phenylpiperidin-1-yl)carbonyll-1H-indol-2-yl)auinoxalin-2 1 H -one ~N -\ /

\ ~yN
H
N O
H
To a solution of SOCK (20.0 mL, 272 mmol) was added 3-nitro-2-(3-oxo-3,4-dihydroquinoxalin-2-yl)-1H-indole-5-carboxylic acid (Example 22, 250 mg, 0.710 mmol) at rt and the resulting brown suspension was heated at 85 °C for 4 h. The suspension was concentrated under reduced pressure and the residue dried for 24 h in vacuo to give 262 mg of light yellow solid. The crude acid chloride was used without further purification. The solid was suspended in anhydrous CH2CI2 (30 mL) and 4-phenylpiperidine (128 mg, 0.780 mmol) was added at rt followed by Et3N (0.110 mL, 0.780 mmol). The reaction becomes a clear solution after a few minutes and it was stirred at rt for 24 h. To the solution was added 10% Pd/C (50 mg) and the reaction hydrogenated at 1 atm and rt for 2 h. The reaction was diluted with DMF (100 mL) to dissolve the red precipitate (product) then quenched by addition of sat. NH4CI (200 mL). The mixture was extracted with EtOAc (2 X 200 mL) and the organics dried (Na2S04). The solution was filtered and concentrated in vacuo to give a red residue. The crude product was dissolved in DMF and purified by reverse-phase prep-HPLC. Desired fractions were diluted in EtOAc (150 mL) and washed with sat. NaHC03 (100 mL). The organics were dried (NaZS04), filtered, and concentrated in vacuo to give a red solid. This was suspended in CH2CI2 and hexane, sonicated, and filtered washing with hexane to give the product as a brick red solid powder in 9% yield (30 mg, 0.065 mmol) after drying. TLC: Rf = 0.40 (66% EtOAc/hexane; LC-MS
(ESI):
[M+H]+ = 464.2 a~ RT = 2.87 min.; ~H NMR (DMSO-d6) & 12.43 (1 H, s), 10.81 (1 H, s), 7.98 (1 H, s), 7.73 (1 H, d, J = 9.2 Hz), 7.48 (1 H, d, J = 8.8 Hz), 7.15 -7.35 (9H, m), 4.25 (2H, v bs), 3.00 (2H, bs), 2.83 (1 H, m), 1.80 (2H, m), 1.64 (2H, m).

Example 156 Preparation of 3-f3-amino-5-(moraholin-4-ylmethyl)-1H indol-2-~rllquinoxalin-2(1H-one N O
U

W Nw H
a N O
H
Stea 1. Preparation of 3-~3-amino-5-(hydroxymethLrl)-1H indol-2-Yllquinoxalin-2~1H -one OH
O~N -I \ N\ H/
N O
H
To a solution of 3-nitro-2-(3-oxo-3,4-dihydroquinoxalin-2-yl)-1 H-indole-5-carboxylic acid (Example 22, 4.36 g, 12.3 mmol) in anhydrous DMF (500 mL) at rt was added CDI
(3.03 g, 18.5 mmol) and the dark amber solution stirred at rt for 48 h. The reaction was concentrated under reduced pressure at 30 °C to a volume of 200 mL, then diluted with anhydrous THF (100 mL). The reaction was cooled to 0 °C in an ice bath and vigorously stirred as a rt solution of NaBHa (980 mg, 24.64 mmol) in H2O (100 ml) was added. The reaction, which evolves gas for the first minute, was stirred at 0 °C
for 40 min, then quenched with cone. HCI (50 mL) added over 2 min. The mixture was stirred in the ice bath for 5 min, then added portionwise to a stirring solution of sat. NaHC03 (1 L) at rt over min. This was extracted with EtOAc (3 X 1 L). A yellow precipitate was filtered from the biphase and washed with water then EtOAc. The organics were dried (Na2S04), then filtered and concentrated to a volume of approx. 50 mL (DMF). This was diluted with 1:1 MeOHIEtOAc (300 mL), sonicated for 30 min, then let sit for 24 h. The yellow precipitate was filtered washing with EtOAc then hexane. The two precipitates were combined and dried in vacuo under P205 to give the product as a yellow solid in 64% yield (2.74 g, 8.16 mmol). TLC: Rf = 0.69 (EtOAc); LC-MS (ESI): [M+H]~ = 337.0 @ RT= 2.13 min.; 'H
NMR (DMSO-d6) 8 12.80 (2H, v bs), 8.04 (1 H, s), 7.85 (1 H, d, J = 8.0 Hz), 7.63 (1 H, m), 7.52 (1 H, d, J = 8.4 Hz), 7.38 (2H, m), 7.29 (1 H, d, J = 7.2 Hz), 5.29 (1 H, t, J = 5.6 Hz), 4.64 (2H, d, J = 5.2 Hz).

Step 2. Preparation of 3-f3-vitro-5~bromomethyl)-1H-indol-2-yllauinoxalin-2(1Hl-one H
To a solution of 3-[3-vitro-5-(hydroxymethyl)-1H-indol-2-yf]quinoxalin-2(1H)-one (3.04 g, 8.94 mmol) in anhydrous DMF (15.0 mL, 195 mmol) was added anhydrous CH~CI2 (30 mL), followed by SOBr2 (17.5 mL, 223 mmol) at ambient temp. over 1 min.
The reaction becomes hot and bubbles vigorously for several minutes. The mixture was stirred at ambient temp. for 1 h during which time the reaction becomes a dark gray solution. The reaction was poured into CH2Ch (1.5 L) and carefully quenched with sat.
NaHC03 (1.7 L). The reaction temp. was kept below 25 °C and the final pH is 7.5. The yellow precipitate which forms in the biphase aqueous layer during the quench was filtered off, washed with HBO (3 X 50 mL). The aqueous was extracted with CH2CI2 (1 L), and the combined organics dried (Na2S04), filtered, and concentrated in vacuo to a yellow semi-suspension in the remaining DMF (5 mL). This was diluted with CH2Ch (10 mL) and copious amounts of hexane was added (200 mL) to give a yellow precipitate. The solid was filtered, washed with hexane, added to the precipitate obtained above, and the combined solids dried in vacuo under P205 to give the product as a yellow solid (2.81 g, 75%). The crude bromide was used without further purification. TLC: Rf = 0.35 (66%
EtOAc/hexane); LC-MS (ESI): [M+H]+ = 398.9/400.8 @ RT= 2.85 min.
Steep 3 Preparation 3~~moraholin-4-methyl)-3-vitro-1 H indol-2-yllauinoxalin-2(1 M-one 1~1 N O
U
To a solution of the crude 3-[3-amino-5-(bromomethyl)-1H indol-2-yl]quinoxalin-2(1H)-one (100 mg, 0.250 mmol) in anhydrous DMF (1.5 mL) at rt was added morpholine (1.00 mL, 11.5 mmol) and the amber solution stirred at rt for 5 h. The reaction was quenched with sat. NH4CI (200 mL) and extracted with EtOAc (3 X 250 mL). The combined organics were dried (Na~S04), filtered, then concentrated in vacuo to give a yellow oil. This was purified by silica gel chromatography (10% MeOH/EtOAc) to give the product as a yellow solid in 99% yield (105 mg, 0.250 mmol). TLC: Rf = 0.33 (5%
MeOH/EtOAc); LC-MS (ESI): [M+H]+ = 406.0 @ RT= 1.73 min.; 'H NMR (DMSO-ds) 8 13.11 (1 H, bs), 12.82 (1 H, bs), 8.02 (1 H, s), 7.87 (1 H, d, J = 8.0 Hz), 7.65 (1 H, t, J = 7.2 Hz), 7.56 (1H, d, J = 8.4 Hz), 7.38 (3H, m), 3.62 (2H, s), 3.57 (4H, m), 2.34 (4H, m).
Step 4. Preparation of 3-f3-amino-5-(morpholin-4-ylmeth rLI)-1H indol-2-y]auinoxalin-2 1H -one N O
~J
HZN
~ ~ ~~N
H
N O
H
To a solution of 3-[5-(morpholin-4-ylmethyl)-3-nitro-1H indol-2-yl]quinoxalin-2(1H)-one (100 mg, 0.240 mmol) in anhydrous DMF (5 mL) at rt was added 10% Pd/C (10 mg).
The reaction was hydrogenated at 1 atm for 1 h. The mixture was purified directly by silica gel chromatography (10% MeOH/EtOAc) to give the product as a brick red solid in 28% yield (78 mg, 0.21 mmol). TLC: Rf = 0.55 (EtOAc); LC-MS (ESI): [M+H]+ =
375.8@
RT= 1.51 min.; ~H NMR (DMSO-ds) 8 12.38 (1 H, s), 10.53 (1 H, s), 7.70 (2H, m), 7.37 (1H, d, J = 8.4 Hz), 7.28 (1H, m), 7.22 (2H, m), 7.11 (1H, d, J = 8.4 Hz), 7.01 (2H, s), 3.56 (4H, m), 3.47 (2H, s), 2.35 (4H, bs).
Example 158 Preparation of 1-(methylsulfonyl)piperazine O ~ .CH3 CND
N
H
Step 1. Preparation of tert butyl 4- methylsulfonyl)piperazine-1-carboxylate O ~ .CH3 cN~
N
O~O
H3C_ CHCH3 To a solution of tert-butyl piperazine-1-carboxylate (0.60 g, 3.2 mmol) in (10 mL) was added Et3N (0.65 g, 6.4 mmol). The mixture was stirred for 10 min before methanesulfonyf chloride (0.40 g, 3.5 mmol) was added and the mixture allowed to stir overnight at rt. The reaction was quenched with H20 and extracted with CH~CIa (2x). The combined organic layers were washed with H20, brine, dried (MgS04), filtered and concentrated to provide 0.80 g of an off-white solid (93%). ~H-NMR (DMSO-d6) 8 3.41-3.38 (t, 4H), 3.08-3.04 (t, 4H), 2.85 (s, 3H), 1.40 (s, 9H).
Step 2. Preparation of 1-(methylsulfonyl~piperazine O ~ .CH3 CND
N
H
To a solution of tert-butyl 4-(methylsulfonyl)piperazine-1-carboxylate (0.80 g, 3.0 mmol) in CHZCI2 (10 mL} was added TFA (1 mL). The mixture was stirred at rt for 3 h before the volatiles were removed. Et20 was added to the residue then removed in vacuo to provide a yellow residue. Et20 was added and the mixture was sonicated. The white solid precipitate was filtered, washed with Et20, and dried in an oven to provide 530 mg of an off-white solid (64%).'H-NMR (DMSO-ds) 8 9.06 (s, 2H), 3.34-3.31 (m, 4H), 3.21-3.18 (m, 4H), 2.98 (s, 3H). LCMS [M+H]+ = 165.1.
Example 160 Preparation of 3-(3-amino-5-f(2-methoxyethoxy; methyll-1 H-indol-2-yl~
uinoxalin-2(1 H)-one O O

H2N~
~ ~yH
N O
To a suspension of the crude 3-[3-amino-5-(bromomethyl)-1H-indol-2-yl]quinoxalin-2(1H)-one (see steps 1-2, example 156; 1.50 g, 3.76 mmol) in 2-methoxyethanol (29.4 mL, 372 mmol) at rt was added the minimal amount of anhydrous DMF to give a clear solution (35 mL). To this was added K2C03 powder (1.56 g, 11.3 mmol) and additional DMF (10 mL). The mixture was stirred at rt for 18 h. The reaction was filtered to remove K2C03 and concentrated to an oily residue. This was redissolved in DMF (5 mL) and refiltered to remove more K2C03 solids. The solvent was again removed in vacuo and the gum dried in vacuo for 3 h to remove all solvents. The ether-coupled intermediate was dissolved in anhydrous DMF (60 mL) and 10% Pd/C added (3.0 g). This was hydrogenated at 1 atm for 45 min. The red reaction solution was filtered to remove Pd/C, washing with MeOH (200 mL), then concentrated to a volume of 50 mL
(DMF). This was refiltered to remove traces of Pd/C and more precipitated K2C03. The filtrate was concentrated further to a volume of 30 mL DMF and purified by reverse-phase prep-HPLC. Desired fractions were diluted in EtOAc (1 L) and washed with sat.
NaHC03 (500 mL). The organic layer was dried (Na2S04), filtered, and concentrated in vacuo to give a red solid. This was suspended in CH2CI2 (150 mL) and diluted with hexane (200 mL). The brick-red solid was filtered, washed with hexane, and dried in vacuo under P205 to give the product in 29% yield (400 mg, 1.10 mmol). TLC: Rf = 0.70 (EtOAc); LC-MS
(ESI):
[M+H]+ = 365.1 @ RT= 2.14 min.; 'H NMR (DMSO-ds) 8 12.40 (1 H, s), 10.60 (1 H, s), 7.73 (2H, m), 7.41 (1H, d, J = 8.4 Hz), 7.29 (1H, m), 7.24 (2H, m), 7.13 (1H, dd, J = 1.2, 8.4 Hz), 7.04 (2H, s), 4.49 (2H, s), 3.55 (2H, m), 3.49 (2H, m), 3.25 (3H, s).
Example 196 Preparation of 3-amino-N f(4-methoxyphenyl)sulfonyll-2-(3-oxo-3 4-dihydroauinoxalin-2 yl)-1 H-indole-5-carboxamide S ~ / OMe N
H
IV lJ
H
To a 25 mL rb flask was added 3-nitro-2-(3-oxo-3,4-dihydroquinoxalin-2-yl)-1 H-indole-5-carboxylic acid (Example 22, 0.100 g, 0.285 mmol), DMF (5 mL), 4-methoxybenzenesulfonamide (0.059 g, 0.314 mmol), DMAP (0.038 g, 0.314 mmol) followed by EDCI (0.060 g, 0.314 mmol). The reaction mixture was allowed to stir at ambient temperature for 4 h before the flask was purged with argon. Pd/C
(0.250 g) was added to the flask and a balloon was fitted with hydrogen and the flask was purged (3x).
The hydrogenation was allowed to stir at rt for 12 h. The reaction mixture was then filtered and purified by HPLC. The desired fractions were then combined, sat.
NaHC03 was added (5 mL), and the mixture was extracted with EtOAc (3 x 50 mL). The combined organics were dried over Na2S04 and then concentrated to provide a red solid.
'H NMR
(400 MHz, DMSO) 8 12.43 (s, 1 H), 10.90 (s, 1 H) 8.5 (s, 1 H), 7.93 (d, J =
8.8 Hz, 2H), 7.70 (d, J = 8.8 Hz) , 7.45 (d, J = 9.2), 7.35 (m, 3H), 7.29 (m, 3H),7.25 (bs, 2H), 7.09 (d, J = 8.4), 3.85 (s, 3H). LCMS RT = 2.77 min; [M+H]+ = 490.1.
Example 214 Preoaration of N-(1-ff3-amino-2-(3-oxo-3,4-dihydroauinoxalin-2-yl)-1H-indol-5-yllcarbonyl;pyrrolidin-3-yl)-N'-isopropyl-N methylurea O
N
N.CH3 HzN -I \ / O~NH
\ N\ N~
H HsC~CHs N O
H
Step 1 Pre~aaration of 3-(5-ff3- methylaminoLyrrolidin-1-yllcarbonyl~-3-nitro-1H-indol-2-Lrl)g uinoxalin-2(1 H)-one N,CH3 H
IV V
H
To a solution of tert-butyl methyl(1-{[3-nitro-2-(3-oxo-3,4-dihydroquinoxalin-2-yl)-1 H indol-5-yl]carbonyl}pyrrolidin-3-yl)carbamate (Prepared using the experimental method described to produce Example 56, 0.70 g, 0.77 mmol) in CH2CI2 (10 mL) was added TFA (10 mL), and the resulting red solution was stirred at rt overnight.
The volatiles were evaporated and ethyl ether was added. The volatiles were evaporated again to provide a crude yellow residue. This residue was basified with saturated NaHC03 to pH 9. The precipitated yellow solid was filtered, washed with water, and dried in an oven to provide 471 mg of a yellow solid (83%). This material was used without further purification.
Step 2 Preparation of N (1~f3-amino-2-(3-oxo-3 4-dihydroquinoxalin-2-yl)-1H-indol-5-yllcarbonyl~pyrrolidin-3- rLI~N'-isopropyl-N methylurea N
N.CH3 HEN - f N I ~ ~ O~NH
w H.
HsC~CH3 N O
H

In a 25 mL rb flask was placed 3-(5-{[3-(methylamino)pyrrolidin-1-yl]carbonyl}-nitro-1H indol-2-yl)quinoxalin-2(1H)-one (0.10 g, 0.23 mmol) in toluene (10 mL). To this suspension was added isopropyl isocyanate (0.020g, 0.23 mmol) and the mixture was allowed to stir overnight at reflux. The solvent was evaporated and to the residue was added ether followed by sonication. The precipitated solid was filtered, washed with ether, and dried in an oven to provide desired a yellow solid. This crude yellow solid was dissolved in DMF (5 mL) and to this solution was added Pd/C. The atmosphere was converted to hydrogen and the reaction was stirred for 3h. The resulting red solution was filtered and the Pd residue was washed with DMF. The red solution was concentrated and residue was purified via HPLC (MeCNlwater = 15-80%). The fractions were combined and evaporated to remove acetonitrile. The red solution was basified (saturated NaHC03) and the red precipitate was filtered, washed with water (5x), and dried in the oven to provide 66 mg of a red solid (59%). 'H-NMR (DMSO-d6) 8 12.43 (s, 1H), 10.81 (s, 1 H), 8.12 (s, 1 H), 7.76-7.73 (d, 1 H), 7.49-7.43 (d, 1 H), 7.40-7.35 (m, 1 H), 7.33-7.29 (m, 1 H), 7.28-7.21 (m, 2H), 7.15 (s, 2H), 6.02 (s, 1 H), 3.81-3.39 (m, 5H), 2.73 (s, 3H), 1.99-1.87 (m, 2H), 1.09-0.95 (m, 6H). LCMS RT = 2.17 min; [M+H]~ = 488.1.
Example 217 Preparation of 3-~3-amino-5-(3 5-dichloro-pyridin-4-yloxY)-1H-indol-2-yll-1H-auinoxalin-2-one CI
w o ~ ~N
H2N ~ CI
N
H
N~ ~'O
H
Step 1 Preparation of 3-(5-Hydroxy-1H-indol-2-yl)-1H-auinoxalin-2-one H
H
A solution of 3-(5-methoxy-1 H-indol-2-y1)-1 H-quinoxalin-2-one (Example 6, 1.80 g, 6.18 mmol) in CHZCI2 (150 mL) was cooled to 0 °C. BBr3 (5.84 mL, 61.8 mmol) was added to the solution dropwise. The mixture was stirred at rt for 24 h. The reaction was poured onto ice (200 g). The resulting mixture was extracted with EtOAc (3 X
300 mL).

The organic layers were washed with brine (500 mL), dried (MgS04) and concentrated under reduced pressure. The residue was crystallized in MeOH and water (1:6) to afford 1.70 g (99%) of product. 1 H NMR (400 MHz, DMSO) 8 12.56 (s, 1 H), 11.31 (s, 1 H), 8.79 (s, 1 H), 7.78 (d, J = 8.4 Hz, 1 H), 7.64 (s, 1 H), 7.46 (t, J = 7.2 Hz, 1 H), 7.30-7.32 (m, 3H), 6.90 (s, 1 H), 6.73 (d J =8.4 Hz, 1 H); LCMS (ESI-MS) RT = 2.27; 276.2 (M+H)+.
Step 2 Preparation of 3 j5-(3 5-Dichloro-p ridin-4-yloxyl-1 H-indol-2-yll-1 H-auinoxalin-2-one ca H
A solution of 3-(5-hydroxy-1 H-indol-2-yl)-1 H-quinoxalin-2-one (100 mg, 0.36 mmol) and potassium terf-butoxide (44.5 mg, 0.40 mmol) in DMF (2 mL) was stirred at rt for 2 h. To the solution, was added 3, 4, 5-trichloropyridine (65.8 mg, 0.36 mmol) and 1~2CO3 (29.9 mg, 0.22 mmol). The mixture was heated to 100 °C
overnight. The reaction was allowed to cool to rt and poured into water (20 mL). The crude product was precipitated as a yellow solid. The solid was filtered, washed with water and dried to give 120 mg (79%) of product. 1 H NMR (400 MHz, DMSO) 8 12.60 (b, 1 H), 11.69 (s, 1 H), 8.75 (s, 2H), 7.81 (d, J = 8.8 Hz, 1 H), 7.73 (s, 1 H), 7.51 (m, 2H), 7.34-7.32 (m, 2H), 7.05 (s, 1 H), 6.95 (d J =8.8 Hz, 1 H); LCMS (ESI-MS) ~RT = 3.77; 423.2 (M+H)+.
Step 3 Preparation of 3-f5-(3 5-dichloro-pryrindine-4-yloxy)-3-nitro-1H indol-2-yll-1H
auinoxalin-2-one CI
w O ~ ~N
02N ~ CI
N O
H
To a solution of 3-[5-(3,5-dichloro-pyridin-4-yloxy)-1H-indol-2-yl]-1H-quinoxalin-2-one (110 mg, 0.26 mmol) in DMF (3 mL) was added isoamyl nitrite (80 uL, 0.57 mmol).
The reaction was heated at 90 °C for 2 h, then allowed to coot to rt.
The mixture was poured into water (25 mL). The product was precipitated as a yellow solid. The solid was filtered, washed with water and dried to afford 95 mg (62%) of crude product which was used without further purification.
Step 4 Preparation of 3-[3-Amino-5-(3 5-dichloro-pyridin-4-yloxy)-1H-indol-2-yll-1H
g_uinoxalin-2-one CI
O ~ ~N
HEN ~ / CI
i N~ H
a~
N O
H
A solution of 3-[5-(3,5-dichloro-pryrindine-4-yloxy)-3-vitro-1 H-indol-2-yl]-1 H-quinoxalin-2-one (95 mg, 0.16 mmol) in AcOH (2 mL) and water (20 uL) was degassed with nitrogen for 5 min. Activated iron powder (325 mesh, 95 mg, 1.70 mmol) was added and the mixture was stirred at rt overnight. The reaction was neutralized by NaHC03 solution (50 mL) and extracted with EtOAc (3 X 30 mL). The organic layers were washed with brine (50 mL), dried and concentrated. The residue was purified by a silica gel column chromatography (EtOAc : Hexanes = 1 :1 ) to afford 35 mg (49%) of desired product. 1 H NMR (400 MHz, DMSO) b 12.45 (s, 1 H), 10.66 (s, 1 H), 8.78 (s, 2H), 7.73 (d, J = 8.8 Hz, 1 H), 7.48 (d, J = 8.8 Hz, 1 H), 7.24-7.00 (m, 5H), 6.85 (s, 2H);
LCMS (ESI-MS) RT = 2.99; 438.2 (M+H)+.
Example 228 Preparation of 3-(~~~[tert-butyl(dimeth~ silylloxY~-1H-indol-2-yl)auinoxalin-2(1H)-one DMS
H
Step 1 Preparation of 5-f tent-butyl~dimeth~)silylloxy~-1 H-indole OTBDMS
N
H
In a 250 mL rb flask was placed 5-hydroxyindole (5.00 g, 37.6 mmol, 1 equiv.) in 75 mL of DMF. To this was added imidazole (2.7 g, 1.05 equiv.) and TBDMSCI
(5.90 g, 1.05 equiv.) and the reaction was allowed to stir at room temperature for 2 h.
The DMF

was removed in vacuo and the residue was partitioned between water (150 mL) and EtOAc (150 mL). The EtOAc was removed and the aqueous extracted (2 x 100 mL) with EtOAc. The combined organics were dried (Na2S04), filtered, and evaporated to provide 9.2 g of a white solid which was used without further purification.
Stea 2. Preparation of tert-butyl 5-(ftert-butyl(dimeth r~l silylloxy~-1 H-indole-1 carbox late OTBDMS
N
O~O
~CH3 HsC CHs In a 250 mL rb flask was placed 9.3 g (37.6 mmol, 1 equiv) of 5-t-butyldimethylsiloxyindole in 75 mL of THF. To this was added 4-DMAP (4.8 g, 1.05 equiv) and di-t butyl dicarbonate (8.6 g, 1.05 equiv) after which gas evolution was evident. After gas evolution ceased (5 min.) the reaction appeared complete via TLC.
The THF was then removed and the residue partitioned between water (150 mL) and EtOAc (150 mL). The organics were separated, dried (Na2S04), filtered, and evaporated.
The residue was then filtered through a silica plug to remove any remaining 4-DMAP.
The desired fractions were combined and evaporated to provide 12.2 g of a white solid which was used without further purification.
Step 3. Preparation of tert-butyl 5-fftert-but~i~dimeth I)silylloxy~[methox~oxo acet r~l' 1H indole-1-carboxylate OTBDMS
O
MeO
O O
O
H3C- 'CH Hs In a 500 mL rb flask was placed N Boc-5-t-butyldimethylsiloxyindole (12.2 g, 35.1 mmol, 1 equiv) in 100 mL of THF. This was cooled to -78 °C where 24.1 mL of t-BuLi (1.7 M in pentane, 38.6 mmol, 1.1 equiv) was added dropwise. This was allowed to stir for 1h, where dimethyl oxalate (9.1 g, 2.2 equiv) was added as a solution in 40 mL of THF
quickly in one portion. The reaction was then allowed to warm to room temp.
and stir for an additional 2 h. At this point, the reaction was diluted with water (200 mL) and extracted with EtOAc (3 x 150 mL). The combined organics were dried (Na2S04), filtered, and evaporated. The residue was then purified by silica gel chromatography (10%EtOAc/Hex) to provide 8.9 g (58%) as a white solid. ~H NMR (CD2CI2) 8 7.72 (d, 1 H), 7.34 (d, 1 H), 6.77 (s, 1 H), 6.61 (d, 1 H), 6.25 (d, 1 H), 1.44 (s, 9H), 0.80 (s, 9H), 0.00 (s, 6H); TLC Rf = 0.60 (25%EtOAc/Hex).
Step 4 Preparation of 3-(5-~ftert but rLl(dimethLrl silylloxy)-1H indol-2-yl)auinoxalin-2(1H)-one In a 500 mL rb flask was placed N Boc-5-t-butyldimethylsiloxy-2-methyloxalylindole (8.70 g, 20.0 mmol, 1 equiv) in 250 mL of AcOH. To this was added 1,2-phenylenediamine (2.4 g, 1.1 equiv) and the reaction mixture heated at 130 °C. After 1h, 1.7 mL of TFA (1.1 equiv) was added turning the solution red. After 2 min, the reaction was cooled to room temp. and poured into 60 mL of water resulting in a yellow solid. The solid was filtered and dried in vacuo at 60 °C to provide 7.8 g (99%) of the desired product as a yellow solid. 'H NMR (DMSO-d6) 8 12.39 (s, 1H), 11.26 (s, 1H), 7.61 (d, 1 H), 7.52 (s, 1 H), 7.30 (dt, 1 H), 7.20 (d, 1 H), 7.14 (m, 2H), 6.85 (d, 1 H), 6.57 (dd, 1 H), 0.78 (s, 9H), 0.00 (s, 6H); LCMS RT = 3.98 min; [M+H]=392.3.
Example 236 Preparation of 3-f3-amino-5-(2 3-dihydro-1H-tetrazol-5-yl)-1H-indol 2-yllauinoxalin-211H -one .N.N
i NH

Step 1. Preparation of 3-f5-(2.3-dihydro-1H-tetrazol-5-yl)-3-nitro-1H-indol-2-~Lg~uinoxalin-2 1 H -one N~N
NH
In a 25 ml rb flask was placed 3-[3-nitro-5-cyano-1 H-indol-2-yl]-1 H-quinoxalin-2-one (Example 19, 150 mg, 0.45 mmol) in 5 ml of DMF. To this was added NaN3 (58.9 mg, 0.90 mmol) and NH4CI (48.4 mg, 0.90mmol) before the reaction was heated at °G. After 1 h, only minor product was seen and 1 ml of water was added.
Stirring another 1 h produced only a minor change. Additional NaN3 (176 mg) and NH4CI (145 mg) were added and the reaction was allowed to stir over the weekend. At this point, no starting material remained. The solids were filtered off and the majority of volatiles (~2 ml) removed. The mixture was then diluted with water and filtered to provide 117 mg (69%) of yellow solid that was used without further purification. LCMS Rt=2.22 min;
[M+H]=375Ø
Step 2. Preparation of 3 ~3-amino-5-(2,3-dihydro-1 H-tetrazol-5-yl -1 H-indol-2-yllauinoxalin-2(1H -one ,N.N
N
NH

N\ H~
N O
H
In a 25 ml rb flask was placed 3-[3-nitro-5-(1H tetrazol-5-yl)-1H indol-2-yl]-quinoxalin-2-one (117 mg, 0.31 mmol) in 6 ml of DMF. To this was added catalytic 10%
PdJC and the dissolved gases removed under vacuum. The atmosphere was converted to one of Hz and the reaction was allowed to stir at rt until complete. The Pd/C was then filtered off and the volatiles removed in vacuo. The solids were suspended in CH3CN, sonicated for 2 minutes, and refiltered to remove any remaining DMF. The desired product was isolated a red solid (84 mg, 82%). 'H-NMR (DMSO-d6; tetrazole N-H

undescribed) b 12.47 (s, 1 H), 10.93 (s, 1 H), 8.59 (s, 1 H), 7.76 (d, 2H), 7.60 (s, 1 H), 7.32 (t, 1 H), 7.25 (t, 2H), 7.19 (br s, 2H). LCMS RT=2.09 min; [M+H]=345Ø
Example 266 Preparation of 3-(3-hydrox rL-1 H indol-2-yl~cluinoxalin-2(1 H -one HO
N~ N~
H
N O
H
Step 1. Preparation of 3-fftert butyl(dimeth~, sil r~l oxy~-1H-indole TBDMSO
\
N
H
To a 100 mL rb flask was added 3-hydroxyindole (1.00 g, 7.51 mmol) followed by TBDMSCI (11.3 mL, 1.OM in THF). Imidazole (0.767 g, 11.3 mmol) was added followed by DBU (0.057 g, 0.38 mmol). The mixture was allowed to stir at rt for 18 h before it was concentrated and used without further purification.
Step 2. Preparation of tert butyl 3-~(tert-butyl(dimethyl silyl]oxy}-1H-indole-1-carboxylate TBDMSO
N
O~O1 /CHs H3C~CH3 To a 100 mL rb flask was added 3-{[tert butyl(dimethyl)silyl]oxy}-1H indole (0.600g, 2.42 mmol) and by 100 mL of THF followed by DMAP (0.311g, 2.55 mmol) and di-tert-butyl di-carbonate (0.556 g, 2.55 mmol). The reaction was allowed to stir at rt for 3 h before it was concentrated and used without further purification.
Step 3. Preparation of terl-butt 3~[tert-buty~dimethyl sily~oxy'~2-[methoxyloxo)acet rL-1 H-indole-1-carboxylate TBDMSO
O
Me0 O O O CHs H3C~CH3 To a 100 mL rb flask was added tert butyl 3-{[tert butyl(dimethyl)silyl)oxy}-indole-1-carboxylate (0.500 g, 1.44 mol) and 100~m1 of THF. The reaction was cooled to -78 °C before t-BuLi (1.7M in pentane, 0.93 mL, 1.6 mmol) was added slowly over 30 min. The solution was then allowed to stir for 2 h at -78 °C before dimethyl oxalate (0.425 g, 3.60 mmol) was added in one portion. The mixture was allowed to stir at -78 °C
for 10 min before it was warmed to 0 °C for 1.5 h. The mixture was quenched with water (100 mL) and concentrated. The residue was purified by column chromatography with Hex/EtOAC (1:1 ) to provide material that was 80% pure. This material was taken on to the next reaction without further purification.
Step 4. Preparation of 3-(3-hydroxy-1H indol-2-yl)auinoxalin-2(1H)-one HO /-N
H
O
To a 100 mL rb flask was added tert butyl 3-{[tert butyl(dimethyl)silyl)oxy}-2-[methoxy(oxo)acetyl)-1 H indole-1-carboxylate (0.030 g , 0.090 mmol) followed by 1,2-phenylenediamine (0.010g, 0.094 mmol) and AcOH (3 mL). The mixture was then heated at 100 °C for 18. The mixture was then concentrated and purified by HPLC. LCMS: RT =
2.94 min., [M+H)+ = 278.7.
Example 304 Preparation of 3-[3-amino-5-(5-methLrl-1,3,4-oxadiazol-2-yl)-1H indol-2-vllquinoxalin-2( 1 H -one N~ iCHs iv a H
To a 30 mL rb flask was added N'-acetyl-3-nitro-2-(3-oxo-3,4-dihydroquinoxalin-yl)-1 H-indole-5-carbohydrazide carbamate (Prepared using the experimental method described to produce Example 56, 0.200g, 0.492 mmol) followed by 5 mL of DMF/Benzene (1l1). P205 (0.284 g, 2.46 mmof) was added and the reaction was heated at 100 °C for 18 h. The mixture was cooled to rt before 10% Pd/C (100 mg) was added and the atmosphere was converted to H2. The mixture was stirred overnight before it was diluted with water (30 mL) and extracted with EtOAc (3x30 mL). The residue was purified by HPLC to provide 0,009 g of a red solid (5%). ~H NMR (DMSQ-d6) b 12.49 (s, 1H), 11.06 (s, 1 H), 8.55 (s, 1 H), 7.70 (m, 1 H), 7.62 (d, 1 H), 7.33 (s, 1 H), 7.25 (m, 1 H), 2.58 (s, 3H); LCMS RT = 2.32 min; [M+H]=359,3.
Example 307 Preparation of 3-amino-N cyclos~entyl-N- 2-methoxyethyl)-2- 3-oxo-3,4-dih~quinoxalin-2-y1~1 H-indole-5-carboxamide O
N

~ N~ H~
a N O
H
Stea 1. Preparation of N (2-methox~et,~ILycloaentylamine ~O.CH3 HN
To a solution of cyclopentanone (2.00 g, 23.8mmol) and 2-methoxyethylamine (1.78 g, 23.8 mmol) in CH2CI2 (10 mL) was added sodium triacetoxyborohydride (7.05 g, 33.3 mmol) followed by AcOH (1.36 mL, 23.8 mmol). The reaction mixture was stirred at rt overnight. The reaction was quenched by adding sat'd NaHC03 and extracted with CHZCI2(2x). The combined organic layers were washed with brine, dried (MgS04), and concentrated to provide 0.70 g (20.5%) of crude free base as an yellowish oil which was used in next step reaction without further purification. 'H-NMR (DMSO-d6) 8 3.37-3.33 (m, 2H), 3.21 (s, 3H), 2.98-2.95 (m, 1 H), 2.63-2.58 (t, 2H), 1.71-1.62 (m, 2H), 1.59-1.52 (m, 2H), 1.43-1.38 (m, 2H), 1.27-1.17 (m, 2H). LCMS RT = 0.76 min; [M+H]+ = 144.2.
Step 2. Preparation of 3-amino-N-cvclopentvl-N l2-methoxvethvl)-2-(3-oxo-3.4-dihydrocluinoxalin-2-YI)-1 H-indole-5-carboxamide O
N

N\ N
H
N O
H

Using the method from Example 56, 3-amino-N-cyclopentyl-N (2-methoxyethyl)-2-(3-oxo-3,4-dihydroquinoxalin-2-yl)-1H-indole-5-carboxamide was obtained as a red solid (50 mg, 39%) from the product of Step 1, Example 307 and 3-vitro-2-(3-oxo-3,4-dihydro-2-quinoxalinyl)-1H-indole-5-carboxylic acid (Example 22). ~H-NMR (DMSO-ds) 8 12.45 (s, 1 H), 10.81 (s, 1 H), 7.94 (s, 1 H), 7.79-7.74 (d, 1 H), 7.46-7.41 (d, 1 H), 7.38-6.98 (m, 6H), 4.24-4.12 (m, 1 H), 3.58-3.20 (m, 7H), 1.82-1.58 (m, 6H), 1.45-1.36 (m, 2H).
LCMS RT =
2.74 min; [M+H]+ = 446.2.
Example 319 Preparation of terl~-butyl 5-f(2-methox r~et_hyl)(methyl amino]I-2lmethoxy~oxo)acetyll-1H
indole-1-carbox I
CHs H3C '-O

Step 1. Preparation of N-(2-methoxyethyl)-N 3-dimethyl-4-nitroaniline CHs HsC.O~N ~ W CHs To a round bottom flask equipped with a reflux condenser was added 5-fluoro-2-nitrotoluene (10 g, 65.0 mmol) in 1-methyl-2-pyrrolidine (150 mL). N-(2-methoxyethyl)methylamine (21 mL, 200 mmol) was added to the stirring solution and the reaction was heated at 80 °C for 3 h. After cooling to rt, the product was purified by chromatography to yield 10.5 g (72%) of a yellow solid. 'H NMR (DMSO-ds): 8 2.62 (s, 3H), 3.01 (s, 3H), 3.24 (s, 3H), 3.40-3.45 (m, 2H), 3.57-3.61 (m, 2H), 6.58-6.62 (m, 2H).
Step 2. N (2-methoxyethy~-N methyl-1 H-indol-5-amine CHs HsC~O~N
N
H
To a round bottom flask equipped with a reflux condenser was charged with N (2-methoxyethyl)-N 3-dimethyl-4-nitroaniline (9.5 g, 42 mmol) and DMF (200 mL).
N,N
dimethylformamide dimethylacetal (6.0 g. 50 mmol) and pyrrolidine (3.6 g, 50 mmol) were added and the reaction was heated at reflux for 3 h. After cooling to rt, the volatile components were removed in vacuo and the oily residue was dissloved in DMF
(100 mL).
The solution was added to 10°lo Pd/C (950 mg ) under argon. The atmosphere was converted to H2 with a balloon and the reaction allowed to stir at rt for 17 h. The H~ was then removed and the mixture filtered through Celite~ under a blanket of argon. The solvents were then removed and the product was purified by chromatography. The desired product was a red oil (7.9 g, 92%). ~H-NMR (DMSO-ds) 8 2.80-2.83 (m, 4H), 3.22 (s, 3H), 2.39-2.43 (m, 2H), 2.46-2.52 (m, 2H), 6.22-6.24 (m, 1 H), 6.72-6.76 (d, 1 H), 6.81 (s, 1 H), 7.18-7.23 (m, 2H), 10.61 (br s, 1 H); l-CMS RT = 0.27 min; [M+H]* =
205.09.
Stea 3. Preparation of tert-but~i[(2-methoxyeth~l~met~l)aminol-1H-indole-1-carboxylate H3C.O~N
N
O\ /CH3 H C~CH3 Using the method described in Example 12 Step 1, tent-butyl 5-[(2-methoxyethyl)(methyl)amino]-1H indole-1-carboxylate was obtained as a coloress solid (7.2 g, 61 %) from N (2-methoxyethyl)-N methyl-1 H indol-5-amine (7.8 g, 38 mmol). ' H-NMR (DMSO-d6) b 1.63 (s, 9H), 2.90(s, 3H), 3.21 (s, 3H), 3.40-3.45 (m, 4H), 6.43-6.46 (m, 1 H), 6.75-6.84 (m, 2H), 7.46-7.50 (d, 1 H), 7.78-7.83 (d, 1 H).
Step 4. Preparation of tert butyl 5-[(2-methoxyeth r~l (methyl amino-2-fmethoxy(oxo acety,-1H-indole-1-carboxylate CH3 p H3C.O~N ~ ~ O
~ N O
~O
O~
HsC~CH3 Using the method described in Example 18 Step 2, tent butyl 5-[(2-methoxyethyl)(methyl)amino]-2-[methoxy(oxo)acetyl]-1 H-indole-1-carboxylate was obtained as an oil (3.6 g, 80%) from tert butyl 5-[(2-methoxyethyl)(methyl)amino]-1H-indole-1-carboxylate (3.5 g, 12 mmol). ~H-NMR (DMSO-ds) 8 1.59 (s, 9H), 3.93 (s, 3H), 3.21 (s, 3H), 3.41-3.58 (m, 4H), 6.85 (m, 1 H), 7.05-7.13 (d, 1 H), 7.25 (s, 1 H), 7.75-7.79 (d, 1 H).

Step 5 Preparation of 3-f5-f(2-methoxyethyl)(methyl)amino]-1H indol-2-yl'~-6,7-dimethylauinoxalin-2(1 H -one ~O

Using the method described in Example 12 Step 3, 3-(5-[(2-methoxyethyl)(methyl)amino]-1H indol-2-yl}-6,7-dimethylquinoxalin-2(1H)-one was obtained as a red powder (204 mg, 88°I°) from tert-butyl 5-[(2-methoxyethyl)(methyl)amino]-2-[methoxy(oxo)acetyl]-1H-indole-1-carboxylate (240 mg, 0.62 mmol) and 1,2-diamino-4,5-dimethylbenzene (69 mg, 0.64 mmol). 'H-NMR
(DMSO-ds) 82.35 (s, 6H), 2.83 (s, 3H), 3.20 (s, 3H), 3.38-3.51 (m, 4H), 6.80-6.85 (m, 1 H), 7.09 (s, 1 H), 7.36-7.40 (d, 1 H), 7.55-7.61 (1 H), 11.19 (s, 1 H), 12.41 (s, 1 H);
LCMS RT = 1.86 min;
[M+H]+ = 377.46.
Example 336-337 Preparation of 2-f7-(4-fluorophenyl)-3-oxo-3 4-dihydroquinoxalin-2-yll-1 H-indole-5-carbonitrile and 2-f6-(4-fluorophenyl)-3-oxo-3,4-dihYdroauinoxalin-2-yll-1H indole-5-carbonitrile F
I
H a F

Step 1 Preparation of (4'-fluoro-3-nitrobiphen~yl amine F
~ I ~. NOz I/

N2 was bubbled through a solution of 4-bromo-6-nitroaniline (3.0 g, 14 mmol) in DME (25 mL) for 10 min before 1,1'-bis(diphenylphosphino-ferrocene) dichloropalladium (II), complex with CH2C12 (1:1) (0.60 g, 0.69 mmol), 1.OM solution of Na2C03 (35 mL, 35 mmol), and 4-fluorophenylboronic acid (2.0 g, 15mmol) were added. The reaction mixture was bubbled with nitrogen for an additional 10 min and then heated at 60 °C for 1 h. The reaction was quenched with water, extracted with EtOAc (3x). The combined organic layers were washed with water, brine, dried (MgS04), and concentrated to obtain a crude residue which was chromatograghed with hexane/EtOAc=3/1 to provide 2.8 g (88%) of the product as an orange solid.'H-NMR (DMSO-d6) 8 8.16 (s 1H), 7.75-7.73 (d, 1H), 7.68-7.54 (m, 2H), 7.53 (s, 2H), 7.27-7.11 (m, 2H), 7.09-7.08 (d, 1 H).
Step 2. Preparation of 4'-fluorobiphenyl-3,4-diamine F

To a dry flask was added 10% Pd/C (0.013 g) under argon. MeOH (100 mL) and (4'-fluoro-3-nitrobiphenyl-4-yl)amine (2.71 g, 11.7 mmol) were added before the atmosphere was converted to hydrogen and the mixture stirred at rt overnight.
The reaction mixture was filtered through Celite, washed with MeOH, and concentrated to provide 2.26 g (96%) of a purplish solid. ~H-NMR (DMSO-d6) 8 7.47-7.44 (m, 2H), 7.17-7.13 (m, 2H), 6.78 (s, 1 H), 6.67-6.64 (d, 1 H), 6.55-6.53 (d, 1 H), 4.59-4.54 (d, 4H). LCMS
RT = 1.74 min; [M+H]+ = 203.2.
Step 3. Preparation of 2-f7-(4-fluorophenyl)-3-oxo-3.4-dihydroauinoxalin-2-yll-1H-indole-5-carbonitrile and 2-f6-(4-fluorophen~rl-)-3-oxo-3,4-dihydroauinoxalin-2-yl]-1H-indole-5-N
F
_ H v F

A solution of 4'-fluorobiphenyl-3,4-diamine (2.28 g, 11.3 mmol) and 2-[methoxy(oxo)acetyl]-1H-indole (5) (2.33 g, 10.3 mmol) in AcOH (10 mL) was heated at 100 °C overnight. The reaction mixture was cooled to rt and diluted with water. The precipitant yellow solid was filtered, wasf~ed with water (5x), and dried in an oven to provide 3.11 g (80%) of a yellow solid. ~H-NMR (DMSO-ds) S 12.83-12.79 (d, 1 H), 12.21-carbonitrile 12.19 (d, 1 H), 8.24 (d, 1 H), 8.05-7.64 (m, 6H), 7.55-7.32 (m, 4H). LCMS RT =
3.49 min;
[M+H]+ = 381.3.
Example 354 Prei~,aration ofi 3-amino-N (2-methoxyeth rl -N meth I-2- 3-oxo-3,4-dihydroauinoxalin 2-yl)-1 H-indole-5-sulfonamide H~N~ ~ CHs ~~N
H
N O
H
Stea 1. Preparation of 2-(3-chloroguinoxalin-2-yl)-N-(2-methox e~~ N methyl-1 H-indole-5-sulfonamide n O
-N

A vial charged with bis(diphenylphosphino)ferrocenepalladium(II) chloride (0.164 g, 0.220 mmol) was added 2,3-dichloroquinoxaline (0.669 g, 3.36 mmol), (5-{[(2-methoxyethyl)(methyl)amino]sulfonyl}-1 H-indol-2-yl)boronic acid (0.700 g, 2.24 mmol), and NaHC03 (0.951 g, 8.97 mmol), followed by DME (5 mL). Water (0.5 mL, bubbled with nitrogen for 10 minutes) was added to the reaction and the mixture was heated to 75 °C for 1 h. An additonal 10 mol% of Pd was added and the mixture was stirred 1.5 h.
Upon consumption of the boronic acid the reaction was concentrated under vacuum and the residue was purified by HPLC to provide 0.300 g of a brown solid (31%). 'H
NMR
(DMSO-d6) 8 12.39 (s, 1 H), 8.22 (d, 1 H), 8.20 (dd, 1 H), 8.08 (dd, 1 H), 7.98-7.89 (m, 2H), 7.74 (dd, 1 H), 7.61 (dd, 1 H), 3.46 (t, 2H), 3.23 (s, 3H), 3.13 (t, 2H), 2.72 (s, 3H); LCMS
RT = 3.34 min; [M+H]=431.1.

Step 2 Preparation of N-~-methoxyethyl)-N-methyl-2-(3-oxo-3,4-dihydroauinoxalin-2 yl)-1 H-indole-5-sulfonamide O'O-N

/
N\
N O
H
2-(3-chloroquinoxalin-2-yl)-N (2-methoxyethyl)-N methyl-1 H-indole-5-sulfonamide (0.280 g, 0.650 mmol) was dissolved in AcOH (20 mL) and was heated at reflux (130 °C) for 18 h. The solvent was removed under the vacuum and the residue was taken up in EtOAc.
The organic layer was washed with sat. NaHC03 and concentrated to afford the product as a red solid (0.250 g, 93%).'H NMR (DMSO-d6) 8 8.15 (s, 1H), 7.98 (s, 1H), 7.83 (dd, 1 H), 7.71 (s, 1 H), 7.69 (d, 1 H), 7.56-7.52 (m, 2H), 7.34 (d, 1 H), 3.44 (t, 2H), 3.21 (s, 3H), 3.10 (t, 2H), 2.68 (s, 3H); LCMS RT = 2.71 min; [M+H]=413.6.
Step 3 Preparation of N-!2-methoxyethyl~-N methyl-3-nitro-2-(3-oxo-3,4-dihydroquinoxalin-2yl)-1H-indole-5-sulfonamide O..O_N
OWN CHs \ /
\ N\
N O
H
Using the method described in Example 2, N (2-methoxyethyl)-N methyl-3-nitro-2-(3-oxo-3,4-dihydroquinoxalin-2-yl)-1 H-indole-5-sulfonamide was obtained as a dark yellow solid (0.085 g, 76%) from N (2-methoxyethyl)-N methyl-2-(3-oxo-3,4-dihydroquinoxalin-2-yl)-1H indole-5-sulfonamide (0.100 g, 0.240 mmol). This material was taken on without purification or characterization.

Step 4. Pre~~aration of 3-amino-N-(2-methox ey thy_I)-N methyl-2-(3-oxo-3,4-dihydroauinoxalin-2-yl)-1H indole-5-sulfonamide -N

I
i IV V
H
Using the method described in Example 3, N-(2-methoxyethyl)-N-methyl-2-(3-oxo-3,4-dihydroquinoxalin-2-yl)-1H-indole-5-sulfonamide was obtained as a red solid (0.012 g, 17%) from N (2-methoxyethyl)-IV methyl-3-vitro-2-(3-oxo-3,4-dihydroquinoxalin-2-yl)-1H-indole-5-sulfonamide (0.085 g, 0.160 mmol).'H NMR (DMSO-d6) 8 12.50 (s, 1H), 11.16 (s, 1 H), 8.40 (s, 1 H), 7.79 (dd, 1 H), 7.63 (d, 1 H), 7.47 (dd, 1 H), 7.35-7.31 (m, 1 H), 7.26-7.23 (m, 2H), 3.44 (t, 2H), 3.12 (s, 3H), 3.09 (t, 2H), 2.71 (s, 3H); LCMS RT
= 2.59 min;
[M+H]=428.5.
Example 375 Preparation of f3-amino-2-(3-oxo-3,4-dihydrog_uinoxalin-2-yl)-1H-indol-5 vllmethyl phenylcarbamate O
-N
O H
HEN -~ N~ H~
a N O
H

Step 1 Preparation of f3-nitro-2-(3-oxo-3 4-dihydroauinoxalin-2-yl)-1H-indol-5-yllmethyl phen~carbamate O., ~,~-. H
OzN ~
\ ~y H
a N O
H
To a solution of 3-(5-(hydroxymethyl)-3-nitro-1 H-indol-2-yl]quinoxalin-2(1 H)-one (Example 156, 0.100 g, 0.290 mmol) in anhydrous DMF (5 mL) at rt was added phenylisocyanate (0.193 g, 1.62 mmol) and the amber solution was stirred at 80 °C for 24 h. The reaction was diluted with CH2CI2 (20 mL) and purified by silica gel chromatography (hexane/EtOAc) to give 0.099 g of a yellow solid (72°I°). TLC: Rf = 0.80 (50°l° hexane/EtOAc); LC-MS (ESI): [M+H]+ = 456.2 and [M+Na]+ =
478.1 @ RT = 3.48 min.
Step 2 Preparation of f3-amino-2-(3-oxo-3 4-dihydroauinoxalin-2-yl)-1H-indol-5-yllmethyl phenylcarbamate O
-N
O H
HZN
I \. N\ H
a N O
H
A suspension of the [3-nitro-2-(3-oxo-3,4-dihydroquinoxalin-2-yl)-1H-indol-5-yl]methyl phenylcarbamate (0.040 g, 0.09 mmol) in glacial AcOH (12 mL) was sonicated for 1 h before iron powder (325 mesh, 0.100 g, 1.79 mmol) added to the very fine yellow suspension. The mixture was stirred at rt for 2 h under nitrogen. The red suspension was quenched by adding it slowly to sat. NaHC03 (300 mL). The mixture was extracted with EtOAc (2 x 300 mL). The combined organic layers were dried (Na2S04), filtered, and concentrated in vacuo to give 0.026 g of a red solid (70%). TLC: Rf = 0.61 (50%
hexanelEtOAc); LC-MS (ESI): (M+H]+ = 426.2 @ RT = 2.87 min.

H
Example 418 Preparation of cyclohexyl 3-amino-2-(3-oxo-3,4-dihydroctuinoxalin-2-yl)-1 H-indole-5-carbox I
O
O
HZN
N~ H~
N O
To a solution of SOC12 (20.0 mL, 272 mmol) was added 3-vitro-2-(3-oxo-3,4-dihydroquinoxalin-2-yl)-1 H-indole-5-carboxylic acid (Example 22, 250 mg, 0.710 mmol) at rt and the resulting brown suspension was heated at 85 °C for 4 h. The suspension was concentrated under reduced pressure and the residue dried for 24 h in vacuo to give 262 mg of 3-vitro-2-(3-oxo-3,4-dihydroquinoxalin-2-yl)-1 N-indole-5-carbonyl chloride as a light yellow solid. To a 250 mL rb flask was placed 3-vitro-2-(3-oxo-3,4-dihydroquinoxalin-2-yl)-1 H indole-5-carbonyl chloride (0.07 g, 0.19 mmol) and CH2CI2 (3 mL). To this was added cyclohexanol (0.03 mL, 0.38 mmol) and Et3N (0.03 mL, 0.21 ) and the reaction was allowed to stir at 60 °C for 18 h. SnCl2 (0.43 g, 1.9 mmol) was added and the reaction was allowed to stir at 60 °C for 12 h. The reaction was diluted with water (30 mL) and DMF (100mL). The mixture was extracted with EtOAc (3x100 mL) and the combined organics were dried (NazS04) and purified by HPLC. The combined fractions were concentrated to provide 0.026 g of a red solid (33%).'H NMR (DMSO-d6) b12.55 (s, 1H), 11.19 (s, 1 H), 8.56 (s, 1 H), 7.78 (m, 1 H), 7.54 (d, 1 H), 7.36 (m, 1 H), 7.27 (m, 1 H), 4.93 (m, 1 H), 1.98-1.55 (m, 10H); LCMS RT = 3.38 min; [M+H]=403.3.
Variations of the compounds of the invention can be readily prepared using the processes described above, or by other standard chemical processes known in the art, by employing appropriate starting materials that are readily available and/or are already described herein.
Generally, a desired salt of a compound of this invention can be prepared in situ during the final isolation and purification of a compound by means well known in the art.
For example, a desired salt can be prepared by separately reacting the purified compound in its free base or free acid form with a suitable organic or inorganic acid, or suitable organic or inorganic base, respectively, and isolating the salt thus formed. In the case of basic compounds, for example, the free base is treated with anhydrous HCI in a suitable solvent such as THF, and the salt isolated as a hydrochloride salt.
In the case of acidic compounds, the salts may be obtained, for example, by treatment of the free acid with anhydrous ammonia in a suitable solvent such as ether and subsequent isolation of the ammonium salt. These methods are conventional and would be readily apparent to one skilled in the art.
Esters of the compounds identified herein can be obtained by conventional means, for example, by reaction of a carboxylic acid compound with an alcohol facilitated by an acid catalyst, or by reaction of the carboxylic acid compound and alcohol under Mitsunobu conditions. These methods are conventional and would be readily apparent to one skilled in the art.
The purification of isomers of a compound of this invention, and the separation of said isomeric mixtures can be accomplished by standard techniques known in the art.
Compositions of the comaounds of this invention The compounds of this invention can be utilized to achieve the desired pharmacological effect by administration to a patient in need thereof in an appropriately formulated pharmaceutical composition. A patient, for the purpose of this invention, is a mammal, including a human, in need of treatment (including prophylactic treatment) for the particular condition or disease. Therefore, the present invention includes pharmaceutical compositions that are comprised of a pharmaceutically acceptable carrier and a pharmaceutically effective amount of a compound, or salt or ester thereof, of the present invention. A pharmaceutically acceptable carrier is any carrier that is relatively non-toxic and innocuous to a patient at concentrations consistent with effective activity of the active ingredient so that any side effects ascribable to the carrier do not vitiate the beneficial effects of the active ingredient. A pharmaceutically effective amount of compound is that amount which produces a result or exerts an influence on the particular condition being treated. The compounds of the present invention can be administered with pharmaceutically-acceptable carriers well known in the art using any effective conventional dosage unit forms, including immediate, slow and timed release preparations, orally, parenterally, topically, nasally, ophthalmically, otically, sublingually, rectally, vaginally, and the like.
For oral administration, the compounds can be formulated into solid or liquid preparations such as capsules, pills, tablets, troches, lozenges, melts, powders, solutions, suspensions, or emulsions, and may be prepared according to methods known to the art for the manufacture of pharmaceutical compositions. The solid unit dosage forms can be a capsule which can be of the ordinary hard- or soft-shelled gelatin type containing, for example, surfactants, lubricants, and inert fillers such as lactose, sucrose, calcium phosphate, and corn starch.
In another embodiment, the compounds of this invention may be tableted with conventional tablet bases such as lactose, sucrose and cornstarch in combination with binders such as acacia, corn starch or gelatin, disintegrating agents intended to assist the break-up and dissolution of the tablet following administration such as potato starch, alginic acid, corn starch, and guar gum, gum tragacanth, acacia, lubricants intended to improve the flow of tablet granulation and to prevent the adhesion of tablet material to the surfaces of the tablet dies and punches, for example talc, stearic acid, or magnesium, calcium or zinc stearate, dyes, coloring agents, and flavoring agents such as peppermint, oil of wintergreen, or cherry flavoring, intended to enhance the aesthetic qualities of the tablets and make them more acceptable to the patient. Suitable excipients for use in oral liquid dosage forms include dicalcium phosphate and diluents such as water and alcohols, for example, ethanol, benzyl alcohol, and polyethylene alcohols, either with or without the addition of a pharmaceutically acceptable surfactant, suspending agent or emulsifying agent. Various other materials may be present as coatings or to otherwise modify the physical form of the dosage unit. For instance tablets, pills or capsules may be coated with shellac, sugar or both.
Dispersible powders and granules are suitable for the preparation of an aqueous suspension. They provide the active ingredient in admixture with a dispersing or wetting agent, a suspending agent and one or more preservatives. Suitable dispersing or wetting agents and suspending agents are exemplified by those already mentioned above.
Additional excipients, for example those sweetening, flavoring and coloring agents described above, may also be present.
The pharmaceutical compositions of this invention may also be in the form of oil-in-water emulsions. The oily phase may be a vegetable oil such as liquid paraffin or a mixture of vegetable oils. Suitable emulsifying agents may be (1) naturally occurring gums such as gum acacia and gum tragacanth, (2) naturally occurring phosphatides such as soy bean and lecithin, (3) esters or partial esters derived form fatty acids and hexitol anhydrides, for example, sorbitan monooleate, (4) condensation products of said partial esters with ethylene oxide, for example, polyoxyethylene sorbitan monooleate.
The emulsions may also contain sweetening and flavoring agents.
Oily suspensions may be formulated by suspending the active ingredient in a vegetable oil such as, for example, arachis oil, olive oil, sesame oil or coconut oil, or in a mineral oil such as liquid paraffin. The oily suspensions may contain a thickening agent such as, for example, beeswax, hard paraffin, or cetyl alcohol. The suspensions may also contain one or more preservatives, for example, ethyl or n-propyl p-hydroxybenzoate; one or more coloring agents; one or more flavoring agents; and one or more sweetening agents such as sucrose or saccharin.
Syrups and elixirs may be formulated with sweetening agents such as, for example, glycerol, propylene glycol, sorbitol or sucrose. Such formulations may also contain a demulcent, and preservative, such as methyl and propyl parabens and flavoring and coloring agents.
The compounds of this invention may also be administered parenterally, that is, subcutaneously, intravenously, intraocularly, intrasynovially, intramuscularly, or interperitoneally, as injectable dosages of the compound in a physiologically acceptable diluent with a pharmaceutical carrier which can be a sterile liquid or mixture of liquids such as water, saline, aqueous dextrose and related sugar solutions, an alcohol such as ethanol, isopropanol, or hexadecyl alcohol, glycols such as propylene glycol or polyethylene glycol, glycerol ketals such as 2,2-dimethyl-1,1-dioxolane-4-methanol, ethers such as polyethylene glycol) 400, an oil, a fatty acid, a fatty acid ester or, a fatty acid glyceride, or an acetylated fatty acid glyceride, with or without the addition of a pharmaceutically acceptable surfactant such as a soap or a detergent, suspending agent such as pectin, carbomers, methycellulose, hydroxypropylmethylcellulose, or carboxymethylcellulose, or emulsifying agent and other pharmaceutical adjuvants.
Illustrative of oils which can be used in the parenteral formulations of this invention are those of petroleum, animal, vegetable, or synthetic origin, for example, peanut oil, soybean oil, sesame oil, cottonseed oil, corn oil, olive oil, petrolatum and mineral oil.
Suitable fatty acids include oleic acid, stearic acid, isostearic acid and myristic acid.
Suitable fatty acid esters are, for example, ethyl oleate and isopropyl myristate. Suitable soaps include fatty acid alkali metal, ammonium, and triethanolamine salts and suitable detergents include cationic detergents, for example dimethyl dialkyl ammonium halides, alkyl pyridinium halides, and alkylamine acetates; anionic detergents, for example, alkyl, aryl, and olefin sulfonates, alkyl, olefin, ether, and monoglyceride sulfates, and sulfosuccinates; non-ionic detergents, for example, fatty amine oxides, fatty acid alkanolamides, and poly(oxyethylene-oxypropylene)s or ethylene oxide or propylene oxide copolymers; and amphoteric detergents, for example, alkyl-beta-aminopropionates, and 2-alkylimidazoline quarternary ammonium salts, as well as mixtures.
The parenteral compositions of this invention will typically contain from about 0.5% to about 25% by weight of the active ingredient in solution.
Preservatives and buffers may also be used advantageously. In order to minimize or eliminate irritation at the site of injection, such compositions may contain a non-ionic surfactant having a hydrophile-lipophife balance (HLB) of from about 12 to about 17. The quantity of surfactant in such formulation ranges from about 5% to about 15% by weight.
The surfactant can be a single component having the above HLB or can be a mixture of two or more components having the desired HLB.
Illustrative of surfactants used in parenteral formulations are the class of polyethylene sorbitan fatty acid esters, for example, sorbitan monooleate and the high molecular weight adducts of ethylene oxide with a hydrophobic base, formed by the condensation of propylene oxide with propylene glycol.
The pharmaceutical compositions may be in the form of sterile injectable aqueous suspensions: Such suspensions may be formulated according to known methods using suitable dispersing or wetting agents and suspending agents such as, for example, sodium carboxymethylcellulose, methylcellulose, hydroxypropylmethyl-cellulose, sodium alginate, polyvinylpyrrolidone, gum tragacanth and gum acacia; dispersing or wetting agents which may be a naturally occurring phosphatide such as lecithin, a condensation product of an alkylene oxide with a fatty acid, for example, polyoxyethylene stearate, a condensation product of ethylene oxide with a long chain aliphatic alcohol, for example, heptadeca-ethyleneoxycetanol, a condensation product of ethylene oxide with a partial ester derived form a fatty acid and a hexitol such as polyoxyethylene sorbitol monooleate, or a condensation product of an ethylene oxide with a partial ester derived from a fatty acid and a hexitol anhydride, for example polyoxyethylene sorbitan monooleate.
The sterile injectable preparation may also be a sterile injectable solution or suspension in a non-toxic parenterally acceptable diluent or solvent. Diluents and solvents that may be employed are, for example, water, Ringer's solution, isotonic sodium chloride solutions and isotonic glucose solutions. In addition, sterile fixed oils are conventionally employed as solvents or suspending media. For this purpose, any bland, fixed oil may be employed including synthetic mono- or diglycerides. In addition, fatty acids such as oleic acid can be used in the preparation of injectables.
A composition of the invention may also be administered in the form of suppositories for rectal administration of the drug. These compositions can be prepared by mixing the drug with a suitable non-irritation excipient which is solid at ordinary temperatures but liquid at the rectal temperature and will therefore melt in the rectum to release the drug. Such material are, for example, cocoa butter and polyethylene glycol.
Another formulation employed in the methods of the present invention employs transdermal delivery devices ("patches"). Such transdermal patches may be used to provide continuous or discontinuous infusion of the compounds of the present invention in controlled amounts. The construction and use of transdermal patches for the delivery of pharmaceutical agents is well known in the art (see, e.g., US Patent No.
5,023,252, issued June 11, 1991, incorporated herein by reference). Such patches may be constructed for continuous, pulsatile, or on demand delivery of pharmaceutical agents.
Controlled release formulations for parenteral administration include liposomal, polymeric microsphere and polymeric gel formulations which are known in the art.
It may be desirable or necessary to introduce the pharmaceutical composition to the patient via a mechanical delivery device. The construction and use of mechanical delivery devices for the delivery of pharmaceutical agents is well known in the art. Direct techniques for, for example, administering a drug directly to the brain usually involve placement of a drug delivery catheter into the patient's ventricular system to bypass the blood-brain barrier. One such implantable delivery system, used for the transport of agents to specific anatomical regions of the body, is described in US Patent No.
5,011,472, issued April 30, 1991.
The compositions of the invention can also contain other conventional pharmaceutically acceptable compounding ingredients, generally referred to as carriers or diluents, as necessary or desired. Conventional procedures for preparing such compositions in appropriate dosage forms can be utilized. Such ingredients and procedures include those described in the following references, each of which is incorporated herein by reference; Powell, M.F. et al, "Compendium of Excipients for Parenteral Formulations" PDA Journal of Pharmaceutical Science & Technology 1998, 52(5), 238-311; Strickley, R.G "Parenteral Formulations of Small Molecule Therapeutics Marketed in the United States (1999)-Part-1" PDA Journal of Pharmaceutical Science &
Technology 1999, 53(6), 324-349; and Nema, S. et al, "Excipients and Their Use in Injectable Products" PDA Journal of Pharmaceutical Science & Technology 1997, 51 (4), 166-171.
Commonly used pharmaceutical ingredients which can be used as appropriate to formulate the composition for its intended route of administration include:
acidifying agents (examples include but are not limited to acetic acid, citric acid, fumaric acid, hydrochloric acid, nitric acid);
alkalinizing agents (examples include but are not limited to ammonia solution, ammonium carbonate, diethanolamine, monoethanolamine, potassium hydroxide, sodium borate, sodium carbonate, sodium hydroxide, triethanolamine, trolamine);
adsorbents (examples include but are not limited to powdered cellulose and activated charcoal);

aerosol propellants (examples include but are not limited to carbon dioxide, CCI2F2, F2CIC-CCIF2 and CCIF3);
air displacement agents (examples include but are not limited to nitrogen and argon);
antifungal preservatives (examples include but are not limited to benzoic acid, butylparaben, ethylparaben, methylparaben, propylparaben, sodium benzoate);
antimicrobial preservatives (examples include but are not limited to benzalkonium chloride, benzethonium chloride, benzyl alcohol, cetylpyridinium chloride, chlorobutanol, phenol, phenyfethyl alcohol, phenylmercuric nitrate and thimerosal);
antioxidants (examples include but are not limited to ascorbic acid, ascorbyl palmitate, butylated hydroxyanisole, butylated hydroxytoluene, hypophosphorus acid, monothioglycerol, propyl gallate, sodium ascorbate, sodium bisulfite, sodium formaldehyde sulfoxylate, sodium metabisulfite);
binding materials (examples include but are not limited to block polymers, natural and synthetic rubber, polyacrylates, polyurethanes, silicones, polysiloxanes and styrene-butadiene copolymers);
buffering agents (examples include but are not limited to potassium metaphosphate, dipotassium phosphate, sodium acetate, sodium citrate anhydrous and sodium citrate dihydrate);
carrying agents (examples include but are not limited to acacia syrup, aromatic syrup, aromatic elixir, cherry syrup, cocoa syrup, orange syrup, syrup, corn oil, mineral oil, peanut oil, sesame oil, bacteriostatic sodium chloride injection and bacteriostatic water for injection);
chelating agents (examples include but are not limited to edetate disodium and edetic acid);
colorants (examples include but are not limited to FD&C Red No. 3, FD&G Red No. 20, FD&C Yellow No. 6, FD&C Blue No. 2, D&C Green No. 5, D&C Orange No. 5, D&C Red No. 8, caramel and ferric oxide red);
clarifying agents (examples include but are not limited to bentonite);
emulsifying agents (examples include but are not limited to acacia, cetomacrogol, cetyl alcohol, glyceryl monostearate, lecithin, sorbitan monooleate, polyoxyethylene 50 monostearate);
encapsulating agents (examples include but are not limited to gelatin and cellulose acetate phthalate);
flavorants (examples include but are not limited to anise oil, cinnamon oil, cocoa, menthol, orange oil, peppermint oil and vanillin);

humectants (examples include but are not limited to glycerol, propylene glycol and sorbitol);
levigating agents (examples include but are not limited to mineral oil and glycerin);
oils (examples include but are not limited to arachis oil, mineral oil, olive oil, peanut oil, sesame oil and vegetable oil);
ointment bases (examples include but are not limited to lanolin, hydrophilic ointment, polyethylene glycol ointment, petrolatum, hydrophilic petrolatum, white ointment, yellow ointment, and rose water ointment);
penetration enhancers (transdermal delivery) (examples include but are not limited to monohydroxy or polyhydroxy alcohols, mono-or polyvalent alcohols, saturated or unsaturated fatty alcohols, saturated or unsaturated fatty esters, saturated or unsaturated dicarboxylic acids, essential oils, phosphatidyl derivatives, cephalin, terpenes, amides, ethers, ketones and ureas);
plasticizers (examples include but are not limited to diethyl phthalate and glycerol);
solvents (examples include but are not limited to ethanol, corn oil, cottonseed oil, glycerol, isopropanol, mineral oil, oleic acid, peanut oil, purified water, water for injection, sterile water for injection and sterile water for irrigation);
stiffening agents (examples include but are not limited to cetyl alcohol, cetyl esters wax, microcrystalline wax, paraffin, stearyl alcohol, white wax and yellow wax);
suppository bases (examples include but are not limited to cocoa butter and polyethylene glycols (mixtures);
surfactants (examples include but are not limited to benzalkonium chloride, nonoxynol 10, oxtoxynol 9, polysorbate 80, sodium lauryl sulfate and sorbitan mono-palmitate);
suspending agents (examples include but are not limited to agar, bentonite, carbomers, carboxymethylcellulose sodium, hydroxyethyl cellulose, hydroxypropyl cellulose, hydroxypropyl methylcellulose, kaolin, methylcellulose, tragacanth and veegum);
sweetening agents (examples include but are not limited to aspartame, dextrose, glycerol, mannitol, propylene glycol, saccharin sodium, sorbitol and sucrose);
tablet anti-adherents (examples include but are not limited to magnesium stearate and talc);
tablet binders (examples include but are not limited to acacia, alginic acid, carboxymethylcellulose sodium, compressible sugar, ethylcellulose, gelatin, liquid glucose, methylcellulose, non-crosslinked polyvinyl pyrrolidone, and pregelatinized starch);
tablet and capsule diluents (examples include but are not limited to dibasic calcium phosphate, kaolin, lactose, mannitol, microcrystalline cellulose, powdered cellulose, precipitated calcium carbonate, sodium carbonate, sodium phosphate, sorbitol and starch);
tablet coating agents (examples include but are not limited to liquid glucose, hydroxyethyl cellulose, hydroxypropyl cellulose, hydroxypropyl methyfcellulose, methylcellulose, ethylcellulose, cellulose acetate phthalate and shellac);
tablet direct compression excipients (examples include but are not limited to dibasic calcium phosphate);
tablet disintegrants (examples include but are not limited to alginic acid, carboxymethylcellulose calcium, microcrystalline cellulose, polacrillin potassium, cross-linked polyvinylpyrrolidone, sodium alginate, sodium starch glycollate and starch);
tablet glidants (examples include but are not limited to colloidal silica, corn starch and talc);
tablet lubricants (examples include but are not limited to calcium stearate, magnesium stearate, mineral oil, stearic acid and zinc stearate);
tablet/capsule opaquants (examples include but are not limited to titanium dioxide);
tablet polishing agents (examples include but are not limited to carnuba wax and white wax);
thickening agents (examples include but are not limited to beeswax, cetyl alcohol and paraffin);
tonicity agents (examples include but are not limited to dextrose and sodium chloride);
viscosity increasing agents (examples include but are not limited to alginic acid, bentonite, carbomers, carboxymethylcellulose sodium, methylcellulose, polyvinyl pyrrolidone, sodium alginate and tragacanth); and wetting agents (examples include but are not limited to heptadecaethylene oxycetanol, lecithins, sorbitol monooleate, polyoxyethylene sorbitol monooleate, and polyoxyethylene stearate).
It is believed that one skilled in the art, utilizing the preceding information, can utilize the present invention to its fullest extent. Nevertheless, the following are examples of pharmaceutical formulations that can be used in the method of the present invention.

They are for illustrative purposes only, and are not to be construed as limiting the invention in any way.
Pharmaceutical compositions according to the present invention can be illustrated as follows:
Sterile IV Solution: A 5 mg/mL solution of the desired compound of this invention is made using sterile, injectable water, and the pH is adjusted if necessary.
The solution is diluted for administration to 1 - 2 mg/mL with sterile 5% dextrose and is administered as an IV infusion over 60 min.
Lyophilized aowder for IV administration: A sterile preparation can be prepared with (i) 100 - 1000 mg of the desired compound of this invention as a lypholized powder, (ii) 32- 327 mg/mL sodium citrate, and (iii) 300 - 3000 mg Dextran 40. The formulation is reconstituted with sterile, injectable saline or dextrose 5% to a concentration of 10 to 20 mg/mL, which is further diluted with saline or dextrose 5% to 0.2 - 0.4 mg/mL, and is administered either IV bolus or by IV infusion over 15 - 60 min.
Intramuscular suspension: The following solution or suspension can be prepared, for intramuscular injection:
50 mg/mL of the desired, water-insoluble compound of this invention mg/mL sodium carboxymethylcellulose 4 mg/mL TWEEN 80 9 mg/mL sodium chloride 9 mg/mL benzyl alcohol Hard Shell Capsules: A large number of unit capsules are prepared by filling standard two-piece hard galantine capsules each with 100 mg of powdered active ingredient, 150 mg of lactose, 50 mg of cellulose and 6 mg of magnesium stearate.
Soft Gelatin Capsules: A mixture of active ingredient in a digestible oil such as soybean oil, cottonseed oil or olive oil is prepared and injected by means of a positive displacement pump into molten gelatin to form soft gelatin capsules containing 100 mg of the active ingredient. The capsules are washed and dried. The active ingredient can be dissolved in a mixture of polyethylene glycol, glycerin and sorbitol to prepare a water miscible medicine mix.
Tablets: A large number of tablets are prepared by conventional procedures so that the dosage unit was 100 mg of active ingredient, 0.2 mg. of colloidal silicon dioxide, 5 mg of magnesium stearate, 275 mg of microcrystalline cellulose, 11 mg. of starch, and 98.8 mg of lactose. Appropriate aqueous and non-aqueous coatings may be applied to increase palatability, improve elegance and stability or delay absorption.
Immediate Release Tablets/Caasules: These are solid oral dosage forms made by conventional and novel processes. These units are taken orally without water for immediate dissolution and delivery of the medication. The active ingredient is mixed in a liquid containing ingredient such as sugar, gelatin, pectin and sweeteners.
These liquids are solidified into solid tablets or caplets by freeze drying and solid state extraction techniques. The drug compounds may be compressed with viscoelastic and thermoelastic sugars and polymers or effervescent components to produce porous matrices intended for immediate release, without the need of water.
Method of treating pharmacological disorders The present invention also relates to a method of using the compounds or compositions described herein for the treatment or prevention of, or in the manufacture of a medicament for treating or preventing, mammalian hyper-proliferative disorders. This method comprises administering to a patient (or a mammal) in need thereof, including a human, an amount of a compound, a pharmaceutically acceptable salt or ester thereof, or a composition of this invention which is effective to treat or.prevent the disorder.
Hyper-proliferative disorders include but are not limited to solid tumors, such as cancers of the breast, respiratory tract, brain, reproductive organs, digestive tract, urinary tract, eye, liver, skin, head and neck, thyroid, parathyroid and their distant metastases.
Those disorders also include lymphomas, sarcomas, and leukemias.
The present invention also relates to a method for using the compounds of this invention as prophylactic or chemopreventive agents for prevention of the mammalian hyper-proliferative disorders described herein. This method comprises administering to a mammal in need thereof, including a human, an amount of a compound of this invention, or a pharmaceutically acceptable salt or ester thereof, which is effective to delay or diminish the onset of the disorder.
Examples of breast cancer include, but are not limited to invasive ductal carcinoma, invasive lobular carcinoma, ductal carcinoma in situ, and lobular carcinoma in situ.
Examples of hyper-proliferative disorders of the cardiovacular system include, but are not limited to, restenosis.
Examples of cancers of the respiratory tract include, but are not limited to small-cell and non-small-cell lung carcinoma, as well as bronchial adenoma and pleuropulmonary blastoma.
Examples of brain cancers include, but are not limited to brain stem and hypophtalmic glioma, cerebellar and cerebral astrocytoma, medulloblastoma, ependymoma, as well as neuroectodermal and pineal tumor.

Tumors of nervous system include, but not limited to glioblastoma.
Tumors of the male reproductive organs include, but are not limited to prostate and testicular cancer. Tumors of the female reproductive organs include, but are not limited to endometrial, cervical, ovarian, vaginal, and vulvar cancer, as well as sarcoma of the uterus.
Tumors of the digestive tract include, but are not limited to anal, colon, colorectal, esophageal, gallbladder, gastric, pancreatic, rectal, small-intestine, and salivary gland cancers.
Tumors of the urinary tract include, but are not limited to bladder, penile, kidney, renal pelvis, ureter, and urethral cancers.
Eye cancers include, but are not limited to intraocular melanoma and retinoblastoma.
Examples of liver cancers include, but are not limited to hepatocellular carcinoma (liver cell carcinomas with or without fibrolamellar variant), cholangiocarcinoma (intrahepatic bile duct carcinoma), and mixed hepatocellular cholangiocarcinoma.
Skin cancers include, but are not limited to squamous cell carcinoma, ICaposi's sarcoma, malignant melanoma, Merkel cell skin cancer, and non-melanoma skin cancer.
Head-and-neck cancers include, but are not limited to laryngeal /
hypopharyngeal / nasopharyngeal / oropharyngeal cancer, and lip and oral cavity cancer.
Lymphomas include, but are not limited to AIDS-related lymphoma, non-Hodgkin's lymphoma, cutaneous T-cell lymphoma, Hodgkin's disease, and lymphoma of the central nervous system.
Sarcomas include, but are not limited to sarcoma of the soft tissue, osteosarcoma, malignant fibrous histiocytoma, lymphosarcoma, and rhabdomyosarcoma.
Leukemias include, but are not limited to acute myeloid leukemia, acute lymphoblastic leukemia, chronic lymphocytic leukemia, chronic myelogenous leukemia, and hairy cell leukemia.
These disorders have been well characterized in humans, and also exist with a similar etiology in other mammals which can also be treated by the administration of the compounds andlor pharmaceutical compositions of the present invention.
The utility of the compounds of the present invention can be illustrated, for example, by their activity in vitro in the in vitro tumor cell proliferation assay described below. The link between activity in tumor cell proliferation assays in vitro and anti-tumor activity in the clinical setting has been very well established in the art.
For example, the therapeutic utility of taxol (Silvestrini et al. Stem Cells 1993, 11(6), 528-35), taxotere (Bissery et al. Anti Cancer Drugs 1995, 6(3), 339), and topoisomerase inhibitors (Edelman et al. Cancer Chemother. Pharmacol. 1996, 37(5), 385-93) were demonstrated with the use of in vitro tumor proliferation assays.
The present compounds and compositions exhibit anti-proliferative activity and are thus useful to treat the indications listed above, e.g. indications mediated by hyperproliferative disorders. Indications mediated by hyperproliferative disorders means diseases or conditions whose progression proceeds, at least in part, via proliferation. The following assay is one of the methods by which compound activity relating to treatment of the disorders identified herein can be determined.
In Vitro Tumor Model Assay Measurement of anti-proliferative activity can be evaluated as follows. A
human tumor cell line such as HCT-116, was cultured under conditions recommended by the supplier (CCL-247, American Type Culture Collection, Manassas, VA, USA). To prepare the assay plates cells were removed from the culture dishes as a single cell suspension and plated at 5000 cell/well in a 96-well plate. Test compounds exemplified by Formula 1 above were dissolved in 100% dimethylsulfoxide at a concentration of 10 mmoles/L and diluted to the appropriated concentration such that the final dimethylsulfoxide concentration in the culture media did not exceed 0.25%. The day after cell plating, the test compounds were added to the culture medium at the appropriate dilutions, and the cells with the test compound were allowed to remain in contact under normal cell culture conditions for 72 hours. The inhibitory activity was measured using a CeIITiter-Glo assay kit, using the instructions provided by the manufacture (Promega, Madison, WI, USA).
The % growth inhibition was calculated using the formula % inhibition = (value with test compound / value without test compound) x 100.
Representative compounds of the invention were tested in the above assay and were found to be active.
Additionally, the compounds of this invention are useful in the prevention and/or treatment of, or in the manufacture of a medicament for treating, angiogenesis dependent disorders. A number of diseases are known to be associated with angiogenesis such as, for example, ocular neovascular disease, neovascular glaucoma, diabetic retinopathy, retrolental fibroplasia, hemangiomas, angiofibromas, psoriasis, age-related macula degeneration, haemangioblastoma, haemangioma, pain and inflammatory diseases such as rheumatoid or rheumatic inflammatory diseases including rheumatoid arthritis, as well as neoplastic diseases including, for example, so-called solid tumors and liquid tumors such as leukemias. As angiogenesis inhibitors, the compounds of this inveniton are also useful to control solid tumor growth such as breast, prostate, lung, pancreatic, renal, colon, and cervical cancer, melanoma, tumor metastasis, and the like as are well known in the art.
Tumors smaller than about 1 - 2 mm in diameter may receive oxygen and nutrients through diffusion directly into the tumor cells. However, angiogenesis is regarded as an absolute prerequisite for tumors that grow beyond that diameter. The principal mechanisms that play an important role in inhibition of tumor angiogenesis include inhibition of the growth of blood vessels, especially capillaries, into an avascular resting turmor, resulting in no net tumor growth due to the balance that is achieved between apoptosis and proliferation. Another route to treatment is through decreasing .or preventing the migration of tumor cells throughout the body through the blood stream due to the inhibition of angiogenesis in relation to the tumor. Additionally, endothelial cell growth may be inhibited to aviod the paracrine growth-stimulating effect exerted on the surrounding tissue by the endothelial cells which normally line the blood vessels.
Measurement of anti-angiogenic activity can be evaluated as follows:
Xenogra~ph Tumor Model Assay:
Female Ncr nude mice [laconic Laboratories, Nl°] were inoculated subcutaneously with 5x106 MDA-MB-231 breast tumor cells (NCI, MD) on day 0.
When tumors reached the size about 75 to 150 mm3, tumor-bearing animals were randomly divided into several groups with 10 mice per group and received the treatment with either vehicle or test compounds. All test compounds were formulated in PEG 400:
Ethanol:
50mM methanesulfonic acid (40:10:50, vlv/v) vehicle, and given orally for 14 days. The dosing volumes were 0.1mL-test article/10g body weight or 10 mL/kg. During the course of the study, the length and width of each tumor was measured with electronic calipers every 2 or 3 days, and tumor size was calculated at each measuring time-point based on the formula of [length (mm) x width (mm)2] / 2. Animal body weights were also recorded at the same time. All animals were observed for clinical signs daily after compound administration. At the end of the treatment period, tumors from both control animals and from animals treated with test compounds were resected and fixed in 10%
buffered formalin and imbedded in paraffin. Tissue sections were prepared for immunohistochemistry and stained with anit-CD31 antibodies (sc-1506, Santa Cruz, CA) and developed using an ABC kit (Vector, Burlingame, CA) according to the manufacturer's instructions. The amount of CD31 staining as a percentage of the total area relative to untreated tumors was determined from images of sections using ImagePro Plus (Media Cybernetics, Silver Spring, MD) software.

Representative compounds of the invention were tested in the above assay and were found be active in reducing tumor size and in inhibiting angiogenisis.
Based upon the above~and other standard laboratory techniques known to evaluate compounds useful for the prevention and/or treatment of the diseases or disorders described above by standard toxicity tests and by standard pharmacological assays for the determination of the prevention and/or treatment of the conditions identified above in mammals, and by comparison of these results with the results of known medicaments that are used to treat these conditions, the effective dosage of the compounds of this invention can readily be determined for prevention and/or treatment of each desired indication. The amount of the active ingredient to be administered in the prevention and/or treatment of one of these conditions can vary widely according to such considerations as the particular compound and dosage unit employed, the mode of administration, the duration of treatment (including prophylactic treatment), the age and sex of the patient treated, and the nature and extent of the condition to be prevented and/or treated.
The total amount of the active ingredient to be administered will generally range from about 0.001 mglkg to about 300 mg/kg, and preferably from about 0.10 mg/kg to about 150 mg/kg body weight per day. A unit dosage may contain from about 0.5 mg to about 1500 mg of active ingredient, and can be administered one or more times per day.
The daily dosage for administration by injection, including intravenous, intramuscular, subcutaneous and parenteral injections, and use of infusion techniques will preferably be from 0.01 to 200 mg/kg of total body weight. The daily rectal dosage regimen will preferably be from 0.01 to 200 mg/kg of total body weight. The daily vaginal dosage regimen will preferably be from 0.01 to 200 mg/kg of total body weight. The daily topical dosage regimen will preferably be from 0.1 to 200 mg administered between one to four times daily. The transdermal concentration will preferably be that required to maintain a daily dose of from 0.01 to 200 mg/kg. The daily inhalation dosage regimen will preferably be from 0.01 to 100 mg/kg of total body weight.
Of course the specific initial and continuing dosage regimen for each patient will vary according to the nature and severity of the condition as determined by the attending diagnostician, the activity of the specific compound employed, the age and general condition of the patient, time of administration, route of administration, rate of excretion of the drug, drug combinations, and the like. The desired mode of administration and number of doses of a compound of the present invention or a pharmaceutically acceptable salt or ester or composition thereof can be ascertained by those skilled in the art using conventional prevention and/or treatment tests.

The compounds of this invention can be administered as the sole pharmaceutical agent or in combination with one or more other pharmaceutical agents where the combination causes no unacceptable adverse effects. For example, the compounds of this invention can be combined with other anti-hyper-proliferative or other indication agents, and the like, as well as with admixtures and combinations thereof.
For example, optional anti-hyper-proliferative agents which can be added to the composition include but are not limited to compounds listed on the cancer chemotherapy drug regimens in the 11t" Edition of the Merck Index, (1996), which is hereby incorporated by reference, such as asparaginase, bleomycin, carboplatin, carmustine, chlorambucil, cisplatin, colaspase, cyclophosphamlde, cytarabine, dacarbazine, dactinomycin, daunorubicin, doxorubicin (adriamycine), epirubicin, etoposide, 5-fluorouracil, hexamethylmelamine, hydroxyurea, ifosfamide, irinotecan, leucovorin, lomustine, mechlorethamine, 6-mercaptopurine, mesna, methotrexate, mitomycin C, mitoxantrone, prednisolone, prednisone, procarbazine, raloxifen, streptozocin, tamoxifen, thioguanine, topotecan, vinblastine, vincristine, and vindesine.
Other anti-hyper-proliferative agents suitable for use with the composition of the invention include but are not limited to those compounds acknowledged to be used in the treatment and/or prevention of neoplastic diseases in Goodman and Giiman's The Pharmacological Basis of Therapeufics (Ninth Edition), editor Molinoff et al., pubf. by McGraw-Hill, pages 1225-1287, (1996), which is hereby incorporated by reference, such as aminoglutethimide, L-asparaginase, azathioprine, 5-azacytidine cladribine, busulfan, diethylstilbestrol, 2', 2'-difluorodeoxycytidine, docetaxel, erythrohydroxynonyladenine, ethinyl estradiol, 5-fluorodeoxyuridine, 5-fluorodeoxyuridine monophosphate, fludarabine phosphate, fluoxymesterone, flutamide, hydroxyprogesterone caproate, idarubicin, interferon, medroxyprogesterone acetate, megestrol acetate, melphalan, mitotane, paclitaxel, pentostatin, N-phosphonoacetyl-L-aspartate (PALA), plicamycin, semustine, teniposide, testosterone propionate, thiotepa, trimethylmelamine, uridine, and vinorelbine.
Other anti-hyper-proliferative agents suitable for use with the composition of this invention include but are not limited to other anti-cancer agents such as epothilone, irinotecan, raloxifen and topotecan.
It is believed that one skilled in the art, using the preceding information and information available in the art, can utilize the present invention to its fullest extent.
It should be apparent to one of ordinary skill in the art that changes and modifications can be made to this invention without departing from the spirit or scope of the invention as it is set forth herein.

Claims (14)

What is claimed is:

1. A compound of Formula I
wherein represents a 6 membered aromatic ring containing 0, 1 or 2 N atoms;

R1 and R2 are each independently selected from H, halo, CF3, C(O)R9, (C1-C6)alkyl optionally substituted with up to two substituents selected from OH, (C1-C3)alkoxy, F, and phenyl, (C1-C6)alkoxy optionally substituted with one or two substituents each independently selected from and N[(C1-C3)alkyl]2 where each alkyl is independently optionally substituted up to two times with (C1-C3)alkoxy, NH(C1-C3)alkyl where said alkyl is optionally substituted with up to two substitutents each selected independently from OH, F, (C1-C3)alkoxy, N[(C1-C3)alkyl]2, NH(C1-C3)alkyl, phenyl, pyrrolidinyl, and N[(C1-C3)alkyl]2 where each alkyl is independently optionally substituted with up to two substitutents each selected independently from OH, F, phenyl, and (C1-C3)alkoxy, said alkoxy being optionally substituted with pyrrolidinyl optionally substituted up to two times with N[(C1-C3)alkyl]2, phenyl optionally substituted with up to two substitutents each selected independently from (C1-C3)alkyl, (C1-C3)alkoxy, halo, CF3, and CN, with the proviso that when contains 1 or 2 N atoms, R1 and R2 must each be H, and, R1 and R2 together with the adjacent C atoms to which they are attached form a ring selected from benzo, dioxolo and imidazo, said imidazo being optionally substituted up to two times with (C1-C3)alkyl, with the proviso that R1 and R2 together with the adjacent C atoms to which they are attached form a ring only when ~ contains no N atoms;
R3 is selected from H, (C1-C4)alkyl, OH, NO2, NH2, NH(C1-C4)alkyl, NHC(O)(C1-C4)alkyl and NHC(O)phenyl, said phenyl being optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, (C1-C3)alkoxy, halo, CF3, and CN;
R4 is selected from H, OH, halo, CN, C(O)R6, S(O)2R7, OSi[(C1-C4)alkyl]3, tetrazolyl, thienyl, pyrrolyl, pyrimidinyl, oxazolyl, furanyl, (C1-C6)alkyl, (C2-C6)alkenyl or (C2-C6)alkynyl, each optionally substituted with OH, F, OC(O)NHphenyl, NHC(O)(C1-C3)alkyl, C(O)NH2, C(O)NH(C1-C3)alkyl, C(O)N[(C1-C3)alkyl]2, (C1-C3)alkoxy optionally substituted up to two times with (C1-C3)alkoxy, NHC(O)NH(C1-C3)alkyl where said alkyl is optionally substituted with up to two substituents independently selected from OH, (C1-C3)alkoxy, F and phenyl, NHC(O)NHphenyl where said phenyl is optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, (C1-C3)alkoxy, halo, CF3, CN, and NHC(O)N[(C1-C3)alkyl]2 where each alkyl is independently optionally substituted up to two times with (C1-C3)alkoxy, NH-phenyl, said phenyl being optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, (C1-C3)alkoxy, halo, CN, and N[(C1-C3)alkyl]2 where each alkyl is independently optionally substituted up to two times with (C1-C3)alkoxy, phenyl optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, (C1-C3)alkoxy, halo, CN, CF3, and pyrrolidinyl optionally substituted up to two times with N[(C1-C3)alkyl]2, (C1-C6)alkoxy optionally substituted with up to two substituents independently selected from (C1-C3)alkoxy, pyrrolidinyl, and N[(C1-C3)alkyl]2 where each alkyl is independently optionally substituted with up to two substituents independently selected from OH, F, (C1-C3)alkoxy and phenyl, N[(C1-C4)alkyl]2 where each of said alkyl groups are independently optionally substituted with up to two substituents independently selected from OH, (C1-C3)alkyl, F, (C1-C3)alkoxy, and phenyl, oxadiazolyl optionally substituted up to two times with (C1-C3)alkyl, phenyl optionally substituted with up to two substituents independently selected from (C1-C3)alkoxy, CN, (C1-C3)alkyl, halo, C(O)(C1-C3)alkyl optionally substituted with up to two substituents independently selected from (C1-C3)alkoxy, OH, (C1-C3)alkoxy, F, and phenyl, and C(O)N[(C1-C3)alkyl]2 where each of said alkyl groups are independently optionally substituted up to two times with (C1-C3)alkoxy, pyridyl optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, C(O)N[(C1-C3)alkyl]2 where each of said alkyl groups are independently optionally substituted up to two times with (C1-C3)alkoxy, and O-pyridyl optionally substituted with up to two substituents independently selected from CF3, halo, and (C1-C3)alkyl;
R5 is selected from H, halo, CN, (C1-C6)alkoxy, and (C1-C6)alkyl;
R6 is selected from OH, NHR10, O-(C3-C6)cycloakyl, (C1-C3)alkoxy, O-(C2-C6)alkenyl, O-(C3-C6)alkynyl, (C1-C6)alkyl optionally substituted with up to two substituents independently selected from OH, (C1-C3)alkoxy, F, and phenyl, N[(C1-C4)alkyl]2 where each of said alkyl groups are independently optionally substituted with up to two substituents independently selected from OH, CN, N[(C1-C4)alkyl]2, (C1-C3)alkoxy, S(O)2-phenyl, S(O)2(C1-C3)alkyl, phenyl, furyl, tetrahydrofuryl, (C3-C6)cycloalkyl, and pyridyl, N[(C1-C3)alkyl]R8where [(C1-C3)alkyl] is optionally substituted up to two times with (C1-C3)alkoxy, N[(C3-C6)cycloalkyl](C1-C3)alkyl where said alkyl is substituted with up to two substituents independently selected from (C1-C3)alkoxy, OH, CN, N[(C1-C4)alkyl]2, S(O)2-phenyl, S(O)2(C1-C3)alkyl, phenyl, furyl, tetrahydrofuryl, (C5-C6)cycloalkyl, and pyridyl, pyrrolidinyl optionally substituted with up to two substituents independently selected from NH2, NH(C1-C3)alkyl, N[(C1-C4)alkyl]2, C(O)NH2, NHC(O)(C1-C3)alkyl, NHS(O)2(C1-C3)alkyl, pyridyl, N[(C1-C3)alkyl]C(O)NH(C1-C3)alkyl, N[(C1-C3)alkyl]C(O)(C1-C3)alkyl, and (C1-C3)alkyl optionally substituted with up to two substituents independently selected from N[(C1-C4)alkyl]2, (C1-C3)alkoxy, and pyrrolidinyl, morpholinyl optionally substituted up to two times with (C1-C3)alkyl, thiomorpholinyl optionally substituted up to two times with (C1-C3)alkyl, piperazinyl optionally substituted with up to two substituents independently selected from pyrazinyl, C(O)NH2, C(O)NH-phenyl, C(O)-furanyl, C(O)(C1-C3)alkyl, C(O)NH(C1-C3)alkyl, C(O)N[(C1-C3)alkyl]R8, S(O)2(C1-C3)alkyl, S(O)2-phenyl, pyridyl optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, CN and CF3, phenyl optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, CN, halo, CF3, and (C1-C3)alkoxy, (C1-C3)alkyl optionally substituted with up to two substituents independently selected from OH, F, phenyl, (C1-C3)alkoxy, N[(C1-C3)alkyl]2, pyrrolinidyl, C(O)-pyrrolidinyl, pyridyl optionally substituted up to two times with (C1-C3)alkoxy, and piperidinyl optionally substituted with up to two substituents independently selected from phenyl, pyridyl, pyrrolidinyl and oxo-dihydrobenzimidazolyl;
R7 is selected from NH2, pyrrolidinyl, NH(C1-C3)alkyl said alkyl being optionally substituted up to two times with (C1-C3)alkoxy, NH-phenyl said phenyl being optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, CN, (C1-C4)alkoxy, halo and CF3, N[(C1-C3)alkyl]2 wherein each alkyl is independently optionally substituted up to two times with (C1-C4)alkoxy, and phenyl optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, (C1-C3)alkoxy, halo, CF3 and CN;
R8 is selected from (C1-C3)alkoxy, pyridyl, piperidinyl, pyranyl and phenyl, where each ring moiety is optionally substituted with up to two substituents independently selected from (C1-C3)alkoxy, and (C1-C3)alkyl;
R9 is selected from (C1-C3)alkyl, (C1-C3)alkoxy, OH, phenyl optionally substituted with (C1-C3)alkyl, (C1-C3)alkoxy, halo, CF3, and CN, N[(C1-C4)alkyl]2 where each of said alkyl groups are independently optionally substituted with OH, CN, N[(C1-C4)alkyl]2, (C1-C4)alkoxy, S(O)2-phenyl, S(O)2(C1-C3)alkyl, phenyl, furyl, tetrahydrofuryl, (C3-C6)cycloalkyl, and pyridyl, and pyrrolidinyl optionally substituted with N[(C1-C3)alkyl]2, and, only when contains no N atoms, R9 is also selected from pyridyl, thienyl, and NHR10;
R10 is selected from H, indolyl, (C1-C4)alkyl optionally substituted with up to two substituents independently selected from OH, F, phenyl, (C1-C4)alkoxy, NHC(O)(C1-C3)alkyl, S-(C1-C3)alkyl, benzimidazolyl, indolyl, thienyl, pyrazolyl, N((C1-C4)alkyl]2 where each alkyl is independently optionally substituted with up to two substituents independently selected from OH, (C1-C3)alkoxy, F, and phenyl, phenyl optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, (C1-C3)alkoxy, CN, halo, CF3, S(O)2(C1-C3)alkyl, S(O)2phenyl, and S(O)2NH2, pyridyl optionally substituted up to two times with CF3, imidazolyl optionally substituted up to two times with (C1-C3)alkyl, furyl optionally substituted up to two times with (C1-C4)alkyl, and pyrrolidinyl optionally substituted with up to two substituents independently selected from (C1-C4)alkoxy, (O), and (C1-C4)alkyl optionally substituted with up to two substituents independently selected from OH, (C1-C3)alkoxy, F, and phenyl, S(O)2-phenyl optionally substituted with up to two substituents independently selected from (C1-C4)alkoxy, (C1-C3)alkyl, halo, and CN, pyrazolyl optionally substituted with up to two substituents independently selected from (C1-C4)alkyl, (C3-C6)cycloalkyl, and phenyl, said phenyl being optionally substituted with up to two substituents independently selected from (C1-C4)alkoxy, (C1-C4)alkyl, halo, CF3, and CN, benzothiazolyl optionally substituted up to two times with (C1-C4)alkyl, thiazolyl, optionally substituted up to two times with (C1-C4)alkyl, thiadiazolyl, optionally substituted with up to two substituents independently selected from CF3, (C3-C6)cycloalkyl, and (C1-C6)alkyl, phenyl optionally substituted with up to two substituents independently selected from CN, halo, CF3, N[(C1-C4)alkyl]2, indolyl, O-pyridyl optionally substituted with C(O)NH(C1-C4)alkyl, (C1-C4)alkyl optionally substituted with up to two substituents independently selected from pyridyl, (C1-C3)alkoxy, F, and phenyl, and (C1-C4)alkoxy optionally substituted with N[(C1-C4)alkyl]2 where one alkyl group is optionally substituted with phenyl, or (C1-C4)alkoxy optionally substituted with pyridyl optionally substituted with phenoxy where said phenoxy is optionally substituted with up to two substituents independently selected from (C1-C4)alkyl and (C1-C4)alkoxy, and indazolyl optionally substituted up to two times with (C1-C4)alkyl;
R11 and R12 are each selected independently from H, F and Cl with the proviso that when one of R11 and R12 is F or Cl, the other must be H;
X is selected from O, S, CH2, and NH, and when X is NH, the H on NH is optionally replaced with pyridyl, pyrazinyl, phenyl, or (C1-C4)alkyl optionally substituted with up to two substituents independently selected from OH, (C1-C3)alkoxy, N[(C1-C3)alkyl]2, C(O)-pyrrolidinyl, N[(C1-C4)alkyl]2, and phenyl said phenyl being optionally substituted with up to two substituents independently selected from CN and (C1-C3)alkoxy, and when X is O, S, or CH2, the moiety is optionally substituted by replacing any H atom in the moiety with (C1-C4)alkyl;
or a pharmaceutically acceptable salt or ester thereof.

2. A compound of claim 1 wherein represents a 6 membered ring containing atoms.

3. A compound of claim 2 wherein R1 and R2 are each independently selected from H, (C1-C3)alkoxy, F, and CF3; R3 is selected from H, NH2, and NHC(O)(C1-C3)alkyl;
R4 is selected from H, halo, (C1-C3)alkoxy, CN, COR6, S(O)AR7, N[(C1-C3)alkyl]2, optionally substituted phenyl and optionally substituted (C1-C4)alkyl; and R5 is selected from H, (C1-C3)alkoxy, F and CN.

4. A compound of claim 3 wherein R5 is selected from H and F; and R4 is selected from H, halo, (C1-C3)alkoxy, CN, COR6, S(O)AR7, N[(C1-C3)alkyl]2, and optionally substituted (C1-C4)alkyl.

5. A compound of claim 4 wherein R1 and R2 are each H; R3 is NH2; R4 is COR6, S(O)AR7, and (C1-C4)alkyl optionally substituted with N[(C1-C3)alkyl]2 and N[(C3-C6)cycloalkyl][(C1-C3)alkyl]; R5 is H; R6 is N[(C1-C3)alkyl]2 and N[(C3-C6)cycloalkyl][(C1-C3)alkyl], R7 is N[(C1-C3)alkyl]2; and R11 and R12 are each H.

6. A compound of claim 1 wherein is 6 membered aromatic ring containing 1 or 2 N atoms.

7. A compound of claim 6 wherein R3 is selected from H, NH2, and NHC(O)(C1-C3)alkyl;
R4 is selected from H, halo, (C1-C3)alkoxy, CN, COR6, S(O)2R7, N[(C1-C3)alkyl]2, optionally substituted phenyl and optionally substituted (C1-C4)alkyl; and R5 is selected from H, (C1-C3)alkoxy, F and CN.

8. A method of treating a hyper-proliferative disorder comprising the administration to a mammal in need thereof of an effective amount of a compound of Formula I

wherein represents a 6 membered aromatic ring containing 0, 1 or 2 N atoms;
R1 and R2 are each independently selected from H, halo, CF3, C(O)R9, (C1-C6)alkyl optionally substituted with up to two substituents selected from OH, (C1-C3)alkoxy, F, and phenyl, (C1-C6)alkoxy optionally substituted with one or two substituents each independently selected from and N[(C1-C3)alkyl]2 where each alkyl is independently optionally substituted up to two times with (C1-C3)alkoxy, NH(C1-C3)alkyl where said alkyl is optionally substituted with up to two substitutents each selected independently from OH, F, (C1-C3)alkoxy, N[(C1-C3)alkyl]2, NH(C1-C3)alkyl, phenyl, pyrrolidinyl, and N[(C1-C3)alkyl]2 where each alkyl is independently optionally substituted with up to two substitutents each selected independently from OH, F, phenyl, and (C1-C3)alkoxy, said alkoxy being optionally substituted with pyrrolidinyl optionally substituted up to two times with N[(C1-C3)alkyl]2, phenyl optionally substituted with up to two substitutents each selected independently from (C1-C3)alkyl, (C1-C3)alkoxy, halo, CF3, and CN, with the proviso that when contains 1 or 2 N atoms, R1 and R2 must each be H, and, R1 and R2 together with the adjacent C atoms to which they are attached form a ring selected from benzo, dioxolo and imidazo, said imidazo being optionally substituted up to two times with (C1-C3)alkyl, with the proviso that R1 and R2 together with the adjacent C atoms to which they are attached form a ring only when contains no N atoms;
R3 is selected from H, (C1-C4)alkyl, OH, NO2, NH2, NH(C1-C4)alkyl, NHC(O)(C1-C4)alkyl and NHC(O)phenyl, said phenyl being optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, (C1-C3)alkoxy, halo, CF3, and CN;

R4 is selected from H, OH, halo, CN, C(O)R6, S(O)2R7, OSi[(C1-C4)alkyl]3, tetrazolyl, thienyl, pyrrolyl, pyrimidinyl, oxazolyl, furanyl, (C1-C6)alkyl, (C2-C6)alkenyl or (C2-C6)alkynyl, each optionally substituted with OH, F, OC(O)NHphenyl, NHC(O)(C1-C3)alkyl, C(O)NH2, C(O)NH(C1-C3)alkyl, C(O)N[(C1-C3)alkyl]2, (C1-C3)alkoxy optionally substituted up to two times with (C1-C3)alkoxy, NHC(O)NH(C1-C3)alkyl where said alkyl is optionally substituted with up to two substituents independently selected from OH, (C1-C3)alkoxy, F and phenyl, NHC(O)NHphenyl where said phenyl is optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, (C1-C3)alkoxy, halo, CF3, CN, and NHC(O)N[(C1-C3)alkyl]2 where each alkyl is independently optionally substituted up to two times with (C1-C3)alkoxy, NH-phenyl, said phenyl being optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, (C1-C3)alkoxy, halo, CN, and N[(C1-C3)alkyl]2 where each alkyl is independently optionally substituted up to two times with (C1-C3)alkoxy, phenyl optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, (C1-C3)alkoxy, halo, CN, CF3, and pyrrolidinyl optionally substituted up to two times with N[(C1-C3)alkyl]2, (C1-C6)alkoxy optionally substituted with up to two substituents independently selected from (C1-C3)alkoxy, pyrrolidinyl, and N[(C1-C3)alkyl]2 where each alkyl is independently optionally substituted with up to two substituents independently selected from OH, F, (C1-C3)alkoxy and phenyl, N[(C1-C4)alkyl]2 where each of said alkyl groups are independently optionally substituted with up to two substituents independently selected from OH, (C1-C3)alkyl, F, (C1-C3)alkoxy, and phenyl, oxadiazolyl optionally substituted up to two times with (C1-C3)alkyl, phenyl optionally substituted with up to two substituents independently selected from (C1-C3)alkoxy, CN, (C1-C3)alkyl, halo, C(O)(C1-C3)alkyl optionally substituted with up to two substituents independently selected from (C1-C3)alkoxy, OH, (C1-C3)alkoxy, F, and phenyl, and C(O)N[(C1-C3)alkyl]2 where each of said alkyl groups are independently optionally substituted up to two times with (C1-C3)alkoxy, pyridyl optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, C(O)N[(C1-C3)alkyl]2 where each of said alkyl groups are independently optionally substituted up to two times with (C1-C3)alkoxy, and O-pyridyl optionally substituted with up to two substituents independently selected from CF3, halo, and (C1-C3)alkyl;
R5 is selected from H, halo, CN, (C1-C6)alkoxy, and (C1-C6)alkyl;
R6 is selected from OH, NHR10, O-(C3-C6)cycloakyl, (C1-C3)alkoxy, O-(C2-C6)alkenyl, O-(C3-C6)alkynyl, (C1-C6)alkyl optionally substituted with up to two substituents independently selected from OH, (C1-C3)alkoxy, F, and phenyl, N[(C1-C4)alkyl]2 where each of said alkyl groups are independently optionally substituted with up to two substituents independently selected from OH, CN, N[(C1-C4)alkyl]2, (C1-C3)alkoxy, S(O)2-phenyl, S(O)2(C1-C3)alkyl, phenyl, furyl, tetrahydrofuryl, (C3-C6)cycloalkyl, and pyridyl, N[(C1-C3)alkyl]R8 where [(C1-C3)alkyl] is optionally substituted up to two times with (C1-C3)alkoxy, N[(C3-C6)cycloalkyl](C1-C3)alkyl where said alkyl is substituted with up to two substituents independently selected from (C1-C3)alkoxy, OH, CN, N[(C1-C4)alkyl]2, S(O)2-phenyl, S(O)2(C1-C3)alkyl, phenyl, furyl, tetrahydrofuryl, (C5-C6)cycloalkyl, and pyridyl, pyrrolidinyl optionally substituted with up to two substituents independently selected from NH2, NH(C1-C3)alkyl, N[(C1-C4)alkyl]2, C(O)NH2, NHC(O)(C1-C3)alkyl, NHS(O)2(C1-C3)alkyl, pyridyl, N[(C1-C3)alkyl]C(O)NH(C1-C3)alkyl, N[(C1-C3)alkyl]C(O)(C1-C3)alkyl, and (C1-C3)alkyl optionally substituted with up to two substituents independently selected from N[(C1-C4)alkyl]2, (C1-C3)alkoxy, and pyrrolidinyl, morpholinyl optionally substituted up to two times with (C1-C3)alkyl, thiomorpholinyl optionally substituted up to two times with (C1-C3)alkyl, piperazinyl optionally substituted with up to two substituents independently selected from pyrazinyl, C(O)NH2, C(O)NH-phenyl, C(O)-furanyl, C(O)(C1-C3)alkyl, C(O)NH(C1-C3)alkyl, C(O)N[(C1-C3)alkyl]R8, S(O)2(C1-C3)alkyl, S(O)2-phenyl, pyridyl optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, CN and CF3, phenyl optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, CN, halo, CF3, and (C1-C3)alkoxy, (C1-C3)alkyl optionally substituted with up to two substituents independently selected from OH, F, phenyl, (C1-C3)alkoxy, N[(C1-C3)alkyl]2, pyrrolinidyl, C(O)-pyrrolidinyl, and pyridyl optionally substituted up to two times with (C1-C3)alkoxy, and piperidinyl optionally substituted with up to two substituents independently selected from phenyl, pyridyl, pyrrolidinyl and oxo-dihydrobenzimidazolyl;
R7 is selected from NH2, pyrrolidinyl, NH(C1-C3)alkyl said alkyl being optionally substituted up to two times with (C1-C3)alkoxy, NH-phenyl said phenyl being optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, CN, (C1-C4)alkoxy, halo and CF3, N[(C1-C3)alkyl]2 wherein each alkyl is independently optionally substituted up to two times with (C1-C4)alkoxy, and phenyl optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, (C1-C3)alkoxy, halo, CF3 and CN;
R8 is selected from (C1-C3)alkoxy, pyridyl, piperidinyl, pyranyl and phenyl, where each ring moiety is optionally substituted with up to two substituents independently selected from (C1-C3)alkoxy, and (C1-C3)alkyl;
R9 is selected from (C1-C3)alkyl, (C1-C3)alkoxy, OH, phenyl optionally substituted with (C1-C3)alkyl, (C1-C3)alkoxy, halo, CF3, and CN, N[(C1-C4)alkyl]2 where each of said alkyl groups are independently optionally substituted with OH, CN, N[(C1-C4)alkyl]2, (C1-C4)alkoxy, S(O)2-phenyl, S(O)2(C1-C3)alkyl, phenyl, furyl, tetrahydrofuryl, (C3-C6)cycloalkyl, and pyridyl, and pyrrolidinyl optionally substituted with N[(C1-C3)alkyl]2, and, only when contains no N atoms, R9 is also selected from pyridyl, thienyl, and NHR10;

R10 is selected from H, indolyl, (C1-C4)alkyl optionally substituted with up to two substituents independently selected from OH, F, phenyl, (C1-C4)alkoxy, NHC(O)(C1-C3)alkyl, S-(C1-C3)alkyl, benzimidazolyl, indolyl, thienyl, pyrazolyl, N[(C1-C4)alkyl]2 where each alkyl is independently optionally substituted with up to two substituents independently selected from OH, (C1-C3)alkoxy, F, and phenyl, phenyl optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, (C1-C3)alkoxy, CN, halo, CF3, S(O)2(C1-C3)alkyl, S(O)2phenyl, and S(O)2NH2, pyridyl optionally substituted up to two times with CF3, imidazolyl optionally substituted up to two times with (C1-C3)alkyl, furyl optionally substituted up to two times with (C1-C4)alkyl, and pyrrolidinyl optionally substituted with up to two substituents independently selected from (C1-C4)alkoxy, (O), and (C1-C4)alkyl optionally substituted with up to two substituents independently selected from OH, (C1-C3)alkoxy, F, and phenyl, S(O)2-phenyl optionally substituted with up to two substituents independently selected from (C1-C4)alkoxy, (C1-C3)alkyl, halo, and CN, pyrazolyl optionally substituted with up to two substituents independently selected from (C1-C4)alkyl, (C3-C6)cycloalkyl, and phenyl, said phenyl being optionally substituted with up to two substituents independently selected from (C1-C4)alkoxy, (C1-C4)alkyl, halo, CF3, and CN, benzothiazolyl optionally substituted up to two times with (C1-C4)alkyl, thiazolyl, optionally substituted up to two times with (C1-C4)alkyl, thiadiazolyl, optionally substituted with up to two substituents independently selected from CF3, (C3-C6)cycloalkyl, and (C1-C6)alkyl, phenyl optionally substituted with up to two substituents independently selected from CN, halo, CF3, N[(C1-C4)alkyl]2, indolyl, O-pyridyl optionally substituted with C(O)NH(C1-C4)alkyl, (C1-C4)alkyl optionally substituted with up to two substituents independently selected from pyridyl, , OH, (C1-C3)alkoxy, F, and phenyl, and (C1-C4)alkoxy optionally substituted with N[(C1-C4)alkyl]2 where one alkyl group is optionally substituted with phenyl, or (C1-C4)alkoxy optionally substituted with pyridyl optionally substituted with phenoxy where said phenoxy is optionally substituted with up to two substituents independently selected from (C1-C4)alkyl and (C1-C4)alkoxy, and indazolyl optionally substituted up to two times with (C1-C4)alkyl;

R11 and R12 are each selected independently from H, F and CI with the proviso that when one of R11 and R12 is F or CI, the other must be H;

X is selected from O, S, CH2, and NH, and when X is NH, the H on NH is optionally replaced with pyridyl, pyrazinyl, phenyl, or (C1-C4)alkyl optionally substituted with up to two substituents independently selected from OH, (C1-C3)alkoxy, N[(C1-C3)alkyl]2, C(O)-pyrrolidinyl, N[(C1-C4)alkyl]2, and phenyl said phenyl being optionally substituted with up to two substituents independently selected from CN and (C1-C3)alkoxy, and when X is O, S, or CH2, the moiety is optionally substituted by replacing any H atom in the moiety with, (C1-C4)alkyl;
or a pharmaceutically acceptable salt or ester thereof.

9. A method according to claim 8 wherein the hyperproliferative disorder is selected from breast cancer, lung cancer, colon cancer, pancreatic cancer, prostate cancer, skin cancer, leukemia, lymphoma, glioblastoma and head and neck cancers.

10. A method according to claim 9 wherein the hyperproliferative disorder is selected from breast cancer, lung cancer, colon cancer and pancreatic cancer.

11. A method of treating a angiogenic disorder comprising the administration to a mammal in need thereof of an effective amount of a compound of Formula I
wherein represents a 6 membered aromatic ring containing 0, 1 or 2 N atoms;
R1 and R2 are each independently selected from H, halo, CF3, C(O)R9, (C1-C6)alkyl optionally substituted with up to two substituents selected from OH, (C1-C3)alkoxy, F, and phenyl, (C1-C6)alkoxy optionally substituted with one or two substituents each ~
independently selected from and N[(C1-C3)alkyl]2 where each alkyl is independently optionally substituted up to two times with (C1-C3)alkoxy, NH(C1-C3)alkyl where said alkyl is optionally substituted with up to two substitutents each selected independently from OH, F, (C1-C3)alkoxy, N[(C1-C3)alkyl]2, NH(C1-C3)alkyl, phenyl, pyrrolidinyl, and N[(C1-C3)alkyl]2 where each alkyl is independently optionally substituted with up to two substitutents each selected independently from OH, F, phenyl, and (C1-C3)alkoxy, said alkoxy being optionally substituted with , pyrrolidinyl optionally substituted up to two times with N[(C1-C3)alkyl]2, phenyl optionally substituted with up to two substitutents each selected independently from (C1-C3)alkyl, (C1-C3)alkoxy, halo, CF3, and CN, with the proviso that when contains 1 or 2 N atoms, R1 and R2 must each be H, and, R1 and R2 together with the adjacent C atoms to which they are attached form a ring selected from benzo, dioxolo and imidazo, said imidazo being optionally substituted up to two times with (C1-C3)alkyl, with the proviso that R1 and R2 together with the adjacent C atoms to which they are attached form a ring only when contains no N atoms;

R3 is selected from H, (C1-C4)alkyl, OH, NO2, NH2, NH(C1-C4)alkyl, NHC(O)(C1-C4)alkyl and NHC(O)phenyl, said phenyl being optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, (C1-C3)alkoxy, halo, CF3, and CN;

R4 is selected from H, OH, halo, CN, C(O)R6, S(O)2R7, OSi[(C1-C4)alkyl]3, tetrazolyl, thienyl, pyrrolyl, pyrimidinyl, oxazolyl, furanyl, (C1-C6)alkyl, (C2-C6)alkenyl or (C2-C6)alkynyl, each optionally substituted with OH, F, OC(O)NHphenyl, NHC(O)(C1-C3)alkyl, C(O)NH2, C(O)NH(C1-C3)alkyl, C(O)N[(C1-C3)alkyl]2,, (C1-C3)alkoxy optionally substituted up to two times with (C1-C3)alkoxy, NHC(O)NH(C1-C3)alkyl where said alkyl is optionally substituted with up to two substituents independently selected from OH, (C1-C3)alkoxy, F and phenyl, NHC(O)NHphenyl where said phenyl is optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, (C1-C3)alkoxy, halo, CF3, CN, and , NHC(O)N[(C1-C3)alkyl]2 where each alkyl is independently optionally substituted up to two times with (C1-C3)alkoxy, NH-phenyl, said phenyl being optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, (C1-C3)alkoxy, halo, CN, and , N[(C1-C3)alkyl]2 where each alkyl is independently optionally substituted up to two times with (C1-C3)alkoxy, phenyl optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, (C1-C3)alkoxy, halo, CN, CF3, and , pyrrolidinyl optionally substituted up to two times with N[(C1-C3)alkyl]2, (C1-C6)alkoxy optionally substituted with up to two substituents independently ~

selected from (C1-C3)alkoxy, pyrrolidinyl, and N[(C1-C3)alkyl]2 where each alkyl is independently optionally substituted with up to two substituents independently selected from OH, F, (C1-C3)alkoxy and phenyl, N[(C1-C4)alkyl]2 where each of said alkyl groups are independently optionally substituted with up to two substituents independently selected from OH, (C1-C3)alkyl, F, (C1-C3)alkoxy, and phenyl, oxadiazolyl optionally substituted up to two times with (C1-C3)alkyl, phenyl optionally substituted with up to two substituents independently selected from (C1-C3)alkoxy, CN, (C1-C3)alkyl, halo, C(O)(C1-C3)alkyl optionally substituted with up to two substituents independently selected from (C1-C3)alkoxy, OH, (C1-C3)alkoxy, F, and phenyl, and C(O)N[(C1-C3)alkyl]2 where each of said alkyl groups are independently optionally substituted up to two times with (C1-C3)alkoxy, pyridyl optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, C(O)N[(C1-C3)alkyl]2 where each of said alkyl groups are independently optionally substituted up to two times with (C1-C3)alkoxy, and O-pyridyl optionally substituted with up to two substituents independently selected from CF3, halo, and (C1-C3)alkyl;
R5 is selected from H, halo, CN, (C1-C6)alkoxy, and (C1-C6)alkyl;
R6 is selected from OH, NHR10, O-(C3-C6)cycloakyl, (C1-C3)alkoxy, O-(C2-C6)alkenyl, O-(C3-C6)alkynyl, (C1-C6)alkyl optionally substituted with up to two substituents independently selected from OH, (C1-C3)alkoxy, F, and phenyl, N[(C1-C4)alkyl]2 where each of said alkyl groups are independently optionally substituted with up to two substituents independently selected from OH, CN, N[(C1-C4)alkyl]2, (C1-C3)alkoxy, S(O)2-phenyl, S(O)2(C1-C3)alkyl, phenyl, furyl, tetrahydrofuryl, (C3-C6)cycloalkyl, and pyridyl, N[(C1-C3)alkyl]R8 where [(C1-C3)alkyl] is optionally substituted up to two times with (C1-C3)alkoxy, N[(C3-C6)cycloalkyl](C1-C3)alkyl where said alkyl is substituted with up to two substituents independently selected from (C1-C3)alkoxy, OH, CN, N[(C1-C4)alkyl]2, S(O)2-phenyl, S(O)2(C1-C3)alkyl, phenyl, furyl, tetrahydrofuryl, (C5-C6)cycloalkyl, and pyridyl, pyrrolidinyl optionally substituted with up to two substituents independently selected from NH2, NH(C1-C3)alkyl, N[(C1-C4)alkyl]2, C(O)NH2, NHC(O)(C1-C3)alkyl, NHS(O)2(C1-C3)alkyl, pyridyl, N[(C1-C3)alkyl]C(O)NH(C1-C3)alkyl, N[(C1-C3)alkyl]C(O)(C1-C3)alkyl, and (C1-C3)alkyl optionally substituted with up to two substituents independently selected from N[(C1-C4)alkyl]2, (C1-C3)alkoxy, and pyrrolidinyl, morpholinyl optionally substituted up to two times with (C1-C3)alkyl, thiomorpholinyl optionally substituted up to two times with (C1-C3)alkyl, piperazinyl optionally substituted with up to two substituents independently selected from pyrazinyl, C(O)NH2, C(O)NH-phenyl, C(O)-furanyl, C(O)(C1-C3)alkyl, C(O)NH(C1-C3)alkyl, C(O)N[(C1-C3)alkyl]R8, S(O)2(C1-C3)alkyl, S(O)2-phenyl, , pyridyl optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, CN and CF3, phenyl optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, CN, halo, CF3, and (C1-C3)alkoxy, (C1-C3)alkyl optionally substituted with up to two substituents independently selected from OH, F, phenyl, (C1-C3)alkoxy, N[(C1-C3)alkyl]2, pyrrolinidyl, C(O)-pyrrolidinyl, , , and pyridyl optionally substituted up to two times with (C1-C3)alkoxy, and piperidinyl optionally substituted with up to two substituents independently selected from phenyl, pyridyl, pyrrolidinyl and oxo-dihydrobenzimidazolyl;

R7 is selected from NH2, pyrrolidinyl, , NH(C1-C3)alkyl said alkyl being optionally substituted up to two times with (C1-C3)alkoxy, NH-phenyl said phenyl being optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, CN, (C1-C4)alkoxy, halo and CF3, N[(C1-C3)alkyl]2 wherein each alkyl is independently optionally substituted up to two times with (C1-C4)alkoxy, and phenyl optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, (C1-C3)alkoxy, halo, CF3 and CN;
R8 is selected from (C1-C3)alkoxy, pyridyl, piperidinyl, pyranyl and phenyl, where each ring moiety is optionally substituted with up to two substituents independently selected from (C1-C3)alkoxy, and (C1-C3)alkyl;

R9 is selected from (C1-C3)alkyl, (C1-C3)alkoxy, OH, , phenyl optionally substituted with (C1-C3)alkyl, (C1-C3)alkoxy, halo, CF3, and CN, N[(C1-C4)alkyl]2 where each of said alkyl groups are independently optionally substituted with OH, CN, N[(C1-C4)alkyl]2, (C1-C4)alkoxy, S(O)2-phenyl, S(O)2(C1-C3)alkyl, phenyl, furyl, tetrahydrofuryl, (C3-C6)cycloalkyl, and pyridyl, and pyrrolidinyl optionally substituted with N[(C1-C3)alkyl]2, and, only when contains no N atoms, R9 is also selected from pyridyl, thienyl, and NHR10;
R10 is selected from H, indolyl, (C1-C4)alkyl optionally substituted with up to two substituents independently selected from OH, F, phenyl, (C1-C4)alkoxy, NHC(O)(C1-C3)alkyl, S-(C1-C3)alkyl, benzimidazolyl, indolyl, thienyl, pyrazolyl, , N[(C1-C4)alkyl]2 where each alkyl is independently optionally substituted with up to two substituents independently selected from OH, (C1-C3)alkoxy, F, and phenyl, phenyl optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, (C1-C3)alkoxy, CN, halo, CF3, S(O)2(C1-C3)alkyl, S(O)2phenyl, and S(O)2NH2, pyridyl optionally substituted up to two times with CF3, imidazolyl optionally substituted up to two times with (C1-C3)alkyl, furyl optionally substituted up to two times with (C1-C4)alkyl, and pyrrolidinyl optionally substituted with up to two substituents independently selected from (C1-C4)alkoxy, (O), and (C1-C4)alkyl optionally substituted with up to two substituents independently selected from OH, (C1-C3)alkoxy, F, and phenyl, S(O)2-phenyl optionally substituted with up to two substituents independently selected from (C1-C4)alkoxy, (C1-C3)alkyl, halo, and CN, pyrazolyl optionally substituted with up to two substituents independently selected from (C1-C4)alkyl, (C3-C6)cycloalkyl, and phenyl, said phenyl being optionally substituted with up to two substituents independently selected from (C1-C4)alkoxy, (C1-C4)alkyl, halo, CF3, and CN, benzothiazolyl optionally substituted up to two times with (C1-C4)alkyl, thiazolyl, optionally substituted up to two times with (C1-C4)alkyl, thiadiazolyl, optionally substituted with up to two substituents independently selected from CF3, (C3-C6)cycloalkyl, and (C1-C6)alkyl, phenyl optionally substituted with up to two substituents independently selected from CN, halo, CF3, N[(C1-C4)alkyl]2, indolyl,, O-pyridyl optionally substituted with C(O)NH(C1-C4)alkyl, (C1-C4)alkyl optionally substituted with up to two substituents independently selected from pyridyl, , OH, (C1-C3)alkoxy, F, and phenyl, and (C1-C4)alkoxy optionally substituted with N[(C1-C4)alkyl]2 where one alkyl group is optionally substituted with phenyl, or (C1-C4)alkoxy optionally substituted with , pyridyl optionally substituted with phenoxy where said phenoxy is optionally substituted with up to two substituents independently selected from (C1-C4)alkyl and (C1-C4)alkoxy, and indazolyl optionally substituted up to two times with (C1-C4)alkyl;
R11 and R12 are each selected independently from H, F and CI with the proviso that when one of R11 and R12 is F or CI, the other must be H;
X is selected from O, S, CH2, and NH, and when X is NH, the H on NH is optionally replaced with pyridyl, pyrazinyl, phenyl, or (C1-C4)alkyl optionally substituted with up to two substituents independently selected from OH, (C1-C3)alkoxy, N[(C1-C3)alkyl]2, C(O)-pyrrolidinyl, N[(C1-C4)alkyl]2, and phenyl said phenyl being optionally substituted with up to two substituents independently selected from CN and (C1-C3)alkoxy, and when X is O, S, or CH2, the moiety is optionally substituted by replacing any H atom in the moiety with (C1-C4)alkyl;
or a pharmaceutically acceptable salt or ester thereof.

12. A method of claim 11 where the angiogenic disorder is selected from diabetic retinopathy, macular degeneration, angiofibromas, a rheumatic inflammatory disease, a neoplastic disease, and a solid tumor growth.

13. A method of claim 12 where the angiogenic disorder is selected from breast cancer, lung cancer, colon cancer, prostate cancer and pancreatic cancer.

14. A pharmaceutical composition comprising a compound of Formula I

wherein represents a 6 membered aromatic ring containing 0, 1 or 2 N atoms;

R1 and R2 are each independently selected from H, halo, CF3, C(O)R9, , (C1-C6)alkyl optionally substituted with up to two substituents selected from OH, (C1-C3)alkoxy, F, and phenyl, (C1-C6)alkoxy optionally substituted with one or two substituents each independently selected from and N[(C1-C3)alkyl]2 where each alkyl is independently optionally substituted up to two times with (C1-C3)alkoxy, NH(C1-C3)alkyl where said alkyl is optionally substituted with up to two substitutents each selected independently from OH, F, (C1-C3)alkoxy, N[(C1-C3)alkyl]2, NH(C1-C3)alkyl, phenyl, pyrrolidinyl, and , N[(C1-C3)alkyl]2 where each alkyl is independently optionally substituted with up to two substitutents each selected independently from OH, F, phenyl, and (C1-C3)alkoxy, said alkoxy being optionally substituted with , pyrrolidinyl optionally substituted up to two times with N[(C1-C3)alkyl]2, phenyl optionally substituted with up to two substitutents each selected independently from (C1-C3)alkyl, (C1-C3)alkoxy, halo, CF3, and CN, with the proviso that when contains 1 or 2 N atoms, R1 and R2 must each be H, and, R1 and R2 together with the adjacent C atoms to which they are attached form a ring selected from benzo, dioxolo and imidazo, said imidazo being optionally substituted up to two times with (C1-C3)alkyl, with the proviso that R1 and R2 together with the adjacent C atoms to which they are attached form a ring only when contains no N atoms;
R3 is selected from H, (C1-C4)alkyl, OH, NO2, NH2, NH(C1-C4)alkyl, NHC(O)(C1-C4)alkyl and NHC(O)phenyl, said phenyl being optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, (C1-C3)alkoxy, halo, CF3, and CN;
R4 is selected from H, OH, halo, CN, C(O)R6, S(O)2R7, OSi[(C1-C4)alkyl]3, tetrazolyl, thienyl, pyrrolyl, pyrimidinyl, oxazolyl, furanyl, (C1-C6)alkyl, (C2-C6)alkenyl or (C2-C6)alkynyl, each optionally substituted with OH, F, OC(O)NHphenyl, NHC(O)(C1-C3)alkyl, C(O)NH2, C(O)NH(C1-C3)alkyl, C(O)N[(C1-C3)alkyl]2, , (C1-C3)alkoxy optionally substituted up to two times with (C1-C3)alkoxy, NHC(O)NH(C1-C3)alkyl where said alkyl is optionally substituted with up to two substituents independently selected from OH, (C1-C3)alkoxy, F and phenyl, NHC(O)NHphenyl where said phenyl is optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, (C1-C3)alkoxy, halo, CF3, CN, and , NHC(O)N[(C1-C3)alkyl]2 where each alkyl is independently optionally substituted up to two times with (C1-C3)alkoxy, NH-phenyl, said phenyl being optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, (C1-C3)alkoxy, halo, CN, and N[(C1-C3)alkyl]2 where each alkyl is independently optionally substituted up to two times with (C1-C3)alkoxy, phenyl optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, (C1-C3)alkoxy, halo, CN, CF3, and pyrrolidinyl optionally substituted up to two times with N[(C1-C3)alkyl]2, (C1-C6)alkoxy optionally substituted with up to two substituents independently selected from (C1-C3)alkoxy, pyrrolidinyl, and N[(C1-C3)alkyl]2 where each alkyl is independently optionally substituted with up to two substituents independently selected from OH, F, (C1-C3)alkoxy and phenyl, N[(C1-C4)alkyl]2 where each of said alkyl groups are independently optionally substituted with up to two substituents independently selected from OH, (C1-C3)alkyl, F, (C1-C3)alkoxy, and phenyl, oxadiazolyl optionally substituted up to two times with (C1-C3)alkyl, phenyl optionally substituted with up to two substituents independently selected from (C1-C3)alkoxy, CN, (C1-C3)alkyl, halo, C(O)(C1-C3)alkyl optionally substituted with up to two substituents independently selected from (C1-C3)alkoxy, OH, (C1-C3)alkoxy, F, and phenyl, and C(O)N[(C1-C3)alkyl]2 where each of said alkyl groups are independently optionally substituted up to two times with (C1-C3)alkoxy, pyridyl optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, C(O)N[(C1-C3)alkyl]2 where each of said alkyl groups are independently optionally substituted up to two times with (C1-C3)alkoxy, and O-pyridyl optionally substituted with up to two substituents independently selected from CF3, halo, and (C1-C3)alkyl;
R5 is selected from H, halo, CN, (C1-C6)alkoxy, and (C1-C6)alkyl;
R6 is selected from OH, NHR10, O-(C3-C6)cycloakyl, (C1-C3)alkoxy, O-(C2-C6)alkenyl, O-(C3-C6)alkynyl, (C1-C6)alkyl optionally substituted with up to two substituents independently selected from OH, (C1-C3)alkoxy, F, and phenyl, N[(C1-C4)alkyl]2 where each of said alkyl groups are independently optionally substituted with up to two substituents independently selected from OH, CN, N[(C1-C4)alkyl]2, (C1-C3)alkoxy, S(O)2-phenyl, S(O)2(C1-C3)alkyl, phenyl, furyl, tetrahydrofuryl, (C3-C6)cycloalkyl, and pyridyl, N[(C1-C3)alkyl]R8 where [(C1-C3)alkyl] is optionally substituted up to two times with (C1-C3)alkoxy, N[(C3-C6)cycloalkyl](C1-C3)alkyl where said alkyl is substituted with up to two substituents independently selected from (C1-C3)alkoxy, OH, CN, N[(C1-C4)alkyl]2, S(O)2-phenyl, S(O)2(C1-C3)alkyl, phenyl, furyl, tetrahydrofuryl, (C5-C6)cycloalkyl, and pyridyl, pyrrolidinyl optionally substituted with up to two substituents independently selected from NH2, NH(C1-C3)alkyl, N[(C1-C4)alkyl]2, C(O)NH2, NHC(O)(C1-C3)alkyl, NHS(O)2(C1-C3)alkyl, pyridyl, N[(C1-C3)alkyl]C(O)NH(C1-C3)alkyl, N[(C1-C3)alkyl]C(O)(C1-C3)alkyl, and (C1-C3)alkyl optionally substituted with up to two substituents independently selected from N[(C1-C4)alkyl]2, (C1-C3)alkoxy, and pyrrolidinyl, morpholinyl optionally substituted up to two times with (C1-C3)alkyl, thiomorpholinyl optionally substituted up to two times with (C1-C3)alkyl, piperazinyl optionally substituted with up to two substituents independently selected from pyrazinyl, C(O)NH2, C(O)NH-phenyl, C(O)-furanyl, C(O)(C1-C3)alkyl, C(O)NH(C1-C3)alkyl, C(O)N[(C1-C3)alkyl]R8, S(O)2(C1-C3)alkyl, S(O)2-phenyl, pyridyl optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, CN and CF3, phenyl optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, CN, halo, CF3, and (C1-C3)alkoxy, (C1-C3)alkyl optionally substituted with up to two substituents independently selected from OH, F, phenyl, (C1-C3)alkoxy, N[(C1-C3)alkyl]2, pyrrolinidyl, C(O)-pyrrolidinyl, and pyridyl optionally substituted up to two times with (C1-C3)alkoxy, and piperidinyl optionally substituted with up to two substituents independently selected from phenyl, pyridyl, pyrrolidinyl and oxo-dihydrobenzimidazolyl;

R7 is selected from NH2, pyrrolidinyl, NH(C1-C3)alkyl said alkyl being optionally substituted up to two times with (C1-C3)alkoxy, NH-phenyl said phenyl being optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, CN, (C1-C4)alkoxy, halo and CF3, N[(C1-C3)alkyl]2 wherein each alkyl is independently optionally substituted up to two times with (C1-C4)alkoxy, and phenyl optionally substituted with up to two substituents independently selected from (C1-C3)alkyl, (C1-C3)alkoxy, halo, CF3 and CN;
R8 is selected from (C1-C3)alkoxy, pyridyl, piperidinyl, pyranyl and phenyl, where each ring moiety is optionally substituted with up to two substituents independently selected from (C1-C3)alkoxy, and (C1-C3)alkyl;

R9 is selected from (C1-C3)alkyl, (C1-C3)alkoxy, OH, phenyl optionally substituted with (C1-C3)alkyl, (C1-C3)alkoxy, halo, CF3, and CN, N[(C1-C4)alkyl]2 where each of said alkyl groups are independently optionally substituted with OH, CN, N[(C1-C4)alkyl]2, (C1-C4)alkoxy, S(O)2-phenyl, S(O)2(C1-C3)alkyl, phenyl, furyl, tetrahydrofuryl, (C3-C6)cycloalkyl, and pyridyl, and pyrrolidinyl optionally substituted with N((C1-C3)alkyl]2, and, only when contains no N atoms, R9 is also selected from pyridyl, thienyl, and NHR10;
R10 is selected from H, indolyl, (C1-C4)alkyl optionally substituted with up to two substituents independently selected from OH, F, phenyl, (C1-C4)alkoxy, NHC(O)(C1-C3)alkyl, S-(C1-C3)alkyl, benzimidazolyl, indolyl, thienyl, pyrazolyl, N[(C1-C4)alkyl]2 where each alkyl is independently optionally substituted with up to two substituents independently selected from OH, (C1-C3)alkoxy, F, and phenyl, phenyl optionally substituted with up to two substituents independently selected from_(C1-C3)alkyl, (C1-C3)alkoxy, CN, halo, CF3, S(O)2(C1-C3)alkyl, S(O)2phenyl, and S(O)2NH2, pyridyl optionally substituted up to two times with CF3, imidazolyl optionally substituted up to two times with (C1-C3)alkyl, furyl optionally substituted up to two times with (C1-C4)alkyl, and pyrrolidinyl optionally substituted with up to two substituents independently selected from (C1-C4)alkoxy, (O), and (C1-C4)alkyl optionally substituted with up to two substituents independently selected from OH, (C1-C3)alkoxy, F, and phenyl, S(O)2-phenyl optionally substituted with up to two substituents independently selected from (C1-C4)alkoxy, (C1-C3)alkyl, halo, and CN, pyrazolyl optionally substituted with up to two substituents independently selected from (C1-C4)alkyl, (C3-C6)cycloalkyl, and phenyl, said phenyl being optionally substituted with up to two substituents independently selected from (C1-C4)alkoxy, (C1-C4)alkyl, halo, CF3, and CN, benzothiazolyl optionally substituted up to two times with (C1-C4)alkyl, thiazolyl, optionally substituted up to two times with (C1-C4)alkyl, thiadiazolyl, optionally substituted with up to two substituents independently selected from CF3, (C3-C6)cycloalkyl, and (C1-C6)alkyl, phenyl optionally substituted with up to two substituents independently selected from CN, halo, CF3, N[(C1-C4)alkyl]2, indolyl, O-pyridyl optionally substituted with C(O)NH(C1-C4)alkyl, (C1-C4)alkyl optionally substituted with up to two substituents independently selected from pyridyl, , OH, (C1-C3)alkoxy, F, and phenyl, and (C1-C4)alkoxy optionally substituted with N[(C1-C4)alkyl]2 where one alkyl group is optionally substituted with phenyl, or (C1-C4)alkoxy optionally substituted with pyridyl optionally substituted with phenoxy where said phenoxy is optionally substituted with up to two substituents independently selected from (C1-C4)alkyl and (C1-C4)alkoxy, and indazolyl optionally substituted up to two times with (C1-C4)alkyl;
R11 and R12 are each selected independently from H, F and Cl with the proviso that when one of R11 and R12 is F or Cl, the other must be H;
X is selected from O, S, CHI, and NH, and when X is NH, the H on NH is optionally replaced with pyridyl, pyrazinyl, phenyl, or (C1-C4)alkyl optionally substituted with up to two substituents independently selected from OH, (C1-C3)alkoxy, N[(C1-C3)alkyl]2, C(O)-pyrrolidinyl, N[(C1-C4)alkyl]2, and phenyl said phenyl being optionally substituted with up to two substituents independently selected from CN and (C1-C3)alkoxy, and when X is O, S, or CH2, the moiety is optionally substituted by replacing any H atom in the moiety with (C1-C4)alkyl;
or a pharmaceutically acceptable salt or ester thereof.