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PE20120321A1 - Indazoles sustituidos con oxazol como inhibidores de pi3-quinasa - Google Patents

Indazoles sustituidos con oxazol como inhibidores de pi3-quinasa

Info

Publication number
PE20120321A1
PE20120321A1 PE2011001881A PE2011001881A PE20120321A1 PE 20120321 A1 PE20120321 A1 PE 20120321A1 PE 2011001881 A PE2011001881 A PE 2011001881A PE 2011001881 A PE2011001881 A PE 2011001881A PE 20120321 A1 PE20120321 A1 PE 20120321A1
Authority
PE
Peru
Prior art keywords
methyl
indazol
oxazol
pyridinyl
oxazole
Prior art date
Application number
PE2011001881A
Other languages
English (en)
Inventor
Julie Nicole Hamblin
Paul Spencer Jones
Nigel James Parr
Suzanne Elaine Keeling
Joelle Le
Charlotte Jane Mitchell
Original Assignee
Glaxo Group Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Glaxo Group Ltd filed Critical Glaxo Group Ltd
Publication of PE20120321A1 publication Critical patent/PE20120321A1/es

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    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/5375—1,4-Oxazines, e.g. morpholine
    • A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
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    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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    • A61K31/4965—Non-condensed pyrazines
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Abstract

SE REFIERE A COMPUESTOS DERIVADOS DE INDAZOLES SUSTITUIDOS CON OXAZOL DE FORMULA (I) DONDE R1 ES HETEROARILO BICICLICO DE 9 O 10 MIEMBROS O PIRIDINILO OPCIONALMENTE SUSTITUIDOS CON ALQUILO(C1-C6), HALOGENO, ENTRE OTROS; R2 Y R3 JUNTO CON EL ATOMO DE N CON EL QUE ESTAN UNIDOS FORMAN UN HETEROCICLILO DE 6 O 7 MIEMBROS OPCIONALMENTE SUSTITUIDO CON ALQUILO(C1-C6); R4 ES H O METILO. SON COMPUESTOS PREFERIDOS: N-[5-[4-(5-{[(2R,6S)-2,6-DIMETIL-4-MORFOLINIL]-METIL}-1,3-OXAZOL-2-IL)-1H-INDAZOL-6-IL]-2-(METILOXI)-3-PIRIDINIL]-METANSULFONAMIDA; N-[5-[4-(5-{[4-(1-METIL-ETIL)-1-PIPERAZINIL]-METIL}-1,3-OXAZOL-2-IL)-1H-INDAZOL-6-IL]-2-(METILOXI)-3-PIRIDINIL]-METANSULFONAMIDA; 6-(1H-INDOL-4-IL)-4-(5-{[4-(1-METIL-ETIL)-1-PIPERAZINIL]-METIL}-1,3-OXAZOL-2-IL)-1H-INDAZOL; ENTRE OTROS. TAMBIEN SE REFIERE A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE LA ACTIVIDAD DE PI3 QUINASAS SIENDO UTILES EN EL TRATAMIENTO DE ASMA, FIBROSIS PULMONAR IDIOPATICA, RINITIS ALERGICA, ESCLEROSIS MULTIPLE
PE2011001881A 2009-04-30 2010-04-28 Indazoles sustituidos con oxazol como inhibidores de pi3-quinasa PE20120321A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US17403309P 2009-04-30 2009-04-30

Publications (1)

Publication Number Publication Date
PE20120321A1 true PE20120321A1 (es) 2012-04-19

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PE2011001881A PE20120321A1 (es) 2009-04-30 2010-04-28 Indazoles sustituidos con oxazol como inhibidores de pi3-quinasa

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US (14) US20120046286A1 (es)
EP (3) EP2424864B1 (es)
JP (1) JP5570589B2 (es)
KR (2) KR101771193B1 (es)
CN (1) CN102459253B (es)
AR (2) AR076435A1 (es)
AU (1) AU2010243613B2 (es)
BR (1) BRPI1016219B8 (es)
CA (1) CA2759476C (es)
CL (1) CL2011002706A1 (es)
CO (1) CO6390057A2 (es)
CR (1) CR20110603A (es)
CY (1) CY1119515T1 (es)
DK (2) DK2899191T3 (es)
DO (1) DOP2011000328A (es)
EA (1) EA021056B1 (es)
ES (3) ES2644724T3 (es)
HR (2) HRP20150173T1 (es)
HU (1) HUE034724T2 (es)
IL (1) IL215803A (es)
JO (1) JO3025B1 (es)
LT (1) LT2899191T (es)
MA (1) MA33304B1 (es)
ME (2) ME02053B (es)
MX (1) MX2011011534A (es)
MY (1) MY160454A (es)
NZ (1) NZ596071A (es)
PE (1) PE20120321A1 (es)
PL (2) PL2424864T3 (es)
PT (2) PT2424864E (es)
RS (2) RS56433B1 (es)
SG (2) SG10201401881QA (es)
SI (2) SI2899191T1 (es)
SM (2) SMT201700481T1 (es)
TW (3) TWI466884B (es)
UA (1) UA101098C2 (es)
UY (1) UY32585A (es)
WO (1) WO2010125082A1 (es)
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JP5502077B2 (ja) 2008-06-05 2014-05-28 グラクソ グループ リミテッド 新規な化合物
WO2009147189A1 (en) 2008-06-05 2009-12-10 Glaxo Group Limited Novel compounds
US8658635B2 (en) 2008-06-05 2014-02-25 Glaxosmithkline Intellectual Property Development Limited Benzpyrazol derivatives as inhibitors of PI3 kinases
JP5656880B2 (ja) 2009-03-09 2015-01-21 グラクソ グループ リミテッドＧｌａｘｏ Ｇｒｏｕｐ Ｌｉｍｉｔｅｄ Ｐｉ３キナーゼの阻害剤としての４−オキサジアゾール−２−イル−インダゾール
UA101098C2 (xx) 2009-04-30 2013-02-25 Глаксо Груп Лимитед Заміщені оксазолом індазоли як інгібітори pi3-кінази$замещенные оксазолом индазолы как ингибиторы pi3-киназы
CN102372675B (zh) * 2010-08-14 2013-12-18 王娜 6-氯-4-碘吲唑及其制备方法与应用
US9102668B2 (en) 2010-09-08 2015-08-11 Glaxo Group Limited Polymorphs and salts
ES2602972T3 (es) * 2010-09-08 2017-02-23 Glaxosmithkline Intellectual Property Development Limited Derivados de indazol para su uso en el tratamiento de infección por virus de la gripe
PL2614058T3 (pl) 2010-09-08 2015-12-31 Glaxosmithkline Ip Dev Ltd Polimorfy i sole n-[5-[4-(5-{[(2r,6s)-2,6-dimetylo-4-morfolinylo]-metylo}-1,3-oksazol-2-ilo)-1h-indazol-6-ilo]-2-(metyloksy)-3-pirydynylo]metanosulfonamidu
GB201018124D0 (en) 2010-10-27 2010-12-08 Glaxo Group Ltd Polymorphs and salts
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