[go: up one dir, main page]

NO20084326L - Fremgangsmate for fremstilling av [(1R), 2S]-2-aminopropansyre 2-[4-(4-fluor-2-metyl-1H-indol-5-yloksy)-5-metylpyrrolo[2,1-f][1,2,4]triazin-6-yloksy]-1-metyletylester - Google Patents

Fremgangsmate for fremstilling av [(1R), 2S]-2-aminopropansyre 2-[4-(4-fluor-2-metyl-1H-indol-5-yloksy)-5-metylpyrrolo[2,1-f][1,2,4]triazin-6-yloksy]-1-metyletylester

Info

Publication number
NO20084326L
NO20084326L NO20084326A NO20084326A NO20084326L NO 20084326 L NO20084326 L NO 20084326L NO 20084326 A NO20084326 A NO 20084326A NO 20084326 A NO20084326 A NO 20084326A NO 20084326 L NO20084326 L NO 20084326L
Authority
NO
Norway
Prior art keywords
yloxy
methylpyrrolo
indol
fluoro
methyl
Prior art date
Application number
NO20084326A
Other languages
English (en)
Norwegian (no)
Inventor
John E Thornton
Gerard A Crispino
Mourad Hamedi
Thomas L Laporte
Jaan A Pesti
Zhongmin Xu
Paul C Lobben
David K Leahy
Jale Muslehiddinoglu
Chiajen Lai
Lori Ann Spangler
Robert P Discordia
Original Assignee
Bristol Myers Squibb Co
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=38357966&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=NO20084326(L) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co
Publication of NO20084326L publication Critical patent/NO20084326L/no

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Diabetes (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Emergency Medicine (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Endocrinology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
NO20084326A 2006-04-21 2008-10-16 Fremgangsmate for fremstilling av [(1R), 2S]-2-aminopropansyre 2-[4-(4-fluor-2-metyl-1H-indol-5-yloksy)-5-metylpyrrolo[2,1-f][1,2,4]triazin-6-yloksy]-1-metyletylester NO20084326L (no)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US74530006P 2006-04-21 2006-04-21
PCT/US2007/066911 WO2007124332A1 (en) 2006-04-21 2007-04-19 PROCESS FOR THE PREPARATION OF [(1R), 2S]-2-AMINOPROPIONIC ACID 2-[4-(4-FLUORO-2-METHYL-1H-INDOL-5-YLOXY)-5-METHYLPYRROLO[2,1-f][1,2,4]TRIAZIN-6-YLOXY]-1-METHYLETHYL ESTER

Publications (1)

Publication Number Publication Date
NO20084326L true NO20084326L (no) 2008-11-18

Family

ID=38357966

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20084326A NO20084326L (no) 2006-04-21 2008-10-16 Fremgangsmate for fremstilling av [(1R), 2S]-2-aminopropansyre 2-[4-(4-fluor-2-metyl-1H-indol-5-yloksy)-5-metylpyrrolo[2,1-f][1,2,4]triazin-6-yloksy]-1-metyletylester

Country Status (23)

Country Link
US (1) US7671199B2 (da)
EP (1) EP2010538B1 (da)
JP (1) JP5203353B2 (da)
KR (1) KR101423789B1 (da)
CN (1) CN101472927B (da)
AR (1) AR060622A1 (da)
AU (1) AU2007240453B2 (da)
BR (1) BRPI0710691A2 (da)
CA (1) CA2650059A1 (da)
CL (2) CL2007001141A1 (da)
DK (1) DK2010538T3 (da)
EA (1) EA019693B1 (da)
ES (1) ES2399379T3 (da)
HR (1) HRP20130099T1 (da)
IL (1) IL194715A (da)
MX (1) MX2008013232A (da)
NO (1) NO20084326L (da)
PE (1) PE20080193A1 (da)
PL (1) PL2010538T3 (da)
PT (1) PT2010538E (da)
SI (1) SI2010538T1 (da)
TW (1) TWI378100B (da)
WO (1) WO2007124332A1 (da)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1928880A1 (en) * 2005-09-27 2008-06-11 Brystol-Myers Squibb Company Crystalline forms of [(1r), 2s]-2-aminopropionic acid 2-[4-(4-fluoro-2-methyl-1h-indol-5-yloxy)-5-methylpyrrolo[2,1-f][1,2,4]triazin-6-yloxy]-1-methylethyl ester
US20120135875A1 (en) * 2008-02-29 2012-05-31 Bristol-Myers Squibb Company Methods for determining sensitivity to vascular endothelial growth factor receptor-2 modulators
TW201035100A (en) 2008-12-19 2010-10-01 Cephalon Inc Pyrrolotriazines as ALK and JAK2 inhibitors
US11860139B2 (en) 2018-10-08 2024-01-02 Applied Photophysics Limited System and method for analysing the composition of a quenched flow reaction liquid

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6982265B1 (en) * 1999-05-21 2006-01-03 Bristol Myers Squibb Company Pyrrolotriazine inhibitors of kinases
TWI329112B (en) * 2002-07-19 2010-08-21 Bristol Myers Squibb Co Novel inhibitors of kinases
US6933386B2 (en) * 2002-07-19 2005-08-23 Bristol Myers Squibb Company Process for preparing certain pyrrolotriazine compounds
US20050288290A1 (en) * 2004-06-28 2005-12-29 Borzilleri Robert M Fused heterocyclic kinase inhibitors
US7432373B2 (en) * 2004-06-28 2008-10-07 Bristol-Meyers Squibb Company Processes and intermediates useful for preparing fused heterocyclic kinase inhibitors
US7393667B2 (en) * 2005-05-31 2008-07-01 Bristol-Myers Squibb Company Stereoselective reduction process for the preparation of pyrrolotriazine compounds
EP1928880A1 (en) * 2005-09-27 2008-06-11 Brystol-Myers Squibb Company Crystalline forms of [(1r), 2s]-2-aminopropionic acid 2-[4-(4-fluoro-2-methyl-1h-indol-5-yloxy)-5-methylpyrrolo[2,1-f][1,2,4]triazin-6-yloxy]-1-methylethyl ester

Also Published As

Publication number Publication date
TW200808799A (en) 2008-02-16
AU2007240453A1 (en) 2007-11-01
PE20080193A1 (es) 2008-03-10
ES2399379T3 (es) 2013-04-01
MX2008013232A (es) 2008-10-21
CL2010000554A1 (es) 2010-10-15
US20070249610A1 (en) 2007-10-25
JP5203353B2 (ja) 2013-06-05
EA200802171A1 (ru) 2009-08-28
PT2010538E (pt) 2013-02-22
EP2010538B1 (en) 2012-12-05
KR20090008246A (ko) 2009-01-21
HRP20130099T1 (hr) 2013-03-31
BRPI0710691A2 (pt) 2011-08-23
WO2007124332A1 (en) 2007-11-01
AR060622A1 (es) 2008-07-02
CN101472927B (zh) 2012-07-04
US7671199B2 (en) 2010-03-02
CN101472927A (zh) 2009-07-01
EP2010538A1 (en) 2009-01-07
DK2010538T3 (da) 2013-03-18
CA2650059A1 (en) 2007-11-01
EA019693B1 (ru) 2014-05-30
AU2007240453B2 (en) 2012-04-12
TWI378100B (en) 2012-12-01
SI2010538T1 (sl) 2013-06-28
CL2007001141A1 (es) 2008-01-18
PL2010538T3 (pl) 2013-04-30
IL194715A (en) 2013-10-31
KR101423789B1 (ko) 2014-07-30
JP2009534413A (ja) 2009-09-24

Similar Documents

Publication Publication Date Title
EP2457913A3 (en) Heteroaryl compounds, compositions thereof, and methods of treatment therewith
EA200900136A1 (ru) Пирролопиримидины для фармацевтических композиций
WO2009150137A3 (en) Pyrazine derivatives as epithelial sodium channel blockers
ZA200902384B (en) Heteroaryl compounds, compositions thereof, and use thereof as protein kinase inhibitors
WO2007084391A3 (en) Thiazole compounds as protein kinase b ( pkb) inhibitors
WO2008036308A3 (en) Amino-substituted heterocycles, compositions thereof, and methods of treatment therewith
GEP20125537B (en) Derivatives of 1-phenyl-2-pyridinyl alkyl alcohols as phosphodiesterase inhibitors
MY162022A (en) Chemical compounds 637: pyridopyrimidinediones as pde4 inhibitors
WO2007085895A3 (en) Fap inhibitors
JO2848B1 (en) Organic compounds
EA200802050A1 (ru) Новые гетероарилзамещенные ариламинопиридиновые производные в качестве мек ингибиторов
MA29857B1 (fr) Derives de triazolopyridine en tant qu'inhibiteurs de lipases et phospholipases
NO20082730L (no) Morfolinopyrimidinderivater og deres anvendelse i terapi
NO20076371L (no) Fremgangsmate for fremstilling av fenoliske 4-bifenylylazetidin-2-oner
NO20091605L (no) Pyridinonforbindelser
MX2010007714A (es) Piridinas fusionadas activas como inhibidores de c-met.
NO20083642L (no) Dibenzylaminderivater som CETP-inhibitorer
WO2007123939A3 (en) Novel arylamino n-heteraryls as mek inhibitors
WO2008086122A3 (en) Imidazole derivatives as kinesin spindle protein inhibitors (eg-5)
WO2011047055A8 (en) Novel mek inhibitors, useful in the treatment of diseases
WO2008001391A3 (en) Site-specific inhibitors of histone methyltransferase [hmtase] and process of preparation thereof
EA200801008A1 (ru) Гипохолестеринемические соединения
MA32290B1 (fr) Nouvelle classe de spiro pipéridines pour le traitement de maladies neurodégénératives
NO20084326L (no) Fremgangsmate for fremstilling av [(1R), 2S]-2-aminopropansyre 2-[4-(4-fluor-2-metyl-1H-indol-5-yloksy)-5-metylpyrrolo[2,1-f][1,2,4]triazin-6-yloksy]-1-metyletylester
MA33917B1 (fr) Dérivés d'acide carboxylique ayant un cycle oxazolopyrimidine 2,5-substitue

Legal Events

Date Code Title Description
FC2A Withdrawal, rejection or dismissal of laid open patent application