JP2009525279A5 - - Google Patents

Download PDF

Info

Publication number
JP2009525279A5
JP2009525279A5 JP2008552477A JP2008552477A JP2009525279A5 JP 2009525279 A5 JP2009525279 A5 JP 2009525279A5 JP 2008552477 A JP2008552477 A JP 2008552477A JP 2008552477 A JP2008552477 A JP 2008552477A JP 2009525279 A5 JP2009525279 A5 JP 2009525279A5
Authority
JP
Japan
Prior art keywords
mmol
methyl
cln
yloxy
pyrimidin
Prior art date
Legal status (The legal status 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 status listed.)
Pending
Application number
JP2008552477A
Other languages
English (en)
Japanese (ja)
Other versions
JP2009525279A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2007/002315 external-priority patent/WO2007087448A1/en
Publication of JP2009525279A publication Critical patent/JP2009525279A/ja
Publication of JP2009525279A5 publication Critical patent/JP2009525279A5/ja
Pending legal-status Critical Current

Links

JP2008552477A 2006-01-30 2007-01-25 Pparモジュレーターとしてのスピロイミダゾール誘導体 Pending JP2009525279A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US76355706P 2006-01-30 2006-01-30
PCT/US2007/002315 WO2007087448A1 (en) 2006-01-30 2007-01-25 Spiro imidazole derivatives as ppar modulators

Publications (2)

Publication Number Publication Date
JP2009525279A JP2009525279A (ja) 2009-07-09
JP2009525279A5 true JP2009525279A5 (https=) 2010-03-11

Family

ID=37963493

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2008552477A Pending JP2009525279A (ja) 2006-01-30 2007-01-25 Pparモジュレーターとしてのスピロイミダゾール誘導体

Country Status (15)

Country Link
US (1) US20090137610A1 (https=)
EP (1) EP1979355B1 (https=)
JP (1) JP2009525279A (https=)
KR (1) KR20080081359A (https=)
CN (1) CN101374841A (https=)
AT (1) ATE478072T1 (https=)
AU (1) AU2007208156A1 (https=)
BR (1) BRPI0706771A2 (https=)
CA (1) CA2627692A1 (https=)
DE (1) DE602007008524D1 (https=)
ES (1) ES2350608T3 (https=)
PL (1) PL1979355T3 (https=)
PT (1) PT1979355E (https=)
RU (1) RU2008135128A (https=)
WO (1) WO2007087448A1 (https=)

Families Citing this family (32)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2668065A1 (en) 2006-10-30 2008-05-08 Merck & Co., Inc. Spiropiperidine beta-secretase inhibitors for the treatment of alzheimer's disease
EP2025674A1 (de) 2007-08-15 2009-02-18 sanofi-aventis Substituierte Tetrahydronaphthaline, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel
GB0720126D0 (en) 2007-10-15 2007-11-28 Syngenta Participations Ag Chemical compounds
MY159230A (en) 2008-10-02 2016-12-30 Respivert Ltd P38 map kinase inhibitors
JP5670912B2 (ja) 2008-12-11 2015-02-18 レスピバート・リミテツド p38MAPキナーゼ阻害剤
GB0905955D0 (en) 2009-04-06 2009-05-20 Respivert Ltd Novel compounds
FR2944524B1 (fr) * 2009-04-17 2012-11-30 Ipsen Pharma Sas Derives d'imidazolidine-2,4-dione et leur utilisation comme medicament
GB0921730D0 (en) 2009-12-11 2010-01-27 Respivert Ltd Method of treatment
GB0921731D0 (en) 2009-12-11 2010-01-27 Respivert Ltd Theraputic uses
WO2011107494A1 (de) 2010-03-03 2011-09-09 Sanofi Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung
GB201005589D0 (en) 2010-04-01 2010-05-19 Respivert Ltd Novel compounds
EP2556068B1 (en) 2010-04-08 2019-01-23 Respivert Limited P38 map kinase inhibitors
WO2011124923A2 (en) 2010-04-08 2011-10-13 Respivert Limited Novel compounds
BR112012030408A2 (pt) * 2010-05-31 2015-09-29 Syngenta Participations Ag método de melhoramento de culturas
WO2011157827A1 (de) 2010-06-18 2011-12-22 Sanofi Azolopyridin-3-on-derivate als inhibitoren von lipasen und phospholipasen
US8530413B2 (en) 2010-06-21 2013-09-10 Sanofi Heterocyclically substituted methoxyphenyl derivatives with an oxo group, processes for preparation thereof and use thereof as medicaments
WO2011163539A2 (en) * 2010-06-25 2011-12-29 The Johns Hopkins University nAChRα7 AGONISTS AND nAChRα7 ANTAGONISTS FOR TREATING ULCERATIVE COLITIS (UC) AND CROHN'S DISEASE (CD)
TW201221505A (en) 2010-07-05 2012-06-01 Sanofi Sa Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament
TW201215388A (en) 2010-07-05 2012-04-16 Sanofi Sa (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments
TW201215387A (en) 2010-07-05 2012-04-16 Sanofi Aventis Spirocyclically substituted 1,3-propane dioxide derivatives, processes for preparation thereof and use thereof as a medicament
RU2013114390A (ru) 2010-08-31 2014-10-10 СНУ Ар энд ДиБи ФАУНДЕЙШН Применение фетального репрограммирования посредством ppar-дельта-агониста
WO2012120052A1 (de) 2011-03-08 2012-09-13 Sanofi Mit carbozyklen oder heterozyklen substituierte oxathiazinderivate, verfahren zu deren herstellung, diese verbindungen enthaltende arzneimittel und deren verwendung
EP2683705B1 (de) 2011-03-08 2015-04-22 Sanofi Di- und trisubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung
US8828995B2 (en) 2011-03-08 2014-09-09 Sanofi Branched oxathiazine derivatives, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof
US8871758B2 (en) 2011-03-08 2014-10-28 Sanofi Tetrasubstituted oxathiazine derivatives, method for producing them, their use as medicine and drug containing said derivatives and the use thereof
EP2683699B1 (de) 2011-03-08 2015-06-24 Sanofi Di- und trisubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung
WO2013037390A1 (en) 2011-09-12 2013-03-21 Sanofi 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors
EP2760862B1 (en) 2011-09-27 2015-10-21 Sanofi 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors
WO2014076484A1 (en) 2012-11-16 2014-05-22 Respivert Limited Kinase inhibitors
US8652527B1 (en) 2013-03-13 2014-02-18 Upsher-Smith Laboratories, Inc Extended-release topiramate capsules
US9101545B2 (en) 2013-03-15 2015-08-11 Upsher-Smith Laboratories, Inc. Extended-release topiramate capsules
CN113461572B (zh) * 2021-06-30 2023-09-19 江苏慧聚药业股份有限公司 2-(3-溴-5-甲基苯基)乙腈的合成

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2378179A (en) 2001-08-03 2003-02-05 Pantherix Ltd Aromatic sulfonamides and their use in treating bacterial diseases
US7498323B2 (en) * 2003-04-18 2009-03-03 Ono Pharmaceuticals Co., Ltd. Spiro-piperidine compounds and medicinal use thereof

Similar Documents

Publication Publication Date Title
JP2009525279A5 (https=)
KR101934096B1 (ko) 이델라리십의 제조방법
Katrun et al. PhI (OAc) 2 mediated decarboxylative sulfonylation of β-aryl-α, β-unsaturated carboxylic acids: a synthesis of (E)-vinyl sulfones
Ma et al. An efficient synthesis of 2-aminothiophenes via the Gewald reaction catalyzed by an N-methylpiperazine-functionalized polyacrylonitrile fiber
US8394961B2 (en) Method for the preparation of dabigatran
JP2009543861A5 (https=)
CN103497180B (zh) 4-(2,2-二氟-1,3-苯并二氧杂环戊烯-4-基)吡咯-3-腈的合成方法
JP2016027019A (ja) 縮合複素環化合物の製造方法
Borah et al. Efficient synthesis of methyl carbamate via Hofmann rearrangement in the presence of TsNBr2
CN108473463A (zh) 4-((6-(2-(2,4-二氟苯基)-1,1-二氟-2-羟基-3-(1h-1,2,4-三唑-1-基)丙基)吡啶-3-基)氧基)苄腈以及制备方法
JP2008523130A5 (https=)
JP2006514107A5 (https=)
CN103896855B (zh) 一种4-(1-溴代乙基)-5-氟-6-氯嘧啶的合成方法
CN102020634B (zh) 一种n-(氰烷基)苯甲酰胺类化合物的制备方法
JP2015523337A5 (https=)
JP2016539168A5 (https=)
JP2017509581A5 (https=)
JP7232618B2 (ja) アコチアミドの改善された製造方法
JP2010517998A5 (https=)
JP2008201739A (ja) エダラボンの製造方法
JP2007231399A5 (https=)
CN103087033A (zh) 一种多取代氧杂环庚三烯-3(2h)-酮类化合物的合成方法
JP2008533169A5 (https=)
JPWO2017110729A1 (ja) ベンズオキサゾール化合物の製造方法
Wang et al. Concise synthesis of (+)-subersic acid from (−)-Sclareol