JP2009536618A5 - - Google Patents

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Publication number
JP2009536618A5
JP2009536618A5 JP2009506701A JP2009506701A JP2009536618A5 JP 2009536618 A5 JP2009536618 A5 JP 2009536618A5 JP 2009506701 A JP2009506701 A JP 2009506701A JP 2009506701 A JP2009506701 A JP 2009506701A JP 2009536618 A5 JP2009536618 A5 JP 2009536618A5
Authority
JP
Japan
Prior art keywords
phenyl
cyclopropyl
produce
compound
following
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
JP2009506701A
Other languages
English (en)
Japanese (ja)
Other versions
JP2009536618A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2007/066684 external-priority patent/WO2007121390A1/en
Publication of JP2009536618A publication Critical patent/JP2009536618A/ja
Publication of JP2009536618A5 publication Critical patent/JP2009536618A5/ja
Pending legal-status Critical Current

Links

JP2009506701A 2006-04-18 2007-04-16 4−及び5−イミダゾリル環を含むサイトカイン阻害化合物の製造方法及びその中間体 Pending JP2009536618A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US74501006P 2006-04-18 2006-04-18
PCT/US2007/066684 WO2007121390A1 (en) 2006-04-18 2007-04-16 Process for making cytokine inhibiting compounds containing 4- and 5- imidazolyl rings and the intermediates thereof

Publications (2)

Publication Number Publication Date
JP2009536618A JP2009536618A (ja) 2009-10-15
JP2009536618A5 true JP2009536618A5 (cg-RX-API-DMAC7.html) 2010-06-03

Family

ID=38327037

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2009506701A Pending JP2009536618A (ja) 2006-04-18 2007-04-16 4−及び5−イミダゾリル環を含むサイトカイン阻害化合物の製造方法及びその中間体

Country Status (5)

Country Link
US (1) US7858804B2 (cg-RX-API-DMAC7.html)
EP (1) EP2010522A1 (cg-RX-API-DMAC7.html)
JP (1) JP2009536618A (cg-RX-API-DMAC7.html)
CA (1) CA2647266A1 (cg-RX-API-DMAC7.html)
WO (1) WO2007121390A1 (cg-RX-API-DMAC7.html)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BRPI0712795A2 (pt) 2006-07-07 2012-09-04 Boehringer Ingelheim Int derivados de heteroarila substituìdos com fenila e uso dos mesmos como agentes antitumorais
PE20090837A1 (es) * 2007-07-02 2009-07-24 Boehringer Ingelheim Int Nuevos compuestos quimicos
TW201014860A (en) 2008-09-08 2010-04-16 Boehringer Ingelheim Int New chemical compounds
CA2738448A1 (en) 2008-09-29 2010-04-01 Boehringer Ingelheim International Gmbh New chemical compounds
EP2398797B1 (en) 2009-02-17 2013-11-06 Boehringer Ingelheim International GmbH Pyrimido[5,4-d]pyrimidine derivatives for the inhibition of tyrosine kinases
JP5871897B2 (ja) 2010-03-26 2016-03-01 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング ピリジルトリアゾール
WO2011117381A1 (en) 2010-03-26 2011-09-29 Boehringer Ingelheim International Gmbh B-raf kinase inhibitors
US8710055B2 (en) 2010-12-21 2014-04-29 Boehringer Ingelheim International Gmbh Triazolylphenyl sulfonamides as serine/threonine kinase inhibitors
US8889684B2 (en) 2011-02-02 2014-11-18 Boehringer Ingelheim International Gmbh Azaindolylphenyl sulfonamides as serine/threonine kinase inhibitors
US9278951B2 (en) * 2011-04-29 2016-03-08 The University Of Akron Azolium and purinium salt anticancer and antimicrobial agents
WO2013064231A1 (en) 2011-10-31 2013-05-10 Phenex Pharmaceuticals Ag SEVEN-MEMBERED SULFONAMIDES AS MODULATORS OF RAR-RELATED ORPHAN RECEPTOR-GAMMA (RORγ, NR1F3)
NZ708593A (en) 2013-02-27 2018-01-26 Mochida Pharm Co Ltd Novel pyrazole derivative
CN109553591B (zh) * 2019-01-15 2020-12-15 山东安信制药有限公司 一种富马酸喹硫平中间体的制备方法
WO2022188792A1 (zh) * 2021-03-12 2022-09-15 四川科伦博泰生物医药股份有限公司 具有蛋白激酶抑制活性的杂环化合物、包含其的药物组合物及其制备方法和用途

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PT1725544E (pt) * 2004-03-09 2009-07-02 Boehringer Ingelheim Pharma 3-[4-heterociclil-1,2,3-triazol-1-il]-n-aril-benzamidas como inibidores da produção de citocinas para o tratamento de doenças inflamatórias crónicas

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