JP2008514710A5 - - Google Patents

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Publication number
JP2008514710A5
JP2008514710A5 JP2007534699A JP2007534699A JP2008514710A5 JP 2008514710 A5 JP2008514710 A5 JP 2008514710A5 JP 2007534699 A JP2007534699 A JP 2007534699A JP 2007534699 A JP2007534699 A JP 2007534699A JP 2008514710 A5 JP2008514710 A5 JP 2008514710A5
Authority
JP
Japan
Prior art keywords
methylene chloride
aprotic solvent
aprotic
solvent
methylene
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.)
Withdrawn
Application number
JP2007534699A
Other languages
English (en)
Japanese (ja)
Other versions
JP2008514710A (ja
Filing date
Publication date
Priority claimed from US11/235,647 external-priority patent/US7304157B2/en
Application filed filed Critical
Publication of JP2008514710A publication Critical patent/JP2008514710A/ja
Publication of JP2008514710A5 publication Critical patent/JP2008514710A5/ja
Withdrawn legal-status Critical Current

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JP2007534699A 2004-09-28 2005-09-27 4,5−ジヒドロ−ピラゾロ[3,4−c]ピリド−2−オン類の効率的合成 Withdrawn JP2008514710A (ja)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US61375404P 2004-09-28 2004-09-28
US63762304P 2004-12-20 2004-12-20
US11/235,647 US7304157B2 (en) 2004-09-28 2005-09-26 Efficient synthesis of 4,5-dihydro-pyrazolo[3,4-c]pyrid-2-ones
PCT/US2005/034511 WO2006036926A2 (en) 2004-09-28 2005-09-27 Efficient synthesis of 4,5-dihydro-pyrazolo[3,4-c]pyrid-2-ones

Publications (2)

Publication Number Publication Date
JP2008514710A JP2008514710A (ja) 2008-05-08
JP2008514710A5 true JP2008514710A5 (US20050137174A1-20050623-C00027.png) 2008-11-13

Family

ID=36100112

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2007534699A Withdrawn JP2008514710A (ja) 2004-09-28 2005-09-27 4,5−ジヒドロ−ピラゾロ[3,4−c]ピリド−2−オン類の効率的合成

Country Status (11)

Country Link
US (3) US7304157B2 (US20050137174A1-20050623-C00027.png)
EP (1) EP1805176A2 (US20050137174A1-20050623-C00027.png)
JP (1) JP2008514710A (US20050137174A1-20050623-C00027.png)
KR (1) KR20070067176A (US20050137174A1-20050623-C00027.png)
AU (1) AU2005289598A1 (US20050137174A1-20050623-C00027.png)
BR (1) BRPI0516172A (US20050137174A1-20050623-C00027.png)
CA (1) CA2582222A1 (US20050137174A1-20050623-C00027.png)
IL (1) IL182147A0 (US20050137174A1-20050623-C00027.png)
MX (1) MX2007003427A (US20050137174A1-20050623-C00027.png)
NO (1) NO20071634L (US20050137174A1-20050623-C00027.png)
WO (1) WO2006036926A2 (US20050137174A1-20050623-C00027.png)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI331526B (en) * 2001-09-21 2010-10-11 Bristol Myers Squibb Pharma Co Lactam-containing compounds and derivatives thereof as factor xa inhibitors
TW200303201A (en) * 2001-12-10 2003-09-01 Bristol Myers Squibb Co Synthesis of 4,5-dihydro-pyrazolo [3,4-c] pyrid-2-ones
TWI322813B (en) * 2002-01-21 2010-04-01 Organon Nv Process for the preparation of 7alpha-methylsteroids
US20060069085A1 (en) * 2004-09-28 2006-03-30 Rulin Zhao Preparation of 4,5-dihydro-pyrazolo[3,4-c]pyrid-2-ones
US7388096B2 (en) * 2004-09-28 2008-06-17 Bristol-Myers Squibb Company Crystalline forms of a factor Xa inhibitor
AR053990A1 (es) * 2004-12-15 2007-05-30 Bristol Myers Squibb Co Formas cristalinas de un compuesto de pirazolpiridina inhibidor de factor xa. composiciones farmaceuticas y procesos de obtencion.
FI20070471A0 (fi) * 2007-06-13 2007-06-13 Glykos Finland Oy Ravinnelisäkompositiota
CA2959987C (en) * 2014-09-02 2023-05-09 Cspc Zhongqi Pharmaceutical Technology (Shijiazhuang) Co., Ltd. Pyrazolo[3,4-c]pyridine compounds and their anti-thrombosis effect

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5423698A (en) * 1994-03-30 1995-06-13 Molex Incorporated Electrical connector system for a video display tube yoke
TWI331526B (en) * 2001-09-21 2010-10-11 Bristol Myers Squibb Pharma Co Lactam-containing compounds and derivatives thereof as factor xa inhibitors
CH1427415H1 (de) 2001-09-21 2023-12-21 Bristol Myers Squibb Holdings Ireland Lactamhaltige verbindungen und ihre derivate als faktor-xa-hemmer
TW200303201A (en) * 2001-12-10 2003-09-01 Bristol Myers Squibb Co Synthesis of 4,5-dihydro-pyrazolo [3,4-c] pyrid-2-ones
US20060069260A1 (en) 2004-09-28 2006-03-30 Huiping Zhang Preparation of N-aryl pyridones
US20060069085A1 (en) * 2004-09-28 2006-03-30 Rulin Zhao Preparation of 4,5-dihydro-pyrazolo[3,4-c]pyrid-2-ones
US7388096B2 (en) 2004-09-28 2008-06-17 Bristol-Myers Squibb Company Crystalline forms of a factor Xa inhibitor
US7396932B2 (en) 2004-09-28 2008-07-08 Bristol-Myers Squibb Company Process for preparing 4,5-dihydro-pyrazolo[3,4-c]pyrid-2-ones

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