CA2582222A1 - Efficient synthesis of 4,5-dihydro-pyrazolo[3,4-c]pyrid-2-ones - Google Patents
Efficient synthesis of 4,5-dihydro-pyrazolo[3,4-c]pyrid-2-ones Download PDFInfo
- Publication number
- CA2582222A1 CA2582222A1 CA002582222A CA2582222A CA2582222A1 CA 2582222 A1 CA2582222 A1 CA 2582222A1 CA 002582222 A CA002582222 A CA 002582222A CA 2582222 A CA2582222 A CA 2582222A CA 2582222 A1 CA2582222 A1 CA 2582222A1
- Authority
- CA
- Canada
- Prior art keywords
- compound
- process according
- ch2ch3
- formula
- ring
- 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.)
- Abandoned
Links
- 0 Bc(cc1)ccc1N(CCc1c2[n](-c3ccccc3)nc1*)C2=O Chemical compound Bc(cc1)ccc1N(CCc1c2[n](-c3ccccc3)nc1*)C2=O 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US61375404P | 2004-09-28 | 2004-09-28 | |
| US60/613,754 | 2004-09-28 | ||
| US63762304P | 2004-12-20 | 2004-12-20 | |
| US60/637,623 | 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 |
| US11/235,647 | 2005-09-26 | ||
| 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 (1)
| Publication Number | Publication Date |
|---|---|
| CA2582222A1 true CA2582222A1 (en) | 2006-04-06 |
Family
ID=36100112
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002582222A Abandoned CA2582222A1 (en) | 2004-09-28 | 2005-09-27 | Efficient synthesis of 4,5-dihydro-pyrazolo[3,4-c]pyrid-2-ones |
Country Status (11)
| Country | Link |
|---|---|
| US (3) | US7304157B2 (enExample) |
| EP (1) | EP1805176A2 (enExample) |
| JP (1) | JP2008514710A (enExample) |
| KR (1) | KR20070067176A (enExample) |
| AU (1) | AU2005289598A1 (enExample) |
| BR (1) | BRPI0516172A (enExample) |
| CA (1) | CA2582222A1 (enExample) |
| IL (1) | IL182147A0 (enExample) |
| MX (1) | MX2007003427A (enExample) |
| NO (1) | NO20071634L (enExample) |
| WO (1) | WO2006036926A2 (enExample) |
Families Citing this family (8)
| 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 |
| TW200738672A (en) * | 2001-12-10 | 2007-10-16 | Bristol Myers Squibb Co | Intermediated for the preparation of 4,5-dihydro-pyrazolo [3,4-c] pyrid-2-ones |
| DE60330749D1 (de) * | 2002-01-21 | 2010-02-11 | Organon Nv | Verfahren zur herstellung von 7-alpha-methylsteroide |
| 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 |
| BRPI0519331A2 (pt) * | 2004-12-15 | 2009-01-20 | Bristol Myers Squibb Co | formas cristalina de um inibidor de fator xa |
| FI20070471A0 (fi) * | 2007-06-13 | 2007-06-13 | Glykos Finland Oy | Ravinnelisäkompositiota |
| CN105384739B (zh) * | 2014-09-02 | 2020-03-20 | 石药集团中奇制药技术(石家庄)有限公司 | 吡唑并[3,4-c]吡啶类衍生物 |
Family Cites Families (8)
| 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 |
| HRP20080382A2 (en) | 2001-09-21 | 2008-12-31 | Bristol-Myers Squibb Company A Delaware (Usa) Corporation | LACTAM-CONTAINING COMPOUNDS AND DERIVATIVES THEREOF AS FACTOR Xa INHIBITORS |
| TW200738672A (en) | 2001-12-10 | 2007-10-16 | Bristol Myers Squibb Co | Intermediated for the preparation of 4,5-dihydro-pyrazolo [3,4-c] pyrid-2-ones |
| US20060069085A1 (en) | 2004-09-28 | 2006-03-30 | Rulin Zhao | Preparation of 4,5-dihydro-pyrazolo[3,4-c]pyrid-2-ones |
| 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 |
| US7388096B2 (en) | 2004-09-28 | 2008-06-17 | Bristol-Myers Squibb Company | Crystalline forms of a factor Xa inhibitor |
| US20060069260A1 (en) * | 2004-09-28 | 2006-03-30 | Huiping Zhang | Preparation of N-aryl pyridones |
-
2005
- 2005-09-26 US US11/235,647 patent/US7304157B2/en not_active Expired - Lifetime
- 2005-09-27 CA CA002582222A patent/CA2582222A1/en not_active Abandoned
- 2005-09-27 AU AU2005289598A patent/AU2005289598A1/en not_active Abandoned
- 2005-09-27 BR BRPI0516172-0A patent/BRPI0516172A/pt not_active Application Discontinuation
- 2005-09-27 WO PCT/US2005/034511 patent/WO2006036926A2/en not_active Ceased
- 2005-09-27 KR KR1020077009650A patent/KR20070067176A/ko not_active Withdrawn
- 2005-09-27 MX MX2007003427A patent/MX2007003427A/es not_active Application Discontinuation
- 2005-09-27 EP EP05805626A patent/EP1805176A2/en not_active Withdrawn
- 2005-09-27 JP JP2007534699A patent/JP2008514710A/ja not_active Withdrawn
-
2007
- 2007-03-22 IL IL182147A patent/IL182147A0/en unknown
- 2007-03-28 NO NO20071634A patent/NO20071634L/no not_active Application Discontinuation
- 2007-08-15 US US11/838,932 patent/US7435821B2/en not_active Expired - Lifetime
- 2007-08-15 US US11/838,926 patent/US7579472B2/en active Active
Also Published As
| Publication number | Publication date |
|---|---|
| US20070282106A1 (en) | 2007-12-06 |
| WO2006036926A2 (en) | 2006-04-06 |
| WO2006036926B1 (en) | 2007-03-15 |
| US7435821B2 (en) | 2008-10-14 |
| EP1805176A2 (en) | 2007-07-11 |
| WO2006036926A3 (en) | 2007-01-18 |
| NO20071634L (no) | 2007-06-21 |
| JP2008514710A (ja) | 2008-05-08 |
| US7579472B2 (en) | 2009-08-25 |
| US20060069119A1 (en) | 2006-03-30 |
| US20080009626A1 (en) | 2008-01-10 |
| MX2007003427A (es) | 2007-05-10 |
| AU2005289598A1 (en) | 2006-04-06 |
| KR20070067176A (ko) | 2007-06-27 |
| US7304157B2 (en) | 2007-12-04 |
| BRPI0516172A (pt) | 2008-08-26 |
| IL182147A0 (en) | 2007-07-24 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FZDE | Discontinued |