CL2009001088A1 - Forma cristalina (ii) de (1r,4r)-4-(1,1-dimetiletilsulfonamido)-n-(5-(trifluorometil) piridin-2-il) ciclohexancarboxamida; procesos de preparacion; utiles como antagonistas del receptor npyy5. - Google Patents
Forma cristalina (ii) de (1r,4r)-4-(1,1-dimetiletilsulfonamido)-n-(5-(trifluorometil) piridin-2-il) ciclohexancarboxamida; procesos de preparacion; utiles como antagonistas del receptor npyy5.Info
- Publication number
- CL2009001088A1 CL2009001088A1 CL2009001088A CL2009001088A CL2009001088A1 CL 2009001088 A1 CL2009001088 A1 CL 2009001088A1 CL 2009001088 A CL2009001088 A CL 2009001088A CL 2009001088 A CL2009001088 A CL 2009001088A CL 2009001088 A1 CL2009001088 A1 CL 2009001088A1
- Authority
- CL
- Chile
- Prior art keywords
- useful
- dimethylethylsulfonamido
- cyclohexanecarboxamide
- pyridin
- trifluoromethyl
- Prior art date
Links
- -1 1,1-dimethylethylsulfonamido Chemical group 0.000 title 1
- 238000002360 preparation method Methods 0.000 title 1
- 239000002464 receptor antagonist Substances 0.000 title 1
- 229940044551 receptor antagonist Drugs 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 2
- 239000005557 antagonist Substances 0.000 abstract 1
- 239000013078 crystal Substances 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- IBBMAWULFFBRKK-UHFFFAOYSA-N picolinamide Chemical compound NC(=O)C1=CC=CC=N1 IBBMAWULFFBRKK-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/01—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
- C07C311/02—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C311/07—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a ring other than a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
Abstract
Procedimiento de preparación de compuestos derivados de piridinamida y sus cristales; compuestos intermediarios; útiles como antagonistas del receptor NPYY5.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2008122154 | 2008-05-08 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CL2009001088A1 true CL2009001088A1 (es) | 2011-06-17 |
Family
ID=41264672
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CL2009001088A CL2009001088A1 (es) | 2008-05-08 | 2009-05-06 | Forma cristalina (ii) de (1r,4r)-4-(1,1-dimetiletilsulfonamido)-n-(5-(trifluorometil) piridin-2-il) ciclohexancarboxamida; procesos de preparacion; utiles como antagonistas del receptor npyy5. |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US20110060145A1 (es) |
| EP (1) | EP2275410A4 (es) |
| JP (2) | JP4756565B2 (es) |
| KR (1) | KR101278359B1 (es) |
| CN (1) | CN102015647A (es) |
| AR (1) | AR071695A1 (es) |
| AU (1) | AU2009245113A1 (es) |
| CA (1) | CA2723133A1 (es) |
| CL (1) | CL2009001088A1 (es) |
| MX (1) | MX2010011835A (es) |
| RU (1) | RU2010144412A (es) |
| TW (1) | TWI369350B (es) |
| WO (1) | WO2009136617A1 (es) |
| ZA (1) | ZA201007364B (es) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SG174488A1 (en) * | 2009-03-19 | 2011-10-28 | Shionogi & Co | Solid preparation containing npy y5 receptor antagonist |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2311479T3 (es) * | 1999-11-26 | 2009-02-16 | SHIONOGI & CO., LTD. | Antagonistas de npy-y5. |
| CN101104598B (zh) * | 2002-03-12 | 2011-06-15 | 盐野义制药株式会社 | 反式-4-氨基-1-环己烷羧酸衍生物的制备方法 |
| JP4636525B2 (ja) * | 2004-03-12 | 2011-02-23 | 塩野義製薬株式会社 | トランス−4−アミノ−1−シクロヘキサンカルボン酸エチルエステルの塩およびその製造方法 |
| BRPI0609529A2 (pt) * | 2005-03-31 | 2010-04-13 | Shionogi & Co | processo para a preparação de compostos derivados de sulfamato-carboxilato e composto |
| JP4895230B2 (ja) * | 2006-09-28 | 2012-03-14 | 塩野義製薬株式会社 | 4−スルフィニルアミノ−1−シクロヘキサンカルボン酸の塩の製造方法 |
-
2009
- 2009-05-06 CL CL2009001088A patent/CL2009001088A1/es unknown
- 2009-05-07 JP JP2010511076A patent/JP4756565B2/ja not_active Expired - Fee Related
- 2009-05-07 MX MX2010011835A patent/MX2010011835A/es unknown
- 2009-05-07 CN CN2009801164557A patent/CN102015647A/zh active Pending
- 2009-05-07 TW TW098115070A patent/TWI369350B/zh not_active IP Right Cessation
- 2009-05-07 AU AU2009245113A patent/AU2009245113A1/en not_active Abandoned
- 2009-05-07 CA CA2723133A patent/CA2723133A1/en not_active Abandoned
- 2009-05-07 US US12/990,782 patent/US20110060145A1/en not_active Abandoned
- 2009-05-07 RU RU2010144412/04A patent/RU2010144412A/ru not_active Application Discontinuation
- 2009-05-07 EP EP09742741A patent/EP2275410A4/en not_active Withdrawn
- 2009-05-07 KR KR1020107027280A patent/KR101278359B1/ko not_active Expired - Fee Related
- 2009-05-07 WO PCT/JP2009/058608 patent/WO2009136617A1/ja not_active Ceased
- 2009-05-07 AR ARP090101658A patent/AR071695A1/es not_active Application Discontinuation
-
2010
- 2010-10-14 ZA ZA2010/07364A patent/ZA201007364B/en unknown
-
2011
- 2011-04-05 JP JP2011084062A patent/JP5234856B2/ja not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| ZA201007364B (en) | 2012-01-25 |
| JPWO2009136617A1 (ja) | 2011-09-08 |
| AR071695A1 (es) | 2010-07-07 |
| EP2275410A1 (en) | 2011-01-19 |
| CN102015647A (zh) | 2011-04-13 |
| JP4756565B2 (ja) | 2011-08-24 |
| JP5234856B2 (ja) | 2013-07-10 |
| TW200948783A (en) | 2009-12-01 |
| KR20110004898A (ko) | 2011-01-14 |
| CA2723133A1 (en) | 2009-11-12 |
| JP2011178790A (ja) | 2011-09-15 |
| TWI369350B (en) | 2012-08-01 |
| RU2010144412A (ru) | 2012-06-20 |
| WO2009136617A1 (ja) | 2009-11-12 |
| KR101278359B1 (ko) | 2013-06-25 |
| US20110060145A1 (en) | 2011-03-10 |
| EP2275410A4 (en) | 2012-05-09 |
| AU2009245113A1 (en) | 2009-11-12 |
| MX2010011835A (es) | 2010-11-25 |
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