ATE183995T1 - Herstellung von mit enantiomer angereicherten ortho-substituierten alpha, alpha-diaromatischen methanolen - Google Patents
Herstellung von mit enantiomer angereicherten ortho-substituierten alpha, alpha-diaromatischen methanolenInfo
- Publication number
- ATE183995T1 ATE183995T1 AT96903991T AT96903991T ATE183995T1 AT E183995 T1 ATE183995 T1 AT E183995T1 AT 96903991 T AT96903991 T AT 96903991T AT 96903991 T AT96903991 T AT 96903991T AT E183995 T1 ATE183995 T1 AT E183995T1
- Authority
- AT
- Austria
- Prior art keywords
- alpha
- diaromatic
- methanols
- enantiomer
- ortho
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 abstract 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C231/00—Preparation of carboxylic acid amides
- C07C231/16—Preparation of optical isomers
- C07C231/18—Preparation of optical isomers by stereospecific synthesis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C213/00—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton
- C07C213/08—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton by reactions not involving the formation of amino groups, hydroxy groups or etherified or esterified hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/56—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having carbon atoms of carboxamide groups bound to carbon atoms of carboxyl groups, e.g. oxamides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
- C07C37/001—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by modification in a side chain
- C07C37/002—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by modification in a side chain by transformation of a functional group, e.g. oxo, carboxyl
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/07—Optical isomers
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/390,255 US5646330A (en) | 1995-02-17 | 1995-02-17 | Production of enantiomerically enriched ortho-substituted α,α-diaromatic methanols |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ATE183995T1 true ATE183995T1 (de) | 1999-09-15 |
Family
ID=23541741
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT96903991T ATE183995T1 (de) | 1995-02-17 | 1996-02-06 | Herstellung von mit enantiomer angereicherten ortho-substituierten alpha, alpha-diaromatischen methanolen |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US5646330A (de) |
| EP (1) | EP0809626B1 (de) |
| JP (1) | JP3868488B2 (de) |
| AT (1) | ATE183995T1 (de) |
| AU (1) | AU4787696A (de) |
| CA (1) | CA2211981C (de) |
| DE (1) | DE69604054T2 (de) |
| WO (1) | WO1996025390A1 (de) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010518014A (ja) | 2007-01-31 | 2010-05-27 | バーテックス ファーマシューティカルズ インコーポレイテッド | キナーゼ阻害剤として有用な２−アミノピリジン誘導体 |
| CA2704266A1 (en) | 2007-11-02 | 2009-06-11 | Vertex Pharmaceuticals Incorporated | [1h- pyrazolo [3, 4-b] pyridine-4-yl] -phenyle or -pyridin-2-yle derivatives as protein kinase c-theta |
| EP2318407B1 (de) | 2008-07-23 | 2013-01-02 | Vertex Pharmaceuticals Incorporated | Pyrazolpyridine als kinaseinhibitoren |
| US8569337B2 (en) | 2008-07-23 | 2013-10-29 | Vertex Pharmaceuticals Incorporated | Tri-cyclic pyrazolopyridine kinase inhibitors |
| JP5631310B2 (ja) | 2008-07-23 | 2014-11-26 | バーテックス ファーマシューティカルズ インコーポレイテッドＶｅｒｔｅｘ Ｐｈａｒｍａｃｅｕｔｉｃａｌｓ Ｉｎｃｏｒｐｏｒａｔｅｄ | 三環式ピラゾロピリジンキナーゼ阻害剤 |
| CA2732765A1 (en) * | 2008-08-06 | 2010-02-11 | Vertex Pharmaceuticals Incorporated | Aminopyridine kinase inhibitors |
| WO2010129668A1 (en) | 2009-05-06 | 2010-11-11 | Vertex Pharmaceuticals Incorporated | Pyrazolopyridines |
| MX2012008643A (es) | 2010-01-27 | 2013-02-26 | Vertex Pharma | Inhibidores de cinasas de pirazolopiridinas. |
| US9067932B2 (en) | 2010-01-27 | 2015-06-30 | Vertex Pharmaceuticals Incorporated | Pyrazolopyridine kinase inhibitors |
| CN102869663A (zh) | 2010-01-27 | 2013-01-09 | 沃泰克斯药物股份有限公司 | 吡唑并吡嗪激酶抑制剂 |
| CN118772088B (zh) * | 2024-06-14 | 2025-10-03 | 北京农学院 | 2-丁烯羟酸内酯硫代乙酸酯类化合物及其制备方法和应用 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4866181A (en) * | 1986-08-29 | 1989-09-12 | Aldrich-Boranes, Inc. | Process for producing optically active alcohols |
| US5043479A (en) * | 1986-08-29 | 1991-08-27 | Aldrich Chemical Company, Inc. | Chemically and optically pure diisopinocampheylhaloboranes |
| US4772752A (en) * | 1986-08-29 | 1988-09-20 | Aldrich-Boranes, Inc. | Mono- and diisopinocampheylhaloboranes as new chiral reducing agents |
| US4950791A (en) * | 1988-03-30 | 1990-08-21 | Brown Herbert C | Novel process of producing phenyl or substituted phenylalkylamine pharmaceutical agents and novel chiral intermediates of high enantiomeric purity useful therein |
| US4868344A (en) * | 1988-03-30 | 1989-09-19 | Aldrich-Boranes, Inc. | Novel process of producing phenyl or substituted phenylalkylamine pharmaceutical agents and novel chiral intermediates of high enantiomeric purity useful therein |
| ES2108855T3 (es) * | 1992-07-21 | 1998-01-01 | Ciba Geigy Ag | Derivados de acido oxamico como agentes hipocolesteremicos. |
-
1995
- 1995-02-17 US US08/390,255 patent/US5646330A/en not_active Expired - Fee Related
-
1996
- 1996-02-06 CA CA002211981A patent/CA2211981C/en not_active Expired - Fee Related
- 1996-02-06 EP EP96903991A patent/EP0809626B1/de not_active Expired - Lifetime
- 1996-02-06 JP JP52462996A patent/JP3868488B2/ja not_active Expired - Fee Related
- 1996-02-06 AT AT96903991T patent/ATE183995T1/de not_active IP Right Cessation
- 1996-02-06 AU AU47876/96A patent/AU4787696A/en not_active Abandoned
- 1996-02-06 DE DE69604054T patent/DE69604054T2/de not_active Expired - Fee Related
- 1996-02-06 WO PCT/EP1996/000479 patent/WO1996025390A1/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| JP3868488B2 (ja) | 2007-01-17 |
| CA2211981A1 (en) | 1996-08-22 |
| DE69604054T2 (de) | 2000-01-27 |
| US5646330A (en) | 1997-07-08 |
| AU4787696A (en) | 1996-09-04 |
| EP0809626B1 (de) | 1999-09-01 |
| DE69604054D1 (de) | 1999-10-07 |
| JPH11500118A (ja) | 1999-01-06 |
| CA2211981C (en) | 2008-04-15 |
| WO1996025390A1 (en) | 1996-08-22 |
| EP0809626A1 (de) | 1997-12-03 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| RER | Ceased as to paragraph 5 lit. 3 law introducing patent treaties |