ES2188222T3 - Sintesis enantioselectiva. - Google Patents
Sintesis enantioselectiva.Info
- Publication number
- ES2188222T3 ES2188222T3 ES99940813T ES99940813T ES2188222T3 ES 2188222 T3 ES2188222 T3 ES 2188222T3 ES 99940813 T ES99940813 T ES 99940813T ES 99940813 T ES99940813 T ES 99940813T ES 2188222 T3 ES2188222 T3 ES 2188222T3
- Authority
- ES
- Spain
- Prior art keywords
- enantioselective synthesis
- xiv
- formula
- pharmaceutically acceptable
- acceptable salt
- 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.)
- Expired - Lifetime
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
- C07D311/22—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 4
- C07D311/26—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 4 with aromatic rings attached in position 2 or 3
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/24—Drugs for disorders of the endocrine system of the sex hormones
- A61P5/32—Antioestrogens
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
- C07D311/58—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4
- C07D311/60—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4 with aryl radicals attached in position 2
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Diabetes (AREA)
- Endocrinology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyrane Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
- Steroid Compounds (AREA)
- Hydrogenated Pyridines (AREA)
Abstract
Un procedimiento de hacer reaccionar el compuesto de fórmula IV con el compuesto representado por la fórmula VII para producir el compuesto de fórmula IX, caracterizado porque el compuesto de fórmula IV se hace reaccionar con el compuesto representado por la fórmula VII **(Fórmula)** en presencia de piperidina, una base de amina orgánica impedida y un alcanol de C3-C6 a temperatura y durante un tiempo suficiente para producir el compuesto de fórmula IX químicamente puro y libre del isómero cis del compuesto de fórmula IX y libre de las chalconas E y Z de fórmula VIII, en el que HPG es un grupo protector de hidroxilo fenólico lábil frente a ácidos: **(Fórmula)**
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US13421698A | 1998-08-14 | 1998-08-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2188222T3 true ES2188222T3 (es) | 2003-06-16 |
Family
ID=22462296
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES99940813T Expired - Lifetime ES2188222T3 (es) | 1998-08-14 | 1999-08-12 | Sintesis enantioselectiva. |
Country Status (10)
| Country | Link |
|---|---|
| EP (1) | EP1104414B1 (es) |
| JP (2) | JP3684332B2 (es) |
| CN (1) | CN1146554C (es) |
| AT (1) | ATE232525T1 (es) |
| AU (1) | AU5459399A (es) |
| CA (1) | CA2340343C (es) |
| DE (1) | DE69905376T2 (es) |
| ES (1) | ES2188222T3 (es) |
| WO (1) | WO2000009493A1 (es) |
| ZA (1) | ZA200100875B (es) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| HUE033581T2 (hu) | 2010-06-10 | 2017-12-28 | Seragon Pharmaceuticals Inc | Ösztrogén receptor modulátorok és alkalmazásaik |
| JP6112625B2 (ja) | 2011-12-14 | 2017-04-12 | セラゴン ファーマシューティカルズ,インク. | フッ素化したエストロゲン受容体モジュレーターおよびその使用 |
| PE20150099A1 (es) | 2011-12-16 | 2015-01-30 | Olema Pharmaceuticals Inc | Compuestos novedosos de benzopirano, composiciones y usos de los mismos |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5395842A (en) * | 1988-10-31 | 1995-03-07 | Endorecherche Inc. | Anti-estrogenic compounds and compositions |
| US5254568A (en) * | 1990-08-09 | 1993-10-19 | Council Of Scientific & Industrial Research | Benzopyrans as antiestrogenic agents |
| US6060503A (en) * | 1991-12-02 | 2000-05-09 | Endorecherche, Inc. | Benzopyran-containing compounds and method for their use |
| US5407947A (en) * | 1993-11-05 | 1995-04-18 | Eli Lilly And Company | Methods for inhibiting bone loss using pyrolidine and piperidine substituted benzopyrans |
| WO1999002513A1 (en) * | 1997-07-09 | 1999-01-21 | Novo Nordisk A/S | Preparation of diaryl-benzopyrans |
| AU8102398A (en) * | 1997-07-09 | 1999-02-08 | Central Drug Research Institute | (dl)-2,3-diaryl-2h-1-benzopyrans |
| US6465445B1 (en) * | 1998-06-11 | 2002-10-15 | Endorecherche, Inc. | Medical uses of a selective estrogen receptor modulator in combination with sex steroid precursors |
-
1999
- 1999-08-12 DE DE69905376T patent/DE69905376T2/de not_active Expired - Lifetime
- 1999-08-12 CA CA002340343A patent/CA2340343C/en not_active Expired - Fee Related
- 1999-08-12 AT AT99940813T patent/ATE232525T1/de not_active IP Right Cessation
- 1999-08-12 JP JP2000564945A patent/JP3684332B2/ja not_active Expired - Fee Related
- 1999-08-12 WO PCT/US1999/016711 patent/WO2000009493A1/en not_active Ceased
- 1999-08-12 CN CNB998119113A patent/CN1146554C/zh not_active Expired - Fee Related
- 1999-08-12 ES ES99940813T patent/ES2188222T3/es not_active Expired - Lifetime
- 1999-08-12 EP EP99940813A patent/EP1104414B1/en not_active Expired - Lifetime
- 1999-08-12 AU AU54593/99A patent/AU5459399A/en not_active Abandoned
-
2001
- 2001-01-31 ZA ZA2001/00875A patent/ZA200100875B/en unknown
-
2005
- 2005-04-08 JP JP2005112900A patent/JP4461048B2/ja not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JP2005206610A (ja) | 2005-08-04 |
| ATE232525T1 (de) | 2003-02-15 |
| HK1036978A1 (en) | 2002-01-25 |
| ZA200100875B (en) | 2002-06-26 |
| DE69905376D1 (de) | 2003-03-20 |
| JP4461048B2 (ja) | 2010-05-12 |
| EP1104414B1 (en) | 2003-02-12 |
| WO2000009493A1 (en) | 2000-02-24 |
| JP3684332B2 (ja) | 2005-08-17 |
| AU5459399A (en) | 2000-03-06 |
| JP2002522533A (ja) | 2002-07-23 |
| CN1322200A (zh) | 2001-11-14 |
| CA2340343A1 (en) | 2000-02-24 |
| CA2340343C (en) | 2007-04-24 |
| DE69905376T2 (de) | 2003-10-09 |
| EP1104414A1 (en) | 2001-06-06 |
| CN1146554C (zh) | 2004-04-21 |
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