ES2098786T3 - Nuevas benzopiranonas, procedimientos para su preparacion y utilizacion. - Google Patents
Nuevas benzopiranonas, procedimientos para su preparacion y utilizacion.Info
- Publication number
- ES2098786T3 ES2098786T3 ES93921925T ES93921925T ES2098786T3 ES 2098786 T3 ES2098786 T3 ES 2098786T3 ES 93921925 T ES93921925 T ES 93921925T ES 93921925 T ES93921925 T ES 93921925T ES 2098786 T3 ES2098786 T3 ES 2098786T3
- Authority
- ES
- Spain
- Prior art keywords
- group
- atoms
- alkyl
- pct
- groups
- 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
- C07D311/06—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 2
- C07D311/08—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 2 not hydrogenated in the hetero ring
- C07D311/16—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 2 not hydrogenated in the hetero ring substituted in position 7
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/08—Antiepileptics; Anticonvulsants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/22—Anxiolytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/26—Psychostimulants, e.g. nicotine, cocaine
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
SE DESCRIBEN 2H - 1 - BENZOPIRANO - 2 - ONAS (DERIVADOS CUMARINA) DE LA FORMULA GENERAL I DONDE R1 SIGNIFICA UN RESTO HIDROXI, UN RESTO ALCOXI INFERIOR, UN RESTO CICLOALCOXI CON 4 HASTA 6 ATOMOS DE C O UN RESTO ALQUIL O RESTO ARILSULFONIL, R6 SO2O -, R2 Y R3 DE FORMA INDEPENDIENTE UNO DE OTRO SIGNIFICAN UN ATOMO DE HIDROGENO, RESTO HIDROXI, RESTO ALCOXI INFERIOR O RESTO CICLOALCOXI CON 4 HASTA 6 ATOMOS DE C, R4 ES UN ATOMO DE HIDROGENO, UN GRUPO ALQUIL INFERIOR CON 1 HASTA 4 ATOMOS DE C O UN RESTO FENIL, Y ES UN ATOMO DE NITROGENO, UN GRUPO CH O UN GRUPO COH, R5 ES UN RESTO FENIL, NAFTIL, PIRIDINIL O RESTO RIPIMIDINIL, QUE EVENTUALMENTE ES SUSTITUIDO DE FORMA RESPECTIVA CON 1 O 2 GRUPOS C1 - C15 - ALQUIL, RESPECTIVAMENTE CON 1 O 2 ATOMOS DE HALOGENO, CON HALOGENO Y AL MISMO TIEMPO C1- C5 ALQUIL, CON PERFLUOR ALQUIL CON 1 HASTA 3 ATOMOS DE C, C1 - C5 ALCOXI, HIDROXI, METILENDIOXI O NITRO, R6 ES UN RESTO ALQUIL INFERIOR, UN RESTO CICLOALQUIL CON 4 HASTA 6 ATOMOS DE C O UN RESTO FENIL, QUE EVENTUALMENTE ES SUSTITUIDO DE FORMA RESPECTIVA CON 1 O 2 GRUPOS C1 - C5 - ALQUIL, CON 1 O 2 ATOMOS DE HALOGENO O CON PERFLUOR ALQUIL CON 1 HASTA 3 ATOMOS DE C, Y N = 1 HASTA 4, ASI COMO SUS COMPUESTOS DE ADICION CON ACIDOS TOLERABLES FISIOLOGICAMENTE. SE DESCRIBEN ADEMAS PROCESOS PARA LA ELABORACION DE ESTOS COMPUESTOS ASI COMO NUEVOS PRODUCTOS INTERMEDIOS Y PROCESOS PARA SU ELABORACION. LOS NUEVOS DERIVADOS CUMARINA POSEEN ACTIVIDAD NEUROPROTECTIVA Y SICOFARMACOLOGICA. LOS MEDICAMENTOS QUE CONTIENEN ESTOS COMPUESTOS SON EVENTUALMENTE OBJETO DE LA INVENCION.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE4233963A DE4233963A1 (de) | 1992-10-08 | 1992-10-08 | Neue Benzopyranone, Verfahren zu ihrer Herstellung und Verwendung |
Publications (1)
Publication Number | Publication Date |
---|---|
ES2098786T3 true ES2098786T3 (es) | 1997-05-01 |
Family
ID=6470008
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES93921925T Expired - Lifetime ES2098786T3 (es) | 1992-10-08 | 1993-10-06 | Nuevas benzopiranonas, procedimientos para su preparacion y utilizacion. |
Country Status (9)
Country | Link |
---|---|
US (1) | US5550129A (es) |
EP (1) | EP0663911B1 (es) |
JP (1) | JP3575610B2 (es) |
AT (1) | ATE148697T1 (es) |
AU (1) | AU674167B2 (es) |
CA (1) | CA2146646C (es) |
DE (2) | DE4233963A1 (es) |
ES (1) | ES2098786T3 (es) |
WO (1) | WO1994008985A1 (es) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2724656B1 (fr) * | 1994-09-15 | 1996-12-13 | Adir | Nouveaux derives du benzopyranne, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
US5922719A (en) * | 1997-08-11 | 1999-07-13 | Warner-Lambert Company | Coumarin dopamine D4 receptor antagonists |
IL124195A (en) * | 1998-04-23 | 2000-08-31 | Chemagis Ltd | Process for the preparation of esters of 2-¬4-¬4-chlorophenyl¾phenylmethyl¾-1-piperazinyl¬ethoxy¾acetic acid |
US6177566B1 (en) | 1998-06-30 | 2001-01-23 | Neurogen Corporation | 6-(4-arylalkylpiperazin-1-yl) benzodioxane and 6-(4-arylalkylpiperazin-1-yl) chromane derivatives: dopamine receptor subtype specific ligands |
WO2000000489A2 (en) * | 1998-06-30 | 2000-01-06 | Neurogen Corporation | 6-(4-arylalkylpiperazin-1-yl)benzodioxane and 6-(4-arylalkylpiperazin-1-yl)chromane derivatives: dopamine receptor subtype specific ligands |
AR059339A1 (es) * | 2006-02-09 | 2008-03-26 | Chugai Pharmaceutical Co Ltd | Derivados de la cumarina para trastornos proliferativos de celulas, composicion farmaceutica y agente terapeutico que los contiene |
WO2009014100A1 (ja) * | 2007-07-20 | 2009-01-29 | Chugai Seiyaku Kabushiki Kaisha | p27蛋白質誘導剤 |
FR2949465B1 (fr) * | 2009-09-01 | 2011-08-12 | Pf Medicament | Derives chromones, leur procede de preparation et leurs applications therapeutiques |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3538098A (en) * | 1966-11-02 | 1970-11-03 | Cassella Farbwerke Mainkur Ag | Process for the production of coumarin derivatives |
DE1670468A1 (de) * | 1966-11-02 | 1971-03-18 | Cassella Farbwerke Mainkur Ag | Verfahren zur Herstellung von Derivaten des Cumarins |
US3930003A (en) * | 1970-07-17 | 1975-12-30 | Troponwerke Dinklage & Co | Coumarine derivatives and process for the preparation thereof |
DE2108185A1 (en) * | 1971-02-20 | 1972-09-07 | Troponwerke Dinklage & Co, 5000 Köln-Mülheim | N-(3-aminoalkyl-2-oxo-2h-1-benzopyran-7-yl) ureas - as coronary vasodilators |
DE2448257A1 (de) * | 1974-10-10 | 1976-04-22 | Troponwerke Dinklage & Co | Cumarinabkoemmlinge, verfahren zu ihrer herstellung sowie ihre verwendung als arzneimittel |
-
1992
- 1992-10-08 DE DE4233963A patent/DE4233963A1/de not_active Withdrawn
-
1993
- 1993-10-06 ES ES93921925T patent/ES2098786T3/es not_active Expired - Lifetime
- 1993-10-06 DE DE59305415T patent/DE59305415D1/de not_active Expired - Fee Related
- 1993-10-06 JP JP50958194A patent/JP3575610B2/ja not_active Expired - Fee Related
- 1993-10-06 US US08/411,621 patent/US5550129A/en not_active Expired - Fee Related
- 1993-10-06 CA CA002146646A patent/CA2146646C/en not_active Expired - Fee Related
- 1993-10-06 WO PCT/EP1993/002742 patent/WO1994008985A1/de active IP Right Grant
- 1993-10-06 EP EP93921925A patent/EP0663911B1/de not_active Expired - Lifetime
- 1993-10-06 AU AU51113/93A patent/AU674167B2/en not_active Ceased
- 1993-10-06 AT AT93921925T patent/ATE148697T1/de not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
CA2146646C (en) | 2004-06-01 |
JPH08502269A (ja) | 1996-03-12 |
EP0663911B1 (de) | 1997-02-05 |
AU5111393A (en) | 1994-05-09 |
WO1994008985A1 (de) | 1994-04-28 |
DE4233963A1 (de) | 1994-04-14 |
US5550129A (en) | 1996-08-27 |
AU674167B2 (en) | 1996-12-12 |
CA2146646A1 (en) | 1994-04-28 |
EP0663911A1 (de) | 1995-07-26 |
ATE148697T1 (de) | 1997-02-15 |
JP3575610B2 (ja) | 2004-10-13 |
DE59305415D1 (de) | 1997-03-20 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FG2A | Definitive protection |
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