ES8600741A1 - Un procedimiento para la preparacion de nuevos derivados de isoindol - Google Patents
Un procedimiento para la preparacion de nuevos derivados de isoindolInfo
- Publication number
- ES8600741A1 ES8600741A1 ES533937A ES533937A ES8600741A1 ES 8600741 A1 ES8600741 A1 ES 8600741A1 ES 533937 A ES533937 A ES 533937A ES 533937 A ES533937 A ES 533937A ES 8600741 A1 ES8600741 A1 ES 8600741A1
- Authority
- ES
- Spain
- Prior art keywords
- preparation
- isoindole derivatives
- piperidinyl
- isoindole
- oxoisoindole
- 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
Links
- 125000000904 isoindolyl group Chemical class C=1(NC=C2C=CC=CC12)* 0.000 title 1
- 150000001875 compounds Chemical group 0.000 abstract 2
- VHMICKWLTGFITH-UHFFFAOYSA-N 2H-isoindole Chemical compound C1=CC=CC2=CNC=C21 VHMICKWLTGFITH-UHFFFAOYSA-N 0.000 abstract 1
- -1 6-chloro-2 Chemical class 0.000 abstract 1
- 230000003276 anti-hypertensive effect Effects 0.000 abstract 1
- 239000002934 diuretic Substances 0.000 abstract 1
- 230000001882 diuretic effect Effects 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical compound C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
-
- 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
- A61P7/10—Antioedematous agents; Diuretics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/08—Vasodilators for multiple indications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members 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
- C07D211/56—Nitrogen atoms
- C07D211/58—Nitrogen atoms attached in position 4
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Indole Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Suspension Of Electric Lines Or Cables (AREA)
- Liquid Developers In Electrophotography (AREA)
- Transformer Cooling (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
PROCEDIMIENTO PARA LA OBTENCION DE DERIVADOS DE ISOINDOL Y DE SUS SALES DE ADICIPN DE ACIDO FISIOLOGICAMENTE COMPATIBLES, DE FORMULA (I), EN LA QUE X ES HALOGENO O TRIFLUORMETILO; Y ES UN ENLACE SENCILLO O UN ALQUILENO DIVALENTE C1-4; Y R1 Y R2 PUEDEN SER VARIOS TIPOS DE RADICALES.CONSISTE EN LA REACCION DE UN COMPUESTOS PIPERIDINILICO DE FORMULA (II) CON UN COMPUESTO FENIALQUILICO DE FORMULA (III), EN LAS QUE Z ES UN GRUPO SALIENTE REACTIVO, Y LOS DEMAS SIMBOLOS TIENEN EL MISMO SIGNIFICADO QUE EN LA FORMULA (I). LA REACCION SE EFECTUA EN UN DISOLVENTE ORGANICO INERTE, EN PRESENCIA DE UN AGENTE DE CONDENSACION BASICO O DE UNA AMINA TERCIARIA, A TEMPERATURA ENTRE 50JC Y 200JC.ESTOS COMPUESTOS TIENEN APLICACIONES FARMACOLOGICAS POR SUS PROPIEDADES DIURETICAS Y ANTIHIPERTENSIVAS.-
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US06/441,204 US4495194A (en) | 1982-11-12 | 1982-11-12 | Antihypertensive isoindole derivatives |
Publications (2)
Publication Number | Publication Date |
---|---|
ES8600741A1 true ES8600741A1 (es) | 1985-10-16 |
ES533937A0 ES533937A0 (es) | 1985-10-16 |
Family
ID=23751955
Family Applications (5)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES527146A Expired ES8504172A1 (es) | 1982-11-12 | 1983-11-10 | Un procedimiento para la preparacion de nuevos derivados de isoindol. |
ES533938A Expired ES8600742A1 (es) | 1982-11-12 | 1984-07-02 | Un procedimiento para la preparacion de nuevos derivados de isoindol |
ES533939A Expired ES8600743A1 (es) | 1982-11-12 | 1984-07-02 | Un procedimiento de preparacion de nuevos derivados de 4-aminopiperidina |
ES533937A Granted ES533937A0 (es) | 1982-11-12 | 1984-07-02 | Un procedimiento para la preparacion de nuevos derivados de isoindol |
ES533936A Expired ES8600740A1 (es) | 1982-11-12 | 1984-07-02 | Un procedimiento para la preparacion de nuevos derivados de isoindol |
Family Applications Before (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES527146A Expired ES8504172A1 (es) | 1982-11-12 | 1983-11-10 | Un procedimiento para la preparacion de nuevos derivados de isoindol. |
ES533938A Expired ES8600742A1 (es) | 1982-11-12 | 1984-07-02 | Un procedimiento para la preparacion de nuevos derivados de isoindol |
ES533939A Expired ES8600743A1 (es) | 1982-11-12 | 1984-07-02 | Un procedimiento de preparacion de nuevos derivados de 4-aminopiperidina |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES533936A Expired ES8600740A1 (es) | 1982-11-12 | 1984-07-02 | Un procedimiento para la preparacion de nuevos derivados de isoindol |
Country Status (15)
Country | Link |
---|---|
US (1) | US4495194A (es) |
EP (1) | EP0111397B1 (es) |
JP (2) | JPS59101483A (es) |
KR (1) | KR870001168B1 (es) |
AT (1) | ATE40999T1 (es) |
AU (2) | AU566900B2 (es) |
CA (1) | CA1246081A (es) |
DE (1) | DE3379267D1 (es) |
DK (2) | DK165116C (es) |
ES (5) | ES8504172A1 (es) |
FI (1) | FI82691C (es) |
GR (1) | GR81279B (es) |
IE (1) | IE56231B1 (es) |
PT (1) | PT77651B (es) |
ZA (1) | ZA838361B (es) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU636164B2 (en) * | 1982-11-12 | 1993-04-22 | Bristol-Myers Squibb Company | 2,3-dihydro-1-hydroxy-3-oxo-2-(1-substituted-4-piperidinyl)- 1N-isoindole derivatives |
EP0351283A1 (fr) * | 1988-07-12 | 1990-01-17 | Synthelabo | Dérivés de [(pipéridinyl-4) méthyl]-2 dihydro-2,3 1H-isoindole et tétrahydro-2,3,4,5 1H-benzazépines, leur préparation et leur application en thérapeutique |
EP0497843A4 (en) * | 1989-10-27 | 1992-09-23 | The Du Pont Merck Pharmaceutical Company | (n-phthalimidoalkyl) piperidines |
US5356906A (en) * | 1989-10-27 | 1994-10-18 | The Du Pont Merck Pharmaceutical Company | (N-phthalimidoalkyl) piperidines useful as treatments for psychosis |
JP2807577B2 (ja) * | 1990-06-15 | 1998-10-08 | エーザイ株式会社 | 環状アミド誘導体 |
EP1260512B1 (en) * | 2000-02-29 | 2007-07-04 | Mitsubishi Pharma Corporation | Novel cyclic amide derivatives |
US8939859B2 (en) | 2012-10-19 | 2015-01-27 | Caterpillar Inc. | Torque converter with stator clutch |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3579524A (en) * | 1968-06-05 | 1971-05-18 | Miles Lab | 2-aminoalkyl derivatives of phthalimidines |
GB1486104A (en) * | 1975-01-23 | 1977-09-21 | Wyeth John & Brother Ltd | Phthalimidopiperidine derivatives |
IL52413A (en) * | 1977-06-29 | 1980-01-31 | Teva Pharma | Process for the preparazione of 5-chloro-6-sulfamyl-isoindolinone derivatives |
SE7907121L (sv) * | 1979-08-27 | 1981-02-28 | Astra Laekemedel Ab | Ftalimidinderivat |
-
1982
- 1982-11-12 US US06/441,204 patent/US4495194A/en not_active Expired - Fee Related
-
1983
- 1983-11-09 ZA ZA838361A patent/ZA838361B/xx unknown
- 1983-11-09 FI FI834112A patent/FI82691C/fi not_active IP Right Cessation
- 1983-11-09 GR GR72928A patent/GR81279B/el unknown
- 1983-11-09 CA CA000440844A patent/CA1246081A/en not_active Expired
- 1983-11-10 ES ES527146A patent/ES8504172A1/es not_active Expired
- 1983-11-11 EP EP83306911A patent/EP0111397B1/en not_active Expired
- 1983-11-11 DE DE8383306911T patent/DE3379267D1/de not_active Expired
- 1983-11-11 AT AT83306911T patent/ATE40999T1/de active
- 1983-11-11 DK DK517383A patent/DK165116C/da not_active IP Right Cessation
- 1983-11-11 AU AU21183/83A patent/AU566900B2/en not_active Ceased
- 1983-11-11 PT PT77651A patent/PT77651B/pt not_active IP Right Cessation
- 1983-11-11 JP JP58211113A patent/JPS59101483A/ja active Granted
- 1983-11-11 IE IE2638/83A patent/IE56231B1/en not_active IP Right Cessation
- 1983-11-12 KR KR1019830005375A patent/KR870001168B1/ko not_active IP Right Cessation
-
1984
- 1984-07-02 ES ES533938A patent/ES8600742A1/es not_active Expired
- 1984-07-02 ES ES533939A patent/ES8600743A1/es not_active Expired
- 1984-07-02 ES ES533937A patent/ES533937A0/es active Granted
- 1984-07-02 ES ES533936A patent/ES8600740A1/es not_active Expired
-
1987
- 1987-10-05 AU AU79369/87A patent/AU604756B2/en not_active Ceased
-
1990
- 1990-06-22 DK DK153690A patent/DK153690A/da not_active IP Right Cessation
-
1991
- 1991-10-30 JP JP3310030A patent/JPH051058A/ja active Granted
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FD1A | Patent lapsed |
Effective date: 19970401 |