KR920021546A - 알도스 환원효소 억제제로서 유용한 스피로[이소퀴놀린-4(1h), 3'-피롤리딘]-1,2',3,5'(2h)-테트론 화합물의 제조방법 및 중간체 - Google Patents
알도스 환원효소 억제제로서 유용한 스피로[이소퀴놀린-4(1h), 3'-피롤리딘]-1,2',3,5'(2h)-테트론 화합물의 제조방법 및 중간체 Download PDFInfo
- Publication number
- KR920021546A KR920021546A KR1019920008335A KR920008335A KR920021546A KR 920021546 A KR920021546 A KR 920021546A KR 1019920008335 A KR1019920008335 A KR 1019920008335A KR 920008335 A KR920008335 A KR 920008335A KR 920021546 A KR920021546 A KR 920021546A
- Authority
- KR
- South Korea
- Prior art keywords
- compound
- formula
- isoquinoline
- spiro
- pyrrolidine
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/10—Spiro-condensed systems
-
- 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
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/76—Esters of carboxylic acids having a carboxyl group bound to a carbon atom of a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/22—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems 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 carbon atoms of the nitrogen-containing ring
- C07D217/26—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
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)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (2)
- a) 일반식(II)의 화합물의 촉매량의 CuBr의 존재하에 디메틸 말로네이트 및 NaH와 반응시켜 일반식(III)의 화합물을 생성시키고, b) 일반식(III)의 화합물을 SOCl2와 반응시킨 다음 Et3N의 존재하에 통상적인 용매 속에서 R2NH2로 처리하여 일반식(IV)의 화합물을 생성시키고, c) 일반식(IV)의 화합물을 K2CO3의 존재하에 통상적인 용매 속에서 브로모아세토니트릴과 반응시켜 일반식(V)의 화합물을 생성시키고, d) 일반식(V)의 화합물의 메탄올 및 디에틸 에테르중의 무수 HCl 가스와 반응시켜 일반식(VI)의 화합물을 생성시키고, e) 일반식(VI)의 화합물을 통상적인 용매중의 염기와 반응시켜 일반식(I)의 화합물을 제조함을 특징으로 하는, 일반식(I)의 화합물의 제조방법.상기식에서, R1은 수소 또는 할로겐이고 R2는 디할로겐 치환된 벤질 또는 메틸이다.
- 일반식(V)의 화합물.상기식에서, R1은 수소 또는 할로겐이고, R2는 디할로겐 치환된 벤질 또는 메틸이다.※ 참고사항:최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US07/703,969 US5106978A (en) | 1991-05-22 | 1991-05-22 | Process and intermediates for the preparation of spiro(isoquinoline-4(1H), 3'-pyrrolidine)-1,2', 3,5'(2H)-tetrones which are useful as aldose reductase inhibitors |
US7/703969 | 1991-05-22 | ||
US07/703969 | 1991-05-22 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR920021546A true KR920021546A (ko) | 1992-12-18 |
KR100217214B1 KR100217214B1 (ko) | 1999-09-01 |
Family
ID=24827531
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019920008335A KR100217214B1 (ko) | 1991-05-22 | 1992-05-18 | 알도스 환원효소 억제제로서 유용한 스피로[이소퀴놀린-4(1h),3'-피롤리딘]-1,2',3,5'(2h)-테트론 화합물의 제조방법 및 이의 중간체 |
Country Status (6)
Country | Link |
---|---|
US (1) | US5106978A (ko) |
JP (1) | JP3474588B2 (ko) |
KR (1) | KR100217214B1 (ko) |
CA (1) | CA2068590C (ko) |
CZ (1) | CZ281171B6 (ko) |
ZA (1) | ZA923567B (ko) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2103890T3 (es) * | 1991-05-22 | 1997-10-01 | American Home Prod | Procedimiento y producto intermedio para producir derivados de isoquinoleina. |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4419517A (en) | 1973-06-01 | 1983-12-06 | E. I. Du Pont De Nemours & Co. | 4a-Aryl-trans-decahydroisoquinolines |
DE3262294D1 (en) * | 1981-05-13 | 1985-03-28 | Ici Plc | Pharmaceutical compositions containing spiro succinimide derivatives |
IE883159L (en) * | 1988-10-19 | 1990-04-19 | Hydam Ltd | Wave powered prime mover |
US4927831A (en) * | 1988-10-20 | 1990-05-22 | American Home Products | Spiro-isoquinoline-pyrrolidine tetrones and analogs thereof useful as aldose reductase inhibitors |
US5037831A (en) * | 1990-05-21 | 1991-08-06 | American Home Products Corporation | Spiro-isoquinoline-pyrrolidines and analogs thereof useful as aldose reductase inhibitors |
-
1991
- 1991-05-22 US US07/703,969 patent/US5106978A/en not_active Expired - Lifetime
-
1992
- 1992-05-14 CZ CS921458A patent/CZ281171B6/cs not_active IP Right Cessation
- 1992-05-15 CA CA002068590A patent/CA2068590C/en not_active Expired - Fee Related
- 1992-05-15 ZA ZA923567A patent/ZA923567B/xx unknown
- 1992-05-18 KR KR1019920008335A patent/KR100217214B1/ko not_active IP Right Cessation
- 1992-05-18 JP JP12461292A patent/JP3474588B2/ja not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
CZ281171B6 (cs) | 1996-07-17 |
ZA923567B (en) | 1993-11-15 |
CA2068590C (en) | 2001-12-25 |
CA2068590A1 (en) | 1992-11-23 |
KR100217214B1 (ko) | 1999-09-01 |
JPH05148264A (ja) | 1993-06-15 |
US5106978A (en) | 1992-04-21 |
JP3474588B2 (ja) | 2003-12-08 |
CS145892A3 (en) | 1992-12-16 |
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