KR910000731A - 4-아미노 3-카르복시 퀴놀린 및 나프티리딘, 그 제조방법 및 그의 의약품으로서 용도 - Google Patents

4-아미노 3-카르복시 퀴놀린 및 나프티리딘, 그 제조방법 및 그의 의약품으로서 용도 Download PDF

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KR910000731A
KR910000731A KR1019890007791A KR890007791A KR910000731A KR 910000731 A KR910000731 A KR 910000731A KR 1019890007791 A KR1019890007791 A KR 1019890007791A KR 890007791 A KR890007791 A KR 890007791A KR 910000731 A KR910000731 A KR 910000731A
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alkyl
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hydrogen
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phenyl
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멍데 에띠앙
베르니에르 쟝-끌로드
위젠스 끼안 뻬떼르
바씨 앙드레
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미쉘 드 아스
사노피 쏘시에떼 아노님
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Priority claimed from FR8807498A external-priority patent/FR2632305B1/fr
Priority claimed from FR8808025A external-priority patent/FR2632861B1/fr
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Publication of KR910000731A publication Critical patent/KR910000731A/ko

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Abstract

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Description

4-아미노3-카르복시 퀴놀린 및 나프티리딘, 그 제조방법 및 그의 의약품으로서 용도
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (22)

  1. 라세미체 또는 거울상 이성질체 형태의 식(Ⅰ)의 화합물 및 그의 약학적으로 허용될 수 있는 산 또는 염기부가염.
    위 식에서, R1과 R2는 같거나 다르며 각기 수소, C1-C6의 알킬, C2-C6의 알킬렌, 페닐, 벤질중의 하나이거나, R1과 R2는 그들이 결합된 질소와 함께 C4-C8의 포화헤테로사이클을 형성하고, R3는 수소, C1-C6의 알킬, 페닐 또는 C7-C9의 페닐알킬중의 하나이고, R4는 수소 또는 C1-C4의 알킬중의 하나이고 R5와 R6는 같거나 다르며 각기 수소, 할로겐, C1-C3의 알킬 또는 알콕시, 니트로 또는 트리플루오로메틸 중의 하나이거나 같이 메틸렌디옥시그룹을 형성하고, Z는 R7이 수소 또는 C1-C6의 알킬중의 하나인 OR7이거나; R8과 R9가 각기 수소, C1-C4의 알킬, 페닐, 벤질중의 하나인 NR8R9이거나; C1-C4의 알킬이거나; 벤질이거나; 헤테로원자가 있거나 또는 없는 C4-C6의 아릴이고, R10은 Z가 벤질 또는 페닐이 아니고 R3가 수소가 아니고, 페닐 및 벤질 그룹이 할로겐, C1-C3의 알콕시, 알킬 또는 티오알킬, 니트로, 트리플루오로 메틸 또는 하이드록시로 치환될 수 있고, 알킬 및 알콕시 그룹이 직쇄, 분지 또는 고리모양이라는 조건하에 수소, C1-C4의 알킬 또는 페닐 중의 하나이다. n은 0,1 또는 2이고, p는 0또는 1이며, A, B, C, D의 하나는 N이고 나머지 CH이거나, A, B, C, D 모두는 각기 CH를 나타낸다.
  2. 제1항에 있어서, Z가 치환 또는 미치환된 페닐그룹인 것을 특징으로 하는 식Ⅰ의 화합물.
  3. 제2항에 있어서, Z가 미치환된 페닐그룹인 것을 특징으로 하는 화합물.
  4. 제1항에 있어서, Z가 피리딜, 피롤릴, 푸릴, 티에닐 또는 이미다졸릴인 것을 특징으로 하는 식Ⅰ의 화합물.
  5. 제1항에 있어서, Z가 OR7인 것을 특징으로 하는 식Ⅰ의 화합물.
  6. 제5항에 있어서, R7이 알킬인 것을 특징으로 하는 화합물.
  7. 제5항에 있어서, Z가 C1-C3의 알킬인 것을 특징으로 하는 화합물.
  8. 제1항 내지 제7항 중 어느 한 항에 있어서, A, B, C, D가 각기 CH인 것을 특징으로 하는 식Ⅰ의 화합물.
  9. 제1항 내지 제7항 중 어느 한항에 있어서, A, B, C 또는 D중 어느 하나가 N인 것을 특징으로 하는 식Ⅰ의 화합물.
  10. 제9항에 있어서, A가 N인 것을 특징으로 하는 화합물.
  11. 제1항에 있어서, R1과 R2가 각기 의 C1-C6알킬이고, R3이 C1-C3의 알킬이고, R10이 수소이고, Z가 R7이 C1-C6의 알킬인 OR7인 것을 특징으로 하는 식Ⅰ의 화합물.
  12. 제11항에 있어서, R4가 수소인 것을 특징으로 하는 화합물.
  13. 제11항에 있어서, R4가 수소이고, C가 치환된 것을 특징으로 하는 화합물.
  14. 제1항에 있어서, R1가 알킬이고, R2및 Z가 각기 치환될 수 있는 페닐인 것을 특징으로 하는 식Ⅰ의 화합물.
  15. 제1항에 있어서, R1가 알킬이고, R2및 Z가 치환될 수 있는 페닐이고, R3과 R10이 각기 수소인 것을 특징으로 하는 식Ⅰ의 화합물.
  16. 제14항과 제15항중 어느 한항에 있어서, A, B, C, D가 각기 CH인 것을 특징으로 하는 화합물.
  17. 제14항과 제15항중 어느 한항에 있어서, A가 N이고 B, C 및 D가 CH인 것을 특징으로 하는 화합물.
  18. 에틸7-클로로4-(1-N,N-디프로필카르바모일)에틸 아미노 퀴놀린3-카르복시레이트 및 그의 약학적으로 허용할 수 있는 산부가염.
  19. 3-벤조일7-클로로4-(N-메틸N-4-클로로페닐)카르바모일 메틸아미노 퀴놀린 및 그의 약학적으로 허용될 수 있는 산부가염.
  20. 3-벤조일4-(N-메틸N-4-클로로페닐)카르바모일 메틸아미노 1,5-나프티리딘 및 그의 약학적으로 허용될 수 있는 산부가염.
  21. 식Ⅱ의 아민과 식Ⅲ의 화합물을 반응시키는 것을 특징으로 하는 식Ⅰ의 화합물을 제조하는 방법.
    위 식에서 R1, R2, R3, R4, R5, R6, R10, Z, A, B, C, D, n 및 p는 제1항과 같은 의미이고 X는 할로겐 또는 설포네이트 중의 하나이다.
  22. 양립할 수 있는 부형제 뿐만 아니라 제1항 내지 제20항중 어는 한 항에 의한 화합물을 유효성분으로 함유하는 약학적인 조성물.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019890007791A 1988-06-06 1989-06-05 4-아미노 3-카르복시 퀴놀린 및 나프티리딘, 그 제조방법 및 그의 의약품으로서 용도 KR910000731A (ko)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
FR8807498A FR2632305B1 (fr) 1988-06-06 1988-06-06 Amino-4 aroyl-3 quinoleines et naphtyridines, leur procede de preparation et leur application en therapeutique
FR88-07498 1988-06-06
FR88-08025 1988-06-15
FR8808025A FR2632861B1 (fr) 1988-06-15 1988-06-15 Derives d'amino-4 carboxy-3 quinoleines et naphtyridines, leur procede de preparation et leur application comme medicaments

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KR910000731A true KR910000731A (ko) 1991-01-30

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US (1) US5026711A (ko)
EP (1) EP0346208B1 (ko)
JP (1) JP2766672B2 (ko)
KR (1) KR910000731A (ko)
AU (1) AU624825B2 (ko)
CA (1) CA1337073C (ko)
DE (1) DE68914515T2 (ko)
DK (1) DK273689A (ko)
ES (1) ES2063153T3 (ko)
IE (1) IE63429B1 (ko)
NZ (1) NZ229413A (ko)
PT (1) PT90748B (ko)

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FR2581382B1 (fr) * 1985-05-06 1987-06-26 Sanofi Sa Derives n-(quinolyl) glycinamides, leur procede de preparation et leur application therapeutique en tant que psychotropes
GB8610981D0 (en) * 1986-05-06 1986-06-11 Ici America Inc Quinoline amides
GB8621425D0 (en) * 1986-09-05 1986-10-15 Smith Kline French Lab Compounds
US5034393A (en) * 1989-07-27 1991-07-23 Dowelanco Fungicidal use of pyridopyrimidine, pteridine, pyrimidopyrimidine, pyrimidopyridazine, and pyrimido-1,2,4-triazine derivatives
AU634561B2 (en) * 1989-07-27 1993-02-25 Eli Lilly And Company Naphthyridine derivatives

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ES2063153T3 (es) 1995-01-01
PT90748A (pt) 1989-12-29
EP0346208A1 (fr) 1989-12-13
DK273689D0 (da) 1989-06-02
AU624825B2 (en) 1992-06-25
DE68914515T2 (de) 1994-08-18
JPH0232058A (ja) 1990-02-01
EP0346208B1 (fr) 1994-04-13
IE891797L (en) 1989-12-06
US5026711A (en) 1991-06-25
DE68914515D1 (de) 1994-05-19
CA1337073C (en) 1995-09-19
NZ229413A (en) 1990-11-27
PT90748B (pt) 1994-10-31
AU3603589A (en) 1989-12-07
DK273689A (da) 1989-12-07
JP2766672B2 (ja) 1998-06-18
IE63429B1 (en) 1995-04-19

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