KR890012990A - 삼치환된 아민 이들의 제법 및 이들을 함유하는 제약조성물 - Google Patents

삼치환된 아민 이들의 제법 및 이들을 함유하는 제약조성물 Download PDF

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KR890012990A
KR890012990A KR1019890002324A KR890002324A KR890012990A KR 890012990 A KR890012990 A KR 890012990A KR 1019890002324 A KR1019890002324 A KR 1019890002324A KR 890002324 A KR890002324 A KR 890002324A KR 890012990 A KR890012990 A KR 890012990A
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unsubstituted
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hydrogen atom
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차클라키디스 크리스토스
라인네르트 헤르베르트
프로인트 페터
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다움, 포우퀘트
뵈링거 만하임 게엠베하
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Publication of KR890012990A publication Critical patent/KR890012990A/ko

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Abstract

내용 없음.

Description

삼치환된 아민 이들의 제법 및 이들을 함유하는 제약조성물
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (8)

  1. 다음 일반식(Ⅰ)을 가지는 화합물 및 이들의 약리적 수용가능염 및 광학이성질체;상기식에서 R1은 수소원자, 직쇄 또는 측쇄의 C1-C12-알킬기, C3-C7-시클로알킬기, 직쇄 또는 측쇄의 C2-C12-알켄일기 또는 치환 또는 비치환된 C3-C7-모노- 또는 비시클로알켄일기, 비치환 또는 단일 또는다중치환된 모노시클릭 아로마틱 또는 헤테로아로마틱기이고, 같거나 다를 수 있는 R2및 R3은 직쇄, 측쇄, 포화 또는 불포화된 C1-C6지방족기이거나 또는, 이들의 부착되는 질소원자와 함께, 또다른 헤테로원자를 함유할 수 있으며 임의로 저급의 알킬기, 저급의 알콕시기 또는 산소원자에 의해 치환될 수 있는 포화 또는 불포화고리를 형성하며, R4는 비치환 또는 단일 또는 다중치환된 모노시클릭 아로마틱기 치환 또는 비치환된 5- 또는 6-헤테로아로마틱고리이고, R5는 수소원자, 시아노기, -CO-OR7기, 비치환 또는 단일 또는 다중치환된 모노시클릭아로마틱기 또는 치환 또는 비치환된 5- 또는 6-원 고리이며, R6은 수소원자, 시아노그룹 또는 -CO-OR7,또는 -CH2-O-R10기이며, R7은 수소원자, C1-C12-알킬기 또는 N-디알킬아미노-C1-C6-알킬기이고, 같거나 다룰 수 있는 R8및 R9는 수소원자 또는 직쇄, 측쇄, 포화 또는 불포화된 지방족 C1-C12-지방족기이거나 또는, 이들이 부착되는 질소원자와 함께, C2-C6을 가지는 포화 또는 불포화 고리를 형성하여, R10은 수소원자, 직쇄 또는 측쇄의 C1-C6-알킬 또는 C2-C6-알켄일기, 아랄킬기 또는 아실기이며, X는 원자가 결합 또는 메틸렌기이며, Y는 원자가 결합 또는 C6이하를 함유하는 직쇄, 측쇄, 포화 또는 불포화 탄화수소기이며 Z는 원자가결합, 또는 산소원자 또는 카보닐그룹이다.
  2. 제1항에 있어서, R1이 이소부틸, 메타알릴, 이소펜텐일, 푸릴, 티엔일, 피리딜 또는 페닐기이거나 또는 메틸, 메톡시 또는 할로겐에 의해 치환된 페닐기이고, R2및 R3은 둘다 에틸기이거나 또는, 이들이 부착되는 질소원자와 함께, 피롤리딘, 피페리딘 또는 모폴린고리를 형성하고, R4는 푸릴, 티엔일, 피리딜 또는 페닐기이거나 또는 메틸, 메톡시 또는 할로겐에 의해 치환된 페닐기이고, R5는 수소원자, 시나노그룹 또는 에톡시카보닐, 푸릴, 티엔일 피리딜 또는 페닐기이거나 또는 메틸, 메틸렌디옥시, 메톡시 또는 할로겐이고, R6은 수소원자, 시아노그룹 또는 메톡시카보닐, 에톡시카보닐, n-프로폭시카보닐, 이소프로폭시카보닐, 아미노카보닐, 디에틸에미노카보닐, 디메틸아미노에톡시카보닐, 피페리디노카복실 또는 히드록시메틸기이고, X는 원자가 결합이거나 또는 메틸렌기이고, Y는 원자가 결합 또는 메틸렌 또는 에틸렌기이고 Z는 원자가 결합, 산소원자 또는 카보닐그룹인 화합물 및 이들의 약리적 수용가능염 및 광학이성질체.
  3. 상기에서 특히 예시한 제1항에 따른 화합물.
  4. 공지의 방법에 의해, (a) 일반식(Ⅱ)의 화합물을 일반식(Ⅲ)의 화합물과 반응시키거나 또는, (b) 일반식(Ⅳ)의 화합물을 일반식(Ⅲ)의 화합물과 반응시켜 일반식(Ⅰ)의 화합물을 제조하고, 그 다음에 만약 필요하다면, 얻어진 일반식(Ⅰ)의 다른 화합물로 전환시키고 얻어진 화합물을 약리적 수용가능염으로 전환시키거나 또는 이들의 광학이성질체를 분리하는 방법:
    상기식에서 R1은 수소원자, 직쇄 또는 측쇄의 C1-C12-알킬기, C3-C7-시클로알킬기, 직쇄 또는 측쇄의 C2-C12-알켄일기 또는 치환 또는 비치환된 C3-C7-모노- 또는 비시클로알켄일기, 비치환 또는 단일 또는 다중치환된 모노시클릭아로마틱 또는 헤테로아로마틱기이고, 같거나 다를 수 있는 R2및 R3은 직쇄, 측쇄, 포화 또는 불포화된 C1-C6지방족기이거나 또는 이들의 부착되는 질소원자와 함께, 또다른 헤테로원자를 함유할 수 있으며 임의로 저급의 알킬기, 저급의 알콕시기 또는 산소원자에 의해 치환될 수 있는 포화 또는 불포화고리를 형성하며, R4는 비치환 또는 단일 또는 다중치환된 모노시클릭아로마틱기 치환 또는 비치환된 5- 또는 6-헤테로아로마틱고리이고, R5는 수소원자, 시아노기, -CO-OR7기, 비치환 또는 단일 또는 다중 치환된 모노시클릭아로마틱기 또는 치환 또는 비치환된 5- 또는 6-원 고리이며, R6는 수소원자, 시아노그룹 또는 -CO-OR7,또는 -CH2-O-R10기이며, R7은 수소원자, C1-C12-알킬기 또는 N-디알킬아미노-C1-C6-알킬기이고, 같거나 다룰 수 있는 R8및 R9는 수소원자 또는 직쇄, 측쇄, 포화 또는 불포화된 지방족 C1-C12-지방족기이거나 또는, 이들이 부착되는 질소원자와 함께, C2-C6을 가지는 포화 또는 불포화 고리를 형성하며, R10은 수소원자, 직쇄 또는 측쇄의 C1-C6-알킬 또는 C2-C6-알켄일기, 아랄킬기 또는 아실기이며, X는 원자가 결합 또는 메틸렌기이며, Y는 원자가 결합 또는 C6이하를 함유하는 직쇄, 측쇄, 포화 또는 불포화 탄화수소기이며 Z는 원자가결합, 또는 산소원자 또는 카보닐그룹이다.
  5. 제4항에 있어서, 상기에서 특히 예시한 제1항에 따르는 화합물의 제조방법.
  6. 제1항에 있어서, 제4 또는 5항에 따르는 방법에 의해 언제나 제조되는 화합물.
  7. 제1 내지 3항 및 6항의 어느 항에 따른 적어도 하나의 화합물 뿐 아니라 종래답체 및 보조물질을 함유하는 제약조성물.
  8. 제1 내지 3항 및 6항의 어느 항에 따르는 화합물을 심장 및 순환기 질환의 치료를 위한 사용.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019890002324A 1988-02-27 1989-02-27 삼치환된 아민 이들의 제법 및 이들을 함유하는 제약조성물 KR890012990A (ko)

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US4921713A (en) * 1987-06-05 1990-05-01 Fowler Daniel L Versatile controlled flavor straw assembly
DE3928247A1 (de) * 1989-08-26 1991-02-28 Boehringer Mannheim Gmbh Neue optisch aktive basische ether, verfahren zu ihrer herstellung sowie arzneimittel, die diese verbindungen enthalten
JPH03133946A (ja) * 1989-10-10 1991-06-07 Glaxo Group Ltd フェンエタノールアミン化合物
US5610183A (en) * 1991-07-10 1997-03-11 Merck, Sharp & Dohme Ltd. Phenylglycine derivatives pharmaceutical compositions containing them and their use in therapy
GB9211193D0 (en) * 1992-05-27 1992-07-08 Merck Sharp & Dohme Therapeutic agents
WO1994003429A1 (en) * 1992-07-31 1994-02-17 Merck Sharp & Dohme Limited Substituted amines as tachykinin receptor antagonists
US5747523A (en) * 1996-01-24 1998-05-05 Guilford Pharmaceuticals Inc. Substituted ethyl α,α-diarylmethyl ether derivatives

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US2774767A (en) * 1954-05-03 1956-12-18 Hoechst Ag Process of preparing 2-phenyl-2-pyridyl-(4')-4-diloweralkyl amino butyric lower alkyl esters
NL92722C (ko) * 1956-02-09
GB1050177A (ko) * 1963-07-18
GB1237352A (en) * 1969-01-03 1971-06-30 Ct Europ De Rech S Mauvernay Substituted propylamines
FR2223006A1 (en) * 1973-03-28 1974-10-25 Ugine Kuhlmann Substd. iso-propyl nicotinates - antiarrhythmic and hypolipemic agents prepd. from nicotinoyl chloride and a substd iso-propanol
FR2273532A1 (fr) * 1974-06-06 1976-01-02 Synthelabo Nouveaux derives du thienyl-2 acetonitrile, leurs sels, leur preparation et les medicaments qui en contiennent
DE3726633A1 (de) * 1987-08-11 1989-02-23 Boehringer Mannheim Gmbh Neue 1,2-diamino-verbindungen, verfahren zu ihrer herstellung sowie arzneimittel, die diese verbindungen enthalten

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CS108389A2 (en) 1990-08-14
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IL89395A0 (en) 1989-09-10
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NZ228046A (en) 1991-04-26
DE3806321A1 (de) 1989-09-07
JPH023633A (ja) 1990-01-09
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US4999361A (en) 1991-03-12
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DK90189D0 (da) 1989-02-24
NO890803L (no) 1989-08-28
CN1035506A (zh) 1989-09-13
CS274445B2 (en) 1991-04-11
HUT50800A (en) 1990-03-28
ZA891435B (en) 1989-11-29

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