KR890008101A - β-아드레날린성 애고니스트 - Google Patents

β-아드레날린성 애고니스트 Download PDF

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KR890008101A
KR890008101A KR1019880015592A KR880015592A KR890008101A KR 890008101 A KR890008101 A KR 890008101A KR 1019880015592 A KR1019880015592 A KR 1019880015592A KR 880015592 A KR880015592 A KR 880015592A KR 890008101 A KR890008101 A KR 890008101A
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amino
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lower alkyl
methyl
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에이취.피셔 마이클
제이.와이브랜트 2세 매뉴
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제임스 에프.노오톤
머크 앤드 캄파니 인코포레이티드
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Abstract

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Description

β-아드레날린성 애고니스트
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (22)

  1. 하기 일반식(I)의 화합물 및 이의 약제학적으로 허용되는 산부가염
    상기식에서, R₁,R₂ 및 R₃는 수소이거나, 또는 하이드록시 또는 저급 알콕시에 의해 임의로 치환될 수 있는 저급 알킬, 저급 알케닐 및 저급 알키닐중에서 독립적으로 선택되거나, 또는 R₁ 및 R₂는 결합되어 저급 알킬에 의해 추가로 치환될 수 있는 3 내지 6원의 사이클릭환을 형성할 수 있고 : Het는 하기 일반식(a) 내지(f)의 그룹중에서 선택된다
    [여기서, R₄ 및 R5는 독립적으로 수소, 저급 알킬, 페닐, 치환된 페닐, 페닐저급알킬 또는 치환된 페닐저급알킬(여기에서, 치환체는 저급알킬, 저급알콕시 또는 할로이다)이다]
  2. 제 2 항에 있어서, R₁,R₂ 및 R₃가 수소, 저급 알킬, 저급 알케닐 및 저급 알키닐중에서 독립적으로 선택되거나, 또는 R₁ 및 R₂는 결합되어 3내지 6원의 사이클릭 환을 형성할 수 있고 : Het가 일반식(a),(b),(c),(d) 및 (e)의 그룹중에서 선택되며 : R÷가 수소 또는 저급 알킬이고 : R5가 탄소수 1내지 3의 저급 알킬인 화합물
  3. 제 2 항에 있어서, R₁,R₂ 및 R₃가 저급 알킬중에서 독립적으로 선택되거나, R₃가 수소 또는 저급 알킬이며 R₁ 및 R₂는 결합되어 3내지 4원의 사이클릭 환을 형성할 수 있고 : Het가 일반식(a),(b) 및 (c),(d) 및 (e)의 그룹중에서 선택되고 : R÷가 수소 또는 탄소수 1내지 3의 저급 알킬인 화합물
  4. 제 3 항에 있어서, R₁,R₂ 및 R₃가 탄소수 1내지 3의 저급 알킬중에서 독립적으로 선택되며 : Het가 3위치에서 에틴올아민 부위에 결합된 일반식(a)의 그룹이고 : R₄가 수소인 화합물
  5. 제 1 항에 있어서, 이의 염산 또는 말레인산 염인 화합물
  6. 제 1 항에 있어서, (R)-6-아미노-a-[[(1,1-디메틸에틸)아미노]메틸]-3-피리딘메탄올인 화합물
  7. 제 1 항에 있어서, (R)-6-아미노-a-[[(1-메틸에틸)아미노]메틸]-3-피리딘메탄올인 화합물
  8. 제 1 항에 있어서, (R)-6-아미노-a-[[(1,1-디메틸프로필)아미노]메틸]-3-피리딘메탄올인 화합물
  9. 제 1 항에 있어서, (R)-6-아미노-a-[[(사이클로부틸)아미노]메틸]-3-피리딘메탄올인 화합물
  10. 제 1 항에 있어서, (R)-6-아미노-a-[[(1,1-메틸에틸)아미노]메틸]-3-피리딘메탄올인 화합물
  11. 제 1 항에 있어서, (R)-6-아미노-a-[[(1,1-사이클로부틸)아미노]메틸]-3-피리딘메탄올인 화합물
  12. 제 1 항에 있어서, (R)-6-아미노-a-[[(1,1-메틸사이클로부틸)아미노]메틸]-3-피리딘메탄올인 화합물
  13. 제 1 항에 있어서, (R)-6-아미노-a-[[(1,1-디메틸에틸)아미노]메틸]-3-피리딘메탄올인 화합물
  14. 제 1 항에 있어서, (R)-6-아미노-a-[[(1,1-디메틸에틸)아미노]메틸]-5-피리딘메탄올인 화합물
  15. 하기 일반식(4)의 화합물을 염화주석(II)과 방응시킨을 특징으로하여, 제 1 항에서 정의한 하기 일반식(6)의 화합물을 제조하는 방법
    상기식에서 R₁, R₂ 및 R₃는 제 1 항에서 정의한 바와 같다
  16. 적절하게 보호된 하기 일반식(6)의 화합물을 온화한 산화제로 처리함을 특징으로하여, 제 1 항에서 정의한 하기 일반식(7)의 화합물을 제조하는 방법
    상기식에서, R₁, R₂ 및 R₃는 제 1 항에서 정의한 바와 같다
  17. 하기 일반식(3)의 화합물을 과량의 아민 H₂NCR₁R₂R₃으로 처리한후, 중간체인 아민화된 케톤을 환원기키거나, 또는 하기 일반식(5)의 에폭사이드 화합물을 과량의 아민 H₂NCR₁R₂R₃으로 처리함을 특징으로 하여, 제 1 항에서 정의한 하기 일반식(4)의 화합물을 제조하는 방법
    상기식에서, R₁, R₂ 및 R₃는 제 1 항에서 정의한 바와 같다
  18. 제17항에 있어서, 에폭사이드 화합물이 R-이성체인 방법
  19. 하기 일반식(14)의 화합물을 과량의 아민H₂NCR₁R₂R₃으로 처리한후, 중간체인 아민화된 케톤을 환원시키거나, 또는 하기 일반식(13)의 화합물을 과량의 아민 H₂NCR₁R₂R₃으로 처리함을 특징으로 하여, 제 1 항에서 정의한 하기 일반식(4)의 화합물을 제조하는 방법
    상기식에서, R₁, R₂ R₃R₄ 및 R5는 제 1 항에서 정의한 바와 같고, A는 탄소 또는 질소 환원자이다
  20. 하기 일반식(15)의 화합물을 산 또는 염기 촉매하에서 가수분해시킴을 특징로하여, 제 1 항에서 정의한 하기 일반식(16)의 화합물을 제조하는 방법
    상기식에서, R₁, R₂ R₃R5및 R5는 제 1 항에서 정의한 바와 같고, A는 탄소 또는 질소 원자이다
  21. 동물에 유효량의 제 1 항에 화합물을 투여함을 특징으로하여 동물의성장을 촉진시키며 사료 효율을 증가시키는 방법
  22. 불활성 담체 및 제 1 항의 화합물을 함유함을 특징으로하는, 동물의 성장 촉진과 사료 효율을 증가 시키는데 유용한 조성물
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019880015592A 1987-11-27 1988-11-26 β-아드레날린성 애고니스트 KR890008101A (ko)

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GB201714745D0 (en) * 2017-09-13 2017-10-25 Atrogi Ab New compounds and uses
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JP2022538907A (ja) * 2019-07-01 2022-09-06 キュラセン セラピューティクス インコーポレイテッド βアドレナリンアゴニストおよびその使用方法

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EP0105053B1 (en) * 1982-10-01 1988-01-20 Merck & Co. Inc. Aralkylaminoethanol heterocyclic compounds
NZ212204A (en) * 1984-06-04 1988-07-28 Merck & Co Inc Growth-promoting compositions containing hydroxylic compounds
DE3615293A1 (de) * 1986-05-06 1987-11-12 Bayer Ag Verwendung von heteroarylethylaminen zur leistungsfoerderung bei tieren, heteroarylethylamine und verfahren zu ihrer herstellung
DE3813839A1 (de) * 1988-04-23 1989-11-02 Bayer Ag 4-brom-6-chlor-5-amino-2-pyridil-ethanolamine verfahren zu ihrer herstellung u. ihre verwendung als leistungsfoerderer

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DK659688A (da) 1989-07-31
NZ226991A (en) 1992-03-26
EP0318092A3 (en) 1989-11-23
EP0318092A2 (en) 1989-05-31
PT89085A (pt) 1988-12-01
AU2592988A (en) 1989-06-01
PT89085B (pt) 1993-03-31
DK659688D0 (da) 1988-11-25
AU613681B2 (en) 1991-08-08
JPH01186867A (ja) 1989-07-26

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