KR930004262A - 메타노안트라센 화합물 - Google Patents

메타노안트라센 화합물 Download PDF

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KR930004262A
KR930004262A KR1019920014726A KR920014726A KR930004262A KR 930004262 A KR930004262 A KR 930004262A KR 1019920014726 A KR1019920014726 A KR 1019920014726A KR 920014726 A KR920014726 A KR 920014726A KR 930004262 A KR930004262 A KR 930004262A
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톰즈 제이컵스 로버트
테디어스 클리마스 마이클
존 오마크트 사이러스
오널 터프코 마크
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수잔 제인 젠틀
임페리얼 케미칼 인더스트리스 피엘씨
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    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
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    • 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
    • C07D211/40—Oxygen atoms
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    • 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
    • C07D211/40—Oxygen atoms
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    • C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond

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Abstract

내용 없음.

Description

메타노안트라센 화합물
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (9)

  1. 하기 일반식(Ⅰ)의 화합물 또는 그것의 약학적으로 허용가능한 염.
    상기 식에서 X와 Y는 각각 수소, 할로, 및 (1-6C)알콕시중에서 선택되고, R1은 (A) (1-6C)알킬, (B) 각각 (1-6C)알킬, (1-6C)알콕시, 히드록시, 할로, 시아노, 니트로, 페닐, 벤질옥시, 벤조일, 트리플루오로메틸, 일반식 SO2NRaRb로 표시되는 아미노설포닐, 및 일반식 CONRcRd로 표시되는 아미노카르보닐(이때 Ra, Rb, Rc및 Rd는 각각 수소, 2-피롤리디닐, 및 (1-6C)알킬중에서 선택되거나, 또는 Ra와 Rb, 및 Rc와 Rd는 이들이 각각 결합하고 있는 질소 원자와 함께 5-원소 또는 6-원소로 구성된 헤테로사이클계 링을 형성하며, 상기 질소 원자는 유일한 이종 원자이다), 및 RhRiN(1-3C)알킬(이때 Rh와 Ri는 각각 수소 및 (1-3C)알킬중에서 선택된다)로 이루어진 군중에서 선택된 0-3개의 치환기를 가질 수 있는 페닐 및 나트틸, (C) 페닐(1-3C)알킬 및 나프틸(1-3C)알킬(이때 페닐 및 나프틸기는 상기 (B)에 주어진 페닐 및 나프틸 치환기 중에서 선택된 0-3개의 치환기를 가질 수 있다), (D) 질소, 산소, 및 황중에서 선택된 1-3개의 이종 원자를 함유하고, (1-6C)알킬, 히드록시, 트리플루오로메틸기를 가질 수 있는 (1-6C)알콕시, (1-6C)알콕시카르보닐, (1-6C)히드록시알킬, 벤질옥시, 할로, (1-3C) 알킬아미노카르보닐(1-3C)알킬, 상기 (B)에서 정의한 바와 같은 아미노카르보닐, ReS(O)n, RfNH 및 RgS중에서 선택된 0-2개의 치환기를 가질 수 있는, 5-원소 및 6-원소로 구성된 헤테로아릴링, 또는 이것의 벤즈유도체(이때 Re와 Rf는 각각 수소 및 (1-6C)알킬중에서 선택되고 n은 0, 1 또는 2이며, Rg는 (1-3C)알킬카르보닐아미노페닐 및 디(1-3C)알킬아미노 (1-6C)알킬중에서 선택된다), (E) 헤테로아릴기가 상기 (D)에서 정의한 바와 같은 5-원소 또는 6-원소로 구성된 링이고, 상기 (D)에 주어진 헤테로아릴 치환기의 의미중에서 선택된 0-2개의 치환기를 가질 수 있는 헤테로아릴(1-3C)알킬중에서 선택된다.
  2. 제1항에 있어서, X 및 Y가 각각 수소 및 할로중에서 선택되는 화합물.
  3. 제2항에 있어서, X와 Y는 각각 수소 및 클로로중에서 선택되고, R1이 (i) t-부틸, (ii) 2-메톡시페닐, 3-메톡시페닐, 및 일반식 RaRbNSO2(이때 Ra와 Rb는 각각 수소, 메틸 및 에틸중에서 선택된다)로 표시되는 아미노설포닐에 의해 2- 또는 3- 위치가 치환된 페닐, (iii) 티에닐, 푸릴, 및 2-위치가 (1-6C)알콕시, (1-6C)알킬티오, 또는 (1-6C)알킬설피닐에 의해 임의로 치환된 37피리딜로 이루어진 군중에서 선택되는 화합물.
  4. 제3항에 있어서, 1-((9S,10S)-2-클로로-9,10-디하이드로-9,10-메타노안트라센-9-일-메틸)-4-(1,1-대메틸에틸)피페리딘-4-올, 1-(9,10-디하이드로-9,10-메타노안트라센-9-일메틸)-4-(2-에틸설피닐-3-피리딜)피페리딘-4-올, 1-(9,10-디하이드로-9,10-메타노안트라센-9-일메틸)-4-(2-에틸티오-3-피리딜)피페리딘-4-올, 및 1-(2-클로로-9,10-디하이드로-9,10-메타노안트라센-9-일-메틸)-4-(2-메톡시-3-피리딜)피페리딘-4-올 중에서 선택되는 화합물.
  5. 제1항 내지 제4항중 어느 한 항에 있어서 정의한 일반식(Ⅰ)의 화합물과 약학적으로 허용가능한 부형제 또는 담체를 포함하는 약학 조성물.
  6. 하기 일반식(II)의 화합물.
    상기 식에서 X와 Y는 각각 수소, 할로, 및 (1-6C)알콕시중에서 선택된다.
  7. 하기 일반식(IIa)의 화합물.
    상기 식에서 X, Y 및 R1은 제1항에서 정의한 바와 같다.
  8. 하기 일반식(III)의 화합물.
    상기 식에서 X와 Y는 각각 수소, 할로, 및 (1-6C)알콕시중에서 선택되고, G는 G가 H 또는 OH일때 X와 Y는 둘다 H가 아니라는 조건하에, 클로로, OH 및 H중에서 선택된다.
  9. a) 하기 일반식(Ⅱ)로 표시되는 화합물을 비양성자성 용매중에서 일반식1Li로 표시되는 상응하는 화합물로 처리하거나, (b) 하기 일반식(IIa)의 상응하는 아미드를 적합한 환원제로 처리하거나, (c) G가 수소 원자인 하기 일반식(III)의 알데히드를 환원제의 존재하에 하기 일반식(IV)의 상응하는 피페리딘으로 처리하거나, (d) X와 Y중 어느 하나가 (1-6C)알콕시인 일반식(Ⅰ)의 화합물을 제조하고자 하는 경우에는, X 또는 Y가 히드록시인 상응하는 일반식(Ⅰ)의 화합물을 염기의 존재하에, 상응하는 (1-6C)알킬 할라이드로 처리하고, 그 후에 약학적으로 허용가능한 염을 제조하고자 하는 경우에는, 상기 화합물을 적합한 산과 함께 통상적인 방법으로 반응시키는 것을 특징으로 하는, 일반식(Ⅰ)의 화합물, 또는 그것의 약학적으로 허용가능한 염을 제조하는 방법.
    상기 식에서, X, Y 및 R1은 제1항에서 정의한 바와 같다.
    ※참고사항:최초출원 내용에 의하여 공개하는 것임.
KR1019920014726A 1991-08-15 1992-08-14 메타노안트라센화합물 KR100245955B1 (ko)

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FI102964B (fi) 1999-03-31
JP2889056B2 (ja) 1999-05-10
CA2076191A1 (en) 1993-02-16
ATE144253T1 (de) 1996-11-15
CZ283848B6 (cs) 1998-06-17
HUT66625A (en) 1994-12-28
HU9202643D0 (en) 1992-10-28
DE69214588T2 (de) 1997-05-28
IL102807A0 (en) 1993-01-31
IL102807A (en) 1998-08-16
SK280356B6 (sk) 1999-12-10
GB9216296D0 (en) 1992-09-16
CZ251992A3 (en) 1993-02-17
AU658905B2 (en) 1995-05-04
FI102964B1 (fi) 1999-03-31
GB9117639D0 (en) 1991-10-02
NZ243955A (en) 1995-10-26
TW221808B (ko) 1994-03-21
DK0533344T3 (ko) 1997-03-03
IE922588A1 (en) 1993-02-24
KR100245955B1 (ko) 2000-04-01
FI923663A0 (fi) 1992-08-14
NO923199D0 (no) 1992-08-14
ZA926148B (en) 1993-04-28
HK83697A (en) 1997-06-27
JPH05213872A (ja) 1993-08-24
FI923663A (fi) 1993-02-16
ES2092646T3 (es) 1996-12-01
SG48140A1 (en) 1998-04-17
EP0533344A1 (en) 1993-03-24
BG61893B2 (bg) 1998-08-31
NO301008B1 (no) 1997-09-01
AU2101492A (en) 1993-02-18
GR3021398T3 (en) 1997-01-31
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SK251992A3 (en) 1999-12-10
NO923199L (no) 1993-02-16
HU211661A9 (en) 1995-12-28
RU2099328C1 (ru) 1997-12-20

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