KR970021076A - 약제학적 활성 성분으로서 치환된 2,4-이미다졸리딘디온 화합물 - Google Patents

약제학적 활성 성분으로서 치환된 2,4-이미다졸리딘디온 화합물 Download PDF

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KR970021076A
KR970021076A KR1019960048441A KR19960048441A KR970021076A KR 970021076 A KR970021076 A KR 970021076A KR 1019960048441 A KR1019960048441 A KR 1019960048441A KR 19960048441 A KR19960048441 A KR 19960048441A KR 970021076 A KR970021076 A KR 970021076A
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alkyl
formula
compound
substituted
phenyl
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KR1019960048441A
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KR100445539B1 (ko
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마사토시 시모무라
미아키 아사카와
유이치 기타
오스발트 침머
호르스트 뵐케
슈테판 브넨트
코르넬리아 가이스트
카이 츠빈겐베르거
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아이다 겐지
가부시키가이샤 니혼쇼쿠바이
비르츠 프란츠, 파우쓰-베르구스
그뤼넨탈 게엠베하
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/08Antiepileptics; Anticonvulsants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/04Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic 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
    • C07D417/02Heterocyclic 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
    • C07D417/04Heterocyclic 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

Abstract

본 발명은 2,4-이미다졸리딘디온 화합물, 이의 제조방법 및 약제학적 제제에서의 이들 화합물의 용도에 관한 것이다.

Description

약제학적 활성 성분으로서 치환된 2,4-이미다졸리딘디온 화합물
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (12)

  1. 화학식 (1)의 치환된 2,4-이미다졸리딘디온 화합물.
    상기 화학식에서, R1은 C1-6알킬 또는 C3-6사이클로알킬이고, R2는 C1-6알킬, 페닐, -(CH2)1-3-페닐 또는 -(CH2)1-4-COOR5이거나 R1및 R2가 함께는 -(CH2)4-6-, -(CH2)2-0-(CH2)2- 또는 화학식
    이거나, R3이 H, C1-5알킬 또는 -(CH2)1-4-COOR5이며, R4가 화학식
    의 그룹으로부터 선택된 헤테로방향족 그룹이며, R5는 C1-3알킬이고, R6는 H, C1-4알킬, 페닐 또는 벤질이며, R7은 H, C1-4알킬 또는 트리플루오로메틸이다.
  2. 제1항에 있어서, R1이 C1-4알킬 또는 C3-4사이클로알킬이고, R2가 C3-6알킬, 페닐, -(CH2)1-2-페닐 또는 -(CH2)1-2-COOR5이거나, R1및 R2가 함께는 -(CH2)5- 또는 화학식
    이고, R3이 H, C1-4알킬 또는 -(CH2)1-2-COOR5이며, R4가 화학식
    의 그룹으로부터 선택된 헤테로방향족 그룹이며, R5가 C1-3알킬이고, R6이 H 또는 페닐이며, R7이 H, 메틸, 3급 부틸 또는 트리플루오로메틸임을 특징으로 하는, 화학식 (1)의 치환된 2,4-이미다졸리딘디온 화합물.
  3. 제1항 또는 제2항에 있어서, R1이 에틸 또는 사이클로부틸이고, R2가 페닐이거나, R1및 R2가 함께는 -(CH2)5-임을 특징으로 하는, 화학식 (1)의 치환된 2,4-이미다졸리딘디온 화합물.
  4. 제1항 내지 제3항중 어느 한 항에 있어서, R1및 R2가 함께 -(CH2)5-임을 특징으로 하는, 화학식 (1)의 치환된 2,4-이미다졸리딘디온 화합물.
  5. 제1항 내지 제4항중 어느 한 항에 있어서, R3이 H, C1-3알킬 또는 -CH2-COOR5이고, R5가 에틸임을 특징으로 하는, 화학식 (1)의 치환된 2,4-이미다졸리딘디온 화합물.
  6. 제5항에 있어서, R3이 H임을 특징으로 하는, 화학식 (1)의 치환된 2,4-이미다졸리딘디온 화합물.
  7. 제1항 내지 제6항중 어느 한 항에 있어서, R4가 피리딘-4-일, 피리딘-3일, 티아졸-2-일, 3-메틸이속사졸-5-일 또는 5-메틸이속사졸-3-일임을 특징으로 하는, 화학식 (1)의 치환된 2,4-이미다졸리딘디온 화합물.
  8. 제7항에 있어서, R4가 티아졸-2-일임을 특징으로 하는, 화학식 (1)의 치환된 2,4-이미다졸리딘디온 화합물.
  9. 화학식 (2)의 아민이 1,1′-카보닐디이미다졸 또는 디페닐 카보네이트를 가한 후 화학식 (3)의 화합물과 반응시켜 R3이 H인 화학식 (1)의 화합물을 수득하고, 경우에 따라, 이 화합물을 탈양자화한 후 화학식 (4)의 화합물 또는 화학식 (5)의 화합물과 반응시켜 R3이 C1-5알킬 또는 -(CH2)1-4-COOR5인 화학식 (1)의 화합물을 수득함을 특징으로 하는, 화학식 (1)의 치환된 2,4-이미다졸리딘디온 화합물의 제조 방법.
    상기 화학식에서, R1은 C1-6알킬 또는 C3-6사이클로알킬이고, R2는 C1-6알킬, 페닐, -(CH2)1-3-페닐 또는 -(CH2)1-4-COOR5이거나 R1및 R2가 함께는 -(CH2)4-6-, -(CH2)2-0-(CH2)2- 또는 화학식
    이거나, R3은 H, C1-5알킬 또는 -(CH2)1-4-COOR5이고, R4는 화학식
    의 그룹으로부터 선택된 헤테로방향족 그룹이며, R5는 C1-3알킬이고, R6는 H, C1-4알킬, 페닐 또는 벤질이며, R7은 H, C1-4알킬 또는 트리플루오로메틸이고, R8은 H 또는 C1-3알킬이며, X는 Cl, Br 또는 I이다.
  10. 약제학적 제제중 활성 성분으로서의, 제1항에 다른 화학식 (1)의 치환된 2,4-이미다졸리딘디온 화합물의 용도.
  11. 제10항에 있어서, 약제학적 제제가 면역조절제임을 특징으로 하는 용도.
  12. 제10항에 있어서, 약제학적 제제가 항맥관염 작용을 갖는 것을 특징으로 하는 용도.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019960048441A 1995-10-27 1996-10-25 치환된2,4-이미다졸리딘디온화합물및이를함유하는약제학적조성물 KR100445539B1 (ko)

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DE19540027.5 1995-10-27
DE19540027A DE19540027A1 (de) 1995-10-27 1995-10-27 Substituierte Imidazolidin-2,4-dion-Verbindungen als pharmazeutische Wirkstoffe
JP7-283270 1995-10-31

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Families Citing this family (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19732928C2 (de) * 1997-07-31 2000-05-18 Gruenenthal Gmbh Verwendung substituierter Imidazolidin-2,4-dion-Verbindungen als Schmerzmittel
DE19917961A1 (de) 1999-04-21 2000-10-26 Degussa Verfahren zur Herstellung von Aminosäurederivaten
WO2001007048A1 (en) * 1999-07-21 2001-02-01 Boehringer Ingelheim Pharmaceuticals, Inc. Small molecules useful in the treatment of inflammatory disease
ES2284641T3 (es) 2000-05-31 2007-11-16 Tanabe Seiyaku Co., Ltd. Inhibidores de la adhesion celular mediada por alfa-l-beta-2.
US7354933B2 (en) 2003-01-31 2008-04-08 Aventis Pharma Sa Cyclic urea derivatives, preparation thereof and pharmaceutical use thereof as kinase inhibitors
FR2850652B1 (fr) * 2003-01-31 2008-05-30 Aventis Pharma Sa Nouveaux derives d'uree cyclique, leur preparation et leur utilisation pharmaceutique comme inhibiteurs de kinases
WO2005090316A1 (en) * 2004-03-12 2005-09-29 Wyeth HYDANTOINS HAVING RNase MODULATORY ACTIVITY
EP1621536A1 (en) * 2004-07-27 2006-02-01 Aventis Pharma S.A. Amino cyclic urea derivatives, preparation thereof and pharmaceutical use thereof as kinase inhibitors
EP1621539A1 (en) * 2004-07-27 2006-02-01 Aventis Pharma S.A. Heterocycle -substituted cyclic urea derivatives, preparation thereof and pharmaceutical use thereof as kinase inhibitors
EP1621535A1 (en) * 2004-07-27 2006-02-01 Aventis Pharma S.A. Substituted cyclic urea derivatives, preparation thereof and pharmaceutical use thereof as kinase inhibitors
US7709517B2 (en) 2005-05-13 2010-05-04 The Regents Of The University Of California Diarylhydantoin compounds
FR2896504B1 (fr) * 2006-01-23 2012-07-13 Aventis Pharma Sa Nouveaux derives d'uree cyclique, leur preparation et leur utilisation pharmaceutique comme inhibiteurs de kinases
FR2896503B1 (fr) * 2006-01-23 2012-07-13 Aventis Pharma Sa Nouveaux derives soufres d'uree cyclique, leur preparation et leur utilisation pharmaceutique comme inhibiteurs de kinases
AU2012241184B2 (en) * 2006-03-27 2016-01-07 The Regents Of The University Of California Androgen receptor modulator for the treatment of prostate cancer and androgen receptor-associated diseases
AU2016201061B2 (en) * 2006-03-27 2017-03-02 The Regents Of The University Of California Androgen receptor modulator for the treatment of prostate cancer and androgen receptor-associated diseases
AU2013205325B2 (en) * 2006-03-27 2016-03-24 The Regents Of The University Of California Androgen receptor modulator for the treatment of prostate cancer and androgen receptor-associated diseases
EP3412290B1 (en) * 2006-03-27 2021-03-03 The Regents of The University of California Androgen receptor modulator for the treatment of prostate cancer and androgen receptor-associated diseases
CN101460467B (zh) * 2006-03-29 2012-09-19 加利福尼亚大学董事会 二芳基硫代乙内酰脲化合物
WO2008021309A1 (en) * 2006-08-15 2008-02-21 Wyeth Imidazolidin-2-one derivatives useful as pr modulators
US7649007B2 (en) * 2006-08-15 2010-01-19 Wyeth Llc Oxazolidine derivatives as PR modulators
WO2008021337A1 (en) 2006-08-15 2008-02-21 Wyeth Oxazinan-2-one derivatives useful as pr modulators
TW200815428A (en) 2006-08-15 2008-04-01 Wyeth Corp Oxazolidone derivatives as PR modulators
CA2661315C (en) * 2006-09-08 2015-11-24 Actelion Pharmaceuticals Ltd Pyridin-3-yl derivatives as immunomodulating agents
JP5535925B2 (ja) 2007-10-26 2014-07-02 ザ リージェンツ オブ ザ ユニバーシティ オブ カリフォルニア アンドロゲン受容体調節物質としてのジアリールヒダントイン化合物
SG192439A1 (en) * 2008-06-27 2013-08-30 Novartis Ag Organic compounds
RS53075B (en) 2009-05-12 2014-04-30 Janssen Pharmaceuticals Inc. 1,2,4-TRIAZOLO [4,3-A] PYRIDINE DERIVATIVES AND THEIR USE IN THE TREATMENT OR PREVENTION OF NEUROLOGICAL AND PSYCHIATRIC DISORDERS
SI3124481T1 (en) 2010-02-16 2018-06-29 Aragon Pharmaceuticals, Inc. Androgen receptor modulators and their use
MY180834A (en) 2012-09-26 2020-12-10 Aragon Pharmaceuticals Inc Anti-androgens for the treatment of non-metastatic castrate-resistant prostate cancer
JOP20200097A1 (ar) 2013-01-15 2017-06-16 Aragon Pharmaceuticals Inc معدل مستقبل أندروجين واستخداماته
TWI726969B (zh) 2016-01-11 2021-05-11 比利時商健生藥品公司 用作雄性激素受體拮抗劑之經取代之硫尿囊素衍生物
AU2018351714A1 (en) 2017-10-16 2020-04-30 Aragon Pharmaceuticals, Inc. Anti-androgens for the treatment of non-metastatic castration-resistant prostate cancer

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0091596B1 (de) * 1982-04-08 1991-09-11 Shell Internationale Researchmaatschappij B.V. Neue Hydantoine, ihre Herstellung und Verwendung
US4746669A (en) * 1985-12-23 1988-05-24 Merck & Co., Inc. Substituted thiazoles as immunoregulants
JPH02101065A (ja) * 1988-10-06 1990-04-12 Tanabe Seiyaku Co Ltd イミダゾリン誘導体及びその製法
EP0557408A4 (en) * 1990-11-06 1993-10-27 Smith-Kline Beecham Corporation Imidazolidinone compounds
IL110296A (en) * 1993-07-16 1999-12-31 Smithkline Beecham Corp Imidazole compounds process for their preparation and pharmaceutical compositions containing them
US7466669B2 (en) * 2003-11-14 2008-12-16 Telefonaktiebolaget Lm Ericsson (Publ) Reverse link scheduler for CDMA networks

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CO4750655A1 (es) 1999-03-31
HU222120B1 (hu) 2003-04-28
KR100445539B1 (ko) 2004-12-30
EP0770613A1 (de) 1997-05-02
ZA968956B (en) 1997-05-29
IL119488A0 (en) 1997-01-10
IL119488A (en) 2001-01-11
HK1010367A1 (en) 1999-06-17
DE19540027A1 (de) 1997-04-30
SI0770613T1 (en) 1999-10-31
MX9605023A (es) 1997-06-28
HUP9602932A3 (en) 1998-08-28
CN1152573A (zh) 1997-06-25
ATE181072T1 (de) 1999-06-15
AR004517A1 (es) 1998-12-16
AU707751B2 (en) 1999-07-22
EP0770613B1 (de) 1999-06-09
RU2163603C2 (ru) 2001-02-27
CN1097050C (zh) 2002-12-25
AU6818196A (en) 1997-05-01
GR3030558T3 (en) 1999-10-29
DE59602155D1 (de) 1999-07-15
PL316706A1 (en) 1997-04-28
ES2135148T3 (es) 1999-10-16
PL184446B1 (pl) 2002-10-31
HU9602932D0 (en) 1996-12-30
DK0770613T3 (da) 1999-12-13
CA2188908A1 (en) 1997-04-28
HUP9602932A2 (hu) 1998-07-28
PE20011055A1 (es) 2001-12-29
JPH09188677A (ja) 1997-07-22
US6004963A (en) 1999-12-21

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