KR920016443A - 2,4-및 2,5-비스테트라졸릴피리딘, 이의 제조방법 및 약제로서의 이의 용도 - Google Patents

2,4-및 2,5-비스테트라졸릴피리딘, 이의 제조방법 및 약제로서의 이의 용도 Download PDF

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KR920016443A
KR920016443A KR1019920001589A KR920001589A KR920016443A KR 920016443 A KR920016443 A KR 920016443A KR 1019920001589 A KR1019920001589 A KR 1019920001589A KR 920001589 A KR920001589 A KR 920001589A KR 920016443 A KR920016443 A KR 920016443A
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alkyl
compound
collagen
cycloalkyl
alkenyl
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KR1019920001589A
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KR100214797B1 (ko
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슈베르트 게리트
바더 엑케하르트
빅켈 마르틴
귄즐러-푸칼 볼크마르
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엥겔하르트, 라피세
훽스트 아크티엔게젤샤프트
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/02—Heterocyclic 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
    • C07D401/04—Heterocyclic 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/14—Heterocyclic 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 three or more hetero rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
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  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
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  • Diabetes (AREA)
  • Hematology (AREA)
  • Transplantation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pyridine Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Abstract

내용 없음

Description

2,4- 및 2,5-비스테트라졸릴피리딘, 이의 제조방법 및 약제로서의 이의 용도
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (14)

  1. 일반식(Ⅰ)의화합물 및 생리학적으로 허용되는 이의 염.
    (Ⅰ)
    상기식에서,
    A는또는이고,
    B는 H;(C1-C6)알킬, (C2-C6)알케닐, (C2-C6)알키닐, (C2-C6)아릴, Ar(C6-C10)알킬(하나 이상의 CH2그룹은N ,O 또는S와같은 헤테로 원자에 의해 임의로 대체된다), 사이클로알킬-또는 사이클로알케닐(C0-C6)알킬(사이클 내의 1내지 3개의 CH2그룹은 O , S또는N과 같은 헤테로원자 또는 C = O 와 같은 그룹에 의해 대체된다)이다.
  2. 제1항에 있어서, R이 H;(C1-C6)알킬, (C2-C6)알케닐, (C2-C6)알키닐(이들은 각각 카복실 또는 카복시(C1-C4)알킬에스테르, 아릴카보닐, (C1-C4)알킬아미노카보닐, 카보닐, 특히 아미노카보닐에 의해 치환된다)인 화합물.
  3. 제1항 또는 2항에 있어서, R이 (C2-C6)알킬, (C2-C6)알케닐, (C2-C6)알키닐[이들은 페닐카복실, (C1-C4)알킬아미노카보닐, 알킬에 대해 (C1-C6)알콕시에 의한 치환이 가능한 경우 아미노카보닐(이때 질소는 1개, 바람직하게는 2개의 알킬, 특히(C1-C3)알킬에 의해 치환된다)에 의해 치환된다]인 화합물.
  4. 제1항에 있어서, R이 (C6-C10)아릴, 특히 페닐 또는 나프틸 [이는 할로겐(염소 또는 브롬)에 의해 임의로 치환된다]인 화합물.
  5. 제1항에 있어서, R이 Ar(C2-C6)알킬(여기에서 알킬 라디칼 내의 1개 또는 2개의 CH2그룹은 N,O또는 S중에서 선택된 헤테로원자에 의해 대체되고, Ar은 페닐이다)인 화합물.
  6. 제1항에 있어서, R이 사이클로알킬-또는 사이클로알케닐 (C0-C6)알킬, 특히 (C5-C6)사이클로알킬-또는 -알케닐(C0-C3)-알킬(여기에서 사이클은 알킬, 특히(C1-C4)알킬에 의해 치환된다)인 화합물.
  7. 제1항 또는 6항에 있어서, R이 사이클로알킬-또는 사이클로알케닐 (C0-C6)알킬인 경우 축방향으로 대칭적인 화합물
  8. 제1항 내지 7항에 있어서, 라디칼 R이 두 치환체 모두에 대해 동일한 화합물.
  9. 제8항에 있어서, A에 대한 치환 양상(2,4 또는 2,5)이 동일한 화합물.
  10. 일반식(Ⅱ)의 화합물을 적합한 유기 용매중에서 NaN3및 NH4Cl과 반응시킨 후 경우에 따라 치환 반응으로 목적하는 치환제를 도입시킴을 특징으로 하여, 제1항내지 9항에 따른 화합물을 제조하는 방법.
    (Ⅱ)
  11. 프롤린 하이드록실라제 및 리신 하이드록실라제를 억제하기 위한 제1항 내지 10항에 따른 화합물.
  12. 섬유억제제(fibrosuppressant)및 면역억제제로서 사용하기 위한 제1항 내지 10항에 따른 화합물.
  13. 제1항에 따른 화합물 및/또는 생리학적으로 허용되는 이의 염을 함유하는 콜라겐 및 콜라겐-유사물질의 생합성 및 Clq의 생합성의 장애를 치료하기 위한 약제.
  14. 제1항에 따른 일반식(Ⅰ)의 화합물 및/또는 생리학적으로 허용되는 이의 염을 약제에 삽입시킴을 특징으로 하여, 콜라겐 및 콜라겐-유사 물질의 생합성 및 Clq의 생합성에 영향을 끼치는 약제를 제조하는 방법.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019920001589A 1991-02-05 1992-02-01 2,4-및 2,5-비스테트라졸릴피리딘과 이의 제조방법 KR100214797B1 (ko)

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DEP4103372.8 1991-02-05
DE4103372 1991-02-05

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KR920016443A true KR920016443A (ko) 1992-09-24
KR100214797B1 KR100214797B1 (ko) 1999-08-02

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US (2) US5482953A (ko)
EP (1) EP0498334B1 (ko)
JP (1) JPH0559041A (ko)
KR (1) KR100214797B1 (ko)
AT (1) ATE193288T1 (ko)
AU (1) AU650511B2 (ko)
CA (1) CA2060622A1 (ko)
CZ (1) CZ283006B6 (ko)
DE (1) DE59209838D1 (ko)
DK (1) DK0498334T3 (ko)
ES (1) ES2146581T3 (ko)
FI (1) FI103117B1 (ko)
GR (1) GR3033536T3 (ko)
HR (1) HRP940840B1 (ko)
HU (1) HUT61295A (ko)
IE (1) IE920368A1 (ko)
IL (1) IL100860A (ko)
MX (1) MX9200492A (ko)
NO (1) NO180446C (ko)
NZ (1) NZ241505A (ko)
PT (1) PT498334E (ko)
YU (1) YU9492A (ko)
ZA (1) ZA92788B (ko)

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CZ305460B6 (cs) * 2013-05-06 2015-10-07 Contipro Biotech S.R.O. Způsob přípravy esteru 2-oxoglutarátu, přípravek obsahující ester 2-oxoglutarát a jeho použití

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3432094A1 (de) * 1984-08-31 1986-03-06 Hoechst Ag, 6230 Frankfurt Ester der pyridin-2,4- und -2,5- dicarbonsaeure als arzneimittel zur inhibierung der prolin- und lysinhydroxylase
DE3703962A1 (de) * 1987-02-10 1988-08-18 Hoechst Ag Pyridin-2,4- und 2,5-dicarbonsaeure-derivate, verfahren zu ihrer herstellung, verwendung derselben sowie arzneimittel auf basis dieser verbindungen
DE3703963A1 (de) * 1987-02-10 1988-08-18 Hoechst Ag Pyridin-2,4- und 2,,5-dicarbonsaeure-derivate, verfahren zu ihrer herstellung, verwendung derselben, sowie arzneimittel auf basis dieser verbindungen
US5238948A (en) * 1987-02-10 1993-08-24 Hoechst Aktiengesellschaft Pyridine-2,4- and -2,5-dicarboxylic acid derivatives and medicaments based on these compounds
DE3703959A1 (de) * 1987-02-10 1988-08-18 Hoechst Ag Pyridin-2,4- und 2,5-dicarbonsaeureamide, verfahren zu ihrer herstellung, verwendung derselben sowie arzneimittel auf basis dieser verbindungen
DE58908519D1 (de) * 1988-08-04 1994-11-24 Hoechst Ag Verbessertes Verfahren zur Herstellung von N,N-Bis(alkoxyalkyl)-pyridin -2,4-dicarbonsäurediamiden.
JPH02178263A (ja) * 1988-12-27 1990-07-11 Kaken Pharmaceut Co Ltd アザアズレン誘導体、その製造法およびそれを有効成分とする抗アレルギー剤および抗炎症剤
DE3924093A1 (de) * 1989-07-20 1991-02-07 Hoechst Ag N,n'-bis(alkoxy-alkyl)-pyridin-2,4-dicarbonsaeurediamide, verfahren zu deren herstellung sowie deren verwendung
FR2655801B1 (fr) * 1989-12-08 1992-03-13 Charbonnages De France Procede et dispositif de transmission de signaux video en milieu confine.
ZA91291B (en) * 1990-01-16 1991-09-25 Hoechst Ag Di(nitroxyalkyl)amides of pyridine-2,4-and-2,5-dicarboxylic acids,a process for the preparation thereof,and the use thereof
DE4020570A1 (de) * 1990-06-28 1992-01-02 Hoechst Ag 2,4- und 2,5-substituierte pyridin-n-oxide, verfahren zu deren herstellung sowie deren verwendung

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Publication number Publication date
GR3033536T3 (en) 2000-09-29
US5482953A (en) 1996-01-09
NO920462D0 (no) 1992-02-04
HUT61295A (en) 1992-12-28
HRP940840A2 (en) 1997-06-30
ATE193288T1 (de) 2000-06-15
EP0498334B1 (de) 2000-05-24
NO180446B (no) 1997-01-13
DK0498334T3 (da) 2000-09-18
EP0498334A1 (de) 1992-08-12
FI920460A (fi) 1992-08-06
FI103117B (fi) 1999-04-30
CZ283006B6 (cs) 1997-12-17
HU9200336D0 (en) 1992-04-28
FI103117B1 (fi) 1999-04-30
DE59209838D1 (de) 2000-06-29
MX9200492A (es) 1992-08-01
NZ241505A (en) 1994-12-22
NO920462L (no) 1992-08-06
AU650511B2 (en) 1994-06-23
AU1072492A (en) 1992-08-13
JPH0559041A (ja) 1993-03-09
KR100214797B1 (ko) 1999-08-02
PT498334E (pt) 2000-09-29
IE920368A1 (en) 1992-08-12
IL100860A (en) 1995-11-27
IL100860A0 (en) 1992-11-15
NO180446C (no) 1997-04-23
YU9492A (sh) 1995-03-27
ES2146581T3 (es) 2000-08-16
ZA92788B (en) 1992-10-28
FI920460A0 (fi) 1992-02-03
CA2060622A1 (en) 1992-08-06
HRP940840B1 (en) 2000-12-31
CS30992A3 (en) 1992-11-18
US5614537A (en) 1997-03-25

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