RU2001124567A - Производные индола и их применение в качестве антагонистов мср-1 - Google Patents

Производные индола и их применение в качестве антагонистов мср-1

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Publication number
RU2001124567A
RU2001124567A RU2001124567/04A RU2001124567A RU2001124567A RU 2001124567 A RU2001124567 A RU 2001124567A RU 2001124567/04 A RU2001124567/04 A RU 2001124567/04A RU 2001124567 A RU2001124567 A RU 2001124567A RU 2001124567 A RU2001124567 A RU 2001124567A
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Prior art keywords
compound according
chlorophenyl
compound
formula
ring
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RU2001124567/04A
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RU2235090C2 (ru
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Алан Веллингтон ФОЛЛ (GB)
Алан Веллингтон ФОЛЛ
Джейсон Грант КЕТТЛ (GB)
Джейсон Грант Кеттл
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Астразенека Аб (Se)
Астразенека Аб
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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
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/30Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
    • C07D209/42Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Indole Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Claims (10)

1. Соединение формулы (I)
Figure 00000001
в которой R1 представляет водород, галоген или метокси;
R2 представляет водород, галоген, метил, этил или метокси;
R3 представляет карбокси, тетразолил или -CONHSO2R4,
где R4 представляет метил, этил, фенил, 2,5-диметилизоксазолил или трифторметил;
Т представляет -СН2- или -SO2;
кольцо А представляет 3-хлорфенил, 4-хлорфенил, 3-трифторметилфенил, 3,4-дихлорфенил, 3,4-дифторфенил, 3-фтор-4-хлорфенил, 3-хлор-4-фторфенил или 2,3-дихлорпирид-5-ил;
или его фармацевтически приемлемая соль или пролекарство.
2. Соединение по п.1, в котором кольцо А представляет 3-хлорфенил, 4-хлорфенил, 3-трифторметилфенил, 3,4-дихлорфенил, 3,4-дифторфенил, 3-фтор-4-хлорфенил или 3-хлор-4-фторфенил.
3. Соединение по п.2, в котором кольцо А представляет 3,4-дихлорфенил, 3-фтор-4-хлорфенил или 3-хлор-4-фторфенил.
4. Соединение по п.1, в котором кольцо А представляет 3,4-дихлорфенил, 2,3-дихлорпирид-5-ил или 3-хлор-4-фторфенил.
5. Соединение по любому из предшествующих пунктов, в котором Т представляет -СН2-.
6. Соединение по любому из предшествующих пунктов, в котором R3 представляет карбоксигруппу.
7. Соединение по п.1, в котором в соединении формулы (I),
R1 представляет водород;
R2 представляет водород;
R3 представляет карбоксигруппу;
Т представляет -СН2-;
кольцо А представляет 3,4-дихлорфенил или 3-хлор-4-фторфенил;
или его фармацевтически приемлемая соль или пролекарство.
8. Способ получения соединения по п.1, причем включает:
а) реакцию соединений формулы (II)
Figure 00000002
в которой Ra представляет R3, определенную в п.1, или защищенную форму группы R3, Rb представляет водород или подходящую гидроксизащитную группу, а R1 и R2 представляют группы, определенные в п.1, с соединением формулы (III)
Figure 00000003
в которой Т и кольцо А имеют значения, определенные в п.1, a L представляет удаляемую группу;
и после этого при необходимости:
i) превращение соединения формулы (I) в другое соединение формулы (I),
ii) удаление любой защитной группы, или
iii) образование его фармацевтически приемлемой соли или пролекарства.
9. Фармацевтическая композиция, включающая соединение по любому из пп.1-7 в сочетании с фармацевтически приемлемым носителем.
10. Соединение по любому из пп.1-7 для применения при получении лекарственного средства для лечения заболевания, опосредованного моноцитарным хемоаттрактантным белком-1 или RANTES (регулируемый при активации, экспрессируемый и секретируемый нормальными Т-клетками), такого как воспалительное заболевание.
RU2001124567/04A 1999-02-05 2000-01-31 Производные индола и их применение в качестве антагонистов мср-1 RU2235090C2 (ru)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB9902461.4 1999-02-05
GBGB9902461.4A GB9902461D0 (en) 1999-02-05 1999-02-05 Chemical compounds

Publications (2)

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RU2235090C2 RU2235090C2 (ru) 2004-08-27

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EP (1) EP1150952B1 (ru)
JP (1) JP2002536359A (ru)
KR (1) KR20010094755A (ru)
CN (1) CN1339025A (ru)
AR (1) AR022461A1 (ru)
AT (1) ATE280757T1 (ru)
AU (1) AU770856B2 (ru)
BR (1) BR0007984A (ru)
CA (1) CA2356898A1 (ru)
CZ (1) CZ20012807A3 (ru)
DE (1) DE60015296T2 (ru)
EE (1) EE200100403A (ru)
GB (1) GB9902461D0 (ru)
HU (1) HUP0105079A3 (ru)
ID (1) ID30401A (ru)
IL (1) IL144611A0 (ru)
IS (1) IS5980A (ru)
MY (1) MY133209A (ru)
NO (1) NO20013809L (ru)
NZ (1) NZ512680A (ru)
PL (1) PL350184A1 (ru)
RU (1) RU2235090C2 (ru)
SK (1) SK11152001A3 (ru)
TR (1) TR200102233T2 (ru)
WO (1) WO2000046196A1 (ru)
ZA (1) ZA200105311B (ru)

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ZA200105311B (en) 2002-09-27
HUP0105079A3 (en) 2002-11-28
NO20013809L (no) 2001-10-02
SK11152001A3 (sk) 2001-12-03
NO20013809D0 (no) 2001-08-03
US6737435B1 (en) 2004-05-18
BR0007984A (pt) 2001-11-06
PL350184A1 (en) 2002-11-18
CZ20012807A3 (cs) 2001-10-17
CA2356898A1 (en) 2000-08-10
AU2121300A (en) 2000-08-25
EP1150952A1 (en) 2001-11-07
EP1150952B1 (en) 2004-10-27
KR20010094755A (ko) 2001-11-01
DE60015296D1 (de) 2004-12-02
IS5980A (is) 2001-06-26
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AU770856B2 (en) 2004-03-04
NZ512680A (en) 2003-11-28
IL144611A0 (en) 2002-05-23
JP2002536359A (ja) 2002-10-29
RU2235090C2 (ru) 2004-08-27
TR200102233T2 (tr) 2001-12-21
ATE280757T1 (de) 2004-11-15
CN1339025A (zh) 2002-03-06
HUP0105079A2 (hu) 2002-04-29
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AR022461A1 (es) 2002-09-04

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