CO4970719A1 - PIRROLOPYROLONE DERIVATIVES AS LEUCOCITARY ELASTASE INHIBITORS - Google Patents

PIRROLOPYROLONE DERIVATIVES AS LEUCOCITARY ELASTASE INHIBITORS

Info

Publication number
CO4970719A1
CO4970719A1 CO98051488A CO98051488A CO4970719A1 CO 4970719 A1 CO4970719 A1 CO 4970719A1 CO 98051488 A CO98051488 A CO 98051488A CO 98051488 A CO98051488 A CO 98051488A CO 4970719 A1 CO4970719 A1 CO 4970719A1
Authority
CO
Colombia
Prior art keywords
alkyl
carbon atoms
optionally substituted
halogen
groups
Prior art date
Application number
CO98051488A
Other languages
Spanish (es)
Inventor
Geoffrey Duke Edward Clarke
Original Assignee
Glaxo Group Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from GBGB9719183.7A external-priority patent/GB9719183D0/en
Priority claimed from GBGB9719189.4A external-priority patent/GB9719189D0/en
Priority claimed from GBGB9719290.0A external-priority patent/GB9719290D0/en
Priority claimed from GBGB9803611.4A external-priority patent/GB9803611D0/en
Application filed by Glaxo Group Ltd filed Critical Glaxo Group Ltd
Publication of CO4970719A1 publication Critical patent/CO4970719A1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/02Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pulmonology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Dermatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Hydrogenated Pyridines (AREA)

Abstract

Un compuesto de la fórmula (I)(estereoquímica relativa indicada)en donde: R1 representa alquilo de 1 a 6 átomos de carbono; R2 representa alquilo de 2 a 4 átomos de carbono o alquenilo de 2 a 4 átomos de carbono; X representa CO o SO2 ; Het representa un sistema de anillo aromáticomonocíclico o bicíclico de 5 a 10 elementos, opcionalmente substituido, que contiene 1 a 4 heteroátomos seleccionados de O, N, y S; n representa un número entero de 0 a 4; R3 y R4 representan independientemente hidrógeno, alquilo de 1 a 8 átomos de carbono, -(CH2 )1-4 CONR5 R6 , COC1-4 alquilo o(CH2 )0-2 Fen en donde Fen representa fenilo opcionalmente sustituido por uno o más grupos alquilo de 1 a 4 átomos de carbono o grupos halógeno o NR3 R4 juntos representan azetidinilo, pirrolidinilo, piperidinilo, azepinilo, morfolinilo, piperazinilo opcionalmente N-susbtituido por alquilo de 1 a 6 átomos de carbono, fenilo(opcionalmente substituido por halógeno o alquilo de 1 a 4 átomos de carbono) o bencilo (opcionalmente substituido en el anillo de benceno por halógeno o alquilo de 1 a 4 átomos de carbono) o NR3 R4 juntos representan un anillo como se ha descrito hasta ahora salvo que se substituye en el carbono por uno o más grupos alquilo de 1 a 4 átomos de carbono, CONR5 R6 o COOR6 . R5 y R6 representan independientemente hidrógeno o alquilo de 1 a 4 átomos de carbono; y sales y solvatos de los mismos.A compound of formula (I) (indicated relative stereochemistry) wherein: R1 represents alkyl of 1 to 6 carbon atoms; R2 represents alkyl of 2 to 4 carbon atoms or alkenyl of 2 to 4 carbon atoms; X represents CO or SO2; Het represents an optionally substituted 5 to 10 membered bicyclic or bicyclic aromatic ring system containing 1 to 4 heteroatoms selected from O, N, and S; n represents an integer from 0 to 4; R3 and R4 independently represent hydrogen, alkyl of 1 to 8 carbon atoms, - (CH2) 1-4 CONR5 R6, COC1-4 alkyl or (CH2) 0-2 Fen where Fen represents phenyl optionally substituted by one or more groups C 1-4 -alkyl or halogen groups or NR3 R4 together represent azetidinyl, pyrrolidinyl, piperidinyl, azepinyl, morpholinyl, piperazinyl optionally N-substituted by C 1-6 -alkyl, phenyl (optionally substituted by halogen or alkyl of 1 to 4 carbon atoms) or benzyl (optionally substituted on the benzene ring by halogen or alkyl of 1 to 4 carbon atoms) or NR3 R4 together represent a ring as described so far except that it is substituted on carbon by one or more alkyl groups of 1 to 4 carbon atoms, CONR5 R6 or COOR6. R5 and R6 independently represent hydrogen or C1-C4-alkyl; and salts and solvates thereof.

CO98051488A 1997-09-09 1998-09-08 PIRROLOPYROLONE DERIVATIVES AS LEUCOCITARY ELASTASE INHIBITORS CO4970719A1 (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
GBGB9719183.7A GB9719183D0 (en) 1997-09-09 1997-09-09 Compounds
GBGB9719189.4A GB9719189D0 (en) 1997-09-09 1997-09-09 New therapeutic method
GBGB9719290.0A GB9719290D0 (en) 1997-09-10 1997-09-10 Compounds
GBGB9803611.4A GB9803611D0 (en) 1998-02-21 1998-02-21 Compounds

Publications (1)

Publication Number Publication Date
CO4970719A1 true CO4970719A1 (en) 2000-11-07

Family

ID=27451698

Family Applications (1)

Application Number Title Priority Date Filing Date
CO98051488A CO4970719A1 (en) 1997-09-09 1998-09-08 PIRROLOPYROLONE DERIVATIVES AS LEUCOCITARY ELASTASE INHIBITORS

Country Status (24)

Country Link
EP (1) EP1003748A2 (en)
JP (1) JP2001515904A (en)
KR (1) KR20010023766A (en)
CN (1) CN1278820A (en)
AP (1) AP2000001761A0 (en)
AR (1) AR017072A1 (en)
AU (1) AU9741298A (en)
BR (1) BR9812062A (en)
CA (1) CA2303176A1 (en)
CO (1) CO4970719A1 (en)
EA (1) EA200000204A1 (en)
EE (1) EE200000138A (en)
HU (1) HUP0004644A3 (en)
ID (1) ID24452A (en)
IL (1) IL134791A0 (en)
IS (1) IS5391A (en)
MA (1) MA26543A1 (en)
NO (1) NO20001198L (en)
NZ (1) NZ503130A (en)
PE (1) PE107899A1 (en)
PL (1) PL339176A1 (en)
SK (1) SK3192000A3 (en)
TR (1) TR200000907T2 (en)
WO (1) WO1999012933A2 (en)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9905418D0 (en) * 1999-03-09 1999-05-05 Glaxo Group Ltd Process
MXPA06011410A (en) 2004-03-31 2007-04-20 Johnson & Johnson Non-imidazole heterocyclic compounds.
DE102004024772A1 (en) * 2004-05-17 2005-12-22 Grünenthal GmbH Substituted 5-aminomethyl-1H-pyrrole-2-carboxamides
JP4853759B2 (en) * 2004-05-27 2012-01-11 日本農薬株式会社 Substituted pyrazinecarboxylic acid anilide derivatives or salts thereof, intermediates thereof, agricultural and horticultural agents, and methods of use thereof
TWI355380B (en) * 2004-05-27 2012-01-01 Nihon Nohyaku Co Ltd Substituted pyrazinecarboxanilide derivatives or s
GB2418427A (en) 2004-09-02 2006-03-29 Univ Cambridge Tech Ligands for G-protein coupled receptors
KR20070084455A (en) 2004-11-23 2007-08-24 워너-램버트 캄파니 엘엘씨 7-(2h-pyrazol-3-yl)-3,5-dihydroxy-heptanoic acid derivatives as hmg co-a reductase inhibitors for the treatment of lipidemia
NZ572250A (en) 2006-05-04 2011-10-28 Pulmagen Therapeutics Inflammation Ltd Tetrahydropyrrolopyrimidinediones and their use as human neutrophil elastase inhibitors
US8198288B2 (en) 2006-05-04 2012-06-12 Pulmagen Therapeutics (Inflammation) Limited Tetrahydropyrrolopyrimidinediones and their use in therapy
US7662967B2 (en) 2007-08-02 2010-02-16 Cambridge Enterprise Limited Anti-inflammatory compounds and compositions
GB2452696B (en) 2007-08-02 2009-09-23 Cambridge Entpr Ltd 3-(2',2'-dimethylpropanoylamino)-tetrahydropyridin-2-one and its use in pharmaceutical compositions
WO2009060206A1 (en) * 2007-11-07 2009-05-14 Argenta Discovery Limited 3,4,6,7-tetrahydro-1h-pyrrolo[3,4-d]pyrimidine-2,5-diones and their therapeutic use
US20110212181A1 (en) * 2010-02-26 2011-09-01 The University Of Hong Kong Compositions and methods for treating chronic respiratory inflammation
BR112022004861A2 (en) 2019-09-17 2022-06-07 Univ Duke Alvestat for use in the treatment of transplant rejection, bronchiolitis obliterans syndrome and transplant versus host disease
IL297211A (en) 2020-04-16 2022-12-01 Mereo Biopharma 4 Ltd Methods involving neutrophil elastase inhibitor alvelestat for treating respiratory disease mediated by alpha-1 antitrypsin deficiency
TW202325294A (en) 2021-10-20 2023-07-01 英商梅瑞奧生物製藥4有限公司 Neutrophil elastase inhibitors for use in the treatment of fibrosis

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9211783D0 (en) * 1992-06-04 1992-07-15 Ici Plc Amide derivatives
GB9402680D0 (en) * 1994-02-11 1994-04-06 Zeneca Ltd Pyrrolidine derivatives
ES2217404T3 (en) * 1996-03-28 2004-11-01 Glaxo Group Limited PIRROLOPIRROLONE DERIVATIVES AS INHIBITORS OF THE ELASTASA DE NEUTROFILOS.

Also Published As

Publication number Publication date
AP2000001761A0 (en) 2000-03-31
EA200000204A1 (en) 2000-10-30
BR9812062A (en) 2000-09-26
CN1278820A (en) 2001-01-03
AU9741298A (en) 1999-03-29
NO20001198D0 (en) 2000-03-08
WO1999012933A2 (en) 1999-03-18
JP2001515904A (en) 2001-09-25
AR017072A1 (en) 2001-08-22
HUP0004644A3 (en) 2002-01-28
IS5391A (en) 2000-02-29
NO20001198L (en) 2000-05-08
SK3192000A3 (en) 2001-03-12
WO1999012933A3 (en) 1999-05-27
TR200000907T2 (en) 2000-11-21
EP1003748A2 (en) 2000-05-31
IL134791A0 (en) 2001-04-30
HUP0004644A2 (en) 2001-09-28
NZ503130A (en) 2001-08-31
CA2303176A1 (en) 1999-03-18
KR20010023766A (en) 2001-03-26
EE200000138A (en) 2001-02-15
PL339176A1 (en) 2000-12-04
MA26543A1 (en) 2004-12-20
PE107899A1 (en) 1999-11-17
ID24452A (en) 2000-07-20

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