Pyrazolo[3,4-b]pyridine compounds, and their use as phosphodiesterase inhibitors

Abstract The invention relates to a compound of formula (I) or a salt thereof: Formula (I) wherein: R1 is C .4alkyl, C1.3fluoroalkyl or -(CH 2)20H; R2 is a hydrogen atom (H), methyl or Cifluoroalkyl; R3a is a hydrogen atom (H) or C1.3alkyl; R3 is optionally substituted 5 branched C3 .6 alkyl, option...

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Main Authors COOK, CAROLINE MARY, JOHNSON, MARTIN REDPATH, COOPER, ANTHONY WILLIAM JAMES, ALLEN, DAVID GEORGE, MITCHELL, CHARLOTTE JANE, HAMBLIN, JULIE NICOLE, REDGRAVE, ALISON JUDITH, EDLIN, CHRISTOPHER DAVID, COE, DIANE MARY, LINDVALL, MIKA KRISTIAN, DOWLE, MICHAEL DENNIS, JONES, PAUL SPENCER
Format Patent
LanguageEnglish
Published 30.08.2012
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Abstract Abstract The invention relates to a compound of formula (I) or a salt thereof: Formula (I) wherein: R1 is C .4alkyl, C1.3fluoroalkyl or -(CH 2)20H; R2 is a hydrogen atom (H), methyl or Cifluoroalkyl; R3a is a hydrogen atom (H) or C1.3alkyl; R3 is optionally substituted 5 branched C3 .6 alkyl, optionally substituted C3.scycloalkyl, optionally substituted mono unsaturated-C 5.7cycloalkenyl, optionally substituted phenyl, or an optionally substituted heterocyclic group of sub-formula (aa), or (bb) or (cc) in which nI and n2 independently are I or 2; and Y is 0, S, SO 2 , or NR4, and wherein Het is of sub-formula (i), or (ii), or (iii), or (iv) or (v). The compounds are phosphodiesterase (PDE) inhibitors, in particular 10 PDE4 inhibitors. Also provided is the use of a compound of formula (I), or a pharmaceutically acceptable salt thereof, in the manufacture of a medicament for the treatment and/or prophylaxis of an inflammatory and/or allergic disease in a mammal such as a human, for example chronic obstructive pulmonary disease (COPD), asthma, or allergic rhinitis.
AbstractList Abstract The invention relates to a compound of formula (I) or a salt thereof: Formula (I) wherein: R1 is C .4alkyl, C1.3fluoroalkyl or -(CH 2)20H; R2 is a hydrogen atom (H), methyl or Cifluoroalkyl; R3a is a hydrogen atom (H) or C1.3alkyl; R3 is optionally substituted 5 branched C3 .6 alkyl, optionally substituted C3.scycloalkyl, optionally substituted mono unsaturated-C 5.7cycloalkenyl, optionally substituted phenyl, or an optionally substituted heterocyclic group of sub-formula (aa), or (bb) or (cc) in which nI and n2 independently are I or 2; and Y is 0, S, SO 2 , or NR4, and wherein Het is of sub-formula (i), or (ii), or (iii), or (iv) or (v). The compounds are phosphodiesterase (PDE) inhibitors, in particular 10 PDE4 inhibitors. Also provided is the use of a compound of formula (I), or a pharmaceutically acceptable salt thereof, in the manufacture of a medicament for the treatment and/or prophylaxis of an inflammatory and/or allergic disease in a mammal such as a human, for example chronic obstructive pulmonary disease (COPD), asthma, or allergic rhinitis.
Author HAMBLIN, JULIE NICOLE
LINDVALL, MIKA KRISTIAN
ALLEN, DAVID GEORGE
REDGRAVE, ALISON JUDITH
COOK, CAROLINE MARY
EDLIN, CHRISTOPHER DAVID
DOWLE, MICHAEL DENNIS
JOHNSON, MARTIN REDPATH
MITCHELL, CHARLOTTE JANE
COOPER, ANTHONY WILLIAM JAMES
COE, DIANE MARY
JONES, PAUL SPENCER
Author_xml – fullname: COOK, CAROLINE MARY
– fullname: JOHNSON, MARTIN REDPATH
– fullname: COOPER, ANTHONY WILLIAM JAMES
– fullname: ALLEN, DAVID GEORGE
– fullname: MITCHELL, CHARLOTTE JANE
– fullname: HAMBLIN, JULIE NICOLE
– fullname: REDGRAVE, ALISON JUDITH
– fullname: EDLIN, CHRISTOPHER DAVID
– fullname: COE, DIANE MARY
– fullname: LINDVALL, MIKA KRISTIAN
– fullname: DOWLE, MICHAEL DENNIS
– fullname: JONES, PAUL SPENCER
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Snippet Abstract The invention relates to a compound of formula (I) or a salt thereof: Formula (I) wherein: R1 is C .4alkyl, C1.3fluoroalkyl or -(CH 2)20H; R2 is a...
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SubjectTerms CHEMISTRY
HETEROCYCLIC COMPOUNDS
HUMAN NECESSITIES
HYGIENE
MEDICAL OR VETERINARY SCIENCE
METALLURGY
ORGANIC CHEMISTRY
PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS
Title Pyrazolo[3,4-b]pyridine compounds, and their use as phosphodiesterase inhibitors
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