HUP0001389A2 - Pyrazolopyrimidinones, process for their preparation, use thereof, pharmaceutical compositions containing them - Google Patents

Pyrazolopyrimidinones, process for their preparation, use thereof, pharmaceutical compositions containing them

Info

Publication number
HUP0001389A2
HUP0001389A2 HU0001389A HUP0001389A HUP0001389A2 HU P0001389 A2 HUP0001389 A2 HU P0001389A2 HU 0001389 A HU0001389 A HU 0001389A HU P0001389 A HUP0001389 A HU P0001389A HU P0001389 A2 HUP0001389 A2 HU P0001389A2
Authority
HU
Hungary
Prior art keywords
alkyl
alkoxy
optionally substituted
piperazinyl
linked
Prior art date
Application number
HU0001389A
Other languages
Hungarian (hu)
Inventor
Mark Edward Bunnage
John Paul Mathias
Stephen Derek Albert Street
Anthony Wood
Original Assignee
Pfizer Inc.
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
Application filed by Pfizer Inc. filed Critical Pfizer Inc.
Priority claimed from PCT/EP1998/002257 external-priority patent/WO1998049166A1/en
Publication of HUP0001389A2 publication Critical patent/HUP0001389A2/en
Publication of HUP0001389A3 publication Critical patent/HUP0001389A3/en

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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

Pyrazolo (4,3-d) pyrimidin-7-ones of formula (I) and their salts and solvates are new. Ring A is of formula (a) or (b); R1 = 1-3C alkyl substituted by 3-6C cycloalkyl, CONR5R6 or N-linked heterocycle selected from pyrazolyl, imidazolyl, triazolyl, pyrrolidinyl, piperidinyl, morpholinyl and 4-R9-piperazinyl; (CH2)nHet; or (CH2)nAr; R2 = 1-6C alkyl; R3 = 1-6C alkyl (optionally substituted by alkoxy); R4 = SO2NR7R8; R5, R6 = H or alkyl (optionally substituted by alkoxy); or NR5R6 = pyrrolidinyl, piperidinyl, morpholinyl or 4-R9-piperazinyl; NR7R8 = 4-R10-piperazinyl; R9 = alkyl; R10 = H or alkyl (optionally substituted by OH, alkoxy or CONH2); Het = C-linked 6-membered heterocycle containing 1 or 2 N (optionally as a mono-N-oxide) or C-linked 5-membered heterocycle containing 1-4 heteroatoms selected from N, O and S, both optionally substituted by 1 or 2 of alkyl (optionally substituted by alkoxy), alkoxy, halo and NH2; Ar = phenyl (optionally substituted by 1 or 2 of alkyl, alkoxy, halo, CN, CONH2, NO2, NH2, NHSO2- alkyl and SO2NH2); n = 0 to 1; alkyl moieties have 1-4C unless specified otherwise.
HU0001389A 1997-10-30 1998-04-10 Pyrazolopyrimidinones, process for their preparation, use thereof, pharmaceutical compositions containing them HUP0001389A3 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB9722954.6A GB9722954D0 (en) 1997-10-30 1997-10-30 Therapeutic agents
PCT/EP1998/002257 WO1998049166A1 (en) 1997-04-25 1998-04-10 PYRAZOLOPYRIMIDINONES WHICH INHIBIT TYPE 5 CYCLIC GUANOSINE 3',5'-MONOPHOSPHATE PHOSPHODIESTERASE (cGMP PDE5) FOR THE TREATMENT OF SEXUAL DYSFUNCTION

Publications (2)

Publication Number Publication Date
HUP0001389A2 true HUP0001389A2 (en) 2000-09-28
HUP0001389A3 HUP0001389A3 (en) 2001-04-28

Family

ID=10821332

Family Applications (1)

Application Number Title Priority Date Filing Date
HU0001389A HUP0001389A3 (en) 1997-10-30 1998-04-10 Pyrazolopyrimidinones, process for their preparation, use thereof, pharmaceutical compositions containing them

Country Status (2)

Country Link
GB (1) GB9722954D0 (en)
HU (1) HUP0001389A3 (en)

Also Published As

Publication number Publication date
HUP0001389A3 (en) 2001-04-28
GB9722954D0 (en) 1998-01-07

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Legal Events

Date Code Title Description
FA9A Lapse of provisional patent protection due to relinquishment or protection considered relinquished