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BE902150A - 1H, 7H-PYRAZOLO (1,5-A) PYRIMIDINE-7-ONE DERIVATIVES AND PROCESS FOR THEIR PREPARATION. - Google Patents

1H, 7H-PYRAZOLO (1,5-A) PYRIMIDINE-7-ONE DERIVATIVES AND PROCESS FOR THEIR PREPARATION.

Info

Publication number
BE902150A
BE902150A BE0/214812A BE214812A BE902150A BE 902150 A BE902150 A BE 902150A BE 0/214812 A BE0/214812 A BE 0/214812A BE 214812 A BE214812 A BE 214812A BE 902150 A BE902150 A BE 902150A
Authority
BE
Belgium
Prior art keywords
compounds
optionally substituted
pyrazolo
pyrimidine
derivatives
Prior art date
Application number
BE0/214812A
Other languages
French (fr)
Inventor
G Doria
C Passarotti
R Sala
A Rossi
Original Assignee
Erba Farmitalia
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 Erba Farmitalia filed Critical Erba Farmitalia
Publication of BE902150A publication Critical patent/BE902150A/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
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/08Antiepileptics; Anticonvulsants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/20Hypnotics; Sedatives

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Anesthesiology (AREA)
  • Pain & Pain Management (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

Composés de la formule (I) ou R1 est un groupe alkyle en C1-C6, benzyle, pyridyle où phényle, ces deux derniers éventuellement substitués, R2 représente un radical pyridyle ou phényle éventuellement substitué, R3 représente un atome d'hydrogène ou radical alkyle en C1-C6 éventuellement substitué, R4 représente un hydrogène, un halogène, un radical alkyle en C1-C6, hydroxyle, alcoxy en C1-C6, alcényloxy en C3-C4, formyloxy ou alcanoyloxy en C2-C6, ainsi que les sels pharmaceutiquement acceptables de ces composés. Ces composés sont destinés à etre utilisés en tant que dépresseurs du système nerveux central.Compounds of formula (I) where R1 is a C1-C6 alkyl group, benzyl, pyridyl or phenyl, these latter two optionally substituted, R2 represents a pyridyl or optionally substituted phenyl radical, R3 represents a hydrogen atom or an alkyl radical in C1-C6 optionally substituted, R4 represents a hydrogen, a halogen, a C1-C6 alkyl radical, hydroxyl, C1-C6 alkoxy, C3-C4 alkenyloxy, formyloxy or C2-C6 alkanoyloxy, as well as the pharmaceutically salts acceptable of these compounds. These compounds are intended to be used as depressants of the central nervous system.

BE0/214812A 1984-04-11 1985-04-10 1H, 7H-PYRAZOLO (1,5-A) PYRIMIDINE-7-ONE DERIVATIVES AND PROCESS FOR THEIR PREPARATION. BE902150A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB08409424A GB2157285B (en) 1984-04-11 1984-04-11 1h, 7h-pyrazolo1, 5-a pyrimidine-7-one derivatives and process for their preparation

Publications (1)

Publication Number Publication Date
BE902150A true BE902150A (en) 1985-07-31

Family

ID=10559537

Family Applications (1)

Application Number Title Priority Date Filing Date
BE0/214812A BE902150A (en) 1984-04-11 1985-04-10 1H, 7H-PYRAZOLO (1,5-A) PYRIMIDINE-7-ONE DERIVATIVES AND PROCESS FOR THEIR PREPARATION.

Country Status (4)

Country Link
JP (1) JPS60228483A (en)
BE (1) BE902150A (en)
DE (1) DE3510134A1 (en)
GB (1) GB2157285B (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2812636A1 (en) * 2000-08-02 2002-02-08 Novapharme New imidazo (1,2-a) pyrimidin-5(1H)-one derivatives, useful as general anesthetics and sedatives having rapid action and short plasma half life
ES2276936T3 (en) 2001-03-27 2007-07-01 Neurogen Corporation (OXO-PIRAZOLO (1,5A) PIRIMIDIN-2-IL) ALQUILCARBOXAMIDAS.
JP4895220B2 (en) 2004-04-06 2012-03-14 ノバルティス バクシンズ アンド ダイアグノスティックス,インコーポレーテッド Kinesin Mitosis Inhibitor
CA2674318A1 (en) 2007-01-05 2008-07-17 Novartis Ag Cyclized derivatives as eg-5 inhibitors

Also Published As

Publication number Publication date
GB2157285B (en) 1987-10-28
GB8409424D0 (en) 1984-05-23
JPS60228483A (en) 1985-11-13
GB2157285A (en) 1985-10-23
DE3510134A1 (en) 1985-10-24

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Legal Events

Date Code Title Description
RE Patent lapsed

Owner name: FARMITALIA CARLO ERBA S.P.A.

Effective date: 19880430