IT1183483B - Derivati di 1-fluorofenilbutil-4-(2-pirimidinil)fiperazina antipsicotici - Google Patents

Derivati di 1-fluorofenilbutil-4-(2-pirimidinil)fiperazina antipsicotici

Info

Publication number
IT1183483B
IT1183483B IT19773/85A IT1977385A IT1183483B IT 1183483 B IT1183483 B IT 1183483B IT 19773/85 A IT19773/85 A IT 19773/85A IT 1977385 A IT1977385 A IT 1977385A IT 1183483 B IT1183483 B IT 1183483B
Authority
IT
Italy
Prior art keywords
fluorofenilbutil
fiperazine
antipsychotics
pyrimidinyl
derivatives
Prior art date
Application number
IT19773/85A
Other languages
English (en)
Italian (it)
Other versions
IT8519773A0 (it
Inventor
Joseph P Ywvich
Walter G Lobeck Jr
Original Assignee
Bristol Myers Co
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 Bristol Myers Co filed Critical Bristol Myers Co
Publication of IT8519773A0 publication Critical patent/IT8519773A0/it
Application granted granted Critical
Publication of IT1183483B publication Critical patent/IT1183483B/it

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
    • C07D317/10—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings
    • C07D317/12—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/32—One oxygen, sulfur or nitrogen atom
    • C07D239/42—One nitrogen atom
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Neurology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Biomedical Technology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Psychiatry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Neurosurgery (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Legs For Furniture In General (AREA)
IT19773/85A 1984-03-06 1985-03-05 Derivati di 1-fluorofenilbutil-4-(2-pirimidinil)fiperazina antipsicotici IT1183483B (it)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US58658084A 1984-03-06 1984-03-06
US06/683,309 US4605655A (en) 1984-03-06 1984-12-18 Antipsychotic 1-fluorophenylbutyl-4-(2-pyrimidinyl)piperazine derivatives

Publications (2)

Publication Number Publication Date
IT8519773A0 IT8519773A0 (it) 1985-03-05
IT1183483B true IT1183483B (it) 1987-10-22

Family

ID=27079753

Family Applications (1)

Application Number Title Priority Date Filing Date
IT19773/85A IT1183483B (it) 1984-03-06 1985-03-05 Derivati di 1-fluorofenilbutil-4-(2-pirimidinil)fiperazina antipsicotici

Country Status (27)

Country Link
US (1) US4605655A (en:Method)
KR (3) KR920005113B1 (en:Method)
AT (1) AT390951B (en:Method)
AU (1) AU576555B2 (en:Method)
BE (1) BE901880A (en:Method)
CA (1) CA1256871A (en:Method)
CH (1) CH663022A5 (en:Method)
CY (1) CY1545A (en:Method)
DE (1) DE3507983A1 (en:Method)
DK (1) DK166149C (en:Method)
ES (1) ES8607254A1 (en:Method)
FI (1) FI84478C (en:Method)
FR (1) FR2560878B1 (en:Method)
GB (1) GB2155925B (en:Method)
GR (1) GR850561B (en:Method)
HK (1) HK82890A (en:Method)
HU (1) HU193949B (en:Method)
IE (1) IE58338B1 (en:Method)
IT (1) IT1183483B (en:Method)
LU (1) LU85796A1 (en:Method)
MX (1) MX9203177A (en:Method)
MY (1) MY102240A (en:Method)
NL (1) NL8500628A (en:Method)
PT (1) PT80058B (en:Method)
SE (1) SE462429B (en:Method)
SG (1) SG35590G (en:Method)
ZA (1) ZA851486B (en:Method)

Families Citing this family (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4668687A (en) * 1984-07-23 1987-05-26 Bristol-Myers Company Psychogeriatric 1-(2-pyrimidinyl)piperazinyl derivatives of 1-pyrrolidin-2-ones
US4677104A (en) * 1985-05-06 1987-06-30 Bristol-Myers Company Antipsychotic fused-ring pyridinylpiperazine derivatives
US4766215A (en) * 1987-02-27 1988-08-23 American Home Products Corporation Histamine H1 -receptor antagonists
SE8701375D0 (sv) * 1987-04-02 1987-04-02 Leo Ab Novel pyridyl- and pyrimidyl derivatives
US4826844A (en) * 1987-09-30 1989-05-02 American Home Products Corporation Substituted 1-(aralkyl-piperazinoalkyl) cycloalkanols
US4994455A (en) * 1987-10-26 1991-02-19 Pfizer Inc. Anti-anxiety agents
US4882432A (en) * 1989-01-09 1989-11-21 American Home Products Corporation Polycyclic-carbamic acid piperazinoalkyl esters and amides
GB8909209D0 (en) * 1989-04-22 1989-06-07 Wyeth John & Brother Ltd Piperazine derivatives
DE69033393T2 (de) * 1989-04-22 2000-05-25 American Home Products Corp., Madison Tertiäre alkyl funktionalisierte Piperazin-Derivate
US4994460A (en) * 1989-06-01 1991-02-19 Bristol-Myers Squibb Co. Agents for treatment of brain ischemia
US5055470A (en) * 1989-06-01 1991-10-08 Bristol-Myers Squibb Co. Method of treatment of ischemia in brain
FR2672052B1 (fr) * 1991-01-28 1995-05-24 Esteve Labor Dr Derives d'aryl (ou heteroaryl)-piperazinyl-alkyl-azoles, leur preparation et leur application en tant que medicaments.
US5681956A (en) * 1990-12-28 1997-10-28 Neurogen Corporation 4-aryl substituted piperazinylmethyl phenylimidazole derivatives; a new class of dopamine receptor subtype specific ligands
US5633377A (en) * 1990-12-28 1997-05-27 Neurogen Corporation 4-piperidino- and piperazinomethyl-2-cyclohexyl imidazole derivatives; dopamine receptor subtype specific ligands
US5512584A (en) * 1991-04-16 1996-04-30 Basf Aktiengesellschaft 1,3,4-trisubstituted piperidine derivatives, the preparation and use thereof
EP0538693A3 (en) * 1991-10-23 1994-08-17 Squibb & Sons Inc Stereoselective preparation of halophenyl alcohols
IL103499A0 (en) * 1991-10-24 1993-03-15 Bristol Myers Squibb Co Pharmaceutical compositions for treating anxiety in benzodiazepine withdrawn patients
SE9201239D0 (sv) * 1992-04-21 1992-04-21 Kabi Pharmacia Ab Agents for treating substance abuse disorders
US5324662A (en) * 1992-05-15 1994-06-28 E. R. Squibb & Sons, Inc. Stereoselective microbial or enzymatic reduction of 3,5-dioxo esters to 3-hydroxy-5-oxo, 3-oxo-5-hydroxy, and 3,5-dihydroxy esters
DE4219973A1 (de) * 1992-06-19 1993-12-23 Basf Ag N-substituierte Azabicycloheptan-Derivate, ihre Herstellung und Verwendung
DE4243287A1 (de) * 1992-06-19 1993-12-23 Basf Ag N-Substituierte Azabicycloheptan-Derivate, ihre Herstellung und Verwendung
RU2124511C1 (ru) * 1993-05-14 1999-01-10 Фармасьютикал Ко., Лтд Производные пиперазина
ES2074946B1 (es) * 1993-07-19 1996-06-16 Ferrer Int Nuevos compuestos derivados de la 1,2-etanodiamina-n,n,n',n'-tetrasustituida.
DE4341403A1 (de) * 1993-12-04 1995-06-08 Basf Ag N-substituierte 3-Azabicycloalkan-Derivate, ihre Herstellung und Verwendung
CA2187542C (en) * 1994-04-18 2000-02-01 Nobuyuki Takahashi Adamantane derivative, process for producing the same, and use thereof
US5607936A (en) * 1994-09-30 1997-03-04 Merck & Co., Inc. Substituted aryl piperazines as neurokinin antagonists
ES2104509B1 (es) * 1995-06-13 1998-07-01 Ferrer Int Nuevos compuestos derivados de 2-(3,4-disustituido-1-piperazinil)-5-fluoropirimidina.
US6166205A (en) * 1998-09-02 2000-12-26 Neurogen Corporation 2-Aryl-4-(1-[4-heteroaryl]piperazin-1-yl)methylimidazoles: dopamine . D.sub4 receptor subtype ligands
CA2686547C (en) * 2007-05-14 2015-12-08 Sk Holdings Co., Ltd. Novel carbamoyloxy aryl alkan arylpiperazine compound, pharmaceutical compositions comprising the compound and method for treating pain, anxiety and depression by administering the compound
EP3610890A1 (en) 2012-11-14 2020-02-19 The Johns Hopkins University Methods and compositions for treating schizophrenia
WO2021236879A1 (en) 2020-05-20 2021-11-25 The Board Of Trustees Of The University Of Illinois Method for treating lysosomal storage diseases with histatin peptides

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL127061C (en:Method) * 1959-03-26
US2979508A (en) * 1959-10-12 1961-04-11 Paul A J Janssen Heterocyclic derivatives of 1-phenyl-omega-(piperazine) alkanols
US2985657A (en) * 1959-10-12 1961-05-23 Paul A J Janssen 1-(aroylalkyl)-4-heterocyclylpiperazines
US2973360A (en) * 1959-10-12 1961-02-28 Paul A J Janssen Certain 1-(2-theonyl lower alkyl)-4-(heterocyclic substituted)-piperazines
NL127996C (en:Method) * 1963-11-19
GB1259685A (en) * 1969-04-03 1972-01-12 Soc D Etudes Prod Chimique Amino-pyrimidine derivatives
BE758380A (fr) * 1969-11-04 1971-04-16 Sumitomo Chemical Co Procede de preparation de derives d'aryl-cetones
GB1307256A (en) * 1970-09-15 1973-02-14 Science Union & Cie Piperazine derivatives and a process for their preparation
BE882836A (fr) * 1979-05-15 1980-08-18 Soc D Etudes Prod Chimique Nouveaux derives halogenes de l'isopropylamino pyrimidine, leur preparation et leur utilisaton therapeutique
US4316899A (en) * 1979-08-24 1982-02-23 Beecham Group Limited Chromanone derivatives, a process for their preparation and compositions containing them
DE3321969A1 (de) * 1983-06-18 1984-12-20 Troponwerke GmbH & Co KG, 5000 Köln 2-pyrimidinyl-1-piperazin-derivate, verfahren zu ihrer herstellung und diese enthaltende arzneimittel

Also Published As

Publication number Publication date
DE3507983A1 (de) 1985-09-12
IE850546L (en) 1985-09-06
KR920005113B1 (ko) 1992-06-26
GR850561B (en:Method) 1985-07-03
GB8505662D0 (en) 1985-04-03
DK166149C (da) 1993-08-09
FI850850L (fi) 1985-09-07
KR920005114B1 (ko) 1992-06-26
US4605655A (en) 1986-08-12
DK100685D0 (da) 1985-03-05
SE462429B (sv) 1990-06-25
CH663022A5 (de) 1987-11-13
HU193949B (en) 1987-12-28
HK82890A (en) 1990-10-19
FR2560878A1 (fr) 1985-09-13
KR850006402A (ko) 1985-10-05
DK166149B (da) 1993-03-15
ES8607254A1 (es) 1986-05-16
GB2155925B (en) 1987-11-25
NL8500628A (nl) 1985-10-01
AU576555B2 (en) 1988-09-01
ATA64985A (de) 1990-01-15
AU3944985A (en) 1985-09-12
MY102240A (en) 1992-05-15
BE901880A (fr) 1985-09-05
DK100685A (da) 1985-09-07
GB2155925A (en) 1985-10-02
SE8501067L (sv) 1985-09-07
FR2560878B1 (fr) 1988-10-14
AT390951B (de) 1990-07-25
CY1545A (en) 1991-03-22
PT80058B (pt) 1987-10-20
SG35590G (en) 1990-07-13
ES540901A0 (es) 1986-05-16
CA1256871A (en) 1989-07-04
SE8501067D0 (sv) 1985-03-05
IE58338B1 (en) 1993-09-08
LU85796A1 (fr) 1985-12-12
FI84478C (fi) 1991-12-10
HUT37781A (en) 1986-02-28
KR920005694B1 (ko) 1992-07-13
ZA851486B (en) 1985-11-27
IT8519773A0 (it) 1985-03-05
MX9203177A (es) 1992-07-01
FI850850A0 (fi) 1985-03-01
FI84478B (fi) 1991-08-30
PT80058A (en) 1985-04-01

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Legal Events

Date Code Title Description
TA Fee payment date (situation as of event date), data collected since 19931001

Effective date: 19970329