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AR002025A1 - Derivados de 4-(1h-indol-1-il)-1-piperidinilo, su uso y un procedimiento para su preparacion, una composicion farmaceutica que los contiene, unprocedimiento para la preparacion de dicha composicion farmaceutica. - Google Patents

Derivados de 4-(1h-indol-1-il)-1-piperidinilo, su uso y un procedimiento para su preparacion, una composicion farmaceutica que los contiene, unprocedimiento para la preparacion de dicha composicion farmaceutica.

Info

Publication number
AR002025A1
AR002025A1 ARP960101210A AR10121096A AR002025A1 AR 002025 A1 AR002025 A1 AR 002025A1 AR P960101210 A ARP960101210 A AR P960101210A AR 10121096 A AR10121096 A AR 10121096A AR 002025 A1 AR002025 A1 AR 002025A1
Authority
AR
Argentina
Prior art keywords
preparation
procedure
pharmaceutical composition
alkyl
indol
Prior art date
Application number
ARP960101210A
Other languages
English (en)
Original Assignee
Janssen Pharmaceutica Nv
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 Janssen Pharmaceutica Nv filed Critical Janssen Pharmaceutica Nv
Publication of AR002025A1 publication Critical patent/AR002025A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/18Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D513/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04Ortho-condensed systems

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)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

La presente invención se refiere a los compuestos que tienen la fórmula (I) a sus sales de adición de ácido farmacéuticamente aceptable y a las formasestereoquímicamente isoméricas de los mismos donde la línea de trazos designa un enlace opcional;R1 y R2 son cada uno independientemente hidrógeno, alquiloC1-6, fenilo o fenilo sustituido con 1, 2 ó 3 sustituyentes seleccionados de halo, hidroxi, nitro, ciano, trifluormetilo, alquilo C1-6, alquiloxi C1-6,alquiltio C1-6, mercapto, amino, monoy di(alquilo C1-6)amino, carboxilo, alcoxicarbonilo C1-6 y alquilcarbinilo C1-6; Alk es alcanodiilo C1-4; D es unapirimidinona, piperidona o bencimidozolidinona; que tiene actividad antipsicótica; su preparación, las composiciones que lo contienen y su uso enmedicina.
ARP960101210A 1995-01-31 1996-01-30 Derivados de 4-(1h-indol-1-il)-1-piperidinilo, su uso y un procedimiento para su preparacion, una composicion farmaceutica que los contiene, unprocedimiento para la preparacion de dicha composicion farmaceutica. AR002025A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP95200229 1995-01-31

Publications (1)

Publication Number Publication Date
AR002025A1 true AR002025A1 (es) 1998-01-07

Family

ID=8219983

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP960101210A AR002025A1 (es) 1995-01-31 1996-01-30 Derivados de 4-(1h-indol-1-il)-1-piperidinilo, su uso y un procedimiento para su preparacion, una composicion farmaceutica que los contiene, unprocedimiento para la preparacion de dicha composicion farmaceutica.

Country Status (21)

Country Link
US (1) US5919788A (es)
EP (1) EP0808313B1 (es)
JP (1) JP3980054B2 (es)
KR (1) KR100415391B1 (es)
CN (1) CN1152874C (es)
AR (1) AR002025A1 (es)
AT (1) ATE247105T1 (es)
AU (1) AU702931B2 (es)
BR (1) BR9606815A (es)
CA (1) CA2210913C (es)
DE (1) DE69629454T2 (es)
ES (1) ES2205015T3 (es)
FI (1) FI973164A0 (es)
IL (1) IL116930A (es)
MY (1) MY130950A (es)
NO (1) NO308537B1 (es)
NZ (1) NZ301264A (es)
PL (1) PL183291B1 (es)
TW (1) TW421649B (es)
WO (1) WO1996023784A1 (es)
ZA (1) ZA96702B (es)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI242011B (en) * 1997-03-31 2005-10-21 Eisai Co Ltd 1,4-substituted cyclic amine derivatives
US7189753B1 (en) 1997-11-06 2007-03-13 Cady Roger K Preemptive prophylaxis of migraine
US6204274B1 (en) 1998-04-29 2001-03-20 American Home Products Corporation Indolyl derivatives as serotonergic agents
TW528754B (en) * 1998-04-29 2003-04-21 Wyeth Corp Indolyl derivatibes as serotonergic agents
GB9810886D0 (en) * 1998-05-13 1998-07-22 Lilly Industries Ltd Pharmaceutical compounds
EP1791839B1 (en) * 2004-09-09 2015-06-10 Janssen Pharmaceutica NV Preparation of 9-hydroxy-3-(2-hydroxyethyl)-2-methyl-4h-pyrido[1,2-a]pyrimidin-4-one and crystalls thereof
JP2009524574A (ja) * 2006-08-23 2009-07-02 テバ ファーマシューティカル インダストリーズ リミティド Cmhtp及びその中間体の合成方法
US7820816B2 (en) 2006-08-23 2010-10-26 Teva Pharmaceutical Industries Ltd. Process for the synthesis of CMHTP and intermediates thereof
CN101600716A (zh) * 2007-01-08 2009-12-09 阿特维斯集团公司 用于制备9-羟基-3-(2-氯乙基)-2-甲基-4H-吡啶并[1,2-a]嘧啶-4-酮盐酸盐的改进方法
WO2008126886A1 (ja) * 2007-04-12 2008-10-23 Taisho Pharmaceutical Co., Ltd. インドール又はインドリン誘導体
WO2009010988A1 (en) * 2007-07-19 2009-01-22 Natco Pharma Limited An improved, industrially viable process for the preparation of high purity paliperidone
WO2012177708A1 (en) 2011-06-20 2012-12-27 Ratiopharm Gmbh Paliperidone oleate
WO2014102588A2 (en) * 2012-12-27 2014-07-03 Purdue Pharma L.P. Indole and indoline-type piperidine compounds and uses thereof
US9951038B2 (en) 2012-12-27 2018-04-24 Purdue Pharma L.P. Quinazolin-4(3H)-one-type piperidine compounds and uses thereof
CN117700410B (zh) * 2023-05-20 2025-07-04 山东康诺生物工程有限公司 一种3-(2-氯乙基)-2-甲基-9-羟基-4H-吡啶并[1,2-a]嘧啶-4-酮的制备方法

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4342870A (en) * 1980-03-28 1982-08-03 Janssen Pharmaceutica N.V. Novel 3-(1-piperidinylalkyl)-4H-pyrido[1,2-a]pyrimidin-4-one derivatives
US4443451A (en) * 1981-07-15 1984-04-17 Janssen Pharmaceutica N.V. Bicyclic pyrimidin-5-one derivatives
US5140029A (en) * 1989-01-09 1992-08-18 Janssen Pharmaceutica N.V. 2-aminopyrimidinone derivatives
US5256659A (en) * 1989-01-09 1993-10-26 Janssen Pharmaceutica N.V. 2-aminopyrimidinone derivatives
GB8900382D0 (en) * 1989-01-09 1989-03-08 Janssen Pharmaceutica Nv 2-aminopyrimidinone derivatives
JP2800953B2 (ja) * 1990-07-06 1998-09-21 住友製薬株式会社 新規なイミド誘導体
US5360807A (en) * 1990-07-19 1994-11-01 Janssen Pharmaceutica N.V. Substituted thiazolyl and substituted pyridinyl derivatives
DK181190D0 (da) * 1990-07-30 1990-07-30 Lundbeck & Co As H 3-aryl-indol- eller 3-aryl-indazolderivater
GB9305641D0 (en) * 1993-03-18 1993-05-05 Merck Sharp & Dohme Therapeutic agents

Also Published As

Publication number Publication date
AU4664596A (en) 1996-08-21
FI973164L (fi) 1997-07-30
ES2205015T3 (es) 2004-05-01
DE69629454D1 (en) 2003-09-18
MX9705821A (es) 1997-10-31
MY130950A (en) 2007-07-31
WO1996023784A1 (en) 1996-08-08
NZ301264A (en) 1998-07-28
KR19980701692A (ko) 1998-06-25
BR9606815A (pt) 1997-12-30
PL321565A1 (en) 1997-12-08
FI973164A7 (fi) 1997-07-30
EP0808313A1 (en) 1997-11-26
DE69629454T2 (de) 2004-06-17
CA2210913A1 (en) 1996-08-08
CN1152874C (zh) 2004-06-09
NO973508L (no) 1997-07-30
ATE247105T1 (de) 2003-08-15
PL183291B1 (pl) 2002-06-28
CN1172482A (zh) 1998-02-04
AU702931B2 (en) 1999-03-11
TW421649B (en) 2001-02-11
KR100415391B1 (ko) 2004-05-06
CA2210913C (en) 2008-10-21
EP0808313B1 (en) 2003-08-13
FI973164A0 (fi) 1997-07-30
JP3980054B2 (ja) 2007-09-19
IL116930A (en) 2000-06-29
NO308537B1 (no) 2000-09-25
JPH10512893A (ja) 1998-12-08
US5919788A (en) 1999-07-06
IL116930A0 (en) 1996-05-14
NO973508D0 (no) 1997-07-30
ZA96702B (en) 1997-07-30

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