[go: up one dir, main page]

WO2003082819A1 - Derive de n-phenyl-n-(4-piperidinyl)amide - Google Patents

Derive de n-phenyl-n-(4-piperidinyl)amide Download PDF

Info

Publication number
WO2003082819A1
WO2003082819A1 PCT/JP2003/003948 JP0303948W WO03082819A1 WO 2003082819 A1 WO2003082819 A1 WO 2003082819A1 JP 0303948 W JP0303948 W JP 0303948W WO 03082819 A1 WO03082819 A1 WO 03082819A1
Authority
WO
WIPO (PCT)
Prior art keywords
phenyl
piperidinyl
amide derivative
derivative
salt
Prior art date
Legal status (The legal status 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 status listed.)
Ceased
Application number
PCT/JP2003/003948
Other languages
English (en)
Japanese (ja)
Inventor
Toshihiro Takahashi
Kunio Kobayashi
Shinichi Yoshida
Tsuyoshi Endo
Nobutaka Mochiduki
Tomio Yamakawa
Kiichi Shika
Toru Kawasaki
Kenji Hirate
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nippon Chemiphar Co Ltd
Original Assignee
Nippon Chemiphar Co Ltd
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 Nippon Chemiphar Co Ltd filed Critical Nippon Chemiphar Co Ltd
Priority to JP2003580287A priority Critical patent/JPWO2003082819A1/ja
Priority to AU2003220898A priority patent/AU2003220898A1/en
Publication of WO2003082819A1 publication Critical patent/WO2003082819A1/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D211/60Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D211/62Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals attached in position 4
    • C07D211/66Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals attached in position 4 having a hetero atom as the second substituent in position 4
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/02Drugs for disorders of the nervous system for peripheral neuropathies
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D211/56Nitrogen atoms
    • C07D211/58Nitrogen atoms attached in position 4

Landscapes

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

Abstract

La présente invention a trait à un dérivé de N-phényl-N-(4-pipéridinyl)amide représenté par la formule générale (I), dans laquelle : R1 représente alkyle en C1-C6 ; R2 et R4 représentent chacun phényle éventuellement substitué ; R3 représente hydrogène, alcoxycarbonyle en C2-C8, ou méthyle substitué par alcoxy en C1-C6 ; R5 représente un résidu d'acide aminé tel que glycine, alanine, leucine, ou phénylalanine ; et m et n représente 1 ou 2 ; ou un sel du dérivé. L'invention a trait également à un analgésique contenant le dérivé ou sel en tant que principe actif.
PCT/JP2003/003948 2002-04-01 2003-03-28 Derive de n-phenyl-n-(4-piperidinyl)amide Ceased WO2003082819A1 (fr)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP2003580287A JPWO2003082819A1 (ja) 2002-04-01 2003-03-28 N−フェニル−n−(4−ピペリジニル)アミド誘導体
AU2003220898A AU2003220898A1 (en) 2002-04-01 2003-03-28 N-phenyl-n-(4-piperidinyl)amide derivative

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2002-098443 2002-04-01
JP2002098443 2002-04-01

Publications (1)

Publication Number Publication Date
WO2003082819A1 true WO2003082819A1 (fr) 2003-10-09

Family

ID=28671952

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2003/003948 Ceased WO2003082819A1 (fr) 2002-04-01 2003-03-28 Derive de n-phenyl-n-(4-piperidinyl)amide

Country Status (3)

Country Link
JP (1) JPWO2003082819A1 (fr)
AU (1) AU2003220898A1 (fr)
WO (1) WO2003082819A1 (fr)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004046107A1 (fr) * 2002-11-19 2004-06-03 Takeda Pharmaceutical Company Limited Derives d'indole servant d'antagoniste de somatostatine
WO2005030722A1 (fr) * 2003-09-29 2005-04-07 Nippon Chemiphar Co., Ltd. Derive d'amide de n-(4-piperidinyle) n-substitue
WO2006030931A1 (fr) * 2004-09-14 2006-03-23 Nippon Chemiphar Co., Ltd. Derive d’amide n-(4-piperidinyl) n-substitue
JP2008511576A (ja) * 2004-08-31 2008-04-17 チバ スペシャルティ ケミカルズ ホールディング インコーポレーテッド 有機材料の安定化
US10766925B2 (en) * 2016-04-11 2020-09-08 Arizona Board Of Regents On Behalf Of The University Of Arizona Opioid receptor modulators

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1995028931A1 (fr) * 1994-04-26 1995-11-02 Merck & Co., Inc. Azacycles spiro-substitues utilises en tant qu'antagonistes de neurokinine-3
JPH08337569A (ja) * 1995-06-15 1996-12-24 Sankyo Co Ltd 鎮痛活性物質
WO1999045011A1 (fr) * 1998-03-06 1999-09-10 Janssen Pharmaceutica N.V. Inhibiteurs du transport de la glycine

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1995028931A1 (fr) * 1994-04-26 1995-11-02 Merck & Co., Inc. Azacycles spiro-substitues utilises en tant qu'antagonistes de neurokinine-3
JPH08337569A (ja) * 1995-06-15 1996-12-24 Sankyo Co Ltd 鎮痛活性物質
WO1999045011A1 (fr) * 1998-03-06 1999-09-10 Janssen Pharmaceutica N.V. Inhibiteurs du transport de la glycine

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004046107A1 (fr) * 2002-11-19 2004-06-03 Takeda Pharmaceutical Company Limited Derives d'indole servant d'antagoniste de somatostatine
WO2005030722A1 (fr) * 2003-09-29 2005-04-07 Nippon Chemiphar Co., Ltd. Derive d'amide de n-(4-piperidinyle) n-substitue
JP2008511576A (ja) * 2004-08-31 2008-04-17 チバ スペシャルティ ケミカルズ ホールディング インコーポレーテッド 有機材料の安定化
US9051448B2 (en) 2004-08-31 2015-06-09 Basf Se Stabilization of organic materials
WO2006030931A1 (fr) * 2004-09-14 2006-03-23 Nippon Chemiphar Co., Ltd. Derive d’amide n-(4-piperidinyl) n-substitue
US10766925B2 (en) * 2016-04-11 2020-09-08 Arizona Board Of Regents On Behalf Of The University Of Arizona Opioid receptor modulators

Also Published As

Publication number Publication date
AU2003220898A1 (en) 2003-10-13
JPWO2003082819A1 (ja) 2005-08-04

Similar Documents

Publication Publication Date Title
WO2003076458A3 (fr) Inhibiteurs
EP1674452A4 (fr) Nouveau derive de 4-phenylamino-benzaldoxime et son utilisation en tant qu'inhibiteur de mek
IL147651A0 (en) Isoxazoline derivative and herbicide containing the same as the active ingredient
AU2003246100A1 (en) Amide derivative
CA2424600A1 (fr) Composes aliphatiques azotes a noyau a cinq elements
AU2003275826A1 (en) Macrocyclic peptides active against the hepatitis c virus
MY127791A (en) Hepatitis c inhibitor tri-peptides
TW200602322A (en) Phosphodiesterase 4 inhibitors, including n-substituted diarylamine analogs
FI950309A0 (fi) Proliiniamidijohdannaisia
WO2003064455A3 (fr) Peptides macrocycliques actifs contre le virus de l'hepatite c
NZ536734A (en) Spiroindolinepiperidine derivatives
WO2007056517A3 (fr) Nouveaux sels pharmaceutiques et polymorphes d'un inhibiteur du facteur xa
ATE374765T1 (de) Substituierte heterocyclische amide
DK1008592T3 (da) Cykliske amidderivater, som inhiberer cathepsin K
MXPA06003253A (es) Derivados de acido acetico substituidos.
DK0615978T3 (da) Peptidderivater af borsyre med proteaseinhiberende virkning, fremgangsmåde til fremstilling heraf samt farmaceutiske sammen
WO2003064429A1 (fr) Thienopyrimidines, procedes de fabrication et d'utilisation correspondants
EP1295876A4 (fr) Amides d'acide carboxylique, azides et amino-alcools et procedes de preparation de alpha-ceto amides a l'aide de ces derniers
EA200400994A1 (ru) Новые 1,2,3-замещенные производные индолизина, являющиеся ингибиторами факторов роста фибробластов, способ их получения и фармацевтические композиции, содержащие их
MXPA05013584A (es) Compuesto amina terciaria ciclica.
EP1553096A4 (fr) Composes pyrazole
WO2003082819A1 (fr) Derive de n-phenyl-n-(4-piperidinyl)amide
AU2003241060A1 (en) New atorvastatin salts and pharmaceutical compositions containing them
AR044175A1 (es) Compuestos de cefemo
ATE373636T1 (de) Amidderivate als inhibitoren der enzymatischen aktivität von renin

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NI NO NZ OM PH PL PT RO RU SC SD SE SG SK SL TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): GH GM KE LS MW MZ SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IT LU MC NL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
WWE Wipo information: entry into national phase

Ref document number: 2003580287

Country of ref document: JP

122 Ep: pct application non-entry in european phase