MA26754A1 - Composes morpholiniques antagonistes du recepteur de la nk-1. - Google Patents

Composes morpholiniques antagonistes du recepteur de la nk-1.

Info

Publication number
MA26754A1
MA26754A1 MA26111A MA26111A MA26754A1 MA 26754 A1 MA26754 A1 MA 26754A1 MA 26111 A MA26111 A MA 26111A MA 26111 A MA26111 A MA 26111A MA 26754 A1 MA26754 A1 MA 26754A1
Authority
MA
Morocco
Prior art keywords
morpholinic
compounds
receptor antagonist
receptor
compound
Prior art date
Application number
MA26111A
Other languages
English (en)
Inventor
Theresa Maria Ballard
Guy Andrew Higgins
Torsten Hoffmann
Sonia Maria Poli
Andrew Sleight
Original Assignee
Hoffmann La Roche
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 Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of MA26754A1 publication Critical patent/MA26754A1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
    • C07D213/72—Nitrogen atoms
    • C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/06—Anti-spasmodics, e.g. drugs for colics, esophagic dyskinesia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/08—Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/06—Antiasthmatics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • 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
    • 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
    • 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
    • A61P25/22—Anxiolytics
    • 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
    • A61P25/24—Antidepressants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Psychiatry (AREA)
  • Pulmonology (AREA)
  • Rheumatology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Immunology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Hospice & Palliative Care (AREA)
  • Otolaryngology (AREA)
  • Pain & Pain Management (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Abstract

COMPOSÉS MORPHOLINIQUES ANTAGONISTES DU RÉCEPTEUR DE LA NK-1 F. Hoffmann-La Roche AG L'invention a trait à un composé de formule : qui est le 2-(3,5-bis-trifluorométhylphényl)-N-méthyl-N-(6-morpholin-4-yl-4-o-tolylpyridin-3-yl)-isobutyramide. On a trouvé que le composé a une affinité pour le récepteur de la NK-1 et en outre, il est utile dans le traitement de maladies ayant un rapport avec ce récepteur.
MA26111A 1999-11-29 2000-11-28 Composes morpholiniques antagonistes du recepteur de la nk-1. MA26754A1 (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP99123685 1999-11-29

Publications (1)

Publication Number Publication Date
MA26754A1 true MA26754A1 (fr) 2004-12-20

Family

ID=8239481

Family Applications (1)

Application Number Title Priority Date Filing Date
MA26111A MA26754A1 (fr) 1999-11-29 2000-11-28 Composes morpholiniques antagonistes du recepteur de la nk-1.

Country Status (49)

Country Link
EP (1) EP1103545B1 (fr)
JP (1) JP3480835B2 (fr)
KR (1) KR100390117B1 (fr)
CN (1) CN1152016C (fr)
AR (1) AR033659A1 (fr)
AT (1) ATE253561T1 (fr)
AU (1) AU775292B2 (fr)
BG (1) BG64622B1 (fr)
BR (1) BRPI0005616B8 (fr)
CA (1) CA2326529C (fr)
CO (1) CO5251405A1 (fr)
CZ (1) CZ299286B6 (fr)
DE (2) DE60006340T2 (fr)
DK (1) DK1103545T3 (fr)
DO (1) DOP2000000106A (fr)
EA (1) EA004404B1 (fr)
ES (2) ES2208205T3 (fr)
FR (1) FR2801590A1 (fr)
GB (1) GB2356863A (fr)
GC (1) GC0000151A (fr)
GE (1) GEP20022763B (fr)
GT (1) GT200000197A (fr)
HR (1) HRP20000809A2 (fr)
HU (1) HU224703B1 (fr)
ID (1) ID28483A (fr)
IL (1) IL139868A (fr)
IS (1) IS2212B (fr)
IT (1) IT1320120B1 (fr)
JO (1) JO2298B1 (fr)
MA (1) MA26754A1 (fr)
MX (1) MXPA00011672A (fr)
MY (1) MY127426A (fr)
NO (1) NO317264B1 (fr)
NZ (1) NZ508386A (fr)
OA (1) OA11513A (fr)
PA (1) PA8507201A1 (fr)
PE (1) PE20010901A1 (fr)
PL (1) PL195957B1 (fr)
PT (1) PT1103545E (fr)
SG (1) SG97171A1 (fr)
SI (1) SI1103545T1 (fr)
SK (1) SK285373B6 (fr)
SV (1) SV2002000227A (fr)
TN (1) TNSN00226A1 (fr)
TR (1) TR200302077T4 (fr)
UA (1) UA70326C2 (fr)
UY (1) UY26458A1 (fr)
YU (1) YU73400A (fr)
ZA (1) ZA200006964B (fr)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000050398A2 (fr) 1999-02-24 2000-08-31 F. Hoffmann-La Roche Ag Derives de pyridinyl et de phenyle
DK1394150T3 (da) * 1999-02-24 2011-03-21 Hoffmann La Roche 4-phenylpyridinderivater og deres anvendelse som NK-1-receptorantagonister
CN1178917C (zh) * 2000-07-14 2004-12-08 弗·哈夫曼-拉罗切有限公司 作为nk1受体拮抗剂前药的4-苯基-吡啶衍生物的n-氧化物
TWI287003B (en) * 2000-07-24 2007-09-21 Hoffmann La Roche 4-phenyl-pyridine derivatives
TWI259180B (en) * 2000-08-08 2006-08-01 Hoffmann La Roche 4-Phenyl-pyridine derivatives
US20030083345A1 (en) * 2001-07-10 2003-05-01 Torsten Hoffmann Method of treatment and/or prevention of brain, spinal or nerve injury
IL162733A0 (en) * 2002-01-31 2005-11-20 Hoffmann La Roche Genetic polymorphisms in the preprotachykinin gene
HRP20070471T3 (hr) 2003-07-03 2007-11-30 F. Hoffmann - La Roche Ag Dvojni nk1/nk3 antagonisti za liječenje shizofrenije
US7288658B2 (en) 2003-07-15 2007-10-30 Hoffmann-La Roche Inc. Process for preparation of pyridine derivatives
MX2007000198A (es) 2004-07-06 2007-03-15 Hoffmann La Roche Proceso para la preparacion de derivados de carboxamida-piridina utilizados como intermediarios en la sintesis de antagonistas del receptor nk-1.
NZ560232A (en) 2005-02-25 2010-11-26 Hoffmann La Roche Tablets with improved drug substance dispersibility
DK1863767T3 (da) 2005-03-23 2009-05-04 Hoffmann La Roche Metabolitter til NK-I-antagonister til emesis
SI1928427T1 (sl) 2005-09-23 2010-03-31 Hoffmann La Roche Nove formulacije za doziranje
JP2010516731A (ja) 2007-01-24 2010-05-20 グラクソ グループ リミテッド ２−メトキシ−５−（５−トリフルオロメチル−テトラゾール−１−イル）−ベンジル］−（２ｓ−フェニル−ピペリジン−３ｓ−イル）−アミンを含む医薬組成物
US8426450B1 (en) * 2011-11-29 2013-04-23 Helsinn Healthcare Sa Substituted 4-phenyl pyridines having anti-emetic effect
BR112015021982B1 (pt) 2013-03-15 2022-12-13 Global Blood Therapeutics, Inc Compostos e seus usos para a modulação de hemoglobina
BR112016009811A2 (pt) 2013-11-08 2017-12-05 Kissei Pharmaceutical derivado de carboximetil piperidina
SI3102208T2 (sl) 2014-02-07 2024-10-30 Global Blood Therapeutics, Inc. Kristalinični polimorf proste baze 2-hidroksi-6-((2-(1-izopropil-1H-pirazol-5-IL)piridin-3-IL)metoksi)- benzaldehida
TWI649307B (zh) 2014-05-07 2019-02-01 日商橘生藥品工業股份有限公司 Cyclohexylpyridine derivative
KR101948238B1 (ko) 2016-08-19 2019-02-14 (주)케어젠 미녹시딜과 펩타이드의 결합체
KR102328682B1 (ko) 2018-08-27 2021-11-18 주식회사 대웅제약 신규한 헤테로사이클릭아민 유도체 및 이를 포함하는 약학 조성물

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1082959A1 (fr) * 1991-09-20 2001-03-14 Glaxo Group Limited Utilisation des NK1-antagonistes pour le traitement de la depression
IL106142A (en) * 1992-06-29 1997-03-18 Merck & Co Inc Morpholine and thiomorpholine tachykinin receptor antagonists, their preparation and pharmaceutical compositions containing them
IL111960A (en) * 1993-12-17 1999-12-22 Merck & Co Inc Morpholines and thiomorpholines their preparation and pharmaceutical compositions containing them
DE69434063D1 (de) * 1993-12-29 2004-11-11 Merck Sharp & Dohme Substituierte Morpholinderivate und ihre Verwendung als therapeutische Mittel
IL112778A0 (en) * 1994-03-04 1995-05-26 Merck & Co Inc Substituted heterocycles, their preparation and pharmaceutical compositions containing them
TW394773B (en) * 1995-03-24 2000-06-21 Takeda Chemical Industries Ltd Cyclic compounds for antagonizing tachykinin receptor, substance p receptor and neurokinin a receptor, their production and pharmaceutical composition
US5972938A (en) * 1997-12-01 1999-10-26 Merck & Co., Inc. Method for treating or preventing psychoimmunological disorders
DK1394150T3 (da) * 1999-02-24 2011-03-21 Hoffmann La Roche 4-phenylpyridinderivater og deres anvendelse som NK-1-receptorantagonister
US6303790B1 (en) * 1999-11-29 2001-10-16 Hoffman-La Roche Inc. Process for the preparation of pyridine derivatives
CN1178917C (zh) * 2000-07-14 2004-12-08 弗·哈夫曼-拉罗切有限公司 作为nk1受体拮抗剂前药的4-苯基-吡啶衍生物的n-氧化物
TWI287003B (en) * 2000-07-24 2007-09-21 Hoffmann La Roche 4-phenyl-pyridine derivatives
TWI259180B (en) * 2000-08-08 2006-08-01 Hoffmann La Roche 4-Phenyl-pyridine derivatives

Also Published As

Publication number Publication date
SV2002000227A (es) 2002-02-05
YU73400A (sh) 2003-02-28
SK285373B6 (sk) 2006-12-07
PL195957B1 (pl) 2007-11-30
AU775292B2 (en) 2004-07-29
ES2171134A1 (es) 2002-08-16
BRPI0005616B8 (pt) 2021-07-06
EA004404B1 (ru) 2004-04-29
NO20006012D0 (no) 2000-11-28
EA200001114A3 (ru) 2001-12-24
SK17932000A3 (sk) 2001-11-06
FR2801590A1 (fr) 2001-06-01
CA2326529A1 (fr) 2001-05-29
EP1103545B1 (fr) 2003-11-05
CZ299286B6 (cs) 2008-06-04
TR200302077T4 (tr) 2004-01-21
SI1103545T1 (en) 2004-02-29
CZ20004399A3 (cs) 2001-07-11
KR20010051983A (ko) 2001-06-25
CN1152016C (zh) 2004-06-02
GT200000197A (es) 2002-05-22
PA8507201A1 (es) 2002-02-21
HU224703B1 (en) 2006-01-30
UY26458A1 (es) 2001-05-31
SG97171A1 (en) 2003-07-18
BG64622B1 (bg) 2005-09-30
GB2356863A (en) 2001-06-06
ZA200006964B (en) 2001-06-05
EA200001114A2 (ru) 2001-08-27
AU7178700A (en) 2001-05-31
NO20006012L (no) 2001-05-30
JO2298B1 (en) 2005-09-12
NZ508386A (en) 2003-02-28
IT1320120B1 (it) 2003-11-18
ITMI20002575A1 (it) 2002-05-29
DE60006340T2 (de) 2004-09-09
UA70326C2 (en) 2004-10-15
CA2326529C (fr) 2009-12-22
JP2001151754A (ja) 2001-06-05
DE60006340D1 (de) 2003-12-11
HK1036759A1 (en) 2002-01-18
DE10058310A1 (de) 2001-05-31
PE20010901A1 (es) 2001-09-20
DOP2000000106A (es) 2002-07-30
KR100390117B1 (ko) 2003-07-04
BR0005616A (pt) 2001-07-17
CN1297888A (zh) 2001-06-06
GEP20022763B (en) 2002-08-26
EP1103545A1 (fr) 2001-05-30
BG104992A (en) 2001-11-30
AR033659A1 (es) 2004-01-07
GB0028566D0 (en) 2001-01-10
HU0004725D0 (fr) 2001-02-28
ATE253561T1 (de) 2003-11-15
DK1103545T3 (da) 2004-03-15
IL139868A (en) 2009-09-01
MXPA00011672A (es) 2002-08-20
NO317264B1 (no) 2004-09-27
BRPI0005616B1 (pt) 2017-12-12
HRP20000809A2 (en) 2001-12-31
IS2212B (is) 2007-02-15
ES2208205T3 (es) 2004-06-16
PL344147A1 (en) 2001-06-04
IS5725A (is) 2001-05-29
PT1103545E (pt) 2004-03-31
JP3480835B2 (ja) 2003-12-22
IL139868A0 (en) 2002-02-10
MY127426A (en) 2006-11-30
GC0000151A (en) 2005-06-29
CO5251405A1 (es) 2003-02-28
ID28483A (id) 2001-05-31
OA11513A (fr) 2004-02-03
TNSN00226A1 (fr) 2002-05-30
HUP0004725A2 (hu) 2002-04-29

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