JP2004504400A5 - - Google Patents

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Publication number
JP2004504400A5
JP2004504400A5 JP2002514138A JP2002514138A JP2004504400A5 JP 2004504400 A5 JP2004504400 A5 JP 2004504400A5 JP 2002514138 A JP2002514138 A JP 2002514138A JP 2002514138 A JP2002514138 A JP 2002514138A JP 2004504400 A5 JP2004504400 A5 JP 2004504400A5
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JP
Japan
Prior art keywords
methyl
compound
formula
bis
trifluoromethyl
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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.)
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Application number
JP2002514138A
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English (en)
Japanese (ja)
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JP4118673B2 (ja
JP2004504400A (ja
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Publication date
Application filed filed Critical
Priority claimed from PCT/EP2001/008432 external-priority patent/WO2002008232A1/en
Publication of JP2004504400A publication Critical patent/JP2004504400A/ja
Publication of JP2004504400A5 publication Critical patent/JP2004504400A5/ja
Application granted granted Critical
Publication of JP4118673B2 publication Critical patent/JP4118673B2/ja
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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JP2002514138A 2000-07-24 2001-07-20 ニューロキニン1受容体アンタゴニストとしての4−フェニル−ピリジン誘導体 Expired - Lifetime JP4118673B2 (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP00115846 2000-07-24
PCT/EP2001/008432 WO2002008232A1 (en) 2000-07-24 2001-07-20 4-phenyl-pyridine derivatives as neurokinin-1 receptor antagonists

Publications (3)

Publication Number Publication Date
JP2004504400A JP2004504400A (ja) 2004-02-12
JP2004504400A5 true JP2004504400A5 (cg-RX-API-DMAC7.html) 2005-02-24
JP4118673B2 JP4118673B2 (ja) 2008-07-16

Family

ID=8169331

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2002514138A Expired - Lifetime JP4118673B2 (ja) 2000-07-24 2001-07-20 ニューロキニン1受容体アンタゴニストとしての4−フェニル−ピリジン誘導体

Country Status (37)

Country Link
US (2) US6576762B2 (cg-RX-API-DMAC7.html)
EP (1) EP1305319B1 (cg-RX-API-DMAC7.html)
JP (1) JP4118673B2 (cg-RX-API-DMAC7.html)
KR (1) KR100527214B1 (cg-RX-API-DMAC7.html)
CN (1) CN1192032C (cg-RX-API-DMAC7.html)
AR (1) AR029875A1 (cg-RX-API-DMAC7.html)
AT (1) ATE322496T1 (cg-RX-API-DMAC7.html)
AU (2) AU8200501A (cg-RX-API-DMAC7.html)
BR (1) BR0112695A (cg-RX-API-DMAC7.html)
CA (1) CA2416874C (cg-RX-API-DMAC7.html)
CY (1) CY1106113T1 (cg-RX-API-DMAC7.html)
CZ (1) CZ2003528A3 (cg-RX-API-DMAC7.html)
DE (1) DE60118569T2 (cg-RX-API-DMAC7.html)
DK (1) DK1305319T3 (cg-RX-API-DMAC7.html)
EC (1) ECSP034446A (cg-RX-API-DMAC7.html)
ES (1) ES2260265T3 (cg-RX-API-DMAC7.html)
GT (1) GT200100148A (cg-RX-API-DMAC7.html)
HR (1) HRP20030031A2 (cg-RX-API-DMAC7.html)
HU (1) HU229231B1 (cg-RX-API-DMAC7.html)
IL (2) IL153837A0 (cg-RX-API-DMAC7.html)
JO (1) JO2321B1 (cg-RX-API-DMAC7.html)
MA (1) MA26933A1 (cg-RX-API-DMAC7.html)
MX (1) MXPA03000367A (cg-RX-API-DMAC7.html)
MY (1) MY129224A (cg-RX-API-DMAC7.html)
NO (1) NO20030353D0 (cg-RX-API-DMAC7.html)
NZ (1) NZ523452A (cg-RX-API-DMAC7.html)
PA (1) PA8522801A1 (cg-RX-API-DMAC7.html)
PE (1) PE20020258A1 (cg-RX-API-DMAC7.html)
PL (1) PL366173A1 (cg-RX-API-DMAC7.html)
PT (1) PT1305319E (cg-RX-API-DMAC7.html)
RU (1) RU2276139C2 (cg-RX-API-DMAC7.html)
SI (1) SI1305319T1 (cg-RX-API-DMAC7.html)
TW (1) TWI287003B (cg-RX-API-DMAC7.html)
UY (1) UY26851A1 (cg-RX-API-DMAC7.html)
WO (1) WO2002008232A1 (cg-RX-API-DMAC7.html)
YU (1) YU2803A (cg-RX-API-DMAC7.html)
ZA (1) ZA200300219B (cg-RX-API-DMAC7.html)

Families Citing this family (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1103545B1 (en) * 1999-11-29 2003-11-05 F. Hoffmann-La Roche Ag 2-(3,5-Bis-trifluoromethyl-phenyl)-N-methyl-N-(6-morpholin-4-yl-4-o-tolyl-pyridin-3-yl)-isobutyramide
MXPA04010622A (es) 2002-04-26 2005-01-25 Lilly Co Eli Derivados de triazol como antagonistas de receptor de taquicinina.
WO2003091227A1 (en) 2002-04-26 2003-11-06 Eli Lilly And Company Tachykinin receptor antagonists
AU2003300018A1 (en) * 2002-10-11 2004-05-04 Bristol-Myers Squibb Company Process for the preparation of tri-nitrogen containing heteroaryl-diamine derivatives useful as pharmaceutical agents and methods of producing pharmaceutical agents
EP1638944A1 (en) * 2003-06-12 2006-03-29 Eli Lilly And Company Tachykinin receptor antagonists
KR100744859B1 (ko) * 2003-07-03 2007-08-01 에프. 호프만-라 로슈 아게 정신분열증 치료를 위한 이중 nk1/nk3 길항물질
US7288658B2 (en) * 2003-07-15 2007-10-30 Hoffmann-La Roche Inc. Process for preparation of pyridine derivatives
CN1984891B (zh) 2004-07-06 2012-08-08 弗·哈夫曼-拉罗切有限公司 用作合成nk-1受体拮抗剂的中间体的甲酰胺吡啶衍生物的制备方法
US20060030600A1 (en) * 2004-08-06 2006-02-09 Patrick Schnider Dual NK1/NK3 receptor antagonists for the treatment of schizophrenia
AU2005286733B2 (en) * 2004-09-23 2009-11-05 Alexander Michalow Methods for regulating neurotransmitter systems by inducing counteradaptations
US20080045610A1 (en) * 2004-09-23 2008-02-21 Alexander Michalow Methods for regulating neurotransmitter systems by inducing counteradaptations
EP1855655A2 (en) 2005-02-25 2007-11-21 F. Hoffmann-Roche AG Tablets with improved drug substance dispersibility
US8067662B2 (en) 2009-04-01 2011-11-29 Aalnex, Inc. Systems and methods for wound protection and exudate management
US7816577B2 (en) 2006-02-13 2010-10-19 Aalnex, Inc. Wound shield
WO2007137954A1 (en) 2006-05-31 2007-12-06 F. Hoffmann-La Roche Ag Aryl-4-ethynyl-isoxazole derivatives
CN101641099A (zh) 2007-01-24 2010-02-03 葛兰素集团有限公司 包含3,5-二氨基-6-(2,3-二氯苯基)-1,2,4-三嗪或r(-)-2,4-二氨基-5-(2,3-二氯苯基)-6-氟甲基嘧啶和nk1的药物组合物
GB0808747D0 (en) 2008-05-14 2008-06-18 Glaxo Wellcome Mfg Pte Ltd Novel compounds
US8426450B1 (en) * 2011-11-29 2013-04-23 Helsinn Healthcare Sa Substituted 4-phenyl pyridines having anti-emetic effect
BR112016009811A2 (pt) 2013-11-08 2017-12-05 Kissei Pharmaceutical derivado de carboximetil piperidina
TWI649307B (zh) 2014-05-07 2019-02-01 日商橘生藥品工業股份有限公司 Cyclohexylpyridine derivative
US10538491B2 (en) 2015-03-16 2020-01-21 Vanderbilt University 4,5-substituted picolinamide and picolinonitrile metabotropic glutamate receptor 2 negative allosteric modulators
CN108712913B (zh) * 2015-12-22 2022-06-24 武田药品工业株式会社 内体g蛋白-偶联的受体的三部分调节剂
US20210015834A1 (en) 2018-02-26 2021-01-21 Ospedale San Raffaele S.R.L. Nk-1 antagonists for use in the treatment of ocular pain

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IL111960A (en) 1993-12-17 1999-12-22 Merck & Co Inc Morpholines and thiomorpholines their preparation and pharmaceutical compositions containing them
WO1995018124A1 (en) 1993-12-29 1995-07-06 Merck Sharp & Dohme Limited Substituted morpholine derivatives and their use as therapeutic agents
IL112778A0 (en) 1994-03-04 1995-05-26 Merck & Co Inc Substituted heterocycles, their preparation and pharmaceutical compositions containing them
US5972938A (en) 1997-12-01 1999-10-26 Merck & Co., Inc. Method for treating or preventing psychoimmunological disorders
JPH11322748A (ja) * 1998-03-19 1999-11-24 Takeda Chem Ind Ltd 複素環化合物、その製造法および用途
EP1061926A2 (en) 1998-03-19 2000-12-27 Takeda Chemical Industries, Ltd. Heterocyclic compounds, their production and use as tachykinin receptor antagonists
SI1035115T1 (en) * 1999-02-24 2005-02-28 F. Hoffmann-La Roche Ag 4-Phenylpyridine derivatives and their use as NK-1 receptor antagonists
HRP20010604A2 (en) * 1999-02-24 2002-08-31 Hoffmann La Roche 3-phenylpyridine derivatives and their use as nk-1 receptor antagonists
CN1131212C (zh) * 1999-02-24 2003-12-17 弗·哈夫曼-拉罗切有限公司 苯基-和吡啶基衍生物
US6291465B1 (en) * 1999-03-09 2001-09-18 Hoffmann-La Roche Inc. Biphenyl derivatives
US6303790B1 (en) * 1999-11-29 2001-10-16 Hoffman-La Roche Inc. Process for the preparation of pyridine derivatives
EP1103545B1 (en) * 1999-11-29 2003-11-05 F. Hoffmann-La Roche Ag 2-(3,5-Bis-trifluoromethyl-phenyl)-N-methyl-N-(6-morpholin-4-yl-4-o-tolyl-pyridin-3-yl)-isobutyramide
CZ303639B6 (cs) * 2000-07-14 2013-01-23 F. Hoffmann-La Roche Ag N-Oxid derivátu 4-fenylpyridinu, zpusob jeho prípravy a lécivo s jeho obsahem

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