JP2005525390A5 - - Google Patents

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Publication number
JP2005525390A5
JP2005525390A5 JP2003579828A JP2003579828A JP2005525390A5 JP 2005525390 A5 JP2005525390 A5 JP 2005525390A5 JP 2003579828 A JP2003579828 A JP 2003579828A JP 2003579828 A JP2003579828 A JP 2003579828A JP 2005525390 A5 JP2005525390 A5 JP 2005525390A5
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JP
Japan
Prior art keywords
formula
compound
salt
amino group
protected amino
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.)
Granted
Application number
JP2003579828A
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English (en)
Japanese (ja)
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JP4490110B2 (ja
JP2005525390A (ja
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Publication date
Priority claimed from GBGB0207449.0A external-priority patent/GB0207449D0/en
Application filed filed Critical
Publication of JP2005525390A publication Critical patent/JP2005525390A/ja
Publication of JP2005525390A5 publication Critical patent/JP2005525390A5/ja
Application granted granted Critical
Publication of JP4490110B2 publication Critical patent/JP4490110B2/ja
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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JP2003579828A 2002-03-28 2003-03-27 炎症性症状の治療のためのccr3拮抗薬としての、n−{[(2s)−4−(3,4−ジフルオロベンジル)モルホリン−2−イル]メチル}−2−{3−[(メチルスルホニル)アミノ]フェニル}アセトアミド Expired - Lifetime JP4490110B2 (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB0207449.0A GB0207449D0 (en) 2002-03-28 2002-03-28 Novel compounds
PCT/EP2003/003339 WO2003082291A1 (en) 2002-03-28 2003-03-27 N-{´ (2s) -4- (3, 4-difluorobenzyl) morpholin-2yl!methyl} -2-{3-' (methylsulphonyl) amino! phenyl}acetamide as ccr3 antagonist for the treatment of inflammatory conditions

Publications (3)

Publication Number Publication Date
JP2005525390A JP2005525390A (ja) 2005-08-25
JP2005525390A5 true JP2005525390A5 (https=) 2006-05-18
JP4490110B2 JP4490110B2 (ja) 2010-06-23

Family

ID=9933998

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2003579828A Expired - Lifetime JP4490110B2 (ja) 2002-03-28 2003-03-27 炎症性症状の治療のためのccr3拮抗薬としての、n−{[(2s)−4−(3,4−ジフルオロベンジル)モルホリン−2−イル]メチル}−2−{3−[(メチルスルホニル)アミノ]フェニル}アセトアミド

Country Status (22)

Country Link
US (1) US20060058299A1 (https=)
EP (1) EP1487453B1 (https=)
JP (1) JP4490110B2 (https=)
KR (1) KR20040095347A (https=)
CN (1) CN1642553A (https=)
AR (1) AR039177A1 (https=)
AT (1) ATE454892T1 (https=)
AU (1) AU2003216905A1 (https=)
BR (1) BR0308719A (https=)
CA (1) CA2479910A1 (https=)
DE (1) DE60330952D1 (https=)
ES (1) ES2339436T3 (https=)
GB (1) GB0207449D0 (https=)
IL (1) IL163648A0 (https=)
IS (1) IS7415A (https=)
MX (1) MXPA04009458A (https=)
NO (1) NO20044098L (https=)
PL (1) PL372930A1 (https=)
RU (1) RU2004126145A (https=)
TW (1) TW200400823A (https=)
WO (1) WO2003082291A1 (https=)
ZA (1) ZA200406990B (https=)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004028530A1 (en) 2002-09-26 2004-04-08 Bristol-Myers Squibb Company N-substituted heterocyclic amines as modulators of chemokine receptor activity
WO2007011292A1 (en) * 2005-07-21 2007-01-25 Astrazeneca Ab N-benzyl-morpholine derivatives as modulators of the chemokine receptor
HUP0500886A2 (en) * 2005-09-23 2007-05-29 Sanofi Aventis Amide derivatives as ccr3 receptor ligands, process for producing them, pharmaceutical compositions containing them and their use
HUP0500877A2 (en) * 2005-09-22 2007-05-29 Sanofi Aventis Amide derivatives as ccr3 receptor ligands, process for producing them, pharmaceutical compositions containing them and their use and intermediates
BRPI0616150A2 (pt) * 2005-09-22 2011-06-07 Sanofi Aventis derivados de amino-alquil-amida como lìquidos receptores de ccr3
HUP0800478A2 (en) * 2008-07-31 2010-03-01 Sanofi Aventis Substituted pyrrolidinyl-[1,3]thiazolo[4,5-b]pyridin derivatives as ccr3 receptor ligands
EP2785338A1 (en) * 2011-12-01 2014-10-08 Glaxo Group Limited Methods of treatment and prevention of eye diseases

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS562929A (en) * 1979-06-21 1981-01-13 Sumitomo Chem Co Ltd Preparation of optically active cyclopentenolone
CZ284687B6 (cs) * 1986-04-30 1999-02-17 Dainippon Pharmaceutical Co., Ltd. Substituovaný benzamidový derivát, způsob jeho výroby a farmaceutický prostředek na jeho bázi
JPH01117882A (ja) * 1987-10-30 1989-05-10 Dainippon Pharmaceut Co Ltd 複素環式カルボン酸アミド誘導体
JPH03291274A (ja) * 1990-04-09 1991-12-20 Yoshitomi Pharmaceut Ind Ltd アミノアルキルモルホリン誘導体の製造法
JPH04270272A (ja) * 1991-02-25 1992-09-25 Yoshitomi Pharmaceut Ind Ltd アミノアルキルモルホリン誘導体の製造法
TW223629B (https=) * 1992-03-06 1994-05-11 Hoffmann La Roche
US5219856A (en) * 1992-04-06 1993-06-15 E. I. Du Pont De Nemours And Company Angiotensin-II receptor blocking, heterocycle substituted imidazoles
US6031097A (en) * 1997-10-27 2000-02-29 Neurogen Corporation 1-(N-(arylalkylaminoalkyl) aminoisoquinolines; a new class of dopamine receptor subtype specific ligands
US6331545B1 (en) * 1998-12-18 2001-12-18 Soo S. Ko Heterocycyclic piperidines as modulators of chemokine receptor activity
HUP0202712A3 (en) * 1999-09-14 2004-12-28 Aventis Pharmaceuticals Inc Br Thienoisoxazole phenoxy unsubstituted ethyl and propyl derivatives useful as d4 antagonists, their intermediates, process for their preparation and pharmaceutical compositions containing the compounds
EP1324990B1 (en) * 2000-09-29 2014-10-29 Glaxo Group Limited Morpholin-acetamide derivatives for the treatment of inflammatory diseases
BR0114321A (pt) * 2000-09-29 2003-07-01 Glaxo Group Ltd Composto, composição farmacêutica, uso de um composto, método de tratamento ou profilaxia de doenças inflamatórias, e, processo para preparar um composto

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