ATE454892T1 - N- (2s)-4-(3,4-difluorobenzyl)morpholin-2-yl methyl -2- 3- (methylsulphonyl)amino phenyl acetamid als ccr3 antagonist für die behandlung von entzündlichen erkrankungen - Google Patents

N- (2s)-4-(3,4-difluorobenzyl)morpholin-2-yl methyl -2- 3- (methylsulphonyl)amino phenyl acetamid als ccr3 antagonist für die behandlung von entzündlichen erkrankungen

Info

Publication number
ATE454892T1
ATE454892T1 AT03712117T AT03712117T ATE454892T1 AT E454892 T1 ATE454892 T1 AT E454892T1 AT 03712117 T AT03712117 T AT 03712117T AT 03712117 T AT03712117 T AT 03712117T AT E454892 T1 ATE454892 T1 AT E454892T1
Authority
AT
Austria
Prior art keywords
methylsulphonyl
difluorobenzyl
morpholine
methyl
treatment
Prior art date
Application number
AT03712117T
Other languages
German (de)
English (en)
Inventor
Rachael Ancliff
Caroline Cook
Colin Eldred
Paul Gore
Lee Harrison
Martin Hayes
Simon Hodgson
Duncan Judd
Suzanne KEELING
Xiao Lewell
Gail Mills
Graeme Robertson
Stephen Swanson
Andrew Walker
Mark Wilkinson
Original Assignee
Glaxo Group 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 Glaxo Group Ltd filed Critical Glaxo Group Ltd
Application granted granted Critical
Publication of ATE454892T1 publication Critical patent/ATE454892T1/de

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D265/00Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
    • C07D265/281,4-Oxazines; Hydrogenated 1,4-oxazines
    • C07D265/301,4-Oxazines; Hydrogenated 1,4-oxazines not condensed with other rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/70Carbohydrates; Sugars; Derivatives thereof
    • A61K31/7042Compounds having saccharide radicals and heterocyclic rings
    • A61K31/7052Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
    • A61K31/7056Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing five-membered rings with nitrogen as a ring hetero atom
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/02Nasal agents, e.g. decongestants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • 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]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/08Antiallergic agents

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Pulmonology (AREA)
  • Epidemiology (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Immunology (AREA)
  • Otolaryngology (AREA)
  • Dermatology (AREA)
  • Molecular Biology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
AT03712117T 2002-03-28 2003-03-27 N- (2s)-4-(3,4-difluorobenzyl)morpholin-2-yl methyl -2- 3- (methylsulphonyl)amino phenyl acetamid als ccr3 antagonist für die behandlung von entzündlichen erkrankungen ATE454892T1 (de)

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 (1)

Publication Number Publication Date
ATE454892T1 true ATE454892T1 (de) 2010-01-15

Family

ID=9933998

Family Applications (1)

Application Number Title Priority Date Filing Date
AT03712117T ATE454892T1 (de) 2002-03-28 2003-03-27 N- (2s)-4-(3,4-difluorobenzyl)morpholin-2-yl methyl -2- 3- (methylsulphonyl)amino phenyl acetamid als ccr3 antagonist für die behandlung von entzündlichen erkrankungen

Country Status (22)

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

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2003275257A1 (en) 2002-09-26 2004-04-19 Bristol-Myers Squibb Company N-substituted heterocyclic amines as modulators of chemokine receptor activity
JP2009501792A (ja) * 2005-07-21 2009-01-22 アストラゼネカ・アクチエボラーグ ケモカイン受容体のモジュレーターとしてのn−ベンジル−モルホリン誘導体
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
CA2623317A1 (en) * 2005-09-22 2007-03-29 Sanofi-Aventis Amino-alkyl-amide derivatives as ccr3 receptor liquids
HUP0800478A2 (en) * 2008-07-31 2010-03-01 Sanofi Aventis Substituted pyrrolidinyl-[1,3]thiazolo[4,5-b]pyridin derivatives as ccr3 receptor ligands
CN104203231A (zh) * 2011-12-01 2014-12-10 葛兰素集团有限公司 治疗和预防眼疾病的方法

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
US4870074A (en) * 1986-04-30 1989-09-26 Dainippon Pharmaceutical Co., Ltd. Substituted benzamide derivatives, for enhancing gastrointestinal motility
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 (enExample) * 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
EP1140834A1 (en) * 1998-12-18 2001-10-10 Du Pont Pharmaceuticals Company Heterocyclic piperidines as modulators of chemokine receptor activity
CA2383327C (en) * 1999-09-14 2009-11-03 Aventis Pharmaceuticals Inc. Thienoisoxazole phenoxy unsubstituted ethyl and propyl derivatives useful as d4 antagonists
BR0114323A (pt) * 2000-09-29 2003-07-01 Glaxo Group Ltd Composto ou um seu sal ou solvato farmaceuticamente aceitável, composição farmacêutica, uso do composto ou de um seu sal ou solvato farmaceuticamente aceitável, método de tratamento ou profilaxia de doenças inflamatórias, e, processo para preparar o composto
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

Also Published As

Publication number Publication date
CA2479910A1 (en) 2003-10-09
JP2005525390A (ja) 2005-08-25
ES2339436T3 (es) 2010-05-20
AU2003216905A1 (en) 2003-10-13
CN1642553A (zh) 2005-07-20
IS7415A (is) 2004-08-19
EP1487453A1 (en) 2004-12-22
MXPA04009458A (es) 2005-07-27
KR20040095347A (ko) 2004-11-12
IL163648A0 (en) 2005-12-18
BR0308719A (pt) 2005-01-04
TW200400823A (en) 2004-01-16
DE60330952D1 (de) 2010-03-04
GB0207449D0 (en) 2002-05-08
NO20044098L (no) 2004-10-04
EP1487453B1 (en) 2010-01-13
WO2003082291A1 (en) 2003-10-09
PL372930A1 (en) 2005-08-08
AR039177A1 (es) 2005-02-09
US20060058299A1 (en) 2006-03-16
RU2004126145A (ru) 2005-06-27
JP4490110B2 (ja) 2010-06-23
ZA200406990B (en) 2005-11-08

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