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NO312461B1 - Krystallinsk form B av 4-[5-metyl-3-fenylisoksazol-4- yl]benzensulfonamid - Google Patents

Krystallinsk form B av 4-[5-metyl-3-fenylisoksazol-4- yl]benzensulfonamid Download PDF

Info

Publication number
NO312461B1
NO312461B1 NO19990541A NO990541A NO312461B1 NO 312461 B1 NO312461 B1 NO 312461B1 NO 19990541 A NO19990541 A NO 19990541A NO 990541 A NO990541 A NO 990541A NO 312461 B1 NO312461 B1 NO 312461B1
Authority
NO
Norway
Prior art keywords
methyl
phenylisoxazol
benzenesulfonamide
treatment
crystalline form
Prior art date
Application number
NO19990541A
Other languages
English (en)
Norwegian (no)
Other versions
NO990541L (no
NO990541D0 (no
Inventor
John J Talley
John R Medich
Kathleen T Mclaughlin
Henry T Gaud
Edward E Yonan
Original Assignee
Searle & Co
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 Searle & Co filed Critical Searle & Co
Publication of NO990541L publication Critical patent/NO990541L/no
Publication of NO990541D0 publication Critical patent/NO990541D0/no
Publication of NO312461B1 publication Critical patent/NO312461B1/no

Links

Classifications

    • H10W40/611—
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/42—Oxazoles
    • 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
    • A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
    • C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
    • C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
    • C07D261/08—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • H10W40/73—

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Rheumatology (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Pain & Pain Management (AREA)
  • Neurosurgery (AREA)
  • Immunology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Epidemiology (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Physics & Mathematics (AREA)
  • Condensed Matter Physics & Semiconductors (AREA)
  • General Physics & Mathematics (AREA)
  • Computer Hardware Design (AREA)
  • Microelectronics & Electronic Packaging (AREA)
  • Power Engineering (AREA)
  • Liquid Crystal Substances (AREA)
  • Heat Sensitive Colour Forming Recording (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
NO19990541A 1996-08-14 1999-02-05 Krystallinsk form B av 4-[5-metyl-3-fenylisoksazol-4- yl]benzensulfonamid NO312461B1 (no)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US2437896P 1996-08-14 1996-08-14
PCT/US1997/015126 WO1998006708A1 (en) 1996-08-14 1997-08-12 Crystalline form of 4-[5-methyl-3-phenylisoxazol-4-yl]benzenesulfonamide

Publications (3)

Publication Number Publication Date
NO990541L NO990541L (no) 1999-02-05
NO990541D0 NO990541D0 (no) 1999-02-05
NO312461B1 true NO312461B1 (no) 2002-05-13

Family

ID=21820280

Family Applications (1)

Application Number Title Priority Date Filing Date
NO19990541A NO312461B1 (no) 1996-08-14 1999-02-05 Krystallinsk form B av 4-[5-metyl-3-fenylisoksazol-4- yl]benzensulfonamid

Country Status (38)

Country Link
US (2) US6441014B2 (is)
EP (2) EP1283203A1 (is)
JP (2) JP3631763B2 (is)
KR (1) KR100383148B1 (is)
CN (1) CN1205193C (is)
AP (1) AP1055A (is)
AR (1) AR009244A1 (is)
AT (1) ATE228117T1 (is)
AU (1) AU722072B2 (is)
BG (1) BG64259B1 (is)
BR (1) BR9711151A (is)
CA (1) CA2264104A1 (is)
CZ (1) CZ297679B6 (is)
DE (1) DE69717281T2 (is)
DK (1) DK0920422T3 (is)
EA (2) EA001472B1 (is)
EE (1) EE04237B1 (is)
ES (1) ES2188971T3 (is)
GE (1) GEP20022636B (is)
HU (1) HUP0400923A3 (is)
IL (2) IL128255A (is)
IS (1) IS1989B (is)
LT (1) LT4551B (is)
LV (1) LV12274B (is)
NO (1) NO312461B1 (is)
NZ (1) NZ334132A (is)
OA (1) OA11298A (is)
PL (1) PL191313B1 (is)
PT (1) PT920422E (is)
RO (1) RO120771B1 (is)
RS (1) RS49671B (is)
SI (1) SI9720059B (is)
SK (1) SK283558B6 (is)
TR (1) TR199900298T2 (is)
TW (1) TW527350B (is)
UA (1) UA52684C2 (is)
WO (1) WO1998006708A1 (is)
ZA (1) ZA977314B (is)

Families Citing this family (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DK0920422T3 (da) * 1996-08-14 2003-03-17 Searle & Co Krystallinsk form af 4-[5-methyl-3-phenylisoxazol-4-yl]benzensulfonamid
US6887893B1 (en) * 1997-12-24 2005-05-03 Sankyo Company, Limited Methods and compositions for treatment and prevention of tumors, tumor-related disorders and cachexia
GB9810920D0 (en) * 1998-05-21 1998-07-22 Merck Sharp & Dohme Therapeutic use
JP2002522425A (ja) * 1998-08-07 2002-07-23 カイロン コーポレイション エストロゲンレセプターモジュレーターとしての置換イソオキサゾール
AU1398899A (en) * 1998-11-12 2000-06-05 Algos Pharmaceutical Corporation Cox-2 inhibitors in combination with centrally acting analgesics
EP1156855A1 (en) * 1999-03-01 2001-11-28 Ortho-McNeil Pharmaceutical, Inc. Composition comprising a tramadol material and a selective cox-2 inhibitor drug
MXPA02001820A (es) 1999-08-20 2003-07-14 Johnson & Johnson Composicion que comprende un material de tramadol y un farmaco anticonvulsivo.
WO2001015687A1 (en) * 1999-08-27 2001-03-08 Merck & Co., Inc. Method for treating or preventing chronic prostatitis or chronic pelvic pain syndrome
EP1175214B1 (en) 1999-12-08 2004-11-24 Pharmacia Corporation Cyclooxygenase-2 inhibitor compositions having rapid onset of therapeutic effect
DE10032132A1 (de) * 2000-07-01 2002-01-17 Lohmann Therapie Syst Lts Dermales Therapeutisches System enthaltend nichtsteroidale Antiphlogistika mit selektiver COX-2-Hemmung
AR038957A1 (es) 2001-08-15 2005-02-02 Pharmacia Corp Terapia de combinacion para el tratamiento del cancer
DK3168218T3 (en) * 2001-08-15 2019-01-14 Pharmacia & Upjohn Co Llc Crystalline comprising an L-malic acid salt of N- [2- (DIETHYLAMINO) ETHYL] -5 - [(5-FLUOR-1,2-DIHYDRO-2-OXO-3H-INDOL-3-YLIDE) METHYL] -2,4 -DIMETHYL-1H-PYRROL-3-CARBOXAMIDE FOR USE AS A MEDICINE
US20070072921A1 (en) * 2002-07-26 2007-03-29 Talley John J Crystalline form of 4-[5-methyl-3-phenylisoxazol-4-yl] benzenesulfonamide
US7538126B2 (en) 2003-04-04 2009-05-26 Hetero Drugs Limited Crystalline forms of valdecoxib
PL2266585T3 (pl) 2003-05-07 2013-10-31 Osteologix As Rozpuszczalne w wodzie sole stronktu do stosowania w leczeniu chorób chrząstki i/lub kości
US20050182113A1 (en) * 2003-12-30 2005-08-18 Venkataraman Sundaram Method for preparing diaryl-substituted isoxazole compounds
US20050272787A1 (en) * 2004-05-19 2005-12-08 Eswaraiah Sajja Process for preparing crystalline form A of valdecoxib
WO2005120499A1 (en) * 2004-06-10 2005-12-22 Chandiran Thakashinamoorthy Form a of valdecoxib suitable for pharmaceutical formulations
MY147767A (en) 2004-06-16 2013-01-31 Janssen Pharmaceutica Nv Novel sulfamate and sulfamide derivatives useful for the treatment of epilepsy and related disorders
ATE368639T1 (de) * 2004-06-28 2007-08-15 Gruenenthal Gmbh Kristalline formen von (-)-(1r,2r)-3-(3- dimethylamino-1-ethyl-2-methylpropyl)-phenol hydrochlorid
KR100591786B1 (ko) 2004-10-19 2006-06-26 휴먼팜 주식회사 프란루카스트를 함유하는 약학적 조성물 및 이의 제조 방법
EP1881959A1 (en) 2005-05-20 2008-01-30 Janssen Pharmaceutica N.V. Process for preparation of sulfamide derivatives
US8937096B2 (en) 2005-12-19 2015-01-20 Janssen Pharmaceutica Nv Use of benzo-fused heterocyle sulfamide derivatives for the treatment of mania and bipolar disorder
US8492431B2 (en) 2005-12-19 2013-07-23 Janssen Pharmaceutica, N.V. Use of benzo-fused heterocycle sulfamide derivatives for the treatment of obesity
US8497298B2 (en) 2005-12-19 2013-07-30 Janssen Pharmaceutica Nv Use of benzo-fused heterocycle sulfamide derivatives for lowering lipids and lowering blood glucose levels
US8691867B2 (en) 2005-12-19 2014-04-08 Janssen Pharmaceutica Nv Use of benzo-fused heterocycle sulfamide derivatives for the treatment of substance abuse and addiction
US8716231B2 (en) 2005-12-19 2014-05-06 Janssen Pharmaceutica Nv Use of benzo-fused heterocycle sulfamide derivatives for the treatment of pain
AU2007253814A1 (en) 2006-05-19 2007-11-29 Janssen Pharmaceutica N.V. Co-therapy for the treatment of epilepsy
WO2010008776A2 (en) 2008-06-23 2010-01-21 Janssen Pharmaceutica Nv Disposable patch and reusable sensor assembly for use in medical device localization and mapping systems
US8815939B2 (en) 2008-07-22 2014-08-26 Janssen Pharmaceutica Nv Substituted sulfamide derivatives
CN103172583A (zh) * 2013-03-07 2013-06-26 深圳市资福药业有限公司 一种制备帕瑞昔布的方法
US9375417B2 (en) 2014-12-04 2016-06-28 Mary's Medicinals LLC Transdermal cannabinoid formulations
US10028904B2 (en) 2014-12-04 2018-07-24 Wisconsin Alumni Research Foundation Transdermal cannabinoid formulations
CN114441666B (zh) * 2020-11-05 2024-02-27 成都百裕制药股份有限公司 一种4-(5-甲基-3-苯基-4-异恶唑)苯磺酰氯中杂质的检测方法
CA3209491A1 (en) 2021-03-15 2022-09-22 Saul Yedgar Hyaluronic acid-conjugated dipalmitoyl phosphatidyl ethanolamine in combination with non-steroidal anti-inflammatory drugs (nsaids) for treating or alleviating inflammatory disease

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5474995A (en) * 1993-06-24 1995-12-12 Merck Frosst Canada, Inc. Phenyl heterocycles as cox-2 inhibitors
US5633272A (en) 1995-02-13 1997-05-27 Talley; John J. Substituted isoxazoles for the treatment of inflammation
ES2183935T3 (es) * 1995-02-13 2003-04-01 Searle & Co Isoxazoles sustituidos para el tratamiento de la inflamacion.
US5643933A (en) 1995-06-02 1997-07-01 G. D. Searle & Co. Substituted sulfonylphenylheterocycles as cyclooxygenase-2 and 5-lipoxygenase inhibitors
DK0920422T3 (da) * 1996-08-14 2003-03-17 Searle & Co Krystallinsk form af 4-[5-methyl-3-phenylisoxazol-4-yl]benzensulfonamid
US7538126B2 (en) * 2003-04-04 2009-05-26 Hetero Drugs Limited Crystalline forms of valdecoxib
US20050272787A1 (en) * 2004-05-19 2005-12-08 Eswaraiah Sajja Process for preparing crystalline form A of valdecoxib

Also Published As

Publication number Publication date
NO990541L (no) 1999-02-05
RS49671B (sr) 2007-11-15
OA11298A (en) 2003-10-22
WO1998006708A1 (en) 1998-02-19
JP2005015497A (ja) 2005-01-20
KR20000029994A (ko) 2000-05-25
YU7499A (sh) 2000-03-21
US20030004200A1 (en) 2003-01-02
KR100383148B1 (ko) 2003-05-09
ES2188971T3 (es) 2003-07-01
LV12274B (en) 1999-09-20
AU722072B2 (en) 2000-07-20
EE9900053A (et) 1999-08-16
SI9720059B (sl) 2011-11-30
US6441014B2 (en) 2002-08-27
SK283558B6 (sk) 2003-09-11
US20010003752A1 (en) 2001-06-14
HUP0400923A2 (hu) 2004-08-30
DK0920422T3 (da) 2003-03-17
RO120771B1 (ro) 2006-07-28
UA52684C2 (uk) 2003-01-15
EA001472B1 (ru) 2001-04-23
IL128255A0 (en) 1999-11-30
ZA977314B (en) 1998-08-14
SK13699A3 (en) 1999-07-12
IL128255A (en) 2004-06-20
BR9711151A (pt) 1999-08-17
EA200000891A1 (ru) 2001-02-26
LV12274A (lv) 1999-05-20
AU4093697A (en) 1998-03-06
CZ297679B6 (cs) 2007-03-07
NO990541D0 (no) 1999-02-05
EE04237B1 (et) 2004-02-16
DE69717281T2 (de) 2003-09-04
EA003754B1 (ru) 2003-08-28
EP0920422B1 (en) 2002-11-20
EP0920422A1 (en) 1999-06-09
CN1233243A (zh) 1999-10-27
HUP0400923A3 (en) 2007-11-28
LT99024A (en) 1999-07-26
US7135489B2 (en) 2006-11-14
AP9901458A0 (en) 1999-03-31
PT920422E (pt) 2003-03-31
DE69717281D1 (de) 2003-01-02
JP2000506542A (ja) 2000-05-30
EP1283203A1 (en) 2003-02-12
CZ33499A3 (cs) 1999-06-16
IS1989B (is) 2005-02-15
AP1055A (en) 2002-04-04
AR009244A1 (es) 2000-04-12
TR199900298T2 (xx) 1999-05-21
LT4551B (lt) 1999-10-25
ATE228117T1 (de) 2002-12-15
EA199900200A1 (ru) 1999-06-24
CN1205193C (zh) 2005-06-08
SI9720059A (sl) 1999-12-31
IS4961A (is) 1999-01-29
PL191313B1 (pl) 2006-04-28
GEP20022636B (en) 2002-02-25
IL161224A0 (en) 2004-09-27
CA2264104A1 (en) 1998-02-19
HK1023125A1 (en) 2000-09-01
BG103155A (bg) 1999-11-30
TW527350B (en) 2003-04-11
NZ334132A (en) 2000-06-23
BG64259B1 (bg) 2004-07-30
JP3631763B2 (ja) 2005-03-23
PL331607A1 (en) 1999-08-02

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