TW200616983A - Method for preparation of diarylisoxazole sulfonamide compounds and intermediates - Google Patents

Method for preparation of diarylisoxazole sulfonamide compounds and intermediates

Info

Publication number
TW200616983A
TW200616983A TW094119537A TW94119537A TW200616983A TW 200616983 A TW200616983 A TW 200616983A TW 094119537 A TW094119537 A TW 094119537A TW 94119537 A TW94119537 A TW 94119537A TW 200616983 A TW200616983 A TW 200616983A
Authority
TW
Taiwan
Prior art keywords
compound
diarylisoxazole
diaryl
diarylenamine
contacting
Prior art date
Application number
TW094119537A
Other languages
Chinese (zh)
Inventor
Leo J Letendre
Cynthia K Snoddy
George H Klemm
Jon P Lawson
Michael J Bauer
Original Assignee
Pharmacia Corp
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 Pharmacia Corp filed Critical Pharmacia Corp
Publication of TW200616983A publication Critical patent/TW200616983A/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D261/00Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
    • C07D261/02Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
    • C07D261/04Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D261/00Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
    • C07D261/02Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
    • C07D261/06Heterocyclic 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
    • C07D261/08Heterocyclic 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Abstract

The disclosure provides a method for the preparation of a diarylisoxazole sulfonamide compound comprising contacting a deoxybenzoin with a secondary amine to form a diarylenamine compound; contacting the diarylenamine compound with an acetylating agent to form an acetyl diarylenamine compound; contacting the acetyl diarylenamine compound with a source of hydroxylamine to form an diaryl isoxazolol compound; eliminating water from the diaryl isoxazolol compound to form a diaryl isoxazole compound, chlorosulfonating the diarylisoxazole compound to form a chlorosulfonyl diaryl isoxazole compound; and contacting the chlorosulfonyl diaryl isoxazole compound with a source of ammonia to form the diarylisoxazole sulfonamide compound.
TW094119537A 2004-06-14 2005-06-13 Method for preparation of diarylisoxazole sulfonamide compounds and intermediates TW200616983A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US57959104P 2004-06-14 2004-06-14

Publications (1)

Publication Number Publication Date
TW200616983A true TW200616983A (en) 2006-06-01

Family

ID=34972271

Family Applications (1)

Application Number Title Priority Date Filing Date
TW094119537A TW200616983A (en) 2004-06-14 2005-06-13 Method for preparation of diarylisoxazole sulfonamide compounds and intermediates

Country Status (3)

Country Link
AR (1) AR049301A1 (en)
TW (1) TW200616983A (en)
WO (1) WO2005123701A1 (en)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103172583A (en) * 2013-03-07 2013-06-26 深圳市资福药业有限公司 Parecoxib preparation method
CN104250232A (en) * 2013-06-26 2014-12-31 四川唯拓生物医药有限公司 Preparation method of parecoxib sodium
CN104447600B (en) * 2013-09-22 2016-03-30 江苏奥赛康药业股份有限公司 A kind of Preparation Method And Their Intermediate impurity of Parecoxib sodium compound, preparation method and application
CN105085425B (en) * 2014-05-23 2018-01-30 昆药集团股份有限公司 A kind of method for preparing SC 69124
CN104193694B (en) * 2014-09-19 2016-08-24 成都欣捷高新技术开发有限公司 A kind of method preparing Parecoxib Sodium intermediate
CN105801508B (en) * 2014-12-30 2018-12-11 上海鼎雅药物化学科技有限公司 The preparation method of SC 69124
CN106146424A (en) * 2015-03-23 2016-11-23 上海医药工业研究院 A kind of preparation method of 5-methyl-3,4-diphenyl isoxazole
CN105418528B (en) * 2015-12-31 2018-08-24 山东罗欣药业集团股份有限公司 A kind of preparation method of Parecoxib Sodium
CN106008386B (en) * 2016-05-25 2018-11-06 台州宝诚科技服务有限公司 A method of preparing the SC 69124 for treating postoperative pain
CN106008388B (en) * 2016-05-25 2018-06-26 吴兴龙 A kind of preparation method for the SC 69124 for being used to treat postoperative pain
CN110305071A (en) * 2019-07-23 2019-10-08 成都通德药业有限公司 A kind of synthetic method of Parecoxib Sodium intermediate SC 69124
CN110790745A (en) * 2019-11-12 2020-02-14 青岛科技大学 Preparation method for extracting vitacoxib from waste tablets
CN111153865A (en) * 2020-01-19 2020-05-15 上海臣邦医药科技股份有限公司 Parecoxib sodium substituted impurity and preparation method thereof
CN111153866A (en) * 2020-01-19 2020-05-15 上海臣邦医药科技股份有限公司 Parecoxib sodium disubstituted impurity and preparation method and application thereof

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU699593B2 (en) * 1995-02-13 1998-12-10 G.D. Searle & Co. Substituted isoxazoles for the treatment of inflammation
US6673818B2 (en) * 2001-04-20 2004-01-06 Pharmacia Corporation Fluoro-substituted benzenesulfonyl compounds for the treatment of inflammation

Also Published As

Publication number Publication date
AR049301A1 (en) 2006-07-12
WO2005123701A1 (en) 2005-12-29

Similar Documents

Publication Publication Date Title
TW200616983A (en) Method for preparation of diarylisoxazole sulfonamide compounds and intermediates
EA200900636A1 (en) COMPOUNDS OF OXASOLIDINE AND THEIR APPLICATION AS HYDRATES INHIBITORS
WO2007030582A3 (en) Acyclic ikur inhibitors
CL2008001896A1 (en) 3-dihalomethyl-1-methyl-1h-pyrazole-4-carbaldehydes; its preparation process using a hydrazone intermediate, which reacts with a vilsmeier agent; and the hydrazone derivative used.
UY31502A1 (en) IMPROVED PROCESS TO SYNTHEIZE 5-CYCLOPENTYL-5-11-DIHYDRO-10-OXA-1-AZA-DIBENZO [A, D] CYCLOHEPTEN-5-OL USING TMEDA
WO2008024535A3 (en) Exhaust aftertreatment system with spiral mixer
TW200740761A (en) Histone deacetylase inhibitors
MY162760A (en) Anti-infective agents and uses thereof
EA200701191A1 (en) TENSIONERS WITH COATING FROM DISPERTOR
TW200732836A (en) Method for expelling gas positioned between a substrate and a mold
NO20074404L (en) Microcrystalline (5-fluoro-2-methyl-3-quinolin-2-ylmethyl-indol-1-yl) acetic acid
WO2006122319A3 (en) Histone deacetylase inhibitors
WO2007109365A3 (en) Process for the synthesis of arylamines from the reaction of an aromatic compound with ammonia or a metal amide
WO2007085514A3 (en) Method for producing methionine from homoserine
NO20081684L (en) An improved process for the preparation of okazolidine-protecting amino-diol compounds useful as intermediates for Florfenicol
GEP20125512B (en) Process for synthesis of agomelatin
CL2012000114A1 (en) Process for the preparation of compounds derived from 5-amino-benzonorbornadiene where a compound of 5-halo-benzonorbornadiene is reacted with a benzylamine in the presence of a palladium catalyst.
EA200500202A1 (en) NEW METHOD OF SYNTHESIS (7-METHOXY-3,4-DIHYDRO-1-NAPHTHALINIL) ACETONITRILE AND ITS APPLICATION IN THE SYNTHESIS OF AGOMELATIN
WO2009074741A3 (en) Novel method for the synthesis of strontiuim ranelate and of hydrates thereof
WO2007062314A3 (en) Heterocyclic cetp inhibitors
MY176953A (en) Method for purifying gas mixtures containing mercaptans and other acid gases
TW200740769A (en) Novel process
EA200900008A1 (en) NEW CHIRAL INTERMEDIATE PRODUCTS, METHOD OF THEIR PRODUCTION AND THEIR APPLICATION IN THE PRODUCTION OF TLTERODINE, PHESOTORODINE OR THEIR ACTIVE METABOLITES
TW200628461A (en) Improved seal swell agent and process therefor
DK2265580T3 (en) Hitherto unknown method for the preparation of sulfonyl pyrrols as HDAC inhibitors