新产品编号:141307
Chemical Name: 4-(2-Methyl-4-phenylthiazol-5-yl)benzenesulfonamide
CAS No. 177560-71-3
项目整合开发状态: Preclinical
项目研究机构: Pfizer (Originator)
合成路线:The condensation of 4-(methylsulfanyl)benzaldehyde (I) with 4-fluorophenylacetic acid (II) in refluxing acetic anhydride containing one equivalent of triethylamine,followed by aqueous hydrolysis,provided the diarylpropenoic acid (III).Curtius rearrangement of acid (III) by treatment with diphenylphosphoryl azide in cold toluene,and subsequent hydrolysis of the intermediate isocyanate afforded diarylethanone (IV),which was then brominated in a solution of HBr in acetic acid to give bromoketone (V).The cyclization of this bromoketone with 2-chlorothiobenzamide (VI) in refluxing acetonitrile gave rise to thiazole (VII),and then,oxidation with meta-chloroperbenzoic acid in dichloromethane provided the target sulfone.
合成路线:Treatment of benzoin (I) with methanesulfonyl chloride and LiCl,followed by condensation with thioacetamide afforded 2-methyl-3,4-diphenylthiazole (II).Subsequent selective chlorosulfonation at the most reactive 5-phenyl group of (II) provided sulfonyl chloride (III).This was finally converted to the target sulfonamide upon treatment with ammonium hydroxide.
📌 参考资料/链接:
参考文献标题:Substd.thiazoles for the treatment of inflammation
文献作者:Talley,J.J.; Carter,J.S.; Collins,P.W.; Kramer,S.W.; Penning,T.D.; Rogier,D.J.Jr.; Rogers,R.S.(Pharmacia Corp.)
参考来源:EP 0772606; JP 1998504542; US 5668161; WO 9603392
📄 详细内容
合成路线:Treatment of benzoin (I) with methanesulfonyl chloride and LiCl,followed by condensation with thioacetamide afforded 2-methyl-3,4-diphenylthiazole (II).Subsequent selective chlorosulfonation at the most reactive 5-phenyl group of (II) provided sulfonyl chloride (III).This was finally converted to the target sulfonamide upon treatment with ammonium hydroxide.
参考文献标题:Synthesis and activity of sulfonamide-substituted 4,5-diaryl thiazoles as selective cyclooxygenase-2 inhibitors
文献作者:Carter,J.S.; Kramer,S.; Talley,J.J.; Penning,T.; Collins,P.; Graneto,M.J.; Seibert,K.; Koboldt,C.M.; Masferrer,J.; Zweifel,B.
参考来源:Bioorg Med Chem Lett 1999,9(8),1171