DuP-991
Chemical Name: 3-(2-Chlorophenyl)-2-(2,4-difluorophenyl)-1-(1H-1,2,4-triazol-1-yl)-3-buten-2-ol methanesulfonate
项目整合开发状态: Preclinical
项目研究机构: BTG (Technology Transfer), Bristol-Myers Squibb (Originator)
合成路线:This compound can be obtained by two related ways:1) The reaction of alpha-bromo-2-chlorostyrene (I) with magnesium gives the corresponding magnesiane (II),which is condensed with alpha,4-dichloroacetophenone (III) yielding 3-(2-chlorophenyl-2-(4-chlorophenyl)-1,2-epoxy-3-butene (IV).Finally,this compound is treated with potassium 1,2,4-triazole (V).2) The reaction of 1-(2-chlorophenyl)-2-(4-chlorophenyl)-2,3-epoxy-1-propane (VI) with methyltriphenylphosphonium bromide and n-butyllithium gives epoxide (IV),already obtained.
合成路线:The intermediate epoxide (IV) was synthesized by two different procedures:1) The Grignard reagent (II),prepared from 1-bromo-2'-chlorostyrene (I) and Mg,was condensed with 2-chloro-2',4'-difluoroacetophenone (III) to afford epoxide (IV).2) Alternatively,Wittig reaction of epoxyketone (V) with methylenetriphenylphosphorane provided the target intermediate (IV).The title compound was then obtained by epoxide opening of (IV) with potassium triazole (VI) in DMF at 60 C,and was isolated as the methanesulfonate salt.
📌 参考资料/链接:
参考文献标题:Antifungal carbinols
文献作者:Cuomo,J.; Greenberg,R.S.; Olson,R.E.(DuPont Pharmaceuticals Co.)
参考来源:EP 0251086; JP 1988060975