首页> 外国专利> Preparation method of 4 - (1 - hydroxy - (1-methylethyl) furan-2 sulfonamide by reaction with a Grignard Reagent and an ester Group is transformed into Alcohol in an Inert SolventThe reaction Intermediates, The Compound is useful in the synthesis of Derivatives of sulfonylurea inhibitors of interleukin 1.

Preparation method of 4 - (1 - hydroxy - (1-methylethyl) furan-2 sulfonamide by reaction with a Grignard Reagent and an ester Group is transformed into Alcohol in an Inert SolventThe reaction Intermediates, The Compound is useful in the synthesis of Derivatives of sulfonylurea inhibitors of interleukin 1.

机译:与格氏试剂反应并在惰性溶剂中将酯基转化为醇的方法制备4-(1-羟基-(1-甲基乙基)呋喃-2磺酰胺的方法中间体反应,该化合物可用于合成磺脲类抑制剂白介素1。

摘要

Method for preparing Furan sulfonamide compounds of Formula 1 comprising reacting a compound of formual IIWith a reacctivo Grignard reaction in an Inert Solvent to, where r is alkyl (C1 - C6).The Invention also includes compuestosintermediarios formula in which R is alkyl (C1 - C6) and q is Halo, Hydroxy or amino.The Compound of formula I are useful in the synthesis of inhibitors of interleukin 1.
机译:制备式1的呋喃磺酰胺化合物的方法,该方法包括使式II的化合物与惰性溶剂中的reacctivo Grignard反应在其中为r为烷基(C1-C6)的条件下反应。本发明还包括其中R为烷基(C1-C6)的中间中间体分子式。 C6),q为Halo,羟基或氨基。式I化合物可用于合成白介素1的抑制剂。

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