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HRID 4961作成日:2026年10月25日

Nitrogen → 6-[4-(4-(5-Hydroxymethylbenzimidazol-1-yl)butyl)piperazino]-1,4-benzodioxane

https://huagongshe.com/reaction/4961

反応式

関与物質

役割名称HCID仕込み量
反応物NitrogenHCID 947—
反応物Sodium HydroxideHCID 14798—
反応物6-[4-(4-(5-Methoxycarbonylbenzimidazol-1-yl)butyl)piperazino]-1,4-benzodioxaneHCID 19797327—
反応物Aluminium lithium hydrideHCID 21226445—
溶媒TetrahydrofuranHCID 8028—
生成物6-[4-(4-(5-Hydroxymethylbenzimidazol-1-yl)butyl)piperazino]-1,4-benzodioxaneHCID 19797328—

反応手順

A solution of 4.4 g of 6-[4-(4-(5-methoxycarbonylbenzimidazol-1-yl)butyl)piperazino]-1,4-benzodioxane in 40 ml of THF is added dropwise with stirring in an N2 atmosphere at 20° to a suspension of 0.6 g of lithium aluminium hydride in 20 ml of THF. The mixture is stirred at 20° for 1 hour, decomposed with dilute sodium hydroxide solution and filtered, and the filtrate is worked up in the conventional manner and gives 6-[4-(4-(5-hydroxymethylbenzimidazol-1-yl)butyl)piperazino]-1,4-benzodioxane.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05242925
出典データセットuspto-grants-1993_09
ORD IDord-22a8f936264443019aa427698e2e3d90
出典メモuspto-grants-1993_09