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HRID 1006420作成日:2026年10月27日

Benzenesulfonyl chloride → t-butyl 4-(1-benzenesulfonyl-1H-indol-4-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1006420

反応式

関与物質

役割名称HCID仕込み量
反応物Benzenesulfonyl chlorideHCID 7369—
反応物tert-Butyl 4-(1H-indol-4-yl)piperazine-1-carboxylateHCID 22015386—
触媒Tetrabutylammonium hydrogen sulfateHCID 94433—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
溶媒Sodium HydroxideHCID 14798—
生成物t-butyl 4-(1-benzenesulfonyl-1H-indol-4-yl)piperazine-1-carboxylateHCID 22015366—

反応手順

A mixture of 165 mg (0.55 mmole) 4-(1H-indol-4-yl)-piperazine-1-carboxylic acid tert-butyl ester, 25 mg tetrabutylammonium hydrogen sulfate and 0.08 mL (0.6 mmole) benzenesulfonyl chloride in 2 mL 4 M sodium hydroxide and 5 mL toluene was stirred at room temperature for 2 hours. The mixture was diluted with 5 mL water and extracted with 25 mL ethyl acetate. The organic phase was washed with 5 mL water, 5 mL saturated sodium chloride, dried (magnesium sulfate) and concentrated. 4-(1-Benzenesulfonyl-1H-indol-4-yl)-piperazine-1-carboxylic acid tert-butyl ester was isolated by recrystallization from ether/hexane, 223 mg, m.p. 143-144° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06790848B2
出典データセットuspto-grants-2004_09
ORD IDord-079b97bf846441cc836cfa9bcbc885ff
出典メモuspto-grants-2004_09