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HRID 1006421作成日:2026年10月24日

t-butyl 4-(1-benzenesulfonyl-1H-indol-4-yl)piperazine-1-carboxylate → 1-(Phenylsulfonyl)-4-(1-piperazinyl)-1h-indole

https://huagongshe.com/ja/reaction/1006421

反応式

関与物質

役割名称HCID仕込み量
反応物t-butyl 4-(1-benzenesulfonyl-1H-indol-4-yl)piperazine-1-carboxylateHCID 22015366—
溶媒Trifluoroacetic acidHCID 6422—
生成物1-(Phenylsulfonyl)-4-(1-piperazinyl)-1h-indoleHCID 10154392—

反応手順

A solution of 125 mg (0.28 mmole) 4-(1-benzenesulfonyl-1H-indol-4-yl)-piperazine-1-carboxylic acid tert-butyl ester in 2 mL trifluoroacetic acid was stored at room temperature for 10 minutes. The solution was concentrated under reduced pressure and the residue was partitioned between 3 mL 10% sodium carbonate and 20 mL ethyl acetate. The organic phase was washed with 5 mL water, dried (magnesium sulfate) and concentrated. 1-Benzenesulfonyl-4-piperazin-1-yl-1H-indole (5) was isolated as the hydrochloride salt from ethyl acetate-ethyl ether, 73 mg, M+H=342; m.p.294-295° 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-739071936fc645228785cdc460a703e5
出典メモuspto-grants-2004_09