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HRID 1006418作成日:2026年10月27日

1-Chloroethyl chloroformate → 1-(3,5-Dichloro-benzenesulfonyl)-4-piperazin-1-yl-1H-indole

https://huagongshe.com/reaction/1006418

反応式

関与物質

役割名称HCID仕込み量
反応物1-Chloroethyl chloroformateHCID 521305—
反応物4-(4-benzyl-piperazin-1-yl)-1-(3,5-dichloro-benzenesulfonyl)-1H-indoleHCID 12137124—
溶媒1,2-DichloroethaneHCID 11—
生成物1-(3,5-Dichloro-benzenesulfonyl)-4-piperazin-1-yl-1H-indoleHCID 10223261—

反応手順

A solution of 0.1 g (0.2 mmole) 4-(4-benzyl-piperazin-1-yl)-1-(3,5-dichloro-benzenesulfonyl)-1H-indole and 0.05 mL (0.46 mmole) 1-chloroethyl chloroformate in 10 mL 1,2-dichloroethane was heated under reflux for 0.5 hour. The solution was concentrated under reduced pressure and the residue was dissolved in 6 mL methanol. The solution was heated under reflux for 1 hour, then it was concentrated. 1-(3,5-Dichloro-benzenesulfonyl)-4-piperazin-1-yl-1H-indole (2) was isolated as the hydrochloride salt from methanol/ethyl ether, 74 mg, M+H=410, m.p. 156-157° 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-25b87b6c49774dbea738442a5ddde63f
出典メモuspto-grants-2004_09