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HRID 883531作成日:2026年10月26日

Diisopropylethylamine → 3-Phenylsulfonyl-8-piperazin-1-yl-quinoline hydrochloride

https://huagongshe.com/reaction/883531

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物1-Chloroethyl chloroformateHCID 521305—
反応物8-(4-Methyl-piperazin-1-yl)-3phenylsulfonylquinolineHCID 9929162—
溶媒1,2-DichloroethaneHCID 11—
生成物3-Phenylsulfonyl-8-piperazin-1-yl-quinoline hydrochlorideHCID 5697214152.5%

反応手順

A stirred solution of 8-(4-methyl-piperazin-1-yl)-3-phenylsulfonylquinoline (E1) (0.148 g, 0.4 mmol), 1-chloroethyl chloroformate (0.093 ml, 0.85 mmol) and N,N-diisopropylethylamine (0.148 ml, 0.85 mmol) in 1,2-dichloroethane (9 ml) was heated at reflux for 1.25 h under argon. The reaction mixture was cooled to ambient temperature and concentrated in vacuo to an oil. The oil was purified by chromatography over silica gel eluting with a gradient of methanol/dichloromethane, pooling fractions which contained the major component (Rf 0.9, methanol/dichloromethane 1:19). The purified material was redissolved in methanol (15 ml) and the solution was refluxed for 1 h under argon. The reaction mixture was cooled to ambient temperature and concentrated in vacuo to a solid which was stirred with diethyl ether (5 ml) and filtered to afford the title compound (E2) (0.08 g, 0.21 mmol, 51%);

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08236947B2
出典データセットuspto-grants-2012_08
ORD IDord-3b50d8856611446ba3e29aa96b6acfa8
出典メモuspto-grants-2012_08