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HRID 66302作成日:2026年10月26日

Triethylamine → N-{1-[2-(1H-Indol-3-yl)ethyl]piperidin-4-yl}methanesulfonamide

https://huagongshe.com/reaction/66302

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Methanesulfonyl chlorideHCID 31297—
反応物4-Piperidinamine, 1-(2-(1H-indol-3-yl)ethyl)-, hydrateHCID 215415—
溶媒DichloromethaneHCID 6344—
生成物N-{1-[2-(1H-Indol-3-yl)ethyl]piperidin-4-yl}methanesulfonamideHCID 22754838105.7%

反応手順

To 3-[2-(4-Amino-1-piperidyl)ethyl]indole (1.307 g.) suspended in a solution of triethylamine (2 mls.) in dichloromethane (10 mls.) at room temperature with stirring was added methane sulphonyl chloride (0.570 g.) in dichloromethane (5 mls.). After stirring for 18 hours the solution was washed with water and the organic phase separated, dried and evaporated to yield the title compound (1.690 g.) as an oil. This was recrystallized from ethanolic hydrogen chloride as the hydrochloride salt (0.560 g., m.p. 241°-242° C.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04131680
出典データセットuspto-grants-1978_12
ORD IDord-945371300be648fc962154efaeb99079
出典メモuspto-grants-1978_12