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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 258712생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/258712

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methanesulfonyl chlorideHCID 31297—
반응물4-Piperidinamine, 1-(2-(1H-indol-3-yl)ethyl)-, hydrateHCID 215415—
용매DichloromethaneHCID 6344—
생성물N-{1-[2-(1H-Indol-3-yl)ethyl]piperidin-4-yl}methanesulfonamideHCID 22754838105.7%

반응 단계

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 recrystallised from ethanolic hydrogen chloride as the hydrochloride salt (0.560 g., m.p. 241°-242° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04034098
출처 데이터셋uspto-grants-1977_07
ORD IDord-1c0fc56b21124a86b1764bb51ba8f5f9
출처 메모uspto-grants-1977_07