돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1428952생성일: 2026년 10월 26일

Triethylamine → N-Cyclopropyl-N-piperidin-4-yl-3-(trifluoromethyl)benzenesulfonamide

https://huagongshe.com/reaction/1428952

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Potassium CarbonateHCID 11430—
반응물3-(Trifluoromethyl)benzenesulfonyl chlorideHCID 2733250—
반응물1-Benzyl-N-cyclopropylpiperidin-4-amineHCID 2735481—
반응물N-(1-benzylpiperidin-4-yl)-N-cyclopropyl-3-trifluoromethyl-benzenesulfonamideHCID 4114155—
용매DichloromethaneHCID 6344—
생성물N-Cyclopropyl-N-piperidin-4-yl-3-(trifluoromethyl)benzenesulfonamideHCID 2773944—
생성물N-(1-benzylpiperidin-4-yl)-N-cyclopropyl-3-trifluoromethyl-benzenesulfonamideHCID 4114155—

반응 단계

N-(1-Benzylpiperidin-4-yl)-N-cyclopropyl-3-trifluoromethyl-benzenesulfonamide: N-Benzyl-4-cyclopropylaminopiperidine (5.0 g, 21.71 mmol) and triethylamine (3.6 mL, 26.05 mmol) were dissolved in dichloromethane (DCM, 100 mL). 3-Trifluoromethylbenzenesulfonyl chloride (3.47 mL, 21.71 mmol) was added and the resulting reaction mixture was stirred overnight. The mixture then was poured into potassium carbonate solution (200 mL), extracted with ether (2×200 mL), dried (MgSO4), and concentrated in vacuum to give a crude product as a yellow gum, which was purified by column chromatography on silica gel (hexane/EtOAc, 2:1). The title compound N-(1-benzylpiperidin-4-yl)-N-cyclopropyl-3-trifluoromethyl-benzenesulfonamide was obtained (9 g, 95% yield) as a pale yellow gum. Rf=0.42 (UV detection).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08937181B2
출처 데이터셋uspto-grants-2015_01
ORD IDord-1f6641ea8fe248938efe7100e90267a5
출처 메모uspto-grants-2015_01