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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1610901생성일: 2026년 10월 26일

Triethylamine → N-{1-(R)-[4-(3,4-dichlorobenzyl)piperazin-1-ylmethyl]-2-methylpropyl}-4-fluorobenzenesulfonamide

https://huagongshe.com/reaction/1610901

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4-Fluorobenzenesulfonyl chlorideHCID 9588—
반응물n-{1(Rs)-[3-methyl-4-(3,4-dichlorobenzyl)piperazin-1-ylmethyl]-2-methylpropyl}-4-methylbenzamide dihydrochloride saltHCID 22257752—
용매DichloromethaneHCID 6344—
생성물N-{1-(R)-[4-(3,4-dichlorobenzyl)piperazin-1-ylmethyl]-2-methylpropyl}-4-fluorobenzenesulfonamideHCID 1834605966.9%

반응 단계

Triethylamine (21 ml, 0.15 mmol) and 4-fluorobenzenesulfonyl chloride (29 mg, 0.15 mmol) were added to a solution of 1-(R)-[4-(3,4-dichlorobenzyl)piperazin-1-ylmethyl]-2-methylpropylamine (50 mg, 0.15 mmol) [prepared as described in Example 1 above] in methylene chloride (1.5 ml). The reaction mixture was stirred for 2 h, then concentrated. Purification by flash chromatography with 20:1 methylene: methanol as the eluant gave N-{1-(R)-[4-(3,4-dichlorobenzyl)piperazin-1-ylmethyl]-2-methylpropyl}-4-fluorobenzenesulfonamide (49 mg) as a solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06984637B2
출처 데이터셋uspto-grants-2006_01
ORD IDord-9c9a483654944f90833d4880c6e68a69
출처 메모uspto-grants-2006_01