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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 59788생성일: 2026년 10월 26일

Phenylsilane → N-(2-((4-chlorophenethyl)(piperidin-4-yl)amino)ethyl)benzamide

https://huagongshe.com/reaction/59788

반응식

참여 물질

역할이름HCID투입량
반응물PhenylsilaneHCID 12752—
반응물Allyl 4-((2-benzamidoethyl)(4-chlorophenethyl)amino)piperidine-1-carboxylateHCID 121410296—
용매DichloromethaneHCID 6344—
생성물N-(2-((4-chlorophenethyl)(piperidin-4-yl)amino)ethyl)benzamideHCID 121410331—

반응 단계

The solution of allyl 4-((2-benzamidoethyl)(4-chlorophenethyl)amino)piperidine-1-carboxylate, PhSiH3 (5 equiv) in DCM (8 mL/mmol) was degassed for 10 min by bubbling argon through the inserted needle, prior to the addition of Pd(Ph3P)4 (5 mol %). After 20 min TLC indicated completion of reaction. The reaction was concentrated and was purified by column chromatography in DCM/MeOH solvent system (gradient 100:1 to 10:1) to give pure product in a form of an off-white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09440953B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-15eac85c8f2845f999467b18e820542b
출처 메모uspto-grants-2016_09