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HRID 59788作成日:2026年10月26日

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

https://huagongshe.com/reaction/59788

反応式

関与物質

役割名称HCID仕込み量
反応物PhenylsilaneHCID 12752—
反応物Allyl 4-((2-benzamidoethyl)(4-chlorophenethyl)amino)piperidine-1-carboxylateHCID 121410296—
溶媒DichloromethaneHCID 6344—
生成物N-(2-((4-chlorophenethyl)(piperidin-4-yl)amino)ethyl)benzamideHCID 121410331—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09440953B2
出典データセットuspto-grants-2016_09
ORD IDord-15eac85c8f2845f999467b18e820542b
出典メモuspto-grants-2016_09