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HRID 343656作成日:2026年10月25日

4-Phenylpiperidine-4-carboxamide monohydrochloride → 1-[2-[3-(3,4-Dimethoxy-phenyl)-1-(3,4,5-trimethoxy-benzoyl)-pyrrolidin-3-yl]-ethyl]-4-phenyl-piperidine-4-carboxylic acid amide

https://huagongshe.com/reaction/343656

反応式

関与物質

役割名称HCID仕込み量
反応物4-Phenylpiperidine-4-carboxamide monohydrochlorideHCID 3017129—
反応物2-[3-(3,4-Dimethoxy-phenyl)-1-(3,4,5-trimethoxy-benzoyl)-pyrrolidin-3-yl]-ethyl-methanesulfonateHCID 86750910—
生成物1-[2-[3-(3,4-Dimethoxy-phenyl)-1-(3,4,5-trimethoxy-benzoyl)-pyrrolidin-3-yl]-ethyl]-4-phenyl-piperidine-4-carboxylic acid amideHCID 44319249—

反応手順

Prepared by the method of example 3.3 using 2-[3-(3,4-dimethoxy-phenyl)-1-(3,4,5-trimethoxy-benzoyl)-pyrrolidin-3-yl]-ethyl-methanesulfonate (0.55 mmol) and 4-phenyl-piperidine-4-carboxylic acid amide hydrochloride (175 mg, 0.73 mmol). Chromatography on silica gel (30 g) eluting sequentially with ethyl acetate, 6% methanol in dichloromethane, and 10% methanol in dichloromethane gave the title compound: Rf =0.39 (silica gel, 10% methanol in dichloromethane).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05861416
出典データセットuspto-grants-1999_01
ORD IDord-3e85ddd2db3b44f8beb70f70ec4fb739
出典メモuspto-grants-1999_01