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HRID 343723作成日:2026年10月27日

m-Chloroperbenzoic acid → [1-[2-[3-(3,4-Dichlorophenyl)-1-(3,4,5-trimethoxybenzoyl)pyrrolidin-3-yl]ethyl]-4-phenylpiperidine-4-carbonyl]-oxidoazanium

https://huagongshe.com/reaction/343723

反応式

関与物質

役割名称HCID仕込み量
反応物m-Chloroperbenzoic acidHCID 70297—
反応物4-Phenyl-1-[2-[3-(3,4-dichlorophenyl)-1-(3,4,5-trimethoxybenzoyl)pyrrolidin-3-yl]ethyl]piperidine-4-carboxamideHCID 9874168—
溶媒DichloromethaneHCID 6344—
生成物[1-[2-[3-(3,4-Dichlorophenyl)-1-(3,4,5-trimethoxybenzoyl)pyrrolidin-3-yl]ethyl]-4-phenylpiperidine-4-carbonyl]-oxidoazaniumHCID 88374405—

反応条件

温度0 °C

反応手順

Combine 1-[2-[3-(3,4-dichloro-phenyl)-1-(3,4,5-trimethoxy-benzoyl)-pyrrolidin-3-yl]-ethyl]-4-phenyl-piperidine-4-carboxylic acid amide (1.0 mmol) and dichloromethane (10 mL). Cool to 0° C. Add portionwise, m-chloroperbenzoic acid (1.0 mmol). After the addition is complete, warm to ambient temperature. After 18 hours, extract the reaction mixture with water. Separate the organic layer, dry over MgSO4, filter, and evaporate in vacuo to give a residue. Purify the residue by chromatography to give the title compound.

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-e1aff303a3ab4e0885dfa3ea1b0a8c35
出典メモuspto-grants-1999_01