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HRID 1786560作成日:2026年10月26日

1,2-Dichloroethane → N-(1-Benzhydryl-2-oxo-pyrrolidin-3-yl)-2-diphenylamino-acetamide

https://huagongshe.com/reaction/1786560

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DichloroethaneHCID 11—
反応物(Diphenylamino)acetic acidHCID 735138—
反応物3-Amino-1-benzhydryl-pyrrolidin-2-oneHCID 57597562—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DichloromethaneHCID 6344—
生成物N-(1-Benzhydryl-2-oxo-pyrrolidin-3-yl)-2-diphenylamino-acetamideHCID 5759756769%

反応手順

To a solution of 3-amino-1-benzhydryl-pyrrolidin-2-one (42) (0.2 g, 0.75 mmol) in dry CH2Cl2 (20 ml)was added diphenylamino ethanoic acid (0.19 g, 0.82 mmol) under nitrogen. To the reaction was added EDC (0.18 g, 0.9 mmol) and DMAP (cat) and the reaction mixture was stirred under nitrogen at room temperature overnight. The reaction was then concentrated under reduced pressure. The residue was dissolved in ethyl acetate:water (10:1) (100 ml). The organic was washed with water (25 ml, 2×) and 10% NaOH (25 ml), dried over MgSO4 and evaporated to dryness. The resulting residue was purified by column chromatography using hexane:ethyl acetate (2:1) to give the desired product in 69% yield.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07507760B2
出典データセットuspto-grants-2009_03
ORD IDord-14563a3db8c14122aafee18220f7b5df
出典メモuspto-grants-2009_03