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HRID 1477530作成日:2026年10月26日

(2-Oxopropyl)amine → (2S,4R)-4-tert-butoxy-2-(2-oxo-propylcarbamoyl)-pyrrolidine-1-carboxylic acid benzyl ester

https://huagongshe.com/reaction/1477530

反応式

関与物質

役割名称HCID仕込み量
反応物(2-Oxopropyl)amineHCID 215—
反応物TriethylamineHCID 8471—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物Z-Hyp(Tbu)-OHHCID 6950951—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物(2S,4R)-4-tert-butoxy-2-(2-oxo-propylcarbamoyl)-pyrrolidine-1-carboxylic acid benzyl esterHCID 8976839155.4%

反応手順

To a stirred solution of (2S,4R)-4-tert-butoxy-pyrrolidine-1,2-dicarboxylic acid 1-benzyl ester (10.78 g, 33.54 mmol) and 1-amino-propan-2-one (2.45 g, crude, 33.54 mmol) in dichlormethane (56 mL) were added EDC.HCl (6.405 g, 33.54 mmol), HOBt (5.128 g, 33.54 mmol) and triethylamine (12.67 mL, 100.62 mmol). The mixture was stirred at room temp. for 24 h. The reaction mixture was then diluted with water, extracted with dichloromethane and washed with water and brine. The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated. The crude was then purified by column chromatography to give (2S,4R)-4-tert-butoxy-2-(2-oxo-propylcarbamoyl)-pyrrolidine-1-carboxylic acid benzyl ester (7 g, 55.4% yield) as a light brown liquid. MS calcd. for C20H29N2O5 [(M+H)+] 377.0, obsd. 377.4.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09403805B2
出典データセットuspto-grants-2016_08
ORD IDord-f81b82f4fb1d4a5bb84bcff3f1415f2f
出典メモuspto-grants-2016_08