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HRID 1080474作成日:2026年10月25日

Dicyclohexylcarbodiimide → Phenylmethyl-[2-[(3-benzoyl-1H-pyrrol-1-yl)amino]-2-oxoethyl]carbamate

https://huagongshe.com/reaction/1080474

反応式

関与物質

役割名称HCID仕込み量
反応物DicyclohexylcarbodiimideHCID 10868—
反応物BenzyloxycarbonylglycineHCID 14349—
反応物1-Amino-3-benzoylpyrroleHCID 19973156—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物Phenylmethyl-[2-[(3-benzoyl-1H-pyrrol-1-yl)amino]-2-oxoethyl]carbamateHCID 19973189—

反応手順

To a solution of (1-amino-1H-pyrrol-3-yl)phenylmethanone (5.96 g) and N-carbobenzyloxyglycine (6.69 g) in 70 ml of anhydrous DCM and 30 ml of anhydrous dimethylformamide was added DCC (7.22 g). The reaction mixture was stirred at room temperature for 4 hours and filtered. The filter cake was washed with ethyl acetate, and the combined filtrates were evaporated in vacuo. The residual oil was purified by preparative HPLC (silica gel, DCM/ethyl acetate 3:1). Evaporation of the desired fractions afforded a colorless oil, which was crystallized from DCM/ethyl ether yielding the product as colorless crystals (5.96 g), m.p. 144°-145° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05580987
出典データセットuspto-grants-1996_12
ORD IDord-84ee783b54b0491b93e4c26cb047146c
出典メモuspto-grants-1996_12