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HRID 31377作成日:2026年10月24日

Tranylcypromine → 4-(2-Phenyl-cyclopropylcarbamoyl)-pyrrolidine-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester

https://huagongshe.com/ja/reaction/31377

反応式

関与物質

役割名称HCID仕込み量
反応物TranylcypromineHCID 5530—
反応物DicyclohexylcarbodiimideHCID 10868—
反応物N-HydroxysuccinimideHCID 80170—
反応物(3S,5S)-1-benzyloxycarbonyl-5-methoxycarbonyl-pyrrolidine-3-carboxylic acidHCID 69197850—
溶媒DichloromethaneHCID 6344—
溶媒1,4-DioxaneHCID 31275—
生成物4-(2-Phenyl-cyclopropylcarbamoyl)-pyrrolidine-1,2-dicarboxylic acid 1-benzyl ester 2-methyl esterHCID 6919738775%

反応手順

To a stirred solution of cis-N-(benzyloxycarbonyl)-4-carboxy-proline methyl ester (615 mg, 2 mmol) and HOSu (173 mg, 3 mmol) in 1,4-dioxane (2 mL) was added a solution of DCC (454 mg, 2.2 mmol) in CH2Cl2 (2 mL). After 10 min at room temperature, 2-phenylcyclopropylamine (266 mg, 2 mmol) in CH2Cl2 (1 mL) was added with stirring. After 16 h, the resulting N,N′-dicyclohexylurea was removed by filtration. The filtrate was washed with saturated aqueous NaHCO3 (5 mL), 1 N aqueous citric acid (5 mL), water (5 mL), dried over MgSO4 and concentrated. The residue was purified by a silica gel column using hexane/EtOAc (6:4) as eluant to yield the desired compound as a colorless oil (633 mg, 75%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07425633B2
出典データセットuspto-grants-2008_09
ORD IDord-26527388890d4e089a4090d1d975f81f
出典メモuspto-grants-2008_09