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HRID 7350作成日:2026年10月24日

Water → 2-(2-{4-[4-(2,4-dioxothiazolidin-5-ylmethyl)-phenoxy]-phenyl}-1-methoxycarbonylethylcarbamoyl)-pyrrolidine-1-carboxylic Acid Tert-Butyl Ester

https://huagongshe.com/ja/reaction/7350

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物DicyclohexylcarbodiimideHCID 10868—
反応物1-[(Tert-butoxy)carbonyl]pyrrolidine-2-carboxylic acidHCID 268472—
反応物2-Amino-3-[4-[4-[(2,4-dioxo-5-thiazolidinyl)methyl]phenoxy]phenyl]propanoic acid methyl ester hydrochlorideHCID 21989681—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物2-(2-{4-[4-(2,4-dioxothiazolidin-5-ylmethyl)-phenoxy]-phenyl}-1-methoxycarbonylethylcarbamoyl)-pyrrolidine-1-carboxylic Acid Tert-Butyl EsterHCID 8659744251.2%

反応手順

A solution of 5-[4-(4-(2-amino-2-methoxycarbonylethyl)phenoxy)benzyl]thiazolidin-2,4-dione hydrochloride (2.03 g, 4.65 mmol) and N-t-butoxycarbonylpyrrolidin-2-carboxylic acid (1 g, 4.65 mmol) in N,N-dimethylformamide (20 ml) was stirred for 1 h at 0° C. N,N′-Dicyclohexylcarbodiimide (0.96 g, 4.65 mmol) was added to this solution and stirring was continued for 2 h at ambient temperature. Water (150 ml) was added to the reaction mixture, stirred for 20 minutes, ethyl acetate (200 ml) was added and stirring continued for another 15 minutes. The organic layer was separated and washed with water (100 ml), dried over anhydrous sodium sulfate and concentrated to give the crude compound, which was purified by column chromatography (1.42 g, yield 51.2%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087576B2
出典データセットuspto-grants-2006_08
ORD IDord-964f5c140dda483dbe6b8a944fee6afc
出典メモuspto-grants-2006_08