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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7350생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물1-[(Tert-butoxy)carbonyl]pyrrolidine-2-carboxylic acidHCID 268472—
반응물2-Amino-3-[4-[4-[(2,4-dioxo-5-thiazolidinyl)methyl]phenoxy]phenyl]propanoic acid methyl ester hydrochlorideHCID 21989681—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물2-(2-{4-[4-(2,4-dioxothiazolidin-5-ylmethyl)-phenoxy]-phenyl}-1-methoxycarbonylethylcarbamoyl)-pyrrolidine-1-carboxylic Acid Tert-Butyl EsterHCID 8659744251.2%

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087576B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-964f5c140dda483dbe6b8a944fee6afc
출처 메모uspto-grants-2006_08