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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7349생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/7349

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물1-[(Tert-butoxy)carbonyl]pyrrolidine-2-carboxylic acidHCID 268472—
반응물5[4-(4-(2-Amino-2-methoxycarbonylethyl)phenoxy)benzylidene]thiazolidin-2,4-dione hydrochlorideHCID 73038788—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물2-(2-{4-[4-(2,4-dioxothiazolidin-5-ylidenemethyl)-phenoxy]-phenyl}-1-methoxycarbonylethylcarbamoyl)-pyrrolidine-1-carboxylic Acid Tert-Butyl EsterHCID 8659744132.4%

반응 단계

A solution of 5[4-(4-(2-amino-2-methoxycarbonylethyl)phenoxy)benzylidene]thiazolidin-2,4-dione hydrochloride (2.5 g, 5.76 mmol) and N-Boc-pyrolidin-2-carboxylic acid (1.238 g, 5.76 mmol) in dimethyl formamide (25 ml) was stirred for 60 minutes at 0° C. N,N′-Dicyclohexylcarbodiimide (1.423 g, 6.91 mmol) was added to it and stirring was continued for 10 h at ambient temperature. Water (200 ml) was added to the reaction mixture and stirred for 15 minutes. Ethyl acetate (200 ml) was added to the reaction mixture and stirring continued for another 15 minutes. The organic layer was separated, washed with water (75 ml), dried over anhydrous sodium sulphate and concentrated to afford the crude product, which was purified by column chromatography to furnish the required product (1.1 g, yield 32.4%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087576B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-63d709e139114d61af6aab85262e9c8f
출처 메모uspto-grants-2006_08