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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2111880생성일: 2026년 10월 26일

Water → 5-[4-(4-(2-(2-t-Butoxycarbonylaminopropanamido)-2-methoxycarbonylethyl)phenoxy)benzylidene]thiazolidin-2,4-dione

https://huagongshe.com/reaction/2111880

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물2-N-Boc-aminopropionic acidHCID 268471—
반응물5[4-(4-(2-Amino-2-methoxycarbonylethyl)phenoxy)benzylidene]thiazolidin-2,4-dione hydrochlorideHCID 73038788—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물5-[4-(4-(2-(2-t-Butoxycarbonylaminopropanamido)-2-methoxycarbonylethyl)phenoxy)benzylidene]thiazolidin-2,4-dioneHCID 8659744336.3%

반응 단계

A solution of 5-[4-(4-(2-amino-2-methoxycarbonylethyl)phenoxy)benzylidene]thiazolidin-2,4-dione hydrochloride (2 g, 4.6 mmol) and 2-t-butoxycarbonylamino propionic acid (0.87 g, 4.6 mmol) in dimethyl formamide (10 ml) was stirred for 1 h at 0° C. N,N′-Dicyclohexylcarbodiimide (1.139 g, 5.5 mmol) was added to this solution and stirring was continued for 2 h at ambient temperature. Water (200 ml) was added to the reaction mixture, stirred for 15 minutes, ethyl acetate (250 ml) added and stirring was continued for another 15 minutes. The organic layer was separated and washed with water (100 ml), dried over anhydrous sodium sulfate and concentrated to furnish the crude compound which was purified by column chromatography (0.95 g, yield 36.3%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07521466B2
출처 데이터셋uspto-grants-2009_04
ORD IDord-bd613d76a4c940b1939544a2a98c3e11
출처 메모uspto-grants-2009_04