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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2107174생성일: 2026년 10월 26일

Acetic Anhydride → 5-[1-(2-Acetylaminothiazol-4-yl)-1-ethoxycarbonylmethylene]-2,4-dioxothiazolidine-3-acetic acid

https://huagongshe.com/reaction/2107174

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AnhydrideHCID 7918—
반응물PiperidineHCID 8082—
반응물(2,4-Dioxo-1,3-thiazolidin-3-yl)acetic acidHCID 2770836—
반응물Ethyl 2-(3-phenylureido)thiazol-4-ylglyoxylateHCID 15053489—
반응물5-{1-Ethoxycarbonyl-1-hydroxy-1-[2-(3-phenylureido)thiazol-4-yl]methyl}-2,4-dioxothiazolidine-3-acetic acidHCID 23047573—
용매EthanolHCID 702—
용매WaterHCID 962—
용매PyridineHCID 1049—
생성물5-[1-(2-Acetylaminothiazol-4-yl)-1-ethoxycarbonylmethylene]-2,4-dioxothiazolidine-3-acetic acidHCID 53916800—

반응 조건

온도60 °C

반응 단계

A mixture comprising 0.6 g of crude 5-{1-ethoxycarbonyl-1-hydroxy-1-[2-(3-phenylureido)thiazol-4-yl]methyl}-2,4-dioxothiazolidine-3-acetic acid [prepared from 2.6 g of ethyl 2-(3-phenylureido)thiazol-4-ylglyoxylate, 1.2 g of 2,4-dioxothiazolidine-3-acetic acid, 1.2 g of piperidine and 30 ml of ethanol by a procedure similar to that of Example 24], 0.5 g of acetic anhydride and 4 ml of pyridine was heated at 60° C. for 17 hours. The reaction mixture was poured into water and extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate, and the solvent was evaporated off under reduced pressure. The resulting oil was purified by silica gel column chromatography, using as eluent a 8:2:0.5 to 7:3:0.5 by volume mixture of benzene ethyl acetate and acetic acid, giving the desired compound as a yellow powder having the following physical properties.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04933355
출처 데이터셋uspto-grants-1990_06
ORD IDord-77291116254c4c11b1dc110fd7121297
출처 메모uspto-grants-1990_06