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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Anhydride | HCID 7918 | — |
| 반응물 | Piperidine | HCID 8082 | — |
| 반응물 | (2,4-Dioxo-1,3-thiazolidin-3-yl)acetic acid | HCID 2770836 | — |
| 반응물 | Ethyl 2-(3-phenylureido)thiazol-4-ylglyoxylate | HCID 15053489 | — |
| 반응물 | 5-{1-Ethoxycarbonyl-1-hydroxy-1-[2-(3-phenylureido)thiazol-4-yl]methyl}-2,4-dioxothiazolidine-3-acetic acid | HCID 23047573 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 생성물 | 5-[1-(2-Acetylaminothiazol-4-yl)-1-ethoxycarbonylmethylene]-2,4-dioxothiazolidine-3-acetic acid | HCID 53916800 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04933355 |
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| 출처 데이터셋 | uspto-grants-1990_06 |
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| ORD ID | ord-77291116254c4c11b1dc110fd7121297 |
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| 출처 메모 | uspto-grants-1990_06 |
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