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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1656263생성일: 2026년 10월 25일

Phosphorus oxychloride → HCID 131714064, 화합물

https://huagongshe.com/reaction/1656263

반응식

참여 물질

역할이름HCID투입량
반응물Phosphorus oxychlorideHCID 24813—
반응물Acetamide, 2-(trimethylsilyl)-HCID 357676—
반응물7-Amino-3vinyl-3-cephem-4-carboxylic acidHCID 12818006—
반응물2-(p-Nitrobenzyloxycarbonylmethoxyimino)-2-(2-formamidothiazol-4-yl)acetic acidHCID 54535272—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물HCID 131714064HCID 13171406473.4%

반응 단계

Vilsmeir reagent was prepared from N,N-dimethylformamide (1.67 ml) and phosphorus oxychloride (1.98 ml) in dry tetrahydrofuran (50.4 ml) in a conventional manner. 2-(p-Nitrobenzyloxycarbonylmethoxyimino)-2-(2-formamidothiazol-4-yl)acetic acid (syn isomer) (7.35 g) was added to the stirred suspension of Vilsmeir reagent under ice-cooling, followed by stirring for 30 minutes at the same temperature. To a solution of 7-amino-3-vinyl-3-cephem-4-carboxylic acid (3.4 g) and trimethylsilylacetamide (11.8 g) in ethyl acetate (35 ml) was added the activated acid solution obtained above at -20° C., and the reaction mixture was stirred at -20° C. to -10° C. for an hour. After water and ethyl acetate were added to the resultant solution, the separated organic layer was washed with water and then dried. A conventional work-up of the solution gave 7-[2-(p-nitrobenzyloxycarbonylmethoxyimino)-2-(2-formamidothiazol-4-yl)acetamido]-3-vinyl-3-cephem-4-carboxylic acid (syn isomer) (6.8 g) as yellowish powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05252731
출처 데이터셋uspto-grants-1993_10
ORD IDord-8c26705f6be24634ae3b0cca9ed0e382
출처 메모uspto-grants-1993_10