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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 26040생성일: 2026년 10월 24일

Acetone → 7-(2-thienylacetamido)-3-(1-methyl-1H-tetrazol-5-yl)vinyl-3-cephem-4-carboxylic acid

https://huagongshe.com/ko/reaction/26040

반응식

참여 물질

역할이름HCID투입량
반응물AcetoneHCID 180—
반응물2-Thiopheneacetyl chlorideHCID 162362—
반응물Sodium BicarbonateHCID 516892—
반응물7-amino-3-(1-methyl-1H-tetrazol-5-yl)vinyl-3-cephem-4-carboxylic acidHCID 131711472—
용매WaterHCID 962—
생성물7-(2-thienylacetamido)-3-(1-methyl-1H-tetrazol-5-yl)vinyl-3-cephem-4-carboxylic acidHCID 131711471101.1%

반응 단계

In 40 ml of water were dissolved 416 mg of 7-amino-3-(1-methyl-1H-tetrazol-5-yl)vinyl-3-cephem-4-carboxylic acid and 660 mg of sodium hydrogencarbonate. To the solution was added 10 ml of acetone and further added dropwise with stirring at 0°-5° C., 20 ml of an acetone solution containing 323 mg of 2-thienylacetyl chloride. The mixture was stirred for 30 minutes under ice-cooling and for additional 3 hours at room temperature. The acetone was distilled off at room temperature under reduced pressure. The residual solution was washed with ether, adjusted to pH 2.0 with 10% hydrochloric acid and extracted with ethyl acetate. The extract was washed with an aqueous sodium chloride solution and dried over anhydrous sodium sulfate. The ethyl acetate was removed under reduced pressure, and, upon washing the residue with ether, there was obtained 590 mg of 7-(2-thienylacetamido)-3-(1-methyl-1H-tetrazol-5-yl)vinyl-3-cephem-4-carboxylic acid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04147863
출처 데이터셋uspto-grants-1979_04
ORD IDord-29b0d6884b9a4451b5e5cdca3673477c
출처 메모uspto-grants-1979_04