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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2213706생성일: 2026년 10월 26일

Sulfuric Acid → Cefdinir

https://huagongshe.com/reaction/2213706

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물TetrahydrofuranHCID 8028—
반응물7-Amino-3vinyl-3-cephem-4-carboxylic acidHCID 12818006—
반응물HCID 178476694HCID 178476694—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
용매TriethylamineHCID 8471—
생성물CefdinirHCID 691594462.9%

반응 단계

40 g of 7-amino-3-vinyl-3-cephem-4-carboxylic acid (AVNA, 0.177 mol) was added to 400 ml of tetrahydrofuran under nitrogen atmosphere followed by 78 g of O-acetyl thioester (0.206 mol, prepared in Example 1) and 200 ml of water with stirring. Cooled the reaction mass to 15–20° C. To this reaction mixture, 20 g of triethylamine was added slowly at pH ˜8.5. Stirring was continued and progress of the reaction was monitored by qualitative HPLC till AVNA was less than 1%. At this stage 400 ml of methylene dichloride was added and stirred for further 15 min at 20–25° C. 200 ml of water was added and stirred the reaction mass for 15 min at 20–25° C. Separated the layers and to the aqueous layer, 20% w/v aqueous potassium carbonate solution was added and maintained pH at 8.1–8.2 at 20–25° C. Thereafter, 26.4 g of ammonium chloride was added in one lot at 20–25° C. and continued maintaining the pH between 8.0 to 8.2 by addition of 20% w/v aqueous potassium carbonate solution. The progress of reaction was monitored by qualitative HPLC till O-acetyl cefdinir is less than 0.5%. Adjusted the pH of reaction mass to 2.4–2.5 with conc. sulfuric acid maintaining temperature between 35° to 40° C. The precipitated product was filtered and dried at 40–45° C. under reduced pressure till moisture content was ≦2% wiw. 44 g of product was obtained in 99.3% purity (by HPLC).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07105659B2
출처 데이터셋uspto-grants-2006_09
ORD IDord-ec1b8ddfb5a343738a259eb80bb9de58
출처 메모uspto-grants-2006_09