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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 543539생성일: 2026년 10월 25일

Dacthal → 7-Amino-3-(1-methyltetrazol-5-ylthiomethyl)-3-cephem-4-carboxylicacid

https://huagongshe.com/reaction/543539

반응식

참여 물질

역할이름HCID투입량
반응물DacthalHCID 2943—
반응물HCID 70463326HCID 70463326—
반응물HCID 178482017HCID 178482017—
용매AcetonitrileHCID 6342—
생성물7-Amino-3-(1-methyltetrazol-5-ylthiomethyl)-3-cephem-4-carboxylicacidHCID 1302081386.5%

반응 조건

온도0 °C

반응 단계

A 3.5 ml portion of acetonitrile was added to 0.946 g of 7-amino-3-(2-carboxybenzoyloxy)methyl-3-cephem-4-carboxylic acid and 0.32 g of 5-mercapto-1-methyl-1H-tetrazole, and the mixture was cooled over a dry-ice/ethanol bath, followed by adding through a dropping funnel 3.71 g of DCPA to it with stirring and rinsing the funnel with 1.0 ml of acetonitrile. The external bath was removed, and the reaction mixture was warmed to 0° C., whereby the starting materials dissolved. The solution was stirred at 14° to 16° C. for 40 minutes to allow the reaction to proceed, and the reaction solution was cooled with ice, and poured into ice-water, which was placed in a refrigerator overnight. The precipitate was filtered out and washed with 10 ml of water, and the filtrate and washing were combined and adjusted to pH 4.0 with 25% aqueous ammonia under ice cooling. The precipitated powder was recovered by filtration, washed with water and acetone successively, and dried, thereby affording 0.710 g (86.5% of yield) of 7-amino-3-(1-methyl-1H-tetrazol-5-yl)thiomethyl-3-cephem-4-carboxylic acid. The IR and NMR values of the product were in accordance with those of the authentic sample.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04446318
출처 데이터셋uspto-grants-1984_05
ORD IDord-85c49044718c4f0c915c14e5dbcdb505
출처 메모uspto-grants-1984_05