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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 543540생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/543540

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물DacthalHCID 2943—
반응물HCID 70463736HCID 70463736—
반응물HCID 178482017HCID 178482017—
용매AcetonitrileHCID 6342—
생성물7-Amino-3-(1-methyltetrazol-5-ylthiomethyl)-3-cephem-4-carboxylicacidHCID 1302081388%

반응 단계

A 4.0 ml portion of acetonitrile was added to 0.826 g of 7-amino-3-(3-carboxypropionyloxy)methyl-3-cephem-4-carboxylic acid and 0.32 g of 5-mercapto-1-methyl-1H-tetrazole, and 3.71 g of DCPA was added through a dropping funnel to the mixture under cooling at -5° to 0° C., followed by rinsing the funnel with 0.5 ml of acetonitrile. The mixture was stirred at the same temperature and turned into a solution. Then, the reaction solution was stirred for 45 minutes at 14° to 15° C. to allow the reaction to proceed. The reaction solution was cooled with ice, and poured into ice-water, which was placed in a refrigerator overnight and adjusted to pH 4.0 with 25% aqueous ammonia. The precipitated powder was recovered by filtration, washed with water and acetone successively, and dried, thereby affording 0.722 g (88.0% 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-38ad118902834c5099dd535d6bec4efd
출처 메모uspto-grants-1984_05