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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 866452생성일: 2026년 10월 26일

Pyridine → HCID 178477371, 화합물

https://huagongshe.com/reaction/866452

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Phosphorus pentachlorideHCID 24819—
반응물alpha-t-Butyloxycarbonylamino-alpha-[2-(chloroacetamido)thiazol-4-yl)acetic acidHCID 12763201—
반응물HCID 178477368HCID 178477368—
용매DichloromethaneHCID 6344—
생성물HCID 178477371HCID 17847737162.2%

반응 단계

To a suspension of 349 mg of α-t-butyloxycarbonylamino-α-[2-(chloroacetamido)thiazol-4-yl)acetic acid in 5 ml of methylene chloride is added 249 mg of phosphorous pentachloride, and the mixture is stirred at room temperature. The mixture is added dropwise under stirring to the solution of 494 mg of 7β-amino-3-(1-methyl-1H-tetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid diphenylmethyl ester dissolved in 5 ml of methylene chloride, followed by the addition of 474 mg of pyridine. After that, the stirring is continued for further 1 hour at room temperature. The reaction solution is washed with 0.5N hydrochloric acid and then with water, and dried. The oily product obtained by the distillation of the solvent is purified by a column chromatography packed with silica gel. The procedure gives 513 mg of 7β-{α-t-butyloxycarbonylamino-α-[2-(chloroacetamido)thiazol-4-yl ]acetamido}-3-(1-methyl-1H-tetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid diphenylmethyl ester.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04098888
출처 데이터셋uspto-grants-1978_07
ORD IDord-6a3cf306c69d4bddb104dd7718daddfb
출처 메모uspto-grants-1978_07