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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 979680생성일: 2026년 10월 24일

Thiourea → 7beta-[alpha-ethoxyimino-(2-aminothiazol-4-yl)acetamido]-3-(1-methyl-1H-tetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid benzhydryl ester

https://huagongshe.com/ko/reaction/979680

반응식

참여 물질

역할이름HCID투입량
반응물ThioureaHCID 2723790—
반응물7beta-{alpha-ethoxyimino-[2-(chloroacetamido)thiazol-4-yl]acetamido}-3-(1-methyl-1H-tetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid benzhydryl esterHCID 178474906—
촉매Benzyltriethylammonium bromideHCID 165294—
용매EthanolHCID 702—
용매TetrahydrofuranHCID 8028—
생성물7beta-[alpha-ethoxyimino-(2-aminothiazol-4-yl)acetamido]-3-(1-methyl-1H-tetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid benzhydryl esterHCID 17847490752.9%

반응 단계

To a solution of 2.2 g of 7β-{α-ethoxyimino-[2-(chloroacetamido)thiazol-4-yl]acetamido}-3-(1-methyl-1H-tetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid benzhydryl ester in 20 ml of tetrahydrofuran is added a solution of 550 mg of thiourea in 20 ml of ethanol, followed by addition of 50 mg of triethylbenzylammonium bromide. The mixture is stired for 20 hours at room temperature and concentrated. The residue is dissolved in a mixture of ethyl acetate and tetrahydrofuran and the solution was washed with aq. sodium bicarbonate solution and then water, followed by drying over anhydrous magnesium sulfate. The dried solution is subjected to distillation of the solvent to give powder which is washed with chloroform and ether and dried. The procedure yields 1.047 g of 7β-[α-ethoxyimino-(2-aminothiazol-4-yl)acetamido]-3-(1-methyl-1H-tetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid benzhydryl ester.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04668783
출처 데이터셋uspto-grants-1987_05
ORD IDord-18149d32e1094153be181bbf82fb7180
출처 메모uspto-grants-1987_05