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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 126905생성일: 2026년 10월 26일

Water → 7beta-[2-(2-Amino-5-chloro-4-thiazolyl)-2-methoxyiminoacetamido]-3-cephem-4-carboxylic acid phthalidyl ester

https://huagongshe.com/reaction/126905

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물TriethylamineHCID 8471—
반응물1(3H)-Isobenzofuranone, 3-bromo-HCID 96218—
반응물7beta-[2-(2-Amino-5-chloro-4-thiazolyl)-2-methoxyiminoacetamido]-3-cephem-4-carboxylic acidHCID 131712102—
용매DimethylformamideHCID 6228—
생성물7beta-[2-(2-Amino-5-chloro-4-thiazolyl)-2-methoxyiminoacetamido]-3-cephem-4-carboxylic acid phthalidyl esterHCID 13171210880%

반응 단계

To a solution of 7β-[2-(2-amino-5-chloro-4-thiazolyl)-2-methoxyiminoacetamido]-3-cephem-4-carboxylic acid (209 mg) in N,N-dimethylformamide (5 ml) are added triethylamine (0.07 ml) and phthalidyl bromide (128 mg), and the mixture is stirred at room temperature for 20 minutes. The reaction mixture is poured into water and the separated precipitate is collected by filtration. The solid material is dissolved in ethyl acetate, washed with water, diluted aqueous sodium hydrogen carbonate solution, water, diluted aqueous phosphoric acid and water, dried, and evaporated. Purification of the residue by silica gel column chromatography gives 7β-[2-(2-amino-5-chloro-4-thiazolyl)-2-methoxyiminoacetamido]-3-cephem-4-carboxylic acid phthalidyl ester (220 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04254119
출처 데이터셋uspto-grants-1981_03
ORD IDord-4e3ef60a8e184445b7789b10ae164850
출처 메모uspto-grants-1981_03