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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Water | HCID 962 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 1(3H)-Isobenzofuranone, 3-bromo- | HCID 96218 | — |
| 반응물 | 7beta-[2-(2-Amino-5-chloro-4-thiazolyl)-2-methoxyiminoacetamido]-3-cephem-4-carboxylic acid | HCID 131712102 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 7beta-[2-(2-Amino-5-chloro-4-thiazolyl)-2-methoxyiminoacetamido]-3-cephem-4-carboxylic acid phthalidyl ester | HCID 131712108 | 80% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04254119 |
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| 출처 데이터셋 | uspto-grants-1981_03 |
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| ORD ID | ord-4e3ef60a8e184445b7789b10ae164850 |
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| 출처 메모 | uspto-grants-1981_03 |
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