Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 66644생성일: 2026년 10월 25일
Chlorotrimethylsilane → 7-(Di-2-thienylacetyl)amino-3-acetoxymethyl-3-cephem-4-carboxylic acid
https://huagongshe.com/reaction/66644
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Chlorotrimethylsilane | HCID 6397 | — |
| 반응물 | 2-Thiopheneacetyl chloride | HCID 162362 | — |
| 반응물 | Cephalothin Sodium | HCID 23675321 | — |
| 반응물 | Monosilyltrifluoroacetamide | HCID 123231972 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | 7-(Di-2-thienylacetyl)amino-3-acetoxymethyl-3-cephem-4-carboxylic acid | HCID 70541217 | — |
반응 단계
A suspension of sodium cephalothin (1.18 g.) in anhydrous alcohol-free chloroform (10 ml.) is silylated by the addition of trimethylchlorosilane (1.1 ml.). After stirring for 30 minutes, monosilyltrifluoroacetamide (2.5 ml.) and 2-thienylacetyl chloride (2.0 ml.) are added to the suspension which is then heated to 45° C. The mixture is allowed to remain at this temperature for two days and then evaporated in vacuo to a residue which is dissolved in ethyl acetate (50 ml.) and washed three times with water. The ethyl acetate layer is dried over magnesium sulfate, filtered and the filtrate evaporated in vacuo to obtained a residue. The residue is dissolved in chloroform and precipitated with hexane three times, each time discarding the supernatent liquid. The 7-(di-2-thienylacetyl)amino-3-acetoxymethyl-3-cephem-4-carboxylic acid is obtained in a solvent-free form by freeze-drying from a solution in benzene.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04342757 |
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| 출처 데이터셋 | uspto-grants-1982_08 |
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| ORD ID | ord-5bd39d5c12d448c8a6d7ff4fbd656c60 |
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| 출처 메모 | uspto-grants-1982_08 |
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