関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Chlorotrimethylsilane | HCID 6397 | — |
| 反応物 | 2-Thiopheneacetyl chloride | HCID 162362 | — |
| 反応物 | Cephalothin Sodium | HCID 23675321 | — |
| 反応物 | Monosilyltrifluoroacetamide | HCID 123231972 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | 7-(Di-2-thienylacetyl)amino-3-acetoxymethyl-3-cephem-4-carboxylic acid | HCID 70541217 | — |
反応手順
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 obtain 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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04342869 |
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| 出典データセット | uspto-grants-1982_08 |
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| ORD ID | ord-5ff319df6c5b47bba3a595b68dcf6c08 |
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| 出典メモ | uspto-grants-1982_08 |
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