関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Chlorotrimethylsilane | HCID 6397 | — |
| 反応物 | Phenylacetyl chloride | HCID 7679 | — |
| 反応物 | Cephalothin Sodium | HCID 23675321 | — |
| 反応物 | Monosilyltrifluoroacetamide | HCID 123231972 | — |
| 生成物 | 7-(Phenylacetyl-2-thienylacetyl)amino-3-acetoxymethyl-3-cephem-4-carboxylic acid | HCID 88743706 | — |
反応手順
A suspension of sodium cephalothin (3.36 g.) in anhydrous alcohol-free chloroform (20 ml.) is silylated by the addition of trimethylchlorosilane (2.2 ml.). After stirring for 30 minutes, monosilyltrifluoroacetamide (5.0 ml.) and phenylacetyl chloride (4.0 ml.) are added and the mixture is then heated to 45° C. for two days under a condenser fitted with a drying tube. The volatiles are evaporated to afford a residue which is dissolved in 100 ml. of ethyl acetate and washed three times with water. The ethyl acetate layer is dried over magnesium sulfate, filtered and the solution evaporated in vacuo to a residue. The residue is triturated with chloroform, any insolubles are removed by filtration and the product precipitated from the filtrate with hexane. This procedure is followed two more times. The 7-(phenylacetyl-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 | US04342757 |
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| 出典データセット | uspto-grants-1982_08 |
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| ORD ID | ord-6ec1b66b982943509e0e77e0253e85ba |
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| 出典メモ | uspto-grants-1982_08 |
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