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HRID 66643作成日:2026年10月24日

Chlorotrimethylsilane → 7-(Phenylacetyl-2-thienylacetyl)amino-3-acetoxymethyl-3-cephem-4-carboxylic acid

https://huagongshe.com/ja/reaction/66643

反応式

関与物質

役割名称HCID仕込み量
反応物ChlorotrimethylsilaneHCID 6397—
反応物Phenylacetyl chlorideHCID 7679—
反応物Cephalothin SodiumHCID 23675321—
反応物MonosilyltrifluoroacetamideHCID 123231972—
生成物7-(Phenylacetyl-2-thienylacetyl)amino-3-acetoxymethyl-3-cephem-4-carboxylic acidHCID 88743706—

反応条件

温度45 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04342757
出典データセットuspto-grants-1982_08
ORD IDord-6ec1b66b982943509e0e77e0253e85ba
出典メモuspto-grants-1982_08