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HRID 66644作成日:2026年10月26日

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

https://huagongshe.com/reaction/66644

反応式

関与物質

役割名称HCID仕込み量
反応物ChlorotrimethylsilaneHCID 6397—
反応物2-Thiopheneacetyl chlorideHCID 162362—
反応物Cephalothin SodiumHCID 23675321—
反応物MonosilyltrifluoroacetamideHCID 123231972—
溶媒ChloroformHCID 6212—
生成物7-(Di-2-thienylacetyl)amino-3-acetoxymethyl-3-cephem-4-carboxylic acidHCID 70541217—

反応条件

温度45 °C

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 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.

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-5bd39d5c12d448c8a6d7ff4fbd656c60
出典メモuspto-grants-1982_08