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HRID 543535作成日:2026年10月26日

Ammonia → 7-Amino-3-(2-ethoxycarbonylmethylthio-1,3,4-thiadiazol-5-yl)thiomethyl-3-cephem-4-carboxylic acid

https://huagongshe.com/reaction/543535

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物DacthalHCID 2943—
反応物7-Aminocephalosporanic acidHCID 441328—
反応物HCID 178473173HCID 178473173—
溶媒AcetonitrileHCID 6342—
生成物7-Amino-3-(2-ethoxycarbonylmethylthio-1,3,4-thiadiazol-5-yl)thiomethyl-3-cephem-4-carboxylic acidHCID 7046323792.8%

反応条件

温度40 °C

反応手順

A 8.0 ml portion of acetonitrile was added to 1.36 g of 7-ACA and 1.54 g of 2-ethoxycarbonylmethylthio-5-mercapto-1,3,4-thiadiazole, and the mixture was cooled to -40° to -30° C., followed by adding thereto dropwise 5.40 g of DCPA under stirring. The external bath was removed and the reaction mixture was stirred for 8 minutes, then warmed at 40° C. and stirred for 20 minutes to allow the reaction to proceed. The reaction solution was poured into 10 ml of ice-water, which was adjusted to pH 4.4 with 25% aqueous ammonia. The precipitated powder was recovered by filtration, washed with water and dried, thereby affording 2.08 g (92.7% of yield) of 7-amino-3-[(2-ethoxycarbonylmethylthio-1,3,4-thiadiazol-5-yl)thiomethyl]-3-cephem-4-carboxylic acid in the form of mud yellow powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04446318
出典データセットuspto-grants-1984_05
ORD IDord-b2f8e05831e84f959441fcce510434c4
出典メモuspto-grants-1984_05