戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 543542作成日:2026年10月27日

Ammonia → 7-Amino-3-(1-methyltetrazol-5-ylthiomethyl)-3-cephem-4-carboxylicacid

https://huagongshe.com/reaction/543542

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物7-Aminocephalosporanic acidHCID 441328—
反応物Diphosphoryl tetrachlorideHCID 4432411—
反応物HCID 178482017HCID 178482017—
溶媒WaterHCID 962—
溶媒AcetonitrileHCID 6342—
生成物7-Amino-3-(1-methyltetrazol-5-ylthiomethyl)-3-cephem-4-carboxylicacidHCID 1302081387.2%

反応条件

温度-40 °C

反応手順

In 5.4 ml of acetonitrile were suspended 0.909 g of 7-ACA and 0.504 g of 5-mercapto-1-methyl-1H-tetrazole, and 0.256 g of water was added. The suspension was cooled at -40° C. under stirring, and 3.58 g of diphosphoryl tetrachloride was added dropwise to it at -50° to -35° C. The reaction mixture was stirred at -35° to 0° C. for 5 minutes after the dropwise addition and placed in a warm water bath at 40° C. to warm, followed by stirring at the same temperature for 20 minutes. The reaction solution was cooled over an ice water bath and, after the addition of 11 ml of cold water, it was adjusted to pH 4.0 with aqueous concentrated ammonia. The separated-out precipitate was recovered by filtration, washed with water and dried, thereby affording 0.956 g of 7-amino-3-(1-methyl-1H-tetrazol-5-yl)thiomethyl-3-cephem-4 -carboxylic acid. The yield was 87.2%.

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-0c37b6a37da346a8af4bc11f1565cc12
出典メモuspto-grants-1984_05