戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 261976作成日:2026年10月25日

Acetic Acid → 3-Acetoxymethyl-7-[2-(2-tritylamino-4-thiazolyl)-2-methoxyiminoacetamido]-3-cephem-4-carboxylic acid

https://huagongshe.com/reaction/261976

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物DicyclohexylcarbodiimideHCID 10868—
反応物7-Aminocephalosporanic acidHCID 441328—
反応物(Z)-2-(2-Tritylaminothiazol-4-yl)-2-methoxyiminoacetic acidHCID 2724510—
溶媒DichloromethaneHCID 6344—
溶媒TriethylamineHCID 8471—
溶媒Ethyl AcetateHCID 8857—
生成物3-Acetoxymethyl-7-[2-(2-tritylamino-4-thiazolyl)-2-methoxyiminoacetamido]-3-cephem-4-carboxylic acidHCID 131711502—

反応手順

0.78 g of dicyclohexylcarbodiimide was added to a solution of the dry acid of Step C in 30 ml of dry methylene chloride and the mixture was stirred for an hour at room temperature and ws then vacuum filtered to remove dicyclohexyl urea formed. The filtrate was cooled to -10° C. and a solution of 1.01 g of 7-amino-cephalosporanic acid in 13 ml of methylene chloride and 0.9 ml of triethylamine was added. The temperature returned to room temperature and 1 ml of acetic acid was added thereto. The mixture was vacuum filtered and the filtrate was washed with aqueous hydrochloric acid, dried and concentrated to dryness. The residue was taken up in 10 ml of dioxane and 1 ml of water and 3 ml of a saturated sodium bicarbonate aqueous solution were added thereto. The mixture was stirred and vacuum filtered and the filtrate was washed and evaporated to dryness. The residue was taken up in methylene chloride and the solution was washed with 10 ml of water and 5 ml of N hydrochloric acid. The mixture was decanted and the organic phase was washed with water, dried and effloresced with ether to obtain 1.747 g of raw product. The latter was dissolved in ethyl acetate and was crystallized by addition of ether to obtain 1.255 g of pure 3-acetoxymethyl-7-[2-(2-tritylamino-4-thiazolyl)-2-methoxyiminoacetamido]-ceph-3-eme-4-carboxylic acid in the syn configuration.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04152432
出典データセットuspto-grants-1979_05
ORD IDord-8ca57078ca924c93b87422347ab1d997
出典メモuspto-grants-1979_05