戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 894834作成日:2026年10月25日

Phosphorisocyanatidic dichloride → Cefuroxime

https://huagongshe.com/reaction/894834

反応式

関与物質

役割名称HCID仕込み量
反応物Phosphorisocyanatidic dichlorideHCID 70090—
反応物Sodium AcetateHCID 517045—
反応物(6R,7R)-7-(((2Z)-2-(2-Furanyl)-2-(methoxyimino)acetyl)amino)-3-(hydroxymethyl)-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acidHCID 9800056—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物CefuroximeHCID 5479529—

反応手順

Dichlorophosphinyl isocyanate (1.46 ml,) was added to a solution of (6R,7R)-7-[Z-2-(fur-2-yl)-2-methoxyiminoacetamido]-3-hydroxymethylceph-3-em-4-carboxylic acid (3.81 g) in THF (50 ml) at 22°, the temperature rising to 31°. The reaction mixture was stirred for 15 minutes and then added to a solution of sodium acetate (5.72 g) in water (50 ml). More sodium acetate (1.64 g) was added over 10 minutes to give a stable pH of 4.6. This solution was stirred at 30° for 1 hour and then heated at 45° for 3.5 hours when TLC (as Example 3) showed the reaction to be complete. The solution, pH 4.6, was clarified by filtration, adjusted to pH 7.0 with aqueous NaHCO3 solution and washed twice with ethyl acetate. The aqueous phase was stirred and acidified to pH 1.9 with dilute hydrochloric acid to precipitate the title compound (2.80 g, 66.0%); purity by HPLC 95.8% and by TLC 96%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04284767
出典データセットuspto-grants-1981_08
ORD IDord-b7a20f3b370d49f79a0e20fdd05b1b08
出典メモuspto-grants-1981_08