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HRID 894826作成日:2026年10月26日

(6R,7R)-7-[[(2Z)-2-(furan-2-yl)-2-methoxyiminoacetyl]amino]-8-oxo-3-(phosphonocarbamoyloxymethyl)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid → Cefuroxime

https://huagongshe.com/reaction/894826

反応式

関与物質

役割名称HCID仕込み量
反応物(6R,7R)-7-[[(2Z)-2-(furan-2-yl)-2-methoxyiminoacetyl]amino]-8-oxo-3-(phosphonocarbamoyloxymethyl)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acidHCID 88760882—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物CefuroximeHCID 5479529—

反応手順

A solution of (6R,7R)-3-phosphonocarbamoyloxymethyl-7-[Z-2-(fur-2-yl)-2-methoxyiminoacetamido]ceph-3-em-4-carboxylic acid (0.35 g) in water (4 ml) and dioxan (1 ml) was kept successively at 40° for 5 hours, room temperature for 16 hours, 40° for 6 hours and 20° for 16 hours. The conversion to the title compound was monitored by t.l.c. A precipitate was formed and this was filtered off. The pH was altered from 4 to 7 by addition of saturated aqueous sodium bicarbonate solution.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04284766
出典データセットuspto-grants-1981_08
ORD IDord-bd40260fbe4b4d48b95539e02487ee8f
出典メモuspto-grants-1981_08