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HRID 543530作成日:2026年10月25日

Potassium → 3-methylbutanoyloxymethyl (6R,7R)-3-(carbamoyloxymethyl)-7-[[(2Z)-2-(furan-2-yl)-2-methoxyiminoacetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

https://huagongshe.com/reaction/543530

反応式

関与物質

役割名称HCID仕込み量
反応物PotassiumHCID 5462222—
反応物CefuroximeHCID 5479529—
反応物Bromomethyl 3-methylbutanoateHCID 20461839—
溶媒DimethylformamideHCID 6228—
生成物3-methylbutanoyloxymethyl (6R,7R)-3-(carbamoyloxymethyl)-7-[[(2Z)-2-(furan-2-yl)-2-methoxyiminoacetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylateHCID 177714162—

反応手順

Bromomethyl 3-methylbutanoate (1.328 g, 6.7 mmole) was added to a solution of (6R,7R)-3-carbamoyloxymethyl-7-[(Z)-2-(fur-2-yl)-2-methoxyiminoacetamido]ceph-3-em-4-carboxylic acid, potassium salt (2.772 g, 6 mmole) in purified N,N dimethylformamide (18 ml). The mixture was allowed to react for 15 minutes and was then worked up as described in Example 4 to give the slightly impure title compound (2.809 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04446317
出典データセットuspto-grants-1984_05
ORD IDord-5b20fdeb2ec84f16ac26925f939f7bc5
出典メモuspto-grants-1984_05