戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 569366作成日:2026年10月23日

Phosphorus oxychloride → Benzhydryl 7-(2-benzyloxycarbonylmethoxyimino-4-bromo-3-oxobutyramido)-3-vinyl-3-cephem-4-carboxylate

https://huagongshe.com/ja/reaction/569366

反応式

関与物質

役割名称HCID仕込み量
反応物Phosphorus oxychlorideHCID 24813—
反応物Chloro-N,N-dimethylformiminium chlorideHCID 77311—
反応物Acetamide, 2-(trimethylsilyl)-HCID 357676—
反応物Benzhydryl 7-amino-3vinyl-3cephem-4-carboxylate hydrochlorideHCID 12818005—
反応物2-Benzyloxycarbonylmethoxyimino-4-bromo-3-oxobutyric acidHCID 54032159—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物Benzhydryl 7-(2-benzyloxycarbonylmethoxyimino-4-bromo-3-oxobutyramido)-3-vinyl-3-cephem-4-carboxylateHCID 13171333174.5%

反応手順

Vilsmeier reagent prepared from N,N-dimethylformamide (0.67 ml) and phosphorus oxychloride (0.79 ml) was suspended in dry tetrahydrofuran (25 ml). Thereto was added 2-benzyloxycarbonylmethoxyimino-4-bromo-3-oxobutyric acid (2.8 g) at 0° C. with stirring, and the stirring was continued at 0° to 5° C. for an hour to prepare the activated acid solution. This activated acid solution was added at a time to a solution of benzhydryl 7-amino-3-vinyl-3-cephem-4-carboxylate hydrochloride (2.2 g) and trimethylsilylacetamide (7.0 g) in methylene chloride (30 ml) at -35° C., and the mixture was stirred at -10° to -5° C. for 30 minutes. The reaction mixture was poured into ethyl acetate (200 ml), and the separated organic solution was washed with a saturated aqueous sodium bicarbonate and a saturated aqueous sodium chloride, followed by drying over magnesium sulfate. Removal of the solvent gave benzhydryl 7-(2-benzyloxycarbonylmethoxyimino-4-bromo-3-oxobutyramido)-3-vinyl-3-cephem-4-carboxylate (2.8 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04731443
出典データセットuspto-grants-1988_03
ORD IDord-fe439d98f61542b2aa8425050489ac81
出典メモuspto-grants-1988_03