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HRID 1195590作成日:2026年10月27日

Phosphorus oxychloride → HCID 131714064、化合物

https://huagongshe.com/reaction/1195590

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Acetamide, 2-(trimethylsilyl)-HCID 357676—
反応物7-Amino-3vinyl-3-cephem-4-carboxylic acidHCID 12818006—
反応物2-(p-Nitrobenzyloxycarbonylmethoxyimino)-2-(2-formamidothiazol-4-yl)acetic acidHCID 54535272—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物HCID 131714064HCID 13171406473.4%

反応手順

Vilsmeir reagent was prepared from N,N-dimethylformamide (1.67 ml) and phosphorus oxychloride (1.98 ml) in dry tetrahydrofuran (50.4 g) in a conventional manner. 2-(p-Nitrobenzyloxycarbonylmethoxyimino)-2-(2-formamidothiazol-4-yl)acetic acid (syn isomer) (7.35 g) was added to the stirred suspension of Vilsmeir reagent under ice-cooling, followed by stirring for 30 minutes at the same temperature. To a solution of 7-amino-3vinyl-3-cephem-4-carboxylic acid (3.4 g) and trimethylsilylacetamide (11.8 g) in ethyl acetate (35 ml) was added the activated acid solution obtained above at -20° C., and the reaction mixture was stirred at -20° C. to -10° C. for an hour. After water and ethyl acetate were added to the resultant solution, the separated organic layer was washed with water and then dried. A conventional work-up of the solution gave 7-[2-(p-nitrobenzyloxycarbonylmethoxyimino)-2-(2-formamidothiazol-4-yl)acetamido]-3-vinyl-3cephem-4-carboxylic acid (syn isomer) (6.8 g) as yellowish powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05110921
出典データセットuspto-grants-1992_05
ORD IDord-3f8045fff61a44bdb9e23ad6fde13c22
出典メモuspto-grants-1992_05