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HRID 1377950作成日:2026年10月25日

Dimethylformamide → methyl (E)-2-(2-dimethylaminomethylidenaminothiazol-4-yl)-2-methoxyiminoacetate

https://huagongshe.com/reaction/1377950

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物TetrahydrofuranHCID 8028—
反応物Sodium HydroxideHCID 14798—
反応物Phosphorus oxychlorideHCID 24813—
反応物(alphaZ)-2-Amino-alpha-(methoxyimino)-4-thiazoleacetic acidHCID 5486924—
溶媒MethanolHCID 887—
生成物methyl (E)-2-(2-dimethylaminomethylidenaminothiazol-4-yl)-2-methoxyiminoacetateHCID 8675085394%

反応条件

温度5 °C

反応手順

(Z)-2-(2-aminothiazol-4-yl)-2-methoxyiminoacetic acid (0.5 g, 2.5 mmol) was dissolved in 20 ml of tetrahydrofuran. Subsequent to the addition of 0.72 g (9.9 mmol) of dimethylformamide, the resulting solution was cooled to 5° C. The solution was added with 1.52 g (9.9 mmol) of phosphorus oxychloride and the resulting mixture was stirred for 3 hours. Methanol (20 ml) was added to the reaction mixture, followed by stirring for 10 minutes. A 2N aqueous solution of sodium hydroxide was added to the reaction mixture to adjust its pH to 7. The reaction mixture so obtained was extracted three times with 100 ml portions of chloroform. The organic phases were combined and then dried. The solvent was distilled off under reduced pressure. The residue was purified by chromatography on a silica gel column, whereby 0.63 g of the title compound was obtained (yield: 94%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05665888
出典データセットuspto-grants-1997_09
ORD IDord-45376663b3b1453e9a478de5a12b859b
出典メモuspto-grants-1997_09