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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 266248생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/266248

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참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물TetrahydrofuranHCID 8028—
반응물Sodium HydroxideHCID 14798—
반응물Phosphorus oxychlorideHCID 24813—
반응물(alphaZ)-2-Amino-alpha-(methoxyimino)-4-thiazoleacetic acidHCID 5486924—
용매MethanolHCID 887—
생성물methyl (E)-2-(2-dimethylaminomethylidenaminothiazol-4-yl)-2-methoxyiminoacetateHCID 8675085394%

반응 조건

온도5 °C

반응 단계

(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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05650518
출처 데이터셋uspto-grants-1997_07
ORD IDord-0da2f22b3d394e28aac059438636dbe2
출처 메모uspto-grants-1997_07