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HRID 619914作成日:2026年10月27日

2,6-Dimethyl-4-aminopyrimidine → N-[(2,6-dimethylpyrimidin-4-yl)aminocarbonyl]2-methoxycarbonylbenzenesulfonamide

https://huagongshe.com/reaction/619914

反応式

関与物質

役割名称HCID仕込み量
反応物2,6-Dimethyl-4-aminopyrimidineHCID 68039—
反応物Benzoic acid, 2-(isocyanatosulfonyl)-, methyl esterHCID 156281—
溶媒AcetonitrileHCID 6342—
生成物N-[(2,6-dimethylpyrimidin-4-yl)aminocarbonyl]2-methoxycarbonylbenzenesulfonamideHCID 13176760—

反応手順

To a suspension of 1.2 g of 4-amino-2,6-dimethylpyrimidine in 30 ml of dry acetonitrile with stirring was added 2.4 g of 2-methoxycarbonylbenzenesulfonylisocyanate. The mixture was stirred for two hours at ambient temperature, allowed to stand for sixteen hours and the desired product, which had precipitated, was removed by filtration and washed with butyl chloride to yield 2.4 g, m.p. 125°-127°. The product showed absorption peaks by Nuclear Magnetic Resource at 4.0, 2.62 and 2.9 ppm; consistent for the product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04818278
出典データセットuspto-grants-1989_04
ORD IDord-dee5372393764a799b3ee4f631b03f71
出典メモuspto-grants-1989_04