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HRID 256266作成日:2026年10月26日

2-Thiophenecarboxylic acid, 3-(isocyanatosulfonyl)-, methyl ester → Methyl 3-[[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]aminosulfonyl]-2-thiophenecarboxylate

https://huagongshe.com/reaction/256266

反応式

関与物質

役割名称HCID仕込み量
反応物2-Thiophenecarboxylic acid, 3-(isocyanatosulfonyl)-, methyl esterHCID 157296—
反応物4-Methoxy-6-methylpyrimidin-2-amineHCID 587236—
溶媒AcetonitrileHCID 6342—
生成物Methyl 3-[[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]aminosulfonyl]-2-thiophenecarboxylateHCID 13390184—

反応手順

To 1.4 g of 2-amino-4-methoxy-6-methylpyrimidine in 30 ml of anhydrous acetonitrile was added at ambient temperature, with stirring 3.6 g of 2-methoxycarbonyl-3-thiophenesulfonylisocyanate. The mixture was heated to the boiling point and then allowed to cool to ambient temperature. After stirring for sixteen hours the precipitate present in the mixture was filtered off and washed with anhydrous ethyl ether. The product thus obtained which melted at 165°-173° showed absorption peaks by infrared spectroscopy at 1720 and 1700 cm-1, consistent for the carbonyl groups in the desired product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04701535
出典データセットuspto-grants-1987_10
ORD IDord-71fdcd695fb245e8be245884ebf3a9da
出典メモuspto-grants-1987_10