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HRID 27342作成日:2026年10月24日

2,6-Dimethoxy-4-aminopyrimidine → N-[(2,6-dimethoxypyrimidin-4-yl)aminocarbonyl]-2-methylbenzenesulfonamide

https://huagongshe.com/ja/reaction/27342

反応式

関与物質

役割名称HCID仕込み量
反応物2,6-Dimethoxy-4-aminopyrimidineHCID 76789—
反応物o-Toluenesulfonyl IsocyanateHCID 2733313—
溶媒DichloromethaneHCID 6344—
生成物N-[(2,6-dimethoxypyrimidin-4-yl)aminocarbonyl]-2-methylbenzenesulfonamideHCID 23342477—

反応手順

To a stirred mixture of 2.40 g of 4-amino-2,6-dimethoxypyrimidine in 40 ml methylene chloride at ambient temperature and pressure was slowly added 3.0 g of 2-methylbenzenesulfonylisocyanate. The reaction was stirred 40 minutes, filtered, and the solid thereby obtained was washed with a small amount of acetonitrile; yield 4.0 g, m.p. 174°-175°, NMR (DMSO-d6) relative to tetramethylsilane: δ 2.77, S, area 30; δ 4.05, S, area 60; δ 6.85, S, area 89; δ 7.7-8.6, multiplets, area 45; δ 10.00, S, area 9.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04221585
出典データセットuspto-grants-1980_09
ORD IDord-f3ed94953db04dcfa87506272299f2c5
出典メモuspto-grants-1980_09