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HRID 27343作成日:2026年10月26日

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

https://huagongshe.com/reaction/27343

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Benzenesulfonyl isocyanate, 2-chloro-HCID 174071—
溶媒DichloromethaneHCID 6344—
生成物N-[(2,6-dimethoxypyrimidin-4-yl)aminocarbonyl]-2-chlorobenzenesulfonamideHCID 23342473—

反応手順

To a mixture of 1.10 g of 4-amino-2,6-dimethoxypyrimidin in 40 ml methylene chloride at ambient temperature and pressure was added 1.60 g of 2-chlorobenzenesulfonylisocyanate. The reaction was stirred 30 minutes and then refluxed an additional 15 minutes. Volatiles were removed under reduced pressure and the solid thereby obtained was washed with a little diethyl ether; yield 2.30 g, m.p. 193°-196°.

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-dc0ef96fde264f85bd4f5a6f0715efca
出典メモuspto-grants-1980_09