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HRID 224215作成日:2026年10月27日

Phenylsulphonyl isocyanate → N-[(4-Dimethylamino-6-methylpyrimidin-2-yl)aminocarbonyl]benzenesulfonamide

https://huagongshe.com/reaction/224215

反応式

関与物質

役割名称HCID仕込み量
反応物Phenylsulphonyl isocyanateHCID 76096—
反応物N4,N4,6-trimethylpyrimidine-2,4-diamineHCID 13729300—
溶媒AcetoneHCID 180—
溶媒DichloromethaneHCID 6344—
生成物N-[(4-Dimethylamino-6-methylpyrimidin-2-yl)aminocarbonyl]benzenesulfonamideHCID 23332186—

反応手順

To a suspension of 15.2 g of 2-amino-4-dimethylamino-6-methylpyrimidine in 400 ml of methylene chloride at ambient temperature was added slowly 18.3 g of benzenesulfonylisocyanate. After stirring for four hours the mixture was stripped in-vacuo and the white semisolid residue triturated with ethyl ether and isolated by filtration. The solid was then slurried in hot acetone, cooled and refiltered to yield the solid named above which decomposed at 180°-182°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04231784
出典データセットuspto-grants-1980_11
ORD IDord-b4614a42cfa24a8fbd0ddc680ef7c32b
出典メモuspto-grants-1980_11