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HRID 485514作成日:2026年10月27日

2-Amino-4-methoxy-6-methyl-1,3,5-triazine → N-[(4-Methoxy-6-methyl-1,3,5-triazin-2-yl)aminocarbonyl]-2-(2-chloroethoxycarbonyl)benzenesulfonamide

https://huagongshe.com/reaction/485514

反応式

関与物質

役割名称HCID仕込み量
反応物2-Amino-4-methoxy-6-methyl-1,3,5-triazineHCID 15466—
反応物2-(beta-Chloroethoxycarbonyl)benzenesulfonylisocyanateHCID 13920549—
溶媒DichloromethaneHCID 6344—
生成物N-[(4-Methoxy-6-methyl-1,3,5-triazin-2-yl)aminocarbonyl]-2-(2-chloroethoxycarbonyl)benzenesulfonamideHCID 1317669680.1%

反応手順

To 0.7 g of 2-amino-4-methoxy-6-methyl-1,3,5-triazine in 10 ml anhydrous methylene chloride solvent was added 1.45 g 2-(β-chloroethoxycarbonyl)benzenesulfonyl isocyanate with stirring at ambient temperature. The mixture was thereafter stirred for sixteen hours. The solvent was evaporated under reduced pressure and the residue triturated with hexane and filtered to yield 1.72 g of compound which melted at 167°-170° C. The solid showed infrared absorption peaks at 1700 and 1705 cm-1, consistent for N-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)aminocarbonyl]-2-(2-chloroethoxycarbonyl)benzenesulfonamide.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04536576
出典データセットuspto-grants-1985_08
ORD IDord-72e4de42911b4b32bfe7563ff02b5d0d
出典メモuspto-grants-1985_08