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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 463979생성일: 2026년 10월 23일

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/ko/reaction/463979

반응식

참여 물질

역할이름HCID투입량
반응물2-Amino-4-methoxy-6-methyl-1,3,5-triazineHCID 15466—
반응물2-(beta-Chloroethoxycarbonyl)benzenesulfonylisocyanateHCID 13920549—
용매DichloromethaneHCID 6344—
생성물N-[(4-Methoxy-6-methyl-1,3,5-triazin-2-yl)aminocarbonyl]-2-(2-chloroethoxycarbonyl)benzenesulfonamideHCID 1317669680.1%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04545808
출처 데이터셋uspto-grants-1985_10
ORD IDord-ba155e02318c41a7a7f94851178ed445
출처 메모uspto-grants-1985_10