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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18678생성일: 2026년 10월 25일

N-Methylisopropylamine → 3-[4-Chloro-2-fluoro-5-{[isopropyl(methyl)amino]carbonylaminosulfonyl}phenyl]-1-methyl-2,4-dioxo-6-trifluoromethyl-1,2,3,4-tetrahydropyrimidine

https://huagongshe.com/reaction/18678

반응식

참여 물질

역할이름HCID투입량
반응물N-MethylisopropylamineHCID 78485—
반응물2-Chloro-4-fluoro-5-[3,6-dihydro-3-methyl-2,6-dioxo-4-trifluoromethyl-(2H)-pyrimidin-1-yl]benzenesulfonylisocyanateHCID 58709439—
용매1,2-DichloroethaneHCID 11—
생성물3-[4-Chloro-2-fluoro-5-{[isopropyl(methyl)amino]carbonylaminosulfonyl}phenyl]-1-methyl-2,4-dioxo-6-trifluoromethyl-1,2,3,4-tetrahydropyrimidineHCID 58709437—

반응 단계

With stirring, 1.0 g (2.34 mmol) of 2-chloro-4-fluoro-5-[3,6-dihydro-3-methyl-2,6-dioxo-4-trifluoromethyl-(2H)-pyrimidin-1-yl]benzenesulfonyl isocyanate in 1,2-dichloroethane was added to a solution of 0.34 g (4.68 mmol) of N-methylisopropylamine in 1,2-dichloroethane, and the mixture was stirred overnight. The reaction mixture was concentrated, the residue was taken up in methylene chloride and 0.5N hydrochloric acid was added. The organic phase was then dried and the solvent was removed. This gave 0.5 g (42% of theory) of the title compound as a colorless solid (m.p.: 145° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741485B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-dfb6cfc1a7aa40f98611b46339d471c2
출처 메모uspto-grants-2010_06