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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1164290생성일: 2026년 10월 25일

Isopropanol → (1-Methylethyl) [3-[[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]aminosulfonyl]phenyl]carbamate

https://huagongshe.com/reaction/1164290

반응식

참여 물질

역할이름HCID투입량
반응물IsopropanolHCID 3776—
반응물4-Methoxy-6-methylpyrimidin-2-amineHCID 587236—
반응물m-Isocyanatobenzenesulfonyl isocyanateHCID 13138205—
반응물3-isocyanato-N-[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]benzenesulfonamideHCID 20455869—
용매DichloromethaneHCID 6344—
생성물(1-Methylethyl) [3-[[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]aminosulfonyl]phenyl]carbamateHCID 13138206—

반응 단계

To an anhydrous solution of 2.3 g of m-isocyanatobenzenesulfonyl isocyanate in 50 ml of methylene chloride was added in small portions 1.4 g of 2-amino-4-methoxy-6-methylpyrimidine. Efficient stirring was maintained during the addition and for three additional hours. The intermediate thus obtained, 3-isocyanato-N-[(4-methoxy-6-methylpyrimidin-2-yl)aminocarbonyl]benzenesulfonamide, was reacted further by adding one gram of 2-propanol and stirring the resultant mixture for an additional sixteen hours. Filtration of the reaction mixture and evaporation of the filtrate yielded the desired product melting at 173°-180°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04369058
출처 데이터셋uspto-grants-1983_01
ORD IDord-43743f733122421eaa4b7bf0155caea8
출처 메모uspto-grants-1983_01