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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 280814생성일: 2026년 10월 25일

Hydrochloric Acid → Methyl 2-[[[4-(1-carboxyethoxy)-6-methyl-1,3,5-triazin-2-yl]aminocarbonyl]aminosulfonyl]benzoate

https://huagongshe.com/reaction/280814

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium HydroxideHCID 14798—
반응물Sulphonyl diisocyanateHCID 77898—
반응물Benzoic acid, 2-(isocyanatosulfonyl)-, methyl esterHCID 156281—
반응물Ethyl 2-[(4-amino-6-methyl-1,3,5-triazin-2-yl)oxy]propanoateHCID 19881799—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물Methyl 2-[[[4-(1-carboxyethoxy)-6-methyl-1,3,5-triazin-2-yl]aminocarbonyl]aminosulfonyl]benzoateHCID 1364675023.8%

반응 단계

Methyl 2-(isocyanatosulfonyl)benzoate (10.1 g) and 8.0 g of ethyl 2-[(4-amino-6-methyl-1,3,5-triazin-2-yl)-oxy]propanoate were stirred in 80 ml of methylene chloride at ambient temperature for 18 hours. An additional 2 g of the sulfonylisocyanate was added and the reaction mixture was stirred for four more hours and then 2 g more of the sulfonylisocyanate was added. After stirring for four more hours at ambient temperature, 400 ml of water was added and the pH of this mixture was adjusted to pH 8 by the addition of 10% aqueous sodium hydroxide. The aqueous phase was separated and acidified to pH 1 with hydrochloric acid to precipitate a thick white gum. Sufficient 50% aqueous sodium hydroxide was added to achieve pH 12 and the mixture was heated on a steam bath until a clear solution resulted. The solution was again acidified with hydrochloric acid to pH 3 and the resultant cloudy solution was extracted with dichloromethane. The organic phase was dried and the solvent was removed to afford 3.7 g of the title compound as a glass.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04591378
출처 데이터셋uspto-grants-1986_05
ORD IDord-f16119571d7047ceb03c09aad7a2a8b5
출처 메모uspto-grants-1986_05