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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1274587생성일: 2026년 10월 26일

Methyl iodide → Ethyl 5-[3,6-dihydro-3-methyl-2,6-dioxo-4-(trifluoromethyl)-1(2H)-pyrimidinyl]-1,2-benzisothiazole-3-acetate

https://huagongshe.com/reaction/1274587

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Ethyl AcetateHCID 8857—
반응물Potassium CarbonateHCID 11430—
반응물Ethyl 5-[3,6-dihydro-2,6-dioxo-4-(trifluoromethyl)-1(2H)-pyrimidinyl]-1,2-benzisothiazole-3-acetateHCID 10960337—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물Ethyl 5-[3,6-dihydro-3-methyl-2,6-dioxo-4-(trifluoromethyl)-1(2H)-pyrimidinyl]-1,2-benzisothiazole-3-acetateHCID 1172934754.7%

반응 단계

A mixture of ethyl 5-[3,6-dihydro-2,6-dioxo-4-(trifluoromethyl)-1(2H)-pyrimidinyl]-1,2-benzisothiazole-3-acetate (0.643 g, 0.00160 mol) and potassium carbonate (0.243 g, 0.00170 mol) in N,N-dimethylformamide is stirred at room temperature for 90 minutes, treated with iodomethane (0.320 mL, 0.00500 mol), stirred at room temperature overnight, and diluted with water. The resultant aqueous mixture is extracted with methylene chloride. The organic extract is washed with water, dried over anhydrous magnesium sulfate, and concentrated in vacuo to obtain a brown oil. Column chromatography of the oil using silica gel and a 10% ethyl acetate in hexanes solution gives the title product as a tan solid (0.362 g, mp 150-152° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06156700
출처 데이터셋uspto-grants-2000_12
ORD IDord-8529716320824d78aad12efa8a24ab5c
출처 메모uspto-grants-2000_12