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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49005생성일: 2026년 10월 23일

Dichloromethane → 3-[3-(1,3-Dioxolan-2-yl)-1,2-benzisothiazol-5-yl]-1-methyl-6-(trifluoromethyl)uracil

https://huagongshe.com/ko/reaction/49005

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물DimethoxymethaneHCID 8020—
반응물3-[3-(dibromomethyl)-1,2-benzisothiazol-5-yl]-1-methyl-6-(trifluoromethyl)-2,4(1H,3H)-pyrimidinedioneHCID 22119839—
촉매Silver(I) trifluoromethanesulfonateHCID 76223—
용매Ethylene GlycolHCID 174—
생성물3-[3-(1,3-Dioxolan-2-yl)-1,2-benzisothiazol-5-yl]-1-methyl-6-(trifluoromethyl)uracilHCID 2063420217.5%

반응 단계

A mixture of 3-[3-(dibromomethyl)-1,2-benzisothiazol-5-yl]-1-methyl-6-(trifluoromethyl)-2,4(1H,3H)-pyrimidinedione (0.500 g, 10.0 mmol), silver trifluoromethanesulfonate (0.500 g, 19.5 mmol), ethylene glycol (5.00 ml), dichloromethane and dimethoxymethane is stirred three days at room temperature and treated with additional silver trifluoromethanesulfonate (0.300 g, 11.7 mmol). The resultant mixture is stirred one day at room temperature and treated with additional silver trifluoromethanesulfonate (0.400 g, 15.6 mmol) and ethylene glycol (1.00 ml), stirred another day at room temperature and treated again with silver trifluoromethanesulfonate (0.300 g, 11.7 mmol) and ethylene glycol (1.0 ml). After stirring an additional day the mixture is filtered. The filtrate is diluted with dichloromethane, washed with water, dried over anhydrous magnesium sulfate and concentrated in vacuo. The residue is triturated with hexanes-ethyl acetate to afford the title compound as a white solid (0.070 g, 17.5%, mp 213-216° C.) which is identified by NMR spectral analysis.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06706663B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-16b4da2259f54c529f075d0511a069de
출처 메모uspto-grants-2004_03