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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1274650생성일: 2026년 10월 26일

Dichloromethane → 3-[3-[(Ethoxymethoxy)methyl]-1,2-benzisothiazol-5-yl]-1-methyl-6-(trifluoromethyl)-2,4(1H,3H)-pyrimidinedione

https://huagongshe.com/reaction/1274650

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물Chloromethyl ethyl etherHCID 18523—
반응물DiisopropylethylamineHCID 81531—
반응물3-[3-(hydroxymethyl)-1,2-benzisothiazol-5-yl]-1-methyl-6-(trifluoromethyl)-2,4(1H,3H)-pyrimidinedioneHCID 22119821—
용매Diethyl EtherHCID 3283—
생성물3-[3-[(Ethoxymethoxy)methyl]-1,2-benzisothiazol-5-yl]-1-methyl-6-(trifluoromethyl)-2,4(1H,3H)-pyrimidinedioneHCID 22119844—

반응 단계

To a mixture of 3-[3-(hydroxymethyl)-1,2-benzisothiazol-5-yl]-1-methyl-6-(trifluoromethyl)-2,4(1H,3H)-pyrimidinedione (0.800 g, 0.00224 mol) and methylene chloride is added ethyldiisopropylamine (0.780 ml, 0.00448 mol) followed by chloromethyl ethyl ether (0.310 ml, 0.00336 mol). The resultant mixture is stirred 42.5 hours at room temperature, diluted with ether, washed sequentially with 1 M aqueous hydrochloric acid, saturated sodium bicarbonate and brine, dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo to a yellow syrup. The syrup is chromatographed on silica gel with hexanes:ethyl acetate to give the product as a white solid which is identified by NMR spectral analysis.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06156700
출처 데이터셋uspto-grants-2000_12
ORD IDord-ddb3fbe77182416c926ff1265cfa9adf
출처 메모uspto-grants-2000_12