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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 48969생성일: 2026년 10월 24일

Methanol → 3-[3-[3-(Methoxymethyl)-2-thienyl]-1,2-benzisothiazol-5-yl]-1-methyl-6-(trifluoromethyl)uracil

https://huagongshe.com/ko/reaction/48969

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물DichloromethaneHCID 6344—
반응물3-[3-[3-(Bromomethyl)-2-thienyl]-1,2-benzisothiazol-5-yl]-1-methyl-6-(trifluoromethyl)uracilHCID 20634213—
촉매SilverHCID 23954—
생성물3-[3-[3-(Methoxymethyl)-2-thienyl]-1,2-benzisothiazol-5-yl]-1-methyl-6-(trifluoromethyl)uracilHCID 2063421987.7%

반응 단계

To a mixture of 3-[3-[3-(bromomethyl)-2-thienyl]-1,2-benzisothiazol-5-yl]-1-methyl-6-(trifluoromethyl)uracil(1.00 g, 1.99 mmol), methylene chloride and methanol is added silver trifluorormethanesulfonate. The resultant white suspension is stirred overnight at room temperature and filtered through a pad of diatomaceous earth with methylene chloride wash. The filtrate is washed with saturated sodium bicarbonate and brine, dried over anhydrous magnesium sulfate and concentrated in vacuo to a pale yellow solid, which is recrystallized from diethyl ether to afford the title compound (0.790 g, 87.7%, mp 131-133° 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-0e0b7e61abf743bc944f045de8b3f7a3
출처 메모uspto-grants-2004_03