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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49003생성일: 2026년 10월 23일

1,4-Dioxane--water (1/1) → 5-[3,6-dihydro-3-methyl-2,6-dioxo-4-(trifluoromethyl)-1(2H)-pyrimidinyl]-1, 2-benzisothiazole-3-carboxaldehyde

https://huagongshe.com/ko/reaction/49003

반응식

참여 물질

역할이름HCID투입량
반응물1,4-Dioxane--water (1/1)HCID 21886435—
반응물3-[3-(dibromomethyl)-1,2-benzisothiazol-5-yl]-1-methyl-6-(trifluoromethyl)-2,4(1H,3H)-pyrimidinedioneHCID 22119839—
촉매Silver NitrateHCID 24470—
용매DichloromethaneHCID 6344—
생성물5-[3,6-dihydro-3-methyl-2,6-dioxo-4-(trifluoromethyl)-1(2H)-pyrimidinyl]-1, 2-benzisothiazole-3-carboxaldehydeHCID 17852368—

반응 단계

A solution of 3-[3-(dibromomethyl)-1,2-benzisothiazol-5-yl]-1-methyl-6-(trifluoromethyl)-2,4(1H,3H)-pyrimidinedione (0.500 g, 0.00100 mol) in a dioxane/water mixture (5:2) is treated with silver nitrate (0.340 g, 0.00200 mol), refluxed for 90 minutes, cooled to room temperature, stirred for 18 hrs, refluxed for three hrs, cooled, and filtered through a pad of diatomaceous earth. The resultant filtrate is concentrated in vacuo to obtain an aqueous mixture. The aqueous mixture is extracted with methylene chloride. The organic extract is washed sequentially with water and brine, dried over anhydrous magnesium sulfate, and concentrated in vacuo to obtain a solid. Column chromatography of the solid using silica gel and methylene chloride gives the title product as a solid (0.240 g, mp 193-194.5° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06706663B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-6b3cd572d4d840a59b547b957ebf8cee
출처 메모uspto-grants-2004_03