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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1274615생성일: 2026년 10월 26일

Hydrochloric Acid → 5-[3,6-Dihydro-3-methyl-2,6-dioxo-4-(trifluoromethyl)-1(2H)-pyrimidinyl]-N-(methylsulfonyl)-1,2-benzisothiazole-3-carboxamide

https://huagongshe.com/reaction/1274615

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물MethanesulfonamideHCID 72879—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물5-[3,6-Dihydro-3-methyl-2,6-dioxo-4-(trifluoromethyl)-1(2H)-pyrimidinyl]-1,2-benzisothiazole-3-carboxylic acidHCID 11187860—
용매TetrahydrofuranHCID 8028—
용매Acetic acid methylene chlorideHCID 21922555—
생성물5-[3,6-Dihydro-3-methyl-2,6-dioxo-4-(trifluoromethyl)-1(2H)-pyrimidinyl]-N-(methylsulfonyl)-1,2-benzisothiazole-3-carboxamideHCID 2211999772.3%

반응 단계

A solution of 5-[3,6-dihydro-3-methyl-2,6-dioxo-4-(trifluoromethyl)-1(2H)-pyrimidinyl]-1,2-benzisothiazole-3-carboxylic acid (0.400 g, 1.08 mmol) in tetrahydrofuran is treated with 1,1'-carbonyldiimidazole (0.260 g, 1.58 mmol), stirred at room temperature for 30 minutes, refluxed for 2 hours, cooled to room temperature, treated dropwise with a solution of methanesulfonamide (0.130 g, 1.37 mmol) and 1,8-diazabicyclo[5.4.0]undec-7-ene (0.230 g, 1.50 mmol), stirred at room temperature for 3 hours, and poured into 0.5 N hydrochloric acid. The resultant aqueous mixture is extracted with methylene chloride. The organic extracts are combined, washed with brine, dried over anhydrous sodium sulfate, and concentrated in vacuo to obtain a residue. Column chromatography of the residue using silica gel and a methylene chloride/acetic acid solution (10:1) gives the title product as a white solid (0.350 g, 72%, mp 241-243° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06156700
출처 데이터셋uspto-grants-2000_12
ORD IDord-3c35b67a1f5a4363ac9f09f1978e0b75
출처 메모uspto-grants-2000_12