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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 660946생성일: 2026년 10월 25일

Cesium carbonate → 2-[4-(2-chloroethyl)-3-(4-chlorophenyl)-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl]-N-[2-(tri-fluoromethyl)benzyl]-acetamide

https://huagongshe.com/reaction/660946

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물1-Chloro-2-iodoethaneHCID 136438—
반응물2-[3-(4-chlorophenyl)-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl]-N-[2-(tri-fluoromethyl)benzyl]-acetamideHCID 136199109—
촉매Benzyl triethylammonium chlorideHCID 66133—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물2-[4-(2-chloroethyl)-3-(4-chlorophenyl)-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl]-N-[2-(tri-fluoromethyl)benzyl]-acetamideHCID 58012174—

반응 단계

500 mg (1.01 mmol) of 2-[3-(4-chlorophenyl)-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl]-N-[2-(trifluoromethyl)benzyl]-acetamide from Example 243A are dissolved in 10 ml of toluene with 230 mg (1.01 mmol) of benzyltriethylammonium chloride. Next, a solution of 658 mg (2.02 mmol) of caesium carbonate, dissolved in 1.0 ml water, is added, and the mixture vigorously stirred at RT for 30 mins. After addition of 1.92 g (10.13 mmol) of 1-iodo-2-chloroethane, the mixture is heated for 7 hrs at 80° C. with vigorous stirring. The suspension is then diluted with ethyl acetate and washed once each with water, 10% sodium thiosulphate and saturated ammonium chloride solution. The organic phase is dried over sodium sulphate, filtered and concentrated in vacuo. The crude product is purified by preparative HPLC [Method 9]. 195 mg (41% of theory) of the target compound are thus obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08084481B2
출처 데이터셋uspto-grants-2011_12
ORD IDord-58b966efd83d47ffb5ab1a4a392881fc
출처 메모uspto-grants-2011_12