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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2069891생성일: 2026년 10월 27일

Potassium Carbonate → 4-(2-Butynyloxy)-6-(3-trifluoromethylpiperidino)pyrimidine

https://huagongshe.com/reaction/2069891

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물2-Butyn-1-olHCID 12991—
반응물4,6-DifluoropyrimidineHCID 137717—
반응물3-(Trifluoromethyl)pyrrolidineHCID 5152159—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매TriethylamineHCID 8471—
생성물4-(2-Butynyloxy)-6-(3-trifluoromethylpiperidino)pyrimidineHCID 57672951—

반응 조건

온도30 °C

반응 단계

To a mixture obtained by adding 110.0 g of 4,6-difluoropyrimidine, 132.3 g of potassium carbonate and 19.2 g of triethylamine to 220.0 g of toluene, 69.8 g of 2-butyn-1-ol is added dropwise at 25 to 30° C. over one hour, followed by stirring at 30° C. Then, 220.0 g of water is added dropwise into the reaction mixture, followed by stirring. Then, 152.4 g of 3-trifluoromethylpyrrolidine is added dropwise and, after the mixture is stirred at 30° C., the reaction mixture is allowed to stand. After separating into the organic layer and the aqueous layer, the aqueous layer is removed and the organic layer is washed once with 220.0 g of 5% hydrochloric acid and then washed once with 220.0 g of water. The organic layer is concentrated to obtain 4-(2-butynyloxy)-6-(3-trifluoromethylpiperidino)pyrimidine (hereinafter referred to as the present compound (2)).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08299245B2
출처 데이터셋uspto-grants-2012_10
ORD IDord-7e674331cfe14eaaafee9cbb79f9b92b
출처 메모uspto-grants-2012_10