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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1592171생성일: 2026년 10월 26일

Potassium Carbonate → 4-(2-butynyloxy)-6-(N-ethyl-N-isopropylamino)pyrimidine

https://huagongshe.com/reaction/1592171

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물IsopropylethylamineHCID 88318—
반응물4-(2-Butynyloxy)-6-chloropyrimidineHCID 12137602—
용매DimethylformamideHCID 6228—
생성물4-(2-butynyloxy)-6-(N-ethyl-N-isopropylamino)pyrimidineHCID 2259972333.9%

반응 조건

온도60 °C

반응 단계

To 2 ml of N,N-dimethylformamide were added 183 mg of 4-chloro-6-(2-butynyloxy)pyrimidine, 166 mg of potassium carbonate, and 87 mg of N-ethylisopropylamine, followed by stirring at 60° C. for 7 hours. Then, 166 mg of potassium carbonate and 435 mg of N-ethylisopropylamine were added, and the mixture was stirred at 80° C. for 8 hours. Then, 166 mg of potassium carbonate and 435 mg of N-ethylisopropylamine were added, and the mixture was stirred at 120° C. for 5 hours. The reaction mixture was then left for cooling to room temperature and subjected to phase separation three times between ethyl acetate and an aqueous sodium chloride solution. The organic layer was dried over anhydrous magnesium sulfate and then concentrated. The residue was subjected to preparative silica gel thin layer chromatography to give 79 mg of 4-(2-butynyloxy)-6-(N-ethyl-N-isopropylamino)pyrimidine (the present compound (105)).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07291730B2
출처 데이터셋uspto-grants-2007_11
ORD IDord-ca65dded8548451db2beda9fcb0e7236
출처 메모uspto-grants-2007_11