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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 14528생성일: 2026년 10월 23일

Dimethylformamide → 4-(2-Butynyloxy)-6-(3-methylpiperidino) pyrimidine

https://huagongshe.com/ko/reaction/14528

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Potassium CarbonateHCID 11430—
반응물3-MethylpiperidineHCID 79081—
반응물4-(2-Butynyloxy)-6-chloropyrimidineHCID 12137602—
용매Ethyl AcetateHCID 8857—
생성물4-(2-Butynyloxy)-6-(3-methylpiperidino) pyrimidineHCID 5934114673.9%

반응 조건

온도80 °C

반응 단계

Into 2 ml of N,N-dimethylformamide was resolved 183 mg of 4-chloro-6-(2-butynyloxy)pyrimidine, 166 mg of potassium carbonate and 99 mg of 3-methylpiperidine was added therein, and the mixture was stirred for 4 hours at 80° C. The reaction mixture was cooled to near room temperature, ethyl acetate was added therein, and the mixture was washed with a saturated sodium chloride aqueous solution three times. The organic layers were dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography to obtain 181 mg of 4-(2-butynyloxy)-6-(3-methylpiperidino) pyrimidine (hereinafter, referred to as Compound (19)).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732448B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-b866f9dd667045cc8fad966c4332066d
출처 메모uspto-grants-2010_06