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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 14525생성일: 2026년 10월 23일

Dimethylformamide → 4-(2-Butynyloxy)-6-piperidinopyrimidine

https://huagongshe.com/ko/reaction/14525

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물PiperidineHCID 8082—
반응물Potassium CarbonateHCID 11430—
반응물4-(2-Butynyloxy)-6-chloropyrimidineHCID 12137602—
용매Ethyl AcetateHCID 8857—
생성물4-(2-Butynyloxy)-6-piperidinopyrimidineHCID 5934111677.1%

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 85 mg of piperidine was added therein, and the mixture was stirred for 5 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 178 mg of 4-(2-butynyloxy)-6-piperidinopyrimidine (hereinafter, referred to as Compound (16)).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732448B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-f5009c6f621b42c18ff9760b3dfadcbd
출처 메모uspto-grants-2010_06