돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1759857생성일: 2026년 10월 27일

Potassium Carbonate → 4-(2,6-Difluorobenzyloxy)-6-(2-butynyloxy)pyrimidine

https://huagongshe.com/reaction/1759857

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Ammonium ChlorideHCID 25517—
반응물2,6-Difluorobenzyl alcoholHCID 87921—
반응물4-(2-Butynyloxy)-6-methanesulfonylpyrimidineHCID 22599863—
용매DimethylformamideHCID 6228—
생성물4-(2,6-Difluorobenzyloxy)-6-(2-butynyloxy)pyrimidineHCID 2259974472.8%

반응 조건

온도50 °C

반응 단계

To 2 ml of N,N-dimethylformamide were added 0.15 g of 4-(2-butynyloxy)-6-methanesulfonylpyrimidine, 0.14 g of potassium carbonate, and 0.16 g of 2,6-difluorobenzylalcohol, followed by stirring at 50° C. for 7 hours. The reaction mixture was then left for cooling to room temperature and poured into a saturated aqueous ammonium chloride solution, which was extracted three times with chloroform. The chloroform layers were combined, washed with diluted hydrochloric acid and then with water, and dried over anhydrous magnesium sulfate and then concentrated. The residue was subjected to silica gel column chromatography to give 0.14 g of 4-(2,6-difluorobenzyloxy)-6-(2-butynyloxy)pyrimidine (the present compound (68)).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06838463B2
출처 데이터셋uspto-grants-2005_01
ORD IDord-619733dd861b430381b8e5985bb58896
출처 메모uspto-grants-2005_01