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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1468779생성일: 2026년 10월 26일

Potassium Carbonate → 2-[4-(1-Methyl-6-oxo-1,6-dihydro-[4,4']bipyrimidinyl-2-yloxy)piperidin-1-yl]benzaldehyde

https://huagongshe.com/reaction/1468779

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물o-FluorobenzaldehydeHCID 67970—
반응물1-methyl-2-(piperidin-4-yloxy)-1H-[4,4']bipyrimidinyl-6-oneHCID 67977650—
용매Dimethyl SulfoxideHCID 679—
생성물2-[4-(1-Methyl-6-oxo-1,6-dihydro-[4,4']bipyrimidinyl-2-yloxy)piperidin-1-yl]benzaldehydeHCID 8666914652.3%

반응 조건

온도120 °C

반응 단계

To a mixture of 1-methyl-2-(piperidin-4-yloxy)-1H-[4,4′]bipyrimidinyl-6-one (1.00 g, 3.48 mmol) and 2-fluorobenzaldehyde (475 mg, 3.83 mmol) in dimethyl sulfoxide (3.50 ml) was added potassium carbonate (1.44 g, 10.4 mmol). The mixture was stirred at 120° C. for 4 hours. The mixture was partitioned between water and chloroform. The organic layer was washed with water (three times), dried over sodium sulfate, and concentrated in vacuo. The residue was purified by silica gel column chromatography (eluent; ethyl acetate) to afford 2-[4-(1-methyl-6-oxo-1,6-dihydro-[4,4′]bipyrimidinyl-2-yloxy)piperidin-1-yl]benzaldehyde as a yellow solid (711 mg, 1.82 mmol, 52%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09006232B2
출처 데이터셋uspto-grants-2015_04
ORD IDord-0fee3f999b644fa2b2ef5dd27ce5ed67
출처 메모uspto-grants-2015_04