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HRID 1468779作成日:2026年10月27日

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

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物o-FluorobenzaldehydeHCID 67970—
反応物1-methyl-2-(piperidin-4-yloxy)-1H-[4,4']bipyrimidinyl-6-oneHCID 67977650—
溶媒Dimethyl SulfoxideHCID 679—
生成物2-[4-(1-Methyl-6-oxo-1,6-dihydro-[4,4']bipyrimidinyl-2-yloxy)piperidin-1-yl]benzaldehydeHCID 8666914652.3%

反応条件

温度120 °C

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09006232B2
出典データセットuspto-grants-2015_04
ORD IDord-0fee3f999b644fa2b2ef5dd27ce5ed67
出典メモuspto-grants-2015_04