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HRID 383276作成日:2026年10月25日

Potassium Carbonate → 3-[2-(4-Fluoro-phenyl)-pyridin-4-yl]-7-[3-(3-piperidin-1-yl-propoxy)-phenyl]-imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/383276

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N-(3-chloropropyl)piperidine hydrochlorideHCID 79624—
反応物HCID 68482795HCID 68482795—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物3-[2-(4-Fluoro-phenyl)-pyridin-4-yl]-7-[3-(3-piperidin-1-yl-propoxy)-phenyl]-imidazo[1,2-a]pyridineHCID 25261102—

反応条件

温度60 °C

反応手順

3-{3-[2-(4-Fluoro-phenyl)-pyridin-4-yl]-imidazo[1,2-a]pyridin-7-yl}-phenol (Ex. 1.102) (1 eq, 0.131 mmol, 50 mg), 1-(3-chloropropyl)piperidine monohydrochloride (2.0 eq, 0.262 mmol, 53.7 mg) and potassium carbonate (3.0 eq, 0.394 mmol, 54.4 mg) are dissolved in DMF (4 ml) and heated at 60° C. for 16 h. The reaction mixture is diluted with CH2Cl2 and washed with NaHCO3 and brine. The organic phase is dried over MgSO4, filtered and evaporated to dryness. The reaction mixture is purified by flash chromatography on silica eluting with DCM/MeOH 7/3 to yield 3-[2-(4-fluoro-phenyl)-pyridin-4-yl]-7-[3-(3-piperidin-1-yl-propoxy)-phenyl]-imidazo[1,2-a]pyridine as a yellow solid; [M+H]+=507

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08367662B2
出典データセットuspto-grants-2013_02
ORD IDord-98e5661756e741f09696a294b7a185f6
出典メモuspto-grants-2013_02