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HRID 80作成日:2026年10月23日

1-Methylpiperazine → Methyl 4-((3-(4-methylpiperazin-1-yl)pyridin-2-yl)methoxy)benzoate

https://huagongshe.com/ja/reaction/80

反応式

関与物質

役割名称HCID仕込み量
反応物1-MethylpiperazineHCID 53167—
反応物Methyl 4-((3-bromopyridin-2-yl)methoxy)benzoateHCID 68725036—
試薬Cesium carbonateHCID 10796—
触媒Binap, (A+-)-HCID 634876—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒DimethylacetamideHCID 31374—
生成物Methyl 4-((3-(4-methylpiperazin-1-yl)pyridin-2-yl)methoxy)benzoateHCID 6872467164.22%

反応条件

温度100 °C

反応手順

A mixture of methyl 4-((3-bromopyridin-2-yl)methoxy)benzoate (360 mg, 1.12 mmol), Pd2dba3 (205 mg, 0.22 mmol), BINAP (278 mg, 0.45 mmol), cesium carbonate (728 mg, 2.23 mmol) and 1-methylpiperazine (168 mg, 1.68 mmol) in DMA (10 mL) was stirred at 100 °C for overnight. Sat. NaHCO3 aq was added to the mixture, extracted with ethyl acetate three times, the combined organics were dried over anhydrous Na2SO4, filtered, the filtrate was conc. in vacuo, the residue was purified with ISCO (50% ethyl acetate in hexant to 100% ethyl acetate to 40% mthanol in ethyl acetate) to yield a brown oil as methyl 4-((3-(4-methylpiperazin-1-yl)pyridin-2-yl)methoxy)benzoate (245 mg, 64.2 %).

情報源と証拠

出典データセット750 AstraZeneca ELN dataset
ORD IDord-78ee6abad7ea4585a19ca47439cdac57
出典メモ750 AstraZeneca ELN dataset