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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 80Generated: October 23, 2026

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

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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantMethyl 4-((3-bromopyridin-2-yl)methoxy)benzoateHCID 68725036—
ReagentCesium carbonateHCID 10796—
CatalystBinap, (A+-)-HCID 634876—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventDimethylacetamideHCID 31374—
ProductMethyl 4-((3-(4-methylpiperazin-1-yl)pyridin-2-yl)methoxy)benzoateHCID 6872467164.22%

Reaction Conditions

Temperature100 °C

Reaction Steps

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 %).

Provenance & Evidence

Source dataset750 AstraZeneca ELN dataset
ORD IDord-78ee6abad7ea4585a19ca47439cdac57
Source note750 AstraZeneca ELN dataset