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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2402309Generated: October 31, 2026

Benzyl Bromide → Benzyl 6-aminopyridine-3-carboxylate

https://huagongshe.com/reaction/2402309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant6-Aminonicotinic acidHCID 18496—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductBenzyl 6-aminopyridine-3-carboxylateHCID 4579094753.5%

Reaction Steps

Benzyl bromide (0.86 ml, 7.9 mmol) was added to a mixture of 6-aminonicotinic acid (1.0 g, 7.2 mmol) and potassium carbonate (1.5 g, 10.8 mmol) in DMF (4 mL). The mixture was stirred at room temperature for 16 hr and diluted with water (50 mL). The aqueous mixture was extracted with ethyl acetate (1×). The EtOAc layer was washed with brine, dried over MgSO4 and concentrated to provide crude solid product. Recrystallization from diethyl ether provided the title compound as a pale yellow solid (0.88 g, 53%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796313B2
Source datasetuspto-grants-2014_08
ORD IDord-347978c0d2ce4815a3c492a313de4ede
Source noteuspto-grants-2014_08