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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2047597Generated: October 31, 2026

5-Bromo-2,3-dimethoxypyridine → 5,6-Dimethoxypyridine-3-carbonitrile

https://huagongshe.com/reaction/2047597

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-2,3-dimethoxypyridineHCID 12563084—
ReactantHCID 178418546HCID 178418546—
SolventDimethylformamideHCID 6228—
Product5,6-Dimethoxypyridine-3-carbonitrileHCID 46736759—

Reaction Conditions

Temperature18 °C

Reaction Steps

To a solution of 5-bromo-2,3-dimethoxypyridine (4-2, 0.300 g, 1.38 mmol, 1.0 equiv) in dimethylformamide (3.9 mL) was added copper (I) cyanide (0.15 gL, 1.65 mmol, 1.2 equiv) and the reaction mixture was heated for 40 minutes at 18° C. in a microwave reactor. The reaction mixture was cooled and partitioned between EtOAc (50 mL) and water (50 mL). The organic phase was washed with water (2×30 mL) and brine (1×30 mL), dried over magnesium sulfate and concentrated. The residue was purified via normal phase chromatography (0 to 40% EtOAc in hexanes, silica) to afford the desired product (4-3) as white solid after concentration. ESI+MS[M+H]+C8H8N2O2 calc'd 165.1. found 165.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592457B2
Source datasetuspto-grants-2013_11
ORD IDord-f3d56d35b8d94f3ca2295f5a827bf4c8
Source noteuspto-grants-2013_11