HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1675949Generated: October 30, 2026
5-Bromo-2,3-dimethoxypyridine → 5,6-Dimethoxypyridine-3-carbonitrile
https://huagongshe.com/reaction/1675949
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Bromo-2,3-dimethoxypyridine | HCID 12563084 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5,6-Dimethoxypyridine-3-carbonitrile | HCID 46736759 | — |
Reaction Steps
To a solution of 5-bromo-2,3-dimethoxypyridine (7-2, 0.300 g, 1.38 mmol, 1.0 equiv) in dimethylformamide (3.9 mL) was added copper (I) cyanide (0.15 g, 1.65 mmol, 1.2 equiv) and the reaction mixture was heated for 40 minutes at 180° 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 (7-3) as white solid after concentration. ESI+MS [M+H]+ C8H8N2O2 calc'd 165.1, found 165.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08003797B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-705f7fee70e246cf8fc3d3a01c3a89a8 |
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| Source note | uspto-grants-2011_08 |
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