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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1105993Generated: October 31, 2026

Dimethylformamide → 6-Oxo-1,6-dihydro-3,4'-bipyridine-5-carbonitrile

https://huagongshe.com/reaction/1105993

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPhosgeneHCID 6371—
Reactant4-MethylpyridineHCID 7963—
ReactantThiophosgeneHCID 10040—
ReactantThionyl ChlorideHCID 24386—
ReactantPhosphorus trichlorideHCID 24387—
ReactantPhosphorus tribromideHCID 24614—
ReactantSulfuryl chlorideHCID 24648—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantPhosphorus pentachlorideHCID 24819—
ReactantCarbonyl bromideHCID 79057—
SolventWaterHCID 962—
Product6-Oxo-1,6-dihydro-3,4'-bipyridine-5-carbonitrileHCID 131989—

Reaction Steps

The process which comprises the steps of reacting 4-picoline below about 30° C. with at least three mole equivalents per mole of 4-picoline of an inorganic acid halide selected from phosphorus oxychloride, phosgene, thionyl chloride, sulfuryl chloride, phosphorus trichloride, phosphorus pentachloride, phosphorus tribromide, carbonyl dibromide or thiophosgene and about five to twenty volumes of dimethylformamide per volume of 4-picoline, adding the reaction mixture to cold water and adjusting the pH to about 8.0 while keeping the temperature below about 30° C., filtering off the precipitated inorganic cationic salt, treating the aqueous filtrate which contains N-[3-dimethylamino-2-(4-pyridinyl)-2-propenylidene]-N-methylmethaniminium salt with at least about 30-35% molar excess of α-cyanoacetamide and at least three mole equivalents of base still keeping the temperature below about 30° C., and then isolating either 5-cyano-[3,4'-bipyridin]-6(1H)-one as its inorganic cationic salt or, after neutralization, in its free base form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04310670
Source datasetuspto-grants-1982_01
ORD IDord-91020b82470240b2909c915a5f3b3640
Source noteuspto-grants-1982_01