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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | 4-Methylpyridine | HCID 7963 | — |
| Reactant | Thiophosgene | HCID 10040 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Phosphorus trichloride | HCID 24387 | — |
| Reactant | Phosphorus tribromide | HCID 24614 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | Carbonyl bromide | HCID 79057 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Oxo-1,6-dihydro-3,4'-bipyridine-5-carbonitrile | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04310670 |
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| Source dataset | uspto-grants-1982_01 |
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| ORD ID | ord-91020b82470240b2909c915a5f3b3640 |
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| Source note | uspto-grants-1982_01 |
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