Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 3-Pyridinecarboxaldehyde | HCID 10371 | — |
| Reactant | 3-(1H-Imidazol-2-yl)pyridine | HCID 12395500 | — |
| Reactant | (4-Methoxyphenyl)(oxo)acetaldehyde--water (1/1) | HCID 15556730 | — |
| Reactant | Sodium Acetate Trihydrate | HCID 23665404 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178488775 | HCID 178488775 | — |
Reaction Steps
A solution of sodium acetate trihydrate (5.8 g, 0.04 m), 3-pyridinecarboxaldehyde (2.3 g., 0.02 m), p-methoxyphenylglyoxal monohydrate (3.92 g., 0.02 m), water (20 ml.), concentrated aqueous ammonia (25 ml.), and methanol (75 ml.) is allowed to stand at room temperature overnight. The solution is concentrated to dryness under reduced pressure (20 mm) over steam, treated with saturated Na2CO3 (100 ml.) and extracted with chloroform (3 × 100 ml.). The organic layer is dried over Na2SO4, filtered and concentrated to dryness. The residue is chromatographed on silica gel (300 ml.) and the product eluted with 3-5% MeOH/CHCl3. The material is crystallized from acetonitrile to give 2.3 g. of 4-p-methoxyphenyl)-2-(3-pyridyl)imidazole of m.p. 184-186.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04134983 |
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| Source dataset | uspto-grants-1979_01 |
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| ORD ID | ord-28206df6ec19442b826490c85ea23990 |
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| Source note | uspto-grants-1979_01 |
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