HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetaldehyde → Methyl imidazo(1,2-a)pyridine-6-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetaldehyde | HCID 33 | — |
| Reactant | Methyl 6-aminonicotinate | HCID 737487 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Methyl imidazo(1,2-a)pyridine-6-carboxylate | HCID 2764326 | — |
Reaction Steps
To a solution of 50% aq. chloroacetaldehyde (1.1 eq, 36 mmol, 4.6 ml) in ethanol (120 ml) is added 6-amino-nicotinic acid methyl ester (1 eq, 33 mmol, 5 g) at room temperature. The reaction mixture is heated at reflux for 18 hours. The solvent is removed in vacuo and the crude product is dissolved in water (400 ml). The aqueous solution is treated with sodium bicarbonate to pH=8 and extracted with DCM (3×250 ml). The organic layer is dried (MgSO4) and evaporated to give the title compound as a beige solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08367662B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-698543befdbd4076a94a7c188b555497 |
| Source note | uspto-grants-2013_02 |