HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetaldehyde → 6-Chloroimidazo(1,2-a)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetaldehyde | HCID 33 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 5-Amino-2-chloropyridine | HCID 79305 | — |
| Product | 6-Chloroimidazo(1,2-a)pyridine | HCID 2764328 | — |
Reaction Steps
To a solution of 50% aq. chloroacetaldehyde (1.1 eq, 291 mmol, 37 ml) in ethanol (700 ml) is added 3-amino-6-chloro-pyridine (1 eq, 264 mmol, 34 g) at room temperature. The reaction mixture is refluxed for 3 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 a brown solid (39.2 g) 6-chloro-imidazo[1,2-a]pyridine; [M+H]+153(155)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08367662B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-9e04716f52c14a95aa5b45a01dacfbd8 |
| Source note | uspto-grants-2013_02 |