HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetaldehyde → Imidazo(1,2-a)pyrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetaldehyde | HCID 33 | — |
| Reactant | Aminopyrazine | HCID 78747 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Imidazo(1,2-a)pyrazine | HCID 2771670 | — |
Reaction Steps
A round bottom set up with reflux condenser was charged with pyrazin-2-amine (1000 mg, 10.52 mmol), 2-chloroacetaldehyde (˜50% wt) (2.03 ml, 31.55 mmol), and EtOH (23 mL) and heated under reflux overnight. Next day LC/MS showed completion. The mixture was concentrated and passed through a plug of silica (solvent used: 1% MeOH/DCM) to afford imidazo[1,2-a]pyrazine as off-white solid. MS [M+H]=120.1; Calc'd for C6H5N3: 119.1
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07981891B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-4bf59c1728684b9c8a5a313d1ca6f0d8 |
| Source note | uspto-grants-2011_07 |