HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazo(1,2-a)pyrazine → 5,6,7,8-Tetrahydroimidazo(1,2-a)pyrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazo(1,2-a)pyrazine | HCID 2771670 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol hydrochloride | HCID 21887872 | — |
| Product | 5,6,7,8-Tetrahydroimidazo(1,2-a)pyrazine | HCID 13247046 | — |
Reaction Steps
Imidazo[1,2-a]pyrazine (250 mg, 2.1 mmol) and palladium on carbon (10%) (55.8 mg, 0.53 mmol) were placed in a pressure resistant bottle and suspended under nitrogen in 0.5M HCl/EtOH. The mixture was stirred under at 45 psi H2 for 16 hrs. LC/MS showed completion. The next day, the reaction mixture was passed through celite cake. The filtrate was concentrated under reduced pressure to afford a tan solid. This was used directly without further purification. MS: [N+H]=124.2; Calc'd for C6H9N3: 123.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07981891B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-6e4a85c1c31443be9c2b526c2ad8fc23 |
| Source note | uspto-grants-2011_07 |