HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazo(1,2-a)pyrazin-8-amine, 3-bromo-N-methyl- → N-Methylimidazo[1,2-A]pyrazin-8-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazo(1,2-a)pyrazin-8-amine, 3-bromo-N-methyl- | HCID 3088360 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-Methylimidazo[1,2-A]pyrazin-8-amine | HCID 10351844 | 158.8% |
Reaction Steps
To a solution of (3-bromo-imidazo[1,2-a]pyrazin-8-yl)-methyl-amine (Example 1) (2.4 g, 11.9 mmol) in methanol (160 ml) was added Pd-C (10% wt. 0.1 eq). The mixture was hydrogenated at rt overnight, filtered, and washed with hot methanol. The organics were combined and concentrated to afford 2.8 g of crude imidazo[1,2-a]pyrazin-8-yl-methyl-amine (M).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07186832B2 |
| Source dataset | uspto-grants-2007_03 |
| ORD ID | ord-54ee0e4aaf6b40548e7f26e62a8f6db0 |
| Source note | uspto-grants-2007_03 |