HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromopyruvate → ethyl imidazo[1,2-a]pyrazine-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromopyruvate | HCID 66144 | — |
| Reactant | Aminopyrazine | HCID 78747 | — |
| Product | ethyl imidazo[1,2-a]pyrazine-2-carboxylate | HCID 11845418 | 25% |
Reaction Steps
This derivative is obtained according to the technique described in Example 3, stage B, by reacting 2-aminopyrazine and ethyl bromopyruvate. Ethyl imidazo[1,2-a]pyrazine-2-carboxylate (m.p. 179° C., Yld=25%) is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05028605 |
| Source dataset | uspto-grants-1991_07 |
| ORD ID | ord-2838e3732f6b4bc7a020201c317b5fe9 |
| Source note | uspto-grants-1991_07 |