HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → HCID 12841593, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | HCID 12841587 | HCID 12841587 | — |
| Reactant | 8-Bromo-3-chloroimidazo[1,2-a]pyrazine | HCID 20299637 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 12841593 | HCID 12841593 | — |
Reaction Steps
To a solution of the mixture of 3,8-dichloroimidazo[1,2-a]pyrazine and 8-bromo-3-chloroimidazo[1,2-a]pyrazine obtained above in 25 ml of acetonitrile is added an excess amount of piperazine (5 g). After refluxing and isolation in essentially the same manner as Example 1, Step B, 3-chloro-8-(1-piperazinyl)-imidazo[1,2-a]pyrazine hydrochloride salt is obtained with m.p. >300° C. dec.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04242344 |
| Source dataset | uspto-grants-1980_12 |
| ORD ID | ord-9399a5c83c834b4dbc2ba942bd37d36b |
| Source note | uspto-grants-1980_12 |