HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → HCID 20299635, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | HCID 20299638 | HCID 20299638 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 20299635 | HCID 20299635 | — |
Reaction Steps
6-Chloro-3-trifluoromethylthioimidazo[1,2-a]pyrazine from Step A is reacted with piperazine (2 g) in efluxing acetonitrile for 24 hours. The mixture is cooled, concentrated under vacuum, and the esidue partitioned between dilute sodium hydroxide and chloroform. The chloroform extract is dried over sodium sulfate, filtered and concentrated under vacuum to the crude base which is purified by chromatography on silica gel and converted to 6-(1-piperazinyl)-3-trifluoromethylthioimidazo[1,2-a]pyrazine hydrochloride with ethanolic hydrogen chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04242344 |
| Source dataset | uspto-grants-1980_12 |
| ORD ID | ord-7524e5751b054103995019081c48b783 |
| Source note | uspto-grants-1980_12 |