HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 6-Chloro-2-(4-cyclopropyl-1-piperazinyl)-pyrazine hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2,6-Dichloropyrazine | HCID 78504 | — |
| Reactant | 1-Cyclopropylpiperazine | HCID 4742004 | — |
| Solvent | 2,2,2-Trifluoroethanol | HCID 6409 | — |
| Solvent | Isopropanol ethanol | HCID 22179027 | — |
| Product | 6-Chloro-2-(4-cyclopropyl-1-piperazinyl)-pyrazine hydrochloride | HCID 20396004 | 36.1% |
Reaction Steps
Crude N-cyclopropylpiperazine (2.8 g) and 2,6-dichloropyrazine (3.0 g) are combined in 5 ml 2,2,2-trifluoroethanol and the mixture refluxed 4 hours under N2. The mixture is concentrated under vacuum and the residue partitioned between aqueous sodium carbonate and methylene chloride. The combined methylene chloride extracts are extracted with dilute hydrochloric acid which is made basic with sodium hydroxide. The crude base is extracted with methylene chloride and chromatographed on silica gel. Elution with CHCl3 gives fractions containing 2.4 g pure title base which is treated with hydrogen chloride in ethanol-isopropanol to give 2.0 g of the title salt, mp greater than 340° C. with decomposition at 245° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04163849 |
| Source dataset | uspto-grants-1979_08 |
| ORD ID | ord-ec0c6b84233c4a05821a31509b43171e |
| Source note | uspto-grants-1979_08 |