HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 6-Chloro2-(4-allyl-1-piperazinyl)-pyrazine hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | MK-212 hydrochloride | HCID 198421 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Isopropanol ethanol | HCID 22179027 | — |
| Product | 6-Chloro2-(4-allyl-1-piperazinyl)-pyrazine hydrochloride | HCID 20396011 | — |
Reaction Steps
A stirred suspension of 6-chloro-2-(1-piperazinyl)-pyrazine hydrochloride (2.35 g, 10.0 mmol) and 2.8 g potassium carbonate in 25 ml of acetonitrile at 50° C. is treated with 0.9 ml (10.4 mmol) allylbromide. After 4 hours at 50° C. the mixture is concentrated under vacuum and the residue partitioned between water and chloroform. The chloroform extract is chromatographed on silica gel. Elution with 1% methanol-chloroform gives fractions containing 0.4 g (15%) title salt, mp 233.5°-234° C. by treatment with hydrogen chloride in ethanol-isopropanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04163849 |
| Source dataset | uspto-grants-1979_08 |
| ORD ID | ord-b94f9e1f61b3411887e43579950b58a4 |
| Source note | uspto-grants-1979_08 |