HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methylpiperazine → 2-Chloro-3-(4-methylpiperazin-1-YL)pyrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | 2,3-Dichloropyrazine | HCID 78575 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-Chloro-3-(4-methylpiperazin-1-YL)pyrazine | HCID 22036352 | 75% |
Reaction Steps
A mixture of 2,3-dichloropyrazine (10.1 g, 68 mmol) and N-methylpiperazine (10.15 g, 100 mmol) in acetonitrile (250 mL) was stirred at room temperature for 60 h. The solvent was removed under reduced pressure and the residue was taken up in CHCl3/brine. The dried (MgSO4) organic layer was concentrated and the remaining oil was purified by chromatography on silica gel using CHCl3/MeOH (95:5) as eluent to give 10.7 g (75%) of the title compound as an oil that crystallized upon standing: mp 34-36° C. Anal. (C9H13ClN4) C, H, N.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07534794B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-82c2c44ed4c64d36b80d7c03f72a40a5 |
| Source note | uspto-grants-2009_05 |