HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorosuccinimide → HCID 22036518, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | 2-Chloro-3-(piperazin-1-yl)pyrazine | HCID 14086438 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 22036518 | HCID 22036518 | 45% |
Reaction Steps
To a suspension of 2-chloro-3-(1-piperazinyl)pyrazine (11.7 g, 58.7 mmol; from Example 90, Step 1) in CHCl3 (50 mL) was N-chlorosuccinimid (14.4 g, 108 mmol) added and the mixture was heated at reflux for 30 minutes. The reaction mixture was cooled to ambient temperature and extracted twice with water. The combined aqueous phases were made alkaline (11 M NaOH), saturated with NaCl, cooled, and extracted with EtOAc (×3). Concentration of the combined, dried (MgSO4), organic phases afforded 6.12 g (45%) of the title compound as a brown oil which crystallized upon standing: mp 89-97° C. Anal. (C8H10Cl2N4.⅓H2O) C, H, N.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07534794B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-19f62aaf4e994ed2b1c45060de9c0c3c |
| Source note | uspto-grants-2009_05 |