HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 6-Chloro-2-(4-cyclopropanecarbonyl-1-piperazinyl)-pyrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Cyclopropanecarbonyl chloride | HCID 77637 | — |
| Reactant | MK-212 hydrochloride | HCID 198421 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sodium Carbonate | HCID 10340 | — |
| Product | 6-Chloro-2-(4-cyclopropanecarbonyl-1-piperazinyl)-pyrazine | HCID 20396001 | 93.7% |
Reaction Steps
To a stirred suspension of 4.70 g (20.0 mmol) of 6-chloro-2-(1-piperazinyl)-pyrazine hydrochloride in 75 ml saturated aqueous sodium carbonate cooled in an ice bath is added 3 ml (33 mmol) of cyclopropanecarboxylic acid chloride. The mixture is stirred 45 minutes at ice bath temperature and then treated with 5 ml methylene chloride and warmed to room temperature during 30 minutes. Additional acid chloride (3 ml, 33 mmol) is added and stirring is continued 30 minutes longer. The mixture is diluted with water and extracted with chloroform to give 5 g crude 6-chloro-2-(4-cyclopropanecarbonyl-1-piperazinyl)-pyrazine which crystallizes, mp 69°-71° C. (100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04163849 |
| Source dataset | uspto-grants-1979_08 |
| ORD ID | ord-9c938ed1e24f40788e59c5891d546d37 |
| Source note | uspto-grants-1979_08 |