HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-Dichloroquinoxaline → 2-benzyl-3-chloroquinoxaline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-Dichloroquinoxaline | HCID 16659 | — |
| Reactant | HCID 57590379 | HCID 57590379 | — |
| Reactant | HCID 178418336 | HCID 178418336 | — |
| Reactant | HCID 178509214 | HCID 178509214 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-benzyl-3-chloroquinoxaline | HCID 488811 | — |
Reaction Steps
Intermediate 3 can be prepared from the starting material 2,3-dichloroquinoxaline 1 following the reaction in Scheme 1. In this manner, quinoxaline 1 can be reacted with benzylmagnesium chloride in THF to afford 2-benzyl-3-chloroquinoxaline 2. 2-Benzylquinoxalines can also be prepared by reaction with alternative alkylating reagents, such as, but not limited to, benzyllithium. 2-Benzyl-3-chloroquinoxaline 2 can be reacted with cyanide to obtain intermediate 2-benzyl-3-cyanoquinoxaline 3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07501416B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-39b98bd20bf342e696ee6a5bad97b8d0 |
| Source note | uspto-grants-2009_03 |