HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine → 2-Hydrazino-6,7-difluoroquinoxaline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | 2-Chloro-6,7-difluoroquinoxaline | HCID 10375543 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Hydrazino-6,7-difluoroquinoxaline | HCID 10262078 | — |
Reaction Steps
The foregoing methodology was followed starting with 2-chloro-6,7-difluoroquinoxaline. This compound (4.00 g, 19.9 mmol) was dissolved in 100 ml of absolute EtOH. Hydrazine (1.4 ml, 44 mmol) was added, and the mixture heated at reflux for 21/2 hours. The mixture was cooled and allowed to stand overnight before collecting the resulting precipitate, yielding 3.80 g of an orange, solid 2-hydrazino-6,7-difluoroquinoxaline. This product (3.8 g, 19.4 mmol) was stirred in 30 ml triethylorthoformate and heated at reflux (100° C.) for 5 hours. The resulting product was cooled to room temperature, filtered and dried, yielding 2.63 g of 7,8-difluoro-1,2,4-triazolo[4,3-a]quinoxaline (13).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05153196 |
| Source dataset | uspto-grants-1992_10 |
| ORD ID | ord-4963c06800064116a582bfabb452beb8 |
| Source note | uspto-grants-1992_10 |