HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromopyruvate → Ethyl 4-ethoxy-7,8-dichloroimidazo-[1,2-a]-quinoxaline-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromopyruvate | HCID 66144 | — |
| Reactant | 2-Amino-6,7-dichloro-3-ethoxy-quinoxaline | HCID 14067534 | — |
| Solvent | Isobutane | HCID 6360 | — |
| Product | Ethyl 4-ethoxy-7,8-dichloroimidazo-[1,2-a]-quinoxaline-2-carboxylate | HCID 14067535 | 10.9% |
Reaction Steps
A solution of 1 g of the product of Step A, 1 g of ethyl bromopyruvate and 50 ml of dimethylethane was stirred at room temperature for 5 days and the mixture was filtered to recover 0.51 g of a white crystalline solid. The latter was chromatographed over silica gel and was eluted with chloroform to obtain 0.15 g of ethyl 4-ethoxy-7,8-dichloroimidazo-[1,2-a]-quinoxaline-2-carboxylate in the form of a white crystalline solid melting at 256°-258° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04291033 |
| Source dataset | uspto-grants-1981_09 |
| ORD ID | ord-c9554f394b2d4ef79ff2f10aa7868e87 |
| Source note | uspto-grants-1981_09 |