HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 4,5-dihydro-4-oxoimidazo-[1,2-a]-quinoxaline-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 2-Amino-1-carbethoxycarbonylmethyl-3-chloroquinoxalinium bromide | HCID 14067523 | — |
| Product | Ethyl 4,5-dihydro-4-oxoimidazo-[1,2-a]-quinoxaline-2-carboxylate | HCID 13770479 | — |
Reaction Steps
A suspension of 6.5 g of the product of Step A in 500 ml of ethanol was refluxed with stirring for 2 hours and the resulting clear yellow solution was concentrated and cooled in a refrigerator. The mixture was filtered and then 3.70 g of white crystalline product was crystallized from ethanol to obtain ethyl 4,5-dihydro-4-oxoimidazo-[1,2-a]-quinoxaline-2-carboxylate in the form of shiny crystals melting at 292°-293° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04291033 |
| Source dataset | uspto-grants-1981_09 |
| ORD ID | ord-5f8decd4314c4126852b17f6599f5377 |
| Source note | uspto-grants-1981_09 |