HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-carbethoxycarbonylmethyl-quinoxalinium bromide → Ethyl imidazo[1,2-a]quinoxaline-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-carbethoxycarbonylmethyl-quinoxalinium bromide | HCID 20217059 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl imidazo[1,2-a]quinoxaline-2-carboxylate | HCID 13228325 | 88.1% |
Reaction Steps
A suspension of 0.4 g of the product of Step A in 15 ml of ethanol was refluxed for 2 hours and the resulting clear orange solution was concentrated to half its volume. The mixture was filtered to obtain 0.25 g of ethyl imidazo-[1,2-a]-quinoxaline-2-carboxylate as a pale yellow solid which were crystallized from an ether-methanol mixture to obtain the product in the form of soft-white needles melting at 184°-187° C. with decomposition.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04644002 |
| Source dataset | uspto-grants-1987_02 |
| ORD ID | ord-c28d37fa37cc449898444505ef17aa18 |
| Source note | uspto-grants-1987_02 |