HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Dazoquinast
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl imidazo[1,2-a]quinoxaline-2-carboxylate | HCID 13228325 | — |
| Solvent | Water | HCID 962 | — |
| Product | Dazoquinast | HCID 71146 | 107.8% |
Reaction Steps
10 ml of 1N sodium hydroxide solution were added to a suspension of 0.63 g of ethyl imidazo-[1,2-a]-quinoxaline-2-carboxylate, 10 ml of ethanol and 30 ml of water and the mixture was refluxed for one hour. The ethanol was evaporated under reduced pressure from the resulting clear yellow solution and the aqueous phase was acidified with concentrated hydrochloric acid. The mixture was filtered to obtain 0.6 g of imidazo-[1,2-a]-quinoxaline-2-carboxylic acid in the form of a buff crystalline solid melting at 274°-275° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04644002 |
| Source dataset | uspto-grants-1987_02 |
| ORD ID | ord-e13a3de72d294beabe5c5d2727d101b0 |
| Source note | uspto-grants-1987_02 |