HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 10560736, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,3-Dichloroquinoxaline | HCID 16659 | — |
| Reactant | Propargylamine | HCID 239041 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 10560736 | HCID 10560736 | — |
Reaction Steps
A mixture of 10 g of 2,3-dichloroquinoxaline, 4.5 ml of propargylamine, 10.5 ml of triethylamine in 50 ml of ethanol is refluxed for 4 h. After evaporating under vacuum the resulting mixture, the residue is chromatographed on SiO2 (eluent: CH2Cl2) thereby obtaining 7.0 g of 2-chloro-3-(propargylamino)quinoxaline (IR (KBr): 3441, 3282, 1518 cm-1). This product is then added with 10 ml of concentrated sulphuric acid and the resulting mixture is stirred at 90° C. for 1 h. After cooling down and cautiously neutralizing with aqueous NaOH, the resulting precipitate is filtered under vacuum, washed, dried, decolorized and recrystallized from dimethylformamide, thereby obtaining 2.4 g of 1-methylimidazo[1,2-a]quinoxaline-4(5H)-one (m.p. >300° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06124287 |
| Source dataset | uspto-grants-2000_09 |
| ORD ID | ord-72b6dfe5bc6c4e07ac6106d26e528101 |
| Source note | uspto-grants-2000_09 |