HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butanedione → 7-Amino-8-chloro-2,3-dimethyl-quinoxaline-6-carboxylic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butanedione | HCID 650 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2,4,5-Triamino-3-chloro-benzoic acid methyl ester | HCID 57855994 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 7-Amino-8-chloro-2,3-dimethyl-quinoxaline-6-carboxylic acid methyl ester | HCID 57855919 | 62% |
Reaction Steps
To a solution of 1.5 g (6.96 mmol) of 2,4,5-triamino-3-chloro-benzoic acid methyl ester in 27 ml of EtOH, is added 0.81 ml (9.18 mmol) of 2,3-butanedione. The mixture is stirred under reflux during 1 hour. After cooling the mixture to ambient temperature EtOAc is added and the organic phase is washed with H2O (2 times). The organic phase is dried on Na2SO4, filtrated and evaporated. After purification by flash chromatography on silica gel, 1.18 g (4.22 mmol, 62%) of an orange-coloured solid were obtained. 1H-NMR (CDCl3, 300 MHz): ? ppm=2.67 (s, 3H), 2.75 (s, 3H), 3.97 (s, 3H), 6.47 (s br, 2H), 8.58 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08580785B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-1976bc22b6d7426abf9e944027ec306b |
| Source note | uspto-grants-2013_11 |