Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Butanedione | HCID 650 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Pyrosulfite | HCID 656671 | — |
| Reactant | Ethyl 2,3-diaminobenzoate | HCID 11171330 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 22037030 | HCID 22037030 | 67.2% |
Reaction Steps
2,3-Butanedione (0.0776 mol) was added at room temperature to a solution of sodium pyrosulfite (0.1 mol) in water (75 ml). The mixture was heated to 70° C. and then added to a solution of ethyl 2,3-diaminobenzoate (0.0776 mol) in water (75 ml). The mixture was stirred at 100° C. for 12 hours, cooled, basified with K2CO3 10% and =extracted with EtOAc. The organic layer was separated, dried (MgSO4), filtered and the solvent was evaporated. The residue (17.5 g) was purified by column chromatography over silica gel (eluent: CH2Cl2/EtOAc 93/7; 20–45 μm). The pure fractions were collected and the solvent was evaporated, yielding 12 g (67%) of ethyl 2,3-dimethyl-5-quinoxalinecarboxylate (interm. 6).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07071192B1 |
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| Source dataset | uspto-grants-2006_07 |
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| ORD ID | ord-a0f99a5dfa9a45848a8856bf58a18c6e |
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| Source note | uspto-grants-2006_07 |
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