HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Diethyl 2-oxopropanedioate → ethyl 3,4-dihydro-7-[1-(1H-imidazol-1-yl)-2-methylpropyl]3-oxo-2-quinoxalinecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Diethyl 2-oxopropanedioate | HCID 69105 | — |
| Reactant | 4-[1-(1H-imidazol-1-yl)-2-methylpropyl]-1,2-benzenediamine | HCID 14518426 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | ethyl 3,4-dihydro-7-[1-(1H-imidazol-1-yl)-2-methylpropyl]3-oxo-2-quinoxalinecarboxylate | HCID 19875876 | 14% |
Reaction Steps
A solution of 15 parts of 4-[1-(1H-imidazol-1-yl)-2-methylpropyl]-1,2-benzenediamine and 12.5 parts of diethyl 2-oxo-1,3-propanedioate in 80 parts of ethanol was stirred for 2 hours at reflux temperature. The reaction mixture was evaporated and the residue was purified by column chromatography over silica gel using a mixture of dichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from a mixture of acetonitrile and ethanol. The product was filtered off and dried, yielding 3.1 parts (14.0%) of ethyl 3,4-dihydro-7-[1-(1H-imidazol-1-yl)-2-methylpropyl]-3-oxo-2-quinoxalinecarboxylate; mp. 229.7° C. (comp. 107).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05028606 |
| Source dataset | uspto-grants-1991_07 |
| ORD ID | ord-ca710a691f064426b163012343375a21 |
| Source note | uspto-grants-1991_07 |