Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Diethyl oxalacetate | HCID 66951 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 15224709 | HCID 15224709 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 12724759 | HCID 12724759 | 59% |
Reaction Steps
The procedure of Sircar, et al., (J. Med. Chem., 24:735-742 (1981)) was followed. A mixture of 5-amino-2-methylaminobenzoic acid hydrazide (35.05 g, 0.194 mol) and 95% diethyl oxalacetate, sodium salt (47.33 g, 0.214 mol, Aldrich Chemical Co.) in 1 L of water was refluxed for 2 hours. The dark solution was cooled to room temperature and sodium carbonate (22.68 g, 0.214 mol) was added. The solution was refluxed for 1 hour, then allowed to cool to room temperature overnight. A small amount of solid formed. The mixture was filtered through a pad of Celite, the filtrate was cooled and acidified by dropwise addition of 10% hydrochloric acid. At a pH of about 4, a solid formed, the mixture was filtered, and the yellow-green solid was washed with water and vacuum-dried to give 29.65 g (59%) of the title compound, mp 249°-252° C., dec.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05342942 |
|---|
| Source dataset | uspto-grants-1994_08 |
|---|
| ORD ID | ord-8e68d710e4574049942a9d692be322a8 |
|---|
| Source note | uspto-grants-1994_08 |
|---|