HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitrobenzamidine hydrochloride → 6-Hydroxy-5-methoxy-2-(4-nitro-phenyl)-3H-pyrimidin-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitrobenzamidine hydrochloride | HCID 170625 | — |
| Reactant | 2-Methoxypropandioic acid ethyl methyl ester | HCID 57351026 | — |
| Reactant | HCID 178418582 | HCID 178418582 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 6-Hydroxy-5-methoxy-2-(4-nitro-phenyl)-3H-pyrimidin-4-one | HCID 67295444 | 65% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
The NaOCH3 (7.8 g, 3 eq) was added to a stirred solution of 1-ethyl 3-methyl 2-methoxymalonate (11 g, 1.3 eq), 4-nitrobenzimidamide hydrochloride (9.6 g, 1 eq) and EtOH (240 ml) and the mixture was refluxed for 8 hrs. After 8 hrs, the solvent was evaporated and water (10˜15 ml) was added to the mixture then the mixture was cooled to 0° C. and carefully acidified with conc. HCl. After overnight cooling, it led to the formation of brown precipitates. The mixture was filtered and the precipitates was dried in vacuo to give a brown solid (65%) as a product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09315491B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-89b00234122243398bfec657cbefe635 |
| Source note | uspto-grants-2016_04 |