HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 4-oxo-10-(2-ethylbutyramido)-4H-pyrimido[1,2-C]quinazoline-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Lithium iodide | HCID 66321 | — |
| Reactant | methyl 4-oxo-10-(2-ethylbutyramido)-4H-pyrimido[1,2-C]quinazoline-3-carboxylate | HCID 13060555 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-oxo-10-(2-ethylbutyramido)-4H-pyrimido[1,2-C]quinazoline-3-carboxylic acid | HCID 13060559 | 22.7% |
Reaction Conditions
| Temperature | 120 °C |
|---|
Reaction Steps
A mixture of methyl 4-oxo-10-(2-ethylbutyramido)-4H-pyrmido[1,2-C]quinazoline-3-carboxylate (3.2 g), anhydrous lithium iodide (8.0 g) and dry pyridine (32 ml) was stirred at 120° C. for 1.5 hours. The reaction mixture was concentrated under reduced pressure to give a residue, which was dissolved in water. Insoluble materials were removed by filtration. The aqueous layer was adjusted to pH 1-2 with conc. hydrochloric acid to give crystals, which were separated by filtration and dried. The crude crystals were washed with methanol three times and recrystallized from acetonitrile to give 4-oxo-10-(2-ethylbutyramido)-4H-pyrimido[1,2-C]quinazoline-3-carboxylic acid (0.7 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04543356 |
| Source dataset | uspto-grants-1985_09 |
| ORD ID | ord-ec6bc8db607644849617683f7e835ccc |
| Source note | uspto-grants-1985_09 |