HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 86737689, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178486890 | HCID 178486890 | — |
| Product | HCID 86737689 | HCID 86737689 | — |
Reaction Steps
From 4,9-dihydro-6,7-dimethoxy-9-oxo-pyrazolo[5,1-b]-quinazoline-2-carboxylic acid (1.5 g; 5.2 mmole), anhydrous potassium carbonate (3.0 g; 22 mmole), methyl iodide (15 ml) and DMF (50 ml), following the procedure of Example 11, there is obtained 4,9-dihydro-6,7-dimethoxy-4-methyl-9-oxo-pyrazolo[5,1-b]quinazoline-2-carboxylic acid, methyl ester (1.8 g); mp 301°-303° (d). The crude methyl ester (1.8 g) is hydrolyzed with 1(N) sodium hydroxide solution (50 ml) as in Example 11 to give 4,9-dihydro-6,7-dimethoxy-4-methyl-9-oxo-pyrazolo-[5,1-b]quinazoline-2-carboxylic acid (0.95 g) mp 284°-5° (d), after crystallization from DMF/methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04261997 |
| Source dataset | uspto-grants-1981_04 |
| ORD ID | ord-cf861c2d9e1c4b4ea707148354819c2a |
| Source note | uspto-grants-1981_04 |