HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 19808338, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 19808321 | HCID 19808321 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 19808338 | HCID 19808338 | 71.8% |
Reaction Steps
3-(8-Carboxy-1,4-dihydro-1-phenyl-[1]-benzothiopyrano[4,3-c]pyrazol-3-yl)-2-cyano-3-oxo-N-phenyl-propanamide (0.65 g) dissolved in dimethylformamide (50 ml) is reacted with methyl iodide (0.37 g) in the presence of anhydrous potassium carbonate (0.36 g) under stirring at room temperature for 2 hours. The reaction mixture is diluted with ice water and the precipitate is filtered, dissolved in chloroform and washed with 1N HCl and then with water. Evaporation of the solvent in vacuo gives a residue which is crystallized from CH2Cl2 /methanol to yield 0.48 g of 2-cyano-3-(1,4-dihydro-8-methoxycarbonyl-1-phenyl-[1]-benzothiopyrano[4,3-c]pyrazol-3-yl)-3-oxo-N-phenyl-propanamide, m.p. 228°-230° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05166152 |
| Source dataset | uspto-grants-1992_11 |
| ORD ID | ord-60db59c1c9de437aa9dd4ee65e170e92 |
| Source note | uspto-grants-1992_11 |