HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → 2-cyano-3-(5-ethoxycarbonyl-1,4-dihydro-1-phenyl-indeno[1,2-c]pyrazol-3-yl)-3-oxo-N-phenyl-propanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-(5-Carboxy-1,4-dihydro-1-phenyl-indeno[1,2-c]pyrazol-3-yl)-2-cyano-3-oxo-N-phenyl-propanamide | HCID 19932560 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-cyano-3-(5-ethoxycarbonyl-1,4-dihydro-1-phenyl-indeno[1,2-c]pyrazol-3-yl)-3-oxo-N-phenyl-propanamide | HCID 19932621 | 77.9% |
Reaction Steps
3-(5-Carboxy-1,4-dihydro-1-phenyl-indeno[1,2-c]pyrazol-3-yl)-2-cyano-3-oxo-N-phenyl-propanamide (2.3 g) dissolved in dimethylformamide (25 ml) is reacted with ethyl iodide (1.55 g) in the presence of anhydrous potassium carbonate (1.4 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 1.9 g of 2-cyano-3-(5-ethoxycarbonyl-1,4-dihydro -1-phenyl-indeno[1,2-c]pyrazol-3-yl)-3-oxo-N-phenyl-propanamide, m.p. 233°-236° C. dec.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05424308 |
| Source dataset | uspto-grants-1995_06 |
| ORD ID | ord-0636a6b1d2a1493ba8579365dde00317 |
| Source note | uspto-grants-1995_06 |