Table 2.
Synthesis of polyhydroquinoline derivatives by using MSN/C3N4/CNH catalyst under solvent free conditions.
| Entry | R | R′ | Yield (%) |
|---|---|---|---|
| 1 | C6H5 | Et | 94 |
| 2 | C6H5 | Me | 94 |
| 3 | 4-NO2C6H5 | Et | 96 |
| 4 | 4-NO2C6H5 | Me | 95 |
| 5 | 4-ClC6H5 | Et | 96 |
| 6 | 2-BrC6H5 | Et | 97 |
| 7 | 4-MeC6H5 | Et | 90 |
| 8 | 4-OHC6H5 | Et | 92 |
| 9 | 3-EtO-4-OHC6H5 | Et | 88 |
Reaction conditions: aldehyde (1 mmol), dimedone (1 mmol), ethyl acetoacetate (1 mmol), ammonium acetate (1.4 mmol), catalyst (10 mg) and reaction time (15 min).