Table 2.
Synthesis of 1,4-dihydropyridine derivatives using g-C3N4@l-arginine nanocatalyst.
| Entry | R | Product | Time (min) | Mp (°C) | Mp (°C, ref.) | Yield (%) |
|---|---|---|---|---|---|---|
| 1 | H | 5a | 10 | 217–219 | 218–220 17 | 95 |
| 2 | 4-Cl | 5b | 15 | 240–242 | 241–243 17 | 94 |
| 3 | 4-OH | 5c | 20 | 230–232 | 231–232 14 | 89 |
| 4 | 4-NO2 | 5d | 15 | 239–241 | 240–242 14 | 90 |
| 5 | 4-Me | 5e | 25 | 254–256 | 250 32 | 87 |
Reaction conditions: benzaldehyde (1 mmol), ethyl acetoacetate (1 mmol), dimedone (1 mmol), and ammonium acetate (1 mmol), g-C3N4@l-arginine (20 mg) and ethanol (7 mL) under reflux conditions.