Research Article
Ceric Ion Loaded MCM-41 Catalyzed Synthesis of Substituted Mono- and Bis-dihydropyrimidin-2(1H)-ones
Table 2
Ce-MCM-41 catalyzed synthesis of 3,4-dihydropyrimidinonesa.
| S. no. | | | | Product | Time (h) | Yield (%)b |
| 1 | H | Et | O | 4a | 1.0 | 94 | 2 | 4-OMe | Et | O | 4b | 1.5 | 90 | 3 | 4-Cl | Et | O | 4c | 1.0 | 93 | 4 | 4-NO2 | Et | O | 4d | 1.5 | 89 | 5 | 4-OH | Et | O | 4e | 1.5 | 88 | 6 | 2-OH | Et | O | 4f | 2.0 | 87 | 7 | 2-Cl | Et | O | 4g | 1.5 | 84 | 8 | 3-NO2 | Et | O | 4h | 2.0 | 86 | 9 | 2-NO2 | Et | O | 4i | 1.0 | 81 | 10 | H | Me | O | 4j | 1.0 | 93 | 11 | 4-Cl | Me | O | 4k | 1.0 | 90 | 12 | 4-NO2 | Me | O | 4l | 1.5 | 87 | 13 | 3-NO2 | Me | O | 4m | 2.0 | 85 | 14 | 2-OH | Me | O | 4n | 1.5 | 83 | 15 | 4-OCH3 | Me | O | 4o | 2.0 | 89 | 16 | H | Et | S | 4p | 1.0 | 89 | 17 | 4-Cl | Et | S | 4q | 1.5 | 91 | 18 | 4-NO2 | Et | S | 4r | 1.5 | 86 | 19 | 3-NO2 | Et | S | 4s | 1.5 | 84 | 20 | H | Me | S | 4t | 1.0 | 90 | 21 | 4-Cl | Me | S | 4u | 1.0 | 91 | 22 | 4-NO2 | Me | S | 4v | 1.5 | 87 |
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Ce-MCM-41 catalyzed Biginelli reaction under solvent-free conditions.
bIsolated yields.
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