Table 2.
One-pot reaction for the synthesis of compound 7.
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| entry | Ar1 | Ar2 | R1 | product | yield (%)b |
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| 1 | 2-thiophenyl | 3-OMe-4-FC6H3 | CO2Et | 7a | 66 |
| 2 | 2-thiophenyl | 2-furanyl | CO2Et | 7b | 51 |
| 3 | 2-thiophenyl | 3-pyridinyl | CO2Et | 7c | 43 |
| 4 | 2-FC6H4 | 4-ClC6H4 | CO2Et | 7d | 72 |
| 5 | 4-BrC6H4 | 4-ClC6H4 | CO2Et | 7e | 66 |
| 6 | 4-BrC6H4 | Ph | COMe | 7f | trace |
| 7 | 4-BrC6H4 | Ph | Ph | 7g | – |
| 8 | 4-BrC6H4 | CO2Et | CO2Et | 7h | messy |
| 9 | 4-BrC6H4 | ethyl | CO2Et | 7i | messy |
aIsolated yield. Reaction conditions are same as Table 1, entry 5.