Table 4.
Entry | R1 | R2 | Yield (%) 2 |
---|---|---|---|
1 | 4-Me-Ph | Et | 86 |
2 | Ph | Et | 61 |
3 | 4-Br-Ph | Et | 46 |
4 | 4-CF3-Ph | Et | 64 |
5 | 2-OMe-Ph | Et | 55 |
6 | 2-NaPh | Et | 60 |
7 | 2-Cl,3-Cl-Ph | Et | 42 |
8 | (3-OMe,4-OMe,5-OMe)-Ph | Et | 37 |
9 | Et | 64 | |
10 | CH2CH2-Ph | Et | 45 |
11 | Me | Et | 80 |
12 | Pr | Et | 74 |
13 | CH2tBu | Et | 71 |
14 | Et | 77 | |
15 | 4-Me-Ph | Me | 65 |
1 Reaction conditions: 4-aminoindole/aldehyde/alkyne = 1.5:1:1.5, LSA-FAS-Cu2+ (20 mol%), EtOH (1 mL), 60 °C, 7 h. 2 Isolated yield.