Table 3. Calculated Lipophilic Character log P of the Synthesized Compounds.
| compd no. | Y | Ar | Ar1 | log Pa |
|---|---|---|---|---|
| 3a | − | Ph | − | 2.06 |
| 3b | − | 4-Me-Ph | − | 2.50 |
| 5a | NH2 | Ph | − | 3.27 |
| 5b | NH2 | 4-Me-Ph | − | 3.72 |
| 5c | OH | Ph | − | 3.57 |
| 5d | OH | 4-Me-Ph | − | 4.02 |
| 9a | NH2 | Ph | Ph | 4.41 |
| 9b | NH2 | 4-Me-Ph | Ph | 4.86 |
| 9c | NH2 | Ph | 4-Me-Ph | 4.86 |
| 9d | NH2 | 4-Me-Ph | 4-Me-Ph | 5.30 |
| 9e | NH2 | Ph | 4-MeO-Ph | 4.46 |
| 9f | NH2 | 4-Me-Ph | 4-MeO-Ph | 4.91 |
| 11a | NH2 | Ph | − | 2.43 |
| 11b | NH2 | 4-Me-Ph | − | 2.87 |
| SD | –0.04 |
Calculations were performed using Molinspiration online property calculation toolkit (http://www.molinspiration.com). log P: logarithm of compound partition coefficient between n-octanol and water.
