Synthesis of 5-functionalized thiophene aminoesters 3a–3l.
| ||
|---|---|---|
| Compound | R | Isolated yield (%) |
| 3a | 4-CO2Me–Ph– | 55 |
| 3b | 4-NO2–Ph– | 65 |
| 3c | 4-HO–Ph– | 64 |
| 3d | 3-Cl-4-F–Ph– | 82 |
| 3e | 4-Morpholinyl–Ph– | 73 |
| 3f | 4-(N-Methylpiperazinyl)–Ph– | 71 |
| 3g | 4-Piperidinyl–Ph– | 71 |
| 3h | 4-MeS–Ph– | 72 |
| 3i | 4-MeSO2–Ph– | 62 |
| 3j | 4-(H2N–SO2)–Ph– | 47 |
| 3k | 4-(Morpholinyl–SO2)–Ph– | 88 |
| 3l | 2-Chloropyrimidin-5-yl– | 44 |