Table 3.
Synthesis of 2-amino-4H- pyran derivates a
| |||||
|---|---|---|---|---|---|
| Entry | Product | Structure | Time (min) | M.P (OC) [Refs] | Yield b |
| 1 | 5a |
|
25 | 175–177 [40] | 96 |
| 2 | 5b |
|
35 | 173–175 [40] | 97 |
| 3 | 5c |
|
30 | 190 − 188 [40] | 98 |
| 4 | 5d |
|
30 | 132 − 130 [41] | 95 |
| 5 | 5e |
|
25 | 134 − 132 [40] | 96 |
| 6 | 5f |
|
40 | 192 − 188 [40] | 97 |
| 7 | 5 g |
|
25 | 136 − 134 [42] | 98 |
| 8 | 5 h |
|
30 | 192 − 190 [42] | 90 |
| 9 | 5i |
|
25 | 170 − 168 [43] | 96 |
| 10 | 6a |
|
25 | 229 − 227 [32] | 95 |
| 11 | 6b |
|
10 | 210 − 208 [31] | 90 |
| 12 | 6c |
|
30 | 191 − 189 [32] | 96 |
| 13 | 6d |
|
40 | 139 − 137 [32] | 88 |
| 14 | 6e |
|
25 | 120 − 118 [32] | 98 |
| 15 | 6f |
|
25 | 242 − 240 [32] | 94 |
| 16 | 6 g |
|
25 | 230 − 228 [44] | 96 |
a: Aldehydes (1 mmol), dimedone (1 mmol), and ethyl acetoacetate (1 mmol), in the presence of the L-Glu-MPS (20 mg) in EtOH (10 ml). b Isolated yield,