HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 5-[(Imidazo[1,2-A]pyridin-8-Yl)methoxy]-2-Methoxypyridine-4-Carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 8-(Chloromethyl)imidazo[1,2-a]pyridine | HCID 21661582 | — |
| Reactant | 5-Hydroxy-2-methoxyisonicotinaldehyde | HCID 72212498 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-[(Imidazo[1,2-A]pyridin-8-Yl)methoxy]-2-Methoxypyridine-4-Carbaldehyde | HCID 71620811 | 38% |
Reaction Conditions
| Temperature | 125 °C |
|---|
Reaction Steps
A mixture of 5-hydroxy-2-methoxyisonicotinaldehyde (723.6 mg, 4.7 mmol), 8-(chloromethyl)-imidazol[1,2-a]pyridine (785 mg, 4.7 mmol), and K2CO3 (1.9 g, 14.1 mmol) in DMF (20 mL) was heated at microwave reactor at 125° C. for 15 min. The mixture was filtered and concentrated. The residue was purified on silica gel (50-100% EtOAc in hexanes) to give 5-(imidazo[1,2-a]pyridin-8-ylmethoxy)-2-methoxyisonicotinaldehyde (500 mg, 38%) as an off-white solid. 1H NMR (400 MHz; DMSO) δ=10.37 (s, 1H), 8.58 (d, 1H), 8.39 (s, 1H), 8.02 (s, 1H), 7.61 (s, 1H), 7.44 (d, 1H), 6.98 (s, 1H), 6.93 (t, 1H), 5.61 (s, 2H), 3.84 (s, 3H). LRMS (M+H+) m/z 284.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09012450B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-b99d7cf281554e0bb8e207f23bd5fa6f |
| Source note | uspto-grants-2015_04 |