HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572185Generated: November 2, 2026
Water → 9-(4-{[3-(2-Methoxyethyl)-3H-imidazo[4,5-b]pyridin-2-yl]oxy}phenyl)-9H-imidazo[1',2':1,2]imidazo[4,5-b]pyridine
https://huagongshe.com/reaction/572185
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-(2-methoxyethyl)-2-(methylsulfonyl)-3H-imidazo[4,5-b]pyridine | HCID 66727773 | — |
| Reactant | 4-(9H-imidazo[1',2':1,2]imidazo[4,5-b]pyridin-9-yl)phenol | HCID 86704986 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 9-(4-{[3-(2-Methoxyethyl)-3H-imidazo[4,5-b]pyridin-2-yl]oxy}phenyl)-9H-imidazo[1',2':1,2]imidazo[4,5-b]pyridine | HCID 60202407 | — |
Reaction Steps
To a solution of 4-(9H-imidazo[1′,2′:1,2]imidazo[4,5-b]pyridin-9-yl)phenol (175 mg) obtained in Example 9, step C) in DMF (2 ml) was added sodium hydride (60% in oil, 30 mg) at room temperature by small portions. After stirring for 10 min, a solution of 3-(2-methoxyethyl)-2-(methylsulfonyl)-3H-imidazo[4,5-b]pyridine[191 mg) in DMF (2 ml) was added, and the obtained mixture was stirred under microwave irradiation at 180° C. for 30 min. The reaction mixture was poured into water, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/THF) and recrystallized from ethanol to give the title compound (198 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09029388B2 |
|---|
| Source dataset | uspto-grants-2015_05 |
|---|
| ORD ID | ord-b567a040aca54573b1f99111a3dda01d |
|---|
| Source note | uspto-grants-2015_05 |
|---|