HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(Bromomethyl)benzophenone → HCID 11326145, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(Bromomethyl)benzophenone | HCID 122951 | — |
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | 2,6-Dimethyl-8-ethyl-1-deazapurine | HCID 9815374 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 11326145 | HCID 11326145 | 79.3% |
Reaction Steps
Commercially available 4-bromomethylbenzophenone (5.00 g, 18.2 mmol) was dissolved in DMF (100 mL), and 2-ethyl-5,7-dimethylimidazo[4,5-b]pyridine (3.82 g, 21.8 mmol) and lithium hydroxide monohydrate (0.920 g, 21.9 mmol) was added to the solution, followed by stirring at room temperature for 3 hours. After the reaction mixture was concentrated under reduced pressure, the residue was dissolved in ethyl acetate, and washed with water and saturated brine. The organic layer was dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=2:1), and recrystallized from ethanol to obtain Compound 1 (5.33 g, yield 79%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08507484B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-f1e0c04690434e9f8aff6fdc553f9469 |
| Source note | uspto-grants-2013_08 |