HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetaldehyde → 5-(Benzoxazol-2-yl)-1-(4-fluorophenyl)-2-methylbenzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Reactant | 2-(2-(4-Fluorophenyl)aminoanilin-5-yl)benzoxazole | HCID 67498132 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-(Benzoxazol-2-yl)-1-(4-fluorophenyl)-2-methylbenzimidazole | HCID 67498174 | 49% |
Reaction Steps
To a solution of 2-(2-(4-fluorophenyl)aminoanilin-5-yl)benzoxazole (see Working Example 34-1) (38.0 mg, 0.119 mmol) in dimethylformamide (2 mL) was added an aqueous solution of acetaldehyde (approx. 90%, 22.6 μL, 0.360 mmol) and oxone (73.2 mg, 0.119 mmol), and this was stirred at room temperature for 3 hours. After the reaction was complete, aqueous potassium carbonate solution was added, this was filtered and washed with water. The crystals obtained were purified by silica gel column chromatography to yield the title compound (20.0 mg, 49% yield) as light brown crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08829035B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-ba05cdd7cd0a4be1a10844316c68f610 |
| Source note | uspto-grants-2014_09 |