HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetaldehyde → 5-(Benzoxazol-2-yl)-2-methyl-1-tert-butoxycarbonylmethylbenzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Reactant | 2-(2-(Tert-butoxycarbonylmethylamino)anilin-5-yl)benzoxazole | HCID 67498333 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-(Benzoxazol-2-yl)-2-methyl-1-tert-butoxycarbonylmethylbenzimidazole | HCID 67497805 | 24% |
Reaction Steps
To a solution of 2-(2-(tert-butoxycarbonylmethylamino)anilin-5-yl)benzoxazole (see Working Example 91-1) (120 mg, 0.353 mmol) in dimethylformamide (2 mL) was added an aqueous solution of acetaldehyde (approx. 90%, 66 μL, 1.06 mmol) and oxone (217 mg, 0.353 mmol), and this was stirred at room temperature for 2 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 (30.7 mg, 24% yield) as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08829035B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-e19a6ef2df6b4adf929f599fe0a11e2c |
| Source note | uspto-grants-2014_09 |