HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 5-(5-Acetylaminobenzoxazol-2-yl)-2-methyl-1-n-propylbenzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 67498866 | HCID 67498866 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 5-(5-Acetylaminobenzoxazol-2-yl)-2-methyl-1-n-propylbenzimidazole | HCID 67497697 | 77.4% |
Reaction Steps
To a solution of 5-(5-aminobenzoxazol-2-yl)-2-methyl-1-n-propylbenzimidazole (see Working Example 82-4) (200 mg, 0.653 mmol) in chloroform (5 mL) was added triethylamine (132 mg, 1.31 mmol) and acetic anhydride (100 mg, 0.979 mmol), and this was stirred at room temperature for 20 hours. After the reaction was complete, the solution was concentrated, the precipitated crystals were filtered, and after washing with water were dried to yield the title compound (176 mg, 77% yield) as pale yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08829035B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-2002831dc48e4fa782897298ccbf5a57 |
| Source note | uspto-grants-2014_09 |