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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 74281Generated: October 28, 2026

Acetic Anhydride → 5-(5-Acetylaminobenzoxazol-2-yl)-2-methyl-1-n-propylbenzimidazole

https://huagongshe.com/reaction/74281

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantHCID 67498866HCID 67498866—
SolventChloroformHCID 6212—
Product5-(5-Acetylaminobenzoxazol-2-yl)-2-methyl-1-n-propylbenzimidazoleHCID 6749769777.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829035B2
Source datasetuspto-grants-2014_09
ORD IDord-2002831dc48e4fa782897298ccbf5a57
Source noteuspto-grants-2014_09