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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1162465Generated: October 28, 2026

Pyridine → N-(6-bromo-1H-benzimidazol-2-yl)acetamide

https://huagongshe.com/reaction/1162465

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
Reactant5-Bromo-1H-1,3-benzodiazol-2-amineHCID 20430861—
SolventDichloromethaneHCID 6344—
ProductN-(6-bromo-1H-benzimidazol-2-yl)acetamideHCID 1105418928%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a 250 mL round-bottomed flask was added 6-bromo-1H-benzo[d]imidazol-2-amine (2.00 g, 9.43 mmol, Carbocore, The Woodlands, Tex.), DCM (100 mL), pyridine (1.0 mL, 12.3 mmol) and acetic anhydride (0.979 mL, 10.4 mmol). The mixture was stirred at 25° C. for 18 h. The solution was concentrated and then diluted with 10% MeOH (2M in NH3)/CH2Cl2 until homogeneous and then the solution was concentrated onto silica. Purification by silica gel chromatography (0.5 to 5.0% MeOH (2 M in NH3)/CH2Cl2) afforded the title compound as a white solid (0.676 g, 28%). MS (ESI, positive ion) m/z: 254 (M(79Br)+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820665B2
Source datasetuspto-grants-2010_10
ORD IDord-a1c288058d56440d9fbf8b6f44e53b9b
Source noteuspto-grants-2010_10