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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 5-Bromo-1H-1,3-benzodiazol-2-amine | HCID 20430861 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(6-bromo-1H-benzimidazol-2-yl)acetamide | HCID 11054189 | 28% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07820665B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-a1c288058d56440d9fbf8b6f44e53b9b |
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| Source note | uspto-grants-2010_10 |
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