HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262744Generated: October 25, 2026
Formic Acid → N-{1-[1-(3-Bromo-phenyl)-1H-benzoimidazol-5-yl]-ethyl}-formamide
https://huagongshe.com/reaction/2262744
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Formamide | HCID 713 | — |
| Reactant | 1-(1-(3-bromophenyl)-1H-benzo[d]imidazol-5-yl)ethanone | HCID 54030307 | — |
| Product | N-{1-[1-(3-Bromo-phenyl)-1H-benzoimidazol-5-yl]-ethyl}-formamide | HCID 57572242 | 60% |
Reaction Steps
A mixture of 1-[1-(3-bromo-phenyl)-1H-benzoimidazol-5-yl]-ethanone (7.5 g, 23.8 mmol), formamide (9.5 ml, 23.8 mmol) and formic acid (22.4 ml, 595 mmol) was stirred at 190° C. for 7 hours. The cooled mixture was decanted. The residue was rendered alkaline by addition of saturated, aqueous sodium carbonate and extracted with ethyl acetate. The organic extract was dried over magnesium sulphate and concentrated in vacuo. The concentrate was eluted through silica gel with a mixture of dichloromethane, methanol and aqueous ammonia (9:1:0.1 v/v/v) to afford the desired product (60%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07851490B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-f780767cce164e6fad9c10d0134034ce |
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| Source note | uspto-grants-2010_12 |
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