HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 613489Generated: October 26, 2026
Imidazole → 8-(2,6-Dichlorobenzoylamino)-3-(imidazol-1-ylmethyl)quinoline
https://huagongshe.com/reaction/613489
Participants
| Role | Name | HCID | Charge |
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| Reactant | Imidazole | HCID 795 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2,2'-Azobis(2,4-dimethyl-4-methoxyvaleronitrile) | HCID 85867 | — |
| Reactant | 3-Bromomethyl-8-(2,6-dichlorobenzoylamino)quinoline | HCID 19592388 | — |
| Reactant | 8-(2,6-Dichlorobenzoylamino)-3-methylquinoline | HCID 19592707 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 8-(2,6-Dichlorobenzoylamino)-3-(imidazol-1-ylmethyl)quinoline | HCID 19592660 | — |
Reaction Steps
A mixture of 8-(2,6-dichlorobenzoylamino)-3-methylquinoline (104 mg), N-bromosuccinimide (67.1 mg) and 2,2'-azobis(2,4-dimethyl-4-methoxyvaleronitrile) (20.1 mg) in carbon tetrachloride (3 ml) was refluxed for 2 hours. After cooling, the mixture was washed with water, saturated sodium bicarbonate solution and brine, dried over magnesium sulfate and evaporated in vacuo to give a residue containing 3-bromomethyl-8-(2,6-dichlorobenzoylamino)quinoline. The residue was dissolved in ethylene chloride, and imidazole (64.1 mg) was added thereto. After stirring for 2.5 hours at 60° C., the mixture was washed with water and brine, dried over magnesium sulfate and evaporated in vacuo. The residue was purified by column chromatography on silica gel (ethyl acetate-dichloromethane) to give 8-(2,6-dichlorobenzoylamino)-3-(imidazol-1-ylmethyl)quinoline (36.2 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06008230 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-08c53389d8a24d998fde806acea60354 |
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| Source note | uspto-grants-1999_12 |
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