HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802588Generated: November 3, 2026
8-Hydroxyquinoline → 4-hydroxymethyl-(2-fluoro-4-(2-oxopyridin-1(2H)-yl)phenyl)imidazole
https://huagongshe.com/reaction/1802588
Participants
| Role | Name | HCID | Charge |
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| Reactant | 8-Hydroxyquinoline | HCID 1923 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-iodo-2-fluoro-4-(2-oxopyridin-1(2H)-yl)benzene | HCID 59386661 | — |
| Reactant | HCID 178519868 | HCID 178519868 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 4-hydroxymethyl-(2-fluoro-4-(2-oxopyridin-1(2H)-yl)phenyl)imidazole | HCID 178516073 | — |
Reaction Steps
Alternatively as shown in Scheme 4,1-iodo-2-fluoro-4-(2-oxopyridin-1(2H)-yl)benzene 3-2 prepared as above, is treated with 4-hydroxymethylimidazole II-1 in the presence of 8-hydroxyquinoline, and K2CO3 in DMSO. The resulting mixture is degassed before being charged with CuI to give 4-hydroxymethyl-(2-fluoro-4-(2-oxopyridin-1(2H)-yl)phenyl)imidazole 4-1. The compound 4-1 is treated with thionyl chloride to give 4-chloromethyl-(2-fluoro-4-(2-oxopyridin-1(2H)-yl)phenyl)imidazole which is then treated with NaN3 to result in 4-azidomethyl-(2-fluoro-4-(2-oxopyridin-1(2H)-yl)phenyl)imidazole 4-2. The azide 4-2 is reduced with Ph3P to give 4-aminomethyl-(2-fluoro-4-(2-oxopyridin-1(2H)-yl)phenyl)imidazole 4-3. The compound 4-3 is then treated with 5-chlorothiophene-2-carboxylic acid 1-5 to give the title compound 21.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08349873B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-94f74c8e3bba410ab02007ac2ec43c76 |
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| Source note | uspto-grants-2013_01 |
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