HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586374Generated: October 27, 2026
2-(3-fluorophenyl)-1H-imidazole → 6-chloro-2-{[2-(3-fluorophenyl)-1H-imidazol-1-yl]methyl}-3-propylimidazo[1,2-a]pyridine
https://huagongshe.com/reaction/586374
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(3-fluorophenyl)-1H-imidazole | HCID 316816 | — |
| Reactant | Dichloromethane methanol | HCID 21226129 | — |
| Reactant | 2-Chloromethyl-6-chloro-3-(1-propyl)-imidazolo[1,2-a]pyridine | HCID 22335107 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 6-chloro-2-{[2-(3-fluorophenyl)-1H-imidazol-1-yl]methyl}-3-propylimidazo[1,2-a]pyridine | HCID 22335084 | — |
Reaction Steps
Kt-BuO (0.69 mL of 1 M in THF, 0.69 mmol) is added to a solution of 3-fluoro-(1H-imidazol-2-yl)benzene (88 mg, 0.58 mmol) in anhydrous DMA (1 mL). After 15 minutes, 2-chloromethyl-6-chloro-3-(1-propyl)-imidazolo[1,2-a]pyridine (140 mg, 0.58 mmol) is added and the reaction mixture is stirred and heated at 60° C. for 15 minutes. The reaction mixture is diluted with EtOAc (10 mL), washed with water (3 mL), brine (3 mL), dried over Na2SO4, filtered and evaporated at reduced pressure to obtain a yellow solid. Sequential chromatography on silica gel eluting with EtOAc and then 5%MeOH/CH2Cl2 provides 6-chloro-2-{[2-(3-fluoropheny)-1H-imidazol-1-yl]methyl}-3-propylimidazo[1,2-a]pyridine as a cream-colored yellow solid. TLC (10% MeOH/CH2Cl2) Rf=0.35.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06936617B2 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-8d638e36cfbd4aaab052ecb27541dd34 |
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| Source note | uspto-grants-2005_08 |
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