HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1399775Generated: October 31, 2026
Potassium Carbonate → 5,7-dichloro-3-{[2-methyl-3-(trifluoromethyl)phenyl]methyl}-3H-imidazo[4,5-b]pyridine
https://huagongshe.com/reaction/1399775
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(Bromomethyl)-2-methyl-3-(trifluoromethyl)benzene | HCID 2775617 | — |
| Reactant | 5,7-dichloro-1H-imidazo[4,5-b]pyridine | HCID 5949802 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5,7-dichloro-3-{[2-methyl-3-(trifluoromethyl)phenyl]methyl}-3H-imidazo[4,5-b]pyridine | HCID 89647778 | 47.6% |
Reaction Steps
Potassium carbonate (1139 mg, 8.24 mmol) was added to a solution of 5,7-dichloro-1H-imidazo[4,5-b]pyridine (500 mg, 2.66 mmol) in N,N-Dimethylformamide (DMF) (8.5 mL) and the mixture was stirred for 25 min. 1-(bromomethyl)-2-methyl-3-(trifluoromethyl)benzene (942 mg, 3.72 mmol) was then added and the reaction mixture was stirred at rt overnight. The mixture was partitioned between water and EtOAc. The aqueous layer was extracted with additional EtOAc (2×25 mL). The combined organic extracts were washed with brine, dried over Na2SO4 and evaporated. The residue was purified on silica gel (15 to 30% EtOAc in hexanes) to give 5,7-dichloro-3-{[2-methyl-3-(trifluoromethyl)phenyl]methyl}-3H-imidazo[4,5-b]pyridine (456 mg, 1.266 mmol, 47.6% yield) as an off-white powder. MS (ES+) m/e 359 (MH+) 1H NMR (400 MHz, DMSO-d6) δ ppm 8.64 (s, 1H), 7.68 (s, 1H), 7.66 (d, J=8.08 Hz, 1H), 7.33 (t, J=7.71 Hz, 1H), 7.07 (d, J=7.83 Hz, 1H), 5.62 (s, 2H) (Ar—CH3 hidden under DMSO peak).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08906910B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-475bdf12c56846fda3d7af4d64f0c520 |
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| Source note | uspto-grants-2014_12 |
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