HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2246436Generated: November 1, 2026
Potassium Carbonate → 2-dimethylamino-6-(4-ethoxy-3-trifluoromethyl-phenyl)-1H-imidazo[4,5-c]pyridine-4-carbonitrile
https://huagongshe.com/reaction/2246436
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Ethoxy-3-(trifluoromethyl)benzeneboronic acid | HCID 44558184 | — |
| Reactant | 6-chloro-2-dimethylamino-1H-imidazo[4,5-c]pyridine-4-carbonitrile | HCID 58938132 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-dimethylamino-6-(4-ethoxy-3-trifluoromethyl-phenyl)-1H-imidazo[4,5-c]pyridine-4-carbonitrile | HCID 58938123 | 3% |
Reaction Steps
A suspension of 6-chloro-2-dimethylamino-1H-imidazo[4,5-c]pyridine-4-carbonitrile (100 mg, 0.45 mmol), 4-ethoxy-3-trifluoromethyl-phenyl boronic acid (198 mg, 0.88 mmol) tetrakis(triphenylphosphine)palladium(0) (50 mg, ˜10 mol %) and potassium carbonate (193.0 mg, 1.39 mmol) in THF (3 ml) was heated to 130° C. for 6 minutes in the “Smith” microwave. The crude mixture was concentrated under reduced pressure to remove THF before partitioning between ethyl acetate and water. The organic layer was separated, dried over sodium sulfate and concentrated under reduced pressure. The material was then dissolved in DMSO and purified in aliquots by preparative HPLC. The desired fractions were collected and concentrated to give a white solid which was washed with ether to afford 2-dimethylamino-6-(4-ethoxy-3-trifluoromethyl-phenyl)-1H-imidazo[4,5-c]pyridine-4-carbonitrile (5.0 mg)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07687515B2 |
|---|
| Source dataset | uspto-grants-2010_03 |
|---|
| ORD ID | ord-102f7f63ac584b16ad4ba8611f9f5416 |
|---|
| Source note | uspto-grants-2010_03 |
|---|