Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 6-(Trifluoromethyl)imidazo[1,2-a]pyridine-2-carbaldehyde | HCID 71607228 | — |
| Reactant | HCID 178419651 | HCID 178419651 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66778779 | HCID 66778779 | 30% |
Reaction Steps
To a solution of 6-(trifluoromethyl)imidazo[1,2-a]pyridine-2-carbaldehyde (2.1 g) synthesized above in tetrahydrofuran (40 mL) was added dropwise cyclohexylmagnesium bromide (1M tetrahydrofuran solution, 15 mL) at 0° C. After stirring at 0° C. for 1 hr, aqueous ammonium chloride solution was added. The mixture was extracted with ethyl acetate, and the solvent was evaporated under reduced pressure. The precipitate was washed with ethanol-diisopropyl ether to give the title object compound (0.9 g, 30%) as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08436043B2 |
|---|
| Source dataset | uspto-grants-2013_05 |
|---|
| ORD ID | ord-4bbc383ff30149cf873d7d41b751cb98 |
|---|
| Source note | uspto-grants-2013_05 |
|---|