HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-4-bromopyridine-3-carbonitrile → 7-Bromo-3-(2,2,2-trifluoro-ethyl)-imidazo[1,2-a]pyridine-8-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-4-bromopyridine-3-carbonitrile | HCID 58081121 | — |
| Reactant | 2-Bromo-4,4,4-trifluorobutyraldehyde | HCID 58081140 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 7-Bromo-3-(2,2,2-trifluoro-ethyl)-imidazo[1,2-a]pyridine-8-carbonitrile | HCID 58081128 | 48.8% |
Reaction Conditions
| Temperature | 150 °C |
|---|
Reaction Steps
A mixture of compounds D8 (2 g, 10.1 mmol) and D4 (2.898 g, 14.14 mmol) in EtOH (10 ml) was subjected to microwave heating at 150° C. for 40 min. After cooling to room temperature, the solvent was evaporated in vacuo. The residue thus obtained was diluted with EtOAc and washed with water. The organic layer was separated and washed with water, then with 1M HCl (aqueous solution), dried (MgSO4) and evaporated in vacuo. The crude product thus obtained was triturated with diethylether to yield compound D9 (1.5 g, 48.8%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08691813B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-4f1da4511e3c44189c88ec8c78263079 |
| Source note | uspto-grants-2014_04 |