HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 4-(Benzyloxy)-6-(6-(2,6-difluorophenyl)pyridin-2-yl)quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2,6-Difluorophenylboronic acid | HCID 2734336 | — |
| Reactant | 4-(Benzyloxy)-6-(6-bromopyridin-2-yl)quinoline | HCID 58387598 | — |
| Solvent | Toluene ethanol | HCID 21863594 | — |
| Product | 4-(Benzyloxy)-6-(6-(2,6-difluorophenyl)pyridin-2-yl)quinoline | HCID 58387567 | 74% |
Reaction Steps
A solution of 4-(benzyloxy)-6-(6-bromopyridin-2-yl)quinoline (1.0 equiv.), 2,6 difluorophenylboronic acid (3.0 equiv.), diisopropylethylamine (3.0 equiv) and tetrakis(triphenylphospine)palladium (0.1 equiv.) in 1:1 toluene/ethanol was heated in a microwave at 120° C. for 20 minutes. Upon cooling, the solution was partitioned between EtOAc and H2O. Upon separation, the organic layer was washed with NaCl(sat.), dried over MgSO4, concentrated and purified by silica gel chromatography (60-75 EtOAc/hexanes eluant) to yield 4-(benzyloxy)-6-(6-(2,6-difluorophenyl)pyridin-2-yl)quinoline (74%). LC/MS=425.1 (M+H), LC=3.59 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08735424B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-240face549054277bf8b01839b413245 |
| Source note | uspto-grants-2014_05 |