HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 4-(4-Fluorophenyl)-7-[(4-formyl-1H-pyrazol-1-yl)methyl]-2-quinolinecarbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1H-pyrazole-4-carbaldehyde | HCID 5130673 | — |
| Reactant | 7-(Bromomethyl)-4-(4-fluorophenyl)quinoline-2-carbonitrile | HCID 19427011 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-(4-Fluorophenyl)-7-[(4-formyl-1H-pyrazol-1-yl)methyl]-2-quinolinecarbonitrile | HCID 89543748 | 52.7% |
Reaction Steps
7-(Bromomethyl)-4-(4-fluorophenyl)quinoline-2-carbonitrile (2-1, 100.0 mg, 0.293 mmol, 1.0 equiv.), DIEA (0.051 ml, 0.293 mmol, 1.0 equiv.), and 1-H-pyrazole-4-carbaldehyde (33.8 mg, 0.352 mmol, 1.2 equiv.) were added to acetonitrile (1.0 mL) in a microwave reaction vessel and the resulting mixture was irradiated with microwave at 180° C. for 30 minutes. The reaction mixture was cooled and concentrated and the residue was purified by reverse phase HPLC (H2O/CH3CN gradient w/0.1% TFA modifier) to afford 4-(4-fluorophenyl)-7-[(4-formyl-1H-pyrazol-1-yl)methyl]quinoline-2-carbonitrile (3-8, 55.0 mg, 52.7%) as a colorless solid. LRMS m/z (M+H)+ 357.1 found, 357.1 required.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09278960B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-a46d787f7afd4bcf8064fef62079f549 |
| Source note | uspto-grants-2016_03 |