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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922763Generated: November 2, 2026

Diisopropylethylamine → 4-(4-Fluorophenyl)-7-[(4-formyl-1H-pyrazol-1-yl)methyl]-2-quinolinecarbonitrile

https://huagongshe.com/reaction/922763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1H-pyrazole-4-carbaldehydeHCID 5130673—
Reactant7-(Bromomethyl)-4-(4-fluorophenyl)quinoline-2-carbonitrileHCID 19427011—
SolventAcetonitrileHCID 6342—
Product4-(4-Fluorophenyl)-7-[(4-formyl-1H-pyrazol-1-yl)methyl]-2-quinolinecarbonitrileHCID 8954374852.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278960B2
Source datasetuspto-grants-2016_03
ORD IDord-a46d787f7afd4bcf8064fef62079f549
Source noteuspto-grants-2016_03