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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720415Generated: October 26, 2026

Imidazole → 3-Cyano-1-(4-imidazol-1-yl-benzoyl)-pyrrolo[1,2-a]quinoline

https://huagongshe.com/reaction/720415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantCarbonate IonHCID 19660—
Reactant3-Cyano (4-fluoro-benzoyl)-pyrrolo[1,2-a]quinolineHCID 10267630—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product3-Cyano-1-(4-imidazol-1-yl-benzoyl)-pyrrolo[1,2-a]quinolineHCID 2189210676.2%

Reaction Steps

A mixture of 3-cyano-(4-fluoro-benzoyl)-pyrrolo[1,2-a]quinoline (8 mg, 0.025 mmol), pottasium carbonate (10 mg, 0.072 mmol) and imidazole (5 mg, 0.073 mmol) were heated in 500 μL of DMF overnight. The reaction mixture was cooled to room temperature, diluted with 10 mL of ethyl acetate, washed with water (3×10 mL), saturated NaCl and the organic layer was dried over anhydrous Na2SO4, filtered and evaporated. The crude was purified by chromatography (3% methanol/chloroform) to yield the title compound (6.9 mg, 75%). 1H NMR (CDCl3): 8.21 (dt, J=7.80, 1.20 Hz, 2H), 8.08 (d, J=8.72 Hz, 1H), 8.02 (s, 1H), 7.87 (dd, J=7.81, 1.82 Hz, 1H), 7.73 (m, 2H), 7.60 (m, 4H), 7.46 (s, 1H), 7.42 (t, J=1.24 Hz, 1H), 7.30 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135480B2
Source datasetuspto-grants-2006_11
ORD IDord-107b03b101804228b89eaed877375598
Source noteuspto-grants-2006_11