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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720410Generated: October 24, 2026

Phenacyl bromide → 1-Benzoyl-3-cyano-4-methyl-pyrrolo[1,2-a]quinoline

https://huagongshe.com/en/reaction/720410

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacyl bromideHCID 6259—
Reactant3-MethylquinolineHCID 11926—
ReactantHCID 21892121HCID 21892121—
SolventAcetonitrileHCID 6342—
Product1-Benzoyl-3-cyano-4-methyl-pyrrolo[1,2-a]quinolineHCID 10425501—

Reaction Steps

3-Methyl-1-phenacyl-quinolinium bromide: The title compound was prepared from 2-bromo-1-phenyl-ethanone (481 mg, 2.405 mmol), 3-methyl-quinoline (296 mg, 2.08 mmol) and acetonitrile (5 mL), similar to Example 1a, and yielded 640 mg (89%) as an off white solid: 1H NMR (CDCl3) 0.38 (d, J=1.8 Hz, 1H), 8.74 (s, 1H), 8.31 (m, 1H), 8.28 (m, 1H), 8.17 (dd, J=1.5, 8.4 Hz, 1H), 8.01 (m, 1H), 7.94–7.87 (m, 2H), 7.71 (m, 1H), 7.57 (t, J=7.8 Hz, 2H), 7.49 (s, 2H), 2.81 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135480B2
Source datasetuspto-grants-2006_11
ORD IDord-75840e5472614453991df0df02d35f8d
Source noteuspto-grants-2006_11