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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227006Generated: October 26, 2026

2-(Bromomethyl)-6-(trifluoromethyl)pyridine → 3-(4-Methoxy-3-methyl-benzoyl)-1-(6-trifluoromethyl-pyridin-2-ylmethyl)-1H-quinolin-4-one

https://huagongshe.com/reaction/227006

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Bromomethyl)-6-(trifluoromethyl)pyridineHCID 46941463—
Reactant3-(4-Methoxy-3-methyl-benzoyl)-1H-quinolin-4-oneHCID 57754758—
SolventDimethylformamideHCID 6228—
Product3-(4-Methoxy-3-methyl-benzoyl)-1-(6-trifluoromethyl-pyridin-2-ylmethyl)-1H-quinolin-4-oneHCID 5775455125.3%

Reaction Steps

Experimental conditions analogous to those described for Step 3 of Example 1 were used with 100 mg (0.341 mmol) of 3-(4-Methoxy-3-methyl-benzoyl)-1H-quinolin-4-one, 98.2 mg (0.409 mmol) of 2-bromomethyl-6-trifluoromethyl-pyridine, 16.4 mg (0.409 mmol, 60% dispersion in oil), and 3.5 mL of N,N-dimethylformamide. The crude product was purified by flash column chromatography using a gradient of 20-100% ethyl acetate in hexane to yield 39 mg of 3-(4-Methoxy-3-methyl-benzoyl)-1-(6-trifluoromethyl-pyridin-2-ylmethyl)-1H-quinolin-4-one. LC-MSD, m/z for C25H19F3N2O3 [M+H]: 453.13 LC retention time on HPLC, C18 column gradient 20-95% acetonitrile with 0.1% TFA in 4 minutes: 2.5 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557213B2
Source datasetuspto-grants-2009_07
ORD IDord-32ac805cfcff4326a42b618eebf8b70b
Source noteuspto-grants-2009_07