Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 245185Generated: October 30, 2026

N-bromobutanimide → Methyl 3-(bromomethyl)-7-[(1-methylethyl)oxy]-6-(methylsulfonyl)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate

https://huagongshe.com/reaction/245185

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl 3-methyl-7-[(1-methylethyl)oxy]-6-(methylsulfonyl)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylateHCID 67417507—
SolventCarbon TetrachlorideHCID 5943—
ProductMethyl 3-(bromomethyl)-7-[(1-methylethyl)oxy]-6-(methylsulfonyl)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylateHCID 67418621—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of methyl 3-methyl-7-[(1-methylethyl)oxy]-6-(methylsulfonyl)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate (2.97 g, 6.17 mmol), NBS (1.427 g, 8.02 mmol) and diphenylperoxyanhydride (0.149 g, 0.617 mmol) in carbon tetrachloride (30 mL) was heated to 100° C. and stirred overnight. The mixture was cooled to room temperature, and the solvent was removed under reduced pressure to give methyl 3-(bromomethyl)-7-[(1-methylethyl)oxy]-6-(methylsulfonyl)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate. This material was used without further purification. MS (m/z) 562.0 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658636B2
Source datasetuspto-grants-2014_02
ORD IDord-02446f0d54ea4876b1b7d102a14e1d65
Source noteuspto-grants-2014_02