Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2104511Generated: October 27, 2026

4-(Trifluoromethyl)benzenesulfonyl chloride → N-{3-[3-Benzoyl-8-(Trifluoromethyl)Quinolin-4-yl]Phenyl}-4-(Trifluoromethyl)Benzenesulfonamide

https://huagongshe.com/reaction/2104511

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)benzenesulfonyl chlorideHCID 2777399—
Reactant[4-(3-Aminophenyl)-8-(Trifluoromethyl)Quinolin-3-yl](Phenyl)MethanoneHCID 11326798—
ProductN-{3-[3-Benzoyl-8-(Trifluoromethyl)Quinolin-4-yl]Phenyl}-4-(Trifluoromethyl)BenzenesulfonamideHCID 11490334—

Reaction Steps

The title compound was prepared from [4-(3-aminophenyl)-8-(trifluoromethyl)quinolin-3-yl](phenyl)methanone and 4-(trifluoromethyl)benzenesulfonyl chloride following the procedure of Example 61 as an off-white solid: MS (EI) m/z 601.1 (M+H)+; 1H NMR (DMSO-d6): δ 7.00-7.10 (m, 3H), 7.24 (d, J=8.6 Hz, 1H), 7.33 (t, J=7.6 Hz, 2H), 7.50-7.60 (m, 3H), 7.70 (d, J=8.5 Hz, 1H), 7.75 (t, J=8.4 Hz, 1H), 7.87 (d, J=7.4 Hz, 2H), 7.96 (d, J=7.4 Hz, 2H), 8.34 (d, J=6.2 Hz, 1H), 9.11 (s, 1H), 10.65 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576215B2
Source datasetuspto-grants-2009_08
ORD IDord-c0eb74a8403f4086961e5d4b540555c1
Source noteuspto-grants-2009_08