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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1431420Generated: November 4, 2026

2,5-Dimorpholinobenzenamine → N-(2,5-di-4-morpholinylphenyl)-5,7-difluoro-3-methyl-2-(2-(methylsulfonyl)phenyl)-4-quinolinamine

https://huagongshe.com/reaction/1431420

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-DimorpholinobenzenamineHCID 28809815—
Reactant4-Chloro-5,7-difluoro-3-methyl-2-(2-(methylsulfonyl)phenyl)quinolineHCID 59631037—
SolventTolueneHCID 1140—
ProductN-(2,5-di-4-morpholinylphenyl)-5,7-difluoro-3-methyl-2-(2-(methylsulfonyl)phenyl)-4-quinolinamineHCID 67509138—

Reaction Steps

Prepared according to Procedure H using 4-chloro-5,7-difluoro-3-methyl-2-(2-(methylsulfonyl)phenyl)quinoline (39.0 mg, 0.110 mmol) and 2,5-dimorpholinoaniline in toluene to give N-(2,5-di-4-morpholinylphenyl)-5,7-difluoro-3-methyl-2-(2-(methylsulfonyl)phenyl)-4-quinolinamine. 1H NMR (CDCl3) δ ppm 8.21 (2H, d, J=7.6 Hz), 7.78 (1H, t, J=7.6 Hz), 7.69 (1H, t, J=7.2 Hz), 7.47 (1H, d, J=9.2 Hz), 7.40 (1H, d, J=7.4 Hz), 6.98-7.09 (2H, m), 6.40 (1H, br. s.), 6.24 (1H, br. s.), 3.90 (4H, m), 3.78 (4H, m), 2.74-3.33 (8H, m), 1.95 (3H, m). Mass Spectrum (ESI) m/e=595.3 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940724B2
Source datasetuspto-grants-2015_01
ORD IDord-407bf5244b9a4546a1730d4fa4afb909
Source noteuspto-grants-2015_01