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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2305424Generated: October 25, 2026

4-Amino-3,5-dichlorobenzotrifluoride → 4-[[4-[2,6-Dichloro-4-(trifluoromethyl)anilino]pyrimidin-2-yl]amino]benzonitrile

https://huagongshe.com/reaction/2305424

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-3,5-dichlorobenzotrifluorideHCID 141094—
Reactant2-[(4-Cyanophenyl)amino]4-pyrimidinyl trifluoromethanesulfonateHCID 22398451—
Solvent1,4-DioxaneHCID 31275—
Product4-[[4-[2,6-Dichloro-4-(trifluoromethyl)anilino]pyrimidin-2-yl]amino]benzonitrileHCID 4887749.2%

Reaction Conditions

Temperature170 °C

Reaction Steps

2-[(4-cyanophenyl)amino]-4-pyrimidinyl trifluoromethanesulfonate (0.0022 mol) and 2,6-dichloro-4-(trifluoromethyl)-benzenamine (0.0044 mol) were combined in 1,4-dioxane (2.5 ml) and heated in a sealed tube under Ar at 170° C. for 40 hours. The reaction mixture was allowed to cool to room temperature. Silica gel was added, and the solvent was evaporated. The residue was purified by flash column chromatography over silica gel (eluent gradient: CH2Cl2:CH3OH:NH4OH 100:0:0 to 97:2.7:0.3). The desired fractions were collected and the solvent was evaporated. The residue was recrystallized from CH3CN, filtered off and dried, yielding 0.086 g (9.2%) of 4-[[4-[[2,6-dichloro-4-(trifluoromethyl)-phenyl ]amino]-2-pyrimidinyl]amino]benzonitrile (compound 66).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06440986B2
Source datasetuspto-grants-2002_08
ORD IDord-c171c555fb514c63893acf4f02f7dbf5
Source noteuspto-grants-2002_08