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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070951Generated: 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/1070951

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 numberUS06903213B2
Source datasetuspto-grants-2005_06
ORD IDord-bd145d35e4714fe8bb3911bb5818d553
Source noteuspto-grants-2005_06