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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 625220Generated: October 26, 2026

3-(Trifluoromethyl)benzylamine → 6-(2-nitro-5-(piperidin-1-yl)phenyl)-N-(3-(trifluoromethyl)benzyl)-pyrimidin-4-amine

https://huagongshe.com/reaction/625220

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)benzylamineHCID 75962—
Reactant4-Chloro-6-(2-nitro-5-(piperidin-1-yl)phenyl)pyrimidineHCID 86705928—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product6-(2-nitro-5-(piperidin-1-yl)phenyl)-N-(3-(trifluoromethyl)benzyl)-pyrimidin-4-amineHCID 6658682567.9%

Reaction Conditions

Temperature50 °C

Reaction Steps

Into a 50-mL round-bottom flask, was placed a solution of 4-chloro-6-(2-nitro-5-(piperidin-1-yl)phenyl)pyrimidine (191 mg) in N,N-dimethylformamide (10 mL), and 3-(trifluoromethyl)benzylamine (210 mg). The resulting solution was stirred overnight at 50° C. The resulting mixture was dissolved in 50 mL of ethyl acetate and washed with 2×50 mL of water. The mixture was dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was purified by silica gel chromatograpy to give 186 mg of product as yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09301951B2
Source datasetuspto-grants-2016_04
ORD IDord-9569472dcf744067ac12e260b3b8f2ea
Source noteuspto-grants-2016_04