HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1407962Generated: October 30, 2026
3-(Trifluoromethyl)benzylamine → 6-(2-nitro-5-(piperidin-1-yl)phenyl)-N-(3-(trifluoromethyl)benzyl)-pyrimidin-4-amine
https://huagongshe.com/reaction/1407962
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-(Trifluoromethyl)benzylamine | HCID 75962 | — |
| Reactant | 4-Chloro-6-(2-nitro-5-(piperidin-1-yl)phenyl)pyrimidine | HCID 86705928 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 6-(2-nitro-5-(piperidin-1-yl)phenyl)-N-(3-(trifluoromethyl)benzyl)-pyrimidin-4-amine | HCID 66586825 | 67.9% |
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 chromatography to give 186 mg of product as yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08916569B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-71c88a9fa09b43c6802845e80222e82f |
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| Source note | uspto-grants-2014_12 |
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