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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1477674Generated: November 2, 2026

Trifluoroacetic acid → HCID 136933045, compound

https://huagongshe.com/reaction/1477674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 117839254HCID 117839254—
ReactantHCID 117839615HCID 117839615—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 136933045HCID 13693304594%

Reaction Steps

To 1-(4-methoxybenzyl)-6-methyl-4-(methylthio)-1,3,5-triazin-2(1H)-one (1.39 g, 5.0 mmol) synthesized in Reference Synthesis Example 315, trifluoroacetic acid (10 mL) was added and the resultant mixture was stirred for 1 hour under reflux. After completion of the reaction, the reaction solution was concentrated under reduced pressure and 1,4-dioxane (10 mL), (R)-4-(4-fluorophenyl)-1,2,3,6-tetrahydropyridin-3-ol (966 mg, 5.00 mmol) synthesized in Reference Synthesis Example 133, and N,N-diisopropylethylamine (1.92 g, 10.0 mmol) were added to the concentrated solution, followed by refluxing the resultant mixture for 2 hours. After completion of the reaction, water was added to the reaction solution and extraction from the resultant mixture with ethyl acetate was performed. The organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (ethyl acetate/methanol=10/1) to obtain the title compound (1.41 g, yield 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403798B2
Source datasetuspto-grants-2016_08
ORD IDord-3e4bfc40dd2840d2a0f3dda37410cb75
Source noteuspto-grants-2016_08