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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783516Generated: October 30, 2026

Trifluoroacetic acid → HCID 54320219, compound

https://huagongshe.com/reaction/1783516

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant4-(4-Methylpiperazin-1-yl)anilineHCID 737253—
ReactantHCID 68860079HCID 68860079—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 54320219HCID 5432021963%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a suspension of 300 mg (0.98 mmol) of 1-bicyclo[2.2.1]hept-2-yl-7-methanesulfinyl-3,4-dihydro-pyrimido[4,5-d]pyrimidin-2(1H)-one and 374 mg (1.96 mmol) of 1-(4-aminophenyl)-4-methylpiperazine in 4.0 mL of acetonitrile is added 377 μL (4.90 mmol) of trifluoroacetic acid. The mixture is heated at 85° C. overnight. The cooled reaction mixture is diluted with ethyl acetate and washed two times with saturated aqueous sodium bicarbonate solution and once with brine. The organic phase is dried over magnesium sulfate and concentrated. The dark solid residue is triturated in 4 mL of 1:1 dichloromethane/ethyl acetate, filtered, washed with ethyl acetate, and dried to give 266 mg (63%) of the title compound: mp 251-254° C. (dec).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501425B1
Source datasetuspto-grants-2009_03
ORD IDord-b934ffe6a7bf40dfa66cbe5b680555f5
Source noteuspto-grants-2009_03