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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678080Generated: October 30, 2026

Phenol → HCID 10053125, compound

https://huagongshe.com/reaction/1678080

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 86608508HCID 86608508—
SolventAcetonitrileHCID 6342—
ProductHCID 10053125HCID 1005312528.2%

Reaction Steps

81.3 mg (0.9 mmol) of phenol and 325.5 mg (2.4 mmol) of K2CO3 were added to 400.0 mg (0.78 mmol) of 1-(4-{4-[2-tert-butyl-6-(trifluoromethyl)pyrimidin-4-yl]piperazin-1-yl}butyl)-5-methyl-2-oxo-1,2-dihydropyrimidin-4-yl thiocyanate from Example 7.1 in 40 ml of acetonitrile and 500.0 mg of molecular sieves (3 Å). The reaction mixture was then stirred at room temperature for 12 hours. Insolubles were filtered off, methylene chloride was added to the filtrate, followed by extraction with aqueous brine. The residue after drying of the organic phase, removal of the desiccant by filtration and evaporation of the solvent in vacuo was taken up in 100 ml of diisopropyl ether and heated. The precipitate was filtered off with suction and the mother liquor was concentrated somewhat. The mother liquor was then mixed with pentane and cooled in an ice bath. The precipitated solid was filtered off with suction, washed and dried in vacuo at 40° C., resulting in 120 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008488B2
Source datasetuspto-grants-2011_08
ORD IDord-5957e51c99204e568774c3db9daeff0d
Source noteuspto-grants-2011_08