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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 967775Generated: October 23, 2026

4-(Methylamino)benzoic acid → UP9V9DB2RD

https://huagongshe.com/en/reaction/967775

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Methylamino)benzoic acidHCID 66345—
ReactantSodium BicarbonateHCID 516892—
Reactant1-[2-(4-Cyanophenyl)ethyl]piperidin-4-spiro-2'-oxiraneHCID 85819721—
CatalystScandium(III) triflateHCID 2734571—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductUP9V9DB2RDHCID 1298648164.5%

Reaction Steps

Scandium trifluoromethanesulfonate (609 mg) was added to a mixture of the compound (500 mg) obtained in Step 3 of Example 1, 4-methylaminobenzoic acid (343 mg) and anhydrous acetonitrile (10 mL) under cooling with ice-water, and the mixture was stirred at room temperature for sixty eight hours under nitrogen atmosphere. Water (50 mL) and acetonitrile (10 mL) were added to the resulting mixture and the pH of the mixture was adjusted to above 9 with sodium hydrogen carbonate, insoluble matter was removed by filtration and the filtrate was concentrated under reduced pressure. Water in the residue was removed by azeotrope with ethanol, soluble components in the residue were dissolved in ethanol and the insoluble matter was removed by filtration. The filtrate was concentrated under reduced pressure and then, the residue was dissolved in water (50 mL) and the pH of the solution was adjusted to 7 by diluted hydrochloric acid. Precipitate was collected by filtration and washed with water and ethyl acetate successively under stirring. The precipitate was collected by filtration and dried to obtain the titled compound (524 mg) as powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06956046B2
Source datasetuspto-grants-2005_10
ORD IDord-4299d678945a4105be6f8c2c05d2b8d2
Source noteuspto-grants-2005_10