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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725571Generated: October 31, 2026

Hydrochloric Acid → HCID 11245973, compound

https://huagongshe.com/reaction/1725571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-(3-Fluorophenyl)ethanamineHCID 533928—
ReactantHCID 58921890HCID 58921890—
ReactantHCID 178418255HCID 178418255—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 11245973HCID 1124597346%

Reaction Conditions

Temperature20 °C

Reaction Steps

Phenyl magnesium bromide (1M solution in THF, 0.0021 mol) was added to a solution of 3-fluoro-phenethyl amine (0.27 mL, 0.0021 mol) in anhydrous toluene (20 mL). After stirring the mixture at 20° C. for 10 min, 2-isopropyl-3-(2-methoxy-benzoylamino)-but-3-enoic acid methyl ester of step (b) above in this method (Method B of Example 13) (0.05 g, 0.0017 mol) was added. The mixture was refluxed for 10 hours, cooled and ethyl acetate (50 mL) was added followed by 1N HCl (50 mL). The organic layer was separated and the aqueous layer was extracted with EtOAc (3×50 mL). The combined organic extracts were washed with 1N HCl (3×100 mL), water (100 mL), and brine (100 mL). After drying over sodium sulfate and concentration on a rotatory evaporator, the product was purified by column chromatography over silica gel (200-400 mesh) eluting with 12% EtOAc/hexanes to give 3-[2-(3-fluoro-phenyl)-ethyl]-5-isopropyl-2-(2-methoxy-phenyl)-6-methyl-3H-pyrimidin-4-one (0.3 g, 46%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491728B2
Source datasetuspto-grants-2009_02
ORD IDord-982f8ae4993f41619c36dcc3beea3d16
Source noteuspto-grants-2009_02