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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 56296Generated: October 28, 2026

Toluene → 2-(difluoro(3-fluorophenoxy)methyl)-3-(3-fluoro-4-morpholinophenyl)-6-methyl-pyrimidin-4(3H)-one

https://huagongshe.com/reaction/56296

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantAmmonium ChlorideHCID 25517—
Reactant2,2-Difluoro-2-(3-fluorophenoxy)acetamideHCID 90022910—
ReactantN-(3-fluoro-4-morpholinophenyl)-3-oxobutanamideHCID 90023295—
CatalystTitanium isopropoxideHCID 11026—
SolventO-XyleneHCID 7237—
Product2-(difluoro(3-fluorophenoxy)methyl)-3-(3-fluoro-4-morpholinophenyl)-6-methyl-pyrimidin-4(3H)-oneHCID 9002306140%

Reaction Conditions

Temperature165 °C

Reaction Steps

A mixture of N-(3-fluoro-4-morpholinophenyl)-3-oxobutanamide (0.60 g, 2.14 mmol), 2,2-difluoro-2-(3-fluorophenoxy)acetamide (0.88 g, 4.29 mmol) and titanium tetraisopropanolate (4.87 g, 17.1 mmol) in xylene (20 mL) was stirred at 165° C. for 24 h. The mixture was cooled to rt and 60 mL of toluene and 80 mL of saturated NH4Cl aqueous solution were added. The resulting mixture was stirred at rt overnight and filtered and the filtrate was extracted with DCM (150 mL×3). The combined organic layers were dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by a silica gel column chromatography (PE/EtOAc (V/V)=1:1) to give the title compound as a yellow solid (0.38 g, 40%). The compound was characterized by the following spectroscopic data:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434695B2
Source datasetuspto-grants-2016_09
ORD IDord-15ae61c5b24a4e61bf8b2381320619c2
Source noteuspto-grants-2016_09