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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 56289Generated: October 27, 2026

Toluene → 4-(2-fluoro-4-(2-((3-fluorophenoxy)methyl)-4-methyl-6-oxopyrimidin-1(6H)-yl)phenyl)morpholin-3-one

https://huagongshe.com/reaction/56289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-(3-Fluorophenoxy)acetamideHCID 18938105—
ReactantN-(3-fluoro-4-(3-oxomorpholino)phenyl)-3-oxobutanamideHCID 90023448—
CatalystTitanium isopropoxideHCID 11026—
SolventO-XyleneHCID 7237—
Product4-(2-fluoro-4-(2-((3-fluorophenoxy)methyl)-4-methyl-6-oxopyrimidin-1(6H)-yl)phenyl)morpholin-3-oneHCID 900232777%

Reaction Conditions

Temperature165 °C

Reaction Steps

A mixture of N-(3-fluoro-4-(3-oxomorpholino)phenyl)-3-oxobutanamide (0.59 g, 2.00 mmol), 2-(3-fluorophenoxy)acetamide (0.94 g, 5.56 mmol) and titanium tetraisopropanolate (4.8 mL) in xylene (10 mL) was stirred at 165° C. for 24 h. The mixture was cooled to rt and 60 mL of toluene and 60 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 (20 mL×4). The combined organic layers were washed with brine (30 mL×2), dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by a silica gel column chromatography (PE/EtOAc (V/V)=1:2) to give the title compound as a yellow solid (0.06 g, 7%). 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-2c19aa9b302d4a9eba58dcd2141ac008
Source noteuspto-grants-2016_09