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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1947342Generated: October 30, 2026

Potassium Iodide → methyl 8-(1-((3,5-difluorophenyl)(methyl)amino)ethyl)-2-morpholino-4-oxo-4H-chromene-6-carboxylate

https://huagongshe.com/reaction/1947342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant3,5-difluoro-N-methylanilineHCID 16720377—
Reactantmethyl 8-(1-bromoethyl)-2-morpholino-4-oxo-4H-chromene-6-carboxylateHCID 58234984—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
Productmethyl 8-(1-((3,5-difluorophenyl)(methyl)amino)ethyl)-2-morpholino-4-oxo-4H-chromene-6-carboxylateHCID 5823502281.2%

Reaction Steps

Potassium iodide (1.521 g, 9.16 mmol) was added to a suspension of methyl 8-(1-bromoethyl)-2-morpholino-4-oxo-4H-chromene-6-carboxylate (3.3 g, 8.33 mmol, as described in Example 2.00) and 3,5-difluoro-N-methylaniline (3.58 g, 24.99 mmol) in CHCl3 (16 mL) and MeOH (4 mL). The mixture was stirred at RT over the weekend. The reaction mixture was concentrated to dryness and the resulting dark oil was triturated with diethyl ether to give a solid which was collected by filtration. This solid was suspended in water and pH was adjusted to 6-7 with 2N NaOH. The crude product was filtered and washed with ether, dried and purified by flash chromatography on silica gel eluting with 0 to 10% MeOH in DCM. The solvent was evaporated to dryness to afford methyl 8-(1-((3,5-difluorophenyl)(methyl)amino)ethyl)-2-morpholino-4-oxo-4H-chromene-6-carboxylate (3.1 g, 81%) as a white solid. Mass Spectrum: M+H+ 459.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399460B2
Source datasetuspto-grants-2013_03
ORD IDord-4b227514d3e44046a92dab7753ddc65b
Source noteuspto-grants-2013_03