Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929810Generated: November 2, 2026

Potassium Carbonate → 3-[4-(5-Fluoro-2-methyl-phenoxymethyl)-phenyl]-isoxazole-5-carboxylic acid amide

https://huagongshe.com/reaction/929810

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant5-Fluoro-2-methylphenolHCID 2774616—
Reactant1613166-38-3HCID 90202460—
SolventAcetonitrileHCID 6342—
Product3-[4-(5-Fluoro-2-methyl-phenoxymethyl)-phenyl]-isoxazole-5-carboxylic acid amideHCID 7628159669%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a mixture of 3-(4-bromomethyl-phenyl)-isoxazole-5-carboxylic acid amide (which may be prepared as described in Preparation of Intermediate 14; 30 mg, 0.107 mmol) in CH3CN (2 mL) were added 5-fluoro-2-methylphenol (20 μL. 0.18 mmoL) and K2CO3 (30 mg, 0.22 mmol). The mixture was heated at 90° C. for 16 h and then evaporated to dryness. The residue was purified by chromatography (66-75% EtOAc/hexanes) to give 3-[4-(5-fluoro-2-methyl-phenoxymethyl)-phenyl]-isoxazole-5-carboxylic acid amide (24 mg, 69%) as a white powder. 1H NMR (300 MHz, DMSO-d6) δ ppm 8.38 (br. s., 1H), 8.01 (br. s., 1H), 7.93 (d, J=8.2 Hz, 2H), 7.52-7.65 (m, 3H), 7.16 (t, J=7.5 Hz, 1H), 6.92 (dd, J=11.3, 2.6 Hz, 1H), 6.67 (td, J=8.5, 2.7 Hz, 1H), 5.20 (s, 2H), 2.16 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296711B2
Source datasetuspto-grants-2016_03
ORD IDord-b8a8616fe10e436ba5d485470555f013
Source noteuspto-grants-2016_03