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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929789Generated: November 2, 2026

Potassium Carbonate → 3-[4-(2-Methanesulfonyl-benzyloxy)-phenyl]-isoxazole-5-carboxylic acid amide

https://huagongshe.com/reaction/929789

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-(Bromomethyl)-2-methanesulfonylbenzeneHCID 18922474—
Reactant3-(4-Hydroxy-phenyl)-isoxazole-5-carboxylic acid amideHCID 136491250—
CatalystTetrabutylammonium IodideHCID 67553—
SolventDimethylformamideHCID 6228—
Product3-[4-(2-Methanesulfonyl-benzyloxy)-phenyl]-isoxazole-5-carboxylic acid amideHCID 762807983.3%

Reaction Conditions

Temperature40 °C

Reaction Steps

3-(4-Hydroxy-phenyl)-isoxazole-5-carboxylic acid amide (which may be prepared as described in Preparation of Intermediate 2; 50 mg, 0.245 mmol) was dissolved in DMF (1.5 mL). K2CO3 (42 mg, 0.30 mmol), tetrabutylammonium iodide (14 mg, 0.038 mmol), and 1-bromomethyl-2-methylsulfonyl-benzene (which is available from Combi-Blocks; 62 mg, 0.25 mmol) were added. The reaction mixture was heated at 40° C. for 13 h. The reaction mixture was cooled to room temperature and partitioned between H2O (5 mL) and EtOAc (5 mL). The organic layer was dried (Na2SO4), filtered, evaporated, and purified twice by chromatography (40-60% EtOAc/hexanes) to give 3-[4-(2-methanesulfonyl-benzyloxy)-phenyl]-isoxazole-5-carboxylic acid amide (3 mg, 3%) as a white powder. HRMS Calcd. for C18H17N2O5S (M+H)+, 373.0853. Found: 373.0854.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296711B2
Source datasetuspto-grants-2016_03
ORD IDord-e3fc7104554e46f89e32614ad9c30756
Source noteuspto-grants-2016_03