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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485120Generated: November 3, 2026

Potassium Carbonate → Ethyl 3-({[3-(4-chlorophenyl)-isoxazol-5-yl]methyl}amino)-3-methylbutanoate

https://huagongshe.com/reaction/1485120

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantIsoxazole, 5-bromomethyl-3-(p-chlorophenyl)-HCID 21369—
ReactantEthyl 3-amino-3-methylbutanoate hydrochlorideHCID 15578558—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-({[3-(4-chlorophenyl)-isoxazol-5-yl]methyl}amino)-3-methylbutanoateHCID 118113168—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of ethyl 3-amino-3-methylbutyrate hydrochloride (333 mg) in tetrahydrofuran (4.00 mL), a solution in tetrahydrofuran (2.00 mL) of the compound (100 mg) obtained in step (2) above and potassium carbonate (406 mg) were added and the mixture was stirred at 60° C. for three days. After passing the reaction mixture through Celite (registered trademark), the filtrate was concentrated under reduced pressure and the resulting residue was roughly purified by preparative HPLC. To the resulting roughly purified product, a saturated aqueous solution of sodium hydrogencarbonate was added and extraction was conducted with chloroform. The combined organic layers were dried over anhydrous magnesium sulfate and after removing the desiccant by filtration, the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=98:2-50:50) to give the titled compound as a colorless amorphous mass.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422240B2
Source datasetuspto-grants-2016_08
ORD IDord-bc78b860e859498dabe736749cb07bff
Source noteuspto-grants-2016_08