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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 332388Generated: October 25, 2026

Dimethyl Sulfoxide → Methyl 6-(((5-methyl-3-phenylisoxazol-4-yl)methyl)amino)nicotinate

https://huagongshe.com/reaction/332388

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethyl 6-chloropyridine-3-carboxylateHCID 254249—
Reactant(5-Methyl-3-phenyl-4-isoxazolyl)-methylamineHCID 59594513—
SolventEthyl AcetateHCID 8857—
ProductMethyl 6-(((5-methyl-3-phenylisoxazol-4-yl)methyl)amino)nicotinateHCID 6844353946.1%

Reaction Conditions

Temperature160 °C

Reaction Steps

A mixture of (5-methyl-3-phenyl-4-isoxazolyl)-methylamine (200 mg, 1.06 mmol), methyl 6-chloronicotinate (182 mg, 1.06 mmol), N,N-diisopropyl ethyl amine (364 μL, 2.13 mmol) and DMSO (2 mL) was heated in the microwave to 160° C. for 0.5 h. It was diluted with ethyl acetate (8 mL) and washed with aqueous sodium carbonate (saturated, 8 mL), water (8 mL) and brine (8 mL). The combined aqueous layers were extracted with ethyl acetate (10 mL) and the combined organic layers were dried over sodium sulfate. Concentration and purification by chromatography (SiO2, heptane:ethyl acetate=100:0 to 50:50) afforded the title compound (158 mg, 46%) as a light yellow oil. MS: m/e=324.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877783B2
Source datasetuspto-grants-2014_11
ORD IDord-be8c7e9f13cb431397d981106424b8aa
Source noteuspto-grants-2014_11