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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 83288Generated: October 25, 2026

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

https://huagongshe.com/reaction/83288

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 numberUS08846719B2
Source datasetuspto-grants-2014_09
ORD IDord-d6f0e4ff98fb4548b255d2fe6f0dd391
Source noteuspto-grants-2014_09