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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 83302Generated: October 29, 2026

Diisopropylethylamine → 6-{[3-(4-Fluoro-phenyl)-5-methyl-isoxazol-4-ylmethyl]-amino}-nicotinic acid methyl ester

https://huagongshe.com/reaction/83302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethyl 6-chloropyridine-3-carboxylateHCID 254249—
ReactantC-[3-(4-Fluoro-phenyl)-5-methyl-isoxazol-4-yl]-methylamineHCID 28750529—
SolventDimethyl SulfoxideHCID 679—
Product6-{[3-(4-Fluoro-phenyl)-5-methyl-isoxazol-4-ylmethyl]-amino}-nicotinic acid methyl esterHCID 6844339233%

Reaction Conditions

Temperature160 °C

Reaction Steps

A mixture of C-[3-(4-fluoro-phenyl)-5-methyl-isoxazol-4-yl]-methylamine (620 mg, 3.0 mmol), methyl 6-chloronicotinate (516 mg, 3.0 mmol), N,N-diisopropyl ethyl amine (1.0 mL, 6.0 mmol) and DMSO (6 mL) was heated in the microwave to 160° C. for 2 h. The mixture was then diluted with ice-water and extracted with ethyl acetate. The combined organic extracts were then washed with brine and dried over sodium sulfate. Concentration and purification by chromatography (SiO2, heptane:ethyl acetate=100:0 to 1:1 then dichloromethane:methanol 97:3) afforded the title compound (335 mg, 33%) as a white foam. MS: m/e=342.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846719B2
Source datasetuspto-grants-2014_09
ORD IDord-89a064fe3c6943a98a4a8c860306e259
Source noteuspto-grants-2014_09