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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807494Generated: October 30, 2026

Isopropylamine → 6-(3-Butyl-5-methyl-isoxazol-4-ylmethoxy)-N-isopropyl-nicotinamide

https://huagongshe.com/reaction/1807494

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropylamineHCID 6363—
ReactantTrimethylaluminumHCID 16682925—
Reactant6-(3-Butyl-5-methyl-isoxazol-4-ylmethoxy)-nicotinic acid methyl esterHCID 66599158—
SolventTolueneHCID 1140—
Solvent1,4-DioxaneHCID 31275—
ProductDiisopropyl EtherHCID 7914—
Product6-(3-Butyl-5-methyl-isoxazol-4-ylmethoxy)-N-isopropyl-nicotinamideHCID 4980475630.6%

Reaction Conditions

Temperature90 °C

Reaction Steps

Trimethylaluminium (3 mL of a 2 M solution in toluene, 6 mmol) was added dropwise to a stirred solution of isopropylamine (355 mg, 6.0 mmol) in dioxane (4 mL) at room temperature and under argon. After 1 h, a solution of 6-(3-butyl-5-methyl-isoxazol-4-ylmethoxy)-nicotinic acid methyl ester (537 mg, 1.5 mmol) in dioxane (4 mL) was added and the reaction mixture warmed to 90° C. After 2 h the reaction mixture was cooled and poured onto ice/water. The resultant mixture was extracted with ethyl acetate then the combined extracts were washed with Seignette salt solution. The organic phase was dried, filtered and evaporated then purified by chromatography (silica, 0 to 60% ethyl acetate in heptane) then trituration with diisopropyl ether to give the title compound (76 mg, 15%) as a white solid. MS: m/e=332.4 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357703B2
Source datasetuspto-grants-2013_01
ORD IDord-32b91403c47441a58bc7cde75647b43a
Source noteuspto-grants-2013_01