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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1923608Generated: October 29, 2026

Isopropylamine → 2-[(E)-2-(3-Butyl-5-methyl-isoxazol-4-yl)-vinyl]-4-methyl-thiazole-5-carboxylic acid isopropylamide

https://huagongshe.com/reaction/1923608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropylamineHCID 6363—
ReactantTrimethylaluminumHCID 16682925—
Reactant2-[(E)-2-(3-Butyl-5-methyl-isoxazol-4-yl)-vinyl]-4-methyl-thiazole-5-carboxylic acid methyl esterHCID 66643651—
SolventTolueneHCID 1140—
Solvent1,4-DioxaneHCID 31275—
Product2-[(E)-2-(3-Butyl-5-methyl-isoxazol-4-yl)-vinyl]-4-methyl-thiazole-5-carboxylic acid isopropylamideHCID 4978093068%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a stirred solution of isopropylamine (59 mg, 1.0 mmol) in dioxane (2 mL) under argon and at room temperature was added trimethylaluminium (0.50 mL of a 2M solution in toluene, 1.0 mmol). After 1 h, a solution of 2-[(E)-2-(3-butyl-5-methyl-isoxazol-4-yl)-vinyl]-4-methyl-thiazole-5-carboxylic acid methyl ester (80 mg, 0.25 mmol) in dioxane (2 mL) was added and the reaction mixture warmed to 90° C. After 48 h, the reaction mixture was cooled, quenched with Seignettes's salt solution (2 mL) and water (2 mL), then extracted with ethyl acetate. The combined organic extracts were dried, filtered and concentrated. Purification by chromatography (silica, 10 to 80% ethyl acetate in heptane) gave the title compound (59 mg, 68%) as pale yellow solid. MS: m/e=348.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178522B2
Source datasetuspto-grants-2012_05
ORD IDord-d65ea5a1853a4a9088bb0068f79130b6
Source noteuspto-grants-2012_05