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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1923561Generated: November 1, 2026

4-Aminotetrahydropyran → 2-[(e)-2-(5-Methyl-3-phenyl-isoxazol-4-yl)-vinyl]-thiazole-5-carboxylic acid(tetra-hydro-pyran-4-yl)-amide

https://huagongshe.com/reaction/1923561

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminotetrahydropyranHCID 419223—
ReactantTrimethylaluminumHCID 16682925—
ReactantHCID 66643683HCID 66643683—
SolventTolueneHCID 1140—
Solvent1,4-DioxaneHCID 31275—
Product2-[(e)-2-(5-Methyl-3-phenyl-isoxazol-4-yl)-vinyl]-thiazole-5-carboxylic acid(tetra-hydro-pyran-4-yl)-amideHCID 4978180759%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a stirred solution of 4-aminotetrahydropyran (123 mg, 1.22 mmol) in dioxane (3 mL) under argon and at room temperature was added trimethylaluminium (0.6 mL of a 2M solution in toluene, 1.2 mmol). After 1 h, a solution of 2-[(E)-2-(5-methyl-3-phenyl-isoxazol-4-yl)-vinyl]-thiazole-5-carboxylic acid ethyl ester (50 mg, 0.15 mmol) in dioxane (3 mL) was added and the reaction mixture heated at 90° C. for 3 h. The reaction mixture was then cooled, quenched with ice water and extracted with dichloromethane. The combined extracts were washed with Seignette's salt solution then dried, filtered, and concentrated. Purification by chromatography (silica, 0 to 2.5% methanol in dichloromethane) gave the title compound (34 mg, 59%) as a white solid. MS: m/e=396.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178522B2
Source datasetuspto-grants-2012_05
ORD IDord-e81960e92c454ae1a7622ce43806fe75
Source noteuspto-grants-2012_05