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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1717339Generated: October 26, 2026

Methyl acetoacetate → 1-{4-[(ethylamino)carbonyl]-2-hydroxyphenyl}-5-methyl-1H-1,2,3-triazole-4-carboxylic acid

https://huagongshe.com/reaction/1717339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl acetoacetateHCID 7757—
ReactantSodium HydroxideHCID 14798—
ReactantSodium ethoxideHCID 2723922—
Reactant4-azido-N-ethyl-3-hydroxybenzamideHCID 86629807—
SolventEthanolHCID 702—
Product1-{4-[(ethylamino)carbonyl]-2-hydroxyphenyl}-5-methyl-1H-1,2,3-triazole-4-carboxylic acidHCID 6851619655%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 4-azido-N-ethyl-3-hydroxybenzamide (0.41 g) obtained in Example 133b) and methyl 3-oxobutanoate (0.27 ml) in ethanol (10 ml) was added 28% sodium ethoxide in ethanol solution (1.0 ml) at room temperature, and the mixture was stirred overnight and at 60° C. for 9 hr. After allowing to cool to room temperature, 1N aqueous sodium hydroxide solution (4.0 ml) was added to the reaction mixture and the mixture was stirred at room temperature overnight. The solvent was evaporated under reduced pressure, and the obtained residue was diluted with water. The obtained aqueous solution was washed with ethyl acetate, acidified with 1N hydrochloric acid, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure to give a crude product of the title compound as a brown solid (0.32 g, 55%). The obtained crude product was used for the next reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803822B2
Source datasetuspto-grants-2010_09
ORD IDord-dc61466282f64fc4b88180528d4d791e
Source noteuspto-grants-2010_09