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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1717277Generated: October 26, 2026

Hydrochloric Acid → 1-[4-({[2-(4-methylpiperazin-1-yl)ethyl]amino}carbonyl)phenyl]-5-propyl-1H-1,2,3-triazole-4-carboxylic acid

https://huagongshe.com/reaction/1717277

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl 3-oxohexanoateHCID 238498—
ReactantSodium ethoxideHCID 2723922—
Reactant4-azido-N-[2-(4-methylpiperazin-1-yl)ethyl]benzamideHCID 86629801—
SolventEthanolHCID 702—
Product1-[4-({[2-(4-methylpiperazin-1-yl)ethyl]amino}carbonyl)phenyl]-5-propyl-1H-1,2,3-triazole-4-carboxylic acidHCID 6851519698.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

4-Azido-N-[2-(4-methylpiperazin-1-yl)ethyl]benzamide obtained in Example 63b) and ethyl 3-oxohexanoate (0.503 ml, 2.99 mmol, 1.25 eq.) were dissolved in ethanol (15 ml), sodium ethoxide (226 mg, 2.99 mmol, 1.25 eq.) was added, and the mixture was stirred at room temperature for 30 min and at 60° C. for 10.5 hr. 1N hydrochloric acid (3.0 ml) was added to the reaction mixture, and the mixture was concentrated. The residue was diluted with acetonitrile (20 ml) and ethanol (40 ml), and the mixture was concentrated. Ethanol (15 ml), THF (20 ml) and ethyl acetate (20 ml) were added to the residue. The precipitate was collected by filtration, washed with ethyl acetate and dried to give the title compound as a pale-brown powder (purity 90%, containing sodium chloride, 1.04 g, 2.33 mmol, 98.2%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803822B2
Source datasetuspto-grants-2010_09
ORD IDord-dcdae3f03521438f92f668f382bb473a
Source noteuspto-grants-2010_09