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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1398172Generated: November 1, 2026

3-methoxy-4-(4-methyl-1H-imidazol-1-yl)benzohydrazide → ethyl 8-(3,4-difluorophenyl)-3-[3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl]-5,6,7,8-tetrahydro[1,2,4]triazolo[4,3-a]pyridine-8-carboxylate

https://huagongshe.com/reaction/1398172

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-methoxy-4-(4-methyl-1H-imidazol-1-yl)benzohydrazideHCID 66607850—
ReactantEthyl 3-(3,4-difluorophenyl)-2-(methylsulfanyl)-3,4,5,6-tetrahydropyridine-3-carboxylateHCID 66608443—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Productethyl 8-(3,4-difluorophenyl)-3-[3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl]-5,6,7,8-tetrahydro[1,2,4]triazolo[4,3-a]pyridine-8-carboxylateHCID 6660847945.9%

Reaction Conditions

Temperature90 °C

Reaction Steps

3-Methoxy-4-(4-methyl-1H-imidazol-1-yl)benzohydrazide (236 mg) was added to a mixture of ethyl 3-(3,4-difluorophenyl)-2-(methylsulfanyl)-3,4,5,6-tetrahydropyridine-3-carboxylate (300 mg) in ethanol (3 mL) at room temperature, and the mixture was stirred at 90° C. for 2 days. The reaction mixture was diluted with ethyl acetate, the mixture was washed with water and saturated brine and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (NH, ethyl acetate/hexane) to give the title compound (217 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901309B2
Source datasetuspto-grants-2014_12
ORD IDord-0835a7a82d6442fea10806d37bb56315
Source noteuspto-grants-2014_12