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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 519621Generated: October 24, 2026

3-Ethoxy-2-methyl-3-oxopropane-1-diazonium → HCID 178438641, compound

https://huagongshe.com/en/reaction/519621

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Ethoxy-2-methyl-3-oxopropane-1-diazoniumHCID 86644035—
ReactantHCID 178438592HCID 178438592—
CatalystHCID 178476747HCID 178476747—
SolventTolueneHCID 1140—
ProductHCID 178438641HCID 17843864189%

Reaction Steps

To a mixture of 4′-{[4-(trans-4-hydroxycyclohexyl)-5-oxo-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl]methyl}biphenyl-2-carbonitrile (4 g), rhodium(I) acetate (0.028 g) and toluene (70 mL) was added dropwise a solution (10 mL) of 3-ethoxy-2-methyl-3-oxopropane-1-diazonium (5.5 mL) in toluene at 80° C., and the mixture was stirred at the same temperature for 1 hr. The reaction mixture was concentrated, and the obtained residue was purified by silica gel column chromatography. The obtained residue was dissolved in tetrahydrofuran (20 mL) and methanol (20 mL), and 1N aqueous sodium hydroxide solution (20 mL) was added. The reaction mixture was stirred for 1 hr, 1N aqueous hydrochloric acid solution was added, and the mixture was extracted with ethyl acetate. The obtained ethyl acetate layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to give the title compound as a colorless solid (4.1 g, 89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115136B2
Source datasetuspto-grants-2015_08
ORD IDord-1a9e26cb03544b168892c6f25fdac07f
Source noteuspto-grants-2015_08