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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 744724Generated: October 30, 2026

Ammonium formate → 4-[4-(4-fluorophenyl)-1-hydroxy-1-(4-tert-butylaminocarbonylphenyl)butyl]-1H-imidazole

https://huagongshe.com/reaction/744724

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant1-benzyl-5-[4-(4-fluorophenyl)-1-hydroxy-1-(4-tert-butylaminocarbonylphenyl)butyl]-1H-imidazole hydrochlorideHCID 19422014—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product4-[4-(4-fluorophenyl)-1-hydroxy-1-(4-tert-butylaminocarbonylphenyl)butyl]-1H-imidazoleHCID 17844931079%

Reaction Steps

1-benzyl-5-[4-(4-fluorophenyl)-1-hydroxy-1-(4-tert-butylaminocarbonylphenyl)butyl]-1H-imidazole hydrochloride (12,95 g) is dissolved into aqueous ethanol (400 ml) and 1,3 g of 10% Pd/C is added. Ammonium formate (8,17 g) is added to the boiling solution in small portions. The mixture is refluxed for three hours. Then the reaction mixture is filtered through siliceous earth and the filtrate is evaporated to dryness. The residue is dissolved to methylene chloride, washed with 2M sodiumhydroxide and water, dried and evaporated to dryness. Yield 79%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05559141
Source datasetuspto-grants-1996_09
ORD IDord-c16b678e3e844f2f9de1b75692c34f48
Source noteuspto-grants-1996_09