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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 265048Generated: November 1, 2026

5-(4'-(Bromomethyl)(1,1'-biphenyl)-2-yl)-1-trityl-1H-tetraazole → Diethyl 2-propyl-1-((2'-(1-trityl-1H-tetrazol-5-yl)-[1,1'-biphenyl]-4-yl)methyl)-1H-imidazole-4,5-dicarboxylate

https://huagongshe.com/reaction/265048

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(4'-(Bromomethyl)(1,1'-biphenyl)-2-yl)-1-trityl-1H-tetraazoleHCID 10053461—
Reactant1H-Imidazole-4,5-dicarboxylic acid, 2-propyl-, 4,5-diethyl esterHCID 10286015—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
SolventDimethylacetamideHCID 31374—
ProductDiethyl 2-propyl-1-((2'-(1-trityl-1H-tetrazol-5-yl)-[1,1'-biphenyl]-4-yl)methyl)-1H-imidazole-4,5-dicarboxylateHCID 1903608978%

Reaction Steps

0.441 g of potassium t-butoxide was added to a solution of 1.00 g of diethyl 2-propylimidazole-4,5-dicarboxylate (prepared as described in Preparation 12) in 15 ml of N,N-dimethylacetamide, and the resulting mixture was stirred at room temperature for 30 minutes. A solution of 2.19 g of 4-[2-(trityltetrazol-5-yl)phenyl]benzyl bromide in 15 ml of N,N-dimethylacetamide was then added dropwise to the reaction mixture at room temperature, and the reaction mixture was stirred at room temperature for 3 hours. At the end of this time, it was diluted with water and then extracting with ethyl acetate. The extract was dried over anhydrous magnesium sulfate and then freed from the solvent by distillation. The residue was purified by column chromatography through silica gel, using a 1:1 by volume mixture of hexane and ethyl acetate as the eluent,to give 2.24 g of the title compound as an amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05646171
Source datasetuspto-grants-1997_07
ORD IDord-a8235e7e2df64f21af021e61e719d521
Source noteuspto-grants-1997_07