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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326452Generated: October 30, 2026

Cyanoacetic acid → HCID 19736553, compound

https://huagongshe.com/reaction/326452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanoacetic acidHCID 9740—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 19736554HCID 19736554—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 19736553HCID 1973655393.7%

Reaction Steps

A mixture of methyl 2-n-butyl-1-{2'-(1-trityl-1H-tetrazol-5-yl)biphenyl-4-yl}methyl-4,5,6,7-tetrahydroimidazo[4,5-c]pyridine-6-carboxylate (0.81 g), dicyclohexyl-carbodiimide (0.26 g), 1-hydroxybenzotriazole (0.17 g), cyanoacetic acid (0.11 g) and acetonitrile (10 ml) is stirred at room temperature overnight. After the reaction is completed, ethyl acetate is added to the reaction mixture, and the mixture is waehed with aqueous sodium hydrogen carbonate solution, dried, and the solvent is distilled off under reduced pressure. The resulting residue is purified by silica gel column chromatography (solvent; ethyl acetate) to give methyl 2-n-butyl-5-cyanoacetyl-1-{2'-(1-trityl-1H-tetrazol-5-yl)biphenyl-4-yl}methyl-4,5,6,7-tetrahydroimidazo[4,5-c]pyridine-6-carboxylate (0.83 g) as foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05268377
Source datasetuspto-grants-1993_12
ORD IDord-adaf8ab1e0124c6b8eb08776ed52924e
Source noteuspto-grants-1993_12