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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655123Generated: October 26, 2026

2-Ethyl-4-(2-aminoethyl)-1-[2'-(1-trityl-1H-tetrazol-5-yl)biphenyl-4-yl]methylimidazole → ethyl 2-ethyl-3-[2'-(1-trityl-1H-tetrazol-5-yl)biphenyl-4-yl]methyl-4,5,6,7-tetrahydroimidazo[4,5-c]pyridine-4-carboxylate

https://huagongshe.com/reaction/1655123

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Ethyl-4-(2-aminoethyl)-1-[2'-(1-trityl-1H-tetrazol-5-yl)biphenyl-4-yl]methylimidazoleHCID 19932979—
ReactantEthyl glyoxylate hydrateHCID 22414697—
SolventTetrahydrofuranHCID 8028—
Productethyl 2-ethyl-3-[2'-(1-trityl-1H-tetrazol-5-yl)biphenyl-4-yl]methyl-4,5,6,7-tetrahydroimidazo[4,5-c]pyridine-4-carboxylateHCID 1993298665.2%

Reaction Steps

2-Ethyl-4-(2-aminoethyl)-1-[2'-(1-trityl-1H-tetrazol-5-yl)biphenyl-4-yl]methylimidazole (7.48 g) is dissolved in tetrahydrofuran (60 ml) to which is added ethyl glyoxylate hydrate (1.56 g). The reaction mixture is stirred overnight at room temperature and then refluxed for one hour. The solution is evaporated and the residue is purified by silica gel column chromatography (solvent; chloroform/methanol) to give ethyl 2-ethyl-3-[2'-(1 -trityl-1H-tetrazol-5-yl)biphenyl-4-yl]methyl-4,5,6,7-tetrahydroimidazo[4,5-c]pyridine-4-carboxylate (5.54 g) as a foam, characterized as its oxalate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05409936
Source datasetuspto-grants-1995_04
ORD IDord-1821f9831b2549538cf8eed73913c14e
Source noteuspto-grants-1995_04