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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443228Generated: October 30, 2026

Phosgene → N-{1-(4 Cyanobenzyl)-1H-imidazol-5-yl-aminocarbonyl}-4-(2-methylbenzyl) isonipecotic acid methyl ester

https://huagongshe.com/reaction/443228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosgeneHCID 6371—
ReactantTriethylamineHCID 8471—
ReactantHCID 21193372HCID 21193372—
ReactantHCID 21193404HCID 21193404—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductN-{1-(4 Cyanobenzyl)-1H-imidazol-5-yl-aminocarbonyl}-4-(2-methylbenzyl) isonipecotic acid methyl esterHCID 54079200—

Reaction Steps

To a suspension of 4-(2-methylbenzyl)-isonipecotic acid methyl ester hydrochloride (50 mg, 0.176 mmol) in toluene (2 ml) was added phosgene (0.912 ml of a 1.93M solution in toluene, 1.76 mmol) and triethylamine (0.074 ml, 0.528 mmol) and the mixture stirred for 48 hrs at room temperature. The excess phosgene was removed by purging the solution with argon gas for 10 min. The suspension was added to 1-(4-cyanobenzyl)-5-amino-1H-imidazole hydrochloride (100 mg, 0.528 mmol) in CH2Cl2 (10 ml) and the mixture stirrred at 50° C. for 72 hrs. The solvent was evaporated in vacuo and the residue purified by preparative HPLC (C18, 95:5 to 5:95 water: acetonitrile containing 0.1% TFA). The residue after lyophilisation was partitioned between CH2Cl2 and saturated NaHCO3 solution. The organic extract was dried (MgSO4), and evaporated to dryness

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05891889
Source datasetuspto-grants-1999_04
ORD IDord-33bee21362fb44778c596e4253399cdd
Source noteuspto-grants-1999_04