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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12427Generated: October 26, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → N-[3-Amino-2-hydroxy-3-oxo-1-(phenylmethyl)propyl]-2-(4-phenyl-1H-imidazol-1-yl)pyridine-3-carboxamide

https://huagongshe.com/reaction/12427

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Amino-2-hydroxy-4-phenylbutanamide hydrochlorideHCID 22593883—
Reactant2-(4-phenyl-1H-imidazol-1-yl)pyridine-3-carboxylic acidHCID 66720089—
ReactantHCID 178418300HCID 178418300—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductN-[3-Amino-2-hydroxy-3-oxo-1-(phenylmethyl)propyl]-2-(4-phenyl-1H-imidazol-1-yl)pyridine-3-carboxamideHCID 6672008237.3%

Reaction Conditions

Temperature2 °C

Reaction Steps

0.75 g of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC), 0.51 g of hydroxylbenzotriazole (HOBt) and 0.55 ml of triethylamine (Et3N) were successively added to a solution of 1.0 g of 2-(4-phenyl-1H-imidazol-1-yl)pyridine-3-carboxylic acid (3.77 mmol) in 50 ml of dichloromethane at 0-4° C., and the mixture was stirred at 0-4° C. for 1 hour. 0.9 g of 3-amino-2-hydroxy-4-phenylbutanamide hydrochloride (3.9 mmol) and 0.55 ml of Et3N were then added and, after about 5 minutes, a pH of 8-9 was adjusted by adding 0.5 ml of Et3N. The mixture was stirred at 0-4° C. for 1 hour and then at room temperature overnight. 50 ml of saturated NaHCO3 solution were then added to the mixture, and the organic phase was separated off. Drying and evaporating the solvent resulted in 620 mg of a reddish oil, which was reacted further immediately without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728012B2
Source datasetuspto-grants-2010_06
ORD IDord-6b46d268ecdb4ada8a7b6d15fb708a7b
Source noteuspto-grants-2010_06