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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1823938Generated: October 31, 2026

Citric Acid → HCID 178426694, compound

https://huagongshe.com/reaction/1823938

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant(4-Dimethylamino-butyl)-ethyl-carbodiimideHCID 21914090—
Reactant2-((Tert-butoxycarbonyl)amino)-3-(4-carbamoyl-2,6-dimethylphenyl)propanoic acidHCID 22147667—
ReactantHCID 178420113HCID 178420113—
SolventDimethylformamideHCID 6228—
ProductHCID 178426694HCID 178426694107.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-tert-Butoxycarbonylamino-3-(4-carbamoyl-2,6-dimethyl-phenyl)-propionic acid (0.42 g, 1.25 mmol) was dissolved in DMF (5 mL) followed by 1-hydroxybenzotriazole (0.34 g, 1.75 mmol), and the resulting solution was cooled to 0° C. To this reaction mixture was added 2-(4-phenyl-1H-imidazol-2-yl)-piperidine (0.31 g, 1.75 mmol) followed by (4-dimethylamino-butyl)-ethyl-carbodiimide (0.34 g, 1.75 mmol). The reaction was then warmed to room temperature and stirred for 16 hours. The reaction mixture was then combined with 2N citric acid and washed multiple times with ethyl acetate. The combined organics were washed with saturated aqueous NaHCO3, dried over Na2SO4, filtered, and concentrated under reduced pressure to yield 600 mg of desired product {1-(4-carbamoyl-2,6-dimethyl-benzyl)-2-oxo-2-[2-(4-phenyl-1H-imidazol-2-yl)-piperidin-1-yl]-ethyl}-carbamic acid tert-butyl ester as a glass which was used as is without further purification. (TLC: 5:1 CHCl3:MeOH Rf=0.6)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07041681B2
Source datasetuspto-grants-2006_05
ORD IDord-31901ece090a432f8d3c3420ae3a5c0b
Source noteuspto-grants-2006_05