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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1717272Generated: October 26, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 4-azido-N-(2-piperidin-1-ylethyl)benzamide

https://huagongshe.com/reaction/1717272

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantN-(2-Aminoethyl)piperidineHCID 33944—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant4-Azidobenzoic acidHCID 3034184—
SolventDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
Product4-azido-N-(2-piperidin-1-ylethyl)benzamideHCID 86629800—

Reaction Steps

4-Azidobenzoic acid (858 mg, 5.15 mmol), HOBt (704 mg, 5.15 mmol, 1.0 eq.) and N-(2-aminoethyl)piperidine (0.788 ml, 5.41 mmol, 1.05 eq.) were dissolved in acetonitrile (6 ml) and DMF (6 ml), WSC (1.21 g, 6.19 mmol, 1.2 eq.) was added, and the mixture was stirred at room temperature for 3 hr. The reaction mixture was concentrated, dissolved in ethyl acetate (50 ml) and washed with 5% aqueous sodium carbonate solution and saturated brine. The aqueous layers were each extracted with ethyl acetate (30 ml). The organic layers were combined, dried over anhydrous sodium sulfate and concentrated at 30° C. or below to give the title compound as a pale-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803822B2
Source datasetuspto-grants-2010_09
ORD IDord-07faf4668e75412ea650ba4abf495214
Source noteuspto-grants-2010_09