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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 83612Generated: October 26, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 66571156, compound

https://huagongshe.com/reaction/83612

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant3-MethylbenzylamineHCID 66015—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-(1-(4-chlorobenzyl)-1H-indole-2-carbonyl)piperidine-4-carboxylic acidHCID 57385796—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 66571156HCID 66571156—

Reaction Steps

1-(1-(4-chlorobenzyl)-1H-indole-2-carbonyl)piperidine-4-carboxylic acid (393 mg, 0.990 mmol), 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (237 mg, 1.23 mmol), and 1-Hydroxybenzotriazole (167 mg, 1.23 mmol) were dissolved in 2.0 mL of DCM. The reaction was allowed to stir for 10 minutes before N,N-Diisopropylethylamine (216 μL, 1.059 mmol) and m-tolylmethanamine (100 mg, 0.83 mmol) were added as a 1.0 mL DCM solution. The reaction was allowed to stir overnight. The reaction was diluted with water and ethyl acetate. The layers were separated and the organic layer was washed with another aliquot of water. The ethyl acetate layer was washed with 1N HCl followed by saturated sodium bicarbonate then saturated sodium chloride. The organic layer was dried over magnesium sulfate, filtered and concentrated. The crude material was triturated with methanol and filtered under vacuum to obtain pure product as a white solid. Yield: 190 mg (White solid)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846684B2
Source datasetuspto-grants-2014_09
ORD IDord-b96131a290f64217999e9a99eedd08a9
Source noteuspto-grants-2014_09