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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 83637Generated: October 30, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → ethyl 1-(1H-indole-2-carbonyl)piperidine-4-carboxylate

https://huagongshe.com/reaction/83637

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantEthyl 4-piperidinecarboxylateHCID 70770—
ReactantIndole-2-carboxylic acidHCID 72899—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Productethyl 1-(1H-indole-2-carbonyl)piperidine-4-carboxylateHCID 68380075—

Reaction Steps

1H-indole-2-carboxylic acid (2.49 g, 15.45 mmol), EDCI (4.44 g, 23.18 mmol), and HOBT (3.55 g, 23.18 mmol) were dissolved in THF (Volume: 30.0 ml). The reaction was allowed to stir for 15 minutes before DIEA (4.05 ml, 23.18 mmol) and ethyl piperidine-4-carboxylate (3.57 ml, 23.18 mmol) were added to the reaction. The reaction was diluted with water and ethyl acetate. The organic layer was washed with saturated sodium bicarbonate, 1H HCl, and saturated sodium chloride. The organic layer was then dried over magnesium sulfate, filtered and concentrated. the resulting solid is then triturated with ethyl acetate. (Yield: 3.27 g, white solid) 1H-NMR (400 MHz, DMSO-d6) 11.55, 7.60, 7.41, 7.18, 7.04, 6.77, 4.40-4.27, 4.09, 3.18, 2.76-2.63, 1.97-1.88, 1.65-1.51, 1.20

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846684B2
Source datasetuspto-grants-2014_09
ORD IDord-016e0bbf2c4d467488e5112edd4b84a3
Source noteuspto-grants-2014_09