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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20974Generated: October 26, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → tert-butyl 4-(1H-indol-5-ylcarbonyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/20974

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1H-Indole-5-Carboxylic AcidHCID 74280—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Producttert-butyl 4-(1H-indol-5-ylcarbonyl)piperazine-1-carboxylateHCID 42535715110.5%

Reaction Steps

Indole-5-carboxylic acid (1.00 g, 6.21 mmol) was dissolved in DMF (10 mL) and the solution was added with EDCI (2.38 g, 12.4 mmol), HOBT monohydrate (839 mg, 6.21 mmol) and 1-(tert-butoxycarbonyl)piperazine (1.73 g, 9.29 mmol), followed by stirring at room temperature for 3.5 hours. The reaction mixture was added with water and extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium hydrogencarbonate solution, 1 mol/L hydrochloric acid, and saturated brine, and was dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to obtain 5-[4-(tert-butoxycarbonyl)piperazin-1-ylcarbonyl]indole (2.26 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745641B2
Source datasetuspto-grants-2010_06
ORD IDord-0e0e4a05986a4ec39bc874b0966e8509
Source noteuspto-grants-2010_06