Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250073Generated: October 26, 2026

5-Methoxyindoleacetic acid → 1-[(5-methoxy-1H-indol-3-yl)methylcarbonyl]-4-(4-nitrophenyl)-piperazine

https://huagongshe.com/reaction/1250073

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Methoxyindoleacetic acidHCID 18986—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant1-(4-Nitrophenyl)piperazineHCID 80447—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product1-[(5-methoxy-1H-indol-3-yl)methylcarbonyl]-4-(4-nitrophenyl)-piperazineHCID 2191870791%

Reaction Steps

In a 100 ml flask, 1.62 g (10 mmoles) of 1.1′-carbonyl-diimidazole is added to a solution of 2.05 g (10 mmoles) of 5-methoxyindole-3-acetic acid in 10 ml of THF. After one hour of agitation at ambient temperature, a solution of 1-(4-nitrophenyl)piperazine in 10 ml of DMF is added dropwise. Agitation is continued for 15 hours. The reaction medium is then concentrated under vacuum and the evaporation residue is precipitated from 50 ml of an ethyl acetate/water mixture (1/1). After filtration, the solid is rinsed successively with 50 ml of water, 50 ml of ethyl acetate and 50 ml of dichloromethane. After drying under vacuum, a yellow powder is obtained with a yield of 91%. Melting point: 239-240° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06335445B1
Source datasetuspto-grants-2002_01
ORD IDord-8a8dbd518b0a4e7eb84df2c6f0a12c0e
Source noteuspto-grants-2002_01