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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1988331Generated: October 26, 2026

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

https://huagongshe.com/reaction/1988331

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant5-Methoxyindoleacetic acidHCID 18986—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant1-(4-Nitrophenyl)piperazineHCID 80447—
SolventDimethylformamideHCID 6228—
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 numberUS07553976B2
Source datasetuspto-grants-2009_06
ORD IDord-f38f3c5f00a54d0887a7b0fd00eeb38e
Source noteuspto-grants-2009_06