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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678117Generated: November 3, 2026

Piperazine → 1-Phenyl-2-piperazin-1-yl-1H-indole-3-carboxaldehyde

https://huagongshe.com/reaction/1678117

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant1,4-DioxaneHCID 31275—
Reactant2-chloro-1-phenyl-1H-indole-3-carbaldehydeHCID 314793—
SolventWaterHCID 962—
Product1-Phenyl-2-piperazin-1-yl-1H-indole-3-carboxaldehydeHCID 5399683136.4%

Reaction Steps

A mixture of 2-chloro-1-phenyl-1H-indole-3-carboxaldehyde (2.0 g, 7.83 mmol), piperazine (6.73 g, 78.3 mmol) and dioxane (25 mL) is heated at reflux overnight. After cooling to room temperature, water (100 mL) is added and after 1 hr the solids are collected by filtration, washed with water and purified by flash chromatography eluting with chloroform-5% methanol. Product containing fractions are combined and concentrated to afford 2-(piperazin-1-yl)-1-phenyl-1H-indol-3-carboxaldehyde (0.87 g, 36%) as a beige solid. A sample, mp 175° C., is purified by flash chromatography eluting with dichloromethane-5% methanol. NMR (CDCl3) 10.29 (1H, s), 8.27 (1H, d), 7.60 (2H, m), 7.51 (1H, t), 7.40 (2H, d), 7.23 (1H, m), 7.15 (1H, t), 6.98 (1H, d), 3.27 (4H, m), 2.78 (4H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008491B2
Source datasetuspto-grants-2011_08
ORD IDord-c6c7a7d2d2284d84928e129c421800e8
Source noteuspto-grants-2011_08