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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238385Generated: October 29, 2026

1-Phenylpiperazine → HCID 86684883, compound

https://huagongshe.com/reaction/238385

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PhenylpiperazineHCID 7096—
ReactantTriethylamineHCID 8471—
ReactantHCID 86684882HCID 86684882—
SolventDimethylformamideHCID 6228—
ProductHCID 86684883HCID 86684883103.4%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 1-phenylpiperazine (3.40 g), 5-[(4-chlorobenzyl)oxy]-1-methyl-1H-pyrazol-4-carbaldehyde (600 mg), triethylamine (1.20 mL) and dimethylformamide (7.0 mL) was stirred at 120° C. for 8 hours, and then at a room temperature for 17 hours. Thereafter, the reaction solution was concentrated under a reduced pressure, and water was then added thereto. The obtained mixture was extracted with ethyl acetate. The organic layer was washed with water and a saturated saline, and was then dried over anhydrous sodium sulfate, followed by vacuum concentration. The residue was purified by column chromatography (silica gel cartridge, hexane:ethyl acetate=80:20 to 10:90), so as to obtain the title compound (669 mg) in the form of a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642626B2
Source datasetuspto-grants-2014_02
ORD IDord-87197779fa3a49caabdcb9286e3c4e28
Source noteuspto-grants-2014_02