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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2045925Generated: October 31, 2026

1-Phenylpiperazine → HCID 3759112, compound

https://huagongshe.com/reaction/2045925

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PhenylpiperazineHCID 7096—
ReactantPotassium CarbonateHCID 11430—
Reactant18-Crown-6HCID 28557—
Reactant2-chloro-N-(3-quinoxalin-2-ylphenyl)acetamideHCID 1485433—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 3759112HCID 375911290.2%

Reaction Steps

A slurry of 2-chloro-N-(3-quinoxalin-2-ylphenyl)acetamide (1.64 g, 5.5 mmol), K2CO3 (0.92 g, 6.87 mmol), 1-phenylpiperazine (1.05 mL, 5.5 mmol) and a catalytical amount of 18-crown-6 in MeCN (20 mL) was refluxed for 7 hrs, cooled to room temperature, and diluted with water. The resulting solid was filtered, washed with water, and dried to afford 2-(4-phenylpiperazin-1-yl)-N-[3-(quinoxalin-2-yl)phenyl]acetamide (2.1 g, 90% yield). LCMS calculated for C26H25N50 (M+H): 424.52. found 424. 1H-NMR (DMSO-d6, 250 Mhz) δH: 10.5 (1H, br. s), 9.52 (1H, s), 8.58 (1H, br. s), 8.20-7.80 (6H, m), 7.55 (1H, m), 7.25-7.15 (2H, m), 6.98-6.90 (2H, m), 6.80-6.72 (1H, m), 3.28-3.25 (6H, m), 2.75-2.65 (4H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592415B2
Source datasetuspto-grants-2013_11
ORD IDord-a865c17a209b4ef6b328faf0df6cb803
Source noteuspto-grants-2013_11