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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2045319Generated: October 31, 2026

Piperazine → HCID 67442567, compound

https://huagongshe.com/reaction/2045319

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantPotassium HydroxideHCID 14797—
ReactantAmmonium ChlorideHCID 25517—
ReactantL-ProlineHCID 145742—
ReactantHCID 67441305HCID 67441305—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 67442567HCID 6744256772.9%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 2-(3-bromo-5-fluoro-phenyl)-3,3-dimethyl-1,2,3,4-tetrahydro-quinoline-6-carboxylic acid methyl ester (0.41 g, 1.0 mmol), piperazine (0.26 g, 3.0 mmol), copper (I) iodide (110 mg, 0.6 mmol), L-proline (69 mg, 0.6 mmol) and potassium hydroxide (33.6 mg, 0.6 mmol) in DMSO (2 mL) was stirred at 120° C. for 2 hours. Then treated with saturated ammonium chloride (20 mL), extracted with ether (100 mL). After removal of solvent, the residue was purified on flash silica gel chromatography (silica gel from QingDao, 200-300 mesh, glass column from Shanghai SD company)(40% ethyl acetate/hexanes) to afford 2-(3-fluoro-5-piperazin-1-yl-phenyl)-3,3-dimethyl-1,2,3,4-tetrahydro-quinoline-6-carboxylic acid ethyl ester (0.18 g, 43%) as a white solid: LC/MS m/e calcd for C24H30FN3O2 (M+H)+: 412.5, observed: 412.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586747B2
Source datasetuspto-grants-2013_11
ORD IDord-f57275c52f1845609bda3aaec9c37229
Source noteuspto-grants-2013_11