Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801048Generated: October 31, 2026

Potassium Hydroxide → HCID 67440892, compound

https://huagongshe.com/reaction/1801048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-IsopropylpiperazineHCID 78013—
ReactantL-ProlineHCID 145742—
ReactantHCID 67441305HCID 67441305—
CatalystCopper(1+)HCID 104815—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 67440892HCID 6744089299.2%

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), 1-isopropyl piperazine (0.64 g, 5.0 mmol), copper (I) iodidie (120 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-(4-isopropyl-piperazin-1-yl)-phenyl]-3,3-dimethyl-1,2,3,4-tetrahydro-quinoline-6-carboxylic acid ethyl ester (0.27 g, 60%) as a white solid: LC/MS m/e calcd for C27H36FN3O2 (M+H)+: 454.6, observed: 454.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344137B2
Source datasetuspto-grants-2013_01
ORD IDord-ce7c9cad240746768c51952252f5b845
Source noteuspto-grants-2013_01