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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2045330Generated: October 30, 2026

2-Pyrrolidone → HCID 67441184, compound

https://huagongshe.com/reaction/2045330

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PyrrolidoneHCID 12025—
ReactantPotassium HydroxideHCID 14797—
ReactantAmmonium ChlorideHCID 25517—
ReactantL-ProlineHCID 145742—
ReactantHCID 67441305HCID 67441305—
CatalystCopper(1+)HCID 104815—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 67441184HCID 67441184101.5%

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), pyrrolidin-2-one (0.24 g, 3.0 mmol), copper (I) iodidie (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)(20% ethyl acetate/hexanes) to afford 2-[3-fluoro-5-(2-oxo-pyrrolidin-1-yl)-phenyl]-3,3-dimethyl-1,2,3,4-tetrahydro-quinoline-6-carboxylic acid ethyl ester (0.25 g, 61%) as a white solid: LC/MS m/e calcd for C24H27FN2O3 (M+H)+: 411.5, observed: 411.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586747B2
Source datasetuspto-grants-2013_11
ORD IDord-db6b9caa409b47229854a32c3b673610
Source noteuspto-grants-2013_11