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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1896021Generated: October 27, 2026

1,10-Phenanthroline → 1-{3-[1-(3-Nitropyridin-2-yl)piperidin-4-ylidene]prop-1-ynyl}pyrrolidin-2-one

https://huagongshe.com/reaction/1896021

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,10-PhenanthrolineHCID 1318—
ReactantPotassium CarbonateHCID 11430—
Reactant2-PyrrolidoneHCID 12025—
Reactant2-[4-(3-Bromoprop-2-ynylidene)piperidin-1-yl]-3-nitropyridineHCID 86762014—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product1-{3-[1-(3-Nitropyridin-2-yl)piperidin-4-ylidene]prop-1-ynyl}pyrrolidin-2-oneHCID 867620151.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of Compound 261a (111 mg, 0.345 mmol), cupric sulphate (11 mg, 0.69 mmol), 1,10-phenantroline (24.9 mg, 0.138 mmol), K2CO3 (95.4 mg, 0.69 mmol), 2-pyrrolidone (39.7 μl, 0.518 mmol) and 5 mL of toluene was stirred at 80° C. for 12 h. The reaction mixture was cooled to r.t., diluted with EtOAc, washed with water, dried over Na2SO4 and evaporated to dryness in vacuo. The crude residue was purified by automated flash liquid chromatography (Horizon™-Biotage) eluting with PE-EtOAc gradient from 98:2 to 0:10, giving the title product (2 mg)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518916B2
Source datasetuspto-grants-2013_08
ORD IDord-bde8a51850e041a696718e8f14823a94
Source noteuspto-grants-2013_08