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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2195539Generated: October 30, 2026

Azobisisobutyronitrile → HCID 66767297, compound

https://huagongshe.com/reaction/2195539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantMorpholineHCID 8083—
ReactantPotassium CarbonateHCID 11430—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 58158591HCID 58158591—
SolventMethanolHCID 887—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 66767297HCID 6676729747.2%

Reaction Steps

A mixture of ethyl 1-(4-fluorophenyl)-5-methyl-2-oxo-1,2-dihydropyridine-3-carboxylate (0.275 g, 1 mmol), NBS (0.2 g, 1.1 mmol), AIBN (40 mg, 0.2 mmol) in CCl4 (20 mL) is heated at reflux for 3 hours. After the reaction is cooled down, morpholine (0.088 mL, 1 mmol) and K2CO3 (0.14 g, 1 mmol) are added. The reaction is stirred at RT for another 2 hours. The solvent is removed, and the residue is diluted with water (10 mL) and extracted with EtOAc (20 mL) twice. The combined organic phases are washed with saturated aqueous sodium chloride, dried, and concentrated. The residue is purified by silica gel column chromatography eluting with DCM:MeOH (from 100:1 to 50:1, containing 0.5% 2 N NH3 in MeOH), to afford the title compound (0.17 g, 47% yield). MS (m/z): 361.1 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE043878E1
Source datasetuspto-grants-2012_12
ORD IDord-938257a1f5a04a02bbaf1cf481099101
Source noteuspto-grants-2012_12