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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 992649Generated: October 30, 2026

Azobisisobutyronitrile → HCID 18412419, compound

https://huagongshe.com/reaction/992649

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
Reactant4-AminobenzonitrileHCID 13396—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 18412597HCID 18412597—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 18412419HCID 18412419—

Reaction Steps

3.5 g (8 mmol) of 1-tert.butoxycarbonyl-2-methyl-indol-5-yl-carboxylic acid-N-phenyl-N-(2-methoxycarbonylethyl)-amide were dissolved in 80 ml of carbon tetrachloride, mixed with 1.5 g (8.4 mmol) of N-bromo-succinimide and 20 mg of azobisisobutyronitrile and refluxed for 2.5 hours. Then the still warm solution was filtered, the filtrate obtained was washed with saturated sodium hydrogen carbonate solution and dried with sodium sulphate. After distillation of the solvent the crude product was dissolved in 30 ml of N-ethyl-diisopropylamine, mixed with 1.0 g (8 mmol) of 4-aminobenzonitrile and refluxed for 2.5 hours. The solvent was distilled off in vacuo and the residue obtained was purified by chromatography (silica gel; ethyl acetate/petroleum ether=1:4 to 1:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06469039B1
Source datasetuspto-grants-2002_10
ORD IDord-ced7311d18ea43b1b285045beaa3b13e
Source noteuspto-grants-2002_10