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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1050708Generated: October 29, 2026

Sodium hydride → 4,7-bis(4-(N,N-diphenylamino)phenyl)-2-(6-cyanopyridin-3-yl)-2H-benzo[d][1,2,3]triazole

https://huagongshe.com/reaction/1050708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-Cyano-5-fluoropyridineHCID 11332453—
Reactant4,7-bis(4-(N,N-diphenylamino)phenyl)-2H-benzo[d][1,2,3]triazoleHCID 86679912—
SolventDimethylformamideHCID 6228—
Product4,7-bis(4-(N,N-diphenylamino)phenyl)-2-(6-cyanopyridin-3-yl)-2H-benzo[d][1,2,3]triazoleHCID 86679923—

Reaction Conditions

Temperature80 °C

Reaction Steps

Sodium hydride (60%, 120 mg, 3 mmol) was added to a solution of Intermediate P (1.21 g, 2.0 mmol) and 5-fluoro-2-pyridinecarbonitrile (0.61 g, 5.0 mmol) in anhydrous dimethylformamide (20 mL), stirred under argon, and the obtained mixture was heated at 80° C. for 16 hours. The reaction mixture was poured into ice/water (200 mL), and extracted with dichloromethane (200 mL). The extract was dried over sodium sulfate, and the solvent was evaporated. The residue was diluted with chlorobenzene (50 mL), and the volatiles were removed under high vacuum. The crude product was purified by chromatography (dichloromethane/hexane 2:1) to give 4,7-bis(4-(N,N-diphenylamino)phenyl)-2-(6-cyanopyridin-3-yl)-2H-benzo[d][1,2,3]triazole, dark-red crystals, 1.20 g (85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382424B2
Source datasetuspto-grants-2016_07
ORD IDord-c247e9d7d4ac480bb82b47a1217157c6
Source noteuspto-grants-2016_07