Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 449223Generated: October 25, 2026

3-Nitrophenylboronic Acid → 5-Methyl-7-(3-nitro-phenyl)-benzo[1,2,4]triazin-3-ylamine

https://huagongshe.com/reaction/449223

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Nitrophenylboronic AcidHCID 1677—
ReactantSodium CarbonateHCID 10340—
Reactant7-Bromo-5-methylbenzo[e][1,2,4]triazin-3-amineHCID 24822752—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
Product5-Methyl-7-(3-nitro-phenyl)-benzo[1,2,4]triazin-3-ylamineHCID 5983760773%

Reaction Steps

An oven dried 25 mL round bottom flask was charged with 7-bromo-5-methyl-benzo[1,2,4]triazin-3-ylamine (1.05 g, 4.49 mmol, 1 equiv), 3-Nitro phenyl boronic acid (1.05 g, 6.29 mmol, 1.4 equiv), sodium carbonate (1.9 g, 18 mmol, 4 equiv) and tetrakis(triphenylphosphine) palladium(0) (0.519 g, 0.449 mmol, 0.1 equiv). The reactants were flushed with argon and diluted with ethylene glycol dimethyl ether (6 mL), ethanol (1 mL) and DI water (1 mL). The reaction vessel was outfitted with condenser and refluxed for 2.5 hours. The reaction was cooled to ambient temperature and diluted with water. The resulting precipitate was filtered off, washed thoroughly with water and dried. Brown solids (0.9 g, 73% yield). MS (ESI+): m/z=282.4, LC retention time: 2.77 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481536B2
Source datasetuspto-grants-2013_07
ORD IDord-66af02ed9cb94322b70340b4f316b657
Source noteuspto-grants-2013_07