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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1272476Generated: October 25, 2026

Potassium Carbonate → [7-(2-Fluoro-6-methoxy-phenyl)-5-methyl-benzo[1,2,4]triazin-3-yl]-phenyl-amine

https://huagongshe.com/reaction/1272476

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTriphenylphosphineHCID 11776—
Reactant(2-Fluoro-6-methoxyphenyl)boronic acidHCID 3294524—
Reactant(7-Bromo-5-methyl-benzo[1,2,4]triazin-3-yl)-phenyl-amineHCID 18455767—
CatalystTris(dibenzylideneacetone) dipalladiumHCID 9832798—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDimethylacetamideHCID 31374—
Product[7-(2-Fluoro-6-methoxy-phenyl)-5-methyl-benzo[1,2,4]triazin-3-yl]-phenyl-amineHCID 1845575817.5%

Reaction Steps

To a solution of (7-Bromo-5-methyl-benzo[1,2,4]triazin-3-yl)-phenyl-amine (10 mg, 0.032 mmol) dissolved in 2 ml N,N-Dimethylacetamide in a 20 ml vial, 2-Fluoro-6-methoxy-phenylboronic acid (22 mg, 0.128 mmol) dissolved in 1 ml ethanol and potassium carbonate (6.4 mg, 0.06 mmol) dissolved in 1 ml water were added. Triphenylphosphine (1 mg, 0.0038 mmol) and tris(dibenzylideneacetone) dipalladium (0) (1 mg, 1.09 umol) were added to the mixture. The mixture was reflux overnight. The crude product was filtered and purified by preparative HPLC. 2 mg [7-(2-Fluoro-6-methoxy-phenyl)-5-methyl-benzo[1,2,4]triazin-3-yl]-phenyl-amine was isolated. Yield: 17.5%; ESI-MS: [M+H]+, 361; 1H NMR (CDCl3): δ 2.73 (s, 3 H), 3.83 (s, 3 H), 6.83–6.86 (m, 2H), 7.14 (m, 1 H), 7.34 (m, 1 H), 7.45 (m, 2 H), 7.75(s, 1 H), 7.92(m, 2 H), 8.24(s, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07208493B2
Source datasetuspto-grants-2007_04
ORD IDord-ee7907328a164a9ea2b5e8dae5fbd579
Source noteuspto-grants-2007_04