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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497754Generated: October 25, 2026

Pyridine → 6-Bromo-2,7-dimethyl-8-(3-trifluoromethyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridine

https://huagongshe.com/reaction/1497754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactanthydroxylamine-O-sulfonic acidHCID 76284—
Reactant1,1-Dimethoxyethyl(dimethyl)amineHCID 87835—
Reactant5-Bromo-4-methyl-3-(3-trifluoromethyl-phenyl)-pyridin-2-ylamineHCID 86708086—
SolventDimethylformamideHCID 6228—
Product6-Bromo-2,7-dimethyl-8-(3-trifluoromethyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridineHCID 8670809328.9%

Reaction Conditions

Temperature130 °C

Reaction Steps

To a stirred solution of 5-bromo-4-methyl-3-(3-trifluoromethyl-phenyl)-pyridin-2-ylamine (Int. 1, 1.0 g, 3.02 mmol) in DMF (5 mL) was added dimethylacetamide dimethyl acetal (1.33 mL, 9.06 mmol) and the reaction mixture was heated at 130° C. for 3 hrs. The reaction mixture was cooled then concentrated in vacuo. The resultant residue was dissolved in MeOH (10 mL) and pyridine (486 μL, 6.04 mmol) was added before the mixture was cooled to 0° C. and hydroxylamine-O-sulfonic acid (512 mg, 4.53 mmol) was added. The reaction mixture was allowed to warm to RT and stirred at this temperature for 20 hrs. The resultant precipitate was collected by filtration, then washed with MeOH to afford the title compound as a grey solid (323 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199984B2
Source datasetuspto-grants-2015_12
ORD IDord-32883b72d4974a43b7719206b20b7947
Source noteuspto-grants-2015_12