Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054340Generated: October 26, 2026

Dimethylacetamide → 5-(4-Methoxyphenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-amine

https://huagongshe.com/reaction/1054340

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylacetamideHCID 31374—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant(4-Methoxyphenyl)boronic acidHCID 201262—
Reactant5-Bromo-[1,2,4]triazolo[1,5-a]pyridin-2-amineHCID 25215939—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Product5-(4-Methoxyphenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-amineHCID 59186418—

Reaction Conditions

Temperature150 °C

Reaction Steps

5-Bromo-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine (2 g, 9.4 mmol), 4-methoxybenzeneboronic acid (1.71 g, 11.26 mmol), potassium phosphate (3.98 g, 18.77 mmol) and tetrakis(triphenylphosphine)palladium (0.54 g, 0.47 mmol) were added to a microwave tube containing a stirrer bar. Dimethylacetamide (12 mL) and water (4 mL) were then added and the reaction was heated to 150° C. for 10 min. The reaction was filtered through silica and washed through with methanol and concentrated under reduced pressure. The crude was suspended in diethyl ether and the solid collected and was used without further purification. Yield: 1.70 g, 71%; LCMS method: 1, RT: 3.43 min, MI: 241 [M+1]. NMR 1H (DMSO): 3.82 (s, 3H), 6.16 (brs, 2H), 6.96 (d, 1H), 7.06 (d, 2H), 7.29 (d, 1H), 7.46 (t, 1H), 7.92 (d, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394301B2
Source datasetuspto-grants-2016_07
ORD IDord-47d805cfdd114c4b88a92a3b591b1be0
Source noteuspto-grants-2016_07