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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 336394Generated: October 26, 2026

3-Isopropylbenzeneboronic acid → 5-[3-(Propan-2-yl)phenyl][1,2,4]triazolo[1,5-a]pyridin-2-amine

https://huagongshe.com/reaction/336394

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Isopropylbenzeneboronic acidHCID 2773478—
Reactant5-Bromo-[1,2,4]triazolo[1,5-a]pyridin-2-amineHCID 25215939—
CatalystHCID 178418476HCID 178418476—
SolventAcetonitrileHCID 6342—
SolventSodium CarbonateHCID 10340—
Product5-[3-(Propan-2-yl)phenyl][1,2,4]triazolo[1,5-a]pyridin-2-amineHCID 4455611863%

Reaction Steps

A biphasic solution of 5-bromo[1,2,4]triazolo[1,5-a]pyridin-2-amine (0.800 g, 3.76 mmol, 1.00 equiv), 3-(2-propyl)phenyl boronic acid (0.739 g, 4.51 mmol, 1.20 equiv), bis(triphenylphosphine)palladium(II) chloride (0.264 g, 0.376 mmol, 0.100 equiv) in acetonitrile (6 mL) and 1.0M sodium carbonate aqueous solution (6 mL) was heated in the microwave to 160° C. for 2 min. The reaction mixture was partitioned between saturated aqueous sodium chloride solution (10 mL) and ethyl acetate (20 mL). The collected organic was dried over anhydrous magnesium sulfate, filtered, and concentrated. Purification by flash column chromatography (2.5% methanol in dichoromethane) afforded product as a sticky solid (567 mg, 63%). 1H NMR (500 MHz, CDCl3), δ: 7.74 (m, 1H), 7.68 (m, 1H), 7.36-7.48 (m, 4H), 6.79 (dd, J=7.2, 1.3 Hz, 1H), 4.46 (br s, 2H), 3.01 (m, 1H), 1.31 (d, J=6.9 Hz, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889673B2
Source datasetuspto-grants-2014_11
ORD IDord-e96686d22c2c4268878fffee847229b6
Source noteuspto-grants-2014_11