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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 336394Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/336394

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Isopropylbenzeneboronic acidHCID 2773478—
Edukt5-Bromo-[1,2,4]triazolo[1,5-a]pyridin-2-amineHCID 25215939—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelAcetonitrileHCID 6342—
LösungsmittelSodium CarbonateHCID 10340—
Produkt5-[3-(Propan-2-yl)phenyl][1,2,4]triazolo[1,5-a]pyridin-2-amineHCID 4455611863%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08889673B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-e96686d22c2c4268878fffee847229b6
Quellennotizuspto-grants-2014_11