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HRID 336394作成日:2026年10月26日

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

https://huagongshe.com/reaction/336394

反応式

関与物質

役割名称HCID仕込み量
反応物3-Isopropylbenzeneboronic acidHCID 2773478—
反応物5-Bromo-[1,2,4]triazolo[1,5-a]pyridin-2-amineHCID 25215939—
触媒HCID 178418476HCID 178418476—
溶媒AcetonitrileHCID 6342—
溶媒Sodium CarbonateHCID 10340—
生成物5-[3-(Propan-2-yl)phenyl][1,2,4]triazolo[1,5-a]pyridin-2-amineHCID 4455611863%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08889673B2
出典データセットuspto-grants-2014_11
ORD IDord-e96686d22c2c4268878fffee847229b6
出典メモuspto-grants-2014_11