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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 336394생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/336394

반응식

참여 물질

역할이름HCID투입량
반응물3-Isopropylbenzeneboronic acidHCID 2773478—
반응물5-Bromo-[1,2,4]triazolo[1,5-a]pyridin-2-amineHCID 25215939—
촉매HCID 178418476HCID 178418476—
용매AcetonitrileHCID 6342—
용매Sodium CarbonateHCID 10340—
생성물5-[3-(Propan-2-yl)phenyl][1,2,4]triazolo[1,5-a]pyridin-2-amineHCID 4455611863%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08889673B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-e96686d22c2c4268878fffee847229b6
출처 메모uspto-grants-2014_11