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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1472854생성일: 2026년 10월 27일

Dimethylacetamide → 5-(1-Benzyl-1H-pyrazol-4-yl)-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine

https://huagongshe.com/reaction/1472854

반응식

참여 물질

역할이름HCID투입량
반응물DimethylacetamideHCID 31374—
반응물Potassium Phosphate, TribasicHCID 62657—
반응물1-Benzyl-1H-pyrazole-4-boronic acidHCID 3352881—
반응물5-Bromo-[1,2,4]triazolo[1,5-a]pyridin-2-amineHCID 25215939—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
생성물5-(1-Benzyl-1H-pyrazol-4-yl)-[1,2,4]triazolo[1,5-a]pyridin-2-ylamineHCID 44555694—

반응 조건

온도150 °C

반응 단계

A vial was charged with 5-bromo-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine (2.00 g, 9.39 mmol), 1-benzylpyrazole-4-boronic acid, pinacol ester (3.20 g, 11.3 mmol), potassium phosphate (4.00 g, 18.8 mmol) and tetrakis(triphenylphosphine)palladium (1.10 g, 0.94 mmol). Dimethylacetamide (24 ml) and water (8 ml) were added and the reaction mixture was heated under microwave irradiation to 150° C. for 10 min. The mixture was partitioned between ethyl acetate and water, and the aqueous phase extracted with ethyl acetate. The combined organic phases were washed several times with water, once with brine, dried over magnesium sulfate and concentrated in vacuo. Trituration in the minimum amount of dichloromethane and diethyl ether afforded an orange solid which required no further purification. Yield: 1.82 g, 67%; LCMS method: 2, RT: 2.37 min, MI: 291 [M+1].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09012633B2
출처 데이터셋uspto-grants-2015_04
ORD IDord-ead253a6db184825beda777485bd4165
출처 메모uspto-grants-2015_04