戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1472854作成日:2026年10月27日

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

https://huagongshe.com/reaction/1472854

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylacetamideHCID 31374—
反応物Potassium Phosphate, TribasicHCID 62657—
反応物1-Benzyl-1H-pyrazole-4-boronic acidHCID 3352881—
反応物5-Bromo-[1,2,4]triazolo[1,5-a]pyridin-2-amineHCID 25215939—
触媒HCID 178418397HCID 178418397—
溶媒WaterHCID 962—
生成物5-(1-Benzyl-1H-pyrazol-4-yl)-[1,2,4]triazolo[1,5-a]pyridin-2-ylamineHCID 44555694—

反応条件

温度150 °C

反応手順

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].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09012633B2
出典データセットuspto-grants-2015_04
ORD IDord-ead253a6db184825beda777485bd4165
出典メモuspto-grants-2015_04