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HRID 383660作成日:2026年10月25日

3-(2-Methyl-1H-imidazol-1-yl)aniline → 5-(3-(2-methyl-1H-imidazol-1-yl)phenylamino)pyrazolo[1,5-a]pyrimidine-3-carbaldehyde

https://huagongshe.com/reaction/383660

反応式

関与物質

役割名称HCID仕込み量
反応物3-(2-Methyl-1H-imidazol-1-yl)anilineHCID 12797139—
反応物5-Chloropyrazolo(1,5-a)pyrimidine-3-carbaldehydeHCID 58196401—
溶媒1,4-DioxaneHCID 31275—
生成物5-(3-(2-methyl-1H-imidazol-1-yl)phenylamino)pyrazolo[1,5-a]pyrimidine-3-carbaldehydeHCID 5819675770.1%

反応条件

温度120 °C

反応手順

To 5-chloropyrazolo[1,5-a]pyrimidine-3-carbaldehyde (39 mg, 0.215 mmol) in dioxane was added 3-(2-methyl-1H-imidazol-1-yl)aniline (90 mg, 0.520 mmol). The mixture was heated in microwave (200 W) for 50 minutes at 120° C. The solid formed was isolated by filtration and air dried to yield 48 mg 5-(3-(2-methyl-1H-imidazol-1-yl)phenylamino)pyrazolo[1,5-a]pyrimidine-3-carbaldehyde (70% yield). LCMS (M+1=319)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08367681B2
出典データセットuspto-grants-2013_02
ORD IDord-0fb720464be444f1a2d628ab5898e849
出典メモuspto-grants-2013_02