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HRID 537849作成日:2026年10月24日

N-(3-Aminophenyl)-1-phenylmethanesulfonamide → N-(3-((5-(4-cyanophenyl)oxazol-2-yl)amino)phenyl)-1-phenylmethanesulfonamide

https://huagongshe.com/ja/reaction/537849

反応式

関与物質

役割名称HCID仕込み量
反応物N-(3-Aminophenyl)-1-phenylmethanesulfonamideHCID 16772451—
反応物4-(2-Chlorooxazol-5-yl)benzonitrileHCID 68443558—
溶媒IsopropanolHCID 3776—
生成物N-(3-((5-(4-cyanophenyl)oxazol-2-yl)amino)phenyl)-1-phenylmethanesulfonamideHCID 71060644—

反応条件

温度80 °C

反応手順

A mixture of 4-(2-chlorooxazol-5-yl)benzonitrile 2 (0.20 g, 0.98 mmol) and N-(3-aminophenyl)-1-phenylmethanesulfonamide 4 (0.256 g, 0.98 mmol) in 2-propanol (20 mL) was heated to 80° C. for 18 h with stirring. Upon cooling, a white solid precipitated out which was filtered off, washed with 2-propanol, and dried. This was then triturated with ether and filtered to yield the title product, a white solid, as the hydrochloride salt of 5 (0.15 g, 36%). Free amine containing filtrate was evaporated and silica column purified (Biotage) (Acetone/hexane as an eluent) to provide 5 (0.15 g, 36% yield) as pale yellow solid. MS (ES) m/z 431 (M+H+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08865709B2
出典データセットuspto-grants-2014_10
ORD IDord-2c17b9bee21e4cc08df6e108e92c2e04
出典メモuspto-grants-2014_10