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HRID 39159作成日:2026年10月23日

Water → 3'-amino-N-methylbiphenyl-4-sulfonamide

https://huagongshe.com/ja/reaction/39159

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Potassium CarbonateHCID 11430—
反応物3-Aminophenylboronic acidHCID 92269—
反応物4-bromo-N-methylbenzene-1-sulfonamideHCID 101215—
触媒HCID 178418397HCID 178418397—
溶媒DimethylformamideHCID 6228—
生成物3'-amino-N-methylbiphenyl-4-sulfonamideHCID 5920619150%

反応条件

温度80 °C

反応手順

To a solution of 4-bromo-N-methyl-benzene sulfonamide (2.49 g, 10 mmol) in DMF (20 mL) was added 3-amino-phenyl boronic acid (1.51 g, 11 mmol), Pd(PPh3)4 (90 mg, 0.30 mmol), potassium carbonate (1.52 g, 11 mmol) and water (5 mL). The resulting mixture was degassed by gently bubbling argon through the solution for 5 minutes at 20° C. The reaction mixture was then heated at 80° C. overnight. The reaction was filtered through a pad of silica gel, which was washed with CH2Cl2 (50 mL×3). The combined organics were concentrated under reduced pressure to give crude product, which was washed with EtOAc to give pure 3′-amino-N-methylbiphenyl-4-sulfonamide (C-3) (1.3 g, 50%). NMR (300 MHz, CDCl3) δ 7.85 (d, J=8.7 Hz, 2H), 7.75 (d, J=8.7 Hz, 2H), 7.19 (t, J=7.8 Hz, 1H), 6.95-7.01 (m 2H), 6.73-6.77 (m, 1H), 2.54 (s, 3H). MS (ESI) m/e (M+H+) 263.0.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524767B2
出典データセットuspto-grants-2013_09
ORD IDord-c4df9bd19f31462292cf31d960a25ce6
出典メモuspto-grants-2013_09