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HRID 44204作成日:2026年10月25日

Nitrogen → 4-Chloro-N-(3-chloro-quinoxalin-2-yl)-benzenesulfonamide

https://huagongshe.com/reaction/44204

反応式

関与物質

役割名称HCID仕込み量
反応物NitrogenHCID 947—
反応物Potassium CarbonateHCID 11430—
反応物2,3-DichloroquinoxalineHCID 16659—
反応物4-ChlorobenzenesulfonamideHCID 66824—
溶媒DimethylformamideHCID 6228—
生成物4-Chloro-N-(3-chloro-quinoxalin-2-yl)-benzenesulfonamideHCID 2366510—

反応手順

To a solution of 4-Chlorobenzenesulfonamide (1.92 g, 10 mmol) in anhydrous DMF (50 mL) was added solid potassium carbonate (1.38 g, 10 mmol) in one portion. The reaction mixture was stirred for 10 minutes, followed by the addition of 2,3-dichloroquinoxaline (1.99 g, 10 mmol). Heating the resultant mixture under refux conditions in an atmosphere of N2 for 2.5 h gave the desired product. The progress of the reaction was monitored by TLC using, hexanes/EtOAc 3:1. After cooling the reaction mixture is slowly added to a vigorously stirred aqueous solution of AcOH (1%, 500 mL). The desired product precipitates as grey crystals, which are filtered and dried overnight in desiccator. Yield 2.32 g, 66%; Rf=0.7 (hexanes/EtOAc 1:1); HPLC/MS: [M+H]+ m/z 354. 1H NMR: (DMSO-d6, 600 MHz) 7.68 (t, J=7.8 Hz, 1H), 7.72 (d, J=8.4 Hz, 2H), 7.78 (td, J=7.8 Hz, J=1.2 Hz, 1H), 7.89 (d, J=8.4 Hz, 2H), 8.19 (d, J=8.4 Hz, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541415B2
出典データセットuspto-grants-2013_09
ORD IDord-668aa4d5580442bc9eb04a23c849f206
出典メモuspto-grants-2013_09