戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1276908作成日:2026年10月27日

4-Nitrobenzenesulfonamide → 1-(2-Chlorobenzyl)-2-methyl-6-(4-nitrobenzenesulfonylcarbamoyl)benzimidazole

https://huagongshe.com/reaction/1276908

反応式

関与物質

役割名称HCID仕込み量
反応物4-NitrobenzenesulfonamideHCID 22784—
反応物6-Carboxy-1-(2-Chlorobenzyl)-2-MethylbenzimidazoleHCID 18680817—
反応物3-(Cycloundecen-1-yl)-1,2-diazacycloundec-2-eneHCID 53630274—
溶媒DimethylformamideHCID 6228—
生成物1-(2-Chlorobenzyl)-2-methyl-6-(4-nitrobenzenesulfonylcarbamoyl)benzimidazoleHCID 1868100346.5%

反応手順

N,N'-carbodiimidazole (0.432 g) was added at a time to a solution of 0.400 g of 6-carboxy-1-(2-chlorobenzyl)-2-methylbenzimidazole in 15 ml of N,N-dimethylformamide, and the solution was stirred at room temperature for 1 hour. Subsequently, a solution of 0.538 g of 4-nitrobenzenesulfonamide and 0.405 g of diazabicycloundecene in 5 ml of N,N-dimethylformamide, and the mixture was stirred at 100° C. for 84 hours. The reaction solution was cooled, and the solvent was distilled off under reduced pressure. Chloroform and hydrochloric acid were added to the residue, and the mixture was stirred to precipitate the crystals. The crystals precipitated were separated through filtration, and were dried to give 0.300 g of 1-(2-chlorobenzyl)-2-methyl-6-(4-nitrobenzenesulfonylcarbamoyl)benzimidazole (220).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06166219
出典データセットuspto-grants-2000_12
ORD IDord-86bedd3ec8fe4d2b909a2f1c6b7011a6
出典メモuspto-grants-2000_12