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HRID 276043作成日:2026年10月27日

Benzenesulfonamide → 6-Benzenesulfonylcarbamoyl-1-(2-chlorobenzyl)-2-methylbenzimidazole

https://huagongshe.com/reaction/276043

反応式

関与物質

役割名称HCID仕込み量
反応物BenzenesulfonamideHCID 7370—
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6-Benzenesulfonylcarbamoyl-1-(2-chlorobenzyl)-2-methylbenzimidazoleHCID 1793867150.6%

反応手順

N,N′-carbonyldiimidazole (0.973 g) was added to a solution of 0.902 g of 6-carboxy-1-(2-chlorobenzyl)-2-methylbenzimidazole in 20 ml of N,N-dimethylformamide, and the mixture was stirred at room temperature for 1 hour. Subsequently, a solution of 0.943 g of benzenesulfonamide and 0.913 g of diazabicycloundecene in 5 ml of N,N-dimethylformamide was added thereto, and the mixture was stirred at 100° C. for 70 hours. The reaction solution was cooled, and the solvent was distilled off under reduced pressure. Water and chloroform were added to the residue, and 10% hydrochloric acid was added thereto while being stirred until the aqueous layer was acidified. The mixed solution was extracted twice with chloroform. The resulting organic layer was washed with a saturated aqueous solution of sodium hydrogencarbonate, and the solvent was distilled off under reduced pressure. The residue was dissolved in a small amount of chloroform, and ethyl acetate was added to the solution for crystallization. The crystals were separated through filtration, and were dried to give 0.667 g of 6-benzenesulfonylcarbamoyl-1-(2-chlorobenzyl)-2-methylbenzimidazole (163).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06352985B1
出典データセットuspto-grants-2002_03
ORD IDord-ea1883eb1a1345c9966a533520c85d86
出典メモuspto-grants-2002_03