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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1699618생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1699618

반응식

참여 물질

역할이름HCID투입량
반응물4-NitrobenzenesulfonamideHCID 22784—
반응물6-Carboxy-1-(2-Chlorobenzyl)-2-MethylbenzimidazoleHCID 18680817—
용매DimethylformamideHCID 6228—
생성물1-(2-Chlorobenzyl)-2-methyl-6-(4-nitrobenzenesulfonylcarbamoyl)benzimidazoleHCID 1868100343.1%

반응 단계

N,N′-carbonyldiimidazole (0.432 g) is added all at once to an N,N-dimethylformamide (15 ml) solution of 6-carboxy-1-(2-chlorobenzyl)-2-methylbenzimidazole (0.432 g) (example 75), and the solution is stirred for one hour at room temperature. Subsequently, an N,N-dimethylformamide (5 ml) solution of 4-nitrobenzenesulfonamide (0.538 g) and diazabicyclotindecene (0.405 g) is added, and the solution is stirred for 84 hours at 100° C. The reaction solution is cooled and the solvent is removed through evaporation under reduced pressure. When chloroform and hydrochloric acid are added to the residue and the solution is stirred, crystals precipitated. The crystals are separated through filtration, dried, and thus, 1-(2-chlorobenzyl)-2-methyl-6-(4-nitrobenzenesulfonylcarbamoyl)benzimidazole (0.300 g) is obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06348032B1
출처 데이터셋uspto-grants-2002_02
ORD IDord-08d94b7200534d1ab77db94f0a2fe645
출처 메모uspto-grants-2002_02