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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 276047생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/276047

반응식

참여 물질

역할이름HCID투입량
반응물4-NitrobenzenesulfonamideHCID 22784—
반응물6-Carboxy-1-(2-Chlorobenzyl)-2-MethylbenzimidazoleHCID 18680817—
반응물3-(Cycloundecen-1-yl)-1,2-diazacycloundec-2-eneHCID 53630274—
용매DimethylformamideHCID 6228—
생성물1-(2-Chlorobenzyl)-2-methyl-6-(4-nitrobenzenesulfonylcarbamoyl)benzimidazoleHCID 1868100346.5%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06352985B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-042b19705b0240928c7c3cd9ee2ac19d
출처 메모uspto-grants-2002_03