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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1072934생성일: 2026년 10월 25일

1-Butanesulfonamide → 6-(1-n-Butanesulfonylcarbamoyl)-1-(2,4-dichlorobenzyl)-3-methyl-2-benzimidazolone

https://huagongshe.com/reaction/1072934

반응식

참여 물질

역할이름HCID투입량
반응물1-ButanesulfonamideHCID 18460—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물6-Carboxy-1-(2,4-dichlorobenzyl)-3-methyl-2-benzimidazoloneHCID 22387851—
용매DimethylformamideHCID 6228—
생성물6-(1-n-Butanesulfonylcarbamoyl)-1-(2,4-dichlorobenzyl)-3-methyl-2-benzimidazoloneHCID 2238775729.2%

반응 단계

In the same manner as in Example 1, N,N′-carbonyldiimidazole (0.290 g) was added to a mixture of 6-carboxy-1-(2,4-dichlorobenzyl)-3-methyl-2-benzimidazolone (0.314 g) and N,N-dimethylformamide (9 ml), and the mixture was stirred at room temperature for 1 hr. 1-n-Butanesulfonamide (0.246 g) and DBU (0.273 g) were added and the mixture was stirred at 100° C. for 16 hr. The solvent was evaporated and the resulting mixture was extracted with chloroform and water. The organic layer was concentrated and the residue was purified by preparative thin layer chromatography to give 6-(1-n-butanesulfonylcarbamoyl)-1-(2,4-dichlorobenzyl)-3-methyl-2-benzimidazolone (0.123 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06911469B2
출처 데이터셋uspto-grants-2005_06
ORD IDord-8b93bcaac0704066b3b7b120e0d3fb05
출처 메모uspto-grants-2005_06