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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 230718생성일: 2026년 10월 24일

Ethanesulfonic acid → n-{2-Tert-butyl-1-[(4,4-difluorocyclohexyl)methyl]-1h-benzimidazol-5-yl}ethanesulfonamide esylate

https://huagongshe.com/ko/reaction/230718

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참여 물질

역할이름HCID투입량
반응물Ethanesulfonic acidHCID 11668—
반응물Ethanesulfonamide, N-(1-((4,4-difluorocyclohexyl)methyl)-2-(1,1-dimethylethyl)-1H-benzimidazol-5-yl)-HCID 11675994—
반응물Methyl iso-butyl ketone ethane sulphonic acidHCID 131727546—
용매Methyl Isobutyl KetoneHCID 7909—
생성물n-{2-Tert-butyl-1-[(4,4-difluorocyclohexyl)methyl]-1h-benzimidazol-5-yl}ethanesulfonamide esylateHCID 1674258785%

반응 단계

N-{2-tert-butyl-1-[(4,4-difluorocyclohexyl)methyl]-1H-benzimidazol-5-yl}ethanesulfonamide (210 mg) was dissolved in methyl iso-butyl ketone (2.1 ml). A solution was made of ethansulphonic acid (43.7 μl) and methyl iso-butyl ketone (1.0 ml). The methyl iso-butyl ketone/ethane sulphonic acid solution was added in a controlled manner over three hours. Thus, initially, to the base solution was added 2×20 μl acid solution. Then after 30 minutes three more additions were made (3×20 μl). Approximately 20 minutes later three additions of 40 μl acid solution was made and after 40 minutes 400 μl was added. Finally, 20 minutes later the remaining amount of acid solution was added. The resulting slurry was left 2.5 days with stirring before it was filtered off and washed with methyl iso-butyl ketone (2×200 μl). The product was dried at 40° C. under vacuum yielding 227 mg crystalline N-{2-tert-butyl-1-[(4,4-difluorocyclohexyl)methyl]-1H-benzimidazol-5-yl}ethanesulfonamide esylate salt. (yield 85%)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07566788B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-6a4f742e715f4a0d93e9f15a5c1ccd9c
출처 메모uspto-grants-2009_07