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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethanesulfonic acid | HCID 11668 | — |
| 반응물 | Ethanesulfonamide, N-(1-((4,4-difluorocyclohexyl)methyl)-2-(1,1-dimethylethyl)-1H-benzimidazol-5-yl)- | HCID 11675994 | — |
| 반응물 | Methyl iso-butyl ketone ethane sulphonic acid | HCID 131727546 | — |
| 용매 | Methyl Isobutyl Ketone | HCID 7909 | — |
| 생성물 | n-{2-Tert-butyl-1-[(4,4-difluorocyclohexyl)methyl]-1h-benzimidazol-5-yl}ethanesulfonamide esylate | HCID 16742587 | 85% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07566788B2 |
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| 출처 데이터셋 | uspto-grants-2009_07 |
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| ORD ID | ord-6a4f742e715f4a0d93e9f15a5c1ccd9c |
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| 출처 메모 | uspto-grants-2009_07 |
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