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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1427842생성일: 2026년 10월 26일

Tricyclo(3.3.1.1'3,7)dec-1-ylmethanol → 5-chloro-4-(cycloheptylmethoxy)-N-(N,N-dimethylsulfamoyl)-2-fluorobenzamide

https://huagongshe.com/reaction/1427842

반응식

참여 물질

역할이름HCID투입량
반응물Tricyclo(3.3.1.1'3,7)dec-1-ylmethanolHCID 64556—
반응물CycloheptanemethanolHCID 78193—
반응물5-chloro-2,4-difluoro-N-(methylsulfonyl)benzamideHCID 58042417—
반응물5-chloro-N-(N,N-dimethylsulfamoyl)-2,4-difluorobenzamideHCID 86702836—
생성물5-chloro-4-(cycloheptylmethoxy)-N-(N,N-dimethylsulfamoyl)-2-fluorobenzamideHCID 86702869—

반응 단계

Following the procedure as described in Example 8 and making variations as required to replace 5-chloro-2,4-difluoro-N-(methylsulfonyl)benzamide with 5-chloro-N—(N,N-dimethylsulfamoyl)-2,4-difluorobenzamide and adamantan-1-ylmethanol with cycloheptylmethanol, the title compound was obtained as a colorless solid (0.08 g, 20%): 1H NMR (300 MHz, DMSO-d6) δ 11.77 (s, 1H), 7.72 (d, J=7.4 Hz, 1H), 7.24 (d, J=12.3 Hz, 1H), 3.94 (d, J=6.6 Hz, 2H), 2.87 (s, 6H), 2.00-1.25 (m, 13H); MS (ES−) m/z 405.1, 407.1 (M−1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08933236B2
출처 데이터셋uspto-grants-2015_01
ORD IDord-427daaec43d54737801b3ac43bec2626
출처 메모uspto-grants-2015_01