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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1427826생성일: 2026년 10월 26일

Tricyclo(3.3.1.1'3,7)dec-1-ylmethanol → 5-chloro-N-(N,N-dimethylsulfamoyl)-2-fluoro-4-(spiro[2.5]octan-6-ylmethoxy)benzamide

https://huagongshe.com/reaction/1427826

반응식

참여 물질

역할이름HCID투입량
반응물Tricyclo(3.3.1.1'3,7)dec-1-ylmethanolHCID 64556—
반응물(Spiro(2.5)octan-6-yl)methanolHCID 53487089—
반응물5-chloro-2,4-difluoro-N-(methylsulfonyl)benzamideHCID 58042417—
반응물5-chloro-N-(N,N-dimethylsulfamoyl)-2,4-difluorobenzamideHCID 86702836—
생성물5-chloro-N-(N,N-dimethylsulfamoyl)-2-fluoro-4-(spiro[2.5]octan-6-ylmethoxy)benzamideHCID 86702852—

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 spiro[2.5]octan-6-ylmethanol, the title compound was obtained as a colorless solid (0.17 g, 40%): 1H NMR (300 MHz, CDCl3) δ 8.65-8.59 (m, 1H), 8.06 (d, J=8.1 Hz, 1H), 6.67 (d, J=13.8 Hz, 1H), 3.88 (d, J=6.3 Hz, 2H), 3.01 (s, 6H), 1.95-1.72 (m, 5H), 1.34-1.21 (m, 2H), 0.96-0.90 (m, 2H), 0.33-0.26 (m, 2H), 0.22-0.16 (m, 2H); MS (ES−) m/z: 417.2, 419.2 (M−1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08933236B2
출처 데이터셋uspto-grants-2015_01
ORD IDord-13b2bf1c2f3f4db2b4e7b2a55afdc5ea
출처 메모uspto-grants-2015_01