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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 23736생성일: 2026년 10월 23일

1-Iodopentane → N-benzyl-N'-[3,5-bis(trifluoromethyl)benzoyl]-N-({4-[(pentyloxy)methyl]cyclohexyl}methyl)sulfamide

https://huagongshe.com/ko/reaction/23736

반응식

참여 물질

역할이름HCID투입량
반응물1-IodopentaneHCID 12335—
반응물2,6-Di-tert-butylpyridineHCID 68510—
반응물N-benzyl-N'-[3,5-bis(trifluoromethyl)benzoyl]-N-{[4-(hydroxymethyl)cyclohexyl]methyl}sulfamideHCID 22574483—
촉매Silver(I) trifluoromethanesulfonateHCID 76223—
용매DichloromethaneHCID 6344—
생성물N-benzyl-N'-[3,5-bis(trifluoromethyl)benzoyl]-N-({4-[(pentyloxy)methyl]cyclohexyl}methyl)sulfamideHCID 2257447873.9%

반응 단계

Intermediate (4) (27.6 mg, 50 μmole, 1.0 eq) was dissolved in dichloromethane (250 μL), after which 2,6-di-t-butyl pyridine (36 μL, 160 μmole, 3.2 eq), silver triflate (38.5 mg, 150 μmole, 3.0 eq) and iodopentane (23 μL, 175 μmole, 3.5 eq) were added. After 45 minutes the reaction mixture was directly purified to give 23 mg of the title compound. 1H NMR (500 MHz, DMSO-d6): δ 8.45 (s, 2H), 8.15 (s, 1H), 7.36 (d, 2H), 7.24 (t, 2H), 7.17 (t, 1H), 4.39 (s, 2H), 3.30 (water), 3.23 (t, 2H), 3.01 (d, 2H), 2.92 (d, 2H), 2.48 (DMSO), 1.61 (m, 2H), 1.54 (m, 2H), 1.41 (m, 2H), 1.34-1.19 (m, 6H), 0.82 (t, 3H), 0.62 (m, 4H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06852738B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-a8255898e3c043f2be177310735149d0
출처 메모uspto-grants-2005_02