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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 555360생성일: 2026년 10월 26일

Trifluoroacetic acid → (E)-N1-(3-(1H-imidazol-1-yl)propyl)-N8-hydroxy-2-((naphthalen-1-yloxy)methyl)octenediamide

https://huagongshe.com/reaction/555360

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물Dichloromethane methanolHCID 21226129—
반응물(E)-N1-(3-(1H-imidazol-1-yl)propyl)-2-((naphthalen-1-yloxy)methyl)-N8-(tetra hydro-2H-pyran-2-yloxy)-2-octenediamideHCID 86640100—
용매MethanolHCID 887—
생성물(E)-N1-(3-(1H-imidazol-1-yl)propyl)-N8-hydroxy-2-((naphthalen-1-yloxy)methyl)octenediamideHCID 1611744437%

반응 단계

(E)-N1-(3-(1H-imidazol-1-yl)propyl)-2-((naphthalen-1-yloxy)-methyl)-N8-(tetrahydro-2H-pyran-2-yloxy)-2-octenediamide (203 mg, 0.38 mM) obtained in Example (2-1-3) was dissolved in methanol (2 ml), and trifluoroacetic acid (146 μl, 1.90 mM) was slowly added thereto at 0° C. Then, the resulting mixture was heated to room temperature and reacted for 18 hrs. After the completion of reaction, the solvent was removed under reduced pressure. The residue thus obtained was subjected to a silica gel column chromatography (eluent: methanol/dichloromethane=1/9) to obtain 63 mg of the title compound (yield 37%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08053435B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-e28a77b847124935a30960ddb6b8fa2e
출처 메모uspto-grants-2011_11