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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1513932생성일: 2026년 10월 26일

2-Bromo-1,3,4-trifluorobenzene → [6-Methoxy-2-(2,3,6-trifluoro-phenyl)-naphthalen-1-yl]-[4-(2-piperidin-1-yl-ethoxy)-phenyl]-methanone

https://huagongshe.com/reaction/1513932

반응식

참여 물질

역할이름HCID투입량
반응물2-Bromo-1,3,4-trifluorobenzeneHCID 2736401—
반응물[6-Hydroxy-2-(2,3,5-trifluoro-phenyl)-naphthalen-1-yl]-[4-(2-piperidin-1-yl-ethoxy)-phenyl]-methanoneHCID 11237470—
반응물Trifluoromethanesulfonic acid 6-methoxy-1-[4-(2-piperidin-1-yl-ethoxy)benzoyl]-naphthalen-2-yl esterHCID 11685250—
생성물[6-Methoxy-2-(2,3,6-trifluoro-phenyl)-naphthalen-1-yl]-[4-(2-piperidin-1-yl-ethoxy)-phenyl]-methanoneHCID 5755252545.1%

반응 단계

Couple trifluoromethanesulfonic acid 6-methoxy-1-[4-(2-piperidin-1-yl-ethoxy)-benzoyl]-naphthalen-2-yl ester (1.81 g, 3.37 mmol) with 2-bromo-1,3,4-trifluoro-benzene (1.42 g, 6.75 mmol) in a procedure similar to the preparation of [6-hydroxy-2-(2,3,5-trifluoro-phenyl)-naphthalen-1-yl]-[4-(2-piperidin-1-yl-ethoxy)-phenyl]-methanone to give 0.79 g (45%) of the title compound: mass spectrum (ion spray): m/z=520.3 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08217032B2
출처 데이터셋uspto-grants-2012_07
ORD IDord-e95c3eed9d834acd87238ef5efe2cae7
출처 메모uspto-grants-2012_07