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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 19860생성일: 2026년 10월 25일

4-Chlorophenylboronic acid → [1-(4-Chloro-phenyl)-5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-(4,4-difluoro-piperidin-1-yl)-methanone

https://huagongshe.com/reaction/19860

반응식

참여 물질

역할이름HCID투입량
반응물4-Chlorophenylboronic acidHCID 74299—
반응물(4,4-Difluoropiperidin-1-yl)[5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]methanoneHCID 11603838—
생성물[1-(4-Chloro-phenyl)-5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-(4,4-difluoro-piperidin-1-yl)-methanoneHCID 16739484—

반응 단계

In analogy to the procedure described for the synthesis of example 6, the title compound was synthesized from (4,4-difluoro-piperidin-1-yl)-[5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-methanone (intermediate 1) and 4-chlorophenylboronic acid. The title compound was obtained in 93% yield as light yellow foam. MS (m/e): 516.2 (MH+, 100%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745479B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-ed8689e4235245b6a0b86a4fdd4bed96
출처 메모uspto-grants-2010_06