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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 19864생성일: 2026년 10월 23일

3-Cyanophenylboronic acid → 3-[2-(4,4-Difluoro-piperidine-1-carbonyl)-5-(1-isopropyl-piperidin-4-yloxy)-indol-1-yl]-benzonitrile

https://huagongshe.com/ko/reaction/19864

반응식

참여 물질

역할이름HCID투입량
반응물3-Cyanophenylboronic acidHCID 2734325—
반응물(4,4-Difluoropiperidin-1-yl)[5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]methanoneHCID 11603838—
생성물3-[2-(4,4-Difluoro-piperidine-1-carbonyl)-5-(1-isopropyl-piperidin-4-yloxy)-indol-1-yl]-benzonitrileHCID 16739528—

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 3-cyanophenylboronic acid. The title compound was obtained in 46% yield as yellow foam. MS (m/e): 507.3 (MH+, 100%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745479B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-5002c25decad4be9ae66d0efbe0bb9bb
출처 메모uspto-grants-2010_06