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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1992469생성일: 2026년 10월 26일

2-Chloropyridine-4-boronic acid → (4-Benzenesulfonyl-piperazin-1-yl)-[1-(2-chloro-pyridin-4-yl)-5-(4-isopropyl-piperazine-1-carbonyl)-1H-indol-2-yl]-methanone

https://huagongshe.com/reaction/1992469

반응식

참여 물질

역할이름HCID투입량
반응물2-Chloropyridine-4-boronic acidHCID 5151595—
반응물(4-Benzenesulfonyl-piperazin-1-yl)-[5-(4-isopropyl-piperazine-1-carbonyl)-1H-indol-2-yl]-methanoneHCID 68535846—
생성물(4-Benzenesulfonyl-piperazin-1-yl)-[1-(2-chloro-pyridin-4-yl)-5-(4-isopropyl-piperazine-1-carbonyl)-1H-indol-2-yl]-methanoneHCID 8662192944%

반응 단계

The title compound was synthesized in analogy to example 5, from (4-benzenesulfonyl-piperazin-1-yl)-[5-(4-isopropyl-piperazine-1-carbonyl)-1H-indol-2-yl]-methanone (example 13) and 2-chloropyridine-4-boronic acid to afford the desired product as a light brown solid (44%). MS (ISP): 635.3 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07648979B2
출처 데이터셋uspto-grants-2010_01
ORD IDord-3dacbe03a7284767bd6908733d05b419
출처 메모uspto-grants-2010_01