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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 530359생성일: 2026년 10월 27일

7-chloro-1-methyl-6-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-3,4-dihydro-1H-quinolin-2-one → (rac)-Ethanesulfonic acid [4-(7-chloro-1-methyl-2-oxo-1,2,3,4-tetrahydro-quinolin-6-yl)-5,6,7,8-tetrahydro-isoquinolin-8-yl]-amide

https://huagongshe.com/reaction/530359

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참여 물질

역할이름HCID투입량
반응물7-chloro-1-methyl-6-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-3,4-dihydro-1H-quinolin-2-oneHCID 86679187—
반응물N-(4-Bromo-5,6,7,8-tetrahydro-8-isoquinolinyl)ethanesulfonamideHCID 89458481—
생성물(rac)-Ethanesulfonic acid [4-(7-chloro-1-methyl-2-oxo-1,2,3,4-tetrahydro-quinolin-6-yl)-5,6,7,8-tetrahydro-isoquinolin-8-yl]-amideHCID 7153734440%

반응 단계

In analogy to the procedure described for the preparation of example 28, 7-chloro-1-methyl-6-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-3,4-dihydro-1H-quinolin-2-one (intermediate A-10) and (rac)-ethanesulfonic acid (4-bromo-5,6,7,8-tetrahydro-isoquinolin-8-yl)-amide (intermediate B-4) were used to give the title compound as a white solid in 40% yield. MS: 434.2 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09353081B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-079599df01644f399727cbe3c05a904f
출처 메모uspto-grants-2016_05