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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4085생성일: 2026년 10월 23일

1,2,3,4-Tetrahydroquinoline → 1-(4-Bromo-2-nitrophenyl)-1,2,3,4-tetrahydroquinoline

https://huagongshe.com/ko/reaction/4085

반응식

참여 물질

역할이름HCID투입량
반응물1,2,3,4-TetrahydroquinolineHCID 69460—
반응물4-Bromo-1-fluoro-2-nitrobenzeneHCID 2736328—
반응물N-[2-(2,3-dihydro-1H-indol-1-yl)-5-fluorophenyl]-4-methyl-1-piperazine carboxamide maleateHCID 70406853—
생성물1-(4-Bromo-2-nitrophenyl)-1,2,3,4-tetrahydroquinolineHCID 13812927—
생성물5-Bromo-2-[3,4-dihydro-1(2H)-quinolinyl]anilineHCID 13812931—
생성물10-bromo-7-(4-methyl-1-piperazinyl)-2,3-dihydro-1H-quino[1,8-ab][1,5]benzodiazepineHCID 13812943—

반응 단계

Starting with 1,2,3,4-tetrahydroquinoline and 5-bromo-2-fluoronitrobenzene and following the steps of 1a to 1f of Example 2, one may obtain, in sequence, 1-(4-bromo-2-nitrophenyl)-1,2,3,4-tetrahydroquinoline, 1-(2-amino-4-bromophenyl)-1,2,3,4-tetrahydroquinoline, N-[2-{1-(5-bromophenyl)-1,2,3,4-tetrahydroquinolin-1-yl}]-4-methyl-1-piperazine carboxamide, and 10-bromo-7-(4-methyl-1-piperazinyl)-2,3-dihydro-1H-quino[1,8-ab][1,5]benzodiazepine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04723003
출처 데이터셋uspto-grants-1988_02
ORD IDord-f25e2397d0e44ac98f1fbbc579c59523
출처 메모uspto-grants-1988_02