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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 34375생성일: 2026년 10월 24일

4-Chloro-1-fluoro-2-nitrobenzene → 5-Chloro-2-[3,4-dihydro-1(2H)-quinolinyl]aniline

https://huagongshe.com/ko/reaction/34375

반응식

참여 물질

역할이름HCID투입량
반응물4-Chloro-1-fluoro-2-nitrobenzeneHCID 67660—
반응물1,2,3,4-TetrahydroquinolineHCID 69460—
반응물9-Flouro-6-(4-methyl-1-piperazinyl)-1,2-dihydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepineHCID 13823288—
생성물5-Chloro-2-[3,4-dihydro-1(2H)-quinolinyl]anilineHCID 19624508—
생성물10-chloro-7-(4-methyl-1-piperazinyl)-2,3-dihydro-1H-quino[1,8-ab][1,5]benzodiazepineHCID 20129108—
생성물1-(4-Chloro-2-nitrophenyl)-1,2,3,4-tetrahydroquinolineHCID 21297647—

반응 단계

Starting with 1,2,3,4-tetrahydroquinoline and 5-chloro-2-fluoronitrobenzene and following the steps of 1a to 1f of Example 2, one may obtain, in sequence, 1-(4-chloro-2-nitrophenyl)-1,2,3,4-tetrahydroquinoline, 1-(2-amino-4-chlorophenyl)-1,2,3,4-tetrahydroquinoline, N-[2-{1-(5-chlorophenyl)-1,2,3,4-tetrahydroquinoline-1-yl}]-4-methyl-1-piperazine carboxamide, and 10-chloro-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 번호US04761412
출처 데이터셋uspto-grants-1988_08
ORD IDord-37f9a56e4374462ea8f84b378b5fce66
출처 메모uspto-grants-1988_08