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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4084생성일: 2026년 10월 24일

6-Methyl-1,2,3,4-tetrahydroquinoline → 6-Methyl-1-(2-nitrophenyl)-1,2,3,4-tetrahydroquinoline

https://huagongshe.com/ko/reaction/4084

반응식

참여 물질

역할이름HCID투입량
반응물6-Methyl-1,2,3,4-tetrahydroquinolineHCID 66678—
반응물1-Fluoro-2-nitrobenzeneHCID 73895—
반응물N-[2-(2,3-dihydro-1H-indol-1-yl)-5-fluorophenyl]-4-methyl-1-piperazine carboxamide maleateHCID 70406853—
생성물6-Methyl-1-(2-nitrophenyl)-1,2,3,4-tetrahydroquinolineHCID 21297656—
생성물1-(2-Aminophenyl)-6-methyl-1,2,3,4-tetra-hydroquinolineHCID 21299250—
생성물5-methyl-7-(4-methyl-1-piperazinyl)-2,3-dihydro-1H-quino[1,8-ab][1,5]-benzodiazepineHCID 21299254—

반응 단계

Starting with 6-methyl-1,2,3,4-tetrahydroquinoline and 2-fluoronitrobenzene and following steps 1a to 1f of Example 2, one may obtain, in sequence, 6-methyl-1-(2-nitrophenyl)-1,2,3,4-tetrahydroquinoline, 1-(2-aminophenyl)-6-methyl-1,2,3,4-tetrahydroquinoline, N-[2-(6-methyl-1-phenyl)-1,2,3,4-tetrahydroquinolin-1-yl]-4-methyl-1-piperazine carboxamide, and 5-methyl-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-804949ae43174ef7bf8cecd9db4b4a69
출처 메모uspto-grants-1988_02