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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4087생성일: 2026년 10월 23일

1,2,3,4-Tetrahydroquinoline → 10-methyl-7-(4-methyl-1-piperazinyl)-2,3-dihydro-1H-quino[1,8-ab][1,5]benzodiazepine

https://huagongshe.com/ko/reaction/4087

반응식

참여 물질

역할이름HCID투입량
반응물1,2,3,4-TetrahydroquinolineHCID 69460—
반응물4-Fluoro-3-nitrotolueneHCID 136287—
반응물N-[2-(2,3-dihydro-1H-indol-1-yl)-5-fluorophenyl]-4-methyl-1-piperazine carboxamide maleateHCID 70406853—
생성물10-methyl-7-(4-methyl-1-piperazinyl)-2,3-dihydro-1H-quino[1,8-ab][1,5]benzodiazepineHCID 20129109—
생성물1-(4-Methyl-2-nitrophenyl)-1,2,3,4-tetrahydroquinolineHCID 21297653—
생성물2-[3,4-Dihydro-1(2H)-quinolinyl]-5-methylanilineHCID 21297677—

반응 단계

Starting with 1,2,3,4-tetrahydroquinoline and 2-fluoro-5-methylnitrobenzene and following the steps of 1a to 1f of Example 2, one may obtain, in sequence, 1-(4-methyl-2-nitrophenyl)-1,2,3,4-tetrahydroquinoline, 1-(2-amino-4-methylphenyl)-1,2,3,4-tetrahydroquinone, 1-(2-amino-4-methylphenyl)-1,2,3,4-tetrahydroquinoline, N-[2-{1-(5-methylphenyl)-1,2,3,4-tetrahydroquinolin-1-yl}]-4-methyl-1-piperazine carboxamide, and 10-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-3262cb51b9624327bd0dd8061914aac7
출처 메모uspto-grants-1988_02