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HRID 34374作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/34374

反応式

関与物質

役割名称HCID仕込み量
反応物1,2,3,4-TetrahydroquinolineHCID 69460—
反応物4-Bromo-1-fluoro-2-nitrobenzeneHCID 2736328—
反応物9-Flouro-6-(4-methyl-1-piperazinyl)-1,2-dihydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepineHCID 13823288—
生成物1-(4-Bromo-2-nitrophenyl)-1,2,3,4-tetrahydroquinolineHCID 13812927—
生成物5-Bromo-2-[3,4-dihydro-1(2H)-quinolinyl]anilineHCID 13812931—
生成物10-bromo-7-(4-methyl-1-piperazinyl)-2,3-dihydro-1H-quino[1,8-ab][1,5]benzodiazepineHCID 13812943—

反応手順

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-tetrahydro-quinolin-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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04761412
出典データセットuspto-grants-1988_08
ORD IDord-0757bb5dad3945569ca85fc707fb05cd
出典メモuspto-grants-1988_08