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HRID 34373作成日:2026年10月26日

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

https://huagongshe.com/reaction/34373

反応式

関与物質

役割名称HCID仕込み量
反応物6-Methyl-1,2,3,4-tetrahydroquinolineHCID 66678—
反応物1-Fluoro-2-nitrobenzeneHCID 73895—
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6-Methyl-1-(2-nitrophenyl)-1,2,3,4-tetrahydroquinolineHCID 21297656—
生成物1-(2-Aminophenyl)-6-methyl-1,2,3,4-tetra-hydroquinolineHCID 21299250—
生成物5-methyl-7-(4-methyl-1-piperazinyl)-2,3-dihydro-1H-quino[1,8-ab][1,5]-benzodiazepineHCID 21299254—

反応手順

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-tetra-hydroquinoline, N-[2-(6-methyl-1-phenyl)-1,2,3,4-tetrah quinolin-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.

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-d86be5753d494b37924d2fe3e7fba0ee
出典メモuspto-grants-1988_08