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HRID 34376作成日:2026年10月26日

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/reaction/34376

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-Fluoro-3-nitrotolueneHCID 136287—
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10-methyl-7-(4-methyl-1-piperazinyl)-2,3-dihydro-1H-quino[1,8-ab][1,5]benzodiazepineHCID 20129109—
生成物1-(4-Methyl-2-nitrophenyl)-1,2,3,4-tetrahydroquinolineHCID 21297653—
生成物2-[3,4-Dihydro-1(2H)-quinolinyl]-5-methylanilineHCID 21297677—

反応手順

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-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.

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-8740e8e630b54373bf00cc3743ff3746
出典メモuspto-grants-1988_08