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HRID 4029作成日:2026年10月23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/ja/reaction/4029

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N-[2-(2,3-dihydro-1H-indol-1-yl)-5-fluorophenyl]-4-methyl-1-piperazine carboxamide maleateHCID 70406853—
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-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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04723007
出典データセットuspto-grants-1988_02
ORD IDord-50db5f899137486aaab10e21f98eedfe
出典メモuspto-grants-1988_02