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HRID 585391作成日:2026年10月27日

1-(4-Fluorophenyl)piperazine → 9-[1-(3,4-Dimethoxybenzoyl)-2-[5-[4-(4-fluorophenyl)-1-piperazinyl]pentyl]-1,2,3,4-tetrahydro-4-quinolinyl]-9H-carbazole

https://huagongshe.com/reaction/585391

反応式

関与物質

役割名称HCID仕込み量
反応物1-(4-Fluorophenyl)piperazineHCID 75260—
反応物5-[4-(9H-9-Carbazolyl)-1-(3,4-dimethoxybenzoyl)-1,2,3,4-tetrahydro-2-quinolinyl]-1-pentanolHCID 22339233—
生成物9-[1-(3,4-Dimethoxybenzoyl)-2-[5-[4-(4-fluorophenyl)-1-piperazinyl]pentyl]-1,2,3,4-tetrahydro-4-quinolinyl]-9H-carbazoleHCID 2233923751.2%

反応手順

Starting with 5-[4-(9H-9-carbazolyl)-1-(3,4-dimethoxybenzoyl)-1,2,3,4-tetrahydro-2-quinolinyl]-1-pentanol (0.13 g, 0.22 mmol) prepared in Example 135 and 4-(4-fluorophenyl)piperazine (79 mg, 0.44 mmol), the same procedure as shown in Example 136 was repeated to give the titled compound (0.08 g, yield: 51%) as a white crystal (cis:trans=4:1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06930104B2
出典データセットuspto-grants-2005_08
ORD IDord-e62ec86fe7db49bc97eab548353d5ccf
出典メモuspto-grants-2005_08