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HRID 585392作成日:2026年10月26日

4-(3-(Trifluoromethyl)Phenyl)Piperidine → 9-[1-(3,4-Dimethoxybenzoyl)-2-[5-[4-[3-(trifluoromethyl)phenyl]-1-piperidinyl]pentyl]-1,2,3,4-tetrahydro-4-quinolinyl]-9H-carbazole

https://huagongshe.com/reaction/585392

反応式

関与物質

役割名称HCID仕込み量
反応物4-(3-(Trifluoromethyl)Phenyl)PiperidineHCID 11736340—
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-[3-(trifluoromethyl)phenyl]-1-piperidinyl]pentyl]-1,2,3,4-tetrahydro-4-quinolinyl]-9H-carbazoleHCID 2233934753.5%

反応手順

Starting with 5-[4-(9H-9-carbazolyl)-1-(3,4-dimethoxybenzoyl)-1,2,3,4-tetrahydro-2-quinolinyl]-1-pentanol (0.19 g, 0.32 mmol) prepared in Example 135 and 4-[3-(trifluoromethyl)phenyl]piperidine (0.23 g, 1 mmol), the same procedure as shown in Example 136 was repeated to give the titled compound (0.13 g, yield: 53%) as a white crystal (cis:trans=3:1).

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-eb711abbb77f45098a00c173954b7cb2
出典メモuspto-grants-2005_08