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HRID 710445作成日:2026年10月26日

5-((2'-(Trifluoromethyl)biphenyl-4-yl)ethynyl)-1H-indole → 5-(2-(2'-(Trifluoromethyl)biphenyl-4-yl)ethyl)-1H-indole

https://huagongshe.com/reaction/710445

反応式

関与物質

役割名称HCID仕込み量
反応物5-((2'-(Trifluoromethyl)biphenyl-4-yl)ethynyl)-1H-indoleHCID 66726787—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
生成物5-(2-(2'-(Trifluoromethyl)biphenyl-4-yl)ethyl)-1H-indoleHCID 6672661598%

反応手順

A suspension of the product of Step B (0.25 g, 0.7 mmol) and 10% Pd/C (0.1 g) in EtOH (10 ml) was stirred overnight under H2. The mixture was filtered through Celite bead and the filtrate was evaporated to dryness to give the desired product (0.25 g, 98%) as pale paste. 1H-NMR (CDCl3) 2.97-3.1 (m, 4H); 6.5 (m, 1H); 7.04 (dd, 1H, J=1.37, 8.3 Hz), 7.15-7.2 (m, 2H); 7.30-7.34 (m, 2H); 7.37-7.44 (m, 2H); 7.51 (d, 1H, J=7.56 Hz); 8.68 (broad s, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09181182B2
出典データセットuspto-grants-2015_11
ORD IDord-168060126ce04fa8bc8df16de9f7b969
出典メモuspto-grants-2015_11