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HRID 392297作成日:2026年10月24日

1-(Bromomethyl)-2-(trifluoromethyl)benzene → {[6-(3-Pentyl-1-[2-(trifluoromethyl)benzyl]-1H-indol-2-yl)-2-naphthyl]oxy}acetonitrile

https://huagongshe.com/ja/reaction/392297

反応式

関与物質

役割名称HCID仕込み量
反応物1-(Bromomethyl)-2-(trifluoromethyl)benzeneHCID 123057—
反応物{[6-(3-pentyl-1H-indol-2-yl)-2-naphthyl]oxy}acetonitrileHCID 11337627—
生成物{[6-(3-Pentyl-1-[2-(trifluoromethyl)benzyl]-1H-indol-2-yl)-2-naphthyl]oxy}acetonitrileHCID 11364499—

反応手順

The title compound was prepared as a solid (0.147 g, 34%) from {[6-(3-pentyl-1H-indol-2-yl)-2-naphthyl]oxy}acetonitrile using 2-trifluoromethyl benzyl bromide and the procedure from step 4 of Example 2; 1H NMR (DMSO-d6) δ 0.72 (t, J=7.8 Hz, 3H), 1.08-1.29 (m, 4H), 1.51-1.67 (m, 2H), 2.71 (t, J=8.6 Hz, 2H), 5.29 (s, 2H), 5.47 (s, 2H), 6.37 (d, J=8.6 Hz, 1H), 7.08-7.21 (m, 2H), 7.23-7.32 (m, 2H), 7.35-7.45 (m, 2H), 7.48 (t, J=7.8 Hz, 1H), 7.53 (d, J=1.7 Hz, 1H), 7.63-7.75 (m, 2H), 7.83-7.92 (m, 3H); mass spectrum [(+) ESI], m/z 527 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06800654B2
出典データセットuspto-grants-2004_10
ORD IDord-6ee3d1d87d7c44b2b1b33ea973fbc78b
出典メモuspto-grants-2004_10