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HRID 16543作成日:2026年10月26日

2-Chlorobenzimidazole → N-(Benzimidazol-2-yl)-2,2-bis(4-fluorophenyl)ethylamine

https://huagongshe.com/reaction/16543

反応式

関与物質

役割名称HCID仕込み量
反応物2-ChlorobenzimidazoleHCID 78572—
反応物2,2-Bis(4-fluorophenyl)ethanamineHCID 819761—
生成物N-(Benzimidazol-2-yl)-2,2-bis(4-fluorophenyl)ethylamineHCID 11552019—

反応手順

The title compound was prepared from 2-chlorobenzimidazole and 2,2-bis(4-fluorophenyl)ethylamine (prepared by Procedure B from 2,2-bis(4-fluoro-phenyl)acetaldehyde) by Procedure A (20 min at 170° C.). The product was isolated by preparative LCMS to give the title compound as the free base (white solid, mp 155-157° C.). MS(ES+) m/z 350 ([M+1]+, 100) 1NMR (DMSO-d6) δ 3.90 (m, 2H), 4.46 (t, 1H), 6.50 (m, 1H), 6.80-6.90 (m, 2H), 7.07-7.18 (m, 6H), 7.35-7.42 (m, 4H), 10.5 (s, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737167B2
出典データセットuspto-grants-2010_06
ORD IDord-d4650308ee104cf59a72eb3ca6abb17b
出典メモuspto-grants-2010_06