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HRID 16544作成日:2026年10月25日

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

https://huagongshe.com/reaction/16544

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-chlorophenyl)ethanamineHCID 13110442—
生成物N-(Benzimidazol-2-yl)-2,2-bis(4-chlorophenyl)ethylamineHCID 11538181—

反応手順

The title compound was prepared from 2-chlorobenzimidazole and 2,2-bis(4-chlorophenyl)ethylamine (prepared by Procedure B from 2,2-bis(4-chloro-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 189-190° C.). MS(ES+) m/z 382 ([M+1]+, 100). 1NMR (DMSO-d6) δ 3.91 (m, 2H), 4.47 (t, 1H), 6.52 (m, 1H), 6.81-6.90 (m, 2H), 7.06-7.18 (m, 2H), 7.33-7.36 (m, 8H), 10.6 (s, 1 H).

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-cb90506abb62481699de42a7252ee56c
出典メモuspto-grants-2010_06