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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 16543생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/16543

반응식

참여 물질

역할이름HCID투입량
반응물2-ChlorobenzimidazoleHCID 78572—
반응물2,2-Bis(4-fluorophenyl)ethanamineHCID 819761—
생성물N-(Benzimidazol-2-yl)-2,2-bis(4-fluorophenyl)ethylamineHCID 11552019—

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737167B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-d4650308ee104cf59a72eb3ca6abb17b
출처 메모uspto-grants-2010_06