반응 #44836

ord-2b886003c897496299a5a3d19c74f014

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The product was purified by recrystallisation

실험 절차

The title compound was prepared from 2-chlorobenzimidazole and 5 ,7-dimethyl-1,2,3,4-tetrahydro-1-naphthylamine (prepared by Procedure B from 5,7-dimethyl-1-tetralone) by Procedure A (60 min at 170° C. followed by 20 min at 200° C.). The product was purified by recrystallisation to give the title compound as the free base and as a mixture of enantiomers (white solid, mp 250-252° C.). MS(ES+) m/z 292 ([M+1]+, 100).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07737167B2uspto-grants-2010_06