反应 #44071

ord-b8afcca6807f4627ac2c4ceac63bd526

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

The title compound was prepared in 30% yield according to the general procedure for the preparation of the amides (Method B) starting from 3-{2-[4-(2-methyl-5-quinolinyl)-1-piperazinyl]ethyl}aniline (D6) and cyclohexanecarbonyl chloride.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07732600B2uspto-grants-2010_06