反应 #163608

ord-e70c683f8db84e40be1c3cfb70caaa9d

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他were reacted

实验过程

In a like manner to the preparation of 2-chloro-N4-(3,4-ethylenedioxyphenyl)-5-fluoro-4-pyrimidineamine, 2,4-dichloro-5-fluoropyrimidine and ethyl 1-(3-aminobenzyl)piperidine-4-carboxylate were reacted to provide 2-chloro-N4-[3-[[4-(ethoxycarbonyl)piperidino]methyl]phenyl]-5-fluoro-4-pyrimidineamine. LCMS: purity: 97%; MS (m/e): 394 (MH+).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08835430B2uspto-grants-2014_09