反応 #66895

ord-b856ce1bf2d94008be30285146c297cd

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他to yield 56 mg (40%)

実験手順

The title compound was synthesized in analogy to Example 89 from N-(3,4-dichlorophenyl)-5,6,7,8-tetrahydropyrido[3′,4′:4,5]thieno[2,3-d]pyrimidin-4-amine from Example 76A (100 mg, 0.29 mmol) and (2E)-4-[methyl(1-methylethyl)amino]but-2-enoic acid hydrochloride from Example 2A (77 mg, 0.40 mmol) to yield 56 mg (40%).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08524722B2uspto-grants-2013_09