反応 #165560

ord-73a48bacdb214a53a62c5846c0c0a299

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他had been synthesized

実験手順

Entry 90: According to Method A2, Step 4, 5-amino-2-methylphenol was reacted with 4-chloro-N-methyl-2-pyridinecarboxamide, which had been synthesized according to Method A2, Step 3b, to give 3-(2-(N-methylcarbamoyl)-4-pyridyloxy)-4-methylaniline. 4-Bromo-3-(trifluoromethyl)aniline was converted into 4-bromo-3-(trifluoromethyl)phenyl isocyanate according to Method B1. According to Method C1a, 4-bromo-3-(trifluoromethyl)phenyl isocyanate was reacted with 3-(2-(N-methylcarbamoyl)-4-pyridyloxy)-4-methylaniline to afford the urea.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08841330B2uspto-grants-2014_09