Reaktion #165529

ord-d83345b9e3ed4c89a71eb51d0f208525

Reaktionsgleichung

Cc1ccc(N)cc1O
5-amino-2-methylphenol
CNC(=O)c1cc(Cl)ccn1
4-chloro-N-methyl-2-pyridinecarboxamide
CNC(=O)c1cc(Oc2cc(N)ccc2C)ccn1
3-(2-(N-methylcarbamoyl)-4-pyridyloxy)-4-methylaniline

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigehad been synthesized

Vorschrift

Entry 18: 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. 5-(Trifluoromethyl)-2-methoxyaniline was converted into 5-(trifluoromethyl)-2-methoxyphenyl isocyanate according to Method B1. 5-(Trifluoromethyl)-2-methoxyphenyl isocyanate was reacted with 3-(2-(N-methylcarbamoyl)-4-pyridyloxy)-4-methylaniline according to Method C1a to afford the urea.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08841330B2uspto-grants-2014_09