反応 #166020

ord-b5d33fa1f90b463887abfcf524328a3e

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他LC/MS [10.01 min; 480 (M+1)]

実験手順

N-Benzyloxy-3-(2-chloro-4-iodo-phenylamino)-isonicotinamide was synthesized according to the procedure for General Method 1, outlined above, starting with 0.25 mmol of 3-[(2-chloro-4-iodophenyl)amino]isonicotinic acid (intermediate 2) and 0.36 mmol of O-methyl-hydroxylamine. LC/MS [10.01 min; 480 (M+1)]

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08841459B2uspto-grants-2014_09