HRID1958191
反应详情
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实验过程
The title compound was synthesized in analogy to Example 42 g, using 5-(4-chloro-phenyl)-6-(2 ,2,2-trifluoro-ethoxy)-pyridin-3-ylamine (example E) and 5-methoxy-3-pyridinecarboxylic acid (CAN 20826-03-3) as starting materials; LC-MS (UV peak area/ESI) 97.8%, 438.0812 (M+H)+.