HRID1958184

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID24229645

4-Methyl-3,4-dihydro-2H-pyrido[3,2-b][1,4]oxazine-7-carboxylic acid

C9H10N2O3

HCID67281315

5-(4-Chlorophenyl)-6-(2,2,2-trifluoroethoxy)-3-pyridinamine

C13H10ClF3N2O

PRODUCTS

生成物

结构：CN1CCOc2cc(C(=O)Nc3cnc(OCC(F)(F)F)c(-c4ccc(Cl)cc4)c3)cnc21

HCID56961947

未命名化合物

PROCEDURE

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 3,4-dihydro-4-methyl-2H-pyrido[3,2-b]-1,4-oxazine-7-carboxylic acid (CAN 915707-58-3) as starting materials; MS (EI) 479.2 (M+H)+.