3-(丙烷-2-基)苯基]甲胺

反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: The title compound was prepared following the same general protocol as described in Step 8-9, Example 1, using the (3-isopropylphenyl)methanamine and the 1-((2′-(tert-butoxycarbonyl)-[1,1′-biphenyl]-4-yl)methyl)-2,3-dimethyl-1H-indole-5-carboxylic acid. ESI-MS (m/z): 531 [M+H]+.

反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: The following compounds can be obtained by a similar procedure, using 3-methoxy-benzylamine, 2-pyridin-4-yl-ethylamine, 2-(3,4-dimethoxy-phenyl)-ethylamine or 3-isopropyl-benzylamine instead of 3-methyl-benzylamine: The following compounds can be obtained by a similar procedure