If you mean the amine to be the nucleophile to react with the enone in a Michael reaction, the answer is: No, because the active methylene is going to react instead. Since Michael additions go under thermodynamic conditions, you have a problem to control the regioselectivity in this case. I think you should reconsider your synthesis strategy.

Read more on the possibilities here:

http://www.metallacycle.com/chemistry/organic/asymmetric-synthesis/pdfs/13%20Michael%20Reaction.pdf

You should show the reaction and it will be easier toprovide amore precise answer

Thank you very much Monsurat Lawal.

Try LiClO4 mediated Michel addition.