i dunno an mnemonic, but to remember imine/enamine, just think of it as analogous to keto/enol of a carbonyl.
An imine is a like the keto form, except the oxygen is replaced by a nitrogen.
An enamine is like the enol form, except the oxygen is replaced by a nitrogen.
(In fact, imine and enamine tautomerize just like keto/enol)
Amide, just think of amino acid peptide bonds.
Amines are just like ammonia with stuff (hydrogens) replaced by carbons.