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Structures of acetamidine and imidazoline

My approach:

  1. Conjugate acids of both molecules have the same number of stable resonance structures. So no conclusion from here.
  2. Conjugate acid of 2-imidazoline will have negative inductive on the lone pair donating nitrogen by the other nitrogen atom. Since this effect is absent in acetamidine, acetamidine should be a stronger base.

Is the above approach right? Can ring strain affect the basic strength of 2-imidazoline in any way? Should I consider any other factor too to make the right comparison of the basic strength of the above two molecules?

Related Questions:

Comparing basicity of imidazole and 2-imidazoline

How to predict the basicity of organic amines?

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