NH protons not appearing in H NMR spectrum of 3,4-dihydropyrimidone ...

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If you have integrated that peak, you'd see the integration value is more than 3-protons of the real compound. That means your compound is really wet when you take the NMR. The following diagram shows ratios of water peak to TMS and residual $\ce{CHCl3}$ peaks in a typical $\ce{CDCl3}$ (with 99.8% $\ce{D}$ and 0.05% TMS) solvent bottle (Ref.1):


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