Can someone help me with this, The major product in the following reaction is:

Basicity of Aromatic Amines -

The unshared pair of electrons at the nitrogen atom is in resonance with the benzene ring and hence not fully available for donation as in the case of aniline.

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Nature of group and basicity -

Electron withdrawing groups ( -I and -M  effect ) decreases basicity, whereas Electron releasing groups ( +I and +M  effect ) increases basicity.

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 1,3,7 Nitrogen have localised lone pair

  They have delocalised lone pair so, they are less nucleophilic and less basic

1&3 Nitrogen is mare Nucleophilic and more basic as compared to Nitrogen

 Moreover, 3-Nitrogen is most Nucleophilic because of less crowding

                                    More  because of less crowding

                                                                                density more at 1,3

                                                                                 But 3rd N is most