Ammonia, because of nitrogen's lone pair, is a nucleophilic species. Methyl chloride has an electrophilic carbon. The two will react in a substitution reaction to produce CH3NH2. Since a byproduct of the reaction is HCl, this can be protonated to form CH3NH3+. However, since methyl groups are electron-donating, methylating the nitrogen will only increase its nucleophilicity, so the resulting primary amine will react with additional methyl chloride molecules to form the secondary amine, then the tertiary amine, and finally, the quatenary amine, N(CH3)4+. Therefore, the primary salt will be N(CH3)4Cl, with minor amounts of the primary, seconday, and tertiary ammonium chlorides.