Propane trimethylamine

Betanechol Betanechol, 2-carbamoyloxy-l-(A,A,iV-trimethyl)propyl ammonium chloride (13.1.8), is made by either the subsequent reaction of l-(iV,A,A-trimethylammonium) propan-2-ol with phosgene, followed by ammonia, or by a completely analogous synthesis of carbachol by the reaction of l-chloro-2-propanol with phosgene followed by consequent reactions with ammonia, and then with trimethylamine, giving betanechol (13.1.8) [14,15],... 

In the names of amines, the general use of suffixes and prefixes is not always observed. Normally, the suffix -amine would be added to the name of the parent hydride and engender names such as methanamine (CH3-NH2). Further substitution on the nitrogen atom would then be indicated by prefixes, leading to names that appear very cumbersome, such as A -methylmethanamine for (CH3)2NH and N,N-dimethylmethanamine for (CH3)3N. The traditional names of methylamine, di-methylamine and trimethylamine are much simpler. In these names, the term amine is not a suffix. It is, in fact, the name of the parent hydride, NH3, which now serves as the basis of substitutive names. Names such as diethylamine and tributylamine are representative of the preferred nomenclature. Diamines are named accordingly, as with ethane-1,2-diamine for H2N-CH2-CH2-NH2 and propane-1,3-diamine for H2N-[CH2]3-NH2. There are allowed alternatives for these last two compounds ethylenediamine and propane-1,3-diyldiamine. 

Ans. Compound I ethylamine or ethanamine. Compound II trimethylamine or Af,Ai-Dimethyl-aminomethane. Compound III methylpropylamine or l-(N-methylamino)propane. Compound IV i-butylethylmethylamine or 2-(iV-ethyl-Af-methylamino)butane. (Parentheses are used in the second names for compounds III and IV to avoid ambiguity.)... 

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