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3 Brief Demonstration of the General Nomenclature Rules
Ph
/
Ph-CO-N
N-Methylbenzanilide
\
(N-Methyl-N- phenylbenzamide)
Me
Amides whose nitrogen atom is part of a ring are generally regarded as
acylated heterocycles, subordinate groups gaining preference only when
attached to the same ring.
o
7"-N)--OH
Me
1-Acetylazetidin-3-01
but:
2-( 4-Hydroxybenzoyl)-2H-indole
For lactams and similar compounds in most cases the conventional trivial
names of Table 8 are applied although here too heterocyclic nomenclature
would render much more uniform names possible.
o
Me X; NH 3,4-Dim,thylpynolidio-2-00'
Me
Imines form the functional compound class of lowest rank and are
hence named as such only when no N-organyl substituents are present;
otherwise they are named as ... ylidenamines. If more senior functions are to be respected ... imino prefixes are used. Totally systematic
azane-based names would again bring about considerable simplifications.
NH
'/
Ph-C
\
H
subst.: Phenylmethanimine
conj.: Benzenemethanimine
new: (Phenylmethylen)azane
NPh
//
Ph-C
\
H
syst.: N-(Phenylmethylene) benzenamine
trad.: Benzyliden- or Benzalaniline
new: Phenyl(phenylmethylen)azane
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