Twenty-seven carboxamide derivatives of
(±)-cis-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropanecarboxylic acid (permethrin acid) have been synthesized and evaluated
in the laboratory against
mosquito larvae (Aedes aegypti). These
cis-cyclopropylcarboxamides, with
N-(substituted)phenyl,
N-(substituted)phenylmethyl,
N-(substituted)phenylethyl, N-phenylpropyl,
and N-phenylbutyl
groups, were synthesized from the acid chloride of permethrin acid and
various arylamines in
methylene chloride. The samples were characterized by
13C NMR spectroscopy and mass
spectrometry. Secondary amides with electron-donating (e.g.,
methoxy) and electron-withdrawing
(e.g., trifluoromethyl) substituents on the phenyl ring as well as nine
tertiary amides were
investigated.
3-(2,2-Dichloroethenyl)-2,2-dimethyl-N-(3-phenoxyphenyl)methylcyclopropanecarboxamide
was the most active experimental compound and was 25 times less potent
than (±)-cis-permethrin.
Cyclopropylcarboxamides of the
N-(substituted)phenyl,
N-(substituted)phenylethyl, and
N-phenylpropyl types were essentially inactive in the larvicidal
tests.
Keywords: Pyrethroid amides; synthesis; purification; spectroscopy;
mosquitoes; larvicidal activity
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