Derivatives of quinoline-8-carboxylic acid having pesticidal action

Abstract

Derivatives of quinoline-8-carboxylic acid having pesticidal action are disclosed, as are compositions comprising such derivatives.The quinoline-8-carboxylic acid derivatives which we have found to be effective pesticides include such derivatives having the general formula: ##STR1## in which R represents H, halogen, C.sub.1 -C.sub.3 alkyl, C.sub.2 -C.sub.6 alkenyl, CF.sub.3, C.sub.1 -C.sub.3 - alkoxyl or C.sub.1 -C.sub.3 - alkythio;X represents the group OY, in which Y is H, C.sub.1 -C.sub.6 alkyl, C.sub.2 -C.sub.6 alkenyl, C.sub.2 -C.sub.6 alkinyl optionally substituted, an alkali metal, an alkaline earth metal, a transition metal, Mn, NR.sub.2 in which both R equal or different have the same significance as above or are pyridines, aryl or alkyl or aralkylamines; and the quarternarized nitrogen salts of said compounds.The compounds having formula: I. are distinguished by having good activity as pesticides and, in particular, as insecticides.

Description

THE PRESENT INVENTION

The present invention concerns the use as pesticide agents of a class of compounds derived from quinoline-8-carboxylic acids, the compositions containing said compounds and the use of said compositions for the same purposes.

The compounds according to the invention belong to the class of the formula: ##STR2## in which R represents H, halogen, C.sub.1 -C.sub.3 alkyl, C.sub.2 -C.sub.6 alkenyl, CF.sub.3, C.sub.1 -C.sub.3 - alkoxyl or C.sub.1 -C.sub.3 - alkythio;

X represents the group OY, in which Y is H, C.sub.1 -C.sub.6 alkyl, C.sub.2 -C.sub.6 alkenyl, C.sub.2 -C.sub.6 alkinyl optionally substituted, an alkali metal, an alkaline earth metal, a transition metal, Mn, NR.sub.2 in which both R equal or different have the same significance as above or are pyridines, aryl or alkyl or aralkylamines; and the quarternarized nitrogen salts of said compounds.

Under the scope of this invention fall also the compositions containing as an active principle compounds according to this invention, such as wettable powders, emulsifiable oils, the granular and powdery formulates. The preparation of these compositions may be realized by operating according to the procedures known to the Prior Art.

The following examples are given to evidence the essential aspects of the invention, useful for an easy and precise understanding of the subject. However it must be understood that there may be introduced obvious variants to the technique of preparation of the compounds of the invention, variants, that is, in the use and in the method of application, without thereby deviating from the principle and protective scope of the invention.

EXAMPLE 1

Into a reactor fitted with a stirrer, a thermometer, a refluxer, a separating funnel and a heating bath, the following substances were introduced:

0.1 mole of anthranilic acid; 0.15 mole of glycerine; and a quantity of 85% sulphuric acid equal to the weight of the anthranilic acid. This mass was stirred and slowly heated up to a temperature of 100.degree. C., after which the heating was continued up to a temperature comprised between 140.degree. and 150.degree. C. at which the reaction started.

The reaction was lively and developed considerable heat. The mass was stirred for about 1 hour. Once the reaction was complete, 0.12 mole of metha-nitro-phenyl-sulphonic acid was added and the mass was refluxed for 4.5 hours. It was allowed to cool down and then poured into H.sub.2 O, from which the reaction product was extracted with methylene chloride. The extract was repeatedly washed with H.sub.2 O; the solvent was then evaporated at reduced pressure and the extract was left to crystallize at room temperature.

The residue obtained, when re-crystallized, had a melting point of 189.degree. C. and consisted of quinoline-8-carboxylic acid.

EXAMPLES 2 - 19

By operating as described in Example 1, but suitably varying the reactants, and/or carrying out successive reactions known in the art, the products reported in the following table were obtained.

TABLE__________________________________________________________________________ Physical-chemicalEx. Compound Characteristics and Bibliography__________________________________________________________________________ 2 ##STR3## melt. point 169.degree. C. (Chem. Zentralblatt 1934 I 1328-29) 3 ##STR4## decomposition at 220.degree. C. 4 ##STR5## -- 5 ##STR6## melt. point 185.degree. C. 6 ##STR7## melt. point >250.degree. C. 7 ##STR8## melt. point 171.degree.-173.degree. C. 8 ##STR9## -- 9 ##STR10## melting point 44.degree. C.10 ##STR11## melting point 190.degree. C.11 ##STR12## melting point 192.degree. C.12 ##STR13## melting point 155.degree. C.13 ##STR14## --14 ##STR15## --15 ##STR16## melting point 170-175.degree. C.16 ##STR17## melting point 120-130.degree. C.17 ##STR18## melting point 210.degree. C. dec.18 ##STR19## melting point 228-229.degree.C. (cfr. Lachowicz A. et al; Rocz. Chem. 1967 41(9) pp. 1543-59)19 ##STR20## --__________________________________________________________________________

EXAMPLE 20

Macrosiphum solani

Small potato plants, grown in pots, were contaminated with adult aphis females of the indicated species and, after a few hours, were sprayed with an aqueous dispersion of pesticides according to the invention. The percentages of mortality 24 hours after the treatment are shown in the following table.

______________________________________Compound Percentual mortality at a concentration of:No. 0.1% of active subst. 0.01% of active sub.______________________________________2 100 845 100 959 100 8810 100 8411 100 8513 100 68______________________________________

EXAMPLE 21

Aphis fabae

Small broad bean plants grown in pots were contaminated with young stage and adult aphides of the species indicated and, after a few hours, were sprayed with an aqueous dispersion of pesticides according to the invention. The mortality percentages 24 hours after the treatment are shown in the following Table.

______________________________________Compound Percentual mortality at a concentration of:No. 0.1% of active subst. 0.01% of active sub.______________________________________1 100 892 100 846 100 808 100 8819 100 82______________________________________

EXAMPLE 22

Leptinotarsa decemlineata

Small potato plants grown in pots and contaminated with 4-day old larvae of the indicated species were sprayed with an aqueous dispersion of a pesticide according to the invention. The following Table reports the mortality in percent of the larvae 48 hours after the treatment.

______________________________________ Percentual mortality at a concentration of:Compound 0.1% 0.05% 0.01%No. active sub active sub. active sub.______________________________________1 100 88 302 100 100 875 100 100 011 100 97 0______________________________________

EXAMPLE 23

Pieris brassicae

Cut cauliflower leaves were sprayed with an aqueous dispersion of pesticides according to the invention and, after drying, were contaminated with 5-day old larvae of the species indicated. The following Table reports the mortality in percent of the larvae 48 hours after the treatment.

______________________________________ Percentual mortality at a concentration of:Compound 0.1% 0.05% 0.01%No. active sub. active sub. active sub______________________________________1 85 23 02 100 100 833 100 100 55______________________________________

EXAMPLE 24

Spodoptera littoralis

Cut tobacco leaves were sprinkled with an aqueous dispersion of the compounds listed in the following Table, and after being dried were infected with 5-days old larvae of Spodotera littoralis.

______________________________________ Percentual mortality at a concentration of:Compound 0.1% 0.05% 0.01%No. active sub. active sub. active sub.______________________________________2 100 100 759 100 90 253 100 -- --______________________________________

Claims

1. A composition for combatting infestations due to Macrosiphum solani, Aphis fabae, Leptinotarsa decemlineata, Pieris brassicae, and Spodoptera littoralis, said composition consisting essentially of an aqueous dispersion of at least 0.05% by weight of an insecticide having the formula ##STR21## in which R is selected from the group consisting of H, halogen, and alkyl groups having from 1 to 3 carbon atoms; and

X represents NH.sub.2 or OY in which Y is selected from the group consisting of H, alkaline metals, alkaline earth metals; amines, and their quinoline salts with inorganic acids; and n-alkyl quinolinium salts.

2. The method of combatting infestations due to Macrosiphum solani, Aphis Labae, Leptinotarsa decemlineate, Pieris brassicae, and Spodoptera littoralis, which consists in applying to the habitat of said insects an aqueous dispersion of at least 0.05% of an insecticide having the formula ##STR22## in which R is selected from the group consisting of H, halogen, and alkyl groups having from 1 to 3 carbon atoms; and

X represents NH.sub.2 or OY in which Y is selected from the group consisting of H, alkaline metals, alkaline earth metals, amines, and their quinoline salts with inorganic acids and n-alkyl quinolinium salts.