Quinoline-3-carboxamides, their manufacture and use

Abstract

Quinoline-3-carboxamides I ##STR1## where R.sup.1 is hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, and the organic radicals may be substituted or unsubstituted;R.sup.2 is hydrogen, hydroxyl, alkoxy, alkenyloxy, dialkylamino, alkyl, alkenyl, alkynyl, cycloalkyl, and the organic radicals may be substituted or unsubstituted;orR.sup.1, R.sup.2 together denote an alkylene chain of 4 to 7 members and which may be interrupted by oxygen, sulfur or N-methyl;R.sup.3 -R.sup.6 are hydrogen, alkyl, alkoxy, haloalkyl, haloalkoxy, alkylthio, haloalkylthio, halogen, cyano or nitro;X is oxygen or sulfur;with the proviso that R.sup.2 is not hydrogen, C.sub.1 -C.sub.3 -alkyl, n-butyl, 3-methylbutyl, cyclohexyl, hexyl, heptyl, octyl, 2-chlorobenzyl, 3-(dimethylamino)propyl, 3-(diethylamino)propyl, 2-morpholinoethyl or 2-(3,4-dimethoxyphenyl)ethyl when R.sup.1 and R.sup.3 to R.sup.6 are hydrogen and X is oxygen, and that R.sup.2 is not benzyl when R.sup.1 is methyl, R.sup.3 to R.sup.6 are hydrogen and X is oxygen, and that R.sup.1 and R.sup.2 do not jointly denote morpholino when R.sup.3 to R.sup.6 are hydrogen and X is oxygen.

Description

The present invention relates to quinoline-3-carboxamides of the formula I ##STR2## where the substituents have the following meanings: R.sup.1 hydrogen, C.sub.1 -C.sub.25 -alkyl, C.sub.3 -C.sub.25 -alkenyl, C.sub.3 -C.sub.25 -alkynyl or C.sub.3 -C.sub.8 -cycloalkyl, where these groups may carry from one to five halogen atoms and/or from one to three of the following radicals: cyano, C.sub.3 -C.sub.8 -cycloalkyl, C.sub.1 -C.sub.4 -alkoxy, C.sub.1 -C.sub.4 -haloalkoxy, C.sub.1 -C.sub.4 -alkylthio, C.sub.1 -C.sub.4 -haloalkylthio, di-C.sub.1 -C.sub.4 -alkylamino, phenyl, phenylthio, phenoxy, and the phenyl radicals in turn may bear from one to three of the following groups: C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -alkoxy, C.sub.1 -C.sub.4 -haloalkyl, C.sub.1 -C.sub.4 -haloalkoxy, halogen, cyano or nitro;

R.sup.2 hydrogen, hydroxyl, C.sub.1 -C.sub.8 -alkoxy, C.sub.3 -C.sub.8 -alkenyloxy, di-C.sub.1 -C.sub.4 -alkylamino, C.sub.1 -C.sub.25 -alkyl, C.sub.3 -C.sub.25 -alkenyl, C.sub.3 -C.sub.25 -alkynyl or C.sub.3 -C.sub.8 -cycloalkyl, where these groups may carry from one to five halogen atoms and/or from one to three of the following radicals: cyano, C.sub.3 -C.sub.8 -cycloalkyl, C.sub.1 -C.sub.4 -alkoxy, C.sub.1 -C.sub.4 -haloalkoxy, C.sub.1 -C.sub.4 -alkylthio, C.sub.1 -C.sub.4 -haloalkylthio, di-C.sub.1 -C.sub.4 -alkylamino, phenyl, phenylthio, phenoxy, and the phenyl radicals in turn may bear from one to three of the following groups: C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -alkoxy, C.sub.1 -C.sub.4 -haloalkyl, C.sub.1 -C.sub.4 -haloalkoxy, halogen, cyano or nitro; R.sup.2 further denotes substituted C.sub.1 -C.sub.8 -alkoxy, C.sub.3 -C.sub.8 -alkenyloxy, di-C.sub.1 -C.sub.4 -alkylamino, C.sub.1 -C.sub.25 -alkyl, C.sub.1 -C.sub.25 -alkenyl, C.sub.3 -C.sub.25 -alkynyl or C.sub.3 -C.sub.8 -cycloalkyl, where these groups are substituted by from one to five halogen atoms and/or by one or two 5- to 6-membered heterocyclic, aliphatic or aromatic radicals containing from one to three heteroatoms selected from the group consisting of oxygen, sulfur and nitrogen, and which radicals may bear one or two of the following substituents: halogen, C.sub.1 -C.sub.3 -alkyl or C.sub.1 -C.sub.3 -alkoxy; or R.sup.1, R.sup.2 together denote an alkylene chain of 4 to 7 members and which may be interrupted by oxygen, sulfur or N-methyl; R.sup.3 -R.sup.6 hydrogen, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -alkoxy, C.sub.1 -C.sub.4 -haloalkyl, C.sub.1 -C.sub.4 -haloalkoxy, C.sub.1 -C.sub.4 -alkylthio, C.sub.1 -C.sub.4 -haloalkylthio, halogen, cyano or nitro; X oxygen or sulfur or environmentally tolerated salts thereof; with the proviso that R.sup.2 is not hydrogen, C.sub.1 -C.sub.3 -alkyl, n-butyl, 3-methylbutyl, cyclohexyl, hexyl, heptyl, octyl, 2-chlorobenzyl, 3-(dimethylamino)propyl, 3-(diethylamino)propyl, 2-morpholinoethyl or 2-(3,4-dimethoxyphenyl)ethyl when R.sup.1 and R.sup.3 to R.sup.6 are hydrogen and X is oxygen, and with the proviso that R.sup.2 is not benzyl when R.sup.1 is methyl, R.sup.3 to R.sup.6 are hydrogen and X is oxygen, and further with the proviso that R.sup.1 and R.sup.2 do not together denote morpholino when R.sup.3 to R.sup.6 are hydrogen and X is oxygen.

The invention further relates to herbicidal agents containing compounds I as active ingredients, and the herbicidal use of quinoline-3-carboxamides of the formula I, including the compounds disclaimed in the disclaimer.

The compounds of the formula I may be present in the following tautomeric forms, which are also encompassed by the invention: ##STR3##

4-Hydroxycarbostyryls having anti-inflammatory and anti-allergic properties are known from Chemical Abstracts, Vol. 113, No. 211864z.

Quinoline-3-carboxamides having anticoagulant (Khim.-Farm. Zh., 24(4), 31 (Russ), 1990) and antibacterial (Chemical Abstracts 70, Nr. 67681x) properties, and derivatives acting as local anesthetics (Farm. zh. (Kiev) (2), 78,1991), are also known.

The object of the present invention was to provide novel, herbicidally effective quinoline-3-carboxamides and methods of preparing them.

This object was achieved by the quinoline-3-carboxamides I, methods of preparing them and herbicidal agents containing the compounds I. Salts of the compounds I are also encompassed by the invention.

The quinoline-3-carboxamides I are obtained for example by reacting a quinoline-3-carboxylate of the formula IIa in conventional manner (Khim.-Farm. Zh., Vol. 24, issue 4, pp. 31 and 32 (Russ.) = pp. 257-259 (Engl.), 1990), in the presence or absence of an organic solvent, with a substituted amine of the formula III: ##STR4##

R.sup.7 in formula IIa is a low-molecular-weight alkyl group, preferably C.sub.1 -C.sub.4 -alkyl such as methyl, ethyl, propyl, 1-methylethyl, butyl, 1-methylpropyl, 2-methylpropyl or 1,1-dimethylethyl.

The reaction is generally carried out at from 20.degree. C. to 250.degree. C., preferably 100.degree. C. to 180.degree. C., in an inert organic solvent.

Examples of suitable solvents or diluents are aliphatic, alicyclic and aromatic hydrocarbons, such as pentane, hexane, cyclohexane, benzene, toluene, and xylenes; ethers such as diethyl and di-n-butyl ether, methyl tert.-butyl ether, dimethoxyethane, ethylene glycol dimethyl ether, tetrahydrofuran and dioxane; alcohols such as methanol, ethanol, propanol and butanol; and aprotic dipolar solvents such as dimethylformamide, dimethyl sulfoxide and pyridine.

Mixtures of these substances may also be used as solvents and diluents.

The starting materials are generally reacted with each other in stoichiometric amounts. It may be advantageous, for instance to increase the yield, to use one of the starting materials, preferably the amine, in an excess of 0.1 to 10 mole equivalents.

The reaction is generally carried out at atmospheric pressure. However, it may be advantageous, depending on the type of amine employed, to carry out the reaction at superatmospheric pressure, especially autogenously increased pressure, in an autoclave.

The compounds I may also be obtained from quinoline-3-carboxylic acids IIb by first converting IIb in conventional manner into the halide or another active form of the carboxylic acid function, and then amidating this derivative with an amine III. ##STR5##

Examples of active forms of the carboxylic acids are, in addition to the halides (especially chlorides and bromides), imidazolides. Generally, the halides are preferred.

They are obtained by reacting the carboxylic acids IIb with a halogenating agent such as phosgene, thionyl chloride, phosphorus oxychloride, and phosphorus tri- and -pentachloride.

The subsequent amidation is carried out at from (-20.degree.) to 80.degree. C., preferably from 0.degree. to 30.degree. C., in an inert organic solvent.

Suitable solvents for this reaction are, in particular, hydrocarbons such as benzene and toluene, halohydrocarbons such as dichloromethane, and ethers such as diethyl ether and tert-butyl methyl ether.

As hydrogen halide is formed on the amidation of acid halides, it is advantageous for increasing the yield to use the amine III in an excess, or to add an acid-binding agent such as triethylamine.

The quinoline-3-carboxamides I may advantageously be prepared from the carboxylic acids IIb in a single stage: the carboxylic acid IIb is reacted with an amine III in conventional manner (WO 90 15052) in the presence of a dehydrating agent, e.g., propanephosphonic anhydride or dicyclohexylcarbodiimide, at from 0.degree. to 50.degree. C., preferably 5.degree. to 25.degree. C., in an inert solvent such as dichloromethane, tetrahydrofuran, toluene or ethyl acetate.

Compounds of the formula I in which X is oxygen and R.sup.1 is hydrogen may also be obtained in conventional manner (J. Org. Chem. Vol. 44, pp. 4877 et seq. (1979)) by reacting a 2,4-dihydroxyquinoline IV with an isocyanate of the formula V. ##STR6##

The quinoline-3-carboxylic acids and esters of the formula II are known or may be prepared by known methods (Australian J. Chem. Vol. 7, p. 348, p. 368 (1954)).

The 2,4-dihydroxyquinolines IV are also known or may be prepared by known methods, e.g., Monatsh. Chem., Vol. 96, 418 (1965).

The amines of the formula III and isocyanates of the formula V required for the reactions are either known or commercially available, or may be prepared by generally known chemical processes.

In view of the use to which the quinoline-3-carboxamides of the formula I are to be put, the following radicals are suitable substituents:

R.sup.1

hydrogen, branched or straight-chain C.sub.1 -C.sub.25 -alkyl, such as methyl, ethyl, propyl, 1-methylethyl, butyl, 1-methylpropyl, 2-methylpropyl, 1,1-dimethylethyl, pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, 2,2-dimethylpropyl, 1-ethylpropyl, hexyl, 1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1,1-dimethylbutyl, 1,2-dimethylbutyl, 1,3-dimethylbutyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl, 1-ethylbutyl, 1,1,2-trimethylpropyl, 1,2,2-trimethylpropyl, 1-ethyl-1-methylpropyl, 1-ethyl-2-methyl-propyl, heptyl, 1-methylheptyl, octyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, nonadecyl, arachidyl, heneicosanyl, docosyl, tricosyl, tetracosyl and pentacosyl; especially C.sub.1 -C.sub.15 -alkyl, for example C.sub.1 -C.sub.6 -alkyl, such as methyl, ethyl, 1-methylethyl, 1-methylpropyl, 2-methylpropyl, 1,1-dimethylethyl and 1,1-dimethylpropyl; branched or straight-chain C.sub.3 -C.sub.25 -alkenyl, such as 2-propenyl, 2-butenyl, 3-butenyl, 1-methyl-2-propenyl, 2-methyl-2-propenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, 3-methyl-2-butenyl, 1-methyl-2-butenyl, 2-methyl-2-butenyl, 1-methyl-3-butenyl, 2-methyl-4-butenyl, 3-methyl-3-butenyl, 1,1-dimethyl-2-propenyl, 1,2-dimethyl-2-propenyl, 1-ethyl-2-propenyl, 2-hexenyl, 3-hexenyl, 4-hexenyl, 5-hexenyl, 1-methyl-2-pentenyl, 2-methyl-2-pentenyl, 3-methyl-2-pentenyl, 4-methyl-2-pentenyl, 1-methyl-3-pentenyl, 2-methyl-3-pentenyl, 3-methyl-3-pentenyl, 4-methyl-3-pentenyl, 1-methyl-4-pentenyl, 2-methyl-4-pentenyl, 3-methyl-4-pentenyl, 4-methyl-4-pentenyl, 1,1-dimethyl-2-butenyl, 1,1-dimethyl-3-butenyl, 1,2-dimethyl-2-butenyl, 1,2-dimethyl-3-butenyl, 1,3-dimethyl-2-butenyl, 1,3-dimethyl-3-butenyl, 2,2-dimethyl-3-butenyl, 2,3-dimethyl-2-butenyl, 2,3-dimethyl-3-butenyl, 1-ethyl-2-butenyl, 1-ethyl-3-butenyl, 2-ethyl-2-butenyl, 2-ethyl-3-butenyl, 1,1,2-trimethyl-2-propenyl, 1-ethyl-1-methyl-2-propenyl and ethyl-2-methyl-2-propenyl, 10-undecenyl, 9-tetradecenyl, 9-hexadecenyl, 6-octadecenyl, 9-octadecenyl, 11-octadecenyl, 9,12-octadecadienyl, 11-eicosenyl, 13-eicosenyl and 13-docosenyl; especially C.sub.3 -C.sub.15 -alkenyl, for example C.sub.3 -C.sub.6 -alkenyl, such as 2-propenyl, 2-butenyl, 3-butenyl, 1-methyl-2-propenyl, 2-methyl-2-propenyl and 1-methyl-2-butenyl; C.sub.3 -C.sub.25 -alkynyl, especially C.sub.3 -C.sub.15 -alkynyl, particularly preferably C.sub.3 -C.sub.8 -alkynyl, e.g., propargyl, 2-butynyl, 3-butynyl, 2-pentynyl, 3-pentynyl, 4-pentynyl, 1-methyl-3-butynyl, 2-methyl-3-butynyl, 1-methyl-2-butynyl, 1,1-dimethyl-2-propynyl, 1-ethyl-2-propynyl, 2-hexynyl, 3-hexynyl, 4-hexynyl, 5-hexynyl, 1-methyl-2-pentynyl, 1-methyl-3-pentynyl, 1-methyl-4-pentynyl, 3-methyl-4-pentynyl, 4-methyl-2-pentynyl, 1,1-dimethyl-2-butynyl, 1,1-dimethyl-3-butynyl, 1,2-dimethyl-3-butynyl, 2,2-dimethyl-3-butynyl, 1-ethyl-2-butynyl, 1-ethyl-3-butynyl, 2-ethyl-3-butynyl and 1-ethyl-1-methyl-2-propynyl; C.sub.3 -C.sub.8 -cycloalkyl, such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and cyclooctyl, especially cyclopropyl and cyclohexyl; the abovementioned organic groups may bear from one to five halogen atoms, such as fluorine, chlorine, bromine and iodine, preferably fluorine, chlorine and bromine, and especially fluorine and chlorine, and/or from one to three of the following radicals: cyano; C.sub.3 -C.sub.8 -cycloalkyl, such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and cyclooctyl, especially cyclopropyl and cyclohexyl; C.sub.1 -C.sub.4 -alkoxy, such as methoxy, ethoxy, n-propoxy, 2-methylethoxy, n-butoxy, 1-methylpropoxy, 2-methylpropoxy and 1,1-dimethylethoxy, especially methoxy and ethoxy; C.sub.1 -C.sub.4 -haloalkoxy, such as chloromethoxy, dichloromethoxy, trichloromethoxy, fluoromethoxy, difluoromethoxy, trifluoromethoxy, chlorodifluoromethoxy, dichlorofluoromethoxy, 1-fluoroethoxy, 2-fluoroethoxy, 2,2-difluoroethoxy, 1,1,2,2-tetrafluoroethoxy, 2,2,2-trifluoroethoxy, 2-chloro-1,1,2-trifluoroethoxy and pentafluoroethoxy, especially 2,2,2-trifluoroethyloxy and 2-chloro-2,2-difluoroethoxy; C.sub.1 -C.sub.4 -alkylthio, such as methylthio, ethylthio, n-propylthio, 1-methylethylthio, n-butylthio, 1-methylpropylthio, 2-methylpropylthio and 1,1-dimethylethylthio, especially methylthio; C.sub.1 -C.sub.4 -haloalkylthio, such as difluoromethylthio, trifluoromethylthio, chlorodifluoromethylthio, 1-fluoroethylthio, 2-fluoroethylthio, 2,2-difluoroethylthio, 2,2,2-trifluoroethylthio, 2-chlor-2,2-difluoroethylthio, 2,2-dichloro-2-fluoroethylthio, 2,2,2-trichloroethylthio and pentafluoroethylthio, especially trichloromethylthio; phenyl, phenylthio, phenoxy, where the phenyl radicals in turn may bear from one to five halogen atoms such as fluorine, chlorine, bromine and iodine, especially fluorine and chlorine, and/or from one to three of the following groups: cyano or nitro; C.sub.1 -C.sub.4 -alkyl, as mentioned above, especially methyl, ethyl, propyl, 1-methylpropyl and 1,1-dimethylpropyl; C.sub.1 -C.sub.4 -alkoxy, as mentioned above, especially methoxy and ethoxy; C.sub.1 -C.sub.4 -haloalkyl, as mentioned above, especially trifluoromethyl; C.sub.1 -C.sub.4 -haloalkoxy, as mentioned above, especially trifluoromethoxy;

R.sup.2

hydrogen, hydroxy; C.sub.1 -C.sub.8 -alkoxy, e.g., methoxy, ethoxy, n-propoxy, 2-methylethoxy, n-butoxy, 1-methylpropoxy, 2-methylpropoxy and 1,1-dimethylethoxy, especially C.sub.1 -C.sub.4 -alkoxy such as methoxy, ethoxy, propoxy, butoxy; C.sub.3 -C.sub.8 -alkenyloxy, such as 2-propenyloxy, 2-butenyloxy, 3-butenyloxy, 1-methyl-2-propenyloxy, 2-methyl-2-propenyloxy, 2-pentenyloxy, 3-pentenyloxy, 4-pentenyloxy, 3-methyl-2-butenyloxy, 1-methyl-2-butenyloxy, 2-methyl-2-butenyloxy, 1-methyl-3-butenyloxy, 2-methyl-3-butenyloxy, 3-methyl-3-butenyloxy, 1,1-dimethyl-2-propenyloxy, 1,2-dimethyl-2-propenyloxy, 1-ethyl-2-propenyloxy, 2-hexenyloxy, 3-hexenyloxy, 4-hexenyloxy, 5-hexenyloxy, 1-methyl-2-pentenyloxy, 2-methyl-2-pentenyloxy, 3-methyl-2-pentenyloxy, 4-methyl-2-pentenyloxy, 1-methyl-3-pentenyloxy, 2-methyl-3-pentenyloxy, 3-methyl-3-pentenyloxy, 4-methyl-4-pentenyloxy, 1-methyl-4-pentenyloxy, 2-methyl-4-pentenyloxy, 3-methyl-4-pentenyloxy, 4-methyl-4-pentenyloxy, 1,1-dimethyl-2-butenyloxy, 1,1-dimethyl-3-butenyloxy, 1,2-dimethyl-2-butenyloxy, 1,2-dimethyl-3-butenyloxy, 1,3-dimethyl-2-butenyloxy, 1,3-dimethyl-3-butenyloxy, 2,2-dimethyl-3-butenyloxy, 2,3-dimethyl-2-butenyloxy, 2,3-dimethyl-4-butenyl, 1-ethyl-2-butenyl, 1-ethyl-3-butenyl, 2-ethyl-2-butenyloxy, 2-ethyl-3-butenyloxy, 1,1,2-trimethyl-2-propenyloxy, 1-ethyl-1-methyl-2-propenyloxy and ethyl-2-methyl-2-propenyloxy, especially 2-propenyloxy; di-C.sub.1 -C.sub.4 -alkylamino, C.sub.1 -C.sub.25 -alkyl, C.sub.3 -C.sub.25 -alkenyl and -alkynyl and C.sub.3 -C.sub.8 -cycloalkyl, as mentioned above generally and particularly for R.sup.1, and the abovementioned organic groups may bear from one to five halogen atoms such as fluorine, chlorine, bromine and iodine, preferably fluorine, chlorine and bromine, and especially fluorine and chlorine, and/or from one to three of the following radicals: cyano, C.sub.3 -C.sub.8 -cycloalkyl, C.sub.1 -C.sub.4 -alkoxy, C.sub.1 -C.sub.4 -haloalkoxy, C.sub.1 -C.sub.4 -alkylthio, C.sub.1 -C.sub.4 -haloalkylthio and di-C.sub.1 -C.sub.4 -alkylamino, each as mentioned individually above, phenyl, phenylthio, phenoxy, and the phenyl radicals in turn may bear from one to five halogen atoms such as fluorine, chlorine, bromine and iodine, especially fluorine and chlorine, and/or from one to three of the following groups: cyano or nitro, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -alkoxy, C.sub.1 -C.sub.4 -haloalkyl and C.sub.1 -C.sub.4 -haloalkoxy, each as mentioned above; R.sup.2 may further denote substituted C.sub.1 -C.sub.8 -alkoxy, C.sub.3 -C.sub.8 -alkenyloxy, di-C.sub.1 -C.sub.4 -alkylamino, C.sub.1 -C.sub.25 -alkyl, C.sub.3 -C.sub.25 -alkenyl, C.sub.3 -C.sub.25 -alkynyl or C.sub.3 -C.sub.8 -cycloalkyl, and these groups are substituted by from one to five halogen atoms and/or one or two 5- or 6-membered heterocyclic, aliphatic or aromatic radicals containing one to three heteroatoms selected from the group consisting of oxygen, sulfur and nitrogen; the following heterocyclic radicals are given by way of example: 2-tetrahydrofuranyl, 3-tetrahydrofuranyl, 2-tetrahydrothienyl, 3-tetrahydrothienyl, 2-tetrahydropyranyl, 3-tetrahydropyranyl, 4-tetrahydropyranyl, 2-furanyl, 3-furanyl, 2-thienyl, 3-thienyl, 3-isoxazolyl, 4-isoxazolyl, 5-isoxazolyl, 3-isothiazolyl, 4-isothiazolyl, 5-isothiazolyl, 2-oxazolyl, 4-oxazolyl, 5-oxazolyl, 2-thiazolyl, 4-thiazolyl, 5-thiazolyl, 2-imidazolyl, 4-imidazolyl, 5-imidazolyl, 2-pyrrolyl, 3-pyrrolyl, 3-pyrrolyl, 3-pyrazolyl, 4-pyrazolyl, 5-pyrazolyl, 2-pyridyl, 4-pyridyl, 4-pyridyl, oxa-2,4-diazolyl, oxa-3,4-diazolyl, thia-2,4-diazolyl, thia-3,4-diazolyl and triazolyl; and these heterocyclic radicals may bear one or two of the following substituents: halogen, such as fluorine, chlorine, bromine and iodine, especially fluorine and chlorine, C.sub.1 -C.sub.3 -alkyl or C.sub.1 -C.sub.3 -alkoxy, as mentioned above; R.sup.1 and R.sup.2 together denote a C.sub.4 -C.sub.7 -alkylene chain which may be interrupted by oxygen, sulfur or N-methyl, such as --(CH.sub.2).sub.3 --, --(CH.sub.2).sub.4 --, --(CH.sub.2).sub.5 --, --(CH.sub.2).sub.6 --, --CH.sub.2 --O--CH.sub.2 --, --CH.sub.2 --CH.sub.2 --O--CH.sub.2 --CH.sub.2 --, --CH.sub.2 --S--CH.sub.2 --, --CH.sub.2 --CH.sub.2 --S--CH.sub.2 -CH.sub.2 --, --CH.sub.2 --N(CH.sub.3)--CH.sub.2 --CH.sub.2 --, especially --(CH.sub.2).sub.5 -- and --CH.sub.2 --CH.sub.2 --O--CH.sub.2 --CH.sub.2 --;

R.sup.3 to R.sup.6

hydrogen; halogen, such as fluorine, chlorine, bromine and iodine, especially fluorine and chlorine; cyano or nitro; C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -alkoxy, C.sub.1 -C.sub.4 -haloalkyl, C.sub.1 -C.sub.4 -haloalkoxy, C.sub.1 -C.sub.4 -alkylthio or C.sub.1 -C.sub.4 -haloalkylthio, each as mentioned above individually for R.sup.1.

Examples of suitable salts of compounds I are agriculturally useful salts such as alkali metal salts, especially the potassium and sodium salts, alkaline earth metal salts, especially the calcium, magnesium and barium salts, manganese, copper, zinc or iron salts, and ammonium, phosphonium, tetraalkylammonium salts, benzyltrialkylammonium salts, trialkylsulfonium salts and trialkylsulfoxonium salts.

Examples of particularly preferred compounds of the formula I are given in the following table:

TABLE__________________________________________________________________________Compounds of the structure I ##STR7##R.sup.1 R.sup.2 R.sup.3 R.sup.4 R.sup.5 R.sup.6 X__________________________________________________________________________H 1,1-dimethyl-2-propenyl H H H H OH 2-propynyl H H H H OH 1-methyl-2-propynyl H H H H OH 1,1-dimethyl-2-propynyl H H H H OH benzyl H H H H OH 1-methyl-phenylmethyl H H H H OH 1,1-dimethylphenylmethyl H H H H OH 2-phenylethyl H H H H OH 2-methylthioethyl H H H H OH 1-methyl-2-methylthioethyl H H H H OH 1,1-dimethyl-2-methylthioethyl H H H H OH 2-fluoroethyl H H H H OH 2-fluoro-1-methylethyl H H H H OH 1,1-dimethyl-2-fluoroethyl H H H H OH 2-chloroethyl H H H H OH 2-chloro-1-methyl-ethyl H H H H OH 2-chloro-1,1-dimethylethyl H H H H OH 2-cyanoethyl H H H H OH 2-cyano-1,1-dimethylethyl H H H H OH dimethylamino H H H H OH 2-chlorobenzy1 H H H H OH 4-methoxybenzyl H H H H OH OH H H H H OH methoxy H H H H OH ethoxy H H H H OH propoxy H H H H OH 2-propenyloxy H H H H OH benzyloxy H H H H OH 2-phenoxyethyl H H H H OH H H Cl H H OH H H H H Cl OH H H methyl H H OH H H methoxy H H OH H H NO.sub.2 H H OH H H cyano H H OH tert.butyl F H H H OH tert.butyl H F H H OH tert.butyl H H F H OH tert.butyl H H H F OH isopropyl H H H F OH isopropyl H H F H OH isopropyl H F H H OH isopropyl F H H H OH tert.butyl methyl H H H OH isopropyl methyl H H H OH tert.butyl H methyl H H OH isopropyl H methyl H H OH tert.butyl H H methyl H OH isopropyl H H methyl H OH tert.butyl H methoxy methoxy H OH tert.butyl NO.sub.2 H NO.sub.2 H OH isopropyl NO.sub.2 H NO.sub.2 H OH tert.butyl methyl H Br H OH tert.butyl H 1,1,2,2-tetra- H H O fluoroethoxyH tert.butyl Cl H H H OH isopropyl Cl H H H OH tert.butyl methoxy methoxy methoxy H OH tert.butyl methyl Cl H H OH tert.butyl H NO.sub.2 H H OH tert.butyl Br H Br H OH tert.butyl H Cl H H OH tert.butyl H H methoxy H OH tert.butyl methyl methyl Br H OH tert.butyl NO.sub.2 H methyl H OH tert.butyl H H trifluo- H O romethylH tert.butyl Cl H Cl H OH isopropyl Cl H Cl H Omethyl methyl H H H H Omethyl isopropyl H H H H Omethyl ethyl H H H H Omethyl Cyclopropyl H H H H OBenzyl benzyl H H H H OH methyl H Cl H H OH ethyl H Cl H H OH propyl H Cl H H OH 2,2-dimethylbutyl H H H H OH 1,1-dimethylbutyl H H H H OH 1,1-dimethylpentyl H H H H OH cyclohexyl H H H H OH cyclopentyl H H H H OH 1,2,2,-trimethylpropyl H H H H OH 1-methylcyclopropyl H H H H OH cyclopropylmethyl H H H H OH 1-(cyclopropyl)-ethyl H H H H OH 1-methylcyclohexyl H H H H OH cyclohexylmethyl H H H H OH 2-propenyl H H H H OH 1-methyl-2-propenyl H H H H OH 1,1-dimethyl-2-propenyl H H H H SH 2-propynyl H H H H SH 1-methyl-2-propynyl H H H H SH 1,1-dimethyl-2-propynyl H H H H SH benzyl H H H H SH 1-methylphenylmethyl H H H H SH 1,1-dimethylphenylmethyl H H H H SH 2-phenylethyl H H H H SH 2-methylthioethyl H H H H SH 1-methyl-2-methylthioethyl H H H H SH 1,1-dimethyl-2-methylthioethyl H H H H SH 2-fluoroethyl H H H H SH 2-fluoro-1-methylethyl H H H H SH 1,1-dimethy1-2-fluoroethyl H H H H SH 2-chlorothyl H H H H SH 2-chloro-1-methylethyl H H H H SH 2-chloro-1,1-dimethylethyl H H H H SH 2-cyanoethyl H H H H SH 2-cyano-1,1-dimethylethyl H H H H SH dimethylamino H H H H SH 2-chlorobenzyl H H H H SH 4-methoxybenzyl H H H H SH OH H H H H SH methoxy H H H H SH ethoxy H H H H SH propoxy H H H H SH 2-propenyloxy H H H H SH benzyloxy H H H H SH 2-phenoxyethyl H H H H SH H H Cl H H SH H H H H Cl SH H H methyl H H SH H H methoxy H H SH H H NO.sub.2 H H SH H H cyano H H SH tert.butyl F H H H SH tert.butyl H F H H SH tert.butyl H H F H SH tert.butyl H H H F SH isopropyl H H H F SH isopropyl H H F H SH isopropyl H F H H SH isopropyl F H H H SH tert.butyl methyl H H H SH isopropyl methyl H H H SH tert.butyl H methyl H H SH isopropyl H methyl H H SH tert.butyl H H methyl H SH isopropyl H H methyl H SH tert.butyl H methoxy methoxy H SH tert.butyl NO.sub.2 H NO.sub.2 H SH isopropyl NO.sub.2 H NO.sub.2 H SH tert.bButyl methyl H Br H SH tert.butyl H 1,1,2,2-tetra- H H S fluoroethoxyH tert.butyl Cl H H H SH isopropyl Cl H H H SH tert.butyl methoxy methoxy methoxy H SH tert.butyl methyl Cl H H SH tert.butyt H NO.sub.2 H H SH tert.butyl Br H Br H SH tert.butyl H Cl H H SH tert.butyl H H methoxy H SH tert.butyl methyl methyl Br H SH tert.butyl NO.sub.2 H methyl H SH tert.butyl H H trifluo- H S romethylH tert.butyl Cl H Cl H SH isopropyl Cl H Cl H Smethyl methyl H H H H Smethyl isopropyl H H H H Smethyl ethyl H H H H Smethyl cyclopropyl H H H H Sbenzyl benzyl H H H H SH methyl H Cl H H SH ethyl H Cl H H SH propyl H Cl H H SH 2,2-dimethylbutyl H H H H SH 1,1-dimethylbutyl H H H H SH 1,1-dimethylpentyl H H H H SH cyclohexyl H H H H SH cyclopentyl H H H H SH 1,2,2-trimethylpropyl H H H H SH 1-methylcyclopropyl H H H H SH cyclopropylmethyl H H H H SH 1-(cyclopropyl)-ethyl H H H H SH 1-methylcyclohexyl H H H H SH cyclohexylmethyl H H H H SH 2-propenyl H H H H SH 1-methyl-2-propenyl H H H H S__________________________________________________________________________

The compounds I, or herbicidal agents containing them, may be applied for instance in the form of directly sprayable solutions, powders, suspensions (including high-percentage aqueous, oily or other suspensions), dispersions, emulsions, oil dispersions, pastes, dusts, broadcasting agents, or granules by spraying, atomizing, dusting, broadcasting or watering. The forms of application depend entirely on the purpose for which the agents are being used, but they must ensure as fine a distribution of the active ingredients according to the invention as possible.

For the preparation of solutions, emulsions, pastes and oil dispersions to be sprayed direct, mineral oil fractions of medium to high boiling point, such as kerosene or diesel oil, further coal-tar oils, and oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons such as toluene, xylene, paraffin, tetrahydronaphthalene, alkylated naphthalenes and their derivatives, methanol, ethanol, propanol, butanol, cyclohexanol, cyclohexanone, chlorobenzene, isophorone, etc., and strongly polar solvents such as N,N-dimethylformamide, dimethyl sulfoxide, N-methylpyrrolidone, water, etc. are suitable.

Aqueous formulations may be prepared from emulsion concentrates, pastes, oil dispersions, wettable powders or water-dispersible granules by adding water. To prepare emulsions, pastes and oil dispersions the ingredients as such or dissolved in an oil or solvent may be homogenized in water by means of wetting or dispersing agents, adherents or emulsifiers. Concentrates which are suitable for dilution with water may be prepared from active ingredient, wetting agent, adherent, emulsifying or dispersing agent and possibly solvent or oil.

Examples of surfactants are: alkali metal, alkaline earth metal and ammonium salts of aromatic sulfonic acids, e.g., ligninsulfonic acid, phenolsulfonic acid, naphthalenesulfonic acid and dibutylnaphthalenesulfonic acid, and of fatty acids, alkyl and alkylaryl sulfonates, and alkyl, lauryl ether and fatty alcohol sulfates, and salts of sulfated hexadecanols, heptadecanols, and octadecanols, salts of fatty alcohol glycol ethers, condensation products of sulfonated naphthalene and naphthalene derivatives with formaldehyde, condensation products of naphthalene or naphthalenesulfonic acids with phenol and formaldehyde, polyoxyethylene octylphenol ethers, ethoxylated isooctylphenol, ethoxylated octylphenol and ethoxylated nonylphenol, alkylphenol polyglycol ethers, tributylphenyl polyglycol ethers, alkylaryl polyether alcohols, isotridecyl alcohol, fatty alcohol ethylene oxide condensates, ethoxylated castor oil, polyoxyethylene alkyl ethers, ethoxylated polyoxypropylene, lauryl alcohol polyglycol ether acetal, sorbitol esters, lignin-sulfite waste liquors and methyl cellulose.

Powders, dusts and broadcasting agents may be prepared by mixing or grinding the active ingredients with a solid carrier.

Granules, e.g., coated, impregnated or homogeneous granules, may be prepared by bonding the active ingredients to solid carriers. Examples of solid carriers are mineral earths such as silicic acids, silica gels, silicates, talc, kaolin, attapulgus clay, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate, magnesium oxide, ground plastics, fertilizers such as ammonium sulfate, ammonium phosphate, ammonium nitrate, and ureas, and vegetable products such as grain meals, bark meal, wood meal, and nutshell meal, cellulosic powders, etc.

The formulations contain from 0.01 to 95, and preferably 0.5 to 90, % by weight of active ingredient. The active ingredients are used in a purity of from 90 to 100, and preferably from 95 to 100, % (according to the NMR spectrum).

The compounds I according to the invention may be formulated for example as follows:

I. 90 parts by weight of compound no. 1.01 is mixed with 10 parts by weight of N-methyl-.alpha.-pyrrolidone. A mixture is obtained which is suitable for application in the form of very fine drops. II. 20 parts by weight of compound no. 1.05 is dissolved in a mixture consisting of 80 parts by weight of xylene, 10 parts by weight of the adduct of 8 to 10 moles of ethylene oxide and 1 mole of oleic acid-N-monoethanolamide, 5 parts by weight of the calcium salt of dodecylbenzene-sulfonic acid, and 5 parts by weight of the adduct of 40 moles of ethylene oxide and 1 mole of castor oil. By pouring the solution into 100,000 parts by weight of water and uniformly distributing it therein, an aqueous dispersion is obtained containing 0.02% by weight of the active ingredient. III. 20 parts by weight of compound no. 1.01 is dissolved in a mixture consisting of 40 parts by weight of cyclohexanone, 30 parts by weight of isobutanol, 20 parts by weight of the adduct of 7 moles of ethylene oxide and 1 mole of isooctylphenol, and 10 parts by weight of the adduct of 40 moles of ethylene oxide and 1 mole of castor oil. By pouring the solution into 100,000 parts by weight of water and finely distributing it therein, an aqueous dispersion is obtained containing 0.02% by weight of the active ingredient. IV. 20 parts by weight of compound no. 1.05 is dissolved in a mixture consisting of 25 parts by weight of cyclohexanone, 65 parts by weight of a mineral oil fraction having a boiling point between 210.degree. and 280.degree. C., and 10 parts by weight of the adduct of 40 moles of ethylene oxide and 1 mole of castor oil. By pouring the solution into 100,000 parts by weight of water and uniformly distributing it therein, an aqueous dispersion is obtained containing 0.02% by weight of the active ingredient. V. 20 parts by weight of compound no. 1.01 is well mixed with 3 parts by weight of the sodium salt of diisobutylnaphthalene-.alpha.-sulfonic acid, 17 parts by weight of the sodium salt of a lignin-sulfonic acid obtained from a sulfite waste liquor, and 60 parts by weight of powdered silica gel, and triturated in a hammer mill. By uniformly distributing the mixture in 20,000 parts by weight of water, a spray liquor is obtained containing 0.1% by weight of the active ingredient. VI. 3 parts by weight of compound no. 1.01 is intimately mixed with 97 parts by weight of particulate kaolin. A dust is obtained containing 3% by weight of the active ingredient. VII. 30 parts by weight of compound no. 1.01 is intimately mixed with a mixture consisting of 92 parts by weight of powdered silica gel and 8 parts by weight of paraffin oil which has been sprayed onto the surface of this silica gel. A formulation of the active ingredient is obtained having good adherence. VIII. 20 parts by weight of compound no. 1.01 is intimately mixed with 2 parts of the calcium salt of dodecylbenzenesulfonic acid, 8 parts of a fatty alcohol polyglycol ether, 2 parts of the sodium salt of a phenolsulfonic acid-urea-formaldehyde condensate and 68 parts of a paraffinic mineral oil. A stable oily dispersion is obtained.

The active ingredients or the herbicidal agents containing them may be applied pre- or postemergence. If certain crop plants tolerate the active ingredients less well, application techniques may be used in which the herbicidal agents are sprayed from suitable equipment in such a manner that the leaves of sensitive crop plants are if possible not touched, and the agents reach the soil or the unwanted plants growing beneath the crop plants (post-directed, lay-by treatment).

The application rates depend on the objective to be achieved, the time of the year,. the plants to be combated and their growth stage, and are from 0.001 to 3, preferably 0.01 to 1, kg of active ingredient per hectare.

In view of the numerous application methods possible, the compounds according to the invention, or agents containing them, may be used in a large number of crops. Those which follow are given by way of example:

______________________________________Allium cepa onionsAnanas comosus pineapplesArachis hypogaea peanuts (groundnuts)Asparagus officinalis asparagusBeta vulgaris spp. altissima sugarbeetsBeta vulgaris spp. rapa fodder beetsBrassica napus var. napus rapeseedBrassica napus var. napobrassica swedesCamellia sinensis tea plantsCarthamus tinctorius safflowerCarya illinoinensis pecan treesCitrus limon lemonsCitrus sinensis orange treesCoffea arabica (Coffea canephora, coffee plantsCoffea liberica)Cucumis sativus cucumbersCynodon dactylon BermudagrassDaucus carota carrotsElais guineensis oil palmsFragaria vesca strawberriesGlycine max soybeansGossypium hirsutum (Gossypium cottonarboreum,Gossypium herbaceum,Gossypium vitifolium)Helianthus annuus sunflowersHevea brasiliensis rubber plantsHordeum vulgare barleyHumulus lupulus hopsIpomoea batatas sweet potatoesJuglans regia walnut treesLens culinaris lentilsLinum usitatissimum flaxLycopersicon lycopersicum tomatoesMalus spp. apple treesManihot esculenta cassavaMedicago sativa alfalfa (lucerne)Musa spp. banana plantsNicotiana tabacum (N. rustica) tobaccoOlea europaea olive treesOryza sativa ricePhaseolus lunatus limabeansPhaseolus vulgaris snapbeans, green beans, dry beansPicea abies Norway sprucePinus spp. pine treesPisum sativum English peasPrunus avium cherry treesPrunus persica peach treesPyrus communis pear treesRibes sylvestre redcurrantsRicinus communis castor-oil plantsSaccharum officinarum sugar caneSecale cereale ryeSolanum tuberosum Irish potatoesSorghum bicolor (s. vulgare) sorghumTheobroma cacao cacao plantsTrifolium pratense red cloverTriticum aestivum wheatTriticum durum wheatVicia faba tick beansVitis vinifera grapesZea mays Indian corn, sweet corn, maize______________________________________

To increase the spectrum of action and to achieve synergistic effects, the quinoline-3-carboxamides I may be mixed with each other, or mixed and applied together with numerous representatives of other herbicidal or growth-regulating active ingredient groups. Examples of suitable components are diazines, 4H-3,1-benzoxazine derivatives, benzothiadiazinones, 2,6-dinitroanilines, N-phenylcarbamates, thiolcarbamates, halocarboxylic acids, triazines, amides, ureas, diphenyl ethers, triazinones, uracils, benzofuran derivatives, cyclohexane-1,3-dione derivatives, quinolinecarboxylic acids, sulfonylureas, (hetero)-aryloxyphenoxypropionic acids and salts, esters, amides thereof, etc.

It may also be useful to apply the novel compounds I, either alone or in combination with other herbicides, in admixture with other crop protection agents, e.g., agents for combating pests or phytopathogenic fungi or bacteria. The compounds may also be mixed with solutions of mineral salts used to remedy nutritional or trace element deficiencies. Non-phytotoxic oils and oil concentrates may also be added.

SYNTHESIS EXAMPLES

Example 1

Preparation of 4-hydroxy-2-oxoquinoline-3-carboxylic Acid tert-butylamide

8.76 g (0.04 mol) of methyl 4-hydroxy-2-oxoquinoline-3-carboxylate was stirred with 3.7 g (0.05 mol) of tert-butylamine in 60 ml of ethanol in a miniautoclave for 8 hours at 150.degree. C. under autogenous pressure. After cooling, the crystals were removed by suction filtration, washed with ligroin and dried.

M.p.: 230.degree.-231.degree. C.; yield: 7.7 g (74% of theory).

Further compounds I were prepared analogously with appropriate modifications of the starting materials. The compounds thus obtained are listed with their physical data in Table 1 below.

TABLE 1__________________________________________________________________________Quinoline-3-carboxamides of the structure I; X = O ##STR8## Phys. dataNo. R.sup.1 R.sup.2 R.sup.3 R.sup.4 R.sup.5 R.sup.6 m.p. .degree.C.__________________________________________________________________________1.01 H tert.-butyl H H H H 2301.02 H isopropyl H H H H 2431.03 H 1-methylpropyl H H H H 2061.04 H 2-methylpropyl H H H H 2251.05 H 1-ethylpropyl H H H H 2051.06 H 1,1,2-trimethylpropyl H H H H 269-2701.07 H 2-methoxy-1-methylethyl H H H H 2001.08 H 2-methoxy-1-ethylethyl H H H H 168-1701.09 H 1-ethyl-1-methylpentyl H H H H 148-1501.10 H 2-methylbutyl H H H H 177-1801.11 H n-heptyl H H H H 1501.12 H n-octyl H H H H 1461.13 H n-nonyl H H H H 1471.14 H n-decyl H H H H 1521.15 H n-undecyl H H H H 1381.16 H n-dodecyl H H H H 1301.17 H n-tridecyl H H H H 1321.18 H n-tetradecyl H H H H 1181.19 H n-pentadecyl H H H H 1201.20 H cyclopropyl H H H H 2701.21 H tert.-butyl H Cl H H 295-2981.22 H isopropyl H Cl H H 305-3101.23 H tert.-butyl H H H Cl 287-2911.24 H isopropyl H H H Cl 280-2851.25 H tert.-butyl methyl H H H >2201.26 H isopropyl methyl H H H >2201.27 H vyclopropyl methyl H H H >2201.28 H 1,1-dimethylpropynyl methyl H H H 2551.29 H 1-cyclopropylethyl methyl H H H 2691.30 H 1,1-dimethylpropenyl methyl H H H 2381.31 H 1-(methoxymethyl)-ethyl methyl H H H 2131.32 H tert.-butyl H H H F 3031.33 H isopropyl H H H F 2921.34 H cyclopropyl H H H F 3051.35 H 1,1-dimethylpropenyl H H H F 2651.36 H 1-cyclopropylethyl H H H F 2041.37 H 1-(methoxymethyl)-ethyl H H H F 2351.38 H tert.-butyl H F H H 2801.39 H isopropyl H F H H 2951.40 H cyclopropyl H F H H 3121.41 H 1-(methoxymethyl)-ethyl H F H H 2261.42 H 1,1-dimethylpropenyl H F H H 2611.43 H 1-cyclopropylethyl H F H H 2571.44 H tert.-butyl H H H methyl 2581.45 H isopropyl H H H methyl 2751.46 H tert.-butyl H methoxy methoxy H 3371.47 H cyclopropyl H H H methyl 2661.48 H 1-(methoxymethyl)-ethyl H H H methyl 173-1751.49 H tert.-butyl methyl H H methyl 222-2241.50 H isopropyl methyl H H methyl 251-2541.51 H tert.-butyl H H F H 273-2771.52 H isopropyl H H F H 274-2801.53 H tert.-butyl H methyl H H 287-2921.54 H cyclopropyl H H F H 306-3111.55 H isopropyl H methyl H H 248-2551.56 H 1-(methoxymethyl)-ethyl H H F H 214-2161.57 H cyclopropyl H methyl H H 289-2931.58 H 1,1-dimethylpropenyl H H F H 243-2481.59 H 1-(methoxymethyl)-ethyl H methyl H H 204-2071.60 H 1-cyclopropylethyl H H F H 213-2211.61 H 1,1-dimethylpropenyl H methyl H H 265-2711.62 H 1,1-dimethylpropenyl H H H methyl 230-2341.63 H 1-cyclopropylethyl H methyl H H 258-2621.64 H 1-cyclopropylethyl H H H methyl 180-1851.65 H tert.-butyl H H Cl H 303-3081.66 H isopropyl H H Cl H 285-2921.67 H cyclopropyl H H Cl H 221-2271.68 H 1-cyclopropylethyl H H Cl H 269-2721.69 H 1-(methoxymethyl)-ethyl H H Cl H 222-2281.70 H 1,1-dimethylpropenyl H H Cl H 294-3001.71 H tert.-butyl H H Br H 312-3161.72 H isopropyl H H Br H 278-2821.73 H cyclopropyl H H Br H 304-3091.74 H tert.-butyl H H methyl H 269-2751.75 H isopropyl H H methyl H 242-2471.76 H cyclopropyl H H methyl H 297-3051.77 H 1-cyclopropylethyl H H methyl H 235-2401.78 H 1-(methoxymethyl)-ethyl H H methyl H 201-2061.79 H 1,1-dimethylpropenyl H H methyl H 256-2601.80 H 1,1-dimethylethyl H H Br H 279-2821.81 H 1-(methoxymethyl)-ethyl H H Br H 228-2311.82 H 1,1-dimethylpropenyl H H Br H 299-3051.83 H tert.-butyl H H methoxy H 288-2921.84 H isopropyl H H methoxy H 278-2841.85 H 1-cyclopropylethyl H H methoxy H 269-2751.86 H 1-(methoxymethyl)-ethyl H H methoxy H 236-2411.87 H 1-(3-thienyl)-ethyl H H H F 253-2581.88 H 1-phenylethyl H H H F 240-2451.89 H tert.-butyl Cl H Cl H 259-2661.90 H isopropyl Cl H Cl H 250-2561.91 H 1-cyclopropylethyl Cl H Cl H 237-2411.92 H 1-(methoxymethyl)-ethyl Cl H Cl H 185-1901.93 H tert.-butyl H H I H 296-3021.94 H 1-cyclopropylethyl H H I H 265-2701.95 H 1-(methoxymethyl)-ethyl H H I H 249-2551.96 H isopropyl H H I H 289-294__________________________________________________________________________

Example 2

Preparation of 5-fluoro-4-hydroxy-2-oxoquinoline-3-carboxylic Acid-tert.-butylamide, Na Salt

6.0 g (0.023 mol) of 5-fluoro-4-hydroxy-2-oxoquinoline-3-carboxylic acid-tert.-butylamide is suspended in methanol, and a solution of 1.25 g of sodium methylate in methanol is added. The solution is stirred for 1 hour at room temperature and then evaporated down, and the residue is dried.

M.p.: >399.degree. C.; yield: 6.4 g, (98% of theory)

Further salts of compounds I were prepared with appropriate modification of the starting materials. The salts thus obtained are listed with their physical data in Table 2 below.

TABLE 2__________________________________________________________________________Salts of compounds of the structure I ##STR9## Phys. dataNo. R.sup.1 R.sup.2 R.sup.3 R.sup.4 R.sup.5 R.sup.6 Counterion m.p. .degree.C.__________________________________________________________________________2.01 H tert.-butyl H H H F Na.sup.+ 287-2972.02 H tert.-butyl H H H H K.sup.+ 332-3372.03 H 1-cyclopropylethyl H H H F K.sup.+ 290-2952.04 H 1-cyclopropylethyl H H H F Na.sup.+ 280-2972.05 H tert.-butyl H H H H Na.sup.+ 295-3002.06 H tert.-butyl H H H H K.sup.+ 289-2962.07 H tert.-butyl H H H H N(CH.sub.3).sub.4 .sup.+ .sup.1 H-NMR(DMSO) .delta.: 11.13(s, 1H), 9.98(s,1H), 7.80(d, 1H), 7.29(t, 1H), 7.06(d, 1H), 6.92(t, 1H), 3.21(s, 12H), 1.35(s, 9H)2.08 H tert.-butyl H H H H N(C.sub.2 H.sub.5).sub.4 .sup.+ .sup.1 H-NMR(DMSO) .delta.: 11.12(s, 1H), 9.98(s, 1H), 7.81(d, 1H), 7.29(t, 1H), 7.06(d, 1H), 6.95(t, 1H), 3.23(q, 6H); 1.35(s, 9H), 1.15(t, 10H)2.09 H tert.-butyl H H H H N(n-C.sub.4 H.sub.9).sub.4 .sup.+ .sup.1 H NMR(DMSO) .delta.: 11.10(s, 1H), 9.98(s, 1H), 7.90(d, 1H), 7.31(t, 1H), 7.08(d, 1H), 6.95(t, 1H), 3.18(m, 8H), 1.55(m, 8H), 1.35(s, 9H), 1.28(m, 8H), 0.95(t, 12H)__________________________________________________________________________

Example 3

The quinoline-3-carboxylates as intermediates for the synthesis of the corresponding amides were prepared as disclosed in Australian Journal of Chem. Vol. 7, P. 348 and 368 (1954).

Selected examples are given in Table 3.

TABLE 3______________________________________Intermediates of the formula ##STR10## Phys. dataNo. Y R.sup.3 R.sup.4 R.sup.5 R.sup.6 m.p. .degree.C.______________________________________3.01 methoxy H H H F >3993.02 methoxy H F H H 2453.03 methoxy H H H methyl 2503.04 methoxy H methyl H H 2353.05 methoxy H H F H 271-2743.06 methoxy H H Cl H 255-2593.07 methoxy H H Br H 257-2613.08 methoxy H H methyl H 236-2443.09 methoxy H methoxy methoxy H 329-3343.10 methoxy H H methoxy H 229-2373.12 methoxy methyl H H methyl 252-2553.12 methoxy H H I H >399______________________________________

USE EXAMPLES

The herbicidal action of compounds I is demonstrated in greenhouse experiments:

The vessels employed were plastic flowerpots filled with a sandy loam containing about 3.0% humus. The seeds of the test plants were sown separately, according to species.

For the preemergence treatment, the formulated active ingredients were applied to the surface of the soil immediately after the seeds had been sown. The compounds were emulsified or suspended in water as vehicle, and sprayed through finely distributing nozzles.

After the agents had been applied, the vessels were lightly sprinkler-irrigated to induce germination and growth.

Transparent plastic covers were then placed on the vessels until the plants had taken root. The cover ensured uniform germination of the plants, insofar as this was not impaired by the active ingredients.

For the postemergence treatment, the plants were grown, depending on growth form, to a height of 3 to 15 cm before being treated with the compounds, suspended or emulsified in water. The application rate for postemergence treatment was 3 kg/ha.

The pots were set up in the greenhouse at temperatures specific to their species--at from 20.degree. to 35.degree. C., or from 10.degree. to 25.degree. C. The experiments were run for from 2 to 4 weeks.

During this period the plants were tended and their reactions to the various treatments assessed. The assessment scale was 0 to 100, 100 denoting nonemergence or complete destruction of at least the visible plant parts, and 0 denoting no damage or normal growth.

The plants used in the greenhouse experiments were Echinochloa crus-galli and Centaurea cyanus.

Compounds 1.01 and 1.05, applied postemergence at a rate of 3 kg/ha, have a very good herbicidal action.

Claims

1. A quinoline-3-carboxamide of the formula ##STR11## wherein R.sup.1 is hydrogen,

R.sup.2 is tert.-butyl,

R.sup.3 is hydrogen,

R.sup.4 is hydrogen,

R.sup.5 is hydrogen,

R.sup.6 is hydrogen, and

X is oxygen.