CA2210909A1 - Novel 3-(4-cyanophenyl)uracils - Google Patents

Abstract

The invention concerns 3-(4-cyanophenyl)uracils of formula (I), wherein A = H, CH3, NH2; Y = -O-, -S-; R1 = H, halogen; R2 = H, halogen, C1-C6-alkyl, C1-C6-alkyl halide, C1-C6-alkylthio, C1-C6-alkylsulphenyl, C1-C6-alkylsulphonyl; R3 = H, halogen, C1-C6-alkyl; R4 = H, C1-C6-alkyl halide, C1-C6-alkyl, C3-C8-cycloalkyl, C3-C6-alkenyl, C3-C6-alkinyl, (C1-C6-alkyl)carbonyl, (C3-C6-alkenyl)carbonyl, (C3-C6-alkinyl)carbonyl or alkylsulphonyl, each of the last-mentioned eight groups being able to carry one to three substituents: halogen, nitro, cyamo, hydroxy, C3-C8-cycloalkyl, C1-C6-alkoxy, C3-C8-cycloalkoxy, C3-C6-alkenyloxy, C3-C6-alkinyloxy, C1-C6-alkoxy-C1-C6-alkoxy, C1-C6-alkylthio, C1-C6-alkylsulphenyl, C1-C6-alkylsulphonyl, C1-C6-alkylidene aminoxy, optionally substituted phenyl, phenoxy or phenylsulphonyl, an optionally substituted 3 to 7-member heterocyclyl or heterocyclyloxy group with one to three heteroatoms, -CO-XR5, OCO-XR5 or -N(R5)R6, wherein X = chemical bond, oxygen, sulphur or -N(R6)-; R5 = H, C1-C6-alkyl, C3-C8-cycloalkyl, C3-C6-alkenyl, C1-C6-alkinyl, C1-C6-alkoxy-C1-C6-alkyl, (C1-C6-alkoxy)carbonyl-C1-C6-alkyl, optionally substituted phenyl or phenyl-C1-C6-alkyl; or X and R5 together equal a 3 to 7-member heterocuclic ring which is bonded via nitrogen, has one to three heteroatoms and can optionally carry one to three substituents; R6 = H, OH, C1-C6-alkyl, C3-C8-cycloalkyl or C1-C6-alkoxy, and the salts of I whrn A = hydrogen. The products are used as herbicides, for dessiccating an defoliating plants.

Description

Novel 3-(4-cyanophenyl)uracils The present invention relates to novel 3-(4-cyanophenyl)uracils 5 of the general formula I

A o Rl N~ ~ CN
~ ~
R3 Y oR4 where the variables have the following -Anings:
A is hydrogen, methyl or amino;

Y is oxygen or sulfur;

20 Rl is hydrogen or halogen;

R2 is hydrogen, halogen, Cl-C6-alkyl, Cl-C6-haloalkyl, Cl-C6-alkylthio, Cl-C6-alkylsulfenyl or Cl-C6-alkylsulfonyl;

25 R3 is hydrogen, halogen or Cl-C6-alkyl;

R4 is hydrogen, Cl-C6-haloalkyl, Cl-C6-alkyl, C3 -C8-cyclo-alkyl, C3-C6-alkenyl, C3-C6-alkynyl, (Cl-C6-alkyl)-carbonyl, (C3-C6-alkenyl)carbonyl, (C3-C6-alkynyl)carbonyl or alkylsulfonyl, it being possible, if desired, for each of the last-mentioned 8 radicals to have attached to it one to three substituents, in each case selected from the group consisting of - halogen, nitro, cyano, hydroxyl, C3-C8-cycloalkyl, C1-C6-alkoxy, C3-C8-cycloalkoxy, C3-C6-alkenyloxy, C3-C6-alkynyloxy, Cl-C6-alkoxy-Cl-C6-alkoxy, Cl-C6-alkylthio, Cl-C6-alkylsulfenyl, Cl-C6-alkylsulfonyl, Cl-C6-alkylideneaminoxy, - the phenyl, phenoxy or phenylsulfonyl group which can be unsubstituted or have attached to it one to three substituents, in each case selected from the group consisting of halogen, nitro, cyano, Cl-C6-alkyl, Cl-C6-alkoxy and Cl-C6-haloalkyl, - a 3- to 7-membered heterocyclyl or heterocyclyloxy group having one to three hetero atoms selected from the group consisting of two oxygen atoms, two sulfur atoms and 3 nitrogen atoms, it being possible for the heterocycle to be saturated, partially or fully unsaturated or aromatic and, if desired, to have attached to it one to three substituents, in each case selected from the group consisting of halogen, nitro, cyano, C1-C6-alkyl, Cl-C6-alkoxy, C1-C6-haloalkyl and (C1-C6-alkyl)carbonyl, - a group -Co-XR5, -oCo-XR5 or -N(R5)R6 where X is a chemical bond, oxygen, sulfur or -N(R6)-;

15 R5 is hydrogen, Cl-C6-alkyl, C3-C8-cycloalkyl, C3-C6-alkenyl, C3-C6-alkynyl, Cl-C6-alkoxy-Cl-C6-alkyl, (C1-C6-alkoxy)-carbonyl-Cl-C6-alkyl, phenyl or phenyl-Cl-C6-alkyl, it being possible for the phenyl group and the phenyl ring of the phenylalkyl group to be unsub~tituted or to have attached to it one to three radicals, in each case selected from the group consisting of halogen, nitro, cyano, Cl-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy and (Cl-C6-alkyl)carbonyl X and Rs together form a 3- to 7-membered heterocycle, bonded via nitrogen and having one to three hetero atoms selected from the group consisting of two oxygen atomR, two sulfur atoms and 3 nitrogen atoms, it being possible for the heterocycle to be saturated, partially or fully unsaturated or aromatic and, if desired, to have attached to it one to three ~ubstituentQ, in each case selected from the group consisting of halogen, nitro, cyano, Cl-C6-alkyl, Cl-C6-haloalkyl Cl-C6-alkoxy and ~Cl-C6-alkyl)carbonyl;
and R6 represents hydrogen, hydroxyl, Cl-C6-alkyl, C3-C8-cycloalkyl or Cl-C6-alkoxy, and the agriculturally useful salt~ of those compounds I
where A is hydrogen.

The invention furthermore relates to - the use of the compounds I as herbicides and/or for the desiccation and/or defoliation of plants, - herbicidal compositions and compositions for desiccating and/or defoliating plants which comprise the compounds I as active ingredients, - methods of controlling undesirable vegetation and for desiccating and/or defoliating plants using the compounds I, - processes for the preparation of the compounds I and of herbicidal compositions and compositions for desiccating and/or defoliating plants using the compounds I, and 15 - novel intermediates of the formulae III and IV from which the compounds I are obtainable.

Regarding the compounds I where A - hydrogen or methyl, EP-A 255 047 is of particular importance since it discloses quite 20 generally 3-aryluracils of the formula II

Ra o Rl Rb ~ N ~ Rd II
R3~ O RC

where Ra is hydrogen, C1_4-alkyl, C1_4-haloalkyl, formyl or 30 C2_6-alkanoyl, Rb is C1_4-alkyl or C1_4-haloalkyl, R3~ is hydrogen, halogen or C1-C4-alkyl, Rc is an ether group or a radical R-CO-O-, R-CS-O- or R-SO2-O- and Rd is halogen or cyano 35 and the salts of the compounds II where Ra = hydrogen, as herbicides.

Examples of ~-phenyluracils in which the phenyl ring carries a cyano group para to the uracil radical (Rd)~ and their herbicidal 40 action, however, are not revealed by this document.

Certain l-amino-3-phenyluracils which, however, do not carry a cyano group on the phenyl ring have already been disclosed as herbicides in EP-A-517 181 and JP-A 05/025 143.

However, the herbicidal or desiccant/defoliant properties of the known compounds are not always entirely satisfactory.

It was therefore an object of the present invention to provide 5 novel, in particular herbicidally active compounds, which allow better, tailored control of undesirable plants than this was possible to date.

The object also extends to the provision of novel compounds which 10 act as desiccants/defoliants.

We have found that this object is achieved by the 3-(4-cyanophenyl)uracils of the formula I and their herbicidal action.
There have furthermore been found herbicidal compositions which comprise the compounds I and have a very good herbicidal action.
There have also been found processes for preparing these compositions and methods of controlling undesirable vegetation 20 using the compounds I.

It has furthermore been found that the compounds I are also suitable for defoliating and desiccating parts of plants, suitable plants being crop plants such as cotton, potatoes, 25 oilseed rape, sunflowers, soybeans or field beans, in particular cotton. Thus, there have been found compositions for the desiccation and/or defoliation of plants, processes for the preparation of these compositions, and methods of desiccating and/or defoliating plants using the compounds I.
Depending on the substitution pattern, the compounds of the formula I can have one or more chiral centers, in which case they are present as enantiomer or diastereomer mixtures. The invention relates to the pure enantiomers or diastereomers and to their 35 mixtures.

If A is hydrogen, the 3-(4-cyanophenyl)uracils I can be present in the form of their agriculturally useful salts, the type of salt not being critical, as a rule. In general, suitable salts 40 are salts of those bases which do not adversely affect the herbicidal action in comparison with the free compounds I.

Particularly suitable basic salts are those of the alkali metals, preferably sodium and potassium salts, of the alkaline earth 45 metals, preferably calcium and magnesium salts, those of the transition metals, preferably zinc and iron salts, and also ammonium salts where, if desired, the ammonium ion can have ' ' 0050/45615 attached to it one to three Cl-C4-alkyl or hydroxy-Cl-C4-alkyl substituents and/or a phenyl or benzyl substituent, preferably diisopropylammonium, tetramethylammonium, tetrabutylammonium, trimethylbenzylammonium and trimethyl(2-hydroxyethyl)ammonium 5 salts, furthermore phosphonium 6alts, sulfonium salts, such as, preferably, tri(Cl-C4-alkyl)sulfonium salts, and sulfoxonium salts, such as, preferably, tri(Cl-C4-alkyl)sulfoxonium salts.

The organic moieties mentioned for the substituents Rl to R6 or as 10 radicals on phenyl rings or heterocycles are - like the meaning halogen - collective terms for individual enumerations of the individual group members. All carbon chains, ie. all alkyl, haloalkyl, alkoxy, alkylthio, alkylsulfenyl, alkylsulfonyl, alkylcarbonyl, alkenyl, alkenyloxy, alkenylcarbonyl, alkynyl, 15 alkynyloxy, alkynylcarbonyl and alkylideneaminoxy moieties can be straight-chain or branched. Unless otherwise indicated, halogenated substituents preferably have attached to them one to five identical or different halogen atoms.

20 Examples of individual meanings are:

- halogen: fluorine, chlorine, bromine or iodine;

- Cl-C4-alkyl and the alkyl moieties of Cl-C6-alkoxy-Cl-C6-alkyl and ( Cl-C6 - alkoxy)carbonyl-Cl-C6-alkyl:
methyl, ethyl, n-propyl, 1-methylethyl, n-butyl, l-methylpropyl, 2-methylpropyl, 1,1-dimethylethyl, n-pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 2,2-dimethylpropyl, l-ethylpropyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, n-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, 2-ethylbutyl, 1,1,2-trimethylpropyl, 1,2,2-trimethylpropyl, 1-ethyl-1-methylpropyl or 1-ethyl-2-methylpropyl;

- Cl-C6-haloalkyl: a Cl-C6 - alkyl radical as mentioned above which is partially or fully substituted by fluorine, chlorine, bromine and/or iodine, eg. chloromethyl, dichloro-methyl, trichloromethyl, fluoromethyl, difluoromethyl, trifluoromethyl, chlorofluoromethyl, dichlorofluoromethyl, chlorodifluoromethyl, 2-fluoroethyl, 2-chloroethyl, 2-bromo-ethyl, 2-iodoethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl, 2-chloro-2-fluoroethyl, 2-chloro-2,2-difluoroethyl, 2,2-dichloro-2-fluoroethyl, 2,2,2-trichloroethyl, penta-fluoroethyl, 2-fluoropropyl,3-fluoropropyI, 2,2-difluoro-propyl, 2,3-difluoropropyl, 2-chloropropyl, 3-chloropropyl, 2,3-dichloropropyl, 2-bromopropyl, 3-bromopropyl, 3,3,3-tri-fluoropropyl, 3,3,3-trichloropropyl, 2,2,3,3,3-pentafluoro-propyl, heptafluoropropyl, l-(fluoromethyl)-2-fluoroethyl, 1-(chloromethyl)-2-chloroethyl, 1-(bromomethyl)-2-bromoethyl, 4-fluorobutyl, 4-chlorobutyl, 4-bromobutyl, nonafluorobutyl, 5-fluoropentyl, 5-chloropentyl, 5-bromopentyl, 5-iodopentyl, undecafluoropentyl, 6-fluorohexyl, 6-chlorohexyl, 6-bromo-hexyl, 6-iodohexyl or dodecafluorohexyl;

10 - phenyl-C1-C6-alkyl: eg. benzyl, l-phenylethyl, 2-phenylethyl, 1-phenylprop-1-yl, 2-phenylprop-1-yl, 3-phenylprop-1-yl, 1-phenylbut-1-yl, 2-phenylbut-1-yl, 3-phenylbut-l-yl, 4-phenylbut-1-yl, 1-phenylbut-2-yl, 2-phenylbut-2-yl, 3-phenylbut-2-yl, 3-phenylbut-2-yl, 4-phenylbut-2-yl, 1-(phenylmethyl)eth-1-yl, 1-(phenylmethyl)-1-(methyl)eth-1-yl and 1-(phenylmethyl)prop-1-yl, preferably benzyl, 2-phenyl-ethyl and 2-phenylhex-6-yl;

- C3-C6-alkenyl and the alkenyl moieties of C3-C6-alkenyloxy and (C3-C6-alkenyl)carbonyl: prop-1-en-1-yl, prop-2-en-1-yl, 1-methylethenyl, n-buten-l-yl, n-buten-2-yl, n-buten-3-yl, 1-methylprop-1-en-1-yl, 2-methylprop-l-en-1-yl, l-methyl-prop-2-en-1-yl or 2-methylprop-2-en-1-yl, n-penten-1-yl, n-penten-2-yl, n-penten-3-yl, n-penten-4-yl, 1-methylbut-1-en-l-yl, 2-methylbut-1-en-l-yl, 3-methylbut-1-en-1-yl, 1-methylbut-2-en-1-yl, 2-methylbut-2-en-1-yl, 3-methylbut-2-en-l-yl, 1-methylbut-3-en-1-yl, 2-methylbut-3-en-1-yl, 3-methylbut-3-en-1-yl, 1,1-dimethylprop-2-en-1-yl, 1,2-dimethylprop-1-en-1-yl, 1,2-dimethylprop-2-en-1-yl, l-ethylprop-1-en-2-yl, 1-ethylprop-2-en-1-yl, n-hex-1-en-l-yl, n-hex-2-en-l-yl, n-hex-3-en-1-yl, n-hex-4-en-1-yl, n-hex-5-en-1-yl, 1-methylpent-1-en-1-yl, 2-methylpent-1-en-1-yl, 3-methylpent-1-en-1-yl, 4-methylpent-1-en-1-yl, ' 1-methylpent-2-en-1-yl, 2-methylpent-2-en-1-yl, 3-methylpent-2-en-1-yl, 4-methylpent-2-en-1-yl, 1-methylpent-3-en-1-yl, 2-methylpent-3-en-1-yl, 3-methylpent-3-en-l-yl, 4-methylpent-3-en-1-yl, 1-methylpent-4-en-1-yl, 2-methylpent-4-en-1-yl, 3-methylpent-4-en-1-yl, 4-methylpent-4-en-1-yl, l,l-dimethyl-but-2-en-1-yl, 1,1-dimethylbut-3-en-1-yl, 1,2-dimethylbut-l-en-l-yl, 1,2-dimethylbut-2-en-1-yl, 1,2-dimethylbut-3-en-l-yl, 1,3-dimethylbut-1-en-1-yl, 1,3-dimethylbut-2-en-1-yl, 1,3-dimethylbut-3-en-1-yl, 2,2-dimethylbut-3-en-1-yl, 2,3-dimethylbut-l-en-1-yl, 2,3-dimethylbut-2-en-1-yl, 2,3-dimethylbut-3-en-1-yl, 3,3-dimethylbut-1-en-1-yl, 3,3-dimethylbut-2-en-l-yl, l-ethylbut-l-en-l-yl, l-ethylbut-2-en-1-yl, 1-ethylbut-3-en-l-yl, 2-ethylbut-1-en-1-yl, 2-ethylbut-2-en-l-yl, 2-ethylbut-3-en-1-yl, 1,1,2-trimethyl-CA 022l0909 l997-07-30 prop-2-en-1-yl, 1-ethyl-1-methylprop-2-en-1-yl, l-ethyl-2-methylprop-1-en-1-yl or 1-ethyl-2-methylprop-2-en-1-yl;

- C3-C6-alkynyl and the alkynyl moieties of C3-C6-alkynyloxy and (C3-C6-alkynyl)carbonyl: prop-1-yn-1-yl, prop-2-yn-1-yl, but-1-yn-1-yl, but-1-yn-3-yl, but-1-yn-4-yl, but-2-yn-1-yl, pent-1-yn-1-yl, n-pent-1-yn-3-yl, n-pent-1-yn-4-yl, n-pent-l-yn-5-yl, n-pent-2-yn-1-yl, n-pent-2-yn-4-yl, n-pent-2-yn-5-yl, 3-methylbut-1-yn-3-yl, 3-methylbut-1-yn-4-yl, n-hex-l-yn-l-yl, n-hex-1-yn-3-yl, n-hex-1-yn-4-yl, n-hex-l-yn-S-yl, n-hex-1-yn-6-yl, n-hex-2-yn-1-yl, n-hex-2-yn-4-yl, n-hex-2-yn-5-yl, n-hex-2-yn-6-yl, n-hex-3-yn-1-yl, n-hex-3-yn-2-yl, 3-methylpent-1-yn-1-yl, 3-methylpent-1-yn-3-yl, 3-methylpent-1-yn-4-yl, 3-methylpent-1-yn-5-yl, 4-methylpent-1-yn-1-yl, 4-methylpent-2-yn-4-yl or 4-methyl-pent-2-yn-5-yl;

- Cl-C6-alkoxy and the alkoxy moieties of Cl-C6-alkoxy-Cl-C6-alkyl and (C1-C6-alkoxy)carbonyl-Cl-C6-alkyl: methoxy, ethoxy, n-propoxy, l-methylethoxy, n-butoxy, l-methylpropoxy, 2-methylpropoxy or l,1-dimethyl-ethoxy, n-pentoxy, l-methylbutoxy, 2-methylbutoxy, 3-methyl-butoxy, l,1-dimethylpropoxy, 1,2-dimethylpropoxy, 2,2-dimethylpropoxy, l-ethylpropoxy, n-hexoxy, l-methyl-pentoxy, 2-methylpentoxy, 3-methylpentoxy, 4-methylpentoxy, 1,1-dimethylbutoxy,1,2-dimethylbutoxy, 1,3-dimethylbutoxy, 2,2-dimethylbutoxy, 2,3-dimethylbutoxy, 3,3-dimethylbutoxy, l-ethylbutoxy, 2-ethylbutoxy, 1,1,2-trimethylpropoxy, 1,2,2-trimethylpropoxy, l-ethyl-l-methylpropoxy or l-ethyl-2-methylpropoxy;

- Cl-C6-alkylthio: methylthio, ethylthio, n-propylthio, l-methylethylthio, n-butylthio, 1-methylpropylthio, 2-methylpropylthio, l,l-dimethylethylthio, n-pentylthio, l-methylbutylthio, 2-methylbutylthio, 3-methylbutylthio, 2,2-dimethylpropylthio, l-ethylpropylthio, n-hexylthio, 1,1-dimethylpropylthio, 1,2-dimethylpropylthio, 1-methylpentylthio, 2-methylpentylthio, 3-methylpentylthio, 4-methylpentylthio, l,l-dimethylbutylthio, 1,2-dimethylbutylthio, 1,3-dimethylbutylthio, 2,2-dimethylbutylthio, 2,3-dimethylbutylthio, 3,3-dimethylbutylthio, l-ethylbutyl-thio, 2-ethylbutylthio, 1,1,2-trimethylpropylthio, 1,2,2-trimethylpropylthio, 1-ethyl-1-methylpropylthio or 1-ethyl-2-methylpropylthio;

- (Cl-C6-alkyl)carbonyl: methylcarbonyl, ethylcarbonyl, n-propylcarbonyl, l-methylethylcarbonyl, n-butylcarbonyl, l-methylpropylcarbonyl, 2-methylpropylcarbonyl, l,l-dimethylethylcarbonyl, n-pentylcarbonyl, 1-methylbutylcarbonyl, 2-methylbutylcarbonyl, 3-methylbutylcarbonyl, l,1-dimethylpropylcarbonyl, 1,2-dimethylpropylcarbonyl, 2,2-dimethylpropylcarbonyl, l-ethylpropylcarbonyl, hexylcarbonyl, l-methylpentylcarbonyl, 2-methylpentylcarbonyl, 3-methylpentylcarbonyl, 4-methylpentylcarbonyl, l,l-dimethylbutylcarbonyl, 1,2-dimethylbutylcarbonyl, 1,3-dimethylbutylcarbonyl, 2,2-dimethylbutylcarbonyl, 2,3-dimethylbutylcarbonyl, 3,3-dimethylbutylcarbonyl, l-ethylbutylcarbonyl, 2-ethylbutylcarbonyl, 1,1,2-trimethylpropylcarbonyl, 1,2,2-trimethylpropylcarbonyl, l-ethyl-l-methylpropylcarbonyl or l-ethyl-2-methylpropylcarbonyl;

- C1-C4-alkylsulfenyl; methylsulfenyl, ethylsulfenyl, n-propylsulfenyl, l-methylethylsulfenyl, n-butylsulfenyl, l-methylpropylsulfenyl, 2-methylpropylsulfenyl, l,l-dimethyl-ethylsulfenyl, n-pentylsulfenyl, l-methylbutylsulfenyl, 2-methylbutylsulfenyl, 3-methylbutylsulfenyl, 2,2-dimethyl-propylsulfenyl, l-ethylpropylsulfenyl, l,l-dimethylpropyl-sulfenyl, 1,2-dimethylpropylsulfenyl, n-hexylsulfenyl, l-methylpentylsulfenyl, 2-methylpentylsulfenyl, 3-methyl-pentylsulfenyl, 4-methylpentylsulfenyl, l,l-dimethylbutyl-sulfenyl, 1,2-dimethylbutylsulfenyl, 1,3-dimethylbutyl-sulfenyl, 2,2-dimethylbutylsulfenyl, 2,3-dimethylbutyl-sulfenyl, 3,3-dimethylbutylsulfenyl, l-ethylbutylsulfenyl, 2-ethylbutylsulfenyl, 1,1,2-trimethylpropylsulfenyl, 1,2,2-trimethylpropylsulfenyl, l-ethyl-l-methylpropylsulfenyl or l-ethyl-2-methylpropylsulfenyl;

- Cl-C4-alkylsulfonyl: methylsulfonyl, ethylsulfonyl, n-propylsulfonyl, l-methylethylsulfonyl, n-butylsulfonyl, l-methylpropylsulfonyl, 2-methylpropylsulfonyl, l,l-dimethyl-ethylsulfonyl, n-pentylsulfonyl, l-methylbutylsulfonyl, 2-methylbutylsulfonyl, 3-methylbutylsulfonyl, 2,2-dimethyl-propylsulfonyl, l-ethylpropylsulfonyl, l,l-dimethylpropyl-sulfonyl, 1,2-dimethylpropylsulfonyl, n-hexylsulfonyl, l-methylpentylsulfonyl, 2-methylpentylsulfonyl, 3-methyl-pentylsulfonyl, 4-methylpentylsulfonyl, l,l-dimethylbutyl-sulfonyl, 1,2-dimethylbutylsulfonyl, 1,3-dimethylbutyl-sulfonyl, 2,2-dimethylbutylsulfonyl, 2,3-dimethylbutyl-sulfonyl, 3,3-dimethylbutylsulfonyl, l-ethylbutylsulfonyl, 2-ethylbutylsulfonyl, 1,1,2-trimethylpropylsulfonyl, 1,2,2-trimethylpropylsulfonyl, l-ethyl-1-methylpropylsulfonyl or 1-ethyl-2-methylpropylsulfonyl;

- Cl-C6-alkylideneaminoxy: acetylideneaminoxy, l-propylidene-aminoxy, 2-propylideneaminoxy, 1-butylideneaminoxy, 2-butylideneaminoxy or 2-hexylideneaminoxy;

- C3-C8-cycloalkyl: cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and cyclooctyl;
- C3-C8-cycloalkoxy: cyclopropyloxy, cyclobutyloxy, cyclopentyloxy, cyclohexyloxy, cycloheptyloxy and cyclooctyloxy.

15 Examples of 3- to 7 ;e ~red heterocycles are oxiranyl, aziridinyl, oxetanyl, tetrahydrofuranyl, tetrahydrothienyl, pyrrolidinyl, isoxazolidinyl, isothiazolidinyl, pyrazolidinyl, oxazolidinyl, thiazolidinyl, imidazolidinyl, dioxolanyl, such as 1,3-dioxolan-2-yl and 1,3-dioxolan-4-yl, l,3-dioxan-2-yl, 20 1,3-dioxan-4-yl, 1,3-dithian-2-yl, 1,2,4-oxadiazolidinyl, 1,3,4-oxadiazolidinyl, 1,2,4-thi A~; ~ zolidinyl, 1,3,4-thiadiazolidinyl, 1,2,4-t~iazolidinyl, 1,3,4-triazolidinyl, 2,3-dihydrofuryl, 2,5-dihydrofuryl, 2,3-dihydrothienyl, 2,5-dihydrothienyl, 2,3-pyrrolinyl, 2,5-pyrrolinyl, 25 2,3-isoxazolinyl, 3,4-isoxazolinyl, 4,5-isoxazolinyl, 2,3-isothiazolinyl, 3,4-isothiazolinyl, 4,5-isothiazolinyl, 2,3-dihydropyrazolyl, 3,4-dihydropyrazolyl, 4,5-dihydropyrazolyl, 2,3-dihydrooxazolyl, 3,4-dihydrooxazolyl, thiazolyl, imidazolyl, 1,2,4-oxadiazolyl, 1,3,4-oxadiazolyl, 1,2,4-thi~iazolyl, 30 1,3,4-thiadiazolyl, 1,2,4-triazolyl and 1,3,4-triazolyl, piperidinyl, tetrahydropyridazinyl, tetrahydropyrimidinyl, tetrahydropyrazinyl, 1,3,5-tetrahydrotriazinyl and 1,2,4-tetrahydrotriazinyl, and the following heteroaromatics:
2-furyl, 3-furyl, 2-thienyl, 3-thienyl, 2-pyrrolyl, 3-pyrrolyl, 3-isoxazolyl, 4-isoxazolyl, 5-isoxazolyl, 3-isothiazolyl, 4-isothiazolyl, 5-isothiazolyl, 1-pyrazolyl, 3-pyrazolyl, 4-pyrazolyl, 2-oxazolyl, 4-oxazolyl, 5-oxazolyl, 2-thiazolyl, 40 4-thiazolyl, 5-thiazolyl, l-imidazolyl, 2-imidazolyl, 4-imidazolyl, 1,2,4-oxadiazol-3-yl, 1,2,4-ox~ zol-5-yl, 1,2,4-thiadiazol-3-yl, 1,2,4-thi~iAzol-5-yl, 1,2,4-triazol-1-yl, 1,2,4-triazol-3-yl, 1,2,4-triazol-4-yl, 1,3,4-oxadiazol-2-yl, 1,3,4-thiadiazol-2-yl, 2-pyridinyl, 3-pyridinyl, 4-pyridinyl, 45 3-pyridazinyl, 4-pyridazinyl, 2-pyrimidinyl, 4-pyrimidinyl, 5-pyrimidinyl, 2-pyrazinyl, 1,3,5-triazin-2-yl and .
1,2,4-triazin-3-yl, in particular pyridyl, pyrimidyl, furanyl and thienyl.

All phenyl- and heterocyclic rings are preferably unsubstituted S or have attached to them a halogen, methyl, trifluoromethyl or methoxy qubstituent.

With a view to the use of the novel compounds of the formula I as herbicides and~or as compounds with a defoliant/desiccant action, 10 the variables preferably have the following meanings, in each case on their own or in combination:

A is amino or methyl;

15 Y is oxygen;

Rl is hydrogen, fluorine or chlorine, in particular hydrogen or fluorine;

20 R2 is Cl-C6-alkyl, Cl-C6-haloalkyl or Cl-C6-alkylsulfonyl, in particular Cl-C4-haloalkyl, particularly preferably trifluoromethyl, chlorodifluoromethyl or pentafluoroethyl;

R3 i9 hydrogen or halogen, in particular hydrogen, chlorine or bromine;

R4 is hydrogen, C1--C6--haloalkyl,Cl--C6--alkyl,C3--C8--cyclo-alkyl, C3-C6-alkenyl, C3-C6-alkynyl, (Cl-C6-alkyl)-carbonyl, (C3-C6-alkenyl)carbonyl or (C3-C6-alkynyl)-carbonyl, it being possible, if desired, for each of the last-mentioned 8 radicals to have attached to it one or two ~ubstituents, in each case selected from the group consisting of halogen, nitro, cyano, hydroxyl, C3-C8-cycloalkyl, C1--C6--alkoxy,C3--CB--cycloalkoxy, c3-c6-alkenyloxy~
C3-C6-alkynyloxy, Cl-C6-alkoxy-Cl-C6-alkoxy, Cl-C6-alkylthio, Cl-C6-alkylsulfenyl, Cl-C6-alkylsulfonyl, C1--C6--alkylideneaminoxy,--Co--XR5,~ Co--XR5or --N(R5)R6, in particular hydrogen, Cl-C4-alkyl, C3-C6-cycloalkyl, C3-C4--alkenyl, C3-C4--alkynyl, Cl-C4-haloalkyl, Cl-C4-alkoxy-C1-C4-alkyl, (C1-C4-alkyl)carbonyl, -CH2-Co-XR5, -CH(CH3 )-Co-XR5 or C1-C4-cyanoalkyl, such as cyanomethyl, l-cyanoeth-l-yl, 2-cyanoeth-1-yl, l-cyanoprop-1-yl, 2-cyanoprop-1-yl, 3-cyanoprop-1-yl, 1-cyanoprop-2-yl, 2-cyanoprop-2-yl, 1-cyanobut-1-yl, 2-cyanobut-1-yl, 3-cyanobut-1-yl, 4-cyanobut-1-yl, 1-cyanobut-2-yl, 2-cyanobut-2-yl, 1-cyanobut-3-yl, 2-cyanobut-3-yl, 1-cyano-2-methylprop-3-yl, 2-cyano-2-methylprop-3-yl, 3-cyano-2-methylprop-3-yl and 2-cyano-methylprop-2-yl;

5 X is a chemical bond, oxygen or -N(R6)-;

R5 is hydrogen, Cl-C6-alkyl, C3-C8-cycloalkyl, C3-C6-alkenyl, C3-C6-alkynyl, C1-C6-alkoxy-C1-C6-alkyl or (C1-C6-alkoxy)carbonyl-C1-C6-alkyl, in particular hydrogen, C1-C6-alkyl, C3-C8-cycloalkyl, C1-C6-alkoxy-C1-C6-alkyl or (C1-C6-alkoxy)carbonyl-C1-C6-alkyl, R6 is hydrogen, C1-C6-alkyl or C1-C6-alkoxy.

Very particularly preferred are the compounds Ia which are listed 15 in Table 1 below (~ I where A = amino, Y = oxygen, R1 = fluorine, R2 = trifluoromethyl, R3 = hydrogen):

H2~ ~ O F
N ~ CN Ia ~\ ~
H O oR4 25 Table 1 No. R4 Ia.01 H
Ia.02 CH3 30 Ia.03 C2H5 Ia.04 n-C3H7 Ia.05 CH(CH3)2 Ia.06 n-C4Hg Ia.07 i-C4Hg Ia.08 8-C4Hg Ia.09 C(CH3)3 Ia.10 cyclopropyl Ia.ll cyclobutyl Ia.12 cyclopentyl Ia.13 cyclohexyl Ia.14 cycloheptyl Ia.15 cyclooctyl 45 Ia.16 CH2CN
Ia.17 CH2CH2CN

'0050/45615 No. R4 Ia.18 CH(CH3)CN
Ia.l9 C(CH3)2CN
5 Ia.20 C(CH3)2CH2CN
Ia.2l CH2Cl Ia.22 CH2CH2Cl Ia.23 CH(CH3)CH2Cl Ia.24 CH2CF3 Ia.25 CHC12 Ia.26 CF2Cl Ia.27 CF3 Ia.28 C2Fs 15 Ia.29 CF2H
Ia.30 CH2-CH=CH2 Ia.31 CH~CH3)-CH=cH2 Ia.32 CH2-CH=CH-CH3 20 Ia.33 CH2-C-CH
Ia.34 CH(CH3)-C-CH
Ia.35 C(CH3)2-C-CH
Ia.36 CH2-COOH
25 Ia.37 CH2-CO-OCH3 Ia.38 CH2-CO-OC2H5 Ia.39 CH2-CO-O-n-C3H7 Ia.40 CH2-CO-OCH(CH3)2 Ia.41 CH(CH3)-CO-OCH3 30 Ia.42 CH(CH3)-CO-OC2H5 Ia.43 CH(CH3)-CO-O-n-C3H7 Ia.44 CH(CH3)-CO-OC(CH3)2 Ia.45 CH2-COO-(CH2)2-OCH3 35 Ia.46 CH2-COO-~CH2)2-OCH3 Ia.47 CH(CH3)-COO-(CH2)2-OCH3 Ia.48 cH(cH3)-coo-(cH2)2-oc2Hs Ia.49 CH2-CONH2 40 Ia.50 CH2-CONHCH3 Ia.51 CH2-CONHC2H5 Ia.52 CH2-CON(CH3)2 Ia.53 CH(CH3)-cONH2 Ia.54 CH(CH3)-CONHCH3 Ia.55 CH(CH3)-CONHC2H5 Ia.56 CH(CH3)-CON(CH3)2 0050/g5615 No. R4 Ia.57 CO-CH3 Ia.58 CO-C2H5 5 Ia.59 CO-CH(CH3)2 Ia.60 CO-n-C4Hg Ia.61 CO-cyclopropyl Ia.62 CO-cyclopentyl Ia.63 CO-CF3 Ia.64 CO-OCH3 Ia.65 CO-OC2H5 Ia.66 SO2-CH3 Ia.67 CH2-SCH3 15 Ia.68 (CH2)2-SCH3 Ia.69 (CH2)2-SC2H5 Ia.70 (CH2)2-SO-CH3 Ia.71 (CH2)2-SO2-CH3 20 Ia.72 (CH2)2-SO-CH3 Ia.73 (CH2)2-cyclopropyl Ia.74 (CH2)2-cyclopentyl Ia.75 (CH2)2-ONZc~cH3) 2 25 Ia.76 (CH2)3-ON=C(CH3)2 Ia.77 (CH2)2-NO2 Ia.78 (CH2)2-NH2 Ia.79 (CH2)2-NHCH3 Ia.80 (CH2)2-NH(CH3)2 30 Ia.81 CH2-OCH3 Ia.82 CH(CH3)-OCH3 Ia.83 CH(CH3)-OC2H5 Ia.84 CH(CH3)CH2-OCH3 35 Ia.85 (CH2)2OH

Ia.86 CH2-Oc2H5 Ia.87 CH2COO-(4-acetoxytetrahydrofuran-3-yl) Ia.88 CH2OCOCH3 40 Ia.89 CH2OCOC2H5 Ia.90 CH2C6Hs Ia.91 (CH2)2-C6H5 Ia.92 CH2-(4-Cl-C6H4) Ia.93 CH2-(4-CF3-C6H4) Ia.94 CH2-(3-NO2-C6H4) Other particularly preferred 3-(4-cyanophenyl)uracils of the formula I are those which follow:

- the compounds Ib.01 - Ib.94, which only differ from the corresponding compounds Ia.Ol - Ia.94 by the fact that Rl is hydrogen:

H2N\ ~ o H
F3C~N~ CN Ib H o oR4 15 - the compounds Ic.01 - Ic.94, which only differ from the corresponding compounds Ia.01 - Ia.94 by the fact that Rl is chlorine:

/~ CN Ic H O oR4 - the compounds Id.01 - Id.94, which only differ from the corresponding compounds Ia.01 - Ia.94 by the fact that A is methyl:

H3(~, O F
N~// \~
F3C~N ~_ \~ CN Id 3 5 H ~ oR4 - the compounds Ie.01 - Ie.94, which only differ from the corresponding compounds Ia.Ol - Ia.94 by the fact that A i8 hydrogen:

/ ~ CN I~3 H O oR4 - the compounds If.01 - If.94, which only differ from the corresponding compounds Ia.01 - Ia.94 by the fact that Rl is hydrogen and A is methyl:

H3C\N ~ H

F3C ~ N CN If H ~ oR4 - the compounds Ig.01 - Ig.94, which only differ from the corresponding compounds Ia.01 - Ia.94 by the fact that Rl and A are hydrogen:

F C ~ ~ N ~ CN Ig H o oR4 - the compounds Ih.01 - Ih.94, which only differ from the corresponding compounds Ia.01 - Ia.94 by the fact that R1 i8 chlorine and A is methyl:

~ \ ~ Ih B o oR4 - the compounds Ii.01 - Ii.94, which only differ from the corresponding compounds Ia.01 - Ia.94 by the fact that Rl is chlorine and A is hydrogen:
/o C\
~C ~ N ~ CN Ii H o oR4 - the compounds Ik.Ol - Ik.94, which only differ from the corresponding compounds Ia.Ol - Ia.94 by the fact that R3 is chlorine:

5H2N\ ~ o F

F3C~N~ CN Ik 10Cl o oR4 - the compounds Il.O1 - Il.94, which only differ from the corresponding compounds Ia.O1 - Ia.94 by the fact that R3 is chlorine and A is methyl:

H3C \ o F
N~
F3C~N~ CN I 1 Cl O oR4 - the compounds Im.O1 - Im.94, which only differ from the corresponding compounds Ia.Ol - Ia.94 by the fact that R3 is chlorine and A is hydrogen:

H~ ~ O F

N ~ CN Im c 1 o oR4 - the compounds In.O1 - In.94, which only differ from the corresponding compounds Ia.Ol - Ia.94 by the fact that R1 and R3 are chlorine:

H2N~ ~ O Cl 40F3C ~ N ~ \~ CN In c 1 o oR4 - the compounds Io.Ol - Io.94, which only differ from the corresponding compounds Ia.O1 - Ia.94 by the fact that A is methyl, Rl is hydrogen and R3 is chlorine:

H3C\ o H

F3C ~ N - ~ CN Io Cl ~ oR4 - the compounds Ip.Ol - Ip.94, which only differ from the corresponding compounds Ia.Ol - Ia.94 by the fact that A is methyl and Rl and R3 are chlorine;

H3C ~ O Cl F3C ~ N ~ CN Ip c 1 o oR4 The 3-(4-cyanophenyl)uracils of the formula I can be obt~i neA by various routes, for example by one of the following processes:
Process A):
Cyclization of an enA ine ester of the formula III or of an enA 1ne carboxylate of the formula IV in the presence of a base:

O ~ .
\ ~ - NH ~ CN
R2 _ ~ ~ OLl \ \

R3 o III ~ base I (Y=O) \N ~ - OLl Rl /
R2_ ~ NH ~ CN

R3 IV oR4 Ll is low-molecular-weight alkyl, preferably Cl-C4-alkyl, or phenyl.

As a rule, the cyclization is carried out in an inert organic 5 solvent or diluent which is aprotic, for example in an aliphatic or cyclic ether, such as 1,2-dimethoxyethane, tetrahydrofuran and dioxane, in an aromatic, such as benzene and toluene, or in a polar solvent, such as dimethylformamide and dimethyl sulfoxide.
Mixtures of polar solvents and a hydrocarbon, such as n-hexane, 10 are also suitable. Depending on the starting material, water may also be suitable as the diluent.

Suitable bases are, preferably, alkali metal alcoholates, in particular the sodium alcoholates, alkali metal hydroxides, in 15 particular sodium hydroxide and potassium hydroxide, alkali metal carbonates, in particular sodium carbonate and potassium carbonate, and metal hydrides, in particular sodium hydride. If sodium hydride is used as the base, it has proved advantageous to carry out the process in an aliphatic or cyclic ether, in 20 dimethylformamide or in dimethyl sulfoxide.

0.5 times to twice the molar amount of base based on the amount of III or IV is generally sufficient to carry out the reaction successfully.
In general, the reaction temperature is from ~-78) C to the boiling point of the reaction mixture in question, in particular from (-60) to 60~C.

30 If A in formula III or IV is hydrogen, the process product is obtained as a metal salt, the metal corresponding to the cation of the base used. The salt can be isolated and purified in a manner known per se or, if desired, converted using an acid to obtain the free compound I where A = hydrogen.

Process B):
Methylation of a compound I where A is hydrogen in the presence of a base:

CN ~C~33~3~ ~ ~2 ~ CN

R3 Y oR4 R3 Y OR4 I (A=H) I (A=CH3) Examples of suitable methylating agents are methyl halides, preferably methyl chloride, methyl iodide or methyl bromide, and also dimethyl sulfate, methyl methanesulfonate (methyl mesylate), methyl benzenesulfonate, methyl p-toluenesulfonate (methyl 20 tosylate), methyl p-bromobenzenesulfonate (methyl brosylate), methyl trifluoromethanesulfonate (methyl triflate) and diazomethane.

As a rule, the process is carried out in an inert organic solvent 25 or in an aprotic solvent, eg. in an aliphatic or cyclic ether, preferably in 1,2-dimethoxyethane, tetrahydrofuran or dioxane, in an aliphatic ketone, preferably in acetone, in an amide, preferably in dimethylformamide, in a sulfoxide, preferably in dimethyl sulfoxide, in a urea, such as tetramethylurea and 30 1,3-dimethyltetrahydro-2(lH)-pyrimidinone, in a carboxylic ester, such as ethyl acetate, or in a halogenated aliphatic or aromatic hydrocarbon, such as dichloromethane and chlorobenzene.

Suitable bases are inorganic bases, eg. carbonates, such as 35 sodium carbonate and potassium carbonate, hydrogen carbonates, such as sodium hydrogen carbonate or potassium hydrogen carbonate, or alkali metal hydrides, such as sodium hydride and potassium hydride, and also organic bases, eg. amines, such as triethylamine, pyridine and N,N-diethylaniline, or alkali metal 40 alcoholates, such as sodium methanolate, sodium ethanolate and potassium tert-butanolate.

The amount of base and methylating agent is preferably 0.5 times to twice the molar amount based on the amount of starting 45 compound.

In general, the reaction temperature is from 0 C to the boiling point of the reaction mixture, in particular from 0 to 60~C.

A preferred process variant consists in methylating the salt of 5 I, which has been obtained by cyclizing III (A = H) or IV (A = H) in accordance with process A) without isolating it from the reaction mixture, which can still contain excess base, eg. sodium hydride, sodium alcoholate or ~odium carbonate.

10 If the salts of those compounds I where A is hydrogen cannot be prepared directly by the cyclization under alkaline conditions, which has been described as method a), they can also be obtained from the process products obtained by method a) in a manner known per se. For this purpose, for example, the aqueous solution of an 15 inorganic or organic base is treated with the substituted 3-(4-cyanophenyl)uracil I where A is hydrogen. Salt formation usually takes place at sufficiently high rates at as little as 20-25~C.

20 It i8 particularly advantageous to prepare the sodium salt by dissolving the 3-(4-cyanophenyl)uracil I (A = hydrogen) in aqueou~ sodium hydroxide solution at 20-25 C, using approximately equivalent amounts of 3-~4-cyanophenyl)uracil and sodium hydroxide. The salt of the 3-(4-cyanophenyl)uracil can then be 25 isolated for example by precipitation with a suitable inert solvent or by evaporating the solvent.

Salts of the 3-(4-cyanophenyl)Yracils whose metal ion is not an alkali metal ion can generally be prepared by double 30 decomposition of the corresponding alkali metal salt in aqueous solution. 3-(4-cyanophenyl)uracil metal salts which are insoluble in water can be prepared in this manner, for example.

Process C):
Reaction of a 3-(4-cyanophenyl)uracil of the formula I where A iB
hydrogen with an electrophilic aminating reagent in the presence of a base;
s base / ~ CN

R3 Y oR4 R3Y oR4 I (A=H) I (A=NH2) An aminating reagent which has proved useful to date is 2,4-dinitrophenoxyamine, but hydroxylamine-O-sulfonic acid (HOSA), which has been disclosed in the literature as aminating 20 reagent, can, for example, also be used (cf., for example, E. Hofer et al., Synthesis 1983, 466; W. Friedrichsen et al., Heterocycles 20 (1983) 1271; H. Hart et al., Tetrahedron Lett.
(1984) 2073; ~. Vercek et al., Monatsh. Chem. 114 (1983) 789; G.
Sosnousky et al., Z. Naturforsch. 38 (1983) 884; R.S. Atki~on et 25 al., J. Chem. Soc. Perkin Trans. 1987, 2787).

Amination can be carried out in a manner known per se (see, for example, T. Sheradsky, Tetrahedron Lett. 1948, 1909;
M.P. Wentland et al., J. Med. Chem. 27 (1984) 1103, and, in 30 particular, EP-A 240 194, EP-A 476 697 and EP-A 517 181, which teach the amination of uracils).

The reaction is usually carried out in a polar solvent, eg. in dimethylformamide, N-methylpyrrolidone, dimethyl sulfoxide or in 35 ethyl acetate, which has proved particularly useful to date.

Examples of suitable bases are alkali metal carbonates, such as potassium carbonate, alkali metal alcoholate~, ~uch as sodium methylate and potassium tert-butanolate, or alkali metal 40 hydrides, such as sodium hydride.

The amount of base and aminating agent is preferably in each case 0.5 times to twice the molar amount based on the amount of starting compound.

~ .

Depending on the meaning of R4, it may be necessary to protect this substituent in a manner known per se prior to amination.
This is particularly to be recor ?n~ed if R4 is hydrogen.

5 Process D):
Sulfuration of a 3-~4-cyanophenyl)uracil of the formula I where Y = oxygen:

A o Rl A o R1 N / ~ CN Sulfuration ~ R2 ~ N ~ CN

R3 ~ oR4 R3 S oR4 I (Y=O) I (Y=S) The sulfuration is qenerally csrried out in an inert solvent or diluent, for example in an aromatic hydrocarbon, such as toluene and the xylenes, in an ether, such as diethyl ether, 1,2-dimethoxyethane and tetrahydrofuran, or in an organic amine, 20 such as pyridine.

Particularly suitable sulfurating reagents are phosphorus(V) sulfide and 2,4-bis(4-methoxyphenyl)-1,3,2,4-dithiadiphosphetane-2,4-dithione ("Lawesson's reagent").
1 to 5 times the molar amount based on the starting compound to be sulfurized is generally sufficient for an essentially complete reaction.

30 The reaction temperature usually is from 20 to 200 C, preferably 40 C to the boiling point of the reaction mixture.

Process E):
Ether cleavage of a 3-(4-cyanophenyl)uracil of the formula I
35 where R4 is an unsubstituted or substituted alkyl, cycloalkyl, alkenyl, alkynyl or benzyl:

A o R1 A o Rl R2 ~ N ~ \~ CN ~ RZ ~ N ~ CN

R3 Y OR4 R3 y OH
~R4 = unsubstituted or I (R4=H) substituted alkyl, cycloalkyl, alkenyl, alkynyl) The ether cleava~e is usually effected by means of an acid, eg.
by means of hydrogen bromide, hydrogen iodide or pyridinium hydrochloride, by means of a Lewis acid, such as aluminum trichloride, aluminum tribromide, aluminum triiodide, boron 5 trichloride, boron tribromide, boron trifluoride and iron trichloride, or by mean~ of trimethylsilyl iodide. Other useful substances for cleaving the ether bond are, however, also lithium salts, such a~ lithium chloride, or mixtures of an inorganic iodide and trimethylsilyl chloride. In individual cases, for 10 example when R4 is benzyl, the bond can also be cleaved under hydrogenation conditions using hydrogen in the presence of a hydrogenation cataly~t, such as platinum and palladium on active charcoal.

15 Allyl ether~ (R4 = allyl) can furthermore be converted into the corresponding phenols in a manner known per se for this purpose, for example by isomerization in the presence of a transition metal catalyst to give the enol ether and cleavage of the latter, preferably under mildly acidic conditions (cf., for example, 20 T. Greene and P.G.M. Wutz in nProtective Groups in Organic Synthesis", John Wiley & Sons, 2nd Edition, New York 1991, p. 42 et seq.).

The process is generally carried out in an inert solvent or 25 diluent, eg. in an aliphatic, cyclic or aromatic hydrocarbon, such as n-pentane, petroleum ether, cycloheYAne, benzene, toluene or xylene, an aliphatic or cyclic ether, such as diethyl ether, tert-butyl methyl ether, dimethoxyethane and tetrahydrofuran, an aliphatic or aromatic halogenated hydrocarbon, such as 30 dichloromethane, chloroform, chlorobenzene, 1,2-dichloroethane and the dichlorobenzenes, an alcohol, such as methanol, ethanol and tert-butanol, an amide, such as dimethylformamide and N-methylpyrrolidone, an amine, such as ammonia, or in a mixture of these.
It may also be advantageous to carry out the reaction in the absence of a solvent.

With regard to particularly preferred embodiments, mention may be 40 made of the information given in Houben-Weyl, "Methoden der Organischen Chemie" [Methods in Organic Chemistry], Georg Thieme Verlag, 4th Edition, Stuttgart 1979, Vol. 6/la/1, p. 309 et seq., and in R. C. Larock, "Comprehensive Organic Transformations", VCH-Publishers, Weinheim 1989, p. 501 et seq., and the literature 45 cited in these publications.

'' 0050/45615 Process F):
Alkylation of a 3-(4-cyanophenyl)uracil of the formula I where R4 is hydrogen in the presence of a base:

~se ~ CN

R3 y OH R3 Y oR4 I (R4=H) I(R4=~ s~ lt~dors~hs~it~ltçdalkyl, cycloalkyl, alkenyl or alkynyl) The alkylation can be carried out, for example, using the halide, preferably the chloride or bromide, the sulfate, sulfonate, preferably the methanesulfonate (mesylate), benzenesulfonate, p-toluenesulfonate (tosylate), p-bromobenzenesulfonate 20 (brosylate), the trifluoromethanesulfonate (triflate) or the diazo compound of an unsubstituted or substituted alkane, cycloAlk~ne, haloalkane, alkene or alkyne.

The reaction is usually carried out in an inert organic solvent, 25 suitable solvents being, in particular, aprotic solvents, eg.
aliphatic and cyclic ethers, such as 1,2-dimethoxyethane, tetrahydrofuran and dioxane, aliphatic ketones, such as acetone, amides, such as dimethylformamide, sulfoxides, such as dimethyl sulfoxide, ureas, such as tetramethylurea and 30 1,3-dimethyltetrahydro-2(lH)-pyrimidinone, carboxylic esters, such as ethyl acetate, or halogenated aliphatic or aromatic hydrocarbons, such as dichloromethane and chlorobenzene.

Suitable bases are inorganic bases, eg. alkali metal carbonates, 35 such as sodium carbonate and potassium carbonate, alkali metal hydrogencarbonates, such as sodium hydrogen carbonate and potassium hydrogen carbonate, or alkali metal hydrides, such as sodium hydride and potassium hydride, but also organic bases, eg.
amines, such as triethylamine, pyridine and N,N-diethylaniline, 40 or alkali metal alcoholates, such as sodium methanolate, sodium ethanolate and potassium tert-butanolate.

The amount of base and alkylating agent is preferably 0.5 times to twice the molar amount based on the amount of I where 45 R4 = hydrogen.

In general, a reaction temperature of from 0 C to the boiling point of the reaction mixture, in particular from 0 to 60 C, is recommended.

5 Any problems with regioselectivity in the case of starting compounds where A = hydrogen can be avoided in a manner known per se (use of 2 equivalents of base, introduction of a protective group etc.).

10 Process G):
Acylation of a 3-(4-cyanophenyl)uracil of the formula I where R4 is hydrogen with a suitable alkylating agent.

Z = ~ ~ CN

R3 y OH R3 Y oR4 I (R4=H) I(R4=s~hs~h-~Pdor~
alkyl--, alkenyl--or alkynylcarbonyl) 25 Suitable acylating agents are for example the acid halides, in particular the acid chlorides, the anhydrides, isocyanates or sulfonylchlorides of alkane-, cycloalkane-, alkene-, alkyne-, phenyl- or phenylalkanecarboxylic acids. However, the free acids or their anhydrides are also suitable, under the condition that 30 the process is carried out in the presence of a co~ensing agent, such as carbonyl diimidazole and dicyclohexylcarbodiimide.

The process is generally carried out in an inert organic solvent or diluent which is preferably aprotic, eg. in an aliphatic or 35 cyclic ether, such as 1,2-dimethoxyethane, tetrahydrofuran and dioxane, an aliphatic ketone, such as acetone, an amide, such as dimethylformamide, a urea, such as tetramethylurea and 1,3-dimethyltetrahydro-2(lH)-pyrimidinone, a carboxylic ester, such as ethyl acetate, or an aliphatic or aromatic halogenated 40 hydrocarbon, such as dichloromethane and chlorobenzene.

As regards suitable bases, the weight ratios and the reaction temperature, the information given for process F) applies.

45 Process H):
Substitution of halide by cyanide:

'' 0050/45615 Process H):
Substitution of halide by cyanide:

Cll R3 Y oR4 R3 Y oR4 V

Hal is halogen, preferably fluorine, bromine or iodine.
Suitable cyanides are, in particular, metal cyanides, eg. the alkali metal cyanides, such as lithium cyanide, sodium cyanide and potassium cyanide, the alkaline earth metal cyanides, such as magnesum cyanide, or else transition metal cyanides, such as 20 copper cyanide.

The process is usually carried out in an ether, such as tetrahydrofuran, dioxane and 1,2-dimethoxyethane, or in an aprotic polar solvent, eg. an alkyl nitrile, 4uch as 25 acetonitrile, propionitrile and butyronitrile, an alkylurea, such as N,N,N',N'-tetramethylurea, an open-chain or cyclic dialkylamide, such as dimethylformamide, N-methyl-2-pyrrolidone, 1,2-dimethylimidazolidin-2-one and 1,2-dimethyl-3,4,5,6-tetrahydro-2(lH)-pyrimidinone, a dialkyl 30 sulfoxide, such as dimethyl sulfoxide, or in hexamethylphosphoric triamide.

Findings to date have revealed that the presence of a catalyst may have an advantageous effect on the course of the reaction.
35 Examples of suitable catalysts are transition metals and their complexes or salts, eg. copper compounds, such as copper(I) chloride, copper(I) iodide, copper(I) cyanide, or nickel compounds, such as nickel bis-triphenylphosphine dibromide.

40 In the case of starting compounds V where A = hydrogen, it is recommended to carry out the process in the presence of a base, suitable bases being, in particular, weakly nucleophilic bases, ie. inorganic bases, eg. alkali metal carbonates, such as sodium carbonate and potassium carbonate, alkali metal hydrogen 45 carbonates, such as sodium hydrogen carbonate and potassium hydrogen carbonate, or alkali metal hydrides, such as sodium hydride and potassium hydride, and also organic bases, eg.
amines, such as triethylamine, pyridine and N,N-diethylaniline.

The weight ratios are usually not critical. In general, 5 approximately one to 10 times the amount of cyanide and base, based on the amount of V, will suffice.
The reaction temperature is usually 50 to 250 C; however, to increase the selectivity of the reaction, it may also be 10 advantageous to carry out the process at lower temperatures, in particular at approximately 20~C.

~ith regard to various embodiments of this reaction, reference may be made to Houben-Weyl, "Methoden der Organischen Chemie"
15 lMethods in Organic Chemistry], Georg Thieme Verlag, 4th Edition, Stuttgart 1985, Vol. E5, p. 1444 et se~., and the literature cited therein.

Process I):
20 ~alogenation of a 3-(4-cyanophenyl)uracil of the formula I where R3 is hydrogen N ~ o R1 ~ Y 0~ R3 Y OR4 I (R3=H) I (R3=halogen) The halogenation is generally carried out in an inert organic solvent or diluent. Suitable substances for the chlorination and 35 bromination are, for example, aliphatic carboxylic acids, such as acetic acid, or chlorinated aliphatic hydrocarbons, such as methylene chloride, chloroform and carbon tetrachloride.
Low-boiling aliphatic carboxylic acids, such as acetic acid, are particularly preferred for the iodination.
Particularly suitable for the chlorination and bromination are elemental chlorine or bromine, or sulfuryl chloride and sulfuryl bromide, respectively, at from preferably O to 60 C, in particular 10 to 30 C.

CA 022l0909 l997-07-30 If desired, the chlorination and bromination can be carried out in the presence of an acid binder, in which case sodium acetate and tertiary amines, such as triethylamine, dimethylaniline and pyridine, are particularly preferred.
A particularly preferred iodinating agent is elemental iodine, the reaction temperature in this case being from approximately 0 to 110 C, preferably from 10 to 30 C.

lO Particularly advantageous is the iodination in the presence of a mineral acid, such as fuming nitric acid.

The amount of halogenating agent is not critical; equimolar amounts of halogenating agent or an excess of up to 200 mol%
15 based on the precursor to be halogenated are generally used.

Excess iodine can be removed for example after the reaction by means of saturated aqueous sodium hydrogen sulfite solution.

20 Process K):
Substitution of the nitro group of 3-(4-cyano-3-nitrophenyl)uracils VI by a group -oR4:

~ \ ~ CN

R3 Y NO2 R3 Y oR4 VI

35 The substitution of the nitro group iB generally carried out by reacting VI with an alcoholate MoR4 where M i~ 8 metal atom, preferably lithium, sodium or potassium (cf., for example, Org.Synth. Coll. Vol. III, 293).

~O As a rule, the process is either carried out in the alcohol HoR4 whose alcoholate is used, or in an inert organic solvent or - diluent, eg. in an aromatic hydrocarbon, such as toluene and the xylenes, in an ether, such as diethyl ether, tetrahydrofuran and 1,2-dimethoxyethane, or in a halogenated hydrocarbon, such as 45 dichloromethane and chlorobenzene.

The reaction temperature is generally at from 0 to 150 C, preferably from room temperature (approximately 20 C) to the boiling point of the reaction mixture in question.

5 The amount of alcoholate is generally not critical; approximately 1 to 3 equivalents of alcoholate per mole of VI are preferred.

The 3-(4-cyano-3-nitrophenyl)uracils V, in turn, can be obtained for example from 3-(4-halo-3-nitrophenyl)uracils VII

A o Rl R2 ~ N ~ ~ halogen VII

by substituting the halogen by cyano. The information given for process H) apply analogously.
The 3-(4-halo-3-nitrophenyl)uracils VII, in turn, can be prepared for example by nitrating 3-(4-halophenyl)uracils VIII

A o Rl N ~/ ~
R2 ~ N ~ halogen VIII

using nitric acid, nitrating acid, an inorganic nitrate, such as sodium nitrate, potassium nitrate and ammonium nitrate, or an organic nitrate, such as amyl nitrate.

35 Suitable solvents for the nitration are, preferably, inorganic acids, such as nitric acid and sulfuric acid, organic acids, such as acetic acid, or anhydrides, such as acetic anhydride.

The reaction temperature is usually at from (-20) to 50 C, 40 preferably from (-10) to 30~C.

The amount of nitrating agent i8 not critical; it is usually one to 10 times the molar amount based on the amount of VI.

~ ' Process L):
Conversion of 3-(4-aminophenyl)uracils IX into compounds I by the Sandmeyer method:

A o R1 ~ ~ NH2 1 ) d azotization~ I

R3 Y oR4 IX
In this type of reaction, a procedure is generally followed in which the amino group is converted into the diazonium salt in a manner known per se, and this diazonium salt is subsequently 15 reacted with a metal cyanide, preferably lithum cyanide, sodium cyanide or potassium cyanide, in the presence of a transition metal catalyst, in particular copper(I) salt, expediently copper(I) cyanide.

20 As regards the process conditions, reference may be made, for example, to the information given in C. Ferri, ~'Reaktionen der organischen Chemie" [Reactions in Organic Chemistryl, Georg Thieme Verlag, Stuttgart 1978, p. 319, and in Organic Synthesis Coll. Vol 1, p. 514 (1941).
The starting compounds IX can preferably be prepared by reducing the corresponding nitro compounds using hydrogen in the presence of a metal catalyst composed of Raney nickel, palladium or platinum, or using a reducing agent, eg. a tin(II) salt or iron.
30 Further information on this reaction, which is known per se, can be found, for example, in DE-A 37 24 399.

The nitrated precursors corresponding to the compounds IX, in turn, can expediently be obtained by nitrating phenyl compounds X

A\ ~ o R

R2~<N ~ X

R3 Y oR4 The information given for the nitration of the 3-(4-halophenyl)uracils VII in process K) applies analogously to 45 the nitration of the phenyluracils X.

CA 022l0909 l997-07-30 Process M):
Direct cyanation of a phenyl compound X:

cyanation X ~ I
The cyanation can be carried out in the absence of a solvent or in an inert solvent or diluent, for example in an aliphatic, cyclic or aromatic hydrocarbon, such as n-pentane, petroleum lO ether and cyclohexane, an aliphatic or cyclic ether, such as diethyl ether, tert-butyl methyl ether, dimethoxyethane and tetrahydrofuran, an aliphatic or aromatic halohydrocarbon, such as dichloromethane, chloroform, 1,2-dichloroethane and the dichlorobenzenes, an alcohol, ~uch as ethanol, methanol and 15 tert-butanol, an amide, such as dimethylformamide and n-methylpyrrolidone, or an amine, such as ammonia. Mixtures of these are also suitable.

Suitable cyanide sources are alkyl thiocyanates, such as methyl 20 thiocyanate {cf., for example, Synth. C~ n. 20~ 71 (1990)}~
chlorosulfonyl isocyanate (cf., for example, Org. Synth. Coll.
Vol VI, p. 465), dicyan, chlorine cyanide and bromine cyanide, and furthermore trichloroacetonitrile {cf., in this context, Gazz. Chim. Ital. 122, 283 (1992)}.
The temperatures are usually at from (-20) to 150 C, preferably at from ~-10)~C to the boiling point of the reaction mixture in question.

30 The ratio of cyanating agent to IX is not critical; it is usually at from 1:1 to 10:1.

Modifications of this reaction are described, inter alia, in Houben-Weyl, "Methoden der Organischen Chemie" lMethods in 35 Organic Chemistryl, Georg Thieme Verlag, Vol. E5, 4th Edition, Stuttgart 1985, p. 1447 et seq. and in the literature cited therein.

Those starting compounds of the formulae VI, VII, VIII and IX
40 which are not known already can be prepared in a snner known per se ~cf., for example, EP-A 255 047, EP-A 517 181 and JP-A 05/025 143).

The enamine esters of the formula III are novel. They can also be 45 employed as herbicides.

They can be prepared by methods known per se, for example by one of the following processes:

N) R
~ A O Rl O
~ / N~ ~ \ ~--NH~ CN
H / \=~ R2--~\ OLl R3 O oR4 ) \~ oR4 15 The process is preferably carried out under essentially anhydrous conditions in an inert solvent or diluent, particularly preferably in the presence of an acidic or basic catalyst.

Suitable solvents or diluents are, in particular, organic 20 solvents which can be mixed with water to give an azeotropic mixture, for example aromatics, such as benzene, toluene and o-, m- and p-xylene, halogenated hydrocarbons, such as methylene chloride, chloroform, carbon tetrachloride and chlorobenzene, aliphatic and cyclic ethers, such as 1,2-dimethoxyethane, 25 tetrahydrofuran and dioxane, or cyclohexane, but also alcohols, such as methanol and ethanol.

Preferred suitable acidic catalysts are strong mineral acids, such as sulfuric acid and hydrochloric acid, 30 phosphorus-containing acids, such as orthophosphoric acid and polyphosphoric acid, organic acids, such as p-toluenesulfonic acid, and acidic cation exchangers, such as "Amberlyst 15"
(Fluka).

35 Examples of suitable basic catalysts are metal hydrides, such as sodium hydride, and, particularly preferably, metal alcoholates, such as sodium methanolate and sodium ethanolate.

XI and the ~-ketoester XII are expediently employed in an 40 approximately stoichiometric ratio, or else the process is carried out with a slight excess of one or the other component, up to approximately 10 mol%.

An amount of catalyst of 0.5 to 2 mol% based on the amount of 45 precursor will usually suffice.

~ 0050/45615 CA 02210909 1997-07-30 ~ ' In general, the reaction is carried out at from 60 to 120 C or, to rapidly remove water which forms, preferably up to the.boiling point of the reaction mixture.

5 0):

oL2 A o Rl R ~ OLl + N ~ ~ CN III
oR4 XIII XII

L2 is C1-C4-alkyl or phenyl.

This reaction can be carried out, for example, in an inert 20 organic solvent which is miscible with water, for example an aliphatic or cyclic ether, such as 1,2-dimethoxyethane, tetrahydrofuran and dioxane, or a lower alcohol, in particular ethanol, the reaction t~l,erature usually being at from 50 to 100 C, preferably at the boiling point of the reaction mixture.
However, the reaction can also be carried out in an aromatic diluent, such as benzene, toluene and o-, m- or p-xylene, in which case an addition of either an acidic catalyst, such as hydrochloric acid and p-toluenesulfonic acid, or of a base, eg.
30 an alkali metal alcoholate, such as sodium methanolate and sodium ethanolate, is recommended. In this process variant, the reaction temperature is usually again at from 50 to 100 C, but preferably at from 60 to 80~C.

35 With regard to the weight ratios, the information given for method N) applies.

P):

A~ Rl NH ~--R2 ~ OLl + OCN CN ~ III

R3 O oR4 XIV XV

The reaction i8 expediently carried out in the presence of an e6sentially anhydrous aprot$c organic solvent or diluent, for 15 example an aliphatic or cyclic ether, such as diethyl ether, 1,2-dimethoxyethane, tetrahydrofuran and dioxane, an aliphatic or aromatic hydrocarbon, such as n-hexane, ben2ene, toluene and o-, m- or p-xylene, a balogenated, aliphatic hydrocarbon, such a~
methylene chloride, chloroform, carbon tetrachloride, 20 1,2-dichloroethane and chlorobenzene, an aprotic, polar solvent, such as dimethylfo. ~id~, hexamethylphosphoric triamide and dimethyl sulfoxide, or a mixtures of these.

If desired, the process can also be carried out in the presence 25 of a metal hydride base, such as sodium hydride and potassium hydride, or an organic tertiary base, such as triethylamine and pyridine, it being possible for the organic base to act simultaneously as the solvent.

30 It is expedient to employ the precursors in a stoichiometric ratio or with a slight excess of one or the other components of up to approximately 10 mol%. If the process is carried out in the absence of a solvent and in the presence of an organic base, the latter will be present in a larger excess.
The reaction temperature is preferably at from ~-80) to 50 C, in particular at from (-60) to 30~C.

In a particularly preferred embodiment, the enamine ester III
40 obtained is converted directly (ie. "in situ") into the corresponding desired product I in accordance with process A), using an excess of base.

Q ) :

A~ ~ R
N H L30 ~/ \~
R2 ~oLl + N~ CN ~ III
oR4 XIV XVI
L3 is Cl-C4-alkyl or phenyl.

This reaction is expediently carried out in an aprotic, polar 15 solvent or diluent, such as dimethylformamide, 2-butanone, dimethyl sulfoxide and acetonitrile, advantageously in the presence of a base, for example an alkali metal alcoholate or alkaline earth metal alcoholate, in particular a sodium alkanolate, such as sodium methanolate, an alkali metal carbonate 20 or alkaline earth metal carbonate, in particular sodium carbonate, or an alkali metal hydride, such as lithium hydride and sodium hydride.

Once to twice the molar amount of base, based on the amount of 25 XIV or XVI, will usually suffice.

The reaction temperature is generally at from 80 to 180 C, preferably at the boiling point of the reaction mixture.

30 As regards the weight ratios of the starting compounds, the information given for method N) applies.

In a particularly preferred embodiment, a sodium alcoholate is used as the base, and the alcohol which forms in the course of 35 the reaction is continuously distilled off. The enamine esters III prepared in this manner can be cyclized without isolation from the reaction mixture in accordance with process A) to give a salt of the ~ubstituted 3-(4-cyanophenyl)uracil~ I.

R) NC0 ~
R2 ~ OLl + H2N ~ CN ~ ~ III

R3 0 oR4 XVII XVIII

This reaction is expediently carried out in the presence of an essentially anhydrous aprotic organic solvent or diluent, for 15 example an aliphatic or cyclic ether, such as diethyl ether, 1,2-dimethoxyethane, tetrahydrofuran and dioxane, an aliphatic or aromatic hydrocarbon, such as n-hexane, benzene, toluene and o-, m- or p-xylene, a halogenated, aliphatic hydrocarbon, such as methylene chloride, chloroform, carbon tetrachloride, 20 1,2-dichloroethane and chlorobenzene, an aprotic, polar solvent, such as dimethylformamide, hexamethylphosphoric triamide and dimethyl sulfoxide, or a mixtures of these.

If desired, the process can also be carried out in the presence 25 of a metal hydride base, such as sodium hydride and pota~sium hydride, an alkali metal alcoholate or alkaline earth metal alcoholate, such as sodium methanolate, ~odium ethanolate and potassium tert-butanolate, or an organic nitrogen base, such as triethylamine and pyridine, it being po~sible for the organic 30 base to act simultaneously as the solvent.

It is expedient to employ the precursors in a stoichiometric ratio or with an excess of one of the components of up to approximately 20 mol%. If the process is carried out in the 35 absence of a solvent and in the presence of an organic base, the latter is advantageously present in an even larger excess.

The reaction temperature i~ generally at from (-80) to 150 C, preferably at from (-30) C to the boiling point of the reaction 40 mixture in question.

The enA ine carboxylates of the formula IV are also novel; they too can be prepared in a manner known per se, for example from an aniline derivative of the formula VIII by the following equation:

'' 0050/45615 ~ ' (Eq. 1) o Rl Rl of C~3 ~ R4 ~ i XIX XVIII XX

~Eq. 2) O Rl A
R2 ~ OLl ~ Hl-COOLl (XXI) ~ ~ CN ~ XX ~ IV
oR4 XXI XVIII

The reaction in accordance with equation 1 i8 preferably carried 25 out in an anhydrous inert aprotic solvent, for example in a halogenated hydrocarbon, such a~ methylene chloride, chloroform, carbon tetrachloride and chlorobenzene, an aromatic hydrocarbon, such as benzene, toluene and o-, m- or p-xylene, or an aliphatic or cyclic ether, such as diethyl ether, dibutyl ether, 30 1,2-dimethoxyethane, tetrahydrofuran and dioxane.

For the reaction of XIX with XVIII in accordance with equation (Eq. 1), the reaction temperature is generally at from approximately 70 to 140~C, in particular from 100 to 120~C.
The reaction in accordance with equation (Eq. 2) is an aminolysis, which iB generally carried out either in the absence of a solvent [cf., for example, J. Soc. Dyes Col. 42, (1926), 81, Ber. 64, (1931), 970; Org. Synth., Coll. Vol. IV, (1943), 80 and 40 J.A.C.S. 70, (1948), 2402] or in an inert anhydrous solvent/diluent, in particular an aprotic solvent, for example in an aromatic, such as toluene and o-, m- or p-xylene, or a halogenated aromatic, such as chlorobenzene.

'' 0050/45615 ~ .

It is recommended to carry out the process in the presence of a basic catalyst, for example a higher-boiling amine [see, for example, Helv. Chim. Acta 11, (1928), 779 and U.S. 2,416,738] or pyridine.

The reaction temperature is preferably at from approximately 130 to 160 C.

In both reactions {(Eq. 1) and (Eq. 2)}, the starting compounds 10 are expediently employed in approximately stoichiometric amounts, or else the process is carried out with a slight excess of one or the other component of up to approximately 10 mol%. If the process is carried out in the presence of a basic catalyst, an amount of 0.5 to 2 mol% of catalyst based on the amount of one of 15 the educts will usually suffice.

The subsequent reaction of the resulting compounds of the formula XX with the amine XXI i8 advantageously carried out in an es~entially anhydrous solvent~diluent under atmospheric pressure, 20 particularly preferably in the presence of an acidic catalyst.

It is advisable to prepare enamine carboxylates IV where A is amino by employing compounds XXI having a protected amino group (for example in the form of a hydrazone).
Suitable solvents/diluents are, in particular, organic liquids which can be mixed with water to given an azeotropic mixture, for example aromatics, such as benzene, toluene and o-, m- or p-xylene, or halogenated hydrocarbons, such as carbon 30 tetrachloride and chlorobenzene.

Suitable catalysts are, in particular, strong mineral acids, such as sulfuric acid, organic acids, such as p-toluenesulfonic acid, phosphorus-cont~ n ~ ng acids, such as orthophosphoric acid and 35 polyphosphoric acid, or acidic cation exchangers, such as "Amberlyst 15" (Fluka).

The reaction temperature is generally at from approximately 70 to 150 C; however, to rapidly remove the water of reaction which 40 forms it is expedient to carry out the process at the boiling point of the reaction mixture in question.

Unless otherwise specified, all processes described above are expediently carried out under atmospheric pressure or under the 45 inherent pressure of the reaction mixture in question.

~. ~

3g Working-up of the reaction mixtures is generally carried out by methods known per se, for example by removing the solvent, partitioning the residue in a mixture of water and a suitable organic solvent and working up the organic phase to obtain the 5 product.

The 3-(4-cyanophenyl)uracils of the formula I can have one or more chiral centers, in which case they are usually obt~ine~ as enantiomer or diastereomer mixture~. If desired, the mixtures can 10 be ~eparated into the essentially pure isomers by customary methods, for example by means of crystallization or chromatography on an optically active adsorbate. Pure optically active isomers can, for example, also be prepared from the corresponding optically active starting materials.
3-(4-Cyanophenyl)uracils I where A is hydrogen can be converted into their salts, prefera~ly their alkali metal salts, in a manner known per se (cf., in this context, also preparation method b)).
Salts of I whose metal ion is other than an alkali metal ion can be prepared in the customary manner by double decomposition of the corresponding alkali metal salt, and ammonium, phosphonium, sulfonium and sulfoxonium salts by means of ammonia, phosphonium 25 hydroxides, sulfonium hydroxides or sulfoxonium hydroxides.

The compounds I and their agriculturally useful salts, in the form of the isomer mixtures and of the pure isomers, are suitable as herbicides. The herbicidal compositions comprising I provide 30 very effective control of vegetation on non-crop areas, particularly at high application rates. They act against broad-leaved weeds and grass weeds in crop~ such as wheat, rice, maize, soybeans and cotton without damaging the crop plants considerably. Thi~ effect is particularly pronounced at low 35 application rates.

Depending on the application method in question, the compounds I
or the herbicidal compositions comprising them can additionally be used in a further number of crop plants for eliminating 40 undesirable plants. Suitable crops are, for example, the following:
Allium cepa, Ananas comosus, Arachi~ hypogaea, Asparagus officinalis, Beta vulgaris ssp. altissima, Beta vulgaris ssp.
rapa, Brassica napus var. napus, Brassica napus var.
45 napobrassica, Brassica rapa var. silvestris, Camellia sinensis, Carthamus tinctorius, Carya illinoinensis, Citrus limon, Citrus sinen~is, Coffea arabica (Coffea canephora, Coffea liberica), '' 0050/45615 Cucumis sativus, Cynodon dactylon, Daucus carota, Elaeis guineensis, Fragaria vesca, Glycine max, Gossypium hirsutum, (Gossypium arboreum, Gossypium herbaceum, Gossypium vitifolium), Helianthus annuus, Hevea brasiliensis, Hordeum vulgare, Humulus 5 lupulus, Ipomoea batatas, Juglans regia, Lens culinaris, Linum usitatissimum, Lycopersicon lycopersicum, Malus spp., Manihot esculenta, Medicago sativa, Musa spp., Nicotiana tabacum (N.rustica), Olea europaea, Oryza sativa , Phaseolus lunatus, Phaseolus vulgaris, Picea abies, Pinus Bpp ., Pisum sativum, 10 Prunus avium, Prunus persica, Pyrus communis, Ribes sylvestre, Ricinus communis, Saccharum officinarum, Secale cereale, Solanum tuberosum, Sorghum bicolor (S. vulgare), Theobroma cacao, Trifolium pratense, Triticum aestivum, Triticum durum, Vicia faba, Vitis vinifera and Zea mays.
In addition, the compounds I can also be used in crops which tolerate the action of herbicides as a result of breeding, including genetic engineering methods.

20 Moreover, the 3-(4-cyanophenyl)uracils I are also suitable for the desiccation and/or defoliation of plants.

As desiccants, they are particularly suitable for desiccating the aerial parts of crop plants such as potatoes, oilseed rape, 25 sunflowers and soybeans. This allows completely mechanical harvesting of these important crop plants.

Al~o of economic interest i~ facilitating harvesting, which is made possible by concentrating, over a period of time, the drop 30 or the reduction of adhesion to the tree of citrus fruit, olives or other species and varieties of pomaceous fruit, stone fruit and shell fruit. The same mechanism, ie. promotion of the formation of abscission tissue between fruit or leaf and shoot of the plants, is also essential for the targeted controllable 35 defoliation of economic plants, in particular cotton.
Moreover, shortening the period of time within which the individual cotton plants mature results in an increased fiber quality post-harvest.
The compounds I, or the compositions comprising them, can be applied, for example, in the form of-ready-to-spray aqueous solutions, powders, suspensions, also highly concentrated aqueous oily or other suspensions or dispersions, emulsions, oil 45 dispersions, pastes, dust~, materials for spreading, or granules, by means of spraying, atomizing, dusting, scattering or pouring.
The use forms depend on the intended purposes; in any case, they 0050/45615 CA 022l0909 l997-07-30 should guarantee the finest possible distribution of the active ingredients according to the invention.

Suitable inert additives for the preparation of ready-to-spray 5 solutions, emulsions, pastes or oil dispersions are essentially:
mineral oil fractions of medium to high boiling point, such as kerosene and diesel oil, furthermore coal tar oils and oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbon~, eg. paraffins, tetrahydronaphthalene, alkylated 10 naphthalenes and their derivatives, alkylated benzenes and their derivatives, alcohols, such as methanol, ethanol, propanol, butanol and cyclohexanol, ketones, such as cyclohexanone, strongly polar solvents, eg. amines, such as N-methylpyrrolidone, and water.
Aqueous use forms can be prepared from emulsion concentrates, suspensions, pastes, wettable powders or water-dispersible granules by adding water. To prepare emulsions, pastes or oil dispersions, the substrates, either as such or dissolved in an 20 oil or solvent, can be homogenized in water by means of a wetting agent, tackifier, dispersant or emulsifier. Alternatively, it is possible to prepare concentrates comprising active ingredient, wetting agent, tackifier, dispersant or emulsifier and, if desired, solvent or oil, and these concentrates are suitable for 25 dilution with water.

Suitable surfactants (adjuvants) are the alkali metal salts, alkaline earth metal salts and ammonium salts of aromatic sulfonic acids, eg. ligno-, phenol-, naphthalene- and 30 dibutylnaphthalenesulfonic acid, or-of fatty acids, alkyl- and alkylaryl sulfonate~, alkyl, lauryl ether and fatty alcohol sulfates, and salts of sulfated hexa-, hepta- and octadecanols, and also of fatty alcohol glycol ethers, condensates of sulfonated naphthalene and its derivatives with formaldehyde, 35 condensates of naphthalene or of the naphthalenesulfonic acids with phenol and formaldehyde, polyoxyethylene octylphenol ether, ethoxylated isooctyl-, octyl- or nonylphenol, alkylphenyl polyglycol ethers, tributylphenyl polyglycol ether, alkylaryl polyether alcohols, isotridecyl alcohol, fatty alcohol/ethylene 40 oxide condensates, ethoxylated castor oil, polyoxyethylene alkyl ethers or polyoxypropylene alkyl ethers, lauryl alcohol polyglycol ether acetate, sorbitol esters, lignosulfite waste li~uors or methylcellulose.

g2 Powders, materials for spreading and dusts can be prepared by mixing or grinding the active ingredients together with a solid carrier.

5 Granules, eg. coated granules, impregnated granules and homogeneous granules, can be prepared by binding the active ingredients to solid carriers. Solid carriers are mineral earths, such as silicas, silica gels, silicates, talc, kaolin, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, 10 calcium sulfate, magnesium sulfate, magnesium oxide, ground synthetic materials, fertilizers, such as ammonium sulfate, ammonium phosphate, ammonium nitrate, urea, and products of vegetable origin, such as cereal meal, tree bark meal, wood meal and nutshell meal, cellulose powder, or other solid carriers.
The concentrations of the active ingredients I in the ready-to-use products can be varied within wide ranges. In general, the formulations comprise from 0.001 to 98% by weight, preferably from 0.01 to 95% by weight, of active ingredient. The 20 active ingredients are employed in a purity of from 90% to 100%, preferably 95% to 100% (in accordance with NMR spectrum).

The formulation examples which follow illustrate the preparation of such products:
I. 20 parts by weight of Compound No. I.01 are dissolved in a mixture composed of 80 parts by weight of alkylated benzene, 10 parts by weight of the adduct of 8 to 10 mol of ethylene oxide to 1 mol of oleic acid N-monoethanolamide, 5 parts by weight of calcium dodecylbenzenesulfonate and 5 parts by weight of the adduct of 40 mol of ethylene oxide to 1 mol of castor oil. Pouring the solution into 100,000 parts by weight of water and finely distributing it therein gives an aqueous dispersion comprising 0.02% by weight of the active ingredient.

II. 20 parts by weight of Compound No. I.02 are dissolved in a mixture composed of 40 parts by weight of cyclohexanone, 30 parts by weight of i~obutanol, 20 parts by weight of the adduct of 7 mol of ethylene oxide to 1 mol of isooctyl phenol and 10 parts by weight of the adduct of 40 mol of ethylene oxide to 1 mol of castor oil. Pouring the solution into 100,000 parts by weight of water and finely distributing it therein gives an aqueous dispersion comprising 0.02% by weight of the active ingredient.

III. 20 parts by weight of the active ingredient No. I.03 are dissolved in a mixture composed of 25 parts by weight of cyclohexanone, 65 parts by weight of a mineral oil fraction of boiling point 210 to 280 C and 10 parts by weight of the adduct of 40 mol of ethylene oxide to 1 mol of castor oil.
Pouring the solution into 100,000 parts by weight of water and finely distributing it therein gives an aqueous dispersion comprising 0.02~ by weight of the active ingredient.
IV. 20 parts by weight of the active ingredient No. I.04 are mixed thoroughly with 3 parts by weight of sodium diisobutylnaphthalene-a-sulfonic acid, 17 parts by weight of the sodium salt of a lignosulfonic acid from a sulfite waste liquor and 60 parts by weight of pulverulent silica gel, and the mixture is ground in a hA -r mill. Finely distributing the mixture in 20,000 parts by weight of water gives a spray mixture comprising 0.1% by weight of the active ingredient.
V. 3 parts by weight of the active ingredient No. I.05 are mixed with 97 parts by weight of finely divided kaolin.
This gives a dust comprising 3~ by weight of the active ingredient.
VI. 20 parts by weight of the active ingredient No. I.06 are mixed intimately with 2 parts by weight of calcium dodecylbenzenesulfonate, 8 parts by weight of fatty alcohol polyglycol ether, 2 parts by weight of the sodium salt of a phenol/urea/formaldehyde condensate and 68 parts by weight of a paraffinic mineral oil. This gives a stable oily dispersion.

VII. 1 part by weight of Compound No. I.07 is dissolved in a mixture composed of 70 parts by weight of cyclohexanone, 20 parts by weight of ethoxylated isooctylphenol and 10 parts by weight of ethoxylated castor oil. This gives a stable emulsion concentrate.
40 VIII. 1 part by weight of Compound No. I.08 is dissolved in a mixture composed of 80 parts by weight of cyclohexanone and 20 parts by weight of Emulphor EL1). This gives a stable emulsion concentrate.

45 1) ethoxylated castor oil The active ingredients I, or the herbicidal compositions, can be applied pre- or post-emergence. If the active ingredients are less well tolerated by certain crop plants, application techniques may be used where the herbicidal compositions are 5 sprayed, with the aid of the spraying equipment, in such a way that the active ingredients come into as little contact as possible with the leaves of the sensitive crop plants while reaching the leaves of undesirable plants which grow thereunder, or the naked soil surface (post-directed, lay-by).
The application rates of active ingredient I are from 0.001 to 3.0, preferably 0.01 to 1, kg of active ingredient (a.i.) per ha, depending on the desired control, the season, the target plants and the growth stage.
To widen the spectrum of action and to achieve synergistic effects, the 3-(4-cyanophenyl)uracils I may be mixed with a large number of representatives of other groups of herbicidal or growth-regulating active ingredients and then applied 20 concomitantly. Suitable components for mixtures are, for example, 1,2,4-thiadiazoles, 1,3,4-thiadiazoles, amides, aminophosphoric acid and derivatives thereof, aminotriazoles, anilides, aryloxy-/hetaryloxyalkanoic acids and derivatives thereof, benzoic acid and derivatives thereof, benzothiadiazinones, 25 2-(hetaroyl/aroyl)-1,3-cyclohexanediones, heteroaryl aryl ketones, benzylisoxazolidinones, meta-CF3-phenyl derivatives, carbamates, quinolinecarboxylic acid and derivatives thereof, chloroacetanilides, cyclohexane-1,3-dione derivatives, diazines, dichloropropionic acid and derivatives thereof, dihydrobenzo-30 furans, dihydrofuran-3-one, dinitroanilines, dinitrophenols, diphenyl ethers, dipyridylium compounds, halocarboxylic acids and derivatives thereof, ureas, 3-phenyluracils, imidazoles, imidazolinones, N-phenyl-3,4,5,6-tetrahydrophthalimides, oxadiazoles, oxiranes, phenols, aryloxy- and 35 heteroaryloxyphenoxypropionic esters, phenylacetic acid and derivatives thereof, 2-phenylpropionic acid and derivatives thereof, pyrazoles, phenylpyrazoles, pyridazines, pyridinecarboxylic acid and derivatives thereof, pyrimidyl ethers, sulfonamides, sulfonylureas, triazines, triazinones, 40 triazolinones, triazolecarboxamides and uracils.

It may furthermore be advantageous to apply the compounds I, alone or in combination with other herbicides, together with further crop protection agents, for example with pesticides or 45 agents for controlling pests, phytopathogenic fungi or bacteria.
Also of interest is the miscibility with mineral salt solutions, which are employed for treating nutrient and trace element ' ' 0050/45615 CA 02210909 1997-07-30 deficiencies. Nonphytotoxic oils and oil concentrates may also be added.

Preparation Examples Example 1 3-[4-Cyano-3-methoxyphenyl]-6-trifluoromethyl-1,2,3,4-tetrahydro-pyrimidine-2,4-dione (Comp. 1.01) 10 Sodium methanolate solution (2.8 g of a 30 percent strength solution in methanol) was added to a solution of 3-[4-cyano-3-nitrophenyl]-6-trifluoromethyl-l~2~3~4-tetrahydro-pyrimidine-2,4-dione (2.4 g) in 50 ml of anhydrou~ methanol. The reaction mixture was subsequently refluxed for 5 hours. After 15 cooling, water (50 ml) was added first, followed by 10~ strength aqueous hydrochloric acid to a pH of 3-4. The precipitate formed was 6ubsequently separated off, washed with water and petroleum ether and dried. Yield: 1.1 g; m.p.: >230 C.

20 Example 2 1-Amino-3-[4-cyano-3-methoxyphenyl]-6-trifluoromethyl-1,2,3,4-tetrahydropyrimidine-2,4-dione (Comp. 1.02) Potassium carbonate (1.0 g) and 2,4-dinitrophenoxyamine (0.8 g) 25 were added to a solution of 3-[4-cyano-3-methoxyphenyl]-6-trifluoromethyl-1,2,3,4-tetrahydro-pyrimidine-2,4-dione (1.1 g) in 15 ml of ethyl acetate. The mixture was subsequently stirred for 15 hours at 55-60 C, whereupon the solids formed were separated off and washed using 30 in each case 30 ml of ethyl acetate and diisopropyl ether. The combined filtrate~ were washed twice using in each case 25 ml of water, dried over sodium sulfate and then concentrated. After crystallization using 10 ml of diisopropyl ether, 0.6 g of the desired product was obtained. M.p.: >230 C.
Example 3 1-Amino-3-[4-cyano-3-hydroxyphenyll-6-trifluoromethyl-1,2,3,4-tetrahydropyrimidine-2,4-dione (Comp. 1.07) 40 1-Amino-3-[4-cyano-3-methoxyphenyl~-6-trifluoromethyl-1,2,3,4-tetrahydropyrimidine-2,4-dione (2.0 g) and pyridinium hydrochloride (2.1 g) were stirred for 2 hours at 200-210 C. After cooling, the reaction mixture was dissolved in 100 ml of n-butanol, whereupon the solution was washed three times using in 45 each case 30 ml of water. The organic phase was dried over sodium sulfate and ~ubsequently freed from solvent. After crystallization using 10 ml of diisopropyl ether and '' 0050/45615 chromatographic purification of the crude product ~eluent:
dichloromethane/ethyl acetate = 9:1 to 1:1~, 0.4 q of the desired product was obtained. M.p.: > 230 C.

5 Example 4 3-~3-Allyloxy-4-cyanophenyl]-1-methyl-6-trifluoromethyl-1,2,3,4-tetrahydropyrimidine-2,4-dione (Comp. 1.08) Potassium carbonate (4.6 g) and methyl iodide (2.1 ml, dissolved 10 in 20 ml of dimethylformamide) were added to a solution of 3-[3-allyloxy-4-cyanophenyl]-1-methyl-6-trifluoromethyl-1,2,3,4-tetrahydropyrimidine-2,4-dione (10.1 g) in 130 ml of dimethylformamide. After the reaction mixture had been stirred for 20 hours at room temperature, 150 ml of water were added, lS whereupon the precipitate formed was separated off, washed with water and petroleum ether and dried. Yield: 2.5 g;
m.p.: 158-160~C.

In addition to those mentioned above, other 20 3-(4-cyanophenyl)uracils I which were prepared, or can be prepared, in a similar ~nner are listed in Table 2 below:

A o R1 R2 ~ N~ CN

R3 Y oR4 30 No. Y A Rl R2 R3 R4 M.p. [ Cl 1.01 o H H CF3 H CH3 >230 -1.02 ~ NH2 H CF3 H CH3 ~230 1.03 o H H CF3 H CH2CH=CH2 208-210 35 1.04 ~ NH2 H CF3 H CH2CHzCH2 177-179 1.05 ~ CH3 H CF3 H CH3 >230 1.06 O H H CF3 H CH(CH3)2 180-184 1.07 ~ NH2 H CF3 H H >230 40 1.08 ~ CH3 H CF3 H CH2CH=CH2 158-1600 l.09 ~ NH2 H CF3 H CH~CH3)2 185-187 l.10 o H H CF3 H C2Hs >2~0 Preparation of the starting compounds:

Example 5 3-[4-cyano-3-nitrophenyl]-6-trifluoromethyl-1,2,3,4-tetrahydro-5 pyrimidine-2,4-dione Potassium carbonate (16.6 g) and potassium cyanide (7.8 g) were added to a solution of 3-l4-fluoro-3-nitrophenyl]-6-trifluoromethyl-1,2,3,4-tetrahydro-- 10 pyrimidine-2,4-dione (31.9 g) in 250 ml of anhydrous N,N-dimethylformamide. The reaction mixture was subsequently stirred for a total of 45 hours at 75-80 C, with two further additions of potassium cyanide (in total 4.6 g) since the reaction had not proceeded completely. For working-up, water 15 (250 ml) was added to the reaction mixture after it had cooled.
The pH was subsequently brought to 2-3 by adding 60 ml of 1 N
hydrochloric acid. After nitrogen had been passed through the mixture for 4 hours to expel the hydrocyanic acid which had been liberated, the precipitate formed was separated off, washed with 20 water and petroleum ether and dried. Yield: 17.0 g; m.p.: 135 C.

Example 6 3-[4-Cyano-2-fluoro-5-nitrophenyll-1-methyl-6-trifluoromethyl-1,2,3,4-tetrahydropyrimidine-2,4-dione (Comp. 8.2) Potassium cyanide (0.5 g) was added to a solution of 3-12,4-difluoro-5-nitrophenyl]-1-methyl-6-trifluoromethyl-1,2,3,4-tetrahydropyrimidine-2,4-dione (2.5 g) in 50 ml of anhydrous dimethyl sulfoxide. The reaction mixture was 30 subsequently stirred for 10 hours at room temperature, more potassium cyanide (0.16 g) being added after 5 hours. For working-up, most of the solvent was removed at 80 C under a high vacuum. The residue was taken up in lS0 ml of water, washed three times using in each case 30 ml of water, dried over Rodium 35 sulfate and concentrated. Chromatography on silica gel (dichloromethane aR eluent) and crystallization using petroleum ether gave 1.2 g of the de~ired product; m.p.: 155-157 C.

The following compounds of Table 3 were prepared in a similar 40 manner:

R2 ~ CN VIII

No. y A Rl R2 R~ M.p. [ C]
10 8.1 O H H CF3 H 135 8.2 ~ CH3 F CF3 H 155-157 8.3 O H F CF3 H 135-137 Use Examples (herbicidal activity) The herbicidal action of the 3-(4-cyanophenyl)uracils I was demonstrated by the following greenhouse experiments:

The culture containers used were plastic flower pots containing 20 loamy sand with approximately 3.0% of humus as the substrate. The seeds of the test plants were sown separately for each species.

In the case of the pre-emergence treatment, the active ingredients, which were suspended or emulsified in water, were 25 applied directly after sowing by means of finely distributing nozzles. The containers were irrigated gently to promote germination and growth and subsequently covered with translucent plastic hoods until the plants had rooted. This cover results in uniform germination of the test plants, unless this was adversely 30 affected by the active ingredients.

For the post-emergence treatment, the test plants were first grown to a plant height of 3 to 15 cm, depending on the growth form, and only then treated with the active ingredients which 35 were suspended or emulsified in water. The test plants were either sown directly and grown in the same containers, or grown separately as seedlings and transplanted to the test containers a few days prior to treatment. The application rate for the post-emergence treatment was 0.0156 or 0.0078 kg of a.i. (active 40 ingredient) per ha.

The plants were kept at from 10-25 C or 20-35 C, depending on the species. The test period extended to 2 - 4 weeks. During this time, the plants were tended and their response to individual 45 treatments was evaluated.

Evaluation was carried out using a scale from 0 to 100. 100 means no emergence of the plants, or complete destruction of at least the aerial parts, and 0 means no damage or normal course of growth.
s The plants used for the greenhouse experiments were the following species:

Scientific Name Common Name Abutilon theophrasti velvet leaf Galium aparine catchweed bedstraw Ipomoea subspecies morningglory Solanum nigrum black nightshade At an application rate of 0.0156 or 0.0078 kg of a.i./ha, compound No. I.02 was very effective against the abovementioned plants when used post-emergence.

20 Use examples (desiccant/defoliant activity) The test plants used were young cotton plants with 4 leaves (without cotyledons) which had been grown under greenhouse conditions (relative atmospheric humidity 50 to 70%; day/night 25 temperature = 27/20~C).

The young cotton plants underwent foliar treatment to runoff point with aqueous preparations of the active ingredients (with an addition of 0.15% by weight of the fatty alcohol alkoxylate 30 Plurafac LF 700 based on the spray mixture). The amount of water applied was 1000 l/ha (converted). After 13 days, the number of shed leaves and the degree of defoliation in % were deteL i~e~.

No leaves were shed in the untreated control plants.

Claims (20)

We claim:

1. A 3-(4-cyanophenyl)uracil of the general formula I

I

where the variables have the following meanings:
A is hydrogen, methyl or amino;
Y is oxygen or sulfur;
R1 is hydrogen or halogen;
R2 is hydrogen, halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkyltio, C1-C6-alkylsulfenyl or C1-C6-alkylsulfonyl;
R3 is hydrogen, halogen or C1-C6-alkyl;
R4 is hydrogen, C1-C6-haloalkyl, C1-C6-alkyl, C3-C8-cycloalkyl, C3-C6-alkenyl, C3-C6-alkynyl, (C1-C6-alkyl)-carbonyl, (C3-C6-alkenyl)carbonyl, (C3-C6-alkynyl)carbonyl or alkylsulfonyl, it being possible, if desired, for each of the last-mentioned 8 radicals to have attached to it one to three substituents, in each case selected from the group consisting of - halogen, nitro, cyano, hydroxyl, C3-C8-cycloalkyl, C1-C6-alkoxy, C3-C8-cycloalkoxy, C3-C6-alkenyloxy, C3-C6-alkyloxy, C1-C6-alkoxy-C1-C6-alkoxy, C1-C6-alkyltio, C1-C6-alkylsulfenyl, C1-C6-alkylsulfonyl, C1-C6-alkylideneaminoxy, - the phenyl, phenoxy or phenylsulfonyl group which can be unsubstituted or have attached to it one to three substituents, in each case selected from the group consisting of halogen, nitro, cyano, C1-C6-alkyl, C1-C6-alkoxy and C1-C6-haloalkyl, - a 3- to 7-membered heterocyclyl or heterocyclyloxy group having one to three hetero atoms selected from the group consisting of two oxygen atoms, two sulfur atoms and 3 nitrogen atoms, it being possible for the heterocycle to be saturated, partially or fully unsaturated or aromatic and, if desired, to have attached to it one to three substituents, in each case selected from the group consisting of halogen, nitro, cyano, C1-C6-alkyl, Cl-C6-alkoxy, C1-C6-haloalkyl and (C1-C6-alkyl)carbonyl, - a group -CO-XR5, -OCO-XR5 or -N(R5)R6 where X is a chemical bond, oxygen, sulfur or -N(R6)-;
R5 is hydrogen, C1-C6-alkyl, C3-C8-cycloalkyl, C3-C6-alkenyl, C3-C6-alkynyl, C1-C6-alkoxy-C1-C6-alkyl, (Cl-C6-alkoxy)-carbonyl-C1-C6-alkyl, phenyl or phenyl-C1-C6-alkyl, it being possible for the phenyl group and the phenyl ring of the phenylalkyl group to be unsubstituted or to have attached to it one to three radicals, in each case selected from the group consisting of halogen, nitro, cyano, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy and (C1-C6-alkyl)carbonyl or X and R5 together form a 3- to 7-membered heterocycle, bonded via nitrogen and having one to three hetero atoms selected from the group consisting of two oxygen atoms, two sulfur atoms and 3 nitrogen atoms, it being possible for the heterocycle to be saturated, partially or fully unsaturated or aromatic and, if desired, to have attached to it one to three substituents, in each case selected from the group consisting of halogen, nitro, cyano, C1-C6-alkyl, C1-C6-haloalkyl C1-C6-alkoxy and (C1-C6-alkyl)carbonyl;

and R6 represents hydrogen, hydroxyl, C1-C6-alkyl, C3-C8-cycloalkyl or C1-C6-alkoxy, or an agriculturally useful salt of a compound I where A is hydrogen.

2. A 3-(4-cyanophenyl)uracil of the formula I as claimed in claim 1 where the variables have the following meanings:

A is amino or methyl;
Y is oxygen;

R1 is hydrogen, fluorine or chlorine;

R2 is C1-C6-alkyl, C1-C6-haloalkyl or C1-C6-alkylsulfonyl;

R3 is hydrogen or halogen;

R4 is hydrogen, C1-C6-haloalkyl, C1-C6-alkyl, C3-C8-cycloalkyl, C3-C6-alkenyl, C3-C6-alkynyl, (C1-C6-alkyl)-carbonyl, (C3-C6-alkenyl)carbonyl or (C3-C6-alkynyl)-carbonyl, it being possible, if desired, for each of the last-mentioned 8 radicals to have attached to it one or two substituents, in each case selected from the group consisting of halogen, nitro, cyano, hydroxyl, C3-C8-cycloalkyl,C1-C6-alkoxy,C3-C8-cycloalkoxy, C3-C6-alkenyloxy, C3-C6-alkynyloxy, C1-C6-alkoxy-C1-C6-alkoxy, C1-C6-alkylthio, C1-C6-alkylsulfenyl, C1-C6-alkylsulfonyl, C1-C6-alkylideneaminoxy, -Co-X(R5), -OCO-XR5 or -N(R5)R6, where X is a chemical bond, oxygen, sulfur or -N(R6)-, R5 is hydrogen, C1-C6-alkyl, C3-C8-cycloalkyl, C3-C6-alkenyl, C3-C6-alkynyl, C1-C6-alkoxy-C1-C6-alkyl or (C1-C6-alkoxy)-carbonyl-C1-C6-alkyl, and R6 is hydrogen, hydroxyl, C1-C6-alkyl, C3-C8-cycloalkyl or C1-C6-alkoxy.

3. A 3-(4-cyanophenyl)uracil of the formula I as claimed in claim 1 where the variables have the following meanings;
A is amino or methyl;

Y is oxygen;

R1 is hydrogen or fluorine;

R2 is C1-C6-haloalkyl;

R3 is hydrogen, chlorine or bromine;

R4 is hydrogen, C1-C4-alkyl, C3-C6-cycloalkyl, C3-C4-alkenyl, C3-C4-alkynyl, C1-C4-cyanoalkyl, C1-C4-haloalkyl, C1-C4-alkyl-C1-C4-alkyl, (C1-C4-alkyl)carbonyl, -CH2-CO-XR5 or -CH(CH3)-CO-XR5;

X is a chemical bond, oxygen or -N(R6)-;

R5 is hydrogen, C1-C6-alkyl, C3-C8-cycloalkyl, C1-C6-alkoxy-C1-C6-alkyl or (C1-C6-alkoxy)carbonyl-C1-C6-alkyl;

R6 is hydrogen, C1-C6-alkyl or C1-C6-alkoxy.

4. A 3-(4-cyanophenyl)uracil of the formula I as claimed in claim 1 where A is amino.

5. A 3-(4-cyanophenyl)uracil of the formula I as claimed in claim 1 where A is hydrogen or methyl.

6. A 3-(4-cyanophenyl)uracil of the formula I as claimed in claim 1 where Y is oxygen.

7. A 3-(4-cyanophenyl)uracil of the formula I as claimed in claim 1 where R1 is hydrogen or fluorine.

8. A 3-(4-cyanophenyl)uracil of the formula I as claimed in claim 1, where R2 is C1-C4-haloalkyl.

9. A 3-(4-cyanophenyl)uracil of the formula I as claimed in claim 1, where R2 is trifluoromethyl or chlorodifluoromethyl.

10. A 3-(4-cyanophenyl)uracil of the formula I as claimed in claim 1, where R4 is C1-C4-alkyl, C1-C4-cyanoalkyl, C3-C4-alkynyl or (C1-C4-alkoxy)carbonyl-C1-C4-alkyl.

11. An enamine ester of the formula III

III

where L1 is C1-C6-alkyl or phenyl and the substituents A and R1 to R4 have the meanings given in claim 1.

12. An enamine carboxylate of the formula IV

IV

where L1 is C1-C6-alkyl or phenyl and the substituents A and R1 to R4 have the meanings given in claim 1.

13. The use of the 3-(4-cyanophenyl)uracils of the formula I and of the agriculturally useful salts of I as claimed in claim 1 as herbicides or for the desiccation and/or defoliation of plants.

14. Herbicidal composition comprising a herbicidally effective amount of at least one 3-(4-cyanophenyl)uracil of the formula I or of an agriculturally useful salt of I as claimed in claim 1 and at least one inert liquid and/or solid carrier and, if desired, at least one surfactant.

15. A composition for the desiccation and/or defoliation of plants comprising such an amount of at least one 3-(4-cyanophenyl)uracil of the formula I or of an agriculturally useful salt of I as claimed in claim 1 that it acts as a desiccant and/or defoliant, and at least one inert liquid and/or solid carrier and, if desired, at least one surfactant.

16. A process for the preparation of herbicidally active compositions, which comprises mixing a herbicidally active amount of at least one 3-(4-cyanophenyl)uracil of the formula I or of an agriculturally useful salt of I as claimed in claim 1 and at least one inert liquid and/or solid carrier, and, if desired, at least one surfactant.

17. A process for the preparation of compositions which act as desiccants and/or defoliants, which comprises mixing such an amount of at least one 3-(4-cyanophenyl)uracil of the formula I or of an agriculturally useful salt of I as claimed in claim 1 that it acts as a desiccant and/or defoliant, and at least one inert liquid and/or solid carrier, and, if desired, at least one surfactant.

18. A method of controlling undesirable vegetation, which comprises allowing a herbicidally active amount of at least one 3-(4-cyanophenyl)uracil of the formula I or of an agriculturally useful salt of I as claimed in claim l to act on plants, their environment or on seed.

19. A method of desiccating and/or defoliating plants, which comprises applying to plants such an amount of at least one 3-(4-cyanophenyl)uracil of the formula I or of an agriculturally useful salt of I as claimed in claim 1 that it acts as a desiccant and/or defoliant.

20. A process for the preparation of 3-(4-cyanophenyl)uracils of the formula I as claimed in claim 1, which comprises either a) cyclizing an enamine ester of the formula III

III

or an enamine carboxylate of the formula IV

IV;

b) methylating or aminating a 3-(4-cyanophenyl)uracil of the formula I where A is hydrogen;

c) treating a 3-(4-cyanophenyl)uracil of the formula I where Y is oxygen with a sulfating reagent;
d) substituting the halide in compounds of the formula V

V

by cyanide;

e) halogenating a 3-(4-cyanophenyl)uracil of the formula I
where R3 is hydrogen;
f) alkylating or acylating a 3-(4-cyanophenyl)uracil of the formula I where R4 is hydrogen;

g) subjecting a 3-(4-cyanophenyl)uracil of the formula I
where R4 is other than hydrogen to ether or ester cleavage;
h) nitrating a 3-(4-halophenyl)uracil of the formula VIII

VIII, subsequently substituting the halogen atom by cyano and the nitro group by ~OR4;
i) or nitrating a phenyl compound of the formula X

X, subsequently reducing the nitro group to the amino group and then converting the latter into the cyano group by the method ofSandmeyer..