N-ACYLIMINO HETEROCYCLIC COMPOUNDS AND THEIR USE

AS PESTICIDES

The present invention relates to N-acylimino heterocyclic compounds, including their stereoisomers, tautomers and salts, and to compositions comprising such compounds. The invention also relates to the use of the N-acylimino heterocyclic compounds, their

stereoisomers, their tautomers and their salts, for combating invertebrate pests. Furthermore the invention relates also to methods of combating invertebrate pests, which comprises applying such compounds. Background of Invention

Invertebrate pests, such as insects, acaridae and nematode pests destroy growing and harvested crops and attack wooden dwelling and commercial structures, causing large economic loss to the food supply and to property. While a large number of pesticidal agents are known, due to the ability of target pests to develop resistance to said agents, there is an ongoing need for new agents for combating animal pests. In particular, animal pests such as insects and acaridae are difficult to be effectively controlled.

EP 259738 discloses co ula A, which have insecticidal activity:

(A)

where W is a substituted pyridyl radical or a 5-or 6-membered heterocyclic radical, R is hydrogen or alkyl, T together with the atoms to which it is bound forms a 5- or 6-membered heterocyclic ring, Y is inter alia a nitrogen atom and Z is an electron withdrawing group selected from nitro and cyano.

Pesticidal compounds, which are similar to those of EP 259738, are known from

EP 639569, where the moiety electron withdrawing moiety Z is an electron withdrawing group such as alkoxcarbonyl, arylcarbonyl, heterocyclic carbonyl, Ci-C4-alkylsulfonyl, sulfamoyl or

US 2013/0150414 describe, inter alia, pesticidal compounds of the formula B

wherein Ar is an aryl or 5- or 6-membered heterocyclic group, R _a is hydrogen or alkyi, Y' is hydrogen, halogen, a hydroxyl group, an alkyi group or an alkoxy group and Rb is an alkyi group substituted with halogen or an alkoxy group, optionally substituted with halogen.

Pesticidal compounds, which are similar to those of US 2013/0150414, are known from

WO 2013/129688.

PCT/EP2014/068415 (earlier filed US provisional application 61/871892, filed August 30, 2013) describes compounds similar to the compounds of formula (B), where Ar is an optionally 3-tetrahydrofuryl radical and Rb is a heterocyclic radical.

The pesticidal activity of the compounds is not satisfactory. It is therefore an object of the present invention to provide compounds having a good pesticidal activity, especially against difficult to control insects and acarid pests.

Summary of Invention

It has been found that these objects are solved by N-substituted acyl-imino compounds of the general formula (I) described below, by their stereoisomers, their tautomers and their salts. Therefore, the present invention relates to N-acylimino compounds of formula (I):

wherein is O or S; is selected from the group consisting of

linear Ci-C6-alkanediyl, which is unsubstituted or substituted with 1 to 6 identical or different radicals R ^D1 ,

linear C2-C6-alkenediyl, which is unsubstituted or substituted with 1 to 6 identical or different radicals R ^D1 ,

linear C2-C6-alkynediyl, which is unsubstituted or substituted with 1 to 6 identical or different radicals R ^D1 ,

C3-C6-cycloalkanediyl, which is unsubstituted or substituted with 1 to 6 identical or different radicals R ^D2 ,

C3-C6-cycloalkenediyl, which is unsubstituted or substituted with 1 to 6 identical or different radicals R ^D2 ,

saturated or partially unsaturated 3- to 7-membered heterocyclodiyl, which is unsubstituted or substituted with 1 , 2, 3, 4, 5 or 6 radicals R ^D2 ,

phenylene, which is unsubstituted or substituted with 1 , 2, 3 or 4 radicals R ^D3 , and

5- or 6-membered hetarylene, which is unsubstituted or substituted with 1 , 2 or 3 radicals R ^D3 ; where

R ^D1 is selected from the group consisting of cyano, halogen, azido, nitro, -SCN, SF ₅ , d-Ce-alkyl, Ci-C ₆ -haloalkyl, C ₃ -C ₈ -cycloalkyl, C ₃ -Ce-halocycloalkyl, C ₂ -C ₆ - alkenyl, C ₂ -C ₆ -haloalkenyl, C ₂ -C ₆ -alkynyl, C ₂ -C ₆ haloalkynyl, Si(R ¹¹ ) ₂ R ¹² , OR ⁸ , OS0 ₂ R ⁸ , S(0) _n R ⁸ , S(0) _n NR ^7a R ^7b , NR ^17a R ^17b , C(=0)NR ^7a R ^7b ,

C(=S)NR ^7a R ^7b , C(=0)OR ⁸ , C(=0)R ¹⁵ , C(=S)R ¹⁵ , C(=NR ⁷ )R ¹⁵ , NR ^7a - C(=0)R ^7a , NR ^7a -C(=S)R ^7a , NR ^7a -C(=0)OR ⁸ , NR ^7a -C(=0)NR ^7a R ⁷ , phenyl, phenyl-Ci-C4-alkyl, where the phenyl ring in the last two groups is unsubstituted or substituted with 1 , 2, 3, 4 or 5 identical or different

substituents R ¹⁰ , and

a 3-, 4-, 5-, 6- or 7- membered saturated, partly saturated or unsaturated aromatic heterocyclic ring comprising 1 , 2 or 3 heteroatoms as ring members, which are identical or different and selected from oxygen, nitrogen and sulfur, where the heterocyclic ring is unsubstituted or substituted with 1 , 2, 3 or 4 identical or different substituents R ¹⁰ , and wherein the nitrogen and/or the sulfur atom(s) of the heterocyclic ring may optionally be oxidized,

or two R ^D1 present on one carbon atom may together form =0, =CR ¹³ R ¹⁴ , =S, =NR ¹⁷ , =NOR ¹⁶ , =NNR ^9a R ^9b ,

or two radicals R ^D1 , which are bound to the same carbon atom may, together with said carbon atom, form a 3- to 6-membered carbo- or heterocyclic ring, where the heterocyclic ring has 1 or 2 heteroatoms or heteroatom moieties as ring members which are selected from the group consisting of O, S, S(O), S(0)2 and N, where said carbo- or heterocyclic ring is unsubstituted or carry 1 , 2, 3 or 4 radicals selected from halogen, Ci-C6-alkyl, C2-C6-alkoxy, C3-C8- cycloalkyl, C2-C6-alkenyl, C2-C6-alkynyl, wherein the carbon atoms of the aforementioned aliphatic and cycloaliphatic radicals may be unsubstituted, partially or completely halogenated;

R ^D2 has one of the meanings given for R ^D1 or two radicals R ^D2 , which are bound to adjacent carbon atoms may, together with said carbon atoms, form a fused 3- to 6-membered carbo- or heterocyclic ring, where the heterocyclic ring has 1 or 2 heteroatoms or heteroatom moieties as ring members which are selected from the group consisting of O, S, S(O), S(0)2 and N, where said carbo- or heterocyclic ring is unsubstituted or carry 1 , 2, 3 or 4 radicals selected from halogen, Ci-C6-alkyl, C2-C6-alkoxy, Cs-Cs-cycloalkyl, C2-C6-alkenyl, C2-C6- alkynyl, wherein the carbon atoms of the aforementioned aliphatic and cycloaliphatic radicals may be unsubstituted, partially or completely

halogenated;

R ^D3 is selected from the group consisting of halogen, cyano, azido, nitro, SCN, SF ₅ , Ci-C6-alkyl, Cs-Cs-cycloalkyl, C2-C6-alkenyl, C2-C6-alkynyl, wherein the carbon atoms of the aforementioned aliphatic and cycloaliphatic radicals may optionally be substituted with 1 , 2, 3, 4 or 5 identical or different radicals R ⁷ , Si(R ¹¹ ) ₂ R ¹² , OR ¹⁶ , OS(0) _n R ¹⁶ , -S(0) _n R ¹⁶ , S(0) _n NR ^7a R ^7b , NR ^17a R ^17b , C(=0)R ¹⁵ , C(=S)R ¹⁵ , C(=0)OR ¹⁶ , -C(=NR ⁷ )R ¹⁵ , C(=0)NR ^7a R ^7b , C(=S)NR ^7a R ⁷ , phenyl, optionally substituted with 1 , 2, 3, 4 or 5 identical or different radicals selected from OH, halogen, cyano, nitro, Ci-C6-alkyl, Ci-C6-haloalkyl, C1-C6- alkoxy and Ci-C6-haloalkoxy, Y indicates O, S or N-R ⁵ ;

Het is a 5- or 6-membered carbon-bound or nitrogen-bound heterocyclic or

heteroaromatic ring, comprising 2, 3, 4 or 5 carbon atoms and 1 , 2 or 3 heteroatoms as ring members, which are independently selected from sulfur, oxygen or nitrogen, wherein the sulfur and nitrogen ring members can independently be partly or fully oxidized, and wherein each ring is optionally substituted by k identical or different substituents R ⁶ , wherein k is an integer selected from 0, 1 , 2, 3 or 4;

W ¹ -W ² -W ³ -W ⁴ represents a carbon chain group connected to N and C=N, and thus forming a saturated, unsaturated, or partially unsaturated 5 or 6 membered nitrogen containing heterocycle, wherein

W ¹ , W ² , W ³ and W ⁴ each individually represent CR ^V R ^W , wherein

each R ^w independently from each other, is hydrogen, halogen, cyano, azido, nitro,

SCN, SF ₅ , Ci-Cio-alkyl, C ₃ -C ₈ -cycloalkyl, C ₂ -Cio-alkenyl or C ₂ -Cio- alkynyl, wherein the carbon atoms of the aforementioned aliphatic and cycloaliphatic radicals may be unsubstituted or may be partly or fully halogenated and/or may optionally be substituted with 1 , 2 or 3 identical or different radicals R ⁷ ,

or R ^w is OR ⁸ , NR ^9a R ^9b , S(0) _n R ⁸ , S(0) _n NR ^9a R ^9b , C(=0)R ^7a , C(=0)NR ^9a R ^9b , C(=0)OR ⁸ , C(=S)R ^7a , C(=S)NR ^9a R ^9b , C(=S)OR ⁸ ,

C(=S)SR ⁸ , C(=NR ⁷ )R ^7a , C(=NR ⁷ )NR ^9a R ⁹ and Si(R ¹¹ ) ₂ R ¹² ,

each R ^v independently from each other, are selected from the group consisting of hydrogen, halogen, cyano, Ci-Cio-alkyl, Cs-Cs-cycloalkyl, C2-Cio-alkenyl and C2-Cio-alkynyl, wherein the carbon atoms of the aforementioned four aliphatic and cycloaliphatic radicals may be unsubstituted or may be partly or fully halogenated or may optionally be further substituted with 1 , 2 or 3 identical or different radicals R ⁷ ; or

R ^v and R ^w present in one of the groups may together form =0, =CR ¹³ R ¹⁴ , =S,

=NR ¹⁷ , =NOR ¹⁶ , =NNR ^9a R ⁹ ,

or

two R ^w of adjacent carbon atoms, may form both together and together with the existing bond a double bond between the adjacent carbon atoms; and wherein one of W ² or W ³ may optionally represent a single or a double bond between the adjacent carbon atoms;

R ¹ , R ² are independently from each other selected from the group consisting of hydrogen, halogen, CN, SCN, nitro, Ci-C6-alkyl, C3-C6-cycloalkyl, wherein each of the two aforementioned radicals are unsubstituted, partly or completely halogenated or may carry any combination of 1 , 2 or 3 radicals R ⁷ , Si(R ¹¹ ) ₂ R ¹² , OR ⁸ , OSO2R ⁸ , S(0) _n R ⁸ , S(0) _n NR ^9a R ^9b , NR ^9a R ^9b , C(=0)NR ^9a R ^9b , C(=S)NR ^a R , C(=0)OR ⁸ , C(=0)R ^7a , C(=S)R ^7a ,

phenyl, benzyl, where the phenyl ring in the last two radicals is unsubstituted or optionally substituted with 1 , 2, 3, 4 or 5 identical or different substituents R ¹⁰ ,

a 3-, 4-, 5-, 6- or 7- membered saturated, partly saturated or unsaturated aromatic heterocyclic ring comprising 1 , 2 or 3 identical or different heteroatoms as ring members, which are selected from oxygen, nitrogen and sulfur, where the heterocyclic ring is optionally substituted with 1 , 2, 3 or 4 identical or different substituents R ¹⁰ , and wherein the nitrogen and/or the sulfur atom(s) of the heterocyclic ring may optionally be oxidized, or

R ¹ and R ² form, together with the carbon atom, which they attached to, a 3-,

4-, 5- or 6-membered saturated or partly unsaturated carbocyclic or heterocyclic ring, wherein each of the carbon atoms of said cycle are unsubstituted or may carry any combination of 1 or 2 identical or different radicals R ⁷ ,

or

R and R ² may together be =0, =CR ¹³ R ¹⁴ , =S, =NR ¹⁷ , =NOR ¹⁶ or =NNR ^9a R ⁹ ; is selected from the group consisting of hydrogen, Ci-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, Cs-Cs-cycloalkyl, C3-C8-cycloalkyl-Ci-C4-alkyl, Ci-C6-alkyl-Z, C3-C8-cycloalkyl-Z, C2-C6-alkenyl-Z, C2-C6-alkynyl-Z, and

C3-C8-cycloalkyl-Ci-C4-alkyl-Z, wherein the carbon atoms of each of the 10 last mentioned radicals are unsubstituted, partly or completely halogenated, it being also possible for these radicals to carry 1 or 2 radicals R ⁷ , which are different from Ci-C6-alkyl, it being also possible for cycloalkyi radicals to carry 1 , 2, 3, 4, 5 or 6 Ci-C ₄ -alkyl groups; the moieties Q-phenyl, Q'-O-phenyl and Q'-S-phenyl, where the phenyl ring is optionally substituted with one or more, e.g. 1 , 2, 3, 4 or 5 identical or different substituents R ¹⁰ , and the moieties Q-Het ^# , Q'-0-Het ^# and Q'-S-Het ^# where

Z is O, S or N-R ^z ;

R ^z if present, is selected from the group consisting of hydrogen, CN, d-Ce-alkyl, C ₂ -C ₆ -alkenyl, C ₂ -C ₆ -alkynyl, C ₃ -C ₈ -cycloalkyl, C ₃ -C ₈ - cycloalkyl-Ci-C4-alkyl, Ci-C6-alkylcarbonyl, Ci-C6-alkylsulfonyl, Ci-C6-alkoxycarbonyl, wherein each of the eight last mentioned radicals are unsubstituted, partly or completely halogenated, phenyl, phenyl-Ci-C4-alkyl, phenylcarbonyl, phenoxycarbonyl or phenylsulfonyl, where the phenyl ring in the last 5 mentioned groups is unsubstituted or substituted with 1 , 2, 3, 4 or 5 identical or different substituents R ¹⁰ ;

Het ^# represents a 3-, 4-, 5-, 6- or 7- membered saturated, partly saturated or unsaturated aromatic heterocyclic ring comprising 1 , 2, 3 or 4 heteroatoms as ring members, which are selected from oxygen, nitrogen and/or sulfur, where the heterocyclic ring is optionally substituted with 1 , 2, 3 or 4 identical or different substituents R ¹⁰ , and wherein the nitrogen and/or the sulfur atom(s) of the heterocyclic ring may optionally be oxidized, and

Q, Q' irrespectively of their occurrence, are a single bond, Ci-C6-alkanediyl, C2-C6-alkenediyl, or C2-C6-alkynediyl, has one of the meanings given for R ³ ; or R ³ and R ⁴ together may also form a bivalent radical, selected from the group consisting of Cs-Ce-alkanediyl, C ₃ -C ₆ -alkenediyl, Q ¹ -C ₂ -C ₅ -alkanediyl, Q ¹ -C ₂ -C ₅ - alkenediyl, Q ¹ -C2-C4-alkanediyl-Q ² and Q ¹ -C2-C4-alkenediyl-Q ² , wherein the carbon atoms in the six aforementioned radicals are unsubstituted or may carry 1 , 2, 3 or 4 radicals R ^7b , and wherein Q ¹ and Q ² are, independently from each other, selected from O, S and N-R ^7d ; if present, is selected from the group consisting of hydrogen, CN, Ci-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, Cs-Cs-cycloalkyl, C3-C8-cycloalkyl-Ci-C4-alkyl, Ci-C6-alkylcarbonyl, Ci-C6-alkylsulfonyl, Ci-C6-alkoxycarbonyl, wherein each of the eight last mentioned radicals are unsubstituted, partly or completely halogenated,

phenyl, phenyl-Ci-C4-alkyl, phenylcarbonyl, phenoxycarbonyl and phenylsulfonyl, where the phenyl ring in the last five mentioned groups is unsubstituted or substituted with 1 to 5 identical or different substituents R ¹⁰ , or

R ³ and R ⁵ together may also form a bivalent radical, selected from the group consisting of C2-C6-alkanediyl and C2-C6-alkenediyl, wherein the carbon atom in the two aforementioned radicals are unsubstituted or may carry 1 to 6 radicals R ^7c ; where, independently of their occurrence, is 0, 1 or 2; is selected from the group consisting of halogen, cyano, azido, nitro, SCN, SF ₅ , Ci-Cio-alkyl, Cs-Cs-cycloalkyl, C2-Cio-alkenyl, C2-Cio-alkynyl, and wherein the carbon atoms of the last 4 aliphatic and cycloaliphatic radicals may be partially or completely halogenated and/or further substituted independently from one another with 1 , 2 or 3 radicals R ⁷ ,

OR ⁸ , NR ^17a R ^17b , S(0) _n R ⁸ , S(0) _n NR ^7a R ^7b , C(=0)R ^7a , C(=0)NR ^7a R ^7b , C(=0)OR ⁸ , C(=S)R ^7a , C(=S)NR ^7a R ⁷ , C(=S)OR ⁸ , C(=S)SR ⁸ , C(=NR ⁷ )R ^7a , C(=NR ⁷ )NR ^7a R ⁷ , Si(R ¹¹ ) ₂ R ¹² ;

phenyl, optionally substituted with 1 , 2, 3, 4 or 5 identical or different substituents a 3-, 4-, 5-, 6- or 7- membered saturated, partly saturated or unsaturated aromatic heterocyclic ring comprising 1 , 2 or 3 heteroatoms as ring members, which are identical or different and selected from oxygen, nitrogen and sulfur, where the heterocyclic ring is optionally substituted with 1 , 2, 3 or 4 identical or different substituents R ¹⁰ , and wherein the nitrogen and/or the sulfur atom(s) of the heterocyclic ring may optionally be oxidized,

or two of R ⁶ present on one ring carbon may together form =0, =CR ¹³ R ¹⁴ , =S, =NR ¹⁷ , =NOR ¹⁶ , =NNR ^9a R ^9b ,

or two R ⁶ together form a linear C2-C7 alkylene chain, thus forming, together with the ring atom(s) to which they are bound, a 3-, 4-, 5-, 6-, 7- or 8-membered ring, where 1 or 2 CH2 moieties of the alkylene chain may be replaced by 1 or 2 heteroatom moieties selected from O, S and NR ^17c and/or 1 or 2 of the CH2 groups of the alkylene chain may be replaced by a group C=0, C=S and/or C=NR ¹⁷ ; and where the alkylene chain is unsubstituted or may be substituted with 1 , 2, 3, 4, 5 or 6 radicals selected from the group consisting of halogen, Ci-C6-haloalkyl, C1-C6- alkoxy, Ci-C6-haloalkoxy, Ci-C6-alkylthio, Ci-C6-haloalkylthio, Cs-Cs-cycloalkyl, C3-C8-halocycloalkyl, C2-C6-alkenyl, C2-C6-haloalkenyl, C2-C6-alkynyl, C2-C6- haloalkynyl, phenyl which may be substituted with 1 , 2, 3, 4 or 5 radicals R ¹⁰ , and a 3-, 4-, 5-, 6- or 7-membered saturated, partially unsaturated or aromatic heterocyclic ring containing 1 , 2 or 3 heteroatoms or heteroatom groups selected from N, O, S, NO, SO and SO2, as ring members, where the heterocyclic ring may be substituted with 1 , 2, 3, 4 or 5 radicals R ¹⁰ ; independently of its occurrence, is selected from the group consisting of cyano, azido, nitro, -SCN, SF ₅ , d-C ₆ -alkyl, Ci-C ₆ -haloalkyl, C ₃ -C ₈ -cycloalkyl, C ₃ -C ₈ - halocycloalkyl, C2-C6-alkenyl, C2-C6-haloalkenyl, C2-C6-alkynyl, C2-C6 haloalkynyl, Si(R ¹¹ ) ₂ R ¹² , OR ⁸ , OSO2R ⁸ , S(0) _n R ⁸ , S(0) _n NR ^7a R ^7b , NR ^17a R ^17b , C(=0)NR ^7a R ^7b , C(=S)NR ^7a R ⁷ , C(=0)OR ⁸ , C(=0)R ¹⁵ , C(=S)R ¹⁵ , C(=NR ⁷ )R ¹⁵ , NR ^7a -C(=0)R ^7a , NR ^7a -C(=S)R ^7a , NR ^7a -C(=0)OR ⁸ , NR ^7a -C(=0)NR ^7a R ⁷ ,

phenyl, phenyl-Ci-C4-alkyl, where the phenyl ring in the last two groups is optionally substituted with 1 , 2, 3, 4 or 5 identical or different substituents R ¹⁰ , and

a 3-, 4-, 5-, 6- or 7- membered saturated, partly saturated or unsaturated aromatic heterocyclic ring comprising 1 , 2 or 3 heteroatoms as ring members, which are identical or different and selected from oxygen, nitrogen and sulfur, where the heterocyclic ring is optionally substituted with 1 , 2, 3 or 4 identical or different substituents R ¹⁰ , and wherein the nitrogen and/or the sulfur atom(s) of the heterocyclic ring may optionally be oxidized,

or two R ⁷ present on one carbon atom may together form =0, =CR ¹³ R ¹⁴ , =S, =NR ¹⁷ , =NOR ¹⁶ , =NNR ^9a R ^9b ,

or two R ⁷ may form a 3-, 4-, 5-, 6-, 7- or 8-membered saturated or partly unsaturated carbocyclic or heterocyclic ring together with the carbon atoms to which the two R ⁷ are bonded, where the heterocyclic ring comprises 1 , 2 or 3 heteroatoms as ring members, which are identical or different and selected from oxygen, nitrogen and sulfur, where the heterocyclic ring is optionally substituted with 1 , 2, 3 or 4 identical or different substituents R ¹⁰ ;

R ^7a independently of its occurrence, is selected from the group consisting of hydrogen, Ci-C6-alkyl, Ci-C6-haloalkyl, Ci-C6-alkoxy, Ci-C6-haloalkoxy, Ci-C6-alkylthio, C1-C6- alkylsulfinyl, Ci-C6-alkylsulfonyl, Ci-C6-haloalkylthio, Cs-Cs-cycloalkyl, C3-C8- halocycloalkyl, C2-C6-alkenyl, C2-C6-haloalkenyl, C2-C6-alkynyl, C2-C6 haloalkynyl, phenyl, optionally substituted with 1 , 2, 3, 4 or 5 identical or different substituents R ¹⁰ , and

a 3-, 4-, 5-, 6- or 7- membered saturated, partly saturated or unsaturated aromatic heterocyclic ring comprising 1 , 2 or 3 heteroatoms as ring members, which are identical or different and selected from oxygen, nitrogen and sulfur, where the heterocyclic ring is optionally substituted with 1 , 2, 3 or 4 identical or different substituents R ¹⁰ , and wherein the nitrogen and/or the sulfur atom(s) of the heterocyclic ring may optionally be oxidized; R ^7b independently of its occurrence, is selected from the group consisting of halogen,

Ci-C6-alkyl, Ci-C6-haloalkyl, Ci-C6-alkoxy, Ci-C6-haloalkoxy, Ci-C6-alkylthio, C1-C6- alkylsulfinyl, Ci-C6-alkylsulfonyl, Ci-C6-haloalkylthio, Cs-Cs-cycloalkyl, C3-C8- halocycloalkyl, C2-C6-alkenyl, C2-C6-haloalkenyl, C2-C6-alkynyl, C2-C6 haloalkynyl, phenyl, optionally substituted with 1 , 2, 3, 4 or 5 identical or different substituents R ¹⁰ , and

a 3-, 4-, 5-, 6- or 7- membered saturated, partly saturated or unsaturated aromatic heterocyclic ring comprising 1 , 2 or 3 heteroatoms as ring members, which are identical or different and selected from oxygen, nitrogen and sulfur, where the heterocyclic ring is optionally substituted with 1 , 2, 3 or 4 identical or different substituents R ¹⁰ , and wherein the nitrogen and/or the sulfur atom(s) of the heterocyclic ring may optionally be oxidized, or

two of R ^7b present on one carbon may together form =0, =CR ¹³ R ¹⁴ , =S, =NR ¹⁷ , =NOR ¹⁶ , =NNR ^9a R ^9b ; R ^7c independently of its occurrence, is selected from the group consisting of halogen,

Ci-C6-alkyl, Ci-C6-haloalkyl, Ci-C6-alkoxy, Ci-C6-haloalkoxy, Ci-C6-alkylthio, C1-C6- alkylsulfinyl, Ci-C6-alkylsulfonyl, Ci-C6-haloalkylthio, Cs-Cs-cycloalkyl, C3-C8- halocycloalkyl, C2-C6-alkenyl, C2-C6-haloalkenyl, C2-C6-alkynyl, C2-C6 haloalkynyl, phenyl, optionally substituted with 1 , 2, 3, 4 or 5 identical or different substituents R ¹⁰ , and

a 3-, 4-, 5-, 6- or 7- membered saturated, partly saturated or unsaturated aromatic heterocyclic ring comprising 1 , 2 or 3 heteroatoms as ring members, which are identical or different and selected from oxygen, nitrogen and sulfur, where the heterocyclic ring is optionally substituted with 1 , 2, 3 or 4 identical or different substituents R ¹⁰ , and wherein the nitrogen and/or the sulfur atom(s) of the heterocyclic ring may optionally be oxidized, or

two of R ^7c present on one carbon may together form =0, =CR ¹³ R ¹⁴ , =S, =NR ¹⁷ , =NOR ¹⁶ , =NNR ^9a R ^9b ; R ^7d is selected from the group consisting of hydrogen, CN, Ci-C6-alkyl, C2-C6-alkenyl,

C2-C6-alkynyl, Cs-Cs-cycloalkyl, C3-Cs-cycloalkyl-Ci-C4-alkyl, Ci-C6-alkylcarbonyl, Ci-C6-alkylsulfonyl, Ci-C6-alkoxycarbonyl, wherein each of the eight last mentioned radicals are unsubstituted, partly or completely halogenated,

phenyl, phenyl-Ci-C4-alkyl, phenylcarbonyl, phenoxycarbonyl and phenylsulfonyl, where the phenyl ring in the last five mentioned groups is unsubstituted or substituted with 1 to 5 identical or different substituents R ¹⁰ ,

R ⁸ independently of its occurrence, is selected from the group consisting of hydrogen, d-Ce-alkyl, Ci-C ₆ -haloalkyl, C ₃ -C ₈ -cycloalkyl, C ₃ -C ₈ -cycloalkyl-Ci-C ₄ -alkyl, C ₃ -C ₈ - halocycloalkyl, C2-C6-alkenyl, C2-C6-haloalkenyl, C2-C6-alkynyl, C2-C6 haloalkynyl,

C(=0)R ¹⁵ , C(=0)NR ^7a R ^7b , C(=S)NR ^7a R ⁷ , C(=0)OR ¹⁶ ,

phenyl, phenyl-Ci-C- ₄ -alkyl, where the phenyl ring in the last two mentioned radicals is unsubstituted or substituted with 1 , 2, 3, 4 or 5 identical or different substituents R ¹⁰ , and a 3-, 4-, 5-, 6- or 7- membered saturated, partly saturated or unsaturated aromatic heterocyclic ring comprising 1 , 2 or 3 heteroatoms as ring members, which are identical or different and selected from oxygen, nitrogen and sulfur, where the heterocyclic ring is optionally substituted with 1 , 2, 3 or 4 identical or different substituents R ¹⁰ , and wherein the nitrogen and/or the sulfur atom(s) of the heterocyclic ring may optionally be oxidized,

R ^9a , R ^9b are each independently from one another selected from the group consisting of hydrogen, Ci-C6-alkyl, Ci-C6-haloalkyl, Ci-C6-alkoxy, Ci-C6-haloalkoxy, Ci-C6-alkylthio, Ci-C6-haloalkylthio, Cs-Cs-cycloalkyl, Cs-Cs-halocycloalkyl,

C3-C8-cycloalkyl-Ci-C4-alkyl, C2-C6-alkenyl, C2-C6-haloalkenyl, C2-C6-alkynyl, C2-C6 haloalkynyl,

S(0) _n R ¹⁶ , -S(0) _n N R ^7a R ⁷ , C(=0)R ¹⁵ , C(=0)OR ¹⁶ , C(=0)N R ^7a R ⁷ , C(=S)R ¹⁵ , C(=S)SR ¹⁶ , C(=S)N R ^7a R ^7b , C(=N R ⁷ )R ¹⁵ ;

phenyl, benzyl, 1 -phenethyl or 2-phenethyl, where the phenyl ring in the last four mentioned radicals is unsubstituted or may be substituted with 1 , 2, 3, 4 or 5 identical or different substituents R ¹⁰ ; and

a 3-, 4-, 5-, 6- or 7- membered saturated, partly saturated or unsaturated aromatic C-bound heterocyclic ring comprising 1 , 2 or 3 heteroatoms as ring members, which are identical or different and selected from oxygen, nitrogen and sulfur, where the heterocyclic ring is optionally substituted with 1 , 2, 3 or 4 identical or different substituents R ¹⁰ , and wherein the nitrogen and/or the sulfur atom(s) of the heterocyclic ring may optionally be oxidized, or,

R ^9a and R ^9b are together a C2-C7 alkylene chain and form a 3-, 4-, 5-, 6-, 7- or 8- membered saturated, partly saturated or unsaturated aromatic ring together with the nitrogen atom they are bonded to, wherein the alkylene chain may contain one or two heteroatoms, which are, independently of each other, selected from oxygen, sulfur or nitrogen, and where the alkylene chain may optionally be substituted with 1 , 2, 3 or 4 radicals selected from halogen,

Ci-C6-alkyl, Ci-C6-haloalkyl, Ci-C6-alkoxy, Ci-C6-haloalkoxy, Ci-C6-alkylthio, Ci-C6-haloalkylthio, Cs-Cs-cycloalkyl, Cs-Cs-halocycloalkyl, C2-C6-alkenyl, C2-C6-haloalkenyl, C2-C6-alkynyl, C2-C6 haloalkynyl, phenyl, optionally substituted with 1 , 2, 3, 4 or 5 identical or different substituents R ¹⁰ , and a 3-, 4-, 5-, 6- or 7- membered saturated, partly saturated or unsaturated aromatic C-bound heterocyclic ring comprising 1 , 2 or 3 heteroatoms as ring members, which are identical or different and selected from oxygen, nitrogen and sulfur, where the heterocyclic ring is optionally substituted with 1 , 2, 3 or 4 identical or different substituents R ¹⁰ , and wherein the nitrogen and/or the sulfur atom(s) of the heterocyclic ring may optionally be oxidized,

or

R ^9a and R ^9b together may form =CR ¹³ R ¹⁴ , =NR ¹⁷ or =NOR ¹⁶ moiety;

R ¹⁰ independently of its occurrence, is selected from the group consisting of halogen, cyano, azido, nitro, SCN, SF ₅ , Ci-Cio-alkyl, Cs-Cs-cycloalkyl, C2-Cio-alkenyl, C2-C10- alkynyl, wherein the carbon atoms of the aforementioned aliphatic and cycloaliphatic radicals may optionally be substituted with 1 , 2, 3, 4 or 5 identical or different radicals R ⁷ ,

Si(R ¹¹ ) ₂ R ¹² , OR ¹⁶ , OS(0) _n R ¹⁶ , -S(0) _n R ¹⁶ , S(0) _n NR ^7a R ^7b , NR ^17a R ^17b , C(=0)R ¹⁵ , C(=S)R ¹⁵ , C(=0)OR ¹⁶ , -C(=NR ⁷ )R ¹⁵ , C(=0)NR ^7a R ^7b , C(=S)NR ^7a R ⁷ ,

phenyl, optionally substituted with 1 , 2, 3, 4 or 5 identical or different radicals selected from OH, halogen, cyano, nitro, Ci-C6-alkyl, Ci-C6-haloalkyl, Ci-C6-alkoxy and Ci-C6-haloalkoxy, and

a 3-, 4-, 5-, 6- or 7- membered saturated, partly saturated or unsaturated aromatic heterocyclic ring comprising 1 , 2 or 3 heteroatoms as ring members, which are identical or different and selected from oxygen, nitrogen and sulfur, where the heterocyclic ring is unsubstituted or may be substituted with 1 , 2, 3, 4 or 5 substituents selected independently from one another from halogen, cyano, NO2, Ci-C6-alkyl, Ci-C6-haloalkyl, Ci-C6-alkoxy and Ci-C6-haloalkoxy, and wherein the nitrogen and/or the sulfur atom(s) of the heterocyclic ring may optionally be oxidized; or

two R ¹⁰ present together on one carbon ring atom of a saturated or partly unsaturated heterocyclic radical may form =0, =CR ¹³ R ¹⁴ , =S, =NR ¹⁷ , =NOR ¹⁶ , =NNR ^17a R ^17b ;

or,

two R ¹⁰ on adjacent carbon ring atoms may also be a bivalent radical selected from CH2CH2CH2CH2, CH=CH-CH=CH, N=CH-CH=CH, CH=N-CH=CH, N=CH-N=CH, OCH2CH2CH2, OCH=CHCH ₂ , CH2OCH2CH2, OCH2CH2O, OCH2OCH2, CH2CH2CH2, CH=CHCH ₂ , CH2CH2O, CH=CHO, CH ₂ OCH ₂ , CH ₂ C(=0)0, C(=0)OCH ₂ , 0(CH ₂ )0, SCH2CH2CH2, SCH=CHCH ₂ , CH ₂ SCH ₂ CH ₂ , SCH ₂ CH ₂ S, SCH ₂ SCH ₂ , CH ₂ CH ₂ S, CH=CHS, CH2SCH2, CH ₂ C(=S)S, C(=S)SCH ₂ , S(CH ₂ )S, CH ₂ CH ₂ NR ¹⁷ , CH ₂ CH=N, CH=CH-NR ¹⁷ , OCH=N, SCH=N and form together with the carbon atoms to which the two R ¹⁰ are bonded to a 5-membered or 6-membered partly saturated or unsaturated, aromatic carbocyclic or heterocyclic ring, wherein the ring may optionally be substituted with one or two substituents selected from =0, OH, CH3,

OCH3, halogen, cyano, halomethyl and halomethoxy;

R ¹¹ , R ¹² independently of their occurrence, are selected from the group consisting of d-Ce-alkyl, Ci-C ₆ -haloalkyl, Ci-C ₆ -alkoxy, Ci-C ₆ -alkoxy-Ci-C ₄ -alkyl, C ₂ -C ₆ - alkenyl, C ₂ -C6-haloalkenyl, C ₂ -C6-alkynyl, C ₂ -C6-haloalkynyl, Cs-Cs-cycloalkyl,

C3-C8-halocycloalkyl, C3-C8-cycloalkyl-Ci-C ₄ -alkyl, C3-Cs-halocycloalkyl-Ci-C ₄ - alkyl, Ci-C6-haloalkoxy-Ci-C ₄ -alkyl, phenyl and benzyl, where the phenyl ring in last two radicals are unsubstituted or substituted with 1 , 2, 3, 4 or 5 identical or different radicals selected from halogen, OH, cyano, N0 ₂ , Ci-C6-alkyl,

Ci-C6-haloalkyl, Ci-C6-alkoxy and Ci-C6-haloalkoxy;

R ¹³ , R ¹⁴ independently of their occurrence, are selected from the group consisting of hydrogen, halogen, CN, Ci-C6-alkyl, C3-C6-cycloalkyl, Ci-C ₄ -alkoxy-Ci-C ₄ - alkyl, phenyl and benzyl;

R ¹⁵ independently of its occurrence, is selected from the group consisting of hydrogen, Ci-C6-alkyl, C ₂ -C6-alkenyl, C ₂ -C6-alkynyl, Cs-Cs-cycloalkyl, C3-Cs-cycloalkyl-Ci-C ₄ - alkyl, wherein the five last mentioned aliphatic and cycloaliphatic radicals may be unsubstituted, partially or fully halogenated and/or oxygenated and/or may carry 1 or 2 radicals selected from Ci-C ₄ -alkoxy;

phenyl, benzyl and pyridyl, wherein the last three radicals may be unsubstituted, partially or fully halogenated and/or may carry 1 , 2 or 3 substituents selected from Ci-C6-alkyl, Ci-C6-haloalkyl, Ci-C6-alkoxy, C1-C6 haloalkoxy, (Ci-C6-alkoxy)carbonyl, (Ci-C6-alkyl)amino or di-(Ci-C6-alkyl)amino;

R ¹⁶ independently of its occurrence, is selected from the group consisting of hydrogen, Ci-C6-alkyl, C ₂ -C6-alkenyl, C ₂ -C6-alkynyl, Cs-Cs-cycloalkyl, C3-Cs-cycloalkyl-Ci-C ₄ - alkyl, wherein the five last mentioned aliphatic and cycloaliphatic radicals may be unsubstituted, partially or fully halogenated and/or oxygenated and/or may carry 1 or 2 radicals selected from Ci-C ₄ -alkoxy, phenyl, benzyl and pyridyl, wherein the last three radicals may be unsubstituted, partially or fully halogenated and/or may carry 1 , 2 or 3 substituents selected from Ci-C6-alkyl, Ci-C6-haloalkyl, Ci-C6-alkoxy, C1-C6 haloalkoxy, (Ci-C6-alkoxy)carbonyl, (Ci-C6-alkyl)amino or di-(Ci-C6-alkyl)amino;

R ¹⁷ independently of its occurrence, is selected from the group consisting of hydrogen, trimethylsilyl, triethylsilyl, fer/butyldimethylsilyl,

Ci-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, Cs-Cs-cycloalkyl, C3-Cs-cycloalkyl-Ci-C4- alkyl, Ci-C6-alkoxy, C2-C6-alkenyloxy, C2-C6-alkynyloxy, C3-Cs-cycloalkoxy, C3-C8- cycloalkyl-Ci-C4-alkoxy, Ci-C6-alkylthio, wherein the 1 1 last mentioned aliphatic and cycloaliphatic radicals may be unsubstituted, partially or fully halogenated and/or oxygenated and/or may carry 1 or 2 radicals selected from Ci-C4-alkoxy,

phenyl, benzyl, pyridyl, phenoxy, benzyloxy, pyridyloxy, wherein the six last mentioned radicals may be unsubstituted, partially or fully halogenated and/or carry 1 , 2 or 3 substituents selected from halogen, Ci-C6-alkyl, Ci-C6-haloalkyl, C1-C6- alkoxy, C1-C6 haloalkoxy and (Ci-C6-alkoxy)carbonyl,

R ^17a , R ^17b are each independently from one another selected from the group consisting of hydrogen, Ci-C6-alkoxy, Ci-C6-haloalkoxy, Ci-C6-alkylthio, C1-C6- alkylsulfinyl, Ci-C6-alkylsulfonyl, Ci-C6-haloalkylthio, trimethylsilyl, triethylsilyl, ferfbutyldimethylsilyl,

Ci-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, Cs-Cs-cycloalkyl, wherein the four last mentioned aliphatic and cyclo-aliphatic radicals may be unsubstituted, partially or fully halogenated and/or oxygenated and/or may carry 1 or 2 radicals selected from Ci-C4-alkoxy,

phenyl, benzyl, pyridyl, phenoxy, wherein the four last mentioned radicals may be unsubstituted, partially or fully halogenated and/or may carry 1 , 2 or 3 substituents selected from Ci-C6-alkyl, Ci-C6-haloalkyl, Ci-C6-alkoxy, C1-C6 haloalkoxy and (Ci-C6-alkoxy)carbonyl,

or,

R ^17a and R ^17b may together be a C2-C6 alkylene chain forming a 3- to 7- membered saturated, partly saturated or unsaturated ring together with the nitrogen atom R ^17a and R ^17b are bonded to, wherein the alkylene chain may contain 1 or 2 heteroatoms selected, independently of each other, from oxygen, sulfur or nitrogen, and may optionally be substituted with halogen, Ci-C4-haloalkyl, Ci-C4-alkoxy or Ci-C4-haloalkoxy, and wherein the nitrogen and/or the sulfur atom(s) of the heterocyclic ring may optionally be oxidized; or

R ^17a and R ^17b together may form =CR ¹³ R ¹⁴ , =NR ¹⁷ or =NOR ¹⁶ moiety;

R ^17c independently of its occurrence, is selected from the group consisting of hydrogen, CN, d-Ce-alkyl, C ₂ -C ₆ -alkenyl, C ₂ -C ₆ -alkynyl, C ₃ -C ₈ -cycloalkyl, C ₃ -C ₈ -cycloalkyl-Ci- C4-alkyl, wherein the five last mentioned aliphatic and cycloaliphatic radicals may be unsubstituted, partially or fully halogenated and/or oxygenated and/or may carry 1 or 2 radicals selected from Ci-C4-alkoxy,

phenyl, benzyl and pyridyl, wherein the last three radicals may be unsubstituted, partially or fully halogenated and/or may carry 1 , 2 or 3 substituents selected from Ci-C6-alkyl, Ci-C6-haloalkyl, Ci-C6-alkoxy, C1-C6 haloalkoxy, (Ci-C6-alkoxy)carbonyl, (Ci-C6-alkyl)amino or di-(Ci-C6-alkyl)amino; the stereoisomers, the tautomers and the salts thereof.

The present invention relates, in particular, to compounds of the formula (I), to the stereoisomers, the tautomers and the salts thereof, where Het is not tetrahydrofuran-3-yl, optionally substituted by k identical or different substituents R ⁶ , if R ³ and R ⁵ together form a bivalent radical, selected from the group consisting of C2-C6-alkanediyl and C2-C6-alkenediyl, wherein the carbon atom in the two aforementioned radicals are unsubstituted or may carry 1 , 2, 3 or 4 radicals R ^7c .

Moreover, the present invention relates to and includes the following embodiments:

agricultural and veterinary compositions comprising an amount of at least one compound of the formula (I) or a stereoisomer, tautomer or salt thereof;

the use of the compounds of formula (I), the stereoisomers, the tautomers or the salts thereof for combating invertebrate pests;

the use of the compounds of formula (I), the stereoisomers, the tautomers or the salts thereof for protecting growing plants from attack or infestation by invertebrate pests;

the use of the compounds of formula (I), the stereoisomers, the tautomers or the salts, thereof for protecting plant proparagation material, especially seeds, from soil insects; the use of the compounds of formula (I), the stereoisomers, the tautomers or the salts thereof for protecting the seedlings roots and shoots of plants from soil and foliar insects; a method for combating or controlling invertebrate pests, which method comprises contacting said pest or its food supply, habitat or breeding grounds with a pesticidally effective amount of at least one compound of the formula (I) or a stereoisomer, a tautomer or salt thereof;

a method for protecting growing plants from attack or infestation by invertebrate pests, which method comprises contacting a plant, or soil or water in which the plant is growing, with a pesticidally effective amount of at least one compound of the formula (I) or a stereoisomer, a tautomer or salt thereof, in particular a method protecting crop plants from attack or infestation by animal pests, which comprises contacting the crop plants with a pesticidally effective amount of at least one compound of the formula (I) or stereoisomer, a tautomer or salt thereof;

a method for the protection of plant propagation, especially seeds, from soil insects and of the seedlings' roots and shoots from soil and foliar insects comprising contacting the seeds before sowing and/or after pregermination with at least one compound of the formula (I) or stereoisomer, a tautomer or salt thereof;

seeds comprising a compound of the formula (I) or an enantiomer, diastereomer or salt thereof;

the use of compounds of formula (I), the stereoisomers, the tautomers or the salts, in particular the veterinary acceptable salts, thereof for combating parasites in and on animals, in particular for the use in the treatment of animals infested or infected by parasites, for preventing animals of getting infected or infested by parasites or for protecting animals against infestation or infection by parasites;

a method for treating animals infested or infected by parasites or preventing animals of getting infected or infested by parasites or protecting animals against infestation or infection by parasites which comprises administering or applying to the animals a parasiticidally effective amount of a compound of formula (I) or the stereoisomers and/or salts, in particular veterinary acceptable salts, thereof;

a process for the preparation of a veterinary composition for treating, controlling, preventing or protecting animals against infestation or infection by parasites which comprises formulating a compound of formula (I) or a stereoisomer, tautomer and/or veterinary acceptable salt thereof with a carrier composition suitable for veterinary use; the use of a compound of formula (I) or the stereoisomers, tautomers and/or veterinary acceptable salt thereof for the preparation of a medicament for treating, controlling, preventing or protecting animals against infestation or infection by parasites. The present invention also relates to plant propagation materials, in particular as mentioned above to seeds, containing at least one compound of formula (I), a stereoisomer, a tautomer and/or an agriculturally acceptable salt thereof. Detailed Description of Invention

The present invention relates to every possible stereoisomer of the compounds of formula (I), i.e. to single enantiomers, diastereomers and E/Z-isomers as well as to mixtures thereof and also to the salts thereof. The present invention relates to each isomer alone, or mixtures or combinations of the isomers in any proportion to each other. In particular the radicals Y and

R ³ may be cis or trans with respect to the C=N bond. Suitable compounds of the formula (I) also include all possible geometrical stereoisomers (cis/trans isomers) and mixtures thereof.

Depending on the substitution pattern, the compounds of the formula (I) may have one or more centers of chirality, in which case they are present as mixtures of enantiomers or diastereomers. One center of chirality is the carbon ring atom carrying radical R ¹ . The invention provides both the pure enantiomers or diastereomers and their mixtures and the use according to the invention of the pure enantiomers or diastereomers of the compound I or its mixtures.

The present invention also relates to potential tautomers of the compounds of formula (I) and also to the salts of such tautomers. The present invention relates to the tautomer as such as well as to mixtures or combinations of the tautomers in any proportion to each other. The term "tautomers" encompasses isomers, which are derived from the compounds of formula (I) by the shift of an H-atom involving at least one H-atom located at a nitrogen, oxygen or sulphur atom. Examples of tautomeric forms are keto-enol forms, imine-enamine forms, urea-isourea forms, thiourea-isothiourea forms, (thio)amide-(thio)imidate forms etc.

The compounds of the present invention, i.e. the compounds of formula (I), their stereoisomers, their tautomers as well as their salts, in particular their agriculturally acceptable salts and their veterinarily acceptable salts, may be amorphous or may exist in one ore more different crystalline states (polymorphs) or modifications which may have a different

macroscopic properties such as stability or show different biological properties such as activities. The present invention includes both amorphous and crystalline compounds of the formula (I), mixtures of different crystalline states or modifications of the respective

stereoisomers or tautomers, as well as amorphous or crystalline salts thereof.

Salts of the compounds of the formula (I) are preferably agriculturally salts as well as veterinarily acceptable salts. They can be formed in a customary method, e.g. by reacting the compound with an acid of the anion in question if the compound of formula (I) has a basic functionality or by reacting an acidic compound of formula (I) with a suitable base.

Suitable agriculturally or veterinary useful salts are especially the salts of those cations or anions, in particular the acid addition salts of those acids, whose cations and anions, respectively, do not have any adverse effect on the action of the compounds according to the present invention. Suitable cations are in particular the ions of the alkali metals, preferably lithium, sodium and potassium, of the alkaline earth metals, preferably calcium, magnesium and barium, and of the transition metals, preferably manganese, copper, zinc and iron, and also ammonium (NhV) and substituted ammonium in which one to four of the hydrogen atoms are replaced by Ci-C4-alkyl, Ci-C4-hydroxyalkyl, Ci-C4-alkoxy, Ci-C4-alkoxy-Ci-C4-alkyl, hydroxy-Ci- C4-alkoxy-Ci-C4-alkyl, phenyl or benzyl. Examples of substituted ammonium ions comprise methylammonium, isopropylammonium, dimethylammonium, diisopropylammonium, trimethylammonium, tetramethylammonium, tetraethylammonium, tetrabutylammonium, 2- hydroxyethylammonium, 2-(2-hydroxyethoxy)ethyl-ammonium, bis(2-hydroxyethyl)ammonium, benzyltrimethylammonium and benzyltriethylammonium, furthermore phosphonium ions, sulfonium ions, preferably tri(Ci-C4-alkyl)sulfonium, and sulfoxonium ions, preferably tri(Ci-C4- alkyl)sulfoxonium.

Anions of useful acid addition salts are primarily chloride, bromide, fluoride, hydrogen sulfate, sulfate, dihydrogen phosphate, hydrogen phosphate, phosphate, nitrate, hydrogen carbonate, carbonate, hexafluorosilicate, hexafluorophosphate, benzoate, and the anions of Ci- C4-alkanoic acids, preferably formate, acetate, propionate and butyrate. They can be formed by reacting the compounds of the formulae I with an acid of the corresponding anion, preferably of hydrochloric acid, hydrobromic acid, sulfuric acid, phosphoric acid or nitric acid.

The organic moieties mentioned in the above definitions of the variables are - like the term halogen - collective terms for individual listings of the individual group members. The prefix Cn-Cm indicates in each case the possible number of carbon atoms in the group.

"Halogen" will be taken to mean fluoro, chloro, bromo and iodo.

The term "partially or fully halogenated" will be taken to mean that 1 or more, e.g. 1 , 2, 3, 4 or 5 or all of the hydrogen atoms of a given radical have been replaced by a halogen atom, in particular by fluorine or chlorine. For example, partially or fully halogenated alkyl is also termed haloalkyl, partially or fully halogenated cycloalkyl is also termed halocycloalkyl, partially or fully halogenated alkylenyl is also termed haloalkenyl, partially or fully halogenated alkylynyl is also termed haloalkynyl, partially or fully halogenated alkoxy is also termed haloalkoxy, partially or fully halogenated alkylthio is also termed haloalkthio, partially or fully halogenated alkylsulfinyl is also termed haloalkylsulfinyl, partially or fully halogenated alkylsulfonyl is also termed haloalsulfonyl, partially or fully halogenated cycloalkylalkyl is also termed halocycloalkylalkyl.

The term "C _n -C _m -alkyl" as used herein, and also in C _n -C _m -alkylamino, di-C _n -C _m -alkylamino, Cn-Cm-alkylaminocarbonyl, di-(C _n -C _m -alkylamino)carbonyl, C _n -C _m -alkylthio, C _n -C _m -alkylsulfinyl and C _n -C _m -alkylsulfonyl, refers to a branched or unbranched saturated hydrocarbon group having n to m, e.g. 1 to 10 carbon atoms, preferably 1 to 6 carbon atoms, for example methyl, ethyl, propyl, 1 -methylethyl, butyl, 1 -methylpropyl, 2-methylpropyl, 1 ,1 -dimethylethyl, pentyl, 1 - methylbutyl, 2-methylbutyl, 3-methylbutyl, 2,2-dimethylpropyl, 1 -ethylpropyl, hexyl, 1 ,1 - dimethylpropyl, 1 ,2-dimethylpropyl, 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, 1 -ethyl-2-methylpropyl, heptyl, octyl, 2-ethylhexyl, nonyl and decyl and their isomers. Ci-C4-alkyl means for example methyl, ethyl, propyl, 1 -methylethyl, butyl, 1 -methylpropyl, 2-methylpropyl or 1 ,1 -dimethylethyl.

The term "C _n -C _m -alkanediyl" as used herein, refers to a linear or branched saturated bivalent hydrocarbon group having n to m, e.g. 1 to 6 carbon atoms, preferably 1 to 4 carbon atoms, for example methylen, ethane-1 ,1 -diyl, ethane-1 ,2-diyl, propane-1 ,1 -diyl, propane-1 ,2- diyl, propane-1 ,3-diyl, propane-2,2-diyl, butane-1 ,1 -diyl, butane-1 ,2-diyl, butane-2,3-diyl, butane-2,2-diyl, butane-1 ,3-diyl, butane-1 ,4-diyl, pentane-1 , 1 -diyl, pentane-2,2-diyl, pentane- 3,3-diyl, pentane-1 ,2-diyl, pentane-1 ,3-diyl, pentane-1 ,4-diyl, pentane-1 ,5-diyl, pentane-2,3-diyl, pentane-2,4-diyl, 2-methylbutane-1 ,4-diyl, 2,2-dimethylpropane-1 ,3-diyl, hexane-1 ,6-diyl, hexane-1 ,5-diyl or 2,5-hexane-2,5-diyl. The term "linear Ci-C6-alkanediyl" refers to a linear saturated bivalent hydrocarbon group having 1 to 6 carbon atoms, preferably 1 to 4 carbon atoms, for example methylene, ethane-1 ,2-diyl, propane-1 ,3-diyl, butane-1 ,4-diyl, pentane-1 ,5- diyl and hexane-1 ,6-diyl.

The term "C _n -C _m -haloalkyl" as used herein, and also in C _n -C _m -haloalkylthio (= C _n -C _m - haloalkylsulfenyl = C _n -C _m -haloalkylsulfanyl), C _n -C _m -haloalkylsulfinyl and C _n -C _m -haloalkylsulfonyl, refers to a straight-chain or branched alkyl group having n to m carbon atoms, e.g. 1 to 10 in particular 1 to 6 carbon atoms (as mentioned above), where some or all of the hydrogen atoms in these groups may be replaced by halogen atoms as mentioned above, for example C1-C4- haloalkyl, such as chloromethyl, bromomethyl, dichloromethyl, trichloromethyl, fluoromethyl, difluoromethyl, trifluoromethyl, chlorofluoromethyl, dichlorofluoromethyl, chlorodifluoromethyl, 1 - chloroethyl, 1 -bromoethyl, 1 -fluoroethyl, 2-fluoroethyl, 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, pentafluoroethyl, 2,2-difluoropropyl, 3,3,3-trifluoropropyl, 2,2,3,3,3-pentafluoropropyl, 2-fluoro-1 - methylethyl, 2,2-difluoro-1 -methylethyl, 2,2,2-trifluoro-1 -methylethyl, 2,2,2-trifluoro-1 - (trifluoromethyl)ethyl, 1 ,2,2,2-tetrafluoro-1 -(trifluoromethyl)ethyl and the like. The term C1-C10- haloalkyl in particular comprises Ci-C2-fluoroalkyl, which is synonym with methyl or ethyl, wherein 1 , 2, 3, 4 or 5 hydrogen atoms are substituted by fluorine atoms, such as fluoromethyl, difluoromethyl, trifluoromethyl, 1 -fluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl and pentafluoromethyl. "Halomethyl" is methyl in which 1 , 2 or 3 of the hydrogen atoms are replaced by halogen atoms. Examples are bromomethyl, chloromethyl, fluoromethyl, dichloromethyl, trichloromethyl, difluoromethyl, trifluoromethyl, chlorofluoromethyl,

dichlorofluoromethyl, chlorodifluoromethyl and the like.

Similarly, "C _n -C _m -alkoxy", "C _n -C _m -alkylthio", or "C _n -C _m -alkylsulfenyl", respectively, "C _n -C _m - alkylsulfinyl" or "C _n -C _m -alkylsulfonyl" refer to straight-chain or branched alkyl groups having n to m carbon atoms, e.g. 1 to 10, in particular 1 to 6 or 1 to 4 carbon atoms (as mentioned above) bonded through O, S, S(=0) or S(=0)2 linkages, respectively, at any bond in the alkyl group. Accordingly, the terms "C _n -C _m -haloalkoxy", "C _n -C _m -haloalkylthio" or "Cn-Cm-alkylsulfenyl", respectively, "C _n -C _m -haloalkylsulfinyl" or "C _n -C _m -haloalkylsulfonyl", refer to straight-chain or branched alkyl groups having n to m carbon atoms, e.g. 1 to 10, in particular 1 to 6 or 1 to 4 carbon atoms (as mentioned above) bonded through O, S, S(=0) or S(=0)2 linkages, respectively, at any bond in the haloalkyl group, where some or all of the hydrogen atoms in these groups may be replaced by halogen atoms as mentioned above.

The term "C _n -C _m -alkoxy" is a C _n -C _m -alkyl group, as defined above, attached via an oxygen atom. Ci-C2-Alkoxy is methoxy or ethoxy. Ci-C4-Alkoxy is, for example, methoxy, ethoxy, n- propoxy, 1 -methylethoxy (isopropoxy), butoxy, 1 -methylpropoxy (sec-butoxy), 2-methylpropoxy (isobutoxy) or 1 ,1 -dimethylethoxy (tert-butoxy). Ci-C6-Alkoxy includes the meanings given for Ci-C4-alkoxy and also includes, for example, pentoxy, 1 -methylbutoxy, 2-methylbutoxy, 3- methylbutoxy, 1 ,1 -dimethylpropoxy, 1 ,2-dimethylpropoxy, 2,2-dimethylpropoxy, 1 -ethylpropoxy, hexoxy, 1 -methylpentoxy, 2-methylpentoxy, 3-methylpentoxy, 4-methylpentoxy, 1 ,1 - dimethylbutoxy, 1 ,2-dimethylbutoxy, 1 ,3-dimethylbutoxy, 2,2-dimethylbutoxy, 2,3- dimethylbutoxy, 3,3-dimethylbutoxy, 1 -ethylbutoxy, 2-ethyl butoxy, 1 ,1 ,2-trimethylpropoxy, 1 ,2,2- trimethylpropoxy, 1 -ethyl-1 -methylpropoxy or 1 -ethyl-2-methylpropoxy. Ci-Cs-Alkoxy includes the meanings given for Ci-C6-alkoxy and also includes, for example, heptyloxy, octyloxy, 2- ethylhexyloxy and positional isomers thereof. Ci-Cio-Alkoxy includes the meanings given for Ci- Ce-alkoxy and also includes, for example, nonyloxy, decyloxy and positional isomers thereof.

The term "C _n -C _m -alkylthio" (also referred to as "C _n -C _m -alkylsulfanyl) is a C _n -C _m -alkyl group, as defined above, attached via a sulfur atom. Ci-C2-Alkylthio is methylthio or ethylthio. C1-C4- Alkylthio is, for example, methylthio, ethylthio, n-propylthio, 1 -methylethylthio (isopropylthio), butylthio, 1 -methylpropylthio (sec-butylthio), 2-methylpropylthio (isobutylthio) or 1 ,1 - dimethylethylthio (tert-butylthio). Ci-C6-Alkylthio includes the meanings given for Ci-C4-alkylthio and also includes, for example, pentylthio, 1 -methylbutylthio, 2-methylbutylthio, 3- methylbutylthio, 1 ,1 -dimethylpropylthio, 1 ,2-dimethylpropylthio, 2,2-dimethylpropylthio, 1 - ethylpropylthio, hexylthio, 1 -methylpentylthio, 2-methylpentylthio, 3-methylpentylthio, 4- methylpentylthio, 1 ,1 -dimethylbutylthio, 1 ,2-dimethylbutylthio, 1 ,3-dimethylbutylthio, 2,2- dimethylbutylthio, 2,3-dimethylbutylthio, 3,3-dimethylbutylthio, 1 -ethylbutylthio, 2-ethylbutylthio, 1 ,1 ,2-trimethylpropylthio, 1 ,2,2-trimethylpropylthio, 1 -ethyl-1 -methylpropylthio or 1 -ethyl-2- methylpropylthio. Ci-Cs-Alkylthio includes the meanings given for Ci-C6-alkylthio and also includes, for example, heptylthio, octylthio, 2-ethylhexylthio and positional isomers thereof. Ci- Cio-Alkylthio includes the meanings given for Ci-Cs-alkylthio and also includes, for example, nonylthio, decylthio and positional isomers thereof.

The term "C _n -C _m -a I kylsu If i nyl" is a C _n -C _m -alkyl group, as defined above, attached via a S(=0) group. The term "C _n -C _m -alkylsulfonyl" is a C _n -C _m -alkyl group, as defined above, attached via a S(=0)2 group.

The term "C _n -C _m -haloalkyloxy" is a C _n -C _m -haloalkyl group, as defined above, attached via an oxygen atom. Examples include Ci-C2-haloalkoxy, such as chloromethoxy, bromomethoxy, dichloromethoxy, trichloromethoxy, fluoromethoxy, difluoromethoxy, trifluoromethoxy, chlorofluoromethoxy, dichlorofluoromethoxy, chlorodifluoromethoxy, 1 -chloroethoxy, 1 - bromoethoxy, 1 -fluoroethoxy, 2-fluoroethoxy, 2,2-difluoroethoxy, 2,2,2-trifluoroethoxy, 2-chloro- 2-fluoroethoxy, 2-chloro-2,2-difluoroethoxy, 2,2-dichloro-2-fluoroethoxy, 2,2,2-trichloroethoxy and pentafluoroethoxy.

The term "C _n -C _m -haloalkylthio" is a C _n -C _m -haloalkyl group, as defined above, attached via a sulfur atom. Examples include Ci-C2-haloalkylthio, such as chloromethylthio,

bromomethylthio, dichloromethylthio, trichloromethylthio, fluoromethylthio, difluoromethylthio, trifluoromethylthio, chlorofluoromethylthio, dichlorofluoromethylthio, chlorodifluoromethylthio, 1 - chloroethylthio, 1 -bromoethylthio, 1 -fluoroethylthio, 2-fluoroethylthio, 2,2-difluoroethylthio, 2,2,2- trifluoroethylthio, 2-chloro-2-fluoroethylthio, 2-chloro-2,2-difluoroethylthio, 2,2-dichloro-2- fluoroethylthio, 2,2,2-trichloroethylthio and pentafluoroethylthio and the like.

Similarly the terms Ci-C2-fluoroalkoxy and Ci-C2-fluoroalkylthio refer to Ci-C2-fluoroalkyl which is bound to the remainder of the molecule via an oxygen atom or a sulfur atom, respectively.

The term "C _n -C _m -haloalkylsulfinyl" is a C _n -C _m -haloalkyl group, as defined above, attached via a S(=0) group. The term "Ci-C _m -haloalkylsulfonyl" is a Ci-C _m -haloalkyl group, as defined above, attached via a S(=0)2 group. The term "C2-C _m -alkenyl" as used herein denotes a linear or branched ethylenically unsaturated hydrocarbon group having 2 to m, e.g.2 to 10 or 2 to 6 carbon atoms and a C=C- double bond in any position, such as ethenyl, 1-propenyl, 2-propenyl, 1-methyl-ethenyl, 1- butenyl, 2-butenyl, 3-butenyl, 1-methyl-1-propenyl, 2-methyl-1-propenyl, 1-methyl-2-propenyl, 2- methyl-2-propenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, 1-methyl-1-butenyl, 2-methyl- 1-butenyl, 3-methyl-1-butenyl, 1-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl-2-butenyl, 1- methyl-3-butenyl, 2-methyl-3-butenyl, 3-methyl-3-butenyl, 1,1-dimethyl-2-propenyl, 1,2-dimethyl-

1- propenyl, 1,2-dimethyl-2-propenyl, 1-ethyl-1-propenyl, 1-ethyl-2-propenyl, 1-hexenyl, 2- hexenyl, 3-hexenyl, 4-hexenyl, 5-hexenyl, 1-methyl-1-pentenyl, 2-methyl-1-pentenyl, 3-methyl- 1-pentenyl, 4-methyl-1-pentenyl, 1-methyl-2-pentenyl, 2-methyl-2-pentenyl, 3-methyl-2- pentenyl, 4-methyl-2-pentenyl, 1-methyl-3-pentenyl, 2-methyl-3-pentenyl, 3-methyl-3-pentenyl, 4-methyl-3-pentenyl, 1-methyl-4-pentenyl, 2-methyl-4-pentenyl, 3-methyl-4-pentenyl, 4-methyl- 4-pentenyl, 1,1-dimethyl-2-butenyl, 1,1-dimethyl-3-butenyl, 1,2-dimethyl-1-butenyl, 1,2-dimethyl-

2- butenyl, 1,2-dimethyl-3-butenyl, 1,3-dimethyl-1-butenyl, 1,3-dimethyl-2-butenyl, 1,3-dimethyl- 3-butenyl, 2,2-dimethyl-3-butenyl, 2,3-dimethyl-1 -butenyl, 2,3-dimethyl-2-butenyl, 2,3-dimethyl-

3- butenyl, 3, 3-dimethyl-1 -butenyl, 3,3-dimethyl-2-butenyl, 1 -ethyl-1 -butenyl, 1-ethyl-2-butenyl, 1- ethyl-3-butenyl, 2-ethyl-1 -butenyl, 2-ethyl-2-butenyl, 2-ethyl-3-butenyl, 1,1,2-trimethyl-2- propenyl, 1 -ethyl-1 -methyl-2-propenyl, 1-ethyl-2-methyl-1-propenyl and 1-ethyl-2-methyl-2- propenyl.

The term "C2-C _m -haloalkenyl" as used herein, which is also expressed as "C2-C _m -alkenyl which is partially or fully halogenated", refers to C2-C _m -alkenyl, where some or all of the hydrogen atoms in these groups are replaced by halogen atoms as mentioned above, in particular fluorine, chlorine and bromine, for example 1-fluoroethenyl, 2-fluoroethenyl, 2,2- difluoroethenyl, 1,2,2-trifluoroethenyl, 1-fluoro-2-propenyl, 2-fluoro-2-propenyl, 3-fluoro-2- propenyl, 1-fluoro-1-propenyl, 1,2-difluoro-1-propenyl, 3,3-difluoropropen-2-yl, 1-chloroethenyl, 2-chloroethenyl, 2,2,-dichloroethenyl, 1-chloro-2-propenyl, and the like.

The term "C2-C _m -alkenediyl" as used herein, refers to linear or branched mono- unsaturated bivalent hydrocarbon group having 2 to m, e.g.2 to 6 carbon atoms, preferably 2 to 4 carbon atoms, for example ethene-1 ,1-diyl, ethene-1,2-diyl, prop-1-ene-1 ,1-diyl, prop-1-ene- 1,2-diyl, prop-2-ene-1,1-diyl, prop-2-ene-1,2-diyl, propene-1,3-diyl, but-1 -ene-1 ,1 -diyl, but-1- ene-1,2-diyl, but-1 -ene-1 ,3-diyl, but-2-ene-1 ,1-diyl, but-2-ene-1,2-diyl, but-3-ene-1,1-diyl, but-3- ene-1,2-diyl, but-2-ene-1,2-diyl, but-2-ene-1 ,3-diyl, but-1 -ene-1 ,4-diyl, but-2-ene-1,4-diyl, pent- 1 -ene-1 ,5-diyl, pent-2 -ene-1 ,5-diyl, hex-1 -ene-1 ,6-diyl, hex-2-ene-1 ,6-diyl or hex-3-ene-1,6-diyl. The term "C2-C _m -alkynyl" as used herein refers to linear or branched unsaturated hydrocarbon group having 2 to m, e.g. 2 to 10 or 2 to 6 carbon atoms and containing at least one C-C-triple bond, such as ethynyl, propynyl, 1 -butynyl, 2-butynyl, and the like.

The term "C2-C _m -haloalkynyl" as used herein, which is also expressed as "C2-C _m -alkynyl which is partially or fully halogenated", refers to C2-C _m -alkynyl, where some or all of the hydrogen atoms in these groups are replaced by halogen atoms as mentioned above, in particular fluorine, chlorine and bromine. Examples of C2-C _m -haloalkynyl include 1 -fluoro-2- propenyl, 2-fluoro-2-propenyl, 3-fluoro-2-propenyl, 1 -fluoro-2-propynyl and 1 ,1 -difluoro-2- propenyl, and the like.

The term "C2-C _m -alkynediyl" as used herein, refers to linear or branched mono- unsaturated bivalent hydrocarbon group having a C-C-triple bond and 2 to m, e.g. 2 to 6 carbon atoms, preferably 2 to 4 carbon atoms, for example ethyne-1 ,2-diyl, prop-2-yne-1 ,1 -diyl, prop-1 - yne-1 ,3-diyl, but-2-yne-1 ,1 -diyl, but-1 -yne-1 ,3-diyl, but-1 -yne-1 ,4-diyl, but-2-yne-1 ,4-diyl, pent-1 - yne-1 ,5-diyl, pent-2 -yne-1 ,5-diyl, hex-1 -yne-1 ,6-diyl, hex-2 -yne-1 ,6-diyl or hex-3-yne-1 ,6-diyl.

The term "C3-C _m -cycloalkyl" as used herein refers to monocyclic and polycyclic 3- to m- membered saturated cycloaliphatic radicals, e.g. cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, cyclodecyl, bicyclo[2.2.1]heptyl, bicyclo[3.1 .1 ]heptyl, bicyclo[2.2.2]octyl and bicyclo[3.2.1]octyl. Preferably, the term cycloalkyl denotes a monocyclic saturated hydrocarbon radical.

The term "C3-C _m -cycloalkanediyl" as used herein refers to monocyclic and polycyclic 3- to m-membered saturated bivalent cycloaliphatic radicals, e.g. cyclopropane-1 ,1 -diyl, cis- or trans- cyclopropane-1 ,2-diyl, cyclobutane-1 ,1 -diyl, cis- or trans-cyclobutane-1 ,2-diyl, cyclopentane-1 ,1 - diyl, cis- or trans-cyclopentane-1 ,2-diyl, cis- or trans-cyclopentane-1 ,3-diyl, cyclohexane-1 ,1 - diyl, cis- or trans-cyclohexane-1 ,2-diyl and cis- or trans-cyclohexane-1 ,3-diyl and cis- or trans- cyclohexane-1 ,4-diyl. Preferably, the term cycloalkanediyl denotes a monocyclic saturated bivalent hydrocarbon radical.

The term "C3-C _m -cycloalkenyl" as used herein refers to monocyclic and polycyclic 3- to m- membered monounsaturated cycloaliphatic radicals, e.g. 1 -cyclopropenyl, 3-cyclopropenyl, 1 - cyclobutenyl, 3-cyclobutenyl, cyclopentenyl, 3-cyclopentenyl, 1 -cyclohexenyl, 3-cyclohexenyl, or 4-cyclohexenyl. Preferably, the term cycloalkenyl denotes a monocyclic mono-unsaturated hydrocarbon radical.

The term "C3-C _m -cycloalkenediyl" as used herein refers to a monocyclic and polycyclic 3- to m-membered mono-unsaturated bivalent cycloaliphatic radicals, e.g. cyclobut-2-ene-1 ,1 -diyl, cyclobutene-1 ,2-diyl, cyclobut-3-ene-1 ,2-diyl, cyclopent-2-ene-1 ,1 -diyl, cis- or trans-cyclopent-3- ene-1 ,2-diyl, cyclopent-3-ene-1 ,3-diyl, cyclohex-2-ene-1 ,1 -diyl, cyclohex-3-ene-1 ,1 -diyl, cis- or trans-cyclohex-3-ene-1 ,2-diyl and cis- or trans-cyclohex-4-ene-1 ,3-diyl and cis- or trans- cyclohex-2-ene-1 ,4-diyl. Preferably, the term cycloalkenediyl denotes a monocyclic mono- unsaturated bivalent hydrocarbon radical.

The term "C3-C _m -halocycloalkyl" as used herein, which is also expressed as "cycloalkyl which is partially or fully halogenated", refers C3-C _m -cycloalkyl as mentioned above, in which some or all of the hydrogen atoms are replaced by halogen atoms as mentioned above, in particular fluorine, chlorine and bromine. Examples of C3-C _m -halocycloalkyl include 1 - fluorocyclopropyl, 2-fluorocyclopropyl, 2,2-difluorocyclopropyl, 1 -chlorocyclcopropyl, 2- chlorocyclopropyl, 2,2-dichlorocyclopropyl, 2,3-difluorocyclopropyl, 1 -fluorocycobutyl etc.

The term "C3-C _m -cycloalkyl-Ci-C4-alkyl" refers to a C3-C _m -cycloalkyl group as defined above, which is bound to the remainder of the molecule via a Ci-C4-alkyl group, as defined above. Examples for C3-C _m -cycloalkyl-Ci-C4-alkyl are cyclopropyl methyl, cyclopropylethyl, cyclopropylpropyl, cyclobutyl methyl, cyclobutylethyl, cyclobutylpropyl, cyclopentylmethyl, cyclopentylethyl, cyclopentylpropyl, cyclohexylmethyl, cyclohexylethyl and cyclohexylpropyl.

The term "C3-C _m -halocycloalkyl-Ci-C4-alkyl" refers to a C3-C _m -halocycloalkyl group as defined above which is bound to the remainder of the molecule via a Ci-C4-alkyl group, as defined above.

The term "Ci-C4-alkoxy-Ci-C4-alkyl" as used herein refers to alkyl having 1 to 4 carbon atoms, e.g. like specific examples mentioned above, wherein one hydrogen atom of the alkyl radical is replaced by an Ci-C4-alkoxy group. Examples are methoxymethyl, ethoxymethyl, propoxymethyl, isopropoxymethyl, n-butoxymethyl, sec-butoxymethyl, isobutoxymethyl, tert- butoxymethyl, 1 -methoxyethyl, 1 -ethoxyethyl, 1 -propoxyethyl, 1 -isopropoxyethyl, 1 -n- butoxyethyl, 1 -sec-butoxyethyl, 1 -isobutoxyethyl, 1 -tert-butoxyethyl, 2-methoxyethyl, 2- ethoxyethyl, 2-propoxyethyl, 2-isopropoxyethyl, 2-n-butoxyethyl, 2-sec-butoxyethyl, 2- isobutoxyethyl, 2-tert-butoxyethyl, 1 -methoxypropyl, 1 -ethoxypropyl, 1 -propoxypropyl, 1 - isopropoxypropyl, 1 -n-butoxypropyl, 1 -sec-butoxypropyl, 1 -isobutoxypropyl, 1 -tert-butoxypropyl, 2-methoxypropyl, 2-ethoxypropyl, 2-propoxypropyl, 2-isopropoxypropyl, 2-n-butoxypropyl, 2- sec-butoxypropyl, 2-isobutoxypropyl, 2-tert-butoxypropyl, 3-methoxypropyl, 3-ethoxypropyl, 3- propoxypropyl, 3-isopropoxypropyl, 3-n-butoxypropyl, 3-sec-butoxypropyl, 3-isobutoxypropyl, 3- tert-butoxypropyl and the like.

The term "Ci-C4-haloalkoxy-Ci-C4-alkyl" as used herein is a straight-chain or branched alkyl group having from 1 to 4 carbon atoms, wherein one of the hydrogen atoms is replaced by a Ci-C4-alkoxy group and wherein at least one, e.g. 1 , 2, 3, 4 or all of the remaining hydrogen atoms, either in the alkoxy moiety or in the alkyl moiety or in both, are replaced by halogen atoms. Examples are difluoromethoxymethyl (CHF2OCH2), trifluoromethoxymethyl, 1 - difluoromethoxyethyl, 1 -trifluoromethoxyethyl, 2-difluoromethoxyethyl, 2-trifluoromethoxyethyl, difluoro(methoxy)methyl (CH3OCF2), 1 ,1 -difluoro-2-methoxyethyl, 2,2-difluoro-2-methoxyethyl and the like.

The term "C _n -C _m -alkoxycarbonyl" is a C _n -C _m -alkoxy group, as defined above, attached via a carbonyl group atom. Ci-C2-Alkoxycarbonyl is methoxycarbonyl or ethoxycarbonyl. C1-C4- Alkoxy is, for example, methoxycarbonyl, ethoxycarbonyl, n-propoxycarbonyl, 1 - methylethoxycarbonyl, butoxycarbonyl, 1 -methylpropoxycarbonyl, 2-methylpropoxycarbonyl or 1 ,1 -dimethylethoxycarbonyl. Ci-C6-Alkoxycarbonyl includes the meanings given for C1-C4- alkoxycarbonyl and also includes, for example, pentoxycarbonyl, 1 -methylbutoxycarbonyl, 2-methylbutoxycarbonyl, 3-methylbutoxycarbonyl, 1 ,1 -dimethylpropoxycarbonyl, 1 ,2- dimethylpropoxycarbonyl, 2,2-dimethylpropoxycarbonyl, 1 -ethylpropoxycarbonyl,

hexoxycarbonyl, 1 -methylpentoxycarbonyl, 2-methylpentoxycarbonyl, 3-methylpentoxycarbonyl, 4-methylpentoxycarbonyl, 1 ,1 -dimethylbutoxycarbonyl, 1 ,2-dimethylbutoxycarbonyl,

1 ,3-dimethylbutoxycarbonyl, 2,2-dimethylbutoxycarbonyl, 2,3-dimethylbutoxycarbonyl,

3,3-dimethylbutoxycarbonyl, 1 -ethylbutoxy, 2-ethylbutoxycarbonyl, 1 ,1 ,2- trimethylpropoxycarbonyl, 1 ,2,2-trimethylpropoxycarbonyl, 1 -ethyl-1 -methylpropoxycarbonyl or 1 -ethyl-2-methylpropoxycarbonyl.

The term "aryl" as used herein refers to an aromatic hydrocarbon radical such as naphthyl or in particular phenyl.

The term "3- to 6-membered carbocyclic ring" as used herein refers to cyclopropane, cyclobutane, cyclopentane and cyclohexane rings. The term "3- to 7-membered carbocyclic ring" as used herein refers to cyclopropane, cyclobutane, cyclopentane, cyclohexane and cycloheptane rings.

The term "3-, 4-, 5-, 6- or 7-membered saturated, partially unsaturated or aromatic heterocyclic ring containing 1 , 2, 3 or 4 heteroatoms" or "containing heteroatom groups", wherein those heteroatom(s) (group(s)) are selected from N, O, S, NO, SO and SO2 and are ring members, as used herein refers to monocyclic radicals, the monocyclic radicals being saturated, partially unsaturated or aromatic. The heterocyclic radical may be attached to the remainder of the molecule via a carbon ring member or via a nitrogen ring member.

Examples of 3-, 4-, 5-, 6- or 7-membered saturated heterocyclic rings include: oxiranyl, aziridinyl, azetidinyl, 2 tetrahydrofuranyl, 3-tetrahydrofuranyl, 2 tetrahydrothienyl, 3

tetrahydrothienyl, 2-pyrrolidinyl, 3-pyrrolidinyl, 3 pyrazolidinyl, 4 pyrazolidinyl, 5-pyrazolidinyl, 2 imidazolidinyl, 4 imidazolidinyl, 2-oxazolidinyl, 4-oxazolidinyl, 5 oxazolidinyl, 3-isoxazolidinyl, 4 isoxazolidinyl, 5 isoxazolidinyl, 2 thiazolidinyl, 4-thiazolidinyl, 5-thiazolidinyl, 3 isothiazolidinyl, 4- isothiazolidinyl, 5 isothiazolidinyl, 1 ,2,4-oxadiazolidin-3-yl, 1 ,2,4 oxadiazolidin 5 yl, 1 ,2,4- thiadiazolidin-3-yl, 1 ,2,4 thiadiazolidin-5-yl, 1 ,2,4 triazolidin-3-yl, 1 ,3,4-oxadiazolidin-2-yl, 1 ,3,4 thiadiazolidin-2-yl, 1 ,3,4 triazolidin-2-yl, 2-tetrahydropyranyl, 4 tetrahydropyranyl, 1 ,3-dioxan-5- yl, 1 ,4-dioxan-2-yl, 2-piperidinyl, 3-piperidinyl, 4-piperidinyl, 3-hexahydropyridazinyl, 4 hexahydropyridazinyl, 2-hexahydropyrimidinyl, 4-hexahydropyrimidinyl, 5 hexahydropyrimidinyl, 2-piperazinyl, 1 ,3,5-hexahydrotriazin-2-yl and 1 ,2,4 hexahydrotriazin-3-yl, 2-morpholinyl, 3- morpholinyl, 2-thiomorpholinyl, 3-thiomorpholinyl, 1 -oxothiomorpholin-2-yl, 1 -oxothiomorpholin-

3- yl, 1 ,1 -dioxothiomorpholin-2-yl, 1 ,1 -dioxothiomorpholin-3-yl, hexahydroazepin-1 -, -2-, -3- or -4- yl, hexahydrooxepinyl, hexahydro-1 ,3-diazepinyl, hexahydro-1 ,4-diazepinyl, hexahydro-1 ,3- oxazepinyl, hexahydro-1 ,4-oxazepinyl, hexahydro-1 ,3-dioxepinyl, hexahydro-1 ,4-dioxepinyl and the like. Examples of 3-, 4-, 5-, 6- or 7-membered partially unsaturated heterocyclic rings include: 2,3-dihydrofur-2-yl, 2,3-dihydrofur-3-yl, 2,5-dihydrofur-2-yl, 2,5-dihydrofur-3-yl, 2,3- dihydrothien-2-yl, 2,3-dihydrothien-3-yl, 2,5-dihydrothien-2-yl, 2,5-dihydrothien-3-yl, 2-pyrrolin-2- yl, 2-pyrrolin-3-yl, 3 pyrrolin-2-yl, 3-pyrrolin-3-yl, 2-isoxazolin-3-yl, 3-isoxazolin-3-yl, 4 isoxazolin 3 yl, 2-isoxazolin-4-yl, 3-isoxazolin-4-yl, 4-isoxazolin-4-yl, 2 isoxazolin-5-yl, 3-isoxazolin-5-yl, 4- isoxazolin-5-yl, 2-isothiazolin-3-yl, 3 isothiazolin-3-yl, 4-isothiazolin-3-yl, 2-isothiazolin-4-yl, 3- isothiazolin-4-yl, 4 isothiazolin-4-yl, 2-isothiazolin-5-yl, 3-isothiazolin-5-yl, 4-isothiazolin-5-yl, 2,3 dihydropyrazol-1 -yl, 2,3-dihydropyrazol-2-yl, 2,3-dihydropyrazol-3-yl, 2,3 dihydropyrazol-4-yl, 2,3-dihydropyrazol-5-yl, 3,4-dihydropyrazol-1 -yl, 3,4 dihydropyrazol-3-yl, 3,4-dihydropyrazol-4- yl, 3,4-dihydropyrazol-5-yl, 4,5 dihydropyrazol-1 -yl, 4,5-dihydropyrazol-3-yl, 4,5-dihydropyrazol- 4-yl, 4,5 dihydropyrazol-5-yl, 2,3-dihydrooxazol-2-yl, 2,3-dihydrooxazol-3-yl, 2,3 dihydrooxazol-

4- yl, 2,3-dihydrooxazol-5-yl, 3,4-dihydrooxazol-2-yl, 3,4 dihydrooxazol-3-yl, 3,4-dihydrooxazol-4- yl, 3,4-dihydrooxazol-5-yl, 3,4 dihydrooxazol-2-yl, 3,4-dihydrooxazol-3-yl, 3,4-dihydrooxazol-4- yl, 2-, 3-, 4-, 5- or 6-di- or tetrahydropyridinyl, 3-di- or tetrahydropyridazinyl, 4 di- or

tetrahydropyridazinyl, 2-di- or tetrahydropyrimidinyl, 4-di- or tetrahydropyrimidinyl, 5 di- or tetrahydropyrimidinyl, di- or tetrahydropyrazinyl, 1 ,3,5-di- or tetrahydrotriazin-2-yl, 1 ,2, 4-di- or tetrahydrotriazin-3-yl, 2,3,4,5-tetrahydro[1 H]azepin-1 -, -2-, -3-, -4-, -5-, -6- or -7-yl, 3,4,5,6- tetrahydro[2H]azepin-2-, -3-, -4-, -5-, -6- or -7-yl, 2,3,4,7 tetrahydro[1 H]azepin-1 -, -2-, -3-, -4-, -5- , -6- or -7-yl, 2,3,6,7 tetrahydro[1 H]azepin-1 -, -2-, -3-, -4-, -5-, -6- or -7-yl, tetrahydrooxepinyl, such as 2,3,4, 5-tetrahydro[1 H]oxepin-2-, -3-, -4-, -5-, -6- or -7-yl, 2,3,4,7 tetrahydro[1 H]oxepin-2- , -3-, -4-, -5-, -6- or -7-yl, 2,3,6,7 tetrahydro[1 H]oxepin-2-, -3-, -4-, -5-, -6- or -7-yl, tetrahydro-1 ,3- diazepinyl, tetrahydro-1 ,4-diazepinyl, tetrahydro-1 ,3-oxazepinyl, tetrahydro-1 ,4-oxazepinyl, tetrahydro-1 ,3-dioxepinyl and tetrahydro-1 ,4-dioxepinyl.

Examples of 5- or 6-membered aromatic heterocyclic rings, also termed heteroaromatic rings or hetaryl, include: 2-furyl, 3-furyl, 2-thienyl, 3-thienyl, 2-pyrrolyl, 3-pyrrolyl, 3-pyrazolyl, 4- pyrazo-"lyl, 5-pyrazolyl, 2-oxazolyl, 4-oxazolyl, 5-oxazolyl, 2-thiazolyl, 4 thiazolyl, 5-thiazo-"lyl, 2- imidazolyl, 4-imidazolyl, 1 ,3,4-triazol-2-yl, 2-pyridinyl, 3-pyridinyl, 4-pyridinyl, 3-pyridazinyl, 4- pyridazinyl, 2-pyrimidinyl, 4-pyrimidinyl, 5-pyrimidinyl and 2-pyrazinyl.

A "C2-Cm-alkylene" is divalent branched or preferably non-branched or linear saturated aliphatic chain having 2 to m, e.g. 2 to 7 carbon atoms, for example CH2CH2, -CH(CH3)-, CH2CH2CH2, CH(CH ₃ )CH ₂ , CH ₂ CH(CH ₃ ), CH2CH2CH2CH2, CH2CH2CH2CH2CH2,

CH2CH2CH2CH2CH2CH2, and CH2CH2CH2CH2CH2CH2CH2.

The term "saturated or partially unsaturated 3- to 7-membered heterocyclodiyl" relates to a bivalent saturated or partially unsaturated 3- to 7-membered heterocyclic radical, containing 1 , 2, 3 or 4 heteroatoms" or "containing heteroatom groups", wherein those heteroatom(s)

(group(s)) are selected from N, O, S, NO, SO and SO2 and are ring members. The bivalent heterocyclic radical may be attached to the remainder of the molecule via a carbon ring member or via a nitrogen ring member. Examples of 3-, 4-, 5-, 6- or 7-membered saturated or partially unsaturated bivalent heterocyclic radicals include: oxirandiyl, oxetandiyl, tetrahydrofurandiyl, 2,3-dihydrofurandiyl, 2,5-dihydrofurandiyl, tetrahydrothienyl, 2,3-dihydrothienyl, 2,5- dihydrothienyl, 1 ,3-dioxolandiyl, 1 ,3-oxothiolandiyl, 1 ,3-dithiolandiyl, 1 ,4-dioxandiyl, 1 ,4- oxothiandiyl, pyrrolidindiyl, piperidindiyl, piperazindiyl, morpholindiyl, thiomorpholindiyl, azepindiyl, 1 ,3,5-trioxandiyl, pyrrolindiyl, 1 ,3-oxazolindiyl, 1 ,3-thiazolindiyl, isoxazolindiyl, isothiazolindiyl, in particular oxiran-2,2-diyl, oxiran-2,3-diyl, oxetan-2,2-diyl, oxetan-2,3-diyl, oxetan-2,4-diyl, tetrahydrofuran-2,3-diyl, tetrahydrofuran-2,-5-diyl, tetrahydrofuran-2,4-diyl, tetrahydrofuran-3,4-diyl, 2,3-dihydrofuran-2,3-diyl, 2,5-dihydrofur-2,5-diyl, 2,3-dihydrothien-2,3- diyl, 2,3 dihydrothien-2,5-diyl, 2,5 dihydrothien-2,5-yl, 2,5-dihydrothien-2,3-diyl, 2-pyrrolin-2,5- diyl, 2-pyrrolin-2,3-diyl, 3-pyrrolin-2,5-diyl, 3-py rro I i n-2 ,3-d iy 1 , 2-isoxazolin-3,4-diyl, 3-isoxazolin- 3,5-diyl, 4-isoxazolin-3,5-diyl.

The term "5- or 6-membered hetarylene" relates to a bivaltent heteroaromatic radical, containing 1 , 2, 3 or 4 heteroatoms which are selected from N, O and S as ring members. The bivalent heteroaromatic radical may be attached to the remainder of the molecule via a carbon ring member or via a nitrogen ring member. Examples of bivalent heteroaromatic radicals include: pyridine-2,6-diyl, pyridine-2,3-diyl, pyridine-2,4-diyl, pyridine-3,4-diyl, pyri d i ne-3 , 5-d iy I , pyrimidin-2,4-diyl, pyri m id i n-2 , 5-d iy I , pyrimidin-4,5-diyl, pyrimidin-4,6-diyl, pyrazin-2,6-diyl, pyrazin-2,3-diyl or pyrazin-2,5-diyl, thiophen-2,5-diyl, thiophen-2,3-diyl, thiophen-2,4-diyl, thiophen-3,4-diyl, furan-2,5-diyl, furan-2,3-diyl, furan-2,4-diyl, furan-3,4-diyl, oxazol-2,4-diyl, oxazol-2,5-diyl, oxazol-4,5-diyl, thiazol-2,4-diyl, thiazol-2,5-diyl, thiazol-4,5-diyl, isoxazol-3,4-diyl, isoxazol-3,5-diyl, isoxazol-4,5-diyl, isothiazol-3,4-diyl, isothiazol-3,5-diyl, isothiazol-4,5-diyl, pyrrol-1 ,2-diyl, pyrrol-1 ,3-diyl, pyrrol-2,3-diyl, pyrrol-2,4-diyl, pyrrol-2,5-diyl, pyrrol-3,4-diyl, 1 H- imidazole-1 ,2-diyl, 1 H-imidazol-1 ,4-diyl, 1 H-imidazole-1 ,5-diyl, 1 H-imidazole-2,4-diyl or 1 H- imidazole-4,5-diyl.

Embodiments of the present invention as well preferred compounds of the present invention are outlined in the following paragraphs. The remarks made below concerning preferred embodiments of the variables of the compounds of formula (I), especially with respect to their substituents X, W ¹ , W ² , W ³ , W ⁴ , Het, R ¹ , R ² , R ³ , R ⁴ and R ⁵ and the variables k and m are valid both on their own and, in particular, in every possible combination with each other.

When # appears in a formula showing a preferred substructure of a compound of the present invention, it denotes the attachment bond in the remainder molecule.

Preferred are compounds of formula (I), wherein Het is selected from the group consisting of radicals of formulae Het-1 to Het-24, with preference given to compounds of the formula (I), their stereoisomers, there tautomers and their salts, where Het is selected from the radicals of the formulae Het-1 , Het-1 1 and Het-24:

Het-1 Het-2 Het-3 Het-4 Het-5

Het-6 Het-7 Het-8 Het-9 Het-10

Het-11 Het-12 Het-13 Het-14 Het-15

Het-16 Het-17 Het-18 Het-19 Het-20

Het-21 Het-22 Het-23 Het-24 wherein # denotes the bond in formula (I), and wherein R ⁶ and k are as defined above and where R ^6a is hydrogen or has one of the meanings given for R ⁶ and where R ^6b is hydrogen or a C-bound radical mentioned as R ⁶ and where R ^6b is in particular hydrogen, Ci-C4-alkyl or C1-C4- haloalkyl. In particular k is 0, 1 or 2, especially 0 or 1 . In formulae Het-1 , Het-2, Het-3, Het-4, Het-7, Het-8, Het-9, Het-10, Het-1 1 , Het-18 and Het-21 , k is especially 1. In particular R ^6a in formulae Het-12, Het-13, Het-14, Het-16, Het-17, Het-19, Het 20 and Het-22 is different from hydrogen.

Irrespectively of its occurrence, R ⁶ is preferably selected from the group consisting of halogen, cyano, Ci-C6-alkyl, Cs-Cs-cycloalkyl, C2-C6-alkenyl, C2-C6-alkynyl, wherein the carbon atoms of the aforementioned aliphatic and cycloaliphatic radicals may optionally be partly or completely halogenated, in particular by fluorine or chlorine, or may further substituted independently from one another with one or more R ⁷ , or R ⁶ may also be a radical selected from the group consisting of OR ⁸ , N R ^17a R ^17b , S(0) _n R ⁸ , S(0) _n N R ^7a R ^7b , C(=0)R ^7a , C(=0)N R ^7a R ⁷ , C(=0)OR ⁸ , C(=S)R ^7a , C(=S)N R ^7a R ⁷ , C(=N R ⁷ )R ^7a , C(=N R ⁷ )N R ^7a R ⁷ . Irrespectively of its occurrence, R ⁶ is in particular selected from the group consisting of halogen, such as chlorine or fluorine, Ci-C4-alkyl, such as methyl or ethyl, Ci-C4-alkoxy, such as methoxy or ethoxy, C1-C4- haloalkoxy, such as difluoromethoxy or trifluoromethoxy, and Ci-C4-haloalkyl, such as difluoromethyl, trifluoromethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl or pentafluoroethyl, more preferably from halogen, Ci-C4-alkyl and Ci-C4-haloalkyl, even more preferably from fluorine, chlorine, Ci-C2-alkyl, such as methyl or ethyl and Ci-C2-haloalkyl such as difluoromethyl, trifluoromethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl or pentafluoroethyl.

Irrespectively of its occurrence, R ^6a is preferably selected from the group consisting of hydrogen, halogen, cyano, Ci-C6-alkyl, Cs-Cs-cycloalkyl, C2-C6-alkenyl and C2-C6-alkynyl, wherein the carbon atoms of the aforementioned aliphatic and cycloaliphatic radicals may optionally be partly or completely halogenated, in particular by fluorine or chlorine, or may further substituted independently from one another with one or more R ⁷ , or R ^6a may also be a radical selected from the group consisting of OR ⁸ , N R ^17a R ^17b , S(0) _n R ⁸ , S(0) _n N R ^17a R ^17b ,

C(=0)R ^7a , C(=0)N R ^7a R ⁷ , C(=0)OR ⁸ , C(=S)R ^7a , C(=S)N R ^7a R ⁷ , C(=N R ⁷ )R ^7a ,

C(=N R ¹⁷ )N R ^17a R ^17b . Irrespectively of its occurrence, R ^6a is in particular selected from the group consisting of hydrogen, halogen, such as chlorine or fluorine, Ci-C4-alkyl, such as methyl or ethyl, Ci-C4-alkoxy, such as methoxy or ethoxy, Ci-C4-haloalkoxy, such as difluoromethoxy or trifluoromethoxy, and Ci-C4-haloalkyl, such as difluoromethyl, trifluoromethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl or pentafluoroethyl, more preferably from halogen, Ci-C4-alkyl and C1-C4- haloalkyi, even more preferably from fluorine, chlorine, Ci-C2-alkyl, such as methyl or ethyl and Ci-C2-haloalkyl such as difluoromethyl, trifluoromethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl or pentafluoroethyl.

Irrespectively of its occurrence, R ^6b is in particular selected from the group consisting of hydrogen, Ci-C4-alkyl, such as methyl or ethyl, and Ci-C4-haloalkyl, such as difluoromethyl, trifluoromethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl or pentafluoroethyl, more preferably C1-C2- alkyl, such as methyl or ethyl and Ci-C2-haloalkyl such as difluoromethyl, trifluoromethyl, 2,2- difluoroethyl, 2,2,2-trifluoroethyl or pentafluoroethyl.

Particularly preferred are compounds of formula (I), wherein Het is selected from the group consistin of radicals of formulae Het-1 , Het-1 1 a and Het-24,

Het-1 Het-11a Het-24 where

R ⁶ is selected from the group consisting of halogen, such as chlorine or fluorine, C1-C4- alkyl, such as methyl or ethyl, Ci-C4-alkoxy, such as methoxy or ethoxy, C1-C4- haloalkoxy, such as difluoromethoxy or trifluoromethoxy, and Ci-C4-haloalkyl, such as difluoromethyl, trifluoromethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl or pentafluoroethyl, more preferably from halogen, Ci-C4-alkyl and Ci-C4-haloalkyl, even more preferably from fluorine, chlorine, Ci-C2-alkyl, such as methyl or ethyl and Ci-C2-haloalkyl such as difluoromethyl, trifluoromethyl, 2,2-difluoroethyl, 2,2,2- trifluoroethyl or pentafluoroethyl; and where

R ^6a is selected from the group consisting of hydrogen, halogen, such as chlorine or fluorine, Ci-C4-alkyl, such as methyl or ethyl, Ci-C4-alkoxy, such as methoxy or ethoxy, Ci-C4-haloalkoxy, such as difluoromethoxy or trifluoromethoxy, and C1-C4- haloalkyl, such as difluoromethyl, trifluoromethyl, 2,2-difluoroethyl, 2,2,2- trifluoroethyl or pentafluoroethyl, more preferably from halogen, Ci-C4-alkyl and Ci-

C4-haloalkyl, even more preferably from fluorine, chlorine, Ci-C2-alkyl, such as methyl or ethyl and Ci-C2-haloalkyl such as difluoromethyl, trifluoromethyl, 2,2- difluoroethyl, 2,2,2-trifluoroethyl or pentafluoroethyl and

k is 0, 1 or 2.

A particularly preferred group of embodiments relates to compounds of formula (I) to the stereoisomers, the tautomers and to the salts thereof, wherein Het is a radical of formula Het-1 , where k is 0, 1 or 2, in particular 1 or 2 and especially 1 and where R ⁶ is as defined above and in particular selected from the group consisting of halogen, such as chlorine or fluorine, C1-C4- alkyl, such as methyl or ethyl, Ci-C4-alkoxy, such as methoxy or ethoxy, Ci-C4-haloalkoxy, such as difluoromethoxy or trifluoromethoxy, and Ci-C4-haloalkyl, such as difluoromethyl,

trifluoromethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl or pentafluoroethyl, more preferably from halogen, Ci-C4-alkyl and Ci-C4-haloalkyl, even more preferably from fluorine, chlorine, C1-C2- alkyl, such as methyl or ethyl and Ci-C2-haloalkyl such as difluoromethyl, trifluoromethyl, 2,2- difluoroethyl, 2,2,2-trifluoroethyl or pentafluoroethyl. Amongst the compounds of this particular group of embodiments, a particular sub-group of embodiments relates to compounds of the formula (I), to the stereoisomers, the tautomers and to the salts thereof, wherein Het is a radical of formula Het-1 a

where

R ⁶ is as defined above and in particular selected from the group consisting of halogen, such as chlorine or fluorine, Ci-C4-alkyl, such as methyl or ethyl, and C1-C4- haloalkyl, such as difluoromethyl, trifluoromethyl, 2,2-difluoroethyl, 2,2,2- trifluoroethyl or pentafluoroethyl, and even more preferably from fluorine, chlorine, Ci-C2-alkyl, such as methyl or ethyl and Ci-C2-haloalkyl such as difluoromethyl, trifluoromethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl or pentafluoroethyl; R ^6a is as defined above and in particular selected from the group consisting of hydrogen, halogen, such as chlorine or fluorine and Ci-C4-alkyl, such as methyl or ethyl, more preferably is hydrogen.

A special embodiment of the radical Het-1 a is 6-chloropyridin-3-yl, i.e. R ^6a is hydrogen and R ⁶ is chlorine. A further special embodiment of the radical Het-1 a is 6-(trifluoromethyl)pyridin-3- yl, i.e. R ^6a is hydrogen and R ⁶ is trifluoromethyl.

Another particularly preferred group of embodiments relates to compounds of formula (I) to the stereoisomers, the tautomers and to the salts thereof, wherein Het is a radical of formula Het-1 1 , where k is 0, 1 or 2, in particular 0 or 1 , and where Het is in particular a radical of formula Het-1 1 a,

where R ^6a is as defined above and wherein R ^6a is in particular selected from the group consisting of hydrogen, halogen, such as chlorine or fluorine, Ci-C4-alkyl, such as methyl or ethyl, Ci-C4-alkoxy, such as methoxy or ethoxy, Ci-C4-haloalkoxy, such as difluoromethoxy or trifluoromethoxy, and Ci-C4-haloalkyl, such as difluoromethyl, trifluoromethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl or pentafluoroethyl, more preferably from halogen, Ci-C4-alkyl and C1-C4- haloalkyl, even more preferably from fluorine, chlorine, Ci-C2-alkyl, such as methyl or ethyl and Ci-C2-haloalkyl such as difluoromethyl, trifluoromethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl or pentafluoroethyl. A special embodiment of the radical Het-1 1 a is 2-chlorothiazol-5-yl, i.e. R ^6a is chlorine.

Another particularly preferred group of embodiments relates to compounds of formula (I) to the stereoisomers, the tautomers and to the salts thereof, wherein Het is a radical of formula Het-24, where k is 0, 1 or 2, in particular 0 or 1 , and where R ⁶ , if present, is as defined above and in particular selected from the group consisting of halogen, such as chlorine or fluorine, Ci- C4-alkyl, such as methyl or ethyl, and Ci-C4-haloalkyl, such as difluoromethyl, trifluoromethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl or pentafluoroethyl, and even more preferably from fluorine, chlorine, Ci-C2-alkyl, such as methyl or ethyl and Ci-C2-haloalkyl such as difluoromethyl, trifluoromethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl or pentafluoroethyl.

Preferred are compounds of formula (I), wherein R ¹ and R ² are independently from each other selected from the group consisting of hydrogen, halogen, such as fluorine or chlorine, CN, Ci-C6-alkyl, in particular Ci-C4-alkyl, such as methyl, ethyl, n-propyl or isopropyl, C3-C6- cycloalkyl, such as cyclopropyl or cyclobutyl, Ci-C6-haloalkyl, in particular Ci-C2-haloalkyl, such as fluoromethyl, difluoromethyl, trifluoromethyl, 1 ,1 -difluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl or 2,2,2-trifluoroethyl, or C3-C6-halocycloalkyl such as 1 -fluorocyclopropyl or 2,2- difluorocyclopropyl.

Preferred are also compounds of formula (I), wherein R ¹ and R ² may together be

=CR ¹³ R ¹⁴ .

Preferred are also compounds of formula (I), wherein R ¹ and R ² form, together with the carbon atom, which they attached to, a 3- to 5-membered saturated carbocyclic ring such as cyclopropyl, cyclobutyl or cyclopentyl. Even more preferred are compounds of formula (I), wherein R ¹ and R ² are independently from each other selected from the group consisting of hydrogen, halogen, cyano, Ci-C3-alkyl, such as methyl, ethyl or isopropyl, or Ci-C3-haloalkyl such as fluoromethyl, difluoromethyl, trifluoromethyl, 1 ,1 -difluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl or 2,2,2-trifluoroethyl.

Preferably at least one of the radicals R ¹ and R ² is hydrogen.

Especially more preferred are compounds of formula (I), wherein R ¹ and R ² are both hydrogen.

In particular groups of embodiments, the group D in formula (I) is a group D ^a which is linear Ci-C6-alkanediyl, in particular linear Ci-C4-alkanediyl, such as Chb, CH2CH2 or

CH2CH2CH2, which is unsubstituted or substituted with 1 , 2, 3, 4, 5 or 6, in particular 1 , 2 or 3, identical or different radicals R ^D1 .

In further particular groups of embodiments, the group D in formula (I) is a group D ^b which is linear C2-C6-alkenediyl, in particular linear C2-C3-alkenediyl, such as CH=CH, CH=CH-CH2 or CH2-CH=CH-CH2, which is unsubstituted or substituted with 1 , 2, 3, 4, 5 or 6, in particular 1 , 2 or 3, identical or different radicals R ^D1 .

In further particular groups of embodiments, the group D in formula (I) is a group D ^c which is linear C2-C6-alkynediyl, in particular linear C2-C4-alkynediyl, such as C≡C, C≡C-CH2 or

CH2-C≡C-CH2, which is unsubstituted or substituted with 1 , 2, 3, 4, 5 or 6, in particular 1 , 2 or 3, identical or different radicals R ^D1 .

In further particular groups of embodiments, the group D in formula (I) is a group D ^d which is linear C3-C6-cycloalkanediyl, in particular C3-C6-cycloalkane-1 ,1 -diyl, C3-C6-cycloalkane-1 ,2- diyl, or C3-C6-cycloalkane-1 ,3-diyl, which is unsubstituted or substituted with 1 , 2, 3, 4, 5 or 6, in particular 1 , 2 or 3, identical or different radicals R ^D2 .

In further particular groups of embodiments, the group D in formula (I) is a group D ^e which is saturated 3-, 4-, 5- or 6-membered heterocyclodiyl, in particular saturated 3-, 4-, 5- or 6- membered ipso-, ortho- or meta-heterocyclodiyl, such as oxiran-2,2-diyl, oxetan-2,2-diyl, tetrahydrofuran-2,2-diyl, tetrahydrofuran-3,3-diyl, oxiran-2,3-diyl, oxetan-2,3-diyl, oxetan-2,4- diyl, tetrahydrofuran-2,3-diyl, tetrahydrofuran-2,4-diyl, tetrahydrofuran-2,5-diyl, tetrahydrofuran- 3,4-diyl, oxan-2,6-diyl, oxan-2,3-diyl, oxan-2,4-diyl or oxan-2,5-diyl, which is unsubstituted or substituted with 1 , 2, 3, 4, 5 or 6, in particular 1 , 2 or 3, identical or different radicals R ^D2 .

In further particular groups of embodiments, the group D in formula (I) is a group D ^f which is phenylene, in particular 1 ,2-phenylene, 1 ,3-phenylene or 1 ,4-phenylene, which is

unsubstituted or substituted with 1 , 2, 3 or 4 radicals R ^D3 .

In further particular groups of embodiments, the group D in formula (I) is a group Ds which is 5- or 6-membered hetarylene, in particular 6-membered hetarylene having 1 or 2 nitrogen atoms as ring memberes, such as pyridine-2,6-diyl, pyridine-2,3-diyl, pyridine-2,4-diyl, pyridine- 3,4-diyl, pyridine-3,5-diyl, pyrimidin-2,4-diyl, py ri m id i n-2 , 5-d iy I , py ri m id i n-4 , 5-d iy I , pyrimidin-4,6- diyl, pyrazin-2,6-diyl, pyrazin-2,3-diyl or pyrazin-2,5-diyl, which is unsubstituted or substituted with 1 , 2, 3 or 4 radicals R ^D3 .

In the context of groups D ^a , D ^b and D ^c the radical R ^D1 is preferably selected from the group consisting of halogen, such as fluorine or chlorine, CN, Ci-C4-alkyl, such as methyl or ethyl, Ci- C4-haloalkyl, such as difluoromethyl or trifluoromethyl, Ci-C4-alkoxy, such as methoxy or ethoxy, Ci-C4-haloalkoxy, such as difluoromethoxy or trifluoromethoxy, C3-C6-cycloalkyl, such as cyclopropyl or cyclobutyl, and phenyl, which is unsubstituted or carries 1 , 2, 3 or 4 radicals, selected from the group consisting of halogen, Ci-C4-alkyl, Ci-C4-haloalkyl, Ci-C4-alkoxy and Ci-C4-haloalkoxy or two radicals R ^D1 , which are bound to the same carbon atom may, together with said carbon atom, form a 3- to 6-membered saturated carbocyclic ring, such as 1 ,1 - cyclopropanediyl, 1 ,1 -cyclobutanediyl, 1 ,1 -cyclopentanediyl or a 3- to 6-membered saturated heterocyclic ring, where the heterocyclic ring has 1 or 2 heteroatoms or heteroatom moieties as ring members which are selected from the group consisting of O and S, such as oxiran-2,2-diyl, oxetan-2,2-diyl, oxetan-3,3-diyl, tetrahydrofuran-2,2-diyl or tetrahydrofuran-3,3-diyl.

In the context of groups D ^d and D ^e the radical R ^D2 is preferably selected from the group consisting of halogen, such as fluorine or chlorine, CN, Ci-C4-alkyl, such as methyl or ethyl, Ci- C4-haloalkyl, such as difluoromethyl or trifluoromethyl, Ci-C4-alkoxy, such as methoxy or ethoxy, Ci-C4-haloalkoxy, such as difluoromethoxy or trifluoromethoxy, C3-C6-cycloalkyl, such as cyclopropyl or cyclobutyl, and phenyl, which is unsubstituted or carries 1 , 2, 3 or 4 radicals, selected from the group consisting of halogen, Ci-C4-alkyl, Ci-C4-haloalkyl, Ci-C4-alkoxy and Ci-C4-haloalkoxy or two radicals R ^D2 , which are bound to the same carbon atom or to adjacent atoms may, together with said carbon atom(s), form a 3- to 6-membered saturated carbocyclic ring, such as 1 ,1 -cyclopropanediyl, 1 ,1 -cyclobutanediyl, 1 ,1 -cyclopentanediyl, 1 ,2- cyclopropanediyl, 1 ,2-cyclobutanediyl, 1 ,2-cyclopentanediyl, 1 ,2-cyclohexanediyl, or a 3- to 6- membered saturated heterocyclic ring, where the heterocyclic ring has 1 or 2 heteroatoms or heteroatom moieties as ring members which are selected from the group consisting of O and S, such as oxiran-2,2-diyl, oxetan-2,2-diyl, oxetan-3,3-diyl, tetrahydrofuran-2,2-diyl or

tetrahydrofuran-3,3-diyl, oxiran-2,3-diyl, oxetan-2,3-diyl, tetrahydrofuran-2,3-diyl or

tetra hyd rof ura n-3 ,4-d iyl .

In the context of groups D ^f and Ds the radical R ^D3 is preferably selected from the group consisting of halogen, such as fluorine or chlorine, CN, Ci-C4-alkyl, such as methyl or ethyl, Ci- C4-haloalkyl, such as difluoromethyl or trifluoromethyl, Ci-C4-alkoxy, such as methoxy or ethoxy, Ci-C4-haloalkoxy, such as difluoromethoxy or trifluoromethoxy, C3-C6-cycloalkyl, such as cyclopropyl or cyclobutyl, and phenyl, which is unsubstituted or carries 1 , 2, 3 or 4 radicals, selected from the group consisting of halogen, Ci-C4-alkyl, Ci-C4-haloalkyl, Ci-C4-alkoxy and Ci-C4-haloalkoxy.

A particularly preferred group A of embodiments relates to compounds of formula (I), their stereoisomers, tautomers and salts, where D is a group D ^a as defined above, where R ^D1 is as defined above and where R ^D1 is in particular selected from the group consisting of halogen, such as fluorine or chlorine, CN, Ci-C4-alkyl, such as methyl or ethyl, Ci-C4-haloalkyl, such as difluoromethyl or trifluoromethyl, Ci-C4-alkoxy, such as methoxy or ethoxy, Ci-C4-haloalkoxy, such as difluoromethoxy or trifluoromethoxy, C3-C6-cycloalkyl, such as cyclopropyl or cyclobutyl, and phenyl, which is unsubstituted or carries 1 , 2, 3 or 4 radicals, selected from the group consisting of halogen, Ci-C4-alkyl, Ci-C4-haloalkyl, Ci-C4-alkoxy and Ci-C4-haloalkoxy or two radicals R ^D1 , which are bound to the same carbon atom may, together with said carbon atom, form a 3- to 6-membered saturated carbocyclic ring, such as 1 ,1 -cyclopropanediyl, 1 ,1 - cyclobutanediyl, 1 ,1 -cyclopentandiyl or a 3- to 6-membered saturated heterocyclic ring, where the heterocyclic ring has 1 or 2 heteroatoms or heteroatom moieties as ring members which are selected from the group consisting of O and S, such as oxiran-2,2-diyl, oxetan-2,2-diyl, oxetan-

3.3- diyl, tetrahydrofuran-2,2-diyl or tetrahydrofuran-3,3-diyl. Amongst the group A of

embodiments, particular examples of D are selected from the group consisting of of CH ₂ , CHF, CF ₂ , CHCN, CH(CH ₃ ), C(CH ₃ ) ₂ , CH ₂ -CH ₂ , cyclopropan-1 ,1 -diyl, cyclobutan-1 ,1 -diyl,

cyclopentan-1 ,1 -diyl, oxetan-2,2-diyl, oxiran-2,2-diyl and A'-CH ₂ , where A is cyclopropan-1 , 1 - diyl and cyclobutan-1 ,1 -diyl.

A particularly preferred group B of embodiments relates to compounds of formula (I), their stereoisomers, tautomers and salts, where D is a group D ^f or Ds as defined above, where R ^D3 is as defined above and where R ^D3 is preferably selected from the group consisting of halogen, such as fluorine or chlorine, CN, Ci-C4-alkyl, such as methyl or ethyl, Ci-C4-haloalkyl, such as difluoromethyl or trifluoromethyl, Ci-C4-alkoxy, such as methoxy or ethoxy, Ci-C4-haloalkoxy, such as difluoromethoxy or trifluoromethoxy, C3-C6-cycloalkyl, such as cyclopropyl or cyclobutyl, and phenyl, which is unsubstituted or carries 1 , 2, 3 or 4 radicals, selected from the group consisting of halogen, Ci-C4-alkyl, Ci-C4-haloalkyl, Ci-C4-alkoxy and Ci-C4-haloalkoxy. Amongst the group B of embodiments, particular examples of D are selected from the group consisting of of 1 ,2-phenylene, 1 ,3-phenylene, 1 ,4-phenylene, pyridindiyl, such as pyridine-2,6-diyl, pyridine-

2.4- diyl or pyridin-3,5-diyl, pyrazindiyl, such as pyrazin-2,6-diyl, and pyrimidindiyl, such as pyrimidin-2,4-diyl or pyri m id i n-4 , 6-d iy I .

A particular group (1 ) of embodiments relates to compounds of formula (I), their stereoisomers, tautomers and salts and to the compounds of groups of embodiments A and B wherein R ³ is selected from the group consisting of hydrogen, Ci-C6-alkyl, in particular C1-C4- alkyl, such as methyl, ethyl, n-propyl, isopropyl,n-butyl, 2-butyl, isobutyl or tert. -butyl, C3-C6- cycloalkyl, such as cydopropyl, cyclobutyl, cyclopentyl or cyclohexyl, Ci-C6-alkyl-0, in particular Ci-C4-alkyl-0, such as methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, 2-butoxy, isobutoxy or tert.butoxy, Ci-C6-alkyl-S, in particular Ci-C4-alkyl-S, such as methylsulfanyl, ethylsulfanyl, n- propylsulfanyl, isopropylsulfanyl,n-butylsulfanyl, 2-butylsulfanyl, isobutylsulfanyl or tert. - butylsulfanyl, C3-C6-cycloalkyl-methyl, such as as cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyl or cyclohexylmethyl, wherein the carbon atoms of each of Ci-C6-alkyl, C3-C6- cycloalkyl, Ci-C6-alkyl-S and C3-C6-cycloalkyl-methyl are unsubstituted, partly or completely halogenated, it being also possible for these radicals to carry 1 or 2 radicals R ⁷ , which are different from Ci-C6-alkyl, it being also possible for cycloalkyi radicals to carry 1 , 2, 3, 4, 5 or 6 Ci-C4-alkyl groups, in particular methyl groups.

In context of group (1 ) of embodiments, R ⁷ is as defined above and in particular selected, independently of each other from CN, Ci-C4-alkyl, such as methyl or ethyl, Ci-C4-alkoxy, such as methoxy or ethoxy, Ci-C4-alkylthio, such as methylsulfanyl or ethylsulfanyl, Ci-C4-haloalkyl, such as difluormethyl, trifluoromethyl, 2,2,2-trifluoroethyl or pentafluoroetyl, Ci-C4-haloalkoxy, such as difluoromethoxy or trifluoromethoxy, and Ci-C4-haloalkylthio such as

trifluoromethylsulfanyl, 2,2,2-trifluoroethylsulfanyl or pentafluoroethylsulfanyl.

Amongst the compounds of the group (1 ) of embodiments, particular preference is given to those compounds of formula I, where R ³ is selected from the group consisting of hydrogen, Ci-C6-alkyl, in particular Ci-C4-alkyl, such as methyl, ethyl, n-propyl, isopropyl,n-butyl, 2-butyl, isobutyl or tert. -butyl, C3-C6-cycloalkyl, such as cydopropyl, cyclobutyl, cyclopentyl or cyclohexyl, Ci-C6-alkyl-S, in particular Ci-C4-alkyl-S, such as methylsulfanyl, ethylsulfanyl, n- propylsulfanyl, isopropylsulfanyl,n-butylsulfanyl, 2-butylsulfanyl, isobutylsulfanyl or tert. - butylsulfanyl and C3-C6-cycloalkyl-methyl, such as as cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyl or cyclohexylmethyl, wherein the carbon atoms of each of Ci-C6-alkyl, C3-C6- cycloalkyl, Ci-C6-alkyl-S and C3-C6-cycloalkyl-methyl are unsubstituted, partly or completely halogenated.

A particular group (2) of embodiments relates to compounds of formula (I), their stereoisomers, tautomers and salts wherein R ³ is selected from the group consisting of phenyl, benzyl, 5- or 6-membered hetaryl, 5- or 6-membered hetaryl-methyl, wherein the 5- or 6- membered hetaryl in the last two radicals comprises 1 , 2, 3 or 4 heteroatoms as ring members, which are selected from oxygen, nitrogen and/or sulfur and wherein phenyl and hetaryl are unsubstituted or carry 1 , 2 or 3 identical or different radicals R ¹⁰ . In context of group (2) of embodiments, R ¹⁰ is as defined above and in particular selected, independently of each other from halogen, such as fluorine or chlorine, CN, Ci-C4-alkyl, such as methyl or ethyl, Ci-C4-alkoxy, such as methoxy or ethoxy, Ci-C4-alkylthio, such as

methylsulfanyl or ethylsulfanyl, Ci-C4-haloalkyl, such as difluormethyl, trifluoromethyl, 2,2,2- trifluoroethyl or pentafluoroetyl, Ci-C4-haloalkoxy, such as difluoromethoxy or trifluoromethoxy, Ci-C4-alkylcarbonyl, such as acetyl or propionyl, Ci-C4-alkoxycarbonyl, such as

methoxycarbonyl or ethoxycarbonyl, and Ci-C4-haloalkylthio such as trifluoromethylsulfanyl, 2,2,2-trifluoroethylsulfanyl or pentafluoroethylsulfanyl.

Amongst the compounds of the group (2) of embodiments, particular preference is given to those compounds of formula I, where R ³ is selected from the group consisting of phenyl, benzyl, 5- or 6-membered hetaryl, 5- or 6-membered hetaryl-methyl, wherein the 5- or 6- membered hetaryl in the last two radicals comprises 1 , 2, 3 or 4 heteroatoms as ring members, which are selected from oxygen, nitrogen and/or sulfur and wherein phenyl and hetaryl are unsubstituted or carry 1 , 2 or 3 identical or different radicals R ¹⁰ , which are selected, independently of each other from halogen, CN, Ci-C4-alkyl, Ci-C4-alkoxy, Ci-C4-alkylthio, C1-C4- haloalkyl, Ci-C4-haloalkoxy, Ci-C4-alkylcarbonyl, Ci-C4-alkoxycarbonyl and Ci-C4-haloalkylthio. In the context of embodiment (2) examples of 5- or 6-membered hetaryl include in particular pyridyl, pyrimidinyl, furyl, thienyl, oxazolyl, thiazolyl, isoxazolyl, isothiazolyl, 1 H-1 ,2,4-triazolyl and 1 H-tetrazolyl.

Preferred are compounds of formula (I), in particular the compounds of embodiments (1 ) and (2) wherein R ⁴ is selected from the group consisting of hydrogen, Ci-C6-alkyl, in particular Ci-C4-alkyl, such as methyl, ethyl, n-propyl, isopropyl,n-butyl, 2-butyl, isobutyl or tert. -butyl, C3- C6-cycloalkyl, such as cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl, Ci-C6-alkyl-0, in particular Ci-C4-alkyl-0, such as methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, 2-butoxy, isobutoxy or tert.butoxy, Ci-C6-alkyl-S, in particular Ci-C4-alkyl-S, such as methylsulfanyl, ethylsulfanyl, n-propylsulfanyl, isopropylsulfanyl,n-butylsulfanyl, 2-butylsulfanyl, isobutylsulfanyl or tert.-butylsulfanyl, C3-C6-cycloalkyl-methyl, such as as cyclopropyl methyl, cyclobutylmethyl, cyclopentylmethyl or cyclohexylmethyl, wherein the carbon atoms of each of Ci-C6-alkyl, C3-C6- cycloalkyl, Ci-C6-alkyl-S and C3-C6-cycloalkyl-methyl are unsubstituted, partly or completely halogenated, it being also possible for these radicals to carry 1 or 2 radicals R ⁷ , which are different from Ci-C6-alkyl, it being also possible for cycloalkyl radicals to carry 1 , 2, 3, 4, 5 or 6 Ci-C4-alkyl groups, in particular methyl groups, or R ⁴ is selected from the group consisting of phenyl, benzyl, 5- or 6-membered hetaryl, 5- or 6-membered hetaryl-methyl, wherein the 5- or 6-membered hetaryl in the last two radicals comprises 1 , 2, 3 or 4 heteroatoms as ring members, which are selected from oxygen, nitrogen and/or sulfur and wherein phenyl and hetaryl are unsubstituted or carry 1 , 2 or 3 identical or different radicals R ¹⁰ , where R ¹⁰ is as defined above and in particular selected, independently of each other from halogen, such as fluorine or chlorine, CN, Ci-C4-alkyl, such as methyl or ethyl, Ci-C4-alkoxy, such as methoxy or ethoxy, Ci-C4-alkylthio, such as methylsulfanyl or ethylsulfanyl, Ci-C4-haloalkyl, such as difluormethyl, trifluoromethyl, 2,2,2-trifluoroethyl or pentafluoroetyl, Ci-C4-haloalkoxy, such as difluoromethoxy or trifluoromethoxy, Ci-C4-alkylcarbonyl, such as acetyl or propionyl, C1-C4- alkoxycarbonyl, such as methoxycarbonyl or ethoxycarbonyl, and Ci-C4-haloalkylthio such as trifluoromethylsulfanyl, 2,2,2-trifluoroethylsulfanyl or pentafluoroethylsulfanyl.

In context of radical R ⁴ , the radical R ⁷ is as defined above and in particular selected, independently of each other from CN, Ci-C4-alkyl, such as methyl or ethyl, Ci-C4-alkoxy, such as methoxy or ethoxy, Ci-C4-alkylthio, such as methylsulfanyl or ethylsulfanyl, Ci-C4-haloalkyl, such as difluormethyl, trifluoromethyl, 2,2,2-trifluoroethyl or pentafluoroetyl, Ci-C4-haloalkoxy, such as difluoromethoxy or trifluoromethoxy, and Ci-C4-haloalkylthio such as

trifluoromethylsulfanyl, 2,2,2-trifluoroethylsulfanyl or pentafluoroethylsulfanyl.

Particularly preferred are compounds of formula (I), in particular the compounds of groups

(1 ) and (2) embodiments wherein R ⁴ is selected from the group consisting of hydrogen, C1-C6- alkyl, in particular Ci-C4-alkyl, such as methyl, ethyl, n-propyl, isopropyl, n-butyl, 2-butyl, isobutyl or tert. -butyl, C3-C6-cycloalkyl, such as cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl, C1-C6- alkyl-S, in particular Ci-C4-alkyl-S, such as methylsulfanyl, ethylsulfanyl, n-propylsulfanyl, isopropylsulfanyl,n-butylsulfanyl, 2-butylsulfanyl, isobutylsulfanyl or tert.-butylsulfanyl and C3-C6- cycloalkyl-methyl, such as as cyclopropyl methyl, cyclobutylmethyl, cyclopentyl methyl or cyclohexyl methyl, wherein the carbon atoms of each of Ci-C6-alkyl, C3-C6-cycloalkyl, C1-C6- alkyl-S and C3-C6-cycloalkyl-methyl are unsubstituted, partly or completely halogenated.

Especially preferred are compounds of formula (I), in particular the compounds of groups (A) and (B) embodiments wherein R ⁴ is selected from the group consisting of hydrogen, C1-C6- alkyl, in particular Ci-C4-alkyl, such as methyl, ethyl, n-propyl, isopropyl, n-butyl, 2-butyl, isobutyl or tert. -butyl and where R ³ is as defined above and in particular selected from the group consisting of hydrogen, Ci-C6-alkyl, in particular Ci-C4-alkyl, such as methyl, ethyl, n-propyl, isopropyl, n-butyl, 2-butyl, isobutyl or tert. -butyl, C3-C6-cycloalkyl, such as cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl, C3-C6-cycloalkyl-methyl, such as cyclopropylmethyl, cyclobutylmethyl, cyclopentyl methyl or cyclohexylmethyl, wherein the carbon atoms of each Ci- C6-alkyl, C3-C6-cycloalkyl and C3-C6-cycloalkylmethyl are unsubstituted, partly or completely halogenated; phenyl, benzyl, 5- or 6-membered hetaryl, 5- or 6-membered hetaryl-methyl, wherein the 5- or 6-membered hetaryl in the last two radicals comprises 1 , 2, 3 or 4

heteroatoms as ring members, which are selected from oxygen, nitrogen and/or sulfur and wherein phenyl and hetaryl are unsubstituted or carry 1 , 2 or 3 identical or different radicals R ¹⁰ , which are selected, independently of each other from halogen, CN, Ci-C4-alkyl, Ci-C4-alkoxy, Ci-C4-alkylthio, Ci-C4-haloalkyl, Ci-C4-haloalkoxy and Ci-C4-haloalkyl, and wherein the term "5- or 6-membered hetaryl" in particular includes the following meanings: pyridyl, pyrimidinyl, furyl, thienyl, oxazolyl, thiazolyl, isoxazolyl, isothiazolyl, 1 H-1 ,2,4-triazolyl and 1 H-tetrazolyl.

Especially preferred are also compounds of formula (I), in particular the compounds of groups (A) and (B) embodiments, wherein R ³ is Ci-C6-alkyl-S, in particular Ci-C4-alkyl-S, such as methylsulfanyl, ethylsulfanyl, n-propylsulfanyl, isopropylsulfanyl,n-butylsulfanyl, 2- butylsulfanyl, isobutylsulfanyl or tert.-butylsulfanyl, and R ⁴ is Ci-C6-alkyl-S, in particular C1-C4- alkyl-S, such as methylsulfanyl, ethylsulfanyl, n-propylsulfanyl, isopropylsulfanyl,n-butylsulfanyl, 2-butylsulfanyl, isobutylsulfanyl or tert.-butylsulfanyl.

Particular subgroups of the compounds of the groups (1 ) and (2) of embodiments are those compounds, where D is in accordance with the definition of the group of embodiments (A). These subgroups of embodiments are hereinafter termed group (1 -A) of embodiments and group (2-A) of embodiments.

A further particular group (3) of embodiments relates to compounds of formula (I), their stereoisomers, tautomers and salts and to the compounds of groups of embodiments A and B wherein R ³ and R ⁴ together form a bivalent radical, selected from the group consisting of C3-C6- alkanediyl, C3-C6-alkenediyl, Q ¹ -C2-Cs-alkanediyl, Q ¹ -C2-Cs-alkenediyl, Q ¹ -C2-C4-alkanediyl-Q ² and Q ¹ -C2-C4-alkenediyl-Q ² , wherein the carbon atom in the six aforementioned radicals are unsubstituted or may carry 1 , 2, 3 or 4 radicals R ^7b , and wherein Q ¹ and Q ² are, independently from each other, selected from O, S and N(R ^7d ) and where R ^7b is as defined above and in particular selected form the group consisting of halogen, such as fluorine or chlorine, and where R ^7d is in particular selected from hydrogen and Ci-C4-alkyl, such as methyl or ethyl.

In group (3) embodiments, R ³ and R ⁴ preferably together form a bivalent radical, selected from the group consisting of C3-C6-alkanediyl, C4-C6-alkenediyl, S-C2-C4-alkanediyl-S and S-C2-C4-alkenediyl-S, and N(R ^7d )-C2-C4-alkanediyl-N(R ^7d ) wherein the carbon atom in the five aforementioned radicals are unsubstituted or may carry 1 , 2, 3 or 4 radicals R ^7b , where R ^7b is as defined above and in particular selected form the group consisting of halogen, such as fluorine or chlorine, and Ci-C4-alkyl, such as methyl or ethyl, and where R ^7d is in particular selected from hydrogen and Ci-C4-alkyl, such as methyl or ethyl.

A further particular subgroup of the compounds of group (3) of embodiments are those compounds, where D is in accordance with the definition of the group of embodiments (A). This particular subgroup is hereinafter termed group (3-A) of embodiments. In formula I and likewise in the groups (1 ), (2) and (3) embodiments and also in groups (A), (B), (1 -A), (2-A) and (3-A) embodiments, the radical Y is preferably O or NR ⁵ , where R ⁵ is as defined above and where R ⁵ is in particular selected from the group consisting of hydrogen, Ci-C6-alkyl, C3-C6-cycloalkyl, Ci-C6-alkylcarbonyl, C3-C6-cycloalkyl-methyl, wherein the carbon atoms of each of the 4 last mentioned radicals are unsubstituted, partly or completely halogenated, phenyl and benzyl, where the phenyl ring in the last two mentioned radicals is unsubstituted or carries 1 , 2, 3 or 4 radicals R ¹⁰ , where R ¹⁰ is as defined above and in particular selected from the group consisting of halogen, CN , Ci-C4-alkyl, Ci-C4-alkoxy, Ci-C4-alkylthio, Ci-C4-haloalkyl, Ci-C4-haloalkoxy and Ci-C4-haloalkylthio. Especially, R ⁵ is selected from the group consisting of hydrogen, Ci-C6-alkyl, in in particular Ci-C4-alkyl, such as methyl, ethyl, n- propyl, isopropyl, n-butyl, 2-butyl, isobutyl or tert. -butyl, and Ci-C6-alkylcarbonyl, in particular Ci- C4-alkylcarbonyl, such as acetyl or propionyl, wherein the carbon atoms of Ci-C6-alkyl and Ci- C6-alkylcarbonyl are unsubstituted, partly or completely halogenated, and where the carbon atoms of Ci-C6-alkyl and Ci-C6-alkylcarbonyl are especially unsubstituted.

If the radical Y is NR ⁵ the radicals R ³ and R ⁵ together may also form a bivalent radical, selected from the group consisting of C2-C6-alkanediyl and C2-C6-alkenediyl, wherein the carbon atom in the two aforementioned radicals are unsubstituted or may carry 1 , 2, 3, 4, 5 or 6 radicals R ^7c , which are as defined above and which are in particular selected from the group consisting of halogen, such as fluorine or chlorine, and Ci-C4-alkyl, such as methyl or ethyl.

In formula (I) and likewise in the groups (1 ), (2) and (3) embodiments and also in groups

(A), (B), (1 -A), (2-A) and (3-A) embodiments, the radical Y is in particular O.

Preferred are compounds of formula (I), and likewise the compounds of groups (1 ), (2) and (3) embodiments and also of groups (A), (B), (1 -A), (2-A) and (3-A) embodiments, wherein W ¹ -W ² -W ³ -W ⁴ represents a carbon chain group connected to N and C=N, which is selected from the group consisting of CR ^w6 =CR ^w5 -CR ^w4 =CR ^w3 , CR ^w6 =CR ^w5 -CHR ^w4 -CHR ^w3 ,

CHR ^w6 -CHR ^w5 -CHR ^w4 -CHR ^w3 , CHR ^w6 -CH R ^w5 -CR ^w4 =CR ^w3 , and CHR ^w6 -CHR ^w5 -CHR ^w4 -CHR ^w3 , where in the five aforementioned radicals the carbon atom which carries R ^w6 is bound to the nitrogen atom and where R ^w3 , R ^w4 , R ^w5 and R ^w6 , independently of each other, have one of the meanings given for R ^w . In this context, R ^w is preferably selected from the group consisting of hydrogen, halogen, such as fluorine or chlorine, CN, Ci-C4-alkyl, such as methyl, ethyl, n-propyl and isopropyl, Ci-C4-haloalkyl, in particular Ci-C2-haloalkyl, such as fluoromethyl,

difluoromethyl, trifluoromethyl, 1 ,1 -difluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl or 2,2,2- trifluoroethyl, Ci-C4-alkoxy, such as methoxy, ethoxy, n-propoxy and isopropoxy, and C1-C4- haloalkoxy, in particular Ci-C2-haloalkoxy, such as fluoromethoxy, difluoromethoxy, trifluoromethoxy, 1 ,1 -difluoroethoxy, 2-fluoroethoxy, 2,2-difluoroethoxy or 2,2,2-trifluoroethoxy. Preferably, at most one of R ^w3 , R ^w4 , R ^w5 and R ^w6 is different from hydrogen.

In particularly preferred groups of embodiments R ^w3 , R ^w4 and R ^w6 are hydrogen while R ^w5 has one of the meanings given for R ^w , and where R ^w5 is in particular selected from the group consisting of hydrogen, halogen, such as fluorine or chlorine, CN, Ci-C4-alkyl, such as methyl, ethyl, n-propyl and isopropyl, Ci-C4-haloalkyl, in particular Ci-C2-haloalkyl, such as fluoromethyl, difluoromethyl, trifluoromethyl, 1 ,1 -difluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl or 2,2,2- trifluoroethyl, Ci-C4-alkoxy, such as methoxy, ethoxy, n-propoxy and isopropoxy, and C1-C4- haloalkoxy, in particular Ci-C2-haloalkoxy, such as fluoromethoxy, difluoromethoxy,

trifluoromethoxy, 1 ,1 -difluoroethoxy, 2-fluoroethoxy, 2,2-difluoroethoxy or 2,2,2-trifluoroethoxy.

In other particularly preferred groups of embodiments R ^w3 , R ^w4 and R ^w5 are hydrogen while R ^w6 has one of the meanings given for R ^w , and where R ^w6 is in particular selected from the group consisting of hydrogen, halogen, such as fluorine or chlorine, CN, Ci-C4-alkyl, such as methyl, ethyl, n-propyl and isopropyl, Ci-C4-haloalkyl, in particular Ci-C2-haloalkyl, such as fluoromethyl, difluoromethyl, trifluoromethyl, 1 ,1 -difluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl or 2,2,2-trifluoroethyl, Ci-C4-alkoxy, such as methoxy, ethoxy, n-propoxy and isopropoxy, and Ci- C4-haloalkoxy, in particular Ci-C2-haloalkoxy, such as fluoromethoxy, difluoromethoxy, trifluoromethoxy, 1 ,1 -difluoroethoxy, 2-fluoroethoxy, 2,2-difluoroethoxy or 2,2,2-trifluoroethoxy.

Especially, all of R ^w3 , R ^w4 , R ^w5 and R ^w6 are hydrogen.

Preferred are compounds of formula (I), and likewise the compounds of groups (1 ), (2) and (3) embodiments and also of groups (A), (B), (1 -A), (2-A) and (3-A), embodiments wherein the moiety of the formula (A)

represents a radical selected from the group consisting of W.Het-1 , W.Het-2, W.Het-3, W.Het-4, W.Het-5, W.Het-6, W.Het-7, W.Het-8, W.Het-9, W.Het-10, W.Het-1 1 and W.Het-12, in where the radical of formula (A) is in particular selected from the radicals W.Het-1 , W.Het-2, W.Het-5, W.Het-6, W.Het-9 and W.Het-10.

W.Het-1 W.Het-2 W.Het-3 W.Het-4

W.Het-5 W.Het-6 W.Het-7 W.Het-8

W.Het-9 W.Het-10 W.Het-11 W.Het-12 wherein # denotes the bond to the remainder of the molecule and where R ¹ , R ² and Het are as defined herein and where R ¹ , R ² and Het, individually or in combination have the meanings given as preferred meanings, and wherein R ^w3 , R ^w4 , ^< R ^w5 and R ^w6 are as defined above and in particular selected from the group consisting of hydrogen, halogen, such as fluorine or chlorine, CN, Ci-C4-alkyl, such as methyl, ethyl, n-propyl and isopropyl, C1-C4- haloalkyl, in particular Ci-C2-haloalkyl, such as fluoromethyl, difluoromethyl, trifluoromethyl, 1 ,1 - difluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl or 2,2,2-trifluoroethyl, Ci-C4-alkoxy, such as methoxy, ethoxy, n-propoxy and isopropoxy, and Ci-C4-haloalkoxy, in particular C1-C2- haloalkoxy, such as fluoromethoxy, difluoromethoxy, trifluoromethoxy, 1 ,1 -difluoroethoxy, 2- fluoroethoxy, 2,2-difluoroethoxy or 2,2,2-trifluoroethoxy.

Particularly preferred are compounds of formula (I), and likewise the compounds of groups (1 ), (2) and (3) embodiments and also of groups (A), (B), (1 -A), (2-A) and (3-A) embodiments, wherein the moiety of the formula A is selected from the group consisting of W.Het-1 , W.Het-5 and W.Het-9, wherein R ^w6 is as defined above and in particular selected from the group consisting of hydrogen, halogen, such as fluorine or chlorine, CN, Ci-C4-alkyl, such as methyl, ethyl, n-propyl and isopropyl, Ci-C4-haloalkyl, in particular Ci-C2-haloalkyl, such as fluoromethyl, difluoromethyl, trifluoromethyl, 1 ,1 -difluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl or 2,2,2-trifluoroethyl, Ci-C4-alkoxy, such as methoxy, ethoxy, n-propoxy and isopropoxy, and Ci- C4-haloalkoxy, in particular Ci-C2-haloalkoxy, such as fluoromethoxy, difluoromethoxy, trifluoromethoxy, 1 ,1 -difluoroethoxy, 2-fluoroethoxy, 2,2-difluoroethoxy or 2,2,2-trifluoroethoxy and where R ^w6 is especially hydrogen.

Likewise, particularly preferred are compounds of formula (I), and likewise the compounds of groups (1 ), (2) and (3) embodiments and also of groups (A), (B), (1 -A), (2-A) and (3-A) embodiments, wherein the moiety of the formula A is selected from the group consisting of W.Het-2, W.Het-6 and W.Het-10, wherein R ^w5 is as defined above and in particular selected from the group consisting of hydrogen, halogen, such as fluorine or chlorine, CN, Ci-C4-alkyl, such as methyl, ethyl, n-propyl and isopropyl, Ci-C4-haloalkyl, in particular Ci-C2-haloalkyl, such as fluoromethyl, difluoromethyl, trifluoromethyl, 1 ,1 -difluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl or 2,2,2-trifluoroethyl, Ci-C4-alkoxy, such as methoxy, ethoxy, n-propoxy and isopropoxy, and Ci-C4-haloalkoxy, in particular Ci-C2-haloalkoxy, such as fluoromethoxy, difluoromethoxy, trifluoromethoxy, 1 ,1 -difluoroethoxy, 2-fluoroethoxy, 2,2-difluoroethoxy or 2,2,2-trifluoroethoxy and where R ^w5 is especially hydrogen.

Likewise, particularly preferred are compounds of formula (I), and likewise the compounds of groups (1 ), (2) and (3) embodiments and also of groups (A), (B), (1 -A), (2-A) and (3-A) embodiments, wherein the moiety of the formula A is selected from the group consisting of W.Het-1 , W.Het-2, W.Het-3 and W.Het-4, especially from the group consisting of W.Het-1 and W.Het-2, wherein R ^w3 , R ^w4 , R ^w5 and R ^w6 , independently of each other, are as defined above and in particular selected from the group consisting of hydrogen, halogen, such as fluorine or chlorine, CN, Ci-C4-alkyl, such as methyl, ethyl, n-propyl and isopropyl, Ci-C4-haloalkyl, in particular Ci-C2-haloalkyl, such as fluoromethyl, difluoromethyl, trifluoromethyl, 1 ,1 -difluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl or 2,2,2-trifluoroethyl, Ci-C4-alkoxy, such as methoxy, ethoxy, n- propoxy and isopropoxy, and Ci-C4-haloalkoxy, in particular Ci-C2-haloalkoxy, such as fluoromethoxy, difluoromethoxy, trifluoromethoxy, 1 ,1 -difluoroethoxy, 2-fluoroethoxy, 2,2- difluoroethoxy or 2,2,2-trifluoroethoxy and where at most one of R ^w3 , R ^w4 , R ^w5 and R ^w6 are especially hydrogen.

In the moieties W.Het-1 , W.Het-2, W.Het-3, W.Het-4, W.Het-5, W.Het-6, W.Het-7, W.Het- 8, W.Het-9, W.Het-10, W.Het-1 1 and W.Het-12, the heterocycle Het is in particular selected from the group consisting of the radicals of formulae Het-1 to Het-24, as defined above, and in particular selected from the group consisting of the radicals of the formulae Het-1 or Het-1 a, Het-1 1 a and Het-24.

In the moieties W. Het-1 , W.Het-2, W.Het-3, W.Het-4, W.Het-5, W.Het-6, W.Het-7, W.Het- 8, W.Het-9, W.Het-10, W.Het-1 1 and W.Het-12, the radicals R ¹ and R ² are, independently from each other, in particular selected from the group consisting of hydrogen, halogen, such as fluorine or chlorine, CN, Ci-C6-alkyl, in particular Ci-C4-alkyl, such as methyl, ethyl, n-propyl or isopropyl, C3-C6-cycloalkyl, such as cyclopropyl or cyclobutyl, Ci-C6-haloalkyl, in particular Ci- C2-haloalkyl, such as fluoromethyl, difluoromethyl, trifluoromethyl, 1 ,1 -difluoroethyl, 2- fluoroethyl, 2,2-difluoroethyl or 2,2,2-trifluoroethyl, or C3-C6-halocycloalkyl such as 1 - fluorocyclopropyl or 2,2-difluorocyclopropyl, or R ¹ and R ² may together be =CR ¹³ R ¹⁴ or R ¹ and R ² form, together with the carbon atom, which they attached to, a 3- to 5 membered saturated carbocyclic ring such as cyclopropyl, cyclobutyl or cyclopentyl.

In particular embodiments of moieties W.Het-1 , W.Het-2, W.Het-3, W.Het-4, W.Het-5, W.Het-6, W.Het-7, W.Het-8, W.Het-9, W.Het-10, W.Het-1 1 and W.Het-12, the radicals R ¹ and R ² are, independently from each other, more particularly selected from the group consisting of hydrogen, halogen, cyano, Ci-C3-alkyl, such as methyl, ethyl or isopropyl, or Ci-C3-haloalkyl such as fluoromethyl, difluoromethyl, trifluoromethyl, 1 ,1 -difluoroethyl, 2-fluoroethyl, 2,2- difluoroethyl or 2,2,2-trifluoroethyl, where in particular at least one of the radicals R ¹ and R ² is hydrogen.

Especially, R ¹ and R ² in the moieties W.Het-1 , W.Het-2, W.Het-3, W.Het-4, W.Het-5,

W.Het-6, W.Het-7, W.Het-8, W.Het-9, W.Het-10, W.Het-1 1 and W.Het-12 are both hydrogen.

A particular group (a) of embodiments relates to compounds of the formula (I), to their stereoisomers, their tautomers and their salts, and likewise to the compounds of groups (1 ), (2), (3), (A), (B), (1 -A), (2-A) and (3-A) embodiments, wherein the moiety of formula (A) represents a radical selected from the group consisting of W.Het-1 , wherein Het is selected from the group consisting of radicals of formulae Het-1 , Het-1 1 a and Het-24.

A further particular group (b) of embodiments relates to compounds of the formula (I), to their stereoisomers, their tautomers and their salts, and likewise to the compounds of groups (1 ), (2), (3), (A), (B), (1 -A), (2-A) and (3-A) embodiments, wherein the moiety of formula (A) represents a radical selected from the group consisting of W.Het-2, wherein Het is selected from the group consisting of radicals of formulae Het-1 , Het-1 1 a and Het-24.

A further particular group (c) of embodiments relates to compounds of the formula (I), to their stereoisomers, their tautomers and their salts, and likewise to the compounds of groups (1 ), (2), (3), (A), (B), (1 -A), (2-A) and (3-A) embodiments, wherein the moiety of formula (A) represents a radical selected from the group consisting of W.Het-5, wherein Het is selected from the group consisting of radicals of formulae Het-1 , Het-1 1 a and Het-24.

A further particular group (d) of embodiments relates to compounds of the formula (I), to their stereoisomers, their tautomers and their salts, and likewise to the compounds of groups (1 ), (2), (3), (A), (B), (1 -A), (2-A) and (3-A) embodiments, wherein the moiety of formula (A) represents a radical selected from the group consisting of W.Het-6, wherein Het is selected from the group consisting of radicals of formulae Het-1 , Het-1 1 a and Het-24.

A further particular group (e) of embodiments relates to compounds of the formula (I), to their stereoisomers, their tautomers and their salts, and likewise to the compounds of groups (1 ), (2), (3), (A), (B), (1 -A), (2-A) and (3-A) embodiments, wherein the moiety of formula (A) represents a radical selected from the group consisting of W.Het-9, wherein Het is selected from the group consisting of radicals of formulae Het-1 , Het-1 1 a and Het-24.

A further particular group (f) of embodiments relates to compounds of the formula (I), to their stereoisomers, their tautomers and their salts, and likewise to the compounds of groups (1 ), (2), (3), (A), (B), (1 -A), (2-A) and (3-A) embodiments, wherein the moiety of formula (A) represents a radical selected from the group consisting of W.Het-10, wherein Het is selected from the group consisting of radicals of formulae Het-1 , Het-1 1 a and Het-24.

A special group (aa) of embodiments relates to compounds of the formula (I), to their stereoisomers, their tautomers and their salts, and likewise to the compounds of groups (1 ), (2), (3), (A), (B), (1 -A), (2-A) and (3-A) embodiments, wherein the moiety of formula (A) represents a radical selected from the group consisting of W.Het-1 , wherein Het is a radical of formula Het- 1 a.

A further special group (ba) of embodiments relates to compounds of the formula (I), to their stereoisomers, their tautomers and their salts, and likewise to the compounds of groups (1 ), (2), (3), (A), (B), (1 -A), (2-A) and (3-A) embodiments, wherein the moiety of formula (A) represents a radical selected from the group consisting of W.Het-2, wherein Het is a radical of formula Het-1 a.

A further special group (ca) of embodiments relates to compounds of the formula (I), to their stereoisomers, their tautomers and their salts, and likewise to the compounds of groups (1 ), (2), (3), (A), (B), (1 -A), (2-A) and (3-A) embodiments, wherein the moiety of formula (A) represents a radical selected from the group consisting of W.Het-5, wherein Het is a radical of formula Het-1 a.

A further special group (da) of embodiments relates to compounds of the formula (I), to their stereoisomers, their tautomers and their salts, and likewise to the compounds of groups (1 ), (2), (3), (A), (B), (1 -A), (2-A) and (3-A) embodiments, wherein the moiety of formula (A) represents a radical selected from the group consisting of W.Het-6, wherein Het is a radical of formula Het-1 a.

A further special group (ea) of embodiments relates to compounds of the formula (I), to their stereoisomers, their tautomers and their salts, and likewise to the compounds of groups (1 ), (2), (3), (A), (B), (1 -A), (2-A) and (3-A) embodiments, wherein the moiety of formula (A) represents a radical selected from the group consisting of W.Het-9, wherein Het is a radical of formula Het-1 a.

A further special group (fa) of embodiments relates to compounds of the formula (I), to their stereoisomers, their tautomers and their salts, and likewise to the compounds of groups (1 ), (2), (3), (A), (B), (1 -A), (2-A) and (3-A) embodiments, wherein the moiety of formula (A) represents a radical selected from the group consisting of W.Het-10, wherein Het is a radical of formula Het-1 a.

In groups (a), (c), (e), (aa), (ca) and (ea) of embodiments the radical R ^w6 is as defined above and in particular selected from the group consisting of hydrogen, halogen, such as fluorine or chlorine, CN, Ci-C4-alkyl, such as methyl, ethyl, n-propyl and isopropyl, C1-C4- haloalkyl, in particular Ci-C2-haloalkyl, such as fluoromethyl, difluoromethyl, trifluoromethyl, 1 ,1 - difluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl or 2,2,2-trifluoroethyl, Ci-C4-alkoxy, such as methoxy, ethoxy, n-propoxy and isopropoxy, and Ci-C4-haloalkoxy, in particular C1-C2- haloalkoxy, such as fluoromethoxy, difluoromethoxy, trifluoromethoxy, 1 ,1 -difluoroethoxy, 2- fluoroethoxy, 2,2-difluoroethoxy or 2,2,2-trifluoroethoxy. In groups (a), (c), (e), (aa), (ca) and (ea) of embodiments the radical R ^w6 is especially hydrogen.

In groups (b), (d), (f), (ba), (da) and (fa) of embodiments the radical R ^w5 is as defined above and in particular selected from the group consisting of hydrogen, halogen, such as fluorine or chlorine, CN, Ci-C4-alkyl, such as methyl, ethyl, n-propyl and isopropyl, C1-C4- haloalkyl, in particular Ci-C2-haloalkyl, such as fluoromethyl, difluoromethyl, trifluoromethyl, 1 ,1 - difluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl or 2,2,2-trifluoroethyl, Ci-C4-alkoxy, such as methoxy, ethoxy, n-propoxy and isopropoxy, and Ci-C4-haloalkoxy, in particular C1-C2- haloalkoxy, such as fluoromethoxy, difluoromethoxy, trifluoromethoxy, 1 ,1 -difluoroethoxy, 2- fluoroethoxy, 2,2-difluoroethoxy or 2,2,2-trifluoroethoxy. In groups (b), (d), (f), (ba), (da) and (fa) of embodiments the radical R ^w5 is especially hydrogen.

In groups (1 ), (2), (3), (A), (B), (1 -A), (2-A), (3-A), ( (a), (b), (c), (d), (e), (f), (aa), (ba), (ca), (da), (ea) and (fa) of embodiments the radicals R ¹ and R ² are, independently from each other, in particular selected from the group consisting of hydrogen, halogen, such as fluorine or chlorine, CN, Ci-C6-alkyl, in particular Ci-C4-alkyl, such as methyl, ethyl, n-propyl or isopropyl, C3-C6- cycloalkyi, such as cyclopropyl or cyclobutyl, Ci-C6-haloalkyl, in particular Ci-C2-haloalkyl, such as fluoromethyl, difluoromethyl, trifluoromethyl, 1 ,1 -difluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl or 2,2,2-trifluoroethyl, or C3-C6-halocycloalkyl such as 1 -fluorocyclopropyl or 2,2- difluorocyclopropyl, or R ¹ and R ² may together be =CR ¹³ R ¹⁴ or R ¹ and R ² form, together with the carbon atom, which they attached to, a 3- to 5-membered saturated carbocyclic ring such as cyclopropyl, cyclobutyl or cyclopentyl.

In groups (1 ), (2), (3), (A), (B), (1 -A), (2-A), (3-A), (a), (b), (c), (d), (e), (f), (aa), (ba), (ca), (da), (ea) and (fa) of embodiments the radicals R ¹ and R ² are, independently from each other, more particularly selected from the group consisting of hydrogen, halogen, cyano, Ci-C3-alkyl, such as methyl, ethyl or isopropyl, or Ci-C3-haloalkyl such as fluoromethyl, difluoromethyl, trifluoromethyl, 1 ,1 -difluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl or 2,2,2-trifluoroethyl, where in particular at least one of the radicals R ¹ and R ² is hydrogen and where especially both R ¹ and R ² are hydrogen.

In the compounds of formula (I), where the moiety of formula (A) is selected from the moieties of formulae W.Het-1 , W.Het-2, W.Het-3, W.Het-4, W.Het-5, W.Het-6, W.Het-7, W.Het- 8, W.Het-9, W.Het-10, W.Het-1 1 and W.Het-12 and likewise in groups (a), (b), (c), (d), (e), (f),

(aa), (ba), (ca), (da), (ea) and (fa) of embodiments, the variables R ¹ , R ² , R ³ , R ⁴ and Y are as defined above and in particular have the preferred meanings.

In the compounds of formula (I), where the moiety of formula (A) is selected from the moieties of formulae W.Het-1 , W.Het-2, W.Het-3, W.Het-4, W.Het-5, W.Het-6, W.Het-7, W.Het- 8, W.Het-9, W.Het-10, W.Het-1 1 and W.Het-12 and likewise in groups (1 ), (2), (3), (A), (B), (1 -

A), (2-A), (3-A), (a), (b), (c), (d), (e), (f), (aa), (ba), (ca), (da), (ea) and (fa) of embodiments, the variables R ¹ , R ² independently of each other or in particular in combination, in particular have the following meanings:

R ¹ and R ² are, independently from each other, selected from the group consisting of hydrogen, halogen, such as fluorine or chlorine, CN, Ci-C6-alkyl, in particular Ci-C4-alkyl, such as methyl, ethyl, n-propyl or isopropyl, C3-C6-cycloalkyl, such as cyclopropyl or cyclobutyl, Ci-C6-haloalkyl, in particular Ci-C2-haloalkyl, such as fluoromethyl, difluoromethyl, trifluoromethyl, 1 ,1 -difluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl or 2,2,2-trifluoroethyl, or C3-C6-halocycloalkyl such as 1 -fluorocyclopropyl or 2,2-difluorocyclopropyl, or R ¹ and R ² may together be =CR ¹³ R ¹⁴ or R ¹ and R ² form, together with the carbon atom, which they attached to, a 3- to 5 membered saturated carbocyclic ring such as cyclopropyl, cyclobutyl or cyclopentyl;

In the compounds of formula (I) and likewise in groups (1 ), (2), (3), (A), (B), (1 -A), (2-A), (3-A), (a), (b), (c), (d), (e), (f), (aa), (ba), (ca), (da), (ea) and (fa) of embodiments, X is in particular O. In the compounds of formula (I), and likewise the compounds of groups (1 ), (2) and (3) embodiments and also of groups (A), (B), (1 -A), (2-A) and (3-A) embodiments, where the moiety of formula (A) is selected from the moieties of formulae W.Het-1 , W.Het-2, W.Het-3, W.Het-4, W.Het-5, W.Het-6, W.Het-7, W.Het-8, W.Het-9, W.Het-10, W.Het-1 1 and W.Het-12 and likewise in groups (1 ), (2), (3), (A), (B), (1 -A), (2-A), (3-A), (a), (b), (c), (d), (e), (f), (aa), (ba), (ca), (da), (ea) and (fa) of embodiments, the variables R ¹ , R ² , independently of each other or in particular in combination, more particularly have the following meanings:

R ¹ and R ² are, independently from each other, selected from the group consisting of hydrogen, halogen, cyano, Ci-C3-alkyl, such as methyl, ethyl or isopropyl, or Ci-C3-haloalkyl such as fluoromethyl, difluoromethyl, trifluoromethyl, 1 ,1 -difluoroethyl, 2-fluoroethyl, 2,2- difluoroethyl or 2,2,2-trifluoroethyl, where in particular at least one of the radicals R ¹ and R ² is hydrogen and where especially both R ¹ and R ² are hydrogen.

Apart from that, the variables Het ^# , R ^v , R ^w , R ⁶ , R ⁷ , R ^7a , R ^7b , R ^7c , R ^7d , R ⁸ , R ⁹ , R ^9a , R ^9b , R ¹⁰ , R ¹¹ , R ¹² , R ¹³ , R ¹⁴ , R ¹⁵ , R ¹⁶ , R ¹⁷ , R ^17a , R ^17b and R ^17c , irrespectively of their occurrence, in particular have the following meanings, if not stated otherwise:

Het ^# in particular represents a 5- or 6-membered saturated, partially unsaturated or unsaturated aromatic heterocyclic ring comprising 1 , 2 or 3 heteroatoms as ring members, which are selected from oxygen, nitrogen and/or sulfur, where the aromatic heterocyclic ring is optionally substituted with 1 , 2 or 3 identical or different substituents R ¹⁰ , and where Het ^# is in particular a 5- or 6-membered aromatic heterocyclic ring, i.e. hetaryl, comprising 1 , 2 or 3 heteroatoms as ring members, which are selected from oxygen, nitrogen and/or sulfur, such as pyridyl, pyrimidinyl, pyrazinyl, pyridazinly, thienyl, furyl, pyrrolyl, oxazolyl, thiazolyl, pyrazolyl, imidazolyl, isothiazolyl or isoxazolyl, where hetaryl is optionally substituted with 1 , 2, 3 or 4 identical or different substituents R ¹⁰ and where the radical R ¹⁰ , irrespective of its occurrence, is in particular selected from halogen, CN, Ci-C4-alkyl, Ci-C4-alkylcarbonyl, Ci-C4-haloalkyl, C1-C4- alkoxy, and Ci-C4-haloalkoxy.

R ^v is hydrogen or together with an R ^v , which is bound to an adjacent carbon atom, forms together with the existing bound a C=C-double bond.

R ^w irrespectively of its occurrence, is selected from the group consisting of hydrogen, halogen, such as fluorine or chlorine, CN, Ci-C4-alkyl, such as methyl, ethyl, n-propyl and isopropyl, Ci-C4-haloalkyl, in particular Ci-C2-haloalkyl, such as fluoromethyl,

difluoromethyl, trifluoromethyl, 1 ,1 -difluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl or 2,2,2- trifluoroethyl, Ci-C4-alkoxy, such as methoxy, ethoxy, n-propoxy and isopropoxy, and C1-C4- haloalkoxy, in particular Ci-C2-haloalkoxy, such as fluoromethoxy, difluoromethoxy, trifluoromethoxy, 1 ,1 -difluoroethoxy, 2-fluoroethoxy, 2,2-difluoroethoxy or 2,2,2-trifluoroethoxy. R ^w is more particularly hydrogen, chlorine, fluorine or methyl and especially hydrogen.

R ⁶ irrespectively of its occurrence, is selected from the group consisting of halogen, such as chlorine or fluorine, Ci-C4-alkyl, such as methyl or ethyl, Ci-C4-alkoxy, such as methoxy or ethoxy, Ci-C4-haloalkoxy, such as difluoromethoxy or trifluormethoxy, and Ci-C4-haloalkyl, such as difluoromethyl, trifluoromethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl or pentafluoroethyl, more preferably from halogen, Ci-C4-alkyl and Ci-C4-haloalkyl, even more preferably from fluorine, chlorine, Ci-C2-alkyl, such as methyl or ethyl and Ci-C2-haloalkyl such as

difluoromethyl, trifluoromethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl or pentafluoroethyl.

R ⁷ irrespectively of its occurrence, is selected from the group consisting of CN, C1-C4- alkoxy, such as methoxy or ethoxy, Ci-C4-haloalkoxy, such as difluoromethoxy or

trifluormethoxy, such as difluoromethyl, trifluoromethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl or pentafluoroethyl, more preferably from halogen, Ci-C4-alkyl and Ci-C4-haloalkyl, even more preferably from fluorine, chlorine, Ci-C2-alkyl, such as methyl or ethyl and Ci-C2-haloalkyl such as difluoromethyl, trifluoromethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl or pentafluoroethyl, C3- C6-cycloalkyl such as cyclopropyl, cyclobutyl or cyclopropyl, and C3-C6-halocycloalkyl.

R ^7a irrespectively of its occurrence, is selected from the group consisting of hydrogen, Ci-C4-alkyl, Ci-C4-haloalkyl, C3-C6-cycloalkyl, C3-C6-cycloalkyl- Ci-C4-alkyl, phenyl and benzyl, where the phenyl ring in the last two radicals is unsubstitued or substituted by 1 , 2 or 3 identical or different radicals selected from the group consisting of halogen, such as chlorine or fluorine, CN, Ci-C4-alkyl, such as methyl, ethyl, n-propyl and isopropyl, C1-C4- haloalkyl, in particular Ci-C2-haloalkyl, such as fluoromethyl, difluoromethyl, trifluoromethyl, 1 ,1 - difluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl or 2,2,2-trifluoroethyl, Ci-C4-alkoxy, such as methoxy, ethoxy, n-propoxy and isopropoxy, and Ci-C4-haloalkoxy, in particular C1-C2- haloalkoxy, such as fluoromethoxy, difluoromethoxy, trifluoromethoxy, 1 ,1 -difluoroethoxy, 2- fluoroethoxy, 2,2-difluoroethoxy or 2,2,2-trifluoroethoxy.

R ^7b is preferably selected from the group consisting of halogen, Ci-C4-alkyl, C1-C4- haloalkyl, C3-C6-cycloalkyl, C3-C6-cycloalkylmethyl, phenyl and benzyl, it being possible for phenyl and benzyl to be unsubstituted, partly or completely halogenated, or two radicals R ^7c bound the same carbon atom may be =0 or =CH2 and where R ^7b is more particularly fluorine, chlorine, Ci-C4-alkyl, such as methyl, ethyl, propyl, isopropyl or n-butyl, Ci-C4-haloalkyl, especially Ci-C2-fluoroalkyl, such as fluoromethyl, difluoromethyl, trifluoromethyl, 1 ,1 - difluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl or 2,2,2-trifluoroethyl.

R ^7c is preferably selected from the group consisting of halogen, Ci-C4-alkyl, C1-C4- haloalkyi, C3-C6-cycloalkyl, C3-C6-cycloalkylmethyl, phenyl and benzyl, it being possible for phenyl and benzyl to be unsubstituted, partly or completely halogenated, or two radicals R ^7c bound the same carbon atom may be =CR ¹³ R ¹⁴ and where R ^7c is more particularly fluorine, Ci- C4-alkyl, such as methyl, ethyl, propyl, isopropyl or n-butyl, Ci-C4-haloalkyl, especially C1-C2- fluoroalkyl, such as fluoromethyl, difluoromethyl, trifluoromethyl, 1 ,1 -difluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl or 2,2,2-trifluoroethyl or two radicals R ^7c bound the same carbon atom may be =CH ₂ .

R ^7d is selected from the group consisting of hydrogen, Ci-C6-alkyl, in particular C1-C4- alkyl, such as methyl, ethyl, n-propyl, isopropyl, n-butyl, 2-butyl, isobutyl or tert. -butyl, C3-C6- cycloalkyl, such as cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl, C3-C6-cycloalkyl-methyl, such as cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyl or cyclohexylmethyl, wherein the carbon atoms of each Ci-C6-alkyl, C3-C6-cycloalkyl and C3-C6-cycloalkylmethyl are unsubstituted, partly or completely halogenated, phenyl and benzyl, wherein phenyl in the last two radicals is unsubstituted or carry 1 , 2 or 3 identical or different radicals R ¹⁰ , which are preferably selected, independently of each other from halogen, CN, Ci-C4-alkyl, Ci-C4-alkoxy, Ci-C4-alkylthio, Ci-C4-haloalkyl, Ci-C4-haloalkoxy and Ci-C4-haloalkyl.

R ⁸ irrespectively of its occurrence, is selected from the group consisting of C1-C4- alkyl, Ci-C4-haloalkyl, C3-C6-cycloalkyl, C3-C6-cycloalkyl- Ci-C4-alkyl, phenyl and benzyl, where the phenyl ring in the last two radicals is unsubstitued or substituted by 1 , 2 or 3 identical or different radicals selected from the group consisting of halogen, such as chlorine or fluorine, CN, Ci-C4-alkyl, such as methyl, ethyl, n-propyl and isopropyl, Ci-C4-haloalkyl, in particular Ci- C2-haloalkyl, such as fluoromethyl, difluoromethyl, trifluoromethyl, 1 ,1 -difluoroethyl, 2- fluoroethyl, 2,2-difluoroethyl or 2,2,2-trifluoroethyl, Ci-C4-alkoxy, such as methoxy, ethoxy, n- propoxy and isopropoxy, and Ci-C4-haloalkoxy, in particular Ci-C2-haloalkoxy, such as fluoromethoxy, difluoromethoxy, trifluoromethoxy, 1 ,1 -difluoroethoxy, 2-fluoroethoxy, 2,2- difluoroethoxy or 2,2,2-trifluoroethoxy.

R ⁹ irrespectively of its occurrence, is selected from the group consisting of C1-C4- alkyl, Ci-C4-haloalkyl, C3-C6-cycloalkyl, C3-C6-cycloalkyl-Ci-C4-alkyl, phenyl and benzyl, where the phenyl ring in the last two radicals is unsubstitued or substituted by 1 , 2 or 3 identical or different radicals selected from the group consisting of halogen, such as chlorine or fluorine, CN, Ci-C4-alkyl, such as methyl, ethyl, n-propyl and isopropyl, Ci-C4-haloalkyl, in particular Ci- C2-haloalkyl, such as fluoromethyl, difluoromethyl, trifluoromethyl, 1 ,1 -difluoroethyl, 2- fluoroethyl, 2,2-difluoroethyl or 2,2,2-trifluoroethyl, Ci-C4-alkoxy, such as methoxy, ethoxy, n- propoxy and isopropoxy, and Ci-C4-haloalkoxy, in particular Ci-C2-haloalkoxy, such as fluoromethoxy, difluoromethoxy, trifluoromethoxy, 1 ,1 -difluoroethoxy, 2-fluoroethoxy, 2,2- difluoroethoxy or 2,2,2-trifluoroethoxy. R ^9a and R ^9b irrespectively of their occurrence, are preferably selected from the group consisting of hydrogen, Ci-C4-alkyl, such as methyl, ethyl, n-propyl, isopropyl, n-butyl, 2-butyl or isobutyl, and Ci-C4-haloalkyl, such as fluoromethyl, difluoromethyl, trifluoromethyl, 1 ,1 - difluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl or 2,2,2-trifluoroethyl, or NR ^9a R ^9b may also be a saturated N-bound 3-, 4-, 5- or 6-membered heterocycle, which in addition to the nitrogen atom may have 1 further heteroatom as ring members, which is selected from O and N and where the N-bound 3-, 4-, 5- or 6-membered heterocycle may be unsubstituted or carry 1 , 2, 3 or 4 radicals selected from Ci-C4-alkyl and Ci-C4-haloalkyl. Examples of such radicals NR ^9a R ^9b include, but are not limited to methylamino, ethylamino, n-propylamino, isopropylamino, n- butylamino, 2-butylamino, isobutylamino, dimethylamino, diethylamino, di-n-propylamino, di-n- butylamino, N-methyl-N-ethylamino, N-methyl-N-propylamino, N-methyl-N-n-propylamino, N- methyl-N-isopropylamino, N-methyl-N-n-butylamino, N-methyl-N-2-butylamino, N-methyl-N- isobutylamino, 1 -pyrrolidinyl, 1 -piperidinyl, 1 -piperazinly, 4-methyl-1 -piperazinly and 4- morpholinyl.

R ¹⁰ irrespectively of its occurrence, is selected from the group consisting of halogen, such as chlorine or fluorine, CN, Ci-C4-alkyl, such as methyl, ethyl, n-propyl and isopropyl, Ci- C4-haloalkyl, in particular Ci-C2-haloalkyl, such as fluoromethyl, difluoromethyl, trifluoromethyl, 1 ,1 -difluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl or 2,2,2-trifluoroethyl, Ci-C4-alkoxy, such as methoxy, ethoxy, n-propoxy and isopropoxy, and Ci-C4-haloalkoxy, in particular C1-C2- haloalkoxy, such as fluoromethoxy, difluoromethoxy, trifluoromethoxy, 1 ,1 -difluoroethoxy, 2- fluoroethoxy, 2,2-difluoroethoxy or 2,2,2-trifluoroethoxy.

R ¹¹ , R ¹² independently of their occurrence, are selected from the group consisting of Ci- C6-alkyl, Ci-C6-alkoxy, Cs-Cs-cycloalkyl, C3-C8-cycloalkyl-Ci-C4-alkyl, phenyl and benzyl, where the phenyl ring in last two radicals are unsubstituted or substituted with 1 , 2, or 3 identical or different radicals selected from fluorine, chlorine, Ci-C3-alkyl, Ci-C2-haloalkyl, Ci-C2-alkoxy and Ci-C2-haloalkoxy.

R ¹³ , R ¹⁴ independently of their occurrence, are selected from the group consisting of hydrogen, fluorine, chlorine, CN, Ci-C4-alkyl, such as methyl, ethyl, n-propyl or n-butyl, C3-C6- cycloalkyl, such as cyclopropyl, cyclobutyl or cyclopentyl, and phenyl.

R ¹⁵ irrespectively of its occurrence, is selected from the group consisting of hydrogen, Ci-C4-alkyl, Ci-C4-haloalkyl, C3-C6-cycloalkyl, C3-C6-cycloalkyl- Ci-C4-alkyl, phenyl and benzyl, where the phenyl ring in the last two radicals is unsubstitued or substituted by 1 , 2 or 3 identical or different radicals selected from the group consisting of halogen, such as chlorine or fluorine, CN, Ci-C4-alkyl, such as methyl, ethyl, n-propyl and isopropyl, C1-C4- haloalkyl, in particular Ci-C2-haloalkyl, such as fluoromethyl, difluoromethyl, trifluoromethyl, 1 ,1 - difluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl or 2,2,2-trifluoroethyl, Ci-C4-alkoxy, such as methoxy, ethoxy, n-propoxy and isopropoxy, and Ci-C4-haloalkoxy, in particular C1-C2- haloalkoxy, such as fluoromethoxy, difluoromethoxy, trifluoromethoxy, 1 ,1-difluoroethoxy, 2- fluoroethoxy, 2,2-difluoroethoxy or 2,2,2-trifluoroethoxy.

R ¹⁶ irrespectively of its occurrence, is selected from the group consisting of C1-C4- alkyl, Ci-C4-haloalkyl, C3-C6-cycloalkyl, C3-C6-cycloalkyl-Ci-C4-alkyl, phenyl and benzyl, where the phenyl ring in the last two radicals is unsubstitued or substituted by 1 , 2 or 3 identical or different radicals selected from the group consisting of halogen, such as chlorine or fluorine, CN, Ci-C4-alkyl, such as methyl, ethyl, n-propyl and isopropyl, Ci-C4-haloalkyl, in particular Ci- C2-haloalkyl, such as fluoromethyl, difluoromethyl, trifluoromethyl, 1 ,1 -difluoroethyl, 2- fluoroethyl, 2,2-difluoroethyl or 2,2,2-trifluoroethyl, Ci-C4-alkoxy, such as methoxy, ethoxy, n- propoxy and isopropoxy, and Ci-C4-haloalkoxy, in particular Ci-C2-haloalkoxy, such as fluoromethoxy, difluoromethoxy, trifluoromethoxy, 1 ,1-difluoroethoxy, 2-fluoroethoxy, 2,2- difluoroethoxy or 2,2,2-trifluoroethoxy.

R ¹⁷ irrespectively of its occurrence, is selected from the group consisting of hydrogen, Ci-C6-alkyl, Ci-C4-haloalkyl, Ci-C6-alkoxy, Ci-C4-haloalkoxy, C3-C6-alkenyl, C3-C6- cycloalkyl-Ci-C4-alkyl, phenyl and benzyl, where the phenyl ring in the last two radicals is unsubstitued or substituted by 1 , 2 or 3 identical or different radicals selected from the group consisting of halogen, such as chlorine or fluorine, CN, Ci-C4-alkyl, such as methyl, ethyl, n- propyl and isopropyl, Ci-C4-haloalkyl, in particular Ci-C2-haloalkyl, such as fluoromethyl, difluoromethyl, trifluoromethyl, 1 ,1 -difluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl or 2,2,2- trifluoroethyl, Ci-C4-alkoxy, such as methoxy, ethoxy, n-propoxy and isopropoxy, and C1-C4- haloalkoxy, in particular Ci-C2-haloalkoxy, such as fluoromethoxy, difluoromethoxy,

trifluoromethoxy, 1 ,1-difluoroethoxy, 2-fluoroethoxy, 2,2-difluoroethoxy or 2,2,2-trifluoroethoxy.

R ^17a and R ^17b irrespectively of their occurrence, are preferably selected from the group consisting of hydrogen, Ci-C4-alkyl, such as methyl, ethyl, n-propyl, isopropyl, n-butyl, 2-butyl or isobutyl, and Ci-C4-haloalkyl, such as fluoromethyl, difluoromethyl, trifluoromethyl, 1 ,1- difluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl or 2,2,2-trifluoroethyl, or NR ^9a R ^9b may also be a saturated N-bound 3-, 4-, 5- or 6-membered heterocycle, which in addition to the nitrogen atom may have 1 further heteroatom as ring members, which is selected from O and N and where the N-bound 3-, 4-, 5- or 6-membered heterocycle may be unsubstituted or carry 1 , 2, 3 or 4 radicals selected from Ci-C4-alkyl and Ci-C4-haloalkyl. Examples of such radicals NR ^9a R ^9b include, but are not limited to methylamino, ethylamino, n-propylamino, isopropylamino, n- butylamino, 2-butylamino, isobutylamino, dimethylamino, diethylamino, di-n-propylamino, di-n- butylamino, N-methyl-N-ethylamino, N-methyl-N-propylamino, N-methyl-N-n-propylamino, N- methyl-N-isopropylamino, N-methyl-N-n-butylamino, N-methyl-N-2-butylamino, N-methyl-N- isobutylamino, 1 -pyrrolidinyl, 1 -piperidinyl, 1 -piperazinly, 4-methyl-1 -piperazinly and 4- morpholinyl.

R ^17c irrespectively of its occurrence, is selected from the group consisting of hydrogen, Ci-C4-alkyl, Ci-C4-haloalkyl, C3-C6-cycloalkyl, C3-C6-cycloalkyl- Ci-C4-alkyl, phenyl and benzyl, where the phenyl ring in the last two radicals is unsubstitued or substituted by 1 , 2 or 3 identical or different radicals selected from the group consisting of halogen, such as chlorine or fluorine, CN, Ci-C4-alkyl, such as methyl, ethyl, n-propyl and isopropyl, C1-C4- haloalkyl, in particular Ci-C2-haloalkyl, such as fluoromethyl, difluoromethyl, trifluoromethyl, 1 ,1 - difluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl or 2,2,2-trifluoroethyl, Ci-C4-alkoxy, such as methoxy, ethoxy, n-propoxy and isopropoxy, and Ci-C4-haloalkoxy, in particular C1-C2- haloalkoxy, such as fluoromethoxy, difluoromethoxy, trifluoromethoxy, 1 ,1 -difluoroethoxy, 2- fluoroethoxy, 2,2-difluoroethoxy or 2,2,2-trifluoroethoxy.

A special group of embodiments relates to the compounds of formula (l)-A.1 a, to their tautomers, to their stereoisomers and to their salts, where R ¹ , D, Y, R ³ and R ⁴ are as defined above and where R ¹ , D, Y, R ³ and R ⁴ have in particular one of the meanings given in any of lines 1 to 1080 of the following table A. Further examples of this special group of embodiments are the compounds of formula (l)-A.1 a, their tautomers, their stereoisomers and their salts, where R ¹ is CH3 and where D, Y, R ³ and R ⁴ have one of the meanings given in any of lines 1 to 1080 of the following table A.

A further special group of embodiments relates to the compounds of formula (l)-A.2a, to their tautomers, to their stereoisomers and to their salts, where R ¹ , D, Y, R ³ and R ⁴ are as defined above and where R ¹ , D, Y, R ³ and R ⁴ have in particular one of the meanings given in any of lines 1 to 1080 of the following table A. Further examples of this special group of embodiments are the compounds of formula (l)-A.2a, their tautomers, their stereoisomers and their salts, where R ¹ is CH3 and where D, Y, R ³ and R ⁴ have one of the meanings given in any of lines 1 to 1080 of the following table A.

A further special group of embodiments relates to the compounds of formula (l)-A.1 b, to their tautomers, to their stereoisomers and to their salts, where R ¹ , D, Y, R ³ and R ⁴ are as defined above and where R ¹ , D, Y, R ³ and R ⁴ have in particular one of the meanings given in any of lines 1 to 1080 of the following table A. Further examples of this special group of embodiments are the compounds of formula (l)-A.1 b, their tautomers, their stereoisomers and their salts, where R ¹ is CH3 and where D, Y, R ³ and R ⁴ have one of the meanings given in any of lines 1 to 1080 of the following table A. A further special group of embodiments relates to the compounds of formula (l)-A.2b, to their tautomers, to their stereoisomers and to their salts, where R ¹ , D, Y, R ³ and R ⁴ are as defined above and where R ¹ , D, Y, R ³ and R ⁴ have in particular one of the meanings given in any of lines 1 to 1080 of the following table A. Further examples of this special group of embodiments are the compounds of formula (l)-A.2b, their tautomers, their stereoisomers and their salts, where R ¹ is CH3 and where D, Y, R ³ and R ⁴ have one of the meanings given in any of lines 1 to 1080 of the following table A.

A further special group of embodiments relates to the compounds of formula (l)-A.1 c, to their tautomers, to their stereoisomers and to their salts, where R ¹ , D, Y, R ³ and R ⁴ are as defined above and where R ¹ , D, Y, R ³ and R ⁴ have in particular one of the meanings given in any of lines 1 to 1080 of the following table A. Further examples of this special group of embodiments are the compounds of formula (l)-A.1 c, their tautomers, their stereoisomers and their salts, where R ¹ is CH3 and where D, Y, R ³ and R ⁴ have one of the meanings given in any of lines 1 to 1080 of the following table A.

A further special group of embodiments relates to the compounds of formula (l)-A.2c, to their tautomers, to their stereoisomers and to their salts, where R ¹ , D, Y, R ³ and R ⁴ are as defined above and where R ¹ , D, Y, R ³ and R ⁴ have in particular one of the meanings given in any of lines 1 to 1080 of the following table A. Further examples of this special group of embodiments are the compounds of formula (l)-A.2c, their tautomers, their stereoisomers and their salts, where R ¹ is CH3 and where D, Y, R ³ and R ⁴ have one of the meanings given in any of lines 1 to 1080 of the following table A.

A further special group of embodiments relates to the compounds of formula (l)-A.1 d, to their tautomers, to their stereoisomers and to their salts, where R ¹ , D, Y, R ³ and R ⁴ are as defined above and where R ¹ , D, Y, R ³ and R ⁴ have in particular one of the meanings given in any of lines 1 to 1080 of the following table A. Further examples of this special group of embodiments are the compounds of formula (l)-A.1 d, their tautomers, their stereoisomers and their salts, where R ¹ is CH3 and where D, Y, R ³ and R ⁴ have one of the meanings given in any of lines 1 to 1080 of the following table A.

A further special group of embodiments relates to the compounds of formula (l)-A.2d, to their tautomers, to their stereoisomers and to their salts, where R ¹ , D, Y, R ³ and R ⁴ are as defined above and where R ¹ , D, Y, R ³ and R ⁴ have in particular one of the meanings given in any of lines 1 to 1080 of the following table A. Further examples of this special group of embodiments are the compounds of formula (l)-A.2d, their tautomers, their stereoisomers and their salts, where R ¹ is CH3 and where D, Y, R ³ and R ⁴ have one of the meanings given in any of lines 1 to 1080 of the following table A. A further special group of embodiments relates to the compounds of formula (l)-A.3a, to their tautomers, to their stereoisomers and to their salts, where R ¹ , D, Y, R ³ and R ⁴ are as defined above and where R ¹ , D, Y, R ³ and R ⁴ have in particular one of the meanings given in any of lines 1 to 1080 of the following table A. Further examples of this special group of embodiments are the compounds of formula (l)-A.3a, their tautomers, their stereoisomers and their salts, where R ¹ is CH3 and where D, Y, R ³ and R ⁴ have one of the meanings given in any of lines 1 to 1080 of the following table A.

A further special group of embodiments relates to the compounds of formula (l)-A.4a, to their tautomers, to their stereoisomers and to their salts, where R ¹ , D, Y, R ³ and R ⁴ are as defined above and where R ¹ , D, Y, R ³ and R ⁴ have in particular one of the meanings given in any of lines 1 to 1080 of the following table A. Further examples of this special group of embodiments are the compounds of formula (l)-A.4a, their tautomers, their stereoisomers and their salts, where R ¹ is CH3 and where D, Y, R ³ and R ⁴ have one of the meanings given in any of lines 1 to 1080 of the following table A.

A further special group of embodiments relates to the compounds of formula (l)-A.3b, to their tautomers, to their stereoisomers and to their salts, where R ¹ , D, Y, R ³ and R ⁴ are as defined above and where R ¹ , D, Y, R ³ and R ⁴ have in particular one of the meanings given in any of lines 1 to 1080 of the following table A. Further examples of this special group of embodiments are the compounds of formula (l)-A.3b, their tautomers, their stereoisomers and their salts, where R ¹ is CH3 and where D, Y, R ³ and R ⁴ have one of the meanings given in any of lines 1 to 1080 of the following table A.

A further special group of embodiments relates to the compounds of formula (l)-A.4b, to their tautomers, to their stereoisomers and to their salts, where R ¹ , D, Y, R ³ and R ⁴ are as defined above and where R ¹ , D, Y, R ³ and R ⁴ have in particular one of the meanings given in any of lines 1 to 1080 of the following table A. Further examples of this special group of embodiments are the compounds of formula (l)-A.4b, their tautomers, their stereoisomers and their salts, where R ¹ is CH3 and where D, Y, R ³ and R ⁴ have one of the meanings given in any of lines 1 to 1080 of the following table A.

A further special group of embodiments relates to the compounds of formula (l)-A.3c, to their tautomers, to their stereoisomers and to their salts, where R ¹ , D, Y, R ³ and R ⁴ are as defined above and where R ¹ , D, Y, R ³ and R ⁴ have in particular one of the meanings given in any of lines 1 to 1080 of the following table A. Further examples of this special group of embodiments are the compounds of formula (l)-A.3c, their tautomers, their stereoisomers and their salts, where R ¹ is CH3 and where D, Y, R ³ and R ⁴ have one of the meanings given in any of lines 1 to 1080 of the following table A. A further special group of embodiments relates to the compounds of formula (l)-A.4c, to their tautomers, to their stereoisomers and to their salts, where R ¹ , D, Y, R ³ and R ⁴ are as defined above and where R ¹ , D, Y, R ³ and R ⁴ have in particular one of the meanings given in any of lines 1 to 1080 of the following table A. Further examples of this special group of embodiments are the compounds of formula (l)-A.4c, their tautomers, their stereoisomers and their salts, where R ¹ is CH3 and where D, Y, R ³ and R ⁴ have one of the meanings given in any of lines 1 to 1080 of the following table A.

A further special group of embodiments relates to the compounds of formula (l)-A.3d, to their tautomers, to their stereoisomers and to their salts, where R ¹ , D, Y, R ³ and R ⁴ are as defined above and where R ¹ , D, Y, R ³ and R ⁴ have in particular one of the meanings given in any of lines 1 to 1080 of the following table A. Further examples of this special group of embodiments are the compounds of formula (l)-A.3d, their tautomers, their stereoisomers and their salts, where R ¹ is CH3 and where D, Y, R ³ and R ⁴ have one of the meanings given in any of lines 1 to 1080 of the following table A.

A further special group of embodiments relates to the compounds of formula (l)-A.4d, to their tautomers, to their stereoisomers and to their salts, where R ¹ , D, Y, R ³ and R ⁴ are as defined above and where R ¹ , D, Y, R ³ and R ⁴ have in particular one of the meanings given in any of lines 1 to 1080 of the following table A. Further examples of this special group of embodiments are the compounds of formula (l)-A.4d, their tautomers, their stereoisomers and their salts, where R ¹ is CH3 and where D, Y, R ³ and R ⁴ have one of the meanings given in any of lines 1 to 1080 of the following table A.

A skilled person will readily appreciate that the compounds of formulae (l)-A.1 a, (l)-A.2a, (l)-A.3a, (l)-A.4a, (l)-A.1 b, (l)-A.2b, (l)-A.3b, (l)-A.4b, (l)-A.1 c, (l)-A.2c, (l)-A.3c, (l)-A.4c, (l)-A.1 d, (l)-A.2d, (l)-A.3d and (l)-A.4d, where R ¹ is methyl and D, Y, R ³ and R ⁴ have the meanings given in one of lines 1 to 1080 of the following table A may have R- or S-configuration with regard to the carbon atom that carries R ¹ . The aforementioned embodiments include both the R-isomer a

l-A.1 a l-A.2a

I-A.3a l-A.4a

I-A.3d l-A.4d Table A:

R D Y R ³ R ⁴

1 H CH ₂ 0 H H

2 H CH ₂ 0 CHs H

3 H CH ₂ 0 CH ₂ CHs H

4 H CH ₂ 0 CH(CHs) ₂ H

5 H CH ₂ 0 CHs CHs

6 H CH ₂ 0 CH ₂ CHs CHs

7 H CH ₂ 0 CH(CHs) ₂ CHs

R D Y R ³ R ⁴

74 H CH ₂ N(CH ₃ ) SCH ₃ H

75 H CH ₂ N(CH ₃ ) SCH ₃ CH ₃

76 H CH ₂ N(CH ₃ ) SCH ₃ CH ₂ CH ₃

77 H CH ₂ N(CH ₃ ) SCH ₃ CH(CH ₃ ) ₂

78 H CH ₂ N(CH ₃ ) OCH ₂ CH ₃ OCH ₂ CH ₃

79 H CH ₂ N(CH ₃ ) OCH ₂ CH ₃ H

80 H CH ₂ N(CH ₃ ) OCH ₂ CH ₃ CH ₃

81 H CH ₂ N(CH ₃ ) OCH ₂ CH ₃ CH ₂ CH ₃

82 H CH ₂ N(CH ₃ ) OCH ₂ CH ₃ CH(CH ₃ ) ₂

83 H CH ₂ N(CH ₃ ) -CH ₂ -CH ₂ -CH ₂ -

84 H CH ₂ N(CH ₃ ) -CH ₂ -CH ₂ -CH ₂ -CH ₂ -

85 H CH ₂ N(CH ₃ ) -CH ₂ -CH ₂ -CH ₂ -CH ₂ -CH ₂ -

86 H CH ₂ N(CH ₃ ) -S-CH=CH-S-

87 H CH ₂ N(CH ₃ ) -S-CH ₂ -CH ₂ -S-

88 H CH ₂ N(CH ₃ ) -S-CH ₂ -CH ₂ -CH ₂ -S-

89 H CH ₂ N(CH ₃ ) -NH-CH ₂ -CH ₂ -NH-

90 H CH ₂ N(CH ₃ ) -N(CH ₃ )-CH ₂ -CH ₂ -N(CH ₃ )-

91 H CH ₂ N-C(=0)-CH ₃ H H

92 H CH ₂ N-C(=0)-CH ₃ CH ₃ H

93 H CH ₂ N-C(=0)-CH ₃ CH ₂ CH ₃ H

94 H CH ₂ N-C(=0)-CH ₃ CH(CH ₃ ) ₂ H

95 H CH ₂ N-C(=0)-CH ₃ CH ₃ CH ₃

96 H CH ₂ N-C(=0)-CH ₃ CH ₂ CH ₃ CH ₃

97 H CH ₂ N-C(=0)-CH ₃ CH(CH ₃ ) ₂ CH ₃

98 H CH ₂ N-C(=0)-CH ₃ CH ₂ CH ₃ CH ₂ CH ₃

99 H CH ₂ N-C(=0)-CH ₃ CH(CH ₃ ) ₂ CH ₂ CH ₃

100 H CH ₂ N-C(=0)-CH ₃ CH(CH ₃ ) ₂ CH(CH ₃ ) ₂

101 H CH ₂ N-C(=0)-CH ₃ H

102 H CH ₂ N-C(=0)-CH ₃ 4-CI-C ₆ H ₄ H

103 H CH ₂ N-C(=0)-CH ₃ SCH ₃ SCH ₃

104 H CH ₂ N-C(=0)-CH ₃ SCH ₃ H

105 H CH ₂ N-C(=0)-CH ₃ SCH ₃ CH ₃

106 H CH ₂ N-C(=0)-CH ₃ SCH ₃ CH ₂ CH ₃ R D Y R ³ R ⁴

107 H CH ₂ N-C(=0)-CH ₃ SCH ₃ CH(CH ₃ ) ₂

108 H CH ₂ N-C(=0)-CH ₃ OCH ₂ CH ₃ OCH ₂ CH ₃

109 H CH ₂ N-C(=0)-CH ₃ OCH ₂ CH ₃ H

110 H CH ₂ N-C(=0)-CH ₃ OCH ₂ CH ₃ CH ₃

11 1 H CH ₂ N-C(=0)-CH ₃ OCH ₂ CH ₃ CH ₂ CH ₃

112 H CH ₂ N-C(=0)-CH ₃ OCH ₂ CH ₃ CH(CH ₃ ) ₂

113 H CH ₂ N-C(=0)-CH ₃ -CH ₂ -CH ₂ -CH ₂ -

114 H CH ₂ N-C(=0)-CH ₃ -CH ₂ -CH ₂ -CH ₂ -CH ₂ -

115 H CH ₂ N-C(=0)-CH ₃ -CH ₂ -CH ₂ -CH ₂ -CH ₂ -CH ₂ -

116 H CH ₂ N-C(=0)-CH ₃ -S-CH=CH-S-

117 H CH ₂ N-C(=0)-CH ₃ -S-CH ₂ -CH ₂ -S-

118 H CH ₂ N-C(=0)-CH ₃ -S-CH ₂ -CH ₂ -CH ₂ -S-

119 H CH ₂ N-C(=0)-CH ₃ -NH-CH ₂ -CH ₂ -NH-

120 H CH ₂ N-C(=0)-CH ₃ -N(CH ₃ )-CH ₂ -CH ₂ -N(CH ₃ )-

121 H CF ₂ 0 H H

122 H CF ₂ 0 CH ₃ H

123 H CF ₂ 0 CH ₂ CH ₃ H

124 H CF ₂ 0 CH(CH ₃ ) ₂ H

125 H CF ₂ 0 CH ₃ CH ₃

126 H CF ₂ 0 CH ₂ CH ₃ CH ₃

127 H CF ₂ 0 CH(CH ₃ ) ₂ CH ₃

128 H CF ₂ 0 CH ₂ CH ₃ CH ₂ CH ₃

129 H CF ₂ 0 CH(CH ₃ ) ₂ CH ₂ CH ₃

130 H CF ₂ 0 CH(CH ₃ ) ₂ CH(CH ₃ ) ₂

131 H CF ₂ 0 H

132 H CF ₂ 0 4-CI-C ₆ H ₄ H

133 H CF ₂ 0 SCH ₃ SCH ₃

134 H CF ₂ 0 SCH ₃ H

135 H CF ₂ 0 SCH ₃ CH ₃

136 H CF ₂ 0 SCH ₃ CH ₂ CH ₃

137 H CF ₂ 0 SCH ₃ CH(CH ₃ ) ₂

138 H CF ₂ 0 OCH ₂ CH ₃ OCH ₂ CH ₃

139 H CF ₂ 0 OCH ₂ CH ₃ H

R D Y R ³ R ⁴

206 H CF ₂ N(CH ₃ ) -S-CH=CH-S-

207 H CF ₂ N(CH ₃ ) -S-CH ₂ -CH ₂ -S-

208 H CF ₂ N(CH ₃ ) -S-CH ₂ -CH ₂ -CH ₂ -S-

209 H CF ₂ N(CH ₃ ) -NH-CH ₂ -CH ₂ -NH-

210 H CF ₂ N(CH ₃ ) -N(CH ₃ )-CH ₂ -CH ₂ -N(CH ₃ )-

21 1 H CF ₂ N-C(=0)-CH ₃ H H

212 H CF ₂ N-C(=0)-CH ₃ CH ₃ H

213 H CF ₂ N-C(=0)-CH ₃ CH ₂ CH ₃ H

214 H CF ₂ N-C(=0)-CH ₃ CH(CH ₃ ) ₂ H

215 H CF ₂ N-C(=0)-CH ₃ CH ₃ CH ₃

216 H CF ₂ N-C(=0)-CH ₃ CH ₂ CH ₃ CH ₃

217 H CF ₂ N-C(=0)-CH ₃ CH(CH ₃ ) ₂ CH ₃

218 H CF ₂ N-C(=0)-CH ₃ CH ₂ CH ₃ CH ₂ CH ₃

219 H CF ₂ N-C(=0)-CH ₃ CH(CH ₃ ) ₂ CH ₂ CH ₃

220 H CF ₂ N-C(=0)-CH ₃ CH(CH ₃ ) ₂ CH(CH ₃ ) ₂

221 H CF ₂ N-C(=0)-CH ₃ H

222 H CF ₂ N-C(=0)-CH ₃ 4-CI-C ₆ H ₄ H

223 H CF ₂ N-C(=0)-CH ₃ SCH ₃ SCH ₃

224 H CF ₂ N-C(=0)-CH ₃ SCH ₃ H

225 H CF ₂ N-C(=0)-CH ₃ SCH ₃ CH ₃

226 H CF ₂ N-C(=0)-CH ₃ SCH ₃ CH ₂ CH ₃

227 H CF ₂ N-C(=0)-CH ₃ SCH ₃ CH(CH ₃ ) ₂

228 H CF ₂ N-C(=0)-CH ₃ OCH ₂ CH ₃ OCH ₂ CH ₃

229 H CF ₂ N-C(=0)-CH ₃ OCH ₂ CH ₃ H

230 H CF ₂ N-C(=0)-CH ₃ OCH ₂ CH ₃ CH ₃

231 H CF ₂ N-C(=0)-CH ₃ OCH ₂ CH ₃ CH ₂ CH ₃

232 H CF ₂ N-C(=0)-CH ₃ OCH ₂ CH ₃ CH(CH ₃ ) ₂

233 H CF ₂ N-C(=0)-CH ₃ -CH ₂ -CH ₂ -CH ₂ -

234 H CF ₂ N-C(=0)-CH ₃ -CH ₂ -CH ₂ -CH ₂ -CH ₂ -

235 H CF ₂ N-C(=0)-CH ₃ -CH ₂ -CH ₂ -CH ₂ -CH ₂ -CH ₂ -

236 H CF ₂ N-C(=0)-CH ₃ -S-CH=CH-S-

237 H CF ₂ N-C(=0)-CH ₃ -S-CH ₂ -CH ₂ -S-

238 H CF ₂ N-C(=0)-CH ₃ -S-CH ₂ -CH ₂ -CH ₂ -S-

R D Y R ³ R ⁴

338 H CH-CN N-C(=0)-CH ₃ CH ₂ CH ₃ CH ₂ CH ₃

339 H CH-CN N-C(=0)-CH ₃ CH(CH ₃ ) ₂ CH ₂ CH ₃

340 H CH-CN N-C(=0)-CH ₃ CH(CH ₃ ) ₂ CH(CH ₃ ) ₂

341 H CH-CN N-C(=0)-CH ₃ C6H5 H

342 H CH-CN N-C(=0)-CH ₃ 4-CI-C ₆ H ₄ H

343 H CH-CN N-C(=0)-CH ₃ SCH ₃ SCH ₃

344 H CH-CN N-C(=0)-CH ₃ SCH ₃ H

345 H CH-CN N-C(=0)-CH ₃ SCH ₃ CH ₃

346 H CH-CN N-C(=0)-CH ₃ SCH ₃ CH ₂ CH ₃

347 H CH-CN N-C(=0)-CH ₃ SCH ₃ CH(CH ₃ ) ₂

348 H CH-CN N-C(=0)-CH ₃ OCH ₂ CH ₃ OCH ₂ CH ₃

349 H CH-CN N-C(=0)-CH ₃ OCH ₂ CH ₃ H

350 H CH-CN N-C(=0)-CH ₃ OCH ₂ CH ₃ CH ₃

351 H CH-CN N-C(=0)-CH ₃ OCH ₂ CH ₃ CH ₂ CH ₃

352 H CH-CN N-C(=0)-CH ₃ OCH ₂ CH ₃ CH(CH ₃ ) ₂

353 H CH-CN N-C(=0)-CH ₃ -CH ₂ -CH ₂ -CH ₂ -

354 H CH-CN N-C(=0)-CH ₃ -CH ₂ -CH ₂ -CH ₂ -CH ₂ -

355 H CH-CN N-C(=0)-CH ₃ -CH ₂ -CH ₂ -CH ₂ -CH ₂ -CH ₂ -

356 H CH-CN N-C(=0)-CH ₃ -S-CH=CH-S-

357 H CH-CN N-C(=0)-CH ₃ -S-CH ₂ -CH ₂ -S-

358 H CH-CN N-C(=0)-CH ₃ -S-CH ₂ -CH ₂ -CH ₂ -S-

359 H CH-CN N-C(=0)-CH ₃ -NH-CH ₂ -CH ₂ -NH-

360 H CH-CN N-C(=0)-CH ₃ -N(CH ₃ )-CH ₂ -CH ₂ -N(CH ₃ )-

361 H CH(CH ₃ ) 0 H H

362 H CH(CH ₃ ) 0 CH ₃ H

363 H CH(CH ₃ ) 0 CH ₂ CH ₃ H

364 H CH(CH ₃ ) 0 CH(CH ₃ ) ₂ H

365 H CH(CH ₃ ) 0 CH ₃ CH ₃

366 H CH(CH ₃ ) 0 CH ₂ CH ₃ CH ₃

367 H CH(CH ₃ ) 0 CH(CH ₃ ) ₂ CH ₃

368 H CH(CH ₃ ) 0 CH ₂ CH ₃ CH ₂ CH ₃

369 H CH(CH ₃ ) 0 CH(CH ₃ ) ₂ CH ₂ CH ₃

370 H CH(CH ₃ ) 0 CH(CH ₃ ) ₂ CH(CH ₃ ) ₂

R D Y R ³ R ⁴

404 H CH(CH ₃ ) NH SCH ₃ H

405 H CH(CH ₃ ) NH SCH ₃ CH ₃

406 H CH(CH ₃ ) NH SCH ₃ CH ₂ CH ₃

407 H CH(CH ₃ ) NH SCH ₃ CH(CH ₃ ) ₂

408 H CH(CH ₃ ) NH OCH ₂ CH ₃ OCH ₂ CH ₃

409 H CH(CH ₃ ) NH OCH ₂ CH ₃ H

410 H CH(CH ₃ ) NH OCH ₂ CH ₃ CH ₃

41 1 H CH(CH ₃ ) NH OCH ₂ CH ₃ CH ₂ CH ₃

412 H CH(CH ₃ ) NH OCH ₂ CH ₃ CH(CH ₃ ) ₂

413 H CH(CH ₃ ) NH -CH ₂ -CH ₂ -CH ₂ -

414 H CH(CH ₃ ) NH -CH ₂ -CH ₂ -CH ₂ -CH ₂ -

415 H CH(CH ₃ ) NH -CH ₂ -CH ₂ -CH ₂ -CH ₂ -CH ₂ -

416 H CH(CH ₃ ) NH -S-CH=CH-S-

417 H CH(CH ₃ ) NH -S-CH ₂ -CH ₂ -S-

418 H CH(CH ₃ ) NH -S-CH ₂ -CH ₂ -CH ₂ -S-

419 H CH(CH ₃ ) NH -NH-CH ₂ -CH ₂ -NH-

420 H CH(CH ₃ ) NH -N(CH ₃ )-CH ₂ -CH ₂ -N(CH ₃ )-

421 H CH(CH ₃ ) N(CH ₃ ) H H

422 H CH(CH ₃ ) N(CH ₃ ) CH ₃ H

423 H CH(CH ₃ ) N(CH ₃ ) CH ₂ CH ₃ H

424 H CH(CH ₃ ) N(CH ₃ ) CH(CH ₃ ) ₂ H

425 H CH(CH ₃ ) N(CH ₃ ) CH ₃ CH ₃

426 H CH(CH ₃ ) N(CH ₃ ) CH ₂ CH ₃ CH ₃

427 H CH(CH ₃ ) N(CH ₃ ) CH(CH ₃ ) ₂ CH ₃

428 H CH(CH ₃ ) N(CH ₃ ) CH ₂ CH ₃ CH ₂ CH ₃

429 H CH(CH ₃ ) N(CH ₃ ) CH(CH ₃ ) ₂ CH ₂ CH ₃

430 H CH(CH ₃ ) N(CH ₃ ) CH(CH ₃ ) ₂ CH(CH ₃ ) ₂

431 H CH(CH ₃ ) N(CH ₃ ) ΟβΗδ H

432 H CH(CH ₃ ) N(CH ₃ ) 4-CI-C ₆ H ₄ H

433 H CH(CH ₃ ) N(CH ₃ ) SCH ₃ SCH ₃

434 H CH(CH ₃ ) N(CH ₃ ) SCH ₃ H

435 H CH(CH ₃ ) N(CH ₃ ) SCH ₃ CH ₃

436 H CH(CH ₃ ) N(CH ₃ ) SCH ₃ CH ₂ CH ₃ R D Y R ³ R ⁴

437 H CH(CH ₃ ) N(CH ₃ ) SCH ₃ CH(CH ₃ ) ₂

438 H CH(CH ₃ ) N(CH ₃ ) OCH ₂ CH ₃ OCH ₂ CH ₃

439 H CH(CH ₃ ) N(CH ₃ ) OCH ₂ CH ₃ H

440 H CH(CH ₃ ) N(CH ₃ ) OCH ₂ CH ₃ CH ₃

441 H CH(CH ₃ ) N(CH ₃ ) OCH ₂ CH ₃ CH ₂ CH ₃

442 H CH(CH ₃ ) N(CH ₃ ) OCH ₂ CH ₃ CH(CH ₃ ) ₂

443 H CH(CH ₃ ) N(CH ₃ ) -CH ₂ -CH ₂ -CH ₂ -

444 H CH(CH ₃ ) N(CH ₃ ) -CH ₂ -CH ₂ -CH ₂ -CH ₂ -

445 H CH(CH ₃ ) N(CH ₃ ) -CH ₂ -CH ₂ -CH ₂ -CH ₂ -CH ₂ -

446 H CH(CH ₃ ) N(CH ₃ ) -S-CH=CH-S-

447 H CH(CH ₃ ) N(CH ₃ ) -S-CH ₂ -CH ₂ -S-

448 H CH(CH ₃ ) N(CH ₃ ) -S-CH ₂ -CH ₂ -CH ₂ -S-

449 H CH(CH ₃ ) N(CH ₃ ) -NH-CH ₂ -CH ₂ -NH-

450 H CH(CH ₃ ) N(CH ₃ ) -N(CH ₃ )-CH ₂ -CH ₂ -N(CH ₃ )-

451 H CH(CH ₃ ) N-C(=0)-CH ₃ H H

452 H CH(CH ₃ ) N-C(=0)-CH ₃ CH ₃ H

453 H CH(CH ₃ ) N-C(=0)-CH ₃ CH ₂ CH ₃ H

454 H CH(CH ₃ ) N-C(=0)-CH ₃ CH(CH ₃ ) ₂ H

455 H CH(CH ₃ ) N-C(=0)-CH ₃ CH ₃ CH ₃

456 H CH(CH ₃ ) N-C(=0)-CH ₃ CH ₂ CH ₃ CH ₃

457 H CH(CH ₃ ) N-C(=0)-CH ₃ CH(CH ₃ ) ₂ CH ₃

458 H CH(CH ₃ ) N-C(=0)-CH ₃ CH ₂ CH ₃ CH ₂ CH ₃

459 H CH(CH ₃ ) N-C(=0)-CH ₃ CH(CH ₃ ) ₂ CH ₂ CH ₃

460 H CH(CH ₃ ) N-C(=0)-CH ₃ CH(CH ₃ ) ₂ CH(CH ₃ ) ₂

461 H CH(CH ₃ ) N-C(=0)-CH ₃ H

462 H CH(CH ₃ ) N-C(=0)-CH ₃ 4-CI-C ₆ H ₄ H

463 H CH(CH ₃ ) N-C(=0)-CH ₃ SCH ₃ SCH ₃

464 H CH(CH ₃ ) N-C(=0)-CH ₃ SCH ₃ H

465 H CH(CH ₃ ) N-C(=0)-CH ₃ SCH ₃ CH ₃

466 H CH(CH ₃ ) N-C(=0)-CH ₃ SCH ₃ CH ₂ CH ₃

467 H CH(CH ₃ ) N-C(=0)-CH ₃ SCH ₃ CH(CH ₃ ) ₂

468 H CH(CH ₃ ) N-C(=0)-CH ₃ OCH ₂ CH ₃ OCH ₂ CH ₃

469 H CH(CH ₃ ) N-C(=0)-CH ₃ OCH ₂ CH ₃ H

R D Y R ³ R ⁴

569 H CH2-CH2 N(CH ₃ ) -NH-CH2-CH2-NH-

570 H CH2-CH2 N(CH ₃ ) -N(CH ₃ )-CH ₂ -CH ₂ -N(CH ₃ )-

571 H CH2-CH2 N-C(=0)-CH ₃ H H

572 H CH2-CH2 N-C(=0)-CH ₃ CH ₃ H

573 H CH2-CH2 N-C(=0)-CH ₃ CH ₂ CH ₃ H

574 H CH2-CH2 N-C(=0)-CH ₃ CH(CH ₃ ) ₂ H

575 H CH2-CH2 N-C(=0)-CH ₃ CH ₃ CH ₃

576 H CH2-CH2 N-C(=0)-CH ₃ CH ₂ CH ₃ CH ₃

577 H CH2-CH2 N-C(=0)-CH ₃ CH(CH ₃ ) ₂ CH ₃

578 H CH2-CH2 N-C(=0)-CH ₃ CH ₂ CH ₃ CH ₂ CH ₃

579 H CH2-CH2 N-C(=0)-CH ₃ CH(CH ₃ ) ₂ CH ₂ CH ₃

580 H CH2-CH2 N-C(=0)-CH ₃ CH(CH ₃ ) ₂ CH(CH ₃ ) ₂

581 H CH2-CH2 N-C(=0)-CH ₃ C6H5 H

582 H CH2-CH2 N-C(=0)-CH ₃ 4-CI-C ₆ H ₄ H

583 H CH2-CH2 N-C(=0)-CH ₃ SCH ₃ SCH ₃

584 H CH2-CH2 N-C(=0)-CH ₃ SCH ₃ H

585 H CH2-CH2 N-C(=0)-CH ₃ SCH ₃ CH ₃

586 H CH2-CH2 N-C(=0)-CH ₃ SCH ₃ CH ₂ CH ₃

587 H CH2-CH2 N-C(=0)-CH ₃ SCH ₃ CH(CH ₃ ) ₂

588 H CH2-CH2 N-C(=0)-CH ₃ OCH ₂ CH ₃ OCH ₂ CH ₃

589 H CH2-CH2 N-C(=0)-CH ₃ OCH ₂ CH ₃ H

590 H CH2-CH2 N-C(=0)-CH ₃ OCH ₂ CH ₃ CH ₃

591 H CH2-CH2 N-C(=0)-CH ₃ OCH ₂ CH ₃ CH ₂ CH ₃

592 H CH2-CH2 N-C(=0)-CH ₃ OCH ₂ CH ₃ CH(CH ₃ ) ₂

593 H CH2-CH2 N-C(=0)-CH ₃ -CH2-CH2-CH2-

594 H CH2-CH2 N-C(=0)-CH ₃ -CH2-CH2-CH2-CH2-

595 H CH2-CH2 N-C(=0)-CH ₃ -CH2-CH2-CH2-CH2-CH2-

596 H CH2-CH2 N-C(=0)-CH ₃ -S-CH=CH-S-

597 H CH2-CH2 N-C(=0)-CH ₃ -S-CH2-CH2-S-

598 H CH2-CH2 N-C(=0)-CH ₃ -S-CH2-CH2-CH2-S-

599 H CH2-CH2 N-C(=0)-CH ₃ -NH-CH2-CH2-NH-

600 H CH2-CH2 N-C(=0)-CH ₃ -N(CH ₃ )-CH ₂ -CH ₂ -N(CH ₃ )-

601 H D1 0 H H

R D Y R ³ R ⁴

668 H D1 N(CH ₃ ) CH ₂ CH ₃ CH ₂ CH ₃

669 H D1 N(CH ₃ ) CH(CH ₃ ) ₂ CH ₂ CH ₃

670 H D1 N(CH ₃ ) CH(CH ₃ ) ₂ CH(CH ₃ ) ₂

671 H D1 N(CH ₃ ) H

672 H D1 N(CH ₃ ) 4-CI-C ₆ H ₄ H

673 H D1 N(CH ₃ ) SCH ₃ SCH ₃

674 H D1 N(CH ₃ ) SCH ₃ H

675 H D1 N(CH ₃ ) SCH ₃ CH ₃

676 H D1 N(CH ₃ ) SCH ₃ CH ₂ CH ₃

677 H D1 N(CH ₃ ) SCH ₃ CH(CH ₃ ) ₂

678 H D1 N(CH ₃ ) OCH ₂ CH ₃ OCH ₂ CH ₃

679 H D1 N(CH ₃ ) OCH ₂ CH ₃ H

680 H D1 N(CH ₃ ) OCH ₂ CH ₃ CH ₃

681 H D1 N(CH ₃ ) OCH ₂ CH ₃ CH ₂ CH ₃

682 H D1 N(CH ₃ ) OCH ₂ CH ₃ CH(CH ₃ ) ₂

683 H D1 N(CH ₃ ) -CH ₂ -CH ₂ -CH ₂ -

684 H D1 N(CH ₃ ) -CH ₂ -CH ₂ -CH ₂ -CH ₂ -

685 H D1 N(CH ₃ ) -CH ₂ -CH ₂ -CH ₂ -CH ₂ -CH ₂ -

686 H D1 N(CH ₃ ) -S-CH=CH-S-

687 H D1 N(CH ₃ ) -S-CH ₂ -CH ₂ -S-

688 H D1 N(CH ₃ ) -S-CH ₂ -CH ₂ -CH ₂ -S-

689 H D1 N(CH ₃ ) -NH-CH ₂ -CH ₂ -NH-

690 H D1 N(CH ₃ ) -N(CH ₃ )-CH ₂ -CH ₂ -N(CH ₃ )-

691 H D1 N-C(=0)-CH ₃ H H

692 H D1 N-C(=0)-CH ₃ CH ₃ H

693 H D1 N-C(=0)-CH ₃ CH ₂ CH ₃ H

694 H D1 N-C(=0)-CH ₃ CH(CH ₃ ) ₂ H

695 H D1 N-C(=0)-CH ₃ CH ₃ CH ₃

696 H D1 N-C(=0)-CH ₃ CH ₂ CH ₃ CH ₃

697 H D1 N-C(=0)-CH ₃ CH(CH ₃ ) ₂ CH ₃

698 H D1 N-C(=0)-CH ₃ CH ₂ CH ₃ CH ₂ CH ₃

699 H D1 N-C(=0)-CH ₃ CH(CH ₃ ) ₂ CH ₂ CH ₃

700 H D1 N-C(=0)-CH ₃ CH(CH ₃ ) ₂ CH(CH ₃ ) ₂ R D Y R ³ R ⁴

701 H D1 N-C(=0)-CH ₃ H

702 H D1 N-C(=0)-CH ₃ 4-CI-C ₆ H ₄ H

703 H D1 N-C(=0)-CH ₃ SCH ₃ SCH ₃

704 H D1 N-C(=0)-CH ₃ SCH ₃ H

705 H D1 N-C(=0)-CH ₃ SCH ₃ CH ₃

706 H D1 N-C(=0)-CH ₃ SCH ₃ CH ₂ CH ₃

707 H D1 N-C(=0)-CH ₃ SCH ₃ CH(CH ₃ ) ₂

708 H D1 N-C(=0)-CH ₃ OCH ₂ CH ₃ OCH ₂ CH ₃

709 H D1 N-C(=0)-CH ₃ OCH ₂ CH ₃ H

710 H D1 N-C(=0)-CH ₃ OCH ₂ CH ₃ CH ₃

71 1 H D1 N-C(=0)-CH ₃ OCH ₂ CH ₃ CH ₂ CH ₃

712 H D1 N-C(=0)-CH ₃ OCH ₂ CH ₃ CH(CH ₃ ) ₂

713 H D1 N-C(=0)-CH ₃ -CH ₂ -CH ₂ -CH ₂ -

714 H D1 N-C(=0)-CH ₃ -CH ₂ -CH ₂ -CH ₂ -CH ₂ -

715 H D1 N-C(=0)-CH ₃ -CH ₂ -CH ₂ -CH ₂ -CH ₂ -CH ₂ -

716 H D1 N-C(=0)-CH ₃ -S-CH=CH-S-

717 H D1 N-C(=0)-CH ₃ -S-CH ₂ -CH ₂ -S-

718 H D1 N-C(=0)-CH ₃ -S-CH ₂ -CH ₂ -CH ₂ -S-

719 H D1 N-C(=0)-CH ₃ -NH-CH ₂ -CH ₂ -NH-

720 H D1 N-C(=0)-CH ₃ -N(CH ₃ )-CH ₂ -CH ₂ -N(CH ₃ )-

721 H D2 0 H H

722 H D2 0 CH ₃ H

723 H D2 0 CH ₂ CH ₃ H

724 H D2 0 CH(CH ₃ ) ₂ H

725 H D2 0 CH ₃ CH ₃

726 H D2 0 CH ₂ CH ₃ CH ₃

727 H D2 0 CH(CH ₃ ) ₂ CH ₃

728 H D2 0 CH ₂ CH ₃ CH ₂ CH ₃

729 H D2 0 CH(CH ₃ ) ₂ CH ₂ CH ₃

730 H D2 0 CH(CH ₃ ) ₂ CH(CH ₃ ) ₂

731 H D2 0 H

732 H D2 0 4-CI-C ₆ H ₄ H

733 H D2 0 SCH ₃ SCH ₃

R D Y R ³ R ⁴

800 H D2 N(CH ₃ ) OCH ₂ CH ₃ CH ₃

801 H D2 N(CH ₃ ) OCH ₂ CH ₃ CH ₂ CH ₃

802 H D2 N(CH ₃ ) OCH ₂ CH ₃ CH(CH ₃ ) ₂

803 H D2 N(CH ₃ ) -CH2-CH2-CH2-

804 H D2 N(CH ₃ ) -CH2-CH2-CH2-CH2-

805 H D2 N(CH ₃ ) -CH2-CH2-CH2-CH2-CH2-

806 H D2 N(CH ₃ ) -S-CH=CH-S-

807 H D2 N(CH ₃ ) -S-CH2-CH2-S-

808 H D2 N(CH ₃ ) -S-CH2-CH2-CH2-S-

809 H D2 N(CH ₃ ) -NH-CH2-CH2-NH-

810 H D2 N(CH ₃ ) -N(CH ₃ )-CH ₂ -CH ₂ -N(CH ₃ )-

81 1 H D2 N-C(=0)-CH ₃ H H

812 H D2 N-C(=0)-CH ₃ CH ₃ H

813 H D2 N-C(=0)-CH ₃ CH ₂ CH ₃ H

814 H D2 N-C(=0)-CH ₃ CH(CH ₃ ) ₂ H

815 H D2 N-C(=0)-CH ₃ CH ₃ CH ₃

816 H D2 N-C(=0)-CH ₃ CH ₂ CH ₃ CH ₃

817 H D2 N-C(=0)-CH ₃ CH(CH ₃ ) ₂ CH ₃

818 H D2 N-C(=0)-CH ₃ CH ₂ CH ₃ CH ₂ CH ₃

819 H D2 N-C(=0)-CH ₃ CH(CH ₃ ) ₂ CH ₂ CH ₃

820 H D2 N-C(=0)-CH ₃ CH(CH ₃ ) ₂ CH(CH ₃ ) ₂

821 H D2 N-C(=0)-CH ₃ C6H5 H

822 H D2 N-C(=0)-CH ₃ 4-CI-C ₆ H ₄ H

823 H D2 N-C(=0)-CH ₃ SCH ₃ SCH ₃

824 H D2 N-C(=0)-CH ₃ SCH ₃ H

825 H D2 N-C(=0)-CH ₃ SCH ₃ CH ₃

826 H D2 N-C(=0)-CH ₃ SCH ₃ CH ₂ CH ₃

827 H D2 N-C(=0)-CH ₃ SCH ₃ CH(CH ₃ ) ₂

828 H D2 N-C(=0)-CH ₃ OCH ₂ CH ₃ OCH ₂ CH ₃

829 H D2 N-C(=0)-CH ₃ OCH ₂ CH ₃ H

830 H D2 N-C(=0)-CH ₃ OCH ₂ CH ₃ CH ₃

831 H D2 N-C(=0)-CH ₃ OCH ₂ CH ₃ CH ₂ CH ₃

832 H D2 N-C(=0)-CH ₃ OCH ₂ CH ₃ CH(CH ₃ ) ₂ R D Y R ³ R ⁴

932 H D3 N-C(=0)-CH ₃ CH ₃ H

933 H D3 N-C(=0)-CH ₃ CH ₂ CH ₃ H

934 H D3 N-C(=0)-CH ₃ CH(CH ₃ ) ₂ H

935 H D3 N-C(=0)-CH ₃ CH ₃ CH ₃

936 H D3 N-C(=0)-CH ₃ CH ₂ CH ₃ CH ₃

937 H D3 N-C(=0)-CH ₃ CH(CH ₃ ) ₂ CH ₃

938 H D3 N-C(=0)-CH ₃ CH ₂ CH ₃ CH ₂ CH ₃

939 H D3 N-C(=0)-CH ₃ CH(CH ₃ ) ₂ CH ₂ CH ₃

940 H D3 N-C(=0)-CH ₃ CH(CH ₃ ) ₂ CH(CH ₃ ) ₂

941 H D3 N-C(=0)-CH ₃ H

942 H D3 N-C(=0)-CH ₃ 4-CI-C ₆ H ₄ H

943 H D3 N-C(=0)-CH ₃ SCH ₃ SCH ₃

944 H D3 N-C(=0)-CH ₃ SCH ₃ H

945 H D3 N-C(=0)-CH ₃ SCH ₃ CH ₃

946 H D3 N-C(=0)-CH ₃ SCH ₃ CH ₂ CH ₃

947 H D3 N-C(=0)-CH ₃ SCH ₃ CH(CH ₃ ) ₂

948 H D3 N-C(=0)-CH ₃ OCH ₂ CH ₃ OCH ₂ CH ₃

949 H D3 N-C(=0)-CH ₃ OCH ₂ CH ₃ H

950 H D3 N-C(=0)-CH ₃ OCH ₂ CH ₃ CH ₃

951 H D3 N-C(=0)-CH ₃ OCH ₂ CH ₃ CH ₂ CH ₃

952 H D3 N-C(=0)-CH ₃ OCH ₂ CH ₃ CH(CH ₃ ) ₂

953 H D3 N-C(=0)-CH ₃ -CH ₂ -CH ₂ -CH ₂ -

954 H D3 N-C(=0)-CH ₃ -CH ₂ -CH ₂ -CH ₂ -CH ₂ -

955 H D3 N-C(=0)-CH ₃ -CH ₂ -CH ₂ -CH ₂ -CH ₂ -CH ₂ -

956 H D3 N-C(=0)-CH ₃ -S-CH=CH-S-

957 H D3 N-C(=0)-CH ₃ -S-CH ₂ -CH ₂ -S-

958 H D3 N-C(=0)-CH ₃ -S-CH ₂ -CH ₂ -CH ₂ -S-

959 H D3 N-C(=0)-CH ₃ -NH-CH ₂ -CH ₂ -NH-

960 H D3 N-C(=0)-CH ₃ -N(CH ₃ )-CH ₂ -CH ₂ -N(CH ₃ )-

961 H D4 0 H H

962 H D4 0 CH ₃ H

963 H D4 0 CH ₂ CH ₃ H

964 H D4 0 CH(CH ₃ ) ₂ H

R D Y R ³ R ⁴

1031 H D4 N(CH ₃ ) H

1032 H D4 N(CH ₃ ) 4-CI-C ₆ H ₄ H

1033 H D4 N(CH ₃ ) SCH ₃ SCH ₃

1034 H D4 N(CH ₃ ) SCH ₃ H

1035 H D4 N(CH ₃ ) SCH ₃ CH ₃

1036 H D4 N(CH ₃ ) SCH ₃ CH ₂ CH ₃

1037 H D4 N(CH ₃ ) SCH ₃ CH(CH ₃ ) ₂

1038 H D4 N(CH ₃ ) OCH ₂ CH ₃ OCH ₂ CH ₃

1039 H D4 N(CH ₃ ) OCH ₂ CH ₃ H

1040 H D4 N(CH ₃ ) OCH ₂ CH ₃ CH ₃

1041 H D4 N(CH ₃ ) OCH ₂ CH ₃ CH ₂ CH ₃

1042 H D4 N(CH ₃ ) OCH ₂ CH ₃ CH(CH ₃ ) ₂

1043 H D4 N(CH ₃ ) -CH ₂ -CH ₂ -CH ₂ -

1044 H D4 N(CH ₃ ) -CH ₂ -CH ₂ -CH ₂ -CH ₂ -

1045 H D4 N(CH ₃ ) -CH ₂ -CH ₂ -CH ₂ -CH ₂ -CH ₂ -

1046 H D4 N(CH ₃ ) -S-CH=CH-S-

1047 H D4 N(CH ₃ ) -S-CH ₂ -CH ₂ -S-

1048 H D4 N(CH ₃ ) -S-CH ₂ -CH ₂ -CH ₂ -S-

1049 H D4 N(CH ₃ ) -NH-CH ₂ -CH ₂ -NH-

1050 H D4 N(CH ₃ ) -N(CH ₃ )-CH ₂ -CH ₂ -N(CH ₃ )-

1051 H D4 N-C(=0)-CH ₃ H H

1052 H D4 N-C(=0)-CH ₃ CH ₃ H

1053 H D4 N-C(=0)-CH ₃ CH ₂ CH ₃ H

1054 H D4 N-C(=0)-CH ₃ CH(CH ₃ ) ₂ H

1055 H D4 N-C(=0)-CH ₃ CH ₃ CH ₃

1056 H D4 N-C(=0)-CH ₃ CH ₂ CH ₃ CH ₃

1057 H D4 N-C(=0)-CH ₃ CH(CH ₃ ) ₂ CH ₃

1058 H D4 N-C(=0)-CH ₃ CH ₂ CH ₃ CH ₂ CH ₃

1059 H D4 N-C(=0)-CH ₃ CH(CH ₃ ) ₂ CH ₂ CH ₃

1060 H D4 N-C(=0)-CH ₃ CH(CH ₃ ) ₂ CH(CH ₃ ) ₂

1061 H D4 N-C(=0)-CH ₃ H

1062 H D4 N-C(=0)-CH ₃ 4-CI-C ₆ H ₄ H

1063 H D4 N-C(=0)-CH ₃ SCH ₃ SCH ₃ R D Y R ³ R ⁴

1064 H D4 N-C(=0)-CH ₃ SCH ₃ H

1065 H D4 N-C(=0)-CH ₃ SCH ₃ CH ₃

1066 H D4 N-C(=0)-CH ₃ SCH ₃ CH ₂ CH ₃

1067 H D4 N-C(=0)-CH ₃ SCH ₃ CH(CH ₃ ) ₂

1068 H D4 N-C(=0)-CH ₃ OCH ₂ CH ₃ OCH ₂ CH ₃

1069 H D4 N-C(=0)-CH ₃ OCH ₂ CH ₃ H

1070 H D4 N-C(=0)-CH ₃ OCH ₂ CH ₃ CH ₃

1071 H D4 N-C(=0)-CH ₃ OCH ₂ CH ₃ CH ₂ CH ₃

1072 H D4 N-C(=0)-CH ₃ OCH ₂ CH ₃ CH(CH ₃ ) ₂

1073 H D4 N-C(=0)-CH ₃ -CH ₂ -CH ₂ -CH ₂ -

1074 H D4 N-C(=0)-CH ₃ -CH ₂ -CH ₂ -CH ₂ -CH ₂ -

1075 H D4 N-C(=0)-CH ₃ -CH ₂ -CH ₂ -CH ₂ -CH ₂ -CH ₂ -

1076 H D4 N-C(=0)-CH ₃ -S-CH=CH-S-

1077 H D4 N-C(=0)-CH ₃ -S-CH ₂ -CH ₂ -S-

1078 H D4 N-C(=0)-CH ₃ -S-CH ₂ -CH ₂ -CH ₂ -S-

1079 H D4 N-C(=0)-CH ₃ -NH-CH ₂ -CH ₂ -NH-

1080 H D4 N-C(=0)-CH ₃ -N(CH ₃ )-CH ₂ -CH ₂ -N(CH ₃ )-

C6H ₅ : phenyl

4-CI-C6H ₄ : 4-chlorophenyl

D1 : cyclopropan-1 ,1 -diyl

D2: cyclobutan-1 ,1 -diyl,

D3: oxiran-2 2-diyl

D4: , i.e. cyclopropan-1 ,1 -diylmethyl, where the CH ₂ moiety is attached to the nitrogen atom in formulae l-A.1 a to l-A.4d The compounds of formula (I) according to the present invention can be prepared e.g. according the preparation methods and preparation schemes as described below. Compounds of formula (I) according to the present invention can be prepared by standard methods of organic chemistry e.g. by the preparation methods and preparation schemes as described below. The definitions of Het, X, Y, W ¹ , W ² , W ³ , W ⁴ , R ¹ , R ² , R ³ , and R ⁴ of the molecular structures given in the schemes are as defined above. Room temperature means a temperature range between about 20 and 25 °C.

An examples of a general method for the preparation of compounds of formula (I) is shown below in Scheme A. Thus, construction of the heterocyclic element 3 present in compounds of formula (I) can be achieved, for example, by alkylation of the appropriate amino- heterocycle precursor 1 with the appropriate reagent of formula 2. The transformation is preferably carried out in polar solvents such as acetonitrile, acetone, 1 ,4-dioxane,

tetrahydrofuran, N,N-dimethylformamide, Ν,Ν-dimethylacetamide, N-methylpyrolidinone or a Ci- C6 alcohol or inert solvents such as: dichloromethane, 1 ,2-dichloroethane, 1 ,2- dimethoxyethane, carbon tetrachloride, tetrahydrofuran, toluene, xylenes, mesitylene, cymene, tetralone ranging between room temperature and the reflux temperature of the solvent.

Representative reaction conditions for the alkylation of compounds analogous to formula 1 are given in Tett. Lett. 201 1 , 52(23), 3033-3037. Examples of suitable leaving groups (LG) in formula 2 include, but are not limited to: halogen, alkyl sulfonate, haloalkyl sulfonate, aryl sulfonate, alkyl phosphoante. The synthesis of compounds of formula 5 can be achieved by acylation of the amine functionality in compounds of formula 3 using carboxylic acid derivatives 4 which may or may not be activated in situ. The transformation is preferably carried out in polar solvents such as acetonitrile, acetone, 1 ,4-dioxane, tetrahydrofuran, N,N-dimethylformamide, Ν,Ν-dimethylacetamide, N-methylpyrolidinone or in an inert solvent such as dichloromethane, 1 ,2-dichloroethane, or 1 ,2-dimethoxyethane at temperatures ranging between room

temperature and the reflux temperature of the solvent. A representative procedure conditions for the acylation is given in Journal of Medicinal Chemistry, 2012, 55, 7378-7391. Examples of suitable leaving groups (LG ² ) in formula 4 include, but are not limited to: halogen, alkyl sulfonate, haloalkyl sulfonate, aryl sulfonate, alkyl phosphoante, halophosphate and various activated esters derived from the reaction of a free carboxylic acid with a peptide coupling reagent in the presence of an amine base (Chem. Rev., 2011 , 111 (1 1 ), 6557-6602). A reversal of the order of these two steps would also result in an acceptable synthesis of the desired compounds. Scheme A:

In cases where Y is O or NR ⁵ compounds of formula (I) can also be prepared using an alternative strategy to install the imino functionality as is shown below in Scheme B. Thus, construction of intermediate 3 proceeds as described in Scheme A, and amine functionality present in intermediates of type 3 can then be acylated with a reagent of type 6. The transformation is preferably carried out in polar solvents such as acetonitrile, acetone, tetrahydrofuran, 1 ,4-dioxane, N,N-dimethylformamide, Ν,Ν-dimethylacetamide, N- methylpyrolidinone or a C1-C6 alcohol or in an inert solvent such as dichloromethane, 1 ,2- dichloroethane, or 1 ,2-dimethoxyethane at temperatures ranging between room temperature and the reflux temperature of the solvent. A representative procedure conditions for the acylation of is given in Journal of Chemical Ecology, 1999, 25, 7, 1543-1554. Examples of suitable leaving groups (LG ³ ) in formulae 6 include, but are not limited to: halogen, alkyl sulfonate or haloalkyi sulfonate, alkyl phosphoante, halophosphate and various activated esters derived from the reaction of the free carbonic acid with a peptide coupling reagent in the presence of an amine base (Chem. Rev., 2011 , 111 (1 1 ), 6557-6602). In the next step a compound 8 is reacted with compounds of type 7 to afford the desired structure of type 5.

Examples of suitable leaving groups (LG ⁴ ) in formulae 6 include, but are not limited to: halogen, acetate, alkyl sulfonate or haloalkyi sulfonate, alkyl phosphoante, halophosphate. The transformation is preferably carried out in polar solvents such as acetonitrile, acetone, tetrahydrofuran, 1 ,4-dioxane, N,N-dimethylformamide, Ν,Ν-dimethylacetamide, N- methylpyrolidinone, a C1-C6 alcohol or in an inert solvent such as dichloromethane, 1 ,2- dichloroethane, 1 ,2-dimethoxyethane, benzene, toluene, mesitylene, cymene, or xylenes at temperatures ranging between room temperature and the reflux temperature of the solvent, in the presence of an organic or inorganic base. Examples of suitable bases for such a transformation include but are not limited to: lithium hydroxide, sodium hydroxide, potassium hydroxide, lithium carbonate, sodium carbonate, potassium carbonate, cesium carbonate, sodium methoxide, potassium methoxide, sodium ethoxide, potassium ethoxide, lithium f- butoxide, sodium f-butoxide , potassium f-butoxide, triethylamine, diisopropyl ethyl amine, 1 ,8- diazabicyclo[5.4.0]undec-7-ene, diisopropyl amine, pyridine, sodium hydride, potassium hydride, A representative procedure conditions for such a reaction is given Journal of Medicinal Chemistry, 2000, 43, 12, 2332 - 2349. A reversal of the order of these steps would also result in an acceptable synthesis of the desired compounds of formula (I). Scheme B.

5

In cases where X is a sulfur atom, the sulfur atom is best installed in a subsequent step from the compound where X is an oxygen atom as detailed in scheme C.

Scheme C:

Here, the carbonyl compound 9 is transformed into the thiocarbonyl compound 11. The transformation is preferably carried out using a reagent of substructure 10 in polar solvents such as acetonitrile, acetone, tetrahydrofuran, Ν,Ν-dimethylformamide, or in an inert solvent such as dichloromethane, 1 ,2-dichloroethane, or 1 ,2-dimethoxyethane at temperatures ranging between room temperature and the reflux temperature of the solvent. Suitable R ^a groups in compounds of formula 10 are: Ci-C4-alkyl, aryl, such as phenyl which is unsubstituted or substituted by 1 , 2 or 3 radicals selected from halogen, Ci-C4-alkyl or Ci-C4-alkoxy. Representative reaction conditions for thionation analogous substrates are given in US 2013/102568.

The compounds of the formula (I), and their salts are in particular suitable for efficiently controlling arthropodal pests such as arachnids, myriapedes and insects as well as nematodes. The compounds of the formula (I) are especially suitable for efficiently combating insects, in particular the following pests:

Insects from the order of the lepidopterans (Lepidoptera), for example Acronicta major, Adoxophyes orana, Aedia leucomelas, Agrotis spp. such as Agrotis fucosa, Agrotis segetum, Agrotis ypsilon; Alabama argillacea, Anticarsia gemmatalis, Anticarsia spp., Argyresthia conjugella, Autographa gamma, Barathra brassicae, Bucculatrix thurberiella, Bupalus piniarius, Cacoecia murinana, Cacoecia podana, Capua reticulana, Carpocapsa pomonella, Cheimatobia brumata, Chilo spp. such as Chilo suppressalis; Choristoneura fumiferana, Choristoneura occidentalis, Cirphis unipuncta, Clysia ambiguella, Cnaphalocerus spp., Cydia pomonella, Dendrolimus pini, Diaphania nitidalis, Diatraea grandiosella, Earias insulana, Elasmopalpus lignosellus, Ephestia cautella, Ephestia kuehniella, Eupoecilia ambiguella, Euproctis

chrysorrhoea, Euxoa spp., Evetria bouliana, Feltia spp. such as Feltia subterranean; Galleria mellonella, Grapholitha funebrana, Grapholitha molesta, Helicoverpa spp. such as Helicoverpa armigera, Helicoverpa zea; Heliothis spp. such as Heliothis armigera, Heliothis virescens, Heliothis zea; Hellula undalis, Hibernia defoliaria, Hofmannophila pseudospretella, Homona magnanima, Hyphantria cunea, Hyponomeuta padella, Hyponomeuta malinellus, Keiferia lycopersicella, Lambdina fiscellaria, Laphygma spp. such as Laphygma exigua; Leucoptera coffeella, Leucoptera scitella, Lithocolletis blancardella, Lithophane antennata, Lobesia botrana, Loxagrotis albicosta, Loxostege sticticalis, Lymantria spp. such as Lymantria dispar, Lymantria monacha; Lyonetia clerkella, Malacosoma neustria, Mamestra spp. such as Mamestra brassicae; Mods repanda, Mythimna separata, Orgyia pseudotsugata, Oria spp., Ostrinia spp. such as Ostrinia nubilalis; Oulema oryzae, Panolis flammea, Pectinophora spp. such as

Pectinophora gossypiella; Peridroma saucia, Phalera bucephala, Phthorimaea spp. such as Phthorimaea operculella; Phyllocnistis citrella, Pieris spp. such as Pieris brassicae, Pieris rapae; Plathypena scabra, Plutella maculipennis, Plutella xylostella, Prodenia spp., Pseudaletia spp., Pseudoplusia includens, Pyrausta nubilalis, Rhyacionia frustrana, Scrobipalpula absoluta, Sitotroga cerealella, Sparganothis pilleriana, Spodoptera spp. such as Spodoptera frugiperda, Spodoptera littoralis, Spodoptera litura; Thaumatopoea pityocampa, Thermesia gemmatalis, Tinea pellionella, Tineola bisselliella, Tortrix viridana, Trichoplusia spp. such as Trichoplusia ni; Tuta absoluta, and Zeiraphera canadensis;

Beetles {Coleoptera), for example Acanthoscehdes obtectus, Adoretus spp., Agelastica alni, Agrilus sinuatus, Agriotes spp. such as Agriotes fuscicollis, Agriotes lineatus, Agriotes obscurus; Amphimallus solstitialis, Anisandrus dispar, Anobium punctatum, Anomala

rufocuprea, Anoplophora spp. such as Anoplophora glabripennis; Anthonomus spp. such as Anthonomus grandis, Anthonomus pomorum; Anthrenus spp., Aphthona euphoridae, Apogonia spp., Athous haemorrhoidalis, Atomaria spp. such as Atomaria linearis; Attagenus spp., Aulacophora femoralis, Blastophagus piniperda, Blitophaga undata, Bruchidius obtectus, Bruchus spp. such as Bruchus lentis, Bruchus pisorum, Bruchus rufimanus; Byctiscus betulae, Callosobruchus chinensis, Cassida nebulosa, Cerotoma trifurcata, Cetonia aurata,

Ceuthorhynchus spp. such as Ceuthorrhynchus assimilis, Ceuthorrhynchus napi; Chaetocnema tibialis, Cleonus mendicus, Conoderus spp. such as Conoderus vespertinus; Cosmopolites spp., Costelytra zealandica, Crioceris asparagi, Cryptorhynchus lapathi, Ctenicera ssp. such as Ctenicera destructor; Curculio spp., Dectes texanus, Dermestes spp., Diabrotica spp. such as Diabrotica 12-punctata Diabrotica speciosa, Diabrotica longicornis, Diabrotica semipunctata, Diabrotica virgifera; Epilachna spp. such as Epilachna varivestis, Epilachna vigintioctomaculata; Epitrix spp. such as Epitrix hirtipennis; Eutinobothrus brasiliensis, Faustinus cubae, Gibbium psylloides, Heteronychus arator, Hylamorpha elegans, Hylobius abietis, Hylotrupes bajulus, Hypera brunneipennis, Hypera postica, Hypothenemus spp., Ips typographus, Lachnosterna consanguinea, Lema bilineata, Lema melanopus, Leptinotarsa spp. such as Leptinotarsa decemlineata; Limonius califomicus, Lissorhoptrus oryzophilus, Lissorhoptrus oryzophilus, Lixus spp., Lyctus spp. such as Lyctus bruneus; Melanotus communis, Meligethes spp. such as Meligethes aeneus; Melolontha hippocastani, Melolontha melolontha, Migdolus spp.,

Monochamus spp. such as Monochamus alternatus; Naupactus xanthographus, Niptus hololeucus, Oryctes rhinoceros, Oryzaephilus surinamensis, Otiorrhynchus sulcatus,

Otiorrhynchus ovatus, Otiorrhynchus sulcatus, Oulema oryzae, Oxycetonia jucunda, Phaedon cochleariae, Phyllobius pyri, Phyllopertha horticola, Phyllophaga spp., Phyllotreta spp. such as Phyllotreta chrysocephala, Phyllotreta nemorum, Phyllotreta striolata; Phyllophaga spp., Phyllopertha horticola, Popillia japonica, Premnotrypes spp., Psylliodes chrysocephala, Ptinus spp., Rhizobius ventralis , Rhizopertha dominica, Sitona lineatus, Sitophilus spp. such as Sitophilus granaria, Sitophilus zeamais; Sphenophorus spp. such as Sphenophorus levis;

Sternechus spp. such as Sternechus subsignatus; Symphyletes spp., Tenebrio molitor, Tribolium spp. such as Tribolium castaneum; Trogoderma spp., Tychius spp., Xylotrechus spp., and Zabrus spp. such as Zabrus tenebrioides;

Flies, mosquitoes {Diptera), e.g. Aedes spp. such as Aedes aegypti, Aedes albopictus, Aedes vexans; Anastrepha ludens, Anopheles spp. such as Anopheles albimanus, Anopheles crucians, Anopheles freeborni, Anopheles gambiae, Anopheles leucosphyrus, Anopheles maculipennis, Anopheles minimus, Anopheles quadrimaculatus, Anopheles sinensis; Bibio hortulanus, Calliphora erythrocephala, Calliphora vicina, Cerafitis capitata, Ceratitis capitata, Chrysomyia spp. such as Chrysomya bezziana, Chrysomya hominivorax, Chrysomya macellaria; Chrysops atlanticus, Chrysops discalis, Chrysops silacea, Cochliomyia spp. such as Cochliomyia hominivorax; Contarinia spp. such as Contarinia sorghicola; Cordylobia anthropophaga, Culex spp. such as Culex nigripalpus, Culex pipiens, Culex quinquefasciatus, Culex tarsalis, Culex tritaeniorhynchus; Culicoides furens, Culiseta inornata, Culiseta melanura, Cuterebra spp., Dacus cucurbitae, Dacus oleae, Dasineura brassicae, Delia spp. such as Delia antique, Delia coarctata, Delia platura, Delia radicum; Dermatobia hominis, Drosophila spp., Fannia spp. such as Fannia canicularis; Gastraphilus spp. such as Gasterophilus intestinalis; Geomyza Tripunctata, Glossina fuscipes, Glossina morsitans, Glossina palpalis, Glossina tachinoides, Haematobia irritans, Haplodiplosis equestris, Hippelates spp., Hylemyia spp. such as Hylemyia platura; Hypoderma spp. such as Hypoderma lineata; Hyppobosca spp.,

Leptoconops torrens, Liriomyza spp. such as Liriomyza sativae, Liriomyza trifolii; Lucilia spp. such as Lucilia caprina, Lucilia cuprina, Lucilia sericata; Lycoria pectoralis, Mansonia titillanus, Mayetiola spp. such as Mayetiola destructor; Musca spp. such as Musca autumnalis, Musca domestica; Muscina stabulans, Oestrus spp. such as Oestrus ovis; Opomyza florum, Oscinella spp. such as Oscinella frit; Pegomya hysocyami, Phlebotomus argentipes, Phorbia spp. such as Phorbia antiqua, Phorbia brassicae, Phorbia coarctata; Prosimulium mixtum, Psila rosae, Psorophora columbiae, Psorophora discolor, Rhagoletis cerasi, Rhagoletis pomonella,

Sarcophaga spp. such as Sarcophaga haemorrhoidalis; Simulium vittatum, Stomoxys spp. such as Stomoxys calcitrans; Tabanus spp. such as Tabanus atratus, Tabanus bovinus, Tabanus lineola, Tabanus similis; Tannia spp., Tipula oleracea, Tipula paludosa, and Wohlfahrtia spp.;

Thrips {Thysanoptera). e.g. Baliothrips biformis, Dichromothrips corbetti, Dichromothrips ssp., Enneothrips flavens, Frankliniella spp. such as Frankliniella fusca, Frankliniella

occidentalis, Frankliniella tritici; Heliothrips spp., Hercinothrips femoralis, Kakothrips spp., Rhipiphorothrips cruentatus, Scirtothrips spp. such as Scirtothrips citri; Taeniothrips cardamoni, Thrips spp. such as Thrips oryzae, Thrips palmi, Thrips tabaci;

Termites (Isoptera), e.g. Calotermes flavicollis, Coptotermes formosanus, Heterotermes aureus, Heterotermes longiceps, Heterotermes tenuis, Leucotermes flavipes, Odontotermes spp., Reticulitermes spp. such as Reticulitermes speratus, Reticulitermes flavipes,

Reticulitermes grassei, Reticulitermes lucifugus, Reticulitermes santonensis, Reticulitermes virginicus; Termes natalensis;

Cockroaches (Blattaria - Blattodea), e.g. Acheta domesticus, Blatta orientalis, Blattella asahinae, Blattella germanica, Gryllotalpa spp., Leucophaea maderae, Locusta spp.,

Melanoplus spp., Periplaneta americana, Periplaneta australasiae, Periplaneta brunnea, Periplaneta fuligginosa, Periplaneta japonica;

Bugs, aphids, leafhoppers, whiteflies, scale insects, cicadas (Hemiptera), e.g.

Acrosternum spp. such as Acrosternum hilare; Acyrthosipon spp. such as Acyrthosiphon onobrychis, Acyrthosiphon pisum; Adelges laricis, Aeneolamia spp., Agonoscena spp.,

Aleurodes spp., Aleurolobus barodensis, Aleurothrixus spp., Amrasca spp., Anasa tristis, Antestiopsis spp., Anuraphis cardui, Aonidiella spp., Aphanostigma piri, Aphid ula nasturtii, Aphis spp. such as Aphis fabae, Aphis forbesi, Aphis gossypii, Aphis grossulariae, Aphis pomi, Aphis sambuci, Aphis schneideri, Aphis spiraecola; Arboridia apicalis, Arilus critatus, Aspidiella spp., Aspidiotus spp., Atanus spp., Aulacorthum solani, Bemisia spp. such as Bemisia argentifolii, Bemisia tabaci; Blissus spp. such as Blissus leucopterus; Brachycaudus cardui, Brachycaudus helichrysi, Brachycaudus persicae, Brachycaudus prunicola, Brachycolus spp., Brevicoryne brassicae, Calligypona marginata, Calocoris spp., Campylomma livida,

Capitophorus horni, Carneocephala fulgida, Cavelerius spp., Ceraplastes spp., Ceratovacuna lanigera, Cercopidae, Cerosipha gossypii, Chaetosiphon fragaefolii, Chionaspis tegalensis, Chlorita onukii, Chromaphis juglandicola, Chrysomphalus ficus, Cicadulina mbila, Cimex spp. such as Cimex hemipterus, Cimex lectularius; Coccomytilus halli, Coccus spp., Creontiades dilutus, Cryptomyzus ribis, Cryptomyzus ribis, Cyrtopeltis notatus, Dalbulus spp., Dasynus pi peris, Dialeurades spp., Diaphorina spp., Diaspis spp., Dichelops furcatus, Diconocoris hewetti, Doralis spp., Dreyfusia nordmannianae, Dreyfusia piceae, Drosicha spp., Dysaphis spp. such as Dysaphis plantaginea, Dysaphis pyri, Dysaphis radicola; Dysaulacorthum pseudosolani, Dysdercus spp. such as Dysdercus cingulatus, Dysdercus intermedius;

Dysmicoccus spp., Empoasca spp. such as Empoasca fabae, Empoasca solana; Eriosoma spp., Erythroneura spp., Eurygaster spp. such as Eurygaster integriceps; Euscelis bilobatus, Euschistus spp. such as Euschistuos heros, Euschistus impictiventris, Euschistus servus;

Geococcus coffeae, Halyomorpha spp. such as Halyomorpha halys; Heliopeltis spp.,

Homalodisca coagulata, Horcias nobilellus, Hyalopterus pruni, Hyperomyzus lactucae, lcerya spp., Idiocerus spp., Idioscopus spp., Laodelphax striatellus, Lecanium spp., Lepidosaphes spp., Leptocorisa spp., Leptoglossus phyllopus, Lipaphis erysimi, Lygus spp. such as Lygus hesperus, Lygus lineolaris, Lygus pratensis; Macropes excavatus, Macrosiphum spp. such as Macrosiphum rosae, Macrosiphum avenae, Macrosiphum euphorbiae; Mahanarva fimbriolata, Megacopta cribraria, Megoura viciae, Melanaphis pyrarius, Melanaphis sacchari, Metcafiella spp., Metopolophium dirhodum, Miridae spp., Monellia costalis, Monelliopsis pecanis, Myzus spp. such as Myzus ascalonicus, Myzus cerasi, Myzus persicae, Myzus varians; Nasonovia ribis-nigri, Nephotettix spp. such as Nephotettix malayanus, Nephotettix nigropictus, Nephotettix parvus, Nephotettix virescens; Nezara spp. such as Nezara viridula; Nilaparvata lugens, Oebalus spp., Oncometopia spp., Orthezia praelonga, Parabemisia myricae, Paratrioza spp., Parlatoria spp., Pemphigus spp. such as Pemphigus bursarius; Pentomidae, Peregrinus maidis, Perkinsiella saccharicida, Phenacoccus spp., Phloeomyzus passerinii, Phorodon humuli, Phylloxera spp., Piesma quadrata, Piezodorus spp. such as Piezodorus guildinii, Pinnaspis aspidistrae, Planococcus spp., Protopulvinaria pyriformis, Psallus seriatus, Pseudacysta persea, Pseudaulacaspis pentagona, Pseudococcus spp. such as Pseudococcus comstocki; Psylla spp. such as Psylla mall, Psylla piri; Pteromalus spp., Pyrilla spp., Quadraspidiotus spp., Quesada gigas, Rastrococcus spp., Reduvius senilis, Rhodnius spp., Rhopalomyzus ascalonicus, Rhopalosiphum spp. such as Rhopalosiphum pseudobrassicas, Rhopalosiphum insertum, Rhopalosiphum maidis, Rhopalosiphum padi; Sagatodes spp., Sahlbergella singularis, Saissetia spp., Sappaphis mala, Sappaphis mail, Scaphoides titanus, Schizaphis graminum, Schizoneura lanuginosa, Scotinophora spp., Selenaspidus articulatus, Sitobion avenae, Sogata spp., Sogatella furcifera, Solubea insularis , Stephanitis nashi, Stictocephala festina, Tenalaphara malayensis, Thyanta spp. such as Thyanta perditor; Tibraca spp.,

Tinocallis caryaefoliae, Tomaspis spp., Toxoptera spp. such as Toxoptera aurantii; Trialeurodes spp. such as Trialeurodes vaporariorum; Triatoma spp., Trioza spp., Typhlocyba spp., Unaspis spp. such as Unaspis yanonensis; and Viteus vitifolii;

Ants, bees, wasps, sawflies (Hymenoptera), e.g. Athalia rosae, Atta capiguara, Atta cephalotes, Atta cephalotes, Atta laevigata, Atta robusta, Atta sexdens, Atta texana, Bombus spp., Camponotus floridanus, Crematogaster spp., Dasymutilla occidentals, Diprion spp., Dolichovespula maculata, Hoplocampa spp. such as Hoplocampa minuta, Hoplocampa testudinea; Lasius spp. such as Lasius niger, Linepithema humile, Monomorium pharaonis, Paravespula germanica, Paravespula pennsylvanica, Paravespula vulgaris, Pheidole megacephala, Pogonomyrmex barbatus, Pogonomyrmex californicus, Polistes rubiginosa, Solenopsis geminata, Solenopsis invicta, Solenopsis richteri, Solenopsis xyloni, Vespa spp. such as Vespa crabro, and Vespula squamosal;

Crickets, grasshoppers, locusts (Orthoptera), e.g. Acheta domestica, Calliptamus italicus, Chortoicetes terminifera, Dociostaurus maroccanus, Gryllotalpa africana, Gryllotalpa gryllotalpa, Hieroglyphus daganensis, Kraussaria angulifera, Locusta migratoria, Locustana pardalina, Melanoplus bivittatus, Mela no pi us femurrubrum, Mela no pi us mexicanus, Mela no pi us sanguinipes, Melanoplus spretus, Nomadacris septemfasciata, Oedaleus senegalensis, Schistocerca americana, Schistocerca gregaria, Tachycines asynamorus, and Zonozerus variegatus;

[Earwigs {Dermaptera), e.g. forficula auricularia,

Lice {Phthiraptera), e.g. Damalinia spp., Pediculus spp. such as Pediculus humanus capitis, Pediculus humanus corporis; Pthirus pubis, Haematopinus spp. such as Haematopinus eurysternus, Haematopinus suis; Linognathus spp. such as Linognathus vituli; Bovicola bovis, Menopon gallinae, Menacanthus stramineus and Solenopotes capillatus, Trichodectes spp.; Fleas {Siphonaptera), e.g. Ceratophyllus spp., Ctenocephalides felis, Ctenocephalides cams, Xenopsylla cheopis, Pulex irritans, Tunga penetrans, and Nosopsyllus fasciatus.

The compounds of the formula (I) are also suitable for efficiently combating arthropd pests different from insects such as, in particular the following pests:

arachnids {Arachnids), such as acari,e.g. of the families Argasidae, Ixodidae and

Sarcoptidae, such as Amblyomma spp. (e.g. Amblyomma americanum, Amblyomma

variegatum, Amblyomma maculatum), Argas spp. (e.g. Argas persicus), Boophilus spp. (e.g. Boophilus annulatus, Boophilus decoloratus, Boophilus microplus), Dermacentor silvarum, Dermacentor andersoni, Dermacentor variabilis, Hyalomma spp. (e.g. Hyalomma truncatum), Ixodes spp. (e.g. Ixodes ricinus, Ixodes rubicundus, Ixodes scapularis, Ixodes holocyclus, Ixodes pacificus), Ornithodorus spp. (e.g. Ornithodorus moubata, Ornithodorus hermsi,

Ornithodorus turicata), Ornithonyssus bacoti, Otobius megnini, Dermanyssus gallinae,

Psoroptes spp. (e.g. Psoroptes ovis), Rhipicephalus spp. (e.g. Rhipicephalus sanguineus, Rhipicephalus appendiculatus, Rhipicephalus evertsi), Rhizoglyphus spp., Sarcoptes spp. (e.g. Sarcoptes scabies), and Eriophyidae spp. such as Acaria sheldoni, Aculops spp. (e.g. Aculops pelekassi) Aculus spp. (e.g. Aculus schlechtendali), Epitrimerus pyri, Phyllocoptruta oleivora and Eriophyes spp. (e.g. Eriophyes sheldoni); Tarsonemidae spp. such as Hemitarsonemus spp., Phytonemus pallidus and Polyphagotarsonemus latus, Stenotarsonemus spp.;

Tenuipalpidae spp. such as Brevipalpus spp. (e.g. Brevipalpus phoenicis); Tetranychidae spp. such as Eotetranychus spp., Eutetranychus spp., Oligonychus spp., Tetranychus cinnabarinus, Tetranychus kanzawai, Tetranychus pacificus, Tetranychus telarius and Tetranychus urticae; Bryobia praetiosa, Panonychus spp. (e.g. Panonychus ulmi, Panonychus citri), Metatetranychus spp. and Oligonychus spp. (e.g. Oligonychus pratensis), Vasates lycopersici; Araneida, e.g. Latrodectus mactans, and Loxosceles reclusa. And Acarus siro, Chorioptes spp., Scorpio maurus;

Silverfish, firebrat {Thysanura), e.g. Lepisma saccharina and Thermobia domestica;

Centipedes {Chilopoda), e.g. Geophilus spp., Scutigera spp. such as Scutigera coleoptrata;

Millipedes {Diplopoda), e.g. Blaniulus guttulatus, Narceus spp.,

Springtails (Collembola ), e.g. Onychiurus ssp. such as Onychiurus armatus,

They are also suitable for controlling nematodes: plant parasitic nematodes such as root knot nematodes, Meloidogyne hapla, Meloidogyne incognita, Meloidogyne javanica, and other Meloidogyne species; cyst-forming nematodes, Globodera rostochiensis and other Globodera species; Heterodera avenae, Heterodera glycines, Heterodera schachtii, Heterodera trifolii, and other Heterodera species; Seed gall nematodes, Anguina species; Stem and foliar nematodes, Aphelenchoides species such as Aphelenchoides besseyi ; Sting nematodes, Belonolaimus longicaudatus and other Belonolaimus species; Pine nematodes, Bursaphelenchus lignicolus Mamiya et Kiyohara, Bursaphelenchus xylophilus and other Bursaphelenchus species; Ring nematodes, Criconema species, Criconemella species, Criconemoides species,

Mesocriconema species; Stem and bulb nematodes, Ditylenchus destructor, Ditylenchus dipsaci and other Ditylenchus species; Awl nematodes, Dolichodorus species; Spiral nematodes, Heliocotylenchus multicinctus and other Helicotylenchus species; Sheath and sheathoid nematodes, Hemicycliophora species and Hemicriconemoides species;

Hirshmanniella species; Lance nematodes, Hoploaimus species; false rootknot nematodes, Nacobbus species; Needle nematodes, Longidorus elongatus and other Longidorus species; Lesion nematodes, Pratylenchus brachyurus, Pratylenchus neglectus, Pratylenchus penetrans, Pratylenchus curvitatus, Pratylenchus goodeyi and other Pratylenchus species; Burrowing nematodes, Radopholus similis and other Radopholus species; Reniform nematodes,

Rotylenchus robustus, Rotylenchus reniformis and other Rotylenchus species; Scutellonema species; Stubby root nematodes, Trichodorus primitivus and other Trichodorus species, Paratrichodorus species; Stunt nematodes, Tylenchorhynchus claytoni, Tylenchorhynchus dubius and other Tylenchorhynchus species; Citrus nematodes, Tylenchulus species such as Tylenchulus semipenetrans; Dagger nematodes, Xiphinema species; and other plant parasitic nematode species.

Examples of further pest species which may be controlled by compounds of fomula (I) include: from the class of the Bivalva, for example, Dreissena spp.; from the class of the Gastropoda, for example, Arion spp., Biomphalaria spp., Bulinus spp., Deroceras spp., Galba spp., Lymnaea spp., Oncomelania spp., Succinea spp.; from the class of the helminths, for example, Ancylostoma duodenale, Ancylostoma ceylanicum, Acylostoma braziliensis,

Ancylostoma spp., Ascaris lubricoides, Ascaris spp., Brugia malayi, Brugia timori, Bunostomum spp., Chabertia spp., Clon orchis spp., Cooperia spp., Dicrocoelium spp., Dictyocaulus filaria, Diphyllobothrium latum, Dracunculus medinensis, Echinococcus granulosus, Echinococcus multilocularis, Enterobius vermicularis, Faciola spp., Haemonchus spp. such as Haemonchus contortus; Heterakis spp., Hymenolepis nana, Hyostrongulus spp., Loa Loa, Nematodirus spp., Oesophagostomum spp., Opisthorchis spp., Onchocerca volvulus, Ostertagia spp.,

Paragonimus spp., Schistosomen spp., Strongyloides fuelleborni, Strongyloides stercora lis, Stronyloides spp., Taenia saginata, Taenia solium, Trichinella spiralis, Trichinella nativa, Trichinella britovi, Trichinella nelson i, Trichinella pseudopsiralis, Trichostrongulus spp., Trichuris trichuria, Wuchereria bancrofti; from the order of the Isopoda, for example, Armadillidium vulgare, Oniscus asellus, Porcellio scaber; from the order of the Symphyla, for example, Scutigerella immaculata.

Further examples of pest species which may be controlled by compounds of formula (I) include: Anisoplia austriaca, Apamea spp., Austroasca viridigrisea, Baliothrips biformis,

Caenorhabditis elegans, Cephus spp., Ceutorhynchus napi, Chaetocnema aridula, Chilo auricilius, Chilo indicus , Chilo polychrysus, Chortiocetes terminifera, Cnaphalocroci medinalis, Cnaphalocrosis spp., Colias eurytheme, Collops spp., Comitermes cumulans, Creontiades spp., Cyclocephala spp., Dalbulus maidis, Deraceras reticulatum , Diatrea saccharalis, Dichelops eatus, Dicladispa armigera , Diloboderus spp. such as Diloboderus abderus; Edessa spp., Epinotia spp., Formicidae, Geocoris spp., Globitermes sulfureus, Gryllotalpidae, Halotydeus destructor, Hipnodes bicolor, Hydrellia philippina, Julus spp., Laodelphax spp., Leptocorsia acuta , Leptocorsia oratorius , Liogenys fuscus, Lucillia spp., Lyogenys fuscus, Mahanarva spp., Maladera matrida, Marasmia spp., Mastotermes spp., Mealybugs, Megascelis ssp, Metamasius hemipterus, Microtheca spp., Mods latipes, Murgantia spp., Mythemina separata ,

Neocapritermes opacus, Neocapritermes parvus, Neomegalotomus spp., Neotermes spp.,

Nymphula depunctalis, Oebalus pugnax, Orseolia spp. such as Orseolia oryzae; Oxycaraenus hyalinipennis, Plusia spp., Pomacea canaliculata, Procornitermes ssp, Procornitermes triacifer , Psylloides spp., Rachiplusia spp., Rhodopholus spp., Scaptocoris casta nea, Scaptocoris spp., Scirpophaga spp. such as Scirpophaga incertulas , Scirpophaga innotata; Scotinophara spp. such as Scotinophara coarctata; Sesamia spp. such as Sesamia inferens, Sogaella frucifera, Solenapsis geminata, Spissistilus spp., Stalk borer, Stenchaetothrips biformis,

Steneotarsonemus spinki, Sylepta derogata, Telehin licus, Trichostrongylus spp..

Compounds of the formula (I) are particularly useful for controlling insects of the orders Hemiptera and Thysanoptera.

For use in a method according to the present invention, the compounds of the formula (I) can be converted into the customary formulations, e.g. solutions, emulsions, suspensions, dusts, powders, pastes, granules and directly sprayable solutions. The use form depends on the particular purpose and application method. Formulations and application methods are chosen to ensure in each case a fine and uniform distribution of the compound of the formula (I) according to the present invention.

The formulations are prepared in a known manner (see e.g. for review US 3,060,084, EP-A 707 445 (for liquid concentrates), Browning, "Agglomeration", Chemical Engineering, Dec. 4, 1967, 147-48, Perry's Chemical Engineer's Handbook, 4th Ed., McGraw-Hill, New York, 1963, pages 8-57 and et seq. WO 91/13546, US 4,172,714, US 4,144,050, US 3,920,442, US 5,180,587, US 5,232,701 , US 5,208,030, GB 2,095,558, US 3,299,566, Klingman, Weed Control as a Science, John Wiley and Sons, Inc., New York, 1961 , Hance et al., Weed Control Handbook, 8th Ed., Blackwell Scientific Publications, Oxford, 1989 and Mollet, H., Grubemann, A., Formulation technology, Wiley VCH Verlag GmbH, Weinheim (Germany), 2001 , 2. D. A. Knowles, Chemistry and Technology of Agrochemical Formulations, Kluwer Academic

Publishers, Dordrecht, 1998 (ISBN 0-7514-0443-8), for example by extending the active compound with auxiliaries suitable for the formulation of agrochemicals, such as solvents and/or carriers, if desired emulsifiers, surfactants and dispersants, preservatives, antifoaming agents, anti-freezing agents, for seed treatment formulation also optionally colorants and/or binders and/or gelling agents.

Solvents/carriers, which are suitable, are e.g.:

solvents such as water, aromatic solvents (for example Solvesso products, xylene and the like), paraffins (for example mineral fractions), alcohols (for example methanol, butanol, pentanol, benzyl alcohol), ketones (for example cyclohexanone, gamma-butyrolactone), pyrrolidones (N-metyhl-pyrrolidone (NMP),N-octylpyrrolidone NOP), acetates (glycol diacetate), alkyl lactates, lactones such as g-butyrolactone, glycols, fatty acid

dimethylamides, fatty acids and fatty acid esters, triglycerides, oils of vegetable or animal origin and modified oils such as alkylated plant oils. In principle, solvent mixtures may also be used.

carriers such as ground natural minerals and ground synthetic minerals, such as silica gels, finely divided silicic acid, silicates, talc, kaolin, attaclay, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium sulfate and magnesium sulfate, magnesium oxide, ground synthetic materials, fertilizers, such as, for example, ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas and products of vegetable origin, such as cereal meal, tree bark meal, wood meal and nutshell meal, cellulose powders and other solid carriers.

Suitable emulsifiers are nonionic and anionic emulsifiers, for example polyoxyethylene fatty alcohol ethers, alkylsulfonates and arylsulfonates.

Examples of dispersants are lignin-sulfite waste liquors and methylcellulose.

Suitable surfactants are alkali metal, alkaline earth metal and ammonium salts of lignosulfonic acid, naphthalenesulfonic acid, phenolsulfonic acid, dibutylnaphthalenesulfonic acid, alkylarylsulfonates, alkyl sulfates, alkylsulfonates, fatty alcohol sulfates, fatty acids and sulfated fatty alcohol glycol ethers, furthermore condensates of sulfonated naphthalene and naphthalene derivatives with formaldehyde, condensates of naphthalene or of

naphthalenesulfonic acid with phenol and formaldehyde, polyoxyethylene octylphenyl ether, ethoxylated isooctylphenol, octylphenol, nonylphenol, alkylphenyl polyglycol ethers, tributylphenyl polyglycol ether, tristearylphenyl polyglycol ether, alkylaryl polyether alcohols, alcohol and fatty alcohol/ethylene oxide condensates, ethoxylated castor oil, polyoxyethylene alkyl ethers, ethoxylated polyoxypropylene, lauryl alcohol polyglycol ether acetal, sorbitol esters, Also anti-freezing agents such as glycerin, ethylene glycol, propylene glycol and bactericides such as can be added to the formulation.

Suitable antifoaming agents are for example antifoaming agents based on silicon or magnesium stearate.

Suitable preservatives are for example dichlorophen und benzyl alcohol hemiformal Suitable thickeners are compounds which confer a pseudoplastic flow behavior to the formulation, i.e. high viscosity at rest and low viscosity in the agitated stage. Mention may be made, in this context, for example, of commercial thickeners based on polysaccharides, such as Xanthan Gum ^® (Kelzan ^® from Kelco), Rhodopol ^® 23 (Rhone Poulenc) or Veegum ^® (from R.T. Vanderbilt), or organic phyllosilicates, such as Attaclay ^® (from Engelhardt). Antifoam agents suitable for the dispersions according to the invention are, for example, silicone emulsions (such as, for example, Silikon ^® SRE, Wacker or Rhodorsil ^® from Rhodia), long-chain alcohols, fatty acids, organofluorine compounds and mixtures thereof. Biocides can be added to stabilize the compositions according to the invention against attack by microorganisms. Suitable biocides are, for example, based on isothiazolones such as the compounds marketed under the trademarks Proxel ^® from Avecia (or Arch) or Acticide ^® RS from Thor Chemie and Kathon ^® MK from Rohm & Haas. Suitable antifreeze agents are organic polyols, for example ethylene glycol, propylene glycol or glycerol. These are usually employed in amounts of not more than 10% by weight, based on the total weight of the active compound composition. If appropriate, the active compound compositions according to the invention may comprise 1 to 5% by weight of buffer, based on the total amount of the formulation prepared, to regulate the pH, the amount and type of the buffer used depending on the chemical properties of the active compound or the active compounds. Examples of buffers are alkali metal salts of weak inorganic or organic acids, such as, for example, phosphoric acid, boronic acid, acetic acid, propionic acid, citric acid, fumaric acid, tartaric acid, oxalic acid and succinic acid.

Substances which are suitable for the preparation of directly sprayable solutions, emulsions, pastes or oil dispersions are mineral oil fractions of medium to high boiling point, such as kerosene or diesel oil, furthermore coal tar oils and oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons, for example toluene, xylene, paraffin,

tetrahydronaphthalene, alkylated naphthalenes or their derivatives, methanol, ethanol, propanol, butanol, cyclohexanol, cyclohexanone, isophorone, strongly polar solvents, for example dimethyl sulfoxide, N-methylpyrrolidone and water. Powders, materials for spreading and dusts can be prepared by mixing or concomitantly grinding the active substances with a solid carrier.

Granules, for example coated granules, impregnated granules and homogeneous granules, can be prepared by binding the active ingredients to solid carriers. Examples of solid carriers are mineral earths such as silica gels, silicates, talc, kaolin, attaclay, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate, magnesium oxide, ground synthetic materials, fertilizers, such as, for example, ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas, and products of vegetable origin, such as cereal meal, tree bark meal, wood meal and nutshell meal, cellulose powders and other solid carriers.

In general, the formulations comprise from 0.01 to 95% by weight, preferably from 0.1 to 90% by weight, of the active ingredient. The active ingredients are employed in a purity of from 90% to 100%, preferably 95% to 100% (according to NMR spectrum).

For seed treatment purposes, respective formulations can be diluted 2-10 fold leading to concentrations in the ready to use preparations of 0,01 to 60% by weight active compound by weight, preferably 0,1 to 40% by weight.

The compound of formula (I) can be used as such, in the form of their formulations or the use forms prepared therefrom, for example in the form of directly sprayable solutions, powders, suspensions or dispersions, emulsions, oil dispersions, pastes, dustable products, materials for spreading, or granules, by means of spraying, atomizing, dusting, spreading or pouring. The use forms depend entirely on the intended purposes; they are intended to ensure in each case the finest possible distribution of the active compounds according to the invention.

The following are examples of formulations:

1 . Products for dilution with water. For seed treatment purposes, such products may be applied to the seed diluted or undiluted.

A) Water-soluble concentrates (SL, LS)

10 parts by weight of the active compound is dissolved in 90 parts by weight of water or a water-soluble solvent. As an alternative, wetters or other auxiliaries are added. The active compound dissolves upon dilution with water, whereby a formulation with 10 % (w/w) of active compound is obtained.

B) Dispersible concentrates (DC)

20 parts by weight of the active compound is dissolved in 70 parts by weight of cyclohexanone with addition of 10 parts by weight of a dispersant, for example

polyvinylpyrrolidone. Dilution with water gives a dispersion, whereby a formulation with 20% (w/w) of active compounds is obtained. C) Emulsifiable concentrates (EC)

15 parts by weight of the active compounds is dissolved in 7 parts by weight of xylene with addition of calcium dodecylbenzenesulfonate and castor oil ethoxylate (in each case 5 parts by weight). Dilution with water gives an emulsion, whereby a formulation with 15% (w/w) of active compounds is obtained.

D) Emulsions (EW, EO, ES)

25 parts by weight of the active compound is dissolved in 35 parts by weight of xylene with addition of calcium dodecylbenzenesulfonate and castor oil ethoxylate (in each case 5 parts by weight). This mixture is introduced into 30 parts by weight of water by means of an emulsifier machine (e.g. Ultraturrax) and made into a homogeneous emulsion. Dilution with water gives an emulsion, whereby a formulation with 25% (w/w) of active compound is obtained.

E) Suspensions (SC, OD, FS)

In an agitated ball mill, 20 parts by weight of the active compound is comminuted with addition of 10 parts by weight of dispersants, wetters and 70 parts by weight of water or of an organic solvent to give a fine active compound suspension. Dilution with water gives a stable suspension of the active compound, whereby a formulation with 20% (w/w) of active compound is obtained.

F) Water-dispersible granules and water-soluble granules (WG, SG)

50 parts by weight of the active compound is ground finely with addition of 50 parts by weight of dispersants and wetters and made as water-dispersible or water-soluble granules by means of technical appliances (for example extrusion, spray tower, fluidized bed). Dilution with water gives a stable dispersion or solution of the active compound, whereby a formulation with 50% (w/w) of active compound is obtained.

G) Water-dispersible powders and water-soluble powders (WP, SP, SS, WS)

75 parts by weight of the active compound are ground in a rotor-stator mill with addition of

25 parts by weight of dispersants, wetters and silica gel. Dilution with water gives a stable dispersion or solution of the active compound, whereby a formulation with 75% (w/w) of active compound is obtained.

H) Gel-Formulation (GF)

In an agitated ball mill, 20 parts by weight of the active compound is comminuted with addition of 10 parts by weight of dispersants, 1 part by weight of a gelling agent wetters and 70 parts by weight of water or of an organic solvent to give a fine active compound suspension. Dilution with water gives a stable suspension of the active compound, whereby a formulation with 20% (w/w) of active compound is obtained. 2. Products to be applied undiluted for foliar applications. For seed treatment purposes, such products may be applied to the seed diluted or undiluted.

I) Dustable powders (DP, DS)

5 parts by weight of the active compound are ground finely and mixed intimately with 95 parts by weight of finely divided kaolin. This gives a dustable product having 5% (w/w) of active compound.

J) Granules (GR, FG, GG, MG)

0.5 part by weight of the active compound is ground finely and associated with 95.5 parts by weight of carriers, whereby a formulation with 0.5% (w/w) of active compound is obtained. Current methods are extrusion, spray-drying or the fluidized bed. This gives granules to be applied undiluted for foliar use.

K) ULV solutions (UL)

10 parts by weight of the active compound is dissolved in 90 parts by weight of an organic solvent, for example xylene. This gives a product having 10% (w/w) of active compound, which is applied undiluted for foliar use.

Aqueous use forms can be prepared from emulsion concentrates, pastes or wettable powders (sprayable powders, oil dispersions) by adding water. To prepare emulsions, pastes or oil dispersions, the substances, as such or dissolved in an oil or solvent, can be homogenized in water by means of a wetter, tackifier, dispersant or emulsifier. Alternatively, it is possible to prepare concentrates composed of active substance, wetter, tackifier, dispersant or emulsifier and, if appropriate, solvent or oil, and such concentrates are suitable for dilution with water.

The active ingredient concentrations in the ready-to-use products can be varied within relatively wide ranges. In general, they are from 0.0001 to 10%, preferably from 0.01 to 1 %.

The active ingredients may also be used successfully in the ultra-low-volume process (ULV), it being possible to apply formulations comprising over 95% by weight of active ingredient, or even to apply the active ingredient without additives.

In the method of this invention compounds of formula (I) may be applied with other active ingredients, for example with other pesticides, insecticides, herbicides, fertilizers such as ammonium nitrate, urea, potash, and superphosphate, phytotoxicants and plant growth regulators, safeners and nematicides. These additional ingredients may be used sequentially or in combination with the above-described compositions, if appropriate also added only immediately prior to use (tank mix). For example, the plant(s) may be sprayed with a

composition of this invention either before or after being treated with other active ingredients.

M.1 Acetylcholine esterase (AChE) inhibitors from the class of M.1A carbamates, for example aldicarb, alanycarb, bendiocarb, benfuracarb, butocarboxim, butoxycarboxim, carbaryl, carbofuran, carbosulfan, ethiofencarb, fenobucarb, formetanate, furathiocarb, isoprocarb, methiocarb, methomyl, metolcarb, oxamyl, pirimicarb, propoxur, thiodicarb, thiofanox, trimethacarb, XMC, xylylcarb and triazamate; or from the class of

M.1 B organophosphates, for example acephate, azamethiphos, azinphos-ethyl, azinphosmethyl, cadusafos, chlorethoxyfos, chlorfenvinphos, chlormephos, chlorpyrifos, chlorpyrifos-methyl, coumaphos, cyanophos, demeton-S-methyl, diazinon, dichlorvos/ DDVP, dicrotophos, dimethoate, dimethylvinphos, disulfoton, EPN, ethion, ethoprophos, famphur, fenamiphos, fenitrothion, fenthion, fosthiazate, heptenophos, imicyafos, isofenphos, isopropyl O- (methoxyaminothio-phosphoryl) salicylate, isoxathion, malathion, mecarbam,

methamidophos, methidathion, mevinphos, monocrotophos, naled, omethoate, oxydemeton- methyl, parathion, parathion-methyl, phenthoate, phorate, phosalone, phosmet, phosphamidon, phoxim, pirimiphos- methyl, profenofos, propetamphos, prothiofos, pyraclofos, pyridaphenthion, quinalphos, sulfotep, tebupirimfos, temephos, terbufos, tetrachlorvinphos, thiometon, triazophos, trichlorfon and vamidothion;

M.2. GABA-gated chloride channel antagonists such as:

M.2A cyclodiene organochlorine compounds, as for example endosulfan or chlordane; or M.2B fiproles (phenylpyrazoles), as for example ethiprole, fipronil, flufiprole, pyrafluprole and pyriprole;

M.3 Sodium channel modulators from the class of

M.3A pyrethroids, for example acrinathrin, allethrin, d-cis-trans allethrin, d-trans allethrin, bifenthrin, bioallethrin, bioallethrin S-cylclopentenyl, bioresmethrin, cycloprothrin, cyfluthrin, beta-cyfluthrin, cyhalothrin, lambda-cyhalothrin, gamma-cyhalothrin, cypermethrin, alpha- cypermethrin, beta-cypermethrin, theta-cypermethrin, zeta-cypermethrin, cyphenothrin, deltamethrin, empenthrin, esfenvalerate, etofenprox, fenpropathrin, fenvalerate, flucythrinate, flumethrin, tau-fluvalinate, halfenprox, imiprothrin, meperfluthrin,metofluthrin, momfluorothrin, permethrin, phenothrin, prallethrin, profluthrin, pyrethrin (pyrethrum), resmethrin, silafluofen, tefluthrin, tetramethylfluthrin, tetramethrin, tralomethrin and transfluthrin; or

M.3B sodium channel modulators such as DDT or methoxychlor;

M.4 Nicotinic acetylcholine receptor agonists (nAChR) from the class of

M.4A neonicotinoids, for example acteamiprid, chlothianidin, dinotefuran, imidacloprid, nitenpyram, thiacloprid and thiamethoxam; or the compounds

M.4A.1 : 1 -[(6-chloro-3-pyridinyl)methyl]-2,3,5,6,7,8-hexahydro-9-nitr o-(5S,8R)-5,8-Epoxy- 1 H-imidazo[1 ,2-a]azepine; or M.4A.2: 1 -[(6-chloro-3-pyridyl)methyl]-2-nitro-1 -[(E)-pentylideneamino]guanidine; or M4.A.3: 1 -[(6-chloro-3-pyridyl)methyl]-7-methyl-8-nitro-5-propoxy-3,5 ,6,7-tetrahydro-2H- imidazo[1 ,2-a]pyridine;

or M.4B nicotine.

M.5 Nicotinic acetylcholine receptor allosteric activators from the class of spinosyns, for example spinosad or spinetoram;

M.6 Chloride channel activators from the class of avermectins and milbemycins, for example abamectin, emamectin benzoate, ivermectin, lepimectin or milbemectin;

M.7 Juvenile hormone mimics, such as

M.7A juvenile hormone analogues as hydroprene, kinoprene and methoprene; or others as M.7B fenoxycarb or M.7C pyriproxyfen;

M.8 miscellaneous non-specific (multi-site) inhibitors, for example

M.8A alkyl halides as methyl bromide and other alkyl halides, or

M.8B chloropicrin, or M.8C sulfuryl fluoride, or M.8D borax, or M.8E tartar emetic;

M.9 Selective homopteran feeding blockers, for example

M.9B pymetrozine, or M.9C flonicamid;

M.10 Mite growth inhibitors, for example

M.1 OA clofentezine, hexythiazox and diflovidazin, or M.1 OB etoxazole;

M.1 1 Microbial disruptors of insect midgut membranes, for example bacillus thuringiensis or bacillus sphaericus and the insecticdal proteins they produce such as bacillus thuringiensis subsp. israelensis, bacillus sphaericus, bacillus thuringiensis subsp. aizawai, bacillus thuringiensis subsp. kurstaki and bacillus thuringiensis subsp. tenebrionis, or the Bt crop proteins: CrylAb, CrylAc, Cryl Fa, Cry2Ab, mCry3A, Cry3Ab, Cry3Bb and Cry34/35Ab1 ;

M.12 Inhibitors of mitochondrial ATP synthase, for example

M.12A diafenthiuron, or

M.12B organotin miticides such as azocyclotin, cyhexatin or fenbutatin oxide, or M.12C propargite, or M.12D tetradifon;

M.13 Uncouplers of oxidative phosphorylation via disruption of the proton gradient, for example chlorfenapyr, DNOC or sulfluramid;

M.14 Nicotinic acetylcholine receptor (nAChR) channel blockers, for example nereistoxin analogues as bensultap, cartap hydrochloride, thiocyclam or thiosultap sodium;

M.15 Inhibitors of the chitin biosynthesis type 0, such as benzoylureas as for example bistrifluron, chlorfluazuron, diflubenzuron, flucycloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, teflubenzuron or triflumuron;

M.16 Inhibitors of the chitin biosynthesis type 1 , as for example buprofezin; M.17 Moulting disruptors, Dipteran, as for example cyromazine;

M.18 Ecdyson receptor agonists such as diacylhydrazines, for example methoxyfenozide, tebufenozide, halofenozide, fufenozide or chromafenozide;

M.19 Octopamin receptor agonists, as for example amitraz;

M.20 Mitochondrial complex III electron transport inhibitors, for example

M.20A hydramethylnon, or M.20B acequinocyl, or M.20C fluacrypyrim;

M.21 Mitochondrial complex I electron transport inhibitors, for example

M.21 A METI acaricides and insecticides such as fenazaquin, fenpyroximate, pyrimidifen, pyridaben, tebufenpyrad or tolfenpyrad, or M.21 B rotenone;

M.22 Voltage-dependent sodium channel blockers, for example

M.22A indoxacarb, or M.22B metaflumizone, or M.22C 1 -[(E)-[2-(4-cyanophenyl)-1 -[3- (trifluoromethyl)phenyl]ethylidene]amino]-3-[4-(difluorometh oxy)phenyl]urea;

M.23 Inhibitors of the of acetyl CoA carboxylase, such as Tetronic and Tetramic acid derivatives, for example spirodiclofen, spiromesifen or spirotetramat;

M.24 Mitochondrial complex IV electron transport inhibitors, for example

M.24A phosphine such as aluminium phosphide, calcium phosphide, phosphine or zinc phosphide, or M.24B cyanide.

M.25 Mitochondrial complex II electron transport inhibitors, such as beta-ketonitrile derivatives, for example cyenopyrafen or cyflumetofen;

M.28 Ryanodine receptor-modulators from the class of diamides, as for example flubendiamide, chlorantraniliprole (rynaxypyr®), cyantraniliprole (cyazypyr®), or the phthalamide compounds

M.28.1 : (R)-3-Chlor-N1 -{2-methyl-4-[1 ,2,2,2-tetrafluor-1 -(trifluormethyl)ethyl]phenyl}-N2- (1 -methyl-2-methylsulfonylethyl)phthalamid and

M.28.2: (S)-3-Chlor-N1 -{2-methyl-4-[1 ,2,2,2-tetrafluor-1 -(trifluormethyl)ethyl]phenyl}-N2-

(1 -methyl-2-methylsulfonylethyl)phthalamid, or the compound

M.28.3: 3-bromo-N-{2-bromo-4-chloro-6-[(1 -cyclopropylethyl)carbamoyl]phenyl}-1 -(3- chlorpyridin-2-yl)-1 H-pyrazole-5-carboxamide (proposed ISO name: cyclaniliprole), or the compound

M.28.4: methyl-2-[3,5-dibromo-2-({[3-bromo-1 -(3-chlorpyridin-2-yl)-1 H-pyrazol-5- yl]carbonyl}amino)benzoyl]-1 ,2-dimethylhydrazinecarboxylate; or a compound selected from M.28.5a) to M.28.5I):

M.28.5a) N-[4,6-dichloro-2-[(diethyl-lambda-4-sulfanylidene)carbamoyl ]-phenyl]-2-(3- chloro-2-pyridyl)-5-(trifluoromethyl)pyrazole-3-carboxamide; M.28.5b) N-[4-chloro-2-[(diethyl-lambda-4-sulfanylidene)carbamoyl]-6- methyl-phenyl]-2- (3-chloro-2-pyridyl)-5-(trifluoromethyl)pyrazole-3-carboxami de;

M.28.5c) N-[4-chloro-2-[(di-2-propyl-lambda-4-sulfanylidene)carbamoyl ]-6-methyl-phenyl]- 2-(3-chloro-2-pyridyl)-5-(trifluoromethyl)pyrazole-3-carboxa mide;

M.28.5d) N-[4,6-dichloro-2-[(di-2-propyl-lambda-4-sulfanylidene)carba moyl]-phenyl]-2-(3- chloro-2-pyridyl)-5-(trifluoromethyl)pyrazole-3-carboxamide;

M.28.5e) N-[4,6-dichloro-2-[(diethyl-lambda-4-sulfanylidene)carbamoyl ]-phenyl]-2-(3- chloro-2-pyridyl)-5-(difluoromethyl)pyrazole-3-carboxamide;

M.28.5f) N-[4,6-dibromo-2-[(di-2-propyl-lambda-4-sulfanylidene)carbam oyl]-phenyl]-2-(3- chloro-2-pyridyl)-5-(trifluoromethyl)pyrazole-3-carboxamide;

M.28.5g) N-[4-chloro-2-[(di-2-propyl-lambda-4-sulfanylidene)carbamoyl ]-6-cyano-phenyl]- 2-(3-chloro-2-pyridyl)-5-(trifluoromethyl)pyrazole-3-carboxa mide;

M.28.5h) N-[4,6-dibromo-2-[(diethyl-lambda-4-sulfanylidene)carbamoyl] -phenyl]-2-(3- chloro-2-pyridyl)-5-(trifluoromethyl)pyrazole-3-carboxamide;

Μ.28.5Ϊ) N-[2-(5-amino-1 ,3,4-thiadiazol-2-yl)-4-chloro-6-methyl-phenyl]-5-bromo-2-(3 - chloro-2-pyridyl)pyrazole-3-carboxamide;

M.28.5j) 5-chloro-2-(3-chloro-2-pyridyl)-N-[2,4-dichloro-6-[(1 -cyano-1 -methyl- ethyl)carbamoyl]phenyl]pyrazole-3-carboxamide;

M.28.5k) 5-bromo-N-[2,4-dichloro-6-(methylcarbamoyl)phenyl]-2-(3,5-di chloro-2- pyridyl)pyrazole-3-carboxamide;

M.28.5I) N-[2-(tert-butylcarbamoyl)-4-chloro-6-methyl-phenyl]-2-(3-ch loro-2-pyridyl)-5- (fluoromethoxy)pyrazole-3-carboxamide; or a compound selected from

M.28.6 N2-(1 -cyano-1 -methyl-ethyl)-N1 -(2,4-dimethylphenyl)-3-iodo-phthalamide; or

M.28.7 3-chloro-N2-(1 -cyano-1 -methyl-ethyl)-N1 -(2,4-dimethylphenyl)phthalamide;

M.UN.X insecticidal active compounds of unknown or uncertain mode of action, as for example afidopyropen, azadirachtin, amidoflumet, benzoximate, bifenazate, bromopropylate, chinomethionat, cryolite, dicofol, flufenerim, flometoquin, fluensulfone, flupyradifurone, piperonyl butoxide, pyridalyl, pyrifluquinazon, sulfoxaflor, pyflubumide or the compounds

M.UN.X.1 : 4-[5-(3,5-Dichloro-phenyl)-5-trifluoromethyl-4,5-dihydro-iso xazol-3-yl]-2-methyl- N-[(2,2,2-trifluoro-ethylcarbamoyl)-methyl]-benzamide, or the compound

M.UN.X.2: 4-[5-[3-chloro-5-(trifluoromethyl)phenyl]-5-(trifluoromethyl )-4H-isoxazol-3-yl]-N- [2-oxo-2-(2,2,2-trifluoroethylamino)ethyl]naphthalene-1 -carboxamide, or the compound

M.UN.X.3: 1 1 -(4-chloro-2,6-dimethylphenyl)-12-hydroxy-1 ,4-dioxa-9-azadispiro[4.2.4.2]- tetradec-1 1 -en-10-one, or the compound M.UN.X.4: 3-(4'-fluoro-2,4-dimethylbiphenyl-3-yl)-4-hydroxy-8-oxa-1 -azaspiro[4.5]dec-3- en-2-one, or the compound

M.UN.X.5: 1 -[2-fluoro-4-methyl-5-[(2,2,2-trifluoroethyl)sulfinyl]phenyl ]-3-(trifluoromethyl)- 1 H-1 ,2,4-triazole-5-amine, or actives on basis of bacillus firmus (Votivo, 1-1582); or

M.UN.X.6; a compound selected from the group of

M.UN.X.6a) (E/Z)-N-[1 -[(6-chloro-3-pyridyl)methyl]-2-pyridylidene]-2,2,2-trifluor o- acetamide;

M.UN.X.6b) (E/Z)-N-[1 -[(6-chloro-5-fluoro-3-pyridyl)methyl]-2-pyridylidene]-2,2,2 -trifluoro- acetamide;

M.UN.X.6c) (E/Z)-2,2,2-trifluoro-N-[1 -[(6-fluoro-3-pyridyl)methyl]-2-pyridylidene]acetamide;

M.UN.X.6d) (E/Z)-N-[1 -[(6-bromo-3-pyridyl)methyl]-2-pyridylidene]-2,2,2-trifluoro - acetamide;

M.UN.X.6e) (E/Z)-N-[1 -[1 -(6-chloro-3-pyridyl)ethyl]-2-pyridylidene]-2,2,2-trifluoro- acetamide;

M.UN.X.6†) (E/Z)-N-[1 -[(6-chloro-3-pyridyl)methyl]-2-pyridylidene]-2,2-difluoro-a cetamide;

M.UN.X.6g) (E/Z)-2-chloro-N-[1 -[(6-chloro-3-pyridyl)methyl]-2-pyridylidene]-2,2-difluoro- acetamide;

M.UN.X.6h) (E/Z)-N-[1 -[(2-chloropyrimidin-5-yl)methyl]-2-pyridylidene]-2,2,2-trif luoro- acetamide and

M.UN.X.6i) (E/Z)-N-[1 -[(6-chloro-3-pyridyl)methyl]-2-pyridylidene]-2,2,3,3,3-pent afluoro- propanamide.); or of the compounds

M.UN.X.7: 3-[3-chloro-5-(trifluoromethyl)phenyl]-4-oxo-1 -(pyrimidin-5-ylmethyl)pyrido[1 ,2- a]pyrimidin-1 -ium-2-olate; or

M.UN.X.8: 8-chloro-N-[2-chloro-5-methoxyphenyl)sulfonyl]-6-trifluorome thyl)-imidazo[1 ,2- a]pyridine-2-carboxamide; or

M.UN.X.9: 4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4H-isoxazol-3- yl]-2-methyl-N-(1 - oxothietan-3-yl)benzamide; or

M.UN.X.10: 5-[3-[2,6-dichloro-4-(3,3-dichloroallyloxy)phenoxy]propoxy]- 1 H-pyrazole. The commercially available compounds of the group M listed above may be found in The Pesticide Manual, 15th Edition, C. D. S. Tomlin, British Crop Protection Council (201 1 ) among other publications.

The quinoline derivative flometoquin is shown in WO 2006/013896. The aminofuranone compounds flupyradifurone is known from WO 2007/1 15644. The sulfoximine compound sulfoxaflor is known from WO 2007/149134. The pyrethroid momfluorothrin is known from US 6908945. The pyrazole acaricide pyflubumide is known from WO 2007/020986. The isoxazoline compounds have been described likewise M.UN.X.1 in WO 2005/085216, M.UN.X2. in WO 2009/002809 and in WO 201 1/149749 and the isoxazoline M.UN.X.9 in WO

2013/050317. The pyripyropene derivative afidopyropen has been described in WO

2006/129714. The spiroketal-substituted cyclic ketoenol derivative M.UN.X.3 is known from WO 2006/089633 and the biphenyl-substituted spirocyclic ketoenol derivative M.UN.X.4 from WO 2008/06791 1 . Finally triazoylphenylsulfide like M.UN.X.5 have been described in WO

2006/043635 and biological control agents on basis of bacillus firmus in WO 2009/124707. The neonicotionids 4A.1 is known from WO 20120/069266 and WO 201 1/06946, the M.4.A.2 from WO 2013/003977, the M4.A.3.from WO 2010/069266.

The Metaflumizone analogue M.22C is described in CN 10171577. The phthalamides

M.28.1 and M.28.2 are both known from WO 2007/101540. The anthranilamide M.28.3 has been described in WO 2005/077934. The hydrazide compound M.28.4 has been described in WO 2007/043677. The anthranilamides M.28.5a) to M.28.5h) can be prepared as described in WO 2007/006670, WO 2013/024009 and WO 2013/024010, the anthranilamide Μ.28.5Ϊ) is described in WO 201 1/085575, the M.28.5j) in WO 2008/134969, the M.28.5k) in US

201 1/046186 and the M.28.5I) in WO 2012/034403. The diamide compounds M.28.6 and M.28.7 can be found in CN 102613183.

The compounds M.UN.X.6a) to M.UN.X.6i) listed in M.UN.X.6 have been described in WO 2012/029672. The mesoionic antagonist compound M.UN.X.7 was described in

WO 2012/0921 15, the nematicide M.UN.X.8 in WO 2013/055584 and the Pyridalyl-type analogue M.UN.X.10 in WO 2010/060379.

In another embodiment of the invention, the compounds of formula (I), or their

stereoisomers, salts, tautomers and N-oxides, may also be applied with fungicides as compound II.

The following list F of active substances, in conjunction with which the compounds according to the invention can be used, is intended to illustrate the possible combinations but does not limit them:

F.I) Respiration Inhibitors

F.1-1 ) Inhibitors of complex III at Qo site:

strobilurins: azoxystrobin, coumethoxystrobin, coumoxystrobin, dimoxystrobin,

enestroburin, fluoxastrobin, kresoxim-methyl, metominostrobin, orysastrobin, picoxystrobin, pyraclostrobin, pyrametostrobin, pyraoxystrobin, pyribencarb, triclopyricarb/chlorodincarb, trifloxystrobin, 2-[2-(2,5-dimethyl-phenoxymethyl)-phenyl]-3-methoxy-acrylic acid methyl ester and 2 (2-(3-(2,6-dichlorophenyl)-1 -methyl-allylideneaminooxymethyl)-phenyl)-2-methoxyimino-N methyl-acetamide; oxazolidinediones and imidazolinones: famoxadone, fenamidone;

F.I-2) Inhibitors of complex II (e.g. carboxamides):

carboxanilides: benodanil, benzovindiflupyr, bixafen, boscalid, carboxin, fenfuram, fenhexamid, fluopyram, flutolanil, furametpyr, isopyrazam, isotianil, mepronil, oxycarboxin, penflufen, penthiopyrad, sedaxane, tecloftalam, thifluzamide, tiadinil, 2-amino-4 methyl-thiazole-

5- carboxanilide, N-(3',4',5' trifluorobiphenyl-2 yl)-3-difluoromethyl-1 -methyl-1 H-pyrazole-4 carboxamide (fluxapyroxad), N-(4'-trifluoromethylthiobiphenyl-2-yl)-3 difluoromethyl-1 -methyl-1 H pyrazole-4-carboxamide, N-(2-(1 ,3,3-trimethyl-butyl)-phenyl)-1 ,3-dimethyl-5 fluoro-1 H-pyrazole- 4 carboxamide, 3-(difluoromethyl)-1 -methyl-N-(1 ,1 ,3-trimethylindan-4-yl)pyrazole-4- carboxamide, 3-(trifluoromethyl)-1 -methyl-N-(1 , 1 ,3-trimethylindan-4-yl)pyrazole-4-carboxamide, 1 ,3-dimethyl-N-(1 ,1 ,3-trimethylindan-4-yl)pyrazole-4-carboxamide, 3-(trifluoromethyl)-1 ,5- dimethyl-N-(1 ,1 ,3-trimethylindan-4-yl)pyrazole-4-carboxamide, 3-(difluoromethyl)-1 ,5-dimethyl- N-(1 ,1 ,3-trimethylindan-4-yl)pyrazole-4-carboxamide, 1 ,3,5-trimethyl-N-(1 ,1 ,3-trimethylindan-4- yl)pyrazole-4-carboxamide, 3-(difluoromethyl)-1 -methyl-N-(1 ,1 ,3-trimethylindan-4-yl)pyrazole-4- carboxamide, 3-(trifluoromethyl)-1 -methyl-N-(1 , 1 ,3-trimethylindan-4-yl)pyrazole-4-carboxamide, 1 ,3-dimethyl-N-(1 ,1 ,3-trimethylindan-4-yl)pyrazole-4-carboxamide, 3-(trifluoromethyl)-1 ,5- dimethyl-N-(1 ,1 ,3-trimethylindan-4-yl)pyrazole-4-carboxamide, 3-(difluoromethyl)-1 ,5-dimethyl- N-(1 ,1 ,3-trimethylindan-4-yl)pyrazole-4-carboxamide, 1 ,3,5-trimethyl-N-(1 ,1 ,3-trimethylindan-4- yl)pyrazole-4-carboxamide;

F.I-3) Inhibitors of complex III at Qi site: cyazofamid, amisulbrom, [(3S,6S,7R,8R)-8-benz- yl-3-[(3-acetoxy-4-methoxy-pyridine-2-carbonyl)amino]-6-meth yl-4,9-dioxo-1 ,5-dioxonan-7-yl] 2-methylpropanoate, [(3S,6S,7R,8R)-8-benzyl-3-[[3-(acetoxymethoxy)-4-methoxy-pyr idine- 2-carbonyl]amino]-6-methyl-4,9-dioxo-1 ,5-dioxonan-7-yl] 2-methylpropanoate, [(3S,6S,7R,8R)- 8-benzyl-3-[(3-isobutoxycarbonyloxy-4-methoxy-pyridine-2-car bonyl)amino]-6-methyl-4,9-dioxo- 1 ,5-dioxonan-7-yl] 2-methylpropanoate, [(3S,6S,7R,8R)-8-benzyl-3-[[3-(1 ,3-benzodioxol-5- ylmethoxy)-4-methoxy-pyridine-2-carbonyl]amino]-6-methyl-4,9 -dioxo-1 ,5-dioxonan-7-yl] 2- methylpropanoate, 3S,6S,7R,8R)-3-[[(3-hydroxy-4-methoxy-2-pyridinyl)carbonyl]a mino]-

6- methyl-4,9-dioxo-8-(phenylmethyl)-1 ,5-dioxonan-7-yl 2-methylpropanoate;

F.I-4) Other respiration inhibitors (complex I, uncouplers) diflumetorim; (5,8-difluoro- quinazolin-4-yl)-{2-[2-fluoro-4-(4-trifluoromethylpyridin-2- yloxy)-phenyl]-ethyl}-amine;

tecnazen;ametoctradin; silthiofam; nitrophenyl derivates: binapacryl, dinobuton, dinocap, fluazinam, ferimzone, nitrthal-isopropyl,

and including organometal compounds: fentin salts, such as fentin-acetate, fentin chloride or fentin hydroxide;

F.ll) Sterol biosynthesis inhibitors (SBI fungicides) F.II-1 ) C14 demethylase inhibitors (DMI fungicides, e.g. triazoles, imidazoles) triazoles: azaconazole, bitertanol, bromuconazole, cyproconazole, difenoconazole, diniconazole, diniconazole-M, epoxiconazole, fenbuconazole, fluquinconazole, flusilazole, flutriafol, hexaconazole, imibenconazole, ipconazole, metconazole, myclobutanil,

paclobutrazole, penconazole, propiconazole, prothioconazole, simeconazole, tebuconazole, tetraconazole, triadimefon, triadimenol, triticonazole, uniconazole, 1 -[re/-(2S;3R)-3-(2-chloro- phenyl)-2-(2,4-difluorophenyl)-oxiranylmethyl]-5-thiocyanato -1 H-[1 ,2,4]triazole, 2-[re/-(2S;3R)-3- (2-chlorophenyl)-2-(2,4-difluorophenyl)-oxiranylmethyl]-2H-[ 1 ,2,4]triazole-3-thiol;

imidazoles: imazalil, pefurazoate, oxpoconazole, prochloraz, triflumizole;

pyrimidines, pyridines and piperazines: fenarimol, nuarimol, pyrifenox, triforine, 1 -[rel- (2S;3R)-3-(2-chlorophenyl)-2-(2,4-difluorophenyl)-oxiranylme thyl]-5-thiocyanato-1 H- [1 ,2,4]triazole, 2-[rel-(2S;3R)-3-(2-chlorophenyl)-2-(2,4-difluorophenyl)-oxi ranylmethyl]- 2H-[1 ,2,4]triazole-3-thiol;

F.II-2) Delta14-reductase inhitors (Amines, e.g. morpholines, piperidines)

morpholines: aldimorph, dodemorph, dodemorph-acetate, fenpropimorph, tridemorph; piperidines: fenpropidin, piperalin; spiroketalamines: spiroxamine;

F.II-3) Inhibitors of 3-keto reductase: hydroxyanilides: fenhexamid;

F.lll) Nucleic acid synthesis inhibitors

F.III-1 ) RNA, DNA synthesis

phenylamides or acyl amino acid fungicides: benalaxyl, benalaxyl-M, kiralaxyl, metalaxyl, metalaxyl-M (mefenoxam), ofurace, oxadixyl;

isoxazoles and iosothiazolones: hymexazole, octhilinone;

F.III-2) DNA topisomerase inhibitors: oxolinic acid;

F.III-3) Nucleotide metabolism (e.g. adenosin-deaminase), hydroxy (2-amino)-pyrimidines bupirimate;

F.IV) Inhibitors of cell division and or cytoskeleton

F.IV-1 ) Tubulin inhibitors: benzimidazoles and thiophanates: benomyl, carbendazim, fuberidazole, thiabendazole, thiophanate-methyl;

triazolopyrimidines: 5-chloro-7 (4-methylpiperidin-1 -yl)-6-(2,4,6-trifluorophenyl)- [1 ,2,4]triazolo[1 ,5 a]pyrimidine;

F.IV-2) Other cell division inhibitors

benzamides and phenyl acetamides: diethofencarb, ethaboxam, pencycuron, fluopicolide, zoxamide;

F.IV-3) Actin inhibitors: benzophenones: metrafenone; pyriofenone;

F.V) Inhibitors of amino acid and protein synthesis F.V-1 ) Methionine synthesis inhibitors (anilino-pyrimidines)

anilino-pyrimidines: cyprodinil, mepanipyrim, nitrapyrin, pyrimethanil;

F.V-2) Protein synthesis inhibitors (anilino-pyrimidines)

antibiotics: blasticidin-S, kasugamycin, kasugamycin hydrochloride-hydrate, mildiomycin, streptomycin, oxytetracyclin, polyoxine, validamycin A;

F.VI) Signal transduction inhibitors

F.VI-1 ) MAP / Histidine kinase inhibitors (e.g. anilino-pyrimidines)

dicarboximides: fluoroimid, iprodione, procymidone, vinclozolin;

phenylpyrroles: fenpiclonil, fludioxonil;

F.VI-2) G protein inhibitors: quinolines: quinoxyfen;

F.VI I) Lipid and membrane synthesis inhibitors

F.VI 1-1 ) Phospholipid biosynthesis inhibitors

organophosphorus compounds: edifenphos, iprobenfos, pyrazophos;

dithiolanes: isoprothiolane;

F.VII-2) Lipid peroxidation: aromatic hydrocarbons: dicloran, quintozene, tecnazene, tolclofos-methyl, biphenyl, chloroneb, etridiazole;

F.VII-3) Carboxyl acid amides (CAA fungicides)

cinnamic or mandelic acid amides: dimethomorph, flumorph, mandiproamid, pyrimorph; valinamide carbamates: benthiavalicarb, iprovalicarb, pyribencarb, valifenalate and N-(1 - (1 -(4-cyano-phenyl)ethanesulfonyl)-but-2-yl) carbamic acid-(4-fluorophenyl) ester;

F.VII-4) Compounds affecting cell membrane permeability and fatty acids:

1 -[4-[4-[5-(2,6-difluorophenyl)-4,5-dihydro-3-isoxazolyl]-2-t hiazolyl]-1 -piperidinyl]-2-[5- methyl-3-(trifluoromethyl)-1 H-pyrazol-1 -yl]ethanone, carbamates: propamocarb, propamocarb- hydrochlorid,

F.VII-5) fatty acid amide hydrolase inhibitors: 1 -[4-[4-[5-(2,6-difluorophenyl)-4,5-dihydro- 3-isoxazolyl]-2-thiazolyl]-1 -piperidinyl]-2-[5-methyl-3-(trifluoromethyl)-1 H-pyrazol-1 -yl]ethanone;

F.VI II) Inhibitors with Multi Site Action

F.VI 11-1 ) Inorganic active substances: Bordeaux mixture, copper acetate, copper hydroxide, copper oxychloride, basic copper sulfate, sulfur;

F.VIII-2) Thio- and dithiocarbamates: ferbam, mancozeb, maneb, metam,

methasulphocarb, metiram, propineb, thiram, zineb, ziram;

F.VIII-3) Organochlorine compounds (e.g. phthalimides, sulfamides, chloronitriles): anilazine, chlorothalonil, captafol, captan, folpet, dichlofluanid, dichlorophen, flusulfamide, hexachlorobenzene, pentachlorphenole and its salts, phthalide, tolylfluanid, N-(4-chloro-2-nitro- phenyl)-N-ethyl-4-methyl-benzenesulfonamide;

F.VIII-4) Guanidines and other: guanidine, dodine, dodine free base, guazatine, guazatine-acetate, iminoctadine, iminoctadine-triacetate, iminoctadine-tris(albesilate), 2,6- dimethyl-1 H,5H-[1 ,4]dithiino[2,3-c:5,6-c']dipyrrole-1 ,3,5,7(2H,6H)-tetraone;

F.VIII-5) Ahtraquinones: dithianon;

F.IX) Cell wall synthesis inhibitors

F.IX-1 ) Inhibitors of glucan synthesis: validamycin, polyoxin B;

F.IX-2) Melanin synthesis inhibitors: pyroquilon, tricyclazole, carpropamide, dicyclomet, fenoxanil;

F.X) Plant defence inducers

F.X-1 ) Salicylic acid pathway: acibenzolar-S-methyl;

F.X-2) Others: probenazole, isotianil, tiadinil, prohexadione-calcium;

phosphonates: fosetyl, fosetyl-aluminum, phosphorous acid and its salts;

F.XI) Unknown mode of action:bronopol, chinomethionat, cyflufenamid, cymoxanil, dazomet, debacarb, diclomezine, difenzoquat, difenzoquat-methylsulfate, diphenylamin, fenpyrazamine, flumetover, flusulfamide, flutianil, methasulfocarb, nitrapyrin, nitrothal-isopropyl, oxathiapiprolin, oxin-copper, proquinazid, tebufloquin, tecloftalam, triazoxide, 2-butoxy-6-iodo-3- propylchromen-4-one, N-(cyclopropylmethoxyimino-(6-difluoro-methoxy-2,3-difluoro- phenyl)- methyl)-2-phenyl acetamide, N'-(4-(4-chloro-3-trifluoromethyl-phenoxy)-2,5-dimethyl-phen yl)-N- ethyl-N methyl formamidine, N' (4-(4-fluoro-3-trifluoromethyl-phenoxy)-2,5-dimethyl-phenyl) -N- ethyl-N-methyl formamidine, N'-(2-methyl-5-trifluoromethyl-4-(3-trimethylsilanyl-propoxy )- phenyl)-N-ethyl-N-methyl formamidine, N'-(5-difluoromethyl-2 methyl-4-(3-trimethylsilanyl- propoxy)-phenyl)-N-ethyl-N-methyl formamidine, 2-{1 -[2-(5-methyl-3-trifluoromethyl-pyrazole-1 - yl)-acetyl]-piperidin-4-yl}-thiazole-4-carboxylic acid methyl-(1 ,2,3,4-tetrahydro-naphthalen-1 -yl)- amide, 2-{1 -[2-(5-methyl-3-trifluoromethyl-pyrazole-1 -yl)-acetyl]-piperidin-4-yl}-thiazole-4- carboxylic acid methyl-(R)-1 ,2,3,4-tetrahydro-naphthalen-1 -yl-amide, methoxy-acetic acid 6-tert- butyl-8-fluoro-2,3-dimethyl-quinolin-4-yl ester and N-Methyl-2-{1 -[(5-methyl-3-trifluoromethyl-1 H- pyrazol-1 -yl)-acetyl]-piperidin-4-yl}-N-[(1 R)-1 ,2,3,4-tetrahydronaphthalen-1 -yl]-4- thiazolecarboxamide, 3-[5-(4-chloro-phenyl)-2,3-dimethyl-isoxazolidin-3 yl]-pyridine,

pyrisoxazole, 5-amino-2-isopropyl-3-oxo-4-ortho-tolyl-2,3-dihydro-pyrazole -1 carbothioic acid S- allyl ester, N-(6-methoxy-pyridin-3-yl) cyclopropanecarboxylic acid amide, 5-chloro-1 (4,6- dimethoxy-pyrimidin-2-yl)-2-methyl-1 H-benzoimidazole, 2-(4-chloro-phenyl)-N-[4-(3,4- dimethoxy-phenyl)-isoxazol-5-yl]-2-prop-2-ynyloxyacetamide; F.XI) Growth regulators: abscisic acid, amidochlor, ancymidol, 6-benzylaminopurine, brassinolide, butralin, chlormequat (chlormequat chloride), choline chloride, cyclanilide, daminozide, dikegulac, dimethipin, 2,6-dimethylpuridine, ethephon, flumetralin, flurprimidol, fluthiacet, forchlorfenuron, gibberellic acid, inabenfide, indole-3-acetic acid, maleic hydrazide, mefluidide, mepiquat (mepiquat chloride), naphthaleneacetic acid, N 6-benzyladenine, paclobutrazol, prohexadione (prohexadione-calcium), prohydrojasmon, thidiazuron,

triapenthenol, tributyl phosphorotrithioate, 2,3,5 tri iodobenzoic acid, trinexapac-ethyl and uniconazole;

F.XI I) Biological control agents

Ampelomyces quisqualis (e.g. AQ 10 ^® from Intrachem Bio GmbH & Co. KG, Germany),

Aspergillus flavus (e.g. AFLAGUARD ^® from Syngenta, CH), Aureobasidium pullulans (e.g.

BOTECTOR ^® from bio-ferm GmbH, Germany), Bacillus pumilus (e.g. NRRL Accession No. B-30087 in SONATA ^® and BALLAD ^® Plus from AgraQuest Inc., USA), Bacillus subtilis (e.g. isolate NRRL-Nr. B-21661 in RHAPSODY ^® , SERENADE ^® MAX and SERENADE ^® ASO from AgraQuest Inc., USA), Bacillus subtilis var. amyloliquefaciens FZB24 (e.g. TAEGRO ^® from Novozyme Biologicals, Inc., USA), Candida oleophila I-82 (e.g. ASPIRE ^® from Ecogen Inc., USA), Candida saitoana (e.g. BIOCURE ^® (in mixture with lysozyme) and BIOCOAT ^® from Micro Flo Company, USA (BASF SE) and Arysta), Chitosan (e.g. ARMOUR-ZEN from BotriZen Ltd., NZ), Clonostachys rosea f. catenulata, also named Gliocladium catenulatum (e.g. isolate J 1446: PRESTOP ^® from Verdera, Finland), Coniothyrium minitans (e.g. CONTANS ^® from Prophyta, Germany), Cryphonectria parasitica (e.g. Endothia parasitica from CNICM, France),

Cryptococcus albidus (e.g. YIELD PLUS ^® from Anchor Bio-Technologies, South Africa), Fusarium oxysporum (e.g. BIOFOX ^® from S.I.A.P.A., Italy, FUSACLEAN ^® from Natural Plant Protection, France), Metschnikowia fructicola (e.g. SHEMER ^® from Agrogreen, Israel),

Microdochium dimerum (e.g. ANTIBOT ^® from Agrauxine, France), Phlebiopsis gigantea (e.g. ROTSOP ^® from Verdera, Finland), Pseudozyma flocculosa (e.g. SPORODEX ^® from Plant Products Co. Ltd., Canada), Pythium oligandrum DV74 (e.g. POLYVERSUM ^® from Remeslo SSRO, Biopreparaty, Czech Rep.), Reynoutria sachlinensis (e.g. REGALIA ^® from Marrone Biolnnovations, USA), Talaromyces flavus V1 17b (e.g. PROTUS ^® from Prophyta, Germany), Trichoderma asperellum SKT-1 (e.g. ECO-HOPE ^® from Kumiai Chemical Industry Co., Ltd.,

Japan), T. atroviride LC52 (e.g. SENTINEL ^® from Agrimm Technologies Ltd, NZ), T. harzianum T-22 (e.g. PLANTSHIELD ^® der Firma BioWorks Inc., USA), T. harzianum JH 35 (e.g. ROOT PRO ^® from Mycontrol Ltd., Israel), T. harzianum T-39 (e.g. TRICHODEX ^® and TRICHODERMA 2000 ^® from Mycontrol Ltd., Israel and Makhteshim Ltd., Israel), T. harzianum and T. viride (e.g. TRICHOPEL from Agrimm Technologies Ltd, NZ), T. harzianum ICC012 and T. viride ICC080 (e.g. REMEDIER ^® WP from Isagro Ricerca, Italy), T. polysporum and T. harzianum (e.g.

BINAB ^® from BINAB Bio-Innovation AB, Sweden), T. stromaticum (e.g. TRICOVAB ^® from

C.E.P.L.A.C., Brazil), T. virens GL-21 (e.g. SOILGARD ^® from Certis LLC, USA), T. viride (e.g.

TRIECO ^® from Ecosense Labs. (India) Pvt. Ltd., Indien, BIO-CURE ^® F from T. Stanes & Co. Ltd., Indien), T. viride TV1 (e.g. T. viride TV1 from Agribiotec srl, Italy), Ulocladium oudemansii

HRU3 (e.g. BOTRY-ZEN ^® from Botry-Zen Ltd, NZ).

The commercially available compounds II of the group F listed above may be found in The

Pesticide Manual, 15th Edition, C. D. S. Tomlin, British Crop Protection Council (201 1 ) among other publications. Their preparation and their activity against harmful fungi is known (cf.:

http://www.alanwood.net/pesticides/); these substances are commercially available. The compounds described by lUPAC nomenclature, their preparation and their fungicidal activity are also known (cf. Can. J. Plant Sci. 48(6), 587-94, 1968; EP A 141 317; EP-A 152 031 ;

EP A 226 917; EP A 243 970; EP A 256 503; EP-A 428 941 ; EP-A 532 022; EP-A 1 028 125;

EP-A 1 035 122; EP A 1 201 648; EP A 1 122 244, JP 2002316902; DE 19650197;

DE 10021412; DE 102005009458; US 3,296,272; US 3,325,503; WO 98/46608; WO 99/14187;

WO 99/24413; WO 99/27783; WO 00/29404; WO 00/46148; WO 00/65913; WO 01/54501 ;

WO 01/56358; WO 02/22583; WO 02/40431 ; WO 03/10149; WO 03/1 1853; WO 03/14103;

WO 03/16286; WO 03/53145; WO 03/61388; WO 03/66609; WO 03/74491 ; WO 04/49804;

WO 04/83193; WO 05/120234; WO 05/123689; WO 05/123690; WO 05/63721 ; WO 05/87772; WO 05/87773; WO 06/15866; WO 06/87325; WO 06/87343; WO 07/82098; WO 07/90624,

WO 1 1/028657).

The invertebrate pest, e.g. the insects, arachnids and nematodes, the plant, soil or water in which the plant is growing can be contacted with the present compounds of formula (I), including their stereoisomers and tautomers, as well the salts thereof, or composition(s) containing them by any application method known in the art. As such, "contacting" includes both direct contact (applying the compounds/compositions directly on the animal pest or plant - typically to the foliage, stem or roots of the plant) and indirect contact (applying the

compounds/compositions to the locus of the animal pest or plant).

The compounds of formula (I), including their stereoisomers and tautomers, as well the salts thereof, or the pesticidal compositions comprising them may be used to protect growing plants and crops from attack or infestation by animal pests, especially insects, acaridae or arachnids by contacting the plant/crop with a pesticidally effective amount of compounds of formula (I). The term "crop" refers both to growing and harvested crops.

The compounds of the present invention and the compositions comprising them are particularly important in the control of a multitude of insects on various cultivated plants, such as cereal, root crops, oil crops, vegetables, spices, ornamentals, for example seed of durum and other wheat, barley, oats, rye, maize (fodder maize and sugar maize / sweet and field corn), soybeans, oil crops, crucifers, cotton, sunflowers, bananas, rice, oilseed rape, turnip rape, sugarbeet, fodder beet, eggplants, potatoes, grass, lawn, turf, fodder grass, tomatoes, leeks, pumpkin/squash, cabbage, iceberg lettuce, pepper, cucumbers, melons, Brassica species, melons, beans, peas, garlic, onions, carrots, tuberous plants such as potatoes, sugar cane, tobacco, grapes, petunias, geranium/pelargoniums, pansies and impatiens.

The compounds of the present invention are employed as such or in form of compositions by treating the insects or the plants, plant propagation materials, such as seeds, soil, surfaces, materials or rooms to be protected from insecticidal attack with a insecticidally effective amount of the active compounds. The application can be carried out both before and after the infection of the plants, plant propagation materials, such as seeds, soil, surfaces, materials or rooms by the insects.

The present invention also includes a method of combating animal pests which comprises contacting the animal pests, their habit, breeding ground, food supply, cultivated plants, seed, soil, area, material or environment in which the animal pests are growing or may grow, or the materials, plants, seeds, soils, surfaces or spaces to be protected from animal attack or infestation with a pesticidally effective amount of at least one active compound of the formula (I), a stereoisomers, a tautomere or a salt thereof.

Moreover, animal pests may be controlled by contacting the target pest, its food supply, habitat, breeding ground or its locus with a pesticidally effective amount of compounds of formula (I), a stereoisomer, a tautomere or a salt thereof. As such, the application may be carried out before or after the infection of the locus, growing crops, or harvested crops by the pest.

The compounds of the invention can also be applied preventively to places at which occurrence of the pests is expected.

The compounds of formula (I), including their stereoisomers and their tautomers, as well as their salts may be also used to protect growing plants from attack or infestation by pests. The use includes contacting the plant with a pesticidally effective amount of compounds of formula (I), a stereoisomer, a tautomere or a salt thereof. As such, "contacting" includes both direct contact, i.e. applying the compounds/compositions directly on the pest and/or plant - typically to the foliage, stem or roots of the plant, and indirect contact, i.e. applying the

compounds/compositions to the locus of the pest and/or plant.

"Locus" means a habitat, breeding ground, plant, seed, soil, area, material or environment in which a pest or parasite is growing or may grow. The term "plant propagation material" is to be understood to denote all the generative parts of the plant such as seeds and vegetative plant material such as cuttings and tubers (e. g. potatoes), which can be used for the multiplication of the plant. This includes seeds, roots, fruits, tubers, bulbs, rhizomes, shoots, sprouts and other parts of plants. Seedlings and young plants, which are to be transplanted after germination or after emergence from soil, may also be included. These plant propagation materials may be treated prophylactically with a plant protection compound either at or before planting or transplanting.

The term "cultivated plants" is to be understood as including plants which have been modified by breeding, mutagenesis or genetic engineering. Genetically modified plants are plants, which genetic material has been so modified by the use of recombinant DNA techniques that under natural circumstances cannot readily be obtained by cross breeding, mutations or natural recombination. Typically, one or more genes have been integrated into the genetic material of a genetically modified plant in order to improve certain properties of the plant. Such genetic modifications also include but are not limited to targeted post-transtional modification of protein(s) (oligo- or polypeptides) poly for example by glycosylation or polymer additions such as prenylated, acetylated or farnesylated moieties or PEG moieties(e.g. as disclosed in

Biotechnol Prog. 2001 Jul-Aug;17(4):720-8., Protein Eng Des Sel. 2004 Jan;17(1 ):57-66, Nat Protoc. 2007;2(5):1225-35., Curr Opin Chem Biol. 2006 Oct;10(5):487-91 . Epub 2006 Aug 28., Biomaterials. 2001 Mar;22(5):405-17, Bioconjug Chem. 2005 Jan-Feb;16(1 ):1 13-21 ).

The term "cultivated plants" is to be understood also including plants that have been rendered tolerant to applications of specific classes of herbicides, such as

hydroxy-phenylpyruvate dioxygenase (HPPD) inhibitors; acetolactate synthase (ALS) inhibitors, such as sulfonyl ureas (see e. g. US 6,222,100, WO 01/82685, WO 00/26390, WO 97/41218, WO 98/02526, WO 98/02527, WO 04/106529, WO 05/20673, WO 03/14357, WO 03/13225, WO 03/14356, WO 04/16073) or imidazolinones (see e. g. US 6,222,100, WO 01/82685, WO 00/26390, WO 97/41218, WO 98/02526, WO 98/02527, WO 04/106529, WO 05/20673, WO 03/14357, WO 03/13225, WO 03/14356, WO 04/16073); enolpyruvylshikimate-3-phosphate synthase (EPSPS) inhibitors, such as glyphosate (see e. g. WO 92/00377); glutamine synthetase (GS) inhibitors, such as glufosinate (see e. g. EP-A-0242236, EP-A-242246) or oxynil herbicides (see e. g. US 5,559,024) as a result of conventional methods of breeding or genetic engineering. Several cultivated plants have been rendered tolerant to herbicides by conventional methods of breeding (mutagenesis), for example Clearfield® summer rape (Canola) being tolerant to imidazolinones, e. g. imazamox. Genetic engineering methods have been used to render cultivated plants, such as soybean, cotton, corn, beets and rape, tolerant to herbicides, such as glyphosate and glufosinate, some of which are commercially available under the trade names RoundupReady® (glyphosate) and LibertyLink® (glufosinate).

The term "cultivated plants" is to be understood also including plants that are by the use of recombinant DNA techniques capable to synthesize one or more insecticidal proteins, especially those known from the bacterial genus Bacillus, particularly from Bacillus

thuringiensis, such as a-endotoxins, e. g. CrylA(b), CrylA(c), CrylF, CrylF(a2), CryllA(b), CrylllA, CrylllB(bl ) or Cry9c; vegetative insecticidal proteins (VIP), e. g. VIP1 , VIP2, VIP3 or VIP3A; insecticidal proteins of bacteria colonizing nematodes, for example Photorhabdus spp. or Xenorhabdus spp.; toxins produced by animals, such as scorpion toxins, arachnid toxins, wasp toxins, or other insect-specific neurotoxins; toxins produced by fungi, such

Streptomycetes toxins, plant lectins, such as pea or barley lectins; agglutinins; proteinase inhibitors, such as trypsin inhibitors, serine protease inhibitors, patatin, cystatin or papain inhibitors; ribosome-inactivating proteins (RIP), such as ricin, maize-RIP, abrin, luffin, saporin or bryodin; steroid metabolism enzymes, such as 3-hydroxysteroid oxidase, ecdysteroid-IDP- glycosyl-transferase, cholesterol oxidases, ecdysone inhibitors or HMG-CoA-reductase; ion channel blockers, such as blockers of sodium or calcium channels; juvenile hormone esterase; diuretic hormone receptors (helicokinin receptors); stilben synthase, bibenzyl synthase, chitinases or glucanases. In the context of the present invention these insecticidal proteins or toxins are to be understood expressly also as pre-toxins, hybrid proteins, truncated or otherwise modified proteins. Hybrid proteins are characterized by a new combination of protein domains, (see, for example WO 02/015701 ). Further examples of such toxins or genetically-modified plants capable of synthesizing such toxins are dis-closed, for example, in EP-A 374 753, WO 93/007278, WO 95/34656, EP-A 427 529, EP-A 451 878, WO 03/018810 und WO 03/052073. The methods for producing such genetically modified plants are generally known to the person skilled in the art and are described, for example, in the publications mentioned above. These insecticidal proteins contained in the genetically modified plants impart to the plants producing these proteins protection from harmful pests from certain taxonomic groups of arthropods, particularly to beetles (Coleoptera), flies (Diptera), and butterflies and moths (Lepidoptera) and to plant parasitic nematodes (Nematoda).

The term "cultivated plants" is to be understood also including plants that are, e.g. by the use of recombinant DNA techniques, capable of synthesizing one or more proteins in order to increase the resistance or tolerance of those plants to bacterial, viral or fungal pathogens.

Examples of such proteins are the so-called "pathogenesis-related proteins", also termed PR proteins - see, for example EP-A 0 392 225 -, or plant disease resistance genes - for example potato cultivars, which express resistance genes acting against Phytophthora infestans derived from the mexican wild potato Solarium bulbocastanum - or T4-lysozym - e. g. potato cultivars capable of synthesizing these proteins with increased resistance against bacteria such as Erwinia amylvora. The methods for producing such genetically modified plants are generally known to the person skilled in the art and are described, for example, in the publications mentioned above.

The term "cultivated plants" is to be understood also including plants that are, e.g. by the use of recombinant DNA techniques, capable of synthesizing one or more proteins to increase the productivity, e. g. bio mass production, grain yield, starch content, oil content or protein content, or to improve tolerance to drought, salinity or other growth-limiting environmental factors or tolerance to pests and fungal, bacterial or viral pathogens of those plants.

The term "cultivated plants" is to be understood also including plants that contain by the use of recombinant DNA techniques a modified amount of substances of content or new substances of content, specifically to improve human or animal nutrition, for ex-ample oil crops that produce health-promoting long-chain omega-3 fatty acids or unsaturated omega-9 fatty acids (e. g. Nexera® rape).

The term "cultivated plants" is to be understood also including plants that contain by the use of recombinant DNA techniques a modified amount of substances of content or new substances of content, specifically to improve raw material production, for example potatoes that produce increased amounts of amylopectin (e. g. Amflora® potato).

In general, "pesticidally effective amount" means the amount of active ingredient needed to achieve an observable effect on growth, including the effects of necrosis, death, retardation, prevention, and removal, destruction, or otherwise diminishing the occurrence and activity of the target organism. The pesticidally effective amount can vary for the various

compounds/compositions used in the invention. A pesticidally effective amount of the compositions will also vary according to the prevailing conditions such as desired pesticidal effect and duration, weather, target species, locus, mode of application, and the like.

In the case of soil treatment or of application to the pests dwelling place or nest, the quantity of active ingredient ranges from 0.0001 to 500 g per 100 m ² , preferably from 0.001 to 20 g per 100 m ² .

Customary application rates in the protection of materials are, for example, from 0.01 g to

1000 g of active compound per m ² treated material, desirably from 0.1 g to 50 g per m ² .

Insecticidal compositions for use in the impregnation of materials typically contain from 0.001 to 95 weight %, preferably from 0.1 to 45 weight %, and more preferably from 1 to 25 weight % of at least one repellent and/or insecticide. For use in treating crop plants, the rate of application of the active ingredients of this invention may be in the range of 0.1 g to 4000 g per hectare, desirably from 25 g to 600 g per hectare, more desirably from 50 g to 500 g per hectare.

The compounds of formula (I), including the tautomers and stereoisomers, as well as their salts, are effective through both contact, e.g. via soil, glass, wall, bed net, carpet, plant parts or animal parts, and ingestion, e.g. via ingestion of bait or plant part.

The compounds of the invention may also be applied against non-crop insect pests, such as ants, termites, wasps, flies, mosquitos, crickets, or cockroaches. For use against said non- crop pests, compounds of formula (I), including the tautomers and stereoisomers, as well as their salts, are preferably used in a bait composition.

The bait can be a liquid, a solid or a semisolid preparation (e.g. a gel). Solid baits can be formed into various shapes and forms suitable to the respective application e.g. granules, blocks, sticks, disks. Liquid baits can be filled into various devices to ensure proper application, e.g. open containers, spray devices, droplet sources, or evaporation sources. Gels can be based on aqueous or oily matrices and can be formulated to particular necessities in terms of stickyness, moisture retention or aging characteristics.

The bait employed in the composition is a product, which is sufficiently attractive to incite insects such as ants, termites, wasps, flies, mosquitos, crickets etc. or cockroaches to eat it. The attractiveness can be manipulated by using feeding stimulants or sex pheromones. Food stimulants are chosen, for example, but not exclusively, from animal and/or plant proteins (meat-, fish- or blood meal, insect parts, egg yolk), from fats and oils of animal and/or plant origin, or mono-, oligo- or polyorganosaccharides, especially from sucrose, lactose, fructose, dextrose, glucose, starch, pectin or even molasses or honey. Fresh or decaying parts of fruits, crops, plants, animals, insects or specific parts thereof can also serve as a feeding stimulant. Sex pheromones are known to be more insect specific. Specific pheromones are described in the literature and are known to those skilled in the art.

For use in bait compositions, the typical content of active ingredient is from 0.001 weight % to 15 weight %, desirably from 0.001 weight % to 5% weight % of active compound.

Formulations of compounds of formula (I), including the tautomers and stereoisomers, as well as their salts, as aerosols, e.g in spray cans, oil sprays or pump sprays are highly suitable for the non-professional user for controlling pests such as flies, fleas, ticks, mosquitos or cockroaches. Aerosol recipes are preferably composed of the active compound, solvents such as lower alcohols, e.g. methanol, ethanol, propanol or butanol, ketones, e.g. acetone, methyl ethyl ketone, paraffin hydrocarbons, e.g. kerosenes or mineral oils, having boiling ranges of approximately 50 to 250°C, dimethylformamide, N-methylpyrrolidone, dimethyl sulfoxide, aromatic hydrocarbons such as toluene, xylene, water, furthermore auxiliaries such as emulsifiers such as sorbitol monooleate, oleyl ethoxylate having 3-7 mol of ethylene oxide, fatty alcohol ethoxylate, perfume oils such as ethereal oils, esters of medium fatty acids with lower alcohols, aromatic carbonyl compounds, if appropriate stabilizers such as sodium benzoate, amphoteric surfactants, lower epoxides, triethyl orthoformate and, if required, propellants such as propane, butane, nitrogen, compressed air, dimethyl ether, carbon dioxide, nitrous oxide, or mixtures of these gases.

The oil spray formulations differ from the aerosol recipes in that no propellants are used. For use in spray compositions, the content of active ingredient is from 0.001 to 80 weights %, preferably from 0.01 to 50 weight % and most preferably from 0.01 to 15 weight %.

The compounds of formula (I), including the tautomers and stereoisomers, as well as their salts, and their respective compositions can also be used in mosquito and fumigating coils, smoke cartridges, vaporizer plates or long-term vaporizers and also in moth papers, moth pads or other heat-independent vaporizer systems.

Methods to control infectious diseases transmitted by insects, such as malaria, dengue and yellow fever, lymphatic filariasis, and leishmaniasis, with compounds of formula (I) or the stereoisomers, tautomers or salts thereof, and with their respective compositions also comprise treating surfaces of huts and houses, air spraying and impregnation of curtains, tents, clothing items, bed nets, tsetse-fly trap or the like. Insecticidal compositions for application to fibers, fabric, knitgoods, nonwovens, netting material or foils and tarpaulins preferably comprise a mixture including the insecticide, optionally a repellent and at least one binder. Suitable repellents for example are Ν,Ν-Diethyl-meta-toluamide (DEET), N,N-diethylphenylacetamide (DEPA), 1 -(3-cyclohexan-1 -yl-carbonyl)-2-methylpiperine, (2-hydroxymethylcyclohexyl) acetic acid lactone, 2-ethyl-1 ,3-hexandiol, indalone, Methylneodecanamide (MNDA), a pyrethroid not used for insect control such as {(+/-)-3-allyl-2-methyl-4-oxocyclopent-2-(+)-enyl-(+)-trans- chrysantemate (Esbiothrin), a repellent derived from or identical with plant extracts like limonene, eugenol, (+)-Eucamalol (1 ), (-)-l -epi-eucamalol or crude plant extracts from plants like Eucalyptus maculata, Vitex rotundifolia, Cymbopogan martinii, Cymbopogan citratus (lemon grass), Cymopogan nartdus (citronella). Suitable binders are selected for example from polymers and copolymers of vinyl esters of aliphatic acids (such as such as vinyl acetate and vinyl versatate), acrylic and methacrylic esters of alcohols, such as butyl acrylate, 2- ethylhexylacrylate, and methyl acrylate, mono- and di-ethylenically unsaturated hydrocarbons, such as styrene, and aliphatic diens, such as butadiene.

The impregnation of curtains and bednets is done in general by dipping the textile material into emulsions or dispersions of the insecticide or spraying them onto the nets. The compounds of formula (I), including the tautomers and stereoisomers, as well as their salts, and their compositions can be used for protecting wooden materials such as trees, board fences, sleepers, etc. and buildings such as houses, outhouses, factories, but also construction materials, furniture, leathers, fibers, vinyl articles, electric wires and cables etc. from ants and/or termites, and for controlling ants and termites from doing harm to crops or human being, e.g. when the pests invade into houses and public facilities. The compounds of formula (I), their stereoisomers, their tautomers or their salts are applied not only to the surrounding soil surface or into the under-floor soil in order to protect wooden materials but it can also be applied to lumbered articles such as surfaces of the under-floor concrete, alcove posts, beams, plywoods, furniture, etc., wooden articles such as particle boards, half boards, etc. and vinyl articles such as coated electric wires, vinyl sheets, heat insulating material such as styrene foams, etc. In case of application against ants doing harm to crops or human beings, the ant controller of the present invention is applied to the crops or the surrounding soil, or is directly applied to the nest of ants or the like.

The compounds of formula (I), including the tautomers and stereoisomers, as well as their salts, are also suitable for the treatment of seeds in order to protect the seed from insect pest, in particular from soil-living insect pests and the resulting plant's roots and shoots against soil pests and foliar insects.

The compounds of formula (I), including the tautomers and stereoisomers, as well as their salts, are particularly useful for the protection of the seed from soil pests and the resulting plant's roots and shoots against soil pests and foliar insects. The protection of the resulting plant's roots and shoots is preferred. More preferred is the protection of resulting plant's shoots from piercing and sucking insects, wherein the protection from aphids is most preferred.

The present invention therefore comprises a method for the protection of seeds from insects, in particular from soil insects and of the seedling's roots and shoots from insects, in particular from soil and foliar insects, said method comprising contacting the seeds before sowing and/or after pregermination with a compound of the general formula (I), a tautomer, a stereosiomer or a salt thereof. Particularly preferred is a method, wherein the plant's roots and shoots are protected, more preferably a method, wherein the plants shoots are protected form piercing and sucking insects, most preferably a method, wherein the plants shoots are protected from aphids.

The term seed includes seeds and plant propagules of all kinds including but not limited to true seeds, seed pieces, suckers, corms, bulbs, fruit, tubers, grains, cuttings, cut shoots and the like and means in a preferred embodiment true seeds. The term seed treatment includes all suitable seed treatment techniques known in the art, such as seed dressing, seed coating, seed dusting, seed soaking and seed pelleting.

The present invention also relates to seeds coated with or containing the active compound of the present invention, i.e. containing a compound of formula (I), a stereoisomer, a tautomer or a salt thereof.

The term "coated with and/or containing" generally signifies that the active ingredient is for the most part on the surface of the propagation product at the time of application, although a greater or lesser part of the ingredient may penetrate into the propagation product, depending on the method of application. When the said propagation product is (re)planted, it may absorb the active ingredient.

Suitable seed is seed of cereals, root crops, oil crops, vegetables, spices, ornamentals, for example seed of durum and other wheat, barley, oats, rye, maize (fodder maize and sugar maize / sweet and field corn), soybeans, oil crops, crucifers, cotton, sunflowers, bananas, rice, oilseed rape, turnip rape, sugarbeet, fodder beet, eggplants, potatoes, grass, lawn, turf, fodder grass, tomatoes, leeks, pumpkin/squash, cabbage, iceberg lettuce, pepper, cucumbers, melons, Brassica species, melons, beans, peas, garlic, onions, carrots, tuberous plants such as potatoes, sugar cane, tobacco, grapes, petunias, geranium/pelargoniums, pansies and impatiens.

In addition, the compounds of formula (I), including the tautomers and stereoisomers, as well as their salts, may also be used for the treatment seeds from plants, which tolerate the action of herbicides or fungicides or insecticides owing to breeding, including genetic

engineering methods.

For example, the compounds of formula (I), including the tautomers and stereoisomers, as well as their salts, can be employed in treatment of seeds from plants, which are resistant to herbicides from the group consisting of the sulfonylureas, imidazolinones, glufosinate- ammonium or glyphosate-isopropylammonium and analogous active substances (see for example, EP-A-0242236, EP-A-242246) (WO 92/00377) (EP-A-0257993, U.S. Pat. No.

5,013,659) or in transgenic crop plants, for example cotton, with the capability of producing Bacillus thuringiensis toxins (Bt toxins) which make the plants resistant to certain pests (EP-A- 0142924, EP-A-0193259),

Furthermore, the compounds of formula (I), including the tautomers and stereoisomers, as well as their salts, can be used also for the treatment of seeds from plants, which have modified characteristics in comparison with existing plants consist, which can be generated for example by traditional breeding methods and/or the generation of mutants, or by recombinant

procedures). For example, a number of cases have been described of recombinant modifications of crop plants for the purpose of modifying the starch synthesized in the plants (e.g. WO 92/1 1376, WO 92/14827, WO 91/19806) or of transgenic crop plants having a modified fatty acid composition (WO 91/13972).

The seed treatment application of the active compound is carried out by spraying or by dusting the seeds before sowing of the plants and before emergence of the plants.

Compositions which are especially useful for seed treatment are e.g.:

A Soluble concentrates (SL, LS)

D Emulsions (EW, EO, ES)

E Suspensions (SC, OD, FS)

F Water-dispersible granules and water-soluble granules (WG, SG)

G Water-dispersible powders and water-soluble powders (WP, SP, WS)

H Gel-Formulations (GF)

I Dustable powders (DP, DS)

Conventional seed treatment formulations include for example flowable concentrates FS, solutions LS, powders for dry treatment DS, water dispersible powders for slurry treatment WS, water-soluble powders SS and emulsion ES and EC and gel formulation GF. These

formulations can be applied to the seed diluted or undiluted. Application to the seeds is carried out before sowing, either directly on the seeds or after having pregerminated the latter

In a preferred embodiment a FS formulation is used for seed treatment. Typcially, a FS formulation may comprise 1 -800 g/l of active ingredient, 1 -200 g/l Surfactant, 0 to 200 g/l antifreezing agent, 0 to 400 g/l of binder, 0 to 200 g/l of a pigment and up to 1 liter of a solvent, preferably water.

Especially preferred FS formulations of a compound of formula (I), a stereoisomer, a tautomer or a salt, for seed treatment usually comprise from 0.1 to 80% by weight (1 to 800 g/l) of the the compound of formula (I), including its tautomers and stereoisomers, or a salt thereof, from 0.1 to 20 % by weight (1 to 200 g/l) of at least one surfactant, e.g. 0.05 to 5 % by weight of a wetter and from 0.5 to 15 % by weight of a dispersing agent, up to 20 % by weight, e.g. from 5 to 20 % of an anti-freeze agent, from 0 to 15 % by weight, e.g. 1 to 15 % by weight of a pigment and/or a dye, from 0 to 40 % by weight, e.g. 1 to 40 % by weight of a binder (sticker /adhesion agent), optionally up to 5 % by weight, e.g. from 0.1 to 5 % by weight of a thickener, optionally from 0.1 to 2 % of an anti-foam agent, and optionally a preservative such as a biocide, antioxidant or the like, e.g. in an amount from 0.01 to 1 % by weight and a filler/vehicle up to 100 % by weight.

Seed Treatment formulations may additionally also comprise binders and optionally colorants. Binders can be added to improve the adhesion of the active materials on the seeds after treatment. Suitable binders are homo- and copolymers from alkylene oxides like ethylene oxide or propylene oxide, polyvinylacetate, polyvinylalcohols, polyvinylpyrrolidones, and copolymers thereof, ethylene-vinyl acetate copolymers, acrylic homo- and copolymers, polyethyleneamines, polyethyleneamides and polyethyleneimines, polysaccharides like celluloses, tylose and starch, polyolefin homo- and copolymers like olefin/maleic anhydride copolymers, polyurethanes, polyesters, polystyrene homo and copolymers

Optionally, also colorants can be included in the formulation. Suitable colorants or dyes for seed treatment formulations are Rhodamin B, C.I. Pigment Red 1 12, C.I. Solvent Red 1 , pigment blue 15:4, pigment blue 15:3, pigment blue 15:2, pigment blue 15:1 , pigment blue 80, pigment yellow 1 , pigment yellow 13, pigment red 1 12, pigment red 48:2, pigment red 48:1 , pigment red 57:1 , pigment red 53:1 , pigment orange 43, pigment orange 34, pigment orange 5, pigment green 36, pigment green 7, pigment white 6, pigment brown 25, basic violet 10, basic violet 49, acid red 51 , acid red 52, acid red 14, acid blue 9, acid yellow 23, basic red 10, basic red 108.

Examples of a gelling agent is carrageen (Satiagel ^® )

In the treatment of seed, the application rates of the compounds of formula (I) are generally from 0.1 g to 10 kg per 100 kg of seed, preferably from 1 g to 5 kg per 100 kg of seed, more preferably from 1 g to 1000 g per 100 kg of seed and in particular from 1 g to 200 g per 100 kg of seed.

The invention therefore also relates to seed comprising a compound of the formula (I), a tautomer, a stereoisomer or an agriculturally useful salt thereof, as defined herein. The amount of the compound of the formula (I) or the agriculturally useful salt thereof will in general vary from 0.1 g to 10 kg per 100 kg of seed, preferably from 1 g to 5 kg per 100 kg of seed, in particular from 1 g to 1000 g per 100 kg of seed. For specific crops such as lettuce the rate can be higher.

The compounds of formula (I), including their stereoisomers and their tautomers, and the veterinarily acceptable salts thereof are in particular also suitable for being used for combating parasites in and on animals.

An object of the present invention is therfore also to provide new methods to control parasites in and on animals. Another object of the invention is to provide safer pesticides for animals. Another object of the invention is further to provide pesticides for animals that may be used in lower doses than existing pesticides. And another object of the invention is to provide pesticides for animals, which provide a long residual control of the parasites. The invention also relates to compositions containing a parasiticidally effective amount of a compound of formula (I) or a stereoisomer or a tautomer or a veterinarily acceptable salt thereof and an acceptable carrier, for combating parasites in and on animals.

The present invention also provides a method for treating, controlling, preventing and protecting animals against infestation and infection by parasites, which comprises orally, topically or parenterally administering or applying to the animals a parasiticidally effective amount of a compound of formula (I) or a stereoisomer or a tautomer or a veterinarily acceptable salt thereof or a composition comprising it.

The invention also provides a process for the preparation of a composition for treating, controlling, preventing or protecting animals against infestation or infection by parasites which comprises a parasiticidally effective amount of a compound of formula (I) or a stereoisomer or a tautomer or a veterinarily acceptable salt thereof or a composition comprising it.

Activity of compounds against agricultural pests does not suggest their suitability for control of endo- and ectoparasites in and on animals which requires, for example, low, non- emetic dosages in the case of oral application, metabolic compatibility with the animal, low toxicity, and a safe handling.

Surprisingly it has now been found that compounds of formula (I), including their stereoisomers and tautomers, and the salts thereof, are suitable for combating endo- and ectoparasites in and on animals.

Compounds of formula (I), including their stereoisomers and their tautomers, and the veterinarily acceptable salts thereof, and compositions comprising them are preferably used for controlling and preventing infestations and infections animals including warm-blooded animals, including humans, and fish. They are for example suitable for controlling and preventing infestations and infections in mammals such as cattle, sheep, swine, camels, deer, horses, pigs, poultry, rabbits, goats, dogs and cats, water buffalo, donkeys, fallow deer and reindeer, and also in fur-bearing animals such as mink, chinchilla and raccoon, birds such as hens, geese, turkeys and ducks and fish such as fresh- and salt-water fish such as trout, carp and eels.

Compounds of formula (I), including their stereoisomers and their tautomers, and the veterinarily acceptable salts thereof and compositions comprising them are preferably used for controlling and preventing infestations and infections in domestic animals, such as dogs or cats.

Infestations in warm-blooded animals and fish include, but are not limited to, lice, biting lice, ticks, nasal bots, keds, biting flies, muscoid flies, flies, myiasitic fly larvae, chiggers, gnats, mosquitoes and fleas.

The compounds of formula (I), including their stereoisomers and their tautomers, and the veterinarily acceptable salts thereof and compositions comprising them are suitable for systemic and/or non-systemic control of ecto- and/or endoparasites. They are active against all or some stages of development.

The compounds of formula (I) including their stereoisomers and their tautomers, and the veterinarily acceptable salts thereof are especially useful for combating ectoparasites.

The compounds of formula (I), including their stereoisomers and their tautomers, and the veterinarily acceptable salts thereof are especially useful for combating parasites of the following orders and species, respectively:

fleas (Siphonaptera), e.g. Ctenocephalides felis, Ctenocephalides cams, Xenopsylla cheopis, Pulex irritans, Tunga penetrans, and Nosopsyllus fasciatus;

cockroaches (Blattaria - Blattodea), e.g. Blattella germanica, Blattella asahinae,

Periplaneta americana, Periplaneta japonica, Periplaneta brunnea, Periplaneta fuligginosa, Periplaneta australasiae, and Blatta orientalis;

flies, mosquitoes (Diptera), e.g. Aedes aegypti, Aedes albopictus, Aedes vexans,

Anastrepha ludens, Anopheles maculipennis, Anopheles crucians, Anopheles albimanus, Anopheles gambiae, Anopheles freeborni, Anopheles leucosphyrus, Anopheles minimus,

Anopheles quadrimaculatus, Calliphora vicina, Chrysomya bezziana, Chrysomya hominivorax, Chrysomya macellaria, Chrysops discalis, Chrysops silacea, Chrysops atlanticus, Cochliomyia hominivorax, Cord y lob ia anthropophaga, Culicoides furens, Culex pipiens, Culex nig ri palpus, Culex quinquefasciatus, Culex tarsalis, Culiseta inornata, Culiseta melanura, Dermatobia hominis, Fannia canicularis, Gasterophilus intestinalis, Glossina morsitans, Glossina palpalis, Glossina fuscipes, Glossina tachinoides, Haematobia irritans, Haplodiplosis equestris,

Hippelates spp., Hypoderma lineata, Leptoconops torrens, Lucilia caprina, Lucilia cuprina, Lucilia sericata, Lycoria pectoralis, Mansonia spp., Musca domestica, Muscina stabulans, Oestrus ovis, Phlebotomus argentipes, Psorophora columbiae, Psorophora discolor,

Prosimulium mixtum, Sarcophaga haemorrhoidalis, Sarcophaga sp., Simulium vittatum,

Stomoxys calcitrans, Tabanus bovinus, Tabanus atratus, Tabanus lineola, and Tabanus similis; lice (Phthiraptera), e.g. Pediculus humanus capitis, Pediculus humanus corporis, Pthirus pubis, Haematopinus eurysternus, Haematopinus suis, Linognathus vituli, Bovicola bovis, Menopon gallinae, Menacanthus stramineus and Solenopotes capillatus;

ticks and parasitic mites (Parasitiformes): ticks (Ixodida), e.g. Ixodes scapularis, Ixodes holocyclus, Ixodes pacificus, Rhiphicephalus sanguineus, Dermacentor andersoni, Dermacentor variabilis, Amblyomma americanum, Ambryomma maculatum, Ornithodorus hermsi,

Ornithodorus turicata and parasitic mites (Mesostigmata), e.g. Ornithonyssus bacoti and Dermanyssus gallinae; Actinedida (Prostigmata) und Acaridida (Astigmata) e.g. Acarapis spp., Cheyletiella spp., Omithocheyletia spp., Myobia spp., Psorergates spp., Demodex spp., Trombicula spp.,

Listrophorus spp., Acarus spp., Tyrophagus spp., Caloglyphus spp., Hypodectes spp.,

Pterolichus spp., Psoroptes spp., Chorioptes spp., Otodectes spp., Sarcoptes spp., Notoedres spp.,Knemidocoptes spp., Cytodites spp., and Laminosioptes spp;

Bugs (Heteropterida): Cimex lectularius, Cimex hemipterus, Reduvius senilis, Triatoma spp., Rhodnius ssp., Panstrongylus ssp. and Arilus critatus;

Anoplurida, e.g. Haematopinus spp., Linognathus spp., Pediculus spp., Phtirus spp., and Solenopotes spp.;

Mallophagida (suborders Arnblycerina and Ischnocerina), e.g. Trimenopon spp., Menopon spp., Trinoton spp., Bovicola spp., Wemeckiella spp., Lepikentron spp., Trichodectes spp., and Felicola spp;

Roundworms Nematoda:

Wipeworms and Trichinosis (Trichosyringida), e.g. Trichinellidae (Trichinella spp.), (Trichuridae Trichuris spp., Capillaria spp.;

Rhabditida, e.g. Rhabditis spp, Strongyloides spp., Helicephalobus spp;

Strongylida, e.g. Strongylus spp., Ancylostoma spp., Necator americanus, Bunostomum spp. (Hookworm), Trichostrongylus spp., Haemonchus contortus., Ostertagia spp. , Cooperia spp., Nematodirus spp., Dictyocaulus spp., Cyathostoma spp., Oesophagostomum spp., Stephanurus dentatus, Ollulanus spp., Chabertia spp., Stephanurus dentatus , Syngamus trachea, Ancylostoma spp., Uncinaria spp., Globocephalus spp., Necator spp., Metastrongylus spp., Muellerius capillaris, Protostrongylus spp., Angiostrongylus spp., Parelaphostrongylus spp. Aleurostrongylus abstrusus, and Dioctophyma renale;

Intestinal roundworms (Ascaridida), e.g. Ascaris lumbricoides, Ascaris suum, Ascaridia galli, Parascaris equorum, Enterobius vermicularis (Threadworm), Toxocara canis, Toxascaris leonine, Skrjabinema spp., and Oxyuris equi;

Camallanida, e.g. Dracunculus medinensis (guinea worm);

Spirurida, e.g. Thelazia spp. Wuchereria spp., Brugia spp., Onchocerca spp., Dirofilari spp.a, Dipetalonema spp., Setaria spp., Elaeophora spp., Spirocerca lupi, and Habronema spp.;

Thorny headed worms (Acanthocephala), e.g. Acanthocephalus spp.,

Macracanthorhynchus hirudinaceus and Oncicola spp;

Planarians (Plathelminthes):

Flukes (Trematoda), e.g. Faciola spp., Fascioloides magna, Paragonimus spp.,

Dicrocoelium spp., Fasciolopsis buski, Clonorchis sinensis, Schistosoma spp., Trichobilharzia spp., Alaria alata, Paragonimus spp., and Nanocyetes spp; Cercomeromorpha, in particular Cestoda (Tapeworms), e.g. Diphyllobothrium spp., Tenia spp., Echinococcus spp., Dipylidium caninum, Multiceps spp., Hymenolepis spp.,

Mesocestoides spp., Vampirolepis spp., Moniezia spp., Anoplocephala spp., Sirometra spp., Anoplocephala spp., and Hymenolepis spp.

The compounds of formula (I), including their stereoisomers and their tautomers, and the salts thereof and compositions containing them are particularly useful for the control of pests from the orders Diptera, Siphonaptera and Ixodida.

Moreover, the use of the compounds of formula (I), including their stereoisomers and their tautomers, and the salts thereof and compositions containing them for combating mosquitoes is especially preferred.

The use of the compounds of formula (I), including their stereoisomers and their tautomers, and the salts thereof and compositions containing them for combating flies is a further preferred embodiment of the present invention.

Furthermore, the use of the compounds of formula (I), including their stereoisomers and their tautomers, and the salts thereof and compositions containing them for combating fleas is especially preferred.

The use of the compounds of formula (I), including their stereoisomers and their tautomers, and the salts thereof and compositions containing them for combating ticks is a further preferred embodiment of the present invention.

The compounds of formula (I), including their stereoisomers and their tautomers, and the salts thereof also are especially useful for combating endoparasites (roundworms nematoda, thorny headed worms and planarians).

Administration can be carried out both prophylactically and therapeutically.

Administration of the active compounds is carried out directly or in the form of suitable preparations, orally, topically/dermally or parenterally.

For oral administration to warm-blooded animals, the compounds of the present invention may be formulated as animal feeds, animal feed premixes, animal feed concentrates, pills, solutions, pastes, suspensions, drenches, gels, tablets, boluses and capsules. In addition, the compounds of the present invention may be administered to the animals in their drinking water. For oral administration, the dosage form chosen should provide the animal with 0.01 mg/kg to 100 mg/kg of animal body weight per day of the formula (I) compound, preferably with 0.5 mg/kg to 100 mg/kg of animal body weight per day.

Alternatively, the compounds of the present invention may be administered to animals parenterally, for example, by intraruminal, intramuscular, intravenous or subcutaneous injection. The compounds of the present invention may be dispersed or dissolved in a physiologically acceptable carrier for subcutaneous injection. Alternatively, the compounds of the present invention may be formulated into an implant for subcutaneous administration. In addition the compounds of the present invention may be transdermally administered to animals. For parenteral administration, the dosage form chosen should provide the animal with 0.01 mg/kg to 100 mg/kg of animal body weight per day of a compound of the present invention.

The compounds of the present invention may also be applied topically to the animals in the form of dips, dusts, powders, collars, medallions, sprays, shampoos, spot-on and pour-on formulations and in ointments or oil-in-water or water-in-oil emulsions. For topical application, dips and sprays usually contain 0.5 ppm to 5,000 ppm and preferably 1 ppm to 3,000 ppm of the compounds of the present invention. In addition, the compounds of the present invention may be formulated as ear tags for animals, particularly quadrupeds such as cattle and sheep.

Suitable preparations are:

Solutions such as oral solutions, concentrates for oral administration after dilution, solutions for use on the skin or in body cavities, pouring-on formulations, gels;

- Emulsions and suspensions for oral or dermal administration; semi-solid preparations;

Formulations in which the active compound is processed in an ointment base or in an oil-in- water or water-in-oil emulsion base;

Solid preparations such as powders, premixes or concentrates, granules, pellets, tablets, boluses, capsules; aerosols and inhalants, and active compound-containing shaped articles.

Compositions suitable for injection are prepared by dissolving the active ingredient in a suitable solvent and optionally adding further ingredients such as acids, bases, buffer salts, preservatives, and solubilizers. The solutions are filtered and filled sterile.

Suitable solvents are physiologically tolerable solvents such as water, alkanols such as ethanol, butanol, benzyl alcohol, glycerol, propylene glycol, polyethylene glycols, N-methyl- pyrrolidone, 2-pyrrolidone, and mixtures thereof.

The compounds of the present invention can optionally be dissolved in physiologically tolerable vegetable or synthetic oils which are suitable for injection.

Suitable solubilizers are solvents which promote the dissolution of the active compound in the main solvent or prevent its precipitation. Examples are polyvinylpyrrolidone, polyvinyl alcohol, polyoxyethylated castor oil, and polyoxyethylated sorbitan ester.

Suitable preservatives are benzyl alcohol, trichlorobutanol, p-hydroxybenzoic acid esters, and n-butanol.

Oral solutions are administered directly. Concentrates are administered orally after prior dilution to the use concentration. Oral solutions and concentrates are prepared according to the state of the art and as described above for injection solutions, sterile procedures not being necessary.

Solutions for use on the skin are trickled on, spread on, rubbed in, sprinkled on or sprayed on.

Solutions for use on the skin are prepared according to the state of the art and according to what is described above for injection solutions, sterile procedures not being necessary.

Further suitable solvents are polypropylene glycol, phenyl ethanol, phenoxy ethanol, ester such as ethyl or butyl acetate, benzyl benzoate, ethers such as alkyleneglycol alkylether, e.g. dipropylenglycol monomethylether, ketons such as acetone, methylethylketone, aromatic hydrocarbons, vegetable and synthetic oils, dimethylformamide, dimethylacetamide, transcutol, solketal, propylencarbonate, and mixtures thereof.

It may be advantageous to add thickeners during preparation. Suitable thickeners are inorganic thickeners such as bentonites, colloidal silicic acid, aluminium monostearate, organic thickeners such as cellulose derivatives, polyvinyl alcohols and their copolymers, acrylates and methacrylates.

Gels are applied to or spread on the skin or introduced into body cavities. Gels are prepared by treating solutions which have been prepared as described in the case of the injection solutions with sufficient thickener that a clear material having an ointment-like consistency results. The thickeners employed are the thickeners given above.

Pour-on formulations are poured or sprayed onto limited areas of the skin, the active compound penetrating the skin and acting systemically.

Pour-on formulations are prepared by dissolving, suspending or emulsifying the active compound in suitable skin-compatible solvents or solvent mixtures. If appropriate, other auxiliaries such as colorants, bioabsorption-promoting substances, antioxidants, light stabilizers, adhesives are added.

Suitable solvents are, for example, water, alkanols, glycols, polyethylene glycols, polypropylene glycols, glycerol, aromatic alcohols such as benzyl alcohol, phenylethanol, phenoxyethanol, esters such as ethyl acetate, butyl acetate, benzyl benzoate, ethers such as alkylene glycol alkyl ethers such as dipropylene glycol monomethyl ether, diethylene glycol mono-butyl ether, ketones such as acetone, methyl ethyl ketone, cyclic carbonates such as propylene carbonate, ethylene carbonate, aromatic and/or aliphatic hydrocarbons, vegetable or synthetic oils, DMF, dimethylacetamide, n-alkylpyrrolidones such as methylpyrrolidone, n- butylpyrrolidone or n-octylpyrrolidone, N-methylpyrrolidone, 2-pyrrolidone, 2,2-dimethyl-4-oxy- methylene-1 ,3-diox- olane and glycerol formal. Suitable colorants are all colorants permitted for use on animals and which can be dissolved or suspended.

Suitable absorption-promoting substances are, for example, DMSO, spreading oils such as isopropyl myristate, dipropylene glycol pelargonate, silicone oils and copolymers thereof with polyethers, fatty acid esters, triglycerides, fatty alcohols.

Suitable antioxidants are, for example, sulfites or metabisulfites such as potassium metabisulfite, ascorbic acid, butylhydroxytoluene, butylhydroxyanisole, tocopherol.

Suitable light stabilizers are, for example, novantisolic acid.

Suitable adhesives are, for example, cellulose derivatives, starch derivatives,

polyacrylates, natural polymers such as alginates, gelatin.

Emulsions can be administered orally, dermally or as injections.

Emulsions are either of the water-in-oil type or of the oil-in-water type.

They are prepared by dissolving the active compound either in the hydrophobic or in the hydrophilic phase and homogenizing this with the solvent of the other phase with the aid of suitable emulsifiers and, if appropriate, other auxiliaries such as colorants, absorption-promoting substances, preservatives, antioxidants, light stabilizers, viscosity-enhancing substances.

Suitable hydrophobic phases (oils) are, for example: liquid paraffins, silicone oils, natural vegetable oils such as sesame oil, almond oil, castor oil, synthetic triglycerides such as caprylic/capric biglyceride, triglyceride mixture with vegetable fatty acids of the chain length Cs- Ci2 or other specially selected natural fatty acids, partial glyceride mixtures of saturated or unsaturated fatty acids possibly also containing hydroxyl groups, mono- and diglycerides of the Cs-C-io fatty acids, fatty acid esters such as ethyl stearate, di-n-butyryl adipate, hexyl laurate, dipropylene glycol perlargonate, esters of a branched fatty acid of medium chain length with saturated fatty alcohols of chain length C16-C18, isopropyl myristate, isopropyl palmitate, caprylic/capric acid esters of saturated fatty alcohols of chain length C12-C18, isopropyl stearate, oleyl oleate, decyl oleate, ethyl oleate, ethyl lactate, waxy fatty acid esters such as synthetic duck coccygeal gland fat, dibutyl phthalate, diisopropyl adipate, and ester mixtures related to the latter, fatty alcohols such as isotridecyl alcohol, 2-octyldodecanol, cetylstearyl alcohol, oleyl alcohol, and fatty acids such as oleic acid and mixtures thereof.

Suitable hydrophilic phases are, for example, water, alcohols such as propylene glycol, glycerol, sorbitol and mixtures thereof.

Suitable emulsifiers are, for example,

non-ionic surfactants, e.g. polyethoxylated castor oil, polyethoxylated sorbitan monooleate, sorbitan monostearate, glycerol monostearate, polyoxyethyl stearate, alkylphenol polyglycol ether; ampholytic surfactants such as di-sodium N-lauryl-p-iminodipropionate or lecithin; anionic surfactants, such as sodium lauryl sulfate, fatty alcohol ether sulfates, mono/dialkyl polyglycol ether orthophosphoric acid ester monoethanolamine salt; cation-active surfactants, such as cetyltrimethylammonium chloride.

Suitable further auxiliaries are substances which enhance the viscosity and stabilize the emulsion, such as carboxymethylcellulose, methylcellulose and other cellulose and starch derivatives, polyacrylates, alginates, gelatin, gum arabic, polyvinylpyrrolidone, polyvinyl alcohol, copolymers of methyl vinyl ether and maleic anhydride, polyethylene glycols, waxes, colloidal silicic acid or mixtures of the substances mentioned.

Suspensions can be administered orally or topically/dermally. They are prepared by suspending the active compound in a suspending agent, if appropriate with addition of other auxiliaries such as wetting agents, colorants, bioabsorption-promoting substances,

preservatives, antioxidants, light stabilizers.

Liquid suspending agents are all homogeneous solvents and solvent mixtures.

Suitable wetting agents (dispersants) are the emulsifiers given above.

Other auxiliaries, which may be mentioned, are those given above.

Semi-solid preparations can be administered orally or topically/dermally. They differ from the suspensions and emulsions described above only by their higher viscosity.

For the production of solid preparations, the active compound is mixed with suitable excipients, if appropriate with addition of auxiliaries, and brought into the desired form.

Suitable excipients are all physiologically tolerable solid inert substances. Those used are inorganic and organic substances. Inorganic substances are, for example, sodium chloride, carbonates such as calcium carbonate, hydrogencarbonates, aluminium oxides, titanium oxide, silicic acids, argillaceous earths, precipitated or colloidal silica, or phosphates. Organic substances are, for example, sugar, cellulose, foodstuffs and feeds such as milk powder, animal meal, grain meals and shreds, starches.

Suitable auxiliaries are preservatives, antioxidants, and/or colorants which have been mentioned above.

Other suitable auxiliaries are lubricants and glidants such as magnesium stearate, stearic acid, talc, bentonites, disintegration-promoting substances such as starch or crosslinked polyvinylpyrrolidone, binders such as starch, gelatin or linear polyvinylpyrrolidone, and dry binders such as microcrystalline cellulose.

In general, "parasiticidally effective amount" means the amount of active ingredient needed to achieve an observable effect on growth, including the effects of necrosis, death, retardation, prevention, and removal, destruction, or otherwise diminishing the occurrence and activity of the target organism. The parasiticidally effective amount can vary for the various compounds/compositions used in the invention. A parasiticidally effective amount of the compositions will also vary according to the prevailing conditions such as desired parasiticidal effect and duration, target species, mode of application, and the like.

The compositions which can be used in the invention can comprise generally from about

0.001 to 95% of a compound of formula (I), a stereoisomer, a tautomer or a salt thereof.

Generally it is favorable to apply the compounds of the present invention in total amounts of 0.5 mg/kg to 100 mg/kg per day, preferably 1 mg/kg to 50 mg/kg per day.

Ready-to-use preparations contain the compounds acting against parasites, preferably ectoparasites, in concentrations of 10 ppm to 80 per cent by weight, preferably from 0.1 to 65 per cent by weight, more preferably from 1 to 50 per cent by weight, most preferably from 5 to 40 per cent by weight.

Preparations which are diluted before use contain the compounds acting against ectoparasites in concentrations of 0.5 to 90 per cent by weight, preferably of 1 to 50 per cent by weight.

Furthermore, the preparations for controlling endoparasites comprise a compound of the present invention usually in concentrations of 10 ppm to 2 per cent by weight, preferably of 0.05 to 0.9 per cent by weight, very particularly preferably of 0.005 to 0.25 per cent by weight.

In a preferred embodiment of the present invention, the compositions comprising the a compound of the present invention are applied dermally / topically.

In a further preferred embodiment, the topical application is conducted in the form of compound-containing shaped articles such as collars, medallions, ear tags, bands for fixing at body parts, and adhesive strips and foils.

Generally it is favorable to apply solid formulations which release compounds of the present invention in total amounts of 10 mg/kg to 300 mg/kg, preferably 20 mg/kg to 200 mg/kg, most preferably 25 mg/kg to 160 mg/kg body weight of the treated animal in the course of three weeks.

For the preparation of the shaped articles, thermoplastic and flexible plastics as well as elastomers and thermoplastic elastomers are used. Suitable plastics and elastomers are polyvinyl resins, polyurethane, polyacrylate, epoxy resins, cellulose, cellulose derivatives, polyamides and polyester which are sufficiently compatible with the compounds of the present invention. A detailed list of plastics and elastomers as well as preparation procedures for the shaped articles is given e.g. in WO 03/086075.

The present invention is now illustrated in further details by the following examples, without imposing any limitation thereto. The following abbreviations are used:

TFA: trifluoroacetic acid

EtOAc: ethyl acetate

HPLC: High Performance Liquid Chromatography

MS: Mass spectrometry

MeOH: Methanol

t.R = retention time

The compound examples were characterized by coupled High Performance Liquid Chromatography with mass spectrometry (HPLC/MS) or by their melting point.

Method A: Analytical HPLC column 1 : RP-18 column Chromolith Speed ROD (from Merck KgaA, Germany). Elution: acetonitrile + 0.1 % TFA acid/ water + 0.1 % TFA in a ratio of from 5:95 to 95:5 in 5 minutes at 40 °C.

Method B:

Analytical UPLC column: Phenomenex Kinetex 1 ,7 μηι XB-C18 100A; 50 x 2.1 mm;

mobile phase: A: water+ 0.1 % TFA; B: acetonitrile + 0.1 % TFA; gradient: 5-100% B in 1.50 minutes; 100% B 0.20 min; flow: 0,8-1 ,0mL/min in 1 ,50 minutes at 60°C.

MS-method: ESI positive. A. Preparation examples

1 . Preparation of intermediate compounds

1 .1 Synthesis of amine salt E1.1

(E1.1)

A solution of 2-chloro-5-chloromethyl (16.20 g, 100 mmol) and 2-amino-pyridine (9.60 g, 102 mmol) in ethanol (100 mL) was refluxed for 24 hours. The reaction was then cooled to room temperature, and concentrated in vacuo. Then 100 mL of toluene were added to the residue, and the mixture was concentrated in vacuo. 75 mL of CH2CI2 were added to the residue and the mixture was stirred rapidly for 15 minutes, during which time a precipitate forms. The precipitate was then filtered, and washed with CH2CI2 (50 mL), diethyl ether (50 mL), and dried under vacuum to afford the title product as a pale yellow solid (14.0g, 55% yield). LC-MS: mass calc'd. for C11 H11CIN3 [M] ⁺ 220.1 , found 220.1 ; t _R = 0.529 min.

Example 1 : (Compound example E1.2; compound of formula I, wherein Het is 6- chloropyridin-3-yl, -W -W ² -W ³ -W ⁴ - represent -CH=CH-CH=CH-, X is O, D is CHCH ₃ , R ³ and R ⁴ are CH ₃ , Y is O)

To a suspension of amine salt E1.1 (0.200g, 0.781 mmol), 2- (isopropylideneamino)oxypropanoic acid (4.45, 30.06 mmol), and triethylamine (0.147g, 1.01 mmol) in 1 ,2-dichloroethane (3 mL) at room temperature was added a solution of propyl phosphoric anhydride (0.400g, 1 .25 mmol, a 50% wt solution in EtOAc was used). The reaction was then heated in a mircrowave oven at 90°C for 3 hrs. The obtained reaction mixture was then dilluted with EtOAc (150 mL) and the organic phase was washed with saturated aqueous NHCO3 (100 mL) and water (100mL). The layers were separated, and the organic layer was dried over Na2S0 ₄ and concentrated in vacuo to afford a residue, which was purified using column chromatography over silica gel (0->70% MeOH/ChbC ) to afford the desired product as a beige solid (0.101 g, 37% yield).

LC-MS: mass calc'd. for C17H20N4O2CI [M+H] ⁺ 347.1 , found 347.1 ; t _R = 0.752 min. The following compounds of formula l-A.1 a, where R ¹ is hydrogen,

were prepared in analogy to the method described in example 1 and are listed in table B including their physico-chemical data. Table B also lists the physico-chemical data of the compound example E1 .2 prepared in example 1 . Table B:

Ex. Example

4-CI-C6H ₄ : 4-chlorophenyl B Biological Examples

The biological activity of the compounds of formula I of the present invention may be evaluated in biological tests as described in the following.

General conditions: If not otherwise specified, most test solutions are to be prepared as follows: The active compound is to be dissolved at the desired concentration in a mixture of 1 :1 (vohvol) distilled watenacteon. Further, the test solutions are to be prepared at the day of use (and, if not otherwised specified, in general at concentrations wt/vol).

B.1 Green Peach Aphid (Myzus persicae)

For evaluating control of green peach aphid (Myzus persicae) through systemic means, the test unit consists of 96-well-microtiter plates containing liquid artificial diet under an artificial membrane.

The compounds are formulated using a solution containing 75% v/v water and 25% v/v DMSO. Different concentrations of formulated compounds are pipetted into the aphid diet, using a custom built pipetter, at two replications.

After application, 5 - 8 adult aphids are placed on the artificial membrane inside the microtiter plate wells. The aphids are then allowed to suck on the treated aphid diet and incubated at about 23 + 1 °C and about 50 + 5 % relative humidity for 3 days. Aphid mortality and fecundity is then visually assessed. In this test, compounds E1.2, E1 .3, E1.4, E1.5, E1 .6, E1 .7, E1.8, E1.9, E1 .10 and E1.1 1 at 800 ppm showed at least 75% mortality in comparison with untreated controls.

B.2 Vetch aphid {Megoura viciae)

The active compounds were formulated in 3:1 (vohvol) water : DMSO with different concentrations of formulated compounds.

Bean leaf disks were placed into microtiterplates filled with 0.8% agar-agar and 2.5 ppm OPUS™. The leaf disks were sprayed with 2.5 μΙ of the test solution and 5 to 8 adult aphids were placed into the microtiter plates which were then closed and kept at 23 ± 1 °C and 50 ± 5% relative humidity under fluorescent light for 6 days. Mortality was assessed on the basis of vital, reproduced aphids. Aphid mortality and fecundity was then visually assessed.

In this test, compounds E1.2, E1 .3, E1.4, E1.5, E1 .6, E1.7, E1 .8, E1.9, E1.10 and E1 .1 1 at 800 ppm showed at least 75% mortality in comparison with untreated controls.

B.3 Cotton aphid (Aphis gossypii)

(a) The active compound is dissolved at the desired concentration in a mixture of 1 :1 (vohvol) distilled water : acetone. Surfactant (Alkamuls® EL 620) is added at a rate of 0.1 % (vol/vol). The test solution is prepared at the day of use.

Potted cowpea plants are colonized with approximately 50 - 100 aphids of various stages by manually transferring a leaf tissue cut from infested plant 24 hours before application. Plants are sprayed after the pest population has been recorded. Treated plants are maintained on light carts at about 28°C. Percent mortality is assessed after 72 hours.

In this test, compound E1 .2 at 300 ppm showed at least 75 % mortality in comparison with untreated controls.

(b) The active compounds were formulated in cyclohexanone as a 10,000 ppm solution supplied in 1 .3 ml ABgene® tubes. These tubes were inserted into an automated electrostatic sprayer equipped with an atomizing nozzle and they served as stock solutions for which lower dilutions were made in 1 : 1 (vohvol) water : aceton. A nonionic surfactant (Kinetic®) was included in the solution at a volume of 0.01 % (v/v).

Cotton plants at the cotyledon stage were infested with aphids prior to treatment by placing a heavily infested leaf from the main aphid colony on top of each cotyledon. Aphids were allowed to transfer overnight to accomplish an infestation of 80-100 aphids per plant and the host leaf was removed. The infested plants were then sprayed by an automated electrostatic plant sprayer equipped with an atomizing spray nozzle. The plants were dried in the sprayer fume hood, removed from the sprayer, and then maintained in a growth room under fluorescent lighting in a 24-hr photoperiod at 25°C and 20-40% relative humidity. Aphid mortality on the treated plants, relative to mortality on untreated control plants, was determined after 5 days.

In this test, compounds E1 .4, E1.5, E1 .6, E1.8 and E1.9 at 300 ppm showed at least 75% mortality in comparison with untreated controls.

B.4 Cowpea aphid {Aphis craccivora)

The active compound is dissolved at the desired concentration in a mixture of 1 :1 (vohvol) distilled water : acetone. Surfactant (Alkamuls® EL 620) is added at a rate of 0.1 % (vol/vol). The test solution is prepared at the day of use.

Potted cowpea plants are colonized with approximately 50 - 100 aphids of various stages by manually transferring a leaf tissue cut from infested plant 24 hours before application. Plants are sprayed after the pest population has been recorded. Treated plants are maintained on light carts at about 28°C. Percent mortality is assessed after 72 hours.

In this test, compound E1.2, E1.3, E1 .4, E1 .5, E1.6, E1.7, E1 .8, E1 .9 and E1 .10 at 500 ppm showed at least 75 % mortality in comparison with untreated controls.

B.5 Orchid thrips (dichromothrips corbetti)

Dichromothrips corbetti adults used for bioassay are obtained from a colony maintained continuously under laboratory conditions. For testing purposes, the test compound is diluted in a 1 :1 mixture of acetone:water (vohvol), plus 0.01 % vol/vol Alkamuls ^® EL 620 surfactant.

Thrips potency of each compound is evaluated by using a floral-immersion technique.

Plastic petri dishes are used as test arenas. All petals of individual, intact orchid flowers are dipped into treatment solution and allowed to dry. Treated flowers are placed into individual petri dishes along with about 20 adult thrips. The petri dishes are then covered with lids. All test arenas are held under continuous light and a temperature of about 28°C for duration of the assay. After 3 days, the numbers of live thrips are counted on each flower, and along inner walls of each petri dish. The percent mortality is recorded 72 hours after treatment.

In this test, compounds E1.2, E1.4, E1 .5, E1.8 and E1.9 at 500 ppm showed at least 75 % mortality in comparison with untreated controls. B.6 Rice green leafhopper (Nephotettix virescens) Rice seedlings are cleaned and washed 24 hours before spraying. The active compounds are formulated in 50:50 acetone:water (vohvol), and 0.1 % vol/vol surfactant (EL 620) is added. Potted rice seedlings are sprayed with 5 ml. test solution, air dried, placed in cages and inoculated with 10 adults. Treated rice plants are kept at about 28-29°C and relative humidity of about 50-60%. Percent mortality is recorded after 72 hours.

In this test, compounds E1.2, E1.3, E1 .4, E1 .5, E1.6, E1.7, E1 .8 and E1.9 at 500 ppm showed at least 75 % mortality in comparison with untreated controls.

B.7 Rice brown plant hopper (Nilaparvata lugens)

Rice seedlings are cleaned and washed 24 hours before spraying. The active compounds is formulated in 50:50 acetone:water (vohvol) and 0.1 % vol/vol surfactant (EL 620) was added. Potted rice seedlings are sprayed with 5 ml test solution, air dried, placed in cages and inoculated with 10 adults. Treated rice plants are kept at about 28-29°C and relative humidity of about 50-60%. Percent mortality is recorded after 72 hours.

In this test, compounds E1.2, E1.8 and E1.9 at 500 ppm showed at least 75 % mortality in comparison with untreated controls.

B.8 Boll weevil (Anthonomus grand is)

The compounds were formulated in 3:1 (vohvol) water : DMSO.

For evaluating control of boll weevil (Anthonomus grandis) the test unit consisted of 24- well-microtiter plates containing an insect diet and 20-30 A. grandis eggs. Different

concentrations of formulated compounds were sprayed onto the insect diet at 20 μΙ, using a custom built micro atomizer, at two replications. After application, the microtiter plates were incubated at 23 ± 1 °C and 50 ± 5 % relative humidity for 5 days. Egg and larval mortality was then visually assessed.

In this test, compounds E1.2, E1 .3, E1.4, and E1.6 at 800 ppm showed at least 75% mortality in comparison with untreated controls

B.9 Mediterranean fruitfly (Ceratitis capitata)

For evaluating control of Mediterranean fruitfly (Ceratitis capitata) the test unit consists of microtiter plates containing an insect diet and 50-80 C. capitata eggs.

The compounds are formulated using a solution containing 75% v/v water and 25% v/v DMSO. Different concentrations of formulated compounds are sprayed onto the insect diet at 5 μΙ, using a custom built micro atomizer, at two replications. After application, microtiter plates are incubated at about 28 + 1 °C and about 80 + 5 % relative humidity for 5 days. Egg and larval mortality is then visually assessed.

In this test, compounds E1 .4 and E1 .5 at 2500 ppm showed at least 75 % mortality in comparison with untreated controls.

B.10 Tobacco budworm (Heliothis virescens)

For evaluating control of tobacco budworm (Heliothis virescens) the test unit consisted of 96-well-microtiter plates containing an insect diet and 15-25 H. virescens eggs.

The compounds were formulated using a solution containing 75% v/v water and 25% v/v DMSO. Different concentrations of formulated compounds were sprayed onto the insect diet at 10 μΙ, using a custom built micro atomizer, at two replications.

After application, microtiter plates were incubated at about 28 + 1 °C and about 80 + 5 % relative humidity for 5 days. Egg and larval mortality was then visually assessed.

In this test, compounds E1.2, E1.3, and E1.4 at 2500 ppm showed at least 75 % mortality in comparison with untreated controls.

B.1 1 Silverleaf whitefly (Bemisia argentifolii) (adults)

The active compounds were formulated in cyclohexanone as a 10,000 ppm solution supplied in tubes. The tubes were inserted into an automated electrostatic sprayer equipped with an atomizing nozzle and they served as stock solutions for which lower dilutions were made in 50% acetone:50% water (v/v). A nonionic surfactant (Kinetic®) was included in the solution at a volume of 0.01 % (v/v).

Cotton plants at the cotyledon stage (one plant per pot) were sprayed by an automated electrostatic plant sprayer equipped with an atomizing spray nozzle. The plants were dried in the sprayer fume hood and then removed from the sprayer. Each pot was pla-ced into a plastic cup and about 10 to 12 whitefly adults (approximately 3-5 days old) were introduced. The insects were collected using an aspirator and a nontoxic Tygon® tubing connected to a barrier pipette tip. The tip, containing the collected insects, was then gently inserted into the soil containing the treated plant, allowing insects to crawl out of the tip to reach the foliage for feeding. Cups were covered with a reusable screened lid. Test plants were maintained in a growth room at about 25°C and about 20-40% relative humidity for 3 days, avoiding direct exposure to fluorescent light (24 hour photoperiod) to prevent trapping of heat inside the cup. Mortality was assessed 3 days after treatment, compared to untreated control plants.

B.12 Green Soldier Stink Bug (Nezara viridula) The active compound is dissolved at the desired concentration in a mixture of 1 :1 (vohvol) distilled water : aceteone. Surfactant (Kinetic HV) is added at a rate of 0.01 % (vol/vol).The test solution is prepared at the day of use.

Soybean pods were placed in microwavable plastic cups lined with moist filter paper and inoculated with ten 3rd instar N. viridula. Using a hand atomizer, approximately 2 ml solution is sprayed into each cup. Treated cups were kept at about 28-29°C and relative humidity of about 50-60%. Percent mortality was recorded after 5 days.