Pyridine ketones useful as herbicides

Description

The present invention relates to novel herbicidally active pyridine ketones, to processes for their preparation, to compositions which comprise these compounds, and to their use for controlling weeds, in particular in crops of useful plants, or for inhibiting plant growth.

Pyridine ketones having herbicidal action are described, for example, in WO 97/46530. We have now found novel pyridine ketones having herbicidal and growth-inhibiting properties.

The present invention thus provides compounds of the formula I

in which

each R independently is C

1

-C

6

alkyl, C

2

-C

6

alkenyl, C

2

-C

6

haloalkenyl, C

2

-C

6

alkynyl, C

2

-C

6

haloalkynyl, C

3

-C

6

cycloalkyl, C

1

-C

6

alkoxy, C

1

-C

6

haloalkoxy, C

1

-C

6

alkylthio, C

1

-C

6

alkylsulfinyl, C

1

-C

6

alkylsulfonyl, C

1

-C

6

haloalkyl, C

1

-C

6

haloalkylthio, C

1

-C

6

haloalkylsulfinyl, C

1

-C

6

haloalkylsulfonyl, C

1

-C

6

alkoxycarbonyl, C

1

-C

6

alkylcarbonyl, C

1

-C

6

alkylamino, di-C

1

-C

6

alkylamino, C

1

-C

6

alkylaminosulfonyl, di-C

1

-C

6

alkylaminosulfonyl, —N(R

1

)—S—R

2

, —N(R

3

)—SO—R

4

, —N(R

5

)—SO

2

—R

6

, nitro, cyano, halogen, hydroxy, amino, formyl, hydroxy-C

1

-C

6

alkyl, C

1

-C

6

alkoxy-C

1

-C

6

alkyl, C

1

-C

6

alkoxycarbonyloxy-C

1

-C

6

alkyl, C

1

-C

6

alkylthio-C

1

-C

6

alkyl, C

1

-C

6

alkylsulfinyl-C

1

-C

6

alkyl, C

1

-C

6

alkylsulfonyl-C

1

-C

6

alkyl, thiocyanato-C

1

-C

6

alkyl, cyano-C

1

-C

6

alkyl, oxiranyl, C

3

-C

6

alkenyloxy, C

3

-C

6

alkynyloxy, C

1

-C

6

alkoxy-C

1

-C

6

alkoxy, cyano-C

1

-C

6

alkenyloxy, C

1

-C

6

alkoxycarbonyloxy-C

1

-C

6

alkoxy, C

3

C

6

alkynyloxy, cyano-C

1

-C

6

alkoxy, C

1

-C

6

alkoxycarbonyl-C

1

-C

6

alkoxy, C

1

-C

6

alkylthio-C

1

-C

6

alkoxy, alkoxycarbonyl-C

1

-C

6

alkylthio, alkoxycarbonyl-C

1

-C

6

alkylsulfinyl, alkoxycarbonyl-C

1

-C

6

alkylsulfonyl, C

1

-C

6

alkylsulfonyloxy, C

1

-C

6

haloalkylsulfonyloxy, phenyl, benzyl, phenoxy, phenylthio, phenylsulfinyl, phenylsulfonyl, benzylthio, benzylsulfinyl or benzylsulfonyl, where the phenyl groups may be mono- or polysubstituted by halogen, methyl, ethyl, trifluoromethyl, methoxy or nitro, or R is a five- to ten-membered monocyclic or fused bicyclic ring system, which may be aromatic or partially saturated and may contain 1 to 4 heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur, where the ring system is either attached directly to the pyridine ring or attached to the pyridine ring via a C

1

-C

4

alkylene group, and where each ring system may not contain more than 2 oxygen atoms and not more than two sulfur atoms, and where the ring system for its part may be mono-, di- or trisubstituted by C

1

-C

6

alkyl, C

1

-C

6

haloalkyl, C

3

-C

6

alkenyl, C

3

-C

6

haloalkenyl, C

3

-C

6

alkynyl, C

3

-C

6

haloalkynyl, C

1

-C

6

alkoxy, C

1

-C

6

haloalkoxy, C

3

-C

6

alkenyloxy, C

3

-C

6

alkynyloxy, mercapto, C

1

-C

6

alkylthio, C

1

-C

6

haloalkylthio, C

3

-C

6

alkenylthio, C

3

-C

6

haloalkenylthio, C

3

-C

6

alkynylthio, C

2

-C

5

alkoxyalkylthio, C

3

-C

5

acetylalkylthio, C

3

-C

6

alkoxycarbonylalkylthio, C

2

-C

4

cyanoalkylthio, C

1

-C

6

alkylsulfinyl, C

1

-C

6

haloalkylsulfinyl, C

1

-C

6

alkylsulfonyl, C

1

-C

6

haloalkylsulfonyl, aminosulfonyl, C

1

-C

6

alkylaminosulfonyl, C

1

-C

6

dialkylaminosulfonyl, C

1

-C

6

alkylene-R

7

, NR

8

R

9

, halogen, cyano, nitro, phenyl and benzylthio, where phenyl and benzylthio for their part may be substituted on the phenyl ring by C

1

-C

3

alkyl, C

1

-C

3

haloalkyl, C

1

-C

3

alkoxy, C

1

-C

3

haloalkoxy, halogen, cyano or nitro, and where substituents on the nitrogen in the heterocyclic ring are different from halogen;

m is 1, 2, 3 or 4;

p is 0 or 1;

R

1

, R

3

and R

5

independently of one another are hydrogen or C

1

-C

6

alkyl;

R

2

is NR

10

R

11

, C

1

-C

6

alkoxy, C

1

-C

6

haloalkoxy, C

1

-C

6

alkyl, C

1

-C

6

haloalkyl, C

3

-C

6

alkenyl, C

3

-C

6

haloalkenyl, C

3

-C

6

alkynyl, C

3

-C

6

haloalkynyl, C

3

-C

6

cycloalkyl or phenyl, where phenyl for its part may be substituted by C

1

-C

3

alkyl, C

1

-C

6

haloalkyl, C

1

-C

6

alkoxy, C

1

-C

3

haloalkoxy, halogen, cyano or nitro;

R

4

is NR

12

R

13

, C

1

-C

6

alkoxy, C

1

-C

6

haloalkoxy, C

1

-C

6

alkyl, C

1

-C

6

haloalkyl, C

3

-C

6

alkenyl, C

3

-C

6

haloalkenyl, C

3

-C

6

alkynyl, C

3

-C

6

haloalkynyl, C

3

-C

6

cycloalkyl or phenyl, where phenyl for its part may be substituted by C

1

-C

3

alkyl, C

1

-C

3

haloalkyl, C

1

-C

3

alkoxy, C

1

-C

3

haloalkoxy, halogen, cyano or nitro;

R

6

is NR

14

R

15

, C

1

-C

6

alkoxy, C

1

-C

6

haloalkoxy, C

1

-C

6

alkyl, C

1

-C

6

haloalkyl, C

3

-C

6

alkenyl, C

3

-C

6

haloalkenyl, C

3

-C

6

alkynyl, C

3

-C

6

haloalkynyl, C

3

-C

6

cycloalkyl or phpnyl, where phenyl for its part may be substituted by C

1

-C

3

alkyl, C

1

-C

3

haloalkyl, C

1

-C

3

alkoxy, C

1

-C

3

haloalkoxy, halogen, cyano or nitro;

R

7

is C

1

-C

3

alkoxy, C

2

-C

4

alkoxycarbonyl, C

1

-C

3

alkylthio, C

1

-C

3

alkylsulfinyl, C

1

-C

3

alkylsulfonyl or phenyl, where phenyl for its part may be substituted by C

1

-C

3

alkyl, C

1

-C

3

haloalkyl, C

1

-C

3

alkoxy, C

1

-C

3

haloalkoxy, halogen, cyano or nitro;

R

8

, R

10

, R

12

and R

14

independently of one another are hydrogen or C

1

-C

6

alkyl;

R

9

, R

11

, R

13

and R

15

is independently of one another are C

1

-C

6

alkyl or C

1

-C

6

alkoxy;

Q is the group Q

1

in which

R

16

, R

17

, R

18

and R

19

independently of one another are hydrogen, hydroxyl, C

1

-C

4

alkyl, C

2

-C

6

alkenyl, C

2

-C

6

alkynyl, C

1

-C

4

alkoxycarbonyl, C

1

-C

6

alkylthio, C

1

-C

6

alkylsulfinyl, C

1

-C

6

alkylsulfonyl, C

1

-C

4

alkyl-NHS(O)

2

, C

1

-C

4

haloalkyl, —NH—C

1

-C

4

alkyl, —N(C

1

-C

4

alkyl)

2

, C

1

-C

6

alkoxy, cyano, nitro, halogen or phenyl, which for its part may be substituted by C

1

-C

4

alkyl, C

1

-C

4

haloalkyl, C

1

-C

4

alkoxy, C

1

-C

4

haloalkoxy, C

1

-C

4

alkylcarbonyl, C

1

-C

4

alkoxycarbonyl, amino, C

1

-C

4

alkylamino, di-C

1

-C

4

alkylamino, C

1

-C

6

alkylthio, C

1

-C

6

alkylsulfinyl, C

1

-C

6

alkylsulfonyl, C

1

-C

4

alkyl-S(O)

2

O, C

1

-C

4

haloalkylthio, C

1

-C

4

haloalkylsulfinyl, C

1

-C

4

haloalkylsulfonyl, C

1

-C

4

haloalkyl-S(O)

2

O, C

1

-C

4

alkyl-S(O)

2

NH, C

1

-C

4

alkyl-S(O)

2

N(C

1

-C

4

alkyl), halogen, nitro, COOH or cyano; or two adjacent substituents from the group consisting of R

16

, R

17

, R

18

and R

19

form a C

2

-C

6

alkyiene bridge;

R

20

is hydroxyl, O

−

M

+

, halogen, cyano, SCN, OCN, C

1

-C

12

alkoxy, C

1

-C

4

alkoxycarbonyl-C

1

-C

4

alkoxy, C

1

-C

12

alkylthio, C

1

-C

12

alkylsulfinyl, C

1

-C

12

alkylsulfonyl, C

1

-C

12

haloalkylthio, C

1

-C

12

haloalkylsulfinyl, C

1

-C

12

haloalkylsulfonyl, C

1

-C

6

alkoxy-C

1

-C

6

alkylthio, C

1

-C

6

alkoxy-C

1

-C

6

alkylsulfinyl, C

1

-C

6

alkoxy-C

1

-C

6

alkylsulfonyl, C

2

-C

12

alkenylthio, C

2

-C

12

alkeny isulfinyl, C

2

-C

12

alkenylsulfonyl, C

2

-C

12

alkynylthio, C

2

-C

12

alkynylsulfinyl, C

2

-C

12

alkynylsulfonyl, C

2

-C

12

haloalkenylthio, C

2

-C

12

haloalkenylsulfinyl, C

2

-C

12

haloalkenylsulfonyl, C

1

-C

4

alkoxycarbonyl-C

1

-C

4

alkylthio, C

1

-C

4

alkoxycarbonyl-C

1

-C

4

alkylsulfinyl, C

1

-C

4

alkoxycarbonyl-C

1

-C

4

alkylsulfonyl, (C

1

-C

4

alkoxy)

2

P(O)O, C

1

-C

4

alkyl-(C

1

-C

4

alkoxy)P(Q)O, H(C

1

-C

4

alkoxy)P(O)O,

R

37

R

38

N, R

71

R

72

NNH—, R

73

R

74

NC(O)NH—, C

1

-C

4

alkyl-S(O)

39

, C

1

-C

4

haloalkyl-S(O)

2

NR

40

, C

1

-C

6

alkyl-S(O)

2

O, C

1

-C

4

haloalkyl-S(O)

2

O, C

1

-C

18

alkylcarbonyloxy, where the alkyl group may be substituted by halogen, C

1

-C

6

alkoxy, C

1

-C

6

alkylthio or cyano, C

2

-C

18

alkenylcarbonyloxy, C

2

-C

18

alkynylcarbonyloxy, C

3

-C

6

cycloalkylcarbonyloxy, C

1

-C

12

alkoxycarbonyloxy, C

1

-C

12

alkylthiocarbonyloxy, C

1

-C

12

alkylthiocarbamoyl, C

1

-C

6

alkyl-NH(CS)N(C

1

-C

6

alkyl)—NH—, di-C

1

-C

6

alkyl-N(CS)N(C

1

-C

6

alkyl)-NH—, benzyloxy, benzylthio, benzylsulfinyl, benzyisulfonyl, phenoxy, phenylthio, phenylsulfinyl, phenylsulfonyl, phenylsulfonyloxy or benzoyloxy, where the phenyl groups for their part may each be substituted by C

1

-C

4

alkyl, C

1

-C

4

haloalkyl, C

1

-C

4

alkoxy, C

1

-C

4

haloalkoxy, C

1

-C

4

alkylcarbonyl, C

1

-C

4

alkoxycarbonyl, C

1

-C

4

alkylamino, di-C

1

-C

4

alkylamino, C

1

-C

4

alkylthio, C

1

-C

4

alkylsulfinyl, C

1

-C

4

alkylsulfonyl, C

1

-C

4

alkyl-S(O)

2

O, C

1

-C

4

haloalkylthio, C

1

-C

4

haloalkylsulfinyl, C

1

-C

4

haloalkylsulfonyl, C

1

-C

4

haloalkyl-S(O)

2

O, C

1

-C

4

alkyl-S(O)

2

NH, C

1

-C

4

alkyl-S(O)

2

N(C

1

-C

4

alkyl), halogen, nitro or cyano,

or a group Ar

1

-thio, Ar

2

-sulfinyl, Ar

3

-sulfonyl, —OCO—Ar

4

or NH—Ar

s

in which Ar

1

, Ar

2

, Ar

3

, Ar

4

and Ar

5

independently of one another are a five- to ten-membered monocyclic or fused bicyclic ring system which may be aromatic or partially saturated and may contain 1 to 4 heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur, and in which each ring system may not contain more than 2 oxygen atoms and not more than two sulfur atoms, and in which the ring system for its part may be mono-, di- or trisubstituted by C

1

-C

6

alkyl, C

1

-C

6

haloalkyl, C

3

-C

6

alkenyl, C

3

-C

6

haloalkenyl, C

3

-C

6

alkynyl, C

3

-C

6

haloalkynyl, C

1

-C

6

alkoxy, C

1

-C

6

haloalkoxy, C

3

-C

6

alkenyloxy, C

3

-C

6

alkynyloxy, mercapto, C

1

-C

6

alkylthio, C

1

-C

6

haloalkylthio, C

3

-C

6

alkenylthio, C

3

-C

6

haloalkenylthio, C

3

-C

6

alkynylthio, C

2

-C

5

alkoxyalkylthio, C

3

-C

5

acetylalkylthio, C

3

-C

6

alkoxycarbonylalkylthio, C

2

-C

4

cyanoalkylthio, C

1

-C

6

alkylsulfinyl, C

1

-C

6

haloalkylsulfinyl, C

1

-C

6

alkylsulfonyl, C

1

-C

6

haloalkylsulfonyl, aminosulfonyl, C

1

-C

2

alkylaminosufonyl, C

2

-C

4

dialkylaminosulfonyl, C

1

-C

3

alkylene-R

41

, NR

42

R

43

, halogen, cyano, nitro, phenyl and benzylthio, where phenyl and benzylthio for their part may be substituted on the phenyl ring by C

1

-C

3

alkyl, C

1

-C

3

haloalkyl, C

1

-C

3

alkoxy, C

1

-C

3

haloalkoxy, halogen, cyano or nitro, and where substituents on the nitrogen in the heterocyclic ring are different from halogen;

R

41

is C

1

-C

3

alkoxy, C

2

-C

4

alkoxycarbonyl, C

1

-C

3

alkylthio, C

1

-C

3

alkylsulfinyl, C

1

-C

3

alkylsulfonyl or phenyl, where phenyl for its part may be substituted by C

1

-C

3

alkyl, C

1

-C

3

haloalkyl, C

1

-C

3

alkoxy, C

1

-C

3

haloalkoxy, halogen, cyano or nitro;

R

42

is hydrogen or C

1

-C

6

alkyl;

R

43

is C

1

-C

6

alkyl or C

1

-C

6

alkoxy;

R

21

, R

37

, R

39

, R

40

, R

71

and R

73

independently of one another are hydrogen or C

1

-C

4

alkyl;

R

22

, R

38

, R

72

and R

74

independently of one another are hydrogen, C

1

-C

12

alkyl, hydroxyl, C

1

-C

12

alkoxy, C

3

-C

6

alkenyloxy or C

3

-C

6

alkynyloxy; or R

21

and R

22

together or R

37

and R

38

together or R

71

and R

72

together or R

73

and R

74

together are pyrrolidino, piperidino, morpholino, thiomorpholino, which may be mono- or polysubstituted by methyl groups; or are the group Q

2

in which

Y is a chemical bond, an alkylene group A

1

, carbonyl, oxygen, sulfur, sulfinyl, sulfonyl, —NHR

248

or NH(CO)R

249

;

A

1

is C(R

246

R

247

)m

01

;

A is C(R

244

R

245

)r;

r and m

01

independently of one another are 1 or 2;

R

240

is hydrogen, methyl or C

1

-C

3

alkoxycarbonyl;

R

241

, R

242

, R

243

, R

244

, R

245

, R

246

and R

247

independently of one another are hydrogen, halogen or methyl, or R

243

together with an adjacent group R

245

or R

247

is a chemical bond;

R

248

and R

249

independently of one another are hydrogen or C

1

-C

4

alkyl;

R

23

is hydroxyl, O

−

M

+

, halogen, cyano, SCN, OCN, C

1

-C

12

alkoxy, C

1

-C

4

alkoxycarbonyl-C

1

-C

4

alkoxy, C

1

-C

12

alkylthio, C

1

-C

12

alkylsulfinyl, C

1

-C

12

alkylsulfonyl, C

1

-C

12

haloalkylthio, C

1

-C

12

haloalkylsulfinyl, C

1

-C

12

haloalkylsulfonyl, C

1

-C

6

alkoxy-C

1

-C

6

alkylthio, C

1

-C

6

alkoxy-C

1

-C

6

alkylsulfinyl, C

1

-C

6

alkoxy-C

1

-C

6

alkylsulfonyl, C

2

-C

12

alkenylthio, C

2

-C

12

alkenylsulfinyl, C

2

-C

12

alkenyisulfonyl, C

2

-C

12

alkynylthio, C

2

-C

12

alkynylsulfinyl, C

2

-C

12

alkynylsulfonyl, C

2

-C

12

haloalkenylthio, C

2

-C

12

haloalkenylsulfinyl, C

2

-C

12

haloalkenylsulfonyl, C

1

-C

4

alkoxycarbonyl-C

1

-C

4

alkylthio, C

1

-C

4

alkoxycarbonyl-C

1

-C

4

alkylsulfinyl, C

1

-C

4

alkoxycarbonyl-C

1

-C

4

alkylsuflonyl, (C

1

-C

4

alkoxy)

2

P(O)O, C

1

-C

4

alkyl-(C

1

-C

4

alkoxy)P(O)O, H(C

1

-C

4

alkoxy)P(O)O,

R

44

R

45

N, R

75

R

76

NNH—, R

46

R

47

NC(O)O—, R

77

R

78

NC(O)NH—, C

1

-C

4

alkyl-S(O)

2

NR

48

, C

1

-C

4

haloalkyl-S(O)

2

NR

49

, C

1

-C

4

alkyl-S(O)

2

O, C

1

-C

4

haloalkyl-S(O)

2

O, C

1

-C

18

alkylcarbonyloxy, where the alkyl group may be substituted by halogen, C

1

-C

6

alkoxy, C

1

-C

6

alkylthio or cyano, C

2

-C

18

alkenylcarbonyloxy, C

2

-C

18

alkynylcarbonyloxy, C

3

-C

6

cycloalkylcarbonyloxy, C

1

-C

12

alkoxycarbonyloxy, C

1

-C

12

alkylthiocarbonyloxy, C

1

-C

12

alkylthiocarbamoyl, C

1

-C

6

alkyl-NH(CS)N(C

1

-C

6

alkyl)—NH—, di-C

1

-C

6

alkyl-N(CS)N(C

1

-C

6

alkyl)—NH—, benzyloxy, benzylthio, benzylsulfinyl, benzylsulfonyl, phenoxy, phenylthio, phenylsulfinyl, phenyisulfonyl, phenylsulfonyloxy or benzoyloxy, where the phenyl groups for their part may each be substituted by C

1

-C

4

alkyl, C

1

-C

4

haloalkyl, C

1

-C

4

alkoxy, C

1

-C

4

haloalkoxy, C

1

-C

4

alkylcarbonyl, C

1

-C

4

alkoxycarbonyl, C

1

-C

4

alkylamino, di-C

1

-C

4

alkylamino, C

1

-C

4

alkylthio, C

1

-C

4

alkylsulfinyl, C

1

-C

4

alkylsulfonyl, C

1

-C

4

alkyl-S(O)

2

O, C

1

-C

4

haloalkylthio, C

1

-C

4

haloalkyisulfinyl, C

1

-C

4

haloalkylsulfonyl, C

1

-C

4

haloalkyl-S(O)

2

O, C

1

-C

4

alkyl-S(O)

2

NH, C

1

-C

4

alkyl-S(O)

2

N(C

1

-C

4

alkyl), halogen, nitro or cyano,

or a group Ar

6

-thio, Ar

7

-sulfinyl, Ar

8

-sulfonyl, —OCO—Ar

9

or NH—Ar

10

in which Ar

6

, Ar

7

, Ar

8

, Ar

9

and Ar

10

independently of one another are a five- to ten-membered monocyclic or fused bicyclic ring system which may be aromatic or partially saturated and may contain 1 to 4 heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur, and in which each ring system may not contain more than 2 oxygen atoms and not more than two sulfur atoms, and in which the ring system for its part may be mono-, di- or trisubstituted by C

1

-C

6

alkyl, C

1

-C

6

haloalkyl, C

3

-C

6

alkenyl, C

3

-C

6

haloalkenyl, C

3

-C

6

alkynyl, C

3

-C

6

haloalkynyl, C

1

-C

6

alkoxy, C

1

-C

6

haloalkoxy, C

3

-C

6

alkenyloxy, C

3

-C

6

alkynyloxy, mercapto, C

1

-C

6

alkylthio, C

1

-C

6

haloalkylthio, C

3

-C

6

alkenylthio, C

3

-C

6

haloalkenylthio, C

3

-C

6

alkynylthio, C

2

-C

5

alkoxyalkylthio, C

3

-C

5

acetylalkylthio, C

3

-C

6

alkoxycarbonylalkylthio, C

2

-C

4

cyanoalkylthio, C

1

-C

6

alkylsulfinyl, C

1

-C

6

haloalkylsulfinyl, C

1

-C

6

alkylsulfonyl, C

1

-C

6

haloalkylsulfonyl, aminosulfonyl, C

1

-C

2

alkylaminosulfonyl, C

2

-C

4

dialkylaminosulfonyl, C

1

-C

3

alkylene-R

50

, NR

51

R

52

, halogen, cyano, nitro, phenyl and benzylthio, where phenyl and benzylthio for their part may be substituted on the phenyl ring by C

1

-C

3

alkyl, C

1

-C

3

haloalkyl, C

1

-C

3

alkoxy, C

1

-C

3

haloalkoxy, halogen, cyano or nitro, and where substituents on the nitrogen in the heterocyclic ring are different from halogen;

R

50

is C

1

-C

3

alkoxy, C

2

-C

4

alkoxycarbonyl, C

1

-C

3

alkylthio, C

1

-C

3

alkylsulfinyl, C

1

-C

3

alkylsulfonyl or phenyl, where phenyl for its part may be substituted by C

1

-C

3

alkyl, C

1

-C

3

haloalkyl, C

1

-C

3

alkoxy, C

1

-C

3

haloalkoxy, halogen, cyano or nitro;

R

51

is hydrogen or C

1

-C

6

alkyl;

R

52

is C

1

-C

6

alkyl or C

1

-C

6

alkoxy;

R

46

, R

44

, R

48

, R

49

, R

75

and R

77

independently of one another are hydrogen or C

1

-C

4

alkyl;

R

47

, R

45

, R

76

and R

78

independently of one another are hydrogen, C

1

-C

12

alkyl, hydroxyl, C

1

-C

12

alkoxy, C

3

-C

6

alkenyloxy or C

3

-C

6

alkynyloxy; or R

44

and R

45

together or R

46

and R

47

together or R

75

and R

76

together or R

77

and R

78

together are pyrrolidino, piperidino, morpholino, thiomorpholino, which may be mono- or polysubstituted by methyl groups; or are the group Q

3

in which

R

26

is hydroxyl, O

−

M

+

, halogen, cyano, SCN, OCN, C

1

-C

12

alkoxy, C

1

-C

4

alkoxycarbonyl-C

1

-C

4

alkoxy, C

1

-C

12

alkylthio, C

1

-C

12

alkylsulfinyl, C

1

-C

12

alkylsulfonyl, C

1

-C

12

haloalkylthio, C

1

-C

12

haloalkylsulfinyl, C

1

-C

12

haloalkylsulfonyl, C

1

-C

6

alkoxy-C

1

-C

6

alkylthio, C

1

-C

6

alkoxy-C

1

-C

6

alkylsulfinyl, C

1

-C

6

alkoxy-C

1

-C

6

alkylsulfonyl, C

2

-C

12

alkenylthio, C

2

-C

12

alkenylsulfinyl, C

2

-C

12

alkenylsulfonyl, C

2

-C

12

alkynylthio, C

2

-C

12

alkynylsulfinyl, C

2

-C

12

alkynylsulfonyl, C

2

-C

12

haloalkenylthio, C

2

-C

12

haloalkenylsulfinyl, C

2

-C

12

haloalkenylsulfonyl, C

1

-C

4

alkoxycarbonyl-C

1

-C

4

alkylthio, C

1

-C

4

alkoxycarbonyl-C

1

-C

4

alkylsulfinyl, C

1

-C

4

alkoxycarbonyl-C

1

-C

4

alkylsulfonyl, (C

1

-C

4

alkoxy)

2

P(O)O, C

1

-C

4

alkyl-(C

1

-C

4

alkoxy)P(O)O, H(C

1

-C

4

alkoxy)P(O)O,

R

53

R

54

N, R

79

R

80

NNH—, R

55

R

56

NC(O)O—, R

81

R

82

NC(O)NH—, C

1

-C

4

alkyl-S(O)

2

NR

57

, C

1

-C

4

haloalkyl-S(O)

2

NR

58

, C

1

-C

4

alkyl-S(O)

2

O, C

1

-C

4

haloalkyl-S(O)

2

O, C

1

-C

18

alkylcarbonyloxy, where the alkyl group may be substituted by halogen, C

1

-C

6

alkoxy, C

1

-C

6

alkylthio or cyano, C

2

C

18

alkenylcarbonyloxy, C

2

-C

18

alkynylcarbonyloxy, C

3

-C

6

cycloalkylcarbonyloxy, C

1

-C

12

alkoxycarbonyloxy, C

1

-C

12

alkylthiocarbonyloxy, C

1

-C

12

alkylthiocarbamoyl, C

1

-C

6

alkyl-NH(CS)N(C

1

-C

6

alkyl)—NH—, di-C

1

-C

6

alkyl-N(CS)N(C

1

-C

6

alkyl)—NH—, benzyloxy, benzyithio, benzylsulfinyl, benzylsulfonyl, phenoxy, phenylthio, phenylsulfinyl, phenylsulfonyl, phenylsulfonyloxy or benzoyloxy, where the phenyl groups for their part may each be substituted by C

1

-C

4

alkyl, C

1

-C

4

haloalkyl, C

1

-C

4

alkoxy, C

1

-C

4

haloalkoxy, C

1

-C

4

alkylcarbonyl, C

1

-C

4

alkoxycarbonyl, C

1

-C

4

alkylamino, di-C

1

-C

4

alkylamino, C

1

-C

4

alkylthio, C

1

-C

4

alkylsulfinyl, C

1

-C

4

alkylsulfonyl, C

1

-C

4

alkyl-S(O)

2

O, C

1

-C

4

haloalkylthio, C

1

-C

4

haloalkylsulfinyl, C

1

-C

4

haloalkylsulfonyl, C

1

-C

4

haloalkyl-S(O)

2

O, C

1

-C

4

alkyl-S(O)

2

NH, C

1

-C

4

alkyl-S(O)

2

N(C

1

-C

4

alkyl), halogen, nitro or cyano,

or a group Ar

11

-thio, Ar

12

-sulfinyl, Ar

13

-sulfonyl, —OCO—Ar

14

or NH—Ar

15

in which Ar

11

, Ar

12

, Ar

13

, Ar

14

and Ar

15

independently of one another are a five- to ten-membered monocyclic or fused bicyclic ring system which may be aromatic or partially saturated and may contain 1 to 4 heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur, and in which each ring system may not contain more than 2 oxygen atoms and not more than two sulfur atoms, and in which the ring system for its part may be mono-, di- or trisubstituted by C

1

-C

6

alkyl, C

1

-C

6

haloalkyl, C

3

-C

6

alkenyl, C

3

-C

6

haloalkenyl, C

3

-C

6

alkynyl, C

3

-C

6

haloalkynyl, C

1

-C

6

alkoxy, C

1

-C

6

haloalkoxy, C

3

-C

6

alkenyloxy, C

3

-C

6

alkynyloxy, mercapto, C

1

-C

6

alkylthio, C

1

-C

6

haloalkylthio, C

3

-C

6

alkenylthio, C

3

-C

6

haloalkenylthio, C

3

-C

6

alkynylthio, C

2

-C

5

alkoxyalkylthio, C

3

-C

5

acetylalkylthio, C

3

-C

6

alkoxycarbonylalkylthio, C

2

-C

4

cyanoalkylthio, C

1

-C

6

alkylsulfinyl, C

1

-C

6

haloalkylsulfinyl, C

1

-C

6

alkylsulfonyl, C

1

-C

6

haloalkylsulfonyl, aminosulfonyl, C

1

-C

2

alkylaminosulfonyl, C

2

-C

4

dialkylaminosulfonyl, C

1

-C

3

alkylene-R

59

, NR

60

R

61

, halogen, cyano, nitro, phenyl and benzylthio, where phenyl and benzylthio for their part may be substituted on the phenyl ring by C

1

-C

3

alkyl, C

1

-C

3

haloalkyl, C

1

-C

3

alkoxy, C

1

-C

3

haloalkoxy, halogen, cyano or nitro, and where substituents on the nitrogen in the heterocyclic ring are different from halogen;

R

59

is C

1

-C

3

alkoxy, C

2

-C

4

alkoxycarbonyl, C

1

-C

3

alkylthio, C

1

-C

3

alkylsulfinyl, C

1

-C

3

alkylsulfonyl or phenyl, where phenyl for its part may be substituted by C

1

-C

3

alkyl, C

1

-C

3

haloalkyl, C

1

-C

3

alkoxy, C

1

-C

3

haloalkoxy, halogen, cyano or nitro;

R

60

is hydrogen or C

1

-C

6

alkyl;

R

61

is C

1

-C

6

alkyl or C

1

-C

6

alkoxy;

R

55

, R

53

, R

57

, R

58

, R

79

and R

81

independently of one another are hydrogen or C

1

-C

4

alkyl;

R

56

, R

54

, R

80

and R

82

independently of one another are hydrogen, C

1

-C

12

alkyl, hydroxyl, C

1

-C

12

alkoxy, C

3

-C

6

alkenyloxy or C

3

-C

6

alkynyloxy; or R

53

and R

54

together or R

55

and R

56

together or R

79

and R

80

together or R

81

and R

82

together are pyrrolidino, piperidino, morpholino, thiomorpholino, which may be mono- or polysubstituted by methyl groups;

R

29

is hydrogen, C

1

-C

6

alkyl, C

1

-C

4

alkylcarbonyl, C

1

-C

4

alkoxycarbonyl, (C

1

-C

4

alkyl)NHCO, phenylaminocarbonyl, benzylaminocarbonyl or (C

1

-C

4

alkyl)

2

NCO, where the phenyl and benzyl groups for their part may each be substituted by C

1

-C

4

alkyl, C

1

-C

4

haloalkyl, C

1

-C

4

alkoxy, C

1

-C

4

haloalkoxy, C

1

-C

4

alkylcarbonyl, C

1

-C

4

alkoxycarbonyl, C

1

-C

4

alkylamino, di-C

1

-C

4

alkylamino, C

1

-C

4

alkylthio, C

1

-C

4

alkylsulfinyl, C

1

-C

4

alkylsulfonyl, C

1

-C

4

alkyl-S(O)

2

O, C

1

-C

4

haloalkylthio, C

1

-C

4

haloalkylsulfinyl, C

1

-C

4

haloalkylsulfonyl, C

1

-C

4

haloalkyl-S(O)

2

O, C

1

-C

4

alkyl-S(O)

2

NH, C

1

-C

4

alkyl-S(O)

2

N(C

1

-C

4

alkyl), halogen, nitro or cyano;

or is the group Q

4

in which

R

30

is hydroxyl, O

−

M

+

, halogen, cyano, SCN, OCN, C

1

-C

12

alkoxy, C

1

-C

4

alkoxycarbonyl-C

1

-C

4

alkoxy, C

1

-C

12

alkylthio, C

1

-C

12

alkylsulfinyl, C

1

-C

12

alky lsulfonyl, C

1

-C

12

haloalkylthio, C

1

-C

12

haloalkylsulfinyl, C

1

-C

12

haloalkylsulfonyl, C

1

-C

6

alkoxy-C

1

-C

6

alkylthio, C

1

-C

6

alkoxy-C

1

-C

6

alkylsulfinyl, C

1

-C

6

alkoxy-C

1

-C

6

alkylsulfonyl, C

2

-C

12

alkenylthio, C

2

-C

12

alkenyisulfinyl, C

2

-C

12

alkenylsulfonyl, C

2

-C

12

alkynylthio, C

2

-C

12

alkynyisulfinyl, C

2

-C

12

alkynyisulfonyl, C

2

-C

12

haloalkenylthio, C

2

-C

12

haloalkenylsulfinyl, C

2

-C

12

haloalkenylsuffonyl, C

1

-C

4

alkoxycarbonyl-C

1

-C

4

alkylthio, C

1

-C

4

alkoxycarbonyl-C

1

-C

4

alkylsulfinyl, C

1

-C

4

alkoxycarbonyl-C

1

-C

4

alkylsulfonyl, (C

1

-C

4

alkoxy)

2

P(O)O, C

1

-C

4

alkyl-(C

1

-C

4

alkoxy)P(O)O, H(C

1

-C

4

alkoxy)P(O)O,

R

62

R

63

N, R

83

R

84

NNH—, R

64

R

65

NC(O)O—, R

85

R

86

NC(O)NH—, C

1

-C

4

alkyl-S(O)

2

NR

66

, C

1

-C

4

haloalkyl-S(O)

2

NR

67

, C

1

-C

4

alkyl-S(O)

2

O, C

1

-C

4

haloalkyl-S(O)

2

O, C

1

-C

18

alkylcarbonyloxy, where the alkyl group may be substituted by halogen, C

1

-C

6

alkoxy, C

1

-C

6

alkylthio or cyano, C

2

-C

18

alkenylcarbonyloxy, C

2

-C

18

alkynylcarbonyloxy, C

3

-C

6

cycloalkylcarbonyloxy, C

1

-C

12

alkoxycarbonyloxy, C

1

-C

12

alkylthiocarbonyloxy, C

1

-C

12

alkylthiocarbamoyl, C

1

-C

6

alkyl-NH(CS)N(C

1

-C

6

alkyl)NH—, di-C

1

-C

6

alkyl-N(CS)N(C

1

-C

6

alkyl)—NH—, benzyloxy, benzylthio, benzylsulfinyl, benzylsulfonyl, phenoxy, phenylthio, phenylsulfinyl, phenylsulfonyl, phenyisulfonyloxy or benzoyloxy, where the phenyl groups for their part may each be substituted by C

1

-C

4

alkyl, C

1

-C

4

haloalkyl, C

1

-C

4

alkoxy, C

1

-C

4

haloalkoxy, C

1

-C

4

alkylcarbonyl, C

1

-C

4

alkoxycarbonyl, C

1

-C

4

alkylamino, di-C

1

-C

4

alkylamino, C

1

-C

4

alkylthio, C

1

-C

4

alkylsulfinyl, C

1

-C

4

alkylsulfony l, C

1

-C

4

alkyl-S(O)

2

O, C

1

-C

4

haloalkylthio, C i-C

4

haloalkylsulfinyl, C

1

-C

4

haloalkylsulfonyl, C

1

-C

4

haloalkyl-S(O)

2

O, C

1

-C

4

alkyl-S(O)

2

NH, C

1

-C

4

alkyl-S(O)

2

N(C

1

-C

4

alkyl), halogen, nitro or cyano,

or a group Ar

16

-thio, Ar

17

-sulfinyl, Ar

18

-sulfonyl, —OCO—Ar

19

or NH—Ar

20

in which Ar

16

, Ar

17

, Ar

18

, Ar

19

and Ar

20

independently of one another are a five- to ten-membered monocyclic or fused bicyclic ring system which may be aromatic or partially saturated and may contain 1 to 4 heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur, and in which each ring system may not contain more than 2 oxygen atoms and not more than two sulfur atoms, and in which the ring system for its part may be mono-, di- or trisubstituted by C

1

-C

6

alkyl, C

1

-C

6

haloalkyl, C

3

-C

6

alkenyl, C

3

-C

6

haloalkenyl, C

3

-C

6

alkynyl, C

3

-C

6

haloalkynyl, C

1

-C

6

alkoxy, C

1

-C

6

haloalkoxy, C

3

-C

6

alkenyloxy, C

3

-C

6

alkynyloxy, mercapto, C

1

-C

6

alkylthio, C

1

-C

6

haloalkylthio, C

3

-C

6

alkenylthio, C

3

-C

6

haloalkenylthio, C

3

-C

6

alkynylthio, C

2

-C

5

alkoxyalkylthio, C

3

-C

5

acety oalkylthio, C

3

-C

6

alkoxycarbonylalkylthio, C

2

-C

4

cyanoalkylthio, C

1

-C

6

alkylsulfinyl, C

1

-C

6

haloalkylsulfinyl, C

1

-C

6

alkylsulfonyl, C

1

-C

6

haloalkylsulfonyl, aminosulfonyl, C

1

-C

2

alkylaminosulfony l, C

2

-C

4

dialkylaminosulfonyl, C

1

-C

3

alkylene-R

68

, NR

69

R

70

, halogen, cyano, nitro, phenyl and benzylthio, where phenyl and benzylthio for their part may be substituted on the phenyl ring by C

1

-C

3

alkyl, C

1

-C

3

haloalkyl, C

1

-C

3

alkoxy, C

1

-C

3

haloalkoxy, halogen, cyano or nitro, and where substituents on the nitrogen in the heterocyclic ring are different from halogen;

R

68

is C

1

-C

3

alkoxy, C

2

-C

4

alkoxycarbonyl, C

1

-C

3

alkylthio, C

1

-C

3

alkylsulfinyl, C

1

-C

3

alkylsulfonyl or phenyl, where phenyl for its part may be substituted by C

1

-C

3

alkyl, C

1

-C

3

haloalkyl, C

1

-C

3

alkoxy, C

1

-C

3

haloalkoxy, halogen, cyano or nitro;

R

70

is hydrogen or C

1

-C

6

alkyl;

R

61

is C

1

-C

6

alkyl or C

1

-C

6

alkoxy;

R

64

, R

62

, R

66

, R

67

, R

83

and R

85

independently of one another are hydrogen or C

1

-C

4

alkyl;

R

65

, R

63

, R

84

and R

86

independently of one another are hydrogen, C

1

-C

12

alkyl, hydroxyl, C

1

-C

12

alkoxy, C

3

-C

6

alkenyloxy or C

3

-C

6

alkynyloxy; or R

62

and R

63

together or R

64

and R

65

together or R

83

and R

84

together or R

85

and R

86

together are pyrrolidino, piperidino, morpholino, thiomorpholino, which may be mono- or polysubstituted by methyl groups;

R

33

and R

34

independently of one another are hydrogen, C

1

-C

4

alkyl, C

2

-C

6

alkenyl, C

2

-C

6

alkynyl, C

1

-C

4

alkoxycarbonyl, C

1

-C

6

alkylthio, C

1

-C

6

alkylsulfinyl, C

1

-C

6

alkylsulfonyl, C

1

-C

4

alkyl-NHS(O)

2

, C

1

-C

4

haloalkyl, —NH—C

1

-C

4

alkyl, —N(C

1

-C

4

alkyl)

2

, C

1

-C

6

alkoxy or phenyl, which for its part may be substituted by C

1

-C

4

alkyl, C

1

-C

4

haloalkyl, C

1

-C

4

alkoxy, C

1

-C

4

haloalkoxy, C

1

-C

4

alkylcarbonyl, C

1

-C

4

alkoxycarbonyl, amino, C

1

-C

4

alkylamino, di-C

1

-C

4

alkylamino, C

1

-C

6

alkylthio, C

1

-C

6

alkylsulfinyl, C

1

-C

6

alkylsulfonyl, C

1

-C

4

alkyl-S(O)

2

O, C

1

-C

4

haloalkylthio, C

1

-C

4

haloalkylsulfinyl, C

1

-C

4

haloalkylsulfonyl, C

1

-C

4

haloalkyl-S(O)

2

O, C

1

-C

4

alkyl-S(O)

2

NH, C

1

-C

4

alkyl-S(O)

2

N(C

1

-C

4

alkyl), halogen, nitro, COOH or cyano; or R

33

and R

34

together form a C

2

-C

6

alkylene bridge; and

R

35

is hydrogen, C

1

-C

6

alkyl, C

3

-C

6

alkenyl, C

3

-C

6

alkynyl or benzyl, which for its part may be substituted by halogen, methyl or methoxy, or is C

1

-C

4

alkoxycarbonyl or phenyl, which for its part may be substituted by C

1

-C

4

alkyl, C

1

-C

4

haloalkyl, C

1

-C

4

aikoxy, C

1

-C

4

haloalkoxy, C

1

-C

4

alkylcarbonyl, C

1

-C

4

alkoxycarbonyl, amino, C

1

-C

4

alkylamino, di-C

1

-C

4

alkylamino, C

1

-C

4

alkylthio, C

1

-C

4

alkylsulfinyl, C

1

-C

4

alkylsulfonyl, C

1

-C

4

alkyl-S(O)

2

O, C

1

-C

4

haloalkylthio, C

1

-C

4

haloalkylsulfinyl, C

1

-C

4

haloalkylsuifonyl, C

1

-C

4

haloalkyl-S(O)

2

O, C

1

-C

4

alkyl-S(O)

2

NH, C

1

-C

4

alkyl-S(O)

2

N(C

1

-C

4

alkyl), halogen, nitro, COOH or cyano;

or is the group Q

5

in which

Z is S, SO or SO

2

;

R

01

is hydrogen, C

1

-C

8

alkyl, C

1

-C

8

alkyl substituted by halogen, C

1

-C

4

alkoxy, C

1

-C

4

alkylthio, C

1

-C

4

alkylsulfonyl, C

1

-C

4

alkylsulfinyl, —CO

2

R

02

, —COR

03

, —COSR

04

, —NR

05

R

06

, CONR

036

R

037

or phenyl, which for its part may be substituted by C

1

-C

4

alkyl, C

1

-C

6

haloalkyl, C

1

-C

4

alkoxy, C

1

-C

4

haloalkoxy, C

2

-C

6

alkenyl, C

3

-C

6

alkynyl, C

3

-C

6

alkenyloxy, C

3

-C

6

alkynyloxy, halogen, nitro, cyano, —COOH, COOC

1

-C

4

alkyl, COOphenyl, C

1

-C

4

alkoxy, phenoxy, (C

1

-C

4

alkoxy)-C

1

-C

4

alkyl, (C

1

-C

4

alkylthio)-C

1

-C

4

alkyl, (C

1

-C

4

alkylsulfinyl)-C

1

-C

4

alkyl, (C

1

-C

4

alkylsulfonyl)-C

1

-C

4

alkyl, NHS)

2

—C

1

-C

4

alkyl, NHSO

2

-phenyl, N(C

1

-C

6

alkyl)S)

2

—C

1

-C

4

alkyl, N(C

1

-C

6

alkyl)SO

2

-phenyl, N(C

2

-C

6

alkenyl)S)

2

—C

1

-C

4

alkyl, N(C

2

-C

6

alkenyl)SO

2

-phenyl, N(C

3

-C

6

alkynyl)SO

2

—C

1

-C

4

alkyl, N(C

3

-C

6

alkynyl)SO

2

-phenyt, N(C

3

-C

7

cycloalkyl)SO

2

—C

1

-C

4

alkyl, N(C

3

-C

7

cycloalkyl)SO

2

-phenyl, N(phenyl)SO

2

—C

1

-C

4

alkyl, N(phenyl)SO

2

-phenyl, OSO

2

—C

1

-C

4

alkyl, CONR

25

R

26

, OSO

2

—C

1

-C

4

haloalkyl, OSO

2

-phenyl, C

1

-C

4

alkylthio, C

1

-C

4

haloalkylthio, phenytthio, C

1

-C

4

alkylsulfonyl, C

1

-C

4

haloalkylsulfonyl, phenylsulfonyl, C

1

-C

4

alkylsulfinyl, C

1

-C

4

haloalkylsulfinyl, phenylsulfinyl, C

1

-C

4

alkylene-phenyl or —NR

015

CO

2

R

027

;

or R

01

is C

2

-C

8

alkenyl or C

2

-C

8

alkenyl substituted by halogen, C

1

-C

4

alkoxy, C

1

-C

4

alkylthio, C

1

-C

4

alkylsulfonyl, C

1

-C

4

alkylsulfinyl, —CONR

032

R

033

, cyano, nitro, —CHO, —CO

2

R

038

, —COR

039

, —COS—C

1

-C

4

alkyl, —NR

034

R

035

or phenyl which for its part may be substituted by C

1

-C

4

alkyl, C

1

-C

6

haloalkyl, C

1

-C

4

alkoxy, C

1

-C

4

haloalkoxy, C

2

-C

6

alkenyl, C

3

-C

6

alkynyl, C

3

-C

6

alkenyloxy, C

3

-C

6

alkynyloxy, halogen, nitro, cyano, —COOH, COOC

1

-C

4

alkyl, COOphenyl, C

1

-C

4

alkoxy, phenoxy, (C

1

-C

4

alkoxy)-C

1

-C

4

alkyl, (C

1

-C

4

alkylthio)-C

1

-C

4

alkyl, (C

1

-C

4

alkylsulfinyl)-C

1

-C

4

alkyl, (C

1

-C

4

alkylsulfonyl)-C

1

-C

4

alkyl, NHSO)

2

—C

1

-C

4

alkyl, NHSO

2

-phenyl, N(C

1

-C

6

alkyl)SO

2

—C

1

-C

4

alkyl, N(C

1

-C

6

alkyl)SO

2

-phenyl, N(C

2

-C

6

alkenyl)SO

2

—C

1

-C

4

alkyl, N(C

2

-C

6

alkenyl)SO

2

-phenyl, N(C

3

-C

6

alkynyl)SO

2

—C

1

-C

4

alkyl, N(C

3

-C

6

alkynyl)SO

2

-phenyl, N(C

3

-C

7

cycloalkyl)SO

2

—C

1

-C

4

alkyl, alkyl, N(C

3

-C

7

cycloalkyl)SO

2

-phenyl, N(phenyl)SO

2

—C

1

-C

4

alkyl, N(phenyl)SO

2

-phenyl, OSO

2

—C

1

-C

4

alkyl, CONR

040

R

041

, OSO

2

—C

1

-C

4

haloalkyl, OSO

2

-phenyl, C

1

-C

4

alkylthio, C

1

-C

4

haloalkylthio, phenylthio, C

1

-C

4

alkylsulfonyl, C

1

-C

4

haloalkylsulfonyl, phenylsulfonyl, C

1

-C

4

alkylsulfinyl, C

1

-C

4

haloalkylsulfinyl, phenylsuffinyl, C

1

-C

4

alkylene-phenyl or —NR

043

CO

2

R

042

;

or R

01

is C

3

-C

6

alkynyl or C

3

-C

6

alkynyl substituted by halogen, C

1

-C

4

haloalkyl, cyano, —CO

2

R

044

or phenyl, which for its part may be substituted by C

1

-C

4

alkyl, C

1

-C

6

haloalkyl, C

1

-C

4

alkoxy, C

1

-C

4

haloalkoxy, C

2

-C

6

alkenyl, C

3

-C

6

alkynyl, C

3

-C

6

alkenyloxy, C

3

-C

6

alkynyloxy, halogen, nitro, cyano, —COOH, COOC

1

-C

4

alkyl, COOphenyl, C

1

-C

4

alkoxy, phenoxy, (C

1

-C

4

alkoxy)-C

1

-C

4

alkyl, (C

1

-C

4

alkylthio)-C

1

-C

4

alkyl, (C

1

-C

4

alkylsulfinyl)-C

1

-C

4

alkyl, (C

1

-C

4

alkylsulfonyl)-C

1

-C

4

alkyl, NHSO

2

—C

1

-C

4

alkyl, NHSO

2

-phenyl, N(C

1

-C

6

alkyl)SO

2

—C

1

-C

4

alkyl, N(C

1

-C

6

alkyl)SO

2

-phenyl, N(C

2

-C

6

alkenyl)SO

2

—C

1

-C

4

alkyl, N(C

2

-C

6

alkenyl)SO

2

-phenyl, N(C

3

-C

6

alkynyl)SO

2

—C

1

-C

4

alkyl, N(C

3

-C

6

alkynyl)SO

2

-phenyl, N(C

3

-C

7

cycloalkyl)SO

2

—C

1

-C

4

alkyl, N(C

3

-C

7

cycloalkyl)SO

2

-phenyl, N(phenyl)SO

2

—C

1

-C

4

alkyl, N(phenyl)SO

2

-phenyt, OSO

2

—C

1

-C

4

alkyl, CONR

028

R

029

, OSO

2

—C

1

-C

4

haloalkyl, OSO

2

-phenyl, C

1

-C

4

alkylthio, C

1

-C

4

haloalkylthio, phenylthio, C

1

-C

4

alkylsulfonyl, C

1

-C

4

haloalkylsu ifonyl, phenylsulfonyl, C

1

-C

4

alkylsulfinyl, C

1

-C

4

haloalkylsulfinyl, phenylsulfinyl, C

1

-C

4

alkylene-phenyl or —NR

031

CO

2

R

030

;

or R

01

is C

3

-C

7

cycloalkyl, C

3

-C

7

cycloalkyl substituted by C

1

-C

4

alkyl, C

1

-C

4

alkoxy, C

1

-C

4

alkylthio, C

1

-C

4

alkylsulfinyl, C

1

-C

4

alkylsulfonyl or phenyl, which for its part may be substituted by halogen, nitro, cyano, C

1

-C

4

alkoxy, C

1

-C

4

haloalkoxy, C

1

-C

4

alkylthio, C

1

-C

4

haloalkylthio, C

1

-C

4

alkyl and C

1

-C

4

haloalkyl; or

R

01

is C

1

-C

4

alkylene-C

3

-C

7

cycloalkyl, phenyl, or phenyl which is substituted by C

1

-C

4

alkyl, C

1

-C

6

haloalkyl, C

1

-C

4

alkoxy, C

1

-C

4

haloalkoxy, C

2

-C

6

alkenyl, C

3

-C

6

alkynyl, C

3

-C

6

alkenyloxy, C

3

-C

6

alkynyloxy, halogen, nitro, cyano, —COOH, COOC

1

-C

4

alkyl, COOphenyl, C

1

-C

4

alkoxy, phenoxy, (C

1

-C

4

alkoxy)-C

1

-C

4

alkyl, (C

1

-C

4

alkylthio)-C

1

-C

4

alkyl, (C

1

-C

4

alkylsulfinyl)-C

1

-C

4

alkyl, (C

1

-C

4

alkylsulfonyl)-C

1

-C

4

alkyl, NHSO

2

—C

1

-C

4

alkyl, NHSO

2

-phenyl, N(C

1

-C

6

alkyl)SO

2

—C

1

-C

4

alkyl, N(C

1

-C

6

alkyl)SO

2

-phenyl, N(C

2

-C

6

alkenyl)SO

2

—C

1

-C

4

alkyl, N(C

2

-C

6

alkenyl)SO

2

-phenyl, N(C

3

-C

6

alkynyl)SO

2

—C

1

-C

4

alkyl, N(C

3

-C

6

alkynyl)SO

2

-phenyl, N(C

3

-C

7

cycloalkyl)SO

2

—C

1

-C

4

alkyl, N(C

3

-C

7

cycloalkyl)SO

2

-phenyl, N(phenyl)SO

2

—C

1

-C

4

alkyl, N(phenyl)SO

2

-phenyl, OSO

2

—C

1

-C

4

alkyl, CONR

045

R

046

, OSO

2

—C

1

-C

4

haloalkyl, OSO

2

-phenyl, C

1

-C

4

alkylthio, C

1

-C

4

haloalkylthio, phenylthio, C

1

-C

4

alkylsulfonyl, C

1

-C

4

haloalkylsulfonyl, phenylsutfonyl, C

1

-C

4

alkylsulfinyl, C

1

-C

4

haloalkylsulfinyl, phenylsulfinyl, or —NR

048

CO

2

R

047

; or

R

01

is C

1

-C

4

alkylene-phenyl, COR

07

or 4-6-membered heterocyclyl;

R

02

, R

038

, R

044

and R

066

independently of one another are hydrogen, C

1

-C

4

alkyl, phenyl, or phenyl which is substituted by C

1

-C

4

alkyl, C

1

-C

6

haloalkyl, C

1

-C

4

alkoxy, C

1

-C

4

haloalkoxy, C

2

-C

6

alkenyl, C

3

-C

6

alkynyl, C

3

-C

6

alkenyloxy, C

3

-C

6

alkynyloxy, halogen, nitro, cyano, —COOH, COOC

1

-C

4

alkyl, COOphenyl, C

1

-C

4

alkoxy, phenoxy, (C

1

-C

4

alkoxy)-C

1

-C

4

alkyl, (C

1

-C

4

alkylthio)-C

1

-C

4

alkyl, (C

1

-C

4

alkylsulfinyl)-C

1

-C

4

alkyl, (C

1

-C

4

alkylsulfonyl)-C

1

-C

4

alkyl, NHSO

2

—C

1

-C

4

alkyl, NHSO

2

-phenyl, N(C

1

-C

6

alkyl)SO

2

—C

1

-C

4

alkyl, N(C

1

-C

6

alkyl)SO

2

-phenyl, N(C

2

-C

6

alkenyl)SO

2

-C

1

-C

4

alkyl, N(C

2

-C

6

alkenyl)SO

2

-phenyl, N(C

3

-C

6

alkynyl)SO

2

—C

1

-C

4

alkyl, N(C

3

-C

6

alkynyl)SO

2

-phenyl, N(C

3

-C

7

cycloalkyl)SO

2

-C

1

-C

4

alkyl, N(C

3

-C cycloalkyl)SO

2

-phenyl, N(phenyl)SO

2

—C

1

-C

4

alkyl, N(phenyl)SO

2

-phenyl, OSO

2

—C

1

-C

4

alkyl, CONR

049

R

050

, OSO

2

—C

1

-C

4

haloalkyl, OSO

2

-phenyl, C

1

-C

4

alkylthio, C

1

-C

4

haloalkylthio, phenylthio, C

1

-C

4

alkylsuffonyl, C

1

-C

4

haloalkylsulfonyl, phenylsulfonyl, C

1

-C

4

alkylsulfinyl, C

1

-C

4

haioalkylsulfinyl, phenylsultinyl, C

1

-C

4

alkylene phenyl or —NR

052

CO

2

R

053

;

R

03

, R

039

and R

067

independently of one another are C

1

-C

4

alkyl, phenyl or phenyl which is substituted by C

1

-C

4

alkyl, C

1

-C

6

haloalkyl, C

1

-C

4

alkoxy, C

1

-C

4

haloalkoxy, C

2

-C

6

alkenyl, C

3

-C

6

alkynyl, C

3

-C

6

alkenyloxy, C

3

-C

6

alkynyloxy, halogen, nitro, cyano, —COOH, COOC

1

-C

4

alkyl, COOphenyl, C

1

-C

4

alkoxy, phenoxy, (C

1

-C

4

alkoxy)-C

1

-C

4

alkyl, (C

1

-C

4

alkylthio)-C

1

-C

4

alkyl, (C

1

-C

4

alkylsulfinyl)-C

1

-C

4

alkyl, (C

1

-C

4

alkylsulfonyl)-C

1

-C

4

alkyl, NHSO

2

—C

1

-C

4

alkyl, NHSO

2

-phenyl, N(C

1

-C

6

alkyl)SO

2

—C

1

-C

4

alkyl, N(C

1

-C

6

alkyl)SO

2

-phenyl, N(C

2

-C

6

alkenyl)SO

2

—C

1

-C

4

alkyl, N(C

2

-C

6

alkenyl)SO

2

-phenyl, N(C

3

-C

6

alkynyl)SO

2

—C

1

-C

4

alkyl, N(C

3

-C

6

alkynyl)SO

2

-phenyl, N(C

3

-C

7

cycloalkyl)SO

2

—C

1

-C

4

alkyl, N(C

3

-C

7

cycloalkyl)SO

2

-phenyl, N(phenyl)SO

2

—C

1

-C

4

alkyl, N(phenyl)SO

2

-phenyl, OSO

2

—C

1

-C

4

alkyl, CONRO

070

R

054

, OSO

2

—C

1

-C

4

haloalkyl, OSO

2

-phenyl, C

1

-C

4

alkylthio, C

1

-C

4

haloalkylthio, phenylthio, C

1

-C

4

alkylsulfonyl, C

1

-C

4

haloalkylsulfonyl, phenylsulfonyl, C

1

-C

4

alkylsulfinyl, C

1

-C

4

haloalkylsulfinyl, phenylsulfinyl, C

1

-C

4

alkylene-phenyl or —NR

056

CO

2

R

055

;

R

04

is C

1

-C

4

alkyl;

R

05

is hydrogen, C

1

-C

4

alkyl, C

2

-C

6

alkenyl, C

3

-C

6

alkynyl, C

3

-C

7

cycloalkyl, phenyl or phenyl which is substituted by C

1

-C

4

alkyl, C

1

-C

6

haloalkyl, C

1

-C

4

alkoxy, C

1

-C

4

haloalkoxy, C

2

-C

6

alkenyl, C

3

-C

6

alkynyl, C

3

-C

6

alkenyloxy, C

3

-C

6

alkynyloxy, halogen, nitro, cyano, —COOH, COOC

1

-C

4

alkyl, COOphenyl, C

1

-C

4

alkoxy, phenoxy, (C

1

-C

4

alkoxy)-C

1

-C

4

alkyl, (C

1

-C

4

alkylthio)-C

1

-C

4

alkyl, (C

1

-C

4

alkylsulfinyl)-C

1

-C

4

alkyl, (C

1

-C

4

alkylsulfonyl)-C

1

-C

4

alkyl, NHSO

2

—C

1

-C

4

alkyl, NHSO

2

-phenyl, N(C

1

-C

6

alkyl)SO

2

—C

1

-C

4

alkyl, N(C

1

-C

6

alkyl)SO

2

-phenyl, N(C

2

-C

6

alkenyl)SO

2

—C

1

-C

4

alkyl, N(C

2

-C

6

alkenyl)SO

2

-phenyl, N(C

3

-C

6

alkynyl)SO

2

H, N(C

3

-C

6

alkynyl)SO

2

—C

1

-C

4

alkyl, N(C

3

-C

6

alkynyl)SO

2

-phenyl, N(C

3

-C

7

cycloalkyl)SO

2

H, N(C

3

-C

7

cycloalkyl)SO

2

—C

1

-C

4

alkyl, N(C

3

-C

7

cycloalkyl)SO

2

-phenyl, N(phenyl)SO

2

—C

1

-C

4

alkyl, N(phenyl)SO

2

-phenyl, OSO

2

-C

1

-C

4

alkyl, CONR

057

R

058

, OSO

2

—C

1

-C

4

haloalkyl, OSO

2

-phenyl, C

1

-C

4

alkylthio, C

1

-C

4

haloalkylthio, phenylthio, C

1

-C

4

alkylsulfonyi, C

1

-C

4

haloalkylsulfonyl, phenylsulfonyl, C

1

-C

4

alkyisulfinyl, C

1

-C

4

haloalkylsulfinyl, phenylsulfinyl, C

1

-C

4

alkylenephenyl or —NR

060

CO

2

R

059

;

R

06

is hydrogen, C

1

-C

4

alkyl, C

2

-C

6

alkenyl, C

3

-C

6

alkynyl, C

3

-C

7

cycloalkyl, phenyl or phenyl which is substituted by C

1

-C

4

aikyl, C

1

-C

6

haloalkyl, C

1

-C

4

alkoxy, C

1

-C

4

haloalkoxy, C

2

-C

6

alkenyl, C

3

-C

6

alkynyl, C

3

-C

6

alkenyloxy, C

3

-C

6

alkynyloxy, halogen, nitro, cyano, —COOH, COOC

1

-C

4

alkyl, COOphenyl, C

1

-C

4

alkoxy, phenoxy, (C

1

-C

4

alkoxy)-C

1

-C

4

alkyl, (C

1

-C

4

alkylthio)-C

1

-C

4

alkyl, (C

1

-C

4

alkylsulfinyl)-C

1

-C

4

alkyl, (C

1

-C

4

alkylsulfonyl)-C

1

-C

4

alkyl, NHSO

2

—C

1

-C

4

alkyl, NHSO

2

-phenyl, N(C

1

-C

6

alkyl)SO

2

—C

1

-C

4

alkyl, N(C

1

-C

6

alkyl)SO

2

-phenyl, N(C

2

-C

6

alkenyl)SO

2

—C

1

-C

4

alkyl, N(C

2

-C

6

alkenyl)SO

2

-phenyl, N(C

3

-C

6

alkynyl)SO

2

—C

1

-C

4

alkyl, N(C

3

-C

6

alkynyl)SO

2

-phenyl, N(C

3

-C

7

cycloalkyl)SO

2

—C

1

-C

4

alkyl, N(C

3

-C

7

cycloaikyl)SO

2

-phenyl, N(phenyl)SO

2

—C

1

-C

4

alkyl, N(phenyl)SO

2

-phenyl, OSO

2

-C

1

-C

4

alkyl, CONR

061

R

062

, OSO

2

—C

1

-C

4

haloalkyl, OSO

2

-phenyl, C

1

-C

4

alkylthio, C

1

-C

4

haloalkylthio, phenylthio, C

1

-C

4

alkylsulfonyl, C

1

-C

4

haloalkylsulfonyl, phenylsulfonyl, C

1

-C

4

alkylsulfinyl, C

1

-C

4

haloalkylsulfinyl, phenylsulfinyl, C

1

-C

4

alkylene-phenyl or —NR

064

CO

2

R

063

;

R

07

is phenyl, substituted phenyl, C

1

-C

4

alkyl, C

1

-C

4

alkoxy or —NR

08

R

09

;

R

08

and R

09

independently of one another are C

1

-C

4

alkyl, phenyl or phenyl which is substituted by halogen, nitro, cyano, C

1

-C

4

alkyl, C

1

-C

4

alkoxy, C

1

-C

4

thioalkyl, —CO

2

R

066

, —COR

067

, C

1

-C

4

alkylsulfonyl, C

1

-C

4

alkylsulfinyl, C

1

-C

4

haloalkyl; or R

08

and R

09

together form a 5-6-membered ring which may be interrupted by oxygen, NR

065

or S,

R

015

, R

031

, R

043

, R

048

, R

052

, R

056

, R

060

and R

064

independently of one another are hydrogen, C

1

-C

4

alkyl, C

2

-C

6

alkenyl, C

3

C

6

alkynyl or C

3

-C

7

cycloalkyl;

R

025

, R

026

, R

027

, R

028

, R

029

, R

030

, R

032

, R

033

, R

034

, R

035

, R

036

, R

037

, R

040

, R

041

, R

042

, R

045

, R

046

, R

047

, R

049

, R

050

, R

053

, R

054

, R

055

, R

057

, R

058

, R

059

, R

061

, R

062

, R

063

, R

065

and R

070

independently of one another are hydrogen, C

1

-C

4

alkyl, C

2

-C

6

alkenyl, C

3

-C

6

alkynyl, C

3

-C

7

cycloalkyl, phenyl, or phenyl which is substituted by halogen, nitro, cyano, C

1

-C

4

alkoxy, C

1

-C

4

haloalkoxy, C

1

-C

4

alkylthio, C

1

-C

4

haloalkylthio, C

1

-C

4

alkyl or C

1

-C

4

haloalkyl; and

R

36

is C

1

-C

4

alkyl, C

1

-C

4

haloalkyl, C

3

-C

6

alkenyl, C

3

-C

6

haloalkenyl, C

3

-C

6

alkynyl, C

3

-C

6

haloalkynyl, C

3

-C

6

cycloalkyl or C

3

-C

6

cycloaikyl which is substituted by halogen, C

1

-C

4

alkyl, C

1

-C

4

haloalkyl, C

3

-C

6

alkenyl, C

3

-C

6

haloalkenyl, C

3

-C

6

alkynyl, C

3

-C

6

haloalkynyl, C

1

-C

4

alkoxycarbonyl, C

1

-C

4

alkylthio, C

1

-C

4

alkylsulfinyl, C

1

-C

4

alkylsulfonyl, C

1

-C

4

haloalkylthio, C

1

-C

4

haloalkylsulfinyl, C

1

-C

4

haloalkylsulfonyl, C

1

-C

4

alkylcarbonyl, di-C

1

-C

4

alkylamino, C

1

-C

4

alkoxy, C

1

-C

4

haloalkoxy, C

1

-C

4

alkyl-S(O)

2

O, C

1

-C

4

haloalkyl-S(O)

2

O or phenyl which for its part may be substituted by halogen, C

1

-C

4

alkyl, C

1

-C

4

haloalkyl, C

3

-C

6

alkenyl, C

3

-C

6

alkynyl, cyano, nitro or COOH; and agronomically acceptable salts M

+

and all stereoisomers and tautomers of the compounds of the formula I.

The compounds of the formula I can be present in different isomeric forms which can be isolated in pure form. The invention therefore also embraces all stereoisomeric forms of the compound of the formula I. Examples of these isomeric forms are the formulae Ix, Ixx, Ixxx and Ixxxx below, in which Q is the group Q

2

.

The alkyl groups occurring in the definitions of the substituents can be straight-chain or branched and are, for example, methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, iso-butyl, tert-butyl, pentyl, hexyl, heptyl and octyl and their branched isomers. Alkoxy, alkenyl and alkynyl radicals are derived from the alkyl radicals mentioned. The alkenyl and alkynyl groups can be mono- or polyunsaturated.

Halogen is generally fluorine, chlorine, bromine or iodine. This also applies, correspondingly, to halogen in combination with other meanings, such as haloalkyl or halophenyl.

Haloalkyl groups preferably have a chain length of from 1 to 8 carbon atoms. Haloalkyl is, for example, fluoromethyl, difluoromethyl, trifluoromethyl, chloromethyl, dichloromethyl, trichloromethyl, 2,2,2-trifluoroethyl, 2-fluoroethyl, 2-chloroethyl, pentafluoroethyl, 1,1-difluoro-2,2,2-trichloroethyl, 2,2,3,3-tetrafluoroethyl and 2,2,2-trichloroethyl; preferably trichloromethyl, difluorochloromethyl, difluoromethyl, trifluoromethyl and dichlorofluoromethyl.

Suitable haloalkenyl groups are alkenyl groups which are mono- or polysubstituted by halogen, halogen being fluorine, chlorine, bromine and iodine and in particular fluorine and chlorine, for example 2,2-difluoro-1-methylvinyl, 3-fluoropropenyl, 3-chloropropenyl, 3-bromopropenyl, 2,3,3-trifluoropropenyl, 2,3,3-trichloropropenyl and 4,4,4-trifluorobut-2-en-1-yl. Among the C

3

-C

20

alkenyl groups which are mono-, di- or trisubs btuted by halogen, preference is given to those having a chain length of from 3 to 5 carbon atoms.

Suitable haloalkynyl groups are, for example, aikynyl groups which are mono- or polysubstituted by halogen, halogen being bromine, iodine and in particular fluorine and chlorine, for example 3-fluoropropynyl, 3-chloropropynyl, 3-bromopropynyl, 3,3,3-trifluoropropynyl and 4,4,4-trifluorobut-2-yn-1-yl. Among the alkynyl groups which are mono- or polysubstituted by halogen, preference is given to those having a chain length of from 3 to 5 carbon atoms.

Alkoxy groups preferably have a chain length of from 1 to 6 carbon atoms. Alkoxy is, for example, methoxy, ethoxy, propoxy, i-propoxy, n-butoxy, isobutoxy, sec-butoxy and tert-butoxy and also the isomeric pentyloxy and hexyloxy radicals; preferably methoxy and ethoxy. Alkylcarbonyl is preferably acetyl or propionyl. Alkoxycarbonyl is, for example, methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, isopropoxycarbonyt, n-butoxycarbonyl, isobutoxycarbonyl, sec-butoxycarbonyl or tert-butoxycarbonyl; preferably methoxycarbonyl or ethoxycarbonyl. Haloalkoxy groups preferably have a chain length of from 1 to 8 carbon atoms. Haloalkoxy is, for example, fluoromethoxy, difluoromethoxy, trifluoromethoxy, 2,2,2-trifluoroethoxy, 1,1,2,2-tetrafluoroethoxy, 24luoroethoxy, 2-chloroethoxy, 2,2-difluoroethoxy and 2,2,2-trichloroethoxy; preferably difluoromethoxy, 2-chloroethoxy and trifluoromethoxy. Alkylthio groups preferably have a chain length of from 1 to 8 carbon atoms. Alkylthio is, for example, methylthio, ethylthio, propylthio, isopropylthio, n-butylthio, isobutylthio, sec-butylthio or tert-butylthio, preferably methylthio and ethylthio. Alkylsuffinyl is, for example, methylsulfinyl, ethylsulfinyl, propyisulfinyl, isopropylsulfinyl, n-butylsulfinyl, isobutylsulfiny l, sec-butylsulfinyl, tert-butylsulfinyl; preferably methylsulfinyl and ethylsulfinyl. Alkylsulfonyl is, for example, methylsulfonyl, ethylsulfonyl, propylsulfonyl, isopropylsulfonyl, n-butylsulfonyl, isobutylsulfonyl, sec-butylsulfonyl or tert-butylsulfonyl; preferably methylsulfonyl or ethylsulfonyl. Alkoxyalkoxy groups preferably have a chain length of from 1 to 8 carbon atoms. Examples of alkoxyalkoxy groups are: methoxymethoxy, methoxyethoxy, methoxypropoxy, ethoxymethoxy, ethoxyethoxy, propoxymethoxy or butoxybutoxy. Alkylamino is, for example, methylamino, ethylamino, n-propylamino, isopropylamino or the isomeric butylamines. Dialkylamino is, for example, dimethylamino, methylethylamino, diethylamino, n-propylmethylamino, dibutylamino and diisopropylamino. Preference is given to alkylamino groups having a chain length of from 1 to 4 carbon atoms. Alkoxyalkyl groups have a chain length of preferably from 1 to 6 carbon atoms. Alkoxyalkyl is, for example, methoxymethyl, methoxyethyl, ethoxymethyl, ethoxyethyl, n-propoxymethyl, n-propoxyethyl, isopropoxymethyl or isopropoxyethyl. Alkylthioalkyl groups preferably have from 1 to 8 carbon atoms. Alkylthioalkyl is, for example, methylthiomethyl, methylthioethyl, ethylthiomethyl, ethylthioethyl, n-propylthiomethyl, n-propylthioethyl, isopropylthiomethyl, iso-propylthioethyl, butylthiomethyl, butylthioethyl or butylthiobutyl. The cycloalkyl groups preferably have from 3 to 8 ring carbon atoms, for example cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and cyclooctyl. Phenyl, also as part of a substituent as phenoxy, benzyl, benzyloxy, benzoyl, phenylthio, phenylalkyl, phenoxyalkyl, may be substituted. In this case, the substituents can be in ortho, meta and/or para position. The preferred substituent positions are the ortho and para positions to the ring attachment point. Heterocyclyl is to be understood as meaning ring systems which, in addition to carbon atoms, contain at least one heteroatom, such as nitrogen, oxygen and/or sulfur. They can be saturated or unsaturated. In the context of the present invention, heterocyclyl ring systems may also be substituted. Suitable substituents are, for example, C

1

-C

4

alkyl, C

1

-C

4

haloalkyl, C

1

-C

4

alkoxy, cyano, nitro, C

1

-C

4

alkylsulfonyl, C

1

-C

4

alkylsulfinyl, C

1

-C

4

alkylthio or C

3

-C

6

cycloalkyl.

Heterocyclyl may be, for example, furyl, thiophenyl, pyrrolidyl, piperidinyl, morpholinyl, pyridyl, imidazolyl, tetrahydrofuryl, tetrahydropyranyl, dihydrofuryl, dihydropyranyl, isoxazolyl, oxazolyl, isothiazolyl, 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, thiazolyl, pyrazolyl, 1,2,4-triazolyl, 1,2,3-triazolyl, tetrazolyl, pyrimidyl, pyrazinyl, sym. or unsym. triazinyl, piperazinyl, oxazolinyl (for example:

oxazolidinyl, imidazolinyl, imidazolidinyl, dioxanyl, oxetanyl, in particular 2-oxetanyl, or phthalimidyl.

The invention also embraces the salts M

+

which can be formed by the compounds of the formula 1, in particular the compounds of the formula I in which R

20

, R

23

, R

26

and R

30

are hydroxyl, preferably with amines, alkali metal and alkaline earth metal bases or quaternary ammonium bases. Among the alkali metal and alkaline earth metal bases, the hydroxides of lithium, sodium, potassium, magnesium or calcium, in particular those of sodium or potassium, may be especially emphasized as salt formers. Examples of amines suitable for ammonium salt formation are both ammonia and primary, secondary and tertiary C

1

-C

18

alkylamines, C

1

-C

4

hydroxyalkylamines and C

2

-C

4

alkoxyalkylamines, for example methylamine, ethylamine, n-propylamine, isopropylamine, the four isomeric butylamines, n-amylamine, isoamylamine, hexylamine, heptylamine, octylamine, nonylamine, decylamine, pentadecylamine, hexadecylamine, heptadecylamine, octadecylamine, methylethylamine, methylisopropylamine, methylhexylamine, methylnonylamine, methylpentadecylamine, methyloctadecylamine, ethylbutylamine, ethylheptylamine, ethyloctylamine, hexylheptylamine, hexyloctylamine, dimethylamine, diethylamine, di-n-propylamine, diisopropylamine, di-n-butylamine, di-n-amylamine, diisoamylamine, dihexylamine, diheptylamine, dioctylamine, ethanolamine, n-propanolamine, isopropanolamine, N,N-diethanolamine, N-ethylpropanolamine, N-butylethanolamine, al iylamine, n-butenyl-2-amine, n-pentenyl-2-amine, 2,3dimethylbutenyl-2-amine, dibutenyl-2-amine, n-hexenyl-2-amine, propylenediamine, trimethylamine, triethylamine, tri-n-propylamine, triisopropylamine, tri-n-butylamine, triisobutylamine, tri-sec-butylamine, tri-n-amylamine, methoxyethylamine and ethoxyethylamine; heterocyclic amiines, for example pyridine, quinoline, isoquinoline, morpholine, piperidine, pyrrolidine, indoline, quinuclidine and azepine: primary arylamines, for example anilines, methoxyanilines, ethoxyanilines, o,m,p-toluidines, phenylenediamines, naphthylamines and o,m,p-chloroanilines; but in particular triethylamine, isopropylamine and diisopropylamine. Quatemary ammonium bases which are suitable for salt formation are, for example, [N(R

a01

R

b01

R

c01

R

d01

)]

+

OH

−

, where R

a01

, R

b01

, R

c01

and R

d01

independently of one anotheer are C

1

-C

4

alkyl. Further suitable tetraalkylammonium bases with other anions can be obtained, for example, by anion exchange reactions.

Preferred compounds of the formula I correspond to the formula Ib

in which

each R independently is C

1

-C

6

alkyl, C

1

-C

6

alkoxy, C

1

-C

6

haloalkoxy, C

1

-C

6

alkylthio, C

1

-C

6

-alkylsulfinyl, C

1

-C

6

alkylsulfonyl, C

1

-C

6

haloalkyl, C

1

-C

6

haloalkylthio, C

1

-C

6

haloalkylsu ffinyl, C

1

-C

6

haloalkylsulfonyl, C

1

-C

6

alkoxycarbonyl, C

1

-C

6

alkylcarbonyl, C

1

-C

6

alkylamino, di-C

1

-C

6

-alkylamino, C

1

-C

6

alkylaminosu ffonyl, di-C

1

-C

6

alkylaminosulfonyl, —N(R

1

)—S—R

2

, —N(R

3

)—SO—R

4

, —N(R

5

)—SO

2

—R

6

, nitro, cyano, halogen, hydroxyl, amino, or a five- to ten-membered monocyclic or fused bicyclic ring system which may be aromatic or partially saturated and may contain 1 to 4 heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur, where the ring system is either attached directly to the pyridine ring or attached via a C

1

-C

4

alkylene group to the pyridine ring, and each ring system may not contain more than 2 oxygen atoms and not more than two sulfur atoms, and the ring system for its part may be mono-, di- or trisubstituted by C

1

-C

6

alkyl, C

1

-C

6

haloalkyl, C

3

-C

6

alkenyl, C

3

-C

6

haloalkenyl, C

3

-C

6

alkynyl, C

3

-C

6

haloalkynyl, C

1

-C

6

alkoxy, C

1

-C

6

haloalkoxy, C

3

-C

6

alkenyloxy, C

3

-C

6

alkynyloxy, mercapto, C

1

-C

6

alkylthio, C

1

-C

6

haloalkylthio, C

3

-C

6

alkenylthio, C

3

-C

6

haloalkenylthio, C

3

-C

6

alkynylthio, C

2

-C

5

alkoxyalkylthio, C

3

-C

6

acetylalkylthio, C

3

-C

6

alkoxycarbonylalkylthio, C

2

-C

4

-cyanoalkylthio, C

1

-C

6

alkylsulfinyl, C

1

-C

6

haloalkylsulfinyl, C

1

-C

6

alkylsulfonyl, C

1

-C

6

-haloalkylsulfonyl, aminosulfonyl, C

1

-C

2

alkylaminosulfonyl, C

2

-C

4

dialkylaminosulfonyl, C

1

-C

3

-alkylene-R

7

, NR

8

R

9

, halogen, cyano, nitro, phenyl and benzylthio where phenyl and benzylthio for their part may be substituted on the phenyl ring by C

1

-C

3

alkyl, C

1

-C

3

haloalkyl, C

1

-C

3

alkoxy, C

1

-C

3

haloalkoxy, halogen, cyano or nitro, and where substituents on the nitrogen in the heterocyclic ring are different from halogen;

Q is the group Q

1

in which

R

20

is hydroxyl, C

1

-C

4

alkoxy, C

1

-C

4

alkylcarbonyloxy, C

1

-C

4

alkoxycarbonyloxy, R

21

R

22

N—C(O)O, phenylthio, C

1

-C

4

alky lthio, C

1

-C

4

alkyl-S(O)

2

O, (C

1

-C

4

alkoxy)

2

P(O)O, C

1

-C

4

alkyl(C

1

-C

4

alkoxy)P(O)O, H(C

1

-C

4

alkoxy)P(O)O or benzoyloxy; and

R

21

, and R

22

independently of one another are hydrogen or C

1

-C

4

alkyl; or the group Q

2a

in which R

23

is hydroxyl, C

1

-C

4

alkoxy, C

1

-C

4

alkylcarbonyloxy, C

1

-C

4

alkoxycarbonyloxy, R

24

R

25

N—C(O)O, phenylthio, C

1

-C

4

alkylthio, C

1

-C

4

alkyl-S(O)

2

O, (C

1

-C

4

alkoxy)

2

P(O)O, C

1

-C

4

-alkyl(C

1

-C

4

alkoxy)P(O)O, H(C

1

-C

4

alkoxy)P(O)O or benzoyloxy; and

R

24

and R

25

independently of one another are hydrogen or C

1

-C

4

alkyl; and

Y is oxygen, sulfur, a chemical bond or a C

1

-C

4

alkylene bridge;

or the group Q

3

in which R

26

is hydroxyl, C

1

-C

4

alkoxy, C

1

-C

4

alkylcarbonyloxy, C

1

-C

4

alkoxycarbonyloxy, R

27

R

28

N-C(O)O, phenylthio, C

1

-C

4

alkylthio, C

1

-C

4

alkyl-S(O)

2

O, (C

1

-C

4

alkoxy)

2

P(O)O, C

1

-C

4

-alkyl(C

1

-C

4

alkoxy)P(O)O, H(C

1

-C

4

alkoxy)P(O)O or benzoyloxy; and

R

27

and R

28

independently of one another are hydrogen or C

1

-C

4

alkyl and

R

29

is hydrogen, C

1

-C

6

alkyl, C

1

-C

4

alkylcarbonyl, C

1

-C

4

alkoxycarbonyl, (C

1

-C

4

alkyl)NHCO or (C

1

-C

4

alkyl)

2

NCO; or the group Q

4

in which R

30

is hydroxyl, C

1

-C

4

alkoxy, C

1

-C

4

alkylcarbonyloxy, C

1

-C

4

alkoxycarbonyloxy, R

31

R

32

N—C(O)O, phenylthio, C

1

-C

4

alkylthio, C

1

-C

4

alkyl-S(O)

2

O, (C

1

-C

4

alkoxy)

2

P(O)O, C

1

-C

4

-alkyl(C

1

-C

4

alkoxy)P(O)O, H(C

1

-C

4

alkoxy)P(O)O or benzoyloxy; and

R

31

and R

32

independently of one another are hydrogen or C

1

-C

4

alkyl;

R

33

and R

34

independently of one another are hydrogen, C

1

-C

4

alkyl, C

2

-C

6

alkenyl, C2-C

6

alkynyl, C

1

-C

4

-alkoxycarbonyl, C

1

-C

6

alkylthio, C

1

-C

6

alkylsulfinyl, C

1

-C

6

alkylsulfonyl, C

1

-C

4

alkyl-NHS(O)

2

, C

1

-C

4

haloalkyl, —NH—C

1

-C

4

alkyl, —N(C

1

-C

4

alkyl)

2

, C

1

-C

6

alkoxy, or phenyl which for its part may be substituted by C

1

-C

4

alkyl, C

1

-C

4

haloalkyl, C

1

-C

4

alkoxy, C

1

-C

4

haloalkoxy, C

1

-C

4

alkylcarbonyl, C

1

-C

4

alkoxycarbonyl, amino, C

1

-C

4

alkylamino, di-C

1

-C

4

alkylamino, C

1

-C

6

alkylthio, C

1

-C

6

-alkylsulfinyl, C

1

-C

6

alkylsulfonyl, C

1

-C

4

alkyl-S(O)

2

O, C

1

-C

4

haloalkylthio, C

1

-C

4

haloalkylsulfinyl, C

1

-C

4

haloalkylsulfonyl, C

1

-C

4

haloalkyl-S(O)

2

O, C

1

-C

4

alkyl-S(O)

2

NH, C

1

-C

4

alkyl-S(O)

2

N(C

1

-C

4

-alkyl), halogen, nitro, COOH or cyano; or R

33

and R

34

together form a C

2

-C

6

alkylene bridge; and

R

35

is hydrogen, C

1

-C

4

alkyl, C

1

-C

4

alkoxycarbonyl or phenyl which for its part may be substituted by C

1

-C

4

alkyl, C

1

-C

4

haloalkyl, C

1

-C

4

alkoxy, C

1

-C

4

haloalkoxy, C

1

-C

4

alkylcarbonyl, C

1

-C

4

alkoxycarbonyl, amino, C

1

-C

4

alkylamino, di-C

1

-C

4

alkylamino, C

1

-C

4

alkylthio, C

1

-C

4

-alkylsulfinyl, C

1

-C

4

alkylsulfonyl, C

1

-C

4

alkyl-S(O)

2

O, C

0

-C

4

haloalkylthio, C

1

-C

4

haloalkylsulfinyl, C

1

-C

4

haloalkylsulfonyl, C

1

-C

4

haloalkyl-S(O)

2

O, C

1

-C

4

alkyl-S(O)

2

NH, C

1

-C

4

alkyl-S(O)

2

N(C

1

-C

4

-alkyl), halogen, nitro, COOH or cyano; or the group Q

5

, and also agronomically acceptable salts of these compounds, the other substituents being defined as under formula I in claim 1. Among the compounds of the formula lb, preference is furthermore given to those in which the group

—C(O)—Q is located in the 3 position on the pyridine ring, or in which Q is Q

2

, R

23

being, in particular, hydroxyl, Y being a methylene bridge and m being the number 2. Preference is further given to compounds of the formula lb in which R is C

1

-C

6

alkyl or C

1

-C

6

haloalkyl.

Preferred compounds of the formula I are characterized in that the group —C(O)Q is in the ortho position to a group R. Preference is furthermore given to compounds of the formula I in which a group R is C

1

-C

6

haloalkyl and in the ortho position to the pyridyl nitrogen. Of particular interest are furthermore compounds of the formula I in which the group —C(O)Q is in the 3 position to the pyridyl nitrogen. In the formula 1, p is preferably the number 0. Also to be emphasized are compounds of the formula I in which m is 2 and R is C

1

-C

3

alkyl, C

1

-C

3

-haloalkyl, C

1

-C

2

alkoxymethyl, C

1

-C

2

alkythiomethyl, hydroxymethyl, C

1

-C

6

alky lcarbonyloxymethyl, benzoyloxymethyl, C

1

-C

4

alkoxycarbonyloxymethyl, chlorine, cyano, C

1

-C

3

alkoxy, C

1

-C

3

haloalkoxy, allyloxy, propargyloxy, C

1

-C

3

alkylthio, C

1

-C

3

alkylsulfinyl, C

1

-C

3

alkylsulfonyl, C

1

-C

3

alkylsulfonyloxy, C

1

-C

2

alkylsulfinylmethyl or C

1

-C

2

alkylsulfonylmethyl. A further group of preferred compounds of the formula I is formed by those compounds in which at least one group R is trifluoromethyl, difluorochloromethyl, pentafluoroethyl or heptafluoro-n-propyl.

Particularly noteworthy compounds of the formula I are those in which Q is a group Q

1

and R

16

, R

18

and R

19

are C

1

-C

3

alkyl and R

17

is hydrogen, or Q is a group Q

2

and Y is —CH

2

—, —CH

2

CH

2

— or oxygen, A is —CH

2

— and R

240

, R

241

, R

242

and R

243

are Mch hydrogen, or Q is a group Q

3

and R

29

is C

1

-C

4

alkylcarbonyl, C

1

-C

4

alkoxycarbonyl or C

1

-C

4

alkylaminocarbonyl or di(C

1

-C

2

-alkyl)aminocarbonyl, or Q is a group Q

4

in which R

33

, R

34

and R

35

are C

1

-C

3

alkyl. In these noteworthy compounds of the formula I, R

20

, R

23

, R

26

and R

30

independently of one another are halogen, thiocyanato, C

1

-C

12

alkoxy, C

1

-C

4

alkoxycarbonyl-C

1

-C

2

alkoxy, C

1

-C

12

-alkylthio, alkylthio, C

1

-C

12

alkylsulfinyl, C

1

-C

12

alkylsulfonyl, C

1

-C

12

haloalkylthio, C

1

-C

12

haloalkylsulfinyl, C

1

-C

12

haloalkylsulfonyl, C

1

-C

12

alkenylthio, C

2

-C

12

alkenylsulfinyl, C

2

-C

12

alkenylsulfonyl, C

2

-C

12

-haloalkenylthio, C

2

-C

12

haloalkenylsulfinyl, C

2

-C

12

haloalkenylsulfonyl, C

2

-C

12

alkynylthio, C

2

-C

12

alkynylsulfinyl, C

2

-C

12

alkynylsulfonyl, C

1

-C

4

alkoxycarbonyl-C

1

-C

2

-alkylthio, C

1

-C

4

-alkoxycarbonyl-C

1

-C

2

alkylsulfinyl, C

1

-C

4

alkoxycarbonyl-C

1

-C

2

alkylsulfonyl, C

1

-C

4

alkyl-S(O)

2

NH, C

1

-C

4

haloalkyl-S(O)

2

NH, C

1

-C

4

alkyl-S(O)

2

O, C

1

-C

18

alkylcarbonyloxy, C

2

-C

18

-alkenylcarbonyloxy, C

3

-C

6

cycloalkylcarbonyloxy, C

1

-C

12

alkoxycarbonyloxy, C

1

-C

12

-alkylthiocarbonyloxy, C

1

-C

12

alkylthiocarbamoyl, C

1

-C

6

alkyl-NH(CS)N(C

1

-C

6

alkyl)—NH—, di-C

1

-C

6

alkyl-N(CS)N(C

1

-C

6

alkyl)—NH—, benzyloxy, benzylthio, benzylsulfinyl, benzylsulfonyl, phenoxy, phenylthio, phenylsulfinyl, phenylsulfonyl, phenylsulfonyloxy or benzoyloxy, where the phenyl groups for their part may in each case be substituted by C

1

-C

4

alkyl, C

1

-C

4

-haloalkyl, C

1

-C

4

alkoxy, C

1

-C

4

haloalkoxy, C

1

-C

4

alkylcarbonyl, C

1

-C

4

alkoxycarbonyl, C

1

-C

4

-alkylamino, di-C

1

-C

4

alkylamino, C

1

-C

4

alkylthio, C

1

-C

4

alkylsulfinyl, C

1

-C

4

alkylsuonyl, C

1

-C

4

-alkyl-S(O)

2

O, C

1

-C

4

haloalkylthio, C

1

-C

4

haloalkylsulfinyl, C

1

-C

4

haloalky lsulfonyl, C

1

-C

4

-haloalkyl-S(O)

2

O, C

1

-C

4

alkyl-S(O)

2

NH, C

1

-C

4

alkyl-S(O)

2

N(C

1

-C

4

alkyl), halogen, nitro or cyano, or R

20

, R

23

, R

26

and R

30

independently of one another are thienylcarbonyloxy or furylcarbonyloxy which for their part may be substituted by methyl or halogen, or are pyridylcarbonyloxy which for its part may be substituted as stated in claim 1, or R

20

is R

37

R

37

N, R

71

R

72

NNH—, R

21

R

22

NC(O)O— or R

73

R

74

NC(O)NH—; or R

23

is R

44

R

45

N, R

75

R

76

NNH—, R

46

R

47

NC(O)O— or R

77

R

78

NC(O)NH—; or R

26

is R

53

R

54

N, R

79

R

80

NNH—, R

55

R

56

NC(O)O— or R

81

R

82

NC(O)NH—; or R

30

is R

62

R

63

N, R

83

R

84

NNH—, R

64

R

65

NC(O)O— or R

85

R

86

NC(O)NH—. Very particularly preferably, R

20

, R

23

, R

26

or R

30

are hydroxyl or O

−

M

+

.

A further preferred group is formed by those compounds of the formula I in which Q is a group Q

5

, R

36

is C

1

-C

4

alkyl, C

1

-C

4

haloalkyl or cyclopropyl and R

01

is C

1

-C

6

alkyl, C

1

-C

4

-alkoxycarbonylmethyl, C

3

-C

8

alkenyl, is benzyl or phenyl substituted by methyl, halogen, trifluoromethyl, methoxy, and at least one group R is trifluoromethyl, difluorochloromethyl, pentafluoroethyl or heptafluoro-n-propyl located in the ortho position to the pyridyl nitrogen.

The process according to the invention for preparing compounds of the formula I

in which R and m are as defined under formula 1; p is 0 and Q is the group

is carried out analogous ly to known processes (for example those described in WO 97/46530 and EP-A-0 353 187) and comprises

a) reacting a compound of the formula II

in which R and m are as defined under formula I and X is a leaving group, for example halogen, in an inert organic solvent in the presence of a base with compounds of the formula III, IV,V or VI

in which R

16

, R

17

, R

18

, R

19

,R

29

, R

33

, R

34

, R

35

, R

240

, R

243

, R

242

, R

241

, A and Y are as defined under formula I to give the compounds of the formula VII, VIII, IX or X

and then isomerizing these compounds, for example in the presence of a base and a catalytic amount of dimethylaminopyridine (DMAP) or a source of cyanide; or

b) reacting a compound of the formula XI

in which R and m are as defined under formula I with compounds of the formula III, IV, V or VI

in which R

16

, R

17

, R

18

, R

19

, R

29

, R

33

, R

34

, R

35

, R

240

, R

243

, R

242

, R

241

, A and Y are as defined under formula I in an inert organic solvent in the presence of a base and a coupling agent to give a compound of the formula VII, VIII, IX or X

and then isomerizing these compounds, for example as described under route a).

Compounds of the formula I in which R

20

, R

23

, R

26

and R

30

are different from hydroxyl or halogen can be prepared by converesion methods which are generally known from the literature, for example acyclations or carbamoylations with appropriate acyl chlorides, from compounds in which R

20

, R

23

, R

26

or R

30

is hydroxyl in the presence of a suitable base, or they can be prepared by nucleophilic substitution reactions on chlorides of the formula I in which R

20

, R

23

, R

26

or R

30

is halogen, which are likewise obtainable by known processes by reaction with a chlorinating agent, such as phosgene, thionyl chloride or oxalyl chloride. Here, for example, suitably substituted amines, or hydroxylamines directly, or alkylsulfonamides, mercaptans, thiophenols, phenols, Ar

1

—NH

2

or Ar

1

—SH, are employed in the presence of a base, for example 5-ethyl-2-methylpyridine, diisopropylethylamine, triethylamine, sodium bicarbonate, sodium acetate or potassium carbonate.

Compounds of the formula I in which R

20

, R

23

, R

26

or R

30

comprise thio groups can be oxidized analogously to known standard processes, for example using peracids, for example meta-chloroperbenzoic acid (m-CPBA) or peracetic acid, to give the corresponding sulfones and sulfoxides of the formula I. Here, the degree of oxidation at the sulfur atom (SO— or SO

2

—) can be controlled by the amount of oxidizing agent.

The process according to the invention for preparing compounds of the formula I in which R and m are as defined under formula I and Q is a group

in which Z is sulfur, q is 0 and R

36

and R

01

are as defined under formula I is carried out analogously to known processes (for example those described in WO 97/43270) and comprises converting a compound of the formula XII

in which R

36

, R and m are as defined under formula I in the presence of a base, carbon disulfide and an alkylating agent of the formula XIII

R

01

—X

1

(XIII),

in which R

01

is as defined under formula I and X

1

is a leaving group, for example halogen or sulfonate, into the compound of the formula XIV

in which Z is sulfur and R, R

01

, R

36

and m are as defined above and then cyclizing this compound using hydroxylamine hydrochloride, in the presence or absence of a solvent, in the presence of a base to give the compounds of the formulae

in which Z is sulfur and R, R

36

, R

01

and m are as defined above, and then oxidizing these compounds with an oxidizing agent, for example meta-chloroperbenzoic acid (m-CPBA). The isomers of the formulae le and If can be separated using column chromatography and a suitable mobile phase and then purified.

The preparation of the compounds of the formula I in which p is 0 is illustrated in more detail in the reaction schemes 1 and 2 below.

According to this reaction scheme, the compounds of the formula I with the group Q

1

in which R

20

is hydroxyl, the compounds of the formula I with the group Q

2

in which R

23

is hydroxyl, the compounds of the formula I with the group Q

3

in which R

26

is hydroxyl and the compounds of the formula I with the group Q

4

in which R

30

is hydroxyl can preferably be prepared.

For preparing the compounds of the formula I in which Q is the groups Q

1

to Q

4

and R

20

, R

23

,R

26

and R

30

are hydroxyl, in accordance with reaction scheme 1, route a), the carboxylic acid derivatives of the formula II in which X is a leaving group, for example halogen, for example iodine, bromine and in particular chlorine, N-oxyphthali r nide or N,O— dimethylhydroxylamino or part of an activated ester, for example

(formed from dicyclohexylcarbodiimide (DCC) and the corresponding carboxylic acid) or

(formed from N-ethyl-N′-(3-dimethyiaminopropyl)carbodiimide (EDC) and the corresponding carboxylic acid) are employed. These compounds are reacted in an inert organic solvent, for example a halogenated hydrocarbon, for example dichloromethane, a nitrile, for example acetonitrile, or an aromatic hydrocarbon, for example toluene, and in the presence of a base, for example an alkylamine, for example triethylamine, an aromatic amine, for example pyridine or 4-dimethyiaminopyridine (DMAP), with the dione derivatives of the formula III, IV, V or VI to give the isomeric enol ethers of the formulae VII, VIII, IX and X. This esterification is carried out at temperatures of from 0° C. to 110° C.

The isomerization of the ester derivatives of the formulae VII, VIII, IX and X to the dione derivatives of the formula I (in which R

20

, R

23

, R

26

and R

30

are hydroxyl) can be carried out, for example, analogously to EP 369 803 in the presence of a base, for example an alkylamine, for example triethylamine, a carbonate, for example potassium carbonate, and a catalytic amount of DMAP or a cyanide source, for example acetone cyanohydrin or potassium cyanide.

According to reaction scheme 1, route b), the desired diones of the formula I (in which R

20

, R

23

, R

26

and R

30

are hydroxyl) can be obtained, for example, in analogy to Chem. Lett. 1975, 1045 by esterifying the carboxylic acids of the formula Xl with the dione derivatives of the formula III, IV, V or VI in an inert solvent, for example a halogenated hydrocarbon, for example dichloromethane, a nitrile, for example acetonitrile, or an aromatic hydrocarbon, for example toluene, in the presence of a base, for example an alkylamine, for example triethylamine, and a coupling agent, for example 2-chloro-1-methylpyridinium iodide. Depending on the solvent used, this esterification is carried out at temperatures of from 0° C. to 110° C., affording initially, as described under route a), the isomeric ester of the formula I which can be isomerized as described under route a), for example in the presence of a base and a catalytic amount of DMAP, or a cyanide source, to give the desired dione derivative of the formula I (R

20

, R

23

, R

26

and R

30

are hydroxyl).

The preparation of the compounds of the formula I in which Q is the group Q

5

can be carried out in accordance with reaction scheme 2 by reacting the β-diketone derivative of the formula XII, for example in analogy to Synthesis 1991, 301; ibid. 1988, 793; or Tetrahedron 32, 3055 (1976) with carbon disulfide in the presence of a base, for example a carbonate, for example potassium carbonate, a metal hydride, for example sodium hydride, or potassium fluoride on aluminium, and an alkylating agent of the formula XIII in which X

1

is a leaving group, for example halogen, for example iodine, bromine and in particular chlorine,

This reaction is preferably carried out in the presence of a solvent, for example an amide, for example N,N-dimethylformamide (DMF), a sulfoxide, for example dimethylsulfoxide (DMSO), or a nit rle, for example acetonitrile. The ketene thioacetal of the formula XIV which is formed is cyclized with the aid of hydroxylamine hydrochloride in the presence of a base, for example sodium acetate, in a solvent, for example an alcohol, for example ethanol, or an ether, for example tetrahydrofuran, to give the compound of the formula le in which Z is sulfur. This cyclization reaction is carried out at temperatures of from 0° C. to 100° C. If appropriate, compounds of the formulae le and If (Z is sulfur) can be oxidized analogously to known standard processes, for example with peracids, for example meta-chloroperbenzoic acid (m-CPBA) or peracetic acid, to give the corresponding sulfones and sulfoxides of the formulae Ie and If (Z═SO— or SO

2

—). Here, the degree of oxidation at the sulfur atom (Z═SO— or SO

2—

) can be controlled by the amount of oxidizing agent.

Oxidations to the compounds of the formulae le and If (Z is SO— or SO

2—

) are carried out as described, for example, in H.O. House, “Modern Synthetic Reactions” W. A. Benjamin, Inc., Menlo Park, Calif., 1972, pages 334-335 and 353-354.

The activated carboxylic acid derivatives of the formula II in reaction scheme 1 (route a) in which X is a leaving group, for example halogen, for example bromine, iodine or in particular chlorine, can be prepared by known standard processes, as described, for example, in C. Ferri “Reaktionen der organischen Synthese” [Reactions of Organic Synthesis], Georg Thieme Verlag, Stuttgart, 1978, page 461 ff. This is shown in reaction scheme 3 below.

According to reaction scheme 3, the compounds of the formula II (X=leaving group) or II (X=halogen) are prepared, for example, by employing a halogenating agent, for example a thionyl halide, for example thionyl chloride or thionyl bromide; a phosphorus halide or phosphorus oxyhalide, for example phosphorus pentachloride or phosphorus oxychloride or phosphorus pentabromide or phosphoryl bromide; or an oxalyl halide, for example oxalyl chloride, or by employing a reagent for the formation of activated esters, for example N,N′-dicyclohexylcarbodiimide (DCC) or N-ethyl-N′-(3-dimethylaminopropyli)carbodiimide (EDC) of the formula X. For the compound of the formula X used as halogenating agents, X is a leaving group, for example halogen, for example fluorine, bromine or iodine and in particular chlorine, and W

1

is, for example, PCI

2

, SOCI, SOBr or CICOCO. The reaction is carried out in the presence or absence of an inert organic solvent, for example in aliphatic, halogenated aliphatic, aromatic or halogenated aromatic hydrocarbons, for example n-hexane, benzene, toluene, xylenes, dichloromethane, 1,2-dichloroethane or chiorobenzene, at reaction temperatures in the range of from −20° C. to the reflux temperature of the reaction mixture, preferably at 40-150° C., and in the presence of a catalytic amount of N,N-dimethylformamide. Such reactions are generally known and described in the literature in various variations with respect to the leaving group X.

The compounds of the formulae III, IV, V and VI are known and can be prepared analogously to the methods described, for example, in WO 92/07837, DE-A-3818958, EP-A-0 338 992 and DE-A-3902818.

The compounds of the formula XII in reaction scheme 2 can be obtained by standard processes, for example from the corresponding compounds of the formula II

in which R and m are as defined above and X is a leaving group, for example halogen, for example via Claisen condensation, or from the compounds of the formula II by reaction with a ketocarboxylic acid salt of the formula XV

in which R

36

is as defined under formula I and M

+

is an alkali metal ion (cf., for example, WO 96/26192).

The compounds of the formulae II and XI are known and can be prepared analogously to the methods described, for example, in WO 97146530, EP-A-0 353 187, Heterocycles, 48, 779 (1998), Heterocycles, 46, 129 (1997), or Tetrahedron Letters, 1749 (1998).

For preparing all other compounds of the formula I functionalized according to the definition of (R)

m

, there is a large number of known standard processes available, for example alkylation, halogenation, acylation, amidation, oximation, oxidation and reduction, and the choice of the suitable preparation processes depends on the properties (reactivities) of the substituents in the intermediates in question.

All further compounds originating from the scope of the formula I can be prepared in a simple manner, taking into account the chemical properties of the pyridyl or Q moiety.

The end products of the formula I can be isolated in a customary manner by concentration or evaporation of the solvent and be purified by recrystallization or trituration of the solid residue in solvents in which they are only sparingly soluble, such as ethers, aromatic hydrocarbons or chlorinated hydrocarbons, by distillation or by means of column chromatography and a suitable mobile phase.

Furthermore, it is known to the person skilled in the art in which order certain reactions have to be carried out advantageously to avoid possible side reactions. Unless a targeted synthesis is carried out for isolating pure isomers, the product may be obtained as a mixture of two or more isomers. The isomers can be separated by methods known per se.

Compounds of the formula I in which p is 1, i.e. the corresponding N-oxides of the formula I, can be prepared by reacting a compound of the formula I in which p is 0 with a suitable oxidizing agent, for example with the H

2

O

2

urea adduct, in the presence of an acid anhydride, for example trifluoroacetic anhydride. This reaction sequence is demonstrated using the example of group Q

2

below:

Compounds of the formula I in which R in the ortho position to the pyridine nitrogen is 1-chloro-C

1

-C

2

alkyl, 1-hydroxy-C

1

-C

2

alkyl, 1-(C

1

-C

6

alkylcarbonyloxy)-C

1

-C

2

alkyl, 1 -benzoyloxy-C

1

-C

2

alkyl, 1-(C

1

-C

4

alkoxycarbonyloxy)-C

1

-C

2

alkyl, 1-(C

1

-C

4

alkylthio)-C

1

-C

2

alkyl, 1-(C

1

-C

4

-alkylsulfinyl)-C

1

-C

2

alkyl, 1-(C

7

-C

4

alkylsulfonyl)-C

1

-C

2

alkyl, 1-thiocyanato-C

1

-C

2

alkyl, 1-cyano-C

1

-C

2

alkyl, can also be prepared, for example, by heating an N-oxide of the formula I under known reaction conditions, for example in the presence of tosyl chloride (see, for example, Parham, W. E.; Sloan, K. B.; Reddy, K. R.; Olson, P. E.;

J Org Chem

1973, 38, 927) or in the presence of an acid anhydride (see, for example, Konno, K.; Hashimoto, K.; Shirahama, H.; Matsumoto, T.;

Heterocycles

1986, 24, 2169), followed, if appropriate, by subsequent conversion.

The compounds of the formula XXIIa are synthesized analogously to known processes, for example those mentioned in Heterocycles, 46, 129 (1997) or Helvetica Chimica Acta 71, 596 (1988), and comprises either

a) acylating a compound of the formula XVI

in which R

301

is hydrogen or C

1

-C

6

alkyl;

R

401

is hydrogen, C

1

-C

6

alkyl C

2

-C

6

alkenyl, C

3

-C

6

cycloalkyl, C

1

-C

6

alkoxy, C

1

-C

6

alkylthio, C

1

-C

6

alkylsulfinyl, C

1

-C

6

haloalkyl, 1-(C

1

-C

6

alkylcarbonyloxy)-C

1

-C

6

alkyl, 1-(C

1

-C

6

alkylthio)-C

1

-C

6

-alkyl, 1-(C

1

-C

6

alkylsulfinyl)-C

1

-C

6

alkyl, 1-(C

1

-C

6

alkylsulfonyl)-C

1

-C

6

alkyl, 1-thiocyanato-C

1

-C

6

-alkyl, 1-cyano-C

1

-C

6

alkyl, phenyl, where the phenyl groups may be mono- or polysubstituted by halogen, methyl, ethyl, trifluoromethyl, methoxy or nitro, or is a five- to ten-membered monocyclic or fused bicyclic ring system which may be aromatic or partially saturated and may contain 1 to 4 heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur, where the ring system is either attached directly or via a C

1

-C

4

alkylene group to the double bond, and each ring system may not contain more than 2 oxygen atoms and not more than two sulfur atoms and the ring system for its part may be mono-, di- or trisubstituted by C

1

-C

6

alkyl, C

1

-C

6

haloalkyl, C

3

-C

6

alkenyl, C

3

-C

6

haloalkenyl, C

3

-C

6

alkynyl, C

3

-C

6

haloalkynyl, C

1

-C

6

alkoxy, C

1

-C

6

haloalkoxy, C

3

-C

6

alkenyloxy, C

3

-C

6

alkynyloxy, mercapto, C

1

-C

6

alkylthio, C

1

-C

6

haloalkylthio, C

3

-C

6

alkenylthio, C

3

-C

6

haloalkenylthio, C

3

-C

6

alkynylthio, C

2

-C

5

alkoxyalkylthio, C

3

-C

5

acetylalkylthio, C

3

-C

6

alkoxycarbonylalkylthio, C

2

-C

4

cyanoalkylthio, C

1

-C

6

alkylsulfinyl, C

1

-C

6

haloalkylsulfinyl, C

1

-C

6

alkylsulfonyl, C

1

-C

6

haloalkylsulfonyl, aminosulfonyl, C

1

-C

2

alkylaminosulfonyl, C

2

-C

4

dialkylaminosulfonyl, C

1

-C

3

alkylene-R

87

, NR

88

R

89

, halogen, cyano, nitro, phenyl and benzylthio, where phenyl and benzylthio for their part may be substituted on the phenyl ring by C

1

-C

3

alkyl, C

1

-C

3

haloalkyl, C

1

-C

3

alkoxy, C

1

-C

3

-haloalkoxy, halogen, cyano or nitro and where substituents on nitrogen in the heterocyclic ring are different from halogen;

R

87

is C

1

-C

3

alkoxy, C

2

-C

4

alkoxycarbonyl, C

1

-C

3

alkylthio, C

1

-C

3

alkylsulfinyl, C

1

-C

3

alkylsulfonyl or phenyl, where phenyl for its part may be substituted by C

1

-C

3

alkyl, C

1

-C

3

haloalkyl, C

1

-C

3

-alkoxy, C

1

-C

3

haloalkoxy, halogen, cyano or nitro;

R

88

is hydrogen or C

1

-C

6

alkyl and

R

89

is C

1

-C

6

alkyl or C

1

-C

6

alkoxy;

with a compound of the formula XVII

in which R

501

is C

1

-C

6

haloalkyl and X

2

is O(CO)R

501

or halogen to give the compound of the formula XVIII

in which R

301

, R

401

, R

501

, and R

14

are as defined above, in the presence of a base, for example an aromatic amine, for example pyridine, and subsequently replacing the alkoxy group by the amino group using ammonia in an organic solvent, for example a halogenated hydrocarbon, for example dichloromethane, or a nitrile, for example acetonitrile. The resulting compound of the formula XIX

is subsequently condensed with a compound of the formula XX

in which R

201

is C

1

-C

6

alkyl, C

2

-C

6

alkenyl, C

2

-C

6

haloalkenyl, C

2

-C

6

alkynyl, C

2

-C

6

-haloalkynyl, C

3

-C

6

cycloalkyl, C

1

-C

6

haloalkyl, 1-(C

1

-C

6

alkylcarbonyloxy)-C

1

-C

6

alkyl, 1-(C

1

-C

6

alkylthio)-C

1

-C

6

alkyl, 1-(C

1

-C

6

alkylsulfinyl)-C

1

-C

6

alkyl, 1-(C

1

-C

6

alkylsulfonyl)C

1

-C

6

alkyl, 1-thiocyanato-C

1

-C

6

alkyl, 1-cyano-C

1

-C

6

alkyl, C

1

-C

6

alkoxy-C

1

-C

6

alkyl, C

1

-C

6

alkoxycarbonyl-C

1

-C

6

alkoxy, C

1

-C

6

alkylthio-C

1

-C

6

alkoxy, phenyl, benzyl, phenoxy, phenylthio, phenylsulfinyl, phenylsulfonyl, benzyithio, benzylsulfinyl or benzylsulfonyl, where the phenyl groups may be mono- or polysubstituted at least by halogen, methyl, ethyl, trifluoromethyl, methoxy or nitro, or is a five- to ten-membered monocyclic or fused bicyclic ring system which may be aromatic or partially saturated and may contain 1 to 4 heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur, where the ring system is attached either directly or via a C

1

-C

4

-alkylene group and each ring system may not contain more than 2 oxygen atoms and not more than two sulfur atoms, and the ring system for its part may be mono-, di- or trisubstituted by C

1

-C

6

alkyl, C

1

-C

6

haloalkyl, C

3

-C

6

alkenyl, C

3

-C

6

haloalkenyl, C

3

-C

6

alkynyl, C

3

-C

6

haloalkynyl, C

1

-C

6

a lkoxy, C

1

-C

6

haloalkoxy, C

3

-C

6

alkenyloxy, C

3

-C

6

alkynyloxy, mercapto, C

1

-C

6

alkylthio, C

1

-C

6

haloalkylthio, C

3

-C

6

alkenylthio, C

3

-C

6

haloalkenylthio, C

3

-C

6

alkynylthio, C

2

-C

5

alkoxyalkylthio, C

3

-C

5

acetylalkylthio, C

3

-C

6

alkoxycarbonylalkylthio, C

2

-C

4

cyanoalkylthio, C

1

-C

6

alkylsulfinyl, C

1

-C

6

haloalky lsulfinyl, C

1

-C

6

alkylsulfonyl, C

1

-C

6

haloalkylsulfonyl, aminosulfonyl, C

1

-C

2

alkylaminosulfonyl, C

2

-C

4

dialkylaminosulfonyl, C

1

-C

3

-R

90

, NR

91

R

92

, halogen, cyano, nitro, phenyl and benzylthio, where phenyl and benzylthio for their part may be substituted on the phenyl ring by C

1

-C

3

alkyl, C

1

-C

3

haloalkyl, C

1

-C

3

alkoxy, C

1

-C

3

-haloalkoxy, halogen, cyano or nitro, and where substituents on nitrogen in the heterocyclic ring are different from halogen;

R

90

is C

1

-C

3

alkoxy, C

2

-C

4

alkoxycarbonyl, C

1

-C

3

alkylthio, C

1

-C

3

alkylsuffinyl, C

1

-C

3

alkylsulfonyl or phenyl, where phenyl for its part may be substituted by C

1

-C

3

-alkyl, C

1

-C

3

haloalkyl, C

1

-C

3

-alkoxy, C

1

-C

3

haloalkoxy, halogen, cyano or nitro;

R

91

is hydrogen or C

1

-C

6

alkyl and

R

92

is C

1

-C

6

alkyl or C

1

-C

6

alkoxy and

R

14

is as defined above, and the resulting compound of the formula XXIa

is subsequently hydrolysed to give the compound of the formula XXIIa

in which R

201

, R

301

, R

401

, and R

501

are as defined above, or

b) condensing a compound of the formula XXIII

in which R

14

is as defined above with a compound of the formula XXIV

and chlorinating the resulting compound of the formula XXV

in which R

301

, R

401

and R

501

are as defined above and R

14

is C

1

-C

4

alkyl to give compounds of the formula XXVI

in which R

301

, R

401

, R

501

and R

14

are as defined above (using, for example, POCI

3

), and subsequently reacting this compound with a nucleophile of the formula XXVII

Z—R

150

(XXVII)

In which Z is SH, OH or amino and R

150

is C

1

-C

6

alkyl, C

3

-C

6

alkeny4 C

3

-C

6

halogenalkenyl, C

3

C

6

alkynyl, C

3

-C

6

haloalkynyl, C

1

-C

6

alkylsulfonyl, C

1

-C

6

haloalkyl, phenyl, benzyl, where the phenyl and benzyl groups for their part may be substituted by C

1

-C

3

alkyl, C

1

-C

3

haloalkyl, C

1

-C

3

alkoxy, C

1

-C

3

haloalkoxy, halogen, cyano or nitro, is C

1

-C

1

alkoxy-C

1

-C

4

alkyl or C

1

-C

4

-alkylthio-C

1

-C

4

alkyl, C

1

-C

4

alkylsulfinyl-C

1

-C

4

alkyl, C

1

-C

4

alkylsulfonyl-C

1

-C

4

alkyl, or a five- to ten-membered monocyclic or fused bicyclic ring system which may be aromatic or partially saturated and may contain 1 to 4 heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur, and each ring system may not contain more than 2 oxygen atoms and not more than two sulfur atoms, and the ring system for its part may be mono-, di- or trisubstituted by C

1

-C

6

alkyl, C

1

-C

6

haloalkyl, C

3

-C

6

alkenyl, C

3

-C

6

haloalkenyl, C

3

-C

6

-alkynyl, C

3

-C

6

haloalkynyl, C

1

-C

6

alkoxy, C

1

-C

6

haloalkoxy, C

3

-C

6

alkenyloxy, C

3

-C

6

alkynyloxy, mercapto, C

1

-C

6

alkylthio, C

1

-C

6

haloalkylthio, C

3

-C

6

alkenylthio, C

3

-C

6

haloalkenylthio, C

3

-C

6

-alkynylthio, C

2

-C

5

alkoxyalkylthio, C

3

-C

5

acetylalkylthio, C

3

-C

6

alkoxycarbonylalkylthio, C

2

-C

4

-cyanoalkylthio, C

1

-C

6

alkylsulfinyl, C

1

-C

6

haloalkylsulfinyl, C

1

-C

6

alkylsulfonyl, C

1

-C

6

-haloalkylsulfonyl, aminosulfonyl, C

1

-C

2

alkylaminosulfonyl, C

2

-C

4

dialkylaminosulfonyl, C

1

-C

3

-alkylene-R

93

, NR

94

R

95

, halogen, cyano, nitro, phenyl and benzylthio, where phenyl and benzylthio for their part may be substituted on the phenyl ring by C

1

-C

3

alkyl, C

1

-C

3

-haloalkyl, C

1

-C

3

alkoxy, C

1

-C

3

haloalkoxy, halogen, cyano or nitro, and where substituents on nitrogen in the heterocyclic ring are different from halogen;

R

93

is C

1

-C

3

alkoxy, C

2

-C

4

alkoxycarbonyl, C

1

-C

3

alkylthio, C

1

-C

3

alkylsulfinyl, C

1

-C

3

alkylsulfonyl or phenyl, where phenyl for its part may be substituted by C

1

-C

3

alkyl, C

1

-C

3

haloalkyl, C

1

-C

3

alkoxy, C

1

-C

3

haloalkoxy, halogen, cyano or nitro;

R

94

is hydrogen or C

1

-C

6

alkyl and

R

95

is C

1

-C

6

alkyl or C

1

-C

6

alkoxy;

in the presence of a base to give compounds of the formula XXIb

in which R

14

, R

150

, R

301

, R

401

, and R

501

are as defined above, and subsequen tly hydrolysing the resulting compound to give the compound of the formula XXIIb

in which R

150

, R

301

, R

401

and R

501

are as defined.

Compounds of the formula XXIb in which R

150

is fluorine are prepared by reacting a compound of the formula XXVI in the presence of a polar aprotic solvent, for example acetonitrile, dimethylformamide or sulfolane, with potassium fluoride in the presence or absence of a catalytic amount of 18-crown-6. Compounds of the formula XXIc in which R

150

is hydrogen are preparerd by reducing the chlorine group in the formula XXVI, for example using hydrogen in the presence of a suitable metal catalyst or using ammonium formate in a suitable solvent. The preparation of the compounds of the formula XXIIa, or XXIIb and XXIIc is illustrated in more detail in the reaction schemes 4 and 5 below.

For preparing all other compounds of the formula I which are functionalized according to the definition of R

201

(R

150

) to R

501

, a large number of known standard processes is suitable, for example alkylation, halogenation, acylation, amidation, oximation, oxidation and reduction, the choice of the suitable preparation processes depending on the properties (reactivities) of the substituents in the intermediates in question.

The novel compounds of the formula IIb in which R

f

is trifluoromethyl, difluorochloromethyl, pentafluoroethyl, heptafluoro-n-propyl or trichloromethyl, R

X1

is C

1

-C

6

alkyl and Q and R are as defined under formula I can be prepared by generally known processes via 3-alkoxycarbonyl-4-perhaloalkylpyridine N-oxides of the formula XXVIII according to reaction scheme 5 by preparing, using suitable chlorination conditions and separation processes, the 6-chloro-4-haloalkyl-3-nicotinic esters of the formula XXX and then converting these compounds with a nucleophile of the formula XXXI

Z

01

—R

151tm (XXXI)

in which Z

07

is SH, hydroxyl, halogen or amino and R

151

is hydrogen, C

1

-C

6

alkyl, C

3

-C

6

-alkenyl, C

3

-C

6

haloalkenyl, C

3

-C

6

alkynyl, halogen, C

3

-C

6

haloalkynyl, C

1

-C

6

alkylsulfonyl, C

1

-C

6

-haloalkyl, phenyl, benzyl, where the phenyl and benzyl groups for their part may be substituted by C

1

-C

3

alkyl, C

1

-C

3

haloalkyl, C

1

-C

3

alkoxy, C

1

-C

3

haloalkoxy, halogen, cyano or nitro, is C

1

-C

4

alkoxy-C

1

-C

4

alkyl or C

1

-C

4

alkylthio-C

1

-C

4

alkyl , C

1

-C

4

alkylsulfinyl-C

1

-C

4

alkyl, C

1

-C

4

alkylsulfonyl-C

1

-C

4

alkyl, or a five- to ten-membered monocyclic or fused bicyclic ring system which may be aromatic or partially saturated and may contain 1 to 4 heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur, and each ring system may not contain more than 2 oxygen atoms and not more than two sulfur atoms, and the ring system for its part may be mono-, di- or trisubstituted by

C

1

-C

6

alkyl, C

1

-C

6

haloalkyl, C

3

-C

6

alkenyl, C

3

-C

6

haloalkenyl, C

3

-C

6

alkynyl, C

3

-C

6

-haloalkynyl, C

1

-C

6

alkoxy, C

1

-C

6

haloalkoxy, C

3

-C

6

alkenyloxy, C

3

-C

6

alkynyloxy, mercapto, C

1

-C

6

alkylthio, C

1

-C

6

haloalkylthio, C

3

-C

6

alkenylthio, C

3

-C

6

haloalkenylthio, C

3

-C

6

alkynylthio, C

2

-C

5

alkoxyalkylthio, C

3

-C

5

acetylalkylthio, C

3

-C

6

alkoxycarbonylalkylthio, C

2

-C

4

cyanoalkylthio, C

l

-C

6

-alkylsulfinyl, C

1

-C

6

haloalkylsulfinyl, C

1

-C

6

alkylsulfonyl, C

1

-C

6

haloalkylsulfonyl, aminosulfonyl, C

1

-C

2

alkylaminosulfonyl, C

2

-C

4

dialkylaminosulfonyl, C

1

-C

3

alkylene-R

96,

NR97R

98

, halogen, cyano, nitro, phenyl or benzylthio, where phenyl and benzylthio for their part may be substituted on the phenyl ring by C

1

-C

3

alkyl, C

1

-C

3

haloalkyl, C

1

-C

3

alkoxy, C

1

-C

3

-haloalkoxy, halogen, cyano or nitro,

R

96

is C

1

-C

3

alkoxy, C

2

-C

4

alkoxycarbonyl, C

1

-C

3

alkylthio, C

1

-C

3

alkylsulfinyl, C

1

-C

3

alkylsulfonyl or phenyl, where phenyl for its part may be substituted by C

1

-C

3

alkyl, C

1

-C

3

haloalkyl, C

1

-C

3

-alkoxy, C

1

-C

3

haloalkoxy, halogen, cyano or nitro;

R

97

is hydrogen or C

1

-C

6

alkyl and

R

98

is C

1

-C

6

alkyl or C

1

-C

6

alkoxy;

and where substituents on nitrogen in the heterocyclic ring are different from halogen, using reaction processses which are generally known to the person skilled in the art, into the 6-substituted 4-perhaloalkylnicotinic acids of the formula XXXII and their subsequent products of the formulae IIb and Ib as described in reaction scheme 1. This is shown in reaction scheme 6 below.

According to this reaction scheme, it is preferably possible to prepare the compounds of the formula I with the group Q

1

in which R

20

is hydroxyl, the compounds of the formula I with the group 02 in which R

23

is hydroxyl, the compounds of the formula I with the group Q

3

in which R

26

is hydroxyl and the compounds of the formula I with the group Q

4

in which R

30

is hydroxyl.

6-substituted 2-haloalkylnicotinic acid compounds of the formula Ic can be prepared, for example, from the corresponding 2-haloalkyl-3-alkoxycarbonyl-2-pyridines XXXIII in which R

f

is trifluoromethyl, difluorochloromethyl, pentafluoroethyl, heptafluoro-n-propyl or trichioromethyl and R

1x

is C

1

-C

6

alkyl and R is as defined under formula I, by hydrolysis into the corresponding carboxylic acids and their subsequent activation, for example by conversion into an acylhalide (IIc). (Reaction scheme 7).

Their precursors of the formulae XXXIIIa, XXXIIIb, XXXIIIc, XXXIIId, XXXIIIe, XXXIIIf, XXXIIIg and XXXIIIh are likewise accessible by conversion processes known to the person skilled in the art (reaction shceme 7). 2-Trifluoromethyl-3-ethoxycarbonyl-2-pyridone (formula XXXIIIa in which R is hydrogen, R

1X

is ethyl and Rf is trifluoromethyl) in particular is known form Org. Process Research & Developmnet, 1, 370 (1997).

Intermediates of the formulae XXXIIIa to XXXIIIh can be obtained by reacting, for example for preparing a 6-halo derivative of the formula XXXIIId, a pyridone of the formula XXXIIIa (preparation according to Org. Process Research & Development, 1, 370 (1997) or scheme 8) with a halogenating agent, for example phosphorus oxychloride, phosphorus oxybromide or phenyl dichlorophosphate, in the presence or absence of added base, such as a dialkylaniline, in the presence or absence of solvent, if desired in a pressure vessel, at temperatures between 0 and 220° C. (preferably 60-200° C.). It is known to the person skilled in the art how to convert chloro derivatives by nucleophilic substitution, for example using an alkali metal iodide in an inert solvent into the corresponding iodides, or using gaseous hydrobromic acid in lower carboxylic acids, for example conc. acetic acid, into the corresponding bromo derivatives (for example according to U.S. Pat. No. 3,974,166) or using alkali metal fluoride in a dipolar solvent, such as sulfolane, into the corresponding fluoro derivatives.

The compound of the formula XXXIIIe can be prepared by reacting a halo derivative of the formula XXXIIId obtained as described above with an alcohol of the formula R

151

—OH in the presence of a base, such as sodium hydride, or an alkali metal oxide or carbonate, or directly with an alkali metal alkoxide, in an inert solvent such as dimethylformamide or in an excess of the alcohol of the formula R

151

—OH which corresponds to the group to be introduced, at temperatures between −5 and 160° C., or by reacting, to prepare a corresponding 6-thioether of the formula XXXIIIc, analogously to what was described above, either the halide of the formula XXXIIId with a thiol of the formula R

151

—SH in the presence of a base such as sodium hydride or with an alkali metal salt of a thiol in an inert solvent at −10-150° C., or by preparing, starting from a pyridone XXXIIIa and using a thionating agent, for example Lawesson's reagent, in an inert solvent, such as toluene or acetonitrile, a pyrithione of the formula XXXIIIb and alkylating this with an alkylating agent R

151

-X, where X is a leaving group, such as halide (Cl, Br, I) or ROSO

3

— or RSO

2

—, at 20-120° C. in an inert solvent, such as tetrahydrofuran, to give the thioether of the formula XXXIIIc, or, to prepare the corresponding sulfinyl or sulfonyl derivative of the formula XXXIIIf, reacting with an oxidizing agent, such as m-chloroperbenzoic acid or sodium periodate, or sodium perborate, under temperature control known to the person skilled in the art, depending on the degree of oxidation (for example −30° C.-+50° C. for m

01

=1 or −20° C.-+100° C. for m

01

=2) in an inert solvent, such as dichloromethane, to give XXXIIIf, or, to prepare 6-alkyl derivatives XXXIIIg according to the invention, reacting a sulfone of the formula XXXIIIf (m

01

=2) or a halo derivative of the formula XXXIIId in the presence or absence of a Pd(O) catalyst such as Pd(PPh

3

)

2

Cl

2

with a tetra-C

1

-C

6

alkyltin or with a Grignard reagent C

1

-C

6

alkyl-MgHal at temperatures between −10° and 180° C., for example analogously to Synlett 1998 (1185), or as described in Organocopper Reagents, R. J. K. Taylor, Oxford University Press 1994, or in Transition Metals in Organic Synthesis, S. Gibson, Oxford Univ. Press,1997, or in Org. React. 50, 1 (Stille reaction), or, to prepare 6-cyano derivatives of the formula XXXIIIh, reacting a halide of the formula XXXIIId or a sulfone of the formula XXXIIIf (m

01

=2) with an alkali metal or tetraalkylammonium cyanide or copper cyanide in an inert solvent, such as dichloromethane, tetrahydrofuran or dimethylformamide, at temperatures between 0° C. and 220° C.

Some of the compounds of the formula XXXIIIe are also obtainable from the pyridone of the formula XXXIIIa by reacting them analogously to Org. React. 42, 2 with an alcohol R

151

OH in the presence of an azodicarboxylic ester (for example diethyl ester) and triphenylphosphine in an inert solvent, such as tetrahydrofuran or dioxane. (Scheme 9)

The intermediates of the formula XXXIIIa required in reaction scheme 8 as starting materials are obtainable according to Scheme 10 route A or route B (Org. Process Research & Development, 1, 370 (1997)) or route C.

Intermediates of the formula XXXIIIa are obtainable by route A by reacting, to prepare the 3,4-dihydro-5-alkoxycarbonyl-6-haloalkylpyridin-2-ones of the formula XXXVIII, an enamine of the formula XXXV in the presence or, preferably, in the absence of a solvent either in an excess of enamine or in the presence of a base, such as a tert-amine, with an acryloyl chloride of the formula XXXIV at temperatures between −10° and +200° C., or by reacting a keto ester of the formula XXXVII with an acrylamide of the formula XXXVI in the presence of a catalyst such as p-toluenesulfonic acid (=HOTs) in an inert solvent, such as toluene, at temperatures between 30 and 200° C., with removal of the water of reaction formed (for example azeotropic distillation), or by reacting a keto ester of the formula XXXVII in the presence of a base, such as an alkali metal alkoxide or magnesium alkoxide, with a 4-haloketo ester of the formula XXXIX in an inert solvent, such as ethanol, at 0-180° C. to give the intermediate of the formula XXXX, converting this with ammonia or an ammonium salt, such as ammonium acetate, or with a bis-silylamine such as hexamethyldisilazane, in the presence or absence of an acidic catalyst, such as sulfuric acid or p-toluenesulfonic acid or an organic carboxylic acid (for example conc. acetic acid), in an inert solvent and at temperatures between 0° and 180° C. into the corresponding enamine of the formula XXXXI, subsequently cyclizing in the presence of a catalyst, such as p-toluenesulfonic acid or sulfuric acid, if desired with continuous removal of the water of reaction formed in an inert solvent, such as toluene, to give the dihydropyridone of the formula XXXVIII, and finally treating with an oxidizing agent, such as manganese dioxide, in an inert solvent, such as chlorobenzene, at temperatures between 50 and 250° C., to prepare the pyridones XXXIIIa.

The intermediates of the formula IIa

in which Q

a

is hydroxyl, halogen, cyano, or a group —CH

2

(CO)R

36

or

R

b

is hydrogen, C

1

-C

4

alkyl or halogen;

R

1

is trifluoromethyl, difluorochloromethyl, pentafluoroethyl, heptafluoro-n-propyl or trichloromethyl;

R

a

is C

1

-C

3

alkyl, C

1

-C

3

haloalkyl, C

3

-C

4

cycloalkyl, C

1

-C

2

alkoxy-C

1

-C

4

alkyl, C

1

-C

2

-alkylthiomethyl, hydroxyl, halogen, cyano, C

1

-C

3

alkoxy, C

1

-C

3

haloalkoxy, allyloxy, propargyioxy, C

1

-C

3

alkylthio, C

1

-C

3

alkylsulfinyl, C

1

-C

3

alkylsulfonyl or C

1

-C

3

alkylsulfonyloxy, and R

01

and R

36

are as defined under group O

5

of the formula 1, except for the compounds 2,6-bistrifluoromethyinicotinic acid, 2,6-bistrifluoromethyl-5-methoxynicotinic acid and 2-hydroxy-6-trifluoromethyinicotinic acid, are novel and therefore likewise form part of the subject matter of the present invention.

Compounds of the formula IIb

in which Q

b

is hydroxyl, halogen, cyano or a group —CH

2

(CO)R

99

or

R

99

is C

1

-C

4

alkyl, C

1

-C

4

haloalkyl, C

3

-C

4

cycloalkyl or C

1

-C

4

alkoxy;

R

f

is trifluoromethyl, difluorochloromethyl, pentafluoroethyl or heptafluoro-n-propyl; and

R

c

is C

1

-C

3

alkyl, C

1

-C

3

haloalkyl, C

1

-C

2

alkoxymethyl, C

1

-C

1

alkylthiomethyl, hydroxyl, halogen, cyano, C

1

-C

3

alkoxy, C

1

-C

3

haloalkoxy, allyloxy, propargyloxy, C

1

-C

3

alkylthio, C

1

-C

3

-alkylsulfinyl, C

1

-C

3

alkylsulfonyl or C

1

-C

3

alkylsulfonyloxy and R

01

is as defined under formula I are novel and therefore likewise form part of the subject matter of the present invention.

Preferred compounds of the formula Ila correspond to the formula Ia

in which Q

a

is hydroxyl, halogen , cyano or a group —CH

2

(CO)R

36

or

R

01

and R

36

are as defined in claim 1 and R

a

is C

1

-C

3

alkyl.

The compounds of the formula I or compositions comprising them can be used according to the invention in all the application methods customary in agriculture, for example pre-emergence application, postemergence application and seed dressing, and various methods and techniques, for example controlled release of active compounds. To this end, the active compound is absorbed in solution onto mineral granule carriers or polymerized granules (urea/formaldehyde) and dried. If appropriate, a coating which allows the active compound to be released in metered form over a certain period of time can additionally be applied (coated granules).

The compounds of the formula I can be employed as herbicides in unchanged form, i.e. as they are obtained in the synthesis, but they are preferably processed in a customary manner with the auxiliaries conventionally used in the art of formulation, for example to give emulsifiable concentrates, directly sprayable or dilutable solutions, dilute emulsions, wettable powders, soluble powders, dusts, granules or microcapsules. Such formulations are described, for example, in WO 97/34485 on pages 9 to 13. The methods of application, such as spraying, atomizing, dusting, wetting, scattering or watering, in the same way as the nature of the compositions, are chosen according to the aims striven for and the given circumstances.

The formulations, i.e. the compositions, formulations or preparations comprising the active compound of the formula I or at least one active compound of the formula I and as a rule one or more solid or liquid formulation auxiliaries, are prepared in a known manner, for example by intimate mixing and/or grinding of the active compounds with the formulation auxiliaries, for example solvents or solid carriers. Surface-active compounds (surfactants) can furthermore additionally be used during the preparation of the formulations. Examples of solvents and solid carriers are given, for example, in WO 97/34485 on page 6. Depending on the nature of the active compound of the formula I to be formulated, suitable surface-active compounds are nonionic, cationic and/or anionic surfactants and surfactant mixtures having good emulsifying, dispersing and wetting properties.

Examples of suitable anionic, nonionic and cationic surfactants are listed, for example, in WO 97/34485 on pages 7 and 8.

The surfactants conventionally used in the art of formulation and which are suitable to prepare the herbicidal compositions according to the invention are described, inter alia, in “Mc Cutcheon's Detergents and Emulsifiers Annual”, MC Publishing Corp., Ridgewood N.J., 1981, Stache, H., “Tensid-Taschenbuch” [Surfactant handbook], Carl Hanser Verag, Munich/Vienna, 1981 and M. and J. Ash, “Encyclopedia of Surfactants”, Vol I-III, Chemical Publishing Co., New York, 1980-81.

The herbicidal formulations as a rule comprise 0.1 to 99% by weight, in particular 0.1 to 95% by weight, of herbicide, 1 to 99.9% by weight, in particular 5 to 99.8% by weight, of a solid or liquid formulation auxiliary and 0 to 25% by weight, in particular 0.1 to 25% by weight, of a surfactant. While concentrated compositions are rather preferred as commercial goods, the end user as a rule uses dilute compositions. The compositions can also comprise further additives, such as stabilizers, for example epoxidized or non-epoxidized vegetable oils (epoxidized coconut oil, rapeseed oil or soya oil), defoamers, for example silicone oil, preservatives, viscosity regulators, binders, tackifiers and fertilizers or other active compounds.

The active compounds of the formula I are as a rule applied to the plants or their habitat, at application rates of 0.001 to 4 kg/ha, in particular 0.005 to 2 kg tha. The dosage required for the desired effect can be determined by tests. It depends on the nature of the effect, the development stage of the crop plant and the weed and on the application (location, time, process) and can, as a function of these parameters, vary within wide ranges.

The compounds of the formula I have herbicidal and growth-inhibiting properties, owing to which they can be used in crops of useful plants, in particular in cereals, cotton, soya, sugar beet, sugar cane, plantings, rapeseed, maize and rice, and for the non-selective control of weeds. Crops include those which have been rendered tolerant towards herbicides or herbicide classes by conventional breeding methods or genetical engineering methods. The weeds to be controlled can be both monocotyledonous and dicotyledonous weeds, for example Stellaria, Nasturtium, Agrostis, Digitaria, Avena, Setaria,Sinapis, Lolium, Solanum, Echinochloa, Scirpus, Monochoria, Sagittaria, Bromus, Alopecurus,

Sorghum halepense,

Rottboellia, Cyperus, Abutilon, Sida, Xanthium, Amaranthus, Chenopodium, Ipomoea, Chrysanthemum, Galium, Viola and Veronica.

The examples below illustrate the invention in more detail, without limiting it.

PREPARATION EXAMPLES

Example H1

PreParation of 2-difluoromethoxy-6-trifluoromethylnicotinic acid

At 70° C., 25 g (0.106 mol ) of (3-(ethoxycarbonyl)-6-trifluoromethyl)pyrid-2-one (Helv. Chim. Acta (1988), 71(3), 596 601) in a mixture of 50 ml of dimethylformamide and 20 ml of water are treated, in the presence of 16 g (0.116 mol) of finely powdered potassium carbonate and with efficient stirring, with a continuous stream of gaseous Freon-22. After 6 hours, a further 16 g of potassium carbonate and 20 ml of dimethyl sulfoxide are added, and the mixture is stirred with continuous introduction of Freon-22 gas at a temperature of 100° C for another 4 hours. The mixture is then treated with water and ice and extracted with diethyl ether. The aqueous phase is adjusted to pH 2 using conc. HCl and extracted with ethyl acetate. Diethyl ether is added to the extract, and some (3-(carboxy)-6-trifluoromethyl)pyrid-2-one crystals which have precipitated out are removed by filtration. The filtrate is filtered through a silica gel column (mobile phase ethyl acetate/hexane 1:1) giving, as a crystalline product, pure 2-difluoromethoxy-6-trifluoromethylnicotinic acid:

1

H NMR (CDCl

3

, ppm): 8.60, d, J=9 Hz, 1H; 7.62, d, J=9 Hz, 1H; 7.62, t, J=67 Hz, 1H.

Example H2

Preparation of 4-methyl-6-trifluoromethylnicotinic Acid

In the presence of 5.8 ml of phenyl dichlorophosphate, 7.5 g (0.03 mol) of ((3-ethoxycarbonyl)-4-methyl-6-trifluoromethyl)pyrid-2-one (Helv. Chim. Acta (1988), 71 (3), 596-601) are heated in a pressure vessel at a temperature of 170° C. for 3 hours. The cold reaction solution is filtered directly through a short silica gel column (mobile phase: ethyl acetate/hexane 1:9), giving, as an oily product, ethyl 2-chloro-4-methyl-6-trifluoromethylpyridin-3-ylcarboxylate:

1

H NMR (CDCl

3

, ppm): 7.49, s, 1H; 4.48, q, 2H; 2.43, s, 3H, 1.43, t, 3H.

3.0 g (16.8 mmol) of the above product and, in 2 portions, a total of 5 g of ammonium formate are added to a suspension of 0.55 g of 10% Pd/C in 20 ml of methanol, and the mixture is stirred at room temperature for 24 hours. The reaction mixture is then filtered through Celite and, after addition of sodium chloride solution, extracted with ethyl acetate. Chromatographic purification (mobile phase 1:9) gives the 4-methyl-6-trifluoromethylpyridin-3-yl ethyl ester as an oil:

1

H NMR (CDCl

3

, ppm): 9.11, s, 1H; 7.56, s, 1H, 4.44, q, 2H; 2.72, s, 3H, 1.42, t, 3H. This is hydrolysed at 40° C. in the presence of aqueous potassium hydroxide solution in dioxane. Extraction with ethyl acetate gives, after acidification to pH 2.7, 4-methyl-6-trifluoromethyinicotinic acid as a crystalline product:

1

H NMR (CDCl

3

, ppm): 7.49, s, 1H; 4.48, q, 2H; 2.43, s, 3H, 1.43, t, 3H; 9.32, s, 1 H, 7.62, s, 1 H, 2.79, s, 3H.

Example H3

Preparation of 6-chloro-4-trifluoromethylnicotinic Acid

9.6 g (0.047 mol) of methyl 4-trifluoromethylpyridin-3-ylcarboxylate, dissolved in 50 ml of dichloromethane, are treated with 30% hydrogen peroxide/urea adduct and 17 ml of trifluoroacetic anhydride. The reaction solution is stirred at temperature of 20° C. for 20 hours and then washed once each with dilute sodium hydroxide solution and half-saturated sodium chloride solution. The product obtained is 3-methoxycarbonyl4-trifluoromethyl-3-pyridine N-oxide;

1

H NMR (CDCl

3

, ppm): 8.55, s, 1H; 8.31, d, 1H; 7.6, d, 1H; 3.98, s, 3H. 4.85 g (0.022 mol) of the above product are then added to a mixture of 5 ml of phosphorus oxychloride and 4.3 ml of ethyidiisopropylamine in 15 ml of 1,2dichloroethane, and the mixture is heated to a temperature of 60° C. After about 2 hours, another 2 ml of phosphorus oxychloride and 2.8 ml of ethyidiisopropylamine are added, and the mixture is stirred at this temperature for 20 hours. The reaction mixture is subsequently added to ice-water, adjusted to pH 3 using 30% NaOH and then extracted with dich ioromethane. Filtration through a little silica gel gives an approximately 5:1 product mixture of the two 6-chloro- and 2-chloro-4-trifluoromethylpyridin-3-yl methyl esters, which can be separated by HPLC into the pure components. Thus, pure methyl 6-chloro-4-trifluoromethylpyridin-3-ylcarboxylate is obtained as the main product;

1

H NMR (CDCl

3

, ppm): 8.91, s, 1H; 7.68, s, 1H; 3.98, s, 3H, and pure methyl 2-chloro-4-trifluoromethylpyridin-3-ylcarboxylate is obtained as the byproduct;

1

H NMR (CDCl

3

, ppm): 8.64, d, 1H; 7.52, d, 1H; 4.01, s, 3H. In the presence of 0.073 g of potassium hydroxide, 0.22 g of pure methyl 6-chloro-4-trifluoromethylpyridin-3-ylcarboxylate are hydrolysed at room temperature in a 1:1 mixture of 6 ml of dioxane/water. Recrystallization gives the pure 6-chloro-4-trifluoromethyinicotinic acid: m.p. 115-117° C.;

1

H NMR (CDCl

3

, ppm): 9.12, s, 1H; 7.24, s, 1H.

Example H4

Preparation of 6-methylthio-4-trifluoromethyinicotinic Acid

In boiling acetone, 0.70 g (2.9 mol) of methyl 6-chloro-4-trifluoromethylpyridin-3-ylcarboxylate is treated in the presence of a catalytic amount of 18-crown-6 with methanethiolate (0.33 g) until no further conversion can be detected by gas chromatographic analysis. The mixture is then filtered through silica gel and evaporated. This gives 0.73 g of methyl 6-methylthio-4-trifluoromethylpyridin-3-yicarboxylate;

1

H NMR (CDCl

3

, ppm): 8.98, s, 1H; 7.48, S, 1H; 3.94, s, 3H; 2.64, s, 3H. Hydrolysis under the conditions mentioned above gives 6-methylthio-4-trifluoromethylnicotinic acid:

1

H NMR (CDCl

3

, ppm): 9.02, s, 1H; 7.46, s, 1H; 2.64, s, 3H.

Example H5

6-Hydroxy-2-trifluoromethylpyridin-3-yl ethyl ester

Under an atmosphere of nitrogen and with stirring, 33.4 g of 3,4-dihydro-5-ethoxycarbonyl-6-trifluoromethylpyridin-2-one (Org. Res.& Devel. 1,370 (1997)) and 34 g of manganese dioxide in 250 ml of 1,2-dichlorobenzene are heated under reflux for 24 hours. In intervals of about 20 hours, manganese dioxide (total amount of MnO

2

used: 213 g) is added six more times over a period of 3 days, and the mixture is in each case heated further under ref lux. The mixture is then cooled, diluted with ethyl acetate, and filtered through silica gel, the filtercake is washed with ethyl ester and the filtrate is concentrated. The solid residue (26.7 g, i.e. 80%), which may still contain about 6% of starting material, is directly reacted further. For complete purification, it is possible to purify, for example, over silica gel (hexane/ethyl acetate 7:3) (

1

H NMR, CDCl

3

, ppm): 8.02 (d, 1H); 6.85 (d, 1H); 4.86 (q, 2H); 1.37 (t, 1H).

Example H6

Preparation of ethyl 6-chloro-2-trifluoromethyl pvridin-3-ylcarboxylate

In a bomb tube, 23.5 g of ethyl 6-hydroxy-2trifluoromethylpyridin-3-ylcarboxylate and 23.5 ml of phenyl dichlorophosphate are heated at 170° C. for 3 hours, and the mixture is, after cooling, added to ice-water, stirred for a few minutes and subsequently taken up in ethyl acetate and made slightly alkaline using sodium bicarbonate and then washed neutral with water. The extracts are admixed with a little hexane and filtered through silica gel. The filtrate is evaporated, leaving 21.6 g (85%) of the title compound in the form of a dark oil with n

D

30

, 1.4679.

1

H NMR (CDCl

3

, ppm): 8.09 (d,1H); 7.60 (d,1 H); 4.43 (q, 2H); 1.43 (t,3H).

Example H7

Preparation of 6-chloro-2-trifluoromethylpyridin-3-ylcarboxylic acid

2.5 g of the ethyl 6-chloro-2-trifluoromethylpyridin-3-ylcarboxylate obtained above are dissolved in the smallest possible amount of tetrahydrofuran, treated with approximately 20 g of ice and 11 ml of 1N lithium hydroxide and stirred at room temperature until hydrolysed completely. The mixture is then washed with a little ether and the aqueous phase is acidified using 4N hydrochloric acid and extracted with ethyl acetate. The extracts are washed with sodium chloride solution, dried and evaporated. This gives 1.8 g of the title compound of m.p. 154-156° C. The other free carboxylic acids are likewise obtained from their esters in this manner.

Example H8

Preparation of ethyl 6-methylthio-2-trifiuoromethylpyridin-3-ylcarboxylate

Under an atmosphere of nitrogen and with stirring, a solution of 1.7 g of 6-chloro-2-trifluoromethylpyridin-3-yl ethyl ester in 60 ml of dimethylformamide is treated a little at a time with 0.52 g of sodium methanethiolate and stirred at room temperature until the reaction has gone to completion. The reaction mixture is then poured into ice-water, made neutral by addition of a little dilute hydrochloric acid and extracted with ethyl acetate. The extracts are diluted with a little hexane, washed with water, dried over sodium sulfate, filtered and, after filtration through a little silica gel, evaporated. This gives 1.4 g (79%) of the title compound in the form of an oil with n

D

25

1.5100,

1

H NMR (CDCl

3

, ppm): 7.90 (d, 1H); 7.40 (d, 1H); 1.40 (q, 2H); 2.60 (s, 3H); 1.49 (t, 3H).

Example H9

Preparation of ethyl 6-ethylthio-2-trifluoromethylpyridin-3-ylcarboxylate

In an apparatus previously flushed with nitrogen, a solution of 1.8 ml of ethanethiol in 40 ml of dimethylformamide, which had been cooled to 0° C., is treated a little at a time with 0.96 g of sodium hydride oil dispersion (60%), and the mixture is stirred at room temperature. After evolution of hydrogen has ceased, the mixture is cooled to −20° C., and a solution of 5.07 g of 6-chloro-2-trifluoromethylpyridin-3-yl ethyl ester in 10 ml of dimethylformamide is added dropwise at this temperature, and the mixture is stirred slowly until room temperature has been reached. After the reaction has ended (approximately 3 hours), the reaction mixture is added to ice-water and extracted with ethyl acetate. The extracts are washed with water, dried, filtered, evaporated and dried under high vacuum. This gives 5.0 g (89%) of the title compound as a brownish oil.

1

H NMR (CDCl

3

, ppm): 7.90 (d, 1H); 7.35 (d, 1H); 4.40 (q, 2H); 3.25 (q, 2H); 1.38 (2t, 6H).

Example H10

Preparation of ethyl 6-ethylsulfinyl-2-trifluoromethylpyridin-3-ylcarboxylate

Under an atmosphere of nitrogen and with stirring and cooling, a solution of 2.5 g of m-chloroperbenzoic acid in 40 ml of methylene chloride is added dropwise at a temperature of −20° C. to a solution of 2.8 g of ethyl 6-ethylthio-2-trifluoromethylpyridin-3-ylcarboxylate, which had been charged initially, and the mixture is stirred at a temperature of +5° C. for 20 hours. The mixture is then evaporated gently and purified over silica gel (hexanelethyl acetate 7:3). This gives 2.48 g (84%) of 6-ethylsulfinyl-2-trifluoromethylpyridin-3-yl-ethyl ester.

1

H NMR (CDCl

3

, ppm): 8.38 (d, 1H); 8.30 (d, 1H); 4.45 (q, 2H); 3.26-3.00 (m, 2H); 1.43 (t, 3H); 1.26 (t, 3H).

Ethyl 6-methylsulfinyl-2-trifluoromethylpyridin-3-ylcarboxylate is obtained in an analogous manner.

Example H11

Preparation of ethyl 6-methylsulfonyl-2-trifluoromethylpyridin-3-ylcarboxylate

Under an atmosphere of nitrogen and with stirring and cooling, 21 g of m-chloroperbenzoic acid are introduced a little at a time over a period of 30 minutes at a temperature of −20° C. into a solution of 3.6 g of 6-methylthio-2-trifluoromethylpyridin-3-yl ethyl ester, which had been charged initially, and the reaction mixture is stirred at room temperature for 5 hours. The mixture is then evaporated and filtered through silica gel (ethyl acetate/methanol/triethylamine 85:10:5). This gives 3.95 g (97%) of ethyl 6-methylsulfonyl-2-trifluoromethylpyridin-3-ylcarboxylate as a brownish solid with m.p. 70-72° C.

1

H NMR (CDCl

3

, ppm): 8.40 (1H,d); 8.33 (1H,d); 4.47 (2H,q); 1.43 (3H,t).

Example H12

Preparation of ethyl 6-cyano-2-trifluoromethylpyridin-3-ylcarboxylate

Under an atmosphere of nitrogen and with stirring, a solution of 0.596 g of ethyl 6-methylsulfonyl-2-trifluoromethylpyridin-3-ylcarboxylate in 5 ml of dimethylformamide is treated with 160 mg of solid potassium cyanide and a spatula tipful of 18-crown-6, and the mixture is heated at 80° C. for 3 hours. The mixture is cooled overnight, and the next day another 30 mg of potassium cyanide are added and the mixture is heated further until the starting material has disappeared (approximately 2 hours). The mixture is then cooled, added to ice-water and extracted with ethyl acetate. The extracts are washed with water, dried, evaporated and freed from traces of dimethylformamide under high vacuum at approximately 40° C. This gives 480 mg (yield virtually quantitative) of ethyl 6-cyano-2-trifluoromethylpyridin-3-ylcarboxylate in the form of an oil which slowly solidifies.

1

H NMR (CDCl

3

, ppm): 8.29 (1H,d); 7.97 (1H,d); 4.48 (2H, d); 1.43 (3H,t).

Example H13

Preparation of ethyl 6-methyl-2-trifluoromethylpyridin-3-ylcarboxylate

Under an atmosphere of nitrogen and with stirring, a solution of 3.6 g of 6-chloro-2-trifluoromethylpyridin-3-yl ethyl ester in 20 ml of dimethylacetamide is treated with 4.5 ml of tetramethyltin and 200 mg of dichloro(bistriphenylphosphine)palladium, and the mixture is heated to a temperature of 80-90° C. for 24 hours. Then another 1.5 ml of tetramethyltin and 30 mg of dichloro(bistriphenylphosphine)palladium are added and the mixture is heated for another 6 hours. The reaction mixture is then freed from excess tetramethyltin using reduced pressure (destruction by passing through ethanolic sodium hydroxide solution), cooled and added to ice-water. The mixture is extracted with diethyl ether and the extract is washed with water, dried over sodium sulfate, filtered through a little silica gel, evaporated and dried under reduced pressure. This gives the title compound (2.4 g, 73%), which still contains traces of dimethylacetamide, in the form of a dark oil.

1

H NMR (CDCl

3

, ppm): 8.00 (1H,d); 7.42 (1H,d); 4.42 (2H, d); 2.68 (3H, s); 1.41 (3H,t). Hydrolysis analogously to the description already mentioned above affords 6-methyl-2-trifluoromethylpyridin-3-ylcarboxylic acid (brown resin) which is directly converted further into the carbonyl chloride.

Example H14

Preparation of 6-methyl-2-trifluoromethyl pvridin-3-ylcarbonyl chloride

A solution of 0.45 g of 6-methyl-2-trifluoromethylpyridin-3-ylcarboxyi ic acid in 20 ml of dichloromethane is charged initially, 3 drops of dimethylformamid c are added and the mixture is subsequently treated with 1.6 ml of oxalyl chloride. After the intensive evolution of gas has ceased, the mixture is kept at a bath temperature of 40° C. for another 1.5 hours and then evaporated. The crude product (0.56 g) that remains as residue can be directly reacted further.

1

H NMR (CDCl

3

, ppm): 8.20 (1H,d); 7.51 (1H,d); 2.65 (3H, s).

Example H15

Preparation of 4-oxobicyclo[3.2.1]oct-2-en-2-yl 6-methyl-2- trifluoromethylnicotinate

Under an atmosphere of nitrogen and with stirring and cooling, a solution of 0.56 g of 6-methyl-2-trifluoromethylpyridin-3-ylcarbonyl chloride in 10 ml of methylene chloride is added dropwise at 0° C. to a solution of 0.4 g of bicyclo[3.2.1]octane-2,4-dione and 0.72 g of triethylamine in 10 ml of methylene chloride, and the mixture is stirred for 5 hours until room temperature has been reached. The mixture is then diluted with methylene chloride, washed with cold 1N hydrochloric acid, dried and evaporated to give the desired enol ester (0.8 g) as a brown resin which is directly reacted further.

1

H NMR (CDCl

3

, ppm): 8.17 (1H,d); 7.51 (1H, d); 5.96 (1H, s); 3.04 (2H, m); 2.75 (3H, s);2.32-1.30 (m).

Example H16

Preparation of 4-hydroxy-3-(6-methyl-2-trifluoromethylpyridin-3-carbonyl)-bicyclo[3.2.1]oct-3-en-2-one

Under an atmosphere of nitrogen and with stirring, 0.8 g of the above enol ester is dissolved in 30 ml of acetonitrile at 25° C., and the mixture is treated with 0.5 ml of triethylamine and 0.4 ml of acetone cyanohydrin and stirred at room temperature for 20 hours. The mixture is then diluted with solvent and washed with dilute hydrochloric acid, dried and evaporated, and the residue is purified through a little silica gel (ethyl acetate/methanol/triethylamine 85:10:5). This gives 371 mg (46%) of the title compound (triethylamine salt) in the form of a yellowish resin.

1

H NMR (CDCl

3

, ppm): 7.45 (1H, d); 7.25 (1H, d); 3.80-3.43 (4H, m); 3.18 (6H, m); 2.80 (2H, s(br)); 2.62 (3H, s); 220-1.54 (m).

Example H17

Preparation of ethyl 6-methoxy-2-trifluoromethylpyridin-3-ylcarboxylate

A suspension of 5.65 g of ethyl 6-hydroxy-2-trifluoromethylpyridin-3-ylcarboxylate, 6.0 g of potassium carbonate and 2.7 ml of methyl iodide is, together with a spatula tipful of 18-crown-6, heated to a temperature of 60-70° C. until the reaction has gone to completion. The mixture is then filtered, the filtration residue is washed with acetonitrile and the filtrate is concentrated under reduced pressure. The residue is cooled, admixed with ice-water, neutralized with dilute sulfuric acid and extracted with ethyl acetate. The extracts are washed with water, dried, diluted with a little hexane and filtered through a little silica gel.

The resulting residue is the title compound (3.7 g, 65%) in the form of slightly orange crystals of m.p. 150-152° C.

1

H NMR (CDCl

3

, ppm): 8.00 (1H, d); 6.83 (1H, d); 4.38 (2H, q); 4.01 (3H, s);1.39 (3H, t).

Example H18

Preparation of 4-hydroxy-3(2-methyl-6-trifluoromethylpyridin-3-carbonyl)-bicyclo[3.2.1]oct-3-en-2-one

6.68 g (0.0305 mol) of methyl 2-methyl-6-trifluoromethyinicotinate (prepared as described in Heterocycles, 46, 129 (1997)) are dissolved in 250 ml of methanovwater (3:1 mixture), and 1.92 g (0.046 mol) of lithium hydroxide hydrate are added a little at a time at 22° C. After 4 hours at 22° C, the reaction mixture is poured into ethyl acetate and 2N hydrochloric acid, the organic phase is washed three times with water, dried with sodium sulfate and evaporated and the residue is triturated with a little hexane. Filtration gives 5.69 g (90% of theory) of the expected 2-methyl-6-trifluoromethyinicotinic acid of m.p. 147-149° C. The 2-methyl6trifluoromethyinicotinic acid obtained (2.0 g, 0.0098 mol) is dissolved in 20 ml of oxalyl chloride. Three drops of dimethylformamide are added, and the mixture is heated under reflux for 1 hour. The mixture is then concentrated using a rotary evaporator, and the residue (2-methyl-6-trifluoromethyinicotinoyl chloride) is taken up in 30 ml of methylene chloride. At 0° C., 2.7 ml (0.0196 mol) of triethylamine and 0.12 g (0.00098 mol) of dimethylaminopyridine are added. 1.49 g (0.0108 mol) of bicyclo[3.2.1]octane-2,4-dione, dissolved in 20 ml of methylene chloride, are then added dropwise. After 3 hours at 22° C., the reaction mixture is extracted with 2 N hydrochloric acid. The methylene chloride phase is separated off, washed with water and subsequently extracted with 10% aqueous sodium bicarbonate solution, dried over sodium sulfate and evaporated. This gives 3.18 g (100% of theory) of 4-oxobicyclo[3.2.1]oct-2-en-2-yl 2-methyl-6-trifluoromethyinicotinate as an oil, which can be processed further without purification.

3.02 g (0.0093 mol) of 4-oxobicyclo [3.2.1]oct-2en-2-yl 2-methyl-6-trifluoromethyinicotinate and 1.9 ml (0.0136 mo l) of triethylamine are dissolved in 45 ml of acetonitrile. At 22° C., 0.01 ml of acetone cyanohydrin are added. After 18 hours at 22° C., the reaction mixture is poured into dilute hydrochloric acid and extracted with ethyl acetate. The ethyl acetate phase is washed with water and then with brine, dried over sodium sulfate and evaporated, and the residue is dissolved in a little warm acetone. The product crystallizes on standing. Filtration gives 0.99 g (33% of theory) of the expected 4-hydroxy-3-(2-methyl-6-trifluoromethylpyridine-3-carbonyl)bicyclo[3.2.1]oct-3-en-2-one as white crystals (m.p. 75-77° C.).

Example H19

Preparation of 3-(2-methyl-6-trifluoromethylpyridine-3-carbonyl)-4-oxo-bicyclo[3.2.1]oct-2-en-2-yl benzoate

At 0° C., a solution of 0.562 g (0.0004 mol) of benzoyl chloride in 1 ml of tetrahydrofuran is added to a solution of 1.14 g (0.0035 mol) of 4-hydroxy-3-(2-methyl-6-trifluoromethylpyridine-3-carbonyl)bicyclo[3.2.1]oct-3-en-2-one and 0.517 g (0.004 mol) of ethyidiisopropylamine in 15 ml of tetrahydrofuran. The reaction mixture is stirred at 25° C. for 2 hours, evaporated and purified over silica gel (hexane/ethyl acetate 1:1). This gives 0.9 g (60%) of the title compound in the form of a yellowish resin.

1

H NMR (CDCl

3

, ppm): 7.91-7.87, m, 3H; 7.64, t, J=7.5 Hz, 1 H; 7.5 0-7.40, m, 3H; 3.24, br t, J=4 Hz, 1 H; 3.14, br t, J=4 Hz, 1H; 2.70, s, 3H; 2.47, d, J=13.5 Hz, 1H; 2.40, 2.15, m, 3H; 1.95-1.8, m, 2H.

Example H20

Preparation of 4-hydroxy-3-(2-methyl-1-oxy-6-trifluoromethylpyridine-3-carbonyl)bicyclo[3.2.1]oct-3-en-2-one

16.25 g (0.05 mol) of 4-hydroxy-3-(2-methyl-6-trifluoromethylpyridine-3-carbonyl)-bicyclo[3.2.1]oct-3-en-2-one and 9.4 g (0.1 mol) of urea/hydrogen peroxide complex are dissolved in 150 ml of methylene chloride, and 20.5 ml (0.15 mol) of trifluoroacetic anhydride are added dropwise at 25° C. After 14 hours at 25° C., the reaction mixture is added to ethyl acetate and water, and the organic phase is washed twice with water, dried with sodium sulfate and evaporated. The residue is chromatographed over silica gel (mobile phase: ethyl acetatelmethanol 9/1). This gives 6.8 g (40%) of the desired product as white crystals (m.p. 109-110° C.).

Example H21

Preparation of 4-chloro-3-(2-methyl-6-trifluoromethylpyridine-3-carbonyl)-bicyclo[3.2.1]oct-3-en-2-one

20.15 g (0.062 mo l) of 4-hydroxy-3-(2-methyl-6-trifluoromethyipyridine-3carbonyl)-bicyclo[3.2.1]oct-3-en-2-one are suspended in 50 ml of oxalyl chloride, and 0.1 ml of dimethylformamide are added dropwise. After the intensive evolution of gas has ceased, the mixture is kept at a bath temperature of 45° C. for another 1.5 hours and then evaporated, and the residue is suspended in a little ethyl acetate and admixed with stirring at 0° C. with hexane. Filtration gives 19.19 g (90% of theory) of 4-chloro-3-(2-methyl-6-trifluoromethyl-pyridine-3-carbonyl)bicyclo[3.2.1]oct-3-en-2-one of m.p. 137-138° C.

Example H22

Preparation of 4-amino-3-(2-methyl-6-trifluoronmethvlpvridine-3-carbonyl)-bicyclo[3.2.1]oct-3-en-2one

1.0 g (0.0029 mol) of 4-chloro-3-(2-methyl-6-trifluoromethylpyridine-3-carbonyl)-bicyclo[3.2.1]oct-3-en-2-one are dissolved in 10 ml of tetrahydrofuran and, at 25° C., treated with 2.0 ml of aqueous ammonia (30%). After 0.5 hours at 25° C., the reaction mixture is added to ethyl acetate and water, the organic phase is washed twice with water, dried with sodium sulfate and evaporated and the residue is triturated with a little ethyl acetate. Filtration gives 0.81 g (86% of theory) of 4-amino-3-(2-methyl-6-trifluoromethylpyridine-3-carbonyl)bicyclo[3.2.1]oct-3en-2-one in the form of white crystals (m.p. 262-263° C).

1

H NMR (CDCl

3

, ppm): 10.62 br s 1H; 8.223 br s 1H; 7.41, d, J=8.1 Hz, 1H; 7.35, d, J=8.1 Hz, 1H; 3.03, br t, J=4.8 Hz, 1H; 2.70, br t, J=4.8 Hz, 1H; 2.41, s, 3H; 1.97-2.14, m, 3H; 1.77-1.812, m, 1H; 1.47-1.70, m, 2H.

Example H23

Preparation of 4-(4-chlorophenylsulfanyl)-3-(2-methyl-6-trifluoromethyl-pyridine-3-carbonyl)bicyclo[3.2.1]oct-3-en-2-one

2.0 g (0.0058 mol) of 4-chloro-3-(2-methyl-6-trifluoromethylpyridine-3-carbonyl)-bicyclo[3.2.1]oct-3-en-2-one, 0.07 g of dimethylaminopyridine (0.00058 mol) and 1.61 ml of triethylamine are dissolved in 15 ml of methylene chloride. At 25° C., 0.092 g (0.0064 mol) of 4-chlorothiophenol are added. After 2 hours at 22° C., the reaction mixture is evaporated and purified over silica gel (hexane/ethyl acetate 2:1). Recrystallization (hexane/acetic acid at −25° C.) gives pure 4-(4-chlorophenylsulfanyl)-3-(2-methyl-6-trifluoromethylpyridine-3-carbonyl)bicyclo[3.2.1]oct-3-en-2-one: m.p. 130-131 ° C.

Example H24

Preparation of 4-(4-chlorobenzenesulfonyl)-3-(2-methyl-6-trifluoromethyl-pyridine-3-carbonyl)bicyclo[3.2.1]oct-3-en-2-one

0.6 g (0.00133 mol) of the 4-(4-chlorophenylsul tanyl)-3-(2-methyl-6trifluoromethylpyridine-3-carbonyl)bicyclo[3.2.1]oct-3-en-2-one obtained above is dissolved in methylene chloride, and 0.9 ml of peracetic acid (39% in acetic acid, 0.0053 mol) are added dropwise at 25° C. After 5 hours at 25° C., the reaction mixture is added to ethyl acetate and water, the organic phase is washed with water, dried with sodium sulfate and evaporated and the residue is triturated with a little hexane. Filtration gives 0.56 g (84% of theory) of 4-(4-chlorobenzenesulfonyl)-3-(2-methyl-6-trifluoromethylpyridine-3-carbonyl)bicyclo[3.2.1]oct-3-en-2-one in the form of white crystals (m.p.166-167° C.).

Example H25

Preparation of (5-cyclopropyl-3-methylsulfanylisoxazol-4-yl)-(2-methyl-6-trifluoromethylpyridin-3-yl)methanone and cyclopropyl-[3-methylsulfanyl-5-(2-methyl-6-trifluoromethylpyridin-3-yl)isoxazol4-yl)methanone

14.8 g (0.080 mol) of tert-butyl 3-cyclopropyl-3-oxopropionic acid ester are dissolved in 25 ml of MeOH, and 1.93 g (0 .080 mol) of magnesium are added. With ice-bath cooling, 7 ml of carbon tetrachloride are added dropwise, and the reaction mixture is stirred at a temperature of 22° C. for one hour. After evaporation, the residue is suspended in 100 ml of acetonitrile, and 16.31 g (0.073 mol) of 2-methyl-6-trifluoromethyinicotinoyl chloride (prepared as described in Example H18), dissolved in 50 ml of acetonitrile, are added dropwise at a temperature of 22° C. After 6 hours, the reaction mixture is taken up in ethyl acetate and washed with saturated sodium bicarbonate solution. The ethyl acetate phase is separated off, washed with water, dried over sodium sulfate and evaporated. The residue is dissolved in 160 ml of methylene chloride, and 10 ml of trifluoroacetic acid are added dropwise at a temperature of 22° C. After 18 hours, the reaction mixture is poured into water and extracted with methylene chloride. The methylene chloride phase is washed with water and then with saturated aqueous sodium chloride solution, dried over sodium sulfate and evaporated. This gives 17.3 g (88% of theory) of 1-cyclopropyl-3-(2-methyl-6-trifluoromethylpyridin-3-yl)propane-1,3-dione as an oil, which is processed further without purification. The 1-cyclopropyl-3-(2-methyl-6-trifluoromethylpyridin-3-yl)propane-1,3-dione obtained above (15.0 g, 0.055 mol) is dissolved in 150 ml of dimethylformamide, and 50 g of potassium fluoride on an aluminium oxide support (alumina) (0.0055 movg, 0.276 mol) are added a little at a time at a temperature of 0° C. After 5 minutes, 6.7 g (0.088 mol) of carbon disulfide are added dropwise. After 2 hours, 23.6 g (0.166 mol) of methyl iodide are added dropwise, and the reaction mixture is warmed to a temperature of 22° C. After a further 2 hours, the alumina is filtered off, the filtrate is added to water and the mixture is extracted with ethyl acetate. The ethyl acetate phase is washed with water and then with saturated aqueous sodium chloride solution, dried over sodium sulfate and evaporated. The residue is chromatographed over silica gel (mobile phase: ethyl acetate/hexane 15/1). This gives 12.0 g (60% of theory) of 2-(bismethylsulfanylmethylene)-1-cyclopropyl-3-(2-methyl-6-trifluoromethylpyridin-3-yl)-propane-1,3-dione as a solid. 12.0 g (0.033 mol) of the product obtained above are, together with 5.4 g (0.066 mol) of anhydrous sodium acetate, suspended in 120 ml of ethanol. 4.6 g (0.066 mol) of hydroxylamine hydrochloride are added, and the reaction mixture is kept at a temperature of 22° C. for 5 hours. Another 2.7 g of anhydrous sodium acetate and 2.3 g of hydroxylamine hydrochloride are then added. After 18 hours, the reaction mixture is diluted with water and extracted with ethyl acetate. The ethyl acetate phase is washed with water and then with saturated aqueous sodium chloride solution, dried over sodium sulfate and evaporated. Trituration with a little ethyl acetate gives 9.0 g (79.5%) of the desired product as a 2:1 isomer mixture in the form of white crystals (m.p. 103-104° C.).

Main isomer:

1

H NMR (CDCl

3

, ppm) ((5-cyclopropyl-3-methylsulfanylisoxazol-4-yl)-(2-methyl-6-trifluoromethylpyridin-3-yl)methanone) 7.98, d, J=7.8 Hz, 1H; 7.61, d, J=7.8 Hz, 1H; 2.67, s, 3H; 2.50, s, 3H; 2.02-1.93, m, 1 H; 1.34-1.28, m, 2H; 1.18-1.09, m, 2H.

1

H NMR (CDCl

3

, ppm) (cyclopropyl-13-methylsulfanyl-5-(2-methyl6-trifluoromethylpyridin-3-yl)isoxazol-4-yl]methane): 7.95, d, J=7.8 Hz, 1H; 7.69, d, J=7.8 Hz, 1H; 2.67, s, 3H; 2.66, s, 3H; 1.74-1.64, m, 1H; 1.28-1.18, m, 2H; 0.89 4.80, m, 2H.

Example H26

Preparation of (5-cyclopropyl-3-methylsulfinylisoxazol-4-yl)-(2-methyl-6-trifluoromethylpyridin-3-yl)methanone and cylopropyl-[3-methanesulfinyl-5-(2-methyl-6-trifluoromethylpyridin-3-yl)isoxazol-4-yl]methanone

1.50 g (0.0043 mol) of the isomer mixture obtained above are dissolved in 30 ml of acetonelwater (2:1 mixture), and 1.02 g (0.0048 mol) of sodium metaperiodate are added a little at a time at 22° C. After 5 hours, the reaction mixture is evaporated using a rotary evaporator. The residue is taken up in water and ethyl acetate. The ethyl acetate phase is dried over sodium sulfate and evaporated. The residue is chromatographed over silica gel (mobile phase: ethyl acetate/hexane 3/1). This gives initially 0.8 g (51% of theory) of (5-cyclopropyl-3-methylsulfinylisoxazol-4-yl)-(2-methyl-6-trifluoromethylpyridin-3-yl)methanone as white crystals (m.p. 96-97° C.).

1

H NMR (CDCl

3

, ppm): 7.86, d, J=7.8 Hz, 1H; 7.59, d, J=7.8 Hz, 1H; 3.078, s, 3H; 2.66, s, 3H; 1.54-1A49, m, IH; 1.32-1.25, m, 2H; 1.13-1.072, m, 2H.

The second product that eiutes consists of 0.34 g (22% of theory) of cyclopropyl-[3-methanesulfinyl-5-(2-methyl-6-trifluoromethylpyridin-3yl)isoxazol4-yl]methanone as white crystals (m.p. 112-113° C.).

1

H NMR (CDCl

3

, ppm): 7.97, d, J=7.8 Hz, 1H; 7.67, d, J=7.8 Hz, 1H; 3.128, s, 3H; 2.62, s, 3H; 1.69-1.64, m, 1H; 1.26-1.18, m, 2H; 0.90-0.85, m, 2H.

Example H27

Preparation of (5-cyclopropyl-3-methanesulfonylisoxazol-4-yl)-(2-isopropyl-6-trifluoromethylpyridin-3-yl)methanone

0.15 g (0.0045 mol) of (5-cyclopropyl-3-methylsulfanylisoxazol-4-yl)-(2-isopropyl-6-trifluoromethylpyridin-3-yl)methanone is dissolved in methylene chloride, and 0.28 ml of peracetic acid (39% in acetic acid, 0.0016 mol) are added dropwise at a temperature of 5° C. After 15 hours at 25° C., the reaction mixture is added to ethyl acetate and water, and the organic phase is washed with water, dried with sodium sulfate and evaporated. The residue is chromatographed over silica gel (mobile phase: ethyl acetate/hexane 5/1). This gives 0.121 g (74% of theory) of the expected product as white crystals (m.p.105-106° C.).

In an analogous manner, and according to the methods shown in the general reaction schemes 1-10 and in the references mentioned therein, it is also possible to prepare the compounds listed in the tables below. In these tables, CCH is the ethynyl group, Ph is the phenyl group and Me is the methyl group.

TABLE 1

Comp.

No.

R

1

R

2

R

3

R

4

R

5

p

1.001

H

CF

3

H

H

OH

0

1.002

F

CF

3

H

H

OH

0

1.003

Cl

CF

3

H

H

OH

0

1.004

Br

CF

3

H

H

OH

0

1.005

CHF

2

CF

3

H

H

OH

0

1.006

CCl

3

CF

3

H

H

OH

0

1.007

CClF

2

CF

3

H

H

OH

0

1.008

CF

3

CF

3

H

H

OH

0

1.009

CH

3

CF

3

H

H

OH

0

1.01

CH

2

CH

3

CF

3

H

H

OH

0

1.011

CH(CH

3

)

2

CF

3

H

H

OH

0

1.012

(CH

2

)

2

CH

3

CF

3

H

H

OH

0

1.013

C(CH

3

)

3

CF

3

H

H

OH

0

1.014

Ph

CF

3

H

H

OH

0

1.015

CH

2

F

CF

3

H

H

OH

0

1.016

CH

2

Cl

CF

3

H

H

OH

0

1.017

CH

2

Br

CF

3

H

H

OH

0

1.018

CH

2

OH

CF

3

H

H

OH

0

1.019

CH

2

OCOCH

3

CF

3

H

H

OH

0

1.02

CH

2

OCOPh

CF

3

H

H

OH

0

1.021

CH

2

OCH

3

CF

3

H

H

OH

0

1.022

CH

2

OCH

2

CH

3

CF

3

H

H

OH

0

1.023

CH

2

CH

2

OCH

3

CF

3

H

H

OH

0

1.024

CH

2

SMe

CF

3

H

H

OH

0

1.025

CH

2

SOMe

CF

3

H

H

OH

0

1.026

CH

2

SO

2

Me

CF

3

H

H

OH

0

1.027

CH

2

SO

2

Ph

CF

3

H

H

OH

0

1.028

SCH

2

Ph

CF

3

H

H

OH

0

1.029

SOCH

2

Ph

CF

3

H

H

OH

0

1.03

SO

2

CH

2

Ph

CF

3

H

H

OH

0

1.031

SCH

3

CF

3

H

H

OH

0

1.032

SOCH

3

CF

3

H

H

OH

0

1.033

SO

2

CH

3

CF

3

H

H

OH

0

1.034

SPh

CF

3

H

H

OH

0

1.035

SOPh

CF

3

H

H

OH

0

1.036

SO

2

Ph

CF

3

H

H

OH

0

1.037

N(CH

3

)

2

CF

3

H

H

OH

0

1.038

CH═CH

2

CF

3

H

H

OH

0

1.039

CH

2

CH═CH

2

CF

3

H

H

OH

0

1.04

SO

2

N(CH

3

)

2

CF

3

H

H

OH

0

1.041

ethynyl

CF

3

H

H

OH

0

1.042

cyclopropyl

CF

3

H

H

OH

0

1.043

OCH

3

CF

3

H

H

OH

0

1.044

OPh

CF

3

H

H

OH

0

1.045

OCHF

2

CF

3

H

H

OH

0

1.046

CO

2

Me

CF

3

H

H

OH

0

1.047

2-furyl

CF

3

H

H

OH

0

1.048

OCH

2

ethynyl

CF

3

H

H

OH

0

1.049

2-pyridyl

CF

3

H

H

OH

0

1.05

3-pyridyl

CF

3

H

H

OH

0

1.051

4-pyridyl

CF

3

H

H

OH

0

1.052

H

CF

3

H

H

OH

1

1.053

F

CF

3

H

H

OH

1

1.054

Cl

CF

3

H

H

OH

1

1.055

Br

CF

3

H

H

OH

1

1.056

CHF

2

CF

3

H

H

OH

1

1.057

CCl

3

CF

3

H

H

OH

1

1.058

CClF

2

CF

3

H

H

OH

1

1.059

CF

3

CF

3

H

H

OH

1

1.06

CH

3

CF

3

H

H

OH

1

1.061

CH

2

CH

3

CF

3

H

H

OH

1

1.062

CH(CH

3

)

2

CF

3

H

H

OH

1

1.063

(CH

2

)

2

CH

3

CF

3

H

H

OH

1

1.064

C(CH

3

)

3

CF

3

H

H

OH

1

1.065

Ph

CF

3

H

H

OH

1

1.066

CH

2

F

CF

3

H

H

OH

1

1.067

CH

2

Cl

CF

3

H

H

OH

1

1.068

CH

2

Br

CF

3

H

H

OH

1

1.069

CH

2

OH

CF

3

H

H

OH

1

1.07

CH

2

OCOCH

3

CF

3

H

H

OH

1

1.071

CH

2

OCOPh

CF

3

H

H

OH

1

1.072

CH

2

OCH

3

CF

3

H

H

OH

1

1.073

CH

2

OCH

2

CH

3

CF

3

H

H

OH

1

1.074

CH

2

CH

2

OCH

3

CF

3

H

H

OH

1

1.075

CH

2

SMe

CF

3

H

H

OH

1

1.076

CH

2

SOMe

CF

3

H

H

OH

1

1.077

CH

2

SO

2

Me

CF

3

H

H

OH

1

1.078

CH

2

SO

2

Ph

CF

3

H

H

OH

1

1.079

SCH

2

Ph

CF

3

H

H

OH

1

1.08

SOCH

2

Ph

CF

3

H

H

OH

1

1.081

SO

2

CH

2

Ph

CF

3

H

H

OH

1

1.082

SCH

3

CF

3

H

H

OH

1

1.083

SOCH

3

CF

3

H

H

OH

1

1.084

SO

2

CH

3

CF

3

H

H

OH

1

1.085

SPh

CF

3

H

H

OH

1

1.086

SOPh

CF

3

H

H

OH

1

1.087

SO

2

Ph

CF

3

H

H

OH

1

1.088

N(CH

3

)

2

CF

3

H

H

OH

1

1.089

CH═CH

2

CF

3

H

H

OH

1

1.09

CH

2

CH═CH

2

CF

3

H

H

OH

1

1.091

SO

2

N(CH

3

)

2

CF

3

H

H

OH

1

1.092

ethynyl

CF

3

H

H

OH

1

1.093

cyclopropyl

CF

3

H

H

OH

1

1.094

OCH

3

CF

3

H

H

OH

1

1.095

OPh

CF

3

H

H

OH

1

1.096

OCHF

2

CF

3

H

H

OH

1

1.097

CO

2

Me

CF

3

H

H

OH

1

1.098

2-furyl

CF

3

H

H

OH

1

1.099

OCH

2

CCH

CF

3

H

H

OH

1

1.1

2-pyridyl

CF

3

H

H

OH

1

1.101

3-pyridyl

CF

3

H

H

OH

1

1.102

4-pyridyl

CF

3

H

H

OH

1

1.103

H

CF

2

CF

3

H

H

OH

0

1.104

Cl

CF

2

CF

3

H

H

OH

0

1.105

CHF

2

CF

2

CF

3

H

H

OH

0

1.106

CCl

3

CF

2

CF

3

H

H

OH

0

1.107

CClF

2

CF

2

CF

3

H

H

OH

0

1.108

CF

3

CF

2

CF

3

H

H

OH

0

1.109

CH

3

CF

2

CF

3

H

H

OH

0

1.11

CH

2

CH

3

CF

2

CF

3

H

H

OH

0

1.111

CH(CH

3

)

2

CF

2

CF

3

H

H

OH

0

1.112

(CH

2

)

2

CH

3

CF

2

CF

3

H

H

OH

0

1.113

C(CH

3

)

3

CF

2

CF

3

H

H

OH

0

1.114

CH

2

F

CF

2

CF

3

H

H

OH

0

1.115

CH

2

Cl

CF

2

CF

3

H

H

OH

0

1.116

CH

2

OH

CF

2

CF

3

H

H

OH

0

1.117

CH

2

OCOCH

3

CF

2

CF

3

H

H

OH

0

1.118

CH

2

OCOPh

CF

2

CF

3

H

H

OH

0

1.119

CH

2

OCH

3

CF

2

CF

3

H

H

OH

0

1.12

CH

2

OCH

2

CH

3

CF

2

CF

3

H

H

OH

0

1.121

CH

2

SMe

CF

2

CF

3

H

H

OH

0

1.122

CH

2

SOMe

CF

2

CF

3

H

H

OH

0

1.123

CH

2

SO

2

Me

CF

2

CF

3

H

H

OH

0

1.124

CH

2

SO

2

Ph

CF

2

CF

3

H

H

OH

0

1.125

N(CH

3

)

2

CF

2

CF

3

H

H

OH

0

1.126

CH═CH

2

CF

2

CF

3

H

H

OH

0

1.127

CH

2

CH═CH

2

CF

2

CF

3

H

H

OH

0

1.128

SO

2

N(CH

3

)

2

CF

2

CF

3

H

H

OH

0

1.129

CCH

CF

2

CF

3

H

H

OH

0

1.13

cyclopropyl

CF

2

CF

3

H

H

OH

0

1.131

OPh

CF

2

CF

3

H

H

OH

0

1.132

OCH

3

CF

2

CF

3

H

H

OH

0

1.133

CO

2

Me

CF

2

CF

3

H

H

OH

0

1.134

OCH

2

CCH

CF

2

CF

3

H

H

OH

0

1.135

2-pyridyl

CF

2

CF

3

H

H

OH

0

1.136

3-pyridyl

CF

2

CF

3

H

H

OH

0

1.137

4-pyridyl

CF

2

CF

3

H

H

OH

0

1.138

H

CF

2

CF

3

H

H

OH

1

1.139

Cl

CF

2

CF

3

H

H

OH

1

1.14

CHF

2

CF

2

CF

3

H

H

OH

1

1.141

CCl

3

CF

2

CF

3

H

H

OH

1

1.142

CClF

2

CF

2

CF

3

H

H

OH

1

1.143

CF

3

CF

2

CF

3

H

H

OH

1

1.144

CH

3

CF

2

CF

3

H

H

OH

1

1.145

CH

2

CH

3

CF

2

CF

3

H

H

OH

1

1.146

CH(CH

3

)

2

CF

2

CF

3

H

H

OH

1

1.147

(CH

2

)

2

CH

3

CF

2

CF

3

H

H

OH

1

1.148

C(CH

3

)

3

CF

2

CF

3

H

H

OH

1

1.149

CH

2

F

CF

2

CF

3

H

H

OH

1

1.15

CH

2

Cl

CF

2

CF

3

H

H

OH

1

1.151

CH

2

OH

CF

2

CF

3

H

H

OH

1

1.152

CH

2

OCOCH

3

CF

2

CF

3

H

H

OH

1

1.153

CH

2

OCOPh

CF

2

CF

3

H

H

OH

1

1.154

CH

2

OCH

3

CF

2

CF

3

H

H

OH

1

1.155

CH

2

OCH

2

CH

3

CF

2

CF

3

H

H

OH

1

1.156

CH

2

SMe

CF

2

CF

3

H

H

OH

1

1.157

CH

2

SOMe

CF

2

CF

3

H

H

OH

1

1.158

CH

2

SO

2

Me

CF

2

CF

3

H

H

OH

1

1.159

CH

2

SO

2

Ph

CF

2

CF

3

H

H

OH

1

1.16

N(CH

3

)

2

CF

2

CF

3

H

H

OH

1

1.161

CH═CH

2

CF

2

CF

3

H

H

OH

1

1.162

CH

2

CH═CH

2

CF

2

CF

3

H

H

OH

1

1.163

SO

2

N(CH

3

)

2

CF

2

CF

3

H

H

OH

1

1.164

CCH

CF

2

CF

3

H

H

OH

1

1.165

cyclopropyl

CF

2

CF

3

H

H

OH

1

1.166

OPh

CF

2

CF

3

H

H

OH

1

1.167

OCH

3

CF

2

CF

3

H

H

OH

1

1.168

CO

2

Me

CF

2

CF

3

H

H

OH

1

1.169

OCH

2

CCH

CF

2

CF

3

H

H

OH

1

1.17

2-pyridyl

CF

2

CF

3

H

H

OH

1

1.171

3-pyridyl

CF

2

CF

3

H

H

OH

1

1.172

4-pyridyl

CF

2

CF

3

H

H

OH

1

1.173

H

CF

2

CF

2

CF

3

H

H

OH

0

1.174

CHF

2

CF

2

CF

2

CF

3

H

H

OH

0

1.175

CF

3

CF

2

CF

2

CF

3

H

H

OH

0

1.176

CH

3

CF

2

CF

2

CF

3

H

H

OH

0

1.177

CH

2

CH

3

CF

2

CF

2

CF

3

H

H

OH

0

1.178

(CH

2

)

2

CH

3

CF

2

CF

2

CF

3

H

H

OH

0

1.179

CH

2

Cl

CF

2

CF

2

CF

3

H

H

OH

0

1.18

CH

2

OCH

3

CF

2

CF

2

CF

3

H

H

OH

0

1.181

H

CF

2

CF

2

CF

3

H

H

OH

1

1.182

CHF

2

CF

2

CF

2

CF

3

H

H

OH

1

1.183

CF

3

CF

2

CF

2

CF

3

H

H

OH

1

1.184

CH

3

CF

2

CF

2

CF

3

H

H

OH

1

1.185

CH

2

CH

3

CF

2

CF

2

CF

3

H

H

OH

1

1.186

(CH

2

)

2

CH

3

CF

2

CF

2

CF

3

H

H

OH

0

1.187

CH

2

Cl

CF

2

CF

2

CF

3

H

H

OH

1

1.188

CH

2

OCH

3

CF

2

CF

2

CF

3

H

H

OH

1

1.189

H

CF

2

Cl

H

H

OH

0

1.19

Cl

CF

2

Cl

H

H

OH

0

1.191

CHF

2

CF

2

Cl

H

H

OH

0

1.192

CCl

3

CF

2

Cl

H

H

OH

0

1.193

CClF

2

CF

2

Cl

H

H

OH

0

1.194

CF

3

CF

2

Cl

H

H

OH

0

1.195

CH

3

CF

2

Cl

H

H

OH

0

1.196

CH

2

CH

3

CF

2

Cl

H

H

OH

0

1.197

CH(CH

3

)

2

CF

2

Cl

H

H

OH

0

1.198

(CH

2

)

2

CH

3

CF

2

Cl

H

H

OH

0

1.199

C(CH

3)

3

CF

2

Cl

H

H

OH

0

1.2

CH

2

F

CF

2

Cl

H

H

OH

0

1.201

CH

2

Cl

CF

2

Cl

H

H

OH

0

1.202

CH

2

OH

CF

2

Cl

H

H

OH

0

1.203

CH

2

OCOCH

3

CF

2

Cl

H

H

OH

0

1.204

CH

2

OCOPh

CF

2

Cl

H

H

OH

0

1.205

CH

2

OCH

3

CF

2

Cl

H

H

OH

0

1.206

CH

2

OCH

2

CH

3

CF

2

Cl

H

H

OH

0

1.207

CH

2

SMe

CF

2

Cl

H

H

OH

0

1.208

CH

2

SOMe

CF

2

Cl

H

H

OH

0

1.209

CH

2

SO

2

Me

CF

2

Cl

H

H

OH

0

1.21

CH

2

SO

2

Ph

CF

2

C

H

H

OH

0

1.211

N(CH

3

)

2

CF

2

Cl

H

H

OH

0

1.212

CH═CH

2

CF

2

Cl

H

H

OH

0

1.213

CH

2

CH═CH

2

CF

2

Cl

H

H

OH

0

1.214

SO

2

N(CH

3

)

2

CF

2

Cl

H

H

OH

0

1.215

CCH

CF

2

Cl

H

H

OH

0

1.216

cyclopropyl

CF

2

Cl

H

H

OH

0

1.217

OPh

CF

2

Cl

H

H

OH

0

1.218

OCH

3

CF

2

Cl

H

H

OH

0

1.219

CO

2

Me

CF

2

Cl

H

H

OH

0

1.22

OCH

2

CCH

CF

2

Cl

H

H

OH

0

1.221

2-pyridyl

CF

2

Cl

H

H

OH

0

1.222

3-pyridyl

CF

2

Cl

H

H

OH

0

1.223

4-pyridyl

CF

2

Cl

H

H

OH

0

1.224

H

CF

2

Cl

H

H

OH

1

1.225

Cl

CF

2

Cl

H

H

OH

1

1.226

CHF

2

CF

2

Cl

H

H

OH

1

1.227

CCl

3

CF

2

Cl

H

H

OH

1

1.228

CClF

2

CF

2

Cl

H

H

OH

1

1.229

CF

3

CF

2

Cl

H

H

OH

1

1.23

CH

3

CF

2

Cl

H

H

OH

1

1.231

CH

2

CH

3

CF

2

Cl

H

H

OH

1

1.232

CH(CH

3

)

2

CF

2

Cl

H

H

OH

1

1.233

(CH

2

)

2

CH

3

CF

2

Cl

H

H

OH

1

1.234

C(CH

3)

3

CF

2

Cl

H

H

OH

1

1.235

CH

2

F

CF

2

Cl

H

H

OH

1

1.236

CH

2

Cl

CF

2

Cl

H

H

OH

1

1.237

CH

2

OH

CF

2

Cl

H

H

OH

1

1.238

CH

2

OCOCH

3

CF

2

Cl

H

H

OH

1

1.239

CH

2

OCOPh

CF

2

Cl

H

H

OH

1

1.24

CH

2

OCH

3

CF

2

Cl

H

H

OH

1

1.241

CH

2

OCH

2

CH

3

CF

2

Cl

H

H

OH

1

1.242

CH

2

SMe

CF

2

Cl

H

H

OH

1

1.243

CH

2

SOMe

CF

2

Cl

H

H

OH

1

1.244

CH

2

SO

2

Me

CF

2

Cl

H

H

OH

1

1.245

CH

2

SO

2

Ph

CF

2

Cl

H

H

OH

1

1.246

N(CH

3

)

2

CF

2

Cl

H

H

OH

1

1.247

CH═CH

2

CF

2

Cl

H

H

OH

1

1.248

CH

2

CH═CH

2

CF

2

Cl

H

H

OH

1

1.249

SO

2

N(CH

3

)

2

CF

2

Cl

H

H

OH

1

1.25

CCH

CF

2

Cl

H

H

OH

1

1.251

cyclopropyl

CF

2

Cl

H

H

OH

1

1.252

OPh

CF

2

Cl

H

H

OH

1

1.253

OCH

3

CF

2

Cl

H

H

OH

1

1.254

CO

2

Me

CF

2

Cl

H

H

OH

1

1.255

OCH

2

CCH

CF

2

Cl

H

H

OH

1

1.256

H

CCl

3

H

H

OH

0

1.257

Cl

CCl

3

H

H

OH

0

1.258

CH

3

CCl

3

H

H

OH

0

1.259

CH

2

CH

3

CCl

3

H

H

OH

0

1.26

CH(CH

3

)

2

CCl

3

H

H

OH

0

1.261

(CH

2

)

2

CH

3

CCl

3

H

H

OH

0

1.262

CH

2

F

CCl

3

H

H

OH

0

1.263

CH

2

Cl

CCl

3

H

H

OH

0

1.264

CH

2

OH

CCl

3

H

H

OH

0

1.265

CH

2

OCOCH

3

CCl

3

H

H

OH

0

1.266

CH

2

OCOPh

CCl

3

H

H

OH

0

1.267

CH

2

OCH

3

CCl

3

H

H

OH

0

1.268

CH

2

OCH

2

CH

3

CCl

3

H

H

OH

0

1.269

CH

2

SMe

CCl

3

H

H

OH

0

1.27

CH

2

SOMe

CCl

3

H

H

OH

0

1.271

CH

2

SO

2

Me

CCl

3

H

H

OH

0

1.272

CH

2

SO

2

Ph

CCl

3

H

H

OH

0

1.273

cyclopropyl

CCl

3

H

H

OH

0

1.274

OPh

CCl

3

H

H

OH

0

1.275

OCH

3

CCl

3

H

H

OH

0

1.276

CO

2

Me

CCl

3

H

H

OH

0

1.277

OCH

2

OCH

CCl

3

H

H

OH

0

1.278

H

CCl

3

H

H

OH

1

1.279

Cl

CCl

3

H

H

OH

1

1.28

CH

3

CCl

3

H

H

OH

1

1.281

CH

2

CH

3

CCl

3

H

H

OH

1

1.282

CH(CH

3

)

2

CCl

3

H

H

OH

1

1.283

(CH

2

)

2

CH

3

CCl

3

H

H

OH

1

1.284

CH

2

F

CCl

3

H

H

OH

1

1.285

CH

2

Cl

CCl

3

H

H

OH

1

1.286

CH

2

OH

CCl

3

H

H

OH

1

1.287

CH

2

OCOCH

3

CCl

3

H

H

OH

1

1.288

CH

2

OCOPh

CCl

3

H

H

OH

1

1.289

CH

2

OCH

3

CCl

3

H

H

OH

1

1.29

CH

2

OCH

2

CH

3

CCl

3

H

H

OH

1

1.291

CH

2

SMe

CCl

3

H

H

OH

1

1.292

CH

2

SOMe

CCl

3

H

H

OH

1

1.293

CH

2

SO

2

Me

CCl

3

H

H

OH

1

1.294

CH

2

SO

2

Ph

CCl

3

H

H

OH

1

1.295

cyclopropyl

CCl

3

H

H

OH

1

1.296

OPh

CCl

3

H

H

OH

1

1.297

OCH

3

CCl

3

H

H

OH

1

1.298

CO

2

Me

CCl

3

H

H

OH

1

1.299

OCH

2

CCH

CCl

3

H

H

OH

1

1.3

CF

3

CHF

2

H

H

OH

0

1.301

CH

3

CHF

2

H

H

OH

0

1.302

CH

2

OCH

3

CHF

2

H

H

OH

0

1.303

CH

2

Cl

CHF

2

H

H

OH

0

1.304

CH

2

F

CHF

2

H

H

OH

0

1.305

CF

3

CHF

2

H

H

OH

1

1.306

CH

3

CHF

2

H

H

OH

1

1.307

CH

2

OCH

3

CHF

2

H

H

OH

1

1.308

CH

2

Cl

CHF

2

H

H

OH

1

1.309

CH

2

F

CHF

2

H

H

OH

1

1.31

CH

3

CF

3

H

CH

3

OH

0

1.311

CH

3

CF

3

H

CH

3

OH

1

1.312

Cl

CF

3

H

CH

3

OH

0

1.313

CH

3

CF

3

CH

3

H

OH

0

1.314

CH

3

CF

3

Ph

H

OH

0

1.315

CH

3

CF

3

Cl

H

OH

0

1.316

CH

3

CF

3

CO

2

CH

2

CH

3

H

OH

0

1.317

CH

3

CF

3

CO

2

CH

2

Ph

H

OH

0

1.318

CH

3

CF

3

CH

3

H

OH

1

1.319

CH

3

CF

3

Ph

H

OH

1

1.32

CH

3

CF

3

Cl

H

OH

1

1.321

CH

3

CF

3

CO

2

CH

2

CH

3

H

OH

1

1.322

CH

3

CF

3

CO

2

CH

2

Ph

H

OH

1

1.323

OCH

3

CF

3

CH

3

H

OH

0

1.324

CH

2

OCH

3

CF

3

CH

3

H

OH

0

1.325

CH

2

OCH

3

CF

3

Ph

H

OH

0

1.326

CH

2

OCH

3

CF

3

Cl

H

OH

0

1.327

CH

2

OCH

3

CF

3

CO

2

CH

2

CH

3

H

OH

0

1.328

CH

2

OCH

3

CF

3

CO

2

CH

2

Ph

H

OH

0

1.329

CH

2

OCH

3

CF

3

CH

3

H

OH

1

1.33

CH

2

OCH

3

CF

3

Ph

H

OH

1

1.331

CH

2

OCH

3

CF

3

Cl

H

OH

1

1.332

CH

2

OCH

3

CF

3

CO

2

CH

2

CH

3

H

OH

1

1.333

CH

2

OCH

3

CF

3

CO

2

CH

2

Ph

H

OH

1

1.334

COOCH

3

H

H

H

OH

0

1.335

CF

3

SCH

3

H

H

OH

0

1.336

CH

3

SCH

3

H

H

OH

0

1.337

CF

3

SOCH

3

H

H

OH

0

1.338

CH

3

SOCH

3

H

H

OH

0

1.339

CF

3

SO

2

CH

3

H

H

OH

0

1.34

CH

3

SO

2

CH

3

H

H

OH

0

1.341

CF

3

SCH

2

CH

3

H

H

OH

0

1.342

CH

3

SCH

2

CH

3

H

H

OH

0

1.343

CF

3

SOCH

2

CH

3

H

H

OH

0

1.344

CH

3

SOCH

2

CH

3

H

H

OH

0

1.345

CF

3

SO

2

CH

2

CH

3

H

H

OH

0

1.346

CH

3

SO

2

CH

2

CH

3

H

H

OH

0

1.347

CF

3

OCH

3

H

H

OH

0

1.348

CH

3

OCH

3

H

H

OH

0

1.349

CF

3

OCH

2

CF

3

H

H

OH

0

1.35

CH

3

OCH

2

CF

3

H

H

OH

0

1.351

CF

3

OCH

2

CCH

H

H

OH

0

1.352

CH

3

OCH

2

CCH

H

H

OH

0

1.353

CF

3

CN

H

H

OH

0

1.354

CH

3

CN

H

H

OH

0

1.355

CF

3

Cl

H

H

OH

0

1.356

CF

3

Cl

H

H

O-NEt

3

+

0

1.357

CH

3

Cl

H

H

OH

0

1.358

H

Cl

H

H

OH

0

1.359

CF

3

OCH

3

H

H

OH

0

1.36

CH

3

OCH

3

H

H

OH

0

1.361

CF

3

CH

3

H

H

OH

0

1.362

H

CF

3

H

CH

3

OH

0

1.363

H

CF

3

H

CF

3

OH

0

1.364

H

CF

3

H

CH

2

CH

3

OH

0

1.365

H

CF

3

H

CF

3

OH

0

1.366

H

CF

3

H

SCH

3

OH

0

1.367

H

CF

3

H

SOCH

3

OH

0

1.368

H

CF

3

H

SO

2

CH

3

OH

0

1.369

H

CF

3

H

Cl

OH

0

1.37

H

CF

3

H

OCH

3

OH

0

1.371

H

CH

3

H

CF

3

OH

0

1.372

H

Cl

H

CF

3

OH

0

1.373

H

OCH

3

H

CF

3

OH

0

1.374

H

SCH

3

H

CF

3

OH

0

1.375

H

SOCH

3

H

CF

3

OH

0

1.376

CH

3

CF

3

H

H

O-K+

0

1.377

CH

3

CF

3

H

H

S(CH

2

)

7

CH

3

0

1.378

CH

3

CF

3

H

H

S(CH

2

)

7

CH

3

0

1.379

CH

3

CF

3

H

H

SO(CH

2

)

7

CH

3

0

1.38

CH

3

CF

3

H

H

SO

2

(CH

2

)

7

CH

3

0

1.381

CH

3

CF

3

H

H

SPh

0

1.382

CH

3

CF

3

H

H

SOPh

0

1.383

CH

3

CF

3

H

H

SO

2

Ph

0

1.384

CH

3

CF

3

H

H

NOCH

3

0

1.385

CH

3

CF

3

H

H

NOCH

2

Ph

0

1.386

CH

3

CF

3

H

H

NOCH

2

CH═CH

2

0

1.387

CH

3

CF

3

H

H

NOC(CH

3

)

3

0

1.388

CH

3

CF

3

H

H

NOCH

2

CH

3

0

1.389

CH

3

CF

3

H

H

NCH

2

CH

2

SH

0

1.39

CH

3

CF

3

H

H

NN(CH

3

)

2

0

1.391

CH

3

CF

3

H

H

NN(CH

3

)C(S)NH

2

0

1.392

CH

3

CF

3

H

H

N-morpholino

0

1.393

CH

3

CF

3

H

H

NHCOCH

3

0

1.394

CH

3

CF

3

H

H

NHCO(CH

2

)

7

CH

3

0

1.395

CH

3

CF

3

H

H

NHCOPh

0

1.396

CH

3

CF

3

H

H

NHSO

2

CH

3

0

1.397

CH

3

CF

3

H

H

NH(CO)S(CH

2

)

7

CH

3

0

1.398

CH

3

CF

3

H

H

Cl

0

1.399

CH

3

CF

3

H

H

NH

2

0

1.4

CH

3

CF

3

H

H

OCOC(CH

3

)

3

0

1.401

CH

3

CF

3

H

H

OCOCH

3

0

1.402

CH

3

CF

3

H

H

OCOPh

0

1.403

CH

3

CF

3

H

H

OCO-cyclopropyl

0

1.404

CH

3

CF

3

H

H

OCOCH

2

CH

3

0

1.405

CH

3

CF

3

H

H

OCOCH═CH

2

0

1.406

CH

3

CF

3

H

H

OCOCH═CHCH

3

0

1.407

CH

3

CF

3

H

H

O(CO)SCH

3

0

1.408

CH

3

CF

3

H

H

O(CO)S(CH

2

)

7

CH

3

0

1.409

CH

3

CF

3

H

H

O(CO)OCH

2

CH

3

0

1.41

CH

3

CF

3

H

H

O(CO)N(CH

2

CH

3

)

2

0

1.411

CH

3

(CF

2

)

3

CF

3

H

H

OH

0

1.412

CH

3

CF

3

H

H

S-(4-Cl-phenyl)

0

1.413

CH

3

CF

3

H

H

SO-(4-Cl-phenyl)

0

1.414

CH

3

CF

3

H

H

SO

2

-(4-Cl-phenyl)

0

1.415

CH

3

CF

3

H

H

S-(4-CF

3

-phenyl)

0

1.416

CH

3

CF

3

H

H

SO-(4-CF

3

-phenyl)

0

1.417

CH

3

CF

3

H

H

SO

2

-(4-CF

3

-phenyl)

0

1.418

CH

3

CF

3

H

H

S-(4-NO

2

-phenyl)

0

1.419

CH

3

CF

3

H

H

SO-(4-NO

2

-phenyl)

0

1.42

CH

3

CF

3

H

H

SO

2

-(4-NO

2

-phenyl)

0

1.421

CH

3

CF

3

H

H

0

1.422

CH

3

CF

3

H

H

0

1.423

CH

3

CF

3

H

H

0

1.424

CH

3

CF

3

H

H

0

1.425

CF

2

H

SCH

3

H

H

OH

0

1.426

CF

2

Cl

SCH

3

H

H

OH

0

1.427

CF

2

H

SOCH

3

H

H

OH

0

1.428

CF

2

Cl

SOCH

3

H

H

OH

0

1.429

CF

2

H

SO

2

CH

3

H

H

OH

0

1.43

CF

2

Cl

SO

2

CH

3

H

H

OH

0

1.431

CF

2

H

SCH

2

CH

3

H

H

OH

0

1.432

CF

2

Cl

SCH

2

CH

3

H

H

OH

0

1.433

CF

2

H

SOCH

2

CH

3

H

H

OH

0

1.434

CF

2

Cl

SOCH

2

CH

3

H

H

OH

0

1.435

CF

2

H

SO

2

CH

2

CH

3

H

H

OH

0

1.436

CF

2

Cl

SO

2

CH

2

CH

3

H

H

OH

0

1.437

CF

2

H

OCH

3

H

H

OH

0

1.438

CF

2

Cl

OCH

3

H

H

OH

0

1.439

CF

2

H

OCH

2

CF

3

H

H

OH

0

1.44

CF

2

Cl

OCH

2

CF

3

H

H

OH

0

1.441

CF

2

H

OCH

2

CCH

H

H

OH

0

1.442

CF

2

Cl

OCH

2

CCH

H

H

OH

0

1.443

CF

2

H

CN

H

H

OH

0

1.444

CF

2

Cl

CN

H

H

OH

0

1.445

CF

2

H

Cl

H

H

OH

0

1.446

CF

2

Cl

Cl

H

H

OH

0

1.447

CF

2

H

OCH

3

H

H

OH

0

1.448

CF

2

Cl

OCH

3

H

H

OH

0

1.449

CF

3

CH

2

OCH

3

H

H

OH

0

1.45

CF

3

CH

2

OCH

3

H

H

OH

1

1.451

CF

2

Cl

CH

2

OCH

3

H

H

OH

0

1.452

CF

2

Cl

CH

2

OCH

3

H

H

OH

1

1.453

CF

2

H

CH

2

OCH

3

H

H

OH

0

1.454

CF

2

H

CH

2

OCH

3

H

H

OH

1

1.455

CN

CF

3

H

H

OH

0

TABLE 2

Comp. No.

R

1

R

2

R

3

R

4

2.001

H

CF

3

H

H

2.002

F

CF

3

H

H

2.003

Cl

CF

3

H

H

2.004

Br

CF

3

H

H

2.005

CHF

2

CF

3

H

H

2.006

CCl

3

CF

3

H

H

2.007

CClF

2

CF

3

H

H

2.008

CF

3

CF

3

H

H

2.009

CH

3

CF

3

H

H

2.01

CH

2

CH

3

CF

3

H

H

2.011

CH(CH

3

)

2

CF

3

H

H

2.012

(CH

2

)

2

CH

3

CF

3

H

H

2.013

Ph

CF

3

H

H

2.014

CH

2

F

CF

3

H

H

2.015

CH

2

Cl

CF

3

H

H

2.016

CH

2

Br

CF

3

H

H

2.017

CH

2

OH

CF

3

H

H

2.018

CH

2

OCOCH

3

CF

3

H

H

2.019

CH

2

OCOPh

CF

3

H

H

2.02

CH

2

OCH

3

CF

3

H

H

2.021

CH

2

OCH

2

CH

3

CF

3

H

H

2.022

CH

2

CH

2

OCH

3

CF

3

H

H

2.023

CH

2

SMe

CF

3

H

H

2.024

CH

2

SOMe

CF

3

H

H

2.025

CH

2

SO

2

Me

CF

3

H

H

2.026

CH

2

SO

2

Ph

CF

3

H

H

2.027

SCH

2

ph

CF

3

H

H

2.028

SOCH

2

Ph

CF

3

H

H

2.029

SO

2

CH

2

Ph

CF

3

H

H

2.03

SCH

3

CF

3

H

H

2.031

SOCH

3

CF

3

H

H

2.032

SO

2

CH

3

CF

3

H

H

2.033

N(CH

3

)

2

CF

3

H

H

2.034

CH═CH

2

CF

3

H

H

2.035

CH

2

CH═CH

2

CF

3

H

H

2.036

SO

2

N(CH

3

)

2

CF

3

H

H

2.037

CCH

CF

3

H

H

2.038

OCH

3

CF

3

H

H

2.039

OPh

CF

3

H

H

2.04

OCHF

2

CF

3

H

H

2.041

CO

2

Me

CF

3

H

H

2.042

OCH

2

CCH

CF

3

H

H

2.043

OCH

2

CF

3

CF

3

H

H

2.044

H

CF

3

H

Cl

2.045

F

H

Cl

2.046

CN

CF

3

H

H

2.047

H

CHF

2

H

H

2.048

CH

3

CHF

2

H

H

2.049

CH

2

CH

3

CHF

2

H

H

2.05

CH

2

OCH

3

CHF

2

H

H

2.051

H

CF

2

Cl

H

H

2.052

CH

3

CF

2

Cl

H

H

2.053

CH

2

CH

3

CF

2

Cl

H

H

2.054

CH

2

OCH

3

CF

2

Cl

H

H

TABLE 3

Comp. No.

R

1

R

2

R

3

R

4

3.001

H

CF

3

H

H

3.002

F

CF

3

H

H

3.003

Cl

CF

3

H

H

3.004

Br

CF

3

H

H

3.005

CHF

2

CF

3

H

H

3.006

CCl

3

CF

3

H

H

3.007

CClF

2

CF

3

H

H

3.008

CF

3

CF

3

H

H

3.009

CH

3

CF

3

H

H

3.01

CH

2

CH

3

CF

3

H

H

3.011

CH(CH

3

)

2

CF

3

H

H

3.012

(CH

2

)

2

CH

3

CF

3

H

H

3.013

Ph

CF

3

H

H

3.014

CH

2

F

CF

3

H

H

3.015

CH

2

Cl

CF

3

H

H

3.016

CH

2

Br

CF

3

H

H

3.017

CH

2

OH

CF

3

H

H

3.018

CH

2

OCOCH

3

CF

3

H

H

3.019

CH

2

OCOPh

CF

3

H

H

3.02

CH

2

OCH

3

CF

3

H

H

3.021

CH

2

OCH

2

CH

3

CF

3

H

H

3.022

CH

2

CH

2

OCH

3

CF

3

H

H

3.023

CH

2

SMe

CF

3

H

H

3.024

CH

2

SOMe

CF

3

H

H

3.025

CH

2

SO

2

Me

CF

3

H

H

3.026

CH

2

SO

2

Ph

CF

3

H

H

3.027

SCH

2

Ph

CF

3

H

H

3.028

SOCH

2

Ph

CF

3

H

H

3.029

SO

2

CH

2

Ph

CF

3

H

H

3.03

SCH

3

CF

3

H

H

3.031

SOCH

3

CF

3

H

H

3.032

SO

2

CH

3

CF

3

H

H

3.033

N(CH

3

)

2

CF

3

H

H

3.034

CH═CH

2

CF

3

H

H

3.035

CH

2

CH═CH

2

CF

3

H

H

3.036

SO

2

N(CH

3

)

2

CF

3

H

H

3.037

CCH

CF

3

H

H

3.038

OCH

3

CF

3

H

H

3.039

OPh

CF

3

K

H

3.04

OCHF

2

CF

3

H

H

3.041

CO

2

Me

CF

3

H

H

3.042

OCH

2

CCH

CF

3

H

H

3.043

OCH

2

CF

3

CF

3

H

H

3.044

H

CF

3

H

H

3.045

CN

CF

3

H

H

3.046

H

CHF

2

H

H

3.047

CH

3

CHF

2

H

H

3.048

CH

2

CH

3

CHF

2

H

H

3.049

CH

2

OCH

3

CHF

2

H

H

3.05

H

CF

2

Cl

H

H

3.051

CH

3

CF

2

Cl

H

H

3.052

CH

2

CH

3

CF

2

Cl

H

H

3.053

CH

2

OCH

3

CF

2

Cl

H

H

3.054

Cl

CH

3

H

H

3.055

CN

SCH

3

H

H

3.056

CN

SO

2

CH

3

H

H

TABLE 4

Comp.

No.

R

1

R

2

R

3

R

4

R

5

P

4.001

H

CF

3

H

H

OH

0

4.002

F

CF

3

H

H

OH

0

4.003

Cl

CF

3

H

H

OH

0

4.004

Br

CF

3

H

H

OH

0

4.005

CHF

2

CF

3

H

H

OH

0

4.006

CCl

3

CF

3

H

H

OH

0

4.007

CClF

2

CF

3

H

H

OH

0

4.008

CF

3

CF

3

H

H

OH

0

4.009

CH

3

CF

3

H

H

OH

0

4.01

CH

2

CH

3

CF

3

H

H

OH

0

4.011

CH(CH

3

)

2

CF

3

H

H

OH

0

4.012

(CH

2

)

2

CH

3

CF

3

H

H

OH

0

4.013

C(CH

3

)

3

CF

3

H

H

OH

0

4.014

Ph

CF

3

H

H

OH

0

4.015

CH

2

F

CF

3

H

H

OH

0

4.016

CH

2

Cl

CF

3

H

H

OH

0

4.017

CH

2

Br

CF

3

H

H

OH

0

4.018

CH

2

OH

CF

3

H

H

OH

0

4.019

CH

2

OCOCH

3

CF

3

H

H

OH

0

4.02

CH

2

OCOPh

CF

3

H

H

OH

0

4.021

CH

2

OCH

3

CF

3

H

H

OH

0

4.022

CH

2

OCH

2

CH

3

CF

3

H

H

OH

0

4.023

CH

2

CH

2

OCH

3

CF

3

H

H

OH

0

4.024

CH

2

SMe

CF

3

H

H

OH

0

4.025

CH

2

SOMe

CF

3

H

H

OH

0

4.026

CH

2

SO

2

Me

CF

3

H

H

OH

0

4.027

CH

2

SO

2

Ph

CF

3

H

H

OH

0

4.028

N(CH

3

)

2

CF

3

H

H

OH

0

4.029

CH═CH

2

CF

3

H

H

OH

0

4.03

CH

2

CH═CH

2

CF

3

H

H

OH

0

4.031

SO

2

N(CH

3

)

2

CF

3

H

H

OH

0

4.032

CCH

CF

3

H

H

OH

0

4.033

cyclopropyl

CF

3

H

H

OH

0

4.034

OCH

3

CF

3

H

H

OH

0

4.035

OPh

CF

3

H

H

OH

0

4.036

OCHF

2

CF

3

H

H

OH

0

4.037

CO

2

Me

CF

3

H

H

OH

0

4.038

OCH

2

CCH

CF

3

H

H

OH

0

4.039

H

CF

3

H

H

OH

1

4.04

F

CF

3

H

H

OH

1

4.041

Cl

CF

3

H

H

OH

1

4.042

Br

CF

3

H

H

OH

1

4.043

CHF

2

CF

3

H

H

OH

1

4.044

Cl

3

CF

3

H

H

OH

1

4.045

CClF

2

CF

3

H

H

OH

1

4.046

CF

3

CF

3

H

H

OH

1

4.047

CH

3

CF

3

H

H

OH

1

4.048

CH

2

CH

3

CF

3

H

H

OH

1

4.049

CH(CH

3

)

2

CF

3

H

H

OH

1

4.05

(CH

2

)

2

CH

3

CF

3

H

H

OH

1

4.051

C(CH

3

)

3

CF

3

H

H

OH

1

4.052

Ph

CF

3

H

H

OH

1

4.053

CH

2

F

CF

3

H

H

OH

1

4.054

CH

2

Cl

CF

3

H

H

OH

1

4.055

CH

2

Br

CF

3

H

H

OH

1

4.056

CH

2

OH

CF

3

H

H

OH

1

4.057

CH

2

OCOCH

3

CF

3

H

H

OH

1

4.058

CH

2

OCOPh

CF

3

H

H

OH

1

4.059

CH

2

OCH

3

CF

3

H

H

OH

1

4.06

CH

2

OCH

2

CH

3

CF

3

H

H

OH

1

4.061

CH

2

CH

2

OCH

3

CF

3

H

H

OH

1

4.062

CH

2

SMe

CF

3

H

H

OH

1

4.063

CH

2

SOMe

CF

3

H

H

OH

1

4.064

CH

2

SO

2

Me

CF

3

H

H

OH

1

4.065

CH

2

SO

2

Ph

CF

3

H

H

OH

1

4.066

N(CH

3)

2

CF

3

H

H

OH

1

4.067

CH═CH

2

CF

3

H

H

OH

1

4.068

CH

2

CH═CH

2

CF

3

H

H

OH

1

4.069

SO

2

N(CH

3

)

2

CF

3

H

H

OH

1

4.07

CCH

CF

3

H

H

OH

1

4.071

cyclopropyl

CF

3

H

H

OH

1

4.072

OCH

3

CF

3

H

H

OH

1

4.073

OPh

CF

3

H

H

OH

1

4.074

OCHF

2

CF

3

H

H

OH

1

4.075

CO

2

Me

CF

3

H

H

OH

1

4.076

2-furyl

CF

3

H

H

OH

1

4.077

OCH

2

CCH

CF

3

H

H

OH

1

4.078

H

CF

2

CF

3

H

H

OH

0

4.079

Cl

CF

2

CF

3

H

H

OH

0

4.08

CHF

2

CF

2

CF

3

H

H

OH

0

4.081

CCl

3

CF

2

CF

3

H

H

OH

0

4.082

CClF

2

CF

2

CF

3

H

H

OH

0

4.083

CF

3

CF

2

CF

3

H

H

OH

0

4.084

CH

3

CF

2

CF

3

H

H

OH

0

4.085

CH

2

CH

3

CF

2

CF

3

H

H

OH

0

4.086

CH(CH

3

)

2

CF

2

CF

3

H

H

OH

0

4.087

(CH

2

)

2

CH

3

CF

2

CF

3

H

H

OH

0

4.088

C(CH

3

)

3

CF

2

CF

3

H

H

OH

0

4.089

CH

2

F

CF

2

CF

3

H

H

OH

0

4.09

CH

2

Cl

CF

2

CF

3

H

H

OH

0

4.091

CH

2

OH

CF

2

CF

3

H

H

OH

0

4.092

CH

2

OCOCH

3

CF

2

CF

3

H

H

OH

0

4.093

CH

2

OCOPh

CF

2

CF

3

H

H

OH

0

4.094

CH

2

OCH

3

CF

2

CF

3

H

H

OH

0

4.095

CH

2

OCH

2

CH

3

CF

2

CF

3

H

H

OH

0

4.096

CH

2

SMe

CF

2

CF

3

H

H

OH

0

4.097

CH

2

SOMe

CF

2

CF

3

H

H

OH

0

4.098

CH

2

SO

2

Me

CF

2

CF

3

H

H

OH

0

4.099

CH

2

SO

2

Ph

CF

2

CF

3

H

H

OH

0

4.1

N(CH

3

)

2

CF

2

CF

3

H

H

OH

0

4.101

CH═CH

2

CF

2

CF

3

H

H

OH

0

4.102

CH

2

CH═CH

2

CF

2

CF

3

H

H

OH

0

4.103

SO

2

N(CH

3

)

2

CF

2

CF

3

H

H

OH

0

4.104

CCH

CF

2

CF

3

H

H

OH

0

4.105

cyclopropyl

CF

2

CF

3

H

H

OH

0

4.106

OPh

CF

2

CF

3

H

H

OH

0

4.107

OCH

3

CF

2

CF

3

H

H

OH

0

4.108

CO

2

Me

CF

2

CF

3

H

H

OH

0

4.109

OCH

2

CCH

CF

2

CF

3

H

H

OH

0

4.11

H

CF

2

CF

2

CF

3

H

H

OH

0

4.111

CHF

2

CF

2

CF

2

CF

3

H

H

OH

0

4.112

CF

3

CF

2

CF

2

CF

3

H

H

OH

0

4.113

CH

3

CF

2

CF

2

CF

3

H

H

OH

0

4.114

CH

2

CH

3

CF

2

CF

2

CF

3

H

H

OH

0

4.115

(CH

2

)

2

CH

3

CF

2

CF

2

CF

3

H

H

OH

0

4.116

CH

2

Cl

CF

2

CF

2

CF

3

H

H

OH

0

4.117

CH

2

OCH

3

CF

2

CF

2

CF

3

H

H

OH

0

4.118

H

CF

2

Cl

H

H

OH

0

4.119

Cl

CF

2

Cl

H

H

OH

0

4.12

CHF

2

CF

2

Cl

H

H

OH

0

4.121

CCl

3

CF

2

Cl

H

H

OH

0

4.122

CClF

2

CF

2

Cl

H

H

OH

0

4.123

CF

3

CF

2

Cl

H

H

OH

0

4.124

CH

3

CF

2

Cl

H

H

OH

0

4.125

CH

2

CH

3

CF

2

Cl

H

H

OH

0

4.126

CH(CH

3

)

2

CF

2

Cl

H

H

OH

0

4.127

(CH

2

)

2

CH

3

CF

2

Cl

H

H

OH

0

4.128

C(CH

3

)

3

CF

2

Cl

H

H

OH

0

4.129

CH

2

F

CF

2

Cl

H

H

OH

0

4.13

CH

2

Cl

CF

2

Cl

H

H

OH

0

4.131

CH

2

OH

CF

2

Cl

H

H

OH

0

4.132

CH

2

OCOCH

3

CF

2

Cl

H

H

OH

0

4.133

CH

2

OCOPh

CF

2

Cl

H

H

OH

0

4.134

CH

2

OCH

3

CF

2

Cl

H

H

OH

0

4.135

CH

2

OCH

2

CH

3

CF

2

Cl

H

H

OH

0

4.136

CH

2

SMe

CF

2

Cl

H

H

OH

0

4.137

CH

2

SOMe

CF

2

Cl

H

H

OH

0

4.138

CH

2

SO

2

Me

CF

2

Cl

H

H

OH

0

4.139

CH

2

SO

2

Ph

CF

2

Cl

H

H

OH

0

4.14

N(CH

3

)

2

CF

2

Cl

H

H

OH

0

4.141

CH═CH

2

CF

2

Cl

H

H

OH

0

4.142

CH

2

CH═CH

2

CF

2

Cl

H

H

OH

0

4.143

SO

2

N(CH

3

)

2

CF

2

Cl

H

H

OH

0

4.144

CCH

CF

2

Cl

H

H

OH

0

4.145

cyclopropyl

CF

2

Cl

H

H

OH

0

4.146

OPh

CF

2

Cl

H

H

OH

0

4.147

OCH

3

CF

2

Cl

H

H

OH

0

4.148

CO

2

Me

CF

2

Cl

H

H

OH

0

4.149

OCH

2

CCH

CF

2

Cl

H

H

OH

0

4.15

CH

3

CF

2

Cl

H

H

OH

1

4.151

CH

2

OCH

3

CF

2

Cl

H

H

OH

1

4.152

H

CCl

3

H

H

OH

0

4.153

Cl

CCl

3

H

H

OH

0

4.154

CH

3

CCl

3

H

H

OH

0

4.155

CH

2

CH

3

CCl

3

H

H

OH

0

4.156

CH(CH

3

)

2

CCl

3

H

H

OH

0

4.157

(CH

2

)

2

CH

3

CCl

3

H

H

OH

0

4.158

CH

2

F

CCl

3

H

H

OH

0

4.159

CH

2

Cl

CCl

3

H

H

OH

0

4.16

CH

2

OH

CCl

3

H

H

OH

0

4.161

CH

2

OCOCH

3

CCl

3

H

H

OH

0

4.162

CH

2

OCOPh

CCl

3

H

H

OH

0

4.163

CH

2

OCH

3

CCl

3

H

H

OH

0

4.164

CH

2

OCH

2

CH

3

CCl

3

H

H

OH

0

4.165

CH

2

SMe

CCl

3

H

H

OH

0

4.166

CH

2

SOMe

CCl

3

H

H

OH

0

4.167

CH

2

SO

2

Me

CCl

3

H

H

OH

0

4.168

CH

2

SO

2

Ph

CCl

3

H

H

OH

0

4.169

cyclopropyl

CCl

3

H

H

OH

0

4.17

OPh

CCl

3

H

H

OH

0

4.171

OCH

3

CCl

3

H

H

OH

0

4.172

CO

2

Me

CCl

3

H

H

OH

0

4.173

OCH

2

CCH

CCl

3

H

H

OH

0

4.174

CF

3

CHF

2

H

H

OH

0

4.175

CH

3

CHF

2

H

H

OH

0

4.176

CH

2

OCH

3

CHF

2

H

H

OH

0

4.177

CH

2

Cl

CHF

2

H

H

OH

0

4.178

CH

2

F

CHF

2

H

H

OH

0

4.179

CF

3

CHF

2

H

H

OH

1

4.18

CH

3

CHF

2

H

H

OH

1

4.181

CH

2

OCH

3

CHF

2

H

H

OH

1

4.182

CH

2

Cl

CHF

2

H

H

OH

1

4.183

CH

2

F

CHF

2

H

H

OH

1

4.184

CH

3

CF

3

H

CH

3

OH

0

4.185

CH

3

CF

3

H

CH

3

OH

1

4.186

Cl

CF

3

H

CH

3

OH

0

4.187

CH

3

CF

3

CH

3

H

OH

0

4.188

CH

3

CF

3

Ph

H

OH

0

4.189

CH

3

CF

3

Cl

H

OH

0

4.19

CH

3

CF

3

CO

2

CH

2

CH

3

H

OH

0

4.191

CH

3

CF

3

CO

2

CH

2

Ph

H

OH

0

4.192

CH

3

CF

3

CH

3

H

OH

1

4.193

CH

3

CF

3

Ph

H

OH

1

4.194

CH

3

CF

3

Cl

H

OH

1

4.195

CH

3

CF

3

CO

2

CH

2

CH

3

H

OH

1

4.196

CH

3

CF

3

OC

2

CH

2

Ph

H

OH

1

4.197

OCH

3

CF

3

CH

3

H

OH

0

4.198

CH

2

OCH

3

CF

3

CH

3

H

OH

0

4.199

CH

2

OCH

3

CF

3

Ph

H

OH

0

4.2

CH

2

OCH

3

CF

3

Cl

H

OH

0

4.201

CH

2

OCH

3

CF

3

CO

2

CH

2

CH

3

H

OH

0

4.202

CH

2

OCH

3

CF

3

CO

2

CH

2

Ph

H

OH

0

4.203

CH

2

OCH

3

CF

3

CH

3

H

OH

1

4.204

CH

2

OCH

3

CF

3

Ph

H

OH

1

4.205

CH

2

OCH

3

CF

3

Cl

H

OH

1

4.206

CH

2

OCH

3

CF

3

CO

2

CH

2

CH

3

H

OH

1

4.207

CH

2

OCH

3

CF

3

CO

2

CH

2

Ph

H

OH

1

4.208

COOCH

3

H

H

H

OH

0

4.209

CF

3

SCH

3

H

H

OH

0

4.21

CH

3

SCH

3

H

H

OH

0

4.211

CF

3

SOCH

3

H

H

OH

0

4.212

CH

3

SOCH

3

H

H

OH

0

4.213

CF

3

SO

2

CH

3

H

H

OH

0

4.214

CH

3

SO

2

CH

3

H

H

OH

0

4.215

CF

3

SCH

2

CH

3

H

H

OH

0

4.216

CH

3

SCH

2

CH

3

H

H

OH

0

4.217

CF

3

SOCH

2

CH

3

H

H

OH

0

4.218

CH

3

SOCH

2

CH

3

H

H

OH

0

4.219

CF

3

SO

2

CH

2

CH

3

H

H

OH

0

4.22

CH

3

SO

2

CH

2

CH

3

H

H

OH

0

4.221

CF

3

OCH

3

H

H

OH

0

4.222

CH

3

OCH

3

H

H

OH

0

4.223

CF

3

OCH

2

CF

3

H

H

OH

0

4.224

CH

3

OCH

2

CF

3

H

H

OH

0

4.225

CF

3

OCH

2

CCH

H

H

OH

0

4.226

CH

3

OCH

2

CCH

H

H

OH

0

4.227

CF

3

CN

H

H

OH

0

4.228

CH

3

CN

H

H

OH

0

4.229

CF

3

Cl

H

H

OH

0

4.23

CH

3

Cl

H

H

OH

0

4.231

H

Cl

H

H

OH

0

4.232

CF

3

OCH

3

H

H

OH

0

4.233

CH

3

OCH

3

H

H

OH

0

4.234

CF

3

CH

3

H

H

OH

0

4.235

H

CF

3

H

CH

3

OH

0

4.236

H

CF

3

H

CF

3

OH

0

4.237

H

CF

3

H

CH

2

CH

3

OH

0

4.238

H

CF

3

H

CF

3

OH

0

4.239

H

CF

3

H

SCH

3

OH

0

4.24

H

CF

3

H

SOCH

3

OH

0

4.241

H

CF

3

H

SO

2

CH

3

OH

0

4.242

H

CF

3

H

Cl

OH

0

4.243

H

CF

3

H

OCH

3

OH

0

4.244

H

CH

3

H

CF

3

OH

0

4.245

H

Cl

H

CF

3

OH

0

4.246

H

OCH

3

H

CF

3

OH

0

4.247

H

SCH

3

H

CF

3

OH

0

4.248

H

SOCH

3

H

CF

3

OH

0

4.249

CH

3

CF

3

H

H

S(CH

2

)

7

CH

3

0

4.25

CH

3

CF

3

H

H

S(CH

2

)

7

CH

3

0

4.251

CH

3

CF

3

H

H

SO(CH

2

)

7

CH

3

0

4.252

CH

3

CF

3

H

H

SO

2

(CH

2

)

7

CH

3

0

4.253

CH

3

CF

3

H

H

SPh

0

4.254

CH

3

CF

3

H

H

SOPh

0

4.255

CH

3

CF

3

H

H

SO

2

Ph

0

4.256

CH

3

CF

3

H

H

NOCH

3

0

4.257

CH

3

CF

3

H

H

NOCH

2

Ph

0

4.258

CH

3

CF

3

H

H

NOCH

2

CH═CH

2

0

4.259

CH

3

CF

3

H

H

NOC(CH

3

)

3

0

4.26

CH

3

CF

3

H

H

NOCH

2

CH

3

0

4.261

CH

3

CF

3

H

H

NCH

2

CH

2

SH

0

4.262

CH

3

CF

3

H

H

NN(CH

3

)

2

0

4.263

CH

3

CF

3

H

H

NN(CH

3

)C(S)NH

2

0

4.264

CH

3

CF

3

H

H

N-morpholino

0

4.265

CH

3

CF

3

H

H

NHCOCH

3

0

4.266

CH

3

CF

3

H

H

NHCO(CH

2

)

7

CH

3

0

4.267

CH

3

CF

3

H

H

NHCOPh

0

4.268

CH

3

CF

3

H

H

NHSO

2

CH

3

0

4.269

CH

3

CF

3

H

H

NH(CO)S(CH

2

)

7

CH

3

0

4.27

CH

3

CF

3

H

H

Cl

0

4.271

CH

3

CF

3

H

H

NH

2

0

4.272

CH

3

CF

3

H

H

OCOC(CH

3)

3

0

4.273

CH

3

CF

3

H

H

OCOCH

3

0

4.274

CH

3

CF

3

H

H

OCOPh

0

4.275

CH

3

CF

3

H

H

OCO-cyclopropyl

0

4.276

CH

3

CF

3

H

H

OCOCH

2

CH

3

0

4.277

CH

3

CF

3

H

H

OCOCH═CH

2

0

4.278

CH

3

CF

3

H

H

OCOCH═CHCH

3

0

4.279

CH

3

CF

3

H

H

O(CO)SCH

3

0

4.28

CH

3

CF

3

H

H

O(CO)S(CH

2

)

7

CH

3

0

4.281

CH

3

CF

3

H

H

O(CO)OCH

2

CH

3

0

4.282

CH

3

CF

3

H

H

O(CO)N(CH

2

CH

3

)

2

0

4.283

CH

3

(CF

2

)

3

CF

3

H

H

OH

0

4.284

CH

3

CF

3

H

H

S-(4-Cl-phenyl)

0

4.285

CH

3

CF

3

H

H

SO-(4-Cl-phenyl)

0

4.286

CH

3

CF

3

H

H

SO

2

-(4-Cl-phenyl)

0

4.287

CH

3

CF

3

H

H

S-(4-CF

3

-phenyl)

0

4288

CH

3

CF

3

H

H

SO-(4-CF

3

-phenyl)

0

4.289

CH

3

CF

3

H

H

SO

2

-(4-CF

3

-phenyl)

0

4.29

CH

3

CF

3

H

H

S-(4-NO

2

-phenyl)

0

4.291

CH

3

CF

3

H

H

SO-(4-NO

2

-phenyl)

0

4.292

CH

3

CF

3

H

H

SO

2

-(4-NO

2

-phenyl)

0

4.293

CH

3

CF

3

H

H

0

4.294

CH

3

CF

3

H

H

0

4.295

CH

3

CF

3

H

H

0

4.296

CH

3

CF

3

H

H

0

4.297

CF

2

H

SCH

3

H

H

OH

0

4.298

CF

2

Cl

SCH

3

H

H

OH

0

4.299

CF

2

H

SOCH

3

H

H

OH

0

4.3

CF

2

Cl

SOCH

3

H

H

OH

0

4.301

CF

2

H

SO

2

CH

3

H

H

OH

0

4.302

CF

2

Cl

SO

2

CH

3

H

H

OH

0

4.303

CF

2

H

SCH

2

CH

3

H

H

OH

0

4.304

CF

2

Cl

SCH

2

CH

3

H

H

OH

0

4.305

CF

2

H

SOCH

2

CH

3

H

H

OH

0

4.306

CF

2

Cl

SOCH

2

CH

3

H

H

OH

0

4.307

CF

2

H

SO

2

CH

2

CH

3

H

H

OH

0

4.308

CF

2

Cl

SO

2

CH

2

CH

3

H

H

OH

0

4.309

CF

2

H

OCH

3

H

H

OH

0

4.31

CF

2

Cl

OCH

3

H

H

OH

0

4.311

CF

2

H

OCH

2

CF

3

H

H

OH

0

4.312

CF

2

Cl

OCH

2

CF

3

H

H

OH

0

4.313

CF

2

H

OCH

2

CCH

H

H

OH

0

4.314

CF

2

Cl

OCH

2

CCH

H

H

OH

0

4.315

CF

2

H

CN

H

H

OH

0

4.316

CF

2

Cl

CN

H

H

OH

0

4.317

CF

2

H

Cl

H

H

OH

0

4.318

CF

2

Cl

Cl

H

H

OH

0

4.319

CF

2

H

OCH

3

H

H

OH

0

4.32

CF

2

Cl

OCH

3

H

H

OH

0

4.321

CF

3

CH

2

OCH

3

H

H

OH

0

4.322

CF

3

CH

2

OCH

3

H

H

OH

1

4.323

CF

2

Cl

CH

2

OCH

3

H

H

OH

0

4.324

CF

2

Cl

CH

2

OCH

3

H

H

OH

1

4.325

CF

2

H

CH

2

OCH

3

H

H

OH

0

4.326

CF

2

H

CH

2

OCH

3

H

H

OH

1

4.327

CN

CF

3

H

H

OH

0

4.328

SCH

3

H

H

H

OH

0

TABLE 5

Comp. No.

R

1

R

2

R

3

R

4

R

5

5.001

H

CF

3

H

H

CH

3

5.002

F

CF

3

H

H

CH

3

5.003

Cl

CF

3

H

H

CH

3

5.004

CHF

2

CF

3

H

H

CH

3

5.005

CCl

3

CF

3

H

H

CH

3

5.006

CClF

2

CF

3

H

H

CH

3

5.007

CF

3

CF

3

H

H

CH

3

5.008

CH

3

CF

3

H

H

CH

3

5.009

CH

2

CH

3

CF

3

H

H

CH

3

5.01

CH(CH

3

)2

CF

3

H

H

CH

3

5.011

(CH

2

)

2

CH

3

CF

3

H

H

CH

3

5.012

CH

2

F

CF

3

H

H

CH

3

5.013

CH

2

Cl

CF

3

H

H

CH

3

5.014

CH

2

Br

CF

3

H

H

CH

3

5.015

CH

2

OCOCH

3

CF

3

H

H

CH

3

5.016

CH

2

OCH

3

CF

3

H

H

CH

3

5.017

CH

2

CH

2

OCH

3

CF

3

H

H

CH

3

5.018

CH

2

SMe

CF

3

H

H

CH

3

5.019

CH

2

SOMe

CF

3

H

H

CH

3

5.02

CH

2

SO

2

Me

CF

3

H

H

CH

3

5.021

N(CH

3

)

2

CF

3

H

H

CH

3

5.022

CH═CH

2

CF

3

H

H

CH

3

5.023

CH

2

CH═CH

2

CF

3

H

H

CH

3

5.024

SO

2

N(CH

3

)

2

CF

3

H

H

CH

3

5.025

CCH

CF

3

H

H

CH

3

5.026

cyclopropyl

CF

3

H

H

CH

3

5.027

OCH

3

CF

3

H

H

CH

3

5.028

OPh

CF

3

H

H

CH

3

5.029

OCHF

2

CF

3

H

H

CH

3

5.03

CO

2

Me

CF

3

H

H

CH

3

5.031

OCH

2

CCH

CF

3

H

H

CH

3

5.032

CF

3

SCH

3

H

H

CH

3

5.033

CH

3

SCH

3

H

H

CH

3

5.034

CF

3

SOCH

3

H

H

CH

3

5.035

CH

3

SOCH

3

H

H

CH

3

5.036

CF

3

SO

2

CH

3

H

H

CH

3

5.037

CH

3

SO

2

CH

3

H

H

CH

3

5.038

CF

3

OCH

3

H

H

CH

3

5.039

CH

3

OCH

3

H

H

CH

3

5.04

CF

3

OCH

2

CF

3

H

H

CH

3

5.041

CH

3

OCH

2

CF

3

H

H

CH

3

5.042

CF

3

OCH

2

CCH

H

H

CH

3

5.043

CH

3

OCH

2

CCH

H

H

CH

3

5.044

CF

3

CN

H

H

CH

3

5.045

CH

3

CN

H

H

CH

3

5.046

CF

3

Cl

H

H

CH

3

5.047

CH

3

Cl

H

H

CH

3

5.048

H

Cl

H

H

CH

3

5.049

CF

3

OCH

3

H

H

CH

3

5.05

CH

3

OCH

3

H

H

CH

3

5.051

CF

3

CH

3

H

H

CH

3

5.052

H

CF

3

H

CH

3

CH

3

5.053

H

CF

3

H

CF

3

CH

3

5.054

H

CF

3

H

CH

2

CH

3

CH

3

5.055

H

CF

3

H

CF

3

CH

3

5.056

H

CF

3

H

SCH

3

CH

3

5.057

H

CF

3

H

SOCH

3

CH

3

5.058

H

CF

3

H

SO

2

CH

3

CH

3

5.059

H

CF

3

H

Cl

CH

3

5.06

H

CF

3

H

OCH

3

CH

3

5.061

H

CH

3

H

CF

3

CH

3

5.062

H

Cl

H

CF

3

CH

3

5.063

H

OCH

3

H

CF

3

CH

3

5.064

H

SCH

3

H

CF

3

CH

3

5.065

H

SOCH

3

H

CF

3

CH

3

5.066

CF

2

Cl

CH

3

H

H

CH

3

5.067

CF

2

Cl

CH

2

CH

3

H

H

CH

3

5.068

CF

2

Cl

SCH

3

H

H

CH

3

5.069

CF

2

Cl

SOCH

3

H

H

CH

3

5.07

CF

2

Cl

SO

2

CH

3

H

H

CH

3

5.071

CF

2

Cl

OCH

3

H

H

CH

3

5.072

CF

2

Cl

OCH

2

CF

3

H

H

CH

3

5.073

CF

2

Cl

OCH

2

CCH

H

H

CH

3

5.074

CF

2

Cl

CN

H

H

CH

3

5.075

CF

2

Cl

Cl

H

H

CH

3

5.076

CF

2

Cl

OCH

3

H

H

CH

3

5.077

CF

3

CH

2

OCH

3

H

H

CH

3

5.078

CF

2

Cl

CH

2

OCH

3

H

H

CH

3

5.079

CF

2

H

CH

2

OCH

3

H

H

CH

3

5.08

CN

CF

3

H

H

CH

3

5.081

CH

3

CF

3

H

H

CH

2

CH

3

5.082

CH

3

CF

3

H

H

SCH

3

5.083

CH

3

CF

3

H

H

SOCH

3

5.084

CH

3

CF

3

H

H

SO

2

CH

3

5.085

CH

3

CF

3

H

H

H

TABLE 6

Comp. No.

R

1

R

2

R

3

R

4

R

5

6.001

Cl

CF

3

H

H

CH

2

CH

3

6.002

CHF

2

CF

3

H

H

CH

2

CH

3

6.003

CCl

3

CF

3

H

H

CH

2

CH

3

6.004

CClF

2

CF

3

H

H

CH

2

CH

3

6.005

CF

3

CF

3

H

H

CH

2

CH

3

6.006

CH

3

CF

3

H

H

CH

2

CH

3

6.007

CH

2

CH

3

CF

3

H

H

CH

2

CH

3

6.008

(CH

2

)

2

CH

3

CF

3

H

H

CH

2

CH

3

6.009

CH

2

F

CF

3

H

H

CH

2

CH

3

6.01

CH

2

Cl

CF

3

H

H

CH

2

CH

3

6.011

CH

2

OCH

3

CF

3

H

H

CH

2

CH

3

6.012

CH

2

SMe

CF

3

H

H

CH

2

CH

3

6.013

CH

2

SO

2

Me

CF

3

H

H

CH

2

CH

3

6.014

CH═CH

2

CF

3

H

H

CH

2

CH

3

6.015

CH

2

CH═CH

2

CF

3

H

H

CH

2

CH

3

6.016

CCH

CF

3

H

H

CH

2

CH

3

6.017

CF

3

SCH

3

H

H

CH

2

CH

3

6.018

CF

3

SOCH

3

H

H

CH

2

CH

3

6.019

CF

3

SO

2

CH

3

H

H

CH

2

CH

3

6.02

CF

3

OCH

3

H

H

CH

2

CH

3

6.021

CF

3

CN

H

H

CH

2

CH

3

6.022

CF

3

Cl

H

H

CH

2

CH

3

6.023

CF

3

OCH

3

H

H

CH

2

CH

3

6.024

CF

3

CH

3

H

H

CH

2

CH

3

6.025

H

CF

3

H

CH

3

CH

2

CH

3

6.026

H

CF

3

H

CF

3

CH

2

CH

3

6.027

H

CF

3

H

SCH

3

CH

2

CH

3

6.028

H

CF

3

H

SOCH

3

CH

2

CH

3

6.029

H

CF

3

H

SO

2

CH

3

CH

2

CH

3

6.03

H

CF

3

H

Cl

CH

2

CH

3

6.031

H

CF

3

H

OCH

3

CH

2

CH

3

6.032

H

CH

3

H

CF

3

CH

2

CH

3

6.033

H

Cl

H

CF

3

CH

2

CH

3

6.034

H

OCH

3

H

CF

3

CH

2

CH

3

6.035

CN

CF

3

H

H

CH

2

CH

3

6.036

Cl

CF

3

H

H

CH(CH

3

)

2

6.037

CHF

2

CF

3

H

H

CH(CH

3

)

2

6.038

CCl

3

CF

3

H

H

CH(CH

3

)

2

6.039

CClF

2

CF

3

H

H

CH(CH

3

)

2

6.04

CF

3

CF

3

H

H

CH(CH

3

)

2

6.041

CH

3

CF

3

H

H

CH(CH

3

)

2

6.042

CH

2

CH

3

CF

3

H

H

CH(CH

3

)

2

6.043

(CH

2

)

2

CH

3

CF

3

H

H

CH(CH

3

)

2

6.044

CH

2

F

CF

3

H

H

CH(CH

3

)

2

6.045

CH

2

Cl

CF

3

H

H

CH(CH

3

)

2

6.046

CH

2

OCH

3

CF

3

H

H

CH(CH

3

)

2

6.047

CH

2

SMe

CF

3

H

H

CH(CH

3

)

2

6.048

CH

2

SO

2

Me

CF

3

H

H

CH(CH

3

)

2

6.049

CH═CH

2

CF

3

H

H

CH(CH

3

)

2

6.05

CH

2

CH═CH

2

CF

3

H

H

CH(CH

3

)

2

6.051

CCH

CF

3

H

H

CH(CH

3

)

2

6.052

CF

3

SCH

3

H

H

CH(CH

3

)

2

6.053

CF

3

SOCH

3

H

H

CH(CH

3

)

2

6.054

CF

3

SO

2

CH

3

H

H

CH(CH

3

)

2

6.055

CF

3

OCH

3

H

H

CH(CH

3

)

2

6.056

CF

3

CN

H

H

CH(CH

3

)

2

6.057

CF

3

Cl

H

H

CH(CH

3

)

2

6.058

CF

3

OCH

3

H

H

CH(CH

3

)

2

6.059

CF

3

CH

3

H

H

CH(CH

3

)

2

6.06

H

CF

3

H

CH

3

CH(CH

3

)

2

6.061

H

CF

3

H

CF

3

CH(CH

3

)

2

6.062

H

CF

3

H

SCH

3

CH(CH

3

)

2

6.063

H

CF

3

H

SOCH

3

CH(CH

3

)

2

6.064

H

CF

3

H

SO

2

CH

3

CH(CH

3

)

2

6.065

H

CF

3

H

Cl

CH(CH

3

)

2

6.066

H

CF

3

H

OCH

3

CH(CH

3

)

2

6.067

H

CH

3

H

CF

3

CH(CH

3

)

2

6.068

H

Cl

H

CF

3

CH(CH

3

)

2

6.069

H

OCH

3

H

CF

3

CH(CH

3

)

2

6.07

CN

CF

3

H

H

CH(CH

3

)

2

6.071

Cl

CF

3

H

H

HNPh

6.072

CHF

2

CF

3

H

H

HNPh

6.073

CCl

3

CF

3

H

H

HNPh

6.074

CClF

2

CF

3

H

H

HNPh

6.075

CF

3

CF

3

H

H

HNPh

6.076

CH

3

CF

3

H

H

HNPh

6.077

CH

2

CH

3

CF

3

H

H

HNPh

6.078

(CH

2

)

2

CH

3

CF

3

H

H

HNPh

6.079

CH

2

F

CF

3

H

H

HNPh

6.08

CH

2

Cl

CF

3

H

H

HNPh

6.081

CH

2

OCH

3

CF

3

H

H

HNPh

6.082

CH

2

SMe

CF

3

H

H

HNPh

6.083

CH

2

SO

2

Me

CF

3

H

H

HNPh

6.084

CH═CH

2

CF

3

H

H

HNPh

6.085

CH

2

CH═CH

2

CF

3

H

H

HNPh

6.086

CCH

CF

3

H

H

HNPh

6.087

CF

3

SCH

3

H

H

HNPh

6.088

CF

3

SOCH

3

H

H

HNPh

6.089

CF

3

SO

2

CH

3

H

H

HNPh

6.09

CF

3

OCH

3

H

H

HNPh

6.091

CF

3

CN

H

H

HNPh

6.092

CF

3

Cl

H

H

HNPh

6.093

CF

3

OCH

3

H

H

HNPh

6.094

CF

3

CH

3

H

H

HNPh

6.095

H

CF

3

H

CH

3

HNPh

6.096

H

CF

3

H

CF

3

HNPh

6.097

H

CF

3

H

SCH

3

HNPh

6.098

H

CF

3

H

SOCH

3

HNPh

6.099

H

CF

3

H

SO

2

CH

3

HNPh

6.1

H

CF

3

H

Cl

HNPh

6.101

H

CF

3

H

OCH

3

HNPh

6.102

H

CH

3

H

CF

3

HNPh

6.103

H

Cl

H

CF

3

HNPh

6.104

H

OCH

3

H

CF

3

HNPh

6.105

CN

CF

3

H

H

HNPh

6.106

Cl

CF

3

H

H

HNC(CH

3

)

3

6.107

CHF

2

CF

3

H

H

HNC(CH

3

)

3

6.108

CCl

3

CF

3

H

H

HNC(CH

3

)

3

6.109

CClF

2

CF

3

H

H

HNC(CH

3

)

3

6.11

CF

3

CF

3

H

H

HNC(CH

3

)

3

6.111

CH

3

CF

3

H

H

HNC(CH

3

)

3

6.112

CH

2

CH

3

CF

3

H

H

HNC(CH

3

)

3

6.113

(CH

2

)

2

CH

3

CF

3

H

H

HNC(CH

3

)

3

6.114

CH

2

F

CF

3

H

H

HNC(CH

3

)

3

6.115

CH

2

Cl

CF

3

H

H

HNC(CH

3

)

3

6.116

CH

2

OCH

3

CF

3

H

H

HNC(CH

3

)

3

6.117

CH

2

SMe

CF

3

H

H

HNC(CH

3

)

3

6.118

CH

2

SO

2

Me

CF

3

H

H

HNC(CH

3

)

3

6.119

CH═CH

2

CF

3

H

H

HNC(CH

3

)

3

6.12

CH

2

CH═CH

2

CF

3

H

H

HNC(CH

3

)

3

6.121

CCH

CF

3

H

H

HNC(CH

3

)

3

6.122

CF

3

SCH

3

H

H

HNC(CH

3

)

3

6.123

CF

3

SOCH

3

H

H

HNC(CH

3

)

3

6.124

CF

3

SO

2

CH

3

H

H

HNC(CH

3

)

3

6.125

CF

3

OCH

3

H

H

HNC(CH

3

)

3

6.126

CF

3

CN

H

H

HNC(CH

3

)

3

6.127

CF

3

Cl

H

H

HNC(CH

3

)

3

6.128

CF

3

OCH

3

H

H

HNC(CH

3

)

3

6.129

CF

3

CH

3

H

H

HNC(CH

3

)

3

6.13

H

CF

3

H

CH

3

HNC(CH

3

)

3

6.131

H

CF

3

H

CF

3

HNC(CH

3

)

3

6.132

H

CF

3

H

SCH

3

HNC(CH

3

)

3

6.133

H

CF

3

H

SOCH

3

HNC(CH

3

)

3

6.134

H

CF

3

H

SO

2

CH

3

HNC(CH

3

)

3

6.135

H

CF

3

H

Cl

HNC(CH

3

)

3

6.136

H

CF

3

H

OCH

3

HNC(CH

3

)

3

6.137

H

CH

3

H

CF

3

HNC(CH

3

)

3

6.138

H

Cl

H

CF

3

HNC(CH

3

)

3

6.139

H

OCH

3

H

CF

3

HNC(CH

3

)

3

6.14

CN

CF

3

H

H

HNC(CH

3

)

3

TABLE 7

Comp. No.

R

1

R

2

R

3

R

4

p

7.001

H

CF

3

H

H

0

7.002

F

CF

3

H

H

0

7.003

Cl

CF

3

H

H

0

7.004

Br

CF

3

H

H

0

7.005

CHF

2

CF

3

H

H

0

7.006

CCl

3

CF

3

H

H

0

7.007

CClF

2

CF

3

H

H

0

7.008

CF

3

CF

3

H

H

0

7.009

CH

3

CF

3

H

H

0

7.01

CH

2

CH

3

CF

3

H

H

0

7.011

CH(CH

3

)

2

CF

3

H

H

0

7.012

(CH

2

)

2

CH

3

CF

3

H

H

0

7.013

C(CH

3

)

3

CF

3

H

H

0

7.014

Ph

CF

3

H

H

0

7.015

CH

2

F

CF

3

H

H

0

7.016

CH

2

Cl

CF

3

H

H

0

7.017

CH

2

Br

CF

3

H

H

0

7.018

CH

2

OH

CF

3

H

H

0

7.019

CH

2

OCOCH

3

CF

3

H

H

0

7.02

CH

2

OCOPh

CF

3

H

H

0

7.021

CH

2

OCH

3

CF

3

H

H

0

7.022

CH

2

OCH

2

CH

3

CF

3

H

H

0

7.023

CH

2

CH

2

OCH

3

CF

3

H

H

0

7.024

CH

2

SMe

CF

3

H

H

0

7.025

CH

2

SOMe

CF

3

H

H

0

7.026

CH

2

SO

2

Me

CF

3

H

H

0

7.027

CH

2

SO

2

Ph

CF

3

H

H

0

7.028

SCH

3

CF

3

H

H

0

7.029

SOCH

3

CF

3

H

H

0

7.03

SO

2

CH

3

CF

3

H

H

0

7.031

N(CH

3

)

2

CF

3

H

H

0

7.032

CH═CH

2

CF

3

H

H

0

7.033

CH

2

CH═CH

2

CF

3

H

H

0

7.034

SO

2

N(CH

3

)

2

CF

3

H

H

0

7.035

CCH

CF

3

H

H

0

7.036

cyclopropyl

CF

3

H

H

0

7.037

OCH

3

CF

3

H

H

0

7.038

OCHF

2

CF

3

H

H

0

7.039

OCH

2

CCH

CF

3

H

H

0

7.04

H

CF

2

CF

3

H

H

0

7.041

Cl

CF

2

CF

3

H

H

0

7.042

CHF

2

CF

2

CF

3

H

H

0

7.043

CCl

3

CF

2

CF

3

H

H

0

7.044

CClF

2

CF

2

CF

3

H

H

0

7.045

CF

3

CF

2

CF

3

H

H

0

7.046

CH

3

CF

2

CF

3

H

H

0

7.047

CH

2

CH

3

CF

2

CF

3

H

H

0

7.048

CH(CH

3

)

2

CF

2

CF

3

H

H

0

7.049

(CH

2

)

2

CH

3

CF

2

CF

3

H

H

0

7.05

C(CH

3

)

3

CF

2

CF

3

H

H

0

7.051

CH

2

F

CF

2

CF

3

H

H

0

7.052

CH

2

Cl

CF

2

CF

3

H

H

0

7.053

CH

2

OH

CF

2

CF

3

H

H

0

7.054

CH

2

OCOCH

3

CF

2

CF

3

H

H

0

7.055

CH

2

OCOPh

CF

2

CF

3

H

H

0

7.056

CH

2

OCH

3

CF

2

CF

3

H

H

0

7.057

CH

2

OCH

2

CH

3

CF

2

CF

3

H

H

0

7.058

CH

2

SMe

CF

2

CF

3

H

H

0

7.059

CH

2

SOMe

CF

2

CF

3

H

H

0

7.06

CH

2

SO

2

Me

CF

2

CF

3

H

H

0

7.061

CH

2

SO

2

Ph

CF

2

CF

3

H

H

0

7.062

N(CH

3

)

2

CF

2

CF

3

H

H

0

7.063

CH═CH

2

CF

2

CF

3

H

H

0

7.064

CH

2

CH═CH

2

CF

2

CF

3

H

H

0

7.065

SO

2

N(CH

3

)

2

CF

2

CF

3

H

H

0

7.066

CCH

CF

2

CF

3

H

H

0

7.067

cyclopropyl

CF

2

CF

3

H

H

0

7.068

OCH

3

CF

2

CF

3

H

H

0

7.069

CO

2

Me

CF

2

CF

3

H

H

0

7.07

OCH

2

CCH

CF

2

CF

3

H

H

0

7.071

H

CF

2

Cl

H

H

0

7.072

Cl

CF

2

Cl

H

H

0

7.073

CHF

2

CF

2

Cl

H

H

0

7.074

CCl

3

CF

2

Cl

H

H

0

7.075

CClF

2

CF

2

Cl

H

H

0

7.076

CF

3

CF

2

Cl

H

H

0

7.077

CH

3

CF

2

Cl

H

H

0

7.078

CH

2

CH

3

CF

2

Cl

H

H

0

7.079

CH(CH

3

)

2

CF

2

Cl

H

H

0

7.08

(CH

2

)

2

CH

3

CF

2

Cl

H

H

0

7.081

C(CH

3

)

3

CF

2

Cl

H

H

0

7.082

CH

2

F

CF

2

Cl

H

H

0

7.083

CH

2

Cl

CF

2

Cl

H

H

0

7.084

CH

2

OH

CF

2

Cl

H

H

0

7.085

CH

2

OCOCH

3

CF

2

Cl

H

H

0

7.086

CH

2

OCOPh

CF

2

Cl

H

H

0

7.087

CH

2

OCH

3

CF

2

Cl

H

H

0

7.088

CH

2

OCH

2

CH

3

CF

2

Cl

H

H

0

7.089

CH

2

SMe

CF

2

Cl

H

H

0

7.09

CH

2

SOMe

CF

2

Cl

H

H

0

7.091

CH

2

SO

2

Me

CF

2

Cl

H

H

0

7.092

CH

2

SO

2

Ph

CF

2

Cl

H

H

0

7.093

N(CH

3

)

2

CF

2

Cl

H

H

0

7.094

CH═CH

2

CF

2

Cl

H

H

0

7.095

CH

2

CH═CH

2

CF

2

Cl

H

H

0

7.096

SO

2

N(CH

3

)

2

CF

2

Cl

H

H

0

7.097

CCH

CF

2

Cl

H

H

0

7.098

cyclopropyl

CF

2

Cl

H

H

0

7.099

OCH

3

CF

2

Cl

H

H

0

7.1

OCH

2

CCH

CF

2

Cl

H

H

0

7.101

CF

3

CHF

2

H

H

0

7.102

CH

3

CHF

2

H

H

0

7.103

CH

2

OCH

3

CHF

2

H

H

0

7.104

CH

2

Cl

CHF

2

H

H

0

7.105

CH

2

F

CHF

2

H

H

0

7.106

CH

3

CF

3

H

CH

3

0

7.107

Cl

CF

3

H

CH

3

0

7.108

CH

3

CF

3

CH

3

H

0

7.109

CH

3

CF

3

Cl

H

0

7.11

OCH

3

CF

3

CH

3

H

0

7.111

CH

2

OCH

3

CF

3

CH

3

H

0

7.112

CH

2

OCH

3

CF

3

Cl

H

0

7.113

COOCH

3

H

H

H

0

7.114

CF

3

SCH

3

H

H

0

7.115

CH

3

SCH

3

H

H

0

7.116

CF

3

SOCH

3

H

H

0

7.117

CH

3

SOCH

3

H

H

0

7.118

CF

3

SO

2

CH

3

H

H

0

7.119

CH

3

SO

2

CH

3

H

H

0

7.12

CF

3

OCH

3

H

H

0

7.121

CH

3

OCH

3

H

H

0

7.122

CF

3

OCH

2

CF

3

H

H

0

7.123

CH

3

OCH

2

CF

3

H

H

0

7.124

CF

3

OCH

2

CCH

H

H

0

7.125

CH

3

OCH

2

CCH

H

H

0

7.126

CF

3

CN

H

H

0

7.127

CH

3

CN

H

H

0

7.128

CF

3

Cl

H

H

0

7.129

CF

3

Cl

H

H

0

7.13

CH

3

Cl

H

H

0

7.131

H

Cl

H

H

0

7.132

CF

3

OCH

3

H

H

0

7.133

CH

3

OCH

3

H

H

0

7.134

CF

3

CH

3

H

H

0

7.135

H

CF

3

H

CH

3

0

7.136

H

CF

3

H

CF

3

0

7.137

H

CF

3

H

CH

2

CH

3

0

7.138

H

CF

3

H

CF

3

0

7.139

H

CF

3

H

SCH

3

0

7.14

H

CF

3

H

SOCH

3

0

7.141

H

CF

3

H

SO

2

CH

3

0

7.142

H

CF

3

H

Cl

0

7.143

H

CF

3

H

OCH

3

0

7.144

H

CH

3

H

CF

3

0

7.145

H

Cl

H

CF

3

0

7.146

H

OCH

3

H

CF

3

0

7.147

H

SCH

3

H

CF

3

0

7.148

H

SOCH

3

H

CF

3

0

7.149

CH

3

(CF

2

)

3

CF

3

H

H

0

7.15

CF

2

H

SCH

3

H

H

0

7.151

CF

2

Cl

SCH

3

H

H

0

7.152

CF

2

H

SOCH

3

H

H

0

7.153

CF

2

Cl

SOCH

3

H

H

0

7.154

CF

2

H

SO

2

CH

3

H

H

0

7.155

CF

2

Cl

SO

2

CH

3

H

H

0

7.156

CF

2

H

OCH

3

H

H

0

7.157

CF

2

Cl

OCH

3

H

H

0

7.158

CF

2

H

OCH

2

CF

3

H

H

0

7.159

CF

2

Cl

OCH

2

CF

3

H

H

0

7.16

CF

2

H

OCH

2

CCH

H

H

0

7.161

CF

2

Cl

OCH

2

CCH

H

H

0

7.162

CF

2

H

CN

H

H

0

7.163

CF

2

Cl

CN

H

H

0

7.164

CF

2

H

Cl

H

H

0

7.165

CF

2

Cl

Cl

H

H

0

7.166

CF

2

H

OCH

3

H

H

0

7.167

CF

2

Cl

OCH

3

H

H

0

7.168

CF

3

CH

2

OCH

3

H

H

0

7.169

CF

2

Cl

CH

2

OCH

3

H

H

0

7.17

CF

2

H

CH

2

OCH

3

H

H

0

7.171

CN

CF

3

H

H

0

7.172

H

CF

3

H

H

2

7.173

F

CF

3

H

H

2

7.174

Cl

CF

3

H

H

2

7.175

Br

CF

3

H

H

2

7.176

CHF

2

CF

3

H

H

2

7.177

CCl

3

CF

3

H

H

2

7.178

CClF

2

CF

3

H

H

2

7.179

CF

3

CF

3

H

H

2

7.18

CH

3

CF

3

H

H

2

7.181

CH

2

CH

3

CF

3

H

H

2

7.182

CH(CH

3

)

2

CF

3

H

H

2

7.183

(CH

2

)

2

CH

3

CF

3

H

H

2

7.184

C(CH

3

)

3

CF

3

H

H

2

7.185

Ph

CF

3

H

H

2

7.186

CH

2

F

CF

3

H

H

2

7.187

CH

2

Cl

CF

3

H

H

2

7.188

CH

2

Br

CF

3

H

H

2

7.189

CH

2

OH

CF

3

H

H

2

7.19

CH

2

OCOCH

3

CF

3

H

H

2

7.191

CH

2

OCOPh

CF

3

H

H

2

7.192

CH

2

OCH

3

CF

3

H

H

2

7.193

CH

2

OCH

2

CH

3

CF

3

H

H

2

7.194

CH

2

CH

2

OCH

3

CF

3

H

H

2

7.195

CH

2

SMe

CF

3

H

H

2

7.196

CH

2

SOMe

CF

3

H

H

2

7.197

CH

2

SO

2

Me

CF

3

H

H

2

7.198

CH

2

SO

2

Ph

CF

3

H

H

2

7.199

SCH

3

CF

3

H

H

2

7.2

SOCH

3

CF

3

H

H

2

7.201

SO

2

CH

3

CF

3

H

H

2

7.202

N(CH

3

)

2

CF

3

H

H

2

7.203

CH═CH

2

CF

3

H

H

2

7.204

CH

2

CH═CH

2

CF

3

H

H

2

7.205

SO

2

N(CH

3

)

2

CF

3

H

H

2

7.206

CCH

CF

3

H

H

2

7.207

cyclopropyl

CF

3

H

H

2

7.208

OCH

3

CF

3

H

H

2

7.209

OCHF

2

CF

3

H

H

2

7.21

OCH

2

CCH

CF

3

H

H

2

TABLE 8

Comp. No.

R

1

R

2

R

3

R

4

8.001

H

CF

3

H

H

8.002

F

CF

3

H

H

8.003

Cl

CF

3

H

H

8.004

Br

CF

3

H

H

8.005

CHF

2

CF

3

H

H

8.006

CCl

3

CF

3

H

H

8.007

CClF

2

CF

3

H

H

8.008

CF

3

CF

3

H

H

8.009

CH

3

CF

3

H

H

8.01

CH

2

CH

3

CF

3

H

H

8.011

CH(CH

3

)

2

CF

3

H

H

8.012

(CH

2

)

2

CH

3

CF

3

H

H

8.013

C(CH

3

)

3

CF

3

H

H

8.014

Ph

CF

3

H

H

8.015

CH

2

F

CF

3

H

H

8.016

CH

2

Cl

CF

3

H

H

8.017

CH

2

Br

CF

3

H

H

8.018

CH

2

OH

CF

3

H

H

8.019

CH

2

OCOCH

3

CF

3

H

H

8.02

CH

2

OCOPh

CF

3

H

H

8.021

CH

2

OCH

3

CF

3

H

H

8.022

CH

2

OCH

2

CH

3

CF

3

H

H

8.023

CH

2

CH

2

OCH

3

CF

3

H

H

8.024

CH

2

SMe

CF

3

H

H

8.025

CH

2

SOMe

CF

3

H

H

8.026

CH

2

SO

2

Me

CF

3

H

H

8.027

CH

2

SO

2

Ph

CF

3

H

H

8.028

SCH

3

CF

3

H

H

8.029

SOCH

3

CF

3

H

H

8.03

SO

2

CH

3

CF

3

H

H

8.031

N(CH

3

)

2

CF

3

H

H

8.032

CH═CH

2

CF

3

H

H

8.033

CH

2

CH═CH

2

CF

3

H

H

8.034

SO

2

N(CH

3

)

2

CF

3

H

H

8.035

CCH

CF

3

H

H

8.036

cyclopropyl

CF

3

H

H

8.037

OCH

3

CF

3

H

H

8.038

OCHF

2

CF

3

H

H

8.039

OCH

2

CCH

CF

3

H

H

TABLE 9

Comp. No.

R

1

R

2

R

3

R

4

9.001

H

CF

3

H

H

9.002

F

CF

3

H

H

9.003

Cl

CF

3

H

H

9.004

Br

CF

3

H

H

9.005

CHF

2

CF

3

H

H

9.006

CCl

3

CF

3

H

H

9.007

CClF

2

CF

3

H

H

9.008

CF

3

CF

3

H

H

9.009

CH

3

CF

3

H

H

9.01

CH

2

CH

3

CF

3

H

H

9.011

CH(CH

3

)

2

CF

3

H

H

9.012

(CH

2

)

2

CH

3

CF

3

H

H

9.013

C(CH

3

)

3

CF

3

H

H

9.014

Ph

CF

3

H

H

9.015

CH

2

F

CF

3

H

H

9.016

CH

2

Cl

CF

3

H

H

9.017

CH

2

Br

CF

3

H

H

9.018

CH

2

OH

CF

3

H

H

9.019

CH

2

OCOCH

3

CF

3

H

H

9.02

CH

2

OCOPh

CF

3

H

H

9.021

CH

2

OCH

3

CF

3

H

H

9.022

CH

2

OCH

2

CH

3

CF

3

H

H

9.023

CH

2

CH

2

OCH

3

CF

3

H

H

9.024

CH

2

SMe

CF

3

H

H

9.025

CH

2

SOMe

CF

3

H

H

9.026

CH

2

SO

2

Me

CF

3

H

H

9.027

CH

2

SO

2

Ph

CF

3

H

H

9.028

SCH

3

CF

3

H

H

9.029

SOCH

3

CF

3

H

H

9.03

SO

2

CH

3

CF

3

H

H

9.031

N(CH

3

)

2

CF

3

H

H

9.032

CH═CH

2

CF

3

H

H

9.033

CH

2

CH═CH

2

CF

3

H

H

9.034

SO

2

N(CH

3

)

2

CF

3

H

H

9.035

CCH

CF

3

H

H

9.036

cyclopropyl

CF

3

H

H

9.037

OCH

3

CF

3

H

H

9.038

OCHF

2

CF

3

H

H

9.039

OCH

2

CCH

CF

3

H

H

Physical data (melting points in ° C.):

Comp.

No.

1.001

resin

1.005

crystals m.p. 61-62

1.008

oil

1.009

crystals m.p. 75-77

1.01

oil

1.011

crystals m.p. 111-112

1.012

crystals m.p. 87-88

1.013

crystals m.p. 112-114

1.014

oil

1.021

crystals m.p. 128-129

1.023

crystals m.p. 91-92

1.024

oil

1.026

amorphous

1.028

amorphous

1.03

resin

1.031

crystals m.p. 145-146

1.042

oil

1.043

crystals m.p. 107-110

1.047

crystals m.p. 155-156

1.048

viscous

1.05

crystals m.p. 51-53

1.06

crystals m.p. >220

1.109

oil

1.195

oil

1.258

crystals m.p. 119-121

1.31

crystals m.p. 92-94

1.312

viscous

1.313

crystals m.p. 137-138

1.314

oil

1.316

resin

1.323

oil

1.334

resin

1.335

crystals m.p. 140-142

1.339

crystals m.p. 137-139

1.341

resin

1.343

crystals m.p. 97-99

1.347

crystals m.p. 135-137

1.349

oil, n

D

1.4965

1.351

crystals m.p. 125-127

1.353

resin, n

D

1.5289

1.355

crystals m.p. 90-92

1.356

resin

1.358

resin

1.361

oil

1.362

crystals m.p. 139-142

1.371

crystals m.p. 96-97

1.372

resin

1.373

resin

1.374

crystals m.p. 116-1199

1.375

resin

1.376

crystals m.p. >270

1.381

crystals m.p. 117-118

1.383

crystals m.p. 172-173

1.384

resin

1.385

resin

1.386

resin

1.387

resin

1.388

crystals m.p. 102-104

1.389

crystals m.p. 143-145

1.39

crystals m.p. 195-197

1.391

solid

1.392

crystals m.p. 202-206

1.398

crystals m.p. 137-138

1.399

crystals m.p. 262-263

1.4

oil

1.401

oil

1.402

oil

1.403

oil

1.404

oil

1.405

viscous

1.406

oil

1.408

oil

1.409

oil

1.41

oil

1.411

crystals m.p. 98-100

1.412

crystals m.p. 130-131

1.413

crystals m.p. 167-170

1.414

crystals m.p. 166-167

1.415

crystals m.p. 91-93

1.418

crystals m.p. 149-150

1.421

crystals m.p. 88-89

1.422

crystals m.p. 175-177

1.423

crystals m.p. 45-47

1.424

crystals m.p. 102-104

2.001

resin

2.003

oil

2.03

crystals m.p. 107-110

2.038

crystals m.p. 111-113

2.043

resin

2.044

crystals m.p. 105-106

2.045

amorphous

3.001

crystals m.p. 95-97

3.054

oil

3.055

crystals m.p. 108-110

3.056

resin, D

D

1.5509

4.009

crystals m.p. 107-109

4.01

oil

4.011

oil

4.014

crystals m.p. 148-149

4.021

crystals m.p. 44-45

4.033

crystals m.p. 46-48

4.124

crystals m.p. 46-48

4.328

oil

5.008

resin

5.081

resin

5.083

crystals m.p. 161-162

5.084

crystals m.p. 215-216

5.085

resin

6.006

crystals m.p. 176-177

6.041

crystals m.p. 186-187

6.076

crystals m.p. 195-196

6.111

crystals m.p. 163-164

7.009

ratio A: B = 2:1. H-NMR(CDCl

3

,ppm) SCH

3

: A: 2.50; B: 2.66.

7.01

ratio A: B = 5:1. H-NMR(CDCl

3

,ppm) SCH

3

: A: 2.50; B: 2.64.

7.011

ratio A: B = 9:1. H-NMR(CDCl

3

,ppm) SCH

3

: A: 2.46; B: 2.59.

7.021

ratio A: B = 3:1. H-NMR(CDCl

3

,ppm) SCH

3

: A: 2.50; B: 2.62.

7.18

ratio A: B = 2:. H-NMR(CDCl

3

,ppm) SO

2

CH

3

: A: 3.40;

B: 3.58.

7.182

ratio A: B = 9:1. H-NMR(CDCl

3

,ppm) SO

2

CH

3

: A: 3.32;

B: 3.50.

7.192

ratio A: B = 3:1. H-NMR(CDCl

3

,ppm) SO

2

CH

3

: A: 3.40;

B: 3.58.

8.009

crystals m.p. 96-97

8.01

amorphous

8.011

oil

8.021

oil

9.009

crystals m.p. 112-113

9.01

amorphous

9.011

amorphous

9.021

oil

Biological Examples

Example B1

Herbical action before emergence of the plants (pre-emergence action)

Monocotyledonous and dicotyledonous test plants are sown in standard soil in plastic pots. Immediately after sowing, the test substances are sprayed on (500 l of water/ha) as an aqueous suspension (prepared from a 25% wettable powder (Example F3, b) according to WO 97/34485) or emulsion (prepared from a 25% emulsion concentrate (Example F1, c)), corresponding to a dosage of 2 kg of AS/ha. The test plants are then grown under optimum conditions in a greenhouse. After a test period of 3 weeks, the test is evaluated with a nine-level scale of ratings (1=complete damage, 9=no effect). Ratings of 1 to 4 (in particular 1 to 3) mean good to very good herbicidal action.

TABLE B1

pre-emergence action:

Active

compound

Test plant

No.

Avena

Cyperus

Setaria

Sinapis

Solanum

Stellaria

1.009

2

1

1

2

1

2

1.376

2

1

1

2

1

2

4.009

1

2

1

2

1

3

7.009

4

2

1

3

1

2

1.381

4

1

2

2

1

1

1.011

2

1

1

1

1

1

5.008

2

1

1

2

1

2

4.021

2

1

2

2

1

2

1.010

2

1

1

1

1

2

1.021

4

2

1

1

1

3

1.398

2

1

1

1

1

1

1.195

2

1

1

1

1

2

4.124

2

1

2

2

1

2

1.411

3

2

1

2

1

2

1.042

4

2

2

1

1

4

1.023

2

2

2

1

1

2

1.109

2

2

2

2

1

3

1.313

3

1

2

1

1

2

1.401

2

1

1

2

1

2

1.404

2

1

1

2

1

2

1.400

2

1

1

2

1

2

1.403

2

1

1

1

1

2

1.405

2

1

1

1

1

2

1.406

2

1

1

1

1

2

1.402

2

1

1

2

1

2

1.005

4

1

1

1

1

1

1.043

4

2

1

2

1

2

1.409

1

1

1

1

1

1

1.41

2

1

1

1

1

1

1.06

2

1

1

2

1

1

7.192

4

2

2

3

2

2

7.021

1

1

1

1

1

1

The same results are obtained when the compounds of the formula I are formulated according to Examples F2 and F4 to F8 according to WO 97/34485.

Example B2

Post-emeroence Herbicidal Action

Monocotyledonous and dicotyledonous test plants are grown in plastic pots with standard soil in a greenhouse and, in the 4- to 6-leaf stage, are sprayed with an aqueous suspension of the test substances of the formula 1, prepared from a 25% wettable powder (Example F3, b) according to WO 97134485) or with an emulsion of the test substances of the formula I, prepared from a 25% emulsion concentrate (Example F1, c) according to WO 97/34485), corresponding to a dosage of 2 kg of AS/ha (500 l of water/ha). The test plants are then grown further under optimum conditions in a greenhouse. After a test period of about 18 days, the test is evaluated with a nine-level scale of rating (1=complete damage, 9=no effect). Ratings of 1 to 4 (in particular 1 to 3) mean good to very good herbicidal action. In this test, the compounds of the formula I show strong herbicidal action.

TABLE B2

post-emergence action:

Active compound

Test plant

No.

Avena

Setaria

Solanum

Sinapis

Stellaria

1.009

1

1

1

1

2

1.376

1

2

2

1

2

4.009

1

1

1

1

1

1.026

3

1

1

1

2

7.009

3

2

1

1

1

1.381

2

2

2

2

2

1.011

2

2

2

2

2

5.008

2

3

1

1

2

5.085

3

2

2

1

2

4.021

2

2

1

1

2

1.012

3

2

2

1

2

1.010

2

2

2

1

4

4.010

3

3

2

2

2

1.021

2

4

2

1

2

1.398

2

2

2

1

2

1.195

2

2

2

1

2

4.124

2

2

1

1

2

1.411

2

2

2

1

2

1.008

2

2

2

1

2

6.006

2

5

2

2

2

5.081

3

2

1

1

2

1.042

2

2

2

1

2

1.023

2

2

2

1

2

1.109

2

2

2

1

2

1.313

2

2

2

1

2

1.401

2

2

2

2

2

1.404

2

2

1

1

2

1.400

2

2

2

1

2

1.403

2

2

2

1

2

1.403

2

2

2

1

2

1.405

2

2

2

1

2

1.406

2

2

1

1

2

1.402

2

2

2

1

2

1.001

3

2

2

1

2

1.005

2

2

2

1

2

1.362

3

2

2

1

2

1.043

2

2

2

1

2

1.409

2

1

1

1

2

1.410

1

1

1

1

1

1.060

2

1

1

1

2

7.192

2

3

3

2

2

7.021

1

2

1

1

2

1.048

2

1

1

1

2

The same results are obtained when the compounds of the formula I are formulated according to Examples F2 and F4 to F8 according to WO 97/34485.

Example B3

Herbicidal action before emergence of the plants (pre-emergence action)

Monocotyledonous and dicotyledonous test plants are sown in pots in standard soil. Immediately after sowing, the test substances are sprayed on (500 l of spray liquorlha) as an aqueous suspension, prepared from a wettable powder WP10 corresponding to the desired dosage (250 g of a.i./ha).

The test plants are then grown under optimum conditions in a greenhouse. After a test period of 3 weeks, the test is evaluated with a nine -evel scale of ratings (1=complete damage, 9=no effect). Ratings of 1 to 4 (in particular 1 to 3) mean good to very good herbicidal action, 7-9 mean good tolerance.

TABLE B3

Pre-emergence action:

Test plant

Active

Dose

compound

Abut-

Amar-

Cheno-

[g of

No.

ilon

anthus

podium

Kochia

Sida

Stellaria

AS/ha]

1.355

1

1

1

1

2

2

250

1.347

2

2

1

1

4

1

250

1.335

1

2

1

5

2

7

250

1.349

1

3

1

4

2

5

250

1.339

2

1

1

7

2

1

250

1.341

3

9

1

9

4

1

250

1.343

1

4

1

9

3

5

250

The same results are obtained when the compounds of the formula I are formulated according to Examples F2 and F4 to F8 according to WO 97/34485.

Example B4

Herbicidal action after the emergence of the plants ( post-emer gence action)

Monocotyledonous and dicotyledonous test plants are sown in pots in standard soil. In the 2-3- leaf stage of the test plants, the test substances are sprayed on (500 l of spray liquor/ha) as an aqueous suspension, prepared from a wettable powder WP10 according to the desired dosage (250 g of a.i./ha). 0.2% of X77 is added as wetting agent to the spray liquor. The test plants are then grown under optimum conditions in a greenhouse.

After a test period of 3 weeks, the test is evaluated with a nine4evel scale of ratings (1=complete damage, 9=no effect). Ratings of 1 to 4 (in particular 1 to 3) mean good to very good herbicidal action, 7-9 mean good tolerance.

TABLE B4

Post-emergence action:

Test plant

Active

Dose

compound

Abut-

Amar-

Cheno-

[g of

No.

ilon

anthus

podium

Kochia

Sida

Stellaria

AS/ha]

1.355

2

2

2

3

2

3

250

1.347

3

2

2

2

3

3

250

1.335

3

2

2

2

2

3

250

1.349

2

2

2

2

2

3

250

1.339

2

2

3

1

4

3

250

1.351

5

2

3

3

3

3

250

1.341

5

2

3

4

5

4

250

1.343

3

2

2

3

9

3

250

1.361

2

2

2

2

2

3

250

The same results are obtained when the compounds of the formula I are formulated according to Examples F2 and F4 to F8 according to WO 97/34485.

Claims

1. A compound of the formula I in whicheach R independently is C1-C6alkyl, C1-C6alkenyl, C2-C6haloalkenyl, C2-C6alkynyl, C2-C6 haloalkynyl, C3-C6cycloalkyl, C1-C6alkoxy, C1-C6haloalkoxy, C1-C6alkylthio, C1-C6alkylsulfinyl, C1-C6alkylsulfonyl, C1-C6haloalkyl, C1-C6haloalkylthio, C1-C6haloalkylsulfinyl, C1-C6haloalkylsulfonyl, C1-C6alkoxycarbonyl, C1-C6alkylcarbonyl, C1-C6alkylamino, di-C1-C6 alkylamino, C1-C6alkylaminosulfonyl, di-C1-C6alkylaminosulfonyl, —N(R1)—S—R2, —N(R3)—SO—R4, —N(R5)—SO2—R6, nitro, cyano, halogen, hydroxyl, amino, formyl, hydroxy-C1-C6alkyl, C1-C6 alkoxy-C1-C6alkyl, C1-C6alkoxycarbonyloxy-C1-C6alkyl, C1-C6alkytthio-C1-C6alkyl, C1-C6 alkylsulfinyl-C1-C6alkyl, C1-C6alkylsulfonyl-C1-C6alkyl, thiocyanato-C1-C6alkyl, cyano-C1-C6 alkyl, oxiranyl, C3-C6alkenyloxy, C3-C6alkynyloxy, C1-C6alkoxy-C1-C6alkoxy, cyano-C1-C6 alkenyloxy, C1-C6alkoxycarbonyloxy-C1-C6alkoxy, C3-C6alkynyloxy, cyano-C1-C6lkoxy, C1-C6 alkoxycarbonyl-C1-C6alkoxy, C1-C6alkylthio-C1-C6alkoxy, alkoxycarbonyl-C1-C6alkylthio, alkoxycarbonyl-C1-C6alkylsulfinyl, alkoxycarbonyl-C1-C6alkylsulfonyl, C1-C6alkylsulfonyloxy, C1-C6haloalkylsulfonyloxy, phenyl, benzyl, phenoxy, phenylthio, phenylsulfinyl, phenylsulfonyl, benzylthio, benzylsulfinyl or benzylsulfonyl, where the phenyl groups may be mono- or polysubs ttuted by halogen, methyl, ethyl, trifluoromethyl, methoxy or nitro, or R is a five- to ten-membered monocyclic or fused bicyclic ring system, which may be aromatic or partially saturated and may contain 1 to 4 heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur, where the ring system is either attached directly to the pyridine ring or attached to the pyridine ring via a C1-C4alkylene group, and where each ring system may not contain more than 2 oxygen atoms and not more than two sulfur atoms, and where the ring system for its part may be mono-, di- or trisubstituted by C1-C6alkyl, C1-C6haloalkyl, C3-C6alkenyl, C3-C6haloalkenyl, C3-C6alkynyl, C3-C6haloalkynyl, C1-C6alkoxy, C1-C6 haloalkoxy, C3-C6alkenyloxy, C3-C6alkynyloxy, mercapto, C1-C6alkylthio, C1-C6haloalkylthio, C3-C6alkeny fthio, C3-C6haloalkenylthio, C3-C6alkynylthio, C2-C5alkoxyalkylthio, C3-C5acetylalkylthio, C3-C6alkoxycarbonylalky lthio, C2-C4cyanoalkylthio, C1-C6alkylsulfinyl, C1-C6 haloalkylsulfinyl, C1-C6alkylsulfonyl, C1-C6haloalkylsulfonyl, aminosulfonyl, C1-C2 alkylaminosulfonyl, C2-C4dialkylaminosulfonyl, C1-C3alkylene-R7, NR8R9, halogen, cyano, nitro, phenyl and benzylthio, where phenyl and benzylthio for their part may be substituted on the phenyl ring by C1-C3alkyl, C1-C3haloalkyl, C1-C3alkoxy, C1-C3haloalkoxy, halogen, cyano or nitro, and where substituents on the nitrogen in the heterocyclic ring are different from halogen; m is 1, 2,3 or 4; p is 0 or 1; R1, R3 and R5 independently of one another are hydrogen or C1-C6alkyl; R2 is NR10R11, C1-C6alkoxy, C1-C6haloalkoxy, C1-C6alkyl, C1-C6haloalkyl, C3-C6alkenyl, C3-C6 haloalkenyl, C3-C6alkynyl, C3-C6haloalkynyl, C3-C6cycloalkyl or phenyl, where phenyl for its part may be substituted by C1-C3alkyl, C1-C3haloalkyl, C1-C3alkoxy, C1-C3haloalkoxy, halogen, cyano or nitro; R4 is NR12R13, C1-C6alkoxy, C1-C6haloalkoxy, C1-C6alkyl, C1-C6haloalkyl, C3-C6alkenyl, C3-C6 haloalkenyl, C3-C6alkynyl, C3-C6haloalkynyl, C3-C6cycloalkyl or phenyl, where phenyl for its part may be substituted by C1-C3alkyl, C1-C3haloalkyl, C1-C3alkoxy, C1-C3haloalkoxy, halogen, cyano or nitro; R6is NR14R15, C1-C6alkoxy, C1-C6haloalkoxy, C1-C6alkyl, C1-C6haloalkyl, C3-C6alkenyl, C3-C8 haloalkenyl, C3-C6alkynyl, C3-C6haloalkynyl, C3-C6cycloalkyl or phenyl, where phenyl for its part may be substituted by C1-C3alkyl, C1-C3haloalkyl, C1-C3alkoxy, C1-C3haloalkoxy, halogen, cyano or nitro; R7 is C1-C3alkoxy, C2-C4alkoxycarbonyl, C1-C3alkylthio, C1-C3alkylsulfinyl, C1-C3alkylsulfonyl or phenyl, where phenyl for its part may be substituted by C1-C3alkyl, C1-C3haloalkyl, C1-C3 alkoxy, C1-C3haloalkoxy, halogen, cyano or nitro; R8, R10, R12 and R14 independently of one another are hydrogen or C1-C6alkyl; R9, R11, R13 and R15 independently of one another are C1-C6alkyl or C1-C6alkoxy; Q is the group Q1 in whichR16, R17, R18 and R19 independently of one another are hydrogen, hydroxyl, C1-C4alkyl, C2-C6 alkenyl, C2-C6alkynyl, C1-C4alkoxycarbonyl, C1-C6alkylthio, C1-C6alkylsulfinyl, C1-C6 alkylsulfonyl, C1-C4alkyl-NHS(O)2, C1-C4haloalkyl, —NH—C1-C4alkyl, —N(C1-C4alkyl)2, C1-C6 alkoxy, cyano, nitro, halogen or phenyl, which for its part may be substituted by C1-C4alkyl, C1-C4haloalkyl, C1-C4alkoxy, C1-C4haloalkoxy, C1-C4alkylcarbonyl, C1-C4alkoxycarbonyl, amino, C1-C4alkylamino, di-C1-C4alkylamino, C1-C6alkylthio, C1-C6alkylsulfinyl, C1-C6 alkylsulfonyl, C1-C4alkyl-S(O)2O, C1-C4haloalkylthio, C1-C4haloalkylsulfinyl, Cl-C4 haloalkylsulfonyl, C1-C4haloalkyl-S(O)2O, C1-C4aIkyl-S(O)2NH, C1-C4alkyl-S(O)2N(C1-C4 alkyl), halogen, nitro, COOH or cyano; or two adjacent substituents from the group consisting of R16, R17, R18 and R19 form a C2-C6alkylene bridge; R20 is hydroxyl, O−M+, halogen, cyano, SCN, OCN, C1-C12alkoxy, C1-C4alkoxycarbonyl-C1-C4 alkoxy, C1-C12alkylthio, C1-C12alkylsulfinyl, C1-C12alkylsulfonyl, C1-C12haloalkylthio, C1-C12 haloalkylsulfinyl, C1-C12haloalkylsulfonyl, C1-C6alkoxy-C1-C6alkylthio, C1-C6alkoxy-C1-C6 alkylsulfinyl, C1-C6alkoxy-C1-C6alkylsulfonyl, C2-C12alkenylthio, C2-C12alkenylsulfinyl, C2-C12 alkenylsulfonyl, C2-C12alkynylthio, C2-C12alkynylsulfinyl, C2-C12alkynylsulfonyl, C2-C12 haloalkenylthio, C2-C12haloalkenylsulfinyl, C2-C12haloalkenylsulfonyl, C1-C4alkoxycarbonyl-C1-C4alkylthio, C1-C4alkoxycarbonyl-C1-C4alkylsulfinyl, C1-C4alkoxycarbonyl-C1-C4alkylsulfonyl, (C1-C4alkoxy)2P(O)O, C1-C4alkyl-(C1-C4alkoxy)P(O)O, H(C1-C4alkoxy)P(O)O, R37R38N, R71R72NNH—, R21R22NC(O)O—, R73R74NC(O)NH—, C1-C4alkyl-S(O)2NR39, C1-C4 haloalkyl-S(O)2NR40, C1-C4alkyl-S(O)2O, C1-C4haloalkyl-S(O)2O, C1-C18alkylcarbonyloxy, where the alkyl group may be substituted by halogen, C1-C6alkoxy, C1-C6alkylthio or cyano, C2-C18alkenylcarbonyloxy, C2-C18alkynylcarbonyloxy, C3-C6cycloalkylcarbonyloxy, C1-C12 alkoxycarbonyloxy, C1-C12alkylthiocarbonyloxy, C1-C12alkylthiocarbamoyl, C1-C6alkyl-NH(CS)N(C1-C6alkyl)—NH—, di-C1-C6alkyl-N(CS)N(C1-C6alkyl)—NH—, benzyloxy, benzylthio, benzylsulfinyl, benzylsulfonyl, phenoxy, phenylthio, phenylsulfinyl, phenylsulfonyl, phenylsulfonyloxy or benzoyloxy, where the phenyl groups for their part may each be substituted by C1-C4alkyl, C1-C4haloalkyl, C1-C4alkoxy, C1-C4haloalkoxy, C1-C4alkylcarbonyl, C1-C4alkoxycarbonyl, C1-C4alkylamino, di-C1-C4alkylamino, C1-C4alkylthio, C1-C4alkylsulfinyl, C1-C4alkylsulfonyl, C1-C4alkyl-S(O)2O, C1-C4hatoalkylthio, C1-C4haloalkylsulfinyl, C1-C4 haloalkylsulfonyl, C1-C4haloalkyl-S(O)2O, C1-C4alkyl-S(O)2NH, C1-C4alkyl-S(O)2N(C1-C4 alkyl), halogen, nitro or cyano, or a group Ar1-thio, Ar2-sulfinyl, Ar3-sulfonyl, —OCO—Ar4 or NH—Ar5 in which Ar1, Ar2, Ar3, Ar4 and Ar5 independently of one another are a five- to ten-membered monocyclic or fused bicyclic ring system which may be aromatic or partially saturated and may contain 1 to 4 heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur, and in which each ring system may not contain more than 2 oxygen atoms and not more than two sulfur atoms, and in which the ring system for its part may be mono-, di- or trisubstituted by C1-C6alkyl, C1-C6haloalkyl, C3-C6alkenyl, C3-C6haloalkenyl, C3-C6alkynyl, C3-C6haloalkynyl, C1-C6alkoxy, C1-C6haloalkoxy, C3-C6alkenyloxy, C3-C6alkynyloxy, mercapto, C1-C6alkylthio, C1-C6haloalkylthio, C3-C6alkenylthio, C3--C6haloalkenylthio, C3-C6alkyny fthio, C2-C5 alkoxyalkylthio, C3-C5acetylalkylthio, C3-C6alkoxycarbonylalkylthio, C2-C4cyanoalkylthio, C1-C6alkylsulfinyl, C1-C6haloalkylsulfinyl, C1-C6alkylsulfonyl, C1-C6haloalkylsulfonyl, aminosulfonyl, C1-C2alkylaminosulfonyl, C2-C4dialkylaminosulfonyl, C1-C3alkylene-R41, NR42R43, halogen, cyano, nitro, phenyl and benzylthio, where phenyl and benzylthio for their part may be substituted on the phenyl ring by C1-C3alkyl, C1-C3haloalkyl, C1-C3alkoxy, C1-C3haloalkoxy, halogen, cyano or nitro, and where substituents on the nitrogen in the heterocyclic ring are different from halogen; R41 is C1-C3alkoxy, C2-C4alkoxycarbonyl , C1-C3alkylthio, C1-C3alkylsulfinyl, C1-C3 alkylsulfonyl or phenyl, where phenyl for its part may be substituted by C1-C3alkyl, C1-C3 haloalkyl, C1-C3alkoxy, C1-C3haloalkoxy, halogen, cyano or nitro; R42 is hydrogen or C1-C6alkyl; R43 is C1-C6alkyl or C1-C6alkoxy; R21, R37, R39, R40, R71 and R73 independently of one another are hydrogen or C1-C4alkyl; R22, R38, R72 and R74 independently of one another are hydrogen, C1-C12alkyl, hydroxyl, C1-C12alkoxy, C3-C6alkenyloxy or C3-C6alkynyloxy; or R21 and R22 together or R37 and R38 together or R71 and R72 together or R73 and R74 together are pyrrolidino, piperidino, morpholino, thiomorpholino, which may be mono- or polysubstituted by methyl groups; or are the group Q2 in whichY is a chemical bond, an alkylene group A l, carbonyl, oxygen, sulfur, sulfinyl, suifonyl, —NHR248 or NH(CO)R249; A1 is C(R246R247)m01; A is C(R244R245)r; r and m01 independently of one another are 1 or 2; R240 is hydrogen, methyl or C1-C3alkoxycarbonyl; R241, R242, R243, R244, R245, R246 and R247 independently of one another are hydrogen, halogen or methyl, or R243 together with an adjacent group R245 or R247 is a chemical bond; R248 and R249 independently of one another are hydrogen or C1-C4alkyl; R23 is hydroxyl, O−M+, halogen, cyano, SCN, OCN, C1-C12alkoxy, C1-C4alkoxycarbonyl-C1-C4 alkoxy, C1-C12alkylthio, C1-C12alkylsulfinyl, C1-C12alkylsulfonyl, C1-C12haloalkylthio, C1-C12 haloalkylsulfinyl, C1-C12haloalkylsulfonyl, C1-C6alkoxy-C1-C6alkylthio, C1-C6alkoxy-C1-C6 alkylsulfinyl, C1-C6alkoxy-C1-C6alkylsulfonyl, C2-C12alkenylthio, C2-C12alkenylsulfinyl, C2-C12 alkenylsulfonyl, C2-C12alkynylthio, C2-C12alkynylsulfinyl, C2-C12alkynylsulfonyl, C2-C12 haloalkenylthio, C2-C12haloalkenylsulfinyl, C2-C12haloalkenylsulfonyl, C1-C4alkoxycarbonyl-C1-C4alkylthio, C1-C4alkoxycarbonyl-C1-C4alkylsulfinyl, C1-C4alkoxycarbonyl-C1-C4alkylsulfonyl, (C1-C4alkoxy)2P(O)O, C1-C4alky l-(C1-C4alkoxy)P(O)O, H(C1-C4alkoxy)P(O)O, R44R45N, R75R76NNH—, R46R47NC(O)O—, R77R78NC(O)NH—, C1-C4alkyl-S(O)2NR48, C1-C4 haloalkyl-S(O)2NR49, C1-C4alkyl-S(O)2O, C1-C4haloalkyl-S(O)2O, C1-C18alkylcarbonyloxy, where the alkyl group may be substituted by halogen, C1-C6alkoxy, C1-C6alkylthio or cyano, C2-C18alkenylcarbonyloxy, C2-C18alkynylcarbonyloxy, C3-C6cycloalkylcarbonyioxy, C1-C12 alkoxycarbonyloxy, C1-C12alkylthiocarbonyloxy, C1-C12alkylthiocarbamoyl, C1-C6alkyl-NH(CS)N(C1-C6alkyl)—NH—, di-C1-C6alkyl-N(CS)N(C1-C6alkyl)—NH—, benzyloxy, benzylthio, benzyisulfinyl, benzylsulfonyl, phenoxy, phenylthio, phenylsulfinyl, phenylsulfonyl, phenylsulfonyloxy or benzoyloxy, where the phenyl groups for their part may each be substituted by C1-C4alkyl, C1-C4haloalkyl, C1-C4alkoxy, C1-C4haloalkoxy, C1-C4alkylcarbonyl, C1-C4alkoxycarbonyl, C1-C4alkylamino, di-C1-C4alkylamino, C1-C4alkylthio, C1-C4alkylsulfinyl, C1-C4alkylsulfonyl, C1-C4alkyl-S(O)2O, C1-C4haloalkylthio, C1-C4haloalkylsulfinyl, C1-C4 haloalkylsulfonyl, C1-C4haloalkyl-S(O)2O, C1-C4alkyl-S(O)2NH, C1-C4alkyl-S(O)2N(C1-C4 alkyl), halogen, nitro or cyano, or a group Ar6-thio, Arrsulfinyl, Ar8-sulfonyl, —OCO—Ar9 or NH—Ar10 in which Ar6, Ar7, Ar8, Ar9 and Ar10 independently of one another are a five- to ten-membered monocyclic or fused bicyclic ring system which may be aromatic or partially saturated and may contain 1 to 4 heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur, and in which each ring system may not contain more than 2 oxygen atoms and not more than two sulfur atoms, and in which the ring system for its part may be mono-, di- or trisubstituted by C1-C6alkyl, C1-C6haloalkyl, C3-C6alkenyl, C3-C6haloalkenyl, C3-C6alkynyl, C3-C6haloalkynyl, C1-C6alkoxy, C1-C6haloalkoxy, C3-C6alkenyloxy, C3-C6alkyny toxy, mercapto, C1-C6alkylthio, C1-C6haloalkylthio, C3-C6alkenylthio, C3-C6haloalkenylthio, C3-C6alkynylthio, C2-C5 alkoxyalkylthio, C3-C5acetylalkylthio, C3-C6alkoxycarbonylalkylthio, C2-C4cyanoalkylthio, C1-C6alkylsulfinyl, C1-C6haloalkylsulfinyl, C1-C6alkylsulfonyl, C1-C6haloalkylsulfonyl, aminosulfonyl, C1-C2alkylaminosulfonyl, C2-C4dialkylaminosulfonyl, C1-C3alkylene-R50, NR51R52, halogen, cyano, nitro, phenyl and benzylthio, where phenyl and benzylthio for their part may be substituted on the phenyl ring by C1-C3alkyl, C1-C3haloalkyl, C1-C3alkoxy, C1-C3haloalkoxy, halogen, cyano or nitro, and where substituents on the nitrogen in the heterocyclic ring are different from halogen; R50 is C1-C3alkoxy, C2-C4alkoxycarbonyl, C1-C3alkylthio, C1-C3alkylsulfinyl, C1-C3alkylsulfonyl or phenyl, where phenyl for its part may be substituted by C1-C3alkyl, C1-C3haloalkyl, C1-C3 alkoxy, C1-C3haloalkoxy, halogen, cyano or nitro; R51 is hydrogen or C1-C6alkyl; R52 is C1-C6alkyl or C1-C6alkoxy; R46, R44, R48, R49, R75 and R77 independently of one another are hydrogen or C1-C4alkyl; R47, R45, R76 and R78 independently of one another are hydrogen, C1-C12alkyl, hydroxyl, C1-C12alkoxy, C3-C6alkenyloxy or C3-C6alkynyloxy; or R44 and R45 together or R46 and R47 together or R75 and R76 together or R77 and R78 together are pyrro tidino, piperidino, morpholino, thiomorpholino, which may be mono- or polysubstituted by methyl groups; or are the group Q3 in whichR2 is hydroxyl, O−M+, halogen, cyano, SCN, OCN, C1-C12alkoxy, C1-C4alkoxycarbonyl-C1-C4 alkoxy, C1-C12alkylthio, C1-C12alkylsulfinyl, C1-C12alkylsulfonyl, C1-C12haloalkylthio, C1-C12 haloalkylsulfinyl, C1-C12haloalkylsulfonyl, C1-C6alkoxy-C1-C6alkylthio, C1-C6alkoxy-C1-C6 alkylsulfinyl, C1-C6alkoxy-C1-C6alkylsulfonyl, C2-C12alkenylthio, C2-C12alkenylsulfinyl, C2-C12 alkenylsulfonyl, C2-C12alkynylthio, C2-C12alkynylsulfinyl, C2-C12alkynylsulfonyl, C2-C12 haloalkenylthio, C2-C12haloalkenyisulfinyl, C1-C12haloalkenylsulfonyl, C1-C4alkoxycarbonyl-C1-C4alkylthio, C1-C4alkoxycarbonyl-C1-C4alkylsulfinyl, C1-C4alkoxycarbonyl-C1-C4alkylsulfonyl, (C1-C4alkoxy)2P(O)O, C1-C4alkyl-(C1-C4alkoxy)P(O)O, H(C1-C4alkoxy)P(O)O, R53R54N, R79R80NNH—, R55R56NC(O)O—, R81R82NC(O)NH—, C1-C4alkyl-S(O)2NR57, C1-C4 haloalkyl-S(O)2NR58, C1-C4alkyl-S(O)2O, C1-C4haloalkyl-S(O)2O, C1-C18alkylcarbonyloxy, where the alkyl group may be substituted by halogen, C1-C6alkoxy, C1-C6alkylthio or cyano, C2-C18alkenyicarbonyloxy, C2-C18alkynylcarbonyloxy, C3-C6cycloalkylcarbonyloxy, C1-C12 alkoxycarbonyloxy, C1-C12alkylthiocarbonyloxy, C1-C12alkylthiocarbamoyl, C1-C6alkyl-NH(CS)N(C1-C6alkyl)—NH—, di-C1-C6alkyl-N(CS)N(C1-C6alkyl)—NH—, benzyloxy, benzylthio, benzylsulfinyl, benzylsulfonyl, phenoxy, phenylthio, phenylsulfinyl, phenylsulfonyl, phenylsulfonyloxy or benzoyloxy, where the phenyl groups for their part may each be substituted by C1-C4alkyl, C1-C4haloalkyl, C1-C4alkoxy, C1-C4haloalkoxy, C1-C4alkylcarbonyl, C1-C4alkoxycarbonyl, C1-C4alkylamino, di-C1-C4alkylamino, C1-C4alkylthio, C1-C4alkylsulfinyl, C1-C4alkylsulfonyl, C1-C4alkyl-S(O)2O, C1-C4haloalkylthio, C1-C4haloalkylsulfinyl, C1-C4 haloalkylsulfonyl, C1-C4haloalkyl-S(O)2O, C1-C4alkyl-S(O)2NH, C1-C4alkyl-S(O)2N(C1-C4 alkyl), halogen, nitro or cyano, or a group Ar11-thio, Ar12-sulfinyl, Ar13-sulfonyl, —OCO—Ar14 or NH—Ar15 in which Ar11, Ar12, Ar13, Ar14 and Ar15 independently of one another are a five- to ten-membered monocyclic or fused bicyclic ring system which may be aromatic or partially saturated and may contain 1 to 4 heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur, and in which each ring system may not contain more than 2 oxygen atoms and not more than two sulfur atoms, and in which the ring system for its part may be mono-, di- or trisubstituted by C1-C6alkyl, C1-C6haloalkyl, C3-C6alkenyl, C3-C6haloalkenyl, C3-C6alkynyl, C3-C6haloalkynyl, C1-C6alkoxy, C1-C6haloalkoxy, C3-C6alkenyloxy, C3-C6alkynyloxy, mercapto, C1-C6alkylthio, C1-C6haloalkylthio, C3-C6alkenylthio, C3-C6haloalkenylthio, C3-C6alkynylthio, C2-C5 alkoxyalkylthio, C3-C5acetylalkylthio, C3-C6alkoxycarbonylalkylthio, C2-C4cyanoalkylthio, C1-C6alkylsulfinyl, C1-C6haloalkylsulfinyl, C1-C6alkylsulfonyl, C1-C6haloalkylsu ffonyl, aminosulfonyl, C1-C2alkylaminosulfonyl, C2-C4dialkylaminosulfonyl, C1-C3alkylene-R59, NR60R61, halogen, cyano, nitro, phenyl and benzylthio, where phenyl and benzylthio for their part may be substituted on the phenyl ring by C1-C3alkyl, C1-C3haloalkyl, C1-C3alkoxy, C1-C3haloalkoxy, halogen, cyano or nitro, and where substituents on the nitrogen in the heterocyclic ring are different from halogen; R59 is C1-C3alkoxy, C2-C4alkoxycarbonyl, C1-C3alkylthio, C1-C3alkylsulfinyl, C1-C3alkylsulfonyl or phenyl, where phenyl for its part may be substituted by C1-C3alkyl, C1-C3haloalkyl, C1-C3 alkoxy, C1-C3haloalkoxy, halogen, cyano or nitro; R60 is hydrogen or C1-C6alkyl; R61 is C1-C6alkyl or C1-C6alkoxy; R55, R53, R57, R58, R79 and R81 independently of one another are hydrogen or C1-C4alkyl; R56, R54, R80 and R82 independently of one another are hydrogen, C1-C12alkyl, hydroxyl, C1-C12alkoxy, C3-C6alkenyloxy or C3-C6alkynyloxy; or R53 and R54 together or R55 and R56 together or R79 and R80 together or R81 and R82 together are pyrrolidino, piperidino, morpholino, thiomorpholino, which may be mono- or polysubstituted by methyl groups; R29 is hydrogen, C1-C6alkyl, C1-C4alkylcarbonyl, C1-C4alkoxycarbonyl, (C1-C4alkyl)NHCO, phenylaminocarbonyl, benzylaminocarbonyl or (C1-C4alkyl)2NCO, where the phenyl and benzyl groups for their part may each be substituted by C1-C4alkyl, C1-C4haloalkyl, C1-C4 alkoxy, C1-C4haloalkoxy, C1-C4alkylcarbonyl, C1-C4alkoxycarbonyl, C1-C4alkylamino, di-C1-C4 alkylamino, C1-C4alkylthio, C1-C4alkylsulfinyl, C1-C4alkylsulfonyl, C1-C4alkyl-S(O)2O, C1-C4 haloalkylthio, C1-C4haloalkylsulfinyl, C1-C4haloalkylsulfonyl, C1-C4haloalkyl-S(O)2O, C1-C4 alkyl-S(O)2NH, C1-C4alkyl-S(O)2N(C1-C4alkyl), halogen, nitro or cyano; or is the group Q4 in whichR30 is hydroxyl, O−M+, halogen, cyano, SCN, OCN, C1-C12alkoxy, C1-C4alkoxycarbonyl-C1-C4 alkoxy, C1-C12alkylthio, C1-C12alkylsulfinyl, C1-C12alkyisulfonyl, C1-C12haloalkylthio, C1-C12 haloalkylsulfinyl, C1-C12haloalkylsulfonyl, C1-C6alkoxy-C1-C6alkylthio, C1-C6alkoxy-C1-C6 alkylsu ifinyl, C1-C6alkoxy-C1-C6alkylsulfonyl, C2-C12alkenylthio, C2-C12alkenylsulfinyl, C2-C12 alkenylsulfonyl, C2-C12alkynylthio, C2-C12alkynylsulfinyl, C2-C2alkynylsulfonyl, C2-C12 haloalkenylthio, C2-C12haloalkenylsulfinyl, C2-C12haloalkenylsulfonyl, C1-C4alkoxycarbonyl-C1-C4alkylthio, C1-C4alkoxycarbonyl-C1-C4alkylsulfinyl, C1-C4alkoxycarbonyl-C1-C4alkylsulfonyl, (C1-C4alkoxy)2P(O)O, C1-C4alkyl-(C1-C4alkoxy)P(O)O, H(C1-C4alkoxy)P(O)O, R62R63N, R83R84NNH—, R64R65NC(O)—, R85R86NC(O)NH—, C1-C4alkyl-S(O)2NR66, C1-C4 haloalkyl-S(O)2NR67, C1-C4alkyl-S(O)2O, C1-C4haloalkyl-S(O)2O, C1-C18alkylcarbonyloxy, where the alkyl group may be substituted by halogen, C1-C6alkoxy, C1-C6alkylthio or cyano, C2-C18alkenylcarbonyloxy, C2-C18alkynylcarbonyloxy, C3-C6cycloalkylcarbonyloxy, C1-C12 alkoxycarbonyloxy, C1-C12alkylthiocarbonyloxy, C1-C12alkylthiocarbamoyl, C1-C6alkyl-NH(CS)N(C1-C6alkyl)—NH—, di-C1-C6alkyl-N(CS)N(C1-C6alkyl)—NH—, benzyloxy, benzylthio, benzylsulfinyl, benzylsulfonyl, phenoxy, phenylthio, phenylsulfinyl, phenylsulfonyl, phenylsulfonyloxy or benzoyloxy, where the phenyl groups for their part may each be substituted by C1-C4alkyl, C1-C4haloalkyl, C1-C4alkoxy, C1-C4haloalkoxy, C1-C4alkylcarbonyl, C1-C4alkoxycarbonyl, C1-C4alkylamino, di-C1-C4alkylamino, C1-C4alkylthio, C1-C4alkylsulfinyl, C1-C4alkylsulfonyl, C1-C4alkyl-S(O)2O, C1-C4haloalkylthio, C1-C4haloalkylsulfinyl, C1-C4 haloalkylsulfonyl, C1-C4haloalkyl-S(O)2O, C1-C4alkyl-S(O)2NH, C1-C4alkyl-S(O)2N(C1-C4 alkyl), halogen, nitro or cyano, or a group Ar16-thio, Ar17sulfinyl, Ar18-sulfonyl, —OCO—Ar19 or NH—Ar20 in which Ar16, Ar17, Ar18, Ar19 and Ar20 independently of one another are a five- to ten-me mbered monocyclic or fused bicyclic ring system which may be aromatic or partially saturated and may contain 1 to 4 heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur, and in which each ring system may not contain more than 2 oxygen atoms and not more than two sulfur atoms, and in which the ring system for its part may be mono-, di- or trisubstituted by C1-C6alkyl, C1-C6haloalkyl, C3-C6alkenyl, C3-C6haloalkenyl, C3-C6alkynyl, C3-C6haloalkynyl, C1-C6alkoxy, C1-C6haloalkoxy, C3-C6alkenyloxy, C3-C6alkynyloxy, mercapto, C1-C6alkylthio, C1-C6haloalkylthio, C3-C6alkenylthio, C3-C6haloalkenylthio, C3-C6alkynylthio, C2-C5 alkoxyalkylthio, C3-C5acetylalkylthio, C3-C6alkoxycarbonylalkylthio, C2-C4cyanoalkylthio, C1-C6alkylsulfinyl, C1-C6haloalkylsulfinyl, C1-C6alkylsulfonyl, C ,-C6haioalkyisulfonyl, aminosulfonyl, C1-C2alkylaminosulfonyl, C2-C4dialkylaminosulfonyl, C1-C3alkylene-R68, NR69R70, halogen, cyano, nitro, phenyl and benzylthio, where phenyl and benzylthio for their part may be substituted on the phenyl ring by C1-C3alkyl, C1-C3haloalkyl, C1-C3alkoxy, C1-C3haloalkoxy, halogen, cyano or nitro, and where substituents on the nitrogen in the heterocyclic ring are different from halogen; R68 is C1-C3alkoxy, C2C4alkoxycarbonylt, C1-C3alkylthio, C1-C3alkylsulfinyl, C1-C3alkylsulfonyl or phenyl, where phenyl for its part may be substituted by C1-C3alkyl, C1-C3haloalkyl, C1-C3 alkoxy, C1-C3haloalkoxy, halogen, cyano or nitro; R70 is hydrogen or C1-C6alkyl; R61 is C1-C6alkyl or C1-C6alkoxy; R64, R62, R66, R67, R83 and R85 independently of one another are hydrogen or C1-C4alkyl; R65, R63, R84 and R86 independently of one another are hydrogen, C1-C12alkyl, hydroxyl, C1-C12alkoxy, C3-C6alkenyloxy or C3-C6alkynyloxy; or R62 and R63 together or R64 and R65 together or R83 and R84 together or R85 and R86 together are pyrrolidino, piperidino, morpholino, thiomorpholino, which may be mono- or polysubstituted by methyl groups; R33 and R34 independently of one another are hydrogen, C1-C4alkyl, C2-C6alkenyl, C2-C6 alkynyl, C1-C4alkoxycarbonyl, C1-C6alkylthio, C1-C6alkylsulfinyl, C1-C6alkylsulfonyl, C1-C4 alkyl-NHS(O)2, C1-C4haloalkyl, —NH—C1-C4alkyl, —N(C1-C4alkyl )2, C1-C6alkoxy or phenyl, which for its part may be substituted by C1-C4alkyl, C1-C4haloalkyl, C1-C4alkoxy, C1-C4haloalkoxy, C1-C4alkylcarbonyl, C1-C4alkoxycarbonyl, amino, C1-C4alkylamino, di-C1-C4alkylamino, C1-C6 alkylthio, C1-C6alkylsulfinyl, C1-C6alkylsulfonyl, C1-C4alkyl-S(O)2O, C1-C4haloalkylthio, C1-C4 haloalkylsulfinyl, C1-C4haloalkylsulfonyl, C1-C4haloalkyl-S(O)2O, C1-C4alkyl-S(O)2NH, C1-C4 alkyl-S(O)2N(C1-C4alkyl), halogen, nitro, COOH or cyano; or R33 and R34 together forrn a C2-C6alkylene bridge; and R35 is hydrogen, C1-C6alkyl, C3-C6alkenyl, C3-C6alkynyl or benzyl, which for its part may be substituted by halogen, methyl or methoxy, or is C1-C4alkoxycarbonyl or phenyl, which for its part may be substituted by C1-C4alkyl, C1-C4haloalkyl, C1-C4alkoxy, C1-C4haloalkoxy, C1-C4 alkylcarbonyl, C1-C4alkoxycarbonyl, amino, C1-C4alkylamino, di-C1-C4alkylamino, C1-C4 alkylthio, C1-C4alkylsulfinyl, C1-C4alkylsulfonyl, C1-c4alkyl-S(O)2O, C1-C4haloalkylthio, C1-C4 haloalkylsulfinyl, C1-C4haloalkylsulfonyl, C1-C4haloalkyl-S(O)2O, C1-C4alkyl-S(O)2NH, C1-C4 alkyl-S(O)2N(C1-C4alkyl), halogen, nitro, COOH or cyano; or is the group Q5 in whichZ is S, SO or SO2; R01 is hydrogen, C1-C8alkyl, C1-C8alkyl substituted by halogen, C1-C4alkoxy, C1-C4alkylthio, C1-C4alkylsulfonyl, C1-C4alkylsulfinyl, —CO2R02, —COR03, —COSR04, —NR05R06, CONR036R037 or phenyl, which for its part may be substituted by C1-C4alkyl, C1-C6haloalkyl, C1-C4alkoxy, C1-C4haloalkoxy, C2-C6alkenyl, C3-C6alkynyl, C3-C6alkenyloxy, C3-C6alkynyloxy, halogen, nitro, cyano, —COOH, COOC1-C4alkyl, COOphenyl, C1-C4alkoxy, phenoxy, (C1-C4alkoxy)-C1-C4 alkyl, (C1-C4alkylthio)-C1-C4alkyl, (C1-C4alkylsulfinyl)-C1-C4alkyl, (C1-C4alkylsulfonyl)-C1-C4 aikyl, NHSO2—C1-C4alkyl, NHSO2-phenyl, N(C1-C6alkyl)SO2—C1-C4alkyl, N(C1-C6alkyl)SO2-phenyl, N(C2-C6alkenyl)SO2—C1-C4alkyl, N(C2-C6alkenyl)SO2-phenyl, N(C3-C6alkynyl)SO2—C1-C4alkyl, N(C3-C6alkynyl)SO2-phenyl, N(C3-C7cycloalkyl)SO2—C1-C4alkyl, N(C3-C7 cycloalkyl)SO2-phenyl, N(phenyl)SO2—C1-C4alkyl, N(phenyl)SO2-phenyl, OSO2—C1-C4alkyl, CONR25R26, OSO2—C1-C4haloalkyl, OSO2-phenyl, C1-C4alkylthio, C1-C4haloalkylthio, phenylthio, C1-C4alkylsulfonyl, C1-C4haloalkylsulfonyl, phenylsulfonyl, C1-C4alkylsulfinyl, C1-C4haloalkylsulfinyl, phenylsulfinyl, C1-C4alkylene-phenyl or —NR015CO2R027; or R01 is C2-C8alkenyl or C2-C8alkenyl substituted by halogen, C1-C4alkoxy, C1-C4alkylthio, C1-C4alkylsulfonyl, C1-C4alkylsulfinyl, —CONR032R033, cyano, nitro, —CHO, —CO2R038, —COR039, —COS—C1-C4alkyl, —NR034R035 or phenyl which for its part may be substituted by C1-C4alkyl, C1-C6haloalkyl, C1-C4alkoxy, C1-C4haloalkoxy, C2-C6alkenyl, C3-C6alkynyl, C3-C6alkenyloxy, C3-C6alkynyloxy, halogen, nitro, cyano, —COOH, COOC1-C4alkyl, COOphenyl, C1-C4alkoxy, phenoxy, (C1-C4alkoxy)-C1-C4alkyl, (C1-C4alky fthio)-C1-C4alkyl, (C1-C4alkylsulfinyl)-C1-C4alkyl, (C1-C4alkylsulfonyl)-C1-C4alkyl, NHSO2—C1-C4alkyl, NHSO2-phenyl, N(C1-C6alkyl)SO2—C1-C4 alkyl, N(C1-C6alkyl)SO2-phenyl, N(C2-C6alkenyl)SO2—C1-C4alkyl, N(C2-C ralkenyl)SO2-phenyl, N(C3-C6alkynyl)SO2—C1-C4alkyl, N(C3-C6alkynyl)SO2-phenyl, N(C3-C7cycloalkyl)SO2—C1-C4 alkyl, N(C3-C7cycloalkyl)SO2-phenyl, N(phenyl)SO2—C1-C4alkyl, N(phenyl)SO2-phenyl, OSO2-C1-C4alkyl, CONR040R041, OSO2—C1-C4haloalkyl, OSO2-phenyl, C1-C4alkylthio, C1-C4 haioalkylthio, phenylthio, C1-C4alkylsulfonyl, C1-C4haloalkylsulfonyl, phenylsulfonyl, C1-C4 alkylsulfinyl, C1-C4haloalkylsulfinyl, phenylsulfinyl, C1-C4alkylene-phenyl or —NR043CO2R042; or R01 is C3-C6alkynyl or C3-C6alkynyl substituted by halogen, C1-C4haloalkyl, cyano, —CO2R044 or phenyl, which for its part may be substituted by C1-C4alkyl, C1-C6haloalkyl, Cl-C4 alkoxy, C1-C4haloalkoxy, C2-C6alkenyl, C3-C6alkynyl, C3-C6alkenyloxy, C3-C6alkynyloxy, halogen, nitro, cyano, —COOH, COOC1-C4alkyl, COOphenyl, C1-C4alkoxy, phenoxy, (C1-C4 alkoxy)-C1-C4alkyl, (C1-C4alkylthio)-C1-C4alkyl, (C1-C4alkylsulfinyl)-C1-C4alkyl, (C1-C4 alkylsulfonyl)-C1-C4alkyl, NHSO2—C1-C4alkyl, NHSO2-phenyl, N(C1-C6alkyl)SO2—C1-C4alkyl, N(C1-C6alkyl)SO2-phenyl, N(C2-C6alkenyl)SO2—C1-C4alkyl, N(C2-C6alkenyl)SO2-phenyl, N(C3-C6alkynyl)SO2—C1-C4alkyl, N(C3-C6alkynyl)SO2-phenyl, N(C3-C7cycloalkyl)SO2—C1-C4alkyl, N(C3-C7cycloalkyl)SO2-phenyl, N(phenyl)SO2—C1-C4alkyl, N(phenyl)SO2-phenyl, OS2O-C1-C4 alkyl, CONR028R029, OSO2—C1-C4haloalkyl, OSO2-phenyl, C1-C4alkylthio, C1-C4haloalkylthio, phenylthio, C1-C4alkylsulfonyl, C1-C4haloalkylsulfonyl, phenylsulfonyl, C1-C4alkylsulfinyl, C1-C4haloalkylsulfinyl, phenylsulfinyl, C1-C4alkylene-phenyl or —NR031CO2R030; or R01 is C3-C7cycloalkyl, C3-C1cycloalkyl substituted by C1-C4alkyl, C1-C4alkoxy, C1-C4 alkylthio, C1-C4alkylsulfinyl, C1-C4alkylsulfonyl or phenyl, which for its part may be substituted by halogen, nitro, cyano, C1-C4alkoxy, C1-C4haloalkoxy, C1-C4alkylthio, C1-C4haloalkylthio, C1-C4alkyl and C1-C4haloalkyl; or R01 is C1-C4alkylene-C3-C7cycloalkyl, phenyl, or phenyl which is substituted by C1-C4alkyl, C1-C6haloalkyl, C1-C4alkoxy, C1-C4haloalkoxy, C2-C6alkenyl, C3-C6alkynyl, C3-C6alkenyloxy, C3-C6alkynyloxy, halogen, nitro, cyano, —COOH, COOC1-C4alkyl, COOphenyl, C1-C4alkoxy, phenoxy, (C1-C4alkoxy)-C1-C4alkyl, (C1-C4alkylthio)-C1-C4alkyl, (C1-C4alkylsulfinyl)-C1-C4alkyl, (C1-C4alkylsul fonyl)-C1-C4alkyl, NHSO2—C1-C4alkyl, NHSO2-phenyl, N(C1-C6alkyl)SO2-C1-C4 alkyl, N(C1-C6alkyl)SO2-phenyl, N(C2-C6alkenyl)SO2—C1-C4alkyl, N(C2-C6alkenyl)SO2-phenyl, N(C3-C6alkynyl)SO2—C1-C4alkyl, N(C3-C6alkynyl)SO2-phenyl, N(C3-C7cycloalkyl)SO2—C1-C4 alkyl, N(C3-C7cycloalkyl)SO2-phenyl, N(phenyl)SO2—C1-C4alkyl, N(phenyl)SO2-phenyl, OSO2—C1-C4alkyl, CONR045R046, OSO2—C1-C4haloalkyl, OSO2-phenyl, C1-C4alkylthio, C1-C4 haloalkylthio, phenylthio, C1-C4alkylsulfonyl, C1-C4haloalkylsulfonyl, phenylsulfonyl, C1-C4 alkylsulfinyl, C1-C4haloalkylsulfinyl, phenylsulfinyl, or —NR048CO2R047; or R01 is C1-C4alkylene-phenyl, COR07 or 4-6-membered heterocyclyl; R02, R038, R044 and R066 independently of one another are hydrogen, C1-C4alkyl, phenyl, or phenyl which is substituted by C1-C4alkyl, C1-C6haloalkyl, C1-C4alkoxy, C1-C4haloalkoxy, C2-C6alkenyl, C3-C6alkynyl, C3-C6alkenyloxy, C3-C6alkynyloxy, halogen, nitro, cyano, —COOH, COOC1-C4alkyl, Coophenyl, C1-C4alkoxy, phenoxy, (C1-C4alkoxy)-C1-C4alkyl, (C1-C4 alkylthio)-C1-C4alkyl, (C1-C4alkylsulfinyl)-C1-C4alkyl, (C1-C4alkylsulfonyi)-C1-C4alkyl, NHSO2—C1-C4alkyl, NHSO2-phenyl, N(C1-C6alkyl)SO2—C1-C4alkyl, N(C1-C6alkyl)SO2-phenyl, N(C2-C6 alkenyl)SO2—C1-C4alkyl, N(C2-C6alkenyl)SO2-phenyl, N(C3-C6alkynyl)SO2—C1-C4alkyl, N(C3-C6 alkynyl)SO2-phenyl, N(C3-C7cycloalkyl)SO2—C1-C4alkyl, N(C3-C7Cyloalkyl)SO2-phenyl, N(phenyl)SO2—C1-C4alkyl, N(phenyl)SO2-phenyl, OSO2-C1-C4alkyl, CONR049R050, OSO2—C1-C4 haloalkyl, OSO2-phenyl, C1-C4alkylthio, C1-C4haloalkylthio, phenylthio, C1-C4alkylsulfonyl, C1-C4haloalkylsulfonyl, phenylsulfonyl, C1-C4alkylsulfinyl, C1-C4haloalkylsulfinyl, phenylsulfinyl, C1-C4alkylene-phenyl or —NR052CO2R053; R03, R039 and R067 independently of one another are C1-C4alkyl, phenyl or phenyl which is substituted by C1-C4alkyl, C1-C6haloalkyl, C1-C4alkoxy, C1-C4haloalkoxy, C2-C6alkenyl, C3-C6 alkynyl, C3-C6alkenyloxy, C3-C6alkynyloxy, halogen, nitro, cyano, —COOH, COOC1-C4alkyl, COOphenyl, C1-C4alkoxy, phenoxy, (C1-C4alkoxy)-C1-C4alkyl, (C1-C4alkylthio)-C1-C4alkyl, (C1-C4alkylsulfinyl)-C1-C4alkyl, (C1-C4alkylsulfonyl)-C1-C4alkyl, NHSO2—C1-C4alkyl, NHSO2-phenyl, N(C1-C6alkyl)SO2—C1-C4alkyl, N(C1-C6alkyl)SO2-phenyl, N(C2-C6alkenyl)SO2—C1-C4alkyl, N(C2-C6alkenyl)S)2-phenyl, N(C3-C6alkynyl)SO2—C1-C4alkyl, N(C3-C6alkynyl)SO2-phenyl, N(C3-C7 cycloalkyl)SO2—C1-C4alkyl, N(C3-7cycloalkyl)SO2-phenyl, N(phenyl)SO2-C1-C4alkyl, N(phenyl)SO2-phenyl, OSO2-C1-C4alkyl, CONR070R054, OSO2—C1-C4haloalkyl, OSO2-phenyl, C1-C4alkylthio, C1-C4haloalkylthio, phenylthio, C1-C4alkylsulfonyl, C1-C4haloalkylsulfonyl, phenylsulfonyl, C1-C4alkylsulfinyl, C1-C4haloalkylsulfinyl, phenylsulfinyl, C1-C4alkylene-phenyl or —NR056CO2R055; R04 is C1-C4alkyl; R05 is hydrogen, C1-C4alkyl, C2-C6alkenyl, C3-C6alkynyl, C3-C7cycloalkyl, phenyl or phenyl which is substituted by C1-C4alkyl, C1-C6haloalkyl, C1-C4alkoxy, C1-C4haloalkoxy, C2-C6 alkenyl, C3-C6alkynyl, C3-C6alkenyloxy, C3-C6alkynyloxy, halogen, nitro, cyano, —COOH, COOC1-C4alkyl, COOphenyl, C1-C4alkoxy, phenoxy, (C1-C4alkoxy)-C1-C4alkyl, (C1-C4 alkylthio)-C1-C4alkyl, (C1-C4alkylsulfinyl)-C1-C4alkyl, (C1-C4alkylsulfonyl)-C1-C4alkyl, NHSO2—C1-C4alkyl, NHSO2-phenyl, N(C1-C6alkyl)SO2—C1-C4alkyl, N(C1-C6alkyl)SO2-phenyl, N(C2-C6 alkenyl)SO2—C1-C4alkyl, N(C2-C6alkenyl)SO2-phenyl, N(C3-C6alkynyl)SO2H, N(C3-C6 alkynyl)SO2—C1-C4alkyl, N(C3-C6alkynyl)SO2phenyl, N(C3-C7cycloalkyl)SO2H, N(C3-C7 cycloalkyl)SO2—C1-C4alkyl, N(C3-C7cycloalkyl)SO2-phenyl, N(phenyl)SO2—C1-C4alkyl, N(phenyl)SO2-phenyl, OSO2-C1-C4alkyl, CONR057R058, OSO2—C1-C4haloalkyl, OSO2-phenyl, C1-C4alkylthio, C1-C4ha hoalkylthio, phenylthio, C1-C4alkylsulfonyl, C1-C4haloalkylsulfonyl, phenylsulfonyl, C1-C4alkylsulfinyl, C1-C4haloalkylsulfinyl, phenylsulfinyl, C1-C4alkylenephenyl or —NR060CO2R059; R06 is hydrogen, C1-C4alkyl, C2-C6aikenyl, C3-C6alkynyl, C3-C7cycloalkyl, phenyl or phenyl which is substituted by C1-C4alkyl, C1-C6haloalkyl, C1-C4alkoxy, C1-C4haloalkoxy, C2-C6 alkenyl, C3-C6alkynyl, C3-C6alkenyloxy, C3-C6alkyny loxy, halogen, nitro, cyano, —COOH, COOC1-C4alkyl, COOphenyl, C1-C4alkoxy, phenoxy, (C1-C4alkoxy)-C1-C4alkyl, (C1-C4 alkylthio)-C1-C4alkyl, (C1-C4alkylsulfinyl)C1-C4alkyl, (C1-C4alkylsulfonyl)-C1-C4alkyl, NHSO2—C1-C4alkyl, NHSO2-phenyl, N(C1-C6alkyl)SO2—C1-C4alky l, N(C1-C6alkyl)SO2-phenyl, N(C2-C6 alkenyl)SO2—C1-C4alkyl, N(C2-C6alkenyl)SO2-phenyl, N(C3-C6alkynyl)SO2—C1-C4alkyl, N(C3-C6 alkynyl)SO2-phenyl, N(C3-C7cycloalkyl)SO2—C1-C4alkyl, N(C3-C7cycloalkyl)SO2-phenyl, N(phenyl)SO2—C1-C4alkyl, N(phenyl)SO2-phenyl, OS02-C1-C4alkyl, CONR061R062, OSO2—C1-C4 haloalkyl, OSO2-phenyl, C1-C4alkylthio, C1-C4haloalkylthio, phenylthio, C1-C4alkylsulfonyl, C1-C4haloalkylsulfonyl, phenylsulfonyl, C1-C4alkylsulfinyl, C1-C4haloalkylsulfinyl, phenylsulfinyl, C1-C4alkylene-phenyl or —NR064CO2R063; R07 is phenyl, substituted phenyl, C1-C4alkyl, C1-C4alkoxy or —NR08R09; R08 and R09 independently of one another are C1-C4alkyl, phenyl or phenyl which is substituted by halogen, nitro, cyano, C1-C4alkyl, C1-C4alkoxy, C1-C4thioalkyl, —CO2R066, —COR067, C1-C4alkylsulfonyl, C1-C4alkylsulfinyl, C1-C4haloalkyl; or R08 and R09 together form a 5-6-membered ring which may be interrupted by oxygen, NR065 or S, R015, R031, R043, R048, R052, R056, R060 and R064 independently of one another are hydrogen, C1-C4alkyl, C2-C6alkenyl, C3-C6alkynyl or C3-C7cycloalkyl; R025, R026, R027, R028, R029, R030, R032, R033, R034, R035, R036, R037, R040, R041, R042, R045, R046, R047, R049, R050, R053, R054, R055, R057, R058, R059, R061, R062, R063, R065 and R070 independently of one another are hydrogen, C1-C4alkyl, C2-C6alkenyl, C3-C6alkynyl, C3-C7cycloalkyl, phenyl, or phenyl which is substituted by halogen, nitro, cyano, C1-C4alkoxy, C1-C4haloalkoxy, C1-C4 alkylthio, C1-C4haloalkylthio, C1-C4alkyl or C1-C4haloalkyl; and R36 is C1-C4alkyl, C1-C4haloalkyl, C3-C6alkenyl, C3C6haloalkenyl, C3-C6alkynyl, C3-C6 haloalkynyl, C3-C6cycloalkyl or C3-C6cycloalkyl which is substituted by halogen, C1-C4alkyl, C1-C4haloalkyl, C3-C6alkenyl, C3-C6haloalkenyl, C3-C6aIkynyl, C3-C6haloalkynyt, C1-C4 alkoxycarbonyl, C1-C4alkylthio, C1-C4alkylsulfinyl, C1-C4alkylsulfonyl, C1-C4haloalkylthio, C1-C4haloalkylsulfinyl, C1-C4haloalkylsulfonyl, C1-C4alkylcarbonyl, di-C1-C4alkylamino, C1-C4 alkoxy, C1-C4haloalkoxy, C1-C4alkyl-S(O)2O, C1-C4haloalkyl-S(O)2O or phenyl which for its part may be substituted by halogen, C1-C4alkyl, C1-C4haloalkyl, C3-C6alkenyl, C3-C6alkynyl, cyano, nitro or COOH; and agronomically acceptable salts M+ and all stereoisomers and tautomers of the compounds of the formula I.
2. A herbicidal and plant-growth-inhibiting composition, which contains a herbicidally effective amount of a compound of the formula I, according to claim 1, on an inert carrier.
3. A method for controlling undesirable plant growth, wherein a herbicidally effective amount of an active compound of the formula I, according to claim 1, or a composition which contains this active compound is applied to the plants or their habitat.
4. A method for inhibiting plant growth, wherein a herbicidally effective amount of an active compound of the formula I, according to claim 1, or a composition which contains this active compound is applied to the plants or their habitat.

Priority Claims (1)

Number	Date	Country	Kind
1873/98	Sep 1998	CH

Parent Case Info

This application is a Continuation of PCT/EP99/06761 filed Sep. 13, 1999.

US Referenced Citations (1)

Number	Name	Date	Kind
4747871	Ruminski et al.	May 1988	A

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Continuations (1)

	Number	Date	Country
Parent	PCT/EP99/06761	Sep 1999	US
Child	09/804507		US

Pyridine ketones useful as herbicides

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Abstract