AU744632B2 - Fungicidal methods, compounds and compositions containing benzophenones - Google Patents

Description

I

II

I S F Ref: 326280D1

AUSTRALIA

PATENTS ACT 1990 COMPLETE SPECIFCATION FOR A STANDARD PATENT

ORIGINAL

Name and Address of Applicant: Actual Inventor(s): Address for Service: Invention Title: American Cyanamid Company Five Giralda Farms Madison New Jersey 07940 0874 UNITED STATES OF AMERICA Juergen Curtze, Christine Helene Gertrud Rudolph, Ludwig Schroeder, Guido Albert, Annerose Edith Elise Rehnig and Ewald Gerhard Sieverding Spruson Ferguson, Patent Attorneys Level 33 St Martins Tower, 31 Market Street Sydney, New South Wales, 2000, Australia Fungicidal Methods, Compounds and Compositions Containing Benzophenones The following statement is a full description of this invention, including the best method of performing it known to me/us:- 5845

'A

FUNGICIDAL METHODS. COMPOUNDS AND COMPOSITIONS CONTAINING BENZOPHENONES BACKGROUND OF THE INVENTION Food production relies upon a variety of agricultural technologies to ensure the growing population's dietary needs remain affordable, nutritious and readily available on grocery store shelves. Fungicides are one of these 5 agricultural technologies which are available to the world community. Fungicides are agrochemical compounds which shield crops and foods from fungus and fungal diseases.

Crops and food are constantly threatened by a variety of fungal organisms, which, if left uncontrolled, can cause 10 ruined crops and devastated harvests.

In particular, ascomycetes, the causative agent for powdery mildew diseases are an ever-present threat especially to cereal and fruit crops. However, applications of fungicidal agents at disease control rates can cause 15 phytotoxic damage to the target plants.

Therefore it is an object of this invention to provide a method to control phytopathogenic fungus without causing concurrent phytotoxic damage to the host plant.

It is another object of this invention to provide an effective and safe method for the protection of important agronomic crops from the damage and loss caused by a phytopathogenic fungal infection and the disease caused thereby.

NIW41RJl~ 2 It is a further object of this invention to provide benzophenone fungicidal agents and fungicidal compositions comprising a benzophenone compound.

These and other objects and features of the invention Swill become apparent from the detailed description provided Shereinbelow.

SUMMARY OF THE INVENTION The present invention provides a method for the control of a phytopathogenic fungus or a disease caused thereby which comprises contacting said fungus with a fungicidally effective amount of a benzophenone compound of formula I R R X R 3 (R (R 4 "y r Y

R

(I)

wherein R 1 represents a halogen atom, an optionally substituted alkyl or alkoxy group, a cyano or a nitro group; m is 0 or an integer of 1, 2, 3 or 4; R 2 independently represents a halogen atom, an optionally substituted alkyl or alkoxy group, a nitro group or when R' and R' are attached to 25 adjacent carbon atoms, R 1 and one R 2 may be taken together to represent -CH=CH-CH=CH- or optionally substituted alkylene or oxyalkyleneoxy, such as O-CF,-O; R 3 represents hydrogen, halogen, an optionally substituted alkyl, alkoxy, alkenyl, alkylthio, alkylsulphinyl, alkylsulphonyl, cyano, carboxy, hydroxy, nitro, or an optionally substituted amino group; R 4 3 represents a hydrogen atom or an optionally substituted alkyl or acyl group; R 5 represents a hydrogen, halogen, an optionally substituted alkyl, alkoxy, alkenyloxy, alkynyloxy, alkylthio, cycloalkyl, cycloalkyloxy, a nitro, hydroxy, phenoxy, trialkylsilyloxy group, -ONa, -OK, -OC(O)R 7

-OCHR

8

C(O)R

7

-OC(O)NR

8

R

9

-OS(O)

2

R

8 -OS(0) 2

NR

8

R

9

-OP(X')(OR')OR

9

-OP(X')(R

8

)R

9

-S(O)R

8 or -S(0) 2

R

8 or

R

4 and R 5 may be taken together to represent an optionally substituted alkylene or alkyleneoxy chain; n is 0, or an integer of 1 or 2; R 6 independently represents a halogen atom, an optionally substituted alkyl, alkenyl, alkynyl, alkoxy, alkenyloxy, alkynyloxy, cycloalkyl, cycloalkoxy, hydroxy, -OC(O)R' 0 group, or when R 5 and R 6 are attached to adjacent carbon atoms, R 5 and one R 6 may be taken together to represent -CH=CH-CH=CH- or an optionally substituted oxyalkyleneoxy chain; R 7 represents a hydrogen atom or an optionally substituted alkyl, alkoxy or aryl group; R 8

R

9 and R 1 o independently represent a hydrogen atom, an alkyl, aryl or aralkyl group, or R 8 and R 9 may be taken together to represent an alkylene chain optionally interrupted by an oxygen or nitrogen atom; X represents an oxygen atom, a sulphur atom or a group NOR; X' represents an oxygen or sulphur atom; Y represents an oxygen or sulphur atom or a sulphonyl or sulphinyl group; and R represents a hydrogen atom or an optionally 15 substituted alkyl, aralkyl, aryl or acyl group.

As used in the specification and claims, the term "benzophenone" encompasses oxime derivatives of benzophenone (X=NOR), benzothiophenones and the underivatized benzophenone ketone The present invention also provides crop protection methods, fungicidal benzophenone compounds of formula Ia, methods of preparation of said benzophenone compounds and fungicidal compositions comprising at least one formula I or Ia compound and an agriculturally acceptable carrier.

Thus, in a first embodiment, the present invention provides compounds of formula Ia oo R X R 3 6 2 )n

(R

R

wherein R' represents a halogen atom, an optionally substituted alkyl group or a cyano group; m is an integer of 1, 2, 3 or 4; R 2 independently represents a halogen atom, an optionally substituted alkyl or alkoxy group or when R' and R 2 are attached to adjacent carbon atoms, R' and R 2 may be taken together to represent an optionally substituted P 30 tCH=CH-CH=CH or alkylene or oxyalkyleneoxy group; R3 represents a hydrogen or i [R:\LIBZ]05502.doc:[am halogen atom, an optionally substituted alkyl, alkoxy, alkenyl, alkylthio, alkylsulfinyl, alkylsulfonyl, cyano, carboxy, hydroxy, nitro, or an optionally substituted amino group;

R

4 represents an optionally substituted alkyl or acyl group; R 5 represents a halogen atom, an optionally substituted alkoxy, alkenyloxy, alkynyloxy, alkylthio, cycloalkyl, cycloalkyloxy group, trialkylsilyloxy group, ONa, OK, OC(O)R 7

OCHR

8

C(O)R

7

OC(O)NRR

9 S(0) 2

R

8

OS(O)

2

NRR

9

OP(X')(OR')

O

R

9

OP(X')(R)R

9

S(O)R

8 or

S(O)

2

R

8 group or R 4 and R 5 may be taken together to represent an optionally substituted alkylene or alkyleneoxy chain; n is 0, or an integer of 1 or 2; R 6 independently represents an optionally substituted alkoxy group, a hydroxy or an OC(O)R 1 0 group or when R 5 and

R

6 are attached to adjacent carbon atoms, R R 6 may be taken together to represent CH=CH-CH=CH or an optionally substituted oxyalkyleneoxy chain; R 7 represents a hydrogen atom or an optionally substituted alkyl or alkoxy group; R 8

R

9 and R 1 independently represent a hydrogen atom or an alkyl group or R 8 and R 9 may be taken together to represent an alkylene chain optionally interrupted by an oxygen or nitrogen 1: atom; X represents an oxygen atom, a sulfur atom or an NOR group; X' represents an oxygen atom or a sulfur atom; Y represents an oxygen atom, a sulfur atom, a sulfonyl or a i sulfinyl group; and R represents a hydrogen atom or an optionally substituted alkyl, aralkyl, aryl or acyl group; with the provisos that when X is O or S and: when R' represents a halogen atom, then R 2 must be other than a halogen atom or no more than one alkyl or alkoxy group, (ii) when R' represents an alkyl group, then R 2 must be other than alkyl; (iii) when m is 1, then R 2 must be other than an alkoxy group; (iv) when R 3 represents a substituted alkenyl group, then R 3 must be substituted with other than an alkoxy or acyl group; when R 3 represents a haloalkyl group, then R' and R 2 must be other than a haloalkyl group; and (vi) when Y represents an oxygen atom, then R 3 and R 25 must both be other than a hydrogen atom and n must be an integer of 1 or 2.

o In a second embodiment, the invention provides a compound of formula Cl O CH3 Cl R O-CH 3

O

R'

wherein Q represents a hydrogen or a chlorine atom; R represents a hydrogen atom, a C 3 Cs-cycloalkoxy group or a Ci-Cs-alkoxy group optionally substituted with one or more fluorine atoms or one phenyl, phenoxy, phenylthio or benzyloxy group, wherein the [RA\IBZ]05502dc:am phenyl moiety may be substituted by halogen, CI-C 4 -alkyl, Ci-C 4 -alkoxy, trifluoromethyl and/or trifluoromethoxy; and R' represents hydrogen or Ci-Clo-alkyl optionally substituted with one or more halogen, CI-C 4 -alkoxy, phenyl, phenoxy or phenylthio groups, wherein the phenyl moiety may be substituted by halogen, CI-C 4 -alkyl, Ci-C 4 alkoxy, trifluoromethyl or trifluoromethoxy, with the proviso, that when Q and R represent hydrogen, then R' must be other than methyl.

In a third embodiment, the invention provides a compound of formula CH3 O

CH

3

Q

QO-CH

3 CH3 R Q' O

R'

wherein Q and Q' independently represent a hydrogen atom or methyl group; R represents io a hydrogen atom, a C3-Cs-cycloalkoxy group or a Ci-Cs-alkoxy group optionally .substituted by one or more fluorine atoms, a phenyl, phenoxy, phenylthio or benzyloxy group, wherein the phenyl moiety may be substituted with one or more halogen, C 1

-C

4 alkyl, Ci-C 4 -alkoxy, trifluoromethyl or trifluoromethoxy groups; and R' represents hydrogen or Ci-Clo-alkyl optionally substituted with one or more halogen, Ci-C 4 -alkoxy, S s5 phenyl, phenoxy or phenylthio groups, wherein the phenyl moiety may be substituted with one or more halogen, Ci-C 4 -alkyl, Ci-C 4 -alkoxy, trifluoromethyl or trifluoromethoxy groups.

SIn a fourth embodiment, the invention provides a process for the preparation of a compound of formula I R O R 3 6 m R m 4 wherein R' represents a halogen atom, an optionally substituted alkyl or alkoxy group, a cyano or a nitro group; m is 0 or an integer of 1, 2, 3 or 4; R 2 independently represents a halogen atom, an optionally substituted alkyl or alkoxy group, a nitro group or when R' and R 2 are on-adjacent carbon atoms, R' and R 2 may be taken together to represent an optionally substituted CH=CH-CH=CH, alkylene or oxyalkyleneoxy group; R 3 represents a hydrogen or halogen atom, a cyano, carboxy, hydroxy or nitro group or an optionally (R:\LIBZ]05502.doc:lam substituted alkyl, alkoxy, alkenyl, alkylthio, alkylsulfinyl, alkylsulfonyl or amino group;

R

4 represents a hydrogen atom or an optionally substituted alkyl or acyl group; R represents a hydrogen or a halogen atom or a nitro group, an optionally substituted alkyl, alkoxy, alkenyloxy, alkynyloxy, alkylthio, cycloalkyl, cycloalkyloxy, hydroxy, aryloxy, trialkylsilyloxy, ONa, OK, OC(O)R 7

OCHR

8

C(O)R

7

OC(O)NRR

9

S(O)

2

R

8

OS(O)

2

NR'R

9

OP(X)(OR

8 )OR, OP(X1)(R)R 9

S(O)R

8 or S(O) 2

R

8 group or R 4 and R may be taken together to represent an optionally substituted alkylene or alkyleneoxy chain; n is 0 or an integer of 1 or 2; R 6 independently represents a halogen atom, an optionally substituted alkyl, alkenyl, alkynyl, alkoxy, alkenyloxy, alkynyloxy, cycloalkyl, cycloalkoxy, hydroxy or OC(O)R'° group or when R 5 and R 6 are on adjacent carbon atoms, R R 6 may be taken together to represent an optionally substituted CH=CH-CH=CH or oxyalkyleneoxy chain; R 7 represents a hydrogen atom or an optionally substituted alkyl or alkoxy group; R 8

R

9 and R 1 0 independently represent a hydrogen atom or an optionally substituted alkyl, aryl or aralkyl group, or, R 8 and R 9 may S i 15 be taken together to represent an alkylene chain which may be interrupted by an oxygen or nitrogen atom; X represents an oxygen atom or a sulfur atom; and Y represents an oxygen atom, a sulfur atom, a sulfonyl or a sulfinyl group, which comprises reacting a compound of formula II 1

R

2 Z 20 with a compound of formula m 3

R

2 6 z (R) S 4I R z.i

R

(m) wherein R 2

R

3

R

4

R

5

R

6 Y, m and n are as defined for formula I and one ofZ' and

Z

2 represents a hydrogen atom and the other represents the group COCl or one represents a magnesium halide group MgHal, wherein Hal represents a bromine or iodine atom, and the other represents COC1.

RAL In a fifth embodiment, the invention provides a process for the preparation of a N mpound of formula Ib [RALBUHZ]OSS2.doc:Ian 3d

OH

1 3 R N R 6 2(R (R

O

CH3 (Ib) wherein m is 0 or an integer of 1, 2 or 3; R 1 represents a halogen atom, an optionally substituted alkyl or alkoxy group, a cyano or a nitro group; R 2 independently represents a halogen atom, an optionally substituted alkyl or alkoxy group, a nitro group or when R' and R 2 are on adjacent carbon atoms, R 1 and R 2 may be taken together to represent an optionally substituted CH=CH-CH=CH, alkylene or oxyalkyleneoxy group; R 3 represents a hydrogen or halogen atom, a cyano, carboxy, hydroxy or nitro group or an optionally substituted alkyl, alkoxy, alkenyl, alkylthio, alkylsulfinyl, alkylsulfonyl or amino group; n S 10 is 0 or an integer of 1 or 2; R 6 independently represents a halogen atom, an optionally substituted alkyl, alkenyl, alkynyl, alkoxy, alkenyloxy, alkynyloxy, cycloalkyl, cycloalkoxy, hydroxy or OC(O)R'O group; and R 1 0 represents a hydrogen atom or an optionally substituted alkyl, aryl or aralkyl group which comprises reacting a compound of formula VI 1 with at least one molar equivalent of a compound of formula VII 3 2

SR

OCH

3 V (vnD in the presence of at least one molar equivalent of aluminium chloride and a nonpolar solvent to form an intermediate and hydrolysing said intermediate in the presence of an _acid and water to yield the product formula Ib compound.

[R:\LIBZ]05502.doc:lam The invention also provides fungicidal compositions which comprise an agriculturally acceptable carrier and a fungicidally acceptable amount of a compound of the first, second or third embodiments.

The invention also provides a method for the control of a phytopathogenic fungus or a disease caused thereby, which comprises contacting said fungus with a fungicidally effective amount of a compound of the first, second or third embodiments.

9.

9 999* *99999 i y^ [R:\LIBZ]05502.doc:Ian DETAILED DESCRIPTION OF THE INVENTION Huge economic losses have resulted from the devastation and damage of important agronomic and horticultural crops caused by fungal infection and infestation. Pest management strategies, field resistance, and virulent strains have all contributed to agriculturalists' concerns for combatting phytopathogenic fungal disease. In particular, ascomycetes, the causative agents for powdery mildew diseases continues to 0 be a serious concern in cereal crop and fruit production.

Further, in a variety of fungicidal agent applications concomitant phytotoxic injury to the host plant may be observed.

It has now been found that benzophenone compounds of formula I are highly effective fungicidal agents and are particularly effective for controlling mildew diseases such as powdery mildew. Compounds of formula I useful in fungus control methods are those benzophenones having the structure 320 R X R 3 6 S (R 6

SR(R

2

Y

25

RS

(I)

wherein X, Y, R 2 R, m and n are described hereinabove.

Alkyl as a substituent or as a part of other substituents, such as alkoxy or alkylthio may be straightchain or branched and may contain up to eighteen, preferably up to 14, and especially up to 10, carbon atoms, individual examples including: methyl, ethyl, propyl, butyl, pentyl, hexyl, etc. as well as their isomers such as isopropyl, isobutyl, tertiary-butyl, isopentyl, and the like. Lower alkyl or alkoxy groups have from 1 to 10 carbon atoms.

A

cycloalkyl moiety as a substituent or as a part of other substituents suitably contains from 3 to 10, preferably from 3 to 6, carbon atoms. An alkenyl or alkynyl group suitably has from 2 to 6, preferably from 2 to 4 chain members, for example, ethenyl, propenyl, allyl, butenyl and the like as S well as for chains with more than one double bond such as pentadienyl and the like. An alkylene chain usefully has 1 to 5, preferably 1 to 4, members.

An acyl group is formally formed by the removal of *hydroxyl from a carboxyl group, and is used herein to include 15 formyl and optionally substituted alkylcarbonyl and arylcarbonyl groups.

A halogen atom represents fluorine, chlorine, bromine and iodine, preferably chlorine. Preferred haloalkyl moieties are difluoromethyl and trifluoromethyl.

.20 Optionally substituted moieties may be unsubstituted or 0 have from one up to the maximal chemically possible number of substituents. Optional substituents may be any of those customarily employed in the development of biocidal compounds, and/or the modification of such compounds to 25 influence their activity, persistence, penetration and any other property. Specific examples of such substituents include halogen, especially fluorine, chlorine or bromine, nitro, cyano, hydroxy, carboxy, amino, alkyl- or aralkylamino, dialkylamino, cycloalkylamino, piperidyl, piperidinyl, morpholinyl, carbamoyl, aryl- or benzylcarbamoyl, mono- or dialkylcarbamoyl, morpholinocarbonyl, trialkylsilyl, alkyl, alkenyl, alkynyl, alkoxy, alkoxyalkyl, alkoxyalkoxy, cycloalkyl, cycloalkoxy, acyl, optionally substituted benzoyl, benzoxazolyl, 6 alkoxycarbonyl, optionally substituted pyridyl, phenoxy or naphthyl, phenyl or phenyl substituted by one or more substituents selected from the group comprising halogen, alkyl, alkoxy, alkoxyalkyl, alkoxyalkoxy, alkylthio.

phenylthio, benzylthio, aralkoxy, hydroxy, carboxy, carbalkoxy, cyano, optionally substituted amino, nitro, trifluoromethyl, trifluoromethoxy and the like. Alkyl moieties of such optional substituents may have from 1 to 6 carbon atoms, preferably 1 or 2 carbon atoms. If a substituted group mentioned herein does contain two or more substituents, such substituents may be identical or different.

The benzophenone compounds according to formula I are oils, gums, or, predominantly, crystalline solid materials 15 and possess valuable fungicidal properties. For example, they can be used in agriculture, or related fields such as horticulture and viticulture, for the control of phytopathogenic fungi, especially ascomycetes, and powdery mildew disease such as Erysiphe graminis, Podosphaera 2 leucocricha, Uncinula necator and the like. Said benzophenone compounds possess a high fungicidal activity within a wide concentration range and may be used in agriculture without harmful phytotoxic effects.

Preferred formula I compounds useful in the method of 25 invention are those in which R 1 represents a halogen atom or an optionally substituted alkyl or alkoxy group; m is 0 or an integer of 1, 2 or 3; and R 2 independently represents a halogen atom or an optionally substituted alkyl or alkoxy group; or R 1 and R 2 together represent -CH=CH-CH=CH-, oxyalkyleneoxy, difluorooxymethyleneoxy or alkylene; R 3 represents a halogen atom, an optionally substituted alkyl, alkenyl, alkylthio or alkylsulphonyl group, a nitro group, or an optionally substituted amino group; R 5 represents a hydrogen atom, an optionally substituted alkyl, alkoxy, 7 alkenyloxy, alkynyloxy, cycloalkoxy or alkylthio group, a hydroxy group, a trialkylsilyloxy group, or a -OC(O)R 7

-OCHR

8

C(O)R

7

-OC(O)NR

8

R

9 NH-CO-R', -OS(0)2R 8 or OS(O)2NR 8

R

9 group; or R 4 and R 5 together represent an S optionally substituted alkyleneoxy chain; n is 0 or-the integer 1; R 6 represents an optionally substituted alkyl, alkenyl, alkynyl, alkoxy, alkenyloxy, alkynyloxy, cycloalkyl or cycloalkoxy group or a -OC(O)R 1 0 group; R 7 represents a hydrogen atom or an alkyl or alkoxy group; X represents an oxygen atom or an NOR group; and R represents a hydrogen atom or an optionally substituted alkyl group.

Good control of phytopathogenic fungi is obtained with a fungicidally effective amount of a compound of formula I wherein R 1 represents a halogen atom or an optionally 15 substituted lower alkyl group; m is an integer of 1 or 3; R 2 independently represents a halogen atom or an optionally substituted lower alkyl group; R 3 represents a halogen atom, an optionally substituted alkyl or alkenyl group, or an optionally substituted amino group; R 5 represents an optionally substituted alkyl, alkoxy, alkenyloxy, alkynyloxy, cycloalkoxy or alkylthio group or R 4 and R 5 may be taken together to represent an optionally substituted alkyleneoxy chain; n is 0 or the integer 1; R 6 represents an optionally substituted alkyl, alkenyl, alkynyl, alkoxy, alkenyloxy, 25 alkynyloxy, cycloalkyl or cycloalkoxy group or a -OC(O)R 1 0 group; R 7 represents an alkyl or alkoxy group; X represents an oxygen atom or NOR group; Y represents an oxygen atom; and R represents hydrogen or C,-Calkyl.

Especially preferred are those formula I compounds in which R 1 represents a halogen atom or C,-Calkyl group; R 2 independently represents a halogen atom or C,-Calkyl group; R represents a halogen atom or an optionally substituted Ci-C4alkyl group; R 4 represents an optionally substituted C1-C4alkyl group; R 5 represents an optionally substituted 8 low er alkyl, alkoxy, alkenyloxy, alkynyloxy or cYcloalkoxy group;

R

6 represents an optionally substituted alkoxy, alkenyloxy, alkynyloxy or cyloalkoxy group Effective control of phytopathogenic fungi may be achieved, for example, with a fungicidally effective amount of one or more of the following compounds: 2.3, 5, -tetraxnethyl-4 5' -trimethoxy-2' -methylbenzophenone; 2, 6-dichloro-4', .5,-dimethoxy-2' -methylbentophenone-0-methyloxime; 2,6dclr-'tbtx-'mtoy2 -methylbenzophenone; 2, 6-dichloro-5' 6' -di-.n-butoxy-4' -methoxy-2 -methylbenzophenone; 2 '-allyloxy-2, 6.dichlor-3' -dimethoxy-6'-methylbenzophenone; 2 '-benzyloxy-2, 6-dichloro-3.,4 '-dimethoxy-6'-methylbenzophenone; 2' -butoxy-2, 6-dichloro-3', -diznethoxy-6 '-methyleve benzophenone; 202' -cyclohexylmethoxy-2 6-dichloro-3, ''.-dimethoxy-6 '-methylbenzophenone;, S* 2' -benzoylmethoxy-2, 6-dichloro-3', 4' -dimethoxy-6' -methylbenzophenone; 2' -cyclopentyloxcy-2 6-dichloro-3' 4' -dimethoxy-6'-methylbenzophenone; 252, 6-dichloro-2', 4' -trimethoxy-6 -methylbenzophenone; 6-dichloro-2 -ethoxy-3' .4,-dimethoxy-6' -methylbenzo- S phenone; 2, 6 -dichloro-2 -heptyloxy- 4 1 -dimethoxy-6'-methyl benzophenone; 2, 6-dichloro-2' -hexyloxy-3' -dimethoxy-6' -methylbenzophenone; 2, 6-dichloro-3' 4 '-dimethoxy-2- 2 -methoxy-ethoxy) -6 methylbenzophenone; 9 2,6dclr- '-iehx- -e 3-e yIbt~y benzophenone; 2. 6-dichloro-3' A4* -dimethoxy-6' -met hyl1-2'- (prop -2-ynyloxy) benzophenone; 2. 6-dichloro-3 -dimethoxy-6 -methyl-2 -pentyloxybenzopheione; 2, 6-dichloro-3 .4 -dimethoxy-6 -methyl-2 -propoxybenzophenone; 2, 6-dichloro-4 -dirnethoxcy-2 -methylbenzophenone; 2, 6-dichloro-4 -rethoxy-2 -methyl-5 -(3-methylbutoxy) berizophenoie; 2, 6-dichloro-4 -methoxy-2 -methyl-5 -(prop- 2-ynyloxcy) benzophenone; 2, 6-dichloro-41 -methoxy-2'-methyl-5 (octyloxy) benzophenone; 192, 6-dichloro-4 -methoxy-2 -methyl-5 (pentyloxy) benzophenone; 2, 6 -di chloro -4 '-methoxy -2 -met hyl -5 '-propoxybenzophenone; 2, 6-dichloro-4 -methoxy-2 '-rnethyl-5 I-trimethylsilanylmethoxybenzophenone; 2, 6-dichloro-5 (I1-ethyl -propoxy) -4 -methoxy-2 -methylbenzo- :20 phenone; 6-dichloro-5' -dif luoromethoxy-41 -methoxy-2'-methylbenzophenone; 2, 6-dichloro-5 -ethoxy-4 -methoxy-2'-methylbenzophenone; 2, 6-dichloro-5 -heptyloxy-4 I-methoxy- 2 -me thy lbenzophenone; 2, 6-dichloro-5 -hexyloxy-4 -methoxy-2 -methylbenzophenone; 6dclr-1-sbuoy4I-ehx-'-ehlezpeoe OV.2, 6-dichloro-5' -isobutoxy-4 -nehoxy-2 -methylbenzophenone; 0. '-uoy2, 6-dichlorosorp-4 -methoxy-2 -methylbenzophenone; -cyclohexylmethoxy-2, 6-dichloro-4 -methoxy-2 -methylbenzophenone; 5 -cyclohexcyloxy-2, 6-dichloro-4 rethoxy-2 -methylbenzophenone; *0*0005'-cycloperityloxy-2, 6-dichloro-4 -methoxcy-2 -methylbenzoo phenone; 5'-cyclopropylmethoxy-2,6-dichloro-4'-methoxy-2-methylbenzophenone; or 5'-decyloxy-2,6-dichloro-4'-methoxy-2'-methyl-benzophenone.

Compounds of particular fungicidal use are those compounds of Formula I B.

Cl

CH,

Q

CO

CI R X OCH,

OR'

(I B) wherein Q represents a hydrogen or a chlorine atom; R represents a hydrogen atom, a C 3

-C

8 cycloalkoxy group or a Ci-Cg-alkoxy group optionally substituted with one or more fluorine atoms, or one phenyl, phenoxy, phenylthio or benzyloxy group, wherein the phenyl moiety may be substituted by halogen, C 1

-C

4 -alkyl, C 1

-C

4 -alkoxy, trifluoromethyl or trifluoromethoxy; and R' represents hydrogen or C 1

-C

10 -alkyl optionally substituted with one or more halogen, C 1

-C

4 -alkoxy, phenyl, phenoxy or phenylthio groups, wherein the phenyl moiety may be substituted by halogen, C 1

-C

4 -alkyl, C 1

-C

4 -alkoxy, trifluoromethyl or trifluoromethoxy, with the proviso, that when Q and R represent hydrogen then R' must be other than methyl.

t 11 Preferred compounds of formula I B are those wherein Q represents a hydrogen or a chlorine atom; R represents a hydrogen atom, a C5-C 7 -cycloalkoxy group, a Cl-Cg-alkoxy group optionally substituted by one or more fluorine atoms, or one phenyl, phenoxy, phenylthio or benzyloxy group, wherein the phenyl moiety may be substituted by halogen, methyl, methoxy, trifluoromethyl or trifluoromethoxy; and R' represents hydrogen or C 1

-C

8 -alkyl optionally substituted by fluorine, chlorine, C 1

-C

4 -alkoxy, phenyl, phenoxy or phenylthio, wherein the phenyl moiety may be substituted by fluorine, chlorine, bromine, methyl, methoxy, trifluoromethyl or trifluoromethoxy.

Further compounds of particular value are those compouns of Formula I C.

CH CH *20 "Q

C

CH

3 R OCH, Q' OR' (I C) wherein Q and Q' independently represent a hydrogen atom or methyl group; R represents a hydrogen atom, a C3-Cgcycloalkoxy group or a C 1

-C

8 -alkoxy group optionally substituted with one or more fluorine atoms, a phenyl, S* 30 phenoxy, phenylthio or benzyloxy group, wherein the phenyl moiety may be substituted with one or more halogen, CI-C 4 alkyl, C 1

-C

4 -alkoxy, trifluoromethyl or trifluoromethoxy groups; and R' represents hydrogen or C 1

-C

10 -alkyl optionally.

12 substituted with one or more halogen,

CL-C

4 -alkoxy, phenyl, phenoxy or phenylthio groups, wherein the phenyl moiety may be substituted by one or more halogen,

C

1

-C

4 -alkyl, C 1

-C

4 alkoxy, trifluoromethyl or trifluoromethoxy groups.

Preferred compounds of formula I C are those compounds, wherein Q and Q' independently represent a hydrogen atom or a methyl group; R represents a hydrogen atom, a C5-C7cycloalkoxy group, a C 1

-C

6 -alkoxy group optionally substituted with one or more fluorine atoms, one phenyl, phenoxy, phenylthio or benzyloxy group, wherein the phenyl moiety may be substituted by fluorine, chlorine, bromine, methyl, methoxy, trifluoromethyl or trifluoromethoxy; and R' represents hydrogen or C 1 -Cg-alkyl optionally substituted by one or more fluorine, chlorine, C 1

-C

4 -alkoxy, phenyl, phenoxy or phenylthio groups, wherein the phenyl moiety may be substituted with one or more bromine, methyl, methoxy, trifluoromethyl or trifluoromethoxy groups.

The present invention also provides new benzophenone compounds of formula Ia *x

R

1 3 *(Ia wherein R1 represents a halogen atom, an optionally *substituted alkyl group or a cyano group; m is an integer of (R)n R

R

4

R

(Ia) wherein R 1 represents a halogen atom, an optionally substituted alkyl group or a cyano group; m is an integer of 1 13 2, 3 or 4; R 2 independently represents a halogen atom, an optionally substituted alkyl or alkoxy group or when R' and R' are on adjacent carbon atoms, R 1

R

2 together represent CH=CH-CH=CH- or an optionally substituted alkylene or oxyalkyleneoxy group; R 3 represents a hydrogen or halogen atom, an optionally substituted alkyl, alkoxy, alkenyl, alkylthio, alkylsulphinyl, alkylsulphonyl, cyano, carboxy, hydroxy, nitro, or an optionally substituted amino group; R 4 represents an optionally substituted alkyl or acyl group; R represents a halogen atom, an optionally substituted alkoxy, alkenyloxy, alkynyloxy, alkylthio, cycloalkyl, cycloalkyloxy, trialkylsilyloxy, -ONa, -OK, -OC(O)R 7

-OCHR

8

C(O)R

7

-OC(O)NR

8

R

9 S()2R 8 -OS(0)2NR 8

R

9

(OR

8

)OR

9

(R

8

)R

9

-S(O)R

8 or -S(O)2R 8 group or R 4 and R 5 may be taken together to represent an optionally substituted alkylene or alkyleneoxy chain; n is 0 or an integer of 1 or 2; R 6 independently represents an optionally substituted alkoxy group, a hydroxy group or a -OC(O)R 10 group when attached to adjacent carbon atoms, or R 5 and one R 6 may be 2.0: taken together to represent -CH=CH-CH=CH- or an optionally 20 substituted oxyalkyleneoxy chain; R 7 represents a hydrogen atom or an optionally substituted alkyl, aryl or alkoxy group; R 8

R

9 and R 10 independently represent a hydrogen atom

R

8 9 or an alkyl group, or R and R may be taken together to Srepresent an alkylene chain optionally interrupted by an oxygen or nitrogen atom; X represents an oxygen atom, a S* sulphur atom or an NOR group; X' represents an oxygen or sulphur atom; Y represents an oxygen or sulphur atom or a sulphonyl or sulphinyl group; and R represents a hydrogen 0 atom or an optionally substituted, alkyl, aralkyl, aryl or 0 30 acyl group, with the provisos that when X represents an oxygen or sulphur atom and: 14 when R 1 represents a halogen atom, then (R 2 )m must be other than a halogen atom or no more than one alkyl or alkoxy group.

(ii) when R 1 represents an alkyl group, then R 2 must be other than alkyl; (iii)when m is 1, then R 2 must be other than an alkoxy group; (iv) when R 3 represents an alkenyl group, then R 3 cannot be substituted with an alkoxy or acyl group; when R 3 represents a haloalkyl group, then R 1 and R 2 must be other than a haloalkyl group; and (vi) when Y represents an oxygen atom, then R 3 and R 5 must be other than a hydrogen atom and n must be 1 or 2.

The compounds of formula I can be prepared by conventional methods.

Thus the compounds having formula I (including those of formula Ia) may be prepared by a process which comprises reacting a compound of formula II

R

I

20 zi

(R

2 m

(II)

with a compound of formula III ee

R

3 2 (R 6 n

Y

(III)

wherein R 1

R

2

R

3

R

4

R

5

R

6 Y, m and n are as hereinbefore defined and one of Z1 and Z 2 represents a hydrogen atom and the other represents the group COC1; or one represents a magnesium halide group MgHal, wherein Hal is a halogen, preferably bromine or iodine, atom, and the other represents COC1 or an aldehyde or nitrile group, followed in the last two cases by oxidation or hydrolysis, respectively, and optionally followed by further derivatization.

The starting materials of formula II and III are known products, and may themselves be prepared according to established methods or routine adaptations thereof.

Substituents R 1 to R 9 which are not compatible with the selected reaction conditions may be introduced after formation of the benzophenone. They may be generated by known methods such as subsequent derivatization or substitution of a suitable group or by cleaving off a suitable protecting group.

When one of Z 1 and Z 2 is hydrogen and the other is COC1, the process is a Friedel Crafts reaction and is effected in the presence of a Lewis acid catalyst according to wellestablished procedures. Suitable catalysts include FeC13, 30 AlC13, SnC14, ZnC12, TiC14, SbCI 5 and BF3, which may be in a molar equivalent amount (based on the acyl chloride).

However, it is also possible to use lesser amounts of catalyst at elevated temperatures, suitably under reflux 16 temperatures, preferred catalysts under these conditions being FeC13, 12, ZnCl2, iron, copper, strong sulphonic acids such as F3CSO3H, and acidic ion exchange resins such as Amberlyst® 15 and Nafion®. The preferred catalyst is FeC, in a 0.001 to 0.2 molar ratio at a temperature of about 50 to 180"C. The reaction can be carried out in a solvent inert under the reaction conditions, for example ethylene or methylene chloride, benzene, octane, decane or solvent mixtures, or in the absence of solvent, conveniently by employing one of the reactants in excess, e. g. in the range of 1:5 to 5:1. If AiC1, is being used, the molar ratio is preferably in the range of 0.5 to 2 and the suitable solvents are e.g. methylenechloride or ethylenechloride at a temperature usually between -10 and -70'C. If in the starting material R3 is methyl and R, or one R, represents a group (formula III) ether cleavage is possible to give the 6hydroxy compound which then can be derivatized according to usual methods.

If the compound of formula II represents 2,6-dichlorobenzoylchloride and the compound of formula III is 1,2,3-trialkoxy- 20 5-alkylbenzene, the Friedel-Crafts reaction with AlCl 3 can be used to prepare different products dependent on the reaction conditions. In case of a molar amount of 0.5 to 2 of aluminiumchloride, a temperature of about 0 to 25'C and a solvent such as methylene or ethylene, the ether cleavage takes place in the 6-position (ortho position) of the compound of formula I within about 1 to 20 hours; at a higher temperature (about 40'C) with if necessary longer reaction times (between about 2 and 24 hours) ether cleavage can be performed in the 5-(meta)-position too.

30 The processes described below can analogously be applied to other starting compounds, if desired.

Starting from compounds of formula n2~ '0-alkyl 0-alkyl (Vill) wherein R 2 represent preferably Cl, CH 3 Ris HorO0alkyl and alkyl is preferably methyl, ether cleavage between about 50 and 100 0 C with HBr/acetic acid leads to compounds of f ormula.

0-alkyl S. S

S

*SSSS.

S

20 wherein R' is H or OH.

Starting from a compound of formula NO 2

WX

wherein R1 and R 2 are defided as before, the cleavage of the 0-alkyl group can be carried out with AlC1 3 (0.5-2 mol)

!I

18 in an inert solvent such as methylenechloride at about 0 C to give the corresponding OH compound.

The alkylation of compounds of formula VIII, IX or the ether cleavage product received from X can be carried out according to usual methods.

Compounds of formula IX wherein R' is H can be reacted with an alkylhalogenide (wherein the alkyl moiety may be substituted) in a lower alcohol in the presence of a basic compound such as potassium carbonate at elevated temperatures 60-150°C).

In case of hydroxy groups in other positions (as in VIII, R' OH or in the reaction product received from X) a salt with a metal has to be produced by reacting the hydroxy compound with e.g. potassium hydroxide. The salt is then reacted with an optionally substituted alkyl halogenide in a polar solvent dimethylformamide) in the absence of water.

20 S* Dialkylation of compounds of formula IX wherein R' is OH

S.

:with the same optionally substituted alkyl groups can be carried out starting from the corresponding di-alkali, preferably di-sodium salt, which can be obtained from the dihydroxy compound and sodium hydride in an inert solvent (e.g.

tetrahydrofurane), the salt is then reacted in an inert polar solvent dimethylformamide) with an excess of the optionally substituted alkylhalogenide at a temperature 30

S

3 between about 80 and 1200C.

Dialkylation with a dihalogen compound of formula o Hal-(CH,),-Hal (Hal C1, Br or I; n 1 to 4) leads to cyclisation (compound XI; n as before): Cl

CH,

CO

Cl O O-alkyl

(CH

2

(XI)

The reaction of the dihydroxy compound IX with the 1 dihalogen compound is carried out in the presence of an excess of potassium carbonate and of a small amount of copperoxide as catalyst at temperatures between about 10 and 0 C, preferrably at room temperature.

To prepare acylated compounds a corresponding hydroxy compound, for example of formula XII R' CH, 2 CO S*20e .6 2 R HO 0-alkyl O-alkyl

(XII)

wherein R, and R 2 are Cl or CH 3 is reacted in form of its I. potassium) salt in an inert polar solvent, such as dimethylformamide, with an optionally substituted acid chloride at a temperature between about 10 to 50 0

C.

S Acylation of compounds of formula IX (with R' H)can be carried out by heating that compound with an acid anhydride in the presence or without an inert solvent at temperatures between about 80 and 120 0

C.

For the preparation of compounds of formula XIII, R'

CH,

.CO

52 R 0O-alkyl

R

(XIII)

wherein R represents a t-butoxy group, R' and R 2 are defined as before but preferably represent Cl, the corresponding hydroxy compound (XIII; R OH) is dissolved in an innert solvent, the solution cooled to about 70°C and after addition of a catalytical amount of trifluoromethane sulfonic acid a stream of 2-methylpropene is bubbled into the mixture for 2 to 6 hours. After neutralizing the acid, the resulting t-butoxy compound can be isolated.

A 5-nitro compound of formula XIV SC CH,

CO

S* C -alkyl (XIV) R (R NO 2 can be prepared by nitration of the corresponding compound unsubstituted in the 5-position (R H) with •concentrated nitric acid at about 50 to 100 0

C.

Nitration of compounds of formula XV

CO

0-alkyl CI O-alkyl

(XV)

in the 2-position can be carried out with concentrated nitric acid at about 30 to 60 0

C.

The resulting or otherwise prepared nitro compounds can be reduced to the corresponding amino compounds, e. g. of formula XVI CI

NH,

CO

II O-alkyl CI O-alkyl

(XVI)

2 with excess powdered iron in a mixture of water/acetic acid 20 50:1 at elevated temperature (60 to 100 0

C).

0 Reaction of the amino compounds with excess formic acid at reflux temperature leads to formylation of the amino group.

OO

Compounds of formula XIV can be brominated in

*OS

position when the equimolar amount of bromine g. in trichloromethane) is added dropwise to the solution of the 30 compound in trichloromethane at 10 to 30 0

C.

S

Benzophenothiones X S) can be prepared from the corresponding benzophenones by heating them with phosphorus S S pentasulfide in an inert solvent to reflux temperature for 2 to 10 hours.

When the magnesium halide is reacted with a nitrile, i.e. the other group Z 1 or Z 2 (formulae II, III) represents CN, the immediate reaction product is an imine of formula

IV:

(R

6 )n

R

4

(IV)

This intermediate is readily converted to the desired benzophenone derivatives of formula I wherein X is an oxygen atom by acid hydrolysis, suitably using mineral acids such as 20 hydrochloric or sulphuric.

When magnesium halide is reacted with an aldehyde, i.e.

the other group Z 1 or Z 2 represents CHO, the immediate reaction product is a tertiary alcohol of formula V:

(R

2 )mm This formula V intermediate is readily converted to the desired benzophenone derivatives of formula I wherein X is an oxygen atom by oxidation, suitably using Mn(IV), Mn(VII), Ce(IV) or Cr(VI) derivatives, nitric acid or oxygen in the presence of a catalyst.

Certain oxime derivatives of formula I may be prepared by reacting the appropriately substituted nitrile oxide of formula VI with a suitable o-dimethoxybenzene of formula VII in the presence of aluminum chloride and an inert solvent to form an intermediate and hydrolyzing the intermediate in 0 aqueous acid to give the desired product compounds of Ib.

The reaction is shown in flow diagram I.

FLOW DIAGRAM I

R

C(R

2

N

R

2

(VI)

R3 n(R) 1) AlCl 3

OCH

3 2) HO

OCH

3

(VII)

(R

6

(R

2 m (Ib) For compounds of formula Ib the substituents R 2 R R' and n are as defined hereinabove for formula I and Ia and m is 0 or an integer of 1, 2 or 3. The oximes of formula Ib may be O-alkylated or O-acylated using conventional alkylation and acylation techniques.

The substituents of the benzophenones produced according to the processes of the invention may be derivatized further according to established methods or routine adaptations thereof, such as hydrogenation, acylation, cleavage of ether bonds, alkylation or nitration.

The formula Ia compounds of the invention are excellent fungicides, especially for the control of phytopathogenic fungi in agriculture or related fields. They are useful for the control of powdery mildew diseases, particularly of Erysiphe graminis, Podosphaera leucocricha or Uncinula necator. Due to excellent plant tolerance, the compounds may be used in all cultivation of plants where infection by the controllable fungi is not desired, e.g. small grain cereals, apples, vine. The absence of target crop phytotoxicity at fungus control rates is a feature of the present invention.

The present invention also provides a fungicidal 20.. composition which comprises a compound of formula I or Ia as 20 defined hereinabove and an agriculturally acceptable carrier.

Said composition may contain one or more compounds of the present invention. Preferably, at least one carrier in a composition according to the invention is a surface-active agent. For example, the composition may contain at least two 25 carriers, at least one of which is a surface-active agent.

The compounds according to formula I or Ia may be applied as technical material, however, said compounds are preferably applied as a composition comprising, besides the formula I or Ia compounds, adjuyants and auxiliaries which 30 are known for formulation purposes and are manufactured into e.g. emulsion concentrates, solutions which may be sprayed directly or diluted, diluted emulsions, wettable powders, soluble powders, dusts, granulates, microencapsulates by

L

well-established procedures. The form of application such as spraying, atomizing, dispersing, pouring may be chosen like the compositions according to the desired objectives and the given circumstances.

It is contemplated, compounds of formula I or Ia may be formulated or applied, either alone or in combination, with one or more pesticides or plant growth regulants. Pesticides used in combination may be herbicides, insecticides or other fungicides or a combination thereof. When the formula I or Ia compounds are applied in combination with another pesticide or pesticides, they may be applied simultaneously or sequentially. Among the available fungicides which may be used in combination with formula I compounds are 4,6-dinitroo-cresol, benalaxyl, benomyl, captafol, captan, carbendazim, chlorothalonil, copper, cymoxanil, dichlofluanid, dichlone, difenoconazole, dimethomorph, diniconzole, dinocap, dithianon, fenpiclonil, fenpropiomorph, hymaxazol, imazalil, iprodione, isoprothiolane, kasugamycin, mancozeb, mepronil, mercuric oxide, oxadixyl, oxolinic acid, penconazole, 20 propineb, pyrifenox, thiabendazole, thiram, tolclofos-methyl, triadimefon, triflumizole, triforine validamycin A, Svinclozolin, zineb, ziram, and the like.

The fungicidal compositions of the invention may be prepared by well-established procedures, e.g. intensive 25 mixing and/or grinding of the active ingredients with other substances, such as fillers, solvents, solid carriers, and optionally surface-active compounds (tensides) Solvents may be aromatic hydrocarbons, preferably the fractions C 8 to C 1 2 e.g. xylenes or xylene mixtures, 30 substituted naphthalenes, phthalic acid esters, such as dibutyl or dioctyl phthalate, aliphatic hydrocarbons, e.g.

cyclohexane or paraffins, alcohols and glycols as well as their ethers and esters, e.g. ethanol, ethyleneglycol monoand dimethyl ether, ketones such as cyclohexanone, strongly 26 polar solvents such as N-methyl 2-pyrrolidone, dimechyl sulphoxide, alkyl formamides, epoxidized vegetable oils, e.g.

epoxidized coconut or soybean oil, water.

Solid carriers, which may be used for dusts or dispersible powders, may be mineral fillers, such as calcite, talc, kaolin, montmorillonite, attapulgite. The physical properties may be improved by addition of highly dispersed silica gel or highly dispersed polymers.

Carriers for granulates may be porous material, e.g.

pumice, broken brick, sepiolite, bentonite, non-sorptive carriers may be calcite or sand. Additionally, a multitude of pre-granulated inorganic or organic materials may be used, such as dolomite or crushed plant residues.

Suitable surface-active substances may be non-ionogenic, anionic or cationic tensides with good dispersing, emulgating and wetting properties depending on the nature of the benzophenone compound to be formulated. Tensides may also mean mixtures of tensides.

Suitable tensides may be so-called water-soluble soaps as well as water-soluble synthetic surface-active compounds.

Soaps usually are alkali, earth alkali or optionally substituted ammonium salts of higher fatty acids (C10-C20), e.g. the sodium or potassium salts of oleic or stearic acid or of mixtures of natural fatty acids which are prepared, for example, from coconut or tallow oil. Furthermore, methyltaurine salts of fatty acids may be used. However, so-called synthetic tensides are preferably used, especially fatty sulphonates, fatty sulphates, sulphonated benzimidazole derivatives or alkyl aryl sulphonates. The fatty sulphates or fatty sulphonates are normally used as alkali, earth alkali or optionally substituted ammonium salts and have an alkyl moiety of 8 to 22 carbon atoms, whereby alkyl also means the alkyl moiety of acyl residues, such as the sodium or calcium salt of lignin sulphonic acid, of sulphuric acid dodecylate or of a mixture of fatty alcohols prepared from natural fatty acids. This also includes the salts of sulphuric acid esters, sulphonic acids and adducts of fatty alcohols and ethylene oxide. The sulphonated benzimidazole derivatives preferably contain 2 sulphonic acid residues and a fatty acid residue with 8 to 22 carbon atoms. Alkyl aryl sulphonates are, for example, the sodium, calcium or triethyl ammonium salts of dodecyl benzene sulphonic acid, dibutyl naphthalene sulphonic acid or of a condensate of naphthalene sulphonic acid and formaldehyde. Furthermore, phosphates, such as the salts of the phosphoric acid ester of a pnonylphenol-(4-14)-ethylene oxide adduct or phospholipids, may be used.

Non-ionic tensides are preferably polyglycolether S derivatives of aliphatic or cycloaliphatic alcohols, saturated or non-saturated fatty acids and alkylphenols, which have 3 to 10 glycol ether groups and 8 to 20 carbon atoms in the (aliphatic) hydrocarbon residue and 6 to 18 carbon atoms in the alkyl residue of the alkyl phenols.

Other suitable non-ionic tensides are the water-soluble, to 250 ethylene glycol ether groups containing polyadducts of ethylene oxide and polypropylene glycol, ethylene diamino polypropylene glycol and alkyl polypropylene glycol with 1 to 1 0 carbon atoms in the alkyl moiety, the substances normally 2 contain 1 to 5 ethylene glycol units per propylene glycol 25 unit. Examples of non-ionic tensides are nonylphenol polyethoxy ethanols, castor oil polyglycol ether, polyadducts of ethylene oxide and polypropylene, tributyl phenoxy polyethoxy ethanol, polyethylene glycol, octyl phenoxy polyethoxy ethanol. Furthermore, fatty acid esters of polyoxy ethylene sorbitan, such as polyoxy ethylene sorbitan trioleate may be used.

Cationic tensides preferably are quaternary ammonium salts, which have at least one alkyl residue with 8 to 22 28 carbon atoms and, furthermore, low, optionally-halogenated alkyl, benzyl or hydroxyalkyl residues. The salts are preferably halides, methyl sulphates or alkyl sulphates, e.g.

stearyl trimethyl ammonium chloride or benzyl bis(2chloroethyl) ethyl ammonium bromide.

The tensides generally used for compositions of the invention are disclosed in publications such as: "McCutheon's Detergents and Emulsifiers Annual", MC Publishing Corp., Ridgewood, NJ, USA 1981; H. Stache, "Tensid-Taschenbuch", 2nd ed., C. Hanser, Munich, Vienna, 1981; M. and J. Ash, "Encyclopedia of Surfactants", vol. I-III, Chemical Publishing Co., New York, NY, USA 1980-1981.

The pesticidal compositions of the invention may comprise 0.1% to 95%, preferably 0.1% to 80% of at least one compound of formula I or Ia, 1% to 99.9% of a solid or liquid adjuvant and 0% to 25%, preferably 0.1% to 25%, of a tenside.

Exemplary of the compositions of the invention are: Emulsion Concentrates: Active ingredient: 1% to 20%, preferably 5% to Surface-active substance: 5% to 30%, preferably 10% to Liquid carrier: 50% to 94%, preferably 70% to Suspension-Concentrates: .Active ingredient: 5% to 75%, preferably 10% to "*25 SWater: 94% to 24%, preferably 88% to Surface-active substance: 1% to 40%, preferably 2% to Wettable Powder: Active ingredient: 0.5% to 90%, preferably 1% to 30 Surface-active substance: 0.5% to 20%, preferably 1% to Solid carrier: 5% to 95%, preferably 15% to a 29 Dusts: Active ingredient: 0.1% to 10%, preferably 0.1% to 1% Solid carrier: 99.9% to 90%, preferably 99.9% to 99% Granulates: Active ingredient: 0.5% to 30%, preferably 3% to Solid carrier: 99.5% to 70%, preferably 97% to As commodity the inventive fungicidal compositions may preferably be in a concentrated form whereas the end-user generally employs diluted compositions. Said compositions may be diluted to a concentration of 0.001% of active ingredient The doses usually are in the range from 0.01 to 10 kg a.i./ha.

Said compositions may also comprise other auxiliaries such as stabilizers, defoamer, viscosity controlling agents, thickeners, adhesives, fertilisers or other active ingredients to obtain special effects.

For a more clear understanding of the invention, the following specific examples are set forth below. These examples are merely illustrations and are not to be understood as limiting the scope and underlying principles of the invention in any way. Indeed, various modifications of :the invention in addition to those shown and described herein will become apparent to those skilled in the art from the following examples and foregoing description. Such modifications are also intended to fall within the scope of the appended claims. The terms HNMR, CIMS and IR as used in the examples hereinbelow designate proton nuclear magnetic resonance, mass spectrum and infrared, respectively.

Example 1 2.6-Dichloro-4.'5'-dimethoxv-2'-methylbenzophenone (Compound 1) (RI=C1, R 2 =6-C1. R=CH3, R4=CH. R5=OCHI. X=O. Y=O. m=1. n=0) A mixture of 4-methyl-veratrol (76.1 g; 500 mmol), 2,6dichlorobenzoyl chloride (120.4 g; 575 mmol) and iron(III)chloride (0.5 g) is heated with stirring. The reaction starts at 90 oC under formation of hydrogen chloride, the main reaction is complete within 10 min at 95 C. Subsequently, the reaction mixture is stirred for another min at 100 °C and then cooled to 65 Upon addition of methanol (350 ml) Compound 1 begins to crystallize. A water/methanol mixture (1:1 v/v; 300 ml) is then slowly added at 40 OC and the mixture is cooled to room temperature with stirring for 30 min. The solid material is collected by vacuum filtration, three times washed with methanol/water (3:1 v/v; 100 ml each) and dried yielding colorless crystals, 148.6 g, (91.4% y) mp 101.5 0

C.

Example 2 Derivatization of benzophenones A) 2.6-Dichloro-4',5'-dimethoxv-2'-nitro-benzophenone 25 25 (Compound 2) FE=6-C1. R=NO 2 R=CH3, Rs=OCH, X=0, Y=O, m=l. n=0) A portion of 2,6-dichloro-3',4'-dimethoxybenzophenone (6.22 g, 20 mmol), prepared analogously to Example 1, is added within 15 min into nitric acid 40 ml) which is 30 Sheated to 40 OC. The clear solution is stirred for 10 min at 40 then 1 h at room temperature. The reaction mixture is then poured into water whereupon a slowly solidifying oil 31 forms. This material is dissolved in a small amount of N,Ndimethyl formamide under warming, then methanol is added and the mixture is chilled and filtered giving Compound 2 as yellow crystals, 5.57 g, (78% y) with mp 143 0

C.

B) 2'-Amino-26-dichloro-4',5'-dimethoxvbenzophenone (Compound 3) R'=6-C1, R'=CF, Rs=OCH, X=O, Y=O, m=l, n=0) A portion of 2 6 -dichloro-3',4'-dimethoxy-2'-nitrobenzophenone (Compound 2; 3.56 g, 10 mmol) is added to a mixture of water (50 ml), glacial acetic acid (1 ml) and powdered iron (3.30 g, 60 mmol) within 15 min at 70 The reaction mixture is stirred at 95 "C for another 3 h. After cooling, toluene (50 ml) is added and the solid material removed by vacuum filtration. The filter cake is washed with toluene. The filtrate and washings are combined and washed with water, dried and then applied onto a flash chromatography column (silica gel, 50 The column is consecutively eluted with toluene, and toluene containing 1%, 5% and 10% of acetone (250 ml each). The fraction eluted by 10% acetone is concentrated in vacuo to a final volume of 10 ml whereby Compound 3 crystallizes yielding yellow crystals, 1.61 g, (49% y) inp 181 OC.

C) 2,6-Dichloro-4',5'-dimethox-2'-formvlamino-benzophenone (Compound 4)

(R

1 =Cl. R 2

R

3 =NHCHO. R=CH3, R5=OCH, X=O. Y=O, m=l, n=0) A mixture of 2'-amino-2,6-dichloro-4',5'-dimethoxybenzophenone (Compound 3; 0.82 g, 2.5 mmol) and formic acid ml) is heated at reflux temperature for 24 h, and evaporated in vacuo. The residue is dissolved in a small a o..

amount of toluene, Compound 4 crystallizes upon addition of cyclohexane giving colorless crystals, 0.64 g, (72% y) with mp 152*C.

D) 2 ,6-Dichloro-5'-hvdroxy-4 -methoxv-2'-methvlbenzophenone (Compound

(R

1 Cl. R2=6-C,. R=CH. R4=CH3. R5=OH X=O, Y=O0 m=l, n=0) A mixture of 2,6-dichloro-4',5'-dimethoxy-2'-methylbenzophenone (Compound 1; 2.5 g, 7.7 mmol), hydrogen bromide/acetic acid 10 ml) and glacial acetic acid ml) is stirred for 1.5 h at 75 0 C, poured into water (100 ml) and twice extracted with dichloromethane (50 ml each). The extracts are combined, dried, and concentrated in vacuo. The resulting oil is applied onto the top of a flash chromatography column (silica gel, 30 Elution is carried out with toluene and toluene/acetone, 9:1 (500 ml each). The fractions containing the material with an Rf 0.54 (silica gel; toluene/acetone, 9:1) are combined and the solvent is evaporated in vacuo until a final volume of 20 ml is reached.

The solution is then extracted three times with aqueous sodium hydroxide (2 N; 30 ml each) The aqueous layer is acidified with hydrochloric acid (6 M) and the precipitate is collected by vacuum filtration and dried to give Compound 25 as colorless crystals, 1.1 g, (45.9% y) mp 152 "C.

E) 2,6-Dichloro-4'-methoxv-2'-methvl-5h-propoxy-benzo- Dhenone (Compound 6)

(R

1 =C1, R 2 =6-Cl, R 3 =CH3 R4=CH3, R 5 =0-n-C3H7, X=O, Y=O, m=l, 30 n=0) A mixture of 2,6-dichloro-5'-hydroxy-4'-methoxy-2'methylbenzophenone (Compound 5; 1.0 g, 3.2 mmol), n-propyl bromide (0.5 g, 4 mmol), potassium carbonate (2.8 g, 20 mmol) 9 and ethanol (10 ml) is stirred for 6 h at 80 0 C, filtered and the filtrate is evaporated in vacuo. The residue is applied onto a flash chromatography column (silica gel, 30 g).

Elution with toluene (750 ml) yields Compound 6 as a brown oil, 800 mg, (70.7% y) which slowly crystallizes (mp 73- 0

C)

F) 2,6-Dichloro-4',5'-dimethoxy-2'-methyl-benzophenthione (Compound 7)

(R

1 =Cl. R 2 =6-C1, R3=CH3. R 4 =O-CH, R5=O-CH. X=S. Y=O, m=l.

n=0) A mixture of 2,6-dichloro-4',5'-dimethoxy-2'-methylbenzophenone (Compound 1; 3.25 g, 10.0 mmol), phosphorus pentasulphide (2.22 g, 10.0 mmol) and toluene (50 ml) is stirred at 110°C for 5 h, treated with p-dioxane, stirred at 100 0 C for a further 24 h. The supernatant is decanted from black, tarry reaction products, silica gel (15 g) is added and the solvent is evaporated in vacuo. A flash chromatography column is packed with silica gel (100 g) and the charged silica gel is layered on top of it. The column is subsequently eluted with petrol ether/acetone (500 ml, 98:2, v/v) and petrol ether/acetone (750 ml, 95:5, v/v) yielding Compound 7 as a dark green oil 40 mg, y), o; 25 which slowly solidifies. When the oil is triturated with cyclohexane three times, it gives a solid, mp 142 0

C

Example 3 Using essentially the same. procedures described 30 hereinabove for Examples 1 and 2 and employing standard derivatization techniques where appropriate, the following compounds are prepared and shown in Table I.

S* R I R 3 0 R 6 R 2

RI

R Table I Comnp 34 s 6O No. RRRR R R R Y MpC 8 Cl 6-Cl H CH3 CH3 0C2H5 H 087 9 CI 6-Cl H CH3 C2H5 OCH3 H 0 106 Cl 6-Cl H CH3 CH3 Cl H 0 168 11 Cl 6-Cl 3-N02 CH3 CH3 OCH3 H 0 oil 12 Br H H CH3 CH3 OCH3 H 0 67 13 Cl 6-Cl H CH3 CH3 OC(0)C2H5 H 0 142-145 14 Cl 6-Cl H CH3 CH3 H H 0 89 1 H H CH3 CH3 OCH3 H 0 66-68 16 Cl 6-CH3 H CH3 CH3 OCH3 H 0 56 17 Cl 6-CH3 H F CH3 OCH3 H 0 18 (CH=CH), 6-Cl CH 3 CH, 0CH3 H 0 19 1 3-I 5-1 CH3 CH3 0CH3 H 0 oil Br 5-Br H CH3 CH3 OCH3 H 0 oil 21 Cl 4-N02 H CH3 CH3 OCH3 H 0 126-128

CVC

R I R 3 0 R 6

R

R Table I No.

22 23 24 26 27 28 Cl Cl Br Cl Cl cl Cl Cl CF3 Cl 6-Cl 6-Cl 6-C1 6-Cl 5-OCH3 5-Br 6-Cl 5-Cl 6-Cl 6-Cl 5-CF3 6-Cl

RH

H

H

H

H

H

H

H

H

H

H

RH3 CH3 CH3

CH

3 CH3 CH3 CH3 CH3 CH3 CH3 CH3 R 5 SCH3 OCH3 CH 20

I

OCH 3 OCH3 OC CH- (CH3) 2 OCH3 Cl OCHF2 OCH3

H

H

2-OCH3

H

H

H

H

H

H

H

H

H

3-OCH3 Mp 0

C

105 92 142 oil 94-96 132-135 oil 126-128 98-101 100-125 a a. a a.

R I R 3 0 R2R 6 bR2 Table I Comp 22 4R yMpO No. RR R R R R' R 0 167 34 Cl 6-Cl H CH3 CH3 OC(O)C-H016 (CH 3) 3 Cl 6-Cl H CH3 H OH H 0 201-203 36 Cl 6-Cl H SCH3 CH3 OCH3 H 0 185 37 Cl 6-Cl H S(02)CH3 CH3 OCH3 H 0 163 38 Cl 6-Cl H CH3 CH3 CH3 3-CH3 0 78 39 Cl 6-Cl H S(O)CH3 CH3 OCH3 H 0 178 .Cl 6-Cl H CH3 CH3 OCH2CH=CH H 0 oil 2 41 Cl 3-Cl 5-Cl CH3 CH3 OCH3 H 099-101 42 Cl 6-Cl H CHI (CH2)20 H o oil 43 Cl 6-Cl H CH3 CHF2 OCHF2 H 065-68 44 CF3 6-CF3 H CH3 CH3 OCH3 H 0 105-107 Cl 6-Cl H CH=CH2 CH3 OCH3 H 0 y R R Y Mp cc Table I Comp No. RRRRR 6-F 3-Cl 6-Cl 6-C1 6-C1 4-Cl 6-Cl 6-Cl 6-Cl 6-Cl 6-Cl 6-Cl 6-Cl 6-Cl

H

H

H

H

H

5-Cl

H

H

H

H

H

H

H

H

CH3 CH3 CH3

CH=CH-CN

CH3 CH3 CH 3 CH3 CH3 CH3 CH3 CH 3 CH3 CH3 CH 3 CH3 C2H5 CH3 CH3 CH3 CH3 CH3 CH 3 CH 3 CH 3 CH3 CH3 CH3 OCH3 OC 2H 5 OC 2H 5 OCH 3

OCH

3 OCH3 C0H9-1.

09-a 0C4H9-j

H

OCH2C6H5 OC5Hllfl OC3H7ji OCH 3

H-B

H

H

H

3-B

H

H

H

H

2 -OH 0 0 0 0 0 0 0 0 0

S

0 0 0 0 97 77 86 160 124 51 oil 119-121 46-48 oil 161 V. R y R Table I Comp4 No. R RRRR6Y Mp OC Cl 6-Cl H CH3 CH3 OCH2C(O)- H 0 105-108 0C2H5 61 Cl 6-Cl H CH3 CH3 H 2-OCH3 0 135 62 cl 6-Cl H CH3 CH3 OCH3 2-0C2H5 0 72 63 Cl 6-Cl H CH3 CH3 Cl H S 64 Cl 4-C1 6-Cl CH3 CH3 OCH3 H 0 108-109 Cl 6-Cl H CH3 CH3 Br H S 66 F 6-F H CH3 CH3 OCH3 H 0 75-77 67 Cl H H CH3 CH3 OCH3 H 0 oil 68 Cl 4-Cl H CH3 CH3 OCH3 H 0 oil 69 Cl 6-Cl H CH3 CH3 CH3 H 0 135-138 Cl 6-Cl H CF3 CH3 Br H 0 71 Cl 5-Cl H CH3 CH3 OCH3 H 0 100-102 72 Cl 6-C1 H C2H5 CH3 0CH3 H 0 oil .t iR P3 0 R 6 R 2j -R 4 P y R Table I Comp No.

73 74 76 77 78 79 81 82 3-C1 6-C1 6-CF3 6-C1 6-F 6-Cl 6-Cl 6-C1 6-Cl 6-Cl 6-Cl 6-C1 CH3

CN

CH3 CH 3 CH3 C3H7 -1 CH3 Br CH3

H

CH3 RH3 CH3 CH3 CH 3 CH3 CH 3 CH3 CH3 CH3 CH3 CH3

H

RCH3 OCH3 OCH3

OCH

2

CN

OCH3 OCH j OCH 3 OC (0)CH3 OCH3 OCH2C=ECH

H

H

R

H

H

H

H

H

H

H

H

H

3-OCH3' 3, 6-di- CH3 V y 0 0 0 0 0 0 0 0 0 0 0 0 Mp 0

C

oil 120 oil 127 72-73 101 72 156-159 124 87 127 122 4 R 4 R Table I No. R Cl 86 cl CH3 Cl Cl Cl Cl

OCH

3 Cl Cl Cl 6RCl 6-Cl 6-CH3 6-Cl3 6-Cl 6-Cl 6-Cl 6-OCH3 6-Cl 6-Cl 6-Cl 6-Cl CH3 CF3

H

H

H

OCH 3 CH3 CR3

COOH

CH3 CH3 CH3 CH3 2,6- C12C6H3 CR3 CR3 CH 3 CH3 CH3 CH3 CR3 CH3 CH 3 CR3

H

H

H

H

Br OCH3 OC H OCH3 OCH3 S 2CH3 SOCH3 C7Hl5 3, 6-di- CR3

H

3 -OCH3 3-Br 3 -OCH3

H

H

H

H

H

H

H

Mp 0

C

i11 186 84 129 140 124 156 113 174 233 227 oil 96 Cl V. S~ 4'

R

Table I Comp No. R 4 R R RRRR6y Mp 0

C

97 Cl 6-Cl H CH3 CH3 0,.C8H17 H 0 oil 98 Cl 6-Cl H CH3 CH3 0..ClOH2l H 0 oil 99 CH3 4-CH3 6-CH3 CH3 CH3 OCH3 H 0 74 100 Cl 6-Cl H CH3 CH3 OCH2-c- H 0 oil 101 Cl 6-Cl H CH3 CH3 OCH2-c- H 0 108 C6Hll *102 ci 6-cl H CH 3

CH

3 0(CH2)2- H 0 oil CH (CH3) 2 103 Cl 6-Cl H CH 3

CH

3 OCH2CH=C H 0 oil -(CH3)2 104 CH3 6-CH3 H CH 3

CH

3 0CH3 H 0 90-92 105 Cl6cHCHCHOCC9 H0oi 16 Cl 6-cl H CH 3

CH

3 Oc-C6Hll H 0 oil .l 6aC H CH *H OcC I H 0 oil R I R 3 4 Table I Comp No.

107 108 109 6-Cl 6-Cl 6-Cl 6- Br 6-Cl 6-Cl

.H

6-Cl 6-Cl 6-C1 6-Cl

H

CH3 f 2)

CH

3

CH

3 OCH 3 CH3

CH

3 NH-CH3

OH

CH3

CH

3

CH

3

CH

3

CH

3

CH

3

CH

3

CH

3 ONa OSi (CH3) OCH 3

OK

Br OCH 3

-CH

2 0-

H

H

2-OCH3

H

2-OCH3

H

H

H

H

Mp 0

C

155- 157 glass oil 102 98 183 76 98 163 oil OCH3 OCH 3 OCH2 Si (CH3) 3 OCH 3 0 62-64 s* 0 L. so 0.0 0 0 0* 0 0 0 0 00 0 0 R I R 3 0 R 26 R y ,R4 R Table I Comp No.

119 120 121 122 123 124 125 126 127 128 129 130 R 3 3-Cl 4-Cl 6-F 5-Cl 6-Cl

H

H

6-Cl 6-Cl 6-Cl 6-Cl 6-Cl

H

6-Cl

H

H

H

H

H

H

H

H

H

H

R

I

CH

3

CH

3

CH

3 OCH 3 OCH3

CH

3

CH

3

CH

3

CH

3

CH

3 CH3 RH 3

CH

3 CH 3

CH

3

CH

3

CH

3

CH

3

CH

3

CH

3

CH

3

CH

3

CH

3 R 5 OCH3 OCH3 OCH3 OCH3 CH 3 OCR 3 OCH 3 Ofl-C6H13 OCH3 OCH3 OCR 3 OCR 3 R'6 2-OCR 3

H

H

H

6-OCH3 2 -OCH3

H

H

2O1- C 3H7 2OfR-C7Hl5 20a- ClOH21 2-OC CH3 y Mp 0

C

0 oil o 126 o 84 0 oil o 115 0 oil 0 34 o oil o 46 o oil o oil R I R 3 0 R 6 R 2 R y R Table I

CR

3

CR

3

CH

3

CH

3 Comp No.

131 132 133 134 135 136 137 138

R-CI

6-Cl 6-Cl 6-Cl 6-Cl 6-Cl 6-Cl 6-Cl

CH

3

CH

3

CH

3

CH

3

CH

3

CH

3

CH

3

CH

3

CH

3

CH

3

CH

3 CH3 CR 5 OCH3 OCH3 OCH 3

OCH

3 C5H11 20 (CH2) 2 -CHl- (CR3) 2 20CH2- CH=CH2 20CH2C=-CH 20c-C5H9 60CR 2- 2 0n- C12H25 20CH2 C-C6H1 1 Mp 0

C

oil 101 73 123 89 oil 88 a a *a a a. a a. a a.

a a a aa* a..

a.

a a. a.

a..

a a a a.

a a a a a a a.

a Comp No.

139 140 141 142 143 144 14S 146 6RCl 6-Cl 6-Cl 6-Cl 6-Cl 6-Cl 6-Cl 6-Cl R 1 R 3 0 R 26 Table I RH

RH

3

CH

3 CH 3

CH

3

CH-

3

OCH

CH

3

CH

3

OCIH

CH

3

CH

3

(C

CH

3

CH

3

(C

CH

3

CH

3

O(C

CH3 CH 3 0O(C OCH 3 -C12 H 2 5 2C N C2H5) 2 [2C(0) N H2 )CH 3

)CH-

2H5) 2 H2) 2-

OH

H2) 3-

OH

20fl- C6H13

H

H

H

20 (CH2) 2 OCH3

H

H

H

y 0 0 0 0 0 0 0 0 Mp 0

C

oil oil 97 136 84 oil 87 86 CC CC CC Ce Ci C e C a C C CC C C. C *e C C C C C I C*C CCC CCC C CC* 4 Comnp No.

147 148 149 150 151 6-C1 6-Cl 6-Cl 6-Cl R Table I RH 3

CH

3

CH

3

CH

3

CH

3

CH

3

CH

3 CH3 OCH2 -P- C6H4-CH3 OCH2 -P- C6H4- C (CH3) 3 OCH3 o (CH2) 20C H3 OCH2 morpholid e R 6

H

H

2OCH2C (0) morphol id e

H

H

Mp 0

C

oil 119 oil oil 163 4. .4 4. 4* 44 4 4 4 4 S *S 4 @4 4 P04. 4.

4. 444 4 *44 404 444 -44 *4 44 4 44 44 044 -44 0 444 .44 4 4 4 9 @4 44 0 4 4..

40 4 40 4 4 4 4 0* 0 t R j R 2.

R Table I Comp No. RS 5R6Y Mp 0

C

152 cl 6-Cl H CH 3

CH

3 OCH2-P- H 0 oil C6H4 -OCH3 153 Cl 6-Cl H CH 3

CH

3 O(CH2)30C H 0 oil 154 Cl 6-Cl H CH3 CH- 3 OCH-3 20(CH2)3 0 225 morphol i nyl x HCl 155 Cl 6-Cl H CH 3

CH

3 OCH3 20(CH2)2 0 103 -N(CH3)2x HC 1 156 Cl 6-Cl H CH 3

CH

3 OCH3 20(CH2)2 0 144 2 x HC 1 17 Cl 6-Cl H CH 3

CH

3 OC2H5 2-0CH3 0 68 R 13 0 RR1 R 2 1N 1 -R R y R Table I Comp No.

158 159 R

I

R

I

R 4 6-Cl 6-Cl

CH

3

CH

3

CH

3 CH 3 6-Cl 6-Cl 6-Cl 6-Cl 3 -CH, 6-Cl 6-Cl

CH

3

CR

3

CH

3

CH

3

CHI

CH

3 Cl

CHI

fl-C7H15 n1-C3H7 a-C4H9 CR3

CHI

CH

3

CH

3

CH

3 OCH3 20(CH2)3 Cl OCH3 20(CH2)3 piper idy lx HCl OCH3 H OCH3 H OCH3 H CH(CH3)2 H OCH) 6-OCH, OCH3 6-OCH, OCH3 H 0(CHd) H

COAH,~

Mp 0

C

87 R 4 Comp No.

168 169 M 170 171 172 173 174 175 6-Cl 6-Cl 6-Cl 6-Cl 6-Cl 6-Cl 6-Cl 6-Cl R Table I

CH,

CHI

CHI

CH,

CHI

CHI

CHI

CHI

R 5

OCHC

4

H

4 CF3-p OCH S iC3H5 OC (CH I)) 0CM ,CH,OCH, CH 2

OCM

0 (CHI) 4 Br

OCH,

OCH)

OCHI

R'6

H

H

H

H

H

6-0 (CHI) IN- (CIHS) 2 6-OCH-

(CHI,

6-OCH,CH,

OCH,CH,OCH,

Mp 0 c 115- 117 102 oil oil oil 108 oil 90 R Comp Table I No. R R R 3RR4RRY mp OC 176 C1 6-Cl H CHI CHI OCOCGHC1 2 6-OCH) 0 186-189 -2,6 177 Cl 6-Cl H H CHI OCH, 6-OCH 3 0 97 178 Cl 6-Cl H CHI CHI CHI 6-OCH, 0 106 179 Cl 6-Cl H OCH, CHI OCH, 6-OCH, 0 121-123 180 Cl 6-Cl H CH, CHI NHCOCH) H 0 155 181 Cl 6-Cl H CHI CH-I OH 6-OH 0 182 182 CF) H H CHI CHI OCH) 6-OCH, 0 oil 183 CF, H H CHI CHI OCH, H 0 oil 184 Cl 6-Cl H CHI CHI OC 4 H9- n 6-OCH,-n 0 oil 185 Cl 6-Cl H CH(CH 1) CHI CHI H 0 110 186 Cl 6-Cl H CHI H NO, H 0 170 195 O-CF'-O H CHI CHI OCH, H 0 Example 4 2 -n-Butoxy- 6-dichloro-3' 4 -dimethoxv-6 -methv-lbenzo- Phenone (Compound 187) (R1-Cl, R 2 =6-Cl. R3=CH3, R 4 =CHJ3. R 5 =OCH:3_ R 6 (Mbj~j~ Y=O. m=1. n=1) a) 2. 6-Dichloro-3 .4 -dimethox-2-hydr...6.

methylbenzophenone (Comvound 59) Aluminum chloride (14.67 g, 0.1 mol) 2,6dichlorobenzoyl chloride (20.95 g, 0.1 mol) and a solution of 3 4 ,5-trimethoxytoluene (18.22 g, 0.1 inol) in dichioromethane :(50 ml), are slowly and consecutively added to dichloromethane stirred at 0 0 C, stirred for 1 h at ice bath temperatures and for 16 h at room temperature, and poured into ice. The organic layer is separated, washed with dilute hydrochloric acid and water, dried, and, after addition of silica gel (100 g) concentrated in vacuo. A flash chromatography column is packed with silica gel (400 g) and *the charged silica gel is layered on top of that. Elution with petrol ether/ethyl acetate (90/10, 1 1; 80/20, 1 1; 50/50, 1 1) yields 2,6-dichloro-3 '41-dimethoxy-2'-hydroxy-6'methylbenzophenone, 10.35 g, (30% mp. 161*C.

b) 2. 6-Dichloro-3 -dimethoxv-2'-hvdroxy-6'-meth lbenzophenone, potassium salt (Compound 188) (Rl=Cl. R 2 =6-Cl, R 3 =CH-1. R 4 =Q 5

=OCH

3

R

6 =2-OK, X=O, Y=O, m=1, n=11 A solution of 2,6-dichloro-3 ,4'-dimethoxy-2'-hydroxcy- 6 '-methyl-benzophenone (10.24 g, 30 minol) is dissolved in ethanolic potassium hydroxide (1.98 g, 30 mmol; 85% in ethanol (100 ml) and stirred at 70 *C for 15 min. The solvent is then evaporated in _vacuo. The residue is dissolved in hot ethanol (50 ml) toluene is added and the solvent is evaporated in vacuo giving Compound 188, 11.7 g.

c) 2 '-n-Butoxy-2.6-dichloro-3'.4'-dimethoxy-6'-methylbenzophenone (Compound 187) A mixture of 2,6-dichloro-3',4'-dimethoxy-2'-hydroxy-6'methyl-benzophenone, potassium salt (1.13 g; 3 mmol), 1bromobutane (0.69 g, 5 mmol) and dimethyl formamide' (5 ml) are stirred at 100 0 C for 8 h, and concentrated in vacuo.

The residue is dissolved by shaking with a toluene/water mixture, after separation, the organic layer is collected 'washed with water and dried. After addition of silica gel 10 the solvent is evaporated. A flash chromatography column is packed with silica gel (25 g) and the.charged silica gel is layered on top of that. Elution with petrol ether/ethyl acetate (95/5, 500 ml) gives the title compound, 0.82 g, (69% y) as colourless crystals, mp. 70 0

C.

Example Using essentially the same procedures described in Examples 1, 2 and 4 hereinabove and employing, if required, standard derivativatization methods, the following compounds shown in Table II are prepared (R 6 R 4 Table II comp.

No.

m Rn Y-R' 189 fn190

LM,

191 192 193 194 3, 5, 6-CH)

CHI

3, 5, 6-CH, 3, 5, 6-CH, 3, 5, 6-CH) 3, 5, 6-CH 3

OCH

3 OCH 3

OCH

3

OCH

3 OCH 3

OCH

3 OCH 3 OCH 3

OCH

3

OCH

2

CH

3 CH

OCH

3

CH

2

CH,

OCH

3

H

H

6-OCH 3

H

H

6-OH nl mp Oc 0 103 0 142-144 1 113 0 73 0 1 137 V. :1.

V**

Example 6 2,6-Dichloro-3',4'-dimethoxvbenzophenone oxime (Compound 195) R'=C1; Fe=6-C1; R=H; Y=O; 9=CH3; 9=H; t=4-QOC; R=H A stirred dispersion of anhydrous aluminum chloride (2.93 g, 22 mmol) in methylene chloride at ice-bath temperatures is treated sequentially with a solution of 2,6dichlorobenzonitrile oxide (3.76 g, 20 mmol) in methylene chloride and, dropwise, with a solution of veratrole (3.32 g, 24 mmol) in methylene chloride, stirred for 0.5 hour, allowed to warm to room temperature, stirred for 4-5 hours and poured 10 into a mixture of ice and HC1. The resultant phase mixture is separated. The organic phase is washed with 2 M HC1, treated with silica gel and evaporated to dryness in vacuo.

The residue is placed on top of a column of silica gel and eluted with mixtures of petroleum ether and ethyl acetate *15 10% and 20% pet ether, respectively) to give the title product as a white solid, 1.25 g (19% y) mp 153 0

C.

Example 7 2.6-Dichloro-4', 5'-dimethoxv-2'-methvlbenzophenone rpropyloxime (Compound 196) R'=Cl; =6-C1; F=CH: Y=O; t=CH R'=OCIH; R=CCHCKH, A •stirred solution of 2,6-dichloro-4',5'-dimethoxy-2'methylbenzophenone oxime (1.5 g, 4.4 mmol) in anhydrous tetrahydrofuran is treated with a 60% dispersion of sodium hydride in mineral oil (0.2 g, 4.8 mmol NaH). After the cessation of hydrogen gas evolution, the reaction mixture is treated with n-propyliodide (0.82 g, 5.3 mmol), allowed to stand at room temperature for 12 hours, and diluted with water. The resultant phase mixture is extracted with ethyl acetate. The organic phases are combined and concentrated in vacuo to give a residue. The residue is chromatographed using silica gel and petroleum ether/ethyl acetate, 8/2. to give the title product as a yellow oil, 0.4 g (23.8% y) identified by NMR (67:23, E/Z isomer ratio).

Example 8 2.6-Dichloro4',5'-dimethoxy-2'-methylbenzophenone-O-acetyloxime (Compound 197) R=Cl; K=6-C1; R=OCH,; R=COCH A stirred solution of 2,6-dichloro-4',5'-dimethoxy 2'methylbenzophenone oxime (2.3 g, 6.8 mmol) in anhydrous 10 tetrahydrofuran is treated with a 60% dispersion of sodium

S

hydride in mineral oil (0.3 g, 7.5 mmol NaH). After the cessation of hydrogen gas evolution, the reaction mixture is treated with acetylchloride (0.55 g, 7.5 mmol) at room temperature, allowed to exotherm to 30 0 C, stirred at ambient temperatures for 2 hours, concentrated in vacuo, treated with water, and filtered. The filtercake is washed with water, dried and recrystallized from methanol to give the title product as white crystals, 1.0 g (38.5% mp 158-149 0

C,

identified by NMR (100% E isomer) Exampl1e 9 Using essentially the same procedures described for Examples 6-8 hereinabove the following compounds are obtained and shown in Table III.

OCH 3 Table III Compound No.

mp *C 198 199 200 201 202 203 204

H

H

H

H

CHI

CH (CHO) CM CHCH 2

CH,

oil

H

H

6 -OCH 3

H

H

H

153 60-70 219-220 112-115 117 oil Exm2le10 2. 6-Dichloro-2' .41-t jmethoXy-6' -methYl -ben zophenone A mixture of 3,4,5-trimethoxytoluene (9.11 g; 50 mmol), octane (25 ml) and iron(III)chloride (50 mg) is stirred at 105*C, and percolating nitrogene, 2..G-dichlorobenzoylchloride -a- 57 (12.04g; 57.5 mmol) is added dropwise within 15 minutes. The mixture is kept at 105 0 C and stirred for another 15 minutes.

After cooling to 50°C ethylacetate (50 ml) is added, the mixture shaken twice with 2 N hydrochloric acid, once with water and dried. The ethylacetate is evaporated (70C) and the liquid cooled with stirring. At 50 0 C petrolether (50 ml) is added. The white crystalls formed are sucked off, washed with petrolether and dried. Yield 12.55 g (70.7 mp. 92 0

C.

Example 11 2.6-Dichloro-2'.3'-dihydroxy-4'-methoxy-6'-methylbenzophenone A mixture of 2,6-dichloro-2',3',4'-trimethoxy-6'-methylbenzophenone (1.78 g; 5 mmol) hydrobromic acid (7.5 ml; 30 in acetic acid) and acetic acid (7.5 ml) is stirred at 750C for 2 hours. Water is added and the mixture extracted with methylenechloride. The extract is washed with water and shaken with 2 N sodium hydroxide. The alcaline solution is acidified with hydrochloric acid, the separated compound dissolved in methylenechloride and the solution washed with water. After evaporation of the solvent purification is carried out by chromatography (flash column, filled with 36 g of silicagel; elution with 500 ml of petrolether/ethylacetate v/v) and 250 ml of petrolether/ethylacetate (1:1; the fraction containing the compound is concentrated, the compound crystallized. The yellow crystalls are washed with petrolether and sucked off; 0.64 g (39 y) mp. 1820C.

Examnl e1.2 2' 3 'Di-n-butox..2.6-.dichloro..4emethpy61-methyl_ benzonheripne Sodiumhydride (0.4 g; 60 1; 10 mrnol) is added with stirring to a solution of 2,6-dichloro-2',3'-dihydroxy.4..

:methoxy-61-methyl-benzophenone (1.64 g; 5 mmol) in tetrahydrofurane. The solvent is evaporated and the residue dissolved in 30 ml of dimethylformamide. 1-iodo-n-butane (4.6 g; 25 mmol) is added, the mixture is stirred at 100 0 C for 8 hours and then the solvent is evaporated. The residue is shaken with toluene/2 N hydrochloric acid, the organic layer separated, washed with water and the solvent evaporated. The residue is purified by chromatography (flash column filled with 35 g of silicagel; elution with 500 ml of petrolether containing 2 t of ethylacetate) yellow oil 7 g; 32 t y).

Exanmle13- 7- 2 .6--Dichlorobenzoyl) -10-methoxy-8-methyl-2.3.4.5tetrahydYro-1,-6-benzodioxocin

(R

5

R

6

(CH

2 4 A mixture of 2, 6-dichlorobenzoyl-2',3' -dihydroxy- 4 'methoxy-6' -methyl-benzophenone 27 g; 10 mmol) potassium carbonate (4 g) copper (II) oxide (50 mg) 1, 4-dibromobutane (2.38 g; 11 mmol) and dimethylfornamide (25 ml) is stirred at room temperature for 15 hours. Water is added and extracted twice with ethylacetate. The ethylacetate phase is washed with water, the solvent evaporated. The residue is purified by chromatography (flash column filled with silicagel, elution with petrolether/ethylacetate 2; v/v) From the enriched fractions the product can be crystallized with methanol. White crystalls (0.56 g; 14.7 mp. 103- 104 0

C.

Example 14 2.6-Dichloro-3'.4'-dimethoxy-6'-methyl-2'-phenylacetoxybenzophenone 10 2,6-Dichloro-3'4' -dimethoxy-2' -dihydroxy-6'-methylbenzophenone (3.41 g; 10 mmol) are added to a solution of potassium hydroxide (0.66 g; 85 in methanol (30 ml). The methanol is evaporated, the residue is dissolved in dimethylformamide (30 ml), phenylacetylchloride (1.70 g; 11 mmol) is added and the mixture is stirred for 15 hours. Then water is added and the mixture is extracted three times with ethylacetate. After evaporation of the solvent methanol is added to the residue to give white crystalls (1.95 g; 42.5 mp. 106 0

C.

Example 2.6-Dichloro-5'-difluoromethoxy-4 '-methoxy-2'-methylbenzophenone To a solution of 2,6-dichloro-5'-hydroxy-4'-methoxy-2'methyl-benzophenone (1.0 g; 3.2 mmol) in dimethoxyethane (7 ml) a solution of sodium hydroxide (0.6 g; 15 mmol) in water (1 ml) is added. The mixture is-heated to 60 0 C with stirring, then a stream of chlorodifluoromethane is introduced for minutes. After further stirring for 1.5 hours the solvent is evaporated. The residue is extracted with a mixture of trichioromethane and water. The organic phase is separated, dried and the solvent is evaporated. For purification, a flash column with silicagel (30 g) is used (elution with mixtures of petrolether/ethylacetate 9:1, then 8:2, then 7:3 The resulting compound forms white crystalls 6 g; 51.8 y) mp. 126-128 0

C.

ExampIl 1 102. 6- D ichl oro 5 D ro i onyl oxy -4'1 -me thoxy -2 'me thyl benzophenone A mixture of 2.6-Dichloro-5'-hydroxy-4'-methoxy-2 methyl-benzophenone and propionic acid anhydride (5 ml) is is1 stirred at 100WC for 5 hours. Toluene/water is added. The organic phase is dried and evaporated. The residue is purified by chromatography (flash column with silicagel g) elution with toluene) The toluene is removed. After treatment with cyclohexane the residue forms white crystalls; 0.5 g (42.6 t y) mp. 142-145 0

C.

ExalIle17 2. 6-Dichloro-5' -tert-butoxy-4' -methoxy-21 -methylbenzophenone A solution of 2,6-dichloro-5'-hydroxy-4' -methoxy-2' methyl-benzophenone (3.0 g; 9.6 mmol) in 50 ml of me thylenechloride is cooled down to 700C, trifluoromethanesulfonic acid (0.3 ml) is added, then a stream of 2-methyipropene (5.5 g; 100 mmol) is introduced within 4 hours. Triethylamine (1.2 ml) is added, the temperature goes up to 200C. The solution is shaken twice with diluted sodium hydroxide and the solvent is evaporated.

The residue is purified chromatographically (flash column with 30 g of silicagel, elution with toluene/acetone 20:1 The residue is treated with petrolether to give 0.7 g of white crystalls (20 mp. 1020C.

Example 18 2. 6-Dichloro-4' -methoxv-2' -methyl-5' -phenoxy-benzophenone A mixture of 2-methoxy-4-methyl-diphenylether (2.1 g; mmol), 2,6-dichlorobenzoylchloride (2.5 g; 12 mmol) and S. iron(III)chloride are heated to 100 0 C with stirring for 4 15 hours. After cooling down the mixture is shaken with toluene/water. The organic layer is dried and the solvent is evaporated. The residue is purified by chromatography (flash column filled with 30 g of silicagel, elution with toluene/petrolether 1:9, changing to 1:1 The residue after evaporation crystallises when treated with diisopropylether; white crystalls (1.5 g; 39 mp.

S113.5 0

C.

Example 19 2.6-Dichloro-4'-methoxy-2'-methyl-benzophenone A mixture of 2,6-dichlorobenzoylchloride (5.24 g; mmol), 3-methylanisole (2.44 g; 20 mmol) and iron(III)chloride (20 mg) is heated to 100 0 C for 45 minutes with stirring. After cooling, toluene is added, the mixture 62 is shaken with water, the organic phase is dried and the solvent is evaporated. The reaction product is purified chromatograpically (flash column with 70 g of silicagel; elution with petrolether/toluene changing from 75:25 to 40:60 After evaporation the residue from the main fraction is treated with petrolether to give white crystalls (1.33 g; 22.5 mp. 89 0

C.

Example 0 5' -Bromo-2. 6-dichloro-4' -methoxy-2' -methyl-benzophenone A solution of bromine (0.25 ml in 3 ml of trichloromethane) is added dropwise to a stirred solution of .15 2 ,6-Dichloro-4'-methoxy-2'-methyl-benzophenone (1.5 g; 5 mmol in 5 ml of trichloromethane), followed by 15 minutes of stirring at 20 0 C. The mixture is shaken with water, sodium hydrogencarbonate solution and water. The organic phase is dried and evaporated. The residue is purified by 20 chromatography (flash column filled with 30 g of silicagel, elution with petrolether/ethylacetate changing from 20:1 to 9:1, 8:2, 7:3 After evaporation, the residue crystallises when treated with petrolether/toluene to give white crystalls (0.45 g; 24 mp. 159 0

C.

Example 2.6-Dichloro-5' -nitro-4' -methoxy-2 'methyl-benzohenone 2,6-Dichloro-4'-methoxy-2'-methyl-benzophenone (0.75 g; mmol) is added to nitric acid (10 ml; The mixture 63 is stirred at 80°C for 1 hour. After addition of water the reaction product crystallises and is chromatographically purified (flash column filled with 30 g of silicagel, elution with toluene). White crystalls (0.35 g; 41 mp. 156- 1600C.

Example 21 ::10 2.6-Dichloro-4'-hydroxv-5'-nitro-2'-methyl-benzophenone 10 Aluminumchloride (1.5 g; 11 mmol) is added to a solution of 2,6-dichloro-5'-nitro-4'-methoxy-2'-methyl-benzophenone (1.8 g; 5.3 mmol) in methylenechloride (6 ml). The mixture is stirred for 30 minutes at 20°C and for 1 hour at 45 0 C, 5 ml 15 conc. hydrochloric acid/ice are added. After shaking with ml of methylenechloride the organic layer is treated with 2 N hydrochloric acid and with water. After drying the solvent is evaporated, the residue purified by chromatography (flash column filled with 30 g of silicagel, elution with toluene) 20 The residue from the main fraction is treated with diisopropylether to give yellow crystalls; (1.2 g; 73 y); mp. 170°C.

The compounds of Tables IV to X can be prepared analogously to the examples described hereinbefore.

64 Compounds of formula cI c

CH

3 3 R No. R 5 mp. (C]c 1 O-C 6

H

5 113.5S 2 Br 159 3 N02156 :4

O-CH

2 -CONI{-(4-0CH 3

-C

6

H

4 154

O-CH

2

-CONH-C

6

H

5 133 6 O-CH 2

-CONH-CH

2

-C

6

H

5 150 *7 O-CH2-(2-pyridyl) 114 8 0-CU 2 (3-pyridyl) 119 9 0-CU 2 (4-pyridyl) 142 *C I

S

O-CHi- 2 N13 11 0-(CH 2 4 -0-C 6

H

5 86-9 OCH 3

S

O-CH 2OCH 3 12 N124 Compounds of formula Cl coCH 3

~CH

3 No. R 5 rp. 1 0

C]

1 O-C 6

H

5 113.5 2 Br 159 3 N0 2 156-60 *4

O-CH

2 -CONH-(4-OCH 3 -C6H 4 154

O-CH

2

-CON'H-C

6

H

5 133 6 O-CH 2

-CONH-CH

2

-C

6

H

5 150 7 O-CH 2 (2-pyridyl) 114 8 O-C11 2 -(3-pyridyl) 119 9 0-CH 2 (4-pyridyl) 142 0C 2 N 134 11 O-(CH 2 4

-O-C

6

H

5 86-9 OCH 3

S

O-CH

2

OCH

3 N 3 19 124 Table IV continued a a a.

a.

a. a.

a a a a. a.

a. a.

a a.

S

O-CH

2 CF F

N-

0-CH 2 164 Compounds of formula

S.

S. S Sc *55555

S

*5555* 1 CH 3 0 0-CH 3 mp. 0

CI

No.

3 -CH 3 5-CH 3

S-CM

3 4, 6- (CM 3 2 82 oil 89 142 Table VI Compounds of formula 0*

S

S

S. S

SS

S

55555S

S

S

S

-CH3 No.

mp. [OC] CH2- C (C3)2

CH

2

-C(C

2

H

5 2 CH2 -CH 3

-C

6

H

4 CH2-(3-C11 3

-C

6

H

4 CH2 -CH 3

-C

6

H

4 CH2 -Cl -COO 4

CH

2 (4 -N0 2

-C

6

H

4 CH2-(4-F 3

CO-CGH

4

CH

2 (4-CN-C 6

H

4

N

CH

2 0-

CH

2 (3-CH 3

O-C

6

H

4

CH

2 (4-H 2

NCO-C

6

H

4

CH

2 (4-CH 3

O-C

6

H

4

H

105 73 88 92 121 178 120 189 119 oil 106 77 161 69

CH

2

-CO-C

6

H

5 84 No. R mp. 0

C]

16 CH 2 -C1{=CH-C 6

H

5 oi) 17 H 2 -(4CO 2

H

3

-C

6

H

4 106 18 CH 2

-CH

2

-CH

2

-C

6

H

5 79 19 CH 5 -(CH- 3 2 -C 6

H

3 86

CH

2

(CH

3 2

-C

6

H

3 125 .21 CO-CH 2

-C

6

H

5 106 22 CH 2 -(2-naphthyl) 84 *23

CH

2

-CH

2

-CH

2 -0-C 6

H

5 79 24 CH 2

-CH

2

-C

6

H

5 110

CH

2

-CH

2

-O-C

6

H

5 oil 26 CH 2 -(2-C1-C 6

H

4 131 :27 CH 2 -(3-Cl-C 6

H

4 124 28 CH 2 (2-F-C 6

H

4 88 29 CH 2 (4-F-C 6

H

4 102

CH

2 (2-CN-C 6

H

4 127 31 CH 2 -(3-FC 6

H

4 88 32 CH 2 (3-pyridyl) 84 *33 CH 2 (2-N0 2

-C

6

H

4 140 *S34

CI{(CH

3

)-C

6

H

5 92

CH

2 -(4-CF 3

-C

6

H

4 125 TAba1IThi Compounds of formula @0 .0 S 600 0 S. 06 0 S

S

0e 0@ 0 SOS S

OS..

S S SO S *0 0 0

SOS,

50

S

6@5i

S

S. S 11 CH 3 mp. 0

C]

gO 0@ 0 0*

S

0 119 123-5 133 103 71 Table VII Compounds of formula 555555 555555 CH 3 No.

mp. 0 c]

H

CH

3

H

H

CMH3 n-C 7

H

1 5 n-C 7

H

1 5 CH2 CH H (H3)2

CH

2

-SC

6

HS

CH2 -S t-C 4 H 9 oil oil 63 Tahl A X Compounds of formula 1 CH3 mp. tOCI o -C 0- CH 2

CH

2 S -C 6

H

5

O-CH

2 -CO-C (CH 3 3

H

H

H

H

CH

3

OH

OH

0-CE 2 -0-CEH 5 n-C 5

E

11

CH

3

CE

3

CE

2

-O-CH

2

-C

6

H

CE

2

-S-CH

3

CH

2 -S0 2

-C

6

H

CH

2

-S-C

6

H

CE

2 -S-t-C 4

H

9

H

CH

3

CE

3 oil 182 Tahl eX Compounds of formula ~CH 3 0 No. mp. (OC] o -CH 3

O-CH

2

-CH

2

-S-C

6

H

5 0-CH 2

-CO-C(CH

3 3

H

H

H

H

0-CH 3

O-CH

2 -0-CH 2

-C

6

H

5 o -CH 2

C

6 H5

H

n-CSH 1 1

CH

3

CH

3

CH

2 -0-H 2

-C

6

H

H2 -S-CH 3 H2 S0 2

-C

6

H

H2-S-C 6

H

CH

2

-S-C

6

H

CH

3

CH

3

OH

Formulations Emulsion Concentrate active compound 200 g/l ethoxylated castor oil 100 g/l tetrahydrofurfuryl alcohol 793 g/l 10 Biological Test Results The fungicidal activity of the compositions and compounds of the invention is investigated by means of the following tests.

a) Activity Against Cereal Powdery MildewEftsiphe craminis f.sp. hordei and f.sp. tritici) This test measures the prophylactic activity of test compositions and test compounds applied as a foliar spray.

20 Cereal seedlings (barley, cv Golden Promise; wheat, cv Kanzler) are grown to the 1 leaf stage. The plants are then sprayed with a solution of test compound in water, made up from a 5,000 ppm stock solution in acetone containing 5,000 ppm of TRITON® X 155 (a non-ionic polyoxyethylene ether surfactant). Plants are treated using an automated spray line with atomizing nozzles. The spray volume is 20 ml. One to three days after treatment, the seedlings are inoculated with powdery mildew by shaking stock culture plants with sporulating pathogen (barley Erysiphe graminis f.sp.

hordei; wheat Erysiphe graminis f.sp. tritici) over them.

Thereafter, the plants are kept for 3h without air movement in order to allow the spores to settle on the leaves. The plants are then kept in the greenhouse until symptoms occur.

Assessment is based on the percentage of diseased leaf area compared with that on control leaves.

b) Activity Against Apple Powdery MildewP(dosphaera leucotriche This test measures the prophylactic activity of test compositions and test compounds, applied as a foliar spray.

Apple seedlings (cv Morgenduft) are grown to the 6-7 leaf stage and then cut back to 3 leaves, taking off the oldest 10 and youngest leaves. The plants are sprayed with a solution (20 ml) of test compound in water, made up from a 5,000 ppm stock solution in acetone containing 5,000 ppm of TRITON® X 155. The plants are treated using an automated spray line with atomizing nozzles. One to three days after treatment, the seedlings are inoculated with powdery mildew by shaking stock culture plants with sporulating pathogen over them.

SThereafter, the plants are kept for 3 h without air movement.

The plants are then kept in the greenhouse until symptoms occur. Assessment is based on the percentage of diseased 20 leaf area of treated plants compared with that of control plants.

c) Activity Against Grapevine Powdery MildewUzicinula necator) This test measures the direct protectant activity of test compositions and test compounds applied as foliar spray.

Cuttings of grapevine (cv Muller-Thurgau) are grown to the 6- 8 leaf stage and then cut back to 4 equally sized leaves.

The plants are sprayed to run-off in a spray cabinet with a solution (20 ml) of test compound in water made up from a 5,000 ppm stock solution in acetone containing 5,000 ppm of TRITON® X 155. Two days after treatment, the cuttings are inoculated with conidia of Uncinula necacor in a special spore setting tower. The spores are blown from freshly sporulating grape leaves necacor stock culture) into the upper hole of the settling tower and are allowed to settle on the leaves for 5 min. Then the plants are kept in a phytotron at 18 0 C night and 22 0 C day temperature at an interval of 12 h night and 12 h day. Illumination is accomplished by fluorescent tubes at 11,200 lux. Assessment is carried out after 21 days by visual inspection and based 1. 0 on the percentage of the diseased leaf area of the three youngest leaves compared with that on control plants.

The results of the tests are set out in Table A and B below, in which the compounds are identified by reference to the preceding Compound Nos. allocated in Examples 1 to 9 above or 15 to their Nos. in Tables IV to X. Absence of a rating indicates that none of the tests described above was carried out. A rating 0 indicates disease as untreated control, a rating 100 indicates no disease.

20 *20 Table A Podosphaera Uncinula Erysiphe graminis leucotricha necator barley wheat Comp.No. 100 ppm 100 ppm 100 ppm 200 ppm *1 100 100 96 84 *2 99 100 0 41 *3 0 0 0 4 95 100 41 94 99 41 6 99 100 *8 100 100 100 Table A Podospha era Uncinula leucotricha necator .4t* a a a a C omp. No.

*9 *10 *11 *12 13 *14 *15 16 17 18 19 21 23 24 26 27 28 29 31 32 33 34 Erys iphe barley 100 ppm 0 85 0 23 87 0 99 100 25 89 19 100 9 100 94 82 90 100 99 99 1 39 0 gramini s wheat 100 ppm 70 100 0 0 100 36 73 94 5 57 26 100 19 100 100 79 100 98 93 100 28 98 0 100 ppm 44 0 0 200 ppm a 0 0 77 73 28 100 53 33 89 97 8 Table A Podosphaera Uncinula leucotricha necator a.

~9 9 a 9. 99 a a 9 9 a 99..

99 @9 a *9 9 9 9.9 a at.

.9 0a S *990 99 9 a.

*0 a a.

9@9*9* Comp. No.

35 36 37 38 39 40 41 43 44 46 47 48 51 52 53 *54 56 *57 *58 *59 62 Erysiphe barley .100 ppm 0 49 70 42 28 100 49 23 89 100 95 84 4 51 0 100 100 100 99 100 0 0 100 gram iri s wheat 100 ppm 22 61 37 77 100 99 49 38 100 100 90 6 0 100 100 100 100 100 1 32 100 100 ppm 9 100 94 200 ppm Table A e.

Comp. No.

*64 *66 *67 *68 *69 *71 *72 *73 *74 76 *77 *78 *79 82 84 86 91 *93 *94 Erys iphe barley 100 PPM 95 0 43 0 0 99 55 99 0 61 33 41 0 0 76 100 0 33 0 93 0 0 91 gramini s wheat 100 ppm 99 0 0 0 28 32 72 94 0 34 57 99 0 100 100 0 28 17 100 17 0 0 Podospha era leucotricha 100 ppm 71 0 0 0 0 0 26 16 0 Un cinfl 1a necator 200tppm 63 33 Table A Podosphaera Uncinula Erysiphe graminis leucotricha necator barley wheat z Comp.No. 100 ppm 100 ppm 100 ppm 200 ppm 0 0# 0 0* 0 *00 0 0000 0 *00*0* *96 *97 *98 *99 *100 *101 *102 *103 *104 *105 *106 *107 *108 *109 *110 *111 *112 *113 *114 *115 *116 *117 100 100 100 86 100 100 100 100 100 100 100 0 100 100 100 95 0 0 0 100 100 100 100 100 100 6 100 100 100 100 14 100 100 21 100 100 100 100 19 28 17 64 100 100 100 100 29 100 87 100 27 100 Table A Podosphaera Uncinula leucotricha necator Comnp.No *118 *119 *120 *121 *122 *123 *124 *125 *126 *127 *128 *129 *130 *131 *132 *133 *134 *135 136 *137 *138 Erys iphe barley 100 ppm 99 100 100 100 100 0 100 100 100 100 100 100 0 100 100 100 100 100 100 100 100 grarninis wheat 100 ppm 13 89 89 100 100 44 100 28 100 100 100 100 78 100 100 100 100 100 100 100 100 100 ppm 66 98 46 37 28 9 89 8 100 100 100 100 0 100 100 100 100 100 100 97 100 200 ppm Table A Podosphaera Uncinula leucotricha necator .i Comp No.

*139 *140 *141 *142 *143 *144 *145 *146 *147 *148 *149 *161 *162 *163 166 167 168 169 170 171 172 173 Erysiphe barley 100 ppm 100 100 97 97 100 100 84 65 100 100 39 48 23 97 100 100 100 100 100 97 100 26 graminiS wheat 100 ppm 100 100 100 100 100 100 97 91 100 100 66 77 4 90 100 97 100 100 100 100 97 53 100 ppm 100 100 0 53 100 100 200 ppm 100 100 7 2 0 100 0 100 0 Table A Podosphaera Uncinula leucotricha necator S S Comp. No.

174 175 176 177 178 180 181 182 183 184 185 186 189 190 191 196 197 199 200 201 202 Erysiphe barley .10 0 ppm 100 100 0 52 100 95 5 100 100 100 0 0 100 98 100 0 71 0 100 98 0 graminis wheat 100 ppm 100 100 0 0 100 19 0 93 74 100 0 100 100 8 100 82 78 0 100 0 92 100 ppm 98 100 8 0 100 200 ppm 6 0 0 100 0 100 100 68 99 87 1 Table A Podospha era Uncinula Ezysiphe graminis leucotricha necator barley wheat Comp.No. 100 ppm. 100 ppm 100 ppm 200 ppm indicates the infection with Erysiphe graminis and Podosphaera leucocricha was carried out 72 h after treatment 0 *0 0 0 0 Compound Table/No.

Erisyphe barley 100 ppm graminis wheat 100 ppm Podosphaera leucotricha 100 ppm IV! 1 2 3 4 100 100 100 51 11 26 100 98 100 100 100 100 100 100 23 100 92 100 100 100 Table B (continued) Erisyphe gramtinis Pdohar Podosphaera Compound Table/No.

barley 100 ppm wheat 100 ppm.

leucotricha 100 ppm 12 96 100 0 13 100 90 0

C

C

V/1 2 3 4 VI"i 2 3 4 6 7 8 9 11 12 VI/13 16 17 18 19 21 100 100 100 100 100 100 100 100 100 100 100 100 74 100 100 100 100 99 100 100 100 100 100 100 100 100 45 100 23 100 100 0 97 63 0 100 100 100 100 100 100 0 100 6 96 100 0 100 100 100 100 100 100 38 100 100 100 100 100 58 100 97 100 100 100 100 100 100 Table B (coninued) Erisyphe graminis Pdopar Podosphaera Compound Table/No.

barley 100 ppm wheat 100 ppm leucotricha 100 ppm a 100 100 100 100 100 100 100 95 100 100 100 100 100 19 100 93 100 100 VII/3 4

IX/

Claims (12)

1. A compound of formula la R X R 3 6 2 (R)n 4 wherein R' represents a halogen atom, an optionally substituted alkyl group or a cyano group; m is an integer of 1, 2, 3 or 4; R 2 independently represents a halogen atom, an optionally substituted alkyl Or alkoxy group or when R' and R 2 are attached to adjacent carbon atoms, R' and R 2 may be taken together to represent an optionally substituted CH=CH-CH=CH or alkylene or oxyalkyleneoxy group; R 3 represents a hydrogen or halogen atom, an optionally substituted alkyl, alkoxy, alkenyl, alkylthio, alkylsulfinyl, alkylsulfonyl, cyano, carboxy, hydroxy, nitro, or an optionally substituted amino group; R 4 represents an optionally substituted alkyl or acyl group; R 5 represents a halogen atom, an optionally substituted alkoxy, alkenyloxy, alkynyloxy, alkylthio, cycloalkyl, cycloalkyloxy group, trialkylsilyloxy group, ONa, OK, OC(O)R 7 OCHRC(O)R 7 OC(O)NRR' 9 S(O) 2 R, OS(0) 2 NR R OP(X')(OR)OR 9 OP(X')(RX)R 9 S(O)R 8 or S(0) 2 R group or R 4 and R' may be taken together to represent an optionally substituted alkylene or alkyleneoxy chain; n is 0, or an integer of 1 or 2; R 6 independently represents an optionally substituted alkoxy group, a hydroxy or an OC(O)R" group or when R' and R" are attached to adjacent carbon atoms, RSR 6 may be taken together to represent CH=CH-CH=CH or an optionally substituted oxyalkyleneoxy chain; R 7 represents a 20 hydrogen atom or an optionally substituted alkyl or alkoxy group; R 8 R 9 and R' 0 independently represent a hydrogen atom or an alkyl group or R and R 9 may be taken together to represent an alkylene chain optionally interrupted by an oxygen or nitrogen atom; X represents an oxygen atom, a sulfur atom or an NOR group; X' represents an oxygen atom or a sulfur atom; Y represents an oxygen atom, a sulfur atom, a sulfonyl or a sulfinyl group; and R represents a hydrogen atom or an optionally substituted alkyl, aralkyl, aryl or acyl group; with the provisos that when X is O or S and: when R' represents a halogen atom, then R 2 must be other than a halogen atom or no more than one alkyl or alkoxy group, (ii) when R' represents an alkyl group, then R 2 must be other than alkyl; (iii) when m is 1, then R 2 must be other than an alkoxy group; (iv) when R 3 represents a substituted alkenyl group, then R 3 must be substituted with other than an alkoxy or acyl group; when R 3 represents a haloalkyl group, then R' and R 2 must be other than a haloalkyl group; and (vi) when Y represents an oxygen atom, then R 3 and R' must both be other than a hydrogen atom and n must be an integer of I or 2. I:\DAYLIB\libc\O 182a.doc 88

2. A compound of formula Cl 0 CH 3 Q C O-CH 3 O R' wherein Q represents a hydrogen or a chlorine atom; R represents a hydrogen atom, a C 3 C8-cycloalkoxy group or a Ci-C 8 -alkoxy group optionally substituted with one or more fluorine atoms or one phenyl, phenoxy, phenylthio or benzyloxy group, wherein the phenyl moiety may be substituted by halogen, Ci-C 4 -alkyl, Ci-C 4 -alkoxy, trifluoromethyl and/or trifluoromethoxy; and R' represents hydrogen or Ci-Clo-alkyl optionally substituted with one or more halogen, Ci-C 4 -alkoxy, phenyl, phenoxy or phenylthio groups, wherein the phenyl moiety may be substituted by halogen, Ci-C 4 -alkyl, Ci-C 4 alkoxy, trifluoromethyl or trifluoromethoxy, with the proviso, that when Q and R :represent hydrogen, then R' must be other than methyl.

3. A compound of formula CH 3 O0 CH 3 II Q' R' I wherein Q and Q' independently represent a hydrogen atom or methyl group; R represents a hydrogen atom, a C3-Cs-cycloalkoxy group or a Ci-C 8 -alkoxy group optionally substituted by one or more fluorine atoms, a phenyl, phenoxy, phenylthio or benzyloxy group, wherein the phenyl moiety may be substituted with one or more halogen, CI-C 4 alkyl, Ci-C 4 -alkoxy, trifluoromethyl or trifluoromethoxy groups; and R' represents hydrogen or CI-Clo-alkyl optionally substituted with one or more halogen, CI-C 4 -alkoxy, phenyl, phenoxy or phenylthio groups, wherein the phenyl moiety may be substituted with one or more halogen, Ci-C 4 -alkyl, Ci-C 4 -alkoxy, trifluoromethyl or trifluoromethoxy groups.

4. A fungicidal benzophenone derivative according to any one of claims 1-3, substantially as hereinbefore described with reference to any one of the examples. A process for the preparation of a compound of formula I If [R:\UBZ]05502.doc:lam S(I) wherein R represents a halogen atom, an optionally substituted alkyl or alkoxy group, a cyano or a nitro group; m is 0 or an integer of 1, 2, 3 or 4; R 2 independently represents a halogen atom, an optionally substituted alkyl or alkoxy group, a nitro group or when R' and R 2 are on adjacent carbon atoms, R' and R 2 may be taken together to represent an optionally substituted CH=CH-CH=CH, alkylene or oxyalkyleneoxy group; R 3 represents a hydrogen or halogen atom, a cyano, carboxy, hydroxy or nitro group or an optionally substituted alkyl, alkoxy, alkenyl, alkylthio, alkylsulfinyl, alkylsulfonyl or amino group; R 4 represents a hydrogen atom or an optionally substituted alkyl or acyl group; R represents a hydrogen or a halogen atom or a nitro group, an optionally substituted alkyl, alkoxy, alkenyloxy, alkynyloxy, alkylthio, cycloalkyl, cycloalkyloxy, hydroxy, aryloxy, Strialkylsilyloxy, ONa, OK, OC(O)R 7 OCHR'C(O)R 7 OC(O)NRR 9 S(0) 2 R 8 OS(O) 2 NRR 9 OP(X)(OR 8 )OR, OP(X')(R 8 )R 9 S(O)R 8 or S(0) 2 R 8 group or R 4 and R may be taken together to represent an optionally substituted alkylene or alkyleneoxy chain; n is 0 or an integer of 1 or 2; R 6 independently represents a halogen atom, an optionally substituted alkyl, alkenyl, alkynyl, alkoxy, alkenyloxy, alkynyloxy, cycloalkyl, cycloalkoxy, hydroxy or OC(O)R 1 0 group or when R 5 and R 6 are on adjacent carbon atoms, R R 6 may be taken together to represent an optionally substituted CH=CH-CH=CH or oxyalkyleneoxy chain; R 7 represents a hydrogen atom or an 20 optionally substituted alkyl or alkoxy group; R 8 R 9 and R 1 0 independently represent a hydrogen atom or an optionally substituted alkyl, aryl or aralkyl group, or, R 8 and R 9 may be taken together to represent an alkylene chain which may be interrupted by an oxygen or nitrogen atom; X' represents an oxygen atom or a sulfur atom; and Y represents an oxygen atom, a sulfur atom, a sulfonyl or a sulfinyl group, which comprises reacting a compound of formula I 1 R 2 z (R with a compound of formula p PRzith a compound of formula 1I1 [R:\LIBZ]05502.doc:lam 3 R 2 6 z (R)h 4 Y R R R (mi) wherein R 2 R 3 R 4 R

5 R 6 Y, m and n are as defined for formula I and one of Z' and Z 2 represents a hydrogen atom and the other represents the group COCI or one represents a magnesium halide group MgHal, wherein Hal represents a bromine or iodine atom, and the other represents COC1.

6. A process for the preparation of a compound of formula Ib OH 1 3 R N R 6 2 (R)n (R(R m o/CH3 .o O S* CH 3 H (Ib) wherein m is 0 or an integer of 1, 2 or 3; R' represents a halogen atom, an optionally substituted alkyl or alkoxy group, a cyano or a nitro group; R 2 independently represents a halogen atom, an optionally substituted alkyl or alkoxy group, a nitro group or when R' and R 2 are on adjacent carbon atoms, R' and R 2 may be taken together to represent an optionally substituted CH=CH-CH=CH, alkylene or oxyalkyleneoxy group; R 3 represents a hydrogen or halogen atom, a cyano, carboxy, hydroxy or nitro group or an optionally substituted alkyl, alkoxy, alkenyl, alkylthio, alkylsulfinyl, alkylsulfonyl or amino group; n .Is. 15 is 0 or an integer of 1 or 2; R 6 independently represents a halogen atom, an optionally substituted alkyl, alkenyl, alkynyl, alkoxy, alkenyloxy, alkynyloxy, cycloalkyl, cycloalkoxy, hydroxy or OC(O)R'O group; and R 1 0 represents a hydrogen atom or an optionally substituted alkyl, aryl or aralkyl group which comprises reacting a compound of formula VI 1 R (RR SVI 7 *th at least one molar equivalent of a compound of formula VII [R:\LIBZ]05502.doc:lam 3 R (R)n OCH3 OCH3 (vII) in the presence of at least one molar equivalent of aluminium chloride and a nonpolar solvent to form an intermediate and hydrolysing said intermediate in the presence of an acid and water to yield the product formula Ib compound.

7. A process for the preparation of a fungicidal benzophenone derivative according to claim 1, substantially as hereinbefore described with reference to any one of the examples.

8. A fungicidal benzophenone derivative prepared by the process of any one of claims 5 to 7. 0o

9. A fungicidal composition which comprises an agriculturally acceptable carrier and a fungicidally acceptable amount of a compound according to claim 1.

10. A fungicidal composition which comprises an agriculturally acceptable carrier and a fungicidally acceptable amount of a compound of formula Id Y R X R 15 (Id) wherein X is an oxygen atom or a group NOR; Y is an oxygen atom; R 2 and R 3 are each independently a halogen atom or a Ci-C 6 -alkyl group, R 4 is a CI-C 6 -alkyl group; R and R 6 are each independently an optionally substituted Ci-C 6 -alkoxy group; m is an integer of 1 or 3 and n is an integer of 1.

11. A fungicidal composition which comprises an agriculturally acceptable carrier and a fungicidally acceptable amount of a compound according to any one of claims 2-4 or 8.

12. A method for the control of a phytopathogenic fungus or a disease .R\aused thereby, which comprises contacting said fungus with a fungicidally effective [R:\LIBZ]05502.doc:lam 92 amount of a compound according to any one of claims 1-4 or 8, or a composition according to any one of claims 9-11. November, 2001 American Cyanamid Company Patent Attorneys for the Applicant/Nominated Person SPRUSON FERGUSON *C I R:\LIBZ]05502.doc: [am