WO2005123698A1 - Fungicides based on nitrogen-containing heterocycles - Google Patents

Fungicides based on nitrogen-containing heterocycles Download PDF

Info

Publication number
WO2005123698A1
WO2005123698A1 PCT/EP2005/006687 EP2005006687W WO2005123698A1 WO 2005123698 A1 WO2005123698 A1 WO 2005123698A1 EP 2005006687 W EP2005006687 W EP 2005006687W WO 2005123698 A1 WO2005123698 A1 WO 2005123698A1
Authority
WO
WIPO (PCT)
Prior art keywords
alkyl
halo
alkoxy
aryl
heteroaryl
Prior art date
Application number
PCT/EP2005/006687
Other languages
French (fr)
Inventor
Patrick Jelf Crowley
Urs Müller
Markus Dobler
John Williams
Original Assignee
Syngenta Participations Ag
Syngenta Limited
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Syngenta Participations Ag, Syngenta Limited filed Critical Syngenta Participations Ag
Priority to US11/570,980 priority Critical patent/US20080318962A1/en
Priority to BRPI0512558-8A priority patent/BRPI0512558A/en
Priority to JP2007517181A priority patent/JP2008503527A/en
Priority to EP05753230A priority patent/EP1771423A1/en
Publication of WO2005123698A1 publication Critical patent/WO2005123698A1/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system

Abstract

The compound of the general formula (I), wherein W, X, Y, Z, R, R1 and R2 are defined as set forth in the specification, useful as fungicide.

Description

FUNGICIDES BASED ON NITROGEN-CONTAINING HETEROCYCLES
This invention relates to novel pyridine derivatives having a condensed, nitrogen- containing heterocyclic ring, to processes for preparing them, to certain intermediate chemicals used in their manufacture, to compositions containing them and to methods of using them to combat fungi, especially fungal infections of plants. Derivatives of the nitrogen-containing 5,6 ring system ,s-l,2,4-triazolo[l,5-a]pyri- midine are known from the patent literature as being useful for controlling phytopathogenic fungi. Examples of recent patent publications include EP-A-1249452, WO 02/051845, WO 02/083676, WO 02/083677, WO 02/088125, WO 02/088126, WO 02/088127. Derivatives of pyridopyrazines are known in the chemical literature, for example from J. Med. Chem. (1968), 11(6), 1216-18, 7. Med. Chem. (1970), 13(5), 853-7 and US 3984412, but not for agrochemical purposes. The present invention is concerned with the provision of novel pyridine derivatives having a condensed, nitrogen-containing heterocyclic ring for combating phytopathogenic diseases on plants and harvested food crops. Thus, according to the present invention, there is provided a compound of the general formula (1):
Figure imgf000002_0001
wherein
W, X, Y and Z can be N or CR8, with at least one and no more than three of W, X, Y and Z being N, but excluding compounds where W, X, Y = N and Z = CR8, and X, Y, Z = N and Z
= CR8;
R8 is H, halo, C1-4 alkyl, C1- alkoxy or halo(C1-4)alkyl, CN, C1-4alkylthio, C1-4alkylsulphinyl, C1. alkylsulphonyl, aryl, heteroaryl, halo(Cι-6)alkoxy, halo(Cι- )alkylthio, C2-4alkenyl, C24-
6alkynyl, C2-6cycloalkyl, or NR3R4 ;
R is H, C1-4 alkyl, halo(C1-4)alkyl, cyano, halogen or NR3R4;
R2 is halo or NR3R4;
R1 is an aryl or heteroaryl ring R20, of the general formula
Figure imgf000003_0001
where A can be one to four optional substituents independently selected from halo, C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, C1-6 alkoxy, C2-6 alkenyloxy, C2-6 alkynyloxy, halo(Cι. e)alkyl, halo(C1-6)alkoxy, -6 alkylthio, halo(C1-6)alkylthio, C1- alkoxy(C1-6)alkyl, C3.6 cycloalkyl, C3-6 cycloalkyl(C1- )alkyl, and B is at least one or more substituents independently selected from aryl, heteroaryl, aryloxy (except that phenoxy must be substituted), heteroaryloxy, aryl(C]-4)alkoxy (except that benzyloxy must be substituted), heteroaryl(C1-4)alkoxy, arylthio, arylsulphinyl, arylsulphonyl, heteroarylthio, heteroarylsulphinyl, heteroarylsulphonyl, aryl(C -4)alkenyl, aryl(C2-4)alkynyl, heteroaryl(C2- )alkenyl, heteroaryl(C2-4)alkynyl, aryl(C1- )alkyl, heteroaryl(C1-4)alkyl, with any of the forgoing aryl or heteroaryl substituents being optionally substituted with halo, C1-6 alkyl, C -6 alkenyl, C2-6 alkynyl, C1-6 alkoxy, C -6 alkenyloxy, C2-6 alkynyloxy, halo(C1-6)alkyl, halo(C1-6)alkoxy, C1-6 alkylthio, halo(C1-6)- alkylthio, C1-4 alkoxy(C1-6)alkyl, C3-6 cycloalkyl, cyano or nitro;
R3 and R4 are independently H, C1-8 alkyl, C -8 alkenyl, C -8 alkynyl, aryl, aryl(C1- )alkyl, C3-8 cycloalkyl, C3-8 cycloalkyl(C1-6)alkyl, heteroaryl, heteroaryl(C1-8)alkyl, NR5R6, usually under the provision that not both R3 and R4 are H or NR5R6, or R3 and R4 together form a C3-7 alkylene or C3-7 alkenylene chain optionally substituted with one or more C1-4 alkyl or C1-4 alkoxy groups, or, together with the nitrogen atom to which they are attached, R3 and R4 form a morpholine, thiomorpholine, thiomorpholine S-oxide or thiomorpholine S-dioxide ring or a piperazine or piperazine N-(C1-4)alkyl (especially N-methyl) ring; and R5 and R6 are independently H, C1-8 alkyl, C2-8 alkenyl, C2-8 alkynyl, aryl, aryl(C1-8)alkyl, C3-8 cycloalkyl, C3-8 cycloalkyl(C1-6)alkyl, heteroaryl or heteroaryl(C1-8)alkyl; any of the foregoing alkyl, alkenyl, alkynyl or cycloalkyl groups or moieties (other than for R8) being optionally substituted with halogen, cyano, C1-6 alkoxy, C1-6 alkylcarbonyl, C1-6 alkoxycarbonyl, C1-6 haloalkoxy, C1-6 alkylthio, tri(C1-4)alkylsilyl, Cj-6 alkylamino or C1-6 dialkylamino, any of the foregoing morpholine, thiomorpholine, piperidine, piperazine and pyrrolidine rings being optionally substituted with C1-4 alkyl (especially methyl), and any of the foregoing aryl or heteroaryl groups or moieties in R3, R4, R5, R6 or R8 being optionally substituted with one or more substituents selected from halo, hydroxy, mercapto, C1-6 alkyl, C -6 alkenyl, C -6 alkynyl, C1-6 alkoxy, C -6 alkenyloxy, C -6 alkynyloxy, halo(C1- 6)alkyl, halo(Cι-6)alkoxy, C1-6 alkylthio, halo(C1-6)alkylthio, hydroxy(C1-6)alkyl, C1- alkoxy(C1-6)alkyl, C3-6 cycloalkyl, C3-6 cycloalkyl(C1-4)alkyl, phenoxy, benzyloxy, benzoyloxy, cyano, isocyano, thiocyanato, isothiocyanato, nitro, -NR13R14, -NHCOR13, - NHCON R13R14, -CON R13R14, -SO2R13, -OSO2 R13, -CO R13, -C R13=N R14 or -N=CR13R14, in which R13 and R14 are independently hydrogen, Cι-4 alkyl, halo(C1- )alkyl, C1- alkoxy, halo(C1-4)alkoxy, Cj-4 alkylthio, C -6 cycloalkyl, C3-6 cycloalkyl(C1-4)alkyl, phenyl or benzyl, the phenyl and benzyl groups being optionally substituted with halogen, C1-4 alkyl or C1-4 alkoxy. The invention includes compounds of the general formula (1) as defined immediately above, preferably compounds in which: C alkylene and C3-7 alkenylene are excluded as chains formed by R3 and R4; preferably the C -6 chain that R3 and R4 may form may only be optionally substituted with one or more methyl groups; preferably thiomorpholine, thiomorpholine S-oxide, thiomorpholine S-dioxide and piperazine are excluded as rings that R3 and R4 may form; preferably tri(C1-4)alkylsilyl is excluded as a substituent of any alkyl, alkenyl, alkynyl or cycloalkyl group or moiety and any morpholine, piperidine or pyrrolidine ring is unsubstituted.
The compounds of the invention may contain one or more asymmetric carbon atoms and may exist as enantiomers (or as pairs of diastereoisomers) or as mixtures of such. They may also exist as diastereoisomers by virtue of restricted rotation about a bond. However, mixtures of enantiomers or diastereoisomers may be separated into individual isomers or isomer pairs, and this invention embraces such isomers and mixtures thereof in all proportions. It is to be expected that for any given compound, one isomer may be more fungicidally active than another. Except where otherwise stated, alkyl groups and alkyl moieties of alkoxy, alkylthio, etc., contain from 1 to 8, suitably from 1 to 6 and typically from 1 to 4, carbon atoms in the form of straight or branched chains. Examples are methyl, ethyl, n- and iso-oτopyl, n-, sec-, iso- and tert-butyl, rc-pentyl and zz-hexyl. Cycloalkyl groups contain from 3 to 8, typically from 3 to 6, carbon atoms and include bicycloalkyl groups such as the bicyclo[2.2.1]heptyl group. Haloalkyl groups or moieties are typically trichloromethyl or trifluoromethyl or contain a trichloromethyl or trifluoromethyl terminal group. The term fluoroalkyl is an alkyl group substituted by one or more fluorine atoms, as for example trifluoromethyl, difluoroethyl or an alkyl comprising a trifluoromethyl terminal group. Except where otherwise stated, alkenyl and alkynyl moieties also contain from 2 to 8, suitably from 2 to 6 and typically from 2 to 4, carbon atoms in the form of straight or branched chains. Examples are allyl, 2-methylallyl and propargyl. Optional substituents include halo, typically fluoro. An example of halo-substituted alkenyl is 3,4,4-trifluoro-«- butenyl. Halo includes fluoro, chloro, bromo and iodo. Most commonly it is fluoro, chloro or bromo and usually fluoro or chloro. Aryl is usually phenyl but also includes naphthyl, anthryl and phenanthryl. Heteroaryl is typically a 5- or 6-membered aromatic ring containing one or more O, N or S heteroatoms, which may be fused to one or more other aromatic or heteroaromatic rings, such as a benzene ring. Examples are thienyl, furyl, pyrrolyl, isoxazolyl, oxazolyl, oxadiazolyl, pyrazolyl, imidazolyl, triazolyl, isothiazolyl, tetrazolyl, thiadiazolyl, pyridyl, pyrimidinyl, pyrazinyl, pyridazinyl, triazinyl, benzofuryl, benzothienyl, dibenzofuryl, benzothiazolyl, benzoxazolyl, benzimidazolyl, indolyl, quinolinyl and quinoxalinyl groups and, where appropriate, N-oxides thereof. The 6,6-ring systems embraced by the general formula (1) are 1,8-naphthyri dines (where W, X and Y are all CR8 and Z is N), 1 ,7-naphthyridines (where W, X and Z are all CR8 and Y is N), 1,6-naphthyridines (where W, Y and Z are all CR8 and X is N), 1,5-naph- thyridines (where X, Y and Z are all CR8 and W is N), pyrido[2,3-c]pyridazines (where W and X are both CR8 and Y and Z are both N), pyrido[2,3-d]pyridazines (where W and Z are both CR8 and X and Y are both N), pyrido[3,2-c]pyridazines (where Y and Z are both CR8 and W and X are both N), pyrido[2,3-b]pyrazines (where X and Y are both CR8 and W and Z are both N), pyrido[2,3-d]pyrimidines (where W and Y are both CR8 and X and Z are both N), pyrido[3,2-d]pyrimidines (where X and Z are both CR8 and W and Y are both N), ρyrido[2,3-e][l,2,4Jtriazines (where Y is CR8 and W, X and Z are all N), and pyrido[3,2-e]- [l,2,4]triazines (where X is CR8 and W, Y and Z are all N). Of particular interest are pyrido[2,3-b]pyrazines and pyrido[3,2-e][l,2,4]triazines. R , which may be the same or different for the CR values of W, X, Y and Z, is H, halo (for example chloro or bromo), C1-4 alkyl (for example methyl), C1-4 alkoxy (for example methoxy) or halo(Cι- )alkyl (for example trifluoromethyl), CN, Cj.4alkylthio, Cι_ 4alkylsulphinyl, C1- alkylsulphonyl, aryl, heteroaryl, halo(C1-6)alkoxy, halo(C1- )alkylthio, C2-4alkenyl, C24-6alkynyl, C2-6cycloalkyl, or NR3R4. Usually R8 will be H. One of R and R2, preferably R2, is NR3R4. The other is typically halo, especially chloro or fluoro. In the case of pyrido[2,3-b]pyrazine ring systems, the more active compounds are those where R2 is NR3R4 and R is chloro or fluoro. R3 is typically Cι_8 alkyl (for example ethyl, n-propyl, n-butyl, sec-butyl (the S- or R-isomer or the racemate), isobutyl and tert-butyl), halo(C1-8)alkyl (for example 2,2,2-trifluoroethyl, 2,2,2-trifluoro-l- methylethyl (the S- or R-isomer or the racemate), 2,2,2-trifluoro-l-methylpropyl (the S- or R-isomer or the racemate), 3,3,3-trifluoropropyl and 4,4,4-trifluorobutyl), C1- alkoxy(Cμ 8)alkyl (for example methoxymethyl and methoxy- wø-butyl), C1-4 alkoxyhalo(C1.8)alkyl (for example 2-methoxy-2-trifluromethylethyl), C1-4 alkylcarbonyl(C1-8)alkyl (for example 1- acetylethyl and 1-tert-butylcarbonyl ethyl), C1- alkylcarbonylhalo(C1-8)alkyl (for example 1- acetyl-2,2,2-trifluoroethyl), phenyl(1-4)alkyl (for example benzyl), C -8 alkenyl (for example allyl and methylallyl), halo(C2-8)alkenyl (for example 3-methyl-4,4-difluorobut-3-enyl), C -8 alkynyl (for example propargyl), C3-8 cycloalkyl (for example cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl) optionally substituted with chloro, fluoro or methyl, C -8 cyclo- alkyl (C1- )alkyl (for example cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyl and cyclohexylmethyl), phenylamino, piperidino or morpholino, the phenyl ring of phenylalkyl or phenylamino being optionally substituted with one, two or three substituents selected from halo (typically fluoro, chloro or bromo), C1- alkyl (typically methyl), halo(C1- )alkyl (typically trifluoromethyl), C1- alkoxy (typically methoxy) and halo(C1- )alkoxy (typically trifluoromethoxy). R4 is typically H, C1- alkyl (for example ethyl and n-propyl), halo(C1-4)- alkyl (for example 2,2,2-trifluoroethyl) or amino. Alternatively R3 and R4 together form a C4-6 alkylene chain optionally substituted with methyl, for example 3-methylpentylene, or, together with the nitrogen atom to which they are attached, R3 and R4 form a morpholine, thiomorpholine, thiomorpholine S-oxide or thiomorpholine S-dioxide ring or a piperazine or piperazine N-(C1- )alkyl (especially N-methyl) ring, in which the morpholine or piperazine rings are optionally substituted with methyl.
Typically R1 is an aromatic carbocyclic or heterocyclic ring of formula R20, preferably -an optionally substituted phenyl, pyridyl or thiazole group, and A is from one to four independent halogen atoms, particularly fluorine and chlorine atoms and especially fluorine atoms, or is from one to three substituents selected from halo (for example fluoro and chloro), C1- alkyl (for example methyl), halo(C1- )alkyl (for example trifluoromethyl), C1- alkoxy (for example methoxy) or halo(C1-4)alkoxy (for example trifluoromethoxy), and B is at least one or more of the substituents selected from the group comprising aryl, heteroaryl, aryloxy (except that phenoxy must be substituted), heteroaryloxy, aryl(C1.4)alkoxy (except that benzyloxy must be substituted), heteroaryl(C1- )alkoxy, arylthio, arylsulphinyl, arylsulphonyl, heteroarylthio, heteroarylsulphinyl, heteroarylsulphonyl, aryl(C -4)alkenyl, aryl(C2-4)alkynyl, heteroaryl(C2-4)alkenyl, heteroaryl(C2-4)alkynyl, aryl(C1- )alkyl, heteroaryl (C1-4)alkyl. Examples are 2,6-difluoro-4-phenyl-phenyl, 2-fluoro-4-phenyl-6- chlorophenyl, 2,5,6-trifluoro-4-phenyl phenyl, 2,4,6-trifluoro-4-phenyl-phenyl, 2-chloro-4- phenyl-phenyl, 2-fluoro-4-phenyl-6-methoxyphenyl, and 2-fluoro-6-trifluoromethyl-4- phenyl-phenyl. Also of particular interest are compounds where R1 is an aryl or heteroaryl ring R20 being a pyridyl group and A is from one to three halogen atoms or with from one to three substituents selected from halo (for example fluoro and chloro), C1-4 alkyl (for example methyl), halo(C1-4)alkyl (for example trifluoromethyl), C1-4 alkoxy (for example methoxy) or halo(C1-4)alkoxy (for example trifluoromethoxy) and B is at least one or more substituents selected from aryl, heteroaryl, aryloxy (except that phenoxy must be substituted), heteroaryloxy, aryl(C1-4)alkoxy (except that benzyloxy must be substituted), heteroaryl(Cι. 4)alkoxy, arylthio, arylsulphinyl, arylsulphonyl, heteroarylthio, heteroarylsulphinyl, heteroarylsulphonyl, aryl(C -4)alkenyl, aryl(C -4)alkynyl, heteroaryl(C - )alkenyl, heteroaryl (C2-4)alkynyl, aryl(C1-4)alkyl, heteroaryl(C1- )alkyl. Examples are 3-fluoro-5- phenylpyrid-2-yl, 3-chloro-5-phenylpyrid-2-yl and 3,5-difluoro-4-phenylpyrid-2-yl. In one aspect the invention provides a compound of the general formula (1) wherein
W and Z are N and the other two are CR8, or W, Y and Z are N and X is CR8, or W, X and Z are N and Y is CR8;
R8 is H, halo, C1- alkyl, C1- alkoxy or halo(C1-4)alkyl; one of R and R2 (preferably R2) is NR3R4 and the other is halo; R1 is an aryl or heteroaryl ring R20, and A is a substituent selected from halo, C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, C1-6 alkoxy, C -6 alkenyloxy, C2-6 alkynyloxy, halo(C1-6)alkyl, halo(C1- 6)alkoxy, C1-6 alkylthio, halo(C1-6)alkylthio, C1- alkoxy(C1-6)alkyl, C3-6 cycloalkyl, C3-6 cycloalkyl(C1-4)alkyl, and B is at least one or more substituents selected from aryl, heteroaryl, aryloxy (except that phenoxy must be substituted), heteroaryloxy, aryl(Ci. )alkoxy (except that benzyloxy must be substituted), heteroaryl(C1-4)alkoxy, arylthio, arylsulphinyl, arylsulphonyl, heteroarylthio, heteroarylsulphinyl, heteroarylsulphonyl, aryl(C2- )alkenyl, aryl(C2- )alkynyl, heteroaryl(C2- )alkenyl, heteroaryl(C2- )alkynyl, ary Ci. )alkyl, heteroaryl(C1-4)alkyl, with any of the forgoing aryl or heteroaryl substituents being optionally substituted with halo, C1-6 alkyl, C2-6 alkenyl, C -6 alkynyl, C1-6 alkoxy, C -6 alkenyloxy, C -6 alkynyloxy, halo(C1-6)alkyl, halo(C1-6)alkoxy, C1-6 alkylthio, halo(C1-6)- alkylthio, C1-4 alkoxy(C1-6)alkyl, C3-6 cycloalkyl, cyano or nitro; R3 and R4 are independently H, C1-8 alkyl, C -8 alkenyl, C2-8 alkynyl, aryl, aryl(C1-8)alkyl, C3-8 cycloalkyl, C3-8 cycloalkyl(C1-6)alkyl, heteroaryl, heteroaryl(C1_8)alkyl, NR5R6, provided that at least one of R3 and R4 is NR5R6, or
R3 and R4 together form a C3-7 alkylene or C3-7 alkenylene chain optionally substituted with one or more C1-4 alkyl or C1-4 alkoxy groups, or, together with the nitrogen atom to which they are attached, R3 and R4 form a morpholine, thiomorpholine, thiomoφholine S-oxide or thiomoφholine S-dioxide ring or a piperazine or piperazine N-(C1-4)alkyl (especially N-methyl) ring; and
R and R are independently H, C1-8 alkyl, C -8 alkenyl, C2-8 alkynyl, aryl, aryl(C1-8)alkyl, C3-8 cycloalkyl, C3-8 cycloalkyl (C1-6)alkyl, heteroaryl or heteroaryl (C1-8)alkyl; any of the foregoing alkyl, alkenyl, alkynyl or cycloalkyl groups or moieties (other than for R8) being optionally substituted with halogen, cyano, C1-6 alkoxy, Cι-6 alkylcarbonyl, C1-6 alkoxycarbonyl, C1-6 haloalkoxy, C1-6 alkylthio,
Figure imgf000008_0001
C1-6 alkylamino or C1-6 dialkylamino, any of the foregoing moφholine, thiomoφholine, piperidine, piperazine and pyrrolidine rings being optionally substituted with C1-4 alkyl (especially methyl). Of particular interest are compounds where W and Z are both Ν and X and Y are both CH. In a further embodiment, the invention includes a compound of the general formula
(1) as defined immediately above except that: C7 alkylene and C3-7 alkenylene are excluded as chains formed by R3 and R4; the C3-6 chain that R3 and R4 may form may only be optionally substituted with one or more methyl groups; thiomoφholine, thiomoφholine S- oxide, thiomoφholine S-dioxide and piperazine are excluded as rings that R3 and R4 may form; tri(C1- )alkylsilyl is excluded as a substituent of any alkyl, alkenyl, alkynyl or cycloalkyl group or moiety, and any moφholine, piperidine or pyrrolidine ring is unsubstituted. In yet a further embodiment of the present invention, the compound of formula 1 the values of the substituents are defined as follows:
R3 is Cι-8 alkyl, halo(C1-8)alkyl, haloC1-4 alkoxy (Cι.8)alkyl, C1-4 alkoxyhalo(C1-8)alkyl, C1.4alkoxycarbonyl(C1-8)alkyl, C1- alkoxycarbonylhalo(C1-8)alkyl, phenyl(1- )alkyl, C2-8 alkenyl, halo(C -8)alkenyl, C2-8 alkynyl, C3-8 cycloalkyl optionally substituted with chloro, fluoro or methyl, C -8 cycloalkyl(C1- )alkyl, phenylamino, piperidino or moφholino, the phenyl ring of phenylalkyl or phenylamino being optionally substituted with one, two or three substituents selected from halo, C1- alkyl, halo(C1-4)alkyl, C1-4 alkoxy and halo- (C1-4)alkoxy; and R4 is H, C1- alkyl, halo(C1-4)alkyl or amino, or R3 and R4 together form a C - alkylene or alkenylene chain optionally substituted with methyl, or, together with the nitrogen atom to which they are attached, R3 and R4 form a moφholine, thiomoφholine, thiomoφholine S-oxide or thiomoφholine S-dioxide ring or a piperazine or piperazine N- (C1- )alkyl (especially N-methyl) ring, in which the moφholine or piperazine rings are optionally substituted with methyl. Of particular interest are compounds in which R is halo, and/or R2 is ΝR3R4, where NR3R4 are as defined above, and/or W and Z are N and X and Y are CH. A further embodiment of the invention provides a compound of formula (1) wherein W, X and Z are N and Y is CR8; R8 is H or halo; R is halo and R2 is NR3R4; R1 is an aryl or heteroaryl ring R20 and A is a substituent selected from halo, C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, and B is one more substituent selected from aryl, heteroaryl, aryloxy (except that phenoxy must be substituted), heteroaryloxy, arylthio, arylsulphinyl, arylsulphonyl, heteroarylthio, heteroarylsulphinyl, heteroarylsulphonyl, aryl(C2-4)alkenyl, aryl(C2-4)alkynyl, heteroaryl(C .4)alkenyl, heteroaryl(C -4)alkynyl, aryl(C1-4)alkyl, heteroaryl(C1-4)alkyl, with any of the forgoing aryl or heteroaryl substituents being optionally substituted with halo, C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, C1-6 alkoxy, cyano or nitro; R3 and R4 are independently H, C1-8 alkyl, C1-8 fluoroalkyl, C1-8 perfluoroalkyl C2-8 alkenyl, C2-8 alkynyl, aryl, C3-8 cycloalkyl, heteroaryl. Of particular interest are compounds of the general formula (1) as defined immediately above except that: C alkylene and C3- alkenylene are excluded as chains formed by R3 and R4; tri(C1-4)alkylsilyl is excluded as a substituent of any alkyl, alkenyl, alkynyl or cycloalkyl group or moiety, and any moφholine, piperidine or pyrrolidine ring is unsubstituted. In a further embodiment of the invention as defined immediately above, the compounds of formula (1) are compounds in which W, X and Z are N, and the respective other ring members are CH; R is chloro or fluoro; R2 is NR3R4;
R1 is an aryl or heteroaryl ring of formula R20;
R20 is 4-substituted 2,6-difluorophenyl, 4-substituted 2,3,6-trifluorophenyl, 3-substituted 2,4,6-trifluorophenyl, 4-substituted 2-chloro-6-fluorophenyl, 4-substituted 2-chlorophenyl, 5- substituted 3-fluoropyrid-2-yl, 5-substituted 3-chloropyrid-2-yl, 2-substituted 4-chloro- thiazol-5-yl, 2-substituted 4-fluoro-thiazol-5-yl;
R3 is hydrogen, methyl, ethyl, 1,1,1-trifiuoroethyl, 2-methylpropen-3-yl; R4 is prop-2-yl, but-2-yl, 2-methylprop-3-yl, 2-methylbut-3-yl, l,l,l-trifluoroprop-2-yl, 1,1,1-trifluoroethyl, 1,1,1 -trifluorobut-2-yl, l,l,l-trifluoro-3-methyl-but-2-yl; 2-methylpent- 4-yl, l,l,l-trifluoro-4-methylpent-2-yl, l,l,l-trifluoro-3-methylpent-2-yl, 3-methylpent-2-yl, l,l,-difluorocyclopent-2-yl, heptafluoroprop-1-yl, nonafluorobut-1-yl, 1-carboxyethyl-
2.methylprop- 1 -yl, 1 -carboxymethyl-2-methylprop- 1 -yl, 1,1,1 ,-trifluoro-2-carboxyethyl-2- ethyl, l,l,l,-trifluoro-2-carboxymethyl 2-ethyl;
B is phenyl, 4-fluorophenyl, 2-fluorophenyl, 3-fluorophenyl, 4-chlorophenyl, 2-chlorophenyl, 3-chlorophenyl, 2-pyridyl, 3-pyridyl, 4-pyridyl, 5-fluoro-2 -pyridyl, 6-fluoro-3-pyridyl, 2-fluoro-4-pyridyl, 2-phenylethenyl, 2-(4-fluorophenyl)ethenyl, phenyl ethynyl, (4-methylphenyl)ethynyl, (4-fluorophenyl)ethynyl, 4-fluorophenoxy, 2-fluorophenoxy, 3-fluorophenoxy, phenylthio, phenylsulphinyl, phenylsulphonyl; or, in another embodiment of the invention, W, X and Z are N, and the respective other ring members are CH; R is chloro or fluoro; R2 is NR3R4;
R1 is an aryl or heteroaryl ring of formula R20;
R20 is 4-substituted 2,6-difluorophenyl, 4-substituted 2-chloro-6-fluorophenyl, 4-substituted 2-chlorophenyl, 5-substituted 3-fluoropyrid-2-yl, 5-substituted 3-chloropyrid-2-yl; R3 is hydrogen, ethyl, 2-methylpropen-3-yl;
R4 is prop-2-yl, but-2-yl, 2-methylprop-3-yl, 2-methylbut-3-yl, l,l,l-trifluoroprop-2-yl, 1,1,1-trifluoroethyl, l,l,l-trifluorobut-2-yl, l,l,l-trifluoro-3-methyl-but-2-yl; 1,1,1-trifluoro- 4-methylpent-2-yl, 1,1,1 -trifluoro-3-methylpent-2-yl, 1 , 1 ,-difluorocyclopent-2-yl, heptafluoroprop- 1 -yl, 1 -carboxyethyl-2-methylprop- 1 -yl, 1,1,1 ,-trifluoro-2-carboxyethyl-2- ethyl; B is phenyl, 4-fiuorophenyl, 4-chlorophenyl, 5-fluoro-2-pyridyl, 6-fluoro-3-pyridyl, 2-phenylethenyl, 2-(4-fluorophenyl)ethenyl, (4-methylphenyl)ethynyl, (4-fluorophenyl) ethynyl, 4-fluorophenoxy, phenylthio, phenylsulphinyl (or benzensulphinyl), phenylsulphonyl (or benzenesulphonyl).
Yet another aspect of the invention provides a compound of formula (1) wherein wherein W and Z are N and the other two are CR8, or W, Y and Z are N and X is CR8, R8 is H or halo; R is halo and R2 is NR3R4; R1 is an aryl or heteroaryl ring R20 and A is a substituent selected from halo, Cj-6 alkyl, C2-6 alkenyl, C -6 alkynyl, and B is one more substituent selected from aryl, heteroaryl, aryloxy (except that phenoxy must be substituted), heteroaryloxy, arylthio, arylsulphinyl, arylsulphonyl, heteroarylthio, heteroarylsulphinyl, heteroarylsulphonyl, aryl(C2-4)alkenyl, aryl(C2-4)alkynyl, heteroaryl(C2-4)alkenyl, heteroaryl(C2-4)alkynyl, aryl(C1- )alkyl, heteroaryl (C1-4)alkyl, with any of the forgoing aryl or heteroaryl substituents being optionally substituted with halo, C1-6 alkyl, C2-6 alkenyl, C -6 alkynyl, C1-6 alkoxy, cyano or nitro; R3 and R4 are independently H, C1-8 alkyl, Cι-8 fluoroalkyl, C1-8 perfluoroalkyl, C2-8 alkenyl, C2-8 alkynyl, aryl, C3-8 cycloalkyl, heteroaryl.
In a further embodiment, the invention includes a compound of the general formula (1) as defined immediately above except that: C7 alkylene and C3- alkenylene are excluded as chains formed by R3 and R4; tri(C1-4)alkylsilyl is excluded as a substituent of any alkyl, alkenyl, alkynyl or cycloalkyl group or moiety, and any moφholine, piperidine or pyrrolidine ring is unsubstituted.
In a further embodiment of the invention, in the compounds of formula (1) are compounds in which W and Z are N, or W, Y and Z are N, and the respective other ring members are CH; R is chloro or fluoro; R2 is NR3R4;
R1 is an aryl or heteroaryl ring of formula R20;
R20 is 4-substituted 2,6-difluorophenyl, 4-substituted 2,3,6-trifluorophenyl, 3-substituted
2,4,6-trifluorophenyl, 4-substituted 2-chloro-6-fluorophenyl, 4-substituted 2-chlorophenyl, 5- substituted 3-fluoropyrid-2-yl, 5-substituted 3-chloropyrid-2-yl, 2-substituted 4-chloro- thiazol-5-yl, 2-substituted 4-fluoro-thiazol-5-yl;
R3 is hydrogen, methyl, ethyl, 1,1,1-trifluoroethyl, 2-methylpropen-3-yl;
R4 is prop-2-yl, but-2-yl, 2-methylprop-3-yl, 2-methylbut-3-yl, l,l,l-trifluoroprop-2-yl, 1,1,1-trifluoroethyl, l,l,l-trifluorobut-2-yl, l,l,l-trifluoro-3-methyl-but-2-yl; 2-methylpent-
4-yl, l,l,l-trifluoro-4-methylpent-2-yl, l,l,l-trifluoro-3-methylpent-2-yl, 3-methylpent-2-yl, l,l,-difluorocyclopent-2-yl, heptafluoroprop-1-yl, nonafluorobut-1-yl, 1-carboxyethyl-
2.methylprop- 1 -yl, 1 -carboxymethyl-2-methylprop- 1 -yl , 1,1,1 ,-trifluoro-2-carboxyethyl-2- ethyl, l,l,l,-trifluoro-2-carboxymethyl 2-ethyl; B is phenyl, 4-fluorophenyl, 2-fluorophenyl, 3-fluorophenyl, 4-chlorophenyl,
2-chlorophenyl, 3-chlorophenyl, 2-pyridyl, 3-pyridyl, 4-pyridyl, 5-fluoro-2 -pyridyl,
6-fluoro-3-pyridyl, 2-fluoro-4-pyridyl, 2-phenylethenyl, 2-(4-fluorophenyl)ethenyl, phenylethynyl, (4-methylphenyl)ethynyl, (4-fluorophenyl)ethynyl, 4-fluorophenoxy,
2-fluorophenoxy, 3-fluorophenoxy, phenylthio, phenylsulphinyl, phenylsulphonyl, or benzenesulponyl ; or, in another embodiment of the invention,
W and Z are N, or W, Y and Z are N, and the respective other ring members are CH;
R is chloro or fluoro;
R2 is NR3R4; R1 is an aryl or heteroaryl ring of formula R20;
R20 is 4-substituted 2,6-difluorophenyl, 4-substituted 2-chloro-6-fluorophenyl, 4-substituted
2-chlorophenyl, 5-substituted 3-fluoropyrid-2-yl, 5-substituted 3-chloropyrid-2-yl;
R3 is hydrogen, ethyl, 2-methylpropen-3-yl;
R4 is prop-2-yl, but-2-yl, 2-methylprop-3-yl, 2-methylbut-3-yl, l,l,l-trifluoroprop-2-yl, 1,1,1-trifluoroethyl, l,l,l-trifluorobut-2-yl, l,l,l-trifluoro-3-methyl-but-2-yl; 1,1,1-trifluoro-
4-methylpent-2-yl, 1,1,1 -trifluoro-3-methylpent-2-yl, 1 , 1 ,-difluorocyclopent-2-yl, heptafluoroprop- 1 -yl, 1 -carboxyethyl-2-methylprop- 1 -yl, 1,1,1 ,-trifluoro-2-carboxyethyl-2- ethyl;
B is phenyl, 4-fluorophenyl, 4-chlorophenyl, 5-fluoro-2-pyridyl, 6-fluoro-3-pyridyl, 2- phenylethenyl, 2-(4-fluorophenyl)ethenyl, (4-methylphenyl)ethynyl, (4-fluorophenyl) ethynyl, 4-fluorophenoxy, phenylthio, phenylsulphinyl (or benzensulphinyl), phenylsulphonyl (or benzenesulphonyl). Compounds that form part of the invention are illustrated in Tables 1 to 27 below. Characterising data are given later in the Examples. Single compounds are assigned the number of the table, followed by the number of the combination of substituents as in Table 1. For example, compound 22.005 is the compound as described in Table 22, wherein the substituents defined therein are combined with the substituents as defined in Table 1, position No. 5. In Table 1 to 27 the compounds have the general formula (2) as depicted below.
Figure imgf000013_0001
Table 1
Figure imgf000013_0002
Figure imgf000014_0001
Figure imgf000015_0001
Figure imgf000016_0001
Figure imgf000017_0001
Figure imgf000018_0001
Figure imgf000019_0001
Figure imgf000020_0001
Figure imgf000021_0001
Figure imgf000022_0001
Figure imgf000023_0001
Figure imgf000024_0001
Figure imgf000025_0001
Figure imgf000026_0001
Figure imgf000027_0001
Figure imgf000028_0001
Figure imgf000029_0001
Figure imgf000030_0001
Figure imgf000031_0001
Figure imgf000032_0001
Figure imgf000033_0001
Figure imgf000034_0001
Figure imgf000035_0001
Figure imgf000036_0001
Figure imgf000037_0001
Figure imgf000038_0001
Figure imgf000039_0001
Figure imgf000040_0001
Figure imgf000041_0001
Figure imgf000042_0001
Figure imgf000043_0001
Figure imgf000044_0001
Figure imgf000045_0001
Figure imgf000046_0001
Figure imgf000047_0001
Figure imgf000048_0001
Figure imgf000049_0001
Figure imgf000050_0001
Figure imgf000051_0001
Figure imgf000052_0001
Figure imgf000053_0001
Figure imgf000054_0001
Table 2 Table 2 consists of 453 compounds of the general formula (2), where W and Z are N, X and Y are CH, B is phenyl, and the values of R, R3,R4 and R20 are as listed in Table 1.
Table 3 Table 3 consists of 453 compounds of the general formula (2), where W and Z are N, X and Y are CH, B is 4-fluorophenyl, and the values of R, R3,R4 and R20 are as listed in Table 1.
Table 4 Table 4 consists of 453 compounds of the general formula (2), where W and Z are N, X and Y are CH, B is 4-chlorophenyl, and the values of R, R3,R4 and R20 are as listed in Table 1.
Table 5 Table 5 consists of 453 compounds of the general formula (2), where W and Z are N, X and Y are CH, B is 5-fluoro-2-pyridyl, and the values of R, R3,R4 and R20 are as listed in Table 1. Table 6 Table 6 consists of 453 compounds of the general formula (2), where W and Z are N,
X and Y are CH, B is 6-fluoro-3-pyridyl, and the values of R, R3,R4 and R20 are as listed in
Table 1.
Table 7 Table 7 consists of 453 compounds of the general formula (2), where W and Z are N,
X and Y are CH, B is 2-phenylethenyl, and the values of R, R3,R4 and R20 are as listed in
Table 1.
Table 8 Table 8 consists of 453 compounds of the general formula (2), where W and Z are N,
X and Y are CH, B is 2-(4-fluorophenyl)ethenyl, and the values of R, R3,R4 and R20 are as listed in Table 1.
Table 9 Table 9 consists of 453 compounds of the general formula (2), where W and Z are N,
X and Y are CH, B is (4-methylphenyl)ethynyl, and the values of R, R3,R4 and R20 are as listed in Table 1.
Table 10 Table 10 consists of 453 compounds of the general formula (2), where W and Z are
N, X and Y are CH, B is (4-fluorophenyl)ethynyl, and the values of R, R3,R4 and R20 are as listed in Table 1.
Table 11 Table 11 consists of 453 compounds of the general formula (2), where W and Z are
N, X and Y are CH, B is 4-fluorophenoxy, and the values of R, R3,R4 and R20 are as listed in
Table 1.
Table 12 Table 12 consists of 453 compounds of the general formula (2), where W and Z are
N, X and Y are CH, B is phenylthio, and the values of R, R3,R4 and R20 are as listed in Table
1. Table 13 Table 13 consists of 453 compounds of the general formula (2), where W and Z are
N, X and Y are CH, B is phenylsulphinyl, and the values of R, R3,R4 and R20 are as listed in
Table 1.
Table 14 Table 14 consists of 453 compounds of the general formula (2), where W and Z are
N, X and Y are CH, B is phenylsulphonyl, and the values of R, R3,R4 and R20 are as listed in
Table 1.
Table 15 Table 15 consists of 453 compounds of the general formula (2), where W, Y and Z are N, X is CH, B is phenyl, and the values of R, R3,R4 and R20 are as listed in Table 1.
Table 16 Table 16 consists of 453 compounds of the general formula (2), where W, Y and Z are N, X is CH, B is 4-fluorophenyl, and the values of R, R3,R4 and R20 are as listed in Table 1.
Table 17 Table 17 consists of 453 compounds of the general formula (2), where W, Y and Z are N, X is CH, B is 4-chlorophenyl, and the values of R, R3,R4 and R20 are as listed in Table 1.
Table 18 Table 18 consists of 453 compounds of the general formula (2), where W, Y and Z are N, X is CH, B is 5-fluoro-2-pyridyl, and the values of R, R3,R4 and R20 are as listed in Table 1.
Table 19 Table 19 consists of 453 compounds of the general formula (2), where W, Y and Z are N, X is CH, B is 6-fluoro-3-pyridyl, and the values of R, R3,R4 and R20 are as listed in Table 1. Table 20 Table 20 consists of 453 compounds of the general formula (2), where W, Y and Z are N, X is CH, B is 2-phenylethenyl, and the values of R, R3,R4 and R20 are as listed in
Table 1.
Table 21 Table 21 consists of 453 compounds of the general formula (2), where W, Y and Z are N, X is CH, B is 2-(4-fluorophenyl)ethenyl, and the values of R, R3,R4 and R20 are as listed in Table 1.
Table 22 Table 22 consists of 453 compounds of the general formula (2), where W, Y and Z are N, X is CH, B is (4-methylphenyl)ethynyl, and the values of R, R3,R4 and R20 are as listed in Table 1.
Table 23 Table 23 consists of 453 compounds of the general formula (2), where W, Y and Z are N, X is CH, B is (4-fluorophenyl)ethynyl, and the values of R, R3,R4 and R20 are as listed in Table 1.
Table 24 Table 24 consists of 453 compounds of the general formula (2), where W, Y and Z are N, X is CH, B is 4-fluorophenoxy, and the values of R, R3,R4 and R20 are as listed in
Table 1.
Table 25 Table 25 consists of 453 compounds of the general formula (2), where W, Y and Z are N, X is CH, B is phenylthio, and the values of R, R3,R4 and R20 are as listed in Table 1.
Table 26 Table 26 consists of 453 compounds of the general formula (2), where W, Y and Z are N, X is CH, B is phenylsulphinyl, and the values of R, R3,R4 and R20 are as listed in
Table 1. Table 27 Table 27 consists of 453 compounds of the general formula (2), where W, Y and Z are N, X is CH, B is phenylsulphonyl, and the values of R, R3,R4 and R20 are as listed in
Table 1.
Compounds of formula (7) or (8), which are examples of compounds of general formula (1) where one of R and R is NR R , can be made as shown in Scheme 1, in which W, X, Y, Z, R1, R3 and R4 have the meanings given above and R7 is C1-4 alkyl.
Scheme 1
Figure imgf000058_0001
Compounds of general formula (4) can be prepared from compounds of general formula (2), which are either commercially available or made by methods known in the literature, by reaction with acids of general formula (3), using standard coupling methods, for example by conversion to the acid chloride using a chlorinating agent such as thionyl chloride, followed by reaction of the resultant acid chloride optionally in the presence of a base such as triethylamine, in a suitable solvent such as dichloromethane or toluene. Compounds of general formula (5) can be prepared by treating compounds of general formula (4) with a base such as sodium hydride, optionally in the presence of a Lewis acid such as magnesium oxide, in a suitable solvent such as NN-dimethylformamide (DMF) or toluene, at between room temperature and 150°C, but preferably at 60-90°C. Compounds of general formula (6) can be prepared by reaction of compounds of general formula (5) with a chlorination reagent such as phosphorus oxychloride, either neat or in a suitable solvent such as toluene, at between 50 and 150°C, but preferably between 80 and 110°C, or in a microwave reactor at between 150 and 300°C, but preferably between 200 and 250°C. Compounds of formula (7) and (8) can be prepared by reaction of compounds of general formula (6) with an amine R3R4ΝH, either neat, or in a suitable solvent such as DMF, between room temperature and 150°C, but preferably between 50 and 80°C. If compounds (7) and (8) are produced as a mixture they can be separated by suitable means such as crystallisation or chromatography under normal or reverse phase conditions. Compounds of formula (15) and (16), which are examples of compounds of general formula (1) can be made as shown in Scheme 2, where Hal is a halogen such as bromine or iodine. Compounds of formula (10), can be made by reaction of compounds of formula (9), which are examples of compounds of formula (5) in Scheme 1, by reaction with a compound B-D, where B is a substituent as defined above for R1, and D is a metallic group such as a boronic acid B(OH)2, or a tri(C1- ) alkyl tin, in a cross-coupling reaction in the presence of a palladium catalyst for example PdP(Ph3)4 or Pd2(dba)3, a ligand for example PPh3 or P(t-Bu)3, a base for example K2CO3 or CsF, in a suitable solvent such as toluene or ethanol, at room temperature to reflux, but preferably at between 50 and 100°C. Compounds of formula (11) can be formed by reaction of compounds of formula (9) with a chlorination reagent such as phosphorus oxychloride, either neat or in a suitable solvent such as toluene or dichlorethane, at between 50 and 150°C, but preferably between 60 and llO°C. Compounds of formula (12) can be made either by cross-coupling of compounds of formula (11) using conditions for converting (9) to (10), or by chlorination of compounds of formula (10) using conditions for converting (9) to (11). Compounds of formula (13) and (14) can be prepared by reacting compounds of formula (11) with an amine R3R4NH, either neat or in a suitable solvent such as DMF between room temperature, but preferably between 50 and 80°C. If compounds (13) and (14) are produced as a mixture they can be separated by suitable means such as crystallisation or chromatography under normal or reverse phase conditions. Compounds of formula (15) and (16) can be prepared by reacting compounds of formula (12) with an amine R3R4NH, either neat or in a suitable solvent such as DMF between room temperature, but preferably between 50 and 80°C. If compounds (15) and (16) are produced as a mixture they can be separated by suitable means such as crystallisation or chromatography under normal or reverse phase conditions. Compounds of formula (15) and (16) can also be prepared individually from compounds of formula (13) and (14) respectively by cross-coupling using conditions for converting (9) to (10).
Scheme 2
Figure imgf000061_0001
(11) (12)
R3RNH RWNH solvent solvent
Figure imgf000061_0002
Compounds of formula (17) can be prepared as shown in Scheme 3 from compounds of formula (6) by reaction with a source of fluoride ion, such as potassium fluoride, in a suitable solvent such as sulpholane, at a temperature between 50°C and 200°C, but preferably at 80- 150°C. Compounds of formula (18) and/or compounds of formula (19) can be prepared from difluoro compounds of formula (17) by reaction with an amine of formula R3R4NH in a suitable solvent such as DMF or CH C12, at a temperature of 0°C-100°C, but preferably at room temperature. Scheme 3
Figure imgf000062_0001
(17)
Figure imgf000062_0002
In Scheme 4 compounds of general formula (20), where the two R3R4N groups are identical, can be made from compounds of general formula (17) by reaction with a large excess of amine R3R4NH in a suitable solvent such as DMF, at a temperature between 0°C and 150°C, but preferably between room temperature and 100°C
Scheme 4
Figure imgf000062_0003
The intermediate chemicals having the general formulae (4), (5), (6), (9), (10), (11), (12), (13) (14) and (17) :
Figure imgf000063_0001
Figure imgf000063_0002
(9) (10) (11)
Figure imgf000063_0003
wherein W, X, Y, Z, R1, R3, R4, R7, Hal, A and B are as defined above, are believed to be novel compounds and form a further part of this invention. It should be noted that the intermediate of general formula (5) may exist in the tautomeric forms (a), (b) and (c) as well as in the form shown in formula (5):
Figure imgf000063_0004
(a) (b) (c) The invention as defined by the general formula (5) embraces all such tautomers. Of particular interest are the intermediates listed in Tables below. In Table 28, the compounds have the general formula (4) where R1 is R20, R7 is methyl, W, X, Y, Z and B have the values shown in table 28. Table 28
Figure imgf000064_0001
Table 29 Table 29 consists of 26 compounds of the general formula (5), where R1 is R20, W, X, Y, Z and B have the values given in Table 28 and R20 is 4-substituted 2,6-difluorophenyl.
Table 30 Table 30 consists of 26 compounds of the general formula (5), where R1 is R20, W, X, Y, Z and B have the values given in Table 28 and R20 is 4-substituted 2-chloro-6- fluorophenyl.
Table 31 Table 31 consists of 26 compounds of the general formula (5), where R1 is R20, W, X, Y, Z and B have the values given in Table 28 and R20 is 4-substituted 2-chlorophenyl.
Table 32 Table 32 consists of 26 compounds of the general formula (5), where R1 is R20, W, X,
Y, Z and B have the values given in Table 28 and R20 is 5-substituted 3-fluoropyrid-2-yl.
Table 33 Table 33 consists of 26 compounds of the general formula (5), where R1 is R20, W, X, Y, Z and B have the values given in Table 28 and R20 is 5-substituted 3-chloropyrid-2-yl.
Table 34 Table 34 consists of 26 compounds of the general formula (6), where R1 is R20, W, X,
Y, Z and B have the values given in Table 28 and R is 4-substituted 2,6-difluorophenyl.
Table 35 Table 35 consists of 26 compounds of the general formula (6), where R1 is R20, W, X, Y, Z and B have the values given in Table 28 and R20 is 4-substituted 2-chloro-6- fluorophenyl.
Table 36 Table 36 consists of 26 compounds of the general formula (6), where R1 is R20, W, X, Y, Z and B have the values given in Table 28 and R20 is 4-substituted 2-chlorophenyl. Table 37 Table 37 consists of 26 compounds of the general formula (6), where R1 is R20, W, X, Y, Z and B have the values given in Table 28 and R20 is 5-substituted 3-fluoropyrid-2-yl.
Table 38 Table 38 consists of 26 compounds of the general formula (6), where R1 is R20, W, X, Y, Z and B have the values given in Table 28 and R20 is 5-substituted 3-chloropyrid-2-yl.
Table 39 Table 39 consists of 26 compounds of the general formula (17), where R1 is R20, W,
X, Y, Z and B have the values given in Table 28 and R20 is 4-substituted 2,6-difluorophenyl.
Table 40 Table 40 consists of 26 compounds of the general formula (17), where R1 is R20, W, X, Y, Z and B have the values given in Table 28 and R20 is 4-substituted 2-chloro-6- fluorophenyl.
Table 41 Table 41 consists of 26 compounds of the general formula (17), where R1 is R20, W, X, Y, Z and B have the values given in Table 28 and R20 is 4-substituted 2-chlorophenyl.
Table 42 Table 42 consists of 26 compounds of the general formula (17), where R1 is R20, W, X, Y, Z and B have the values given in Table 28 and R20 is 5-substituted 3-fluoropyrid-2-yl.
Table 43 Table 43 consists of 26 compounds of the general formula (17), where R1 is R20, W, X, Y, Z and B have the values given in Table 28 and R20 is 5-substituted 3-chloropyrid-2-yl.
Table 44 Table 44 consists of 26 compounds of the general formula (4), where R1 is R20, W, X, Y, Z and B have the values given in Table 28, R7 is methyl and R20 is 4-substituted 2,6- difluorophenyl. Table 45 Table 45 consists of 26 compounds of the general formula (4), where R1 is R20, W, X, Y, Z and B have the values given in Table 28, R7 is methyl and R20 is 4-substituted 2-chloro- 6-fluorophenyl.
Table 46 Table 46 consists of 26 compounds of the general formula (4), where R1 is R20, W, X, Y, Z and B have the values given in Table 28, R7 is methyl and R20 is 4-substituted 2- chlorophenyl.
Table 47 Table 47 consists of 26 compounds of the general formula (4), where R1 is R20, W, X, Y, Z and B have the values given in Table 28, R7 is methyl and R20 is 5-substituted 3- fluoropyrid-2-yl.
Table 48 Table 48 consists of 26 compounds of the general formula (4), where R1 is R20, W, X, Y, Z and B have the values given in Table 28, R7 is methyl and R20 is 5-substituted 3- chloropyrid-2-yl.
Table 49 Table 49 consists of 26 compounds of the general formula (4), where R1 is R20, W, X, Y, Z and B have the values given in Table 28, R7 is ethyl and R20 is 4-substituted 2,6- difluorophenyl.
Table 50 Table 50 consists of 26 compounds of the general formula (4), where R1 is R20, W, X, Y, Z and B have the values given in Table 28, R7 is ethyl and R20 is 4-substituted 2-chloro-6- fluorophenyl. Table 51 Table 51 consists of 26 compounds of the general formula (4), where R1 is R20, W, X, Y, Z and B have the values given in Table 28, R7 is ethyl and R20 is 4-substituted 2- chlorophenyl.
Table 52 Table 52 consists of 26 compounds of the general formula (4), where R1 is R20, W, X, Y, Z and B have the values given in Table 28, R7 is ethyl and R20 is 5-substituted 3- fluoropyrid-2-yl.
Table 53 Table 53 consists of 26 compounds of the general formula (4), where R1 is R20, W, X, Y, Z and B have the values given in Table 28, R7 is ethyl and R20 is 5-substituted 3- chloropyrid-2-yl.
The compounds of formula (1) are active fungicides and may be used to control one or more of the following pathogens: Pyricularia oryz e (Magnaporthe grisea) on rice and wheat and other Pyricularia spp. on other hosts; Puccinia triticina (or recondita), Puccinia striiformis and other rusts on wheat, Puccinia hordei, Puccinia striiformis and other rusts on barley, and rusts on other hosts (for example turf, rye, coffee, pears, apples, peanuts, sugar beet, vegetables and ornamental plants); Erysiphe cichoracearum on cucurbits (for example melon); Blumeria (ox Erysiphe) graminis (powdery mildew) on barley, wheat, rye and turf and other powdery mildews on various hosts, such as Sphaerotheca macularis on hops, Sphaerothecafusca (Sphaerotheca fuliginea) on cucurbits (for example cucumber), Leveillula taurica on tomatoes, aubergine and green pepper, Podosphaera leucotricha on apples and Uncinula necator on vines; Cochliobolus spp., Helminthosporium spp., Drechslera spp. (Pyrenophora spp.), Rhynchosporium spp., Mycosphaerella graminicola (Septoria tritici) and Phaeosphaeria nodorum (Stagonospora nodorum or Septoria nodorum), Pseudocercosporella herpotrichoides and Gaeumannomyces graminis on cereals (for example wheat, barley, rye), turf and other hosts; Cercospora arachidicola and Cercosporidium personatum on peanuts and other Cercospora spp. on other hosts, for example sugar beet, bananas, soya beans and rice; Botrytis cinerea (grey mould) on tomatoes, strawberries, vegetables, vines and other hosts and other Botrytis spp. on other hosts; Alternaria spp. on vegetables (for example carrots), oil-seed rape, apples, tomatoes, potatoes, cereals (for example wheat) and other hosts; Venturia spp. (including Venturia inaequalis (scab)) on apples, pears, stone fruit, tree nuts and other hosts; Cladosporium spp. on a range of hosts including cereals (for example wheat) and tomatoes; Monilinia spp. on stone fruit, tree nuts and other hosts; Didymella spp. on tomatoes, turf, wheat, cucurbits and other hosts; Phoma spp. on oil-seed rape, turf, rice, potatoes, wheat and other hosts; Aspergillus spp. and Aureobasidium spp. on wheat, lumber and other hosts; Ascochyta spp. on peas, wheat, barley and other hosts; Stemphylium spp. (Pleospora spp.) on apples, pears, onions and other hosts; summer diseases (for example bitter rot (Glomerella cingulata), black rot or frogeye leaf spot (Botryosphaeria obtusa), Brooks fruit spot (Mycosphaerella pomi), Cedar apple rust (Gymnosporangiumjuniperi-virginianae), sooty blotch (Gloeodes pomigena), flyspeck (Schizothyrium pomi) and white rot (Botryosphaeria dothidea)) on apples and pears; Plasmopara viticola on vines;. other downy mildews, such as Bremia lactucae on lettuce, Peronospora spp. on soybeans, tobacco, onions and other hosts, Pseudoperonospora humuli on hops and Pseudoperonospora cubensis on cucurbits; Pythium spp. (including Pythium ultimum) on turf and other hosts; Phytophthora infestans on potatoes and tomatoes and other Phytophthora spp. on vegetables, strawberries, avocado, pepper, ornamentals, tobacco, cocoa and other hosts; Thanatephorus cucumeris on rice and turf and other Rhizoctonia spp. on various hosts such as wheat and barley, peanuts, vegetables, cotton and turf; Sclerotinia spp. on turf, peanuts, potatoes, oil-seed rape and other hosts; Sclerotium spp. on turf, peanuts and other hosts; Gibberellafujikuroi on rice; Colletotrichum spp. on a range of hosts including turf, coffee and vegetables; Laetisaria fuciformis on turf; Mycosphaerella spp. on bananas, peanuts, citrus, pecans, papaya and other hosts; Diaporthe spp. on citrus, soybean, melon, pears, lupin and other hosts; Elsinoe spp. on citrus, vines, olives, pecans, roses and other hosts; Verticillium spp. on a range of hosts including hops, potatoes and tomatoes; Pyrenopeziza spp. on oil-seed rape and other hosts; Oncobasidium theobromae on cocoa causing vascular streak dieback; Fusarium spp., Typhula spp., Microdochium nivale, Ustilago spp., Urocystis spp., Tilletia spp. and Claviceps purpurea on a variety of hosts but particularly wheat, barley, turf and maize; Ramularia spp. on sugar beet, barley and other hosts; post-harvest diseases particularly of fruit (for example Penicillium digitatum, Penicillium italicum and Trichoderma viride on oranges, Colletotrichum musae and Gloeosporium musarum on bananas and Botrytis cinerea on grapes); other pathogens on vines, notably Eutypa lata, Guignardia bidwellii, Phellinus igniarus, Phomopsis viticola, Pseudopeziza tracheiphila and Stereum hirsutum; other pathogens on trees (for example Lophodermium seditiosum) or lumber, notably Cephaloascus fragrans, Ceratocystis spp., Ophiostoma piceae, Penicillium spp., Trichoderma pseudokoningii, Trichoderma viride, Trichoderma harzianum, Aspergillus niger, Leptographium lindbergi and Aureobasidium pullulans; and fungal vectors of viral diseases (for example Polymyxa graminis on cereals as the vector of barley yellow mosaic virus (BYMV) and Polymyxa betae on sugar beet as the vector of rhizomania). A compound of formula (1) may move acropetally, basipetally or locally in plant tissue to be active against one or more fungi. Moreover, a compound of formula (1) may be volatile enough to be active in the vapour phase against one or more fungi on the plant. The invention therefore provides a method of combating or controlling phytopathogenic fungi which comprises applying a fungicidally effective amount of a compound of formula (1), or a composition containing a compound of formula (1), to a plant, to a seed of a plant, to the locus of the plant or seed or to soil or any other plant growth medium, e.g. nutrient solution. The term "plant" as used herein includes seedlings, bushes and trees. Furthermore, the fungicidal method of the invention includes protectant, curative, systemic, eradicant and antisporulant treatments. The compounds of formula (1) are preferably used for agricultural, horticultural and turfgrass purposes in the form of a composition. In order to apply a compound of formula (1) to a plant, to a seed of a plant, to the locus of the plant or seed or to soil or any other growth medium, a compound of formula (1) is usually formulated into a composition which includes, in addition to the compound of formula (1), a suitable inert diluent or carrier and, optionally, a surface active agent (SFA). SFAs are chemicals that are able to modify the properties of an interface (for example, liquid/solid, liquid/air or liquid/liquid interfaces) by lowering the interfacial tension and thereby leading to changes in other properties (for example dispersion, emulsification and wetting). It is preferred that all compositions (both solid and liquid formulations) comprise, by weight, 0.0001 to 95%, more preferably 1 to 85%, for example 5 to 60%, of a compound of formula (1). The composition is generally used for the control of fungi such that a compound of formula (1) is applied at a rate of from O.lg to 10kg per hectare, preferably from lg to 6kg per hectare, more preferably from lg to 1kg per hectare. When used in a seed dressing, a compound of formula (1) is used at a rate of 0.0001 g to lOg (for example O.OOlg or 0.05g), preferably 0.005g to lOg, more preferably 0.005g to 4g, per kilogram of seed. In another aspect the present invention provides a fungicidal composition comprising a fungi cidally effective amount of a compound of formula (1 ) and a suitable carrier or diluent therefor. In a still further aspect the invention provides a method of combating and controlling fungi at a locus, which comprises treating the fungi, or the locus of the fungi with a fungicidally effective amount of a composition comprising a compound of formula (1). The compositions can be chosen from a number of formulation types, including dustable powders (DP), soluble powders (SP), water soluble granules (SG), water dispersible granules (WG), wettable powders (WP), granules (GR) (slow or fast release), soluble concentrates (SL), oil miscible liquids (OL), ultra low volume liquids (UL), emulsifiable concentrates (EC), dispersible concentrates (DC), emulsions (both oil in water (EW) and water in oil (EO)), micro-emulsions (ME), suspension concentrates (SC), aerosols, fogging/smoke formulations, capsule suspensions (CS) and seed treatment formulations. The formulation type chosen in any instance will depend upon the particular purpose envisaged and the physical, chemical and biological properties of the compound of formula (1). Dustable powders (DP) may be prepared by mixing a compound of formula (1) with one or more solid diluents (for example natural clays, kaolin, pyrophyllite, bentonite, alumina, montmorillonite, kieselguhr, chalk, diatomaceous earths, calcium phosphates, calcium and magnesium carbonates, sulphur, lime, flours, talc and other organic and inorganic solid carriers) and mechanically grinding the mixture to a fine powder. Soluble powders (SP) may be prepared by mixing a compound of formula (1) with one or more water-soluble inorganic salts (such as sodium bicarbonate, sodium carbonate or magnesium sulphate) or one or more water-soluble organic solids (such as a polysaccharide) and, optionally, one or more wetting agents, one or more dispersing agents or a mixture of said agents to improve water dispersibility/solubility. The mixture is then ground to a fine powder. Similar compositions may also be granulated to form water soluble granules (SG). Wettable powders (WP) may be prepared by mixing a compound of formula (1) with one or more solid diluents or carriers, one or more wetting agents and, preferably, one or more dispersing agents and, optionally, one or more suspending agents to facilitate the dispersion in liquids. The mixture is then ground to a fine powder. Similar compositions may also be granulated to form water dispersible granules (WG). Granules (GR) may be formed either by granulating a mixture of a compound of formula (1) and one or more powdered solid diluents or carriers, or from pre-formed blank granules by absorbing a compound of formula (1) (or a solution thereof, in a suitable agent) in a porous granular material (such as pumice, attapulgite clays, fuller's earth, kieselguhr, diatomaceous earths or ground corn cobs) or by adsorbing a compound of formula (1) (or a solution thereof, in a suitable agent) on to a hard core material (such as sands, silicates, mineral carbonates, sulphates or phosphates) and drying if necessary. Agents which are commonly used to aid absorption or adsorption include solvents (such as aliphatic and aromatic petroleum solvents, alcohols, ethers, ketones and esters) and sticking agents (such as polyvinyl acetates, polyvinyl alcohols, dextrins, sugars and vegetable oils). One or more other additives may also be included in granules (for example an emulsifying agent, wetting agent or dispersing agent). Dispersible Concentrates (DC) may be prepared by dissolving a compound of formula (1) in water or an organic solvent, such as a ketone, alcohol or glycol ether. These solutions may contain a surface active agent (for example to improve water dilution or prevent crystallisation in a spray tank). Emulsifiable concentrates (EC) or oil-in-water emulsions (EW) may be prepared by dissolving a compound of formula (1) in an organic solvent (optionally containing one or more wetting agents, one or more emulsifying agents or a mixture of said agents). Suitable organic solvents for use in ECs include aromatic hydrocarbons (such as alkylbenzenes or alkylnaphthalenes, exemplified by SOLVESSO 100, SOLVESSO 150 and SOLVESSO 200; SOLVESSO is a Registered Trade Mark), ketones (such as cyclohexanone or methylcyclo- hexanone), alcohols (such as benzyl alcohol, furfuryl alcohol or butanol), N-alkylpyr- rolidones (such as N-methylpyrrolidone or N-octylpyrrolidone), dimethyl amides of fatty acids (such as C8-Cιo fatty acid dimethyl amide) and chlorinated hydrocarbons. An EC product may spontaneously emulsify on addition to water, to produce an emulsion with sufficient stability to allow spray application through appropriate equipment. Preparation of an EW involves obtaining a compound of formula (1) either as a liquid (if it is not a liquid at room temperature, it may be melted at a reasonable temperature, typically below 70°C) or in solution (by dissolving it in an appropriate solvent) and then emulsifying the resultant liquid or solution into water containing one or more SFAs, under high shear, to produce an emulsion. Suitable solvents for use in EWs include vegetable oils, chlorinated hydrocarbons (such as chlorobenzenes), aromatic solvents (such as alkylbenzenes or alkylnaphthalenes) and other appropriate organic solvents that have a low solubility in water. Microemulsions (ME) may be prepared by mixing water with a blend of one or more solvents with one or more SFAs, to produce spontaneously a thermodynamically stable isotropic liquid formulation. A compound of formula (1) is present initially in either the water or the solvent/SFA blend. Suitable solvents for use in MEs include those hereinbefore described for use in in ECs or in EWs. An ME may be either an oil-in-water or a water-in-oil system (which system is present may be determined by conductivity measurements) and may be suitable for mixing water-soluble and oil-soluble pesticides in the same formulation. An ME is suitable for dilution into water, either remaining as a microemulsion or forming a conventional oil-in-water emulsion. Suspension concentrates (SC) may comprise aqueous or non-aqueous suspensions of finely divided insoluble solid particles of a compound of formula (1). SCs may be prepared by ball or bead milling the solid compound of formula (1) in a suitable medium, optionally with one or more dispersing agents, to produce a fine particle suspension of the compound. One or more wetting agents may be included in the composition and a suspending agent may be included to reduce the rate at which the particles settle. Alternatively, a compound of formula (1) may be dry milled and added to water, containing agents hereinbefore described, to produce the desired end product. Aerosol formulations comprise a compound of formula (1) and a suitable propellant (for example rc-butane). A compound of formula (1) may also be dissolved or dispersed in a suitable medium (for example water or a water miscible liquid, such as n-propanol) to provide compositions for use in non-pressurised, hand-actuated spray pumps. A compound of formula (1) may be mixed in the dry state with a pyrotechnic mixture to form a composition suitable for generating, in an enclosed space, a smoke containing the compound. Capsule suspensions (CS) may be prepared in a manner similar to the preparation of EW formulations but with an additional polymerisation stage such that an aqueous dispersion of oil droplets is obtained, in which each oil droplet is encapsulated by a polymeric shell and contains a compound of formula (1) and, optionally, a carrier or diluent therefor. The polymeric shell may be produced by either an interfacial polycondensation reaction or by a coacervation procedure. The compositions may provide for controlled release of the compound of formula (1) and they may be used for seed treatment. A compound of formula (1) may also be formulated in a biodegradable polymeric matrix to provide a slow, controlled release of the compound. A composition may include one or more additives to improve the biological performance of the composition (for example by improving wetting, retention or distribution on surfaces; resistance to rain on treated surfaces; or uptake or mobility of a compound of formula (1)). Such additives include surface active agents, spray additives based on oils, for example certain mineral oils or natural plant oils (such as soy bean and rape seed oil), and blends of these with other bio-enhancing adjuvants (ingredients which may aid or modify the action of a compound of formula ( 1 )). A compound of formula (1) may also be formulated for use as a seed treatment, for example as a powder composition, including a powder for dry seed treatment (DS), a water soluble powder (SS) or a water dispersible powder for slurry treatment (WS), or as a liquid composition, including a flowable concentrate (FS), a solution (LS) or a capsule suspension (CS). The preparations of DS, SS, WS, FS and LS compositions are very similar to those of, respectively, DP, SP, WP, SC and DC compositions described above. Compositions for treating seed may include an agent for assisting the adhesion of the composition to the seed (for example a mineral oil or a film-forming barrier). Wetting agents, dispersing agents and emulsifying agents may be SFAs of the cationic, anionic, amphoteric or non-ionic type. Suitable SFAs of the cationic type include quaternary ammonium compounds (for example cetyltrimethyl ammonium bromide), imidazolines and amine salts. Suitable anionic SFAs include alkali metals salts of fatty acids, salts of aliphatic monoesters of sulphuric acid (for example sodium lauryl sulphate), salts of sulphonated aromatic compounds (for example sodium dodecylbenzenesulphonate, calcium dodecyl- benzenesulphonate, butylnaphthalene sulphonate and mixtures of sodium di-wopropyl- and tri-z'.sOpropyl-naphthalene sulphonates), ether sulphates, alcohol ether sulphates (for example sodium laureth-3-sulphate), ether carboxylates (for example sodium laureth-3-carboxylate), phosphate esters (products from the reaction between one or more fatty alcohols and phos- phoric acid (predominately mono-esters) or phosphorus pentoxide (predominately di-esters), for example the reaction between lauryl alcohol and tetraphosphoric acid; additionally these products may be ethoxylated), sulphosuccinamates, paraffin or olefine sulphonates, taurates and lignosulphonates. Suitable SFAs of the amphoteric type include betaines, propionates and glycinates. Suitable SFAs of the non-ionic type include condensation products of alkylene oxides, such as ethylene oxide, propylene oxide, butylene oxide or mixtures thereof, with fatty alcohols (such as oleyl alcohol or cetyl alcohol) or with alkylphenols (such as octylphenol, nonylphenol or octylcresol); partial esters derived from long chain fatty acids or hexitol anhydrides; condensation products of said partial esters with ethylene oxide; block polymers (comprising ethylene oxide and propylene oxide); alkanolamides; simple esters (for example fatty acid polyethylene glycol esters); amine oxides (for example lauryl dimethyl amine oxide); and lecithins. Suitable suspending agents include hydrophilic colloids (such as polysaccharides, polyvinylpyrrolidone or sodium carboxymefhylcellulose) and swelling clays (such as bentonite or attapulgite). A compound of formula (1) may be applied by any of the known means of applying fungicidal compounds. For example, it may be applied, formulated or unformulated, to any part of the plant, including the foliage, stems, branches or roots, to the seed before it is planted or to other media in which plants are growing or are to be planted (such as soil surrounding the roots, the soil generally, paddy water or hydroponic culture systems), directly or it may be sprayed on, dusted on, applied by dipping, applied as a cream or paste formulation, applied as a vapour or applied through distribution or incorporation of a composition (such as a granular composition or a composition packed in a water-soluble bag) in soil or an aqueous environment. A compound of formula (1) may also be injected into plants or sprayed onto vegetation using electrodynamic spraying techniques or other low volume methods, or applied by land or aerial irrigation systems. Compositions for use as aqueous preparations (aqueous solutions or dispersions) are generally supplied in the form of a concentrate containing a high proportion of the active ingredient, the concentrate being added to water before use. These concentrates, which may include DCs, SCs, ECs, EWs, MEs SGs, SPs, WPs, WGs and CSs, are often required to withstand storage for prolonged periods and, after such storage, to be capable of addition to water to form aqueous preparations which remain homogeneous for a sufficient time to enable them to be applied by conventional spray equipment. Such aqueous preparations may contain varying amounts of a compound of formula (1) (for example 0.0001 to 10%, by weight) depending upon the purpose for which they are to be used. A compound of formula (1) may be used in mixtures with fertilisers (for example nitrogen-, potassium- or phosphorus-containing fertilisers). Suitable formulation types include granules of fertiliser. The mixtures suitably contain up to 25% by weight of the compound of formula (1). The invention therefore also provides a fertiliser composition comprising a fertiliser and a compound of formula (1). The compositions of this invention may contain other compounds having biological activity, for example micronutrients or compounds having similar or complementary fungicidal activity or which possess plant growth regulating, herbicidal, insecticidal, nematicidal or acaricidal activity. By including another fungicide, the resulting composition may have a broader spectrum of activity or a greater level of intrinsic activity than the compound of formula (1) alone. Further the other fungicide may have a synergistic effect on the fungicidal activity of the compound of formula (1). The compound of formula (1) may be the sole active ingredient of the composition or it may be admixed with one or more additional active ingredients such as a pesticide, fungicide, synergist, herbicide or plant growth regulator where appropriate. An additional active ingredient may: provide a composition having a broader spectrum of activity or increased persistence at a locus; synergise the activity or complement the activity (for example by increasing the speed of effect or overcoming repellency) of the compound of formula (1); or help to overcome or prevent the development of resistance to individual components. The particular additional active ingredient will depend upon the intended utility of the composition. Examples of fungicidal compounds which may be included in the composition of the invention are AC 382042 (N-(l -cyano- l,2-dimethylpropyl)-2-(2,4-dichlorophenoxy) pro- pionamide), acibenzolar-S-methyl, alanycarb, aldimorph, anilazine, azaconazole, azafenidin, azoxystrobin, benalaxyl, benomyl, benthiavalicarb, biloxazol, bitertanol, blasticidin S, boscalid (new name for nicobifen), bromuconazole, bupirimate, captafol, captan, carbendazim, carbendazim chlorhydrate, carboxin, carpropamid, carvone, CGA 41396, CGA 41397, chinomethionate, chlorbenzthiazone, chlorothalonil, chlorozolinate, clozylacon, copper containing compounds such as copper oxychloride, copper oxyquinolate, copper sulphate, copper tallate, and Bordeaux mixture, cyamidazosulfamid, cyazofamid (IKF-916), cyflufenamid, cymoxanil, cyproconazole, cyprodinil, debacarb, di-2-pyridyl disulphide l,l'-dioxide, dichlofluanid, diclocymet, diclomezine, dicloran, diethofencarb, difenoconazole, difenzoquat, diflumetorim, O, O-di-wo-propyl-S-benzyl thiophosphate, dimefluazole, dimetconazole, dimethirimol, dimethomorph, dimoxystrobin, diniconazole, dinocap, dithianon, dodecyl dimethyl ammonium chloride, dodemorph, dodine, doguadine, edifenphos, epoxiconazole, ethaboxam, ethirimol, ethyl (Z)-N-benzyl-N([methyl(methyl- thioethylideneaminooxycarbonyl)amino]thio)-β-alaninate, etridiazole, famoxadone, fenamidone, fenarimol, fenbuconazole, fenfuram, fenhexamid, fenoxanil (AC 382042), fenpiclonil, fenpropidin, fenpropimorph, fen tin acetate, fen tin hydroxide, ferbam, ferimzone, fluazinam, fludioxonil, flumetover, flumorph, fluoroimide, fluoxastrobin, fluquinconazole, flusilazole, flusulfamide, flutolanil, flutriafol, folpet, fosetyl-aluminium, fuberidazole, furalaxyl, furametpyr, guazatine, hexaconazole, hydroxyisoxazole, hymexazole, imazalil, imibenconazole, iminoctadine, iminoctadine triacetate, ipconazole, iprobenfos, iprodione, iprovalicarb, isopropanyl butyl carbamate, isoprothiolane, kasugamycin, kresoxim-methyl, LY186054, LY211795, LY 248908, mancozeb, maneb, mefenoxam, mepanipyrim, mepronil, metalaxyl, metalaxyl M, metconazole, metiram, metiram-zinc, metominostrobin, metra- fenone, MOΝ65500 (N-allyl-4,5-dimethyl-2-trimethylsilylthiophene-3-carboxamide), myc- lobutanil, ΝTΝ0301, neoasozin, nickel dimethyldifhiocarbamate, nitrothale-isopropyl, nuarimol, ofurace, organomercury compounds, orysastrobin, oxadixyl, oxasulfuron, oxolinic acid, oxpoconazole, oxycarboxin, pefurazoate, penconazole, pencycuron, phenazin oxide, phosphorus acids, phthalide, picoxystrobin, polyoxin D, polyram, probenazole, prochloraz, procymidone, propamocarb, propamocarb hydrochloride, propiconazole, propineb, propionic acid, proquinazid, prothioconazole, pyraclostrobin, pyrazophos, pyrifenox, pyrimethanil, pyroquilon, pyroxyfur, pyrrolnitrin, quaternary ammonium compounds, quinomethionate, quinoxyfen, quintozene, silthiofam (MON 65500), S-imazalil, simeconazole, sipconazole, sodium pentachlorophenate, spiroxamine, streptomycin, sulphur, tebuconazole, tecloftalam, tecnazene, tetraconazole, thiabendazole, thifluzamide, 2-(thiocyanomethylthio)- benzothiazole, thiophanate-methyl, thiram, tiadinil, timibenconazole, tolclofos-methyl, tolylfluanid, triadimefon, triadimenol, triazbutil, triazoxide, tricyclazole, tridemorph, trifloxystrobin, triflumizole, triforine, triticonazole, validamycin A, vapam, vinclozolin, XRD-563, zineb, ziram, zoxamide and compounds of the formulae:
Figure imgf000078_0001
The compounds of formula (1) may be mixed with soil, peat or other rooting media for the protection of plants against seed-borne, soil-borne or foliar fungal diseases. Some mixtures may comprise active ingredients, which have significantly different physical, chemical or biological properties such that they do not easily lend themselves to the same conventional formulation type. In these circumstances other formulation types may be prepared. For example, where one active ingredient is a water insoluble solid and the other a water insoluble liquid, it may nevertheless be possible to disperse each active ingredient in the same continuous aqueous phase by dispersing the solid active ingredient as a suspension (using a preparation analogous to that of an SC) but dispersing the liquid active ingredient as an emulsion (using a preparation analogous to that of an EW). The resultant composition is a suspoemulsion (SE) formulation. The invention is illustrated by the following Examples in which the following abbreviations are used: ml = millilitres f = fine g = grammes THF = tetrahydrofuran ppm = parts per million DCM = dichloromethane s = singlet DMF = N, N-dimethylformamide d = doublet DMSO = dimethylsulphoxide t = triplet DMAP = 4-dimethylaminopyridine q = quartet ΝMR = nuclear magnetic resonance m = multiplet HPLC = high performance liquid b = broad chromatography
EXAMPLES
EXAMPLE 1
This example illustrates the preparation of sec-butyl-[6-chloro-7-[(4-fluorophenyl)-2,6- difluorophenyl]-pyrido[2,3-b]pyrazin-8-yl]-amine of the formula below, Compound 3.002.
Figure imgf000079_0001
Step 1: The preparation of 2,6-difluoro-4-bromobenzyl methanesulphonate
2,6-difiuoro-4-bromobenzyl alcohol (9.50 g) and triethylamine (5.0 g) were dissolved in THF cooled to 10°C with stirring. Methanesulphonyl chloride (4.8 g) was added in a solution of THF (10ml) over 10 minutes, and a white solid precipitated from the solution. The reaction was then warmed to room temperature for one hour and then the solid was collected and washed with diethyl ether. The filtrate was evaporated to give 2,6-difluoro-4- bromobenzyl methanesulphonate (13.0 g) as a golden oil which slowly crystallised. 1H NMR (CDC13) δ ppm: 3.05 (s,3H), 5.3 (s,2H), 7.15 (t,2H).
Step 2: The preparation of 2,4-difluoro-4-bromobenzyl cyanide
Potassium cyanide (2.8 g) was dissolved in water and was added to a stirred solution of the product of Step 1 (13.0 g) in ethanol (100 ml). The reaction was refluxed for 2 hours, and was then cooled and the solvent evaporated to give a sludge. Water was added and the mixture was extracted with DCM and dried over magnesium sulphate. The solution was evaporated and to give a sludge which was triturated with a small amount of diethyl ether to give 2,4-difluoro-4-bromobenzyl cyanide as a light brown solid (5.2 g). 1H NMR (CDC13) 6 ppm: 3.7 (s,2H), 7.18 (t,2H).
Step 3: The preparation of 2,6-dfluoro-4-bromophenyl acetic acid
The product from Step 2 (4.2 g) was dissolved in a mixture of water (25 ml) and concentrated sulphuric acid (25 ml), and the reaction was refluxed for 3 hours. The reaction was then cooled and the solid collected was washed with water and dried to give 2,6-dfluoro- 4-bromophenyl acetic acid as a light brown crystalline solid (3.8 g). 1H NMR (CDC13) δ ppm: 3.75 (s,2H), 7.1 (t,2H). Step 4: The preparation of 2,6-dfluoro-4-bromophenyl acetyl chloride
The product from Step 3 (3.6 g) was added portionwise to thionyl chloride (10 ml), preheated to 60°C, with two drops of DMF. Reaction was immediate and after the addition the reaction was refluxed for a further 1 hour, and was then cooled and evaporated to give the acid chloride as a brown liquid (3.6 g), which was used in the next reaction without further purification.
Step 5: The preparation of methyl 3-[2-(4-bromo-2,6-difluoro-phenyl)-acetylamino]- pyrazine-2-carboxylate:
Figure imgf000080_0001
A solution of the crude acid chloride from Step 4 (3.6 g) in DCM (10ml) was added dropwise to a stirred solution of methyl 2-aminopyrazine carboxylate (2.2 g) and pyridine (5 ml) stirred at 10°C in DCM. The reaction was stirred for 15 hours at room temperature, and the solvent was evaporated and water was added, followed by extraction with ethyl acetate. The organic fraction was washed with water and aqueous sodium carbonate, followed by dilute hydrochloric acid. The ethyl acetate was dried over magnesium sulphate and evaporated to give a dark sludge, which was triturated with diethyl ether, and methyl 3-[2-(4- bromo-2,6-difluoro-phenyl)-acetylamino]-pyrazine-2-carboxylate was isolated as a buff solid (2.9 g).
1H NMR (CDC13) δ ppm: 4.0 (s,2H), 4.05 (s,3H), 7.15 (dd,2H), 8.4 (d,lH), 8.6 (d, 1H). Step 6: The preparation of 7-(4-bromo-2,6-difluoro-phenyl)-8-hydroxy-5H-pyrido[2,3-] pyrazin-6-one:
The product from Step 5 (2.9 g) and potassium carbonate (2.1 g) in dry DMF (20 ml) were heated to 100°C (oil bath) for 4 hours, giving a yellow suspension. The solvent was evaporated to dryness and the dark sludge was triturated with diethyl ether, and the pale green solid collected. This solid was dissolved in water and acidified with 4M hydrochloric acid, and the precipitated solid was collected and dried to give 7-(4-bromo-2,6-difluoro- phenyl)-8-hydroxy-5H-pyrido[2,3-]pyrazin-6-one as a buff solid (1.6 g). 1H NMR (CDC13) δ ppm: 7.3 (d,2H), 8.55 (d,lH), 8.65 (d,lH).
Step 7: The preparation of 7-(4-bromo-2,6-difluoro-phenyl)-6,8-dichloro-pyrido[2,3- bjpyrazine
Figure imgf000081_0002
The product from Step 6 (0.353 g) and phosphorus oxychloride (3 ml) were mixed together at room temperature and then refluxed with stirring for 6 hours. The reaction was cooled and evaporated to dryness and water and DCM were added.
The DCM extract was washed with aqueous sodium carbonate, dried with magnesium sulphate, and evaporated to give an oil which was purified by flash column chromatography on silica gel eluting with diethyl ether to give 7-(4-bromo-2,6-difluoro-phenyl)-6,8-dichloro- pyrido[2,3-b]pyrazine as a reddish solid (0.205 g), which was used without further purification. Step 8: The preparation of [7-(4-Bromo-2,6-difluoro-phenyl)-6-chloro-pyrido[2,3-b]pyrazin- 8-yl]-sec-butyl-amine
Figure imgf000082_0001
The product from Step 7 (0.205 g) and s-butylamine (1.0 ml) were mixed together in a sealed tube and were stirred at room temperature for 4 days. The reaction mixture was evaporated to give a sludge, which was then purified by flash column chromatography on silica gel eluting with diethyl etheπhexane 1:2, and then diethyl etheπhexane 4:1, to give [7-(4-Bromo-2,6- difluoro-phenyl)-6-chloro-pyrido[2,3-b]pyrazin-8-yl]-sec-butyl-amine as a yellow solid (0.095 g).
1H NMR (CDCI3) δ ppm: 0.8 (t,3H), 1.1 (d,3H), 1.45 (m,2H), 3.15 (m,2H), 6.95 (bd.lH), 7.3
(d,2H), 8.7 (d,lH), 9.0 (d,lH).
Step 9: The preparation of sec-butyl-[6-chloro-7-[(4-fluorophenyl)-2,6-difluorophenyl]- pyrido[2,3-b]pyrazin-8-yl]-amine, Compound 3.002
The product from Step 8 (0.027 g), 4-fluorophenyl boronic acid (0.012 g), potassium carbonate (0.020 g) and tetrakis(triphenylphosphine)palladium (0.001 g) were mixed and brought to reflux for 6 hours in toluene (2.0 ml). The reaction was cooled and evaporated and the crude product was dissolved in diethyl ether and then purified by flash column chromatography on silica gel eluting with diethyl ether, to give the title product as a white gum (0.010 g).
1H NMR (CDC13) δ ppm: 0.7 (t,3H), 1.1 (d,3H), 1.45 (m,2H), 3.2 (m,lH), 6.95 (bd,lH), 7.15 (d,2H), 7.2 (d,2H), 7.65 (m,2H), 8.7 (d,lH), 9.0 (d,lH).
EXAMPLE 2
This example illustrates the preparation of sec-butyl-[6-chloro-7-[phenyl-2,6- difluorophenyl]-pyrido[2,3-b]pyrazin-8-yl]-amine, Compound 2.002
Figure imgf000083_0001
The compound was prepared analogous to Step 9 from Example 1 from the product of Step 8 of Example 1 , but the coupling reaction was carried out with phenyl boronic acid instead of 4-fluorophenyl boronic acid.
Η NMR (CDC13) δ ppm: 0.75 (t,3H), 1.1 (d,3H),1.45 (m,2H), 3.2 (m,lH), 6.95 (bd,lH), 7.3 (d,2H), 7.45- 7.5 (m,3H), 7.65 (d,2H), 8.65 (fd,lH), 9.0 (fd,lH).
EXAMPLE 3
This example illustrates the preparation of sec-butyl-[6-chloro-7-(2,6-difluoro-(4- methylphenylethynyl)-phenyl)-pyrido[2,3-b]pyrazin-8-yl]-amine of the formula below,
Compound 9.002.
Figure imgf000083_0002
[7-(4-Bromo-2,6-difluoro-phenyl)-6-chloro-pyrido[2,3-b]pyrazin-8-yl]-sec-butyl-amine (0.030 g), 4-methylphenyl acetylene (0.016 g), cuprous iodide (0.001 g), dichlorobis (triphenylphosphine)palladium (0.003 g) and triethylamine (5 ml) were refluxed for 7 hours. The reaction was cooled and evaporated to give a sludge, which was taken up in diethyl ether and purified by flash column chromatography on silica gel eluting with diethyl ether, to give the title compound as a gum (0.008 g).
1H NMR (CDC13) δ ppm: 0.75 (t,3H), 1.05 (d,3H), 1.45 (m,lH), 2.4 (s,3H), 3.15 (m,lH), 6.95 (bd,lH), 7.2 (d,4H), 7.45 (d,2H), 8.15 (bs,lH), 9.0 (bs,lH). EXAMPLE 4 This Example illustrates the fungicidal properties of the compounds of the general formula (1).
Septoria tritici (leaf blotch): Conidia of the fungus from cryogenic storage were directly mixed into nutrient broth (PDB potato dextrose broth). After placing a (DMSO) solution of the test compounds into a microtiter plate (96-well format) the nutrient broth containing the fungal spores was added. The test plates were incubated at 24 C and the inhibition of growth was determined photometrically after 72 hours.
Pyricularia orzyae (rice blast): Conidia of the fungus from cryogenic storage were directly mixed into nutrient broth (PDB potato dextrose broth). After placing a (DMSO) solution of the test compounds into a microtiter plate (96-well format) the nutrient broth containing the fungal spores was added. The test plates were incubated at 24° C and the inhibition of growth was determined photometrically after 72 hours.
The following compounds gave greater than 60% control of disease: Septoria tritici: 2.002 Pyricularia orzyae: 2.002

Claims

CLAΓMS
1. The compound of the general formula ( 1 ) :
Figure imgf000085_0001
wherein
W, X, Y and Z can be N or CR , with at least one and no more than three of W, X, Y and Z being N, but excluding compounds where W, X, Y = N and Z = CR8, and X, Y, Z = N and Z
= CR8;
R8 is H, halo, C1- alkyl, C1-4 alkoxy or halo(C1- )alkyl, CN, C1-4alkylthio, C1- alkylsulphinyl, C1- alkylsulphonyl, aryl, heteroaryl, halo(C1-6)alkoxy, halo(C1- )alkylthiθj C2-4alkenyl, C2 -
6alkynyl, C2-6cycloalkyl, or NR3R4 ;
R is H, Cι-4 alkyl, halo(C1-4)alkyl, cyano, halogen or NR3R4;
R2 is halo or NR3R4;
R1 is an aryl or heteroaryl ring R20, of the general formula
Figure imgf000085_0002
where A can be one to four optional substituents independently selected from halo, C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, C1-6 alkoxy, C2-6 alkenyloxy, C2-6 alkynyloxy, halo(C1- 6)alkyl, halo(C1-6)alkoxy, C1-6 alkylthio, halo(C1-6)alkylthio, C1-4 alkoxy(C1-6)alkyl, C3-6 cycloalkyl, C3-6 cycloalkyl(C1-4)alkyl, and B is at least one or more substituents independently selected from aryl, heteroaryl, aryloxy (except that phenoxy must be substituted), heteroaryloxy, aryl(C1-4)alkoxy (except that benzyloxy must be substituted), heteroaryl(Cj-4)alkoxy, arylthio, arylsulphinyl, arylsulphonyl, heteroarylthio, heteroarylsulphinyl, heteroarylsulphonyl, aryl(C2-4)alkenyl, aryl(C2- )alkynyl, heteroaryl(C2- )alkenyl, heteroaryl(C2-4)alkynyl, aryl(C1- )alkyl, heteroaryl(Cι-4)alkyl, with any of the forgoing aryl or heteroaryl substituents being optionally substituted with halo, C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, -6 alkoxy, C2-6 alkenyloxy, C2_6 alkynyloxy, halo(C1-6)alkyl, halo(C1-6)alkoxy, Cι-6 alkylthio, halo(Cι-6)- alkylthio, C1-4 alkoxy(C1-6)alkyl, C3-6 cycloalkyl, cyano or nitro; R3 and R4 are independently H, C1-8 alkyl, C2-8 alkenyl, C2-8 alkynyl, aryl, aryl(C1-8)alkyl,
C3-8 cycloalkyl, C3-8 cycloalkyl(C1-6)alkyl, heteroaryl, heteroaryl(C1-8)alkyl, NR5R6or
R3 and R4 together form a C3-7 alkylene or C3.7 alkenylene chain optionally substituted with one or more C1-4 alkyl or C1-4 alkoxy groups, or, together with the nitrogen atom to which they are attached, R3 and R4 form a morpholine, thiomoφholine, thiomoφholine S-oxide or thiomoφholine S-dioxide ring or a piperazine or piperazine N-(C1-4)alkyl ring, and R and R are independently H, C1-8 alkyl, C2-8 alkenyl, C - s alkynyl, aryl, aryl(C1-8)alkyl, C3-8 cycloalkyl, C3-8 cycloalkyl(C1-6)alkyl, heteroaryl or heteroaryl(C1-8)alkyl; any of the foregoing alkyl, alkenyl, alkynyl or cycloalkyl groups or moieties (other than for R ) being optionally substituted with halogen, cyano, C1-6 alkoxy, Cι-6 alkylcarbonyl, .6 alkoxycarbonyl, C1-6 haloalkoxy, C1-6 alkylthio, tri(C1- )alkylsilyl, Ci-6 alkylamino or C1-6 dialkylamino, any of the foregoing moφholine, thiomoφholine, piperidine, piperazine and pyrrolidine rings being optionally substituted with C1-4 alkyl (especially methyl), and any of the foregoing aryl or heteroaryl groups or moieties in R3, R4, R , R or R being optionally substituted with one or more substituents selected from halo, hydroxy, mercapto, C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, C1-6 alkoxy, C -6 alkenyloxy, C2-6 alkynyloxy, halo(C1-6)alkyl, halo(C1-6)alkoxy, C1-6 alkylthio, halo(C1-6)alkylthio, hydroxy .. 6)alkyl, C1-4 alkoxy(C1-6)alkyl, C3-6 cycloalkyl, C3-6 cycloalkyl(C1-4)alkyl, phenoxy, benzyloxy, benzoyloxy, cyano, isocyano, thiocyanato, isothiocyanato, nitro, -ΝR13R14, -NHCOR13, -NHCON R13R14, -CON R13R14, -SO2R13, -OSO2 R13, -CO R13, -C R13=N R14 or -N=CR13R14, in which R13 and R14 are independently hydrogen, C alkyl, halo(C1-4)alkyl, C1-4 alkoxy, halo(C1-4)alkoxy, C1-4 alkylthio, C3-6 cycloalkyl, C3-6 cycloalkyl(C1-4)alkyl, phenyl or benzyl, the phenyl and benzyl groups being optionally substituted with halogen, C1-4 alkyl or C1- alkoxy.
2. A compound according to claim 1 wherein W and Z are N and X and Y are CH.
3. A compound according to claim 1 or 2 wherein R2 is NR3R4.
4. A compound according to claim 3 wherein R is halo.
5. A compound according to any one of the preceding claims wherein R3 is C1-8 alkyl, halo(Cι-8)alkyl, halo .4 alkoxy(C1-8)alkyl, C1-4 alkoxyhalo(C1-8)alkyl Cι-4 alkoxycarbonyl(C1-8)alkyl, Cι-4 alkoxycarbonylhalo(C]-8)alkyl, phenyl(1-4)alkyl, C2-8 alkenyl, halo(C -8)alkenyl, C2-8 alkynyl, C3-8 cycloalkyl optionally substituted with chloro, fluoro or methyl, C3-8 cycloalkyl(C1- )alkyl, phenylamino, piperidino or moφholino, the phenyl ring of phenylalkyl or phenylamino being optionally substituted with one, two or three substituents selected from halo, C1- alkyl, halo . 4)alkyl, C1- alkoxy and halo(C].4)alkoxy; and R4 is H, C1-4 alkyl, halo(C1- )alkyl or amino, or R3 and R4 together form a C3- alkylene or alkenylene chain optionally substituted with methyl, or, together with the nitrogen atom to which they are attached, R3 and R4 form a moφholine, thiomoφholine, thiomoφholine S-oxide or thiomoφholine S-dioxide ring or a piperazine or piperazine N-(C1-4)alkyl (especially N-methyl) ring, in which the moφholine or piperazine rings are optionally substituted with methyl.
6. A process for preparing a compound of the general formula (1) according to claim 1 wherein one of R and R2 is chloro or fluoro and the other is ΝR3R4 and W, X, Y, Z, R1, R3 and R4 are as defined in claim 1, which comprises reacting an amine of the general formula NR3R4 with a compound of the general formula (6) or (17):
Figure imgf000087_0001
7. The intermediate chemicals having the general formulae (4), (5), (6), (9), (10), (11), (12), (13) (14) and (17):
Figure imgf000088_0001
Figure imgf000088_0002
(9) (10) (11 )
Figure imgf000088_0003
wherein W, X, Y, Z, R .1 , r R.3 , - Rr.4 , Hal, A and B are as defined in claim 1 and R , is C1-4 alkyl.
8. A plant fungicidal composition comprising a fungicidally effective amount of a compound as defined in claim 1 and a suitable carrier or diluent therefor.
A method of combating or controlling phytopathogenic fungi which comprises applying to a plant, to a seed of a plant, to the locus of the plant or seed or to soil or to any other plant growth medium, a fungicidally effective amount of a compound according to claim 1 or a composition according to claim 15.
PCT/EP2005/006687 2004-06-22 2005-06-21 Fungicides based on nitrogen-containing heterocycles WO2005123698A1 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
US11/570,980 US20080318962A1 (en) 2004-06-22 2005-06-21 Fungicides Based on Nitrogen-Containing Heterocycles
BRPI0512558-8A BRPI0512558A (en) 2004-06-22 2005-06-21 chemical compounds
JP2007517181A JP2008503527A (en) 2004-06-22 2005-06-21 Bactericides based on nitrogen-containing heterocycles
EP05753230A EP1771423A1 (en) 2004-06-22 2005-06-21 Fungicides based on nitrogen-containing heterocycles

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB0413955.6 2004-06-22
GBGB0413955.6A GB0413955D0 (en) 2004-06-22 2004-06-22 Chemical compounds

Publications (1)

Publication Number Publication Date
WO2005123698A1 true WO2005123698A1 (en) 2005-12-29

Family

ID=32799948

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2005/006687 WO2005123698A1 (en) 2004-06-22 2005-06-21 Fungicides based on nitrogen-containing heterocycles

Country Status (6)

Country Link
US (1) US20080318962A1 (en)
EP (1) EP1771423A1 (en)
JP (1) JP2008503527A (en)
BR (1) BRPI0512558A (en)
GB (1) GB0413955D0 (en)
WO (1) WO2005123698A1 (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007088060A1 (en) * 2006-02-03 2007-08-09 Syngenta Participations Ag Tetrahydropyrido [2, 3-b] pyrazine and dihydropyrido [2 , 3-b] pyrazine derivatives as plant fungicides
WO2008009908A1 (en) * 2006-07-20 2008-01-24 Syngenta Limited Pyrido [2, 3-b] pyrazine derivatives useful as herbicidal compounds
US7323468B2 (en) 2003-05-23 2008-01-29 Aeterna Zentaris Gmbh Pyridopyrazines and the use thereof as kinase inhibitors
WO2008071918A1 (en) * 2006-12-12 2008-06-19 Syngenta Limited Pyrido-pyrazine derivatives useful as herbicidal compounds
WO2011022473A1 (en) 2009-08-19 2011-02-24 Ambit Biosciences Corporation Biaryl compounds and methods of use thereof
US8217042B2 (en) 2005-11-11 2012-07-10 Zentaris Gmbh Pyridopyrazines and their use as modulators of kinases
US8937068B2 (en) 2005-11-11 2015-01-20 Zentaris Gmbh Pyridopyrazine derivatives and their use

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0413953D0 (en) * 2004-06-22 2004-07-28 Syngenta Participations Ag Chemical compounds

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4801592A (en) * 1986-12-31 1989-01-31 Basf Aktiengesellschaft Substituted 1,8-naphthyridine derivatives and fungicides containing them
WO2004056825A1 (en) * 2002-12-23 2004-07-08 Syngenta Limited Pyridodiazines as plant fungicides
WO2004056829A1 (en) * 2002-12-23 2004-07-08 Syngenta Limited Fungicides based on nitrogen-containing heterocycles
WO2004056826A1 (en) * 2002-12-23 2004-07-08 Syngenta Limited Fungicides
WO2004056824A2 (en) * 2002-12-23 2004-07-08 Syngenta Limited Naphthyridine derivatives and their use as fungicides

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3984412A (en) * 1974-07-25 1976-10-05 E. R. Squibb & Sons, Inc. Amino derivatives of pyrido[2,3-b]pyrazine carboxylic acids and esters
GB0413953D0 (en) * 2004-06-22 2004-07-28 Syngenta Participations Ag Chemical compounds

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4801592A (en) * 1986-12-31 1989-01-31 Basf Aktiengesellschaft Substituted 1,8-naphthyridine derivatives and fungicides containing them
WO2004056825A1 (en) * 2002-12-23 2004-07-08 Syngenta Limited Pyridodiazines as plant fungicides
WO2004056829A1 (en) * 2002-12-23 2004-07-08 Syngenta Limited Fungicides based on nitrogen-containing heterocycles
WO2004056826A1 (en) * 2002-12-23 2004-07-08 Syngenta Limited Fungicides
WO2004056824A2 (en) * 2002-12-23 2004-07-08 Syngenta Limited Naphthyridine derivatives and their use as fungicides

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7323468B2 (en) 2003-05-23 2008-01-29 Aeterna Zentaris Gmbh Pyridopyrazines and the use thereof as kinase inhibitors
US8937068B2 (en) 2005-11-11 2015-01-20 Zentaris Gmbh Pyridopyrazine derivatives and their use
US8217042B2 (en) 2005-11-11 2012-07-10 Zentaris Gmbh Pyridopyrazines and their use as modulators of kinases
WO2007088060A1 (en) * 2006-02-03 2007-08-09 Syngenta Participations Ag Tetrahydropyrido [2, 3-b] pyrazine and dihydropyrido [2 , 3-b] pyrazine derivatives as plant fungicides
US8133847B2 (en) 2006-07-20 2012-03-13 Syngenta Limited Pyrido[2,3-B]pyrazine derivatives useful as herbicidal compounds
WO2008009908A1 (en) * 2006-07-20 2008-01-24 Syngenta Limited Pyrido [2, 3-b] pyrazine derivatives useful as herbicidal compounds
JP2009544601A (en) * 2006-07-20 2009-12-17 シンジェンタ リミテッド Pyrido [2,3-b] pyrazine derivatives useful as herbicidal compounds
AU2007274910B2 (en) * 2006-07-20 2012-07-26 Syngenta Limited Pyrido [2, 3-b] pyrazine derivatives useful as herbicidal compounds
EA016143B1 (en) * 2006-07-20 2012-02-28 Зингента Лимитед Pyrido [2, 3-b] pyrazine derivatives useful as herbicidal compounds
WO2008071918A1 (en) * 2006-12-12 2008-06-19 Syngenta Limited Pyrido-pyrazine derivatives useful as herbicidal compounds
US8217055B2 (en) 2006-12-12 2012-07-10 Syngenta Crop Protection Llc Pyrido-pyrazine derivatives useful as herbicidal compounds
EA015647B1 (en) * 2006-12-12 2011-10-31 Синджента Лимитед Pyrido-pyrazine derivatives useful as herbicidal compounds
JP2010512375A (en) * 2006-12-12 2010-04-22 シンジェンタ リミテッド Pyrido-pyrazine derivatives useful as herbicidal compounds
WO2011022473A1 (en) 2009-08-19 2011-02-24 Ambit Biosciences Corporation Biaryl compounds and methods of use thereof

Also Published As

Publication number Publication date
JP2008503527A (en) 2008-02-07
BRPI0512558A (en) 2008-03-25
GB0413955D0 (en) 2004-07-28
EP1771423A1 (en) 2007-04-11
US20080318962A1 (en) 2008-12-25

Similar Documents

Publication Publication Date Title
US20090069333A1 (en) Fungicides
EP2231614B1 (en) Quinoline derivatives and their use as fungicides
US8440595B2 (en) Fungicides
US20080280766A1 (en) Pyridopyrazines for Combating Phytopathogenic Fungi
US20080287472A1 (en) Fungicides
US20080318962A1 (en) Fungicides Based on Nitrogen-Containing Heterocycles
EP1585746B1 (en) Naphthyridine derivatives and their use as fungicides
EP1575956B1 (en) Fungicides based on nitrogen-containing heterocycles
WO2003039259A1 (en) Fungicides
US20140045890A1 (en) Novel compounds
WO2014044642A1 (en) N-cyclopropylmethyl-2-(quinolin-6-yloxy)-acetamide derivatives and their use as fungicides
WO2011154240A1 (en) Quinoline derivatives as fungicides

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BW BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE EG ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KM KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NA NG NI NO NZ OM PG PH PL PT RO RU SC SD SE SG SK SL SM SY TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): GM KE LS MW MZ NA SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LT LU MC NL PL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
WWE Wipo information: entry into national phase

Ref document number: 2005753230

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 2007517181

Country of ref document: JP

NENP Non-entry into the national phase

Ref country code: DE

WWW Wipo information: withdrawn in national office

Country of ref document: DE

WWP Wipo information: published in national office

Ref document number: 2005753230

Country of ref document: EP

ENP Entry into the national phase

Ref document number: PI0512558

Country of ref document: BR

WWE Wipo information: entry into national phase

Ref document number: 11570980

Country of ref document: US