Title of Invention	FUNGICIDAL MIXTURE COMPRISING AZOLOPYRIMIDINYLAMINES AND ANOTHER ACTIVE COMPOUND
Abstract	Fungicidal mixtures comprising, as active components, 1) azolopyrimidinylamines of the formula I, in which the substituents are as defined in the description and 2) at least one active compound II selected from the following groups: azoles, strobilurins, carboxamides, heterocylic compounds, carbamates and other active compounds selected from the group consisting of guanidines, antibiotics, sulfur-containing heterocyclyl compounds, organophosphorus compounds, organochlorine compounds, inorganic active compounds, growth retardants and cyflufenamid, cymoxanil, dimethirimol, ethirimol, furalaxyl, metrafenone and spiroxamine; in a synergistically effective amount. Methods for controlling harmful fungi using mixtures of the compound I with active compounds II and the use of the compound I with active compounds II for preparing such mixtures, and also compositions comprising these mixtures.

Title of Invention

FUNGICIDAL MIXTURE COMPRISING AZOLOPYRIMIDINYLAMINES AND ANOTHER ACTIVE COMPOUND

Abstract

Fungicidal mixtures comprising, as active components, 1) azolopyrimidinylamines of the formula I, in which the substituents are as defined in the description and 2) at least one active compound II selected from the following groups: azoles, strobilurins, carboxamides, heterocylic compounds, carbamates and other active compounds selected from the group consisting of guanidines, antibiotics, sulfur-containing heterocyclyl compounds, organophosphorus compounds, organochlorine compounds, inorganic active compounds, growth retardants and cyflufenamid, cymoxanil, dimethirimol, ethirimol, furalaxyl, metrafenone and spiroxamine; in a synergistically effective amount. Methods for controlling harmful fungi using mixtures of the compound I with active compounds II and the use of the compound I with active compounds II for preparing such mixtures, and also compositions comprising these mixtures.

Full Text	PF 56951 1 Fungicidal mixtures based on azolopyrimidinylamines Description The present invention relates to fungicidal mixtures comprising, as active components, 1) azolopyrimidinylamines of the formula I, in which the substituents are as defined below: R1 is C3-C12-alkyl, C2-C12-alkenyl, C5-C12-alkoxyalkyl, C3-C6-cycloalkyl, phenyl or phenyl-C1-C4-alkyl; R2 is C1-C12-alkyl, C2-C12-alkenyl, C1-C4-haloalkyl, C1-C4-alkoxy-C1-C4-alkyl; where the aliphatic chains in R1 and/or R2 may be substituted by one to four identical or different groups Ra: Ra is halogen, cyano, hydroxyl, mercapto, C1-C10-alkyl, C1-C10-haloalkyl, C3-C6-cycloalkyl, C2-C10-alkenyl, C2-C10-alkynyl, C1-C6-alkoxy, C1-C6- alkylthio, C1-C6-alkoxy-C1-C6-alkyl or NRARB; RA, RB are hydrogen and C1-C6-alkyl; where the cyclic groups in R1 and/or Ra may be substituted by one to four groups Rb: Rb is halogen, cyano, hydroxyl, mercapto, nitro, NRARB, C1-C10-al- kyl, C1-C6-haloalkyl, C2-C6-alkenyl, C2-C6-alkynyl or C1-C6- alkoxy; R3 is hydrogen, halogen, cyano, NRARB, hydroxyl, mercapto, C1-C6-alkyl, C1- C6-haloalkyl, C3-C8-cycloalkyl, C1-C6-alkoxy, C1-C6-alkylthio, C3-C8- cycloalkoxy, C3-C5-cycloalkylthio. carboxyl, formyl, C1-C10-alkylcarbonyl, C1- C10-alkoxycarbonyl, C2-C10-alkenyloxycarbonyl, C2-C10-alkynyloxycarbonyl, phenyl, phenoxy, phenylthio, benzyloxy, benzylthio, C1-C6-alkyl-S(O)m-; m is 0, 1 or 2; A is CH or N; and 2) at least one active compound II selected from the following groups: PF 56951 2 A) azoles, such as bitertanol, bromuconazole, cyproconazole, difenoconazole, diniconazole, enilconazole, epoxiconazole, fluquinconazole, fenbuconazole, flusilazole, flutriafol, hexaconazole, imibenconazole, ipconazole, metconazole, myclobutanil, penconazole, propiconazole, prothioconazole, simeconazole, triadimefon, triadimenol, tebuconazole, tetraconazole, triticonazole; prochloraz, pefurazoate, imazalil, triflumizole, cyazofamid; benomyl, carbendazim, thiabendazole, fuberidazole; ethaboxam, etridiazole, hymexazole; B) strobilurins, such as azoxystrobin, dimoxystrobin, enestroburin, fluoxa- strobin, kresoxim-methyl, metominostrobin, orysastrobin, picoxystrobin, pyraclostrobin, trifloxystrobin, or methyl (2-chloro-5-[1-(3-methylbenzyl- oxyimino)ethyl]benzyl)carbamate, methyl (2-chloro-5-[1-(6-methylpyridin-2- ylmethoxyimino)ethyl]benzyl)carbamate, methyl 2-(ortho-((2,5-di- methylphenyloxymethylene)phenyl)-3-methoxyacrylate; C) carboxamides, such as carboxin, benalaxyl, boscalid, fenhexamid, flutolanil, furametpyr, mepronil, metalaxyl, mefenoxam, ofurace, oxadixyl, oxycarboxin, penthiopyrad, thifluzamide, tiadinil, N-(4'-bromobiphenyl-2-yl)- 4-difluoromethyl-2-methylthiazole-5-carboxamide, N-(4'- trifluoromethylbiphenyl-2-yl)-4-difluoromethyl-2-methylthiazole-5- carboxamide, N-(4'-chloro-3'-fluorobiphenyl-2-yl)-4-difluoromethyl-2- methylthiazole-5-carboxamide, N-(3',4'-dichloro-4-fluorobiphenyl-2-yl)-3- difluoromethyl-1-methylpyrazole-4-carboxamide, N-(3',4'-dichloro-5- fluorobiphenyl-2-yl)-3-difluoromethyl-1-methylpyrazole-4-carboxamide; 3,4-dichloro-N-(2-cyanophenyl)isothiazol-5-carboxamjde; dimethomorph, flumorph; flumetover, fluopicolide (picobenzamid), zoxamide; carpropamid, diclocymet, mandipropamid; N-(2-{4-[3-(4-chlorophenyl)prop-2-ynyloxy]-3-methoxyphenyl}ethyl)-2- methanesulfonylamino-3-methylbutyramide, N-(2-{4-[3-(4-chlorophenyl)- prop-2-ynyloxy]-3-methoxyphenyl}ethy!)-2-ethanesulfonylamino-3-methyl- butyramide; D) heterocylic compounds, such as fluazinam, pyrifenox; bupirimate, cyprodinil, fenarimol, ferimzone, mepanipyrim, nuarimol, pyrimethanil; triforine; fenpiclonil, fludioxonil; aldimorph, dodemorph, fenpropimorph, tridemorph; fenpropidin, iprodione, procymidone, vinclozolin; PF 56951 3 famoxadone, fenamidone, octhilinone, probenazole; amisulbrom, anilazine, diclomezine, pyroquilon, proquinazid, tricyclazole; 5-chloro-7-(4-methylpiperidin-1 -yl)-6-(2,4,6-trifluorophenyl)-[1,2,4]tri- azolo[1,5-a]pyrimidine, 2-butoxy-6-iodo-3-propylchromen-4-one; acibenzolar-S-methyl, captafol, captan, dazomet, folpet, fenoxanil, quin- oxyfen; 3-[5-(4-chlorophenyl)-2,3-dimethylisoxazolidin-3-yl]pyridine; E) carbamates, such as mancozeb, maneb, metam, metiram, ferbam, propineb, thiram, zineb, ziram; diethofencarb, iprovalicarb, flubenthiavalicarb, propamocarb; methyl 3-(4-chlorophenyl)-3-(2-isopropoxycarbonylamino-3-methyl- butyrylamino)propanoate; and F) other active compounds, such as guanidines: dodine, iminoctadine, guazatine; antibiotics: kasugamycin, streptomycin, polyoxine, validamycin A; nitrophenyl derivates: binapacryl, dinocap, dinobuton; sulfur-containing heterocyclyl compounds: dithianon, isoprothiolane; organometal compounds: fentin salts, such as fentin-acetate; organophosphorus compounds: edifenphos, iprobenfos, fosetyl, fosetyl- aluminum, phosphorous acid and its salts, pyrazophos, tolclofos-methyl; organochlorine compounds: chlorothalonil, dichlofluanid, flusulfamide, hexachlorobenzene, phthalide, pencycuron, quintozene, thiophanate- methyl, tolylfluanid; inorganic active compounds: Bordeaux mixture, copper acetate, copper hydroxide, copper oxychloride, basic copper sulfate, sulfur; others: cyflufenamid, cymoxanil, dimethirimol, ethirimol, furalaxyl, metrafenone and spiroxamine; growth retardants: prohexadione and its salts, trinexapac-ethyl, chlormequat, mepiquat-chloride and diflufenzopyr; in a synergistically effective amount. Moreover, the invention relates to a method for controlling harmful fungi using mixtures of the compound I with active compounds II and to the use of the compound I with active compounds II for preparing such mixtures, and also to compositions comprising these mixtures. The azolopyrimidin-7-ylamines of the formula I referred to above as component 1, their preparation and their action against harmful fungi are known from the literature (EP-A 71 792; EP-A 141 317; WO 03/009687; WO 05/087771; WO 05/087772; WO PF 56951 4 05/087773; PCT/EP/05/002426; PCT/EP2006/050922; PCT/EP2006/060399. The active compounds II mentioned above as component 2, their preparation and their action against harmful fungi are generally known (cf.: http://www.hclrss.demon.co.uk/index.html); they are commercially available. bitertanol, (3-([1,1'-biphenyl]-4-yloxy)-a-(1,1-dimethylethyl)-1 H-1,2,4-triazole-1-ethanol (DE 23 24 020), bromuconazole, 1-[[4-bromo-2-(2,4-dichlorophenyl)tetrahydro-2-furanyl]methyl]-1H 1,2,4-triazole (Proc. 1990 Br. Crop. Prot. Conf. - Pests Dis. Vol. 1, p. 459); cyproconazole, 2-(4-chlorophenyl)-3-cyclopropyl-1 -[1,2,4]triazol-1-ylbutan-2-ol (US 4 664 696); difenoconazole, 1-{2-[2-chloro-4-(4-chlorophenoxy)phenyl]-4-methyl-[1,3]dioxolan-2- ylmethyl}-1H-[1,2,4]triazole (GB-A 2 098 607); diniconazole, (βE)-β-[(2,4-dichlorophenyl)methylene]-α-(1,1-dimethylethyl)-1H-1,2,4- triazole-1-ethanol (Noyaku Kagaku, 1983, Vol. 8, p. 575); enilconazole (imazalil), 1-[2-(2,4-dichlorphenyl)-2-(2-propenyloxy)ethyl]-1H-imidazole (Fruits, 1973, Vol. 28, p. 545); epoxiconazole, (2RS,3SR)-1-[3-(2-chlorophenyl)-2,3-epoxy-2-(4-fiuorophenyl)propyl]- 1 H-1,2,4-triazole (EP-A 196 038); fluquinconazole, 3-(2,4-dichlorophenyl)-6-fiuoro-2-[1,2,4]-triazol-1 -yl-3H-quinazolin-4- one (Proc. Br. Crop Prot. Conf.-Pests Dis., 5-3, 411 (1992)); fenbuconazole, a-[2-(4-chlorophenyl)ethyl]-a-phenyl-1 H-1,2,4-triazole-1 -propanenitrile (Proc. 1988 Br. Crop Prot. Conf. - Pests Dis. Vol. 1, p. 33); flusilazole, 1-{[bis-(4-fluorophenyl)methy!silanyl]methyl}-1H-[1,2,4]triazole (Proc. Br. Crop Prot. Conf.-Pests Dis., 1, 413 (1984)); flutriafol, α-(2-fluorophenyl)-α-(4-fluorophenyl)-1H-1,2,4-triazole-1-ethanol (EP 15 756); hexaconazole, 2-(2,4-dichlorophenyl)-1-[1,2,4]triazol-1-ylhexan-2-ol (CAS RN 79983-71-4); imibenconazole, (4-chlorophenyl)methyl N-(2,4-dichlorophenyl)-1 H-1,2,4-triazole-1 - ethanimidothioate ((Proc. 1988 Br. Crop Prot. Conf. - Pests Dis. Vol. 2, p. 519), imidothioate ((Proc. 1988 Br. Crop Prot. Conf. - Pests Dis. Vol. 2, p. 519), ipconazole, 2-[(4-chlorophenyl)methyl]-5-(1-methylethyl)-1-(1 H-1,2,4-triazol-1-yl- methyl)cyclopentanol (EP 267 778), metconazole, 5-(4-chlorobenzyl)-2,2-dimethyl-1 -[1,2,4]triazol-1 -ylmethylcyclopentanol (GB 857 383); myclobutanil, 2-(4-chlorophenyl)-2-[1,2,4]triazol-1-ylmethylpentanenitrile (CAS RN 88671-89-0); penconazole, 1-[2-(2,4-dichlorophenyl)pentyl]-1H-[1,2,4]triazole (Pesticide Manual, 12th Ed. (2000), p.712); propiconazole, 1-[[2-(2,4-dichlorophenyi)-4-propyl-1,3-dioxolan-2-yl]methyl]-1 H-1,2,4- triazole (BE 835 579); prothioconazole, 2-[2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-2,4- PF 56951 5 dihydro-[1,2,4]triazole-3-thione (WO 96/16048); simeconazole, α-(4-fluorophenyl)-α-[(trimethylsilyl)methyl]-1H-1,2,4-triazole-1-ethanol [CAS RN 149508-90-7], triadimefon, 1-(4-chlorophenoxy)-3,3-dimethyl-1-(1 H-1,2,4-triazol-1-yl)-2-butanone; triadimenol, β-(4-chlorophenoxy)α-(1,1-dimethylethy)-1H-triazole-1-ethanol; tebuconazole, 1-(4-chlorophenyl)-4,4-dimethyl-3-[1,2,4]triazol-1-ylmethylpentan-3-ol (EP-A 40 345); tetraconazole, 1-[2-(2,4-dichlorophenyl)-3-(1,1,2,2-tetrafluoroethoxy)propyl]-1 H-1,2,4- triazole (EP 234 242); triticonazole, (5E)-5-[(4-chlorophenyl)methylene]-2,2-dimethyl-1-(1H-1,2,4-triazol-1- ylmethyl)cyclopentanol (FR 26 41 277); prochloraz, N-{propyl-[2-(2,4,6-trichlorophenoxy)ethyl]}imidazole-1 -carboxamide (US 3 991 071); pefurazoate, 4-pentenyl 2-[(2-furanylmethyl)(1 H-imidazol-1-ylcarbonyl)amino]butanoate [CAS RN 101903-30-4], triflumizole, (4-chloro-2-trifluoromethylphenyl)-(2-propoxy-1 -[1,2,4]triazol-1 -ylethyli- dene)amine (JP-A 79/119 462) cyazofamid, 4-chloro-2-cyano-N',N-dimethyl-5-(4-methylphenyl)-1 H-imidazole-1 -sulfon- amide (CAS RN 120116-88-3], benomyl, N-butyl-2-acetylaminobenzoimidazol-1-carboxamide (US 3 631 176); carbendazim, methyl (1H-benzoimidazol-2-yl)-carbamate (US 3 657 443); thiabendazole, 2-(1,3-thiazol-4-yl)benzimidazole (US 3 017 415), fuberidazole, 2-(2-furanyl)-1H-benzimidazole (DE 12 09 799), ethaboxam, N-(cyano-2-thienylmethyl)-4-ethyl-2-(ethylamino)-5-thiazolcarboxamide (EP-A 639 574), etridiazole, hymexazole, 5-methyl-1,2-oxazol-3-ol (JP 518249, JP 532202), azoxystrobin, methyl 2-{2-[6-(2-cyano-1-vinylpenta-1,3-dienyloxy)pyrimidin-4- yloxy]phenyl}-3-rnethoxyacrylate (EP-A 382 375), dimoxystrobin, (E)-2-(methoxyimino)-AAmethyl-2-[α-(2,5-xylyloxy)-o-tolyl]acetamide (EP-A 477 631); fluoxastrobin, (E)-{2-[6-(2-chlorophenoxy)-5-fluoropyrimidin-4-yIoxy]phenyl}(5,6- dihydro-1,4,2-dioxazin-3-yl)methanone O-methy!oxime (WO 97/27189); kresoxim-methyl, methyl (E)-methoxyimino[α-(o-tolyloxy)-o-tolyl]acetate (EP-A 253 213); metominostrobin, (E)-2-(methoxyimino)-N-methyl-2-(2-phenoxyphenyl)acetamide (EP- A 398 692); orysastrobin, (2E)-2-(methoxyimino)-2-{2-[(3E,5E,6E)-5-(methoxyimino)-4,6-dimethyl- 2,8-dioxa-3,7-diazanona-3,6-dien-1-yl]phenyl}-N-methylacetamide (WO 97/15552); picoxystrobin, methyl 3-methoxy-2-[2-(6-trifluoromethylpyridin-2-yloxymethyl)phenyl]- acrylate (EP-A 278 595); pyraclostrobin, methyl N-{2-[1-(4-chlorophenyl)-1H-pyrazol-3-yloxymethyl]phenyl}(N- PF 56951 6 methoxy)carbamate (WO-A 96/01256); trifloxystrobin, methyl (E)-methoxyimino-{(E)-α-[1-(α,α,α-trifluoro-m-tolyl)ethylidene- aminooxy]-o-tolyl}acetate (EP-A 460 575); carboxin, 5,6-dihydro-2-methyl-N-phenyl-1,4-oxathiin-3-carboxamide (US 3 249 499), benalaxyl, methyl N-(phenylacetyl)-N-(2,6-xylyl)-DL-alaninate (DE 29 03 612), boscalid, 2-chloro-N-(4'-chlorbiphenyl-2-yl)nicotinamide (EP-A 545 099); fenhexamid, N-(2,3-dichloro-4-hydroxyphenyl)-1-methylcyclohexanecarboxamide (Proc. Br. Crop Prot. Conf. - Pests Dis., 1998, Vol. 2, p. 327); flutolanil, a,a,a-trifluoro-3'-isopropoxy-otoluanilide (JP 1104514), furametpyr, 5-chloro-N-(1,3-dihydro-1,1,3-trimethyl-4-isobenzofuranyl)-1,3-dimethyl-1 H- pyrazole-4-carboxamide [CAS RN 123572-88-3], mepronil, 3'-isopropoxy-o-toluanilide (US 3 937 840), metalaxyl, methyl N-(methoxyacetyl)-N-(2,6-xylyl)-DL-alaninate (GB 15 00 581); mefenoxam, methyl N-(2,6-dimethylphenyl)-N-(methoxyacetyl)-D-alaninate; ofurace, (RS)-α-(2-chloro-N-2,6-xylylacetamido)-Y-butyrolactone [CAS RN 58810-48-3]; oxadixyl; N-(2,6-dimethylphenyl)-2-methoxy-N-(2-oxo-3-oxazolidinyl)acetamide (GB 20 58 059), oxycarboxin, 5,6-dihydro-2-methyl-1,4-oxathiin-3-carboxanilide 4,4-dioxide (US 3 399 214), penthiopyrad, N-[2-(1,3-dimethylbutyl)-3-thienyl]-1-methyl-3-(trifluoromethyl)-1 H- pyrazole-4-carboxamide (JP 10130268), thifluzamide, N-[2,6-dibromo-4-(trifluoromethoxy)phenyl]-2-methyl-4-(trifluoromethyl)-5- thiazolecarboxamide; tiadinil, 3'-chloro-4,4'-dimethyl-1,2,3-thiadiazole-5-carboxanilide [CAS RN 223580-51- 6], dimethomorph, 3-(4-chlorophenyl)-3-(3,4-dimethoxyphenyl)-1-morpholin-4-ylpropenone (EP-A 120 321); flumorph, 3-(4-fluorophenyl)-3-(3,4-dimethoxyphenyl)-1-morpholin-4-ylpropenone (EP- A 860 438); flumetover, 2-(3,4-dimethoxyphenyl)-N-ethyl-a,a,a-trifluoro-N-methyl-p-toluamide [AGROWNo. 243, 22(1995)], fluopicolide (picobenzamid), 2,6-dichloro-N-(3-chloro-5-trifluoromethylpyridin-2- ylmethyl)benzamide (WO 99/42447); zoxamide, (RS)-3,5-dichloro-N-(3-chloro-1-ethyl-1-methyl-2-oxopropyl)-p-toluamide [CAS RN 156052-68-5]; carpropamid, 2,2-dichloro-N-[1 -(4-chlorophenyl)ethyl]-1 -ethyl-3-methylcyclopropane- carboxamide [CAS RN 104030-54-8], diclocymet, 2-cyano-N-[(1R)-1-(2,4-dichlorophenyl)ethyl]-3,3-dimethyl butanamide; mandipropamid, (RS)-2-(4-chlorophenyl)-N-[3-methoxy-4-(prop-2-ynyloxy)phenethyl]-2- (prop-2-ynyloxy)acetamide [CAS RN 374726-62-2]; fluazinam, 3-chloro-N-[3-chloro-2,6-dinitro-4-(trifluoromethyl)phenyl]-5-(trifluoromethyl)- 2-pyridinamine (The Pesticide Manual, publ. The British Crop Protection Council, 10th PF 56951 7 ed. (1995), p. 474); pyrifenox, 1-(2,4-dichlorophenyl)-2-(3-pyridinyl)ethanone O-methyloxime (EP-A 49 854); bupirimate, 5-butyl-2-ethylamino-6-methylpyrimidin-4-yldimethylsulfamate [CAS RN 41483-43-6]; cyprodinil, (4-cyclopropyl-6-methylpyrimidin-2-yl)phenylamine (EP-A 310 550); fenarimol, (4-chlorophenyl) (2-chlorophenyl) pyrimidin-5-ylmethanol (GB 12 18 623); ferimzone, (Z)-2'-methylacetophenone 4,6-dimethylpyrimidin-2-ylhydrazone [CAS RN 89269-64-7]; mepanipyrim, (4-methyl-6-prop-1-ynylpyrimidin-2-yl)phenylamine (EP-A 224 339); nuarimol, α-(2-chlorophenyl)-α-(4-fluorophenyl)-5-pyrimidinemethanol (GB 12 18 623); pyrimethanil, 4,6-dimethylpyrimidin-2-ylphenylamine (DD-A 151 404); triforine, N,N-{piperazine-1,4-diylbis[(trichloromethyl)methylene]}diformamide (DE 19 01 421); fenpiclonil, 4-(2,3-dichlorophenyl)-1H-pyrrole-3-carbonitrile (Proc. 1988 Br. Crop Prot. Conf. - Pests Dis., Vol. 1, p. 65); fludioxonil, 4-(2,2-difluorobenzo[1,3]dioxol-4-yl)-1H-pyrrole-3-carbonitrile (The Pesticide Manual, publ. The British Crop Protection Council, 10th ed. (1995), p. 482); aldimorph, 4-alkyl-2,5(or 2,6)-dimethylmorpholine, comprising 65-75% of 2,6-dimethyl- morpholine and 25-35% of 2,5-dimethylmorpholine, comprising more than 85% of 4- dodecyl-2,5(or 2,6)-dimethylmorpholine, where "alkyl" may also include octyl, decyl, tetradecyl or hexadecyl and where the cis/trans ratio is 1:1; dodemorph, 4-cyclododecyl-2,6-dimethylmorpholine (DE 1198125); fenpropimorph, (RS)-cis-4-[3-(4-tert-butylphenyl)-2-methylpropyl]-2,6-dimethyl- morpholine (DE 27 52 096); tridemorph, 2,6-dimethyl-4-tridecylmorpholine (DE 11 64 152); fenpropidin, (RS)-1-[3-(4-tert-butylphenyl)-2-methylpropyl]piperidine (DE 27 52 096); iprodione, N-isopropyl-3-(3,5-dichlorophenyl)-2,4-dioxoimidazolidine-1-carboxamide (GB 13 12 536); procymidone, N-(3,5-dichlorophenyl)-1,2-dimethylcyclopropane-1,2-dicarboximide (US 3 903 090); vinclozolin, 3-(3,5-dichlorophenyl)-5-methyl-5-vinyloxazolidine-2,4-dione (DE-OS 22 07 576); famoxadone, (RS)-3-anilino-5-methyl-5-(4-phenoxyphenyl)-13-oxazolidine-24-dione; fenamidone, (S)-1-anilino-4-methyl-2-methylthio-4-phenylimidazolin-5-one; octhilinone, probenazole, 3-allyloxy-1,2-benzothiazole 1,1-dioxide; amisulbrom, N,N-dimethyl-3-(3-bromo-6-fluoro-2-methylindole-1-sulfonyl)- [1,2,4]triazole-1-sulfonamide (WO 03/053145); anilazine, 4,6-dichloro-N-(2-chlorophenyl)-1,3,5-triazine-2-amine (US 2 720 480); diclomezine, 6-(3,5-dichlorophenyl)-p-tolyl)pyridazin-3(2H)-one; pyroquilon, proquinazid, 6-iodo-2-propoxy-3-propylquinazolin-4(3H)-one (WO 97/48684); PF 56951 8 tricyclazole, 5-methyl-1,2,4-triazolo[3,4-^benzothiazole (GB 14 19 121); acibenzolar-S-methyl, methyl benzo[1,2,3]thiadiazole-7-carbothionate; captafol, N-(1,1,2,2-tetrachloroethylthio)cyclohex-4-ene-1,2-dicarboximide; captan, 2-trichloromethylsulfanyl-3a,4,7,7a-tetrahydroisoindole-1,3-dione (US 2 553 770); dazomet, 3,5-dimethyl-1,3,5-thiadiazinane-2-thione; folpet, 2-trichloromethylsulfanylisoindole-1,3-dione (US 2 553 770); fenoxanil, N-(1-cyano-1,2-dimethylpropyl)-2-(2,4-dichlorophenoxy) propanamide; quinoxyfen, 5,7-dichloro-4-(4-fluorophenoxy)quinoline (US 5 240 940); mancozeb, manganese ethylenebis(dithiocarbanate) zinc complex (US 3 379 610); maneb, manganese ethylenebis(dithiocarbamate) (US 2 504 404); metam, methyldithiocarbaminic acid (US 2 791 605); metiram, zinc ammoniate ethylenebis(dithiocarbamate) (US 3 248 400); propineb, zinc propylenebis(dithiocarbamate) polymer (BE 611 960); ferbam, iron(3+) dimethyldithiocarbamate (US 1 972 961); thiram, bis(dimethylthiocarbamoyl) disulfide (DE 642 532); ziram, dimethyldithiocarbamate; zineb, zinc ethylenebis(dithiocarbamate) (US 2 457 674); diethofencarb, isopropyl 3,4-diethoxycarbanilate; iprovalicarb, isopropyl [(1S)-2-methyl-1 -(1-p-tolylethylcarbamoyl)propyl]carbamate (EP-A 472 996); flubenthiavalicarb (benthiavalicarb), isopropyl {(S)-1-[(1R)-1-(6-fluorobenzothiazol-2-yl)- ethylcarbamoyl]-2-methylpropyl}carbamate (JP-A 09/323 984); propamocarb, propyl 3-(dimethylamino)propylcarbamate (DE 16 43 040); dodine, (2,4-dichlorophenoxy)acetic acid (US 2 867 562); iminoctadine, bis(8-guanidinooctyl)amine (GB 11 14 155); guazatine, mixture of products from the amidation of irninodi(octamethylene)diamine, mainly iminoctadine; kasugamycin, 1L-1,3,4/2,5,6-1-deoxy-2,3,4,5,6-pentahydroxycyclohexyl 2-amino- 2,3,4,6-tetradeoxy-4-(α-iminoglycino)-α-D-arabino-hexopyranoside; streptomycin, O-2-deoxy-2-methylamino-a-L-glucopyranosyl-(1→2)-O-5-deoxy-3-C- formyl-a-L-lyxofuranosyl-(1→4)N1,N3-diamidino-D-streptamine; polyoxins, 5-(2-amino-5-O-carbamoy!-2-deoxy-L-xylonamido)-1-(5-carboxy-1,2,3,4- tetrahydro-2,4-dioxopyrimidin-1-yl)-1,5-dideoxy-β-D-allofuranuronic acid and the salts thereof; validamycin A, binapacryl, (RS)-2-sec-butyl-4,6-dinitrophenyl 3-methylcrotonate; dinocap, the mixture of 2,6-dinitro-4-octylphenyl crotonate and 2,4-dinitro-6-octylphenyl crotonate, wherein "octyl" is a mixture of 1-methylheptyl, 1-ethylhexyl and 1-propylpentyl (US 2 526 660); dinobuton, (RS)-2-sec-butyl-4,6-dinitrophenyl isopropyl carbonate; dithianon, 5,10-dioxo-5,10-dihydronaphtho[2,3-b][1,4]dithiin-2,3-dicarbonitrile PF 56951 9 (GB 857 383); isoprothiolane, indol-3-ylacetic acid; fentin acetate, triphenyltin acetate (US 3 499 086); edifenphos, O-ethyl S,S-diphenyl phosphorodithioate; iprobenfos, S-benzyl O,O-diisopropyl phosphorothioate (Jpn. Pesticide Inf., No. 2, S. 11 (1970)); fosetyl, fosetyl-aluminum, (aluminum) ethylphosphonate (FR 22 54 276); pyrazophos, ethyl 2-diethoxyphosphinothioyloxy-5-methylpyrazolo[1,5-a]pyrimidine-6- carboxylate (DE 15 45 790); tolclofos-methyl, O-2,6-dichloro-p-tolyl O,O-dimethyl phosphorothioate (GB 14 67 561); chlorothalonil, 2,4,5,6-tetrachloroisophthalonitrile (US 3 290 353); dichlofluanid, N-dichlorofluoromethylthio-N,N-dimethyl-N-phenylsulfamide (DE 11 93 498); flusulfamide, 2',4-dichloro-α,α,α-trifluoro-4'-nitro-m-toluenesulfanilide (EP-A 199 433); hexachlorobenzene (C. R. Seances Acad. Agric. Fr, Vol. 31, p. 24 (1945)); phthalide(DE16 43 347); pencycuron, 1-(4-chlorobenzyl)-1-cyclopentyl-3-phenylurea (DE 27 32 257); quintozene, pentachloronitrobenzene (DE 682 048); thiophanate-methyl, 1,2-phenylenebis(iminocarbonothioyl)bis(dimethylcarbamate) (DE-OS 19 30 540); tolylfluanid, N-dichlorofluoromethylthio-N,N-dimethyl-N-p-tolylsulfamide (DE 11 93 498); Bordeaux mixture, mixture of calcium hydroxide and copper(ll) sulfate; copper hydroxide, Cu(OH)2; copper oxychloride, Cu2CI(OH)3; cyflufenamid, (Z)-N-[α-(cyclopropylmethoxyimino)-2,3-difluoro-6-(trifluoromethyl)ben- zyl]-2-phenylacetamide (WO 96/19442); cymoxanil, 1-(2-cyano-2-methoxyiminoacetyl)-3-ethylurea (US 3 957 847); dimethirimol, 5-butyl-2-dimethylamino-6-methylpyrimidin-4-ol (GB 11 82 584); ethirimol, 5-butyl-2-ethylamino-6-methylpyrimidin-4-ol (GB 11 82 584); furalaxyl, methyl N-(2-furoyl)-N-(2,6-xylyl)-DL-alaninate (GB 14 48 810); metrafenone, 3'-bromo-2,3,4,6'-tetramethoxy-2',6-dimethylbenzophenone (US 5 945 567); spiroxamine, (8-tert-butyl-1,4-dioxaspiro[4.5]dec-2-yl)diethylamine (EP-A 281 842). The compounds named according to IUPAC, their preparation and their fungicidal action are likewise known: methyl (2-chloro-5-[1-(3-methylbenzyloxyimino)ethyl]benzyl)carbamate, methyl (2- chloro-5-[1-(6-methylpyridin-2-ylmethoxyimino)ethyl]benzyl)carbamate (EP-A 12 01 648); methyl 2-(ortho-((2,5-dimethylphenyloxymethylene)phenyl)-3-methoxyacrylate (EP-A 226 917); 5-chloro-7-(4-methylpiperidin-1 -yl)-6-(2,4,6-trifluorophenyl)-[1,2,4]triazolo[1,5-a]pyri- midine (WO 98/46608), PF 56951 10 3,4-dichloro-N-(2-cyanophenyl)isothiazole-5-carboxamide (WO 99/24413), N-(2-{4-[3-(4-chlorophenyl)prop-2-ynyloxy]-3-methoxyphenyl}ethyl)-2-methanesulfonyl- amino-3-methylbutyramide, N-(2-{4-[3-(4-chlorophenyl)prop-2-ynyloxy]-3-methoxyphe- nyl}ethyl)-2-ethanesulfonylamino-3-methylbutyramide (WO 04/049804), N-(4'-bromobiphenyl-2-yl)-4-difluoromethyl-2-methylthiazole-5-carboxamide, N-(4'- trifluoromethylbiphenyl-2-yl)-4-difluoromethyl-2-methylthiazole-5-carboxamide, N-(4'- chloro-3'-fluorobiphenyl-2-yl)-4-difluoromethyl-2-methylthiazole-5-carboxamide, N- (3',4'-dichloro-4-fluorobiphenyl-2-yl)-3-difluoromethyl-1-methylpyrazole-4-carboxamide (WO 03/066609), N-(3',4'-dichloro-5-fluorobiphenyl-2-yl)-3-difluoromethyl-1- methylpyrazole-4-carboxamide (WO 03/053145); 2-butoxy-6-iodo-3-propylchromen-4-one (WO 03/14103), 3-[5-(4-chlorophenyl)-2,3-dimethylisoxazolidin-3-yl]pyridine (EP-A 10 35 122); amisulbrom, N,N-dimethyl-3-(3-bromo-6-fluoro-2-methylindole-1-sulfonyl)- [1,2,4]triazole-1-sulfonamide (WO 03/053145), methyl 3-(4-chlorophenyl)-3-(2-isopropoxycarbonylamino-3-methylbutyrylamino)- propanoate (EP-A 1028125). It is an object of the present invention, with a view to reducing the application rates and broadening the activity spectrum of the known compounds, to provide mixtures which, at a reduced total amount of active compounds applied, have improved activity against harmful fungi, in particular for certain indications. We have found that this object is achieved by the mixtures defined at the outset. Moreover, we have found that simultaneous, that is joint or separate, application of the compounds I and an active compound II or successive application of the compounds I and an active compound II allows better control of harmful fungi than is possible with the individual compounds (synergistic mixtures). The compounds I can be used as a synergist for a large number of different active compounds. The simultaneous, that is joint or separate, application of the compound I with an active compound II increases the fungicidal activity in a superadditive manner. The mixtures of the compounds I and an active compound II or the simultaneous, that is joint or separate, use of the compounds I and an active compound II are/is distinguished by excellent activity against a broad spectrum of phytopathogenic fungi, in particular from the classes of the Ascomycetes, Deuteromycetes, Oomycetes and Basidiomycetes. Some of them are systemically active and can be used in crop protection as foliar fungicides, as fungicides for seed dressing and as soil fungicides. They are particularly important in the control of a multitude of fungi on various crop plants, such as bananas, cotton, vegetables (for example cucumbers, beans and cucurbits), barley, grass, oats, coffee, potatoes, corn, fruit, rice, rye, soybeans, tomatoes, grape vines, wheat, ornamental plants, sugar cane and a multiplicity of PF 56951 11 seeds. Advantageously, they are suitable for controlling the following plant diseases: • Alternaria species on vegetables, oilseed rape, sugar beet and fruit and rice, such as, for example, A. solam'or A. alternata on potatoes and tomatoes; • Aphanomyces species on sugar beet and vegetables; • Ascochyta species on cereals and vegetables; • Bipolaris and Drechslera species on corn, cereals, rice and lawns, such as, for example, D. maydis on corn; • Blumeria graminis (powdery mildew) on cereals; • Botrytis cinerea (gray mold) on strawberries, vegetables, flowers and grapevines; • Bremia lactucae on lettuce; • Cercospora species on corn, soybeans, rice and sugar beet; • Cochliobolus species on corn, cereals, rice, such as, for example, Cochliobolus sativus on cereals, Cochliobolus miyabeanus on rice; • Colletotricum species on soybeans and cotton; • Drechslera species, Pyrenophora species on corn, cereals, rice and lawns, such as, for example, D. teres on barley or D. tritici-repentis on wheat; • Esca on grapevines, caused by Phaeoacremonium chlamydosporium, Ph. Aleophilum and Formitipora punctata (syn. Phellinus punctatus), • Exserohilum species on corn; • Erysiphe cichoracearum and Sphaerotheca fuliginea on cucumbers; • Fusarium and Verticillium species on various plants, such as, for example, F. graminearum or F. culmorum on cereals or F. oxysporum on a multitude of plants, such as, for example, tomatoes; • Gaeumanomyces graminis on cereals; • Gibberella species on cereals and rice (for example Gibberella fujikuroi on rice); • Grainstaining complex on rice; • Helminthospohum species on corn and rice; • Michrodochium nivale on cereals; • Mycosphaerella species on cereals, bananas and groundnuts, such as, for example, M. graminicola on wheat or M.fijiensis on bananas; • Peronospora species on cabbage and bulbous plants, such as, for example, P. brassicae on cabbage or P. destructor on onions; • Phakopsara pachyrhizi and Phakopsara meibomiae on soybeans; • Phomopsis species on soybeans and sunflowers; • Phytophthora infestans on potatoes and tomatoes; • Phytophthora species on various plants, such as, for example, P. capsici on bell pepper; • Plasmopara viticola on grapevines; • Podosphaera leucotricha on apples; PF 56951 12 • Pseudocercosporella herpotrichoides on cereals; • Pseudoperonospora on various plants, such as, for example, P. cubensis on cucumber or P. humillion hops; • Puccinia species on various plants, such as, for example, P. triticina, P. striformins, P. horde/or P.graminis on cereals or P. asparagi on asparagus; • Pyricularia oryzae, Corticium sasakii, Sarocladium oryzae, S.attenuatum, Entyloma oryzae on rice; • Pyricularia grisea on lawns and cereals; • Pythium spp. on lawns, rice, com, cotton, oilseed rape, sunflowers, sugar beet, vegetables and other plants, such as, for example, P. ultiumum on various plants, P. aphanidermatum on lawns; • Rhizoctonia species on cotton, rice, potatoes, lawns, corn, oilseed rape, potatoes, sugar beet, vegetables and on various plants, such as, for example, R. solani on beet and various plants; • Rhynchosporium secalis on barley, rye and triticale; • Sclerotinia species on oilseed rape and sunflowers; • Septoria tritici and Stagonospora nodorum on wheat; • Erysiphe (syn. Uncinula) necator on grapevines; • Setospaeria species on corn and lawns; • Sphacelotheca reilinia on corn; • Thievaliopsis species on soybeans and cotton; • Tilletia species on cereals; • Ustilago species on cereals, com and sugar cane, such as, for example, U. maydis on corn; • Venturia species (scab) on apples and pears, such as, for example, V. inaequalis on apples. The mixtures of the compounds I and active compounds II are suitable in particular for controlling harmful fungi from the class of the Peronosporomycetes (syn. Oomycetes), such as Peronospora species, Phytophthora species, Plasmopara viticola and Pseudoperonospora species, in particular fungi corresponding to those mentioned above. The compounds I and active compounds II can be applied simultaneously, that is jointly or separately, or in succession, the sequence, in the case of separate application, generally not having any effect on the result of the control measures. In the definitions of the symbols given for the formulae above, collective terms were used which generally represent the following substituents: halogen: fluorine, chlorine, bromine and iodine; PF 56951 13 alkyl: saturated straight-chain or branched hydrocarbon radicals having 1 to 4, 6, 8 or 10 carbon atoms, for example C1-C6-alkyl, such as methyl, ethyl, propyl, 1-methylethyl, butyl, 1-methylpropyl, 2-methylpropyl, 1,1-dimethylethyl, pentyl, 1-methylbutyl, 2-me- thylbutyl, 3-methylbutyl, 2,2-dimethylpropyl, 1-ethylpropyl, hexyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, 1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1,1-dimethylbutyl, 1,2-dimethylbutyl, 1,3-dimethylbutyl, 2,2-dimethylbutyl, 2,3-dime- thylbutyl, 3,3-dimethylbutyl, 1-ethylbutyl, 2-ethylbutyl, 1,1,2-trimethylpropyl, 1,2,2-tri- methylpropyl, 1-ethyl-1-methylpropyl and 1-ethyl-2-methylpropyl; haloalkyl: straight-chain or branched alkyl groups having 1 to 2, 4 or 6 carbon atoms (as mentioned above), where some or all of the hydrogen atoms in these groups may be replaced by halogen atoms as mentioned above: in particular C1-C2-haloalkyl, such as chloromethyl, bromomethyl, dichloromethyl, trichloromethyl, fluoromethyl, difluoromethyl, trifluoromethyl, chlorofluoromethyl, dichlorofluoromethyl, chlorodifluoromethyl, 1-chloroethyl, 1-bromoethyl, 1-fluoroethyl, 2-fluoroethyl, 2,2- difluoroethyl, 2,2,2-trifluoroethyl, 2-chloro-2-fluoroethyl, 2-chloro-2,2-difluoroethyl, 2,2- dichloro-2-fluoroethyl, 2,2,2-trichloroethyl, pentafluoroethyl or 1,1,1 -trifluoroprop-2-yl. With a view to the intended use of the azolopyhmidinylamines of the formula I, particular preference is given to the following meanings of the substituents, in each case on their own or in combination: Particularly suitable for the mixtures according to the invention are compounds of the formula I in which R1 is straight-chain or branched C3-C12-alkyl or phenyl which may be substituted by one to three halogen or C1-C4-alkyl groups. In one embodiment of the compounds of the formula I, group Ra is absent. A preferred embodiment relates to compounds of the formula I in which R1 is straight- chain or branched C5-C10-alkyl, in particular ethyl, 3,5,5-trimethylhexyl, n-heptyl, n- octyl, n-nonyl and n-decyl. A further embodiment relates to the compounds of the formula I in which R1 is phenyl which is unsubstituted or substituted by one to four halogen, cyano, hydroxyl, mercapto, nitro, NRARB, C1-C10-alkyl, C1-C6-haloalkyl, C2-C6-alkenyl, C2-C6-alkynyl and C1-C6-alkoxy groups. Preferred compounds of the formula I are those in which R1 is a substituted phenyl group which corresponds to a group G PF 56951 14 in which L1 is cyano, halogen, hydroxyl, mercapto, nitro, NRARB, C1-C10-alkyl, C1-C6- haloalkyl, C2-C6-alkenyl, C2-C6-alkynyl and C1-C6-alkoxy; and L2,L3 independently of one another are hydrogen or one of the groups mentioned under L1 and # denotes the bond to the azolopyrimidine skeleton. In a further embodiment of the compounds of the formula I, L1 is cyano, halogen, hydroxyl, mercapto, nitro, NRARB, C1-C6-alkyl, halomethyl or C1-C2-alkoxy, preferably cyano, halogen, C1-C6-alkyl, halomethyl or C1-C2-alkoxy. In a further embodiment of the compounds of the formula I, L2 is hydrogen or one of the groups mentioned above. In a further embodiment of the compounds of the formula I, L3 is hydrogen, cyano, halogen, hydroxyl, mercapto, nitro, NRARB, C1-C6-alkyl, halomethyl or C1-C2-alkoxy, preferably hydrogen. Preference is given to compounds of the formula I in which R2 is straight-chain or branched C1-C12-alkyl, C1-C4-alkoxy-C1-C4-alkyl or C1-C4-haloalkyl. In a particularly preferred embodiment of the compounds of the formula I, R2 is methyl, ethyl, n-propyl, n-octyl, trifluoromethyl or methoxymethyl, in particular methyl, ethyl, trifluoromethyl or methoxymethyl. Preference is furthermore given to compounds of the formula I in which R3 is hydrogen. In a further embodiment of the compounds of the formula I, R3 is amino. One embodiment of the compounds of the formula I relates to those in which A'is N. These compounds correspond to the formula IA in which the variables are as defined for formula I: Another embodiment of the compounds of the formula I relates to those in which A is CH. These compounds correspond to the formula IB in which the variables are as PF 56951 15 defined for formula I: In a further embodiment of preferred compounds I, the carbon chains of R1 and R2 together do not have more than 12 carbon atoms. Especially preferred with a view to their use are the compounds I compiled in the tables below. The groups mentioned for a substituent in the tables are furthermore per se, independently of the combination in which they are mentioned, a particularly preferred embodiment of the substituent in question. Table 1 Compounds of the formula IA in which the combination of R1, R2 and R3 for a compound corresponds in each case to one row of Table I Table 2 Compounds of the formula IB in which the combination of R1, R2 and R3 for a compound corresponds in each case to one row of Table I Table I PF 56951 16 PF 56951 17 PF 56951 18 PF 56951 19 PF 56951 20 PF 56951 21 PF 56951 22 PF 56951 23 Preferred embodiments of the mixtures according to the invention comprise, as active component 1, a compound selected from the following list: 6-(3,4-dichlorophenyl)-5-methyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine, 6-(4-tert-butylphenyl)-5-methyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine, 5-methyl-6-(3,5,5-trimethylhexyl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine, 5-methyl-6-octyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine, 5-ethyl-6-octyl-[1,2,4]triazolo[1,5-a]pyrimidine-2,7-diamine, 6-ethyl-5-octyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine, 5-ethyl-6-octyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine, 5-ethyl-6-(3,5,5-trimethylhexyl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine, 6-octyl-5-propyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine, 5-methoxymethyl-6-octyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine, 6-octyl-5-trifluoromethyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine and 5-trifluoromethyl-6-(3,5,5-trimethylhexyl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine. Further preferred embodiments of the mixtures according to the invention relate to combinations of one of the compounds of Table 1, in particular one of the preferred compounds I hereinabove, and one of the following active compounds II: A) azoles, such as cyproconazole, difenoconazole, fluquinconazole, flusilazole, metconazole, propiconazole, prothioconazole, tebuconazole prochloraz, cyazofamid; carbendazim; ethaboxam; B) strobilurins, such as azoxystrobin, enestroburin, fluoxastrobin, pyraclo- strobin, trifloxystrobin or methyl (2-chloro-5-[1-(3-methylbenzyloxyimino)- ethyl]benzyl)carbamate [B-6], methyl (2-chloro-5-[1-(6-methylpyridin-2-yl- methoxyimino)ethyl]benzyl)carbamate [B-7]; C) carboxamides, such as benalaxyl, boscalid, metalaxyl, ofurace, oxadixyl, dimethomorph; fluopicolide (picobenzamid), zoxamide; mandipropamid; D) heterocylic compounds, such as fluazinam; cyprodinil, pyrimethanil; dodemorph, iprodione, vinclozolin; famoxadone, fenamidone; amisulbrom; PF 56951 24 5-chloro-7-(4-methylpiperidin-1-yl)-6-(2,4,6-trifluorophenyl)-[1,2,4]tri- azolo[1,5-a]pyrimidine [D-8], captan, folpet; E) carbamates, such as mancozeb, maneb, metiram, propineb; iprovalicarb, flubenthiavalicarb; methyl 3-(4-chlorophenyl)-3-(2-isopropoxycarbonylamino-3-methyl- butyrylamino)propanoate [E-7]; and F) other active compounds, selected from sulfur-containing heterocyclyl compounds: dithianon; organophosphorus compounds: fosetyl, fosetyl-aluminum, phosphorous acid and its salts; organochlorine compounds: chlorothalonil, thiophanate-methyl; inorganic active compounds: Bordeaux mixture, copper acetate, copper hydroxide, copper oxychloride, basic copper sulfate; others: cymoxanil, metrafenone; growth retardants: prohexadione and its salts. Preferred embodiments relate to the compositions listed in table A, where in each case one row of table A corresponds to a fungicidal composition comprising the particular compound of the formula I mentioned (component 1) and one active compound of the groups mentioned, this active compound preferably being selected from the preferred embodiments defined above. Table A PF 56951 25 PF 56951 26 The active compounds mentioned above can also be employed in the form of their agriculturally compatible salts. These are usually the alkali metal or alkaline earth metal salts, such as sodium, potassium or calcium salts. When preparing the mixtures, preference is given to using the pure active compounds which, if required, may be mixed with further active compounds against harmful fungi or other pests, such as insects, arachnids or nematodes, or else herbicidal or growth- regulating active compounds or fertilizers as further active components. In a preferred embodiment of the invention, mixtures of an azolopyrimidinylamine and an active compound II are used. Under certain conditions, it may be advantageous to combine an azolopyrimidinylamine with two or more active compounds II. In addition, mixtures of two or more compounds I with one or more active compounds II may also be suitable. Suitable further active components in the above sense are in particular the active compounds II, mentioned at the outset, and in particular the preferred active compounds mentioned above. In the case of ternary mixtures, preferred third active components are strobilurins, in particular pyraclostrobin, carboxamides, in particular boscalid, and also organophosphorus compounds, in particular phosphorous acid and its salts. The compounds I and active compounds II are usually employed in a weight ratio of PF 56951 27 from 100:1 to 1:100, preferably from 50:1 to 1:50, preferably from 20:1 to 1:20, in particular from 10:1 to 1:10. The further active components are, if desired, added in a ratio of from 50:1 to 1:50, preferably from 20:1 to 1:20, to the compound I. Depending on the type of compound and the desired effect, the application rates of the mixtures according to the invention are from 5 g/ha to 2000 g/ha, preferably from 50 to 900 g/ha, in particular from 50 to 750 g/ha. Correspondingly, the application rates for compounds I are generally from 1 to 1000 g/ha, preferably from 10 to 900 g/ha, in particular from 20 to 750 g/ha. Depending on the type of active compound II, the application rates for active compounds II are generally from 1 to 2000 g/ha, preferably from 10 to 900 g/ha, in particular from 40 to 500 g/ha. In the treatment of seed, for example by dusting, coating or soaking seeds, application rates of mixture are generally from 1 to 1000 g/100 kg of seed, preferably from 1 to 750 g/100 kg, in particular from 5 to 500 g/100 kg. The method for controlling harmful fungi is carried out by the separate or joint application of the compounds I and active compounds II or the mixtures of compounds I and active compounds II by spraying or dusting the seeds, the plants or the soils before or after sowing of the plants or before or after emergence of the plants. The mixtures according to the invention, or the compounds I and active compounds II can be converted into the customary formulations, for example solutions, emulsions, suspensions, dusts, powders, pastes and granules. The use form depends on the particular intended purpose; in each case, it should ensure a fine and even distribution of the compound according to the invention. The formulations are prepared in a known manner, for example by extending the active compound with solvents and/or carriers, if desired using emulsifiers and dispersants. Solvents/auxiliaries suitable for this purpose are essentially: water, aromatic solvents (for example Solvesso products, xylene), paraffins (for example mineral oil fractions), alcohols (for example methanol, butanol, pentanol, benzyl alcohol), ketones (for example cyclohexanone, gamma-butyrolactone), pyrrolidones (NMP, NOP), acetates (glycol diacetate), glycols, fatty acid dimethylamides, fatty acids and fatty acid esters. In principle, solvent mixtures may also be used, carriers such as ground natural minerals (for example kaolins, clays, talc, chalk) PF 56951 28 and ground synthetic minerals (for example highly disperse silica, silicates); emulsifiers such as nonionogenic and anionic emulsifiers (for example polyoxyethylene fatty alcohol ethers, alkylsulfonates and arylsulfonates) and dispersants such as lignosulfite waste liquors and methylcellulose. Suitable surfactants used are alkali metal, alkaline earth metal and ammonium salts of lignosulfonic acid, naphthalenesulfonic acid, phenolsulfonic acid, dibutylnaphthalenesulfonic acid, alkylarylsulfonates, alkyl sulfates, alkylsulfonates, fatty alcohol sulfates, fatty acids and sulfated fatty alcohol glycol ethers, furthermore condensates of sulfonated naphthalene and naphthalene derivatives with formaldehyde, condensates of naphthalene or of naphthalenesulfonic acid with phenol and formaldehyde, polyoxyethylene octylphenyl ether, ethoxylated isooctylphenol, octylphenol, nonylphenol, alkylphenyl polyglycol ethers, tributylphenyl polyglycol ether, tristearylphenyl polyglycol ether, alkylaryl polyether alcohols, alcohol and fatty alcohol ethylene oxide condensates, ethoxylated castor oil, polyoxyethylene alkyl ethers, ethoxylated polyoxypropylene, lauryl alcohol polyglycol ether acetal, sorbitol esters, lignosulfite waste liquors and methylcellulose. Substances which are suitable for the preparation of directly sprayable solutions, emulsions, pastes or oil dispersions are mineral oil fractions of medium to high boiling point, such as kerosene or diesel oil, furthermore coal tar oils and oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons, for example toluene, xylene, paraffin, tetrahydronaphthalene, alkylated naphthalenes or their derivatives, methanol, ethanol, propanol, butanol, cyclohexanol, cyclohexanone, isophorone, highly polar solvents, for example dimethyl sulfoxide, N-methylpyrrolidone and water. Powders, materials for spreading and dustable products can be prepared by mixing or concomitantly grinding the active substances with a solid carrier. Granules, for example coated granules, impregnated granules and homogeneous granules, can be prepared by binding the active compounds to solid carriers. Examples of solid carriers are mineral earths such as silica gels, silicates, talc, kaolin, attaclay, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium sulfate. magnesium sulfate, magnesium oxide, ground synthetic materials, fertilizers, such as, for example, ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas, and products of vegetable origin, such as cereal meal, tree bark meal, wood meal and nutshell meal, cellulose powders and other solid carriers. Formulations for the treatment of seed may additionally comprise binders and/or gelling agents and, if appropriate, colorants. In general, the formulations comprise from 0.01 to 95% by weight, preferably from 0.1 PF 56951 29 to 90% by weight, of the active compounds. The active compounds are employed in a purity of from 90% to 100%, preferably 95% to 100%. For the treatment of seed, the formulations in question give, after two-to-tenfold dilution, active compound concentrations of from 0.01 to 60% by weight, preferably from 0.1 to 40% by weight, in the ready-to-use preparations. The following are examples of formulations according to the invention: 1. Products for dilution with water A Water-soluble concentrates (SL, LS) 10 parts by weight of a mixture according to the invention are dissolved in 90 parts by weight of water or in a water-soluble solvent. As an alternative, wetters or other auxiliaries are added. The active compound dissolves upon dilution with water. In this way, a formulation having a content of 10% by weight of active compound is obtained. B Dispersible concentrates (DC) 20 parts by weight of a mixture according to the invention are dissolved in 70 parts by weight of cyclohexanone with addition of 10 parts by weight of a dispersant, for example polyvinylpyrrolidone. Dilution with water gives a dispersion. The active compound content is 20% by weight. C Emulsifiable concentrates (EC) 15 parts by weight of a mixture according to the invention are dissolved in 75 parts by weight of xylene with addition of calcium dodecylbenzenesulfonate and castor oil ethoxylate (in each case 5 parts by weight). Dilution with water gives an emulsion. The formulation has an active compound content of 15% by weight. D Emulsions (EW, EO, ES) 25 parts by weight of a mixture according to the invention are dissolved in 35 parts by weight of xylene with addition of calcium dodecylbenzenesulfonate and castor oil ethoxylate (in each case 5 parts by weight). This mixture is introduced into 30 parts by weight of water by means of an emulsifying machine (Ultraturrax) and made into a homogeneous emulsion. Dilution with water gives an emulsion. The formulation has an active compound content of 25% by weight. E Suspensions (SC, OD, FS) In an agitated ball mill, 20 parts by weight of a mixture according to the invention are comminuted with addition of 10 parts by weight of dispersants and wetters and 70 parts by weight of water or an organic solvent to give a fine active compound suspension. Dilution with water gives a stable suspension of the active compound. The active compound content in the formulation is 20% by weight. PF 56951 30 F Water-dispersible granules and water-soluble granules (WG, SG) 50 parts by weight of a mixture according to the invention are ground finely with addition of 50 parts by weight of dispersants and wetters and prepared as water- dispersible or water-soluble granules by means of technical appliances (for example extrusion, spray tower, fluidized bed). Dilution with water gives a stable dispersion or solution of the active compound. The formulation has an active compound content of 50% by weight. G Water-dispersible powders and water-soluble powders (WP, SP, SS, WS) 75 parts by weight of a mixture according to the invention are ground in a rotor-stator mill with addition of 25 parts by weight of dispersants, wetters and silica gel. Dilution with water gives a stable dispersion or solution of the active compound. The active compound content of the formulation is 75% by weight. H Gel formulations In a ball mill, 20 parts by weight of a mixture according to the invention, 10 parts by weight of dispersant, 1 part by weight of gelling agent and 70 parts by weight of water or an organic solvent are ground to give a fine suspension. On dilution with water, a stable suspension having an active compound content of 20% by weight is obtained. 2. Products to be applied undiluted I Dustable powders (DP, DS) 5 parts by weight of a mixture according to the invention are ground finely and mixed intimately with 95 parts by weight of finely divided kaolin. This gives a dustable product having an active compound content of 5% by weight. J Granules (GR, FG, GG, MG) 0.5 part by weight of a mixture according to the invention is ground finely and associated with 99.5 parts by weight of carriers. Current methods are extrusion, spray- drying or the fluidized bed. This gives granules to be applied undiluted having an active compound content of 0.5% by weight. K ULV solutions (UL) 10 parts by weight of a mixture according to the invention are dissolved in 90 parts by weight of an organic solvent, for example xylene. This gives a product to be applied undiluted having an active compound content of 10% by weight. For seed treatment, use is usually made of water-soluble concentrates (LS), suspensions (FS), dustable powders (DS), water-dispersible and water-soluble powders (WS, SS), emulsions (ES), emulsifiable concentrates (EC) and gel PF 56951 31 formulations (GF). These formulations can be applied to the seed in undiluted form or, preferably, diluted. Application can be carried out prior to sowing. Preference is given to using FS formulations for seed treatment. Usually, such formulations comprise from 1 to 800 g of active compound/I, from 1 to 200 g of surfactants/I, from 0 to 200 g of antifreeze agents/I, from 0 to 400 g of binder/I, from 0 to 200 g of colorants/I and solvents, preferably water. Analogous formulations A to K of the compounds I or an active compound II comprise the respective amount of the individual active compounds. They are usually mixed directly prior to application during dilution to the ready-to-use active compound concentration (tank mix). The active compound concentrations in the ready-to-use preparations may be varied within relatively wide ranges. In general, they are between 0.0001 and 10%, preferably between 0.01 and 1%. The active compounds can be used as such, in the form of their formulations or the use forms prepared therefrom, for example in the form of directly sprayable solutions, powders, suspensions or dispersions, emulsions, oil dispersions, pastes, dustable products, materials for spreading, or granules, by means of spraying, atomizing, dusting, spreading or pouring. The use forms depend entirely on the intended purposes; they are intended to ensure in each case the finest possible distribution of the active compounds according to the invention. Aqueous use forms can be prepared from emulsion concentrates, pastes or wettable powders (wettable powders, oil dispersions) by adding water. To prepare emulsions, pastes or oil dispersions, the substances, as such or dissolved in an oil or solvent, can be homogenized in water by means of a wetter, tackifier, dispersant or emulsifier. However, it is also possible to prepare concentrates composed of active substance, wetter, tackifier, dispersant or emulsifier and, if appropriate, solvent or oil, and such concentrates are suitable for dilution with water. The active compounds may also be used successfully in the ultra-low-volume process (ULV), it being possible to apply formulations comprising over 95% by weight of active compound, or even to apply the active compound without additives. Oils of various types, wetters, adjuvants, herbicides, fungicides, other pesticides, or bactericides may be added to the active compounds, even, if appropriate, not until immediately prior to use (tank mix). These agents may be admixed with the compositions according to the invention in a weight ratio of from 1:100 to 100:1, preferably from 1:10 to 10:1. PF 56951 32 Suitable adjuvants in this sense are in particular: organically modified polysiloxanes, for example Break Thru S 240®; alcohol alkoxylates, for example Atplus 245®, Atplus MBA 1303®, Plurafac LF 300® and Lutensol ON 30®; EO/PO block polymers, for example Pluronic RPE 2035® and Genapol B®; alcohol ethoxylates, for example Lutensol XP 80®; and sodium dioctylsulfosuccinate, for example Leophen RA®. The compounds I and II or the mixtures or the corresponding formulations are applied by treating the harmful fungi, the plants, seeds, soils, areas, materials or spaces to be kept free from them with a fungicidally effective amount of the mixture or, in the case of separate application, of the compounds I and II. Application can be carried out before or after infection by the harmful fungi. Use examples The fungicidal effect of the compounds and the mixtures was demonstrated by the following tests: The active compounds amisulbrom, Cu hydroxide, famoxadone, phosphorous acid and zoxamide were used as commercial formulations and diluted with water to the stated concentrations. The active compounds were separately or jointly prepared as a stock solution comprising 25 mg of active compound which was made up to 10 ml using a mixture of acetone and/or DMSO and the emulsifier Uniperol® EL (wetting agent having emulsifying and dispersing action based on ethoxylated alkylphenols) in a volume ratio of solvent/emulsifier of 99 to 1. The mixture was then made up with water to 100 ml. This stock solution was diluted with the solvent/emulsifier/water mixture described to the concentration of active compound stated below. Use example 1 - Persistency against late blight on tomatoes caused by Phytophthora infestans Leaves of potted plants of the cultivar "Great beef tomato St. Pierre" were sprayed to runoff point with an aqueous suspension having the concentration of active compound stated below. After 5 days, the leaves were inoculated with an aqueous spore suspension of Phytophthora infestans. The plants were then placed in a water vapor-saturated chamber at temperatures between 18 and 20°C. After 6 days, the late blight on the untreated but infected control plants had developed to such an extent that the infection could be determined visually in %. The visually determined percentages of infected leaf areas were converted into PF 56951 33 efficacies in % of the untreated control: The efficacy (E) is calculated as follows using Abbot's formula: E = (1-α/β).100 α corresponds to the fungicidal infection of the treated plants in % and β corresponds to the fungicidal infection of the untreated (control) plants in % An efficacy of 0 means that the infection level of the treated plants corresponds to that of the untreated control plants; an efficacy of 100 means that the treated plants were not infected. The expected efficacies of active compound combinations were determined using Colby's formula (Colby, S.R. "Calculating synergistic and antagonistic responses of herbicide combinations", Weeds, 15, 20-22, 1967) and compared with the observed efficacies. Colby's formula: E = x + y-x. y/100 E expected efficacy, expressed in % of the untreated control, when using the mixture of the active compounds A and B at the concentrations a and b x efficacy, expressed in % of the untreated control, when using the active compound A at the concentration a y efficacy, expressed in % of the untreated control, when using the active compound B at the concentration b Table A - Individual active compounds PF 56951 34 PF 56951 35 *) efficacy calculated using Colbys formula Use example 2 - Activity against late blight on tomatoes caused by Phytophthora infestans, protective treatment Leaves of potted tomato plants were sprayed to runoff point with an aqueous suspension PF 56951 36 having the active compound concentration stated below. After seven days, the leaves were infected with an aqueous sporangia suspension of Phytophthora infestans. The plants were then placed in a water vapor-saturated chamber at temperatures between 18 and 20°C. After 6 days, the late blight on the untreated but infected control plants had developed to such an extent that the infection could be determined visually in %. Evaluation was carried out analogously to example 1. Use example 3 - Activity against peronospora of grapevines caused by Plasmopara viticola Leaves of potted grapevines were sprayed to runoff point with an aqueous suspension having the active compound concentration stated below. After three days, the undersides of the leaves were inoculated with an aqueous sporangia suspension of Plasmopara viticola. The vines were then initially placed in a water vapor-saturated chamber at 24°C for 24 hours and then in a greenhouse at temperatures between 20 and 30°C for 5 days. After this time, the plants were again placed in a humid chamber for 16 hours to promote sporangiophore eruption. The extent of the development of the infection on the undersides of the leaves was then determined visually. Evaluation was carried out analogously to example 1. PF 56951 37 Use example 4 - Activity against peronospora of grapevines caused by Plasmopara viticola Leaves of potted grapevines were sprayed to runoff point with an aqueous suspension having the active compound concentration stated below. After seven days, the undersides of the leaves were inoculated with an aqueous sporangia suspension of Plasmopara viticola. The vines were then initially placed in a water vapor-saturated chamber at 24°C for 24 hours and then in a greenhouse at temperatures between 20 and 30°C for 5 days. After this time, the plants were again placed in a humid chamber for 16 hours to promote sporangiophore eruption. The extent of the development of the infection on the undersides of the leaves was then determined visually. Evaluation was carried out analogously to example 1. PF 56951 38 Microtests The active compounds were formulated separately as a stock solution of a concentration of 10 000 ppm in DMSO. The active compounds fluazinam, pyraclostrobin, copper hydroxide, flubenthiavalicarb, phosphorous acid, dodemorph, zoxamide, amidosulbrom and trifloxystrobin were used as commercial formulations and diluted with water to the stated concentrations. Use example 5 - Activity against the late blight pathogen Phytophthora infestans in the microtiter test The stock solution is pipetted onto a microtiter plate (MTP) and diluted to the stated active compound concentration using a pea juice-based aqueous nutrient medium for fungi. An aqueous zoospore suspension of Phytophthora infestans was then added. The plates were placed in a water vapor-saturated chamber at temperatures of 18°C. Using an absorption photometer, the MTPs were measured at 405 nm on day 7 after the inoculation. The measured parameters were compared to the growth of the active compound-free control variant and the fungus- and active compound-free blank value to determine the relative growth in % of the pathogens in the individual active compounds. PF 56951 39 PF 56951 40 PF 56951 41 PF 56951 42 PF 56951 43 PF 56951 44 PF 56951 45 Use example 6 - Activity against the gray mold pathogen Botrytis cinerea in the microtiter test The stock solution is pipetted onto a microtiter plate (MTP) and diluted to the stated active compound concentration using a malt-based aqueous nutrient medium for fungi. An aqueous spore suspension of Botrytis cinerea was then added. The plates were placed in a water vapor-saturated chamber at temperatures of 18°C. Using an absorption photometer, the MTPs were measured at 405 nm on day 7 after the inoculation. Evaluation was carried out analogously to example 5. PF 56951 46 PF 56951 47 Use example 7 - Activity against the rice blast pathogen Pyricularia oryzae in the microtiter test The stock solutions were mixed according to the ratio, pipetted onto a microtiter plate (MTP) and diluted to the stated active compound concentration using a malt-based aqueous nutrient medium for fungi. An aqueous spore suspension of Pyricularia oryzae was then added. The plates were placed in a water vapor-saturated chamber at temperatures of 18°C. Using an absorption photometer, the MTPs were measured at 405 nm on day 7 after the inoculation. Evaluation was carried out analogously to example 5. PF 56951 48 PF 56951 49 Use example 8 - Activity against the speckled leaf blotch pathogen Septoria tritici in the microtiter test The stock solution was mixed according to the ratio, pipetted onto a microtiter plate (MTP) and diluted to the stated active compound concentration using a malt-based aqueous nutrient medium for fungi. An aqueous spore suspension of Septoria tritici was then added. The plates were placed in a water vapor-saturated chamber at temperatures of 18°C. Using an absorption photometer, the MTPs were measured at 405 nm on day 7 after the inoculation. Evaluation was carried out analogously to example 5. The test results show that, by virtue of the synergism, the mixtures according to the invention are considerably more effective than had been predicted using Colby's formula. PF 56951 50 Claims 1. A fungicidal mixture comprising, as active components: 1) azolopyrimidinylamines of the formula I, in which the substituents are as defined below: R1 is C3-C12-alkyl, C2-C12-alkenyl, C5-C12-alkoxyalkyl, C3-C6-cycloalkyl, phenyl or phenyl-C1-C4-alkyl; R2 is C1-C12-alkyl, C2-C12-alkenyl, C1-C4-haloalkyl, C1-C4-alkoxy-C1-C4- alkyl; where the aliphatic chains in R1 and/or R2 may be substituted by one to four identical or different groups Ra: Ra is halogen, cyano, hydroxyl, mercapto, C1-C10-alkyl, C1-C10- haloalkyl, C3-C8-cycloalkyl, C2-C10-alkenyl, C2-C10-alkynyl, C1- C6-alkoxy, C1-C6-alkylthio, C1-C6-alkoxy-C1-C6-alkyl or NRARB- RA, RB are hydrogen and C1-C6-alkyl; where the cyclic groups in R1 and/or Ra may be substituted by one to four groups Rb: Rb is halogen, cyano, hydroxyl, mercapto, nitro, NRARB, C1-C10-al- kyl, C1-C6-haloalkyl, C2-C6-alkenyl, C2-C6-alkynyl or C1-C6- alkoxy; R3 is hydrogen, halogen, cyano, NRARB, hydroxyl, mercapto, C1-C6-alkyl, C1-C6-haloalkyl, C3-C8-cycloalkyl, C1-C6-alkoxy, C1-C6-alkylthio, C3- C8-cycloalkoxy, C3-C8-cycloalkylthio, carboxyl, formyl, C1-C10- alkylcarbonyl, C1-C10-alkoxycarbonyl, C2-C10-alkeny!oxycarbonyl, C2- C10-alkynyloxycarbonyl, phenyl, phenoxy, phenylthio, benzyloxy, benzylthio, C1-C6-alkyl-S(O)m-; m is 0, 1 or 2; A is CR3 or N; and 2) at least one active compound II selected from the following groups: PF 56951 51 A) azoles, such as bitertanol, bromuconazole, cyproconazole, difenoconazole, diniconazole, enilconazole, epoxiconazole, fluquinconazole, fenbuconazole, flusilazole, flutriafol, hexaconazole, imibenconazole, ipconazole, metconazole, myclobutanil, penconazole, propiconazole, prothioconazole, simeconazole, triadi- mefon, triadimenol, tebuconazole, tetraconazole, triticonazole; prochloraz, pefurazoate, imazalil, triflumizole, cyazofamid; benomyl, carbendazim, thiabendazole, fuberidazole; ethaboxam, etridiazole, hymexazole; B) strobilurins, such as azoxystrobin, dimoxystrobin, enestroburin, fluoxastrobin, kresoxim-methyl, metominostrobin, orysastrobin, picoxystrobin, pyraclostrobin, trifloxystrobin, or methyl (2-chloro-5-[1- (3-methylbenzyloxyimino)ethyl]benzyl)carbamate, methyl (2-chloro-5- [1-(6-methylpyridin-2-ylmethoxyimino)ethyl]benzyl)carbamate, methyl 2-(ortho-((2,5-dimethylphenyloxymethylene)phenyl)-3-methoxyacryl- ate; C) carboxamides, such as carboxin, benalaxyl, boscalid, fenhexamid, flutolanil, furametpyr, mepronil, metalaxyl, mefenoxam, ofurace, oxadixyl, oxycarboxin, penthiopyrad, thifluzamide, tiadinil, N-(4'-bromobiphenyl- 2-yl)-4-difluoromethyl-2-methylthiazole-5-carboxamide, N-(4'- trifluoromethylbiphenyl-2-yl)-4-difluoromethyl-2-methylthiazole-5- carboxamide, N-(4'-chloro-3'-fluorobiphenyl-2-yl)-4-difluoromethyl-2- methylthiazole-5-carboxamide, N-(3',4'-dichloro-4-fluorobiphenyl-2- yl)-3-difluoromethyl-1 -methylpyrazole-4-carboxamide, N-(3',4'- dichloro-5-fluorobiphenyl-2-yl)-3-difluoromethyl-1-methylpyrazole-4- carboxamide; 3,4-dichloro-N-(2-cyanophenyl)isothiazol-5-carboxamide; dimethomorph, flumorph; fiumetover, fluopicolide (picobenzamid), zoxamide; carpropamid, diclocymet, mandipropamid; N-(2-{4-[3-(4-chlorophenyl)prop-2-ynyloxy]-3-methoxyphenyl}ethyl)-2- methanesulfonylamino-3-methylbutyramide, N-(2-{4-[3-(4- chlorophenyl)-prop-2-ynyloxy]-3-methoxyphenyl}ethyl)-2-ethan- esulfonylamino-3-methyl-butyramide; D) heterocylic compounds, selected from fluazinam, pyrifenox; bupirimate, cyprodinil, fenarimol, ferimzone, mepanipyrim, nuarimol, PF 56951 52 pyrimethanil; triforine; fenpiclonil, fludioxonil; aldimorph, dodemorph, fenpropimorph, tridemorph; fenpropidin, iprodione, procymidone, vinclozolin; famoxadone, fenamidone, octhilinone, probenazole; anilazine, diclomezine, pyroquilon, proquinazid, tricyclazole; amisulbrom; 5-chloro-7-(4-methylpiperidin-1-yl)-6-(2,4,6-trifluorophenyl)-[1,2,4]tri- azolo[1,5-a]pyrimidine, 2-butoxy-6-iodo-3-propylchromen-4-one; acibenzolar-S-methyl, captafol, captan, dazomet, folpet, fenoxanil, quinoxyfen; 3-[5-(4-chlorophenyl)-2,3-dimethylisoxazolidin-3- yl]pyridine; E) carbamates, such as mancozeb, maneb, metam, metiram, ferbam, propineb, thiram, zineb, ziram; diethofencarb, iprovalicarb, flubenthiavalicarb, propamocarb; methyl 3-(4-chlorophenyl)-3-(2-isopropoxycarbonylamino-3-methyl- butyrylamino)propanoate; and F) other active compounds, selected from the group consisting of guanidines: dodine, iminoctadine, guazatine; antibiotics: kasugamycin, streptomycin, polyoxine, validamycin A; nitrophenyl derivates: binapacryl, dinocap, dinobuton; sulfur-containing heterocyclyl compounds: dithianon, isoprothiolane; organometal compounds: fentin salts, such as fentin-acetate; organophosphorus compounds: edifenphos, iprobenfos, fosetyl, fosetyl-aluminum, phosphorous acid and its salts, pyrazophos, tolclofos-methyl; organochlorine compounds: chlorothalonil, dichlofluanid, flusulfamide, hexachlorobenzene, phthalide, pencycuron, quintozene, thiophanate- methyl, tolylfluanid; inorganic active compounds: Bordeaux mixture, copper acetate, copper hydroxide, copper oxychloride, basic copper sulfate, sulfur; others: cyflufenamid, cymoxanil, dimethirimol, ethirimol, furalaxyl, metrafenone and spiroxamine; growth retardants: prohexadione and its salts, trinexapac-ethyl, chlormequat, mepiquat-chloride and diflufenzopyr; in a synergistically effective amount. PF 56951 53 2. The fungicidal mixture according to claim 1, comprising a compound of the formula I and a compound of the formula II in a weight ratio of from 100:1 to 1:100. 3. The fungicidal mixture according to claim 1 or 2, comprising a compound of the formula I corresponding to the formula IA in which R1 is C3-C-12-alkyl, C5-C12-alkoxyalkyl, phenyl or phenyl-C1-C4-alkyl, where phenyl may be substituted by one to three groups Rb; R2 is C1-C12-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy-C1-C4-alkyl; R3 is hydrogen or NH2. 4. The fungicidal mixture according to any of claims 1 to 3, comprising as component 1 a compound selected from the group consisting of 6-(3,4-dichloro- phenyl)-5-methyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine, 6-(4-tert-butylphenyl)- 5-methyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine, 5-methyl-6-(3,5,5-trimethyl- hexyl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine, 5-methyl-6-octyl- [1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine, 6-methyl-5-octyl-[1,2,4]triazolo[1,5- a]pyrimidin-7-ylamine, 6-ethyl-5-octyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine, 5- ethyl-6-octyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine, 5-ethyl-6-(3,5,5-trimethyl- hexyl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine, 6-octyl-5-propyl- [1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine, 5-methoxymethyl-6-octyl- [1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine, 6-octyl-5-trifluormethyl- [1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine and 5-trifluoromethyl-6-(3,5,5~trimethyl- hexyl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine. 5. The fungicida! mixture according to any of claims 1 to 4, comprising as component 2 an active compound II selected from the groups of the azoles, carbamates and carboxamides according to claim 1. 6. The fungicidal mixture according to any of claims 1 to 4, comprising as component 2 an active compound II selected from the groups of the strobilurins, heterocyclic compounds or other active compounds according to claim 1. 7. A ternary fungicidal mixture according to any of claims 1 to 6, comprising two PF 56951 54 active compounds II. 8. A composition, comprising a liquid or solid carrier and a mixture according to any of claims 1 to 7. 9. A method for controlling phytopathogenic harmful fungi, wherein the fungi their habitat or the plants to be protected against fungal attack, the soil or seed are treated with an effective amount of a compound I and at least one compound II according to claim 1. 10. The method according to claim 9, wherein the compounds I and II according to claim 1 are applied simultaneously, that is jointly or separately, or in succession, 11. The method according to claim 9 or 10, wherein the compounds I and II according to claim 1 or the mixture according to any of claims 1 to 4 are/is applied in an amount of from 5 g/ha to 2000 g/ha. 12. The method according to claim 9 or 10, wherein the compounds I and II according to claim 1 or the mixture according to any of claims 1 to 7 are/is applied in an amount of from 1 to 1000 g/100 kg of seed. 13. The method according to any of claims 9 to 12, wherein harmful fungi from the class of the Oomycetes are controlled. 14. Seed, comprising a mixture according to any of claims 1 to 7 in an amount of from 1 to 1000 g/100 kg. 15. A process for preparing a composition according to claim 8 by extending the compounds I and II according to claim 1 with liquid or solid carriers. Fungicidal mixtures comprising, as active components, 1) azolopyrimidinylamines of the formula I, in which the substituents are as defined in the description and 2) at least one active compound II selected from the following groups: azoles, strobilurins, carboxamides, heterocylic compounds, carbamates and other active compounds selected from the group consisting of guanidines, antibiotics, sulfur-containing heterocyclyl compounds, organophosphorus compounds, organochlorine compounds, inorganic active compounds, growth retardants and cyflufenamid, cymoxanil, dimethirimol, ethirimol, furalaxyl, metrafenone and spiroxamine; in a synergistically effective amount. Methods for controlling harmful fungi using mixtures of the compound I with active compounds II and the use of the compound I with active compounds II for preparing such mixtures, and also compositions comprising these mixtures.

Full Text

PF 56951
1
Fungicidal mixtures based on azolopyrimidinylamines
Description
The present invention relates to fungicidal mixtures comprising, as active components,
1) azolopyrimidinylamines of the formula I,

in which the substituents are as defined below:
R1 is C3-C12-alkyl, C2-C12-alkenyl, C5-C12-alkoxyalkyl, C3-C6-cycloalkyl, phenyl
or phenyl-C1-C4-alkyl;
R2 is C1-C12-alkyl, C2-C12-alkenyl, C1-C4-haloalkyl, C1-C4-alkoxy-C1-C4-alkyl;
where the aliphatic chains in R1 and/or R2 may be substituted by one to four
identical or different groups Ra:
Ra is halogen, cyano, hydroxyl, mercapto, C1-C10-alkyl, C1-C10-haloalkyl,
C3-C6-cycloalkyl, C2-C10-alkenyl, C2-C10-alkynyl, C1-C6-alkoxy, C1-C6-
alkylthio, C1-C6-alkoxy-C1-C6-alkyl or NRARB;
RA, RB are hydrogen and C1-C6-alkyl;
where the cyclic groups in R1 and/or Ra may be substituted by one to
four groups Rb:
Rb is halogen, cyano, hydroxyl, mercapto, nitro, NRARB, C1-C10-al-
kyl, C1-C6-haloalkyl, C2-C6-alkenyl, C2-C6-alkynyl or C1-C6-
alkoxy;
R3 is hydrogen, halogen, cyano, NRARB, hydroxyl, mercapto, C1-C6-alkyl, C1-
C6-haloalkyl, C3-C8-cycloalkyl, C1-C6-alkoxy, C1-C6-alkylthio, C3-C8-
cycloalkoxy, C3-C5-cycloalkylthio. carboxyl, formyl, C1-C10-alkylcarbonyl, C1-
C10-alkoxycarbonyl, C2-C10-alkenyloxycarbonyl, C2-C10-alkynyloxycarbonyl,
phenyl, phenoxy, phenylthio, benzyloxy, benzylthio, C1-C6-alkyl-S(O)m-;
m is 0, 1 or 2;
A is CH or N;
and
2) at least one active compound II selected from the following groups:

PF 56951
2
A) azoles, such as bitertanol, bromuconazole, cyproconazole, difenoconazole,
diniconazole, enilconazole, epoxiconazole, fluquinconazole, fenbuconazole,
flusilazole, flutriafol, hexaconazole, imibenconazole, ipconazole,
metconazole, myclobutanil, penconazole, propiconazole, prothioconazole,
simeconazole, triadimefon, triadimenol, tebuconazole, tetraconazole,
triticonazole;
prochloraz, pefurazoate, imazalil, triflumizole, cyazofamid;
benomyl, carbendazim, thiabendazole, fuberidazole;
ethaboxam, etridiazole, hymexazole;
B) strobilurins, such as azoxystrobin, dimoxystrobin, enestroburin, fluoxa-
strobin, kresoxim-methyl, metominostrobin, orysastrobin, picoxystrobin,
pyraclostrobin, trifloxystrobin, or methyl (2-chloro-5-[1-(3-methylbenzyl-
oxyimino)ethyl]benzyl)carbamate, methyl (2-chloro-5-[1-(6-methylpyridin-2-
ylmethoxyimino)ethyl]benzyl)carbamate, methyl 2-(ortho-((2,5-di-
methylphenyloxymethylene)phenyl)-3-methoxyacrylate;
C) carboxamides, such as carboxin, benalaxyl, boscalid, fenhexamid, flutolanil,
furametpyr, mepronil, metalaxyl, mefenoxam, ofurace, oxadixyl,
oxycarboxin, penthiopyrad, thifluzamide, tiadinil, N-(4'-bromobiphenyl-2-yl)-
4-difluoromethyl-2-methylthiazole-5-carboxamide, N-(4'-
trifluoromethylbiphenyl-2-yl)-4-difluoromethyl-2-methylthiazole-5-
carboxamide, N-(4'-chloro-3'-fluorobiphenyl-2-yl)-4-difluoromethyl-2-
methylthiazole-5-carboxamide, N-(3',4'-dichloro-4-fluorobiphenyl-2-yl)-3-
difluoromethyl-1-methylpyrazole-4-carboxamide, N-(3',4'-dichloro-5-
fluorobiphenyl-2-yl)-3-difluoromethyl-1-methylpyrazole-4-carboxamide;
3,4-dichloro-N-(2-cyanophenyl)isothiazol-5-carboxamjde;
dimethomorph, flumorph;
flumetover, fluopicolide (picobenzamid), zoxamide;
carpropamid, diclocymet, mandipropamid;
N-(2-{4-[3-(4-chlorophenyl)prop-2-ynyloxy]-3-methoxyphenyl}ethyl)-2-
methanesulfonylamino-3-methylbutyramide, N-(2-{4-[3-(4-chlorophenyl)-
prop-2-ynyloxy]-3-methoxyphenyl}ethy!)-2-ethanesulfonylamino-3-methyl-
butyramide;
D) heterocylic compounds, such as fluazinam, pyrifenox;
bupirimate, cyprodinil, fenarimol, ferimzone, mepanipyrim, nuarimol,
pyrimethanil;
triforine;
fenpiclonil, fludioxonil;
aldimorph, dodemorph, fenpropimorph, tridemorph; fenpropidin,
iprodione, procymidone, vinclozolin;

PF 56951
3
famoxadone, fenamidone, octhilinone, probenazole;
amisulbrom, anilazine, diclomezine, pyroquilon, proquinazid, tricyclazole;
5-chloro-7-(4-methylpiperidin-1 -yl)-6-(2,4,6-trifluorophenyl)-[1,2,4]tri-
azolo[1,5-a]pyrimidine,
2-butoxy-6-iodo-3-propylchromen-4-one;
acibenzolar-S-methyl, captafol, captan, dazomet, folpet, fenoxanil, quin-
oxyfen; 3-[5-(4-chlorophenyl)-2,3-dimethylisoxazolidin-3-yl]pyridine;
E) carbamates, such as mancozeb, maneb, metam, metiram, ferbam,
propineb, thiram, zineb, ziram;
diethofencarb, iprovalicarb, flubenthiavalicarb, propamocarb;
methyl 3-(4-chlorophenyl)-3-(2-isopropoxycarbonylamino-3-methyl-
butyrylamino)propanoate;
and
F) other active compounds, such as
guanidines: dodine, iminoctadine, guazatine;
antibiotics: kasugamycin, streptomycin, polyoxine, validamycin A;
nitrophenyl derivates: binapacryl, dinocap, dinobuton;
sulfur-containing heterocyclyl compounds: dithianon, isoprothiolane;
organometal compounds: fentin salts, such as fentin-acetate;
organophosphorus compounds: edifenphos, iprobenfos, fosetyl, fosetyl-
aluminum, phosphorous acid and its salts, pyrazophos, tolclofos-methyl;
organochlorine compounds: chlorothalonil, dichlofluanid, flusulfamide,
hexachlorobenzene, phthalide, pencycuron, quintozene, thiophanate-
methyl, tolylfluanid;
inorganic active compounds: Bordeaux mixture, copper acetate, copper
hydroxide, copper oxychloride, basic copper sulfate, sulfur;
others: cyflufenamid, cymoxanil, dimethirimol, ethirimol, furalaxyl,
metrafenone and spiroxamine;
growth retardants: prohexadione and its salts, trinexapac-ethyl,
chlormequat, mepiquat-chloride and diflufenzopyr;
in a synergistically effective amount.
Moreover, the invention relates to a method for controlling harmful fungi using mixtures
of the compound I with active compounds II and to the use of the compound I with
active compounds II for preparing such mixtures, and also to compositions comprising
these mixtures.
The azolopyrimidin-7-ylamines of the formula I referred to above as component 1, their
preparation and their action against harmful fungi are known from the literature (EP-A
71 792; EP-A 141 317; WO 03/009687; WO 05/087771; WO 05/087772; WO

PF 56951
4
05/087773; PCT/EP/05/002426; PCT/EP2006/050922; PCT/EP2006/060399.
The active compounds II mentioned above as component 2, their preparation and their
action against harmful fungi are generally known (cf.:
http://www.hclrss.demon.co.uk/index.html); they are commercially available.
bitertanol, (3-([1,1'-biphenyl]-4-yloxy)-a-(1,1-dimethylethyl)-1 H-1,2,4-triazole-1-ethanol
(DE 23 24 020),
bromuconazole, 1-[[4-bromo-2-(2,4-dichlorophenyl)tetrahydro-2-furanyl]methyl]-1H
1,2,4-triazole (Proc. 1990 Br. Crop. Prot. Conf. - Pests Dis. Vol. 1, p. 459);
cyproconazole, 2-(4-chlorophenyl)-3-cyclopropyl-1 -[1,2,4]triazol-1-ylbutan-2-ol
(US 4 664 696);
difenoconazole, 1-{2-[2-chloro-4-(4-chlorophenoxy)phenyl]-4-methyl-[1,3]dioxolan-2-
ylmethyl}-1H-[1,2,4]triazole (GB-A 2 098 607);
diniconazole, (βE)-β-[(2,4-dichlorophenyl)methylene]-α-(1,1-dimethylethyl)-1H-1,2,4-
triazole-1-ethanol (Noyaku Kagaku, 1983, Vol. 8, p. 575);
enilconazole (imazalil), 1-[2-(2,4-dichlorphenyl)-2-(2-propenyloxy)ethyl]-1H-imidazole
(Fruits, 1973, Vol. 28, p. 545);
epoxiconazole, (2RS,3SR)-1-[3-(2-chlorophenyl)-2,3-epoxy-2-(4-fiuorophenyl)propyl]-
1 H-1,2,4-triazole (EP-A 196 038);
fluquinconazole, 3-(2,4-dichlorophenyl)-6-fiuoro-2-[1,2,4]-triazol-1 -yl-3H-quinazolin-4-
one (Proc. Br. Crop Prot. Conf.-Pests Dis., 5-3, 411 (1992));
fenbuconazole, a-[2-(4-chlorophenyl)ethyl]-a-phenyl-1 H-1,2,4-triazole-1 -propanenitrile
(Proc. 1988 Br. Crop Prot. Conf. - Pests Dis. Vol. 1, p. 33);
flusilazole, 1-{[bis-(4-fluorophenyl)methy!silanyl]methyl}-1H-[1,2,4]triazole (Proc. Br.
Crop Prot. Conf.-Pests Dis., 1, 413 (1984));
flutriafol, α-(2-fluorophenyl)-α-(4-fluorophenyl)-1H-1,2,4-triazole-1-ethanol (EP 15 756);
hexaconazole, 2-(2,4-dichlorophenyl)-1-[1,2,4]triazol-1-ylhexan-2-ol (CAS RN
79983-71-4);
imibenconazole, (4-chlorophenyl)methyl N-(2,4-dichlorophenyl)-1 H-1,2,4-triazole-1 -
ethanimidothioate ((Proc. 1988 Br. Crop Prot. Conf. - Pests Dis. Vol. 2, p. 519),
imidothioate ((Proc. 1988 Br. Crop Prot. Conf. - Pests Dis. Vol. 2, p. 519),
ipconazole, 2-[(4-chlorophenyl)methyl]-5-(1-methylethyl)-1-(1 H-1,2,4-triazol-1-yl-
methyl)cyclopentanol (EP 267 778),
metconazole, 5-(4-chlorobenzyl)-2,2-dimethyl-1 -[1,2,4]triazol-1 -ylmethylcyclopentanol
(GB 857 383);
myclobutanil, 2-(4-chlorophenyl)-2-[1,2,4]triazol-1-ylmethylpentanenitrile (CAS RN
88671-89-0);
penconazole, 1-[2-(2,4-dichlorophenyl)pentyl]-1H-[1,2,4]triazole (Pesticide Manual,
12th Ed. (2000), p.712);
propiconazole, 1-[[2-(2,4-dichlorophenyi)-4-propyl-1,3-dioxolan-2-yl]methyl]-1 H-1,2,4-
triazole (BE 835 579);
prothioconazole, 2-[2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-2,4-

PF 56951
5
dihydro-[1,2,4]triazole-3-thione (WO 96/16048);
simeconazole, α-(4-fluorophenyl)-α-[(trimethylsilyl)methyl]-1H-1,2,4-triazole-1-ethanol
[CAS RN 149508-90-7],
triadimefon, 1-(4-chlorophenoxy)-3,3-dimethyl-1-(1 H-1,2,4-triazol-1-yl)-2-butanone;
triadimenol, β-(4-chlorophenoxy)α-(1,1-dimethylethy)-1H-triazole-1-ethanol;
tebuconazole, 1-(4-chlorophenyl)-4,4-dimethyl-3-[1,2,4]triazol-1-ylmethylpentan-3-ol
(EP-A 40 345);
tetraconazole, 1-[2-(2,4-dichlorophenyl)-3-(1,1,2,2-tetrafluoroethoxy)propyl]-1 H-1,2,4-
triazole (EP 234 242);
triticonazole, (5E)-5-[(4-chlorophenyl)methylene]-2,2-dimethyl-1-(1H-1,2,4-triazol-1-
ylmethyl)cyclopentanol (FR 26 41 277);
prochloraz, N-{propyl-[2-(2,4,6-trichlorophenoxy)ethyl]}imidazole-1 -carboxamide (US
3 991 071);
pefurazoate, 4-pentenyl 2-[(2-furanylmethyl)(1 H-imidazol-1-ylcarbonyl)amino]butanoate
[CAS RN 101903-30-4],
triflumizole, (4-chloro-2-trifluoromethylphenyl)-(2-propoxy-1 -[1,2,4]triazol-1 -ylethyli-
dene)amine (JP-A 79/119 462)
cyazofamid, 4-chloro-2-cyano-N',N-dimethyl-5-(4-methylphenyl)-1 H-imidazole-1 -sulfon-
amide (CAS RN 120116-88-3],
benomyl, N-butyl-2-acetylaminobenzoimidazol-1-carboxamide (US 3 631 176);
carbendazim, methyl (1H-benzoimidazol-2-yl)-carbamate (US 3 657 443);
thiabendazole, 2-(1,3-thiazol-4-yl)benzimidazole (US 3 017 415),
fuberidazole, 2-(2-furanyl)-1H-benzimidazole (DE 12 09 799),
ethaboxam, N-(cyano-2-thienylmethyl)-4-ethyl-2-(ethylamino)-5-thiazolcarboxamide
(EP-A 639 574),
etridiazole,
hymexazole, 5-methyl-1,2-oxazol-3-ol (JP 518249, JP 532202),
azoxystrobin, methyl 2-{2-[6-(2-cyano-1-vinylpenta-1,3-dienyloxy)pyrimidin-4-
yloxy]phenyl}-3-rnethoxyacrylate (EP-A 382 375),
dimoxystrobin, (E)-2-(methoxyimino)-AAmethyl-2-[α-(2,5-xylyloxy)-o-tolyl]acetamide
(EP-A 477 631);
fluoxastrobin, (E)-{2-[6-(2-chlorophenoxy)-5-fluoropyrimidin-4-yIoxy]phenyl}(5,6-
dihydro-1,4,2-dioxazin-3-yl)methanone O-methy!oxime (WO 97/27189);
kresoxim-methyl, methyl (E)-methoxyimino[α-(o-tolyloxy)-o-tolyl]acetate (EP-A
253 213);
metominostrobin, (E)-2-(methoxyimino)-N-methyl-2-(2-phenoxyphenyl)acetamide (EP-
A 398 692);
orysastrobin, (2E)-2-(methoxyimino)-2-{2-[(3E,5E,6E)-5-(methoxyimino)-4,6-dimethyl-
2,8-dioxa-3,7-diazanona-3,6-dien-1-yl]phenyl}-N-methylacetamide (WO 97/15552);
picoxystrobin, methyl 3-methoxy-2-[2-(6-trifluoromethylpyridin-2-yloxymethyl)phenyl]-
acrylate (EP-A 278 595);
pyraclostrobin, methyl N-{2-[1-(4-chlorophenyl)-1H-pyrazol-3-yloxymethyl]phenyl}(N-

PF 56951
6
methoxy)carbamate (WO-A 96/01256);
trifloxystrobin, methyl (E)-methoxyimino-{(E)-α-[1-(α,α,α-trifluoro-m-tolyl)ethylidene-
aminooxy]-o-tolyl}acetate (EP-A 460 575);
carboxin, 5,6-dihydro-2-methyl-N-phenyl-1,4-oxathiin-3-carboxamide (US 3 249 499),
benalaxyl, methyl N-(phenylacetyl)-N-(2,6-xylyl)-DL-alaninate (DE 29 03 612),
boscalid, 2-chloro-N-(4'-chlorbiphenyl-2-yl)nicotinamide (EP-A 545 099);
fenhexamid, N-(2,3-dichloro-4-hydroxyphenyl)-1-methylcyclohexanecarboxamide
(Proc. Br. Crop Prot. Conf. - Pests Dis., 1998, Vol. 2, p. 327);
flutolanil, a,a,a-trifluoro-3'-isopropoxy-otoluanilide (JP 1104514),
furametpyr, 5-chloro-N-(1,3-dihydro-1,1,3-trimethyl-4-isobenzofuranyl)-1,3-dimethyl-1 H-
pyrazole-4-carboxamide [CAS RN 123572-88-3],
mepronil, 3'-isopropoxy-o-toluanilide (US 3 937 840),
metalaxyl, methyl N-(methoxyacetyl)-N-(2,6-xylyl)-DL-alaninate (GB 15 00 581);
mefenoxam, methyl N-(2,6-dimethylphenyl)-N-(methoxyacetyl)-D-alaninate;
ofurace, (RS)-α-(2-chloro-N-2,6-xylylacetamido)-Y-butyrolactone [CAS RN 58810-48-3];
oxadixyl; N-(2,6-dimethylphenyl)-2-methoxy-N-(2-oxo-3-oxazolidinyl)acetamide (GB
20 58 059),
oxycarboxin, 5,6-dihydro-2-methyl-1,4-oxathiin-3-carboxanilide 4,4-dioxide (US
3 399 214),
penthiopyrad, N-[2-(1,3-dimethylbutyl)-3-thienyl]-1-methyl-3-(trifluoromethyl)-1 H-
pyrazole-4-carboxamide (JP 10130268),
thifluzamide, N-[2,6-dibromo-4-(trifluoromethoxy)phenyl]-2-methyl-4-(trifluoromethyl)-5-
thiazolecarboxamide;
tiadinil, 3'-chloro-4,4'-dimethyl-1,2,3-thiadiazole-5-carboxanilide [CAS RN 223580-51-
6],
dimethomorph, 3-(4-chlorophenyl)-3-(3,4-dimethoxyphenyl)-1-morpholin-4-ylpropenone
(EP-A 120 321);
flumorph, 3-(4-fluorophenyl)-3-(3,4-dimethoxyphenyl)-1-morpholin-4-ylpropenone (EP-
A 860 438);
flumetover, 2-(3,4-dimethoxyphenyl)-N-ethyl-a,a,a-trifluoro-N-methyl-p-toluamide
[AGROWNo. 243, 22(1995)],
fluopicolide (picobenzamid), 2,6-dichloro-N-(3-chloro-5-trifluoromethylpyridin-2-
ylmethyl)benzamide (WO 99/42447);
zoxamide, (RS)-3,5-dichloro-N-(3-chloro-1-ethyl-1-methyl-2-oxopropyl)-p-toluamide
[CAS RN 156052-68-5];
carpropamid, 2,2-dichloro-N-[1 -(4-chlorophenyl)ethyl]-1 -ethyl-3-methylcyclopropane-
carboxamide [CAS RN 104030-54-8],
diclocymet, 2-cyano-N-[(1R)-1-(2,4-dichlorophenyl)ethyl]-3,3-dimethyl butanamide;
mandipropamid, (RS)-2-(4-chlorophenyl)-N-[3-methoxy-4-(prop-2-ynyloxy)phenethyl]-2-
(prop-2-ynyloxy)acetamide [CAS RN 374726-62-2];
fluazinam, 3-chloro-N-[3-chloro-2,6-dinitro-4-(trifluoromethyl)phenyl]-5-(trifluoromethyl)-
2-pyridinamine (The Pesticide Manual, publ. The British Crop Protection Council, 10th

PF 56951
7
ed. (1995), p. 474);
pyrifenox, 1-(2,4-dichlorophenyl)-2-(3-pyridinyl)ethanone O-methyloxime (EP-A 49 854);
bupirimate, 5-butyl-2-ethylamino-6-methylpyrimidin-4-yldimethylsulfamate [CAS RN
41483-43-6];
cyprodinil, (4-cyclopropyl-6-methylpyrimidin-2-yl)phenylamine (EP-A 310 550);
fenarimol, (4-chlorophenyl) (2-chlorophenyl) pyrimidin-5-ylmethanol (GB 12 18 623);
ferimzone, (Z)-2'-methylacetophenone 4,6-dimethylpyrimidin-2-ylhydrazone [CAS RN
89269-64-7];
mepanipyrim, (4-methyl-6-prop-1-ynylpyrimidin-2-yl)phenylamine (EP-A 224 339);
nuarimol, α-(2-chlorophenyl)-α-(4-fluorophenyl)-5-pyrimidinemethanol (GB 12 18 623);
pyrimethanil, 4,6-dimethylpyrimidin-2-ylphenylamine (DD-A 151 404);
triforine, N,N-{piperazine-1,4-diylbis[(trichloromethyl)methylene]}diformamide (DE
19 01 421);
fenpiclonil, 4-(2,3-dichlorophenyl)-1H-pyrrole-3-carbonitrile (Proc. 1988 Br. Crop Prot.
Conf. - Pests Dis., Vol. 1, p. 65);
fludioxonil, 4-(2,2-difluorobenzo[1,3]dioxol-4-yl)-1H-pyrrole-3-carbonitrile (The Pesticide
Manual, publ. The British Crop Protection Council, 10th ed. (1995), p. 482);
aldimorph, 4-alkyl-2,5(or 2,6)-dimethylmorpholine, comprising 65-75% of 2,6-dimethyl-
morpholine and 25-35% of 2,5-dimethylmorpholine, comprising more than 85% of 4-
dodecyl-2,5(or 2,6)-dimethylmorpholine, where "alkyl" may also include octyl, decyl,
tetradecyl or hexadecyl and where the cis/trans ratio is 1:1;
dodemorph, 4-cyclododecyl-2,6-dimethylmorpholine (DE 1198125);
fenpropimorph, (RS)-cis-4-[3-(4-tert-butylphenyl)-2-methylpropyl]-2,6-dimethyl-
morpholine (DE 27 52 096);
tridemorph, 2,6-dimethyl-4-tridecylmorpholine (DE 11 64 152);
fenpropidin, (RS)-1-[3-(4-tert-butylphenyl)-2-methylpropyl]piperidine (DE 27 52 096);
iprodione, N-isopropyl-3-(3,5-dichlorophenyl)-2,4-dioxoimidazolidine-1-carboxamide
(GB 13 12 536);
procymidone, N-(3,5-dichlorophenyl)-1,2-dimethylcyclopropane-1,2-dicarboximide (US
3 903 090);
vinclozolin, 3-(3,5-dichlorophenyl)-5-methyl-5-vinyloxazolidine-2,4-dione (DE-OS
22 07 576);
famoxadone, (RS)-3-anilino-5-methyl-5-(4-phenoxyphenyl)-13-oxazolidine-24-dione;
fenamidone, (S)-1-anilino-4-methyl-2-methylthio-4-phenylimidazolin-5-one;
octhilinone,
probenazole, 3-allyloxy-1,2-benzothiazole 1,1-dioxide;
amisulbrom, N,N-dimethyl-3-(3-bromo-6-fluoro-2-methylindole-1-sulfonyl)-
[1,2,4]triazole-1-sulfonamide (WO 03/053145);
anilazine, 4,6-dichloro-N-(2-chlorophenyl)-1,3,5-triazine-2-amine (US 2 720 480);
diclomezine, 6-(3,5-dichlorophenyl)-p-tolyl)pyridazin-3(2H)-one;
pyroquilon,
proquinazid, 6-iodo-2-propoxy-3-propylquinazolin-4(3H)-one (WO 97/48684);

PF 56951
8
tricyclazole, 5-methyl-1,2,4-triazolo[3,4-^benzothiazole (GB 14 19 121);
acibenzolar-S-methyl, methyl benzo[1,2,3]thiadiazole-7-carbothionate;
captafol, N-(1,1,2,2-tetrachloroethylthio)cyclohex-4-ene-1,2-dicarboximide;
captan, 2-trichloromethylsulfanyl-3a,4,7,7a-tetrahydroisoindole-1,3-dione (US
2 553 770);
dazomet, 3,5-dimethyl-1,3,5-thiadiazinane-2-thione;
folpet, 2-trichloromethylsulfanylisoindole-1,3-dione (US 2 553 770);
fenoxanil, N-(1-cyano-1,2-dimethylpropyl)-2-(2,4-dichlorophenoxy) propanamide;
quinoxyfen, 5,7-dichloro-4-(4-fluorophenoxy)quinoline (US 5 240 940);
mancozeb, manganese ethylenebis(dithiocarbanate) zinc complex (US 3 379 610);
maneb, manganese ethylenebis(dithiocarbamate) (US 2 504 404);
metam, methyldithiocarbaminic acid (US 2 791 605);
metiram, zinc ammoniate ethylenebis(dithiocarbamate) (US 3 248 400);
propineb, zinc propylenebis(dithiocarbamate) polymer (BE 611 960);
ferbam, iron(3+) dimethyldithiocarbamate (US 1 972 961);
thiram, bis(dimethylthiocarbamoyl) disulfide (DE 642 532);
ziram, dimethyldithiocarbamate;
zineb, zinc ethylenebis(dithiocarbamate) (US 2 457 674);
diethofencarb, isopropyl 3,4-diethoxycarbanilate;
iprovalicarb, isopropyl [(1S)-2-methyl-1 -(1-p-tolylethylcarbamoyl)propyl]carbamate
(EP-A 472 996);
flubenthiavalicarb (benthiavalicarb), isopropyl {(S)-1-[(1R)-1-(6-fluorobenzothiazol-2-yl)-
ethylcarbamoyl]-2-methylpropyl}carbamate (JP-A 09/323 984);
propamocarb, propyl 3-(dimethylamino)propylcarbamate (DE 16 43 040);
dodine, (2,4-dichlorophenoxy)acetic acid (US 2 867 562);
iminoctadine, bis(8-guanidinooctyl)amine (GB 11 14 155);
guazatine, mixture of products from the amidation of irninodi(octamethylene)diamine,
mainly iminoctadine;
kasugamycin, 1L-1,3,4/2,5,6-1-deoxy-2,3,4,5,6-pentahydroxycyclohexyl 2-amino-
2,3,4,6-tetradeoxy-4-(α-iminoglycino)-α-D-arabino-hexopyranoside;
streptomycin, O-2-deoxy-2-methylamino-a-L-glucopyranosyl-(1→2)-O-5-deoxy-3-C-
formyl-a-L-lyxofuranosyl-(1→4)N1,N3-diamidino-D-streptamine;
polyoxins, 5-(2-amino-5-O-carbamoy!-2-deoxy-L-xylonamido)-1-(5-carboxy-1,2,3,4-
tetrahydro-2,4-dioxopyrimidin-1-yl)-1,5-dideoxy-β-D-allofuranuronic acid and the salts
thereof;
validamycin A,
binapacryl, (RS)-2-sec-butyl-4,6-dinitrophenyl 3-methylcrotonate;
dinocap, the mixture of 2,6-dinitro-4-octylphenyl crotonate and 2,4-dinitro-6-octylphenyl
crotonate, wherein "octyl" is a mixture of 1-methylheptyl, 1-ethylhexyl and
1-propylpentyl (US 2 526 660);
dinobuton, (RS)-2-sec-butyl-4,6-dinitrophenyl isopropyl carbonate;
dithianon, 5,10-dioxo-5,10-dihydronaphtho[2,3-b][1,4]dithiin-2,3-dicarbonitrile

PF 56951
9
(GB 857 383);
isoprothiolane, indol-3-ylacetic acid;
fentin acetate, triphenyltin acetate (US 3 499 086);
edifenphos, O-ethyl S,S-diphenyl phosphorodithioate;
iprobenfos, S-benzyl O,O-diisopropyl phosphorothioate (Jpn. Pesticide Inf., No. 2, S.
11 (1970));
fosetyl, fosetyl-aluminum, (aluminum) ethylphosphonate (FR 22 54 276);
pyrazophos, ethyl 2-diethoxyphosphinothioyloxy-5-methylpyrazolo[1,5-a]pyrimidine-6-
carboxylate (DE 15 45 790);
tolclofos-methyl, O-2,6-dichloro-p-tolyl O,O-dimethyl phosphorothioate (GB 14 67 561);
chlorothalonil, 2,4,5,6-tetrachloroisophthalonitrile (US 3 290 353);
dichlofluanid, N-dichlorofluoromethylthio-N,N-dimethyl-N-phenylsulfamide (DE
11 93 498);
flusulfamide, 2',4-dichloro-α,α,α-trifluoro-4'-nitro-m-toluenesulfanilide (EP-A 199 433);
hexachlorobenzene (C. R. Seances Acad. Agric. Fr, Vol. 31, p. 24 (1945));
phthalide(DE16 43 347);
pencycuron, 1-(4-chlorobenzyl)-1-cyclopentyl-3-phenylurea (DE 27 32 257);
quintozene, pentachloronitrobenzene (DE 682 048);
thiophanate-methyl, 1,2-phenylenebis(iminocarbonothioyl)bis(dimethylcarbamate)
(DE-OS 19 30 540);
tolylfluanid, N-dichlorofluoromethylthio-N,N-dimethyl-N-p-tolylsulfamide
(DE 11 93 498);
Bordeaux mixture, mixture of calcium hydroxide and copper(ll) sulfate;
copper hydroxide, Cu(OH)2; copper oxychloride, Cu2CI(OH)3;
cyflufenamid, (Z)-N-[α-(cyclopropylmethoxyimino)-2,3-difluoro-6-(trifluoromethyl)ben-
zyl]-2-phenylacetamide (WO 96/19442);
cymoxanil, 1-(2-cyano-2-methoxyiminoacetyl)-3-ethylurea (US 3 957 847);
dimethirimol, 5-butyl-2-dimethylamino-6-methylpyrimidin-4-ol (GB 11 82 584);
ethirimol, 5-butyl-2-ethylamino-6-methylpyrimidin-4-ol (GB 11 82 584);
furalaxyl, methyl N-(2-furoyl)-N-(2,6-xylyl)-DL-alaninate (GB 14 48 810);
metrafenone, 3'-bromo-2,3,4,6'-tetramethoxy-2',6-dimethylbenzophenone (US
5 945 567);
spiroxamine, (8-tert-butyl-1,4-dioxaspiro[4.5]dec-2-yl)diethylamine (EP-A 281 842).
The compounds named according to IUPAC, their preparation and their fungicidal
action are likewise known:
methyl (2-chloro-5-[1-(3-methylbenzyloxyimino)ethyl]benzyl)carbamate, methyl (2-
chloro-5-[1-(6-methylpyridin-2-ylmethoxyimino)ethyl]benzyl)carbamate (EP-A
12 01 648);
methyl 2-(ortho-((2,5-dimethylphenyloxymethylene)phenyl)-3-methoxyacrylate (EP-A
226 917);
5-chloro-7-(4-methylpiperidin-1 -yl)-6-(2,4,6-trifluorophenyl)-[1,2,4]triazolo[1,5-a]pyri-
midine (WO 98/46608),

PF 56951
10
3,4-dichloro-N-(2-cyanophenyl)isothiazole-5-carboxamide (WO 99/24413),
N-(2-{4-[3-(4-chlorophenyl)prop-2-ynyloxy]-3-methoxyphenyl}ethyl)-2-methanesulfonyl-
amino-3-methylbutyramide, N-(2-{4-[3-(4-chlorophenyl)prop-2-ynyloxy]-3-methoxyphe-
nyl}ethyl)-2-ethanesulfonylamino-3-methylbutyramide (WO 04/049804),
N-(4'-bromobiphenyl-2-yl)-4-difluoromethyl-2-methylthiazole-5-carboxamide, N-(4'-
trifluoromethylbiphenyl-2-yl)-4-difluoromethyl-2-methylthiazole-5-carboxamide, N-(4'-
chloro-3'-fluorobiphenyl-2-yl)-4-difluoromethyl-2-methylthiazole-5-carboxamide, N-
(3',4'-dichloro-4-fluorobiphenyl-2-yl)-3-difluoromethyl-1-methylpyrazole-4-carboxamide
(WO 03/066609), N-(3',4'-dichloro-5-fluorobiphenyl-2-yl)-3-difluoromethyl-1-
methylpyrazole-4-carboxamide (WO 03/053145);
2-butoxy-6-iodo-3-propylchromen-4-one (WO 03/14103),
3-[5-(4-chlorophenyl)-2,3-dimethylisoxazolidin-3-yl]pyridine (EP-A 10 35 122);
amisulbrom, N,N-dimethyl-3-(3-bromo-6-fluoro-2-methylindole-1-sulfonyl)-
[1,2,4]triazole-1-sulfonamide (WO 03/053145),
methyl 3-(4-chlorophenyl)-3-(2-isopropoxycarbonylamino-3-methylbutyrylamino)-
propanoate (EP-A 1028125).
It is an object of the present invention, with a view to reducing the application rates and
broadening the activity spectrum of the known compounds, to provide mixtures which,
at a reduced total amount of active compounds applied, have improved activity against
harmful fungi, in particular for certain indications.
We have found that this object is achieved by the mixtures defined at the outset.
Moreover, we have found that simultaneous, that is joint or separate, application of the
compounds I and an active compound II or successive application of the compounds I
and an active compound II allows better control of harmful fungi than is possible with
the individual compounds (synergistic mixtures). The compounds I can be used as a
synergist for a large number of different active compounds. The simultaneous, that is
joint or separate, application of the compound I with an active compound II increases
the fungicidal activity in a superadditive manner.
The mixtures of the compounds I and an active compound II or the simultaneous, that
is joint or separate, use of the compounds I and an active compound II are/is
distinguished by excellent activity against a broad spectrum of phytopathogenic fungi,
in particular from the classes of the Ascomycetes, Deuteromycetes, Oomycetes and
Basidiomycetes. Some of them are systemically active and can be used in crop
protection as foliar fungicides, as fungicides for seed dressing and as soil fungicides.
They are particularly important in the control of a multitude of fungi on various crop
plants, such as bananas, cotton, vegetables (for example cucumbers, beans and
cucurbits), barley, grass, oats, coffee, potatoes, corn, fruit, rice, rye, soybeans,
tomatoes, grape vines, wheat, ornamental plants, sugar cane and a multiplicity of

PF 56951
11
seeds.
Advantageously, they are suitable for controlling the following plant diseases:
• Alternaria species on vegetables, oilseed rape, sugar beet and fruit and rice, such
as, for example, A. solam'or A. alternata on potatoes and tomatoes;
• Aphanomyces species on sugar beet and vegetables;
• Ascochyta species on cereals and vegetables;
• Bipolaris and Drechslera species on corn, cereals, rice and lawns, such as, for
example, D. maydis on corn;
• Blumeria graminis (powdery mildew) on cereals;
• Botrytis cinerea (gray mold) on strawberries, vegetables, flowers and grapevines;
• Bremia lactucae on lettuce;
• Cercospora species on corn, soybeans, rice and sugar beet;

• Cochliobolus species on corn, cereals, rice, such as, for example, Cochliobolus
sativus on cereals, Cochliobolus miyabeanus on rice;
• Colletotricum species on soybeans and cotton;
• Drechslera species, Pyrenophora species on corn, cereals, rice and lawns, such
as, for example, D. teres on barley or D. tritici-repentis on wheat;
• Esca on grapevines, caused by Phaeoacremonium chlamydosporium,
Ph. Aleophilum and Formitipora punctata (syn. Phellinus punctatus),
• Exserohilum species on corn;
• Erysiphe cichoracearum and Sphaerotheca fuliginea on cucumbers;
• Fusarium and Verticillium species on various plants, such as, for example,
F. graminearum or F. culmorum on cereals or F. oxysporum on a multitude of
plants, such as, for example, tomatoes;
• Gaeumanomyces graminis on cereals;
• Gibberella species on cereals and rice (for example Gibberella fujikuroi on rice);
• Grainstaining complex on rice;
• Helminthospohum species on corn and rice;
• Michrodochium nivale on cereals;
• Mycosphaerella species on cereals, bananas and groundnuts, such as, for
example, M. graminicola on wheat or M.fijiensis on bananas;
• Peronospora species on cabbage and bulbous plants, such as, for example,
P. brassicae on cabbage or P. destructor on onions;
• Phakopsara pachyrhizi and Phakopsara meibomiae on soybeans;
• Phomopsis species on soybeans and sunflowers;
• Phytophthora infestans on potatoes and tomatoes;
• Phytophthora species on various plants, such as, for example, P. capsici on bell
pepper;
• Plasmopara viticola on grapevines;
• Podosphaera leucotricha on apples;

PF 56951
12
• Pseudocercosporella herpotrichoides on cereals;
• Pseudoperonospora on various plants, such as, for example, P. cubensis on
cucumber or P. humillion hops;
• Puccinia species on various plants, such as, for example, P. triticina, P. striformins,
P. horde/or P.graminis on cereals or P. asparagi on asparagus;
• Pyricularia oryzae, Corticium sasakii, Sarocladium oryzae, S.attenuatum,
Entyloma oryzae on rice;
• Pyricularia grisea on lawns and cereals;
• Pythium spp. on lawns, rice, com, cotton, oilseed rape, sunflowers, sugar beet,
vegetables and other plants, such as, for example, P. ultiumum on various plants,
P. aphanidermatum on lawns;
• Rhizoctonia species on cotton, rice, potatoes, lawns, corn, oilseed rape, potatoes,
sugar beet, vegetables and on various plants, such as, for example, R. solani on
beet and various plants;
• Rhynchosporium secalis on barley, rye and triticale;
• Sclerotinia species on oilseed rape and sunflowers;
• Septoria tritici and Stagonospora nodorum on wheat;
• Erysiphe (syn. Uncinula) necator on grapevines;
• Setospaeria species on corn and lawns;
• Sphacelotheca reilinia on corn;
• Thievaliopsis species on soybeans and cotton;
• Tilletia species on cereals;
• Ustilago species on cereals, com and sugar cane, such as, for example, U. maydis
on corn;
• Venturia species (scab) on apples and pears, such as, for example, V. inaequalis
on apples.
The mixtures of the compounds I and active compounds II are suitable in particular for
controlling harmful fungi from the class of the Peronosporomycetes (syn. Oomycetes),
such as Peronospora species, Phytophthora species, Plasmopara viticola and
Pseudoperonospora species, in particular fungi corresponding to those mentioned
above.
The compounds I and active compounds II can be applied simultaneously, that is jointly
or separately, or in succession, the sequence, in the case of separate application,
generally not having any effect on the result of the control measures.
In the definitions of the symbols given for the formulae above, collective terms were
used which generally represent the following substituents:
halogen: fluorine, chlorine, bromine and iodine;

PF 56951
13
alkyl: saturated straight-chain or branched hydrocarbon radicals having 1 to 4, 6, 8 or
10 carbon atoms, for example C1-C6-alkyl, such as methyl, ethyl, propyl, 1-methylethyl,
butyl, 1-methylpropyl, 2-methylpropyl, 1,1-dimethylethyl, pentyl, 1-methylbutyl, 2-me-
thylbutyl, 3-methylbutyl, 2,2-dimethylpropyl, 1-ethylpropyl, hexyl, 1,1-dimethylpropyl,
1,2-dimethylpropyl, 1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl,
1,1-dimethylbutyl, 1,2-dimethylbutyl, 1,3-dimethylbutyl, 2,2-dimethylbutyl, 2,3-dime-
thylbutyl, 3,3-dimethylbutyl, 1-ethylbutyl, 2-ethylbutyl, 1,1,2-trimethylpropyl, 1,2,2-tri-
methylpropyl, 1-ethyl-1-methylpropyl and 1-ethyl-2-methylpropyl;
haloalkyl: straight-chain or branched alkyl groups having 1 to 2, 4 or 6 carbon atoms
(as mentioned above), where some or all of the hydrogen atoms in these groups may
be replaced by halogen atoms as mentioned above: in particular C1-C2-haloalkyl, such
as chloromethyl, bromomethyl, dichloromethyl, trichloromethyl, fluoromethyl,
difluoromethyl, trifluoromethyl, chlorofluoromethyl, dichlorofluoromethyl,
chlorodifluoromethyl, 1-chloroethyl, 1-bromoethyl, 1-fluoroethyl, 2-fluoroethyl, 2,2-
difluoroethyl, 2,2,2-trifluoroethyl, 2-chloro-2-fluoroethyl, 2-chloro-2,2-difluoroethyl, 2,2-
dichloro-2-fluoroethyl, 2,2,2-trichloroethyl, pentafluoroethyl or 1,1,1 -trifluoroprop-2-yl.
With a view to the intended use of the azolopyhmidinylamines of the formula I,
particular preference is given to the following meanings of the substituents, in each
case on their own or in combination:
Particularly suitable for the mixtures according to the invention are compounds of the
formula I in which R1 is straight-chain or branched C3-C12-alkyl or phenyl which may be
substituted by one to three halogen or C1-C4-alkyl groups.
In one embodiment of the compounds of the formula I, group Ra is absent.
A preferred embodiment relates to compounds of the formula I in which R1 is straight-
chain or branched C5-C10-alkyl, in particular ethyl, 3,5,5-trimethylhexyl, n-heptyl, n-
octyl, n-nonyl and n-decyl.
A further embodiment relates to the compounds of the formula I in which R1 is phenyl
which is unsubstituted or substituted by one to four halogen, cyano, hydroxyl,
mercapto, nitro, NRARB, C1-C10-alkyl, C1-C6-haloalkyl, C2-C6-alkenyl, C2-C6-alkynyl and
C1-C6-alkoxy groups.
Preferred compounds of the formula I are those in which R1 is a substituted phenyl
group which corresponds to a group G

PF 56951
14

in which
L1 is cyano, halogen, hydroxyl, mercapto, nitro, NRARB, C1-C10-alkyl, C1-C6-
haloalkyl, C2-C6-alkenyl, C2-C6-alkynyl and C1-C6-alkoxy; and
L2,L3 independently of one another are hydrogen or one of the groups mentioned
under L1 and
# denotes the bond to the azolopyrimidine skeleton.
In a further embodiment of the compounds of the formula I, L1 is cyano, halogen,
hydroxyl, mercapto, nitro, NRARB, C1-C6-alkyl, halomethyl or C1-C2-alkoxy, preferably
cyano, halogen, C1-C6-alkyl, halomethyl or C1-C2-alkoxy.
In a further embodiment of the compounds of the formula I, L2 is hydrogen or one of the
groups mentioned above.
In a further embodiment of the compounds of the formula I, L3 is hydrogen, cyano,
halogen, hydroxyl, mercapto, nitro, NRARB, C1-C6-alkyl, halomethyl or C1-C2-alkoxy,
preferably hydrogen.
Preference is given to compounds of the formula I in which R2 is straight-chain or
branched C1-C12-alkyl, C1-C4-alkoxy-C1-C4-alkyl or C1-C4-haloalkyl.
In a particularly preferred embodiment of the compounds of the formula I, R2 is methyl,
ethyl, n-propyl, n-octyl, trifluoromethyl or methoxymethyl, in particular methyl, ethyl,
trifluoromethyl or methoxymethyl.
Preference is furthermore given to compounds of the formula I in which R3 is hydrogen.
In a further embodiment of the compounds of the formula I, R3 is amino.
One embodiment of the compounds of the formula I relates to those in which A'is N.
These compounds correspond to the formula IA in which the variables are as defined
for formula I:
Another embodiment of the compounds of the formula I relates to those in which A is
CH. These compounds correspond to the formula IB in which the variables are as

PF 56951
15
defined for formula I:
In a further embodiment of preferred compounds I, the carbon chains of R1 and R2
together do not have more than 12 carbon atoms.
Especially preferred with a view to their use are the compounds I compiled in the tables
below. The groups mentioned for a substituent in the tables are furthermore per se,
independently of the combination in which they are mentioned, a particularly preferred
embodiment of the substituent in question.
Table 1
Compounds of the formula IA in which the combination of R1, R2 and R3 for a
compound corresponds in each case to one row of Table I
Table 2
Compounds of the formula IB in which the combination of R1, R2 and R3 for a
compound corresponds in each case to one row of Table I
Table I

PF 56951
16

PF 56951
17

PF 56951
18

PF 56951
19

PF 56951
20

PF 56951
21

PF 56951
22

PF 56951
23
Preferred embodiments of the mixtures according to the invention comprise, as active
component 1, a compound selected from the following list:
6-(3,4-dichlorophenyl)-5-methyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine,
6-(4-tert-butylphenyl)-5-methyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine,
5-methyl-6-(3,5,5-trimethylhexyl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine,
5-methyl-6-octyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine,
5-ethyl-6-octyl-[1,2,4]triazolo[1,5-a]pyrimidine-2,7-diamine,
6-ethyl-5-octyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine,
5-ethyl-6-octyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine,
5-ethyl-6-(3,5,5-trimethylhexyl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine,
6-octyl-5-propyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine,
5-methoxymethyl-6-octyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine,
6-octyl-5-trifluoromethyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine and
5-trifluoromethyl-6-(3,5,5-trimethylhexyl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine.
Further preferred embodiments of the mixtures according to the invention relate to
combinations of one of the compounds of Table 1, in particular one of the preferred
compounds I hereinabove, and one of the following active compounds II:
A) azoles, such as cyproconazole, difenoconazole, fluquinconazole,
flusilazole, metconazole, propiconazole, prothioconazole, tebuconazole
prochloraz, cyazofamid;
carbendazim;
ethaboxam;
B) strobilurins, such as azoxystrobin, enestroburin, fluoxastrobin, pyraclo-
strobin, trifloxystrobin or methyl (2-chloro-5-[1-(3-methylbenzyloxyimino)-
ethyl]benzyl)carbamate [B-6], methyl (2-chloro-5-[1-(6-methylpyridin-2-yl-
methoxyimino)ethyl]benzyl)carbamate [B-7];
C) carboxamides, such as benalaxyl, boscalid, metalaxyl, ofurace, oxadixyl,
dimethomorph;
fluopicolide (picobenzamid), zoxamide;
mandipropamid;
D) heterocylic compounds, such as fluazinam;
cyprodinil, pyrimethanil;
dodemorph,
iprodione, vinclozolin;
famoxadone, fenamidone;
amisulbrom;

PF 56951
24
5-chloro-7-(4-methylpiperidin-1-yl)-6-(2,4,6-trifluorophenyl)-[1,2,4]tri-
azolo[1,5-a]pyrimidine [D-8],
captan, folpet;
E) carbamates, such as mancozeb, maneb, metiram, propineb;
iprovalicarb, flubenthiavalicarb;
methyl 3-(4-chlorophenyl)-3-(2-isopropoxycarbonylamino-3-methyl-
butyrylamino)propanoate [E-7];
and
F) other active compounds, selected from
sulfur-containing heterocyclyl compounds: dithianon;
organophosphorus compounds: fosetyl, fosetyl-aluminum, phosphorous
acid and its salts;
organochlorine compounds: chlorothalonil, thiophanate-methyl;
inorganic active compounds: Bordeaux mixture, copper acetate, copper
hydroxide, copper oxychloride, basic copper sulfate;
others: cymoxanil, metrafenone;
growth retardants: prohexadione and its salts.
Preferred embodiments relate to the compositions listed in table A, where in each case
one row of table A corresponds to a fungicidal composition comprising the particular
compound of the formula I mentioned (component 1) and one active compound of the
groups mentioned, this active compound preferably being selected from the preferred
embodiments defined above.
Table A

PF 56951
25

PF 56951
26

The active compounds mentioned above can also be employed in the form of their
agriculturally compatible salts. These are usually the alkali metal or alkaline earth metal
salts, such as sodium, potassium or calcium salts.
When preparing the mixtures, preference is given to using the pure active compounds
which, if required, may be mixed with further active compounds against harmful fungi or
other pests, such as insects, arachnids or nematodes, or else herbicidal or growth-
regulating active compounds or fertilizers as further active components.
In a preferred embodiment of the invention, mixtures of an azolopyrimidinylamine and
an active compound II are used. Under certain conditions, it may be advantageous to
combine an azolopyrimidinylamine with two or more active compounds II. In addition,
mixtures of two or more compounds I with one or more active compounds II may also
be suitable.
Suitable further active components in the above sense are in particular the active
compounds II, mentioned at the outset, and in particular the preferred active
compounds mentioned above. In the case of ternary mixtures, preferred third active
components are strobilurins, in particular pyraclostrobin, carboxamides, in particular
boscalid, and also organophosphorus compounds, in particular phosphorous acid and
its salts.
The compounds I and active compounds II are usually employed in a weight ratio of

PF 56951
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from 100:1 to 1:100, preferably from 50:1 to 1:50, preferably from 20:1 to 1:20, in
particular from 10:1 to 1:10.
The further active components are, if desired, added in a ratio of from 50:1 to 1:50,
preferably from 20:1 to 1:20, to the compound I.
Depending on the type of compound and the desired effect, the application rates of the
mixtures according to the invention are from 5 g/ha to 2000 g/ha, preferably from 50 to
900 g/ha, in particular from 50 to 750 g/ha.
Correspondingly, the application rates for compounds I are generally from 1 to 1000
g/ha, preferably from 10 to 900 g/ha, in particular from 20 to 750 g/ha.
Depending on the type of active compound II, the application rates for active
compounds II are generally from 1 to 2000 g/ha, preferably from 10 to 900 g/ha, in
particular from 40 to 500 g/ha.
In the treatment of seed, for example by dusting, coating or soaking seeds, application
rates of mixture are generally from 1 to 1000 g/100 kg of seed, preferably from 1 to 750
g/100 kg, in particular from 5 to 500 g/100 kg.
The method for controlling harmful fungi is carried out by the separate or joint
application of the compounds I and active compounds II or the mixtures of compounds
I and active compounds II by spraying or dusting the seeds, the plants or the soils
before or after sowing of the plants or before or after emergence of the plants.
The mixtures according to the invention, or the compounds I and active compounds II
can be converted into the customary formulations, for example solutions, emulsions,
suspensions, dusts, powders, pastes and granules. The use form depends on the
particular intended purpose; in each case, it should ensure a fine and even distribution
of the compound according to the invention.
The formulations are prepared in a known manner, for example by extending the active
compound with solvents and/or carriers, if desired using emulsifiers and dispersants.
Solvents/auxiliaries suitable for this purpose are essentially:
water, aromatic solvents (for example Solvesso products, xylene), paraffins (for
example mineral oil fractions), alcohols (for example methanol, butanol, pentanol,
benzyl alcohol), ketones (for example cyclohexanone, gamma-butyrolactone),
pyrrolidones (NMP, NOP), acetates (glycol diacetate), glycols, fatty acid
dimethylamides, fatty acids and fatty acid esters. In principle, solvent mixtures may
also be used,
carriers such as ground natural minerals (for example kaolins, clays, talc, chalk)

PF 56951
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and ground synthetic minerals (for example highly disperse silica, silicates);
emulsifiers such as nonionogenic and anionic emulsifiers (for example
polyoxyethylene fatty alcohol ethers, alkylsulfonates and arylsulfonates) and
dispersants such as lignosulfite waste liquors and methylcellulose.
Suitable surfactants used are alkali metal, alkaline earth metal and ammonium salts of
lignosulfonic acid, naphthalenesulfonic acid, phenolsulfonic acid,
dibutylnaphthalenesulfonic acid, alkylarylsulfonates, alkyl sulfates, alkylsulfonates, fatty
alcohol sulfates, fatty acids and sulfated fatty alcohol glycol ethers, furthermore
condensates of sulfonated naphthalene and naphthalene derivatives with
formaldehyde, condensates of naphthalene or of naphthalenesulfonic acid with phenol
and formaldehyde, polyoxyethylene octylphenyl ether, ethoxylated isooctylphenol,
octylphenol, nonylphenol, alkylphenyl polyglycol ethers, tributylphenyl polyglycol ether,
tristearylphenyl polyglycol ether, alkylaryl polyether alcohols, alcohol and fatty alcohol
ethylene oxide condensates, ethoxylated castor oil, polyoxyethylene alkyl ethers,
ethoxylated polyoxypropylene, lauryl alcohol polyglycol ether acetal, sorbitol esters,
lignosulfite waste liquors and methylcellulose.
Substances which are suitable for the preparation of directly sprayable solutions,
emulsions, pastes or oil dispersions are mineral oil fractions of medium to high boiling
point, such as kerosene or diesel oil, furthermore coal tar oils and oils of vegetable or
animal origin, aliphatic, cyclic and aromatic hydrocarbons, for example toluene, xylene,
paraffin, tetrahydronaphthalene, alkylated naphthalenes or their derivatives, methanol,
ethanol, propanol, butanol, cyclohexanol, cyclohexanone, isophorone, highly polar
solvents, for example dimethyl sulfoxide, N-methylpyrrolidone and water.
Powders, materials for spreading and dustable products can be prepared by mixing or
concomitantly grinding the active substances with a solid carrier.
Granules, for example coated granules, impregnated granules and homogeneous
granules, can be prepared by binding the active compounds to solid carriers. Examples
of solid carriers are mineral earths such as silica gels, silicates, talc, kaolin, attaclay,
limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium sulfate.
magnesium sulfate, magnesium oxide, ground synthetic materials, fertilizers, such as,
for example, ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas, and
products of vegetable origin, such as cereal meal, tree bark meal, wood meal and
nutshell meal, cellulose powders and other solid carriers.
Formulations for the treatment of seed may additionally comprise binders and/or gelling
agents and, if appropriate, colorants.
In general, the formulations comprise from 0.01 to 95% by weight, preferably from 0.1

PF 56951
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to 90% by weight, of the active compounds. The active compounds are employed in a
purity of from 90% to 100%, preferably 95% to 100%.
For the treatment of seed, the formulations in question give, after two-to-tenfold
dilution, active compound concentrations of from 0.01 to 60% by weight, preferably
from 0.1 to 40% by weight, in the ready-to-use preparations.
The following are examples of formulations according to the invention:
1. Products for dilution with water
A Water-soluble concentrates (SL, LS)
10 parts by weight of a mixture according to the invention are dissolved in 90 parts by
weight of water or in a water-soluble solvent. As an alternative, wetters or other
auxiliaries are added. The active compound dissolves upon dilution with water. In this
way, a formulation having a content of 10% by weight of active compound is obtained.
B Dispersible concentrates (DC)
20 parts by weight of a mixture according to the invention are dissolved in 70 parts by
weight of cyclohexanone with addition of 10 parts by weight of a dispersant, for
example polyvinylpyrrolidone. Dilution with water gives a dispersion. The active
compound content is 20% by weight.
C Emulsifiable concentrates (EC)
15 parts by weight of a mixture according to the invention are dissolved in 75 parts by
weight of xylene with addition of calcium dodecylbenzenesulfonate and castor oil
ethoxylate (in each case 5 parts by weight). Dilution with water gives an emulsion. The
formulation has an active compound content of 15% by weight.
D Emulsions (EW, EO, ES)
25 parts by weight of a mixture according to the invention are dissolved in 35 parts by
weight of xylene with addition of calcium dodecylbenzenesulfonate and castor oil
ethoxylate (in each case 5 parts by weight). This mixture is introduced into 30 parts by
weight of water by means of an emulsifying machine (Ultraturrax) and made into a
homogeneous emulsion. Dilution with water gives an emulsion. The formulation has an
active compound content of 25% by weight.
E Suspensions (SC, OD, FS)
In an agitated ball mill, 20 parts by weight of a mixture according to the invention are
comminuted with addition of 10 parts by weight of dispersants and wetters and 70 parts
by weight of water or an organic solvent to give a fine active compound suspension.
Dilution with water gives a stable suspension of the active compound. The active
compound content in the formulation is 20% by weight.

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F Water-dispersible granules and water-soluble granules (WG, SG)
50 parts by weight of a mixture according to the invention are ground finely with
addition of 50 parts by weight of dispersants and wetters and prepared as water-
dispersible or water-soluble granules by means of technical appliances (for example
extrusion, spray tower, fluidized bed). Dilution with water gives a stable dispersion or
solution of the active compound. The formulation has an active compound content of
50% by weight.
G Water-dispersible powders and water-soluble powders (WP, SP, SS, WS)
75 parts by weight of a mixture according to the invention are ground in a rotor-stator
mill with addition of 25 parts by weight of dispersants, wetters and silica gel. Dilution
with water gives a stable dispersion or solution of the active compound. The active
compound content of the formulation is 75% by weight.
H Gel formulations
In a ball mill, 20 parts by weight of a mixture according to the invention, 10 parts by
weight of dispersant, 1 part by weight of gelling agent and 70 parts by weight of water
or an organic solvent are ground to give a fine suspension. On dilution with water, a
stable suspension having an active compound content of 20% by weight is obtained.
2. Products to be applied undiluted
I Dustable powders (DP, DS)
5 parts by weight of a mixture according to the invention are ground finely and mixed
intimately with 95 parts by weight of finely divided kaolin. This gives a dustable product
having an active compound content of 5% by weight.
J Granules (GR, FG, GG, MG)
0.5 part by weight of a mixture according to the invention is ground finely and
associated with 99.5 parts by weight of carriers. Current methods are extrusion, spray-
drying or the fluidized bed. This gives granules to be applied undiluted having an active
compound content of 0.5% by weight.
K ULV solutions (UL)
10 parts by weight of a mixture according to the invention are dissolved in 90 parts by
weight of an organic solvent, for example xylene. This gives a product to be applied
undiluted having an active compound content of 10% by weight.
For seed treatment, use is usually made of water-soluble concentrates (LS),
suspensions (FS), dustable powders (DS), water-dispersible and water-soluble
powders (WS, SS), emulsions (ES), emulsifiable concentrates (EC) and gel

PF 56951
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formulations (GF). These formulations can be applied to the seed in undiluted form or,
preferably, diluted. Application can be carried out prior to sowing.
Preference is given to using FS formulations for seed treatment. Usually, such
formulations comprise from 1 to 800 g of active compound/I, from 1 to 200 g of
surfactants/I, from 0 to 200 g of antifreeze agents/I, from 0 to 400 g of binder/I, from 0
to 200 g of colorants/I and solvents, preferably water.
Analogous formulations A to K of the compounds I or an active compound II comprise
the respective amount of the individual active compounds. They are usually mixed
directly prior to application during dilution to the ready-to-use active compound
concentration (tank mix).
The active compound concentrations in the ready-to-use preparations may be varied
within relatively wide ranges. In general, they are between 0.0001 and 10%, preferably
between 0.01 and 1%.
The active compounds can be used as such, in the form of their formulations or the use
forms prepared therefrom, for example in the form of directly sprayable solutions,
powders, suspensions or dispersions, emulsions, oil dispersions, pastes, dustable
products, materials for spreading, or granules, by means of spraying, atomizing,
dusting, spreading or pouring. The use forms depend entirely on the intended
purposes; they are intended to ensure in each case the finest possible distribution of
the active compounds according to the invention.
Aqueous use forms can be prepared from emulsion concentrates, pastes or wettable
powders (wettable powders, oil dispersions) by adding water. To prepare emulsions,
pastes or oil dispersions, the substances, as such or dissolved in an oil or solvent, can
be homogenized in water by means of a wetter, tackifier, dispersant or emulsifier.
However, it is also possible to prepare concentrates composed of active substance,
wetter, tackifier, dispersant or emulsifier and, if appropriate, solvent or oil, and such
concentrates are suitable for dilution with water.
The active compounds may also be used successfully in the ultra-low-volume process
(ULV), it being possible to apply formulations comprising over 95% by weight of active
compound, or even to apply the active compound without additives.
Oils of various types, wetters, adjuvants, herbicides, fungicides, other pesticides, or
bactericides may be added to the active compounds, even, if appropriate, not until
immediately prior to use (tank mix). These agents may be admixed with the
compositions according to the invention in a weight ratio of from 1:100 to 100:1,
preferably from 1:10 to 10:1.

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Suitable adjuvants in this sense are in particular: organically modified polysiloxanes,
for example Break Thru S 240®; alcohol alkoxylates, for example Atplus 245®, Atplus
MBA 1303®, Plurafac LF 300® and Lutensol ON 30®; EO/PO block polymers, for
example Pluronic RPE 2035® and Genapol B®; alcohol ethoxylates, for example
Lutensol XP 80®; and sodium dioctylsulfosuccinate, for example Leophen RA®.
The compounds I and II or the mixtures or the corresponding formulations are applied
by treating the harmful fungi, the plants, seeds, soils, areas, materials or spaces to be
kept free from them with a fungicidally effective amount of the mixture or, in the case of
separate application, of the compounds I and II. Application can be carried out before
or after infection by the harmful fungi.
Use examples
The fungicidal effect of the compounds and the mixtures was demonstrated by the
following tests:
The active compounds amisulbrom, Cu hydroxide, famoxadone, phosphorous acid and
zoxamide were used as commercial formulations and diluted with water to the stated
concentrations.
The active compounds were separately or jointly prepared as a stock solution
comprising 25 mg of active compound which was made up to 10 ml using a mixture of
acetone and/or DMSO and the emulsifier Uniperol® EL (wetting agent having
emulsifying and dispersing action based on ethoxylated alkylphenols) in a volume ratio
of solvent/emulsifier of 99 to 1. The mixture was then made up with water to 100 ml.
This stock solution was diluted with the solvent/emulsifier/water mixture described to
the concentration of active compound stated below.
Use example 1 - Persistency against late blight on tomatoes caused by Phytophthora
infestans
Leaves of potted plants of the cultivar "Great beef tomato St. Pierre" were sprayed to
runoff point with an aqueous suspension having the concentration of active compound
stated below. After 5 days, the leaves were inoculated with an aqueous spore suspension
of Phytophthora infestans. The plants were then placed in a water vapor-saturated
chamber at temperatures between 18 and 20°C. After 6 days, the late blight on the
untreated but infected control plants had developed to such an extent that the infection
could be determined visually in %.
The visually determined percentages of infected leaf areas were converted into

PF 56951
33
efficacies in % of the untreated control:
The efficacy (E) is calculated as follows using Abbot's formula:
E = (1-α/β).100
α corresponds to the fungicidal infection of the treated plants in % and
β corresponds to the fungicidal infection of the untreated (control) plants in %
An efficacy of 0 means that the infection level of the treated plants corresponds to that
of the untreated control plants; an efficacy of 100 means that the treated plants were
not infected.
The expected efficacies of active compound combinations were determined using
Colby's formula (Colby, S.R. "Calculating synergistic and antagonistic responses of
herbicide combinations", Weeds, 15, 20-22, 1967) and compared with the observed
efficacies.
Colby's formula:
E = x + y-x. y/100
E expected efficacy, expressed in % of the untreated control, when using the
mixture of the active compounds A and B at the concentrations a and b
x efficacy, expressed in % of the untreated control, when using the active
compound A at the concentration a
y efficacy, expressed in % of the untreated control, when using the active
compound B at the concentration b
Table A - Individual active compounds

PF 56951
34

PF 56951
35

*) efficacy calculated using Colbys formula
Use example 2 - Activity against late blight on tomatoes caused by Phytophthora
infestans, protective treatment
Leaves of potted tomato plants were sprayed to runoff point with an aqueous suspension

PF 56951
36
having the active compound concentration stated below. After seven days, the leaves
were infected with an aqueous sporangia suspension of Phytophthora infestans. The
plants were then placed in a water vapor-saturated chamber at temperatures between 18
and 20°C. After 6 days, the late blight on the untreated but infected control plants had
developed to such an extent that the infection could be determined visually in %.
Evaluation was carried out analogously to example 1.

Use example 3 - Activity against peronospora of grapevines caused by Plasmopara
viticola
Leaves of potted grapevines were sprayed to runoff point with an aqueous suspension
having the active compound concentration stated below. After three days, the
undersides of the leaves were inoculated with an aqueous sporangia suspension of
Plasmopara viticola. The vines were then initially placed in a water vapor-saturated
chamber at 24°C for 24 hours and then in a greenhouse at temperatures between 20
and 30°C for 5 days. After this time, the plants were again placed in a humid chamber
for 16 hours to promote sporangiophore eruption. The extent of the development of the
infection on the undersides of the leaves was then determined visually.
Evaluation was carried out analogously to example 1.

PF 56951
37

Use example 4 - Activity against peronospora of grapevines caused by Plasmopara
viticola
Leaves of potted grapevines were sprayed to runoff point with an aqueous suspension
having the active compound concentration stated below. After seven days, the
undersides of the leaves were inoculated with an aqueous sporangia suspension of
Plasmopara viticola. The vines were then initially placed in a water vapor-saturated
chamber at 24°C for 24 hours and then in a greenhouse at temperatures between 20
and 30°C for 5 days. After this time, the plants were again placed in a humid chamber
for 16 hours to promote sporangiophore eruption. The extent of the development of the
infection on the undersides of the leaves was then determined visually.
Evaluation was carried out analogously to example 1.

PF 56951
38

Microtests
The active compounds were formulated separately as a stock solution of a concentration
of 10 000 ppm in DMSO.
The active compounds fluazinam, pyraclostrobin, copper hydroxide, flubenthiavalicarb,
phosphorous acid, dodemorph, zoxamide, amidosulbrom and trifloxystrobin were used
as commercial formulations and diluted with water to the stated concentrations.
Use example 5 - Activity against the late blight pathogen Phytophthora infestans in the
microtiter test
The stock solution is pipetted onto a microtiter plate (MTP) and diluted to the stated
active compound concentration using a pea juice-based aqueous nutrient medium for
fungi. An aqueous zoospore suspension of Phytophthora infestans was then added.
The plates were placed in a water vapor-saturated chamber at temperatures of 18°C.
Using an absorption photometer, the MTPs were measured at 405 nm on day 7 after
the inoculation.
The measured parameters were compared to the growth of the active compound-free
control variant and the fungus- and active compound-free blank value to determine the
relative growth in % of the pathogens in the individual active compounds.

PF 56951
39

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40

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41

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42

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43

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44

PF 56951
45
Use example 6 - Activity against the gray mold pathogen Botrytis cinerea in the microtiter
test
The stock solution is pipetted onto a microtiter plate (MTP) and diluted to the stated
active compound concentration using a malt-based aqueous nutrient medium for fungi.
An aqueous spore suspension of Botrytis cinerea was then added. The plates were
placed in a water vapor-saturated chamber at temperatures of 18°C. Using an
absorption photometer, the MTPs were measured at 405 nm on day 7 after the
inoculation.
Evaluation was carried out analogously to example 5.

PF 56951
46

PF 56951
47
Use example 7 - Activity against the rice blast pathogen Pyricularia oryzae in the
microtiter test
The stock solutions were mixed according to the ratio, pipetted onto a microtiter plate
(MTP) and diluted to the stated active compound concentration using a malt-based
aqueous nutrient medium for fungi. An aqueous spore suspension of Pyricularia oryzae
was then added. The plates were placed in a water vapor-saturated chamber at
temperatures of 18°C. Using an absorption photometer, the MTPs were measured at
405 nm on day 7 after the inoculation.
Evaluation was carried out analogously to example 5.

PF 56951
48

PF 56951
49

Use example 8 - Activity against the speckled leaf blotch pathogen Septoria tritici in the
microtiter test
The stock solution was mixed according to the ratio, pipetted onto a microtiter plate
(MTP) and diluted to the stated active compound concentration using a malt-based
aqueous nutrient medium for fungi. An aqueous spore suspension of Septoria tritici
was then added. The plates were placed in a water vapor-saturated chamber at
temperatures of 18°C. Using an absorption photometer, the MTPs were measured at
405 nm on day 7 after the inoculation.
Evaluation was carried out analogously to example 5.

The test results show that, by virtue of the synergism, the mixtures according to the
invention are considerably more effective than had been predicted using Colby's
formula.

PF 56951
50
Claims
1. A fungicidal mixture comprising, as active components:
1) azolopyrimidinylamines of the formula I,

in which the substituents are as defined below:
R1 is C3-C12-alkyl, C2-C12-alkenyl, C5-C12-alkoxyalkyl, C3-C6-cycloalkyl,
phenyl or phenyl-C1-C4-alkyl;
R2 is C1-C12-alkyl, C2-C12-alkenyl, C1-C4-haloalkyl, C1-C4-alkoxy-C1-C4-
alkyl;
where the aliphatic chains in R1 and/or R2 may be substituted by one
to four identical or different groups Ra:
Ra is halogen, cyano, hydroxyl, mercapto, C1-C10-alkyl, C1-C10-
haloalkyl, C3-C8-cycloalkyl, C2-C10-alkenyl, C2-C10-alkynyl, C1-
C6-alkoxy, C1-C6-alkylthio, C1-C6-alkoxy-C1-C6-alkyl or NRARB-
RA, RB are hydrogen and C1-C6-alkyl;
where the cyclic groups in R1 and/or Ra may be substituted by one to
four groups Rb:
Rb is halogen, cyano, hydroxyl, mercapto, nitro, NRARB, C1-C10-al-
kyl, C1-C6-haloalkyl, C2-C6-alkenyl, C2-C6-alkynyl or C1-C6-
alkoxy;
R3 is hydrogen, halogen, cyano, NRARB, hydroxyl, mercapto, C1-C6-alkyl,
C1-C6-haloalkyl, C3-C8-cycloalkyl, C1-C6-alkoxy, C1-C6-alkylthio, C3-
C8-cycloalkoxy, C3-C8-cycloalkylthio, carboxyl, formyl, C1-C10-
alkylcarbonyl, C1-C10-alkoxycarbonyl, C2-C10-alkeny!oxycarbonyl, C2-
C10-alkynyloxycarbonyl, phenyl, phenoxy, phenylthio, benzyloxy,
benzylthio, C1-C6-alkyl-S(O)m-;
m is 0, 1 or 2;
A is CR3 or N;
and
2) at least one active compound II selected from the following groups:

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51
A) azoles, such as bitertanol, bromuconazole, cyproconazole,
difenoconazole, diniconazole, enilconazole, epoxiconazole,
fluquinconazole, fenbuconazole, flusilazole, flutriafol, hexaconazole,
imibenconazole, ipconazole, metconazole, myclobutanil,
penconazole, propiconazole, prothioconazole, simeconazole, triadi-
mefon, triadimenol, tebuconazole, tetraconazole, triticonazole;
prochloraz, pefurazoate, imazalil, triflumizole, cyazofamid;
benomyl, carbendazim, thiabendazole, fuberidazole;
ethaboxam, etridiazole, hymexazole;
B) strobilurins, such as azoxystrobin, dimoxystrobin, enestroburin,
fluoxastrobin, kresoxim-methyl, metominostrobin, orysastrobin,
picoxystrobin, pyraclostrobin, trifloxystrobin, or methyl (2-chloro-5-[1-
(3-methylbenzyloxyimino)ethyl]benzyl)carbamate, methyl (2-chloro-5-
[1-(6-methylpyridin-2-ylmethoxyimino)ethyl]benzyl)carbamate, methyl
2-(ortho-((2,5-dimethylphenyloxymethylene)phenyl)-3-methoxyacryl-
ate;
C) carboxamides, such as carboxin, benalaxyl, boscalid, fenhexamid,
flutolanil, furametpyr, mepronil, metalaxyl, mefenoxam, ofurace,
oxadixyl,
oxycarboxin, penthiopyrad, thifluzamide, tiadinil, N-(4'-bromobiphenyl-
2-yl)-4-difluoromethyl-2-methylthiazole-5-carboxamide, N-(4'-
trifluoromethylbiphenyl-2-yl)-4-difluoromethyl-2-methylthiazole-5-
carboxamide, N-(4'-chloro-3'-fluorobiphenyl-2-yl)-4-difluoromethyl-2-
methylthiazole-5-carboxamide, N-(3',4'-dichloro-4-fluorobiphenyl-2-
yl)-3-difluoromethyl-1 -methylpyrazole-4-carboxamide, N-(3',4'-
dichloro-5-fluorobiphenyl-2-yl)-3-difluoromethyl-1-methylpyrazole-4-
carboxamide;
3,4-dichloro-N-(2-cyanophenyl)isothiazol-5-carboxamide;
dimethomorph, flumorph;
fiumetover, fluopicolide (picobenzamid), zoxamide;
carpropamid, diclocymet, mandipropamid;
N-(2-{4-[3-(4-chlorophenyl)prop-2-ynyloxy]-3-methoxyphenyl}ethyl)-2-
methanesulfonylamino-3-methylbutyramide, N-(2-{4-[3-(4-
chlorophenyl)-prop-2-ynyloxy]-3-methoxyphenyl}ethyl)-2-ethan-
esulfonylamino-3-methyl-butyramide;
D) heterocylic compounds, selected from fluazinam, pyrifenox;
bupirimate, cyprodinil, fenarimol, ferimzone, mepanipyrim, nuarimol,

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52
pyrimethanil;
triforine;
fenpiclonil, fludioxonil;
aldimorph, dodemorph, fenpropimorph, tridemorph; fenpropidin,
iprodione, procymidone, vinclozolin;
famoxadone, fenamidone, octhilinone, probenazole;
anilazine, diclomezine, pyroquilon, proquinazid, tricyclazole;
amisulbrom;
5-chloro-7-(4-methylpiperidin-1-yl)-6-(2,4,6-trifluorophenyl)-[1,2,4]tri-
azolo[1,5-a]pyrimidine, 2-butoxy-6-iodo-3-propylchromen-4-one;
acibenzolar-S-methyl, captafol, captan, dazomet, folpet, fenoxanil,
quinoxyfen; 3-[5-(4-chlorophenyl)-2,3-dimethylisoxazolidin-3-
yl]pyridine;
E) carbamates, such as mancozeb, maneb, metam, metiram, ferbam,
propineb, thiram, zineb, ziram;
diethofencarb, iprovalicarb, flubenthiavalicarb, propamocarb;
methyl 3-(4-chlorophenyl)-3-(2-isopropoxycarbonylamino-3-methyl-
butyrylamino)propanoate;
and
F) other active compounds, selected from the group consisting of
guanidines: dodine, iminoctadine, guazatine;
antibiotics: kasugamycin, streptomycin, polyoxine, validamycin A;
nitrophenyl derivates: binapacryl, dinocap, dinobuton;
sulfur-containing heterocyclyl compounds: dithianon, isoprothiolane;
organometal compounds: fentin salts, such as fentin-acetate;
organophosphorus compounds: edifenphos, iprobenfos, fosetyl,
fosetyl-aluminum, phosphorous acid and its salts, pyrazophos,
tolclofos-methyl;
organochlorine compounds: chlorothalonil, dichlofluanid, flusulfamide,
hexachlorobenzene, phthalide, pencycuron, quintozene, thiophanate-
methyl, tolylfluanid;
inorganic active compounds: Bordeaux mixture, copper acetate,
copper hydroxide, copper oxychloride, basic copper sulfate, sulfur;
others: cyflufenamid, cymoxanil, dimethirimol, ethirimol, furalaxyl,
metrafenone and spiroxamine;
growth retardants: prohexadione and its salts, trinexapac-ethyl,
chlormequat, mepiquat-chloride and diflufenzopyr;
in a synergistically effective amount.

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2. The fungicidal mixture according to claim 1, comprising a compound of the
formula I and a compound of the formula II in a weight ratio of from 100:1 to
1:100.
3. The fungicidal mixture according to claim 1 or 2, comprising a compound of the
formula I corresponding to the formula IA

in which
R1 is C3-C-12-alkyl, C5-C12-alkoxyalkyl, phenyl or phenyl-C1-C4-alkyl, where
phenyl may be substituted by one to three groups Rb;
R2 is C1-C12-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy-C1-C4-alkyl;
R3 is hydrogen or NH2.
4. The fungicidal mixture according to any of claims 1 to 3, comprising as
component 1 a compound selected from the group consisting of 6-(3,4-dichloro-
phenyl)-5-methyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine, 6-(4-tert-butylphenyl)-
5-methyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine, 5-methyl-6-(3,5,5-trimethyl-
hexyl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine, 5-methyl-6-octyl-
[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine, 6-methyl-5-octyl-[1,2,4]triazolo[1,5-
a]pyrimidin-7-ylamine, 6-ethyl-5-octyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine, 5-
ethyl-6-octyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine, 5-ethyl-6-(3,5,5-trimethyl-
hexyl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine, 6-octyl-5-propyl-
[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine, 5-methoxymethyl-6-octyl-
[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine, 6-octyl-5-trifluormethyl-
[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine and 5-trifluoromethyl-6-(3,5,5~trimethyl-
hexyl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine.
5. The fungicida! mixture according to any of claims 1 to 4, comprising as
component 2 an active compound II selected from the groups of the azoles,
carbamates and carboxamides according to claim 1.
6. The fungicidal mixture according to any of claims 1 to 4, comprising as
component 2 an active compound II selected from the groups of the strobilurins,
heterocyclic compounds or other active compounds according to claim 1.
7. A ternary fungicidal mixture according to any of claims 1 to 6, comprising two

PF 56951
54
active compounds II.
8. A composition, comprising a liquid or solid carrier and a mixture according to any
of claims 1 to 7.
9. A method for controlling phytopathogenic harmful fungi, wherein the fungi their
habitat or the plants to be protected against fungal attack, the soil or seed are
treated with an effective amount of a compound I and at least one compound II
according to claim 1.
10. The method according to claim 9, wherein the compounds I and II according to
claim 1 are applied simultaneously, that is jointly or separately, or in succession,
11. The method according to claim 9 or 10, wherein the compounds I and II
according to claim 1 or the mixture according to any of claims 1 to 4 are/is
applied in an amount of from 5 g/ha to 2000 g/ha.
12. The method according to claim 9 or 10, wherein the compounds I and II
according to claim 1 or the mixture according to any of claims 1 to 7 are/is
applied in an amount of from 1 to 1000 g/100 kg of seed.
13. The method according to any of claims 9 to 12, wherein harmful fungi from the
class of the Oomycetes are controlled.
14. Seed, comprising a mixture according to any of claims 1 to 7 in an amount of
from 1 to 1000 g/100 kg.
15. A process for preparing a composition according to claim 8 by extending the
compounds I and II according to claim 1 with liquid or solid carriers.

Fungicidal mixtures comprising, as active components,
1) azolopyrimidinylamines of the formula I,
in which the substituents are as defined in the description and
2) at least one active compound II selected from the following groups:
azoles, strobilurins, carboxamides, heterocylic compounds, carbamates and other active compounds selected from the group consisting of guanidines,
antibiotics, sulfur-containing heterocyclyl compounds, organophosphorus compounds, organochlorine compounds, inorganic active compounds, growth retardants and cyflufenamid, cymoxanil, dimethirimol, ethirimol, furalaxyl,
metrafenone and spiroxamine;
in a synergistically effective amount.
Methods for controlling harmful fungi using mixtures of the compound I with active
compounds II and the use of the compound I with active compounds II for preparing such mixtures, and also compositions comprising these mixtures.

Documents:

00212-kolnp-2008-abstract.pdf

00212-kolnp-2008-claims.pdf

00212-kolnp-2008-correspondence others.pdf

00212-kolnp-2008-description complete.pdf

00212-kolnp-2008-form 1.pdf

00212-kolnp-2008-form 3.pdf

00212-kolnp-2008-form 5.pdf

00212-kolnp-2008-international publication.pdf

00212-kolnp-2008-international search report.pdf

00212-kolnp-2008-pct priority document notification.pdf

00212-kolnp-2008-pct request form.pdf

00212-kolnp-2008-translated copy of priority document.pdf

212-KOLNP-2008-(20-06-2012)-CORRESPONDENCE.pdf

212-KOLNP-2008-(20-06-2012)-FORM-3.pdf

212-KOLNP-2008-(26-03-2012)-ABSTRACT.pdf

212-KOLNP-2008-(26-03-2012)-AMANDED CLAIMS.pdf

212-KOLNP-2008-(26-03-2012)-DESCRIPTION (COMPLETE).pdf

212-KOLNP-2008-(26-03-2012)-EXAMINATION REPORT REPLY RECEIVED.pdf

212-KOLNP-2008-(26-03-2012)-FORM-1.pdf

212-KOLNP-2008-(26-03-2012)-FORM-2.pdf

212-KOLNP-2008-(26-03-2012)-FORM-3.pdf

212-KOLNP-2008-(26-03-2012)-IPRB.pdf

212-KOLNP-2008-(26-03-2012)-OTHERS.pdf

212-KOLNP-2008-(26-03-2012)-PA-CERTIFIED COPIES.pdf

212-KOLNP-2008-(26-03-2012)-PETITION UNDER RULE 137.pdf

212-KOLNP-2008-ASSIGNMENT.pdf

212-KOLNP-2008-CORRESPONDENCE OTHERS 1.1.pdf

212-KOLNP-2008-CORRESPONDENCE.pdf

212-KOLNP-2008-EXAMINATION REPORT.pdf

212-kolnp-2008-form 18.pdf

212-KOLNP-2008-FORM 3.pdf

212-KOLNP-2008-FORM 5.pdf

212-KOLNP-2008-GPA.pdf

212-KOLNP-2008-GRANTED-ABSTRACT.pdf

212-KOLNP-2008-GRANTED-CLAIMS.pdf

212-KOLNP-2008-GRANTED-DESCRIPTION (COMPLETE).pdf

212-KOLNP-2008-GRANTED-FORM 1.pdf

212-KOLNP-2008-GRANTED-FORM 2.pdf

212-KOLNP-2008-GRANTED-SPECIFICATION.pdf

212-KOLNP-2008-OTHERS.pdf

212-KOLNP-2008-REPLY TO EXAMINATION REPORT.pdf

212-KOLNP-2008-TRANSLATED COPY OF PRIORITY DOCUMENT.pdf

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Patent Number

254295

Indian Patent Application Number

212/KOLNP/2008

PG Journal Number

42/2012

Publication Date

19-Oct-2012

Grant Date

17-Oct-2012

Date of Filing

15-Jan-2008

Name of Patentee

BASF AKTIENGESELLSCHAFT

Applicant Address

67056 LUDWIGSHAFEN

Inventors:

#	Inventor's Name	Inventor's Address
1	BECK CHRISTINE	RHEINDAMMSTR 25, 68163 MANNHEIM
2	SCHERER MARIA	HERMANN-JURGENS-STR 30, 76829 LANDAU
3	STIERL REINHARD	JAHNSTR 8, 67251 FREINSHEIM
4	STRATHMANN SIEGFRIED	DONNERSBERGSTR 9, 67117 LIMBURGERHOF
5	HUNGER UDO	UHLANDSTR 14, 68167 MANNHEIM
6	NIEDENBRUCK MATTHIAS	ALBERT-EINSTEIN-ALLEE 3, 67117 LIMBURGERHOF

PCT International Classification Number

A01N 43/90,A01P 3/00

PCT International Application Number

PCT/EP2006/064463

PCT International Filing date

2006-07-20

PCT Conventions:

#	PCT Application Number	Date of Convention	Priority Country
1	102005035688.5	2005-07-27	Germany