UA78255C2 - 5-phenylpyrimidines, method of production thereof (variants), fungicidal agent containing thereof - Google Patents

5-phenylpyrimidines, method of production thereof (variants), fungicidal agent containing thereof Download PDF

Info

Publication number: UA78255C2
Authority: UA; Ukraine
Prior art keywords: formula; chloro; alkyl; haloalkyl; compounds
Prior art date: 2001-11-19

Application number

UA20040604823A

Other languages

English (en)

Ukrainian (uk)

Original Assignee

Basf Ag

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2001-11-19

Filing date

2002-11-15

Publication date

2007-03-15

2002-11-15 Application filed by Basf Ag filed Critical Basf Ag

2007-03-15 Publication of UA78255C2 publication Critical patent/UA78255C2/uk

Links

238000000034 method Methods 0.000 title claims abstract description 11
LVXOXXGCJHYEOS-UHFFFAOYSA-N 5-phenylpyrimidine Chemical class C1=CC=CC=C1C1=CN=CN=C1 LVXOXXGCJHYEOS-UHFFFAOYSA-N 0.000 title claims abstract description 5
238000004519 manufacturing process Methods 0.000 title claims abstract description 4
239000000417 fungicide Substances 0.000 title claims description 13
-1 sulphoxy Chemical group 0.000 claims abstract description 180
150000001875 compounds Chemical class 0.000 claims abstract description 102
125000004433 nitrogen atom Chemical group N* 0.000 claims abstract description 18
125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 15
125000001188 haloalkyl group Chemical group 0.000 claims abstract description 14
229920006395 saturated elastomer Polymers 0.000 claims abstract description 11
125000005843 halogen group Chemical group 0.000 claims abstract description 9
125000001424 substituent group Chemical group 0.000 claims abstract description 9
229910052757 nitrogen Inorganic materials 0.000 claims abstract description 8
125000000852 azido group Chemical group *N=[N+]=[N-] 0.000 claims abstract description 7
125000003342 alkenyl group Chemical group 0.000 claims abstract description 5
239000003795 chemical substances by application Substances 0.000 claims abstract description 4
125000004438 haloalkoxy group Chemical group 0.000 claims abstract 3
239000001257 hydrogen Substances 0.000 claims description 29
229910052739 hydrogen Inorganic materials 0.000 claims description 29
230000003993 interaction Effects 0.000 claims description 22
229910052736 halogen Inorganic materials 0.000 claims description 20
150000002367 halogens Chemical class 0.000 claims description 20
229910052740 iodine Inorganic materials 0.000 claims description 20
150000002431 hydrogen Chemical class 0.000 claims description 18
150000003457 sulfones Chemical class 0.000 claims description 14
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 13
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 12
241000233866 Fungi Species 0.000 claims description 11
238000006243 chemical reaction Methods 0.000 claims description 10
239000000460 chlorine Substances 0.000 claims description 9
229910052801 chlorine Inorganic materials 0.000 claims description 9
239000000463 material Substances 0.000 claims description 9
230000003032 phytopathogenic effect Effects 0.000 claims description 9
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 8
125000004122 cyclic group Chemical group 0.000 claims description 8
125000001072 heteroaryl group Chemical group 0.000 claims description 8
125000004430 oxygen atom Chemical group O* 0.000 claims description 8
125000005842 heteroatom Chemical group 0.000 claims description 7
125000000623 heterocyclic group Chemical group 0.000 claims description 7
229910052760 oxygen Inorganic materials 0.000 claims description 7
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 6
150000001412 amines Chemical class 0.000 claims description 6
125000004682 aminothiocarbonyl group Chemical group NC(=S)* 0.000 claims description 6
239000007787 solid Substances 0.000 claims description 6
125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims description 5
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 4
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 4
229910052794 bromium Inorganic materials 0.000 claims description 4
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 4
125000004450 alkenylene group Chemical group 0.000 claims description 3
125000002947 alkylene group Chemical group 0.000 claims description 3
125000000304 alkynyl group Chemical group 0.000 claims description 3
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 3
150000003230 pyrimidines Chemical class 0.000 claims description 3
239000002689 soil Substances 0.000 claims description 3
150000001409 amidines Chemical class 0.000 claims description 2
125000004429 atom Chemical group 0.000 claims description 2
150000002148 esters Chemical class 0.000 claims description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
150000002902 organometallic compounds Chemical class 0.000 claims description 2
DUFGYCAXVIUXIP-UHFFFAOYSA-N 4,6-dihydroxypyrimidine Chemical class OC1=CC(O)=NC=N1 DUFGYCAXVIUXIP-UHFFFAOYSA-N 0.000 claims 1
MYLBTCQBKAKUTJ-UHFFFAOYSA-N 7-methyl-6,8-bis(methylsulfanyl)pyrrolo[1,2-a]pyrazine Chemical compound C1=CN=CC2=C(SC)C(C)=C(SC)N21 MYLBTCQBKAKUTJ-UHFFFAOYSA-N 0.000 claims 1
230000026030 halogenation Effects 0.000 claims 1
238000005658 halogenation reaction Methods 0.000 claims 1
239000007788 liquid Substances 0.000 claims 1
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
238000012876 topography Methods 0.000 claims 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract description 24
125000000217 alkyl group Chemical group 0.000 abstract description 12
125000003545 alkoxy group Chemical group 0.000 abstract description 5
125000003302 alkenyloxy group Chemical group 0.000 abstract description 3
125000004414 alkyl thio group Chemical group 0.000 abstract description 2
125000000753 cycloalkyl group Chemical group 0.000 abstract description 2
125000000262 haloalkenyl group Chemical group 0.000 abstract description 2
229910003827 NRaRb Inorganic materials 0.000 abstract 3
125000006193 alkinyl group Chemical group 0.000 abstract 2
208000031888 Mycoses Diseases 0.000 abstract 1
125000005108 alkenylthio group Chemical group 0.000 abstract 1
125000004995 haloalkylthio group Chemical group 0.000 abstract 1
125000005347 halocycloalkyl group Chemical group 0.000 abstract 1
230000001473 noxious effect Effects 0.000 abstract 1
125000000446 sulfanediyl group Chemical group *S* 0.000 abstract 1
239000013543 active substance Substances 0.000 description 38
239000003921 oil Substances 0.000 description 27
239000002245 particle Substances 0.000 description 25
241000196324 Embryophyta Species 0.000 description 22
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 20
229910052784 alkaline earth metal Inorganic materials 0.000 description 18
239000002904 solvent Substances 0.000 description 18
238000002360 preparation method Methods 0.000 description 17
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 17
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 16
239000000203 mixture Substances 0.000 description 16
239000000243 solution Substances 0.000 description 16
125000004432 carbon atom Chemical group C* 0.000 description 14
241000894007 species Species 0.000 description 14
BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 13
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 12
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 12
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 11
239000003513 alkali Substances 0.000 description 11
150000001342 alkaline earth metals Chemical class 0.000 description 11
239000002585 base Substances 0.000 description 11
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 11
239000000047 product Substances 0.000 description 11
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 10
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 10
239000000741 silica gel Substances 0.000 description 10
229910002027 silica gel Inorganic materials 0.000 description 10
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 9
150000003839 salts Chemical class 0.000 description 9
235000013339 cereals Nutrition 0.000 description 8
239000003995 emulsifying agent Substances 0.000 description 8
229910052717 sulfur Inorganic materials 0.000 description 8
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 7
KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 7
239000006185 dispersion Substances 0.000 description 7
150000002430 hydrocarbons Chemical group 0.000 description 7
239000011541 reaction mixture Substances 0.000 description 7
240000008067 Cucumis sativus Species 0.000 description 6
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 6
WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 6
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
238000010410 dusting Methods 0.000 description 6
239000000839 emulsion Substances 0.000 description 6
239000000945 filler Substances 0.000 description 6
229910052731 fluorine Inorganic materials 0.000 description 6
239000011737 fluorine Substances 0.000 description 6
230000003902 lesion Effects 0.000 description 6
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
239000000843 powder Substances 0.000 description 6
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 6
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 5
240000005979 Hordeum vulgare Species 0.000 description 5
235000007340 Hordeum vulgare Nutrition 0.000 description 5
239000002253 acid Substances 0.000 description 5
230000015572 biosynthetic process Effects 0.000 description 5
239000004359 castor oil Substances 0.000 description 5
235000019438 castor oil Nutrition 0.000 description 5
238000004587 chromatography analysis Methods 0.000 description 5
239000002270 dispersing agent Substances 0.000 description 5
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 5
239000001301 oxygen Substances 0.000 description 5
239000006072 paste Substances 0.000 description 5
238000005507 spraying Methods 0.000 description 5
125000004434 sulfur atom Chemical group 0.000 description 5
OXPDQFOKSZYEMJ-UHFFFAOYSA-N 2-phenylpyrimidine Chemical class C1=CC=CC=C1C1=NC=CC=N1 OXPDQFOKSZYEMJ-UHFFFAOYSA-N 0.000 description 4
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
235000009849 Cucumis sativus Nutrition 0.000 description 4
ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 4
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
241000221785 Erysiphales Species 0.000 description 4
235000007688 Lycopersicon esculentum Nutrition 0.000 description 4
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
240000007594 Oryza sativa Species 0.000 description 4
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LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 4
241000209140 Triticum Species 0.000 description 4
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150000001298 alcohols Chemical class 0.000 description 4
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125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 description 2
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CSDQQAQKBAQLLE-UHFFFAOYSA-N 4-(4-chlorophenyl)-4,5,6,7-tetrahydrothieno[3,2-c]pyridine Chemical compound C1=CC(Cl)=CC=C1C1C(C=CS2)=C2CCN1 CSDQQAQKBAQLLE-UHFFFAOYSA-N 0.000 description 2
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229910052703 rhodium Inorganic materials 0.000 description 1
239000010948 rhodium Substances 0.000 description 1
MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
WWYDYZMNFQIYPT-UHFFFAOYSA-N ru78191 Chemical compound OC(=O)C(C(O)=O)C1=CC=CC=C1 WWYDYZMNFQIYPT-UHFFFAOYSA-N 0.000 description 1
229930195734 saturated hydrocarbon Chemical group 0.000 description 1
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
125000003548 sec-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
125000005624 silicic acid group Chemical class 0.000 description 1
RMBAVIFYHOYIFM-UHFFFAOYSA-M sodium methanethiolate Chemical compound [Na+].[S-]C RMBAVIFYHOYIFM-UHFFFAOYSA-M 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
239000007921 spray Substances 0.000 description 1
235000021012 strawberries Nutrition 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
150000003462 sulfoxides Chemical class 0.000 description 1
125000004962 sulfoxyl group Chemical group 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
239000002641 tar oil Substances 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
210000001550 testis Anatomy 0.000 description 1
PCZOZSATUTWXIC-UHFFFAOYSA-N tetraethylazanium;cyanide Chemical compound N#[C-].CC[N+](CC)(CC)CC PCZOZSATUTWXIC-UHFFFAOYSA-N 0.000 description 1
150000005326 tetrahydropyrimidines Chemical class 0.000 description 1
CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical compound COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 description 1
KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical class CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1
238000009827 uniform distribution Methods 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
239000003981 vehicle Substances 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
239000002023 wood Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/47—One nitrogen atom and one oxygen or sulfur atom, e.g. cytosine
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/48—Two nitrogen atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/52—Two oxygen atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Plural Heterocyclic Compounds (AREA)

UA20040604823A 2001-11-19 2002-11-15 5-phenylpyrimidines, method of production thereof (variants), fungicidal agent containing thereof UA78255C2 (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE10156279		2001-11-19
PCT/EP2002/012807 WO2003043993A1 (fr)	2001-11-19	2002-11-15	5-phenylpyrimidines, procede pour les produire, agents les contenant et leur utilisation

Publications (1)

Publication Number	Publication Date
UA78255C2 true UA78255C2 (en)	2007-03-15

Family

ID=7705956

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
UA20040604823A UA78255C2 (en)	2001-11-19	2002-11-15	5-phenylpyrimidines, method of production thereof (variants), fungicidal agent containing thereof

Country Status (17)

Country	Link
US (2)	US7465735B2 (fr)
EP (1)	EP1448532A1 (fr)
JP (1)	JP4450625B2 (fr)
KR (1)	KR100950632B1 (fr)
CN (1)	CN1312134C (fr)
AU (1)	AU2002352015B2 (fr)
BR (1)	BR0214253A (fr)
CA (1)	CA2467683C (fr)
EA (1)	EA010628B1 (fr)
HU (1)	HUP0402385A3 (fr)
IL (1)	IL161893A0 (fr)
MX (1)	MXPA04004583A (fr)
NZ (1)	NZ533265A (fr)
PL (1)	PL371059A1 (fr)
UA (1)	UA78255C2 (fr)
WO (1)	WO2003043993A1 (fr)
ZA (1)	ZA200404835B (fr)

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CN100453535C (zh) *	2003-05-20	2009-01-21	巴斯福股份公司	2-取代嘧啶
JP2006528603A (ja) *	2003-07-24	2006-12-21	ビーエーエスエフ　アクチェンゲゼルシャフト	２−置換ピリミジン
CN1826327A (zh) *	2003-07-24	2006-08-30	巴斯福股份公司	2－取代的嘧啶
RU2006107578A (ru)	2003-09-24	2007-10-27	Вайет Холдингз Корпорейшн (Us)	6-арилпиримидин, применяемый в качестве противоракового агента
JP2005232081A (ja) *	2004-02-19	2005-09-02	Bayer Cropscience Ag	ベンジルピリミジン誘導体の農園芸用殺菌剤としての利用
CN1956974B (zh)	2004-05-19	2010-11-24	巴斯福股份公司	2-取代嘧啶及其作为农药的用途
BRPI0512306A (pt) *	2004-06-25	2008-02-26	Basf Ag	compostos, processo para a preparação dos mesmos, agente pesticida, e, processos para o combate de fungos nocivos fitopatogênicos e de pragas de animais em agricultura
WO2006005571A1 (fr) *	2004-07-14	2006-01-19	Basf Aktiengesellschaft	Pyrimidines substituees en position 2, procedes de production de ces composes et leur utilisation pour lutter contre des champignons nuisibles
TW200637556A (en) *	2005-01-31	2006-11-01	Basf Ag	Substituted 5-phenyl pyrimidines I in therapy
TW200640881A (en) *	2005-02-15	2006-12-01	Du Pont	Fungicidal pyrazine derivatives
DE102005046592A1 (de) *	2005-09-28	2007-03-29	Basf Ag	2-Substituierte Hydroxylaminopyrimidine, Verfahren zu ihrer Herstellung und ihre Verwendung als Pestizid
WO2007054472A1 (fr) *	2005-11-11	2007-05-18	Basf Se	Derive de pyridine et de pyrimidine, leur procede de fabrication et leur utilisation en tant que pesticides
CN101384562A (zh) *	2006-02-15	2009-03-11	巴斯夫欧洲公司	2-取代的嘧啶及其作为农药的用途
WO2007110418A2 (fr) *	2006-03-27	2007-10-04	Basf Se	5-hetaryl-4-aminopyrimidines substituees
CL2007002231A1 (es) *	2006-08-02	2008-04-11	Basf Ag	Uso de compuestos derivados de 5-(het) arilpirimidina para combatir hongos daninos; compuestos derivados de 5-(het) arilpirimidina; agente fungicida; y agente farmaceutico.
WO2008107398A2 (fr) *	2007-03-02	2008-09-12	Basf Se	Composés de pyrazine
KR20100137573A (ko) *	2008-04-22	2010-12-30	바이엘 크롭사이언스 아게	살진균제 히드록시모일-헤테로시클 유도체
CA2787488A1 (fr)	2009-12-17	2011-07-14	Dow Agrosciences Llc	Derives de 2-aldoximino-5-fluoropyrimidine
WO2011156174A1 (fr)	2010-06-07	2011-12-15	Dow Agrosciences Llc	Pyrazinyl-carboxamides utilisés comme fongicides
US9321735B2 (en) *	2010-07-20	2016-04-26	Vestaron Corporation	Insecticidal triazines and pyrimidines

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US3919229A (en) *	1973-07-19	1975-11-11	Labaz	Pyrimidine derivatives and process for preparing the same
DE3620841A1 (de) *	1986-06-21	1987-12-23	Basf Ag	4-aminopyrimidinderivate
DE3901084A1 (de)	1988-07-28	1990-02-01	Bayer Ag	Substituierte 4-sulfonylamino-2-azinyl-1,2,4-triazol-3-one, verfahren sowie zwischenprodukte zu ihrer herstellung und ihre verwendung als herbizide
FI895821A7 (fi) *	1988-12-07	1990-06-08	The Wellcome Foundation Ltd	Farmaseuttisesti aktivisia CNS-yhdisteitä
JPH02200678A (ja) *	1989-01-28	1990-08-08	Kumiai Chem Ind Co Ltd	２―ヨードプロパルギルオキシピリミジン誘導体及び農園芸用殺菌剤
DE3922735A1 (de)	1989-07-11	1991-01-24	Hoechst Ag	Aminopyrimidin-derivate, verfahren zu ihrer herstellung, sie enthaltende mittel und ihre verwendung als fungizide
WO1992010490A1 (fr)	1990-12-05	1992-06-25	Hoechst Aktiengesellschaft	Derives de pyridyle-pyrimidine, leur procede de production, agents les contenant et leur utilisation comme fongicides
DE4227811A1 (de)	1992-08-21	1994-02-24	Hoechst Ag	2-Pyridyl-pyrimidin-Derivate, Verfahren zu ihrer Herstellung, sie enthaltende Mittel und ihre Verwendung als Fungizide
GB2277090A (en)	1993-04-16	1994-10-19	Shell Int Research	Fungicidal tetrahydropyrimidine and imidazoline derivatives
US6440965B1 (en) *	1997-10-15	2002-08-27	Krenitsky Pharmaceuticals, Inc.	Substituted pyrimidine derivatives, their preparation and their use in the treatment of neurodegenerative or neurological disorders of the central nervous system
JP2004503542A (ja) *	2000-06-13	2004-02-05	ビーエーエスエフ　アクチェンゲゼルシャフト	殺真菌性５−フェニル置換２−（シアノアミノ）ピリミジン誘導体
EA007719B1 (ru) *	2001-03-15	2006-12-29	Басф Акциенгезельшафт	5-фенилпиримидины, способ и промежуточные продукты для их получения и их применение для борьбы с фитопатогенными грибами

2002
- 2002-11-15 NZ NZ533265A patent/NZ533265A/en not_active IP Right Cessation
- 2002-11-15 KR KR1020047007560A patent/KR100950632B1/ko not_active Expired - Fee Related
- 2002-11-15 HU HU0402385A patent/HUP0402385A3/hu unknown
- 2002-11-15 EA EA200400597A patent/EA010628B1/ru not_active IP Right Cessation
- 2002-11-15 WO PCT/EP2002/012807 patent/WO2003043993A1/fr not_active Ceased
- 2002-11-15 JP JP2003545630A patent/JP4450625B2/ja not_active Expired - Fee Related
- 2002-11-15 CN CNB028255356A patent/CN1312134C/zh not_active Expired - Fee Related
- 2002-11-15 PL PL02371059A patent/PL371059A1/xx not_active Application Discontinuation
- 2002-11-15 US US10/495,280 patent/US7465735B2/en not_active Expired - Fee Related
- 2002-11-15 UA UA20040604823A patent/UA78255C2/uk unknown
- 2002-11-15 EP EP02787691A patent/EP1448532A1/fr not_active Withdrawn
- 2002-11-15 MX MXPA04004583A patent/MXPA04004583A/es active IP Right Grant
- 2002-11-15 BR BR0214253-8A patent/BR0214253A/pt not_active Application Discontinuation
- 2002-11-15 AU AU2002352015A patent/AU2002352015B2/en not_active Ceased
- 2002-11-15 IL IL16189302A patent/IL161893A0/xx unknown
- 2002-11-15 CA CA2467683A patent/CA2467683C/fr not_active Expired - Fee Related
2004
- 2004-06-18 ZA ZA200404835A patent/ZA200404835B/en unknown
2007
- 2007-02-22 US US11/677,862 patent/US7449471B2/en not_active Expired - Fee Related

Also Published As

Publication number	Publication date
CN1312134C (zh)	2007-04-25
AU2002352015B2 (en)	2008-07-31
CN1606547A (zh)	2005-04-13
HUP0402385A2 (hu)	2005-03-29
US20060148764A1 (en)	2006-07-06
PL371059A1 (en)	2005-06-13
HUP0402385A3 (en)	2005-10-28
WO2003043993A1 (fr)	2003-05-30
MXPA04004583A (es)	2004-08-13
US7465735B2 (en)	2008-12-16
IL161893A0 (en)	2005-11-20
JP4450625B2 (ja)	2010-04-14
US7449471B2 (en)	2008-11-11
CA2467683C (fr)	2011-09-27
EP1448532A1 (fr)	2004-08-25
ZA200404835B (en)	2005-06-20
EA010628B1 (ru)	2008-10-30
CA2467683A1 (fr)	2003-05-30
NZ533265A (en)	2006-05-26
EA200400597A1 (ru)	2004-12-30
BR0214253A (pt)	2004-12-14
KR20040079901A (ko)	2004-09-16
KR100950632B1 (ko)	2010-04-01
US20070149551A1 (en)	2007-06-28
AU2002352015A1 (en)	2003-06-10
JP2005514363A (ja)	2005-05-19

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JP2007502846A (ja)	2007-02-15	２−置換ピリミジン類
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