ZA200600209B - Pyridinylanilides - Google Patents
Pyridinylanilides Download PDFInfo
- Publication number
- ZA200600209B ZA200600209B ZA200600209A ZA200600209A ZA200600209B ZA 200600209 B ZA200600209 B ZA 200600209B ZA 200600209 A ZA200600209 A ZA 200600209A ZA 200600209 A ZA200600209 A ZA 200600209A ZA 200600209 B ZA200600209 B ZA 200600209B
- Authority
- ZA
- South Africa
- Prior art keywords
- alkyl
- case
- halogenoalkyl
- formula
- chlorine
- Prior art date
Links
- -1 cyano, nitro, amino, hydroxyl Chemical group 0.000 claims description 194
- 239000001257 hydrogen Substances 0.000 claims description 154
- 229910052739 hydrogen Inorganic materials 0.000 claims description 154
- 150000002431 hydrogen Chemical group 0.000 claims description 118
- 229910052799 carbon Inorganic materials 0.000 claims description 115
- 125000004432 carbon atom Chemical group C* 0.000 claims description 114
- 229910052736 halogen Inorganic materials 0.000 claims description 112
- 150000002367 halogens Chemical class 0.000 claims description 112
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical group [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims description 107
- 150000003254 radicals Chemical class 0.000 claims description 87
- 239000000460 chlorine Chemical group 0.000 claims description 86
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 85
- 229910052801 chlorine Inorganic materials 0.000 claims description 85
- 125000005843 halogen group Chemical group 0.000 claims description 83
- 229910052731 fluorine Inorganic materials 0.000 claims description 81
- 239000011737 fluorine Chemical group 0.000 claims description 81
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 65
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 60
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 56
- 229910052794 bromium Inorganic materials 0.000 claims description 56
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 55
- 125000001246 bromo group Chemical group Br* 0.000 claims description 55
- 125000000217 alkyl group Chemical group 0.000 claims description 50
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 39
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 38
- 125000000623 heterocyclic group Chemical group 0.000 claims description 34
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 30
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 28
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 27
- 150000002430 hydrocarbons Chemical group 0.000 claims description 26
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 20
- 125000001188 haloalkyl group Chemical group 0.000 claims description 19
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 17
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 15
- 125000004438 haloalkoxy group Chemical group 0.000 claims description 15
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 15
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 14
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 14
- 125000003545 alkoxy group Chemical group 0.000 claims description 14
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 14
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims description 14
- 125000003282 alkyl amino group Chemical group 0.000 claims description 14
- 125000004414 alkyl thio group Chemical group 0.000 claims description 14
- 125000005125 aryl alkyl amino carbonyl group Chemical group 0.000 claims description 14
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 14
- 125000000000 cycloalkoxy group Chemical group 0.000 claims description 14
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 14
- 125000005202 dialkylaminocarbonyloxy group Chemical group 0.000 claims description 14
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 14
- 125000003302 alkenyloxy group Chemical group 0.000 claims description 13
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims description 13
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 claims description 13
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims description 13
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 13
- 125000006350 alkyl thio alkyl group Chemical group 0.000 claims description 13
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 13
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 13
- 239000005864 Sulphur Chemical group 0.000 claims description 12
- 125000003342 alkenyl group Chemical group 0.000 claims description 12
- 125000005090 alkenylcarbonyl group Chemical group 0.000 claims description 12
- 125000005087 alkynylcarbonyl group Chemical group 0.000 claims description 12
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 12
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 12
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 12
- 125000005188 oxoalkyl group Chemical group 0.000 claims description 12
- 125000003884 phenylalkyl group Chemical group 0.000 claims description 12
- 125000004660 phenylalkylthio group Chemical group 0.000 claims description 12
- 125000004076 pyridyl group Chemical group 0.000 claims description 12
- 150000001875 compounds Chemical class 0.000 claims description 11
- 125000004983 dialkoxyalkyl group Chemical group 0.000 claims description 11
- 125000004473 dialkylaminocarbonyl group Chemical group 0.000 claims description 11
- 125000004415 heterocyclylalkyl group Chemical group 0.000 claims description 11
- 229910052757 nitrogen Inorganic materials 0.000 claims description 11
- 239000003085 diluting agent Substances 0.000 claims description 10
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 10
- 150000001412 amines Chemical class 0.000 claims description 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 9
- WGLLSSPDPJPLOR-UHFFFAOYSA-N 2,3-dimethylbut-2-ene Chemical group CC(C)=C(C)C WGLLSSPDPJPLOR-UHFFFAOYSA-N 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 8
- 239000011230 binding agent Substances 0.000 claims description 8
- 239000003054 catalyst Substances 0.000 claims description 8
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 7
- 244000005700 microbiome Species 0.000 claims description 7
- 125000004205 trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 claims description 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 6
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 6
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 6
- 125000005842 heteroatom Chemical group 0.000 claims description 6
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 239000001301 oxygen Substances 0.000 claims description 6
- 229910052760 oxygen Inorganic materials 0.000 claims description 6
- 229920006395 saturated elastomer Polymers 0.000 claims description 6
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 4
- 125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 claims description 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 4
- 125000004043 oxo group Chemical group O=* 0.000 claims description 4
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 4
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 4
- 150000001642 boronic acid derivatives Chemical class 0.000 claims description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 3
- 125000001475 halogen functional group Chemical group 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 3
- 125000003506 n-propoxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])O* 0.000 claims description 3
- 125000004429 atom Chemical group 0.000 claims description 2
- IPWKHHSGDUIRAH-UHFFFAOYSA-N bis(pinacolato)diboron Chemical compound O1C(C)(C)C(C)(C)OB1B1OC(C)(C)C(C)(C)O1 IPWKHHSGDUIRAH-UHFFFAOYSA-N 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 125000004786 difluoromethoxy group Chemical group [H]C(F)(F)O* 0.000 claims description 2
- 125000002510 isobutoxy group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])O* 0.000 claims description 2
- 125000006606 n-butoxy group Chemical group 0.000 claims description 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 2
- 229910052763 palladium Inorganic materials 0.000 claims description 2
- 229910052697 platinum Inorganic materials 0.000 claims description 2
- 125000005920 sec-butoxy group Chemical group 0.000 claims description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 18
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 claims 17
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 claims 13
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 11
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims 8
- 125000001153 fluoro group Chemical group F* 0.000 claims 5
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical group C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims 4
- 125000005034 trifluormethylthio group Chemical group FC(S*)(F)F 0.000 claims 4
- 125000005448 ethoxyethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims 3
- 125000005745 ethoxymethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])* 0.000 claims 3
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims 3
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims 2
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 claims 2
- 239000004606 Fillers/Extenders Substances 0.000 claims 2
- 125000004772 dichloromethyl group Chemical group [H]C(Cl)(Cl)* 0.000 claims 2
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims 2
- 239000011630 iodine Substances 0.000 claims 2
- 229910052740 iodine Inorganic materials 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 2
- 239000004094 surface-active agent Substances 0.000 claims 2
- 125000004784 trichloromethoxy group Chemical group ClC(O*)(Cl)Cl 0.000 claims 2
- GRFOHUBBUMAJMM-UHFFFAOYSA-N 3-(2-aminoquinolin-3-yl)-n-cyclohexyl-n-methylpropanamide Chemical compound C=1C2=CC=CC=C2N=C(N)C=1CCC(=O)N(C)C1CCCCC1 GRFOHUBBUMAJMM-UHFFFAOYSA-N 0.000 claims 1
- 101500025412 Mus musculus Processed cyclic AMP-responsive element-binding protein 3-like protein 1 Proteins 0.000 claims 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 1
- CPPKAGUPTKIMNP-UHFFFAOYSA-N cyanogen fluoride Chemical compound FC#N CPPKAGUPTKIMNP-UHFFFAOYSA-N 0.000 claims 1
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims 1
- 125000006125 ethylsulfonyl group Chemical group 0.000 claims 1
- 125000004705 ethylthio group Chemical group C(C)S* 0.000 claims 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000006216 methylsulfinyl group Chemical group [H]C([H])([H])S(*)=O 0.000 claims 1
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims 1
- CMWTZPSULFXXJA-VIFPVBQESA-N naproxen Chemical group C1=C([C@H](C)C(O)=O)C=CC2=CC(OC)=CC=C21 CMWTZPSULFXXJA-VIFPVBQESA-N 0.000 claims 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 claims 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 claims 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 1
- BRNULMACUQOKMR-UHFFFAOYSA-N thiomorpholine Chemical group C1CSCCN1 BRNULMACUQOKMR-UHFFFAOYSA-N 0.000 claims 1
- 125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 0.000 claims 1
- 150000003931 anilides Chemical group 0.000 description 4
- PIUBETKNKYAVQX-UHFFFAOYSA-N 2-chloro-n-(2-pyridin-2-ylphenyl)pyridine-3-carboxamide Chemical compound ClC1=NC=CC=C1C(=O)NC1=CC=CC=C1C1=CC=CC=N1 PIUBETKNKYAVQX-UHFFFAOYSA-N 0.000 description 2
- 230000000855 fungicidal effect Effects 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 2
- IDVLITMJKZYNQN-UHFFFAOYSA-N 1-methyl-n-(2-pyridin-2-ylphenyl)-3-(trifluoromethyl)pyrazole-4-carboxamide Chemical compound FC(F)(F)C1=NN(C)C=C1C(=O)NC1=CC=CC=C1C1=CC=CC=N1 IDVLITMJKZYNQN-UHFFFAOYSA-N 0.000 description 1
- YHNJGNOJOLCTLO-UHFFFAOYSA-N 1-methyl-n-[2-(6-methylpyridin-2-yl)phenyl]-3-(trifluoromethyl)pyrazole-4-carboxamide Chemical compound CC1=CC=CC(C=2C(=CC=CC=2)NC(=O)C=2C(=NN(C)C=2)C(F)(F)F)=N1 YHNJGNOJOLCTLO-UHFFFAOYSA-N 0.000 description 1
- VHHVJCYUHDYAGL-UHFFFAOYSA-N 2-chloro-n-(2-pyridin-2-ylphenyl)benzamide Chemical compound ClC1=CC=CC=C1C(=O)NC1=CC=CC=C1C1=CC=CC=N1 VHHVJCYUHDYAGL-UHFFFAOYSA-N 0.000 description 1
- SIISSYWDFRBZDB-UHFFFAOYSA-N 2-chloro-n-(2-pyridin-3-ylphenyl)pyridine-3-carboxamide Chemical compound ClC1=NC=CC=C1C(=O)NC1=CC=CC=C1C1=CC=CN=C1 SIISSYWDFRBZDB-UHFFFAOYSA-N 0.000 description 1
- QCURDQJYAFTSQX-UHFFFAOYSA-N 2-chloro-n-(2-pyridin-4-ylphenyl)pyridine-3-carboxamide Chemical compound ClC1=NC=CC=C1C(=O)NC1=CC=CC=C1C1=CC=NC=C1 QCURDQJYAFTSQX-UHFFFAOYSA-N 0.000 description 1
- VORIKNMBEKFXJC-UHFFFAOYSA-N 2-methyl-n-(2-pyridin-2-ylphenyl)-4-(trifluoromethyl)-1,3-thiazole-5-carboxamide Chemical compound S1C(C)=NC(C(F)(F)F)=C1C(=O)NC1=CC=CC=C1C1=CC=CC=N1 VORIKNMBEKFXJC-UHFFFAOYSA-N 0.000 description 1
- DXRWHNNAEVBKAX-UHFFFAOYSA-N 2-methyl-n-(2-pyridin-2-ylphenyl)furan-3-carboxamide Chemical compound O1C=CC(C(=O)NC=2C(=CC=CC=2)C=2N=CC=CC=2)=C1C DXRWHNNAEVBKAX-UHFFFAOYSA-N 0.000 description 1
- FRPLIFMAVWFRPB-UHFFFAOYSA-N 2-methyl-n-[2-(6-methylpyridin-2-yl)phenyl]-4-(trifluoromethyl)-1,3-thiazole-5-carboxamide Chemical compound S1C(C)=NC(C(F)(F)F)=C1C(=O)NC1=CC=CC=C1C1=CC=CC(C)=N1 FRPLIFMAVWFRPB-UHFFFAOYSA-N 0.000 description 1
- LNGLQHMCZIPRDO-UHFFFAOYSA-N 3-chloro-n-(2-pyridin-2-ylphenyl)pyrazine-2-carboxamide Chemical compound ClC1=NC=CN=C1C(=O)NC1=CC=CC=C1C1=CC=CC=N1 LNGLQHMCZIPRDO-UHFFFAOYSA-N 0.000 description 1
- QGOCZCCPNNJXSD-UHFFFAOYSA-N 3-iodo-1-methyl-n-(2-pyridin-2-ylphenyl)pyrazole-4-carboxamide Chemical compound IC1=NN(C)C=C1C(=O)NC1=CC=CC=C1C1=CC=CC=N1 QGOCZCCPNNJXSD-UHFFFAOYSA-N 0.000 description 1
- KVMBQKFZGUTSGH-UHFFFAOYSA-N 3-methyl-n-(2-pyridin-2-ylphenyl)thiophene-2-carboxamide Chemical compound C1=CSC(C(=O)NC=2C(=CC=CC=2)C=2N=CC=CC=2)=C1C KVMBQKFZGUTSGH-UHFFFAOYSA-N 0.000 description 1
- FOIILHTZOWTLMQ-UHFFFAOYSA-N 4-iodo-n-(2-pyridin-2-ylphenyl)-1,3-thiazole-5-carboxamide Chemical compound N1=CSC(C(=O)NC=2C(=CC=CC=2)C=2N=CC=CC=2)=C1I FOIILHTZOWTLMQ-UHFFFAOYSA-N 0.000 description 1
- JUPXJINTRBKWEF-UHFFFAOYSA-N 6-methyl-n-(2-pyridin-2-ylphenyl)-2,3-dihydro-1,4-oxathiine-5-carboxamide Chemical compound S1CCOC(C)=C1C(=O)NC1=CC=CC=C1C1=CC=CC=N1 JUPXJINTRBKWEF-UHFFFAOYSA-N 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- KXDAEFPNCMNJSK-UHFFFAOYSA-N benzene carboxamide Natural products NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000003641 microbiacidal effect Effects 0.000 description 1
- PAZPNSWCAFECLL-UHFFFAOYSA-N n-(2-pyridin-2-ylphenyl)-4-(trifluoromethyl)-1,3-thiazole-5-carboxamide Chemical compound N1=CSC(C(=O)NC=2C(=CC=CC=2)C=2N=CC=CC=2)=C1C(F)(F)F PAZPNSWCAFECLL-UHFFFAOYSA-N 0.000 description 1
- WOAWQUJSUXVSKC-UHFFFAOYSA-N n-[2-(2-chloropyridin-3-yl)phenyl]-1,4-dimethylpyrrole-3-carboxamide Chemical compound CC1=CN(C)C=C1C(=O)NC1=CC=CC=C1C1=CC=CN=C1Cl WOAWQUJSUXVSKC-UHFFFAOYSA-N 0.000 description 1
- 239000005648 plant growth regulator Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/61—Halogen atoms or nitro radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D411/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms
- C07D411/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D411/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP03015733 | 2003-07-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200600209B true ZA200600209B (en) | 2007-03-28 |
Family
ID=34042832
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200600209A ZA200600209B (en) | 2003-07-10 | 2006-01-09 | Pyridinylanilides |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US20060178513A1 (de) |
| EP (1) | EP1656020A2 (de) |
| JP (1) | JP2009513514A (de) |
| KR (1) | KR20060032997A (de) |
| CN (1) | CN1845673A (de) |
| BR (1) | BRPI0412486A (de) |
| CR (1) | CR8162A (de) |
| EC (1) | ECSP066275A (de) |
| IL (1) | IL172698A0 (de) |
| MX (1) | MXPA06000267A (de) |
| WO (1) | WO2005004606A2 (de) |
| ZA (1) | ZA200600209B (de) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10354607A1 (de) | 2003-11-21 | 2005-06-16 | Bayer Cropscience Ag | Siylierte Carboxamide |
| GT200500013A (es) * | 2004-01-23 | 2005-08-10 | Amidas herbicidas | |
| DE102004005785A1 (de) | 2004-02-06 | 2005-08-25 | Bayer Cropscience Ag | 2-Halogenfuryl/thienyl-3-carboxamide |
| WO2007009717A1 (en) * | 2005-07-18 | 2007-01-25 | Syngenta Participations Ag | Pyrazole-4- carboxamide derivatives as microbiocides |
| DE102005060468A1 (de) * | 2005-12-17 | 2007-06-21 | Bayer Cropscience Ag | Thienylpyridylcarboxamide |
| WO2008053991A1 (fr) * | 2006-11-02 | 2008-05-08 | Nihon Nohyaku Co., Ltd. | Dérivé de pyrazolecarboxanilide substitué ou son sel, produit chimique agricole ou horticole, et son procédé d'utilisation |
| US8815772B2 (en) * | 2012-06-29 | 2014-08-26 | E I Du Pont De Nemours And Company | Fungicidal heterocyclic carboxamides |
| CN109071444A (zh) * | 2016-03-16 | 2018-12-21 | 拜耳作物科学股份公司 | 作为农药和植物保护剂的n-(氰苄基)-6-(环丙基-羰基氨基)-4-(苯基)-吡啶-2-羧酰胺衍生物及相关化合物 |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4194008A (en) * | 1976-09-03 | 1980-03-18 | Bayer Aktiengesellschaft | N-aryl-N'-(cyclo)-alkyl-thioureas and their use as agents for combating animal pests and plant pests |
| US5045554A (en) * | 1988-11-29 | 1991-09-03 | Monsanto Company | Substituted thiazoles and their use as fungicides |
| IL103614A (en) * | 1991-11-22 | 1998-09-24 | Basf Ag | Carboxamides for controlling botrytis and certain novel such compounds |
| US5223526A (en) * | 1991-12-06 | 1993-06-29 | Monsanto Company | Pyrazole carboxanilide fungicides and use |
| DE4231517A1 (de) * | 1992-09-21 | 1994-03-24 | Basf Ag | Carbonsäureanilide, Verfahren zu ihrer Herstellung und sie enthaltende Mittel zur Bekämpfung von Schadpilzen |
| DE4231519A1 (de) * | 1992-09-21 | 1994-03-24 | Basf Ag | Cyclohex(en)ylcarbonsäureamide, Verfahren zu ihrer Herstellung und sie enthaltende Mittel zur Bekämpfung von Schadpilzen |
| EP0722441A1 (de) * | 1993-10-06 | 1996-07-24 | E.I. Du Pont De Nemours & Company Incorporated | Herbizide heteroaryl substituierte anilide |
| JPH0892223A (ja) * | 1994-09-27 | 1996-04-09 | Mitsui Toatsu Chem Inc | ヘテロ環置換アニリン誘導体およびこれを有効成分とする農園芸用殺菌剤 |
| GB9424379D0 (en) * | 1994-12-02 | 1995-01-18 | Agrevo Uk Ltd | Fungicides |
| GB9510459D0 (en) * | 1995-05-24 | 1995-07-19 | Zeneca Ltd | Bicyclic amines |
| US5633218A (en) * | 1995-05-24 | 1997-05-27 | E. I. Du Pont De Nemours And Company | Herbicidal benzodioxoles and benzodioxanes |
| US5914344A (en) * | 1996-08-15 | 1999-06-22 | Mitsui Chemicals, Inc. | Substituted carboxanilide derivative and plant disease control agent comprising same as active ingredient |
| GB9624611D0 (en) * | 1996-11-26 | 1997-01-15 | Zeneca Ltd | Bicyclic amine compounds |
| HUP0000582A3 (en) * | 1996-11-26 | 2001-10-29 | Zeneca Ltd | Insecticidal, acaricidal and nematocidal 8-azabicyclo[3.2.1]octane-, 8-azabicyclo[3.2.1]oct-6-ene-, 9-azabicyclo[3.3.1]nonane-, 9-aza-3-oxabicyclo[3.3.1]nonane- and 9-aza-3-thiabicyclo[3.3.1]nonane derivatives, preparation and use thereof |
| GB0001447D0 (en) * | 2000-01-21 | 2000-03-08 | Novartis Ag | Organic compounds |
| GB0012671D0 (en) * | 2000-05-24 | 2000-07-19 | Merck Sharp & Dohme | Therapeutic agents |
| PL362930A1 (en) * | 2000-11-08 | 2004-11-02 | Syngenta Participations Ag | Pyrrolcarboxamides and pyrrolcarbothioamides and their agrochemical uses |
-
2004
- 2004-07-05 CN CNA2004800255772A patent/CN1845673A/zh active Pending
- 2004-07-05 EP EP04740656A patent/EP1656020A2/de not_active Ceased
- 2004-07-05 WO PCT/EP2004/007323 patent/WO2005004606A2/en active Application Filing
- 2004-07-05 MX MXPA06000267A patent/MXPA06000267A/es unknown
- 2004-07-05 JP JP2006518113A patent/JP2009513514A/ja active Pending
- 2004-07-05 US US10/563,725 patent/US20060178513A1/en not_active Abandoned
- 2004-07-05 KR KR1020067000257A patent/KR20060032997A/ko not_active Application Discontinuation
- 2004-07-05 BR BRPI0412486-3A patent/BRPI0412486A/pt not_active IP Right Cessation
-
2005
- 2005-12-20 IL IL172698A patent/IL172698A0/en unknown
-
2006
- 2006-01-02 CR CR8162A patent/CR8162A/es not_active Application Discontinuation
- 2006-01-09 EC EC2006006275A patent/ECSP066275A/es unknown
- 2006-01-09 ZA ZA200600209A patent/ZA200600209B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CN1845673A (zh) | 2006-10-11 |
| CR8162A (es) | 2006-07-27 |
| JP2009513514A (ja) | 2009-04-02 |
| BRPI0412486A (pt) | 2006-09-19 |
| MXPA06000267A (es) | 2006-04-07 |
| US20060178513A1 (en) | 2006-08-10 |
| IL172698A0 (en) | 2006-04-10 |
| ECSP066275A (es) | 2006-07-28 |
| KR20060032997A (ko) | 2006-04-18 |
| EP1656020A2 (de) | 2006-05-17 |
| WO2005004606A3 (en) | 2005-04-21 |
| WO2005004606A2 (en) | 2005-01-20 |
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