RU2019114164A - Производные 4-замещенного фениламина и их использование для защиты культур от нежелательных фитопатогенных микроорганизмов - Google Patents
Производные 4-замещенного фениламина и их использование для защиты культур от нежелательных фитопатогенных микроорганизмов Download PDFInfo
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- RU2019114164A RU2019114164A RU2019114164A RU2019114164A RU2019114164A RU 2019114164 A RU2019114164 A RU 2019114164A RU 2019114164 A RU2019114164 A RU 2019114164A RU 2019114164 A RU2019114164 A RU 2019114164A RU 2019114164 A RU2019114164 A RU 2019114164A
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- ethyl
- amino
- methylformimidamide
- phenyl
- methyl
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- -1 4-SUBSTITUTED PHENYLAMINE Chemical class 0.000 title claims 32
- 230000003032 phytopathogenic effect Effects 0.000 title claims 8
- 244000005700 microbiome Species 0.000 title claims 5
- 150000001875 compounds Chemical class 0.000 claims 18
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 18
- 229910052717 sulfur Inorganic materials 0.000 claims 18
- 125000004429 atom Chemical group 0.000 claims 14
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 13
- 239000000203 mixture Substances 0.000 claims 13
- 229910052760 oxygen Inorganic materials 0.000 claims 13
- 229910052739 hydrogen Inorganic materials 0.000 claims 12
- 239000001257 hydrogen Substances 0.000 claims 12
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 12
- 125000000217 alkyl group Chemical group 0.000 claims 11
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 10
- 229910052799 carbon Inorganic materials 0.000 claims 10
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 10
- 229910052757 nitrogen Inorganic materials 0.000 claims 10
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 7
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 7
- 125000004641 (C1-C12) haloalkyl group Chemical group 0.000 claims 6
- 241000196324 Embryophyta Species 0.000 claims 6
- 125000004432 carbon atom Chemical group C* 0.000 claims 6
- 125000005842 heteroatom Chemical group 0.000 claims 6
- 230000002265 prevention Effects 0.000 claims 5
- 125000004643 (C1-C12) haloalkoxy group Chemical group 0.000 claims 4
- 125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 claims 4
- QBASDPMKHNDCKF-UHFFFAOYSA-N N'-[2,5-dimethyl-4-[2-(trifluoromethoxy)anilino]phenyl]-N-ethyl-N-methylmethanimidamide Chemical compound CC1=C(C=C(C(=C1)NC1=C(C=CC=C1)OC(F)(F)F)C)N=CN(C)CC QBASDPMKHNDCKF-UHFFFAOYSA-N 0.000 claims 4
- 125000003545 alkoxy group Chemical group 0.000 claims 4
- 125000004122 cyclic group Chemical group 0.000 claims 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 4
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 claims 3
- 241000233866 Fungi Species 0.000 claims 3
- 150000001204 N-oxides Chemical class 0.000 claims 3
- 125000003342 alkenyl group Chemical group 0.000 claims 3
- 125000003118 aryl group Chemical group 0.000 claims 3
- 150000003839 salts Chemical class 0.000 claims 3
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims 2
- 125000006625 (C3-C8) cycloalkyloxy group Chemical group 0.000 claims 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims 2
- 241000894006 Bacteria Species 0.000 claims 2
- 241000207199 Citrus Species 0.000 claims 2
- PNKUSGQVOMIXLU-UHFFFAOYSA-N Formamidine Chemical compound NC=N PNKUSGQVOMIXLU-UHFFFAOYSA-N 0.000 claims 2
- 241000238631 Hexapoda Species 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- 241000699670 Mus sp. Species 0.000 claims 2
- 241000244206 Nematoda Species 0.000 claims 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims 2
- 235000020971 citrus fruits Nutrition 0.000 claims 2
- 235000013399 edible fruits Nutrition 0.000 claims 2
- 229910052736 halogen Inorganic materials 0.000 claims 2
- 125000000623 heterocyclic group Chemical group 0.000 claims 2
- 208000015181 infectious disease Diseases 0.000 claims 2
- 125000001786 isothiazolyl group Chemical group 0.000 claims 2
- 125000000842 isoxazolyl group Chemical group 0.000 claims 2
- 125000001624 naphthyl group Chemical group 0.000 claims 2
- 125000001715 oxadiazolyl group Chemical group 0.000 claims 2
- 125000002971 oxazolyl group Chemical group 0.000 claims 2
- 125000002098 pyridazinyl group Chemical group 0.000 claims 2
- 125000004076 pyridyl group Chemical group 0.000 claims 2
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 2
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 claims 2
- 125000001424 substituent group Chemical group 0.000 claims 2
- 125000001113 thiadiazolyl group Chemical group 0.000 claims 2
- 125000000335 thiazolyl group Chemical group 0.000 claims 2
- 244000045561 useful plants Species 0.000 claims 2
- 125000006652 (C3-C12) cycloalkyl group Chemical group 0.000 claims 1
- XTFIVUDBNACUBN-UHFFFAOYSA-N 1,3,5-trinitro-1,3,5-triazinane Chemical compound [O-][N+](=O)N1CN([N+]([O-])=O)CN([N+]([O-])=O)C1 XTFIVUDBNACUBN-UHFFFAOYSA-N 0.000 claims 1
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 claims 1
- 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 claims 1
- 235000006667 Aleurites moluccana Nutrition 0.000 claims 1
- 244000291564 Allium cepa Species 0.000 claims 1
- 235000002732 Allium cepa var. cepa Nutrition 0.000 claims 1
- 235000000832 Ayote Nutrition 0.000 claims 1
- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 claims 1
- 235000002566 Capsicum Nutrition 0.000 claims 1
- 240000007154 Coffea arabica Species 0.000 claims 1
- 229920000742 Cotton Polymers 0.000 claims 1
- 240000004244 Cucurbita moschata Species 0.000 claims 1
- 235000009854 Cucurbita moschata Nutrition 0.000 claims 1
- 235000009804 Cucurbita pepo subsp pepo Nutrition 0.000 claims 1
- 235000010469 Glycine max Nutrition 0.000 claims 1
- 241000219146 Gossypium Species 0.000 claims 1
- 240000007049 Juglans regia Species 0.000 claims 1
- 235000009496 Juglans regia Nutrition 0.000 claims 1
- 235000007688 Lycopersicon esculentum Nutrition 0.000 claims 1
- CMMPJERXJCVMLT-UHFFFAOYSA-N N'-(4-anilino-2,5-dimethylphenyl)-N-ethyl-N-methylmethanimidamide Chemical compound CC1=C(C=C(C(=C1)NC1=CC=CC=C1)C)N=CN(C)CC CMMPJERXJCVMLT-UHFFFAOYSA-N 0.000 claims 1
- FYLXCPQSCWMBTD-UHFFFAOYSA-N N'-(4-anilino-2-bromo-6-fluoro-3-methylphenyl)-N-ethyl-N-methylmethanimidamide Chemical compound BrC1=C(C(=CC(=C1C)NC1=CC=CC=C1)F)N=CN(C)CC FYLXCPQSCWMBTD-UHFFFAOYSA-N 0.000 claims 1
- IYFAFDYJGGVFLR-UHFFFAOYSA-N N'-(4-anilino-2-chloro-5-methylphenyl)-N-ethyl-N-methylmethanimidamide Chemical compound ClC1=C(C=C(C(=C1)NC1=CC=CC=C1)C)N=CN(C)CC IYFAFDYJGGVFLR-UHFFFAOYSA-N 0.000 claims 1
- BFXLDPRJMNARGZ-UHFFFAOYSA-N N'-(4-anilino-5-fluoro-2-methylphenyl)-N-ethyl-N-methylmethanimidamide Chemical compound C(C)N(C=NC1=C(C=C(C(=C1)F)NC1=CC=CC=C1)C)C BFXLDPRJMNARGZ-UHFFFAOYSA-N 0.000 claims 1
- XJWPBTNDXWEPFP-UHFFFAOYSA-N N'-[2,5-dimethyl-4-(2-methylanilino)phenyl]-N-ethyl-N-methylmethanimidamide Chemical compound CC1=C(C=C(C(=C1)NC1=C(C=CC=C1)C)C)N=CN(C)CC XJWPBTNDXWEPFP-UHFFFAOYSA-N 0.000 claims 1
- KMIYDNUIHCAFKR-UHFFFAOYSA-N N'-[2,5-dimethyl-4-(2-methylsulfanylanilino)phenyl]-N-ethyl-N-methylmethanimidamide Chemical compound CC1=C(C=C(C(=C1)NC1=C(C=CC=C1)SC)C)N=CN(C)CC KMIYDNUIHCAFKR-UHFFFAOYSA-N 0.000 claims 1
- UMNIOSZVRDWLCW-UHFFFAOYSA-N N'-[2,5-dimethyl-4-(3-methylsulfanylanilino)phenyl]-N-ethyl-N-methylmethanimidamide Chemical compound CC1=C(C=C(C(=C1)NC1=CC(=CC=C1)SC)C)N=CN(C)CC UMNIOSZVRDWLCW-UHFFFAOYSA-N 0.000 claims 1
- CLXSPRFLQXUWED-UHFFFAOYSA-N N'-[2,5-dimethyl-4-(4-methylanilino)phenyl]-N-ethyl-N-methylmethanimidamide Chemical compound CC1=C(C=C(C(=C1)NC1=CC=C(C=C1)C)C)N=CN(C)CC CLXSPRFLQXUWED-UHFFFAOYSA-N 0.000 claims 1
- WEIUIJLEXFDCBX-UHFFFAOYSA-N N'-[2,5-dimethyl-4-(4-methylsulfanylanilino)phenyl]-N-ethyl-N-methylmethanimidamide Chemical compound CC1=C(C=C(C(=C1)NC1=CC=C(C=C1)SC)C)N=CN(C)CC WEIUIJLEXFDCBX-UHFFFAOYSA-N 0.000 claims 1
- DMHKCENOJQTZMI-UHFFFAOYSA-N N'-[2,5-dimethyl-4-(N-methyl-3-methylsulfanylanilino)phenyl]-N-ethyl-N-methylmethanimidamide Chemical compound CC1=C(C=C(C(=C1)N(C1=CC(=CC=C1)SC)C)C)N=CN(C)CC DMHKCENOJQTZMI-UHFFFAOYSA-N 0.000 claims 1
- CDDMPXOUVYQICG-UHFFFAOYSA-N N'-[2,5-dimethyl-4-(N-methyl-4-methylsulfanylanilino)phenyl]-N-ethyl-N-methylmethanimidamide Chemical compound CC1=C(C=C(C(=C1)N(C1=CC=C(C=C1)SC)C)C)N=CN(C)CC CDDMPXOUVYQICG-UHFFFAOYSA-N 0.000 claims 1
- FHOOAISBRLMWEN-UHFFFAOYSA-N N'-[2,5-dimethyl-4-(N-methylanilino)phenyl]-N-ethyl-N-methylmethanimidamide Chemical compound CC1=C(C=C(C(=C1)N(C1=CC=CC=C1)C)C)N=CN(C)CC FHOOAISBRLMWEN-UHFFFAOYSA-N 0.000 claims 1
- IRDHFMOFCJRMIQ-UHFFFAOYSA-N N'-[2,5-dimethyl-4-(N-methylsulfonylanilino)phenyl]-N-ethyl-N-methylmethanimidamide Chemical compound CC1=C(C=C(C(=C1)N(S(=O)(=O)C)C1=CC=CC=C1)C)N=CN(C)CC IRDHFMOFCJRMIQ-UHFFFAOYSA-N 0.000 claims 1
- RZCIPHUKWCWEIB-UHFFFAOYSA-N N'-[2,5-dimethyl-4-(pyridin-2-ylamino)phenyl]-N-ethyl-N-methylmethanimidamide Chemical compound CC1=C(C=C(C(=C1)NC1=NC=CC=C1)C)N=CN(C)CC RZCIPHUKWCWEIB-UHFFFAOYSA-N 0.000 claims 1
- FXQXTHICPBZFHD-UHFFFAOYSA-N N'-[2,5-dimethyl-4-[(5-oxo-7,8-dihydro-6H-naphthalen-2-yl)amino]phenyl]-N-ethyl-N-methylmethanimidamide Chemical compound CC1=C(C=C(C(=C1)NC1=CC=2CCCC(C=2C=C1)=O)C)N=CN(C)CC FXQXTHICPBZFHD-UHFFFAOYSA-N 0.000 claims 1
- CFZPJBAEQLHIIN-UHFFFAOYSA-N N'-[2,5-dimethyl-4-[2-(trifluoromethyl)anilino]phenyl]-N-ethyl-N-methylmethanimidamide Chemical compound CC1=C(C=C(C(=C1)NC1=C(C=CC=C1)C(F)(F)F)C)N=CN(C)CC CFZPJBAEQLHIIN-UHFFFAOYSA-N 0.000 claims 1
- FNPIUUDVTPOLOT-UHFFFAOYSA-N N'-[2,5-dimethyl-4-[2-(trifluoromethylsulfanyl)anilino]phenyl]-N-ethyl-N-methylmethanimidamide Chemical compound CC1=C(C=C(C(=C1)NC1=C(C=CC=C1)SC(F)(F)F)C)N=CN(C)CC FNPIUUDVTPOLOT-UHFFFAOYSA-N 0.000 claims 1
- ABCUGJUCLXLSHV-UHFFFAOYSA-N N'-[2,5-dimethyl-4-[3-(1,1,2,2-tetrafluoroethoxy)anilino]phenyl]-N-ethyl-N-methylmethanimidamide Chemical compound CC1=C(C=C(C(=C1)NC1=CC(=CC=C1)OC(C(F)F)(F)F)C)N=CN(C)CC ABCUGJUCLXLSHV-UHFFFAOYSA-N 0.000 claims 1
- KYUVYPIPEOYWGT-UHFFFAOYSA-N N'-[2,5-dimethyl-4-[3-(trifluoromethoxy)anilino]phenyl]-N-ethyl-N-methylmethanimidamide Chemical compound CC1=C(C=C(C(=C1)NC1=CC(=CC=C1)OC(F)(F)F)C)N=CN(C)CC KYUVYPIPEOYWGT-UHFFFAOYSA-N 0.000 claims 1
- FHTUAPULXZXHHQ-UHFFFAOYSA-N N'-[2,5-dimethyl-4-[3-(trifluoromethyl)anilino]phenyl]-N-ethyl-N-methylmethanimidamide Chemical compound CC1=C(C=C(C(=C1)NC1=CC(=CC=C1)C(F)(F)F)C)N=CN(C)CC FHTUAPULXZXHHQ-UHFFFAOYSA-N 0.000 claims 1
- CNIKCCQQSQTHIG-UHFFFAOYSA-N N'-[2,5-dimethyl-4-[3-(trifluoromethylsulfanyl)anilino]phenyl]-N-ethyl-N-methylmethanimidamide Chemical compound CC1=C(C=C(C(=C1)NC1=CC(=CC=C1)SC(F)(F)F)C)N=CN(C)CC CNIKCCQQSQTHIG-UHFFFAOYSA-N 0.000 claims 1
- VUZCGETUINSYOJ-UHFFFAOYSA-N N'-[2,5-dimethyl-4-[4-(trifluoromethoxy)anilino]phenyl]-N-ethyl-N-methylmethanimidamide Chemical compound CC1=C(C=C(C(=C1)NC1=CC=C(C=C1)OC(F)(F)F)C)N=CN(C)CC VUZCGETUINSYOJ-UHFFFAOYSA-N 0.000 claims 1
- GWMVLLGGKICRBD-UHFFFAOYSA-N N'-[2,5-dimethyl-4-[4-(trifluoromethylsulfanyl)anilino]phenyl]-N-ethyl-N-methylmethanimidamide Chemical compound CC1=C(C=C(C(=C1)NC1=CC=C(C=C1)SC(F)(F)F)C)N=CN(C)CC GWMVLLGGKICRBD-UHFFFAOYSA-N 0.000 claims 1
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- GCISFBSHNNZNJB-UHFFFAOYSA-N N'-[2,5-dimethyl-4-[N-methyl-2-(trifluoromethyl)anilino]phenyl]-N-ethyl-N-methylmethanimidamide Chemical compound CC1=C(C=C(C(=C1)N(C1=C(C=CC=C1)C(F)(F)F)C)C)N=CN(C)CC GCISFBSHNNZNJB-UHFFFAOYSA-N 0.000 claims 1
- IKCKDEKSDROHQL-UHFFFAOYSA-N N'-[2,5-dimethyl-4-[N-methyl-2-(trifluoromethylsulfanyl)anilino]phenyl]-N-ethyl-N-methylmethanimidamide Chemical compound CC1=C(C=C(C(=C1)N(C1=C(C=CC=C1)SC(F)(F)F)C)C)N=CN(C)CC IKCKDEKSDROHQL-UHFFFAOYSA-N 0.000 claims 1
- QMRQJSPBIHUHBU-UHFFFAOYSA-N N'-[2,5-dimethyl-4-[N-methyl-3,5-bis(trifluoromethyl)anilino]phenyl]-N-ethyl-N-methylmethanimidamide Chemical compound FC(C=1C=C(C=C(C=1)C(F)(F)F)N(C1=CC(=C(C=C1C)N=CN(C)CC)C)C)(F)F QMRQJSPBIHUHBU-UHFFFAOYSA-N 0.000 claims 1
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- NKHGKSMLYSGETN-UHFFFAOYSA-N N'-[7-(4-chloroanilino)-2,3-dihydro-1H-inden-4-yl]-N-ethyl-N-methylmethanimidamide Chemical compound ClC1=CC=C(C=C1)NC=1C=CC(=C2CCCC=12)N=CN(C)CC NKHGKSMLYSGETN-UHFFFAOYSA-N 0.000 claims 1
- ARMAWOZYLJULEI-UHFFFAOYSA-N N-(3-chlorophenyl)-N,2,5-trimethyl-4-(piperidin-1-ylmethylideneamino)aniline Chemical compound ClC=1C=C(C=CC=1)N(C1=C(C=C(C(=C1)C)N=CN1CCCCC1)C)C ARMAWOZYLJULEI-UHFFFAOYSA-N 0.000 claims 1
- WJTBKCCSIUYAST-UHFFFAOYSA-N N-[4-[[ethyl(methyl)amino]methylideneamino]-2,5-dimethylphenyl]-N-phenylacetamide Chemical compound CCN(C)C=NC1=CC(C)=C(C=C1C)N(C(C)=O)C1=CC=CC=C1 WJTBKCCSIUYAST-UHFFFAOYSA-N 0.000 claims 1
- XTGXKSYFWJAIFF-UHFFFAOYSA-N N-[5-chloro-4-[[ethyl(methyl)amino]methylideneamino]-2-methylphenyl]-N-phenylacetamide Chemical compound ClC=1C(=CC(=C(C=1)N(C(C)=O)C1=CC=CC=C1)C)N=CN(C)CC XTGXKSYFWJAIFF-UHFFFAOYSA-N 0.000 claims 1
- IGALFMGMIRSNRE-UHFFFAOYSA-N N-ethyl-N'-[4-(2-fluoro-5-methylanilino)-2,5-dimethylphenyl]-N-methylmethanimidamide Chemical compound C(C)N(C=NC1=C(C=C(C(=C1)C)NC1=C(C=CC(=C1)C)F)C)C IGALFMGMIRSNRE-UHFFFAOYSA-N 0.000 claims 1
- GVETXSMJRUUCED-UHFFFAOYSA-N N-ethyl-N'-[4-(2-fluoro-N,5-dimethylanilino)-2,5-dimethylphenyl]-N-methylmethanimidamide Chemical compound C(C)N(C=NC1=C(C=C(C(=C1)C)N(C)C1=C(C=CC(=C1)C)F)C)C GVETXSMJRUUCED-UHFFFAOYSA-N 0.000 claims 1
- UJJLNBBEZRPBIX-UHFFFAOYSA-N N-ethyl-N'-[4-(2-fluoro-N-methylanilino)-2,5-dimethylphenyl]-N-methylmethanimidamide Chemical compound C(C)N(C=NC1=C(C=C(C(=C1)C)N(C)C1=C(C=CC=C1)F)C)C UJJLNBBEZRPBIX-UHFFFAOYSA-N 0.000 claims 1
- ZNOZGTMPAAOJLG-UHFFFAOYSA-N N-ethyl-N'-[4-(2-methoxy-N-methylanilino)-2,5-dimethylphenyl]-N-methylmethanimidamide Chemical compound C(C)N(C=NC1=C(C=C(C(=C1)C)N(C)C1=C(C=CC=C1)OC)C)C ZNOZGTMPAAOJLG-UHFFFAOYSA-N 0.000 claims 1
- ZGFXNWIZJHGOHV-UHFFFAOYSA-N N-ethyl-N'-[4-(3-fluoro-N-methylanilino)-2,5-dimethylphenyl]-N-methylmethanimidamide Chemical compound C(C)N(C=NC1=C(C=C(C(=C1)C)N(C)C1=CC(=CC=C1)F)C)C ZGFXNWIZJHGOHV-UHFFFAOYSA-N 0.000 claims 1
- NFEPBKJANDCECS-UHFFFAOYSA-N N-ethyl-N'-[4-(3-fluoroanilino)-2,5-dimethylphenyl]-N-methylmethanimidamide Chemical compound C(C)N(C=NC1=C(C=C(C(=C1)C)NC1=CC(=CC=C1)F)C)C NFEPBKJANDCECS-UHFFFAOYSA-N 0.000 claims 1
- MCYXPLUFAJRSEI-UHFFFAOYSA-N N-ethyl-N'-[4-(3-methoxy-N-methylanilino)-2,5-dimethylphenyl]-N-methylmethanimidamide Chemical compound C(C)N(C=NC1=C(C=C(C(=C1)C)N(C)C1=CC(=CC=C1)OC)C)C MCYXPLUFAJRSEI-UHFFFAOYSA-N 0.000 claims 1
- RLCDSNCIIATDHT-UHFFFAOYSA-N N-ethyl-N'-[4-(4-fluoro-3-methoxy-N-methylanilino)-2,5-dimethylphenyl]-N-methylmethanimidamide Chemical compound C(C)N(C=NC1=C(C=C(C(=C1)C)N(C)C1=CC(=C(C=C1)F)OC)C)C RLCDSNCIIATDHT-UHFFFAOYSA-N 0.000 claims 1
- KBMZTKGQPSGXRO-UHFFFAOYSA-N N-ethyl-N'-[4-(4-fluoro-3-methoxyanilino)-2,5-dimethylphenyl]-N-methylmethanimidamide Chemical compound C(C)N(C=NC1=C(C=C(C(=C1)C)NC1=CC(=C(C=C1)F)OC)C)C KBMZTKGQPSGXRO-UHFFFAOYSA-N 0.000 claims 1
- SPNJTFHZQSYGDX-UHFFFAOYSA-N N-ethyl-N'-[4-(4-fluoro-N-methylanilino)-2,5-dimethylphenyl]-N-methylmethanimidamide Chemical compound C(C)N(C=NC1=C(C=C(C(=C1)C)N(C)C1=CC=C(C=C1)F)C)C SPNJTFHZQSYGDX-UHFFFAOYSA-N 0.000 claims 1
- RVMAPKWMMPDYQF-UHFFFAOYSA-N N-ethyl-N'-[4-(4-methoxy-N-methylanilino)-2,5-dimethylphenyl]-N-methylmethanimidamide Chemical compound C(C)N(C=NC1=C(C=C(C(=C1)C)N(C)C1=CC=C(C=C1)OC)C)C RVMAPKWMMPDYQF-UHFFFAOYSA-N 0.000 claims 1
- RFLWRMPFLQZAEW-UHFFFAOYSA-N N-ethyl-N'-[4-[4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-N,2-dimethylanilino]-2,5-dimethylphenyl]-N-methylmethanimidamide Chemical compound CC1=C(C=C(C(=C1)N(C1=C(C=C(C=C1)C(C(F)(F)F)(C(F)(F)F)F)C)C)C)N=CN(C)CC RFLWRMPFLQZAEW-UHFFFAOYSA-N 0.000 claims 1
- PMIFFKMFGPNSAV-UHFFFAOYSA-N N-ethyl-N'-[4-[4-fluoro-3-(1,1,2,2-tetrafluoroethoxy)anilino]-2,5-dimethylphenyl]-N-methylmethanimidamide Chemical compound C(C)N(C=NC1=C(C=C(C(=C1)C)NC1=CC(=C(C=C1)F)OC(C(F)F)(F)F)C)C PMIFFKMFGPNSAV-UHFFFAOYSA-N 0.000 claims 1
- MRUIHVFZTOYPFG-UHFFFAOYSA-N N-ethyl-N'-[5-fluoro-2-methyl-4-(N-methylanilino)phenyl]-N-methylmethanimidamide Chemical compound C(C)N(C=NC1=C(C=C(C(=C1)F)N(C1=CC=CC=C1)C)C)C MRUIHVFZTOYPFG-UHFFFAOYSA-N 0.000 claims 1
- LSRURVNDORUDBI-UHFFFAOYSA-N N-ethyl-N'-[5-fluoro-4-(2-fluoroanilino)-2-methylphenyl]-N-methylmethanimidamide Chemical compound C(C)N(C=NC1=C(C=C(C(=C1)F)NC1=C(C=CC=C1)F)C)C LSRURVNDORUDBI-UHFFFAOYSA-N 0.000 claims 1
- VAHHBSANZIIPEZ-UHFFFAOYSA-N N-ethyl-N'-[5-fluoro-4-(4-methoxy-N-methylanilino)-2-methylphenyl]-N-methylmethanimidamide Chemical compound C(C)N(C=NC1=C(C=C(C(=C1)F)N(C)C1=CC=C(C=C1)OC)C)C VAHHBSANZIIPEZ-UHFFFAOYSA-N 0.000 claims 1
- KLZUGDFKZCPNQJ-UHFFFAOYSA-N N-ethyl-N'-[5-fluoro-4-(4-methoxyanilino)-2-methylphenyl]-N-methylmethanimidamide Chemical compound C(C)N(C=NC1=C(C=C(C(=C1)F)NC1=CC=C(C=C1)OC)C)C KLZUGDFKZCPNQJ-UHFFFAOYSA-N 0.000 claims 1
- AZLQLIPASKOOTB-UHFFFAOYSA-N N-ethyl-N'-[5-fluoro-4-[4-fluoro-N-methyl-3-(1,1,2,2-tetrafluoroethoxy)anilino]-2-methylphenyl]-N-methylmethanimidamide Chemical compound C(C)N(C=NC1=C(C=C(C(=C1)F)N(C)C1=CC(=C(C=C1)F)OC(C(F)F)(F)F)C)C AZLQLIPASKOOTB-UHFFFAOYSA-N 0.000 claims 1
- JZMRYHHMLRVDLB-UHFFFAOYSA-N N-ethyl-N'-[7-(2-methoxyanilino)-2,3-dihydro-1H-inden-4-yl]-N-methylmethanimidamide Chemical compound C(C)N(C=NC1=C2CCCC2=C(C=C1)NC1=C(C=CC=C1)OC)C JZMRYHHMLRVDLB-UHFFFAOYSA-N 0.000 claims 1
- 244000061176 Nicotiana tabacum Species 0.000 claims 1
- 235000002637 Nicotiana tabacum Nutrition 0.000 claims 1
- 240000007594 Oryza sativa Species 0.000 claims 1
- 235000007164 Oryza sativa Nutrition 0.000 claims 1
- 241000758706 Piperaceae Species 0.000 claims 1
- 240000000111 Saccharum officinarum Species 0.000 claims 1
- 235000007201 Saccharum officinarum Nutrition 0.000 claims 1
- 240000003768 Solanum lycopersicum Species 0.000 claims 1
- 244000061456 Solanum tuberosum Species 0.000 claims 1
- 235000002595 Solanum tuberosum Nutrition 0.000 claims 1
- 235000021536 Sugar beet Nutrition 0.000 claims 1
- 244000269722 Thea sinensis Species 0.000 claims 1
- 235000009470 Theobroma cacao Nutrition 0.000 claims 1
- 244000299461 Theobroma cacao Species 0.000 claims 1
- 235000021307 Triticum Nutrition 0.000 claims 1
- 244000098338 Triticum aestivum Species 0.000 claims 1
- 230000000895 acaricidal effect Effects 0.000 claims 1
- 239000000642 acaricide Substances 0.000 claims 1
- 125000002877 alkyl aryl group Chemical group 0.000 claims 1
- 125000004414 alkyl thio group Chemical group 0.000 claims 1
- 125000000304 alkynyl group Chemical group 0.000 claims 1
- 239000003242 anti bacterial agent Substances 0.000 claims 1
- 229940088710 antibiotic agent Drugs 0.000 claims 1
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 claims 1
- 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 claims 1
- 125000002619 bicyclic group Chemical group 0.000 claims 1
- 230000000853 biopesticidal effect Effects 0.000 claims 1
- 235000013339 cereals Nutrition 0.000 claims 1
- 235000016213 coffee Nutrition 0.000 claims 1
- 235000013353 coffee beverage Nutrition 0.000 claims 1
- 230000000052 comparative effect Effects 0.000 claims 1
- 125000005366 cycloalkylthio group Chemical group 0.000 claims 1
- 239000003337 fertilizer Substances 0.000 claims 1
- 239000000417 fungicide Substances 0.000 claims 1
- 125000002541 furyl group Chemical group 0.000 claims 1
- 125000000262 haloalkenyl group Chemical group 0.000 claims 1
- 125000004995 haloalkylthio group Chemical group 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 239000004009 herbicide Substances 0.000 claims 1
- 125000001072 heteroaryl group Chemical group 0.000 claims 1
- 125000004415 heterocyclylalkyl group Chemical group 0.000 claims 1
- 125000002883 imidazolyl group Chemical group 0.000 claims 1
- 239000002917 insecticide Substances 0.000 claims 1
- 125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 0.000 claims 1
- 235000021374 legumes Nutrition 0.000 claims 1
- 239000002184 metal Chemical class 0.000 claims 1
- 239000005645 nematicide Substances 0.000 claims 1
- 235000014571 nuts Nutrition 0.000 claims 1
- 239000005648 plant growth regulator Substances 0.000 claims 1
- 235000012015 potatoes Nutrition 0.000 claims 1
- 235000015136 pumpkin Nutrition 0.000 claims 1
- 125000003373 pyrazinyl group Chemical group 0.000 claims 1
- 125000003226 pyrazolyl group Chemical group 0.000 claims 1
- 125000000168 pyrrolyl group Chemical group 0.000 claims 1
- 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 claims 1
- 235000009566 rice Nutrition 0.000 claims 1
- 235000013616 tea Nutrition 0.000 claims 1
- 125000001544 thienyl group Chemical group 0.000 claims 1
- 125000001425 triazolyl group Chemical group 0.000 claims 1
- 239000013598 vector Substances 0.000 claims 1
- 235000013311 vegetables Nutrition 0.000 claims 1
Classifications
-
- 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
- A01N43/84—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 six-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,4
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C257/00—Compounds containing carboxyl groups, the doubly-bound oxygen atom of a carboxyl group being replaced by a doubly-bound nitrogen atom, this nitrogen atom not being further bound to an oxygen atom, e.g. imino-ethers, amidines
- C07C257/10—Compounds containing carboxyl groups, the doubly-bound oxygen atom of a carboxyl group being replaced by a doubly-bound nitrogen atom, this nitrogen atom not being further bound to an oxygen atom, e.g. imino-ethers, amidines with replacement of the other oxygen atom of the carboxyl group by nitrogen atoms, e.g. amidines
- C07C257/12—Compounds containing carboxyl groups, the doubly-bound oxygen atom of a carboxyl group being replaced by a doubly-bound nitrogen atom, this nitrogen atom not being further bound to an oxygen atom, e.g. imino-ethers, amidines with replacement of the other oxygen atom of the carboxyl group by nitrogen atoms, e.g. amidines having carbon atoms of amidino groups bound to hydrogen atoms
-
- 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
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/26—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds containing nitrogen-to-nitrogen bonds, e.g. azides, diazo-amino compounds, diazonium compounds, hydrazine derivatives
-
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/52—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing groups, e.g. carboxylic acid amidines
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C211/00—Compounds containing amino groups bound to a carbon skeleton
- C07C211/43—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
- C07C211/44—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having amino groups bound to only one six-membered aromatic ring
- C07C211/52—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having amino groups bound to only one six-membered aromatic ring the carbon skeleton being further substituted by halogen atoms or by nitro or nitroso groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C317/00—Sulfones; Sulfoxides
- C07C317/26—Sulfones; Sulfoxides having sulfone or sulfoxide groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton
- C07C317/32—Sulfones; Sulfoxides having sulfone or sulfoxide groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton with sulfone or sulfoxide groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/23—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton
- C07C323/39—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton at least one of the nitrogen atoms being part of any of the groups, X being a hetero atom, Y being any atom
- C07C323/40—Y being a hydrogen or a carbon atom
- C07C323/41—Y being a hydrogen or an acyclic carbon atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/23—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton
- C07C323/46—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton having at least one of the nitrogen atoms, not being part of nitro or nitroso groups, further bound to other hetero atoms
- C07C323/48—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton having at least one of the nitrogen atoms, not being part of nitro or nitroso groups, further bound to other hetero atoms to nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/08—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
- C07D211/10—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with radicals containing only carbon and hydrogen atoms attached to ring carbon atoms
- C07D211/12—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with radicals containing only carbon and hydrogen atoms attached to ring carbon atoms with only hydrogen atoms attached to the ring nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D265/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D265/28—1,4-Oxazines; Hydrogenated 1,4-oxazines
- C07D265/30—1,4-Oxazines; Hydrogenated 1,4-oxazines not condensed with other rings
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pyridine Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IN201611035246 | 2016-10-14 | ||
| IN201611035246 | 2016-10-14 | ||
| PCT/IB2017/056277 WO2018069842A1 (en) | 2016-10-14 | 2017-10-11 | 4-amino substituted phenylamidine derivatives and their use to protect crops by fighting undesired phytopathogenic micoorganisms |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| RU2019114164A true RU2019114164A (ru) | 2020-11-16 |
| RU2019114164A3 RU2019114164A3 (https=) | 2021-02-03 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2019114164A RU2019114164A (ru) | 2016-10-14 | 2017-10-11 | Производные 4-замещенного фениламина и их использование для защиты культур от нежелательных фитопатогенных микроорганизмов |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US20190367445A1 (https=) |
| EP (1) | EP3525589B1 (https=) |
| JP (1) | JP2019532107A (https=) |
| CN (1) | CN109890206A (https=) |
| AR (1) | AR109949A1 (https=) |
| AU (1) | AU2017342206B2 (https=) |
| BR (1) | BR112019007483B1 (https=) |
| CA (1) | CA3040408A1 (https=) |
| ES (1) | ES2972589T3 (https=) |
| MX (1) | MX2019004293A (https=) |
| RU (1) | RU2019114164A (https=) |
| TW (1) | TWI770071B (https=) |
| UY (1) | UY37443A (https=) |
| WO (1) | WO2018069842A1 (https=) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2020517608A (ja) * | 2017-04-20 | 2020-06-18 | ピーアイ インダストリーズ リミテッドPi Industries Ltd | 新規フェニルアミン化合物 |
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- 2017-10-11 EP EP17797733.7A patent/EP3525589B1/en active Active
- 2017-10-11 US US16/341,463 patent/US20190367445A1/en not_active Abandoned
- 2017-10-11 CA CA3040408A patent/CA3040408A1/en not_active Abandoned
- 2017-10-11 MX MX2019004293A patent/MX2019004293A/es unknown
- 2017-10-11 JP JP2019541895A patent/JP2019532107A/ja active Pending
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| AU2017342206B2 (en) | 2022-06-02 |
| TW201829374A (zh) | 2018-08-16 |
| JP2019532107A (ja) | 2019-11-07 |
| RU2019114164A3 (https=) | 2021-02-03 |
| MX2019004293A (es) | 2019-10-14 |
| CA3040408A1 (en) | 2018-04-19 |
| UY37443A (es) | 2018-05-31 |
| US20190367445A1 (en) | 2019-12-05 |
| BR112019007483A2 (pt) | 2019-10-08 |
| AU2017342206A1 (en) | 2019-04-04 |
| AR109949A1 (es) | 2019-02-06 |
| CN109890206A (zh) | 2019-06-14 |
| ES2972589T3 (es) | 2024-06-13 |
| WO2018069842A1 (en) | 2018-04-19 |
| EP3525589B1 (en) | 2023-12-06 |
| BR112019007483B1 (pt) | 2023-10-17 |
| TWI770071B (zh) | 2022-07-11 |
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