JPWO2018069842A5

JPWO2018069842A5 -

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Publication number: JPWO2018069842A5
Authority: JP; Japan
Prior art keywords: ethyl; amino; phenyl; methylformimideamide; serial number
Prior art date: 2022-03-09
Legal status : Pending

Application number

JP2019541895A

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English (en)

Japanese (ja)

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JP2019532107A (ja

JP2019532107A5 (https=

Publication date

2022-03-09

2017-10-11 Application filed filed Critical

2017-10-11 Priority claimed from PCT/IB2017/056277 external-priority patent/WO2018069842A1/en

2019-11-07 Publication of JP2019532107A publication Critical patent/JP2019532107A/ja

2022-03-09 Publication of JP2019532107A5 publication Critical patent/JP2019532107A5/ja

2022-03-09 Publication of JPWO2018069842A5 publication Critical patent/JPWO2018069842A5/ja

Status Pending legal-status Critical Current

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-1 C1-6 -haloalkylthio Chemical group 0.000 claims description 248
241000196324 Embryophyta Species 0.000 claims description 230
150000001875 compounds Chemical class 0.000 claims description 207
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 121
239000000203 mixture Substances 0.000 claims description 106
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 69
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 62
229910052717 sulfur Inorganic materials 0.000 claims description 54
238000000034 method Methods 0.000 claims description 51
239000001257 hydrogen Substances 0.000 claims description 42
229910052739 hydrogen Inorganic materials 0.000 claims description 42
229910052760 oxygen Inorganic materials 0.000 claims description 39
150000001408 amides Chemical class 0.000 claims description 38
235000013399 edible fruits Nutrition 0.000 claims description 37
229910052757 nitrogen Inorganic materials 0.000 claims description 37
125000004429 atom Chemical group 0.000 claims description 35
125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 34
229910052799 carbon Inorganic materials 0.000 claims description 34
244000005700 microbiome Species 0.000 claims description 34
241000233866 Fungi Species 0.000 claims description 29
125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 26
230000003032 phytopathogenic effect Effects 0.000 claims description 26
239000000126 substance Substances 0.000 claims description 25
125000005842 heteroatom Chemical group 0.000 claims description 23
125000004122 cyclic group Chemical group 0.000 claims description 22
125000004641 (C1-C12) haloalkyl group Chemical group 0.000 claims description 20
125000004432 carbon atom Chemical group C* 0.000 claims description 19
125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 18
125000001424 substituent group Chemical group 0.000 claims description 18
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235000007164 Oryza sativa Nutrition 0.000 claims description 16
240000003768 Solanum lycopersicum Species 0.000 claims description 16
235000009566 rice Nutrition 0.000 claims description 16
125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 claims description 15
235000007688 Lycopersicon esculentum Nutrition 0.000 claims description 14
235000013339 cereals Nutrition 0.000 claims description 14
150000003839 salts Chemical class 0.000 claims description 14
HNQIVZYLYMDVSB-UHFFFAOYSA-N methanesulfonimidic acid Chemical compound CS(N)(=O)=O HNQIVZYLYMDVSB-UHFFFAOYSA-N 0.000 claims description 12
125000006625 (C3-C8) cycloalkyloxy group Chemical group 0.000 claims description 11
125000004643 (C1-C12) haloalkoxy group Chemical group 0.000 claims description 10
125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 10
241000238631 Hexapoda Species 0.000 claims description 10
241000244206 Nematoda Species 0.000 claims description 10
244000038559 crop plants Species 0.000 claims description 10
239000000417 fungicide Substances 0.000 claims description 10
239000004009 herbicide Substances 0.000 claims description 10
239000005871 repellent Substances 0.000 claims description 10
230000002940 repellent Effects 0.000 claims description 10
125000000623 heterocyclic group Chemical group 0.000 claims description 9
125000004207 3-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(OC([H])([H])[H])=C1[H] 0.000 claims description 8
241000894006 Bacteria Species 0.000 claims description 8
ZTQBHLJFTXXKAA-UHFFFAOYSA-N O=S(=O)NCC1=CC=CC=C1 Chemical compound O=S(=O)NCC1=CC=CC=C1 ZTQBHLJFTXXKAA-UHFFFAOYSA-N 0.000 claims description 8
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UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
GNNMYBXYNZJGKO-UHFFFAOYSA-N N-(3-chlorophenyl)-N,2,5-trimethyl-4-(morpholin-4-ylmethylideneamino)aniline Chemical compound ClC=1C=C(C=CC=1)N(C1=C(C=C(C(=C1)C)N=CN1CCOCC1)C)C GNNMYBXYNZJGKO-UHFFFAOYSA-N 0.000 claims description 6
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125000001786 isothiazolyl group Chemical group 0.000 claims description 6
125000001624 naphthyl group Chemical group 0.000 claims description 6
239000005645 nematicide Substances 0.000 claims description 6
125000001715 oxadiazolyl group Chemical group 0.000 claims description 6
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125000000335 thiazolyl group Chemical group 0.000 claims description 6
125000001544 thienyl group Chemical group 0.000 claims description 6
125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims description 5
XFWZWNDTUPRMTO-UHFFFAOYSA-N 5-chloro-N-(2-fluorophenyl)-N,2-dimethyl-4-(morpholin-4-ylmethylideneamino)aniline Chemical compound ClC=1C(=CC(=C(N(C)C2=C(C=CC=C2)F)C=1)C)N=CN1CCOCC1 XFWZWNDTUPRMTO-UHFFFAOYSA-N 0.000 claims description 5
244000291564 Allium cepa Species 0.000 claims description 5
235000002732 Allium cepa var. cepa Nutrition 0.000 claims description 5
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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 description 5
235000002595 Solanum tuberosum Nutrition 0.000 claims description 5
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125000003342 alkenyl group Chemical group 0.000 claims description 5
229910052736 halogen Inorganic materials 0.000 claims description 5
239000005648 plant growth regulator Substances 0.000 claims description 5
125000004076 pyridyl group Chemical group 0.000 claims description 5
125000006652 (C3-C12) cycloalkyl group Chemical group 0.000 claims description 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 description 4
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239000002184 metal Chemical class 0.000 claims description 4
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125000002971 oxazolyl group Chemical group 0.000 claims description 4
125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 claims description 3
AXOYPONQSPUQKG-UHFFFAOYSA-N 5-chloro-N-(2-fluorophenyl)-N,2-dimethyl-4-(thiomorpholin-4-ylmethylideneamino)aniline Chemical compound ClC=1C(=CC(=C(N(C)C2=C(C=CC=C2)F)C=1)C)N=CN1CCSCC1 AXOYPONQSPUQKG-UHFFFAOYSA-N 0.000 claims description 3
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 description 3
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 description 3
VQYCJTDLYFQHDJ-UHFFFAOYSA-N N-[5-chloro-4-[[ethyl(methyl)amino]methylideneamino]-2-methylphenyl]-N-phenylpropanamide Chemical compound CCN(C)C=NC1=CC(C)=C(C=C1Cl)N(C(=O)CC)C1=CC=CC=C1 VQYCJTDLYFQHDJ-UHFFFAOYSA-N 0.000 claims description 3
NNDHCURZZWRJGJ-UHFFFAOYSA-N O=S(=O)NCCC1=CC=CC=C1 Chemical compound O=S(=O)NCCC1=CC=CC=C1 NNDHCURZZWRJGJ-UHFFFAOYSA-N 0.000 claims description 3
244000299461 Theobroma cacao Species 0.000 claims description 3
235000005764 Theobroma cacao ssp. cacao Nutrition 0.000 claims description 3
235000005767 Theobroma cacao ssp. sphaerocarpum Nutrition 0.000 claims description 3
125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 claims description 3
125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 claims description 3
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239000003513 alkali Substances 0.000 claims description 2
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JP2019541895A 2016-10-14 2017-10-11 望ましくない植物病原性微生物と戦うことで作物を保護するための４−アミノ置換フェニルアミジン誘導体およびその使用 Pending JP2019532107A (ja)