TW201441215A

TW201441215A - 新穎殺微生物劑

新穎殺微生物劑 Download PDF

Info

Publication number: TW201441215A
Authority: TW; Taiwan
Prior art keywords: group; alkyl; haloalkoxy; haloalkyl; compound
Prior art date: 2013-02-04

Application number

TW103103124A

Other languages

English (en)

Chinese (zh)

Inventor

Stephane Andre Marie Jeanmart

Damien Bonvalot

Original Assignee

Syngenta Participations Ag

Priority date

2013-02-04

Filing date

2014-01-28

Publication date

2014-11-01

2014-01-28 Application filed by Syngenta Participations Ag filed Critical Syngenta Participations Ag

2014-11-01 Publication of TW201441215A publication Critical patent/TW201441215A/zh

Links

230000003641 microbiacidal effect Effects 0.000 title 1
229940124561 microbicide Drugs 0.000 title 1
150000001875 compounds Chemical class 0.000 claims abstract description 227
239000000203 mixture Substances 0.000 claims abstract description 61
238000000034 method Methods 0.000 claims abstract description 36
-1 C 1 -C 4 alkoxy Chemical group 0.000 claims description 132
229910052736 halogen Inorganic materials 0.000 claims description 95
125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 88
150000002367 halogens Chemical class 0.000 claims description 86
125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims description 81
125000004093 cyano group Chemical group *C#N 0.000 claims description 79
125000003118 aryl group Chemical group 0.000 claims description 58
125000001424 substituent group Chemical group 0.000 claims description 50
239000001257 hydrogen Substances 0.000 claims description 43
229910052739 hydrogen Inorganic materials 0.000 claims description 43
229910052799 carbon Inorganic materials 0.000 claims description 40
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 39
125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 35
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 35
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 32
125000001425 triazolyl group Chemical group 0.000 claims description 29
239000004480 active ingredient Substances 0.000 claims description 27
125000000217 alkyl group Chemical group 0.000 claims description 27
125000002883 imidazolyl group Chemical group 0.000 claims description 26
229910052760 oxygen Inorganic materials 0.000 claims description 26
125000001072 heteroaryl group Chemical group 0.000 claims description 24
239000001301 oxygen Substances 0.000 claims description 24
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 23
150000001721 carbon Chemical group 0.000 claims description 22
201000010099 disease Diseases 0.000 claims description 22
244000038559 crop plants Species 0.000 claims description 18
239000000463 material Substances 0.000 claims description 18
125000001309 chloro group Chemical group Cl* 0.000 claims description 17
125000001153 fluoro group Chemical group F* 0.000 claims description 17
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 16
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 15
125000005843 halogen group Chemical group 0.000 claims description 15
125000004433 nitrogen atom Chemical group N* 0.000 claims description 13
229910052717 sulfur Inorganic materials 0.000 claims description 12
239000011593 sulfur Substances 0.000 claims description 12
125000000335 thiazolyl group Chemical group 0.000 claims description 12
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 11
150000002431 hydrogen Chemical class 0.000 claims description 11
229910052757 nitrogen Inorganic materials 0.000 claims description 11
125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims description 10
125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 9
125000003545 alkoxy group Chemical group 0.000 claims description 9
125000004076 pyridyl group Chemical group 0.000 claims description 9
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125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 6
125000001188 haloalkyl group Chemical group 0.000 claims description 6
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 6
150000003839 salts Chemical class 0.000 claims description 6
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125000003943 azolyl group Chemical group 0.000 claims description 5
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 5
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125000006273 (C1-C3) alkyl group Chemical group 0.000 claims description 3
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 3
125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 3
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125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 3
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125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 3
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 3
125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 3
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 3
125000004122 cyclic group Chemical group 0.000 claims description 2
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229910002651 NO3 Inorganic materials 0.000 claims 1
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238000002360 preparation method Methods 0.000 abstract description 10
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