UA104293C2 - Thiadiazolyloxy-phenylamidines anduse thereof as fungicides - Google Patents

Info

Publication number

UA104293C2

UA104293C2 UAA201100889A UAA201100889A UA104293C2 UA 104293 C2 UA104293 C2 UA 104293C2 UA A201100889 A UAA201100889 A UA A201100889A UA A201100889 A UAA201100889 A UA A201100889A UA 104293 C2 UA104293 C2 UA 104293C2

Authority

UA

Ukraine

Prior art keywords

thiadiazol

ethyl

oxy

methyl

methylimidoformamide

Prior art date

2008-06-27

Links

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• 239000000417 fungicide Substances 0.000 title description 8
• -1 1-cyclopropyl-2-ethoxyethyl group Chemical group 0.000 claims description 164
• PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims description 71
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 54
• RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 51
• 125000004122 cyclic group Chemical group 0.000 claims description 36
• 239000001257 hydrogen Substances 0.000 claims description 30
• 229910052739 hydrogen Inorganic materials 0.000 claims description 30
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 23
• 229910052736 halogen Inorganic materials 0.000 claims description 21
• 150000002367 halogens Chemical class 0.000 claims description 21
• 125000004432 carbon atom Chemical group C* 0.000 claims description 17
• 150000003839 salts Chemical class 0.000 claims description 17
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 15
• 125000004429 atom Chemical group 0.000 claims description 14
• 150000002431 hydrogen Chemical class 0.000 claims description 13
• 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 12
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 11
• 229910052799 carbon Inorganic materials 0.000 claims description 9
• 229910052757 nitrogen Inorganic materials 0.000 claims description 5
• 125000001424 substituent group Chemical group 0.000 claims description 5
• 125000001113 thiadiazolyl group Chemical group 0.000 claims description 5
• ZHNUHDYFZUAESO-UHFFFAOYSA-N formamide Substances NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 claims description 4
• 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 4
• AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 claims description 2
• 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
• 229910052796 boron Inorganic materials 0.000 claims description 2
• 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 2
• 125000005936 piperidyl group Chemical group 0.000 claims description 2
• 125000003944 tolyl group Chemical group 0.000 claims description 2
• ITMCEJHCFYSIIV-UHFFFAOYSA-M triflate Chemical compound [O-]S(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-M 0.000 claims description 2
• 125000004433 nitrogen atom Chemical group N* 0.000 claims 3
• 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 2
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 2
• 125000001475 halogen functional group Chemical group 0.000 claims 1
• 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
• 125000000446 sulfanediyl group Chemical group *S* 0.000 claims 1
• JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 claims 1
• 238000000034 method Methods 0.000 abstract description 26
• 244000005700 microbiome Species 0.000 abstract description 26
• 150000001875 compounds Chemical class 0.000 abstract description 21
• 150000001409 amidines Chemical class 0.000 abstract description 17
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