JP2001526187A5 - - Google Patents
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- Publication number
- JP2001526187A5 JP2001526187A5 JP2000524992A JP2000524992A JP2001526187A5 JP 2001526187 A5 JP2001526187 A5 JP 2001526187A5 JP 2000524992 A JP2000524992 A JP 2000524992A JP 2000524992 A JP2000524992 A JP 2000524992A JP 2001526187 A5 JP2001526187 A5 JP 2001526187A5
- Authority
- JP
- Japan
- Prior art keywords
- methyl
- group
- substituted
- phenyl
- triazol
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 13
- 239000000203 mixture Substances 0.000 description 13
- -1 amide compound Chemical class 0.000 description 12
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 11
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 10
- 229910052801 chlorine Inorganic materials 0.000 description 10
- 239000000460 chlorine Chemical group 0.000 description 10
- 230000000855 fungicidal effect Effects 0.000 description 10
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 10
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 description 9
- 239000000417 fungicide Substances 0.000 description 7
- 229910052736 halogen Inorganic materials 0.000 description 7
- 150000002367 halogens Chemical class 0.000 description 7
- 125000000217 alkyl group Chemical group 0.000 description 6
- 125000001424 substituent group Chemical group 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 5
- 241000233866 Fungi Species 0.000 description 4
- 125000003545 alkoxy group Chemical group 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- 125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 description 2
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 125000002723 alicyclic group Chemical group 0.000 description 2
- 125000004414 alkyl thio group Chemical group 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 125000004465 cycloalkenyloxy group Chemical group 0.000 description 2
- 125000000753 cycloalkyl group Chemical group 0.000 description 2
- BQYJATMQXGBDHF-UHFFFAOYSA-N difenoconazole Chemical compound O1C(C)COC1(C=1C(=CC(OC=2C=CC(Cl)=CC=2)=CC=1)Cl)CN1N=CN=C1 BQYJATMQXGBDHF-UHFFFAOYSA-N 0.000 description 2
- 125000004438 haloalkoxy group Chemical group 0.000 description 2
- 125000004995 haloalkylthio group Chemical group 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 125000005842 heteroatom Chemical group 0.000 description 2
- 229910052740 iodine Chemical group 0.000 description 2
- 239000011630 iodine Chemical group 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 description 1
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 description 1
- 125000003626 1,2,4-triazol-1-yl group Chemical group [*]N1N=C([H])N=C1[H] 0.000 description 1
- HTSGKJQDMSTCGS-UHFFFAOYSA-N 1,4-bis(4-chlorophenyl)-2-(4-methylphenyl)sulfonylbutane-1,4-dione Chemical compound C1=CC(C)=CC=C1S(=O)(=O)C(C(=O)C=1C=CC(Cl)=CC=1)CC(=O)C1=CC=C(Cl)C=C1 HTSGKJQDMSTCGS-UHFFFAOYSA-N 0.000 description 1
- JWUCHKBSVLQQCO-UHFFFAOYSA-N 1-(2-fluorophenyl)-1-(4-fluorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethanol Chemical compound C=1C=C(F)C=CC=1C(C=1C(=CC=CC=1)F)(O)CN1C=NC=N1 JWUCHKBSVLQQCO-UHFFFAOYSA-N 0.000 description 1
- LQDARGUHUSPFNL-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)-3-(1,1,2,2-tetrafluoroethoxy)propyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(COC(F)(F)C(F)F)CN1C=NC=N1 LQDARGUHUSPFNL-UHFFFAOYSA-N 0.000 description 1
- HZJKXKUJVSEEFU-UHFFFAOYSA-N 2-(4-chlorophenyl)-2-(1H-1,2,4-triazol-1-ylmethyl)hexanenitrile Chemical compound C=1C=C(Cl)C=CC=1C(CCCC)(C#N)CN1C=NC=N1 HZJKXKUJVSEEFU-UHFFFAOYSA-N 0.000 description 1
- UFNOUKDBUJZYDE-UHFFFAOYSA-N 2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1CC(O)(C=1C=CC(Cl)=CC=1)C(C)C1CC1 UFNOUKDBUJZYDE-UHFFFAOYSA-N 0.000 description 1
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 description 1
- RQDJADAKIFFEKQ-UHFFFAOYSA-N 4-(4-chlorophenyl)-2-phenyl-2-(1,2,4-triazol-1-ylmethyl)butanenitrile Chemical compound C1=CC(Cl)=CC=C1CCC(C=1C=CC=CC=1)(C#N)CN1N=CN=C1 RQDJADAKIFFEKQ-UHFFFAOYSA-N 0.000 description 1
- 125000004070 6 membered heterocyclic group Chemical group 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- DBTDEFJAFBUGPP-UHFFFAOYSA-N Methanethial Chemical group S=C DBTDEFJAFBUGPP-UHFFFAOYSA-N 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000003302 alkenyloxy group Chemical group 0.000 description 1
- 125000004644 alkyl sulfinyl group Chemical group 0.000 description 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 description 1
- 125000000304 alkynyl group Chemical group 0.000 description 1
- 125000005133 alkynyloxy group Chemical group 0.000 description 1
- 150000007980 azole derivatives Chemical class 0.000 description 1
- 150000003851 azoles Chemical class 0.000 description 1
- 125000000392 cycloalkenyl group Chemical group 0.000 description 1
- 125000000000 cycloalkoxy group Chemical group 0.000 description 1
- 125000005043 dihydropyranyl group Chemical group O1C(CCC=C1)* 0.000 description 1
- YUCFVHQCAFKDQG-UHFFFAOYSA-N fluoromethane Chemical compound F[CH] YUCFVHQCAFKDQG-UHFFFAOYSA-N 0.000 description 1
- IJJVMEJXYNJXOJ-UHFFFAOYSA-N fluquinconazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1N1C(=O)C2=CC(F)=CC=C2N=C1N1C=NC=N1 IJJVMEJXYNJXOJ-UHFFFAOYSA-N 0.000 description 1
- FQKUGOMFVDPBIZ-UHFFFAOYSA-N flusilazole Chemical compound C=1C=C(F)C=CC=1[Si](C=1C=CC(F)=CC=1)(C)CN1C=NC=N1 FQKUGOMFVDPBIZ-UHFFFAOYSA-N 0.000 description 1
- 230000002538 fungal effect Effects 0.000 description 1
- 125000002541 furyl group Chemical group 0.000 description 1
- 125000001188 haloalkyl group Chemical group 0.000 description 1
- 125000003392 indanyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000004304 oxazol-5-yl group Chemical group O1C=NC=C1* 0.000 description 1
- 125000002971 oxazolyl group Chemical group 0.000 description 1
- TVLSRXXIMLFWEO-UHFFFAOYSA-N prochloraz Chemical compound C1=CN=CN1C(=O)N(CCC)CCOC1=C(Cl)C=C(Cl)C=C1Cl TVLSRXXIMLFWEO-UHFFFAOYSA-N 0.000 description 1
- STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 description 1
- 125000003226 pyrazolyl group Chemical group 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
- 125000004495 thiazol-4-yl group Chemical group S1C=NC(=C1)* 0.000 description 1
- 125000004496 thiazol-5-yl group Chemical group S1C=NC=C1* 0.000 description 1
- 125000000335 thiazolyl group Chemical group 0.000 description 1
- HSMVPDGQOIQYSR-KGENOOAVSA-N triflumizole Chemical compound C1=CN=CN1C(/COCCC)=N/C1=CC=C(Cl)C=C1C(F)(F)F HSMVPDGQOIQYSR-KGENOOAVSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19756405.4 | 1997-12-18 | ||
| DE19756405 | 1997-12-18 | ||
| PCT/EP1998/008224 WO1999031979A1 (de) | 1997-12-18 | 1998-12-15 | Fungizide mischungen auf der basis von amidverbindungen und azolen |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2001526187A JP2001526187A (ja) | 2001-12-18 |
| JP2001526187A5 true JP2001526187A5 (enExample) | 2006-01-26 |
| JP4336454B2 JP4336454B2 (ja) | 2009-09-30 |
Family
ID=7852445
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000524992A Expired - Fee Related JP4336454B2 (ja) | 1997-12-18 | 1998-12-15 | アミド化合物およびアゾールを基礎とする殺菌剤混合物 |
Country Status (30)
| Country | Link |
|---|---|
| US (1) | US6350765B1 (enExample) |
| EP (1) | EP1047300B1 (enExample) |
| JP (1) | JP4336454B2 (enExample) |
| KR (1) | KR100536150B1 (enExample) |
| CN (1) | CN1206916C (enExample) |
| AR (1) | AR014140A1 (enExample) |
| AT (1) | ATE246876T1 (enExample) |
| AU (1) | AU750310B2 (enExample) |
| BR (1) | BR9813573B1 (enExample) |
| CA (1) | CA2313479C (enExample) |
| CO (1) | CO5040022A1 (enExample) |
| CZ (1) | CZ293009B6 (enExample) |
| DE (1) | DE59809299D1 (enExample) |
| DK (1) | DK1047300T3 (enExample) |
| EA (1) | EA003136B1 (enExample) |
| ES (1) | ES2204005T3 (enExample) |
| FR (1) | FR14C0004I2 (enExample) |
| HU (1) | HU228232B1 (enExample) |
| IL (2) | IL136470A0 (enExample) |
| LU (1) | LU91456I2 (enExample) |
| NL (1) | NL350026I2 (enExample) |
| NZ (1) | NZ505597A (enExample) |
| PL (1) | PL191225B1 (enExample) |
| PT (1) | PT1047300E (enExample) |
| SI (1) | SI1047300T1 (enExample) |
| SK (1) | SK284960B6 (enExample) |
| TW (1) | TW431861B (enExample) |
| UA (1) | UA65601C2 (enExample) |
| WO (1) | WO1999031979A1 (enExample) |
| ZA (1) | ZA9811557B (enExample) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1227235C (zh) * | 1999-12-09 | 2005-11-16 | 辛根塔参与股份公司 | 作为杀菌剂的吡唑羧酰胺和吡唑硫代羧酰胺 |
| ATE449537T1 (de) * | 2001-01-18 | 2009-12-15 | Basf Se | Fungizide mischungen aus benzophenonen und n- biphenylnikotinamiden |
| EA007780B1 (ru) * | 2001-09-25 | 2007-02-27 | Басф Акциенгезельшафт | Кристаллические гидраты производных анилида никотиновой кислоты |
| DE10250110A1 (de) * | 2002-10-28 | 2004-05-13 | Bayer Cropscience Ag | Thiazol-(bi)cycloalkyl-carboxanilide |
| DE10307751A1 (de) * | 2003-02-14 | 2004-08-26 | Basf Ag | Neue kristalline Modifikation des Anhydrates von Boscalid |
| DE10347090A1 (de) * | 2003-10-10 | 2005-05-04 | Bayer Cropscience Ag | Synergistische fungizide Wirkstoffkombinationen |
| PE20070409A1 (es) * | 2005-06-29 | 2007-05-07 | Basf Ag | Mezclas fungicidas con base en bifenilamidas de acido pirazolcarboxilico disustituidas en 2,4 |
| WO2007003540A1 (de) * | 2005-06-30 | 2007-01-11 | Basf Aktiengesellschaft | Fungizide mischungen auf der basis von 2,5-disubstituierten pyrazolcarbonsäurebiphenylamiden |
| WO2007003564A1 (de) * | 2005-07-01 | 2007-01-11 | Basf Aktiengesellschaft | Fungizide mischungen auf der basis von 3,5-disubstituierten pyrazolcarbonsäurebiphenylamiden |
| US20090042725A1 (en) * | 2005-07-01 | 2009-02-12 | Basf Aktiengesellschaft | Fungicidal Mixtures Based on 3,5-Disubstituted N-Biphenyl-Pyrazolcarboxamides |
| JP2009500375A (ja) * | 2005-07-06 | 2009-01-08 | ビーエーエスエフ ソシエタス・ヨーロピア | １−メチルピラゾール−４−イルカルボキシアニリド類から製造される殺菌剤混合物 |
| US20090123561A1 (en) * | 2005-07-14 | 2009-05-14 | Basf Aktiengeselllschaft | Fungicide mixtures based on 1-methyl-pyrazol-4-ylcarboxanilides |
| EP1813151A1 (de) * | 2006-01-26 | 2007-08-01 | BASF Aktiengesellschaft | Fungizide Mischungen auf der Basis von 1-Methyl-pyrazol-4-yl-carbonsäureaniliden |
| DE102005035300A1 (de) * | 2005-07-28 | 2007-02-01 | Bayer Cropscience Ag | Synergistische fungizide Wirkstoffkombinationen |
| MX2009003673A (es) * | 2006-10-04 | 2009-04-22 | Pfizer Prod Inc | Derivados de piridido[4,3-d]pirimidin-4(3h)-ona como antagonistas de los receptores de calcio. |
| JP2012025735A (ja) * | 2010-06-24 | 2012-02-09 | Sumitomo Chemical Co Ltd | 植物病害防除組成物及び植物病害防除方法 |
| CN102334480A (zh) * | 2010-07-23 | 2012-02-01 | 青岛奥迪斯生物科技有限公司 | 一种含有啶酰菌胺和氟环唑的杀菌组合物 |
| CN102428931B (zh) * | 2011-12-23 | 2013-09-18 | 江阴苏利化学股份有限公司 | 一种含有啶酰菌胺和三唑类杀菌剂的杀菌组合物 |
| JP2014015412A (ja) * | 2012-07-06 | 2014-01-30 | Sumika Green Co Ltd | 植物病害防除組成物及び植物病害の防除方法 |
| UA84331U (uk) * | 2013-08-09 | 2013-10-10 | Сергей Михайлович Зайчук | Котел твердопаливний водогрійний |
| WO2015180999A1 (en) * | 2014-05-27 | 2015-12-03 | Basf Se | Ternary mixtures comprising biopesticides and sdhi fungicides and azole-type fungicides |
| CN104119322B (zh) * | 2014-07-11 | 2016-05-18 | 北京迪尔乐农业高新技术研发中心 | 一种用于杀菌的三唑类化合物及其制备方法和应用 |
| CN106135265A (zh) * | 2015-04-13 | 2016-11-23 | 南京华洲药业有限公司 | 一种含啶酰菌胺和氟硅唑的杀菌组合物及其应用 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2176106A (en) * | 1985-06-05 | 1986-12-17 | Uniroyal Ltd | Fungicides comprising carboxamidothiazoles |
| IL78825A0 (en) | 1985-06-05 | 1986-09-30 | Uniroyal Ltd | Fungicidal compositions containing carboxamidothiazoles and a method for protecting plants utilizing same |
| DE4130298A1 (de) | 1991-09-12 | 1993-03-18 | Basf Ag | Fungizide mischungen |
| DE122005000047I2 (de) | 1993-09-24 | 2011-07-21 | Basf Se | Fungizide Mischungen. |
| DE4331416A1 (de) * | 1993-12-09 | 1995-06-14 | Bayer Ag | Verwendung von Phenylcarbonsäure-amiden als Kristallisationsinhibitoren |
| DE4437048A1 (de) | 1994-10-17 | 1996-04-18 | Bayer Ag | Fungizide Wirkstoffkombinationen |
| ATE184751T1 (de) | 1995-08-17 | 1999-10-15 | Basf Ag | Fungizide mischungen eines oximethercarbonsäureamids mit azolderivaten |
| TW349094B (en) * | 1995-09-05 | 1999-01-01 | Basf Ag | Compositions and methods for controlling harmful fungi |
| DE19615976A1 (de) * | 1996-04-22 | 1997-10-23 | Basf Ag | Mittel und Verfahren zur Bekämpfung von Schadpilzen |
-
1998
- 1998-12-14 TW TW087120726A patent/TW431861B/zh not_active IP Right Cessation
- 1998-12-15 KR KR10-2000-7006690A patent/KR100536150B1/ko not_active Expired - Lifetime
- 1998-12-15 EP EP98966337A patent/EP1047300B1/de not_active Expired - Lifetime
- 1998-12-15 EA EA200000676A patent/EA003136B1/ru not_active IP Right Cessation
- 1998-12-15 AT AT98966337T patent/ATE246876T1/de active
- 1998-12-15 BR BRPI9813573-2A patent/BR9813573B1/pt not_active IP Right Cessation
- 1998-12-15 WO PCT/EP1998/008224 patent/WO1999031979A1/de not_active Ceased
- 1998-12-15 DK DK98966337T patent/DK1047300T3/da active
- 1998-12-15 CZ CZ20002228A patent/CZ293009B6/cs not_active IP Right Cessation
- 1998-12-15 PT PT98966337T patent/PT1047300E/pt unknown
- 1998-12-15 NZ NZ505597A patent/NZ505597A/xx not_active IP Right Cessation
- 1998-12-15 ES ES98966337T patent/ES2204005T3/es not_active Expired - Lifetime
- 1998-12-15 DE DE59809299T patent/DE59809299D1/de not_active Expired - Lifetime
- 1998-12-15 PL PL341317A patent/PL191225B1/pl unknown
- 1998-12-15 CN CN98812313.4A patent/CN1206916C/zh not_active Expired - Lifetime
- 1998-12-15 US US09/581,796 patent/US6350765B1/en not_active Expired - Lifetime
- 1998-12-15 AU AU22731/99A patent/AU750310B2/en not_active Expired
- 1998-12-15 JP JP2000524992A patent/JP4336454B2/ja not_active Expired - Fee Related
- 1998-12-15 CA CA002313479A patent/CA2313479C/en not_active Expired - Lifetime
- 1998-12-15 UA UA2000074346A patent/UA65601C2/uk unknown
- 1998-12-15 IL IL13647098A patent/IL136470A0/xx active IP Right Grant
- 1998-12-15 SI SI9830543T patent/SI1047300T1/xx unknown
- 1998-12-15 HU HU0100732A patent/HU228232B1/hu not_active IP Right Cessation
- 1998-12-15 SK SK814-2000A patent/SK284960B6/sk not_active IP Right Cessation
- 1998-12-17 ZA ZA9811557A patent/ZA9811557B/xx unknown
- 1998-12-18 AR ARP980106486A patent/AR014140A1/es active IP Right Grant
- 1998-12-18 CO CO98075478A patent/CO5040022A1/es unknown
-
2000
- 2000-05-31 IL IL136470A patent/IL136470A/en not_active IP Right Cessation
-
2006
- 2006-02-08 NL NL350026C patent/NL350026I2/nl unknown
-
2008
- 2008-06-11 LU LU91456C patent/LU91456I2/fr unknown
-
2014
- 2014-01-17 FR FR14C0004C patent/FR14C0004I2/fr active Active
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