JP2015525242A - 殺菌・殺カビ性4−メチルアニリノピラゾール - Google Patents
殺菌・殺カビ性4−メチルアニリノピラゾール Download PDFInfo
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- JP2015525242A JP2015525242A JP2015518504A JP2015518504A JP2015525242A JP 2015525242 A JP2015525242 A JP 2015525242A JP 2015518504 A JP2015518504 A JP 2015518504A JP 2015518504 A JP2015518504 A JP 2015518504A JP 2015525242 A JP2015525242 A JP 2015525242A
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- Prior art keywords
- fungicides
- compound
- dimethyl
- amine
- pyrazol
- Prior art date
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- 230000000855 fungicidal effect Effects 0.000 title claims abstract description 163
- 230000000844 anti-bacterial effect Effects 0.000 title claims description 160
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- 238000000034 method Methods 0.000 claims abstract description 70
- 229910052794 bromium Inorganic materials 0.000 claims abstract description 41
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 40
- 150000003839 salts Chemical class 0.000 claims abstract description 37
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- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 38
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- DOMXUEMWDBAQBQ-WEVVVXLNSA-N terbinafine Chemical compound C1=CC=C2C(CN(C\C=C\C#CC(C)(C)C)C)=CC=CC2=C1 DOMXUEMWDBAQBQ-WEVVVXLNSA-N 0.000 description 1
- 229960002722 terbinafine Drugs 0.000 description 1
- URHWNXDZOULUHC-UHFFFAOYSA-N tert-butyl n-[6-[[[(1-methyltetrazol-5-yl)-phenylmethylidene]amino]oxymethyl]pyridin-2-yl]carbamate Chemical compound CN1N=NN=C1C(C=1C=CC=CC=1)=NOCC1=CC=CC(NC(=O)OC(C)(C)C)=N1 URHWNXDZOULUHC-UHFFFAOYSA-N 0.000 description 1
- IOGXOCVLYRDXLW-UHFFFAOYSA-N tert-butyl nitrite Chemical compound CC(C)(C)ON=O IOGXOCVLYRDXLW-UHFFFAOYSA-N 0.000 description 1
- 239000012414 tert-butyl nitrite Substances 0.000 description 1
- BSYVTEYKTMYBMK-UHFFFAOYSA-N tetrahydrofurfuryl alcohol Chemical compound OCC1CCCO1 BSYVTEYKTMYBMK-UHFFFAOYSA-N 0.000 description 1
- 229960005199 tetramethrin Drugs 0.000 description 1
- 150000003536 tetrazoles Chemical class 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 125000004305 thiazinyl group Chemical group S1NC(=CC=C1)* 0.000 description 1
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- QSOHVSNIQHGFJU-UHFFFAOYSA-L thiosultap disodium Chemical compound [Na+].[Na+].[O-]S(=O)(=O)SCC(N(C)C)CSS([O-])(=O)=O QSOHVSNIQHGFJU-UHFFFAOYSA-L 0.000 description 1
- 230000009974 thixotropic effect Effects 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 235000010215 titanium dioxide Nutrition 0.000 description 1
- WPALTCMYPARVNV-UHFFFAOYSA-N tolfenpyrad Chemical compound CCC1=NN(C)C(C(=O)NCC=2C=CC(OC=3C=CC(C)=CC=3)=CC=2)=C1Cl WPALTCMYPARVNV-UHFFFAOYSA-N 0.000 description 1
- RSOBJVBYZCMJOS-CYBMUJFWSA-N tolprocarb Chemical group FC(F)(F)COC(=O)N[C@@H](C(C)C)CNC(=O)C1=CC=C(C)C=C1 RSOBJVBYZCMJOS-CYBMUJFWSA-N 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-M toluene-4-sulfonate Chemical compound CC1=CC=C(S([O-])(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-M 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 239000003053 toxin Substances 0.000 description 1
- 231100000765 toxin Toxicity 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 230000005945 translocation Effects 0.000 description 1
- 229960002622 triacetin Drugs 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- BAZVSMNPJJMILC-UHFFFAOYSA-N triadimenol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC1=CC=C(Cl)C=C1 BAZVSMNPJJMILC-UHFFFAOYSA-N 0.000 description 1
- YWBFPKPWMSWWEA-UHFFFAOYSA-O triazolopyrimidine Chemical compound BrC1=CC=CC(C=2N=C3N=CN[N+]3=C(NCC=3C=CN=CC=3)C=2)=C1 YWBFPKPWMSWWEA-UHFFFAOYSA-O 0.000 description 1
- DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-UHFFFAOYSA-N 0.000 description 1
- ZDRNMODJXFOYMN-UHFFFAOYSA-N tridecyl acetate Chemical compound CCCCCCCCCCCCCOC(C)=O ZDRNMODJXFOYMN-UHFFFAOYSA-N 0.000 description 1
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- ITMCEJHCFYSIIV-UHFFFAOYSA-M triflate Chemical compound [O-]S(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-M 0.000 description 1
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
- WVLBCYQITXONBZ-UHFFFAOYSA-N trimethyl phosphate Chemical compound COP(=O)(OC)OC WVLBCYQITXONBZ-UHFFFAOYSA-N 0.000 description 1
- 238000001665 trituration Methods 0.000 description 1
- 108010013280 ubiquinol oxidase Proteins 0.000 description 1
- 241000701447 unidentified baculovirus Species 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- DRTQHJPVMGBUCF-UHFFFAOYSA-N uracil arabinoside Natural products OC1C(O)C(CO)OC1N1C(=O)NC(=O)C=C1 DRTQHJPVMGBUCF-UHFFFAOYSA-N 0.000 description 1
- 229940045145 uridine Drugs 0.000 description 1
- 229940070710 valerate Drugs 0.000 description 1
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- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 238000011179 visual inspection Methods 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000004562 water dispersible granule Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
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- 239000005943 zeta-Cypermethrin Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 235000014692 zinc oxide Nutrition 0.000 description 1
- PQHXFGUTAAIHOC-XZZSYSLUSA-N α-(methoxyimino)-n-methyl-2-[[[1-[3-(trifluoromethyl)phenyl]ethoxy]imino]methyl]benzeneacetamide Chemical compound CNC(=O)C(=N\OC)\C1=CC=CC=C1\C=N\OC(C)C1=CC=CC(C(F)(F)F)=C1 PQHXFGUTAAIHOC-XZZSYSLUSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/38—Nitrogen 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
R1はF、ClまたはBrであり;
R2は、H、F、ClまたはBrであり;および
R3は、F、ClまたはBrである)
R1はF、ClまたはBrであり;
R2は、H、F、ClまたはBrであり;
R3は、F、ClまたはBrであり;および
R32は、H、CH3、CH2CH3または(CH2)2CH3である)
OCH2CH2が挙げられる。「アルコキシアルコキシ」はアルコキシにおけるアルコキシ置換を示す。「アルキルチオ」は、メチルチオ、エチルチオなどの分岐または直鎖アルキルチオ部分、ならびに、異なるプロピルチオ、ブチルチオ、ペンチルチオおよびヘキシルチオ異性体を含む。「アルキルチオアルキル」は、アルキルにおけるアルキルチオ置換を示す。「アルキルチオアルキル」の例としては、CH3SCH2、CH3SCH2CH2、CH3CH2SCH2、CH3CH2CH2CH2SCH2およびCH3CH2SCH2CH2が挙げられる。「アルコキシアルキル」は、アルコキシ部分におけるアルキル置換を示す。例としては、CH3CH2CH2OCH2−およびCH3CH2OCH2CH2−が挙げられる。「アルコキシアルケニル」および「アルコキシアルキニル」は、それぞれ、アルコキシ部分におけるアルケニルおよびアルキニル置換を示す。「アルコキシアルケニル」の例としては、CH2=CH2CH2OCH2およびCH2=CH2CH2OCH2CH2が挙げられる。「アルコキシアルキニル」の例としては、CH≡CHCH2OCH2およびCH≡CHCH2OCH2CH2が挙げられる。
実施形態A1.発明の概要に記載の式1の化合物。
(b1)メチルベンズイミダゾールカルバメート(MBC)殺菌・殺カビ剤;
(b2)ジカルボキシイミド殺菌・殺カビ剤;
(b3)脱メチル化抑制剤(DMI)殺菌・殺カビ剤;
(b4)フェニルアミド殺菌・殺カビ剤;
(b5)アミン/モルホリン殺菌・殺カビ剤;
(b6)リン脂質生合成抑制剤殺菌・殺カビ剤;
(b7)カルボキサミド殺菌・殺カビ剤;
(b8)ヒドロキシ(2−アミノ−)ピリミジン殺菌・殺カビ剤;
(b9)アニリノピリミジン殺菌・殺カビ剤;
(b10)N−フェニルカルバメート殺菌・殺カビ剤;
(b11)キノン外部抑制剤(QoI)殺菌・殺カビ剤;
(b12)フェニルピロール殺菌・殺カビ剤;
(b13)キノリン殺菌・殺カビ剤;
(b14)脂質過酸化抑制剤殺菌・殺カビ剤;
(b15)メラニン生合成抑制剤−レダクターゼ(MBI−R)殺菌・殺カビ剤;
(b16)メラニン生合成抑制剤−デヒドラターゼ(MBI−D)殺菌・殺カビ剤;
(b17)ヒドロキシアニリド殺菌・殺カビ剤;
(b18)スクアレン−エポキシダーゼ抑制剤殺菌・殺カビ剤;
(b19)ポリオキシン殺菌・殺カビ剤;
(b20)フェニル尿素殺菌・殺カビ剤;
(b21)キノン内部抑制剤(QiI)殺菌・殺カビ剤;
(b22)ベンズアミド殺菌・殺カビ剤;
(b23)エノピラヌロン酸抗生物質殺菌・殺カビ剤;
(b24)ヘキソピラノシル抗生物質殺菌・殺カビ剤;
(b25)グルコピラノシル抗生物質:タンパク質合成殺菌・殺カビ剤;
(b26)グルコピラノシル抗生物質:トレハラーゼおよびイノシトール生合成殺菌・殺カビ剤;
(b27)シアノアセタミドオキシム殺菌・殺カビ剤;
(b28)カルバメート殺菌・殺カビ剤;
(b29)酸化性リン酸化脱共役殺菌・殺カビ剤;
(b30)有機錫殺菌・殺カビ剤;
(b31)カルボン酸殺菌・殺カビ剤;
(b32)芳香族複素環式殺菌・殺カビ剤;
(b33)ホスホネート殺菌・殺カビ剤;
(b34)フタルアミド酸殺菌・殺カビ剤;
(b35)ベンゾトリアジン殺菌・殺カビ剤;
(b36)ベンゼン−スルホンアミド殺菌・殺カビ剤;
(b37)ピリダジノン殺菌・殺カビ剤;
(b38)チオフェン−カルボキサミド殺菌・殺カビ剤;
(b39)ピリミジンアミド殺菌・殺カビ剤;
(b40)カルボン酸アミド(CAA)殺菌・殺カビ剤;
(b41)テトラサイクリン抗生物質殺菌・殺カビ剤;
(b42)チオカルバメート殺菌・殺カビ剤;
(b43)ベンズアミド殺菌・殺カビ剤;
(b44)宿主植物防御誘起殺菌・殺カビ剤;
(b45)多部位接触作用殺菌・殺カビ剤;
(b46)コンポーネント(a)およびコンポーネント(b1)〜(b45)の殺菌・殺カビ剤以外の殺菌・殺カビ剤;および
(b1)〜(b46)の化合物の塩
からなる群から選択される少なくとも1種の殺菌・殺カビ性化合物を含む。
などの(b46)コンポーネント(a)およびコンポーネント(b1)〜(b45)の殺菌・殺カビ剤以外の殺菌・殺カビ剤から選択される少なくとも1種の化合物を含む。
などの(b46)コンポーネント(a)およびコンポーネント(b1)〜(b45)の殺菌・殺カビ剤以外の殺菌・殺カビ剤から選択される少なくとも1種の化合物を含む。
などの(b46)コンポーネント(a)およびコンポーネント(b1)〜(b45)の殺菌・殺カビ剤以外の殺菌・殺カビ剤から選択される少なくとも1種の化合物を含む。
Rb8は、ハロゲン、C1〜C4アルコキシまたはC2〜C4アルキニルであり;
Rb9は、H、ハロゲンまたはC1〜C4アルキルであり;
Rb10は、C1〜C12アルキル、C1〜C12ハロアルキル、C1〜C12アルコキシ、C2〜C12アルコキシアルキル、C2〜C12アルケニル、C2〜C12アルキニル、C4〜C12アルコキシアルケニル、C4〜C12アルコキシアルキニル、C1〜C12アルキルチオまたはC2〜C12アルキルチオアルキルであり;
Rb11はメチルまたは−Yb13−Rb12であり;
Rb12はC1〜C2アルキルであり;および
Yb13はCH2、OまたはSである)
などの(b46)コンポーネント(a)およびコンポーネント(b1)〜(b45)の殺菌・殺カビ剤以外の殺菌・殺カビ剤から選択される少なくとも1種の化合物を含む。
からなる群から選択される少なくとも1種の殺菌・殺カビ性化合物を含む。
からなる群から選択される少なくとも1種の殺菌・殺カビ性化合物を含む。
(c1)メチルベンズイミダゾールカルバメート(MBC)殺菌・殺カビ剤;
(c2)ジカルボキシイミド殺菌・殺カビ剤;
(c3)脱メチル化抑制剤(DMI)殺菌・殺カビ剤;
(c4)フェニルアミド殺菌・殺カビ剤;
(c5)アミン/モルホリン殺菌・殺カビ剤;
(c6)リン脂質生合成抑制剤殺菌・殺カビ剤;
(c7)カルボキサミド殺菌・殺カビ剤;
(c8)ヒドロキシ(2−アミノ−)ピリミジン殺菌・殺カビ剤;
(c9)アニリノピリミジン殺菌・殺カビ剤;
(c10)N−フェニルカルバメート殺菌・殺カビ剤;
(c11)キノン外部抑制剤(QoI)殺菌・殺カビ剤;
(c12)フェニルピロール殺菌・殺カビ剤;
(c13)キノリン殺菌・殺カビ剤;
(c14)脂質過酸化抑制剤殺菌・殺カビ剤;
(c15)メラニン生合成抑制剤−レダクターゼ(MBI−R)殺菌・殺カビ剤;
(c16)メラニン生合成抑制剤−デヒドラターゼ(MBI−D)殺菌・殺カビ剤;
(c17)ヒドロキシアニリド殺菌・殺カビ剤;
(c18)スクアレン−エポキシダーゼ抑制剤殺菌・殺カビ剤;
(c19)ポリオキシン殺菌・殺カビ剤;
(c20)フェニル尿素殺菌・殺カビ剤;
(c21)キノン内部抑制剤(QiI)殺菌・殺カビ剤;
(c22)ベンズアミド殺菌・殺カビ剤;
(c23)エノピラヌロン酸抗生物質殺菌・殺カビ剤;
(c24)ヘキソピラノシル抗生物質殺菌・殺カビ剤;
(c25)グルコピラノシル抗生物質:タンパク質合成殺菌・殺カビ剤;
(c26)グルコピラノシル抗生物質:トレハラーゼおよびイノシトール生合成殺菌・殺カビ剤;
(c27)シアノアセタミドオキシム殺菌・殺カビ剤;
(c28)カルバメート殺菌・殺カビ剤;
(c29)酸化性リン酸化脱共役殺菌・殺カビ剤;
(c30)有機錫殺菌・殺カビ剤;
(c31)カルボン酸殺菌・殺カビ剤;
(c32)芳香族複素環式殺菌・殺カビ剤;
(c33)ホスホネート殺菌・殺カビ剤;
(c34)フタルアミド酸殺菌・殺カビ剤;
(c35)ベンゾトリアジン殺菌・殺カビ剤;
(c36)ベンゼン−スルホンアミド殺菌・殺カビ剤;
(c37)ピリダジノン殺菌・殺カビ剤;
(c38)チオフェン−カルボキサミド殺菌・殺カビ剤;
(c39)ピリミジンアミド殺菌・殺カビ剤;
(c40)カルボン酸アミド(CAA)殺菌・殺カビ剤;
(c41)テトラサイクリン抗生物質殺菌・殺カビ剤;
(c42)チオカルバメート殺菌・殺カビ剤;
(c43)ベンズアミド殺菌・殺カビ剤;
(c44)宿主植物防御誘起殺菌・殺カビ剤;
(c45)多部位接触作用殺菌・殺カビ剤;
(c46)コンポーネント(a)およびコンポーネント(c1)〜(c45)の殺菌・殺カビ剤以外の殺菌・殺カビ剤;ならびに
(c1)〜(c46)の化合物の塩
からなる群から選択される少なくとも1種の殺菌・殺カビ性化合物を含む。
実施形態1.式1の化合物であって、式中、
R1はFまたはClであり;および
R2は、F、ClまたはBrである。
R1はFであり;および
R2は、ClまたはBrである。
R2はBrであり;および
R3は、ClまたはBrである。
N−(2−ブロモ−6−フルオロ−4−メチルフェニル)−4−(2−クロロ−4−フルオロフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン(すなわち化合物1)、
4−(2−クロロ−4−フルオロフェニル)−N−(2−クロロ−4−メチルフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン(すなわち化合物2)、
N−(2−ブロモ−4−メチルフェニル)−4−(2−クロロ−4−フルオロフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン(すなわち化合物3)、
4−(2−ブロモ−4−フルオロフェニル)−N−(2−クロロ−4−メチルフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン(すなわち化合物4)、
4−(2−ブロモ−4−フルオロフェニル)−N−(2−ブロモ−4−メチルフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン(すなわち化合物5)、
4−(2−クロロ−4−フルオロフェニル)−N−(2−フルオロ−4−メチルフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン(すなわち化合物6)、
N−(2−ブロモ−6−フルオロ−4−メチルフェニル)−4−(2−ブロモ−4−フルオロフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン(すなわち化合物7)、
N−(2−ブロモ−6−フルオロ−4−メチルフェニル)−4−(2,4−ジフルオロフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン(すなわち化合物8)、
N−(2,6−ジフルオロ−4−メチルフェニル)−4−(2,4−ジフルオロフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン(すなわち化合物9)、
4−(2−クロロ−4−フルオロフェニル)−N−(2,6−ジフルオロ−4−メチルフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン(すなわち化合物10)、
4−(2−ブロモ−4−フルオロフェニル)−N−(2−クロロ−6−フルオロ−4−メチルフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン(すなわち化合物11)、
N−(2−クロロ−6−フルオロ−4−メチルフェニル)−4−(2−クロロ−4−フルオロフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン(すなわち化合物12)、
4−(2−クロロ−4−フルオロフェニル)−N−(2,6−ジクロロ−4−メチルフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン(すなわち化合物13)、
4−(2−ブロモ−4−フルオロフェニル)−N−(2,6−ジフルオロ−4−メチルフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン(すなわち化合物14)、
4−(2−ブロモ−4−フルオロフェニル)−N−(2,6−ジクロロ−4−メチルフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン(すなわち、化合物15)および
N−(2,6−ジクロロ−4−メチルフェニル)−4−(2,4−ジフルオロフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン(すなわち、化合物16)。
Heterocyclic Compounds 2005,41(1),105−110に記載されている。
ステップA:2−クロロ−6−フルオロ−4−メチルベンゼンアミンの調製(注記4−2)
4−ブロモ−2−クロロ−6−フルオロベンゼンアミン(1.00g、4.45mmol)の1,4−ジオキサン(15mL)中の溶液に、水(1.5mL)および炭酸セシウム(2.90g、8.91mmol)を添加し、次いで、混合物を表面下で窒素でスパージした。約5分間の後、2,4,6−トリメチルボロキシン(3.14mL、22.3mmol)および[1,1’−ビス)ジフェニルホスフィノ)フェロセン]ジクロロパラジウム(II)錯体をCH2Cl2(0.36g、0.44mmol)と一緒に添加し、混合物を窒素雰囲気下で撹拌し、還流で3時間加熱した。反応混合物を周囲温度に冷却させ、次いで、酢酸エチルで溶出しながら(約50mL)Celite(登録商標)珪藻土ろ過助剤1cmのパッドを通してろ過した。濾液を濃縮し、次いで、ヘキサン中の5%〜100%酢酸エチルの溶剤勾配を伴うシリカゲルによる中圧クロマトグラフィにより精製して、0.23gの表題の化合物を清透な明るい茶色の油として得た。
1H NMRδ6.87(s,1H),6.74(d,1H),3.90(br s,2H)2.22(s,3H)。
ステップA:1−クロロ−3−フルオロ−2−イソチオシアナト−5−メチルベンゼンの調製(注記3−2)
2−クロロ−6−フルオロ−4−メチルベンゼンアミン(すなわち、実施例1からの生成物)(0.23g、1.44mmol)をジクロロメタン(5mL)中に溶解した。炭酸カリウム(0.24g、1.7mmol)および水(5mL)を添加し、得られた混合物を、チオホスゲン(0.125mL、1.5mmol)のジクロロメタン(5mL)中の溶液を約5分間かけて滴下しながら、周囲温度で撹拌した。この混合物を周囲温度で16時間激しく攪拌し、次いで、追加の炭酸カリウム(0.60g、4.3mmol)、水(2mL)、チオホスゲン(0.083mL)およびジクロロメタン(2mL)を添加し、攪拌を16時間継続した。反応混合物を分割し、有機層を除去し、水性相をジクロロメタン(約20mL)で1回抽出した。有機相を組み合わせ、硫酸マグネシウムで乾燥させ、減圧下で濃縮した。得られた残渣を、ヘキサンとシリカゲルによる中圧クロマトグラフィにより精製して、0.050gの表題の化合物を清透な無色の油として得た。
1H NMRδ7.02(s,1H),6.85(d,1H),2.33(s,3H)。
ステップA:N−(2−ブロモ−6−フルオロ−4−メチルフェニル)−4−(2−クロロ−4−フルオロフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン(化合物1)の調製
カリウムtert−ブトキシド(テトラヒドロフラン中の1.0M溶液、4.46mL、4.46mmol)を無水テトラヒドロフラン(12mL)と組み合わせ、窒素雰囲気下で約0℃に冷却した(氷/アセトン浴)。2−クロロ−4−フルオロフェニルアセトン(0.75g、4.06mmol)の無水テトラヒドロフラン(約2mL)中の溶液を滴下し、反応混合物を約0℃でさらに1時間撹拌した。次いで、反応混合物をドライアイス/アセトン浴中で−20℃に冷却した。1−ブロモ−3−フルオロ−2−イソチオシアナト−5−メチルベンゼン(1.00g、4.06mmol)の無水テトラヒドロフラン(約2mL)中の溶液を滴下し、この混合物を−20〜−3℃で約30分間撹拌した。ヨードメタン(0.30mL、4.8mmol)の無水テトラヒドロフラン中の溶液を滴下し、得られた懸濁液を約5分間撹拌した。メチルヒドラジン(1.52mL、28.4mmol)および氷酢酸(0.7mL、12mmol)のメタノール(7mL)中の溶液を添加し、この混合物を還流で約2時間加熱し、次いで、周囲温度に冷却させ、16時間撹拌した。水酸化ナトリウム水溶液(3N、16mL)を反応混合物に添加し、次いで、揮発物を減圧下で除去した。得られた残渣を約50mLの酢酸エチルと約50mLの水との間で分割した。水性相を約25mLの酢酸エチルで2回抽出し、組み合わせた有機相を塩水溶液で洗浄し、硫酸マグネシウムで乾燥させ、濃縮した。得られた黄色の油をヘキサン中の5%〜100%酢酸エチルの溶剤勾配を伴うシリカゲルによる中圧クロマトグラフィにより精製して、所望の生成物を黄色の固体として得た。20%酢酸エチル/ヘキサンによる倍散で、0.49gの表題の化合物をオフホワイトの固体(m.p.136〜137℃)として得た。追加の収穫物(0.155g)を黄褐色の固体(m.p.132〜133℃)として得た。
1H NMRδ7.03〜7.08(m,2H),6.94(s,1H),6.82(m,1H),6.61(m,1H),5.32(br s,1H),3.77(s,3H),2.17(s,3H),2.10(s,3H);MS 428(AP+)。
ステップA:N−(2,6−ジフルオロ−4−メチルフェニル)−4−(2,4−ジフルオロフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン(化合物9)の調製
N−(4−ブロモ−2,6−ジフルオロフェニル)−4−(2,4−ジフルオロフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン(すなわち、国際公開第2010/101973 A1号パンフレットにおいて調製のとおり)(0.12g、0.29mmol)の1,4−ジオキサン(2mL)中の混合物に、炭酸セシウム(0.19g、0.57mmol)、水(4滴)および[1,1’−ビス)ジフェニルホスフィノ)フェロセン]ジクロロパラジウム(II)錯体をCH2Cl2(0.024g、0.29mmol)と一緒に添加し、この混合物を、5分間表面下で窒素でスパージした。2,4,6−トリメチルボロキシン(0.203mL、1.44mmol)を添加し、混合物を窒素雰囲気下で撹拌し、還流で3時間加熱した。周囲温度に冷却した後、反応混合物を、Celite(登録商標)珪藻土ろ過助剤1cmのパッドを通してろ過し、酢酸エチル(約25mL)で溶出した。濾液を濃縮し、次いで、ヘキサン中の5%〜100%酢酸エチルの溶剤勾配を伴うシリカゲルによる中圧クロマトグラフィにより精製して、0.081gの表題の化合物を白色の固体(m.p.156〜158℃)として得た。
1H NMRδ7.07(m,1H),6.70〜6.79(m,2H),6.52(m,2H),5.12(br s,NH),3.75(s,3H),2.18(s,3H),2.17(s,3H);MS 350(AP+)。
本発明の式1の化合物(そのN−オキシドおよび塩を含む)は、一般に、組成物、すなわち配合物において、キャリアとされる界面活性剤、固体希釈剤および液体希釈剤からなる群から選択される少なくとも1種の追加のコンポーネントと共に、殺菌・殺カビ性活性処方成分として用いられるであろう。配合物または組成物処方成分は、活性処方成分の物理特性、適用形態、ならびに、土壌タイプ、水分および温度などの環境要因と適合するよう選択される。
は、アルジモルフ、ドデモルフ、フェンプロピモルフ、トリデモルフおよびトリモルファミドが挙げられる。ピペリジンとしてはフェンプロピジンおよびピペラリンが挙げられる。スピロケタール−アミンとしてはスピロキサミンが挙げられる。
ロポキシ)−フェニル]−1−メチル−1H−ピラゾール−4−カルボキサミド(Registry Number 1172611−40−3)および(b46.7b)3−(ジフルオロメチル)−1−メチル−N−[2−(1,1,2,2−テトラフルオロエトキシ)フェニル]−1H−ピラゾール−4−カルボキサミド(Registry Number 923953−98−4)である。式46.7の化合物は、国際公開第2007/017450号パンフレットに記載の方法により調製可能である。
Rb8は、ハロゲン、C1〜C4アルコキシまたはC2〜C4アルキニルであり;
Rb9は、H、ハロゲンまたはC1〜C4アルキルであり;
Rb10は、C1〜C12アルキル、C1〜C12ハロアルキル、C1〜C12アルコキシ、C2〜C12アルコキシアルキル、C2〜C12アルケニル、C2〜C12アルキニル、C4〜C12アルコキシアルケニル、C4〜C12アルコキシアルキニル、C1〜C12アルキルチオまたはC2〜C12アルキルチオアルキルであり;
Rb11はメチルまたは−Yb13−Rb12であり;
Rb12はC1〜C2アルキルであり;および
Yb13はCH2、OまたはSである。
テストA〜H用テスト懸濁液の調製のための一般的なプロトコル:先ず、テスト化合物を最終体積の3%と等しい量でアセトン中に溶解し、次いで、250ppmの界面活性剤Trem(登録商標)014(多価アルコールエステル)を含有するアセトンおよび精製水(体積基準で50/50混合物)中に所望の濃度(ppm)で懸濁させた。次いで、得られたテスト懸濁液をテストA〜Fにおいて用いた。テスト植物への40ppmテスト懸濁液の流出点までの吹付けは、約160g/haの割合に等しかった。他に示されていない限りにおいて、格付値は、40ppmテスト懸濁液を用いたことを示す。
トマトの実生に流出点まで試験懸濁液を噴霧した。次の日に、実生に、ボトリチスシネレア(Botrytis cinerea)(トマトボトリチスの病因)の胞子懸濁液を播種し、飽和雰囲気中で20℃で48時間培養し、次いで、27℃のグロースチャンバーに3日間移し、その後、視覚的な病害の格付けを行った。
トマトの実生に流出点まで試験懸濁液を噴霧した。次の日に、実生に、アルタナリア ソラニ(Alternaria solani)(トマト夏疫病の病因)の胞子懸濁液を播種し、飽和雰囲気中で27℃で48時間培養し、次いで、24℃のグロースチャンバーに5日間移し、その後、視覚的な病害の格付けを行った。
テスト懸濁液をコムギ苗木に流出点まで噴霧した。次の日に、この苗木に、セプトリアノドルム(Septoria nodorum)(セプトリア(Septoria)ふ枯病の病因)の胞子懸濁液を播種し、飽和雰囲気中に20℃で48時間インキュベートし、次いで、20℃のグロースチャンバーに9日間移し、その後、視認による病害評価を行った。
コムギの実生に流出点まで試験懸濁液を噴霧した。次の日に、実生に、セプトリアトリティシ(Septoria tritici)(コムギ葉枯病の病因)の胞子懸濁液を播種し、飽和雰囲気中で24℃で48時間培養し、次いで、20℃のグロースチャンバーに19日間移し、その後、視覚的な病害の格付けを行った。
コムギ実生に、コムギ赤さび病菌(Puccinia recondita f. sp.tritici)(コムギ葉さび病の病因)の胞子懸濁液を播種し、飽和雰囲気中で20℃で24時間培養し、次いで、20℃のグロースチャンバーに2日間移した。2日後に、流出点まで試験懸濁液を噴霧し、次いで、実生を20℃のグロースチャンバーに4日間移した。移した後、視覚的な病害の格付けを行った。
コムギの実生に流出点まで試験懸濁液を噴霧した。次の日に、実生に、コムギ赤さび病菌(Puccinia recondita f. sp.tritici)(コムギ葉さび病の病因)の胞子懸濁液を播種し、飽和雰囲気中で20℃で24時間培養し、次いで、20℃のグロースチャンバーに7日間移し、その後、視覚的な病害の格付けを行った。
コムギの実生に流出点までテスト懸濁液を噴霧した。次の日に、実生に、ブルメリアグラニミス(Blumeria graminis f.sp.tritici)(コムギウドンコ病の病因であるエリシフェグラミニス(Erysiphe graminis f.sp.tritici)としても知られている)の芽胞粉剤を播種し、グロースチャンバー中で20℃で8日間インキュベートし、その後、病害評価を視覚的に行った。
Claims (8)
- R1がFまたはClであり;および
R2が、F、ClまたはBrである、
請求項1に記載の化合物。 - N−(2−ブロモ−6−フルオロ−4−メチルフェニル)−4−(2−クロロ−4−フルオロフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン、
4−(2−クロロ−4−フルオロフェニル)−N−(2−クロロ−4−メチルフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン、
N−(2−ブロモ−4−メチルフェニル)−4−(2−クロロ−4−フルオロフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン、
4−(2−ブロモ−4−フルオロフェニル)−N−(2−クロロ−4−メチルフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン、
4−(2−ブロモ−4−フルオロフェニル)−N−(2−ブロモ−4−メチルフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン、
4−(2−クロロ−4−フルオロフェニル)−N−(2−フルオロ−4−メチルフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン、
N−(2−ブロモ−6−フルオロ−4−メチルフェニル)−4−(2−ブロモ−4−フルオロフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン、
N−(2−ブロモ−6−フルオロ−4−メチルフェニル)−4−(2,4−ジフルオロフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン、
N−(2,6−ジフルオロ−4−メチルフェニル)−4−(2,4−ジフルオロフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン、
4−(2−クロロ−4−フルオロフェニル)−N−(2,6−ジフルオロ−4−メチルフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン、
4−(2−ブロモ−4−フルオロフェニル)−N−(2−クロロ−6−フルオロ−4−メチルフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミンおよび
N−(2−クロロ−6−フルオロ−4−メチルフェニル)−4−(2−クロロ−4−フルオロフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン
からなる群から選択される、請求項1に記載の化合物。 - N−(2−ブロモ−6−フルオロ−4−メチルフェニル)−4−(2−クロロ−4−フルオロフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン、
4−(2−クロロ−4−フルオロフェニル)−N−(2−クロロ−4−メチルフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン、
N−(2−ブロモ−4−メチルフェニル)−4−(2−クロロ−4−フルオロフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン、
4−(2−ブロモ−4−フルオロフェニル)−N−(2−クロロ−4−メチルフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン、
4−(2−ブロモ−4−フルオロフェニル)−N−(2−ブロモ−4−メチルフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン、
4−(2−クロロ−4−フルオロフェニル)−N−(2−フルオロ−4−メチルフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン、
N−(2−ブロモ−6−フルオロ−4−メチルフェニル)−4−(2−ブロモ−4−フルオロフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン、
N−(2−ブロモ−6−フルオロ−4−メチルフェニル)−4−(2,4−ジフルオロフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン、
N−(2,6−ジフルオロ−4−メチルフェニル)−4−(2,4−ジフルオロフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン、
4−(2−クロロ−4−フルオロフェニル)−N−(2,6−ジフルオロ−4−メチルフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン、
4−(2−ブロモ−4−フルオロフェニル)−N−(2−クロロ−6−フルオロ−4−メチルフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン、
N−(2−クロロ−6−フルオロ−4−メチルフェニル)−4−(2−クロロ−4−フルオロフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン、
4−(2−クロロ−4−フルオロフェニル)−N−(2,6−ジクロロ−4−メチルフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン、
4−(2−ブロモ−4−フルオロフェニル)−N−(2,6−ジフルオロ−4−メチルフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン、
4−(2−ブロモ−4−フルオロフェニル)−N−(2,6−ジクロロ−4−メチルフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミンおよび
N−(2,6−ジクロロ−4−メチルフェニル)−4−(2,4−ジフルオロフェニル)−1,3−ジメチル−1H−ピラゾール−5−アミン
からなる群から選択される、請求項1に記載の化合物。 - (a)請求項1に記載の化合物;および、(b)少なくとも1種の他の殺菌・殺カビ剤を含む、殺菌・殺カビ組成物。
- 成分(b)が:
(b1)メチルベンズイミダゾールカルバメート(MBC)殺菌・殺カビ剤;
(b2)ジカルボキシイミド殺菌・殺カビ剤;
(b3)脱メチル化抑制(DMI)殺菌・殺カビ剤;
(b4)フェニルアミド殺菌・殺カビ剤;
(b5)アミン/モルホリン殺菌・殺カビ剤;
(b6)リン脂質生合成抑制殺菌・殺カビ剤;
(b7)カルボキサミド殺菌・殺カビ剤;
(b8)ヒドロキシ(2−アミノ−)ピリミジン殺菌・殺カビ剤;
(b9)アニリノピリミジン殺菌・殺カビ剤;
(b10)N−フェニルカルバメート殺菌・殺カビ剤;
(b11)キノン外部抑制(QoI)殺菌・殺カビ剤;
(b12)フェニルピロール殺菌・殺カビ剤;
(b13)キノリン殺菌・殺カビ剤;
(b14)脂質過酸化抑制殺菌・殺カビ剤;
(b15)メラニン生合成抑制−レダクターゼ(MBI−R)殺菌・殺カビ剤;
(b16)メラニン生合成抑制−デヒドラターゼ(MBI−D)殺菌・殺カビ剤;
(b17)ヒドロキシアニリド殺菌・殺カビ剤;
(b18)スクアレン−エポキシダーゼ抑制殺菌・殺カビ剤;
(b19)ポリオキシン殺菌・殺カビ剤;
(b20)フェニル尿素殺菌・殺カビ剤;
(b21)キノン内部抑制(QiI)殺菌・殺カビ剤;
(b22)ベンズアミド殺菌・殺カビ剤;
(b23)エノピラヌロン酸抗菌殺菌・殺カビ剤;
(b24)ヘキソピラノシル抗菌殺菌・殺カビ剤;
(b25)グルコピラノシル抗菌:タンパク質合成性殺菌・殺カビ剤;
(b26)グルコピラノシル抗菌:トレハラーゼおよびイノシトール生合成性殺菌・殺カビ剤;
(b27)シアノアセタミドオキシム殺菌・殺カビ剤;
(b28)カルバメート殺菌・殺カビ剤;
(b29)酸化性リン酸化脱共役殺菌・殺カビ剤;
(b30)有機錫殺菌・殺カビ剤;
(b31)カルボン酸殺菌・殺カビ剤;
(b32)芳香族複素環式殺菌・殺カビ剤;
(b33)ホスホネート殺菌・殺カビ剤;
(b34)フタルアミド酸殺菌・殺カビ剤;
(b35)ベンゾトリアジン殺菌・殺カビ剤;
(b36)ベンゼン−スルホンアミド殺菌・殺カビ剤;
(b37)ピリダジノン殺菌・殺カビ剤;
(b38)チオフェン−カルボキサミド殺菌・殺カビ剤;
(b39)ピリミジンアミド殺菌・殺カビ剤;
(b40)カルボン酸アミド(CAA)殺菌・殺カビ剤;
(b41)テトラサイクリン抗菌殺菌・殺カビ剤;
(b42)チオカルバメート殺菌・殺カビ剤;
(b43)ベンズアミド殺菌・殺カビ剤;
(b44)宿主植物防護誘起殺菌・殺カビ剤;
(b45)多部位接触作用殺菌・殺カビ剤;
(b46)成分(a)および成分(b1)〜(b45)以外の殺菌・殺カビ剤;ならびに、(b1)〜(b46)の化合物の塩
からなる群から選択される少なくとも1種の殺菌・殺カビ性化合物を含む、請求項5に記載の殺菌・殺カビ組成物。 - 請求項6に記載の殺菌・殺カビ組成物;ならびに、界面活性剤、固体希釈剤および液体希釈剤からなる群から選択される少なくとも1種の追加のコンポーネント。
- 真菌性植物病原体により引き起こされる植物病害を防除する方法であって、前記植物もしくはその一部分または植物種子に、殺菌・殺カビ的に有効な量の請求項1に記載の化合物を適用するステップを含む方法。
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PCT/US2013/046220 WO2013192126A1 (en) | 2012-06-22 | 2013-06-18 | Fungicidal 4-methylanilino pyrazoles |
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TW201620879A (zh) * | 2014-04-28 | 2016-06-16 | 杜邦股份有限公司 | 除草性經取代之3-苯基-4-氟基苯甲醯基吡唑 |
WO2015171392A1 (en) | 2014-05-06 | 2015-11-12 | E. I. Du Pont De Nemours And Company | Fungicidal pyrazoles |
US10246420B2 (en) | 2014-07-24 | 2019-04-02 | Bayer Cropscience Aktiengesellschaft | Pyrazole derivatives |
CN107428694A (zh) | 2015-03-19 | 2017-12-01 | 杜邦公司 | 杀真菌吡唑 |
WO2018052838A1 (en) | 2016-09-16 | 2018-03-22 | E. I. Du Pont De Nemours And Company | Fungicidal pyrazoles |
TW202400547A (zh) * | 2018-09-06 | 2024-01-01 | 美商富曼西公司 | 殺真菌之經硝苯胺基取代之吡唑 |
CN110438521B (zh) * | 2019-07-15 | 2021-09-21 | 华南理工大学 | 一种电化学条件下n-甲基-n-(2-氰乙基)苯胺选择性脱甲基的方法 |
TW202200012A (zh) | 2020-03-11 | 2022-01-01 | 美商富曼西公司 | 殺真菌劑混合物 |
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MX2014015661A (es) | 2015-04-09 |
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