JP2005523273A - 二置換チアゾリルカルボキシアニリドおよび殺微生物薬としてのそれらの使用 - Google Patents
二置換チアゾリルカルボキシアニリドおよび殺微生物薬としてのそれらの使用 Download PDFInfo
- Publication number
- JP2005523273A JP2005523273A JP2003565983A JP2003565983A JP2005523273A JP 2005523273 A JP2005523273 A JP 2005523273A JP 2003565983 A JP2003565983 A JP 2003565983A JP 2003565983 A JP2003565983 A JP 2003565983A JP 2005523273 A JP2005523273 A JP 2005523273A
- Authority
- JP
- Japan
- Prior art keywords
- formula
- thiazolylcarboxyanilide
- methyl
- following formula
- bromine
- 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
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- 229940124561 microbicide Drugs 0.000 title 1
- 238000000034 method Methods 0.000 claims abstract description 55
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- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 15
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- YWSCPYYRJXKUDB-KAKFPZCNSA-N tralomethrin Chemical compound CC1(C)[C@@H](C(Br)C(Br)(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 YWSCPYYRJXKUDB-KAKFPZCNSA-N 0.000 description 1
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- 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
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- IQGKIPDJXCAMSM-UHFFFAOYSA-N triazoxide Chemical compound N=1C2=CC=C(Cl)C=C2[N+]([O-])=NC=1N1C=CN=C1 IQGKIPDJXCAMSM-UHFFFAOYSA-N 0.000 description 1
- DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-UHFFFAOYSA-N 0.000 description 1
- WLPUWLXVBWGYMZ-UHFFFAOYSA-N tricyclohexylphosphine Chemical compound C1CCCCC1P(C1CCCCC1)C1CCCCC1 WLPUWLXVBWGYMZ-UHFFFAOYSA-N 0.000 description 1
- RXJKFRMDXUJTEX-UHFFFAOYSA-N triethylphosphine Chemical compound CCP(CC)CC RXJKFRMDXUJTEX-UHFFFAOYSA-N 0.000 description 1
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- 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
- XAIPTRIXGHTTNT-UHFFFAOYSA-N triflumuron Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC(=O)NC(=O)C1=CC=CC=C1Cl XAIPTRIXGHTTNT-UHFFFAOYSA-N 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 238000002211 ultraviolet spectrum Methods 0.000 description 1
- 241000701451 unidentified granulovirus Species 0.000 description 1
- 241000701366 unidentified nuclear polyhedrosis viruses Species 0.000 description 1
- JARYYMUOCXVXNK-CSLFJTBJSA-N validamycin A Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-CSLFJTBJSA-N 0.000 description 1
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- 239000005943 zeta-Cypermethrin Substances 0.000 description 1
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- 239000011701 zinc Substances 0.000 description 1
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 description 1
- JLYXXMFPNIAWKQ-UHFFFAOYSA-N γ Benzene hexachloride Chemical compound ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole 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
- C07D277/56—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
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Abstract
【化1】
Description
下記式(I):
R1およびR2は、互いに独立に、ハロゲン、シアノ、ニトロ、C1〜C6−アルキル、C2〜C6−アルケニル、C1〜C4−アルコキシ、C1〜C4−アルキルチオ、C1〜C4−アルキルスルホニル、C3〜C6−シクロアルキルを表すか、各々の場合において、ハロゲン原子を1から5個有するC1〜C4−ハロアルキル、C1〜C4−ハロアルコキシ、C1〜C4−ハロアルキルチオまたはC1〜C4−ハロアルキルスルホニルを表し、
さらに、R1およびR2は、互いにオルト配置にある場合には一緒に、場合によってはハロゲン置換またはC1〜C6−アルキル置換されているアルケニレンを表す)
の新規チアゾリルカルボキシアニリドを提供する。
a)下記式(II):
R1およびR2は、上で定義したとおりであり、
G1およびG2は、各々水素を表すか、一緒にテトラメチルエチレンを表す)
のボロン酸誘導体とを、触媒の存在下、適する場合には酸結合剤の存在下、および適する場合には希釈剤の存在下で反応させること、または
c)下記式(VI)
R1およびR2は、上で定義したとおりであり、および
X3は、臭素、ヨウ素またはトリフルオロメチルスルホニルオキシを表す)
のハロベンゼン誘導体とを、触媒の存在下、適する場合には酸結合剤の存在下、および適する場合には希釈剤の存在下で反応させること、
によって得られることが判明した。
さらに、R1およびR2が、互いにオルト配置にある場合には一緒に、場合によってはフッ素置換、塩素置換、臭素置換またはメチル置換されているブタジエニレンを表す、式(I)のチアゾリルカルボキシアニリドは、好ましい。
d)下記式(II):
e)下記式(II):
ザントモナス(Xanthomonas)種:例えば、イネ白葉枯病菌(Xanthomonas campestris pv.oryzae)など;
シュードモナス(Pseudomonas)種:例えば、斑点細菌病菌(Pseudomonas syringae pv.lachrymans)など;
エルウィニア(Erwinia)種:例えば、エルウィニア・アミロボーラ(Erwinia amylovora)など;
クサレカビ属(Pythium)種:例えば、ピシウム・ウルチマム(Pythium ultimum)など;
疫病菌(Phytophthora)種:例えば、ジャガイモ疫病菌(Phytophthora infestans)など;
シュードペロノスポラ属(Pseusoperonospora)種:例えば、褐斑病菌(Pseudoperonospora humuli)またはウリ科べと病菌(Pseudoperonospora cubensis)など;
タンジクツユカビ属(Plasmopara)種:例えば、ブドウべと病菌(Plasmopara viticola)など;
ブレミア(Bremia)種:例えば、レタスべと病菌(Bremia lactucae)など;
ツユカビ属(Peronospora)種:例えば、ペロノスポラ・ピシ(Peronospora pisi)またはペロノスポラ・ブラッシカ(P.brassicae)など;
ウドンコカビ属(Erysiphae)種:例えば、コムギうどんこ病菌(Erysiphae graminis)など;
スファエロセカ属(Sphaerotheca)種:例えば、キュウリうどんこ病菌(Sphaerotheca fuliginea)など;
ロドスフェラ属(Podosphaera)種:例えば、リンゴうどんこ病菌(Podosphaera leucotricha)など;
ベンチュリア属(Venturia)種:例えば、リンゴ黒星病菌(Venturia inaequalis)など;
ピレノフォラ属(Pyrenophora)種:例えば、網班病菌(Pyrenophora teres)または班葉病菌(P.graminea)
(分生子形:ドレクスレラ属(Drechslera)、別名:ヘルミントスポリウム属(Helminthosporium))など;
コリオボラス属(Cochliobolus)種:例えば、イネ科斑点病菌(Cochliobolus sativus)
(分生子形:ドレクスレラ属(Drechslera)、別名:ヘルミントスポリウム属(Helminthosporium))など;
ウロミケス属(Uromyces)種:例えば、さび菌(Uromyces appendiculatus)など;
プクキニア属(Puccinia)種:例えば、コムギ赤さび病菌(Puccinia recondita)など;
スクレロティニア属(Sclerotinia)種:例えば、菌核病菌(Sclerotinia sclerotiorum)など;
チレッティア(Tilletia)種:例えば、コムギなまぐさ黒穂病菌(Tilletia caries)など;
黒穂菌属(Ustilago)種:例えば、オオムギ、コムギ裸黒穂病菌(Ustilago nuda)またはエンバク裸黒穂病菌(Ustilago avenae)など;
ペリキュラリア(Pellicularia)種:例えば、ササキクモノコウヤクタケ(Pellicularia sasakii)など;
ピリキュラリア属(Pyricularia)種:例えば、イネいもち病菌(Pryicularia oryzae)など;
フザリウム属(Fusarium)種:例えば、フザリウム・セルモラム(Fusarium culmorum)など;
ボトリチス属(Botrytis)種:例えば、灰色かび病菌(Botrytis cinerea)など;
セプトリア属(Septoria)種:例えば、コムギふ枯病菌セプトリア・ノトラム(Septoria nodorum)など;
レプトスフェリア属(Leptosphaeria)種:例えば、コムギふ枯病菌レプトスフェリア−ノドラム(Leptosphaeria nodorum)など;
セルコスポラ属(Cercospora)種:例えば、セルコスポラ−カネッセンス(Cercospora canescens)など;
アルテルナリア属(Alternaria)種:例えば、アブラナ科黒斑病菌(Alternaria brassicae)など;および
シュードセルコスポレラ属(Pseudocercosporella)種:例えば、コムギ眼紋病菌(Pseudocercosporella herpotrichoides)など。
殺真菌薬:
アルジモルフ、アムプロピルホス、アムプロピルホス・カリウム、アンドプリム、アニラジン、アザコナゾール、アゾキシストロビン、
ベナラキシル、ベノダニル、ベノミル、ベンザマクリル、ベンザマクリル−イソブチル、ビアラホス、ビナパクリル、ビフェニル、ビタータノール、ブラスチシジン−S、ブロムコナゾール、ブピリメート、ブチオベート、
多硫化カルシウム、カルプロパミド、カプシマイシン、ダイホルタン、カプタン、カルベンダジム、カルボキシン、カルボン、キノメチオネート、クロベンチアゾン、クロルフェナゾール、クロロネブ、クロロピクリン、クロロサロニル、クロゾリネート、クロジラコム、クフラネブ、シモキサニル、シプロコナゾール、シプロジニル、シプロフラム、
デバカルブ、ジクロロフェン、ジクロブトラゾール、ジクロフルアニド、ジクロメジン、ジクロラン、ジエトフェンカルブ、ジフェノコナゾール、ジメチリモール、ジメトモルフ、ジニコナゾール、ジニコナゾール−M、ジノキャップ、ジフェニルアミン、ジピリチオン、ジタリムホス、ジチアノン、ドデモルフ、ドジン、ドラゾキソロン、
エジフェンホス、エポキシコナゾール、エタコナゾール、エチリモール、エトリジアゾール、
ファモキサドン、フェナパニル、フェナリモール、フェンブコナゾール、フェンフラム、フェンヘキサミド、フェニトロパン、フェンピクロニル、フェンプロピジン、フェンプロピモルフ、フェンチンアセテート、フェンチンヒドロキシド、フェルバム、フェリムゾン、フルアジナム、フルメトーバー、フルオロマイド、フルキンコナゾール、フルルプリミドール、フルシラゾール、フルスルファミド、フルトラニル、フルトリアホール、ホルペット、ホセチル−アルミニウム、ホセチル−ナトリウム、フサライド、フベリダゾール、フララキシル、フラメトピル、フルカルボニル、フルコナゾール、フルコナゾール−cis、フルメシクロクス、
グアザチン、ヘキサクロロベンゼン、ヘキサコナゾール、ヒメキサゾール、
イマザリル、イミベンコナゾール、イミノオクタジン、イミノオクタジンアルベシレート、イミノクタジントリアセテート、ヨードカルブ、イプコナゾール、イプロベンホス(IBP)、イプロジオン、イプロバリカルブ、イルママイシン、イソプロチオラン、イソバレジオン、
カスガマイシン、クレソキシム−メチル、銅調製物(水酸化銅、ナフテン酸銅、オキシ塩化銅、硫酸銅、酸化銅、オキシン−銅およびボルドー合剤など)、
マンコッパー、マンコゼブ、マネブ、メフェリムゾン、メパニピリム、メプロニル、メタラキシル、メトコナゾール、メタスルホカルブ、メトフロキサム、メチラム、メトメクラム、メトスルホバクス、ミルジオマイシン、ミクロブタニル、マイクロゾリン、
ジメチルジチオカルバミン酸ニッケル、ニトロサール−イソプロピル、ヌアリモール、
オフラース、オキサジキシル、オキサモカルブ、オキソリン酸、オキシカルボキシム、オキシフェンチン、
パクロブトラゾール、ペフラゾエート、ペンコナゾール、ペンシクロン、ホスジフェン、ピコキシストロビン、ピマリシン、ピペラリン、ポリオキシン、ポリオキソリム、プロベナゾール、プロクロラズ、プロシミドン、プロパモカルブ、プロパノシン−ナトリウム、プロピコナゾール、プロピネブ、ピラクロストロビン、ピラゾホス、ピリフェノックス、ピリメタニル、ピロキロン、ピロキシフル、
キンコナゾール、キントゼン(PCNB)、キノキシフェン、
硫黄および硫黄調製物、スピロキサミン、
テブコナゾール、テクロフタラム、テクナゼン、テトシクラシス、テトラコナゾール、チアベンダゾール、チシオフェン、チフルザミド、チオファネート−メチル、チラム、チオキシミド、トルクロホス−メチル、トリルフルアニド、トリアジメホン、トリアジメノール、トリアズブチル、トリアゾキシド、トリクラミド、トリシクラゾール、トリデモルフ、トリフロキシストロビン、トリフルミゾール、トリホリン、トリチコナゾール、
ユニコナゾール、
バリダマイシン A、ビンクロゾリン、ビンコナゾール、
ザリルアミド、ジネブ、ジラム、ならびにまた
Dagger G、OK―8705、OK―8801、
α−(1,1−ジメチルエチル)−β−(2−フェノキシエチル)−1H−1,2,4−トリアゾール−1−エタノール、
α−(2,4−ジクロロフェニル)−β−フルオロ−β−プロピル−1H−1,2,4−トリアゾール−1−エタノール、
α−(2,4−ジクロロフェニル)−β−メトキシ−α−メチル−1H−1,2,4−トリアゾール−1−エタノール、
α―(5−メチル−1,3−ジオキサン−5−イル)−β−[[4−(トリフルオロメチル)−フェニル]−メチレン]―1H−1,2,4−トリアゾール−1−エタノール、
(5RS,6RS)−6−ヒドロキシ−2,2,7,7−テトラメチル−5−(1H−1,2,4−トリアゾール−1−イル)−3−オクタノン、
(E)−α−(メトキシイミノ)−N−メチル−2−フェノキシ−フェニルアセトアミド、
1−(2,4−ジクロロフェニル)−2−(1H−1,2,4−トリアゾール−1−イル)−エタノン−O−(フェニルメチル)−オキシム、
1−(2−メチル−1−ナフタレニル)−1H−ピロール−2,5−ジオン、
1−(3,5−ジクロロフェニル)−3−(2−プロペニル)−2,5−ピロリジンジオン、
1−[(ジヨードメチル)−スルホニル]−4−メチル−ベンゼン、
1−[[2―(2,4−ジクロロフェニル)−1,3−ジオキソラン−2−イル]−メチル−1H−イミダゾール、
1−[[2−(4−クロロフェニル)−3−フェニルオキシラニル]−メチル]−1H−1,2,4−トリアゾール、
1−[1−[2−[(2,4−ジクロロフェニル)−メトキシ]−フェニル]−エテニル]−1H−イミダゾール、
1−メチル−5−ノニル−2−(フェニルメチル)−3−ピロリジノール、
2’,6’−ジブロモ−2−メチル−4’−トリフルオロメトキシ−4’−トリフルオロ−メチル−1,3−チアゾール−5−カルボキサニリド、
2,6−ジクロロ−5−(メチルチオ)−4−ピリミジニル−チオシアネート、
2,6−ジクロロ−N−(4−トリフルオロメチルベンジル)−ベンズアミド、
2,6−ジクロロ−N−[[4−(トリフルオロメチル)−フェニル]−メチル]−ベンズアミド、
2−(2,3,3−トリヨード−2−プロペニル)−2H−テトラゾール、
2−[(1−メチルエチル)−スルホニル]−5−(トリクロロメチル)−1,3,4−チアジアゾール、
2−[[6−デオキシ−4−O−(4−O−メチル−β−D−グリコピラノシル)−α−D−グリコピラノシル]−アミノ]−4−メトキシ−1H−ピロロ[2,3−d]ピリミジン−5−カルボニトリル、
2−アミノブタン、
2−ブロモ−2−(ブロモメチル)−ペンタンジニトリル、
2−クロロ−N−(2,3−ジヒドロ−1,1,3−トリメチル−1H−インデン−4−イル)−3‐ピリジンカルボキサミド、
2−クロロ−N−(2,6−ジメチルフェニル)−N−(イソチオシアナトメチル)−アセトアミド、
2−フェニルフェノール(OPP)、
3,4−ジクロロ−1−[4−(ジフルオロメトキシ)−フェニル]−1H−ピロール−2,5−ジオン、
3,5−ジクロロ−N−[シアノ(1−メチル−2−プロピニル)−オキシ]−メチル]−ベンズアミド、
3−(1,1−ジメチルプロピル−1−オキソ−1H−インデン−2−カルボニトリル、
3−[2−(4−クロロフェニル)−5−エトキシ−3−イソキサゾリジニル]−ピリジン、
4−クロロ−2−シアノ−N,N−ジメチル−5−(4−メチルフェニル)−1H−イミダゾール−1−スルホンアミド、
4−メチル−テトラゾロ[1,5−a]キナゾリン−5(4H)−オン、
硫酸8−ヒドロキシキノリン、
9H−キサンテン−2−[(フェニルアミノ)−カルボニル]−9−カルボン酸ヒドラジド、
ビス−(1−メチルエチル)−3−メチル−4−[(3−メチルベンゾイル)−オキシ]−2,5−チオフェンジカルボキシレート、
cis−1−(4−クロロフェニル)−2−(1H−1,2,4−トリアゾール−1−イル)−シクロヘプタノール、
塩酸cis−4−[3−[4−(1,1−ジメチルプロピル)−フェニル−2−メチルプロピル]−2,6−ジメチル−モルホリン、
[(4−クロロフェニル)−アゾ]−シアノ酢酸エチル、
炭酸水素カリウム、
メタンテトラチオール・ナトリウム塩、
1−(2,3−ジヒドロ−2,2−ジメチル−1H−インデン−1−イル)−1H−イミダゾール−5−カルボン酸メチル、
N−(2,6−ジメチルフェニル)−N−(5−イソキサゾリルカルボニル)−DL−アラニン酸メチル、
N−(クロロアセチル)−N−(2,6−ジメチルフェニル)−DL−アラニン酸メチル、
N−(2,6−ジメチルフェニル)−2−メトキシ−N−(テトラヒドロ−2−オキソ−3−フラニル)−アセトアミド、
N−(2,6−ジメチルフェニル)−2−メトキシ−N−(テトラヒドロ−2−オキソ−3−チエニル)−アセトアミド、
N−(2−クロロ−4−ニトロフェニル)−4−メチル−3−ニトロ−ベンゼンスルホンアミド、
N−(4−シクロヘキシルフェニル)−1,4,5,6−テトラヒドロ−2−ピリミジンアミン、
N−(4−ヘキシルフェニル)−1,4,5,6−テトラヒドロ−2−ピリミジンアミン、
N−(5−クロロ−2−メチルフェニル)−2−メトキシ−N−(2−オキソ−3−オキサゾリジニル)−アセトアミド、
N−(6−メトキシ−3−ピリジニル)−シクロプロパンカルボキサミド、
N−[2,2,2−トリクロロ−1−[(クロロアセチル)−アミノ]−エチル]−ベンズアミド、
N−[3−クロロ−4,5−ビス−(2−プロピニルオキシ)−フェニル]−N’−メトキシ−メタンイミドアミド、
N−ホルミル−N−ヒドロキシ−DL−アラニン−ナトリウム塩、
[2−(ジプロピルアミノ)−2−オキソエチル]−エチルホスロアミドチオ酸O,O−ジエチル、
フェニルプロピルホスホロアミドチオ酸O−メチル S−フェニル、
1,2,3−ベンゾチアジアゾール−7−カルボチオ酸S−メチル、
スピロ[2H]−1−ベンゾピラン−2,1’(3’H)−イソベンゾフラン]−3’−オン、
4−[(3,4−ジメトキシフェニル)−3−(4−フルオロフェニル)−アクリロイル]−モルホリン。
ブロノポール、ジクロロフェン、ニトラピリン、ジメチルジチオカルバミン酸ニッケル、カスガマイシン、オクチリノン、フランカルボン酸、オキシテトラサイクリン、プロベナゾール、ストレプトマイシン、テクロフタラム、硫酸銅および他の銅調製物。
アバメクチン、アセフェート、アセトアミプリド、アクリナトリン、アラニカルブ、アルジカルブ、アルドキシカルブ、アルファシペルメトリン、アルファメトリン、アミトラズ、アベルメクチン、AZ 60541、アザジラクチン、アザメチホス、アジンホスA、アジンホスM、アゾシクロチン、
乳化病菌(Bacillus popilliae)、バシラス・スフェリカス(Bacillus sphaericus)、枯草菌(Bacillus subtilis)、バシラス・スリンジエンシス(Bacillus thuringiensis)、バキュロウイルス、ボーバリア・バッシアーナ(Beauvaria bassiana)、ボーバリア・テネーラ(Beauvaria tenella)、ベンジオカルブ、ベンフラカルブ、ベンスルタップ、ベンゾキシメート、ベータシフルトリン、ビフェナゼート、ビフェントリン、バイオエタノメトリン、バイオパーメトリン、ビストリフルロン、BPMC、ブロモホスA、ブフェンカルブ、ブプロフェジン、ブタチオホス、ブトカルボキシム、ブチルピリダベン、
カズサホス、カルバリル、カルボフラン、カルボフェノチオン、カルボスルファン、カルタップ、クロエトカルブ、クロルエトキシホス、クロルフェナピル、クロルフェンビンホス、クロルフルアズロン、クロルメホス、クロルピリホス、クロルピリホスM、クロバポルトリン、クロマフェノジド、cis−レスメトリン、cis−パーメトリン、クロシトリン、クロエトカルブ、クロフェンテジン、クロチアニジン、シアノホス、シクロプレン、シクロプロトリン、シフルトリン、シハロトリン、シヘキサチン、シパーメトリン、シロマジン、
デルタメトリン、デメトンM、デメトンS、デメトン−S−メチル、ジアフェンチウロン、ジアジノン、ジクロルボス、ジコホル、ジフルベンズウロン、ジメトエート、ジメチルビンホス、ジオフェノラン、ジスルホトン、ドクサット−ナトリウム、ドフェナピン、
エフルシラネート、エマメクチン、エムペントリン、エンドスルファン、ハエカビ属種(Entomophthora spp.)、エスフェンバレレート、エチオフェンカルブ、エチオン、エトプロホス、エトフェンプロックス、エトキサゾール、エトリムホス、
フェナミホス、フェナザキン、フェンブタチンオキシド、フェニトロチオン、フェノチオカルブ、フェノキサクリム、フェノキシカルブ、フェンプロパトリン、フェンピラド、フェンピリトリン、フェンピロキシメート、フェンバレレート、フィプロニル、フルアズロン、フルブロシトリネート、フルシクロキュロン、フルシトリネート、フルフェノキュロン、フルメトリン、フルテンジン、フルバリネート、ホノホス、ホスメチラン、ホスチアゼート、フブフェンプロックス、フラチオカルブ、
顆粒症ウイルス、
ハロフェノジド、HCH、ヘプテノホス、ヘキサフルムロン、ヘキシチアゾクス、ヒドロプレン、
イミダクロピリド、インドキサカルブ、イサゾホス、イソフェンホス、イソオキサチオン、イベルメクチン、
核多角体病ウイルス、
ラムダ−シハロトリン、ルフェヌロン、
マラチオン、メカルバム、メタアルデヒド、メタアミドホス、メサルヒジウム・アニソプリエ(Metharhizium anisopliae)、メサルヒジウム・フラボビリデ(Metharhizium flavoviride)、メチダチオン、メチオカルブ、メトプレン、メトミル、メトキシフェノジド、メトルカルブ、メトキサジアゾン、メビンホス、ミルベメクチン、ミルベマイシン、モノクロトホス、
ナレド、ニテンピラム、ニチアジン、ノバルロン、
オメトエート、オキサミル、オキシデメトンM、
ペシロマイセス・フモソルセウス(Paecilomyces fumosoroseus)、パラチオンA、パラチオンM、パーメトリン、フェントエート、ホレート、ホサロン、ホスメト、ホスファミドン、ホキシム、ピリミカルブ、ピリミホスA、ピリミホスM、プロフェノホス、プロメカルブ、プロパルギット、プロポスキル、プロチオホス、プロトエート、ピメトロジン、ピラクロホス、ピレスメトリン、ジョチュウギク、ピリダベン、ピリダチオン、ピリミジフェン、ピリプロキシフェン、
キナルホス、リバビリン、
サリチオン、セブホス、シラフルオフェン、スピノサド、スピロジクロフェン、スルホテプ、スルプロホス、
タウ−フルバリネート、テブフェノジド、テブフェンピラド、テブピリミホス、テフルベンズロン、テフルトリン、テメホス、テミビンホス、ターブホス、テトラクロルビンホス、テトラジホン、シータ−シペルメトリン、チアクロピリド、チアメトキサム、チアプロニル、チアトリホス、シュウ酸水素チオシクラム、チオジカルブ、チオファノックス、サーリンジエシン、トラロシトリン、トラロメトリン、トリアラテン、トリアザメート、トリアゾホス、トリアズロン、トリクロフェニジン、トリクロルホン、トリフルムロン、トリメタカルブ、
バミドチオン、バニリプロール、バーティシリウム・レカニイ(Verticillium lecanii)、
YI5302、ゼータ−シペルメトリン、ゾラプロホス、
(1R−cis)−[5−(フェニルメチル)−3−フラニル]−メチル−3−「(ジヒドロ−2−オキソ−3(2H)−フラニリデン)−メチル]−2,2−ジメチルシクロプロパンカルボキシレート、
(3−フェノキシフェニル)−メチル−2,2,3,3−テトラメチルシクロプロパンカルボキシレート、
1−[(2−クロロ−5−チアゾリル)メチル]テトラヒドロ−3,5−ジメチル−N−ニトロ−1,3,5−トリアジン−2(1H)−イミン、
2−(2−クロロ−6−フルオロフェニル)−4−[4―(1,1−ジメチルエチル)フェニル]−4,5−ジヒドロ−オキサゾール、
2−(アセチルオキシ)−3−ドデシル−1,4−ナフタレンジオン、
2−クロロ−N−[[[4−(1−フェニルエトキシ)−フェニル]−アミノ]−カルボニル]−ベンズアミド、
2−クロロ−N−[[[4−(2、2−ジクロロ−1,1−ジフルオロエトキシ)−フェニル]−アミノ]−カルボニル]−ベンズアミド、
プロピルカルバミン酸3−メチルフェニル、
4−[4−(4−エトキシフェニル)−4−メチルフェニル]―1−フルオロ−2−フェノキシ−ベンゼン、
4−クロロ−2−(1,1−ジメチルエチル)−5−[[2−(2,6−ジメチル−4−フェノキシフェノキシ)エチル]チオ]−3(2H)−ピリダジノン、
4−クロロ−2−(2−クロロ−2−メチルプロピル)−5−[(6−ヨード−3−ピリジニル)メトキシ]−3(2H)−ピリダジノン、
4−クロロ−5−[(6−クロロ−3−ピリジニル)メトキシ]−2−(3,4−ジクロロフェニル)−3(2H)−ピリダジノン、
バチルス−スリンジエンシス(Bacillus thuringiensis)EG−2348株、
[2−ベンゾイル−1−(1,1−ジメチルエチル)−ヒドラジノ安息香酸、
酪酸2,2−ジメチル−3−(2,4−ジクロロフェニル)−2−オキソ−1−オキサスピロ[4.5]デク−3−エン−4−イル
[3−[(6−クロロ−3−ピリジニル)メチル]−2−チアゾリジニリデン]−シンナミド、
ジヒドロ−2−(ニトロメチレン)−2H−1,3−チアジン−3(4H)−カルボキシアルデヒド、
[2−[[1,6−ジヒドロ−6−オキソ−1−(フェニルメチル)−4−ピリダジニル]オキシ]エチル]カルバミン酸エチル、
N−(3,4,4−トリフルオロ−1−オキソ−3−ブテニル)−グリシン、
N−(4−クロロフェニル)−3−「4−(ジフルオロメトキシ)フェニル]−4,5−ジヒドロ−4−フェニル−1H−ピラゾール−1−カルボキサミド、
N−[(2−クロロ−5−チアゾリル)メチル]−N’−メチル−N”−ニトロ−グアニジン、
N−メチル−N’−(1−メチル−2−プロペニル)−1,2−ヒドラジンジカルボチオアミド、
N−メチル−N’−2−プロペニル−1,2−ヒドラジンジカルボチオアミド、
[2−(ジプロピルアミノ)−2−オキソエチル]−エチルホスホルアミドチオ酸O,O−ジエチル、
N−シアノメチル−4−トリフルオロメチル−ニコチンアミド、
3,5−ジクロロ−1−(3,3−ジクロロ−2−プロペニルオキシ)−4−[3−(5−トリフルオロメチルピリジン−2−イルオキシ)−プロポキシ]−ベンゼン。
(実施例1)
0.29g(1.3mmol)の3’−クロロ−4’−フルオロ−1,1’−ビフェニル−2−アミンおよび0.36g(1.56mmol)の塩化2−メチル−4−(トリフルオロメチル)−1,3−チアゾール−5−カルボニルを6mLのテトラヒドロフランに溶解し、0.36mL(2.6mmol)のトリエチルアミンを添加する。その反応溶液を60℃で16時間攪拌する。処理については、その溶液を濃縮し、残留物を、シクロヘキサン/酢酸エチルを使用するシリカゲルでのクロマトグラフィーに付す。
0.185g(0.88mmol)の4−ブロモ−2−クロロ−1−フルオロベンゼン、0.243g(2.5mmol)の酢酸カリウムおよび0.21g(0.83mmol)のピナコールジボロン酸エステルを8mLのジメチルスルホキシドに懸濁させ、アルゴン下で触媒量(約5mol%)の塩化1,1’−ビス(ジフェニルホスフィノ)フェロセンパラジウム(II)を添加する。その反応溶液を80℃で2時間加熱し、その後、0.33g(0.8mmol)のN−(2−ヨードフェニル)−2−メチル−4−(トリフルオロメチル)−1,3−チアゾール−5−カルボキサミド、2.5mLの炭酸ナトリウム2M溶液およびさらなる触媒量の塩化ビス(ジフェニルホスフィノ)フェロセンパラジウム(II)を添加する。その混合物を80℃で16時間攪拌する。処理については、その反応溶液を50mLの酢酸エチルまたはジクロロメタンに吸収させ、水(5mLから10mL)で洗浄して、硫酸マグネシウムで乾燥させ、活性炭を添加して、その混合物を濾過し、濃縮する。残留物を、シクロヘキサン/酢酸エチルを使用するシリカゲルでのクロマトグラフィーに付す。
(調製例(III−1))
(調製例(IV−1))
logP(pH2.3)=2.79のN−(2−ブロモフェニル)−2−メチル−4−(トリフルオロメチル)−1,3−チアゾール−5−カルボキサミドを、実施例(IV−1)と類似に得た。
(実施例A)
スファエロセカ属(Sphaerotheca)試験(キュウリ)/保護的
溶媒:アセトン 24.5重量部
ジメチルアセトアミド 24.5重量部
乳化剤:アルキルアリールポリグリコールエーテル 1.0重量部
活性化合物の適する調製物を製造するために、1重量部の活性化合物と示した量の溶媒および乳化剤とを混合し、その濃縮物を水で所望の濃度に希釈する。
ベンチュリア属(Venturia)試験(リンゴ)/保護的
溶媒:アセトン 24.5重量部
ジメチルアセトアミド 24.5重量部
乳化剤:アルキルアリールポリグリコールエーテル 1.0重量部
活性化合物の適する調製物を製造するために、1重量部の活性化合物と示した量の溶媒および乳化剤とを混合し、その濃縮物を水で所望の濃度に希釈する。
ボトリチス属(Botrytis)試験(マメ)/保護的
溶媒:アセトン 24.5重量部
ジメチルアセトアミド 24.5重量部
乳化剤:アルキルアリールポリグリコールエーテル 1.0重量部
活性化合物の適する調製物を製造するために、1重量部の活性化合物と示した量の溶媒および乳化剤とを混合し、その濃縮物を水で所望の濃度に希釈する。
微生物におけるED50を決定するためのインビトロ試験
乳化剤PS16と混合した、試験すべき活性化合物のメタノール溶液をピペッティングして、マイクロタイタプレートのウエルに入れる。溶媒が蒸発したら、200μLのバレイショ/デキストロース培地を各ウエルに添加する。
Claims (15)
- 下記式(I):
R1およびR2は、互いに独立に、ハロゲン、シアノ、ニトロ、C1〜C6−アルキル、C2〜C6−アルケニル、C1〜C4−アルコキシ、C1〜C4−アルキルチオ、C1〜C4−アルキルスルホニル、C3〜C6−シクロアルキルを表すか、各々の場合において、ハロゲン原子を1から5個有するC1〜C4−ハロアルキル、C1〜C4−ハロアルコキシ、C1〜C4−ハロアルキルチオまたはC1〜C4−ハロアルキルスルホニルを表し、
さらに、R1およびR2は、互いにオルト配置にある場合には一緒に、場合によってはハロゲン置換またはC1〜C6−アルキル置換されているアルケニレンを表す)
のチアゾリルカルボキシアニリド。 - R1およびR2が、互いに独立に、フッ素、塩素、臭素、シアノ、ニトロ、メチル、エチル、n−またはi−プロピル、n−、i−、s−またはt−ブチル、メトキシ、エトキシ、メチルチオ、エチルチオ、n−またはi−プロピルチオ、シクロプロピル、トリフルオロメチル、トリクロロメチル、トリフルオロエチル、ジフルオロメトキシ、トリフルオロメトキシ、ジフルオロクロロメトキシ、トリフルオロエトキシ、ジフルオロメチルチオ、ジフルオロクロロメチルチオまたはトリフルオロメチルチオを表し、
さらに、R1およびR2が、互いにオルト配置にある場合には一緒に、場合によってはフッ素置換、塩素置換、臭素置換またはメチル置換されているブタジエニレンを表す、
請求項1に記載の式(I)のチアゾリルカルボキシアニリド。 - R1およびR2が、互いに独立に、フッ素、塩素、臭素、メチル、トリフルオロメチル、ジフルオロメトキシまたはトリフルオロメトキシを表す、請求項1に記載の式(I)のチアゾリルカルボキシアニリド。
- R1がフッ素を表し、R2が塩素を表す、請求項1に記載の式(I)のチアゾリルカルボキシアニリド。
- R1がフッ素を表し、R2がフッ素を表す、請求項1に記載の式(I)のチアゾリルカルボキシアニリド。
- R1がメチルまたはトリフルオロメチルを表す、請求項1に記載の式(I)のチアゾリルカルボキシアニリド。
- a)下記式(II):
のハロゲン化チアゾールカルボニルと、下記式(III):
のアニリン誘導体とを、適する場合には酸結合剤の存在下、および適する場合には希釈剤の存在下で反応させること、または
b)下記式(IV):
のハロチアゾールカルボキシアニリドと、下記式(V):
R1およびR2は、請求項1において定義されているとおりであり、
G1およびG2は、各々水素を表すか、一緒にテトラメチルエチレンを表す)
のボロン酸誘導体とを、触媒の存在下、適する場合には酸結合剤の存在下、および適する場合には希釈剤の存在下で反応させること、または
c)下記式(VI)
のチアゾールカルボキシアニリドボロン酸誘導体と、下記式(VII):
R1およびR2は、請求項1において定義されているとおりであり、および
X3は、臭素、ヨウ素またはトリフルオロメチルスルホニルオキシを表す)
のハロベンゼン誘導体とを、触媒の存在下、適する場合には酸結合剤の存在下、および適する場合には希釈剤の存在下で反応させること、
を特徴とする、請求項1に記載の式(I)のチアゾリルカルボキシアニリドの調製方法。 - 少なくとも一つの請求項1に記載の式(I)のチアゾリルカルボキシアニリドに加えて、増量剤および/または界面活性剤を含むことを特徴とする、望ましくない微生物を防除するための組成物。
- 望ましくない微生物を防除するための、請求項1に記載の式(I)のチアゾリルカルボキシアニリドの使用。
- 請求項1に記載の式(I)のチアゾリルカルボキシアニリドを微生物および/またはそれらの生息場所に塗布することを特徴とする、望ましくない微生物の防除方法。
- 請求項1に記載の式(I)のチアゾリルカルボキシアニリドを増量剤および/または界面活性剤と混合することを特徴とする、望ましくない微生物を防除するための組成物の調製方法。
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JP2011525518A (ja) * | 2008-06-25 | 2011-09-22 | ビーエーエスエフ ソシエタス・ヨーロピア | 置換ビフェニル類の製造方法 |
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- 2003-01-22 DE DE50306845T patent/DE50306845D1/de not_active Expired - Lifetime
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- 2003-01-22 PL PL371414A patent/PL215623B1/pl not_active IP Right Cessation
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Also Published As
Publication number | Publication date |
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ATE357434T1 (de) | 2007-04-15 |
PT1474406E (pt) | 2007-06-28 |
US7098227B2 (en) | 2006-08-29 |
AU2003202585A1 (en) | 2003-09-02 |
EP1474406A1 (de) | 2004-11-10 |
PL371414A1 (en) | 2005-06-13 |
EP1474406B1 (de) | 2007-03-21 |
PL215623B1 (pl) | 2014-01-31 |
JP4558325B2 (ja) | 2010-10-06 |
DE50306845D1 (de) | 2007-05-03 |
WO2003066609A1 (de) | 2003-08-14 |
DK1474406T3 (da) | 2007-07-23 |
ES2282600T3 (es) | 2007-10-16 |
DE10204390A1 (de) | 2003-08-14 |
US20050143428A1 (en) | 2005-06-30 |
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