JP5300740B2 - スピロ環式テトロン酸誘導体 - Google Patents
スピロ環式テトロン酸誘導体 Download PDFInfo
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- JP5300740B2 JP5300740B2 JP2009545139A JP2009545139A JP5300740B2 JP 5300740 B2 JP5300740 B2 JP 5300740B2 JP 2009545139 A JP2009545139 A JP 2009545139A JP 2009545139 A JP2009545139 A JP 2009545139A JP 5300740 B2 JP5300740 B2 JP 5300740B2
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/94—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom spiro-condensed with carbocyclic rings or ring systems, e.g. griseofulvins
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/56—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom 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
- C07D307/60—Two oxygen atoms, e.g. succinic anhydride
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
- C07D407/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
Description
又は
R1及びR2は、これらが結合している炭素原子と一緒に、1つ若しくは2つのヘテロ原子により場合によって分断され得る置換されていない若しくは置換された環を表し、並びに
R3は、場合によってハロゲン置換されたC1−C4−アルキルを表し、
又は
R1、R2及びR3は、これらが結合している炭素原子と一緒に、場合によって置換されたアダマンチルを表す。)
Halは、ハロゲン(特に、塩素又は臭素)を表す。)
と、
又は
Aβ)適宜希釈剤の存在下で、及び酸結合剤の存在下で、式(IV)のカルボン酸無水物
並びに、Uは、カルボニルジイミダゾール、カルボニルジイミド(例えば、ジシクロヘキシルカルボンジイミドなど)などのカルボン酸活性化試薬、リン酸化剤(例えば、POCI3、BOP−Clなど)、例えば、塩化チオニル、塩化オキサリル、ホスゲン又はクロロギ酸エステルなどのハロゲン化剤によって導入される脱離基を表す。)
と、反応させたときに得られる。
(R1及びR2がメチルを表す場合には、R3はエチル、プロピル又はメトキシを表す。)、
又は
好ましくは、R1及びR2は、これらが結合している炭素原子と一緒に、1つ若しくは2つの硫黄及び/又は酸素原子により場合によって分断され得及び置換されていない若しくはメチル若しくはエチルにより場合によって一置換若しくは二置換された五員環若しくは六員環を表し、並びに
好ましくは、R3は、フッ素若しくは塩素によって、場合によって一置換から五置換されたC1−C4−アルキルを表し、
又は
好ましくは、R1、R2及びR3は、これらが結合している炭素原子と一緒に、アダマンチルを表す。
又は
特に好ましくは、R1及びR2は、これらが結合している炭素原子と一緒に、1つ若しくは2つの酸素原子により場合によって分断され得及び置換されていない若しくはメチルにより場合によって一置換若しくは二置換された五員環若しくは六員環を表し、並びに
R3は、特に好ましくは、メチル、エチル若しくはトリフルオロメチルを表し、
又は
特に好ましくは、R1、R2及びR3は、これらが結合している炭素原子と一緒に、アダマンチルを表す。
又は
極めて特に好ましくは、R1及びR2は、これらが結合している炭素原子と一緒に、1つ若しくは2つの酸素原子により場合によって分断され得る置換されていない五員環若しくは六員環を表し、並びに
R3は、極めて特に好ましくは、メチル若しくはトリフルオロメチルを表し、
又は
極めて特に好ましくは、R1、R2及びR3は、これらが結合している炭素原子と一緒に、アダマンチルを表す。
核酸合成の阻害剤
ベナラキシル、ベナラキシル−M、ブピリメート(bupirimate)、キララキシル(chiralaxyl)、クロジラコン(clozylacon)、ジメトリモール(dimethirimol)、エトリモール(ethirimol)、フララキシル(furalaxyl)、ヒメキサゾール(hymexazol)、メタラキシル(metalaxyl)、メタラキシル−M、オフレース(ofurace)、オキサジキシル(oxadixyl)、オキソリン酸(oxolinic acid)
有糸分裂及び細胞分裂の阻害剤
ベノミル(benomyl)、カルベンダジム(carbendazim)、ジエトフェンカルブ(diethofencarb)、フベリダゾール(fuberidazol)、ペンシクロン(pencycuron)、チアベンダゾール(thiabendazol)、チオファナート−メチル(thiophanat−methyl)、ゾキサミド(zoxamid)
呼吸鎖複合体Iの阻害剤
ジフルメトリム(diflumetorim)
呼吸鎖複合体IIの阻害剤
ボスカリド(Boscalid)、カルボキシン(Carboxin)、フェンフラム(Fenfuram)、フルトラニル(Flutolanil)、フラメトピル(Furametpyr)、メプロニル(Mepronil)、オキシカルボキシン(Oxycarboxi)、ペンチオピラド(Pentbiopyrad)、チフルザミド(Thifluzamid)
呼吸鎖複合体IIIの阻害剤
アゾキシストロビン(azoxystrobin)、シアゾファミド(cyazofamid)、ジモキシストロビン(dimoxystrobin)、エネストロビン(enestrobin)、ファモキサドン(famoxadone)、フェナミドン(fenamidone)、フルオキサストロビン(fluoxastrobin)、クレソキシム−メチル(kresoxim−methyl)、メトミノストロビン(metominostrobin)、オリサストロビン(orysastrobin)、ピラクロストロビン(pyraclostrobin)、ピコキシストロビン(picoxystrobin)、トリフロキシストロビン(trifloxystrobin)
脱共役剤
ジノキャプ(dinocap)、フルアジナム(fluazinam)
ATP産生の阻害剤
酢酸フェンチン、塩化フェンチン、水酸化フェンチン、シルチオファム(silthiofam)
アミノ酸生合成及びタンパク質生合成の阻害剤
アンドプリム(andoprim)、ブラスチシジン−S(blasticidin−S)、シプロジニル(cyprodinil)、カスガマイシン(kasugamycin)、カスガマイシン塩酸塩水和物、メパニピリム(mepanipyrim)、ピリメタニル(pyrimethanil)
シグナル伝達の阻害剤
フェンピクロニル(fenpiclonil)、フルジオキソニル(fludioxonil)、キノキシフェン(quinoxyfen)
脂質及び膜合成の阻害剤
クロゾリナート(chlozolinate)、イプロジオン(iprodione)、プロシミドン(procymidone)、ビンクロゾリン(vinclozolin)
アムプロピルフォス(ampropylfos)、カリウム−アムプロピルフォス、エジフェンホス(edifenphos)、イプロベンホス(iprobenfos(IBP))、イソプロチオラン(isoprothiolan)、ピラザホス(pyrazophos)
トルクロホス−メチル(tolclofos−methyl)、ビフェニル
ヨードカルブ(iodocarb)、プロパモカルブ(propamocarb)、プロパモカルブ塩酸塩(propamocarb hydrochloride)
エルゴステロール生合成の阻害剤
フェンキサミド、
アザコナゾール(azaconazol)、ビテルタノール(bitertanol)、ブロムコナゾール(bromuconazole)、シプロコナゾール(cyproconazole)、ジクロブトラゾール(diclobutrazole)、ジフェノコナゾール(difenoconazole)、ジニコナゾール(diniconazole)、ジニコナゾール−M(diniconazole−M)、エポキシコナゾール(epoxiconazole)、エタコナゾール(etaconazole)、フェンブコナゾール(fenbuconazole)、フルキンコナゾール(fluquinconazole)、フルシラゾール(flusilazole)、フルトリアフォール(flutriafol)、フルコナゾール(furconazole)、フルコナゾール−シス(furconazole−cis)、ヘキサコナゾール(hexaconazole)、イミベンコナゾール(imibenconazole)、イプコナゾール(ipconazole)、メトコナゾール(metconazole)、ミクロブタニル(myclobutanil)、パクロブトラゾール(paclobutrazole)、ペンコナゾール(penconazole)、プロピコナゾール(propiconazole)、プロチオコナゾール(prothioconazole)、シメコナゾール(simeconazole)、テブコナゾール(tebuconazole)、テトラコナゾール(tetraconazole)、トリアジメフォン(triadimefon)、トリアジメノール(triadimenol)、トリチコナゾール(triticonazole)、ユニコナゾール(uniconazole)、ボリコナゾール(voriconazole)、イマザリル(imazalil)、イマザリルサルファート(imazalil sulphate)、オキスポコナゾール(oxpoconazol)、フェナリモール(fenarimol)、フルルプリミドール(flurprimidol)、ヌアリモール(nuarimol)、ピリフェノックス(pyrifenox)、トリフォリン(triforin)、ペフラゾアート(pefurazoate)、プロクロラズ(prochloraz)、トリフルミゾール(triflumizol)、ビニコナゾール(viniconazole)
アルジモルフ(aldimorph)、ドデモルフ(dodemorph)、ドデモルフ・アセタート(dodemorph acetate)、フェンプロピモルフ(fenpropimorph)、トリデモルフ(tridemorph)、フェンプロピジン(fenpropidin)、スピロキサミン(spiroxamine)、
ナフチフィン(naftifine)、ピリブチカルブ(pyributicarb)、テルビナフィン(terbinafine)
細胞壁合成の阻害剤
ベンチアバリカルブ(benthiavalicarb)、ビアラホス(bialaphos)、ジメトモルフ(dimethomorph)、フルモルフ(flumorph)、イプロバリカルブ(iprovalicarb)、ポリオキシン(polyoxin)、ポリオキソリム(polyoxorim)、バリダマイシンA(validamycin A)
メラニン生合成の阻害剤
カプロパミド(capropamid)、ジクロシメト(diclocymet)、フェノキサニル(fenoxanil)、フタリド(phtalide)、ピロキロン(pyroquilon)、トリシクラゾール(tricyclazole)
耐性誘導剤
アシベンゾラール−S−メチル(acibenzolar−S−methyl)、プロベナゾール(probenazol)、チアジニル(tiadinil)
複数部位
カプタフォール(captafol)、カプタン(captan)、クロロサロニル(chlorothalonil)、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−銅及びボルドー混合物(Bordeaux mixture)などの銅塩、ジクロフルアニド(dichlofluanid)、ジチアノン(dithianon)、ドジン(dodine)、ドジン遊離塩基(dodine free base)、フェルバム(ferbam)、フォルペット(folpet)、フルオロフォルペット(fluorofolpet)、グアザチン(guazatine)、グアザチンアセタート(guazatin acetate)、イミノクタジン(iminoctadin)、イミノクタジン・アルベシラート(iminoctadine albesilate)、イミノクタジン・トリアセタート(iminoctadine triacetate)、マンコッパー(mancopper)、マンコゼブ(mancozeb)、マネブ(maneb)、メチラム(metiram)、メチラム亜鉛(metiram zinc)、プロピネブ(propineb)、硫黄及びカルシウム多硫化物を含む硫黄調製物)、チラム(thiram)、トリルフルアニド(tolylfluanid)、ジネブ(zineb)、ジラム(ziram)
未知の機序
アミブロムドール(amibromdol)、ベンチアゾール(benthiazole)、ベトキサジン(bethoxazin)、キャプシマイシン(capsimycin)、カルボン(carvon)、チノメチオナート(chinomethionat)、クロロピクリン(chloropicrin)、キュフラネブ(cufraneb)、シフルフェナミド(cyflufenamide)、シモキサニル(cymoxanil)、ダゾメット(dazomet)、デバカルブ(debacarb)、ジクロメジン(diclomezin)、ジクロロフェン(dichlorophen)、ジクロラン(dicloran)、ジフェンゾクアート(difenzoquat)、ジフェンゾクアート・メチルサルファート(difenzoquat methyl sulphate)、ジフェニルアミン(diphenylamine)、エタボキサム(ethaboxam)、フェリムゾン(ferimzone)、フルメトバール(flumetover)、フルスルファミド(flusulfamide)、フルオピコリド(fluopicolide)、フルオロイミド(fluoroimide)、ヘキサクロロベンゼン(hexachlorobenzene)、8−ヒドロキシキノリンサルファート(8−hydroxychinolinsulfate)、イルママイシン(irumamycin)、メタサルフォカルブ(methasulphocarb)、メトラフェノン(metrafenone)、メチルイソチオシアナート(methyl isothiocyanate)、ミルジオマイシン(mildiomycin)、ナタマイシン(natamycin)、ニッケルジメチルジチオカルバマート(nickel dimethyldithiocarbamate)、ニトロサール−イソプロピル(nitrothal−isopropyl)、オクチリノン(octhilinone)、オキサモカルブ(oxamocarb)、オキシフェンチイン(oxyfenthiin)、ペンタクロロフェノール(pentachlorophenol)及び塩、2−フェニルフェノール(2−phenylphenol)及び塩、ピペラリン(piperalin)、プロパノシン−ナトリウム(propanosin−sodium)、プロキナジド(proquinazid)、ピロルニトリン(pyrrolnitrin)、キントゼン(quintozen)、テクロフタラム(tecloftalam)、テクナゼン(tecnazen)、トリアゾキシド(triazoxid)、トリクラミド(trichlamid)、ザリラミド(zarilamid)及び2,3,5,6−テトラクロロ−4−(メチルスルホニル)ピリジン、N−(4−クロロ−2−ニトロフェニル)−N−エチル−4−メチルベンゼンスルホンアミド、2−アミノ−4−メチル−N−フェニル−5−チアゾールカルボキサミド、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、3−[5−(4−クロロフェニル)−2,3−ジメチルイソオキサゾリジン−3−イル]ピリジン、シス−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、2,4−ジヒドロ−5−メトキシ−2−メチル−4−[[[[1−[3−(トリフルオロメチル)フェニル]エチリデン]アミノ]オキシ]メチル]フェニル]−3H−1,2,3−トリアゾール−3−オン(185336−79−2)、メチル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−カルボキシラート、3,4,5−トリクロロ−2,6−ピリジンジカルボニトリル、メチル2−[[[シクロプロピル[(4−メトキシフェニル)イミノ]メチル]チオ]メチル]フェニル−α−(メトキシメチレン)ベンゾアセタート、4−クロロ−α−プロピニルオキシ−N−[2−[3−メトキシ−4−(2−プロピニルオキシ)フェニル]エチル]ベンゾアセトアミド、(2S)−N−[2−[4−[[3−(4−クロロフェニル)−2−プロピニル]オキシ]−3−メトキシフェニル]エチル]−3−メチル−2−[(メチルスルホニル)アミノ]ブタンアミド、5−クロロ−7−(4−メチルピペリジン−1−イル)−6−(2,4,6−トリフルオロフェニル)[1,2,4]トリアゾロ[1,5−a]ピリミジン、5−クロロ−6−(2,4,6−トリフルオロフェニル)−N−[(1R)−1,2,2−トリメチルプロピル]−[1,2,4]トリアゾロ[1,5−a]ピリミジン−7−アミン、5−クロロ−N−[(1R)−1,2−ジメチルプロピル]−6−(2,4,6−トリフルオロフェニル)[1,2,4]トリアゾロ[1,5−a]ピリジミン−7−アミン、N−[1−(5−ブロモ−3−クロロピリジン−2−イル)エチル]−2,4−ジクロロニコチンアミド、N−(5−ブロモ−3−クロロピリジン−2−イル)メチル−2,4−ジクロロニコチンアミド、2−ブトキシ−6−ヨード−3−プロピルベンゾピラノン−4−オン、N−{(Z)−[(シクロプロピルメトキシ)イミノ][6−(ジフルオロメトキシ)−2,3−ジフルオロフェニル]メチル}−2−ベンゾアセトアミド、N−(3−エチル−3,5,5−トリメチルシクロヘキシル)−3−ホルミルアミノ−2−ヒドロキシベンズアミド、2−[[[[1−[3(1−フルオロ−2−フェニルエチル)オキシ]フェニル]エチリデン]アミノ]オキシ]メチル]−α−(メトキシイミノ)−N−メチル−α−ベンゾアセトアミド、N−{2−[3−クロロ−5−(トリフルオロメチル)ピリジン−2−イル]エチル}−2−(トリフルオロメチル)ベンズアミド、N-(3’,4’−ジクロロ−5−フルオロビフェニル−2−イル−3−(ジフルオロメチル)−1−メチル−1H−ピラゾール−4−カルボキサミド、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、1−[(4−メトキシフェノキシ)メチル]−2,2−ジメチルプロピル−1H−イミダゾール1−カルボン酸、O−[1−[(4−メトキシフェノキシ)メチル]−2,2−ジメチルプロピル]−1H−イミダゾ1−1−カルボチオ酸、2−(2−{[6−(3−クロロ−2−メチルフェノキシ)−5−フルオロピリミジン−4−イル]オキシ}フェニル)−2−(メトキシイミノ)−N−メチル−アセトアミド。
ブロノポール(bronopol)、ジクロロフェン(dichlorophen)、ニトラピリン(nitrapyrin)、ニッケル−ジメチルジチオカルバマート(nickel−dimethyldithiocarbamate)、カスガマイシン(kasugamycin)、オクチリノン(octhilinon)、フランカルボン酸(furancarboxylic acid)、オキシテトラサイクリン(oxytetracyclin)、プロベナゾール(probenazol)、ストレプトマイシン(streptomycin)、テクロフタラム(tecloftalam)、硫酸銅及びその他の銅調製物。
アセチルコリンエステラーゼ(AChE)阻害剤
カルバマート、
例えば、アラニカルブ(alanycarb)、アルジカルブ(aldicarb)、アルドキシカルブ(aldoxycarb)、アリキシカルブ(allyxycarb)、アミノカルブ(aminocarb)、ベンジオカルブ(bendiocarb)、ベンフラカルブ(benfuracarb)、ブフェンカルブ(bufencarb)、ブタカルブ(butacarb)、ブトカルボキシム(butocarboxim)、ブトキシカルボキシム(butoxycarboxim)、カルバリル(carbaryl)、カルボフラン(carbofuran)、カルボサルファン(carbosulphan)、クロエトカルブ(chloethocarb)、ジメチラン(dimetilan)、エチオフェンカルブ(ethiofencarb)、フェノブカルブ(fenobucarb)、フェノチオカルブ(fenothiocarb)、フォルメタナート(formetanate)、フラチオカルブ(furathiocarb)、イソプロカルブ(isocarb)、メタム−ナトリウム(metam−sodium)、メチオカルブ(methiocarb)、メトミル(methomyl)、メトルカルブ(metolcarb)、オキサミル(oxamyl)、ピリミカルブ(pirimicarb)、プロメカルブ(promecarb)、プロポクスール(propoxur)、チオジカルブ(thiodicarb)、チオファノックス(thiofanox)、トリメタカルブ(trimethacarb)、XMC、キシリルカルブ(xylylcarb)、トリアザマート
有機リン酸塩、
例えば、アセファート(acephate)、アザメチフォス(azamethiphos)、アジンフォス(azinphos)(−メチル、−エチル)、ブロモフォス−エチル(bromophos−ethyl)、ブロムフェンビンフォス(bromfenvinfos)(−メチル)、ブタチオフォス(butathiofos)、カヅサフォス(cadusafos)、カルボフェノチオン(carbophenothion)、クロレトキシフォス(chlorethoxyfos)、クロルフェンビンフォス(chlorfenvinphos)、クロルメフォス(chlormephos)、クロルピリフォス(chlorpyrifos)(−メチル/−エチル)、クマフォス(coumaphos)、シアノフェンフォス(cyanofenphos)、シアノフォス(cyanophos)、クロロフェンビンフォス(chlorofenvinphos)、デメトン(demeton)−S−メチル、デメトン(demeton)−S−メチルスルフォン、ダイアライフォス(dialifos)、ダイアジノン(diazinon)、ジクロフェンチオン(dichlofenthion)、ジクロルボス(dichlorvos)/DDVP、ジクロトフォス(dicrotophos)、ジメトアート(dimethoate)、ジメチルビンフォス(dimethylvinphos)、ジオキサベンゾフォス(dioxabenzofos)、ジスルフォトン(disulfoton)、EPN、エチオン(ethion)、エトプロフォス(ethoprophos)、エトリンフォス(etrimfos)、ファムフール(famphur)、フェナミフォス(fenamiphos)、フェニトロチオン(fenitrothion)、フェンスルフォチオン(fensulfothion)、フェンチオン(fenthion)、フルピラゾフォス(flupyrazofos)、フォノフォス(fonofos)、フォルモチオン(formothion)、フォスメチラン(fosmethilan)、フォスチアザート(fosthiazate)、ヘプテノフォス(heptenophos)、ヨードフェンフォス(iodofenphos)、イプロベンフォス(iprobenfos)、イサゾフォス(isazofos)、イソフェンフォス(isofenphos)、o−サリチル酸イソプロピル(isopropyl o−salicylate)、イソキサチオン(isoxathion)、マラチオン(malathion)、メカルバム(mecarbam)、メタクリフォス(methacrifos)、メタミドフォス(methamidophos)、メチダチオン(methidathion)、メビンフォス(mevinphos)、モノクロトフォス(monocrotophos)、ネイルド(naled)、オメトエート(omethoate)、オキシデメトン(oxydemeton)−メチル、パラチオン(parathion)(−メチル/−エチル)、フェントエート(phenthoate)、フォラート(phorate)、フォサロン(phosalone)、フォスメト(phosmet)、フォスファミドン(phosphamidon)、フォスフォカルブ(phosphocarb)、フォキシム(phoxim)、ピリミフォス(pirimiphos)(−メチル/−エチル)、プロフェノフォス(profenofos)、プロパフォス(propaphos)、プロペタンフォス(propetamphos)、プロチオフォス(prothiofos)、プロトエート(prothoate)、ピラクロフォス(pyraclofos)、ピリダフェンチオン(pyridaphenthion)、ピリダチオン(pyridathion)、キナルフォス(quinalphos)、セブフォス(sebufos)、スルフォテプ(sulfotep)、スルプロフォス(sulprofos)、テブピリンフォス(tebupirimfos)、テメフォス(temephos)、テルブフォス(terbufos)、テトラクロロビンフォス(tetrachlorovinphos)、チオメトン(thiometon)、トリアゾフォス(triazophos)、トリクロルフォン(triclorfon)、バミドチオン(vamidothion)
ナトリウムチャンネル調節物質/電圧依存性ナトリウムチャンネル遮断剤
ピレトロイド(pyrethroid)
例えば、アクリナトリン(acrinathrin)、アレトリン(allethrin)(d−シス−トランス、d−トランス)、β−サイフルトリン(cyfluthrin)、ビフェントリン(bifenthrin)、ビオアレトリン(bioallethrin)、ビオアレトリン(bioallethrin)−S−シクロペンチル(cyclopentyl)異性体、ビオエタノメトリン(bioethanomethrin)、ビオペルメトリン(biopermethrin)、ビオレスメトリン(bioresmethrin)、クロバポルトリン(chlovaporthrin)、シス−サイペルメトリン(cys−cypermethrin)、シス−レスメトリン(cis−resmethrin)、シス−ペルメトリン(cis−permethrin)、クロサイトリン(clocythrin)、シクロプロトリン(cycloprothrin)、サイフルトリン(cyfluthrin)、サイハロトリン(cyhalothrin)、サイペルメトリン(cypermethrin)(α−、β−、θ−、ζ−)、サイフェノトリン(cyphenothrin)、デルタメトリン(deltamethrin)、エムペントリン(empenthrin)(1R−異性体)、エスフェンバレラート(esfenvalerate)、エトフェンプロクス(etofenprox)、フェンフルトリン(fenfluthrin)、フェンプロパトリン(fenpropathrin)、フェンピリトリン(fenpyrithrin)、フェンバレラート(fenvalerate)、フルブロサイトリナート(flubrocythrinate)、フルサイトリナート(flucythrinate)、フルフェンプロクス(flufenprox)、フルメトリン(flumethrin)、フルバリナート(fluvalinate)、フブフェンプロクス(fubfenprox)、γ−サイハロトリン(gamma−cyhalothrin)、イミプロトリン(imiprothrin)、カデトリン(kadethrin)、λ−サイハロトリン(lambda−cyhalothrin)、メトフルトリン(metofluthrin)、ペルメトリン(permethrin)(シス−、トランス−)、フェノトリン(phenothrin)(1R−トランス異性体)、プラレトリン(prallethrin)、プロフルトリン(profluthrin)、プロトリフェンビュート(protrifenbute)、ピレスメトリン(pyresmethrin)、レスメトリン(resmethrin)、RU15525、シラフルオフェン(silafluofen)、τ−フルバリナート(tau−fluvalinate)、テフルトリン(tefluthrin)、テラレトリン(terallethrin)、テトラメトリン(tetramethrin)(1R−異性体)、トラロメトリン(tralomethrin)、トランスフルトリン(transfluthrin)、ZXI8901、ピレトリン(pyrethrin)(ピレトラム(pyrethrum)
DDT
オキサジアジン
例えば、インドキサカルブ(indoxacarb)
セミカルバゾン、
例えば、メタフルミゾン(BAS3201)
アセチルコリン受容体アゴニスト/アンタゴニスト
クロロニコチニル、
例えば、アセトアミプリド(acetamiprid)、クロチアニジン(clothianidin)、ジノテフラン(dinotefuran)、イミダクロプリド(imidacloprid)、ニテンピラム(nitenpyram)、ニチアジン(nithiazine)、チアクロプリド(thiacloprid)、チアメトキサム(thiamethoxam)
ニコチン、ベンサルタップ(bensultap)、カルタップ(cartap)
アセチルコリン受容体調節物質
スピノシン、
例えば、スピノサド(spinosad)
GABA調節型塩化物チャンネルアンタゴニスト
有機塩素、
例えば、カムフェクロール(camphechlor)、クロロダン(chlorodane)、エンドスルファン(endosulfan)、γ−HCH、HCH、ヘプタクロル(heptachlor)、リンデイン(lindane)、メトキシクロル(methoxychlor)
フィプロール(fiprol)、
例えば、アセトプロール(acetoprole)、エチプロール(ethiprole)、フィプロニル(fipronil)、ピラフルプロール(pyrafluprole)、ピリプロール(pyriprole)、バニリプロール(vaniliprole)
塩化物チャンネル活性化因子
メクチン(mectin)、
例えば、アバルメクチン(abarmectin)、エマメクチン(emamectin)、エマメクチン−ベンゾアート(emamectin−benzoate)、イベルメクチン(ivermectin)、レピメクチン(lepimectin)、ミルベマイシン(milbemycin)
幼若ホルモン類似体、
例えば、ジオフェノラン(diofenolan)、エポフェノナン(epofenonane)、フェノキシカルブ(fenoxycarb)、ハイドロプレン(hydroprene)、キノプレン(kinoprene)、メトプレン(methoprene)、ピリプロキシフェン(pyriproxifen)、トリプレン(triprene)
エクジソンアゴニスト/撹乱物質
ジアシルヒドラジン(diacylhydrazine)、
例えば、クロマフェノジド(chromafenozide)、ハロフェノジド(halofenozide)、メトキシフェノジド(methoxyfenozide)、テブフェノジド(tebufenozide)
キチン生合成阻害剤
ベンゾイル尿素(benzoilurea)、
例えば、ビストリフルロン(bistrifluron)、クロフルアズロン(chlofluazuron)、ジフルベンズロン(diflubenzuron)、フルアズロン(fluazuron)、フルサイクロクスロン(flucycloxuron)、フルフェノクスロン(flufenoxuron)、ヘキサフルムロン(hexaflumuron)、ルフェヌロン(lufenuron)、ノバルロン(novaluron)、ノビフルムロン(noviflumuron)、ペンフルロン(penfluron)、テフルベンズロン(teflubenzuron)、トリフルムロン(triflumuron))
ブプロフェジン(buprofezin)
シロマジン(cyromazine)
酸化的リン酸化の阻害剤、ATP撹乱剤
ジアフェンチウロン(diafenthiuron)
有機スズ(organotin)化合物
例えば、アゾサイクロチン(azocyclotin)、サイヘキサチン(cyhexatin)、酸化フェンブタチン(fenbutatin−oxide)
Hプロトン勾配を崩壊させることによって作用する酸化的リン酸化の脱共役剤
ピロール、
例えばクロルフェナピル(chlorfenapyr)
ジニトロフェノール(dinitrophenol)、
例えば、ビナパクリル(binapacryl)、ジノブトン(dinobuton)、ジノキャプ(dinocap)、DNOC、メプチルジノキャップ
部位I電子輸送阻害剤
METI、
例えば、フェナザキン(fenazaquin)、フェンピロキシメート(fenpyroximate)、ピリミジフェン(pyrimidifen)、ピリダベン(pyridaben)、テブフェンピラド(tebufenpyrad)、トルフェンピラド(tolfenpyrad)
ヒドラメチルノン(hydramethylnon)、
ジコフォール(dicofol)
部位II電子輸送阻害剤
ロテノン
部位III電子輸送阻害剤
アセキノシル(acequinocyl)、フルアクリピリム(fluacrypyrim)
昆虫の腸膜の微生物撹乱物質;
バチルス・チューリンゲンシス(bacillus thuringiensis)株
脂質合成阻害剤
テトロン酸、
例えば、スピロジクロフェン(spirodiclofen)、スピロメシフェン(spiromesifen)
テトラミン酸、
例えば、スピロテトラマート(Spirotetramat)、シス−3−(2,5−ジメチルフェニル)−4−ヒドロキシ−8−メトキシ−1−アザスピロ[4.5]デク−3−エン−2−オン
カルボキサミド、
例えば、フロニカミド(flonicamid)
オクトパミン作動性アゴニスト
例えば、アミトラズ(amitraz)
マグネシウムによって刺激されるATPアーゼの阻害剤;
プロパルギット
ネライストキシン(nereistoxin)類縁体、
例えば、チオシクラム水素オキシラート(thiocyclam hydrogen oxalate)、チオサルタップナトリウム(thiosultap−sodium))
リアノジン受容体のアゴニスト、
ベンゾジカルボキサミド、
例えば、フルベンジアミド(flubendiamid)
アンスロニラミド(anthronilamide)
例えば、リナキシピル(rynaxypyr)(3−ブロモ−N−{4−クロロ−2−メチル−6−[(メチルアミノ)カルボニル]フェニル}−1−(3−クロロピリジン−2−イル)−1H−ピラゾール−5−カルボキサミド)
生物製剤、ホルモン又はフェロモン
アザジラクチン(azadirachtin)、バチルス種、ビューベリア(Beauveria)種、コドルモン(codlemone)、メタリジウム(Metarrhizium)種、ペシロマイセス(Paecilomyces)種、チューリンゲンシン(thuringiensin)、ベルチシリウム(Verticillium)種)
不明な作用機序又は特定されない作用機序を有する活性化合物
燻蒸剤、
例えば、リン化アルミニウム(aluminum phosphide)、臭化メチル、フッ化スルフリル
摂食阻害剤、
例えば、氷晶石(cryolite)、フロニカミド(flonicamid)、ピメトロジン(pymetrozine)
ダニ増殖阻害剤、
例えば、クロフェンテジン(clofentezine)、エトキサゾール(etoxazole)、ヘキシチアゾクス(hexythiazox)
アミドフルメト(amidoflumet)、ベンクロチアズ(benclothiaz)、ベンゾキシマート(benzoximate)、ビフェナザート(bifenazate)、ブロモプロピラート(bromopropylate)、ブプロフェジン(buprofezin)、キノメチオナート(chinomethionat)、クロルジメフォルム(chlordimeform)、クロロベンジラート(chlorobenzilate)、クロロピクリン(chloropicrin)、クロチアゾベン(clothiazoben)、シクロプレン(cycloprene)、サイフルメトフェン(cyflumetofen)、ジシクラニル(dicyclanil)、フェノキサクリム(fenoxacrim)、フェントリファニル(fentrifanil)、フルベンジミン(flubenzimine)、フルフェネリム(flufenerim)、フルテンジン(flutenzin)、ワタキバガ幼虫分泌性性誘引物質(gossyplure)、ヒドラメチルノン(hydramethylnone)、ジャポニルレ(japonilure)、メトキサジアゾン(metoxadiazone)、石油、ピペロニルブトキシド(piperonyl butoxide)、オレイン酸カリウム、ピリダリル(pyridalyl)、スルフルラミド(sulfluramid)、テトラジフォン(tetradifon)、テトラサル(tetrasul)、トリアラテン(triarathene)、ベルブチン(verbutin)。
ハジラミ(Mallophagida)目並びにマルツノハジラミ(Amblycerina)亜目及びホソツノハジラミ(Ischnocerina)亜目からは、例えば、トリメノポン属種(Trimenopon spp.)、メノポン属種(Menopon spp.)、トリノトン属種(Trinoton spp.)、ボビコラ属種(Bovicola spp.)、ウェルネッキエラ属種(Werneckiella spp.)、レピケントロン属種(Lepikentron spp.)、ダマリナ属種(Damalina spp.)、トリコデクテス属種(Trichodectes spp.)、フェリコラ属種(Felicola spp.)、
双翅目(Diptera)、及び並びにネマトセリナ亜目(Nematocerina)及びブラキセリナ亜目(Brachycerina)からは、例えば、イーデス属種(Aedes spp.)、アノフレス属種(Anopheles spp.)、キュレックス属種(Culex spp.)、シムリウム属種(Simulium spp.)、ユーシムリウム属種(Eusimulium spp.)、フレボトムス属種(Phlebotomus spp.)、ルツゾミヤ属種(Lutzomyia spp.)、キュリコイデス属種(Culicoides spp.)、クリソップス属種(Chrysops spp.)、ヒボミトラ属種(Hybomitra spp.)、アチロータス属種(Atylotus spp.)、タバヌス属種(Tabanus spp.)、ヘマトポタ属種(Haematopota spp.)、フィリポミア属種(Philipomyia spp.)、ブラウラ属種(Braula spp.)、ムスカ属種(Musca spp.)、ヒドロタエア属種(Hydrotaea spp.)、ストモキシス属種(Stomoxys spp.)、ヘマトビア属種(Haematobia spp.)、モレリア属種(Morellia spp.)、ファニア属種(Fannia spp.)、グロッシナ属種(Glossina spp.)、カリホラ属種(Calliphora spp.)、ルチリア属種(Lucilia spp.)、クリソミア属種(Chrysomyia spp.)、ウォールファルチア属種(Wohlfahrtia spp.)、サルコフォガ属種(Sarcophaga spp.)、エストラス属種(Oestrus spp.)、ヒポデルマ属種(Hypoderma spp.)、ガステロフィラス属種(Gasterophilus spp.)、ヒッポボスカ属種(Hippobosca spp.)、リポプテナ属種(Lipoptena spp.)、メロファガス属種(Melophagus spp.)、
ノミ目(Siphonapterida)からは、例えば、ピューレクス属種(Pulex spp.)、クテノセファリデス属種(Ctenocephalides spp.)、ゼノプシラ属種(Xenopsylla spp.)、セラトフィラス属種(Ceratophyllus spp.)、
カメムシ目(Heteropterida)からは、例えば、シメックス属種(Cimex spp.)、トリアトマ属種(Triatoma spp.)、ロードニウス属種(Rhodnius spp.)、パンストロンギラス属種(Panstrongylus spp.)、
ゴキブリ目(Blattarida)からは、例えば、ブラタ・オリエンタリス(Blatta orientalis)、ペリプラネタ・アメリカーナ(Periplaneta americana)、ブラテラ・ゲルマニカ(Blattella germanica)、スペラ種(Supella spp.)
アカリ亜綱(Acari)(Acarina)並びにメタスチグマタ目(Metastigmata及びメソスチグマタ目(Mesostigmata)からは、例えば、アルガス属種(Argas spp.)、オーニソドラス属種(Ornithodorus spp.)、オトビウス属種(Otobius spp.)、イキソデス属種(Ixodes spp.)、アンブリオンマ属種(Amblyomma spp.)、ブーフィラス属種(Boophilus spp.)、デルマセントール属種(Dermacentor spp.)、ヘモフィサリス属種(Haemophysalis spp.)、ヒアロンマ属種(Hyalomma spp.)、リピセファラス属種(Rhipicephalus spp.)、デルマニサス属種(Dermanyssus spp.)、ライリエチア属種(Raillietia spp.)、ニューモニサス属種(Pneumonyssus spp.)、ステルノストーマ属種(Sternostoma spp.)、バロア属種(Varroa spp.)、
ケダニ目(Actinedida)(プロスチグマタ(Prostigmata))及びコナダニ目(Acaridida)(アスチグマタ(Astigmata))からは、例えば、アカラピス属種(Acarapis spp.)、ケイレチエラ属種(Cheyletiella spp.)、オルニソケイレチア属種(Ornithocheyletia spp.)、ミオビア属種(Myobia spp.)、プソレルゲーツ属種(Psorergates spp.)、デモデックス属種(Demodex spp.)、トロンビキュラ属種(Trombicula spp.)、リストロホラス属種(Listrophorus spp.)、アカラス属種(Acarus spp.)、チロファガス属種(Tyrophagus spp.)、カログリファス属種(Caloglyphus spp.)、ヒポデクテス属種(Hypodectes spp.)、プテロリカス属種(Pterolichus spp.)、プソロプテス属種(Psoroptes spp.)、コリオプテス属種(Chorioptes spp.)、オトデクテス属種(Otodectes spp.)、サルコプテス属種(Sarcoptes spp.)、ノトエドレス属種(Notoedres spp.)、クネミドコプテス属種(Knemidocoptes spp.)、シトジテス属種(Cytodites spp.)、ラミノシオプテス属種(Laminosioptes spp.)。
膜翅類、例えば、シレックス・ジュベンカス(Sirex juvencus)、ウロセルス・ギガス(Urocerus gigas)、ウロセルス・ギガス・タイグヌス(Urocerus gigas taignus)、ウロセルス・オウガー(Urocerus augur)、
シロアリ類、例えば、カロテルメス・フラビコリス(Kalotermes flavicollis)、クリプトテルメス・ブレビス(Cryptotermes brevis)、ヘテロテルメス・インディコラ(Heterotermes indicola)、レチクリテルメス・フラビペス(Reticulitermes flavipes)、レチクリテルメス・サントネンシス(Reticulitermes santonensis)、レチクリテルメス・ルチフガス(Reticulitermes lucifugus)、マストテルメス・ダルウィニエンシス(Mastotermes darwiniensis)、ズーテルモプシス・ネバデンシス(Zootermopsis nevadensis)、コプトテルメス・フォルモサヌス(Coptotermes formosanus)、
シミ類、例えば、レピスマ・サッカリナ(Lepisma saccharina)。
ダニ目(Acarina)からは、例えば、アルガス・ペルシカス(Argas persicus)、アルガス・リフレクサス(Argas reflexus)、ブリオビア属種(Bryobia spp.)、デルマニサス・ガリナエ(Dermanyssus gallinae)、グリシファガス・ドメスティカス(Glyciphagus domesticus)、オルニトドラス・モウバット(Ornithodorus moubat)、ライピセファラス・サングイネウス(Rhipicephalus sanguineus)、トロンビキュラ・アルフレドヅゲシ(Trombicula alfreddugesi)、ニュートロンビキュラ・オウツムナリス(Neutrombicula autumnalis)、デルマトファゴイデス・プテロニシムス(Dermatophagoides pteronissimus)、デルマトファゴイデス・フォリナエ(Dermatophagoides forinae)、
クモ目(Aranaeae)からは、例えば、アビキュラリイダエ(Aviculariidae)、アラネイダエ(Araneidae)、
ザトウムシ目(Opiliones)からは、例えば、シュードスコルピオネス・チェリファー(Pseudoscorpiones chelifer)、シュードスコルピオネス・チェイリジウム(Pseudoscorpiones cheiridium)、オピリオネス・ファランジウム(Opiliones phalangium)、
ワラジムシ目(Isopoda)からは、例えば、オニスカス・アセルス(Oniscus asellus)、ポルセリオ・スカバー(Porcellio scaber)、
ヤスデ目(Diplopoda)からは、例えば、ブラニルス・グツラツス(Blaniulus guttulatus)、ポリデスムス属種(Polydesmus spp.)、
ムカデ目(Chilopoda)からは、例えば、ゲオフィルス属種(Geophilus spp.)、
シミ目(Zygentoma)からは、例えば、クテノレピスマ属種(Ctenolepisma spp.)、レピスマ・サッカリナ(Lepisma saccharina)、レピスモデス・インクイリヌス(Lepismodes inquilinus)、
ゴキブリ目(Blattaria)からは、例えば、ブラタ・オリエンタリス(Blatta orientalis)、ブラテラ・ゲルマニカ(Blattella germanica)、ブラテラ・アサヒナイ(Blattella asahinai)、ロイコファエア・マデラエ(Leucophaea maderae)、パンクロラ属種(Panchlora spp.)、パルコブラッタ属種(Parcoblatta spp.)、ペリプラネタ・オーストララシアエ(Periplaneta australasiae)、ペリプラネタ・アメリカーナ(Periplaneta americana)、ペリプラネタ・ブルネア(Periplaneta brunnea)、ペリプラネタ・フリギノサ(Periplaneta fuliginosa)、スペラ・ロンギパルパ(Supella longipalpa)、
直翅目(Saltatoria)からは、例えば、アキータ・ドメスティカス(Acheta domesticus)、
ハサミムシ目(Dermaptera)からは、フォルフィキュラ・オーリキュラリア(Forficula auricularia)、
シロアリ目(Isoptera)からは、例えば、カロテルメス属種(Kalotermes spp.)、レチキュリテルメス属種(Reticulitermes spp.)、
チャタテムシ目(Psocoptera)からは、例えば、レピナツス属種(Lepinatus spp.)、リポセリス属種(Liposcelis spp.)、
コウチュウ目(Coleoptera)からは、例えば、アンスレヌス属種(Anthrenus spp.)、アタゲヌス属種(Attagenus spp.)、デルメステス属種(Dermestes spp.)、ラテチカス・オリザエ(Latheticus oryzae)、ネクロビア属種(Necrobia spp.)、プチヌス属種(Ptinus spp.)、ライゾペルサ・ドミニカ(Rhizopertha dominica)、シトフィラス・グラナリウス(Sitophilus granarius)、シトフィラス・オリザエ(Sitophilus oryzae)、シトフィラス・ジーマイス(Sitophilus zeamais)、ステゴビウム・パニセウム(Stegobium paniceum)、
ハエ目(Diptera)からは、例えば、イーデス・アエギプチ(Aedes aegypti)、イーデス・アルビオピクタス(Aedes albopictus)、イーデス・タエニオリンクス(Aedes taeniorhynchus)、アノフェレス属種(Anopheles spp.)、カリフォラ・エリスロセファラ(Calliphora erythrocephala)、クリソゾナ・プルビアリス(Chrysozona pluvialis)、キュレックス・クインクファスシアタス(Culex quinquefasciatus)、キュレックス・ピピエンズ(Culex pipiens)、キュレックス・タルサリス(Culex tarsalis)、ドロソフィラ属種(Drosophila spp.)、ファンニア・カニキュラリス(Fannia canicularis)、ムスカ・ドメスチカ(Musca domestica)、フレボトムス属種(Phlebotomus spp.)、サルコファガ・カルナリア(Sarcophaga carnaria)、シムリウム属種(Simulium spp.)、ストモキシス・カルシトランス(Stomoxys calcitrans)、チプラ・パルドサ(Tipula paludosa)、
チョウ目(Lepidoptera)からは、例えば、アクロイア・グリセラ(Achroia grisella)、ガレリア・メロネラ(Galleria mellonella)、プロディア・インテルプンクテラ(Plodia interpunctella)、ティネア・クロアセラ(Tinea cloacella)、ティネア・ペリオネラ(Tinea pellionella)、ティネオラ・ビッセリエラ(Tineola bisselliella)、
ノミ目(Siphonaptera)からは、例えば、クテノセファリデス・カニス(Ctenocephalides canis)、クテノセファリデス・フェリス(Ctenocephalides felis)、ピュレクス・イリタンス(Pulex irritans)、ツンガ・ペネトランス(Tunga penetrans)、ゼノプシラ・ケオピス(Xenopsylla cheopis)、
膜翅目(Hymenoptera)からは、例えば、カンポノツス・ヘルキュレアヌス(Camponotus herculeanus)、ラシウス・フリギノサス(Lasius fuliginosus)、ラシウス・ニガー(Lasius niger)、ラシウス・ウンブラツス(Lasius umbratus)、モノモリウム・ファラオニス(Monomorium pharaonis)、パラベスピュラ種(Paravespula spp)、テトラモリウム・カエスピツム(Tetramorium caespitum)、
シラミ目(Anoplura)からは、例えば、ペディキュラス・フーマナス・カピチス(Pediculus humanus capitis)、ぺディキュラス・フーマナス・コルポリス(Pediculus humanus croporis)、ペムフィガス属種(Pemphigus spp.)、フィロエラ・バスタトリックス(Phylloera vastatrix)、フチルス・ピュービス(Phthirus pubis)、
カメムシ目(Heteroptera)からは、例えば、シメックス・ヘミプテルス(Cimex hemipterus)、シメックス・レクツラリウス(Cimex lectularius)、ロドニウス・プロリクサス(Rhodnius prolixus)、トリアトマ・インフェスタンス(Triatoma infestans)。
例(I−1)
方法A(α)
収量:0.656g(理論の73%)、logP=6.94
方法A(γ)
収量:0.117g(理論の9%)、logP=3.85
収量:149mg(理論の70%)、logP=4.45
表中に記載されているlogP値は、逆相カラム(C18)上でのHPLC(高性能液体クロマトグラフィー)により、EEC指令79/831附則V.A8に従って測定した。温度:43℃
テトラニカス・ウルチカエ(TETRUR RAUS)
溶媒:ジメチルホルムアミドの7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の10重量部
活性化合物の適切な調製物を作製するために、活性化合物の1重量部を、溶媒及び乳化剤の表記量と混合し、乳化剤を含有する水を用いて、濃縮物を所望の濃度まで希釈する。
フェドン(Phaedon)試験(PHAECO噴霧処理)
溶媒:アセトンの78.0重量部
ジメチルホルムアミドの1.5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の0.5重量部
活性化合物の適切な調製物を作製するために、活性化合物の1重量部を、溶媒及び乳化剤の表記量と混合し、乳化剤を含有する水を用いて、濃縮物を所望の濃度まで希釈する。
フランクリニエラ・オクシデンタリス(Frankliniella occidentalis)(FRANOC噴霧処理)
溶媒:アセトンの78.0重量部
ジメチルホルムアミドの1.5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の0.5重量部
活性化合物の適切な調製物を作製するために、活性化合物の1重量部を、溶媒及び乳化剤の表記量と混合し、乳化剤を含有する水を用いて、濃縮物を所望の濃度まで希釈する。アンモニウム塩の添加が必要とされる場合には、これらは、調製物のそれぞれの最終溶液の希釈後に、1000ppmの濃度で、ピペットによって添加される。
ミズス・ペルシカエ(Myzus persicae)試験(MYZUPE)
溶媒:ジメチルホルムアミドの7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の2重量部
活性化合物の適切な調製物を作製するために、活性化合物の1重量部を、溶媒及び乳化剤の表記量と混合し、乳化剤を含有する水を用いて、濃縮物を所望の濃度まで希釈する。アンモニウム塩、浸透剤又はアンモニウム塩と浸透剤の添加が必要とされる場合には、これらは、調製物のそれぞれの最終溶液の希釈後に、1000ppmの濃度で、ピペットによって添加される。
テトラニカス(Tetranychus)試験;OP耐性/浸漬処理(TETRUR)
溶媒:ジメチルホルムアミドの7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の2重量部
活性化合物の適切な調製物を作製するために、活性化合物の1重量部を、溶媒及び乳化剤の表記量と混合し、乳化剤を含有する水を用いて、濃縮物を所望の濃度まで希釈する。アンモニウム塩、浸透剤又はアンモニウム塩と浸透剤の添加が必要とされる場合には、これらは、調製物のそれぞれの最終溶液の希釈後に、1000ppmの濃度で、ピペットによって添加される。
Claims (5)
- 化合物(II)
α)式(III)の化合物
と、
又は
β)場合によって、希釈剤の存在下で、及び場合によって、酸結合剤の存在下で、式(IV)のカルボン酸無水物
と、
又は
γ)場合によって、希釈剤の存在下で、及び場合によって、酸結合剤の存在下で、式(V)の活性化されたカルボン酸誘導体
と
反応させることを特徴とする、請求項1に記載の式(I−3)の化合物を調製する方法。 - 請求項1に記載の式(I−3)の化合物を含むことを特徴とする、有害生物駆除剤。
- 請求項1に記載の式(I−3)の化合物を、有害生物、その生息環境またはその組み合わせに対して作用させることを特徴とする、有害動物を駆除する方法。
- 請求項1に記載の式(I−3)の化合物を増量剤、界面活性剤またはその組み合わせと混合することを特徴とする、有害生物駆除剤を調製する方法。
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Publication number | Priority date | Publication date | Assignee | Title |
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DE102006027730A1 (de) * | 2006-06-16 | 2007-12-20 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
DE102006027732A1 (de) * | 2006-06-16 | 2008-01-10 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
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CN102439013B (zh) * | 2009-05-19 | 2015-03-18 | 拜尔农作物科学股份公司 | 螺杂环特窗酸衍生物 |
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CN103087022B (zh) * | 2011-11-01 | 2015-06-10 | 南开大学 | 含草酰基取代的3-芳基季酮酸酯类化合物及其制备和应用 |
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Family Cites Families (34)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4014420A1 (de) | 1989-09-23 | 1991-04-04 | Bayer Ag | 5h-furan-2-on-derivate |
DE4216814A1 (de) | 1991-07-16 | 1993-01-21 | Bayer Ag | 3-aryl-4-hydroxy-(delta)(pfeil hoch)3(pfeil hoch)-dihydrofuranon- und 3-aryl-4-hydroxy-(delta)(pfeil hoch)3(pfeil hoch)-dihydrothiophenon-derivate |
AU7159994A (en) | 1993-09-17 | 1995-03-30 | Bayer Aktiengesellschaft | 3-aryl-4-hydroxy-delta3-dihydrofuranone derivatives |
DE4410420A1 (de) | 1994-03-25 | 1995-09-28 | Bayer Ag | 3-Aryl-4-hydroxy- DELTA·3·-dihydrothiophenon-Derivate |
PL322741A1 (en) | 1994-12-23 | 1998-02-16 | Bayer Ag | Derivatives of 3-arylotetronic acid, method of obtaining them, pesticides containing such derivatives and method of fighting against pests by means of them |
JP4036470B2 (ja) | 1995-02-13 | 2008-01-23 | バイエル・アクチエンゲゼルシヤフト | 除草剤および有害生物防除剤としての2−フェニル置換複素環式1,3−ケトエノール |
MX9708597A (es) | 1995-05-09 | 1998-02-28 | Bayer Ag | Cetoenoles alquil-dihalogenofenil substituidos como pesticidas y herbicidas. |
DE59609697D1 (de) | 1995-06-28 | 2002-10-24 | Bayer Ag | 2,4,5-trisubstituierte phenylketoenole zur verwendung als pestizide und herbizide |
DK0835243T3 (da) | 1995-06-30 | 2003-05-19 | Bayer Cropscience Ag | Dialkyl-halogenphenylsubstituerede ketoenoler til anvendelse som herbicider og pesticider |
EP0891330B1 (de) | 1996-04-02 | 2006-03-08 | Bayer CropScience AG | Substituierte phenylketoenole als schädlingsbekämpfungsmittel und herbizide |
CN100339352C (zh) | 1996-08-05 | 2007-09-26 | 拜尔公司 | 2-和2,5-取代的苯基酮烯醇 |
DE19651686A1 (de) | 1996-12-12 | 1998-06-18 | Bayer Ag | Neue substituierte Phenylketoenole |
DE19742492A1 (de) | 1997-09-26 | 1999-04-01 | Bayer Ag | Spirocyclische Phenylketoenole |
DE19808261A1 (de) | 1998-02-27 | 1999-10-28 | Bayer Ag | Arylphenylsubstituierte cyclische Ketoenole |
DE19813354A1 (de) | 1998-03-26 | 1999-09-30 | Bayer Ag | Arylphenylsubstituierte cyclische Ketoenole |
DE19818732A1 (de) | 1998-04-27 | 1999-10-28 | Bayer Ag | Arylphenylsubstituierte cyclische Ketoenole |
DE19901943A1 (de) * | 1999-01-20 | 2000-07-27 | Bayer Ag | Verwendung von 3-/2,4,6-Trimethylphenyl)-4-neopentylcarbonyloxy-5,5-tetramethylen- -dihydrofuran-2-on zur Bekämpfung der Weißen Fliege |
CN1272324C (zh) | 1999-09-07 | 2006-08-30 | 辛根塔参与股份公司 | 新颖的除草剂 |
DE19946625A1 (de) | 1999-09-29 | 2001-04-05 | Bayer Ag | Trifluormethylsubstituierte spirocyclische Ketoenole |
DE10016544A1 (de) | 2000-04-03 | 2001-10-11 | Bayer Ag | C2-phenylsubstituierte Ketoenole |
DE10139465A1 (de) | 2001-08-10 | 2003-02-20 | Bayer Cropscience Ag | Selektive Herbizide auf Basis von substituierten, cayclischen Ketoenolen und Safenern |
DE10239479A1 (de) | 2002-08-28 | 2004-03-04 | Bayer Cropscience Ag | Substituierte spirocyclische Ketoenole |
DE10311300A1 (de) | 2003-03-14 | 2004-09-23 | Bayer Cropscience Ag | 2,4,6-Phenylsubstituierte cyclische Ketoenole |
DE10326386A1 (de) | 2003-06-12 | 2004-12-30 | Bayer Cropscience Ag | N-Heterocyclyl-phenylsubstituierte cyclische Ketoenole |
DE10353281A1 (de) | 2003-11-14 | 2005-06-16 | Bayer Cropscience Ag | Wirkstoffkombination mit insektiziden und akariziden Eigenschaften |
DE102004011006A1 (de) | 2004-03-06 | 2005-09-22 | Bayer Cropscience Ag | Suspensionskonzentrate auf Ölbasis |
DE102004014620A1 (de) | 2004-03-25 | 2005-10-06 | Bayer Cropscience Ag | 2,4,6-phenylsubstituierte cyclische Ketoenole |
DE102004030753A1 (de) | 2004-06-25 | 2006-01-19 | Bayer Cropscience Ag | 3'-Alkoxy spirocyclische Tetram- und Tretronsäuren |
DE102004032420A1 (de) | 2004-07-05 | 2006-01-26 | Bayer Cropscience Ag | Verwendung von 3-(2,4,6-Trimethylphenyl)-4-neopentylcarbonyloxy-5,5-tetramethylen-Δ3-dihydrofuran-2-on zur Bekämpfung von Psylliden |
DE102004035133A1 (de) | 2004-07-20 | 2006-02-16 | Bayer Cropscience Ag | Selektive Insektizide auf Basis von substituierten, cyclischen Ketoenolen und Safenern |
DE102004044827A1 (de) | 2004-09-16 | 2006-03-23 | Bayer Cropscience Ag | Jod-phenylsubstituierte cyclische Ketoenole |
DE102005008021A1 (de) | 2005-02-22 | 2006-08-24 | Bayer Cropscience Ag | Spiroketal-substituierte cyclische Ketoenole |
DE102005051325A1 (de) | 2005-10-27 | 2007-05-03 | Bayer Cropscience Ag | Alkoxyalkyl spirocyclische Tetram- und Tetronsäuren |
DE102005059891A1 (de) | 2005-12-15 | 2007-06-28 | Bayer Cropscience Ag | 3'-Alkoxy-spirocyclopentyl substituierte Tetram- und Tetronsäuren |
-
2007
- 2007-01-12 DE DE102007001866A patent/DE102007001866A1/de not_active Withdrawn
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2008
- 2008-01-09 CN CN2008800018934A patent/CN101600702B/zh not_active Expired - Fee Related
- 2008-01-09 BR BRPI0806508-0A patent/BRPI0806508A2/pt not_active IP Right Cessation
- 2008-01-09 MX MX2009007436A patent/MX2009007436A/es active IP Right Grant
- 2008-01-09 WO PCT/EP2008/000084 patent/WO2008083950A2/de active Application Filing
- 2008-01-09 EP EP08701022.9A patent/EP2111398B1/de active Active
- 2008-01-09 JP JP2009545139A patent/JP5300740B2/ja not_active Expired - Fee Related
- 2008-01-09 KR KR1020097016616A patent/KR101430952B1/ko active IP Right Grant
- 2008-01-09 ES ES08701022.9T patent/ES2525481T3/es active Active
- 2008-01-09 PT PT87010229T patent/PT2111398E/pt unknown
- 2008-01-09 US US12/522,563 patent/US8247579B2/en active Active
- 2008-01-11 TW TW097101081A patent/TWI396504B/zh not_active IP Right Cessation
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Also Published As
Publication number | Publication date |
---|---|
DE102007001866A1 (de) | 2008-07-17 |
ES2525481T3 (es) | 2014-12-23 |
KR20090106410A (ko) | 2009-10-08 |
WO2008083950A3 (de) | 2008-10-16 |
US20100168226A1 (en) | 2010-07-01 |
WO2008083950A2 (de) | 2008-07-17 |
TW200836630A (en) | 2008-09-16 |
EP2111398B1 (de) | 2014-10-15 |
ZA200904745B (en) | 2010-09-29 |
WO2008083950A8 (de) | 2009-08-20 |
EP2111398A2 (de) | 2009-10-28 |
TWI396504B (zh) | 2013-05-21 |
US8247579B2 (en) | 2012-08-21 |
CN101600702A (zh) | 2009-12-09 |
MA31176B1 (fr) | 2010-02-01 |
BRPI0806508A2 (pt) | 2011-09-06 |
CL2008000079A1 (es) | 2008-05-09 |
PT2111398E (pt) | 2014-12-17 |
CN101600702B (zh) | 2013-01-02 |
KR101430952B1 (ko) | 2014-08-18 |
JP2010515697A (ja) | 2010-05-13 |
MX2009007436A (es) | 2009-07-22 |
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