JP2006515285A - 置換されたピリジルオキシアルキルアミド類及びそれらの殺菌剤としての使用 - Google Patents
置換されたピリジルオキシアルキルアミド類及びそれらの殺菌剤としての使用 Download PDFInfo
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Abstract
Description
R1は、直鎖C1-4アルキル基(例えばメチル、エチル、n-プロピル及びn-ブチル)であり;
R2は、H、C1-4アルキル、C1-4アルコキシメチル又はベンジルオキシメチル(ここでベンジル部位のフェニル環は任意にC1-4アルコキシで置換され)であり;
R3及びR4は、両方が揃ってHではなく、そして両方がH以外である場合、それらの結合した総炭素原子は4を超えないことを条件として、独立してH、C1-3アルキル、C2-3アルケニル又はC2-3アルキニルであるが、或いは
R3及びR4は、任意に1個のO、S又はN原子を含む3又は4員炭環を形成するためにそれらを結合した炭素原子に連結し、そして任意にハロゲン又はC1-4アルキルで置換され;そして
R5はH、C1-4アルキル又はC3-6シクロアルキルであり(ここでアルキル又はシクロアキル基は、ハロゲン、ヒドロキシ、C1-6アルコキシ、シアノ、C1-4アルキルカルボニルオキシ、アミノカルボニルオキシ、モノ-又はジ(C1-4)アルキルアミノカルボニルオキシ、-S(O)n(C1-6)アルキル(ここでnは0、1又は2であり)、トリアゾリル(例えば1,2,4-トリアゾール-1-イル)、トリ(C1-4)アルキルシリルオキシ、任意に置換されたフェノキシ、任意に置換されたチエニルオキシ、任意に置換されたベンジルオキシ又は任意に置換されたチエニルメトキシにより任意に置換され、或いは
R5は任意に置換されたフェニル、任意に置換されたチエニル又は任意に置換されたベンジルであり;
ここで任意に置換されたX、Y及びR5官能基(values)のフェニル及びチエニル環は、ハロゲン、ヒドロキシ、メルカプト、C1-4アルキル、C2-4アルケニル、C2-4アルキニル、C1-4アルコキシ、C2-4アルケニルオキシ、C2-4アルキニルオキシ、ハロ(C1-4)アルキル、ハロ(C1-4)アルコキシ、C1-4アルキルチオ、ハロ(C1-4)アルキルチオ、ヒドロキシ(C1-4)-アルキル、C1-4アルコキシ(C1-4)アルキル、C3-6シクロアルキル、C3-6シクロアルキル(C1-4)アルキル、フェノキシ、ベンジルオキシ、ベンゾイルオキシ、シアノ、イソシアノ、チオシアネート、イソチオシアネート、ニトロ、-NRmRn、-NHCORm、-NHCONRmRn、-CONRmRn、-SO2Rm、-OSO2Rm、-CORm、-CRm=NRn又は-N=CRmRn(ここでRm及びRnは独立して水素、C1-4アルキル、ハロ(C1-4)アルキル、C1-4アルコキシ、ハロ(C1-4)アルコキシ、C1-4アルキルチオ、C3-6シクロアルキル、C3-6シクロアルキル(C1-4)アルキル、フェニル又はベンジル(当該フェニル及びベンジル基は、ハロゲン、C1-4アルキル又はC1-4アルコキシにより任意に置換され))から選定された1、2又は3個の置換基により任意に置換される。
ml=ミリリットル
DMSO=ジメチルスルホキシド
g=グラム
NMR=核磁器共鳴
ppm=百万分の1
HPLC=高速液体クロマトグラフィー
M+=マスイオン
s =シングレット
t=トリプレット
br s=ブロードシングレット
q=クォーテット
d=ダブレット
m=マルチプレット
dd=ダブル ダブレット
ppm=百万分の1
ステップ1
t-ブトキシドカリウム(2.4g)をt-ブチルアルコール(130ml)中へ溶解した。当該混合物を30分間室温で撹拌し、その後5-クロロピリジノール(2.0g)を付加し、引き続きエチル2-クロロ-2-エトシキアセテート(3.14g、純度90%)を付加し、そして触媒量のヨウ化カリウム(0.005g)を付加した。当該反応物は、ピンクオレンジになり、塩化カリウムが沈殿した。当該反応物を、その後18時間貯蔵し、そして水へ注ぎ、そしてクロロホルムで抽出した。有機相を分離し食塩水で洗浄し、硫酸マグネシウムで乾燥させ、そして無色のオイルを与えるために蒸発させ、シリカゲル(40-60)上のフラッシュカラムクロマトグラフィーによりエチルアセテート/ヘキサン(1:4)を用いて溶出し、無色のオイルとして要求される生産物(3.08g)を与えるために精製した。
1H NMR (CDCl3)δppm : 1.27 (3H, t); 1.31 (3H, t); 3.75 (1H, m) ; 3.83 (lH, m); 4.30 (2H, q); 5.33 (lH, s); 7.46 (lH, t); 8.30 (lH, d); 8.35 (lH, d).
室温でメタノール(5ml)中のエチル2-(5-クロロピリジル-3-オキシ)-2-(エトシキ)アセテート(0.45g)へ水中(1.5ml)の水酸化ナトリウム(0.076g)の溶液を付加した。当該反応物を5分間撹拌し、メタノールを蒸発させ、残留物をエチルアセテートで洗浄した。その後水性フラクションを塩酸で酸性化し、そしてエチルアセテートにより抽出した。当該エチルアセテートフラクションを硫酸マグネシウムで乾燥させ、そして更なる精製なしで使用されるペイルイエローガム(0.40g)として、2-(5-クロロピリジル-3-オキシ)-2-(エトシキ)酢酸を与えるために蒸発させた。
1H NMR(CDC13)δppm : 1.30 (3H, t); 3.78(lH, m); 3.90 (lH, m); 5.59 (lH, s); 7.60 (lH, s); 8.30 (lH, d), 8.40(lH, d).
トリエチルアミン(0.30ml)をDMF(8 ml)中で撹拌された4-アミノ-4-メチル-ペント-2-インハイドロクロライド(0.231g)へ付加し、白色の懸濁物を与えた。2-(5-クロロピリジル-3-オキシ)-2-(エトシキ)酢酸(0.40g)を引き続き、触媒量の1-ヒドロキシベンゾトリアゾール(0.005g)及びN-(3-ジメチルアミノプロピル)-N'-エチルカルボジイミドハイドロクロライド(0.332g)へ付加した。白色懸濁物を室温で18時間撹拌し、水を付加し、そして当該水性相をエチルアセテートにより抽出した。当該有機相を水、飽和炭酸水素ナトリウムで洗浄し、その後食塩水で洗浄し、硫酸マグネシウムで乾燥させ、そして黄色オイルを与えるため蒸発させ、シリカゲル(40-60)上のフラッシュカラムクロマトグラフィーで、エチルアセテート/ヘキサン(1:4)により溶出し、無色のオイル(0.130g)として要求される生産物を与えるために精製した。
1H NMR (CDC13)δppm : 1.30 (3H, t); 1.62 (3H, s); 1.63 (6H, s); 3.67(1H, m); 1.82 (3H, s); 3.70 (lH, m); 3.88(lH, m); 5.32(lH, s); 6.71(1H, brs); 7.53(lH, dd); 8.29(lH, d); 8.35(lH, d)。
Plasmopara viticola、化合物1 (1)、1 (9)、1 (13);Phytophthora infestans、化合物1 (1)、1 (9)、1 (17);Erysiphe graminis f.sp. hordei,化合物 1(1);Erysiphe graminis f.sp. tritici, 化合物 1 (13);Septoria tritici、化合物 1 (9)。
Claims (12)
- 一般式(1)の化合物:
Rlは、直鎖C1-4アルキル基であり;
R2は、H、C1-4アルキル、C1-4アルコキシメチル、又はベンジルオキシメチル(ここでベンジル部位のフェニル環は任意にC1-4アルコキシで置換され)であり、;
R3及びR4は、両方が揃ってHではなく、そして両方がH以外である場合、それらの結合した総炭素原子は4を超えないことを条件として、独立してH、C1-3アルキル、C2-3アルケニル又はC2-3アルキニルであり、或いは
R3及びR4は、任意に1個のO、S又はN原子を含む3又は4員炭環を形成するためにそれらの結合した炭素原子に連結し、そして任意にハロゲン又はC1-4アルキルで置換され;そして
R5はH、C1-4アルキル又はC3-6シクロアルキルであり(ここでアルキル又はシクロアキル基は、ハロゲン、ヒドロキシ、C1-6アルコキシ、シアノ、C1-4アルキルカルボニルオキシ、アミノカルボニルオキシ、モノ-又はジ(C1-4)アルキルアミノカルボニルオキシ、-S(O)n(C1-6)アルキル(ここでnは0、1又は2であり)、トリアゾリル、トリ(C1-4)アルキルシリルオキシ、任意に置換されたフェノキシ、任意に置換されたチエニルオキシ、任意に置換されたベンジルオキシ又は任意に置換されたチエニルメトキシにより任意に置換され)、或いは
R5は任意に置換されたフェニル、任意に置換されたチエニル又は任意に置換されたベンジルである(ここで任意に置換されたX、Y及びR5官能基(values)のフェニル及びチエニル環は、ハロゲン、ヒドロキシ、メルカプト、C1-4アルキル、C2-4アルケニル、C2-4アルキニル、C1-4アルコキシ、C2-4アルケニルオキシ、C2-4アルキニルオキシ、ハロ(C1-4)アルキル、ハロ(C1-4)アルコキシ、C1-4アルキルチオ、ハロ(C1-4)アルキルチオ、ヒドロキシ(C1-4)-アルキル、C1-4アルコキシ(C1-4)アルキル、C3-6シクロアルキル、C3-6シクロアルキル(C1-4)アルキル、フェノキシ、ベンジルオキシ、ベンゾイルオキシ、シアノ、イソシアノ、チオシアネート、イソチオシアネート、ニトロ、-NRmRn、-NHCORm、-NHCONRmRn、-CONRmRn、-SO2Rm、-OSO2Rm、-CORm、-CRm=NRn、又は-N=CRmRn(ここでRm及びRnは独立して水素、C1-4アルキル、ハロ(C1-4)アルキル、C1-4アルコキシ、ハロ(C1-4)アルコキシ、C1-4アルキルチオ、C3-6シクロアルキル、C3-6シクロアルキル(C1-4)アルキル、フェニル又はベンジルであり(当該フェニル及びベンジル基は、ハロゲン、C1-4アルキル又はC1-4アルコキシにより任意に置換され))から選定された、1、2又は3個の置換基により任意に置換される)。 - 前記Xが塩素又は臭素であり、そしてYがHである、請求項1に記載の化合物。
- 前記R1がメチル、エチル、n−プロピル、又はn−ブチルである、請求項1又は2に記載の化合物。
- 前記R1がメチル又はエチルである、請求項1から3のいずれか1項に記載の化合物。
- 前記R2がHである、請求項1から4のいずれか1項に記載の化合物。
- 前記R3及びR4が共にメチルである、請求項1から5のいずれか1項に記載の化合物。
- 前記R5がH、メチル、ヒドロキシメチル、メトキシメチル、1−メトキシエチル、tert-ブチルジメチルシリルオキシメチル、3−シアノプロピル、3−(1,2,4−トリアゾール−1−イル)プロピル、3−メチルチオプロピル、3−メタンスルフィニルプロピル、又は3−メタンスルホニルプロピルである、請求項1から6のいずれか1項に記載の化合物。
- 前記X及びYが独立してハロゲン、C1-4アルキル、C2-4アルケニル、C2-4アルキニル、任意に置換されたフェニル、シアノ、又は-COR’である請求項1に記載の化合物
(式中、R’はHもしくはC1-4アルキルであり、又はYはHであり;
R1は、直鎖C1-4アルキル基であり;
R2はH、C1-4アルキル、C1-4アルコキシメチル、又はベンジルオキシメチル(ここでベンジル部位のフェニル環は任意にC1-4アルコキシで置換され)であり;
R3及びR4は、両方が揃ってHではなく、そして両方がH以外である場合、それらの結合した総炭素原子は4を超えないことを条件として、独立してH、C1-3アルキル、C2-3アルケニル又はC2-3アルキニルであり、或いは
R3及びR4は、任意に1個のO、S又はN原子を含む3又は4員炭環を形成するためにそれらの結合した炭素原子に連結し、そして任意にハロゲン又はC1-4アルキルで置換され;そして
R5はH、C1-4アルキル又はC3-6シクロアルキルであり(ここで当該アルキル又はシクロアルキル基はハロゲン、ヒドロキシ、C1-6アルコキシ、C1-6アルキルチオ、シアノ、C1-4アルキルカルボニルオキシ、アミノカルボニルオキシ、又はモノ-又はジ(C1-4)アルキルアミノカルボニルオキシ、トリ(C1-4)アルキルシリルオキシ、任意に置換されたフェノキシ、任意に置換されたチエニルオキシ、任意に置換されたベンジルオキシ又は任意に置換されたチエニルメトキシにより任意に置換され)或いは
R5は、任意に置換されたフェニル、任意に置換されたチエニル又は任意に置換されたベンジルである;
(ここで任意に置換されたX、Y及びR5官能基のフェニル及びチエニル環は、ハロゲン、ヒドロキシ、メルカプト、C1-4アルキル、C2-4アルケニル、C2-4アルキニル、C1-4アルコキシ、C2-4アルケニルオキシ、C2-4アルキニルオキシ、ハロ(C1-4)アルキル、ハロ(C1-4)アルコキシ、C1-4アルキルチオ、ハロ(C1-4)アルキルチオ、ヒドロキシ(C1-4)アルキル、C1-4アルコキシ(C1-4)アルキル、C3-6シクロアルキル、C3-6シクロアルキル(C1-4)アルキル、フェノキシ、ベンジルオキシ、ベンゾイルオキシ、シアノ、イソシアノ、チオシアネート、イソチオシアネート、ニトロ、-NRmRn、-NHCORm、-NHCONRmRn、-CONRmRn、-SO2Rm、-OSO2Rm、-CORm、-CRm=NRn又は-N=CRmRn(式中Rm及びRnは独立して水素、C1-4アルキル、ハロ(C1-4)アルキル、C1-4アルコキシ、ハロ(C1-4)アルコキシ、C1-4アルキルチオ、C3-6シクロアルキル、C3-6シクロアルキル(C1-4)アルキル、フェニル又はベンジルである(当該フェニル及びベンジル基は任意にハロゲン、C1-4アルキル又はC1-4アルコキシにより置換される))から選定された1、2又は3個の置換基により任意に置換される))。 - 前記Xが塩素又は臭素であり、及びYがHであり;R1がメチル、エチル、n−プロピル、n−ブチルであり;R2がHであり;R3及びR4が共にメチルであり;並びにR5はH、メチル、ヒドロキシメチル、メトキシメチル、1-メトキシエチル、tert-ブチルジメチルシリルオキシメチル、3−メチルチオプロピル、3−メタンスルフィニルプロピル、又は3−メタンスルホニルプロピルである、請求項1に記載の化合物。
- 本明細書において記載される請求項1に記載の化合物の調整方法。
- 請求項1に定義されるような式(1)の化合物の殺菌剤的効果量、及びそれらのための適した担体又は希釈剤を含む殺菌組成物。
- 請求項1に定義されるような式(1)の化合物、或いは植物、植物の種、植物もしくは種の所在箇所、又は土壌もしくは任意の他の植物成長媒体に請求項11に記載の組成物の殺菌剤的効果量を適用させることを含む、植物病原菌類と戦う又は植物病原菌類を制御するための方法。
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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GBGB0227554.3A GB0227554D0 (en) | 2002-11-26 | 2002-11-26 | Fungicides |
PCT/GB2003/004547 WO2004048337A1 (en) | 2002-11-26 | 2003-10-23 | Substituted pyridyloxyalkylamides and their use as fungicides |
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JP2006515285A true JP2006515285A (ja) | 2006-05-25 |
JP2006515285A5 JP2006515285A5 (ja) | 2008-01-10 |
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JP2004554635A Pending JP2006515285A (ja) | 2002-11-26 | 2003-10-23 | 置換されたピリジルオキシアルキルアミド類及びそれらの殺菌剤としての使用 |
Country Status (16)
Country | Link |
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US (1) | US7511151B2 (ja) |
EP (1) | EP1567499B1 (ja) |
JP (1) | JP2006515285A (ja) |
KR (1) | KR20050083991A (ja) |
CN (1) | CN100336808C (ja) |
AR (1) | AR042136A1 (ja) |
AT (1) | ATE413387T1 (ja) |
AU (1) | AU2003274351A1 (ja) |
BR (1) | BR0316529A (ja) |
CA (1) | CA2502156A1 (ja) |
DE (1) | DE60324586D1 (ja) |
ES (1) | ES2316810T3 (ja) |
GB (1) | GB0227554D0 (ja) |
MX (1) | MXPA05005452A (ja) |
PL (1) | PL376843A1 (ja) |
WO (1) | WO2004048337A1 (ja) |
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GB0129267D0 (en) * | 2001-12-06 | 2002-01-23 | Syngenta Ltd | Fungicides |
GB0227556D0 (en) | 2002-11-26 | 2002-12-31 | Syngenta Ltd | Fungicides |
GB0227555D0 (en) * | 2002-11-26 | 2002-12-31 | Syngenta Ltd | Fungicides |
GB0227558D0 (en) * | 2002-11-26 | 2002-12-31 | Syngenta Ltd | Fungicides |
GB0227554D0 (en) | 2002-11-26 | 2002-12-31 | Syngenta Ltd | Fungicides |
GB0227551D0 (en) | 2002-11-26 | 2002-12-31 | Syngenta Ltd | Fungicides |
GB0312863D0 (en) * | 2003-06-04 | 2003-07-09 | Syngenta Ltd | Fungicides |
GB0312864D0 (en) * | 2003-06-04 | 2003-07-09 | Syngenta Ltd | Fungicides |
GB0426372D0 (en) * | 2004-12-01 | 2005-01-05 | Syngenta Ltd | Fungicides |
GB0426373D0 (en) | 2004-12-01 | 2005-01-05 | Syngenta Ltd | Fungicides |
CN103694197B (zh) * | 2014-01-09 | 2015-07-15 | 华中师范大学 | 苯氧乙酰胺类化合物及其制备方法与应用 |
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WO1998018766A1 (fr) * | 1996-10-31 | 1998-05-07 | Kumiai Chemical Industry Co., Ltd. | Derives d'amine pyrimidinyloxyalcanoique et fongicides pour usage agricole et horticole |
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GB0227555D0 (en) * | 2002-11-26 | 2002-12-31 | Syngenta Ltd | Fungicides |
GB0227554D0 (en) | 2002-11-26 | 2002-12-31 | Syngenta Ltd | Fungicides |
GB0227558D0 (en) * | 2002-11-26 | 2002-12-31 | Syngenta Ltd | Fungicides |
GB0227557D0 (en) * | 2002-11-26 | 2002-12-31 | Syngenta Ltd | Fungicides |
GB0227556D0 (en) * | 2002-11-26 | 2002-12-31 | Syngenta Ltd | Fungicides |
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GB0312863D0 (en) * | 2003-06-04 | 2003-07-09 | Syngenta Ltd | Fungicides |
GB0312864D0 (en) | 2003-06-04 | 2003-07-09 | Syngenta Ltd | Fungicides |
GB0426372D0 (en) | 2004-12-01 | 2005-01-05 | Syngenta Ltd | Fungicides |
GB0426373D0 (en) | 2004-12-01 | 2005-01-05 | Syngenta Ltd | Fungicides |
-
2002
- 2002-11-26 GB GBGB0227554.3A patent/GB0227554D0/en not_active Ceased
-
2003
- 2003-10-23 WO PCT/GB2003/004547 patent/WO2004048337A1/en active Application Filing
- 2003-10-23 ES ES03758336T patent/ES2316810T3/es not_active Expired - Lifetime
- 2003-10-23 DE DE60324586T patent/DE60324586D1/de not_active Expired - Lifetime
- 2003-10-23 MX MXPA05005452A patent/MXPA05005452A/es active IP Right Grant
- 2003-10-23 AU AU2003274351A patent/AU2003274351A1/en not_active Abandoned
- 2003-10-23 EP EP03758336A patent/EP1567499B1/en not_active Expired - Lifetime
- 2003-10-23 JP JP2004554635A patent/JP2006515285A/ja active Pending
- 2003-10-23 CA CA002502156A patent/CA2502156A1/en not_active Abandoned
- 2003-10-23 PL PL376843A patent/PL376843A1/pl not_active Application Discontinuation
- 2003-10-23 BR BR0316529-9A patent/BR0316529A/pt not_active IP Right Cessation
- 2003-10-23 US US10/536,461 patent/US7511151B2/en not_active Expired - Fee Related
- 2003-10-23 KR KR1020057009580A patent/KR20050083991A/ko not_active Application Discontinuation
- 2003-10-23 CN CNB2003801036250A patent/CN100336808C/zh not_active Expired - Fee Related
- 2003-10-23 AT AT03758336T patent/ATE413387T1/de not_active IP Right Cessation
- 2003-11-24 AR ARP030104338A patent/AR042136A1/es unknown
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AR042136A1 (es) | 2005-06-08 |
US20060148859A1 (en) | 2006-07-06 |
BR0316529A (pt) | 2005-10-04 |
PL376843A1 (pl) | 2006-01-09 |
CN100336808C (zh) | 2007-09-12 |
ATE413387T1 (de) | 2008-11-15 |
GB0227554D0 (en) | 2002-12-31 |
MXPA05005452A (es) | 2005-08-26 |
EP1567499B1 (en) | 2008-11-05 |
DE60324586D1 (de) | 2008-12-18 |
KR20050083991A (ko) | 2005-08-26 |
CA2502156A1 (en) | 2004-06-10 |
AU2003274351A1 (en) | 2004-06-18 |
ES2316810T3 (es) | 2009-04-16 |
US7511151B2 (en) | 2009-03-31 |
CN1714080A (zh) | 2005-12-28 |
EP1567499A1 (en) | 2005-08-31 |
WO2004048337A1 (en) | 2004-06-10 |
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