JP2010195800A5 - - Google Patents

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JP2010195800A5
JP2010195800A5 JP2010080646A JP2010080646A JP2010195800A5 JP 2010195800 A5 JP2010195800 A5 JP 2010195800A5 JP 2010080646 A JP2010080646 A JP 2010080646A JP 2010080646 A JP2010080646 A JP 2010080646A JP 2010195800 A5 JP2010195800 A5 JP 2010195800A5
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  1. 式(I)
    Figure 2010195800
    [式中、
    は水素原子、シアノ基、ハロゲン原子、ニトロ基、(C〜C)アルキル基、1個から5個のハロゲン原子を有する(C〜C)ハロアルキル基、(C〜C)シクロアルキル基、(C〜C)アルコキシ基、1個から5個のハロゲン原子を有する(C〜C)ハロアルコキシ基、(C〜C)アルキルチオ基、1個から5個のハロゲン原子を有する(C〜C)ハロアルキルチオ基又はアミノカルボニル(C〜C)アルキル基を表し、
    は水素原子、(C〜C)アルキル基、1個から5個のハロゲン原子を有する(C〜C)ハロアルキル基、(C〜C)アルケニル基、(C〜C)シクロアルキル基、(C〜C)アルキルチオ(C〜C)アルキル基、1個から5個のハロゲン原子を有する(C〜C)ハロアルキルチオ(C〜C)アルキル基、(C〜C)アルコキシ(C〜C)アルキル基又は1個から5個のハロゲン原子を有する(C〜C)ハロアルコキシ(C〜C)アルキル基を表し、
    Gはハロゲン原子又は(C〜C)アルキル基を表し、
    Gはさらにまた(C〜C)アルキル基を表し、
    は非置換(C〜C )アルキル基を表すか又はハロゲン原子及び/又は(C〜C)シクロアルキル基からなる群から選択される同一又は異なる置換基で1置換又は多置換されている(C〜C20)アルキル基を表し、あるいは(C〜C20)アルケニル基又は(C〜C20)アルキニル基を表し、前記のアルケニル基又はアルキニル基のそれぞれはハロゲン原子及び/又は(C〜C)シクロアルキル基からなる群から選択される同一又は異なる置換基で場合によってはモノ置換又は多置換されていてもよく[但し、前記のシクロアルキル基のシクロアルキル部分はハロゲン原子及び/又は(C〜C)アルキル基からなる群から選択される同一又は異なる置換基で場合によっては1置換又は多置換されていてもよい]、且つ
    nは0、1又は2を表す]
    で示されるピラゾリルカルボキサニリド。
  2. Gがハロゲン原子又は(C〜C)アルキル基を表し且つ
    、R、R及びnが請求項1に記載の意義を有する
    ものである、請求項1に記載の式(I)で示されるピラゾリルカルボキサニリド。
  3. がメチル基を表し、
    がメチル基を表し、
    が非置換(C〜C )アルキル基を表し、
    nが0を表す
    ものである、請求項1または2に記載の式(I)で示されるピラゾリルカルボキサニリド。
  4. 請求項1に記載の式(I)で示されるピラゾリルカルボキサニリドの製造方法であって、
    式(II)
    Figure 2010195800
    (式中、R及びRは請求項1に記載の意義を有し且つ
    Xはハロゲン原子を表す)
    で示されるカルボン酸誘導体を、式(III)
    Figure 2010195800
    (式中、G、R及びnは請求項1に記載の意義を有する)
    で示されるアニリン誘導体と、
    適切ならば酸結合剤の存在下で且つ適切ならば希釈剤の存在下で反応させることを特徴とする、製造方法。
  5. 請求項1に記載の式(I)で示されるピラゾリルカルボキサニリドの製造方法であって、
    式(Ia)
    Figure 2010195800
    [式中、R、R、G及びnは請求項1に記載の意義を有し、
    は(C〜C20)アルケニル基又は(C〜C20)アルキニル基を表し、そのそれぞれはハロゲン原子及び/又は(C〜C)シクロアルキル基からなる群から選択される同一又は異なる置換基で場合によっては1置換又は多置換されていてもよく、前記のシクロアルキル基のシクロアルキル部分はハロゲン原子及び/又は(C〜C)アルキル基で場合によっては置換されていてもよい(ただし、R が非置換のアルケニル又はアルキニルである場合、そのアルケニル又はアルキニルの炭素原子数は、2〜5である)
    で示されるピラゾリルカルボキサニリドを、
    適切ならば希釈剤の存在下で且つ適切ならば触媒の存在下で水素添加することを特徴とする、製造方法。
  6. 請求項1に記載の式(I)で示されるピラゾリルカルボキサニリドの製造方法であって、
    式(IV)
    Figure 2010195800
    [式中、R、R、G及びnは請求項1に記載の意義を有し、
    はハロゲン原子及び/又は(C〜C)シクロアルキル基からなる群から選択される同一又は異なる置換基で場合によってはさらに1置換又は多置換されていてもよい(C〜C20)ヒドロキシアルキル基を表し、前記のシクロアルキル基のシクロアルキル部分はハロゲン原子及び/又は(C〜C)アルキル基で場合によっては置換されていてもよい]
    で示されるヒドロキシアルキルピラゾリルカルボキサニリドを、
    適切ならば希釈剤の存在下で且つ適切ならば酸の存在下で脱水することを特徴とする、製造方法。
  7. 請求項1に記載の式(I)で示されるピラゾリルカルボキサニリドの製造方法であって、
    式(V)
    Figure 2010195800
    (式中、R、R、G及びnは請求項1に記載の意義を有し、
    Yは臭素原子又はヨウ素原子を表す)
    で示されるハロピラゾリルカルボキサニリドを、式(VI)
    Figure 2010195800
    [式中、Rはハロゲン原子及び/又は(C〜C)シクロアルキル基からなる群から選択される同一又は異なる置換基で場合によっては1置換又は多置換されていてもよい(C〜C18)アルキル基を表し、前記のシクロアルキル基のシクロアルキル部分はハロゲン原子及び/又は(C〜C)アルキル基で場合によっては置換されていてもよい]
    で示されるアルキン、又は式(VII)
    Figure 2010195800
    [式中、R、R及びRはそれぞれ独立して水素原子を表すか、あるいはハロゲン原子及び/又は(C〜C)シクロアルキル基からなる群から選択される同一又は異なる置換基で場合によっては1置換又は多置換されていてもよいアルキル基を表し、前記のシクロアルキル基のシクロアルキル部分はハロゲン原子及び/又は(C〜C)アルキル基で場合によっては置換されていてもよいし且つ開鎖部分の炭素原子の総数は20個を超えないものとする]
    で示されるアルケンと、
    適切ならば希釈剤の存在下で、適切ならば酸結合剤の存在下で且つ1種又はそれ以上の触媒の存在下で反応させることを特徴とする、製造方法。
  8. 請求項1に記載の式(I)で示されるピラゾリルカルボキサニリドの製造方法であって、
    式(VIII)
    Figure 2010195800
    [式中、R、R、G及びnは請求項1に記載の意義を有し、
    10は水素原子を表すか、あるいはハロゲン原子及び/又は(C〜C)シクロアルキル基からなる群から選択される同一又は異なる置換基で場合によっては1置換又は多置換されていてもよい(C〜C18)アルキル基を表し、前記のシクロアルキル基のシクロアルキル部分はハロゲン原子及び/又は(C〜C)アルキル基で場合によっては置換されていてもよい]
    で示されるケトンを、一般式(IX)
    Figure 2010195800
    [式中、R11は水素原子を表すか、あるいはハロゲン原子及び/又は(C〜C)シクロアルキル基からなる群から選択される同一又は異なる置換基で場合によっては1置換又は多置換されていてもよい(C〜C18)アルキル基を表し、前記のシクロアルキル基のシクロアルキル部分はハロゲン原子及び/又は(C〜C)アルキル基で場合によっては置換されていてもよく、且つPxは−P(CCl、−P(CBr、−P(C、−P(=O)(OCH又は−P(=O)(OCを表す]
    で示されるリン化合物と
    適切ならば希釈剤の存在下で反応させることを特徴とする、製造方法。
  9. 請求項1に記載の式(I)で示されるピラゾリルカルボキサニリドの少なくとも1つと、その他に増量剤及び/又は界面活性剤とを含有してなることを特徴とする、農園芸用殺菌組成物。
  10. 式(IV)
    Figure 2010195800
    [式中、R、R、G及びnは請求項1または2に記載の意義を有し且つRはハロゲン原子及び/又は(C〜C)シクロアルキル基からなる群から選択される同一又は異なる置換基で場合によっては1置換又は多置換されていてもよい(C〜C20)ヒドロキシアルキル基を表し、前記のシクロアルキル基のシクロアルキル部分はハロゲン原子及び/又は(C〜C)アルキル基で場合によっては置換されていてもよい]
    で示されるヒドロキシアルキルピラゾリルカルボキサニリド。
  11. 式(V)
    Figure 2010195800
    (式中、R、R、G及びnは請求項1または2に記載の意義を有し且つYは臭素原子又はヨウ素原子を表す)
    で示されるハロピラゾリルカルボキサニリド。
  12. 式(VIII)
    Figure 2010195800
    [式中、R、R、G及びnは請求項1または2に記載の意義を有し且つ
    10は水素原子を表すかあるいはハロゲン原子及び/又は(C〜C)シクロアルキル基からなる群から選択される同一又は異なる置換基で場合によっては1置換又は多置換されていてもよい(C〜C18)アルキル基を表し、前記のシクロアルキル基のシクロアルキル部分はハロゲン原子及び/又は(C〜C)アルキル基で場合によっては置換されていてもよい]
    で示されるケトン。
JP2010080646A 2001-07-25 2010-03-31 殺菌剤としてのピラゾリルカルボキサニリド Expired - Lifetime JP5204799B2 (ja)

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DE10136065A DE10136065A1 (de) 2001-07-25 2001-07-25 Pyrazolylcarboxanilide
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US (1) US7538073B2 (ja)
EP (1) EP1414803B1 (ja)
JP (3) JP4550412B2 (ja)
KR (2) KR101070880B1 (ja)
CN (1) CN1255384C (ja)
BR (1) BR0211482B1 (ja)
DE (1) DE10136065A1 (ja)
DK (1) DK1414803T3 (ja)
ES (1) ES2399354T3 (ja)
HU (1) HU230165B1 (ja)
IL (2) IL159839A0 (ja)
MX (1) MXPA04000622A (ja)
NL (1) NL350069I2 (ja)
PL (1) PL216069B1 (ja)
PT (1) PT1414803E (ja)
TW (1) TWI317357B (ja)
WO (1) WO2003010149A1 (ja)

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