JP2014534194A5 - - Google Patents

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JP2014534194A5
JP2014534194A5 JP2014535761A JP2014535761A JP2014534194A5 JP 2014534194 A5 JP2014534194 A5 JP 2014534194A5 JP 2014535761 A JP2014535761 A JP 2014535761A JP 2014535761 A JP2014535761 A JP 2014535761A JP 2014534194 A5 JP2014534194 A5 JP 2014534194A5
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chloro
imidazo
trifluoromethyl
pyridine
carboxamide
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Claims (8)

  1. 形態Aと称され、少なくとも以下の2θ反射位置
    Figure 2014534194
    を有する室温粉末Cu(Kα1)X線回折パターンにより特徴づけられる、8−クロロ−N−[(2−クロロ−5−メトキシフェニル)スルホニル]−6−(トリフルオロメチル)−イミダゾ[1,2−a]ピリジン−2−カルボキサミドの多形体。
  2. 形態TSと称され、少なくとも以下の2θ反射位置
    Figure 2014534194
    を有する室温粉末Cu(Kα1)X線回折パターンにより特徴づけられる、トルエンとの1:1溶媒和物としての8−クロロ−N−[(2−クロロ−5−メトキシフェニル)スルホニル]−6−(トリフルオロメチル)−イミダゾ[1,2−a]ピリジン−2−カルボ
    キサミドの多形体。
  3. 請求項1に記載の多形体形態Aを調製する方法であって、
    形態B、C、D、溶媒和物、非晶質形態、及び上記のいずれかと形態Aとの混合物の群から選択される8−クロロ−N−[(2−クロロ−5−メトキシフェニル)スルホニル]−6−(トリフルオロメチル)−イミダゾ[1,2−a]ピリジン−2−カルボキサミドの1種又は複数種の固体形態のスラリーを溶媒と共に形成する工程、及び8−クロロ−N−[(2−クロロ−5−メトキシフェニル)スルホニル]−6−(トリフルオロメチル)−イミダゾ[1,2−a]ピリジン−2−カルボキサミドの固体形態が多形体形態Aに転化する間前記スラリーを維持する工程を含み、
    ここで、前記溶媒が、水、C5−C8アルカン、C1−C4アルカノール、又はC3−C4ケトンを含む、上記方法。
  4. 請求項1に記載の多形体形態Aを調製する方法であって、
    (A)8−クロロ−6−トリフルオロメチル−イミダゾ[1,2−a]ピリジン−2−カルボニルクロリド又はその塩と2−クロロ−5−メトキシベンゼンスルホンアミドを、第1の溶媒の存在下で接触させて、8−クロロ−N−[(2−クロロ−5−メトキシフェニル)スルホニル]−6−(トリフルオロメチル)−イミダゾ[1,2−a]ピリジン−2−カルボキサミドの中間体固体形態を含む反応混合物を形成する工程、
    (B)8−クロロ−N−[(2−クロロ−5−メトキシフェニル)スルホニル]−6−(トリフルオロメチル)−イミダゾ[1,2−a]ピリジン−2−カルボキサミドの中間体固体形態を分離する工程、及び
    (C)8−クロロ−N−[(2−クロロ−5−メトキシフェニル)スルホニル]−6−(トリフルオロメチル)−イミダゾ[1,2−a]ピリジン−2−カルボキサミドの中間体固体形態を、任意選択で30℃から第2の溶媒の沸点の間の温度に加熱された第2の溶媒と接触させ、前記中間体固体形態を請求項1に記載の多形体形態Aに転化する工程を含み、
    ここで、前記第1の溶媒がトルエンと酢酸エチルの混合物を含み、前記第2の溶媒が、水、メタノール、アセトン、又はn−ヘプタンを含む、上記方法。
  5. (a)請求項1に記載の多形体形態A及び(b)界面活性剤、固体希釈剤、及び液体担体からなる群から選択される少なくとも1種の追加の成分を含む殺線虫性組成物。
  6. (a)請求項1に記載の多形体形態A及び(b)少なくとも1種の他の殺線虫剤、殺虫剤、又は殺真菌剤を含む殺線虫性組成物。
  7. 植物を線虫から保護する方法であって、植物、若しくはその一部、若しくはその種子に、又は前記植物の成長媒体に、殺線虫的に有効な量の、請求項1に記載の多形体形態Aを含む8−クロロ−N−[(2−クロロ−5−メトキシフェニル)スルホニル]−6−(トリフルオロメチル)−イミダゾ[1,2−a]ピリジン−2−カルボキサミドを施用することを含む方法。
  8. (b)の化合物が、アバメクチン、アセタミプリド、アクリナトリン、アミトラズ、アベルメクチン、アザジラクチン、ビフェントリン、ブプロフェジン、カルバリル、カルタップ、クロラントラニリプロール、クロルフェナピル、クロルピリホス、クロチアニジン、シアントラニリプロール、シフルトリン、ベータ−シフルトリン、シハロトリン、ガンマ−シハロトリン、ラムダ−シハロトリン、シペルメトリン、アルファ−シペルメトリン、ゼータ−シペルメトリン、シロマジン、デルタメトリン、ディルドリン、ジノテフラン、ジオフェノラン、エマメクチン、エンドスルファン、エスフェンバレレート、エチプロール、エトフェンプロックス、エトキサゾール、フェノチオカルブ、フェノキシカルブ、フェンバレレート、フィプロニル、フロニカミド、フルベンジアミド、フルフェノクスロン、フルバリネート、ホルメタナート、ヘキサフルムロン、ヒドラメチルノン、イミダクロプリド、インドキサカルブ、ルフェヌロン、メタフルミゾン、メチオカルブ、メソミル、メトプレン、メトキシフェノジド、ニテンピラム、ニチアジン、ノバルロン、オキサミル、ピメトロジン、ピレトリン、ピリダベン、ピリダリル、ピリプロキシフェン、リアノジン、スピネトラム、スピノサド、スピノジクロフェン、スピロメシフェン、スピロテトラマト、テブフェノジド、テトラメトリン、チアクロプリド、チアメトキサム、チオジカルブ、チオスルタップ−ナトリウム、トラロメトリン、トリアザメート、トリフルムロン、バチルス・チューリンゲンシス(Bacillus thuringiensis)の全株、及び核多角体病(Nucleo polyhydrosis)ウイルスの全株、からなる群から選択される、請求項6に記載の殺線虫性組成物。
JP2014535761A 2011-10-13 2012-10-05 殺線虫性スルホンアミドの固体形態 Active JP6099655B2 (ja)

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