KR950011415A - 나프틸 에테르, 이의 제조 방법, 이를 함유하는 조성물 및 이의 용도 - Google Patents

나프틸 에테르, 이의 제조 방법, 이를 함유하는 조성물 및 이의 용도 Download PDF

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KR950011415A
KR950011415A KR1019940025822A KR19940025822A KR950011415A KR 950011415 A KR950011415 A KR 950011415A KR 1019940025822 A KR1019940025822 A KR 1019940025822A KR 19940025822 A KR19940025822 A KR 19940025822A KR 950011415 A KR950011415 A KR 950011415A
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oxygen
unsubstituted
compound
nitrogen
formula
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그라메노스 바실리오스
키르스트겐 라인하르트
쾨니히 하르트만
오베르도르프 클라우스
자우터 휘베르트
로렌츠 기젤라
암메르만 에베르하르트
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빅케, 라이씽거
바스프 악티엔게젤샤프트
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Publication of KR950011415A publication Critical patent/KR950011415A/ko

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Abstract

하기 일반식(Ⅰ)의 나프틸 에테르, 이의 제조 방법, 이를 함유하는 조성물 및 해충 또는 해로운 진균을 방제하기 위한 용도가 기술되어 있다.
상기 식에서, A는 탄소 고리원 이외에 추가의 고리원으로서 1 내지 3개의 질소 원자 또는 1 또는 2개의 질소 원자 및 산소 또는 황 원자, 또는 산소 또는 황 원자를 함유하 수 있는 비치환되거나 또는 치환된 페닐 또는 비치환 되거나 치환된 5-내지 6-원 헤테로아릴이며; n은 0 또는 1이고; x는 산소, 황 또는 질소이며, 이때 질소 원자는 수소, C1-C4-알킬, C1-C4-알콕시, C3-C6-시클로알킬, 비치환되거나 또는 치환된 페닐 또는 비치환되거나 또는 치환된 벤질기 중 어느 하나를 함유할 수 있고; Y는 산소이거나, 또는 Z가 NOCH3인 경우에는, 산소 또는 질소이며, 이때 질소 원자는 수소, C1-C4-알킬 또는 C1-C4-알콕시기 중 어느 하나를 함유할 수 있고: Z는 CHOCH3, NOCH3, CHCH3또는 CHCH2CH3이고; R1은 C1-C4-알킬이고; R2는 비치환되거나 또는 치환된 C1-C6-알킬, C3-C6-시클로알킬, C2-C6-알케닐 또는 C3-C6-알키닐; 비치환되거나 또는 치환된 페닐; 탄소 고리원이외에 추가의 고리원으로서 1 내지 3개의 질소 원자 또는 1 또는 2개의 질소 원자 및 산소 또는 황 원자를 함유하는 비치환되거나 또는 치환된 5-또는 6-원 헤테로아일; 또는 n이 0인 경우 상기에서 정의된 기이외에 추가로 할로겐, C1-C6-알콕시, C1-C4-알킬설폭실 또는 페닐설폭실(이때 페닐 고리는 또한 치환체를 함유할 수 있다)이다.

Description

나프틸 에테르, 이의 제조 방법, 이를 함유하는 조성물 및 이의 용도
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (10)

  1. 하기 일반식(Ⅰ)의 나프틸 에테르,
    상기 식에서, A는 탄소 고리원 이외에 추가의 고리원으로서 1 내지 3개의 질소 원자 또는 1 또는 2개의 질소 원자 및 산소 또는 황 원자, 또는 산소 또는 황 원자를 함유하 수 있는 비치환되거나 또는 치환된 페닐 또는 비치환 되거나 치환된 5-내지 6-원 헤테로아릴이며; n은 0 또는 1이고; x는 산소, 황 또는 질소이며, 이때 질소 원자는 수소, C1-C4-알킬, C1-C4-알콕시, C3-C6-시클로알킬, 비치환되거나 또는 치환된 페닐 또는 비치환되거나 또는 치환된 벤질기 중 어느 하나를 함유할 수 있고; Y는 산소이거나, 또는 Z가 NOCH3인 경우에는, 산소 또는 질소이며, 이때 질소 원자는 수소, C1-C4-알킬 또는 C1-C4-알콕시기 중 어느 하나를 함유할 수 있고: Z는 CHOCH3, NOCH3, CHCH3또는 CHCH2CH3이고; R1은 C1-C4-알킬이고; R2는 비치환되거나 또는 치환된 C1-C6-알킬, C3-C6-시클로알킬, C2-C6-알케닐 또는 C3-C6-알키닐; 비치환되거나 또는 치환된 페닐; 탄소 고리원이외에 추가의 고리원으로서 1 내지 3개의 질소 원자 또는 1 또는 2개의 질소 원자 및 산소 또는 황 원자를 함유하는 비치환되거나 또는 치환된 5-또는 6-원 헤테로아일; 또는 n이 0인 경우 상기에서 정의된 기이외에 추가로 할로겐, C1-C6-알콕시, C1-C4-알킬설폭실 또는 페닐설폭실(이때 페닐 고리는 또한 치환체를 함유할 수 있다)이다.
  2. 제1항에 있어서, 치환체 A가 비치환되거나 또는 치환된 페닐, 푸릴, 티에닐, 피롤릴, 피라졸릴, 아미다졸릴, 트리아졸릴, 이속사졸릴, 옥사졸릴, 옥사디아볼릴, 이소티아졸릴, 티아졸릴, 티아디아졸릴, 피리딜, 피리다지닐, 피리미딜, 피라지닐 또는 트리아지닐이고, 인접한 기 (X)n또는 0와의 결합은 2개의 메타-또는 슈도-메타 탄소 고리원을 통해 이루어진 것인 일반식(Ⅰ)의 화합물.
  3. 제1항에 있어서, Y가 산소이고, Z가 CHOCH3, NOCH3또는 CHCH3인 일반식(Ⅰ)의 화합물.
  4. 제1항에 있어서, Y가 NH이고, Z가 NOCH3인 일반식(Ⅰ)의 화합물.
  5. 제3항 내지 4항에 있어서, n이 1이고 R2가 비치환되거나 또는 치환된 페닐인 일반식(Ⅰ)의 화합물.
  6. 제1항에서 청구한 일반식(Ⅰ)의 화합물 유효량 및 통상의 첨가제를 함유하는 해충 또는 해로운 진균을 방제하기 위한 조성물.
  7. 제6항에 있어서, 고충강, 거미강 및 선충강의 해충을 방제하기 위한 것이 조성물.
  8. 해충 또는 해로운 진균, 이들의 서식지 또는 이들을 없애고자 하는 식물, 표면, 물자 또는 공간을 제1항에서 청구한 일반식(Ⅰ)의 화합물 유효량으로 처리함을 포함하여 해충 또는 해로운 진균을 방제하는 방법.
  9. 해충 또는 해로운 진균을 방제하기 위한 조성물을 제조하기 위해 제1항에서 청구한 일반식(Ⅰ)의 화합물을 사용하는 방법.
  10. 해충 또는 해로운 진균을 방제하기 위해 제1항에서 청구한 일반식(Ⅰ)의 화합물을 사용하는 방법.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019940025822A 1993-10-12 1994-10-10 나프틸 에테르, 이의 제조 방법, 이를 함유하는 조성물 및 이의 용도 KR950011415A (ko)

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CN (1) CN1107141A (ko)
AT (1) ATE204259T1 (ko)
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DE19646407A1 (de) * 1996-11-11 1998-05-14 Bayer Ag Halogenpyrimidine
DE10211428A1 (de) * 2002-03-15 2003-10-23 Bayer Ag Bekämpfung von Parasiten an Tieren durch Halogenpyrimidine
JP2006504667A (ja) * 2002-08-08 2006-02-09 ベーリンガー インゲルハイム ファーマシューティカルズ インコーポレイテッド 炎症過程に関与するサイトカインの抑制剤としてのフッ素化フェニル−ナフタレニル−尿素化合物

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DE3025368A1 (de) * 1980-07-04 1982-01-28 Hoechst Ag, 6000 Frankfurt Verfahren zur synthese von strobilurin
DE3623921A1 (de) * 1986-07-16 1988-01-21 Basf Ag Oximether und diese enthaltende fungizide
GB8617648D0 (en) * 1986-07-18 1986-08-28 Ici Plc Fungicides
DE3843439A1 (de) * 1988-12-23 1990-06-28 Basf Ag Schwefelhaltige oximether und diese enthaltende fungizide
DE3906160A1 (de) * 1989-02-28 1990-10-11 Basf Ag Ortho-substituierte 1-naphthylether und diese enthaltende fungizide
GB9016584D0 (en) * 1990-07-27 1990-09-12 Ici Plc Fungicides
DE4116090A1 (de) * 1991-05-17 1992-11-19 Basf Ag (alpha)-phenylacrylsaeurederivate, verfahren zu ihrer herstellung und ihre verwendung zur bekaempfung von schaedlingen und schadpilzen
DE4117371A1 (de) * 1991-05-28 1992-12-03 Basf Ag Antimykotische mittel, die phenylessigsaeurederivate enthalten
DE4140558A1 (de) * 1991-12-09 1993-06-17 Bayer Ag Substituierte oximetheramide

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ATE204259T1 (de) 2001-09-15
CA2117837A1 (en) 1995-04-13
CN1107141A (zh) 1995-08-23
JPH07188113A (ja) 1995-07-25
EP0647631B1 (de) 2001-08-16
EP0647631A1 (de) 1995-04-12
DE59409830D1 (de) 2001-09-20

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