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KR840009067A - 치환된 페닐히드록시-티오-말론산 디아미드의 제조방법 - Google Patents

치환된 페닐히드록시-티오-말론산 디아미드의 제조방법 Download PDF

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Publication number
KR840009067A
KR840009067A KR1019840001221A KR840001221A KR840009067A KR 840009067 A KR840009067 A KR 840009067A KR 1019840001221 A KR1019840001221 A KR 1019840001221A KR 840001221 A KR840001221 A KR 840001221A KR 840009067 A KR840009067 A KR 840009067A
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KR
South Korea
Prior art keywords
general formula
acid
substituted
thio
following general
Prior art date
Application number
KR1019840001221A
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English (en)
Inventor
파우스(외4) 루돌프
Original Assignee
칼-루드 비그 슈미트, 귄터 슈마허
바이엘 아크티엔게젤샤프트
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 칼-루드 비그 슈미트, 귄터 슈마허, 바이엘 아크티엔게젤샤프트 filed Critical 칼-루드 비그 슈미트, 귄터 슈마허
Publication of KR840009067A publication Critical patent/KR840009067A/ko

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Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N37/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
    • A01N37/44Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N37/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
    • A01N37/36Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N37/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
    • A01N37/44Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
    • A01N37/48Nitro-carboxylic acids; Derivatives thereof
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N47/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/02Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N25/00Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/30Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests characterised by the surfactants

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  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Agronomy & Crop Science (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • Pest Control & Pesticides (AREA)
  • Zoology (AREA)
  • General Health & Medical Sciences (AREA)
  • Environmental Sciences (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Heterocyclic Compounds Containing Sulfur Atoms (AREA)

Abstract

내용 없음

Description

치환된 페닐히드록시-티오-말론산 디아미드의 제조방법
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (3)

  1. a) 다음 일반식(Ⅱ)의 치환된 트리메틸실릴옥시페닐말론산을 무기산으로 가수분해가거나, 또는
    b) 다음 일반식(Ⅲ)의 히드록시페닐 말론산 에스테르 아미드를 암모니아와 반응시키거나, 또는
    c) 다음 일반식(Ⅳ)의 히드록시페닐 말로네이트를 암모니아와 반응시키거나, 또는
    d) 다음 일반식(Ⅴ)의 히드록시-또는 트리메틸실릴옥시페닐말론산 아미드 니트릴을 무기산으로 가수분해하거나, 또는
    e) 다음 일반식(Ⅵ)의 아크릴옥시페닐말론산 디아미드를 염기의 존재하에 가수분해가거나, 또는
    f) 다음 일반식(Ⅶ)의 아크릴옥시 페닐말론산 디니트릴을 무기 광산으로 가수분해가거나, 또는
    g) 다음 일반식(Ⅷ)의 아크릴옥시페닐말론산 디에스테르를 암모니아와 반응시켜 다음 일반식(Ⅰ)의 치환된 페닐 히드록시-티오-말론산 디아미드를 제조하는 방법.
    상기의 일반식에서, R은 m-, m´- 또는 P-위치에서 단일치환내지 삼치환된 페닐, m-또는 P-위치에서 F,C1,CH3,CF3,OCH3,OCF3,NO2또는 NH2에 의해 단일치환된 페닐을 제외한 펜타할로 게노페닐, m-, m´- 및 P-위치에서 C1에 의해 이치환된 페닐을 나타내고, Y는 0또는 s를 나타내며, R1은 임의로 치환된 알킬 또는 시클로알킬을 나타내고, R2는 R1에 대한 정의와 동일하고, R1및 R2는 동일하거나 또는 상이하며, X는 수소 또는 Si(CH3)3를 나타낸다.
  2. 적어도 일반식(Ⅰ)의 치환된 페닐히드록시-티오-말론산 디아미드 하나를 함유하는 것을 특징으로 하는 살충제.
  3. 일반식(Ⅰ)의 치환된 페닐히드록시-티오-말론산 디아미드를 중량제 및/또는 계면활성제와 함께 혼합하는 것을 특징으로 하는 살충제의 제조방법.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019840001221A 1983-03-10 1984-03-10 치환된 페닐히드록시-티오-말론산 디아미드의 제조방법 KR840009067A (ko)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DEP3308463.7 1983-03-10
DE19833308463 DE3308463A1 (de) 1983-03-10 1983-03-10 Substituierte phenylhydroxy-thio-malonsaeurediamide, verfahren zu ihrer herstellung sowie ihre verwendung als schaedlingsbekaempfungsmittel

Publications (1)

Publication Number Publication Date
KR840009067A true KR840009067A (ko) 1984-12-24

Family

ID=6193035

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019840001221A KR840009067A (ko) 1983-03-10 1984-03-10 치환된 페닐히드록시-티오-말론산 디아미드의 제조방법

Country Status (17)

Country Link
EP (1) EP0118833B1 (ko)
JP (1) JPS59170049A (ko)
KR (1) KR840009067A (ko)
AT (1) ATE18900T1 (ko)
AU (1) AU2537984A (ko)
BR (1) BR8401067A (ko)
DD (1) DD220598A5 (ko)
DE (2) DE3308463A1 (ko)
DK (1) DK145784A (ko)
ES (1) ES8500890A1 (ko)
GR (1) GR79520B (ko)
IL (1) IL71174A0 (ko)
MA (1) MA20056A1 (ko)
OA (1) OA07677A (ko)
PT (1) PT78178B (ko)
ZA (1) ZA841762B (ko)
ZW (1) ZW2184A1 (ko)

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1514709A (en) * 1974-07-30 1978-06-21 Shell Int Research Fungicidal thioamides
DE3140275A1 (de) * 1981-10-10 1983-04-28 Bayer Ag, 5090 Leverkusen Substituierte hydroxy-malonsaeurediamide, verfahren zu ihrer herstellung sowie ihre verwendung als schaedlingsbekaempfungsmittel

Also Published As

Publication number Publication date
ES530470A0 (es) 1984-11-01
DK145784A (da) 1984-09-11
DE3308463A1 (de) 1984-09-20
PT78178B (en) 1986-04-24
PT78178A (en) 1984-04-01
BR8401067A (pt) 1984-10-16
DK145784D0 (da) 1984-02-29
JPS59170049A (ja) 1984-09-26
OA07677A (fr) 1985-05-23
EP0118833A1 (de) 1984-09-19
ES8500890A1 (es) 1984-11-01
ATE18900T1 (de) 1986-04-15
AU2537984A (en) 1984-09-13
DD220598A5 (de) 1985-04-03
IL71174A0 (en) 1984-06-29
EP0118833B1 (de) 1986-04-02
ZW2184A1 (en) 1984-05-30
GR79520B (ko) 1984-10-30
DE3460066D1 (en) 1986-05-07
ZA841762B (en) 1984-10-31
MA20056A1 (fr) 1984-10-01

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PA0109 Patent application

Patent event code: PA01091R01D

Comment text: Patent Application

Patent event date: 19840310

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PC1203 Withdrawal of no request for examination
WITN Application deemed withdrawn, e.g. because no request for examination was filed or no examination fee was paid