DK2571887T3 - Fremgangsmåde til fremstilling af dithiin-tetracarboxy-diimider - Google Patents

Fremgangsmåde til fremstilling af dithiin-tetracarboxy-diimider Download PDF

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Publication number
DK2571887T3
DK2571887T3 DK11719280.7T DK11719280T DK2571887T3 DK 2571887 T3 DK2571887 T3 DK 2571887T3 DK 11719280 T DK11719280 T DK 11719280T DK 2571887 T3 DK2571887 T3 DK 2571887T3
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Denmark
Prior art keywords
sulphide
alkyl
hydrogen
halogen
formula
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DK11719280.7T
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English (en)
Inventor
Thomas Himmler
Ymann Martin Kau
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Bayer Cropscience Ag
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Publication of DK2571887T3 publication Critical patent/DK2571887T3/da

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/44Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having three double bonds between ring members or between ring members and non-ring members
    • C07D207/444Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having three double bonds between ring members or between ring members and non-ring members having two doubly-bound oxygen atoms directly attached in positions 2 and 5
    • C07D207/456Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having three double bonds between ring members or between ring members and non-ring members having two doubly-bound oxygen atoms directly attached in positions 2 and 5 with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to other ring carbon atoms
    • 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
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/02Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
    • A01N43/24Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms
    • A01N43/32Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms six-membered rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D495/00Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/12Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
    • C07D495/14Ortho-condensed systems

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Indole Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
  • Pyrrole Compounds (AREA)
  • Thiazole And Isothizaole Compounds (AREA)

Claims (4)

1. Fremgangsmåde til fremstilling af dithiin-tetracarboxy- diimider med den almene formel (I)
<D hvor R1 og R2 er ens eller forskellige og står for hydrogen, for Ci-Cs-alkyl, i givet fald substitueret en eller flere gange med halogen, -OR3, -COR4, for C3-C7-cycloalkyl, i givet fald substitueret en eller flere gange med halogen, Ci-C4_alkyl eller Ci-C4-halogenalkyl, for aryl eller aryl- (Ci-C4-alkyl) , hver især i givet fald substitueret en eller flere gange med halogen, Ci-C4-alkyl, Ci-C^-halogenalkyl, -COR4 eller sulfony1amino, R3 står for hydrogen, Ci-C4-alkyl, Ci-C4-alkylcarbonyl eller for aryl, i givet fald substitueret en eller flere gange med halogen, Ci-C4-akyl eller Ci-C4-halogenalkyl, R4 står for hydroxy, Ci-C4-alkyl eller Ci-C4~alkoxy, kendetegnet ved, at man omsætter (A) dichlormaleinsyreimider med formel (VI)
(VI) hvor R står for R1 eller R2, med et uorganisk sulfid eller hydrogensulfid i et opløsningsmiddel eller en opløsningsmiddelblanding i et molforhold mellem 0,2 og 0,95 mol af sulfid eller hydrogensulfid pr. mol dichlormaleinsyreimid med formel (VI) og opvarmer (B) reaktionsproduktet, som består af en blanding af forbindelser med formel (I) og polymere forbindelser med den almene formel (VII),
<VIT) hvor R uafhængigt af hinanden står for R1 eller R2, n står for et helt tal mellem 1 og 50, i et fortyndingsmiddel.
2. Fremgangsmåde ifølge krav 1, kendetegnet ved, at sulfidet eller hydrogensulfidet er udvalgt af gruppen bestående af lithiumsulfid, natriumsulfid, natriumhydrogensulfid, kaliumsulfid, calciumsulfid, calciumhydrogensulfid, magnesiumsulfid eller ammoniumsulfid eller blandinger af disse eller hydrater af disse.
3. Fremgangsmåde ifølge krav 1, kendetegnet ved, at opløsningsmidlet anvendes fra gruppen af amider, såsom formamid, N,N-dimethyl-formamid, N,N-dimethyl-acetamid, N-methyl-pyrrolidon; alkoholer såsom propanol, isobutanol, pentanol, ethylenglykol; estere såsom eddikesyremethylester, eddikesyreethylester, butylacetat; nitriler såsom acetonitril, butyronitril; ketoner såsom pinakolon, methyl-isobutylketon; dimethylsulfoxid eller sulfolan eller vand eller blandinger af disse.
4. Polymere forbindelser med formel (VII)
(Vil) hvor R uafhængigt af hinanden står for R1 eller R2, R1 og R2 er ens eller forskellige og står for hydrogen, for Ci-Cs-alkyl, i givet fald substitueret en eller flere gange med halogen, -OR3, -COR4, for C3-C7-cycloalkyl, i givet fald substitueret en eller flere gange med halogen, Ci-C4-akyl eller Ci-C4~halogenalkyl, for aryl eller aryl-(Ci-C4-alkyl), hver især i givet fald substitueret en eller flere gange med halogen, Ci-C^-alkyl, Ci-C^-halogenalkyl, -COR4 eller sulfonylamino, R3 står for hydrogen, Ci-C4-alkyl, Ci-C4-alkylcarbonyl eller for aryl, i givet fald substitueret en eller flere gange med halogen, Ci-C4-alkyl eller Ci-C4-halogenalkyl, R4 står for hydroxy, Ci-C4-alkyl eller Ci-C4-alkoxy, n står for et helt tal mellem 1 og 50.
DK11719280.7T 2010-05-21 2011-05-16 Fremgangsmåde til fremstilling af dithiin-tetracarboxy-diimider DK2571887T3 (da)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP10163519 2010-05-21
US34835510P 2010-05-26 2010-05-26
PCT/EP2011/057829 WO2011144550A1 (de) 2010-05-21 2011-05-16 Verfahren zur herstellung von dithiin-tetracarboxy-diimiden

Publications (1)

Publication Number Publication Date
DK2571887T3 true DK2571887T3 (da) 2014-11-24

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DK11719280.7T DK2571887T3 (da) 2010-05-21 2011-05-16 Fremgangsmåde til fremstilling af dithiin-tetracarboxy-diimider

Country Status (13)

Country Link
US (1) US8729275B2 (da)
EP (1) EP2571887B1 (da)
JP (1) JP5816268B2 (da)
KR (1) KR20130112719A (da)
CN (1) CN102939294B (da)
BR (1) BR112012029626A2 (da)
DK (1) DK2571887T3 (da)
ES (1) ES2518118T3 (da)
IL (1) IL223145A (da)
MX (1) MX2012013539A (da)
PL (1) PL2571887T3 (da)
RU (1) RU2574393C9 (da)
WO (1) WO2011144550A1 (da)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DK2558472T3 (da) * 2010-04-14 2014-10-27 Bayer Cropscience Ag Fremgangsmåde til fremstilling af dithiin-tetracarboxy-diimider
DK2558473T3 (da) 2010-04-14 2016-12-19 Bayer Ip Gmbh Fremgangsmåde til fremstilling af dithiin-tetracarboximider
EP2611814B1 (de) 2010-09-03 2014-09-24 Bayer Intellectual Property GmbH Verfahren zur herstellung von dithiin-tetracarboximiden
EP2641908A1 (de) * 2012-03-23 2013-09-25 Bayer CropScience AG Verfahren zur Herstellung von Dithiin-tetracarboximiden

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3364229A (en) * 1964-01-30 1968-01-16 Shell Oil Co 1, 4 dithiin-2, 3, 5, 6-tetracarboximides and process for their preparation
SU649292A3 (ru) * 1974-05-22 1979-02-25 Юниройял Инк Состав дл регулировани роста растений
US4067879A (en) * 1975-10-23 1978-01-10 E. I. Du Pont De Nemours And Company 1,4-Dithiino[2,3-c; 6,5-c']diisothiazole and related compounds
CA1150284A (en) * 1980-12-02 1983-07-19 Allan K.S. Tsai Method of making certain 2,3-dihydro-1,4-dithiins
PL143804B2 (en) 1985-10-15 1988-03-31 Univ Lodzki Process for preparing novel derivatives of 2,6-diphenyl-2,3,6,7-tetrahydro-1h,5h-1,4-dithiin-/2,3-c:5,6-c/-diprolo-1,3,5,7-tetraon substituted in phenyl ring
JP3530702B2 (ja) 1997-03-06 2004-05-24 京セラミタ株式会社 ジチオマレイン酸イミド誘導体を用いた電子写真感光体
CN100554251C (zh) * 2005-07-12 2009-10-28 中国科学院化学研究所 一种马来酰亚胺衍生物及其制备方法
US8865759B2 (en) 2008-10-15 2014-10-21 Bayer Intellectual Property Gmbh Use of dithiine-tetracarboximides for controlling phytopathogenic fungi

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Publication number Publication date
KR20130112719A (ko) 2013-10-14
PL2571887T3 (pl) 2015-01-30
CN102939294A (zh) 2013-02-20
IL223145A (en) 2016-05-31
US8729275B2 (en) 2014-05-20
EP2571887B1 (de) 2014-08-20
US20120022270A1 (en) 2012-01-26
BR112012029626A2 (pt) 2015-10-13
EP2571887A1 (de) 2013-03-27
MX2012013539A (es) 2013-01-24
RU2574393C2 (ru) 2016-02-10
CN102939294B (zh) 2015-09-02
RU2574393C9 (ru) 2016-10-10
RU2012155464A (ru) 2014-06-27
ES2518118T3 (es) 2014-11-04
JP5816268B2 (ja) 2015-11-18
IL223145A0 (en) 2013-02-03
JP2013527180A (ja) 2013-06-27
WO2011144550A1 (de) 2011-11-24

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