DD265315A5 - Fungizide und/oder bakterizide zusammensetzung - Google Patents

Fungizide und/oder bakterizide zusammensetzung Download PDF

Info

Publication number: DD265315A5
Authority: DD; German Democratic Republic
Prior art keywords: group; substituted; thiophene; cyano; compound
Prior art date: 1986-02-19

Application number

DD30001687A

Other languages

German (de)

English (en)

Inventor

Hendrik Dolman

Johannes Kuipers

Original Assignee

Duphar International Research,Nl

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.)

1986-02-19

Filing date

1987-02-18

Publication date

1989-03-01

1987-02-18 Application filed by Duphar International Research,Nl filed Critical Duphar International Research,Nl

1989-03-01 Publication of DD265315A5 publication Critical patent/DD265315A5/de

Links

239000000203 mixture Substances 0.000 title claims abstract description 65
239000000417 fungicide Substances 0.000 title description 3
239000003899 bactericide agent Substances 0.000 title description 2
150000001875 compounds Chemical class 0.000 claims abstract description 112
239000002689 soil Substances 0.000 claims abstract description 15
230000000855 fungicidal effect Effects 0.000 claims abstract description 8
239000004480 active ingredient Substances 0.000 claims abstract description 7
230000000844 anti-bacterial effect Effects 0.000 claims abstract description 6
-1 Ci-C 4 alkoxy Chemical group 0.000 claims description 45
125000004432 carbon atom Chemical group C* 0.000 claims description 26
239000013543 active substance Substances 0.000 claims description 20
229910052736 halogen Inorganic materials 0.000 claims description 15
125000000217 alkyl group Chemical group 0.000 claims description 14
125000005843 halogen group Chemical group 0.000 claims description 13
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 13
150000002367 halogens Chemical class 0.000 claims description 11
125000004093 cyano group Chemical group *C#N 0.000 claims description 10
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 9
239000007788 liquid Substances 0.000 claims description 9
125000003277 amino group Chemical group 0.000 claims description 8
125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 8
125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 8
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 8
125000001424 substituent group Chemical group 0.000 claims description 8
125000005842 heteroatom Chemical group 0.000 claims description 7
125000003545 alkoxy group Chemical group 0.000 claims description 6
125000004448 alkyl carbonyl group Chemical group 0.000 claims description 6
229910052717 sulfur Inorganic materials 0.000 claims description 6
125000005678 ethenylene group Chemical group [H]C([*:1])=C([H])[*:2] 0.000 claims description 5
244000005700 microbiome Species 0.000 claims description 5
239000007787 solid Substances 0.000 claims description 5
125000003118 aryl group Chemical group 0.000 claims description 4
125000004434 sulfur atom Chemical group 0.000 claims description 4
125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims description 3
125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 3
125000004414 alkyl thio group Chemical group 0.000 claims description 3
125000004104 aryloxy group Chemical group 0.000 claims description 3
125000000623 heterocyclic group Chemical group 0.000 claims description 3
125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 2
125000003342 alkenyl group Chemical group 0.000 claims description 2
125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 2
125000000304 alkynyl group Chemical group 0.000 claims description 2
125000005110 aryl thio group Chemical group 0.000 claims description 2
239000000463 material Substances 0.000 claims description 2
229910052760 oxygen Inorganic materials 0.000 claims description 2
125000004438 haloalkoxy group Chemical group 0.000 claims 1
125000001072 heteroaryl group Chemical group 0.000 claims 1
125000005553 heteroaryloxy group Chemical group 0.000 claims 1
125000005368 heteroarylthio group Chemical group 0.000 claims 1
241000233866 Fungi Species 0.000 abstract description 16
125000000446 sulfanediyl group Chemical group *S* 0.000 abstract description 6
241000894006 Bacteria Species 0.000 abstract description 4
244000053095 fungal pathogen Species 0.000 abstract description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 63
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238000002360 preparation method Methods 0.000 description 41
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238000006243 chemical reaction Methods 0.000 description 36
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238000000034 method Methods 0.000 description 25
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238000003756 stirring Methods 0.000 description 19
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IQIPNFOHABBEAP-UHFFFAOYSA-N 5-acetyl-2-methylsulfinylthiophene-3-carbonitrile Chemical compound CC(=O)C1=CC(C#N)=C(S(C)=O)S1 IQIPNFOHABBEAP-UHFFFAOYSA-N 0.000 description 16
229930192474 thiophene Natural products 0.000 description 16
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239000003495 polar organic solvent Substances 0.000 description 10
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239000000126 substance Substances 0.000 description 9
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IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
239000000460 chlorine Substances 0.000 description 8
KWYUFKZDYYNOTN-UHFFFAOYSA-M potassium hydroxide Inorganic materials [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 8
238000009835 boiling Methods 0.000 description 7
239000000543 intermediate Substances 0.000 description 7
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ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 6
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230000000694 effects Effects 0.000 description 6
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INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 6
HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 6
239000011734 sodium Substances 0.000 description 6
DKGYESBFCGKOJC-UHFFFAOYSA-N thiophen-3-amine Chemical compound NC=1C=CSC=1 DKGYESBFCGKOJC-UHFFFAOYSA-N 0.000 description 6
239000002253 acid Substances 0.000 description 5
229910052783 alkali metal Inorganic materials 0.000 description 5
239000002168 alkylating agent Substances 0.000 description 5
229940100198 alkylating agent Drugs 0.000 description 5
239000006185 dispersion Substances 0.000 description 5
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229910052708 sodium Inorganic materials 0.000 description 5
239000005995 Aluminium silicate Substances 0.000 description 4
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 4
229920003171 Poly (ethylene oxide) Polymers 0.000 description 4
SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 4
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KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 4
235000012211 aluminium silicate Nutrition 0.000 description 4
239000012876 carrier material Substances 0.000 description 4
238000012512 characterization method Methods 0.000 description 4
ORTQZVOHEJQUHG-UHFFFAOYSA-L copper(II) chloride Chemical compound Cl[Cu]Cl ORTQZVOHEJQUHG-UHFFFAOYSA-L 0.000 description 4
230000008020 evaporation Effects 0.000 description 4
239000008187 granular material Substances 0.000 description 4
239000005457 ice water Substances 0.000 description 4
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 4
238000002156 mixing Methods 0.000 description 4
229910052757 nitrogen Inorganic materials 0.000 description 4
239000007800 oxidant agent Substances 0.000 description 4
239000012312 sodium hydride Substances 0.000 description 4
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RMJMIRZCDLRLJI-UHFFFAOYSA-N 3-chloro-5-ethylsulfanylthiophene-2,4-dicarbonitrile Chemical compound CCSC=1SC(C#N)=C(Cl)C=1C#N RMJMIRZCDLRLJI-UHFFFAOYSA-N 0.000 description 3
125000000242 4-chlorobenzoyl group Chemical group ClC1=CC=C(C(=O)*)C=C1 0.000 description 3
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239000000600 sorbitol Substances 0.000 description 1
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239000004546 suspension concentrate Substances 0.000 description 1
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239000002641 tar oil Substances 0.000 description 1
MLGCXEBRWGEOQX-UHFFFAOYSA-N tetradifon Chemical compound C1=CC(Cl)=CC=C1S(=O)(=O)C1=CC(Cl)=C(Cl)C=C1Cl MLGCXEBRWGEOQX-UHFFFAOYSA-N 0.000 description 1
RAOIDOHSFRTOEL-UHFFFAOYSA-N tetrahydrothiophene Chemical compound C1CCSC1 RAOIDOHSFRTOEL-UHFFFAOYSA-N 0.000 description 1
WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 1
HERSKCAGZCXYMC-UHFFFAOYSA-N thiophen-3-ol Chemical compound OC=1C=CSC=1 HERSKCAGZCXYMC-UHFFFAOYSA-N 0.000 description 1
IZXOWBGBNVBNRE-UHFFFAOYSA-N thiophene-2,4-dicarbonitrile Chemical class N#CC1=CSC(C#N)=C1 IZXOWBGBNVBNRE-UHFFFAOYSA-N 0.000 description 1
RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 description 1
NFACJZMKEDPNKN-UHFFFAOYSA-N trichlorfon Chemical compound COP(=O)(OC)C(O)C(Cl)(Cl)Cl NFACJZMKEDPNKN-UHFFFAOYSA-N 0.000 description 1
FIDXVVHZWRFINX-UHFFFAOYSA-N tris(2-methyl-2-phenylpropyl)tin Chemical compound C=1C=CC=CC=1C(C)(C)C[Sn](CC(C)(C)C=1C=CC=CC=1)CC(C)(C)C1=CC=CC=C1 FIDXVVHZWRFINX-UHFFFAOYSA-N 0.000 description 1
238000005406 washing Methods 0.000 description 1
239000008096 xylene Substances 0.000 description 1
229940089401 xylon Drugs 0.000 description 1
239000012138 yeast extract Substances 0.000 description 1
AMHNZOICSMBGDH-UHFFFAOYSA-L zineb Chemical compound [Zn+2].[S-]C(=S)NCCNC([S-])=S AMHNZOICSMBGDH-UHFFFAOYSA-L 0.000 description 1

Landscapes

Agricultural Chemicals And Associated Chemicals (AREA)
Plural Heterocyclic Compounds (AREA)
Heterocyclic Compounds Containing Sulfur Atoms (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

DD30001687A 1986-02-19 1987-02-18 Fungizide und/oder bakterizide zusammensetzung DD265315A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
NL8600416		1986-02-19

Publications (1)

Publication Number	Publication Date
DD265315A5 true DD265315A5 (de)	1989-03-01

Family

ID=19847598

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD30001687A DD265315A5 (de)	1986-02-19	1987-02-18	Fungizide und/oder bakterizide zusammensetzung

Country Status (5)

Country	Link
JP (1)	JPS62192353A (cs)
CS (1)	CS268823B2 (cs)
DD (1)	DD265315A5 (cs)
SU (1)	SU1496633A3 (cs)
ZA (1)	ZA871109B (cs)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE19503136A1 (de) *	1995-02-01	1996-08-08	Hoechst Ag	Substituierte Thiophenylsulfonylharnstoffe und -thioharnstoffe, Verfahren zu ihrer Herstellung, ihre Verwendung als Medikament oder Diagnostikum sowie sie enthaltendes Medikament
JP4975738B2 (ja) *	2006-04-17	2012-07-11	三井化学アグロ株式会社	２−アルケニル−３−アミノチオフェン誘導体及びその製造方法

1987
- 1987-02-16 SU SU874028996A patent/SU1496633A3/ru active
- 1987-02-16 ZA ZA871109A patent/ZA871109B/xx unknown
- 1987-02-17 CS CS871037A patent/CS268823B2/cs unknown
- 1987-02-18 DD DD30001687A patent/DD265315A5/de not_active IP Right Cessation
- 1987-02-19 JP JP3685787A patent/JPS62192353A/ja active Pending

Also Published As

Publication number	Publication date
JPS62192353A (ja)	1987-08-22
SU1496633A3 (ru)	1989-07-23
CS268823B2 (en)	1990-04-11
CS103787A2 (en)	1989-09-12
ZA871109B (en)	1987-10-28

Legal Events

Date	Code	Title	Description
1996-01-18	ENJ	Ceased due to non-payment of renewal fee

Publication	Publication Date	Title
DE3881443T2 (de)	1993-11-25	Imidazol-Verbindung und diese enthaltende biozide Zusammensetzungen.
DE2804299C2 (cs)	1987-10-29
EP0007990A1 (de)	1980-02-20	Pyrazolätherderivate, Verfahren zu ihrer Herstellung und Herbizide, die diese Verbindungen enthalten
DE2250077C2 (de)	1984-04-26	Pflanzenschutzmittel auf Basis eines s-Triazolo[3,4-b]benzoxazols oder s-Triazolo[3,4-b]benzthiazols und neue s-Triazolo[3,4-b]benzthiazole
DE3713774C2 (de)	1993-10-07	Pyrazol-Derivate, Verfahren zu ihrer Herstellung und diese enthaltende Fungizide
DD155384A5 (de)	1982-06-09	Fungizide und/oder bakterizide zusammensetzungen
DE3123018C2 (de)	1984-06-20	Substituierte Cyclohexan-1,3-dion-Derivate, Verfahren zu deren Herstellung und herbicide Mittel
DE3852587T2 (de)	1995-05-18	Pyridazinon-Derivate und Zusammenstellungen zum kontrollieren und/oder Verhindern der Insektenplage.
EP0226536A2 (de)	1987-06-24	(Di)alkoxycarbonyl-amino-s-triazin-Derivate gegen tier- und pflanzenparasitäre Schädlinge
DE69110749T2 (de)	1995-11-16	Barbitursäurederivate mit insektizider Wirkung.
EP0368212B1 (de)	1995-09-20	Herbizide Mittel, die 2-(4-Heteroaryloxy)- oder 2-(4-Aryloxy)-phenoxy-essig- oder -propionsäurederivate und/oder Cyclohexenonderivate als herbizide Wirkstoffe und Naphthalinderivate als Antidots enthalten, sowie ihre Verwendung zur Bekämpfung unerwünschten Pflanzenwuchses
DE2619303A1 (de)	1976-11-18	Neue schwefelhaltige bisformamidine, verfahren zu ihrer herstellung und verwendung derselben sowie diese enthaltende land-, garten- und forstwirtschaftliche chemikalien
DE2123277A1 (de)	1971-12-02	Insektizide Mittel
DE60108209T2 (de)	2005-12-29	Fungizide Phenylimidatderivate
DD202090A5 (de)	1983-08-31	Herbizides mittel
DE3872634T2 (de)	1992-12-03	Thiadiazine, verfahren zu deren herstellung und insektizide.
DE2902832A1 (de)	1979-08-02	Mikrobizide mittel
DE4011740A1 (de)	1990-10-18	1,2,4-triazinonderivate
DE1670709A1 (de)	1970-12-03	Pestizide Mittel
EP0391849B1 (de)	1995-04-19	Pyridyl-methylenamino-1,2,4-triazinone
DE2557406A1 (de)	1976-07-08	Neue thioharnstoffverbindungen, verfahren zu ihrer herstellung und ihre verwendung als fungizide
DD293952A5 (de)	1991-09-19	5-substituierte 3-arylisoxazol-derivate, deren herstellung und ihre verwendung als schaedlingsbekaempfungsmittel, insbesondere gegen nematoden
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