DK169743B1 - Thiazolderivater fremgangsmåde til fremstilling deraf,fungicid præparat, fremgangsmåde til bekæmpelse af svampe og anvendelse som fungicid til behandling af planter - Google Patents

Thiazolderivater fremgangsmåde til fremstilling deraf,fungicid præparat, fremgangsmåde til bekæmpelse af svampe og anvendelse som fungicid til behandling af planter Download PDF

Info

Publication number: DK169743B1
Authority: DK; Denmark
Prior art keywords: group; compound; formula; plants; atom
Prior art date: 1987-06-25

Application number

DK346788A

Other languages

Danish (da)

English (en)

Other versions

DK346788D0 (da

DK346788A (da

Inventor

John Robert Howe Wilson

Ernest Haddock

Original Assignee

Shell Int Research

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.)

1987-06-25

Filing date

1988-06-23

Publication date

1995-02-13

1988-06-23 Application filed by Shell Int Research filed Critical Shell Int Research

1988-06-23 Publication of DK346788D0 publication Critical patent/DK346788D0/da

1988-12-26 Publication of DK346788A publication Critical patent/DK346788A/da

1995-02-13 Application granted granted Critical

1995-02-13 Publication of DK169743B1 publication Critical patent/DK169743B1/da

Links

238000000034 method Methods 0.000 title claims abstract description 19
238000002360 preparation method Methods 0.000 title claims abstract description 17
239000000417 fungicide Substances 0.000 title claims abstract description 11
230000000855 fungicidal effect Effects 0.000 title claims description 18
150000007979 thiazole derivatives Chemical class 0.000 title abstract description 3
150000001875 compounds Chemical class 0.000 claims abstract description 88
-1 cyano, nitro, amino Chemical group 0.000 claims abstract description 32
239000000203 mixture Substances 0.000 claims abstract description 28
150000003839 salts Chemical class 0.000 claims abstract description 19
229910052751 metal Chemical class 0.000 claims abstract description 10
239000002184 metal Chemical class 0.000 claims abstract description 10
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 7
229910052760 oxygen Inorganic materials 0.000 claims abstract description 6
239000001301 oxygen Substances 0.000 claims abstract description 6
125000003545 alkoxy group Chemical group 0.000 claims abstract description 5
125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 5
125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 4
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 3
YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical group C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims abstract description 3
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims abstract description 3
239000001257 hydrogen Substances 0.000 claims abstract description 3
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 3
239000004480 active ingredient Substances 0.000 claims description 11
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239000002253 acid Substances 0.000 claims description 10
239000004094 surface-active agent Substances 0.000 claims description 10
239000000460 chlorine Substances 0.000 claims description 8
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 7
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101150009274 nhr-1 gene Proteins 0.000 claims description 6
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KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims description 5
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125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 2
125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
125000004430 oxygen atom Chemical group O* 0.000 claims description 2
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NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract description 3
125000005843 halogen group Chemical group 0.000 abstract description 2
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238000002474 experimental method Methods 0.000 description 9
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WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 8
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CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 7
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HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 6
MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 6
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239000002585 base Substances 0.000 description 6
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UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 6
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YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 4
YZVFSQQHQPPKNX-UHFFFAOYSA-N 1,3-thiazole-5-carboxylic acid Chemical compound OC(=O)C1=CN=CS1 YZVFSQQHQPPKNX-UHFFFAOYSA-N 0.000 description 3
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SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
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239000005909 Kieselgur Substances 0.000 description 1
238000005677 Lawesson carbonylation reaction Methods 0.000 description 1
NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
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UIQWBVPFHHQZHH-UHFFFAOYSA-N OOOOOOOOOOOOOO Chemical compound OOOOOOOOOOOOOO UIQWBVPFHHQZHH-UHFFFAOYSA-N 0.000 description 1
241000736122 Parastagonospora nodorum Species 0.000 description 1
CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 1
241001123569 Puccinia recondita Species 0.000 description 1
206010037888 Rash pustular Diseases 0.000 description 1
RRTCJVBFMMTZSS-UHFFFAOYSA-N SSSSSSSSSSSSS Chemical compound SSSSSSSSSSSSS RRTCJVBFMMTZSS-UHFFFAOYSA-N 0.000 description 1
DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
229920002125 Sokalan® Polymers 0.000 description 1
244000061456 Solanum tuberosum Species 0.000 description 1
235000002595 Solanum tuberosum Nutrition 0.000 description 1
CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
229930006000 Sucrose Natural products 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
241000219094 Vitaceae Species 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
239000000443 aerosol Substances 0.000 description 1
238000005054 agglomeration Methods 0.000 description 1
230000002776 aggregation Effects 0.000 description 1
239000003513 alkali Substances 0.000 description 1
SNAAJJQQZSMGQD-UHFFFAOYSA-N aluminum magnesium Chemical compound [Mg].[Al] SNAAJJQQZSMGQD-UHFFFAOYSA-N 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
239000000908 ammonium hydroxide Substances 0.000 description 1
BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
229910052921 ammonium sulfate Inorganic materials 0.000 description 1
235000011130 ammonium sulphate Nutrition 0.000 description 1
229960003116 amyl nitrite Drugs 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
230000002528 anti-freeze Effects 0.000 description 1
239000002518 antifoaming agent Substances 0.000 description 1
150000001491 aromatic compounds Chemical class 0.000 description 1
239000010426 asphalt Substances 0.000 description 1
235000013871 bee wax Nutrition 0.000 description 1
239000012166 beeswax Substances 0.000 description 1
238000009835 boiling Methods 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
159000000007 calcium salts Chemical class 0.000 description 1
YYRMJZQKEFZXMX-UHFFFAOYSA-N calcium;phosphoric acid Chemical class [Ca+2].OP(O)(O)=O.OP(O)(O)=O YYRMJZQKEFZXMX-UHFFFAOYSA-N 0.000 description 1
239000004359 castor oil Substances 0.000 description 1
235000019438 castor oil Nutrition 0.000 description 1
235000013339 cereals Nutrition 0.000 description 1
150000001793 charged compounds Chemical class 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
239000003638 chemical reducing agent Substances 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
239000012320 chlorinating reagent Substances 0.000 description 1
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238000004440 column chromatography Methods 0.000 description 1
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230000001419 dependent effect Effects 0.000 description 1
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238000003113 dilution method Methods 0.000 description 1
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125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
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239000003337 fertilizer Substances 0.000 description 1
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230000009969 flowable effect Effects 0.000 description 1
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
235000021021 grapes Nutrition 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
230000002363 herbicidal effect Effects 0.000 description 1
GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
230000003301 hydrolyzing effect Effects 0.000 description 1
238000005470 impregnation Methods 0.000 description 1
238000011065 in-situ storage Methods 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
230000000749 insecticidal effect Effects 0.000 description 1
239000012948 isocyanate Substances 0.000 description 1
150000002513 isocyanates Chemical class 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
125000005647 linker group Chemical group 0.000 description 1
239000012263 liquid product Substances 0.000 description 1
239000000391 magnesium silicate Substances 0.000 description 1
235000012243 magnesium silicates Nutrition 0.000 description 1
238000001819 mass spectrum Methods 0.000 description 1
239000002609 medium Substances 0.000 description 1
UJNNCGWBDJHCEM-UHFFFAOYSA-N methyl 2-amino-1,3-thiazole-5-carboxylate Chemical compound COC(=O)C1=CN=C(N)S1 UJNNCGWBDJHCEM-UHFFFAOYSA-N 0.000 description 1
239000010445 mica Substances 0.000 description 1
229910052618 mica group Inorganic materials 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
239000012184 mineral wax Substances 0.000 description 1
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229910052901 montmorillonite Inorganic materials 0.000 description 1
210000003097 mucus Anatomy 0.000 description 1
CSDTZUBPSYWZDX-UHFFFAOYSA-N n-pentyl nitrite Chemical compound CCCCCON=O CSDTZUBPSYWZDX-UHFFFAOYSA-N 0.000 description 1
239000000025 natural resin Substances 0.000 description 1
208000013435 necrotic lesion Diseases 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
230000000149 penetrating effect Effects 0.000 description 1
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
239000004800 polyvinyl chloride Substances 0.000 description 1
229920000915 polyvinyl chloride Polymers 0.000 description 1
235000014483 powder concentrate Nutrition 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
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208000029561 pustule Diseases 0.000 description 1
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239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
238000004062 sedimentation Methods 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
235000019333 sodium laurylsulphate Nutrition 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
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238000003756 stirring Methods 0.000 description 1
238000003860 storage Methods 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
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125000001273 sulfonato group Chemical class [O-]S(*)(=O)=O 0.000 description 1
150000003459 sulfonic acid esters Chemical class 0.000 description 1
150000003460 sulfonic acids Chemical class 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
239000002426 superphosphate Substances 0.000 description 1
239000000375 suspending agent Substances 0.000 description 1
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239000011701 zinc Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/22—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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 ring carbon atoms
- C07D277/56—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles

Landscapes

Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
Environmental Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Plant Pathology (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Thiazole And Isothizaole Compounds (AREA)
Saccharide Compounds (AREA)
Steroid Compounds (AREA)
Plural Heterocyclic Compounds (AREA)

DK346788A 1987-06-25 1988-06-23 Thiazolderivater fremgangsmåde til fremstilling deraf,fungicid præparat, fremgangsmåde til bekæmpelse af svampe og anvendelse som fungicid til behandling af planter DK169743B1 (da)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
GB8714920		1987-06-25
GB878714920A GB8714920D0 (en)	1987-06-25	1987-06-25	Thiazole derivatives

Publications (3)

Publication Number	Publication Date
DK346788D0 DK346788D0 (da)	1988-06-23
DK346788A DK346788A (da)	1988-12-26
DK169743B1 true DK169743B1 (da)	1995-02-13

Family

ID=10619553

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DK346788A DK169743B1 (da)	1987-06-25	1988-06-23	Thiazolderivater fremgangsmåde til fremstilling deraf,fungicid præparat, fremgangsmåde til bekæmpelse af svampe og anvendelse som fungicid til behandling af planter

Country Status (13)

Country	Link
US (1)	US4877802A (fr)
EP (1)	EP0296673B1 (fr)
JP (1)	JPS6426572A (fr)
KR (1)	KR890000449A (fr)
CN (1)	CN1022015C (fr)
AT (1)	ATE102611T1 (fr)
AU (1)	AU615658B2 (fr)
CA (1)	CA1328867C (fr)
DE (1)	DE3888245T2 (fr)
DK (1)	DK169743B1 (fr)
ES (1)	ES2061628T3 (fr)
GB (1)	GB8714920D0 (fr)
SU (1)	SU1579458A3 (fr)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3805058A1 (de) *	1988-02-18	1989-08-31	Bayer Ag	N-sulfenylierte 2-amino-4-chlor-thiazol-sulfonamide, ihre verwendung, verfahren zu ihrer herstellung und die dabei auftretenden zwischenprodukte 2,4-dichlor-thiazol-sulfonsaeurechlorid und 2-amino-4-chlor-thiazol-sulfonsaeureamid
US5264448A (en) *	1989-04-19	1993-11-23	Sumitomo Chemical Company, Limited	Amide compound and its production and use
GB8909737D0 (en) *	1989-04-27	1989-06-14	Shell Int Research	Thiazole derivatives
CA2014880A1 (fr) *	1989-04-27	1990-10-27	Indu Sawhney	Derives du thiazole
HU207702B (en) *	1989-06-21	1993-05-28	Makhteshim Chem Works Ltd	Process for producing n-/n-propyl/-n/2-/2,4,6-trichloro-phenoxy/-ethyl/-amine
IL90703A (en) *	1989-06-21	1994-10-07	Makhteshim Chem Works Ltd	Method of preparing n-n-propyl-n-2-(2,4,6-trichlorophenoxy)-ethyl amine
IL90704A (en) *	1989-06-21	1994-10-07	Makhteshim Chem Works Ltd	Method for the preparation of N-N-) 2,4,6-trichlorophenoxy (environmentally reliable ethylene)
IL103614A (en) *	1991-11-22	1998-09-24	Basf Ag	Carboxamides for controlling botrytis and certain novel such compounds
US5514643A (en) *	1993-08-16	1996-05-07	Lucky Ltd.	2-aminothiazolecarboxamide derivatives, processes for preparing the same and use thereof for controlling phytopathogenic organisms
US6001855A (en) *	1998-01-02	1999-12-14	Hoffman-La Roche Inc.	Thiazole derivatives
CN1065859C (zh) *	1998-08-27	2001-05-16	江苏辉丰农化股份有限公司	制备用作农药中间体的苯氧基醚的新方法
CN100357283C (zh) *	2002-04-02	2007-12-26	中国科学院上海药物研究所	一类甲硫氨酰氨肽酶抑制剂
WO2006110626A1 (fr) *	2005-04-12	2006-10-19	Merck & Co., Inc.	Antagonistes du récepteur de l’orexine de type amidopropoxyphényle
EP1792901A1 (fr)	2005-11-22	2007-06-06	Bayer CropScience S.A.	Derives de n-(1-alkyl-2-phenylethyl)-carboxamide et leur utilisation en tant que fongicide
EP1787981A1 (fr)	2005-11-22	2007-05-23	Bayer CropScience S.A.	Nouveaux dörivés de N-phénéthyl carboxamide
CN101778827B (zh) *	2007-07-26	2012-10-10	先正达参股股份有限公司	杀微生物剂
CN103130740A (zh) *	2011-11-29	2013-06-05	长江大学	拌种灵的氨基酸衍生物及其作为杀菌剂的用途
CN114380767A (zh) *	2022-01-19	2022-04-22	安徽理工大学	一种含二苯胺基的噻唑酰胺类化合物及其制备方法与应用

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3709992A (en) *	1966-12-07	1973-01-09	Us Rubber Co	Fungicidal use of certain carboxamidothiazoles
US3725427A (en) *	1966-12-07	1973-04-03	Uniroyal Ltd	Certain 2,4-dimethyl-5-carboxamido-thiazoles
US3856806A (en) *	1973-03-07	1974-12-24	Pfizer	Thiazolecarboxamide sulfonylurea hypoglycemic agents
DE2320387A1 (de) *	1973-04-21	1974-10-31	Boehringer Mannheim Gmbh	Phenoxyalkylcarbonsaeurederivate und verfahren zur herstellung derselben
FR2336131A2 (fr) *	1975-02-28	1977-07-22	Roussel Uclaf	Nouveaux derives de n-hydroxy thiazole 5-carboxamide, leur procede de preparation et leur application comme medicaments
DE3120804A1 (de) *	1981-05-25	1982-12-16	Basf Ag, 6700 Ludwigshafen	N-substituierte 2-methylnaphthylamide, verfahren zu ihrer herstellung und ihre verwendung zur bekaempfung von pilzen
DE3133418A1 (de) *	1981-08-24	1983-03-10	Basf Ag, 6700 Ludwigshafen	Thiazolyl- und isothiazolylcarbonsaeureanilide, verfahren zu ihrer herstellung und ihre verwendung als fungizide

1987
- 1987-06-25 GB GB878714920A patent/GB8714920D0/en active Pending
1988
- 1988-05-27 US US07/199,430 patent/US4877802A/en not_active Expired - Fee Related
- 1988-06-01 CA CA000568279A patent/CA1328867C/fr not_active Expired - Fee Related
- 1988-06-15 AT AT88201227T patent/ATE102611T1/de not_active IP Right Cessation
- 1988-06-15 DE DE3888245T patent/DE3888245T2/de not_active Expired - Fee Related
- 1988-06-15 ES ES88201227T patent/ES2061628T3/es not_active Expired - Lifetime
- 1988-06-15 EP EP88201227A patent/EP0296673B1/fr not_active Expired - Lifetime
- 1988-06-23 DK DK346788A patent/DK169743B1/da not_active IP Right Cessation
- 1988-06-23 JP JP63153706A patent/JPS6426572A/ja active Pending
- 1988-06-23 AU AU18329/88A patent/AU615658B2/en not_active Ceased
- 1988-06-23 SU SU884355953A patent/SU1579458A3/ru active
- 1988-06-23 KR KR1019880007616A patent/KR890000449A/ko not_active Ceased
- 1988-06-23 CN CN88103766A patent/CN1022015C/zh not_active Expired - Fee Related

Also Published As

Publication number	Publication date
EP0296673B1 (fr)	1994-03-09
DK346788D0 (da)	1988-06-23
CN1033626A (zh)	1989-07-05
DK346788A (da)	1988-12-26
GB8714920D0 (en)	1987-07-29
ES2061628T3 (es)	1994-12-16
SU1579458A3 (ru)	1990-07-15
JPS6426572A (en)	1989-01-27
AU615658B2 (en)	1991-10-10
CA1328867C (fr)	1994-04-26
DE3888245D1 (de)	1994-04-14
US4877802A (en)	1989-10-31
DE3888245T2 (de)	1994-06-16
CN1022015C (zh)	1993-09-08
EP0296673A1 (fr)	1988-12-28
KR890000449A (ko)	1989-03-14
AU1832988A (en)	1989-01-05
ATE102611T1 (de)	1994-03-15

Legal Events

Date	Code	Title	Description
1995-02-13	B1	Patent granted (law 1993)
1998-02-16	PBP	Patent lapsed

Publication	Publication Date	Title
DK169743B1 (da)	1995-02-13	Thiazolderivater fremgangsmåde til fremstilling deraf,fungicid præparat, fremgangsmåde til bekæmpelse af svampe og anvendelse som fungicid til behandling af planter
CA1338418C (fr)	1996-06-25	Composition microbicide a base de derives de l'acide 2-chloro-4-trifluoromethylthiazolyl-5-carboxylique
EP0395175B1 (fr)	1994-09-07	Dérivés du thiazole
JPS6348866B2 (fr)	1988-09-30
AU612573B2 (en)	1991-07-18	Benzothiazinone derivatives
RU2066320C1 (ru)	1996-09-10	Производные тиазола, способ их получения и способ борьбы с грибками
DK165636B (da)	1992-12-28	1,5-disubstituerede imidazolderivater, fremgangsmaade til fremstilling af saadanne forbindelser, fungicidt praeparat indeholdende saadanne forbindelser samt anvendelse af saadanne forbindelser som fungicider
CS266558B2 (en)	1990-01-12	Fungicide and method of its efficient substance production
CS270213B2 (en)	1990-06-13	Fungicide and method of its active substance production
JPH0130822B2 (fr)	1989-06-22
US5332753A (en)	1994-07-26	Thiazole derivatives, their preparation and their use as fungicides
HU206021B (en)	1992-08-28	Fungicidal compositions comprising substituted pyridine derivatives as active ingredient and process for producing the active ingredients
KR940011459B1 (ko)	1994-12-15	티아지논 유도체의 제조 방법
US4404213A (en)	1983-09-13	Derivatives of certain pyridyliminomethyl-benzenes
EP0091148B1 (fr)	1987-11-19	Composés hétérocycliques fongicides
EP0152131B1 (fr)	1989-08-23	Dérivés de carboxamide, leur préparation et leur utilisation comme fongicides
HU206022B (en)	1992-08-28	Fungicidal composition comprising imidazole derivative as active ingredient, process for producing the active ingredient and for applying the composition
CZ28896A3 (en)	1996-08-14	£1,2,4\|thiazoles, process of their preparation, herbicidal agent based thereon and method of suppressing growth of plants
EP0319057B1 (fr)	1994-03-02	Dérivés d'imidazole
US4355035A (en)	1982-10-19	Derivatives of certain pyridyliminomethylbenzenes
US4927841A (en)	1990-05-22	Fungicidal imidazole oxime derivatives
GB2182327A (en)	1987-05-13	Imidazoles, their preparation and their use as fungicides
GB2139213A (en)	1984-11-07	Heterocyclic amido derivatives
EP0535227A1 (fr)	1993-04-07	Derive d'amidine heterocyclique n-substitue