DD239516A5 - Acylierte saccharin-derivate - Google Patents

Acylierte saccharin-derivate Download PDF

Info

Publication number: DD239516A5
Authority: DD; German Democratic Republic
Prior art keywords: alkyl; formula; saccharin; acylated; phenyl
Prior art date: 1984-09-12

Application number

DD85280522A

Other languages

German (de)

English (en)

Inventor

Herbert Salzburg

Manfred Hajek

Hermann Hagemann

Engelbert Kuehle

Wolfgang Fuehrer

Gerd Haenssler

Wilhelm Brandes

Paul Reinecke

Original Assignee

��@��k��

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.)

1984-09-12

Filing date

1985-09-11

Publication date

1986-10-01

1985-09-11 Application filed by ��@��k�� filed Critical ��@��k��

1986-10-01 Publication of DD239516A5 publication Critical patent/DD239516A5/de

Links

CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical class C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 title claims description 27
125000000217 alkyl group Chemical group 0.000 claims abstract description 22
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 14
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 8
239000001301 oxygen Substances 0.000 claims abstract description 8
229910052760 oxygen Inorganic materials 0.000 claims abstract description 8
125000003545 alkoxy group Chemical group 0.000 claims abstract description 7
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 6
125000004414 alkyl thio group Chemical group 0.000 claims abstract description 6
125000004438 haloalkoxy group Chemical group 0.000 claims abstract description 6
125000001188 haloalkyl group Chemical group 0.000 claims abstract description 6
125000006678 phenoxycarbonyl group Chemical group 0.000 claims abstract description 6
125000004453 alkoxycarbonyl group Chemical group 0.000 claims abstract description 5
125000005110 aryl thio group Chemical group 0.000 claims abstract description 5
125000004104 aryloxy group Chemical group 0.000 claims abstract description 5
125000000000 cycloalkoxy group Chemical group 0.000 claims abstract description 5
125000003107 substituted aryl group Chemical group 0.000 claims abstract description 5
238000002360 preparation method Methods 0.000 claims description 15
239000000203 mixture Substances 0.000 claims description 11
238000000034 method Methods 0.000 claims description 9
241000607479 Yersinia pestis Species 0.000 claims description 6
229910052757 nitrogen Inorganic materials 0.000 claims description 6
239000000575 pesticide Substances 0.000 claims description 6
125000004433 nitrogen atom Chemical group N* 0.000 claims description 5
229910052717 sulfur Chemical group 0.000 claims description 5
239000011593 sulfur Chemical group 0.000 claims description 5
239000004606 Fillers/Extenders Substances 0.000 claims description 4
125000004995 haloalkylthio group Chemical group 0.000 claims description 3
239000004094 surface-active agent Substances 0.000 claims description 3
241000894006 Bacteria Species 0.000 claims description 2
241000233866 Fungi Species 0.000 claims description 2
238000002156 mixing Methods 0.000 claims description 2
230000000361 pesticidal effect Effects 0.000 claims 1
-1 halogenoalkylthio Chemical group 0.000 abstract description 17
235000019204 saccharin Nutrition 0.000 abstract description 12
229940081974 saccharin Drugs 0.000 abstract description 11
239000000901 saccharin and its Na,K and Ca salt Substances 0.000 abstract description 11
239000005864 Sulphur Chemical group 0.000 abstract 1
150000001875 compounds Chemical class 0.000 description 35
125000004432 carbon atom Chemical group C* 0.000 description 19
241000196324 Embryophyta Species 0.000 description 17
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 13
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 13
239000002904 solvent Substances 0.000 description 13
239000004480 active ingredient Substances 0.000 description 11
239000003995 emulsifying agent Substances 0.000 description 10
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
201000010099 disease Diseases 0.000 description 7
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 7
238000009472 formulation Methods 0.000 description 7
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
239000003921 oil Substances 0.000 description 6
235000019198 oils Nutrition 0.000 description 6
230000001681 protective effect Effects 0.000 description 6
239000000725 suspension Substances 0.000 description 6
IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 5
240000007594 Oryza sativa Species 0.000 description 5
125000002877 alkyl aryl group Chemical group 0.000 description 5
239000000460 chlorine Substances 0.000 description 5
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 5
238000011156 evaluation Methods 0.000 description 5
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125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
239000002689 soil Substances 0.000 description 4
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
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PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 3
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235000007164 Oryza sativa Nutrition 0.000 description 3
241000736122 Parastagonospora nodorum Species 0.000 description 3
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150000002170 ethers Chemical class 0.000 description 3
239000011737 fluorine Substances 0.000 description 3
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VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
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RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 2
ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 2
XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 2
241000588698 Erwinia Species 0.000 description 2
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
241000223194 Fusarium culmorum Species 0.000 description 2
206010061217 Infestation Diseases 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical class [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
235000007688 Lycopersicon esculentum Nutrition 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
241000233614 Phytophthora Species 0.000 description 2
229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
241000228453 Pyrenophora Species 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
240000003768 Solanum lycopersicum Species 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
230000000844 anti-bacterial effect Effects 0.000 description 2
125000003118 aryl group Chemical group 0.000 description 2
125000001309 chloro group Chemical group Cl* 0.000 description 2
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
239000012973 diazabicyclooctane Substances 0.000 description 2
231100000676 disease causative agent Toxicity 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
239000000975 dye Substances 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 description 2
FKRCODPIKNYEAC-UHFFFAOYSA-N ethyl propionate Chemical compound CCOC(=O)CC FKRCODPIKNYEAC-UHFFFAOYSA-N 0.000 description 2
239000000417 fungicide Substances 0.000 description 2
150000008282 halocarbons Chemical class 0.000 description 2
238000011534 incubation Methods 0.000 description 2
IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate Chemical compound [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 2
239000012948 isocyanate Substances 0.000 description 2
NONOKGVFTBWRLD-UHFFFAOYSA-N isocyanatosulfanylimino(oxo)methane Chemical class O=C=NSN=C=O NONOKGVFTBWRLD-UHFFFAOYSA-N 0.000 description 2
150000002576 ketones Chemical class 0.000 description 2
238000002844 melting Methods 0.000 description 2
230000008018 melting Effects 0.000 description 2
125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 2
239000011707 mineral Substances 0.000 description 2
239000003208 petroleum Substances 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
239000000243 solution Substances 0.000 description 2
241000894007 species Species 0.000 description 2
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
239000008096 xylene Substances 0.000 description 2
229910052725 zinc Inorganic materials 0.000 description 2
WISFMUWARKMDLQ-UHFFFAOYSA-N 1,1,3-trioxo-n-phenyl-1,2-benzothiazole-2-carboxamide Chemical class O=C1C2=CC=CC=C2S(=O)(=O)N1C(=O)NC1=CC=CC=C1 WISFMUWARKMDLQ-UHFFFAOYSA-N 0.000 description 1
DLOXXNDEZOGZQW-UHFFFAOYSA-N 1,1-dimethyl-3-(oxomethylidene)urea Chemical compound CN(C)C(=O)N=C=O DLOXXNDEZOGZQW-UHFFFAOYSA-N 0.000 description 1
KAYCUAMUHSXVRJ-UHFFFAOYSA-N 1-butyl-3-(oxomethylidene)-1-phenylurea Chemical compound CCCCN(C(=O)N=C=O)C1=CC=CC=C1 KAYCUAMUHSXVRJ-UHFFFAOYSA-N 0.000 description 1
244000215068 Acacia senegal Species 0.000 description 1
RGCKGOZRHPZPFP-UHFFFAOYSA-N Alizarin Natural products C1=CC=C2C(=O)C3=C(O)C(O)=CC=C3C(=O)C2=C1 RGCKGOZRHPZPFP-UHFFFAOYSA-N 0.000 description 1
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IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
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UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 1
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229910052742 iron Inorganic materials 0.000 description 1
150000002513 isocyanates Chemical class 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
239000000787 lecithin Substances 0.000 description 1
235000010445 lecithin Nutrition 0.000 description 1
WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical class [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000004579 marble Substances 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
YOVQDZPAVARTTR-UHFFFAOYSA-N methyl n-(oxomethylidene)carbamate Chemical compound COC(=O)N=C=O YOVQDZPAVARTTR-UHFFFAOYSA-N 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
230000003641 microbiacidal effect Effects 0.000 description 1
244000005700 microbiome Species 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
229910052750 molybdenum Inorganic materials 0.000 description 1
239000011733 molybdenum Substances 0.000 description 1
229910052901 montmorillonite Inorganic materials 0.000 description 1
WHQSYGRFZMUQGQ-UHFFFAOYSA-N n,n-dimethylformamide;hydrate Chemical compound O.CN(C)C=O WHQSYGRFZMUQGQ-UHFFFAOYSA-N 0.000 description 1
GINQYTLDMNFGQP-UHFFFAOYSA-N n,n-dimethylformamide;methylsulfinylmethane Chemical compound CS(C)=O.CN(C)C=O GINQYTLDMNFGQP-UHFFFAOYSA-N 0.000 description 1
IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
229940042880 natural phospholipid Drugs 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
235000015097 nutrients Nutrition 0.000 description 1
235000013348 organic food Nutrition 0.000 description 1
239000011368 organic material Substances 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
229910052625 palygorskite Inorganic materials 0.000 description 1
239000006072 paste Substances 0.000 description 1
244000052769 pathogen Species 0.000 description 1
125000000951 phenoxy group Chemical class [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
150000003904 phospholipids Chemical class 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
WHHIPMZEDGBUCC-UHFFFAOYSA-N probenazole Chemical compound C1=CC=C2C(OCC=C)=NS(=O)(=O)C2=C1 WHHIPMZEDGBUCC-UHFFFAOYSA-N 0.000 description 1
239000001294 propane Substances 0.000 description 1
239000003380 propellant Substances 0.000 description 1
FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 1
239000003531 protein hydrolysate Substances 0.000 description 1
239000008262 pumice Substances 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
239000010453 quartz Substances 0.000 description 1
239000011435 rock Substances 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
229910052624 sepiolite Inorganic materials 0.000 description 1
235000019355 sepiolite Nutrition 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
235000017557 sodium bicarbonate Nutrition 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
238000003756 stirring Methods 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
230000009885 systemic effect Effects 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D275/00—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings
- C07D275/04—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings condensed with carbocyclic rings or ring systems
- C07D275/06—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings condensed with carbocyclic rings or ring systems with hetero atoms directly attached to the ring sulfur atom
- 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
- A01N47/00—Biocides, 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
- A01N47/08—Biocides, 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 one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/38—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< where at least one nitrogen atom is part of a heterocyclic ring; Thio analogues thereof
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents

Landscapes

Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Dentistry (AREA)
Engineering & Computer Science (AREA)
Plant Pathology (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
General Chemical & Material Sciences (AREA)
Veterinary Medicine (AREA)
Chemical Kinetics & Catalysis (AREA)
Communicable Diseases (AREA)
Medicinal Chemistry (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Pharmacology & Pharmacy (AREA)
Animal Behavior & Ethology (AREA)
Public Health (AREA)
Oncology (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Saccharide Compounds (AREA)
Cosmetics (AREA)
Thiazole And Isothizaole Compounds (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Steroid Compounds (AREA)
Plural Heterocyclic Compounds (AREA)
Indole Compounds (AREA)

DD85280522A 1984-09-12 1985-09-11 Acylierte saccharin-derivate DD239516A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19843433391 DE3433391A1 (de)	1984-09-12	1984-09-12	Acylierte saccharin-derivate

Publications (1)

Publication Number	Publication Date
DD239516A5 true DD239516A5 (de)	1986-10-01

Family

ID=6245167

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD85280522A DD239516A5 (de)	1984-09-12	1985-09-11	Acylierte saccharin-derivate

Country Status (16)

Country	Link
US (1)	US4713389A (da)
EP (1)	EP0177740B1 (da)
JP (1)	JPS6168477A (da)
KR (1)	KR860002485A (da)
AT (1)	ATE37543T1 (da)
AU (1)	AU571734B2 (da)
BR (1)	BR8504387A (da)
DD (1)	DD239516A5 (da)
DE (2)	DE3433391A1 (da)
DK (1)	DK413385A (da)
ES (1)	ES8605496A1 (da)
GR (1)	GR852188B (da)
HU (1)	HUT39966A (da)
IL (1)	IL76331A0 (da)
PT (1)	PT81081B (da)
ZA (1)	ZA856951B (da)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH07171715A (ja) *	1992-02-10	1995-07-11	Takeda Seibiyoushiyo:Kk	ナットの不良品選別機
KR101055954B1 (ko)	2002-10-30	2011-08-09	바스프 에스이	이관능성 페닐이소(티오)시아네이트, 그의 제조 방법 및그의 제조를 위한 중간체 생성물
US7169933B2 (en) *	2003-11-14	2007-01-30	3M Innovative Properties Company	N-sulfonylaminocarbonyl containing compounds
US7423155B2 (en) *	2003-11-14	2008-09-09	3M Innovative Properties Company	N-sulfonyldicarboximide containing tethering compounds
US7943388B2 (en)	2003-11-14	2011-05-17	3M Innovative Properties Company	Acoustic sensors and methods
US7361767B2 (en) *	2003-11-14	2008-04-22	3M Innovative Properties Company	N-sulfonyldicarboximide containing tethering compounds
US7402678B2 (en)	2004-12-17	2008-07-22	3M Innovative Properties Company	Multifunctional amine capture agents
WO2005066121A2 (en) *	2003-12-30	2005-07-21	3M Innovative Properties Company	Multifunctional amine capture agents
US7342082B2 (en)	2004-12-17	2008-03-11	3M Innovative Properties Company	Soluble polymers as amine capture agents and methods
US7544755B2 (en)	2005-09-30	2009-06-09	3M Innovative Properties Company	Crosslinked polymers with amine binding groups
US7544754B2 (en)	2005-09-30	2009-06-09	3M Innovative Properties Company	Crosslinked polymers with amine binding groups
US7544756B2 (en)	2005-09-30	2009-06-09	3M Innovative Properties Company	Crosslinked polymers with amine binding groups

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3264314A (en) *	1965-06-28	1966-08-02	Monsanto Co	Halogenated phenylcarbamoyl saccharin
US3699228A (en) *	1968-10-25	1972-10-17	Nihon Nahyaku Co Ltd	Carbamoyl saccharin derivatives as fungicides
JPS4829134B1 (da) *	1970-10-08	1973-09-07
HU188291B (en) *	1981-06-11	1986-03-28	Chionin Gyogyszer Es Vegyeszetei Termekek Gyara Rt,Hu	Process for producing sulfimide derivatives of n-carbamoyl-benzoic acid

1984
- 1984-09-12 DE DE19843433391 patent/DE3433391A1/de not_active Withdrawn
1985
- 1985-08-31 AT AT85110995T patent/ATE37543T1/de not_active IP Right Cessation
- 1985-08-31 EP EP85110995A patent/EP0177740B1/de not_active Expired
- 1985-08-31 DE DE8585110995T patent/DE3565261D1/de not_active Expired
- 1985-09-03 PT PT81081A patent/PT81081B/pt unknown
- 1985-09-09 IL IL76331A patent/IL76331A0/xx unknown
- 1985-09-10 US US06/774,271 patent/US4713389A/en not_active Expired - Fee Related
- 1985-09-10 GR GR852188A patent/GR852188B/el unknown
- 1985-09-11 KR KR1019850006641A patent/KR860002485A/ko not_active Withdrawn
- 1985-09-11 DK DK413385A patent/DK413385A/da not_active Application Discontinuation
- 1985-09-11 JP JP60199614A patent/JPS6168477A/ja active Pending
- 1985-09-11 BR BR8504387A patent/BR8504387A/pt unknown
- 1985-09-11 ZA ZA856951A patent/ZA856951B/xx unknown
- 1985-09-11 DD DD85280522A patent/DD239516A5/de unknown
- 1985-09-11 AU AU47384/85A patent/AU571734B2/en not_active Ceased
- 1985-09-11 HU HU853430A patent/HUT39966A/hu unknown
- 1985-09-11 ES ES546877A patent/ES8605496A1/es not_active Expired

Also Published As

Publication number	Publication date
DK413385A (da)	1986-03-13
EP0177740A1 (de)	1986-04-16
HUT39966A (en)	1986-11-28
IL76331A0 (en)	1986-01-31
PT81081A (en)	1985-10-01
DE3565261D1 (en)	1988-11-03
ATE37543T1 (de)	1988-10-15
ES8605496A1 (es)	1986-03-16
AU4738485A (en)	1986-03-20
EP0177740B1 (de)	1988-09-28
JPS6168477A (ja)	1986-04-08
KR860002485A (ko)	1986-04-26
US4713389A (en)	1987-12-15
GR852188B (da)	1986-01-10
PT81081B (en)	1987-07-10
DE3433391A1 (de)	1986-03-20
DK413385D0 (da)	1985-09-11
BR8504387A (pt)	1986-07-08
ES546877A0 (es)	1986-03-16
AU571734B2 (en)	1988-04-21
ZA856951B (en)	1986-04-30

Publication	Publication Date	Title
EP0334135A2 (de)	1989-09-27	Trisubstituierte 1,3,5-Triazin-2,4,6-trione
EP0177740B1 (de)	1988-09-28	Acylierte Saccharin-Derivate
EP0248288A2 (de)	1987-12-09	Trisubstituierte 1,3,5-Triazin-2,4,6-trione
EP0334134A1 (de)	1989-09-27	3,7-Disubstituierte Benzthiazolone
EP0226051A1 (de)	1987-06-24	Fungizide Verwendung von Tetrahydrobenzothienylharnstoff-Derivaten
EP0205076B1 (de)	1988-05-04	Benzaldoxim-carbamat-Derivate
EP0438717A2 (de)	1991-07-31	Trisubstituierte 1,2,4-Triazin-3,5-dione und neue Zwischenprodukte
EP0158957B1 (de)	1989-01-18	Allophanat-Derivate
DE4000624A1 (de)	1991-07-18	Fungizide verwendung von trisubstituierten 1,3,5-triazin-2,4,6-trionen, neue trisubstituierte 1,3,5-triazin-2,4,6-trione und verfahren zu ihrer herstellung
EP0122553A1 (de)	1984-10-24	N-Sulfenylierte Phenethylsulfonamide
EP0283777A1 (de)	1988-09-28	Benzaldoxim-Derivate
EP0055429B1 (de)	1984-03-14	N-Sulfenylierte Allophanate, Verfahren zu ihrer Herstellung und ihre Verwendung als Fungizide
EP0422461A2 (de)	1991-04-17	Trisubstituierte 1,3,5-Triazin-2,4,6-trione
DD248953A5 (de)	1987-08-26	Schaedlingsbekaempfungsmittel
DD241544A5 (de)	1986-12-17	Schaedlingsbekaempfungsmittel
EP0269929A1 (de)	1988-06-08	Chlor-1,2,4-oxadiazole
EP0286970A2 (de)	1988-10-19	Alpha-Methylsulfonyl-benzaldoxim-Derivate
EP0391188A1 (de)	1990-10-10	Fungizide Mittel auf Basis von teilweise bekannten nitrosubstituierten Benzthiazolonen, neue nitrosubstituierte Benzthiazolone und Verfahren zu ihrer Herstellung
EP0281909A2 (de)	1988-09-14	Benzaldoxim-carbamat-Derivate
EP0213566A2 (de)	1987-03-11	N-Sulfenylierte Benzosulfonsäureamide
EP0286964A2 (de)	1988-10-19	Alpha-Methylsulfonyl-benzaldoximcarbamate
DE3520618A1 (de)	1986-12-11	Fungizide mittel auf benzaldoxim-derivat-basis
EP0236919A2 (de)	1987-09-16	Phenylsulfonyl-pyridinaldoxime
EP0236897A1 (de)	1987-09-16	Arylsulfonyl-pyridinaldoxim-Derivate
DD231480A5 (de)	1986-01-02	Pflanzenschutzmittel