DD248727A5 - Schaedlingsbekaempfungsmittel - Google Patents

Schaedlingsbekaempfungsmittel Download PDF

Info

Publication number: DD248727A5
Authority: DD; German Democratic Republic
Prior art keywords: och; formula; fluorine; chlorine; optionally substituted
Prior art date: 1985-08-06

Application number

DD86293406A

Other languages

German (de)

English (en)

Inventor

Christa Fest

Rolf Kirsten

Joachim Kluth

Klaus-Helmut Mueller

Theodor Pfister

Uwe Priesnitz

Hans-Jochen Riebel

Wolfgang Roy

Hans-Joachim Santel

Robert R Schmidt

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.)

1985-08-06

Filing date

1986-08-04

Publication date

1987-08-19

1986-08-04 Application filed by ��@��k�� filed Critical ��@��k��

1987-08-19 Publication of DD248727A5 publication Critical patent/DD248727A5/de

Links

238000000034 method Methods 0.000 claims abstract description 33
238000002360 preparation method Methods 0.000 claims abstract description 19
239000004009 herbicide Substances 0.000 claims abstract description 8
239000004606 Fillers/Extenders Substances 0.000 claims abstract description 4
239000004094 surface-active agent Substances 0.000 claims abstract description 4
239000000460 chlorine Chemical group 0.000 claims description 39
239000011737 fluorine Chemical group 0.000 claims description 34
229910052731 fluorine Inorganic materials 0.000 claims description 34
-1 hydroxy, cyclopropyl Chemical group 0.000 claims description 31
229910052801 chlorine Inorganic materials 0.000 claims description 30
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 29
125000001153 fluoro group Chemical group F* 0.000 claims description 24
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 10
125000001309 chloro group Chemical group Cl* 0.000 claims description 9
239000001257 hydrogen Substances 0.000 claims description 8
229910052739 hydrogen Inorganic materials 0.000 claims description 8
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 8
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 6
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 5
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 5
229910052794 bromium Inorganic materials 0.000 claims description 5
239000004202 carbamide Substances 0.000 claims description 4
125000000217 alkyl group Chemical class 0.000 claims description 3
125000004414 alkyl thio group Chemical group 0.000 claims description 3
125000003118 aryl group Chemical class 0.000 claims description 3
125000003342 alkenyl group Chemical class 0.000 claims description 2
125000000304 alkynyl group Chemical class 0.000 claims description 2
125000003710 aryl alkyl group Chemical class 0.000 claims description 2
125000001316 cycloalkyl alkyl group Chemical class 0.000 claims description 2
125000000753 cycloalkyl group Chemical class 0.000 claims description 2
230000008635 plant growth Effects 0.000 claims 2
239000000203 mixture Substances 0.000 abstract description 21
230000002363 herbicidal effect Effects 0.000 abstract description 7
239000000575 pesticide Substances 0.000 abstract description 5
239000003795 chemical substances by application Substances 0.000 abstract description 4
150000001875 compounds Chemical class 0.000 description 42
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 22
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 21
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239000007858 starting material Substances 0.000 description 16
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238000006243 chemical reaction Methods 0.000 description 11
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239000002904 solvent Substances 0.000 description 10
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239000003085 diluting agent Substances 0.000 description 8
239000000243 solution Substances 0.000 description 8
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239000002585 base Substances 0.000 description 7
239000012973 diazabicyclooctane Substances 0.000 description 7
230000000694 effects Effects 0.000 description 7
239000003995 emulsifying agent Substances 0.000 description 7
238000009472 formulation Methods 0.000 description 7
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
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239000000370 acceptor Substances 0.000 description 6
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239000004480 active ingredient Substances 0.000 description 6
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239000002689 soil Substances 0.000 description 5
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229910052783 alkali metal Inorganic materials 0.000 description 4
125000004093 cyano group Chemical group *C#N 0.000 description 4
239000003960 organic solvent Substances 0.000 description 4
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XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical class [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
150000001340 alkali metals Chemical class 0.000 description 3
229910052784 alkaline earth metal Inorganic materials 0.000 description 3
125000002877 alkyl aryl group Chemical group 0.000 description 3
239000000969 carrier Substances 0.000 description 3
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238000001035 drying Methods 0.000 description 3
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150000002170 ethers Chemical class 0.000 description 3
239000005457 ice water Substances 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
239000011707 mineral Substances 0.000 description 3
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239000010695 polyglycol Substances 0.000 description 3
239000011541 reaction mixture Substances 0.000 description 3
VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
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125000001424 substituent group Chemical group 0.000 description 3
238000010626 work up procedure Methods 0.000 description 3
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JRZJOMJEPLMPRA-UHFFFAOYSA-N 1-nonene Chemical compound CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
WADSJYLPJPTMLN-UHFFFAOYSA-N 3-(cycloundecen-1-yl)-1,2-diazacycloundec-2-ene Chemical compound C1CCCCCCCCC=C1C1=NNCCCCCCCC1 WADSJYLPJPTMLN-UHFFFAOYSA-N 0.000 description 2
VHYFNPMBLIVWCW-UHFFFAOYSA-N 4-Dimethylaminopyridine Chemical compound CN(C)C1=CC=NC=C1 VHYFNPMBLIVWCW-UHFFFAOYSA-N 0.000 description 2
RTNUTCOTGVKVBR-UHFFFAOYSA-N 4-chlorotriazine Chemical class ClC1=CC=NN=N1 RTNUTCOTGVKVBR-UHFFFAOYSA-N 0.000 description 2
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235000012211 aluminium silicate Nutrition 0.000 description 1
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XXMNTYMQGKSNPR-UHFFFAOYSA-N benzene-1,2-disulfonic acid;hydrochloride Chemical compound Cl.OS(=O)(=O)C1=CC=CC=C1S(O)(=O)=O XXMNTYMQGKSNPR-UHFFFAOYSA-N 0.000 description 1
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239000011230 binding agent Substances 0.000 description 1
238000009835 boiling Methods 0.000 description 1
229910052796 boron Inorganic materials 0.000 description 1
AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
239000000920 calcium hydroxide Substances 0.000 description 1
229910001861 calcium hydroxide Inorganic materials 0.000 description 1
239000001768 carboxy methyl cellulose Substances 0.000 description 1
235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
239000008112 carboxymethyl-cellulose Substances 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
150000008422 chlorobenzenes Chemical class 0.000 description 1
235000020971 citrus fruits Nutrition 0.000 description 1
239000010941 cobalt Substances 0.000 description 1
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GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
235000016213 coffee Nutrition 0.000 description 1
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150000002430 hydrocarbons Chemical class 0.000 description 1
150000003840 hydrochlorides Chemical class 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
239000003701 inert diluent Substances 0.000 description 1
239000001023 inorganic pigment Substances 0.000 description 1
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PUIYMUZLKQOUOZ-UHFFFAOYSA-N isoproturon Chemical compound CC(C)C1=CC=C(NC(=O)N(C)C)C=C1 PUIYMUZLKQOUOZ-UHFFFAOYSA-N 0.000 description 1
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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
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VHCNQEUWZYOAEV-UHFFFAOYSA-N metamitron Chemical compound O=C1N(N)C(C)=NN=C1C1=CC=CC=C1 VHCNQEUWZYOAEV-UHFFFAOYSA-N 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
SPUACDWLOLSOQO-UHFFFAOYSA-M methoxyazanium;chloride Chemical compound [Cl-].CO[NH3+] SPUACDWLOLSOQO-UHFFFAOYSA-M 0.000 description 1
125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
FOXFZRUHNHCZPX-UHFFFAOYSA-N metribuzin Chemical compound CSC1=NN=C(C(C)(C)C)C(=O)N1N FOXFZRUHNHCZPX-UHFFFAOYSA-N 0.000 description 1
238000002156 mixing Methods 0.000 description 1
229910052750 molybdenum Inorganic materials 0.000 description 1
239000011733 molybdenum Substances 0.000 description 1
229940042880 natural phospholipid Drugs 0.000 description 1
239000005645 nematicide Substances 0.000 description 1
125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
235000014571 nuts Nutrition 0.000 description 1
239000003921 oil Substances 0.000 description 1
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239000011368 organic material Substances 0.000 description 1
239000012074 organic phase Substances 0.000 description 1
150000002902 organometallic compounds Chemical class 0.000 description 1
229910052625 palygorskite Inorganic materials 0.000 description 1
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239000003208 petroleum Substances 0.000 description 1
125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
150000003904 phospholipids Chemical class 0.000 description 1
239000001007 phthalocyanine dye 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
229910000027 potassium carbonate Inorganic materials 0.000 description 1
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000003531 protein hydrolysate Substances 0.000 description 1
108090000623 proteins and genes Proteins 0.000 description 1
239000008262 pumice Substances 0.000 description 1
239000010453 quartz Substances 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
238000010992 reflux Methods 0.000 description 1
239000005871 repellent Substances 0.000 description 1
230000002940 repellent Effects 0.000 description 1
239000011435 rock Substances 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
SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
239000007921 spray Substances 0.000 description 1
238000003892 spreading Methods 0.000 description 1
125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
230000002195 synergetic effect Effects 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
235000013616 tea Nutrition 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 description 1
229960000278 theophylline Drugs 0.000 description 1
OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
QRVVIQWKEKNPHH-UHFFFAOYSA-N triazin-4-ylcyanamide Chemical class N#CNC1=CC=NN=N1 QRVVIQWKEKNPHH-UHFFFAOYSA-N 0.000 description 1
125000005034 trifluormethylthio group Chemical group FC(S*)(F)F 0.000 description 1
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
238000001665 trituration Methods 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
235000014101 wine Nutrition 0.000 description 1
239000011701 zinc Substances 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D521/00—Heterocyclic compounds containing unspecified hetero rings
- 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
- A01N51/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds having the sequences of atoms O—N—S, X—O—S, N—N—S, O—N—N or O-halogen, regardless of the number of bonds each atom has and with no atom of these sequences forming part of a heterocyclic ring

Landscapes

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)
Agricultural Chemicals And Associated Chemicals (AREA)
Plural Heterocyclic Compounds (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

DD86293406A 1985-08-06 1986-08-04 Schaedlingsbekaempfungsmittel DD248727A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19853528100 DE3528100A1 (de)	1985-08-06	1985-08-06	1-(2-oxyaminosulfonylphenylsulfonyl) -3-triazinyl-harnstoffe

Publications (1)

Publication Number	Publication Date
DD248727A5 true DD248727A5 (de)	1987-08-19

Family

ID=6277766

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD86293406A DD248727A5 (de)	1985-08-06	1986-08-04	Schaedlingsbekaempfungsmittel

Country Status (13)

Country	Link
EP (1)	EP0213378A1 (da)
JP (1)	JPS6233163A (da)
KR (1)	KR870002103A (da)
AU (1)	AU6093586A (da)
BR (1)	BR8603715A (da)
CA (1)	CA1242720A (da)
DD (1)	DD248727A5 (da)
DE (1)	DE3528100A1 (da)
DK (1)	DK372486A (da)
ES (1)	ES2000130A6 (da)
HU (1)	HUT44136A (da)
IL (1)	IL79604A0 (da)
ZA (1)	ZA865860B (da)

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DK536582A (da) *	1981-12-07	1983-06-08	Du Pont	Herbicide sulfonamider
EP0124295B1 (en) *	1983-04-04	1991-04-03	E.I. Du Pont De Nemours And Company	Stabilized aqueous formulations of sulfonylureas
US4548638A (en) *	1983-08-22	1985-10-22	E. I. Du Pont De Nemours And Company	Herbicidal sulfonylureas

1985
- 1985-08-06 DE DE19853528100 patent/DE3528100A1/de not_active Withdrawn
1986
- 1986-07-25 EP EP86110264A patent/EP0213378A1/de not_active Withdrawn
- 1986-08-01 CA CA000515170A patent/CA1242720A/en not_active Expired
- 1986-08-04 DD DD86293406A patent/DD248727A5/de unknown
- 1986-08-04 IL IL79604A patent/IL79604A0/xx unknown
- 1986-08-05 JP JP61182879A patent/JPS6233163A/ja active Pending
- 1986-08-05 BR BR8603715A patent/BR8603715A/pt unknown
- 1986-08-05 ZA ZA865860A patent/ZA865860B/xx unknown
- 1986-08-05 DK DK372486A patent/DK372486A/da not_active Application Discontinuation
- 1986-08-05 KR KR1019860006458A patent/KR870002103A/ko not_active Withdrawn
- 1986-08-06 AU AU60935/86A patent/AU6093586A/en not_active Abandoned
- 1986-08-06 ES ES8600905A patent/ES2000130A6/es not_active Expired
- 1986-08-06 HU HU863428A patent/HUT44136A/hu unknown

Also Published As

Publication number	Publication date
CA1242720A (en)	1988-10-04
KR870002103A (ko)	1987-03-30
ES2000130A6 (es)	1987-12-16
BR8603715A (pt)	1987-03-10
DE3528100A1 (de)	1987-02-19
HUT44136A (en)	1988-02-29
AU6093586A (en)	1987-02-12
DK372486A (da)	1987-02-07
ZA865860B (en)	1987-04-29
DK372486D0 (da)	1986-08-05
JPS6233163A (ja)	1987-02-13
EP0213378A1 (de)	1987-03-11
IL79604A0 (en)	1986-11-30

Publication	Publication Date	Title
EP0121082A1 (de)	1984-10-10	Guanidin-Derivate
DE3801113A1 (de)	1989-02-02	Substituierte triazine
EP0173958A2 (de)	1986-03-12	1-(2-Oxyaminocarbonylphenylsulfonyl)-3-heteroaryl-harnstoffe
DD238522A5 (de)	1986-08-27	Herbizide mittel
EP0173314B1 (de)	1989-04-12	Benzodisultame
EP0173322B1 (de)	1988-12-28	(1-(2-Oxyaminosulfonylphenylsulfonyl)-3-heteroaryl-harnstoffe
EP0224078A1 (de)	1987-06-03	Thienylsulfonylguanidin-Derivate
DD237784A5 (de)	1986-07-30	Herbizide mittel
DE3431916A1 (de)	1986-03-13	Fluoralkoxyphenylsulfonylguanidine
EP0173320A1 (de)	1986-03-05	Substituierte Carbonylphenylsulfonylguanidine
EP0217038B1 (de)	1989-06-07	Benzo-[b]-1,4,5,7-dithiadiazepin-1,1,4,4-tetraoxydderivate
DE3517842A1 (de)	1986-03-13	Sulfonylguanidinopyrimidin-derivate
DD248727A5 (de)	1987-08-19	Schaedlingsbekaempfungsmittel
DD237782A5 (de)	1986-07-30	Herbizide mittel
DE3517821A1 (de)	1986-03-13	Sulfonylguanidinotriazin-derivate
EP0173316A2 (de)	1986-03-05	1-(2-Oxyaminosulfonylphenylsulfonyl)-3-heteroaryl-iso-(thio)-harnstoffe
DD257380A5 (de)	1988-06-15	Herbizide mittel
DE3431913A1 (de)	1986-03-13	Oxyguanidin-derivate
DE3431933A1 (de)	1986-03-06	Heteroarylthioharnstoffe
DE3412946A1 (de)	1985-10-17	3-(2,2-tetramethylen-propyl)-1,3,5-triazin-2,4-dione
DD237780A5 (de)	1986-07-30	Herbizide mittel
EP0264021A2 (de)	1988-04-20	0-Aryl-N'-(triazin-2-yl)-isoharnstoffe
DE3601801A1 (de)	1987-07-23	Herbizide mittel
DE3605549A1 (de)	1987-08-27	Sulfonylamidino-oxazacycloalkane
DD238524A5 (de)	1986-08-27	Herbizide mittel