PH26866A - Heterocyclic N-acylsulfonamides and their use as herbicides and plant growth regulators - Google Patents

Heterocyclic N-acylsulfonamides and their use as herbicides and plant growth regulators Download PDF

Info

Publication number: PH26866A
Authority: PH; Philippines
Prior art keywords: melting point; continuation; formula; continuation example; och
Prior art date: 1988-08-02

Application number

PH39022A

Other languages

English (en)

Inventor

Oswald Ort

Lothar Willms

Klaus Bauer

Hermann Bieringer

Arno Schulz

Original Assignee

Hoechst Ag

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.)

1988-08-02

Filing date

1989-07-31

Publication date

1992-11-16

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=6360084&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PH26866(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

1989-07-31 Application filed by Hoechst Ag filed Critical Hoechst Ag

1992-11-16 Publication of PH26866A publication Critical patent/PH26866A/en

Links

125000000623 heterocyclic group Chemical group 0.000 title claims description 14
239000004009 herbicide Substances 0.000 title description 5
239000005648 plant growth regulator Substances 0.000 title 1
150000001875 compounds Chemical class 0.000 claims description 64
229910052739 hydrogen Inorganic materials 0.000 claims description 33
239000001257 hydrogen Substances 0.000 claims description 32
238000000034 method Methods 0.000 claims description 22
229910052736 halogen Inorganic materials 0.000 claims description 20
150000002367 halogens Chemical class 0.000 claims description 20
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 20
230000002363 herbicidal effect Effects 0.000 claims description 15
150000003839 salts Chemical class 0.000 claims description 14
125000000217 alkyl group Chemical group 0.000 claims description 12
229910052801 chlorine Inorganic materials 0.000 claims description 12
229910052731 fluorine Inorganic materials 0.000 claims description 11
150000002431 hydrogen Chemical class 0.000 claims description 10
239000003795 chemical substances by application Substances 0.000 claims description 9
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 8
229910052799 carbon Inorganic materials 0.000 claims description 7
125000001188 haloalkyl group Chemical group 0.000 claims description 7
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
229910052740 iodine Inorganic materials 0.000 claims description 5
239000000654 additive Substances 0.000 claims description 4
230000001105 regulatory effect Effects 0.000 claims description 4
230000001276 controlling effect Effects 0.000 claims description 3
230000008635 plant growth Effects 0.000 claims description 3
125000004430 oxygen atom Chemical group O* 0.000 claims 1
229910052717 sulfur Inorganic materials 0.000 claims 1
125000004434 sulfur atom Chemical group 0.000 claims 1
238000002844 melting Methods 0.000 description 160
230000008018 melting Effects 0.000 description 160
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 68
239000000203 mixture Substances 0.000 description 43
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 32
-1 monocyclic pyridinecarboxamides Chemical class 0.000 description 28
239000000460 chlorine Substances 0.000 description 26
241000196324 Embryophyta Species 0.000 description 23
239000000243 solution Substances 0.000 description 19
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 19
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 18
238000006243 chemical reaction Methods 0.000 description 17
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 16
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 16
238000003756 stirring Methods 0.000 description 15
238000002360 preparation method Methods 0.000 description 13
239000013543 active substance Substances 0.000 description 12
239000002253 acid Substances 0.000 description 11
239000011734 sodium Substances 0.000 description 11
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 10
239000002585 base Substances 0.000 description 10
229910052794 bromium Inorganic materials 0.000 description 10
244000309464 bull Species 0.000 description 10
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
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 9
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 9
238000009472 formulation Methods 0.000 description 9
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 9
229910052708 sodium Inorganic materials 0.000 description 9
239000000126 substance Substances 0.000 description 9
239000007787 solid Substances 0.000 description 8
239000002904 solvent Substances 0.000 description 8
239000011575 calcium Substances 0.000 description 7
239000012141 concentrate Substances 0.000 description 7
239000000843 powder Substances 0.000 description 7
150000003254 radicals Chemical class 0.000 description 7
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
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JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 6
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
241001233957 eudicotyledons Species 0.000 description 6
239000008187 granular material Substances 0.000 description 6
230000012010 growth Effects 0.000 description 6
239000000543 intermediate Substances 0.000 description 6
239000012074 organic phase Substances 0.000 description 6
239000012071 phase Substances 0.000 description 6
229920000728 polyester Polymers 0.000 description 6
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 6
239000002689 soil Substances 0.000 description 6
FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 6
241000209510 Liliopsida Species 0.000 description 5
150000001412 amines Chemical class 0.000 description 5
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 5
238000000227 grinding Methods 0.000 description 5
229910000029 sodium carbonate Inorganic materials 0.000 description 5
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 4
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 4
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 4
XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 4
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 4
RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 4
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
238000009835 boiling Methods 0.000 description 4
244000038559 crop plants Species 0.000 description 4
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
238000005516 engineering process Methods 0.000 description 4
239000000706 filtrate Substances 0.000 description 4
239000011777 magnesium Substances 0.000 description 4
229910052749 magnesium Inorganic materials 0.000 description 4
229910052751 metal Inorganic materials 0.000 description 4
239000002184 metal Substances 0.000 description 4
238000002156 mixing Methods 0.000 description 4
CTSLXHKWHWQRSH-UHFFFAOYSA-N oxalyl chloride Chemical compound ClC(=O)C(Cl)=O CTSLXHKWHWQRSH-UHFFFAOYSA-N 0.000 description 4
239000000047 product Substances 0.000 description 4
OISVCGZHLKNMSJ-UHFFFAOYSA-N 2,6-dimethylpyridine Chemical compound CC1=CC=CC(C)=N1 OISVCGZHLKNMSJ-UHFFFAOYSA-N 0.000 description 3
VHYFNPMBLIVWCW-UHFFFAOYSA-N 4-dimethylaminopyridine Substances CN(C)C1=CC=NC=C1 VHYFNPMBLIVWCW-UHFFFAOYSA-N 0.000 description 3
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 3
QOSSAOTZNIDXMA-UHFFFAOYSA-N Dicylcohexylcarbodiimide Chemical compound C1CCCCC1N=C=NC1CCCCC1 QOSSAOTZNIDXMA-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
125000000304 alkynyl group Chemical group 0.000 description 3
230000015572 biosynthetic process Effects 0.000 description 3
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 3
229950005499 carbon tetrachloride Drugs 0.000 description 3
150000001735 carboxylic acids Chemical class 0.000 description 3
150000001805 chlorine compounds Chemical class 0.000 description 3
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 3
235000014113 dietary fatty acids Nutrition 0.000 description 3
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 3
239000000839 emulsion Substances 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
239000000194 fatty acid Substances 0.000 description 3
229930195729 fatty acid Natural products 0.000 description 3
IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 3
229910000041 hydrogen chloride Inorganic materials 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 3
239000007788 liquid Substances 0.000 description 3
125000000896 monocarboxylic acid group Chemical group 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
150000002825 nitriles Chemical class 0.000 description 3
229910052757 nitrogen Inorganic materials 0.000 description 3
229910000027 potassium carbonate Inorganic materials 0.000 description 3
239000002243 precursor Substances 0.000 description 3
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 3
FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 3
241000894007 species Species 0.000 description 3
229940124530 sulfonamide Drugs 0.000 description 3
150000003456 sulfonamides Chemical class 0.000 description 3
239000000725 suspension Substances 0.000 description 3
238000003786 synthesis reaction Methods 0.000 description 3
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 2
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 2
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 description 2
125000001541 3-thienyl group Chemical group S1C([H])=C([*])C([H])=C1[H] 0.000 description 2
FPSPPRZKBUVEJQ-UHFFFAOYSA-N 4,6-dimethoxypyrimidine Chemical compound COC1=CC(OC)=NC=N1 FPSPPRZKBUVEJQ-UHFFFAOYSA-N 0.000 description 2
101710179738 6,7-dimethyl-8-ribityllumazine synthase 1 Proteins 0.000 description 2
HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
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AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 2
101710186608 Lipoyl synthase 1 Proteins 0.000 description 2
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101710090391 Lipoyl synthase 1, mitochondrial Proteins 0.000 description 2
WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
240000007594 Oryza sativa Species 0.000 description 2
235000007164 Oryza sativa Nutrition 0.000 description 2
KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
239000004372 Polyvinyl alcohol Substances 0.000 description 2
XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
240000006694 Stellaria media Species 0.000 description 2
240000008042 Zea mays Species 0.000 description 2
235000002017 Zea mays subsp mays Nutrition 0.000 description 2
241001148683 Zostera marina Species 0.000 description 2
KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 2
229910021529 ammonia Inorganic materials 0.000 description 2
150000001448 anilines Chemical class 0.000 description 2
239000000010 aprotic solvent Substances 0.000 description 2
239000008346 aqueous phase Substances 0.000 description 2
239000007864 aqueous solution Substances 0.000 description 2
239000004202 carbamide Substances 0.000 description 2
239000001569 carbon dioxide Substances 0.000 description 2
229910002092 carbon dioxide Inorganic materials 0.000 description 2
PFKFTWBEEFSNDU-UHFFFAOYSA-N carbonyldiimidazole Chemical compound C1=CN=CN1C(=O)N1C=CN=C1 PFKFTWBEEFSNDU-UHFFFAOYSA-N 0.000 description 2
239000000969 carrier Substances 0.000 description 2
239000003054 catalyst Substances 0.000 description 2
238000004587 chromatography analysis Methods 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
238000001035 drying Methods 0.000 description 2
239000003480 eluent Substances 0.000 description 2
150000002170 ethers Chemical class 0.000 description 2
150000002191 fatty alcohols Chemical class 0.000 description 2
239000003337 fertilizer Substances 0.000 description 2
238000001914 filtration Methods 0.000 description 2
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239000003630 growth substance Substances 0.000 description 2
230000007062 hydrolysis Effects 0.000 description 2
238000006460 hydrolysis reaction Methods 0.000 description 2
DOUHZFSGSXMPIE-UHFFFAOYSA-N hydroxidooxidosulfur(.) Chemical compound [O]SO DOUHZFSGSXMPIE-UHFFFAOYSA-N 0.000 description 2
229910052744 lithium Inorganic materials 0.000 description 2
239000000463 material Substances 0.000 description 2
229910000000 metal hydroxide Inorganic materials 0.000 description 2
150000004692 metal hydroxides Chemical class 0.000 description 2
GRMQHXKUKDWTPH-UHFFFAOYSA-N methyl 2-(4,6-dichloropyrimidin-2-yl)acetate Chemical compound COC(=O)CC1=NC(Cl)=CC(Cl)=N1 GRMQHXKUKDWTPH-UHFFFAOYSA-N 0.000 description 2
VAMXMNNIEUEQDV-UHFFFAOYSA-N methyl anthranilate Chemical compound COC(=O)C1=CC=CC=C1N VAMXMNNIEUEQDV-UHFFFAOYSA-N 0.000 description 2
125000001477 organic nitrogen group Chemical group 0.000 description 2
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235000009566 rice Nutrition 0.000 description 2
239000004576 sand Substances 0.000 description 2
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239000000454 talc Substances 0.000 description 2
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PRXXMEMJCXTHTP-UHFFFAOYSA-N 4,6-dimethoxypyrimidine-2-carboxylic acid Chemical compound COC1=CC(OC)=NC(C(O)=O)=N1 PRXXMEMJCXTHTP-UHFFFAOYSA-N 0.000 description 1
LKSBWGAXXXJKPX-UHFFFAOYSA-N 4-methoxy-6-methylpyrimidine-2-carboxylic acid Chemical compound COC1=CC(C)=NC(C(O)=O)=N1 LKSBWGAXXXJKPX-UHFFFAOYSA-N 0.000 description 1
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Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
- 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/34—One oxygen atom
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/52—Two oxygen atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles 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
- C07D249/12—Oxygen or sulfur atoms
- 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
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- C07D251/14—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 with hydrogen or carbon atoms directly attached to at least one ring carbon atom
- C07D251/16—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 with hydrogen or carbon atoms directly attached to at least one ring carbon atom to only one ring carbon atom
- 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
- C07D251/14—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 with hydrogen or carbon atoms directly attached to at least one ring carbon atom
- C07D251/22—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 with hydrogen or carbon atoms directly attached to at least one ring carbon atom to two ring carbon atoms
- 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
- C07D251/14—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 with hydrogen or carbon atoms directly attached to at least one ring carbon atom
- C07D251/24—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 with hydrogen or carbon atoms directly attached to at least one ring carbon atom to three ring carbon atoms
- 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
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- C07D251/26—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 with only hetero atoms directly attached to ring carbon atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems

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)
Plural Heterocyclic Compounds (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)
Enzymes And Modification Thereof (AREA)
Pyridine Compounds (AREA)

PH39022A 1988-08-02 1989-07-31 Heterocyclic N-acylsulfonamides and their use as herbicides and plant growth regulators PH26866A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE3826230A DE3826230A1 (de)	1988-08-02	1988-08-02	Heterocyclische n-acylsufonamide, verfahren zu ihrer herstellung, sie enthaltende mittel und ihre verwendung als herbizide oder wachstumsregulatoren

Publications (1)

Publication Number	Publication Date
PH26866A true PH26866A (en)	1992-11-16

Family

ID=6360084

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
PH39022A PH26866A (en)	1988-08-02	1989-07-31	Heterocyclic N-acylsulfonamides and their use as herbicides and plant growth regulators

Country Status (15)

Country	Link
US (1)	US5053072A (es)
EP (1)	EP0353640B2 (es)
JP (1)	JP3117137B2 (es)
KR (1)	KR900003158A (es)
AU (1)	AU636299B2 (es)
BR (1)	BR8903885A (es)
DD (1)	DD283915A5 (es)
DE (2)	DE3826230A1 (es)
DK (1)	DK377389A (es)
ES (1)	ES2070870T5 (es)
HU (1)	HUT55001A (es)
IL (1)	IL91164A (es)
NZ (1)	NZ230136A (es)
PH (1)	PH26866A (es)
ZA (1)	ZA895852B (es)

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DE4029055A1 (de) *	1990-03-01	1991-09-05	Bayer Ag	Sulfonylierte pyrimidincarbonsaeureamide
GB9015916D0 (en) *	1990-07-19	1990-09-05	Schering Agrochemicals Ltd	Herbicides
DE4029753A1 (de) *	1990-09-20	1992-03-26	Basf Ag	Sulfonamide
US5411934A (en) *	1990-11-30	1995-05-02	Kumiai Chemical Industry Co., Ltd.	Alkanoic acid amide derivative or its salt, process for producing the same and herbicidal composition
GB9105297D0 (en) *	1991-03-13	1991-04-24	Schering Agrochemicals Ltd	Herbicides
US5502028A (en) *	1991-03-13	1996-03-26	Schering Agrochemicals Limited	Herbicidal pyrimidinyl or triazinyl haloacetic acid derivatives
RU2117662C1 (ru) *	1992-03-03	1998-08-20	Кумиай Кемикал Индастри Ко., Лтд.	Производные амида n-сульфонилкарбоновой кислоты, включающие n-содержащее 6-членное ароматическое кольцо, фунгицидная и гербицидная композиции и способы борьбы с сорняками и фитопатогенными грибками
DE4233338A1 (de) *	1992-10-05	1994-04-07	Bayer Ag	Sulfonylierte Triazincarbonsäureamide
US5491172A (en) *	1993-05-14	1996-02-13	Warner-Lambert Company	N-acyl sulfamic acid esters (or thioesters), N-acyl sulfonamides, and N-sulfonyl carbamic acid esters (or thioesters) as hypercholesterolemic agents
DE19616445A1 (de) *	1996-04-25	1997-11-06	Hoechst Schering Agrevo Gmbh	Substituierte Aminomethylphenylsulfonylharnstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung als Herbizide und Pflanzenwachstumsregulatoren
CA2208900C (en) *	1996-07-18	2006-08-01	Lonza Ag	Process for preparing 2-pyrimidinecarboxylates
CA2209258C (en) *	1996-07-18	2007-09-11	Lonza Ag	Method for preparing pyrimidin-2-ylacetic acid esters
US6093744A (en) *	1997-04-21	2000-07-25	Warner-Lambert Company	N-acyl sulfamic acid esters useful as hypocholesterolemic agents
AR037097A1 (es) *	2001-10-05	2004-10-20	Novartis Ag	Compuestos acilsulfonamidas, composiciones farmaceuticas y el uso de dichos compuestos para la preparacion de un medicamento
TW200510305A (en) *	2003-07-25	2005-03-16	Wyeth Corp	Process for the preparation of CPLA2 inhibitors
WO2005049593A2 (en)	2003-11-13	2005-06-02	Abbott Laboratories	N-acylsulfonamide apoptosis promoters
US7973161B2 (en)	2003-11-13	2011-07-05	Abbott Laboratories	Apoptosis promoters
US7767684B2 (en)	2003-11-13	2010-08-03	Abbott Laboratories	Apoptosis promoters
US8614318B2 (en)	2003-11-13	2013-12-24	Abbvie Inc.	Apoptosis promoters
PL1888550T3 (pl)	2005-05-12	2014-12-31	Abbvie Bahamas Ltd	Promotory apoptozy
US8624027B2 (en)	2005-05-12	2014-01-07	Abbvie Inc.	Combination therapy for treating cancer and diagnostic assays for use therein
JP5277168B2 (ja)	2006-09-05	2013-08-28	アボット・ラボラトリーズ	血小板過剰を治療するｂｃｌインヒビター
JP4839258B2 (ja)	2007-04-17	2011-12-21	山下ゴム株式会社	筒型防振装置
EP2463277B1 (en)	2009-08-07	2017-11-08	Kumiai Chemical Industry Co., Ltd.	Method for producing 4,6-dialkoxy-2-cyanomethylpyrimidine and synthetic intermediate thereof
PE20141468A1 (es)	2010-12-21	2014-11-05	Bayer Cropscience Lp	Mutantes tipo papel de lija de bacillus y metodos de uso de los mismo para mejorar el crecimiento vegetal, promover la salud de plantas y controlar enfermedades y plagas
MX2014002890A (es)	2011-09-12	2015-01-19	Bayer Cropscience Lp	Metodo para mejorar la salud y/o promover el crecimiento de una planta y/o mejorar la maduracion de frutos.
ES2940611T3 (es) *	2016-04-18	2023-05-09	Novartis Ag	Compuestos y composiciones para el tratamiento de afecciones asociadas a la actividad de NLRP
EP3914583A1 (en) *	2019-01-22	2021-12-01	Novartis AG	Compounds and compositions for treating conditions associated with nlrp activity

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AU526899B2 (en) *	1979-10-22	1983-02-03	E.I. Du Pont De Nemours And Company	Herbicidal pyridine sulfonamides
US4838925A (en) *	1986-04-25	1989-06-13	E. I. Du Pont De Nemours And Company	Heterocyclic acyl sulfonamides
DK366887A (da) †	1986-07-31	1988-05-13	Hoffmann La Roche	Pyrimidinderivater
DE3816703A1 (de) *	1988-05-17	1989-11-30	Hoechst Ag	Heterocyclisch substituierte phenoxysulfonylharnstoffe, verfahren zu ihrer herstellung und ihre verwendung als herbizide oder pflanzenwachstumsregulatoren
DE3909053A1 (de) *	1989-03-18	1990-09-20	Hoechst Ag	Phenoxysulfonylharnstoffe auf basis von 3-substituierten salicylsaeurealkylestern, verfahren zu ihrer herstellung und ihre verwendung als herbizide und pflanzenwachstumsregulatoren

1988
- 1988-08-02 DE DE3826230A patent/DE3826230A1/de not_active Withdrawn
1989
- 1989-07-28 ES ES89113916T patent/ES2070870T5/es not_active Expired - Lifetime
- 1989-07-28 DE DE58909172T patent/DE58909172D1/de not_active Expired - Fee Related
- 1989-07-28 EP EP89113916A patent/EP0353640B2/de not_active Expired - Lifetime
- 1989-07-31 IL IL9116489A patent/IL91164A/en not_active IP Right Cessation
- 1989-07-31 DD DD89331307A patent/DD283915A5/de not_active IP Right Cessation
- 1989-07-31 PH PH39022A patent/PH26866A/en unknown
- 1989-07-31 US US07/387,531 patent/US5053072A/en not_active Expired - Lifetime
- 1989-07-31 NZ NZ230136A patent/NZ230136A/en unknown
- 1989-08-01 KR KR1019890010964A patent/KR900003158A/ko not_active Withdrawn
- 1989-08-01 ZA ZA895852A patent/ZA895852B/xx unknown
- 1989-08-01 DK DK377389A patent/DK377389A/da not_active Application Discontinuation
- 1989-08-01 HU HU893924A patent/HUT55001A/hu unknown
- 1989-08-01 JP JP01198114A patent/JP3117137B2/ja not_active Expired - Fee Related
- 1989-08-01 AU AU39144/89A patent/AU636299B2/en not_active Ceased
- 1989-08-02 BR BR898903885A patent/BR8903885A/pt unknown

Also Published As

Publication number	Publication date
EP0353640B1 (de)	1995-04-12
JP3117137B2 (ja)	2000-12-11
EP0353640A3 (de)	1991-05-08
BR8903885A (pt)	1990-03-20
AU3914489A (en)	1990-02-08
IL91164A (en)	1994-11-28
ZA895852B (en)	1990-04-25
DD283915A5 (de)	1990-10-31
HUT55001A (en)	1991-04-29
EP0353640B2 (de)	2003-10-15
NZ230136A (en)	1991-12-23
DE58909172D1 (de)	1995-05-18
IL91164A0 (en)	1990-03-19
KR900003158A (ko)	1990-03-23
EP0353640A2 (de)	1990-02-07
DK377389A (da)	1990-02-03
ES2070870T5 (es)	2004-06-16
AU636299B2 (en)	1993-04-29
US5053072A (en)	1991-10-01
DK377389D0 (da)	1989-08-01
JPH02282371A (ja)	1990-11-19
ES2070870T3 (es)	1995-06-16
DE3826230A1 (de)	1990-02-08

Publication	Publication Date	Title
PH26866A (en)	1992-11-16	Heterocyclic N-acylsulfonamides and their use as herbicides and plant growth regulators
DE69222322T2 (de)	1998-02-26	Sulfonamide als herbizide
EP0083613B1 (en)	1988-06-01	N-phenylpyrazole derivatives useful as herbicides
DE4309969A1 (de)	1994-09-29	Substituierte heteroanellierte Imidazole
KR20150103174A (ko)	2015-09-09	살진균제로서의 3-알킬-5-플루오로-4-치환된-이미노-3,4-디히드로피리미딘-2(1h)-온 유도체
EP0338465B1 (de)	1993-06-02	1-Chlorpyrimidinyl-1H-1,2,4-triazol-3-sulfonsäureamide, Verfahren zu ihrer Herstellung und ihre Verwendung als Mittel mit herbizider Wirkung
GB2136427A (en)	1984-09-19	Herbicidal N-pyridylpyrazole Derivatives
US4629495A (en)	1986-12-16	Herbicidal 5-amino-4-cyano-1-phenylpyrazoles
EP0243136A2 (en)	1987-10-28	Anilinopyrimidine fungicides
JP4580171B2 (ja)	2010-11-10	３−フェノキシ−４−ピリダジノール誘導体を含有する除草性組成物
US4505740A (en)	1985-03-19	Herbicidal 5-amino-4-cyano-1-phenyl-pyrazoles
US5186736A (en)	1993-02-16	Heterocyclic N-acylsulfonamides and their use as herbicides or growth regulators
IE893138L (en)	1990-04-04	Sulphonamides
US6232271B1 (en)	2001-05-15	1-Methyl-5-alkylsulfonyl-, 1-methyl-5-alkylsulfinyl- and 1-methyl-5-alkylthio- substituted pyrazolylpyrazoles, processes for their preparation and their use as herbicides
CN114163430A (zh)	2022-03-11	一种苯并噻二嗪衍生物及其在农业中的应用
WO2001068613A1 (en)	2001-09-20	Pyrimidinone derivatives and herbicides
EP0596109B1 (en)	1996-12-18	Sulfamidosulfonamide derivatives and herbicides
EP0461797A1 (en)	1991-12-18	Herbicidal oximethers
DE3408727A1 (de)	1984-09-13	N-pyridylpyrazolderivate, ihre herstellung und ihre verwendung als herbicide
JP3378237B2 (ja)	2003-02-17	殺虫性ジヒドロ−オキサジアジン類、−チアジアジン類および−トリアジン類
EP0397295A2 (de)	1990-11-14	2-Phenyl-perhydro-isoindol-1-one und -1-thione, Verfahren zu ihrer Herstellung und ihre Verwendung als Mittel mit herbizider Wirkung
CA2043704A1 (en)	1991-12-15	Compounds