CA1129861A - Derives d'uree, et compositions insictides contenant des derives - Google Patents

Derives d'uree, et compositions insictides contenant des derives

Info

Publication number: CA1129861A
Authority: CA; Canada
Prior art keywords: halo; methyl; alkyl; compound; urea
Prior art date: 1977-06-22
Legal status (The legal status 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 status listed.): Expired

Application number

CA305,703A

Other languages

English (en)

Inventor

John L. Miesel

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Eli Lilly and Co

Original Assignee

Eli Lilly and Co

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.)

1977-06-22

Filing date

1978-06-19

Publication date

1982-08-17

1978-06-19 Application filed by Eli Lilly and Co filed Critical Eli Lilly and Co

1982-08-17 Application granted granted Critical

1982-08-17 Publication of CA1129861A publication Critical patent/CA1129861A/fr

Status Expired legal-status Critical Current

Links

230000000749 insecticidal effect Effects 0.000 title claims description 19
150000003672 ureas Chemical class 0.000 title abstract description 7
239000000203 mixture Substances 0.000 title description 73
150000001875 compounds Chemical class 0.000 claims abstract description 121
-1 2-substituted-benzoyl compound Chemical class 0.000 claims abstract description 44
239000002917 insecticide Substances 0.000 claims abstract description 9
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 50
125000005843 halogen group Chemical group 0.000 claims description 50
238000000034 method Methods 0.000 claims description 41
239000001257 hydrogen Substances 0.000 claims description 31
229910052739 hydrogen Inorganic materials 0.000 claims description 31
239000004202 carbamide Substances 0.000 claims description 28
125000004307 pyrazin-2-yl group Chemical group [H]C1=C([H])N=C(*)C([H])=N1 0.000 claims description 28
241000238631 Hexapoda Species 0.000 claims description 25
150000002431 hydrogen Chemical group 0.000 claims description 23
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 19
125000000217 alkyl group Chemical group 0.000 claims description 17
125000001246 bromo group Chemical group Br* 0.000 claims description 13
125000001309 chloro group Chemical group Cl* 0.000 claims description 13
125000003545 alkoxy group Chemical group 0.000 claims description 10
125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 9
125000004093 cyano group Chemical group *C#N 0.000 claims description 7
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 7
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 7
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
125000004414 alkyl thio group Chemical group 0.000 claims description 6
239000000463 material Substances 0.000 claims description 5
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 5
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 4
125000001624 naphthyl group Chemical group 0.000 claims description 4
FBTIDAZYXBHHHU-UHFFFAOYSA-N 2-bromo-n-[[5-(4-bromophenyl)-6-methylpyrazin-2-yl]carbamoyl]benzamide Chemical compound C=1N=C(C=2C=CC(Br)=CC=2)C(C)=NC=1NC(=O)NC(=O)C1=CC=CC=C1Br FBTIDAZYXBHHHU-UHFFFAOYSA-N 0.000 claims description 2
ALFCDCZODNAGJC-UHFFFAOYSA-N 2-chloro-n-[(5-cyclohexyl-6-methylpyrazin-2-yl)carbamoyl]benzamide Chemical compound C=1N=C(C2CCCCC2)C(C)=NC=1NC(=O)NC(=O)C1=CC=CC=C1Cl ALFCDCZODNAGJC-UHFFFAOYSA-N 0.000 claims description 2
GZKFVNMIQZIJDT-UHFFFAOYSA-N 2-chloro-n-[[5-(4-chlorophenyl)-6-methylpyrazin-2-yl]carbamoyl]benzamide Chemical compound C=1N=C(C=2C=CC(Cl)=CC=2)C(C)=NC=1NC(=O)NC(=O)C1=CC=CC=C1Cl GZKFVNMIQZIJDT-UHFFFAOYSA-N 0.000 claims description 2
XBBHLEGAPJISKM-UHFFFAOYSA-N 2-chloro-n-[[5-(4-ethylphenyl)-6-methylpyrazin-2-yl]carbamoyl]benzamide Chemical compound C1=CC(CC)=CC=C1C(C(=N1)C)=NC=C1NC(=O)NC(=O)C1=CC=CC=C1Cl XBBHLEGAPJISKM-UHFFFAOYSA-N 0.000 claims description 2
HJKDYRWBLAXCGF-UHFFFAOYSA-N 2-chloro-n-[[5-(4-fluorophenyl)-6-methylpyrazin-2-yl]carbamoyl]benzamide Chemical compound C=1N=C(C=2C=CC(F)=CC=2)C(C)=NC=1NC(=O)NC(=O)C1=CC=CC=C1Cl HJKDYRWBLAXCGF-UHFFFAOYSA-N 0.000 claims description 2
ICCGHDMSTTZRLM-UHFFFAOYSA-N 2-chloro-n-[[5-(4-methoxyphenyl)-6-methylpyrazin-2-yl]carbamoyl]benzamide Chemical compound C1=CC(OC)=CC=C1C(C(=N1)C)=NC=C1NC(=O)NC(=O)C1=CC=CC=C1Cl ICCGHDMSTTZRLM-UHFFFAOYSA-N 0.000 claims description 2
RYYIXOAYZYKJDP-UHFFFAOYSA-N 2-chloro-n-[[6-methyl-5-(4-methylsulfanylphenyl)pyrazin-2-yl]carbamoyl]benzamide Chemical compound C1=CC(SC)=CC=C1C(C(=N1)C)=NC=C1NC(=O)NC(=O)C1=CC=CC=C1Cl RYYIXOAYZYKJDP-UHFFFAOYSA-N 0.000 claims description 2
125000006526 (C1-C2) alkyl group Chemical group 0.000 claims 9
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 6
125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 3
125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 3
125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 claims 2
125000004435 hydrogen atom Chemical group [H]* 0.000 claims 2
125000004491 isohexyl group Chemical group C(CCC(C)C)* 0.000 claims 2
125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims 1
OCACPNJQALDFKE-UHFFFAOYSA-N n-[[5-(4-bromophenyl)-6-methylpyrazin-2-yl]carbamoyl]-2-chlorobenzamide Chemical compound C=1N=C(C=2C=CC(Br)=CC=2)C(C)=NC=1NC(=O)NC(=O)C1=CC=CC=C1Cl OCACPNJQALDFKE-UHFFFAOYSA-N 0.000 claims 1
235000013877 carbamide Nutrition 0.000 abstract description 29
125000003373 pyrazinyl group Chemical group 0.000 abstract description 3
238000002844 melting Methods 0.000 description 45
230000008018 melting Effects 0.000 description 45
239000007787 solid Substances 0.000 description 43
KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Natural products C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 38
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 33
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 27
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 27
ZTUIVBFRTPPWEZ-UHFFFAOYSA-N 2-chlorobenzoyl isocyanate Chemical compound ClC1=CC=CC=C1C(=O)N=C=O ZTUIVBFRTPPWEZ-UHFFFAOYSA-N 0.000 description 26
238000002360 preparation method Methods 0.000 description 26
238000012360 testing method Methods 0.000 description 25
238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 22
239000000243 solution Substances 0.000 description 22
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 21
239000002904 solvent Substances 0.000 description 21
PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 description 20
238000005303 weighing Methods 0.000 description 20
239000000543 intermediate Substances 0.000 description 19
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 18
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 18
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 16
239000000047 product Substances 0.000 description 16
238000002329 infrared spectrum Methods 0.000 description 15
239000011541 reaction mixture Substances 0.000 description 15
241000196324 Embryophyta Species 0.000 description 14
238000006243 chemical reaction Methods 0.000 description 14
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 13
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 12
238000000921 elemental analysis Methods 0.000 description 12
238000002474 experimental method Methods 0.000 description 12
241001521235 Spodoptera eridania Species 0.000 description 10
238000009472 formulation Methods 0.000 description 10
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
239000007795 chemical reaction product Substances 0.000 description 9
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 8
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 8
239000003921 oil Substances 0.000 description 8
150000002923 oximes Chemical class 0.000 description 8
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 7
244000068988 Glycine max Species 0.000 description 7
238000004458 analytical method Methods 0.000 description 7
239000012876 carrier material Substances 0.000 description 7
239000000706 filtrate Substances 0.000 description 7
239000007858 starting material Substances 0.000 description 7
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 7
SJYCYRJOUJAQFB-UHFFFAOYSA-N 5-(4-bromophenyl)-6-methylpyrazin-2-amine Chemical compound CC1=NC(N)=CN=C1C1=CC=C(Br)C=C1 SJYCYRJOUJAQFB-UHFFFAOYSA-N 0.000 description 6
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
244000046052 Phaseolus vulgaris Species 0.000 description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 6
238000003756 stirring Methods 0.000 description 6
239000012085 test solution Substances 0.000 description 6
CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 6
241000254173 Coleoptera Species 0.000 description 5
241000255925 Diptera Species 0.000 description 5
241000462639 Epilachna varivestis Species 0.000 description 5
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 5
241001477931 Mythimna unipuncta Species 0.000 description 5
229960000583 acetic acid Drugs 0.000 description 5
239000000460 chlorine Substances 0.000 description 5
235000013601 eggs Nutrition 0.000 description 5
125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 5
238000011282 treatment Methods 0.000 description 5
125000003541 2-chlorobenzoyl group Chemical group ClC1=C(C(=O)*)C=CC=C1 0.000 description 4
RZMVHCYCUAKRMM-UHFFFAOYSA-N 2-methylbenzoyl isocyanate Chemical compound CC1=CC=CC=C1C(=O)N=C=O RZMVHCYCUAKRMM-UHFFFAOYSA-N 0.000 description 4
NHUFIOMPICRXFX-UHFFFAOYSA-N 5,6-dichloropyrazin-2-amine Chemical compound NC1=CN=C(Cl)C(Cl)=N1 NHUFIOMPICRXFX-UHFFFAOYSA-N 0.000 description 4
HWCKAMAVEWVBDO-UHFFFAOYSA-N 5-chloropyrazin-2-amine Chemical compound NC1=CN=C(Cl)C=N1 HWCKAMAVEWVBDO-UHFFFAOYSA-N 0.000 description 4
241000256118 Aedes aegypti Species 0.000 description 4
235000010469 Glycine max Nutrition 0.000 description 4
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
JRNVZBWKYDBUCA-UHFFFAOYSA-N N-chlorosuccinimide Chemical compound ClN1C(=O)CCC1=O JRNVZBWKYDBUCA-UHFFFAOYSA-N 0.000 description 4
239000004480 active ingredient Substances 0.000 description 4
230000000875 corresponding effect Effects 0.000 description 4
238000011156 evaluation Methods 0.000 description 4
239000000284 extract Substances 0.000 description 4
239000008187 granular material Substances 0.000 description 4
JGAJCAJHSHUPGH-UHFFFAOYSA-N methyl 3-amino-6-chloropyrazine-2-carboxylate Chemical compound COC(=O)C1=NC(Cl)=CN=C1N JGAJCAJHSHUPGH-UHFFFAOYSA-N 0.000 description 4
238000002156 mixing Methods 0.000 description 4
230000003151 ovacidal effect Effects 0.000 description 4
239000002244 precipitate Substances 0.000 description 4
238000000746 purification Methods 0.000 description 4
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 4
SLCZNGZFOVAAED-UHFFFAOYSA-N 2-aminoethanimidamide;dihydrobromide Chemical compound Br.Br.NCC(N)=N SLCZNGZFOVAAED-UHFFFAOYSA-N 0.000 description 3
TZEPSUWOCPVNMM-UHFFFAOYSA-N 3-amino-6-chloropyrazine-2-carboxylic acid Chemical compound NC1=NC=C(Cl)N=C1C(O)=O TZEPSUWOCPVNMM-UHFFFAOYSA-N 0.000 description 3
ILDRNIDSVAZBMZ-UHFFFAOYSA-N 5-(trifluoromethyl)pyrazin-2-amine Chemical compound NC1=CN=C(C(F)(F)F)C=N1 ILDRNIDSVAZBMZ-UHFFFAOYSA-N 0.000 description 3
NFFWTXKHMBVZFK-UHFFFAOYSA-N 6-methyl-5-phenylpyrazin-2-amine Chemical compound CC1=NC(N)=CN=C1C1=CC=CC=C1 NFFWTXKHMBVZFK-UHFFFAOYSA-N 0.000 description 3
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 3
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 3
241000255777 Lepidoptera Species 0.000 description 3
241000238814 Orthoptera Species 0.000 description 3
235000010627 Phaseolus vulgaris Nutrition 0.000 description 3
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
239000000443 aerosol Substances 0.000 description 3
125000004390 alkyl sulfonyl group Chemical group 0.000 description 3
239000002274 desiccant Substances 0.000 description 3
235000014113 dietary fatty acids Nutrition 0.000 description 3
230000000694 effects Effects 0.000 description 3
239000000194 fatty acid Substances 0.000 description 3
229930195729 fatty acid Natural products 0.000 description 3
150000004665 fatty acids Chemical class 0.000 description 3
150000002576 ketones Chemical class 0.000 description 3
230000001418 larval effect Effects 0.000 description 3
239000007788 liquid Substances 0.000 description 3
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 3
125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 3
239000004033 plastic Substances 0.000 description 3
150000003216 pyrazines Chemical class 0.000 description 3
230000009885 systemic effect Effects 0.000 description 3
125000005490 tosylate group Chemical class 0.000 description 3
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
JVSDZAGCHKCSGR-UHFFFAOYSA-N 2,5-dichloropyrazine Chemical compound ClC1=CN=C(Cl)C=N1 JVSDZAGCHKCSGR-UHFFFAOYSA-N 0.000 description 2
YQFMCAINTRXXKR-UHFFFAOYSA-N 2-(benzenesulfinyl)-5-chloropyrazine Chemical compound C1=NC(Cl)=CN=C1S(=O)C1=CC=CC=C1 YQFMCAINTRXXKR-UHFFFAOYSA-N 0.000 description 2
TVLWOUSLEZPYDQ-UHFFFAOYSA-N 2-(benzenesulfonyl)-5-chloropyrazine Chemical compound C1=NC(Cl)=CN=C1S(=O)(=O)C1=CC=CC=C1 TVLWOUSLEZPYDQ-UHFFFAOYSA-N 0.000 description 2
GOJUJUVQIVIZAV-UHFFFAOYSA-N 2-amino-4,6-dichloropyrimidine-5-carbaldehyde Chemical group NC1=NC(Cl)=C(C=O)C(Cl)=N1 GOJUJUVQIVIZAV-UHFFFAOYSA-N 0.000 description 2
JTPXVCKCLBROOJ-UHFFFAOYSA-N 2-amino-6-chloropyrazine Chemical compound NC1=CN=CC(Cl)=N1 JTPXVCKCLBROOJ-UHFFFAOYSA-N 0.000 description 2
MEUWQVWJLLBVQI-UHFFFAOYSA-N 2-aminopropanedinitrile;4-methylbenzenesulfonic acid Chemical compound N#CC([NH3+])C#N.CC1=CC=C(S([O-])(=O)=O)C=C1 MEUWQVWJLLBVQI-UHFFFAOYSA-N 0.000 description 2
WGFILESHIVMXAY-UHFFFAOYSA-N 2-bromobenzoyl isocyanate Chemical compound BrC1=CC=CC=C1C(=O)N=C=O WGFILESHIVMXAY-UHFFFAOYSA-N 0.000 description 2
125000005999 2-bromoethyl group Chemical group 0.000 description 2
VURJRDMNQZNCPM-UHFFFAOYSA-N 2-chloro-n-[[5-(trifluoromethyl)pyrazin-2-yl]carbamoyl]benzamide Chemical compound C1=NC(C(F)(F)F)=CN=C1NC(=O)NC(=O)C1=CC=CC=C1Cl VURJRDMNQZNCPM-UHFFFAOYSA-N 0.000 description 2
RBGDLYUEXLWQBZ-UHFFFAOYSA-N 2-chlorobenzamide Chemical compound NC(=O)C1=CC=CC=C1Cl RBGDLYUEXLWQBZ-UHFFFAOYSA-N 0.000 description 2
PSKYXWMZYBYVDK-UHFFFAOYSA-N 3,3,3-trifluoro-1-phenylpropane-1,2-dione;hydrate Chemical compound O.FC(F)(F)C(=O)C(=O)C1=CC=CC=C1 PSKYXWMZYBYVDK-UHFFFAOYSA-N 0.000 description 2
NRDPLJROSGVEDO-UHFFFAOYSA-N 3,5,6-trichloropyrazin-2-amine Chemical compound NC1=NC(Cl)=C(Cl)N=C1Cl NRDPLJROSGVEDO-UHFFFAOYSA-N 0.000 description 2
CJXBBQKTUJXSGF-UHFFFAOYSA-N 3,6-dichloropyrazin-2-amine Chemical compound NC1=NC(Cl)=CN=C1Cl CJXBBQKTUJXSGF-UHFFFAOYSA-N 0.000 description 2
AUWYVCBOBIRRGR-UHFFFAOYSA-N 4-bromo-1-phenylbutan-1-one Chemical compound BrCCCC(=O)C1=CC=CC=C1 AUWYVCBOBIRRGR-UHFFFAOYSA-N 0.000 description 2
QYCWZGDAYYKQTL-UHFFFAOYSA-N 5-(4-bromophenyl)-6-ethylpyrazin-2-amine Chemical compound CCC1=NC(N)=CN=C1C1=CC=C(Br)C=C1 QYCWZGDAYYKQTL-UHFFFAOYSA-N 0.000 description 2
LGVCMQGHHBAYBA-UHFFFAOYSA-N 5-(4-chlorophenyl)pyrazin-2-amine Chemical compound C1=NC(N)=CN=C1C1=CC=C(Cl)C=C1 LGVCMQGHHBAYBA-UHFFFAOYSA-N 0.000 description 2
CVJPYKAULVWKBH-UHFFFAOYSA-N 5-(4-methoxyphenyl)-6-methylpyrazin-2-amine Chemical compound C1=CC(OC)=CC=C1C1=NC=C(N)N=C1C CVJPYKAULVWKBH-UHFFFAOYSA-N 0.000 description 2
BBGAQYOMHGXLGG-UHFFFAOYSA-N 5-cyclohexyl-6-methylpyrazin-2-amine Chemical compound CC1=NC(N)=CN=C1C1CCCCC1 BBGAQYOMHGXLGG-UHFFFAOYSA-N 0.000 description 2
UMKXTWMATLULJT-UHFFFAOYSA-N 5-phenyl-6-(trifluoromethyl)pyrazin-2-amine Chemical compound FC(F)(F)C1=NC(N)=CN=C1C1=CC=CC=C1 UMKXTWMATLULJT-UHFFFAOYSA-N 0.000 description 2
KJAKXVBZQBPPOB-UHFFFAOYSA-N 5-phenylpyrazin-2-amine Chemical compound C1=NC(N)=CN=C1C1=CC=CC=C1 KJAKXVBZQBPPOB-UHFFFAOYSA-N 0.000 description 2
FMBKXKZEXQCCFM-UHFFFAOYSA-N 6-(trifluoromethyl)pyrazin-2-amine Chemical compound NC1=CN=CC(C(F)(F)F)=N1 FMBKXKZEXQCCFM-UHFFFAOYSA-N 0.000 description 2
QBPBGMNPWCHVGO-UHFFFAOYSA-N 6-methyl-5-(4-methylsulfanylphenyl)pyrazin-2-amine Chemical compound C1=CC(SC)=CC=C1C1=NC=C(N)N=C1C QBPBGMNPWCHVGO-UHFFFAOYSA-N 0.000 description 2
KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
240000003259 Brassica oleracea var. botrytis Species 0.000 description 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 2
ZAKOWWREFLAJOT-CEFNRUSXSA-N D-alpha-tocopherylacetate Chemical compound CC(=O)OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C ZAKOWWREFLAJOT-CEFNRUSXSA-N 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
241001301805 Epilachna Species 0.000 description 2
240000000047 Gossypium barbadense Species 0.000 description 2
235000009429 Gossypium barbadense Nutrition 0.000 description 2
241000255967 Helicoverpa zea Species 0.000 description 2
241000258937 Hemiptera Species 0.000 description 2
241001508566 Hypera postica Species 0.000 description 2
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
241001012098 Omiodes indicata Species 0.000 description 2
KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 description 2
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
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239000007864 aqueous solution Substances 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
239000011324 bead Substances 0.000 description 1
239000000440 bentonite Substances 0.000 description 1
229910000278 bentonite Inorganic materials 0.000 description 1
SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
229940054066 benzamide antipsychotics Drugs 0.000 description 1
KXDAEFPNCMNJSK-UHFFFAOYSA-N benzene carboxamide Natural products NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 description 1
125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 1
LURYMYITPCOQAU-UHFFFAOYSA-N benzoyl isocyanate Chemical class O=C=NC(=O)C1=CC=CC=C1 LURYMYITPCOQAU-UHFFFAOYSA-N 0.000 description 1
150000008047 benzoylureas Chemical class 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
239000004305 biphenyl Substances 0.000 description 1
125000004799 bromophenyl group Chemical group 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
239000000969 carrier Substances 0.000 description 1
235000013339 cereals Nutrition 0.000 description 1
239000002026 chloroform extract Substances 0.000 description 1
238000004587 chromatography analysis Methods 0.000 description 1
239000004927 clay Substances 0.000 description 1
238000004440 column chromatography Methods 0.000 description 1
229940125904 compound 1 Drugs 0.000 description 1
229940125782 compound 2 Drugs 0.000 description 1
229940126214 compound 3 Drugs 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
235000005822 corn Nutrition 0.000 description 1
239000013058 crude material Substances 0.000 description 1
239000002178 crystalline material Substances 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
230000001419 dependent effect Effects 0.000 description 1
238000011161 development Methods 0.000 description 1
230000018109 developmental process Effects 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
229940116441 divinylbenzene Drugs 0.000 description 1
MYRTYDVEIRVNKP-UHFFFAOYSA-N divinylbenzene Substances C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 1
239000010459 dolomite Substances 0.000 description 1
229910000514 dolomite Inorganic materials 0.000 description 1
239000003814 drug Substances 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
239000012259 ether extract Substances 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
JYGRVMQGWVVHJE-UHFFFAOYSA-N ethyl 2-amino-2-cyanoacetate Chemical compound CCOC(=O)C(N)C#N JYGRVMQGWVVHJE-UHFFFAOYSA-N 0.000 description 1
XTWPKWKHIDZUNZ-UHFFFAOYSA-N ethyl 3-amino-6-(4-bromophenyl)-5-chloropyrazine-2-carboxylate Chemical compound N1=C(N)C(C(=O)OCC)=NC(C=2C=CC(Br)=CC=2)=C1Cl XTWPKWKHIDZUNZ-UHFFFAOYSA-N 0.000 description 1
125000006125 ethylsulfonyl group Chemical group 0.000 description 1
125000004705 ethylthio group Chemical group C(C)S* 0.000 description 1
239000002657 fibrous material Substances 0.000 description 1
238000001914 filtration Methods 0.000 description 1
125000001153 fluoro group Chemical group F* 0.000 description 1
NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 1
239000011521 glass Substances 0.000 description 1
239000010440 gypsum Substances 0.000 description 1
229910052602 gypsum Inorganic materials 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
238000003898 horticulture Methods 0.000 description 1
125000001841 imino group Chemical group [H]N=* 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
230000002452 interceptive effect Effects 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
125000002510 isobutoxy group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])O* 0.000 description 1
IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate Chemical compound [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
230000029052 metamorphosis Effects 0.000 description 1
125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 1
125000006216 methylsulfinyl group Chemical group [H]C([H])([H])S(*)=O 0.000 description 1
125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 description 1
239000011707 mineral Substances 0.000 description 1
235000010755 mineral Nutrition 0.000 description 1
OGLABTBQSITZSQ-UHFFFAOYSA-N n-[[5-(4-bromophenyl)-6-chloropyrazin-2-yl]carbamoyl]-2-chlorobenzamide Chemical compound ClC1=CC=CC=C1C(=O)NC(=O)NC1=CN=C(C=2C=CC(Br)=CC=2)C(Cl)=N1 OGLABTBQSITZSQ-UHFFFAOYSA-N 0.000 description 1
125000006093 n-propyl sulfinyl group Chemical group 0.000 description 1
125000006124 n-propyl sulfonyl group Chemical group 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
231100000194 ovacidal Toxicity 0.000 description 1
239000007800 oxidant agent Substances 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
ZJVAWPKTWVFKHG-UHFFFAOYSA-N p-Methoxypropiophenone Chemical compound CCC(=O)C1=CC=C(OC)C=C1 ZJVAWPKTWVFKHG-UHFFFAOYSA-N 0.000 description 1
125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
230000000361 pesticidal effect Effects 0.000 description 1
239000003209 petroleum derivative Substances 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-M phenolate Chemical compound [O-]C1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-M 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
239000003380 propellant Substances 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000008262 pumice Substances 0.000 description 1
XFTQRUTUGRCSGO-UHFFFAOYSA-N pyrazin-2-amine Chemical compound NC1=CN=CC=N1 XFTQRUTUGRCSGO-UHFFFAOYSA-N 0.000 description 1
NIPZZXUFJPQHNH-UHFFFAOYSA-N pyrazine-2-carboxylic acid Chemical compound OC(=O)C1=CN=CC=N1 NIPZZXUFJPQHNH-UHFFFAOYSA-N 0.000 description 1
IPEHBUMCGVEMRF-UHFFFAOYSA-N pyrazinecarboxamide Chemical compound NC(=O)C1=CN=CC=N1 IPEHBUMCGVEMRF-UHFFFAOYSA-N 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
238000010992 reflux Methods 0.000 description 1
239000004576 sand Substances 0.000 description 1
238000013207 serial dilution Methods 0.000 description 1
239000000741 silica gel Substances 0.000 description 1
229910002027 silica gel Inorganic materials 0.000 description 1
239000001632 sodium acetate Substances 0.000 description 1
235000017281 sodium acetate Nutrition 0.000 description 1
235000017557 sodium bicarbonate Nutrition 0.000 description 1
229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
235000010265 sodium sulphite Nutrition 0.000 description 1
239000011343 solid material Substances 0.000 description 1
239000012265 solid product Substances 0.000 description 1
241000894007 species Species 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
239000002641 tar oil Substances 0.000 description 1
239000004557 technical material Substances 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1
230000000007 visual effect Effects 0.000 description 1
235000020234 walnut Nutrition 0.000 description 1
230000036642 wellbeing Effects 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
239000008096 xylene Substances 0.000 description 1
125000005023 xylyl group Chemical group 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
- C07D241/10—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D241/14—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having 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
- C07D241/24—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- 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<
- A01N47/34—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the groups, e.g. biuret; Thio analogues thereof; Urea-aldehyde condensation products
- 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<
- A01N47/36—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C275/46—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups containing any of the groups, X being a hetero atom, Y being any atom, e.g. acylureas
- C07C275/48—Y being a hydrogen or a carbon atom
- C07C275/54—Y being a carbon atom of a six-membered aromatic ring, e.g. benzoylureas
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
- C07D241/10—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D241/14—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having 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
- C07D241/20—Nitrogen atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
- C07D241/10—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D241/14—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having 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
- C07D241/24—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D241/26—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with nitrogen atoms directly attached to ring carbon atoms

Landscapes

Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
Plant Pathology (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Plural Heterocyclic Compounds (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

CA305,703A 1977-06-22 1978-06-19 Derives d'uree, et compositions insictides contenant des derives Expired CA1129861A (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
GB2609377		1977-06-22
GB26093/77		1977-06-22

Publications (1)

Publication Number	Publication Date
CA1129861A true CA1129861A (fr)	1982-08-17

Family

ID=10238257

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA305,703A Expired CA1129861A (fr)	1977-06-22	1978-06-19	Derives d'uree, et compositions insictides contenant des derives

Country Status (11)

Country	Link
BE (1)	BE868228A (fr)
CA (1)	CA1129861A (fr)
CS (1)	CS198104B2 (fr)
DD (1)	DD143721A5 (fr)
ES (1)	ES471057A1 (fr)
FR (1)	FR2398739A1 (fr)
GB (1)	GB2066806B (fr)
HU (1)	HU185336B (fr)
IN (1)	IN149912B (fr)
SE (1)	SE8303206D0 (fr)
ZA (1)	ZA783553B (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4212870A (en) *	1979-06-18	1980-07-15	Gulf Oil Corporation	1-(2,6-Dichlorobenzoyl)-3-(5-chloro-2-pyridinyl-N-oxide)urea and use as insecticide
EP2878198B1 (fr)	2013-11-29	2016-09-14	Flügel GmbH	Procédé destiné à attirer des insectes cambiophages, xylophages et/ou mycétophages

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EG11837A (en) *	1974-09-19	1977-12-31	Lilly Co Eli	Novel 1-(substituted benzoyl)-3-(substituted pyrazinyl ureas used as insecticides

1978
- 1978-06-16 IN IN666/CAL/78A patent/IN149912B/en unknown
- 1978-06-19 BE BE1008936A patent/BE868228A/fr not_active IP Right Cessation
- 1978-06-19 GB GB8019107A patent/GB2066806B/en not_active Expired
- 1978-06-19 CA CA305,703A patent/CA1129861A/fr not_active Expired
- 1978-06-20 HU HU821470A patent/HU185336B/hu unknown
- 1978-06-21 CS CS784095A patent/CS198104B2/cs unknown
- 1978-06-21 ZA ZA783553A patent/ZA783553B/xx unknown
- 1978-06-22 DD DD78213690A patent/DD143721A5/de unknown
- 1978-06-22 ES ES471057A patent/ES471057A1/es not_active Expired
- 1978-11-17 FR FR7832550A patent/FR2398739A1/fr active Granted
1983
- 1983-06-07 SE SE8303206A patent/SE8303206D0/xx not_active Application Discontinuation

Also Published As

Publication number	Publication date
BE868228A (fr)	1978-12-19
SE8303206L (sv)	1983-06-07
GB2066806B (en)	1982-08-18
ES471057A1 (es)	1980-01-16
IN149912B (fr)	1982-05-29
HU185336B (en)	1985-01-28
DD143721A5 (de)	1980-09-10
GB2066806A (en)	1981-07-15
FR2398739A1 (fr)	1979-02-23
ZA783553B (en)	1980-02-27
SE8303206D0 (sv)	1983-06-07
FR2398739B1 (fr)	1982-11-05
CS198104B2 (en)	1980-05-30

Legal Events

Date	Code	Title	Description
1999-08-17	MKEX	Expiry

Publication	Publication Date	Title
JP2639423B2 (ja)	1997-08-13	置換されたグアニジン類、その製法及び有害生物防除のための該化合物の使用法
CA1292231C (fr)	1991-11-19	Pyrimidines substituees
US4293552A (en)	1981-10-06	Novel 1-(mono-o-substituted benzoyl)-3-(substituted pyrazinyl) ureas
US4160834A (en)	1979-07-10	1-(Substituted benzoyl)-3-(substituted pyrazinyl)ureas
US4083977A (en)	1978-04-11	Novel insecticidal 1-(substituted benzoyl)-3-(substituted pyrazinyl)ureas
DE2726684A1 (de)	1979-01-04	Insektizide mittel
EP0246061B1 (fr)	1992-03-18	Dérivés de benzoylurée ; préparation et utilisation
EP0124282B1 (fr)	1987-09-30	Bicyclo-oxyaryl-thiourées et procédé de préparation
AU595303B2 (en)	1990-03-29	Six-membered n-heterocyclic derivatives of n'-substituted-n, n'-diacylhydrazines
US4696938A (en)	1987-09-29	Insecticidal 6-aryl-pyridine thiosemicarbazones
EP0098158A1 (fr)	1984-01-11	1-(Alkylphénoxyaryl)-3-benzoylurées à activité pesticide et procédé pour leur préparation
JPH0617357B2 (ja)	1994-03-09	新規なベンゾイル尿素化合物、その製造方法およびベンゾイル尿素化合物を含有する殺虫・殺ダニ剤組成物
KR910004359B1 (ko)	1991-06-26	벤조일우레아 유도체의 제조방법
US4521426A (en)	1985-06-04	Pesticidal bicyclooxyheterocyclyl aroyl ureas
US4318924A (en)	1982-03-09	Combating bacteria with N-cycloalkyl-N'-substituted-N'-acyl-ureas
GB2066806A (en)	1981-07-15	Novel 1-(mono-o-substituted Benzoyl)-3-(substituted Pyrazinyl)Ureas and Their Preparation
US4366155A (en)	1982-12-28	1-Benzoyl-3-(6-oxopyridazinyl)ureas, compositions, and insecticidal method
HU182954B (en)	1984-03-28	Process for producing 1-bracket-2,6-dihalogeno-benzoyl-bracket closed-3-bracket-2-pyridinyl-bracket closedurea derivatives, and insecticide compositions containing them as active agents
EP0232080B1 (fr)	1990-05-16	Benzoylurées, leur préparation et utilisation
KR820000545B1 (ko)	1982-04-13	우레아 유도체의 제조방법
CH638500A5 (de)	1983-09-30	1-(mono-o-substituierte-benzoyl)-3-(substituierte-pyrazinyl)-harnstoffe sowie diese verbindungen enthaltende insektizide.
US4357347A (en)	1982-11-02	Pesticidal phenylcarbamoylbenzimidates
US3839564A (en)	1974-10-01	Insecticidal compositions and methods of killing insects using alpha,beta-dioxohydrocinnamonitriles
CA1293516C (fr)	1991-12-24	Derive benzoyluree, sa production et son utilisation
EP0115210A1 (fr)	1984-08-08	Benzoyl uréas à activité pesticide et procédé pour leur préparation