CH631603A5 - Insecticide - Google Patents
Insecticide Download PDFInfo
- Publication number
- CH631603A5 CH631603A5 CH146977A CH146977A CH631603A5 CH 631603 A5 CH631603 A5 CH 631603A5 CH 146977 A CH146977 A CH 146977A CH 146977 A CH146977 A CH 146977A CH 631603 A5 CH631603 A5 CH 631603A5
- Authority
- CH
- Switzerland
- Prior art keywords
- hydrogen
- radicals
- chlorine
- bromine
- thiadiazol
- Prior art date
Links
- 239000002917 insecticide Substances 0.000 title claims description 11
- 150000001875 compounds Chemical class 0.000 claims description 97
- 229910052739 hydrogen Inorganic materials 0.000 claims description 67
- 239000001257 hydrogen Substances 0.000 claims description 64
- -1 acetamido, methoxy, nitro, amino Chemical group 0.000 claims description 61
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 54
- 239000000460 chlorine Substances 0.000 claims description 54
- 229910052801 chlorine Inorganic materials 0.000 claims description 54
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 53
- 229910052794 bromium Inorganic materials 0.000 claims description 53
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 52
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 39
- 229910052731 fluorine Inorganic materials 0.000 claims description 39
- 239000011737 fluorine Substances 0.000 claims description 39
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 36
- 239000000203 mixture Substances 0.000 claims description 33
- 150000002431 hydrogen Chemical class 0.000 claims description 31
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 30
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 29
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 28
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 27
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 22
- 125000004076 pyridyl group Chemical group 0.000 claims description 16
- 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 claims description 14
- 125000000842 isoxazolyl group Chemical group 0.000 claims description 14
- 125000001544 thienyl group Chemical group 0.000 claims description 14
- 125000002541 furyl group Chemical group 0.000 claims description 13
- 125000005493 quinolyl group Chemical group 0.000 claims description 13
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 claims description 12
- 125000004618 benzofuryl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 claims description 9
- 229910052736 halogen Inorganic materials 0.000 claims description 9
- 150000002367 halogens Chemical class 0.000 claims description 9
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 9
- 125000001624 naphthyl group Chemical group 0.000 claims description 8
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 claims description 7
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 6
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 6
- 229910052760 oxygen Inorganic materials 0.000 claims description 6
- 239000001301 oxygen Substances 0.000 claims description 6
- CHAYRXZJAZXJRB-UHFFFAOYSA-N n-[5-(4-chlorophenyl)-1,3,4-thiadiazol-2-yl]-2,6-dimethoxybenzamide Chemical compound COC1=CC=CC(OC)=C1C(=O)NC1=NN=C(C=2C=CC(Cl)=CC=2)S1 CHAYRXZJAZXJRB-UHFFFAOYSA-N 0.000 claims description 5
- 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 claims description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 4
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 4
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- 229910052717 sulfur Chemical group 0.000 claims description 4
- 239000011593 sulfur Chemical group 0.000 claims description 4
- MNOULQLXILYKNV-UHFFFAOYSA-N 5-[4-(trifluoromethyl)phenyl]-1h-pyrazole Chemical compound C1=CC(C(F)(F)F)=CC=C1C1=CC=NN1 MNOULQLXILYKNV-UHFFFAOYSA-N 0.000 claims description 3
- IITOCTXMJQVOIO-UHFFFAOYSA-N 2,6-dimethoxy-n-[5-[3-(trifluoromethyl)phenyl]-1,3,4-thiadiazol-2-yl]benzamide Chemical compound COC1=CC=CC(OC)=C1C(=O)NC1=NN=C(C=2C=C(C=CC=2)C(F)(F)F)S1 IITOCTXMJQVOIO-UHFFFAOYSA-N 0.000 claims description 2
- NXDXMSTXCYCUGG-UHFFFAOYSA-N 2,6-dimethylbenzamide Chemical compound CC1=CC=CC(C)=C1C(N)=O NXDXMSTXCYCUGG-UHFFFAOYSA-N 0.000 claims description 2
- 125000001207 fluorophenyl group Chemical group 0.000 claims description 2
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims description 2
- MNWSGMTUGXNYHJ-UHFFFAOYSA-N 2-methoxybenzamide Chemical compound COC1=CC=CC=C1C(N)=O MNWSGMTUGXNYHJ-UHFFFAOYSA-N 0.000 claims 1
- 102100041023 Coronin-2A Human genes 0.000 claims 1
- 101000748858 Homo sapiens Coronin-2A Proteins 0.000 claims 1
- 229910000272 alkali metal oxide Inorganic materials 0.000 claims 1
- 125000003368 amide group Chemical group 0.000 claims 1
- 238000012360 testing method Methods 0.000 description 34
- KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 description 30
- 150000003254 radicals Chemical class 0.000 description 30
- 241000238631 Hexapoda Species 0.000 description 29
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 25
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 24
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 20
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 18
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 14
- 239000002904 solvent Substances 0.000 description 14
- 238000002360 preparation method Methods 0.000 description 13
- 125000000335 thiazolyl group Chemical group 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- 241000462639 Epilachna varivestis Species 0.000 description 12
- 238000000034 method Methods 0.000 description 12
- 239000006185 dispersion Substances 0.000 description 11
- 229940098779 methanesulfonic acid Drugs 0.000 description 10
- 238000003756 stirring Methods 0.000 description 10
- 239000007787 solid Substances 0.000 description 9
- 241000196324 Embryophyta Species 0.000 description 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 8
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- 125000003277 amino group Chemical group 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 7
- BRWIZMBXBAOCCF-UHFFFAOYSA-N hydrazinecarbothioamide Chemical compound NNC(N)=S BRWIZMBXBAOCCF-UHFFFAOYSA-N 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- 239000011541 reaction mixture Substances 0.000 description 7
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 7
- NDXRPDJVAUCBOH-UHFFFAOYSA-N 2,6-dimethoxybenzoyl chloride Chemical compound COC1=CC=CC(OC)=C1C(Cl)=O NDXRPDJVAUCBOH-UHFFFAOYSA-N 0.000 description 6
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 238000001816 cooling Methods 0.000 description 6
- 238000010992 reflux Methods 0.000 description 6
- 238000007363 ring formation reaction Methods 0.000 description 6
- 239000007858 starting material Substances 0.000 description 6
- 240000003259 Brassica oleracea var. botrytis Species 0.000 description 5
- 229920000742 Cotton Polymers 0.000 description 5
- 239000004480 active ingredient Substances 0.000 description 5
- 239000012496 blank sample Substances 0.000 description 5
- 235000013601 eggs Nutrition 0.000 description 5
- 230000000749 insecticidal effect Effects 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 5
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical group C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 4
- 241000254173 Coleoptera Species 0.000 description 4
- 241000255777 Lepidoptera Species 0.000 description 4
- 241000907661 Pieris rapae Species 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 150000001408 amides Chemical class 0.000 description 4
- 238000004458 analytical method Methods 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 238000009835 boiling Methods 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 230000012447 hatching Effects 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- 239000007800 oxidant agent Substances 0.000 description 4
- 241000894007 species Species 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- 125000004521 1,3,4-thiadiazol-2-yl group Chemical group S1C(=NN=C1)* 0.000 description 3
- SDYIZAANGZBOSO-UHFFFAOYSA-N 2,3-dimethoxybenzamide Chemical compound COC1=CC=CC(C(N)=O)=C1OC SDYIZAANGZBOSO-UHFFFAOYSA-N 0.000 description 3
- ZAUCRONGJXRQRD-UHFFFAOYSA-N 2,6-dimethoxybenzamide Chemical compound COC1=CC=CC(OC)=C1C(N)=O ZAUCRONGJXRQRD-UHFFFAOYSA-N 0.000 description 3
- 125000004208 3-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C([H])C(*)=C1[H] 0.000 description 3
- 125000004800 4-bromophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Br 0.000 description 3
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 description 3
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 3
- 235000011299 Brassica oleracea var botrytis Nutrition 0.000 description 3
- 235000017647 Brassica oleracea var italica Nutrition 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 244000046052 Phaseolus vulgaris Species 0.000 description 3
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical group [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 230000010933 acylation Effects 0.000 description 3
- 238000005917 acylation reaction Methods 0.000 description 3
- 239000000908 ammonium hydroxide Substances 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000011161 development Methods 0.000 description 3
- 230000018109 developmental process Effects 0.000 description 3
- 239000004495 emulsifiable concentrate Substances 0.000 description 3
- 125000005843 halogen group Chemical group 0.000 description 3
- 238000005984 hydrogenation reaction Methods 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 238000007243 oxidative cyclization reaction Methods 0.000 description 3
- 239000003208 petroleum Substances 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 3
- 239000012312 sodium hydride Substances 0.000 description 3
- 229910000104 sodium hydride Inorganic materials 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 description 2
- 125000004189 3,4-dichlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(Cl)C([H])=C1* 0.000 description 2
- 125000006305 3-iodophenyl group Chemical group [H]C1=C([H])C(I)=C([H])C(*)=C1[H] 0.000 description 2
- 125000000242 4-chlorobenzoyl group Chemical group ClC1=CC=C(C(=O)*)C=C1 0.000 description 2
- OAVULPOOAHQYDZ-UHFFFAOYSA-N 5-(4-chlorophenyl)-1,3,4-thiadiazol-2-amine Chemical compound S1C(N)=NN=C1C1=CC=C(Cl)C=C1 OAVULPOOAHQYDZ-UHFFFAOYSA-N 0.000 description 2
- 241001388466 Bruchus rufimanus Species 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- 241000255925 Diptera Species 0.000 description 2
- 241000920471 Lucilia caesar Species 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 241000257186 Phormia regina Species 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 241000382353 Pupa Species 0.000 description 2
- 241000255993 Trichoplusia ni Species 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000000443 aerosol Substances 0.000 description 2
- SOIFLUNRINLCBN-UHFFFAOYSA-N ammonium thiocyanate Chemical compound [NH4+].[S-]C#N SOIFLUNRINLCBN-UHFFFAOYSA-N 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- UKJLNMAFNRKWGR-UHFFFAOYSA-N cyclohexatrienamine Chemical group NC1=CC=C=C[CH]1 UKJLNMAFNRKWGR-UHFFFAOYSA-N 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 230000018044 dehydration Effects 0.000 description 2
- 238000006297 dehydration reaction Methods 0.000 description 2
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000004687 hexahydrates Chemical class 0.000 description 2
- 239000005457 ice water Substances 0.000 description 2
- 230000000974 larvacidal effect Effects 0.000 description 2
- 210000004185 liver Anatomy 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 239000003380 propellant Substances 0.000 description 2
- 239000000523 sample Substances 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- CUWHXIJMTMMRTI-UHFFFAOYSA-N thiadiazol-4-amine Chemical class NC1=CSN=N1 CUWHXIJMTMMRTI-UHFFFAOYSA-N 0.000 description 2
- SRVJKTDHMYAMHA-WUXMJOGZSA-N thioacetazone Chemical compound CC(=O)NC1=CC=C(\C=N\NC(N)=S)C=C1 SRVJKTDHMYAMHA-WUXMJOGZSA-N 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical class ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 1
- QUKGLNCXGVWCJX-UHFFFAOYSA-N 1,3,4-thiadiazol-2-amine Chemical class NC1=NN=CS1 QUKGLNCXGVWCJX-UHFFFAOYSA-N 0.000 description 1
- MBIZXFATKUQOOA-UHFFFAOYSA-N 1,3,4-thiadiazole Chemical compound C1=NN=CS1 MBIZXFATKUQOOA-UHFFFAOYSA-N 0.000 description 1
- LBOBESSDSGODDD-UHFFFAOYSA-N 1,3-dichloro-2-(chloromethyl)benzene Chemical compound ClCC1=C(Cl)C=CC=C1Cl LBOBESSDSGODDD-UHFFFAOYSA-N 0.000 description 1
- RAIPHJJURHTUIC-UHFFFAOYSA-N 1,3-thiazol-2-amine Chemical class NC1=NC=CS1 RAIPHJJURHTUIC-UHFFFAOYSA-N 0.000 description 1
- CPRPLWKGHKHUOQ-UHFFFAOYSA-N 2,6-dichloro-n-[5-(4-chlorophenyl)-1,3,4-thiadiazol-2-yl]benzamide Chemical compound C1=CC(Cl)=CC=C1C(S1)=NN=C1NC(=O)C1=C(Cl)C=CC=C1Cl CPRPLWKGHKHUOQ-UHFFFAOYSA-N 0.000 description 1
- CNWXNHNEEVJLNX-UHFFFAOYSA-N 2,6-dichloro-n-[5-(4-iodophenyl)-1,3,4-thiadiazol-2-yl]benzamide Chemical compound ClC1=CC=CC(Cl)=C1C(=O)NC1=NN=C(C=2C=CC(I)=CC=2)S1 CNWXNHNEEVJLNX-UHFFFAOYSA-N 0.000 description 1
- IFLZKWPGEQADRM-UHFFFAOYSA-N 2,6-dichloro-n-[5-[4-(trifluoromethyl)phenyl]-1,3,4-thiadiazol-2-yl]benzamide Chemical compound C1=CC(C(F)(F)F)=CC=C1C(S1)=NN=C1NC(=O)C1=C(Cl)C=CC=C1Cl IFLZKWPGEQADRM-UHFFFAOYSA-N 0.000 description 1
- PIEYSMVSXUFXIA-UHFFFAOYSA-N 2,6-difluoro-n-[5-(4-fluorophenyl)-1,3,4-thiadiazol-2-yl]benzamide Chemical compound C1=CC(F)=CC=C1C(S1)=NN=C1NC(=O)C1=C(F)C=CC=C1F PIEYSMVSXUFXIA-UHFFFAOYSA-N 0.000 description 1
- VCCODKSLRNPQEN-UHFFFAOYSA-N 2,6-dimethoxy-N-[5-(3,4,5-trichloropyridin-2-yl)-1,3,4-thiadiazol-2-yl]benzamide Chemical compound COC1=CC=CC(OC)=C1C(=O)NC1=NN=C(C=2C(=C(Cl)C(Cl)=CN=2)Cl)S1 VCCODKSLRNPQEN-UHFFFAOYSA-N 0.000 description 1
- AAIAPLWJDPQAMY-UHFFFAOYSA-N 2,6-dimethoxy-N-[5-[3-(trifluoromethyl)naphthalen-2-yl]-1,3,4-thiadiazol-2-yl]benzamide Chemical compound COC1=CC=CC(OC)=C1C(=O)NC1=NN=C(C=2C(=CC3=CC=CC=C3C=2)C(F)(F)F)S1 AAIAPLWJDPQAMY-UHFFFAOYSA-N 0.000 description 1
- JCLPOIIWYKRWMD-UHFFFAOYSA-N 2,6-dimethoxy-n-(5-pyridin-4-yl-1,3,4-thiadiazol-2-yl)benzamide Chemical compound COC1=CC=CC(OC)=C1C(=O)NC1=NN=C(C=2C=CN=CC=2)S1 JCLPOIIWYKRWMD-UHFFFAOYSA-N 0.000 description 1
- ARBUOWJKHXRXIT-UHFFFAOYSA-N 2,6-dimethoxy-n-(5-quinolin-3-yl-1,3,4-thiadiazol-2-yl)benzamide Chemical compound COC1=CC=CC(OC)=C1C(=O)NC1=NN=C(C=2C=C3C=CC=CC3=NC=2)S1 ARBUOWJKHXRXIT-UHFFFAOYSA-N 0.000 description 1
- FSCCDQRGDDGRKR-UHFFFAOYSA-N 2,6-dimethoxy-n-[5-(1,2-oxazol-3-yl)-1,3,4-thiadiazol-2-yl]benzamide Chemical compound COC1=CC=CC(OC)=C1C(=O)NC1=NN=C(C2=NOC=C2)S1 FSCCDQRGDDGRKR-UHFFFAOYSA-N 0.000 description 1
- HZJJHHZAKBPEJQ-UHFFFAOYSA-N 2,6-dimethoxy-n-[5-(3-phenylphenyl)-1,3,4-thiadiazol-2-yl]benzamide Chemical compound COC1=CC=CC(OC)=C1C(=O)NC1=NN=C(C=2C=C(C=CC=2)C=2C=CC=CC=2)S1 HZJJHHZAKBPEJQ-UHFFFAOYSA-N 0.000 description 1
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- NXNCWUXMOCSYKO-UHFFFAOYSA-N n-[5-(furan-2-yl)-1,3,4-thiadiazol-2-yl]-2,6-dimethoxybenzamide Chemical compound COC1=CC=CC(OC)=C1C(=O)NC1=NN=C(C=2OC=CC=2)S1 NXNCWUXMOCSYKO-UHFFFAOYSA-N 0.000 description 1
- ICFAAPMKVFCZIY-UHFFFAOYSA-N n-[5-(furan-3-yl)-1,3,4-thiadiazol-2-yl]-2,6-dimethoxybenzamide Chemical compound COC1=CC=CC(OC)=C1C(=O)NC1=NN=C(C2=COC=C2)S1 ICFAAPMKVFCZIY-UHFFFAOYSA-N 0.000 description 1
- NZHPBFGAAOMTIS-UHFFFAOYSA-N n-[5-[3,5-bis(trifluoromethyl)phenyl]-1,3,4-thiadiazol-2-yl]-2,6-dimethoxybenzamide Chemical compound COC1=CC=CC(OC)=C1C(=O)NC1=NN=C(C=2C=C(C=C(C=2)C(F)(F)F)C(F)(F)F)S1 NZHPBFGAAOMTIS-UHFFFAOYSA-N 0.000 description 1
- NPGDXKDZVLGJGP-UHFFFAOYSA-N n-[5-[3-(3-fluorophenyl)phenyl]-1,3,4-thiadiazol-2-yl]-2,6-dimethoxybenzamide Chemical compound COC1=CC=CC(OC)=C1C(=O)NC1=NN=C(C=2C=C(C=CC=2)C=2C=C(F)C=CC=2)S1 NPGDXKDZVLGJGP-UHFFFAOYSA-N 0.000 description 1
- VHUOSTWNIKRCKH-UHFFFAOYSA-N n-[5-[4-(2-chlorophenyl)phenyl]-1,3,4-thiadiazol-2-yl]-2,6-dimethoxybenzamide Chemical compound COC1=CC=CC(OC)=C1C(=O)NC1=NN=C(C=2C=CC(=CC=2)C=2C(=CC=CC=2)Cl)S1 VHUOSTWNIKRCKH-UHFFFAOYSA-N 0.000 description 1
- UWCZKJXPRHYJRS-UHFFFAOYSA-N n-[5-[4-(3-bromophenyl)phenyl]-1,3,4-thiadiazol-2-yl]-2,6-dimethoxybenzamide Chemical compound COC1=CC=CC(OC)=C1C(=O)NC1=NN=C(C=2C=CC(=CC=2)C=2C=C(Br)C=CC=2)S1 UWCZKJXPRHYJRS-UHFFFAOYSA-N 0.000 description 1
- BXTGHJIBIBKFQA-UHFFFAOYSA-N n-[[(4-chlorobenzoyl)amino]carbamothioyl]-2,6-dimethoxybenzamide Chemical compound COC1=CC=CC(OC)=C1C(=O)NC(=S)NNC(=O)C1=CC=C(Cl)C=C1 BXTGHJIBIBKFQA-UHFFFAOYSA-N 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-M naphthalene-1-sulfonate Chemical compound C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-M 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 239000000025 natural resin Substances 0.000 description 1
- 229910000510 noble metal Inorganic materials 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 125000000636 p-nitrophenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)[N+]([O-])=O 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
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 244000045947 parasite Species 0.000 description 1
- UHZYTMXLRWXGPK-UHFFFAOYSA-N phosphorus pentachloride Chemical compound ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 description 1
- DLYUQMMRRRQYAE-UHFFFAOYSA-N phosphorus pentoxide Inorganic materials O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- BGUWFUQJCDRPTL-UHFFFAOYSA-N pyridine-4-carbaldehyde Chemical compound O=CC1=CC=NC=C1 BGUWFUQJCDRPTL-UHFFFAOYSA-N 0.000 description 1
- 229910052903 pyrophyllite Inorganic materials 0.000 description 1
- JTDPJYXDDYUJBS-UHFFFAOYSA-N quinoline-2-carbohydrazide Chemical compound C1=CC=CC2=NC(C(=O)NN)=CC=C21 JTDPJYXDDYUJBS-UHFFFAOYSA-N 0.000 description 1
- ZARLOFXXUFNOHB-UHFFFAOYSA-N quinoline-3-carbohydrazide Chemical compound C1=CC=CC2=CC(C(=O)NN)=CN=C21 ZARLOFXXUFNOHB-UHFFFAOYSA-N 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 description 1
- JCWLSAUVVFLKPG-UHFFFAOYSA-N thiadiazole;hydrochloride Chemical compound Cl.C1=CSN=N1 JCWLSAUVVFLKPG-UHFFFAOYSA-N 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 235000019195 vitamin supplement Nutrition 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
- C07D285/01—Five-membered rings
- C07D285/02—Thiadiazoles; Hydrogenated thiadiazoles
- C07D285/04—Thiadiazoles; Hydrogenated thiadiazoles not condensed with other rings
- C07D285/12—1,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles
- C07D285/125—1,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical
- C07D285/135—Nitrogen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Plural Heterocyclic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US65655276A | 1976-02-09 | 1976-02-09 | |
| US74016676A | 1976-11-10 | 1976-11-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH631603A5 true CH631603A5 (en) | 1982-08-31 |
Family
ID=27097215
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH146977A CH631603A5 (en) | 1976-02-09 | 1977-02-07 | Insecticide |
Country Status (30)
| Country | Link |
|---|---|
| JP (1) | JPS52105173A (https=) |
| AR (1) | AR221204A1 (https=) |
| AT (1) | AT362192B (https=) |
| AU (1) | AU505649B2 (https=) |
| BG (3) | BG28987A4 (https=) |
| BR (1) | BR7700471A (https=) |
| CA (1) | CA1077041A (https=) |
| CH (1) | CH631603A5 (https=) |
| CS (1) | CS198217B2 (https=) |
| DD (2) | DD130038A5 (https=) |
| DE (1) | DE2704288A1 (https=) |
| DK (1) | DK50677A (https=) |
| ES (2) | ES455409A1 (https=) |
| FR (1) | FR2340312A1 (https=) |
| GB (1) | GB1571422A (https=) |
| GR (1) | GR65893B (https=) |
| HK (1) | HK27081A (https=) |
| HU (1) | HU179458B (https=) |
| IE (1) | IE44573B1 (https=) |
| IL (1) | IL51149A (https=) |
| IT (1) | IT1078058B (https=) |
| KE (1) | KE3131A (https=) |
| MY (1) | MY8200038A (https=) |
| NL (1) | NL7701059A (https=) |
| NZ (1) | NZ182937A (https=) |
| PL (2) | PL113231B1 (https=) |
| PT (1) | PT66158A (https=) |
| RO (2) | RO76588A (https=) |
| SE (1) | SE412063B (https=) |
| SU (1) | SU706023A3 (https=) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8455658B2 (en) | 2006-01-25 | 2013-06-04 | Synta Pharmaceuticals Corp. | Thiazole and thiadiazole compounds for inflammation and immune-related uses |
| EP2107054A1 (en) * | 2008-04-01 | 2009-10-07 | Università Degli Studi Di Milano - Bicocca | Antiproliferative compounds and therapeutic uses thereof |
| EP2558458B1 (de) * | 2010-04-16 | 2017-09-06 | Bayer Intellectual Property GmbH | Neue heterocyclische verbindungen als schädlingsbekämpfungsmittel |
| JP6100687B2 (ja) * | 2010-08-31 | 2017-03-22 | ダウ アグロサイエンシィズ エルエルシー | 農薬組成物 |
| JPWO2012121168A1 (ja) * | 2011-03-04 | 2014-07-17 | 国立大学法人京都大学 | キナーゼ阻害剤 |
| WO2014060381A1 (de) | 2012-10-18 | 2014-04-24 | Bayer Cropscience Ag | Heterocyclische verbindungen als schädlingsbekämpfungsmittel |
| BR112016020067B1 (pt) * | 2014-03-06 | 2021-08-31 | Bayer Cropscience Aktiengesellschaft | Compostos heterocíclicos como pesticidas. |
| WO2018108791A1 (en) * | 2016-12-16 | 2018-06-21 | Bayer Cropscience Aktiengesellschaft | Thiadiazole derivatives as pesticides |
| BR112019012584A2 (pt) * | 2016-12-22 | 2019-11-19 | Bayer Ag | heteroarilpirrolonas substituídas e sais das mesmas e uso das mesmas como substâncias ativas herbicidas |
| CN109456283B (zh) * | 2018-12-13 | 2023-03-28 | 贵州大学 | 含1,3,4-噻二唑硫醚(砜)的2-(三氟甲基)苯甲酰胺类衍生物、其制备及应用 |
-
1976
- 1976-12-18 GR GR52438A patent/GR65893B/el unknown
- 1976-12-20 IE IE2783/76A patent/IE44573B1/en unknown
- 1976-12-21 NZ NZ182937A patent/NZ182937A/xx unknown
- 1976-12-22 CA CA268,463A patent/CA1077041A/en not_active Expired
- 1976-12-23 IL IL51149A patent/IL51149A/xx unknown
-
1977
- 1977-01-11 AR AR266147A patent/AR221204A1/es active
- 1977-01-25 SE SE7700778A patent/SE412063B/xx unknown
- 1977-01-26 BR BR7700471A patent/BR7700471A/pt unknown
- 1977-01-27 ES ES455409A patent/ES455409A1/es not_active Expired
- 1977-02-01 SU SU772446348A patent/SU706023A3/ru active
- 1977-02-02 NL NL7701059A patent/NL7701059A/xx not_active Application Discontinuation
- 1977-02-02 DE DE19772704288 patent/DE2704288A1/de not_active Ceased
- 1977-02-03 GB GB4389/77A patent/GB1571422A/en not_active Expired
- 1977-02-03 BG BG037894A patent/BG28987A4/xx unknown
- 1977-02-03 BG BG035326A patent/BG28236A3/xx unknown
- 1977-02-03 BG BG037893A patent/BG28986A4/xx unknown
- 1977-02-04 PT PT66158A patent/PT66158A/pt unknown
- 1977-02-07 CH CH146977A patent/CH631603A5/de not_active IP Right Cessation
- 1977-02-07 AU AU22026/77A patent/AU505649B2/en not_active Expired
- 1977-02-07 HU HU77EI725A patent/HU179458B/hu unknown
- 1977-02-07 DK DK50677A patent/DK50677A/da not_active Application Discontinuation
- 1977-02-08 CS CS77822A patent/CS198217B2/cs unknown
- 1977-02-08 AT AT81877A patent/AT362192B/de not_active IP Right Cessation
- 1977-02-08 IT IT20057/77A patent/IT1078058B/it active
- 1977-02-09 DD DD7700197305A patent/DD130038A5/xx unknown
- 1977-02-09 JP JP1404977A patent/JPS52105173A/ja active Pending
- 1977-02-09 PL PL1977220785A patent/PL113231B1/pl unknown
- 1977-02-09 FR FR7703603A patent/FR2340312A1/fr active Granted
- 1977-02-09 DD DD77204378A patent/DD135032A5/xx unknown
- 1977-02-09 PL PL1977195892A patent/PL112645B1/pl unknown
- 1977-02-13 RO RO7796600A patent/RO76588A/ro unknown
-
1978
- 1978-02-16 ES ES467061A patent/ES467061A1/es not_active Expired
-
1979
- 1979-02-17 RO RO7996599A patent/RO76587A/ro unknown
-
1981
- 1981-06-02 KE KE3131A patent/KE3131A/xx unknown
- 1981-06-18 HK HK270/81A patent/HK27081A/xx unknown
-
1982
- 1982-12-30 MY MY38/82A patent/MY8200038A/xx unknown
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PL | Patent ceased | ||
| PL | Patent ceased |