NO752680L - - Google Patents
Info
- Publication number
- NO752680L NO752680L NO752680A NO752680A NO752680L NO 752680 L NO752680 L NO 752680L NO 752680 A NO752680 A NO 752680A NO 752680 A NO752680 A NO 752680A NO 752680 L NO752680 L NO 752680L
- Authority
- NO
- Norway
- Prior art keywords
- thiadiazol
- hydroxy
- imidazolidin
- allyl
- alkyl
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 claims description 40
- 238000002360 preparation method Methods 0.000 claims description 30
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 claims description 21
- 125000000217 alkyl group Chemical group 0.000 claims description 20
- 230000002363 herbicidal effect Effects 0.000 claims description 16
- 239000000203 mixture Substances 0.000 claims description 16
- 238000010992 reflux Methods 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 12
- SPEUIVXLLWOEMJ-UHFFFAOYSA-N acetaldehyde dimethyl acetal Natural products COC(C)OC SPEUIVXLLWOEMJ-UHFFFAOYSA-N 0.000 claims description 10
- 125000003342 alkenyl group Chemical group 0.000 claims description 8
- 125000003545 alkoxy group Chemical group 0.000 claims description 8
- 125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 claims description 7
- 125000001188 haloalkyl group Chemical group 0.000 claims description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 6
- 230000002378 acidificating effect Effects 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 239000012429 reaction media Substances 0.000 claims description 5
- -1 2-[1-methyl-3-(5-cyclopropyl-1,3,4-thiadiazol-2-yl)ureido]acetaldehyde dimethyl acetal Chemical compound 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims description 4
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 4
- 125000004414 alkyl thio group Chemical group 0.000 claims description 4
- 229910052736 halogen Inorganic materials 0.000 claims description 4
- 150000002367 halogens Chemical group 0.000 claims description 4
- 238000010438 heat treatment Methods 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- 150000001241 acetals Chemical class 0.000 claims description 3
- RQCPTHGFZZTXRL-UHFFFAOYSA-N 1-(thiadiazol-4-yl)imidazolidin-2-one Chemical class O=C1NCCN1C1=CSN=N1 RQCPTHGFZZTXRL-UHFFFAOYSA-N 0.000 claims description 2
- 239000012431 aqueous reaction media Substances 0.000 claims 1
- 241000196324 Embryophyta Species 0.000 description 33
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 27
- 239000011541 reaction mixture Substances 0.000 description 25
- 238000006243 chemical reaction Methods 0.000 description 19
- 239000000047 product Substances 0.000 description 16
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 15
- 239000004009 herbicide Substances 0.000 description 12
- 239000002244 precipitate Substances 0.000 description 11
- 239000003921 oil Substances 0.000 description 10
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 9
- 239000011521 glass Substances 0.000 description 9
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 8
- 239000000706 filtrate Substances 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 241001290610 Abildgaardia Species 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 239000000428 dust Substances 0.000 description 5
- 239000002689 soil Substances 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- VVJKKWFAADXIJK-UHFFFAOYSA-N Allylamine Chemical compound NCC=C VVJKKWFAADXIJK-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 230000006378 damage Effects 0.000 description 4
- 229910001873 dinitrogen Inorganic materials 0.000 description 4
- 239000003995 emulsifying agent Substances 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- 238000001914 filtration Methods 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- 239000012047 saturated solution Substances 0.000 description 4
- 239000002002 slurry Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- LJGUQVJJWFWIBA-UHFFFAOYSA-N 2-isocyanato-5-(trifluoromethyl)-1,3,4-thiadiazole Chemical class FC(F)(F)C1=NN=C(N=C=O)S1 LJGUQVJJWFWIBA-UHFFFAOYSA-N 0.000 description 3
- TWAUUVMXSRYMPA-UHFFFAOYSA-N 2-tert-butyl-5-isocyanato-1,3,4-thiadiazole Chemical class CC(C)(C)C1=NN=C(N=C=O)S1 TWAUUVMXSRYMPA-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
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000000539 dimer Substances 0.000 description 3
- 239000004495 emulsifiable concentrate Substances 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 239000012948 isocyanate Substances 0.000 description 3
- 150000002513 isocyanates Chemical class 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 231100000331 toxic Toxicity 0.000 description 3
- 230000002588 toxic effect Effects 0.000 description 3
- ULRLJDCNAUTJOS-UHFFFAOYSA-N 2-(prop-2-enylamino)acetaldehyde Chemical compound C=CCNCC=O ULRLJDCNAUTJOS-UHFFFAOYSA-N 0.000 description 2
- JUPUBWHBHDEZIX-UHFFFAOYSA-N 2-cyclopropyl-5-isocyanato-1,3,4-thiadiazole Chemical class S1C(N=C=O)=NN=C1C1CC1 JUPUBWHBHDEZIX-UHFFFAOYSA-N 0.000 description 2
- LTEUXHSAYOSFGQ-UHFFFAOYSA-N 5-(trifluoromethyl)-1,3,4-thiadiazol-2-amine Chemical compound NC1=NN=C(C(F)(F)F)S1 LTEUXHSAYOSFGQ-UHFFFAOYSA-N 0.000 description 2
- AVLUMBXGKFNNAS-UHFFFAOYSA-N 5-cyclopropyl-1,3,4-thiadiazol-2-amine Chemical compound S1C(N)=NN=C1C1CC1 AVLUMBXGKFNNAS-UHFFFAOYSA-N 0.000 description 2
- ICXDPEFCLDSXLI-UHFFFAOYSA-N 5-tert-butyl-1,3,4-thiadiazol-2-amine Chemical compound CC(C)(C)C1=NN=C(N)S1 ICXDPEFCLDSXLI-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 241000272814 Anser sp. Species 0.000 description 2
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- 240000008100 Brassica rapa Species 0.000 description 2
- 244000281762 Chenopodium ambrosioides Species 0.000 description 2
- 241000132536 Cirsium Species 0.000 description 2
- 240000004153 Hibiscus sabdariffa Species 0.000 description 2
- 235000001018 Hibiscus sabdariffa Nutrition 0.000 description 2
- 239000005909 Kieselgur Substances 0.000 description 2
- 241000209082 Lolium Species 0.000 description 2
- 244000236458 Panicum colonum Species 0.000 description 2
- 235000015225 Panicum colonum Nutrition 0.000 description 2
- 244000292697 Polygonum aviculare Species 0.000 description 2
- 235000006386 Polygonum aviculare Nutrition 0.000 description 2
- 235000005291 Rumex acetosa Nutrition 0.000 description 2
- 244000062793 Sorghum vulgare Species 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 239000000443 aerosol Substances 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 239000002837 defoliant Substances 0.000 description 2
- 239000002274 desiccant Substances 0.000 description 2
- DLLJVQNYBYOKGS-UHFFFAOYSA-N ethoxyethane;pentane Chemical compound CCCCC.CCOCC DLLJVQNYBYOKGS-UHFFFAOYSA-N 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 244000144972 livestock Species 0.000 description 2
- 239000012430 organic reaction media Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 208000037974 severe injury Diseases 0.000 description 2
- 230000009528 severe injury Effects 0.000 description 2
- 235000003513 sheep sorrel Nutrition 0.000 description 2
- 241000894007 species Species 0.000 description 2
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- VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 description 2
- QFUSOYKIDBRREL-NSCUHMNNSA-N (e)-but-2-en-1-amine Chemical compound C\C=C\CN QFUSOYKIDBRREL-NSCUHMNNSA-N 0.000 description 1
- VWJYDONMXDIHNY-NSCUHMNNSA-N (e)-pent-3-en-1-amine Chemical compound C\C=C\CCN VWJYDONMXDIHNY-NSCUHMNNSA-N 0.000 description 1
- MBIZXFATKUQOOA-UHFFFAOYSA-N 1,3,4-thiadiazole Chemical compound C1=NN=CS1 MBIZXFATKUQOOA-UHFFFAOYSA-N 0.000 description 1
- QXTRPGAMVIONMK-UHFFFAOYSA-N 2-amino-5-ethyl-1,3,4-thiadiazole Chemical compound CCC1=NN=C(N)S1 QXTRPGAMVIONMK-UHFFFAOYSA-N 0.000 description 1
- LILXDMFJXYAKMK-UHFFFAOYSA-N 2-bromo-1,1-diethoxyethane Chemical compound CCOC(CBr)OCC LILXDMFJXYAKMK-UHFFFAOYSA-N 0.000 description 1
- VUGCBIWQHSRQBZ-UHFFFAOYSA-N 2-methylbut-3-yn-2-amine Chemical compound CC(C)(N)C#C VUGCBIWQHSRQBZ-UHFFFAOYSA-N 0.000 description 1
- KZXPZRPMVOQFGU-UHFFFAOYSA-N 3-(5-cyclopropyl-1,3,4-thiadiazol-2-yl)-1-methyl-1-(2-oxoethyl)urea Chemical compound S1C(NC(=O)N(CC=O)C)=NN=C1C1CC1 KZXPZRPMVOQFGU-UHFFFAOYSA-N 0.000 description 1
- ASVKKRLMJCWVQF-UHFFFAOYSA-N 3-buten-1-amine Chemical compound NCCC=C ASVKKRLMJCWVQF-UHFFFAOYSA-N 0.000 description 1
- WHNOKDNCUNZBLW-UHFFFAOYSA-N 3-ethylpent-1-yn-3-amine Chemical compound CCC(N)(CC)C#C WHNOKDNCUNZBLW-UHFFFAOYSA-N 0.000 description 1
- MEWGEKDPUUYFFK-UHFFFAOYSA-N 4-(5-amino-1,3,4-thiadiazol-2-yl)cyclohexan-1-ol Chemical compound S1C(N)=NN=C1C1CCC(O)CC1 MEWGEKDPUUYFFK-UHFFFAOYSA-N 0.000 description 1
- DYUZZXXUVYQTQX-UHFFFAOYSA-N 4-chlorobut-2-en-1-amine Chemical compound NCC=CCCl DYUZZXXUVYQTQX-UHFFFAOYSA-N 0.000 description 1
- OOTFUIFRKQZJBL-UHFFFAOYSA-N 4-ethynylheptan-4-amine Chemical compound CCCC(N)(C#C)CCC OOTFUIFRKQZJBL-UHFFFAOYSA-N 0.000 description 1
- JNLJSNYXTFJREJ-UHFFFAOYSA-N 5-(2-methylcyclobutyl)-1,3,4-thiadiazol-2-amine Chemical compound CC1CCC1C1=NN=C(N)S1 JNLJSNYXTFJREJ-UHFFFAOYSA-N 0.000 description 1
- IUHFEYROBNRTEL-UHFFFAOYSA-N 5-(3-chloropropyl)-1,3,4-thiadiazol-2-amine Chemical compound NC1=NN=C(CCCCl)S1 IUHFEYROBNRTEL-UHFFFAOYSA-N 0.000 description 1
- RVOGJFQLYAYIPT-UHFFFAOYSA-N 5-(3-ethylcycloheptyl)-1,3,4-thiadiazol-2-amine Chemical compound C1C(CC)CCCCC1C1=NN=C(N)S1 RVOGJFQLYAYIPT-UHFFFAOYSA-N 0.000 description 1
- LQALYNSTKSKAAB-UHFFFAOYSA-N 5-(3-methoxycyclopentyl)-1,3,4-thiadiazol-2-amine Chemical compound C1C(OC)CCC1C1=NN=C(N)S1 LQALYNSTKSKAAB-UHFFFAOYSA-N 0.000 description 1
- NZIABVKHVKUYPN-UHFFFAOYSA-N 5-(3-propoxycyclohexyl)-1,3,4-thiadiazol-2-amine Chemical compound C1C(OCCC)CCCC1C1=NN=C(N)S1 NZIABVKHVKUYPN-UHFFFAOYSA-N 0.000 description 1
- BJHQURKFQGJTES-UHFFFAOYSA-N 5-(4-bromocyclohexyl)-1,3,4-thiadiazol-2-amine Chemical compound S1C(N)=NN=C1C1CCC(Br)CC1 BJHQURKFQGJTES-UHFFFAOYSA-N 0.000 description 1
- MWELBRHHUMTOSI-UHFFFAOYSA-N 5-(4-chlorocyclohexyl)-1,3,4-thiadiazol-2-amine Chemical compound S1C(N)=NN=C1C1CCC(Cl)CC1 MWELBRHHUMTOSI-UHFFFAOYSA-N 0.000 description 1
- PDUVPBCMEMJQGB-UHFFFAOYSA-N 5-(chloromethyl)-1,3,4-thiadiazol-2-amine Chemical compound NC1=NN=C(CCl)S1 PDUVPBCMEMJQGB-UHFFFAOYSA-N 0.000 description 1
- KMICNGJJXVPIQO-UHFFFAOYSA-N 5-(trichloromethyl)-1,3,4-thiadiazol-2-amine Chemical compound NC1=NN=C(C(Cl)(Cl)Cl)S1 KMICNGJJXVPIQO-UHFFFAOYSA-N 0.000 description 1
- UDPUNVVGMBRZKE-UHFFFAOYSA-N 5-butoxy-1,3,4-thiadiazol-2-amine Chemical compound CCCCOC1=NN=C(N)S1 UDPUNVVGMBRZKE-UHFFFAOYSA-N 0.000 description 1
- XAXBPOUZBWKKJS-UHFFFAOYSA-N 5-butylsulfinyl-1,3,4-thiadiazol-2-amine Chemical compound CCCCS(=O)C1=NN=C(N)S1 XAXBPOUZBWKKJS-UHFFFAOYSA-N 0.000 description 1
- QPLFNKQUAMIOGI-UHFFFAOYSA-N 5-butylsulfonyl-1,3,4-thiadiazol-2-amine Chemical compound CCCCS(=O)(=O)C1=NN=C(N)S1 QPLFNKQUAMIOGI-UHFFFAOYSA-N 0.000 description 1
- ROBHTWLKDVLHNY-UHFFFAOYSA-N 5-cyclobutyl-1,3,4-thiadiazol-2-amine Chemical compound S1C(N)=NN=C1C1CCC1 ROBHTWLKDVLHNY-UHFFFAOYSA-N 0.000 description 1
- IKOPPSIEFDHKOR-UHFFFAOYSA-N 5-cycloheptyl-1,3,4-thiadiazol-2-amine Chemical compound S1C(N)=NN=C1C1CCCCCC1 IKOPPSIEFDHKOR-UHFFFAOYSA-N 0.000 description 1
- BLBDGPFJLDEFFL-UHFFFAOYSA-N 5-cyclohexyl-1,3,4-thiadiazol-2-amine Chemical compound S1C(N)=NN=C1C1CCCCC1 BLBDGPFJLDEFFL-UHFFFAOYSA-N 0.000 description 1
- MGSBORAJOCQFOK-UHFFFAOYSA-N 5-cyclopentyl-1,3,4-thiadiazol-2-amine Chemical compound S1C(N)=NN=C1C1CCCC1 MGSBORAJOCQFOK-UHFFFAOYSA-N 0.000 description 1
- UNWILELBTFFRJV-UHFFFAOYSA-N 5-ethoxy-1,3,4-thiadiazol-2-amine Chemical compound CCOC1=NN=C(N)S1 UNWILELBTFFRJV-UHFFFAOYSA-N 0.000 description 1
- VWRHSNKTSSIMGE-UHFFFAOYSA-N 5-ethylsulfanyl-1,3,4-thiadiazol-2-amine Chemical compound CCSC1=NN=C(N)S1 VWRHSNKTSSIMGE-UHFFFAOYSA-N 0.000 description 1
- NIMCWMVFUNIBEL-UHFFFAOYSA-N 5-ethylsulfinyl-1,3,4-thiadiazol-2-amine Chemical compound CCS(=O)C1=NN=C(N)S1 NIMCWMVFUNIBEL-UHFFFAOYSA-N 0.000 description 1
- NGDMEHKMIPBRDA-UHFFFAOYSA-N 5-ethylsulfonyl-1,3,4-thiadiazol-2-amine Chemical compound CCS(=O)(=O)C1=NN=C(N)S1 NGDMEHKMIPBRDA-UHFFFAOYSA-N 0.000 description 1
- UDPZHCABSWZTLM-UHFFFAOYSA-N 5-hexoxy-1,3,4-thiadiazol-2-amine Chemical compound CCCCCCOC1=NN=C(N)S1 UDPZHCABSWZTLM-UHFFFAOYSA-N 0.000 description 1
- ZDNFTCAEGDVXJB-UHFFFAOYSA-N 5-hexylsulfonyl-1,3,4-thiadiazol-2-amine Chemical compound CCCCCCS(=O)(=O)C1=NN=C(N)S1 ZDNFTCAEGDVXJB-UHFFFAOYSA-N 0.000 description 1
- DRHLSQJZTGPDMP-UHFFFAOYSA-N 5-methoxy-1,3,4-thiadiazol-2-amine Chemical compound COC1=NN=C(N)S1 DRHLSQJZTGPDMP-UHFFFAOYSA-N 0.000 description 1
- HMPUHXCGUHDVBI-UHFFFAOYSA-N 5-methyl-1,3,4-thiadiazol-2-amine Chemical compound CC1=NN=C(N)S1 HMPUHXCGUHDVBI-UHFFFAOYSA-N 0.000 description 1
- PCLAZAJARAIGGD-UHFFFAOYSA-N 5-methylsulfanyl-1,3,4-thiadiazol-2-amine Chemical compound CSC1=NN=C(N)S1 PCLAZAJARAIGGD-UHFFFAOYSA-N 0.000 description 1
- GXPKJOYKJDOUKX-UHFFFAOYSA-N 5-methylsulfonyl-1,3,4-thiadiazol-2-amine Chemical compound CS(=O)(=O)C1=NN=C(N)S1 GXPKJOYKJDOUKX-UHFFFAOYSA-N 0.000 description 1
- DSSWCGPUVTWPPT-UHFFFAOYSA-N 5-pent-3-enyl-1,3,4-thiadiazol-2-amine Chemical compound CC=CCCC1=NN=C(N)S1 DSSWCGPUVTWPPT-UHFFFAOYSA-N 0.000 description 1
- ZQWRZVFWBDLVBP-UHFFFAOYSA-N 5-propoxy-1,3,4-thiadiazol-2-amine Chemical compound CCCOC1=NN=C(N)S1 ZQWRZVFWBDLVBP-UHFFFAOYSA-N 0.000 description 1
- NLQURINLKRAGIF-UHFFFAOYSA-N 5-propyl-1,3,4-thiadiazol-2-amine Chemical compound CCCC1=NN=C(N)S1 NLQURINLKRAGIF-UHFFFAOYSA-N 0.000 description 1
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- 235000014720 Myrica gale Nutrition 0.000 description 1
- 244000024215 Myrica gale Species 0.000 description 1
- 241000721619 Najas Species 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 240000001439 Opuntia Species 0.000 description 1
- 235000013389 Opuntia humifusa var. humifusa Nutrition 0.000 description 1
- 241001148659 Panicum dichotomiflorum Species 0.000 description 1
- 241001520808 Panicum virgatum Species 0.000 description 1
- 240000000275 Persicaria hydropiper Species 0.000 description 1
- 235000017337 Persicaria hydropiper Nutrition 0.000 description 1
- 235000004442 Polygonum persicaria Nutrition 0.000 description 1
- 241001494501 Prosopis <angiosperm> Species 0.000 description 1
- 235000001560 Prosopis chilensis Nutrition 0.000 description 1
- 235000014460 Prosopis juliflora var juliflora Nutrition 0.000 description 1
- 235000002357 Ribes grossularia Nutrition 0.000 description 1
- 244000171263 Ribes grossularia Species 0.000 description 1
- 244000275012 Sesbania cannabina Species 0.000 description 1
- 235000002834 Sida rhombifolia Nutrition 0.000 description 1
- 240000003194 Sida rhombifolia Species 0.000 description 1
- 240000002439 Sorghum halepense Species 0.000 description 1
- 235000011684 Sorghum saccharatum Nutrition 0.000 description 1
- 240000001949 Taraxacum officinale Species 0.000 description 1
- 235000005187 Taraxacum officinale ssp. officinale Nutrition 0.000 description 1
- 241000201404 Verbascum blattaria Species 0.000 description 1
- 235000010599 Verbascum thapsus Nutrition 0.000 description 1
- 244000178289 Verbascum thapsus Species 0.000 description 1
- 244000145469 Vernonia anthelmintica Species 0.000 description 1
- 235000013018 Vernonia anthelmintica Nutrition 0.000 description 1
- 241000219873 Vicia Species 0.000 description 1
- 208000000260 Warts Diseases 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 235000003484 annual ragweed Nutrition 0.000 description 1
- 239000001138 artemisia absinthium Substances 0.000 description 1
- 229960000892 attapulgite Drugs 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 235000005770 birds nest Nutrition 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 244000082778 bunchy flat sedge Species 0.000 description 1
- 235000006263 bur ragweed Nutrition 0.000 description 1
- ZZRMYOZQUCUWFT-UHFFFAOYSA-N but-3-yn-2-amine Chemical compound CC(N)C#C ZZRMYOZQUCUWFT-UHFFFAOYSA-N 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 235000013351 cheese Nutrition 0.000 description 1
- 125000004965 chloroalkyl group Chemical group 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 235000003488 common ragweed Nutrition 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 235000021438 curry Nutrition 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- OAYLNYINCPYISS-UHFFFAOYSA-N ethyl acetate;hexane Chemical compound CCCCCC.CCOC(C)=O OAYLNYINCPYISS-UHFFFAOYSA-N 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- FICBXRYQMBKLJJ-UHFFFAOYSA-N hex-5-en-1-amine Chemical compound NCCCCC=C FICBXRYQMBKLJJ-UHFFFAOYSA-N 0.000 description 1
- 230000000415 inactivating effect Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 235000019713 millet Nutrition 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 230000009526 moderate injury Effects 0.000 description 1
- 239000005645 nematicide Substances 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- UVBBCQLPTZEDHT-UHFFFAOYSA-N pent-4-en-1-amine Chemical compound NCCCC=C UVBBCQLPTZEDHT-UHFFFAOYSA-N 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- JKANAVGODYYCQF-UHFFFAOYSA-N prop-2-yn-1-amine Chemical compound NCC#C JKANAVGODYYCQF-UHFFFAOYSA-N 0.000 description 1
- 229910052903 pyrophyllite Inorganic materials 0.000 description 1
- 235000009736 ragweed Nutrition 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 201000010153 skin papilloma Diseases 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 150000004867 thiadiazoles Chemical class 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 244000045561 useful plants Species 0.000 description 1
- 239000010455 vermiculite Substances 0.000 description 1
- 229910052902 vermiculite Inorganic materials 0.000 description 1
- 235000019354 vermiculite Nutrition 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 235000005765 wild carrot Nutrition 0.000 description 1
- 239000008096 xylene Substances 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Plural Heterocyclic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/494,441 US4028375A (en) | 1974-08-05 | 1974-08-05 | Thiadiazolylimidazolidinones |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO752680L true NO752680L (hu) | 1976-02-06 |
Family
ID=23964486
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO752680A NO752680L (hu) | 1974-08-05 | 1975-07-30 |
Country Status (26)
| Country | Link |
|---|---|
| US (2) | US4028375A (hu) |
| JP (1) | JPS5141435A (hu) |
| KR (1) | KR800000505B1 (hu) |
| AR (1) | AR220882A1 (hu) |
| AT (1) | AT345815B (hu) |
| AU (1) | AU497283B2 (hu) |
| BE (1) | BE832126A (hu) |
| BR (1) | BR7504964A (hu) |
| CA (1) | CA1046516A (hu) |
| CH (1) | CH613702A5 (hu) |
| DE (1) | DE2534993A1 (hu) |
| DK (1) | DK353575A (hu) |
| EG (1) | EG11730A (hu) |
| ES (1) | ES439889A1 (hu) |
| FR (1) | FR2281364A1 (hu) |
| GB (1) | GB1500027A (hu) |
| IL (1) | IL47867A (hu) |
| IN (1) | IN142194B (hu) |
| IT (1) | IT1041134B (hu) |
| NL (1) | NL7509257A (hu) |
| NO (1) | NO752680L (hu) |
| NZ (1) | NZ178231A (hu) |
| SE (1) | SE426821B (hu) |
| SU (1) | SU826937A3 (hu) |
| YU (1) | YU39471B (hu) |
| ZA (1) | ZA754841B (hu) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4195181A (en) * | 1973-01-23 | 1980-03-25 | Bayer Aktiengesellschaft | 1,3,4-Thiadiazole compounds and herbicidal compositions |
| US4086238A (en) * | 1976-06-21 | 1978-04-25 | Velsicol Chemical Corporation | 1-Thiadiazolyl-4-methoxymethyl-5-hydroxyimidazolidinones |
| US4233057A (en) * | 1979-05-14 | 1980-11-11 | Ppg Industries, Inc. | 3-[5-(1-Phenoxy-alkyl, -alkynyl, -alkenyl, or haloalkyl)-1,3,4-thiadiazol-2-yl]-4-hydroxy-1-methyl-2-imidazolidinones |
| US4264353A (en) * | 1979-06-04 | 1981-04-28 | Ppg Industries, Inc. | 3-[5-[1-(4-Halophenoxy)alkyl, alkynyl, alkenyl, or haloalkyl]-1,3,4-thiadiazol-2-yl]-4-hydroxy-1-methyl-2-imidazolidinones |
| US4269983A (en) * | 1979-06-18 | 1981-05-26 | Ppg Industries, Inc. | 3-[5-[1-(2 or 3-Halophenoxy)alkyl, alkynyl, alkenyl, or haloalkyl]-1,3,4-thiadiazol-2-yl]-4-hydroxy-1-methyl-2-imidazolidinones |
| US4252960A (en) * | 1979-06-18 | 1981-02-24 | Ppg Industries, Inc. | Intermediates of and methods of making 3-[5-[1-(nitrophenoxy)alkyl, alkynyl, alkenyl or haloalkyl]-1,3,4-thiadiazol-2-yl]-4-hydroxy-1-methyl-2-imidazolidinones |
| US4252961A (en) * | 1979-06-18 | 1981-02-24 | Ppg Industries, Inc. | Intermediates of and process for making 3-[5-[1-(2-, 3-, or 4-methyl, or ethyl or isopropylphenoxy)alkyl, alkynyl, alkenyl, or haloalkyl]-1,3,4-thiadiazol-2-yl]-4-hydroxy-1-methyl-2-imidazolidinones |
| US4230480A (en) * | 1979-06-18 | 1980-10-28 | Ppg Industries, Inc. | 3-[5-(1-(Nitrophenoxy)alkyl, alkynyl, alkenyl, or haloalkyl)-1,3,4-thiadiazol-2-yl]-4-hydroxy-1-methyl-2-imidazolidinones |
| US4218236A (en) * | 1979-06-18 | 1980-08-19 | Ppg Industries, Inc. | 3-[5-[1-(2-, 3-, or 4-methyl, or ethyl or isopropylphenoxy) alkyl, alkynyl, haloalkyl]-1,3,4-thiadiazol-2-yl]-4-hydroxy-1-methyl methyl-2-imidazolidinones |
| US4268675A (en) * | 1979-07-06 | 1981-05-19 | Ppg Industries, Inc. | 3-[5-[1-(Dihalophenoxy)alkyl, alkynyl, alkenyl, or haloalkyl]-1,3,4-thiadiazol-2-yl]-4-hydroxy-1-methyl-2-imidazolidinones |
| US4314842A (en) * | 1979-08-10 | 1982-02-09 | Ppg Industries, Inc. | Herbicidal substituted 1,3,4-thiadiazol-2-yl-4-hydroxy-1-methyl-2-imidazolidinones |
| US4426527A (en) | 1982-02-12 | 1984-01-17 | Ppg Industries, Inc. | 3-[5- Or 3-substituted-1,2,4-oxadiazol-3- or -5-yl]-1-substituted-4-substituted-5-substituted or unsubstituted-2-imidazolidinones |
| US4857099A (en) * | 1982-02-12 | 1989-08-15 | American Cyanamid Company | Terrestrial and aquatic herbicidal methods |
| US4918086A (en) * | 1987-08-07 | 1990-04-17 | Ciba-Geigy Corporation | 1-nitro-2,2-diaminoethylene derivatives |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2013407A1 (de) * | 1970-03-20 | 1971-10-07 | 1 (1,3,4 Thiadiazol 2 yl) lmidazohdi non (2) Derivate, Verfahren zu ihrer Her stellung und ihre Verwendung als herbizide | |
| DE2013406A1 (de) * | 1970-03-20 | 1971-10-07 | 1(13 4 Thiadiazol 2 yl) lmidazohdi non (2) Derivate, Verfahren zu ihrer Her stellung und ihre Verwendung als herbizide | |
| US3773780A (en) * | 1971-03-10 | 1973-11-20 | Bayer Ag | 1-(1,3,4-thiadiazol-2-yl)-imidazolidinone-(2)compounds |
| ZA741626B (en) * | 1973-06-29 | 1975-02-26 | Velsicol Chemical Corp | New thiadiazolylimidazolidinones |
| CA1042898A (en) * | 1974-01-10 | 1978-11-21 | Velsicol Chemical Corporation | Thiadiazolylimidazolidinones |
-
1974
- 1974-08-05 US US05/494,441 patent/US4028375A/en not_active Expired - Lifetime
-
1975
- 1975-06-23 AR AR259305A patent/AR220882A1/es active
- 1975-07-22 CA CA231,968A patent/CA1046516A/en not_active Expired
- 1975-07-28 ZA ZA00754841A patent/ZA754841B/xx unknown
- 1975-07-28 NZ NZ178231A patent/NZ178231A/xx unknown
- 1975-07-30 NO NO752680A patent/NO752680L/no unknown
- 1975-07-30 IN IN1502/CAL/75A patent/IN142194B/en unknown
- 1975-07-31 ES ES439889A patent/ES439889A1/es not_active Expired
- 1975-08-01 GB GB32171/75A patent/GB1500027A/en not_active Expired
- 1975-08-04 IL IL47867A patent/IL47867A/xx unknown
- 1975-08-04 IT IT50813/75A patent/IT1041134B/it active
- 1975-08-04 BR BR7504964*A patent/BR7504964A/pt unknown
- 1975-08-04 KR KR7501707A patent/KR800000505B1/ko active
- 1975-08-04 CH CH1014175A patent/CH613702A5/xx not_active IP Right Cessation
- 1975-08-04 NL NL7509257A patent/NL7509257A/xx not_active Application Discontinuation
- 1975-08-04 SE SE7508783A patent/SE426821B/xx unknown
- 1975-08-04 AU AU83655/75A patent/AU497283B2/en not_active Expired
- 1975-08-04 DK DK353575A patent/DK353575A/da unknown
- 1975-08-04 AT AT602775A patent/AT345815B/de not_active IP Right Cessation
- 1975-08-05 EG EG474/75A patent/EG11730A/xx active
- 1975-08-05 YU YU2011/75A patent/YU39471B/xx unknown
- 1975-08-05 DE DE19752534993 patent/DE2534993A1/de not_active Ceased
- 1975-08-05 SU SU752163138A patent/SU826937A3/ru active
- 1975-08-05 JP JP50095318A patent/JPS5141435A/ja active Pending
- 1975-08-05 FR FR7524416A patent/FR2281364A1/fr active Granted
- 1975-08-05 BE BE158943A patent/BE832126A/xx not_active IP Right Cessation
-
1977
- 1977-04-07 US US05/785,711 patent/US4093443A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| EG11730A (en) | 1978-03-29 |
| DE2534993A1 (de) | 1976-02-26 |
| KR800000505B1 (ko) | 1980-06-12 |
| BR7504964A (pt) | 1976-07-27 |
| SE7508783L (sv) | 1976-02-06 |
| IL47867A0 (en) | 1975-11-25 |
| ATA602775A (de) | 1978-02-15 |
| AU8365575A (en) | 1977-02-10 |
| US4093443A (en) | 1978-06-06 |
| IN142194B (hu) | 1977-06-11 |
| YU201175A (en) | 1982-02-28 |
| NZ178231A (en) | 1978-04-03 |
| GB1500027A (en) | 1978-02-08 |
| YU39471B (en) | 1984-12-31 |
| AU497283B2 (en) | 1978-12-07 |
| AR220882A1 (es) | 1980-12-15 |
| ZA754841B (en) | 1976-06-30 |
| DK353575A (da) | 1976-02-06 |
| SU826937A3 (ru) | 1981-04-30 |
| IT1041134B (it) | 1980-01-10 |
| AT345815B (de) | 1978-10-10 |
| CH613702A5 (hu) | 1979-10-15 |
| IL47867A (en) | 1978-09-29 |
| FR2281364B1 (hu) | 1978-09-22 |
| ES439889A1 (es) | 1977-02-16 |
| BE832126A (fr) | 1975-12-01 |
| FR2281364A1 (fr) | 1976-03-05 |
| CA1046516A (en) | 1979-01-16 |
| JPS5141435A (hu) | 1976-04-07 |
| NL7509257A (nl) | 1976-02-09 |
| US4028375A (en) | 1977-06-07 |
| SE426821B (sv) | 1983-02-14 |
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