CN1283191A - 亚苄基吡唑啉酮、其制备和应用 - Google Patents
亚苄基吡唑啉酮、其制备和应用 Download PDFInfo
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- CN1283191A CN1283191A CN98812494A CN98812494A CN1283191A CN 1283191 A CN1283191 A CN 1283191A CN 98812494 A CN98812494 A CN 98812494A CN 98812494 A CN98812494 A CN 98812494A CN 1283191 A CN1283191 A CN 1283191A
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- Prior art keywords
- base
- alkyl
- cis
- dihydro
- replace
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- -1 Benzylidene pyrazolones Chemical class 0.000 title claims abstract description 293
- 229940051880 analgesics and antipyretics pyrazolones Drugs 0.000 title claims abstract description 24
- 238000002360 preparation method Methods 0.000 title claims description 11
- 239000000460 chlorine Chemical group 0.000 claims abstract description 946
- 150000001875 compounds Chemical class 0.000 claims abstract description 47
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 46
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 41
- 150000002367 halogens Chemical class 0.000 claims abstract description 40
- 239000000203 mixture Substances 0.000 claims abstract description 36
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 28
- 239000001257 hydrogen Substances 0.000 claims abstract description 28
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 24
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims abstract description 20
- 229910052794 bromium Chemical group 0.000 claims abstract description 20
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 19
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract description 15
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 15
- 229920006395 saturated elastomer Polymers 0.000 claims abstract description 14
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims abstract description 12
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract description 12
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 9
- 125000004433 nitrogen atom Chemical group N* 0.000 claims abstract description 6
- 239000001301 oxygen Substances 0.000 claims abstract description 5
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 5
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 4
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims abstract description 4
- 150000003457 sulfones Chemical class 0.000 claims abstract description 4
- 150000003462 sulfoxides Chemical class 0.000 claims abstract description 4
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims abstract 11
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 34
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 25
- 241000196324 Embryophyta Species 0.000 claims description 23
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 20
- 125000003545 alkoxy group Chemical group 0.000 claims description 13
- 125000000217 alkyl group Chemical group 0.000 claims description 12
- 230000000694 effects Effects 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 12
- 238000006243 chemical reaction Methods 0.000 claims description 9
- UYMQWGLCXYHTES-UHFFFAOYSA-N phenyl(1h-pyrazol-5-yl)methanone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=NN1 UYMQWGLCXYHTES-UHFFFAOYSA-N 0.000 claims description 9
- 125000003373 pyrazinyl group Chemical group 0.000 claims description 9
- 238000009333 weeding Methods 0.000 claims description 9
- WQADWIOXOXRPLN-UHFFFAOYSA-N 1,3-dithiane Chemical compound C1CSCSC1 WQADWIOXOXRPLN-UHFFFAOYSA-N 0.000 claims description 8
- NHZLLKNRTDIFAD-UHFFFAOYSA-N 2,5-dihydro-1,3-oxazole Chemical compound C1OCN=C1 NHZLLKNRTDIFAD-UHFFFAOYSA-N 0.000 claims description 8
- ARGCQEVBJHPOGB-UHFFFAOYSA-N 2,5-dihydrofuran Chemical compound C1OCC=C1 ARGCQEVBJHPOGB-UHFFFAOYSA-N 0.000 claims description 8
- BBVIDBNAYOIXOE-UHFFFAOYSA-N 1,2,4-oxadiazole Chemical compound C=1N=CON=1 BBVIDBNAYOIXOE-UHFFFAOYSA-N 0.000 claims description 6
- FKASFBLJDCHBNZ-UHFFFAOYSA-N 1,3,4-oxadiazole Chemical compound C1=NN=CO1 FKASFBLJDCHBNZ-UHFFFAOYSA-N 0.000 claims description 5
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 5
- 125000002757 morpholinyl group Chemical group 0.000 claims description 5
- JQIZHNLEFQMDCQ-UHFFFAOYSA-N 1,2,3,4-tetrahydropyridazine Chemical compound C1CC=CNN1 JQIZHNLEFQMDCQ-UHFFFAOYSA-N 0.000 claims description 4
- OTPDWCMLUKMQNO-UHFFFAOYSA-N 1,2,3,4-tetrahydropyrimidine Chemical compound C1NCC=CN1 OTPDWCMLUKMQNO-UHFFFAOYSA-N 0.000 claims description 4
- HTJMXYRLEDBSLT-UHFFFAOYSA-N 1,2,4,5-tetrazine Chemical compound C1=NN=CN=N1 HTJMXYRLEDBSLT-UHFFFAOYSA-N 0.000 claims description 4
- OXBLVCZKDOZZOJ-UHFFFAOYSA-N 2,3-Dihydrothiophene Chemical compound C1CC=CS1 OXBLVCZKDOZZOJ-UHFFFAOYSA-N 0.000 claims description 4
- FJRPOHLDJUJARI-UHFFFAOYSA-N 2,3-dihydro-1,2-oxazole Chemical compound C1NOC=C1 FJRPOHLDJUJARI-UHFFFAOYSA-N 0.000 claims description 4
- ZABMHLDQFJHDSC-UHFFFAOYSA-N 2,3-dihydro-1,3-oxazole Chemical compound C1NC=CO1 ZABMHLDQFJHDSC-UHFFFAOYSA-N 0.000 claims description 4
- JKTCBAGSMQIFNL-UHFFFAOYSA-N 2,3-dihydrofuran Chemical compound C1CC=CO1 JKTCBAGSMQIFNL-UHFFFAOYSA-N 0.000 claims description 4
- OFJBYLCQNJHFMI-UHFFFAOYSA-N 2,5-dihydro-1,2-oxazole Chemical compound C1ONC=C1 OFJBYLCQNJHFMI-UHFFFAOYSA-N 0.000 claims description 4
- WURYWHAKEJHAOV-UHFFFAOYSA-N 2,5-dihydrothiophene Chemical compound C1SCC=C1 WURYWHAKEJHAOV-UHFFFAOYSA-N 0.000 claims description 4
- IMSODMZESSGVBE-UHFFFAOYSA-N 2-Oxazoline Chemical compound C1CN=CO1 IMSODMZESSGVBE-UHFFFAOYSA-N 0.000 claims description 4
- WEQPBCSPRXFQQS-UHFFFAOYSA-N 4,5-dihydro-1,2-oxazole Chemical compound C1CC=NO1 WEQPBCSPRXFQQS-UHFFFAOYSA-N 0.000 claims description 4
- YPWFISCTZQNZAU-UHFFFAOYSA-N Thiane Chemical compound C1CCSCC1 YPWFISCTZQNZAU-UHFFFAOYSA-N 0.000 claims description 4
- 125000002541 furyl group Chemical group 0.000 claims description 4
- 125000002883 imidazolyl group Chemical group 0.000 claims description 4
- 125000001786 isothiazolyl group Chemical group 0.000 claims description 4
- 125000000842 isoxazolyl group Chemical group 0.000 claims description 4
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 claims description 4
- 230000001473 noxious effect Effects 0.000 claims description 4
- 125000000160 oxazolidinyl group Chemical group 0.000 claims description 4
- 125000005936 piperidyl group Chemical group 0.000 claims description 4
- 125000002098 pyridazinyl group Chemical group 0.000 claims description 4
- 125000004076 pyridyl group Chemical group 0.000 claims description 4
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 4
- 125000005958 tetrahydrothienyl group Chemical group 0.000 claims description 4
- 125000000335 thiazolyl group Chemical group 0.000 claims description 4
- 125000001544 thienyl group Chemical group 0.000 claims description 4
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 claims description 3
- 239000011814 protection agent Substances 0.000 claims description 3
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 2
- 241000405414 Rehmannia Species 0.000 claims 1
- SMWDFEZZVXVKRB-UHFFFAOYSA-N anhydrous quinoline Natural products N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 claims 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract description 3
- 125000001424 substituent group Chemical group 0.000 abstract description 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 6
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 2
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 1
- 239000002585 base Substances 0.000 description 553
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 description 20
- 125000000437 thiazol-2-yl group Chemical group [H]C1=C([H])N=C(*)S1 0.000 description 19
- 239000011737 fluorine Substances 0.000 description 17
- 229910052731 fluorine Inorganic materials 0.000 description 17
- 239000013543 active substance Substances 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- 239000006185 dispersion Substances 0.000 description 10
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 150000002431 hydrogen Chemical class 0.000 description 9
- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 description 8
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 description 8
- 125000001541 3-thienyl group Chemical group S1C([H])=C([*])C([H])=C1[H] 0.000 description 8
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 description 8
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 8
- 239000002253 acid Substances 0.000 description 8
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 8
- 239000003921 oil Substances 0.000 description 8
- 125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 description 7
- 125000003682 3-furyl group Chemical group O1C([H])=C([*])C([H])=C1[H] 0.000 description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 7
- 238000005160 1H NMR spectroscopy Methods 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical class C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 230000002363 herbicidal effect Effects 0.000 description 6
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 6
- 125000004353 pyrazol-1-yl group Chemical group [H]C1=NN(*)C([H])=C1[H] 0.000 description 6
- 125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 description 5
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 5
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 5
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 5
- 241000209149 Zea Species 0.000 description 5
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 5
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 5
- 239000004359 castor oil Substances 0.000 description 5
- 229960001777 castor oil Drugs 0.000 description 5
- 235000019438 castor oil Nutrition 0.000 description 5
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 5
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 5
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 5
- 239000011630 iodine Substances 0.000 description 5
- 229910052740 iodine Inorganic materials 0.000 description 5
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 5
- 125000004674 methylcarbonyl group Chemical group CC(=O)* 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 241000335053 Beta vulgaris Species 0.000 description 4
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 4
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 4
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 4
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 description 4
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- 239000003337 fertilizer Substances 0.000 description 4
- 125000005816 fluoropropyl group Chemical group [H]C([H])(F)C([H])([H])C([H])([H])* 0.000 description 4
- 230000012010 growth Effects 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 4
- CFHIDWOYWUOIHU-UHFFFAOYSA-N oxomethyl Chemical compound O=[CH] CFHIDWOYWUOIHU-UHFFFAOYSA-N 0.000 description 4
- 238000000746 purification Methods 0.000 description 4
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- 150000003839 salts Chemical class 0.000 description 4
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 3
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- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000003995 emulsifying agent Substances 0.000 description 3
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- 238000007046 ethoxylation reaction Methods 0.000 description 3
- 235000019439 ethyl acetate Nutrition 0.000 description 3
- 150000002191 fatty alcohols Chemical class 0.000 description 3
- 150000002576 ketones Chemical class 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- NBVXSUQYWXRMNV-UHFFFAOYSA-N monofluoromethane Natural products FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 3
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- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 3
- UWNADWZGEHDQAB-UHFFFAOYSA-N 2,5-dimethylhexane Chemical group CC(C)CCC(C)C UWNADWZGEHDQAB-UHFFFAOYSA-N 0.000 description 2
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- FOGYNLXERPKEGN-UHFFFAOYSA-N 3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfopropyl)phenoxy]propane-1-sulfonic acid Chemical compound COC1=CC=CC(CC(CS(O)(=O)=O)OC=2C(=CC(CCCS(O)(=O)=O)=CC=2)OC)=C1O FOGYNLXERPKEGN-UHFFFAOYSA-N 0.000 description 2
- 239000005995 Aluminium silicate Substances 0.000 description 2
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- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 2
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- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 2
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- 238000004090 dissolution Methods 0.000 description 2
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- 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 2
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 2
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- LZGUHMNOBNWABZ-UHFFFAOYSA-N n-nitro-n-phenylnitramide Chemical compound [O-][N+](=O)N([N+]([O-])=O)C1=CC=CC=C1 LZGUHMNOBNWABZ-UHFFFAOYSA-N 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
- 230000035764 nutrition Effects 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- JMJRYTGVHCAYCT-UHFFFAOYSA-N oxan-4-one Chemical compound O=C1CCOCC1 JMJRYTGVHCAYCT-UHFFFAOYSA-N 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- 235000020232 peanut Nutrition 0.000 description 1
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 description 1
- 125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000008048 phenylpyrazoles Chemical class 0.000 description 1
- PTMHPRAIXMAOOB-UHFFFAOYSA-N phosphoramidic acid Chemical class NP(O)(O)=O PTMHPRAIXMAOOB-UHFFFAOYSA-N 0.000 description 1
- UHZYTMXLRWXGPK-UHFFFAOYSA-N phosphorus pentachloride Chemical compound ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 description 1
- SIOXPEMLGUPBBT-UHFFFAOYSA-N picolinic acid Chemical compound OC(=O)C1=CC=CC=N1 SIOXPEMLGUPBBT-UHFFFAOYSA-N 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004307 pyrazin-2-yl group Chemical group [H]C1=C([H])N=C(*)C([H])=N1 0.000 description 1
- JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical compound O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 1
- 150000003217 pyrazoles Chemical class 0.000 description 1
- 125000002206 pyridazin-3-yl group Chemical group [H]C1=C([H])C([H])=C(*)N=N1 0.000 description 1
- 125000004940 pyridazin-4-yl group Chemical group N1=NC=C(C=C1)* 0.000 description 1
- 150000004892 pyridazines Chemical class 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- LOAUVZALPPNFOQ-UHFFFAOYSA-N quinaldic acid Chemical compound C1=CC=CC2=NC(C(=O)O)=CC=C21 LOAUVZALPPNFOQ-UHFFFAOYSA-N 0.000 description 1
- 235000013526 red clover Nutrition 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 125000003548 sec-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 230000011218 segmentation Effects 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 150000003456 sulfonamides Chemical class 0.000 description 1
- 150000003461 sulfonyl halides Chemical class 0.000 description 1
- YROXIXLRRCOBKF-UHFFFAOYSA-N sulfonylurea Chemical class OC(=N)N=S(=O)=O YROXIXLRRCOBKF-UHFFFAOYSA-N 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000013616 tea Nutrition 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000002769 thiazolinyl group Chemical group 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 239000011573 trace mineral Substances 0.000 description 1
- 235000013619 trace mineral Nutrition 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1
- 235000018322 upland cotton Nutrition 0.000 description 1
- 229940035893 uracil Drugs 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 235000020234 walnut Nutrition 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
Classifications
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or 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
- C07D231/18—One oxygen or sulfur atom
- C07D231/20—One oxygen atom attached in position 3 or 5
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/32—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D207/325—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms with substituted hydrocarbon radicals directly attached to the ring nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or 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
- C07D231/16—Halogen atoms or nitro radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/08—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D263/32—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D275/00—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings
- C07D275/02—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings not condensed with other rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/22—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/38—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/10—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing aromatic rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
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- C—CHEMISTRY; METALLURGY
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- 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
- C07D417/10—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 linked by a carbon chain containing aromatic rings
Abstract
本发明涉及式Ⅰ的亚苄基吡唑啉酮,其中取代基和符号n具有下列含意:R1是未取代或取代的C1-C6-烷基;R2是未取代或取代的C1-C6-烷基、未取代或取代的C1-C6-烷氧基、卤素、硝基、氰基;R3是氢、卤素、硝基、氰基、基团NR5R6、OCOR5、NR5COR6、CO2R5、-COSR5、-CONR5R6、C1-C4-烷氧基亚氨基烷基、C1-C6-烷基羰基、未取代或取代的C1-C6-烷基、未取代或取代的C1-C6-烷氧基、未取代或取代的C1-C6-烷硫基、未取代或取代的C2-C6-烯基、未取代或取代的C2-C6-炔基、未取代或取代的苯基、未取代或取代的苯氧基、可以含有至多4个氮原子和/或至多2个氧原子或硫原子作为环成员的未取代或取代的5-或6-元饱和或不饱和杂环;R4是C1-C6-烷基、C1-C4-卤代烷基;或R3和R4形成任选取代的饱和或不饱和2-或3-元桥,该桥可以含有一可以被氧化成亚砜或砜的硫原子;R5是氢或未取代或取代的C1-C6-烷基;R6是未取代或取代的C1-C6-烷基;R7是氢、C1-C6-烷基或C1-C4-卤代烷基;n是0、1或2;X是氢、氯或溴;其中所要求的这些化合物可以以反式或顺式形式或这些异构体的混合物的形式存在。
Description
本发明涉及式Ⅰ的亚苄基吡唑啉酮
其中取代基和符号n具有下列含意:
R7是未取代或取代的C1-C6-烷基;
R2是未取代或取代的C1-C6-烷基、未取代或取代的C1-C6-烷氧基、卤素、硝基、氰基;
R3是氢、卤素、硝基、氰基、基团NR5R6、OCOR5、NR5COR6、CO2R5、-COSR5、-CONR5R6、C1-C4-烷氧基亚氨基烷基、C1-C6-烷基羰基、未取代或取代的C1-C6-烷基、未取代或取代的C1-C6-烷氧基、未取代或取代的C1-C6-烷硫基、未取代或取代的C2-C6-烯基、未取代或取代的C2-C6-炔基、未取代或取代的苯基、未取代或取代的苯氧基、可以含有至多4个氮原子和/或至多2个氧原子或硫原子作为环成员的未取代或取代的5-或6-元饱和或不饱和杂环;
R4是C1-C6-烷基、C1-C4-卤代烷基;或
R3和R4形成任选取代的饱和或不饱和2-或3-元桥,该桥可以含有-可以被氧化成亚砜或砜的硫原子;
R5是氢或未取代或取代的C1-C6-烷基;
R6是未取代或取代的C1-C6-烷基;
R7是氢、C1-C6-烷基或C1-C4-卤代烷基;
n是0、1或2;
X是氢、氯或溴;
其中所要求保护的这些化合物可以以反式或顺式形式或这些异构体的混合物的形式存在。
另外,本发明还涉及包含式Ⅰ化合物的组合物,涉及式Ⅰ化合物和包含它的组合物防治有害植物的应用,涉及式Ⅱ的新颖苯甲酰吡唑和涉及制备化合物Ⅰ和Ⅱ的方法。
除草活性4-苯甲酰基吡唑公开于文献,例如EP-A 282 944或WO 96/26206。然而,迄今未描述4-苯甲酰基-5-氯吡唑。在EP-A 282 944中,只是一般性地提到使4-苯甲酰基-5-羟基吡唑与酰基氯反应可以产生4-苯甲酰基-5-氯吡唑。
亚苄基吡唑啉酮(其中的一些具有除草活性)公开于US 4 382 948和JP 61268670中。迄今所有结构在亚苄基吡唑啉酮的苯基部分具有非常特别的取代类型:在次甲基桥的对位,例如,总有氢或卤素或三氟甲基或硝基。
然而,现有技术化合物的除草性能及其与作物的相容性并不完全令人满意。本发明的目的是提供一种新颖的特别是具有改进性能的除草活性化合物。
我们发现,本发明的目的通过根据本发明的式Ⅰ亚苄基吡唑啉酮和其除草活性得以实现。
本发明还提供式Ⅰ化合物的立体异构体。纯的立体异构体及其混合物均包括在内。
式Ⅰ化合物可以以顺式或反式异构体存在,且取代于取代类型,可以含有一或多个手性中心。在此情况下,它们还可以以对映体或非对映体的混合物存在。本发明的对象包括纯异构体、对映体或非对映体及其混合物。
本发明的式Ⅰ亚苄基吡唑啉酮和式Ⅱ苯甲酰基吡唑可以如下制备:
式Ⅰa的亚苄基吡唑啉酮(X=氢)可以根据US 4 382 948中描述的方法,通过式Ⅲ的吡唑啉酮(其中基团R1和R7如上所定义)与式Ⅳ的取代的苯甲醛(其中基团R2至R4如上所定义)的诺文葛耳缩合反应合成。
另外,式Ⅰa例如由其中X是溴的式Ⅰ化合物的还原脱卤反应获得。
亚苄基吡唑啉酮Ⅰb(X=溴或氯)可以由如上描述的化合物Ⅰa,通过用溴或氯卤化,随后在碱存在下脱去卤化氢而制备。
亚苄基吡唑啉酮Ⅰb优选由式Ⅴ的酮与酰卤反应而获得,而式Ⅴ是已知的或可以类似于已知化合物制备(参见,DE-A 19709118.0和WO 96/26200)。
适合的酰卤是例如硫酰卤、碳酰卤或磷酰卤。为了用氯交换,优选是使用亚硫酰卤、光气、五氯化磷和特别优选三氯氧化磷。为了用溴交换,优选是使用三溴氧化磷。
反应可以以常规方式,在没有溶剂,或采用在反应条件下是惰性的溶剂的情况下进行。通常,可以通过加入低亲核性的碱,例如,吡啶、二甲基氨基吡啶或二甲基甲酰胺,控制反应的选择性。
反应温度通常是0℃至200℃,优选是50℃至140℃。
在此反应中,可以获得对新形成的双键而言的二种异构体的混合物。在此情况下,如果需要,这些异构体可以分离(例如通过结晶、萃取或色谱法)。
反应的副产物是化合物Ⅱ,它取决于取代类型和进行反应的方式,可以以较小、相似或较大的比例获得。许多这些化合物是新的,且作为除草活性化合物的前体来说是很有意义的(参见,例如EP-A 282 944)。
针对取代基R1-R7或作为苯环或杂环上的基团提到的有机分子部分代表单个基团成员个别罗列的集合概念。所有的烃链,即,所有的烷基、卤代烷基、环烷基、烷氧基、卤代烷氧基、烷基羰基、烯基、炔基部分可以是直链或支链。除非另有说明,卤代的取代基优选带有一至五个相同或不同的卤素原子。卤素在每一情况下是氟、氯、溴或碘。
其它的基团的实例是:-C1-C4-烷基和其它基团例如C1-C4-烷氧基、C1-C4-烷基羰基、C1-C4-烷硫基的烷基部分:甲基、乙基、正丙基、1-甲基乙基、丁基、1-甲基丙基、2-甲基丙基和1,1-二甲基乙基;C1-C6-烷基和其它基团如C1-C6-烷氧基、C1-C6-烷基羰基、C1-C6-烷硫基的烷基部分:如上提到的C1-C4-烷基,和戊基、1-甲基丁基、2-甲基丁基、3-甲基丁基、2,2-二甲基丙基、1-乙基丙基、己基、1,1-二甲基丙基、1,2-二甲基丙基、1-甲基戊基、2-甲基戊基、3-甲基戊基、4-甲基戊基、1,1-二甲基丁基、1,2-二甲基丁基、1,3-二甲基丁基、2,2-二甲基丁基、2,3-二甲基丁基、3,3-二甲基丁基、1-乙基丁基、2-乙基丁基、1,1,2-三甲基丙基、1-乙基-1-甲基丙基和1-乙基-3-甲基丙基;
-C1-C4-卤代烷基:部分或全部由氟、氯、溴和/或碘取代的如上所述的C1-C4-烷基,即,例如,氯甲基、二氯甲基、三氯甲基、氟甲基、二氟甲基、三氟甲基、氯氟甲基、二氯氟甲基、氯二氟甲基、2-氟乙基、2-氯乙基、2-溴乙基、2-碘乙基、2,2-二氟乙基、2,2,2-三氟乙基、2-氯-2-氟乙基、2-氯-2,2-二氟乙基、2,2-二氯-2-氟乙基、2,2,2-三氯乙基、五氟乙基、2-氟丙基、3-氟丙基、2,2-二氟丙基、2,3-二氟丙基、2-氯丙基、3-氯丙基、2,3-二氯丙基、2-溴丙基、3-溴丙基、3,3,3-三氟丙基、3,3,3-三氯丙基、2,2,3,3,3-五氟丙基、七氟丙基、1-(氟甲基)-2-氟乙基、1-(氯甲基)-2-氯乙基、1-(溴甲基)-2-溴乙基、4-氟丁基、4-氯丁基、4-溴丁基和九氟丁基;
-C1-C4-卤代烷氧基:部分或全部由氟、氯、溴和/或碘取代的如上所述的C1-C4-烷氧基,即,例如,氟甲氧基、二氟甲氧基、三氟甲氧基、氯二氟甲氧基、溴二氟甲氧基、2-氟乙氧基、2-氯乙氧基、2-溴乙氧基、2-碘乙氧基、2,2-二氟乙氧基、2,2,2-三氟乙氧基、2-氯-2-氟乙氧基、2-氯-2,2-二氟乙氧基、2,2-二氯-2-氟乙氧基、2,2,2-三氯乙氧基、五氟乙氧基、2-氟丙氧基、3-氟丙氧基、2-氯丙氧基、3-氯丙氧基、2-溴丙氧基、3-溴丙氧基、2,2-二氟丙氧基、2,3-二氟丙氧基、2,3-二氯丙氧基、3,3,3-三氟丙氧基、3,3,3-三氯丙氧基、2,2,3,3,3-五氟丙氧基、七氟丙氧基、1-(氟甲基)-2-氟乙氧基、1-(氯甲基)-2-氯乙氧基、1-(溴甲基)-2-溴乙氧基、4-氟丁氧基、4-氯丁氧基、4-溴丁氧基和九氟丁氧基;
-C2-C6-烯基,如乙烯基、丙-1-烯-1-基、丙-2-烯-1-基、1-甲基乙烯基、丁烯-1-基、丁烯-2-基、丁烯-3-基、1-甲基丙-1-烯-1-基、2-甲基丙-1-烯-1-基、1-甲基丙-2-烯-1-基、2-甲基丙-2-烯-1-基、戊烯-1-基、戊烯-2-基、戊烯-3-基、戊烯-4-基、1-甲基丁-1-烯-1-基、2-甲基丁-1-烯-1-基、3-甲基丁-1-烯-1-基、1-甲基丁-2-烯-1-基、2-甲基丁-2-烯-1-基、3-甲基丁-2-烯-1-基、1-甲基丁-3-烯-1-基、2-甲基丁-3-烯-1-基、3-甲基丁-3-烯-1-基、1,1-二甲基-丙-2-烯-1-基、1,2-二甲基丙-1-烯-1-基、1,2-二甲基-丙-2-烯-1-基、1-乙基丙-1-烯-2-基、1-乙基丙-2-烯-1-基、己-1-烯-1-基、己-2-烯-1-基、己-3-烯-1-基、己-4-烯-1-基、己-5-烯-1-基、1-甲基戊-1-烯-1-基、2-甲基戊-1-烯-1-基、3-甲基戊-1-烯-1-基、4-甲基戊-1-烯-1-基、1-甲基戊-2-烯-1-基、2-甲基戊-2-烯-1-基、3-甲基戊-2-烯-1-基、4-甲基戊-2-烯-1-基、1-甲基戊-3-烯-1-基、2-甲基戊-3-烯-1-基、3-甲基戊-3-烯-1-基、4-甲基戊-3-烯-1-基、1-甲基戊-4-烯-1-基、2-甲基戊-4-烯-1-基、3-甲基戊-4-烯-1-基、4-甲基戊-4-烯-1-基、1,1-二甲基丁-2-烯-1-基、1,1-二甲基丁-3-烯-1-基、1,2-二甲基丁-1-烯-1-基、1,2-二甲基丁-2-烯-1-基、1,2-二甲基丁-3-烯-1-基、1,3-二甲基丁-1-烯-1-基、1,3-二甲基丁-2-烯-1-基、1,3-二甲基丁-3-烯-1-基、2,2-二甲基丁-3-烯-1-基、2,3-二甲基丁-1-烯-1-基、2,3-二甲基丁-2-烯-1-基、2,3-二甲基丁-3-烯-1-基、3,3-二甲基丁-1-烯-1-基、3,3-二甲基丁-2-烯-1-基、1-乙基-丁-1-烯-1-基、1-乙基-丁-2-烯-1-基、1-乙基-丁-3-烯-1-基、2-乙基-丁-1-烯-1-基、2-乙基-丁-2-烯-1-基、2-乙基-丁-3-烯-1-基、1,1,2-三甲基丙-2-烯-1-基、1-乙基-1-甲基丙-2-烯-1-基、1-乙基-2-甲基丙-1-烯-1-基和1-乙基-2-甲基丙-2-烯-1-基;
-C2-C6-炔基,如;乙炔基、丙-1-炔-1-基、丙-2-炔-1-基、丁-1-炔-1-基、丁-1-炔-3-基、丁-1-炔-4-基、丁-2-炔-1-基、戊-1-炔-1-基、戊-1-炔-3-基、戊-1-炔-4-基、戊-1-炔-5-基、戊-2-炔-1-基、戊-2-炔-4-基、戊-2-炔-5-基、3-甲基丁-1-炔-3-基、3-甲基丁-1-炔-4-基、己-1-炔-1-基、己-1-炔-3-基、己-1-炔-4-基、己-1-炔-5-基、己-1-炔-6-基、己-2-炔-1-基、己-2-炔-4-基、己-2-炔-5-基、己-2-炔-6-基、己-3-炔-1-基、己-3-炔-2-基、3-甲基戊-1-炔-1-基、3-甲基戊-1-炔-3-基、3-甲基戊-1-炔-4-基、3-甲基戊-1-炔-5-基、4-甲基戊-1-炔-1-基、4-甲基戊-2-炔-4-基和4-甲基戊-2-炔-5-基;
-C3-C6-环烷基;环丙基、环丁基、环戊基和环己基;
-含有至多4个氮原子和/或至多2个氧或硫原子作为环成员的未取代或取代的5-或6-元饱和或不饱和杂环,如2-四氢呋喃基、3-四氢呋喃基、2-四氢噻吩基、3-四氢噻吩基、2-吡咯烷基、3-吡咯烷基、3-异噁唑烷基、4-异噁唑烷基、5-异噁唑烷基、3-异噻唑烷基、4-异噻唑烷基、5-异噻唑烷基、3-吡唑烷基、4-吡唑烷基、5-吡唑烷基、2-噁唑烷基、4-噁唑烷基、5-噁唑烷基、2-噻唑烷基、4-噻唑烷基、5-噻唑烷基、2-咪唑烷基、4-咪唑烷基、1,2,4-噁二唑烷-3-基、1,2,4-噁二唑烷-5-基、1,2,4-噻二唑烷-3-基、1,2,4-噻二唑烷-5-基、1,2,4-三唑烷-3-基、1,3,4-噁二唑烷-2-基、1,3,4-噻二唑烷-2-基、1,3,4-三唑烷-2-基、2,3-二氢呋喃-2-基、2,3-二氢呋喃-3-基、2,3-二氢呋喃-4-基、2,3-二氢呋喃-5-基、2,5-二氢呋喃-2-基、2,5-二氢呋喃-3-基、2,3-二氢噻吩-2-基、2,3-二氢噻唑-3-基、2,3-二氢噻吩-4-基、2,3-二氢噻吩-5-基、2,5-二氢噻吩-2-基、2,5-二氢噻吩-3-基、2,3-二氢吡咯-2-基、2,3-二氢吡咯-3-基、2,3-二氢吡咯-4-基、2,3-二氢吡咯-5-基、2,5-二氢吡咯-2-基、2,5-二氢吡咯-3-基、2,3-二氢异噁唑-3-基、2,3-二氢异噁唑-4-基、2,3-二氢异噁唑-5-基、4,5-二氢异噁唑-3-基、4,5-二氢异噁唑-4-基、4,5-二氢异噁唑-5-基、2,5-二氢异噁唑-3-基、2,5-二氢异噁唑-4-基、2,5-二氢噁唑-5-基、2,3-二氢异噻唑-3-基、2,3-二氢异噻唑-4-基、2,3-二氢异噻唑-5-基、4,5-二氢异噻唑-3-基、4,5-二氢异噻唑-4-基、4,5-二氢异噻唑-5-基、2,5-二氢异噻唑-3-基、2,5-二氢异噻唑-4-基、2,5-二氢异噻唑-5-基、2,3-二氢吡唑-3-基、2,3-二氢吡唑-4-基、2,3-二氢吡唑-5-基、4,5-二氢吡唑-3-基、4,5-二氢吡唑-4-基、4,5-二氢吡唑-5-基、2,5-二氢吡唑-3-基、2,5-二氢吡唑-4-基、2,5-二氢吡唑-5-基、2,3-二氢噁唑-2-基、2,3-二氢噁唑-4-基、2,3-二氢噁唑-5-基、4,5-二氢唑-2-基、4,5-二氢噁唑-4-基、4,5-二氢噁唑-5-基、2,5-二氢噁唑-2-基、2,5-二氢噁唑-4-基、2,5-二氢噁唑-5-基、2,3-二氢噻唑-2-基、2,3-二氢噻唑-4-基、2,3-二氢噻唑-5-基、4,5-二氢噻唑-2-基、4,5-二氢噻唑-4-基、4,5-二氢噻唑-5-基、2,5-二氢噻唑-2-基、2,5-二氢噻唑-4-基、2,5-二氢噻唑-5-基、2,3-二氢咪唑-2-基、2,3-二氢咪唑-4-基、2,3-二氢咪唑-5-基、4,5-二氢咪唑-2-基、4,5-二氢咪唑-4-基、4,5-二氢咪唑-5-基、2,5-二氢咪唑-2-基、2,5-二氢咪唑-4-基、2,5-二氢咪唑-5-基、2-吗啉基、3-吗啉基、2-哌啶基、3-哌啶基、4-哌啶基、3-四氢哒嗪基、4-四氢哒嗪基、2-四氢嘧啶基、4-四氢嘧啶基、5-四氢嘧啶基、2-四氢吡嗪基、1,3,5-四氢三嗪-2-基、1,2,4-四氢三嗪-3-基、1,3-二氢噁嗪-2-基、1,3-二噻烷-2-基、2-四氢吡喃基、3-四氢吡喃基、4-四氢吡喃基、2-四氢噻喃基、3-四氢噻喃基、4-四氢噻喃基、1,3-二氧戊烷-2-基、3,4,5,6-四氢吡啶-2-基、4H-1,3-噻嗪-2-基、4H-,1,1-二氧代-2,3,4,5-四氢噻吩-2-基、1,3-二氢噁嗪-2-基、2-呋喃基、3-呋喃基、2-噻吩基、3-噻吩基、2-吡咯基、3-吡咯基、3-异噁唑基、4-异噁唑基、5-异噁唑基、3-异噻唑基、4-异噻唑基、5-异噻唑基、3-吡唑基、4-吡唑基、5-吡唑基、2-噁唑基、4-噁唑基、5-噁唑基、2-噻唑基、四唑-5-基、四唑-1-基、4-噻唑基、5-噻唑基、2-咪唑基、4-咪唑基、1,2,4-噁二唑-3-基、1,2,4-噁二唑-5-基、1,2,4-噻二唑-3-基、1,2,4-噻二唑-5-基、1,2,4-三唑-3-基、1,3,4-噁二唑-2-基、1,3,4-噻二唑-2-基、1,3,4-三唑-2-基、2-吡啶基、3-吡啶基、4-吡啶基、3-哒嗪基、4-哒嗪基、2-嘧啶基、4-嘧啶基、5-嘧啶基、2-吡嗪基、1,3,5-三嗪-2-基、1,2,4-三嗪-3-基、1,2,4,5-四嗪-3-基。
对于本发明亚苄基吡唑Ⅰ的除草活性而言,特别优选的是在每一种情况下可以是单独的或是组合的下列取代基含意:R1是C1-C4-烷基或C1-C4-卤代烷基;R2是C1-C4-烷基、C1-C4-卤代烷基、C1-C4-烷氧基、C1-C4
-卤代烷氧基、卤素、硝基、氰基;R3是氢、卤素、硝基、氰基、基团NR5R6、OCOR5、NR5COR6、CO2R5、
-COSR5、-CONR5R5、C1-C4-烷氧基亚氨基烷基、C1-C4-烷
基羰基、未取代或由卤素、C1-C4-烷氧基或苯基取代的C1-C4
-烷基,其中,苯环本身可以由卤素、C1-C2-烷基或C1-C2-烷氧基取代,未取代或由卤素、C1-C4-烷氧基或苯基取代的C1-C4-烷氧基,其中苯环本身可以由卤素、C1-C2-烷基或C1-C2-烷氧基-取代,未取代或由卤素、C1-C4-烷氧基或苯基取代的C1-C4-烷硫基,其中苯环本身可以由卤素、C1-C2-烷基或C1-C2-烷氧基-取代,未取代或由C1-C4-烷基或卤素取代的C2-C6-烯基或C2-C6-炔基、未取代或由C1-C4-烷基、C1-C4-烷氧基、C1-C4-卤代烷基、C1-C4-卤代烷氧基、卤素、苯基、氰基、烷氧羰基或硝基取代的苯基或苯氧基,未取代或由C1-C4-烷基,C1-C4-烷氧基,C1-C4-卤代烷基,C1-C4卤代烷氧基,卤素、苯基、氰基或硝基取代的5-或6-元饱和或不饱和杂环,该杂环可以含有至多4个氮原子和/或至多2个氧或硫原子作为环成员,所述的杂环选自下列基团:四氢呋喃基、四氢噻吩基、吡咯烷基、异噁唑烷基、异噻唑烷基、吡唑烷基、唑烷基、噻唑烷基、咪唑烷基、1,2,4-噁二唑烷基、1,2,4-噻二唑烷基、1,2,4-三唑烷基、1,3,4-二唑烷基、1,3,4-噻二唑烷基、1,3,4-三唑烷基、2,3-二氢呋喃基、2,5-二氢呋喃基、2,3-二氢噻吩基、2,5-二氢噻吩基、2,3-二氢吡咯基、2,5-二氢吡咯基、2,3-二氢异噁唑基、4,5-二氢异噁唑基、2,5-二氢异噁唑基、2,5-二氢噁唑基、2,3-二氢异噻唑基、4,5-二氢异噻唑基、2,5-二氢异噻唑基、2,3-二氢吡唑基、4,5-二氢吡唑基、2,5-二氢吡唑基、2,3-二氢噁唑基、4,5-二氢噁唑基、2,5-二氢噁唑基、2,3-二氢噻唑基、4,5-二氢噻唑基、2,5-二氢噻唑基、2,3-二氢咪唑基、4,5-二氢咪唑基、2,5-二氢咪唑基、吗啉基、哌啶基、四氢哒嗪基、四氢嘧啶基、四氢吡嗪基、1,3,5-四氢三嗪基、1,2,4-四氢三嗪基、1,3-二氢噁嗪基、1,3-二噻烷基、四氢吡喃基、四氢噻喃基、1,3-二氧戊环基、1,1-二氧代-2,3,4,5-四氢噻吩基、1,3-二氢噁嗪基、呋喃基、噻吩基、吡咯基、异噁唑基、异噻唑基、吡唑基、噁唑基、噻唑基、咪唑基、1,2,4-噁二唑基、1,2,4-噻二唑基、1,2,4-三唑基、四唑基、1,3,4-噁二唑基、1,3,4-噻二唑基、1,3,4-三唑基、吡啶基、哒嗪基、嘧啶基、吡嗪基、1,3,5-三嗪基、1,2,4-三嗪基、1,2,4,5-四嗪基;
R4是C1-C6-烷基、C1-C4-卤代烷基;或
R3和R4形成未取代或取代的饱和或不饱和2-或3-元桥,该桥可以含有一个可以氧化成亚砜或砜的硫原子,
R5是氢、C1-C4-烷基,该烷基是未取代的或由卤素、C1-C4-烷氧基或苯基取代,其中苯环可以带有一至五个选自卤素、C1-C2-烷基和C1-C2-烷氧基的取代基;
R6是C1-C4-烷基,该烷基是未取代的或由卤素、C1-C4-烷氧基或苯基取代,其中苯环可以带有一至五个选自卤素、C1-C2-烷基和C1-C2-烷氧基的取代基;
R7是氢、C1-C4-烷基或C1-C4-卤代烷基;n是0、1或2;X是氢、氯或溴;
其中所要求保护的这些化合物可以以反式和顺式构形或这些异构体的混合物的形式存在。
优选的是这样的苯环或杂环,它们是未取代或带有一至三个卤原子和/或一或二个选自下列的基团:硝基、氰基、甲基、乙基、三氟甲基、甲氧基、乙氧基和三氟甲氧基。
特别优选的是这样的表1式Ⅰ化合物,其中取代基可以具有在每一种情况下可以是单独的或是组合的下列取代基含意:R1是甲基、乙基;R2是氯、甲基、甲氧基;R3是氢、甲基、未取代的苄基或在苯环部分由氟-、氯-、甲基
-或甲氧基取代的苄基、烯丙基、丙炔-3-基、甲氧基、乙氧
基、2-甲氧基乙氧基、甲硫基、甲基羰基、甲氧基羰基、二甲基氨基羰基、氰基;优选未取代或由氟-、氯-、甲基-或甲氧基-取代的苯基、2-呋喃基、3-呋喃基、2-噻吩基、3-噻吩基、4,5-二氢异噁唑-3-基、异噁唑-5-基、异噁唑-3-基、吡唑-1-基、吡唑-5-基、噁唑-2-基、4,5-二氢噁唑-2-基、1,3-二氧戊环-2-基、1,3-二硫戊环-2-基、噻唑-2-基、噻唑-5-基、噻唑-4-基、[1,2,4]-三唑-1-基、[1,3,4]-噁二唑-2-基、2-吡啶基、3-吡啶基、4-吡啶基、嘧啶-2-基、嘧啶-4-基、1,3-二噁烷-2-基、1,3-二噻烷-2-基;
R4是甲基;
R7是氢;
n是2;
X是氯。
其中R3是未取代或取代的5-或6-元饱和或不饱和杂环的式Ⅱ苯甲酰吡唑是新的。特别适合于用作制备德国专利申请DE19740494.4中描述的除草活性化合物的中间体的式Ⅱ苯甲酰吡唑是那些其中取代基具有下列含意的化合物:
R1是C1-C4-烷基或C1-C4-卤代烷基;
R2是C1-C4-烷基、C1-C4-卤代烷基、C1-C4-烷氧基、C1-C4-卤代烷氧基、卤素;
R3是未取代或由C1-C4-烷基、C1-C4-烷氧基、C1-C4-卤代烷基、C1-C4-卤代烷氧基或卤素取代的选自下列的5-或6-元饱和或不饱和杂环:四氢呋喃基、四氢噻吩基、吡咯烷基、异噁唑烷基、异噻唑烷基、吡唑烷基、唑烷基、噻唑烷基、咪唑烷基、1,2,4-噁二唑烷基、1,2,4-噻二唑烷基、1,2,4-三唑烷基、1,3,4-噁二唑烷基、1,3,4-噻二唑烷基、1,3,4-三唑烷基、2,3-二氢呋喃基、2,5-二氢呋喃基、2,3-二氢噻吩基、2,5-二氢噻吩基、2,3-二氢吡咯基、2,5-二氢吡咯基、2,3-二氢异噁唑基、4,5-二氢异噁唑基、2,5-二氢异噁唑基、2,5-二氢噁唑基、2,3-二氢异噻唑基、4,5-二氢异噻唑基、2,5-二氢异噻唑基、2,3-二氢吡唑基、4,5-二氢吡唑基、2,5-二氢吡唑基、2,3-二氢噁唑基、4,5-二氢噁唑基、2,5-二氢噁唑基、2,3-二氢噻唑基、4,5-二氢噻唑基、2,5-二氢噻唑基、2,3-二氢咪唑基、4,5-二氢咪唑基、2,5-二氢咪唑基、吗啉基、哌啶基、四氢哒嗪基、四氢嘧啶基、四氢吡嗪基、1,3,5-四氢三嗪基、1,2,4-四氢三嗪基、1,3-二氢噁嗪基、1,3-二噻烷基、四氢吡喃基、四氢噻喃基、1,3-二氧戊环基、1,1-二氧代-2,3,4,5-四氢噻吩基、1,3-二氢噁嗪基、呋喃基、噻吩基、吡咯基、异噁唑基、异噻唑基、吡唑基、噁唑基、噻唑基、咪唑基、1,2,4-噁二唑基、1,2,4-噻二唑基、1,2,4-三唑基、四唑基、1,3,4-噁二唑基、1,3,4-噻二唑基、1,3,4-三唑基、吡啶基、哒嗪基、嘧啶基、吡嗪基、1,3,5-三嗪基、1,2,4-三嗪基、1,2,4,5-四嗪基;特别优选是:2-呋喃基、3-呋喃基、2-噻吩基、3-噻吩基、4,5-二氢异噁唑-3-基、异噁唑-5-基、异噁唑-3-基、吡唑-1-基、吡唑-5-基、噁唑-2-基、4,5-二氢噁唑-2-基、1,3-二氧戊环-2-基、1,3-二硫戊环-2-基、噻唑-2-基、噻唑-5-基、噻唑-4-基、[1,2,4]-三唑-1-基、[1,3,4]-噁二唑-2-基、2-吡啶基、3-吡啶基、4-吡啶基、嘧啶-2-基、嘧啶-4-基、1,3-二噁烷-2-基、1,3-二噻烷-2-基;
R4是C1-C4-烷基或C1-C4-卤代烷基;
R7是氢、C1-C4-烷基或C1-C4-卤代烷基;
n是0、1或2;
X是氯或溴。
特别优选的是表2中的式Ⅱ化合物。
制备实施例:
1)顺-4-[氯(2-氯-3-(4,5-二氢异噁唑-3-基)-4-甲基磺酰基苯基)亚甲基]-2-甲基-2,4-二氢吡唑-3-酮(表1化合物Ⅰ.20):将在15ml甲苯中的5.0g(2-氯-3-(4,5-二氢异噁唑-3-基)-4-甲基磺酰基苯基)(5-羟基-1-甲基-1H-吡唑-4-基)-甲酮与2.0g三氯氧化磷和2滴二甲基甲酰胺混合,并加热回流74时。再加入1.0g三氯氧化磷,并将此混合物再加热回流7小时。之后将反应混合物加入到125ml冰-水中,并用甲基叔丁基醚萃取。粗制的产物经硅胶使用环己烷/乙酸乙酯/甲醇色谱纯化。产量:1.3g无色固体(顺式异构体)。1H NMR(CDCl3):d=3.27(s);3.31(s);3.45(t);4.57(t);7.65(d);7.73(s);8.15(d)。
另外,在反应混合物的色谱纯化期间分离出异构的苯甲酰吡唑:(5-氯-1-甲基吡唑-4-基)-(2-氯-3-(4,5-二氢异噁唑-3-基)-4-甲基磺酰基苯基)-3-甲酮(表2化合物Ⅱ.17):
1H-NMR(CDCl3):d=3,30(s);3,45(t);3,93(s)4,63(t);7,61(d);7,75(s);8,17(d)。
2)顺-4-[氯(2-氯-3-(4,5-二氢异噁唑-3-基)-4-甲基磺酰基苯基)亚甲基]-2-乙基-2,4-二氢吡唑-3-酮(表1化合物Ⅰ.119):
此化合物可以类似于实施例1的方法制备。无色固体(顺式异构体);
1H-NMR(CDCl3):d=1,28(t);3,27(s)3.46(t);3,72(q),4,62(t);7,64(d);7,73(s);8.16(d).
另外,在反应混合物的色谱纯化期间分离出异构的苯甲酰吡唑:(5-氯-1-乙基吡唑-4-基)-(2-氯-3-(4,5-二氢异噁唑-3-基)-4-甲基磺酰基苯基)甲酮(表2化合物Ⅱ.56):
1H-NMR(CDCl3):d=1,50(t);3,28(s);3,45(t);4,28(q),4,63(t);7,63(d);7,74(s);8,18(d)。
3)顺-4-[溴(2-氯-3-(4,5-二氢异噁唑-3-基)-4-甲基磺酰基苯基)亚甲基]-2-甲基-2,4-二氢吡唑-3-酮(表1化合物Ⅰ.466):
将在20ml甲苯中的2.5g(2-氯-3-(4,5-二氢异噁唑-3-基)-4-甲基磺酰基苯基)(5-羟基-1-甲基-1H-吡唑-4-基)-甲酮与1.87g三溴氧化磷和2滴二甲基甲酰胺混合,并加热回流13小时。之后将反应混合物倒入50℃碳酸钠溶液中,并用甲基叔丁基醚萃取。粗制的产物经硅胶使用环己烷/乙酸乙酯/甲醇色谱纯化。1H-NMR(CDCl3):d=3,25(s);3,31(s);3,43(m);4,59(t);7,57(d);7,63(s);8,15(d)。
列于下文表1和2中的式Ⅰ亚苄基吡唑啉酮和式Ⅱ苯甲酰吡唑可以通过类似于上面合成实施例中给出的方法合成。
表1:
Nr. | R1 | R2 | R3 | R4 | R7 | X | n | 异构体 | 物理数据 |
Ⅰ.1 | CH3 | Cl | H | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.2 | CH3 | Cl | F | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.3 | CH3 | Cl | Cl | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.4 | CH3 | Cl | Br | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.5 | CH3 | Cl | CH3 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.6 | CH3 | Cl | CF3 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.7 | CH3 | Cl | CHF2 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.8 | CH3 | Cl | 乙基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.9 | CH3 | Cl | 异丙基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.10 | CH3 | Cl | 苄基 | CH3 | H | Cl | 2 | 顺式 |
Nr. | R1 | R2 | R3 | R4 | R7 | X | n | 异构体 | 物理数据 |
Ⅰ.11 | CH3 | Cl | 4-氯苯基甲基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.12 | CH3 | Cl | 烯丙基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.13 | CH3 | Cl | 反式-氯烯丙基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.14 | CH3 | Cl | 顺式-氯烯丙基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.15 | CH3 | Cl | 顺式-2-氯乙烯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.16 | CH3 | Cl | 反式-2-氯乙烯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.17 | CH3 | Cl | 2,2-二氯乙烯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.18 | CH3 | Cl | 丙炔-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.19 | CH3 | Cl | 乙炔基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.20 | CH3 | Cl | 4,5-二氢异噁唑-3-基 | CH3 | H | Cl | 2 | 顺式 | 参见实施例1 |
Ⅰ.2l | CH3 | Cl | 异噁唑-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.22 | CH3 | Cl | 3-甲基异噁唑-5-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.23 | CH3 | Cl | 4-甲基-4,5-二氢异噁唑-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.24 | CH3 | Cl | 3-乙基-4,5-二氢异噁唑-4-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.25 | CH3 | Cl | 3-乙基-4,5-二氢异噁唑-5-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.26 | CH3 | Cl | 5-甲基-4,5-二氢异噁唑-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.27 | CH3 | Cl | 4,5-二甲基-4,5-二氢异噁唑-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.28 | CH3 | Cl | 噻唑-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.29 | CH3 | Cl | 5-甲基噻唑-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.30 | CH3 | Cl | 噻唑-4-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.31 | CH3 | Cl | 噻唑-5-基 | CH3 | H | Cl | 2 | 顺式 |
Nr. | R1 | R2 | R3 | R4 | R7 | X | n | 异构体 | 物理数据 |
Ⅰ.32 | CH3 | Cl | 噁唑-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.33 | CH3 | Cl | 4,5-二氢噁唑-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.34 | CH3 | Cl | 吡咯-1-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.35 | CH3 | Cl | 吡唑-1-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.36 | CH3 | Cl | 1-甲基吡唑-5-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.37 | CH3 | Cl | 1-甲基吡唑-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.38 | CH3 | Cl | 1-甲氧基吡唑-5-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.39 | CH3 | Cl | 1-甲氧基吡唑-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.40 | CH3 | Cl | 1-甲基咪唑-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.41 | CH3 | Cl | 咪唑-1-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.42 | CH3 | Cl | [1,2,4]-三唑-1-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.43 | CH3 | Cl | 1-甲基-[1,2,4]-三唑-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.44 | CH3 | Cl | 2-噻吩基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.45 | CH3 | Cl | 3-噻吩基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.4 6 | CH3 | Cl | 四氢噻喃-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.47 | CH3 | Cl | 四氢噻喃-4-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.48 | CH3 | Cl | [1,3]二硫戊环-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.49 | CH3 | Cl | 2-呋喃基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.50 | CH3 | Cl | 3-呋喃基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.51 | CH3 | Cl | 四氢呋喃-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.52 | CH3 | Cl | 四氢呋喃-3-基 | CH3 | H | Cl | 2 | 顺式 |
Nr. | R1 | R2 | R3 | R4 | R7 | X | n | 异构体 | 物理数据 |
Ⅰ.53 | CH3 | Cl | [1,3]-二氧戊环-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.54 | CH3 | Cl | 四氢吡喃-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.55 | CH3 | Cl | 四氢吡喃-4-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.56 | CH3 | Cl | [1,3]-二噁烷-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.57 | CH3 | Cl | [1,3,4]-恶二唑-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.58 | CH3 | Cl | 哌啶-1-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.59 | CH3 | Cl | 2-吡啶基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.60 | CH3 | Cl | 6-甲氧基-2-吡啶基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.61 | CH3 | Cl | 5-三氟甲基-2-吡啶基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.62 | CH3 | Cl | 2-氯-5-三氟甲基-2-吡啶基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.63 | CH3 | Cl | 3-吡啶基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.64 | CH3 | Cl | 4-吡啶基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.65 | CH3 | Cl | 吗啉-4-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.66 | CH3 | Cl | 嘧啶-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.67 | CH3 | Cl | 嘧啶-4-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.68 | CH3 | Cl | 吡嗪-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.69 | CH3 | Cl | 哒嗪-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.70 | CH3 | Cl | 哒嗪-4-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.71 | CH3 | Cl | 6-甲基哒嗪-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.72 | CH3 | Cl | 6-甲氧基哒嗪-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.73 | CH3 | Cl | [1,3,5]-三嗪-2-基 | CH3 | H | Cl | 2 | 顺式 |
Nr. | R1 | R2 | R3 | R4 | R7 | X | n | 异构体 | 物理数据 |
Ⅰ.74 | CH3 | Cl | [1,2,4]-三嗪-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.75 | CH3 | Cl | 苯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.76 | CH3 | Cl | 2-氟苯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.77 | CH3 | Cl | 3-三氟甲基苯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.78 | CH3 | Cl | 2-甲基苯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.79 | CH3 | Cl | 3-甲基苯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.80 | CH3 | Cl | 4-甲基苯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.81 | CH3 | Cl | 4-氯苯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.82 | CH3 | Cl | 2-氯苯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.83 | CH3 | Cl | 3-氯苯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.84 | CH3 | Cl | 4-甲氧基苯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.85 | CH3 | Cl | 甲硫基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.86 | CH3 | Cl | 甲氧基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.87 | CH3 | Cl | 乙氧基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.88 | CH3 | Cl | 2-甲氧基乙氧基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.89 | CH3 | Cl | 甲酰基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.90 | CH3 | Cl | 乙酰基氨基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.91 | CH3 | Cl | 甲基羰基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.92 | CH3 | Cl | 甲氧基羰基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.93 | CH3 | Cl | 二甲基氨基羰基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.94 | CH3 | Cl | 甲氧基亚氨基甲基 | CH3 | H | Cl | 2 | 顺式 |
Nr. | R1 | R2 | R3 | R4 | R7 | X | n | 异构体 | 物理数据 |
Ⅰ.95 | CH3 | Cl | 乙氧基亚氨基甲基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.96 | CH3 | Cl | 1-乙氧基亚氨基乙基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.97 | CH3 | Cl | 1-甲氧基亚氨基乙基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.98 | CH3 | Cl | 1-乙氧基亚氨基丙基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.99 | CH3 | Cl | 1-甲氧基亚氨基丙基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.100 | CH3 | Cl | 氰基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.101 | C2H5 | Cl | H | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.102 | C2H5 | Cl | Cl | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.103 | C2H5 | Cl | Br | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.104 | C2H5 | Cl | CH3 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.105 | C2H5 | Cl | CF3 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.106 | C2H5 | Cl | CHF2 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.107 | C2H5 | Cl | 乙基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.108 | C2H5 | Cl | 异丙基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.109 | C2H5 | Cl | 苄基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.110 | C2H5 | Cl | 4-氯苯基甲基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.111 | C2H5 | Cl | 烯丙基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.112 | C2H5 | Cl | 反式-氯烯丙基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.113 | C2H5 | Cl | 顺式-氯烯丙基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.114 | C2H5 | Cl | 顺式-2-氯乙烯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.115 | C2H5 | Cl | 反式-2-氯乙烯基 | CH3 | H | Cl | 2 | 顺式 |
No. | R1 | R2 | R3 | R4 | R7 | X | n | 异构体 | 物理数据 |
Ⅰ.116 | C2H5 | Cl | 2,2-二氯乙烯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.117 | C2H5 | Cl | 丙炔-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.118 | C2H5 | Cl | 乙炔基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.119 | C2H5 | Cl | 4,5-二氢异噁唑-3-基 | CH3 | H | Cl | 2 | 顺式 | 参见实施例2 |
Ⅰ.120 | C2H5 | Cl | 异噁唑-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.121 | C2H5 | Cl | 3-甲基异噁唑-5-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.122 | C2H5 | Cl | 4-甲基-4,5-二氢异噁唑-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.123 | C2H5 | Cl | 3-乙基-4,5-二氢异噁唑-4-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.124 | C2H5 | Cl | 3-乙基-4,5-二氢异噁唑-5-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.125 | C2H5 | Cl | 5-甲基-4,5-二氢异噁唑-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.126 | C2H5 | Cl | 4,5-二甲基-4,5-二氢异噁唑-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.127 | C2H5 | Cl | 噻唑-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.128 | C2H5 | Cl | 5-甲基噻唑-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.129 | C2H5 | Cl | 噻唑-4-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.130 | C2H5 | Cl | 噻唑-5-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.13l | C2H5 | Cl | 噁唑-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.132 | C2H5 | Cl | 4,5-二氢噁唑-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.133 | C2H5 | Cl | 吡咯-1-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.134 | C2H5 | Cl | 吡唑-1-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.135 | C2H5 | Cl | 1-甲基吡唑-5-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.136 | C2H5 | Cl | 1-甲基吡唑-3-基 | CH3 | H | Cl | 2 | 顺式 |
Nr. | R1 | R2 | R3 | R4 | R7 | X | n | 异构体 | 物理数据 |
Ⅰ.137 | C2H5 | Cl | 1-甲氧基吡唑-5-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.138 | C2H5 | Cl | 1-氧基吡唑-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.139 | C2H5 | Cl | 1-甲基咪唑-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.140 | C2H5 | Cl | 咪唑-1-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.141 | C2H5 | Cl | [1,2,4]-三唑-1-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.142 | C2H5 | Cl | 1-甲基-[1,2,4]-三唑-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.143 | C2H5 | Cl | 2-噻吩基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.144 | C2H5 | Cl | 3-噻吩基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.145 | C2H5 | Cl | 四氢噻喃-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.146 | C2H5 | Cl | 四氢噻喃-4-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.147 | C2H5 | Cl | [1,3]二硫戊环-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.148 | C2H5 | Cl | 2-呋喃基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.149 | C2H5 | Cl | 3-呋喃基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.150 | C2H5 | Cl | 四氢呋喃-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.15l | C2H5 | Cl | 四氢呋喃-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.152 | C2H5 | Cl | [1,3]-二氧戊环-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.153 | C2H5 | Cl | 四氢吡喃-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.154 | C2H5 | Cl | 四氢吡喃-4-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.155 | C2H5 | Cl | [1,3]-二噁烷-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.156 | C2H5 | Cl | [1,3,4]-噁二唑-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.157 | C2H5 | Cl | 哌啶-1-基 | CH3 | H | Cl | 2 | 顺式 |
No. | R1 | R2 | R3 | R4 | R7 | X | n | 异构体 | 物理数据 |
Ⅰ.158 | C2H5 | Cl | 2-吡啶基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.159 | C2H5 | Cl | 6-甲氧基-2-吡啶基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.160 | C2H5 | Cl | 5-三氟甲基-2-吡啶基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.161 | C2H5 | Cl | 2-氯-5-三氟甲基-2-吡啶基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.162 | C2H5 | Cl | 3-吡啶基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.163 | C2H5 | Cl | 4-吡啶基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.164 | C2H5 | Cl | 吗啉-4-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.165 | C2H5 | Cl | 嘧啶-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.166 | C2H5 | Cl | 嘧啶-4-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.167 | C2H5 | Cl | 吡嗪-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.168 | C2H5 | Cl | 哒嗪-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.169 | C2H5 | Cl | 哒嗪-4-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.170 | C2H5 | Cl | 6-甲基哒嗪-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.171 | C2H5 | Cl | 6-甲氧基哒嗪-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.172 | C2H5 | Cl | [1,3,5]-三嗪-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.173 | C2H5 | Cl | [1,2,4]-三嗪-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.174 | C2H5 | Cl | 苯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.175 | C2H5 | Cl | 2-氟苯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.176 | C2H5 | Cl | 3-三氟甲基苯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.177 | C2H5 | Cl | 2-甲基苯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.178 | C2H5 | Cl | 3-甲基苯基 | CH3 | H | Cl | 2 | 顺式 |
No. | R1 | R2 | R3 | R4 | R7 | X | n | 异构体 | 物理数据 |
Ⅰ.179 | C2H5 | Cl | 4-甲基苯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.180 | C2H5 | Cl | 4-氯苯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.18l | C2H5 | Cl | 2-氯苯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.182 | C2H5 | Cl | 3-氯苯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.183 | C2H5 | Cl | 4-甲氧基苯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.184 | C2H5 | Cl | 甲硫基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.185 | C2H5 | Cl | 甲氧基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.186 | C2H5 | Cl | 乙氧基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.187 | C2H5 | Cl | 2-甲氧基乙氧基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.188 | C2H5 | Cl | 甲酰基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.189 | C2H5 | Cl | 乙酰基氨基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.190 | C2H5 | Cl | 甲基羰基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.191 | C2H5 | Cl | 甲氧基羰基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.192 | C2H5 | Cl | 二甲基氨基羰基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.193 | C2H5 | Cl | 甲氧基亚氨基甲基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.194 | C2H5 | Cl | 乙氧基亚氨基甲基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.195 | C2H5 | Cl | 1-乙氧基亚氨基乙基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.196 | C2H5 | Cl | 1-甲氧基亚氨基乙基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.197 | C2H5 | Cl | 1-乙氧基亚氨基丙基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.198 | C2H5 | Cl | 1-甲氧基亚氨基丙基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.199 | C2H5 | Cl | 氰基 | CH3 | H | Cl | 2 | 顺式 |
No. | R1 | R2 | R3 | R4 | R7 | X | n | 异构体 | 物理数据 |
Ⅰ.200 | CH3 | CH3 | H | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.201 | CH3 | CH3 | F | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.202 | CH3 | CH3 | Cl | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.203 | CH3 | CH3 | Br | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.204 | CH3 | CH3 | CH3 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.205 | CH3 | CH3 | CF3 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.206 | CH3 | CH3 | CHF2 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.207 | CH3 | CH3 | 乙基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.208 | CH3 | CH3 | 异丙基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.209 | CH3 | CH3 | 苄基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.210 | CH3 | CH3 | 4-氯苯基甲基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.211 | CH3 | CH3 | 烯丙基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.212 | CH3 | CH3 | 反式-氯烯丙基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.213 | CH3 | CH3 | 顺式-氯烯丙基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.214 | CH3 | CH3 | 顺式-2-氯乙烯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.215 | CH3 | CH3 | 反式-2-氯乙烯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.216 | CH3 | CH3 | 2,2-二氯乙烯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.217 | CH3 | CH3 | 丙炔-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.218 | CH3 | CH3 | 乙炔基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.219 | CH3 | CH3 | 4,5-二氢异噁唑-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.220 | CH3 | CH3 | 异噁唑-3-基 | CH3 | H | Cl | 2 | 顺式 |
No. | R1 | R2 | R3 | R4 | R7 | X | n | 异构体 | 物理数据 |
Ⅰ.22l | CH3 | CH3 | 3-甲基异噁唑-5-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.222 | CH3 | CH3 | 4-甲基-4,5-二氢异噁唑-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.223 | CH3 | CH3 | 3-乙基-4,5-二氢异噁唑-4-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.224 | CH3 | CH3 | 3-乙基-4,5-二氢异噁唑-5-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.225 | CH3 | CH3 | 5-甲基-4,5-二氢异噁唑-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.226 | CH3 | CH3 | 4,5-二甲基-4,5-二氢异噁唑-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.227 | CH3 | CH3 | 噻唑-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.228 | CH3 | CH3 | 5-甲基噻唑-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.229 | CH3 | CH3 | 噻唑-4-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.230 | CH3 | CH3 | 噻唑-5-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.231 | CH3 | CH3 | 噁唑-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.232 | CH3 | CH3 | 4,5-二氢噁唑-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.233 | CH3 | CH3 | 吡咯-1-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.234 | CH3 | CH3 | 吡唑-1-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.235 | CH3 | CH3 | 1-甲基吡唑-5-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.236 | CH3 | CH3 | 1-甲基吡唑-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.237 | CH3 | CH3 | 1-甲氧基吡唑-5-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.238 | CH3 | CH3 | 1-甲氧基吡唑-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.239 | CH3 | CH3 | 1-甲基咪唑-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.240 | CH3 | CH3 | 咪唑-1-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.24l | CH3 | CH3 | [1,2,4]-三唑-1-基 | CH3 | H | Cl | 2 | 顺式 |
No. | R1 | R2 | R3 | R4 | R7 | X | n | 异构体 | 物理数据 |
Ⅰ.242 | CH3 | CH3 | 1-甲基-[1,2,4]-三唑-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.243 | CH3 | CH3 | 2-噻吩基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.244 | CH3 | CH3 | 3-噻吩基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.245 | CH3 | CH3 | 四氢噻喃-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.246 | CH3 | CH3 | 四氢噻喃-4-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.247 | CH3 | CH3 | [1,3]二硫戊环-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.248 | CH3 | CH3 | 2-呋喃基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.249 | CH3 | CH3 | 3-呋喃基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.250 | CH3 | CH3 | 四氢呋喃-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.251 | CH3 | CH3 | 四氢呋喃-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.252 | CH3 | CH3 | [1,3]-二氧戊环-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.253 | CH3 | CH3 | 四氢吡喃-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.254 | CH3 | CH3 | 四氢吡喃-4-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.255 | CH3 | CH3 | [1,3]二噁烷-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.256 | CH3 | CH3 | [1,3,4]-噁二唑-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.257 | CH3 | CH3 | 哌啶-1-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.258 | CH3 | CH3 | 2-吡啶基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.259 | CH3 | CH3 | 6-甲氧基-2-吡啶基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.260 | CH3 | CH3 | 5-三氟甲基-2-吡啶基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.261 | CH3 | CH3 | 2-氯-5-三氟甲基-2-吡啶基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.262 | CH3 | CH3 | 3-吡啶基 | CH3 | H | Cl | 2 | 顺式 |
No. | R1 | R2 | R3 | R4 | R7 | X | n | 异构体 | 物理数据 |
Ⅰ.263 | CH3 | CH3 | 4-吡啶基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.264 | CH3 | CH3 | 吗啉-4-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.265 | CH3 | CH3 | 嘧啶-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.266 | CH3 | CH3 | 嘧啶-4-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.267 | CH3 | CH3 | 吡嗪-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.268 | CH3 | CH3 | 哒嗪-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.269 | CH3 | CH3 | 哒嗪-4-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.270 | CH3 | CH3 | 6-甲基哒嗪-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.271 | CH3 | CH3 | 6-甲氧基哒嗪-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.272 | CH3 | CH3 | [1,3,5]-三嗪-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.273 | CH3 | CH3 | [1,2,4]-三嗪-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.274 | CH3 | CH3 | 苯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.275 | CH3 | CH3 | 2-氟苯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.276 | CH3 | CH3 | 3-三氟甲基苯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.277 | CH3 | CH3 | 2-甲基苯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.278 | CH3 | CH3 | 3-甲基苯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.279 | CH3 | CH3 | 4-甲基苯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.280 | CH3 | CH3 | 4-氯苯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.281 | CH3 | CH3 | 2-氯苯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.282 | CH3 | CH3 | 3-氯苯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.283 | CH3 | CH3 | 4-甲氧基苯基 | CH3 | H | Cl | 2 | 顺式 |
No. | R1 | R2 | R3 | R4 | R7 | X | n | 异构体 | 物理数据 |
Ⅰ.284 | CH3 | CH3 | 甲硫基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.285 | CH3 | CH3 | 甲氧基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.286 | CH3 | CH3 | 乙氧基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.287 | CH3 | CH3 | 2-甲氧基乙氧基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.288 | CH3 | CH3 | 甲酰基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.289 | CH3 | CH3 | 乙酰基氨基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.290 | CH3 | CH3 | 甲基羰基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.291 | CH3 | CH3 | 甲氧基羰基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.292 | CH3 | CH3 | 二甲基氨基羰基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.293 | CH3 | CH3 | 甲氧基亚氨基甲基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.294 | CH3 | CH3 | 乙氧基亚氨基甲基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.295 | CH3 | CH3 | 1-乙氧基亚氨基乙基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.296 | CH3 | CH3 | 1-甲氧基亚氨基乙基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.297 | CH3 | CH3 | 1-乙氧基亚氨基丙基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.298 | CH3 | CH3 | 1-甲氧基亚氨基丙基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.299 | CH3 | CH3 | 氰基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.300 | C2H5 | CH3 | H | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.30l | C2H5 | CH3 | F | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.302 | C2H5 | CH3 | Cl | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.303 | C2H5 | CH3 | Br | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.304 | C2H5 | CH3 | CH3 | CH3 | H | Cl | 2 | 顺式 |
Nr. | R1 | R2 | R3 | R4 | R7 | X | n | 异构体 | 物理数据 |
Ⅰ.305 | C2H5 | CH3 | CF3 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.306 | C2H5 | CH3 | CHF2 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.307 | C2H5 | CH3 | 乙基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.308 | C2H5 | CH3 | 异丙基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.309 | C2H5 | CH3 | 苄基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.310 | C2H5 | CH3 | 4-氯苯基甲基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.311 | C2H5 | CH3 | 烯丙基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.312 | C2H5 | CH3 | 反式-氯烯丙基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.313 | C2H5 | CH3 | 顺式-氯烯丙基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.314 | C2H5 | CH3 | 顺式-2-氯乙烯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.315 | C2H5 | CH3 | 反式-2-氯乙烯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.316 | C2H5 | CH3 | 2,2-二氯乙烯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.317 | C2H5 | CH3 | 丙炔-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.318 | C2H5 | CH3 | 乙炔基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.319 | C2H5 | CH3 | 4,5-二氢异噁唑-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.320 | C2H5 | CH3 | 异噁唑-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.321 | C2H5 | CH3 | 3-甲基异噁唑-5-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.322 | C2H5 | CH3 | 4-甲基-4,5-二氢异噁唑-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.323 | C2H5 | CH3 | 3-乙基-4,5-二氢异噁唑-4-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.324 | C2H5 | CH3 | 3-乙基-4,5-二氢异噁唑-5-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.325 | C2H5 | CH3 | 5-甲基-4,5-二氢异噁唑-3-基 | CH3 | H | Cl | 2 | 顺式 |
Nr. | R1 | R2 | R3 | R4 | R7 | X | n | 异构体 | 物理数据 |
Ⅰ.326 | C2H5 | CH3 | 4,5-二甲基-4,5-二氢异噁唑-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.327 | C2H5 | CH3 | 噻唑-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.328 | C2H5 | CH3 | 5-甲基噻唑-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.329 | C2H5 | CH3 | 噻唑-4-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.330 | C2H5 | CH3 | 噻唑-5-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.331 | C2H5 | CH3 | 噁唑-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.332 | C2H5 | CH3 | 4,5-二氢噁唑-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.333 | C2H5 | CH3 | 吡咯-1-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.334 | C2H5 | CH3 | 吡唑-1-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.335 | C2H5 | CH3 | 1-甲基吡唑-5-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.336 | C2H5 | CH3 | 1-甲基吡唑-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.337 | C2H5 | CH3 | 1-甲氧基吡唑-5-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.338 | C2H5 | CH3 | 1-甲氧基吡唑-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.339 | C2H5 | CH3 | 1-甲基咪唑-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.340 | C2H5 | CH3 | 咪唑-1-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.341 | C2H5 | CH3 | [1,2,4]-三唑-1-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.342 | C2H5 | CH3 | 1-甲基-[1,2,4]-三唑-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.343 | C2H5 | CH3 | 2-噻吩基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.344 | C2H5 | CH3 | 3-噻吩基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.345 | C2H5 | CH3 | 四氢噻喃-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.346 | C2H5 | CH3 | 四氢噻喃-4-基 | CH3 | H | Cl | 2 | 顺式 |
Nr. | R1 | R2 | R3 | R4 | R7 | X | n | 异构体 | 物理数据 |
Ⅰ.347 | C2H5 | CH3 | [1,3]二硫戊环-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.348 | C2H5 | CH3 | 2-呋喃基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.349 | C2H5 | CH3 | 3-呋喃基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.350 | C2H5 | CH3 | 四氢呋喃-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.351 | C2H5 | CH3 | 四氢呋喃-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.352 | C2H5 | CH3 | [1,3]二氧戊环-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.353 | C2H5 | CH3 | 四氢吡喃-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.354 | C2H5 | CH3 | 四氢吡喃-4-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.355 | C2H5 | CH3 | [1,3]二噁烷-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.356 | C2H5 | CH3 | [1,3,4]-噁二唑-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.357 | C2H5 | CH3 | 哌啶-1-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.358 | C2H5 | CH3 | 2-吡啶基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.359 | C2H5 | CH3 | 6-甲氧基-2-吡啶基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.360 | C2H5 | CH3 | 5-三氟甲基-2-吡啶基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.361 | C2H5 | CH3 | 2-氯-5-三氟甲基-2-吡啶基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.362 | C2H5 | CH3 | 3-吡啶基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.363 | C2H5 | CH3 | 4-吡啶基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.364 | C2H5 | CH3 | 吗啉-4-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.365 | C2H5 | CH3 | 嘧啶-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.366 | C2H5 | CH3 | 嘧啶-4-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.367 | C2H5 | CH3 | 吡嗪-2-基 | CH3 | H | Cl | 2 | 顺式 |
Nr. | R1 | R2 | R3 | R4 | R7 | X | n | 异构体 | 物理数据 |
Ⅰ.368 | C2H5 | CH3 | 哒嗪-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.369 | C2H5 | CH3 | 哒嗪-4-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.370 | C2H5 | CH3 | 6-甲基哒嗪-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.371 | C2H5 | CH3 | 6-甲氧基哒嗪-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.372 | C2H5 | CH3 | [1,3,5]-三嗪-2-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.373 | C2H5 | CH3 | [1,2,4]-三嗪-3-基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.374 | C2H5 | CH3 | 苯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.375 | C2H5 | CH3 | 2-氟苯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.376 | C2H5 | CH3 | 3-三氟甲基苯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.377 | C2H5 | CH3 | 2-甲基苯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.378 | C2H5 | CH3 | 3-甲基苯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.379 | C2H5 | CH3 | 4-甲基苯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.380 | C2H5 | CH3 | 4-氯苯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.381 | C2H5 | CH3 | 2-氯苯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.382 | C2H5 | CH3 | 3-氯苯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.383 | C2H5 | CH3 | 4-甲氧基苯基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.384 | C2H5 | CH3 | 甲硫基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.385 | C2H5 | CH3 | 甲氧基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.386 | C2H5 | CH3 | 乙氧基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.387 | C2H5 | CH3 | 2-甲氧基乙氧基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.388 | C2H5 | CH3 | 甲酰基 | CH3 | H | Cl | 2 | 顺式 |
Nr. | R1 | R2 | R3 | R4 | R7 | X | n | 异构体 | 物理数据 |
Ⅰ.389 | C2H5 | CH3 | 乙酰基氨基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.390 | C2H5 | CH3 | 甲基羰基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.391 | C2H5 | CH3 | 甲氧基羰基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.392 | C2H5 | CH3 | 二甲基氨基羰基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.393 | C2H5 | CH3 | 甲氧基亚氨基甲基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.394 | C2H5 | CH3 | 乙氧基亚氨基甲基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.395 | C2H5 | CH3 | 1-乙氧基亚氨基乙基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.396 | C2H5 | CH3 | 1-甲氧基亚氨基乙基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.397 | C2H5 | CH3 | 1-乙氧基亚氨基丙基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.398 | C2H5 | CH3 | 1-甲氧基亚氨基丙基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.399 | C2H5 | CH3 | 氰基 | CH3 | H | Cl | 2 | 顺式 | |
Ⅰ.400 | CH3 | Cl | H | CF3 | H | Cl | 2 | 顺式 | |
Ⅰ.401 | CH3 | Cl | F | CF3 | H | Cl | 2 | 顺式 | |
Ⅰ.402 | CH3 | Cl | Cl | CF3 | H | Cl | 2 | 顺式 | |
Ⅰ.403 | CH3 | Cl | Br | CF3 | H | Cl | 2 | 顺式 | |
Ⅰ.404 | CH3 | Cl | CH3 | CF3 | H | Cl | 2 | 顺式 | |
Ⅰ.405 | CH3 | Cl | CF3 | CF3 | H | Cl | 2 | 顺式 | |
Ⅰ.406 | CH3 | Cl | 乙基 | CF3 | H | Cl | 2 | 顺式 | |
Ⅰ.407 | CH3 | Cl | 反式-氯烯丙基 | CF3 | H | Cl | 2 | 顺式 | |
Ⅰ.408 | CH3 | Cl | 2,2-二氯乙烯基 | CF3 | H | Cl | 2 | 顺式 | |
Ⅰ.409 | CH3 | Cl | 4,5-二氢异噁唑-3-基 | CF3 | H | Cl | 2 | 顺式 |
Nr. | R1 | R2 | R3 | R4 | R7 | X | n | 异构物 | 物理数据 |
Ⅰ.410 | CH3 | Cl | 异噁唑-3-基 | CF3 | H | Cl | 2 | 顺式 | |
Ⅰ.411 | CH3 | Cl | 3-甲基异噁唑-5-基 | CF3 | H | Cl | 2 | 顺式 | |
Ⅰ.412 | CH3 | Cl | 4-甲基-4,5-二氢异噁唑-3-基 | CF3 | H | Cl | 2 | 顺式 | |
Ⅰ.413 | CH3 | Cl | 5-甲基-4,5-二氢异噁唑-3-基 | CF3 | H | Cl | 2 | 顺式 | |
Ⅰ.414 | CH3 | Cl | 噻唑-2-基 | CF3 | H | Cl | 2 | 顺式 | |
Ⅰ.415 | CH3 | Cl | 噁唑-2-基 | CF3 | H | Cl | 2 | 顺式 | |
Ⅰ.416 | CH3 | Cl | 4,5-二氢噁唑-2-基 | CF3 | H | Cl | 2 | 顺式 | |
Ⅰ.417 | CH3 | Cl | 1-甲基吡唑-3-基 | CF3 | H | Cl | 2 | 顺式 | |
Ⅰ.418 | CH3 | Cl | 2-噻吩基 | CF3 | H | Cl | 2 | 顺式 | |
Ⅰ.419 | CH3 | Cl | 3-噻吩基 | CF3 | H | Cl | 2 | 顺式 | |
Ⅰ.420 | CH3 | Cl | [1,3]二氧戊环-2-基 | CF3 | H | Cl | 2 | 顺式 | |
Ⅰ.421 | CH3 | Cl | 2-吡啶基 | CF3 | H | Cl | 2 | 顺式 | |
Ⅰ.422 | CH3 | Cl | 3-吡啶基 | CF3 | H | Cl | 2 | 顺式 | |
Ⅰ.423 | CH3 | Cl | 4-吡啶基 | CF3 | H | Cl | 2 | 顺式 | |
Ⅰ.424 | CH3 | Cl | 嘧啶-2-基 | CF3 | H | Cl | 2 | 顺式 | |
Ⅰ.425 | CH3 | Cl | 嘧啶-4-基 | CF3 | H | Cl | 2 | 顺式 | |
Ⅰ.426 | CH3 | Cl | 吡嗪-2-基 | CF3 | H | Cl | 2 | 顺式 | |
Ⅰ.427 | CH3 | Cl | 哒嗪-3-基 | CF3 | H | Cl | 2 | 顺式 | |
Ⅰ.428 | CH3 | Cl | 苯基 | CF3 | H | Cl | 2 | 顺式 | |
Ⅰ.429 | CH3 | Cl | 2-氟苯基 | CF3 | H | Cl | 2 | 顺式 | |
Ⅰ.430 | CH3 | Cl | 3-三氟甲基苯基 | CF3 | H | Cl | 2 | 顺式 |
Nr. | R1 | R2 | R3 | R4 | R7 | X | n | 异构体 | 物理数据 |
Ⅰ.431 | CH3 | Cl | 4-甲基苯基 | CF3 | H | Cl | 2 | 顺式 | |
Ⅰ.432 | CH3 | Cl | 4-氯苯基 | CF3 | H | Cl | 2 | 顺式 | |
Ⅰ.433 | CH3 | Cl | 4-甲氧基苯基 | CF3 | H | Cl | 2 | 顺式 | |
Ⅰ.434 | CH3 | Cl | 甲氧基 | CF3 | H | Cl | 2 | 顺式 | |
Ⅰ.435 | CH3 | Cl | 二甲基氨基羰基 | CF3 | H | Cl | 2 | 顺式 | |
Ⅰ.436 | CH3 | Cl | 甲氧基亚氨基甲基 | CF3 | H | Cl | 2 | 顺式 | |
Ⅰ.437 | CH3 | Cl | H | CH3 | H | Cl | 1 | 顺式 | |
Ⅰ.438 | CH3 | Cl | Cl | CH3 | H | Cl | 1 | 顺式 | |
Ⅰ.439 | CH3 | Cl | CH3 | CH3 | H | Cl | 1 | 顺式 | |
Ⅰ.440 | CH3 | Cl | 4,5-二氢异噁唑-3-基 | CH3 | H | Cl | 1 | 顺式 | |
Ⅰ.441 | CH3 | Cl | 异噁唑-3-基 | CH3 | H | Cl | 1 | 顺式 | |
Ⅰ.442 | CH3 | Cl | 3-甲基异噁唑-5-基 | CH3 | H | Cl | 1 | 顺式 | |
Ⅰ.443 | CH3 | Cl | 噻唑-2-基 | CH3 | H | Cl | 1 | 顺式 | |
Ⅰ.444 | CH3 | Cl | 噁唑-2-基 | CH3 | H | Cl | 1 | 顺式 | |
Ⅰ.445 | CH3 | Cl | 2-吡啶基 | CH3 | H | Cl | 1 | 顺式 | |
Ⅰ.446 | CH3 | Cl | 嘧啶-2-基 | CH3 | H | Cl | 1 | 顺式 | |
Ⅰ.447 | CH3 | Cl | 吡嗪-2-基 | CH3 | H | Cl | 1 | 顺式 | |
Ⅰ.448 | CH3 | Cl | 苯基 | CH3 | H | Cl | 1 | 顺式 | |
Ⅰ.449 | CH3 | Cl | 甲氧基 | CH3 | H | Cl | 1 | 顺式 | |
Ⅰ.450 | CH3 | Cl | H | CH3 | H | Cl | 0 | 顺式 | |
Ⅰ.45l | CH3 | Cl | Cl | CH3 | H | Cl | 0 | 顺式 |
Nr. | R1 | R2 | R3 | R4 | R7 | X | n | 异构体 | 物理数据 |
Ⅰ.452 | CH3 | Cl | CH3 | CH3 | H | Cl | 0 | 顺式 | |
Ⅰ.453 | CH3 | Cl | 4,5-二氢异噁唑-3-基 | CH3 | H | Cl | 0 | 顺式 | |
Ⅰ.454 | CH3 | Cl | 异噁唑-3-基 | CH3 | H | Cl | 0 | 顺式 | |
Ⅰ.455 | CH3 | Cl | 3-甲基异噁唑-5-基 | CH3 | H | Cl | 0 | 顺式 | |
Ⅰ.456 | CH3 | Cl | 噻唑-2-基 | CH3 | H | Cl | 0 | 顺式 | |
Ⅰ.457 | CH3 | Cl | 噁唑-2-基 | CH3 | H | Cl | 0 | 顺式 | |
Ⅰ.458 | CH3 | Cl | 2-吡啶基 | CH3 | H | Cl | 0 | 顺式 | |
Ⅰ.459 | CH3 | Cl | 嘧啶-2-基 | CH3 | H | Cl | 0 | 顺式 | |
Ⅰ.460 | CH3 | Cl | 吡嗪-2-基 | CH3 | H | Cl | 0 | 顺式 | |
Ⅰ.461 | CH3 | Cl | 苯基 | CH3 | H | Cl | 0 | 顺式 | |
Ⅰ.462 | CH3 | Cl | 甲氧基 | CH3 | H | Cl | 0 | 顺式 | |
Ⅰ.463 | CH3 | Cl | H | CH3 | H | Br | 2 | 顺式 | |
Ⅰ.464 | CH3 | Cl | Cl | CH3 | H | Br | 2 | 顺式 | |
Ⅰ.465 | CH3 | Cl | CH3 | CH3 | H | Br | 2 | 顺式 | |
Ⅰ.466 | CH3 | Cl | 4,5-二氢异噁唑-3-基 | CH3 | H | Br | 2 | 顺式 | 参见实施例3 |
Ⅰ.467 | CH3 | Cl | 异噁唑-3-基 | CH3 | H | Br | 2 | 顺式 | |
Ⅰ.468 | CH3 | Cl | 3-甲基异噁唑-5-基 | CH3 | H | Br | 2 | 顺式 | |
Ⅰ.469 | CH3 | Cl | 噻唑-2-基 | CH3 | H | Br | 2 | 顺式 | |
Ⅰ.470 | CH3 | Cl | 噁唑-2-基 | CH3 | H | Br | 2 | 顺式 | |
Ⅰ.471 | CH3 | Cl | 2-吡啶基 | CH3 | H | Br | 2 | 顺式 | |
Ⅰ.472 | CH3 | Cl | 嘧啶-2-基 | CH3 | H | Br | 2 | 顺式 |
Nr. | R1 | R2 | R3 | R4 | R7 | X | n | 异构体 | 物理数据 |
Ⅰ.473 | CH3 | Cl | 吡嗪-2-基 | CH3 | H | Br | 2 | 顺式 | |
Ⅰ.474 | CH3 | Cl | 苯基 | CH3 | H | Br | 2 | 顺式 | |
Ⅰ.475 | CH3 | Cl | 甲氧基 | CH3 | H | Br | 2 | 顺式 | |
Ⅰ.476 | CH3 | Cl | H | CH3 | H | H | 2 | 顺式 | |
Ⅰ.477 | CH3 | Cl | Cl | CH3 | H | H | 2 | 顺式 | |
Ⅰ.478 | CH3 | Cl | CH3 | CH3 | H | H | 2 | 顺式 | |
Ⅰ.479 | CH3 | Cl | 4,5-二氢异噁唑-3-基 | CH3 | H | H | 2 | 顺式 | |
Ⅰ.480 | CH3 | Cl | 异噁唑-3-基 | CH3 | H | H | 2 | 顺式 | |
Ⅰ.481 | CH3 | Cl | 3-甲基异噁唑-5-基 | CH3 | H | H | 2 | 顺式 | |
Ⅰ.482 | CH3 | Cl | 噻唑-2-基 | CH3 | H | H | 2 | 顺式 | |
Ⅰ.483 | CH3 | Cl | 噁唑-2-基 | CH3 | H | H | 2 | 顺式 | |
Ⅰ.484 | CH3 | Cl | 2-吡啶基 | CH3 | H | H | 2 | 顺式 | |
Ⅰ.485 | CH3 | Cl | 嘧啶-2-基 | CH3 | H | H | 2 | 顺式 | |
Ⅰ.486 | CH3 | Cl | 吡嗪-2-基 | CH3 | H | H | 2 | 顺式 | |
Ⅰ.487 | CH3 | Cl | 苯基 | CH3 | H | H | 2 | 顺式 | |
Ⅰ.488 | CH3 | Cl | 甲氧基 | CH3 | H | H | 2 | 顺式 | |
Ⅰ.489 | CH3 | Cl | H | CH3 | H | Cl | 2 | 反式 | |
Ⅰ.490 | CH3 | Cl | Cl | CH3 | H | Cl | 2 | 反式 | |
Ⅰ.491 | CH3 | Cl | CH3 | CH3 | H | Cl | 2 | 反式 | |
Ⅰ.492 | CH3 | Cl | 4,5-二氢异噁唑-3-基 | CH3 | H | Cl | 2 | 反式 | |
Ⅰ.493 | CH3 | Cl | 异噁唑-3-基 | CH3 | H | Cl | 2 | 反式 |
Nr. | R1 | R2 | R3 | R4 | R7 | X | n | 异构体 | 物理数据 |
Ⅰ.494 | CH3 | Cl | 3-甲基异噁唑-5-基 | CH3 | H | Cl | 2 | 反式 | |
Ⅰ.495 | CH3 | Cl | 噻唑-2-基 | CH3 | H | Cl | 2 | 反式 | |
Ⅰ.496 | CH3 | Cl | 噁唑-2-基 | CH3 | H | Cl | 2 | 反式 | |
Ⅰ.497 | CH3 | Cl | 2-吡啶基 | CH3 | H | Cl | 2 | 反式 | |
Ⅰ.498 | CH3 | Cl | 嘧啶-2-基 | CH3 | H | Cl | 2 | 反式 | |
Ⅰ.499 | CH3 | Cl | 吡嗪-2-基 | CH3 | H | Cl | 2 | 反式 | |
Ⅰ.500 | CH3 | Cl | 苯基 | CH3 | H | Cl | 2 | 反式 | |
Ⅰ.501 | CH3 | Cl | 甲氧基 | CH3 | H | Cl | 2 | 反式 | |
Ⅰ.502 | CH3 | Cl | H | CH3 | CH3 | Cl | 2 | 顺式 | |
Ⅰ.503 | CH3 | Cl | Cl | CH3 | CH3 | Cl | 2 | 顺式 | |
Ⅰ.504 | CH3 | Cl | CH3 | CH3 | CH3 | Cl | 2 | 顺式 | |
Ⅰ.505 | CH3 | Cl | 4,5-二氢异噁唑-3-基 | CH3 | CH3 | Cl | 2 | 顺式 | |
Ⅰ.506 | CH3 | Cl | 异噁唑-3-基 | CH3 | CH3 | Cl | 2 | 顺式 | |
Ⅰ.507 | CH3 | Cl | 3-甲基异噁唑-5-基 | CH3 | CH3 | Cl | 2 | 顺式 | |
Ⅰ.508 | CH3 | Cl | 噻唑-2-基 | CH3 | CH3 | Cl | 2 | 顺式 | |
Ⅰ.509 | CH3 | Cl | 噁唑-2-基 | CH3 | CH3 | Cl | 2 | 顺式 | |
Ⅰ.510 | CH3 | Cl | 2-吡啶基 | CH3 | CH3 | Cl | 2 | 顺式 | |
Ⅰ.511 | CH3 | Cl | 嘧啶-2-基 | CH3 | CH3 | Cl | 2 | 顺式 | |
Ⅰ.512 | CH3 | Cl | 吡嗪-2-基 | CH3 | CH3 | Cl | 2 | 顺式 | |
Ⅰ.513 | CH3 | Cl | 苯基 | CH3 | CH3 | Cl | 2 | 顺式 | |
Ⅰ.514 | CH3 | Cl | 甲氧基 | CH3 | CH3 | Cl | 2 | 顺式 |
表2:
Nr. | R1 | R2 | R3 | R4 | R7 | X | n | 物理数据 |
Ⅱ.1 | CH3 | Cl | H | CH3 | H | Br | 2 | |
Ⅱ.2 | CH3 | Cl | Cl | CH3 | H | Br | 2 | |
Ⅱ.3 | CH3 | Cl | CH3 | CH3 | H | Br | 2 | |
Ⅱ.4 | CH3 | Cl | 4,5-二氢异噁唑-3-基 | CH3 | H | Br | 2 | |
Ⅱ.5 | CH3 | Cl | 异噁唑-3-基 | CH3 | H | Br | 2 | |
Ⅱ.6 | CH3 | Cl | 3-甲基异噁唑-5-基 | CH3 | H | Br | 2 | |
Ⅱ.7 | CH3 | Cl | 噻唑-2-基 | CH3 | H | Br | 2 | |
Ⅱ.8 | CH3 | Cl | 噁唑-2-基 | CH3 | H | Br | 2 | |
Ⅱ.9 | CH3 | Cl | 2-吡啶基 | CH3 | H | Br | 2 | |
Ⅱ.10 | CH3 | Cl | 嘧啶-2-基 | CH3 | H | Br | 2 |
Nr. | R1 | R2 | R3 | R4 | R7 | X | n | 物理数据 |
Ⅱ.11 | CH3 | Cl | 吡嗪-2-基 | CH3 | H | Br | 2 | |
Ⅱ.12 | CH3 | Cl | 苯基 | CH3 | H | Br | 2 | |
Ⅱ.13 | CH3 | Cl | 甲氧基 | CH3 | H | Br | 2 | |
Ⅱ.14 | CH3 | Cl | H | CH3 | H | Cl | 2 | |
Ⅱ.15 | CH3 | Cl | Cl | CH3 | H | Cl | 2 | |
Ⅱ.16 | CH3 | Cl | CH3 | CH3 | H | Cl | 2 | |
Ⅱ.17 | CH3 | Cl | 4,5-二氢异噁唑-3-基 | CH3 | H | Cl | 2 | 参见实施例1 |
Ⅱ.18 | CH3 | Cl | 异噁唑-3-基 | CH3 | H | Cl | 2 | |
Ⅱ.19 | CH3 | Cl | 3-甲基异噁唑-5-基 | CH3 | H | Cl | 2 | |
Ⅱ.20 | CH3 | Cl | 噻唑-2-基 | CH3 | H | Cl | 2 | 1H-NMR(270MHz,CDCl3);8,18(d,1H);7,99(d,1H);7,78(d,1H);7,62(m,2H);3,22(s,3H);1,62(s,3H) |
Ⅱ.21 | CH3 | Cl | 噁唑-2-基 | CH3 | H | Cl | 2 | |
Ⅱ.22 | CH3 | Cl | 2-吡啶基 | CH3 | H | Cl | 2 | |
Ⅱ.23 | CH3 | Cl | 嘧啶-2-基 | CH3 | H | Cl | 2 | |
Ⅱ.24 | CH3 | Cl | 吡嗪-2-基 | CH3 | H | Cl | 2 | |
Ⅱ.25 | CH3 | Cl | 苯基 | CH3 | H | Cl | 2 | |
Ⅱ.26 | CH3 | Cl | 甲氧基 | CH3 | H | Cl | 2 |
Nr. | R1 | R2 | R3 | R4 | R7 | X | n | 物理数据 |
Ⅱ.27 | CH3 | CH3 | H | CH3 | H | Cl | 2 | |
Ⅱ.28 | CH3 | CH3 | Cl | CH3 | H | Cl | 2 | |
Ⅱ.29 | CH3 | CH3 | CH3 | CH3 | H | Cl | 2 | |
Ⅱ.30 | CH3 | CH3 | 4,5-二氢异噁唑-3-基 | CH3 | H | Cl | 2 | |
Ⅱ.31 | CH3 | CH3 | 异噁唑-3-基 | CH3 | H | Cl | 2 | |
Ⅱ.32 | CH3 | CH3 | 3-甲基异噁唑-5-基 | CH3 | H | Cl | 2 | |
Ⅱ.33 | CH3 | CH3 | 噻唑-2-基 | CH3 | H | Cl | 2 | |
Ⅱ.34 | CH3 | CH3 | 噁唑-2-基 | CH3 | H | Cl | 2 | |
Ⅱ.35 | CH3 | CH3 | 2-吡啶基 | CH3 | H | Cl | 2 | |
Ⅱ.36 | CH3 | CH3 | 嘧啶-2-基 | CH3 | H | Cl | 2 | |
Ⅱ.37 | CH3 | CH3 | 吡嗪-2-基 | CH3 | H | Cl | 2 | |
Ⅱ.38 | CH3 | CH3 | 苯基 | CH3 | H | Cl | 2 | |
Ⅱ.39 | CH3 | CH3 | 甲氧基 | CH3 | H | Cl | 2 | |
Ⅱ.40 | CH3CH2 | Cl | H | CH3 | H | Br | 2 | |
Ⅱ.41 | CH3CH2 | Cl | Cl | CH3 | H | Br | 2 | |
Ⅱ.42 | CH3CH2 | Cl | CH3 | CH3 | H | Br | 2 | |
Ⅱ.43 | CH3CH2 | Cl | 4,5-二氢异噁唑-3-基 | CH3 | H | Br | 2 | |
Ⅱ.44 | CH3CH2 | Cl | 异噁唑-3-基 | CH3 | H | Br | 2 | |
Ⅱ.45 | CH3CH2 | Cl | 3-甲基异噁唑-5-基 | CH3 | H | Br | 2 | |
Ⅱ.46 | CH3CH2 | Cl | 噻唑-2-基 | CH3 | H | Br | 2 | |
Ⅱ.47 | CH3CH2 | Cl | 噁唑-2-基 | CH3 | H | Br | 2 |
Nr. | R1 | R2 | R3 | R4 | R7 | X | n | 物理数据 |
Ⅱ.48 | CH3CH2 | Cl | 2-吡啶基 | CH3 | H | Br | 2 | |
Ⅱ.49 | CH3CH2 | Cl | 嘧啶-2-基 | CH3 | H | Br | 2 | |
Ⅱ.50 | CH3CH2 | Cl | 吡嗪-2-基 | CH3 | H | Br | 2 | |
Ⅱ.51 | CH3CH2 | Cl | 苯基 | CH3 | H | Br | 2 | |
Ⅱ.52 | CH3CH2 | Cl | 甲氧基 | CH3 | H | Br | 2 | |
Ⅱ.53 | CH3CH2 | Cl | H | CH3 | H | Cl | 2 | |
Ⅱ.54 | CH3CH2 | Cl | Cl | CH3 | H | Cl | 2 | |
Ⅱ.55 | CH3CH2 | Cl | CH3 | CH3 | H | Cl | 2 | |
Ⅱ.56 | CH3CH2 | Cl | 4,5-二氢异噁唑-3-基 | CH3 | H | Cl | 2 | |
Ⅱ.57 | CH3CH2 | Cl | 异噁唑-3-基 | CH3 | H | Cl | 2 | |
Ⅱ.58 | CH3CH2 | Cl | 3-甲基异噁唑-5-基 | CH3 | H | Cl | 2 | |
Ⅱ.59 | CH3CH2 | Cl | 噻唑-2-基 | CH3 | H | Cl | 2 | 1H-NMR(270MHz,CDCl3);8,28(d,1H);7,99(d,1H);7,75(s,1H);7,68(d,1H);4,28(q,2H);3,29(s,3H);1,45(t,3H) |
Ⅱ.60 | CH3CH2 | Cl | 噁唑-2-基 | CH3 | H | Cl | 2 | |
Ⅱ.61 | CH3CH2 | Cl | 2-吡啶基 | CH3 | H | Cl | 2 | |
Ⅱ.62 | CH3CH2 | Cl | 嘧啶-2-基 | CH3 | H | Cl | 2 | |
Ⅱ.63 | CH3CH2 | Cl | 吡嗪-2-基 | CH3 | H | Cl | 2 |
Nr. | R1 | R2 | R3 | R4 | R7 | X | n | 物理数据 |
Ⅱ.64 | CH3CH2 | Cl | 苯基 | CH3 | H | Cl | 2 | |
Ⅱ.65 | CH3CH2 | Cl | 甲氧基 | CH3 | H | Cl | 2 | |
Ⅱ.66 | CH3CH2 | CH3 | H | CH3 | H | Cl | 2 | |
Ⅱ.67 | CH3CH2 | CH3 | Cl | CH3 | H | Cl | 2 | |
Ⅱ.68 | CH3CH2 | CH3 | CH3 | CH3 | H | Cl | 2 | |
Ⅱ.69 | CH3CH2 | CH3 | 4,5-二氢异噁唑-3-基 | CH3 | H | Cl | 2 | |
Ⅱ.70 | CH3CH2 | CH3 | 异噁唑-3-基 | CH3 | H | Cl | 2 | |
Ⅱ.71 | CH3CH2 | CH3 | 3-甲基异噁唑-5-基 | CH3 | H | Cl | 2 | |
Ⅱ.72 | CH3CH2 | CH3 | 噻唑-2-基 | CH3 | H | Cl | 2 | |
Ⅱ.73 | CH3CH2 | CH3 | 噁唑-2-基 | CH3 | H | Cl | 2 | |
Ⅱ.74 | CH3CH2 | CH3 | 2-吡啶基 | CH3 | H | Cl | 2 | |
Ⅱ.75 | CH3CH2 | CH3 | 嘧啶-2-基 | CH3 | H | Cl | 2 | |
Ⅱ.76 | CH3CH2 | CH3 | 吡嗪-2-基 | CH3 | H | Cl | 2 | |
Ⅱ.77 | CH3CH2 | CH3 | 苯基 | CH3 | H | Cl | 2 | |
Ⅱ.78 | CH3CH2 | CH3 | 甲氧基 | CH3 | H | Cl | 2 |
化合物Ⅰ及其农业上有用的盐适合作为除草剂,它们可以是异构体混合物的形式和纯异构体的形式。包含式Ⅰ化合物的除草组合物在控制非耕作区的植物方面非常有效,特别是在高施用量的情况下尤为如此。它们可以在作物如小麦、稻、玉米、大豆和棉花中防治阔叶杂草和禾本科杂草,而不对作物造成明显的伤害。这种效果特别是出现在低施用量的情况下。
取决于所涉及的施用方法,化合物Ⅰ或含有它的除草组合物也可以用于许多其它作物,用于消灭杂草。适合的是例如下列作物:
洋葱、凤梨、花生、芦笋、甜菜(Beta vulgaris spec.altissima)、芜菁甜菜(Beta vulgaris spec.rapa)、Brassicanapus var.napus、Brassica napus var.napobrassica、蔓菁(Brassica rapa var.silvestris)、茶、红花、美洲山核桃、柠檬、甜橙、小果咖啡(中果咖啡、大果咖啡)、黄瓜、狗牙根、胡萝卜、油棕、欧洲草莓、大豆、陆地棉、(鸡脚棉、草棉、Gossypiumvitifolium)、向日葵、巴西橡胶、大麦、啤酒花、甘蓝、核桃、兵豆、亚麻、蕃茄、苹果属、木薯、紫花苜蓿、芭蕉属、烟草(黄花烟草),油橄榄、稻、雪豆、菜豆、欧洲云杉、松属、豌豆、欧洲甜樱桃、桃、西洋梨、红醋栗、蓖麻、甘蔗、黑麦、马铃薯、芦黍(蜀黍)、可可、红车轴草、普通小麦、硬粒小麦、蚕豆、葡萄、玉米。
此外,化合物Ⅰ也可以应用在这样的作物上,所述作物通过育种,包括基因工程的方法,业已对除草剂的作用具有耐受性。
除草组合物或活性成分的施用可在苗前或苗后进行,如果活性成分对某些作物来说是较不耐受的,则应采用这样的施用技术,其中借助于喷雾装置喷雾除草组合物,使其尽可能不触及敏感作物的叶面,同时活性成分到达生长于其下的不希望有的植物的叶面或未覆盖的土壤表面上(苗后铺施(post-directed,lay-by)。
化合物Ⅰ和含有它的除草组合物例如可以以可直接喷雾水溶液、粉末、悬浮液、高浓度的水性、油性或其他悬浮液或分散液、乳液、油分散液、膏剂、喷粉组合物、撒施组合物或颗粒的形式通过喷雾、弥雾、喷粉、撒施或浇注使用。使用形式取决于应用目的,在任何情况下应该保证本发明的活性物质尽可能细的分散。
适合的惰性辅助剂主要是:中等至高沸点的石油馏分如煤油和柴油,煤焦油以及来源于植物和动物的油类,脂族、环状和芳族烃例如石蜡、四氢化萘、烷基化的萘和其衍生物,烷基化的苯和其衍生物,醇类如甲醇、乙醇、丙醇、丁醇和环己醇,酮如环己酮,强极性溶剂例如胺如N-甲基吡咯烷酮和水。
含水的使用形式可由乳油、悬浮液、膏剂、可湿性粉剂或可以用水分散的颗粒通过添加水而制备的。为了制备乳液、膏剂或油分散液,亚苄基吡唑啉酮本身或其溶解在油或溶剂中,借助于润湿剂、粘附剂、分散剂或乳化剂在水中均化。然而同样可以制备由活性物质、润湿剂、粘附剂、分散剂或乳化剂和可能的话溶剂或油组成的适合于用水稀释的浓缩物。
适合的表面活性物质是芳族磺酸例如木质素磺酸、苯酚磺酸、萘磺酸和二丁基萘磺酸以及脂肪酸的碱金属盐、碱土金属盐、铵盐,烷基磺酸和烷芳基磺酸、烷基硫酸、十二烷基醚硫酸和脂肪醇硫酸的碱金属盐、碱土金属盐和铵盐,以及硫酸化的十六烷基醇、十七烷基醇和十八烷基醇以及脂肪醇乙二醇醚的盐,磺化的萘和其衍生物与甲醛的缩合产物,萘或萘磺酸与苯酚和甲醛的缩合产物,聚氧乙烯辛基苯酚醚,乙氧基化异辛基-、辛基-或壬基苯酚,烷基苯基-、三丁基苯基聚乙二醇醚,烷芳基聚醚醇,异十三烷基醇、脂肪醇氧化乙烯缩合物,乙氧基化蓖麻油,聚氧乙烯烷基醚或聚氧丙烯烷基醚,十二烷基醇聚乙二醇醚乙酸酯,山梨醇酯、木素亚硫酸盐废液或甲基纤维素。
粉剂、撒施用材料和喷粉剂可以通过活性物质与固态载体的混合或混磨来制备。
颗粒剂例如包衣、浸渍和匀质颗粒可以通过将活性物质粘合在固态载体上来制备。固态载体是矿质土类如硅酸、硅胶、硅酸盐、滑石、高岭土、石灰石、石灰、白垩、红玄武土、黄土、陶土、白云石、硅藻土、硫酸钙和硫酸镁、氧化镁、磨细的塑料、肥料,如硫酸铵、磷酸铵、硝酸铵、尿素和植物产品如谷类作物粉末、树皮、木材和坚果壳粉,纤维素粉末或其他固态载体。
活性化合物Ⅰ在可直接使用的制剂中的浓度可以在较宽的范围内变化。一般所使用的制剂包含约按重量计0.001至98%、优选按重量计0.01至95%的至少一种活性物质。活性物质的纯度是90%至100%,优选95%至100%(根据NMR-光谱)。
本发明的化合物Ⅰ例如可如下配制成制剂:
Ⅰ、将20重量份的序号Ⅰ.20化合物溶解在一种混合物中,该混合物由80重量份的烷基化苯、10重量份的8~10摩尔氧化乙烯在1摩尔油酸-N-单乙醇酰胺上的加成产物、5重量份的十二烷基苯磺酸的钙盐和5重量份的40摩尔氧化乙烯在1摩尔蓖麻油上的加成产物组成。通过将溶液倾入100000重量份的水中并细分散得到一种水分散液,其包含0.02重量%的活性物质。
Ⅱ、将20重量份的序号Ⅰ.119化合物溶解在一种混合物中,该混合物由40重量份的环己酮、30重量份的异丁醇、20重量份7摩尔氧化乙烯在1摩尔异辛基苯酚上的加成产物和10重量份的40摩尔氧化乙烯在1摩尔蓖麻油上的加成产物组成。通过将溶液倾入100000重量份的水中并细分散得到一种水分散液,其包含0.02重量%的活性物质。
Ⅲ、将20重量份的序号Ⅰ.466活性化合物溶解在一种混合物中,该混合物由25重量份的环己酮、65重量份的沸点为210~280℃的石油馏分和10重量份的40摩尔氧化乙烯在1摩尔蓖麻油上的加成产物组成。通过将该溶液倾入100000重量份的水中并细分散得到一种水分散液,其包含0.02重量%的活性物质。
Ⅳ、将20重量份的序号Ⅰ.20活性化合物与3重量份的二异丁基萘磺酸的钠盐、17重量份来自亚硫酸盐废液的木素磺酸的钠盐和60重量份的粉状硅胶均匀地混合,并在锤磨机中粉磨。通过该混合物在20000重量份水中的均匀分散得到一种喷雾混合物,其包含0.1重量%的活性物质。
Ⅴ、将3重量份的序号Ⅰ.119活性化合物与97重量分的细高岭土混合。按照这种方式得到一种喷粉组合物,其包含3重量%的活性物质。
Ⅵ、将20重量份的序号Ⅰ.466活性成分与2重量份的十二烷基苯磺酸钙、8重量份的脂肪醇-聚乙二醇醚、2重量份的苯酚-尿素-甲醛缩合物的钠盐和68重量份的石蜡样的矿物油均匀地混合。得到一种稳定的油分散液。
Ⅶ、将1重量份的序号Ⅰ.20的活性成分溶解在一种混合物中,该混合物由70重量份的环己酮、20重量份的乙氧基化的异辛基苯酚和10重量份的乙氧基化的蓖麻油组成。得到一种稳定的乳油。
Ⅷ、将1重量份的序号Ⅰ.119的活性物质溶解在一种混合物中,该混合物由80重量份的环己酮和20重量份的Wettol_EM 31(基于乙氧基化蓖麻油的非离子乳化剂)组成。得到一种稳定的乳油。
为了扩展作用谱和得到协同的效果,亚苄基吡唑啉酮可以与众多的具有代表性的其他除草剂或生长调节活性物质混合和一起使用。例如可以作为混合组分的是1,2,4-噻二唑类、1,3,4-噻二唑类,酰胺类、氨基磷酸类和其衍生物,氨基三唑类,N-酰苯胺类、(杂)芳氧基链烷酸类和其衍生物、苯甲酸和其衍生物、苯并噻二嗪酮类、2-芳酰基-1,3-环己二酮类、杂芳基-芳基-酮类、苄基异噁唑烷酮类、间-CF3-苯基衍生物、氨基甲酸酯类、喹啉羧酸和其衍生物、氯乙酰苯胺类、环己-1,3-二酮衍生物、二嗪类、二氯丙酸和其衍生物、二氢苯并呋喃类、二氢呋喃-3-酮类、二硝基苯胺类、二硝基苯酚类、二苯基醚类、联吡啶类(Dipyridyle)、卤代羧酸和其衍生物、脲类、3-苯基尿嘧啶类、咪唑类、咪唑啉酮类、N-苯基-3,4,5,6-四氢邻苯二甲酰亚胺类、噁二唑类、环氧乙烷类、苯酚类、芳氧基-和杂芳氧基苯氧基丙酸酯类、苯乙酸和其衍生物、苯丙酸和其衍生物、吡唑类、苯基吡唑类、哒嗪类、吡啶羧酸和其衍生物、嘧啶基醚类、磺酰胺类、磺酰脲类、三嗪类、三嗪酮类、三唑啉酮类、三唑甲酰胺类和尿嘧啶类。
此外,有利的是化合物Ⅰ单独或与其他的除草剂一起与其他的作物保护剂混合使用,例如与防治害虫或植物病原真菌或细菌的药剂一起使用。此外,感兴趣的是与无机盐溶液的可混合性,采用这种方法来消除营养和微量元素的缺乏。同样可以加入无植物毒性的油和油浓缩物。
根据防治对象、季节、靶体植物和生长阶段的不同,活性化合物的施用剂量是0.001至3.0,优选0.01至1.0kg/ha活性物质(a.s.)。
应用实施例
式Ⅰ的亚苄基吡唑啉酮除草活性通过下述温室试验说明:
所用的栽培容器是塑料花盆,盆中装有腐殖质含量约为3.0%的壤砂土作为基质。根据不同的种类,分别播种不同试验植物的种子。
在苗前处理的情况下,在播种后,就将悬浮或乳化于水中的活性化合物通过细分布的喷嘴施用。向花盆适当浇些水,以促使萌发和生长,然后,覆盖上透明塑料地膜,直到植物生根。如果不是受活性化合物不利影响的话,覆盖应会使试验植物均匀地萌发。
进行苗后处理时,先让试验植物长出,根据不同的生长形式,让其长到3至15cm高,此时方用悬浮或乳化于水中的活性化合物处理。为此,试验植物或是直接播种并在相同花盆中生长,或是先作为秧苗分别生长,再在处理前几天,将它们移栽到试验花盆中。苗后处理的施用量是0.125或0.0625kg/ha a.s.(活性物质)。
根据种类的不同,将植物放置在10-25℃或20-35℃温度下。试验期历经2至4周。在此期间,悉心照料植物,并评价它们对各处理的反应。
以0至100的等级进行评分。在此情况下,100是指没有植物出苗或至少完全毁灭地上部分,而0是指无伤害或生长正常。
在温室试验的苗后方法中使用的植物是由下列品种组成的:
学名 | 俗名 |
有害植物 | |
Chenopodium album | 红心藜 |
Echinochloa crus-galli | 稗草 |
Polygonum persicaria | 春蓼 |
Setaria faberii | 大狗尾草 |
有用植物 | |
Zea mays | 玉米 |
结果显示,用化合物Ⅰ.119处理能非常有效地防治上述有害植物(>98%损害率),而对有用植物玉米却不造成可察觉到的损害(0%损害率)。
表A中的给出的比较实验表明,与由JP-A 61268670(CA,106:209479)已知的化合物A相比,根据本发明的化合物Ⅰ.119具有改进的除草作用。
表A苗后温室实验
实施例序号 | Ⅰ.119 | A | |||
R1 | 4,5-二氢异噁唑-3-基 | H | |||
R2 | SO2CH3 | Cl | |||
施用剂量(g/ha a.s.) | 0.5 | 0.25 | 0.5 | 0.25 | |
试验植物(损害%) | |||||
反枝苋 | 100 | 100 | 40 | 30 | |
稗草 | 100 | 100 | 80 | 70 | |
大狗尾草 | 100 | 100 | 10 | 10 | |
龙葵 | 100 | 100 | 70 | 50 |
Claims (10)
1.式Ⅰ的亚苄基吡唑啉酮:
其中取代基和符号n具有下列含意:
R1是未取代或取代的C1-C6-烷基;
R2是未取代或取代的C1-C6-烷基、未取代或取代的C1-C6-烷氧基、卤素、硝基、氰基;
R3是氢、卤素、硝基、氰基、基团NR5R6、OCOR5、NR5COR6、CO2R5、-COSR5、-CONR6R6、C1-C4-烷氧基亚氨基烷基、C1-C6-烷基羰基、未取代或取代的C1-C6-烷基、未取代或取代的C1-C6-烷氧基、未取代或取代的C1-C6-烷硫基、未取代或取代的C2-C6-烯基、未取代或取代的C2-C6-炔基、未取代或取代的苯基、未取代或取代的苯氧基、可以含有至多4个氮原子和/或至多2个氧原子或硫原子作为环成员的未取代或取代的5-或6-元饱和或不饱和杂环;
R4是C1-C6-烷基、C1-C4-卤代烷基;或
R3和R4形成任选取代的饱和或不饱和2-或3-元桥,该桥可以含有一可以被氧化成亚砜或砜的硫原子;
R5是氢或未取代或取代的C1-C6-烷基;
R6是未取代或取代的C1-C6-烷基;
R7是氢、C1-C6-烷基或C1-C4-卤代烷基;
n是O、1或2;
X是氢、氯或溴;
其中所要求保护的这些化合物可以以反式或顺式形式或这些异构体的混合物的形式存在。
2.权利要求1的式Ⅰ亚苄基吡唑啉酮,其中取代基具有下列含意:
R1是C1-C4-烷基或C1-C4-卤代烷基;
R2是C1-C4-烷基、C1-C4-卤代烷基、C1-C4-烷氧基、C1-C4-卤代烷氧基、卤素、硝基、氰基;
R3是氢、卤素、硝基、氰基、基团NR5R6、OCOR5、NR5COR6、CO2R5、-COSR5、-CONR5R6、C1-C4-烷氧基亚氨基烷基、C1-C4-烷基羰基;下列基团是未取代的或由卤素、C1-C4-烷氧基或苯基取代,其中,苯环可以带有一至五个选自卤素、C1-C2-烷基或C1-C2-烷氧基的取代基:C1-C4-烷基、C1-C4-烷氧基、C1-C4-烷硫基、C2-C6-烯基、C2-C6-炔基;下列基团是未取代的或由C1-C4-烷基、C1-C4-烷氧基、C1-C4-卤代烷基、C1-C4-卤代烷氧基、卤素、苯基、氰基、C1-C4-烷氧羰基或硝基取代:苯基、苯氧基、5-或6-元饱和或不饱和杂环,该杂环可以含有至多4个氮原子和/或至多2个氧或硫原子作为环成员;
R5是氢、C1-C4-烷基,该烷基是未取代的或由卤素、C1-C4-烷氧基或苯基取代,其中苯环可以带有一至五个选自卤素、C1-C2-烷基和C1-C2-烷氧基的取代基;
R6是C1-C4-烷基,该烷基是未取代的或由卤素、C1-C4-烷氧基或苯基取代,其中苯环可以带有一至五个选自卤素、C1-C2-烷基和C1-C2-烷氧基的取代基。
3.权利要求2的式Ⅰ亚苄基吡唑啉酮,其中X是氯。
4.权利要求2的式Ⅰ亚苄基吡唑啉酮,其中R7是氢。
5.权利要求2的式Ⅰ亚苄基吡唑啉酮,其中
R2是C1-C4-烷基、C1-C4-卤代烷基、C1-C4-烷氧基、C1-C4-卤代烷氧基或卤素;
R3是未取代或由C1-C4-烷基、C1-C4-烷氧基、C1-C4-卤代烷基、C1-C4-卤代烷氧基或卤素取代的选自下列的5-或6-元饱和或不饱和杂环:四氢呋喃基、四氢噻吩基、吡咯烷基、异噁唑烷基、异噻唑烷基、吡唑烷基、唑烷基、噻唑烷基、咪唑烷基、1,2,4-噁二唑烷基、1,2,4-噻二唑烷基、1,2,4-三唑烷基、1,3,4-噁二唑烷基、1,3,4-噻二唑烷基、1,3,4-三唑烷基、2,3-二氢呋喃基、2,5-二氢呋喃基、2,3-二氢噻吩基、2,5-二氢噻吩基、2,3-二氢吡咯基、2,5-二氢吡咯基、2,3-二氢异噁唑基、4,5-二氢异噁唑基、2,5-二氢异噁唑基、2,5-二氢噁唑基、2,3-二氢异噻唑基、4,5-二氢异噻唑基、2,5-二氢异噻唑基、2,3-二氢吡唑基、4,5-二氢吡唑基、2,5-二氢吡唑基、2,3-二氢噁唑基、4,5-二氢噁唑基、2,5-二氢噁唑基、2,3-二氢噻唑基、4,5-二氢噻唑基、2,5-二氢噻唑基、2,3-二氢咪唑基、4,5-二氢咪唑基、2,5-二氢咪唑基、吗啉基、哌啶基、四氢哒嗪基、四氢嘧啶基、四氢吡嗪基、1,3,5-四氢三嗪基、1,2,4-四氢三嗪基、1,3-二氢噁嗪基、1,3-二噻烷基、四氢吡喃基、四氢噻喃基、1,3-二氧戊环基、1,1-二氧代-2,3,4,5-四氢噻吩基、1,3-二氢噁嗪基、呋喃基、噻吩基、吡咯基、异噁唑基、异噻唑基、吡唑基、噁唑基、噻唑基、咪唑基、1,2,4-噁二唑基、1,2,4-噻二唑基、1,2,4-三唑基、四唑基、1,3,4-噁二唑基、1,3,4-噻二唑基、1,3,4-三唑基、吡啶基、哒嗪基、嘧啶基、吡嗪基、1,3,5-三嗪基、1,2,4-三嗪基、1,2,4,5-四嗪基;
R4是C1-C4-烷基;
R5是氢、C1-C4-烷基,该烷基是未取代的或由卤素或C1-C4-烷氧基取代;
R6是C1-C4-烷基,该烷基是未取代的或由卤素或C1-C4-烷氧基取代;
R7是氢;
n是2;
X是氢或氯。
6.一种组合物,它包含除草有效量的至少一种权利要求1的式Ⅰ亚苄基吡唑啉酮和常规用于作物保护剂配制的辅助剂。
7.一种制备权利要求8的除草活性组合物的方法,它包含将除草有效量的至少一种权利要求1的式Ⅰ亚苄基吡唑啉酮与常规用于作物保护剂配制的辅助剂混合。
8.一种防治有害植物的方法,它包含使除草有效量的至少一种权利要求1的式Ⅰ亚苄基吡唑啉酮作用于植物、其栖生地和/或种子。
R1是C1-C4-烷基或C1-C4-卤代烷基;
R2是C1-C4-烷基、C1-C4-卤代烷基、C1-C4-烷氧基、C1-C4-卤代烷氧基或卤素;
R3是未取代或由C1-C4-烷基、C1-C4-烷氧基、C1-C4-卤代烷基、C1-C4-卤代烷氧基或卤素取代的选自下列的5-或6-元饱和或不饱和杂环:四氢呋喃基、四氢噻吩基、吡咯烷基、异噁唑烷基、异噻唑烷基、吡唑烷基、噁唑烷基、噻唑烷基、咪唑烷基、1,2,4-噁二唑烷基、1,2,4-噻二唑烷基、1,2,4-三唑烷基、1,3,4-噁二唑烷基、1,3,4-噻二唑烷基、1,3,4-三唑烷基、2,3-二氢呋喃基、2,5-二氢呋喃基、2,3-二氢噻吩基、2,5-二氢噻吩基、2,3-二氢吡咯基、2,5-二氢吡咯基、2,3-二氢异噁唑基、4,5-二氢异噁唑基、2,5-二氢异噁唑基、2,5-二氢噁唑基、2,3-二氢异噻唑基、4,5-二氢异噻唑基、2,5-二氢异噻唑基、2,3-二氢吡唑基、4,5-二氢吡唑基、2,5-二氢吡唑基、2,3-二氢噁唑基、4,5-二氢噁唑基、2,5-二氢噁唑基、2,3-二氢噻唑基、4,5-二氢噻唑基、2,5-二氢噻唑基、2,3-二氢咪唑基、4,5-二氢咪唑基、2,5-二氢咪唑基、吗啉基、哌啶基、四氢哒嗪基、四氢嘧啶基、四氢吡嗪基、1,3,5-四氢三嗪基、1,2,4-四氢三嗪基、1,3-二氢噁嗪基、1,3-二噻烷基、四氢吡喃基、四氢噻喃基、1,3-二氧戊环基、1,1-二氧代-2,3,4,5-四氢噻吩基、1,3-二氢噁嗪基、呋喃基、噻吩基、吡咯基、异噁唑基、异噻唑基、吡唑基、噁唑基、噻唑基、咪唑基、1,2,4-噁二唑基、1,2,4-噻二唑基、1,2,4-三唑基、四唑基、1,3,4-噁二唑基、1,3,4-噻二唑基、1,3,4-三唑基、吡啶基、哒嗪基、嘧啶基、吡嗪基、1,3,5-三嗪基、1,2,4-三嗪基、1,2,4,5-四嗪基;
R4是C1-C4-烷基或C1-C4-卤代烷基;
R7是氢、C1-C4-烷基或C1-C4-卤代烷基;
n是0、1或2;
X是氯或溴。
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19751722 | 1997-11-21 | ||
DE19751722.6 | 1997-11-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
CN1283191A true CN1283191A (zh) | 2001-02-07 |
Family
ID=7849480
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN98812494A Pending CN1283191A (zh) | 1997-11-21 | 1998-11-06 | 亚苄基吡唑啉酮、其制备和应用 |
Country Status (18)
Country | Link |
---|---|
US (2) | US6271179B1 (zh) |
EP (1) | EP1044191A2 (zh) |
JP (1) | JP2001524471A (zh) |
KR (1) | KR20010032321A (zh) |
CN (1) | CN1283191A (zh) |
AR (1) | AR013776A1 (zh) |
AU (1) | AU757752C (zh) |
BG (1) | BG104471A (zh) |
BR (1) | BR9814232A (zh) |
CA (1) | CA2310087A1 (zh) |
EA (1) | EA200000560A1 (zh) |
HU (1) | HUP0100011A3 (zh) |
IL (1) | IL136111A0 (zh) |
NZ (1) | NZ505142A (zh) |
PL (1) | PL341679A1 (zh) |
SK (1) | SK6952000A3 (zh) |
WO (1) | WO1999026930A2 (zh) |
ZA (1) | ZA9810625B (zh) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102408428A (zh) * | 2011-07-26 | 2012-04-11 | 中国农业大学 | 1,2-氮杂环辛烷并吡唑烷酮类化合物及其制备方法与应用 |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
MXPA01008929A (es) * | 1999-03-05 | 2002-04-24 | Basf Ag | Mezcla herbicida que contiene un derivado benzoilo sustituido con 3-heterociclilo y un coadyuvante. |
CN1409710A (zh) | 1999-12-02 | 2003-04-09 | 巴斯福股份公司 | 环丙基稠合的3-(4,5-二氢异噁唑-3-基)-取代的苯甲酰基吡唑 |
CA2393989A1 (en) * | 1999-12-02 | 2001-06-07 | Basf Aktiengesellschaft | 3-(4,5-dihydroisoxazol-3-yl)-substituted benzoylpyrazoles as herbicides |
US6465395B2 (en) | 2000-03-01 | 2002-10-15 | Basf Aktiengesellschaft | Substituted methylene pyrazolinones and the herbicidal use thereof |
WO2006106954A1 (ja) * | 2005-03-31 | 2006-10-12 | Ishihara Sangyo Kaisha, Ltd. | ベンゾイルピラゾール系化合物、それらの製造方法及びそれらを含有する除草剤 |
US20100331315A1 (en) * | 2009-06-18 | 2010-12-30 | Mustapha Haddach | Rhodanines and related heterocycles as kinase inhibitors |
JP2017075161A (ja) * | 2015-11-26 | 2017-04-20 | 住友化学株式会社 | 有害生物防除組成物およびその用途 |
CN108713013B (zh) * | 2016-02-29 | 2021-06-18 | 住友化学株式会社 | 杂环化合物 |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5436648B2 (zh) * | 1974-03-28 | 1979-11-10 | ||
US4382948A (en) * | 1982-03-25 | 1983-05-10 | Chevron Research Company | 1,3,4-Trisubstituted-2-pyrazolin-5-one fungicides |
JPS5955872A (ja) * | 1982-09-22 | 1984-03-31 | Otsuka Chem Co Ltd | 4,4−(α−メチルベンジリデン)−2−ピラゾ−ル−5−オン誘導体 |
JPS61268670A (ja) * | 1985-05-22 | 1986-11-28 | Hodogaya Chem Co Ltd | ピラゾ−ル系化合物およびこれを含有する除草剤 |
IL85659A (en) | 1987-03-17 | 1992-03-29 | Nissan Chemical Ind Ltd | 4-benzoylpyrazole derivatives,method for their preparation and herbicidal compositions containing them |
US4885022A (en) | 1987-03-17 | 1989-12-05 | Nissan Chemical Industries Ltd. | Herbicidal pyrazole derivatives |
GB2224208A (en) * | 1988-10-20 | 1990-05-02 | Shell Int Research | Fungicidal pyrazolyl aryl ketones |
JPH0429129A (ja) * | 1990-05-24 | 1992-01-31 | Konica Corp | ハロゲン化銀写真感光材料 |
JPH04253039A (ja) * | 1991-01-30 | 1992-09-08 | Toshiba Corp | 有機非線形光学材料 |
ATE310739T1 (de) | 1995-02-24 | 2005-12-15 | Pyrazol-4-yl-benzoylderivate und ihre verwendung als herbizide |
-
1998
- 1998-11-06 IL IL13611198A patent/IL136111A0/xx unknown
- 1998-11-06 PL PL98341679A patent/PL341679A1/xx not_active Application Discontinuation
- 1998-11-06 AU AU16670/99A patent/AU757752C/en not_active Ceased
- 1998-11-06 KR KR1020007005533A patent/KR20010032321A/ko not_active Application Discontinuation
- 1998-11-06 EA EA200000560A patent/EA200000560A1/ru unknown
- 1998-11-06 HU HU0100011A patent/HUP0100011A3/hu unknown
- 1998-11-06 CA CA002310087A patent/CA2310087A1/en not_active Abandoned
- 1998-11-06 NZ NZ505142A patent/NZ505142A/xx unknown
- 1998-11-06 WO PCT/EP1998/007099 patent/WO1999026930A2/de not_active Application Discontinuation
- 1998-11-06 JP JP2000522088A patent/JP2001524471A/ja not_active Withdrawn
- 1998-11-06 BR BR9814232-1A patent/BR9814232A/pt not_active IP Right Cessation
- 1998-11-06 EP EP98961147A patent/EP1044191A2/de not_active Withdrawn
- 1998-11-06 CN CN98812494A patent/CN1283191A/zh active Pending
- 1998-11-06 SK SK695-2000A patent/SK6952000A3/sk unknown
- 1998-11-20 ZA ZA9810625A patent/ZA9810625B/xx unknown
- 1998-11-20 AR ARP980105925A patent/AR013776A1/es unknown
- 1998-11-21 US US09/554,184 patent/US6271179B1/en not_active Expired - Fee Related
-
2000
- 2000-05-23 BG BG104471A patent/BG104471A/xx unknown
-
2001
- 2001-01-22 US US09/765,626 patent/US6500950B1/en not_active Expired - Fee Related
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102408428A (zh) * | 2011-07-26 | 2012-04-11 | 中国农业大学 | 1,2-氮杂环辛烷并吡唑烷酮类化合物及其制备方法与应用 |
CN102408428B (zh) * | 2011-07-26 | 2014-01-15 | 中国农业大学 | 1,2-氮杂环辛烷并吡唑烷酮类化合物及其制备方法与应用 |
Also Published As
Publication number | Publication date |
---|---|
AU757752C (en) | 2003-09-11 |
EA200000560A1 (ru) | 2000-12-25 |
SK6952000A3 (en) | 2001-02-12 |
AR013776A1 (es) | 2001-01-10 |
WO1999026930A3 (de) | 1999-08-19 |
JP2001524471A (ja) | 2001-12-04 |
BG104471A (en) | 2001-08-31 |
NZ505142A (en) | 2003-03-28 |
US6500950B1 (en) | 2002-12-31 |
AU757752B2 (en) | 2003-03-06 |
WO1999026930A2 (de) | 1999-06-03 |
HUP0100011A2 (hu) | 2001-05-28 |
IL136111A0 (en) | 2001-05-20 |
EP1044191A2 (de) | 2000-10-18 |
ZA9810625B (en) | 2000-05-22 |
AU1667099A (en) | 1999-06-15 |
CA2310087A1 (en) | 1999-06-03 |
HUP0100011A3 (en) | 2003-03-28 |
US6271179B1 (en) | 2001-08-07 |
BR9814232A (pt) | 2000-10-03 |
KR20010032321A (ko) | 2001-04-16 |
PL341679A1 (en) | 2001-04-23 |
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