CN1169716A - 烷氧基亚氨基乙酰胺 - Google Patents
烷氧基亚氨基乙酰胺 Download PDFInfo
- Publication number
- CN1169716A CN1169716A CN96191663A CN96191663A CN1169716A CN 1169716 A CN1169716 A CN 1169716A CN 96191663 A CN96191663 A CN 96191663A CN 96191663 A CN96191663 A CN 96191663A CN 1169716 A CN1169716 A CN 1169716A
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- ethyl
- methyl
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- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 title abstract description 13
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 23
- 238000000034 method Methods 0.000 claims abstract description 20
- -1 nitro, amino, hydroxyl Chemical group 0.000 claims description 265
- 229910052799 carbon Inorganic materials 0.000 claims description 88
- 150000001875 compounds Chemical class 0.000 claims description 79
- 150000001721 carbon Chemical group 0.000 claims description 75
- 125000000217 alkyl group Chemical group 0.000 claims description 49
- 239000000460 chlorine Substances 0.000 claims description 47
- 229910052801 chlorine Inorganic materials 0.000 claims description 47
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 41
- 239000011737 fluorine Substances 0.000 claims description 41
- 229910052731 fluorine Inorganic materials 0.000 claims description 41
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 41
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 39
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims description 35
- 125000005843 halogen group Chemical group 0.000 claims description 33
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 31
- 229910052736 halogen Inorganic materials 0.000 claims description 30
- 150000002367 halogens Chemical class 0.000 claims description 30
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 28
- 125000003545 alkoxy group Chemical group 0.000 claims description 28
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 28
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 26
- 239000005864 Sulphur Chemical group 0.000 claims description 26
- 125000004414 alkyl thio group Chemical group 0.000 claims description 25
- 229910052760 oxygen Inorganic materials 0.000 claims description 24
- 239000001301 oxygen Substances 0.000 claims description 24
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 23
- 239000001257 hydrogen Substances 0.000 claims description 22
- 229910052739 hydrogen Inorganic materials 0.000 claims description 22
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 21
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 21
- 229910052794 bromium Inorganic materials 0.000 claims description 21
- 125000003118 aryl group Chemical group 0.000 claims description 20
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 20
- 125000001188 haloalkyl group Chemical group 0.000 claims description 20
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 19
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 18
- 125000004432 carbon atom Chemical group C* 0.000 claims description 18
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 18
- 125000003342 alkenyl group Chemical group 0.000 claims description 17
- 125000002541 furyl group Chemical group 0.000 claims description 17
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 16
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 16
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 15
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 claims description 15
- 125000001624 naphthyl group Chemical group 0.000 claims description 15
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 14
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 14
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 14
- CFHIDWOYWUOIHU-UHFFFAOYSA-N oxomethyl Chemical compound O=[CH] CFHIDWOYWUOIHU-UHFFFAOYSA-N 0.000 claims description 14
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 13
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 12
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 12
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 12
- 150000003851 azoles Chemical class 0.000 claims description 12
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 claims description 12
- 125000004429 atom Chemical group 0.000 claims description 11
- 125000001544 thienyl group Chemical group 0.000 claims description 11
- 125000002947 alkylene group Chemical group 0.000 claims description 10
- 150000002431 hydrogen Chemical class 0.000 claims description 10
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 claims description 10
- 125000006216 methylsulfinyl group Chemical group [H]C([H])([H])S(*)=O 0.000 claims description 10
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims description 10
- 125000004076 pyridyl group Chemical group 0.000 claims description 10
- 125000005493 quinolyl group Chemical group 0.000 claims description 10
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 claims description 10
- 125000004205 trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 claims description 10
- 125000003258 trimethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])[*:1] 0.000 claims description 10
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 9
- 150000001412 amines Chemical class 0.000 claims description 9
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 9
- 125000000392 cycloalkenyl group Chemical group 0.000 claims description 9
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 claims description 9
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 9
- WIHIUTUAHOZVLE-UHFFFAOYSA-N 1,3-diethoxypropan-2-ol Chemical compound CCOCC(O)COCC WIHIUTUAHOZVLE-UHFFFAOYSA-N 0.000 claims description 8
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 8
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 8
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 8
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 8
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims description 8
- 125000000031 ethylamino group Chemical group [H]C([H])([H])C([H])([H])N([H])[*] 0.000 claims description 8
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims description 8
- 241000790917 Dioxys <bee> Species 0.000 claims description 7
- 125000002252 acyl group Chemical group 0.000 claims description 7
- 125000003282 alkyl amino group Chemical group 0.000 claims description 7
- 125000004618 benzofuryl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 claims description 7
- 125000004786 difluoromethoxy group Chemical group [H]C(F)(F)O* 0.000 claims description 7
- 125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 7
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 7
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 7
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 6
- 239000005977 Ethylene Substances 0.000 claims description 6
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims description 6
- 125000003302 alkenyloxy group Chemical group 0.000 claims description 6
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims description 6
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 claims description 6
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims description 6
- 125000005278 alkyl sulfonyloxy group Chemical group 0.000 claims description 6
- 125000003368 amide group Chemical group 0.000 claims description 6
- 229910021529 ammonia Inorganic materials 0.000 claims description 6
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 6
- 125000005291 haloalkenyloxy group Chemical group 0.000 claims description 6
- 125000004440 haloalkylsulfinyl group Chemical group 0.000 claims description 6
- 125000001786 isothiazolyl group Chemical group 0.000 claims description 6
- HZVOZRGWRWCICA-UHFFFAOYSA-N methanediyl Chemical group [CH2] HZVOZRGWRWCICA-UHFFFAOYSA-N 0.000 claims description 6
- 125000002757 morpholinyl group Chemical group 0.000 claims description 6
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 claims description 6
- WCPAKWJPBJAGKN-UHFFFAOYSA-N oxadiazole Chemical compound C1=CON=N1 WCPAKWJPBJAGKN-UHFFFAOYSA-N 0.000 claims description 6
- 125000002971 oxazolyl group Chemical group 0.000 claims description 6
- 125000003566 oxetanyl group Chemical group 0.000 claims description 6
- 125000003373 pyrazinyl group Chemical group 0.000 claims description 6
- 125000002098 pyridazinyl group Chemical group 0.000 claims description 6
- 125000001113 thiadiazolyl group Chemical group 0.000 claims description 6
- 125000000335 thiazolyl group Chemical group 0.000 claims description 6
- 239000013543 active substance Substances 0.000 claims description 5
- 150000001335 aliphatic alkanes Chemical class 0.000 claims description 5
- 125000000304 alkynyl group Chemical group 0.000 claims description 5
- 125000004171 alkoxy aryl group Chemical group 0.000 claims description 4
- 125000001118 alkylidene group Chemical group 0.000 claims description 4
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 4
- 125000005110 aryl thio group Chemical group 0.000 claims description 4
- 125000004104 aryloxy group Chemical group 0.000 claims description 4
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims description 4
- 125000006125 ethylsulfonyl group Chemical group 0.000 claims description 4
- 125000004005 formimidoyl group Chemical group [H]\N=C(/[H])* 0.000 claims description 4
- 125000005844 heterocyclyloxy group Chemical group 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- 125000005936 piperidyl group Chemical group 0.000 claims description 4
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims description 3
- 239000004593 Epoxy Substances 0.000 claims description 3
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims description 3
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 3
- PQIOSYKVBBWRRI-UHFFFAOYSA-N methylphosphonyl difluoride Chemical group CP(F)(F)=O PQIOSYKVBBWRRI-UHFFFAOYSA-N 0.000 claims description 3
- 125000004646 sulfenyl group Chemical group S(*)* 0.000 claims description 3
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 claims description 3
- 229930192474 thiophene Natural products 0.000 claims description 3
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 3
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 claims description 2
- 241000607479 Yersinia pestis Species 0.000 claims description 2
- 150000001350 alkyl halides Chemical class 0.000 claims description 2
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims description 2
- 125000000842 isoxazolyl group Chemical group 0.000 claims description 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical group O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 claims 3
- JSLZUBLGGPEVQN-DIPNUNPCSA-N (2r)-4-methyl-2-propan-2-yl-2-[2-[4-[4-[2-(3,4,5-trimethoxyphenyl)ethyl]piperazin-1-yl]butoxy]phenyl]-1,4-benzothiazin-3-one Chemical compound COC1=C(OC)C(OC)=CC(CCN2CCN(CCCCOC=3C(=CC=CC=3)[C@@]3(C(N(C)C4=CC=CC=C4S3)=O)C(C)C)CC2)=C1 JSLZUBLGGPEVQN-DIPNUNPCSA-N 0.000 claims 1
- VOPWNXZWBYDODV-UHFFFAOYSA-N Chlorodifluoromethane Chemical compound FC(F)Cl VOPWNXZWBYDODV-UHFFFAOYSA-N 0.000 claims 1
- 230000002508 compound effect Effects 0.000 claims 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 claims 1
- 229950001891 iprotiazem Drugs 0.000 claims 1
- ZTRPYTHOEREHEN-UHFFFAOYSA-N piperazine pyridine Chemical compound N1CCNCC1.N1=CC=CC=C1.N1=CC=CC=C1 ZTRPYTHOEREHEN-UHFFFAOYSA-N 0.000 claims 1
- 239000002585 base Substances 0.000 description 87
- 125000001309 chloro group Chemical group Cl* 0.000 description 54
- 239000000203 mixture Substances 0.000 description 20
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 18
- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 description 17
- 241000894006 Bacteria Species 0.000 description 16
- 238000005481 NMR spectroscopy Methods 0.000 description 15
- 238000002360 preparation method Methods 0.000 description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
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- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 13
- 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 12
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 12
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- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
- 239000002904 solvent Substances 0.000 description 9
- 150000002148 esters Chemical class 0.000 description 8
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
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- 239000000975 dye Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 239000003995 emulsifying agent Substances 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 5
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
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- 241000233622 Phytophthora infestans Species 0.000 description 5
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 5
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- 239000011574 phosphorus Substances 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
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- 241000233866 Fungi Species 0.000 description 4
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 4
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 4
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 4
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- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 4
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- 125000005842 heteroatom Chemical group 0.000 description 4
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- 229940043265 methyl isobutyl ketone Drugs 0.000 description 4
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- 229910052938 sodium sulfate Inorganic materials 0.000 description 4
- 235000011152 sodium sulphate Nutrition 0.000 description 4
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- QKZMIZCLFDVQJU-UHFFFAOYSA-N [chloro(difluoro)methoxy]-trifluoromethane Chemical compound FC(F)(F)OC(F)(F)Cl QKZMIZCLFDVQJU-UHFFFAOYSA-N 0.000 description 3
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- 125000002877 alkyl aryl group Chemical group 0.000 description 3
- 150000001408 amides Chemical class 0.000 description 3
- 235000013339 cereals Nutrition 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 238000013375 chromatographic separation Methods 0.000 description 3
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- NYPJDWWKZLNGGM-UHFFFAOYSA-N fenvalerate Aalpha Natural products C=1C=C(Cl)C=CC=1C(C(C)C)C(=O)OC(C#N)C(C=1)=CC=CC=1OC1=CC=CC=C1 NYPJDWWKZLNGGM-UHFFFAOYSA-N 0.000 description 3
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- 150000002576 ketones Chemical class 0.000 description 3
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- NBVXSUQYWXRMNV-UHFFFAOYSA-N monofluoromethane Natural products FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 3
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- 235000012222 talc Nutrition 0.000 description 1
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- 239000005936 tau-Fluvalinate Substances 0.000 description 1
- INISTDXBRIBGOC-XMMISQBUSA-N tau-fluvalinate Chemical compound N([C@H](C(C)C)C(=O)OC(C#N)C=1C=C(OC=2C=CC=CC=2)C=CC=1)C1=CC=C(C(F)(F)F)C=C1Cl INISTDXBRIBGOC-XMMISQBUSA-N 0.000 description 1
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- CJDWRQLODFKPEL-UHFFFAOYSA-N teflubenzuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC(Cl)=C(F)C(Cl)=C1F CJDWRQLODFKPEL-UHFFFAOYSA-N 0.000 description 1
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- QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical group COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 description 1
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- DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-UHFFFAOYSA-N 0.000 description 1
- RROQIUMZODEXOR-UHFFFAOYSA-N triforine Chemical compound O=CNC(C(Cl)(Cl)Cl)N1CCN(C(NC=O)C(Cl)(Cl)Cl)CC1 RROQIUMZODEXOR-UHFFFAOYSA-N 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
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- 150000003751 zinc Chemical class 0.000 description 1
- AMHNZOICSMBGDH-UHFFFAOYSA-L zineb Chemical compound [Zn+2].[S-]C(=S)NCCNC([S-])=S AMHNZOICSMBGDH-UHFFFAOYSA-L 0.000 description 1
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 description 1
Classifications
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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
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- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/44—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
- A01N37/50—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids the nitrogen atom being doubly bound to the carbon skeleton
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- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
- A01N43/08—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings with oxygen as the ring hetero atom
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- A—HUMAN NECESSITIES
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- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
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- A01N43/10—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings with sulfur as the ring hetero atom
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- A—HUMAN NECESSITIES
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- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
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- A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
- A01N43/12—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings condensed with a carbocyclic ring
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- A—HUMAN NECESSITIES
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- 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
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/36—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings
- A01N43/38—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings condensed with carbocyclic rings
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- A—HUMAN NECESSITIES
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- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
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- A—HUMAN NECESSITIES
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- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
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- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C251/00—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton
- C07C251/32—Oximes
- C07C251/34—Oximes with oxygen atoms of oxyimino groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
- C07C251/48—Oximes with oxygen atoms of oxyimino groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals with the carbon atom of at least one of the oxyimino groups bound to a carbon atom of a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/01—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms
- C07C255/32—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring
- C07C255/42—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring the carbon skeleton being further substituted by singly-bound nitrogen atoms, not being further bound to other hetero atoms
- C07C255/44—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring the carbon skeleton being further substituted by singly-bound nitrogen atoms, not being further bound to other hetero atoms at least one of the singly-bound nitrogen atoms being acylated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/62—Carboxylic acid nitriles containing cyano groups and oxygen atoms being part of oxyimino groups bound to the same carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/50—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton
- C07C323/62—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atom of at least one of the thio groups bound to a carbon atom of a six-membered aromatic ring of the carbon skeleton
- C07C323/63—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atom of at least one of the thio groups bound to a carbon atom of a six-membered aromatic ring of the carbon skeleton the carbon skeleton being further substituted by nitrogen atoms, not being part of nitro or nitroso groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
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Abstract
本发明涉及新的烷氧基亚氨基乙酰胺类化合物,其多种制备方法和其作为有害生物防治剂的应用。
Description
本发明涉及新的烷氧基亚氨基乙酰胺、其多种制备方法和其作为有害生物防治剂的应用。
业已发现通式(I)的新化合物其中A 代表单键或任选取代的亚烷基,Q 代表氧或硫,R1 代表各任选取代的环烷基、环烯基、芳基或杂环基,R2和R3相同或不同且各代表氢或各任选取代的烷基、链烯基、炔基或环烷基,R4 代表各任选取代的环烷基、环烯基、芳基或杂环基。
在定义中,饱和或不饱和烃链,如烷基、烷二基、链烯基或炔基,包括当与杂原子相连时的烃链,如烷氧基、烷硫基或烷基氨基,都是直链或支链的。
卤素一般代表氟、氯、溴或碘,优选氟、氯或溴,特别是氟或氯。
芳基代表芳族的单或多环烃环,如苯基、萘基、蒽基或菲基,优选苯基或萘基,特别是苯基。
杂环代表饱和或不饱和的芳族环化合物,其中至少一个环原子是杂原子,即不同于碳的原子。如果环含有几个杂原子,则它们可以相同或不同。杂原子优选是氧、氮或硫。
环化合物任选与另外碳环的或杂环的稠或桥环一起形成多环体系。优选的是单或二环体系,特别是单或二环芳环体系。
环烷基代表饱和的碳环化合物,它任选与另外的碳环的稠或桥环一起形成多环。
环烯基代表含有至少一个双键的碳环化合物,且任选与另外的碳环的稠或桥环一起形成多环。
最后,业已发现,新的通式(I)烷氧基亚氨基乙酰胺具有非常强的杀真菌作用。
需要时,本发明化合物是各种可能的异构体形式的混合物,特别是立体异构体,如E和Z、苏型和赤型和光学异构体。本文描述且要求保护E和Z异构体、苏型和赤型异构体以及光学异构体和这些异构体的任何所需混合物。
本发明优选涉及式(I)化合物,其中A 代表单键,或代表具有1至6个碳原子的亚烷基,它任选由相同或
不同的取代基单或多取代,可能的取代基优选选自下列:
卤素、氰基、硝基、氨基、羟基、甲酰基、羧基、氨基甲酰基或硫
代氨基甲酰基;
直链或支链烷氧基、烷硫基、烷基亚磺酰基或烷基磺酰基,它们各
具有1至6个碳原子;
直链或支链链烯基或链烯氧基,它们各具有2至6个碳原子;
直链或支链卤代烷氧基、卤代烷硫基、卤代烷基亚磺酰基或卤代烷
基磺酰基,它们各具有1至6个碳原子和1至13个相同或不同的卤
原子;
直链或支链卤代链烯基或卤代链烯氧基,它们各具有2至6个碳原
子和1至13个相同或不同的卤原子;
直链或支链烷基氨基、二烷基氨基、烷基羰基、烷基羰氧基、烷氧
基羰基、烷基磺酰氧基、肟基烷基或烷氧基亚氨基烷基,它们各在
其每一烷基部分具有1至6个碳原子;
具有3至6个碳原子的环烷基;
和取代的芳基或杂环基,它们各任选以相同或不同的方式由下列取
代基单或多取代:
卤素、氰基和/或具有1至4个碳原子的直链或支链烷基,
和/或具有1至4个碳原子和1至9个相同或不同卤原子的直链或支
链卤代烷基,
和/或具有1至4个碳原子的直链或支链烷氧基或烷硫基,
和/或具有1至4个碳原子和1至9个相同或不同卤原子的直链或支
链卤代烷氧基或卤代烷硫基,
和/或二价亚烷基或亚烷二氧基,它们各具有1至6个碳原子且任选
以相同或不同的方式由下列基团单或多取代:卤素和/或具有1至4
个碳原子的直链或支链烷基和/或具有1至4个碳原子和1至9个相
同或不同卤原子的直链或支链卤代烷基,Q 代表氧或硫,R1 代表芳基、具有3至7个碳原子的环烷基或环烯基或具有3至12
个环原子的杂环基,它们各任选由相同或不同的取代基单或多取
代,可能的取代基优选选自下列:
卤素、氰基、硝基、氨基、羟基、甲酰基、羧基、氨基甲酰基或硫
代氨基甲酰基;
直链或支链烷基、烷氧基、烷硫基、烷基亚磺酰基或烷基磺酰基,
它们各具有1至8个碳原子;
直链或支链链烯基或链烯氧基,它们各具有2至6个碳原子;
直链或支链卤代烷基、卤代烷氧基、卤代烷硫基、卤代烷基亚磺酰
基或卤代烷基磺酰基,它们各具有1至6个碳原子和1至13个相同
或不同的卤原子;
直链或支链卤代链烯基或卤代链烯氧基,它们各具有2至6个碳原
子和1至13个相同或不同的卤原子;
直链或支链烷基氨基、二烷基氨基、烷基羰基、烷基羰氧基、烷氧
基羰基、烷基磺酰氧基、肟基烷基或烷氧基亚氨基烷基,它们各在
其每一烷基部分具有1至8个碳原子;
二价亚烷基或亚烷二氧基,它们各具有1至6个碳原子且任选以相
同或不同的方式由下列基团单或多取代:卤素和/或具有1至4个碳
原子的直链或支链烷基和/或具有1至4个碳原子和1至9个相同或
不同卤原子的直链或支链卤代烷基,
具有3至6个碳原子的环烷基;
和取代的芳基、芳氧基、芳硫基、芳烷基、芳基烷氧基、芳基烷硫
基、杂环基、杂环基氧基、杂环基硫基、杂环基烷基、杂环基烷氧
基或杂环基烷硫基,它们各任选以相同或不同的方式由下列基团单
或多取代:
卤素、氰基和/或具有1至4个碳原子的直链或支链烷基,
和/或具有1至4个碳原子和1至9个相同或不同卤原子的直链或支
链卤代烷基,
和/或具有1至4个碳原子的直链或支链烷氧基或烷硫基,
和/或具有1至4个碳原子和1至9个相同或不同卤原子的直链或支
链卤代烷氧基或卤代烷硫基,
和/或二价亚烷基或亚烷二氧基,它们各具有1至6个碳原子且任选
以相同或不同的方式由下列基团单或多取代:卤素和/或具有1至4
个碳原子的直链或支链烷基和/或具有1至4个碳原子和1至9个相
同或不同卤原子的直链或支链卤代烷基,R2 代表氢,或代表具有1至4个碳原子的烷基,各具有2至4个碳原
子的链烯基或炔基或具有3至6个碳原子的环烷基,它们各任选以
相同或不同的方式由下列基团单或多取代:卤素、氰基、羟基、氨
基、C1-C4-烷氧基、C1-C4-烷硫基、C1-C4-烷基亚磺酰基或C1-
C4-烷基磺酰基(它们各任选由卤素取代)或由任选取代的苯基取
代,R3 代表氢或代表具有1至4个碳原子的烷基,R4 代表芳基、具有3至8个碳原子的环烷基或环烯基或具有3至12
个环原子的杂环基,它们各任选由相同或不同的取代基单或多取
代,可能的取代基优选选自下列:
卤素、氰基、硝基、氨基、羟基、甲酰基、羧基、氨基甲酰基或硫
代氨基甲酰基;
直链或支链烷基、烷氧基、烷硫基、烷基亚磺酰基或烷基磺酰基,
它们各具有1至6个碳原子;
直链或支链链烯基或链烯氧基,它们各具有2至6个碳原子;
直链或支链卤代烷基、卤代烷氧基、卤代烷硫基、卤代烷基亚磺酰
基或卤代烷基磺酰基,它们各具有1至6个碳原子和1至13个相同
或不同的卤原子;
直链或支链卤代链烯基或卤代链烯氧基,它们各具有2至6个碳原
子和1至13个相同或不同的卤原子;
直链或支链烷基氨基、二烷基氨基、烷基羰基、烷基羰氧基、烷氧
基羰基、烷基磺酰氧基、肟基烷基或烷氧基亚氨基烷基,它们各在
其每一烷基部分具有1至6个碳原子;
二价亚烷基或亚烷二氧基,它们各具有1至6个碳原子且任选以相
同或不同的方式由下列基团单或多取代:卤素和/或具有1至4个碳
原子的直链或支链烷基和/或具有1至4个碳原子和1至9个相同或
不同卤原子的直链或支链卤代烷基,
具有3至6个碳原子的环烷基;
和取代的芳基、芳氧基、芳硫基、芳烷基、芳基烷氧基、芳基烷硫
基、杂环基、杂环基氧基、杂环基硫基、杂环基烷基、杂环基烷氧
基或杂环基烷硫基,它们各任选以相同或不同的方式由下列基团取
代基单或多取代:
卤素、氰基和/或具有1至4个碳原子的直链或支链烷基,
和/或具有1至4个碳原子和1至9个相同或不同的卤原子的直链或
支链卤代烷基,
和/或具有1至4个碳原子的直链或支链烷氧基或烷硫基,
和/或具有1至4个碳原子和1至9个相同或不同卤原子的直链或支
链卤代烷氧基或卤代烷硫基,
和/或二价亚烷基或亚烷二氧基,它们各具有1至6个碳原子且任选
以相同或不同的方式由下列基团单或多取代:卤素和/或具有1至4
个碳原子的直链或支链烷基和/或具有1至4个碳原子和1至9个相
同或不同的卤原子的直链或支链卤代烷基。
本发明特别涉及式(I)化合物,其中A 代表单键,或代表亚甲基、1,1-亚乙基、1,2-亚乙基、1,1-、
1,2-、1,3-或2,2-亚丙基、1,1-、1,2-、1,3-、1,4-、2,2-、2,3-亚丁
基或1,1-、1,2-或1,3-(2-甲基亚丙基),它们任选以相同或不同
的方式由下列基团单或多取代:氟、氯、氰基或甲氧基,Q 代表氧或硫,R1 代表环丙基、环丁基、环戊基或环己基、苯基、萘基、呋喃基、苯
并呋喃基、吡咯基、吲哚基、噻吩基、苯并噻吩基、噁唑基、异噁
唑基、噻唑基、异噻唑基、噁二唑基、噻二唑基、吡啶基、喹啉基、
嘧啶基、哒嗪基、吡嗪基、环氧乙烷基、氧杂环丁烷基、四氢呋喃
基、全氢吡喃基、吡咯烷基、哌啶基或吗啉基,它们各任选被单至
三取代,可能的取代基优选选自下列:
氟、氯、溴、氰基、硝基、氨基、羟基、甲酰基、羧基、氨基甲酰
基、硫代氨基甲酰基、甲基、乙基、正-或异-丙基、正-、异-、仲-
或叔-丁基、正戊基、正己基、正庚基、甲氧基、乙氧基、正-或异-
丙氧基、甲硫基、乙硫基、正-或异-丙硫基、甲基亚磺酰基、乙基
亚磺酰基、甲磺酰基或乙磺酰基、三氟甲基、三氟乙基、二氟甲氧
基、三氟甲氧基、二氟氯甲氧基、三氟乙氧基、二氟甲硫基、二氟
氯甲硫基、三氟甲硫基、三氟甲基亚磺酰基或三氟甲磺酰基、甲氨
基、乙氨基、正-或异-丙氨基、二甲氨基、二乙氨基、乙酰基、丙
酰基、乙酰氧基、甲氧羰基、乙氧羰基、甲基磺酰氧基、乙基磺酰
氧基、肟基甲基、肟基乙基、甲氧基亚氨基甲基、乙氧基亚氨基甲
基、甲氧基亚氨基乙基或乙氧基亚氨基乙基;
二价三亚甲基(丙-1,3-二基)、四亚甲基(丁-1,4-二基)、亚甲
二氧基或亚乙二氧基,它们各任选以相同或不同的方式由下列基团
单或多取代:氟、氯、甲基、三氟甲基、乙基或正-或异-丙基;
环丙基、环丁基、环戊基或环己基;
苯基、苄基、苯氧基和苄氧基,它们任选由上面提及的取代基取代;R2 代表氢,或代表甲基、乙基、正-或异-丙基、或正-、异-、仲-或叔-
丁基,或代表苄基或炔丙基或烯丙基,R3 代表氢,或代表甲基或乙基,R4 代表环丙基、环丁基、环戊基或环己基、苯基、萘基、呋喃基、苯
并呋喃基、吡咯基、吲哚基、噻吩基、苯并噻吩基、噁唑基、异噁
唑基、噻唑基、异噻唑基、噁二唑基、噻二唑基、吡啶基、喹啉基、
嘧啶基、哒嗪基、吡嗪基、环氧乙烷基、氧杂环丁烷基、四氢呋喃
基、全氢吡喃基、吡咯烷基、哌啶基或吗啉基,它们各任选被单至
三取代,可能的取代基优选选自下列:
氟、氯、溴、氰基、硝基、氨基、羟基、甲酰基、羧基、氨基甲酰
基、硫代氨基甲酰基、甲基、乙基、正-或异-丙基、正-、异-、仲-
或叔-丁基、甲氧基、乙氧基、正-或异-丙氧基、甲硫基、乙硫基、
正-或异-丙硫基、甲基亚磺酰基、乙基亚磺酰基、甲磺酰基或乙磺
酰基、三氟甲基、三氟乙基、二氟甲氧基、三氟甲氧基、二氟氯甲
氧基、三氟乙氧基、二氟甲硫基、二氟氯甲硫基、三氟甲硫基、三
氟甲基亚磺酰基或三氟甲磺酰基、甲氨基、乙氨基、正或异丙氨基、
二甲氨基、二乙氨基、乙酰基、丙酰基、乙酰氧基、甲氧羰基、乙
氧羰基、甲基磺酰氧基、乙基磺酰氧基、肟基甲基、肟基乙基、甲
氧基亚氨基甲基、乙氧基亚氨基甲基、甲氧基亚氨基乙基或乙氧基
亚氨基乙基;
二价三亚甲基(丙-1,3-二基)、四亚甲基(丁-1,4-二基)、亚甲
二氧基或亚乙二氧基,它们各任选以相同或不同的方式由下列基团
单或多取代:氟、氯、甲基、三氟甲基、乙基或正-或异-丙基;
环丙基、环丁基、环戊基或环己基。
特别优选的式(I)化合物中,A 代表单键,或代表亚甲基、1,1-亚乙基、1,2-亚乙基、1,1-、
1,2-、1,3-或2,2-亚丙基、1,1-、1,2-、1,3-、1,4-、2,2-、2,3-亚丁
基或1,1-、1,2-或1,3-(2-甲基亚丙基),它们任选以相同或不同
的方式由下列单或多取代:氟、氯、氰基或甲氧基,Q 代表氧或硫,R1 代表环丁基、环戊基或环己基,它们各任选被单至六取代,优选的
取代基是下文提及的那些取代基,
或代表苯基、萘基、呋喃基、苯并呋喃基、噻吩基、苯并噻吩基、
吡啶基、喹啉基、四氢呋喃基或全氢吡喃基,它们各任选被单至三
取代,可能的取代基优选选自下列:
氟、氯、溴、氰基、硝基、甲基、乙基、正-或异-丙基、正-、异-、
仲-或叔-丁基、正戊基、正己基、正庚基、甲氧基、乙氧基、正-或
异-丙氧基、甲硫基、乙硫基、正-或异-丙硫基、甲基亚磺酰基、乙
基亚磺酰基、甲磺酰基或乙磺酰基、三氟甲基、三氟乙基、二氟甲
氧基、三氟甲氧基、二氟氯甲氧基、三氟乙氧基、二氟甲硫基、二
氟氯甲硫基、三氟甲硫基、三氟甲基亚磺酰基、三氟甲磺酰基、乙
酰基、丙酰基、乙酰氧基、甲氧羰基、乙氧羰基、甲基磺酰氧基、
乙基磺酰氧基、肟基甲基、肟基乙基、甲氧基亚氨基甲基、乙氧基
亚氨基甲基、甲氧基亚氨基乙基或乙氧基亚氨基乙基;
二价三亚甲基(丙-1,3-二基)、四亚甲基(丁-1,4-二基)、亚甲
二氧基或亚乙二氧基,它们各任选以相同或不同的方式由下列基团
单或多取代:氟、氯、甲基、三氟甲基、乙基或正-或异-丙基;
环丙基、环戊基或环己基;
苯基、苯氧基和苄氧基,它们任选由上文提及的取代基取代;R2 代表氢,或代表甲基、乙基、正或异丙基、或正、异或叔丁基,
代表苄基或烯丙基,R3 代表氢或甲基,R4 代表环丙基、环丁基、环戊基或环己基,它们各任选单至六取代,
优选的取代基是下文提及的那些取代基;
或代表苯基、萘基、呋喃基、苯并呋喃基、吡咯基、吲哚基、噻吩
基、苯并噻吩基、噁唑基、异噁唑基、噻唑基、异噻唑基、噁二唑
基、噻二唑基、吡啶基、喹啉基、嘧啶基、哒嗪基、吡嗪基、环氧
乙烷基、氧杂环丁烷基、四氢呋喃基、全氢吡喃基、吡咯烷基、哌
啶基或吗啉基,它们各任选单至三取代,可能的取代基优选选自下
列:
氟、氯、溴、氰基、硝基、氨基、羟基、甲酰基、羧基、氨基甲酰
基、硫代氨基甲酰基、甲基、乙基、正-或异-丙基、正-、异-、仲-
或叔-丁基、甲氧基、乙氧基、正-或异-丙氧基、甲硫基、乙硫基、
正-或异-丙硫基、甲基亚磺酰基、乙基亚磺酰基、甲磺酰基或乙磺
酰基、三氟甲基、三氟乙基、二氟甲氧基、三氟甲氧基、二氟氯甲
氧基、三氟乙氧基、二氟甲硫基、二氟氯甲硫基、三氟甲硫基、三
氟甲基亚磺酰基或三氟甲磺酰基、甲氨基、乙氨基、正-或异-丙
氨基、二甲氨基、二乙氨基、乙酰基、丙酰基、乙酰氧基、甲氧羰
基、乙氧羰基、甲基磺酰氧基、乙基磺酰氧基、肟基甲基、肟基乙
基、甲氧基亚氨基甲基、乙氧基亚氨基甲基、甲氧基亚氨基乙基或
乙氧基亚氨基乙基;
二价三亚甲基(丙-1,3-二基)、四亚甲基(丁-1,4-二基)、亚甲
二氧基或亚乙二氧基,它们各任选以相同或不同的方式由下列基团
单或多取代:氟、氯、甲基、三氟甲基、乙基或正-或异-丙基;
环丙基、环丁基、环戊基或环己基。
特别优选的本发明化合物组是式(I)化合物,其中A 代表单键,或代表亚甲基、1,1-亚乙基、1,2-亚乙基、1,1-亚丙基、
1,2-亚丙基、1,3-亚丙基或2,2-亚丙基,Q 代表氧,R1 代表苯基、噻吩基或呋喃基,它们任选由下列基团单或二取代:
溴、氯、氟、硝基、甲磺酰基、苯基、苯氧基、苄氧基、环丙基、
环己基、甲基、乙基、正-或异-丙基、正-、异-、仲-或叔-丁基、正
戊基、正己基、正庚基、甲氧基、乙氧基、三氟甲基、三氟甲氧基
和/或甲硫基,
或代表苯基,该苯基由各任选被氟取代的3,4-亚甲基-和亚乙二氧
基、丙-1,3-二基或丁-1,4-二基取代,
或代表萘基、苯并呋喃基或苯并噻吩基,R2 代表氢、甲基或乙基,或代表正-或异-丙基,或代表正-、异-、仲-
或叔-丁基,或代表苄基或烯丙基,R3 代表氢或甲基,R4 代表环己基或任选单至三取代的苯基、噻吩基、呋喃基、苯并呋喃
基、苯并噻吩基、吡啶基、嘧啶基、萘基或喹啉基,可能的取代基
优选选自下列:
氟、氯、溴、氰基、硝基、氨基、羟基、甲酰基、羧基、氨基甲酰
基、硫代氨基甲酰基、甲基、乙基、正-或异-丙基、正-、异-、仲-
或叔-丁基、甲氧基、乙氧基、正-或异-丙氧基、甲硫基、乙硫基、
正-或异-丙硫基、甲基亚磺酰基、乙基亚磺酰基、甲磺酰基或乙磺
酰基、三氟甲基、三氟乙基、二氟甲氧基、三氟甲氧基、二氟氯甲
氧基、三氟乙氧基、二氟甲硫基、二氟氯甲硫基、三氟甲硫基、三
氟甲基亚磺酰基或三氟甲磺酰基、甲氨基、乙氨基、正-或异-丙
氨基、二甲氨基、二乙氨基、乙酰基、丙酰基、乙酰氧基、甲氧羰
基、乙氧羰基、甲基磺酰氧基、乙基磺酰氧基、肟基甲基、肟基乙
基、甲氧基亚氨基甲基、乙氧基亚氨基甲基、甲氧基亚氨基乙基或
乙氧基亚氨基乙基;
二价三亚甲基(丙-1,3-二基)、四亚甲基(丁-1,4-二基)、亚甲
二氧基或亚乙二氧基,它们各任选以相同或不同的方式由下列基团
单或多取代:氟、氯、甲基、三氟甲基、乙基或正-或异-丙基。
特别感兴趣的式(I)化合物是那些其中R1代表如下基团的化合物:苯基,该苯基是未取代的或在3-和/或4-位上被取代;呋喃基或噻吩基,它们是未取代的或在4-和/或5-位上被取代,所选的取代基是那些上面提到的取代基,且特别是氯、溴、氟、硝基、甲磺酰基、苯基、苯氧基、苄氧基、环丙基、环己基、甲基、乙基、正-或异-丙基、正-、异-、仲-或叔-丁基、正戊基、正己基、正庚基、甲氧基、乙氧基、甲硫基、三氟甲基和三氟甲氧基;或苯基,该苯基由各任选被氟取代的3,4-亚甲基-和亚乙基二氧基、丙-1,3-二基和丁-1,4-二基取代;或萘基、苯并呋喃基或苯并噻吩基,它们在2-位上被取代。
同样特别优选式(I)化合物中,R2 代表甲基或乙基。
同样特别优选式(I)化合物中,R3 代表氢。
同样特别优选式(I)化合物中,R4代表在3-和4-位上由甲氧基取代的苯基。
上述给出的一般或优选基团定义适合于式(I)终产物,且相应地适合于在每种制备情况下所需的原料或中间体。
这些定义可以按需要相互组合,即优选化合物所述范围间的组合也是可能的。
可以由下表见到优选的单个化合物:
表1
化合物号 | R5 |
Ia-1 | 氢 |
Ia-2 | 4-氯 |
Ia-3 | 4-氟 |
Ia-4 | 4-溴 |
Ia-5 | 4-甲基 |
Ia-6 | 4-乙基 |
Ia-7 | 4-异丙基 |
Ia-8 | 4-正丙基 |
Ia-9 | 4-正丁基 |
Ia-10 | 4-异丁基 |
Ia-11 | 4-叔丁基 |
Ia-12 | 4-仲丁基 |
Ia-13 | 4-甲氧基 |
Ia-14 | 4-乙氧基 |
Ia-15 | 4-甲硫基 |
Ia-16 | 4-三氟甲基 |
Ia-17 | 3-氯 |
Ia-18 | 3-氟 |
化合物号 | R5 |
Ia-19 | 3-溴 |
Ia-20 | 3-甲基 |
Ia-21 | 3-乙基 |
Ia-22 | 3-异丙基 |
Ia-23 | 3-正丙基 |
Ia-24 | 3-正丁基 |
Ia-25 | 3-异丁基 |
Ia-26 | 3-叔丁基 |
Ia-27 | 3-仲丁基 |
Ia-28 | 3-甲氧基 |
Ia-29 | 3-乙氧基 |
Ia-30 | 3-甲硫基 |
Ia-31 | 3-三氟甲基 |
Ia-32 | 3,4-二氯 |
Ia-33 | 3,4-二氟 |
Ia-34 | 3,4-二溴 |
Ia-35 | 3,4-二甲基 |
Ia-36 | 3,4-二乙基 |
Ia-37 | 3,4-OCH2O |
Ia-38 | 3,4-OCH2CH2O |
Ia-39 | 3,4-OCF2O |
Ia-40 | 3,4-OCF2CF2O |
Ia-41 | 3,4-(CH2)3 |
Ia-42 | 3,4-(CH2)4 |
化合物号 | R5 |
Ia-43 | 3,4-二甲氧基 |
Ia-44 | 3,4-二乙氧基 |
Ia-45 | 3,4-二甲硫基 |
Ia-46 | 3,4-二-三氟甲基 |
Ia-47 | 3-氯,4-甲基 |
Ia-48 | 4-氯,3-甲基 |
Ia-49 | 3-氯,4-甲氧基 |
Ia-50 | 4-氯,3-甲氧基 |
Ia-51 | 3-氯,4-乙基 |
Ia-52 | 4-氯,3-乙基 |
Ia-53 | 3-甲氧基,4-乙氧基 |
Ia-54 | 4-甲氧基,3-乙氧基 |
Ia-55 | 3-甲基,4-甲氧基 |
Ia-56 | 4-甲基,3-甲氧基 |
Ia-57 | 3-甲基,4-乙基 |
Ia-58 | 4-甲基,3-乙基 |
Ia-59 | 3-甲氧基,4-乙基 |
Ia-60 | 4-甲氧基,3-乙基 |
Ia-61 | 4-硝基 |
Ia-62 | 4-甲磺酰基 |
Ia-63 | 4-苯氧基 |
Ia-64 | 4-苯基 |
Ia-65 | 4-苄氧基 |
Ia-66 | 4-戊基 |
Ia-67 | 4-己基 |
Ia-68 | 4-庚基 |
Ia-69 | 4-环丙基 |
Ia-70 | 4-环己基 |
表2
化合物号 | R5 |
Ib-1 | 氢 |
Ib-2 | 4-氯 |
Ib-3 | 4-氟 |
Ib-4 | 4-溴 |
Ib-5 | 4-甲基 |
Ib-6 | 4-乙基 |
Ib-7 | 4-异丙基 |
Ib-8 | 4-正丙基 |
Ib-9 | 4-正丁基 |
Ib-10 | 4-异丁基 |
Ib-11 | 4-叔丁基 |
Ib-12 | 4-仲丁基 |
Ib-13 | 4-甲氧基 |
Ib-14 | 4-乙氧基 |
Ib-15 | 4-甲硫基 |
Ib-16 | 4-三氟甲基 |
Ib-17 | 5-氯 |
Ib-18 | 5-氟 |
Ib-19 | 5-溴 |
化合物号 | R5 |
Ib-20 | 5-甲基 |
Ib-21 | 5-乙基 |
Ib-22 | 5-异丙基 |
Ib-23 | 5-正丙基 |
Ib-24 | 5-正丁基 |
Ib-25 | 5-异丁基 |
Ib-26 | 5-仲丁基 |
Ib-27 | 5-叔丁基 |
Ib-28 | 5-甲氧基 |
Ib-29 | 5-乙氧基 |
Ib-30 | 5-甲硫基 |
Ib-31 | 5-三氟甲基 |
Ib-32 | 4,5-二氯 |
Ib-33 | 4,5-二氟 |
Ib-34 | 4,5-二溴 |
Ib-35 | 4,5-二甲基 |
Ib-36 | 4,5-二乙基 |
Ib-37 | 4,5-二甲氧基 |
Ib-38 | 4,5-二-三氟甲基 |
Ib-39 | 4-氯,5-甲基 |
Ib-40 | 5-氯,4-甲基 |
表3
化合物号 | R5 |
Ic-1 | 氢 |
Ic-2 | 4-氯 |
Ic-3 | 4-氟 |
Ic-4 | 4-溴 |
Ic-5 | 4-甲基 |
Ic-6 | 4-乙基 |
Ic-7 | 4-异丙基 |
Ic-8 | 4-正丙基 |
Ic-9 | 4-正丁基 |
Ic-10 | 4-异丁基 |
Ic-11 | 4-叔丁基 |
Ic-12 | 4-仲丁基 |
Ic-13 | 4-甲氧基 |
Ic-14 | 4-乙氧基 |
Ic-15 | 4-甲硫基 |
Ic-16 | 4-三氟甲基 |
Ic-17 | 5-氯 |
Ic-18 | 5-氟 |
化合物号 | R5 |
Ic-19 | 5-溴 |
Ic-20 | 5-甲基 |
Ic-21 | 5-乙基 |
Ic-22 | 5-异丙基 |
Ic-23 | 5-正丙基 |
Ic-24 | 5-正丁基 |
Ic-25 | 5-异丁基 |
Ic-26 | 5-仲丁基 |
Ic-27 | 5-叔丁基 |
Ic-28 | 5-甲氧基 |
Ic-29 | 5-乙氧基 |
Ic-30 | 5-甲硫基 |
Ic-31 | 5-三氟甲基 |
Ic-32 | 4,5-二氯 |
Ic-33 | 4,5-二氟 |
Ic-34 | 4,5-二溴 |
Ic-35 | 4,5-二甲基 |
Ic-36 | 4,5-二乙基 |
Ic-37 | 4,5-二甲氧基 |
Ic-38 | 4,5-二-三氟甲基 |
Ic-39 | 4-氯,5-甲基 |
Ic-40 | 5-氯,4-甲基 |
化合物Ia-1至Id-3相应于式Ia、Ib、Ic和Id,其中3,4-二甲氧基苯基(一般标示为R4)由苯基替代,所述的苯基带有在化合物Ia-1至Ia-70中作为R5所述的取代基。表6
化合物Ia-1至Id-3相应于式Ia、Ib、Ic和Id,其中3,4-二甲氧基苯基(一般标示为R4)由下列三取代的苯基之一替代:取代基:3,4,5-三甲氧基;3,4,5-三氯;3,4,5-三甲基。表7
化合物Ia-1至Id-3相应于式Ia、Ib、Ic和Id,其中甲氧基亚氨基(一般标示为R2)由乙氧基亚氨基替代,所述的乙氧基亚氨基带有在化合物Ia-1至Ia-70中作为R5所述的取代基。
还发现,新的通式(I)的烷氧基亚氨基乙酰胺可以通过如下方法获得:使通式(II)的羧酸衍生物其中R1、R2和Q具有上述含义,且T 代表羟基、卤素或烷氧基,如果需要在酸接受体存在下,如果需要在缩合剂存在下,如果需要在稀释剂存在下,与通式(III)的胺或与其氢卤化物反应,其中R3、R4和A具有上述含义。
式(II)提供了进行本发明方法所需原料羧酸衍生物的一般定义。在此式(II)中,(Q、R1和R2)优选或特别是具有与本发明式(I)化合物描述相关的定义中已经给出的优选或特别优选的(Q、R1和R2)的含义。T优选代表具有1至4个碳原子的烷氧基,特别是甲氧基或乙氧基,或代表羟基或氯。
式(II)的原料是已知的和/或可以通过已知的方法制备(参见,EP-A 178 826、EP-A 242 081、EP-A 382 375、EP-A 493711、EP-A 432 503、DE 3 938 054)。
式(III)提供了另一种原料胺的一般定义。
式(III)的原料是已知的有机合成化学品和/或可以通过本身已知的方法制备。
如果需要,本发明的方法是在酸受体存在下进行的。适合的酸受体是所有的常规无机或有机碱。这些碱是例如:碱金属或碱土金属氢化物、氢氧化物、氨化物、醇化物、乙酸盐、碳酸盐或碳酸氢盐,如氢化钠、氨化钠、甲醇钠、乙醇钠、叔丁醇钾、氢氧化钠、氢氧化钾、氢氧化铵、乙酸钠、乙酸钾、乙酸钙、乙酸铵、碳酸钠、碳酸钾、碳酸氢钾、碳酸氢钠或碳酸铵,以及叔胺如三甲胺、三乙胺、三丁胺、N,N-二甲基苯胺、N,N-二甲基苄胺、吡啶、N-甲基哌啶、N,N-二甲基氨基吡啶、二氮杂双环辛烷(DABCO)、二氮杂双环壬烯(DBN)和二氮杂双环十一碳烯(DBU)。
如果需要,本发明是在适合的缩合剂存在下进行的。可能的缩合剂是所有的通常可以用于这种酰胺化反应的缩合剂。可以提到的形成酰基卤的试剂实例有,例如,光气、三溴化磷、三氯化磷、五氯化磷、磷酰氯或亚磺酰氯;形成酸酐的试剂例如,氯甲酸乙酯、氯甲酸甲酯或甲磺酰氯;碳化二亚胺,如N,N’-二环己基碳化二亚胺(DCC)、或其它常规缩合剂,如五氧化磷、多磷酸、N,N’-羰基二咪唑、2-乙氧基-N-乙氧基羰基-1,2-二氢喹啉(EEDQ)或三苯基膦/四氯化碳。
如果需要,本发明的方法是在稀释剂存在下进行。进行本发明方法的可能的稀释剂是水或有机溶剂。这些溶剂包括特别是脂族、脂环族或芳族、任选卤代的烃类,如,汽油、苯、甲苯、二甲苯、氯苯、二氯苯、石油醚、己烷、环己烷、二氯甲烷、氯仿、四氯化碳;醚类,如,***、二异丙醚、二噁烷、四氢呋喃或乙二醇二甲基或二乙基醚;酮类,如,丙酮、丁酮或甲基异丁基酮;腈类,如,乙腈、丙腈或苯甲腈;酰胺类,如N,N-二甲基甲酰胺、N,N-二甲基乙酰胺、N-甲基甲酰苯胺、N-甲基吡咯烷酮或六甲基磷酰三胺;酯类,如,乙酸甲酯或乙酸乙酯;亚砜类,如二甲亚砜;醇类,如甲醇、乙醇、正或异丙醇、乙二醇、乙二醇单甲醚、乙二醇单***、二乙二醇单甲醚、二乙二醇单***、其与水的混合物或在纯水中进行。
进行本发明方法时,反应温度可以在相当宽的范围内变化。-般而言,反应是在-20℃和+200℃之间的温度下进行。优选是在0℃与150℃间的温度下进行的。
进行本发明方法时,每摩尔式(II)羧酸衍生物,一般采用1至5摩尔,优选1.0至2.5摩尔的胺。
反应的进行以及反应产物的收集和分离是通过已知的方法来完成的(参见制备实施例)。
如果需要,本发明的反应在催化剂存在下进行。可以提到的催化剂的实例是4-二甲基氨基吡啶、1-羟基-苯并***或二甲基甲酰胺。
反应温度可以在相当宽的范围内变化。一般而言,反应是在-78℃和+120℃之间的温度下进行。优选是在-60℃与+25℃间的温度下进行的。
进行制备式(I)化合物的本发明方法时,每摩尔式(II)烷氧基亚氨基羧酸衍生物,一般采用0.5至5摩尔,优选等摩尔量的式(III)胺。
反应的进行以及反应产物的收集和分离是通过已知的方法来完成的(参见制备实施例)。
本发明的方法也可以分二个阶段进行。在这种情况下,首先将通式(II)的羧酸衍生物转化成活化的形式,并在随后的步骤中,与通式(III)的胺反应,生成本发明通式(I)的烷氧基亚氨基乙酸衍生物。
式(II)羧酸衍生物的活化形式是所有的羧基活化衍生物,如酰基卤,优选酰基氯,酰基叠氮以及对称或混合的酸酐,如混合的O-烷基羧酸酐,和活化的酯,如对硝基苯基酯或N-羟基琥珀酰亚胺酯,以及与缩合剂如二环己基碳化二亚胺的加成物,或现场产生的羧酸活化形式。
本发明的活性化合物具有强的杀微生物活性,且可以实际上用来防治有害微生物。本发明活性化合物适合用作植物保护剂,特别是杀真菌剂。
杀真菌剂采用在植物保护中,用于防治根肿菌纲,卵菌纲,壶菌纲,接合菌纲,子囊菌纲,担子菌纲和半知菌类。
上面列出的某些病原真菌病害以属名给出,可以提到的有例如下列,但决不限于此:腐霉属,如终极腐霉(Pythium ultimum);疫霉属,如蔓延疫霉(Phytophthora infestans);假霜霉属,如律草假霜霉(Pseudoperonospora humuli)或古巴假霜霉(P.cubensis);单轴霉属,如葡萄生单轴霉(Plasmopara viticola);霜霉属,如豌豆霜霉(Peronospora pisi)或芸苔霜霉(P.brassicae);白粉菌属,如禾白粉菌(Erysiphe graminis);单丝壳属,如苍耳单丝壳菌(Sphaerotheca fuliginea);柄球菌属,如苹果白粉病柄球菌(Podosphaera leucotricha);黑星菌属,如苹果黑星菌(Venturia inaequalis);核腔菌属,如圆核腔菌(Pyrenophora teres)或麦类核腔菌(P.graminea)(分生孢子形式:Drechslera,异名:长蠕孢属(Helminthosporium));旋孢腔菌属,如禾旋孢腔菌(Cochliobolus sativus)(分生孢子形式:Drechslera,异名:长蠕孢属(Helminthosporium));单孢锈属,如菜豆单孢锈菌(Uromyces appendiculatus);柄锈属,如隐匿柄锈菌(Puccinia recondita);腥黑粉菌属,如小麦网腥黑粉菌(Tilletia caries);黑粉菌属,如裸黑粉菌(Ustilago nuda)或燕麦散黑粉菌(U.avenae);薄膜革菌属,如佐佐木氏薄膜革菌(Pellicularia sasakii);梨孢菌属,如稻梨孢菌(Pyricularia oryzae);镰孢属,如大刀镰孢(Fusarium culmorum);葡萄孢属,如灰色葡萄孢(Botrytis cinerea);壳针孢属,如颖枯壳针孢(Septoria nodorum);小球腔菌属,如颍枯病小球腔菌(Leptosphaeria nodorum);尾孢属,如变灰尾孢菌(Cercospora canescens);链格孢属,如甘蓝黑斑病链格孢菌(Alternaria brassicae),和假小尾孢菌属,如麦类眼斑病菌(Pseudocercosporalla herpotrichoides)。
在防治植物病害所需浓度下,植物对活性化合物的良好耐药性,使活性化合物可以处理植物的地上部分、无性繁殖根茎和种子以及土壤。
本发明的活性化合物可以特别成功地用于防治葡萄、果树和蔬菜种植中的病害,如防治单轴霉和疫霉菌属种类引起的病害。
根据其具体的物理和/或化学特性,活性化合物可以转化成常规剂型,如溶液、乳剂、悬浮剂、粉剂、泡沫剂、膏剂、颗粒剂、气雾剂、聚合物中的细微胶囊和转化成种子包衣组合物、以及ULV冷和热雾剂。
这些型剂可以用已知的方式生产,例如,将活性化合物与填充剂(即液体溶剂、压力下的液化气体)混合,和/或与固体载体混合,并任选使用表面活性剂(即乳化剂和/或分散剂和/或起泡剂)。用水作填充剂的情况下,也可以用有机溶剂作助溶剂。作为液体溶剂,适合的主要有:芳族化合物,如二甲苯,甲苯或烷基萘,氯代芳族化合物或氯代脂肪烃,如氯代苯类、氯乙烯类或二氯甲烷,脂族烃,如环己烷或石蜡,例如矿物油馏份,醇类,如丁醇或乙二醇以及其醚和酯,酮类,如丙酮、甲乙酮、甲基异丁基酮或环己酮,强极性溶剂,如二甲基甲酰胺或二甲亚砜,以及水;液化气填充剂或载体是指常温和常压下是气体的液体,例如气雾抛射剂,如卤代烃及丁烷、丙烷、氮气和二氧化碳;固体载体适合的有:磨碎的天然矿物质如高岭土、粘土、滑石、白垩、石英、硅镁土、蒙脱石或硅藻土,和磨碎的合成矿物质,如高分散二氧化硅、矾土和硅酸盐;用于颗粒剂的固体载体适合的有:例如压碎和破碎的天然矿物质如方解石、大理石、浮石、海泡石和白云石,以及有机和无机粉的合成颗粒,和如下有机物的颗粒:锯木屑、椰壳、玉米穗轴和烟茎;乳化剂和/或起泡剂适合的有:例如非离子和阴离子乳化剂,如聚氧乙烯脂肪酸酯、聚氧乙烯脂肪醇醚,例如,烷芳基聚乙二醇醚,烷基磺酸盐,烷基硫酸盐,芳基磺酸盐以及白蛋白水解产物;分散剂适合的有:例如,木素亚硫酸废液和甲基纤维素。
制剂中可以使用粘合剂如羧甲基纤维素和粉状、颗粒或乳胶形式的天然和合成聚合物,如***胶、聚乙烯醇和聚乙酸乙烯酯,以及天然磷脂,如脑磷脂和卵磷脂,和合成磷脂。其它的粘合剂可以是矿物油和植物油。
也可能使用染料,如无机颜料,例如氧化铁、氧化钛和普鲁士蓝,和有机染料,如茜素染料、偶氮染料和金属酞菁染料,和微量营养素如铁、锰、硼、铜、钴、钼和锌盐。
制剂中通常含有按重量计0.1至95%的活性化合物,优选0.5至90%。
本发明的活性化合物可以其本身或以其与已知的杀真菌剂、杀细菌剂、杀螨剂、杀线虫剂或杀虫剂的混合物的制剂形式使用,以扩大作用谱,或为防止抗性的逐步建立。
在许多情况下,可以获得增效作用。
适合用于混合物的组分是例如下列化合物:杀真菌剂:
2-氨基丁烷、2-苯胺基-4-甲基-6环丙基-嘧啶;2′,6′-二溴-2-甲基-4′-三氟甲氧基-4′-三氟甲基-1,3-噻唑-5-甲酰苯胺;2,6-二氯-N-(4-三氟甲基苯甲基)苯甲酰胺;(E)-2-甲氧基亚氨基-N-甲基-2-(2-苯氧苯基)乙酰胺;8-羟基喹啉硫酸盐;(E)-2-{2-[6-(2-氰基-苯氧基)嘧啶-4-氧基]苯基}-3-甲氧基丙烯酸甲酯;(E)-甲氧基亚氨基[α-(邻甲苯氧基)-邻甲苯基]乙酸甲酯;2-苯基苯酚(OPP)、aldimorph、氨丙磷酸、敌菌灵、戊环唑、苯霜灵、碘萎灵、苯菌灵、乐杀螨、联苯、双苯***醇、灭瘟素、糠菌唑、磺酸丁嘧啶、丁赛特、石硫合剂、敌菌丹、克菌丹、多菌灵、萎锈灵、甲基克杀螨、地茂散、氯化苦、百菌清、乙菌利、硫杂灵、霜脲氰、环唑醇、酯菌胺、防霉酚、苄氯***醇、抑菌灵、哒菌清、氯硝胺、乙霉威、噁醚唑、甲嘧醇、烯酰吗啉、烯唑醇、清螨普、二苯胺、吡菌硫、灭菌磷、二噻农、十二烷胍、腙菌酮、克菌散、环氧唑(epoxyconazole)、乙嘧啶、氯唑灵、双氯苯嘧啶、苯氰唑、一甲呋萎灵、种衣酯、拌种咯、苯锈啶、丁苯吗啉、乙酸三苯基锡、三苯羟基锡、福美铁、嘧菌腙、氟啶胺、fludioxonil、氟氯菌核利、fluquinconazole、氟哇唑、磺菌胺、氟酰胺、粉唑醇、灭菌丹、乙磷铝、四氯苯酞、麦穗宁、呋霜灵、拌种胺、双胍辛、六氯苯、己唑醇、甲羟异φ唑、抑霉唑、酰胺唑、双胍辛醋酸盐、异稻瘟净、异菌脲、稻瘟灵、春日霉素、铜制剂如氢氧化铜、环烷酸铜、碱式氯化铜、硫酸铜、氧化铜、喹啉酮和波尔多混合物、双代混剂、代森锰锌、代森锰、嘧菌胺、灭锈胺、甲霜灵、metconazole、磺菌威、担菌胺、代森联、噻菌胺、腈菌唑、福美镍、异丙消、氟苯嘧啶醇、甲呋酰胺、噁酰胺、oxamocarb、氧化萎锈灵、perfurazoat、戊菌唑、戊菌隆、稻病磷、匹马菌素、哌啶宁、多氧霉素、烯丙异噻唑、咪鲜安、二甲菌核利、霜霉威、丙环唑、甲基代森锌、定菌磷、啶斑肟、pyrimethanil、咯喹酮、五氯硝基苯、硫磺和硫制剂、戊唑醇、酞枯酸、四氯硝基苯、氟醚唑、噻菌灵、噻菌腈、甲基托布津、福美双、甲基立枯灵、对甲抑菌灵、***酮、***醇、唑菌嗪、杨菌胺、三环唑、环吗啉、氟菌唑、嗪氨灵、triticonazole、稻纹散、乙烯菌核利、代森锌、福美锌。杀细菌剂:
拌棉酚、防霉酚、氯定、福美镍、春日霉素、异噻菌酮、呋喃羧酸、土霉素、烯丙异噻唑、链霉素、酞枯酸、硫酸铜和其它铜制剂。杀虫剂/杀螨剂/杀线虫剂:
齐墩螨素、AC 303 630、乙酰甲胺磷、氟酯菊酯、棉铃威、涕灭威、甲体氯氰菊酯、双甲脒、齐墩螨素(avermectin)、AZ 60541、azadirachtin、乙基谷硫磷、谷硫磷、***锡、苏芸金杆菌、苯噁威、丙硫克百威、杀虫磺、乙体氟氯氰菊酯、联苯菊酯、丁苯威、溴醚菊酯(brofenprox)、溴硫磷、混戊威、噻嗪酮、丁酮威、丁基哒螨酮、硫线磷、西维因、克百威、三硫磷、丁硫克百威、巴丹、CGA 157 419、CGA 184699、除线威、chlorethoxyfos、毒虫畏、定虫隆、氯甲硫磷、毒死蜱、甲基毒死蜱、顺式苄呋菊酯、三氟氯氰菊酯、四螨嗪、杀螟腈、乙氰菊酯、氟氯氰菊酯、氯氟氰菊酯、三环锡、氯氰菊酯、灭蝇胺、溴氰菊酯、甲基内吸磷、内吸磷、异吸磷II、杀螨隆、地亚农、氯线磷、敌敌畏、dicliphos、百治磷、乙硫磷、伏虫脲、乐果、甲基毒虫畏、二噁硫磷、乙拌磷、克瘟散、emamectin、高氰戊菊酯、除蚜威、乙硫磷、醚菊酯、丙线磷、乙嘧硫磷、克线磷、喹螨醚、螨完锡、杀螟硫磷、仲丁威、苯硫威、双氧威、甲氰菊酯、fenpyrad、唑螨酯、倍硫磷、氰戊菊酯、fipronil、氟啶胺、fluazuron、氟螨脲、氟氰戊菊酯、氟虫脲、氟醚菊酯(flufenprox)、氟胺氰菊酯、地虫硫磷、安果、噻唑硫磷、溴醚菊酯(fubfenprox)、呋线成、六六六、庚虫磷、氟铃脲、噻螨酮、咪蚜胺、异稻瘟净、氯唑磷、异丙胺磷、异丙威、噁唑磷、伊维菌素、λ-三氟氯氰菊酯、lufenuron、马拉硫磷、灭蚜硫磷、速灭磷、倍硫磷亚砜、蜗牛敌、虫螨畏、甲胺磷、甲噻硫磷、甲硫威、灭多威、速灭威、米尔倍菌素、久效磷、moxidectin、二溴磷、NC 184、NI 25、nitenpyram、氧乐果、草肟威、砜吸硫磷、异砜磷、对硫磷、甲基对硫磷、氯菊酯、稻丰散、甲拌磷、伏杀硫磷、亚胺硫磷、磷胺、辛硫磷、抗蚜威、甲基嘧啶硫磷、嘧啶硫磷、丙溴磷、甲丙威、丙虫威、残杀威、低毒硫磷、发果、pymetrozin、pyrachlophos、吡唑硫磷、苯哒嗪硫磷、反灭菊酯、除虫菊、哒螨酮、pyrimidifen、蚊蝇醚、喹硫磷、RH 5992、水杨硫磷、硫线磷、silafluofen、治螟磷、甲丙硫磷、tebufenozide、tebufenpyrad、特丁嘧啶硫磷、伏虫隆、七氟菊酯、双硫磷、叔丁威、特丁甲拌磷、杀虫畏、thiafenox、硫双灭多威、己酮肟威、甲基乙拌磷、喹线磷、苏芸金菌素、四溴菊酯、苯赛螨、***磷、triazuron、敌百虫、杀虫隆、trimethacarb、完灭硫磷、二甲威、二甲苯威、zetamethrin。
如果需要,本发明的活性化合物也可与其它已知活性化合物如除草剂、或与化肥和生长调节剂混合。
活性化合物可以以其原样或以其制剂或由其制备的使用形式使用,所述的制备使用形式有例如可直接使用溶液、悬浮剂、可湿性粉剂、膏剂、可溶性粉剂、粉剂和颗粒剂。它们以常规方法使用,例如浇泼、喷雾、弥雾、撒施、喷粉、.起泡、涂刷等等。此外可用超低容量方法使用化合物,或将活性化合物制剂或活性化合物本身注入土壤。也可处理植物的种子。
处理植物部分时,使用形式中的活性化合物浓度可在大范围内变化:通常,在按重量计1和0.0001%之间,优选在按重量计0.5和0.001%间使用。
处理种子时,通常每公斤种子需要0.001至50g,优选0.01至10g量的活性化合物。
处理土壤时,在作用点需要活性化合物的浓度为按重量计0.00001至0.1%,优选按重量计0.0001至0.02%。
将1.66g(8mmol)2-甲氧基亚氨基-2-[2-(2,4-二甲基)苯基]乙酸甲酯和1.14g(8mmol)4-氯苯甲胺在120℃熔融状态下搅拌12小时。冷却后,用二氯甲烷消化,并将混合物用水洗涤,之后用1N盐酸且之后再用水洗涤,经硫酸钠干燥并过滤。将滤液在真空中浓缩,残留物用石油醚/乙酸乙酯(5∶1)作洗脱液在硅胶上色谱分离。
得1.24g(理论值的47%)的N-(4-氯苄基)-2-甲氧基亚氨基-2-[2-(2,4-二甲基)苯基]-乙酰胺,为油状物。1H-NMR(CDCl3,TMS):δ=3.95ppm(s,3H)实施例2:
在-10℃下,将2.8ml(20mmol)三乙胺和2.8g(20mmol)氯甲酸异丁酯依次滴加入4.14g(20mmol)2-甲氧基亚氨基-2-[2-(2,4-二甲基)苯基]-乙酸的80ml二氯甲烷溶液中,并将此混合物在-10℃下搅拌2小时。之后,经30分钟将2.55g(20mmol)4-氯苯胺的10ml二氯甲烷溶液滴加入,并将此混合物在-10℃搅拌2小时,并在20℃下搅拌18小时。将之在真空中浓缩,残留物用二氯甲烷消化,并将混合物用水洗涤一次,之后用1N盐酸并再用水洗涤,经硫酸钠干燥,过滤并再浓缩之。残留物用二异丙醚搅拌,将由此得的晶体滤出,并干燥。
在20℃下,经20分钟,将1.81g(8mmol)2-甲氧基亚氨基-2-(4-氯苯基)-乙酰氯滴加入1.02g(8mmol)4-氯苯胺和1.12ml(8mmol)三乙胺在30ml二氯甲烷中的混合物中,并将此混合物中20℃搅拌18小时。将之倒入水中,并先用碳酸氢钠水溶液,且之后用水洗涤。有机相经硫酸钠干燥,过滤并再浓缩之。残留物用石油醚/乙酸乙酯(5∶1)作洗脱液在硅胶上色谱分离。
在室温下,先将4.45g(20mmol)2-甲氧基亚氨基-2-(4-氯苯基)乙酸甲酯的50ml甲醇溶液导入反应容器中,依次加入2.83g(20mmol)4-氯苯甲胺和7.2g(40mmol)30%浓度的甲醇钠甲醇溶液。在65℃下将混合物搅拌20小时,之后馏出溶剂,残留物用二氯甲烷消化,并将此混合物依次用水、稀盐酸和水洗涤,并经硫酸钠干燥。馏出溶剂后,将残留物用石油醚/乙酸乙酯(10∶1)作洗脱液在硅胶上色谱分离。
得3.4g(理论值的51%)的N-(4-氯苄基)-2-甲氧基亚氨基-2-(4-氯苯基)-乙酰胺,为油状物。1H-NMR(CDCl3,TMS):δ=3.98ppm(s,3H)
类似于实施例1至4,以及根据本发明制备方法的一般性描述,也可以得到例如列于下表7的化合物:
表7
用途实施例实施例A马铃薯晚疫病保护性防治试验溶剂: 4.7份重量的丙酮乳化剂: 0.3份重量的烷芳基聚乙二醇醚
化合物号 | R1 | Z | E/Z-异构体 | R2 | Q | R3 | A | Y | R4 | 物理常数 |
5 | H | Ph | Z | CH3 | O | H | CH(CH3)(R+) | Ph | 4-Cl | log p:369 |
6 | H | Ph | E | CH3 | O | H | CH(CH3)(R+) | Ph | 4-Cl | 熔点:59℃ |
7 | H | Ph | Z | CH3 | O | H | CH2 | Ph | 4-Cl | 熔点:102℃ |
8 | H | Ph | Z | CH3 | O | H | - | Ph | 4-Cl | 熔点:93℃ |
9 | H | Ph | Z | CH3 | O | H | CH(CH3) | Ph | 4-CH3 | 熔点:43℃ |
10 | H | Ph | E | CH3 | O | H | CH2 | Ph | 4-Cl | 熔点:75℃ |
11 | H | Ph | E | CH3 | O | H | CH(CH3) | Ph | 4-CH3 | 熔点:55℃ |
12 | H | Ph | E | CH3 | O | H | - | Ph | 4-Cl | 熔点:194℃ |
13 | H | Ph | E/Z | CH3 | O | H | - | 环己基 | H | 熔点:116℃ |
化合物号 | R1 | Z | E/Z-异构体 | R2 | Q | R3 | A | Y | R4 | 物理常数 |
14 | H | Ph | E/Z | CH3 | O | H | - | 2-吡啶基 | H | 熔点:63℃ |
15 | H | Ph | E/Z | CH3 | O | H | - | 2 6-嘧啶基 | H | log p:1.65 |
16 | H | Ph | E | CH3 | O | H | - | 环己基 | H | 熔点:135℃ |
17 | H | Ph | E/Z | CH3 | O | H | C(CH3)(CN) | Ph | 4-Cl | 熔点:181℃ |
18 | H | Ph | Z | CH3 | O | H | - | 2.6-嘧啶基 | 3,5-(CH3)2 | NMR:3.93(s,3H) |
19 | 4-Cl | Ph | Z | CH3 | O | H | CH(CH3) | Ph | 4-Cl | log p:3.95 |
20 | 4-Cl | Ph | Z | CH3 | O | H | - | 环己基 | H | 熔点:62℃ |
21 | 4-Cl | Ph | E | CH3 | O | H | CH(CH3) | Ph | 4-Cl | log p:3.68 |
22 | 4-Cl | Ph | E | CH3 | O | H | - | 环己基 | H | 熔点:166℃ |
23 | 2,4-(CH3)2 | Ph | E/Z | CH3 | O | H | CH(CH3)(R+) | Ph | 4-Cl | log p:3.95 |
24 | 4-Cl | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2.99 |
25 | H | Ph | E/Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2.27/2.50 |
26 | H | Ph | E | CH3 | O | H | - | 2,6-嘧啶基 | 3,5-(CH3)2 | NMR:4.07(s,3H) |
27 | 2,4-Cl2 | Ph | E/Z | CH3 | O | H | - | 2,6嘧啶基 | 3,5-(CH3)2 | log p:2.46/2.86 |
28 | 2,4-Cl2 | Ph | E/Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.19/3.31 |
29 | 4-Cl | Ph | Z | CH3 | O | H | - | Ph | 4-Cl | 熔点:112℃ |
30 | 2,4-Cl2 | Ph | E/Z | CH3 | O | H | - | Ph | 4-Cl | 熔点:141℃ |
化合物号 | R1 | Z | E/Z-异构体 | R2 | Q | R3 | A | Y | R4 | 物理常数 |
31 | 2,4-Cl2 | Ph | E/Z | CH3 | O | H | CH2 | Ph | 4-Cl | 熔点:109℃ |
32 | 2,4-Cl2 | Ph | E/Z | CH3 | O | H | CH(CH3)(R+) | Ph | 4-Cl | log p:4.02/4.15 |
33 | 2,4-(CH3)2 | Ph | E/Z | CH3 | O | H | - | 环己基 | H | 熔点:72℃ |
34 | 2,4-Cl2 | Ph | E/Z | CH3 | O | H | - | 环己基 | H | 熔点:90℃ |
35 | 2,4-Cl2 | Ph | E/Z | CH3 | O | H | - | Ph | 2-异丙基 | log p:4.32/4.47 |
36 | 2,4-Cl2 | Ph | E/Z | CH3 | O | H | - | Ph | 2-环己基 | 熔点:79℃ |
37 | 2,4-(CH3)2 | Ph | E | CH3 | O | H | - | Ph | 2-仲丁基 | log p:4.65 |
38 | 2,4-(CH3)2 | Ph | Z | CH3 | O | H | - | Ph | 2-仲丁基 | NMR:4.13(s,3H) |
39 | H | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log P:2.50 |
40 | H | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2.26 |
41 | 4-CH3 | Ph | E/Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2.53/2.77 |
42 | 4-CH3 | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | 熔点:72℃ |
43 | 4-CH3 | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 4-F | 熔点:44℃ |
44 | 4-CH3 | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 3-Cl | log p:3.63 |
45 | 4-CH3 | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 3-OCH3 | log p:3.20 |
46 | 4-CH3 | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 2,4-Cl2 | log p:4.15 |
47 | 4-CH3 | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 4-OCH3 | log p:3.16 |
化合物号 | R1 | Z | E/Z-异构体 | R2 | Q | R3 | A | Y | R4 | 物理常数 |
48 | 4-CH3 | Ph | E/Z | CH3 | O | H | - | Ph | 3,4-(OCH3)2 | log p:2.59/2.91 |
49 | 4-CH3 | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 4-F | 熔点:71℃ |
50 | 4-CH3 | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 3-OCH3 | 熔点:94℃ |
51 | 4-CH3 | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 4-OCH3 | 熔点:85℃ |
52 | 4-CH3 | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 2-OCH3 | log p:3.40 |
53 | 4-CH3 | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 3-F | log p:3.20 |
54 | 4-OCH3 | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2.25 |
55 | 4-OCH3 | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2.50 |
56 | 4-CH3 | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 2-Cl | log p:3.64 |
57 | 4-CH3 | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 2,4-Cl2 | 熔点:101℃ |
58 | 4-CH3 | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 3-Cl | 熔点:103℃ |
59 | 4-CH3 | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 4-Cl | 熔点:75℃ |
60 | 4-CH3 | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | H | log p:3.26 |
61 | 4-CH3 | Ph | Z | CH3 | O | CH3 | CH2-CH2 | Ph | H | log p:3.57 |
62 | 4-CH3 | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 2-OCH3 | 熔点:94℃ |
63 | 4-CH3 | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 3-F | 熔点:92℃ |
64 | 4-CH3 | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 2,5-(OCH3)2 | log p:3.75 |
化合物号 | R1 | Z | E/Z-异构体 | R2 | Q | R3 | A | Y | R4 | 物理常数 |
65 | 4-CH3 | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 4-Br | 熔点:44℃ |
66 | 4-CH3 | Ph | E/Z | CH3 | O | H | CH2 | Ph | 3,4-(OCH3)2 | NMR:2.35(s,3H) |
67 | 4-CH3 | Ph | Z | CH3 | O | CH3 | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.03 |
68 | 4-CH3 | Ph | E | CH3 | O | H | CH2-CH2 | Ph | H | 熔点:85℃ |
69 | 4-CH3 | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 2-Cl | 熔点:93℃ |
70 | 4-CH3 | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 4-Cl | 熔点:104℃ |
71 | 4-CH3 | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 4-Br | 熔点:122℃ |
72 | 5-CH3 | 2噻吩基 | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | 熔点:79℃ |
73 | 5-CH3 | 2-噻吩基 | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2.46 |
74 | 4-CH3 | Ph | E | CH3 | O | CH3 | CH2-CH2 | Ph | 3,4-(OCH3)2 | log P:2.86 |
75 | 4-CH3 | Ph | E | CH3 | O | CH3 | CH2-CH2 | Ph | H | log P:3.45 |
76 | 4-CH3 | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 2,5-(OCH3)2 | log p:3.04 |
77 | 4-Cl | Ph | E/Z | C2H5 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.07/3.34 |
78 | 4-OC2H5 | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2.83 |
79 | 4-Cl | Ph | E/Z | H | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | NMR:3.87(s,3H) |
80 | 4-C2H5 | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | NMR:3.95(s,3H) |
81 | 4-C2H5 | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2.86 |
化合物号 | R1 | Z | E/Z-异构体 | R2 | Q | R3 | A | Y | R4 | 物理常数 |
82 | 4-OC2H5 | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2.59 |
83 | 4-CH(CH3)2 | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | NMR:3.88(s,3H) |
84 | 4-CH(CH3)2 | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | NMR:3.81(s,3H) |
85 | 5-CH3 | 2-呋喃基 | E/Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2.04/2.26 |
86 | 4-CH3 | 2-噻吩基 | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2.85 |
87 | 4-CH3 | 2-噻吩基 | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2,54 |
88 | 5-CH3 | 2-呋喃基 | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2.04 |
89 | 5-CH3 | 2-呋喃基 | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2.26 |
90 | 5-OCH3 | 2-噻吩基 | E/Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2.04/2.14 |
91 | 3,4-(CH3)2 | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.00 |
92 | 4-C(CH3)3 | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.72 |
93 | 4-F | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2.61 |
94 | 4-Br | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.08 |
95 | 4-Cl | 2-噻吩基 | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2.56 |
96 | 4-Br | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2.82 |
97 | 5-Cl | 2-噻吩基 | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | 熔点:91℃ |
98 | 4-F | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2.39 |
化合物号 | R1 | Z | E/Z-异构体 | R2 | Q | R3 | A | Y | R4 | 物理常数 |
99 | 3,4-(CH3)2 | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2.75 |
100 | H | 3-吲哚基 | E/Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2.21/2.28 |
101 | 3,4-Cl2 | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.43 |
102 | 4-C(CH3)2 | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.39 |
103 | 5-Cl | 2-噻吩基 | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | 熔点:98℃ |
104 | 4-CH3 | Ph | Z | C2H5 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.13 |
105 | 4-NO2 | Ph | E/Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2.45/2.66 |
106 | 3,4-(OCH3)2 | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2.21 |
107 | 4-Cl | 2-噻吩基 | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | 熔点:88℃ |
108 | 3,4-Cl2 | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | 熔点:122℃ |
109 | 4-SO2CH3 | Ph | E/Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | 熔点:94℃ |
110 | 4-CH3 | Ph | E | C2H5 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2.85 |
11 | H | 2苯并噻吩基 | E/Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2.84/2.91 |
112 | H | 2-萘基 | E/Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | 熔点:64℃ |
113 | 3,4-(OCH3)2 | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | 熔点:122℃ |
114 | 3,4-(CH2)3- | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.01 |
化合物号 | R1 | Z | E/Z-异构体 | R2 | Q | R3 | A | Y | R4 | 物理常数 |
115 | 4-(CH2)2CH3 | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.53 |
116 | 4-C2H5 | Ph | Z | C2H5 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | 熔点:66℃ |
117 | 3,4-(CH2)4- | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.44 |
118 | 4-CH2CH(CH3)2 | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.87 |
119 | 5-Br | 2-噻吩基 | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | 熔点:80℃ |
120 | 4-OPh | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | 熔点:42℃ |
121 | 4-(CH2)2CH3 | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p.3.91 |
122 | 4-C2H5 | Ph | E | C2H5 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | 熔点:82℃ |
123 | 3,4-(CH2)3- | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | 熔点:98℃ |
124 | 4-(CH2)2CH3 | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.25 |
125 | 4-CH2CH(CH3)2 | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.58 |
126 | 4-OCH2Ph | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.49 |
127 | 5-C2H5 | 2噻吩基 | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.22 |
128 | 4-Ph | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.50 |
129 | 4-OPh | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.24 |
130 | 5-Br | 2-噻吩基 | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log P:2.87 |
化合物号 | R1 | Z | E/Z-异构体 | R2 | Q | R3 | A | Y | R4 | 物理常数 | |
131 | 3,4-(CH2)4- | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | 熔点:100℃ | |
132 | 4-(CH2)3CH3 | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.62 | |
133 | 4-OCH2Ph | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | 熔点:123℃ | |
134 | H | 2-噻吩基 | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | 熔点:81℃ | |
135 | 3,4-(C2H5)2 | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.67 | |
136 | 4-Ph | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | 熔点:110℃ | |
137 | 4-SCH3 | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2.86 | |
138 | 4-CH(CH3)C2H5 | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.82 | |
139 | 4-Br | Ph | E/Z | C2H5 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.15/3.43 | |
140 | 3,4-OCH2O- | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2.40 | |
141 | 3,4-O(CH2)2O- | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log P:2.41 | |
142 | 4-SCH3 | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | 熔点:98℃ | |
143 | 5-C2H5 | 2-噻吩基 | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2.77 | |
144 | 3,4-(C2H5)2 | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | 熔点:78℃ | |
145 | 4-CH(CH3)C2H5 | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.52 | |
146 | 4-Br | Ph | E | C2H5 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.15 |
化合物号 | R1 | Z | E/Z-异构体 | R2 | Q | R3 | A | Y | R4 | 物理常数 | |
147 | 3,4-O(CH2)O- | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | 熔点:134℃ | |
148 | 3,4-F2 | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2.59 | |
149 | 3,4-O(CH2)2O | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2.19 | |
150 | 4,5-Br2 | 2噻吩基 | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | 熔点:104℃ | |
151 | 4-(CH2)4CH3 | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:4.34 | |
152 | H | 2-噻吩基 | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | 熔点:92℃ | |
153 | 4-环丙基 | Ph | E/Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | NMR:3.88(s,3H) | |
154 | 45-Br2 | 2-噻吩基 | E/Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | NMR:4.07(s,3H) | |
155 | 4-(CH2)4CH3 | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:4.04 | |
156 | 3,4-F2 | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | 熔点:104℃ | |
157 | 4-环丙基 | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | NMR:3.82(s,3H) | |
158 | 4-F,3-OCH3 | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2.50 | |
159 | H | 1-萘基 | E/Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | 熔点:63℃ | |
160 | 4-F,3-OCH3 | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | 熔点:102℃ | |
161 | 4-OCH3 | Ph | Z | C2H5 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | 熔点:43℃ |
化合物号 | R1 | Z | E/Z-异构体 | R2 | Q | R3 | A | Y | R4 | 物理常数 | |
162 | 4-环已基 | Ph | E/Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:4.03/4.35 | |
163 | 4-(CH2)5CH3 | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:4.78 | |
164 | 4-(CH2)6CH3 | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:5.23 | |
165 | 3,4-(CH2)3- | Ph | Z | C2H5 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.56 | |
166 | 3,4-(CH2)4- | Ph | Z | C2H5 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.84 | |
167 | 4-CH3 | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2.79 | |
168 | 4-OCH3 | Ph | E | C2H5 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | 熔点:86℃ | |
169 | 4-(CH2)5CH3 | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:4.47 | |
170 | 3,4-(CH2)3- | Ph | E | C2H5 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.25 | |
171 | 4-环己基 | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:4.03 | |
172 | 4-(CH2)6CH3 | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:4.92 | |
173 | 3,4-(CH2)4- | Ph | E | C2H5 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.53 | |
174 | 3-Cl | Ph | E/Z | C2H5 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.08/3.30 | |
175 | 4-OCF3 | Ph | E/Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2.75/3.11 | |
176 | 3-OCH3 | Ph | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2.03 | |
177 | 4-CH3 | Ph | E/Z | CH2Ph | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.47/3.69 | |
178 | 4-Br | Ph | E/Z | CH2Ph | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.76/3.99 |
化合物号 | R1 | Z | E/Z-异构体 | R2 | Q | R3 | A | Y | R4 | 物理常数 |
179 | 4-Cl | Ph | E/Z | CH2Ph | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.67/3.89 |
180 | 3,4-(CH2)4- | Ph | E/Z | CH2Ph | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:4.12/4.36 |
181 | 4-CH3 | Ph | E/Z | C(CH3)3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.58/3.79 |
182 | 4-CH3 | Ph | E/Z | (CH2)2CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.20/3.50 |
183 | 4-CH3 | Ph | E/Z | 烯丙基 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2.81/3.01 |
184 | 4-Cl | Ph | Z | (CH2)2CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.75 |
185 | 3,4-(CH2)3- | Ph | E/Z | C(CH3)3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.98/4.19 |
186 | 3,4-(CH2)3- | Ph | E/Z | CH2Ph | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.85/4.06 |
187 | 3-OCH3 | Ph | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2.01 |
188 | 3,4-(CH2)3- | Ph | E/Z | 烯丙基 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.39/3.64 |
189 | 4-CH3 | Ph | E/Z | CH(CH3)2 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.21/3.47 |
190 | 4-Cl | Ph | E/Z | (CH2)3CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.81/4.14 |
191 | 3,4-(CH2)3- | Ph | E/Z | (CH2)3CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:4.00/4.33 |
192 | 4-Cl | Ph | E/Z | 烯丙基 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.22/3.47 |
193 | 3,4-(CH2)3- | Ph | E/Z | (CH2)3CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.62/3.92 |
194 | 3,4-(CH2)3- | Ph | E/Z | CH(CH3)2 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.64/3.89 |
195 | 4-C2H5 | Ph | E/Z | CH2PH | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3.83/4.05 |
化合物号 | R1 | Z | E/Z-异构体 | R2 | Q | R3 | A | Y | R4 | 物理常数 |
196 | 3,4-(CH2)4- | Ph | E/Z | H | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2.53/2.68 |
197 | 4-Br | Ph | E/Z | H | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2,32/2,38 |
198 | 3,4-(CH2)3 | Ph | E/Z | 炔丙基 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | NMR:3,86(s,3H) |
199 | 4-C2H5 | Ph | E/Z | H | O | H | CH2-CH2 | Ph | 3,4-(OCH3) | 熔点:122℃ |
200 | 3,4-(CH2)3 | Ph | E/Z | H | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | 熔点:115℃ |
201 | 4-CH3 | Ph | E/Z | H | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | 熔点:143℃ |
202 | 3-CF3 | Ph | E/Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2,99/3,21 |
203 | 3,4-(CH2)3 | Ph | E/Z | CH2CN | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | NMR:3,87(s,3H) |
204 | 4-CF3 | Ph | E/Z | C2H5 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3,32/3,58 |
205 | 4-CF3 | Ph | E/Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3,01/3,25 |
206 | 3-F | Ph | E/Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2,44/2,64 |
207 | H | 2-苯并噻吩基 | E/Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | NMR:3,85(s,3H) |
208 | H | 2-苯并噻吩基 | E/Z | C2H5 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3,24/3,72 |
209 | 3-CH3 | Ph | E/Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2,56/2,76 |
210 | 3-CH3 | Ph | E/Z | C2H5 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2,87/31,0 |
211 | 3-Br | Ph | E/Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2,83/3,05 |
化合物号 | R1 | Z | E/Z-异构体 | R2 | Q | R3 | A | Y | R4 | 物理常数 |
212 | 3-Br | Ph | E/Z | C2H5 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3,18/3,40 |
213 | H | 2苯并噻吩基 | E | C2H5 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | NMR:3,88(s,3H) |
214 | 3,4-(CH2)4 | Ph | E/Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3,17/3,40 |
215 | H | 2-萘基 | E/Z | C2H5 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3,20/3,44 |
216 | H | 2-萘基 | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3) | log p:3,10 |
217 | H | 2-萘基 | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2,87 |
218 | 4,5-Cl2 | 2-噻唑基 | E/Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2,93/2,95 |
219 | 4,5-Cl2 | 2-噻唑基 | E/Z | C2H5 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3,28/3,30 |
220 | 4,5-Cl2 | 2-噻唑基 | Z | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:2,93 |
221 | 4,5-Cl2 | 2-噻唑基 | E | CH3 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | Fp:74℃ |
222 | 4,5-Cl2 | 2-噻唑基 | E | C2H5 | O | H | CH2-CH2 | Ph | 3,4-(OCH3)2 | log p:3,28 |
223 | 4,5-Cl2 | 2-噻唑基 | E | C2H5 | O | H | CH2CH2 | Ph | 3,4-(OCH3)2 | Fp:71℃ |
制备活性化合物的合适制剂时,将1份重量的活性化合物与所述量的溶剂和乳化剂混合,并将该乳油用水稀释至所需浓度。
测试保护性活性时,将幼株用活性化合物制剂喷雾。喷液层变干后,将植株用蔓延疫霉(Phytophthora infestans)的孢子水悬浮液接种。
之后,将植物放置于20℃和100%相对湿度的培养箱中。
接种3天后进行评价。
在此试验中,在喷雾液中活性化合物浓度为100ppm的情况下,显示大于80%作用程度的有本发明化合物24、41和42。实施例B葡萄霜霉病保护性防治试验溶剂: 4.7份重量的丙酮乳化剂: 0.3份重量的烷芳基聚乙二醇醚
制备活性化合物的合适制剂时,将1份重量的活性化合物与所述量的溶剂和乳化剂混合,并将该乳油用水稀释至所需浓度。
测试保护性活性时,将幼株用活性化合物制剂喷雾。喷液层变干后,将植株用葡萄霜霉病菌(Plasmopara viticola)的孢子水悬浮液接种。之后,将植株放在20-22℃和100%相对湿度的培养箱中1天。接着将植物放置于21℃和约90%相对湿度的温室中5天。再将植物在培养箱中湿润和放置1天。
接种6天后进行评价。
在此试验中,在喷雾液中活性化合物浓度为100ppm的情况下,显示大于80%作用程度的有本发明化合物2、24、41、42、73、77、81、82、91、96、98、99、103、110、114、117、122、123、124、126、127、131、132、136、142、143、144、146、147、170、171和173。
Claims (10)
1.式(I)化合物,其中A 代表单键或任选取代的亚烷基,Q 代表氧或硫,R1 代表各任选取代的环烷基、环烯基、芳基或杂环基,R2和R3相同或不同且各代表氢或各任选取代的烷基、链烯基、炔基或
环烷基,和R4 代表各任选取代的环烷基、环烯基、芳基或杂环基。
2.根据权利要求1的式(I)化合物,其中A 代表单键,或代表具有1至6个碳原子的亚烷基,它任选由相同或
不同的取代基单或多取代,可能的取代基优选选自下列:
卤素、氰基、硝基、氨基、羟基、甲酰基、羧基、氨基甲酰基或硫
代氨基甲酰基;
直链或支链烷氧基、烷硫基、烷基亚磺酰基或烷基磺酰基,它们各
具有1至6个碳原子;
直链或支链链烯基或链烯氧基,它们各具有2至6个碳原子;
直链或支链卤代烷氧基、卤代烷硫基、卤代烷基亚磺酰基或卤代烷
基磺酰基,它们各具有1至6个碳原子和1至13个相同或不同的卤
原子;
直链或支链卤代链烯基或卤代链烯氧基,它们各具有2至6个碳原
子和1至13个相同或不同的卤原子;
直链或支链烷基氨基、二烷基氨基、烷基羰基、烷基羰氧基、烷氧
基羰基、烷基磺酰氧基、肟基烷基或烷氧基亚氨基烷基,它们各在
其每一烷基部分具有1至6个碳原子;
具有3至6个碳原子的环烷基;
和取代的芳基或杂环基,它们各任选以相同或不同的方式由下列取
代基单或多取代:
卤素、氰基和/或具有1至4个碳原子的直链或支链烷基,
和/或具有1至4个碳原子和1至9个相同或不同卤原子的直链或支
链卤代烷基,
和/或具有1至4个碳原子的直链或支链烷氧基或烷硫基,
和/或具有1至4个碳原子和1至9个相同或不同卤原子的直链或支
链卤代烷氧基或卤代烷硫基,
和/或二价亚烷基或亚烷二氧基,它们各具有1至6个碳原子且任选
以相同或不同的方式由下列基团单或多取代:卤素和/或具有1至4
个碳原子的直链或支链烷基和/或具有1至4个碳原子和1至9个相
同或不同卤原子的直链或支链卤代烷基,Q 代表氧或硫,R1 代表芳基、具有3至7个碳原子的环烷基或环烯基或具有3
至12个环原子的杂环基,它们各任选由相同或不同的取代基单或
多取代,可能的取代基优选选自下列:
卤素、氰基、硝基、氨基、羟基、甲酰基、羧基、氨基甲酰基或硫
代氨基甲酰基;
直链或支链烷基、烷氧基、烷硫基、烷基亚磺酰基或烷基磺酰基,
它们各具有1至8个碳原子;
直链或支链链烯基或链烯氧基,它们各具有2至6个碳原子;
直链或支链卤代烷基、卤代烷氧基、卤代烷硫基、卤代烷基亚磺酰
基或卤代烷基磺酰基,它们各具有1至6个碳原子和1至13个相同
或不同的卤原子;
直链或支链卤代链烯基或卤代链烯氧基,它们各具有2至6个碳原
子和1至13个相同或不同的卤原子;
直链或支链烷基氨基、二烷基氨基、烷基羰基、烷基羰氧基、烷氧
基羰基、烷基磺酰氧基、肟基烷基或烷氧基亚氨基烷基,它们各在
其每一烷基部分具有1至8个碳原子;
二价亚烷基或亚烷二氧基,它们各具有1至6个碳原子且任选以相
同或不同的方式由下列基团单或多取代:卤素和/或具有1至4个碳
原子的直链或支链烷基和/或具有1至4个碳原子和1至9个相同或
不同卤原子的直链或支链卤代烷基,
具有3至6个碳原子的环烷基;
和取代的芳基、芳氧基、芳硫基、芳烷基、芳基烷氧基、芳基烷硫
基、杂环基、杂环基氧基、杂环基硫基、杂环基烷基、杂环基烷氧
基或杂环基烷硫基,它们各任选以相同或不同的方式由下列基团单
或多取代:
卤素、氰基和/或具有1至4个碳原子的直链或支链烷基,
和/或具有1至4个碳原子和1至9个相同或不同卤原子的直链或支
链卤代烷基,
和/或具有1至4个碳原子的直链或支链烷氧基或烷硫基,
和/或具有1至4个碳原子和1至9个相同或不同卤原子的直链或支
链卤代烷氧基或卤代烷硫基,
和/或二价亚烷基或亚烷二氧基,它们各具有1至6个碳原子且任选
以相同或不同的方式由下列基团单或多取代:卤素和/或具有1至4
个碳原子的直链或支链烷基和/或具有1至4个碳原子和1至9个相
同或不同卤原子的直链或支链卤代烷基,R2 代表氢,或代表具有1至4个碳原子的烷基,各具有2至4个碳原
子的链烯基或炔基或具有3至6个碳原子的环烷基,它们各任选以
相同或不同的方式由下列基团单或多取代:卤素、氰基、羟基、氨
基、C1-C4-烷氧基、C1-C4-烷硫基、C1-C4-烷基亚磺酰基或C1-
C4-烷基磺酰基(它们各任选由卤素取代)或由任选取代的苯基取
代,R3 代表氢或代表具有1至4个碳原子的烷基,R4 代表芳基、具有3至8个碳原子的环烷基或环烯基或具有3至12
个环原子的杂环基,它们各任选由相同或不同的取代基单或多取
代,可能的取代基优选选自下列:
卤素、氰基、硝基、氨基、羟基、甲酰基、羧基、氨基甲酰基或硫
代氨基甲酰基;
直链或支链烷基、烷氧基、烷硫基、烷基亚磺酰基或烷基磺酰基,
它们各具有1至6个碳原子;
直链或支链链烯基或链烯氧基,它们各具有2至6个碳原子;
直链或支链卤代烷基、卤代烷氧基、卤代烷硫基、卤代烷基亚磺酰
基或卤代烷基磺酰基,它们各具有1至6个碳原子和1至13个相同
或不同的卤原子;
直链或支链卤代链烯基或卤代链烯氧基,它们各具有2至6个碳原
子和1至13个相同或不同的卤原子;
直链或支链烷基氨基、二烷基氨基、烷基羰基、烷基羰氧基、烷氧
基羰基、烷基磺酰氧基、肟基烷基或烷氧基亚氨基烷基,它们各在
其每一烷基部分具有1至6个碳原子;
二价亚烷基或亚烷二氧基,它们各具有1至6个碳原子且任选以相
同或不同的方式由下列基团单或多取代:卤素和/或具有1至4个碳
原子的直链或支链烷基和/或具有1至4个碳原子和1至9个相同或
不同卤原子的直链或支链卤代烷基,
具有3至6个碳原子的环烷基;
和取代的芳基、芳氧基、芳硫基、芳烷基、芳基烷氧基、芳基烷硫
基、杂环基、杂环基氧基、杂环基硫基、杂环基烷基、杂环基烷氧
基或杂环基烷硫基,它们各任选以相同或不同的方式由下列基团取
代基单或多取代:
卤素、氰基和/或具有1至4个碳原子的直链或支链烷基,
和/或具有1至4个碳原子和1至9个相同或不同的卤原子的直链或
支链卤代烷基,
和/或具有1至4个碳原子的直链或支链烷氧基或烷硫基,
和/或具有1至4个碳原子和1至9个相同或不同卤原子的直链或支
链卤代烷氧基或卤代烷硫基,
和/或二价亚烷基或亚烷二氧基,它们各具有1至6个碳原子且任选
以相同或不同的方式由下列基团单或多取代:卤素和/或具有1至4
个碳原子的直链或支链烷基和/或具有1至4个碳原子和1至9个相
同或不同的卤原子的直链或支链卤代烷基。
3.根据权利要求1的式(I)化合物,其中A 代表单键,或代表亚甲基、1,1-亚乙基、1,2-亚乙基、1,1-、
1,2-、1,3-或2,2-亚丙基、1,1-、1,2-、1,3-、1,4-、2,2-、2,3-亚丁
基或1,1-、1,2-或1,3-(2-甲基亚丙基),它门任选以相同或不同
的方式由下列基团单或多取代:氟、氯、氰基或甲氧基,Q 代表氧或硫,R1 代表环丙基、环丁基、环戊基或环己基、苯基、萘基、呋喃基、苯
并呋喃基、吡咯基、吲哚基、噻吩基、苯并噻吩基、噁唑基、异噁
唑基、噻唑基、异噻唑基、噁二唑基、噻二唑基、吡啶基、喹啉基、
嘧啶基、哒嗪基、吡嗪基、环氧乙烷基、氧杂环丁烷基、四氢呋喃
基、全氢吡喃基、吡咯烷基、哌啶基或吗啉基,它们各任选被单至
三取代,可能的取代基优选选自下列:
氟、氯、溴、氰基、硝基、氨基、羟基、甲酰基、羧基、氨基甲酰
基、硫代氨基甲酰基、甲基、乙基、正-或异-丙基、正-、异-、仲-
或叔-丁基、正戊基、正己基、正庚基、甲氧基、乙氧基、正或异丙
氧基、甲硫基、乙硫基、正-或异-丙硫基、甲基亚磺酰基、乙基亚磺
酰基、甲磺酰基或乙磺酰基、三氟甲基、三氟乙基、二氟甲氧基、
三氟甲氧基、二氟氯甲氧基、三氟乙氧基、二氟甲硫基、二氟氯甲
硫基、三氟甲硫基、三氟甲基亚磺酰基或三氟甲磺酰基、甲氨基、
乙氨基、正-或异-丙氨基、二甲氨基、二乙氨基、乙酰基、丙酰基、
乙酰氧基、甲氧羰基、乙氧羰基、甲基磺酰氧基、乙基磺酰氧基、
肟基甲基、肟基乙基、甲氧基亚氨基甲基、乙氧基亚氨基甲基、甲
氧基亚氨基乙基或乙氧基亚氨基乙基;
二价三亚甲基(丙-1,3-二基)、四亚甲基(丁-1,4-二基)、亚甲
二氧基或亚乙二氧基,它们各任选以相同或不同的方式由下列基团
单或多取代:氟、氯、甲基、三氟甲基、乙基或正-或异-丙基;
环丙基、环丁基、环戊基或环己基;
苯基、苄基、苯氧基和苄氧基,它们任选由上面提及的取代基取代;R2 代表氢,或代表甲基、乙基、正-或异-丙基、或正-、异-、仲-或叔-
丁基,或代表苄基或炔丙基或烯丙基,R3 代表氢,或代表甲基或乙基,R4 代表环丙基、环丁基、环戊基或环己基、苯基、萘基、呋喃基、苯
并呋喃基、吡咯基、吲哚基、噻吩基、苯并噻吩基、噁唑基、异噁
唑基、噻唑基、异噻唑基、噁二唑基、噻二唑基、吡啶基、喹啉基、
嘧啶基、哒嗪基、吡嗪基、环氧乙烷基、氧杂环丁烷基、四氢呋喃
基、全氢吡喃基、吡咯烷基、哌啶基或吗啉基,它们各任选被单至
三取代,可能的取代基优选选自下列:
氟、氯、溴、氰基、硝基、氨基、羟基、甲酰基、羧基、氨基甲酰
基、硫代氨基甲酰基、甲基、乙基、正-或异-丙基、正-、异-、仲-
或叔-丁基、甲氧基、乙氧基、正-或异-丙氧基、甲硫基、乙硫基、
正-或异-丙硫基、甲基亚磺酰基、乙基亚磺酰基、甲磺酰基或乙磺酰
基、三氟甲基、三氟乙基、二氟甲氧基、三氟甲氧基、二氟氯甲氧
基、三氟乙氧基、二氟甲硫基、二氟氯甲硫基、三氟甲硫基、三氟
甲基亚磺酰基或三氟甲磺酰基、甲氨基、乙氨基、正-或异-丙氨基、
二甲氨基、二乙氨基、乙酰基、丙酰基、乙酰氧基、甲氧羰基、乙
氧羰基、甲基磺酰氧基、乙基磺酰氧基、肟基甲基、肟基乙基、甲
氧基亚氨基甲基、乙氧基亚氨基甲基、甲氧基亚氨基乙基或乙氧基
亚氨基乙基;
二价三亚甲基(丙-1,3-二基)、四亚甲基(丁-1,4-二基)、亚甲
二氧基或亚乙二氧基,它们各任选以相同或不同的方式由下列基团
单或多取代:氟、氯、甲基、三氟甲基、乙基或正-或异-丙基;
环丙基、环丁基、环戊基或环己基。
4.根据权利要求1的式(I)化合物,其中A 代表单键,或代表亚甲基、1,1-亚乙基、1,2-亚乙基、1,1-、
1,2-、1,3-或2,2-亚丙基、1,1-、1,2-、1,3-、1,4-、2,2-、2,3-亚
丁基或1,1-、1,2-或1,3-(2-甲基亚丙基),它们任选以相同或不
同的方式由下列基团单或多取代:氟、氯、氰基或甲氧基,
Q 代表氧或硫,R1 代表环丁基、环戊基或环己基,它们各任选被单至六取代,优选的
取代基是下文提及的那些取代基;
或代表苯基、萘基、呋喃基、苯并呋喃基、噻吩基、苯并噻吩基、
吡啶基、喹啉基、四氢呋喃基或全氢吡喃基,它们各任选被单至三
取代,可能的取代基优选选自下列:
氟、氯、溴、氰基、硝基、甲基、乙基、正-或异-丙基、正-、异-、
仲-或叔-丁基、正戊基、正己基、正庚基、甲氧基、乙氧基、正-或
异-丙氧基、甲硫基、乙硫基、正-或异-丙硫基、甲基亚磺酰基、乙
基亚磺酰基、甲磺酰基或乙磺酰基、三氟甲基、三氟乙基、二氟甲
氧基、三氟甲氧基、二氟氯甲氧基、三氟乙氧基、二氟甲硫基、二
氟氯甲硫基、三氟甲硫基、三氟甲基亚磺酰基、三氟甲磺酰基、乙
酰基、丙酰基、乙酰氧基、甲氧羰基、乙氧羰基、甲基磺酰氧基、
乙基磺酰氧基、肟基甲基、肟基乙基、甲氧基亚氨基甲基、乙氧基
亚氨基甲基、甲氧基亚氨基乙基或乙氧基亚氨基乙基;
二价三亚甲基(丙-1,3-二基)、四亚甲基(丁-1,4-二基)、亚甲
二氧基或亚乙二氧基,它们各任选以相同或不同的方式由下列基团
单或多取代:氟、氯、甲基、三氟甲基、乙基或正-或异-丙基;
环丙基、环戊基或环己基;
苯基、苯氧基和苄氧基,它们任选由上文提及的取代基取代;R2 代表氢、甲基、乙基、正-或异-丙基、或正-、异-、仲-或叔-丁基,
代表苄基或烯丙基,R3 代表氢或甲基,R4 代表环丙基、环丁基、环戊基或环己基,它们各任选被单至六取代,
优选的取代基是下文提及的那些取代基;
或代表苯基、萘基、呋喃基、苯并呋喃基、吡咯基、吲哚基、噻吩
基、苯并噻吩基、噁唑基、异噁唑基、噻唑基、异噻唑基、噁二唑
基、噻二唑基、吡啶基、喹啉基、嘧啶基、哒嗪基、吡嗪基、环氧
乙烷基、氧杂环丁烷基、四氢呋喃基、全氢吡喃基、吡咯烷基、哌
啶基或吗啉基,它们各任选被单至三取代,可能的取代基优选选自
下列:
氟、氯、溴、氰基、硝基、氨基、羟基、甲酰基、羧基、氨基甲酰
基、硫代氨基甲酰基、甲基、乙基、正-或异-丙基、正-、异-、仲-
或叔-丁基、甲氧基、乙氧基、正-或异-丙氧基、甲硫基、乙硫基、
正-或异-丙硫基、甲基亚磺酰基、乙基亚磺酰基、甲磺酰基或乙磺酰
基、三氟甲基、三氟乙基、二氟甲氧基、三氟甲氧基、二氟氯甲氧
基、三氟乙氧基、二氟甲硫基、二氟氯甲硫基、三氟甲硫基、三氟
甲基亚磺酰基或三氟甲磺酰基、甲氨基、乙氨基、正-或异-丙氨
基、二甲氨基、二乙氨基、乙酰基、丙酰基、乙酰氧基、甲氧羰基、
乙氧羰基、甲基磺酰氧基、乙基磺酰氧基、肟基甲基、肟基乙基、
甲氧基亚氨基甲基、乙氧基亚氨基甲基、甲氧基亚氨基乙基或乙氧
基亚氨基乙基;
二价三亚甲基(丙-1,3-二基)、四亚甲基(丁-1,4-二基)、亚甲
二氧基或亚乙二氧基,它们各任选以相同或不同的方式由下列基团
单或多取代:氟、氯、甲基、三氟甲基、乙基或正-或异-丙基;
环丙基、环丁基、环戊基或环己基。
5.根据权利要求1的式(I)化合物,其中A 代表单键,或代表亚甲基、1,1-亚乙基、1,2-亚乙基、1,1-亚丙基、
1,2-亚丙基、1,3-亚丙基或2,2-亚丙基,Q 代表氧,R1 代表苯基、噻吩基或呋喃基,它们任选由下列基团单或二取代:溴、
氯、氟、硝基、甲磺酰基、苯基、苯氧基、苄氧基、环丙基、环己
基、甲基、乙基、正-或异-丙基、正-、异-、仲-或叔-丁基、正戊基、
正己基、正庚基、甲氧基、乙氧基、三氟甲基、三氟甲氧基和/或甲
硫基,
或代表苯基,该苯基由各任选被氟取代的3,4-亚甲基-和亚乙二氧
基、丙-1,3-二基或丁-1,4-二基取代,
或代表萘基、苯并呋喃基或苯并噻吩基,R2 代表氢、甲基或乙基,或代表正-或异-丙基,或代表正-、异-、仲-
或叔-丁基,或代表苄基或烯丙基,R3 代表氢或甲基,R4 代表环己基或任选单至三取代的苯基、噻吩基、呋喃基、苯并呋喃
基、苯并噻吩基、吡啶基、嘧啶基、萘基或喹啉基,可能的取代基
优选选自下列:
氟、氯、溴、氰基、硝基、氨基、羟基、甲酰基、羧基、氨基甲酰
基、硫代氨基甲酰基、甲基、乙基、正-或异-丙基、正-、异-、仲-
或叔-丁基、甲氧基、乙氧基、正-或异-丙氧基、甲硫基、乙硫基、
正或异丙硫基、甲基亚磺酰基、乙基亚磺酰基、甲磺酰基或乙磺酰
基、三氟甲基、三氟乙基、二氟甲氧基、三氟甲氧基、二氟氯甲氧
基、三氟乙氧基、二氟甲硫基、二氟氯甲硫基、三氟甲硫基、三氟
甲基亚磺酰基或三氟甲磺酰基、甲氨基、乙氨基、正-或异-丙氨
基、二甲氨基、二乙氨基、乙酰基、丙酰基、乙酰氧基、甲氧羰基、
乙氧羰基、甲基磺酰氧基、乙基磺酰氧基、肟基甲基、肟基乙基、
甲氧基亚氨基甲基、乙氧基亚氨基甲基、甲氧基亚氨基乙基或乙氧
基亚氨基乙基;
二价三亚甲基(丙-1,3-二基)、四亚甲基(丁-1,4-二基)、亚甲
二氧基或亚乙二氧基,它们各任选以相同或不同的方式由下列基团
单或多取代:氟、氯、甲基、三氟甲基、乙基或正-或异-丙基。
6.有害生物的防治剂,其特征在于含有至少一种权利要求1的式(I)化合物。
7.防治有害生物的方法,其特征在于,使权利要求1的式(I)化合物作用于有害生物和/或其栖息地。
8.权利要求1至5的式(I)化合物防治有害生物的应用。
9.制备有害生物防治剂的方法,其特征在于,将权利要求1至5的式(I)化合物与填充剂和/或表面活性剂混合。
Applications Claiming Priority (11)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19502813 | 1995-01-30 | ||
DE19502813.9 | 1995-01-30 | ||
DE19503162.8 | 1995-02-01 | ||
DE19503162 | 1995-02-01 | ||
DE19510770.5 | 1995-03-24 | ||
DE19510770 | 1995-03-24 | ||
DE19527099 | 1995-07-25 | ||
DE19527099.1 | 1995-07-25 | ||
DE195431995. | 1995-11-20 | ||
DE19543199A DE19543199A1 (de) | 1995-07-25 | 1995-11-20 | Alkoximinoessigsäureamide |
DE19543199.5 | 1995-11-20 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1169716A true CN1169716A (zh) | 1998-01-07 |
CN1082945C CN1082945C (zh) | 2002-04-17 |
Family
ID=27512441
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN96191663A Expired - Fee Related CN1082945C (zh) | 1995-01-30 | 1996-01-17 | 烷氧基亚氨基乙酰胺 |
Country Status (16)
Country | Link |
---|---|
US (2) | US6130251A (zh) |
EP (1) | EP0807102B1 (zh) |
JP (1) | JPH11500713A (zh) |
CN (1) | CN1082945C (zh) |
AU (1) | AU4536996A (zh) |
BR (1) | BR9606814A (zh) |
CA (1) | CA2211832A1 (zh) |
CZ (1) | CZ294631B6 (zh) |
DE (1) | DE59608263D1 (zh) |
ES (1) | ES2167540T3 (zh) |
HU (1) | HUP9800087A3 (zh) |
MX (1) | MX9705726A (zh) |
PL (1) | PL183585B1 (zh) |
PT (1) | PT807102E (zh) |
SK (1) | SK282830B6 (zh) |
WO (1) | WO1996023763A1 (zh) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101218237B (zh) * | 2005-07-11 | 2012-03-28 | 田边三菱制药株式会社 | 肟衍生物及其制备方法 |
Families Citing this family (19)
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DE59707658D1 (de) | 1996-07-22 | 2002-08-08 | Bayer Ag | Glyoxylsäure-derivate |
DE19648009A1 (de) | 1996-11-20 | 1998-05-28 | Bayer Ag | Glyoxylsäureamide |
EP0862867A3 (de) * | 1997-03-07 | 1999-04-28 | Akzo Nobel N.V. | Wasserdichter Schuh mit Brandsohle und Futtersohle |
DE19726201A1 (de) * | 1997-06-20 | 1998-12-24 | Bayer Ag | Glyoxylsäureamide |
TW564244B (en) | 1999-01-11 | 2003-12-01 | Novartis Ag | Novel propargylether derivatives |
GB9900963D0 (en) * | 1999-01-15 | 1999-03-10 | Novartis Ag | Organic compounds |
EP1200393B1 (en) | 1999-08-13 | 2003-12-10 | Monsanto Technology LLC | Oxime amides and hydrazone amides having fungicidal activity |
DE19958165A1 (de) | 1999-12-02 | 2001-06-07 | Bayer Ag | Glyoxylsäureamide |
TR200201544T2 (tr) * | 1999-12-13 | 2002-11-21 | Bayer Aktiengesellschaft | Fungusid aktivitesine sahip bileşik kombinasyonları. |
DE10019758A1 (de) | 2000-04-20 | 2001-10-25 | Bayer Ag | Fungizide Wirkstoffkombinationen |
CN100475034C (zh) | 2000-06-14 | 2009-04-08 | 巴斯福股份公司 | 苯乙基丙烯酰胺的用途,新的苯乙基丙烯酰胺,其制备及包含它们的组合物 |
AU2003214116A1 (en) * | 2002-03-14 | 2003-09-22 | Basf Aktiengesellschaft | Z-substituted acrylamides, methods for production thereof and agents comprising the same |
WO2003082822A1 (de) * | 2002-03-28 | 2003-10-09 | Basf Aktiengesellschaft | Phenethylacrylamide, verfahren zu deren herstellung sowie sie enthaltende mittel |
US20060041144A1 (en) * | 2002-08-19 | 2006-02-23 | Takashi Komori | Phenylpyridine compound and fungicidal compostion containing the same |
WO2004083193A1 (ja) * | 2003-03-17 | 2004-09-30 | Sumitomo Chemical Company, Limited | アミド化合物およびこれを含有する殺菌剤組成物 |
US7902248B2 (en) | 2006-12-14 | 2011-03-08 | Hoffmann-La Roche Inc. | Oxime glucokinase activators |
WO2008084873A1 (ja) * | 2007-01-10 | 2008-07-17 | Mitsubishi Tanabe Pharma Corporation | オキシム誘導体 |
JP2008019241A (ja) * | 2007-03-01 | 2008-01-31 | Mitsubishi Tanabe Pharma Corp | オキシム誘導体及びその製法 |
CN105503642B (zh) * | 2015-12-17 | 2017-09-15 | 湖南科技大学 | N‑取代‑2‑(2‑羟基苄基)氨基乙酰胺类化合物及其制备和用途 |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH02200658A (ja) * | 1989-01-28 | 1990-08-08 | Kumiai Chem Ind Co Ltd | N―(置換)ベンジルカルボン酸アミド誘導体及び除草剤 |
DE3906160A1 (de) * | 1989-02-28 | 1990-10-11 | Basf Ag | Ortho-substituierte 1-naphthylether und diese enthaltende fungizide |
US5206266A (en) * | 1989-03-09 | 1993-04-27 | Basf Aktiengesellschaft | Substituted oxime ethers and fungicides which contain these compounds |
JP3188286B2 (ja) * | 1991-08-20 | 2001-07-16 | 塩野義製薬株式会社 | フェニルメトキシイミノ化合物およびそれを用いる農業用殺菌剤 |
IL107690A (en) * | 1992-12-14 | 1997-09-30 | Basf Ag | 2, a-DISUBSTITUTED BENZENEACETOTHIOAMIDES, THEIR PREPARATION AND THEIR USE AS PESTICIDES AND FUNGICIDES |
TW299310B (zh) * | 1993-05-18 | 1997-03-01 | Ciba Geigy Ag |
-
1996
- 1996-01-17 MX MX9705726A patent/MX9705726A/es not_active IP Right Cessation
- 1996-01-17 BR BR9606814A patent/BR9606814A/pt not_active Application Discontinuation
- 1996-01-17 SK SK1017-97A patent/SK282830B6/sk unknown
- 1996-01-17 PL PL96321637A patent/PL183585B1/pl not_active IP Right Cessation
- 1996-01-17 JP JP8523202A patent/JPH11500713A/ja not_active Ceased
- 1996-01-17 WO PCT/EP1996/000179 patent/WO1996023763A1/de active IP Right Grant
- 1996-01-17 AU AU45369/96A patent/AU4536996A/en not_active Abandoned
- 1996-01-17 ES ES96901289T patent/ES2167540T3/es not_active Expired - Lifetime
- 1996-01-17 US US08/875,300 patent/US6130251A/en not_active Expired - Fee Related
- 1996-01-17 CN CN96191663A patent/CN1082945C/zh not_active Expired - Fee Related
- 1996-01-17 CA CA002211832A patent/CA2211832A1/en not_active Abandoned
- 1996-01-17 DE DE59608263T patent/DE59608263D1/de not_active Expired - Fee Related
- 1996-01-17 PT PT96901289T patent/PT807102E/pt unknown
- 1996-01-17 EP EP96901289A patent/EP0807102B1/de not_active Expired - Lifetime
- 1996-01-17 HU HU9800087A patent/HUP9800087A3/hu unknown
- 1996-01-17 CZ CZ19972353A patent/CZ294631B6/cs not_active IP Right Cessation
-
2000
- 2000-06-30 US US09/608,864 patent/US6730705B1/en not_active Expired - Fee Related
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101218237B (zh) * | 2005-07-11 | 2012-03-28 | 田边三菱制药株式会社 | 肟衍生物及其制备方法 |
Also Published As
Publication number | Publication date |
---|---|
PL183585B1 (pl) | 2002-06-28 |
ES2167540T3 (es) | 2002-05-16 |
AU4536996A (en) | 1996-08-21 |
HUP9800087A3 (en) | 1999-03-29 |
CZ235397A3 (en) | 1997-10-15 |
EP0807102B1 (de) | 2001-11-21 |
PT807102E (pt) | 2002-05-31 |
DE59608263D1 (de) | 2002-01-03 |
HUP9800087A2 (hu) | 1998-04-28 |
MX9705726A (es) | 1997-11-29 |
CZ294631B6 (cs) | 2005-02-16 |
EP0807102A1 (de) | 1997-11-19 |
US6130251A (en) | 2000-10-10 |
CA2211832A1 (en) | 1996-08-08 |
US6730705B1 (en) | 2004-05-04 |
CN1082945C (zh) | 2002-04-17 |
BR9606814A (pt) | 1997-12-30 |
PL321637A1 (en) | 1997-12-22 |
SK101797A3 (en) | 1997-11-05 |
SK282830B6 (sk) | 2002-12-03 |
JPH11500713A (ja) | 1999-01-19 |
WO1996023763A1 (de) | 1996-08-08 |
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