JP4165808B2 - フタル酸ジアミド、該生成物の製造方法及び害虫を駆除するためのその使用 - Google Patents
フタル酸ジアミド、該生成物の製造方法及び害虫を駆除するためのその使用 Download PDFInfo
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- JP4165808B2 JP4165808B2 JP2002563159A JP2002563159A JP4165808B2 JP 4165808 B2 JP4165808 B2 JP 4165808B2 JP 2002563159 A JP2002563159 A JP 2002563159A JP 2002563159 A JP2002563159 A JP 2002563159A JP 4165808 B2 JP4165808 B2 JP 4165808B2
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- YFGYUFNIOHWBOB-UHFFFAOYSA-N pirimicarb Chemical compound CN(C)C(=O)OC1=NC(N(C)C)=NC(C)=C1C YFGYUFNIOHWBOB-UHFFFAOYSA-N 0.000 description 1
- 238000003976 plant breeding Methods 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000011120 plywood Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920002432 poly(vinyl methyl ether) polymer Polymers 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- JPFWJDMDPLEUBD-ITJAGOAWSA-N polyoxorim Polymers O[C@@H]1[C@H](O)[C@@H]([C@H](NC(=O)[C@H]([C@H](O)[C@@H](O)COC(N)=O)N)C(O)=O)O[C@H]1N1C(=O)NC(=O)C(C(O)=O)=C1 JPFWJDMDPLEUBD-ITJAGOAWSA-N 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000005077 polysulfide Substances 0.000 description 1
- 229920001021 polysulfide Polymers 0.000 description 1
- 150000008117 polysulfides Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920006215 polyvinyl ketone Polymers 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 244000144977 poultry Species 0.000 description 1
- 235000013594 poultry meat Nutrition 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- TVLSRXXIMLFWEO-UHFFFAOYSA-N prochloraz Chemical compound C1=CN=CN1C(=O)N(CCC)CCOC1=C(Cl)C=C(Cl)C=C1Cl TVLSRXXIMLFWEO-UHFFFAOYSA-N 0.000 description 1
- QYMMJNLHFKGANY-UHFFFAOYSA-N profenofos Chemical compound CCCSP(=O)(OCC)OC1=CC=C(Br)C=C1Cl QYMMJNLHFKGANY-UHFFFAOYSA-N 0.000 description 1
- WHMZYGMQWIBNOC-UHFFFAOYSA-N propan-2-yl n-(3,4-dimethoxyphenyl)carbamate Chemical compound COC1=CC=C(NC(=O)OC(C)C)C=C1OC WHMZYGMQWIBNOC-UHFFFAOYSA-N 0.000 description 1
- FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000011814 protection agent Substances 0.000 description 1
- 239000003531 protein hydrolysate Substances 0.000 description 1
- 210000001938 protoplast Anatomy 0.000 description 1
- 239000013225 prussian blue Substances 0.000 description 1
- 229960003351 prussian blue Drugs 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- QHMTXANCGGJZRX-WUXMJOGZSA-N pymetrozine Chemical compound C1C(C)=NNC(=O)N1\N=C\C1=CC=CN=C1 QHMTXANCGGJZRX-WUXMJOGZSA-N 0.000 description 1
- QHGVXILFMXYDRS-UHFFFAOYSA-N pyraclofos Chemical compound C1=C(OP(=O)(OCC)SCCC)C=NN1C1=CC=C(Cl)C=C1 QHGVXILFMXYDRS-UHFFFAOYSA-N 0.000 description 1
- 229940015367 pyrethrum Drugs 0.000 description 1
- DWFZBUWUXWZWKD-UHFFFAOYSA-N pyridaben Chemical compound C1=CC(C(C)(C)C)=CC=C1CSC1=C(Cl)C(=O)N(C(C)(C)C)N=C1 DWFZBUWUXWZWKD-UHFFFAOYSA-N 0.000 description 1
- WJSXSXUHWBSPEP-UHFFFAOYSA-N pyridine;triphenylborane Chemical compound C1=CC=NC=C1.C1=CC=CC=C1B(C=1C=CC=CC=1)C1=CC=CC=C1 WJSXSXUHWBSPEP-UHFFFAOYSA-N 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- 125000005554 pyridyloxy group Chemical group 0.000 description 1
- ZLIBICFPKPWGIZ-UHFFFAOYSA-N pyrimethanil Chemical compound CC1=CC(C)=NC(NC=2C=CC=CC=2)=N1 ZLIBICFPKPWGIZ-UHFFFAOYSA-N 0.000 description 1
- 125000000714 pyrimidinyl group Chemical group 0.000 description 1
- YBBJKCMMCRQZMA-UHFFFAOYSA-N pyrithione Chemical class ON1C=CC=CC1=S YBBJKCMMCRQZMA-UHFFFAOYSA-N 0.000 description 1
- 229960003811 pyrithione disulfide Drugs 0.000 description 1
- XRJLAOUDSILTFT-UHFFFAOYSA-N pyroquilon Chemical compound O=C1CCC2=CC=CC3=C2N1CC3 XRJLAOUDSILTFT-UHFFFAOYSA-N 0.000 description 1
- 125000000168 pyrrolyl group Chemical group 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- MRUMAIRJPMUAPZ-UHFFFAOYSA-N quinolin-8-ol;sulfuric acid Chemical compound OS(O)(=O)=O.C1=CN=C2C(O)=CC=CC2=C1 MRUMAIRJPMUAPZ-UHFFFAOYSA-N 0.000 description 1
- FBQQHUGEACOBDN-UHFFFAOYSA-N quinomethionate Chemical compound N1=C2SC(=O)SC2=NC2=CC(C)=CC=C21 FBQQHUGEACOBDN-UHFFFAOYSA-N 0.000 description 1
- 238000010188 recombinant method Methods 0.000 description 1
- 230000001850 reproductive effect Effects 0.000 description 1
- 229960000329 ribavirin Drugs 0.000 description 1
- HZCAHMRRMINHDJ-DBRKOABJSA-N ribavirin Natural products O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1N=CN=C1 HZCAHMRRMINHDJ-DBRKOABJSA-N 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 235000020637 scallop Nutrition 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
- BHRZNVHARXXAHW-UHFFFAOYSA-N sec-butylamine Chemical compound CCC(C)N BHRZNVHARXXAHW-UHFFFAOYSA-N 0.000 description 1
- 229910052624 sepiolite Inorganic materials 0.000 description 1
- 235000019355 sepiolite Nutrition 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical group [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 229940014213 spinosad Drugs 0.000 description 1
- 235000015096 spirit Nutrition 0.000 description 1
- 125000003003 spiro group Chemical group 0.000 description 1
- PUYXTUJWRLOUCW-UHFFFAOYSA-N spiroxamine Chemical compound O1C(CN(CC)CCC)COC11CCC(C(C)(C)C)CC1 PUYXTUJWRLOUCW-UHFFFAOYSA-N 0.000 description 1
- 229960005322 streptomycin Drugs 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- JXHJNEJVUNHLKO-UHFFFAOYSA-N sulprofos Chemical compound CCCSP(=S)(OCC)OC1=CC=C(SC)C=C1 JXHJNEJVUNHLKO-UHFFFAOYSA-N 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000011269 tar Substances 0.000 description 1
- ZZYSLNWGKKDOML-UHFFFAOYSA-N tebufenpyrad Chemical compound CCC1=NN(C)C(C(=O)NCC=2C=CC(=CC=2)C(C)(C)C)=C1Cl ZZYSLNWGKKDOML-UHFFFAOYSA-N 0.000 description 1
- XQTLDIFVVHJORV-UHFFFAOYSA-N tecnazene Chemical compound [O-][N+](=O)C1=C(Cl)C(Cl)=CC(Cl)=C1Cl XQTLDIFVVHJORV-UHFFFAOYSA-N 0.000 description 1
- 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
- WWJZWCUNLNYYAU-UHFFFAOYSA-N temephos Chemical compound C1=CC(OP(=S)(OC)OC)=CC=C1SC1=CC=C(OP(=S)(OC)OC)C=C1 WWJZWCUNLNYYAU-UHFFFAOYSA-N 0.000 description 1
- IROINLKCQGIITA-UHFFFAOYSA-N terbutryn Chemical compound CCNC1=NC(NC(C)(C)C)=NC(SC)=N1 IROINLKCQGIITA-UHFFFAOYSA-N 0.000 description 1
- IWVCMVBTMGNXQD-UHFFFAOYSA-N terramycin dehydrate Natural products C1=CC=C2C(O)(C)C3C(O)C4C(N(C)C)C(O)=C(C(N)=O)C(=O)C4(O)C(O)=C3C(=O)C2=C1O IWVCMVBTMGNXQD-UHFFFAOYSA-N 0.000 description 1
- HVZJRWJGKQPSFL-UHFFFAOYSA-N tert-Amyl methyl ether Chemical compound CCC(C)(C)OC HVZJRWJGKQPSFL-UHFFFAOYSA-N 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
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 125000003831 tetrazolyl group Chemical group 0.000 description 1
- 239000004308 thiabendazole Substances 0.000 description 1
- 235000010296 thiabendazole Nutrition 0.000 description 1
- 229960004546 thiabendazole Drugs 0.000 description 1
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 1
- HOKKPVIRMVDYPB-UHFFFAOYSA-N thiacloprid Chemical compound C1=NC(Cl)=CC=C1CN1C(=NC#N)SCC1 HOKKPVIRMVDYPB-UHFFFAOYSA-N 0.000 description 1
- NWWZPOKUUAIXIW-FLIBITNWSA-N thiamethoxam Chemical compound [O-][N+](=O)\N=C/1N(C)COCN\1CC1=CN=C(Cl)S1 NWWZPOKUUAIXIW-FLIBITNWSA-N 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 125000005297 thienyloxy group Chemical group S1C(=CC=C1)O* 0.000 description 1
- DNVLJEWNNDHELH-UHFFFAOYSA-N thiocyclam Chemical compound CN(C)C1CSSSC1 DNVLJEWNNDHELH-UHFFFAOYSA-N 0.000 description 1
- BAKXBZPQTXCKRR-UHFFFAOYSA-N thiodicarb Chemical compound CSC(C)=NOC(=O)NSNC(=O)ON=C(C)SC BAKXBZPQTXCKRR-UHFFFAOYSA-N 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- OBZIQQJJIKNWNO-UHFFFAOYSA-N tolclofos-methyl Chemical compound COP(=S)(OC)OC1=C(Cl)C=C(C)C=C1Cl OBZIQQJJIKNWNO-UHFFFAOYSA-N 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical class CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- YWSCPYYRJXKUDB-KAKFPZCNSA-N tralomethrin Chemical compound CC1(C)[C@@H](C(Br)C(Br)(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 YWSCPYYRJXKUDB-KAKFPZCNSA-N 0.000 description 1
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 1
- BAZVSMNPJJMILC-UHFFFAOYSA-N triadimenol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC1=CC=C(Cl)C=C1 BAZVSMNPJJMILC-UHFFFAOYSA-N 0.000 description 1
- JWXZLCFGVKMEEK-UHFFFAOYSA-N triarathene Chemical compound C1=CC(Cl)=CC=C1C1=CC(C=2C=CC=CC=2)=C(C=2C=CC=CC=2)S1 JWXZLCFGVKMEEK-UHFFFAOYSA-N 0.000 description 1
- AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-UHFFFAOYSA-N 0.000 description 1
- IQGKIPDJXCAMSM-UHFFFAOYSA-N triazoxide Chemical compound N=1C2=CC=C(Cl)C=C2[N+]([O-])=NC=1N1C=CN=C1 IQGKIPDJXCAMSM-UHFFFAOYSA-N 0.000 description 1
- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
- WVZPYZMQQDNINJ-UHFFFAOYSA-N tributyl(butylstannyloxy)stannane Chemical compound CCCC[SnH](CCCC)O[SnH](CCCC)CCCC WVZPYZMQQDNINJ-UHFFFAOYSA-N 0.000 description 1
- YDUBPEZBWPRJJL-UHFFFAOYSA-M tributyl-(4-chloro-2-phenylphenoxy)stannane Chemical compound CCCC[Sn](CCCC)(CCCC)OC1=CC=C(Cl)C=C1C1=CC=CC=C1 YDUBPEZBWPRJJL-UHFFFAOYSA-M 0.000 description 1
- HFFZSMFXOBHQLV-UHFFFAOYSA-M tributylstannyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)CCCC HFFZSMFXOBHQLV-UHFFFAOYSA-M 0.000 description 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- YVWPNDBYAAEZBF-UHFFFAOYSA-N trimethylsilylmethanamine Chemical compound C[Si](C)(C)CN YVWPNDBYAAEZBF-UHFFFAOYSA-N 0.000 description 1
- IIYTXTQVIDHSSL-UHFFFAOYSA-N trimethylsilylmethanethiol Chemical compound C[Si](C)(C)CS IIYTXTQVIDHSSL-UHFFFAOYSA-N 0.000 description 1
- 238000002211 ultraviolet spectrum Methods 0.000 description 1
- 241000701447 unidentified baculovirus Species 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000003799 water insoluble solvent Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 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
- JLYXXMFPNIAWKQ-UHFFFAOYSA-N γ Benzene hexachloride Chemical compound ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- A01N55/00—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0803—Compounds with Si-C or Si-Si linkages
- C07F7/081—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
- C07F7/1804—Compounds having Si-O-C linkages
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
nは、1、2、3又は4を表し、
mは、1、2、3、4又は5を表し、
R1、R2、R3及びR4は、お互いから独立に、水素、アルキル、ハロゲノアルキル又はシクロアルキルを表し、
R5、R6及びR7は、お互いから独立に、アルキル又はアルコキシを表し、
Aは、−S(O)d−又は酸素を表し、
aは、1、2、3又は4を表し、但し、aが2、3又は4を表す場合、繰り返し単位−CR1R2−は同じ又は異なった意味を有してよく、
bは、0又は1を表し、
cは、0、1、2、3又は4を表し、但し、cが2、3又は4を表す場合、繰り返し単位−CR3R4−は同じ又は異なった意味を有してよく、
dは、0、1又は2を表す]
のフタルアミドを提供する。
のイミドを、式(III):
のシリルアミンと、適切な場合希釈剤の存在下で反応させることによって得られることが見出された。
Aは、硫黄又は酸素を表し、
bは、0又は1を表し、そして
X、R1、R2、R3、R4、R5、R6、R7、a及びcは、前記の意味を有する)
の化合物である。
Aは、硫黄又は酸素を表し、
bは、0又は1を表し、そして
X、R1、R2、R3、R4、R5、R6、R7、a及びcは、前記の意味を有する)
の化合物である。
Aが、SO又はSO2を表す
式(I−a)及び式(I−b)の化合物である。
Y1及びY2が、お互いから独立に、前記の基Yの好ましい、特に好ましい又は非常に特に好ましい意味を有し、
Aが、S(O)d又は酸素を表し、
bが、0又は1を表し、
dが、0、1又は2を表し、そして
X、R1、R2、R3、R4、R5、R6、R7、a及びcが、前記の好ましい、特に好ましい又は非常に特に好ましい意味を有する
式(I−a)及び式(I−b)の化合物である。
のシリルアミンは、例えば、式(IV):
のアジリジンを、式(V):
のチオールと、適切な場合には希釈剤(例えば、メタノール)の存在下で反応させることによって製造することができる(J.Org.Chem.l963年、第28巻、第l496頁参照)。
アルジモルフ(aldimorph)、アンプロピルホス(ampropylfos)、アンプロピルホス−カリウム、アンドプリム(andoprim)、アニラジン(anilazine)、アザコナゾール(azaconazole)、アゾキシストロビン(azoxystrobin)、ベナラキシル(benalaxyl)、ベノダニル(benodanil)、ベノミル(benomyl)、ベンザマクリル(benzamacril)、ベンザマクリル−イソブチル、ビアラホス(bialaphos)、ビナパクリル(binapacryl)、ビフェニル、ビテルタノール(bitertanol)、ブラスチシジン−S(blasticidin−S)、ブロムコナゾール(bromuconazole)、ブピリマート(bupirimate)、ブチオバート(buthiobate)、カルシウムポリスルフィド(calcium polysulphide)、カプシマイシン(capsimycin)、カプタフォル(captafol)、カプタン(captan)、カルベンダジム(carbendazim)、カルボキシン(carboxin)、カルボン(carvon)、キノメチオナート(quinomethionate)、クロベンチアゾン(chlobenthiazone)、クロルフェナゾール(chlorfenazole)、クロロネブ(chloroneb)、クロロピクリン、クロロタロニル(chlorothalonil)、クロゾリナート(chlozolinate)、クロジラコン(clozylacon)、クフラネブ(cufraneb)、シモキサニル(cymoxanil)、シプロコナゾール(cyproconazole)、シプロジニル(cyprodinil)、シプロフラム(cyprofuram)、デバカルブ(debacarb)、ジクロロフェン(dichlorophen)、ジクロブトラゾール(diclobutrazole)、ジクロフルアニド(diclofluanid)、ジクロメジン(diclomezine)、ジクロラン(dicloran)、ジエトフェンカルブ(diethofencarb)、ジフェノコナゾール(difenoconazole)、ジメチリモル(dimethirimol)、ジメトモルフ(dimethomorph)、ジニコナゾール(diniconazole)、ジニコナゾール−M、ジノカップ(dinocap)、ジフェニルアミン、ジピリチオン(dipyrithione)、ジタリムホス(ditalimfos)、ジチアノン(dithianon)、ドデモルフ(dodemorph)、ドジン(dodine)、ドラゾキソロン(drazoxolon)、エジフェンホス(edifenphos)、エポキシコナゾール(epoxiconazole)、エタコナゾール(etaconazole)、エチリモル(ethirimol)、エトリジアゾール(etridiazole)、ファモキサドン(famoxadon)、フェナパニル(fenapanil)、フェナリモル(fenarimol)、フェンブコナゾール(fenbuconazole)、フェンフラム(fenfuram)、フェニトロパン(fenitropan)、フェンピクロニル(fenpiclonil)、フェンプロピジン(fenpropidin)、フェンプロピモルフ(fenpropimorph)、酢酸フェンチン(fentin acetate)、水酸化フェンチン(fentin hydroxide)、フェルバム(ferbam)、フェリムゾン(ferimzone)、フルアジナム(fluazinam)、フルメトベル(flumetover)、フルオロミド(fluoromide)、フルキンコナゾール(fluquinconazole)、フルルプリミドール(flurprimidol)、フルシラゾール(flusilazole)、フルスルファミド(flusulphamide)、フルトラニル(flutolanil)、フルトリアフォル(flutriafol)、フォルペット(folpet)、フォセチル−アルミニウム(fosetyl−aluminium)、フォセチル−ナトリウム、フタリド(fthalide)、フベリダゾール(fuberidazole)、フララキシル(furalaxyl)、フラメトピル(furametpyr)、フルカルボニル(furcarbonil)、フルコナゾール(furconazole)、フルコナゾール−シス、フルメシクロックス(furmecyclox)、グアザチン(guazatine)、ヘキサクロロベンゼン、ヘキサコナゾール(hexaconazole)、ヒメキサゾール(hymexazole)、イマザリル(imazalil)、イミベンコナゾール(imibenconazole)、イミノクタジン(iminoctadine)、イミノクタジンアルベシラート(iminoctadine albesilate)、三酢酸イミノクタジン、ヨードカルブ(iodocarb)、イプコナゾール(ipconazole)、イプロベンホス(iprobenfos)(IBP)、イプロジオン(iprodione)、イルママイシン(irumamycin)、イソプロチオラン(isoprothiolane)、イソバレジオン(isovaledione)、カスガマイシン(kasugamycin)、クレソキシム−メチル(kresoxim−methyl)、銅製剤、例えば、水酸化銅、ナフテン酸銅、オキシ塩化銅、硫酸銅、酸化銅及びボルドー混合液、マンカッパー(mancopper)、マンコゼブ(mancozeb)、マネブ(maneb)、メフェリムゾン(meferimzone)、メパニピリム(mepanipyrim)、メプロニル(mepronil)、メタラキシル(metalaxyl)、メトコナゾール(metconazole)、メタスルホカルブ(methasulfocarb)、メトフロキサム(methfuroxam)、メチラム(metiram)、メトメクラム(metomeclam)、メトスルホバックス(metsulfovax)、ミルジオマイシン(mildiomycin)、マイクロブタニル(myclobutanil)、マイクロゾリン(myclozolin)、ジメチルジチオカルバミン酸ニッケル、ニトロタール−イソプロピル(nitrothal−isopropyl)、ヌアリモル(nuarimol)、オフレース(ofurace)、オキサジキシル(oxadixyl)、オキサモカルブ(oxamocarb)、オキソリン酸(oxolinic acid)、オキシカルボキシム(oxycarboxim)、オキシフェンチイン(oxyfenthiin)、パクロブトラゾール(paclobutrazole)、ペフラゾアート(pefurazoate)、ペンコナゾール(penconazole)、ペンシキュロン(pencycuron)、ホスジフェン(phosdiphen)、ピマリシン(pimaricin)、ピペラリン(piperalin)、ポリオキシン(polyoxin)、ポリオキソリム(polyoxorim)、プロベナゾール(probenazole)、プロクロラズ(prochloraz)、プロシミドン(procymidone)、プロパモカルブ(propamocarb)、プロパノシン−ナトリウム(propanosine−sodium)、プロピコナゾール(propiconazole)、プロピネブ(propineb)、ピラゾホス(pyrazophos)、ピリフェノックス(pyrifenox)、ピリメタニル(pyrimethanil)、ピロキロン(pyroquilon)、ピロキシフル(pyroxyfur)、キンコナゾール(quinconazole)、キントゼン(quintozene)(PCNB))、硫黄及び硫黄製剤、テブコナゾール(tebuconazole)、テクロフタラム(tecloftalam)、テクナゼン(tecnazene)、テトシクラシス(tetcyclasis)、テトラコナゾール(tetraconazole)、チアベンダゾール(thiabendazole)、チシオフェン(thicyofen)、チフルザミド(thifluzamide)、チオファナート−メチル(thiophanate−methyl)、チラム(thiram)、チオキシミド(tioxymid)、トルクロホス−メチル(tolclofos−methyl)、トリルフルアニド(tolylfluanid)、トリアジメフォン(triadimefon)、トリアジメノール(triadimenol)、トリアズブチル(triazbutil)、トリアゾキシド(triazoxide)、トリクラミド(trichlamide)、トリシクラゾール(tricyclazole)、トリデモルフ(tridemorph)、トリフルミゾール(triflumizole)、トリホリン(triforine)、トリチコナゾール(triticonazole)、ウニコナゾール(uniconazole)、バリダマイシンA(validamycin A)、ビンクロゾリン(vinclozolin)、ビニコナゾール(viniconazole)、ザリラミド(zarilamide)、ジネブ(zineb)、ジラム(ziram)及びまたダッガー(Dagger)G、OK−8705、OK−8801、
α−(1,1−ジメチルエチル)−β−(2−フェノキシエチル)−1H−1,2,4−トリアゾール−1−エタノール、
α−(2,4−ジクロロフェニル)−β−フルオロ−β−プロピル−1H−1,2,4−トリアゾール−1−エタノール、
α−(2,4−ジクロロフェニル)−β−メトキシ−α−メチル−1H−1,2,4−トリアゾール−1−エタノール、
α−(5−メチル−1,3−ジオキサン−5−イル)−β−[[4−(トリフルオロメチル)−フェニル]−メチレン]−1H−1,2,4−トリアゾール−1−エタノール、
(5RS,6RS)−6−ヒドロキシ−2,2,7,7−テトラメチル−5−(1H−1,2,4−トリアゾール−1−イル)−3−オクタノン、
(E)−α−(メトキシイミノ)−N−メチル−2−フェノキシ−フェニルアセトアミド、
1−イソプロピル{2−メチル−1−[[[1−(4−メチルフェニル)−エチル]−アミノ]−カルボニル]−プロピル}−カルバマート、
1−(2,4−ジクロロフェニル)−2−(1H−1,2,4−トリアゾール−1−イル)−エタノン−O−(フェニルメチル)−オキシム、
1−(2−メチル−1−ナフタレニル)−1H−ピロール−2,5−ジオン、
1−(3,5−ジクロロフェニル)−3−(2−プロペニル)−2,5−ピロリジンジオン、
1−[(ジヨードメチル)−スルホニル]−4−メチル−ベンゼン、
1−[[2−(2,4−ジクロロフェニル)−1,3−ジオキソラン−2−イル]−メチル]−1H−イミダゾール、
1−[[2−(4−クロロフェニル)−3−フェニルオキシラニル]−メチル]−1H−1,2,4−トリアゾール、
1−[1−[2−[(2,4−ジクロロフェニル)−メトキシ]−フェニル]−エテニル]−1H−イミダゾール、
1−メチル−5−ノニル−2−(フェニルメチル)−3−ピロリジノール、
2’,6’−ジブロモ−2−メチル−4’−トリフルオロメトキシ−4’−トリフルオロ−メチル−1,3−チアゾール−5−カルボキサニリド、
2,2−ジクロロ−N−[1−(4−クロロフェニル)−エチル]−1−エチル−3−メチル−シクロプロパンカルボキサミド、
2,6−ジクロロ−5−(メチルチオ)−4−ピリミジニル−チオシアナート、
2,6−ジクロロ−N−(4−トリフルオロメチルベンジル)−ベンズアミド、
2,6−ジクロロ−N−[[4−(トリフルオロメチル)−フェニル]−メチル]−ベンズアミド、
2−(2,3,3−トリヨード−2−プロペニル)−2H−テトラゾール、
2−[(1−メチルエチル)−スルホニル]−5−(トリクロロメチル)−1,3,4−チアジアゾール、
2−[[6−デオキシ−4−O−(4−O−メチル−β−D−グリコピラノシル)−α−D−グルコピラノシル]−アミノ]−4−メトキシ−1H−ピロロ[2,3−d]ピリミジン−5−カルボニトリル、
2−アミノブタン、
2−ブロモ−2−(ブロモメチル)−ペンタンニトリル、
2−クロロ−N−(2,3−ジヒドロ−1,1,3−トリメチル−1H−インデン−4−イル)−3−ピリジンカルボキサミド、
2−クロロ−N−(2,6−ジメチルフェニル)−N−(イソチオシアナトメチル)−アセタミド、
2−フェニルフェノール(OPP)、
3,4−ジクロロ−1−[4−(ジフルオロメトキシ)−フェニル]−1H−ピロール−2,5−ジオン、
3,5−ジクロロ−N−[シアノ[(1−メチル−2−プロピニル)−オキシ]−メチル]−ベンズアミド、
3−(1,1−ジメチルプロピル−1−オキソ−1H−インデン−2−カルボニトリル、
3−[2−(4−クロロフェニル)−5−エトキシ−3−イソキサゾリジニル]−ピリジン、
4−クロロ−2−シアノ−N,N−ジメチル−5−(4−メチルフェニル)−1H−イミダゾール−1−スルホンアミド、
4−メチル−テトラゾロ[1,5−a]キナゾリン−5(4H)−オン、
8−(1,1−ジメチルエチル)−N−エチル−N−プロピル−1,4−ジオキサスピロ[4,5]デカン−2−メタンアミン、
8−ヒドロキシキノリンスルファート、
9H−キサンテン−2−[(フェニルアミノ)−カルボニル]−9−カルボン酸ヒドラジド、
ビス−(1−メチルエチル)−3−メチル−4−[(3−メチルベンゾイル)−オキシ]−2,5−チオフェンジカルボキシラート、
シス−1−(4−クロロフェニル)−2−(1H−1,2,4−トリアゾール−1−イル)−シクロヘプタノール、
シス−4−[3−[4−(1,1−ジメチルプロピル)−フェニル−2−メチルプロピル]−2,6−ジメチル−モルホリン塩酸塩、
[(4−クロロフェニル)−アゾ]−シアノ酢酸エチル、
重炭酸カリウム、
メタンテトラチオールナトリウム塩、
メチル1−(2,3−ジヒドロ−2,2−ジメチル−1H−インデン−1−イル)−1H−イミダゾール−5−カルボキシラート、
メチルN−(2,6−ジメチルフェニル)−N−(5−イソキサゾリルカルボニル)−DL−アラニナート、
メチルN−(クロロアセチル)−N−(2,6−ジメチルフェニル)−DL−アラニナート、
N−(2,3−ジクロロ−4−ヒドロキシフェニル)−1−メチル−シクロヘキサンカルボキサミド、
N−(2,6−ジメチルフェニル)−2−メトキシ−N−(テトラヒドロ−2−オキソ−3−フラニル)−アセタミド、
N−(2,6−ジメチルフェニル)−2−メトキシ−N−(テトラヒドロ−2−オキソ−3−チエニル)−アセタミド、
N−(2−クロロ−4−ニトロフェニル)−4−メチル−3−ニトロ−ベンゼンスルホンアミド、
N−(4−シクロヘキシルフェニル)−1,4,5,6−テトラヒドロ−2−ピリミジンアミン、
N−(4−ヘキシルフェニル)−1,4,5,6−テトラヒドロ−2−ピリミジンアミン
N−(5−クロロ−2−メチルフェニル)−2−メトキシ−N−(2−オキソ−3−オキサゾリジニル)−アセタミド、
N−(6−メトキシ−3−ピリジニル)−シクロプロパンカルボキサミド、
N−[2,2,2−トリクロロ−1−[(クロロアセチル)−アミノ]−エチル]−ベンズアミド、
N−[3−クロロ−4,5−ビス(2−プロピニルオキシ)−フェニル]−N’−メトキシ−メタンイミドアミド、
N−ホルミル−N−ヒドロキシ−DL−アラニン−ナトリウム塩、
O,O−ジエチル[2−(ジプロピルアミノ)−2−オキソエチル]−エチルホスホルアミドチオアート、
O−メチルS−フェニル フェニルプロピルホスホルアミドチオアート、
S−メチル1,2,3−ベンゾチアジアゾール−7−カルボチオアート、
スピロ[2H]−1−ベンゾピラン−2,1’(3’H)−イソベンゾフラン]−3’−オン。
ブロノポル(bronopol)、ジクロロフェン、ニトラピリン(nitrapyrin)、ジメチルジチオカルバミン酸ニッケル、カスガマイシン、オクチリノン(octhilinone)、フランカルボン酸、オキシテトラサイクリン、プロベナゾール、ストレプトマイシン、テクロフタラム、硫酸銅及び他の銅製剤。
アバメクチン(abamectin)、アセファト(acephat)、アセタミプリド(acetamiprid)、アクリナトリン(acrinathrin)、アラニカルブ(alanycarb)、アルジカルブ(aldicarb)、アルドキシカルブ(aldoxycarb)、α−シペルメトリン(alpha−cypermethrin)、アルファメトリン(alphamethrin)、アミトラズ(amitraz)、アベルメクチン(avermectin)、AZ60541、アザジラクチン(azadirachtin)、アザメチホス(azamethiphos)、アジンホスA(azinphos A)、アジンホスM、アゾシクロチン(azocyclotin)、バチルス・ポピリアエ(Bacillus popilliae)、バチルス・スファエリクス(Bacillus sphaericus)、バチルス・スブチルス(Bacillus subtilis)、バチルス・ツリンギエンシス(Bacillus thuringiensis)、バクロウイルス、ボーバリア・バッシアナ(Beauveria bassiana)、ボーバリア・テネラ(Beauveria tenella)、ベンジオカルブ(bendiocarb)、ベンフラカルブ(benfuracarb)、ベンスルタプ(bensultap)、ベンズオキシマート、ベータシフルトリン(betacyfluthrin)、ビフェナザート(bifenazate)、ビフェントリン(bifenthrin)、ビオエタノメトリン(bioethanomethrin)、ビオペルメトリン(biopermethrin)、BPMC、ブロモホスA(bromophos A)、ブフェンカルブ(bufencarb)、ブプロフェジン(buprofezin)、ブタチオホス(butathiofos)、ブトカルボキシム(butocarboxim)、ブチルピリダベン(butylpyridaben)、カデュサホス(cadusafos)、カルバリール(carbaryl)、カルボフラン(carbofuran)、カルボフェノチオン(carbophenothion)、カルボスルフハン(carbosulfhan)、カルタプ(cartap)、クロエトカルブ(chloethocarb)、クロレトキシホス(chlorethoxyfos)、クロルフェナピル(chlorfenapyr)、クロルフェンビンホス(chlorfenvinphos)、クロルフルアズロン(chlorfluazuron)、クロルメホス(chlormephos)、クロルピリホス(chlorpyrifos)、クロルピリホスM、クロバポルトリン(chlovaporthrin)、クロマフェノジド(chromafenozide)、シス−レスメトリン(cis−resmethrin)、シスペルメトリン(cispermethrin)、クロシトリン(clocythrin)、クロエトカルブ(cloethocarb)、クロフェンテジン(clofentezin)、クロチアニジン(clothianidine)、シアノホス(cyanophos)、シクロプレン(cycloprene)、シクロプロトリン(cycloprothrin)、シフルトリン(cyfluthrin)、シハロトリン(cyhalothrin)、シヘキサチン(cyhexatin)、シペルメトリン(cypermethrin)、シロマジン(cyromazine)、デルタメトリン(deltamethrin)、デメトンM(demeton M)、デメトンS、デメトン−S−メチル(demeton−S−methyl)、ジアフェンチウロン(diafenthiuron)、ジアジノン(diazinon)、ジクロルボス(dichlorvos)、ジフルベンズロン(diflubenzuron)、ジメトアート(dimethoate)、ジメチルビンホス(dimethylvinphos)、ジオフェノラン(diofenolan)、ジスルホトン(disulfoton)、ドクサト−ナトリウム(docusat−sodium)、ドフェナピン(dofenapyn)、エフルシラナート(eflusilanate)、エマメクチン(emamectin)、エムペントリン(empenthrin)、エンドスルファン(endosulfan)、エントモプフトラ種(Entomopfthora spp.)、エプリノメクチン(eprinomectin)、エスフェンバレラート(esfenvalerate)、エチオフェンカルブ(ethiofencarb)、エチオン(ethion)、エトプロホス(ethoprophos)、エトフェンプロクス(ethofenprox)、エトキサゾール(etoxazole)、エトリムホス(etrimfos)、フェナミホス(fenamiphos)、フェナザキン(fenazaquin)、フェンブタチンオキシド(fenbutatin oxide)、フェニトロチオン(fenitrothion)、フェノチオカルブ(fenothiocarb)、フェノキサクリム(fenoxacrim)、フェノキシカルブ(fenoxycarb)、フェンプロパトリン(fenpropathrin)、フェンピラド(fenpyrad)、フェンピリトリン(fenpyrithrin)、フェンピロキシマート(fenpyroximate)、フェンバレラート(fenvalerate)、フィプロニル(fipronil)、フルアズロン(fluazuron)、フルブロシトリナート(flubrocythrinate)、フルシクロクスロン(flucycloxuron)、フルシトリナート(flucythrinate)、フルフェノクスロン(flufenoxuron)、フルテンジン(flutenzine)、フルバリナート(fluvalinate)、ホノホス(fonophos)、ホスメチラン(fosmethilan)、ホスチアザート(fosthiazate)、フブフェンプロクス(fubfenprox)、フラチオカルブ(furathiocarb)、顆粒症ウイルス、ハロフェノジド(halofenozide)、HCH、ヘプテノホス(heptenophos)、ヘキサフルムロン(hexaflumuron)、ヘキシチアゾクス(hexythiazox)、ヒドロプレン(hydroprene)、イミダクロプリド(imidacloprid)、イサゾホス(isazofos)、イソフェンホス(isofenphos)、イソキサチオン(isoxathion)、イベルメクチン(ivermectin)、核ポリヘドロシスウイルス(nuclear polyhedrosis viruses)、λ−シハロトリン(lambda−cyhalothrin)、ルフェヌロン(lufenuron)、マラチオン(malathion)、メカルバム(mecarbam)、メタルデヒド(metaldehyde)、メタミドホス(methamidophos)、メタリジウム・アニソプリアエ(Metharhizium anisopliae)、メタリジウム・フラボビリド(Metharhizium flavoviride)、メチダチオン(methidathion)、メチオカルブ(methiocarb)、メトミル(methomyl)、メトキシフェノジド(methoxyfenozide)、メトルカルブ(metolcarb)、メトキサジアゾン(metoxadiazone)、メビンホス(mevinphos)、ミルベメクチン(milbemectin)、ミルベマイシン(milbemycin)、モノクロトホス(monocrotophos)、ナレド(naled)、ニテンピラム(nitenpyram)、ニチアジン(nithiazine)、ノバルロン(novaluron)、オメトアート(omethoate)、オキサミル(oxamyl)、オキシデメトンM(oxydemethon M)、パエシロマイセス・フモソロセウス(Paecilomyces fumosoroseus)、パラチオンA(parathion A)、パラチオンM、ペルメトリン(permethrin)、フェントアート(phenthoate)、ホラート(phorate)、ホサロン(phosalone)、ホスメト(phosmet)、ホスファミドン(phosphamidon)、ホキシム(phoxim)、ピリミカルブ(pirimicarb)、ピリミホスA(pirimiphos A)、ピリミホスM、プロフェノホス(profenofos)、プロメカルブ(promecarb)、プロポクスル(propoxur)、プロチオホス(prothiofos)、プロトアート(prothoate)、ピメトロジン(pymetrozine)、ピラクロホス(pyraclofos)、ピレスメトリン(pyresmethrin)、ピレトルム(pyrethrum)、ピリダベン(pyridaben)、ピリダチオン(pyridathion)、ピリミジフェン(pyrimidifen)、ピリプロキシフェン(pyriproxyfen)、キナルホス(quinalphos)、リバビリン(ribavirin)、サリチオン(salithion)、セブホス(sebufos)、シラフルオフェン(silafluofen)、スピノサド(spinosad)、スルホテプ(sulphotep)、スルプロホス(sulprofos)、τ−フルバリナート(tau−fluvarinate)、テブフェノジド(tebufenozide)、テブフェンピラド(tebufenpyrad)、テブピリミホス(tebupirimiphos)、テフルベンズロン(teflubenzuron)、テフルトリン(tefluthrin)、テメホス(temephos)、テミビンホス(temivinphos)、テルブホス(terbufos)、テトラクロルビンホス(tetrachlorvinphos)、θ−シペルメトリン、チアメトキサム(thiamethoxam)、チアプロニル(thiapronil)、チアトリホス(thiatriphos)、チオシクラム水素オキサラート(thiocyclam hydrogen oxalate)、チオジカルブ(thiodicarb)、チオファノクス(thiofanox)、ツリンギエンシン(thuringiensin)、トラロシトリン(tralocythrin)、トラロメトリン(tralomethrin)、トリアラテン(triarathen)、トリアザマート(triazamate)、トリアゾホス(triazophos)、トリアズロン(triazuron)、トリクロフェニジン(trichlophenidine)、トリクロルフォン(trichlorfon)、トリフルムロン(triflumuron)、トリメタカルブ(trimethacarb)、バミドチオン(Vamidothion)、バニリプロール(vaniliprole)、ベルチシリウム レカニイ(Verticillium lecanii)、YI5302、ζ−シペルメトリン、ゾラプロホス(zolaprofos)、
(1R−シス)−[5−(フェニルメチル)−3−フラニル]−メチル13−[(ジヒドロ−2−オキソ−3(2H)−フラニリデン)−メチル]−2,2−ジメチルシクロプロパンカルボキシラート、
(3−フェノキシフェニル)−メチル2,2,3,3−テトラメチルシクロプロパンカルボキシラート、
1−[(2−クロロ−5−チアゾリル)メチル]テトラヒドロ−3,5−ジメチル−N−ニトロ−1,3,5−トリアジン−2(1H)−イミン、
2−(2−クロロ−6−フルオロフェニル)−4−[4−(1,1−ジメチルエチル)フェニル]−4,5−ジヒドロ−オキサゾール、
2−(アセチルオキシ)−3−ドデシル−1,4−ナフタレンジオン、
2−クロロ−N−[[[4−(1−フェニルエトキシ)−フェニル]−アミノ]−カルボニル]−ベンズアミド、
2−クロロ−N−[[[4−(2,2−ジクロロ−1,1−ジフルオロエトキシ)−フェニル]−アミノ]−カルボニル]−ベンズアミド、
3−メチルフェニル プロピルカルバマート、
4−[4−(4−エトキシフェニル)−4−メチルフェニル]−1−フルオロ−2−フェノキシ−ベンゼン、
4−クロロ−2−(1,1−ジメチルエチル)−5−[[2−(2,6−ジメチル−4−フェノキシフェノキシ)エチル]チオ]−3(2H)−ピリダジノン、
4−クロロ−2−(2−クロロ−2−メチルプロピル)−5−[(6−ヨード−3−ピリジニル)メトキシ]−3(2H)−ピリダジノン、
4−クロロ−5−[(6−クロロ−3−ピリジニル)メトキシ]−2−(3,4−ジクロロフェニル)−3(2H)−ピリダジノン、
バチルス・ツリンギエンシス株EG−2348、
[2−ベンゾイル−1−(1,1−ジメチルエチル)−ヒドラジノ安息香酸、
2,2−ジメチル−3−(2,4−ジクロロフェニル)−2−オキソ−1−オキサスピロ[4,5]デク−3−エン−4−イルブタノアート、
[3−[(6−クロロ−3−ピリジニル)メチル]−2−チアゾリジニリデン]−シアナミド、
ジヒドロ−2−(ニトロメチレン)−2H−1,3−チアジン−3(4H)−カルボキサルデヒド、
エチル[2−[[1,6−ジヒドロ−6−オキソ−1−(フェニルメチル)−4−ピリダジニル]オキシ]エチル]−カルバマート、
N−(3,4,4−トリフルオロ−1−オキソ−3−ブテニル)−グリシン、
N−(4−クロロフェニル)−3−[4−(ジフルオロメトキシ)フェニル]−4,5−ジヒドロ−4−フェニル−1H−ピラゾール−1−カルボキサミド、
N−[(2−クロロ−5−チアゾリル)メチル]−N’−メチル−N”−ニトロ−グアニジン、
N−メチル−N’−(1−メチル−2−プロペニル)−1,2−ヒドラジンジカルボチオアミド、
N−メチル−N’−2−プロペニル−1,2−ヒドラジンジカルボチオアミド、
O,O−ジエチル[2−(ジプロピルアミノ)−2−オキソエチル]−エチルホスホルアミドチオアート。
Hylotrupes bajulus、Chlorophorus pilosis、Anobium punctatum、Xestobium rufovillosum、Ptilinus pecticornis、Dendrobium pertinex、Ernobius mollis、Priobium carpini、Lyctus brunneus、Lyctus africanus、Lyctus planicollis、Lyctus linearis、Lyctus pubescens、Trogoxylon aequale、Minthes rugicollis、Xyleborus spec.、Tryptodendron spec.、Apate monachus、Bostrychus capucins、Heterobostrychus brunneus、Sinoxylon spec.、Dinoderus minutus。
Sirex juvencus、Urocerus gigas、Urocerus gigas taignus、Urocerus augur。
Kalotermes flavicollis、Cryptotermes brevis、Heterotermes indicola、Reticulitermes flavipes、Reticulitermes santonensis、Reticulitermes lucifugus、Mastotermes darwiniensis、Zootermopsis nevadensis、Coptotermes formosanus。
2−tert−ブチルアミノ−4−シクロプロピルアミノ−6−メチルチオ−1,3,5−トリアジン、ジクロロフェン、ジウロン(diuron)、エンドタール(endothal)、酢酸フェンチン、イソプロツロン(isoproturon)、メタベンズチアズロン(methabenzthiazuron)、オキシフルオルフェン(oxyfluorfen)、キノクラミン(quinoclamine)及びテルブトリン(terbutryn);
殺真菌剤、例えば、
ベンゾ[b]チオフェンカルボン酸シクロヘキシルアミドS,S−ジオキシド、ジクロフルアニド、フルオルフォルペット(fluorfolpet)、3−ヨード−2−プロピニル−ブチルカルバマート、トリルフルアニド並びにアザコナゾール、シプロコナゾール、エポキシコナゾール、ヘキサコナゾール、メトコナゾール、プロピコナゾール及びテブコナゾールのようなアゾール;
殺陸貝剤、例えば、
酢酸フェンチン、メタルデヒド、メチオカルブ、ニクロサミド(niclosamid)、チオジカルブ及びトリメタカルブ;
又は、一般的な防汚活性化合物、例えば、
4,5−ジクロロ−2−オクチル−4−イソチアゾリン−3−オン、ジヨードメチルパラトリルスルホン、2−(N,N−ジメチルチオカルバモイルチオ)−5−ニトロチアジル、2−ピリジンチオール1−オキシドのカリウム、銅、ナトリウム及び亜鉛塩、ピリジン−トリフェニルボラン、テトラブチルジスタンノキサン、2,3,5,6−テトラクロロ−4−(メチルスルホニル)−ピリジン、2,4,5,6−テトラクロロイソフタロニトリル、テトラメチルチウラムジスルフィド及び2,4,6−トリクロロフェニルマレイミド。
3−クロロ−N2−{2−メチル−4−[1,2,2,2−テトラフルオロ−1−(トリフルオロメチル)エチル]フェニル}−N1−(1−メチル−2−{[(トリメチルシリル)メチル]スルファニル}エチル)フタルアミド
収量:0.12g(理論量の15%)
m.p.:159℃から160℃
HPLC:logP(pH2.3)=5.38
1H−NMR(CD3CN):δ=0(9H),1.15(d,3H),1.74(m,2H),2.32(s,3H),2.55(m,1H),2.65(m,1H),4.14(m,1H),6.85(m,1H),7.55(m,5H),8.05(m,1H),8.30(m,1H)ppm。
3−クロロ−N1−{2−メチル−4−[1,2,2,2−テトラフルオロ−1−(トリフルオロメチル)エチル]フェニル}−N2−(1−メチル−2−{[(トリメチルシリル)メチル]スルファニル}エチル)フタルアミド
収量:0.20g(理論量の27%)
m.p.:161℃から162℃
HPLC:logP(pH2.3)=5.56
1H−NMR(CD3CN):δ=0(9H),1.15(d,3H),1.75(m,2H),2.35(s,3H),2.5(m,1H),2.65(m,1H),4.15(m,1H),6.95(m,1H),7.55(m,3H),7.65(m,1H),7.75(m,1H),8.15(m,1H),8.55(m,1H)ppm。
3−クロロ−N1−[2−メチル−4−(1,1,2,2−テトラフルオロエトキシ)フェニル]−N2−[(トリメチルシリル)メチル]フタルアミド(異性体1)及び3−クロロ−N2−[2−メチル−4−(1,1,2,2−テトラフルオロエトキシ)フェニル]−N1−[(トリメチルシリル)メチル]フタルアミド(異性体2)
収量:0.55g(理論量の56%)
HPLC:logP(pH2.3)=3.59及び3.69
1H−NMR(CD3CN):δ=0.1(9H),2.25(s,3H),2.75(s,2H),6.12(m,1H),6.7−8.5(m,8H)ppm。
3−クロロ−N1−{2−メチル−4−[1,2,2,2−テトラフルオロ−1−(トリフルオロメチル)エチル]フェニル}−N2−{2−メチル−2−[(トリメチルシリル)オキシ]プロピル}フタルアミド
収量:0.42g(理論量の23%)
m.p.:144℃から145℃
HPLC:logP(pH2.3)=3.11
1H−NMR(CD3CN):δ=0(9H),1.15(s,6H),2.3(s,3H),3.2(m,2H),6.70−8.50(m,8H)。
3−クロロ−N2−{2−メチル−4−[1,2,2,2−テトラフルオロ−1−(トリフルオロメチル)エチル]フェニル}−N1−{2−メチル−2−[(トリメチルシリル)オキシ]プロピル}フタルアミド
収量:0.27g(理論量の22%)
m.p.:163℃から164℃
HPLC:logP(pH2.3)=3.19
1H−NMR(CD3CN):δ=0(9H),1.1(s,3H),1.15(s,3H),2.3(s,3H),3.25(m,2H),6.95(m,1H),7.45(m,3H),7.60(m,2H),7.95(m,1H),8.35(m,1H)ppm。
HPLC:logP(pH2.3)=1.28
1H−NMR(CD3CN):δ=0.05(9H),1.15(d,3H),1.75(q,2H),2.50(m,2H),2.85(br,2H),3.10(m,1H)ppm。
(実施例A)
Heliothis virescens試験
溶媒:7重量部のジメチルホルムアミド
乳化剤:2重量部のアルキルアリールポリグリコールエーテル
活性化合物の適切な製剤を製造するために、1重量部の活性化合物を、記載した量の溶媒及び乳化剤と混合し、このコンセントレートを、乳化剤含有水で所望の濃度まで希釈する。
Phaedon幼虫試験
溶媒:7重量部のジメチルホルムアミド
乳化剤:2重量部のアルキルアリールポリグリコールエーテル
活性化合物の適切な製剤を製造するために、1重量部の活性化合物を、記載した量の溶媒及び乳化剤と混合し、このコンセントレートを、乳化剤含有水で所望の濃度まで希釈する。
Plutella試験、感受性系統
溶媒:7重量部のジメチルホルムアミド
乳化剤:2重量部のアルキルアリールポリグリコールエーテル
活性化合物の適切な製剤を製造するために、1重量部の活性化合物を、記載した量の溶媒及び乳化剤と混合し、このコンセントレートを、乳化剤含有水で所望の濃度まで希釈する。
Plutella試験、抵抗性系統
溶媒:7重量部のジメチルホルムアミド
乳化剤:2重量部のアルキルアリールポリグリコールエーテル
活性化合物の適切な製剤を製造するために、1重量部の活性化合物を、記載した量の溶媒及び乳化剤と混合し、このコンセントレートを、乳化剤含有水で所望の濃度まで希釈する。
Spodoptera exigua試験
溶媒:7重量部のジメチルホルムアミド
乳化剤:2重量部のアルキルアリールポリグリコールエーテル
活性化合物の適切な製剤を製造するために、1重量部の活性化合物を、記載した量の溶媒及び乳化剤と混合し、このコンセントレートを、乳化剤含有水で所望の濃度まで希釈する。
Spodoptera frugiperda試験
溶媒:7重量部のジメチルホルムアミド
乳化剤:2重量部のアルキルアリールポリグリコールエーテル
活性化合物の適切な製剤を製造するために、1重量部の活性化合物を、記載した量の溶媒及び乳化剤と混合し、このコンセントレートを、乳化剤含有水で所望の濃度まで希釈する。
Diabrotica balteata試験(土壌中の幼虫)
臨界濃度試験/土壌昆虫−トランスジェニック植物の処理
溶媒:7重量部のジメチルホルムアミド
乳化剤:1重量部のアルキルアリールポリグリコールエーテル
活性化合物の適切な製剤を製造するために、1重量部の活性化合物を、記載した量の溶媒、記載した量の乳化剤と混合し、このコンセントレートを、乳化剤含有水で所望の濃度まで希釈する。
Heliothis virescens試験(トランスジェニック植物の処理)
溶媒:7重量部のジメチルホルムアミド
乳化剤:1重量部のアルキルアリールポリグリコールエーテル
活性化合物の適切な製剤を製造するために、1重量部の活性化合物を、記載した量の溶媒及び乳化剤と混合し、このコンセントレートを、乳化剤含有水で所望の濃度まで希釈する。
Claims (6)
- 式(I):
X及びYが、更に、お互いから独立に、フェニル、フェノキシ、ヘテロアリール又はヘテロアリールオキシを表し、これらのそれぞれは、置換されていないか、またはC1〜C6−アルコキシ、C1〜C6−ハロゲノアルコキシ、C1〜C6−アルキルチオ及びC1〜C6−ハロゲノアルキルチオからなる群からの同じ又は異なった置換基により一から四置換されており、
nが、1、2又は3を表し、
mが、1、2、3又は4を表し、
R1、R2、R3及びR4が、お互いから独立に、水素、C1〜C6−アルキル、C1〜C6−ハロゲノアルキル又はC3〜C6−シクロアルキルを表し、
R5、R6及びR7が、お互いから独立に、C1〜C6−アルキル又はC1〜C6−アルコキシを表し、
Aが、−S(O)d−又は酸素を表し、
aが、1、2、3又は4を表し、但し、aが2、3又は4を表す場合、繰り返し単位−CR1R2−は同じ又は異なった意味を有してよく、
bが、0又は1を表し、
cが、0、1、2、3又は4を表し、但し、cが2、3又は4を表す場合、繰り返し単位−CR3R4−は同じ又は異なった意味を有してよく、
dが、0、1又は2を表す]
のフタルアミド。 - 式(II):
のイミドを、式(III):
のシリルアミンと、適切な場合希釈剤の存在下で反応させることを特徴とする、請求項1に記載の式(I)の化合物の製造方法。 - エキステンダー及び/又は界面活性剤に加えて、少なくとも1種の請求項1に記載の式(I)の化合物を含有することを特徴とする、病虫害防除剤。
- 害虫を駆除するための、請求項1に記載の式(I)の化合物の使用。
- 請求項1に記載の式(I)の化合物を、害虫及び/又はそれらの生息環境に作用させることを特徴とする、害虫の駆除方法。
- 請求項1に記載の式(I)の化合物を、エキステンダー及び/又は界面活性剤と混合することを特徴とする、病虫害防除剤の製造方法。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE10105169 | 2001-02-06 | ||
DE10115406A DE10115406A1 (de) | 2001-02-06 | 2001-03-29 | Phthalsäurediamide |
PCT/EP2002/000809 WO2002062807A1 (de) | 2001-02-06 | 2002-01-25 | Phthalsäurediamide, ein verfahren zu ihrer herstellung und ihre verwendung als schädlingsbekämpfungsmittel |
Publications (3)
Publication Number | Publication Date |
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JP2004526703A JP2004526703A (ja) | 2004-09-02 |
JP2004526703A5 JP2004526703A5 (ja) | 2005-12-22 |
JP4165808B2 true JP4165808B2 (ja) | 2008-10-15 |
Family
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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JP2002563159A Expired - Fee Related JP4165808B2 (ja) | 2001-02-06 | 2002-01-25 | フタル酸ジアミド、該生成物の製造方法及び害虫を駆除するためのその使用 |
Country Status (11)
Country | Link |
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US (1) | US6835847B2 (ja) |
EP (1) | EP1360190B1 (ja) |
JP (1) | JP4165808B2 (ja) |
CN (1) | CN1310926C (ja) |
AT (1) | ATE304018T1 (ja) |
BR (1) | BR0206964A (ja) |
DE (1) | DE50204181D1 (ja) |
ES (1) | ES2245398T3 (ja) |
IL (1) | IL157046A0 (ja) |
MX (1) | MXPA03006996A (ja) |
WO (1) | WO2002062807A1 (ja) |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
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EP1538138A4 (en) * | 2002-08-26 | 2007-07-25 | Nissan Chemical Ind Ltd | SUBSTITUTED BENZANILIDE COMPOUND AND PROTECTIVE AGENTS |
US7211270B2 (en) | 2002-10-04 | 2007-05-01 | E. I. Du Pont De Nemours And Company | Anthranilamide insecticides |
DE10330724A1 (de) | 2003-07-08 | 2005-01-27 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
DE10330723A1 (de) * | 2003-07-08 | 2005-02-03 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
JP2005114718A (ja) * | 2003-10-10 | 2005-04-28 | Bayer Cropscience Ag | 殺虫剤活性化合物を特定するための方法 |
DE102004035134A1 (de) | 2004-07-20 | 2006-02-16 | Bayer Cropscience Ag | Selektive Insektizide auf Basis von Halogenalkylnicotinsäurederivaten, Anthranilsäureamiden oder Phthalsäurediamiden und Safenern |
DE102005059466A1 (de) * | 2005-12-13 | 2007-06-14 | Bayer Cropscience Ag | Insektizide Zusammensetzungen mit verbesserter Wirkung |
KR20090060446A (ko) * | 2006-09-30 | 2009-06-12 | 바이엘 크롭사이언스 아게 | 재배 기재에 적용시 농약 조성물의 생물학적 작용 개선, 적합한 제제 및 그의 용도 |
EP2129225B1 (en) | 2007-04-03 | 2012-12-05 | E. I. Du Pont de Nemours and Company | Substituted benzene fungicides |
US7652116B2 (en) * | 2007-06-20 | 2010-01-26 | 3M Innovative Properties Company | Fluorochemical urethane-silane compounds and aqueous compositions thereof |
JP6269875B2 (ja) * | 2017-03-09 | 2018-01-31 | 信越化学工業株式会社 | 有機ケイ素化合物およびその製造方法 |
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CN1025470C (zh) * | 1986-05-31 | 1994-07-20 | 赫彻斯特股份公司 | 含新型硅烷衍生物的农药,杀虫剂和杀螨剂组合物 |
GB8820129D0 (en) | 1988-08-24 | 1988-09-28 | Schering Agrochemicals Ltd | Fungicides |
JPH0474187A (ja) * | 1990-07-12 | 1992-03-09 | Toshiba Silicone Co Ltd | フタルイミド基を有するシラン |
TW515786B (en) | 1997-11-25 | 2003-01-01 | Nihon Nohyaku Co Ltd | Phthalic acid diamide derivatives, agricultural and horticultural insecticides, and a method for application of the insecticides |
CZ299375B6 (cs) | 1998-11-30 | 2008-07-09 | Nihon Nohyaku Co., Ltd. | Ftalamidové deriváty nebo jejich soli, zemedelsko-zahradnický insekticid je obsahující a jeho použití |
-
2002
- 2002-01-25 DE DE50204181T patent/DE50204181D1/de not_active Expired - Lifetime
- 2002-01-25 BR BR0206964-4A patent/BR0206964A/pt not_active Application Discontinuation
- 2002-01-25 IL IL15704602A patent/IL157046A0/xx unknown
- 2002-01-25 CN CNB028078209A patent/CN1310926C/zh not_active Expired - Fee Related
- 2002-01-25 WO PCT/EP2002/000809 patent/WO2002062807A1/de active IP Right Grant
- 2002-01-25 AT AT02703581T patent/ATE304018T1/de not_active IP Right Cessation
- 2002-01-25 JP JP2002563159A patent/JP4165808B2/ja not_active Expired - Fee Related
- 2002-01-25 US US10/467,018 patent/US6835847B2/en not_active Expired - Fee Related
- 2002-01-25 EP EP02703581A patent/EP1360190B1/de not_active Expired - Lifetime
- 2002-01-25 ES ES02703581T patent/ES2245398T3/es not_active Expired - Lifetime
- 2002-01-25 MX MXPA03006996A patent/MXPA03006996A/es active IP Right Grant
Also Published As
Publication number | Publication date |
---|---|
DE50204181D1 (de) | 2005-10-13 |
BR0206964A (pt) | 2004-03-09 |
CN1310926C (zh) | 2007-04-18 |
JP2004526703A (ja) | 2004-09-02 |
CN1500092A (zh) | 2004-05-26 |
WO2002062807A1 (de) | 2002-08-15 |
US6835847B2 (en) | 2004-12-28 |
ES2245398T3 (es) | 2006-01-01 |
US20040077597A1 (en) | 2004-04-22 |
EP1360190A1 (de) | 2003-11-12 |
IL157046A0 (en) | 2004-02-08 |
EP1360190B1 (de) | 2005-09-07 |
ATE304018T1 (de) | 2005-09-15 |
MXPA03006996A (es) | 2003-11-18 |
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