JP5876209B2 - 殺微生物剤の新規な固体形態 - Google Patents
殺微生物剤の新規な固体形態 Download PDFInfo
- Publication number
- JP5876209B2 JP5876209B2 JP2009553032A JP2009553032A JP5876209B2 JP 5876209 B2 JP5876209 B2 JP 5876209B2 JP 2009553032 A JP2009553032 A JP 2009553032A JP 2009553032 A JP2009553032 A JP 2009553032A JP 5876209 B2 JP5876209 B2 JP 5876209B2
- Authority
- JP
- Japan
- Prior art keywords
- formula
- compound
- syn
- racemic
- modification
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- 239000007787 solid Substances 0.000 title description 37
- 230000003641 microbiacidal effect Effects 0.000 title 1
- 229940124561 microbicide Drugs 0.000 title 1
- 239000002855 microbicide agent Substances 0.000 title 1
- 230000004048 modification Effects 0.000 claims description 93
- 238000012986 modification Methods 0.000 claims description 93
- 239000000203 mixture Substances 0.000 claims description 90
- 239000013078 crystal Substances 0.000 claims description 57
- 239000000463 material Substances 0.000 claims description 38
- 238000000634 powder X-ray diffraction Methods 0.000 claims description 21
- 239000004480 active ingredient Substances 0.000 claims description 20
- 238000000034 method Methods 0.000 claims description 15
- 244000045561 useful plants Species 0.000 claims description 9
- 201000010099 disease Diseases 0.000 claims description 8
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 8
- 230000000844 anti-bacterial effect Effects 0.000 claims description 6
- 238000010586 diagram Methods 0.000 claims description 4
- 244000000003 plant pathogen Species 0.000 claims description 4
- YHOQMAJZIIUYAZ-UHFFFAOYSA-N C1=CC=C(N)C2=C1C1C(C(C)C)C2CC1 Chemical compound C1=CC=C(N)C2=C1C1C(C(C)C)C2CC1 YHOQMAJZIIUYAZ-UHFFFAOYSA-N 0.000 claims description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 2
- 150000001875 compounds Chemical class 0.000 description 134
- 150000004682 monohydrates Chemical class 0.000 description 42
- 241000486679 Antitype Species 0.000 description 33
- 238000009472 formulation Methods 0.000 description 30
- 230000009466 transformation Effects 0.000 description 29
- 239000000725 suspension Substances 0.000 description 22
- 239000002178 crystalline material Substances 0.000 description 21
- 241000196324 Embryophyta Species 0.000 description 19
- 238000002441 X-ray diffraction Methods 0.000 description 19
- 239000000126 substance Substances 0.000 description 19
- 239000000843 powder Substances 0.000 description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 18
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
- 239000000243 solution Substances 0.000 description 15
- 235000013339 cereals Nutrition 0.000 description 13
- 238000002360 preparation method Methods 0.000 description 13
- 239000000047 product Substances 0.000 description 13
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 12
- 150000001408 amides Chemical class 0.000 description 12
- 238000000113 differential scanning calorimetry Methods 0.000 description 12
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 12
- RLOHOBNEYHBZID-UHFFFAOYSA-N 3-(difluoromethyl)-1-methylpyrazole-4-carboxylic acid Chemical compound CN1C=C(C(O)=O)C(C(F)F)=N1 RLOHOBNEYHBZID-UHFFFAOYSA-N 0.000 description 10
- 238000001237 Raman spectrum Methods 0.000 description 10
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
- 238000001938 differential scanning calorimetry curve Methods 0.000 description 9
- 238000002844 melting Methods 0.000 description 9
- 230000008018 melting Effects 0.000 description 9
- 238000003860 storage Methods 0.000 description 9
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 8
- 239000002904 solvent Substances 0.000 description 8
- 241000209140 Triticum Species 0.000 description 7
- 235000021307 Triticum Nutrition 0.000 description 7
- 244000038559 crop plants Species 0.000 description 7
- 238000002425 crystallisation Methods 0.000 description 7
- 230000008025 crystallization Effects 0.000 description 7
- 239000011159 matrix material Substances 0.000 description 7
- 239000002244 precipitate Substances 0.000 description 7
- XTDZGXBTXBEZDN-UHFFFAOYSA-N 3-(difluoromethyl)-N-(9-isopropyl-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl)-1-methylpyrazole-4-carboxamide Chemical compound CC(C)C1C2CCC1C1=C2C=CC=C1NC(=O)C1=CN(C)N=C1C(F)F XTDZGXBTXBEZDN-UHFFFAOYSA-N 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- 241000233866 Fungi Species 0.000 description 6
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical group CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 6
- 240000008042 Zea mays Species 0.000 description 6
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 6
- 239000006104 solid solution Substances 0.000 description 6
- 235000010469 Glycine max Nutrition 0.000 description 5
- 240000005979 Hordeum vulgare Species 0.000 description 5
- 235000007340 Hordeum vulgare Nutrition 0.000 description 5
- 240000007594 Oryza sativa Species 0.000 description 5
- 235000007164 Oryza sativa Nutrition 0.000 description 5
- 235000007238 Secale cereale Nutrition 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 244000061456 Solanum tuberosum Species 0.000 description 5
- 235000002595 Solanum tuberosum Nutrition 0.000 description 5
- 239000013543 active substance Substances 0.000 description 5
- 239000003905 agrochemical Substances 0.000 description 5
- -1 aliphatic alkyl sulfates Chemical class 0.000 description 5
- 230000008901 benefit Effects 0.000 description 5
- 235000013399 edible fruits Nutrition 0.000 description 5
- 239000000417 fungicide Substances 0.000 description 5
- 239000004615 ingredient Substances 0.000 description 5
- 239000000575 pesticide Substances 0.000 description 5
- 238000000746 purification Methods 0.000 description 5
- 235000009566 rice Nutrition 0.000 description 5
- 239000000741 silica gel Substances 0.000 description 5
- 229910002027 silica gel Inorganic materials 0.000 description 5
- 101100535673 Drosophila melanogaster Syn gene Proteins 0.000 description 4
- 244000068988 Glycine max Species 0.000 description 4
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 4
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 4
- 239000007900 aqueous suspension Substances 0.000 description 4
- 230000008859 change Effects 0.000 description 4
- 235000005822 corn Nutrition 0.000 description 4
- 239000004491 dispersible concentrate Substances 0.000 description 4
- OAYLNYINCPYISS-UHFFFAOYSA-N ethyl acetate;hexane Chemical compound CCCCCC.CCOC(C)=O OAYLNYINCPYISS-UHFFFAOYSA-N 0.000 description 4
- 239000004009 herbicide Substances 0.000 description 4
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 238000000844 transformation Methods 0.000 description 4
- 239000004562 water dispersible granule Substances 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 241000317942 Venturia <ichneumonid wasp> Species 0.000 description 3
- 241000219094 Vitaceae Species 0.000 description 3
- 230000009471 action Effects 0.000 description 3
- 239000012868 active agrochemical ingredient Substances 0.000 description 3
- 239000012141 concentrate Substances 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 238000011161 development Methods 0.000 description 3
- 229910001873 dinitrogen Inorganic materials 0.000 description 3
- 238000004090 dissolution Methods 0.000 description 3
- 235000021021 grapes Nutrition 0.000 description 3
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 229940078552 o-xylene Drugs 0.000 description 3
- 230000005855 radiation Effects 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- 239000007858 starting material Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- 235000013311 vegetables Nutrition 0.000 description 3
- AFABGHUZZDYHJO-UHFFFAOYSA-N 2-Methylpentane Chemical compound CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 2
- KLDLRDSRCMJKGM-UHFFFAOYSA-N 3-[chloro-(2-oxo-1,3-oxazolidin-3-yl)phosphoryl]-1,3-oxazolidin-2-one Chemical compound C1COC(=O)N1P(=O)(Cl)N1CCOC1=O KLDLRDSRCMJKGM-UHFFFAOYSA-N 0.000 description 2
- 241000223600 Alternaria Species 0.000 description 2
- 244000105624 Arachis hypogaea Species 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 2
- 241001480061 Blumeria graminis Species 0.000 description 2
- 101100043727 Caenorhabditis elegans syx-2 gene Proteins 0.000 description 2
- 101100043731 Caenorhabditis elegans syx-3 gene Proteins 0.000 description 2
- 241001157813 Cercospora Species 0.000 description 2
- 240000007154 Coffea arabica Species 0.000 description 2
- 241000371644 Curvularia ravenelii Species 0.000 description 2
- 241000221787 Erysiphe Species 0.000 description 2
- 240000009088 Fragaria x ananassa Species 0.000 description 2
- 241000223218 Fusarium Species 0.000 description 2
- 235000003222 Helianthus annuus Nutrition 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 206010061217 Infestation Diseases 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 240000008415 Lactuca sativa Species 0.000 description 2
- 235000003228 Lactuca sativa Nutrition 0.000 description 2
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 2
- 244000070406 Malus silvestris Species 0.000 description 2
- 241001518729 Monilinia Species 0.000 description 2
- 101100368134 Mus musculus Syn1 gene Proteins 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 241000440444 Phakopsora Species 0.000 description 2
- 241000682843 Pseudocercosporella Species 0.000 description 2
- 241000221300 Puccinia Species 0.000 description 2
- 108020004511 Recombinant DNA Proteins 0.000 description 2
- 241000209056 Secale Species 0.000 description 2
- 241001533598 Septoria Species 0.000 description 2
- 240000003768 Solanum lycopersicum Species 0.000 description 2
- 241000722133 Tilletia Species 0.000 description 2
- 241001154828 Urocystis <tapeworm> Species 0.000 description 2
- 241000221566 Ustilago Species 0.000 description 2
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 230000001154 acute effect Effects 0.000 description 2
- 239000002671 adjuvant Substances 0.000 description 2
- 235000021016 apples Nutrition 0.000 description 2
- 239000008346 aqueous phase Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 235000016213 coffee Nutrition 0.000 description 2
- 235000013353 coffee beverage Nutrition 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000010828 elution Methods 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 235000012055 fruits and vegetables Nutrition 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 238000011065 in-situ storage Methods 0.000 description 2
- 238000002329 infrared spectrum Methods 0.000 description 2
- 239000002917 insecticide Substances 0.000 description 2
- 235000009973 maize Nutrition 0.000 description 2
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 2
- 230000000813 microbial effect Effects 0.000 description 2
- 239000012074 organic phase Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 235000020232 peanut Nutrition 0.000 description 2
- 239000003090 pesticide formulation Substances 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 235000012015 potatoes Nutrition 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 241000894007 species Species 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 235000021012 strawberries Nutrition 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 238000001757 thermogravimetry curve Methods 0.000 description 2
- 239000003053 toxin Substances 0.000 description 2
- 231100000765 toxin Toxicity 0.000 description 2
- 108700012359 toxins Proteins 0.000 description 2
- 238000010626 work up procedure Methods 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- KNZPBAXRJYMFPP-UHFFFAOYSA-N 1-methyl-N-(11-propan-2-yl-3-tricyclo[6.2.1.02,7]undeca-2(7),3,5-trienyl)pyrazole-4-carboxamide Chemical compound CC(C)C1C2CCC1C1=C2C=CC=C1NC(=O)C=1C=NN(C)C=1 KNZPBAXRJYMFPP-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- UPMXNNIRAGDFEH-UHFFFAOYSA-N 3,5-dibromo-4-hydroxybenzonitrile Chemical compound OC1=C(Br)C=C(C#N)C=C1Br UPMXNNIRAGDFEH-UHFFFAOYSA-N 0.000 description 1
- MZGPCLIDFPCPTI-UHFFFAOYSA-N 3-(difluoromethyl)-1-methylpyrazole-4-carbonyl chloride Chemical compound CN1C=C(C(Cl)=O)C(C(F)F)=N1 MZGPCLIDFPCPTI-UHFFFAOYSA-N 0.000 description 1
- UHPMCKVQTMMPCG-UHFFFAOYSA-N 5,8-dihydroxy-2-methoxy-6-methyl-7-(2-oxopropyl)naphthalene-1,4-dione Chemical compound CC1=C(CC(C)=O)C(O)=C2C(=O)C(OC)=CC(=O)C2=C1O UHPMCKVQTMMPCG-UHFFFAOYSA-N 0.000 description 1
- 108010011619 6-Phytase Proteins 0.000 description 1
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 241000919511 Albugo Species 0.000 description 1
- 235000017060 Arachis glabrata Nutrition 0.000 description 1
- 235000010777 Arachis hypogaea Nutrition 0.000 description 1
- 235000018262 Arachis monticola Nutrition 0.000 description 1
- 241000222195 Ascochyta Species 0.000 description 1
- 241000235349 Ascomycota Species 0.000 description 1
- 235000007319 Avena orientalis Nutrition 0.000 description 1
- 241000209763 Avena sativa Species 0.000 description 1
- 235000007558 Avena sp Nutrition 0.000 description 1
- 241000193830 Bacillus <bacterium> Species 0.000 description 1
- 241000221198 Basidiomycota Species 0.000 description 1
- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 1
- 241000190150 Bipolaris sorokiniana Species 0.000 description 1
- 241001465180 Botrytis Species 0.000 description 1
- 241000123650 Botrytis cinerea Species 0.000 description 1
- 240000002791 Brassica napus Species 0.000 description 1
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 1
- 241000233684 Bremia Species 0.000 description 1
- 239000005489 Bromoxynil Substances 0.000 description 1
- GSRIDYWBGNOSLJ-UHFFFAOYSA-N CC(C)C1C2CCC1C1=C2C=CC=C1NC(=O)C1=CN(C)N=C1C Chemical compound CC(C)C1C2CCC1C1=C2C=CC=C1NC(=O)C1=CN(C)N=C1C GSRIDYWBGNOSLJ-UHFFFAOYSA-N 0.000 description 1
- AIEIRXXADOUMAR-UHFFFAOYSA-N CCC(C)CC12C=C3C4C1C3CC24 Chemical compound CCC(C)CC12C=C3C4C1C3CC24 AIEIRXXADOUMAR-UHFFFAOYSA-N 0.000 description 1
- UOIWOHLIGKIYFE-UHFFFAOYSA-N CCCCCNC Chemical compound CCCCCNC UOIWOHLIGKIYFE-UHFFFAOYSA-N 0.000 description 1
- 235000002566 Capsicum Nutrition 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 241000207199 Citrus Species 0.000 description 1
- 241000222199 Colletotrichum Species 0.000 description 1
- 240000008067 Cucumis sativus Species 0.000 description 1
- 235000009849 Cucumis sativus Nutrition 0.000 description 1
- 241000219104 Cucurbitaceae Species 0.000 description 1
- 241001306390 Diaporthe ampelina Species 0.000 description 1
- 101710121765 Endo-1,4-beta-xylanase Proteins 0.000 description 1
- 241000221785 Erysiphales Species 0.000 description 1
- 241000510928 Erysiphe necator Species 0.000 description 1
- 241000223247 Gloeocercospora Species 0.000 description 1
- 241000896246 Golovinomyces cichoracearum Species 0.000 description 1
- 241000219146 Gossypium Species 0.000 description 1
- 241000208818 Helianthus Species 0.000 description 1
- 244000020551 Helianthus annuus Species 0.000 description 1
- 241001181537 Hemileia Species 0.000 description 1
- 241001181532 Hemileia vastatrix Species 0.000 description 1
- 241001330975 Magnaporthe oryzae Species 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 240000005561 Musa balbisiana Species 0.000 description 1
- 235000018290 Musa x paradisiaca Nutrition 0.000 description 1
- 241000131448 Mycosphaerella Species 0.000 description 1
- 244000061176 Nicotiana tabacum Species 0.000 description 1
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 1
- 241001668536 Oculimacula yallundae Species 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 241000233654 Oomycetes Species 0.000 description 1
- 241000736122 Parastagonospora nodorum Species 0.000 description 1
- 241000315044 Passalora arachidicola Species 0.000 description 1
- 241000228143 Penicillium Species 0.000 description 1
- 241001223281 Peronospora Species 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 241000499488 Phragmidium mucronatum Species 0.000 description 1
- 241000210649 Phyllosticta ampelicida Species 0.000 description 1
- 241000233614 Phytophthora Species 0.000 description 1
- 241000758706 Piperaceae Species 0.000 description 1
- 241000233626 Plasmopara Species 0.000 description 1
- 241000896242 Podosphaera Species 0.000 description 1
- 241000317981 Podosphaera fuliginea Species 0.000 description 1
- 241000087479 Pseudocercospora fijiensis Species 0.000 description 1
- 241001281802 Pseudoperonospora Species 0.000 description 1
- 241000228453 Pyrenophora Species 0.000 description 1
- 241000520648 Pyrenophora teres Species 0.000 description 1
- 241000231139 Pyricularia Species 0.000 description 1
- 238000001069 Raman spectroscopy Methods 0.000 description 1
- 241001361634 Rhizoctonia Species 0.000 description 1
- 241001515786 Rhynchosporium Species 0.000 description 1
- 235000004789 Rosa xanthina Nutrition 0.000 description 1
- 241000109329 Rosa xanthina Species 0.000 description 1
- 240000000111 Saccharum officinarum Species 0.000 description 1
- 235000007201 Saccharum officinarum Nutrition 0.000 description 1
- 241000221662 Sclerotinia Species 0.000 description 1
- 241001518640 Sclerotinia homoeocarpa Species 0.000 description 1
- 241000221696 Sclerotinia sclerotiorum Species 0.000 description 1
- 241001597349 Septoria glycines Species 0.000 description 1
- 241001250060 Sphacelotheca Species 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 235000021536 Sugar beet Nutrition 0.000 description 1
- 244000269722 Thea sinensis Species 0.000 description 1
- 241000510929 Uncinula Species 0.000 description 1
- 241000221576 Uromyces Species 0.000 description 1
- 240000006365 Vitis vinifera Species 0.000 description 1
- 235000014787 Vitis vinifera Nutrition 0.000 description 1
- 241001360088 Zymoseptoria tritici Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 230000001775 anti-pathogenic effect Effects 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 235000021028 berry Nutrition 0.000 description 1
- 239000003139 biocide Substances 0.000 description 1
- 238000009395 breeding Methods 0.000 description 1
- 230000001488 breeding effect Effects 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 235000020971 citrus fruits Nutrition 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 238000001640 fractional crystallisation Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000002538 fungal effect Effects 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 238000010353 genetic engineering Methods 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 230000012010 growth Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000002363 herbicidal effect Effects 0.000 description 1
- 238000003898 horticulture Methods 0.000 description 1
- 150000004677 hydrates Chemical class 0.000 description 1
- 239000003262 industrial enzyme Substances 0.000 description 1
- 239000012770 industrial material Substances 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 238000011031 large-scale manufacturing process Methods 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 239000012669 liquid formulation Substances 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 239000003750 molluscacide Substances 0.000 description 1
- 230000002013 molluscicidal effect Effects 0.000 description 1
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 1
- 230000000921 morphogenic effect Effects 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 239000005445 natural material Substances 0.000 description 1
- 239000005645 nematicide Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 230000007918 pathogenicity Effects 0.000 description 1
- 229940085127 phytase Drugs 0.000 description 1
- 230000003032 phytopathogenic effect Effects 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 235000013772 propylene glycol Nutrition 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 description 1
- 235000021251 pulses Nutrition 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000012916 structural analysis Methods 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 239000004546 suspension concentrate Substances 0.000 description 1
- 235000013616 tea Nutrition 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- OUDDUXOVAYIVED-UHFFFAOYSA-N tricyclo[6.2.1.02,7]undeca-2(7),3,5-trien-4-amine Chemical compound C12=CC(N)=CC=C2C2CC1CC2 OUDDUXOVAYIVED-UHFFFAOYSA-N 0.000 description 1
- 238000009369 viticulture Methods 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
110℃〜112℃の単一の融点(ジアステレオマー純度が90%)を有するラセミsyn型の式(I)の化合物の結晶物質が、国際公開第04/35589号(特許文献1)に記載されている。この結晶物質は、ここでは「ラセミsyn型の式(I)の化合物の結晶変態A」と称される。ラセミsyn型の式(I)の化合物の第二の結晶形態は、国際特許出願第PCT/EP2006/00898号明細書中に開示されており、ここでは「ラセミsyn型の式(I)の化合物の結晶変態B」と称される。
上記で説明したように、国際公開第04/35589号には、式(I)の化合物のanti型に富む無定形物質が開示されており、それはanti型とsyn型の比率、65:35を有している。anti型に富む結晶物質は未だ知られていない。
本発明は更にラセミanti型の式(I)の化合物の形態Aの一水和物に関し、この形態は、d間隔および相対強度によって表されるX線粉末回折パターンによって特徴付けられ、このX線粉末回折パターンは、次の特徴的な線を含んでいる:6.39Å(弱)、6.08Å(弱)、5.33Å(強)、4.07Å(弱)、3.84Å(中間)および3.47Å(弱)。このX線粉末回折パターンは、ブルカー(Bruker)−AXS D8アドバンストパウダーエックス線回折計(Advanced Powder X-ray diffractiometer)を用いて、CuKα1を線源として得られてきている。
高純度、例えばラセミsyn型の式(I)の化合物が98質量%以上の純度、を有するラセミsyn型またはanti型の式(I)の化合物の大規模生産は、莫大な費用を伴う。syn型およびanti型の化合物の両方が殺菌性の活性を有しているので、費用と性能を考慮して、両方の化合物を含む混合生成品を生成することが望ましい可能性がある。このような混合生成品は通常はsyn型またはanti型の化合物のいずれかに富んでいる。高度にsyn型に富む混合生成品の例は、80:20〜95:5の範囲のsyn型とanti型の比率を有している。高度にsyn型に富む混合物生成品の他の例は、80:20〜85:15の範囲のsyn型とanti型の比率を有している。
(a)syn型アミドおよびanti型アミドの溶液または懸濁液を調製すること(syn型アミドとanti型アミドの比率は、溶媒もしくは懸濁剤中で、80:20〜95:5の範囲、好ましくは80:20〜90:10の範囲にある)、
(b)以下の形態の種結晶を加えることによって溶媒または懸濁剤から所望の組成物を結晶化させること:
(b1)上記のような結晶変態Cのsyn型アミド、もしくは、
(b2)上記のような結晶変態Cのsyn型アミドおよび上記のようなanti型アミドの形態Aの一水和物の混合物、および
(c)所望の組成物を分離すること、を含んでいる。
a1)分別結晶による純粋なラセミsyn型の式(I)の化合物の調製
240gの結晶の3−ジフルオロメチル−1−メチル−1H−ピラゾール−4−カルボン酸(9−イソプロピル−1,2,3,4−テトラヒドロ−1,4−メタノ−ナフタレン−5−イル)−アミド(純度97.6%、syn型/anti型比が94:6、国際公開第04/35589号または国際公開第06/37632号中に記載されているように、syn型/anti型比が9:1の9−イソプロピル−5−アミノ−ベンゾノルボルネンから出発して調製された)を、560gのメタノールと、温度60℃で混合した。この混合物を65℃に加熱し、そして結晶物質が溶解されるまで攪拌した。この溶液を20分間に亘り、温度40℃まで冷却し、そして次いで2時間に亘って25℃まで冷却した。この時間の間に沈殿が形成された。この沈殿を25℃でろ過し、そして60℃で、真空下に乾燥した。113gの純粋なsyn型の3−ジフルオロメチル−1−メチル−1H−ピラゾール−4−カルボン酸(9−イソプロピル−1,2,3,4−テトラヒドロ−1,4−メタノ−ナフタレン−5−イル)−アミド(純度>99%、融点128℃、収率47%)を得た。この結晶物質を示差走査熱量計およびX線回折によって分析し、そしてsyn型の3−ジフルオロメチル−1−メチル−1H−ピラゾール−4−カルボン酸(9−イソプロピル−1,2,3,4−テトラヒドロ−1,4−メタノ−ナフタレン−5−イル)−アミドの結晶変態Bとして同定し、変態AまたはCの存在は検知されなかった。
syn型に富む5−アミノ−9−イソプロピル−ベンゾノルボルネン(48.83g、syn型/anti型比が9:1、国際公開第04/35589号または国際公開第06/37632号中に記載されているように調製された)をエチルアセテート−ヘキサン(1:6)中のシリカゲル(4.7kg)上でクロマトグラフに掛けた。syn型の含有量が98%超(g.l.c)である最初の溶出画分を合わせて(5.80g)、そしてヘキサンから結晶化してsyn型の含有量が99.8%(g/c)の結晶(4.40g、8.8%、融点が57〜58℃)を得た。5−アミノ−9−syn−イソプロピル−ベンゾノルボルネン(7.32g、99.8%syn型、上記に記載したように調製された)を、5−ジフルオロメチル−2−メチル−ピラゾール−4−カルボン酸(8.33g、1.3当量、国際公開第04/35589号に記載されたように調製された)、ビス−(2−オキソ−3−オキサゾリジニル)−ホスフィン酸クロリド(12.96g、1.4当量)およびトリエチルアミン(9.2g、2.5当量)と、ジクロロメタン(100mL)中で、室温にて、21時間反応させ、飽和NaHCO3溶液での水性の後処理とエチルアセテート−ヘキサン(2:3)中のシリカゲル上での精製の後に、粘調なオイルを得た。ヘキサンからの結晶化で、所望の生成物(12.1g、92.6%、融点128〜130℃、99.2%(g.l.c)のsyn型)を得た。
14mgの、上記のように調製された、純度99%超を有する結晶syn型−3−ジフルオロメチル−1−メチル−1H−ピラゾール−4−カルボン酸(9−イソプロピル−1,2,3,4−テトラヒドロ−1,4−メタノ−ナフタレン−5−イル)−アミドを0.4mLのo−キシレンと混合した。この混合物を結晶物質が溶解されるまで40℃に加熱し、この溶液を40℃に2時間保持した。この溶液を、10℃/時間の冷却速度で5℃まで冷却し、そして次いで5℃で10時間保持した。この時間の間に沈殿が形成された。過剰な溶媒を除去し、そして結晶を窒素ガス流によって乾燥した。syn型の3−ジフルオロメチル−1−メチル−1H−ピラゾール−4−カルボン酸(9−イソプロピル−1,2,3,4−テトラヒドロ−1,4−メタノ−ナフタレン−5−イル)−アミド(純度99%超、融点141℃)が得られた。この結晶物質を示差走査熱量計およびX線回折によって分析し、そしてsyn−3−ジフルオロメチル−1−メチル−1H−ピラゾール−4−カルボン酸(9−イソプロピル−1,2,3,4−テトラヒドロ−1,4−メタノ−ナフタレン−5−イル)−アミドの結晶変態Cとして同定した。変態AまたはBの存在は検知されなかった(図1、2および3を参照)。
anti型に富む5−アミノ−9−イソプロピル−ベンゾノルボルネン(42g、syn型/anti型比が3:7、国際公開第04/35589号または国際公開第06/37632号中に記載されているように調製された)をエチルアセテート−ヘキサン(1:7)中のシリカゲル上でクロマトグラフに掛けた。anti型の含有量が97%超(1.2g、g.l.c)の最後の溶出画分を合わせて、そしてエチルアセテート中のシリカゲル(250g)上で再度クロマトグラフに掛け、anti型の含有量が99.2%(g.l.c)である0.72gの結晶固体(融点が64℃)を得た。
75mgの、上記のように調製された、純度99%超を有する結晶のanti型の3−ジフルオロメチル−1−メチル−1H−ピラゾール−4−カルボン酸(9−イソプロピル−1,2,3,4−テトラヒドロ−1,4−メタノ−ナフタレン−5−イル)−アミドを1mLの水/メタノール(質量比で1:4混合物)と45℃で混合し、そしてこの物質が透明な溶液に溶解されるまで超音波処理した。この溶液を45℃で10時間保持した。この時間の間に沈殿が形成された。過剰な溶媒を除去し、そして結晶を窒素ガス流によって乾燥した。anti型の3−ジフルオロメチル−1−メチル−1H−ピラゾール−4−カルボン酸(9−イソプロピル−1,2,3,4−テトラヒドロ−1,4−メタノ−ナフタレン−5−イル)−アミド(純度99%超)が得られた。この結晶物質を示差走査熱量計およびX線回折によって分析し、そしてanti型の3−ジフルオロメチル−1−メチル−1H−ピラゾール−4−カルボン酸(9−イソプロピル−1,2,3,4−テトラヒドロ−1,4−メタノ−ナフタレン−5−イル)−アミドの形態Aの一水和物として同定した。他の結晶形態の存在は検知されなかった(図7、8および9を参照)。
a)式(I)の化合物の調製
203kgの9−イソプロピル−5−アミノーベンゾノルボルネン(syn型/anti型比が84:16、国際公開第04/35589号または国際公開第06/37632号中に記載されているように調製された、0.42kmol、46%クロロベンゼン溶液)および145kgのクロロベンゼン中の47kgのトリエチルアミン(0.46kmol、1.1当量)の溶液へ、2時間に亘って、201kgの3−ジフルオロメチル−1−メチル1H−ピラゾール−4−カルボニルクロリド(47%クロロベンゼン溶液、0.42kmol、1当量)を40℃で加え、そして15分間攪拌した。水および塩酸の添加(pH6〜7を達成する)後、有機相をクロロベンゼンで抽出した。この有機相を、クロロベンゼンを蒸留することによって濃縮した。次いでメタノール/水(質量比で3:1の混合物)から結晶化した後に、142kgの3−ジフルオロメチル−1−メチル−1H−ピラゾール−4−カルボン酸(9−イソプロピル−1,2,3,4−テトラヒドロ−1,4−メタノ−ナフタレン−5−イル)−アミドが得られた(融点113℃〜114℃、純度93.8%、GCによるsyn型/anti型比が84:16、収率88.6%)。この結晶物質を示差走査熱量計およびX線回折によって分析し、そしてsyn型の3−ジフルオロメチル−1−メチル−1H−ピラゾール−4−カルボン酸(9−イソプロピル−1,2,3,4−テトラヒドロ−1,4−メタノ−ナフタレン−5−イル)−アミドの結晶形態Aとして同定した。他の結晶物質の存在は検知することはできなかった。このデータに基づけば(例えば、独立した結晶のanti型物質は検知されていない)、ラセミanti型の式(I)の化合物は、ラセミsyn型の式(I)の化合物の結晶マトリックス中で固溶体の状態にあると思われる。
上記のP4a)に記載したように調製した2gの結晶物質を12gのメタノール/水(質量比で9:1の混合物)と混合した。この混合物を結晶物質が溶解されるまで50℃に加熱し、この溶液を40℃に2時間攪拌した。この溶液を、15℃/時間の冷却速度で10℃まで冷却した。温度が36℃に到達した時に、0.1gの結晶変態Cのラセミsyn型の式(I)の化合物(上記のP1に記載したように調製された)を加えた。この混合物を10℃に48時間保持した。この時間の間に所望の沈殿が形成された。過剰な溶媒を除去し、そして結晶を窒素ガス流によって乾燥した。結晶物質を得た。
出発物質は、上記のように調製された変態AおよびBのラセミsyn型の式(I)の化合物の混合物である結晶物質であった{上記の実施例P4a)で説明したように、syn型とanti型の比は88:12、純度96%、またこの物質については、anti型の化合物はsyn型の化合物のマトリックス中に固溶体として存在するようである}。
以下の例は本発明を説明するものであり、「活性成分」は式(I)の化合物の新規な固体形態を意味している。
Claims (4)
- d間隔および相対強度によって表されるX線粉末回折パターンが、以下の特徴的な線、13.74Å(強)、7.95Å(弱)、6.94Å(中間)、6.04Å(弱)、4.43Å(中間)および3.72Å(強)を含んでいるX線粉末回折パターンであることを特徴とする、ラセミsyn型の3−ジフルオロメチル−1−メチル−1H−ピラゾール−4−カルボン酸(9−イソプロピル−1,2,3,4−テトラヒドロ−1,4−メタノ−ナフタレン−5−イル)−アミドの結晶変態C。
- 更に示差走査熱量計の温度記録図において130℃〜142℃の範囲にピークを備えた吸熱信号を有することを特徴とする請求項1記載の結晶変態C。
- 植物病原体によって引き起こされる有用な植物またはそれらの繁殖材料の病害の防除用の組成物であって、請求項1に記載のラセミsyn型の3−ジフルオロメチル−1−メチル−1H−ピラゾール−4−カルボン酸(9−イソプロピル−1,2,3,4−テトラヒドロ−1,4−メタノ−ナフタレン−5−イル)−アミドの結晶変態Cを活性成分として、適切な担体とともに殺菌性が有効な量で含む、組成物。
- 植物病原体によって引き起こされる有用な植物またはそれらの繁殖材料の病害を防除する方法であって、有用な植物、それらの場所またはそれらの繁殖材料に、請求項3に記載の組成物を施用することを含む方法。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP07005456.4 | 2007-03-16 | ||
EP07005456 | 2007-03-16 | ||
PCT/EP2008/001259 WO2008113447A2 (en) | 2007-03-16 | 2008-02-19 | Novel solid forms of a microbiocide |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2010521431A JP2010521431A (ja) | 2010-06-24 |
JP5876209B2 true JP5876209B2 (ja) | 2016-03-02 |
Family
ID=39322372
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2009553032A Active JP5876209B2 (ja) | 2007-03-16 | 2008-02-19 | 殺微生物剤の新規な固体形態 |
Country Status (25)
Country | Link |
---|---|
US (1) | US8580835B2 (ja) |
EP (2) | EP2679093A1 (ja) |
JP (1) | JP5876209B2 (ja) |
KR (1) | KR101543705B1 (ja) |
CN (3) | CN101626684B (ja) |
AR (1) | AR065713A1 (ja) |
AU (1) | AU2008228561B2 (ja) |
BR (1) | BRPI0808927B1 (ja) |
CA (1) | CA2679408C (ja) |
CO (1) | CO6220876A2 (ja) |
CR (1) | CR11026A (ja) |
DK (1) | DK2120577T3 (ja) |
EC (1) | ECSP099633A (ja) |
ES (1) | ES2525797T3 (ja) |
GT (1) | GT200900245A (ja) |
HR (1) | HRP20141189T1 (ja) |
IL (1) | IL200048A (ja) |
MX (1) | MX2009009660A (ja) |
PL (1) | PL2120577T3 (ja) |
PT (1) | PT2120577E (ja) |
RU (1) | RU2470921C2 (ja) |
SI (1) | SI2120577T1 (ja) |
UA (1) | UA97267C2 (ja) |
WO (1) | WO2008113447A2 (ja) |
ZA (1) | ZA200905234B (ja) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8563747B2 (en) | 2009-07-31 | 2013-10-22 | Syngenta Crop Protection, Llc | Processes for the alkylation of pyrazoles |
CA2790921A1 (en) * | 2010-02-23 | 2011-09-01 | Nippon Kayaku Co., Ltd. | Stabilized crystal of 2-ethyl-3,7-dimethyl-6-(4-(trifluoromethoxy)phenoxy)quinoline-4-yl methyl carbonate, process for producing the crystal, and agricultural chemical compositioncomprising the crystal |
AR083482A1 (es) | 2010-10-21 | 2013-02-27 | Syngenta Ltd | Concentrados agroquimicos con isopirazam |
GB201403438D0 (en) * | 2014-02-27 | 2014-04-16 | Syngenta Participations Ag | Polymorphs |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0224316D0 (en) * | 2002-10-18 | 2002-11-27 | Syngenta Participations Ag | Chemical compounds |
GB0422401D0 (en) * | 2004-10-08 | 2004-11-10 | Syngenta Participations Ag | Fungicidal compositions |
JP5118043B2 (ja) | 2005-09-16 | 2013-01-16 | シンジェンタ パーティシペーションズ アクチェンゲゼルシャフト | アミドの生成方法 |
-
2008
- 2008-02-19 UA UAA200910377A patent/UA97267C2/ru unknown
- 2008-02-19 RU RU2009138019/04A patent/RU2470921C2/ru active
- 2008-02-19 CA CA2679408A patent/CA2679408C/en active Active
- 2008-02-19 US US12/531,503 patent/US8580835B2/en active Active
- 2008-02-19 AU AU2008228561A patent/AU2008228561B2/en active Active
- 2008-02-19 EP EP13185674.2A patent/EP2679093A1/en not_active Ceased
- 2008-02-19 KR KR1020097019394A patent/KR101543705B1/ko active IP Right Grant
- 2008-02-19 WO PCT/EP2008/001259 patent/WO2008113447A2/en active Application Filing
- 2008-02-19 EP EP08715850.7A patent/EP2120577B1/en active Active
- 2008-02-19 BR BRPI0808927-2A patent/BRPI0808927B1/pt active IP Right Grant
- 2008-02-19 PL PL08715850T patent/PL2120577T3/pl unknown
- 2008-02-19 SI SI200831336T patent/SI2120577T1/sl unknown
- 2008-02-19 ES ES08715850.7T patent/ES2525797T3/es active Active
- 2008-02-19 CN CN2008800072303A patent/CN101626684B/zh active Active
- 2008-02-19 PT PT87158507T patent/PT2120577E/pt unknown
- 2008-02-19 MX MX2009009660A patent/MX2009009660A/es active IP Right Grant
- 2008-02-19 JP JP2009553032A patent/JP5876209B2/ja active Active
- 2008-02-19 CN CN201210449330.XA patent/CN102993098B/zh active Active
- 2008-02-19 DK DK08715850.7T patent/DK2120577T3/en active
- 2008-02-19 CN CN201210448949.9A patent/CN102942526B/zh active Active
- 2008-03-13 AR ARP080101024A patent/AR065713A1/es unknown
-
2009
- 2009-07-23 IL IL200048A patent/IL200048A/en not_active IP Right Cessation
- 2009-07-27 ZA ZA2009/05234A patent/ZA200905234B/en unknown
- 2009-09-10 CO CO09097211A patent/CO6220876A2/es not_active Application Discontinuation
- 2009-09-14 EC EC2009009633A patent/ECSP099633A/es unknown
- 2009-09-14 GT GT200900245A patent/GT200900245A/es unknown
- 2009-09-14 CR CR11026A patent/CR11026A/es unknown
-
2014
- 2014-12-09 HR HRP20141189AT patent/HRP20141189T1/hr unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP2253623B1 (en) | New crystal form of a pyrazole fungicide | |
JP3982879B2 (ja) | 置換カルボン酸アニリド誘導体およびこれを有効成分とする植物病害防除剤 | |
WO2006022225A1 (ja) | 光学活性フタルアミド誘導体及び農園芸用殺虫剤並びにその使用方法 | |
JP5876209B2 (ja) | 殺微生物剤の新規な固体形態 | |
JP2015534940A (ja) | 植物病害防除剤、植物病害防除方法、および植物病害防除用製品 | |
JP2806441B2 (ja) | チオールカルボン酸エステル及びこれを含有する殺菌剤 | |
JPH0463071B2 (ja) | ||
KR20140146222A (ko) | 살균제의 신규한 고체 형태 | |
JP2000103784A (ja) | 5−アルコキシピラゾール−3−カルボキサミド誘導体およびこれを有効成分とする農薬 | |
KR100392075B1 (ko) | 살균효과를 가지는 옥사졸 유도체 | |
CN113788798A (zh) | 氘代的杀菌化合物及其制法和用途 | |
JPH03200774A (ja) | O‐(1,2,4‐トリアゾリル‐1)‐o‐フエニルアセタールおよびそれを含有する殺菌剤 | |
JPH023785B2 (ja) |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20101129 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20130129 |
|
A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20130425 |
|
A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20130507 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20130628 |
|
A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20130917 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20140117 |
|
A911 | Transfer to examiner for re-examination before appeal (zenchi) |
Free format text: JAPANESE INTERMEDIATE CODE: A911 Effective date: 20140128 |
|
A912 | Re-examination (zenchi) completed and case transferred to appeal board |
Free format text: JAPANESE INTERMEDIATE CODE: A912 Effective date: 20140320 |
|
A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20150902 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20151022 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20151120 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20160121 |
|
R150 | Certificate of patent or registration of utility model |
Ref document number: 5876209 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |