JP5511693B2 - 縮合環化した2−ピリドン誘導体及び除草剤 - Google Patents
縮合環化した2−ピリドン誘導体及び除草剤 Download PDFInfo
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- JP5511693B2 JP5511693B2 JP2010549390A JP2010549390A JP5511693B2 JP 5511693 B2 JP5511693 B2 JP 5511693B2 JP 2010549390 A JP2010549390 A JP 2010549390A JP 2010549390 A JP2010549390 A JP 2010549390A JP 5511693 B2 JP5511693 B2 JP 5511693B2
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- alkyl
- alkyl group
- alkoxy
- atom
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- 230000002363 herbicidal effect Effects 0.000 title claims description 40
- 239000004009 herbicide Substances 0.000 title claims description 29
- UBQKCCHYAOITMY-UHFFFAOYSA-N pyridin-2-ol Chemical class OC1=CC=CC=N1 UBQKCCHYAOITMY-UHFFFAOYSA-N 0.000 title claims description 11
- -1 phenyloxy Chemical group 0.000 claims description 512
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 187
- 125000004432 carbon atom Chemical group C* 0.000 claims description 152
- 125000000217 alkyl group Chemical group 0.000 claims description 122
- 125000000623 heterocyclic group Chemical group 0.000 claims description 66
- 229910052757 nitrogen Inorganic materials 0.000 claims description 60
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 55
- 229910052717 sulfur Inorganic materials 0.000 claims description 55
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 51
- 125000005842 heteroatom Chemical group 0.000 claims description 48
- 125000004434 sulfur atom Chemical group 0.000 claims description 46
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 45
- 125000005843 halogen group Chemical group 0.000 claims description 45
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 44
- 125000003545 alkoxy group Chemical group 0.000 claims description 35
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 32
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 31
- 125000003277 amino group Chemical group 0.000 claims description 29
- 229910052799 carbon Inorganic materials 0.000 claims description 29
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims description 28
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 26
- 150000003839 salts Chemical class 0.000 claims description 26
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 25
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims description 24
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims description 24
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 24
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 24
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 22
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 22
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 22
- 125000006771 (C1-C6) haloalkylthio group Chemical group 0.000 claims description 20
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 claims description 19
- 125000005347 halocycloalkyl group Chemical group 0.000 claims description 18
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims description 16
- 125000004749 (C1-C6) haloalkylsulfinyl group Chemical group 0.000 claims description 16
- 125000004741 (C1-C6) haloalkylsulfonyl group Chemical group 0.000 claims description 16
- 125000003118 aryl group Chemical group 0.000 claims description 14
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 13
- 125000004043 oxo group Chemical group O=* 0.000 claims description 12
- 229910052760 oxygen Inorganic materials 0.000 claims description 12
- 239000001301 oxygen Substances 0.000 claims description 12
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 11
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 11
- 239000002689 soil Substances 0.000 claims description 11
- 239000011593 sulfur Chemical group 0.000 claims description 11
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims description 10
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 10
- 125000001424 substituent group Chemical group 0.000 claims description 10
- 125000006823 (C1-C6) acyl group Chemical group 0.000 claims description 9
- 125000004844 (C1-C6) alkoxyimino group Chemical group 0.000 claims description 9
- 239000004480 active ingredient Substances 0.000 claims description 9
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 9
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 9
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 9
- 125000006766 (C2-C6) alkynyloxy group Chemical group 0.000 claims description 8
- 125000006644 (C2-C6) haloalkynyl group Chemical group 0.000 claims description 7
- 125000003320 C2-C6 alkenyloxy group Chemical group 0.000 claims description 7
- 229910052783 alkali metal Inorganic materials 0.000 claims description 7
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 6
- 125000000000 cycloalkoxy group Chemical group 0.000 claims description 6
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 claims description 6
- 125000002837 carbocyclic group Chemical group 0.000 claims description 5
- 125000006539 C12 alkyl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 4
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 claims description 4
- 125000000464 thioxo group Chemical group S=* 0.000 claims description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 3
- 125000004429 atom Chemical group 0.000 claims description 3
- 125000005708 carbonyloxy group Chemical group [*:2]OC([*:1])=O 0.000 claims description 2
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 210
- 150000001875 compounds Chemical class 0.000 description 162
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 132
- 238000004519 manufacturing process Methods 0.000 description 95
- 239000000203 mixture Substances 0.000 description 87
- 239000000243 solution Substances 0.000 description 83
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 77
- 238000006243 chemical reaction Methods 0.000 description 75
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 72
- 239000011541 reaction mixture Substances 0.000 description 71
- 238000005160 1H NMR spectroscopy Methods 0.000 description 70
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 66
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 54
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 53
- 238000002360 preparation method Methods 0.000 description 51
- 239000000543 intermediate Substances 0.000 description 47
- 239000002904 solvent Substances 0.000 description 47
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 45
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 44
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 44
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 43
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 39
- 239000012074 organic phase Substances 0.000 description 37
- 239000007787 solid Substances 0.000 description 37
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 36
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 36
- 239000013078 crystal Substances 0.000 description 32
- 239000002585 base Substances 0.000 description 29
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 27
- 238000004440 column chromatography Methods 0.000 description 25
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 24
- 239000003795 chemical substances by application Substances 0.000 description 24
- 238000000034 method Methods 0.000 description 24
- CTSLXHKWHWQRSH-UHFFFAOYSA-N oxalyl chloride Chemical compound ClC(=O)C(Cl)=O CTSLXHKWHWQRSH-UHFFFAOYSA-N 0.000 description 24
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 24
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 22
- 238000001816 cooling Methods 0.000 description 22
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 22
- 235000017557 sodium bicarbonate Nutrition 0.000 description 22
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 21
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 20
- 239000000706 filtrate Substances 0.000 description 20
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 20
- 241000196324 Embryophyta Species 0.000 description 16
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 16
- HJSLFCCWAKVHIW-UHFFFAOYSA-N cyclohexane-1,3-dione Chemical class O=C1CCCC(=O)C1 HJSLFCCWAKVHIW-UHFFFAOYSA-N 0.000 description 16
- 125000003342 alkenyl group Chemical group 0.000 description 15
- 125000000304 alkynyl group Chemical group 0.000 description 14
- 238000009472 formulation Methods 0.000 description 14
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 description 14
- 150000001721 carbon Chemical group 0.000 description 13
- 125000001188 haloalkyl group Chemical group 0.000 description 13
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 12
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 12
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 12
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 12
- 239000011734 sodium Substances 0.000 description 12
- 229910052708 sodium Inorganic materials 0.000 description 12
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 11
- MWFMGBPGAXYFAR-UHFFFAOYSA-N 2-hydroxy-2-methylpropanenitrile Chemical compound CC(C)(O)C#N MWFMGBPGAXYFAR-UHFFFAOYSA-N 0.000 description 11
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 11
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 11
- 239000008346 aqueous phase Substances 0.000 description 11
- 239000000843 powder Substances 0.000 description 11
- 230000035484 reaction time Effects 0.000 description 11
- 239000000758 substrate Substances 0.000 description 11
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 10
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 10
- 239000002253 acid Substances 0.000 description 10
- 239000000194 fatty acid Substances 0.000 description 10
- 229910000027 potassium carbonate Inorganic materials 0.000 description 10
- 235000011181 potassium carbonates Nutrition 0.000 description 10
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 9
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 9
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 9
- 238000009835 boiling Methods 0.000 description 9
- 235000014113 dietary fatty acids Nutrition 0.000 description 9
- 229930195729 fatty acid Natural products 0.000 description 9
- 239000012442 inert solvent Substances 0.000 description 9
- 239000000126 substance Substances 0.000 description 9
- 235000001508 sulfur Nutrition 0.000 description 9
- 239000004563 wettable powder Substances 0.000 description 9
- LTMRRSWNXVJMBA-UHFFFAOYSA-L 2,2-diethylpropanedioate Chemical compound CCC(CC)(C([O-])=O)C([O-])=O LTMRRSWNXVJMBA-UHFFFAOYSA-L 0.000 description 8
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 8
- 239000000654 additive Substances 0.000 description 8
- 239000003905 agrochemical Substances 0.000 description 8
- 150000001412 amines Chemical class 0.000 description 8
- 125000005129 aryl carbonyl group Chemical group 0.000 description 8
- 229910052751 metal Inorganic materials 0.000 description 8
- 239000002184 metal Substances 0.000 description 8
- 239000000839 emulsion Substances 0.000 description 7
- 239000007788 liquid Substances 0.000 description 7
- 239000012280 lithium aluminium hydride Substances 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- CYPYTURSJDMMMP-WVCUSYJESA-N (1e,4e)-1,5-diphenylpenta-1,4-dien-3-one;palladium Chemical compound [Pd].[Pd].C=1C=CC=CC=1\C=C\C(=O)\C=C\C1=CC=CC=C1.C=1C=CC=CC=1\C=C\C(=O)\C=C\C1=CC=CC=C1.C=1C=CC=CC=1\C=C\C(=O)\C=C\C1=CC=CC=C1 CYPYTURSJDMMMP-WVCUSYJESA-N 0.000 description 6
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 6
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 6
- PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Chemical compound BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 description 6
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 6
- 230000000996 additive effect Effects 0.000 description 6
- 229910052801 chlorine Inorganic materials 0.000 description 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
- 150000002148 esters Chemical class 0.000 description 6
- 230000009969 flowable effect Effects 0.000 description 6
- 239000008187 granular material Substances 0.000 description 6
- 230000002140 halogenating effect Effects 0.000 description 6
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- 239000004094 surface-active agent Substances 0.000 description 6
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 6
- GQHTUMJGOHRCHB-UHFFFAOYSA-N 2,3,4,6,7,8,9,10-octahydropyrimido[1,2-a]azepine Chemical compound C1CCCCN2CCCN=C21 GQHTUMJGOHRCHB-UHFFFAOYSA-N 0.000 description 5
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 5
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical class C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 5
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 5
- 125000004414 alkyl thio group Chemical group 0.000 description 5
- 150000001408 amides Chemical class 0.000 description 5
- 239000012267 brine Substances 0.000 description 5
- 125000001309 chloro group Chemical group Cl* 0.000 description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 5
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 5
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 5
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 5
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 5
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 5
- 239000012312 sodium hydride Substances 0.000 description 5
- 229910000104 sodium hydride Inorganic materials 0.000 description 5
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 5
- 125000004149 thio group Chemical group *S* 0.000 description 5
- 229930192474 thiophene Natural products 0.000 description 5
- 244000045561 useful plants Species 0.000 description 5
- FTNJQNQLEGKTGD-UHFFFAOYSA-N 1,3-benzodioxole Chemical compound C1=CC=C2OCOC2=C1 FTNJQNQLEGKTGD-UHFFFAOYSA-N 0.000 description 4
- HBEDSQVIWPRPAY-UHFFFAOYSA-N 2,3-dihydrobenzofuran Chemical group C1=CC=C2OCCC2=C1 HBEDSQVIWPRPAY-UHFFFAOYSA-N 0.000 description 4
- IBRSSZOHCGUTHI-UHFFFAOYSA-N 2-chloropyridine-3-carboxylic acid Chemical compound OC(=O)C1=CC=CN=C1Cl IBRSSZOHCGUTHI-UHFFFAOYSA-N 0.000 description 4
- BFVQMOCETIVORP-UHFFFAOYSA-N 2-oxo-1h-1,8-naphthyridine-3-carboxylic acid Chemical compound C1=CN=C2NC(=O)C(C(=O)O)=CC2=C1 BFVQMOCETIVORP-UHFFFAOYSA-N 0.000 description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- 241000282472 Canis lupus familiaris Species 0.000 description 4
- 240000003538 Chamaemelum nobile Species 0.000 description 4
- 235000007866 Chamaemelum nobile Nutrition 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- 239000002841 Lewis acid Substances 0.000 description 4
- 235000007232 Matricaria chamomilla Nutrition 0.000 description 4
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 description 4
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 4
- 229920002472 Starch Polymers 0.000 description 4
- 240000008042 Zea mays Species 0.000 description 4
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 4
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 4
- 125000002252 acyl group Chemical group 0.000 description 4
- 125000004644 alkyl sulfinyl group Chemical group 0.000 description 4
- BNBQRQQYDMDJAH-UHFFFAOYSA-N benzodioxan Chemical compound C1=CC=C2OCCOC2=C1 BNBQRQQYDMDJAH-UHFFFAOYSA-N 0.000 description 4
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 4
- FFBHFFJDDLITSX-UHFFFAOYSA-N benzyl N-[2-hydroxy-4-(3-oxomorpholin-4-yl)phenyl]carbamate Chemical compound OC1=C(NC(=O)OCC2=CC=CC=C2)C=CC(=C1)N1CCOCC1=O FFBHFFJDDLITSX-UHFFFAOYSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 235000005822 corn Nutrition 0.000 description 4
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 4
- WQOXQRCZOLPYPM-UHFFFAOYSA-N dimethyl disulfide Chemical compound CSSC WQOXQRCZOLPYPM-UHFFFAOYSA-N 0.000 description 4
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 4
- DNJIEGIFACGWOD-UHFFFAOYSA-N ethanethiol Chemical compound CCS DNJIEGIFACGWOD-UHFFFAOYSA-N 0.000 description 4
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- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 description 1
- 235000019982 sodium hexametaphosphate Nutrition 0.000 description 1
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
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- 235000019832 sodium triphosphate Nutrition 0.000 description 1
- SGUSXTMVKMPQKI-UHFFFAOYSA-M sodium;2,2,3,3-tetrafluoropropanoate Chemical compound [Na+].[O-]C(=O)C(F)(F)C(F)F SGUSXTMVKMPQKI-UHFFFAOYSA-M 0.000 description 1
- JRQGDDUXDKCWRF-UHFFFAOYSA-M sodium;n-(2-methoxycarbonylphenyl)sulfonyl-4-methyl-5-oxo-3-propoxy-1,2,4-triazole-1-carboximidate Chemical compound [Na+].O=C1N(C)C(OCCC)=NN1C(=O)[N-]S(=O)(=O)C1=CC=CC=C1C(=O)OC JRQGDDUXDKCWRF-UHFFFAOYSA-M 0.000 description 1
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- GOLXNESZZPUPJE-UHFFFAOYSA-N spiromesifen Chemical compound CC1=CC(C)=CC(C)=C1C(C(O1)=O)=C(OC(=O)CC(C)(C)C)C11CCCC1 GOLXNESZZPUPJE-UHFFFAOYSA-N 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
- 229940032147 starch Drugs 0.000 description 1
- 229960005322 streptomycin Drugs 0.000 description 1
- 229960004793 sucrose Drugs 0.000 description 1
- NMGNJWORLGLLHQ-UHFFFAOYSA-M sulcofuron-sodium Chemical compound [Na+].[O-]S(=O)(=O)C1=CC(Cl)=CC=C1OC1=CC=C(Cl)C=C1NC(=O)NC1=CC=C(Cl)C(Cl)=C1 NMGNJWORLGLLHQ-UHFFFAOYSA-M 0.000 description 1
- PQTBTIFWAXVEPB-UHFFFAOYSA-N sulcotrione Chemical compound ClC1=CC(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O PQTBTIFWAXVEPB-UHFFFAOYSA-N 0.000 description 1
- OORLZFUTLGXMEF-UHFFFAOYSA-N sulfentrazone Chemical compound O=C1N(C(F)F)C(C)=NN1C1=CC(NS(C)(=O)=O)=C(Cl)C=C1Cl OORLZFUTLGXMEF-UHFFFAOYSA-N 0.000 description 1
- ZDXMLEQEMNLCQG-UHFFFAOYSA-N sulfometuron methyl Chemical group COC(=O)C1=CC=CC=C1S(=O)(=O)NC(=O)NC1=NC(C)=CC(C)=N1 ZDXMLEQEMNLCQG-UHFFFAOYSA-N 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
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- 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
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- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
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- DDVNRFNDOPPVQJ-HQJQHLMTSA-N transfluthrin Chemical compound CC1(C)[C@H](C=C(Cl)Cl)[C@H]1C(=O)OCC1=C(F)C(F)=CC(F)=C1F DDVNRFNDOPPVQJ-HQJQHLMTSA-N 0.000 description 1
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- XOPFESVZMSQIKC-UHFFFAOYSA-N triasulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)OCCCl)=N1 XOPFESVZMSQIKC-UHFFFAOYSA-N 0.000 description 1
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- 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
- YMXOXAPKZDWXLY-QWRGUYRKSA-N tribenuron methyl Chemical group COC(=O)[C@H]1CCCC[C@@H]1S(=O)(=O)NC(=O)N(C)C1=NC(C)=NC(OC)=N1 YMXOXAPKZDWXLY-QWRGUYRKSA-N 0.000 description 1
- REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-N 0.000 description 1
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- BXDAOUXDMHXPDI-UHFFFAOYSA-N trifluoperazine hydrochloride Chemical compound [H+].[H+].[Cl-].[Cl-].C1CN(C)CCN1CCCN1C2=CC(C(F)(F)F)=CC=C2SC2=CC=CC=C21 BXDAOUXDMHXPDI-UHFFFAOYSA-N 0.000 description 1
- 125000005034 trifluormethylthio group Chemical group FC(S*)(F)F 0.000 description 1
- 125000005951 trifluoromethanesulfonyloxy group Chemical group 0.000 description 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 description 1
- ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 description 1
- IMEVJVISCHQJRM-UHFFFAOYSA-N triflusulfuron-methyl Chemical group COC(=O)C1=CC=CC(C)=C1S(=O)(=O)NC(=O)NC1=NC(OCC(F)(F)F)=NC(N(C)C)=N1 IMEVJVISCHQJRM-UHFFFAOYSA-N 0.000 description 1
- 125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 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
- PRXNKYBFWAWBNZ-UHFFFAOYSA-N trimethylphenylammonium tribromide Chemical compound Br[Br-]Br.C[N+](C)(C)C1=CC=CC=C1 PRXNKYBFWAWBNZ-UHFFFAOYSA-N 0.000 description 1
- RVKCCVTVZORVGD-UHFFFAOYSA-N trinexapac-ethyl Chemical group O=C1CC(C(=O)OCC)CC(=O)C1=C(O)C1CC1 RVKCCVTVZORVGD-UHFFFAOYSA-N 0.000 description 1
- NRHFWOJROOQKBK-UHFFFAOYSA-N triphenyltin;hydrate Chemical compound O.C1=CC=CC=C1[Sn](C=1C=CC=CC=1)C1=CC=CC=C1 NRHFWOJROOQKBK-UHFFFAOYSA-N 0.000 description 1
- KVEQCVKVIFQSGC-UHFFFAOYSA-N tritosulfuron Chemical compound FC(F)(F)C1=NC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(F)(F)F)=N1 KVEQCVKVIFQSGC-UHFFFAOYSA-N 0.000 description 1
- YNWVFADWVLCOPU-MAUPQMMJSA-N uniconazole P Chemical compound C1=NC=NN1/C([C@@H](O)C(C)(C)C)=C/C1=CC=C(Cl)C=C1 YNWVFADWVLCOPU-MAUPQMMJSA-N 0.000 description 1
- JARYYMUOCXVXNK-IMTORBKUSA-N validamycin Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-IMTORBKUSA-N 0.000 description 1
- DBXFMOWZRXXBRN-LWKPJOBUSA-N valifenalate Chemical compound CC(C)OC(=O)N[C@@H](C(C)C)C(=O)NC(CC(=O)OC)C1=CC=C(Cl)C=C1 DBXFMOWZRXXBRN-LWKPJOBUSA-N 0.000 description 1
- LESVOLZBIFDZGS-UHFFFAOYSA-N vamidothion Chemical compound CNC(=O)C(C)SCCSP(=O)(OC)OC LESVOLZBIFDZGS-UHFFFAOYSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- WCJYTPVNMWIZCG-UHFFFAOYSA-N xylylcarb Chemical compound CNC(=O)OC1=CC=C(C)C(C)=C1 WCJYTPVNMWIZCG-UHFFFAOYSA-N 0.000 description 1
- 239000005943 zeta-Cypermethrin Substances 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom 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
- C07D215/20—Oxygen atoms
- C07D215/22—Oxygen atoms attached in position 2 or 4
- C07D215/227—Oxygen atoms attached in position 2 or 4 only one oxygen atom which is attached in position 2
-
- 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
- A01N43/34—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
- A01N43/42—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 condensed with carbocyclic rings
-
- 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
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
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- C07D471/04—Ortho-condensed systems
Description
(1) 一般式[I]
X2、X3及びX4は、CH(当該炭素原子はR2により置換されてもよい。);又はN(O)mを表し、
mは、0又は1の整数を表し、
R1は、水素原子;C1〜C12アルキル基;C2〜C6アルケニル基;C2〜C6アルキニル基;C3〜C8シクロアルキル基;C3〜C8シクロアルキルC1〜C6アルキル基;C1〜C6ハロアルキル基;C2〜C6ハロアルケニル基;C2〜C6ハロアルキニル基;C3〜C8ハロシクロアルキル基;C3〜C8ハロシクロアルキルC1〜C6アルキル基;アミノC1〜C6アルキル基;ニトロC1〜C6アルキル基;モノ(C1〜C6アルキル)アミノC1〜C6アルキル基;ジ(C1〜C6アルキル)アミノC1〜C6アルキル基;C1〜C6アルキルチオC1〜C6アルキル基;C1〜C6アルキルスルフィニルC1〜C6アルキル基;C1〜C6アルキルスルホニルC1〜C6アルキル基;C1〜C6ハロアルキルチオC1〜C6アルキル基;C1〜C6ハロアルキルスルフィニルC1〜C6アルキル基;C1〜C6ハロアルキルスルホニルC1〜C6アルキル基;C1〜C6アルコキシC1〜C6アルキル基;ヒドロキシC1〜C6アルキル基;フェニルC1〜C6アルコキシC1〜C6アルキル基(該基のフェニルは、1又は2〜5個の同一もしくは異なるR4により置換されてもよい。);C1〜C6アルコキシC1〜C6アルコキシC1〜C6アルキル基;C3〜C8シクロアルキルオキシC1〜C6アルキル基;C3〜C8シクロアルキルC1〜C6アルコキシC1〜C6アルキル基;フェニルオキシC1〜C6アルキル基(該基のフェニルは、1又は2〜5個の同一もしくは異なるR4により置換されてもよい。);酸素原子、硫黄原子及び窒素原子より選択される1〜5個のヘテロ原子を有する炭素数2〜10の複素環オキシC1〜C6アルキル基(該基の酸素原子、硫黄原子及び窒素原子より選択される1〜5個のヘテロ原子を有する炭素数2〜10の複素環は、1又は2〜5個の同一もしくは異なるR5により置換されてもよい。);フェニルチオC1〜C6アルキル基(該基のフェニルは、1又は2〜5個の同一もしくは異なるR4により置換されてもよい。);フェニルスルフィニルC1〜C6アルキル基(該基のフェニルは、1又は2〜5個の同一もしくは異なるR4により置換されてもよい。);フェニルスルホニルC1〜C6アルキル基(該基のフェニルは、1又は2〜5個の同一もしくは異なるR4により置換されてもよい。);C1〜C6ハロアルコキシC1〜C6アル
キル基;酸素原子、硫黄原子及び窒素原子より選択される1〜5個のヘテロ原子を有する炭素数2〜10の複素環C1〜C6アルコキシC1〜C6アルキル基(該基の酸素原子、硫黄原子及び窒素原子より選択される1〜5個のヘテロ原子を有する炭素数2〜10の複素環は、1又は2〜5個の同一もしくは異なるR5により置換されてもよい。);C1〜C6アルキルチオC1〜C6アルコキシC1〜C6アルキル基;C1〜C6アルキルスルフィニルC1〜C6アルコキシC1〜C6アルキル基;C1〜C6アルキルスルホニルC1〜C6アルコキシC1〜C6アルキル基;シアノC1〜C6アルコキシC1〜C6アルキル基;シアノC1〜C6アルキル基;C1〜C6アルキルカルボニルオキシC1〜C6アルキル基;C1〜C6アシルC1〜C6アルキル基;ジ(C1〜C6アルコキシ)C1〜C6アルキル基;C1〜C6アルコキシカルボニルC1〜C6アルキル基;C1〜C6アルコキシイミノC1〜C6アルキル基;C1〜C6アルキリデンアミノオキシC1〜C6アルキル基;(R6R7N−C=O)C1〜C6アルキル基;C6〜C10アリールC1〜C6アルキル基(該基のアリールは、1又は2〜5個の同一もしくは異なるR4により置換されてもよい。);酸素原子、硫黄原子及び窒素原子より選択される1〜5個のヘテロ原子を有する炭素数2〜10の複素環C1〜C6アルキル基(該基の酸素原子、硫黄原子及び窒素原子より選択される1〜5個のヘテロ原子を有する炭素数2〜10の複素環は、1又は2〜5個の同一もしくは異なるR5により置換されてもよい。);NR8R9基;C1〜C6アルコキシ基;C6〜C10アリール基(該基は1又は2〜5個の同一もしくは異なるR4により置換されてもよい。);又は、酸素原子、硫黄原子及び窒素原子より選択される1〜5個のヘテロ原子を有する炭素数2〜10の複素環基(該基は、1又は2〜5個の同一もしくは異なるR5により置換されてもよい。)を表し、
R2は、ハロゲン原子;ヒドロキシル基;ニトロ基;シアノ基;C1〜C6アルキル基;C3〜C8シクロアルキル基;C3〜C8シクロアルキルC1〜C6アルキル基;C2〜C6アルケニル基;C2〜C6アルキニル基;C1〜C6ハロアルキル基;C2〜C6ハロアルケニル基;C2〜C6ハロアルキニル基;C3〜C8ハロシクロアルキル基;C3〜C8ハロシクロアルキルC1〜C6アルキル基;C1〜C6アルコキシ基;C3〜C8シクロアルキルオキシ基;C3〜C8シクロアルキルC1〜C6アルキルオキシ基;C2〜C6アルケニルオキシ基;C2〜C6アルキニルオキシ基;C1〜C6ハロアルコキシ基;C1〜C6アルコキシC1〜C6アルコキシ基;C1〜C6アルキルカルボニルオキシ基;C1〜C6アルキルチオ基;C1〜C6アルキルスルフィニル基;C1〜C6アルキルスルホニル基;C1〜C6ハロアルキルチオ基;C1〜C6ハロアルキルスルフィニル基;C1〜C6ハロアルキルスルホニル基;アミノ基;モノ(C1〜C6アルキル)アミノ基;ジ(C1〜C6アルキル)アミノ基;C1〜C6アシルアミノ基;ヒドロキシC1〜C6アルキル基;C1〜C6アルコキシC1〜C6アルキル基;C1〜C6アルキルチオC1〜C6アルキル基;C1〜C6アルキルスルフィニルC1〜C6アルキル基;C1〜C6アルキルスルホニルC1〜C6アルキル基;C1〜C6ハロアルキルチオC1〜C6アルキル基;C1〜C6ハロアルキルスルフィニルC1〜C6アルキル基;C1〜C6ハロアルキルスルホニルC1〜C6アルキル基;シアノC1〜C6アルキル基;C1〜C6アシル基;C1〜C6アルコキシイミノC1〜C6アルキル基;カルボキシル基;C1〜C6アルコキシカルボニル基;カルバモイル基;モノ(C1〜C6アルキル)アミノカルボニル基;ジ(C1〜C6アルキル)アミノカルボニル基;又は、酸素原子、硫黄原子及び窒素原子より選択される1〜5個のヘテロ原子を有する炭素数2〜10の複素環基(該基の酸素原子、硫黄原子及び窒素原子より選択される1〜5個のヘテロ原子を有する炭素数2〜10の複素環は、1又は2〜5個の同一もしくは異なるR10により置換されてもよい。)を表し、
また、R2は、隣接した2個のR2が一緒になって、それぞれのR2が直接結合している炭素原子と共に、炭素環又は酸素原子、硫黄原子及び窒素原子より選択される1〜4個のヘテロ原子を有する複素環である4〜8員環を形成してもよく、このときに形成された環はハロゲン原子;シアノ基;ニトロ基;C1〜C6アルキル基;C1〜C6ハロアルキル基;C1〜C6アルコキシ基;C1〜C6ハロアルコキシ基;又はオキソ基で置換されてもよく、
nは、X2、X3及びX4がCH(該炭素原子はR2により置換されてもよい。)、即ち、置換基R2により置換されてもよいCHである場合は0〜4の整数を表し、
R3は、ヒドロキシル基;O−M+(M+はアルカリ金属カチオン又はアンモニウムカチオンを示す。);アミノ基;ハロゲン原子;C1〜C6アルキルスルホニルオキシ基;C1〜C6アルキルチオ基;C1〜C6アルキルスルフィニル基;C1〜C6アルキルスルホニル基;C1〜C6ハロアルキルチオ基;C1〜C6ハロアルキルスルフィニル基;C1〜C6ハロアルキルスルホニル基;C2〜C6アルケニルチオ基;C2〜C6アルケニルスルフィニル基;C2〜C6アルケニルスルホニル基;C2〜C6アルキニルチオ基;C2〜C6アルキニルスルフィニル基;C2〜C6アルキニルスルホニル基;C1〜C6アルキルカルボニルオキシ基;C2〜C6アルケニルカルボニルオキシ基;C2〜C6アルキニルカルボニルオキシ基;フェノキシ基(該基は、1又は2〜5個の同一もしくは異なるR10により置換されてもよい。);フェニルチオ基(該基は、1又は2〜5個の同一もしくは異なるR10により置換されてもよい。);フェニルスルフィニル基(該基は、1又は2〜5個の同一もしくは異なるR10により置換されてもよい。);フェニルスルホニル基(該基は、1又は2〜5個の同一もしくは異なるR10により置換されてもよい。);フェニルスルホニルオキシ基(該基は、1又は2〜5個の同一もしくは異なるR10により置換されてもよい。);フェニルカルボニルオキシ基(該基は、1又は2〜5個の同一もしくは異なるR10により置換されてもよい。);1,2,4−トリアゾール−1−イル基;1,2,3−トリアゾール−1−イル基;1,2,3−トリアゾール−2−イル基;イミダゾール−1−イル基;ピラゾール−1−イル基;テトラゾール−1−イル基;又はテトラゾール−2−イル基を表し、
R4は、ハロゲン原子;ヒドロキシル基;ニトロ基;シアノ基;C1〜C6アルキル基;C3〜C8シクロアルキル基;C3〜C8シクロアルキルC1〜C6アルキル基;C2〜C6アルケニル基;C2〜C6アルキニル基;C1〜C6ハロアルキル基;C2〜C6ハロアルケニル基;C2〜C6ハロアルキニル基;C3〜C8ハロシクロアルキル基;C3〜C8ハロシクロアルキルC1〜C6アルキル基;C1〜C6アルコキシ基;C3〜C8シクロアルキルオキシ基;C2〜C6アルケニルオキシ基;C2〜C6アルキニルオキシ基;C1〜C6アルキルカルボニルオキシ基;C1〜C6ハロアルコキシ基;C1〜C6アルキルチオ基;C1〜C6アルキルスルフィニル基;C1〜C6アルキルスルホニル基;C1〜C6ハロアルキルチオ基;C1〜C6ハロアルキルスルフィニル基;C1〜C6ハロアルキルスルホニル基;アミノ基;C1〜C6アシルアミノ基;モノ(C1〜C6アルキル)アミノ基;ジ(C1〜C6アルキル)アミノ基;ヒドロキシC1〜C6アルキル基;C1〜C6アルコキシC1〜C6アルキル基;C1〜C6アルキルチオC1〜C6アルキル基;C1〜C6アルキルスルフィニルC1〜C6アルキル基;C1〜C6アルキルスルホニルC1〜C6アルキル基;C1〜C6ハロアルキルチオC1〜C6アルキル基;C1〜C6ハロアルキルスルフィニルC1〜C6アルキル基;C1〜C6ハロアルキルスルホニルC1〜C6アルキル基;シアノC1〜C6アルキル基;C1〜C6アルコキシC1〜C6アルコキシ基;C3〜C8シクロアルキルC1〜C6アルキルオキシ基;C1〜C6ハロアルコキシC1〜C6アルコキシ基;シアノC1〜C6アルコキシ基;C1〜C6アシル基;C1〜C6アルコキシイミノC1〜C6アルキル基;カルボキシル基;C1〜C6アルコキシカルボニル基;カルバモイル基;モノ(C1〜C6アルキル)アミノカルボニル基;ジ(C1〜C6アルキル)アミノカルボニル基;酸素原子、硫黄原子及び窒素原子より選択される1〜5個のヘテロ原子を有する炭素数2〜10の複素環基(該基の複素環は、1又は2〜5個の同一もしくは異なるR10により置換されてもよい。);又は、酸素原子、硫黄原子及び窒素原子より任意に選択される1〜5個のヘテロ原子を有する炭素数2〜10の複素環オキシ基(該基の酸素原子、硫黄原子及び窒素原子より選択さ
れる1〜5個のヘテロ原子を有する炭素数2〜10の複素環は、1又は2〜5個の同一もしくは異なるR10により置換されてもよい。)を表し、
また、R4は、隣接した2個のR4が一緒になって、それぞれのR4が直接結合している炭素原子と共に、炭素環又は酸素原子、硫黄原子及び窒素原子より選択される1〜4個のヘテロ原子を有する複素環である4〜8員環を形成してもよく、このときに形成された環はハロゲン原子;シアノ基;ニトロ基;C1〜C6アルキル基;C1〜C6ハロアルキル基;C1〜C6アルコキシ基;C1〜C6ハロアルコキシ基;又はオキソ基で置換されてもよく、
R5は、オキソ基;チオキソ基;ヒドロキシル基;ハロゲン原子;ニトロ基;シアノ基;C1〜C6アルキル基;C2〜C6アルケニル基;C2〜C6アルキニル基;C3〜C8シクロアルキル基;C3〜C8シクロアルキルC1〜C6アルキル基;C1〜C6ハロアルキル基;C2〜C6ハロアルケニル基;C3〜C8ハロシクロアルキル基;C3〜C8ハロシクロアルキルC1〜C6アルキル基;C1〜C6アルコキシ基;C2〜C6アルケニルオキシ基;C2〜C6アルキニルオキシ基;C3〜C8シクロアルキルオキシ基;C3〜C8シクロアルキルC1〜C6アルキルオキシ基;C1〜C6ハロアルコキシ基;C1〜C6アルコキシC1〜C6アルコキシ基;C1〜C6ハロアルコキシC1〜C6アルコキシ基;シアノC1〜C6アルコキシ基;C1〜C6アルキルカルボニルオキシ基;C1〜C6アルキルチオ基;C1〜C6アルキルスルフィニル基;C1〜C6アルキルスルホニル基;C1〜C6ハロアルキルチオ基;C1〜C6ハロアルキルスルフィニル基;C1〜C6ハロアルキルスルホニル基;アミノ基;モノ(C1〜C6アルキル)アミノ基;ジ(C1〜C6アルキル)アミノ基;C1〜C6アシルアミノ基;カルボキシル基;C1〜C6アルコキシカルボニル基;カルバモイル基;モノ(C1〜C6アルキル)アミノカルボニル基;ジ(C1〜C6アルキル)アミノカルボニル基;C1〜C6アシル基;C1〜C6アルコキシイミノC1〜C6アルキル基;C1〜C6アルコキシC1〜C6アルキル基;C1〜C6アルキルチオC1〜C6アルキル基;C1〜C6アルキルスルフィニルC1〜C6アルキル基;C1〜C6アルキルスルホニルC1〜C6アルキル基;C1〜C6ハロアルキルチオC1〜C6アルキル基;C1〜C6ハロアルキルスルフィニルC1〜C6アルキル基;C1〜C6ハロアルキルスルホニルC1〜C6アルキル基;又はシアノC1〜C6アルキル基を表し、
また、R5は、隣接した2個のR5が一緒になって、それぞれのR5が直接結合している炭素原子と共に、炭素環又は酸素原子、硫黄原子及び窒素原子より選択される1〜4個のヘテロ原子を有する複素環である4〜8員環を形成してもよく、このときに形成された環はハロゲン原子;シアノ基;ニトロ基;C1〜C6アルキル基;C1〜C6ハロアルキル基;C1〜C6アルコキシ基;C1〜C6ハロアルコキシ基;又はオキソ基で置換されてもよく、
R6及びR7は、互いに独立して、C1〜C6アルキル基;又はフェニルC1〜C6アルキルオキシカルボニル基を表し、
また、R6及びR7は、これらが一緒になってこれらが結合している窒素原子と共に5〜6員環を形成していてもよく、このときに形成された環中にR6及びR7が結合している窒素原子以外に酸素原子が介在していてもよく、
R8及びR9は、互いに独立して、水素原子;C1〜C6アルキル基;NR6R7基;又はC1〜C6アルコキシカルボニル基を表し、
また、R8及びR9は、これらが一緒になってこれらが結合している窒素原子と共に5〜6員環を形成していてもよく、この際、この環中にR8及びR9が結合している窒素原子以外に硫黄原子及び/又は酸素原子が介在していてもよく、
R10は、ハロゲン原子;ニトロ基;シアノ基;C1〜C6アルキル基;C1〜C6ハロアルキル基;C1〜C6アルコキシ基;又はC1〜C6ハロアルコキシ基を表し、
A1は、C(R11R12)を表し、
A2は、C(R13R14)、又はC=Oを表し、
A3は、C(R15R16)を表し、
R11、R12、R13、R14、R15及びR16は、互いに独立して、水素原子;又はC1〜C6アルキル基を表し、
また、R11とR16はこれらが一緒になってC2〜C5アルキレン鎖を形成し、隣接する炭素原子と共に環を構成しても良い。}
で表される2−ピリドン誘導体又はその農薬上許容される塩。
(2) 前記(1)に記載の2−ピリドン誘導体又はその塩を活性成分として含有することを特徴とする除草剤。
(3) 前記(2)に記載の除草剤の有効量を土壌及び/又は植物に処理することを特徴とする除草剤の使用。
(4) 前記(2)に記載の除草剤の有効量を土壌及び/又は植物に処理することを特徴とする除草方法。
また、アルキル基、アルケニル基などの炭素鎖による基の命名においては、特に指定がない場合には、ノルマル(n−)であることを示す。
フェニルC1〜C6アルキルオキシカルボニル基とは、特に限定しない限り、アルキル部分が上記の意味である、フェニルにより置換された炭素数が1〜6の(アルキル)−O−CO−基を示し、例えばベンジルオキシカルボニル又はフェネチルオキシカルボニル等の基を挙げることができる。
アルカリ金属としては、ナトリウム、カリウム等が好ましい。
さらに、好ましいR1としては、C1〜C12アルキル基、C2〜C6アルケニル基、C2〜C6アルキニル基、C3〜C8シクロアルキル基、C1〜C6ハロアルキル基、C2〜C6ハロアルケニル基、C1〜C6アルキルチオC1〜C6アルキル基、C1〜C6アルキルスルホニルC1〜C6アルキル基、C1〜C6アルコキシC1〜C6アルキル基、C1〜C6アルコキシC1〜C6アルコキシC1〜C6アルキル基、C1〜C6ハロアルコキシC1〜C6アルキル基、テトラヒドロフラニルC1〜C6アルコキシC1〜C6アルキル基、シアノC1〜C6アルキル基、C1〜C6アルコキシカルボニルC1〜C6アルキル基、C6〜C10アリールC1〜C6アルキル基(該基のアリールは、1又は2個以上の同一又は異なるR4により置換されてもよい。)、複素環C1〜C6アルキル基(該基は、1又は2個以上の同一又は異なるR5により置換されてもよい。)、C6〜C10アリール基(該基は、1又は2個以上の同一又は異なるR4により置換されてもよい。)、又は複素環基(該基は、1又は2個以上の同一又は異なるR5により置換されてもよい)などが挙げられる。
より好ましいR4としては、ハロゲン原子;C1〜C6アルキル基;C1〜C6ハロアルキル基;C1〜C6アルコキシ基;C2〜C6アルケニルオキシ基;C2〜C6アルキニルオキシ基;C1〜C6ハロアルコキシ基;又はC1〜C6アシル基などが挙げられる。
さらに好ましいR4としては、ハロゲン原子;C1〜C6アルキル基;C1〜C6ハロアルキル基;C1〜C6アルコキシ基;又はC1〜C6ハロアルコキシ基などが挙げられる。
また、R4は、隣接した2個のR4が一緒になって、それぞれのR4が直接結合している炭素原子と共に、炭素環、又は酸素原子、硫黄原子及び窒素原子より選択される1〜4個のヘテロ原子を有する複素環である4〜8員環を形成することも好ましい。
このような炭素環又は複素環の好ましい例としては次の構造式で示されるものが挙げられる。
より好ましいR5としては、ハロゲン原子;C1〜C6アルキル基;又はC1〜C6ハロアルキル基などがあげられる。
−C(R11R12)−C(R13R14)−C(R15R16)−、又は、
−C(R11R12)−C(=O)−C(R15R16)−
を表し、これらが隣接する炭素原子と共に6員の炭素環を形成する。
例えば、
Meとはメチル基を示し、
Etとはエチル基を示し、
n−Prとはn−プロピル基を示し、
i−Prとはイソプロピル基を示し、
c−Prとはシクロプロピル基を示し、
n−Buとはn−ブチル基を示し、
s−Buとはsec−ブチル基を示し、
i−Buとはイソブチル基を示し、
t−Buとはtert−ブチル基を示し、
c−Buとはシクロブチル基を示し、
n−Penとはn−ペンチル基を示し、
c−Penとはシクロペンチル基を示し、
n−Hexとはn−ヘキシル基を示し、
Phとはフェニル基を示し、
Bnとはベンジル基を示し、
R2及びR12において「−」とはそれらが無置換であることを示し、
(4−Cl)Bnとは4−クロロベンジル基を示し、
3,4−(CH2CH2CH2CH2)−とは、3位と4位が当該ブチレン基で結合されて環を形成した次の化学構造、
3,4−(OCH2CH2O)−とは、同様に3位と4位が当該エチレンジオキシ基で結合されて環を形成した次の化学構造、
次の一般式[1a]で示される本発明化合物は下記に例示する反応式からなる方法により製造することができる。
(工程1)
一般式[2]で表される化合物と式[3a]で表される化合物とを、溶媒中、塩基の存在下で反応させることにより、一般式[4a]及び[4b]で表されるエノールエステル化合物を製造することができる。
(以下、例えば「一般式[2]で表される化合物」のことを、単に「式[2]」と略記することがある。)
ここで使用する式[3a]の使用量は、式[2]1モルに対して0.5〜10モルの範囲から適宜選択すればよく、好ましくは1.0〜1.2モルである。
式[4a]及び[4b]は、式[2]と式[3b]とを、塩基の存在下又は非存在下、脱水縮合剤存在下、溶媒中で反応させることによっても製造することができる。
式[1a]は、前記工程1又は2で製造された式[4a]及び式[4b]とシアノ化合物とを塩基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。
式[1a]の化合物は、式[2]と式[3c]とを、溶媒中、塩基又はルイス酸存在下で反応させることによっても製造することができる。
シアノ化剤としては、アルカリ金属シアン化物、アルカリ土類金属シアン化物が用いられる。
シアノ化剤の使用量は化合物[3a−1]1モルに対して0.5〜10モルの範囲から適宜選択すればよく、好ましくは0.9〜1.1モルである。
さらに、前記した本発明の式[1a]で表される化合物から、以下の製造方法によって本発明の式[1b]及び[1c]で表される化合物を製造することができる。
すなわち、式[1a]の化合物とハロゲン化剤とを、溶媒中で反応させることにより、式[1b]の化合物を製造し、さらに式[1b]の化合物と求核試薬とを、溶媒中、塩基の存在下で反応させることにより式[1c]の化合物を製造することができる。
また、次の一般式[1d]で示される本発明化合物は下記に例示する反応式からなる方法により製造することができる。
本発明化合物の製造中間体である式[3a−1]は、式[3b]とハロゲン化剤とを溶媒中又は無溶媒中で反応させることによって製造することができる。)
本反応で使用できるハロゲン化剤としては、例えば塩化オキザリル、塩化チオニル等があげられる。
式[3b]の製造中間体は、式[3d]を溶媒中、酸存在下又は塩基存在下で加水分解させることにより製造することができる。
式[3d−1]の製造中間体は、式[3e]と式[5]とを、塩基存在下又は非存在下で、溶媒中又は無溶媒で反応させることにより製造することができる。
〈中間体製造法4〉
式[3d−2]の製造中間体は、テトラヘドロン(Tetrahedron)、第55巻、第12757−12770頁(1999年)に記載の方法に準じ、式[3e]と式[6]とを銅触媒及び塩基存在下で反応させることにより製造することができる。
式[3d−3]の製造中間体は、米国特許公開US2005/256000号公報に記載の方法に準じ、式[3d−4]で表される化合物とローソン試薬(Lawesson's Reagent)とを反応させることにより製造することができる。
式[3d−1]の製造中間体は、米国特許US6562811号公報、国際特許WO2007/53131号公報、ジャーナル・オブ・ザ・オーガニック・ケミストリー(Journal of the Organic Chemistry)第58巻、第6625−6628頁(1993年)の方法に準じ、式[7]と式[8]で表されるマロン酸ジエステルとを反応させることにより製造することができる。
式[7]は、実験化学講座第4版(丸善)、第23巻、21頁の「活性二酸化マンガンによる酸化の項」に準じて、式[9]で表されるアルコール化合物を酸化することにより製造することができる。
〈中間体製造法8〉
式[9]の製造中間体は、WO2004/20414号公報、米国特許公開US2008/176827号公報、ジャーナル・オブ・メディシナル・ケミストリー(Journal of Medicinal Chemistry)、第31巻、第2108−2121頁(1988年)及びジャーナル・オブ・メディシナル・ケミストリー(Journal of Medicinal Chemistry)、第48巻、第12号、第4100−4110頁(2005年)等に記載の方法に準じ、式[10]とR1−NH2とを反応させることにより製造することができる。
式[3e]の製造中間体は、上記に示す工程で製造することができる。
式[3d−7]の製造中間体は、上記に示す工程で製造することができる。
式[3d−9]の製造中間体は、WO2005/26123号公報、テトラヘドロン(Tetrahedron)、第40巻、第2985項(1984年)及びシンセシス・コミュニケーションズ(Synthetic Communications)、第18巻、第1171項(1988年)等に記載の方法に準じて、式[3d−8]と式[16]とを反応させることにより製造することができる。
メトリン(desmetryne)、テブタム(tebutam)、ナプロアニリド(naproanilide)、バーナレート(vernolate)、フェニュロン(fenuron)、フルアゾレート(fluazolate)、プロフルアゾール(profluazol)、メトブロムロン(metobromuron)、メトベンズロン(metobenzuron)、AE−F−150944(コード番号)SYP−298(コード番号)SYP−300(コード番号)HOK−201(コード番号)NC−620(コード番号)1−ナフチルアセトアミド(α-naphthalene acetamide)、1−メチルシクロプロペン(1-methylcyclopropene)、2,6‐ジイソプロピルナフタレン(2,6-diisopropylnaphthalene)、4−CPA、アビグリシン(aviglycine)、アンシミドール(ancymidol)、イナベンフィド(inabenfide)、インドール酢酸(indole acetic acid)、インドール酪酸(indole butyric acid)、ウニコナゾール(uniconazole)、ウニコナゾール・P(uniconazole-P)、エチクロゼート(ethychlozate)、エテホン(ethephon)、カルボネ(carvone)、クロキシホナック(cloxyfonac-sodium)、クロキシホナック・カリウム塩(cloxyfonac-potassium)、クロプロップ(cloprop)、クロルメコート(chlormequat)、サイトカイニン(cytokinins)、シクラニリド(cyclanilide)、ジケグラック(dikegulac)、ジベレリン(gibberellic acid)、ジメチピン(dimethipin)、シントフェン(sintofen)、ダミノジット(daminozide)、チジアズロン(thidiazuron)、デシルアルコール(n-decanol)、トリアコンタノール(1-triacontanol)、トリネキサパック・エチル(trinexapac-ethyl)、パクロブトラゾール(paclobutrazol)、フルメトラリン(flumetralin)、フルルプリミドール(flurprimidol)、フルレノール(flurenol)、プロヒドロジャスモン(prohydrojasmon),プロヘキサジオン・カルシウム塩(prohexadione-calcium)、ベンジルアミノプリン((6-)benzylaminopurine)、ホルクロルフェニュロン(forchlorfenuron)、マレイン酸ヒドラジド(maleic hydrazide)、メピコート・クロリド(mepiquat)、メフルイジド(mefluidide)、メプチルジノカップ(meptyldinocap)、インダジフラム(indaziflam)、プロピリスルフロン(propyrisulfuron)、メチオゾリン(methiozolin)、xazasulfuron(dioxasulfuron)、ビシクロピロン(bicyclopyrone)、メタゾスルフロン(metazosulfuron)、heptamaloxyloglucan、EL101GV(コード番号)、ジメチルジスルフィド及び次の式[C]
1−メチル−2−オキソ−1,2−ジヒドロキノリン−3−カルボン酸0.76g(3.7mmol)をジクロロメタン(50mL)に溶解し、塩化オキザリル1.0mL(12mmol)を加えた。この混合物にN,N−ジメチルホルムアミド2滴を加えて40℃で1時間攪拌した。この反応溶液を減圧下濃縮し、1−メチル−2−オキソ−1,2−ジヒドロキノリン−3−カルボン酸クロリドを得た。得られた酸クロリドをアセトニトリル(30mL)に溶解し、この溶液を1,3−シクロヘキサンジオン0.46g(4.1mmol)とトリエチルアミン0.63mL(4.5mmol)のアセトニトリル(50mL)溶液に氷冷下で添加し、室温で1晩撹拌した。この反応混合物を、水にあけ、酢酸エチルで抽出し、有機相を水、炭酸水素ナトリウム水溶液、水の順で洗浄後、乾燥、濃縮した。残渣をカラムクロマトグラフィー(酢酸エチル:n‐ヘキサン=1:4〜1:0)で精製し、淡黄色粉末の標記化合物を0.48g(収率43%)得た。
2.10-2.16(2H,m)、2.47(2H,t)、2.73(2H,t)、3.77(3H,s)、6.04(1H,s)、7.32(1H,t)、7.40(1H,d)、7.70-7.75(1H,m)、8.53(1H,s)
3−オキソ−1−シクロヘキセニル 1−メチル−2−オキソ−1,2−ジヒドロキノリン−3−カルボキシレート0.48g(1.6mmol)をアセトニトリル(40mL)に溶解し、この溶液にトリエチルアミン0.25mL(1.8mmol)とアセトンシアノヒドリン0.15g(1.8mmol)を加え、室温で一昼夜撹拌した。反応混合物を飽和重曹水にあけ、酢酸エチルで洗浄した。水相にクエン酸を加えてpH3〜4とし、酢酸エチルで抽出し、有機相を水洗、乾燥、濃縮した。残渣にジイソプロピルエーテルを加えて結晶化させ、さらに結晶をジイソプロピルエーテルで洗浄して黄色粉末の標記化合物を0.24g(収率50%)得た。
2.03-2.11(2H,m)、2.49(2H,t)、2.74(2H,t)、3.70(3H,s)、7.24 (1H,t)、7.36(1H,d)、7.58-7.62(1H,m)、7.77(1H,s)、16.6(1H,s)
1−メチル−2−オキソ−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボン酸1.0g(4.9mmol)をジクロロメタン(50mL)に溶解し、塩化オキザリル1.0mL(12mmol)を加えた。この混合物にN,N−ジメチルホルムアミド3滴を加えて40℃で1時間攪拌した。反応溶液を減圧下濃縮し、1−メチル−2−オキソ−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボン酸クロリドを得た。得られた酸クロリドをアセトニトリル(30mL)に溶解し、この溶液を1,3−シクロヘキサンジオン0.60g(5.4mmol)とトリエチルアミン0.82mL(5.9mmol)のアセトニトリル(50mL)溶液に氷冷下で添加し、室温で1時間攪拌した。反応混合物を、水にあけ、酢酸エチルで抽出し、有機相を水、炭酸水素ナトリウム水溶液、水の順で洗浄後、乾燥、濃縮した。残渣をジイソプロピルエーテルで洗浄して微黄色固体の標記化合物を0.83g得た(収率57%)。
2.09 -2.18(2H,m)、2.47(2H,t)、2.73(2H,t)、3.89(3H,s)、6.05(1H,s)、7.25-7.29(1H,m)、8.03(1H,dd)、8.49(1H,s) 、8.75(1H,dd)
3−オキソ−1−シクロヘキセニル 1−メチル−2−オキソ−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボキシレート0.83g(2.8mmol)をアセトニトリル(50mL)に溶解した。この溶液にトリエチルアミン0.43mL(3.1mmol)とアセトンシアノヒドリン0.26g(3.1mmol)を加え、室温で一昼夜撹拌した。反応混合物を飽和重曹水にあけ、酢酸エチルで洗浄し、水相にクエン酸を加えてpH3〜4としてから酢酸エチルで抽出した。有機相を水洗、乾燥、濃縮し、残渣をカラムクロマトグラフィー(酢酸エチル:n‐ヘキサン=1:1〜1:0)で精製し淡黄色粉末の標記化合物を0.30g得た(収率36%)。
2.03-2.12(2H,m)、2.49(2H,t)、2.75(2H,t)、3.92(3H,s)、7.17-7.21(1H,m)、7.69(1H,s) 、7.91(1H,dd)、8.63(1H,dd)、16.5(1H,s)
1−(エチルチオメチル)−2−オキソ−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボン酸2.20g(8.3mmol)をジクロロメタン(80mL)に溶解し、塩化オキザリル5.0mL(60mmol)を加えた。この混合物にN,N−ジメチルホルムアミド1滴を加えて室温で1時間攪拌した。反応溶液を減圧下濃縮し、1−(エチルチオメチル)−2−オキソ−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボン酸クロリドを得た。得られた酸クロリドをジクロロメタン(80mL)に溶解し、この溶液に1,3−シクロヘキサンジオン1.02g(9.1mmol)とトリエチルアミン1.40mL(10.0mmol)を氷冷下で添加し、室温で2時間攪拌した。反応混合物を、炭酸水素ナトリウム水溶液にあけ、ジクロロメタンで抽出し、有機相を乾燥、濃縮した。残渣をジイソプロピルエーテルで洗浄して微黄色固体の標記化合物を2.99g得た(収率 定量的)。
1.32(3H,t)、2.10-2.16(2H,m)、2.47(2H,t)、2.72(2H,t)、2.84(2H,q)、5.68(2H,s)、6.04(1H,s)、7.28-7.31(1H,m)、8.03(1H,d)、8.50(1H,s)、8.75(1H,d)
3−オキソ−1−シクロヘキセニル 1−(エチルチオメチル)−2−オキソ−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボキシレート2.97g(8.3mmol)をジクロロメタン(80mL)に溶解した。この溶液にトリエチルアミン1.40mL(10.0mmol)とアセトンシアンヒドリン0.77g(9.1mmol)を加え、室温で一晩撹拌した。反応混合物をクエン酸水溶液にあけ、ジクロロメタンで抽出し、有機相を水洗、乾燥、濃縮した。残渣をカラムクロマトグラフィー(酢酸エチル:n‐ヘキサン=1:4)で精製し、淡橙色結晶の標記化合物を0.77g得た(収率26%)。
1.29(3H,t)、2.05-2.12(2H,m)、2.47(2H,t)、2.73-2.82(4H,m)、5.63(2H,s)、7.19-7.24(1H,m)、7.69(1H,s)、7.91(1H,d)、8.65(1H,d)、16.43(1H,s)
1−ベンジル−2−オキソ−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボン酸1.61g(5.7mmol)をジクロロメタン(60mL)に溶解し、塩化オキザリル3.5mL(42mmol)を加えた。この混合物にN,N−ジメチルホルムアミド1滴を加えて40℃で1時間攪拌した。反応溶液を減圧下濃縮し、1−ベンジル−2−オキソ−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボン酸クロリドを得た。得られた酸クロリドをジクロロメタン(60mL)に溶解し、この溶液に1,3−シクロヘキサンジオン0.71g(6.3mmol)とトリエチルアミン0.97mL(6.9mmol)を添加し、室温で2時間攪拌した。反応混合物を炭酸水素ナトリウム水溶液にあけ、ジクロロメタンで抽出し、有機相を乾燥、濃縮した。残渣をジイソプロピルエーテルで洗浄して微黄色固体の標記化合物を2.13g得た(収率 定量的)。
2.10-2.17(2H,m)、2.46(2H,t)、2.72(2H,t)、5.79(2H,s)、6.03(1H,s)、7.22-7.30(4H,m)、7.51-7.54(2H,m)、8.02(1H,d)、8.49(1H,s)、8.75(1H,d)
3−オキソ−1−シクロヘキセニル 1−ベンジル−2−オキソ−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボキシレート2.13g(5.7mmol)をジクロロメタン(60mL)に溶解し、この溶液にトリエチルアミン0.97mL(6.9mmol)とアセトンシアンヒドリン0.54g(6.3mmol)を加え、室温で一昼夜撹拌した。反応混合物をクエン酸水溶液にあけ、ジクロロメタンで抽出し、有機相を水洗、乾燥、濃縮した。残渣をメタノールで洗浄して暗黄色結晶の標記化合物を1.31g得た(収率62%)。
2.06-2.09(2H,m)、2.49(2H,t)、2.74(2H,t)、5.73(2H,s)、7.16-7.27(4H,m)、7.46(1H,d)、7.71(1H,s)、7.90(1H,d)、8.61(1H,d)、16.41(1H,s)
1−(2−メトキシベンジル)−2−オキソ−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボン酸3.83g(12.3mmol)をジクロロメタン(100mL)に溶解し、塩化オキザリル7.5mL(89mmol)を加えた。この混合物にN,N−ジメチルホルムアミド1滴を加えて40℃で1時間攪拌した。反応溶液を減圧下濃縮し、1−(2−メトキシベンジル)−2−オキソ−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボン酸クロリドを得た。得られた酸クロリドをジクロロメタン(100mL)に溶解し、この溶液を1,3−シクロヘキサンジオン1.52g(13.6mmol)とトリエチルアミン2.11mL(14.8mmol)のジクロロメタン(100mL)溶液に氷冷下で添加し、室温で2時間攪拌した、反応混合物を、炭酸水素ナトリウム水溶液にあけ、ジクロロメタンで抽出し、有機相を乾燥、濃縮した。残渣をジイソプロピルエーテルで洗浄して微黄色固体の標記化合物を4.82g得た(収率97%)。
2.06-2.14(2H,m)、2.44(2H,t)、2.71(2H,t)、3.89(3H,s)、5.80(2H,s)、6.03(1H,s)、6.60(1H,d)、6.74(1H,t)、6.88(1H,d)、7.15-7.27(2H,m)、8.05(1H,d)、8.56(1H,s)、8.66(1H,s)
3−オキソ−1−シクロヘキセニル 1−(2−メトキシベンジル)−2−オキソ−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボキシレート4.82g(11.9mmol)をジクロロメタン(100mL)に溶解し、この溶液にトリエチルアミン2.01mL(14.3mmol)とアセトンシアンヒドリン1.11g(13.1mmol)を加え、室温で一昼夜撹拌した。反応混合物をクエン酸水溶液にあけ、ジクロロメタンで抽出し、有機相を水洗、乾燥、濃縮した。残渣をカラムクロマトグラフィー(酢酸エチル:n‐ヘキサン=1:3〜1:1)で精製し黄色結晶の標記化合物を1.59g(収率33%)得た。
2.00-2.08(2H,m)、2.45(2H,t)、2.71(2H,t)、3.90(3H,s)、5.73(2H,s)、6.72-6.80(1H,m)、6.87(1H,d)、7.13-7.18(2H,m)、7.80(1H,s)、7.94(1H,d)、8.54(1H,d)、16.31(1H,s)
2−オキソ−1−フェニル−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボン酸1.62g(6.1mmol)をジクロロメタン(60mL)に溶解し、塩化オキザリル3.7mL(44mmol)を加えた。この混合物にN,N−ジメチルホルムアミド1滴を加えて40℃で1時間攪拌した。反応混合物を減圧下濃縮し、2−オキソ−1−フェニル−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボン酸クロリドを得た。得られた酸クロリドをジクロロメタン(60mL)に溶解し、この溶液に1,3−シクロヘキサンジオン0.75g(6.7mmol)とトリエチルアミン1.03mL(7.3mmol)を添加し、室温で2時間攪拌した。反応混合物を、炭酸水素ナトリウム水溶液にあけ、ジクロロメタンで抽出し、有機相を乾燥、濃縮した。残渣をジイソプロピルエーテルで洗浄して微黄色固体の標記化合物を2.16g(収率99%)得た。
2.06-2.14(2H,m)、2.45(2H,t)、2.70(2H,t)、6.04(3H,s)、7.24-7.29(3H,m)、7.49-7.62(3H,m)、8.08(1H,d)、8.57-8.60(3H,m)
3−オキソ−1−シクロヘキセニル 1−フェニル−2−オキソ−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボキシレート2.16g(6.0mmol)をジクロロメタン(50mL)に溶解し、この溶液にトリエチルアミン1.01mL(7.2mmol)とアセトンシアンヒドリン0.56g(6.6mmol)を加え、室温で一昼夜撹拌した。反応混合物をクエン酸水溶液にあけ、ジクロロメタンで抽出し、有機相を水洗、乾燥、濃縮した。残渣をメタノールで洗浄して淡茶色結晶の標記化合物を1.01g(収率47%)得た。
1.99-2.05(2H,m)、2.44(2H,t)、2.70(2H,t)、7.16-7.19(1H,m)、7.31(2H,d)、7.45-7.49(1H,m)、7.56(2H,t)、7.82(1H,s)、7.95(1H,d)、8.48(1H,d)、16.38(1H,s)
1−(5−メチル−3−イソオキサゾリル)−2−オキソ−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボン酸1.7g(6.3mmol)をジクロロメタン(50mL)に溶解し、塩化オキザリル3.0mL(36mmol)を加えた。この混合物にN,N−ジメチルホルムアミド1滴を加えて室温で1時間攪拌した。反応溶液を減圧下濃縮し、1−(5−メチル−3−イソオキサゾリル)−2−オキソ−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボン酸クロリドを得た。得られた酸クロリドをジクロロメタン(50mL)に溶解し、この溶液に氷冷下で1,3−シクロヘキサンジオン0.77g(6.9mmol)とトリエチルアミン1.1mL(7.5mmol)を添加し、氷冷下で30分攪拌した。この混合物にトリエチルアミン0.97mL(6.9mmol)とアセトンシアンヒドリン0.59g(6.9mmol)を加え、40℃で1時間撹拌した。反応混合物をクエン酸水溶液にあけ、ジクロロメタンで抽出し、有機相を水洗、乾燥、濃縮した。残渣をカラムクロマトグラフィー(酢酸エチル:n‐ヘキサン=1:1〜9:1)で精製し、黄色結晶の標記化合物を0.27g(収率12%)得た。
2.01-2.07(2H,m)、2.46(2H,t)、2.55(1H,s)、2.72(2H,t)、6.21(1H,d)、7.22-7.26(1H,m)、7.81(1H,s)、7.96(1H,d)、8.53(1H,d) 、16.31 (1H,s)
1−(6−メトキシ−3−ピリジニル)−2−オキソ−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボン酸1.35g(4.5mmol)をジクロロメタン(50mL)に溶解し、塩化オキザリル2.5mL(30mmol)を加えた。この混合物にN,N−ジメチルホルムアミド1滴を加えて室温で2時間攪拌した。反応溶液を減圧下濃縮し、1−(6−メトキシ−3−ピリジル)−2−オキソ−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボン酸クロリドを得た。得られた酸クロリドをジクロロメタン(50mL)に溶解し、この溶液に氷冷下で1,3−シクロヘキサンジオン0.56g(5.0mmol)とトリエチルアミン1.54mL(10.8mmol)を添加し、室温で2時間攪拌した。反応混合物を、水にあけ、ジクロロメタンで抽出し、有機相を乾燥、濃縮した。残渣をジイソプロピルエーテルで洗浄して微黄色固体の標記化合物を1.78g(収率 定量的)得た。
2.07-2.16(2H,m)、2.46(2H,t)、2.70(2H,t)、4.01(3H,s)、6.05(1H,s)、6.93(1H,d)、7.29(1H,dd)、7.51(1H,dd)、8.07-8.11(2H,m)、8.58-8.61(2H,m)
3−オキソ−1−シクロヘキセニル 1−(6−メトキシ−3−ピリジル)−2−オキソ−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボキシレート1.78g(4.5mmol)をジクロロメタン(50mL)に溶解し、この溶液にトリエチルアミン0.77mL(5.5mmol)とアセトンシアンヒドリン0.43g(5.0mmol)を加え、室温で一晩撹拌した。反応混合物をクエン酸水溶液にあけ、ジクロロメタンで抽出し、有機相を水洗、乾燥、濃縮した。残渣をカラムクロマトグラフィー(酢酸エチル:n‐ヘキサン=1:1〜7:3)で精製し橙色結晶の標記化合物を0.37g(収率21%)得た。
2.01-2.04(2H,m)、2.44(2H,t)、2.72(2H,t)、3.99(3H,s)、6.91(1H,d)、7.20(1H,dd)、7.54(1H,dd)、7.81(1H,s)、7.97(1H,d)、8.14(1H,d)、8.48(1H,d)、16.36(1H,s)
2.05-2.14(2H,m)、2.45(2H,t)、2.70(2H,t)、4.31(4H,s)、6.04(1H,s)、6.73 (1H,dd)、6.80(1H,d)、7.23-7.28(1H,m)、8.06(1H,dd)、8.57(1H,s)、8.63(1H,dd)
3−オキソ−1−シクロヘキセニル 1−(2,3−ジヒドロベンゾ[b][1,4]ジオキシン−6−イル)−2−オキソ−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボキシレート3.32g(7.9mmol)をアセトニトリル(150mL)に溶解し、この溶液にトリエチルアミン0.88g(8.7mmol)とアセトンシアノヒドリン0.77g(8.7mmol)を加え、室温で一昼夜撹拌した。反応混合物を飽和重曹水にあけ、クロロホルムで洗浄し、水相にクエン酸を加えてpH3〜4としてからクロロホルムで抽出した。有機相を水洗、乾燥、濃縮し、残渣をカラムクロマトグラフィー(酢酸エチル:n‐ヘキサン=1:1〜1:0)で精製し、淡橙色粉末の標記化合物を0.90g(収率27%)得た。
1.98-2.06(2H,m)、2.44(2H,t)、2.70(2H,t)、4.30(4H,s)、6.77(1H,dd)、7.01(1H,d)、7.15-7.19(1H,m)、7.80(1H,s)、7.94(1H,dd)、8.52 (1H,dd)、16.36(1H,s)
1−メチル−2−オキソ−7−(トリフルオロメチル)−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボン酸0.83g(3.0mmol)をジクロロメタン(50mL)に溶解し、塩化オキザリル1.0mL(12mmol)を加えた。この混合物にN,N−ジメチルホルムアミド2滴を加えて40℃で2時間攪拌した。反応溶液を減圧下濃縮し、1−メチル−2−オキソ−7−(トリフルオロメチル)−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボン酸クロリドを得た。得られた酸クロリドをアセトニトリル(30mL)に溶解し、この溶液を1,3−シクロヘキサンジオン0.38g(3.4mmol)とトリエチルアミン0.51mL(3.7mmol)のアセトニトリル(50mL)溶液に氷冷下で添加し、室温で2時間攪拌した。反応混合物を水にあけ、酢酸エチルで抽出し、有機相を水、炭酸水素ナトリウム水溶液、水の順で洗浄し、乾燥、濃縮した。残渣をジイソプロピルエーテルで洗浄して褐色結晶の標記化合物を0.51g(収率46%)得た。
2.05-2.17(2H,m)、2.49(2H,t)、2.73(2H,t)、3.89(3H,s)、6.05(1H,s)、7.61(1H,d, J=8.1Hz)、8.22(1H,d, J=8.0Hz)、8.49(1H,s)
3−オキソ−1−シクロヘキセニル 1−メチル−2−オキソ−7−(トリフルオロメチル)−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボキシレート0.51g(1.4mmol)をアセトニトリル(50mL)に溶解し、この溶液にトリエチルアミン0.15g(1.5mmol)とアセトンシアノヒドリン0.14g(1.6mmol)を加え、室温で一昼夜撹拌した。反応混合物を飽和重曹水にあけ、酢酸エチルで洗浄し、水相にクエン酸を加えてpH3〜4としてから酢酸エチルで抽出した。有機相を水洗、乾燥、濃縮し、残渣をジイソプロピルエーテルで洗浄して微褐色結晶の標記化合物を0.17g(収率33%)得た。
2.03-2.12(2H,m)、2.47H,t)、2.77(2H,t)、3.83(3H,s)、7.53(1H,d, J=8.0Hz)、7.73(1H,s)、8.06 (1H,d, J=7.7Hz)、16.5(1H,s)
(製造中間体)1−メチル−2−オキソ−1,2−ジヒドロキノリン−3−カルボン酸の製造(製造中間体の化合物番号VIII−1)
2−ニトロベンズアルデヒド32.3g(0.21mol)とマロン酸ジエチル35.0g(0.21mol)とを室温下で無水酢酸100mLに加え、この混合物に炭酸水素ナトリウム27.0g(0.32mol)を加えて100℃で一晩反応させた。反応混合物をおよそ半分まで減圧濃縮し、この反応混合物に氷水を加えて酢酸エチルで抽出した。有機相を、炭酸水素ナトリウム水溶液、水の順に洗浄し、乾燥、減圧濃縮した。残渣をカラムクロマトグラフィー(酢酸エチル:n‐ヘキサン=1:9〜1:4)で精製し、微黄色結晶の標記化合物を37.0g(収率59%)得た。
1.02(3H,t)、1.38(3H,t)、4.08(2H,q)、4.35(2H,q)、7.43(1H,d)、7.55-7.67(2H,m)、8.20(1H,s)、8.22(1H,d)
ジエチル 2−(2−ニトロベンジリデン)マロネート29.0g(0.21mol)を室温下で酢酸100mLに加え、80℃に加温した。この混合物に、鉄粉37.0g(0.66mol)を徐々に加え、反応温度が100℃まで上昇した。反応温度が下降した後、80℃で5時間反応させた。室温冷却後、酢酸エチルと水を加え、不溶物をろ過し、ろ液に炭酸水素ナトリウムを加えて中和した。析出した固体をろ別し、この固体を酢酸エチルに溶解させた。さらにろ液を酢酸エチルで抽出し、前記の溶液とあわせ、この溶液をクエン酸、水の順で洗浄し、乾燥、濃縮した。残渣をジイソプロピルエーテルで洗浄して、淡黄色結晶の標記化合物を13.6g(収率63%)得た。
1.46(3H,t)、4.46(2H,q)、7.26(1H,t)、7.51(1H,d)、7.59-7.67(2H,m)、8.57(1H,s)、12.59(1H,s)
エチル 2−オキソ−1,2−ジヒドロキノリン−3−カルボキシレート3.5g(16mmol)をN,N−ジメチルホルムアミド(80mL)と1,2−ジメトキシエタン(25mL)の混合溶媒に溶解し、窒素気流下、室温下で60%水素化ナトリウム(油性)0.71g(18mmol)を加え、室温で15分撹拌した。この混合物に、室温下で臭化リチウム5.6g(64mmol)を加え、室温で15分撹拌し、さらにヨードメタン4.6g(32mmol)を室温下で加え60℃で3時間撹拌した。反応混合物をクエン酸水溶液に注ぎ、酢酸エチルで抽出し、有機相を食塩水、炭酸水素ナトリウム水溶液、食塩水の順で洗浄し、乾燥、濃縮した。残渣をカラムクロマトグラフィー(酢酸エチル:n‐ヘキサン=1:4〜4:1)で精製し、微黄色結晶の標記化合物を2.4g(収率64%)得た。
1.42(3H,t)、3.75(3H,s)、4.43(2H,q)、7.27 (1H,t)、7.37(1H,d)、7.64-7.69(2H,m)、8.39(1H,s)
エチル 1−メチル−2−オキソ−1,2−ジヒドロキノリン−3−カルボキシレート2.4g(10.4mmol)を1,4−ジオキサン(50mL)に溶解し、この溶液に室温で水酸化リチウム一水和物0.65g(15mmol)と水10mLを加え、室温で24時間撹拌した。反応混合物を炭酸水素ナトリウム水溶液にあけ、酢酸エチルで洗浄し、水相をクエン酸で酸性にしてからクロロホルムで抽出した。有機相を水洗、乾燥、濃縮し、得られた残渣を酢酸エチルで洗浄して微黄色結晶の標記化合物を2.02g(収率96%)得た。
3.88(3H,s)、7.45(1H,t)、7.53(1H,d)、7.82(1H,t)、8.93(1H,s)、14.55(1H,s)
(製造中間体)1−メチル−2−オキソ−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボン酸の製造(製造中間体の化合物番号VIII−4)
(1)3−ホルミル−2−(ピバロイルアミノ)ピリジンの製造
2−(ピバロイルアミノ)ピリジン11.4g(64mmol)をテトラヒドロフラン50mLに溶解し、1.6Mノルマルブチルリチウム100mL(0.16mol)を−60℃で滴下し、さらに−10℃で3時間反応させた。この反応混合物に、−60℃で、N,N−ジメチルホルムアミド14g(0.19mol)を滴下し、反応液を室温で一晩撹拌した。反応混合物を氷にあけ、6N−塩酸を加えて酸性にした後、炭酸カリウムを加えてアルカリ性にし酢酸エチルで抽出した。有機相を水で洗浄し、乾燥、濃縮し、得られた残渣をカラムクロマトグラフィー(酢酸エチル:n‐ヘキサン=1:4〜1:0)で精製し淡黄色液体の標記化合物を6.57g(収率50%)得た。
1.38(9H,s)、7.19-7.22(1H,m)、8.05(1H,dd)、8.69(1H,dd)、9.94(1H,s)、10.90(1H,br)
3−ホルミル−2−(ピバロイルアミノ)ピリジン6.57g(32mmol)をエタノール(50mL)に溶解し、この溶液にマロン酸ジエチル10.2g(64mmol)とピロリジン1.6mL(16mmol)を加え100℃で一晩撹拌した。反応混合物を室温冷却し、析出した固体をエタノールで洗浄して黄色固体の標記化合物を2.2g(収率32%)得た。
1H−NMRデータ(CDCl3/TMS δ(ppm)):
1.44(3H,t)、4.45(2H,q)、7.26-7.30(1H,m)、8.05(1H,dd)、8.47(1H,s)、9.93(1H,dd)
エチル 2−オキソ−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボキシレート2.2g(10mmol)をN,N−ジメチルホルムアミド(50mL)と1,2−ジメトキシエタン(15mL)の混合溶媒に溶解し、窒素気流下、室温下で60%水素化ナトリウム(油性)0.45g(11mmol)を加え、さらに室温で30分撹拌した。この混合物に、氷冷下、臭化リチウム3.5g(40mmol)をを加え、室温で30分撹拌し、さらにヨードメタン3.9g(27.5mmol)を室温下で加え、60℃で6時間撹拌した。反応混合物をクエン酸水溶液に注ぎ、酢酸エチルで抽出し、有機相を食塩水、炭酸水素ナトリウム水溶液、食塩水の順で洗浄し、乾燥、濃縮した。残渣をジイソプロピルエーテルで洗浄して微紫色固体の標記化合物を1.66g(収率71%)得た。
1.42(3H,t)、3.87(3H,s)、4.43(2H,q)、7.21-7.25(1H,m)、7.97(1H,dd)、8.34(1H,s)、8.69(1H,dd)
エチル 1−メチル−2−オキソ−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボキシレート1.66g(7.1mmol)を1,4−ジオキサン(50mL)に溶解し、室温で水酸化リチウム一水和物0.45g(11mmol)と水10mLを加え、室温で1.5時間撹拌した。反応混合物を炭酸水素ナトリウム水溶液にあけ、酢酸エチルで洗浄した。水相をクエン酸で酸性にしてから酢酸エチルで抽出し、有機相を水洗、乾燥、濃縮した。残渣をジイソプロピルエーテルで洗浄して無色結晶の標記化合物を1.30g(収率89%)得た。
3.99(3H,s)、7.39-7.43(1H,m)、8.16(1H,dd)、7.83(1H,dd)、8.92(1H,s)、14.34(1H,s)
(製造中間体)1−(エチルチオメチル)−2−オキソ−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボン酸の製造(製造中間体の化合物番号VIII−8)
(1)(2−(メチルアミノ)−3−ピリジニル)メタノールの製造
2−クロロニコチン酸30.0g(0.19mol)をN,N−ジメチルホルムアミド(400mL)に溶解し、メチルアミン塩酸塩31.0g(0.38mol)と炭酸カリウム105g(0.76mol)、臭化銅(I)2.73g(19.0mmol)を加え100℃で20時間撹拌した。室温に冷却後、不溶物をろ過し、ろ液を濃縮した。得られた残渣に10%水酸化ナトリウム水溶液を加え、ジエチルエーテルで洗浄した。水相に濃塩酸を加えてpH6〜7とし、水相を濃縮して得られた個体を乾燥して粗製の2−(メチルアミノ)ニコチン酸を得た。
2.10(1H,s)、3.01(3H,d)、4.59(2H,s)、5.38(1H,s)、6.48-6.52(1H,m)、7.21(1H,d)、8.01(1H,d)
(2−(メチルアミノ)−3−ピリジニル)メタノール9.10g(66.0mmol)をクロロホルム(70mL)に溶解し、二酸化マンガン17.4g(200mmol)を加えて60℃で一晩撹拌した。反応混合物をろ過し、ろ液を濃縮して橙色固体の標記化合物を8.66g(収率96%)得た。
3.10(3H,d)、6.62-6.66(1H,m)、7.74(1H,d)、8.36(1H,d)、9.80(1H,s)
2−(メチルアミノ)ニコチンアルデヒド8.66g(64.5mmol)をメタノール(100mL)に溶解し、マロン酸ジメチル12.68g(96.0mmol)とピペリジン2.18g(25.6mmol)を加え80℃で7時間撹拌した。冷却して析出した固体をろ別し、ジイソプロピルエーテルで洗浄して淡黄色固体の標記化合物を11.71g(収率84%)得た。
3.87(3H,s)、3.97(3H,s)、7.21-7.27(1H,m)、7.98(1H,d)、8.39(1H,s)、8.70(1H,d)
メチル 1−メチル−2−オキソ−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボキシレート10.71g(49.0mmol)を四塩化炭素(200mL)に溶解し、N−ブロモこはく酸イミド8.64g(49.0mmol)と1,2−アゾビス(2−メチルプロピオニトリル)0.1gを加えて、光を照射しながら4時間撹拌した。さらに、N−ブロモこはく酸イミド3.0g(17.0mmol)を加え、光を照射しながら3時間撹拌した。反応混合物を水にあけ、クロロホルムで抽出し、有機相を水洗、乾燥、濃縮した。残渣をカラムクロマトグラフィー(酢酸エチル:クロロホルム=1:19)で精製し無色結晶の標記化合物を10.56g(収率73%)得た。
3.98(3H,s)、6.36(2H,d, J=85.3Hz)、7.32-7.35(1H,m)、8.02(1H,d)、8.46(1H,s)、8.78(1H,d)
メチル 1−(ブロモメチル)−2−オキソ−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボキシレート3.00g(10.1mmol)をN,N−ジメチルホルムアミド(40mL)に溶解し、エタンチオール0.94g(15.1mmol)と炭酸カリウム2.09g(15.1mmol)を加えて、室温で一晩撹拌した。反応混合物を水にあけ、酢酸エチルで抽出し、有機相を水洗、乾燥、濃縮して、淡黄色結晶の標記化合物を2.85g(収率 定量的)得た。
1.31(3H,t)、2.84(2H,q)、3.97(3H,s)、5.68(2H,s)、7.23-7.28(1H,m)、7.99(1H,d)、8.41(1H,s)、8.71(1H,d)
メチル 1−(エチルチオメチル)−2−オキソ−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボキシレート2.81g(10.1mmol)を1,4−ジオキサン(70mL)に溶解し、室温で6N塩酸(20mL)を加え、50℃で3時間撹拌した。反応混合物の溶媒を減圧留去し、得られた残渣を水、ジイソプロピルエーテルで順次洗浄し、淡黄色結晶の標記化合物を2.20g得た(収率82%)。
1.33(3H,t)、2.71(2H,q)、5.77(2H,s)、7.41-7.45(1H,m)、8.18(1H,d)、8.84(1H,d)、8.92(1H,s)、14.06(1H,s)
(製造中間体)1−ベンジル−2−オキソ−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボン酸の製造(製造中間体の化合物番号VIII−9)
(1)エチル 1−ベンジル−2−オキソ−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボキシレートの製造
エチル 2−オキソ−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボキシレート1.50g(6.9mmol)をN,N−ジメチルホルムアミド(30mL)に溶解し、炭酸カリウム1.43g(10.4mmol)と臭化ベンジル1.36g(7.9mmol)を加え、室温で一昼夜撹拌した。反応混合物を水に注ぎ、ジエチルエーテルで抽出し、有機相を乾燥、ろ過、濃縮した。残渣をカラムクロマトグラフィー(酢酸エチル:n‐ヘキサン=3:7〜1:1)で精製し、無色結晶の標記化合物を1.95g(収率92%)得た。
1.41(3H,t)、4.42(2H,q)、5.78(2H,s)、7.18-7.28(4H,m)、7.52(2H,d)、7.96(1H,d)、6.35(1H,s)、8.69(1H,s)
エチル 1−ベンジル−2−オキソ−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボキシレート1.95g(6.3mmol)を1,4−ジオキサン(30mL)に溶解し、この溶液に室温で炭酸カリウム1.31g(9.5mmol)と水60mLを加え、50℃で3時間撹拌した。反応混合物の溶媒を減圧留去し、残渣を水に溶解し、濃塩酸を加え酸性とし、クロロホルムで抽出した。有機相を乾燥、ろ過、濃縮し、無色結晶の標記化合物を1.71g(収率97%)得た。
5.88(2H,s)、7.26-7.33(3H,m)、7.39-7.43(1H,m)、7.51(2H,d)、8.16(1H,d)、8.85(1H,d)、8.91(1H,s)、14.27(1H,s)
(製造中間体)1−(2−メトキシベンジル)−2−オキソ−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボン酸の製造(製造中間体の化合物番号VIII−20)
(1)2−(2−メトキシベンジルアミノ)ニコチン酸の製造
2−クロロニコチン酸7.00g(44.2mmol)と2−メトキシベンジルアミン12.13g(88.4mmol)を140℃で4時間加熱した。室温に放冷後、反応混合物に10%水酸化ナトリウム水溶液を加え、クロロホルムで洗浄した。水相に濃塩酸を加えてpH6〜7とし、析出した個体をろ別、乾燥し、淡黄色粉末の標記化合物を8.50g(収率74%)得た。
3.87(3H,s)、4.78(2H,s)、6.52-6.56(1H,m)、6.87-6.92(2H,m)、7.23-7.33(2H,m)、8.18(1H,d)、8.33(1H,d)、8.34(1H,s)
窒素気流下、氷冷下で水素化リチウムアルミニウム2.50g(65.8mmol)をテトラヒドロフラン(100mL)に加え、この溶液に2−(2−メトキシベンジルアミノ)ニコチン酸8.50g(32.9mmol)のテトラヒドロフラン(70mL)溶液を滴下し、室温下で1時間撹拌した。反応混合物に酢酸エチルを加え、次に10%水酸化ナトリウム水溶液26.4mLを加え、不溶物をろ過した。ろ液を濃縮し、得られた残渣を酢酸エチルに溶解し、乾燥、ろ過、濃縮して、淡黄色粘稠体の標記化合物を8.18g(収率 定量的)得た。
7.96(1H,br)、3.85(3H,s)、4.56(2H,s)、4.68(2H,d)、5.80(1H,s)、6.47-6.51(1H,m)、6.86-6.92(2H,m)、7.20-7.26(2H,m)、7.33(1H,d)、8.08(1H,d)
(2−(2−メトキシベンジルアミノ)−3−ピリジニル)メタノール8.03g(32.9mmol)をクロロホルム(100mL)に溶解し、二酸化マンガン8.60g(98.7mmol)を加えて60℃で一晩撹拌した。反応混合物をろ過し、ろ液を濃縮して橙色個体の標記化合物を7.40g(収率93%)得た。
3.90(3H,s)、4.80(2H,d)、6.59-6.64(1H,m)、6.88-6.92(2H,m)、7.22-7.33(2H,m)、7.72(1H,d)、8.33(1H,d)、8.83(1H,s)、9.80(1H,s)
2−(2−メトキシベンジルアミノ)ニコチンアルデヒド7.40g(30.5mmol)をエタノール(100mL)に溶解し、マロン酸ジエチル7.34g(45.8mmol)とピペリジン0.95g(10.0mmol)を加え100℃で48時間撹拌した。冷却して析出した固体を濾別し、ヘキサンで洗浄して淡黄色固体の標記化合物を7.71g(収率75%)得た。
1.41(3H,t)、3.90(3H,s)、4.42(2H,q)、5.79(2H,s)、6.59(1H,d)、6.73(1H,t)、6.88(1H,d)、7.14-7.22(2H,m)、8.00(1H,d)、8.61(1H,d)
エチル 1−(2−メトキシベンジル)−2−オキソ−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボキシレート3.00g(8.90mmol)を1,4−ジオキサン(90mL)に溶解し、室温で6N塩酸(16mL)を加えた。50℃で5時間撹拌した後、反応混合物から溶媒を減圧留去した。残渣を水で洗浄、乾燥して無色結晶の標記化合物を2.80g(収率 定量的)得た。
3.91(3H,s)、5.90(2H,s)、6.57(1H,d)、6.78(1H,t)、6.93(1H,d)、7.21-7.30(1H,m)、7.37-7.41(1H,m)、8.19(1H,d)、8.77(1H,d)、8.98(1H,s)、14.24(1H,s)
(製造中間体)2−オキソ−1−フェニル−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボン酸の製造(製造中間体の化合物番号VIII−16)
(1)2−(フェニルアミノ)ニコチン酸の製造
2−クロロニコチン酸5.0g(31.7mmol)とアニリン5.9g(63.5mmol)、ヨウ化カリウム0.1gを140℃まで加熱し、この反応混合物にトルエン(30ml)を加え100℃で2時間撹拌した。反応混合物を冷却後、溶媒を留去し、残渣にクロロホルムを加え不溶物をろ過した。ろ液を濃縮して粗製の淡黄色結晶の標記化合物を7.5g得た(収率 定量的)。
6.76-6.79(1H,m)、7.09(1H,t)、7.35(2H,t)、7.59(2H,d)、8.33-8.39(2H,m)、10.27(1H,s)、10.59(1H,s)
窒素気流下、氷冷下で水素化リチウムアルミニウム2.41g(63.4mmol)をテトラヒドロフラン(80mL)に加え、この溶液に2−(フェニルアミノ)ニコチン酸6.79g(31.7mmol)のテトラヒドロフラン(30mL)溶液を滴下し、室温下で2時間撹拌した。反応混合物に、酢酸エチルを加え、さらに10%水酸化ナトリウム水溶液25mLを加え、不溶物をろ過した。ろ液を濃縮し、得られた残渣を酢酸エチルに溶解し、乾燥、ろ過、濃縮して黄色粘稠体の標記化合物を6.9g得た(収率 定量的)。
1.89(1H,s)、4.70(2H,s)、6.69-6.73(1H,m)、6.99(1H,t)、7.29-7.37(3H,m)、7.56(2H,d)、7.68(1H,s)、8.19(1H,d)
(2−フェニルアミノ−3−ピリジニル)メタノール6.35g(31.7mmol)をクロロホルム(100mL)に溶解し、二酸化マンガン8.27g(95.1mmol)を加えて60℃で7時間撹拌した。反応混合物をろ過し、ろ液を濃縮して橙色個体の標記化合物を6.58g得た(収率 定量的)
1H−NMRデータ(CDCl3/TMS δ(ppm)):
6.82-6.86(1H,m)、7.10(1H,t)、7.34-7.39(2H,m)、7.74(2H,d)、7.86(1H,d)、8.42(1H,d)、9.88(1H,s) 、10.45(1H,s)
2−(フェニルアミノ)ニコチンアルデヒド6.28g(31.7mmol)をエタノール(150mL)に溶解し、マロン酸ジエチル7.62g(47.6mmol)とピペリジン1.35g(15.9mmol)を加え100℃で一晩撹拌した。反応混合物を冷却して析出した固体を濾別し、エタノール、ジイソプロピルエーテルで順次洗浄して淡黄色固体の標記化合物を7.42g得た(収率80%)。
1.40(3H,t)、4.42(2H,q)、7.19-7.22(1H,m)、7.26-7.28(2H,m)、7.47-7.51(1H,m)、7.54-7.59(2H,m)、8.02(1H,d)、8.44(1H,s) 、8.53(1H,d)
エチル 2−オキソ−1−フェニル−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボキシレート2.00g(6.8mmol)を1,4−ジオキサン(100mL)に溶解し、室温で炭酸カリウム1.41g(10.2mmol)と水200mLを加え、50℃で3時間撹拌した。反応混合物から溶媒を減圧留去し、残渣を水に溶解し、そこへ濃塩酸を加え酸性とした。析出した個体をろ別、乾燥して淡黄色結晶の標記化合物を1.72g得た(収率95%)。
7.30-7.32(2H,m)、7.38-7.41(1H,m)、7.57-7.67(3H,m)、8.23(1H,d)、8.67(1H,d)、9.05(1H,s)、13.91(1H,s)
(製造中間体)1−(5−メチル−3−イソオキサゾリル)−2−オキソ−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボン酸の製造(製造中間体の化合物番号VIII−24)
(1)メチル 2−(トリフルオロメチルスルホニルオキシ)ニコチネートの製造
メチル 2−ヒドロキシニコチネート10.3g(70mmol)をジクロロメタン300mLに溶解し、トリエチルアミン7.8g(77mmol)を加え、この混合物に、無水トリフルオロメタンスルホン酸20.9g(74mmol)を−60℃で滴下し、さらに−60℃で30分反応させた。反応混合物を水にあけジクロロメタンで抽出し、有機相を水で洗浄後、乾燥、濃縮した。残渣をカラムクロマトグラフィー(酢酸エチル:n‐ヘキサン=1:4)で精製し淡黄色液体の標記化合物を12.8g得た(収率67%)。
4.00(3H,s)、7.49-7.53(1H,m)、8.49(1H,dd)、8.54(1H,dd)
メチル 2−(トリフルオロメチルスルホニルオキシ)ニコチネート6.7g(24mmol)と3−アミノ−5−メチルイソオキサゾール3.0g(31mmol)をトルエン(100mL)に溶解し、炭酸セシウム13.1g(40mmol)、トリス(ジベンジリデンアセトン)ジパラジウム(0)1.5g(1.6mmol)、4,5−ビス(ジフェニルホスフィノ)−9,9−ジメチルキサンテン1.9g(3.4mmol)を加え80℃で1時間加熱撹拌した。反応混合物を冷却後、溶媒を留去し残渣をカラムクロマトグラフィー(酢酸エチル:n‐ヘキサン=1:4)で精製し、橙色粘稠体の標記化合物を4.3g得た(収率78%)。
2.42(3H,s)、3.94(3H,s)、6.81-6.86(2H,m)、8.26(1H,d)、8.41(1H,d)、10.46(1H,dd)
窒素気流下、氷冷下で水素化リチウムアルミニウム0.75g(20mmol)をテトラヒドロフラン(70mL)に加え、この溶液にメチル 2−(5−メチル−3−イソオキサゾリル)アミノニコチネート2.3g(9.9mmol)のテトラヒドロフラン(30mL)溶液を滴下し、氷冷下で1時間撹拌した。反応混合物に、酢酸エチルを加えて、さらに10%水酸化ナトリウム水溶液8.0mLを加え、不溶物をろ過した。ろ液を濃縮し、残渣を酢酸エチルに溶解し、乾燥、ろ過、濃縮して濃縮して橙色粘稠体標記化合物を2.2g得た(収率 定量的)。
2.37(1H,br)、2.41(3H,s)、4.74(2H,s)、6.77-6.82(2H,m)、7.41(1H,d)、8.21(1H,d)、8.27(1H,s)
(2−(5−メチル−3−イソオキサゾリル)アミノ−3−ピリジニル)メタノール3.3g(16mmol)をクロロホルム(60mL)に溶解し、二酸化マンガン4.3g(49mmol)を加えて60℃で48時間撹拌した。反応混合物をろ過し、ろ液を濃縮して橙色粘稠体の標記化合物を3.3g得た(収率 定量的)。
2.43(3H,s)、6.90(1H,s)、6.95-7.00(1H,m)、7.94(1H,d)、8.46(1H,d)、9.92(1H,s)、10.68(1H,s)
(2−(5−メチル−3−イソオキサゾリル)アミノ)ニコチンアルデヒド3.3g(16mmol)をエタノール(60mL)に溶解し、マロン酸ジエチル3.9g(24mmol)とピペリジン0.56g(6.5mmol)を加え90℃で一晩撹拌した。反応混合物を冷却後、溶媒を留去し、残渣をカラムクロマトグラフィー(酢酸エチル:n‐ヘキサン=1:4〜7:3)で精製し、淡黄色結晶の標記化合物を2.7g得た(収率55%)。
1.40(3H,t)、2.57(3H,s)、4.42(2H,q)、6.19(1H,s)、7.25-7.29(1H,m)、8.03(1H,d)、8.50(1H,s)、8.58(1H,d)
エチル 1−(5−メチル−3−イソオキサゾリル)−2−オキソ−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボキシレート1.8g(6.0mmol)を酢酸(50mL)に溶解し、この溶液に室温で6N塩酸(10mL)を加え、さらに60℃で5時間撹拌した。反応混合物から、溶媒を留去し、残渣をトルエンに溶解し、溶媒を減圧留去して無色結晶の標記化合物を1.7g得た(収率 定量的)。
2.62(3H,s)、6.24(1H,s)、7.43-7.47(1H,d)、8.23(1H,d)、8.71(1H,d)、9.04(1H,s)、13.32(1H,br)
(製造中間体)1−(6−メトキシ−3−ピリジニル)−2−オキソ−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボン酸の製造(製造中間体の化合物番号VIII−25)
(1)メチル 2−クロロニコチネートの製造
2−クロロニコチン酸15.0g(95.2mmol)をジクロロメタン(150mL)に溶解し、塩化オキザリル8.37mL(94.5mmol)を加えた、この混合物にN,N−ジメチルホルムアミド6滴を加えて室温で3時間攪拌した。この反応混合物に氷冷下、トリエチルアミン40.1mL(286mmol)とメタノール37mL(914mmol)を順次滴下して、氷冷下で30分撹拌した。反応混合物から溶媒を減圧留去後、残渣に炭酸水素ナトリウム水溶液を加え、ジエチルエーテルで抽出した。有機相を水洗、乾燥、濃縮し、残渣をカラムクロマトグラフィー(酢酸エチル:n‐ヘキサン=1:4)で精製し、淡黄色液体の標記化合物を13.9g得た(収率86%)。
3.97(3H,s)、7.33(1H,dd)、8.17(1H,dd)、8.53(1H,dd)
メチル 2−クロロニコチネート5.0g(29mmol)と6−メトキシピリジン−3−アミン4.3g(35mmol)をトルエン(80mL)に溶解し、炭酸セシウム16.1g(50mmol)、トリス(ジベンジリデンアセトン)ジパラジウム(0)1.3g(1.5mmol)、4,5−ビス(ジフェニルホスフィノ)−9,9−ジメチルキサンテン1.8g(3.1mmol)を加え90℃で72時間加熱撹拌した。反応混合物から、溶媒を留去し、水と酢酸エチルを加えてろ過した。ろ液を酢酸エチルで抽出し、有機相を乾燥、濃縮し、残渣をカラムクロマトグラフィー(酢酸エチル:n‐ヘキサン=1:4〜1:1)で精製し淡黄色粘稠体の標記化合物を6.8g得た(収率96%)。
3.94(6H,s)、6.68-6.77(2H,m)、7.94(1H,dd)、8.22(1H,dd)、8.31(1H,dd)、8.36(1H,d)、9.88(1H,s)
窒素気流下、氷冷下で水素化リチウムアルミニウム2.1g(56mmol)をテトラヒドロフラン(100mL)に加え、この溶液にメチル 2−(6−メトキシ−3−ピリジニル)アミノニコチネート6.8g(28mmol)のテトラヒドロフラン(60mL)溶液を滴下し、室温下で2時間撹拌した。反応混合物に、酢酸エチルを加えて、さらに10%水酸化ナトリウム水溶液23mLを加え、不溶物をろ過した。ろ液を濃縮し、残渣を酢酸エチルに溶解し、乾燥、ろ過、濃縮して黄色粘稠体の標記化合物を6.6g得た(収率 定量的)。
1.67(1H,br)、3.92(3H,s)、4.72(2H,s)、6.66-6.75(2H,m)、7.33(1H,dd)、7.51(1H,s)、7.91(1H,dd)、8.10(1H,dd)、8.21(1H,d)
(2−(6−メトキシ−3−ピリジニル)アミノ−3−ピリジニル)メタノール6.48g(28mmol)をクロロホルム(200mL)に溶解し、二酸化マンガン7.3g(84mmol)を加えて50℃で48時間撹拌した。反応混合物をろ過し、ろ液を濃縮して橙色個体の標記化合物を6.5g得た(収率 定量的)。
3.94(3H,s)、6.76(1H,d)、6.84(1H,dd)、7.88(1H,dd)、7.96(1H,dd)、8.37(1H,dd)、8.42(1H,d)、9.90(1H,d)、10.20(1H,s)
2−(6−メトキシ−3−ピリジニルアミノ)ニコチンアルデヒド6.4g(28mmol)をエタノール(50mL)に溶解し、マロン酸ジエチル6.7g(42mmol)とピペリジン0.95g(11mmol)を加え100℃で4時間撹拌した。反応混合物から溶媒を減圧留去し、残渣を酢酸エチルとジイソプロピルエーテルの混合溶液で洗浄して、淡黄色固体の標記化合物を4.1g得た(収率45%)。
1.41(3H,t)、4.00(3H,s)、4.43(2H,q)、6.92(1H,d)、7.24(1H,dd)、7.51(1H,dd)、8.03(1H,d)、8.08(1H,d)、8.49(1H,s)、8.54(1H,dd)
エチル (6−メトキシ−3−ピリジニル)−2−オキソ−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボキシレート4.1g(13mmol)を1,4−ジオキサン(60mL)に溶解し、室温で炭酸カリウム2.6g(19mmol)と水100mLを加え、60℃で3時間撹拌した。反応混合物から溶媒を減圧留去し、残渣を水に溶解し、クロロホルムで洗浄した。水相に濃塩酸を加え酸性とし、クロロホルムで抽出し、有機相を乾燥、濃縮して無色結晶の標記化合物を1.45g得た(収率39%)。
4.04(3H,s)、6.99(1H,d)、7.42(1H,dd)、7.52(1H,dd)、8.12(1H,d)、8.23(1H,d)、8.68(1H,dd)、9.04(1H,s)、13.76(1H,s)
(製造中間体)1−(2,3-ジヒドロベンゾ[b][1,4]ジオキシン−6−イル)−2−オキソ−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボン酸の製造(製造中間体の化合物番号VIII−26)
(1)メチル 2−(トリフルオロメチルスルホニルオキシ)ニコチネートの製造
メチル 2−ヒドロキシニコチネート12.4g(81mmol)をジクロロメタン150mLに溶解し、トリエチルアミン9.0g(89mmol)を加えた後、無水トリフルオロメタンスルホン酸25.1g(89mmol)を−30℃で滴下した。反応混合物を室温下で5時間反応させ、水にあけ室温で1時間攪拌した後、ジクロロメタンで抽出た。有機相を水で洗浄後、乾燥、濃縮して橙色液体の標記化合物21.2gを得た(収率92%)。
4.00(3H,s)、7.49-7.53(1H,m)、8.49(1H,dd)、8.54(1H,dd)
メチル 2−(トリフルオロメチルスルホニルオキシ)ニコチネート10.6g(37mmol)と3,4−エチレンジオキシベンジルアミン6.2g(41mmol)をトルエン(100mL)に溶解し、炭酸セシウム17.0g(52mmol)、トリス(ジベンジリデンアセトン)ジパラジウム(0)1.0g(1.1mmol)、4,5−ビス(ジフェニルホスフィノ)−9,9−ジメチルキサンテン1.3g(5.2mmol)を加え80℃で2時間加熱撹拌した。反応混合物から溶媒を留去し、水と酢酸エチルを加えてろ過した。ろ液を酢酸エチルで抽出し、有機相をクエン酸水溶液、水の順で洗浄後、乾燥、濃縮した。残渣をカラムクロマトグラフィー(酢酸エチル:n‐ヘキサン=1:9〜1:2)で精製し橙色粘稠体の標記化合物を9.86g得た(収率93%)。
1H−NMRデータ(CDCl3/TMS δ(ppm)):
3.91(3H,s)、4.24(4H,br)、6.64-6.66(1H,m)、6.83(1H,d)、6.97(1H,dd)、7.37(1H,d)、8.19(1H,dd)、8.33(1H,dd)、9.92(1H,br)
窒素気流下、氷冷下で水素化リチウムアルミニウム1.70g(41mmol)をテトラヒドロフラン(100mL)に加え、メチル 2−(2,3−ジヒドロベンゾ[b][1,4]ジオキシン−6−イル)アミノニコチネート9.86g(34mmol)のテトラヒドロフラン(30mL)溶液を滴下した。反応混合物に、酢酸エチルを加え、続いて10%水酸化ナトリウム水溶液17mLを加え、不溶物をろ過した。ろ液を濃縮し、残渣を酢酸エチルに溶解し、乾燥、ろ過、濃縮して橙色粘稠体の標記化合物を8.9g得た(収率 定量的)た。
2.78(1H,br)、4.20(4H,br)、4.56(1H,s)、6.59-6.63(1H,m)、6.77-6.86(2H,m)、7.18-7.26(2H,m)、7.47(1H,br)、8.07(1H,dd)
2−(2,3−ジヒドロベンゾ[b][1,4]ジオキシン−6−イル)アミノ−3−ピリジニルメタノール8.9g(34mmol)をクロロホルム(100mL)に溶解し、二酸化マンガン10.1g(0.10mol)を加えて50℃で一晩撹拌した。反応混合物をろ過し、濃縮して得られた残渣を酢酸エチルに溶解し、乾燥、ろ過、濃縮して得られた油状物をカラムクロマトグラフィー(酢酸エチル:n‐ヘキサン=1:9〜1:1)で精製し橙色粘稠体の標記化合物を7.69g得た(収率87%)。
4.26(4H,br)、6.77-6.81(1H,m)、6.87(1H,d)、7.43(1H,d)、7.82(1H,dd)、8.38(1H,dd)、9.85(1H,s) 、10.25(1H,br)
(2−(2,3−ジヒドロベンゾ[b][1,4]ジオキシン−6−イル)アミノ)ニコチンアルデヒド7.69g(30mmol)をエタノール(150mL)に溶解し、マロン酸ジエチル7.2g(45mmol)とピロリジン1.5mL(15mmol)を加え100℃で一晩撹拌した。冷却して析出した固体をカラムクロマトグラフィー(酢酸エチル:n‐ヘキサン=1:1〜1:0)で精製し淡黄色固体の標記化合物を4.3g得た(収率41%)。
1.40(3H,t)、4.31(4H,br)、4.42(2H,q)、6.73(1H,dd)、6.79(1H,d)、7.03(1H,d)、7.18-7.23(1H,m)、8.00(1H,dd)、8.46(1H,s)、8.58(1H,dd)
エチル 1−(2,3−ジヒドロベンゾ[b][1,4]ジオキシン−6−イル)−2−オキソ−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボキシレート4.3g(12mmol)を1,4−ジオキサン(100mL)に溶解し、室温で水酸化リチウム一水和物1.0g(24mmol)と水50mLを加え、室温で一晩撹拌した。反応混合物に水を加え、析出した固体をクロロホルムに溶解した。この溶液をクエン酸水溶液、水の順で洗浄し、乾燥、濃縮し、得られた固体をジイソプロピルエーテルで洗浄して淡黄色結晶の標記化合物を3.96g得た(収率 定量的)。
4.34(4H,br)、6.75(1H,dd)、6.82(1H,d)、7.09(1H,d)、7.37-7.42(1H,m)、8.20(1H,dd)、8.72(1H,dd)、9.02(1H,s) 、13.94(1H,s)
(製造中間体)1−メチル−2−オキソ−7−(トリフルオロメチル)−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボン酸の製造(製造中間体の化合物番号VIII−33)
(1)エチル 2−アミノ−6−(トリフルオロメチル)ニコチネートの製造
エチル 3−アミノ−3−イミノプロパノエート(ケミカル・アンド・ファーマシューティカル・ビュレティン(Chemical and Pharmaceutical Bulletin)、第43巻、第5号、793頁(1995年)に記載)19.5g(0.12mol)をアセトニトリル100mLに加え、室温下で1,8−ジアザビシクロ[5.4.0]−7−ウンデセン18.6g(0.12mol)を加えて5分撹拌した。この混合物に4−エトキシ−1、1、1−トリフルオロ−3−ブテン−2−オン20.6g(0.12mol)を加え、1,8−ジアザビシクロ[5.4.0]−7−ウンデセン18.6g(0.12mol)を加えて、80℃で3時間撹拌した。反応混合物から溶媒を減圧留去して半分まで濃縮し、氷水を加えた。析出した結晶をろ別し酢酸エチルに溶解させた。ろ液は酢酸エチルで抽出し、結晶を溶解させた溶液と抽出した有機相を合わせ、食塩水で洗浄後、乾燥、濃縮した。残渣をカラムクロマトグラフィー(酢酸エチル:n‐ヘキサン=1:9〜1:4)で精製し無色結晶の標記化合物を17.8g得た(収率62%)。
1.40(3H,s)、4.38(2H,q)、5.5-7.5(2H,br)、6.95(1H,d, J=7.95Hz) 、8.29(1H,d, J=7.95Hz)
エチル 2−アミノ−6−(トリフルオロメチル)ニコチネート5.0g(21mmol)とぎ酸10mLを混合し、100℃で一昼夜加熱撹拌した。反応混合物を冷却後、濃縮し、残渣をカラムクロマトグラフィー(酢酸エチル:n‐ヘキサン=1:9〜4:6)で精製し無色結晶の標記化合物を3.7g得た(収率66%)。
1.44(3H,s)、4.45(2H,q)、7.43(1H,d, J=8.22Hz)、8.50(1H,d, J=7.38Hz)、9.71(1H,d, J=9.87Hz)、10.59 (1H,br)
(3)2−(メチルアミノ)−6−(トリフルオロメチル)−3−ピリジンメタノールの製造
窒素気流下で水素化リチウムアルミニウム1.75g(42mmol)をテトラヒドロフラン(100mL)に加え、エチル 2−ホルムアミド−6−(トリフルオロメチル)ニコチネート3.7g(14mmol)のテトラヒドロフラン(30mL)溶液を滴下し、40℃で2時間撹拌した。反応混合物に、酢酸エチルを加え、続いて10%水酸化ナトリウム水溶液18mLを加え、不溶物をろ過した。ろ液を濃縮し、得られた残渣を酢酸エチルに溶解し、乾燥、ろ過、濃縮して得られた固体をジイソプロピルエーテルで洗浄して淡黄色結晶の標記化合物を2.30g得た(収率79%)。
3.04(3H,d)、4.61(2H,s)、4.56(1H,s)、6.84 (1H,d)、7.27(1H,d)
2−(メチルアミノ)−6−(トリフルオロメチル)−3−ピリジンメタノール2.3g(11mmol)をクロロホルム(100mL)に溶解し、二酸化マンガン3.3g(33mmol)を加えて50℃で8時間撹拌した。反応混合物をろ過し、ろ液を濃縮して残渣をカラムクロマトグラフィー(酢酸エチル:n‐ヘキサン=1:4〜3:7)で精製し黄色固体の標記化合物を1.26g得た(収率55%)。
3.10(3H,d)、6.93 (1H,d)、7.86(1H,d)、8.38(1H,br)、9.88(1H,br)
2−(メチルアミノ)−6−(トリフルオロメチル)−3−ニコチンアルデヒド1.26g(6.2mmol)をエタノール(50mL)に溶解し、マロン酸ジエチル1.5g(9.4mmol)とピロリジン0.3mL(3mmol)を加え100℃で一晩撹拌した。反応混合物を冷却後、濃縮して析出した固体をジイソプロピルエーテルで洗浄して淡黄色固体の標記化合物を1.24g得た(収率67%)。
1.43(3H,t)、3.87(3H,s)、4.44(2H,q)、7.56(1H,d)、8.14(1H,d)、8.35(1H,s)
エチル 1−メチル−2−オキソ−7−(トリフルオロメチル)−1,2−ジヒドロ−1,8−ナフチリジン−3−カルボキシレート1.24g(4.1mmol)を1,4−ジオキサン(50mL)に溶解し、室温下で水酸化リチウム一水和物0.35g(8.3mmol)と水10mLを加え、室温で一晩撹拌した。反応混合物を炭酸水素ナトリウム水溶液にあけ、酢酸エチルで洗浄し、水相をクエン酸で酸性にしてから酢酸エチルで抽出した。有機相を水洗、乾燥、濃縮し、残渣をノルマルヘキサンで洗浄して無色結晶の標記化合物を1.02g得た(収率91%)。
4.01(3H,s)、7.74(1H,d)、8.37(1H,d)、8.96(1H,s)、14.04(1H,s)
次に代表的な製剤例をあげて製剤方法を具体的に説明する。化合物、添加剤の種類及び配合比率は、これのみに限定されることなく広い範囲で変更可能である。以下の説明において「部」は重量部を意味する。
化合物番号II−2の化合物 10部
ポリオキシエチレンオクチルフェニルエーテル 0.5部
β−ナフタレンスルホン酸ホルマリン縮合物ナトリウム塩 0.5部
珪藻土 20部
クレー 69部
以上を均一に混合粉砕して水和剤とした。又、化合物番号II−2に代えて、表1〜66に記載の化合物各々を用いて同様に水和剤を得ることができた。
化合物番号II−41の化合物 20部
水 69部
ポリオキシエチレンスチレン化フェニルエーテル硫酸塩 4部
エチレングリコール 7部
以上にシリコーンAF−118N(旭化成工業株式会社製)を全量に対し200ppm加え、高速攪拌機にて30分間混合した後、湿式粉砕機にて粉砕しフロアブル剤とした。また、化合物番号II−41に代えて、表1〜66に記載の化合物各々を用いて同様にフロアブル剤を得ることができる。
化合物番号III−118の化合物 30部
キシレンとイソホロンの等量混合物 60部
ポリオキシエチレンソルビタンアルキレート 4部
ポリオキシエチレンポリアルキルアリールエーテル 4部
アルキルアリールスルホネート 2部
以上を均一に溶解して乳剤とした。また、化合物番号III−118に代えて、表1〜66に記載の化合物各々を用いて同様に乳剤を得ることができる。
化合物番号IV−41の化合物 10部
タルクとベントナイトの(1:3)混合物 80部
ホワイトカーボン 5部
ポリオキシエチレンソルビタンアルキレート 2部
ポリオキシエチレンポリアルキルアリールエーテル 2部
アルキルアリールスルホネート 1部
以上を均一に混合粉砕した。この混合物に水10部相当量を加えて練合し、押出式造粒機を用いて直径0.7mmのふるい穴から押し出して乾燥した後に0.5〜1mmの長さに切断し、粒剤とした。また、化合物番号IV−41に代えて、表1〜66に記載の化合物各々を用いて同様に粒剤を得ることができる。
〈試験例1〉 水田土壌処理による除草効果試験
100cm2プラスチックポットに水田土壌を充填し、代掻後、タイヌビエ、コナギ、イヌホタルイの種子を播種し、水深3cmに湛水した。翌日、製剤例1に準じて調製した水和剤を水で希釈し、水面滴下した。施用量は、有効成分を、1ヘクタール当り1000g相当とした。その後、温室内で育成し、処理後21日目に次の表71に記載の基準に従って除草効果を調査した。
80cm2プラスチックポットに畑土壌を充填し、イチビ、アオゲイトウの種子を播種して覆土した。製剤例1に準じて調製した水和剤を水で希釈し、1ヘクタール当り有効成分が1000gになるように、1ヘクタール当り1000リットル相当を小型噴霧器で土壌表面に均一に散布した。その後、温室内で育成し、処理21日目に前記した表71に記載の基準に従って、除草効果を調査した。結果を次の表74に示す。
80cm2プラスチックポットに畑土壌を充填し、イヌビエ、イチビ、アオゲイトウの種子を播種し、温室内で2週間育成後、製剤例1に準じて調製した水和剤を水で希釈し、1ヘクタール当り有効成分が1000gになる様に、1ヘクタール当り1000リットル相当を小型噴霧器で植物体の上方から全体に茎葉散布処理した。その後、温室内で育成し、処理14日目に前記した表71に記載の基準に従って、除草効果を調査した。その結果を次の表75に示す。
Claims (3)
- 一般式[I]
X2、X3及びX4は、CH(当該炭素原子はR2により置換されてもよい。);又はN(O)mを表し、
mは、0を表し、
R1は、C 1〜C12アルキル基;C2〜C6アルケニル基;C2〜C6アルキニル基;C3〜C8シクロアルキル基;C3〜C8シクロアルキルC1〜C6アルキル基;C1〜C6ハロアルキル基;C2〜C6ハロアルケニル基;C2〜C6ハロアルキニル基;C3〜C8ハロシクロアルキル基;C3〜C8ハロシクロアルキルC1〜C6アルキル基;アミノC1〜C6アルキル基;ニトロC1〜C6アルキル基;モノ(C1〜C6アルキル)アミノC1〜C6アルキル基;ジ(C1〜C6アルキル)アミノC1〜C6アルキル基;C1〜C6アルキルチオC1〜C6アルキル基;C1〜C6アルキルスルフィニルC1〜C6アルキル基;C1〜C6アルキルスルホニルC1〜C6アルキル基;C1〜C6ハロアルキルチオC1〜C6アルキル基;C1〜C6ハロアルキルスルフィニルC1〜C6アルキル基;C1〜C6ハロアルキルスルホニルC1〜C6アルキル基;C1〜C6アルコキシC1〜C6アルキル基;ヒドロキシC1〜C6アルキル基;フェニルC1〜C6アルコキシC1〜C6アルキル基(該基のフェニルは、1又は2〜5個の同一もしくは異なるR4により置換されてもよい。);C1〜C6アルコキシC1〜C6アルコキシC1〜C6アルキル基;C3〜C8シクロアルキルオキシC1〜C6アルキル基;C3〜C8シクロアルキルC1〜C6アルコキシC1〜C6アルキル基;フェニルオキシC1〜C6アルキル基(該基のフェニルは、1又は2〜5個の同一もしくは異なるR4により置換されてもよい。);酸素原子、硫黄原子及び窒素原子より選択される1〜5個のヘテロ原子を有する炭素数2〜10の複素環オキシC1〜C6アルキル基(該基の酸素原子、硫黄原子及び窒素原子より選択される1〜5個のヘテロ原子を有する炭素数2〜10の複素環は、1又は2〜5個の同一もしくは異なるR5により置換されてもよい。);フェニルチオC1〜C6アルキル基(該基のフェニルは、1又は2〜5個の同一もしくは異なるR4により置換されてもよい。);フェニルスルフィニルC1〜C6アルキル基(該基のフェニルは、1又は2〜5個の同一もしくは異なるR4により置換されてもよい。);フェニルスルホニルC1〜C6アルキル基(該基のフェニルは、1又は2〜5個の同一もしくは異なるR4により置換されてもよい。);C1〜C6ハロアルコキシC1〜C6アルキル基;酸素原子、硫黄原子及び窒素原子より選択される1〜5個のヘテロ原子を有する炭素数2〜10の複素環C1〜C6アルコキシC1〜C6アルキル基(該基の酸素原子、硫黄原子及び窒素原子より選択される1〜5個のヘテロ原子を有する炭素数2〜10の複素環は、1又は2〜5個の同一もしくは異なるR5により置換されてもよい。);C1〜C6アルキルチオC1〜C6アルコキシC1〜C6アルキル基;C1〜C6アルキルスルフィニルC1〜C6アルコキシC1〜C6アルキル基;C1〜C6アルキルスルホニルC1〜C6アルコキシC1〜C6アルキル基;シアノC1〜C6アルコキシC1〜C6アルキル基;シアノC1〜C6アルキル基;C1〜C6アルキルカルボニルオキシC1〜C6アルキル基;C1〜C6アシルC1〜C6アルキル基;ジ(C1〜C6アルコキシ)C1〜C6アルキル基;C1〜C6アルコキシカルボニルC1〜C6アルキル基;C1〜C6アルコキシイミノC1〜C6アルキル基;C1〜C6アルキリデンアミノオキシC1〜C6アルキル基;(R6R7N−C=O)C1〜C6アルキル基;C6〜C10アリールC1〜C6アルキル基(該基のアリールは、1又は2〜5個の同一もしくは異なるR4により置換されてもよい。);酸素原子、硫黄原子及び窒素原子より選択される1〜5個のヘテロ原子を有する炭素数2〜10の複素環C1〜C6アルキル基(該基の酸素原子、硫黄原子及び窒素原子より選択される1〜5個のヘテロ原子を有する炭素数2〜10の複素環は、1又は2〜5個の同一もしくは異なるR5により置換されてもよい。);NR8R9基;C1〜C6アルコキシ基;C6〜C10アリール基(該基は1又は2〜5個の同一もしくは異なるR4により置換されてもよい。);又は、酸素原子、硫黄原子及び窒素原子より選択される1〜5個のヘテロ原子を有する炭素数2〜10の複素環基(該基は、1又は2〜5個の同一もしくは異なるR5により置換されてもよい。)を表し、
R2は、ハロゲン原子;ヒドロキシル基;ニトロ基;シアノ基;C1〜C6アルキル基;C3〜C8シクロアルキル基;C3〜C8シクロアルキルC1〜C6アルキル基;C2〜C6アルケニル基;C2〜C6アルキニル基;C1〜C6ハロアルキル基;C2〜C6ハロアルケニル基;C2〜C6ハロアルキニル基;C3〜C8ハロシクロアルキル基;C3〜C8ハロシクロアルキルC1〜C6アルキル基;C1〜C6アルコキシ基;C3〜C8シクロアルキルオキシ基;C3〜C8シクロアルキルC1〜C6アルキルオキシ基;C2〜C6アルケニルオキシ基;C2〜C6アルキニルオキシ基;C1〜C6ハロアルコキシ基;C1〜C6アルコキシC1〜C6アルコキシ基;C1〜C6アルキルカルボニルオキシ基;C1〜C6アルキルチオ基;C1〜C6アルキルスルフィニル基;C1〜C6アルキルスルホニル基;C1〜C6ハロアルキルチオ基;C1〜C6ハロアルキルスルフィニル基;C1〜C6ハロアルキルスルホニル基;アミノ基;モノ(C1〜C6アルキル)アミノ基;ジ(C1〜C6アルキル)アミノ基;C1〜C6アシルアミノ基;ヒドロキシC1〜C6アルキル基;C1〜C6アルコキシC1〜C6アルキル基;C1〜C6アルキルチオC1〜C6アルキル基;C1〜C6アルキルスルフィニルC1〜C6アルキル基;C1〜C6アルキルスルホニルC1〜C6アルキル基;C1〜C6ハロアルキルチオC1〜C6アルキル基;C1〜C6ハロアルキルスルフィニルC1〜C6アルキル基;C1〜C6ハロアルキルスルホニルC1〜C6アルキル基;シアノC1〜C6アルキル基;C1〜C6アシル基;C1〜C6アルコキシイミノC1〜C6アルキル基;カルボキシル基;C1〜C6アルコキシカルボニル基;カルバモイル基;モノ(C1〜C6アルキル)アミノカルボニル基;ジ(C1〜C6アルキル)アミノカルボニル基;又は、酸素原子、硫黄原子及び窒素原子より選択される1〜5個のヘテロ原子を有する炭素数2〜10の複素環基(該基の酸素原子、硫黄原子及び窒素原子より選択される1〜5個のヘテロ原子を有する炭素数2〜10の複素環は、1又は2〜5個の同一もしくは異なるR10により置換されてもよい。)を表し、
また、R2は、隣接した2個のR2が一緒になって、それぞれのR2が直接結合している炭素原子と共に、炭素環又は酸素原子、硫黄原子及び窒素原子より選択される1〜4個のヘテロ原子を有する複素環である4〜8員環を形成してもよく、このときに形成された環はハロゲン原子;シアノ基;ニトロ基;C1〜C6アルキル基;C1〜C6ハロアルキル基;C1〜C6アルコキシ基;C1〜C6ハロアルコキシ基;又はオキソ基で置換されてもよく、
nは、X2、X3及びX4がCH(該炭素原子はR2により置換されてもよい。)、即ち、置換基R2により置換されてもよいCHである場合は0〜4の整数を表し、
R3は、ヒドロキシル基;又はO−M+(M+はアルカリ金属カチオン又はアンモニウムカチオンを示す。)を表し、
R4は、ハロゲン原子;ヒドロキシル基;ニトロ基;シアノ基;C1〜C6アルキル基;C3〜C8シクロアルキル基;C3〜C8シクロアルキルC1〜C6アルキル基;C2〜C6アルケニル基;C2〜C6アルキニル基;C1〜C6ハロアルキル基;C2〜C6ハロアルケニル基;C2〜C6ハロアルキニル基;C3〜C8ハロシクロアルキル基;、C3〜C8ハロシクロアルキルC1〜C6アルキル基;C1〜C6アルコキシ基;C3〜C8シクロアルキルオキシ基;C2〜C6アルケニルオキシ基;C2〜C6アルキニルオキシ基;C1〜C6アルキルカルボニルオキシ基;C1〜C6ハロアルコキシ基;C1〜C6アルキルチオ基;C1〜C6アルキルスルフィニル基;C1〜C6アルキルスルホニル基;C1〜C6ハロアルキルチオ基;C1〜C6ハロアルキルスルフィニル基;C1〜C6ハロアルキルスルホニル基;アミノ基;C1〜C6アシルアミノ基;モノ(C1〜C6アルキル)アミノ基;ジ(C1〜C6アルキル)アミノ基;ヒドロキシC1〜C6アルキル基;C1〜C6アルコキシC1〜C6アルキル基;C1〜C6アルキルチオC1〜C6アルキル基;C1〜C6アルキルスルフィニルC1〜C6アルキル基;C1〜C6アルキルスルホニルC1〜C6アルキル基;C1〜C6ハロアルキルチオC1〜C6アルキル基;C1〜C6ハロアルキルスルフィニルC1〜C6アルキル基;C1〜C6ハロアルキルスルホニルC1〜C6アルキル基;シアノC1〜C6アルキル基;C1〜C6アルコキシC1〜C6アルコキシ基;C3〜C8シクロアルキルC1〜C6アルキルオキシ基;C1〜C6ハロアルコキシC1〜C6アルコキシ基;シアノC1〜C6アルコキシ基;C1〜C6アシル基;C1〜C6アルコキシイミノC1〜C6アルキル基;カルボキシル基;C1〜C6アルコキシカルボニル基;カルバモイル基;モノ(C1〜C6アルキル)アミノカルボニル基;ジ(C1〜C6アルキル)アミノカルボニル基;酸素原子、硫黄原子及び窒素原子より選択される1〜5個のヘテロ原子を有する炭素数2〜10の複素環基(該基の複素環は、1又は2〜5個の同一もしくは異なるR10により置換されてもよい。);
又は、酸素原子、硫黄原子及び窒素原子より任意に選択される1〜5個のヘテロ原子を有する炭素数2〜10の複素環オキシ基(該基の酸素原子、硫黄原子及び窒素原子より選択される1〜5個のヘテロ原子を有する炭素数2〜10の複素環は、1又は2〜5個の同一もしくは異なるR10により置換されてもよい。)を表し、
また、R4は、隣接した2個のR4が一緒になって、それぞれのR4が直接結合している炭素原子と共に、炭素環又は酸素原子、硫黄原子及び窒素原子より選択される1〜4個のヘテロ原子を有する複素環である4〜8員環を形成してもよく、このときに形成された環はハロゲン原子;シアノ基;ニトロ基;C1〜C6アルキル基;C1〜C6ハロアルキル基;C1〜C6アルコキシ基;C1〜C6ハロアルコキシ基;又はオキソ基で置換されてもよく、
R5は、オキソ基;チオキソ基;ヒドロキシル基;ハロゲン原子;ニトロ基;シアノ基;C1〜C6アルキル基;C2〜C6アルケニル基;C2〜C6アルキニル基;C3〜C8シクロアルキル基;C3〜C8シクロアルキルC1〜C6アルキル基;C1〜C6ハロアルキル基;C2〜C6ハロアルケニル基;C3〜C8ハロシクロアルキル基;C3〜C8ハロシクロアルキルC1〜C6アルキル基;C1〜C6アルコキシ基;C2〜C6アルケニルオキシ基;C2〜C6アルキニルオキシ基;C3〜C8シクロアルキルオキシ基;C3〜C8シクロアルキルC1〜C6アルキルオキシ基;C1〜C6ハロアルコキシ基;C1〜C6アルコキシC1〜C6アルコキシ基;C1〜C6ハロアルコキシC1〜C6アルコキシ基;シアノC1〜C6アルコキシ基;C1〜C6アルキルカルボニルオキシ基;C1〜C6アルキルチオ基;C1〜C6アルキルスルフィニル基;C1〜C6アルキルスルホニル基;C1〜C6ハロアルキルチオ基;C1〜C6ハロアルキルスルフィニル基;C1〜C6ハロアルキルスルホニル基;アミノ基;モノ(C1〜C6アルキル)アミノ基;ジ(C1〜C6アルキル)アミノ基;C1〜C6アシルアミノ基;カルボキシル基;C1〜C6アルコキシカルボニル基;カルバモイル基;モノ(C1〜C6アルキル)アミノカルボニル基;ジ(C1〜C6アルキル)アミノカルボニル基;C1〜C6アシル基;C1〜C6アルコキシイミノC1〜C6アルキル基;C1〜C6アルコキシC1〜C6アルキル基;C1〜C6アルキルチオC1〜C6アルキル基;C1〜C6アルキルスルフィニルC1〜C6アルキル基;C1〜C6アルキルスルホニルC1〜C6アルキル基;C1〜C6ハロアルキルチオC1〜C6アルキル基;C1〜C6ハロアルキルスルフィニルC1〜C6アルキル基;C1〜C6ハロアルキルスルホニルC1〜C6アルキル基;又はシアノC1〜C6アルキル基を表し、
また、R5は、隣接した2個のR5が一緒になって、それぞれのR5が直接結合している炭素原子と共に、炭素環又は酸素原子、硫黄原子及び窒素原子より選択される1〜4個のヘテロ原子を有する複素環である4〜8員環を形成してもよく、このときに形成された環はハロゲン原子;シアノ基;ニトロ基;C1〜C6アルキル基;C1〜C6ハロアルキル基;C1〜C6アルコキシ基;C1〜C6ハロアルコキシ基;又はオキソ基で置換されてもよく、
R6及びR7は、互いに独立して、C1〜C6アルキル基;又はフェニルC1〜C6アルキルオキシカルボニル基を表し、
また、R6及びR7は、これらが一緒になってこれらが結合している窒素原子と共に5〜6員環を形成していてもよく、このときに形成された環中にR6及びR7が結合している窒素原子以外に酸素原子が介在していてもよく、
R8及びR9は、互いに独立して、水素原子;C1〜C6アルキル基;NR6R7基;又はC1〜C6アルコキシカルボニル基を表し、
また、R8及びR9は、これらが一緒になってこれらが結合している窒素原子と共に5〜6員環を形成していてもよく、この際、この環中にR8及びR9が結合している窒素原子以外に硫黄原子及び/又は酸素原子が介在していてもよく、
R10は、ハロゲン原子;ニトロ基;シアノ基;C1〜C6アルキル基;C1〜C6ハロアルキル基;C1〜C6アルコキシ基;又はC1〜C6ハロアルコキシ基を表し、
A1は、C(R11R12)を表し、
A2は、C(R13R14)、又はC=Oを表し、
A3は、C(R15R16)を表し、
R11、R12、R13、R14、R15及びR16は、互いに独立して、水素原子;又はC1〜C6アルキル基を表し、
また、R11とR16はこれらが一緒になってC2〜C5アルキレン鎖を形成し、隣接する炭素原子と共に環を構成しても良い。}で表される2−ピリドン誘導体又はその農薬上許容される塩。 - 請求項1に記載の2−ピリドン誘導体又はその塩を活性成分として含有することを特徴とする除草剤。
- 請求項2に記載の除草剤の有効量を土壌及び/又は植物に処理することを特徴とする除草剤の使用。
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US8334236B2 (en) | 2012-12-18 |
JPWO2010089993A1 (ja) | 2012-08-09 |
EP2394995A4 (en) | 2012-06-27 |
US20110287937A1 (en) | 2011-11-24 |
EP2394995B1 (en) | 2014-01-15 |
WO2010089993A1 (ja) | 2010-08-12 |
EP2394995A1 (en) | 2011-12-14 |
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