JP3953494B2 - アルキルスルホニルトリアゾール誘導体およびその製造方法 - Google Patents
アルキルスルホニルトリアゾール誘導体およびその製造方法 Download PDFInfo
- Publication number
- JP3953494B2 JP3953494B2 JP2005208848A JP2005208848A JP3953494B2 JP 3953494 B2 JP3953494 B2 JP 3953494B2 JP 2005208848 A JP2005208848 A JP 2005208848A JP 2005208848 A JP2005208848 A JP 2005208848A JP 3953494 B2 JP3953494 B2 JP 3953494B2
- Authority
- JP
- Japan
- Prior art keywords
- methyl
- alkyl
- ethyl
- substituted
- cyano
- 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.)
- Expired - Fee Related
Links
- 238000004519 manufacturing process Methods 0.000 title description 14
- -1 cyano, methoxy Chemical group 0.000 claims description 20
- 125000000217 alkyl group Chemical group 0.000 claims description 16
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 15
- 239000000460 chlorine Chemical group 0.000 claims description 15
- 229910052801 chlorine Inorganic materials 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 15
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 14
- 238000006243 chemical reaction Methods 0.000 claims description 13
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 13
- 229910052731 fluorine Inorganic materials 0.000 claims description 13
- 239000011737 fluorine Substances 0.000 claims description 13
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 12
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 10
- 125000001153 fluoro group Chemical group F* 0.000 claims description 10
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 10
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 9
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 9
- 229910052794 bromium Inorganic materials 0.000 claims description 9
- 229910052736 halogen Inorganic materials 0.000 claims description 9
- 150000002367 halogens Chemical class 0.000 claims description 9
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 9
- 125000003545 alkoxy group Chemical group 0.000 claims description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 7
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 6
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 6
- 125000003342 alkenyl group Chemical group 0.000 claims description 5
- 125000000304 alkynyl group Chemical group 0.000 claims description 5
- KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 claims description 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 4
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 4
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 4
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 claims description 4
- 239000003085 diluting agent Substances 0.000 claims description 4
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 4
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 4
- 239000007800 oxidant agent Substances 0.000 claims description 4
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 4
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 3
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 3
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 2
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims description 2
- LJGHYPLBDBRCRZ-UHFFFAOYSA-N 3-(3-aminophenyl)sulfonylaniline Chemical compound NC1=CC=CC(S(=O)(=O)C=2C=C(N)C=CC=2)=C1 LJGHYPLBDBRCRZ-UHFFFAOYSA-N 0.000 claims description 2
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 claims description 2
- 239000005708 Sodium hypochlorite Substances 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 2
- 125000001664 diethylamino group Chemical group [H]C([H])([H])C([H])([H])N(*)C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims description 2
- 125000000031 ethylamino group Chemical group [H]C([H])([H])C([H])([H])N([H])[*] 0.000 claims description 2
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 claims description 2
- 230000001590 oxidative effect Effects 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 239000012286 potassium permanganate Substances 0.000 claims description 2
- CZPZWMPYEINMCF-UHFFFAOYSA-N propaneperoxoic acid Chemical compound CCC(=O)OO CZPZWMPYEINMCF-UHFFFAOYSA-N 0.000 claims description 2
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 claims description 2
- 125000003944 tolyl group Chemical group 0.000 claims description 2
- YNJSNEKCXVFDKW-UHFFFAOYSA-N 3-(5-amino-1h-indol-3-yl)-2-azaniumylpropanoate Chemical compound C1=C(N)C=C2C(CC(N)C(O)=O)=CNC2=C1 YNJSNEKCXVFDKW-UHFFFAOYSA-N 0.000 claims 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 1
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 30
- 150000001875 compounds Chemical class 0.000 description 27
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 18
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- 239000000203 mixture Substances 0.000 description 13
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 12
- 239000000243 solution Substances 0.000 description 11
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 10
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 9
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 8
- 238000002844 melting Methods 0.000 description 8
- 230000008018 melting Effects 0.000 description 8
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 7
- 239000012074 organic phase Substances 0.000 description 7
- 238000003756 stirring Methods 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 5
- 239000005457 ice water Substances 0.000 description 5
- 239000002243 precursor Substances 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 229910052938 sodium sulfate Inorganic materials 0.000 description 5
- 235000011152 sodium sulphate Nutrition 0.000 description 5
- 239000007858 starting material Substances 0.000 description 5
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 4
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 4
- 239000000706 filtrate Substances 0.000 description 4
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- 238000010992 reflux Methods 0.000 description 4
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 3
- OBKUFPKPQLWJHJ-UHFFFAOYSA-N 4-methyl-3-(trifluoromethyl)-1h-1,2,4-triazol-5-one Chemical compound CN1C(C(F)(F)F)=NNC1=O OBKUFPKPQLWJHJ-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 3
- 241001061127 Thione Species 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 3
- 125000003282 alkyl amino group Chemical group 0.000 description 3
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 description 3
- 238000004821 distillation Methods 0.000 description 3
- 235000019253 formic acid Nutrition 0.000 description 3
- 239000000543 intermediate Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 3
- NWZSZGALRFJKBT-KNIFDHDWSA-N (2s)-2,6-diaminohexanoic acid;(2s)-2-hydroxybutanedioic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O.NCCCC[C@H](N)C(O)=O NWZSZGALRFJKBT-KNIFDHDWSA-N 0.000 description 2
- WNWOTMKHOLCHRJ-UHFFFAOYSA-N 1,4-dihydrotriazol-5-one Chemical class O=C1CN=NN1 WNWOTMKHOLCHRJ-UHFFFAOYSA-N 0.000 description 2
- SKYYTGUCWARUCL-UHFFFAOYSA-N 1-amino-3-ethylthiourea Chemical compound CCNC(=S)NN SKYYTGUCWARUCL-UHFFFAOYSA-N 0.000 description 2
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 2
- WLBHJYWCTKJRBF-UHFFFAOYSA-N 4-ethyl-3-methylsulfanyl-5-(trifluoromethyl)-1,2,4-triazole Chemical compound CCN1C(SC)=NN=C1C(F)(F)F WLBHJYWCTKJRBF-UHFFFAOYSA-N 0.000 description 2
- WQHOWJPICVQSTM-UHFFFAOYSA-N 4-ethyl-3-methylsulfonyl-5-(trifluoromethyl)-1,2,4-triazole Chemical compound CCN1C(C(F)(F)F)=NN=C1S(C)(=O)=O WQHOWJPICVQSTM-UHFFFAOYSA-N 0.000 description 2
- HUZASKHMPBJXJP-UHFFFAOYSA-N 4-methyl-3-(trifluoromethyl)-1h-1,2,4-triazole-5-thione Chemical compound CN1C(C(F)(F)F)=NNC1=S HUZASKHMPBJXJP-UHFFFAOYSA-N 0.000 description 2
- RKNRZDUBPDCHPD-UHFFFAOYSA-N 4-methyl-3-methylsulfanyl-5-(trifluoromethyl)-1,2,4-triazole Chemical compound CSC1=NN=C(C(F)(F)F)N1C RKNRZDUBPDCHPD-UHFFFAOYSA-N 0.000 description 2
- SPZSOFGNLMBWOR-UHFFFAOYSA-N 4-methyl-3-methylsulfonyl-5-(trifluoromethyl)-1,2,4-triazole Chemical compound CN1C(C(F)(F)F)=NN=C1S(C)(=O)=O SPZSOFGNLMBWOR-UHFFFAOYSA-N 0.000 description 2
- PTVZQOAHCSKAAS-UHFFFAOYSA-N 4-methyl-3-thiosemicarbazide Chemical compound CNC(=S)NN PTVZQOAHCSKAAS-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- LGDSHSYDSCRFAB-UHFFFAOYSA-N Methyl isothiocyanate Chemical compound CN=C=S LGDSHSYDSCRFAB-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 235000011054 acetic acid Nutrition 0.000 description 2
- 239000002168 alkylating agent Substances 0.000 description 2
- 229940100198 alkylating agent Drugs 0.000 description 2
- GZUXJHMPEANEGY-UHFFFAOYSA-N bromomethane Chemical compound BrC GZUXJHMPEANEGY-UHFFFAOYSA-N 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 238000004440 column chromatography Methods 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- HBNYJWAFDZLWRS-UHFFFAOYSA-N ethyl isothiocyanate Chemical compound CCN=C=S HBNYJWAFDZLWRS-UHFFFAOYSA-N 0.000 description 2
- IKDUDTNKRLTJSI-UHFFFAOYSA-N hydrazine monohydrate Substances O.NN IKDUDTNKRLTJSI-UHFFFAOYSA-N 0.000 description 2
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 2
- 235000019341 magnesium sulphate Nutrition 0.000 description 2
- 229910000000 metal hydroxide Inorganic materials 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 125000000547 substituted alkyl group Chemical group 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- 0 *C1=**=*(*)CC1 Chemical compound *C1=**=*(*)CC1 0.000 description 1
- LZDKZFUFMNSQCJ-UHFFFAOYSA-N 1,2-diethoxyethane Chemical compound CCOCCOCC LZDKZFUFMNSQCJ-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 1
- BSJUQGMWGJKWIR-UHFFFAOYSA-N 1-methyl-3-[(2,2,2-trifluoroacetyl)amino]urea Chemical compound CNC(=O)NNC(=O)C(F)(F)F BSJUQGMWGJKWIR-UHFFFAOYSA-N 0.000 description 1
- SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- NCEIQKYDNCTJJZ-UHFFFAOYSA-N 3-(difluoromethyl)-4-methyl-5-methylsulfonyl-1,2,4-triazole Chemical compound CN1C(C(F)F)=NN=C1S(C)(=O)=O NCEIQKYDNCTJJZ-UHFFFAOYSA-N 0.000 description 1
- BOBMLXIVWLATRN-UHFFFAOYSA-N 4-ethyl-3-(trifluoromethyl)-1h-1,2,4-triazol-5-one Chemical compound CCN1C(C(F)(F)F)=NNC1=O BOBMLXIVWLATRN-UHFFFAOYSA-N 0.000 description 1
- VOBWXEYGDSSTAW-UHFFFAOYSA-N 4-ethyl-3-(trifluoromethyl)-1h-1,2,4-triazole-5-thione Chemical compound CCN1C(S)=NN=C1C(F)(F)F VOBWXEYGDSSTAW-UHFFFAOYSA-N 0.000 description 1
- QCZIPYDYWLAZQQ-UHFFFAOYSA-N 4-methyl-5-methylsulfanyl-3-(trifluoromethyl)-1,5-dihydro-1,2,4-triazole Chemical compound CSC1NN=C(C(F)(F)F)N1C QCZIPYDYWLAZQQ-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
- 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 1
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- 241001024304 Mino Species 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- OKJPEAGHQZHRQV-UHFFFAOYSA-N Triiodomethane Natural products IC(I)I OKJPEAGHQZHRQV-UHFFFAOYSA-N 0.000 description 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000004414 alkyl thio group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000011609 ammonium molybdate Substances 0.000 description 1
- APUPEJJSWDHEBO-UHFFFAOYSA-P ammonium molybdate Chemical compound [NH4+].[NH4+].[O-][Mo]([O-])(=O)=O APUPEJJSWDHEBO-UHFFFAOYSA-P 0.000 description 1
- 235000018660 ammonium molybdate Nutrition 0.000 description 1
- 229940010552 ammonium molybdate Drugs 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- RDHPKYGYEGBMSE-UHFFFAOYSA-N bromoethane Chemical compound CCBr RDHPKYGYEGBMSE-UHFFFAOYSA-N 0.000 description 1
- 229950005499 carbon tetrachloride Drugs 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 description 1
- 229940117389 dichlorobenzene Drugs 0.000 description 1
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
- 229940075557 diethylene glycol monoethyl ether Drugs 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 229960005437 etoperidone Drugs 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical group II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- HVTICUPFWKNHNG-UHFFFAOYSA-N iodoethane Chemical compound CCI HVTICUPFWKNHNG-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229940102396 methyl bromide Drugs 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229940079827 sodium hydrogen sulfite Drugs 0.000 description 1
- 239000011684 sodium molybdate Substances 0.000 description 1
- 235000015393 sodium molybdate Nutrition 0.000 description 1
- TVXXNOYZHKPKGW-UHFFFAOYSA-N sodium molybdate (anhydrous) Chemical compound [Na+].[Na+].[O-][Mo]([O-])(=O)=O TVXXNOYZHKPKGW-UHFFFAOYSA-N 0.000 description 1
- XMVONEAAOPAGAO-UHFFFAOYSA-N sodium tungstate Chemical compound [Na+].[Na+].[O-][W]([O-])(=O)=O XMVONEAAOPAGAO-UHFFFAOYSA-N 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000000967 suction filtration Methods 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- LSGOVYNHVSXFFJ-UHFFFAOYSA-N vanadate(3-) Chemical compound [O-][V]([O-])([O-])=O LSGOVYNHVSXFFJ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles 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
- C07D249/12—Oxygen or sulfur atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Description
一般式(I)
のトリアゾリノンの製造方法に関するものであって、その方法は、一般式(II)
のアルキルスルホニルトリアゾール誘導体を、温度0〜100℃、大気圧下で、アルカリ金属水酸化物の水溶液と反応させ、その生成物を酸性化し、次いで、常法により採取することを特徴とする。
<発明の詳細な記述>
本発明に関する式(I)の化合物は、次の場合のものである:
式中、R1は、ハロゲン、シアノもしくはC1−C4−アルコキシによって任意に置換されている1〜6個の炭素原子を有するアルキルを表すか、またはハロゲン、シアノもしくはC1−C4−アルキルによって任意に置換されている3〜6個の炭素原子を有するシクロアルキルを表し、そしてR2は、アミノを表すか、または、各々が、アルキル、アルケニルもしくはアルキニル基において6個までの炭素原子を有し、そして各々が、ハロゲン、シアノもしくはC1−C4−アルコキシによって任意に置換されているアルキル、アルケニル、アルキニル、アルコキシ、アルキルアミノもしくはジアルキルアミノを表すか、または、各々が、ハロゲン、シアノ、C1−C4−アルキル、C1−C4−アルコキシもしくはC1−C4−アルコキシ−カルボニルによって任意に置換されているC3−C6−シクロアルキル、C3−C6−シクロアルキル−C1−C2−アルキルもしくはフェニルを表す。
式中、R1が、各々が、フッ素、塩素、臭素、シアノ、メトキシもしくはエトキシによって任意に置換されているメチル、エチル、n−もしくはi−プロピルまたはn−、i−もしくはs−ブチルを表すか、または各々が、フッ素、塩素、臭素、シアノもしくはメチルによって任意に置換されているシクロプロピル、シクロプロピルメチル、シクロブチル、シクロペンチルもしくはシクロヘキシルを表し、そしてR2が、アミノを表すか、または、各々が、フッ素、塩素、シアノ、メトキシもしくはエトキシによって任意に置換されているメチル、エチル、n−もしくはi−プロピル、n−、i−もしくはs−ブチル、アリル、プロパルギル、メトキシ、エトキシ、n−もしくはi−プロポキシ、n−、i−もしくはs−ブトキシ、メチルアミノ、エチルアミノ、n−もしくはi−プロピルアミノ、n−、i−もしくはs−ブチルアミノ、ジメチルアミノまたはジエチルアミノを表すか、または各々が、フッ素、塩素、臭素、シアノ、メチル、エチル、n−もしくはi−プロピル、メトキシ−カルボニルもしくはエトキシ−カルボニルによって任意に置換されているシクロプロピル、シクロブチル、シクロペンチル、シクロヘキシルもしくはフェニルを表す
。
式中、R1が、各々が、フッ素および/または塩素により、任意にモノ、ジ、トリ、テトラ、ペンタ、ヘキサもしくはヘプタ置換されているメチル、エチル、n−もしくはi−プロピル、シクロプロピルもしくはシクロプロピルメチルを表し、そしてR2が、メチル、エチル、n−もしくはi−プロピル、メトキシ、エトキシ、メチルアミノ、エチルアミノ、ジメチルアミノ,シクロプロピル、フェニルもしくはトリルを表す。
のアルキルチオトリアゾール誘導体が、温度0〜100℃で、必要ならば反応補助剤の存
在で、そして必要ならば希釈剤の存在下でオキシダントと反応する場合に得られる(製造実施例、参照)。
のトリアゾリンチオンが、温度0〜100℃で、必要ならば、例えば水酸化ナトリウムもしくは水酸化カリウムのような酸受容体の存在下で、そして必要ならば、例えばメタノールもしくはエタノールのような希釈剤の存在下で、例えば、臭化メチル、ヨウ化メチル、臭化エチルもしくはヨウ化エチルのようなアルキル化剤と反応する場合に得られる(製造実施例、参照)。
方法によって製造することができる(米国特許第3719686号および米国特許第3780052号参照)。
R1−CO−X (V)
[式中、R1は、前記意味を有し、Xは、ヒドロキシルもしくはハロゲンを表す]のカルボン酸が、一般式(VI)
R2−NH−CS−NH−NH2 (VI)
[式中、R2は、前記意味を有する]
のアルキルチオセミカルバジドと、温度0〜100℃で反応する場合に得られる(製造実施例、参照)。
(例1)
(例(II−1))
(例(III−1))
同様にして製造される式(III)の化合物のその他の製造例は、以下の表3に挙げられるものである。
(例(IV−1))
℃に上昇する。還流温度で1時間後、生成する反応水を、還流条件下で3時間かけて水分離器により除去する。反応終了後、反応混合液を濃縮する。
(例(VI−1))
Claims (5)
- 一般式(II)
R2 はアミノを表すか、またはR 2 はアルキル、アルケニル、アルキニル、アルコキシ、アルキルアミノもしくはジアルキルアミノ基を表し、これらの各基はアルキル、アルケニルもしくはアルキニルにおいて6個以下の炭素原子を有しており、そしてこれらの各基は、ハロゲン、シアノもしくはC 1 −C 4 アルコキシにより置換されていてもよく、またはR2はC 3 −C 6 シクロアルキル、C 3 −C 6 シクロアルキル−C 1 −C 4 アルキルまたはフェニルを表し、これらの各基はハロゲン、シアノ、C 1 −C 4 アルキル、C 1 −C 4 アルコキシもしくはC 1 −C 4 アルコキシカルボニルにより置換されていてもよく、そして
R3は、炭素原子1〜4個のアルキルを表す]
のアルキルスルホニルトリアゾール誘導体。 - R 1 が、メチル、エチル、n−もしくはi−プロピルまたはn−,i−もしくはs―ブチルを表し、これらの各基はフッ素、塩素、臭素、シアノ、メトキシもしくはエトキシにより置換されていてもよく、またはR 1 が、シクロプロピル、シクロプロピルメチル、シクロクロブチル、シクロペンチルもしくはシクロヘキシルを表し、こらの各基はフッ素、塩素、臭素、シアノもしくはメチルにより置換されていてもよく、
R 2 がアミノを表すか、またはR 2 がメチル、エチル、n−もしくはi−プロピル、n−,i−もしくはs―ブチル、アリル、プロパギル、メトキシ、エトキシ、n−もしくはi−プロポキシ、n−、i−もしくはs−ブトキシ、メチルアミノ、エチルアミノ、n−もしくはi−プロピルアミノ、n−、i−もしくはs−ブチルアミノ、ジメチルアミノまたはジエチルアミノを表し、これらの各基はフッ素、塩素、臭素、シアノ、メトキシもしくはエトキシにより置換されていてもよく、またはR 3 がシクロプロピル、シクロブチル、シクロペンチル、シクロヘキシルもしくはフェニルを表し、これらの各基はフッ素、塩素、臭素、シアノ、メチル、エチル、n−もしくはi−プロピル、メトキシカルボニルまたはエトキシカルボニルにより置換されていてもよく、そして
R 3 がメチルまたはエチルを表す、請求項1記載のアルキルスルホニルトリアゾール誘導体。 - R 1 がメチル、エチル、n−もしくはi−プロピル、シクロプロピルまたはシクロプロピルメチルを表し、これらの各基は、適する場合には、フッ素もしくは塩素によりモノ、ジ、トリ、テトラ、ペンタ、ヘキサもしくはヘプタ置換されており、
R 2 がメチル、エチル、n−もしくはi−プロピル、メトキシ、エトキシ、メチルアミノ、エチルアミノ、ジメチルアミノ、シクロプロピル、フェニルまたはトリルを表し、そして
R 3 がメチルまたはエチルを表す、請求項1記載のアルキルスルホニルトリアゾール誘導体。 - 酸化剤が、酸素、オゾン、過酸化水素、塩素、次亜塩素酸ナトリウム液、過マンガン酸カリウム、過ギ酸、過酢酸、過プロピオン酸およびハロゲン化されていてもよい過安息香酸からなる群より選ばれる請求項4記載の方法。
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE4339412A DE4339412A1 (de) | 1993-11-18 | 1993-11-18 | Verfahren und neue Zwischenprodukte zur Herstellung von Triazolinonen |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP30269794A Division JP3775755B2 (ja) | 1993-11-18 | 1994-11-14 | トリアゾリノン製造のための方法および新規中間体 |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2006221149A Division JP2006342179A (ja) | 1993-11-18 | 2006-08-14 | アルキルチオトリアゾール誘導体およびその製造方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2006001937A JP2006001937A (ja) | 2006-01-05 |
JP3953494B2 true JP3953494B2 (ja) | 2007-08-08 |
Family
ID=6502913
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP30269794A Expired - Fee Related JP3775755B2 (ja) | 1993-11-18 | 1994-11-14 | トリアゾリノン製造のための方法および新規中間体 |
JP2005208848A Expired - Fee Related JP3953494B2 (ja) | 1993-11-18 | 2005-07-19 | アルキルスルホニルトリアゾール誘導体およびその製造方法 |
JP2006221149A Pending JP2006342179A (ja) | 1993-11-18 | 2006-08-14 | アルキルチオトリアゾール誘導体およびその製造方法 |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP30269794A Expired - Fee Related JP3775755B2 (ja) | 1993-11-18 | 1994-11-14 | トリアゾリノン製造のための方法および新規中間体 |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2006221149A Pending JP2006342179A (ja) | 1993-11-18 | 2006-08-14 | アルキルチオトリアゾール誘導体およびその製造方法 |
Country Status (6)
Country | Link |
---|---|
US (3) | US5475115A (ja) |
EP (1) | EP0661277B1 (ja) |
JP (3) | JP3775755B2 (ja) |
KR (1) | KR100344116B1 (ja) |
DE (2) | DE4339412A1 (ja) |
ES (1) | ES2114115T3 (ja) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6344587B1 (en) | 1997-10-08 | 2002-02-05 | Bayer Aktiengesellschaft | Method for producing triazolinthion derivatives |
DE19744400A1 (de) * | 1997-10-08 | 1999-04-15 | Bayer Ag | Verfahren zur Herstellung von Triazolinthion-Derivaten |
FR2787794B1 (fr) * | 1998-12-29 | 2004-09-10 | Atochem Elf Sa | Polymeres a base de chlorure de vinyle, aptes a donner des plastisols de proprietes particulieres et leur procede d'obtention |
JP2002053561A (ja) * | 1999-12-08 | 2002-02-19 | Sumitomo Chem Co Ltd | ジフルオロメチルトリアゾロン化合物、その用途およびその製造中間体 |
US6472535B1 (en) | 2001-10-02 | 2002-10-29 | Bayer Corporation | Oxidative hydrolysis of heteroaromatic thiones |
US6541667B1 (en) | 2001-12-17 | 2003-04-01 | Bayer Corporation | Methods for preparation of thioamides |
US7976898B2 (en) | 2006-09-20 | 2011-07-12 | Asm Genitech Korea Ltd. | Atomic layer deposition apparatus |
WO2014202510A1 (de) | 2013-06-20 | 2014-12-24 | Bayer Cropscience Ag | Arylsulfid- und arylsulfoxid-derivate als akarizide und insektizide |
EP3210469A1 (de) | 2016-02-23 | 2017-08-30 | Bayer Cropscience AG | Verwendung von substituierten thio-1,2,4-triazolen zur steigerung der stresstoleranz in pflanzen |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4120864A (en) * | 1970-08-26 | 1978-10-17 | Rohm And Haas Company | 1,2,4-4H-triazole derivatives |
US3780052A (en) * | 1972-07-19 | 1973-12-18 | Lilly Co Eli | Triazoline phosphates |
ATE4422T1 (de) * | 1979-10-18 | 1983-08-15 | Warner-Lambert Company | Substituierte 5-((7-chlor-4-chinolinyl)amino)-3(aminomethyl)-(1,1'-biphenyl)-2-ol-verbindungen verfahren zu ihrer herstellung; und die verbindungen enthaltende pharmazeutische zusammensetzungen. |
DE3332271A1 (de) * | 1983-09-07 | 1985-03-21 | Bayer Ag, 5090 Leverkusen | Herbizide mittel enthaltend metribuzin in kombination mit substituierten azolyl-derivaten |
US4900743A (en) * | 1987-01-27 | 1990-02-13 | Merrell Dow Pharmaceuticals Inc. | 3-aryl-5-alkylthio-4H-1,2,4-triazoles |
IE903395A1 (en) * | 1989-09-26 | 1991-04-10 | Takeda Chemical Industries Ltd | Triazole compounds, their production and use |
AU644500B2 (en) * | 1990-12-20 | 1993-12-09 | Merrell Dow Pharmaceuticals Inc. | 3-aryl-5-alkylthio-4h-1,2,4-triazoles for treatment of hyperreflexia due to spinal trauma |
-
1993
- 1993-11-18 DE DE4339412A patent/DE4339412A1/de not_active Withdrawn
-
1994
- 1994-11-07 DE DE59405426T patent/DE59405426D1/de not_active Expired - Fee Related
- 1994-11-07 ES ES94117519T patent/ES2114115T3/es not_active Expired - Lifetime
- 1994-11-07 EP EP94117519A patent/EP0661277B1/de not_active Expired - Lifetime
- 1994-11-10 US US08/336,943 patent/US5475115A/en not_active Expired - Lifetime
- 1994-11-14 KR KR1019940029831A patent/KR100344116B1/ko not_active IP Right Cessation
- 1994-11-14 JP JP30269794A patent/JP3775755B2/ja not_active Expired - Fee Related
-
1995
- 1995-09-14 US US08/528,375 patent/US5639891A/en not_active Expired - Lifetime
-
1997
- 1997-01-21 US US08/784,653 patent/US5739349A/en not_active Expired - Fee Related
-
2005
- 2005-07-19 JP JP2005208848A patent/JP3953494B2/ja not_active Expired - Fee Related
-
2006
- 2006-08-14 JP JP2006221149A patent/JP2006342179A/ja active Pending
Also Published As
Publication number | Publication date |
---|---|
JPH07188186A (ja) | 1995-07-25 |
EP0661277A1 (de) | 1995-07-05 |
EP0661277B1 (de) | 1998-03-11 |
DE59405426D1 (de) | 1998-04-16 |
DE4339412A1 (de) | 1995-05-24 |
KR950014082A (ko) | 1995-06-15 |
US5639891A (en) | 1997-06-17 |
JP2006001937A (ja) | 2006-01-05 |
US5475115A (en) | 1995-12-12 |
KR100344116B1 (ko) | 2002-11-29 |
US5739349A (en) | 1998-04-14 |
JP3775755B2 (ja) | 2006-05-17 |
ES2114115T3 (es) | 1998-05-16 |
JP2006342179A (ja) | 2006-12-21 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP3953494B2 (ja) | アルキルスルホニルトリアゾール誘導体およびその製造方法 | |
JP2007137894A (ja) | トリアゾリノンの製造方法及び新規な中間体 | |
JP4028174B2 (ja) | トリアゾリンチオン誘導体の製造方法 | |
KR940009526B1 (ko) | 트리아졸리논의 제조방법 | |
JP3775691B2 (ja) | トリアゾリノンの製造方法及び新規な中間体 | |
JP3910652B2 (ja) | アルコキシトリアゾリノン類の製造方法 | |
JP3910653B2 (ja) | アルコキシトリアゾリノン類の製造方法 | |
JP3910655B2 (ja) | アルコキシトリアゾリノン類の製造方法 | |
JP4846092B2 (ja) | スルホニルアミノカルボニルトリアゾリノン類の塩の製造方法 | |
MXPA04011458A (es) | Procedimiento para la obtencion de 1, 2, 4-triazolilmetil-oxiranos. | |
JP2851919B2 (ja) | トリアゾロン誘導体の製造法および新規中間体 | |
JPH08259549A (ja) | 置換n−カルバモイル−テトラゾリノン類の製造方法 | |
US6472535B1 (en) | Oxidative hydrolysis of heteroaromatic thiones | |
JP3910654B2 (ja) | アルコキシトリアゾリノン類の製造方法 | |
JP4205180B2 (ja) | 1−アリール−4−カルバモイルテトラゾリノン類の製造方法 | |
JP2000506178A (ja) | 置換芳香族チオカルボン酸アミドの製造方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20060214 |
|
A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20060510 |
|
A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20060519 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20060814 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20070410 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20070424 |
|
R150 | Certificate of patent or registration of utility model |
Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
LAPS | Cancellation because of no payment of annual fees |