JPH0249281B2 - - Google Patents
Info
- Publication number
- JPH0249281B2 JPH0249281B2 JP55177972A JP17797280A JPH0249281B2 JP H0249281 B2 JPH0249281 B2 JP H0249281B2 JP 55177972 A JP55177972 A JP 55177972A JP 17797280 A JP17797280 A JP 17797280A JP H0249281 B2 JPH0249281 B2 JP H0249281B2
- Authority
- JP
- Japan
- Prior art keywords
- group
- carbon atoms
- nitro
- nitrothiophene
- methylsulfinyl
- 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 - Lifetime
Links
- 239000000203 mixture Substances 0.000 claims description 51
- 125000004432 carbon atom Chemical group C* 0.000 claims description 44
- -1 nitrothiophene compound Chemical class 0.000 claims description 22
- 125000000217 alkyl group Chemical group 0.000 claims description 18
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 14
- 239000002689 soil Substances 0.000 claims description 12
- 239000000126 substance Substances 0.000 claims description 11
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 10
- 239000004480 active ingredient Substances 0.000 claims description 8
- 230000000855 fungicidal effect Effects 0.000 claims description 8
- 229910052736 halogen Inorganic materials 0.000 claims description 7
- 239000007788 liquid Substances 0.000 claims description 7
- 125000003545 alkoxy group Chemical group 0.000 claims description 6
- 150000002367 halogens Chemical class 0.000 claims description 6
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 6
- HGXMBIPOHYXPHZ-UHFFFAOYSA-N 2-ethylsulfinyl-3-nitrothiophene Chemical group CCS(=O)C=1SC=CC=1[N+]([O-])=O HGXMBIPOHYXPHZ-UHFFFAOYSA-N 0.000 claims description 5
- 230000000844 anti-bacterial effect Effects 0.000 claims description 5
- 244000005700 microbiome Species 0.000 claims description 5
- QVKZITYQNWQZFP-UHFFFAOYSA-N 1-(5-methylsulfinyl-4-nitrothiophen-2-yl)ethanone Chemical group CC(=O)C1=CC([N+]([O-])=O)=C(S(C)=O)S1 QVKZITYQNWQZFP-UHFFFAOYSA-N 0.000 claims description 4
- VRDAZWVJTVQEMN-UHFFFAOYSA-N 2-ethylsulfanyl-3-nitrothiophene Chemical group CCSC=1SC=CC=1[N+]([O-])=O VRDAZWVJTVQEMN-UHFFFAOYSA-N 0.000 claims description 4
- DCXUYICICSONFO-UHFFFAOYSA-N 2-methylsulfinyl-3-nitrothiophene Chemical group CS(=O)C=1SC=CC=1[N+]([O-])=O DCXUYICICSONFO-UHFFFAOYSA-N 0.000 claims description 4
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 4
- 125000004076 pyridyl group Chemical group 0.000 claims description 4
- 239000007787 solid Substances 0.000 claims description 4
- PUEPJVYBCGPQAD-UHFFFAOYSA-N 4-methyl-2-methylsulfinyl-3-nitrothiophene Chemical group CC1=CSC(S(C)=O)=C1[N+]([O-])=O PUEPJVYBCGPQAD-UHFFFAOYSA-N 0.000 claims description 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 3
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 2
- 125000002252 acyl group Chemical group 0.000 claims description 2
- 125000005138 alkoxysulfonyl group Chemical group 0.000 claims description 2
- 125000003282 alkyl amino group Chemical group 0.000 claims description 2
- 125000003277 amino group Chemical group 0.000 claims description 2
- 125000004429 atom Chemical group 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
- 125000004472 dialkylaminosulfonyl group Chemical group 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 125000000858 thiocyanato group Chemical group *SC#N 0.000 claims description 2
- 238000002844 melting Methods 0.000 description 51
- 230000008018 melting Effects 0.000 description 51
- 150000001875 compounds Chemical class 0.000 description 32
- 239000000243 solution Substances 0.000 description 22
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 22
- 239000013543 active substance Substances 0.000 description 20
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 11
- 239000002904 solvent Substances 0.000 description 11
- ILVXOBCQQYKLDS-UHFFFAOYSA-N pyridine N-oxide Chemical compound [O-][N+]1=CC=CC=C1 ILVXOBCQQYKLDS-UHFFFAOYSA-N 0.000 description 9
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 description 9
- 241000196324 Embryophyta Species 0.000 description 8
- 239000000843 powder Substances 0.000 description 8
- 241000233866 Fungi Species 0.000 description 7
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 7
- 239000011541 reaction mixture Substances 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 241000233639 Pythium Species 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- HPZRMJLQGKQTSV-UHFFFAOYSA-N 2-(4-chlorophenyl)sulfinyl-3-nitrothiophene Chemical compound C1=CSC(S(=O)C=2C=CC(Cl)=CC=2)=C1[N+](=O)[O-] HPZRMJLQGKQTSV-UHFFFAOYSA-N 0.000 description 5
- 241000894006 Bacteria Species 0.000 description 5
- 241000813090 Rhizoctonia solani Species 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 239000002244 precipitate Substances 0.000 description 5
- 210000002268 wool Anatomy 0.000 description 5
- ZMPGYXOFMBZZSP-UHFFFAOYSA-N 2-methylsulfonyl-3-nitrothiophene Chemical compound CS(=O)(=O)C=1SC=CC=1[N+]([O-])=O ZMPGYXOFMBZZSP-UHFFFAOYSA-N 0.000 description 4
- JIZRGGUCOQKGQD-UHFFFAOYSA-N 2-nitrothiophene Chemical compound [O-][N+](=O)C1=CC=CS1 JIZRGGUCOQKGQD-UHFFFAOYSA-N 0.000 description 4
- WXGPXWASRVASAP-UHFFFAOYSA-N 4-methyl-2-methylsulfanyl-3-nitrothiophene Chemical compound CSC=1SC=C(C)C=1[N+]([O-])=O WXGPXWASRVASAP-UHFFFAOYSA-N 0.000 description 4
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 4
- 241000209140 Triticum Species 0.000 description 4
- 235000021307 Triticum Nutrition 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
- 239000012876 carrier material Substances 0.000 description 4
- 235000005822 corn Nutrition 0.000 description 4
- 239000002270 dispersing agent Substances 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000008187 granular material Substances 0.000 description 4
- 238000011534 incubation Methods 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000007800 oxidant agent Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- FKRVPKXXUZLDGS-UHFFFAOYSA-N 1-(5-methylsulfonyl-4-nitrothiophen-2-yl)ethanone Chemical compound CC(=O)C1=CC([N+]([O-])=O)=C(S(C)(=O)=O)S1 FKRVPKXXUZLDGS-UHFFFAOYSA-N 0.000 description 3
- HRSCIFAMHFPSPQ-UHFFFAOYSA-N 2,3-dimethyl-5-methylsulfinyl-4-nitrothiophene Chemical compound CC=1SC(S(C)=O)=C([N+]([O-])=O)C=1C HRSCIFAMHFPSPQ-UHFFFAOYSA-N 0.000 description 3
- VXMMSJFFDNYQHX-UHFFFAOYSA-N 2-(2-methylpropylsulfinyl)-3-nitrothiophene Chemical compound CC(C)CS(=O)C=1SC=CC=1[N+]([O-])=O VXMMSJFFDNYQHX-UHFFFAOYSA-N 0.000 description 3
- SAICZHBTHCJPKX-UHFFFAOYSA-N 2-(4-methoxyphenyl)sulfinyl-3-nitrothiophene Chemical compound C1=CC(OC)=CC=C1S(=O)C1=C([N+]([O-])=O)C=CS1 SAICZHBTHCJPKX-UHFFFAOYSA-N 0.000 description 3
- WHIDSBJYXKKPSQ-UHFFFAOYSA-N 2-(benzenesulfinyl)-3-nitrothiophene Chemical compound C1=CSC(S(=O)C=2C=CC=CC=2)=C1[N+](=O)[O-] WHIDSBJYXKKPSQ-UHFFFAOYSA-N 0.000 description 3
- ICBADHLYBBLMNV-UHFFFAOYSA-N 2-ethylsulfonyl-3-nitrothiophene Chemical compound CCS(=O)(=O)C=1SC=CC=1[N+]([O-])=O ICBADHLYBBLMNV-UHFFFAOYSA-N 0.000 description 3
- IAYMBJGNIYCBFY-UHFFFAOYSA-N 2-heptylsulfinyl-3-nitrothiophene Chemical compound CCCCCCCS(=O)C=1SC=CC=1[N+]([O-])=O IAYMBJGNIYCBFY-UHFFFAOYSA-N 0.000 description 3
- QKLJSJWLKQKOMK-UHFFFAOYSA-N 2-methylsulfinyl-3-nitro-4-phenylthiophene Chemical compound [O-][N+](=O)C1=C(S(=O)C)SC=C1C1=CC=CC=C1 QKLJSJWLKQKOMK-UHFFFAOYSA-N 0.000 description 3
- HHVICXVLYKMERV-UHFFFAOYSA-N 2-methylsulfonyl-3-nitro-4-phenylthiophene Chemical compound [O-][N+](=O)C1=C(S(=O)(=O)C)SC=C1C1=CC=CC=C1 HHVICXVLYKMERV-UHFFFAOYSA-N 0.000 description 3
- NHQDETIJWKXCTC-UHFFFAOYSA-N 3-chloroperbenzoic acid Chemical compound OOC(=O)C1=CC=CC(Cl)=C1 NHQDETIJWKXCTC-UHFFFAOYSA-N 0.000 description 3
- IJDBSVWSXSVOJN-UHFFFAOYSA-N 3-nitro-2-propylsulfinylthiophene Chemical compound CCCS(=O)C=1SC=CC=1[N+]([O-])=O IJDBSVWSXSVOJN-UHFFFAOYSA-N 0.000 description 3
- ZBCGQIVEGRPYTD-UHFFFAOYSA-N 4-chloro-2-methylsulfinyl-3-nitrothiophene Chemical compound CS(=O)C=1SC=C(Cl)C=1[N+]([O-])=O ZBCGQIVEGRPYTD-UHFFFAOYSA-N 0.000 description 3
- CLOMRYVUZNPCAF-UHFFFAOYSA-N 4-methyl-2-methylsulfonyl-3-nitrothiophene Chemical compound CC1=CSC(S(C)(=O)=O)=C1[N+]([O-])=O CLOMRYVUZNPCAF-UHFFFAOYSA-N 0.000 description 3
- FDWYZGPDSDPTDA-UHFFFAOYSA-N 5-(benzenesulfinyl)-4-nitrothiophene-2-carbonitrile Chemical compound C1=C(C#N)SC(S(=O)C=2C=CC=CC=2)=C1[N+](=O)[O-] FDWYZGPDSDPTDA-UHFFFAOYSA-N 0.000 description 3
- IJMNRYKXEOYIAO-UHFFFAOYSA-N 5-(benzenesulfonyl)-4-nitrothiophene-2-carbonitrile Chemical compound C1=C(C#N)SC(S(=O)(=O)C=2C=CC=CC=2)=C1[N+](=O)[O-] IJMNRYKXEOYIAO-UHFFFAOYSA-N 0.000 description 3
- HTQQONBHRDNVQP-UHFFFAOYSA-N 5-methylsulfinyl-4-nitrothiophene-2-carbonitrile Chemical compound CS(=O)C=1SC(C#N)=CC=1[N+]([O-])=O HTQQONBHRDNVQP-UHFFFAOYSA-N 0.000 description 3
- DCKDFDHRYFDQMV-UHFFFAOYSA-N 5-methylsulfonyl-4-nitrothiophene-2-carbonitrile Chemical compound CS(=O)(=O)C=1SC(C#N)=CC=1[N+]([O-])=O DCKDFDHRYFDQMV-UHFFFAOYSA-N 0.000 description 3
- 239000005995 Aluminium silicate Substances 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- 235000004431 Linum usitatissimum Nutrition 0.000 description 3
- 240000006240 Linum usitatissimum Species 0.000 description 3
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 3
- 241001459558 Monographella nivalis Species 0.000 description 3
- 241000233622 Phytophthora infestans Species 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 241000228454 Pyrenophora graminea Species 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 240000003768 Solanum lycopersicum Species 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 241000221576 Uromyces Species 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- 235000012211 aluminium silicate Nutrition 0.000 description 3
- 238000002485 combustion reaction Methods 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- 239000003995 emulsifying agent Substances 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- OPWXXVUHNAXZKI-UHFFFAOYSA-N ethyl 2-(3-nitrothiophen-2-yl)sulfinylacetate Chemical compound CCOC(=O)CS(=O)C=1SC=CC=1[N+]([O-])=O OPWXXVUHNAXZKI-UHFFFAOYSA-N 0.000 description 3
- CMOIYPIIEVISBK-UHFFFAOYSA-N ethyl 2-(3-nitrothiophen-2-yl)sulfonylacetate Chemical compound CCOC(=O)CS(=O)(=O)C=1SC=CC=1[N+]([O-])=O CMOIYPIIEVISBK-UHFFFAOYSA-N 0.000 description 3
- MHPUJBYOTWIXDJ-UHFFFAOYSA-N ethyl 5-methylsulfinyl-4-nitrothiophene-2-carboxylate Chemical compound CCOC(=O)C1=CC([N+]([O-])=O)=C(S(C)=O)S1 MHPUJBYOTWIXDJ-UHFFFAOYSA-N 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 239000001963 growth medium Substances 0.000 description 3
- 239000010903 husk Substances 0.000 description 3
- 208000015181 infectious disease Diseases 0.000 description 3
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- 239000000080 wetting agent Substances 0.000 description 3
- PGUSMFUVOAVTBI-UHFFFAOYSA-N (5-methylsulfinyl-4-nitrothiophen-2-yl)methanol Chemical compound CS(=O)C=1SC(CO)=CC=1[N+]([O-])=O PGUSMFUVOAVTBI-UHFFFAOYSA-N 0.000 description 2
- FYYRMXFEHFMOGK-UHFFFAOYSA-N (5-methylsulfonyl-4-nitrothiophen-2-yl)methanol Chemical compound CS(=O)(=O)C=1SC(CO)=CC=1[N+]([O-])=O FYYRMXFEHFMOGK-UHFFFAOYSA-N 0.000 description 2
- QJRUYGWLTKUOBH-UHFFFAOYSA-N 1-(5-ethylsulfinyl-4-nitrothiophen-2-yl)ethanone Chemical compound CCS(=O)C=1SC(C(C)=O)=CC=1[N+]([O-])=O QJRUYGWLTKUOBH-UHFFFAOYSA-N 0.000 description 2
- BWJWOBDPVFTAHK-UHFFFAOYSA-N 1-(5-ethylsulfonyl-4-nitrothiophen-2-yl)ethanone Chemical compound CCS(=O)(=O)C=1SC(C(C)=O)=CC=1[N+]([O-])=O BWJWOBDPVFTAHK-UHFFFAOYSA-N 0.000 description 2
- NAVUGOOAMDYPGW-UHFFFAOYSA-N 1-(5-methylsulfinyl-4-nitrothiophen-2-yl)ethanol Chemical compound CC(O)C1=CC([N+]([O-])=O)=C(S(C)=O)S1 NAVUGOOAMDYPGW-UHFFFAOYSA-N 0.000 description 2
- CVRISYOTUDUYQF-UHFFFAOYSA-N 1-(5-methylsulfonyl-4-nitrothiophen-2-yl)ethanol Chemical compound CC(O)C1=CC([N+]([O-])=O)=C(S(C)(=O)=O)S1 CVRISYOTUDUYQF-UHFFFAOYSA-N 0.000 description 2
- SCVJRXQHFJXZFZ-KVQBGUIXSA-N 2-amino-9-[(2r,4s,5r)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-3h-purine-6-thione Chemical class C1=2NC(N)=NC(=S)C=2N=CN1[C@H]1C[C@H](O)[C@@H](CO)O1 SCVJRXQHFJXZFZ-KVQBGUIXSA-N 0.000 description 2
- YQEZCALGFMNYSM-UHFFFAOYSA-N 4-methyl-2-methylsulfinyl-5-nitro-1,3-thiazole Chemical compound CC=1N=C(S(C)=O)SC=1[N+]([O-])=O YQEZCALGFMNYSM-UHFFFAOYSA-N 0.000 description 2
- ZJAFQAPHWPSKRZ-UHFFFAOYSA-N 4-nitrobenzenecarboperoxoic acid Chemical compound OOC(=O)C1=CC=C([N+]([O-])=O)C=C1 ZJAFQAPHWPSKRZ-UHFFFAOYSA-N 0.000 description 2
- UHPMCKVQTMMPCG-UHFFFAOYSA-N 5,8-dihydroxy-2-methoxy-6-methyl-7-(2-oxopropyl)naphthalene-1,4-dione Chemical compound CC1=C(CC(C)=O)C(O)=C2C(=O)C(OC)=CC(=O)C2=C1O UHPMCKVQTMMPCG-UHFFFAOYSA-N 0.000 description 2
- TZXPXVXSJKKQPR-UHFFFAOYSA-N 5-(bromomethyl)-2-methylsulfinyl-3-nitrothiophene Chemical compound CS(=O)C=1SC(CBr)=CC=1[N+]([O-])=O TZXPXVXSJKKQPR-UHFFFAOYSA-N 0.000 description 2
- FAWPEKCTMTXVAT-UHFFFAOYSA-N 5-methylsulfanyl-4-nitrothiophene-2-carbaldehyde Chemical compound CSC=1SC(C=O)=CC=1[N+]([O-])=O FAWPEKCTMTXVAT-UHFFFAOYSA-N 0.000 description 2
- TUOYCTQDKBMTKM-UHFFFAOYSA-N 5-methylsulfanyl-4-nitrothiophene-2-carbonitrile Chemical compound CSC=1SC(C#N)=CC=1[N+]([O-])=O TUOYCTQDKBMTKM-UHFFFAOYSA-N 0.000 description 2
- 229920001817 Agar Polymers 0.000 description 2
- 244000075850 Avena orientalis Species 0.000 description 2
- 235000007319 Avena orientalis Nutrition 0.000 description 2
- MBSQGFVGNUIDKK-UHFFFAOYSA-N C[S+](C1=C2OCCO1)C(S(C)(=O)=O)=C2[N+]([O-])=O Chemical compound C[S+](C1=C2OCCO1)C(S(C)(=O)=O)=C2[N+]([O-])=O MBSQGFVGNUIDKK-UHFFFAOYSA-N 0.000 description 2
- GHJNYAGXICOIGK-UHFFFAOYSA-N C[S+](C1=C2OCCO1)C(S(C)=O)=C2[N+]([O-])=O Chemical compound C[S+](C1=C2OCCO1)C(S(C)=O)=C2[N+]([O-])=O GHJNYAGXICOIGK-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- 241000223218 Fusarium Species 0.000 description 2
- 229920001732 Lignosulfonate Polymers 0.000 description 2
- GQPLMRYTRLFLPF-UHFFFAOYSA-N Nitrous Oxide Chemical compound [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 description 2
- PKUWKAXTAVNIJR-UHFFFAOYSA-N O,O-diethyl hydrogen thiophosphate Chemical compound CCOP(O)(=S)OCC PKUWKAXTAVNIJR-UHFFFAOYSA-N 0.000 description 2
- KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 description 2
- 244000046052 Phaseolus vulgaris Species 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 230000000895 acaricidal effect Effects 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000000443 aerosol Substances 0.000 description 2
- 239000008272 agar Substances 0.000 description 2
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 2
- 239000000440 bentonite Substances 0.000 description 2
- 229910000278 bentonite Inorganic materials 0.000 description 2
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 235000013339 cereals Nutrition 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 150000002191 fatty alcohols Chemical class 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000002917 insecticide Substances 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 235000010755 mineral Nutrition 0.000 description 2
- MWUXSHHQAYIFBG-UHFFFAOYSA-N nitrogen oxide Inorganic materials O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 230000001717 pathogenic effect Effects 0.000 description 2
- 239000000575 pesticide Substances 0.000 description 2
- 238000001953 recrystallisation Methods 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 230000001988 toxicity Effects 0.000 description 2
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- NHOWDZOIZKMVAI-UHFFFAOYSA-N (2-chlorophenyl)(4-chlorophenyl)pyrimidin-5-ylmethanol Chemical compound C=1N=CN=CC=1C(C=1C(=CC=CC=1)Cl)(O)C1=CC=C(Cl)C=C1 NHOWDZOIZKMVAI-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur 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
- C07D333/42—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur 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 with nitro or nitroso radicals directly attached to ring carbon atoms
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
- A01N43/10—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings with sulfur as the ring hetero atom
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen 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
- C07D213/62—Oxygen or sulfur atoms
- C07D213/70—Sulfur atoms
- C07D213/71—Sulfur atoms to which a second hetero atom is attached
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL7909124 | 1979-12-19 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5697282A JPS5697282A (en) | 1981-08-05 |
| JPH0249281B2 true JPH0249281B2 (US07943777-20110517-C00090.png) | 1990-10-29 |
Family
ID=19834337
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP17797280A Granted JPS5697282A (en) | 1979-12-19 | 1980-12-16 | Nitrothiophene compound* its manufacture and its composition |
Country Status (23)
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE4643T1 (de) * | 1979-12-19 | 1983-09-15 | Duphar International Research B.V | Nitrothiophene, verfahren zur herstellung der verbindungen sowie fungizide und/oder bakterizide zusammensetzungen auf der basis dieser verbindungen. |
| DE3763409D1 (de) * | 1986-02-19 | 1990-08-02 | Duphar Int Res | Thio-verbindungen und ihre wirkung als fungizide. |
| EP0273602A1 (en) * | 1986-12-05 | 1988-07-06 | Eli Lilly And Company | 3-Cyano-4-arylthiophenes |
| DE3812177A1 (de) * | 1988-04-13 | 1989-10-26 | Bayer Ag | 2-phenylsulfinyl-nitro-pyridine, verfahren zu ihrer herstellung und ihre verwendung |
| TW319681B (US07943777-20110517-C00090.png) * | 1995-09-01 | 1997-11-11 | Rohm & Haas | |
| DE19540951A1 (de) * | 1995-11-03 | 1997-05-07 | Basf Ag | Wasserabsorbierende, schaumförmige, vernetzte Polymerisate, Verfahren zu ihrer Herstellung und ihre Verwendung |
| DE19607529A1 (de) | 1996-02-28 | 1997-09-04 | Basf Ag | Absorberelement aus superabsorbierenden Schäumen mit anisotropem Quellverhalten |
| DE19809540A1 (de) | 1998-03-05 | 1999-09-09 | Basf Ag | Wasserabsorbierende, schaumförmige, vernetzte Polymerisate, Verfahren zu ihrer Herstellung und ihre Verwendung |
| US7220821B2 (en) * | 2002-02-04 | 2007-05-22 | Basf Aktiengesellschaft | Process for the reduction of the residual monomer content of water-absorbent foam |
| US8680139B2 (en) | 2009-04-01 | 2014-03-25 | Progenra | Anti-neoplastic compounds, compositions and methods |
| GB201514021D0 (en) | 2015-08-07 | 2015-09-23 | Arner Elias Set Jeno | Novel Pyridines and their use in the treatment of cancer |
| AU2018218522B2 (en) | 2017-02-07 | 2021-08-05 | Oblique Therapeutics Ab | Hydrocarbylsulfonyl-substituted pyridines and their use in the treatment of cancer |
| CN110382465A (zh) | 2017-02-07 | 2019-10-25 | 欧比力克治疗公司 | 亚磺酰基吡啶和其在癌症治疗中的用途 |
| WO2018146471A1 (en) * | 2017-02-07 | 2018-08-16 | Oblique Therapeutics Ab | Heterocyclylsulfonyl-substituted pyridines and their use in the treatment of cancer |
| AU2018218519B2 (en) * | 2017-02-07 | 2021-08-05 | Oblique Therapeutics Ab | Heteroarylsulfonyl-substituted pyridines and their use in the treatment of cancer |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3682968A (en) * | 1969-06-25 | 1972-08-08 | Merck & Co Inc | Anti-inflammatory salicylic acid derivatives |
| JPS494471A (US07943777-20110517-C00090.png) * | 1972-04-24 | 1974-01-16 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2389128A (en) * | 1941-12-13 | 1945-11-20 | Parke Davis & Co | Sulphones and method of preparing same |
| US2562988A (en) * | 1948-12-18 | 1951-08-07 | Texas Co | Nitro-and thiocyano-substituted thiophene compounds |
| ATE4643T1 (de) * | 1979-12-19 | 1983-09-15 | Duphar International Research B.V | Nitrothiophene, verfahren zur herstellung der verbindungen sowie fungizide und/oder bakterizide zusammensetzungen auf der basis dieser verbindungen. |
-
1980
- 1980-11-26 AT AT80201119T patent/ATE4643T1/de not_active IP Right Cessation
- 1980-11-26 DE DE8080201119T patent/DE3064846D1/de not_active Expired
- 1980-11-26 EP EP80201119A patent/EP0031173B1/en not_active Expired
- 1980-12-16 IL IL61729A patent/IL61729A/xx unknown
- 1980-12-16 JP JP17797280A patent/JPS5697282A/ja active Granted
- 1980-12-16 YU YU03171/80A patent/YU317180A/xx unknown
- 1980-12-16 DD DD80226152A patent/DD155384A5/de unknown
- 1980-12-16 AU AU65430/80A patent/AU536144B2/en not_active Ceased
- 1980-12-16 NZ NZ195851A patent/NZ195851A/xx unknown
- 1980-12-16 AR AR283650A patent/AR227657A1/es active
- 1980-12-16 BG BG8050009A patent/BG34756A3/xx unknown
- 1980-12-16 PL PL1980228509A patent/PL125938B1/pl unknown
- 1980-12-16 HU HU803015A patent/HU188758B/hu not_active IP Right Cessation
- 1980-12-16 CA CA000366900A patent/CA1150264A/en not_active Expired
- 1980-12-16 BR BR8008235A patent/BR8008235A/pt unknown
- 1980-12-16 EG EG774/80A patent/EG14491A/xx active
- 1980-12-16 DK DK534780A patent/DK157299C/da not_active IP Right Cessation
- 1980-12-17 ZA ZA00807898A patent/ZA807898B/xx unknown
- 1980-12-17 CS CS808935A patent/CS221944B2/cs unknown
- 1980-12-17 ES ES497831A patent/ES8200676A1/es not_active Expired
- 1980-12-18 RO RO102884A patent/RO80925B/ro unknown
-
1981
- 1981-05-04 SU SU813276203A patent/SU1050564A3/ru active
-
1982
- 1982-03-25 US US06/361,758 patent/US4451660A/en not_active Expired - Fee Related
-
1983
- 1983-10-20 US US06/543,895 patent/US4649154A/en not_active Expired - Fee Related
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3682968A (en) * | 1969-06-25 | 1972-08-08 | Merck & Co Inc | Anti-inflammatory salicylic acid derivatives |
| JPS494471A (US07943777-20110517-C00090.png) * | 1972-04-24 | 1974-01-16 |
Also Published As
| Publication number | Publication date |
|---|---|
| YU317180A (en) | 1983-02-28 |
| BR8008235A (pt) | 1981-07-07 |
| IL61729A0 (en) | 1981-01-30 |
| ATE4643T1 (de) | 1983-09-15 |
| EG14491A (en) | 1984-06-30 |
| NZ195851A (en) | 1983-09-30 |
| AR227657A1 (es) | 1982-11-30 |
| US4649154A (en) | 1987-03-10 |
| IL61729A (en) | 1986-08-31 |
| ES497831A0 (es) | 1981-11-01 |
| DE3064846D1 (en) | 1983-10-20 |
| SU1050564A3 (ru) | 1983-10-23 |
| CS221944B2 (en) | 1983-04-29 |
| CA1150264A (en) | 1983-07-19 |
| RO80925A (ro) | 1983-04-29 |
| EP0031173B1 (en) | 1983-09-14 |
| HU188758B (en) | 1986-05-28 |
| ES8200676A1 (es) | 1981-11-01 |
| EP0031173A1 (en) | 1981-07-01 |
| DK157299C (da) | 1990-05-07 |
| DK157299B (da) | 1989-12-04 |
| ZA807898B (en) | 1982-07-28 |
| AU6543080A (en) | 1981-06-25 |
| US4451660A (en) | 1984-05-29 |
| BG34756A3 (en) | 1983-11-15 |
| RO80925B (ro) | 1983-04-30 |
| DK534780A (da) | 1981-06-20 |
| DD155384A5 (de) | 1982-06-09 |
| AU536144B2 (en) | 1984-04-19 |
| JPS5697282A (en) | 1981-08-05 |
| PL228509A1 (US07943777-20110517-C00090.png) | 1982-02-01 |
| PL125938B1 (en) | 1983-06-30 |
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