CA1072092A - 3-carbalkoxyamino-1h-2, 1,4-benzothiadiazine derivatives and process for their preparation - Google Patents
3-carbalkoxyamino-1h-2, 1,4-benzothiadiazine derivatives and process for their preparationInfo
- Publication number
- CA1072092A CA1072092A CA261,426A CA261426A CA1072092A CA 1072092 A CA1072092 A CA 1072092A CA 261426 A CA261426 A CA 261426A CA 1072092 A CA1072092 A CA 1072092A
- Authority
- CA
- Canada
- Prior art keywords
- nitro
- phenyl
- benzothiadiazine
- carbomethoxyamino
- thionocarbamoyl
- 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
Links
- 238000000034 method Methods 0.000 title claims abstract description 18
- 238000002360 preparation method Methods 0.000 title claims abstract description 11
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 15
- 239000000243 solution Substances 0.000 claims description 12
- 238000006243 chemical reaction Methods 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- 239000000126 substance Substances 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 claims description 4
- HVFXVOVOJMJPDT-UHFFFAOYSA-N [3-(methoxycarbonylamino)-1h-2,1,4-benzothiadiazin-7-yl] 3-(trifluoromethyl)benzenesulfonate Chemical compound C1=C2NSC(NC(=O)OC)=NC2=CC=C1OS(=O)(=O)C1=CC=CC(C(F)(F)F)=C1 HVFXVOVOJMJPDT-UHFFFAOYSA-N 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
- GRWZHXKQBITJKP-UHFFFAOYSA-L dithionite(2-) Chemical compound [O-]S(=O)S([O-])=O GRWZHXKQBITJKP-UHFFFAOYSA-L 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 2
- LJNJJEMEHCBZQQ-UHFFFAOYSA-N [3-(trifluoromethyl)phenyl] 4-chloro-3-nitrobenzenesulfonate Chemical compound C1=C(Cl)C([N+](=O)[O-])=CC(S(=O)(=O)OC=2C=C(C=CC=2)C(F)(F)F)=C1 LJNJJEMEHCBZQQ-UHFFFAOYSA-N 0.000 claims 1
- 229910052783 alkali metal Inorganic materials 0.000 claims 1
- 150000001340 alkali metals Chemical class 0.000 claims 1
- 239000012670 alkaline solution Substances 0.000 claims 1
- UCFFGYASXIPWPD-UHFFFAOYSA-N methyl hypochlorite Chemical compound COCl UCFFGYASXIPWPD-UHFFFAOYSA-N 0.000 claims 1
- 125000001209 o-nitrophenyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])[N+]([O-])=O 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 abstract description 7
- 244000000013 helminth Species 0.000 abstract description 2
- 238000004519 manufacturing process Methods 0.000 abstract description 2
- 241000242711 Fasciola hepatica Species 0.000 abstract 1
- 241000243788 Strongylida Species 0.000 abstract 1
- 208000006275 fascioliasis Diseases 0.000 abstract 1
- 230000002496 gastric effect Effects 0.000 abstract 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 24
- 239000002253 acid Substances 0.000 description 17
- -1 acyl radical Chemical class 0.000 description 15
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 9
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 8
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 8
- SEEPANYCNGTZFQ-UHFFFAOYSA-N sulfadiazine Chemical compound C1=CC(N)=CC=C1S(=O)(=O)NC1=NC=CC=N1 SEEPANYCNGTZFQ-UHFFFAOYSA-N 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- HAVZTGSQJIEKPI-UHFFFAOYSA-N benzothiadiazine Chemical compound C1=CC=C2C=NNSC2=C1 HAVZTGSQJIEKPI-UHFFFAOYSA-N 0.000 description 7
- NLXPDNKIQMAKCH-UHFFFAOYSA-N 1h-2,1,4-benzothiadiazine Chemical class C1=CC=C2NSC=NC2=C1 NLXPDNKIQMAKCH-UHFFFAOYSA-N 0.000 description 6
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- 238000002844 melting Methods 0.000 description 6
- 230000008018 melting Effects 0.000 description 6
- 239000007858 starting material Substances 0.000 description 6
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- 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 4
- DPJCXCZTLWNFOH-UHFFFAOYSA-N 2-nitroaniline Chemical class NC1=CC=CC=C1[N+]([O-])=O DPJCXCZTLWNFOH-UHFFFAOYSA-N 0.000 description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- 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 4
- 125000000449 nitro group Chemical class [O-][N+](*)=O 0.000 description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
- 241001630921 Chlorida Species 0.000 description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 229960000583 acetic acid Drugs 0.000 description 3
- 239000013543 active substance Substances 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Substances C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- 150000002431 hydrogen Chemical class 0.000 description 3
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- OGNVQLDIPUXYDH-ZPKKHLQPSA-N (2R,3R,4S)-3-(2-methylpropanoylamino)-4-(4-phenyltriazol-1-yl)-2-[(1R,2R)-1,2,3-trihydroxypropyl]-3,4-dihydro-2H-pyran-6-carboxylic acid Chemical compound CC(C)C(=O)N[C@H]1[C@H]([C@H](O)[C@H](O)CO)OC(C(O)=O)=C[C@@H]1N1N=NC(C=2C=CC=CC=2)=C1 OGNVQLDIPUXYDH-ZPKKHLQPSA-N 0.000 description 2
- FGUJEHLUNQOXRC-UHFFFAOYSA-N (4-amino-3-nitrophenyl) benzenesulfonate Chemical compound C1=C([N+]([O-])=O)C(N)=CC=C1OS(=O)(=O)C1=CC=CC=C1 FGUJEHLUNQOXRC-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 2
- 244000046052 Phaseolus vulgaris Species 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- PASDCCFISLVPSO-UHFFFAOYSA-N benzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 description 2
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 235000019439 ethyl acetate Nutrition 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000012442 inert solvent Substances 0.000 description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
- LEVJVKGPFAQPOI-UHFFFAOYSA-N phenylmethanone Chemical compound O=[C]C1=CC=CC=C1 LEVJVKGPFAQPOI-UHFFFAOYSA-N 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- XMVJITFPVVRMHC-UHFFFAOYSA-N roxarsone Chemical compound OC1=CC=C([As](O)(O)=O)C=C1[N+]([O-])=O XMVJITFPVVRMHC-UHFFFAOYSA-N 0.000 description 2
- 238000005245 sintering Methods 0.000 description 2
- 238000001665 trituration Methods 0.000 description 2
- SUVVFPGNNBUFED-UHFFFAOYSA-N (3-bromophenyl) 4-amino-3-nitrobenzenesulfonate Chemical compound C1=C([N+]([O-])=O)C(N)=CC=C1S(=O)(=O)OC1=CC=CC(Br)=C1 SUVVFPGNNBUFED-UHFFFAOYSA-N 0.000 description 1
- RLLUFVRELOURLR-UHFFFAOYSA-N (4-amino-3-nitrophenyl) 2-chlorobenzenesulfonate Chemical class C1=C([N+]([O-])=O)C(N)=CC=C1OS(=O)(=O)C1=CC=CC=C1Cl RLLUFVRELOURLR-UHFFFAOYSA-N 0.000 description 1
- BVJKOVDYRDCLHQ-UHFFFAOYSA-N (4-amino-3-nitrophenyl) 3-(trifluoromethyl)benzenesulfonate Chemical compound C1=C([N+]([O-])=O)C(N)=CC=C1OS(=O)(=O)C1=CC=CC(C(F)(F)F)=C1 BVJKOVDYRDCLHQ-UHFFFAOYSA-N 0.000 description 1
- LEJDKQFUIIHJPB-UHFFFAOYSA-N (4-amino-3-nitrophenyl) 4-butoxybenzenesulfonate Chemical class C1=CC(OCCCC)=CC=C1S(=O)(=O)OC1=CC=C(N)C([N+]([O-])=O)=C1 LEJDKQFUIIHJPB-UHFFFAOYSA-N 0.000 description 1
- FZEURURFKGYYQP-UHFFFAOYSA-N (4-amino-3-nitrophenyl) 4-chloro-3-methylbenzenesulfonate Chemical class C1=C(Cl)C(C)=CC(S(=O)(=O)OC=2C=C(C(N)=CC=2)[N+]([O-])=O)=C1 FZEURURFKGYYQP-UHFFFAOYSA-N 0.000 description 1
- MYJDQSVMFSRWKR-UHFFFAOYSA-N (4-amino-3-nitrophenyl) 5-chloro-2-methylbenzenesulfonate Chemical class CC1=CC=C(Cl)C=C1S(=O)(=O)OC1=CC=C(N)C([N+]([O-])=O)=C1 MYJDQSVMFSRWKR-UHFFFAOYSA-N 0.000 description 1
- QTBFCLOPCUGTCG-UHFFFAOYSA-N (4-methylphenyl) 4-amino-3-nitrobenzenesulfonate Chemical compound C1=CC(C)=CC=C1OS(=O)(=O)C1=CC=C(N)C([N+]([O-])=O)=C1 QTBFCLOPCUGTCG-UHFFFAOYSA-N 0.000 description 1
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 1
- UGRMITBWUVWUEB-UHFFFAOYSA-N 1-$l^{1}-oxidanyl-3-methylbenzene Chemical group CC1=CC=CC([O])=C1 UGRMITBWUVWUEB-UHFFFAOYSA-N 0.000 description 1
- RMSGQZDGSZOJMU-UHFFFAOYSA-N 1-butyl-2-phenylbenzene Chemical group CCCCC1=CC=CC=C1C1=CC=CC=C1 RMSGQZDGSZOJMU-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- IQXUIDYRTHQTET-UHFFFAOYSA-N 4-amino-3-nitrophenol Chemical compound NC1=CC=C(O)C=C1[N+]([O-])=O IQXUIDYRTHQTET-UHFFFAOYSA-N 0.000 description 1
- RPKWNMFDAOACCX-UHFFFAOYSA-N 4-chloro-3-nitrobenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=C(Cl)C([N+]([O-])=O)=C1 RPKWNMFDAOACCX-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
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- 101100087530 Caenorhabditis elegans rom-1 gene Proteins 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
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- 241000893172 Chabertia Species 0.000 description 1
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- 241001123946 Gaga Species 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- MUQNGPZZQDCDFT-JNQJZLCISA-N Halcinonide Chemical compound C1CC2=CC(=O)CC[C@]2(C)[C@]2(F)[C@@H]1[C@@H]1C[C@H]3OC(C)(C)O[C@@]3(C(=O)CCl)[C@@]1(C)C[C@@H]2O MUQNGPZZQDCDFT-JNQJZLCISA-N 0.000 description 1
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- 241000244174 Strongyloides Species 0.000 description 1
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- JZFICWYCTCCINF-UHFFFAOYSA-N Thiadiazin Chemical compound S=C1SC(C)NC(C)N1CCN1C(=S)SC(C)NC1C JZFICWYCTCCINF-UHFFFAOYSA-N 0.000 description 1
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- MWPQFRBSPKPQEU-UHFFFAOYSA-N [3-(methoxycarbonylamino)-1h-2,1,4-benzothiadiazin-7-yl] benzenesulfonate Chemical compound C1=C2NSC(NC(=O)OC)=NC2=CC=C1OS(=O)(=O)C1=CC=CC=C1 MWPQFRBSPKPQEU-UHFFFAOYSA-N 0.000 description 1
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- APVPOHHVBBYQAV-UHFFFAOYSA-N n-(4-aminophenyl)sulfonyloctadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NS(=O)(=O)C1=CC=C(N)C=C1 APVPOHHVBBYQAV-UHFFFAOYSA-N 0.000 description 1
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- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- DXNLDBASBALMSX-UHFFFAOYSA-N phenyl 4-chloro-3-nitrobenzenesulfonate Chemical compound C1=C(Cl)C([N+](=O)[O-])=CC(S(=O)(=O)OC=2C=CC=CC=2)=C1 DXNLDBASBALMSX-UHFFFAOYSA-N 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- RZWZRACFZGVKFM-UHFFFAOYSA-N propanoyl chloride Chemical compound CCC(Cl)=O RZWZRACFZGVKFM-UHFFFAOYSA-N 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
- DSNYFFJTZPIKFZ-UHFFFAOYSA-N propoxybenzene Chemical group CCCOC1=CC=CC=C1 DSNYFFJTZPIKFZ-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
- 239000011541 reaction mixture Substances 0.000 description 1
- 150000003385 sodium Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 229940086542 triethylamine Drugs 0.000 description 1
- ILWRPSCZWQJDMK-UHFFFAOYSA-N triethylazanium;chloride Chemical compound Cl.CCN(CC)CC ILWRPSCZWQJDMK-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
- C07D285/15—Six-membered rings
- C07D285/16—Thiadiazines; Hydrogenated thiadiazines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/10—Anthelmintics
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Tropical Medicine & Parasitology (AREA)
- General Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA328,985A CA1088953A (en) | 1975-09-19 | 1979-06-04 | O-nitrophenyl-thionocarbamoyl-carbabinates |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2541742A DE2541742C2 (de) | 1975-09-19 | 1975-09-19 | o-Nitro-phenyl-thionocarbamoyl-carbaminate und Verfahren zu ihrer Herstellung |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1072092A true CA1072092A (en) | 1980-02-19 |
Family
ID=5956858
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA261,426A Expired CA1072092A (en) | 1975-09-19 | 1976-09-17 | 3-carbalkoxyamino-1h-2, 1,4-benzothiadiazine derivatives and process for their preparation |
Country Status (30)
| Country | Link |
|---|---|
| US (1) | US4069325A (enExample) |
| JP (1) | JPS5253874A (enExample) |
| AT (1) | AT353279B (enExample) |
| AU (1) | AU505701B2 (enExample) |
| BE (1) | BE846379A (enExample) |
| CA (1) | CA1072092A (enExample) |
| CH (1) | CH624386A5 (enExample) |
| DE (1) | DE2541742C2 (enExample) |
| DK (1) | DK420576A (enExample) |
| ES (3) | ES451514A1 (enExample) |
| FI (1) | FI762652A7 (enExample) |
| FR (2) | FR2324307A1 (enExample) |
| GB (2) | GB1547841A (enExample) |
| GR (1) | GR60794B (enExample) |
| HU (1) | HU181444B (enExample) |
| IE (1) | IE43857B1 (enExample) |
| IL (1) | IL50504A (enExample) |
| IT (1) | IT1068301B (enExample) |
| KE (1) | KE3091A (enExample) |
| LU (1) | LU75815A1 (enExample) |
| MX (1) | MX3552E (enExample) |
| MY (1) | MY8100221A (enExample) |
| NL (1) | NL7610190A (enExample) |
| NO (1) | NO145161C (enExample) |
| NZ (1) | NZ182087A (enExample) |
| PH (1) | PH19955A (enExample) |
| PT (1) | PT65609A (enExample) |
| SE (2) | SE415478B (enExample) |
| ZA (1) | ZA765582B (enExample) |
| ZM (1) | ZM11976A1 (enExample) |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3655657A (en) * | 1970-02-24 | 1972-04-11 | Du Pont | 2 1 4-benzothiadiazine-3-carbamic acid esters |
| GB1340428A (en) * | 1971-04-13 | 1973-12-12 | Ici Ltd | Benzothiadiazine derivatives their preparation and veterinary and pharmaceutical compositions containing them |
| GB1350277A (en) * | 1971-09-22 | 1974-04-18 | Ici Ltd | Process for the manufacture of a benzimidazole derivative |
| CA1028337A (en) * | 1973-02-12 | 1978-03-21 | Syntex (U.S.A.) Llc | Carbalkoxythioureidobenzene derivatives having anthelmintic properties |
| DE2365362A1 (de) * | 1973-06-25 | 1975-01-23 | Hoechst Ag | 2,1,4-benzothiadiazinderivate und ihre herstellung |
-
1975
- 1975-09-19 DE DE2541742A patent/DE2541742C2/de not_active Expired
-
1976
- 1976-09-14 ES ES451514A patent/ES451514A1/es not_active Expired
- 1976-09-14 MX MX764924U patent/MX3552E/es unknown
- 1976-09-14 NL NL7610190A patent/NL7610190A/xx not_active Application Discontinuation
- 1976-09-16 CH CH1176276A patent/CH624386A5/de not_active IP Right Cessation
- 1976-09-16 FI FI762652A patent/FI762652A7/fi not_active Application Discontinuation
- 1976-09-16 LU LU75815A patent/LU75815A1/xx unknown
- 1976-09-16 SE SE7610309A patent/SE415478B/xx unknown
- 1976-09-16 HU HU76HO2152A patent/HU181444B/hu unknown
- 1976-09-17 GB GB38602/76A patent/GB1547841A/en not_active Expired
- 1976-09-17 GB GB19880/78A patent/GB1547842A/en not_active Expired
- 1976-09-17 CA CA261,426A patent/CA1072092A/en not_active Expired
- 1976-09-17 NO NO763195A patent/NO145161C/no unknown
- 1976-09-17 IL IL50504A patent/IL50504A/xx unknown
- 1976-09-17 US US05/724,246 patent/US4069325A/en not_active Expired - Lifetime
- 1976-09-17 AU AU17862/76A patent/AU505701B2/en not_active Ceased
- 1976-09-17 AT AT690576A patent/AT353279B/de active
- 1976-09-17 NZ NZ182087A patent/NZ182087A/xx unknown
- 1976-09-17 ZM ZM119/76A patent/ZM11976A1/xx unknown
- 1976-09-17 IE IE2061/76A patent/IE43857B1/en unknown
- 1976-09-17 IT IT27370/76A patent/IT1068301B/it active
- 1976-09-17 ZA ZA765582A patent/ZA765582B/xx unknown
- 1976-09-17 DK DK420576A patent/DK420576A/da not_active Application Discontinuation
- 1976-09-17 PT PT65609A patent/PT65609A/pt unknown
- 1976-09-18 GR GR51723A patent/GR60794B/el unknown
- 1976-09-18 JP JP51111325A patent/JPS5253874A/ja active Pending
- 1976-09-20 FR FR7628187A patent/FR2324307A1/fr active Granted
- 1976-09-20 BE BE170772A patent/BE846379A/xx not_active IP Right Cessation
-
1977
- 1977-10-01 ES ES462852A patent/ES462852A1/es not_active Expired
- 1977-10-01 ES ES462851A patent/ES462851A1/es not_active Expired
-
1978
- 1978-08-21 FR FR7824250A patent/FR2395992A1/fr active Granted
- 1978-12-11 PH PH21925A patent/PH19955A/en unknown
-
1979
- 1979-08-09 SE SE7906695A patent/SE7906695L/sv not_active Application Discontinuation
-
1980
- 1980-10-08 KE KE3091A patent/KE3091A/xx unknown
-
1981
- 1981-12-30 MY MY221/81A patent/MY8100221A/xx unknown
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MKEX | Expiry |