NO140592B - Analogifremgangsmaate til fremstilling av antelmintisk virksomme 2-karbalkoksyamino-benzimidazolyl-5-(6)-sulfonsyre-fenylestere - Google Patents
Analogifremgangsmaate til fremstilling av antelmintisk virksomme 2-karbalkoksyamino-benzimidazolyl-5-(6)-sulfonsyre-fenylestere Download PDFInfo
- Publication number
- NO140592B NO140592B NO752945A NO752945A NO140592B NO 140592 B NO140592 B NO 140592B NO 752945 A NO752945 A NO 752945A NO 752945 A NO752945 A NO 752945A NO 140592 B NO140592 B NO 140592B
- Authority
- NO
- Norway
- Prior art keywords
- phenyl ester
- formula
- acid
- benzenesulfonic acid
- ester
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 12
- 230000000694 effects Effects 0.000 title description 3
- 238000002360 preparation method Methods 0.000 title description 3
- -1 cyanamide carboxylate Chemical class 0.000 claims description 23
- 150000004987 o-phenylenediamines Chemical class 0.000 claims description 11
- 125000004432 carbon atom Chemical group C* 0.000 claims description 10
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- YHMFTWZCHPQXRM-UHFFFAOYSA-N dichloromethylidenecarbamic acid Chemical compound OC(=O)N=C(Cl)Cl YHMFTWZCHPQXRM-UHFFFAOYSA-N 0.000 claims description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 3
- 125000005843 halogen group Chemical group 0.000 claims description 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 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 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
- 238000002844 melting Methods 0.000 description 41
- 230000008018 melting Effects 0.000 description 41
- 238000000354 decomposition reaction Methods 0.000 description 23
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 18
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 18
- 239000003921 oil Substances 0.000 description 16
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 15
- 238000006243 chemical reaction Methods 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 12
- 238000003776 cleavage reaction Methods 0.000 description 10
- ROVPGRDMDASARO-UHFFFAOYSA-N phenyl 3,4-diaminobenzenesulfonate Chemical compound C1=C(N)C(N)=CC=C1S(=O)(=O)OC1=CC=CC=C1 ROVPGRDMDASARO-UHFFFAOYSA-N 0.000 description 10
- 230000007017 scission Effects 0.000 description 10
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 9
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 8
- 239000000203 mixture Substances 0.000 description 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
- NEZIKMJTIOLUGU-UHFFFAOYSA-N phenyl 4-amino-3-nitrobenzenesulfonate Chemical compound C1=C([N+]([O-])=O)C(N)=CC=C1S(=O)(=O)OC1=CC=CC=C1 NEZIKMJTIOLUGU-UHFFFAOYSA-N 0.000 description 6
- 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 6
- 235000011121 sodium hydroxide Nutrition 0.000 description 6
- NAWXUBYGYWOOIX-SFHVURJKSA-N (2s)-2-[[4-[2-(2,4-diaminoquinazolin-6-yl)ethyl]benzoyl]amino]-4-methylidenepentanedioic acid Chemical compound C1=CC2=NC(N)=NC(N)=C2C=C1CCC1=CC=C(C(=O)N[C@@H](CC(=C)C(O)=O)C(O)=O)C=C1 NAWXUBYGYWOOIX-SFHVURJKSA-N 0.000 description 5
- 229960000583 acetic acid Drugs 0.000 description 5
- 239000002585 base Substances 0.000 description 5
- 239000011541 reaction mixture Substances 0.000 description 5
- 239000007858 starting material Substances 0.000 description 5
- CGWGGQHTSYXUDD-UHFFFAOYSA-N (3-bromophenyl) 3,4-diaminobenzenesulfonate Chemical compound C1=C(N)C(N)=CC=C1S(=O)(=O)OC1=CC=CC(Br)=C1 CGWGGQHTSYXUDD-UHFFFAOYSA-N 0.000 description 4
- BTQROPWNFKTNSO-UHFFFAOYSA-N (3-bromophenyl) 4-chloro-3-nitrobenzenesulfonate Chemical compound C1=C(Cl)C([N+](=O)[O-])=CC(S(=O)(=O)OC=2C=C(Br)C=CC=2)=C1 BTQROPWNFKTNSO-UHFFFAOYSA-N 0.000 description 4
- ZKHUTBZCEQOSDR-UHFFFAOYSA-N (3-chlorophenyl) 3,4-diaminobenzenesulfonate Chemical compound C1=C(N)C(N)=CC=C1S(=O)(=O)OC1=CC=CC(Cl)=C1 ZKHUTBZCEQOSDR-UHFFFAOYSA-N 0.000 description 4
- MVWMIZKBHIIUJW-UHFFFAOYSA-N (3-chlorophenyl) 4-amino-3-nitrobenzenesulfonate Chemical compound C1=C([N+]([O-])=O)C(N)=CC=C1S(=O)(=O)OC1=CC=CC(Cl)=C1 MVWMIZKBHIIUJW-UHFFFAOYSA-N 0.000 description 4
- BVDJGIMOJFTONF-UHFFFAOYSA-N (3-ethoxyphenyl) 3,4-diaminobenzenesulfonate Chemical compound CCOC1=CC=CC(OS(=O)(=O)C=2C=C(N)C(N)=CC=2)=C1 BVDJGIMOJFTONF-UHFFFAOYSA-N 0.000 description 4
- KRCUXSWQRHFAKL-UHFFFAOYSA-N (3-ethoxyphenyl) 4-amino-3-nitrobenzenesulfonate Chemical compound CCOC1=CC=CC(OS(=O)(=O)C=2C=C(C(N)=CC=2)[N+]([O-])=O)=C1 KRCUXSWQRHFAKL-UHFFFAOYSA-N 0.000 description 4
- GUSLKHUEMKHWEG-UHFFFAOYSA-N (3-methoxyphenyl) 4-amino-3-nitrobenzenesulfonate Chemical compound COC1=CC=CC(OS(=O)(=O)C=2C=C(C(N)=CC=2)[N+]([O-])=O)=C1 GUSLKHUEMKHWEG-UHFFFAOYSA-N 0.000 description 4
- AZRXKRNSQPFLGD-UHFFFAOYSA-N (3-methoxyphenyl) 4-chloro-3-nitrobenzenesulfonate Chemical compound COC1=CC=CC(OS(=O)(=O)C=2C=C(C(Cl)=CC=2)[N+]([O-])=O)=C1 AZRXKRNSQPFLGD-UHFFFAOYSA-N 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- 241001465754 Metazoa Species 0.000 description 4
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
- PEOUQUKUHBWKGO-UHFFFAOYSA-N [3-(trifluoromethyl)phenyl] 4-amino-3-nitrobenzenesulfonate Chemical compound C1=C([N+]([O-])=O)C(N)=CC=C1S(=O)(=O)OC1=CC=CC(C(F)(F)F)=C1 PEOUQUKUHBWKGO-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 239000003610 charcoal Substances 0.000 description 4
- XMJHPCRAQCTCFT-UHFFFAOYSA-N methyl chloroformate Chemical compound COC(Cl)=O XMJHPCRAQCTCFT-UHFFFAOYSA-N 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- NXOKKXACBQESEI-UHFFFAOYSA-N (3-bromophenyl) 2-(methoxycarbonylamino)-3h-benzimidazole-5-sulfonate Chemical compound C1=C2NC(NC(=O)OC)=NC2=CC=C1S(=O)(=O)OC1=CC=CC(Br)=C1 NXOKKXACBQESEI-UHFFFAOYSA-N 0.000 description 3
- 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 3
- XPLMXXAWBCYERB-UHFFFAOYSA-N (3-chlorophenyl) 2-(methoxycarbonylamino)-3h-benzimidazole-5-sulfonate Chemical compound C1=C2NC(NC(=O)OC)=NC2=CC=C1S(=O)(=O)OC1=CC=CC(Cl)=C1 XPLMXXAWBCYERB-UHFFFAOYSA-N 0.000 description 3
- NPPCVICNVNTDDO-UHFFFAOYSA-N (3-chlorophenyl) 4-chloro-3-nitrobenzenesulfonate Chemical compound C1=C(Cl)C([N+](=O)[O-])=CC(S(=O)(=O)OC=2C=C(Cl)C=CC=2)=C1 NPPCVICNVNTDDO-UHFFFAOYSA-N 0.000 description 3
- KKQNCKWAALXEKI-UHFFFAOYSA-N (3-methoxyphenyl) 3,4-diaminobenzenesulfonate Chemical compound COC1=CC=CC(OS(=O)(=O)C=2C=C(N)C(N)=CC=2)=C1 KKQNCKWAALXEKI-UHFFFAOYSA-N 0.000 description 3
- XFMINSQCONUQCO-UHFFFAOYSA-N (3-methylphenyl) 3,4-diaminobenzenesulfonate Chemical compound CC1=CC=CC(OS(=O)(=O)C=2C=C(N)C(N)=CC=2)=C1 XFMINSQCONUQCO-UHFFFAOYSA-N 0.000 description 3
- AGSDJTRUYDYOKC-UHFFFAOYSA-N (3-methylphenyl) 4-chloro-3-nitrobenzenesulfonate Chemical compound CC1=CC=CC(OS(=O)(=O)C=2C=C(C(Cl)=CC=2)[N+]([O-])=O)=C1 AGSDJTRUYDYOKC-UHFFFAOYSA-N 0.000 description 3
- SEWNAJIUKSTYOP-UHFFFAOYSA-N 4-chloro-3-nitrobenzenesulfonyl chloride Chemical compound [O-][N+](=O)C1=CC(S(Cl)(=O)=O)=CC=C1Cl SEWNAJIUKSTYOP-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- OZJCFJYLCGBGFM-UHFFFAOYSA-N [3-(trifluoromethyl)phenyl] 3,4-diaminobenzenesulfonate Chemical compound C1=C(N)C(N)=CC=C1S(=O)(=O)OC1=CC=CC(C(F)(F)F)=C1 OZJCFJYLCGBGFM-UHFFFAOYSA-N 0.000 description 3
- 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 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 239000012043 crude product Substances 0.000 description 3
- 235000013601 eggs Nutrition 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 239000012362 glacial acetic acid Substances 0.000 description 3
- 150000007524 organic acids Chemical class 0.000 description 3
- JMVOTQMMWZCLEX-UHFFFAOYSA-N phenyl 2-(methoxycarbonylamino)-3h-benzimidazole-5-sulfonate Chemical compound C1=C2NC(NC(=O)OC)=NC2=CC=C1S(=O)(=O)OC1=CC=CC=C1 JMVOTQMMWZCLEX-UHFFFAOYSA-N 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 238000000746 purification Methods 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
- UMRIXOOKYJPSSR-UHFFFAOYSA-N (3-ethoxyphenyl) 2-(methoxycarbonylamino)-3h-benzimidazole-5-sulfonate Chemical compound CCOC1=CC=CC(OS(=O)(=O)C=2C=C3NC(NC(=O)OC)=NC3=CC=2)=C1 UMRIXOOKYJPSSR-UHFFFAOYSA-N 0.000 description 2
- QCCQKSLEMRUDGL-UHFFFAOYSA-N (3-methylphenyl) 2-(methoxycarbonylamino)-3h-benzimidazole-5-sulfonate Chemical compound C1=C2NC(NC(=O)OC)=NC2=CC=C1S(=O)(=O)OC1=CC=CC(C)=C1 QCCQKSLEMRUDGL-UHFFFAOYSA-N 0.000 description 2
- HMEHAKJPTXFDAV-UHFFFAOYSA-N (3-methylphenyl) 4-amino-3-nitrobenzenesulfonate Chemical compound CC1=CC=CC(OS(=O)(=O)C=2C=C(C(N)=CC=2)[N+]([O-])=O)=C1 HMEHAKJPTXFDAV-UHFFFAOYSA-N 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 241001494479 Pecora Species 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 239000007868 Raney catalyst Substances 0.000 description 2
- NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 description 2
- 229910000564 Raney nickel Inorganic materials 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- VZKYXBAJKUNMKC-UHFFFAOYSA-N [3-(trifluoromethyl)phenyl] 2-(methoxycarbonylamino)-3h-benzimidazole-5-sulfonate Chemical compound C1=C2NC(NC(=O)OC)=NC2=CC=C1S(=O)(=O)OC1=CC=CC(C(F)(F)F)=C1 VZKYXBAJKUNMKC-UHFFFAOYSA-N 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 229910021529 ammonia Inorganic materials 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
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- AOGYCOYQMAVAFD-UHFFFAOYSA-N chlorocarbonic acid Chemical class OC(Cl)=O AOGYCOYQMAVAFD-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000010696 ester oil Substances 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N formic acid Substances OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 244000000013 helminth Species 0.000 description 2
- 239000012442 inert solvent Substances 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- NNBBQNFHCVVQHZ-UHFFFAOYSA-N methyl carbamimidothioate;sulfuric acid Chemical compound CSC(N)=N.OS(O)(=O)=O NNBBQNFHCVVQHZ-UHFFFAOYSA-N 0.000 description 2
- IUROBCDXAGBTOV-UHFFFAOYSA-N methyl n-(dichloromethylidene)carbamate Chemical compound COC(=O)N=C(Cl)Cl IUROBCDXAGBTOV-UHFFFAOYSA-N 0.000 description 2
- LCBJJCQPMXGINF-UHFFFAOYSA-N methyl n-[bis(methylsulfanyl)methylidene]carbamate Chemical compound COC(=O)N=C(SC)SC LCBJJCQPMXGINF-UHFFFAOYSA-N 0.000 description 2
- 150000007530 organic bases Chemical group 0.000 description 2
- 244000045947 parasite Species 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 238000001953 recrystallisation Methods 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 2
- 235000017557 sodium bicarbonate Nutrition 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- BYGWCYMTSFEQLM-UHFFFAOYSA-N (3,5-dichlorophenyl) 2-(methoxycarbonylamino)-3h-benzimidazole-5-sulfonate Chemical compound C1=C2NC(NC(=O)OC)=NC2=CC=C1S(=O)(=O)OC1=CC(Cl)=CC(Cl)=C1 BYGWCYMTSFEQLM-UHFFFAOYSA-N 0.000 description 1
- BGKBIDOMOFMKSU-UHFFFAOYSA-N (3,5-dichlorophenyl) 3,4-diaminobenzenesulfonate Chemical compound C1=C(N)C(N)=CC=C1S(=O)(=O)OC1=CC(Cl)=CC(Cl)=C1 BGKBIDOMOFMKSU-UHFFFAOYSA-N 0.000 description 1
- WOWQQLGSWXREKK-UHFFFAOYSA-N (3,5-dichlorophenyl) 4-amino-3-nitrobenzenesulfonate Chemical compound C1=C([N+]([O-])=O)C(N)=CC=C1S(=O)(=O)OC1=CC(Cl)=CC(Cl)=C1 WOWQQLGSWXREKK-UHFFFAOYSA-N 0.000 description 1
- BMKAZDKKRQRUDH-UHFFFAOYSA-N (3,5-dichlorophenyl) 4-chloro-3-nitrobenzenesulfonate Chemical compound C1=C(Cl)C([N+](=O)[O-])=CC(S(=O)(=O)OC=2C=C(Cl)C=C(Cl)C=2)=C1 BMKAZDKKRQRUDH-UHFFFAOYSA-N 0.000 description 1
- REDRJDQKXRSTBY-UHFFFAOYSA-N (3-cyanophenyl) 4-amino-3-nitrobenzenesulfonate Chemical compound C1=C([N+]([O-])=O)C(N)=CC=C1S(=O)(=O)OC1=CC=CC(C#N)=C1 REDRJDQKXRSTBY-UHFFFAOYSA-N 0.000 description 1
- DAYNQKCWQDDZSI-UHFFFAOYSA-N (3-cyanophenyl) 4-chloro-3-nitrobenzenesulfonate Chemical compound C1=C(Cl)C([N+](=O)[O-])=CC(S(=O)(=O)OC=2C=C(C=CC=2)C#N)=C1 DAYNQKCWQDDZSI-UHFFFAOYSA-N 0.000 description 1
- ORCRRODNPXBNEA-UHFFFAOYSA-N (3-ethoxyphenyl) 4-chloro-3-nitrobenzenesulfonate Chemical compound CCOC1=CC=CC(OS(=O)(=O)C=2C=C(C(Cl)=CC=2)[N+]([O-])=O)=C1 ORCRRODNPXBNEA-UHFFFAOYSA-N 0.000 description 1
- MHCALCDTVWGUHT-UHFFFAOYSA-N (3-methoxyphenyl) 2-(methoxycarbonylamino)-3h-benzimidazole-5-sulfonate Chemical compound C1=C2NC(NC(=O)OC)=NC2=CC=C1S(=O)(=O)OC1=CC=CC(OC)=C1 MHCALCDTVWGUHT-UHFFFAOYSA-N 0.000 description 1
- VOJGRWFRPRCNEI-UHFFFAOYSA-N (4-chlorophenyl) 4-amino-3-nitrobenzenesulfonate Chemical compound C1=C([N+]([O-])=O)C(N)=CC=C1S(=O)(=O)OC1=CC=C(Cl)C=C1 VOJGRWFRPRCNEI-UHFFFAOYSA-N 0.000 description 1
- ZROLXLXBAHGRFM-UHFFFAOYSA-N (4-chlorophenyl) 4-chloro-3-nitrobenzenesulfonate Chemical compound C1=C(Cl)C([N+](=O)[O-])=CC(S(=O)(=O)OC=2C=CC(Cl)=CC=2)=C1 ZROLXLXBAHGRFM-UHFFFAOYSA-N 0.000 description 1
- WNCWVTRWQJIRLO-UHFFFAOYSA-N (4-methoxyphenyl) 4-amino-3-nitrobenzenesulfonate Chemical compound C1=CC(OC)=CC=C1OS(=O)(=O)C1=CC=C(N)C([N+]([O-])=O)=C1 WNCWVTRWQJIRLO-UHFFFAOYSA-N 0.000 description 1
- ZWEXWSDQKSCGJA-UHFFFAOYSA-N (4-methoxyphenyl) 4-chloro-3-nitrobenzenesulfonate Chemical compound C1=CC(OC)=CC=C1OS(=O)(=O)C1=CC=C(Cl)C([N+]([O-])=O)=C1 ZWEXWSDQKSCGJA-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
- SDPFJPNTJUILAT-UHFFFAOYSA-N (4-methylphenyl) 4-chloro-3-nitrobenzenesulfonate Chemical compound C1=CC(C)=CC=C1OS(=O)(=O)C1=CC=C(Cl)C([N+]([O-])=O)=C1 SDPFJPNTJUILAT-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- YOETUEMZNOLGDB-UHFFFAOYSA-N 2-methylpropyl carbonochloridate Chemical compound CC(C)COC(Cl)=O YOETUEMZNOLGDB-UHFFFAOYSA-N 0.000 description 1
- KBRSJPHSCOAFDR-UHFFFAOYSA-N 3-chloro-6-methyl-5,5-dioxo-11h-benzo[c][2,1]benzothiazepin-11-ol Chemical compound O=S1(=O)N(C)C2=CC=CC=C2C(O)C2=CC=C(Cl)C=C21 KBRSJPHSCOAFDR-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 241000893172 Chabertia Species 0.000 description 1
- 241001126268 Cooperia Species 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
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 241000243974 Haemonchus contortus Species 0.000 description 1
- 241000920462 Heterakis Species 0.000 description 1
- 241000545744 Hirudinea Species 0.000 description 1
- 241001547406 Hyostrongylus Species 0.000 description 1
- 241000510960 Oesophagostomum Species 0.000 description 1
- 241000243795 Ostertagia Species 0.000 description 1
- 241000283903 Ovis aries Species 0.000 description 1
- 208000030852 Parasitic disease Diseases 0.000 description 1
- 241000282849 Ruminantia Species 0.000 description 1
- 241000244174 Strongyloides Species 0.000 description 1
- 241000243797 Trichostrongylus Species 0.000 description 1
- 241000243796 Trichostrongylus colubriformis Species 0.000 description 1
- YUDRVAHLXDBKSR-UHFFFAOYSA-N [CH]1CCCCC1 Chemical compound [CH]1CCCCC1 YUDRVAHLXDBKSR-UHFFFAOYSA-N 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 238000010171 animal model Methods 0.000 description 1
- 230000000507 anthelmentic effect Effects 0.000 description 1
- 229940124339 anthelmintic agent Drugs 0.000 description 1
- 239000000921 anthelmintic agent Substances 0.000 description 1
- 229940058303 antinematodal benzimidazole derivative Drugs 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 150000001556 benzimidazoles Chemical class 0.000 description 1
- LMTIWZGLDGFDDI-UHFFFAOYSA-N bis(methylsulfanyl)methylidenecarbamic acid Chemical compound CSC(SC)=NC(O)=O LMTIWZGLDGFDDI-UHFFFAOYSA-N 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- 125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- SKKTUOZKZKCGTB-UHFFFAOYSA-N butyl carbamate Chemical compound CCCCOC(N)=O SKKTUOZKZKCGTB-UHFFFAOYSA-N 0.000 description 1
- NRDQFWXVTPZZAZ-UHFFFAOYSA-N butyl carbonochloridate Chemical compound CCCCOC(Cl)=O NRDQFWXVTPZZAZ-UHFFFAOYSA-N 0.000 description 1
- UIAHVZDIVLKZJB-UHFFFAOYSA-N butyl n-[bis(methylsulfanyl)methylidene]carbamate Chemical compound CCCCOC(=O)N=C(SC)SC UIAHVZDIVLKZJB-UHFFFAOYSA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 230000000973 chemotherapeutic effect Effects 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- RIFGWPKJUGCATF-UHFFFAOYSA-N ethyl chloroformate Chemical compound CCOC(Cl)=O RIFGWPKJUGCATF-UHFFFAOYSA-N 0.000 description 1
- DRQOAAZKQMGYEW-UHFFFAOYSA-N ethyl n-[bis(methylsulfanyl)methylidene]carbamate Chemical compound CCOC(=O)N=C(SC)SC DRQOAAZKQMGYEW-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 210000003608 fece Anatomy 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 239000012458 free base Substances 0.000 description 1
- 230000002496 gastric effect Effects 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 150000007529 inorganic bases Chemical class 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 210000004185 liver Anatomy 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- AKTCWMGOTIZHBA-UHFFFAOYSA-N methyl N-[butylsulfanyl(methylsulfanyl)methylidene]carbamate Chemical compound COC(=O)N=C(SCCCC)SC AKTCWMGOTIZHBA-UHFFFAOYSA-N 0.000 description 1
- YLGXILFCIXHCMC-JHGZEJCSSA-N methyl cellulose Chemical compound COC1C(OC)C(OC)C(COC)O[C@H]1O[C@H]1C(OC)C(OC)C(OC)OC1COC YLGXILFCIXHCMC-JHGZEJCSSA-N 0.000 description 1
- WOBBVXFAFLWBKA-UHFFFAOYSA-N methyl n-[(3,4-dichlorophenyl)methylsulfanyl-methylsulfanylmethylidene]carbamate Chemical compound COC(=O)N=C(SC)SCC1=CC=C(Cl)C(Cl)=C1 WOBBVXFAFLWBKA-UHFFFAOYSA-N 0.000 description 1
- YWCWHSIFIFBXDN-UHFFFAOYSA-N methyl n-[bis(butylsulfanyl)methylidene]carbamate Chemical compound CCCCSC(=NC(=O)OC)SCCCC YWCWHSIFIFBXDN-UHFFFAOYSA-N 0.000 description 1
- PCJASTSVNLHPKY-UHFFFAOYSA-N methyl n-[methylsulfanyl(phenylsulfanyl)methylidene]carbamate Chemical compound COC(=O)N=C(SC)SC1=CC=CC=C1 PCJASTSVNLHPKY-UHFFFAOYSA-N 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- OUQFCBDRFYTHKG-UHFFFAOYSA-N n-(dichloromethylidene)carbamoyl chloride Chemical compound ClC(Cl)=NC(Cl)=O OUQFCBDRFYTHKG-UHFFFAOYSA-N 0.000 description 1
- YNTOKMNHRPSGFU-UHFFFAOYSA-N n-Propyl carbamate Chemical compound CCCOC(N)=O YNTOKMNHRPSGFU-UHFFFAOYSA-N 0.000 description 1
- 239000012454 non-polar solvent Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 229940086066 potassium hydrogencarbonate Drugs 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- IVRIRQXJSNCSPQ-UHFFFAOYSA-N propan-2-yl carbonochloridate Chemical compound CC(C)OC(Cl)=O IVRIRQXJSNCSPQ-UHFFFAOYSA-N 0.000 description 1
- LANMVIAFKMWMHE-UHFFFAOYSA-N propan-2-yl n-[bis(methylsulfanyl)methylidene]carbamate Chemical compound CSC(SC)=NC(=O)OC(C)C LANMVIAFKMWMHE-UHFFFAOYSA-N 0.000 description 1
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- QQKDTTWZXHEGAQ-UHFFFAOYSA-N propyl carbonochloridate Chemical compound CCCOC(Cl)=O QQKDTTWZXHEGAQ-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- JUHMYLPYAJESKO-UHFFFAOYSA-N propyl n-[bis(methylsulfanyl)methylidene]carbamate Chemical compound CCCOC(=O)N=C(SC)SC JUHMYLPYAJESKO-UHFFFAOYSA-N 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000006798 ring closing metathesis reaction Methods 0.000 description 1
- DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 1
- 230000035938 sexual maturation Effects 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 description 1
- 239000012258 stirred mixture Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- UJJDEOLXODWCGK-UHFFFAOYSA-N tert-butyl carbonochloridate Chemical compound CC(C)(C)OC(Cl)=O UJJDEOLXODWCGK-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles 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 in position 2
- C07D235/30—Nitrogen atoms not forming part of a nitro radical
- C07D235/32—Benzimidazole-2-carbamic acids, unsubstituted or substituted; Esters thereof; Thio-analogues thereof
-
- 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2441202A DE2441202C2 (de) | 1974-08-28 | 1974-08-28 | 2-Carbalkoxyamino-benzimidazolyl-5(6)-sulfonsäure-phenylester, Verfahren zu ihrer Herstellung und diese enthaltende anthelmintische Mittel |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NO752945L NO752945L (lv) | 1976-03-02 |
| NO140592B true NO140592B (no) | 1979-06-25 |
Family
ID=5924288
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO752945A NO140592B (no) | 1974-08-28 | 1975-08-27 | Analogifremgangsmaate til fremstilling av antelmintisk virksomme 2-karbalkoksyamino-benzimidazolyl-5-(6)-sulfonsyre-fenylestere |
Country Status (30)
| Country | Link |
|---|---|
| US (2) | US3996369A (lv) |
| JP (1) | JPS5910349B2 (lv) |
| AT (1) | AT349461B (lv) |
| BE (1) | BE832858A (lv) |
| BG (3) | BG23900A3 (lv) |
| CA (1) | CA1059136A (lv) |
| CH (1) | CH611606A5 (lv) |
| CS (1) | CS196282B2 (lv) |
| DD (1) | DD122974A5 (lv) |
| DE (1) | DE2441202C2 (lv) |
| DK (1) | DK137533C (lv) |
| EG (1) | EG11811A (lv) |
| ES (1) | ES440385A1 (lv) |
| FI (1) | FI752396A (lv) |
| FR (1) | FR2282880A1 (lv) |
| GB (2) | GB1516509A (lv) |
| HU (1) | HU172144B (lv) |
| IE (1) | IE41655B1 (lv) |
| IL (1) | IL47996A (lv) |
| IT (1) | IT1041927B (lv) |
| KE (2) | KE3090A (lv) |
| LU (1) | LU73256A1 (lv) |
| MY (2) | MY8100220A (lv) |
| NL (1) | NL7509956A (lv) |
| NO (1) | NO140592B (lv) |
| PL (4) | PL101396B1 (lv) |
| SE (1) | SE417508B (lv) |
| SU (3) | SU582760A3 (lv) |
| ZA (1) | ZA755485B (lv) |
| ZM (1) | ZM12675A1 (lv) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3132167A1 (de) * | 1981-08-14 | 1983-03-03 | Hoechst Ag, 6000 Frankfurt | "5(6)-phenylsulfonyloxy-benzimidazolderivate, verfahren zu ihrer herstellung, sie enthaltende pharmazeutische zubereitungen und ihre verwendung gegen leberegel" |
| DE2608238A1 (de) * | 1976-02-28 | 1977-09-08 | Hoechst Ag | Substituierte phenylguanidine und verfahren zu ihrer herstellung |
| DE2653766A1 (de) * | 1976-11-26 | 1978-06-01 | Bayer Ag | Substituierte benzolsulfonsaeureester, verfahren zu ihrer herstellung sowie ihre verwendung als arzneimittel |
| DE2836385A1 (de) * | 1978-08-19 | 1980-03-06 | Hoechst Ag | Monocarboxylate von phenylguanidinsulfonsaeureestern, verfahren zu ihrer herstellung und ihre verwendung als arzneimittel |
| HU182782B (en) * | 1979-12-04 | 1984-03-28 | Chinoin Gyogyszer Es Vegyeszet | Process for producing alkylthio-benzimidazoles |
| DE3232959A1 (de) * | 1982-09-04 | 1984-03-08 | Hoechst Ag, 6230 Frankfurt | Substituierte benzolsulfonsaeureester, verfahren zu ihrer herstellung und ihre verwendung als arzneimittel |
| JPH0320378Y2 (lv) * | 1986-11-29 | 1991-05-01 | ||
| GB2546967B (en) | 2016-01-27 | 2020-04-15 | Thermo Fisher Scient Bremen Gmbh | Quadrupole mass spectrometer |
| GB2552841B (en) | 2016-08-12 | 2020-05-20 | Thermo Fisher Scient Bremen Gmbh | Method of calibrating a mass spectrometer |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH116815A (de) * | 1924-06-14 | 1926-09-16 | Ig Farbenindustrie Ag | Verfahren zur Darstellung des Phenylesters der 4-Nitro-1-aminobenzol-2-sulfosäure. |
| US2134642A (en) * | 1936-08-12 | 1938-10-25 | Cie Nat Matieres Colorantes | Azo dyestuff and process for the manufacture thereof |
| CH296894A (de) * | 1949-07-18 | 1954-02-28 | Ciba Geigy | Verfahren zur Herstellung eines aminogruppenhaltigen aromatischen Sulfonsäureesters. |
| BE666795A (lv) * | 1964-08-04 | 1966-01-13 | ||
| US3562290A (en) * | 1967-11-07 | 1971-02-09 | Du Pont | Process for making 2-benzimidazolecarbamic acid alkyl esters |
| BE793358A (fr) * | 1971-12-27 | 1973-06-27 | Hoechst Ag | Nouveaux derives de 2-carbalcoxy-amino-benzimidazole presentantune activite anthelmintique et leur procede de preparation |
| JPS5529110B2 (lv) * | 1972-12-25 | 1980-08-01 | ||
| ZA739219B (en) * | 1972-12-29 | 1975-07-30 | Syntex Inc | 5(6)-benzene ring substituted benzimidazole-2-carbamate derivatives having anthelmintic activity |
| US3929821A (en) * | 1972-12-29 | 1975-12-30 | Syntex Inc | 5 (6)-Benzene ring substituted benzimidazole-2-carbamate derivatives |
| US3929824A (en) * | 1972-12-29 | 1975-12-30 | Syntex Inc | 5(6)-Benzene ring substituted benzimidazole-2-carbamate derivatives having anthelmintic activity |
| US3929823A (en) * | 1973-11-21 | 1975-12-30 | Syntex Inc | 5(6)-Benzene ring substituted benzimidazole-2-carbamate derivatives having anthelmintic activity |
-
1974
- 1974-08-28 DE DE2441202A patent/DE2441202C2/de not_active Expired
-
1975
- 1975-08-15 CS CS755620A patent/CS196282B2/cs unknown
- 1975-08-18 EG EG496/75A patent/EG11811A/xx active
- 1975-08-22 NL NL7509956A patent/NL7509956A/xx not_active Application Discontinuation
- 1975-08-22 FR FR7526014A patent/FR2282880A1/fr active Granted
- 1975-08-22 ES ES440385A patent/ES440385A1/es not_active Expired
- 1975-08-23 BG BG7500031643A patent/BG23900A3/xx unknown
- 1975-08-23 BG BG7530847A patent/BG26373A3/xx unknown
- 1975-08-25 SE SE7509441A patent/SE417508B/xx unknown
- 1975-08-26 CH CH1106975A patent/CH611606A5/xx not_active IP Right Cessation
- 1975-08-26 FI FI752396A patent/FI752396A/fi not_active Application Discontinuation
- 1975-08-26 GB GB52729/77A patent/GB1516509A/en not_active Expired
- 1975-08-26 LU LU73256A patent/LU73256A1/xx unknown
- 1975-08-26 IL IL47996A patent/IL47996A/xx unknown
- 1975-08-26 US US05/608,014 patent/US3996369A/en not_active Expired - Lifetime
- 1975-08-26 ZM ZM126/75A patent/ZM12675A1/xx unknown
- 1975-08-26 GB GB35217/75A patent/GB1516508A/en not_active Expired
- 1975-08-26 IT IT26582/75A patent/IT1041927B/it active
- 1975-08-26 DD DD188028A patent/DD122974A5/xx unknown
- 1975-08-27 PL PL1975200360A patent/PL101396B1/pl unknown
- 1975-08-27 IE IE1874/75A patent/IE41655B1/en unknown
- 1975-08-27 AT AT663475A patent/AT349461B/de not_active IP Right Cessation
- 1975-08-27 NO NO752945A patent/NO140592B/no unknown
- 1975-08-27 SU SU7502167412A patent/SU582760A3/ru active
- 1975-08-27 PL PL1975200361A patent/PL100496B1/pl unknown
- 1975-08-27 PL PL1975182949A patent/PL100180B1/pl unknown
- 1975-08-27 DK DK384975A patent/DK137533C/da active
- 1975-08-27 CA CA234,273A patent/CA1059136A/en not_active Expired
- 1975-08-27 PL PL1975200362A patent/PL101537B1/pl unknown
- 1975-08-27 ZA ZA00755485A patent/ZA755485B/xx unknown
- 1975-08-28 BE BE159559A patent/BE832858A/xx not_active IP Right Cessation
- 1975-08-28 JP JP50103562A patent/JPS5910349B2/ja not_active Expired
- 1975-08-28 HU HU75HO00001832A patent/HU172144B/hu not_active IP Right Cessation
- 1975-12-01 BG BG7500031644A patent/BG25222A3/xx unknown
-
1976
- 1976-04-23 US US05/679,783 patent/US4216161A/en not_active Expired - Lifetime
- 1976-10-12 SU SU762409195A patent/SU591142A3/ru active
- 1976-10-12 SU SU762408256A patent/SU589912A3/ru active
-
1980
- 1980-10-08 KE KE3090A patent/KE3090A/xx unknown
- 1980-10-08 KE KE3089A patent/KE3089A/xx unknown
-
1981
- 1981-12-30 MY MY220/81A patent/MY8100220A/xx unknown
- 1981-12-30 MY MY222/81A patent/MY8100222A/xx unknown
Also Published As
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