SK4497A3 - Sulfonamide derivatives of azolones, method of producing, pharmaceutical composition on their base and their producing - Google Patents

Sulfonamide derivatives of azolones, method of producing, pharmaceutical composition on their base and their producing Download PDF

Info

Publication number: SK4497A3
Authority: SK; Slovakia
Prior art keywords: formula; pharmaceutically acceptable; compounds; alkyl; isomeric forms
Prior art date: 1994-07-12

Application number

SK44-97A

Other languages

English (en)

Slovak (sk)

Inventor

Jan Heeres

Raymond A Stokbroekx

Joseph H Mostmans

Der Veken Louis J E Van

Original Assignee

Janssen Pharmaceutica Nv

Priority date (The priority date 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 date listed.)

1994-07-12

Filing date

1995-07-05

Publication date

1997-12-10

1995-07-05 Application filed by Janssen Pharmaceutica Nv filed Critical Janssen Pharmaceutica Nv

1997-12-10 Publication of SK4497A3 publication Critical patent/SK4497A3/sk

Links

-1 Sulfonamide derivatives of azolones Chemical class 0.000 title claims abstract description 34
238000000034 method Methods 0.000 title claims abstract description 16
239000008194 pharmaceutical composition Substances 0.000 title claims description 11
229940124530 sulfonamide Drugs 0.000 title claims description 7
150000001875 compounds Chemical class 0.000 claims abstract description 71
150000003839 salts Chemical class 0.000 claims abstract description 22
239000001257 hydrogen Substances 0.000 claims abstract description 12
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 12
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 8
230000008569 process Effects 0.000 claims abstract description 7
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims abstract description 6
239000003814 drug Substances 0.000 claims abstract description 6
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 5
125000001475 halogen functional group Chemical group 0.000 claims abstract description 4
150000002431 hydrogen Chemical class 0.000 claims abstract description 4
125000003830 C1- C4 alkylcarbonylamino group Chemical group 0.000 claims abstract description 3
125000004786 difluoromethoxy group Chemical group [H]C(F)(F)O* 0.000 claims abstract description 3
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 3
125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims abstract description 3
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims abstract description 3
125000004356 hydroxy functional group Chemical group O* 0.000 claims abstract 2
239000002253 acid Substances 0.000 claims description 13
238000002360 preparation method Methods 0.000 claims description 9
238000006243 chemical reaction Methods 0.000 claims description 8
239000002904 solvent Substances 0.000 claims description 8
229910052736 halogen Inorganic materials 0.000 claims description 7
150000002367 halogens Chemical class 0.000 claims description 7
239000002585 base Substances 0.000 claims description 6
150000001622 bismuth compounds Chemical class 0.000 claims description 5
239000003153 chemical reaction reagent Substances 0.000 claims description 5
239000003937 drug carrier Substances 0.000 claims description 5
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
229910052757 nitrogen Inorganic materials 0.000 claims description 4
229940126409 proton pump inhibitor Drugs 0.000 claims description 4
239000000612 proton pump inhibitor Substances 0.000 claims description 4
VIXWGKYSYIBATJ-UHFFFAOYSA-N pyrrol-2-one Chemical compound O=C1C=CC=N1 VIXWGKYSYIBATJ-UHFFFAOYSA-N 0.000 claims description 4
238000004519 manufacturing process Methods 0.000 claims description 3
IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 3
125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 2
YJXHSDWITNPYFT-UHFFFAOYSA-N 2-[1-(4-chlorophenyl)-1-hydroxybutan-2-yl]-4-[6-(4-methylsulfonylpiperazin-1-yl)pyridin-3-yl]-1,2,4-triazol-3-one Chemical compound N1=CN(C=2C=NC(=CC=2)N2CCN(CC2)S(C)(=O)=O)C(=O)N1C(CC)C(O)C1=CC=C(Cl)C=C1 YJXHSDWITNPYFT-UHFFFAOYSA-N 0.000 claims description 2
HFFXLYHRNRKAPM-UHFFFAOYSA-N 2,4,5-trichloro-n-(5-methyl-1,2-oxazol-3-yl)benzenesulfonamide Chemical compound O1C(C)=CC(NS(=O)(=O)C=2C(=CC(Cl)=C(Cl)C=2)Cl)=N1 HFFXLYHRNRKAPM-UHFFFAOYSA-N 0.000 claims 6
239000003513 alkali Substances 0.000 claims 1
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 1
239000000203 mixture Substances 0.000 abstract description 30
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 42
239000000243 solution Substances 0.000 description 22
HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 15
229920000858 Cyclodextrin Polymers 0.000 description 14
241000589989 Helicobacter Species 0.000 description 14
239000004480 active ingredient Substances 0.000 description 12
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 10
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 9
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
230000000694 effects Effects 0.000 description 9
239000000543 intermediate Substances 0.000 description 9
238000012360 testing method Methods 0.000 description 8
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
238000004566 IR spectroscopy Methods 0.000 description 7
238000005481 NMR spectroscopy Methods 0.000 description 7
239000003826 tablet Substances 0.000 description 7
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
238000004949 mass spectrometry Methods 0.000 description 6
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 6
239000000725 suspension Substances 0.000 description 6
241000590002 Helicobacter pylori Species 0.000 description 5
WHGYBXFWUBPSRW-FOUAGVGXSA-N beta-cyclodextrin Chemical compound OC[C@H]([C@H]([C@@H]([C@H]1O)O)O[C@H]2O[C@@H]([C@@H](O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O3)[C@H](O)[C@H]2O)CO)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H]3O[C@@H]1CO WHGYBXFWUBPSRW-FOUAGVGXSA-N 0.000 description 5
125000004432 carbon atom Chemical group C* 0.000 description 5
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 5
239000003480 eluent Substances 0.000 description 5
229940037467 helicobacter pylori Drugs 0.000 description 5
230000002401 inhibitory effect Effects 0.000 description 5
125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 5
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 5
125000004800 4-bromophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Br 0.000 description 4
125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 description 4
125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 description 4
125000000590 4-methylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 4
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
239000002202 Polyethylene glycol Substances 0.000 description 4
229960004853 betadex Drugs 0.000 description 4
230000037396 body weight Effects 0.000 description 4
239000002775 capsule Substances 0.000 description 4
150000002170 ethers Chemical class 0.000 description 4
125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 4
TWNIBLMWSKIRAT-VFUOTHLCSA-N levoglucosan Chemical group O[C@@H]1[C@@H](O)[C@H](O)[C@H]2CO[C@@H]1O2 TWNIBLMWSKIRAT-VFUOTHLCSA-N 0.000 description 4
239000002609 medium Substances 0.000 description 4
229920001223 polyethylene glycol Polymers 0.000 description 4
238000006722 reduction reaction Methods 0.000 description 4
BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 3
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-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
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
229920002472 Starch Polymers 0.000 description 3
FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 3
239000007983 Tris buffer Substances 0.000 description 3
108010046334 Urease Proteins 0.000 description 3
230000001580 bacterial effect Effects 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
238000010790 dilution Methods 0.000 description 3
239000012895 dilution Substances 0.000 description 3
201000010099 disease Diseases 0.000 description 3
239000002552 dosage form Substances 0.000 description 3
229940080345 gamma-cyclodextrin Drugs 0.000 description 3
HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 3
125000000636 p-nitrophenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)[N+]([O-])=O 0.000 description 3
239000000843 powder Substances 0.000 description 3
239000000047 product Substances 0.000 description 3
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
230000009467 reduction Effects 0.000 description 3
235000019698 starch Nutrition 0.000 description 3
238000003756 stirring Methods 0.000 description 3
239000000126 substance Substances 0.000 description 3
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
125000000242 4-chlorobenzoyl group Chemical group ClC1=CC=C(C(=O)*)C=C1 0.000 description 2
HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 2
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
241000894006 Bacteria Species 0.000 description 2
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
239000001116 FEMA 4028 Substances 0.000 description 2
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
230000005526 G1 to G0 transition Effects 0.000 description 2
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 2
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
241001465754 Metazoa Species 0.000 description 2
AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 2
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
LCTONWCANYUPML-UHFFFAOYSA-N Pyruvic acid Chemical compound CC(=O)C(O)=O LCTONWCANYUPML-UHFFFAOYSA-N 0.000 description 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
238000004458 analytical method Methods 0.000 description 2
239000003242 anti bacterial agent Substances 0.000 description 2
230000000844 anti-bacterial effect Effects 0.000 description 2
229940088710 antibiotic agent Drugs 0.000 description 2
239000012298 atmosphere Substances 0.000 description 2
CSKNSYBAZOQPLR-UHFFFAOYSA-N benzenesulfonyl chloride Chemical compound ClS(=O)(=O)C1=CC=CC=C1 CSKNSYBAZOQPLR-UHFFFAOYSA-N 0.000 description 2
235000011175 beta-cyclodextrine Nutrition 0.000 description 2
239000006161 blood agar Substances 0.000 description 2
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125000005843 halogen group Chemical group 0.000 description 2
238000000338 in vitro Methods 0.000 description 2
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
235000014655 lactic acid Nutrition 0.000 description 2
239000008101 lactose Substances 0.000 description 2
239000007788 liquid Substances 0.000 description 2
229910052987 metal hydride Inorganic materials 0.000 description 2
125000004433 nitrogen atom Chemical group N* 0.000 description 2
231100000252 nontoxic Toxicity 0.000 description 2
230000003000 nontoxic effect Effects 0.000 description 2
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229910052700 potassium Inorganic materials 0.000 description 2
239000002244 precipitate Substances 0.000 description 2
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YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
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JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
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MDTUWBLTRPRXBX-UHFFFAOYSA-N 1,2,4-triazol-3-one Chemical compound O=C1N=CN=N1 MDTUWBLTRPRXBX-UHFFFAOYSA-N 0.000 description 1
QBWLKDFBINPHFT-UHFFFAOYSA-L 1,3,2$l^{2}-benzodioxabismin-4-one;hydrate Chemical compound O.C1=CC=C2C(=O)O[Bi]OC2=C1 QBWLKDFBINPHFT-UHFFFAOYSA-L 0.000 description 1
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
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Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D249/12—Oxygen or sulfur atoms

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General Chemical & Material Sciences (AREA)
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Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
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Bioinformatics & Cheminformatics (AREA)
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Communicable Diseases (AREA)
Oncology (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Plural Heterocyclic Compounds (AREA)
Steroid Compounds (AREA)
Cephalosporin Compounds (AREA)
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SK44-97A 1994-07-12 1995-07-05 Sulfonamide derivatives of azolones, method of producing, pharmaceutical composition on their base and their producing SK4497A3 (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
EP94202015		1994-07-12
PCT/EP1995/002619 WO1996001818A1 (en)	1994-07-12	1995-07-05	Sulfonamide derivatives of azolones anti-helicobacter agents

Publications (1)

Publication Number	Publication Date
SK4497A3 true SK4497A3 (en)	1997-12-10

Family

ID=8217029

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK44-97A SK4497A3 (en)	1994-07-12	1995-07-05	Sulfonamide derivatives of azolones, method of producing, pharmaceutical composition on their base and their producing

Country Status (21)

Country	Link
US (2)	US5571811A (fi)
EP (1)	EP0770071B1 (fi)
JP (1)	JPH10502386A (fi)
CN (1)	CN1068878C (fi)
AT (1)	ATE206706T1 (fi)
AU (1)	AU684981B2 (fi)
BR (1)	BR9508376A (fi)
CA (1)	CA2194562A1 (fi)
CZ (1)	CZ2997A3 (fi)
DE (1)	DE69523159T2 (fi)
FI (1)	FI970113A0 (fi)
HU (1)	HUT76636A (fi)
IL (1)	IL114537A (fi)
MX (1)	MX9700340A (fi)
NO (1)	NO970089L (fi)
NZ (1)	NZ289853A (fi)
PL (1)	PL318149A1 (fi)
SK (1)	SK4497A3 (fi)
TW (1)	TW341571B (fi)
WO (1)	WO1996001818A1 (fi)
ZA (1)	ZA955760B (fi)

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* Cited by examiner, † Cited by third party
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US5639754A (en) *	1994-07-12	1997-06-17	Janssen Pharmaceutica N.V.	Urea and thiourea derivatives of azolones
US5637592A (en) *	1994-07-12	1997-06-10	Janssen Pharmaceutica N.V.	Acyl derivatives of azolones
US5571811A (en) *	1994-07-12	1996-11-05	Janssen Pharmaceutica N.V.	Sulfonamide derivatives of azolones
DE60033019D1 (de)	1999-03-17	2007-03-08	Morinaga & Co	Arzneimittel, nahrungsmittel, getränke und futter enthaltend eine kakao-komponente
US6780880B1 (en)	1999-08-26	2004-08-24	Robert R. Whittle	FT-Raman spectroscopic measurement
US6369087B1 (en)	1999-08-26	2002-04-09	Robert R. Whittle	Alkoxy substituted benzimidazole compounds, pharmaceutical preparations containing the same, and methods of using the same
US6262085B1 (en)	1999-08-26	2001-07-17	Robert R. Whittle	Alkoxy substituted Benzimidazole compounds, pharmaceutical preparations containing the same, and methods of using the same
US6326384B1 (en)	1999-08-26	2001-12-04	Robert R. Whittle	Dry blend pharmaceutical unit dosage form
US6312723B1 (en)	1999-08-26	2001-11-06	Robert R. Whittle	Pharmaceutical unit dosage form
US6268385B1 (en)	1999-08-26	2001-07-31	Robert R. Whittle	Dry blend pharmaceutical formulations
US6312712B1 (en)	1999-08-26	2001-11-06	Robert R. Whittle	Method of improving bioavailability
US6262086B1 (en)	1999-08-26	2001-07-17	Robert R. Whittle	Pharmaceutical unit dosage form
US6316020B1 (en)	1999-08-26	2001-11-13	Robert R. Whittle	Pharmaceutical formulations
US20050119251A1 (en) *	2001-12-21	2005-06-02	Jian-Min Fu	Nicotinamide derivatives and their use as therapeutic agents
DK1563061T3 (da) *	2002-11-14	2012-10-01	Aderans Res Inst Inc	Dyrkning af hårinducerende celler
US8013156B2 (en) *	2003-03-19	2011-09-06	Exelixis, Inc.	Tie-2 modulators and methods of use
EP2316457A1 (en) *	2004-09-20	2011-05-04	Xenon Pharmaceuticals Inc.	Pyridine derivatives for inhibiting human stearoyl-coa-desaturase
WO2006034441A1 (en) *	2004-09-20	2006-03-30	Xenon Pharmaceuticals Inc.	Heterocyclic derivatives and their use as stearoyl-coa desaturase inhibitors
MX2007003319A (es) *	2004-09-20	2007-06-05	Xenon Pharmaceuticals Inc	Derivados heterociclicos y su uso como agentes terapeuticos.
US7919496B2 (en)	2004-09-20	2011-04-05	Xenon Pharmaceuticals Inc.	Heterocyclic derivatives for the treatment of diseases mediated by stearoyl-CoA desaturase enzymes
JP4958785B2 (ja)	2004-09-20	2012-06-20	ゼノン・ファーマシューティカルズ・インコーポレイテッド	複素環誘導体およびステアロイル−ＣｏＡデサチュラーゼインヒビターとしてのそれらの使用
CA2580781A1 (en) *	2004-09-20	2006-03-30	Xenon Pharmaceuticals Inc.	Bicyclic heterocyclic derivatives and their use as inhibitors of stearoyl-coa-desaturase (scd)
AU2005286728A1 (en) *	2004-09-20	2006-03-30	Xenon Pharmaceuticals Inc.	Heterocyclic derivatives and their use as mediators of stearoyl-CoA desaturase
MX2007003321A (es)	2004-09-20	2007-06-05	Xenon Pharmaceuticals Inc	Derivados heterociclicos y su uso como agentes terapeuticos.
AU2005286647A1 (en)	2004-09-20	2006-03-30	Xenon Pharmaceuticals Inc.	Heterocyclic derivatives and their use as stearoyl-CoA desaturase inhibitors
CA2618646A1 (en)	2005-06-03	2007-11-15	Xenon Pharmaceuticals Inc.	Aminothiazole derivatives as human stearoyl-coa desaturase inhibitors
JP2022516571A (ja) *	2019-01-06	2022-02-28	プソマーゲン，インコーポレイテッド	Ｈｔｒａ阻害物質及びｃａｇａ阻害物質並びに同物質の使用

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CA1292472C (en) *	1985-12-03	1991-11-26	Alfonsus Guilielmus Knaeps	Derivatives of ¬¬4-¬4-(4-phenyl-1-piperazinyl)- phenoxymethyl\|-1,3-dioxolan-2-yl\|methyl\|-1h-imidazoles and 1h-1,2,4-triazoles
US4791111A (en) *	1985-12-23	1988-12-13	Janssen Pharmaceutica, N.V.	[[4-[4-(4-phenyl-1-piperazinyl)phenoxymethyl]-1,3-dioxolan-2-yl]methyl]-1H-imidazoles and 1H-1,2,4-triazoles having anti-microbial properties
CA1331757C (en) *	1988-02-29	1994-08-30	Janssen Pharmaceutica Naamloze Vennootschap	5-lipoxygenase inhibiting 4-(4-phenyl-1-piperazinyl)phenols
CA2076257A1 (en) *	1991-09-13	1993-03-14	Jan Heeres	4-¬4-¬4-(4-hydroxyphenyl)-1- piperazinyl\|phenyl\|-5-methyl-3h -1,2,4-triazol-3-one derivatives
US5571811A (en) *	1994-07-12	1996-11-05	Janssen Pharmaceutica N.V.	Sulfonamide derivatives of azolones

1995
- 1995-05-23 US US08/447,505 patent/US5571811A/en not_active Expired - Fee Related
- 1995-05-25 TW TW084105259A patent/TW341571B/zh active
- 1995-07-05 MX MX9700340A patent/MX9700340A/es unknown
- 1995-07-05 DE DE69523159T patent/DE69523159T2/de not_active Expired - Fee Related
- 1995-07-05 EP EP95925838A patent/EP0770071B1/en not_active Expired - Lifetime
- 1995-07-05 WO PCT/EP1995/002619 patent/WO1996001818A1/en active IP Right Grant
- 1995-07-05 AT AT95925838T patent/ATE206706T1/de not_active IP Right Cessation
- 1995-07-05 CZ CZ9729A patent/CZ2997A3/cs unknown
- 1995-07-05 HU HU9700080A patent/HUT76636A/hu unknown
- 1995-07-05 CN CN95194022A patent/CN1068878C/zh not_active Expired - Fee Related
- 1995-07-05 BR BR9508376A patent/BR9508376A/pt unknown
- 1995-07-05 PL PL95318149A patent/PL318149A1/xx unknown
- 1995-07-05 JP JP8504112A patent/JPH10502386A/ja active Pending
- 1995-07-05 SK SK44-97A patent/SK4497A3/sk unknown
- 1995-07-05 US US08/776,003 patent/US5728700A/en not_active Expired - Fee Related
- 1995-07-05 CA CA002194562A patent/CA2194562A1/en not_active Abandoned
- 1995-07-05 AU AU29819/95A patent/AU684981B2/en not_active Ceased
- 1995-07-11 IL IL11453795A patent/IL114537A/xx active IP Right Grant
- 1995-07-11 ZA ZA955760A patent/ZA955760B/xx unknown
1997
- 1997-01-08 NZ NZ289853A patent/NZ289853A/en unknown
- 1997-01-09 NO NO970089A patent/NO970089L/no not_active Application Discontinuation
- 1997-01-10 FI FI970113A patent/FI970113A0/fi unknown

Also Published As

Publication number	Publication date
US5571811A (en)	1996-11-05
NZ289853A (en)	1997-11-24
MX9700340A (es)	1997-05-31
PL318149A1 (en)	1997-05-12
NO970089L (no)	1997-03-10
ZA955760B (en)	1997-01-13
CN1068878C (zh)	2001-07-25
DE69523159T2 (de)	2002-06-20
AU2981995A (en)	1996-02-09
DE69523159D1 (de)	2001-11-15
FI970113L (fi)	1997-01-10
EP0770071A1 (en)	1997-05-02
CN1152308A (zh)	1997-06-18
CA2194562A1 (en)	1996-01-25
HUT76636A (en)	1997-10-28
IL114537A (en)	1999-04-11
IL114537A0 (en)	1995-11-27
TW341571B (en)	1998-10-01
JPH10502386A (ja)	1998-03-03
ATE206706T1 (de)	2001-10-15
AU684981B2 (en)	1998-01-08
US5728700A (en)	1998-03-17
BR9508376A (pt)	1997-10-28
WO1996001818A1 (en)	1996-01-25
NO970089D0 (no)	1997-01-09
FI970113A0 (fi)	1997-01-10
CZ2997A3 (en)	1997-09-17
EP0770071B1 (en)	2001-10-10
HU9700080D0 (en)	1997-02-28

Publication	Publication Date	Title
SK4497A3 (en)	1997-12-10	Sulfonamide derivatives of azolones, method of producing, pharmaceutical composition on their base and their producing
US5639754A (en)	1997-06-17	Urea and thiourea derivatives of azolones
SK4397A3 (en)	1997-11-05	Acyl azolones, manufacturing process thereof, pharmauceutical compositions on their base and process for producing them
PL174836B1 (pl)	1998-09-30	Wykazujące działanie przeciwko bakteriom Helicobacter nowe podstawione pochodne azolonu i sposób wytwarzania podstawionych pochodnych azolonu
US5607932A (en)	1997-03-04	Heterocyclic derivatives of azolones
US5710156A (en)	1998-01-20	Ester and carbamate derivatives of azolones
CZ287159B6 (en)	2000-10-11	4-Quinolyl derivatives per se and for use as medicaments, process of their preparation and pharmaceutical preparations based thereon
EP0770072A1 (en)	1997-05-02	Anti-helicobacter urea and thiourea derivatives of azolones
MXPA96004610A (en)	1998-07-03	Ester derivatives and anti-helicobac azolone carbamate