ZA200405941B - R-(-)-1-Ä2-(7-Chloro-benzo ÄbÜ thiophen-3-yl-methoxy) -2- (2,4-dichloro-phenyl) -ethylÜ-1H-imidazole - Google Patents
R-(-)-1-Ä2-(7-Chloro-benzo ÄbÜ thiophen-3-yl-methoxy) -2- (2,4-dichloro-phenyl) -ethylÜ-1H-imidazole Download PDFInfo
- Publication number
- ZA200405941B ZA200405941B ZA200405941A ZA200405941A ZA200405941B ZA 200405941 B ZA200405941 B ZA 200405941B ZA 200405941 A ZA200405941 A ZA 200405941A ZA 200405941 A ZA200405941 A ZA 200405941A ZA 200405941 B ZA200405941 B ZA 200405941B
- Authority
- ZA
- South Africa
- Prior art keywords
- dichlorophenyl
- methoxy
- imidazole
- chlorobenzo
- ethyl
- Prior art date
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- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Substances C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 title claims description 10
- -1 thiophen-3-yl-methoxy Chemical group 0.000 title claims description 8
- 125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 title claims 6
- 239000000203 mixture Substances 0.000 claims abstract description 17
- 238000000034 method Methods 0.000 claims abstract description 11
- 150000003839 salts Chemical class 0.000 claims abstract description 11
- 238000002360 preparation method Methods 0.000 claims abstract description 10
- 201000010099 disease Diseases 0.000 claims abstract description 7
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 7
- 241001465754 Metazoa Species 0.000 claims abstract description 5
- JLGKQTAYUIMGRK-IBGZPJMESA-N arasertaconazole Chemical compound ClC1=CC(Cl)=CC=C1[C@@H](OCC=1C2=CC=CC(Cl)=C2SC=1)CN1C=NC=C1 JLGKQTAYUIMGRK-IBGZPJMESA-N 0.000 claims abstract description 5
- 206010017533 Fungal infection Diseases 0.000 claims abstract description 4
- 208000031888 Mycoses Diseases 0.000 claims abstract description 4
- 150000001875 compounds Chemical class 0.000 claims description 7
- UKVLTPAGJIYSGN-NSHDSACASA-N (1r)-1-(2,4-dichlorophenyl)-2-imidazol-1-ylethanol Chemical compound C([C@H](O)C=1C(=CC(Cl)=CC=1)Cl)N1C=CN=C1 UKVLTPAGJIYSGN-NSHDSACASA-N 0.000 claims description 5
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 4
- 229910017604 nitric acid Inorganic materials 0.000 claims description 4
- 239000008194 pharmaceutical composition Substances 0.000 claims description 4
- YAEYBUZMILPYLT-UHFFFAOYSA-N 1-(2,4-dichlorophenyl)-2-imidazol-1-ylethanone Chemical compound ClC1=CC(Cl)=CC=C1C(=O)CN1C=NC=C1 YAEYBUZMILPYLT-UHFFFAOYSA-N 0.000 claims description 3
- HAAITRDZHUANGT-FYZYNONXSA-N arasertaconazole nitrate Chemical compound O[N+]([O-])=O.ClC1=CC(Cl)=CC=C1[C@@H](OCC=1C2=CC=CC(Cl)=C2SC=1)CN1C=NC=C1 HAAITRDZHUANGT-FYZYNONXSA-N 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 239000000460 chlorine Substances 0.000 claims 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
- 229910052794 bromium Chemical group 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 150000002367 halogens Chemical group 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 21
- 229960005429 sertaconazole Drugs 0.000 description 19
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 18
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 15
- 239000000243 solution Substances 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- JLGKQTAYUIMGRK-UHFFFAOYSA-N 1-{2-[(7-chloro-1-benzothiophen-3-yl)methoxy]-2-(2,4-dichlorophenyl)ethyl}imidazole Chemical compound ClC1=CC(Cl)=CC=C1C(OCC=1C2=CC=CC(Cl)=C2SC=1)CN1C=NC=C1 JLGKQTAYUIMGRK-UHFFFAOYSA-N 0.000 description 12
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 10
- 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 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N EtOH Substances CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
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- 241000233866 Fungi Species 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 240000004808 Saccharomyces cerevisiae Species 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
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- NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
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- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 2
- 239000002775 capsule Substances 0.000 description 2
- 229960001631 carbomer Drugs 0.000 description 2
- PSEHHVRCDVOTID-VMAIWCPRSA-N chloro-bis[(1r,3r,4s,5r)-4,6,6-trimethyl-3-bicyclo[3.1.1]heptanyl]borane Chemical compound C([C@H]([C@@H]1C)B(Cl)[C@H]2[C@H](C)[C@]3(C[C@@](C2)(C3(C)C)[H])[H])[C@@]2([H])C(C)(C)[C@]1([H])C2 PSEHHVRCDVOTID-VMAIWCPRSA-N 0.000 description 2
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- 239000012153 distilled water Substances 0.000 description 2
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- 238000009472 formulation Methods 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 239000006210 lotion Substances 0.000 description 2
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
- 239000012299 nitrogen atmosphere Substances 0.000 description 2
- 239000002674 ointment Substances 0.000 description 2
- 239000012044 organic layer Substances 0.000 description 2
- 239000006072 paste Substances 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 2
- QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000003826 tablet Substances 0.000 description 2
- 229930192474 thiophene Natural products 0.000 description 2
- UKVLTPAGJIYSGN-LLVKDONJSA-N (1s)-1-(2,4-dichlorophenyl)-2-imidazol-1-ylethanol Chemical compound C([C@@H](O)C=1C(=CC(Cl)=CC=1)Cl)N1C=CN=C1 UKVLTPAGJIYSGN-LLVKDONJSA-N 0.000 description 1
- YONLFQNRGZXBBF-ZIAGYGMSSA-N (2r,3r)-2,3-dibenzoyloxybutanedioic acid Chemical compound O([C@@H](C(=O)O)[C@@H](OC(=O)C=1C=CC=CC=1)C(O)=O)C(=O)C1=CC=CC=C1 YONLFQNRGZXBBF-ZIAGYGMSSA-N 0.000 description 1
- HAAITRDZHUANGT-FSRHSHDFSA-N (S)-sertaconazole nitrate Chemical compound O[N+]([O-])=O.ClC1=CC(Cl)=CC=C1[C@H](OCC=1C2=CC=CC(Cl)=C2SC=1)CN1C=NC=C1 HAAITRDZHUANGT-FSRHSHDFSA-N 0.000 description 1
- UKVLTPAGJIYSGN-UHFFFAOYSA-N 1-(2,4-dichlorophenyl)-2-imidazol-1-ylethanol Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(O)CN1C=CN=C1 UKVLTPAGJIYSGN-UHFFFAOYSA-N 0.000 description 1
- UEKUFHQHXAAMLQ-UHFFFAOYSA-N 1-imidazol-1-ylethanol Chemical compound CC(O)N1C=CN=C1 UEKUFHQHXAAMLQ-UHFFFAOYSA-N 0.000 description 1
- GPOFRJKTYRFQLJ-UHFFFAOYSA-N 2-aminoethanol;undec-10-enoic acid Chemical compound NCCO.OC(=O)CCCCCCCCC=C GPOFRJKTYRFQLJ-UHFFFAOYSA-N 0.000 description 1
- QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 description 1
- LXAHHHIGZXPRKQ-UHFFFAOYSA-N 5-fluoro-2-methylpyridine Chemical compound CC1=CC=C(F)C=N1 LXAHHHIGZXPRKQ-UHFFFAOYSA-N 0.000 description 1
- WYLPACACKSNLES-UHFFFAOYSA-N 7-chloro-3-(chloromethyl)-1-benzothiophene Chemical compound C1=CC=C2C(CCl)=CSC2=C1Cl WYLPACACKSNLES-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
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- 229920001213 Polysorbate 20 Polymers 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 229940121375 antifungal agent Drugs 0.000 description 1
- 239000003429 antifungal agent Substances 0.000 description 1
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- 230000004071 biological effect Effects 0.000 description 1
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- SASYSVUEVMOWPL-NXVVXOECSA-N decyl oleate Chemical compound CCCCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC SASYSVUEVMOWPL-NXVVXOECSA-N 0.000 description 1
- WGLUMOCWFMKWIL-UHFFFAOYSA-N dichloromethane;methanol Chemical compound OC.ClCCl WGLUMOCWFMKWIL-UHFFFAOYSA-N 0.000 description 1
- 125000004188 dichlorophenyl group Chemical group 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
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- 229940079593 drug Drugs 0.000 description 1
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- IDGUHHHQCWSQLU-UHFFFAOYSA-N ethanol;hydrate Chemical compound O.CCO IDGUHHHQCWSQLU-UHFFFAOYSA-N 0.000 description 1
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- FEWJPZIEWOKRBE-LWMBPPNESA-N levotartaric acid Chemical compound OC(=O)[C@@H](O)[C@H](O)C(O)=O FEWJPZIEWOKRBE-LWMBPPNESA-N 0.000 description 1
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 1
- 239000004292 methyl p-hydroxybenzoate Substances 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 229960002216 methylparaben Drugs 0.000 description 1
- 230000002906 microbiologic effect Effects 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- 230000017066 negative regulation of growth Effects 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
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- 229960005323 phenoxyethanol Drugs 0.000 description 1
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 1
- 235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 1
- 239000004405 propyl p-hydroxybenzoate Substances 0.000 description 1
- 229960003415 propylparaben Drugs 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
-
- 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
-
- 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
- A61P31/10—Antimycotics
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ES200200328A ES2203316B1 (es) | 2002-02-11 | 2002-02-11 | R-(-)-1-(2-(7-cloro-benzo(b)tiofen-3-il-metoxi)-2-(2,4-dicloro-fenil)-etil)1h-imidazol. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200405941B true ZA200405941B (en) | 2006-07-26 |
Family
ID=27675919
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200405941A ZA200405941B (en) | 2002-02-11 | 2004-07-26 | R-(-)-1-Ä2-(7-Chloro-benzo ÄbÜ thiophen-3-yl-methoxy) -2- (2,4-dichloro-phenyl) -ethylÜ-1H-imidazole |
Country Status (25)
| Country | Link |
|---|---|
| US (1) | US7323433B2 (es) |
| EP (1) | EP1474422B1 (es) |
| JP (1) | JP5095070B2 (es) |
| KR (1) | KR100701457B1 (es) |
| CN (1) | CN1315824C (es) |
| AT (1) | ATE382618T1 (es) |
| AU (1) | AU2003205733B8 (es) |
| BR (1) | BR0307754A (es) |
| CA (1) | CA2474627C (es) |
| CO (1) | CO5601026A2 (es) |
| DE (1) | DE60318395T2 (es) |
| DK (1) | DK1474422T3 (es) |
| ES (1) | ES2203316B1 (es) |
| HK (1) | HK1070883A1 (es) |
| IL (1) | IL163452A (es) |
| MX (1) | MXPA04007581A (es) |
| NO (1) | NO327937B1 (es) |
| NZ (1) | NZ534464A (es) |
| PL (1) | PL211168B1 (es) |
| PT (1) | PT1474422E (es) |
| RU (1) | RU2276152C1 (es) |
| TN (1) | TNSN04140A1 (es) |
| UA (1) | UA78010C2 (es) |
| WO (1) | WO2003068770A1 (es) |
| ZA (1) | ZA200405941B (es) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2249992B1 (es) | 2004-09-13 | 2007-03-01 | Ferrer Internacional, S.A. | Un procedimiento para fabricar compuestos enantiomericos del imidazol. |
| ES2249991B1 (es) * | 2004-09-13 | 2007-03-01 | Ferrer Internacional, S.A. | Procedimiento de fabricacion de compuestos imidazolicos, sus sales y sus pseudopolimorfos. |
| EP1698336A1 (en) * | 2005-03-01 | 2006-09-06 | Ferrer Internacional, S.A. | Antifungal compositions comprising Sertaconazole and either Hydrocortisone or an antibacterial agent |
| RU2477280C1 (ru) * | 2008-12-09 | 2013-03-10 | Феррер Интернасионал С.А. | Полиморфная модификация ii противогрибкового соединения, способ ее получения (варианты), фармацевтическая и сельскохозяйственная композиции на ее основе, способ лечения или профилактики заболеваний, вызванных грибками и/или дрожжами |
| EP2436374A1 (en) * | 2010-09-30 | 2012-04-04 | Ferrer Internacional, S.A. | Ovule for vaginal administration of arasertaconazole |
| EP2551351A1 (en) | 2011-07-29 | 2013-01-30 | Interquim, S.A. | Process for production of optically active (R)-(-)-1-(2,4-dichloro-phenyl)-2-imidazole-1-yl-ethanol |
| CN102440947B (zh) * | 2011-11-15 | 2012-12-26 | 海南海神同洲制药有限公司 | 硝酸舍他康唑乳膏剂 |
| KR101717968B1 (ko) | 2016-07-18 | 2017-03-20 | 씨앤아이 주식회사 | 스마트폰 결합 모듈 |
| CN113480517B (zh) * | 2021-07-30 | 2022-09-09 | 海南海神同洲制药有限公司 | 3-溴甲基-7-氯苯并[b]噻吩的合成方法 |
| CN113735843B (zh) * | 2021-09-07 | 2023-05-26 | 海南海神同洲制药有限公司 | 一种低熔点硝酸舍他康唑的制备方法 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA1250586A (en) * | 1984-02-02 | 1989-02-28 | Manuel Raga | 1h-imidazole derivatives and process for their production |
| US5135943A (en) * | 1984-02-02 | 1992-08-04 | Ferrer Internacional S.A. | 1H-imidazole derivative compounds and pharmaceutical compositions containing the same |
| US5087620A (en) * | 1990-05-17 | 1992-02-11 | Bristol-Myers Squibb Co. | Controlled dermal penetration enhancement using imidazoles |
| AU691234B2 (en) * | 1995-01-04 | 1998-05-14 | Ferrer Internacional, S.A. | Process for preparing polymorphs B and C of 1- 2,4-dichloro -beta- (7-chlorobenzo b thien-3-yl)methoxy phenethyl imidazole mononitrate |
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2002
- 2002-02-11 ES ES200200328A patent/ES2203316B1/es not_active Expired - Fee Related
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- 2003-02-04 CN CNB038036592A patent/CN1315824C/zh not_active Expired - Fee Related
- 2003-02-04 MX MXPA04007581A patent/MXPA04007581A/es active IP Right Grant
- 2003-02-04 CA CA002474627A patent/CA2474627C/en not_active Expired - Fee Related
- 2003-02-04 BR BR0307754-3A patent/BR0307754A/pt not_active IP Right Cessation
- 2003-02-04 KR KR1020047012352A patent/KR100701457B1/ko not_active IP Right Cessation
- 2003-02-04 NZ NZ534464A patent/NZ534464A/en not_active IP Right Cessation
- 2003-02-04 EP EP03702597A patent/EP1474422B1/en not_active Expired - Lifetime
- 2003-02-04 JP JP2003567897A patent/JP5095070B2/ja not_active Expired - Fee Related
- 2003-02-04 RU RU2004127573/04A patent/RU2276152C1/ru not_active IP Right Cessation
- 2003-02-04 PL PL370251A patent/PL211168B1/pl unknown
- 2003-02-04 PT PT03702597T patent/PT1474422E/pt unknown
- 2003-02-04 DE DE60318395T patent/DE60318395T2/de not_active Expired - Lifetime
- 2003-02-04 DK DK03702597T patent/DK1474422T3/da active
- 2003-02-04 WO PCT/EP2003/001089 patent/WO2003068770A1/en active IP Right Grant
- 2003-02-04 AT AT03702597T patent/ATE382618T1/de active
- 2003-02-04 AU AU2003205733A patent/AU2003205733B8/en not_active Ceased
- 2003-04-02 UA UA20040806675A patent/UA78010C2/uk unknown
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2004
- 2004-07-26 ZA ZA200405941A patent/ZA200405941B/en unknown
- 2004-07-29 TN TNP2004000140A patent/TNSN04140A1/en unknown
- 2004-08-05 US US10/911,572 patent/US7323433B2/en not_active Expired - Fee Related
- 2004-08-06 CO CO04076775A patent/CO5601026A2/es not_active Application Discontinuation
- 2004-08-10 IL IL163452A patent/IL163452A/en not_active IP Right Cessation
- 2004-08-13 NO NO20043377A patent/NO327937B1/no not_active IP Right Cessation
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