SU1586513A3 - Способ получени производных 2-алкилбензимидазола - Google Patents
Способ получени производных 2-алкилбензимидазола Download PDFInfo
- Publication number
- SU1586513A3 SU1586513A3 SU874028881A SU4028881A SU1586513A3 SU 1586513 A3 SU1586513 A3 SU 1586513A3 SU 874028881 A SU874028881 A SU 874028881A SU 4028881 A SU4028881 A SU 4028881A SU 1586513 A3 SU1586513 A3 SU 1586513A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- eleven
- well
- hydrogen
- compound
- joint venture
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 36
- 229910052739 hydrogen Inorganic materials 0.000 claims description 26
- 239000001257 hydrogen Substances 0.000 claims description 26
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 18
- 150000002431 hydrogen Chemical class 0.000 claims description 17
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 14
- 238000002360 preparation method Methods 0.000 claims description 11
- 239000000203 mixture Substances 0.000 claims description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 5
- 229910052717 sulfur Inorganic materials 0.000 claims description 5
- NHQDETIJWKXCTC-UHFFFAOYSA-N 3-chloroperbenzoic acid Chemical compound OOC(=O)C1=CC=CC(Cl)=C1 NHQDETIJWKXCTC-UHFFFAOYSA-N 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 4
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- 230000003647 oxidation Effects 0.000 claims description 4
- 238000007254 oxidation reaction Methods 0.000 claims description 4
- 239000011593 sulfur Substances 0.000 claims description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid group Chemical class S(O)(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 3
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 claims description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
- 125000000815 N-oxide group Chemical group 0.000 claims description 2
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 2
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052794 bromium Inorganic materials 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 239000000460 chlorine Substances 0.000 claims description 2
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 claims description 2
- 229910052731 fluorine Inorganic materials 0.000 claims description 2
- 239000011737 fluorine Substances 0.000 claims description 2
- 210000004051 gastric juice Anatomy 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- 230000002401 inhibitory effect Effects 0.000 claims description 2
- 230000028327 secretion Effects 0.000 claims description 2
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 2
- 101100123850 Caenorhabditis elegans her-1 gene Proteins 0.000 claims 2
- 229910052740 iodine Inorganic materials 0.000 claims 2
- SUBDBMMJDZJVOS-UHFFFAOYSA-N 5-methoxy-2-{[(4-methoxy-3,5-dimethylpyridin-2-yl)methyl]sulfinyl}-1H-benzimidazole Chemical compound N=1C2=CC(OC)=CC=C2NC=1S(=O)CC1=NC=C(C)C(OC)=C1C SUBDBMMJDZJVOS-UHFFFAOYSA-N 0.000 claims 1
- 241000382509 Vania Species 0.000 claims 1
- 230000009858 acid secretion Effects 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 150000001350 alkyl halides Chemical class 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 claims 1
- 125000001153 fluoro group Chemical group F* 0.000 claims 1
- 238000002955 isolation Methods 0.000 claims 1
- 229960000381 omeprazole Drugs 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 abstract description 3
- 229940058303 antinematodal benzimidazole derivative Drugs 0.000 abstract 1
- 125000003785 benzimidazolyl group Chemical class N1=C(NC2=C1C=CC=C2)* 0.000 abstract 1
- 229940126601 medicinal product Drugs 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 18
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 10
- -1 2-benzimidazolylmethylthio Chemical group 0.000 description 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 7
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 6
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 6
- 229910052938 sodium sulfate Inorganic materials 0.000 description 6
- 235000011152 sodium sulphate Nutrition 0.000 description 6
- 239000012074 organic phase Substances 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-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
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 229910000029 sodium carbonate Inorganic materials 0.000 description 3
- HIJDNBHIZBRNSX-UHFFFAOYSA-N 5,6-dimethyl-2-(pyridin-2-ylsulfanylmethyl)-1h-benzimidazole Chemical compound N1C=2C=C(C)C(C)=CC=2N=C1CSC1=CC=CC=N1 HIJDNBHIZBRNSX-UHFFFAOYSA-N 0.000 description 2
- FKXZKCKMHPDLFD-UHFFFAOYSA-N 6-chloro-2-(pyridin-2-ylsulfanylmethyl)-1h-benzimidazole Chemical compound N1C2=CC(Cl)=CC=C2N=C1CSC1=CC=CC=N1 FKXZKCKMHPDLFD-UHFFFAOYSA-N 0.000 description 2
- MXNSJRIWFAPKAV-UHFFFAOYSA-N 6-chloro-2-(pyridin-2-ylsulfonylmethyl)-1h-benzimidazole Chemical compound N1C2=CC(Cl)=CC=C2N=C1CS(=O)(=O)C1=CC=CC=N1 MXNSJRIWFAPKAV-UHFFFAOYSA-N 0.000 description 2
- 229920000084 Gum arabic Polymers 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- 241000700159 Rattus Species 0.000 description 2
- 241000978776 Senegalia senegal Species 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- YCBGWNSBVGWSQL-UHFFFAOYSA-N [1-methyl-2-(pyridin-2-ylsulfinylmethyl)benzimidazol-5-yl]-phenylmethanone Chemical compound N=1C2=CC(C(=O)C=3C=CC=CC=3)=CC=C2N(C)C=1CS(=O)C1=CC=CC=N1 YCBGWNSBVGWSQL-UHFFFAOYSA-N 0.000 description 2
- 230000003187 abdominal effect Effects 0.000 description 2
- 239000000205 acacia gum Substances 0.000 description 2
- 235000010489 acacia gum Nutrition 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 230000002496 gastric effect Effects 0.000 description 2
- 230000005764 inhibitory process Effects 0.000 description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
- GBLKUQWHCVUFFE-UHFFFAOYSA-N phenyl-[2-(pyridin-2-ylsulfanylmethyl)-3h-benzimidazol-5-yl]methanone Chemical compound C=1C=C2N=C(CSC=3N=CC=CC=3)NC2=CC=1C(=O)C1=CC=CC=C1 GBLKUQWHCVUFFE-UHFFFAOYSA-N 0.000 description 2
- YUMLCCPUFPMTEI-UHFFFAOYSA-N phenyl-[2-(pyridin-2-ylsulfinylmethyl)-3h-benzimidazol-5-yl]methanone Chemical compound C=1C=C2N=C(CS(=O)C=3N=CC=CC=3)NC2=CC=1C(=O)C1=CC=CC=C1 YUMLCCPUFPMTEI-UHFFFAOYSA-N 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 239000000741 silica gel Substances 0.000 description 2
- 229910002027 silica gel Inorganic materials 0.000 description 2
- RXCOGDYOZQGGMK-UHFFFAOYSA-N (3,4-diaminophenyl)-phenylmethanone Chemical compound C1=C(N)C(N)=CC=C1C(=O)C1=CC=CC=C1 RXCOGDYOZQGGMK-UHFFFAOYSA-N 0.000 description 1
- PXPXXPJORACKKN-UHFFFAOYSA-N (5,6-dimethyl-1h-benzimidazol-2-yl)methanethiol Chemical compound C1=C(C)C(C)=CC2=C1NC(CS)=N2 PXPXXPJORACKKN-UHFFFAOYSA-N 0.000 description 1
- SPMLMLQATWNZEE-UHFFFAOYSA-N 2-(chloromethyl)-1h-benzimidazole Chemical compound C1=CC=C2NC(CCl)=NC2=C1 SPMLMLQATWNZEE-UHFFFAOYSA-N 0.000 description 1
- AGTHQQZHEBRMJM-UHFFFAOYSA-N 2-(pyridin-2-ylsulfinylmethyl)-1h-benzimidazole Chemical compound N=1C2=CC=CC=C2NC=1CS(=O)C1=CC=CC=N1 AGTHQQZHEBRMJM-UHFFFAOYSA-N 0.000 description 1
- ZIFYQOSFMFKAAA-UHFFFAOYSA-N 2-(pyrimidin-2-ylsulfanylmethyl)-1h-benzimidazole Chemical compound N=1C2=CC=CC=C2NC=1CSC1=NC=CC=N1 ZIFYQOSFMFKAAA-UHFFFAOYSA-N 0.000 description 1
- MIXQEEBXMVSDLK-UHFFFAOYSA-N 2-[(4-methylpyridin-2-yl)sulfanylmethyl]-1h-benzimidazole Chemical compound CC1=CC=NC(SCC=2NC3=CC=CC=C3N=2)=C1 MIXQEEBXMVSDLK-UHFFFAOYSA-N 0.000 description 1
- WLKHNMXFZOJXJN-UHFFFAOYSA-N 2-[2-[(4-methylpyridin-2-yl)sulfanylmethyl]-3h-benzimidazol-5-yl]acetic acid;hydrochloride Chemical compound Cl.CC1=CC=NC(SCC=2NC3=CC(CC(O)=O)=CC=C3N=2)=C1 WLKHNMXFZOJXJN-UHFFFAOYSA-N 0.000 description 1
- IGJFLPNTKLFHMW-UHFFFAOYSA-N 2-pyridin-2-ylsulfanylacetic acid Chemical compound OC(=O)CSC1=CC=CC=N1 IGJFLPNTKLFHMW-UHFFFAOYSA-N 0.000 description 1
- XVMSFILGAMDHEY-UHFFFAOYSA-N 6-(4-aminophenyl)sulfonylpyridin-3-amine Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=C(N)C=N1 XVMSFILGAMDHEY-UHFFFAOYSA-N 0.000 description 1
- ADEJKVPVKYWIKJ-UHFFFAOYSA-N 6-nitro-2-(pyridin-2-ylsulfinylmethyl)-1h-benzimidazole Chemical compound N1C2=CC([N+](=O)[O-])=CC=C2N=C1CS(=O)C1=CC=CC=N1 ADEJKVPVKYWIKJ-UHFFFAOYSA-N 0.000 description 1
- 206010002091 Anaesthesia Diseases 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 241000347881 Kadua laxiflora Species 0.000 description 1
- 241000699670 Mus sp. Species 0.000 description 1
- 150000001204 N-oxides Chemical class 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 241000700157 Rattus norvegicus Species 0.000 description 1
- TZWARUAGLACBEW-UHFFFAOYSA-N [3-methyl-2-(pyridin-2-ylsulfinylmethyl)benzimidazol-5-yl]-phenylmethanone Chemical compound N=1C2=CC=C(C(=O)C=3C=CC=CC=3)C=C2N(C)C=1CS(=O)C1=CC=CC=N1 TZWARUAGLACBEW-UHFFFAOYSA-N 0.000 description 1
- 230000007059 acute toxicity Effects 0.000 description 1
- 231100000403 acute toxicity Toxicity 0.000 description 1
- 230000037005 anaesthesia Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229940125904 compound 1 Drugs 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- 239000012154 double-distilled water Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- PVGYQKSMWHYJIQ-UHFFFAOYSA-N ethyl 2-(4-methylpyridin-2-yl)sulfanylacetate Chemical compound CCOC(=O)CSC1=CC(C)=CC=N1 PVGYQKSMWHYJIQ-UHFFFAOYSA-N 0.000 description 1
- RIFGWPKJUGCATF-UHFFFAOYSA-N ethyl chloroformate Chemical compound CCOC(Cl)=O RIFGWPKJUGCATF-UHFFFAOYSA-N 0.000 description 1
- 238000001640 fractional crystallisation Methods 0.000 description 1
- 230000027119 gastric acid secretion Effects 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000002350 laparotomy Methods 0.000 description 1
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 239000004540 pour-on Substances 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 210000001187 pylorus Anatomy 0.000 description 1
- HBCQSNAFLVXVAY-UHFFFAOYSA-N pyrimidine-2-thiol Chemical compound SC1=NC=CC=N1 HBCQSNAFLVXVAY-UHFFFAOYSA-N 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
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
- C07D401/12—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 linked by a chain containing hetero atoms as chain links
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Heat Sensitive Colour Forming Recording (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8600695A FR2593178B1 (fr) | 1986-01-20 | 1986-01-20 | Derives de 2-benzimidazolylalkylthio (ou sulfinyle ou sulfonyle) leur preparation et leur application en tant que medicaments. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU1586513A3 true SU1586513A3 (ru) | 1990-08-15 |
Family
ID=9331254
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU874028881A SU1586513A3 (ru) | 1986-01-20 | 1987-01-19 | Способ получени производных 2-алкилбензимидазола |
Country Status (22)
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DK8600939A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1985-03-05 | 1986-09-06 | ||
| SE8804628D0 (sv) * | 1988-12-22 | 1988-12-22 | Ab Haessle | New compounds |
| US6245913B1 (en) | 1999-06-30 | 2001-06-12 | Wockhardt Europe Limited | Synthetic procedure for 5-methoxy-2-[(4-methoxy-3,5-dimethyl-2-pyridinyl)-methylthio]-IH-benzimidazole hydrochloride and its conversion to omeprazole |
| ES2171116B1 (es) * | 2000-04-14 | 2003-08-01 | Esteve Quimica Sa | Procedimiento para la obtencion de derivados de (((piridil sustituido)metil)tio)bencimidazol. |
| GB0108592D0 (en) * | 2001-04-05 | 2001-05-23 | Merck Sharp & Dohme | Therapeutic agents |
| EP2420500A4 (en) * | 2009-04-09 | 2012-09-05 | Arigen Pharmaceuticals Inc | PYRIDINTHIODERIVATE AND PHARMACEUTICAL COMPOSITION THEREOF AND WITH ANTI-HELIDOBACTER PYLORI EFFECT |
| US9708272B2 (en) | 2014-08-29 | 2017-07-18 | Tes Pharma S.R.L. | Inhibitors of α-amino-β-carboxymuconic acid semialdehyde decarboxylase |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1234058A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1968-10-21 | 1971-06-03 | ||
| SE418966B (sv) * | 1974-02-18 | 1981-07-06 | Haessle Ab | Analogiforfarande for framstellning av foreningar med magsyrasekretionsinhiberande verkan |
| US4045564A (en) * | 1974-02-18 | 1977-08-30 | Ab Hassle | Benzimidazole derivatives useful as gastric acid secretion inhibitors |
| US4619944A (en) * | 1981-06-01 | 1986-10-28 | Usv Pharmaceutical Corporation | Antihypertensive compounds |
-
1986
- 1986-01-20 FR FR8600695A patent/FR2593178B1/fr not_active Expired
-
1987
- 1987-01-15 US US07/003,442 patent/US4791114A/en not_active Expired - Fee Related
- 1987-01-16 AU AU67621/87A patent/AU587680B2/en not_active Ceased
- 1987-01-16 DK DK023887A patent/DK23887A/da not_active Application Discontinuation
- 1987-01-16 BR BR8700191A patent/BR8700191A/pt not_active Application Discontinuation
- 1987-01-19 SU SU874028881A patent/SU1586513A3/ru active
- 1987-01-19 AT AT87400112T patent/ATE80625T1/de not_active IP Right Cessation
- 1987-01-19 DE DE8787400112T patent/DE3781703T2/de not_active Expired - Fee Related
- 1987-01-19 YU YU6087A patent/YU45932B/sh unknown
- 1987-01-19 PT PT84141A patent/PT84141B/pt not_active IP Right Cessation
- 1987-01-19 HU HU87137A patent/HU197566B/hu not_active IP Right Cessation
- 1987-01-19 EP EP87400112A patent/EP0234980B1/fr not_active Expired - Lifetime
- 1987-01-19 DE DE198787400112T patent/DE234980T1/de active Pending
- 1987-01-19 DD DD87299334A patent/DD259401A5/de unknown
- 1987-01-19 ES ES8700108A patent/ES2003658A6/es not_active Expired
- 1987-01-19 ZA ZA870343A patent/ZA87343B/xx unknown
- 1987-01-19 CA CA000527612A patent/CA1296336C/fr not_active Expired - Lifetime
- 1987-01-20 KR KR1019870000517A patent/KR890002291B1/ko not_active Expired
- 1987-01-20 PL PL1987263733A patent/PL154487B1/pl unknown
- 1987-01-20 CN CN87100363A patent/CN1016060B/zh not_active Expired
- 1987-01-20 JP JP62011195A patent/JPS62181274A/ja active Pending
- 1987-01-20 NO NO870228A patent/NO170931C/no unknown
-
1988
- 1988-12-16 GR GR88300076T patent/GR880300076T1/el unknown
-
1992
- 1992-10-29 GR GR920402430T patent/GR3006109T3/el unknown
Non-Patent Citations (1)
| Title |
|---|
| Вейганд-Хильгетаг. Методы эксперимента в органической химии. М.: Хими , 1968, с. 598. * |
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