EP0005129B1
Expired / Lapsed
EP
⏱️ 0.0 years remaining
Substituted pyridylsulfinylbenzimidazoles having gastric acid secretion properties, pharmaceutical preparations containing same, and intermediates for their preparation
Assignee: Hassle AB
•
Filing: 1979-04-03
•
Granted: 1981-04-29
•
Expires: 1999-04-03
Abstract
No abstract record available.
Inventors
- 👤 Ulf Krister Junggren
- 👤 Sven Erik Sjöstrand
Bibliographic Details
Application Number
—
Jurisdiction
EP
Data Source
google_patents
Last Synchronized
2026-11-02 21:16
CPC Classifications
C; C07; C07D; C07D401/00; C07D401/02; C07D401/12; A; A61; A61P; A61P1/00; A61P1/04; A61P1/14
Claims Analysis
Total Claims: 6
Claim 1
Independent Claim
114 words
A compound of formula III or a therapeutically acceptable salt thereof in which R I and R 2 are the same or different and are hydrogen, alkyl, halogen, methoxycarbonyl, ethoxycarbonyl, alkoxy, or alkanoyl in any position, R 6 is hydrogen, methyl or ethyl, R 3 , R 4 and R 5 are the same or different and are each hydrogen, methyl, methoxy, ethox), methoxyethoxy or ethoxyethoxy, whereby R 3 , R 4 , and R 5 and R 5 are not all hydrogen, and whereby when two of R 3 , R 4 , and R 5 are hydrogen, the third of R 3 , R 4 , and R 5 is not methyl.
Claim 2
Dependent Claim
114 words
A compound of formula III or a therapeutically acceptable salt thereof in which R I and R 2 are the same or different and are hydrogen, alkyl, halogen, methoxycarbonyl, ethoxycarbonyl, alkoxy, or alkanoyl in any position, R 6 is hydrogen, methyl or ethyl, R 3 , R 4 and R 5 are the same or different and are each hydrogen, methyl, methoxy, ethox), methoxyethoxy or ethoxyethoxy, whereby R 3 , R 4 , and R 5 and R 5 are not all hydrogen, and whereby when two of R 3 , R 4 , and R 5 are hydrogen, the third of R 3 , R 4 , and R 5 is not methyl.
Claim 3
Dependent Claim
34 words
A compound according to claim 1, which is 2-[2-(3,4-dimethyl-pyridyl)methylsulfinyl]-5-acetyl-6-methyl-benzimidazole, 2-[2-(3,5-dimethyl-pyridyl)methylsulfinyl]-4,6-dimethyl-benzimidazole, 2-[2-(4,5-dimethyl-pyridyl)methylsulfinyl]-5-methoxy-carbonyl-benzimidazole, 2-[2-(4,5-dimethyl-pyridyl)methylsulfinyl]-5-acetyl-6-methyl-benzimidazole, 2-[2-(4,5-dimethyl-pyridyl)methylsulfinyl]-5-methoxy-carbonyl-6-methyl-benzimidazole, 2-[2-(3,4-dimethyl-pyridyl)methylsulfinyl]-5-methoxy-carbonyl-6-methyl-benzimidazole, 2-[2-(3,5-dimethyl-pyridyl)methylsulfinyl]-5-acetyl-6-methyl-benzimidazole, 2-[2-(3,4,5-trimethyl-pyridyl)methylsulfinyl]-5-acetyl-6-methyl-benzimidazole, 2-[2-(4-methoxy-pyridyl)methylsulfinyl]-5-acetyl-6-methyl-benzimidazole, 2-[2-(4-methoxy-pyridyl)methylsulfinyl]-4,6-dimethyl-benzimidazole, 2-[2-(3,5-dimethyl-4-methoxy-pyridyl)methylsulfinyl]-5-acetyl-6-methyl-benzimidazole, 2-[2-(3,5-dimethyl-pyridyl)methylsulfinyl]-5-methoxy-carbonyl-6-methyl-benzimidazole, 2-[2-(3,4,5-trimethyl-pyridyl)methylsulfinyl-5-methoxy-carbonyl-6-methyl-benzimidazole, 2-[2-(4-methoxy-pyridyl)methylsulfinyl]-5-methoxycarbonyl-6-methyl-benzimidazole, 2-[2-(4-ethoxy-pyridyl)methylsulfinyl]-5-methoxycarbonyl-6-methyl-benzimidazole, 2-[2-(3-methyl-4-methoxy-pyridyl)methylsulfinyl]-5-methoxycarbonyl-6-methyl-benzimidazole, 2-[2-(3,5-dimethyl-4-methoxy-pyridyl)methylsulfinyl]-5-methoxycarbonyl-6-methylbenzimidazole, 2-[2-(4-methoxy-5-methyl-pyridyl)methylsufinyl]-5-methoxycarbonyl-6-methyl-benzimidazole, 2-[2-(3,5-dimethyl-pyridyl)methylsulfinyl]-5-methoxycarbonyl-benzimidazole, 2-[2-(3,5-dimethyl-4-methoxy-pyridyl)methylsulfinyl]-5-methoxycarbonyl-benzimidazole, 2-[2-(3,5-dimethyl-4-methoxy-pyridyl)methylsulfinyl]-5-acetyl-benzimidazole, 2-[2-(4-methoxy-5-methyl-pyridyl)methylsulfinyl]-5-methoxy-benzimidazole, 2-[2-(3,5-dimethyl-4-methoxy-pyridyl)methylsulfinyl]-5-methoxy-benzimidazole, 2-[2-(3,5-dimethyl-4-methoxy-pyridyl)methy)sulfinyl]-5-methy)-benzimidazole, 2-[2-(3,5-dimethyl-4-methoxy-pyridyl)methylsulfinyl]-benzimidazole, 2-[2-(3,5-dimethyl-4-methoxy-pyridyl)methylsulfinyl]-5-chloro-benzimidazole
Claim 4
Dependent Claim
43 words
A pharmaceutical preparation for inhibiting gastric acid secretion, characterized in that it contains as active agent a compound according to claim 1 or a pharmaceutically acceptable non-toxic acid addition salt thereof in a therapeutically effective amount in combination with a pharmaceutically acceptable carrier.
Claim 5
Dependent Claim
20 words
A pharmaceutical preparation according to claim 3 wherein the active ingredient is one of the compounds according to claim 2.
Claim 6
Dependent Claim
28 words
Intermediates of the formula wherein R I , R 2 , R 3 , R 4 , R 5 and R 6 are defined according to claim 1.
References Cited (Backward Citations)
No citation records indexed.
USPTO Annuity & Maintenance Windows
Maintenance schedule is calculated for granted US utility patents.