IL58237A0 - Substituted bis-benzimidazolyl compounds process for their manufacture and their use in treating protozoal virus diseases - Google Patents
Substituted bis-benzimidazolyl compounds process for their manufacture and their use in treating protozoal virus diseasesInfo
- Publication number
- IL58237A0 IL58237A0 IL58237A IL5823779A IL58237A0 IL 58237 A0 IL58237 A0 IL 58237A0 IL 58237 A IL58237 A IL 58237A IL 5823779 A IL5823779 A IL 5823779A IL 58237 A0 IL58237 A0 IL 58237A0
- Authority
- IL
- Israel
- Prior art keywords
- atoms
- formula
- denotes
- see diagramm
- alkyl
- Prior art date
Links
- 238000004519 manufacturing process Methods 0.000 title abstract 2
- 238000000034 method Methods 0.000 title abstract 2
- 241000700605 Viruses Species 0.000 title 1
- 201000010099 disease Diseases 0.000 title 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title 1
- -1 2,5-thiophenediyl Chemical group 0.000 abstract 8
- 125000000217 alkyl group Chemical group 0.000 abstract 7
- 125000004432 carbon atom Chemical group C* 0.000 abstract 7
- 150000001875 compounds Chemical class 0.000 abstract 5
- 150000003839 salts Chemical class 0.000 abstract 4
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 abstract 2
- 125000004103 aminoalkyl group Chemical group 0.000 abstract 2
- 125000004429 atom Chemical group 0.000 abstract 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 125000005448 ethoxyethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])C([H])([H])* 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 2
- 125000006203 morpholinoethyl group Chemical group [H]C([H])(*)C([H])([H])N1C([H])([H])C([H])([H])OC([H])([H])C1([H])[H] 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/18—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
- C07D295/195—Radicals derived from nitrogen analogues of carboxylic acids
-
- 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
- A61P31/12—Antivirals
-
- 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
- C07D235/20—Two benzimidazolyl-2 radicals linked together directly or via a hydrocarbon or substituted hydrocarbon radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/56—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
- C07D307/68—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom 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
- C07D333/38—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Communicable Diseases (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Virology (AREA)
- Oncology (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)
Abstract
(For Contracting States : BE, CH, DE, FR, GB, IT, NL) 1. Substituted bis-benzimidazolyl compounds of the general formula I see diagramm : EP0009163,P13,F1 and their physiologically compatible salts, in which A denotes 2,5-thiophenediyl, 2,5-furanediyl, p-phenylene, m-phenylene or 4,4'-phenoxyphenylene, and in which R**1 is represented by one of the general formulae IIa or IIb see diagramm : EP0009163,P14,F2 in which the radicals R**2 to R**4 independently of one another denote hydrogen, alkyl with 1-18 C atoms, cycloalkyl with 5-8 atoms, aminoalkyl, N-alkylaminoalkyl or N,N-dialkylaminoalkyl, in which an alkyl group in each case has 1-4 C atoms, morpholinoethyl, methoxyethyl, ethoxyethyl, benzyl, phenethyl or phenyl, or in which the radicals R**2 and R**3 together denote an alkylene bridge with 4, 5 or 6 CH2 groups, and in which Y denotes O, S, NH or N-R**5, in which R**5 represents alkyl with 1-4 C atoms. (For Contracting State AT) 1. Process for the manufacture of substituted bis-benzimidazolyl compounds of the general formula I see diagramm : EP0009163,P15,F1 and their physiologically compatible salts, in which A denotes 2,5-thiophenediyl, 2,5-furanediyl, p-phenylene, m-phenylene or 4,4'-phenoxyphenylene, and in which R**1 is represented by one of the general formulae IIa or IIb see diagramm : EP0009163,P15,F2 in which the radicals R**2 to R**4 independently of one another denote hydrogen, alkyl with 1-18 C atoms, cycloalkyl with 5-8 atoms, aminoalkyl, N-alkylaminoalkyl or N,N-dialkylaminoalkyl, in which an alkyl group in each case has 1-4 C atoms, morpholinoethyl, methoxyethyl, ethoxyethyl, benzyl, phenethyl or phenyl, or in which the radicals R**2 and R**3 together denote an alkylene bridge with 4, 5 or 6 CH2 groups, and in which Y denotes O, S, NH or N-R**5, in which R**5 represents alkyl with 1-4 C atoms, which comprises a) reacting a compound of the formula III R**6-A-R**6 in which A has the meanings indicated above and in which R**6 denotes see diagramm : EP0009163,P15,F3 in which Z denotes O or S and R**7 denotes alkyl or alkoxyalkyl with, in each case, 1 to 4 C atoms per alkyl radical, with a compound of the formula IV see diagramm : EP0009163,P15,F4 in which R**1 has the meanings indicated by the formula IIa or IIb, or b) reacting a compound of the general formula V see diagramm : EP0009163,P15,F5 in which A has the meanings indicated above and in which R**6 has the meanings indicated under a) under formula III, with an amine of the formula VIa or VIb see diagramm : EP0009163,P15,F6 in which R**2, R**3 and Y have the meanings indicated under formula IIa or IIb, and optionally converting a compound of the formula I, which is thus obtained, into its salt by adding a physiologically compatible acid HX, or converting a salt of the formula I, which is thus obtained, into a compound of the formula I by adding a base.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19782839989 DE2839989A1 (en) | 1978-09-14 | 1978-09-14 | SUBSTITUTED BISBENZIMIDAZOLYL COMPOUNDS, THEIR PRODUCTION AND THEIR USE |
Publications (1)
Publication Number | Publication Date |
---|---|
IL58237A0 true IL58237A0 (en) | 1979-12-30 |
Family
ID=6049430
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
IL58237A IL58237A0 (en) | 1978-09-14 | 1979-09-12 | Substituted bis-benzimidazolyl compounds process for their manufacture and their use in treating protozoal virus diseases |
Country Status (8)
Country | Link |
---|---|
EP (1) | EP0009163B1 (en) |
JP (1) | JPS5540689A (en) |
AT (1) | ATE1285T1 (en) |
AU (1) | AU5082779A (en) |
DE (2) | DE2839989A1 (en) |
ES (2) | ES483994A1 (en) |
IL (1) | IL58237A0 (en) |
ZA (1) | ZA794864B (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
USD976707S1 (en) * | 2020-09-30 | 2023-01-31 | Guangdong Industry Polytechnic | Bottle |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5667975A (en) * | 1994-05-06 | 1997-09-16 | The University Of North Carolina | Method of fluorescent detection of nucleic acids and cytoskeleton elements using bis-dicationic aryl furans |
US5643935A (en) * | 1995-06-07 | 1997-07-01 | The University Of North Carolina At Chapel Hill | Method of combatting infectious diseases using dicationic bis-benzimidazoles |
US5935982A (en) * | 1997-02-28 | 1999-08-10 | The University Of North Carolina At Chapel Hill | Methods of treating retroviral infection and compounds useful therefor |
WO1999026933A1 (en) * | 1997-11-26 | 1999-06-03 | Axys Pharmaceuticals, Inc. | Substituted amidinoaryl derivatives and their use as anticoagulants |
WO1999026932A1 (en) * | 1997-11-26 | 1999-06-03 | Axys Pharmaceuticals, Inc. | By amidino group substituted heterocyclic derivatives and their use as anticoagulants |
US20070088067A1 (en) * | 2003-09-05 | 2007-04-19 | Tidwell Richards R | Novel amidine compounds for treating microbial infections |
AU2006282428A1 (en) * | 2005-08-23 | 2007-03-01 | Ube Industries, Ltd. | Method for producing 1-substituted-5-acylimidazole compound |
EP3710442A2 (en) | 2017-11-17 | 2020-09-23 | The Scripps Research Institute | Bis-benzimidazole compounds and methods of using the same |
CN109369612A (en) * | 2018-12-17 | 2019-02-22 | 桂林理工大学 | A kind of aryl radical precursor molecule with symmetrical structure and preparation method thereof |
CN109651370A (en) * | 2018-12-17 | 2019-04-19 | 桂林理工大学 | A kind of purine analog derivative free radical precursor molecule and preparation method thereof |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL268089A (en) * | 1960-08-11 | |||
DE1645944A1 (en) * | 1965-12-06 | 1971-05-13 | Dynachim Sarl | Fungicide |
DE2711362A1 (en) * | 1977-03-16 | 1978-09-21 | Hoechst Ag | Bis-benzimidazole derivs. - useful as antiparasitic and antiviral agents |
-
1978
- 1978-09-14 DE DE19782839989 patent/DE2839989A1/en not_active Withdrawn
-
1979
- 1979-09-04 AT AT79103260T patent/ATE1285T1/en active
- 1979-09-04 DE DE7979103260T patent/DE2963244D1/en not_active Expired
- 1979-09-04 EP EP79103260A patent/EP0009163B1/en not_active Expired
- 1979-09-07 ES ES483994A patent/ES483994A1/en not_active Expired
- 1979-09-07 ES ES483990A patent/ES483990A1/en not_active Expired
- 1979-09-12 IL IL58237A patent/IL58237A0/en unknown
- 1979-09-13 ZA ZA00794864A patent/ZA794864B/en unknown
- 1979-09-13 AU AU50827/79A patent/AU5082779A/en not_active Abandoned
- 1979-09-14 JP JP11744679A patent/JPS5540689A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
USD976707S1 (en) * | 2020-09-30 | 2023-01-31 | Guangdong Industry Polytechnic | Bottle |
Also Published As
Publication number | Publication date |
---|---|
JPS5540689A (en) | 1980-03-22 |
ES483990A1 (en) | 1980-05-16 |
ATE1285T1 (en) | 1982-07-15 |
EP0009163B1 (en) | 1982-06-30 |
DE2839989A1 (en) | 1980-04-03 |
AU5082779A (en) | 1980-03-20 |
ZA794864B (en) | 1980-08-27 |
DE2963244D1 (en) | 1982-08-19 |
EP0009163A2 (en) | 1980-04-02 |
ES483994A1 (en) | 1980-05-16 |
EP0009163A3 (en) | 1980-04-16 |
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