DK141483B - Analogifremgangsmåde til fremstilling af as-triazino-(6,5-c)quinolinderivater. - Google Patents
Analogifremgangsmåde til fremstilling af as-triazino-(6,5-c)quinolinderivater. Download PDFInfo
- Publication number
- DK141483B DK141483B DK247173AA DK247173A DK141483B DK 141483 B DK141483 B DK 141483B DK 247173A A DK247173A A DK 247173AA DK 247173 A DK247173 A DK 247173A DK 141483 B DK141483 B DK 141483B
- Authority
- DK
- Denmark
- Prior art keywords
- triazino
- quinoline
- nitroquinoline
- dihydro
- preparation
- Prior art date
Links
- 238000000034 method Methods 0.000 title description 5
- 238000002360 preparation method Methods 0.000 title description 2
- 229940027991 antiseptic and disinfectant quinoline derivative Drugs 0.000 title 1
- 125000002943 quinolinyl group Chemical class N1=C(C=CC2=CC=CC=C12)* 0.000 title 1
- ARFYZKAYDRJATN-UHFFFAOYSA-N [1,2,4]triazino[5,6-c]quinoline Chemical class C1=NN=C2C3=CC=CC=C3N=CC2=N1 ARFYZKAYDRJATN-UHFFFAOYSA-N 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- -1 hydrazino compound Chemical class 0.000 description 5
- SKRZKNWOHLTARM-UHFFFAOYSA-N (3-nitroquinolin-4-yl)hydrazine Chemical compound C1=CC=C2C(NN)=C([N+]([O-])=O)C=NC2=C1 SKRZKNWOHLTARM-UHFFFAOYSA-N 0.000 description 4
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 4
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- CGIGDMFJXJATDK-UHFFFAOYSA-N indomethacin Chemical compound CC1=C(CC(O)=O)C2=CC(OC)=CC=C2N1C(=O)C1=CC=C(Cl)C=C1 CGIGDMFJXJATDK-UHFFFAOYSA-N 0.000 description 4
- 230000003647 oxidation Effects 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- 230000003110 anti-inflammatory effect Effects 0.000 description 3
- 235000019441 ethanol Nutrition 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- BSYNRYMUTXBXSQ-UHFFFAOYSA-N Aspirin Chemical compound CC(=O)OC1=CC=CC=C1C(O)=O BSYNRYMUTXBXSQ-UHFFFAOYSA-N 0.000 description 2
- YIEHFGMYLXAXMX-UHFFFAOYSA-N N(N)C=1C(=NC2=CC=CC=C2C1)[N+](=O)[O-] Chemical compound N(N)C=1C(=NC2=CC=CC=C2C1)[N+](=O)[O-] YIEHFGMYLXAXMX-UHFFFAOYSA-N 0.000 description 2
- 206010030113 Oedema Diseases 0.000 description 2
- 229960001138 acetylsalicylic acid Drugs 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 125000005907 alkyl ester group Chemical group 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 230000000845 anti-microbial effect Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 229960000905 indomethacin Drugs 0.000 description 2
- 229910052763 palladium Inorganic materials 0.000 description 2
- 229960002895 phenylbutazone Drugs 0.000 description 2
- VYMDGNCVAMGZFE-UHFFFAOYSA-N phenylbutazonum Chemical compound O=C1C(CCCC)C(=O)N(C=2C=CC=CC=2)N1C1=CC=CC=C1 VYMDGNCVAMGZFE-UHFFFAOYSA-N 0.000 description 2
- 238000006722 reduction reaction Methods 0.000 description 2
- 238000007363 ring formation reaction Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 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
- 230000001988 toxicity Effects 0.000 description 2
- 231100000419 toxicity Toxicity 0.000 description 2
- DERASAFMHXNKGC-UHFFFAOYSA-N (3-nitroquinolin-2-yl)hydrazine Chemical compound C1=CC=C2C=C([N+]([O-])=O)C(NN)=NC2=C1 DERASAFMHXNKGC-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 241000699670 Mus sp. Species 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 241000700159 Rattus Species 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 230000000202 analgesic effect Effects 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- OAKJQQAXSVQMHS-UHFFFAOYSA-N hydrazine Substances NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 1
- 125000000717 hydrazino group Chemical group [H]N([*])N([H])[H] 0.000 description 1
- 150000002431 hydrogen Chemical group 0.000 description 1
- PSXRWZBTVAZNSF-UHFFFAOYSA-N hydron;quinoline;chloride Chemical compound Cl.N1=CC=CC2=CC=CC=C21 PSXRWZBTVAZNSF-UHFFFAOYSA-N 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 230000002757 inflammatory effect Effects 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 238000003402 intramolecular cyclocondensation reaction Methods 0.000 description 1
- UETZVSHORCDDTH-UHFFFAOYSA-N iron(2+);hexacyanide Chemical compound [Fe+2].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] UETZVSHORCDDTH-UHFFFAOYSA-N 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
- 229920000053 polysorbate 80 Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000006476 reductive cyclization reaction Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- AWDBHOZBRXWRKS-UHFFFAOYSA-N tetrapotassium;iron(6+);hexacyanide Chemical compound [K+].[K+].[K+].[K+].[Fe+6].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] AWDBHOZBRXWRKS-UHFFFAOYSA-N 0.000 description 1
- GKASDNZWUGIAMG-UHFFFAOYSA-N triethyl orthoformate Chemical compound CCOC(OCC)OCC GKASDNZWUGIAMG-UHFFFAOYSA-N 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen 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
- C07D215/38—Nitrogen atoms
- C07D215/42—Nitrogen atoms attached in position 4
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pain & Pain Management (AREA)
- Public Health (AREA)
- Rheumatology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Quinoline Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HUEE002021 | 1972-05-05 | ||
| HUEE2021A HU165677B (xx) | 1972-05-05 | 1972-05-05 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DK141483B true DK141483B (da) | 1980-03-24 |
| DK141483C DK141483C (xx) | 1980-09-22 |
Family
ID=10995439
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DK247173AA DK141483B (da) | 1972-05-05 | 1973-05-04 | Analogifremgangsmåde til fremstilling af as-triazino-(6,5-c)quinolinderivater. |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US3873541A (xx) |
| JP (1) | JPS563872B2 (xx) |
| AT (1) | AT323749B (xx) |
| CA (1) | CA978188A (xx) |
| CH (1) | CH580627A5 (xx) |
| CS (1) | CS174879B2 (xx) |
| DD (1) | DD106844A5 (xx) |
| DE (1) | DE2322394A1 (xx) |
| DK (1) | DK141483B (xx) |
| FR (1) | FR2183801B1 (xx) |
| GB (1) | GB1382781A (xx) |
| HU (1) | HU165677B (xx) |
| NL (1) | NL7306160A (xx) |
| PL (1) | PL85376B1 (xx) |
| SE (1) | SE403615B (xx) |
| YU (1) | YU36701B (xx) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| HU181689B (en) * | 1980-04-18 | 1983-11-28 | Egyt Gyogyszervegyeszeti Gyar | Process for producing new dihydro-as-triazino-square bracket-5,6-c-square bracket closed-quinoline derivatives |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3597427A (en) * | 1969-01-13 | 1971-08-03 | American Cyanamid Co | 1,2-dihydropyrido(3,4-e)-as-triazines |
| US3721670A (en) * | 1971-04-05 | 1973-03-20 | Morton Norwich Products Inc | 3-substituted-as-triazino(5,6-c)quinolines |
| HU164031B (xx) * | 1971-08-02 | 1973-12-28 |
-
1972
- 1972-05-05 HU HUEE2021A patent/HU165677B/hu not_active IP Right Cessation
-
1973
- 1973-04-30 CH CH617873A patent/CH580627A5/xx not_active IP Right Cessation
- 1973-05-01 US US356174A patent/US3873541A/en not_active Expired - Lifetime
- 1973-05-03 NL NL7306160A patent/NL7306160A/xx not_active Application Discontinuation
- 1973-05-04 DE DE2322394A patent/DE2322394A1/de active Pending
- 1973-05-04 DK DK247173AA patent/DK141483B/da unknown
- 1973-05-04 CS CS3184A patent/CS174879B2/cs unknown
- 1973-05-04 CA CA170,469A patent/CA978188A/en not_active Expired
- 1973-05-04 YU YU1192/73A patent/YU36701B/xx unknown
- 1973-05-04 AT AT394373A patent/AT323749B/de not_active IP Right Cessation
- 1973-05-04 GB GB2125373A patent/GB1382781A/en not_active Expired
- 1973-05-04 FR FR7316126A patent/FR2183801B1/fr not_active Expired
- 1973-05-04 DD DD170617A patent/DD106844A5/xx unknown
- 1973-05-04 JP JP5022973A patent/JPS563872B2/ja not_active Expired
- 1973-05-04 PL PL1973162336D patent/PL85376B1/pl unknown
- 1973-05-04 SE SE7306317A patent/SE403615B/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| JPS4947396A (xx) | 1974-05-08 |
| CS174879B2 (xx) | 1977-04-29 |
| AT323749B (de) | 1975-07-25 |
| DE2322394A1 (de) | 1973-11-15 |
| FR2183801B1 (xx) | 1976-05-14 |
| CA978188A (en) | 1975-11-18 |
| NL7306160A (xx) | 1973-11-07 |
| HU165677B (xx) | 1974-10-28 |
| YU119273A (en) | 1982-02-25 |
| SE403615B (sv) | 1978-08-28 |
| US3873541A (en) | 1975-03-25 |
| JPS563872B2 (xx) | 1981-01-27 |
| DD106844A5 (xx) | 1974-07-05 |
| PL85376B1 (en) | 1976-04-30 |
| DK141483C (xx) | 1980-09-22 |
| CH580627A5 (xx) | 1976-10-15 |
| GB1382781A (en) | 1975-02-05 |
| FR2183801A1 (xx) | 1973-12-21 |
| YU36701B (en) | 1984-08-31 |
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