PH20465A - Substituted 6 aryl 1,2,4 triazolo 4,3-b pyridazines - Google Patents
Substituted 6 aryl 1,2,4 triazolo 4,3-b pyridazinesInfo
- Publication number
- PH20465A PH20465A PH30469A PH30469A PH20465A PH 20465 A PH20465 A PH 20465A PH 30469 A PH30469 A PH 30469A PH 30469 A PH30469 A PH 30469A PH 20465 A PH20465 A PH 20465A
- Authority
- PH
- Philippines
- Prior art keywords
- carbon atoms
- formula
- chlorine
- alkyl
- phenyl
- Prior art date
Links
- -1 3-b pyridazines Chemical class 0.000 title abstract 5
- 125000003118 aryl group Chemical group 0.000 title 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 18
- 125000000217 alkyl group Chemical group 0.000 abstract 14
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 10
- 229910052801 chlorine Inorganic materials 0.000 abstract 10
- 239000000460 chlorine Substances 0.000 abstract 10
- 150000001875 compounds Chemical class 0.000 abstract 10
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 10
- 229910052731 fluorine Inorganic materials 0.000 abstract 7
- 239000011737 fluorine Substances 0.000 abstract 7
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 6
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 6
- 229910052794 bromium Inorganic materials 0.000 abstract 6
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 4
- 125000001153 fluoro group Chemical group F* 0.000 abstract 4
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 4
- 150000003839 salts Chemical class 0.000 abstract 4
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 3
- 239000002253 acid Substances 0.000 abstract 3
- 229910052740 iodine Inorganic materials 0.000 abstract 3
- 125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 abstract 2
- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 abstract 2
- 125000000590 4-methylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 abstract 2
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 2
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 abstract 2
- 239000003795 chemical substances by application Substances 0.000 abstract 2
- 238000009833 condensation Methods 0.000 abstract 2
- 230000005494 condensation Effects 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- 125000006254 cycloalkyl carbonyl group Chemical group 0.000 abstract 2
- 125000003884 phenylalkyl group Chemical group 0.000 abstract 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 2
- 150000001412 amines Chemical class 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—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
- A61P25/08—Antiepileptics; Anticonvulsants
-
- 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
- A61P25/20—Hypnotics; Sedatives
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Neurosurgery (AREA)
- Life Sciences & Earth Sciences (AREA)
- Neurology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Biomedical Technology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Anesthesiology (AREA)
- Pain & Pain Management (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Steroid Compounds (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
Abstract
For the Contracting States : BE, CH, DE, FR, GB, IT, LI, LU, NL, SE 1. Compounds of the formula see diagramm : EP0121490,P11,F1 and salts thereof with a physiologically acceptable acid, in which formula R**1 and R**2 are identical or different and represent hydrogen, alkyl groups having 1-6 carbon atoms, phenyl or chlorine, R**3 denotes linear or branched alkyl having 1-6 carbon atoms, cycloalkyl having 3-8 carbon atoms, phenylalkyl which has 1-4 carbon atoms in the alkyl part and is optionally monosubstituted, disubstituted or trisubstituted in the phenyl part by fluorine, chlorine, bromine, iodine, trifluoromethyl or alkyl having 1-4 carbon atoms, alkylcarbonyl having 1-6 carbon atoms in the alkyl part, cycloalkylcarbonyl having 5-7 carbon atoms in the cycloalkyl part, or benzoyl which is optionally monosubstituted, disubstituted or trisubstituted by fluorine, chlorine, bromine, iodine, trifluoromethyl or alkyl having 1-4 carbon atoms, or denotes Ar, and in which Ar represents phenyl, phenoxyphenyl, phenylthiophenyl, 2-thienyl or 2-furyl, these radicals being optionally monosubstituted or disubstituted by fluorine, chlorine, alkyl groups having 1-6 carbon atoms, cyano or trifluoromethyl, with the exception of compounds of the formula I in which R**1 and R**2 denote hydrogen, R**3 denotes phenyl and Ar denotes phenyl or 4-methylphenyl. For the Contracting State AT 1. A process for the preparation of compounds of the formula I see diagramm : EP0121490,P13,F1 and salts thereof with a physiologically acceptable acid, in which formula R**1 and R**2 are identical or different and represent hydrogen, alkyl groups having 1-6 carbon atoms, phenyl or chlorine, R**3 denotes linear or branched alkyl having 1-6 carbon atoms, cycloalkyl having 3-8 carbon atoms, phenylalkyl which has 1-4 carbon atoms in the alkyl part and is optionally monosubstituted, disubstituted or trisubstituted in the phenyl part by fluorine, chlorine, bromine, iodine, trifluoromethyl or alkyl having 1-4 carbon atoms, alkylcarbonyl having 1-6 carbon atoms in the alkyl part, cycloalkylcarbonyl having 5-7 carbon atoms in the cycloalkyl part, or benzoyl which is optionally monosubstituted, disubstituted or trisubstituted by fluorine, chlorine, bromine, iodine, trifluoromethyl or alkyl having 1-4 carbon atoms, or denotes Ar, and in which Ar represents phenyl, phenoxyphenyl, phenylthiophenyl, 2-thienyl or 2-furyl, these radicals being optionally monosubstituted or disubstituted by fluorine, chlorine, alkyl groups having 1-6 carbon atoms, cyano or trifluoromethyl, with the exception of compounds of the formula I in which R**1 and R**2 denote hydrogen, R**3 denotes phenyl and Ar denotes phenyl or 4-methylphenyl, which comprises a) cyclizing a compound of the formula II see diagramm : EP0121490,P13,F2 in which Ar, R**1, R**2 and R**3 have the meanings indicated for formula I and Z represents O or S, by heating, if appropriate with the addition of a condensation agent, to give a compound of the formula I, or b) by reacting a compound of the formula III see diagramm : EP0121490,P13,F3 in which R**6 denotes chlorine, bromine or methylthio and Ar, R**1 and R**2 have the meanings indicated for formula I, with an amine of the formule IV see diagramm : EP0121490,P14,F4 in which R**3 has the meaning indicated for formula I, or c) reacting, if appropriate with the addition of a condensation agent or catalyst, a compound of the formula V see diagramm : EP0121490,P14,F5 or one of its salts in which Ar, R**1 and R**2 have the meanings indicated for formula I, with a compound of the formula VI R**3-Y in which R**3 has the meaning indicated for formula I and Y represents a leaving group, such as, for example, fluorine, chlorine, bromine, iodine, see diagramm : EP0121490,P14,F6 or the tosylate radical, and, if appropriate, converting a compound thus obtained into a salt thereof by adding a physiologically acceptable acid.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19833311753 DE3311753A1 (en) | 1983-03-31 | 1983-03-31 | SUBSTITUTED 6-ARYL-1,2,4-TRIAZOLO (4,3-B) PYRIDAZINE - THEIR PRODUCTION AND USE - |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PH20465A true PH20465A (en) | 1987-01-14 |
Family
ID=6195196
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PH30469A PH20465A (en) | 1983-03-31 | 1984-03-29 | Substituted 6 aryl 1,2,4 triazolo 4,3-b pyridazines |
Country Status (19)
| Country | Link |
|---|---|
| EP (1) | EP0121490B1 (en) |
| JP (1) | JPS59184179A (en) |
| KR (1) | KR840008361A (en) |
| AT (1) | ATE32723T1 (en) |
| AU (1) | AU563556B2 (en) |
| CA (1) | CA1246568A (en) |
| DE (2) | DE3311753A1 (en) |
| DK (1) | DK144884A (en) |
| ES (1) | ES8501765A1 (en) |
| FI (1) | FI841238A7 (en) |
| GR (1) | GR81812B (en) |
| HU (1) | HU189076B (en) |
| IL (1) | IL71412A (en) |
| MA (1) | MA20080A1 (en) |
| NO (1) | NO841270L (en) |
| NZ (1) | NZ207691A (en) |
| PH (1) | PH20465A (en) |
| PT (1) | PT78343B (en) |
| ZA (1) | ZA842389B (en) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4654343A (en) * | 1985-10-31 | 1987-03-31 | American Cyanamid Company | N-substituted-N[3-(1,2,4-triazolo[4,3-b]pyridazin-6-yl)phenyl]alkanamides, carbamates and ureas |
| JP2010500365A (en) | 2006-08-07 | 2010-01-07 | インサイト・コーポレイション | Triazolotriazines as kinase inhibitors |
| JP5572388B2 (en) | 2006-11-22 | 2014-08-13 | インサイト・コーポレイション | Imidazotriazines and imidazopyrimidines as kinase inhibitors |
| JP6022158B2 (en) | 2008-05-21 | 2016-11-09 | インサイト・ホールディングス・コーポレイションIncyte Holdings Corporation | 2-Fluoro-N-methyl-4- [7- (quinolin-6-yl-methyl) -imidazo [1,2-b] [1,2,4] triazin-2-yl] benzamide salt and Methods related to preparing |
| ES2608329T3 (en) | 2010-02-03 | 2017-04-07 | Incyte Holdings Corporation | Imidazo [1,2-b] [1,2,4] triazines as c-Met inhibitors |
| MX2013012661A (en) * | 2011-04-29 | 2014-03-27 | Amgen Inc | Bicyclic pyridazine compounds as pim inhibitors. |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL128809C (en) * | 1966-06-18 | |||
| DE2113438A1 (en) * | 1971-03-19 | 1972-09-21 | Boehringer Mannheim Gmbh | Anti-microbial nitrofuryl-triazolo -(4,3-b) - pyridazine derivs - used for treating urinary system infections |
| US3915968A (en) * | 1973-09-21 | 1975-10-28 | Lepetit Spa | Triazolopyridazines |
| DE3217325A1 (en) * | 1982-05-08 | 1983-11-10 | Hoechst Ag, 6230 Frankfurt | 3-AMINO-6-ARYL-1,2,4-TRIAZOLO (4,3-B) -PYRIDAZINE, THEIR PRODUCTION AND USE |
| DE3222342A1 (en) * | 1982-06-14 | 1983-12-15 | Hoechst Ag, 6230 Frankfurt | 6-Aryl-1,2,4-triazolo[4,3-b]pyridazine-3-carbamates, their preparation and medicaments containing them |
-
1983
- 1983-03-31 DE DE19833311753 patent/DE3311753A1/en not_active Withdrawn
-
1984
- 1984-02-29 DK DK144884A patent/DK144884A/en not_active Application Discontinuation
- 1984-03-26 HU HU841204A patent/HU189076B/en unknown
- 1984-03-28 AT AT84710009T patent/ATE32723T1/en not_active IP Right Cessation
- 1984-03-28 DE DE8484710009T patent/DE3469530D1/en not_active Expired
- 1984-03-28 FI FI841238A patent/FI841238A7/en not_active Application Discontinuation
- 1984-03-28 EP EP84710009A patent/EP0121490B1/en not_active Expired
- 1984-03-29 NZ NZ207691A patent/NZ207691A/en unknown
- 1984-03-29 PH PH30469A patent/PH20465A/en unknown
- 1984-03-29 GR GR74257A patent/GR81812B/el unknown
- 1984-03-29 KR KR1019840001627A patent/KR840008361A/en not_active Withdrawn
- 1984-03-29 ES ES531084A patent/ES8501765A1/en not_active Expired
- 1984-03-30 NO NO841270A patent/NO841270L/en unknown
- 1984-03-30 JP JP59061286A patent/JPS59184179A/en active Pending
- 1984-03-30 IL IL71412A patent/IL71412A/en unknown
- 1984-03-30 ZA ZA842389A patent/ZA842389B/en unknown
- 1984-03-30 PT PT78343A patent/PT78343B/en not_active IP Right Cessation
- 1984-03-30 CA CA000451005A patent/CA1246568A/en not_active Expired
- 1984-03-30 AU AU26346/84A patent/AU563556B2/en not_active Ceased
- 1984-03-31 MA MA20302A patent/MA20080A1/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| DE3469530D1 (en) | 1988-04-07 |
| PT78343A (en) | 1984-04-01 |
| PT78343B (en) | 1986-07-14 |
| EP0121490B1 (en) | 1988-03-02 |
| HUT34193A (en) | 1985-02-28 |
| MA20080A1 (en) | 1984-10-01 |
| AU2634684A (en) | 1984-10-04 |
| AU563556B2 (en) | 1987-07-16 |
| FI841238A7 (en) | 1984-10-01 |
| ES531084A0 (en) | 1984-12-01 |
| DK144884A (en) | 1984-10-01 |
| KR840008361A (en) | 1984-12-14 |
| GR81812B (en) | 1984-12-12 |
| IL71412A0 (en) | 1984-06-29 |
| ES8501765A1 (en) | 1984-12-01 |
| IL71412A (en) | 1988-05-31 |
| DK144884D0 (en) | 1984-02-29 |
| FI841238A0 (en) | 1984-03-28 |
| ATE32723T1 (en) | 1988-03-15 |
| NZ207691A (en) | 1986-07-11 |
| CA1246568A (en) | 1988-12-13 |
| NO841270L (en) | 1984-10-01 |
| EP0121490A1 (en) | 1984-10-10 |
| DE3311753A1 (en) | 1984-10-04 |
| ZA842389B (en) | 1984-11-28 |
| JPS59184179A (en) | 1984-10-19 |
| HU189076B (en) | 1986-06-30 |
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