UST100505I4 - Triazolo[4,3-a]pyridin-3(2H)-ones - Google Patents
Triazolo[4,3-a]pyridin-3(2H)-ones Download PDFInfo
- Publication number
- UST100505I4 UST100505I4 US06/130,900 US13090080A UST100505I4 US T100505 I4 UST100505 I4 US T100505I4 US 13090080 A US13090080 A US 13090080A US T100505 I4 UST100505 I4 US T100505I4
- Authority
- US
- United States
- Prior art keywords
- triazolo
- och
- compounds
- pyridin
- divalent
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 101150108015 STR6 gene Proteins 0.000 abstract 1
- 101100386054 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) CYS3 gene Proteins 0.000 abstract 1
- 230000000202 analgesic effect Effects 0.000 abstract 1
- 230000000049 anti-anxiety effect Effects 0.000 abstract 1
- 230000001430 anti-depressive effect Effects 0.000 abstract 1
- 230000000561 anti-psychotic effect Effects 0.000 abstract 1
- 239000000935 antidepressant agent Substances 0.000 abstract 1
- 229940005513 antidepressants Drugs 0.000 abstract 1
- 239000002249 anxiolytic agent Substances 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 210000003169 central nervous system Anatomy 0.000 abstract 1
- 238000009533 lab test Methods 0.000 abstract 1
- 230000000144 pharmacologic effect Effects 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 125000004193 piperazinyl group Chemical group 0.000 abstract 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 1
- 101150035983 str1 gene Proteins 0.000 abstract 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Triazolo[4,3-a]pyridin-3-(2H)-one derivatives containing a 4-(optionally substituted phenyl)piperazinyl component attached to the two position of the triazolo-[4,3-a]pyridine component via a divalent radical such as --(CH2)5 --, --(CH2)6 --, --CH3 CH(CH3)CH2 --, --CH2 C(CH3)2 CH2 --, --CH2 CH═CHCH2 --, --CH2 C.tbd.CCH2 --, --CH2 CH2 OCH2 CH2 -- or a divalent cycloalkylene radical of 3 to 6 carbon atoms are disclosed. The compounds are useful in that they exhibit central nervous system pharmacological properties in standard laboratory tests considered predictive of analgetics, anti-psychotic (neuroleptics), antidepressant and antianxiety utility. Examples of specific embodiments of the invention are compounds having the formula
______________________________________
##STR1##
Y R
______________________________________
##STR2## 3-Cl
##STR3## H
##STR4## 3-Cl
##STR5## 3-CF3
##STR6## 4-F
CH2 CHCHCH2
3-Cl
CH2 CCCH2
3-Cl
(CH2)5 3-Cl
(CH2)5 4-CH3 O
(CH2)5 2-CH3
(CH2)6 3-Cl
CH2 C(CH3)2 CH2
3-Cl
CH2 CH(CH3)CH2
3-CF3
CH2 CH2 OCH2 CH2
3-Cl
______________________________________
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/130,900 UST100505I4 (en) | 1980-03-17 | 1980-03-17 | Triazolo[4,3-a]pyridin-3(2H)-ones |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/130,900 UST100505I4 (en) | 1980-03-17 | 1980-03-17 | Triazolo[4,3-a]pyridin-3(2H)-ones |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| UST100505I4 true UST100505I4 (en) | 1981-04-07 |
Family
ID=22446883
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US06/130,900 Pending UST100505I4 (en) | 1980-03-17 | 1980-03-17 | Triazolo[4,3-a]pyridin-3(2H)-ones |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | UST100505I4 (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4402956A (en) | 1980-04-09 | 1983-09-06 | Aziende Chimiche Riunite Angelini Francesco Acraf Spa | 2-[3-[4-(3-Chloro-4-fluorophenyl)-1-piperazinyl]propyl]-1,2,4-triazolo[4,3-a]pyridin-3(2H)-one |
| US5622951A (en) * | 1993-01-06 | 1997-04-22 | John Wyeth & Brother Ltd. | Piperazine derivatives as 5-HT antagonists |
| US5726178A (en) * | 1992-01-17 | 1998-03-10 | Istituto Ricerca Francesco Angelini S.P.A. | Alkyl derivatives of trazodone with CNS activity |
-
1980
- 1980-03-17 US US06/130,900 patent/UST100505I4/en active Pending
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4402956A (en) | 1980-04-09 | 1983-09-06 | Aziende Chimiche Riunite Angelini Francesco Acraf Spa | 2-[3-[4-(3-Chloro-4-fluorophenyl)-1-piperazinyl]propyl]-1,2,4-triazolo[4,3-a]pyridin-3(2H)-one |
| US5726178A (en) * | 1992-01-17 | 1998-03-10 | Istituto Ricerca Francesco Angelini S.P.A. | Alkyl derivatives of trazodone with CNS activity |
| US5739334A (en) * | 1992-01-17 | 1998-04-14 | Istituto Ricerca Francesco Angelini S.P.A. | Alkyl derivatives of trazodone with CNS activity |
| US5622951A (en) * | 1993-01-06 | 1997-04-22 | John Wyeth & Brother Ltd. | Piperazine derivatives as 5-HT antagonists |
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