NI201100133A - DERIVATIVES OF 2-PYRIDIN - 2 - IL - PIRAZOL - 3 (2H) -ONA, ITS PREPARATION AND ITS APPLICATION IN THERAPEUTICS AS HIF ACTIVATORS - Google Patents
DERIVATIVES OF 2-PYRIDIN - 2 - IL - PIRAZOL - 3 (2H) -ONA, ITS PREPARATION AND ITS APPLICATION IN THERAPEUTICS AS HIF ACTIVATORSInfo
- Publication number
- NI201100133A NI201100133A NI201100133A NI201100133A NI201100133A NI 201100133 A NI201100133 A NI 201100133A NI 201100133 A NI201100133 A NI 201100133A NI 201100133 A NI201100133 A NI 201100133A NI 201100133 A NI201100133 A NI 201100133A
- Authority
- NI
- Nicaragua
- Prior art keywords
- group
- alkyl
- heterocycloalkyl
- hydrogen atom
- aryl
- Prior art date
Links
- 238000002360 preparation method Methods 0.000 title abstract 2
- 239000012190 activator Substances 0.000 title 1
- 239000003814 drug Substances 0.000 title 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 4
- 125000000592 heterocycloalkyl group Chemical group 0.000 abstract 3
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- 101100516554 Caenorhabditis elegans nhr-5 gene Proteins 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 125000001072 heteroaryl group Chemical group 0.000 abstract 1
- 238000002560 therapeutic procedure Methods 0.000 abstract 1
Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
La invención se refiere a los compuestos que responden a la fórmula (I): R representa un grupo -S02-NR3R4, un átomo de hidrógeno, un átomo de halógeno, un grupo -halógenoalquilo(C1-C5), un grupo -CO2R5 o un grupo SO2-R4 ; R1 representa un grupo heterocicloalquilo que no contiene átomo de nitrógeno, un grupo-W-cicloalquilo(C3-C6), un grupo -W-arilo, un grupo-W-heteroarilo, un grupo -W - heterocicloalquilo, un grupo -W-COOR5, un grupo -W-CONR5R6.; R2 representa un átomo de hidrógeno, un grupo -alquilo(C1-C5), un grupo -alquileno(C1-C5)-O- alquilo(C1-C5), un grupo -halógenoalquilo(C1-C5), un grupo -W-COOR5, un grupo -W-C(O)NHR5 o un grupo -W-C(O)-NR5R6; n representa 0, 1 ó 2 ; W es un grupo - alquileno(C1-C5)- o un grupo -cicloalquileno(C3-C6)- ; R3 y R4, idénticos o diferentes, representan, independientemente el uno del otro, un átomo de hidrógeno, un grupo - alquilo(C1 -C5), un grupo -cicloalquilo(C3-C6), un grupo -alquileno(C1 -C5) - O - alquilo(C1-C5), un arilo, un grupo -CH2-arilo, un heteroarilo, un heterocicloalquilo, un grupo -W-OH, un grupo -W-CHOH-CH2OH, un grupo -W-CO2R5, un grupo -W-NR5R6 o un grupo -W-O-(CH2)n-arilo; o bien R3 y R4 forman junto con el átomo de nitrógeno al que están unidos un grupo heterocicloalquilo ; R5 y R6, idénticos o diferentes, representan, independientemente el uno del otro, un átomo de hidrógeno, un grupo - alquilo (C1-C5) o un grupo halógenoalquilo(C1 -C5), así como su procedimiento de preparación y sus aplicaciones en terapéutica.The invention relates to the compounds that respond to formula (I): R represents a group -S02-NR3R4, a hydrogen atom, a halogen atom, a -halogenoalkyl group (C1-C5), a group -CO2R5 or a SO2-R4 group; R1 represents a heterocycloalkyl group containing no nitrogen atom, a -W-cycloalkyl group (C3-C6), a -W-aryl group, a -W-heteroaryl group, a -W-heterocycloalkyl group, a -W- group COOR5, a -W-CONR5R6 group; R2 represents a hydrogen atom, a -alkyl (C1-C5) group, a -alkylene (C1-C5) -O-alkyl (C1-C5) group, a -haloalkyl (C1-C5) group, a -W group -COOR5, a -WC (O) NHR5 group or a -WC (O) -NR5R6 group; n represents 0, 1 or 2; W is a group - (C1-C5) alkylene - or a -cycloalkylene (C3-C6) group -; R3 and R4, identical or different, represent, independently of each other, a hydrogen atom, a group - alkyl (C1-C5), a group -cycloalkyl (C3-C6), a group -alkylene (C1 -C5) - O-(C1-C5) alkyl, an aryl, a -CH2-aryl group, a heteroaryl, a heterocycloalkyl, a -W-OH group, a -W-CHOH-CH2OH group, a -W-CO2R5 group, a -W-NR5R6 group or -WO- (CH2) n-aryl group; or R3 and R4 together with the nitrogen atom to which they are attached form a heterocycloalkyl group; R5 and R6, identical or different, represent, independently of each other, a hydrogen atom, a group - alkyl (C1-C5) or a halogenoalkyl group (C1-C5), as well as their preparation process and their applications in therapy.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0807474A FR2940651B1 (en) | 2008-12-29 | 2008-12-29 | 2-PYRIDIN-2-YL-PYRAZOL-3 (2H) -ONE DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC USE AS HIF ACTIVATORS |
| FR0984092 | 2009-08-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NI201100133A true NI201100133A (en) | 2011-11-02 |
Family
ID=70471669
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NI201100133A NI201100133A (en) | 2008-12-29 | 2011-06-28 | DERIVATIVES OF 2-PYRIDIN - 2 - IL - PIRAZOL - 3 (2H) -ONA, ITS PREPARATION AND ITS APPLICATION IN THERAPEUTICS AS HIF ACTIVATORS |
Country Status (1)
| Country | Link |
|---|---|
| NI (1) | NI201100133A (en) |
-
2011
- 2011-06-28 NI NI201100133A patent/NI201100133A/en unknown
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