CO4810228A1 - DERIVATIVES OF PYRAZOLE PIRIDAZINE, PROCESSES FOR ITS PREPARATION AND PHARMACEUTICAL COMPOSITIONS THAT CONTAIN THEM - Google Patents

DERIVATIVES OF PYRAZOLE PIRIDAZINE, PROCESSES FOR ITS PREPARATION AND PHARMACEUTICAL COMPOSITIONS THAT CONTAIN THEM

Info

Publication number
CO4810228A1
CO4810228A1 CO99005569A CO99005569A CO4810228A1 CO 4810228 A1 CO4810228 A1 CO 4810228A1 CO 99005569 A CO99005569 A CO 99005569A CO 99005569 A CO99005569 A CO 99005569A CO 4810228 A1 CO4810228 A1 CO 4810228A1
Authority
CO
Colombia
Prior art keywords
carbon atoms
alkyl
atoms
alkoxy
derivatives
Prior art date
Application number
CO99005569A
Other languages
Spanish (es)
Inventor
Paul Beswick
Ian Campbell
Mathews Neil
Alan Naylor
Original Assignee
Glaxo Group Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Glaxo Group Ltd filed Critical Glaxo Group Ltd
Priority to CO99005569A priority Critical patent/CO4810228A1/en
Publication of CO4810228A1 publication Critical patent/CO4810228A1/en

Links

Landscapes

  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

Los compuestos de la fórmula (I)y derivados farmacéuticamente aceptables de los mismos, en los cuales:R° es halógeno, alquilo de 1 a 6 átomos de carbono, alcoxi de 1 a 6 átomos de carbono, alcoxi de 1 a 6 átomos de carbono substituido por uno o más átomos de flúor, o O(CH2 )n NR4 R5 ;R1 y R2 se seleccionan independientemente de H, alquilo de 1 a 6 átomos de carbono, alquilo de 1 a 6 átomos de carbono substituido por uno o más átomos de flúor, alcoxi de 1 a 6 átomos de carbono, hidroxialquilo de 1 a 6 átomos de carbono, S-alquilo de 1 a 6 átomos de carbono, C(O)H, C(O)alquilo de 1 a 6 átomos de carbono, alquilsulfonilo de 1 a 6 átomos de carbono, alcoxi de 1 a 6 átomos de carbono substituido por uno o más átomos de flúor, O(CH2 )n CO2 -alquilo de 1 a 6 átomos de carbono, O(CH2 )n S-alquilo de 1 a 6 átomos de carbono, (CH2 )n NR4 R5 , (CH2 )n S-alquilo de 1 a 6 átomos de carbono o C(O)NR4 R5 ; con la condición que cuando R° sea un halógeno y esté en la posición 4, al menos uno de R1 y R2 es alquilsulfonilo de 1 a 6 átomos de carbono, alcoxi de 1 a 6 átomos de carbono substituido por uno o más átomos de flúor, O(CH2 )n CO2 -alquilo de 1 a 6 átomos de carbono, O(CH2 )n S-alquilo de 1 a 6 átomos de carbono (CH2 )n NR4 R5 o (CH2 )n S-alquilo de 1 a 6 átomos de carbono, C(O)NR4 R5 ;R3 es alquilo de 1 a 6 átomos de carbono o NH2 ;R4 y R5 se seleccionan independientemente de H, o alquilo de 1 a 6 átomos de carbono o, juntos con el átomo de nitrógeno al cual están unidos, forman un anillo saturado de 4 a 8 miembros; yn es un número de 1 a 4.Compounds of formula (I) and pharmaceutically acceptable derivatives thereof, in which: R ° is halogen, alkyl of 1 to 6 carbon atoms, alkoxy of 1 to 6 carbon atoms, alkoxy of 1 to 6 carbon atoms carbon substituted by one or more fluorine atoms, or O (CH2) n NR4 R5; R1 and R2 are independently selected from H, alkyl of 1 to 6 carbon atoms, alkyl of 1 to 6 carbon atoms substituted by one or more fluorine atoms, alkoxy of 1 to 6 carbon atoms, hydroxyalkyl of 1 to 6 carbon atoms, S-alkyl of 1 to 6 carbon atoms, C (O) H, C (O) alkyl of 1 to 6 atoms of carbon, alkylsulfonyl of 1 to 6 carbon atoms, alkoxy of 1 to 6 carbon atoms substituted by one or more fluorine atoms, O (CH2) n CO2 -alkyl of 1 to 6 carbon atoms, O (CH2) n S -alkyl of 1 to 6 carbon atoms, (CH2) n NR4 R5, (CH2) n S-alkyl of 1 to 6 carbon atoms or C (O) NR4 R5; with the proviso that when R ° is a halogen and is in the 4-position, at least one of R1 and R2 is alkylsulfonyl of 1 to 6 carbon atoms, alkoxy of 1 to 6 carbon atoms substituted by one or more fluorine atoms , O (CH2) n CO2-alkyl of 1 to 6 carbon atoms, O (CH2) n S-alkyl of 1 to 6 carbon atoms (CH2) n NR4 R5 or (CH2) n S-alkyl of 1 to 6 carbon atoms, C (O) NR4 R5; R3 is alkyl of 1 to 6 carbon atoms or NH2; R4 and R5 are independently selected from H, or alkyl of 1 to 6 carbon atoms or, together with the nitrogen atom to which they are attached, they form a 4-8 membered saturated ring; and n is a number from 1 to 4.

CO99005569A 1999-02-02 1999-02-02 DERIVATIVES OF PYRAZOLE PIRIDAZINE, PROCESSES FOR ITS PREPARATION AND PHARMACEUTICAL COMPOSITIONS THAT CONTAIN THEM CO4810228A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CO99005569A CO4810228A1 (en) 1999-02-02 1999-02-02 DERIVATIVES OF PYRAZOLE PIRIDAZINE, PROCESSES FOR ITS PREPARATION AND PHARMACEUTICAL COMPOSITIONS THAT CONTAIN THEM

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CO99005569A CO4810228A1 (en) 1999-02-02 1999-02-02 DERIVATIVES OF PYRAZOLE PIRIDAZINE, PROCESSES FOR ITS PREPARATION AND PHARMACEUTICAL COMPOSITIONS THAT CONTAIN THEM

Publications (1)

Publication Number Publication Date
CO4810228A1 true CO4810228A1 (en) 1999-06-30

Family

ID=40933408

Family Applications (1)

Application Number Title Priority Date Filing Date
CO99005569A CO4810228A1 (en) 1999-02-02 1999-02-02 DERIVATIVES OF PYRAZOLE PIRIDAZINE, PROCESSES FOR ITS PREPARATION AND PHARMACEUTICAL COMPOSITIONS THAT CONTAIN THEM

Country Status (1)

Country Link
CO (1) CO4810228A1 (en)

Similar Documents

Publication Publication Date Title
AR036093A1 (en) COMPOUNDS DERIVED FROM TIAZOLIDINILO, PIRROLIDINILO, OXAZOLIDINILO, PIPERIDILO, MORFOLINILO AND TIOMORFOLINILO, ITS USE, PHARMACEUTICAL COMPOSITIONS THAT INCLUDE THEM, AND INTERMEDIARY COMPOUNDS
CO5640117A2 (en) 2,4-DIAMONOPIRIMIDINE DERIVATIVES
NO20013379D0 (en) 4-oxo-1,4-dihydro-3-quinolinecarboxamides as antiviral agents
HRP20000896B1 (en) Adenosine derivatives
TW200612920A (en) Novel imidazolidine derivatives
UY26727A1 (en) USEFUL TROPANIC DERIVATIVES IN THERAPY
CO5200848A1 (en) DERIVATIVES OF 3 (5) -UREIDO-PIRAZOL, PROCESS FOR ITS PREPARATION AND ITS USE AS ANTITUMOR AGENTS
ES2046202T3 (en) A PROCEDURE FOR PREPARING A DISTAMICINE ANALOG A.
AR009413A1 (en) A COMPOUND, WHICH IS A DERIVATIVE OF BENZOHETEROCICLICO DISTAMICINA, ITS USE, A PROCEDURE TO PRODUCE IT AND A PHARMACEUTICAL COMPOSITION THAT INCLUDES IT
RS51674B (en) Piperidin-4-yl-pyridazin-3-ylamine derivatives as fast dissociating dopamine 2 receptor antagonists
YU74792A (en) HERBICIDES
NO20033145D0 (en) Purine derivatives as purinergic receptor antagonists
CO5631434A2 (en) DERIVATIVES OF PIRIDINA-CARBOXAMIDA AND ITS USE AS PESTICIDES
GB9806692D0 (en) Benzoheterocyclic distamycin derivatives, process for preparing them and their use as antitumour agents
CO5550439A2 (en) COMPOUNDS DERIVED FROM ARILSULFONIL-PIPERAZINA THAT HAVE AFFINITY TO THE 5-HT6 RECEPTOR AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
AR005672A1 (en) DERIVATIVES OF DISTAMICINE, PROCESS TO PREPARE THEM, AND THEIR USE AS ANTI-TUMOR AND ANTIVIRAL AGENTS.
DE60011269D1 (en) AZAIDOLE WITH SEROTONIN RECEPTOR AFFINITY
DE60336735D1 (en) NEW BIOLOGICAL MOLEKÜ LE
AR007108A1 (en) ANTI-TUMOR AND ANTIVIRAL RENTAL AGENTS, PROCEDURE FOR THEIR PREPARATION, USE OF THE SAME FOR THE MANUFACTURE OF A MEDICINAL PRODUCT AND PHARMACEUTICAL COMPOSITION CONTAINING SUCH AGENTS.
CO5040004A1 (en) 2-4-DIAMINO-1,3,5-TRIAZINAS, ITS PREPARATION AND EMPLOYMENT AS HERBICIDES AND PHYTO-REGULATORS
ES2083625T3 (en) DERIVATIVES OF N-FENILTIOUREA AND PHARMACEUTICAL USE THEREOF.
HRP20030610B1 (en) Process for the preparation of mesylates of piperazine derivatives
AR043487A1 (en) FUSIONED HEREROCICLES OF PYRIMIDINE AND USES OF THE SAME
RS50905B (en) Benzopyran derivatives substituted with secondary amines including tetrazole, method for the preparation thereof and pharmaceutical compositions containing them
CO4810228A1 (en) DERIVATIVES OF PYRAZOLE PIRIDAZINE, PROCESSES FOR ITS PREPARATION AND PHARMACEUTICAL COMPOSITIONS THAT CONTAIN THEM