AR046308A1 - Derivados amida - Google Patents

Derivados amida

Info

Publication number
AR046308A1
AR046308A1 ARP040103862A ARP040103862A AR046308A1 AR 046308 A1 AR046308 A1 AR 046308A1 AR P040103862 A ARP040103862 A AR P040103862A AR P040103862 A ARP040103862 A AR P040103862A AR 046308 A1 AR046308 A1 AR 046308A1
Authority
AR
Argentina
Prior art keywords
alkyl
alkoxy
alkylamino
amino
halogen
Prior art date
Application number
ARP040103862A
Other languages
English (en)
Inventor
Dearg Brown
Ian Nash
Original Assignee
Schuckmann Alfred Von
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=29595715&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AR046308(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Schuckmann Alfred Von filed Critical Schuckmann Alfred Von
Publication of AR046308A1 publication Critical patent/AR046308A1/es

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    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/626—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B
    • C04B35/63—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B using additives specially adapted for forming the products, e.g.. binder binders
    • C04B35/632—Organic additives
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    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
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    • C07D239/88—Oxygen atoms
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  • Urology & Nephrology (AREA)

Abstract

Compuestos útiles para el tratamiento de enfermedades o condiciones médicas mediadas por citoquinas. Procesos para su preparación, composiciones farmacéuticas que lo contienen o sales del mismo aceptables para uso farmacéutico. Reivindicación 1: Un compuesto de la fórmula (1), caracterizado porque m es 0, 1 ó 2; R1 es halógeno, oxhidrilo, ciano, trifluorometilo, trifluorometoxi, alquilo C1-6, alcoxi C1-6, alquenilo C2-6, alquinilo C2-6, alcanoilo C2-6, alquiltio C1-6, alquilsulfinilo C1-6, alquilsulfonilo C1-6, hidroxialcoxi C2-6, amino-alcoxi C2-6, ciano-alcoxi C2-6, alquilamino C1-6-alcoxi C2-6, di-[alquil C1-6]amino-alcoxi C2-6, alcoxi C1-6-alcoxi C2-6, carbamoil-alcoxi C1-6, N-alquil C1-6carbamoil-alcoxi C1-6, amino-alquilo C1-6, alquilamino C1-6-alquilo C1-6, di[alquil C1-6]amino-alquilo C1-6, carbamoil-alquilo C1-6, N-alquil C1-6carbamoil-alquilo C1-6, hidroxi-alquilamino C2-6, ciano-alquilamino C2-6, halógeno-alquilamino C2-6, amino-alquilamino C2-6, alcoxi C1-6- alquilamino C2-6, alquilamino C1-6-alquilamino C2-6, di-[alquil C1-6]aminoalquilamino C2-6, heteroarilo, heteroaril-alquilo C1-6, heteroariloxi, heteroaril-alcoxi C1-6, heteroarilamino, heterociclilo, heterociclil-alquilo C1-6, heterocicliloxi, heterociclil-alcoxi C1-6 y heterociclilamino, y donde cualquier grupo arilo, heteroarilo o heterociclilo en un sustituyente R1 puede llevar opcionalmente 1 ó 2 sustituyentes que se seleccionan entre oxhidrilo, halógeno, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-6, cicloalquil C3-6-alquilo C1-6, cicloalquil C3-6-alcoxi C1-6, alcoxi C1-6, carboxi, alcoxi C1-6carbonilo, alcoxi C1-6carbonil-alquilo C1-6, N-alquil C1-6carbamoilo, N,N-di-[alquil C1-6]carbamoilo, alcanoilo C2-6, amino, alquilamino C1-6, di-[alquil C1-6]amino, halógeno-alquilo C1-6, hidroxi-alquilo C1-6, alcoxi C1-6-alquilo C1-6, ciano-alquilo C1-6, carboxi-alquilo C1-6, amino-alquilo C1-6, alquilamino C1-6-alquilo C1-6 y di-[alquil C1-6]amino-alquilo C1-6, y donde cualquiera de los sustituyentes R1 que se definieron aquí anteriormente que comprende un grupo CH2 que está unido a 2 átomos de carbono o un grupo CH3 que está unido a un átomo de carbono o de nitrógeno puede llevar opcionalmente sobre cada uno de dichos grupos CH2 o CH3 uno o más sustituyentes que se seleccionan entre halógeno, oxhidrilo, amino, trifluorometilo, trifluorometoxi, oxo, carboxi, carbamoilo, acetamido, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-6, cicloalcoxi C3-6, alcoxi C1-6, alquilamino C1-6, di-[alquil C1-6]amino, hidroxi-alquilo C1-6, alcoxi C1-6-alquilo C1-6, halógeno-alquilo C1-6, alcoxi C1-6-alcoxi C2-6, alcoxi C1-6carbonilo, carbamoilo, N-alquil C1-6carbamoilo, N,N-di-[alquil C1- 6]carbamoilo, sulfonilo C1-6, sulfamoilo C1-6, heteroarilo, heteroaril-alquilo C1-6, heterociclilo y heterocicliloxi, y donde cualquier grupo heterociclilo en un sustituyente R1 puede llevar opcionalmente 1 ó 2 sustituyentes oxo o tioxo; R2 es halógeno, trifluorometilo o alquilo C1-6; R3 es hidrógeno, halógeno o alquilo C1-6; y R4 es cicloalquilo C3-6, y R4 opcionalmente puede estar sustituido con uno o más sustituyentes que se seleccionan entre halógeno, oxhidrilo, amino, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alcoxi C1-6, alquilamino C1-6 y di-[alquil C1-6]amino; o una sal del mismo aceptable para uso farmacéutico.
ARP040103862A 2003-10-24 2004-10-22 Derivados amida AR046308A1 (es)

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GBGB0324790.5A GB0324790D0 (en) 2003-10-24 2003-10-24 Amide derivatives

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AR046308A1 true AR046308A1 (es) 2005-11-30

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AR (1) AR046308A1 (es)
AT (1) ATE499347T1 (es)
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CA (1) CA2543351C (es)
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UY (1) UY28578A1 (es)
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US20070043065A1 (en) 2007-02-22
CA2543351C (en) 2012-09-11
SA04250351B1 (ar) 2009-06-01
TW200524882A (en) 2005-08-01
MXPA06004465A (es) 2006-06-20
SG147409A1 (en) 2008-11-28
KR101127697B1 (ko) 2012-04-12
TWI343378B (en) 2011-06-11
AU2004285749B2 (en) 2008-10-30
CN1898216A (zh) 2007-01-17
ES2359409T3 (es) 2011-05-23
IL175065A (en) 2011-09-27
MY140729A (en) 2010-01-15
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HK1091830A1 (en) 2007-01-26
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GB0324790D0 (en) 2003-11-26
IS8450A (is) 2006-05-11
AU2004285749A1 (en) 2005-05-12
KR20060114335A (ko) 2006-11-06
CN103012376A (zh) 2013-04-03
ATE499347T1 (de) 2011-03-15
EP1682520A1 (en) 2006-07-26
UA83867C2 (ru) 2008-08-26
RU2006117326A (ru) 2007-12-10
EP1682520B1 (en) 2011-02-23
JP4987478B2 (ja) 2012-07-25
CA2543351A1 (en) 2005-05-12
UY28578A1 (es) 2005-06-30
BRPI0415746A (pt) 2006-12-19
IL175065A0 (en) 2006-08-20
DE602004031543D1 (de) 2011-04-07
US7750154B2 (en) 2010-07-06
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