AR121078A1 - Derivados de arilamida con actividad antitumoral - Google Patents

Derivados de arilamida con actividad antitumoral

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Publication number
AR121078A1
AR121078A1 ARP210100120A ARP210100120A AR121078A1 AR 121078 A1 AR121078 A1 AR 121078A1 AR P210100120 A ARP210100120 A AR P210100120A AR P210100120 A ARP210100120 A AR P210100120A AR 121078 A1 AR121078 A1 AR 121078A1
Authority
AR
Argentina
Prior art keywords
group
alkyl group
halogen atom
hydrogen atom
optionally substituted
Prior art date
Application number
ARP210100120A
Other languages
English (en)
Inventor
Yoshiaki Isshiki
Fumio Watanabe
Masaki Tomizawa
Kihito Hada
Kazuo Hattori
Kenichi Kawasaki
Ikumi Hyodo
Toshihiro Aoki
Original Assignee
Chugai Pharmaceutical Co 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 Chugai Pharmaceutical Co Ltd filed Critical Chugai Pharmaceutical Co Ltd
Publication of AR121078A1 publication Critical patent/AR121078A1/es

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    • C07D211/06Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D265/00Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
    • C07D265/021,2-Oxazines; Hydrogenated 1,2-oxazines
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/16Amides, e.g. hydroxamic acids
    • A61K31/165Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
    • A61K31/166Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the carbon of a carboxamide group directly attached to the aromatic ring, e.g. procainamide, procarbazine, metoclopramide, labetalol
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
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    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
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Abstract

Compuestos derivados de aril-sulfonilamidas como agentes de estabilización del complejo RAF / MEK, una composición farmacéutica que comprende a uno de estos compuestos y su utilización en agentes terapéuticos para el tratamiento del cáncer. Reivindicación 1: Un compuesto representado por la fórmula general (1) o una sal farmacéuticamente aceptable del mismo, o un solvato farmacéuticamente aceptable de dicho compuesto o sal, en donde: el anillo A es un grupo representado por la fórmula general (2), (3), (4) ó (5) (en donde los enlaces indicados por *, ** y *** están unidos a -NH-, -CONH- y -CH₂-, respectivamente); X¹, X², X³, X⁴, X⁵ y X⁶ son respectiva e independientemente -CR²= o -N=; R² es un átomo de hidrógeno, un átomo halógeno, o un grupo alquilo C₁₋₆; R¹ es -S(=O)₂-NH-R⁸ o -S(=O)₂-R⁸; R⁸ es un átomo de hidrógeno, un grupo alquilo C₁₋₆ (el grupo alquilo C₁₋₆ es opcionalmente sustituido con un átomo halógeno, un grupo hidroxi, un grupo alcoxi C₁₋₆, un grupo cicloalquilo C₃₋₆ o un grupo heterocicloalquilo C₃₋₆), un grupo cicloalquilo C₃₋₆ monocíclico o bicíclico (el grupo cicloalquilo C₃₋₆ es opcionalmente sustituido con un grupo alquilo C₁₋₆ o un grupo alcoxi C₁₋₆), o un grupo heterocicloalquilo C₃₋₆ monocíclico o bicíclico; R³ es un átomo de hidrógeno, un grupo alquilo C₁₋₆ (el grupo alquilo C₁₋₆ es opcionalmente sustituido con un átomo halógeno, un grupo hidroxi o un grupo alcoxi C₁₋₆), un grupo cicloalquilo C₃₋₆ (el grupo cicloalquilo C₃₋₆ es opcionalmente sustituido con un átomo halógeno o un grupo alquilo C₁₋₆), o un grupo alcoxi C₁₋₆ (el grupo alcoxi C₁₋₆ es opcionalmente sustituido con un átomo halógeno, un grupo hidroxi o un grupo alcoxi C₁₋₆); R⁵ es un átomo halógeno o un grupo alquilo C₁₋₆; R⁶ es un átomo de hidrógeno, un átomo halógeno o un grupo alquilo C₁₋₆ y R⁴ es un átomo de hidrógeno, un átomo halógeno, un grupo alquilo C₁₋₆, un grupo alquenilo C₂₋₇, un grupo alquinilo C₂₋₇, un grupo cicloalquilo C₃₋₆ o un grupo alquiltio C₁₋₆, o R⁶ y R⁴ forman un anillo hetero de 5 miembros insaturado junto con los átomos de carbono a los cuales están unidos; R⁷ es un átomo de hidrógeno o un grupo alquilo C₁₋₆; y R⁹ es un átomo de hidrógeno, un átomo halógeno, o un grupo alquilo C₁₋₆.
ARP210100120A 2020-01-22 2021-01-20 Derivados de arilamida con actividad antitumoral AR121078A1 (es)

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