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PE20161073A1 - Amino-heteroaril-benzamidas como inhibidores de cinasa - Google Patents

Amino-heteroaril-benzamidas como inhibidores de cinasa

Info

Publication number
PE20161073A1
PE20161073A1 PE2016000507A PE2016000507A PE20161073A1 PE 20161073 A1 PE20161073 A1 PE 20161073A1 PE 2016000507 A PE2016000507 A PE 2016000507A PE 2016000507 A PE2016000507 A PE 2016000507A PE 20161073 A1 PE20161073 A1 PE 20161073A1
Authority
PE
Peru
Prior art keywords
heteroaryl
amino
benzamides
kinase inhibitors
halogen
Prior art date
Application number
PE2016000507A
Other languages
English (en)
Inventor
Jeffrey T Bagdanoff
Shejin Zhu
Wooseok Han
Zilin Huang
Qun Jiang
Jeff Xianming Jin
Xiang Kou
Patrick Lee
Mika Lindvall
Zhongcheng Min
Yue Pan
Sabina Pecchi
Keith Bruce Pfister
Daniel Poon
Vivek Rauniyar
Xiaojing Michael Wang
Qiong Zhang
Jianguang Zhou
Yu Ding
Original Assignee
Novartis Ag
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 Novartis Ag filed Critical Novartis Ag
Publication of PE20161073A1 publication Critical patent/PE20161073A1/es

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    • C07D405/14Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
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    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
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    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4418Non condensed pyridines; Hydrogenated derivatives thereof having a carbocyclic group directly attached to the heterocyclic ring, e.g. cyproheptadine
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    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
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    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
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    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/4545Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
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    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/553Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one oxygen as ring hetero atoms, e.g. loxapine, staurosporine
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Abstract

Se refiere a compuestos amino-heteroaril-benzamidas de formula I donde R1 es cicloalquilo C3-C8, fenilo, entre otros; L es un enlace, alquileno C1-C4, entre otros; X e Y son H, D, halogeno, entre otros; R2 es H, alquilo C1-C4, entre otros; R5 es –CO-R5a o R5a; R5a es cicloalquilo C3-C8, fenilo, entre otros; Z es N o CR4; R4 es H, D, halogeno, entre otros; R6 es H, D, halogeno, entre otros. Tambien se refiere a una composicion farmaceutica y a un metodo de tratamiento. Dichos compuestos son inhibidores de ERK1 y ERK2, siendo utiles en el tratamiento del cancer
PE2016000507A 2013-11-01 2014-10-29 Amino-heteroaril-benzamidas como inhibidores de cinasa PE20161073A1 (es)

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US201361898761P 2013-11-01 2013-11-01
CN2014088409 2014-10-11

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PE20161073A1 true PE20161073A1 (es) 2016-10-30

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KR (1) KR101910720B1 (es)
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