Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Macrocyclic compounds and their use as kinase inhibitors

a technology of macrocyclic compounds and kinase inhibitors, applied in the field of macrocyclic compounds, can solve the problems of adversely affecting patient health, poor prognosis, and elevated levels of circulating cytokines, and achieve the effect of efficient treatment and few associated clinical side effects

Active Publication Date: 2010-07-29
INCYTE CORP
View PDF2 Cites 25 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The present invention provides compounds of Formula I, which can be used to treat various conditions associated with JAK / ALK kinases. These compounds can inhibit the activity of these kinases and are therefore useful in treating diseases such as cancer. The invention also provides pharmaceutical compositions containing these compounds and methods of using them for treating JAK / ALK-related conditions.

Problems solved by technology

In addition, JAK2 deficiency resulted in cell-type specific deficiencies in the signaling of some cytokines such as those required for definitive erythropoiesis (Neubauer, H., A. Cumano, et al.
Importantly, activation of STAT signaling, as well as other pathways downstream of JAKs (e.g. Akt), has been correlated with poor prognosis in many cancer types (Bowman, T., et al.
Moreover, elevated levels of circulating cytokines that signal through JAK / STAT may adversely impact patient health as they are thought to play a causal role in cachexia and / or chronic fatigue.
It has been known that certain therapeutics can cause immune reactions such as skin rash or diarrhea in some patients.
For some patients, these immune reactions may be bothersome, but for others, the immune reactions such as rash or diarrhea may result in the inability to continue treatment.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Macrocyclic compounds and their use as kinase inhibitors
  • Macrocyclic compounds and their use as kinase inhibitors
  • Macrocyclic compounds and their use as kinase inhibitors

Examples

Experimental program
Comparison scheme
Effect test

example 1

6-Chloro-15-oxa-2,4,8,23-tetraazatetracyclo[15.3.1.1(3,7).1(10,14)]tricosa-1(21),3(23),4,6,10(22),11,13,17,19-nonaene trifluoroacetate

[0674]

Step A: 2,5-Dichloro-N-(3-methoxybenzyl)pyrimidin-4-amine

[0675]

[0676]To a solution of 3-methoxybenzylamine (0.75 g, 5.4 mmol) and 2,4,5-trichloropyrimidine (1.1 g, 6.0 mmol) in N,N-dimethylformamide (20 mL) was added potassium carbonate (2.3 g, 16 mmol). The resulting mixture was stirred overnight at room temperature. The reaction was quenched with water. Ethyl acetate (“EtOAc”) was added and the layers were separated. The aqueous layer was extracted with EtOAc once. The combined organic layers were washed with water and brine successively, then dried (Na2SO4), filtered, and concentrated. The crude product was purified by silica gel column chromatography to give the desired product as a white powder (1.43 g, 92%). LCMS for C12H12ClN3O (M+H)+: m / z=284.0, 286.0.

Step B: [3-({5-Chloro-4-[(3-methoxybenzyl)amino]pyrimidin-2-yl}amino)phenyl]methanol

[06...

example 2

6-Chloro-15-oxa-2,4,8,24-tetraazatetracyclo[16.3.1.1(3,7).1(10,14)]tetracosa-1(22),3(24),4,6,10(23),11,13,18,20-nonaene trifluoroacetate

[0682]

Step A: 2-(3-Aminophenyl)ethanol

[0683]

[0684]Into a pressure bottle were added 2-(3-nitrophenyl)ethanol (3.0 g, 18 mmol) and methanol (100 mL) and 10% palladium on carbon (0.1 g, 0.08 mmol). The reaction mixture was hydrogenated at 45 psi overnight. The resultant mixture was filtered and concentrated to provide the desired product (2.44 g, 99%) as a white solid. LCMS for C8H12NO (M+H)+: m / z=138.1.

Step B: 2-[3-({5-Chloro-4-[(3-methoxybenzyl)amino]pyrimidin-2-yl}amino)phenyl]ethanol

[0685]

[0686]Into a reaction flask were added 2,5-dichloro-N-(3-methoxybenzyl)pyrimidin-4-amine (0.33 g, 1.2 mmol) (prepared according to Example 1, step A), 1,4-dioxane (20 mL), 2-(3-aminophenyl)ethanol (0.22 g, 1.6 mmol), and p-toluenesulfonic acid monohydrate (0.080 g, 0.42 mmol). The mixture was heated at 105° C. for 3 hours and then an aqueous solution of NaHCO3 (s...

example 3

6-Chloro-16-thia-2,4,8,15,23-pentaazatetracyclo[15.3.1.1(3,7).1(10,14)]tricosa-1(21),3(23),4,6,10(22),11,13,17,19-nonaene 16,16-dioxide trifluoroacetate

[0690]

Step A: tert-Butyl(3-{[(2,5-dichloropyrimidin-4-yl)amino]methyl}phenyl)carbamate

[0691]

[0692]To a solution of tert-butyl [3-(aminomethyl)phenyl]carbamate (0.50 g, 2.2 mmol) and 2,4,5-trichloropyrimidine (0.45 g, 2.5 mmol) in N,N-dimethylformamide (6 mL) was added potassium carbonate (0.62 g, 4.5 mmol). The resultant mixture was stirred overnight at room temperature. The reaction was quenched with water. EtOAc was added and the layers were separated. The aqueous layer was extracted with EtOAc twice. The combined organic layers were washed with water and brine successively, then dried (Na2SO4), filtered, and concentrated. The resulted residue was triturated with methylene chloride and hexanes to give the desired product as an off-white powder (0.75 g, 90%). LCMS for C12H11Cl2N4O2 (M-tBu+H)+: m / z=313.0, 315.0.

Step B: N-(3-Aminobenz...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
temperatureaaaaaaaaaa
temperatureaaaaaaaaaa
pHaaaaaaaaaa
Login to View More

Abstract

The present invention relates to macrocyclic compounds of Formula I:or pharmaceutically acceptable salts thereof or quaternary ammonium salts thereof wherein constituent members are provided hereinwith, as well as their compositions and methods of use, which are JAK / ALK inhibitors useful in the treatment of JAK / ALK-associated diseases including, for example, inflammatory and autoimmune disorders, as well as cancer.

Description

[0001]This application claims benefit of priority to U.S. provisional patent application Ser. No. 61 / 146, 824 filed Jan. 23, 2009, which is hereby incorporated by reference in its entirety.FIELD OF THE INVENTION[0002]The present invention relates to macrocyclic compounds, and compositions thereof as well as methods of use the same for treatment of Janus Kinase and / or Anaplastic Lymphoma Kinase (JAK / ALK)-associated diseases including, for example, inflammatory disorders, autoimmune disorders, skin disorders, myeloid proliferative disorders, as well as cancer.BACKGROUND OF THE INVENTION[0003]Protein kinases (PKs) are a group of enzymes that regulate diverse, important biological processes including cell growth, survival and differentiation, organ formation and morphogenesis, neovascularization, tissue repair and regeneration, among others. Protein kinases exert their physiological functions through catalyzing the phosphorylation of proteins (or other substrates such as lipids) and the...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(United States)
IPC IPC(8): A61K31/4985C07D498/02C07D487/22A61P35/00A61P37/06
CPCC07D487/22C07D471/22A61P35/00A61P37/06
Inventor COMBS, ANDREW PAULSPARKS, RICHARD B.YUE, EDDY WAI TSUNFENG, HAOBOWER, MICHAEL JASONZHU, WENYU
Owner INCYTE CORP
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com