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Inhibitors of kras g12c mutant proteins

a technology of kras g12c and mutant proteins, which is applied in the field of inhibitors of kras g12c mutant proteins, can solve the problem of challenging the target of this gene with small molecules

Inactive Publication Date: 2018-05-24
ARAXES PHARMA LLC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The present invention provides compounds that can target and modify certain mutated proteins, such as KRAS, HRAS, and NRAS, which are associated with cancer and other diseases. These compounds can form a covalent bond with a specific amino acid residue in the protein, which can lead to inhibition of protein activity and cell proliferation. The invention also provides pharmaceutical compositions comprising these compounds for the treatment of cancer and other diseases associated with mutations in KRAS, HRAS, or NRAS proteins. Additionally, the invention also describes methods for using these compounds for the regulation of KRAS, HRAS, or NRAS protein activity and the preparation of labeled KRAS, HRAS, or NRAS proteins.

Problems solved by technology

Because these signals result in cell growth and division, overactive RAS signaling may ultimately lead to cancer.
However targeting this gene with small molecules is a challenge.

Method used

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  • Inhibitors of kras g12c mutant proteins
  • Inhibitors of kras g12c mutant proteins
  • Inhibitors of kras g12c mutant proteins

Examples

Experimental program
Comparison scheme
Effect test

example 1

Synthesis of 1-(4-(2′-chloro-5′-hydroxybiphenyl-4-yl)piperazin-1-yl)prop-2-en-1-one (1)

[0296]

6-Chloro-4′-(piperazin-1-yl)-[1,1′-biphenyl]-3-ol

[0297]A mixture of 3-bromo-4-chlorophenol (50 mg, 0.24 mmol), 1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)piperazine (70 mg, 0.24 mmol), and Pd(dppf)Cl2.CH2Cl2 (20 mg, 0.024 mmol) in co-solvent of dioxane / saturated NaHCO3 (3 mL, 2:1) was stirred at 120° C. in microwave reactor for 5 minutes. The mixture was diluted with DCM and washed with water. The organic layer was dried over Na2SO4, filtered, and concentrated in vacuo to afford the desired product.

1-(4-(2′-Chloro-5′-hydroxy-[1,1′-biphenyl]-4-yl)piperazin-1-yl)prop-2-en-1-one

[0298]To a stirred solution of 6-chloro-4′-(piperazin-1-yl)-[1,1′-biphenyl]-3-ol dissolved in DCM (10 mL) triethylamine was added, followed by the addition of acryloyl chloride (22 mg, 0.24 mmol) at 0° C. The mixture was stirred for 30 minutes, diluted with DCM, and washed with saturated NaHCO3. The organic...

example 2

Synthesis of 1-(4-(4-(2-chloro-5-hydroxyphenyl)-1H-indazol-7-yl)piperazin-1-yl)prop-2-en-1-one (24)

[0299]

1-Bromo-4-fluoro-2-methyl-3-nitrobenzene

[0300]A mixture of 1-fluoro-3-methyl-2-nitrobenzene (18 g, 116 mmol) and TFA (75 mL) was cooled to 0° C. and 98% H2SO4 aqueous solution (75 mL) was added, followed by NBS (31 g, 174 mmol) in small portions within 1 h. The mixture was stirred at 0° C. for 20 min, and at room temperature for 3 h. The mixture was poured in to a mixture of water (300 g) and ice (300 g), and the pH was adjusted to 7-8 using NaHCO3. The solid was filtered and washed with hexanes / ethyl acetate (9:1, 300 mL). The organic phase was separated and the aqueous phase was extracted with hexanes / ethyl acetate (9:1, 400 mL). The combined organic layer was washed with Na2S2O3 aqueous solution (2×200 mL) and brine (200 mL), dried over Na2SO4, filtered, and concentrated in vacuo. The remaining solid was dissolved in 400 mL of hexanes and dark oil at the bottom of flask was di...

example 3

Synthesis of 1-(4-((2′-chloro-5′-hydroxy-[1,1′-biphenyl]-4-yl)methyl)piperazin-1-yl)prop-2-en-1-one (17)

[0306]

tert-Butyl 4-(4-bromobenzyl)piperazine-1-carboxylate

[0307]A mixture of 1-bromo-4-(bromomethyl)benzene (250 mg, 1 mmol), tert-butyl piperazine-1-carboxylate (186.3 mg, 1 mmol) and diisopropyl ethyl amine (156 mg, 1.2 mmol) in DCM was stirred at RT overnight. The mixture was diluted with DCM and washed with water. The organic layer was dried over Na2SO4, filtered, and concentrated in vacuo. The residue was purified via Isolera One (ethyl acetate / hexane=0-50%) to afford the desired compound.

1-(4-(4-Bromobenzyl)piperazin-1-yl)prop-2-en-1-one

[0308]A solution of tert-butyl 4-(4-bromobenzyl)piperazine-1-carboxylate in 50% TAF in DCM (5 mL) was stirred at RT for 1 h. The solution was concentrated in vacuo and the residue was re-dissolved in DCM, and washed with saturated NaHCO3. The organic layer was dried over Na2SO4, filtered, and concentrated in vacuo. The residue was re-dissolve...

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Abstract

Compounds having activity as inhibitors of G12C mutant KRAS protein are provided. The compounds have the following structure (I):or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof, wherein R1, R2, R3a, R3b, R4a, R4b, G1, G2, L, m1, m2 and E are as defined herein. Methods associated with preparation and use of such compounds, pharmaceutical compositions comprising such compounds and methods to modulate the activity of G12C mutant KRAS protein for treatment of disorders, such as cancer, are also provided.

Description

BACKGROUNDTechnical Field[0001]The present invention is generally directed to novel compounds and methods for their preparation and use as therapeutic or prophylactic agents, for example for treatment of cancer.Description of the Related Art[0002]RAS represents a group of closely related monomeric globular proteins of 189 amino acids (21 kDa molecular mass) which are associated with the plasma membrane and which bind either GDP or GTP. RAS acts as a molecular switch. When RAS contains bound GDP, it is in the resting or off position and is “inactive”. In response to exposure of the cell to certain growth promoting stimuli, RAS is induced to exchange its bound GDP for a GTP. With GTP bound, RAS is “switched on” and is able to interact with and activate other proteins (its “downstream targets”). The RAS protein itself has a very low intrinsic ability to hydrolyze GTP back to GDP, thus turning itself into the off state. Switching RAS off requires extrinsic proteins termed GTPase-activat...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): C07D401/04C07D295/185C07D295/10C07D213/75C07D231/56C07D239/42
CPCC07D213/75C07D231/56C07D401/04C07D295/185C07D239/42C07D295/10A61P1/00A61P1/18A61P35/00A61P35/02
Inventor LI, LIANSHENGFENG, JUNREN, PINGDALIU, YI
Owner ARAXES PHARMA LLC
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