WO2018102453A1 - Substituted pyrazole compounds and methods of using them for treatment of hyperproliferative diseases - Google Patents

Substituted pyrazole compounds and methods of using them for treatment of hyperproliferative diseases Download PDF

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Publication number
WO2018102453A1
WO2018102453A1 PCT/US2017/063774 US2017063774W WO2018102453A1 WO 2018102453 A1 WO2018102453 A1 WO 2018102453A1 US 2017063774 W US2017063774 W US 2017063774W WO 2018102453 A1 WO2018102453 A1 WO 2018102453A1
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WIPO (PCT)
Prior art keywords
methyl
pyrazole
optionally substituted
cancer
thiazol
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PCT/US2017/063774
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English (en)
French (fr)
Inventor
Arshad M. Siddiqui
Stephane Ciblat
Martin DERY
Lea CONSTANTINEUA-FORGET
Chantal Grand-Maitre
Nicolas BRUNEAU-LATOUR
Gerald W. Shipps
Alan B. Cooper
Vibha Oza
Matthew W. KOSTURA
Michael Luther
Jedd LEVINE
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Bantam Pharmaceutical LLC
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Bantam Pharmaceutical LLC
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Priority to EP17876486.6A priority Critical patent/EP3548482A4/en
Priority to US16/465,136 priority patent/US11325903B2/en
Priority to IL266930A priority patent/IL266930B2/en
Priority to CN201780084999.4A priority patent/CN110603254B/zh
Priority to CN202410345199.5A priority patent/CN118930533A/zh
Priority to JP2019528861A priority patent/JP7373992B2/ja
Priority to MX2019006299A priority patent/MX2019006299A/es
Priority to BR112019011044-5A priority patent/BR112019011044A2/pt
Priority to NZ754827A priority patent/NZ754827B2/en
Priority to RU2019120233A priority patent/RU2787994C2/ru
Application filed by Bantam Pharmaceutical LLC filed Critical Bantam Pharmaceutical LLC
Priority to AU2017366901A priority patent/AU2017366901B2/en
Priority to CA3081983A priority patent/CA3081983A1/en
Publication of WO2018102453A1 publication Critical patent/WO2018102453A1/en
Anticipated expiration legal-status Critical
Priority to US17/741,153 priority patent/US20230076820A1/en
Ceased legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/08—Bridged systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4196—1,2,4-Triazoles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/425—Thiazoles
    • A61K31/427—Thiazoles not condensed and containing further heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D451/00—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
    • C07D451/02—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof

Definitions

  • This disclosure relates to the field of compounds, pharmaceutical compositions comprising them, and methods of using the compounds and compositions. This disclosure relates more particularly to methods for using certain compounds for the treatment of hyperproliferative disorders such as cancer.
  • Cancer an uncontrolled proliferation of cells, is a multifactorial disease characterized by tumor formation, growth, and in some instances, metastasis. In the United States this year, over 1.5 million people will be diagnosed with cancer, and more than 500,000 people will die from cancer. Overall it is estimated that at least one in three people will develop some form of cancer during their lifetime. There are more than 200 different histopathological types of cancer, with breast, lung, colorectal, and prostate accounting for over half of all new cases in the U.S. Current cancer therapies vary depending upon the localization and stage of the cancer but generally include a combination of surgery, systemic therapy, radiation therapy, and chemotherapy. Despite the effort that has been devoted to the development of anti-cancer strategies, many of them remain unefficacious for specific cancers.
  • the uncontrolled cell proliferation that represents the essence of cancer involves not only deregulated control of cell proliferation but also corresponding adjustments of energy metabolism in order to fuel cell growth and division.
  • the reprogramming of cell metabolism is emerging as an important molecular hallmark of cancer cells. Under aerobic conditions, normal cells process glucose, first to pyruvate via glycolysis in the cytosol and thereafter to carbon dioxide in the mitochondria; under anaerobic conditions, glycolysis is favored and relatively little pyruvate is dispatched to the oxygen-consuming mitochondria.
  • growth factors and nutrients are abundant, oncogenic signaling pathways direct enhanced metabolism leading to increased synthesis of macromolecules such as lipids, proteins and nucleic acids. The net effect is the support of cell growth and proliferation.
  • Cancer cells can reprogram their glucose metabolism, and thus their energy production, by limiting their energy metabolism largely to glycolysis, which was seen by early biochemists as primitive and inefficient.
  • the metabolic signatures of cancer cells are not passive responses to damaged mitochondria, but result from oncogene-directed metabolic reprogramming required to support anabolic growth.
  • Oncogene mutations that allow for increased and more efficient utilization of scarce nutrients present unique targets in treatment of cancer.
  • the disclosure provides compounds having any of structural formulae (la)-(le):
  • L 1 is selected from the group consisting of a bond, -C(O)-, -S-, -8(0) ⁇ -, -0-, -NR 6 -, -C(0)NR 6 -, -NR 6 C(0)-, -C(S)NR 6 -, -NR 6 C(S)-, -C(0)0-, -OC(O)-, -C(0)S-, -SC(O)-, -C(S)0-, -OC(S)-, -C(S)S-, -SC(S)-, -SCO ⁇ O-, -OSCO) ⁇ -, -S ⁇ ! ⁇ NR 6 - and
  • R 1 is selected from the group consisting of
  • each R 1 E is independently selected from oxo, optionally-substituted C C 4 alkyl, C C 4 fluoroalkyl, halogen, -CN, SF 5 , -N 3 , -C(0)R 1 F , -SR 1 F , -S ⁇ ! ⁇ R ⁇ , -OR 1 F , -(OCH 2 CH 2 0) n -R 1G in which n is 1-4,
  • each R 1 F is independently selected from H, C C 3 alkyl and C C 3
  • each R 1G is independently selected from H and C C 3 alkyl
  • L 2 is selected from the group consisting of a bond, -CH 2 -, -CH(CH 3 )- or -CH 2 CH 2 -;
  • Q is selected from the group consisting of H, -CH 2 OH, -C(0)OH, -C(0)OR 2A ,
  • each R 2A is independently selected from H and C C 3 alkyl
  • each R 2B is independently selected from H and C C 3 alkyl
  • L 3 is a bond, -C(O)-, -S-, -SCO) ⁇ -, -0-, -NR 6 -, -CH 2 -, -CH(CH 3 )(OH)- or-CH(OH)-;
  • R 3 is aryl or heteroaryl each (i) optionally substituted with a single substituent selected from -L 3C -(aryl optionally substituted with 1-5 R 3D ), -L 3C -(heteroaryl optionally substituted with 1-5 R 3D ), -L 3C -(cycloalkyl optionally substituted with 1-5
  • R 3D -L 3C -(heterocycloalkyl optionally substituted with 1-5 R 3D ) and (ii) optionally substituted with 1-5 R 3E ,
  • each L 3C is a bond, methylene
  • each R 3D is independently selected from oxo optionally-substituted C C 4 alkyl, C C 4 fluoroalkyl, halogen, -CN, SF 5 , -N 3 , -C(0)R 3F , -SR 3F , -S ⁇ ! ⁇ R ⁇ , -OR 3F , -NR 3G R 3F , -C(0)R 3F , -C(0)NR 3G R 3F , ,
  • each R 3E is independently selected from oxo, optionally-substituted C C 4 alkyl, C C 4 fluoroalkyl, halogen, -CN, SF 5 , -N 3 , -C(0)R 3F , -SR 3F , -SCC ⁇ R ⁇ , -OR 3F , -NR 3G R 3F , -C(0)R 3F , -C(0)NR 3G R 3F , ,
  • each R 3F is independently selected from H, C C 3 alkyl and C C 3
  • each R 3G is independently selected from H and C C 3 alkyl, C C 3
  • L 4 is is selected from the group consisting of a bond, -C(O)-, -S-, -8(0) ⁇ -, -0-, -NR 6 -, -C(0)NR 6 -, -NR 6 C(0)-, -C(S)NR 6 -, -NR 6 C(S)-, -C(0)0-, -0C(0)-, -C(0)S-, -SC(O)-, -C(S)0-, -OC(S)-, -C(S)S-, -SC(S)-, -SiOj L zO-, -OSCO) ⁇ -, -SCC ⁇ NR 6 - and
  • R 4 is selected from the group consisting of hydrogen, optionally substituted C C 8 alkyl, optionally-substituted C C 8 alkenyl and optionally substituted C C 8 alkynyl;
  • R 5 is aryl, heteroaryl, cycloalkyi or heterocycloalkyi, each (i) optionally substituted with a single substituent selected from -L 5C -(phenyl optionally substituted with 1-5
  • R 5D -L 5C -(monocyclic heteroaryl optionally substituted with 1-5 R 5D ),
  • each L 5C is a bond, methylene
  • each R 5D is independently selected from oxo, optionally-substituted C C 4 alkyl, C C 4 fluoroalkyl, halogen, -CN, SF 5 , -N 3 , -C(0)R 3F , -SR 3F , -S ⁇ ! ⁇ R ⁇ , -OR 3F , -NR 3G R 3F , -C(0)R 3F , -C(0)NR 3G R 3F , ,
  • each R 5E is independently selected from oxo, optionally-substituted C C 4 alkyl, C C 4 fluoroalkyl, halogen, -CN, -SF 5 , -N 3 , -C(0)R 5F , -SR 5F , -SiOj L zR 51 ", -OR 5F , -NR 5G R 5F , -C(0)R 5F , -C(0)NR 5G R 5F , -NR 5G C(0)R 5F , -C(S)NR 5G R 5F , -NR 1G C(S)R 5F , -C(0)OR 5F , -OC(0)R 5F , -C(0)SR 5F , -SC(0)R 5F , -C(S)OR 5F , -OC(S)R 5F , -C(S)SR 5F , -SC(S)OR 5F , -OC(S)R 5F
  • each R 5F is independently selected from H, C C 3 alkyl and C C 3
  • each R 5G is independently selected from H and C C 3 alkyl
  • each R 6 is selected from the group consisting of hydrogen, C C 3 alkyl and -C(0)(C C 3 alkyl);
  • each optionally substituted alkyl, alkenyl and alkynyl is unsubstituted, fluorinated or
  • each cycloalkyi has 3-10 ring carbons and is unsaturated or partially unsaturated, and optionally includes one or two fused cycloalkyi rings, each fused ring having 3-8 ring members;
  • each heterocylcloalkyl has 3-10 ring members and 1-3 heteroatoms independently
  • each aryl is a phenyl or a naphthyl, and optionally includes one or two fused cycloalkyl or heterocycloalkyl rings, each fused cycloalkyl or heterocycloalkyl ring having 4-8 ring members;
  • each heteroaryl is a 5-6 membered monocyclic heteroaryl ring having 1-4 heteroatoms independently selected from nitrogen, oxygen and sulfur or a 8-10 membered bicyclic heteroaryl having 1-5 heteroatoms independently selected from nitrogen, oxygen or sulfur, and optionally includes one or two fused cycloalkyl or heterocycloalkyl rings, each fused cycloalkyl or heterocycloalkyl ring having 4-8 ring members.
  • each and every optionally substituted alkyl, alkylene, alkenyl, alkenylene, alkynyl and alkynylene is unsubstituted or fluorinated.
  • each and every optionally substituted alkyl, alkylene, alkenyl, alkenylene, alkynyl and alkynylene is unsubstituted.
  • compositions comprising a compound as described herein.
  • the disclosure provides a method for treating a
  • hyperproliferative disorder such as cancer in a subject in need thereof.
  • the method includes administering to the subject an effective amount of a compound as described herein.
  • the disclosure provides compounds as described herein for use in treating hyperproliferative disorders such as cancer.
  • the disclosure provides the use of a compound as described herein for the preparation of a medicament for the treatment of a hyperproliferative disorder such as cancer.
  • hyperproliferative disorder is a hematopoietic cancer. In certain alternative embodiments of the disclosure, the hyperproliferative disorder is a solid tumor.
  • hyperproliferative disorder is a cancer (e.g., a solid tumor such as a colorectal cancer, a lung cancer or a pancreatic cancer) having a mutant KRAS gene, e.g., a heterozygous mutant KRAS gene.
  • a cancer e.g., a solid tumor such as a colorectal cancer, a lung cancer or a pancreatic cancer
  • a mutant KRAS gene e.g., a heterozygous mutant KRAS gene.
  • Another aspect of the disclosure provides a method for inhibiting cell cycle progression in a cancer cell.
  • the method includes contacting the cancer cell with an effective amount of a compound as described herein.
  • the cancer cell is a hematopoietic cancer cell.
  • the cancer cell is a cancer cell of a solid tumor (e.g., a pancreatic cancer, a lung cancer, or a colorectal cancer).
  • the cancer cell has a heterozygous mutant KRAS gene.
  • Cell cycle progression can be inhibited, for example, at the G0/G1 phase.
  • Another aspect of the disclosure provides a method for inducing apoptosis of a cancer cell. The method includes contacting the cancer cell with an effective amount of a compound as described herein. In certain such embodiments, the cancer cell is a hematopoietic cancer cell.
  • Another aspect of the disclosure provides a method for inducing cytotoxic effect of a cancer cell.
  • the method includes contacting the cancer cell with an effective amount of a compound as described herein.
  • the cancer cell is a hematopoietic cancer cell.
  • the cancer cell is a cancer cell of a solid tumor (e.g., a pancreatic cancer, a lung cancer, or a colorectal cancer).
  • the cancer cell has a heterozygous mutant KRAS gene.
  • Another aspect of the disclosure provides a method for inhibiting glutathione synthesis in a cancer cell.
  • the method includes contacting the cancer cell with an effective amount of a compound as described herein.
  • the cancer cell is a hematopoietic cancer cell.
  • the cancer cell is a cancer cell of a solid tumor (e.g., a pancreatic cancer, a lung cancer, or a colorectal cancer).
  • the cancer cell has a heterozygous mutant KRAS gene.
  • the compound used in the methods, compounds and uses described herein is a compound of any of the structural formulae (I) below:
  • Figure 1 is a bar graph showing responsiveness of cell lines to treatment with a test compound of the broad disclosure with respect to KRAS genotype and KRAS zygosity of the cell lines.
  • Figure 2 is a graph showing glutathione levels in three cell lines (BJAB, HCT116, and NHFL) following treatment with the test compound.
  • BJAB is represented by dark gray (bottom) line
  • HCT1 16 is represented by black (middle) line
  • NHFL is represented by light gray (top) line.
  • Figure 3 is a pair of bar graphs demonstrating reduction in glutathione levels in HCT-1 16 cells after treatment with the test compound (top) and menadione treatment (bottom), both in the presence and absence of N-acetyl cysteine (NAC).
  • Figure 4A is a set of graphs representing flow cytometry data collected from a representative cell cycle experiments in HCT116 cells after treatment with the test compound .
  • Figure 4B is a bar representation of the data in Figure 4A as the percentage of cells in each phase of the cell cycle.
  • the disclosure provides methods, compounds and uses for treating a variety of hyperproliferative disorders using a compound as described herein.
  • the compound can be defined generically as with respect to any of formulae (la), (lb), (Ic) and (Id) above, or in various subgenera compounds in which the structural formula, R 1 , L 1 , L 2 , Q, L 3 , R 3 , L 4 , R 4 , L 5 , and R 5 are optionally independently selected from the groups (la) et seq., (1a) et seq., (2a) et seq., (3a) et seq., (4a) et seq., (5a) et seq., (6a) et seq., (7a) et seq., (8a) et seq., (9a) et seq., and (10a) et seq., defined hereinbelow (e.g., wherein the compound is of
  • the compound has one of the following structural formulae:
  • R 1 is selected from one of the following groups (1a) - (1 k):
  • R 1 is selected from the group consisting of hydrogen, optionally substituted C C 8 alkyl and cycloalkyl optionally substituted with 1-5 R 1 E ;
  • R 1 is optionally substituted C C 8 alkyl
  • R 1 is unsubstituted C C 8 alkyl or fluorinated C C 8 alkyl, e.g., propyl or butyl;
  • R 1 is unsubstituted cycloalkyl
  • R 1 is optionally substituted C C 8 alkenyl
  • R 1 is phenyl optionally substituted with 1-5 R E ;
  • R 1 is propyl, butyl, or butenyl
  • R 1 is trifluoromethyl-substituted phenyl, methoxy-substituted phenyl or fluoro- substituted phenyl.
  • R 1 is phenyl substituted with -(OCH 2 CH 2 0)n-R 1G in which n is 1-4,
  • each optionally substituted alkyl of R 1 (including those of R 1 E ) is unsubstituted or fluorinated.
  • each optionally substituted alkyl, alkenyl and alkynyl of R 1 (including those of R 1 E ) is unsubstituted.
  • L 1 is selected from one of the following groups (2a) - (2e)
  • L 1 is a bond, -S-, -S(O)- or -S(0) 2 -;
  • L 1 is selected from a bond, -CH 2 -, -CH(CH 3 )-, -CH 2 CH 2 -, -C(O)-, -S-, -S O) ⁇ -, -0-, and -NR 6 -;
  • L 1 is -O- or -S-.
  • L 1 is a bond (e.g., when R 1 is (1d), (1f), (1g), (1 i), (1j) or (1 k) above);
  • L 2 is selected from one of the following groups (3a) - (3c)
  • L 2 is -CH 2 -, -CH(CH 3 )- or -CH 2 CH 2 -;
  • L 2 is a bond or -CH 2 -.
  • Q is selected from one of the following groups (4a) - (4d)
  • Q is selected from the group consisting of -CH 2 OH, -C(0)OH, -C(0)OR 2A ,
  • Q is selected from the group consisting of -CH 2 OH, -C(0)OH, -C(0)OR 2A ,
  • Q is -CH 2 OH, -C(0)OH or -C(0)OR 2A ;
  • L 3 is selected from one of the following groups (5a) - (5c)
  • L 3 is a bond, -C(O)-, -S-, -SOD) ⁇ -, -0-, -NR 6 -, -CH 2 -, -CH(CH 3 )(OH)- or -CH(OH)-;
  • L 3 is a bond, -CH 2 -, -CH(CH 3 )(OH)- or -CH(OH)-. [30] In certain embodiments of the compounds as otherwise described herein, R 3 is selected from one of the following groups (6a) - (6k)
  • R 3 is aryl (e.g., phenyl) or heteroaryl (e.g., monocyclic heteroaryl) each (i) optionally substituted with a single substituent selected from -L 3C -(aryl optionally substituted with 1-5 R 3D ), -L 3C -(heteroaryl optionally substituted with 1-5 R 3D ), -L 3C -(cycloalkyl optionally substituted with 1-5 R 3D ), -L 3C -(heterocycloalkyl optionally substituted with 1-5 R 3D ) and (ii) optionally substituted with 1-5 R 3E ;
  • aryl e.g., phenyl
  • heteroaryl e.g., monocyclic heteroaryl
  • R 3 is aryl (e.g., a phenyl, a benzodioxole, or a dihydro-1 H-isoquinoline) optionally substituted with 1-5 R 3E ;
  • R 3 is aryl (e.g., a phenyl, a benzodioxole, or a dihydro-1 H-isoquinoline) (i)
  • R 3 is aryl (e.g., a phenyl, a benzodioxole, or a dihydro-1 H-isoquinoline) (i)
  • R 3D -L 3C -(monocyclic heterocycloalkyl optionally substituted with 1-5 R 3D ) and (ii) optionally substituted with 1-5 R 3E ;
  • R 3 is as defined in (6a)-(6d), wherein the aryl is not substituted with any R 3E ;
  • R 3 is heteroaryl (e.g., an isothiazole, a pyridone, a thiadiazole, a pyrazine, a
  • pyrazolopyrimidine a pyrazolopyridine, an imidazole, a benzofuran, an indole, an imidazopyridine, a pyridine, a pyrazole, an isoxazole, a triazolopyridine, a benzimidazole, a thiophene, a benzothiophene, a furan or a pyrimidine) optionally substituted with 1-5 R 3E ;
  • R 3 is heteroaryl (e.g., an isothiazole, a pyridone, a thiadiazole, a pyrazine, a
  • pyrazolopyrimidine a pyrazolopyridine, an imidazole, a benzofuran, an indole, an imidazopyridine, a pyridine, a pyrazole, an isoxazole, a triazolopyridine, a benzimidazole, a thiophene, a benzothiophene, a furan or a pyrimidine) (i) substituted with a single substituent selected from -L 3C -(aryl optionally substituted with 1-5 R 3D ), -L 3C -(heteroaryl optionally substituted with 1-5 R 3D ), -L 3C -(cycloalkyl optionally substituted with 1-5 R 3D ), -L 3C -(heterocycloalkyl optionally substituted with 1-5 R 3D ) and (ii) optionally substituted with 1-5 R 3E ;
  • R 3 is heteroaryl (e.g., an isothiazole, a pyridone, a thiadiazole, a pyrazine, a
  • pyrazolopyrimidine a pyrazolopyridine, an imidazole, a benzofuran, an indole, an imidazopyridine, a pyridine, a pyrazole, an isoxazole, a triazolopyridine, a benzimidazole, a thiophene, a benzothiophene, a furan or a pyrimidine) (i) substituted with a single substituent selected from -L 3C -(phenyl optionally substituted with 1 -5 R 3D ), -L 3C -(monocyclic heteroaryl optionally substituted with 1 -5 R 3D ), -L 3C -(monocyclic cycloalkyl optionally substituted with 1-5
  • R 3D -L 3C -(monocyclic heterocycloalkyl optionally substituted with 1 -5 R 3D ) and (ii) optionally substituted with 1-5 R 3E ;
  • R 3 is as defined in (6f)-(6h), wherein the heteroaryl is not substituted with any R 3E ;
  • R 3 is selected from the group consisting of: phenyl, benzodioxolyl, dihydro-1 H- isoquinolinyl, imidazolyl, oxazolyl, isoxazolyl, isothiazolyl, thiazolyl, pyridinyl, and pyrazinyl, pyridonyl, thiadiazolyl, pyrazolopyrimidinyl, pyrazolopyridinyl,
  • R 3D -L 3C -(cycloalkyl optionally substituted with 1 -5 R 3D ), -L 3C -(heterocycloalkyl optionally substituted with 1-5 R 3D ) and (ii) optionally substituted with 1 -5 R 3E .
  • R 3 is selected from the group consisting of phenyl and monocyclic heteroaryl (e.g. , pyridyl, pyrazolyl), optionally substituted with 1 -5 R 3E .
  • each optionally substituted alkyl, alkenyl and alkynyl of R 3 is unsubstituted or fluorinated.
  • each optionally substituted alkyl, alkenyl and alkynyl of R 3 is unsubstituted.
  • L 3C is methylene or -O-.
  • the optional number of R3E substituents is 1-3, or 1 -2.
  • R 4 is selected from one of the following groups (7a) - (7d)
  • R 4 is hydrogen
  • R 4 is optionally substituted C C 8 alkyl, optionally-substituted C C 8 alkenyl or optionally substituted C C 8 alkynyl;
  • R 4 is hydrogen or unsubstituted C C 6 alkyl
  • R 4 is unsubstituted C C 3 alkyl.
  • each optionally substituted alkyl, alkenyl and alkynyl of R 4 is unsubstituted or fluorinated.
  • each optionally substituted alkyl, alkenyl and alkynyl of R 4 is unsubstituted.
  • L 4 is selected from one of the following groups (8a) - (8c)
  • L 4 is selected from a bond, -C(O)-, -S-, -S(0)i. 2 -, -0-, and -NR 6 -; (8b) L 4 is a bond;
  • L 4 is -O- (e.g., when R 4 is any of (7a), (7b), (7c) or (7d) above).
  • L 5 is selected from one of the following groups (9a) - (9c)
  • L 5 is a bond, -C(O)-, -S-, -SiO) ⁇ -, -0-, -NR 6 -, -CH 2 CH 2 -, -CH 2 -, -CH(CH 3 )(OH)- or -CH(OH)-;
  • L 5 is a bond, -0-, -S-, -C(O)- or -S(0) 1-2 -.
  • R 5 is selected from one of the following groups (21 o) - (21 g)
  • R 5 is aryl (e.g., phenyl) or heteroaryl (e.g., an isoxazolyl, a pyridyl, an
  • R 5 is phenyl optionally substituted with 1-5 R 5E ;
  • R 5 is selected from the group consisting of phenyl, isoxazolyl, pyridyl,
  • R 5 is phenyl substituted with a single substituent selected from -L 5C -(phenyl optionally substituted with 1-5 R 5D ), -L 5C -(monocyclic heteroaryl optionally substituted with 1-5 R 5D ), and -L 5C -(monocyclic cycloalkyl optionally substituted with 1-5 R 5D ) -L 5C -(monocyclic heterocycloalkyl optionally substituted with 1-5
  • R 5D and (ii) optionally substituted with 1-5 R 5E ;
  • R 5 is phenyl substituted with a single -L 5C -(monocyclic heteroaryl optionally
  • R 5 is phenyl substituted with a single -L 5C -(monocyclic heterocycloalkyl optionally substituted with 1-5 R 5D ) substiuent and (ii) optionally substituted with 1-5 R 5E ;
  • R 5 is phenyl substituted with a single -L 5C -(monocyclic heterocycloalkyl optionally substituted with 1-5 R 5D ) substiuent and (ii) optionally substituted with 1-5 R 5E ;
  • R 5 is heterocycloalkyl optionally substituted with 1-5 R 5E ;
  • R 5 is heterocycloalkyl substituted with a single -L 5C -(monocyclic cycloalkyl
  • heterocycloalkyl attached to the -L 5 - through a nitrogen atom
  • R 5 is cycloalkyl optionally substituted with 1-5 R 5E ; (10o) (10n) above, in which the cycloalkyl is substituted with 1-5 R ;
  • each optionally substituted alkyl, alkenyl and alkynyl of R 5 (including those of R 5D and R 5E ) is unsubstituted or fluorinated.
  • each optionally substituted alkyl, alkenyl and alkynyl of R 5 (including those of R 5D and R 5E ) is unsubstituted.

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  • Chemical Kinetics & Catalysis (AREA)
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CN201780084999.4A CN110603254B (zh) 2016-11-30 2017-11-29 被取代的吡唑化合物以及使用其治疗过度增生性疾病的方法
CN202410345199.5A CN118930533A (zh) 2016-11-30 2017-11-29 被取代的吡唑化合物以及使用其治疗过度增生性疾病的方法
JP2019528861A JP7373992B2 (ja) 2016-11-30 2017-11-29 過剰増殖性疾患の治療のための置換ピラゾール化合物およびそれらの使用方法
MX2019006299A MX2019006299A (es) 2016-11-30 2017-11-29 Compuestos de pirazola sustituida y metodos para usarlos para el tratamiento de enfermedades hiperproliferativas.
BR112019011044-5A BR112019011044A2 (pt) 2016-11-30 2017-11-29 compostos pirazol substituídos e métodos de uso no tratamento de doenças hiperproliferativas
EP17876486.6A EP3548482A4 (en) 2016-11-30 2017-11-29 SUBSTITUTED PYRAZOLE COMPOUNDS AND THEIR METHODS OF USE FOR THE TREATMENT OF HYPERPROLIFERATIVE DISEASES
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US12398154B2 (en) 2020-12-15 2025-08-26 Mirati Therapeutics, Inc. Azaquinazoline pan-KRas inhibitors
US12421253B2 (en) 2020-12-16 2025-09-23 Mirati Therapeutics, Inc. Tetrahydropyridopyrimidine pan-KRas inhibitors
US12485122B2 (en) 2018-09-10 2025-12-02 Mirati Therapeutics, Inc. Combination of palbociclib and adagrasib for lung cancer
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US10633381B2 (en) 2016-05-18 2020-04-28 Mirati Therapeutics, Inc. KRas G12C inhibitors
US10647715B2 (en) 2017-11-15 2020-05-12 Mirati Therapeutics, Inc. KRas G12C inhibitors
US10689377B2 (en) 2017-11-15 2020-06-23 Mirati Therapeutics, Inc. KRas G12C inhibitors
US11932633B2 (en) 2018-05-07 2024-03-19 Mirati Therapeutics, Inc. KRas G12C inhibitors
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US12208099B2 (en) 2018-09-10 2025-01-28 Mirati Therapeutics, Inc. Combination therapies
US12485122B2 (en) 2018-09-10 2025-12-02 Mirati Therapeutics, Inc. Combination of palbociclib and adagrasib for lung cancer
US12377101B2 (en) 2018-12-05 2025-08-05 Mirati Therapeutics, Inc. Combination therapies
US11548888B2 (en) 2019-01-10 2023-01-10 Mirati Therapeutics, Inc. KRas G12C inhibitors
JP2022535228A (ja) * 2019-05-31 2022-08-05 バンタム、ファーマシューティカル、リミテッド、ライアビリティー、カンパニー チアゾリルピラゾールカルボン酸の製造方法およびそれらのための中間体
CN114901655A (zh) * 2019-05-31 2022-08-12 班塔姆制药有限责任公司 1-噻唑-2-基-吡唑-5-甲酸衍生物的结晶多晶型物
CN114867724A (zh) * 2019-05-31 2022-08-05 班塔姆制药有限责任公司 用于制备噻唑基吡唑甲酸及其中间体的方法
CN114867724B (zh) * 2019-05-31 2025-11-07 班塔姆制药有限责任公司 用于制备噻唑基吡唑甲酸及其中间体的方法
US12378234B2 (en) 2019-05-31 2025-08-05 Bantam Pharmaceutical, Llc Crystalline polymorphs of a 1-thiazol-2-yl-pyrazole-5-carboxylic acid derivative
JP2022534429A (ja) * 2019-05-31 2022-07-29 バンタム、ファーマシューティカル、リミテッド、ライアビリティー、カンパニー １－チアゾール－２－イル－ピラゾール－５－カルボン酸誘導体の結晶多形
WO2020243582A1 (en) 2019-05-31 2020-12-03 Bantam Pharmaceutical, Llc Methods for making thiszolylpyrazole carboxylic acids and intermediates therefor
WO2020243584A1 (en) 2019-05-31 2020-12-03 Bantam Pharmaceutical, Llc Crystalline polymorphs of a 1-thiazol-2-yl-pyrazole-5-carboxylic acid derivative
US11453683B1 (en) 2019-08-29 2022-09-27 Mirati Therapeutics, Inc. KRas G12D inhibitors
US11964989B2 (en) 2019-08-29 2024-04-23 Mirati Therapeutics, Inc. KRas G12D inhibitors
US11890285B2 (en) 2019-09-24 2024-02-06 Mirati Therapeutics, Inc. Combination therapies
US11702418B2 (en) 2019-12-20 2023-07-18 Mirati Therapeutics, Inc. SOS1 inhibitors
US12304915B2 (en) 2019-12-20 2025-05-20 Mirati Therapeutics, Inc. SOS1 inhibitors
WO2021245055A1 (en) * 2020-06-02 2021-12-09 Boehringer Ingelheim International Gmbh Annulated 2-amino-3-cyano thiophenes and derivatives for the treatment of cancer
US11945812B2 (en) 2020-06-02 2024-04-02 Boehringer Ingelheim International Gmbh Annulated 2-amino-3-cyano thiophenes and derivatives for the treatment of cancer
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US12545670B2 (en) 2020-06-02 2026-02-10 Boehringer Ingelheim International Gmbh Annulated 2-amino-3-cyano thiophenes and derivatives for the treatment of cancer
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US12281113B2 (en) 2020-09-11 2025-04-22 Mirati Therapeutics, Inc. Crystalline forms of a KRas G12C inhibitor
US12398154B2 (en) 2020-12-15 2025-08-26 Mirati Therapeutics, Inc. Azaquinazoline pan-KRas inhibitors
US12421253B2 (en) 2020-12-16 2025-09-23 Mirati Therapeutics, Inc. Tetrahydropyridopyrimidine pan-KRas inhibitors
US12060367B2 (en) 2021-12-01 2024-08-13 Boehringer Ingelheim International Gmbh Annulated 2-amino-3-cyano thiophenes and derivatives for the treatment of cancer
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