US20170050958A1 - Cycloalkyl-Linked Diheterocycle Derivatives - Google Patents

Cycloalkyl-Linked Diheterocycle Derivatives Download PDF

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Publication number
US20170050958A1
US20170050958A1 US15/306,979 US201515306979A US2017050958A1 US 20170050958 A1 US20170050958 A1 US 20170050958A1 US 201515306979 A US201515306979 A US 201515306979A US 2017050958 A1 US2017050958 A1 US 2017050958A1
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Prior art keywords
membered heteroaryl
compound
cycloalkyl
alkyl
optionally substituted
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US15/306,979
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Inventor
Aaron Craig BURNS
Michael Raymond Collins
Samantha Elizabeth Greasley
Robert Louis Hoffman
Peter Qinhua HUANG
Robert Steven Kania
Pei-Pei Kung
Maria Angelica Linton
Lakshmi Sourirajan Narasimhan
Paul Francis Richardson
Daniel Tyler Richter
Graham Smith
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Pfizer Corp SRL
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Pfizer Corp SRL
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Priority to US15/306,979 priority Critical patent/US20170050958A1/en
Publication of US20170050958A1 publication Critical patent/US20170050958A1/en
Priority to US15/826,027 priority patent/US10125130B2/en
Abandoned legal-status Critical Current

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    • 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
    • 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
    • C07D417/08—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 linked by a carbon chain containing alicyclic 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
    • A61K31/433—Thidiazoles
    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
    • C07D285/01—Five-membered rings
    • C07D285/02—Thiadiazoles; Hydrogenated thiadiazoles
    • C07D285/04—Thiadiazoles; Hydrogenated thiadiazoles not condensed with other rings
    • C07D285/12—1,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles
    • C07D285/125—1,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical
    • C07D285/135—Nitrogen atoms
    • 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
    • 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
    • A61K31/435—Heterocyclic 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
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • 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
    • A61K31/435—Heterocyclic 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
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
    • 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
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/50—Pyridazines; Hydrogenated pyridazines
    • A61K31/501—Pyridazines; Hydrogenated pyridazines not condensed and containing further heterocyclic 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
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three 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
    • C07D277/38—Nitrogen atoms
    • C07D277/44—Acylated amino or imino radicals
    • C07D277/46—Acylated amino or imino radicals by carboxylic acids, or sulfur or nitrogen analogues thereof
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings

Definitions

  • the present invention relates to novel cycloalkyl-linked diheterocycle derivatives that are useful in the treatment of abnormal cell growth, such as cancer, in mammals.
  • the present invention also relates to pharmaceutical compositions containing the compounds and to methods of using the compounds and compositions in the treatment of abnormal cell growth in mammals.
  • Tumor cells require nutrients to generate ATP and macromolecules to sustain survival and proliferation.
  • Glucose and glutamine are two major sources of nutrients that tumor cells depend on. Tumor cells prefer to use glycolysis pathways, even under aerobic conditions, to metabolize glucose to produce lactic acid and ATP, the so-called Warburg's effect.
  • Gln glutamine
  • Gin metabolism in cancer cells is regulated and cross-talks with multiple oncogenic pathways (Gao P, et al., “c-Myc Suppression of miR-23a/b Enhances Mitochondrial Glutaminase Expression and Glutamine Metabolism”, Nature. 458(7239) (2009), pp. 762-5; Durán R V, et al. “Glutaminolysis Activates Rag-mTORC1 Signaling”, Mol Cell. 47(3) (2012), pp.
  • Glutamate is also the critical substrate for glutathione synthesis, which plays important role in redox homeostasis.
  • GLS1 is overexpressed across many tumor types, and myc up-regulates GLS1 protein level through transcriptional repression of miR-23a and miR-23b. Suppression of GLS1 with selective small molecule inhibitors may be valuable to treat different types of cancers (Wise D. R., et al., “Glutamine Addiction: a New Therapeutic Target in Cancer”, Trends Biochem Sci. 35(8) 2010, pp.
  • Embodiments described herein relate to a compound of formula (I)
  • a and D are independently 5 or 6-membered heteroaryl optionally substituted by one or two R 7 groups;
  • L is —(C 4 -C 10 cycloalkyl)- optionally substituted by one to three substituents selected from the group consisting of halogen, cyano, C 1 -C 4 alkyl, hydroxy, and C 1 -C 4 alkoxy;
  • R 1 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10a , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups;
  • R 2 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups;
  • R 3 , R 4 , R 5 and R 6 are each independently hydrogen, halogen, C 1 -C 4 alkyl, C 1 -C 4 alkoxy or C 3 -C 6 cycloalkyl;
  • each R 7 is each independently hydrogen, halogen, cyano, C 1 -C 2 alkyl, hydroxy, C 1 -C 2 alkoxy, or —N(R 11 )(R 12 ), wherein the C 1 -C 2 alkyl and the C 1 -C 2 alkoxy are each independently optionally substituted by halogen or hydroxy;
  • R 10a and R 10b are each independently hydrogen, C 1 -C 4 alkyl, —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl), wherein the C 1 -C 4 alkyl, the C 4 -C 10 cycloalkyl, the 4-6 membered heterocycloalkyl, the C 6 -C 10 aryl, and the 5-10 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one, two or three halogen, cyano, C 1 -C 6 alkyl, hydroxy, C 1 -C
  • each R 11 , R 12 , R 13 , R 14 and R 15 is independently hydrogen, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, C 3 -C 6 cycloalkyl, or 3-6 membered heterocycloalkyl, wherein the C 1 -C 4 alkyl, the C 3 -C 6 cycloalkyl, and the 3-6 membered heterocycloalkyl are each independently optionally substituted by one, two or three substituents selected from the group consisting of halogen, cyano, hydroxy, and methoxy;
  • w 0, 1, 2 or 3;
  • x is 0 or 1
  • y is 0 or 1, provided that at least one of x and y is 0;
  • z 0, 1, 2 or 3;
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein A and D are independently thiadiazolyl, pyridazinyl optionally substituted by one or two R 7 groups, and 1,2,4-triazinyl optionally substituted by R 7 .
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein at least one of A and D is
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein y is 0.
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein D is
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein A is pyridazinyl optionally substituted by one or two R 7 groups.
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein A is
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein x is 0 and y is 0 or 1.
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein x is 1 and y is 0.
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein L is
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein L is
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein
  • R 1 is —C(O)R 10a and R 2 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 2 is —C(O)R 10b and R 2 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)Rb, or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein R 10a is C 1 -C 4 alkyl and R 10b is C 1 -C 4 alkyl.
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the C 6 aryl and the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two halogen or C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein at least one of R 1 and R 2 is C 1 -C 4 alkyl.
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein R 1 and R 2 each independently C 1 -C 4 alkyl.
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein at least one of R 1 and R 2 is hydrogen.
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein at least one of R 1 and R 2 is C 3 -C 6 cycloalkyl optionally substituted by one or two R 15 groups.
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein at least one of R 1 and R 2 is 5-6 membered heteroaryl optionally substituted by one or two R 15 groups.
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein L is
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein
  • R 1 is —C(O)R 10a and R 2 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 2 is —C(O)R 10b and R 1 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z (C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z (C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 6 aryl), or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the C 6 aryl and the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two halogen or C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the aryl and the heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein each R 13 and R 14 is hydrogen and each z is 1.
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyridinyl and R 10b is —CH 2 -pyridinyl, wherein each pyridinyl is optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyridinyl optionally substituted by one or two C 1 -C 4 alkyl groups and R 10b is —CH 2 -pyrazolyl optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z (C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the C 6 aryl and the 5-6 membered heteroaryl in R 10a are each independently optionally substituted by one or two halogen or C 1 -C 4 alkyl groups, and R 10b is C 1 -C 4 alkyl optionally substituted by C 1 -C 6 alkoxy.
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein each R 13 and R 14 is hydrogen and each z is 1.
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein R 10a is —(CH 2 )-(5-6 membered heteroaryl) optionally substituted by one or two C 1 -C 4 alkyl groups and R 10b is C 1 -C 4 alkyl optionally substituted by C 1 -C 2 alkoxy.
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyridinyl and R 10b is —CH 2 CH 2 —O—CH 3 .
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein R 1 is —C(O)R 10a and R 2 is C 3 -C 6 cycloalkyl optionally substituted by one or two R 15 groups.
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein each R 13 and R 14 is hydrogen and each z is 1.
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -(5-6 membered heteroaryl) optionally substituted by one or two halogen or C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyridinyl optionally substituted by one or two C 1 -C 4 alkyl groups and R 2 is cyclopropyl.
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein L is
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein
  • R 1 is —C(O)R 10a and R 2 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 2 is —C(O)R 10b and R 1 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 6 aryl) or -[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the C 6 aryl and the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two halogen or C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) optionally substituted by one or two C 1 -C 4 alkyl groups and R 10b is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyrazolyl optionally substituted by one or two C 1 -C 4 alkyl groups and R 10b is —CH 2 -pyrazolyl optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein L is
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein
  • R 1 is —C(O)R 10a and R 2 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 2 is —C(O)R 10b and R 1 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )]—(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z -(6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the C 6 aryl and the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two halogen or C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein each R 13 and R 14 is hydrogen and each z is 1.
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyridinyl optionally substituted by one or two C 1 -C 4 alkyl groups and R 10b is —CH 2 -pyridinyl optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein L is
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein
  • R 1 is —C(O)R 10a and R 2 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 2 is —C(O)R 10b and R 1 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 6 aryl), or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the C 6 aryl and the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two halogen or C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein each R 13 and R 14 is hydrogen and each z is 1.
  • Embodiments described herein relate to a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyridinyl optionally substituted by one or two C 1 -C 4 alkyl groups and R 10b is —CH 2 -pyridinyl optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (II)
  • a and D are independently
  • L is —(C 4 -C 10 cycloalkyl)- optionally substituted by one to three substituents selected from the group consisting of halogen, cyano, C 1 -C 4 alkyl, hydroxy, and C 1 -C 4 alkoxy;
  • R 1 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10a , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups;
  • R 2 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups;
  • R 3 , R 4 , R 5 and R 6 are each independently hydrogen, halogen, C 1 -C 4 alkyl, C 1 -C 4 alkoxy or C 3 -C 6 cycloalkyl;
  • R 7 , R 8 and R 9 are each independently hydrogen, halogen, cyano, C 1 -C 2 alkyl, hydroxy, C 1 -C 2 alkoxy, or —N(R 11 )(R 12 ), wherein the C 1 -C 2 alkyl and the C 1 -C 2 alkoxy are each independently optionally substituted by halogen or hydroxy;
  • R 10a and R 10b are each independently hydrogen, C 1 -C 4 alkyl, —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl), wherein the C 1 -C 4 alkyl, the C 4 -C 10 cycloalkyl, the 4-6 membered heterocycloalkyl, the C 6 -C 10 aryl, and the 5-10 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one, two or three halogen, cyano, C 1 -C 6 alkyl, hydroxy, C 1 -C
  • w 0, 1, 2 or 3;
  • x is 0 or 1
  • y is 0 or 1, provided that at least one of x and y is 0;
  • z 0, 1, 2 or 3;
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein y is 0.
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein D is
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein A is
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein A is
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein x is 0 and y is 0 or 1.
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein x is 1 and y is 0.
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein L is
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein L is
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein
  • R 1 is —C(O)R 10a and R 2 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 2 is —C(O)R 10b and R 1 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein R 10a is C 1 -C 4 alkyl and R 10b is C 1 -C 4 alkyl.
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 ary
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z (C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the C 6 aryl and the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two halogen or C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein at least one of R 1 and R 2 is C 1 -C 4 alkyl.
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein R 1 and R 2 each independently C 1 -C 4 alkyl.
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein at least one of R 1 and R 2 is hydrogen.
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein at least one of R 1 and R 2 is C 3 -C 6 cycloalkyl optionally substituted by one or two R 15 groups.
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein at least one of R 1 and R 2 is 5-6 membered heteroaryl optionally substituted by one or two R 15 groups.
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein L is
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein
  • R 1 is —C(O)R 10a and R 2 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 2 is —C(O)R 10b and R 1 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z (C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl),
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )]—(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 6 aryl), or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the C 6 aryl and the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two halogen or C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the aryl and the heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein each R 13 and R 14 is hydrogen and each z is 1.
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyridinyl and R 10b is —CH 2 -pyridinyl, wherein each pyridinyl is optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyridinyl optionally substituted by one or two C 1 -C 4 alkyl groups and R 10b is —CH 2 -pyrazolyl optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 ary
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein is —[C(R 13 )(R 14 )] z -(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the C 6 aryl and the 5-6 membered heteroaryl in R 10a are each independently optionally substituted by one or two halogen or C 1 -C 4 alkyl groups, and R 10b is C 1 -C 4 alkyl optionally substituted by C 1 -C 6 alkoxy.
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein each R 13 and R 14 is hydrogen and each z is 1.
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein R 10a is —(CH 2 )-(5-6 membered heteroaryl) optionally substituted by one or two C 1 -C 4 alkyl groups and R 10b is C 1 -C 4 alkyl optionally substituted by C 1 -C 2 alkoxy.
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyridinyl and R 10b is —CH 2 CH 2 —O—CH 3 .
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein R 1 is —C(O)R 10a and R 2 is C 3 -C 6 cycloalkyl optionally substituted by one or two R 15 groups.
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 ary
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein each R 13 and R 14 is hydrogen and each z is 1.
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -(5-6 membered heteroaryl) optionally substituted by one or two halogen or C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyridinyl optionally substituted by one or two C 1 -C 4 alkyl groups and R 2 is cyclopropyl.
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein L is
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein
  • R 1 is —C(O)R 10a and R 2 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 2 is —C(O)R 10b and R 1 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein R 1 is —C(O)R 10a and R 2 is —C(O)R 1b
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z (C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z (4-10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )]—(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the C 6 aryl and the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two halogen or C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) optionally substituted by one or two C 1 -C 4 alkyl groups and R 10b is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyrazolyl optionally substituted by one or two C 1 -C 4 alkyl groups and R 10b is —CH 2 -pyrazolyl optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein L is
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein
  • R 1 is —C(O)R 10a and R 2 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 2 is —C(O)R 10b and R 1 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 ary
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z (C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the C 6 aryl and the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two halogen or C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein each R 13 and R 14 is hydrogen and each z is 1.
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyridinyl optionally substituted by one or two C 1 -C 4 alkyl groups and R 10b is —CH 2 -pyridinyl optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein, wherein L is
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein
  • R 1 is —C(O)R 10a and R 2 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 2 is —C(O)R 10b and R 1 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 ary
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 6 aryl), or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the C 6 aryl and the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two halogen or C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein each R 13 and R 14 is hydrogen and each z is 1.
  • Embodiments described herein relate to a compound of formula (II), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyridinyl optionally substituted by one or two C 1 -C 4 alkyl groups and R 10b is —CH 2 -pyridinyl optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (III)
  • a and D are independently
  • L is —(C 4 -C 10 cycloalkyl)- optionally substituted by one to three substituents selected from the group consisting of halogen, cyano, C 1 -C 4 alkyl, hydroxy, and C 1 -C 4 alkoxy;
  • R 1 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10a , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups;
  • R 2 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups;
  • R 3 and R 4 are each independently hydrogen, halogen, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, or C 3 -C 6 cycloalkyl;
  • R 7 , R 8 and R 9 are each independently hydrogen, halogen, cyano, C 1 -C 2 alkyl, hydroxy, C 1 -C 2 alkoxy, or —N(R 11 )(R 12 ), wherein the C 1 -C 2 alkyl and the C 1 -C 2 alkoxy are each independently optionally substituted by halogen or hydroxy;
  • R 10a and R 10b are each independently hydrogen, C 1 -C 4 alkyl, —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl), wherein the C 1 -C 4 alkyl, the C 4 -C 10 cycloalkyl, the 4-6 membered heterocycloalkyl, the C 6 -C 10 aryl, and the 5-10 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one, two or three halogen, cyano, C 1 -C 6 alkyl, hydroxy, C 1 -C
  • each R 11 , R 12 , R 13 , R 14 and R 15 is independently hydrogen, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, C 3 -C 6 cycloalkyl, or 3-6 membered heterocycloalkyl, wherein the C 1 -C 4 alkyl, the C 3 -C 6 cycloalkyl, and the 3-6 membered heterocycloalkyl are each independently optionally substituted by one, two or three substituents selected from the group consisting of halogen, cyano, hydroxy, and methoxy;
  • w 0, 1, 2 or 3;
  • x is 0 or 1
  • z 0, 1, 2 or 3;
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein D is
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein A is
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein A is
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein x is 0.
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein x is 1.
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein L is
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein L is
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein
  • R 1 is —C(O)R 10a and R 2 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 2 is —C(O)R 10b and R 1 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein R 10a is C 1 -C 4 alkyl and R 10b is C 1 -C 4 alkyl.
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the C 6 aryl and the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two halogen or C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein at least one of R 1 and R 2 is C 1 -C 4 alkyl.
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein R 1 and R 2 each independently C 1 -C 4 alkyl.
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein at least one of R 1 and R 2 is hydrogen.
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein at least one of R 1 and R 2 is C 3 -C 6 cycloalkyl optionally substituted by one or two R 15 groups.
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein at least one of R 1 and R 2 is 5-6 membered heteroaryl optionally substituted by one or two R 15 groups.
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein L is
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein
  • R 1 is —C(O)R 10a and R 2 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 2 is —C(O)R 10b and R 1 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )]—(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 6 aryl), or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the C 6 aryl and the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two halogen or C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the aryl and the heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein each R 13 and R 14 is hydrogen and each z is 1.
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyridinyl and R 10b is —CH 2 -pyridinyl, wherein each pyridinyl is optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyridinyl optionally substituted by one or two C 1 -C 4 alkyl groups and R 10b is —CH 2 -pyrazolyl optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )]—(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the C 6 aryl and the 5-6 membered heteroaryl in R 10a are each independently optionally substituted by one or two halogen or C 1 -C 4 alkyl groups, and R 10b is C 1 -C 4 alkyl optionally substituted by C 1 -C 6 alkoxy.
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein each R 13 and R 14 is hydrogen and each z is 1.
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein R 10a is —(CH 2 )-(5-6 membered heteroaryl) optionally substituted by one or two C 1 -C 4 alkyl groups and R 10b is C 1 -C 4 alkyl optionally substituted by C 1 -C 2 alkoxy.
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyridinyl and R 10b is —CH 2 CH 2 —O—CH 3 .
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein R 1 is —C(O)R 10a and R 2 is C 3 -C 6 cycloalkyl optionally substituted by one or two R 15 groups.
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein each R 13 and R 14 is hydrogen and each z is 1.
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -(5-6 membered heteroaryl) optionally substituted by one or two halogen or C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyridinyl optionally substituted by one or two C 1 -C 4 alkyl groups and R 2 is cyclopropyl.
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein L is
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein
  • R 1 is —C(O)R 10a and R 2 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 2 is —C(O)R 10b and R 1 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )]—(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z -(6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the C 6 aryl and the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two halogen or C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) optionally substituted by one or two C 1 -C 4 alkyl groups and R 10b is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyrazolyl optionally substituted by one or two C 1 -C 4 alkyl groups and R 10b is —CH 2 -pyrazolyl optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein L is
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein
  • R 1 is —C(O)R 10a and R 2 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 2 is —C(O)R 10b and R 1 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the C 6 aryl and the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two halogen or C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein each R 13 and R 14 is hydrogen and each z is 1.
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyridinyl optionally substituted by one or two C 1 -C 4 alkyl groups and R 10b is —CH 2 -pyridinyl optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein, wherein L is
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein
  • R 1 is —C(O)R 10a and R 2 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 2 is —C(O)R 10b and R 1 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 6 aryl), or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the C 6 aryl and the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two halogen or C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein each R 13 and R 14 is hydrogen and each z is 1.
  • Embodiments described herein relate to a compound of formula (III), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyridinyl optionally substituted by one or two C 1 -C 4 alkyl groups and R 10b is —CH 2 -pyridinyl optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IV)
  • L is —(C 4 -C 10 cycloalkyl)- optionally substituted by one to three substituents selected from the group consisting of halogen, cyano, C 1 -C 4 alkyl, hydroxy, and C 1 -C 4 alkoxy;
  • R 1 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10a , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups;
  • R 2 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups;
  • R 3 and R 4 are each independently hydrogen, halogen, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, or C 3 -C 6 cycloalkyl;
  • R 7 , R 8 and R 9 are each independently hydrogen, halogen, cyano, C 1 -C 2 alkyl, hydroxy, C 1 -C 2 alkoxy, or —N(R 11 )(R 12 ), wherein the C 1 -C 2 alkyl and the C 1 -C 2 alkoxy are each independently optionally substituted by halogen or hydroxy;
  • R 10a and R 10b are each independently hydrogen, C 1 -C 4 alkyl, —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl), wherein the C 1 -C 4 alkyl, the C 4 -C 10 cycloalkyl, the 4-6 membered heterocycloalkyl, the C 6 -C 10 aryl, and the 5-10 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one, two or three halogen, cyano, C 1 -C 6 alkyl, hydroxy, C 1 -C
  • each R 11 , R 12 , R 13 , R 14 and R 15 is independently hydrogen, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, C 3 -C 6 cycloalkyl, or 3-6 membered heterocycloalkyl, wherein the C 1 -C 4 alkyl, the C 3 -C 6 cycloalkyl, and the 3-6 membered heterocycloalkyl are each independently optionally substituted by one, two or three substituents selected from the group consisting of halogen, cyano, hydroxy, and methoxy;
  • w 0, 1, 2 or 3;
  • x is 0 or 1
  • z 0, 1, 2 or 3;
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein A is
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein A is
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein x is 0.
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein x is 1.
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein L is
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein L is
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein
  • R 1 is —C(O)R 10a and R 2 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 2 is —C(O)R 10b and R 1 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein R 10a is C 1 -C 4 alkyl and R 10b is C 1 -C 4 alkyl.
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the C 6 aryl and the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two halogen or C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein at least one of R 1 and R 2 is C 1 -C 4 alkyl.
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein R 1 and R 2 each independently C 1 -C 4 alkyl.
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein at least one of R 1 and R 2 is hydrogen.
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein at least one of R 1 and R 2 is C 3 -C 6 cycloalkyl optionally substituted by one or two R 15 groups.
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein at least one of R 1 and R 2 is 5-6 membered heteroaryl optionally substituted by one or two R 15 groups.
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein L is
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein
  • R 1 is —C(O)R 10a and R 2 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 2 is —C(O)R 10b and R 1 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )]—(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 6 aryl), or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the C 6 aryl and the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two halogen or C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the aryl and the heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein each R 13 and R 14 is hydrogen and each z is 1.
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyridinyl and R 10b is —CH 2 -pyridinyl, wherein each pyridinyl is optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyridinyl optionally substituted by one or two C 1 -C 4 alkyl groups and R 10b is —CH 2 -pyrazolyl optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )]—(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the C 6 aryl and the 5-6 membered heteroaryl in R 10a are each independently optionally substituted by one or two halogen or C 1 -C 4 alkyl groups, and R 10b is C 1 -C 4 alkyl optionally substituted by C 1 -C 6 alkoxy.
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein each R 13 and R 14 is hydrogen and each z is 1.
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein R 10a is —(CH 2 )-(5-6 membered heteroaryl) optionally substituted by one or two C 1 -C 4 alkyl groups and R 10b is C 1 -C 4 alkyl optionally substituted by C 1 -C 2 alkoxy.
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyridinyl and R 10b is —CH 2 CH 2 —O—CH 3 .
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein R 1 is —C(O)R 10a and R 2 is C 3 -C 6 cycloalkyl optionally substituted by one or two R 15 groups.
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein each R 13 and R 14 is hydrogen and each z is 1.
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -(5-6 membered heteroaryl) optionally substituted by one or two halogen or C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyridinyl optionally substituted by one or two C 1 -C 4 alkyl groups and R 2 is cyclopropyl.
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein L is
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein
  • R 1 is —C(O)R 10a and R 2 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 2 is —C(O)R 10b and R 1 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )]—(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z -(6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the C 6 aryl and the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two halogen or C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) optionally substituted by one or two C 1 -C 4 alkyl groups and R 10b is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyrazolyl optionally substituted by one or two C 1 -C 4 alkyl groups and R 10b is —CH 2 -pyrazolyl optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein L is
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein
  • R 1 is —C(O)R 10a and R 2 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 2 is —C(O)R 10b and R 1 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )]—(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the C 6 aryl and the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two halogen or C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein each R 13 and R 14 is hydrogen and each z is 1.
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyridinyl optionally substituted by one or two C 1 -C 4 alkyl groups and R 10b is —CH 2 -pyridinyl optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein L is
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein
  • R 1 is —C(O)R 10a and R 2 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 2 is —C(O)R 10b and R 1 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 6 aryl), or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the C 6 aryl and the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two halogen or C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein each R 13 and R 14 is hydrogen and each z is 1.
  • Embodiments described herein relate to a compound of formula (IV), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyridinyl optionally substituted by one or two C 1 -C 4 alkyl groups and R 10b is —CH 2 -pyridinyl optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IVa)
  • L is —(C 4 -C 10 cycloalkyl)- optionally substituted by one to three substituents selected from the group consisting of halogen, cyano, C 1 -C 4 alkyl, hydroxy, and C 1 -C 4 alkoxy;
  • R 1 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10a , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups;
  • R 2 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups;
  • R 3 and R 4 are each independently hydrogen, halogen, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, or C 3 -C 6 cycloalkyl;
  • R 7 and R 8 are each independently hydrogen, halogen, cyano, C 1 -C 2 alkyl, hydroxy, C 1 -C 2 alkoxy, or —N(R 11 )(R 12 ), wherein the C 1 -C 2 alkyl and the C 1 -C 2 alkoxy are each independently optionally substituted by halogen or hydroxy;
  • R 10a and R 10b are each independently hydrogen, C 1 -C 4 alkyl, —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl), wherein the C 1 -C 4 alkyl, the C 4 -C 10 cycloalkyl, the 4-6 membered heterocycloalkyl, the C 6 -C 10 aryl, and the 5-10 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one, two or three halogen, cyano, C 1 -C 6 alkyl, hydroxy, C 1 -C
  • each R 11 , R 12 , R 13 , R 14 and R 15 is independently hydrogen, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, C 3 -C 6 cycloalkyl, or 3-6 membered heterocycloalkyl, wherein the C 1 -C 4 alkyl, the C 3 -C 6 cycloalkyl, and the 3-6 membered heterocycloalkyl are each independently optionally substituted by one, two or three substituents selected from the group consisting of halogen, cyano, hydroxy, and methoxy;
  • w 0, 1, 2 or 3;
  • x is 0 or 1
  • z 0, 1, 2 or 3;
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein x is 0.
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein x is 1.
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein L is
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein L is
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein
  • R 1 is —C(O)R 10a and R 2 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 2 is —C(O)R 10b and R 1 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein R 10a is C 1 -C 4 alkyl and R 10b is C 1 -C 4 alkyl.
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z (C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl),
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the C 6 aryl and the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two halogen or C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein at least one of R 1 and R 2 is C 1 -C 4 alkyl.
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein R 1 and R 2 each independently C 1 -C 4 alkyl.
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein at least one of R 1 and R 2 is hydrogen.
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein at least one of R 1 and R 2 is C 3 -C 6 cycloalkyl optionally substituted by one or two R 15 groups.
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein at least one of R 1 and R 2 is 5-6 membered heteroaryl optionally substituted by one or two R 15 groups.
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein L is
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein
  • R 1 is —C(O)R 10a and R 2 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 2 is —C(O)R 10b and R 1 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 ary
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 6 aryl), or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the C 6 aryl and the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two halogen or C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the aryl and the heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein each R 13 and R 14 is hydrogen and each z is 1.
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyridinyl and R 10b is —CH 2 -pyridinyl, wherein each pyridinyl is optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyridinyl optionally substituted by one or two C 1 -C 4 alkyl groups and R 10b is —CH 2 -pyrazolyl optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 ary
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the C 6 aryl and the 5-6 membered heteroaryl in R 10a are each independently optionally substituted by one or two halogen or C 1 -C 4 alkyl groups, and R 10b is C 1 -C 4 alkyl optionally substituted by C 1 -C 6 alkoxy.
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein each R 13 and R 14 is hydrogen and each z is 1.
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein R 10a is —(CH 2 )-(5-6 membered heteroaryl) optionally substituted by one or two C 1 -C 4 alkyl groups and R 10b is C 1 -C 4 alkyl optionally substituted by C 1 -C 2 alkoxy.
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyridinyl and R 10b is —CH 2 CH 2 —O—CH 3 .
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein R 1 is —C(O)R 10a and R 2 is C 3 -C 6 cycloalkyl optionally substituted by one or two R 15 groups.
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 ary
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein each R 13 and R 14 is hydrogen and each z is 1.
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -(5-6 membered heteroaryl) optionally substituted by one or two halogen or C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyridinyl optionally substituted by one or two C 1 -C 4 alkyl groups and R 2 is cyclopropyl.
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein L is
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein
  • R 1 is —C(O)R 10a and R 2 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 2 is —C(O)R 10b and R 1 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 ary
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )]—(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the C 6 aryl and the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two halogen or C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) optionally substituted by one or two C 1 -C 4 alkyl groups and R 10b is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyrazolyl optionally substituted by one or two C 1 -C 4 alkyl groups and R 10b is —CH 2 -pyrazolyl optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein L is
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein
  • R 1 is —C(O)R 10a and R 2 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 2 is —C(O)R 10b and R 1 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 ary
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the C 6 aryl and the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two halogen or C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein each R 13 and R 14 is hydrogen and each z is 1.
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyridinyl optionally substituted by one or two C 1 -C 4 alkyl groups and R 10b is —CH 2 -pyridinyl optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein L is
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein
  • R 1 is —C(O)R 10a and R 2 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 2 is —C(O)R 10b and R 1 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 ary
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 6 aryl), or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the C 6 aryl and the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two halogen or C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein each R 13 and R 14 is hydrogen and each z is 1.
  • Embodiments described herein relate to a compound of formula (IVa), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyridinyl optionally substituted by one or two C 1 -C 4 alkyl groups and R 10b is —CH 2 -pyridinyl optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IVb)
  • L is —(C 4 -C 10 cycloalkyl)- optionally substituted by one to three substituents selected from the group consisting of halogen, cyano, C 1 -C 4 alkyl, hydroxy, and C 1 -C 4 alkoxy;
  • R 1 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10a , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups;
  • R 2 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups;
  • R 3 and R 4 are each independently hydrogen, halogen, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, or C 3 -C 6 cycloalkyl;
  • R 10a and R 10b are each independently hydrogen, C 1 -C 4 alkyl, —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl), wherein the C 1 -C 4 alkyl, the C 4 -C 10 cycloalkyl, the 4-6 membered heterocycloalkyl, the C 6 -C 10 aryl, and the 5-10 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one, two or three halogen, cyano, C 1 -C 6 alkyl, hydroxy, C 1 -C
  • each R 11 , R 12 , R 13 , R 14 and R 15 is independently hydrogen, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, C 3 -C 6 cycloalkyl, or 3-6 membered heterocycloalkyl, wherein the C 1 -C 4 alkyl, the C 3 -C 6 cycloalkyl, and the 3-6 membered heterocycloalkyl are each independently optionally substituted by one, two or three substituents selected from the group consisting of halogen, cyano, hydroxy, and methoxy;
  • w 0, 1, 2 or 3;
  • x is 0 or 1
  • z 0, 1, 2 or 3;
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein x is 0.
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein x is 1.
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein L is
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein L is
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein
  • R 1 is —C(O)R 10a and R 2 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 2 is —C(O)R 10b and R 1 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein R 10a is C 1 -C 4 alkyl and R 10b is C 1 -C 4 alkyl.
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 ary
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )]—(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z -(6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the C 6 aryl and the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two halogen or C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein at least one of R 1 and R 2 is C 1 -C 4 alkyl.
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein R 1 and R 2 each independently C 1 -C 4 alkyl.
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein at least one of R 1 and R 2 is hydrogen.
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein at least one of R 1 and R 2 is C 3 -C 6 cycloalkyl optionally substituted by one or two R 15 groups.
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein at least one of R 1 and R 2 is 5-6 membered heteroaryl optionally substituted by one or two R 15 groups.
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein L is
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein
  • R 1 is —C(O)R 10a and R 2 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 2 is —C(O)R 10b and R 1 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 ary
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 6 aryl), or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the C 6 aryl and the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two halogen or C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the aryl and the heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein each R 13 and R 14 is hydrogen and each z is 1.
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyridinyl and R 10b is —CH 2 -pyridinyl, wherein each pyridinyl is optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyridinyl optionally substituted by one or two C 1 -C 4 alkyl groups and R 10b is —CH 2 -pyrazolyl optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 ary
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the C 6 aryl and the 5-6 membered heteroaryl in R 10a are each independently optionally substituted by one or two halogen or C 1 -C 4 alkyl groups, and R 10b is C 1 -C 4 alkyl optionally substituted by C 1 -C 6 alkoxy.
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein each R 13 and R 14 is hydrogen and each z is 1.
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein R 10a is —(CH 2 )-(5-6 membered heteroaryl) optionally substituted by one or two C 1 -C 4 alkyl groups and R 10b is C 1 -C 4 alkyl optionally substituted by C 1 -C 2 alkoxy.
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyridinyl and R 10b is —CH 2 CH 2 —O—CH 3 .
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein R 1 is —C(O)R 10a and R 2 is C 3 -C 6 cycloalkyl optionally substituted by one or two R 15 groups.
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 ary
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein each R 13 and R 14 is hydrogen and each z is 1.
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -(5-6 membered heteroaryl) optionally substituted by one or two halogen or C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyridinyl optionally substituted by one or two C 1 -C 4 alkyl groups and R 2 is cyclopropyl.
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein L is
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein
  • R 1 is —C(O)R 10a and R 2 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 2 is —C(O)R 10b and R 1 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 ary
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z -(6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the C 6 aryl and the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two halogen or C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) optionally substituted by one or two C 1 -C 4 alkyl groups and R 10b is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyrazolyl optionally substituted by one or two C 1 -C 4 alkyl groups and R 10b is —CH 2 -pyrazolyl optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein L is
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein
  • R 1 is —C(O)R 10a and R 2 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 2 is —C(O)R 10b and R 1 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 ary
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the C 6 aryl and the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two halogen or C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein each R 13 and R 14 is hydrogen and each z is 1.
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyridinyl optionally substituted by one or two C 1 -C 4 alkyl groups and R 10b is —CH 2 -pyridinyl optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein L is
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein
  • R 1 is —C(O)R 10a and R 2 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 2 is —C(O)R 10b and R 1 is hydrogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C(O)R 10b , or 5-6 membered heteroaryl, wherein the C 3 -C 6 cycloalkyl and the 5-6 membered heteroaryl are independently optionally substituted by one or two R 15 groups; or
  • R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein R 1 is —C(O)R 10a and R 2 is —C(O)R 10b .
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z (C 6 -C 10 aryl), or —[C(R 13 )(R 14 )] z -(5-10 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 4 -C 10 cycloalkyl), —[C(R 13 )(R 14 )] z -(4-6 membered heterocycloalkyl), —[C(R 13 )(R 14 )] z —(C 6 -C 10 aryl),
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z —(C 6 aryl) or —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z —(C 6 aryl), or -[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the C 6 aryl and the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two halogen or C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein R 10a is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl) and R 10b is —[C(R 13 )(R 14 )] z -(5-6 membered heteroaryl), wherein the 5-6 membered heteroaryl in R 10a and R 10b are each independently optionally substituted by one or two C 1 -C 4 alkyl groups.
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein each R 13 and R 14 is hydrogen and each z is 1.
  • Embodiments described herein relate to a compound of formula (IVb), or a pharmaceutically acceptable salt thereof, wherein R 10a is —CH 2 -pyridinyl optionally substituted by one or two C 1 -C 4 alkyl groups and R 10b is —CH 2 -pyridinyl optionally substituted by one or two C 1 -C 4 alkyl groups.
  • the compound is selected from:
  • Embodiments relate to a pharmaceutical composition
  • a pharmaceutical composition comprising a compound of any of the embodiments of the compounds of formula (I), formula (II), formula (III), formula (IV), formula (IVa), or formula (IVb), or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier or diluent.
  • Embodiments relate to a pharmaceutical composition
  • a pharmaceutical composition comprising a compound of any of the embodiments of the compounds of formula (I), formula (II), formula (III), formula (IV), formula (IVa), or formula (IVb), or a pharmaceutically acceptable salt thereof, with an anti-tumor agent or with radiation therapy, for the treatment of cancer.
  • Embodiments relate to a pharmaceutical composition
  • a pharmaceutical composition comprising a compound of any of the embodiments of the compounds of formula (I), formula (II), formula (III), formula (IV), formula (IVa), or formula (IVb), or a pharmaceutically acceptable salt thereof, with an anti-tumor agent, for the treatment of cancer.
  • Embodiments relate to a method of treating abnormal cell growth in a mammal comprising administering to the mammal an amount of a composition of any of the embodiments of the compounds of formula (I), formula (II), formula (III), formula (IV), formula (IVa), or formula (IVb), or a pharmaceutically acceptable salt thereof, that is effective in treating abnormal cell growth.
  • Embodiments relate to a method of treating abnormal cell growth in a mammal comprising administering to the mammal an amount of a compound of any of the embodiments of the compounds of formula (I), formula (II), formula (III), formula (IV), formula (IVa), or formula (IVb), or a pharmaceutically acceptable salt thereof, that is effective in treating abnormal cell growth.
  • Embodiments relate to the method of treating abnormal cell growth, wherein the abnormal cell growth is cancer.
  • Embodiments relate to the method of treating cancer, wherein the cancer is selected from the group consisting of basal cell cancer, medulloblastoma cancer, liver cancer, rhabdomyosarcoma, lung cancer, bone cancer, pancreatic cancer, skin cancer, cancer of the head or neck, cutaneous or intraocular melanoma, uterine cancer, ovarian cancer, rectal cancer, cancer of the anal region, stomach cancer, colon cancer, breast cancer, uterine cancer, carcinoma of the fallopian tubes, carcinoma of the endometrium, carcinoma of the cervix, carcinoma of the vagina, carcinoma of the vulva, Hodgkin's disease, cancer of the esophagus, cancer of the small intestine, cancer of the endocrine system, cancer of the thyroid gland, cancer of the parathyroid gland, cancer of the adrenal gland, sarcoma of soft tissue, cancer of the urethra, cancer of the penis, prostate cancer, chronic or acute leukemia, lymphocytic lympho
  • Embodiments relate to the method of treating lung cancer, wherein the cancer is selected from the group consisting of lung cancer, cancer of the head or neck, colon cancer, breast cancer, and ovarian cancer, or a combination of one or more of the foregoing cancers.
  • halogen refers to a fluorine, chlorine, bromine, or iodine atom or fluoro, chloro, bromo, or iodo. Additionally, the term “halogen” refers to F, Cl, Br, or I. The terms fluorine, fluoro and F, for example, are understood to be equivalent herein.
  • alkyl refers to saturated monovalent hydrocarbon radicals containing, in certain embodiments, from one to six, from one to four or from one to three carbon atoms, having straight or branched moieties.
  • C 1 -C 6 alkyl refers to an alkyl radical containing from one to six carbon atoms, having straight or branched moieties.
  • C 1 -C 6 alkyl includes within its definition the terms “C 1 -C 2 alkyl”, “C 1 -C 3 alkyl”, and “C 1 -C 4 alkyl”.
  • alkyl groups include, but are not limited to, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, 2-pentyl, 3-pentyl, isopentyl, neopentyl, (R)-2-methylbutyl, (S)-2-methylbutyl, 3-methylbutyl, 2,3-dimethylpropyl, 2,3-dimethylbutyl, hexyl, and the like.
  • alkoxy refers to an alkyl radical that is single bonded to an oxygen atom. The attachment point of an alkoxy radical to a molecule is through the oxygen atom. An alkoxy radical may be depicted as alkyl-O—.
  • C 1 -C 6 alkoxy refers to an alkoxy radical containing from one to six carbon atoms, having straight or branched moieties.
  • C 1 -C 2 alkoxy and “C 1 -C 4 alkoxy” refer to an alkoxy radical containing from one to two carbon atoms and from one to four carbon atoms, respectively, having straight or branched moieties.
  • Alkoxy groups include, but are not limited to, methoxy, ethoxy, propoxy, isopropoxy, butoxy, hexyloxy, and the like.
  • cycloalkyl refers to a monocyclic, fused or bridged bicyclic or tricyclic carbocyclic ring group containing, in certain embodiments, from three to ten carbon atoms. As used herein, a cycloalkyl group rings may optionally contain one or two double bonds. The term “cycloalkyl” also includes spirocyclic cycloalkyl groups, including multi-ring systems joined by a single atom.
  • C 3 -C 10 cycloalkyl contains from three to ten, from three to seven, from three to four, from three to six, from four to ten, and from five to seven carbon atoms, respectively.
  • Cycloalkyl groups include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclopentenyl, cyclohexenyl, bicyclo[2.2.1]heptanyl, bicyclo[3.2.1]octanyl, bicyclo[5.2.0]nonanyl, adamantanyl, spiro[3.3]heptanyl, and the like.
  • heterocycloalkyl refers to a non-aromatic, monocyclic, fused or bridged bicyclic or tricyclic or spirocyclic ring group containing, in certain embodiments, a total of three to ten ring atoms, in which one to four ring atoms are heteroatoms independently selected from nitrogen, oxygen, and sulfur, and wherein the sulfur atom may be optionally oxidized with one or two oxygen atoms, the remaining ring atoms being carbon, with the proviso that such ring systems may not contain two adjacent oxygen atoms or two adjacent sulfur atoms.
  • the heterocycloalkyl ring may also be substituted by an oxo ( ⁇ O) group at any available carbon atom.
  • the rings may also have one or more double bonds. Furthermore, such groups may be bonded to the remainder of the compounds of embodiments disclosed herein through either a carbon atom or a heteroatom, if possible.
  • the terms “3-10 membered heterocycloalkyl”, “4-10 membered heterocycloalkyl”, “3-7 membered heterocycloalkyl”, “3-6 membered heterocycloalkyl”, and “4-6 membered heterocycloalkyl” contain from three to ten, from four to ten, from three to seven, from three to six carbon atoms, and from four to six carbon atoms, respectively. Examples of saturated heterocycloalkyl groups include, but are not limited to:
  • Suitable partially unsaturated heterocycloalkyl groups include, but are not limited to:
  • aryl refers to a group derived from an aromatic hydrocarbon containing in certain embodiments, from six to ten carbon atoms.
  • C 6 -C 10 aryl contains from five to ten carbon atoms. Examples of such groups include, but are not limited to, phenyl and naphthyl.
  • aryl also includes fused polycyclic aromatic ring systems in which an aromatic ring is fused to one or more rings. Examples include, but are not limited to, 1-naphthyl, 2-naphthyl, 1-anthracyl and 2-anthracyl.
  • aryl is a group in which an aromatic ring is fused to one or more non-aromatic rings, such as in an indanyl, phenanthridinyl, or tetrahydronaphthyl, where the radical or point of attachment is on the aromatic ring.
  • heteroaryl refers to an aromatic monocyclic or bicyclic heterocyclic group having a total of from 5 to 12 atoms in its ring, and containing from 2 to 9 carbon atoms and from one to four heteroatoms each independently selected from nitrogen, oxygen, and sulfur, with the proviso that the ring of said group does not contain two adjacent oxygen atoms or two adjacent sulfur atoms.
  • heteroaryl contains five, six, from five to ten, from five to twelve, contain from five to six, from four to six ring atoms, and from three to five ring atoms, respectively.
  • the heteroaryl groups include benzo-fused ring systems.
  • heteroaryl groups include, but are not limited to, pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, isoxazolyl, isothiazolyl, triazolyl, oxadiazolyl, furazanyl, thiadiazolyl, thiazolyl, tetrazolyl, pyridinyl, pyrazinyl, pyrimidinyl, pyridazinyl, triazinyl, indolyl, isoindolyl, indolizinyl, benzofuranyl, benzothiophenyl, indazolyl, benzimidazolyl, benzoxazolyl, furo[3,2-b]pyridinyl, benzothiazolyl, benzofurazanyl, purinyl, quinolinyl, isoquinolinyl, quinazolinyl, quinoxalinyl,
  • benzo-fused unsaturated nitrogen heterocycles which refer to a heterocyclic group in which a heteroatomic ring is fused to one or more aromatic rings.
  • examples include, but are not limited to, indolinyl, isoindolinyl, tetrahydroquinolinyl, tetrahydroisoquinolinyl, and the like.
  • treating means reversing, alleviating, inhibiting the progress of, or preventing the disorder or condition to which such term applies, or one or more symptoms of such disorder or condition.
  • treatment refers to the act of treating as “treating” is defined immediately above.
  • an “effective” amount refers to an amount of a substance, agent, compound, or composition that is of sufficient quantity to result in a decrease in severity of disease symptoms, an increase in frequency and duration of disease symptom-free periods, or a prevention of impairment or disability due to the disease affliction—either as a single dose or according to a multiple dose regimen, alone or in combination with other agents or substances.
  • One of ordinary skill in the art would be able to determine such amounts based on such factors as the subject's size, the severity of the subject's symptoms, and the particular composition or route of administration selected.
  • the subject may be a human or non-human mammal (e.g., rabbit, rat, mouse, monkey or other lower-order primate).
  • Embodiments disclosed herein include isotopically-labeled compounds, which are identical to those recited in formula (I), formula (II), formula (III), formula (IV), formula (IVa), or formula (IVb), but for the fact that one or more atoms are replaced by an atom having an atomic mass or mass number different from the atomic mass or mass number usually found in nature.
  • isotopes that can be incorporated into compounds of the embodiments disclosed herein include isotopes of hydrogen, carbon, nitrogen, oxygen, phosphorous, sulfur, fluorine and chlorine, such as, but not limited to, 2 H, 3 H, 13 C, 14 C, 15 N, 18 O, 17 O, 31 P, 32 P 35 S, 18 F, and 36 Cl, respectively.
  • Isotopically-labeled compounds of embodiments disclosed herein can generally be prepared by carrying out the procedures disclosed in the Schemes and/or in the Examples and Preparations below, by substituting a readily available isotopically-labeled reagent for a non-isotopically-labeled reagent.
  • compositions described herein relate to the pharmaceutically acceptable salts of the compounds described herein.
  • Pharmaceutically acceptable salts of the compounds described herein include the acid addition and base addition salts thereof.
  • Suitable acid addition salts are formed from acids which form non-toxic salts.
  • suitable acid addition salts i.e., salts containing pharmacologically acceptable anions, include, but are not limited to, the acetate, acid citrate, adipate, aspartate, benzoate, besylate, bicarbonate/carbonate, bisulphate/sulphate, bitartrate, borate, camsylate, citrate, cyclamate, edisylate, esylate, ethanesulfonate, formate, fumarate, gluceptate, gluconate, glucuronate, hexafluorophosphate, hibenzate, hydrochloride/chloride, hydrobromide/bromide, hydroiodide/iodide, isethionate, lactate, malate, maleate, malonate, mesylate, methane
  • Suitable base addition salts are formed from bases which form non-toxic salts.
  • suitable base salts include the aluminium, arginine, benzathine, calcium, choline, diethylamine, diolamine, glycine, lysine, magnesium, meglumine, olamine, potassium, sodium, tromethamine and zinc salts.
  • the compounds described herein that are basic in nature are capable of forming a wide variety of salts with various inorganic and organic acids.
  • the acids that may be used to prepare pharmaceutically acceptable acid addition salts of such basic compounds described herein are those that form non-toxic acid addition salts, e.g., salts containing pharmacologically acceptable anions, such as the hydrochloride, hydrobromide, hydroiodide, nitrate, sulfate, bisulfate, phosphate, acid phosphate, isonicotinate, acetate, lactate, salicylate, citrate, acid citrate, tartrate, pantothenate, bitartrate, ascorbate, succinate, maleate, gentisinate, fumarate, gluconate, glucuronate, saccharate, formate, benzoate, glutamate, methanesulfonate, ethanesulfonate, benzenesulfonate, p-toluenesulfon
  • the chemical bases that may be used as reagents to prepare pharmaceutically acceptable base salts of those compounds of the compounds described herein that are acidic in nature are those that form non-toxic base salts with such compounds.
  • Such non-toxic base salts include, but are not limited to those derived from such pharmacologically acceptable cations such as alkali metal cations (e.g., potassium and sodium) and alkaline earth metal cations (e.g., calcium and magnesium), ammonium or water-soluble amine addition salts such as N-methylglucamine-(meglumine), and the lower alkanolammonium and other base salts of pharmaceutically acceptable organic amines.
  • the compounds of the embodiments described herein include all stereoisomers (e.g., cis and trans isomers) and all optical isomers of compounds described herein (e.g., R and S enantiomers), as well as racemic, diastereomeric and other mixtures of such isomers. While all stereoisomers are encompassed within the scope of our claims, one skilled in the art will recognize that particular stereoisomers may be preferred.
  • the compounds described herein can exist in several tautomeric forms, including the enol and imine form, and the keto and enamine form and geometric isomers and mixtures thereof. All such tautomeric forms are included within the scope of the present embodiments. Tautomers exist as mixtures of a tautomeric set in solution. In solid form, usually one tautomer predominates. Even though one tautomer may be described, the present embodiments includes all tautomers of the present compounds.
  • the present embodiments also include atropisomers of the compounds described herein.
  • Atropisomers refer to compounds that can be separated into rotationally restricted isomers.
  • Hemisalts of acids and bases may also be formed, for example, hemisulphate and hemicalcium salts.
  • solvate is used herein to describe a molecular complex comprising a compound described herein and one or more pharmaceutically acceptable solvent molecules, for example, ethanol.
  • the compounds described herein may also exist in unsolvated and solvated forms. Accordingly, some embodiments relate to the hydrates and solvates of the compounds described herein.
  • tautomeric isomerism (‘tautomerism’) can occur. This can take the form of proton tautomerism in compounds described herein containing, for example, an imino, keto, or oxime group, or so-called valence tautomerism in compounds which contain an aromatic moiety. A single compound may exhibit more than one type of isomerism.
  • Cis/trans isomers may be separated by conventional techniques well known to those skilled in the art, for example, chromatography and fractional crystallisation.
  • the racemate (or a racemic precursor) may be reacted with a suitable optically active compound, for example, an alcohol, or, in the case where a compound described herein contains an acidic or basic moiety, a base or acid such as 1-phenylethylamine or tartaric acid.
  • a suitable optically active compound for example, an alcohol, or, in the case where a compound described herein contains an acidic or basic moiety, a base or acid such as 1-phenylethylamine or tartaric acid.
  • the resulting diastereomeric mixture may be separated by chromatography and/or fractional crystallization and one or both of the diastereoisomers converted to the corresponding pure enantiomer(s) by means well known to a skilled person.
  • Further embodiments relate to methods of treating abnormal cell growth in a mammal. Additional embodiments relate to a method of treating abnormal cell growth in a mammal comprising administering to the mammal an amount of a compound described herein that is effective in treating abnormal cell growth.
  • the abnormal cell growth is cancer.
  • the cancer is selected from the group consisting of lung cancer, mesothelioma, bone cancer, pancreatic cancer, skin cancer, cancer of the head or neck, cutaneous or intraocular melanoma, uterine cancer, ovarian cancer, rectal cancer, cancer of the anal region, stomach cancer, hepatic carcinoma, colon cancer, breast cancer, uterine cancer, carcinoma of the fallopian tubes, carcinoma of the endometrium, carcinoma of the cervix, carcinoma of the vagina, carcinoma of the vulva, Hodgkin's disease, cancer of the esophagus, cancer of the small intestine, cancer of the endocrine system, cancer of the thyroid gland, cancer of the parathyroid gland, cancer of the adrenal gland, sarcoma of soft tissue, cancer of the urethra, cancer of the penis, prostate cancer, hematology malignancy, chronic or acute leukemia, lymphocytic lymphomas, cancer of the bladder, cancer of the kidney or ureter,
  • Additional embodiments relate to methods of treating cancer solid tumors in a mammal. Some embodiments relate to the treatment of cancer solid tumor in a mammal comprising administering to the mammal an amount of a compound described herein that is effective in treating said cancer solid tumor.
  • the cancer solid tumor is breast, lung, colon, brain, prostate, stomach, pancreatic, ovarian, skin (melanoma), endocrine, uterine, testicular, or bladder.
  • compositions for treating abnormal cell growth in a mammal comprising an amount of a compound described herein that is effective in treating abnormal cell growth, and a pharmaceutically acceptable carrier.
  • Additional embodiments relate to a method of treating abnormal cell growth in a mammal, including a human, comprising administering to the mammal an amount of a compound described herein, or a pharmaceutically acceptable salt, solvate, hydrate or prodrug thereof, that is effective in treating abnormal cell growth.
  • the abnormal cell growth is cancer, including, but not limited to, lung cancer, bone cancer, pancreatic cancer, skin cancer, cancer of the head or neck, cutaneous or intraocular melanoma, uterine cancer, ovarian cancer, rectal cancer, cancer of the anal region, stomach cancer, colon cancer, breast cancer, uterine cancer, carcinoma of the fallopian tubes, carcinoma of the endometrium, carcinoma of the cervix, carcinoma of the vagina, carcinoma of the vulva, Hodgkin's Disease, cancer of the esophagus, cancer of the small intestine, cancer of the endocrine system, cancer of the thyroid gland, cancer of the parathyroid gland, cancer of the adrenal gland, sarcoma of soft tissue, cancer of the urethra, cancer of the penis, prostate cancer, chronic or acute leukemia, lymphocytic lymphomas, cancer of the bladder, cancer of the kidney or ureter, renal cell carcinoma, carcinoma of the renal pelvis, neoplasms
  • the method comprises comprising administering to a mammal an amount of a compound described herein that is effective in treating said cancer solid tumor.
  • the solid tumor is breast, lung, colon, brain, prostate, stomach, pancreatic, ovarian, skin (melanoma), endocrine, uterine, testicular, and bladder cancer.
  • said abnormal cell growth is a benign proliferative disease, including, but not limited to, psoriasis, benign prostatic hypertrophy or restinosis.
  • Some embodiments relate to a method of treating abnormal cell growth in a mammal which comprises administering to said mammal an amount of a compound described herein, or a pharmaceutically acceptable salt, solvate, hydrate or prodrug thereof, that is effective in treating abnormal cell growth in combination with an anti-tumor agent selected from the group consisting of mitotic inhibitors, alkylating agents, anti-metabolites, intercalating antibiotics, growth factor inhibitors, cell cycle inhibitors, enzymes, topoisomerase inhibitors, biological response modifiers, antibodies, cytotoxics, anti-hormones, and anti-androgens.
  • an anti-tumor agent selected from the group consisting of mitotic inhibitors, alkylating agents, anti-metabolites, intercalating antibiotics, growth factor inhibitors, cell cycle inhibitors, enzymes, topoisomerase inhibitors, biological response modifiers, antibodies, cytotoxics, anti-hormones, and anti-androgens.
  • Additional embodiments relate to a pharmaceutical composition for treating abnormal cell growth in a mammal, including a human, comprising an amount of a compound described herein, or a pharmaceutically acceptable salt, solvate, hydrate or prodrug thereof, that is effective in treating abnormal cell growth, and a pharmaceutically acceptable carrier.
  • said abnormal cell growth is cancer, including, but not limited to, lung cancer, bone cancer, pancreatic cancer, skin cancer, cancer of the head or neck, cutaneous or intraocular melanoma, uterine cancer, ovarian cancer, rectal cancer, cancer of the anal region, stomach cancer, colon cancer, breast cancer, uterine cancer, carcinoma of the fallopian tubes, carcinoma of the endometrium, carcinoma of the cervix, carcinoma of the vagina, carcinoma of the vulva, Hodgkin's Disease, cancer of the esophagus, cancer of the small intestine, cancer of the endocrine system, cancer of the thyroid gland, cancer of the parathyroid gland, cancer of the adrenal gland, sarcoma of soft tissue, cancer of the urethra, cancer of the penis, prostate cancer, chronic or acute leukemia, lymphocytic lymphomas, cancer of the bladder, cancer of the kidney or ureter, renal cell carcinoma, carcinoma of the renal pelvis, neoplasms
  • compositions for treating abnormal cell growth contemplate a pharmaceutical composition for treating abnormal cell growth wherein the composition includes a compound described herein, or a pharmaceutically acceptable salt, solvate, or hydrate thereof, that is effective in treating abnormal cell growth, and another anti-tumor agent selected from the group consisting of mitotic inhibitors, alkylating agents, anti-metabolites, intercalating antibiotics, growth factor inhibitors, cell cycle inhibitors, enzymes, topoisomerase inhibitors, biological response modifiers, antibodies, cytotoxics, anti-hormones, and anti-androgens.
  • another anti-tumor agent selected from the group consisting of mitotic inhibitors, alkylating agents, anti-metabolites, intercalating antibiotics, growth factor inhibitors, cell cycle inhibitors, enzymes, topoisomerase inhibitors, biological response modifiers, antibodies, cytotoxics, anti-hormones, and anti-androgens.
  • Yet more embodiments relate to a method of treating a disorder associated with angiogenesis in a mammal, including a human, comprising administering to said mammal an amount of a compound described herein, as defined above, or a pharmaceutically acceptable salt, solvate, hydrate or prodrug thereof, that is effective in treating said disorder in combination with one or more anti-tumor agents listed above.
  • Such disorders include cancerous tumors such as melanoma; ocular disorders such as age-related macular degeneration, presumed ocular histoplasmosis syndrome, and retinal neovascularization from proliferative diabetic retinopathy; rheumatoid arthritis; bone loss disorders such as osteoporosis, Paget's disease, humoral hypercalcemia of malignancy, hypercalcemia from tumors metastatic to bone, and osteoporosis induced by glucocorticoid treatment; coronary restenosis; and certain microbial infections including those associated with microbial pathogens selected from adenovirus, hantaviruses, Borrelia burgdorferi, Yersinia spp., Bordetella pertussis , and group A Streptococcus.
  • Some embodiments relate to a method of (and to a pharmaceutical composition for) treating abnormal cell growth in a mammal which comprise an amount of a compound described herein, or a pharmaceutically acceptable salt, solvate, or hydrate thereof, in combination with an amount of one or more substances selected from anti-angiogenesis agents, signal transduction inhibitors inhibitor (e.g., inhibiting the means by which regulatory molecules that govern the fundamental processes of cell growth, differentiation, and survival communicated within the cell), and antiproliferative agents, which amounts are together effective in treating said abnormal cell growth.
  • signal transduction inhibitors inhibitor e.g., inhibiting the means by which regulatory molecules that govern the fundamental processes of cell growth, differentiation, and survival communicated within the cell
  • antiproliferative agents which amounts are together effective in treating said abnormal cell growth.
  • Anti-angiogenesis agents such as MMP-2 (matrix-metalloprotienase 2) inhibitors, MMP-9 (matrix-metalloprotienase 9) inhibitors, and COX-II (cyclooxygenase II) inhibitors, can be used in conjunction with a compound described herein in the methods and pharmaceutical compositions described herein.
  • MMP-2 matrix-metalloprotienase 2
  • MMP-9 matrix-metalloprotienase 9 inhibitors
  • COX-II cyclooxygenase II
  • Examples of useful COX-II inhibitors include CELEBREXTM (celecoxib), Bextra (valdecoxib), paracoxib, Vioxx (rofecoxib), and Arcoxia (etoricoxib).
  • Examples of useful matrix metalloproteinase inhibitors are described in WO 96/33172 (published Oct. 24, 1996), WO 96/27583 (published Mar.
  • MMP-2 and MMP-9 inhibitors are those that have little or no activity inhibiting MMP-1. More preferred, are those that selectively inhibit MMP-2 and/or MMP-9 relative to the other matrix-metalloproteinases (i.e. MMP-1, MMP-3, MMP-4, MMP-5, MMP-6, MMP-7, MMP-8, MMP-10, MMP-11, MMP-12, and MMP-13).
  • MMP-1, MMP-3, MMP-4, MMP-5, MMP-6, MMP-7, MMP-8, MMP-10, MMP-11, MMP-12, and MMP-13 matrix-metalloproteinases
  • MMP inhibitors useful in combination with the compounds described herein are AG-3340, RO 32-3555, RS 13-0830, and the following compounds:
  • VEGF inhibitors for example, sutent and axitinib
  • VEGF inhibitors are described in, for example in WO 99/24440 (published May 20, 1999), PCT International Application PCT/IB99/00797 (filed May 3, 1999), in WO 95/21613 (published Aug. 17, 1995), WO 99/61422 (published Dec. 2, 1999), U.S. Pat. No. 5,834,504 (issued Nov. 10, 1998), WO 98/50356 (published Nov. 12, 1998), U.S. Pat. No. 5,883,113 (issued Mar. 16, 1999), U.S. Pat. No. 5,886,020 (issued Mar. 23, 1999), U.S. Pat. No.
  • Avastin an anti-VEGF monoclonal antibody of Genentech, Inc. of South San Francisco, Calif.
  • angiozyme a synthetic ribozyme from Ribozyme (Boulder, Colo.) and Chiron (Emeryville, Calif.).
  • ErbB2 receptor inhibitors such as GW-282974 (Glaxo Wellcome plc), and the monoclonal antibodies AR-209 (Aronex Pharmaceuticals Inc. of The Woodlands, Tex., USA) and 2B-1 (Chiron), may be administered in combination with a compound described herein.
  • erbB2 inhibitors include Herceptin, 2C4, and pertuzumab.
  • Such erbB2 inhibitors include those described in WO 98/02434 (published Jan. 22, 1998), WO 99/35146 (published Jul. 15, 1999), WO 99/35132 (published Jul. 15, 1999), WO 98/02437 (published Jan. 22, 1998), WO 97/13760 (published Apr.
  • ErbB2 receptor inhibitors useful in the embodiments described herein are also described in U.S. Provisional Application No. 60/117,341, filed Jan. 27, 1999, and in U.S. Provisional Application No. 60/117,346, filed Jan. 27, 1999, both of which are herein incorporated by reference in their entirety.
  • Other erbb2 receptor inhibitors include TAK-165 (Takeda) and GW-572016 (Glaxo-Wellcome).
  • World Patent Application WO 92/20642 (published Nov. 26, 1992), refers to certain bis-mono and bicyclic aryl and heteroaryl compounds as tyrosine kinase inhibitors that are useful in inhibiting abnormal cell proliferation.
  • World Patent Applications WO96/16960 (published Jun. 6, 1996), WO 96/09294 (published Mar. 6, 1996), WO 97/30034 (published Aug. 21, 1997), WO 98/02434 (published Jan. 22, 1998), WO 98/02437 (published Jan.
  • Epidermal growth factor receptor (EGFR) inhibitors may be administered in combination with a compound of the presentation invention.
  • EGFR inhibitors include gefinitib, erlotinib, icotinib, afatinib and dacomitinib.
  • Monoclonal antibody inhibitors of EGFR, such as cetuximab, may also be combined with a compound of the present invention.
  • PI3K inhibitors such as PI3K beta inhibitors, may be administered in combination with a compound of the presentation invention.
  • Mammalian target of rapamycin (mTOR) inhibitors may be administered in combination with a compound of the presentation invention.
  • mTOR inhibitors include rapamycin analogs and ATP competitive inhibitors.
  • c-Met inhibitors may be administered in combination with a compound of the presentation invention.
  • Such c-Met inhibitors include crizotinib and ARQ-197.
  • Monoclonal antibody inhibitors of c-Met, such as METMab, may also be combined with a compound of the present invention.
  • CDK inhibitors may be administered in combination with a compound of the presentation invention.
  • Such CDK inhibitors include palbociclib.
  • MEK inhibitors may be administered in combination with a compound of the presentation invention.
  • Such MEK inhibitors include PD-325901.
  • PARP inhibitors may be administered in combination with a compound of the presentation invention.
  • JAK inhibitors may be administered in combination with a compound of the presentation invention.
  • An antagonist of a Programmed Death 1 protein may be administered in combination with a compound of the presentation invention.
  • antiproliferative agents that may be used with the compounds described herein include inhibitors of the enzyme farnesyl protein transferase and inhibitors of the receptor tyrosine kinase PDGFr, including the compounds disclosed and claimed in the following U.S. patent application Ser. No. 09/221,946 (filed Dec. 28, 1998); Ser. No. 09/454,058 (filed Dec. 2, 1999); Ser. No. 09/501,163 (filed Feb. 9, 2000); Ser. No. 09/539,930 (filed Mar. 31, 2000); Ser. No. 09/202,796 (filed May 22, 1997); Ser. No. 09/384,339 (filed Aug. 26, 1999); and Ser. No. 09/383,755 (filed Aug.
  • a compound described herein may also be used with other agents useful in treating abnormal cell growth or cancer, including, but not limited to, agents capable of enhancing antitumor immune responses, such as CTLA4 (cytotoxic lymphocyte antigen 4) antibodies, and other agents capable of blocking CTLA4; and anti-proliferative agents such as other farnesyl protein transferase inhibitors, for example the farnesyl protein transferase inhibitors described in the references cited in the “Background” section, supra.
  • CTLA4 cytotoxic lymphocyte antigen 4
  • anti-proliferative agents such as other farnesyl protein transferase inhibitors, for example the farnesyl protein transferase inhibitors described in the references cited in the “Background” section, supra.
  • Specific CTLA4 antibodies that can be used in the present embodiments include those described in U.S. Provisional Application 60/113,647 (filed Dec. 23, 1998) which is herein incorporated by reference in its entirety.
  • a compound described herein may be applied as a sole therapy or may involve one or more other anti-tumor substances, for example those selected from, for example, mitotic inhibitors, for example vinblastine; alkylating agents, for example cis-platin, oxaliplatin, carboplatin and cyclophosphamide; anti-metabolites, for example 5-fluorouracil, capecitabine, cytosine arabinoside and hydroxyurea, or, for example, one of the preferred anti-metabolites disclosed in European Patent Application No.
  • mitotic inhibitors for example vinblastine
  • alkylating agents for example cis-platin, oxaliplatin, carboplatin and cyclophosphamide
  • anti-metabolites for example 5-fluorouracil, capecitabine, cytosine arabinoside and hydroxyurea, or, for example, one of the preferred anti-metabolites disclosed in European Patent Application No.
  • the compounds described herein may be used alone or in combination with one or more of a variety of anti-cancer agents or supportive care agents.
  • the compounds described herein may be used with cytotoxic agents, e.g., one or more selected from the group consisting of a camptothecin, irinotecan HCl (Camptosar), edotecarin, SU-11248, epirubicin (Ellence), docetaxel (Taxotere), paclitaxel, rituximab (Rituxan) bevacizumab (Avastin), imatinib mesylate (Gleevac), Erbitux, gefitinib (Iressa), and combinations thereof.
  • cytotoxic agents e.g., one or more selected from the group consisting of a camptothecin, irinotecan HCl (Camptosar), edotecarin, SU-11248, epirubicin (Ellence), docetaxe
  • Some embodiments also contemplate the use of the compounds described herein together with hormonal therapy, e.g., exemestane (Aromasin), Lupron, anastrozole (Arimidex), tamoxifen citrate (Nolvadex), Trelstar, and combinations thereof.
  • hormonal therapy e.g., exemestane (Aromasin), Lupron, anastrozole (Arimidex), tamoxifen citrate (Nolvadex), Trelstar, and combinations thereof.
  • some embodiments provide a compound described herein alone or in combination with one or more supportive care products, e.g., a product selected from the group consisting of Filgrastim (Neupogen), ondansetron (Zofran), Fragmin, Procrit, Aloxi, Emend, or combinations thereof.
  • Such conjoint treatment may be achieved by way of the simultaneous, sequential or separate dosing of the individual components of the treatment.
  • the compounds described herein may be used with antitumor agents, alkylating agents, antimetabolites, antibiotics, plant-derived antitumor agents, camptothecin derivatives, tyrosine kinase inhibitors, antibodies, interferons, and/or biological response modifiers.
  • antitumor agents alkylating agents, antimetabolites, antibiotics, plant-derived antitumor agents, camptothecin derivatives, tyrosine kinase inhibitors, antibodies, interferons, and/or biological response modifiers.
  • secondary agents that may be used with the compounds described herein.
  • Alkylating agents include, but are not limited to, nitrogen mustard N-oxide, cyclophosphamide, ifosfamide, melphalan, busulfan, mitobronitol, carboquone, thiotepa, ranimustine, nimustine, temozolomide, AMD-473, altretamine, AP-5280, apaziquone, brostallicin, bendamustine, carmustine, estramustine, fotemustine, glufosfamide, ifosfamide, KW-2170, mafosfamide, and mitolactol; platinum-coordinated alkylating compounds include but are not limited to, cisplatin, carboplatin, eptaplatin, lobaplatin, nedaplatin, oxaliplatin or satrplatin.
  • Antimetabolites include but are not limited to, methotrexate, 6-mercaptopurine riboside, mercaptopurine, 5-fluorouracil (5-FU) alone or in combination with leucovorin, tegafur, UFT, doxifluridine, carmofur, cytarabine, cytarabine ocfosfate, enocitabine, S-1, gemcitabine, fludarabin, 5-azacitidine, capecitabine, cladribine, clofarabine, decitabine, eflornithine, ethynylcytidine, cytosine arabinoside, hydroxyurea, TS-1, melphalan, nelarabine, nolatrexed, ocfosfate, disodium premetrexed, pentostatin, pelitrexol, raltitrexed, triapine, trimetrexate, vidarabine, vincri
  • Antibiotics include but are not limited to: aclarubicin, actinomycin D, amrubicin, annamycin, bleomycin, daunorubicin, doxorubicin, elsamitrucin, epirubicin, galarubicin, idarubicin, mitomycin C, nemorubicin, neocarzinostatin, peplomycin, pirarubicin, rebeccamycin, stimalamer, streptozocin, valrubicin or zinostatin.
  • Hormonal therapy agents e.g., exemestane (Aromasin), Lupron, anastrozole (Arimidex), doxercalciferol, fadrozole, formestane, anti-estrogens such as tamoxifen citrate (Nolvadex) and fulvestrant, Trelstar, toremifene, raloxifene, lasofoxifene, letrozole (Femara), or anti-androgens such as bicalutamide, flutamide, mifepristone, nilutamide, Casodex® (4′-cyano-3-(4-fluorophenylsulphonyl)-2-hydroxy-2-methyl-3′-(trifluoromethyl)propionanilide) and combinations thereof.
  • Plant derived anti-tumor substances include for example those selected from mitotic inhibitors, for example vinblastine, docetaxel (Taxotere) and paclitaxel.
  • Cytotoxic topoisomerase inhibiting agents include one or more agents selected from the group consisting of aclarubicn, amonafide, belotecan, camptothecin, 10-hydroxycamptothecin, 9-aminocamptothecin, diflomotecan, irinotecan HCl (Camptosar), edotecarin, epirubicin (Ellence), etoposide, exatecan, gimatecan, lurtotecan, mitoxantrone, pirarubicin, pixantrone, rubitecan, sobuzoxane, SN-38, tafluposide, and topotecan, and combinations thereof.
  • Interferons include interferon alpha, interferon alpha-2a, interferon, alpha-2b, interferon beta, interferon gamma-1a or interferon gamma-n1.
  • agents include PF3512676, filgrastim, lentinan, sizofilan, TheraCys, ubenimex, WF-10, aldesleukin, alemtuzumab, BAM-002, dacarbazine, daclizumab, denileukin, gemtuzumab ozogamicin, ibritumomab, imiquimod, lenograstim, lentinan, melanoma vaccine (Corixa), molgramostim, OncoVAX-CL, sargramostim, tasonermin, tecleukin, thymalasin, tositumomab, Virulizin, Z-100, epratuzumab, mitumomab, oregovomab, pemtumomab, Provenge.
  • Biological response modifiers are agents that modify defense mechanisms of living organisms or biological responses, such as survival, growth, or differentiation of tissue cells to direct them to have anti-tumor activity.
  • agents include krestin, lentinan, sizofiran, picibanil, or ubenimex.
  • anticancer agents include alitretinoin, ampligen, atrasentan bexarotene, bortezomib. Bosentan, calcitriol, exisulind, finasteride, fotemustine, ibandronic acid, miltefosine, mitoxantrone, I-asparaginase, procarbazine, dacarbazine, hydroxycarbamide, pegaspargase, pentostatin, tazarotne, TLK-286, Velcade, Tarceva, or tretinoin.
  • anti-angiogenic compounds include acitretin, fenretinide, thalidomide, zoledronic acid, angiostatin, aplidine, cilengtide, combretastatin A-4, endostatin, halofuginone, rebimastat, removab, Revlimid, squalamine, ukrain and Vitaxin.
  • Platinum-coordinated compounds include but are not limited to, cisplatin, carboplatin, nedaplatin, or oxaliplatin.
  • Camptothecin derivatives include but are not limited to camptothecin, 10-hydroxycamptothecin, 9-aminocamptothecin, irinotecan, SN-38, edotecarin, and topotecan.
  • Tyrosine kinase inhibitors include, for example, Iressa and SU5416.
  • Antibodies include, for example, Herceptin, Erbitux, Avastin, and Rituximab.
  • Interferons include, for example, interferon alpha, interferon alpha-2a, interferon, alpha-2b, interferon beta, interferon gamma-1a and interferon gamma-n1.
  • Biological response modifiers include agents that modify defense mechanisms of living organisms or biological responses, such as survival, growth, or differentiation of tissue cells to direct them to have anti-tumor activity.
  • agents include, for example, krestin, lentinan, sizofiran, picibanil, and ubenimex.
  • antitumor agents include, for example, mitoxantrone, I-asparaginase, procarbazine, dacarbazine, hydroxycarbamide, pentostatin, and tretinoin. Additionally, PI3K inhibitors and RAS-targeted cancer treatments may be combined with the compounds described herein.
  • Some embodiments also relate to a pharmaceutical composition
  • a pharmaceutical composition comprising a compound of formula (I), formula (II), formula (III), formula (IV), formula (IVa), or formula (IVb), or a pharmaceutically acceptable salt or solvate thereof, as hereinbefore defined in association with a pharmaceutically acceptable adjuvant, diluent or carrier.
  • compositions which comprises mixing a compound of formula (I), formula (II), formula (III), formula (IV), formula (IVa), or formula (IVb), or a pharmaceutically acceptable salt or solvate thereof, as hereinbefore defined with a pharmaceutically acceptable adjuvant, diluent or carrier.
  • the daily dosage of the compound formula (I), formula (II), formula (III), formula (IV), formula (IVa), or formula (IVb), or pharmaceutically acceptable salt thereof may be in the range from 1 mg to 1 gram, preferably 1 mg to 250 mg, more preferably 10 mg to 100 mg.
  • the present embodiments also encompass sustained release compositions.
  • Administration of the compounds descrbed herein can be effected by any method that enables delivery of the compounds to the site of action. These methods include oral routes, intraduodenal routes, parenteral injection (including intravenous, subcutaneous, intramuscular, intravascular or infusion), topical, and rectal administration.
  • the active compound may be applied as a sole therapy or may involve one or more other anti-tumor substances, for example those selected from, for example, mitotic inhibitors, for example vinblastine; alkylating agents, for example cis-platin, carboplatin and cyclophosphamide; anti-metabolites, for example 5-fluorouracil, cytosine arabinoside and hydroxyurea, or, for example, one of the preferred anti-metabolites disclosed in European Patent Application No.
  • mitotic inhibitors for example vinblastine
  • alkylating agents for example cis-platin, carboplatin and cyclophosphamide
  • anti-metabolites for example 5-fluorouracil, cytosine arabinoside and hydroxyurea, or, for example, one of the preferred anti-metabolites disclosed in European Patent Application No.
  • the pharmaceutical composition may, for example, be in a form suitable for oral administration as a tablet, capsule, pill, powder, sustained release formulations, solution, suspension, for parenteral injection as a sterile solution, suspension or emulsion, for topical administration as an ointment or cream or for rectal administration as a suppository.
  • the pharmaceutical composition may be in unit dosage forms suitable for single administration of precise dosages.
  • the pharmaceutical composition will include a conventional pharmaceutical carrier or excipient and a compound described herein as an active ingredient. In addition, it may include other medicinal or pharmaceutical agents, carriers, adjuvants, etc.
  • Exemplary parenteral administration forms include solutions or suspensions of active compounds in sterile aqueous solutions, for example, aqueous propylene glycol or dextrose solutions. Such dosage forms can be suitably buffered, if desired.
  • Suitable pharmaceutical carriers include inert diluents or fillers, water and various organic solvents.
  • the pharmaceutical compositions may, if desired, contain additional ingredients such as flavorings, binders, excipients and the like.
  • excipients such as citric acid
  • disintegrants such as starch, alginic acid and certain complex silicates
  • binding agents such as sucrose, gelatin and acacia.
  • lubricating agents such as magnesium stearate, sodium lauryl sulfate and talc are often useful for tableting purposes.
  • Solid compositions of a similar type may also be employed in soft and hard filled gelatin capsules.
  • Preferred materials include lactose or milk sugar and high molecular weight polyethylene glycols.
  • the active compound therein may be combined with various sweetening or flavoring agents, coloring matters or dyes and, if desired, emulsifying agents or suspending agents, together with diluents such as water, ethanol, propylene glycol, glycerin, or combinations thereof.
  • salt forms were occasionally isolated as a consequence of the mobile phase additives during HPLC based chromatographic purification.
  • salts such as formate, trifluorooacetate and acetate were isolated and tested without further processing. It will be recognized that one of ordinary skill in the art will be able to realize the free base form by standard methodology (such as using ion exchange columns, or performing simple basic extractions using a mild aqueous base).
  • the compounds described herein may be prepared by processes known in the chemical arts, particularly in light of the description contained herein. Certain processes for the manufacture of the compounds described herein are provided as further features of the embodiments and are illustrated in the reaction schemes provided below and in the experimental section.
  • the mono-ester mono-acid A-1 which may be obtained either from commercial sources, or from selective ester hydrolysis or desymmetrization of symmetrical anhydrides under standard literature conditions (see for example, J. Am. Chem. Soc., 2000, 122, 9542 and Helv. Chim. Acta., 1983, 66, 2501), is subjected to selective reduction of the carboxylic acid moiety using a reducing agent such as borane.dimethylsulfide to afford A-2.
  • a reducing agent such as borane.dimethylsulfide
  • the alcohol in A-2 may be halogenated to form an alkyl halide such as an iodide or a bromide using reagents such as iodine/triphenylphosphine in the presence of a base such as imidazole or carbon tetrabromide to afford A-3.
  • the coupling partner A-5 is obtained from the acylation of a commercially available 2-amino-6-halogenated heterocycle, A-4, using an acid in the presence of a standard coupling reagent such as HATU or HBTU in the presence of a base such as Hunig's base or triethylamine.
  • the reaction between A-5 and A-3 takes place through a palladium-mediated process such as a Negishi reaction.
  • the halogenated compound A-3 may be activated as an organometallic species such as an organozincate by treatment with species such as zinc dust in the presence of an activating agent such a 1,2-dibromoethane and TMSCl in a solvent such as DMF, or without activation by using diethyl zinc for the metallation process.
  • the zincate obtained may be coupled with the halogenated heterocycle A-5 through a Negishi reaction using a palladium catalyst such as Pd 2 (dba) 3 in the presence of a suitable ligand such as tri(o-tolylphoshine) in a solvent such as DMF to afford A-6.
  • the ester in A-6 is hydrolyzed by an inorganic base such as lithium hydroxide or sodium hydroxide in a solvent such as methanol and water to afford the carboxylic acid A-7.
  • Condensation of A-7 with thiosemicarbazide in the presence of phosphorus oxychloride as both an activating and dehydrating agent provides the aminothiadiazole A-8.
  • Acylation of A-8 either using by reaction with an acid chloride or by using a suitable amide coupling agent (such as T3P, HATU or HBTU) and an appropriate carboxylic acid in the presence of a base such as pyridine, TEA or Hunig's base in a solvent such as DMF or DMA affords A-9.
  • Separation of the enantiomers may be carried out under standard methods known in the art such as chiral SFC or HPLC to afford the single enantiomer A-9.
  • the di-acid B-1 may be either obtained from commercial sources, or prepared by methods, which are established in the literature or reported herein. Condensation of B-1 with thiosemicarbazide in the presence of phosphorus oxychloride as both an activating and dehydrating agent provides the bis-aminothiadiazole B-2.
  • B-2 either by reaction with an acid chloride or by using a suitable amide coupling agent (such as T3P, HATU or HBTU) and an appropriate carboxylic acid in the presence of a base such as pyridine, TEA or Hunig's base in a solvent such as DMF or DMA affords the symmetrically substituted bis-aminothidiazole, B-3.
  • a suitable amide coupling agent such as T3P, HATU or HBTU
  • a base such as pyridine, TEA or Hunig's base in a solvent such as DMF or DMA
  • Separation of the enantiomers may be carried out under standard methods known in the art such as chiral SFC or HPLC to afford single enantiomers of
  • the mono-ester mono-acid (A-1 in scheme A) is converted into the mono-thiadiazole under standard conditions known in the art such as condensation with thiosemicarbazide in the presence of an activating/dehydrating agent such as phosphorus oxychloride to provide C-1.
  • Acylation of C-1 is carried out under standard conditions such as condensation with acetyl chloride or acetic anhydride in the presence of a base such as triethylamine in a solvent such as DMF to afford C-2.
  • Ester hydrolysis of C-2 is carried out under basic conditions using a base such as NaOH or LiOH in a solvent such as methanol to afford C-3.
  • C-4 Condensation of C-3 with hydrazine in the presence of a suitable coupling agent (such as T3P, HBTU or HATU) and a base (such as pyridine, TEA or DIPEA) in a suitable solvent such as DMF affords C-4.
  • a suitable solvent such as DMF
  • C-4 Reaction with C-4 with an isothiocyanate in a suitable solvent such as ethyl acetate, THF or methylene chloride affords C-5.
  • Isothiocyanates are either commercially available or may be prepared by direct reaction of an acid chloride with sodium isothiocyanate under conditions, which are well established in the literature.
  • C-5 is cyclized by dehydration under acidic conditions in the presence of a suitable acid such as sulfuric acid to afford C-8.
  • C-3 is condensed with thiosemicarbazide in the presence of a suitable coupling agent (such as HBTU or HATU) and a base (such as TEA or DIPEA) in a suitable solvent such as DMF to afford C-6.
  • C-6 is cyclized by dehydration under acidic conditions in the presence of a suitable acid such as sulfuric acid to afford C-7.
  • a suitable amide coupling agent such as T3P, HATU or HBTU
  • an appropriate carboxylic acid in the presence of a base such as pyridine, TEA or Hunig's base in a solvent such as DMF or DMA affords C-8.
  • Separation of the enantiomers may be carried out under standard methods known in the art such as chiral SFC or HPLC to afford single enantiomer C-8.
  • the mono-ester mono-acid (A-1 in Scheme A) is converted into the mono-thiadiazole under standard conditions known in the art such as condensation with thiosemicarbazide in the presence of an activating/dehydrating agent such as phosphorus oxychloride to provide D-1.
  • an activating/dehydrating agent such as phosphorus oxychloride
  • D-1 Acylation of D-1 either by reaction with an acid chloride or by using a suitable amide coupling agent (such as T3P, HATU or HBTU) and an appropriate carboxylic acid in the presence of a base such as pyridine, TEA or Hunig's base in a solvent such as DMF or DMA affords D-2.
  • Ester hydrolysis of D-2 is carried out under basic conditions using a base such as NaOH or LiOH in a solvent such as methanol to afford D-3.
  • D-3 is condensed with thiosemicarbazide in the presence of a suitable coupling agent (such as T3P, HBTU or HATU) and a base (such as pyridine, TEA or Hunig's base) in a suitable solvent such as DMF to afford D-4.
  • D-4 is cyclized by dehydration under acidic conditions in the presence of a suitable acid such as sulfuric acid to afford D-5.
  • Acylation of D-5 is carried out under standard conditions using an acylation agent such as acetic anhydride in a solvent such as acetic acid to afford D-6. Separation of the enantiomers may be carried out under standard methods known in the art such as chiral SFC or HPLC to afford single enantiomer D-6.
  • the cyclic keto-acid E-1 may be either obtained from commercial sources, or prepared by methods, which are established in the literature or reported herein.
  • Reaction of the ketone function with an organophosphorane in the presence of a base such as sodium hydride in a solvent such as THF in a Horner-Wittig-Emmons reaction gives the unsaturated ester, E-2.
  • Reduction of the olefin under hydrogen pressure in the presence of a heterogeneous catalyst such as palladium on carbon or platinum oxide in a solvent such as methanol or dichloromethane gives E-3 as a mixture of diastereomers in which reduction from the less hindered face will be preferred.
  • the mono-ester mono-acid A-1 is condensed with the alkyl or aryl-substituted thiosemicarbazide, F-2, in the presence of phosphorus oxychloride as both an activating and dehydrating agent to provide the alkyl or aryl-substituted aminothiadiazole F-3.
  • the alkyl-substituted thiosemicarbazide F-2 is obtained either from commercial sources or by the action of hydrazine on a commercial alkyl or aryl isothiocyanide, F-1 or by using alternative methods which are well established in the literature ( Phosphorus, Sulfur, and Silicon and the Related Elements, 1991, 60 (1-2), 15-19).
  • Hydrolysis of the ester F-3 using an inorganic base such as lithium hydroxide or sodium hydroxide in a solvent such as methanol and water gives the carboxylic acid, F-4.
  • Condensation of F-4 with thiosemicarbazide in the presence of phosphorus oxychloride as both an activating and dehydrating agent provides the bis-aminothiadiazole E-5.
  • Acylation of F-5 either using by reaction with an acid chloride or by using a suitable amide coupling agent (such as T3P, HATU or HBTU) and an appropriate carboxylic acid in the presence of a base such as pyridine, TEA or Hunig's base in a solvent such as DMF or DMA affords the symmetrically substituted bis-aminothidiazole, F-6.
  • a suitable amide coupling agent such as T3P, HATU or HBTU
  • an appropriate carboxylic acid in the presence of a base such as pyridine, TEA or Hunig's base in a solvent such as DMF or DMA affords the symmetrically substituted bis-aminothidiazole, F-6.
  • Separation of the enantiomers
  • the di-acid B-1 may be either obtained from commercial sources, or prepared by methods, which are established in the literature or reported herein.
  • B-1 may be converted to the dihalide G-1 through a decarboxylation-halogenation type sequence typically referred to as a Hunsdiecker reaction, which may take place under photochemical conditions in the presence of a suitable halogen source, such as diiodohydantoin in a solvent such as 1,2-dichloroethane.
  • a suitable halogen source such as diiodohydantoin in a solvent such as 1,2-dichloroethane.
  • the coupling partner A-5 is obtained from the acylation of a commercially available 2-amino-6-halogenated heterocycle, A-4, using an acid in the presence of a standard coupling reagent such as T3P, HATU or HBTU in the presence of a base such as pyridine, Hunig's base or TEA.
  • a standard coupling reagent such as T3P, HATU or HBTU in the presence of a base such as pyridine, Hunig's base or TEA.
  • the reaction between A-5 and B-1 takes place through a palladium-mediated process such as a Negishi reaction.
  • the di-halogenated compound B-1 may be activated as an organometallic species such as an organozincate by treatment with species such as zinc dust in the presence of an activating agent such a 1,2-dibromoethane and TMS-Cl in a solvent such as DMF, or without activation by using diethyl zinc for the metallation process.
  • the zincate obtained may be coupled with the halogenated heterocycle A-5 through a Negishi reaction using a palladium catalyst such as Pd 2 (dba) 3 in the presence of a suitable ligand such as tri(o-tolylphoshine) in a solvent such as DMF to afford G-2.
  • separation of the enantiomers of G-2 may be carried out under standard methods known in the art such as chiral SFC or HPLC to afford the single enantiomers of G-2.
  • coupling partner A-5 is obtained from the acylation of a commercially available 2-amino-6-halogenated heterocycle, A-4, using an acid in the presence of a standard coupling reagent such as T3P, HATU or HBTU in the presence of a base such as pyridine, Hunig's base or TEA.
  • Vinyl boronate H-1 may be obtained from an established literature procedure involving borylation of the corresponding halogenated ⁇ , ⁇ -unsaturated cyclic ketone (US 2012/0077814).
  • the reaction between A-5 and H-1 takes place through a palladium-mediated process such as a Suzuki reaction to give H-2.
  • A-5 and H-1 may be reacted together at elevated temperature in the presence of a palladium catalyst, such as Pd(dppf)Cl 2 in the presence of suitable base (such as K 3 PO 4 or CsF) in a mixed solvent system comprising of an organic solvent (for example, THF, DME or toluene) and water.
  • a palladium catalyst such as Pd(dppf)Cl 2
  • suitable base such as K 3 PO 4 or CsF
  • a mixed solvent system comprising of an organic solvent (for example, THF, DME or toluene) and water.
  • a heterogeneous catalyst such as palladium on carbon or platinum oxide in a solvent such as methanol or dichloromethane gives H-3.
  • H-3 may be elaborated to H-4 through a Horner-Wittig-Emmons type olefination involving treatment of with a phosphonate reagent such as diethyl(cyanomethyl)phosphonate in the presence of a strong base such as NaH in a suitable solvent (for example, THF).
  • a phosphonate reagent such as diethyl(cyanomethyl)phosphonate
  • a strong base such as NaH in a suitable solvent
  • a suitable solvent for example, THF
  • Reduction of the exocyclic olefin of H-4 to give H-5 may be achieved through utilization of a hydride-based reagent.
  • L-Selectride may be employed as the reductant in a solvent such as THF at depressed temperature to provide H-5 as a mixture of diastereomers.
  • H-6 Condensation of H-5 with thiosemicarbazide in the presence of an acid such as TFA at elevated temperature provides the aminothiadiazole H-6.
  • Acylation of H-6 either using by reaction with an acid chloride or by using a suitable amide coupling agent (such as T3P, HATU or HBTU) and an appropriate carboxylic acid in the presence of a base such as pyridine, TEA or Hunig's base in a solvent such as DMF or DMA affords H-7.
  • a suitable amide coupling agent such as T3P, HATU or HBTU
  • an appropriate carboxylic acid in the presence of a base such as pyridine, TEA or Hunig's base in a solvent such as DMF or DMA affords H-7.
  • Separation of the diastereomers and enantiomers may be carried out under standard methods known in the art such as chiral SFC or HPLC to afford the single enantiomers of H-7.
  • any compatible protecting radical may be used.
  • methods of protection and deprotection such as those described by T.W. Greene ( Protective Groups in Organic Synthesis , A. Wiley-Interscience Publication, 1981) or by P. J. Kocienski ( Protecting groups , Georg Thieme Verlag, 1994), may be used.
  • Step 1 Preparation of methyl-(cis)-3-(hydroxymethyl)cyclopentanecarboxylate
  • Step 2 Preparation of methyl-(cis)-3-(iodomethyl)cyclopentanecarboxylate
  • Step 4 Preparation of (cis)-3-( ⁇ 6-[(phenylacetyl)amino]pyridazin-3-yl ⁇ methyl) cyclopentanecarboxylate
  • Step 5 Preparation of (cis)-3-( ⁇ 6-[(phenylacetyl)amino]pyridazin-3-yl ⁇ methyl)cyclopentanecarboxylic acid
  • Step 6 Preparation of N-[6-( ⁇ (cis)-3-[(2-carbamothioylhydrazinyl)carbonyl]cyclopentyl ⁇ methyl)pyridazin-3-yl]-2-phenylacetamide
  • Step 7 Preparation of N-[6- ⁇ [(cis)-3-(5-amino-1,3,4-thiadiazol-2-yl)cyclopentyl]methyl ⁇ pyridazin-3-yl)-2-phenylacetamide
  • N-[6-( ⁇ (cis)-3-[(2-carbamothioylhydrazinyl)carbonyl]cyclopentyl ⁇ methyl)pyridazin-3-yl]-2-phenylacetamide 120 mg, 0.29 mmol was treated with neat sulfuric acid (0.58 mL) at 0° C. After 30 min at 0° C., the reaction mixture was added dropwise to a solution of ice-cold aq. NaHCO 3 . The resulting mixture was extracted with CH 2 Cl 2 four times, and dried over Na 2 SO 4 .
  • Step 8 Preparation of 2-phenyl-N-(6- ⁇ [(cis)-3- ⁇ 5-[(pyridine-2-ylacetyl)amino]-1,3,4-thiadiazol-2-yl ⁇ cyclopentyl]methyl ⁇ pyridazin-3-yl)acetamide
  • Step 1 Preparation of 5-(((1R,3S)-3-(5-amino-1,3,4-thiadiazol-2-yl)cyclopentyl)methyl)-1,3,4-thiadiazol-2-amine
  • Step 2 Preparation of 2-(pyridin-2-yl)-N-(5- ⁇ [(1R,3S)-3- ⁇ 5-[(pyridin-2-ylacetyl)amino]-1,3,4-thiadiazol-2-yl ⁇ cyclopentyl]methyl ⁇ -1,3,4-thiadiazol-2-yl)acetamide
  • the absolute stereochemistry of the final compounds was determined by processing the racemic (cis)-di-acid through the identical chemical sequence as described below.
  • Step 1 Preparation of 5-(((cis)-3-(5-amino-1,3,4-thiadiazol-2-yl)cyclopentyl)methyl)-1,3,4-thiadiazol-2-amine
  • Cis-3-(carboxymethyl)cyclopentane carboxylic acid (12.0 g, 63.89 mmol) and thiosemicarbazide (11.64 g, 127.77 mmol) were combined and POCl 3 (80 mL) was added.
  • the reaction mixture was heated at 100° C. for 3 hr to give a yellow solution, which was then cooled to room temperature.
  • the crude was quenched in warm water and basified to pH 7 with NaOH 50%. The resulting solid was filtered off, washed well with water and dried at 60° C.
  • Step 2 Preparation of 2-(pyridin-2-yl)-N-(5- ⁇ [(1R,3S)-3- ⁇ 5-[(pyridin-2-ylacetyl)amino]-1,3,4-thiadiazol-2-yl ⁇ cyclopentyl]methyl ⁇ -1,3,4-thiadiazol-2-yl)acetamide
  • Example 4 Crystals of Example 4 were grown by vapor diffusion of ether into an 80/20 dichloromethane/methanol solution, and were subjected to single crystal X-ray diffraction studies to obtain the absolute stereochemistry of the cyclopentane ring junction.
  • Example 4 was shown to be 2-(pyridin-2-yl)-N-(5- ⁇ [(1S,3R)-3- ⁇ 5-[(pyridin-2-ylacetyl)amino]-1,3,4-thiadiazol-2-yl ⁇ cyclopentyl]methyl ⁇ -1,3,4-thiadiazol-2-yl)acetamide, thus enabling the assignment of Example 2 as 2-(pyridin-2-yl)-N-(5- ⁇ [(1R,3S)-3- ⁇ 5-[(pyridin-2-ylacetyl)amino]-1,3,4-thiadiazol-2-yl ⁇ cyclopentyl]methyl ⁇ -1,3,4-thiadiazol-2-yl)acetamide.
  • Example 6 After being dissolved in hot DMSO (2 mL), the compound was purified via reverse-phase chromatography, eluting with 5-100% MeCN in 0.1% aq. formic acid to provide racemic Example 6 as a colorless solid (38 mg, 15% yield).
  • Step 1 Preparation of methyl [(cis)-3-(5-amino-1,3,4-thiadiazol-2-yl)cyclopentyl]acetate
  • Step 2 Preparation of methyl ⁇ (cis)-3-[5-(acetylamino)-1,3,4-thiadiazol-2-yl]cyclopentyl ⁇ acetate
  • Step 3 Preparation of ⁇ (cis)-3-[5-(acetylamino)-1,3,4-thiadiazol-2-yl]cyclopentyl ⁇ acetic acid
  • Step 4 Preparation of N- ⁇ 5-[(cis)-3-(2-hydrazinyl-2-oxoethyl)cyclopentyl]-1,3,4-thiadiazol-2-yl ⁇ acetamide
  • Step 5 Preparation of N- ⁇ [2-( ⁇ (cis)-3-[5-(acetylamino)-1,3,4-thiadiazol-2-yl]cyclopentyl ⁇ acetyl)hydrazinyl]carbonothioyl ⁇ benzamide
  • Step 6 Preparation of N-[5-( ⁇ (cis)-3-[5-(acetylamino)-1,3,4-thiadiazol-2-yl]cyclopentyl ⁇ methyl)-1,3,4-thiadiazol-2-yl]benzamide (Example 11)
  • N- ⁇ [2-( ⁇ (cis)-3-[5-(acetylamino)-1,3,4-thiadiazol-2-yl]cyclopentyl ⁇ acetyl)hydrazinyl]carbonothioyl ⁇ benzamide (58 mg, 0.13 mmol) was stirred in ice cold sulfuric acid (3 mL) for 3 hr. The clear solution was slowly added to ice cold water (10 mL) giving an oily suspension. EtOAc (10 mL) was added and the mixture stirred giving a cream solid.
  • Step 1 Preparation of N- ⁇ [2-( ⁇ (cis)-3-[5-(acetylamino)-1,3,4-thiadiazol-2-yl]cyclopentyl ⁇ acetyl)hydrazinyl]carbonothioyl ⁇ -2-phenylacetamide
  • step 4 N- ⁇ 5-[(cis)-3-(2-hydrazinyl-2-oxoethyl)cyclopentyl]-1,3,4-thiadiazol-2-yl ⁇ acetamide (100 mg, 0.353 mmol) in EtOAc (2 mL) was added phenylacetyl isothiocyanate (75 mg, 0.424 mmol) and the suspension stirred at 40° C. for 3 hr. The mixture was cooled and filtered under vacuum.
  • Step 2 Preparation of N-[5-( ⁇ (cis)-3-[5-(acetylamino)-1,3,4-thiadiazol-2-yl]cyclopentyl ⁇ methyl)-1,3,4-thiadiazol-2-yl]-2-phenylacetamide (Example 14)
  • Step 1 Preparation of N-(5- ⁇ (cis)-3-[2-(2-carbamothioylhydrazinyl)-2-oxoethyl]cyclopentyl ⁇ -1,3,4-thiadiazol-2-yl)acetamide
  • Step 2 Preparation of N-(5- ⁇ (cis)-3-[(5-amino-1,3,4-thiadiazol-2-yl)methyl]cyclopentyl ⁇ -1,3,4-thiadiazol-2-yl)acetamide
  • N-(5- ⁇ (cis)-3-[2-(2-carbamothioylhydrazinyl)-2-oxoethyl]cyclopentyl ⁇ -1,3,4-thiadiazol-2-yl)acetamide (671 mg, 1.96 mmol) was stirred in ice cold sulfuric acid (3 mL) for 3 hr. The clear solution was slowly added to an ice cold aqueous solution of NaHCO 3 to adjust to pH ⁇ 8 (Caution—vigorous gas evolution).
  • Step 3 Preparation of N-[5-( ⁇ (1R,3S)-3-[5-(acetylamino)-1,3,4-thiadiazol-2-yl]cyclopentyl ⁇ methyl)-1,3,4-thiadiazol-2-yl]-2-(pyridin-2-yl)acetamide (Example 17)
  • Step 1 Preparation of methyl 2-((cis)-3-(5-(2-pyrimidin-4-yl)acetamino)-1,3,4-thiadiazol-2yl)cyclopentyl)acetate
  • Step 2 Preparation of 2-((cis)-3-(5-(2-pyrimidin-4-yl)acetamino)-1,3,4-thiadiazol-2yl)cyclopentyl)acetic acid
  • Methyl-2-((cis)-3-(5-(2-pyrimidin-4-yl)acetamino)-1, 3,4-thiadiazol-2-yl)-cyclopentyl)acetate (1.27 g, 3.52 mmol) was dissolved in a mixture of MeOH (20 mL) and water (10 mL). Then, LiOH (674 mg, 28.2 mmol) was added to the methyl ester at room temperature, and stirred for 2 hr. The reaction mixture was evaporated to remove MeOH and the resulting mixture was diluted with water. Then, the crude was washed with EtOAc and the aq. layer was acidified with 1 N HCl to pH ⁇ 3.
  • Step 3 Preparation of N-(5-((cis)-3-(2-(2-carbamothioylhydrazinyl)-2-oxoethyl)cyclopentyl)-1,3,4-thiadiazol-2yl)-2-(pyrimidin-4-yl)acetamide
  • Step 4 Preparation of N-(5-((cis)-3-((5-amino-1,3,4-thiadiazol-2-yl)-methyl)cyclopentyl)-1,3,4-thiadiazol-2-yl)-2-(pyrimidin-4-yl)acetamide
  • N-(5-((cis)-3-(2-(2-carbamothioylhydrazinyl)-2-oxoethyl)cyclopentyl)-1, 3,4-thiadiazol-2yl)-2-(pyrimidin-4-yl)acetamide was treated with neat sulfuric acid at 0° C. After 3 hr at 0° C., the reaction mixture was added dropwise to an ice-cold aq. NaHCO 3 solution.
  • Step 5 Preparation of N- ⁇ 5-[(cis)-3- ⁇ [5-(acetylamino)-1,3,4-thiadiazol-2-yl]methyl ⁇ cyclopentyl]-1, 3,4-thiadiazol-2-yl ⁇ -2-(pyrimidin-4-yl)acetamide (Example 20)
  • N-(5-((cis)-3-((5-amino-1,3,4-thiadiazol-2-yl)methyl)cyclopentyl)-1,3,4-thiadiazol-2-yl)-2-(pyrimidin-4-yl)acetamide (118 mg, 0.293 mmol) was dissolved in AcOH (1 mL) and treated with Ac 2 O (56 ⁇ L, 0.586 mmol) at room temperature.
  • reaction mixture was purified by reverse phase chromatography eluting with MeCN:water (5:95 to 95:5) to give racemic N- ⁇ 5-[(cis)-3- ⁇ [5-(acetylamino)-1,3,4-thiadiazol-2-yl]methyl ⁇ cyclopentyl]-1,3,4-thiadiazol-2-yl ⁇ -2-(pyrimidin-4-yl)acetamide as an orange solid (26 mg, 20%).
  • Step 1 Preparation of 5- ⁇ [3-(5-amino-1,3,4-thiadiazol-2-yl)cyclobutyl]methyl ⁇ -1,3,4-thiadiazol-2-amine
  • Step 2 Preparation of 2-(pyridin-2-yl)-N- ⁇ 5-[(cis-3- ⁇ 5-[(pyridin-2-ylacetyl)amino]-1,3,4-thiadiazol-2-yl ⁇ cyclobutyl)methyl]-1,3,4-thiadiazol-2-yl ⁇ acetamide (Example 22) and 2-(pyridin-2-yl)-N- ⁇ 5-[(cis-3- ⁇ 5-[(pyridin-2-ylacetyl)amino]-1,3,4-thiadiazol-2-yl ⁇ cyclobutyl)methyl]-1,3,4-thiadiazol-2-yl ⁇ acetamide (Example 23)
  • the cis and trans isomers were separated by SFC to afford both diastereomers.
  • Step 1 Preparation of methyl ⁇ 3-[(cis)-5-(ethylamino)-1,3,4-thiadiazol-2-yl]cyclopentyl ⁇ acetate
  • 3-(2-methoxy-2-oxoethyl)-cyclopentanecarboxylic acid 500 mg, 2.68 mmol
  • 4-ethyl-3-thiosemicarbazide 320 mg, 2.68 mmol
  • the mixture was allowed to cool, evaporated in vacuo, and then azeotoped three times with toluene to remove POCl 3 residues.
  • the resulting amber oil was carefully quenched with saturated NaHCO 3 solution (100 mL), and then extracted into EtOAc (3 ⁇ 50 mL).
  • Step 2 Preparation of ⁇ (cis)-3-[5-(ethylamino)-1,3,4-thiadiazol-2-yl]cyclopentyl ⁇ acetic acid
  • Step 3 Preparation of 5- ⁇ (cis)-3-[(5-amino-1,3,4-thiadiazol-2-yl)methyl]cyclopentyl ⁇ -N-ethyl-1,3,4-thiadiazol-2-amine

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* Cited by examiner, † Cited by third party
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CN116023375A (zh) * 2021-10-25 2023-04-28 成都苑东生物制药股份有限公司 一种杂环类衍生物、其制备方法及用途

Families Citing this family (3)

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Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20140142081A1 (en) * 2012-11-22 2014-05-22 Agios Pharmaceuticals, Inc Compounds and their methods of use

Family Cites Families (78)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2037257A1 (en) 1970-07-28 1972-02-03 Farbwerke Hoechst AG, vorm. Meister Lucius & Brüning, 6000 Frankfurt Poly-(5-amino-1,3,4-thiadiazol-2-yl) derivs prepn - intermediates for drug and polymer prodn
GB8607683D0 (en) 1986-03-27 1986-04-30 Ici Plc Anti-tumor agents
GB8827305D0 (en) 1988-11-23 1988-12-29 British Bio Technology Compounds
WO1992020642A1 (en) 1991-05-10 1992-11-26 Rhone-Poulenc Rorer International (Holdings) Inc. Bis mono-and bicyclic aryl and heteroaryl compounds which inhibit egf and/or pdgf receptor tyrosine kinase
NZ243082A (en) 1991-06-28 1995-02-24 Ici Plc 4-anilino-quinazoline derivatives; pharmaceutical compositions, preparatory processes, and use thereof
FI941572A7 (fi) 1991-10-07 1994-05-27 Oncologix Inc Anti-erbB-2-monoklonaalisten vasta-aineiden yhdistelmä ja käyttömenete lmä
AU661533B2 (en) 1992-01-20 1995-07-27 Astrazeneca Ab Quinazoline derivatives
ATE503496T1 (de) 1992-02-06 2011-04-15 Novartis Vaccines & Diagnostic Biosynthetisches bindeprotein für tumormarker
US6177401B1 (en) 1992-11-13 2001-01-23 Max-Planck-Gesellschaft Zur Forderung Der Wissenschaften Use of organic compounds for the inhibition of Flk-1 mediated vasculogenesis and angiogenesis
GB9323290D0 (en) 1992-12-10 1994-01-05 Zeneca Ltd Quinazoline derivatives
US5455258A (en) 1993-01-06 1995-10-03 Ciba-Geigy Corporation Arylsulfonamido-substituted hydroxamic acids
GB9314884D0 (en) 1993-07-19 1993-09-01 Zeneca Ltd Tricyclic derivatives
GB9314893D0 (en) 1993-07-19 1993-09-01 Zeneca Ltd Quinazoline derivatives
IL112248A0 (en) 1994-01-25 1995-03-30 Warner Lambert Co Tricyclic heteroaromatic compounds and pharmaceutical compositions containing them
GB9510757D0 (en) 1994-09-19 1995-07-19 Wellcome Found Therapeuticaly active compounds
GB9424233D0 (en) 1994-11-30 1995-01-18 Zeneca Ltd Quinazoline derivatives
US5863949A (en) 1995-03-08 1999-01-26 Pfizer Inc Arylsulfonylamino hydroxamic acid derivatives
US5702637A (en) 1995-04-19 1997-12-30 Minnesota Mining And Manufacturing Company Liquid crystal compounds having a chiral fluorinated terminal portion
US5861510A (en) 1995-04-20 1999-01-19 Pfizer Inc Arylsulfonyl hydroxamic acid derivatives as MMP and TNF inhibitors
US5880141A (en) 1995-06-07 1999-03-09 Sugen, Inc. Benzylidene-Z-indoline compounds for the treatment of disease
JPH09104838A (ja) 1995-10-09 1997-04-22 Mitsui Toatsu Chem Inc 水性塗料用樹脂組成物
GB9520822D0 (en) 1995-10-11 1995-12-13 Wellcome Found Therapeutically active compounds
GB9624482D0 (en) 1995-12-18 1997-01-15 Zeneca Phaema S A Chemical compounds
PT780386E (pt) 1995-12-20 2003-02-28 Hoffmann La Roche Inibidores de metaloprotease de matriz
GB9603095D0 (en) 1996-02-14 1996-04-10 Zeneca Ltd Quinazoline derivatives
IL125954A (en) 1996-03-05 2003-06-24 Zeneca Ltd Quinazoline derivatives, processes for their preparation, pharmaceutical compositions containing them and use thereof in the manufacture of medicaments having an antiangiogenic and/or vascular permeability reducing effect
ATE227283T1 (de) 1996-07-13 2002-11-15 Glaxo Group Ltd Kondensierte heterozyklische verbindungen als protein kinase inhibitoren
HRP970371A2 (en) 1996-07-13 1998-08-31 Kathryn Jane Smith Heterocyclic compounds
AU3693697A (en) 1996-07-13 1998-02-09 Glaxo Group Limited Bicyclic heteroaromatic compounds as protein tyrosine kinase inhibitors
CN1225639A (zh) 1996-07-18 1999-08-11 美国辉瑞有限公司 基于次膦酸酯的基质金属蛋白酶抑制剂
SK21499A3 (en) 1996-08-23 2000-05-16 Pfizer Arylsulfonylamino hydroxamic acid derivatives
EP0950059B1 (en) 1997-01-06 2004-08-04 Pfizer Inc. Cyclic sulfone derivatives
SK283963B6 (sk) 1997-02-03 2004-06-08 Pfizer Products Inc. Deriváty arylsulfonylaminohydroxamovej kyseliny, farmaceutický prostriedok, spôsob inhibície matričných metaloproteináz alebo produkcie faktora nekrózy nádorov
WO1998034915A1 (en) 1997-02-07 1998-08-13 Pfizer Inc. N-hydroxy-beta-sulfonyl-propionamide derivatives and their use as inhibitors of matrix metalloproteinases
JP3710489B2 (ja) 1997-02-11 2005-10-26 ファイザー・インク アリールスルホニルヒドロキサム酸誘導体
WO1998050356A1 (en) 1997-05-07 1998-11-12 Sugen, Inc. 2-indolinone derivatives as modulators of protein kinase activity
WO1998054093A1 (en) 1997-05-30 1998-12-03 Merck & Co., Inc. Novel angiogenesis inhibitors
DE69838172T2 (de) 1997-08-22 2008-04-10 Astrazeneca Ab Oxindolylchinazolinderivate als angiogenesehemmer
WO1999016755A1 (en) 1997-09-26 1999-04-08 Merck & Co., Inc. Novel angiogenesis inhibitors
JP2001522853A (ja) 1997-11-11 2001-11-20 ファイザー・プロダクツ・インク 抗癌剤として有用なチエノピリミジンおよびチエノピリジン誘導体
GB9725782D0 (en) 1997-12-05 1998-02-04 Pfizer Ltd Therapeutic agents
RS49779B (sr) 1998-01-12 2008-06-05 Glaxo Group Limited, Biciklična heteroaromatična jedinjenja kao inhibitori protein tirozin kinaze
GB9800575D0 (en) 1998-01-12 1998-03-11 Glaxo Group Ltd Heterocyclic compounds
GB9801690D0 (en) 1998-01-27 1998-03-25 Pfizer Ltd Therapeutic agents
PA8469501A1 (es) 1998-04-10 2000-09-29 Pfizer Prod Inc Hidroxamidas del acido (4-arilsulfonilamino)-tetrahidropiran-4-carboxilico
PA8469401A1 (es) 1998-04-10 2000-05-24 Pfizer Prod Inc Derivados biciclicos del acido hidroxamico
TR200003514T2 (tr) 1998-05-29 2002-05-21 Sugen Inc. Pirol ikame edilmiş 2-indolinon protein kinaz inhibitörleri
UA71945C2 (en) 1999-01-27 2005-01-17 Pfizer Prod Inc Substituted bicyclic derivatives being used as anticancer agents
JP3270834B2 (ja) 1999-01-27 2002-04-02 ファイザー・プロダクツ・インク 抗がん剤として有用なヘテロ芳香族二環式誘導体
EP1292591B1 (en) 2000-06-22 2005-02-02 Pfizer Products Inc. Substituted bicyclic derivatives for the treatment of abnormal cell growth
US6451828B1 (en) 2000-08-10 2002-09-17 Elan Pharmaceuticals, Inc. Selective inhibition of glutaminase by bis-thiadiazoles
AR042586A1 (es) 2001-02-15 2005-06-29 Sugen Inc 3-(4-amidopirrol-2-ilmetiliden)-2-indolinona como inhibidores de la protein quinasa; sus composiciones farmaceuticas; un metodo para la modulacion de la actividad catalitica de la proteinquinasa; un metodo para tratar o prevenir una afeccion relacionada con la proteinquinasa
DE10109807A1 (de) 2001-03-01 2002-09-05 Wella Ag Verbrückte Diaminopyrazole und diese Verbindungen enthaltende Färbemittel
US7029729B2 (en) 2003-02-24 2006-04-18 3M Innovative Properties Company Cholesteric liquid crystal additives
ES2279446T3 (es) 2003-08-15 2007-08-16 MERCK & CO., INC. Antagonistas nmda/nr2b de 4-cicloalquilaminopirazolo pirimidina.
WO2006028269A2 (en) 2004-09-09 2006-03-16 Astellas Pharma Inc. Thiazole derivatives having vap-1 ihibitory activity
EP2137158A4 (en) 2007-02-28 2012-04-18 Methylgene Inc LOW-MOLECULAR INHIBITORS OF PROTEINARGININE METHYLTRANSFERASES (PRMTS)
US20120077814A1 (en) 2010-09-10 2012-03-29 Zhong Wang Sulfonamide, sulfamate, and sulfamothioate derivatives
US8604016B2 (en) 2011-11-21 2013-12-10 Calithera Biosciences Inc. Heterocyclic inhibitors of glutaminase
CN104220070B (zh) * 2011-11-21 2020-01-21 卡利泰拉生物科技公司 谷氨酰胺酶的杂环抑制剂
US9665874B2 (en) 2012-03-13 2017-05-30 American Express Travel Related Services Company, Inc. Systems and methods for tailoring marketing
WO2014031933A2 (en) 2012-08-24 2014-02-27 Philip Jones Heterocyclic modulators of hif activity for treatment of disease
SMT202100589T1 (it) * 2012-11-16 2021-11-12 Calithera Biosciences Inc Inibitori di glutaminasi eterociclici
US10011574B2 (en) 2012-11-21 2018-07-03 Agios Pharmaceuticals, Inc. Glutaminase inhibitors and method of use
WO2014079011A1 (en) * 2012-11-22 2014-05-30 Agios Pharmaceuticals, Inc. Heterocyclic compounds for inhibiting glutaminase and their methods of use
JP6285950B2 (ja) 2012-12-03 2018-02-28 キャリセラ バイオサイエンシーズ， インコーポレイテッド グルタミナーゼの複素環式阻害剤を用いるがんの処置
US9868705B2 (en) * 2013-09-27 2018-01-16 The Board Of Trustees Of The University Of Illinois Tetra-aryl cyclobutane inhibitors of androgen receptor action for the treatment of hormone refractory cancer
WO2015061432A1 (en) 2013-10-25 2015-04-30 Calithera Biosciences, Inc. Treatment of viral infections with inhibitors of glutaminase
JP6783663B2 (ja) * 2014-01-06 2020-11-11 ライゼン・ファーマシューティカルズ・エスアー 新規グルタミナーゼ阻害剤
EP3116872A4 (en) 2014-03-14 2017-08-30 Calithera Biosciences, Inc. Combination therapy with glutaminase inhibitors
CA2943339A1 (en) 2014-03-21 2015-09-24 Agios Pharmaceuticals, Inc. Compounds and their methods of use
MA49708A (fr) * 2014-04-30 2020-06-03 Pfizer Dérivés de dihétérocycle liés à cycloalkyle
SG11201610333VA (en) 2014-06-13 2017-01-27 Calithera Biosciences Inc Combination therapy with glutaminase inhibitors
WO2016014890A1 (en) 2014-07-24 2016-01-28 Calithera Biosciences, Inc. Treatment of multiple myeloma with heterocyclic inhibitors of glutaminase
US20160287564A1 (en) 2015-03-30 2016-10-06 Calithera Biosciences, Inc. Methods of administering glutaminase inhibitors
JP6944377B2 (ja) 2015-04-06 2021-10-06 キャリセラ バイオサイエンシーズ， インコーポレイテッド グルタミナーゼの阻害剤を用いる肺がんの処置
US10884952B2 (en) 2016-09-30 2021-01-05 Intel Corporation Enforcing memory operand types using protection keys
JP6943759B2 (ja) 2017-12-28 2021-10-06 株式会社東海理化電機製作所 シフト装置

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20140142081A1 (en) * 2012-11-22 2014-05-22 Agios Pharmaceuticals, Inc Compounds and their methods of use

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
Parvin, K. Chin. J. Chem. 2010, 28, 250-254 *

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10125130B2 (en) 2014-04-30 2018-11-13 Pfizer Inc. Cycloalkyl-linked diheterocycle derivatives
US10676471B2 (en) 2014-04-30 2020-06-09 Pfizer Inc. Cycloalkyl-linked diheterocycle derivatives
CN116023375A (zh) * 2021-10-25 2023-04-28 成都苑东生物制药股份有限公司 一种杂环类衍生物、其制备方法及用途

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