WO2020086616A1 - Tyk2 inhibitors and uses thereof - Google Patents

Tyk2 inhibitors and uses thereof Download PDF

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Publication number
WO2020086616A1
WO2020086616A1 PCT/US2019/057485 US2019057485W WO2020086616A1 WO 2020086616 A1 WO2020086616 A1 WO 2020086616A1 US 2019057485 W US2019057485 W US 2019057485W WO 2020086616 A1 WO2020086616 A1 WO 2020086616A1
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Prior art keywords
alkyl
haloalkyl
heterocycloalkyl
cycloalkyl
heteroaryl
Prior art date
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PCT/US2019/057485
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English (en)
French (fr)
Inventor
Bohan Jin
Qing Dong
Gene Hung
Stephen W. Kaldor
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Fronthera US Pharmaceuticals LLC
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Fronthera US Pharmaceuticals LLC
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Priority to SM20250070T priority Critical patent/SMT202500070T1/it
Priority to FIEP19877015.8T priority patent/FI3870579T3/fi
Priority to LTEPPCT/US2019/057485T priority patent/LT3870579T/lt
Priority to PL19877015.8T priority patent/PL3870579T3/pl
Priority to AU2019364336A priority patent/AU2019364336B2/en
Priority to HRP20250048TT priority patent/HRP20250048T1/hr
Priority to KR1020217015306A priority patent/KR102850357B1/ko
Priority to UAA202102676A priority patent/UA130518C2/uk
Application filed by Fronthera US Pharmaceuticals LLC filed Critical Fronthera US Pharmaceuticals LLC
Priority to EP24203217.5A priority patent/EP4480953B1/en
Priority to SG11202104017VA priority patent/SG11202104017VA/en
Priority to CN201980084885.9A priority patent/CN113490664B/zh
Priority to ES19877015T priority patent/ES3011855T3/es
Priority to CA3117200A priority patent/CA3117200A1/en
Priority to EP24203208.4A priority patent/EP4461734B1/en
Priority to SI201930870T priority patent/SI3870579T1/sl
Priority to MX2021004538A priority patent/MX2021004538A/es
Priority to BR112021007679-4A priority patent/BR112021007679A2/pt
Priority to DK19877015.8T priority patent/DK3870579T3/da
Priority to JP2021523157A priority patent/JP7631193B2/ja
Priority to RS20241445A priority patent/RS66346B1/sr
Priority to EP19877015.8A priority patent/EP3870579B1/en
Publication of WO2020086616A1 publication Critical patent/WO2020086616A1/en
Priority to US16/938,183 priority patent/US11053219B2/en
Priority to IL282487A priority patent/IL282487B1/en
Anticipated expiration legal-status Critical
Priority to US17/243,508 priority patent/US12006306B2/en
Priority to US17/713,646 priority patent/US12060343B2/en
Priority to US17/891,817 priority patent/US11731956B2/en
Priority to US18/335,262 priority patent/US12351572B2/en
Priority to JP2025017826A priority patent/JP2025090577A/ja
Ceased legal-status Critical Current

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    • C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • 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
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    • 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
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    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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    • A61P35/00—Antineoplastic agents
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    • A61P37/00—Drugs for immunological or allergic disorders
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    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
    • C07D213/72—Nitrogen atoms
    • C07D213/74—Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
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    • 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
    • C07D401/02—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 two hetero rings
    • C07D401/04—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 two hetero rings directly linked by a ring-member-to-ring-member bond
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    • C07D401/02—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 two hetero rings
    • C07D401/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
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    • 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
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    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
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    • C07D—HETEROCYCLIC COMPOUNDS
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    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
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    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
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    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
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    • C07D498/04—Ortho-condensed systems

Definitions

  • Described herein are compounds, methods of making such compounds, pharmaceutical compositions and medicaments comprising such compounds, and methods of using such compounds for inhibiting nonreceptor tyrosine-protein kinase 2 (“TYK2”), also known as Tyrosine kinase 2.
  • TYK2 nonreceptor tyrosine-protein kinase 2
  • TYK2 is a non-receptor tyrosine kinase member of the Janus kinase (JAKs) family of protein kinases.
  • the mammalian JAK family consists of four members, TYK2, JAK1, JAK2, and JAK3. JAK proteins, including TYK2, are integral to cytokine signaling.
  • TYK2 associates with the cytoplasmic domain of type I and type II cytokine receptors, as well as interferon types I and III receptors, and is activated by those receptors upon cytokine binding. Cytokines implicated in TYK2 activation include interferons (e.g.
  • IFN-a, IFN-b, IFN-k, IFN-d, IFN-e, IFN-t, IFN-w, and IFN-z also known as limitin
  • interleukins e.g. IL-4, IL-6, IL-10, IL-11, IL-12, IL-13, L-22, IL-23, IL-27, IL-31, oncostatin M, ciliary neurotrophic factor, cardiotrophin 1, cardiotrophin-like cytokine, and LIF.
  • the activated TYK2 then goes on to phosphorylate further signaling proteins such as members of the STAT family, including STAT1, STAT2, STAT4, and STAT6.
  • TYK2 activation by IL-23 has been linked to inflammatory bowel disease (IBD), Crohn's disease, and ulcerative colitis.
  • IBD inflammatory bowel disease
  • Crohn's disease Crohn's disease
  • ulcerative colitis A genome-wide association study of 2,622 individuals with psoriasis identified associations between disease susceptibility and TYK2.
  • Knockout or tyrphostin inhibition of TYK2 significantly reduces both IL-23 and IL-22-induced dermatitis.
  • TYK2 also plays a role in respiratory diseases such as asthma, chronic obstructive pulmonary disease (COPD), lung cancer, and cystic fibrosis.
  • COPD chronic obstructive pulmonary disease
  • GCH Goblet cell hyperplasia
  • mucous hypersecretion is mediated by IL-13-induced activation of TYK2, which in turn activates STAT6.
  • TYK2 activity leads to protection of joints from collagen antibody-induced arthritis, a model of human rheumatoid arthritis.
  • decreased Tyk2 activity reduced the production of Th1/Th17-related cytokines and matrix metalloproteases, and other key markers of inflammation.
  • EAE encephalomyelitis
  • MS multiple sclerosis
  • TYK2 is the sole signaling messenger common to both IL-12 and IL-23.
  • TYK2 knockout reduced methylated BSA injection-induced footpad thickness, imiquimod-induced psoriasis-like skin inflammation, and dextran sulfate sodium or 2,4,6-trinitrobenzene sulfonic acid-induced colitis in mice.
  • TYK2 has been shown to play an important role in maintaining tumor surveillance and TYK2 knockout mice showed compromised cytotoxic T cell response, and accelerated tumor development. However, these effects were linked to the efficient suppression of natural killer (NK) and cytotoxic T lymphocytes, suggesting that TYK2 inhibitors would be highly suitable for the treatment of autoimmune disorders or transplant rejection. Although other JAK family members such as JAK3 have similar roles in the immune system, TYK2 has been suggested as a superior target because of its involvement in fewer and more closely related signaling pathways, leading to fewer off-target effects.
  • T-ALL T-cell acute lymphoblastic leukemia
  • TYK2 T-cell acute lymphoblastic leukemia
  • STAT1 STAT1 -mediated signal transduction to maintain cancer cell survival through upregulation of anti-apoptotic protein BCL2.
  • Specific activating mutations to TYK2 that promote cancer cell survival include those to the FERM domain (G36D, S47N, and R425H), the JH2 domain (V73 II), and the kinase domain (E957D and R1027H).
  • TYK2 kinase function of TYK2 is required for increased cancer cell survival, as TYK2 enzymes featuring kinase-dead mutations (M978Y or M978F) in addition to an activating mutation (E957D) resulted in failure to transform.
  • TYK2 has been suggested as a suitable target for patients with IL- 10 and/or BCL2 -addicted tumors, such as 70% of adult T-cell leukemia cases.
  • TYK2 mediated STAT3 signaling has also been shown to mediate neuronal cell death caused by amyloid-b (Ab) peptide.
  • compounds that inhibit the activity of TYK2 are beneficial, especially those with selectivity over JAK2.
  • Such compounds should deliver a pharmacological response that favorably treats one or more of the conditions described herein without the side-effects associated with the inhibition of JAK2.
  • Ring B is cycloalkyl, heterocycloalkyl, aryl, heteroaryl;
  • R 1 and R 2 are independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R 3 is hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl;
  • R 3 and R 4 are taken together to form an optionally substituted ring
  • Ring A is cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; each optionally substituted with one or more R A ;
  • each X is independently -CR x - or -N-;
  • each R 8 is independently hydrogen, CN, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R 9 and R 10 are independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R 11 is C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl, C 1 -C 6 hydroxyalkyl, C 1 -C 6 aminoalkyl, C 2 - C 6 alkenyl, C 2 -C 6 alkynyl, cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently optionally substituted with one or more R 11a ;
  • each R a is independently C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl, C 1 -C 6 hydroxyalkyl,
  • each R c and R d is independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R c and R d are taken together with the nitrogen atom to which they are attached to form a
  • Ring B is cycloalkyl, heterocycloalkyl, aryl, or heteroaryl;
  • R 3 is hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl;
  • R 3 and R 4 are taken together to form an optionally substituted ring
  • Ring A is cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; each optionally substituted with one or more R A ;
  • each X is independently -CR x - or -N-;
  • each R 8 is independently hydrogen, CN, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R 9 and R 10 are independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R 9 and R 10 are taken together with the nitrogen atom to which they are attached to form a
  • each R a is independently C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl, C 1 -C 6 hydroxyalkyl,
  • each R c and R d is independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R c and R d are taken together with the nitrogen atom to which they are attached to form a
  • composition comprising a therapeutically effective amount of the compound disclosed herein, or a pharmaceutically acceptable salt, stereoisomer, or solvate thereof, and a pharmaceutically acceptable excipient.
  • Also disclosed herein is a method of inhibiting a TYK2 enzyme in a patient or biological sample comprising contacting said patient or biological sample with a compound disclosed herein, or a pharmaceutically acceptable salt, stereoisomer, or solvate thereof.
  • a method of treating a TYK2-mediated disorder comprising administering to a patient in need thereof a compound disclosed herein, or a pharmaceutically acceptable salt, stereoisomer, or solvate thereof.
  • the TYK2-mediated disorder is an autoimmune disorder, an inflammatory disorder, a proliferative disorder, an endocrine disorder, a neurological disorder, or a disorder associated with transplantation.
  • the disorder is associated with type I interferon, IL-10, IL-12, or IL-23 signaling.
  • “Aliphatic chain” refers to a linear chemical moiety that is composed of only carbons and hydrogens.
  • the aliphatic chain is saturated.
  • the aliphatic chain is unsaturated.
  • the unsaturated aliphatic chain contains one unsaturation.
  • the unsaturated aliphatic chain contains more than one unsaturation.
  • the unsaturated aliphatic chain contains two unsaturations.
  • the unsaturated aliphatic chain contains one double bond. In some embodiments, the unsaturated aliphatic chain contains two double bonds.
  • Alkyl refers to an optionally substituted straight-chain, or optionally substituted branched- chain saturated hydrocarbon monoradical having from one to about ten carbon atoms, or from one to six carbon atoms. Examples include, but are not limited to, methyl, ethyl, n-propyl, isopropyl, 2-methyl-1- propyl, 2-methyl-2-propyl, 2-methyl-1-butyl, 3-methyl-1-butyl, 2-methyl-3-butyl, 2,2-dimethyl-1-propyl, 2-methyl-1-pentyl, 3-methyl-1-pentyl, 4-methyl-1-pentyl, 2-methyl-2-pentyl, 3-methyl-2-pentyl, 4- methyl-2-pentyl, 2,2-dimethyl-1-butyl, 3,3-dimethyl-1-butyl, 2-ethyl-1-butyl, n-butyl, isobutyl, sec-butyl, t-buty
  • a numerical range such as“C 1 -C 6 alkyl” means that the alkyl group consists of 1 carbon atom, 2 carbon atoms, 3 carbon atoms, 4 carbon atoms, 5 carbon atoms or 6 carbon atoms, although the present definition also covers the occurrence of the term“alkyl” where no numerical range is designated.
  • the alkyl is a C 1 -C 10 alkyl, a C 1 -C 9 alkyl, a C 1 -C 8 alkyl, a C 1 -C 7 alkyl, a C 1 -C 6 alkyl, a C 1 -C 5 alkyl, a C 1 -C 4 alkyl, a C 1 -C 3 alkyl, a C 1 -C 2 alkyl, or a C 1 alkyl.
  • an alkyl group is optionally substituted, for example, with oxo, halogen, amino, nitrile, nitro, hydroxyl, haloalkyl, alkoxy, aryl, cycloalkyl, heterocycloalkyl, heteroaryl, and the like.
  • the alkyl is optionally substituted with oxo, halogen, -CN, -CF 3 , -OH, -OMe, -NH 2 , or -NO 2 .
  • the alkyl is optionally substituted with oxo, halogen, -CN, -CF 3 , -OH, or -OMe.
  • the alkyl is optionally substituted with halogen.
  • Alkenyl refers to an optionally substituted straight-chain, or optionally substituted branched- chain hydrocarbon monoradical having one or more carbon-carbon double-bonds and having from two to about ten carbon atoms, more preferably two to about six carbon atoms.
  • a numerical range such as“C 2 -C 6 alkenyl” means that the alkenyl group may consist of 2 carbon atoms, 3 carbon atoms, 4 carbon atoms, 5 carbon atoms or 6 carbon atoms, although the present definition also covers the occurrence of the term“alkenyl” where no numerical range is designated.
  • the alkenyl is a C 2 -C 10 alkenyl, a C 2 -C 9 alkenyl, a C 2 -C 8 alkenyl, a C 2 -C 7 alkenyl, a C 2 -C 6 alkenyl, a C 2 -C 5 alkenyl, a C 2 -C 4 alkenyl, a C 2 -C 3 alkenyl, or a C 2 alkenyl.
  • an alkenyl group is optionally substituted, for example, with oxo, halogen, amino, nitrile, nitro, hydroxyl, haloalkyl, alkoxy, aryl, cycloalkyl, heterocycloalkyl, heteroaryl, and the like.
  • an alkenyl is optionally substituted with oxo, halogen, -CN, -CF 3 , -OH, -OMe, -NH 2 , or -NO 2 .
  • an alkenyl is optionally substituted with oxo, halogen, -CN, -CF 3 , -OH, or -OMe.
  • the alkenyl is optionally substituted with halogen.
  • Alkynyl refers to an optionally substituted straight-chain or optionally substituted branched- chain hydrocarbon monoradical having one or more carbon-carbon triple-bonds and having from two to about ten carbon atoms, more preferably from two to about six carbon atoms. Examples include, but are not limited to, ethynyl, 2-propynyl, 2-butynyl, 1,3-butadiynyl and the like.
  • a numerical range such as“C 2 -C 6 alkynyl” means that the alkynyl group may consist of 2 carbon atoms, 3 carbon atoms, 4 carbon atoms, 5 carbon atoms or 6 carbon atoms, although the present definition also covers the occurrence of the term“alkynyl” where no numerical range is designated.
  • the alkynyl is a C 2 -C 10 alkynyl, a C 2 -C 9 alkynyl, a C 2 -C 8 alkynyl, a C 2 -C 7 alkynyl, a C 2 -C 6 alkynyl, a C 2 -C 5 alkynyl, a C 2 -C 4 alkynyl, a C 2 -C 3 alkynyl, or a C 2 alkynyl.
  • an alkynyl group is optionally substituted, for example, with oxo, halogen, amino, nitrile, nitro, hydroxyl, haloalkyl, alkoxy, aryl, cycloalkyl, heterocycloalkyl, heteroaryl, and the like.
  • an alkynyl is optionally substituted with oxo, halogen, -CN, - CF 3 , -OH, -OMe, -NH 2 , or -NO 2 .
  • an alkynyl is optionally substituted with oxo, halogen, -CN, -CF 3 , -OH, or -OMe.
  • the alkynyl is optionally substituted with halogen.
  • Alkylene refers to a straight or branched divalent hydrocarbon chain. Unless stated otherwise specifically in the specification, an alkylene group may be optionally substituted, for example, with oxo, halogen, amino, nitrile, nitro, hydroxyl, haloalkyl, alkoxy, aryl, cycloalkyl, heterocycloalkyl, heteroaryl, and the like. In some embodiments, an alkylene is optionally substituted with oxo, halogen, - CN, -CF 3 , -OH, -OMe, -NH 2 , or -NO 2 . In some embodiments, an alkylene is optionally substituted with oxo, halogen, -CN, -CF 3 , -OH, or -OMe. In some embodiments, the alkylene is optionally substituted with halogen.
  • Alkoxy refers to a radical of the formula -OR a where R a is an alkyl radical as defined.
  • an alkoxy group may be optionally substituted, for example, with oxo, halogen, amino, nitrile, nitro, hydroxyl, haloalkyl, alkoxy, aryl, cycloalkyl, heterocycloalkyl, heteroaryl, and the like.
  • an alkoxy is optionally substituted with oxo, halogen, -CN, -CF 3 , -OH, -OMe, -NH 2 , or -NO 2 .
  • an alkoxy is optionally substituted with oxo, halogen, -CN, -CF 3 , -OH, or -OMe.
  • the alkoxy is optionally substituted with halogen.
  • Aminoalkyl refers to an alkyl radical, as defined above, that is substituted by one or more amines. In some embodiments, the alkyl is substituted with one amine. In some embodiments, the alkyl is substituted with one, two, or three amines. Hydroxyalkyl include, for example, aminomethyl, aminoethyl, aminopropyl, aminobutyl, or aminopentyl. In some embodiments, the hydroxyalkyl is aminomethyl.
  • Aryl refers to a radical derived from a hydrocarbon ring system comprising hydrogen, 6 to 30 carbon atoms and at least one aromatic ring.
  • the aryl radical may be a monocyclic, bicyclic, tricyclic or tetracyclic ring system, which may include fused (when fused with a cycloalkyl or heterocycloalkyl ring, the aryl is bonded through an aromatic ring atom) or bridged ring systems.
  • the aryl is a 6- to 10-membered aryl.
  • the aryl is a 6-membered aryl.
  • Aryl radicals include, but are not limited to, aryl radicals derived from the hydrocarbon ring systems of anthrylene, naphthylene, phenanthrylene, anthracene, azulene, benzene, chrysene, fluoranthene, fluorene, as- indacene, s-indacene, indane, indene, naphthalene, phenalene, phenanthrene, pleiadene, pyrene, and triphenylene.
  • the aryl is phenyl.
  • an aryl may be optionally substituted, for example, with halogen, amino, nitrile, nitro, hydroxyl, alkyl, alkenyl, alkynyl, haloalkyl, alkoxy, aryl, cycloalkyl, heterocycloalkyl, heteroaryl, and the like.
  • an aryl is optionally substituted with halogen, methyl, ethyl, -CN, - CF 3 , -OH, -OMe, -NH 2 , or -NO 2 .
  • an aryl is optionally substituted with halogen, methyl, ethyl, -CN, -CF 3 , -OH, or -OMe. In some embodiments, the aryl is optionally substituted with halogen.
  • Cycloalkyl refers to a stable, partially or fully saturated, monocyclic or polycyclic carbocyclic ring, which may include fused (when fused with an aryl or a heteroaryl ring, the cycloalkyl is bonded through a non-aromatic ring atom) or bridged ring systems.
  • Representative cycloalkyls include, but are not limited to, cycloalkyls having from three to fifteen carbon atoms (C 3 -C 15 cycloalkyl), from three to ten carbon atoms (C 3 -C 10 cycloalkyl), from three to eight carbon atoms (C 3 -C 8 cycloalkyl), from three to six carbon atoms (C 3 -C 6 cycloalkyl), from three to five carbon atoms (C 3 -C 5 cycloalkyl), or three to four carbon atoms (C 3 -C 4 cycloalkyl).
  • the cycloalkyl is a 3- to 6-membered cycloalkyl.
  • the cycloalkyl is a 5- to 6-membered cycloalkyl.
  • Monocyclic cycloalkyls include, for example, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, and cyclooctyl.
  • Polycyclic cycloalkyls or carbocycles include, for example, adamantyl, norbornyl, decalinyl, bicyclo[3.3.0]octane, bicyclo[4.3.0]nonane, cis-decalin, trans-decalin, bicyclo[2.1.1]hexane, bicyclo[2.2.1]heptane, bicyclo[2.2.2]octane, bicyclo[3.2.2]nonane, and bicyclo[3.3.2]decane, and 7,7-dimethyl-bicyclo[2.2.1]heptanyl.
  • Partially saturated cycloalkyls include, for example cyclopentenyl, cyclohexenyl, cycloheptenyl, and cyclooctenyl.
  • a cycloalkyl is optionally substituted, for example, with oxo, halogen, amino, nitrile, nitro, hydroxyl, alkyl, alkenyl, alkynyl, haloalkyl, alkoxy, aryl, cycloalkyl, heterocycloalkyl, heteroaryl, and the like.
  • a cycloalkyl is optionally substituted with oxo, halogen, methyl, ethyl, -CN, - CF 3 , -OH, -OMe, -NH 2 , or -NO 2 .
  • a cycloalkyl is optionally substituted with oxo, halogen, methyl, ethyl, -CN, -CF 3 , -OH, or -OMe.
  • the cycloalkyl is optionally substituted with halogen.
  • Deuteroalkyl refers to an alkyl radical, as defined above, that is substituted by one or more deuterium atoms. In some embodiments, the alkyl is substituted with one deuterium atom. In some embodiments, the alkyl is substituted with one, two, or three deuterium atoms. In some embodiments, the alkyl is substituted with one, two, three, four, five, or six deuterium atomss. Deuteroalkyl includes, for example, CD 3 , CH 2 D, CHD 2 , CH 2 CD 3 , CD 2 CD 3 , CHDCD 3 , CH 2 CH 2 D, or CH 2 CHD 2 . In some embodiments, the deuteroalkyl is CD 3 .
  • Haloalkyl refers to an alkyl radical, as defined above, that is substituted by one or more halogen atoms. In some embodiments, the alkyl is substituted with one, two, or three halogen atoms. In some embodiments, the alkyl is substituted with one, two, three, four, five, or six halogen halogens.
  • Haloalkyl includes, for example, trifluoromethyl, difluoromethyl, fluoromethyl, trichloromethyl, 2,2,2-trifluoroethyl, 1,2-difluoroethyl, 3-bromo-2-fluoropropyl, 1,2-dibromoethyl, and the like. In some embodiments, the haloalkyl is trifluoromethyl.
  • Halo or“halogen” refers to bromo, chloro, fluoro or iodo. In some embodiments, halogen is fluoro or chloro. In some embodiments, halogen is fluoro.
  • Heteroalkyl refers to an alkyl group in which one or more skeletal atoms of the alkyl are selected from an atom other than carbon, e.g., oxygen, nitrogen (e.g., -NH-, -N(alkyl)-), sulfur, or combinations thereof.
  • a heteroalkyl is attached to the rest of the molecule at a carbon atom of the heteroalkyl.
  • a heteroalkyl is a C 1 -C 6 heteroalkyl wherein the heteroalkyl is comprised of 1 to 6 carbon atoms and one or more atoms other than carbon, e.g., oxygen, nitrogen (e.g.
  • heteroalkyl is attached to the rest of the molecule at a carbon atom of the heteroalkyl.
  • heteroalkyl examples include, for example, -CH 2 OCH 3 , - CH 2 CH 2 OCH 3 , -CH 2 CH 2 OCH 2 CH 2 OCH 3 , or -CH(CH 3 )OCH 3 .
  • a heteroalkyl is optionally substituted for example, with oxo, halogen, amino, nitrile, nitro, hydroxyl, alkyl, alkenyl, alkynyl, haloalkyl, alkoxy, aryl, cycloalkyl, heterocycloalkyl, heteroaryl, and the like.
  • a heteroalkyl is optionally substituted with oxo, halogen, methyl, ethyl, - CN, -CF 3 , -OH, -OMe, -NH 2 , or -NO 2 .
  • a heteroalkyl is optionally substituted with oxo, halogen, methyl, ethyl, -CN, -CF 3 , -OH, or -OMe. In some embodiments, the heteroalkyl is optionally substituted with halogen.
  • Hydroalkyl refers to an alkyl radical, as defined above, that is substituted by one or more hydroxyls. In some embodiments, the alkyl is substituted with one hydroxyl. In some embodiments, the alkyl is substituted with one, two, or three hydroxyls. Hydroxyalkyl include, for example,
  • hydroxymethyl hydroxyethyl, hydroxypropyl, hydroxybutyl, or hydroxypentyl.
  • the hydroxyalkyl is hydroxymethyl.
  • Heterocycloalkyl refers to a stable 3- to 24-membered partially or fully saturated ring radical comprising 2 to 23 carbon atoms and from one to 8 heteroatoms selected from the group consisting of nitrogen, oxygen, phosphorous and sulfur. In some embodiments, the heterocycloalkyl comprises 1 or 2 heteroatoms selected from nitrogen and oxygen.
  • the heterocycloalkyl radical may be a monocyclic, bicyclic, tricyclic or tetracyclic ring system, which may include fused (when fused with an aryl or a heteroaryl ring, the heterocycloalkyl is bonded through a non-aromatic ring atom) or bridged ring systems; and the nitrogen, carbon or sulfur atoms in the heterocycloalkyl radical may be optionally oxidized; the nitrogen atom may be optionally quaternized.
  • heterocycloalkyls include, but are not limited to, heterocycloalkyls having from two to fifteen carbon atoms (C 2 -C 15 heterocycloalkyl), from two to ten carbon atoms (C 2 -C 10 heterocycloalkyl), from two to eight carbon atoms (C 2 -C 8 heterocycloalkyl), from two to six carbon atoms (C 2 -C 6 heterocycloalkyl), from two to five carbon atoms (C 2 -C 5 heterocycloalkyl), or two to four carbon atoms (C 2 -C 4 heterocycloalkyl).
  • the heterocycloalkyl is a 3- to 6-membered heterocycloalkyl.
  • the cycloalkyl is a 5- to 6-membered heterocycloalkyl.
  • heterocycloalkyl radicals include, but are not limited to, aziridinyl, azetidinyl, dioxolanyl, thienyl[1,3]dithianyl, decahydroisoquinolyl, imidazolinyl, imidazolidinyl, isothiazolidinyl, isoxazolidinyl, morpholinyl, octahydroindolyl, octahydroisoindolyl, 2-oxopiperazinyl, 2-oxopiperidinyl, 2-oxopyrrolidinyl, oxazolidinyl, piperidinyl, piperazinyl, 4-piperidonyl, pyrrolidinyl, pyrazolidinyl, quinuclidinyl, thiazolidinyl, tetrahydrofuryl, trithianyl, tetrahydropyranyl, thiomorpholiny
  • heterocycloalkyl also includes all ring forms of the carbohydrates, including but not limited to, the monosaccharides, the disaccharides and the oligosaccharides.
  • a heterocycloalkyl is optionally substituted, for example, with oxo, halogen, amino, nitrile, nitro, hydroxyl, alkyl, alkenyl, alkynyl, haloalkyl, alkoxy, aryl, cycloalkyl, heterocycloalkyl, heteroaryl, and the like.
  • a heterocycloalkyl is optionally substituted with oxo, halogen, methyl, ethyl, -CN, - CF 3 , -OH, -OMe, -NH 2 , or -NO 2 .
  • a heterocycloalkyl is optionally substituted with oxo, halogen, methyl, ethyl, -CN, -CF 3 , -OH, or -OMe.
  • the heterocycloalkyl is optionally substituted with halogen.
  • Heteroalkyl refers to an alkyl group in which one or more skeletal atoms of the alkyl are selected from an atom other than carbon, e.g., oxygen, nitrogen (e.g. -NH-, -N(alkyl)-), sulfur, or combinations thereof.
  • a heteroalkyl is attached to the rest of the molecule at a carbon atom of the heteroalkyl.
  • a heteroalkyl is a C 1 -C 6 heteroalkyl.
  • a Heteroalkyl is optionally substituted, for example, with oxo, halogen, amino, nitrile, nitro, hydroxyl, alkyl, alkenyl, alkynyl, haloalkyl, alkoxy, aryl, cycloalkyl, heterocycloalkyl, heteroaryl, and the like.
  • a heteroalkyl is optionally substituted with oxo, halogen, methyl, ethyl, -CN, -CF 3 , -OH, -OMe, -NH 2 , or -NO 2 .
  • a heteroalkyl is optionally substituted with oxo, halogen, methyl, ethyl, -CN, -CF 3 , -OH, or -OMe. In some embodiments, the heteroalkyl is optionally substituted with halogen.
  • Heteroaryl refers to a 5- to 14-membered ring system radical comprising hydrogen atoms, one to thirteen carbon atoms, one to six heteroatoms selected from the group consisting of nitrogen, oxygen, phosphorous and sulfur, and at least one aromatic ring.
  • the heteroaryl radical may be a monocyclic, bicyclic, tricyclic or tetracyclic ring system, which may include fused (when fused with a cycloalkyl or heterocycloalkyl ring, the heteroaryl is bonded through an aromatic ring atom) or bridged ring systems; and the nitrogen, carbon or sulfur atoms in the heteroaryl radical may be optionally oxidized; the nitrogen atom may be optionally quaternized.
  • the heteroaryl is a 5- to 10-membered heteroaryl. In some embodiments, the heteroaryl is a 5- to 6-membered heteroaryl. Examples include, but are not limited to, azepinyl, acridinyl, benzimidazolyl, benzothiazolyl, benzindolyl, benzodioxolyl, benzofuranyl, benzooxazolyl, benzothiazolyl, benzothiadiazolyl, benzo[b][1,4]dioxepinyl, 1,4-benzodioxanyl, benzonaphthofuranyl, benzoxazolyl, benzodioxolyl, benzodioxinyl, benzopyranyl, benzopyranonyl, benzofuranyl, benzofuranonyl, benzothienyl
  • a heteroaryl is optionally substituted, for example, with halogen, amino, nitrile, nitro, hydroxyl, alkyl, alkenyl, alkynyl, haloalkyl, alkoxy, aryl, cycloalkyl, heterocycloalkyl, heteroaryl, and the like.
  • a heteroaryl is optionally substituted with halogen, methyl, ethyl, -CN, - CF 3 , -OH, -OMe, -NH 2 , or -NO 2 .
  • a heteroaryl is optionally substituted with halogen, methyl, ethyl, -CN, -CF 3 , -OH, or -OMe.
  • the heteroaryl is optionally substituted with halogen.
  • the disclosed methods can provide any amount of any level of treatment, prevention, amelioration, or inhibition of the disorder in a mammal.
  • a disorder, including symptoms or conditions thereof may be reduced by, for example, about 100%, about 90%, about 80%, about 70%, about 60%, about 50%, about 40%, about 30%, about 20%, or about 10%.
  • the treatment, prevention, amelioration, or inhibition provided by the methods disclosed herein can include treatment, prevention, amelioration, or inhibition of one or more conditions or symptoms of the disorder, e.g., cancer or an inflammatory disease.
  • “treatment,”“prevention,” “amelioration,” or“inhibition” encompass delaying the onset of the disorder, or a symptom or condition thereof.
  • an“effective amount” or“therapeutically effective amount,” as used herein, refer to a sufficient amount of a compound disclosed herein being administered which will relieve to some extent one or more of the symptoms of the disease or condition being treated, e.g., cancer or an inflammatory disease. In some embodiments, the result is a reduction and/or alleviation of the signs, symptoms, or causes of a disease, or any other desired alteration of a biological system.
  • an“effective amount” for therapeutic uses is the amount of the composition comprising a compound disclosed herein required to provide a clinically significant decrease in disease symptoms.
  • an appropriate“effective” amount in any individual case is determined using techniques, such as a dose escalation study.
  • TYK2 -mediated disorders, diseases, and/or conditions means any disease or other deleterious condition in which TYK2 or a mutant thereof is known to play a role. Accordingly, another embodiment relates to treating or lessening the severity of one or more diseases in which TYK2, or a mutant thereof, is known to play a role.
  • TYK2-mediated disorders include but are not limited to autoimmune disorders, inflammatory disorders, proliferative disorders, endocrine disorders, neurological disorders and disorders associated with transplantation.
  • the TYK2-mediated disorder is an autoimmune disorder, an inflammatory disorder, a proliferative disorder, an endocrine disorder, a neurological disorder, or a disorder associated with transplantation.
  • each R Z is independently hydrogen, deuterium, halogen, -CN, -OR b , -NR c R d , C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl;
  • R 1 and R 2 are independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R 3 is hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl;
  • R 3 and R 4 are taken together to form an optionally substituted ring
  • Ring A is cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; each optionally substituted with one or more R A ;
  • R 9 and R 10 are independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R 9 and R 10 are taken together with the nitrogen atom to which they are attached to form a
  • each R a is independently C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl, C 1 -C 6 hydroxyalkyl,
  • each R c and R d is independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R c and R d are taken together with the nitrogen atom to which they are attached to form a
  • Ring A is heterocycloalkyl or heteroaryl; each optionally substituted with one or more R A .
  • Ring A is a 5-membered heterocycloalkyl or a 5-membered heteroaryl; each optionally substituted with one or more R A .
  • Ring A is heteroaryl optionally substituted with one or more R A .
  • each R A is independently deuterium, halogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl. In some embodiments of a compound of Formula (I), each R A is independently halogen or C 1 -C 6 alkyl. In some embodiments of a compound of Formula (I), each R A is independently C 1 -C 6 alkyl.
  • R 4 is hydrogen or -OR b .
  • R 4 is -OR b .
  • R 4 is hydrogen.
  • the compound is of Formula (Ia):
  • the compound is of Formula (Ib):
  • R 3 is hydrogen or
  • R 3 is hydrogen.
  • Z is a bond or -CH 2 -. In some embodiments of a compound of Formula (I), (Ia), or (Ib), Z is -CH 2 -. In some embodiments of a compound of Formula (I), (Ia), or (Ib), Z is a bond.
  • R 1 and R 2 are independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl. In some embodiments of a compound of Formula (I), (Ia), or (Ib), R 1 and R 2 are independently hydrogen or C 1 -C 6 deuteroalkyl. In some embodiments of a compound of Formula (I), (Ia), or (Ib), R 1 is hydrogen. In some embodiments of a compound of Formula (I), (Ia), or (Ib), R 2 is C 1 -C 6 alkyl or C 1 -C 6 deuteroalkyl. In some embodiments of a compound of Formula (I), (Ia), or (Ib), R 2 is C 1 -C 6 deuteroalkyl.
  • R 7 is C 1 -C 6 alkyl
  • R 7 is unsubstituted cycloalkyl.
  • R 1 and R 2 are independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R 3 is hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl;
  • R 3 and R 4 are taken together to form an optionally substituted ring
  • Ring A is cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; each optionally substituted with one or more R A ;
  • X is -CR x - or -N-;
  • R x and R 5 are taken together to form ring D optionally substituted with one or more R D ;
  • Ring D is a cycloalkyl, heterocycloalkyl, aryl, or heteroaryl;
  • R 9 and R 10 are independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R 9 and R 10 are taken together with the nitrogen atom to which they are attached to form a
  • each R a is independently C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl, C 1 -C 6 hydroxyalkyl,
  • each R c and R d is independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R c and R d are taken together with the nitrogen atom to which they are attached to form a
  • Ring A is heterocycloalkyl or heteroaryl; each optionally substituted with one or more R A .
  • Ring A is a 5-membered heterocycloalkyl or a 5-membered heteroaryl; each optionally substituted with one or more R A .
  • Ring A is heteroaryl optionally substituted with one or more R A .
  • each R A is independently deuterium, halogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl. In some embodiments of a compound of Formula (II) or (II’), each R A is independently halogen or C 1 -C 6 alkyl. In some embodiments of a compound of Formula (II) or (II’), each R A is independently C 1 -C 6 alkyl.
  • R 4 is hydrogen or -OR b .
  • R 4 is -OR b .
  • R 4 is hydrogen.
  • X is -CH-. In some embodiments of a compound of Formula (II) or (II’), X is -N-.
  • the compound is of Formula (IIa) or (II’a):
  • the compound is of Formula (IIb) or (II’b):
  • R 3 is hydrogen or C 1 -C 6 alkyl. In some embodiments of a compound of Formula (II), (II’), (IIa), (II’a), (IIb), or (II’b), R 3 is hydrogen.
  • R 1 and R 2 are independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl.
  • R 1 and R 2 are independently hydrogen or C 1 -C 6 deuteroalkyl.
  • R 1 is hydrogen.
  • R 2 is C 1 -C 6 alkyl or C 1 -C 6 deuteroalkyl.
  • R 2 is C 1 -C 6 deuteroalkyl.
  • R 7 is unsubstituted cycloalkyl.
  • R 9 and R 10 are independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl, cycloalkyl,
  • R 11 is deuterium, halogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl.
  • R 11 is halogen.
  • R 11 is hydrogen.
  • Ring B is a cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; provided that is not
  • n 0-4;
  • each Y is independently C or N;
  • R 3 is hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl;
  • R 3 and R 4 are taken together to form an optionally substituted ring
  • Ring A is cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; each optionally substituted with one or more R A ;
  • X is -CR x - or -N-;
  • R x and R 5 are taken together to form ring D optionally substituted with one or more R D ;
  • Ring D is a cycloalkyl, heterocycloalkyl, aryl, or heteroaryl;
  • R 9 and R 10 are taken together with the nitrogen atom to which they are attached to form a
  • each R a is independently C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl, C 1 -C 6 hydroxyalkyl,
  • each R c and R d is independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R c and R d are taken together with the nitrogen atom to which they are attached to form a
  • Ring A is heterocycloalkyl or heteroaryl; each optionally substituted with one or more R A .
  • Ring A is a 5-membered heterocycloalkyl or a 5-membered heteroaryl; each optionally substituted with one or more R A .
  • Ring A is heteroaryl optionally substituted with one or more R A .
  • each R A is independently deuterium, halogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl. In some embodiments of a compound of Formula (III), each R A is independently halogen or C 1 -C 6 alkyl. In some embodiments of a compound of Formula (III), each R A is independently C 1 -C 6 alkyl.
  • R 4 is hydrogen or -OR b .
  • R 4 is -OR b .
  • R 4 is hydrogen.
  • X is -CH-. In some embodiments of a compound of Formula (III), X is -N-.
  • the compound is of Formula (IIIa):
  • the compound is of Formula (IIIb):
  • R 3 is hydrogen or C 1 -C 6 alkyl. In some embodiments of a compound of Formula (III), (IIIa), or (IIIb), R 3 is hydrogen.
  • R 7 is C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl, aryl, or heteroaryl; wherein each alkyl, cycloalkyl, heterocycloal
  • R 7 is unsubstituted cycloalkyl.
  • Ring B is a heterocycloalkyl or heteroaryl.
  • each R B is independently hydrogen, deuterium, halogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl; two R B on the same carbon are taken together to form an oxo.
  • n is 0. In some embodiments of a compound of Formula (III), (IIIa), or (IIIb), n is 1. In some embodiments of a compound of Formula (III), (IIIa), or (IIIb), n is 2. In some embodiments of a compound of Formula (III), (IIIa), or (IIIb), n is 0-2. In some embodiments of a compound of Formula (III), (IIIa), or (IIIb), n is 0 or 1. In some embodiments of a compound of Formula (III), (IIIa), or (IIIb), n is 1 or 2. In some embodiments of a compound of Formula (III), (IIIa), or (IIIb), n is 1-3.
  • n’ is 0. In some embodiments of a compound of Formula (III), (IIIa), or (IIIb), n’ is 1. In some embodiments of a compound of Formula (III), (IIIa), or (IIIb), n’ is 2. In some embodiments of a compound of Formula (III), (IIIa), or (IIIb), n’ is 0-2. In some embodiments of a compound of Formula (III), (IIIa), or (IIIb), n’ is 0 or 1. In some embodiments of a compound of Formula (III), (IIIa), or (IIIb), n’ is 1 or 2.
  • Ring C is a bicyclic ring system
  • n 0-4;
  • R 1 and R 2 are independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • L 1 is -O-, -NH-, or -N(CH 3 )-;
  • Ring A is cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; each optionally substituted with one or more R A ;
  • X is -CR x - or -N-;
  • R x and R 5 are taken together to form ring D optionally substituted with one or more R D ;
  • Ring D is a cycloalkyl, heterocycloalkyl, aryl, or heteroaryl;
  • R 9 and R 10 are taken together with the nitrogen atom to which they are attached to form a
  • each R a is independently C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl, C 1 -C 6 hydroxyalkyl,
  • each R c and R d is independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R c and R d are taken together with the nitrogen atom to which they are attached to form a
  • Ring A is heterocycloalkyl or heteroaryl; each optionally substituted with one or more R A .
  • Ring A is a 5-membered heterocycloalkyl or a 5-membered heteroaryl; each optionally substituted with one or more R A .
  • Ring A is heteroaryl optionally substituted with one or more R A .
  • each R A is independently deuterium, halogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl. In some embodiments of a compound of Formula (IV), each R A is independently halogen or C 1 -C 6 alkyl. In some embodiments of a compound of Formula (IV), each R A is independently C 1 -C 6 alkyl.
  • R 4 is hydrogen or -OR b .
  • R 4 is -OR b .
  • R 4 is hydrogen.
  • X is -CH-. In some embodiments of a compound of Formula (IV), X is -N-.
  • the compound is of Formula (IVa):
  • the compound is of Formula (IVb):
  • R 1 and R 2 are independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl. In some embodiments of a compound of Formula (IV), (IVa), or (IVb), R 1 and R 2 are independently hydrogen or C 1 -C 6 deuteroalkyl. In some embodiments of a compound of Formula (IV), (IVa), or (IVb), R 1 is hydrogen. In some embodiments of a compound of Formula (IV), (IVa), or (IVb), R 2 is C 1 -C 6 alkyl or C 1 -C 6 deuteroalkyl. In some embodiments of a compound of Formula (IV), (IVa), or (IVb), R 2 is C 1 -C 6 deuteroalkyl.
  • L 1 is -NH-. In some embodiments of a compound of Formula (IV), (IVa), or (IVb), L 1 is -O- or -NH-.
  • R 13 is C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl.
  • R 7 is C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl, aryl, or heteroaryl; wherein each alkyl, cycloalkyl, heterocycloal
  • R 7 is unsubstituted cycloalkyl.
  • R 9 and R 10 are independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl, cycloalkyl, heterocycloalkyl,
  • Ring C is indole or benzimidazole.
  • each R C is independently deuterium, halogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl. In some embodiments of a compound of Formula (IV), (IVa), or (IVb), each R C is independently halogen or C 1 -C 6 alkyl.
  • m is 0. In some embodiments of a compound of Formula (IV), (IVa), or (IVb), m is 1. In some embodiments of a compound of Formula (IV), (IVa), or (IVb), m is 2. In some embodiments of a compound of Formula (IV), (IVa), or (IVb), m is 0 or 1. In some embodiments of a compound of Formula (IV), (IVa), or (IVb), m is 0-2. In some embodiments of a compound of Formula (IV), (IVa), or (IVb), m is 1 or 2. In some embodiments of a compound of Formula (IV), (IVa), or (IVb), m is 1-3.
  • Ring D is a cycloalkyl, heterocycloalkyl, aryl, or heteroaryl;
  • r 0-4;
  • each Y is independently C or N;
  • R 1 and R 2 are independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R 3 is hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl;
  • R 3 and R 4 are taken together to form an optionally substituted ring
  • Ring A is cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; each optionally substituted with one or more R A ;
  • each X is independently -CR x - or -N-;
  • each R c and R d is independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R c and R d are taken together with the nitrogen atom to which they are attached to form a
  • Ring A is heterocycloalkyl or heteroaryl; each optionally substituted with one or more R A .
  • Ring A is a 5-membered heterocycloalkyl or a 5-membered heteroaryl; each optionally substituted with one or more R A .
  • Ring A is heteroaryl optionally substituted with one or more R A .
  • each R A is independently deuterium, halogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl. In some embodiments of a compound of Formula (V), each R A is independently halogen or C 1 -C 6 alkyl. In some embodiments of a compound of Formula (V), each R A is independently C 1 -C 6 alkyl.
  • R 4 is hydrogen or -OR b .
  • R 4 is -OR b .
  • R 4 is hydrogen.
  • each X is -N-.
  • each X is -CH-.
  • one X is -N- and the other is -CH-.
  • the compound is of Formula (Va):
  • the compound is of Formula (Vb):
  • R 3 is hydrogen or C 1 -C 6 alkyl. In some embodiments of a compound of Formula (V), (Va), or (Vb), R 3 is hydrogen.
  • R 1 and R 2 are independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl. In some embodiments of a compound of Formula (V), (Va), or (Vb), R 1 and R 2 are independently hydrogen or C 1 -C 6 deuteroalkyl. In some embodiments of a compound of Formula (V), (Va), or (Vb), R 1 is hydrogen. In some embodiments of a compound of Formula (V), (Va), or (Vb), R 2 is C 1 -C 6 alkyl or C 1 -C 6 deuteroalkyl. In some embodiments of a compound of Formula (V), (Va), or (Vb), R 2 is C 1 -C 6 deuteroalkyl.
  • Ring D is a
  • heterocycloalkyl or heteroaryl are heterocycloalkyl or heteroaryl.
  • each R D is independently hydrogen, deuterium, halogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl, or cycloalkyl. In some embodiments of a compound of Formula (V), (Va), or (Vb), each R D is independently hydrogen or cycloalkyl.
  • r is 0. In some embodiments of a compound of Formula (V), (Va), or (Vb), r is 1. In some embodiments of a compound of Formula (V), (Va), or (Vb), r is 2. In some embodiments of a compound of Formula (V), (Va), or (Vb), r is 0-2. In some embodiments of a compound of Formula (V), (Va), or (Vb), r is 0 or 1. In some embodiments of a compound of Formula (V), (Va), or (Vb), r is 1 or 2. In some embodiments of a compound of Formula (V), (Va), or (Vb), r is 1-3.
  • r’ is 0. In some embodiments of a compound of Formula (V), (Va), or (Vb), r’ is 1. In some embodiments of a compound of Formula (V), (Va), or (Vb), r’ is 2. In some embodiments of a compound of Formula (V), (Va), or (Vb), r’ is 0-2. In some embodiments of a compound of Formula (V), (Va), or (Vb), r’ is 0 or 1. In some embodiments of a compound of Formula (V), (Va), or (Vb), r’ is 1 or 2. In some embodiments of a compound of Formula (V), (Va), or (Vb), r’ is 1-3.
  • Ring E is cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; each optionally substituted with one or more R E ;
  • L 2 is a bond, -O-, or
  • R 1 and R 2 are independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R 3 is hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl;
  • R 3 and R 4 are taken together to form an optionally substituted ring
  • Ring A is cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; each optionally substituted with one or more R A ;
  • X is -CR x - or -N-;
  • each R a is independently C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl, C 1 -C 6 hydroxyalkyl,
  • each R c and R d is independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R c and R d are taken together with the nitrogen atom to which they are attached to form a
  • Ring A is heterocycloalkyl or heteroaryl; each optionally substituted with one or more R A .
  • Ring A is a 5-membered heterocycloalkyl or a 5-membered heteroaryl; each optionally substituted with one or more R A .
  • Ring A is heteroaryl optionally substituted with one or more R A .
  • each R A is independently deuterium, halogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl. In some embodiments of a compound of Formula (VI), each R A is independently halogen or C 1 -C 6 alkyl. In some embodiments of a compound of Formula (VI), each R A is independently C 1 -C 6 alkyl.
  • R 4 is hydrogen or -OR b .
  • R 4 is -OR b .
  • R 4 is hydrogen.
  • X is -CH-. In some embodiments of a compound of Formula (VI), X is -N-.
  • the compound is of Formula (VIa):
  • the compound is of Formula (VIb):
  • R 3 is hydrogen or C 1 -C 6 alkyl. In some embodiments of a compound of Formula (VI), (VIa), or (VIb), R 3 is hydrogen.
  • R 1 and R 2 are independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl. In some embodiments of a compound of Formula (VI), (VIa), or (VIb), R 1 and R 2 are independently hydrogen or C 1 -C 6 deuteroalkyl. In some embodiments of a compound of Formula (VI), (VIa), or (VIb), R 1 is hydrogen. In some embodiments of a compound of Formula (VI), (VIa), or (VIb), R 2 is C 1 -C 6 alkyl or C 1 -C 6 deuteroalkyl. In some embodiments of a compound of Formula (VI), (VIa), or (VIb), R 2 is C 1 -C 6 deuteroalkyl.
  • L 2 is a bond.
  • Ring E is cycloalkyl, heterocycloalkyl, or aryl; each optionally substituted with one or more R E .
  • Ring E is aryl optionally substituted with one or more R E .
  • each R E is independently deuterium, halogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl.
  • each R E is independently halogen.
  • R 3 is hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl;
  • R 3 and R 4 are taken together to form an optionally substituted ring
  • Ring A is cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; each optionally substituted with one or more R A ;
  • X is -CR x - or -N-;
  • each R a is independently C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl, C 1 -C 6 hydroxyalkyl,
  • Ring D is a cycloalkyl, heterocycloalkyl, aryl, or heteroaryl;
  • R 9 and R 10 are independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R 9 and R 10 are taken together with the nitrogen atom to which they are attached to form a
  • each R c and R d is independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • Ring A is heterocycloalkyl or heteroaryl; each optionally substituted with one or more R A .
  • Ring A is a 5-membered heterocycloalkyl or a 5-membered heteroaryl; each optionally substituted with one or more R A .
  • Ring A is heteroaryl optionally substituted with one or more R A .
  • each R A is independently deuterium, halogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl. In some embodiments of a compound of Formula (VII), each R A is independently halogen or C 1 -C 6 alkyl. In some embodiments of a compound of Formula (VII), each R A is independently C 1 -C 6 alkyl.
  • R 4 is hydrogen or -OR b .
  • R 4 is -OR b .
  • R 4 is hydrogen.
  • X is -CH-. In some embodiments of a compound of Formula (VII), X is -N-.
  • the compound is of Formula (VIIb):
  • R 3 is hydrogen or C 1 -C 6 alkyl. In some embodiments of a compound of Formula (VII), (VIIa), or (VIIb), R 3 is hydrogen.
  • R 7 is unsubstituted cycloalkyl.
  • R 9 and R 10 are independently hydrogen,
  • R 14 is hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl, or C 1 -C 6 alkyl(cycloalkyl). In some embodiments of a compound of Formula (VII), (VIIa), or (VIIb), R 14 is C 1 -C 6 alkyl or C 1 -C 6 alkyl(cycloalkyl).
  • L 3 is -O-, -NH-, or -N(CH 3 )-;
  • R 3 is hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl;
  • R 3 and R 4 are taken together to form an optionally substituted ring
  • Ring A is cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; each optionally substituted with one or more R A ;
  • X is -CR x - or -N-;
  • each R a is independently C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl, C 1 -C 6 hydroxyalkyl,
  • R x and R 5 are taken together to form ring D optionally substituted with one or more R D ;
  • Ring D is a cycloalkyl, heterocycloalkyl, aryl, or heteroaryl;
  • R 9 and R 10 are independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R 9 and R 10 are taken together with the nitrogen atom to which they are attached to form a
  • each R c and R d is independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R c and R d are taken together with the nitrogen atom to which they are attached to form a
  • each R A is independently deuterium, halogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl. In some embodiments of a compound of Formula (VIII), each R A is independently halogen or C 1 -C 6 alkyl. In some embodiments of a compound of Formula (VIII), each R A is independently C 1 -C 6 alkyl.
  • R 4 is hydrogen or -OR b .
  • R 4 is -OR b .
  • R 4 is hydrogen.
  • X is -CH-. In some embodiments of a compound of Formula (VIII), X is -N-.
  • R 7 is unsubstituted cycloalkyl.
  • R 9 and R 10 are independently hydrogen,
  • L 3 is -O-. In some embodiments of a compound of Formula (VIII), (VIIIa), or (VIIIb), L 3 is -NH-.
  • R 15 is C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl, or cycloalkyl.
  • L 4 is -NR 3 -.
  • R 3 is hydrogen or C 1 -C 6 alkyl. In some embodiments of a compound of Formula (VIII), (VIIIa), or (VIIIb), R 3 is hydrogen.
  • Ring F is a heterocycloalkyl or heteroaryl
  • R 3 is hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl;
  • R 3 and R 4 are taken together to form an optionally substituted ring
  • Ring A is cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; each optionally substituted with one or more R A ;
  • X is -CR x - or -N-;
  • R x and R 5 are taken together to form ring D optionally substituted with one or more R D ;
  • Ring D is a cycloalkyl, heterocycloalkyl, aryl, or heteroaryl;
  • R 9 and R 10 are independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R 9 and R 10 are taken together with the nitrogen atom to which they are attached to form a
  • each R a is independently C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl, C 1 -C 6 hydroxyalkyl,
  • each R c and R d is independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • Ring A is heterocycloalkyl or heteroaryl; each optionally substituted with one or more R A .
  • Ring A is a 5-membered heterocycloalkyl or a 5-membered heteroaryl; each optionally substituted with one or more R A .
  • Ring A is heteroaryl optionally substituted with one or more R A .
  • each R A is independently deuterium, halogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl. In some embodiments of a compound of Formula (IX), each R A is independently halogen or C 1 -C 6 alkyl. In some embodiments of a compound of Formula (IX), each R A is independently C 1 -C 6 alkyl.
  • R 4 is hydrogen or -OR b .
  • R 4 is -OR b .
  • R 4 is hydrogen.
  • X is -CH-. In some embodiments of a compound of Formula (IX), X is -N-.
  • R 3 is hydrogen or C 1 -C 6 alkyl. In some embodiments of a compound of Formula (IX), (IXa), or (IXb), R 3 is hydrogen.
  • R 7 is C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl, aryl, or heteroaryl; wherein each alkyl, cycloalkyl, heterocycloal
  • R 7 is unsubstituted cycloalkyl.
  • R 9 and R 10 are independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl, aryl, or heteroaryl; wherein each alkyl
  • Ring F is a heterocycloalkyl.
  • each R F is
  • each R F is independently hydrogen, deuterium, halogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl.
  • p is 0. In some embodiments of a compound of Formula (IX), (IXa), or (IXb), p is 0. In some embodiments of a compound of Formula (IX), (IXa), or (IXb), p is 1. In some embodiments of a compound of Formula (IX), (IXa), or (IXb), p is 2. In some embodiments of a compound of Formula (IX), (IXa), or (IXb), p is 0-2. In some embodiments of a compound of Formula (IX), (IXa), or (IXb), p is 0 or 1. In some embodiments of a compound of Formula (IX), (IXa), or (IXb), p is 1 or 2. In some embodiments of a compound of Formula (IX), (IXa), or (IXb), p is 1-3.
  • R 1 and R 2 are independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • L 1 is -O-, -NH-, or -N(CH 3 )-;
  • R 3 is hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl;
  • R 3 and R 4 are taken together to form an optionally substituted ring
  • X is -CR x - or -N-;
  • each R a is independently C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl, C 1 -C 6 hydroxyalkyl,
  • each R c and R d is independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R c and R d are taken together with the nitrogen atom to which they are attached to form a
  • Ring A is heterocycloalkyl or heteroaryl; each optionally substituted with one or more R A .
  • Ring A is a 5-membered heterocycloalkyl or a 5-membered heteroaryl; each optionally substituted with one or more R A .
  • Ring A is heteroaryl optionally substituted with one or more R A .
  • each R A is independently deuterium, halogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl. In some embodiments of a compound of Formula (X), each R A is independently halogen or C 1 -C 6 alkyl. In some embodiments of a compound of Formula (X), each R A is independently C 1 -C 6 alkyl.
  • R 4 is hydrogen or -OR b .
  • R 4 is -OR b .
  • R 4 is hydrogen.
  • X is -CH-. In some embodiments of a compound of Formula (X), X is -N-.
  • the compound is of
  • R 3 is hydrogen or C 1 -C 6 alkyl. In some embodiments of a compound of Formula (X), (Xa), (Xa-1), (Xb), or (Xb-1), R 3 is hydrogen.
  • R 1 and R 2 are independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl. In some embodiments of a compound of Formula (X), (Xa), (Xa-1), (Xb), or (Xb-1), R 1 and R 2 are independently hydrogen or C 1 -C 6 deuteroalkyl. In some embodiments of a compound of Formula (X), (Xa), (Xa-1), (Xb), or (Xb-1), R 1 is hydrogen.
  • R 2 is C 1 -C 6 alkyl or C 1 -C 6 deuteroalkyl. In some embodiments of a compound of Formula (X), (Xa), (Xa-1), (Xb), or (Xb-1), R 2 is C 1 -C 6 deuteroalkyl.
  • R 12 is -L 1 - R 13 .
  • L 1 is - NH-. In some embodiments of a compound of Formula (X), (Xa), (Xa-1), (Xb), or (Xb-1), L 1 is -O- or - NH-.
  • R 13 is C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl.
  • L 5 is a saturated linear aliphatic chain having 1-8 carbon atoms optionally substituted with one or more R L5 , wherein 1, 2, or 3 carbon atoms are optionally replaced with -NH-, -N(CH 3 )-, or -O-.
  • L 5 is a saturated linear aliphatic chain having 1-8 carbon atoms optionally substituted with one or more R L5 , wherein 1, 2, or 3 carbon atoms are optionally replaced with -NH- or -O-.
  • L 5 is a saturated linear aliphatic chain having 1-8 carbon atoms, wherein 1, 2, or 3 carbon atoms are optionally replaced with -NH-, -N(CH 3 )-, or -O-. In some embodiments of a compound of Formula (X), (Xa), (Xa-1), (Xb), or (Xb-1), L 5 is a saturated linear aliphatic chain having 1-8 carbon atoms, wherein 1, 2, or 3 carbon atoms are optionally replaced with - NH- or -O-.
  • L 5 is an unsaturated linear aliphatic chain having 1-8 carbon atoms optionally substituted with one or more R L5 , wherein 1, 2, or 3 carbon atoms are optionally replaced with -NH-, -N(CH 3 )-, or -O-.
  • L 5 is an unsaturated linear aliphatic chain having 1-8 carbon atoms optionally substituted with one or more R L5 , wherein 1, 2, or 3 carbon atoms are optionally replaced with -NH- or -O-.
  • L 5 is an unsaturated linear aliphatic chain having 1-8 carbon atoms, wherein 1, 2, or 3 carbon atoms are optionally replaced with -NH-, -N(CH 3 )-, or -O-. In some embodiments of a compound of Formula (X), (Xa), (Xa-1), (Xb), or (Xb-1), L 5 is an unsaturated linear aliphatic chain having 1-8 carbon atoms, wherein 1, 2, or 3 carbon atoms are optionally replaced with -NH- or -O-.
  • each R L5 is independently deuterium, halogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl. In some embodiments of a compound of Formula (X), (Xa), (Xa-1), (Xb), or (Xb- 1), each R L5 is independently deuterium or halogen.
  • L 5 is .
  • R 3 is hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl;
  • R 3 and R 4 are taken together to form an optionally substituted ring
  • Ring A is cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; each optionally substituted with one or more R A ;
  • X is -CR x - or -N-;
  • R x and R 5 are taken together to form ring D optionally substituted with one or more R D ;
  • Ring D is a cycloalkyl, heterocycloalkyl, aryl, or heteroaryl;
  • R 9 and R 10 are taken together with the nitrogen atom to which they are attached to form a
  • each R a is independently C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl, C 1 -C 6 hydroxyalkyl,
  • each R c and R d is independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R c and R d are taken together with the nitrogen atom to which they are attached to form a
  • Ring A is heterocycloalkyl or heteroaryl; each optionally substituted with one or more R A .
  • Ring A is a 5-membered heterocycloalkyl or a 5-membered heteroaryl; each optionally substituted with one or more R A .
  • Ring A is heteroaryl optionally substituted with one or more R A .
  • each R A is independently deuterium, halogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl. In some embodiments of a compound of Formula (XI), each R A is independently halogen or C 1 -C 6 alkyl. In some embodiments of a compound of Formula (XI), each R A is independently C 1 -C 6 alkyl.
  • R 4 is hydrogen or -OR b .
  • R 4 is -OR b .
  • R 4 is hydrogen.
  • X is -CH-. In some embodiments of a compound of Formula (XI), X is -N-.
  • R 3 is hydrogen or C 1 -C 6 alkyl. In some embodiments of a compound of Formula (XI), (XIa), or (XIb), R 3 is hydrogen.
  • R 7 is C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl, aryl, or heteroaryl; wherein each alkyl, cycloalkyl, heterocycloal
  • R 7 is unsubstituted cycloalkyl.
  • L 6 is a saturated linear aliphatic chain having 1-8 carbon atoms optionally substituted with one or more R L6 , wherein 1, 2, or 3 carbon atoms are optionally replaced with -NH-, -N(CH 3 )-, or -O-.
  • L 6 is a saturated linear aliphatic chain having 1-8 carbon atoms optionally substituted with one or more R L6 , wherein 1, 2, or 3 carbon atoms are optionally replaced with -NH- or -O-.
  • L 6 is a saturated linear aliphatic chain having 1-8 carbon atoms, wherein 1, 2, or 3 carbon atoms are optionally replaced with -NH-, -N(CH 3 )-, or -O-.
  • L 6 is a saturated linear aliphatic chain having 1-8 carbon atoms, wherein 1, 2, or 3 carbon atoms are optionally replaced with -NH- or -O-.
  • L 6 is an unsaturated linear aliphatic chain having 1-8 carbon atoms optionally substituted with one or more R L6 , wherein 1, 2, or 3 carbon atoms are optionally replaced with -NH-, -N(CH 3 )-, or -O-.
  • L 6 is an unsaturated linear aliphatic chain having 1-8 carbon atoms optionally substituted with one or more R L6 , wherein 1, 2, or 3 carbon atoms are optionally replaced with -NH- or -O-.
  • L 6 is an unsaturated linear aliphatic chain having 1-8 carbon atoms, wherein 1, 2, or 3 carbon atoms are optionally replaced with -NH-, -N(CH 3 )-, or -O-. In some embodiments of a compound of Formula (XI), (XIa), or (XIb), L 6 is an unsaturated linear aliphatic chain having 1-8 carbon atoms, wherein 1, 2, or 3 carbon atoms are optionally replaced with -NH- or -O-.
  • each R L6 is independently deuterium, halogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl. In some embodiments of a compound of Formula (XI), (XIa), or (XIb), each R L6 is independently deuterium or halogen.
  • L 6 is .
  • Ring B is cycloalkyl, heterocycloalkyl, aryl, heteroaryl;
  • R 1 and R 2 are independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R 3 is hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl;
  • R 3 and R 4 are taken together to form an optionally substituted ring
  • Ring A is cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; each optionally substituted with one or more R A ;
  • each X is independently -CR x - or -N-;
  • R x and R 5 are taken together to form ring D optionally substituted with one or more R D ;
  • Ring D is a cycloalkyl, heterocycloalkyl, aryl, or heteroaryl;
  • R 9 and R 10 are independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R 9 and R 10 are taken together with the nitrogen atom to which they are attached to form a
  • R 11 is C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl, C 1 -C 6 hydroxyalkyl, C 1 -C 6 aminoalkyl, C 2 - C 6 alkenyl, C 2 -C 6 alkynyl, cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently optionally substituted with one or more R 11a ;
  • each R a is independently C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl, C 1 -C 6 hydroxyalkyl,
  • each R c and R d is independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R c and R d are taken together with the nitrogen atom to which they are attached to form a
  • Ring B is cycloalkyl, heterocycloalkyl, aryl, heteroaryl;
  • R 1 and R 2 are independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R 3 is hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl;
  • R 3 and R 4 are taken together to form an optionally substituted ring
  • Ring A is cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; each optionally substituted with one or more R A ;
  • each X is independently -CR x - or -N-;
  • each R 8 is independently hydrogen, CN, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R 9 and R 10 are independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R 11 is C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl, C 1 -C 6 hydroxyalkyl, C 1 -C 6 aminoalkyl, C 2 - C 6 alkenyl, C 2 -C 6 alkynyl, cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently optionally substituted with one or more R 11a ;
  • each R a is independently C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl, C 1 -C 6 hydroxyalkyl,
  • each R c and R d is independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R c and R d are taken together with the nitrogen atom to which they are attached to form a
  • Ring B is cycloalkyl, heterocycloalkyl, aryl, heteroaryl;
  • R 1 and R 2 are independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R 3 is hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl;
  • R 3 and R 4 are taken together to form an optionally substituted ring
  • Ring A is cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; each optionally substituted with one or more R A ;
  • each X is independently -CR x - or -N-;
  • R x and R 5 are taken together to form ring D optionally substituted with one or more R D ;
  • Ring D is a cycloalkyl, heterocycloalkyl, aryl, or heteroaryl;
  • each R 8 is independently hydrogen, CN, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R 9 and R 10 are independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R 9 and R 10 are taken together with the nitrogen atom to which they are attached to form a
  • R 11 is C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl, C 1 -C 6 hydroxyalkyl, C 1 -C 6 aminoalkyl, C 2 - C 6 alkenyl, C 2 -C 6 alkynyl, cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently optionally substituted with one or more R 11a ;
  • each R a is independently C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl, C 1 -C 6 hydroxyalkyl,
  • each R c and R d is independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R c and R d are taken together with the nitrogen atom to which they are attached to form a
  • Ring B is cycloalkyl, heterocycloalkyl, aryl, heteroaryl;
  • R 1 and R 2 are independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R 3 is hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl;
  • R 3 and R 4 are taken together to form an optionally substituted ring
  • each X is independently -CR x - or -N-;
  • R x and R 5 are taken together to form ring D optionally substituted with one or more R D ;
  • Ring D is a cycloalkyl, heterocycloalkyl, aryl, or heteroaryl;
  • each R 8 is independently hydrogen, CN, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R 9 and R 10 are independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R 9 and R 10 are taken together with the nitrogen atom to which they are attached to form a
  • R 11 is C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl, C 1 -C 6 hydroxyalkyl, C 1 -C 6 aminoalkyl, C 2 - C 6 alkenyl, C 2 -C 6 alkynyl, cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl is independently optionally substituted with one or more R 11a ;
  • each R a is independently C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl, C 1 -C 6 hydroxyalkyl,
  • each R c and R d is independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R c and R d are taken together with the nitrogen atom to which they are attached to form a
  • Ring B is aryl or heteroaryl. In some embodiments of a compound of Formula (XII), Ring B is aryl. In some embodiments of a compound of Formula (XII), Ring B is phenyl. In some embodiments of a compound of Formula (XII), Ring B is heteroaryl. In some embodiments of a compound of Formula (XII), Ring B is 5- or 6-membered heteroaryl. In some embodiments of a compound of Formula (XII), Ring B is 6-membered heteroaryl. In some embodiments of a compound of Formula (XII), Ring B is pyridyl.
  • R 1 and R 2 are independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R 3 is hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl;
  • R 3 and R 4 are taken together to form an optionally substituted ring
  • Ring A is cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; each optionally substituted with one or more R A ;
  • each X is independently -CR x - or -N-;
  • R x and R 5 are taken together to form ring D optionally substituted with one or more R D ;
  • Ring D is a cycloalkyl, heterocycloalkyl, aryl, or heteroaryl;
  • each R 8 is independently hydrogen, CN, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R 9 and R 10 are independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R 9 and R 10 are taken together with the nitrogen atom to which they are attached to form a
  • R 11 is C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl, C 1 -C 6 hydroxyalkyl, C 1 -C 6 aminoalkyl, C 2 - C 6 alkenyl, C 2 -C 6 alkynyl, cycloalkyl, heterocycloalkyl, aryl, or heteroaryl; wherein each alkyl, alkenyl, alkynyl, cycloalky
  • each R a is independently C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl, C 1 -C 6 hydroxyalkyl,
  • each R c and R d is independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 deuteroalkyl,
  • R c and R d are taken together with the nitrogen atom to which they are attached to form a
  • -L-Ring A is absent.
  • Ring A is heterocycloalkyl or heteroaryl; each optionally substituted with one or more R A .
  • Ring A is a 5-membered heterocycloalkyl or a 5-membered heteroaryl; each optionally substituted with one or more R A .
  • Ring A is heteroaryl optionally substituted with one or more R A .
  • each R A is independently deuterium, halogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 deuteroalkyl. In some embodiments of a compound of Formula (XII) or (XII’), each R A is independently halogen or C 1 -C 6 alkyl. In some embodiments of a compound of Formula (XII) or (XII’), each R A is independently C 1 -C 6 alkyl.
  • each X is -N-. In some embodiments of a compound of Formula (XII), (XII’), (XIIa), (XIIb), or (XIIc) each X is -CR X -. In some embodiments of a compound of Formula (XII), (XII’), (XIIa), (XIIb), or (XIIc), two X are -N- and the other is -CR X -.
  • one X is -N- and the others are -CR X -.
  • each X is -CH-.
  • two X are -N- and the other is -CH-.
  • one X is -N- and the others are -CH-.
  • a compound of Formula (XII), (XII’), (XIIa), (XIIb), or (XIIc) is a compound of Formula (XII), (XII’), (XIIa), (XIIb), or (XIIc), (

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EP24203208.4A EP4461734B1 (en) 2018-10-22 2019-10-22 Tyk2 inhibitors and uses thereof
LTEPPCT/US2019/057485T LT3870579T (lt) 2018-10-22 2019-10-22 Tyk2 inhibitoriai ir jų naudojimas
PL19877015.8T PL3870579T3 (pl) 2018-10-22 2019-10-22 Inhibitory tyk2 i ich zastosowania
AU2019364336A AU2019364336B2 (en) 2018-10-22 2019-10-22 TYK2 inhibitors and uses thereof
HRP20250048TT HRP20250048T1 (hr) 2018-10-22 2019-10-22 Inhibitori tyk2 i njihova uporaba
KR1020217015306A KR102850357B1 (ko) 2018-10-22 2019-10-22 Tyk2 억제제 및 이의 용도
UAA202102676A UA130518C2 (uk) 2018-10-22 2019-10-22 Інгібітори tyk2 та шляхи їх застосування
MX2021004538A MX2021004538A (es) 2018-10-22 2019-10-22 Inhibidores de tyk2 y sus usos.
EP24203217.5A EP4480953B1 (en) 2018-10-22 2019-10-22 Tyk2 inhibitors and uses thereof
SG11202104017VA SG11202104017VA (en) 2018-10-22 2019-10-22 Tyk2 inhibitors and uses thereof
CN201980084885.9A CN113490664B (zh) 2018-10-22 2019-10-22 Tyk2抑制剂和其用途
ES19877015T ES3011855T3 (en) 2018-10-22 2019-10-22 Tyk2 inhibitors and uses thereof
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SI201930870T SI3870579T1 (sl) 2018-10-22 2019-10-22 Inhibitorji tyk2 in njihova uporaba
BR112021007679-4A BR112021007679A2 (pt) 2018-10-22 2019-10-22 inibidores de tyk2 e seus usos
SM20250070T SMT202500070T1 (it) 2018-10-22 2019-10-22 Inibitori di tyk2 e loro usi
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RS20241445A RS66346B1 (sr) 2018-10-22 2019-10-22 Inhibitori tyk2 i njihova upotreba
EP19877015.8A EP3870579B1 (en) 2018-10-22 2019-10-22 Tyk2 inhibitors and uses thereof
US16/938,183 US11053219B2 (en) 2018-10-22 2020-07-24 Substituted pyridines as TYK2 inhibitors
IL282487A IL282487B1 (en) 2018-10-22 2021-04-20 Tyk2 inhibitors and their use
US17/243,508 US12006306B2 (en) 2018-10-22 2021-04-28 Substituted pyridazines as TYK2 inhibitors
US17/713,646 US12060343B2 (en) 2018-10-22 2022-04-05 Substituted 1,2,4-triazoles as intermediates in the synthesis of TYK2 inhibitors
US17/891,817 US11731956B2 (en) 2018-10-22 2022-08-19 Substituted 1,2,4-triazoles as intermediates in the synthesis of TYK2 inhibitors
US18/335,262 US12351572B2 (en) 2018-10-22 2023-06-15 Substituted 1,2,4-triazoles as TYK2 inhibitors
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