WO2021173917A1 - Inhibitors of receptor interacting protein kinase i for the treatment of disease - Google Patents
Inhibitors of receptor interacting protein kinase i for the treatment of disease Download PDFInfo
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- WO2021173917A1 WO2021173917A1 PCT/US2021/019797 US2021019797W WO2021173917A1 WO 2021173917 A1 WO2021173917 A1 WO 2021173917A1 US 2021019797 W US2021019797 W US 2021019797W WO 2021173917 A1 WO2021173917 A1 WO 2021173917A1
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- Prior art keywords
- alkyl
- oxy
- cycloalkyl
- aryl
- heterocycloalkyl
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- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 1
- 239000005483 tyrosine kinase inhibitor Substances 0.000 description 1
- 229940121358 tyrosine kinase inhibitor Drugs 0.000 description 1
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- 238000010798 ubiquitination Methods 0.000 description 1
- 230000034512 ubiquitination Effects 0.000 description 1
- ZDPHROOEEOARMN-UHFFFAOYSA-N undecanoic acid Chemical compound CCCCCCCCCCC(O)=O ZDPHROOEEOARMN-UHFFFAOYSA-N 0.000 description 1
- 125000005500 uronium group Chemical group 0.000 description 1
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- JXLYSJRDGCGARV-XQKSVPLYSA-N vincaleukoblastine Chemical compound C([C@@H](C[C@]1(C(=O)OC)C=2C(=CC3=C([C@]45[C@H]([C@@]([C@H](OC(C)=O)[C@]6(CC)C=CCN([C@H]56)CC4)(O)C(=O)OC)N3C)C=2)OC)C[C@@](C2)(O)CC)N2CCC2=C1NC1=CC=CC=C21 JXLYSJRDGCGARV-XQKSVPLYSA-N 0.000 description 1
- UGGWPQSBPIFKDZ-KOTLKJBCSA-N vindesine Chemical compound C([C@@H](C[C@]1(C(=O)OC)C=2C(=CC3=C([C@]45[C@H]([C@@]([C@H](O)[C@]6(CC)C=CCN([C@H]56)CC4)(O)C(N)=O)N3C)C=2)OC)C[C@@](C2)(O)CC)N2CCC2=C1N=C1[C]2C=CC=C1 UGGWPQSBPIFKDZ-KOTLKJBCSA-N 0.000 description 1
- 229960004355 vindesine Drugs 0.000 description 1
- GBABOYUKABKIAF-IELIFDKJSA-N vinorelbine Chemical compound C1N(CC=2C3=CC=CC=C3NC=22)CC(CC)=C[C@H]1C[C@]2(C(=O)OC)C1=CC([C@]23[C@H]([C@@]([C@H](OC(C)=O)[C@]4(CC)C=CCN([C@H]34)CC2)(O)C(=O)OC)N2C)=C2C=C1OC GBABOYUKABKIAF-IELIFDKJSA-N 0.000 description 1
- 229960002066 vinorelbine Drugs 0.000 description 1
- CILBMBUYJCWATM-PYGJLNRPSA-N vinorelbine ditartrate Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O.OC(=O)[C@H](O)[C@@H](O)C(O)=O.C1N(CC=2C3=CC=CC=C3NC=22)CC(CC)=C[C@H]1C[C@]2(C(=O)OC)C1=CC([C@]23[C@H]([C@@]([C@H](OC(C)=O)[C@]4(CC)C=CCN([C@H]34)CC2)(O)C(=O)OC)N2C)=C2C=C1OC CILBMBUYJCWATM-PYGJLNRPSA-N 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
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- A61P27/02—Ophthalmic agents
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—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
- 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
- C07D213/61—Halogen atoms or nitro radicals
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- C07D213/00—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
- 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
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
-
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/26—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
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- 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
- C07D401/02—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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- C—CHEMISTRY; METALLURGY
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- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—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
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- 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
- C07D487/04—Ortho-condensed systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
- C07D491/107—Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
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- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
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- C—CHEMISTRY; METALLURGY
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
Definitions
- RIPKI consists of an N-terminal kinase domain, a RHIM (RIP homotypic interaction motif) domain, and a death domain, which collectively undergo extensive post-translational modification in response to signaling through various receptors such as tumor necrosis factor ⁇ receptors (TNFRs), toll-like receptors, NOD-like receptor, and others.
- TNFRs tumor necrosis factor ⁇ receptors
- NOD-like receptor NOD-like receptor
- RIPKI has been most extensively studied in the context of TNFRI signaling, which triggers its recruitment to the C-terminal domain of the receptor via the protein TRADD (TNF receptor associated death domain protein).
- RIPKI is ubiquitinated by the E3 ubiquitin ligases TNF receptor-associated factor 2 (TRAF2) or TRAF5 and the cellular inhibitor of apoptosis proteins (cIAPs) cIAPI and cIAP2.
- TNF receptor-associated factor 2 TRAF2
- cIAPs apoptosis proteins
- cIAPI and cIAP2 apoptosis proteins
- This molecular assembly is known as complex I. Cylindromatosis (CYLD) then mediates the deubiquitination of RIPKI to allow assembly of complex IIb, also known as the necrosome.
- the necrosome consists of the RIPKI homolog RIPK3 and the pseudokinase MLKL. The assembly and function of the necrosome is inhibited by caspase 8 such that only when caspase 8 activity is blocked is the necrosome functional.
- necrosome causes necroptosis, an inflammatory form of programmed cell death in which membrane lysis causes the release of cellular contents into the extracellular space.
- RIPKI can also, in different contexts, regulate apoptosis and inflammation. When cIAPs are inhibited so that RIPKI ubiquitination does not occur, RIPKI participates in apoptosis.
- Ubiquitinated RIPKI can also recruit NF-KB essential modulator (NEMO) and TAKI binding protein 2 or 3 (TAB2/3), leading to activation of inhibitor of kappa B (IKB) kinase beta (IKK ) and transforming growth factor beta (TGF )-activated kinase 1 (TAKI), which in tum promotes the NF-KB pro-inflammatory or pro-survival gene expression programs.
- NEMO essential modulator
- TAB2/3 TAKI binding protein 2 or 3
- TGF transforming growth factor beta
- RIPKl Given its role in inflammation, RIPKl has been implicated in many diseases featuring chronic and acute inflammatory signaling, including viral infections, sepsis, retinal degeneration, traumatic brain injury, ischemic stroke, intracerebral hemorrhage, amyotrophic lateral sclerosis, acute kidney injury, myocardial reperfusion injury, Alzheimer's disease, ulcerative colitis, osteoarthritis, and others.
- RIPKl kinase inhibitors such as necrostatin-1 have shown to be effective, leading to the development of such molecules for clinical trials in a number of indications.
- R 1 is chosen from CN, halo, hydroxy, alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, (cycloalkyl)alkyl, (heterocycloalkyl)alkyl, (aryl)alkyl, and (heteroaryl)alkyl, any one of which is optionally substituted with one or more R 6 ;
- R 2 and R 3 are independently chosen from H, halo, cyano, alkyl, (alkyl)oxy, (alkyl)thio, (alkyl)sulfonimidoyl, (alkyl)sulfonyl, cycloalkyl, and (cycloalkyl)oxy, any one of which is optionally substituted with one or more R 7 , or R 2 and R 3
- W is chosen from CH, CR 5 , and N;
- R 1 is chosen from CN, halo, hydroxy, alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, (cycloalkyl)alkyl, (heterocycloalkyl)alkyl, (aryl)alkyl, and (heteroaryl)alkyl, any one of which is optionally substituted with one or more R 6 ;
- R 2 and R 3 are independently chosen from H, halo, cyano, alkyl, (alkyl)oxy, cycloalkyl, and (cycloalkyl)oxy, any one of which is optionally substituted with one or more R 7 , or R 2 and R 3 , together with the intervening two carbons, combine to form a 5-7 membered cycloalkyl, heterocycloalkyl, aryl, or heteroaryl ring, any one of which is optionally substituted with one or more
- compositions comprising one or more compounds, salts or tautomers, disclosed herein together with a pharmaceutically acceptable carrier, as well as methods of making and using the compounds, salts, or tautomers, and compositions.
- Certain embodiments provide methods for inhibiting RIPK1.
- Certain embodiments provide methods for treating a RIPK1-mediated disorder in a patient in need of such treatment, comprising administering to said patient a therapeutically effective amount of a compound, or a salt or tautomer thereof, or composition as disclosed herein.
- use of certain compounds, salts or tautomers disclosed herein for use in the manufacture of a medicament for the treatment of a disease or condition ameliorated by the inhibition of RIPK1.
- R 1 is chosen from CN, halo, hydroxy, alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, (cycloalkyl)alkyl, (heterocycloalkyl)alkyl, (aryl)alkyl, and (heteroaryl)alkyl, any one of which is optionally substituted with one or more R 6 ;
- R 2 and R 3 are independently chosen from H, halo, cyano, alkyl, (alkyl)oxy, (alkyl)thio, (alkyl)sulfonimidoyl, (alkyl)sulfonyl, cycloalkyl, and (cycloalkyl)oxy, any one of which is optionally substituted with one or more R 7 , or R 2 and R 3 , together with the intervening two carbons, combine to
- R 1 is chosen from CN, halo, hydroxy, alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, (cycloalkyl)alkyl, (heterocycloalkyl)alkyl, (aryl)alkyl, and (heteroaryl)alkyl, any one of which is optionally substituted with one or more R 6 ;
- R 2 and R 3 are independently chosen from H, halo, cyano, alkyl, (alkyl)oxy, cycloalkyl, and (cycloalkyl)oxy, any one of which is optionally substituted with one or more R 7 , or R 2 and R 3 , together with the intervening two carbons, combine to form a 5-7 membered cycloalkyl, heterocycloalkyl, aryl, or heteroaryl ring, any one of which is optionally substituted with one or more R 8 and optionally fused with a 6- membered
- R 4 is chosen from C1-6alkyl, C3-7cycloalkyl, 4- to 11- membered heterocycloalkyl, C 6-14 aryl, 5- to 14-membered heteroaryl, (C 3-7 cycloalkyl)C 1- 6alkyl, (4- to 11-membered heterocycloalkyl)C1-6alkyl, (C6-10aryl)C1-6alkyl, and (5- to 14- membered heteroaryl)C 1-6 alkyl, any one of which is optionally substituted with one or more R 10 .
- R 4 is chosen from C 1-6 alkyl, C 3-7 cycloalkyl, 4- to 11-membered heterocycloalkyl, C 6-14 aryl, 5- to 14-membered heteroaryl, (C 3-7 cycloalkyl)methyl, (4- to 11- membered heterocycloalkyl)methyl, (C6-10aryl)methyl, (5- to 14-membered heteroaryl)methyl, any one of which is optionally substituted with one or more R 10 .
- R 4 is chosen from C1-6alkyl, cyclopropyl, cyclobutyl, phenyl, 2,3,4,5- tetrahydro-1H-benzo[b]azepinyl, 2,3,4,5-tetrahydrobenzo[b][1,4]oxazepinyl, 2,3,4,5- tetrahydropyrido[3,2-b][1,4]oxazepin-3-yl, 2,3,4,5-tetrahydro-1H-pyrido[3,4-b]azepin-3-yl, and 5,6,7,8-tetrahydro-4H-pyrazolo[1,5-a][1,3]diazepin-6-yl, any one of which is optionally substituted with one or more R 10 .
- R 4 is optionally substituted with one, two, or three R 10 . In certain embodiments, R 4 is optionally substituted with one or two R 10 . In certain embodiments, R 4 is substituted with one or two R 10 . [011] In certain embodiments, [012] In certain embodiments: R 4 is chosen from:
- each V is independently chosen from CH, C(R 10 ), and N; W 3 is chosen from CH 2 , NH, O, and S; R 10g is chosen from H, alkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl, any one of which is optionally substituted with one or more R 11 ; each R 10 is independently chosen from CN, halo, hydroxy, oxo, alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, (cycloalkyl)CH 2 , (heterocycloalkyl)CH 2 , (aryl)CH 2 , (heteroaryl)CH 2 , (alkyl)SO 2 , (cycloalkyl)SO 2 , (heterocycloalkyl)SO 2 , (aryl)SO 2 , (heteroaryl)SO 2 , (alkyl)NH, (cycloalkyl)NH, (heterocycloal
- R 4 is chosen from: each V is independently chosen from CH, C(R 10 ), and N; W 3 is chosen from CH 2 , NH, O, and S; R 10g is chosen from H, alkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl, any one of which is optionally substituted with one or more R 11 ; each R 10 is independently chosen from CN, halo, hydroxy, oxo, alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, (alkyl)oxy, (cycloalkyl)oxy, (heterocycloalkyl)oxy, (aryl)oxy, and (heteroaryl)oxy, any one of which is optionally substituted with one or more R 11 ; each R 11 is independently chosen from CN, halo, hydroxy, oxo, alkyl, cycloalkyl, heterocycloalkyl, alkylsul
- R 10g is chosen from H, alkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl, any one of which is optionally substituted with one or more R 11 ; each R 10 is independently chosen from CN, halo, hydroxy, oxo, alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, (cycloalkyl)CH 2 , (heterocycloalkyl)CH 2 , (aryl)CH 2 , (heteroaryl)CH 2 , (alkyl)SO 2 , (cycloalkyl)SO 2 , (heterocycloalkyl)SO 2 , (aryl)SO 2 , (heteroaryl)SO 2 , (alkyl)NH, (cycloalkyl)NH, (heterocycloalkyl)NH, (aryl)NH, (heteroaryl)NH, (alkyl)oxy, (cycloalkyl)
- R 10g is chosen from H, alkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl, any one of which is optionally substituted with one or more R 11 ; each R 10 is independently chosen from CN, halo, hydroxy, oxo, alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, (alkyl)oxy, (cycloalkyl)oxy, (heterocycloalkyl)oxy, (aryl)oxy, and (heteroaryl)oxy, any one of which is optionally substituted with one or more R 11 ; each R 11 is independently chosen from CN, halo, hydroxy, oxo, alkyl, cycloalkyl, heterocycloalkyl, alkylsulfonyl, haloalkylsulfonyl, aryl, heteroaryl, (alkyl)oxy, (cycloalkyl)oxy, (heterocyclo
- R 10g is chosen from H, alkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl, any one of which is optionally substituted with one or more R 11 ; each R 10 is independently chosen from CN, halo, hydroxy, oxo, alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, (cycloalkyl)CH 2 , (heterocycloalkyl)CH 2 , (aryl)CH 2 , (heteroaryl)CH 2 , (alkyl)SO 2 , (cycloalkyl)SO 2 , (heterocycloalkyl)SO 2 , (aryl)SO 2 , (heteroaryl)SO 2 , (alkyl)NH, (cycloalkyl)NH, (heterocycloalkyl)NH, (aryl)NH, (heteroaryl)NH, (alkyl)oxy, (cycloalkyl
- R 10g is chosen from H, alkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl, any one of which is optionally substituted with one or more R 11 ; each R 10 is independently chosen from CN, halo, hydroxy, oxo, alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, (alkyl)oxy, (cycloalkyl)oxy, (heterocycloalkyl)oxy, (aryl)oxy, and (heteroaryl)oxy, any one of which is optionally substituted with one or more R 11 ; each R 11 is independently chosen from CN, halo, hydroxy, oxo, alkyl, cycloalkyl, heterocycloalkyl, alkylsulfonyl, haloalkylsulfonyl, aryl, heteroaryl, (alkyl)oxy, (cycloalkyl)
- R 10g is chosen from H and alkyl. In certain embodiments, R 10g is chosen from H and C 1-4 alkyl. In certain embodiments, R 10g is chosen from H, CH 3 , CD3, CH 2 CH 3 , CH(CH 3 )2, and C(CH 3 )3. In certain embodiments, R 10g is chosen from H, CH 3 , and CD3. In certain embodiments, R 10g is CH 3 . [020] In certain embodiments, R 10g is chosen from H, methyl, ethyl, and 2-propyl. In certain embodiments, R 10g is chosen from H, methyl, and methyl-d3. In certain embodiments, R 10g is methyl. [021] In certain embodiments, R 4 is In certain embodiments, R 4 is . [022] In certain embodiments: R 4 is chosen from
- a compound of structural Formula (II): or a salt or tautomer thereof wherein: m is chosen from 0, 1, and 2; W is chosen from CH, CR 5 , and N; R 1 is chosen from CN, halo, hydroxy, alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, (cycloalkyl)alkyl, (heterocycloalkyl)alkyl, (aryl)alkyl, and (heteroaryl)alkyl, any one of which is optionally substituted with one or more R 6 ; R 2 and R 3 are independently chosen from H, halo, cyano, alkyl, (alkyl)oxy, (alkyl)thio, (alkyl)sulfonimidoyl, (alkyl)sulfonyl, cycloalkyl, and (cycloalkyl)oxy, any one of which is optionally substituted with one or
- a compound of structural Formula (II): or a salt or tautomer thereof wherein: m is chosen from 0, 1, and 2; W is chosen from CH, CR 5 , and N; R 1 is chosen from CN, halo, hydroxy, alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, (cycloalkyl)alkyl, (heterocycloalkyl)alkyl, (aryl)alkyl, and (heteroaryl)alkyl, any one of which is optionally substituted with one or more R 6 ; R 2 and R 3 are independently chosen from H, halo, cyano, alkyl, (alkyl)oxy, cycloalkyl, and (cycloalkyl)oxy, any one of which is optionally substituted with one or more R 7 , or R 2 and R 3 , together with the intervening two carbons, combine to form a 5-7 membered cyclo
- R 4a is chosen from C1-6alkyl, C3-7cycloalkyl, 4- to 11- membered heterocycloalkyl, C 6-14 aryl, and 5- to 14-membered heteroaryl, any one of which is optionally substituted with one or more R 10 .
- R 4a is chosen from C1- 6 alkyl, cyclopropyl, cyclobutyl, 2,3,4,5-tetrahydro-1H-benzo[b]azepinyl, 2,3,4,5-tetrahydro- benzo[b][1,4]oxazepinyl, phenyl, pyrrolyl, imidazolyl, pyrazolyl, thiazolyl, isothiazolyl, oxazolyl, isoxazoyl, 1,2,3-oxadiazolyl, 1,2,3-thiadiazolyl, 1,2,4-oxadiazolyl, 1,2,4- thiadiazolyl, pyridinyl, pyrazinyl, pyrimidinyl, pyridazinyl, quinolinyl, isoquinolinyl, indolinyl, acridinyl, pyrazolo[1,5-a]pyridinyl, benzo[d]
- R 4a is chosen from 2,3,4,5-tetrahydro-1H-benzo[b]azepinyl, 2,3,4,5- tetrahydrobenzo[b][1,4]oxazepinyl, phenyl, pyrrolyl, imidazolyl, pyrazolyl, thiazolyl, isothiazolyl, oxazolyl, isoxazoyl, 1,2,3-oxadiazolyl, 1,2,3-thiadiazolyl, 1,2,4-oxadiazolyl, 1,2,4-thiadiazolyl, pyridinyl, pyrazinyl, pyrimidinyl, pyridazinyl, quinolinyl, isoquinolinyl, indolinyl, acridinyl, pyrazolo[1,5-a]pyridinyl, benzo[d]thiazolyl, 1H-benzo[d]imidazolyl, and 1H-
- each V is independently chosen from CH, C(R 10 ), and N; W 3 is chosen from CH 2 , NH, O, and S; R 10g is chosen from H, alkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl, any one of which is optionally substituted with one or more R 11 ; each R 10 is independently chosen from CN, halo, hydroxy, oxo, alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, (cycloalkyl)CH 2 , (heterocycloalkyl)CH 2 , (aryl)CH 2 , (heteroaryl)CH 2 , (alkyl)SO 2 , (cycloalkyl)SO 2 , (heterocycloalkyl)SO 2 , (aryl)SO 2 , (heteroaryl)SO 2 , (alkyl)NH, (cycloalkyl)NH, (heterocycloal
- R 4a is chosen from: each V is independently chosen from CH, C(R 10 ), and N; W 3 is chosen from CH 2 , NH, O, and S; R 10g is chosen from H, alkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl, any one of which is optionally substituted with one or more R 11 ; each R 10 is independently chosen from CN, halo, hydroxy, oxo, alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, (alkyl)oxy, (cycloalkyl)oxy, (heterocycloalkyl)oxy, (aryl)oxy, and (heteroaryl)oxy, any one of which is optionally substituted with one or more R 11 ; each R 11 is independently chosen from CN, halo, hydroxy, oxo, alkyl, cycloalkyl, heterocycloalkyl, alkyls
- R 10g is chosen from H, alkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl, any one of which is optionally substituted with one or more R 11 ; each R 10 is independently chosen from CN, halo, hydroxy, oxo, alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, (cycloalkyl)CH 2 , (heterocycloalkyl)CH 2 , (aryl)CH 2 , (heteroaryl)CH 2 , (alkyl)SO 2 , (cycloalkyl)SO 2 , (heterocycloalkyl)SO 2 , (aryl)SO 2 , (heteroaryl)SO 2 , (alkyl)NH, (cycloalkyl)NH, (heterocycloalkyl)NH, (aryl)NH, (heteroaryl)NH, (alkyl)oxy, (cycloalkyl)
- R 10g is chosen from H, alkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl, any one of which is optionally substituted with one or more R 11 ; each R 10 is independently chosen from CN, halo, hydroxy, oxo, alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, (alkyl)oxy, (cycloalkyl)oxy, (heterocycloalkyl)oxy, (aryl)oxy, and (heteroaryl)oxy, any one of which is optionally substituted with one or more R 11 ; each R 11 is independently chosen from CN, halo, hydroxy, oxo, alkyl, cycloalkyl, heterocycloalkyl, alkylsulfonyl, haloalkylsulfonyl, aryl, heteroaryl, (alkyl)oxy, (cycloalkyl)
- R 10g is chosen from H and alkyl. In certain embodiments, R 10g is chosen from H and C 1-4 alkyl. In certain embodiments, R 10g is chosen from H, CH 3 , CD 3 , CH 2 CH 3 , CH(CH 3 )2, and C(CH 3 )3. In certain embodiments, R 10g is chosen from H, CH 3 , and CD 3 . In certain embodiments, R 10g is CH 3 . [032] In certain embodiments, R 10g is chosen from H, methyl, ethyl, and 2-propyl. In certain embodiments, R 10g is chosen from H, methyl, and methyl-d 3 . In certain embodiments, R 10g is methyl. [033] Also provided herein is a compound of structural Formula (III):
- m is chosen from 0, 1, and 2; W is chosen from CH, CR 5 , and N; W 2 is chosen from CHR 10a , CR 10a , NR 10a , N, O, and S; W 3 is chosen from CHR 10b , CR 10b , NR 10b , N, O, and S; W 4 is chosen from a bond, CHR 10c , CR 10c , NR 10c , N, O, and S; W 5 is chosen from CHR 10d , CR 10d , NR 10d , N, O, and S; W 6 is chosen from CHR 10e , CR 10e , NR 10e , N, O, and S; W 7 is chosen from CHR 10f , CR 10f , NR 10f , N, O, and S; W 2 , W 3 , W 4 , W 5 , W 6 , and W 7 , together with the intervening carbon, combine
- m is chosen from 0, 1, and 2; W is chosen from CH, CR 5 , and N; W 2 is chosen from CHR 10a , CR 10a , NR 10a , N, O, and S; W 3 is chosen from CHR 10b , CR 10b , NR 10b , N, O, and S; W 4 is chosen from a bond, CHR 10c , CR 10c , NR 10c , N, O, and S; W 5 is chosen from CHR 10d , CR 10d , NR 10d , N, O, and S; W 6 is chosen from CHR 10e , CR 10e , NR 10e , N, O, and S; W 7 is chosen from CHR 10f , CR 10f , NR 10f , N, O, and S; W 2 , W 3 , W 4 , W 5 , W 6 , and W 7 , together with the intervening carbon, combine
- W 6 is chosen from NH and N(CH 3 ).
- R 10c and R 10d combine, together with the intervening two atoms, to form phenyl or a 5- or 6-membered heteroaryl, any one of which is optionally substituted with one or more R 10 .
- R 10c and R 10d combine, together with the intervening two atoms, to form phenyl or a 6-membered heteroaryl, either one of which is optionally substituted with one or more R 10 .
- R 10c and R 10d combine, together with the intervening two atoms, to form phenyl, pyridinyl, pyridazinyl, pyrimidinyl, or pyrazinyl, any one of which is optionally substituted with one or two R 10 .
- R 10c and R 10d combine, together with the intervening two atoms, to form phenyl or pyridinyleither one of which is optionally substituted with one or two R 10 .
- each R 4b is independently chosen from H and C1-6alkyl. In certain embodiments, each R 4b is independently chosen from H, methyl, and ethyl.
- each R 4b is independently chosen from H and methyl. In certain embodiments, at most one R 4b is not H. In certain embodiments, R 4b is H. [039] In certain embodiments, m is chosen from 0 and 1. In certain embodiments, m is 0.
- R 10a , R 10b , R 10c , R 10d , R 10e , and R 10f are independently chosen from H, CN, halo, hydroxy, oxo, C1-6alkyl, C3-7cycloalkyl, 5- to 14-membered heterocycloalkyl, C 6-14 aryl, 5- to 14-membered heteroaryl, (C 1-6 alkyl)oxy, (C 3- 7cycloalkyl)oxy, (5- to 14-membered heterocycloalkyl)oxy, (C6-14aryl)oxy, and (5- to 14- membered heteroaryl)oxy, any one of which is optionally substituted with one or two R 11 .
- R 10a , R 10b , R 10c , R 10d , R 10e , and R 10f are independently chosen from H, CN, halo, hydroxy, oxo, methyl, ethyl, cyclopropyl, and cyclobutyl, any one of which is optionally substituted with one or two R 11 .
- R 10a , R 10b , R 10c , R 10d , R 10e , and R 10f are optionally substituted with one R 11 .
- at most one of R 10a , R 10b , R 10c , R 10d , R 10e , and R 10f is substituted with an R 11 .
- R 10a , R 10b , R 10c , R 10d , R 10e , and R 10f are substituted with an R 11 .
- R 10a , R 10b , R 10c , R 10d , R 10e , and R 10f are independently chosen from H, CN, halo, hydroxy, oxo, and methyl.
- W 4 is chosen from CHR 10c , CR 10c , NR 10c , N, O, and S.
- V 1 is chosen from a bond, CH, CR 10 , N, NH, NR 10 , O, and S;
- V 2 , V 3 , and V 4 are independently chosen from CH, CR 10 , N, NH, NR 10 , O, and S;
- V 1 , V 2 , V 3 , and V 4 together with the intervening two carbons, combine to form a 5- or 6-membered aryl or heteroaryl;
- W is chosen from CH, CR 5 , and N;
- W 2 and W 3 are independently chosen from CH 2 , CHR 10 , NH, O, and S;
- R 1 is chosen from CN, halo, hydroxy, alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, (cycloalkyl)alkyl, (heterocycloalkyl)alkyl, (aryl
- V 1 is chosen from a bond, CH, CR 10 , N, NH, NR 10 , O, and S;
- V 2 , V 3 , and V 4 are independently chosen from CH, CR 10 , N, NH, NR 10 , O, and S;
- V 1 , V 2 , V 3 , and V 4 together with the intervening two carbons, combine to form a 5- or 6-membered aryl or heteroaryl;
- W is chosen from CH, CR 5 , and N;
- W 2 and W 3 are independently chosen from CH 2 , CHR 10 , NH, O, and S;
- R 1 is chosen from CN, halo, hydroxy, alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, (cycloalkyl)alkyl, (heterocycloalkyl)alkyl, (aryl
- W 2 is CH(R 10 ). In certain embodiments, W 2 is CH 2 . [052] In certain embodiments, W 2 is NH. In certain embodiments, W 2 is O. In certain embodiments, W 2 is S. [053] In certain embodiments, W 3 is CH(R 10 ). In certain embodiments, W 3 is CH 2 . [054] In certain embodiments, W 3 is NH. In certain embodiments, W 3 is O. In certain embodiments, W 3 is S.
- V 1 is chosen from a bond, CH, CR 10 , N, NH, NR 10 , O, and S;
- V 2 , V 3 , and V 4 are independently chosen from CH, CR 10 , N, NH, NR 10 , O, and S;
- V 1 , V 2 , V 3 , and V 4 together with the intervening two carbons, combine to form a 5- or 6-membered aryl or heteroaryl;
- W is chosen from CH, CR 5 , and N;
- R 1 is chosen from CN, halo, hydroxy, alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, (cycloalkyl)alkyl, (heterocycloalkyl)alkyl, (aryl)alkyl, and (heteroaryl)alkyl, any one of which is optionally substitute
- V 1 is chosen from a bond, CH, CR 10 , N, NH, NR 10 , O, and S;
- V 2 , V 3 , and V 4 are independently chosen from CH, CR 10 , N, NH, NR 10 , O, and S;
- V 1 , V 2 , V 3 , and V 4 together with the intervening two carbons, combine to form a 5- or 6-membered aryl or heteroaryl;
- W is chosen from CH, CR 5 , and N;
- R 1 is chosen from CN, halo, hydroxy, alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, (cycloalkyl)alkyl, (heterocycloalkyl)alkyl, (aryl)alkyl, and (heteroaryl)alkyl, any one of which is optionally substituted with one or more R 6 ;
- R 2 and R 3 are independently chosen from H,
- R 10g is chosen from H and alkyl. In certain embodiments, R 10g is chosen from H and C1-4alkyl. In certain embodiments, R 10g is chosen from H, CH 3 , CD3, CH 2 CH 3 , CH(CH 3 )2, and C(CH 3 )3. In certain embodiments, R 10g is chosen from H, CH 3 , and CD3. In certain embodiments, R 10g is CH 3 . [058] In certain embodiments, R 10g is chosen from H, methyl, ethyl, and 2-propyl. In certain embodiments, R 10g is chosen from H, methyl, and methyl-d3. In certain embodiments, R 10g is methyl.
- R 10g is H.
- V 1 , V 2 , V 3 , and V 4 are independently chosen from CH, CR 10 , and N; and V 1 , V 2 , V 3 , and V 4 , together with the intervening two carbons, combine to form a 6- membered aryl or heteroaryl.
- V 1 , V 2 , V 3 , and V 4 are independently chosen from CH and N.
- exactly one of V 1 , V 2 , V 3 , and V 4 is N.
- exactly two of V 1 , V 2 , V 3 , and V 4 are N.
- V 1 , V 2 , V 3 , and V 4 are chosen from CH and CR 10 ; and V 1 , V 2 , V 3 , and V 4 , together with the intervening two carbons, combine to form a 6- membered aryl.
- V 1 is a bond;
- V 2 , V 3 , and V 4 are independently chosen from CH, CR 10 , N, NH, NR 10 , O, and S; and V 2 , V 3 , and V 4 , together with the intervening two carbons, combine to form a 5- membered heteroaryl.
- V 2 , V 3 , and V 4 are chosen from O and S.
- V 2 , V 3 , and V 4 are independently chosen from CH, CR 10 , N, NH, and NR 10 .
- exactly one of V 2 , V 3 , and V 4 is chosen from N, NH, and NR 10 .
- exactly two of V 2 , V 3 , and V 4 are chosen from N, NH, and NR 10 .
- each R 10 is independently chosen from CN, halo, hydroxy, oxo, alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, (alkyl)oxy, (cycloalkyl)oxy, (heterocycloalkyl)oxy, (aryl)oxy, and (heteroaryl)oxy, any one of which is optionally substituted with one or more R 11 .
- each R 10 is independently chosen from CN, halo, hydroxy, oxo, C1-6alkyl, C3-7cycloalkyl, 5- to 14-membered heterocycloalkyl, C6-14aryl, 5- to 14-membered heteroaryl, (C 3-7 cycloalkyl)CH 2 , (5- to 14-membered heterocycloalkyl)CH 2 , (C6-14aryl)CH 2 , and (5- to 14-membered heteroaryl)CH 2 , (C1-6alkyl)SO 2 , (C3-7cycloalkyl)SO 2 , (5- to 14-membered heterocycloalkyl)SO 2 , (C 6-14 aryl)SO 2 , (5- to 14-membered heteroaryl)SO 2 , (C1-6alkyl)NH, (C3-7cycloalkyl)NH, (5- to 14-membered heterocycloalkyl)NH, (C 6-14 ary
- each R 10 is independently chosen from C1-6alkyl, C3- 7cycloalkyl, 5- to 14-membered heterocycloalkyl, C6-14aryl, 5- to 14-membered heteroaryl, (C3-7cycloalkyl)CH 2 , (5- to 14-membered heterocycloalkyl)CH 2 , (C6-14aryl)CH 2 , and (5- to 14-membered heteroaryl)CH 2 , (C1-6alkyl)SO 2 , (C3-7cycloalkyl)SO 2 , (5- to 14-membered heterocycloalkyl)SO 2 , (C6-14aryl)SO 2 , (5- to 14-membered heteroaryl)SO 2 , (C1-6alkyl)NH, (C3-7cycloalkyl)NH, (5- to 14-membered heterocycloalkyl)NH, (C6-14aryl)NH, and (5- to 14- membered heteroaryl)
- each R 10 is independently chosen from C1-6alkyl, C3- 7 cycloalkyl, 5- to 14-membered heterocycloalkyl, C 6-14 aryl, 5- to 14-membered heteroaryl, (C1-6alkyl)oxy, (C3-7cycloalkyl)oxy, (5- to 14-membered heterocycloalkyl)oxy, (C6- 14 aryl)oxy, and (5- to 14-membered heteroaryl)oxy, any one of which is optionally substituted with one or two R 11 .
- each R 10 is independently chosen from C 1-6 alkyl, C 3- 7cycloalkyl, 5- to 14-membered heterocycloalkyl, C6-14aryl, and 5- to 14-membered heteroaryl, any one of which is optionally substituted with one or two R 11 .
- each R 10 is independently chosen from C1-6alkyl, C3- 7cycloalkyl, and 5- to 14-membered heterocycloalkyl, any one of which is optionally substituted with one or two R 11 .
- each R 10 is optionally substituted with one R 11 .
- each R 10 is substituted with one R 11 .
- each R 10 is unsubstituted with an R 11 .
- each R 10 is independently chosen from H, CH 3 , CD 3 , F,
- each R 10 is independently chosen from CN, halo, hydroxy, and oxo.
- each R 10 is independently chosen from CN and halo.
- each R 10 is independently chosen from F and Cl. [085] In certain embodiments, each R 10 is independently chosen from F, Cl, Br, CN, CH 3 , CH 2 CH 3 , CH(CH 3 )2, C(CH 3 )3, OCH 3 , and CF3.
- each R 10 is independently chosen from CH 3 and CH 2 CH 3 .
- a compound of structural Formula (V): or a salt or tautomer thereof wherein: W is chosen from CH, CR 5 , and N; W 2 is chosen from CR 10a and N; W 3 is chosen from CR 10b and N; W 5 is chosen from CR 10d and N; W 6 is chosen from CR 10e and N; W 7 is chosen from CR 10f and N; R 1 is chosen from CN, halo, hydroxy, alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, (cycloalkyl)alkyl, (heterocycloalkyl)alkyl, (aryl)alkyl, and (heteroaryl)alkyl, any one of which is optionally substituted with one or more R 6 ; R 2 and R 3 are independently chosen from H, halo, cyano, alkyl, (V): or a salt or tautomer
- W is chosen from CH, CR 5 , and N; W 2 is chosen from CR 10a and N; W 3 is chosen from CR 10b and N; W 5 is chosen from CR 10d and N; W 6 is chosen from CR 10e and N; W 7 is chosen from CR 10f and N; R 1 is chosen from CN, halo, hydroxy, alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, (cycloalkyl)alkyl, (heterocycloalkyl)alkyl, (aryl)alkyl, and (heteroaryl)alkyl, any one of which is optionally substituted with one or more R 6 ; R 2 and R 3 are independently chosen from H, halo, cyano, alkyl, (alkyl)oxy, cycloalkyl, and (cycloalkyl)
- W is chosen from N, CH and C(Cl). In certain embodiments, W is chosen from CH and CR 5 . In certain embodiments, R 5 is chosen from H, CN, halo, hydroxy, C1-6alkyl, and (C1-6alkyl)oxy. In certain embodiments, R 5 is chosen from H, CN, F, Cl, Br, and hydroxy. In certain embodiments, R 5 is chosen from H and Cl. In certain embodiments, R 5 is H. In certain embodiments, W is N.
- R 10a , R 10b , R 10d , R 10e , and R 10f are independently chosen from H, CN, halo, hydroxy, oxo, C 1-6 alkyl, C 3-7 cycloalkyl, 5- to 14-membered heterocycloalkyl, C6-14aryl, 5- to 14-membered heteroaryl, (C1-6alkyl)oxy, (C3- 7cycloalkyl)oxy, (5- to 14-membered heterocycloalkyl)oxy, (C6-14aryl)oxy, and (5- to 14- membered heteroaryl)oxy, any one of which is optionally substituted with one or two R 11 .
- R 10a , R 10b , R 10d , R 10e , and R 10f are independently chosen from H, C1- 6 alkyl, C 3-7 cycloalkyl, 5- to 14-membered heterocycloalkyl, C 6-14 aryl, 5- to 14-membered heteroaryl, (C1-6alkyl)oxy, (C3-7cycloalkyl)oxy, (5- to 14-membered heterocycloalkyl)oxy, (C 6-14 aryl)oxy, and (5- to 14-membered heteroaryl)oxy, any one of which is optionally substituted with one or two R 11 .
- R 10a , R 10b , R 10d , R 10e , and R 10f are independently chosen from H, CN, halo, hydroxy, C 1-6 alkyl, C 3-7 cycloalkyl, 5- to 14- membered heterocycloalkyl, C 6-14 aryl, and 5- to 14-membered heteroaryl, any one of which is optionally substituted with one or two R 11 .
- R 10a , R 10b , R 10d , R 10e , and R 10f are independently chosen from H, C1-6alkyl, C3-7cycloalkyl, and 5- to 14-membered heterocycloalkyl, any one of which is optionally substituted with one R 11 .
- R 10a , R 10b , R 10d , R 10e , and R 10f are independently chosen from H, CN, halo, hydroxy, and oxo.
- R 10a , R 10b , R 10d , R 10e , and R 10f is not H. In certain embodiments, at least two of R 10a , R 10b , R 10d , R 10e , and R 10f are not H.
- At least one of R 10a , R 10b , R 10d , R 10e , and R 10f is halo. In certain embodiments, at least two of R 10a , R 10b , R 10d , R 10e , and R 10f are halo. [095] In certain embodiments, at least one of R 10a , R 10b , R 10d , R 10e , and R 10f is Cl. [096] In certain embodiments, at least one of R 10a , R 10b , R 10d , R 10e , and R 10f is Br.
- none of W 2 , W 3 , W 5 , W 6 , and W 7 is N.
- at least one of W 2 , W 3 , W 5 , W 6 , and W 7 is N.
- exactly one of W 2 , W 3 , W 5 , W 6 , and W 7 is N.
- exactly two of W 2 , W 3 , W 5 , W 6 , and W 7 are N.
- W 2 is N.
- W 3 is N.
- W 5 is N.
- R 10a , R 10b , R 10d , R 10e , and R 10f are independently chosen from H, CN, halo, hydroxy, C1-6alkyl, C3-7cycloalkyl, and 5- to 14-membered heterocycloalkyl.
- R 10a is chosen from F, Cl, Br, and CH 3 .
- R 10a is F.
- R 10b is chosen from F, Cl, Br, and CH 3 .
- R 10b is Cl.
- Also provided herein is a compound of structural Formula (VI):
- V 4 is chosen from CH and N;
- R 1 is chosen from CN, halo, hydroxy, alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, (cycloalkyl)alkyl, (heterocycloalkyl)alkyl, (aryl)alkyl, and (heteroaryl)alkyl, any one of which is optionally substituted with one or more R 6 ;
- R 2 is chosen from H, halo, cyano, alkyl, (alkyl)oxy, (alkyl)thio, (alkyl)sulfonimidoyl, (alkyl)sulfonyl, cycloalkyl, and (cycloalkyl)oxy, any one of which is optionally substituted with one or more R 7 ; each R 6 and R 7 is independently chosen from CN, halo, hydroxy, NH 2 , oxo, alkyl,
- V 4 is chosen from CH and N
- R 1 is chosen from CN, halo, hydroxy, alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, (cycloalkyl)alkyl, (heterocycloalkyl)alkyl, (aryl)alkyl, and (heteroaryl)alkyl, any one of which is optionally substituted with one or more R 6
- R 2 is chosen from H, halo, cyano, alkyl, (alkyl)oxy, (alkyl)thio, (alkyl)sulfonimidoyl, (alkyl)sulfonyl, cycloalkyl, and (cycloalkyl)oxy, any one of which is optionally substituted with one or more R 7
- each R 6 and R 7 is independently chosen from CN, halo, hydroxy, alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl,
- R 10h and R 10j are H.
- R 10h is H.
- R 10h is chosen from F, Cl, and CN.
- R 10h is chosen from H, F, and Cl.
- R 10j is H.
- R 10j is H or is chosen from C 1-6 alkyl, C 3-7 cycloalkyl, 5- to 10-membered heterocycloalkyl, C6-10aryl, 5- to 7-membered heteroaryl, (C3-7cycloalkyl)CH 2 , (5- to 10-membered heterocycloalkyl)CH 2 , (C6-10aryl)CH 2 , (5- to 7-membered heteroaryl)CH 2 , (C1-6alkyl)SO 2 , (C3-7cycloalkyl)SO 2 , (5- to 10-membered heterocycloalkyl)SO 2 , (C6-10aryl)SO 2 , (5- to 7-membered heteroaryl)SO 2 , (C1-6alkyl)NH, (C3- 7cycloalkyl)NH, (5- to 10-membered heterocycloalkyl)NH, (C6-10aryl)NH, (5- to 7-membered heteroaryl)NH,
- each R 11 is independently chosen from CN, halo, hydroxy, oxo, C 1-6 alkyl, C 3- 7cycloalkyl, 4- to 11-membered heterocycloalkyl, C1-6alkylsulfonyl, haloC1- 6alkylsulfonyl, C 6-10 aryl, 5- to 14-membered heteroaryl, (C 1-6 alkyl)oxy, (C 3- 7 cycloalkyl)oxy, (4- to 11-membered heterocycloalkyl)oxy, (C 1- 6 alkylsulfonyl)oxy, (halo C 1-6 alkylsulfonyl)oxy, (C 6-10 aryl)oxy, (5- to 14- membered heteroaryl)oxy, (C1-6alkyl)NH, (C3-7cycloalkyl)NH, (4- to 11- membered heterocycloalkyl)NH, (C 1-6 alkylsulfon
- each R 11 is independently chosen from CN, halo, hydroxy, oxo, C1-6alkyl, C3- 7cycloalkyl, 4- to 11-membered heterocycloalkyl, C 1-6 alkylsulfonyl, haloC 1- 6alkylsulfonyl, C6-10aryl, 5- to 14-membered heteroaryl, (C1-6alkyl)oxy, (C3- 7cycloalkyl)oxy, (4- to 11-membered heterocycloalkyl)oxy, (C1- 6alkylsulfonyl)oxy, (halo C1-6alkylsulfonyl)oxy, (C6-10aryl)oxy, (5- to 14- membered heteroaryl)oxy, (C1-6alkyl)NH, (C3-7cycloalkyl)NH, (4- to 11- membered heterocycloalkyl)NH, (C1-6alkylsulfonyl)NH—
- each R 11 is independently chosen from C 1-6 alkyl, C 3-7 cycloalkyl, 4- to 11-membered heterocycloalkyl, C1-6alkylsulfonyl, haloC1-6alkylsulfonyl, C6-10aryl, 5- to 14- membered heteroaryl, (C 1-6 alkyl)oxy, (C 3-7 cycloalkyl)oxy, (4- to 11-membered heterocycloalkyl)oxy, (C1-6alkylsulfonyl)oxy, (halo C1-6alkylsulfonyl)oxy, (C6- 1 0 aryl)oxy, and (5- to 14-membered heteroaryl)oxy, any one of which is optionally substituted with one or two R 12 , and two R 11 can combine to form a C 5-7 cycloalkyl or 5- to 7-membered heterocycloalkyl.
- each R 11 is independently chosen from C1-6alkyl, C3-7cycloalkyl, 4- to 11-membered heterocycloalkyl, C 1-6 alkylsulfonyl, haloC 1-6 alkylsulfonyl, C 6-10 aryl, 5- to 14- membered heteroaryl, (C1-6alkyl)oxy, (C3-7cycloalkyl)oxy, (4- to 11-membered heterocycloalkyl)oxy, (C 1-6 alkylsulfonyl)oxy, (halo C 1-6 alkylsulfonyl)oxy, (C 6- 10aryl)oxy, and (5- to 14-membered heteroaryl)oxy, any one of which is optionally substituted with one or two R 12 .
- each R 11 is independently chosen from C 1-6 alkyl, C 3-7 cycloalkyl, 4- to 11-membered heterocycloalkyl, C 1-6 alkylsulfonyl, haloC 1-6 alkylsulfonyl, C 6-10 aryl, and 5- to 14- membered heteroaryl, any one of which is optionally substituted with one or two R 12 , and two R 11 can combine to form a C 5-7 cycloalkyl or 5- to 7-membered heterocycloalkyl.
- each R 11 is independently chosen from C1-6alkyl, C3-7cycloalkyl, 4- to 11-membered heterocycloalkyl, C 1-6 alkylsulfonyl, haloC 1-6 alkylsulfonyl, C 6-10 aryl, and 5- to 14- membered heteroaryl, any one of which is optionally substituted with one or two R 12 .
- each R 11 is independently chosen from C1-6alkyl, C3-7cycloalkyl, 4- to 11-membered heterocycloalkyl, C6-10aryl, and 5- to 14-membered heteroaryl, any one of which is optionally substituted with one or two R 12 , and two R 11 can combine to form a C 5-7 cycloalkyl or 5- to 7-membered heterocycloalkyl.
- each R 11 is independently chosen from C 1-6 alkyl, C 3-7 cycloalkyl, 4- to 11-membered heterocycloalkyl, C6-10aryl, and 5- to 14-membered heteroaryl, any one of which is optionally substituted with one or two R 12 .
- two R 11 when attached directly to the same carbon atom, can combine to form a C 5-7 cycloalkyl or 5- to 7-membered heterocycloalkyl. can combine to form a 5- to 7-membered heterocycloalkyl having heteroatoms selected from N, O, and S.
- two R 11 when attached directly to the same carbon atom, can combine to form a 5- to 7-membered heterocycloalkyl having 1 or 2 heteroatoms selected from N, O, and S. In certain embodiments, two R 11 , when attached directly to the same carbon atom, can combine to form a 5- to 7-membered heterocycloalkyl having 1 heteroatom selected from N, O, and S. In certain embodiments, two R 11 , when attached directly to the same carbon atom, can combine to form a 5- to 7-membered heterocycloalkyl having 1 heteroatom selected from N and O.
- two R 11 can combine to form a 5- to 7-membered heterocycloalkyl having heteroatoms selected from N, O, and S. In certain embodiments, two R 11 can combine to form a 5- to 7-membered heterocycloalkyl having 1 or 2 heteroatoms selected from N, O, and S. In certain embodiments, two R 11 can combine to form a 5- to 7- membered heterocycloalkyl having 1 heteroatom selected from N, O, and S. In certain embodiments, two R 11 can combine to form a 5- to 7-membered heterocycloalkyl having 1 heteroatom selected from N and O.
- two R 11 can combine to form a 5- to 7-membered heterocycloalkyl chosen from piperidine, pyrrolidine, tetrahydrofuran, and tetrahydro-2H-pyran.
- each R 11 is optionally substituted with one R 12 .
- R 11 is substituted with one R 12 .
- each R 12 is chosen from CN, halo, hydroxy, C1-6alkyl, (C 1-6 alkyl)oxy, and oxo.
- each R 12 is chosen from CN, halo, hydroxy, and oxo.
- each R 12 is chosen from CN and halo.
- each R 11 is unsubstituted with an R 12 .
- each R 11 is independently chosen from CN, halo, hydroxy, and oxo. In certain embodiments, each R 11 is independently chosen from CN and halo.
- R 1 is chosen from C1-6alkyl, C3-7cycloalkyl, 4- to 11- membered heterocycloalkyl, C6-14aryl, 5- to 14-membered heteroaryl, (C3-7cycloalkyl)C1- 6 alkyl, (4- to 11-membered heterocycloalkyl)C 1-6 alkyl, (C 6-14 aryl)C 1-6 alkyl, and (5- to 14- membered heteroaryl)C1-6alkyl, any one of which is optionally substituted with one or more R 6 .
- R 1 is chosen from C1-6alkyl, C3-7cycloalkyl, 4- to 11- membered heterocycloalkyl, C 6-14 aryl, 5- to 14-membered heteroaryl, (C 3-7 cycloalkyl)methyl, (4- to 11-membered heterocycloalkyl)methyl, (C6-14aryl)methyl, and (5- to 14-membered heteroaryl)methyl, any one of which is optionally substituted with one or more R 6 .
- R 1 is chosen from C1-6alkyl, C3-7cycloalkyl, 4- to 11- membered heterocycloalkyl, C 6-14 aryl, and 5- to 14-membered heteroaryl, any one of which is optionally substituted with one or more R 6 .
- R 1 is chosen from C1-6alkyl, C3-7cycloalkyl, 4- to 7- membered heterocycloalkyl, phenyl, and 5- or 6-membered heteroaryl, any one of which is optionally substituted with one or more R 6 .
- R 1 is chosen from phenyl, pyridyl, pyridinyl, pyrazinyl, pyrimidinyl, and pyridazinyl, and is optionally substituted with one or more R 6 .
- R 1 is optionally substituted with one or two R 6 .
- R 1 is optionally substituted with one R 6 .
- R 1 is substituted with one R 6 .
- R 1 is chosen from: [0135] In certain embodiments: [0136] In certain embodiments: R 1 is chosen from: [0137] In certain embodiments, R 1 is unsubstituted with an R 6 . [0138] In certain embodiments, each R 6 is independently chosen from CN, halo, hydroxy, oxo, C1-6alkyl, and (C1-6alkyl)oxy. In certain embodiments, each R 6 is independently chosen from CN, F, Cl, Br, hydroxy, and CH 3 . In certain embodiments, each R 6 is independently chosen from F, Cl, and CH 3 . In certain embodiments, each R 6 is independently chosen from F and CH 3 .
- R 2 and R 3 are independently chosen from H, halo, cyano, alkyl, (alkyl)oxy, cycloalkyl, and (cycloalkyl)oxy, any one of which is optionally substituted with one or more R 7 .
- R 2 and R 3 are independently chosen from H, halo, cyano, alkyl, (alkyl)oxy, cycloalkyl, and (cycloalkyl)oxy, any one of which is optionally substituted with one or more R 7 .
- R 2 is chosen from alkyl, (alkyl)oxy, cycloalkyl, and (cycloalkyl)oxy, any one of which is optionally substituted with one or more R 7 .
- R 2 is chosen from alkyl and cycloalkyl either one of which is optionally substituted with one or more R 7 .
- R 2 is chosen from H, halo, cyclopropyl, CH 3 , CD3,and cyano.
- R 2 is chosen from Cl, CH 3 , and CD3.
- R 2 is chosen from Cl and CH 3 .
- R 3 is chosen from alkyl, (alkyl)oxy, cycloalkyl, and (cycloalkyl)oxy, any one of which is optionally substituted with one or more R 7 .
- R 3 is chosen from H, halo, and cyano.
- R 3 is H.
- each R 7 is independently chosen from CN, halo, hydroxy, oxo, C 1-6 alkyl, and (C 1-6 alkyl)oxy.
- each R 7 is independently chosen from CN, halo, and hydroxy.
- R 2 and R 3 together with the intervening two carbons, combine to form a 5-7 membered cycloalkyl, heterocycloalkyl, aryl, or heteroaryl ring, any one of which is optionally substituted with one or more R 8 and optionally fused with a 6- membered aryl or heteroaryl ring, said 6-membered aryl or heteroaryl ring being optionally substituted with one or more R 9 .
- R 2 and R 3 together with the intervening two carbons, combine to form a 5-7 membered cycloalkyl, heterocycloalkyl, aryl, or heteroaryl ring, any one of which is optionally substituted with one or two R 8 and is fused with a 6-membered aryl or heteroaryl ring, said 6-membered aryl or heteroaryl ring being optionally substituted with one or two R 9 .
- R 2 and R 3 together with the intervening two carbons, combine to form a 5-7 membered cycloalkyl, heterocycloalkyl, aryl, or heteroaryl ring, any one of which is optionally substituted with one R 8 and is fused with a 6-membered aryl or heteroaryl ring, said 6-membered aryl or heteroaryl ring being optionally substituted with one or two R 9 .
- R 2 and R 3 together with the intervening two carbons, combine to form a 5-7 membered cycloalkyl, heterocycloalkyl, aryl, or heteroaryl ring, any one of which is unsubstituted with an R 8 and is fused with a 6- membered aryl or heteroaryl ring, said 6-membered aryl or heteroaryl ring being optionally substituted with one or two R 9 .
- R 2 and R 3 together with the intervening two carbons, combine to form a 5-7 membered cycloalkyl, heterocycloalkyl, aryl, or heteroaryl ring, any one of which is optionally substituted with one or two R 8 .
- R 2 and R 3 together with the intervening two carbons, combine to form a 5-7 membered cycloalkyl, heterocycloalkyl, aryl, or heteroaryl ring, any one of which is optionally substituted with one R 8 .
- R 2 and R 3 together with the intervening two carbons, combine to form a 5-7 membered cycloalkyl, heterocycloalkyl, aryl, or heteroaryl ring, any one of which is unsubstituted with an R 8 .
- each R 9 is independently chosen from CN, halo, hydroxy, oxo, C1-6alkyl, and (C1-6alkyl)oxy.
- each R 9 is independently chosen from CN, halo, and hydroxy.
- each R 8 is independently chosen from CN, halo, hydroxy, oxo, C1-6alkyl, and (C1-6alkyl)oxy.
- each R 8 is independently chosen from CN, halo, and hydroxy.
- any embodiment above may be combined with any one or more of these embodiments, provided the combination is not mutually exclusive.
- two embodiments are “mutually exclusive” when one is defined to be something which is different than the other. For example, an embodiment wherein two groups combine to form a cycloalkyl is mutually exclusive with an embodiment in which one group is ethyl the other group is hydrogen. Similarly, an embodiment wherein one group is CH 2 is mutually exclusive with an embodiment wherein the same group is NH.
- a compound chosen from the Examples disclosed herein, or a salt or tautomer thereof are also provided.
- Also provided are methods of inhibiting at least one RIPK1 function comprising the step of contacting RIPK1 with a compound as described herein, or a salt or tautomer thereof.
- the cell phenotype, cell proliferation, activity of RIPK1, change in biochemical output produced by active RIPK1, expression of RIPK1, or binding of RIPK1 with a natural binding partner may be monitored.
- Such methods may be modes of treatment of disease, biological assays, cellular assays, biochemical assays, or the like.
- Also provided herein are methods of treatment of a RIPK1-mediated disease comprising the administration of a therapeutically effective amount of a compound as disclosed herein, or a salt or tautomer thereof, to a patient in need thereof.
- methods of treatment of an inflammatory component of an RIPK1-mediated disease comprising the administration of a therapeutically effective amount of a compound as disclosed herein, or a salt or tautomer thereof, to a patient in need thereof.
- methods of treatment of an inflammatory component of an RIPK1-mediated disease comprising the administration of a therapeutically effective amount of a compound as disclosed herein, or a salt or tautomer thereof, to a patient in need thereof.
- methods of treatment of an inflammatory component of an RIPK1-mediated disease comprising the administration of a therapeutically effective amount of a compound as disclosed herein, or a salt or tautomer thereof, to a patient in need thereof.
- methods of treatment of an inflammatory component of an RIPK1-mediated disease comprising the administration
- the cancer is treated by promoting an appropriate immune response to the tumor.
- the appropriate immune response to the tumor comprises, or results in, one or more of the following: [0158] - an increase in the number or activity, or degree of tumor infiltration, of cytotoxic T-lymphocytes and/or natural killer cells; [0159] - an increase in the number or activity of M1 macrophages in the tumor microenvironment and/or a decrease in the in the number or activity of M2 macrophages in the tumor microenvironment; [0160] - a decrease in the number or activity of regulatory T cells; and [0161] - a decrease in the number or activity of myeloid-derived suppressor cells.
- the disease is a myelodysplastic syndrome (MDS).
- MDS myelodysplastic syndrome
- the myelodysplastic syndrome is chosen from myelodysplastic syndrome with unilineage dysplasia, myelodysplastic syndrome with multilineage dysplasia, myelodysplastic syndrome with ring sideroblasts, myelodysplastic syndrome associated with isolated del chromosome abnormality, myelodysplastic syndrome with excess blasts – type 1, and myelodysplastic syndrome with excess blasts – type 2.
- the myelodysplastic syndrome is unclassifiable myelodysplastic syndrome.
- the disease is acute myeloid leukemia (AML).
- a compound as disclosed herein, or a salt or tautomer thereof for use as a medicament.
- a compound as disclosed herein, or a salt or tautomer thereof for use as a medicament for the treatment of a RIPK1-mediated disease.
- a compound as disclosed herein, or a salt or tautomer thereof for use as a medicament for the treatment of a RIPK1-mediated disease.
- a compound as disclosed herein, or a salt or tautomer thereof as a medicament.
- a compound as disclosed herein, or a salt or tautomer thereof as a medicament for the treatment of a RIPK1-mediated disease.
- a compound as disclosed herein, or a salt or tautomer thereof for use in the manufacture of a medicament for the treatment of a RIPK1-mediated disease.
- a compound as disclosed herein, or a salt or tautomer thereof for use in the manufacture of a medicament for the treatment of a RIPK1-mediated disease.
- the use of a compound as disclosed herein, or a salt or tautomer thereof for the treatment of a RIPK1-mediated disease is also provided herein is a method of inhibition of RIPK1 comprising contacting RIPK1 with a compound as disclosed herein, or a salt or tautomer thereof.
- Also provided herein is a method for achieving an effect in a patient comprising the administration of a therapeutically effective amount of a compound as disclosed herein, or a salt or tautomer thereof, to a patient wherein the effect is chosen from cognition enhancement.
- a method of modulation of a RIPK1-mediated function in a subject comprising the administration of a therapeutically effective amount of a compound as disclosed herein, or a salt or tautomer thereof.
- a pharmaceutical composition comprising a compound as disclosed herein, or a salt or tautomer thereof, together with a pharmaceutically acceptable carrier.
- the pharmaceutical composition is formulated for oral administration.
- the oral pharmaceutical composition is chosen from a tablet and a capsule.
- a method for the synthesis of a compound of Formula (I) or a salt or tautomer thereof comprising the step of contacting an acid of formula (I-A) (I-A) with a base of formula (I-B) (I-A) in the presence of an amide coupling agent, wherein: W is chosen from CH, CR 5 , and N; R 1 is chosen from CN, halo, hydroxy, alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, (cycloalkyl)alkyl, (heterocycloalkyl)alkyl, (aryl)alkyl, and (heteroaryl)alkyl, any one of which is optionally substituted with one or more R 6 ; R 2 and R 3 are independently chosen from H, halo, cyano, alkyl, (alkyl)oxy
- the amide coupling agent is chosen from T3P and HATU.
- the reaction is performed in the presence of an amine base.
- the amine base is chosen from Et3N and iPr2NEt. Definitions [0179] As used herein, the terms below have the meanings indicated. [0180] When ranges of values are disclosed, and the notation “from n1 ... to n2” or “between n1 ... and n2” is used, where n1 and n2 are the numbers, then unless otherwise specified, this notation is intended to include the numbers themselves and the range between them. This range may be integral or continuous between and including the end values.
- the range “from 2 to 6 carbons” is intended to include two, three, four, five, and six carbons, since carbons come in integer units. Compare, by way of example, the range “from 1 to 3 ⁇ M (micromolar),” which is intended to include 1 ⁇ M, 3 ⁇ M, and everything in between to any number of significant figures (e.g., 1.255 ⁇ M, 2.1 ⁇ M, 2.9999 ⁇ M, etc.). [0181] The term “about,” as used herein, is intended to qualify the numerical values which it modifies, denoting such a value as variable within a margin of error.
- acyl refers to a carbonyl attached to an alkenyl, alkyl, aryl, cycloalkyl, heteroaryl, heterocycle, or any other moiety were the atom attached to the carbonyl is carbon.
- An “acetyl” group refers to a –C(O)CH 3 group.
- alkylcarbonyl or “alkanoyl” group refers to an alkyl group attached to the parent molecular moiety through a carbonyl group. Examples of such groups include methylcarbonyl and ethylcarbonyl. Examples of acyl groups include formyl, alkanoyl and aroyl.
- alkenyl refers to a straight- chain or branched-chain hydrocarbon radical having one or more double bonds and containing from 2 to 20 carbon atoms. In certain embodiments, said alkenyl will comprise from 2 to 6 carbon atoms.
- suitable alkenyl radicals include ethenyl, propenyl, 2-methylpropenyl, 1,4-butadienyl and the like.
- alkenyl may include “alkenylene” groups.
- alkoxy and, interchangeably, “(alkyl)oxy”, as used herein, alone or in combination, refers to an alkyl ether radical wherein the term alkyl is as defined below.
- alkyl ether radicals examples include methoxy, ethoxy, n-propoxy, isopropoxy, n- butoxy, iso-butoxy, sec-butoxy, tert-butoxy, and the like.
- alkyl refers to a straight- chain or branched-chain alkyl radical containing from 1 to 20 carbon atoms. In certain embodiments, said alkyl will comprise from 1 to 10 carbon atoms. In certain embodiments, said alkyl will comprise from 1 to 8 carbon atoms. Alkyl groups are optionally substituted as defined herein.
- alkyl radicals include methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, pentyl, iso-amyl, hexyl, octyl, noyl and the like.
- alkylene refers to a straight chain saturated hydrocarbon attached at two or more positions, such as methylene (-CH 2 -), ethylene (- CH 2 CH 2 -), and propylene (-CH 2 CH 2 CH 2 -). “Alkylene” can thus be described as –(CH 2 )n- with n being an positive integer.
- n is chosen from 1 to 20. In some embodiments, n is chosen from 1 to 10. In some embodiments, n is chosen from 1 to 8. In some embodiments, n is chosen from 1 to 6.
- alkyl may include “alkylene” groups.
- alkylamino refers to an alkyl group attached to the parent molecular moiety through an amino group. Suitable alkylamino groups may be mono- or dialkylated, forming groups such as, for example, N-methylamino, N-ethylamino, N,N-dimethylamino, N,N-ethylmethylamino and the like.
- alkylthio refers to an alkyl thioether (R–S–) radical wherein the term alkyl is as defined above and wherein the sulfur may be singly or doubly oxidized.
- suitable alkyl thioether radicals include methylthio, ethylthio, n-propylthio, isopropylthio, n-butylthio, iso-butylthio, sec-butylthio, tert-butylthio, methanesulfonyl, ethanesulfinyl, and the like.
- alkynyl refers to a straight- chain or branched chain hydrocarbon radical having one or more triple bonds and containing from 2 to 20 carbon atoms. In certain embodiments, said alkynyl comprises from 2 to 6 carbon atoms. In certain embodiments, said alkynyl comprises from 2 to 4 carbon atoms.
- alkynylene refers to a carbon-carbon triple bond attached at two positions such as ethynylene (-C:::C-, -C ⁇ C-).
- alkynyl radicals include ethynyl, propynyl, hydroxypropynyl, butyn-1- yl, butyn-2-yl, pentyn-1-yl, 3-methylbutyn-1-yl, hexyn-2-yl, and the like.
- alkynyl may include “alkynylene” groups.
- C-amido refers to a -C(O)N(RR’) group with R and R’ as defined herein or as defined by the specifically enumerated “R” groups designated.
- N-amido refers to a RC(O)N(R’)- group, with R and R’ as defined herein or as defined by the specifically enumerated “R” groups designated.
- acylamino as used herein, alone or in combination, embraces an acyl group attached to the parent moiety through an amino group.
- An example of an "acylamino” group is acetylamino (CH 3 C(O)NH-).
- amino refers to -NRR ’ wherein R and R ’ are independently chosen from hydrogen, alkyl, acyl, heteroalkyl, aryl, cycloalkyl, heteroaryl, and heterocycloalkyl, any of which may themselves be optionally substituted. Additionally, R and R’ may combine to form heterocycloalkyl, either of which is optionally substituted.
- aryl as used herein, alone or in combination, means a carbocyclic aromatic system containing one, two or three rings wherein such polycyclic ring systems are fused together.
- aryl embraces aromatic groups such as phenyl, naphthyl, anthracenyl, and phenanthryl.
- arylalkyl or aralkyl refers to an aryl group attached to the parent molecular moiety through an alkyl group.
- arylalkanoyl or “aralkanoyl” or “aroyl,”as used herein, alone or in combination, refers to an acyl radical derived from an aryl-substituted alkanecarboxylic acid such as benzoyl, napthoyl, phenylacetyl, 3-phenylpropionyl (hydrocinnamoyl), 4- phenylbutyryl, (2-naphthyl)acetyl, 4-chlorohydrocinnamoyl, and the like.
- aryloxy as used herein, alone or in combination, refers to an aryl group attached to the parent molecular moiety through an oxy.
- carbamate as used herein, alone or in combination, refers to an ester of carbamic acid (-NHCOO-) which may be attached to the parent molecular moiety from either the nitrogen or acid end, and which is optionally substituted as defined herein.
- -carbamyl as used herein, alone or in combination, refers to a -OC(O)NRR’, group-with R and R’ as defined herein.
- N-carbamyl refers to a ROC(O)NR’- group, with R and R’ as defined herein.
- carbonyl as used herein, when alone includes formyl [-C(O)H] and in combination is a -C(O)- group.
- carboxyl or “carboxy,” as used herein, refers to -C(O)OH or the corresponding “carboxylate” anion, such as is in a carboxylic acid salt.
- An “O-carboxy” group refers to a RC(O)O- group, where R is as defined herein.
- a “C-carboxy” group refers to a -C(O)OR groups where R is as defined herein.
- said cycloalkyl will comprise a spirocycle ring system.
- cycloalkyl groups include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, tetrahydronapthyl, indanyl, octahydronaphthyl, 2,3-dihydro-1H-indenyl, adamantyl and the like.
- “Bicyclic” and “tricyclic” as used herein are intended to include both fused ring systems, such as decahydronaphthalene, octahydronaphthalene as well as the multicyclic (multicentered) saturated or partially unsaturated type.
- the latter type of isomer is exemplified in general by, bicyclo[1.1.1]pentane, camphor, adamantane, and bicyclo[3.2.1]octane.
- the term “ester,” as used herein, alone or in combination, refers to a carboxy group bridging two moieties linked at carbon atoms.
- ether refers to an oxy group bridging two moieties linked at carbon atoms.
- halo refers to fluorine, chlorine, bromine, or iodine.
- haloalkoxy refers to a haloalkyl group attached to the parent molecular moiety through an oxygen atom.
- haloalkyl refers to an alkyl radical having the meaning as defined above wherein one or more hydrogens are replaced with a halogen.
- a monohaloalkyl radical for one example, may have an iodo, bromo, chloro or fluoro atom within the radical.
- Dihalo and polyhaloalkyl radicals may have two or more of the same halo atoms or a combination of different halo radicals.
- haloalkyl radicals include fluoromethyl, difluoromethyl, trifluoromethyl, chloromethyl, dichloromethyl, trichloromethyl, pentafluoroethyl, heptafluoropropyl, difluorochloromethyl, dichlorofluoromethyl, difluoroethyl, difluoropropyl, dichloroethyl and dichloropropyl.
- “Haloalkylene” refers to a haloalkyl group attached at two or more positions. Examples include fluoromethylene (-CFH-), difluoromethylene (-CF 2 -), chloromethylene (-CHCl-) and the like.
- heteroalkyl refers to a stable straight or branched chain, or combinations thereof, fully saturated or containing from 1 to 3 degrees of unsaturation, consisting of the stated number of carbon atoms and one, two, or three heteroatoms chosen from N, O, and S, and wherein the N and S atoms may optionally be oxidized and the N heteroatom may optionally be quaternized.
- the heteroatom(s) may be placed at any interior position of the heteroalkyl group. Up to two heteroatoms may be consecutive, such as, for example, -CH 2 -NH-OCH 3 .
- heteroaryl refers to a 3 to 15 membered unsaturated heteromonocyclic ring, or a fused monocyclic, bicyclic, or tricyclic ring system in which at least one of the fused rings is aromatic, which contains at least one atom chosen from N, O, and S.
- said heteroaryl will comprise from 1 to 4 heteroatoms as ring members.
- said heteroaryl will comprise from 1 to 2 heteroatoms as ring members.
- said heteroaryl will comprise from 5 to 7 atoms.
- heterocyclic rings are fused with aryl rings wherein heteroaryl rings are fused with other heteroaryl rings wherein heteroaryl rings are fused with heterocycloalkyl rings, or wherein heteroaryl rings are fused with cycloalkyl rings.
- heteroaryl groups include pyrrolyl, pyrrolinyl, imidazolyl, pyrazolyl, pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl, triazolyl, pyranyl, furyl, thienyl, oxazolyl, isoxazolyl, oxadiazolyl, thiazolyl, thiadiazolyl, isothiazolyl, indolyl, isoindolyl, indolizinyl, benzimidazolyl, quinolyl, isoquinolyl, quinoxalinyl, quinazolinyl, indazolyl, benzotriazolyl, benzodioxolyl, benzopyranyl, benzoxazolyl, benzoxadiazolyl, benzothiazolyl, benzothiadiazolyl, benzofuryl, benzothienyl, chromonyl,
- Exemplary tricyclic heterocyclic groups include carbazolyl, benzidolyl, phenanthrolinyl, dibenzofuranyl, acridinyl, phenanthridinyl, xanthenyl and the like.
- heterocycloalkyl and, interchangeably, “heterocycle,” as used herein, alone or in combination, each refer to a saturated, partially unsaturated, or fully unsaturated (but nonaromatic) monocyclic; saturated, partially unsaturated, or fully unsaturated (but not fully aromatic) bicyclic; or saturated, partially unsaturated, or fully unsaturated (but not fully aromatic) tricyclic heterocyclic group containing at least one heteroatom as a ring member wherein each said heteroatom may be independently chosen from nitrogen, oxygen, and sulfur.
- the term includes polycyclic groups which comprise at least one nonaromatic ring, such as 1,2-dihydroquinoline, 5,6-dihydroquinoline, and 2,3-dihydrobenzofuran.
- the term excludes polycyclic groups in which every ring is nonaromatic, such as indole, quinoline, and acridine.
- said heterocycloalkyl will comprise a spirocycle ring system.
- said hetercycloalkyl will comprise from 1 to 4 heteroatoms as ring members.
- said hetercycloalkyl will comprise from 1 to 2 heteroatoms as ring members.
- said hetercycloalkyl will comprise from 3 to 8 ring members in each ring. In certain embodiments, said hetercycloalkyl will comprise from 3 to 7 ring members in each ring. In certain embodiments, said hetercycloalkyl will comprise from 5 to 6 ring members in each ring.
- “Heterocycloalkyl” and “heterocycle” are intended to include sulfones, sulfoxides, N-oxides of tertiary nitrogen ring members, and carbocyclic fused and benzo fused ring systems; additionally, both terms also include systems where a heterocycle ring is fused to an aryl or heteroaryl group, as defined herein, or an additional heterocycle group.
- heterocycle groups include aziridinyl, azetidinyl, 1,3-benzodioxolyl, dihydroisoindolyl, dihydroisoquinolinyl, dihydrocinnolinyl, dihydrobenzodioxinyl, dihydro[1,3]oxazolo[4,5-b]pyridinyl, benzothiazolyl, dihydroindolyl, dihy-dropyridinyl, 1,3-dioxanyl, 1,4-dioxanyl, 1,3-dioxolanyl, isoindolinyl, morpholinyl, piperazinyl, pyrrolidinyl, tetrahydropyridinyl, piperidinyl, thiomorpholinyl, and the like.
- hydroxy refers to -OH.
- hydroxyalkyl refers to a hydroxy group attached to the parent molecular moiety through an alkyl group.
- linear chain of atoms refers to the longest straight chain of atoms independently chosen from carbon, nitrogen, oxygen and sulfur.
- lower means containing from 1 to and including 6 carbon atoms (i.e., C1-C6 alkyl).
- lower cycloalkyl means a monocyclic cycloalkyl having between three and six ring members (i.e., C 3 -C 6 cycloalkyl). Lower cycloalkyls may be unsaturated. Examples of lower cycloalkyl include cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl.
- lower heterocycloalkyl means a monocyclic heterocycloalkyl having between three and six ring members, of which between one and four may be heteroatoms chosen from N, O, and S (i.e., C3-C6 heterocycloalkyl).
- Examples of lower heterocycloalkyls include pyrrolidinyl, imidazolidinyl, pyrazolidinyl, piperidinyl, piperazinyl, and morpholinyl.
- Lower heterocycloalkyls may be unsaturated.
- lower amino refers to -NRR ’ wherein R and R ’ are independently chosen from hydrogen and lower alkyl, either of which is optionally substituted.
- nitro refers to –NO 2 .
- oxo refers to —O.
- perhaloalkoxy refers to an alkoxy group where all of the hydrogen atoms are replaced by halogen atoms.
- perhaloalkyl refers to an alkyl group where all of the hydrogen atoms are replaced by halogen atoms.
- spirocycle ring system refers to a polycyclic ring system comprising two rings such that a single atom is common to both rings.
- sulfonate refers to a polycyclic ring system comprising two rings such that a single atom is common to both rings.
- sulfonate “sulfonic acid,” and “sulfonic,” as used herein, alone or in combination, refer the –SO 3 H group and its anion as the sulfonic acid is used in salt formation.
- sulfanyl as used herein, alone or in combination, refers to –S–.
- sulfinyl refers to —S(O)–.
- sulfonyl refers to —S(O)2–.
- thia and thio refer to a – S– group or an ether wherein the oxygen is replaced with sulfur.
- the oxidized derivatives of the thio group namely sulfinyl: -SO-, sulfonyl: -SO 2 -, and sulfonimidoyl: -SO(NH)-, are included in the definition of thia and thio.
- thiol refers to an —SH group.
- thiocyanato refers to a –CNS group.
- trimethysilyl tert-butyldimethylsilyl, triphenylsilyl and the like.
- Any definition herein may be used in combination with any other definition to describe a composite structural group. By convention, the trailing element of any such definition is that which attaches to the parent moiety.
- the composite group alkylamido would represent an alkyl group attached to the parent molecule through an amido group
- the term alkoxyalkyl would represent an alkoxy group attached to the parent molecule through an alkyl group.
- the substituents of an “optionally substituted” group may include, without limitation, one or more substituents independently chosen from the following groups or a particular designated set of groups, alone or in combination: lower alkyl, lower alkenyl, lower alkynyl, lower alkanoyl, lower heteroalkyl, lower heterocycloalkyl, lower haloalkyl, lower haloalkenyl, lower haloalkynyl, lower perhaloalkyl, lower perhaloalkoxy, lower cycloalkyl, phenyl, aryl, aryloxy, lower alkoxy, lower haloalkoxy, oxo, lower acyloxy, carbonyl, carboxyl, lower alkylcarbonyl, lower carboxyester, lower carboxamido, cyano, hydrogen, halogen, hydroxy, amino, lower alkylamino, arylamino, amido, nitro, thiol, lower alkylthio, lower hal
- two substituents may be joined together to form a fused five-, six-, or seven- membered carbocyclic or heterocyclic ring consisting of zero to three heteroatoms, for example forming methylenedioxy or ethylenedioxy.
- An optionally substituted group may be unsubstituted (e.g., -CH 2 CH 3 ), fully substituted (e.g., -CF2CF3), monosubstituted (e.g., - CH 2 CH 2 F) or substituted at a level anywhere in-between fully substituted and monosubstituted (e.g., -CH 2 CF3).
- R or the term R’ appearing by itself and without a number designation, unless otherwise defined, refers to a moiety chosen from hydrogen, alkyl, cycloalkyl, heteroalkyl, aryl, heteroaryl and heterocycloalkyl, any of which is optionally substituted.
- an unsymmetrical group such as -C(O)N(R)- may be attached to the parent moiety at either the carbon or the nitrogen.
- Asymmetric centers exist in the compounds, salts, and tautomers disclosed herein. These centers are designated by the symbols “R” or “S,” depending on the configuration of substituents around the chiral carbon atom. It should be understood that the invention encompasses all stereochemical isomeric forms, including diastereomeric, enantiomeric, and epimeric forms,as well as d-isomers and 1-isomers, and mixtures thereof.
- Individual stereoisomers of compounds, salts, and tautomers can be prepared synthetically from commercially available starting materials which contain chiral centers or by preparation of mixtures of enantiomeric products followed by separation such as conversion to a mixture of diastereomers followed by separation or recrystallization, chromatographic techniques, direct separation of enantiomers on chiral chromatographic columns, or any other appropriate method known in the art.
- Starting compounds, salts, and tautomers of particular stereochemistry are either commercially available or can be made and resolved by techniques known in the art. Additionally, the compounds, salts, and tautomers disclosed herein may exist as geometric isomers.
- the present invention includes all cis, trans, syn, anti,
- E
- Z
- the term “tautomers”, as used herein, alone or in combination, refers to a pair of compounds which differ in the attachment of a hydrogen and disposition of a double bond, and which rapidly interconvert in conventional media. Tautomeric pairs that are recognized to the person of skill include, but are not limited to, keto / enol tautomers, 2-hydroxypyridine / 2-pyridone tautomers, lactam / lactim tautomers, and imine / enamine tautomers.
- a dashed line between two atoms in a drawing of a molecule indicates that an additional bond may be present or absent at that position.
- Disease as used herein is intended to be generally synonymous, and is used interchangeably with, the terms “disorder,” “syndrome,” and “condition” (as in medical condition), in that all reflect an abnormal condition of the human or animal body or of one of its parts that impairs normal functioning, is typically manifested by distinguishing signs and symptoms, and causes the human or animal to have a reduced duration or quality of life.
- combination therapy means the administration of two or more therapeutic agents to treat a therapeutic condition or disorder described in the present disclosure.
- RIPK1 binder is used herein to refer to a compound, or a salt or tautomer thereof, that exhibits an K d with respect to RIPK1 of no more than about 100 ⁇ M and more typically not more than about 50 ⁇ M, as measured in the RIPK1 binding assay described generally herein.
- the RIPK1 binding assay measures the K d (dissociation constant) for the binding of a compound, or a salt or tautomer thereof with the active site of RIPK1. Certain compounds disclosed herein, or a salt or tautomer thereof, have been discovered to bind to RIPK1.
- compounds, or salts or tautomers thereof will exhibit an K d with respect to RIPK1 of no more than about 10 ⁇ M; in certain embodiments, compounds, or salts or tautomers thereof, will exhibit a K d with respect to RIPK1 of no more than about 1 ⁇ M; in certain embodiments, compounds, or salts or tautomers thereof, will exhibit a Kd with respect to RIPK1 of not more than about 0.1 ⁇ M; in certain embodiments, compounds, or salts or tautome thereof, will exhibit a Kd with respect to RIPK1 of not more than about 10 nM, as measured in the RIPK1 assay described herein.
- the phrase "therapeutically effective” is intended to qualify the amount of active ingredients used in the treatment of a disease or disorder or on the effecting of a clinical endpoint.
- the term “therapeutically acceptable” refers to those compounds (or salts, or tautomers thereof) which are suitable for use in contact with the tissues of patients without undue toxicity, irritation, and allergic response, are commensurate with a reasonable benefit / risk ratio, and are effective for their intended use.
- treatment As used herein, reference to "treatment” of a patient is intended to include prophylaxis. Treatment may also be preemptive in nature, i.e., it may include prevention of disease.
- Prevention of a disease may involve complete protection from disease, for example as in the case of prevention of infection with a pathogen, or may involve prevention of disease progression.
- prevention of a disease may not mean complete foreclosure of any effect related to the diseases at any level, but instead may mean prevention of the symptoms of a disease to a clinically significant or detectable level.
- Prevention of diseases may also mean prevention of progression of a disease to a later stage of the disease.
- the term “patient” is generally synonymous with the term “subject” and includes all mammals including humans. Examples of patients include humans, livestock such as cows, goats, sheep, pigs, and rabbits, and companion animals such as dogs, cats, rabbits, and horses. Preferably, the patient is a human.
- the compounds disclosed herein can exist as therapeutically acceptable salts.
- the present invention includes compounds listed above, and tautomers thereof, in the form of salts, including acid addition salts.
- Suitable salts include those formed with both organic and inorganic acids. Such acid addition salts will normally be pharmaceutically acceptable. However, salts of non-pharmaceutically acceptable salts may be of utility in the preparation and purification of the compound in question. Basic addition salts may also be formed and be pharmaceutically acceptable.
- Pharmaceutical Salts Properties, Selection, and Use (Stahl, P. Heinrich. Wiley-VCHA, Zurich, Switzerland, 2002).
- terapéuticaally acceptable salt represents salts or zwitterionic forms of the compounds disclosed herein which are water or oil-soluble or dispersible and therapeutically acceptable as defined herein.
- the salts can be prepared during the final isolation and purification of the compounds or separately by reacting the appropriate compound in the form of the free base with a suitable acid.
- Representative acid addition salts include acetate, adipate, alginate, L-ascorbate, aspartate, benzoate, benzenesulfonate (besylate), bisulfate, butyrate, camphorate, camphorsulfonate, citrate, digluconate, formate, fumarate, gentisate, glutarate, glycerophosphate, glycolate, hemisulfate, heptanoate, hexanoate, hippurate, hydrochloride, hydrobromide, hydroiodide, 2-hydroxyethansulfonate (isethionate), lactate, maleate, malonate, DL-mandelate, mesitylenesulfonate, methanesulfonate, naphthylenesulfonate, nicotinate, 2-naphthalenesulfonate, oxalate, pamoate, pectinate, persulfate, 3-phenyl
- basic groups in the compounds disclosed herein can be quaternized with methyl, ethyl, propyl, and butyl chlorides, bromides, and iodides; dimethyl, diethyl, dibutyl, and diamyl sulfates; decyl, lauryl, myristyl, and steryl chlorides, bromides, and iodides; and benzyl and phenethyl bromides.
- acids which can be employed to form therapeutically acceptable addition salts include inorganic acids such as hydrochloric, hydrobromic, sulfuric, and phosphoric, and organic acids such as oxalic, maleic, succinic, and citric.
- Salts can also be formed by coordination of the compounds with an alkali metal or alkaline earth ion.
- the present invention contemplates sodium, potassium, magnesium, and calcium salts of the compounds disclosed herein, and tautomers thereof, and the like.
- Basic addition salts can be prepared during the final isolation and purification of the compounds by reacting a carboxy group with a suitable base such as the hydroxide, carbonate, or bicarbonate of a metal cation or with ammonia or an organic primary, secondary, or tertiary amine.
- the cations of therapeutically acceptable salts include lithium, sodium, potassium, calcium, magnesium, and aluminum, as well as nontoxic quaternary amine cations such as ammonium, tetramethylammonium, tetraethylammonium, methylamine, dimethylamine, trimethylamine, triethylamine, diethylamine, ethylamine, tributylamine, pyridine, N,N-dimethylaniline, N-methylpiperidine, N-methylmorpholine, dicyclohexylamine, procaine, dibenzylamine, N,N-dibenzylphenethylamine, 1-ephenamine, and N,N'-dibenzylethylenediamine.
- nontoxic quaternary amine cations such as ammonium, tetramethylammonium, tetraethylammonium, methylamine, dimethylamine, trimethylamine, triethylamine, diethylamine,
- compositions which comprise one or more of certain compounds disclosed herein, or one or more pharmaceutically acceptable salts, or tautomers thereof, together with one or more pharmaceutically acceptable carriers thereof and optionally one or more other therapeutic ingredients.
- the carrier(s) must be "acceptable" in the sense of being compatible with the other ingredients of the formulation and not deleterious to the recipient thereof. Proper formulation is dependent upon the route of administration chosen.
- compositions disclosed herein may be manufactured in any manner known in the art, e.g., by means of conventional mixing, dissolving, granulating, dragee-making, levigating, emulsifying, encapsulating, entrapping or compression processes.
- formulations include those suitable for oral, parenteral (including subcutaneous, intradermal, intramuscular, intravenous, intraarticular, and intramedullary), intraperitoneal, transmucosal, transdermal, rectal and topical (including dermal, buccal, sublingual and intraocular) administration although the most suitable route may depend upon for example the condition and disorder of the recipient.
- the formulations may conveniently be presented in unit dosage form and may be prepared by any of the methods well known in the art of pharmacy. Typically, these methods include the step of bringing into association a compound, salt, or tautomer of the subject invention or a pharmaceutically acceptable salt, or tautomer thereof ("active ingredient”) with the carrier which constitutes one or more accessory ingredients.
- formulations are prepared by uniformly and intimately bringing into association the active ingredient with liquid carriers or finely divided solid carriers or both and then, if necessary, shaping the product into the desired formulation.
- Formulations of the compounds, or salts or tautomers thereof disclosed herein suitable for oral administration may be presented as discrete units such as capsules, cachets or tablets each containing a predetermined amount of the active ingredient; as a powder or granules; as a solution or a suspension in an aqueous liquid or a non-aqueous liquid; or as an oil-in-water liquid emulsion or a water-in-oil liquid emulsion.
- the active ingredient may also be presented as a bolus, electuary or paste.
- compositions which can be used orally include tablets, push-fit capsules made of gelatin, as well as soft, sealed capsules made of gelatin and a plasticizer, such as glycerol or sorbitol. Tablets may be made by compression or molding, optionally with one or more accessory ingredients. Compressed tablets may be prepared by compressing in a suitable machine the active ingredient in a free-flowing form such as a powder or granules, optionally mixed with binders, inert diluents, or lubricating, surface active or dispersing agents.
- Molded tablets may be made by molding in a suitable machine a mixture of the powdered compound, or a salt or tautomer thereof, moistened with an inert liquid diluent.
- the tablets may optionally be coated or scored and may be formulated so as to provide slow or controlled release of the active ingredient therein. All formulations for oral administration should be in dosages suitable for such administration.
- the push-fit capsules can contain the active ingredients in admixture with filler such as lactose, binders such as starches, and / or lubricants such as talc or magnesium stearate and, optionally, stabilizers.
- the active compounds, or salts or tautomers thereof may be dissolved or suspended in suitable liquids, such as fatty oils, liquid paraffin, or liquid polyethylene glycols.
- suitable liquids such as fatty oils, liquid paraffin, or liquid polyethylene glycols.
- stabilizers may be added.
- Dragee cores are provided with suitable coatings.
- suitable coatings For this purpose, concentrated sugar solutions may be used, which may optionally contain gum arabic, talc, polyvinyl pyrrolidone, carbopol gel, polyethylene glycol, and / or titanium dioxide, lacquer solutions, and suitable organic solvents or solvent mixtures.
- Dyestuffs or pigments may be added to the tablets or dragee coatings for identification or to characterize different combinations of active compound doses, or salts or tautomers thereof.
- the compounds, or a salt or tautomer thereof may be formulated for parenteral administration by injection, e.g., by bolus injection or continuous infusion.
- Formulations for injection may be presented in unit dosage form, e.g., in ampoules or in multi-dose containers, with an added preservative.
- the compositions may take such forms as suspensions, solutions or emulsions in oily or aqueous vehicles, and may contain formulatory agents such as suspending, stabilizing and / or dispersing agents.
- the formulations may be presented in unit- dose or multi-dose containers, for example sealed ampoules and vials, and may be stored in powder form or in a freeze-dried (lyophilized) condition requiring only the addition of the sterile liquid carrier, for example, saline or sterile pyrogen-free water, immediately prior to use.
- sterile liquid carrier for example, saline or sterile pyrogen-free water
- Extemporaneous injection solutions and suspensions may be prepared from sterile powders, granules and tablets of the kind previously described.
- Formulations for parenteral administration include aqueous and non-aqueous (oily) sterile injection solutions of the active compounds, or a salt or tautomer thereof, which may contain antioxidants, buffers, bacteriostats and solutes which render the formulation isotonic with the blood of the intended recipient; and aqueous and non-aqueous sterile suspensions which may include suspending agents and thickening agents.
- Suitable lipophilic solvents or vehicles include fatty oils such as sesame oil, or synthetic fatty acid esters, such as ethyl oleate or triglycerides, or liposomes.
- Aqueous injection suspensions may contain substances which increase the viscosity of the suspension, such as sodium carboxymethyl cellulose, sorbitol, or dextran.
- the suspension may also contain suitable stabilizers or agents which increase the solubility of the compounds, or salts or tautomer thereof, to allow for the preparation of highly concentrated solutions.
- the compounds, or salts or tautomers thereof may also be formulated as a depot preparation. Such long acting formulations may be administered by implantation (for example subcutaneously or intramuscularly) or by intramuscular injection.
- the compounds, or salts or tautomers thereof may be formulated with suitable polymeric or hydrophobic materials (for example as an emulsion in an acceptable oil) or ion exchange resins, or as sparingly soluble derivatives, for example, as a sparingly soluble salt.
- suitable polymeric or hydrophobic materials for example as an emulsion in an acceptable oil
- ion exchange resins for example, as an emulsion in an acceptable oil
- sparingly soluble derivatives for example, as a sparingly soluble salt.
- the compositions may take the form of tablets, lozenges, pastilles, or gels formulated in conventional manner. Such compositions may comprise the active ingredient in a flavored basis such as sucrose and acacia or tragacanth.
- the compounds, or salts or tautomers thereof may also be formulated in rectal compositions such as suppositories or retention enemas, e.g., containing conventional suppository bases such as cocoa butter, polyethylene glycol, or other glycerides.
- rectal compositions such as suppositories or retention enemas, e.g., containing conventional suppository bases such as cocoa butter, polyethylene glycol, or other glycerides.
- Certain compounds, or salts or tautomers thereof, disclosed herein may be administered topically, that is by non-systemic administration.
- compositions suitable for topical administration include liquid or semi-liquid preparations suitable for penetration through the skin to the site of inflammation such as gels, liniments, lotions, creams, ointments or pastes, and drops suitable for administration to the eye, ear or nose.
- the active ingredient for topical administration may comprise, for example, from 0.001% to 10% w / w (by weight) of the formulation. In certain embodiments, the active ingredient may comprise as much as 10% w / w. In other embodiments, it may comprise less than 5% w / w. In certain embodiments, the active ingredient may comprise from 2% w / w to 5% w / w. In other embodiments, it may comprise from 0.1% to 1% w / w of the formulation. [0266] For administration by inhalation, compounds, or salts or tautomers thereof, may be conveniently delivered from an insufflator, nebulizer pressurized packs or other convenient means of delivering an aerosol spray.
- Pressurized packs may comprise a suitable propellant such as dichlorodifluoromethane, trichlorofluoromethane, dichlorotetrafluoroethane, carbon dioxide or other suitable gas.
- a suitable propellant such as dichlorodifluoromethane, trichlorofluoromethane, dichlorotetrafluoroethane, carbon dioxide or other suitable gas.
- the dosage unit may be determined by providing a valve to deliver a metered amount.
- the compounds, salts, and tautomers according to the invention may take the form of a dry powder composition, for example a powder mix of the compound, or salt or tautomer thereof, and a suitable powder base such as lactose or starch.
- the powder composition may be presented in unit dosage form, in for example, capsules, cartridges, gelatin or blister packs from which the powder may be administered with the aid of an inhalator or insufflator.
- Preferred unit dosage formulations are those containing an effective dose, as herein below recited, or an appropriate fraction thereof, of the active ingredient.
- the formulations described above may include other agents conventional in the art having regard to the type of formulation in question, for example those suitable for oral administration may include flavoring agents.
- Administration and Treatment Compounds, or salts or tautomers thereof, may be administered orally or via injection at a dose of from 0.1 to 500 mg / kg per day.
- the dose range for adult humans is generally from 5 mg to 2 g / day. Tablets or other forms of presentation provided in discrete units may conveniently contain an amount of one or more compounds, or salts or tautomers thereof, which is effective at such dosage or as a multiple of the same, for instance, units containing 5 mg to 500 mg, usually around 10 mg to 200 mg.
- the amount of active ingredient that may be combined with the carrier materials to produce a single dosage form will vary depending upon the host treated and the particular mode of administration.
- the compounds, or salts or tautomers thereof can be administered in various modes, e.g. orally, topically, or by injection.
- the precise amount of compound, or salt or tautomer thereof, administered to a patient will be the responsibility of the attendant physician.
- the specific dose level for any particular patient will depend upon a variety of factors including the activity of the specific compound employed, or salt or tautomer thereof, the age, body weight, general health, sex, diets, time of administration, route of administration, rate of excretion, drug combination, the precise disorder being treated, and the severity of the indication or condition being treated. Also, the route of administration may vary depending on the condition and its severity. [0272] In certain instances, it may be appropriate to administer at least one of the compounds described herein (or a pharmaceutically acceptable salt, or tautomer thereof) in combination with another therapeutic agent.
- one of the side effects experienced by a patient upon receiving one of the compounds herein, or salt or tautomer thereof, is hypertension
- the therapeutic effectiveness of one of the compounds described herein, or salts or tautomers thereof may be enhanced by administration of an adjuvant (i.e., by itself the adjuvant may only have minimal therapeutic benefit, but in combination with another therapeutic agent, the overall therapeutic benefit to the patient is enhanced).
- the benefit of experienced by a patient may be increased by administering one of the compounds described herein, or salts or tautomers thereof, with another therapeutic agent (which also includes a therapeutic regimen) that also has therapeutic benefit.
- another therapeutic agent which also includes a therapeutic regimen
- increased therapeutic benefit may result by also providing the patient with another therapeutic agent for diabetes.
- the overall benefit experienced by the patient may simply be additive of the two therapeutic agents or the patient may experience a synergistic benefit.
- Specific, non-limiting examples of possible combination therapies include use of certain compounds, salts, and tautomers of the invention with: donepezil, rivastigmine, galantamine, and memantine. Further examples include anti-amyloid antibodies and vaccines, anti-Ab antibodies and vaccines, anti-tau antibodies and vaccines, ⁇ -secretase inhibitors, 5- HT4 agonists, 5-HT6 antagonists, 5-HT1a antagonists, ⁇ 7 nicotinic receptor agonists, 5-HT3 receptor antagonists, PDE4 inhibitors, O-glycnacase inhibitors, and other medicines approved for the treatment of Alzheimer’s disease.
- the multiple therapeutic agents may be administered in any order or even simultaneously. If simultaneously, the multiple therapeutic agents may be provided in a single, unified form, or in multiple forms (by way of example only, either as a single pill or as two separate pills). One of the therapeutic agents may be given in multiple doses, or both may be given as multiple doses. If not simultaneous, the timing between the multiple doses may be any duration of time ranging from a few minutes to four weeks.
- certain embodiments provide methods for treating RIPK1-mediated disorders in a human or animal subject in need of such treatment comprising administering to said subject an amount of a compound disclosed herein, or a salt or tautomer thereof, effective to reduce or prevent said disorder in the subject, in combination with at least one additional agent for the treatment of said disorder that is known in the art.
- certain embodiments provide therapeutic compositions comprising at least one compound disclosed herein, or salt or tautomer thereof, in combination with one or more additional agents for the treatment of RIPK1-mediated disorders.
- a RIPK1 inhibitor may be optimally used together with one or more of the following non-limiting examples of anti-cancer agents: 1) inhibitors or modulators of a protein involved in one or more of the DNA damage repair (DDR) pathways such as: a. PARP1/2, including, but not limited to: olaparib, niraparib, rucaparib; b. checkpoint kinase 1 (CHK1), including, but not limited to: UCN-01, AZD7762, PF477736, SCH900776, MK-8776, LY2603618, V158411, and EXEL-9844; c.
- DDR DNA damage repair
- checkpoint kinase 2 (CHK2), including, but not limited to: PV1019, NSC 109555, and VRX0466617; d. dual CHK1 / CHK2, including, but not limited to: XL-844, AZD7762, and PF- 473336; e. WEE1, including, but not limited to: MK-1775 and PD0166285; f. ATM, including, but not limited to KU-55933, g. DNA-dependent protein kinase, including, but not limited to NU7441 and M3814; and h. Additional proteins involved in DDR; 2) Inhibitors or modulators of one or more immune checkpoints, including, but not limited to: a.
- PD-1 inhibitors such as nivolumab (OPDIVO), pembrolizumab (KEYTRUDA), pidilizumab (CT-011), and AMP-224 (AMPLIMMUNE);
- PD-L1 inhibitors such as Atezolizumab (TECENTRIQ), Avelumab (Bavencio), Durvalumab (Imfinzi), MPDL3280A (Tecentriq), BMS-936559, and MEDI4736;
- anti-CTLA-4 antibodies such as ipilimumab (YERVOY) and CP-675,206 (TREMELIMUMAB); d.
- Tim-3 T-cell immunoglobulin and mucin domain 3
- Vista V-domain Ig suppressor of T cell activation
- BTLA band T lymphocyte attenuator
- LAG3 lymphocyte activation gene 3
- T cell immunoglobulin and immunoreceptor tyrosine-based inhibitory motif domain TAGIT
- telomerase inhibitors or telomeric DNA binding compounds TAGIT
- alkylating agents including, but not limited to: chlorambucil (LEUKERAN), oxaliplatin (ELOXATIN), streptozocin (ZANOSAR), dacarbazine, ifosfamide, lomustine (CCNU), procarbazine (MATULAN), temozolomide (TEMODAR), and thiotepa
- DNA crosslinking agents including, but not limited to: carmustine, chlorambucil (LEUKERAN), carboplatin (PARAPLATIN), cisplatin (PLATIN), busulfan (MYLERAN), melphalan (ALKERAN), mitomycin (MITOSOL), and cyclophosphamide (ENDOXAN); 6) anti-metabolites, including, but not limited to: cla
- tetracyclines including, but not limited to: doxycycline; b. erythromycins, including, but not limited to: azithromycin; c. glycylglycines, including, but not limited to: tigecycline; d. antiphrastic, including, but not limited to: pyrvinium pamoate; e. beta-lactams, including, but not limited to the penicillins and cephalosporins; f. anthracycline antibiotics, including, but not limited to: daunorubicin and doxorubicin; g.
- antibody therapeutic agents including, but not limited to: muromonab-CD3, infliximab (REMICADE), adalimumab (HUMIRA), omalizumab (XOLAIR), daclizumab (ZENAPAX), rituximab (RITUXAN), ibritumomab (ZEVALIN), tositumomab (BEXXAR), cetuximab (ERBITUX), trastuzumab (HERCEPTIN), ADCETRIS, alemtuzumab (CAMPATH-1H), Lym-1 (ONCOLYM), ipilimumab (YERVOY), vitaxin, bevacizumab (AVASTIN), and abciximab (REOPRO); and 25) other agents, such as Bacillus Calmette–Guérin (B-C-G) vaccine
- An RIPK1 inhibitor may be optimally used together with one or more of the following therapeutics for myelodysplastic syndromes: 1) growth factors, such as epoetin (EPOGEN®, PROCRIT®), darbepoetin alfa (ARANESP®), luspatercept (REBLOZYL®), filgrastim (NEUPOGEN®), pegfilgrastim (NEULASTA®), romiplostim (NPLATE®), eltrombopag (PROMACTA®), and oprelvekin (NEUMEGA); 2) hypomethylating agents, such as azacitidine (ONUREG®, VIDAZA®); 3) antineoplastics, such as idarubicin (IDAMYCIN®), daunorubicin (CERUBIDINE®), [0278] An RIPK1 inhibitor may be optimally used together with one or more of the following non-limiting examples of CNS agents: 1) catecholamine agents such as L-DO
- beta blockers such as timolol
- alpha agonists such as brimonidine (ALPHAGAN®) and apraclonidine (IOPIDINE®)
- rho kinase inhibitors such as netarsudil (RHOPRESSA®, RHOKIINSA®)
- carbonic anhydrase inhibitors such as dorzolamide (TRUSOPT®), brinzolamide (AZOPT®), acetazolamide (DIAMOX®), and methazolamide (NEPTAZANE®); 6) multiple sclerosis medications, including: a.
- immunomodulators such as glatiramer (COPAXONE®), ofatumumab (KESIMPTA®), and interferon and its derivatives;
- monoclonal antibodies such as alemtuzumab (LEMTRADA®), ocrelizumab (OCREVUS®), and natalizumab (TYSABRI®); abd c.
- teriflunomide Aubagio®
- BAFIERTAM TM monomethyl fumarate
- TECFIDERA® fingolimod
- GILENYA® cladribine
- MAVENCLAD® siponimod
- DOYZENT® diroximel
- ozanimod ZEPOSIA®
- mitoxantrone NOVANTRONE®
- epilepsy / anti-seizure medications including brivaracetam (BRIVIACT®), carbamazepine (CARBATROL®), diazepam (VALIUM®), lorazepam (ATIVAN®), clonazepam (KLONOPIN®), eslicarbazepine (APTIOM®), ethosuximide (ZARONTIN®), felbamate (FELBATOL®), fenfluramine (FINTEPLA®), lacosamide (VIMPAT®),
- the disorder is chosen from multiple sclerosis, Neimanm-Pick disease, Alzheimers disease, Parkinson’s disease, amyotrophic lateral sclerosis, Lewy body dementia, frontotemporal dementia, glutamine expansion diseases such as Huntington’s disease, Kennedy’s disease, and spinocerebellar ataxia.
- the compounds, salts, tautomers, compositions, and methods disclosed herein may be useful for the treatment of neuropathy.
- the neuropathy is chosen from diabetic neuropathy and chemotherapy induced neuropathy.
- the compounds, salts, tautomers, compositions, and methods disclosed herein may be useful for the treatment of a retinal disease.
- the retinal disease is chosen from macular degeneration and retinitis.
- the compounds, salts, tautomers, compositions, and methods disclosed herein may be useful for the treatment of an injury to the CNS.
- the injury is chosen from a traumatic brain injury and stroke.
- the compounds, salts, tautomers, compositions, and methods disclosed herein may be useful for the treatment of an autoimmune disorder.
- the autoimmune disorder is chosen from ulcerative colitis, rheumatoid arthritis, psoriasis, lupus, inflammatory bowel disease.
- the compounds, salts, tautomers, compositions, and methods disclosed herein may be useful for the treatment of viral infections.
- the compounds, salts, tautomers, compositions, and methods disclosed herein may be useful for the treatment of sepsis.
- the compounds, salts, tautomers, compositions, and methods disclosed herein may be useful for the treatment of retinal degeneration.
- the compounds, salts, tautomers, compositions, and methods disclosed herein may be useful for the treatment of ischemic stroke.
- the compounds, salts, tautomers, compositions, and methods disclosed herein may be useful for the treatment of intracerebral hemorrhage.
- the compounds, salts, tautomers, compositions, and methods disclosed herein may be useful for the treatment of amyotrophic lateral sclerosis.
- the compounds, salts, tautomers, compositions, and methods disclosed herein may be useful for the treatment of an acute kidney injury.
- the compounds, salts, tautomers, compositions, and methods disclosed herein may be useful for the treatment of a myocardial reperfusion injury.
- the compounds, salts, tautomers, compositions, and methods disclosed herein may be useful for the treatment of Alzheimer’s disease.
- the compounds, salts, tautomers, compositions, and methods disclosed herein may be useful for the treatment of ulcerative colitis.
- the compounds, salts, tautomers, compositions, and methods disclosed herein may be useful for the treatment of osteoarthritis.
- the compounds, salts, tautomers, compositions, and methods disclosed herein may be useful for the treatment of myelodysplastic syndrome.
- the compounds, salts, tautomers, compositions, and methods disclosed herein may be useful for the treatment of myelodysplastic syndrome at any stage of the disease, and to retard progression of the disease, including progression to acute myeloid leukemia.
- the compounds, salts, tautomers, compositions, and methods disclosed herein may be effective to maintain the disease in complete or partial remission following treatment for such remission, for example bone marrow transplant or chemotherapy.
- the compounds, salts, tautomers, compositions, and methods disclosed herein may be useful for the treatment of one or more sub-classifications of myelodysplastic syndrome, as defined by either the FAB or WHO classifications, including refractory anemia with or without ringed sideroblasts, 5q-syndrome with or without ringed sideroblasts, refactory anemia with multilineage dysplasia with or without ringed sideroblasts, refactory anemia with excess blasts I and II, refractory anemia with excess blasts in transformation, chronic myelo-monocytic leukemia, and unclassifiable myelodysplastic syndrome.
- myelodysplastic syndrome as defined by either the FAB or WHO classifications, including refractory anemia with or without ringed sideroblasts, 5q-syndrome with or without ringed sideroblasts, refactory anemia with multilineage dysplasia with or without ringe
- the compounds, salts, tautomers, compositions, and methods disclosed herein may be useful to treat patients within one of the classifications defined by the International Prognostic Scoring System, including the low, intermediate-1, intermediate-2 and high risk classifications.
- the compounds, salts, tautomers, compositions, and methods disclosed herein may be particularly beneficial in treating patients who are within the intermediate and high risk classifications and are at increased risk of death or progression of the disease to acute myeloid leukemia.
- the compounds, salts, tautomers, compositions, and methods disclosed herein may be useful for the treatment of acute myeloid leukemia.
- the compounds, salts, tautomers, compositions, and methods disclosed herein may be useful both for the treatment of the active disease, and for maintenance of the disease in complete or partial remission following treatment for such remission, for example bone marrow transplant or chemotherapy.
- the compounds, salts, tautomers, compositions, and methods disclosed herein may be useful for the treatment of one or more sub-classifications of acute myeloid leukemia, as defined by either the FAB or WHO classifications, including minimally differentiated myeloid leukemia (MO), acute myeloid leukemia without maturation (M1), acute myeloid leukemia with maturation (M2), acute myeloid leukemia with maturation with t(8;21), acute promyelocytic leukemia (M3), hypergranular type acute myeloid leukemia, micro granular type acute myeloid leukemia.
- MO minimally differentiated myeloid leukemia
- M1 acute myeloid leukemia without maturation
- M2 acute myeloid leukemia with maturation
- M3 acute myeloid leukemia with maturation with t(8;21)
- M3 acute promyelocytic leukemia
- hypergranular type acute myeloid leukemia micro granular type acute myeloid le
- acute myelomonocytic leukemia (M4), acute myelomonocytic leukemia with increased marrow eosinophils (M4EO), acute Monocytic Leukemia (M5), acute monoblastic leukemia (M5a), acute monocytic leukemia with maturation (M5b), erythroleukemia, erythroid/myeloid leukemia (M6a), pure erythroid leukemia (M6b), acute megakaryoblastic leukemia (M7), acute megakaryoblastic leukemia associated with t(1;22), acute basophilic leukemia, acute myelofibrosis (acute myelodysplasia with myelofibrosis), acute leukemia and transient myeloproliferative disorder in Down's Syndrome, hypocellular acute myeloid leukemia, and myeloid sarcoma.
- M5a acute monoblastic leukemia with maturation
- M6a
- the compounds, salts, tautomers, compositions, and methods disclosed herein may be coadministered with another therapeutic agent.
- certain compounds salts, tautomers, and formulations disclosed herein may also be useful for veterinary treatment of companion animals, exotic animals and farm animals, including mammals, rodents, and the like. More preferred animals include horses, dogs, and cats.
- BAST bis(2-methoxyethyl)aminosulfur trifluoride
- Bu butyl
- Bu3SnH tributyltin hydride
- CD3OD deuterated methanol
- CDCl 3 deuterated chloroform
- CDI 1,1′-carbonyldiimidazole
- DAST (diethylamino)sulfur trifluoride
- dba dibenzylideneacetone
- DBU 1,8- diazabicyclo[5.4.0]undec-7-ene
- DCE 1,2-dichloroethane
- DCM dichloromethane
- DEAD diethyl azodicarboxylate
- DtBAD di-t
- Carboxaldehyde II-01 is reacted with vinyl Grignard II-02 to afford secondary alcohol II-03. Allylic rearrangement provides ketone II-04. Condensation with amide acetal II-05 provides enone II-06, which is further reacted with acetamidine to give pyrimidine II-07. Oxidation of the activated 2-methyl group gives carboxylic acid II-08, which is suitable for incorporation into Scheme I. Syntheses of certain compounds may include deprotection steps for one or more of groups R 1 , R 2 , R 3 , and R 4 , using methods known in the art. [0306] The invention is further illustrated by the following examples.
- INTERMEDIATE A-4 5-Chloro-4-(4-fluoro-3-methylphenyl)pyrimidine-2-carboxylic acid [0321] This compound was obtained using a procedure similar to that used for Intermediate A-3.
- INTERMEDIATE A-5 5-chloro-4-(2-fluorophenyl)pyrimidine-2-carboxylic acid
- 2,5-Dichloro-4-(2-fluorophenyl)pyrimidine To a solution of 2,4,5- trichloropyrimidine (3 g, 16.36 mmol, 1 eq) in THF (30 mL) and H 2 O (6 mL) were added (2- fluorophenyl) boronic acid (2.29 g, 16.36 mmol, 1 eq), Na 2 CO 3 (3.47 g, 32.71 mmol, 2 eq), PPh3 (214.50 mg, 817.78 ⁇ mol, 0.05 eq) and Pd(OAc)2 (183.60 mg, 817
- reaction mixture was filtered and concentrated under reduced pressure.
- the residue was purified by silica gel chromatography (40 g SepaFlash® Silica Flash Column, Eluent 30 ⁇ 50% EtOAC / Petroleum ether gradient @ 50 mL/min) to afford the title compound (900 mg, 3.88 mmol, 71% yield) as a red solid.
- reaction mixture was stirred and irradiated with two 34 W blue LED lamps (at approximately 7 cm away) from the light source to maintain the reaction temperature at 25 °C for 14 h.
- the mixture was diluted with water (50 mL) and extracted with EtOAc (50 mL x 2). The combined organic layers were washed with brine (50 mL x 3), dried over Na2SO4, filtered and concentrated under reduced pressure.
- the residue was purified by silica gel chromatography (40 g SepaFlash® Silica Flash Column, Eluent 10 ⁇ 25% EtOAC / Petroleum ether gradient @ 60 mL/min) to afford the title compound (390 mg, 1.20 mmol, 78% yield) as a yellow oil.
- the suspension was degassed under vacuum and purged with CO several times. After stirring under CO (15 psi) at 60 °C for 32 h, the mixture was concentrated under reduced pressure. The residue was purified by silica gel chromatography (ISCO®; 4 g SepaFlash® Silica Flash Column, Eluent 0 ⁇ 50% EtOAC / Petroleum ether gradient @ 30 mL/min) to afford the title compound (30 mg, 110.19 ⁇ mol, 54% yield) as a white solid.
- reaction mixture was filtered through CELITE®, and the filtrate was concentrated under reduced pressure to yield the title compound (90 mg, 0.369 mmol, 92 % yield) as a off-white amorphous material, which was used in the next step without further purification.
- the reaction mixture was degassed with N 2 for 10min. then (2'-amino-[1,1'-biphenyl]-2- yl)(dicyclohexyl(2',4',6'-triisopropyl-[1,1'-biphenyl]-2-yl)-l5-phosphaneyl)palladium(III) chloride (X-PhosPd G2) (7.00 mg, 8.89 ⁇ mol) was added to the mixture. The vial was sealed and the reaction mixture was heated to 140 °C in the microwave reactor for 1hr. The mixture was diluted with EtOAc, H 2 O was added, and the layers were separated.
- ADP-Glo Kinase Assay In order to measure RIPK1 activity the ADP-Glo kinase assay (Promega, Catalog #V7002) was used to measure the conversion of ATP to ADP.
- This enzymatic assay was performed in a 384-well white, Optiplate (Perkin Elmer, Catalog #6007299) with assay buffer consisting of 50mM HEPES pH 7.5 (Gibco, Catalog #15630-080), 50mM NaCl (Teknova, Catalog #S0252), 30mM MgCl 2 (Ambion, Catalog #AM9530G), 1mM DTT (Santa Cruz Biotechnology, Catalog #sc-29089), 0.05% BSA (Sigma, Catalog #A3059-50G) and 0.02% CHAPS (Sigma, Catalog #C5070-5G).
- Stock solutions of the test compounds were prepared in 100% DMSO (Sigma, Catalog #D2650) and serially diluted 1:3 using 100% DMSO.
- Compounds were additionally diluted 1:40 in assay buffer, and 2 ⁇ L / well were transferred to the assay plate.4 ⁇ L / well (final concentration of 5nM) of RIPK1 protein (SignalChem, Catalog #R07-11G-05) diluted in assay buffer and added to the assay plate followed by a 10 minute preincubation at room temperature.4 ⁇ L / well of ATP (Promega, Catalog #V7002) (final concentration of 50 ⁇ M) diluted in assay buffer were then added to the assay plate followed by a 6 hr reaction time. Final concentrations of RIPK1 and ATP refer to a 10 ⁇ L volume. Luminescence was measured using a BioTek Synergy TM NEO plate reader.
- the human monocytic cell line U937 (CRL-1593.2) may be purchased from ATCC.
- the cells are routinely maintained in RPMI-1640 Medium (Gibco, Catalog #11875- 093) supplemented with 10% heat inactivated fetal bovine serum (Gibco, Catalog #16140- 071), 100 units / mL penicillin and 100 ⁇ g / mL streptomycin (Gibco, Catalog #15140-122), in a humidified incubator (37 o C, 5% CO 2 ).
- cells are resuspended in RPMI- 1640 phenol red free Media (Gibco, Catalog # 11835-030) supplemented with 10% fetal bovine serum (Sigma, Catalog #F2442), 100units / mL penicillin and 100ug / mL streptomycin.
- Cells are stimulated with 25ng / mL human TNFalpha (Cell Sciences, Catalog #CSI15659B) and 25 ⁇ M z-VAD-FMK (R&D Systems, Catalog #FMK001) followed by seeding 5000 cells per well in a volume of 40 ⁇ L to a white, CulturPlate-384 (Perkin Elmer, Catalog #6007680).
- test compounds are prepared in 100% DMSO (Sigma, Catalog #D2650) and serially diluted 1:3 using 100% DMSO. Compounds are additionally diluted 1:40 in assay medium, and 10 ⁇ L / well was transferred to the plate. Following the compound addition, the plate is incubated at 37 o C and 5% CO 2 for 22 hr. After 22 hr, viability is assessed with the addition of 20 ⁇ L of Cell Titer-Glo 2.0 (Promega, Catalog #G9243). The tissue culture plate is shaken on an orbital shaker at 300RPM for 15 minutes at room temperature in the dark. Luminescence is measured using a PerkinElmer Envision TM plate reader.
- IC 50 values are calculated using a four-parameter logistic curve fit using Genedata Screener software. Compounds disclosed herein are expected to have activity in this assay. RIPK1 Kd determinations [0630] Compounds with lower dissociation constants bind with more affinity to the target. Compounds disclosed herein, particularly (but not exclusively) those with with lower dissociation constants, can be expected to inhibit target activity and to be useful in the treatment of RIPK1-mediated disease.
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Abstract
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MX2022010693A MX2022010693A (en) | 2020-02-28 | 2021-02-26 | Inhibitors of receptor interacting protein kinase i for the treatment of disease. |
CA3169099A CA3169099A1 (en) | 2020-02-28 | 2021-02-26 | Inhibitors of receptor interacting protein kinase i for the treatment of disease |
BR112022017099A BR112022017099A2 (en) | 2020-02-28 | 2021-02-26 | COMPOUND, PHARMACEUTICAL COMPOSITION, METHOD FOR INHIBITING RIPK1, METHOD FOR TREATMENT OF A RIPK1-MEDIATED DISEASE AND METHOD FOR TREATMENT OF CNS DAMAGE |
CN202180031531.5A CN115515940A (en) | 2020-02-28 | 2021-02-26 | Inhibitors of receptor interacting protein kinase I for the treatment of disease |
AU2021225921A AU2021225921A1 (en) | 2020-02-28 | 2021-02-26 | Inhibitors of Receptor Interacting Protein Kinase I for the treatment of disease |
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EP21760954.4A EP4110765A4 (en) | 2020-02-28 | 2021-02-26 | Inhibitors of receptor interacting protein kinase i for the treatment of disease |
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US20210154204A1 (en) * | 2019-11-26 | 2021-05-27 | Board Of Regents, The University Of Texas System | Inhibitors of receptor interacting protein kinase i for the treatment of disease |
US11718612B2 (en) | 2019-09-06 | 2023-08-08 | Board Of Regents, The University Of Texas System | Inhibitors of receptor interacting protein kinase I for the treatment of disease |
US11753381B2 (en) | 2019-09-27 | 2023-09-12 | Board Of Regents, The University Of Texas System | Inhibitors of receptor interacting protein kinase I for the treatment of disease |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20040072876A1 (en) * | 2000-12-08 | 2004-04-15 | Noritaka Kuroda | Substituted thiazole derivatives bearing 3-pyridyl groups, process for preparing the same and use thereof |
US20050032786A1 (en) * | 2001-09-03 | 2005-02-10 | Masahiro Kajino | 1, 3-benzothiazinone derivatives and use thereof |
US9029370B2 (en) * | 2011-06-10 | 2015-05-12 | Hoffmann-La Roche Inc. | Substituted benzamide derivatives |
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AU2016287581B2 (en) * | 2015-07-02 | 2019-06-06 | F. Hoffmann-La Roche Ag | Bicyclic lactams and methods of use thereof |
JP7349359B2 (en) * | 2016-10-17 | 2023-09-22 | エフ. ホフマン-ラ ロシュ アーゲー | Bicyclic pyridone lactams and methods of using them. |
MD3788044T2 (en) * | 2018-05-03 | 2023-12-31 | Rigel Pharmaceuticals Inc | RIP1 inhibitory compounds and methods for making and using the same |
CN111138448B (en) * | 2018-11-02 | 2022-08-02 | 中国科学院上海药物研究所 | Heterocyclic amides inhibiting RIP1 kinase and uses thereof |
US11718612B2 (en) * | 2019-09-06 | 2023-08-08 | Board Of Regents, The University Of Texas System | Inhibitors of receptor interacting protein kinase I for the treatment of disease |
EP4025568A1 (en) * | 2019-09-06 | 2022-07-13 | Rigel Pharmaceuticals, Inc. | Rip1 inhibitory compounds and methods for making and using the same |
AR121717A1 (en) * | 2020-04-02 | 2022-06-29 | Rigel Pharmaceuticals Inc | RIP1K INHIBITORS |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20040072876A1 (en) * | 2000-12-08 | 2004-04-15 | Noritaka Kuroda | Substituted thiazole derivatives bearing 3-pyridyl groups, process for preparing the same and use thereof |
US20050032786A1 (en) * | 2001-09-03 | 2005-02-10 | Masahiro Kajino | 1, 3-benzothiazinone derivatives and use thereof |
US9029370B2 (en) * | 2011-06-10 | 2015-05-12 | Hoffmann-La Roche Inc. | Substituted benzamide derivatives |
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---|
See also references of EP4110765A4 * |
Cited By (4)
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US11718612B2 (en) | 2019-09-06 | 2023-08-08 | Board Of Regents, The University Of Texas System | Inhibitors of receptor interacting protein kinase I for the treatment of disease |
US11753381B2 (en) | 2019-09-27 | 2023-09-12 | Board Of Regents, The University Of Texas System | Inhibitors of receptor interacting protein kinase I for the treatment of disease |
US20210154204A1 (en) * | 2019-11-26 | 2021-05-27 | Board Of Regents, The University Of Texas System | Inhibitors of receptor interacting protein kinase i for the treatment of disease |
US11690850B2 (en) * | 2019-11-26 | 2023-07-04 | Board Of Regents, The University Of Texas System | Inhibitors of receptor interacting protein kinase I for the treatment of disease |
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IL295975A (en) | 2022-10-01 |
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