Patent Grant
11535618
This disclosure relates to inhibiting Ubiquitin-Specific Protease 30 (USP30), including novel compounds and methods for inhibiting USP30. The compounds and related methods are useful in the field of medicine including the development of new therapies (e.g., for the treatment of conditions related to the therapeutic inhibition of USP30 such as Parkinson's Disease (PD)).
The ubiquitination system is a highly regulated process which affects a wide variety of cellular activities and physiological processes. Ubiquitination is a reversible process, facilitated by a group of proteins known as deubiquitinating enzymes (DUBs), which deconjugate ubiquitin (Ub) from the substrate. DUBs are encoded by approximately 100 human genes and are divided into six families, with the largest family being the ubiquitin-specific proteases (USPs) with more than 50 members.
Ubiquitination regulates mitochondrial dynamics and biogenesis, affecting the abundance and function of these organelles. Mitochondria serve many functions to maintain cell health in mammals, including generating ATP. As mitochondria age they become damaged, losing their metabolic functionality, and begin releasing pro-apoptotic proteins. Mitochondria self-regulate their quality via the mechanism of mitophagy, which is the selective removal of damaged mitochondria from the cell. Ubiquitination of mitochondrial proteins is believed to contribute to mitochondrial dynamics in mammalian cells, possibly by “flagging” those proteins for inactivation. Ubiquitin-Specific Protease 30 (USP30) is embedded in the outer membrane of mitochondria, where it participates in the maintenance of mitochondrial morphology. It is believed that over-expression of USP30 can lead to a decrease in mitophagy.
Inactivating mutations in PINK1 and Parkin can impair mitophagy and result in accumulation of damaged mitochondria and neuronal toxicity, which has been implicated in Parkinson's Disease. USP30 opposes the ligase activity of Parkin and is a negative regulator of mitophagy. USP30 inhibition is expected to promote mitophagy and restore mitochondrial health.
The disclosure provides compounds useful for inhibiting USP30, including USP30 Inhibitor Compounds as defined herein. In some embodiments, the disclosure provides a compound of formula (I):
or a pharmaceutically acceptable salt thereof, wherein
Ra, Rb, Rc, Rd, Re, Rf, Rg and Rh are defined as follows:
(i)Ra and Rb form a C1-C4 alkylene group between the atoms to which they are attached, wherein said C1-C4 alkylene group is substituted with 0-4 substituents selected from the group consisting of halogen, C1-C3 alkyl, and C1-C3 haloalkyl; and Rc, Rd, Re, Rf, Rg, and Rh are each independently hydrogen, halogen, C1-C3 alkyl, or C1-C3 haloalkyl; or
(ii) Ra and Re form a C1-C2 alkylene group between the atoms to which they are attached, wherein said C1-C2 alkylene group is substituted with 0-4 substituents selected from the group consisting of halogen, C1-C3 alkyl, and C1-C3 haloalkyl; and Rb, Rc, Rd, Rf, Rg, and Rh are each independently hydrogen, halogen, C1-C3 alkyl, or C1-C3 haloalkyl; or
(iii) Ra and Rg form a C1-C3 alkylene group between the atoms to which they are attached, wherein said C1-C3 alkylene group is substituted with 0-4 substituents selected from the group consisting of halogen, C1-C3 alkyl, and C1-C3 haloalkyl; and Rb, Rc, Rd, Re, Rf, and Rh are each independently hydrogen, halogen, C1-C3 alkyl, or C1-C3 haloalkyl; or
(iv) Rh and Rc form a C1-C4 alkylene group between the atoms to which they are attached, wherein said C1-C4 alkylene group is substituted with 0-4 substituents selected from the group consisting of halogen, C1-C3 alkyl, and C1-C3 haloalkyl; and Ra, Rd, Re, Rf, Rg, and Rh are each independently hydrogen, halogen, C1-C3 alkyl, or C1-C3 haloalkyl; or
(v) Rb and Rc form a C1-C3 alkylene group between the atoms to which they are attached, wherein said C1-C3 alkylene group is substituted with 0-4 substituents selected from the group consisting of halogen, C1-C3 alkyl, and C1-C3 haloalkyl; and Ra, Re, Rd, Rf, Rg, and Rh are each independently hydrogen, halogen, C1-C3 alkyl, or C1-C3 haloalkyl; or
(vi) Rb and Rg form a C1-C4 alkylene group between the atoms to which they are attached, wherein said C1-C4 alkylene group is substituted with 0-4 substituents selected from the group consisting of halogen, C1-C3 alkyl, and C1-C3 haloalkyl; and Ra, Re, Rd, Re, Rf, and Rh are each independently hydrogen, halogen, C1-C3 alkyl, or C1-C3 haloalkyl; or
(vii) Rc and Rd together with the atom to which they are attached, form a 3-6 membered cycloalkyl or heterocycloalkyl, wherein said 3-6 membered cycloalkyl or heterocycloalkyl is substituted with 0-4 substituents selected from the group consisting of halogen, C1-C3 alkyl, and C1-C3 haloalkyl; and Ra, Rb, Re, Rf, Rg, and Rh are each independently hydrogen, halogen, C1-C3 alkyl, or C1-C3 haloalkyl; or
(viii) Rc and Rd together form ═O; and Rd, Rb, Re, Rf, Rg, and Rh are each independently hydrogen, halogen, C1-C3 alkyl, or C1-C3 haloalkyl; or
(ix) Rc and Rc form a C1-C4 alkylene group between the atoms to which they are attached, wherein said C1-C4 alkylene group is substituted with 0-4 substituents selected from the group consisting of halogen, C1-C3 alkyl, and C1-C3 haloalkyl; and Ra, Rb, Rd, Rf, Rg, and Rh are each independently hydrogen, halogen, C1-C3 alkyl, or C1-C3 haloalkyl; or
(x) Rc and Rg form a C1-C3 alkylene group between the atoms to which they are attached, wherein said C1-C3 alkylene group is substituted with 0-4 substituents selected from the group consisting of halogen, C1-C3 alkyl, and C1-C3 haloalkyl, and Ra, Rb, Rd, Re, Rf, and Rh are each independently hydrogen, halogen, C1-C3 alkyl, or C1-C3 haloalkyl; or
(xi) Re and Rf together with the atom to which they are attached, form a 3-6 membered cycloalkyl or heterocycloalkyl, wherein said 3-6 membered cycloalkyl or heterocycloalkyl is substituted with 0-4 substituents selected from the group consisting of halogen, C1-C3 alkyl, and C1-C3 haloalkyl; and Ra, Rb, Rc, Rd, Rg, and Rh are each independently hydrogen, halogen, C1-C3 alkyl, or C1-C3 haloalkyl; or
(xii) Rc and Rf together form ═O; and Ra, Rb, Rc, Rd, Rg, and Rh are each independently hydrogen, halogen, C1-C3 alkyl, or C1-C3 haloalkyl; or
(xiii) Re and Rg form a C1-C3 alkylene group between the atoms to which they are attached, wherein said C1-C3 alkylene group is substituted with 0-4 substituents selected from the group consisting of halogen, C1-C3 alkyl, and C1-C3 haloalkyl; and Ra, Rb, Rc, Rd, Rf, and Rh are each independently hydrogen, halogen, C1-C3 alkyl, or C1-C3 haloalkyl; or
(xiv) Rg and Rh together with the atom to which they are attached, form a 3-6 membered cycloalkyl or heterocycloalkyl, wherein said 3-6 membered cycloalkyl or heterocycloalkyl is substituted with 0-4 substituents selected from the group consisting of halogen, C1-C3 alkyl, and C1-C3 haloalkyl; and Ra, Rb, Rc, Rd, Re, and Rf are each independently hydrogen, halogen, C1-C3 alkyl, or C1-C3 haloalkyl; or
(xv) Rg and Rh together form ═O; and Ra, Rb, Rc, Rd, Re, and Rf are each independently hydrogen, halogen, C1-C3 alkyl, or C1-C3 haloalkyl; and
Ar1 is phenylene or 5-6 membered heteroarylene, wherein said phenylene or heteroarylene is substituted with m 10 groups; and
Ar2 is phenylene or 5-10 membered heteroarylene, wherein said phenylene or heteroarylene is substituted with n R2 groups;
L is —O—, —S—, —NR3—, —C(R4)2—, —S(O)2—, or —S(O)—;
M is C1-C6 alkyl, C1-C6 haloalkyl, 3-6 membered cycloalkyl, phenyl, or 5-6 membered heteroaryl, wherein said cycloalkyl, phenyl, or heteroaryl is substituted with p R5 groups;
each occurrence of R1, R2, and R5 is independently halo, cyano, NO2, oxo, hydroxyl, —R6, —OR6, C1-C6 alkyl, C1-C6 haloalkyl, C1-C6 hydroxyalkyl, —C1-C6 alkylene-R6, C1-C6 alkoxy, C1-C6 haloalkoxy, —C0-C3 alkylene-NR6R7, —C0-C3 alkylene-NR7R8, —C0-C3 alkylene-C(O)NR6R7, —C0-C3 alkylene-C(O)NR7W, —C0-C3 alkylene-NR7C(O)R6, —C0-C3 alkylene-NR7C(O)W, —C0-C3 alkylene-NR7S(O)2R6, —C0-C3 alkylene-C(O)R6, —C0-C3 alkylene-C(O)R7, —C0-C3 alkylene-SR6, —C0-C3 alkylene-S(O)R6, —C0-C3 alkylene-S(O)2R6, —C0-C3 alkylene-S(O)2R7, —C0-C3 alkylene-S(O)2NR6R7, —C0-C3 alkylene-S(O)2NR7R8, —C0-C3 alkylene-NR7C(O)NR8R9, —C0-C3 alkylene- NR7S(O)2NR8R9, —C0-C3 alkylene-C(O)OR7, —C0-C3 alkylene-C(O)OR6, —C0-C3 alkylene-OC(O)R7, —C0-C3 alkylene-OC(O)R6, —C0-C3 alkylene-NR7C(O)OR8, or —C0-C3 alkylene-NR7S(O)2R8;
R3 is H, C1-C6 alkyl, or C1-C6 haloalkyl;
each R4 is independently H, C1-C6 alkyl, or C1-C6 haloalkyl, or two R4 groups together with the carbon atom to which they are attached form a 3-6 membered cycloalkyl or heterocycloalkyl;
each R6 is independently 5-10 membered heteroaryl, 4-10 membered heterocycloalkyl, 6-10 membered aryl, or 3-8 membered cycloalkyl, wherein said heteroaryl, heterocycloalkyl, aryl, or cycloalkyl is optionally substituted with 1-5 substituents independently selected from the group consisting of halo, oxo, C1-C6 alkyl, C1-C6 haloalkyl, C1-C6 hydroxyalkyl, C1-C6 alkoxy, C1-C6 haloalkoxy, C2-C6 alkenyl, C2-C6 alkynyl, 5-10 membered heteroaryl, 4-10 membered heterocycloalkyl, 6-10 membered aryl, 3-8 membered cycloalkyl, —NR10C(O)NR11R12, —NR10R11, —C(O)R10, —NR10C(O)R11, —NR10C(O)OR11, —S(O)2R10, —C(O)NR10R11, —C(O)OR10, —S(O)2NR10R11, —NR10S(O)2R11, —OR10, —OC(O)R10, —OS(O)2R10, —OC(O)NR10R11, —OC(O)OR10, —OS(O)2NR10R11, —C(O)NR10C(O)NR11R12, —C(O)C(O)R10, —C(O)NR10C(O)R11, —C(O)NR10C(O)OR11, —C(O)S(O)2R10, —C(O)C(O)NR10R11, —C(O)C(O)OR10, —C(O)S(O)2NR10R11, —C(O)NR10S(O)2R11, —C1-C6 alkylene-R10, —C1-C6 alkylene-NR10C(O)NR11R12, —C1-C6 alkylene- NR10NR11, —C1-C6 alkylene-C(O)R10, —C1-C6 alkylene-NR10C(O)R11, —C1-C6 alkylene-NR10C(O)OR11, —C1-C6 alkylene-S(O)2R10, —C1-C6 alkylene-C(O)NR10R11, —C1-C6 alkylene-C(O)OR10, —C1-C6 alkylene-S(O)2NR10R11, —C1-C6 alkylene-NR10S(O)2R11, —C1-C6 alkenylene-R10, —C1-C6 alkenylene-NR10C(O)NR11102, —C1-C6 alkenylene-NR10R11, —C1-C6 alkenylene-C(O)R10, —C1-C6 alkenylene-NR10C(O)R11, —C1-C6 alkenylene-NR10C(O)OR11, —C1-C6 alkenylene-S(O)2R10, —C1-C6 alkenylene-C(O)NR10R11, —C1-C6 alkenylene-C(O)OR10, —C1-C6 alkenylene-S(O)2NR10R11, and —C1-C6 alkenylene-NR10S(O)2R11;
each R7, R8, and R9 is independently hydrogen or C1-C6 alkyl;
each R10, R11, and R12 is independently hydrogen, C1-C6 alkyl, 5-10 membered heteroaryl, 4-10 membered heterocycloalkyl, 6-10 membered aryl, or 3-8 membered cycloalkyl;
m is 0-4;
n is 0-4; and
p is 0-4.
In some embodiments, the disclosure provides a compound of formula (I-C):
or a pharmaceutically acceptable salt thereof, wherein R2, R5, n, Ra, Rb, Rc, Rd, Re, Rf, Rg, and Rh are all as defined for formula (I) above and described in classes and subclasses herein for formula (I), both singly and in combination.
In some embodiments, a USP30 Inhibitor Compound is a compound selected from the group consisting of:
wherein R2, R5, n, and p are as defined with respect to formula (I) herein, or a pharmaceutically acceptable salt thereof, having an IC50 value of about ≤1 μM (and preferably ≤0.5 μM or ≤0.1 04) and >0.001 μM as measured in a Ubiquitin-Rhodamine 110 Assay as described in Example 1. In some embodiments, compounds of formula (I-C) are provided where R2 and R5 are both hydrogen.
In some embodiments, a USP30 Inhibitor Compound is a compound of the chemical formula:
wherein R2, R5, n, and p are as defined with respect to formula (I) herein, or a pharmaceutically acceptable salt thereof, having an IC50 value of about ≤1 μM (and preferably ≤0.5 μM or ≤0.1 μM) and >0.001 μM as measured in a Ubiquitin-Rhodamine 110 Assay as described in Example 1.
In some embodiments, a compound is any compound selected from the compounds listed in Table 1 herein.
The present disclosure relates to compounds of formula (I), as defined herein, pharmaceutically acceptable salts thereof, pharmaceutical compositions comprising same, and medical uses involving same. In some embodiments, the compounds of formula (I) are USP30 Inhibitor Compounds. In other embodiments, the compounds of formula (I) are useful, for example, as analytical tools and/or control compounds in biological assays (e.g., compounds of any of the following aspects and embodiments that are not USP30 Inhibitor Compounds).
USP30 Inhibitor Compounds are useful in the development of new therapies for Parkinson's disease (PD), and in methods of treating diseases or conditions by inhibiting USP30 (such as PD). Parkin (E3 ubiquitin ligase) and PINK1 (kinase) are key regulators of mitophagy. In healthy mitochondria, PINK1 localization to the mitochondrial outer membrane (MOM) and exposure to the cytosol is limited by rapid import to the mitochondrial inner membrane (MIM). Once localized to the MIM, PINK1 is processed by several proteases, such as presenilin associated rhomboid-like protease (PARL), to yield a truncated version of PINK1 which is subsequently degraded by the proteasome (Meissner et al., Autophagy. 2015, 11(9), 1484-1498). Upon mitochondrial depolarization or dysfunction, PINK1 accumulates in the MOM, recruiting and activating Parkin via PINK1-dependent phosphorylation of both ubiquitin and Parkin. Consequently, activated Parkin ubiquitinates MOM proteins like TOMM20 to trigger mitophagy (Pickrell et al., Neuron. 2015, 85(2), 257-273). USP30 is embedded in the MOM with its catalytic DUB domain oriented towards the cytosol and has been shown to antagonize Parkin-mediated ubiquitination of common substrates, consequently opposing Parkin-mediated mitophagy. Genetic silencing of USP30 results in increased ubiquitination of several Parkin substrates followed by increased mitophagy. In model organisms, USP30 depletion is able to rescue mitophagy defects caused by pathogenic Parkin mutations, as well as restore mitochondria morphology and function, and dopamine levels. (Nakamura, et al., Mol Biol Cell. 2008, 19(5), 1903-1911; Bingol, et al., Nature 2014, 510(7505):370-5). Therefore, inhibition of USP30 with a compound disclosed herein could present a novel treatment paradigm for PD by promoting mitochondrial turnover.
Definitions
As used herein, the term “alkyl” means a substituted or unsubstituted hydrocarbon chain that is completely saturated, including straight-chain alkyl groups and branched-chain alkyl groups, and that has a single point of attachment to the rest of the molecule. In some embodiments, a straight chain or branched chain alkyl has about 1-20 carbon atoms in its backbone (e.g., C1-C20 for straight chain, C2-C20 for branched chain), and alternatively, about 1-10. In some embodiments, an alkyl has about 1-8 carbon atoms. In some embodiments, an alkyl has about 1-6 carbon atoms. In some embodiments, an alkyl has about 1-5 carbon atoms. In some embodiments, an alkyl has about 1-4 carbon atoms. In some embodiments, an alkyl has about 1-3 carbon atoms. In some embodiments, an alkyl has about 1-2 carbon atoms.
As used herein, the term “alkylene” refers to a bivalent alkyl group. Exemplary alkylenes include —CH2—, —CH2CH2—, —CH(CH3)—, —CH2CH(CH3)—, —CH(CH3)CH3)—, etc. In some embodiments, an “alkylene chain” is a polymethylene group, i.e., —(CH2)n—, wherein n is a positive integer, preferably from 1 to 6, from 1 to 4, from 1 to 3, from 1 to 2, or from 2 to 3. A substituted alkylene chain is a polymethylene group in which one or more methylene hydrogen atoms are replaced with a substituent.
As used herein, the term “alkenyl” refers to an alkyl group, as defined herein, having one or more double bonds.
As used herein, the term “alkenylene” refers to a bivalent alkenyl group. A substituted alkenylene chain is a polymethylene group containing at least one double bond in which one or more hydrogen atoms are replaced with a substituent.
As used herein, the term “alkynyl” refers to an alkyl group, as defined herein, having one or more triple bonds.
The term “aryl” refers to ring systems having a total of five to fourteen ring members, wherein at least one ring in the system is aromatic and wherein each ring in the system contains 3 to 7 ring members. The term “aryl” may be used interchangeably with the term “aryl ring.” In certain embodiments of the present disclosure, “aryl” refers to an aromatic ring system and exemplary groups include phenyl, biphenyl, naphthyl, anthracyl and the like, which may bear one or more substituents. Also included within the scope of the term “aryl,” as it is used herein, is a group in which an aromatic ring is fused to one or more non-aromatic rings, such as indanyl, phthalimidyl, naphthimidyl, phenanthridinyl, or tetrahydronaphthyl, and the like.
The term “arylene” refers to a bivalent aryl group (e.g., phenylene).
As used herein, the term “cycloalkyl” refers to a cyclic alkyl group (e.g., a monocyclic alkyl group or a bicyclic alkyl group). In some embodiments, “cycloalkyl” refers to a monocyclic C3-C8 cycloalkyl group. In some embodiments, “cycloalkyl” refers to a monocyclic C3-C6 cycloalkyl group.
The terms “halogen” or “halo” mean F, Cl, Br, or I.
The term “heteroaryl” refer to groups having 5 to 10 ring atoms, preferably 5, 6, or 9 ring atoms; having 6, 10, or 14 π electrons shared in a cyclic array; and having, in addition to carbon atoms, from one to five heteroatoms wherein the term “heteroatom” refers to nitrogen, oxygen, or sulfur, and includes any oxidized form of nitrogen or sulfur, and any quaternized form of a basic nitrogen. Exemplary heteroaryl groups include thienyl, furanyl, pyrrolyl, imidazolyl, pyrazolyl, triazolyl, tetrazolyl, oxazolyl, isoxazolyl, oxadiazolyl, thiazolyl, isothiazolyl, thiadiazolyl, pyridyl, pyridazinyl, pyrimidinyl, pyrazinyl, indolizinyl, purinyl, naphthyridinyl, and pteridinyl. The term “heteroaryl”, as used herein, also includes groups in which a heteroaromatic ring is fused to one or more aryl, cycloaliphatic, or heterocyclyl rings, where the radical or point of attachment is on the heteroaromatic ring. Examplary groups include indolyl, isoindolyl, benzothienyl, benzofuranyl, dibenzofuranyl, indazolyl, benzimidazolyl, benzthiazolyl, quinolyl, isoquinolyl, cinnolinyl, phthalazinyl, quinazolinyl, quinoxalinyl, 4H-quinolizinyl, carbazolyl, acridinyl, phenazinyl, phenothiazinyl, phenoxazinyl, tetrahydroquinolinyl, tetrahydroisoquinolinyl, and pyrido[2,3-b]-1,4-oxazin-3(4H)-one. A heteroaryl group may be mono- or bicyclic. The term “heteroaryl” may be used interchangeably with the terms “heteroaryl ring,” “heteroaryl group,” or “heteroaromatic,” any of which terms include rings that are optionally substituted.
The term “heteroarylene” refers to a bivalent heteroaryl group.
As used herein, the term “heterocycloalkyl” refers to a stable 3- to 7-membered monocyclic or 7- to 10-membered bicyclic cyclic moiety that is saturated and having, in addition to carbon atoms, one or more, preferably one to four, heteroatoms independently selected from nitrogen, oxygen, and sulfur, including any oxidized form of nitrogen or sulfur, and any quaternized form of a basic nitrogen. As an example, in a saturated ring having 1-3 heteroatoms selected from oxygen, sulfur or nitrogen, the nitrogen may be N (as in 3,4-dihydro-2H-pyrrolyl), NH (as in pyrrolidinyl), or +NR (as in N-substituted pyrrolidinyl). A heterocycloalkyl ring can be attached to its pendant group at any heteroatom or carbon atom that results in a stable structure and any of the ring atoms can be optionally substituted. Examples of such heterocycloalkyl radicals include tetrahydrofuranyl, tetrahydrothiophenyl pyrrolidinyl, piperidinyl, pyrrolinyl, tetrahydroquinolinyl, tetrahydroisoquinolinyl, decahydroquinolinyl, oxazolidinyl, piperazinyl, dioxanyl, dioxolanyl, diazepinyl, oxazepinyl, thiazepinyl, morpholinyl, and quinuclidinyl. The term “heterocycloalkyl” also includes groups in which a heterocycloalkyl ring is fused to one or more aryl, heteroaryl, or cycloaliphatic rings, such as indolinyl, 3H-indolyl, chromanyl, phenanthridinyl, or tetrahydroquinolinyl, where the radical or point of attachment is on the heterocycloalkyl ring.
As used herein, a “USP30 Inhibitor Compound” refers to a compound having an IC50 of about 1 micromolar or less (i.e., an IC50 value of ≤1 μM and >0.001 μM) in the Ubiquitin-Rhodamine 110 Assay for USP30 as described in Example 1 herein. For example, a USP30 Inhibitor can be a compound of formula (I) having an IC50 value of ≤0.5 μM and >0.001 μM when tested in the Biochemical Assay of Example 1. In some embodiments, a USP30 Inhibitor is a compound of formula (I) having an IC50 value of ≤0.1 μM and >0.001 μM when tested in the Biochemical Assay of Example 1.
As used herein, the term “pharmaceutically acceptable salt” refers to salts of such compounds that are appropriate for use in pharmaceutical contexts, i.e., salts which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of humans and lower animals without undue toxicity, irritation, allergic response and the like, and are commensurate with a reasonable benefit/risk ratio. Pharmaceutically acceptable salts are well known in the art. For example, S. M. Berge, et al. describes pharmaceutically acceptable salts in detail in J. Pharmaceutical Sciences, 66: 1-19 (1977).
Unless otherwise stated, all chemical structures and chemical names depicted herein without stereochemical descriptors shall be understood to include all stereoisomeric (e.g., enantiomeric or diastereomeric) forms of the compound depicted by the structure or name, as well as all geometric and conformational isomeric forms of the compound; for example, the R and S configurations for each stereocenter. Unless otherwise stated, such structures and names shall be understood to include a stereochemically pure form of the compound and any mixture of enantiomers, diastereomers, or geometric (or conformational) isomers. Unless otherwise stated, all tautomeric forms of the compounds of the disclosure are within the scope of the disclosure.
Unless otherwise stated, all chemical structures and chemical names depicted herein with stereochemical descriptors (i.e., hash and wedge bonds in the chemical structures; (R)- and (S)-designators in the chemical names) shall be understood to refer to a compound having the relative stereochemistry (but not necessarily the absolute stereochemistry) indicated by the stereochemical descriptors. Unless otherwise stated, such structures and names shall be understood to include an enantiomerically pure form of the compound having the relative stereochemistry indicated by the stereochemical descriptors or any mixture of enantiomers. In some embodiments, the enantiomers are present in a racemic mixture. In other embodiments, the enantiomer having the absolute stereochemistry suggested by the stereochemical descriptors is present in substantially enantiomerically pure form. In other embodiments, the enantiomer having the absolute stereochemistry opposite to that suggested by the stereochemical descriptors is present in substantially enantiomerically pure form.
Unless otherwise stated, all chemical structures and chemical names depicted herein with stereochemical descriptors (i.e., hash and wedge bonds in the chemical structures; (R)- and (S)-designators in the chemical names) and an “absolute” descriptor (“abs”) shall be understood to refer to a compound having the absolute stereochemistry indicated by the stereochemical descriptors. Unless otherwise stated, such structures and names shall be understood to include the compound in enantiomerically pure form or in a mixture with its enantiomer. In some embodiments, the enantiomers are present in a racemic mixture. In other embodiments, the enantiomer having the absolute stereochemistry indicated by the stereochemical descriptors is present in substantially enantiomerically pure form.
Unless otherwise stated, structures depicted herein are also meant to include compounds that differ only in the presence of one or more isotopically enriched atoms. For example, compounds having the present structures including the replacement of hydrogen by deuterium or tritium, or the replacement of a carbon by a 13C- or 14C-enriched carbon are within the scope of this disclosure.
It will be appreciated that throughout the present disclosure, unless otherwise indicated, reference to a compound of formula (I) is intended to also include formulas I-1, I-2, I-3, I-4, I-A, I-A-1, I-A-2, I-A-3, I-A-4, I-B, I-B-1, I-B-2, I-B-3, I-B-4, I-C, I-C-1, I-C-2, I-C-3, I-C-4, I-C-a, I-C-b, I-C-c, I-C-d, I-C-e, I-C-f, I-D, I-E, I-E-1, I-E-2, I-E-3, I-E-4, I-F-1, I-F-2, I-G-1, I-G-2, I-H-1, I-H-2, I-J-1, I-J-2, I-K-1, I-K-2, I-L-1, I-L-2, I-M, I-M-1, I-M-2, I-M-3, and I-M-4, and compound species of such formulas disclosed herein.
Compounds of the Disclosure
In one aspect, the disclosure relates to a compound of formula (I):
or a pharmaceutically acceptable salt thereof, wherein Ar1, Ar2, M, L, Ra, Rb, Rc, Rd, Re, Rf, Rg, and Rh are all as defined for formula (I) above.
In some embodiments, the present disclosure provides compounds, or pharmaceutically acceptable salts thereof, of formula (I-1):
wherein Ar1, Ar2, M, L, Ra, Rd, Re, Rf, Rg, and Rh are all as defined for formula (I) above and described in classes and subclasses herein for formula (I), both singly and in combination, and
In some embodiments, the present disclosure provides compounds, or pharmaceutically acceptable salts thereof, of formula (I-2):
wherein Ar1, Ar2, M, L, Ra, Rd, Re, Rf, Rg, and Rh are all as defined for formula (I) above and described in classes and subclasses herein for formula (I), both singly and in combination, and
In some embodiments, the present disclosure provides compounds, or pharmaceutically acceptable salts thereof, of formula (I-3)
wherein Ar1, Ar2, M, L, Ra, Rd, Re, Rf, Rg, and Rh are all as defined for formula (I) above and described in classes and subclasses herein for formula (I), both singly and in combination, and
In some embodiments, the present disclosure provides compounds, or pharmaceutically acceptable salts thereof, of formula (I-4)
wherein Ar1, Ar2, M, L, Ra, Rb, Rd, Rf, Rg and Rh are all as defined for formula (I) above and described in classes and subclasses herein for formula (I), both singly and in combination, and
In another aspect, the disclosure relates to a compound of formula (I-A):
or a pharmaceutically acceptable salt thereof, wherein:
X1 is C or N;
X2 is CH, CR1, O, S, N, NH, or NR1, as valency permits;
X3 is CH, CR1, O, S, N, NH, or NR1, as valency permits;
X4 is C or N;
X5 is a bond, CH, CR1, O, S, N, NH, or NR1, as valency permits;
X6 is CH, CR1, O, S, N, NH, or NR1, as valency permits;
Y1 is C or N;
Y2 is C or N;
Y3 is CH, CR2, O, S, N, NH, or NR2, as valency permits;
Y4 is a bond, CH, CR2, O, S, N, NH, or NR2, as valency permits;
Y5 is CH, CR2, O, S, N, NH, or NR2, as valency permits;
Y6 is CH, CR2, O, S, N, NH, or NR2, as valency permits,
provided that the ring comprising X1, X2, X3, X4, X5, and X6 is aromatic, and
that the ring comprising Y1, Y2, Y3, Y4, Y5 and Y6 is aromatic;
In some embodiments, the present disclosure provides compounds, or pharmaceutically acceptable salts thereof, of formula (I-A-1):
wherein M, L, X1, X2, X3, X4, X5, X6, Y1, Y2, Y3, Y4, Y5, Ra, Rd, Re, Rf, Rg, and Rh are all as defined for formula (I-A) above and described in classes and subclasses herein for formula (I-A), both singly and in combination, and
In some embodiments, the present disclosure provides compounds, or pharmaceutically acceptable salts thereof, of formula (I-A-2):
wherein M, L, X1, X2, X3, X4, X5, X6, Y1, Y2, Y3, Y4, Y5, Y6, Ra, Rd, Re, Rf, Rg and Rh are all as defined for formula (I-A) above and described in classes and subclasses herein for formula
(I-A), both singly and in combination, and
In some embodiments, the present disclosure provides compounds, or pharmaceutically acceptable salts thereof, of formula (I-A-3):
wherein M, L, X1, X2, X3, X4, X5, X6, Y1, Y2, Y3, Y4, Y5, Y6, Ra, Rd, Re, Rf, Rg, and Rh are all as defined for formula (I-A) above and described in classes and subclasses herein for formula
(I-A), both singly and in combination, and
In some embodiments, the present disclosure provides compounds, or pharmaceutically acceptable salts thereof, of formula (I-A-4):
wherein M, L, X1, X2, X3, X4, X5, X6, Y1, Y2, Y4, Y6, Ra, Rb, Rd, Rf, Rg and Rh are all as defined for formula (I-A) above and described in classes and subclasses herein for formula
(I-A), both singly and in combination, and
In another aspect, the disclosure relates to a compound of formula (I-B):
or a pharmaceutically acceptable salt thereof, wherein:
Y3 is CH, CR2, or N;
Y4 is CH, CR2, or N;
Y5 is CH, CR2, or N;
Y6 is CH, CR2, or N; and
In some embodiments, the present disclosure provides compounds, or pharmaceutically acceptable salts thereof, of formula (I-B-1):
wherein M, L, X1, X2, X3, X4, X6, Y3, Y4, Y5, Y6, Ra, Rd, Re, Rf, Rg, and Rh are all as defined for formula (I-B) above and described in classes and subclasses herein for formula (I-B), both singly and in combination, and
In some embodiments, the present disclosure provides compounds, or pharmaceutically acceptable salts thereof, of formula (I-B-2):
wherein M, L, X1, X2, X3, X4, X6, Y3, Y4, Y5, Y6, Ra, Rd, Re, Rf, Rg, and Rh are all as defined for formula (I-B) above and described in classes and subclasses herein for formula (I-B), both singly and in combination, and
In some embodiments, the present disclosure provides compounds, or pharmaceutically acceptable salts thereof, of formula (I-B-3):
wherein M, L, X1, X2, X3, X4, X6, Y3, Y4, Y5, Y6, Ra, Rd, Re, Rf, Rg, and Rh are all as defined for formula (I-B) above and described in classes and subclasses herein for formula (I-B), both singly and in combination, and
In some embodiments, the present disclosure provides compounds, or pharmaceutically acceptable salts thereof, of formula (I-B-4):
wherein M, L, X1, X2, X3, X4, X6, Y3, Y4, Y5, Y6, Ra, Rd, Re, Rf, Rg, and Rh are all as defined for formula (I-B) above and described in classes and subclasses herein for formula (I-B), both singly and in combination, and
In another aspect, the disclosure relates to a compound of formula (I-C):
or a pharmaceutically acceptable salt thereof, wherein R2, R5, n, p, Ra, Rb, Rc, Rd, Re, Rf, Rg and Rh are all as defined for formula (I) above and described in classes and subclasses herein for formula (I), both singly and in combination.
In some embodiments, the present disclosure provides compounds, or pharmaceutically acceptable salts thereof, of formula (I-C-1):
wherein R2, R5, n, p, Ra, Rd, Re, Rf, Rg, and Rh are all as defined for formula (I-C) above and described in classes and subclasses herein for formula (I-C), both singly and in combination, and
In some embodiments, the present disclosure provides compounds, or pharmaceutically acceptable salts thereof, of formula (I-C-2):
wherein R2, R5, n, p, Ra, Rd, Re, Rf, Rg, and Rh are all as defined for formula (I-C) above and described in classes and subclasses herein for formula (I-C), both singly and in combination, and
In some embodiments, the present disclosure provides compounds, or pharmaceutically acceptable salts thereof, of formula (I-C-3):
wherein R2, R5, n, p, Ra, Rd, Re, Rf, Rg, and Rh are all as defined for formula (I-C) above and described in classes and subclasses herein for formula (I-C), both singly and in combination, and
In some embodiments, the present disclosure provides compounds, or pharmaceutically acceptable salts thereof, of formula (I-C-4):
wherein R2, R5, n, p, Ra, Rb, Rd, Rf, Rg, and Rh are all as defined for formula (I-C) above and described in classes and subclasses herein for formula (I-C), both singly and in combination, and
In some embodiments, the disclosure relates to a compound of formula (I-C), or a pharmaceutically acceptable salt thereof, wherein the compound is of formula (I-C-a):
wherein R2, R5, n, and p are all as defined for formula (I-C) above and described in classes and subclasses herein for formula (I-C), both singly and in combination.
In some embodiments, the disclosure relates to a compound of formula (I-C), or a pharmaceutically acceptable salt thereof, wherein the compound is of formula (I-C-b):
wherein R2, R5, n, and p are all as defined for formula (I-C) above and described in classes and subclasses herein for formula (I-C), both singly and in combination.
In some embodiments, the disclosure relates to a compound of formula (I-C), or a pharmaceutically acceptable salt thereof, wherein the compound is of formula (I-C-c):
wherein R2, R5, n, and p are all as defined for formula (I-C) above and described in classes and subclasses herein for formula (I-C), both singly and in combination.
In some embodiments, the disclosure relates to a compound of formula (I-C), or a pharmaceutically acceptable salt thereof, wherein the compound is of formula (I-C-d):
wherein R2, R5, n, and p are all as defined for formula (I-C) above and described in classes and subclasses herein for formula (I-C), both singly and in combination.
In some embodiments, the disclosure relates to a compound of formula (I-C), or a pharmaceutically acceptable salt thereof, wherein the compound is of formula (I-C-e):
wherein R2, R5, n, and p are all as defined for formula (I-C) above and described in classes and subclasses herein for formula (I-C), both singly and in combination.
In some embodiments, the disclosure relates to a compound of formula (I-C), or a pharmaceutically acceptable salt thereof, wherein the compound is of formula (I-C-f):
wherein R2, R5, n, and p are all as defined for formula (I-C) above and described in classes and subclasses herein for formula (I-C), both singly and in combination.
In another aspect, the disclosure relates to a compound of formula (I-D):
or a pharmaceutically acceptable salt thereof, wherein Ra, Rb, Rc, Rd, Re, Rf, Rg and Rh are all as defined for formula (I) above and described in classes and subclasses herein for formula (I), both singly and in combination.
In another aspect, the disclosure relates to a compound of formula (I-E):
or a pharmaceutically acceptable salt thereof, wherein Ra, Rb, Rc, Rd, Re, Rf and Rg are all as defined for formula (I) above and described in classes and subclasses herein for formula (I), both singly and in combination. In some embodiments, the present disclosure provides compounds, or pharmaceutically acceptable salts thereof, of formula (I-E-1):
In some embodiments, the compound of formula (I-E-1) has the absolute stereochemistry of the first eluting isomer when a racemic mixture of the compound of formula (I-E-1) is separated by the procedure described in Example 3, Step 6. In some embodiments, the compound of formula (I-E-1) has the absolute stereochemistry of the second eluting isomer when a racemic mixture of the compound of formula (I-E-1) is separated by the procedure described in Example 3, Step 6.
In some embodiments, the compound of formula (I-E-1) is:
In some embodiments, the compound of formula (I-E-1) is:
In some embodiments, the present disclosure provides compounds, or pharmaceutically acceptable salts thereof, of formula (I-E-2):
In some embodiments, the compound of formula (I-E-2) has the absolute stereochemistry of the first eluting isomer when a racemic mixture of the compound of formula (I-E-2) is separated by the procedure described in Example 4, Step 6. In some embodiments, the compound of formula (I-E-2) has the absolute stereochemistry of the second eluting isomer when a racemic mixture of the compound of formula (I-E-2) is separated by the procedure described in Example 4, Step 6.
In some embodiments, the compound of formula (I-E-2) is:
In some embodiments, the compound of formula (I-E-2) is:
In some embodiments, the present disclosure provides compounds, or pharmaceutically acceptable salts thereof, of formula (I-E-3):
In some embodiments, the compound of formula (I-E-3) has the absolute stereochemistry of the first eluting isomer when a racemic mixture of the compound of formula (I-E-3) is separated by the procedure described in Example 2, Step 7. In some embodiments, the compound of formula (I-E-3) has the absolute stereochemistry of the second eluting isomer when a racemic mixture of the compound of formula (I-E-3) is separated by the procedure described in Example 2, Step 7.
In some embodiments, the compound of formula (I-E-3) is:
In some embodiments, the compound of formula (I-E-3) is:
In some embodiments, the present disclosure provides compounds, or pharmaceutically acceptable salts thereof, of formula (I-E-4):
In some embodiments, the compound of formula (I-E-4) has the absolute stereochemistry of the first eluting isomer when a racemic mixture of the compound of formula (I-E-4) is separated by the procedure described in Example 2, Step 7. In some embodiments, the compound of formula (I-E-4) has the absolute stereochemistry of the second eluting isomer when a racemic mixture of the compound of formula (I-E-4) is separated by the procedure described in Example 2, Step 7.
In some embodiments, the compound of formula (I-E-4) is:
In some embodiments, the compound of formula (I-E-4) is:
In another aspect, the disclosure relates to a compound of formula (I-F-1) or (I-F-2):
or a pharmaceutically acceptable salt thereof, wherein X1, X2, X3, X4, X5, X6, Y1, Y2, Y3, Y4, Y5, Y6, L, and M are all as defined for formula (I-A) above and described in classes and subclasses herein for formula (I-A), both singly and in combination.
In some embodiments, the compounds of formula (I-F-1) and (I-F-2) are present in a racemic mixture. In other embodiments, the compound of formula (I-F-1) or (I-F-2) is present in substantially enantiomerically pure form. The compounds of formula (I-F-1) and (I-F-2) can be separated from one another by chiral HPLC, such as by the procedure described in Example 2, Step 7 or Example 3, Step 6.
In another aspect, the disclosure relates to a compound of formula (I-G-1) or (I-G-2):
or a pharmaceutically acceptable salt thereof, wherein X1, X2, X3, X4, X5, X6, Y1, Y2, Y3, Y4, Y5, Y6, L, and M are all as defined for formula (I-A) above and described in classes and subclasses herein for formula (I-A), both singly and in combination.
In some embodiments, the compounds of formula (I-G-1) and (I-G-2) are present in a racemic mixture. In other embodiments, the compound of formula (I-G-1) or (I-G-2) is present in substantially enantiomerically pure form. The compounds of formula (I-G-1) and (I-G-2) can be separated from one another by chiral HPLC, such as by the procedure described in Example 2, Step 7, or Example 4, Step 6.
In another aspect, the disclosure relates to a compound of formula (I-H-1) or (I-H-2):
or a pharmaceutically acceptable salt thereof, wherein X1, X2, X3, X4, X5, X6, Y1, Y2, Y3, Y4, Y5, Y6, L, and M are all as defined for formula (I-A) above and described in classes and subclasses herein for formula (I-A), both singly and in combination.
In some embodiments, the compounds of formula (I-H-1) and (I-H-2) are present in a racemic mixture. In other embodiments, the compound of formula (I-H-1) or (I-H-2) is present in substantially enantiomerically pure form. The compounds of formula (I-H-1) and (I-H-2) can be separated from one another by chiral HPLC, such as by the procedure described in Example 2, Step 7.
In another aspect, the disclosure relates to a compound of formula (I-J-1) or (I-J-2):
or a pharmaceutically acceptable salt thereof, wherein X1, X2, X3, X4, X5, X6, Y1, Y2, Y4, Y5, Y6, L, and M are all as defined for formula (I-A) above and described in classes and subclasses herein for formula (I-A), both singly and in combination.
In some embodiments, the compounds of formula (I-J-1) and (I-J-2) are present in a racemic mixture. In other embodiments, the compound of formula (I-J-1) or (I-J-2) is present in substantially enantiomerically pure form. The compounds of formula (I-J-1) and (I-J-2) can be separated from one another by chiral HPLC, such as by the procedure described in Example 2, Step 7.
In some embodiments, the present disclosure provides compounds, or pharmaceutically acceptable salts thereof, of formula (I-K-1) or (I-K-2):
wherein M, L, X1, X2, X3, X4, X5, X6, Y1, Y2, Y3, Y4, Y5, and Y6 are all as defined for formula (I-A) above and described in classes and subclasses herein for formula (I-A), both singly and in combination.
In some embodiments, the present disclosure provides compounds, or pharmaceutically acceptable salts thereof, of formula (I-L-1) or (I-L-2):
wherein M, L, X1, X2, X3, X4, X5, X6, Y1, Y2, Y3, Y4, Y5, and Y6 are all as defined for formula (I-A) above and described in classes and subclasses herein for formula (I-A), both singly and in combination.
In some embodiments, the present disclosure provides compounds, or pharmaceutically acceptable salts thereof, of formula (I-M):
wherein M, L, X1, X2, X3, X4, X5, X6, Ra, Rb, Rc, Rd, Re, Rf, Rg, and Rh are all as defined for formula (I) and (I-A) above and described in classes and subclasses herein for formula (I) and (I-A), both singly and in combination.
In some embodiments, the present disclosure provides compounds, or pharmaceutically acceptable salts thereof, of formula (I-M-1):
wherein M, L, X1, X2, X3, X4, X5, X6, Ra, Rd, Re, Rf, Rg, and Rh are all as defined for formula (I-M) above and described in classes and subclasses herein for formula (I-M), both singly and in combination, and
In some embodiments, the present disclosure provides compounds, or pharmaceutically acceptable salts thereof, of formula (I-M-2):
wherein M, L, X1, X2, X3, X4, X5, Ra, Rd, Re, Rf, Rg, and Rh are all as defined for formula (I-M) above and described in classes and subclasses herein for formula (I-M), both singly and in combination, and
In some embodiments, the present disclosure provides compounds, or pharmaceutically acceptable salts thereof, of formula (I-M-3):
wherein M, L, X1, X2, X3, X4, X5, Ra, Rd, Re, Rf, Rg, and Rh are all as defined for formula (I-M) above and described in classes and subclasses herein for formula (I-M), both singly and in combination, and
In some embodiments, the present disclosure provides compounds, or pharmaceutically acceptable salts thereof, of formula (I-M-4):
wherein M, L, X1, X2, X3, X5, X6, Ra, Rb, Rd, Rf, Rg, and Rh are all as defined for formula (I-M) above and described in classes and subclasses herein for formula (I-M), both singly and in combination, and
In some embodiments, the disclosure relates to a compound of formula (I), (I-1), (I-2), (I-3), or (I-4), or a pharmaceutically acceptable salt thereof, wherein Ar1 is independently phenylene or 5-6 membered heteroarylene, wherein said phenylene or heteroarylene is substituted with m R1 groups. In some embodiments, Ar1 is phenylene substituted with m R1 groups. In some embodiments, Ar1 is phenylene substituted with 1-2 R1 groups selected from the group consisting of halo, cyano, hydroxyl, C1-C6 alkyl, C1-C6 alkoxy, C1-C6 haloalkyl, and C1-C6 hydroxyalkyl. In some embodiments, Ar1 is phenylene. In some embodiments, Ar1 is 5-6 membered heteroarylene substituted with m R1 groups. In some embodiments, Ar1 is 5-6 membered heteroarylene substituted with 1-2 R1 groups selected from the group consisting of halo, cyano, hydroxyl, C1-C6 alkyl, C1-C6 alkoxy, C1-C6 haloalkyl, and C1-C6 hydroxyalkyl. In some embodiments, Ar1 is 5-membered heteroarylene substituted with m R1 groups. In some embodiments, Ar1 is pyrazole. In some embodiments, Ar1 is thiazole. In some embodiments, Ar1 is 6-membered heteroarylene substituted with m R1 groups.
In some embodiments, the disclosure relates to a compound of formula (I), (I-1), (I-2), (I-3), (I-4), (I-M), (I-M-1), (I-M-2), (I-M-3), or (I-M-4), or a pharmaceutically acceptable salt thereof, wherein Ar2 is independently phenylene or 5-10 membered heteroarylene, wherein said phenylene or heteroarylene is substituted with n R2 groups. In some embodiments, Ar2 is phenylene or 5-6 membered heteroarylene, wherein said phenylene or heteroarylene is substituted with n R2 groups. In some embodiments, Ar2 is phenylene substituted with n R2 groups. In some embodiments, Ar2 is phenylene substituted with 1-2 R2 groups selected from the group consisting of halo, cyano, hydroxyl, C1-C6 alkyl, C1-C6 alkoxy, C1-C6 haloalkyl, and C1-C6 hydroxyalkyl. In some embodiments, Ar2 is phenylene. In some embodiments, Ar2 is 5-10 membered heteroarylene substituted with n R2 groups. In some embodiments, Ar2 is 5-6 membered heteroarylene substituted with n R2 groups. In some embodiments, Ar2 is 5-6 membered heteroarylene substituted with 1-2 R2 groups selected from the group consisting of halo, cyano, hydroxyl, C1-C6 alkyl, C1-C6 alkoxy, C1-C6 haloalkyl, and C1-C6 hydroxyalkyl. In some embodiments, Ar2 is 5-membered heteroarylene substituted with n R2 groups. In some embodiments, Ar2 is 6-membered heteroarylene substituted with n R2 groups. In some embodiments, Ar2 is pyridine. In some embodiments, Ar2 is 7-membered heteroarylene substituted with n R2 groups. In some embodiments, Ar2 is 8-membered heteroarylene substituted with n R2 groups. In some embodiments, Ar2 is 9-membered heteroarylene substituted with n R2 groups. In some embodiments, Ar2 is 10-membered heteroarylene substituted with n R2 groups.
In some embodiments, the disclosure relates to a compound of formula (I), (I-1), (I-2), (I-3), (I-4), (I-A), (I-A-1), (I-A-2), (I-A-3), (I-A-4), (I-B), (I-B-1), (I-B-2), (I-B-3), (I-B-4), (I-F-1), (I-F-2), (I-G-1), (I-G-2), (I-H-1), (I-H-2), (I-J-1), (I-J-2), (I-K-1), (I-K-2), (I-L-1), (I-L-2), (I-M), (I-M-1), (I-M-2), (I-M-3), or (I-M-4), or a pharmaceutically acceptable salt thereof, wherein L is —O—, —S—, —NR3—, —C(R4)2—, —S(O)2—, or —S(O)—. In some embodiments, L is —O—, —S—, or —NH—. In some embodiments, L is —O—. In some embodiments, L is —S—. In some embodiments, L is —NR3—. In some embodiments, L is —NH—. In some embodiments, L is —C(R4)2—. In some embodiments, L is —CH2—. In some embodiments, L is —S(O)2—. In some embodiments, L is —S(O)—.
In some embodiments, the disclosure relates to a compound of formula (I), (I-1), (I-2), (I-3), (I-4), (I-A), (I-A-1), (I-A-2), (I-A-3), (I-A-4), (I-B), (I-B-1), (I-B-2), (I-B-3), (I-B-4), (I-F-1), (I-F-2), (I-G-1), (I-G-2), (I-H-1), (I-H-2), (I-J-1), (I-J-2), (I-K-1), (I-K-2), (I-L-1), (I-L-2), (I-M), (I-M-1), (I-M-2), (I-M-3), or (I-M-4), or a pharmaceutically acceptable salt thereof, wherein M is C1-C6 alkyl, C1-C6 haloalkyl, 3-6 membered cycloalkyl, phenyl, or 5-6 membered heteroaryl, wherein said cycloalkyl, phenyl, or heteroaryl is substituted with p R5 groups. In some embodiments, M is 3-6 membered cycloalkyl, phenyl, or 5-6 membered heteroaryl, wherein said cycloalkyl, phenyl, or heteroaryl is substituted with p R5 groups. In some embodiments, M is C1-C6 alkyl. In some embodiments, M is C1-C6 haloalkyl. In some embodiments, M is 3-6 membered cycloalkyl substituted with p R5 groups. In some embodiments, M is 3-6 membered cycloalkyl. In some embodiments, M is 3-6 membered cycloalkyl substituted with 1-2 R5 groups selected from the group consisting of halo, cyano, hydroxyl, C1-C6 alkyl, C1-C6 haloalkyl, and C1-C6 hydroxyalkyl. In some embodiments, M is phenyl substituted with p R5 groups. In some embodiments, M is phenyl. In some embodiments, M is phenyl substituted with 1-2 R5 groups selected from the group consisting of halo, cyano, hydroxyl, C1-C6 alkyl, C1-C6 haloalkyl, C1-C6 alkoxy, and C1-C6 hydroxyalkyl. In some embodiments, M is phenyl substituted with fluoro. In some embodiments, M is 5-6 membered heteroaryl substituted with p R5 groups. In some embodiments, M is 5-6 membered heteroaryl. In some embodiments, M is 5-6 membered heteroaryl substituted with 1-2 R5 groups selected from the group consisting of halo, cyano, hydroxyl, C1-C6 alkyl, C1-C6 alkoxy, C1-C6 haloalkyl, and C1-C6 hydroxyalkyl.
In some embodiments, the disclosure relates to a compound of formula (I), (I-1), (I-2), (I-3), (I-4), (I-A), (I-A-1), (I-A-2), (I-A-3), (I-A-4), (I-B), (I-B-1), (I-B-2), (I-B-3), (I-B-4), (I-C), (I-C-1), (I-C-2), (I-C-3), (I-C-4), (I-C-a), (I-C-b), (I-C-c), (I-C-d), (I-C-e), (I-C-f), (I-F-1), (I-F-2), (I-G-1), (I-G-2), (I-H-1), (I-H-2), (I-J-1), (I-J-2), (I-K-1), (I-K-2), (I-L-1), (I-L-2), (I-M), (I-M-1), (I-M-2), (I-M-3), or (I-M-4), or a pharmaceutically acceptable salt thereof, wherein each occurrence of R1, R2, and R5 is independently halo, cyano, NO2, oxo, hydroxyl, —R6, —OR6, C1-C6 alkyl, C1-C6 haloalkyl, C1-C6 hydroxyalkyl, —C1-C6 alkylene-R6, C1-C6 alkoxy, C1-C6 haloalkoxy, —C0-C3 alkylene-NR6R7, —C0-C3 alkylene-NR7R8, —C0-C3 alkylene-C(O)NR6R7, —C0-C3 alkylene-C(O)NR7R8, —C0-C3 alkylene-NR7C(O)R6, —C0-C3 alkylene-NR7C(O)R8, —C0-C3 alkylene-NR7S(O)2R6, —C0-C3 alkylene-C(O)R6, —C0-C3 alkylene-C(O)R7, —C0-C3 alkylene-SR6, —C0-C3 alkylene-S(O)R6, —C0-C3 alkylene-S(O)2R6, —C0-C3 alkylene-S(O)2R7, —C0-C3 alkylene-S(O)2NR6R7, —C0-C3 alkylene-S(O)2NR7R8, —C0-C3 alkylene-NR7C(O)NR8R9, —C0-C3 alkylene- NR7S(O)2NR8R9, —C0-C3 alkylene-C(O)OR7, —C0-C3 alkylene-C(O)OR6, —C0-C3 alkylene-OC(O)R7, —C0-C3 alkylene-OC(O)R6, —C0-C3 alkylene-NR7C(O)OR8, or —C0-C3 alkylene-NR7S(O)2R8. In some embodiments, each occurrence of R1 is independently halo, cyano, hydroxyl, C1-C6 alkyl, C1-C6 alkoxy, C1-C6 haloalkyl, and C1-C6 hydroxyalkyl. In some embodiments, each occurrence of R1 is independently halo (e.g., fluoro, chloro, bromo, or iodo). In some embodiments, each occurrence of R1 is fluoro. In some embodiments, each occurrence of R1 is cyano. In some embodiments, each occurrence of R1 is hydroxyl. In some embodiments, each occurrence of R1 is C1-C6 alkyl. In some embodiments, each occurrence of R1 is C1-C6 alkoxy. In some embodiments, each occurrence of R1 is C1-C6 haloalkyl. In some embodiments, each occurrence of R1 is C1-C6 hydroxyalkyl. In some embodiments, each occurrence of R2 is independently halo, cyano, hydroxyl, C1-C6 alkyl, C1-C6 alkoxy, C1-C6 haloalkyl, and C1-C6 hydroxyalkyl. In some embodiments, each occurrence of R2 is independently halo (e.g., fluoro, chloro, bromo, or iodo). In some embodiments, each occurrence of R2 is fluoro. In some embodiments, each occurrence of R2 is cyano. In some embodiments, each occurrence of R2 is hydroxyl. In some embodiments, each occurrence of R2 is C1-C6 alkyl. In some embodiments, each occurrence of R2 is C1-C6 alkoxy. In some embodiments, each occurrence of R2 is C1-C6 haloalkyl. In some embodiments, each occurrence of R2 is C1-C6 hydroxyalkyl. In some embodiments, each occurrence of R5 is independently halo, cyano, hydroxyl, C1-C6 alkyl, C1-C6 alkoxy, C1-C6 haloalkyl, and C1-C6 hydroxyalkyl. In some embodiments, each occurrence of R5 is independently halo (e.g., fluoro, chloro, bromo, or iodo). In some embodiments, each occurrence of R5 is fluoro. In some embodiments, each occurrence of R5 is cyano. In some embodiments, each occurrence of R5 is hydroxyl. In some embodiments, each occurrence of R5 is C1-C6 alkyl. In some embodiments, each occurrence of R5 is C1-C6 alkoxy. In some embodiments, each occurrence of R5 is C1-C6 haloalkyl. In some embodiments, each occurrence of R5 is C1-C6 hydroxyalkyl.
In some embodiments, the disclosure relates to a compound of formula (I), (I-1), (I-2), (I-3), (I-4), (I-A), (I-A-1), (I-A-2), (I-A-3), (I-A-4), (I-B), (I-B-1), (I-B-2), (I-B-3), (I-B-4), (I-F-1), (I-F-2), (I-G-1), (I-G-2), (I-H-1), (I-H-2), (I-J-1), (I-J-2), (I-K-1), (I-K-2), (I-L-1), (I-L-2), (I-M), (I-M-1), (I-M-2), (I-M-3), or (I-M-4), or a pharmaceutically acceptable salt thereof, wherein R3 is H, C1-C6 alkyl, or C1-C6 haloalkyl. In some embodiments, R3 is H. In some embodiments, R3 is C1-C6 alkyl. In some embodiments, R3 is C1-C6 haloalkyl.
In some embodiments, the disclosure relates to a compound of formula (I), (I-1), (I-2), (I-3), (I-4), (I-A), (I-A-1), (I-A-2), (I-A-3), (I-A-4), (I-B), (I-B-1), (I-B-2), (I-B-3), (I-B-4), (I-F-1), (I-F-2), (I-G-1), (I-G-2), (I-H-1), (I-H-2), (I-J-1), (I-J-2), (I-K-1), (I-K-2), (I-L-1), (I-L-2), (I-M), (I-M-1), (I-M-2), (I-M-3), or (I-M-4), or a pharmaceutically acceptable salt thereof, wherein each R4 is independently H, C1-C6 alkyl, or C1-C6 haloalkyl, or two R4 groups together with the carbon atom to which they are attached form a 3-6 membered cycloalkyl or heterocycloalkyl. In some embodiments, each R4 is H. In some embodiments, two R4 groups together with the carbon atom to which they are attached form a 3-6 membered cycloalkyl. In some embodiments, two R4 groups together with the carbon atom to which they are attached form a 3-6 membered heterocycloalkyl.
In some embodiments, the disclosure relates to a compound of formula (I), (I-1), (I-2), (I-3), (I-4), (I-A), (I-A-1), (I-A-2), (I-A-3), (I-A-4), (I-B), (I-B-1), (I-B-2), (I-B-3), (I-B-4), (I-C), (I-C-1), (I-C-2), (I-C-3), (I-C-4), (I-C-a), (I-C-b), (I-C-c), (I-C-d), (I-C-e), (I-C-f), (I-F-2), (I-G-1), (I-G-2), (I-H-1), (I-H-2), (I-J-1), (I-J-2), (I-K-1), (I-K-2), (I-L-1), (I-L-2), (I-M), (I-M-1), (I-M-2), (I-M-3), or (I-M-4), or a pharmaceutically acceptable salt thereof, wherein each R6 is 5-10 membered heteroaryl, 4-10 membered heterocycloalkyl, 6-10 membered aryl, or 3-8 membered cycloalkyl, wherein said heteroaryl, heterocycloalkyl, aryl, or cycloalkyl is optionally substituted with 1-5 substituents independently selected from the group consisting of halo, oxo, C1-C6 alkyl, C1-C6 haloalkyl, C1-C6 hydroxyalkyl, C1-C6 alkoxy, C1-C6 haloalkoxy, C2-C6 alkenyl, C2-C6 alkynyl, 5-10 membered heteroaryl, 4-10 membered heterocycloalkyl, 6-10 membered aryl, 3-8 membered cycloalkyl, —NR10C(O)NR11R12, —NR10R11, —C(O)R10, —NR10C(O)R11, —NR10C(O)OR11, —S(O)2R10, —C(O)NR10R11, —C(O)OR10, —S(O)2NR10R11, —NR10S(O)2R11, —OR10, —OC(O)R10, —OS(O)2R10, —OC(O)NR10R11, —OC(O)OR10, —OS(O)2NR10R11, —C(O)NR10C(O)NR11R12, —C(O)C(O)R10, —C(O)NR10C(O)R11, —C(O)NR10C(O)OR11, —C(O)S(O)2R10, —C(O)C(O)NR10R11, —C(O)C(O)OR10, —C(O)S(O)2NR10R11, —C(O)NR10S(O)2R11, —C1-C6 alkylene-R10, —C1-C6 alkylene-NR10C(O)NR11R12, —C1-C6 alkylene-NR10R11, —C1-C6 alkylene-C(O)R10, —C1-C6 alkylene-NR10C(O)R11, —C1-C6 alkylene-NR10C(O)OR11, —C1-C6 alkylene-S(O)2R19, —C1-C6 alkylene-C(O)NR10R11, —C1-C6 alkylene-C(O)OR10, —C1-C6 alkylene-S(O)2NR10R11, —C1-C6 alkylene-NR10S(O)2R11, —C1-C6 alkenylene-R10, —C1-C6 alkenylene-NR10C(O)NR11R12, —C1-C6 alkenylene-NR10R11, —C1-C6 alkenylene-C(O)R10, —C1-C6 alkenylene-NR10C(O)R11, —C1-C6 alkenylene-NR10C(O)OR11, —C1-C6 alkenylene-S(O)2R10, —C1-C6 alkenylene-C(O)NR10R11, —C1-C6 alkenylene-C(O)OR10, —C1-C6 alkenylene-S(O)2NR10R11, and —C1-C6 alkenylene-NR19S(O)2R11. In some embodiments, each R6 is independently optionally substituted 5-10 membered heteroaryl. In some embodiments, each R6 is independently optionally substituted 4-10 membered heterocycloalkyl. In some embodiments, each R6 is independently optionally substituted 6-10 membered aryl. In some embodiments, each R6 is independently optionally substituted 3-8 membered cycloalkyl.
In some embodiments, the disclosure relates to a compound of formula (I), (I-1), (I-2), (I-3), (I-4), (I-A), (I-A-1), (I-A-2), (I-A-3), (I-A-4), (I-B), (I-B-1), (I-B-2), (I-B-3), (I-B-4), (I-C), (I-C-1), (I-C-2), (I-C-3), (I-C-4), (I-C-a), (I-C-b), (I-C-c), (I-C-d), (I-C-e), (I-C-f), (I-F-1), (I-F-2), (I-G-1), (I-G-2), (I-H-1), (I-H-2), (I-J-1), (I-J-2), (I-K-1), (I-K-2), (I-L-1), (I-L-2), (I-M), (I-M-1), (I-M-2), (I-M-3), or (I-M-4), or a pharmaceutically acceptable salt thereof, wherein each R7, R8, and R9 is independently hydrogen or C1-C6 alkyl. In some embodiments, each R7, R8, and R9 is independently hydrogen.
In some embodiments, the disclosure relates to a compound of formula (I), (I-1), (I-2), (I-3), (I-4), (I-A), (I-A-1), (I-A-2), (I-A-3), (I-A-4), (I-B), (I-B-1), (I-B-2), (I-B-3), (I-B-4), (I-C), (I-C-1), (I-C-2), (I-C-3), (I-C-4), (I-C-a), (I-C-b), (I-C-c), (I-C-d), (I-C-e), (I-C-f), (I-F-1), (I-F-2), (I-G-1), (I-G-2), (I-H-1), (I-H-2), (I-J-1), (I-J-2), (I-K-1), (I-K-2), (I-L-1), (I-L-2), (I-M), (I-M-1), (I-M-2), (I-M-3), or (I-M-4), or a pharmaceutically acceptable salt thereof, wherein each R10, R11, and R12 is independently hydrogen, C1-C6 alkyl, 5-10 membered heteroaryl, 4-10 membered heterocycloalkyl, 6-10 membered aryl, or 3-8 membered cycloalkyl. In some embodiments, each R1-9, RH, and R12 is independently hydrogen.
In some embodiments, the disclosure relates to a compound of formula (I), (I-1), (I-2), (I-3), or (I-4), or a pharmaceutically acceptable salt thereof, wherein m is 0-4 (i.e., m is 0, 1, 2, 3, or 4). In some embodiments, m is 0. In some embodiments, m is 1. In some embodiments, m is 2. In some embodiments, m is 3. In some embodiments, in is 4. In some embodiments, in is 0, 1, or 2. In some embodiments, m is 1 or 2.
In some embodiments, the disclosure relates to a compound of formula (I), (I-1), (I-2), (I-3), (I-4), (I-C), (I-C-1), (I-C-2), (I-C-3), (I-C-4), (I-C-a), (I-C-b), (I-C-c), (I-C-d), (I-C-e), (I-C-f), (I-M), (I-M-1), (I-M-2), (I-M-3), or (I-M-4), or a pharmaceutically acceptable salt thereof, wherein n is 0-4 (i.e., n is 0, 1, 2, 3, or 4). In some embodiments, n is 0. In some embodiments, n is 1. In some embodiments, n is 2. In some embodiments, n is 3. In some embodiments, n is 4. In some embodiments, n is 0, 1, or 2. In some embodiments, n is 1 or 2.
In some embodiments, the disclosure relates to a compound of formula (I), (I-1), (I-2), (I-3), (I-4), (I-A), (I-A-1), (I-A-2), (I-A-3), (I-A-4), (I-B), (I-B-1), (I-B-2), (I-B-3), (I-B-4), (I-C), (I-C-1), (I-C-2), (I-C-3), (I-C-4), (I-C-a), (I-C-b), (I-C-c), (I-C-d), (I-C-e), (I-C-f), (I-F-1), (I-F-2), (I-G-1), (I-G-2), (I-H-1), (I-H-2), (I-J-1), (I-J-2), (I-K-1), (I-K-2), (I-L-1), (I-L-2), (I-M), (I-M-1), (I-M-2), (I-M-3), or (I-M-4), or a pharmaceutically acceptable salt thereof, wherein p is 0-4 (i.e., p is 0, 1, 2, 3, or 4). In some embodiments, p is 0. In some embodiments, p is 1. In some embodiments, p is 2. In some embodiments, p is 3. In some embodiments, p is 4. In some embodiments, p is 0, 1, or 2. In some embodiments, p is 1 or 2. In some embodiments, n and p are both 0. In some embodiments, m and n are both 0. In some embodiments, m and n are both 0. In some embodiments, m, n, and p are 0. In some embodiments, in and n are 0, and p is 1.
In some embodiments, the disclosure relates to a compound of formula (I), (I-A), (I-B), (I-C), (I-D), (I-E), or (I-M), or a pharmaceutically acceptable salt thereof, wherein Ra and Rb form a C1-C4 alkylene group between the atoms to which they are attached, wherein said C1-C4 alkylene group is substituted with 0-4 substituents selected from the group consisting of halogen, C1-C3 alkyl, and C1-C3 haloalkyl. In some embodiments, Ra and Rb form a C1-C4 alkylene group between the atoms to which they are attached; and Rc, Rd, Re, Rf, Rg, and Rh are each hydrogen. In some embodiments, Ra and Rb form a C1 alkylene group between the atoms to which they are attached; and Rc, Rd, Re, Rf, Rg, and Rh are each hydrogen. In some embodiments, Ra and Rb form a C2 alkylene group between the atoms to which they are attached; and Rc, Rd, Re, Rf, Rg, and Rh are each hydrogen. In some embodiments, Ra and Rb form a C3 alkylene group between the atoms to which they are attached; and Rc, Rd, Re, Rf, Rg, and Rh are each hydrogen. In some embodiments, Ra and Rb form a C4 alkylene group between the atoms to which they are attached; and Rc, Rd, Re, Rf, Rg, and Rh are each hydrogen.
In some embodiments, the disclosure relates to a compound of formula (I), (I-A), (I-B), (I-C), (I-D), (I-E), or (I-M), or a pharmaceutically acceptable salt thereof, wherein Ra and Re form a C1-C2 alkylene group between the atoms to which they are attached, wherein said C1-C2 alkylene group is substituted with 0-4 substituents selected from the group consisting of halogen, C1-C3 alkyl, and C1-C3 haloalkyl. In some embodiments, Ra and Re form a C1-C2 alkylene group between the atoms to which they are attached; and Rb, Rc, Rd, Rf, Rg, and Rh are each hydrogen. In some embodiments, Ra and Re form a C1 alkylene group between the atoms to which they are attached; and Rb, Rc, Rd, Rf, Rg, and Rh are each hydrogen. In some embodiments, Ra and Re form a C2 alkylene group between the atoms to which they are attached; and Rb, Rc, Rd, Rf, Rg, and Rh are each hydrogen.
In some embodiments, the disclosure relates to a compound of formula (I), (I-A), (I-B), (I-C), (I-D), (I-E), or (I-M), or a pharmaceutically acceptable salt thereof, wherein Ra and Rg form a C1-C3 alkylene group between the atoms to which they are attached, wherein said C1-C3 alkylene group is substituted with 0-4 substituents selected from the group consisting of halogen, C1-C3 alkyl, and C1-C3 haloalkyl. In some embodiments, Ra and Rg form a C1-C3 alkylene group between the atoms to which they are attached; and Rb, Rc, Rd, Re, Rf, and Rh are each hydrogen. In some embodiments, Ra and Rg form a C1 alkylene group between the atoms to which they are attached; and Rb, Rc, Rd, Re, Rf, and Rh are each hydrogen. In some embodiments, Ra and Rg form a C2 alkylene group between the atoms to which they are attached; and Rb, Rc, Rd, Re, Rf, and Rh are each hydrogen. In some embodiments, Ra and Rg form a C3 alkylene group between the atoms to which they are attached; and Rb, Rc, Rd, Re, Rf, and Rh are each hydrogen.
In some embodiments, the disclosure relates to a compound of formula (I), (I-A), (I-B), (I-C), (I-D), (I-E), or (I-M), or a pharmaceutically acceptable salt thereof, wherein Rb and Rc form a C1-C4 alkylene group between the atoms to which they are attached, wherein said C1-C4 alkylene group is substituted with 0-4 substituents selected from the group consisting of halogen, C1-C3 alkyl, and C1-C3 haloalkyl. In some embodiments, Rb and Rc form a C1-C4 alkylene group between the atoms to which they are attached; and Ra, Rd, Re, Rf, Rg, and Rh are each hydrogen.
In some embodiments, Rb and Rc form a C1-C3 alkylene group between the atoms to which they are attached; and Ra, Rd, Re, Rf, Rg, and Rh are each hydrogen. In some embodiments, Rb and Rc form a C1 alkylene group between the atoms to which they are attached; and Ra, Rd, Re, Rf, Rg, and Rh are each hydrogen. In some embodiments, Rb and Rc form a C2 alkylene group between the atoms to which they are attached; and Ra, Rd, Re, Rf, Rg, and Rh are each hydrogen. In some embodiments, Rb and Rc form a C3 alkylene group between the atoms to which they are attached; and Ra, Rd, Re, Rf, Rg, and Rh are each hydrogen. In some embodiments, Rb and Rc form a C4 alkylene group between the atoms to which they are attached; and Ra, Rd, Re, Rf, Rg, and Rh are each hydrogen.
In some embodiments, the disclosure relates to a compound of formula (I), (I-A), (I-B), (I-C), (I-D), (I-E), or (I-M), or a pharmaceutically acceptable salt thereof, wherein Rb and Re form a C1-C3 alkylene group between the atoms to which they are attached, wherein said C1-C3 alkylene group is substituted with 0-4 substituents selected from the group consisting of halogen, C1-C3 alkyl, and C1-C3 haloalkyl. In some embodiments, Rb and Re form a C1-C3 alkylene group between the atoms to which they are attached; and Ra, Rc, Rd, Rf, Rg, and Rh are each hydrogen. In some embodiments, Rb and Re form a C1 alkylene group between the atoms to which they are attached; and Ra, Rc, Rd, Rf, Rg, and Rh are each hydrogen. In some embodiments, Rb and Re form a C2 alkylene group between the atoms to which they are attached; and Ra, Rc, Rd, Rf, Rg, and Rh are each hydrogen. In some embodiments, Rb and Re form a C3 alkylene group between the atoms to which they are attached; and Ra, Rc, Rd, Rf, Rg, and Rh are each hydrogen.
In some embodiments, the disclosure relates to a compound of formula (I), (I-A), (I-B), (I-C), (I-D), (I-E), or (I-M), or a pharmaceutically acceptable salt thereof, wherein Rb and Rg form a C1-C4 alkylene group between the atoms to which they are attached, wherein said C1-C4 alkylene group is substituted with 0-4 substituents selected from the group consisting of halogen, C1-C3 alkyl, and C1-C3 haloalkyl. In some embodiments, Rb and Rg form a C1-C4 alkylene group between the atoms to which they are attached; and Ra, Rc, Rd, Re, Rf, and Rh are each hydrogen. In some embodiments, Rb and Rg form a C1 alkylene group between the atoms to which they are attached; and Ra, Rc, Rd, Re, Rf, and Rh are each hydrogen. In some embodiments, Rb and Rg form a C2 alkylene group between the atoms to which they are attached; and Ra, Rc, Rd, Re, Rf, and Rh are each hydrogen. In some embodiments, Rb and Rg form a C3 alkylene group between the atoms to which they are attached; and Ra, Rc, Rd, Re, Rf, and Rh are each hydrogen. In some embodiments, Rb and Rg form a C4 alkylene group between the atoms to which they are attached; and Ra, Rc, Rd, Re, Rf, and Rh are each hydrogen.
In some embodiments, the disclosure relates to a compound of formula (I), (I-A), (I-B), (I-C), (I-D), (I-E), or (I-M), or a pharmaceutically acceptable salt thereof, wherein Rc and Rd together with the atom to which they are attached, form a 3-6 membered cycloalkyl or heterocycloalkyl, wherein said 3-6 membered cycloalkyl or heterocycloalkyl is substituted with 0-4 substituents selected from the group consisting of halogen, C1-C3 alkyl, and C1-C3 haloalkyl. In some embodiments, Rc and Rd together with the atom to which they are attached, form a 3-6 membered cycloalkyl or heterocycloalkyl; and Ra, Rb, Re, Rf, Rg, and Rh are each hydrogen. In some embodiments, Rc and Rd together with the atom to which they are attached, form a 3 membered cycloalkyl or a 4 membered heterocycloalkyl; and Ra, Rb, Re, Rf, Rg, and Rh are each hydrogen. In some embodiments, Rc and Rd together with the atom to which they are attached, form a 3-6 membered cycloalkyl; and Ra, Rb, Re, Rf, Rg, and Rh are each hydrogen. In some embodiments, Rc and Rd together with the atom to which they are attached, form a 3 membered cycloalkyl; and Ra, Rb, Re, Rf, Rg and Rh are each hydrogen. In some embodiments, Rc and Rd together with the atom to which they are attached, form a 4 membered cycloalkyl; and Ra, Rb, Re, Rf, Rg, and Rh are each hydrogen. In some embodiments, Rc and Rd together with the atom to which they are attached, form a 5 membered cycloalkyl; and Ra, Rb, Re, Rf, Rg, and Rh are each hydrogen. In some embodiments, Rc and Rd together with the atom to which they are attached, form a 6 membered cycloalkyl; and Ra, Rb, Re, Rf, Rg, and Rh are each hydrogen. In some embodiments, Rc and Rd together with the atom to which they are attached, form a 3-6 membered heterocycloalkyl ring; and Ra, Rb, Re, Rf, Rg, and Rh are each hydrogen. In some embodiments, Rc and Rd together with the atom to which they are attached, form a 3-6 membered heterocycloalkyl ring, wherein the 3-6 membered heterocycloalkyl ring contains O, S, or NH; and Ra, Rb, Re, Rf, Rg, and Rh are each hydrogen. In some embodiments, Rc and Rd together with the atom to which they are attached, form a 3 membered heterocycloalkyl ring; and Ra, Rb, Re, Rf, Rg, and Rh are each hydrogen. In some embodiments, Rc and Rd together with the atom to which they are attached, form a 4 membered heterocycloalkyl ring; and Ra, Rb, Re, Rf, Rg, and Rh are each hydrogen. In some embodiments, Rc and Rd together with the atom to which they are attached, form an oxetane ring; and Ra, Rb, Re, Rf, Rg, and Rh are each hydrogen. In some embodiments, Rc and Rd together with the atom to which they are attached, form a 5 membered heterocycloalkyl ring; and Ra, Rb, Re, Rf, Rg, and Rh are each hydrogen. In some embodiments, Rc and Rd together with the atom to which they are attached, form a 6 membered heterocycloalkyl ring; and Ra, Rb, Re, Rf, Rg, and Rh are each hydrogen. In some embodiments, Rc and Rd together form ═O. In some embodiments, Rc and Rd together form ═O; and Ra, Rb, Re, Rf, Rg, and Rh are each hydrogen.
In some embodiments, the disclosure relates to a compound of formula (I), (I-A), (I-B), (I-C), (I-D), (I-E), or (I-M), or a pharmaceutically acceptable salt thereof, wherein Rc and Re form a C1-C4 alkylene group between the atoms to which they are attached, wherein said C1-C4 alkylene group is substituted with 0-4 substituents selected from the group consisting of halogen, C1-C3 alkyl, and C1-C3 haloalkyl. In some embodiments, Rc and Re form a C1-C4 alkylene group between the atoms to which they are attached; and Ra, Rb, Rd, Rf, Rg, and Rh are each hydrogen. In some embodiments, Rc and Re form a C1 alkylene group between the atoms to which they are attached; and Ra, Rb, Rd, Rf, Rg, and Rh are each hydrogen. In some embodiments, Rc and Re form a C2 alkylene group between the atoms to which they are attached; and Ra, Rb, Rd, Rf, Rg, and Rh are each hydrogen. In some embodiments, Rc and Re form a C3 alkylene group between the atoms to which they are attached; and Ra, Rb, Rd, Rf, Rg, and Rh are each hydrogen. In some embodiments, Rc and Re form a C4 alkylene group between the atoms to which they are attached; and Ra, Rb, Rd, Rf, Rg, and Rh are each hydrogen.
In some embodiments, the disclosure relates to a compound of formula (I), (I-A), (I-B), (I-C), (I-D), (I-E), or (I-M), or a pharmaceutically acceptable salt thereof, wherein Rc and Rg form a C1-C3 alkylene group between the atoms to which they are attached, wherein said C1-C3 alkylene group is substituted with 0-4 substituents selected from the group consisting of halogen, C1-C3 alkyl, and C1-C3 haloalkyl. In some embodiments, Rc and Rg form a C1-C3 alkylene group between the atoms to which they are attached; and Ra, Rb, Rd, Re, Rf, and Rh are each hydrogen. In some embodiments, Rc and Rg form a C1-C2 alkylene group between the atoms to which they are attached; and Ra, Rb, Rd, Re, Rf, and Rh are each hydrogen. In some embodiments, Rc and Rg form a C1 alkylene group between the atoms to which they are attached; and Ra, Rb, Rd, Re, Rf, and Rh are each hydrogen. In some embodiments, Rc and Rg form a C2 alkylene group between the atoms to which they are attached; and Ra, Rb, Rd, Re, Rf, and Rh are each hydrogen. In some embodiments, Rc and Rg form a C3 alkylene group between the atoms to which they are attached; and Ra, Rb, Rd, Re, Rf, and Rh are each hydrogen.
In some embodiments, the disclosure relates to a compound of formula (I), (I-A), (I-B), (I-C), (I-D), (I-E), or (I-M), or a pharmaceutically acceptable salt thereof, wherein Re and Rf together with the atom to which they are attached, form a 3-6 membered cycloalkyl or heterocycloalkyl, wherein said 3-6 membered cycloalkyl or heterocycloalkyl is substituted with 0-4 substituents selected from the group consisting of halogen, C1-C3 alkyl, and C1-C3 haloalkyl. In some embodiments, Rc and Rf together with the atom to which they are attached, form a 3-6 membered cycloalkyl or heterocycloalkyl; and Ra, Rb, Rc, Rd, Rg, and Rh are each hydrogen. In some embodiments, Re and Rf together with the atom to which they are attached, form a 3-6 membered cycloalkyl; and Ra, Rb, Rc, Rd, Rg, and Rh are each hydrogen. In some embodiments, Re and Rf together with the atom to which they are attached, form a 3 membered cycloalkyl; and Ra, Rb, Rc, Rd, Rg, and Rh are each hydrogen. In some embodiments, Re and Rf together with the atom to which they are attached, form a 4 membered cycloalkyl; and Ra, Rb, Re, Rd, Rg, and Rh are each hydrogen. In some embodiments, Re and Rf together with the atom to which they are attached, form a 5 membered cycloalkyl; and Ra, Rb, Rc, Rd, Rg, and Rh are each hydrogen. In some embodiments, Re and Rf together with the atom to which they are attached, form a 6 membered cycloalkyl; and Ra, Rb, Rc, Rd, Rg, and Rh are each hydrogen. In some embodiments, Re and Rf together with the atom to which they are attached, form a 3-6 membered heterocycloalkyl ring; and Ra, Rb, Rc, Rd, Rg, and Rh are each hydrogen. In some embodiments, Re and Rf together with the atom to which they are attached, form a 3-6 membered heterocycloalkyl ring, wherein the 3-6 membered heterocycloalkyl ring contains O, S, or NH; and Ra, Rb, Rc, Rd, Rg, and Rh are each hydrogen. In some embodiments, Re and Rf together with the atom to which they are attached, form a 3 membered heterocycloalkyl ring; and Ra, Rb, Rc, Rd, Rg, and Rh are each hydrogen. In some embodiments, Re and Rf together with the atom to which they are attached, form a 4 membered heterocycloalkyl ring; and Ra, Rb, Rc, Rd, Rg, and Rh are each hydrogen. In some embodiments, Re and Rf together with the atom to which they are attached, form an oxetane ring; and Ra, Rb, Rc, Rd, Rg, and Rh are each hydrogen. In some embodiments, Re and Rf together with the atom to which they are attached, form a 5 membered heterocycloalkyl ring; and Ra, Rb, Rc, Rd, Rg, and Rh are each hydrogen. In some embodiments, Re and Rf together with the atom to which they are attached, form a 6 membered heterocycloalkyl ring; and Ra, Rb, Rc, Rd, Rg, and Rh are each hydrogen. In some embodiments, Re and Rf together form ═O. In some embodiments, Re and Rf together form ═O; and Ra, Rb, Rc, Rd, Rg, and Rh are each hydrogen.
In some embodiments, the disclosure relates to a compound of formula (I), (I-A), (I-B), (I-C), (I-D), (I-E), or (I-M), or a pharmaceutically acceptable salt thereof, wherein Re and Rg form a C1-C3 alkylene group between the atoms to which they are attached, wherein said C1-C3 alkylene group is substituted with 0-4 substituents selected from the group consisting of halogen, C1-C3 alkyl, and C1-C3 haloalkyl. In some embodiments, Re and Rg form a C1-C3 alkylene group between the atoms to which they are attached; and Ra, Rb, Rc, Rd, Rf, and Rh are each hydrogen. In some embodiments, Re and Rg form a C1 alkylene group between the atoms to which they are attached; and Ra, Rb, Rc, Rd, Rf, and Rh are each hydrogen. In some embodiments, Re and Rg form a C2 alkylene group between the atoms to which they are attached; and Ra, Rb, Rc, Rd, Rf, and Rh are each hydrogen. In some embodiments, Re and Rg form a C3 alkylene group between the atoms to which they are attached; and Ra, Rb, Rc, Rd, Rf, and Rh are each hydrogen.
In some embodiments, the disclosure relates to a compound of formula (I), (I-A), (I-B), (I-C), (I-D), (I-E), or (I-M), or a pharmaceutically acceptable salt thereof, wherein Rg and Rh together with the atom to which they are attached, form a 3-6 membered cycloalkyl or heterocycloalkyl, wherein said 3-6 membered cycloalkyl or heterocycloalkyl is substituted with 0-4 substituents selected from the group consisting of halogen, C1-C3 alkyl, and C1-C3 haloalkyl. In some embodiments, Rg and Rh together with the atom to which they are attached, form a 3-6 membered cycloalkyl or heterocycloalkyl; and Ra, Rb, Rc, Rd, Re, and Rf are each hydrogen. In some embodiments, Rg and Rh together with the atom to which they are attached, form a 3-6 membered cycloalkyl; and Ra, Rb, Rc, Rd, Re, and Rf are each hydrogen. In some embodiments, Rg and Rh together with the atom to which they are attached, form a 3 membered cycloalkyl; and Ra, Rb, Rc, Rd, Re, and Rf are each hydrogen. In some embodiments, Rg and Rh together with the atom to which they are attached, form a 4 membered cycloalkyl; and Ra, Rb, Rc, Rd, Re, and Rf are each hydrogen. In some embodiments, Rg and Rh together with the atom to which they are attached, form a 5 membered cycloalkyl; and Ra, Rb, Rc, Rd, Re, and Rf are each hydrogen. In some embodiments, Rg and Rh together with the atom to which they are attached, form a 6 membered cycloalkyl; and Ra, Rb, Rc, Rd, Re, and Rf are each hydrogen. In some embodiments, Rg and Rh together with the atom to which they are attached, form a 3-6 membered heterocycloalkyl ring; and Ra, Rb, Re, Rd, Re, and Rf are each hydrogen. In some embodiments, Rg and Rh together with the atom to which they are attached, form a 3-6 membered heterocycloalkyl ring, wherein the 3-6 membered heterocycloalkyl ring contains O, S, or NH; and Ra, Rb, Rc, Rd, Re, and Rf are each hydrogen. In some embodiments, Rg and Rh together with the atom to which they are attached, form a 3 membered heterocycloalkyl ring; and Ra, Rb, Re, Rd, Re, and Rf are each hydrogen. In some embodiments, Rg and Rh together with the atom to which they are attached, form a 4 membered heterocycloalkyl ring; and Ra, Rb, Rc, Rd, Re, and Rf are each hydrogen. In some embodiments, Rg and Rh together with the atom to which they are attached, form an oxetane ring; and Ra, Rb, Rc, Rd, Re, and Rf are each hydrogen. In some embodiments, Rg and Rh together with the atom to which they are attached, form a 5 membered heterocycloalkyl ring; and Ra, Rb, Rc, Rd, Re, and Rf are each hydrogen. In some embodiments, Rg and Rh together with the atom to which they are attached, form a 6 membered heterocycloalkyl ring; and Ra, Rb, Rc, Rd, Re, and Rf are each hydrogen. In some embodiments, Rg and Rh together form ═O. In some embodiments, Rg and Rh together form ═O; and Ra, Rb, Rc, Rd, Re, and Rf are each hydrogen.
In some embodiments, the disclosure relates to a compound of formula (I), (I-A), (I-B), (I-C), (I-D), (I-E), or (I-M), or a pharmaceutically acceptable salt thereof, wherein Ra, Rb, Rc, Rd, Re, Rf, Rg, and Rh are defined as follows:
(ii) Ra and Re form a C1-C2 alkylene group between the atoms to which they are attached, wherein said C1-C2 alkylene group is substituted with 0-4 substituents selected from the group consisting of halogen, C1-C3 alkyl, and C1-C3 haloalkyl; and Rb, Rc, Rd, Rf, Rg, and Rh are each independently hydrogen, halogen, C1-C3 alkyl, or C1-C3 haloalkyl; or
(iv) Rb and Rc form a C1-C4 alkylene group between the atoms to which they are attached, wherein said C1-C4 alkylene group is substituted with 0-4 substituents selected from the group consisting of halogen, C1-C3 alkyl, and C1-C3 haloalkyl; and Ra, Rd, Re, Rf, Rg, and Rh are each independently hydrogen, halogen, C1-C3 alkyl, or C1-C3 haloalkyl; or
(vii) Rc and Rd together with the atom to which they are attached, form a 3-6 membered cycloalkyl or heterocycloalkyl, wherein said 3-6 membered cycloalkyl or heterocycloalkyl is substituted with 0-4 substituents selected from the group consisting of halogen, C1-C3 alkyl, and C1-C3 haloalkyl; and Ra, Rb, Re, Rf, Rg, and Rh are each independently hydrogen, halogen, C1-C3 alkyl, or C1-C3 haloalkyl; or
(viii) Re and Rd together form ═O; and Ra, Rb, Re, Rf, Rg, and Rh are each independently hydrogen, halogen, C1-C3 alkyl, or C1-C3 haloalkyl; or
(ix) Rc and Re form a C1-C4 alkylene group between the atoms to which they are attached, wherein said C1-C4 alkylene group is substituted with 0-4 substituents selected from the group consisting of halogen, C1-C3 alkyl, and C1-C3 haloalkyl, and Ra, Rb, Rd, Rf, Rg, and Rh are each independently hydrogen, halogen, C1-C3 alkyl, or C1-C3 haloalkyl; or
(x) Rc and Rg form a C1-C3 alkylene group between the atoms to which they are attached, wherein said C1-C3 alkylene group is substituted with 0-4 substituents selected from the group consisting of halogen, C1-C3 alkyl, and C1-C3 haloalkyl, and Ra, Rb, Rd, Re, Rf, and Rh are each independently hydrogen, halogen, C1-C3 alkyl, or C1-C3 haloalkyl; or
(xi) Re and Rf together with the atom to which they are attached, form a 3-6 membered cycloalkyl or heterocycloalkyl, wherein said 3-6 membered cycloalkyl or heterocycloalkyl is substituted with 0-4 substituents selected from the group consisting of halogen, C1-C3 alkyl, and C1-C3 haloalkyl; and Ra, Rb, Rc, Rd, Rg, and Rh are each independently hydrogen, halogen, C1-C3 alkyl, or C1-C3 haloalkyl; or
(xiii) Rc and Rg form a C1-C3 alkylene group between the atoms to which they are attached, wherein said C1-C3 alkylene group is substituted with 0-4 substituents selected from the group consisting of halogen, C1-C3 alkyl, and C1-C3 haloalkyl; and Ra, Rb, Rc, Rd, Rf, and Rh are each independently hydrogen, halogen, C1-C3 alkyl, or C1-C3 haloalkyl; or
(xv) Rg and Rh together form ═O; and Ra, Rb, Rc, Rd, Re, and Rf are each independently hydrogen, halogen, C1-C3 alkyl, or C1-C3 haloalkyl.
In some embodiments, the disclosure relates to a compound of formula (I), (I-A), (I-B), (I-C), (I-D), (I-E), or (I-M), or a pharmaceutically acceptable salt thereof, wherein Ra, Rb, Rc, Rd, Re, Rf, Rg, and Rh are defined as follows:
(ii) Ra and Re form a C1-C2 alkylene group between the atoms to which they are attached; and Rb, Rc, Rd, Rf, Rg, and Rh are each hydrogen; or
(iv) Rb and Rc form a C1-C4 alkylene group between the atoms to which they are attached; and Ra, Rd, Re, Rf, Rg, and Rh are each hydrogen; or
(vii) Rc and Rd together with the atom to which they are attached, form a 3-6 membered cycloalkyl or heterocycloalkyl; and Ra, Rb, Re, Rf, Rg, and Rh are each hydrogen; or
(viii) Rc and Rd together form ═O; and Ra, Rb, Re, Rf, Rg, and Rh are each hydrogen; or
(ix) Rc and Re form a C1-C4 alkylene group between the atoms to which they are attached; and Ra, Rb, Rd, Rf, Rg, and Rh are each hydrogen; or
(x) Rc and Rg form a C1-C3 alkylene group between the atoms to which they are attached; and Ra, Rb, Rd, Re, Rf, and Rh are each hydrogen; or
(xi) Re and Rf together with the atom to which they are attached, form a 3-6 membered cycloalkyl or heterocycloalkyl; and Ra, Rb, Rc, Rd, Rg, and Rh are each hydrogen; or
(xiii) Re and Rg form a C1-C3 alkylene group between the atoms to which they are attached; and Ra, Rb, Rc, Rd, Rf, and Rh are each independently hydrogen; or
(xv) Rg and Rh together form ═O; and Ra, Rb, Rc, Rd, Re, and Rf are each hydrogen.
In some embodiments, the disclosure relates to a compound of formula (I), (I-A), (I-B), (I-C), (I-D), (I-E), or (I-M), or a pharmaceutically acceptable salt thereof, wherein Ra, Rb, Rc, Rd, Re, Rf, Rg, and Rh are defined as follows:
(ii) Ra and Re form a C1-C2 alkylene group between the atoms to which they are attached; and Rb, Rc, Rd, Rf, Rg, and Rh are each hydrogen; or
(iv) Rb and Rc form a C1-C3 alkylene group between the atoms to which they are attached, and Ra, Rd, Re, Rf, Rg and Rh are each hydrogen; or
(vii) Rc and Rd together with the atom to which they are attached, form a 3-membered cycloalkyl or a 4-membered heterocycloalkyl; and Ra, Rb, Re, Rf, Rg, and Rh are each hydrogen; or
(viii) Rc and Rd together form ═O; and Ra, Rb, Re, Rf, Rg, and Rh are each hydrogen; or
(ix) Rc and Re form a C1 alkylene group between the atoms to which they are attached; and Ra, Rb, Rd, Rf, Rg, and Rh are each hydrogen; or
(x) Rc and Rg form a C1-C2 alkylene group between the atoms to which they are attached; and Ra, Rb, Rd, Re, Rf, and Rh are each hydrogen; or
(xi) Re and Rf together with the atom to which they are attached, form a 4-membered heterocycloalkyl; and Ra, Rb, Rc, Rd, Rg, and Rh are each hydrogen; or
(xiii) Re and Rg form a C2 alkylene group between the atoms to which they are attached; and Ra, Rb, Rc, Rd, Rf, and Rh are each independently hydrogen; or
(xv) Rg and Rh together form ═O; and Ra, Rb, Rc, Rd, Re, and Rf are each hydrogen.
In some embodiments, the disclosure relates to a compound of formula (I), (I-A), (I-B), (I-C), (I-D), (I-E), or (I-M), or a pharmaceutically acceptable salt thereof, wherein Ra, Rb, Rc, Rd, Re, Rf, Rg, and Rh are defined as follows:
(ii) Ra and Re form a C1-C2 alkylene group between the atoms to which they are attached; and Rb, Rc, Rd, Rf, and Rg are each hydrogen; or
(iv) Rb and Rc form a C1-C2 alkylene group between the atoms to which they are attached; and Ra, Rc, Rd, Rf, and Rg are each hydrogen; or
(vii) Rc and Rd together with the atom to which they are attached, form a 3 membered cycloalkyl; and Ra, Rb, Re, Rf, and Rg are each hydrogen; or
(x) Rc and Rg form a C1-C2 alkylene group between the atoms to which they are attached; and Ra, Rb, Rd, Re, and Rg are each hydrogen; or
(xi) Re and Rf together with the atom to which they are attached, form a 4 membered heterocycloalkyl; and Ra, Rb, Rc, Rd, and Rg are each hydrogen; or
(xiii) Re and Rg form a C2 alkylene group between the atoms to which they are attached; and Ra, Rb, Rc, Rd, and Rf are each independently hydrogen.
In some embodiments, the disclosure relates to a compound of formula (I), (I-A), (I-B), (I-C), (I-D), (I-E), or (I-M), or a pharmaceutically acceptable salt thereof, wherein
is selected from:
In some embodiments,
In some embodiments.
In some embodiments,
In some embodiments,
In some embodiments,
In some embodiments,
In some embodiments,
In some embodiments,
In some embodiments,
In some embodiments,
In some embodiments,
In some embodiments, the disclosure relates to a compound of formula (I-A), (I-A-1), (I-A-2), (I-A-3), (I-A-4), (I-B), (I-B-1), (I-B-2), (I-B-3), (I-B-4), (I-F-1), (I-F-2), (I-G-1), (I-G-2), (I-H-1), (I-H-2), (I-J-1), (I-J-2), (I-K-1), (I-K-2), (I-L-1), (I-L-2), (I-M), (I-M-1), (I-M-2), (I-M-3), or (I-M-4), or a pharmaceutically acceptable salt thereof, wherein X1 is C or N. In some embodiments, X1 is C. In some embodiments, X1 is N.
In some embodiments, the disclosure relates to a compound of formula (I-A), (I-A-1), (I-A-2), (I-A-3), (I-A-4), (I-B), (I-B-1), (I-B-2), (I-B-3), (I-B-4), (I-F-1), (I-F-2), (I-G-1), (I-G-2), (I-H-1), (I-H-2), (I-J-1), (I-J-2), (I-K-1), (I-K-2), (I-L-1), (I-L-2), (I-M), (I-M-1), (I-M-2), (I-M-3), or (I-M-4), or a pharmaceutically acceptable salt thereof, wherein X2 is CH, CR1, O, S, N, NH, or NR1, as valency permits. In some embodiments, X2 is CH. In some embodiments, X2 is CR1. In some embodiments, X2 is O. In some embodiments, X2 is S. In some embodiments, X2 is N. In some embodiments, X2 is NH. In some embodiments, X2 is NR1.
In some embodiments, the disclosure relates to a compound of formula (I-A), (I-A-1), (I-A-2), (I-A-3), (I-A-4), (I-B), (I-B-1), (I-B-2), (I-B-3), (I-B-4), (I-F-1), (I-F-2), (I-G-1), (I-G-2), (I-H-1), (I-H-2), (I-J-1), (I-J-2), (I-K-1), (I-K-2), (I-L-1), (I-L-2), (I-M), (I-M-1), (I-M-2), (I-M-3), or (I-M-4), or a pharmaceutically acceptable salt thereof, wherein X3 is CH, CR1, O, S, N, NH, or NR1, as valency permits. In some embodiments, X3 is CH. In some embodiments, X3 is CR1. In some embodiments, X3 is O. In some embodiments, X3 is S. In some embodiments, X3 is N. In some embodiments, X3 is NH. In some embodiments, X3 is NR1.
In some embodiments, the disclosure relates to a compound of formula (I-A), (I-A-1), (I-A-2), (I-A-3), (I-A-4), (I-B), (I-B-1), (I-B-2), (I-B-3), (I-B-4), (I-F-1), (I-F-2), (I-G-1), (I-G-2), (I-H-1), (I-H-2), (I-J-1), (I-J-2), (I-K-1), (I-K-2), (I-L-1), (I-L-2), (I-M), (I-M-1), (I-M-2), (I-M-3), or (I-M-4), or a pharmaceutically acceptable salt thereof, wherein X4 is C or N. In some embodiments, X4 is C. In some embodiments, X4 is N.
In some embodiments, the disclosure relates to a compound of formula (I-A), (I-A-1), (I-A-2), (I-A-3), (I-A-4), (I-F-1), (I-F-2), (I-G-1), (I-G-2), (I-H-1), (I-H-2), (I-J-1), (I-J-2), (I-K-1), (I-K-2), (I-L-1), (I-L-2), (I-M), (I-M-1), (I-M-2), (I-M-3), or (I-M-4), or a pharmaceutically acceptable salt thereof, wherein X5 is a bond, CH, CR1, O, S, N, NH, or NR1, as valency permits. In some embodiments, X5 is a bond. In some embodiments, X5 is CH. In some embodiments, X5 is CR1. In some embodiments, X5 is O. In some embodiments, X5 is S. In some embodiments, X5 is N. In some embodiments, X5 is NH. In some embodiments, X5 is NR1.
In some embodiments, the disclosure relates to a compound of formula (I-A), (I-A-1), (I-A-2), (I-A-3), (I-A-4), (I-B), (I-B-1), (I-B-2), (I-B-3), (I-B-4), (I-F-1), (I-F-2), (I-G-1), (I-G-2), (I-H-1), (I-H-2), (I-J-1), (I-J-2), (I-K-1), (I-K-2), (I-L-1), (I-L-2), (I-M), (I-M-1), (I-M-2), (I-M-3), or (I-M-4), or a pharmaceutically acceptable salt thereof, wherein X6 is CH, CR1, O, S, N, NH, or NR1, as valency permits. In some embodiments, X6 is CH. In some embodiments, X6 is CR1. In some embodiments, X6 is O. In some embodiments, X6 is S. In some embodiments, X6 is N. In some embodiments, X6 is NH. In some embodiments, X6 is NR1.
In some embodiments, the disclosure relates to a compound of formula (I-A), (I-A-1), (I-A-2), (I-A-3), (I-A-4), (I-F-1), (I-F-2), (I-G-1), (I-G-2), (I-H-1), (I-H-2), (I-J-1), (I-J-2), (I-K-1), (I-K-2), (I-L-1), (I-L-2), (I-M), (I-M-1), (I-M-2), (I-M-3), or (I-M-4), or a pharmaceutically acceptable salt thereof, wherein X1 is C; X2 is N; X3 is NH; X4 is C; X5 is a bond; and X6 is CH.
In some embodiments, the disclosure relates to a compound of formula (I-A), (I-A-1), (I-A-2), (I-A-3), (I-A-4), (I-F-1), (I-F-2), (I-G-1), (I-G-2), (I-H-1), (I-H-2), (I-J-1), (I-J-2), (I-K-1), (I-K-2), (I-L-1), (I-L-2), (I-M), (I-M-1), (I-M-2), (I-M-3), or (I-M-4), or a pharmaceutically acceptable salt thereof, wherein X1 is C; X2 is N; X3 is CH; X4 is C; X5 is a bond; and X6 is S.
In some embodiments, the disclosure relates to a compound of formula (I-A), (I-A-1), (I-A-2), (I-A-3), (I-A-4), (I-F-1), (I-F-2), (I-G-1), (I-G-2), (I-H-1), (I-H-2), (I-J-1), (I-J-2), (I-K-1), (I-K-2), (I-L-1), (I-L-2), (I-M), (I-M-1), (I-M-2), (I-M-3), or (I-M-4), or a pharmaceutically acceptable salt thereof, wherein X1 is C; X2 is CH; X3 is CH; X4 is C; X5 is CH; and X6 is C.
In some embodiments, the disclosure relates to a compound of formula (I-A), (I-A-1), (I-A-2), (I-A-3), (I-A-4), (I-F-1), (I-F-2), (I-G-1), (I-G-2), (I-H-1), (I-H-2), (I-J-1), (I-J-2), (I-K-1), (I-K-2), (I-L-1), or (I-L-2), or a pharmaceutically acceptable salt thereof, wherein Y1 is C or N. In some embodiments, Y1 is C. In some embodiments, Y1 is N.
In some embodiments, the disclosure relates to a compound of formula (I-A), (I-A-1), (I-A-2), (I-A-3), (I-A-4), (I-F-1), (I-F-2), (I-G-1), (I-G-2), (I-H-1), (I-H-2), (I-J-1), (I-J-2), (I-K-1), (I-K-2), (I-L-1), or (I-L-2), or a pharmaceutically acceptable salt thereof, wherein Y2 is C or N. In some embodiments, Y2 is C. In some embodiments, Y2 is N.
In some embodiments, the disclosure relates to a compound of formula (I-A), (I-A-1), (I-A-2), (I-A-3), (I-A-4), (I-B), (I-B-1), (I-B-2), (I-B-3), (I-B-4), (I-F-1), (I-F-2), (I-G-1), (I-G-2), (I-H-1), (I-H-2), (I-J-1), (I-J-2), (I-K-1), (I-K-2), (I-L-1), or (I-L-2), or a pharmaceutically acceptable salt thereof, wherein Y3 is CH, CR2, O, S, N, NH, or NR2, as valency permits. In some embodiments, Y3 is CH. In some embodiments, Y3 is CR2. In some embodiments, Y3 is O. In some embodiments, Y3 is S. In some embodiments, Y3 is N. In some embodiments, Y3 is NH. In some embodiments, Y3 is NR2.
In some embodiments, the disclosure relates to a compound of formula (I-A), (I-A-1), (I-A-2), (I-A-3), (I-A-4), (I-B), (I-B-1), (I-B-2), (I-B-3), (I-B-4), (I-F-1), (I-F-2), (I-G-1), (I-G-2), (I-H-1), (I-H-2), (I-J-1), (I-J-2), (I-K-1), (I-K-2), (I-L-1), or (I-L-2), or a pharmaceutically acceptable salt thereof, wherein Y4 is a bond, CH, CR2, O, S, N, NH, or NR2, as valency permits. In some embodiments, Y4 is a bond. In some embodiments, Y4 is CH. In some embodiments, Y4 is CR2. In some embodiments, Y4 is O. In some embodiments, Y4 is S. In some embodiments, Y4 is N. In some embodiments, Y4 is NH. In some embodiments, Y4 is NR2.
In some embodiments, the disclosure relates to a compound of formula (I-A), (I-A-1), (I-A-2), (I-A-3), (I-A-4), (I-B), (I-B-1), (I-B-2), (I-B-3), (I-B-4), (I-F-1), (I-F-2), (I-G-1), (I-G-2), (I-H-1), (I-H-2), (I-J-1), (I-J-2), (I-K-1), (I-K-2), (I-L-1), or (I-L-2), or a pharmaceutically acceptable salt thereof, wherein Y5 is CH, CR2, O, S, N, NH, or NR2, as valency permits. In some embodiments, Y5 is CH. In some embodiments, Y5 is CR2. In some embodiments, Y5 is O. In some embodiments, Y5 is S. In some embodiments, Y5 is N. In some embodiments, Y5 is NH. In some embodiments, Y5 is NR2.
In some embodiments, the disclosure relates to a compound of formula (I-A), (I-A-1), (I-A-2), (I-A-3), (I-A-4), (I-B), (I-B-1), (I-B-2), (I-B-3), (I-B-4), (I-F-1), (I-F-2), (I-G-1), (I-G-2), (I-H-1), (I-H-2), (I-J-1), (I-J-2), (I-K-1), (I-K-2), (I-L-1), or (I-L-2), or a pharmaceutically acceptable salt thereof, wherein Y6 is CH, CR2, O, S, N, NH, or NR2, as valency permits. In some embodiments, Y6 is CH. In some embodiments, Y6 is CR2. In some embodiments, Y6 is O. In some embodiments, Y6 is S. In some embodiments, Y6 is N. In some embodiments, Y6 is NH. In some embodiments, Y6 is NR2.
In some embodiments, the disclosure relates to a compound of formula (I-A), (I-A-1), (I-A-2), (I-A-3), (I-A-4), (I-F-1), (I-F-2), (I-G-1), (I-G-2), (I-H-1), (I-H-2), (I-J-1), (I-J-2), (I-K-1), (I-K-2), (I-L-1), or (I-L-2), or a pharmaceutically acceptable salt thereof, wherein Y1 is C; Y2 is C; Y3 is CH; Y4 is CH; Y5 is CH; and Y6 is CH.
In some embodiments, the disclosure relates to a compound of formula (I-A), (I-A-1), (I-A-2), (I-A-3), (I-A-4), (I-F-1), (I-F-2), (I-G-1), (I-G-2), (I-H-1), (I-H-2), (I-J-1), (I-J-2), (I-K-1), (I-K-2), (I-L-1), or (I-L-2), or a pharmaceutically acceptable salt thereof, wherein Y1 is C; Y2 is C; Y3 is CR2; Y4 is CH; Y5 is CH; and Y6 is CH.
In some embodiments, the disclosure relates to a compound of formula (I-A), (I-A-1), (I-A-2), (I-A-3), (I-A-4), (I-F-1), (I-F-2), (I-G-1), (I-G-2), (I-H-1), (I-H-2), (I-J-1), (I-J-2), (I-K-1), (I-K-2), (I-L-1), or (I-L-2), or a pharmaceutically acceptable salt thereof, wherein Y1 is C; Y2 is C; Y3 is CH; Y4 is CR2; Y5 is CH; and Y6 is CH.
In some embodiments, the disclosure relates to a compound of formula (I-A), (I-A-1), (I-A-2), (I-A-3), (I-A-4), (I-F-1), (I-F-2), (I-G-1), (I-G-2), (I-H-1), (I-H-2), (I-J-1), (I-J-2), (I-K-1), (I-K-2), (I-L-1), or (I-L-2), or a pharmaceutically acceptable salt thereof, wherein Y1 is C; Y2 is C; Y3 is CH; Y4 is CH; Y5 is CR2; and Y6 is CH.
In some embodiments, the disclosure relates to a compound of formula (I-A), (I-A-1), (I-A-2), (I-A-3), (I-A-4), (I-F-1), (I-F-2), (I-G-1), (I-G-2), (I-H-1), (I-H-2), (I-J-1), (I-J-2), (I-K-1), (I-K-2), (I-L-1), or (I-L-2), or a pharmaceutically acceptable salt thereof, wherein Y1 is C; Y2 is C; Y3 is N; Y4 is CH; Y5 is CH; and Y6 is CR2. In some embodiments, the disclosure relates to a compound of formula (I-A), or a pharmaceutically acceptable salt thereof, wherein Y1 is C; Y2 is C; Y3 is N; Y4 is CH; Y5 is CH; and Y6 is CH.
In some embodiments, the disclosure relates to a compound of formula (I-A), (I-A-1), (I-A-2), (I-A-3), (I-A-4), (I-F-1), (I-F-2), (I-G-1), (I-G-2), (I-H-1), (I-H-2), (I-J-1), (I-J-2), (I-K-1), (I-K-2), (I-L-1), or (I-L-2), or a pharmaceutically acceptable salt thereof, wherein Y1 is C; Y2 is C; Y3 is CH; Y4 is N; Y5 is CH; and Y6 is CH.
In some embodiments, the disclosure relates to a compound of formula (I-A), (I-A-1), (I-A-2), (I-A-3), (I-A-4), (I-F-1), (I-F-2), (I-G-1), (I-G-2), (I-H-1), (I-H-2), (I-J-1), (I-J-2), (I-K-1), (I-K-2), (I-L-1), or (I-L-2), or a pharmaceutically acceptable salt thereof, wherein Y1 is C; Y2 is C; Y3 is CH; Y4 is CH; Y5 is N; and Y6 is CH.
In some embodiments, the disclosure relates to a compound of formula (I-A), (I-A-1), (I-A-2), (I-A-3), (I-A-4), (I-F-1), (I-F-2), (I-G-1), (I-G-2), (I-H-1), (I-H-2), (I-J-1), (I-J-2), (I-K-1), (I-K-2), (I-L-1), or (I-L-2), or a pharmaceutically acceptable salt thereof, wherein Y1 is C; Y2 is C; Y3 is CH; Y4 is CH; Y5 is CH; and Y6 is N.
In some embodiments, the disclosure relates to a compound of formula (I-A-1), (I-A-2), (I-A-3), (I-A-4), (I-B-1), (I-B-2), (I-B-3), (I-B-4), (I-C-1), (I-C-2), (I-C-3), (I-C-4), (I-M-1), (I-M-2), (I-M-3), or (I-M-4), or a pharmaceutically acceptable salt thereof, wherein Rj, Rk, Rm, Rn, Ro, Rp, Rq, and Rr, when present, are each independently hydrogen, halogen, C1-C3 alkyl, or C1-C3 haloalkyl. In some embodiments, Rj, Rk, Rm, Rn, Ro, Rp, Rq, and Rr, when present, are each hydrogen.
In some embodiments, the disclosure relates to a compound of formula (I-B), (I-B-1), (I-B-2), (I-B-3), or (I-B-4), or a pharmaceutically acceptable salt thereof, wherein X1 is C; X2 is N; X3 is NH; X4 is C; and X6 is CH.
In some embodiments, the disclosure relates to a compound of formula (I-B), (I-B-1), (I-B-2), (I-B-3), or (I-B-4), or a pharmaceutically acceptable salt thereof, wherein X1 is C; X2 is N; X3 is CH; X4 is C; and X6 is S.
In some embodiments, the disclosure relates to a compound of formula (I-B), (I-B-1), (I-B-2), (I-B-3), or (I-B-4), or a pharmaceutically acceptable salt thereof, wherein Y3 is CH; Y4 is CH; Y5 is CH; and Y6 is CH.
In some embodiments, the disclosure relates to a compound of formula (I-B), (I-B-1), (I-B-2), (I-B-3), or (I-B-4), or a pharmaceutically acceptable salt thereof, wherein Y3 is CR2; Y4 is CH; Y5 is CH; and Y6 is CH.
In some embodiments, the disclosure relates to a compound of formula (I-B), (I-B-1), (I-B-2), (I-B-3), or (I-B-4), or a pharmaceutically acceptable salt thereof, wherein Y3 is CH; Y4 is CR2; Y5 is CH; and Y6 is CH.
In some embodiments, the disclosure relates to a compound of formula (I-B), (I-B-1), (I-B-2), (I-B-3), or (I-B-4), or a pharmaceutically acceptable salt thereof, wherein Y3 is CH; Y4 is CH; Y5 is CR2; and Y6 is CH
In some embodiments, the disclosure relates to a compound of formula (I-B), (I-B-1), (I-B-2), (I-B-3), or (I-B-4), or a pharmaceutically acceptable salt thereof, wherein Y3 is CH; Y4 is CH; Y5 is CH; and Y6 is CR2.
In some embodiments, the disclosure relates to a compound of formula (I-B), (I-B-1), (I-B-2), (I-B-3), or (I-B-4), or a pharmaceutically acceptable salt thereof, wherein Y3 is N; Y4 is CH; Y5 is CH; and Y6 is CH.
In some embodiments, the disclosure relates to a compound of formula (I-B), (I-B-1), (I-B-2), (I-B-3), or (I-B-4), or a pharmaceutically acceptable salt thereof, wherein Y3 is CH; Y4 is N; Y5 is CH, and Y6 is CH.
In some embodiments, the disclosure relates to a compound of formula (I-B), (I-B-1), (I-B-2), (I-B-3), or (I-B-4), or a pharmaceutically acceptable salt thereof, wherein Y3 is CH; Y4 is CH; Y5 is N, and Y6 is CH.
In some embodiments, the disclosure relates to a compound of formula (I-B), (I-B-1), (I-B-2), (I-B-3), or (I-B-4), or a pharmaceutically acceptable salt thereof, wherein Y3 is CH; Y4 is CH; Y5 is CH; and Y6 is N.
In some embodiments, the disclosure relates to a compound provided herein, or a pharmaceutically acceptable salt thereof, that is a USP30 Inhibitor Compound having an IC50 value of ≤1 μM and >0.001 μM as measured in a Ubiquitin-Rhodamine 110 Assay as described in Example 1.
In another aspect, the disclosure relates to a compound selected from Table 1, or a pharmaceutically acceptable salt thereof. Each pair of compounds listed in Table 1 (i.e., compounds 1-a and 1-b, compounds 2-a and 2-b, etc.) was obtained as a racemic mixture, and were then separated by chiral HPLC according to the procedure described in Example 2, Step 7, or a similar method, to obtain the individual compounds in substantially enantiomerically pure form. For each pair of compounds, the first compound (i.e., compounds 1-a, 2-a, etc.) was the first eluting isomer, and the second compound (i.e., compounds 1-b, 2-b, etc.) was the second eluting isomer. The stereochemical descriptors reflect the relative stereochemistry of each compound. The absolute stereochemistry of each compound was arbitrarily assigned. In some embodiments, the compound selected from Table 1, or a pharmaceutically acceptable salt thereof, is present in a racemic mixture. In some embodiments, the compound selected from Table 1, or a pharmaceutically acceptable salt thereof, is present in substantially enantiomerically pure form.
In another aspect, the disclosure relates to a compound selected from Table 2, or a pharmaceutically acceptable salt thereof. In some embodiments, the compound, or a pharmaceutically acceptable salt thereof, is present in a racemic mixture with its enantiomer. In some embodiments, the compound, or a pharmaceutically acceptable salt thereof, is present in substantially enantiomerically pure form.
In another aspect, the disclosure relates to the enantiomer of a compound selected from Table 2, or a pharmaceutically acceptable salt thereof. In some embodiments, the enantiomer, or a pharmaceutically acceptable salt thereof, is present in a racemic mixture. In some embodiments, the enantiomer, or a pharmaceutically acceptable salt thereof, is present in substantially enantiomerically pure form.
In some embodiments, a compound described herein is provided in non-salt form. In some embodiments, a compound described herein is provided as a pharmaceutically acceptable salt.
In another aspect, the disclosure relates to a compound, or a pharmaceutically acceptable salt thereof, prepared by a method comprising: preparing a compound of the present disclosure as a mixture of stereoisomers; separating the stereoisomers by chiral HPLC according to the procedure described in Example 2, Step 7; isolating one or more stereoisomers that are USP30 Inhibitor Compounds having an IC50 value of <1 μM as measured in a Ubiquitin-Rhodamine 110 Assay as described in Example 1; and optionally treating the isolated stereoisomer with an acid or base to afford a pharmaceutically acceptable salt thereof.
In some embodiments, the compound is the 1st eluting isomer. In some embodiments, the compound is the 2nd eluting isomer. In some embodiments, the compound is the 3rd eluting isomer. In some embodiments, the compound is the 4th eluting isomer. In some embodiments, the compound is the 5th, 6th, 7th, or 8th eluting isomer.
In some embodiments, a compound of the present disclosure, or a pharmaceutically acceptable salt thereof, is a USP30 Inhibitor Compound having an IC50 value of ≤1 μM as measured in a Ubiquitin-Rhodamine 110 Assay as described in Example 1. In some embodiments, the IC50 value is ≤0.1 μM.
Pharmaceutical Compositions and Routes of Administration
The disclosure also relates to a pharmaceutical composition comprising one or more compounds provided herein, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier. In some embodiments, the pharmaceutical composition comprises a therapeutically effective amount of the one or more compounds, or a pharmaceutically acceptable salt thereof. In some embodiments, the pharmaceutical composition is for use in a method of treating a neurodegenerative disorder, such as Parkinson's Disease.
The compounds and pharmaceutically acceptable salts disclosed herein may be administered via any mode of administration for therapeutic agents, consistent with conventional pharmaceutical practices. In some embodiments, the pharmaceutical compositions reported herein can be provided in a unit dosage form. In some embodiments, the pharmaceutical compositions reported herein can be provided in an oral dosage form. In some embodiments, the pharmaceutical compositions described herein can be provided in a solid oral dosage form, such as a tablet, capsule, powder, or cachet.
The pharmaceutical compositions described herein can be prepared according to conventional mixing, granulating or coating methods. For example, oral dosage forms (e.g., tablets) may be prepared by dry blending or dry granulation. The pharmaceutical compositions described herein can contain from about 0.1% to about 99%, from about 5% to about 90%, or from about 1% to about 20% of the compound or pharmaceutically acceptable salt by weight or volume. The pharmaceutically acceptable carriers employed in the pharmaceutical compositions described herein may include one or more pharmaceutical excipients, such as fillers, disintegrants, lubricants, glidants, anti-adherents, anti-statics, surfactants, or stabilizing additives. Suitable solid carriers are known in the art, e.g., magnesium carbonate, magnesium stearate, talc, sugar or lactose. With some drugs, the presence of such additives promotes the stability and dispersibility of the agent in solution. Suitable, but non-limiting, examples of stabilizing additives include gum acacia, gelatin, methyl cellulose, polyethylene glycol, carboxylic acids and salts thereof, and polylysine. In some embodiments, the stabilizing additives are gum acacia, gelatin and methyl cellulose. Examples of pharmaceutically acceptable carriers and methods of manufacture for various compositions may be found in A. Gennaro (ed.), Remington's Pharmaceutical Sciences, 18th Edition, (1990), Mack Publishing Co., Easton, Pa.
The pharmaceutical compositions described herein may contain the compound or pharmaceutically acceptable salt in substantially pure form, such as at least 60% pure, more suitably at least 75% pure, preferably at least 85% pure and most preferably at least 98% pure (w/w).
The compounds and pharmaceutically acceptable salts described herein are preferably administered in a therapeutically effective amount (e.g., an amount having a suitable favorable therapeutic index). The amount and frequency of administration will be regulated according to the judgment of the attending clinician considering such factors as the age, gender, condition and size of the patient, as well as severity of the medical condition being treated; the route of administration; the renal or hepatic function of the patient; and the particular compound or pharmaceutically acceptable salt employed. A physician or veterinarian of ordinary skill in the art can readily determine and prescribe the effective amount of the drug required to prevent, counter or arrest the progress of the condition. For convenience, the total daily dosage may be divided and administered in portions during the day as required.
Uses of Compounds Disclosed Herein
The present disclosure also provides uses of compounds of formula (I). Compounds of formula (I) are useful in medicine. For examples, compounds and compositions described herein are inhibitors of USP30. Without wishing to be bound by any particular theory, such inhibition of USP30 can provide treatment of the symptoms and/or underlying causes of diseases or conditions associated with USP30 activity. In some embodiments, inhibitors of USP30 can be used to treat neurodegenerative and neurologic diseases or conditions, such as Parkinson's disease.
Provided herein are methods of treating a disease or disorder associated with a ubiquitin-specific protease (e.g., USP30), comprising administering to a patient in need thereof a therapeutically effective amount of a compound or composition provided herein. In some embodiments, the disease or disorder associated with a ubiquitin-specific protease (e.g., USP30) is a neurodegenerative disease or disorder (e.g., Parkinson's disease).
The present disclosure also provides methods of inhibiting a ubiquitin-specific protease (e.g., USP30) in a patient in need thereof, comprising administering to the patient a therapeutically effective amount of a compound or composition provided herein.
The present disclosure also provides methods of treating a neurodegenerative disease or disorder (e.g., Parkinson's disease) in a patient in need thereof, comprising administering to the patient a therapeutically effective amount of a compound or composition provided herein.
The present disclosure also provides compounds for use in method of inhibiting a ubiquitin-specific protease (e.g., USP30) in a patient in need thereof. In some embodiments, the present disclosure provides compounds for use in a method of treating a neurodegenerative disease or disorder (e.g., Parkinson's disease) in a patient in need thereof.
Synthesis of Compounds Disclosed Herein
The compounds and pharmaceutically acceptable salts disclosed herein may be prepared by methods known in the art of organic synthesis as set forth in part by the following synthetic schemes. In the schemes described below, it is well understood that protecting groups for sensitive or reactive groups are employed where necessary in accordance with general principles of chemistry. Protecting groups are manipulated according to standard methods of organic synthesis (T. W. Greene and P. G. M. Wuts, “Protective Groups in Organic Synthesis”, Third edition, Wiley, New York 1999). These groups are removed at a convenient stage of the compound synthesis using methods that are readily apparent to those skilled in the art.
In general, the compounds of formula (I) can be synthesized by the methods outlined in Scheme 1, by the specific procedures discussed in Examples 2-4, and/or by methods otherwise known to one skilled in the art. The starting materials for the synthesis described in Scheme 1 are commercially available or can be prepared by methods known to one skilled in the art.
The following numbered embodiments, while non-limiting, are exemplary of certain aspects of the disclosure:
or a pharmaceutically acceptable salt thereof, wherein:
Ar1 is phenylene or 5-6 membered heteroarylene, wherein said phenylene or heteroarylene is substituted with m R1 groups;
Ar2 is phenylene or 5-6 membered heteroarylene, wherein said phenylene or heteroarylene is substituted with n R2 groups;
L is —O—, —S—, —NR3—, —C(R4)2—, —S(O)2—, or —S(O)—;
M is 3-6 membered cycloalkyl, phenyl, or 5-6 membered heteroaryl, wherein said cycloalkyl, phenyl, or heteroaryl is substituted with p R5 groups;
each occurrence of R1, R2, and R5 is independently halo, cyano, NO2, oxo, hydroxyl, —R6, —OR6, C1-C6 alkyl, C1-C6 haloalkyl, C1-C6 hydroxyalkyl, —C1-C6 alkylene-R6, C1-C6 alkoxy, C1-C6 haloalkoxy, —C0-C3 alkylene-NR6R7, —C0-C3 alkylene-NR7R8, —C0-C3 alkylene-C(O)NR6R7, —C0-C3 alkylene-C(O)NR7R8, —C0-C3 alkylene-NR7C(O)R6, —C0-C3 alkylene-NR7C(O)R8, —C0-C3 alkylene-NR7S(O)2R6, —C0-C3 alkylene-C(O)R6, —C0-C3 alkylene-C(O)R7, —C0-C3 alkylene-SR6, —C0-C3 alkylene-S(O)R6, —C0-C3 alkylene-S(O)2R6, —C0-C3 alkylene-S(O)2R7, —C0-C3 alkylene-S(O)2NR6R7, —C0-C3 alkylene-S(O)2NR7R8, —C0-C3 alkylene-NR7C(O)NR8R9, —C0-C3 alkylene- NR7S(O)2NR8R9, —C0-C3 alkylene-C(O)OR7, —C0-C3 alkylene-C(O)OR6, —C0-C3 alkylene-OC(O)R7, —C0-C3 alkylene-OC(O)R6, —C0-C3 alkylene-NR7C(O)OR8, or —C0-C3 alkylene-NR7S(O)2R8;
R3 is H, C1-C6 alkyl, or C1-C6 haloalkyl;
each R4 is independently H, C1-C6 alkyl, C1-C6 haloalkyl, or two R4 groups together with the carbon atom to which they are attached form a 3-6 membered cycloalkyl or heterocycloalkyl;
each R6 is independently 5-10 membered heteroaryl, 4-10 membered heterocycloalkyl, 6-10 membered aryl, or 3-8 membered cycloalkyl, wherein said heteroaryl, heterocycloalkyl, aryl, or cycloalkyl is optionally substituted with 1-5 substituents independently selected from the group consisting of halo, oxo, C1-C6 alkyl, C1-C6 haloalkyl, C1-C6 hydroxyalkyl, C1-C6 alkoxy, C1-C6 haloalkoxy, C2-C6 alkenyl, C2-C6 alkynyl, 5-10 membered heteroaryl, 4-10 membered heterocycloalkyl, 6-10 membered aryl, 3-8 membered cycloalkyl, —NR10C(O)NR11R12, —NR10R11, —C(O)R10, —NR10C(O)R11, —NR10C(O)OR11, —S(O)2R10, —C(O)NR10R11, —C(O)OR10, —S(O)2NR10R11, —NR10S(O)2R11, —OR10, —OC(O)R10, —OS(O)2R10, —OC(O)NR10R11, —OC(O)OR10, —OS(O)2NR10R11, —C(O)R10, —C(O)NR10C(O)NR11R12, —C(O)NR10R11, —C(O)C(O)R10, —C(O)NR10C(O)R11, —C(O)NR10C(O)OR11, —C(O)S(O)2R10, —C(O)C(O)NR10R11, —C(O)C(O)OR10, —C(O)S(O)2NR10R11, —C(O)NR10S(O)2R11, —C1-C6 alkylene-R10, —C1-C6 alkylene-NR10C(O)NR11R12, —C1-C6 alkylene-NR10R11, —C1-C6 alkylene-C(O)R10, —C1-C6 alkylene-NR10C(O)R11, —C1-C6 alkylene-NR10C(O)OR11, —C1-C6 alkylene-S(O)2R10, —C1-C6 alkylene-C(O)NR10R11, —C1-C6 alkylene-C(O)OR10, —C1-C6 alkylene-S(O)2NR10R11, —C1-C6 alkylene-NR10S(O)2R11, —C1-C6 alkenylene-R10, —C1-C6 alkenylene-NR10C(O)NR11R12, —C1-C6 alkenylene-NR10R11, —C1-C6 alkenylene-C(O)R10, —C1-C6 alkenylene-NR10C(O)R11, —C1-C6 alkenylene-NR10C(O)OR11, —C1-C6 alkenylene-S(O)2R10, —C1-C6 alkenylene-C(O)NR10R11, —C1-C6 alkenylene-C(O)OR10, —C1-C6 alkenylene-S(O)2NR10R11, and —C1-C6 alkenylene-NR10S(O)2R11;
each R7, R8, and R9 is independently hydrogen or C1-C6 alkyl;
each R10, R11, and R12 is independently hydrogen, C1-C6 alkyl, 5-10 membered heteroaryl, 4-10 membered heterocycloalkyl, 6-10 membered aryl, or 3-8 membered cycloalkyl;
m is 0-4;
n is 0-4;
p is 0-4;
Ra, Rb, Rc, Rd, Re, Rf, Rg, and Rh are defined as follows:
or a pharmaceutically acceptable salt thereof, wherein:
X1 is C or N;
X2 is CH, CR1, O, S, N, NH, or NR1;
X3 is CH, CR1, O, S, N, NH, or NR1;
X4 is C or N;
X5 is a bond, CH, CR1, O, S, N, NH, or NR1;
X6 is CH, CR1, O, S, N, NH, or NR1;
Y1 is C or N;
Y2 is C or N;
Y3 is CH, CR2, O, S, N, NH, or NR2;
Y4 is a bond, CH, CR2, O, S, N, NH, or NR2;
Y5 is CH, CR2, O, S, N, NH, or NW;
Y6 is CH, CR2, O, S, N, NH, or NR2;
Ra, Rb, Rc, Rd, Re, Rf, Rg, and Rh are defined as follows:
or a pharmaceutically acceptable salt thereof, wherein:
X1 is C or N;
X2 is CH, CR1, O, S, N, NH, or NR1;
X3 is CH, CR1, O, S, N, NH, or NR1;
X4 is C or N;
X6 is CH, CR1, O, S, N, NH, or NR1;
Y3 is CH, CR2, or N,
Y4 is CH, CR2, or N;
Y5 is CH, CR2, or N;
Y6 is CH, CR2, or N;
Ra, Rb, Rc, Rd, Re, Rf, Rg, and Rh are defined as follows:
or a pharmaceutically acceptable salt thereof, wherein:
Ra, Rb, Rc, Rd, Re, Rf, Rg, and Rh are defined as follows:
or a pharmaceutically acceptable salt thereof, that is a USP30 Inhibitor Compound having an IC50 value of ≤1 μM and >0.001 μM as measured in a Ubiquitin-Rhodamine 110 Assay as described in Example 1, wherein:
each occurrence of R2 and R5 is independently halo, cyano, hydroxyl, C1-C6 alkyl, C1-C6 alkoxyl, C1-C6 haloalkyl, and C1-C6 hydroxyalkyl;
n is 0-4;
p is 0-4;
Rh is hydrogen;
Ra, Rb, Rc, Rd, Re, Rf, and Rg are defined as follows:
or a pharmaceutically acceptable salt thereof, wherein:
each occurrence of R2 and R5 is independently halo, cyano, hydroxyl, C1-C6 alkyl, C1-C6 alkoxyl, C1-C6 haloalkyl, or C1-C6 hydroxyalkyl;
n is 0-4;
p is 0-4.
General Methods
All solvents used were commercially available and were used without further purification. Reactions were typically run using anhydrous solvents under an inert atmosphere of nitrogen.
Proton NMR spectra were recorded using a Broker Plus 400 NMR Spectrometer. The deuterated solvent (DMSO-d6) typically contained 0.03% to 0.05% v/v tetramethylsilane, which was used as the reference signal (set at δ 0.00 for 1H).
LCMS analyses were performed on a SHIMADZU LCMS consisting of an UFLC 20-AD and LCMS 2020 MS detector. The column used was a Shim-pack XR-ODS, 2.2 μm, 3.0×50 mm. The instrument uses reverse-phase conditions (acetonitrile/water, containing 0.05% ammonia).
Abbreviations
Unless otherwise noted, or where the context dictates otherwise, the following abbreviations shall be understood to have the following meanings:
The assay was performed in a final volume of 9 μL in assay buffer containing 20 mM Tris-HCl (pH 8.0, (1M Tris-HCl, pH 8.0 solution; Corning 46-031-CM)), 1 mM GSH (L-glutathione reduced, Sigma-Aldrich, G4251-100G), 0.03% BGG (0.22 μM filtered, Sigma, G7516-25G), and 0.01% Triton X-100 (Sigma, T9284-10 L). Nanoliter quantities of 10-point, 3-fold serial dilution in DMSO were pre-dispensed into 1536 assay plates (Corning, #3724BC) for a final test concentration of 25 μM to 1.3 nM, top to lowest dose, respectively. Concentration and incubation times were optimized for the maximal signal-to-background while maintaining initial velocity conditions at a fixed substrate concentration. The final concentration of USP30 (human recombinant USP30, Boston Biochem, cat. #E-582) in the assay was 0.2 nM. Final substrate (Ub-Rh110; Ubiquitin-Rhodamine 110, UbiQ-126) concentration was 25 nM with [Ub-Rh110]<<Km. 3 μL of 2×USP30 was added to assay plates (pre-stamped with compound), preincubated for 30 minutes and then treated with 3 μL of 2×Ub-Rh110. Plates were incubated for 30 minutes at room temperature before addition of 3 μL of stop solution (final concentration of 10 mM citric acid (Sigma, 251275-500G)). Fluorescence was read on the Envision (excitation at 485 nm and emission at 535 nm; Perkin Elmer) or on the PheraSTAR (excitation at 485 nm and emission at 535 nm; BMG Labtech) fluorescence reader.
For all assay formats, data were reported as percent inhibition compared with control wells based on the following equation: % inh=1−((FLU−AveLow)/(AveHigh−AveLow)) where FLU=measured Fluorescence, AveLow=average Fluorescence of no enzyme control (n=16), and AveHigh=average Fluorescence of DMSO control (n=16). IC50 values were determined by curve fitting of the standard 4 parameter logistic fitting algorithm included in the Activity Base software package: IDBS XE Designer Mode1205. Data is fitted using the Levenburg Marquardt algorithm.
The calculated IC50 values of the compounds described herein are reported in Table 3, where A represents an IC50 of <0.1 μM, B represents an IC50 of 0.1 to 1.0 μM, and C represents an IC50 of >1.0 μM. Compounds in the USP30 biochemical assay were deemed active if the IC50 was ≤1 μM.
Compounds 1-a and 1-b were prepared by the following route:
2-Chloromethyl 2-(trimethylsilyl)ethyl ether (12.3 mL, 69.5 mmol) was added to a mixture of methyl 5-bromo-1H-pyrazole-3-carboxylate (5.00 g, 23.2 mmol) and K2CO3 (18.0 g, 130 mmol) in DMF (50 mL) at 0° C. in an ice/water bath. The resulting solution was stirred for 14 h at 25° C. The reaction was quenched by the addition of water (100 mL). The resulting mixture was extracted with ethyl acetate (3×100 mL). The combined organic layers were washed with brine (100 mL), dried over anhydrous sodium sulfate, filtered, and concentrated under vacuum. The residue was purified by silica gel chromatography (eluting with 15:1 petroleum ether/ethyl acetate) to afford methyl 5-bromo-1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-pyrazole-3-carboxylate as a yellow oil (6.20 g, 79%). LCMS (ES, m/z) 335, 337 [M+H]+.
A solution of methyl 5-bromo-1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-pyrazole-3-carboxylate (6.20 g, 18.4 mmol), (2-phenoxyphenyl)boronic acid (4.96 g, 23.2 mmol), XPhos-Pd (2.90 g, 3.68 mmol) and K3PO4 (11.7 g, 55.2 mmol) in dioxane (120 mL) and H2O (24 mL) was stirred for 15 h at 100° C. in an oil bath. After cooling to 25° C., the solids were filtered out. The filtrate was concentrated under vacuum. The residue was diluted with water (50 mL). The resulting mixture was extracted with ethyl acetate (3×50 mL). The combined organic layer was dried over anhydrous sodium sulfate, filtered, and concentrated under vacuum. The residue was purified by reverse phase chromatography (Column:)(Bridge Shield RP18 OBD Column, 5 μm, 30×150 mm; Mobile phase, A: water (containing 10 mmol/L NH4HCO3) and B: ACN (5% B to 72% over 20 min); Detector: UV:220 and 254 nm) to afford methyl 5-(2-phenoxyphenyl)-1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-pyrazole-3-carboxylate as a yellow solid (3.20 g, 41%). LCMS (ES, m/z) 425 [M+H]+.
A solution of methyl 5-(2-phenoxyphenyl)-1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-pyrazole-3-carboxylate (1.40 g, 3.30 mmol) and LiOH (0.810 g, 33.8 mmol) in THF (60 mL) and H2O (15 mL) was stirred for 4 h at 50° C. The mixture was allowed to cool to 25° C. and concentrated under vacuum. The pH value of the residue was adjusted to 5-6 with 3 N hydrochloric acid. The solids were collected by filtration and dried in an oven to afford 5-(2-phenoxyphenyl)-1-[[2-(trimethylsilyl)ethoxy] methyl]-1H-pyrazole-3-carboxylic acid as an off-white solid (1.05 g, 78%). LCMS (ES, m/z) 411 [M+H]+.
A solution of 5-(2-phenoxyphenyl)-1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-pyrazole-3-carboxylic acid (150 mg, 0.366 mmol), HATU (210 mg, 0.541 mmol), tert-butyl 2,6-diazabicyclo[3.2.1]octane-6-carboxylate (75.0 mg, 0.346 mmol) and DIEA (0.2 mL, 1.40 mmol) in DMF (2 mL) was stirred for 3 h at 25° C. The reaction was quenched by the addition of water (10 mL). The resulting mixture was extracted with ethyl acetate (3×20 mL). The combined organic layer was washed with brine (20 mL), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluting with 1/1 petroleum ether/ethyl acetate) to afford tert-butyl 2-[5-(2-phenoxyphenyl)-1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-pyrazole-3-carbonyl]-2,6-diazabicyclo[3.2.1]octane-6-carboxylate as a white solid (100 mg, 45%). LCMS (ES, m/z): 605 [M+H]+.
A solution of tert-butyl 2-[5-(2-phenoxyphenyl)-1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-pyrazole-3-carbonyl]-2,6-diazabicyclo[3.2.1]octane-6-carboxylate (100 mg, 0.157 mmol) and TFA (1 mL) in DCM (2 mL) was stirred for 2 h at 25° C. The resulting mixture was concentrated under vacuum to afford 2-[5-(2-phenoxyphenyl)-1H-pyrazole-3-carbonyl]-2,6-diazabicyclo[3.2.1]octane 2,2,2-trifluoroacetate as a colorless oil (110 mg, crude). LCMS (ES, m/z): 375 [M+H]+.
Cyanogen bromide (17.8 mg, 0.170 mmol) was added to a 0° C. mixture of 2-[5-(2-phenoxyphenyl)-1H-pyrazole-3-carbonyl]-2,6-diazabicyclo[3.2.1]octane 2,2,2-trifluoroacetate (80.0 mg, 0.170 mmol) and NaHCO3 (82.0 mg, 0.957 mmol) in DMF (2 mL). The resulting mixture stirred for 16 h at 25° C. The reaction was quenched by the addition of water (10 mL). The resulting mixture was extracted with ethyl acetate (3×20 mL). The combined organic layer was dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by Prep-HPLC (Column: XBridge Shield RP18 OBD Column, 5 μm,19×150 mm; Mobile Phase A: water (containing 10 mmol/L NH4HCO3) and B: CH3CN (30% to 55% in 8 min); Flow rate: 25 mL/min; Detector: 220 nm) to afford 2-[5-(2-phenoxyphenyl)-1H-pyrazole-3-carbonyl]-2,6-diazabicyclo[3.2.1]octane-6-carbonitrile as a white solid (40.0 mg, 59%). LCMS (ES, m/z): 400 [M+H]+.
2-[5-(2-Phenoxyphenyl)-1H-pyrazole-3-carbonyl]-2,6-diazabicyclo[3.2.1]octane-6-carbonitrile (40.0 mg, 0.100 mmol) was separated by chiral-HPLC (Column: CHIRAL ART Cellulose-SB, 2×25 cm, Sum; Mobile Phase A: n-hexane and B: EtOH (hold 50% in 15 min); Flow rate: 20 mL/min; Detector: 254/220 nm; RT1: 8.911 min and RT2: 11.119 min). The first eluting isomer (RT1=8.911 min) was collected and concentrated under vacuum, then lyophilized to obtain a compound for which the absolute stereochemistry was arbitrarily assigned as (1S,5R)-2-(5-(2-phenoxyphenyl)-1H-pyrazole-3-carbonyl)-2,6-diazabicyclo[3.2.1]octane-6-carbonitrile (1-a) as a white solid (13.8 mg, 35%). LCMS (ES, m/z): 400 [M+H]+; 1H-NMR (DMSO-d6, 400 MHz) δ (ppm): 13.63 (br s, 1H), 7.86-7.85 (m, 1H), 7.44-7.29 (m, 4H), 7.13-6.90 (m, 5H), 5.49-5.18 (m, 1H), 4.65-4.31 (m, 1H), 4.18-4.17 (m, 1H), 3.65-3.46 (m, 3H), 3.08-3.03 (m, 1H), 1.86-1.72 (m, 4H). The second eluting isomer (RT2=11.119 min) was collected and concentrated under vacuum, then lyophilized to obtain a compound for which the absolute stereochemistry was arbitrarily assigned as (1R,5S)-2-(5-(2-phenoxyphenyl)-1H-pyrazole-3-carbonyl)-2,6-diazabicyclo[3.2.1]octane-6-carbonitrile (1-b) as a white solid (14.8 mg, 37%). LCMS (ES, m/z): 400 [M+H]+; 1H-NMR (DMSO-d6, 400 MHz) δ (ppm): 13.63 (br s, 1H), 7.88-7.85 (m, 1H), 7.44-7.29 (m, 4H), 7.14-6.90 (m, 5H), 5.48-5.17 (m, 1H), 4.65-4.31 (m, 1H), 4.18-4.17 (m, 1H), 3.65-3.48 (m, 3H), 3.08-3.03 (m, 1H), 1.86-1. 72 (m, 4H).
The compounds set forth in Table 4 were prepared by methods analogous to the preparation of compounds 1-a and 1-b. Each pair of compounds listed in Table 4 (i.e., compounds 2-a and 2-b, compounds 3-a and 3-b, etc.) was obtained as a racemic mixture, and were then separated by chiral HPLC according to the procedure described in Example 2, Step 7, to obtain the individual compounds in substantially enantiomerically pure form. The first and second eluting enantiomer of each enantiomer pair is identified in Table 4. The absolute stereochemistry of each enantiomer was arbitrarily assigned.
1H-NMR
1HNMR (DMSO-d6, 400 MHz) δ (ppm): 13.7-13.6 (m, 1H), 8.42-8.15 (m, 1H), 8.04-7.85(m, 1H), 7.42-7.29 (m, 4H), 7.15-7.10 (m, 1H), 7.02-6.95 (m, 4H), 4.06-4.04 (m, 1H), 3.84-3.82 (m, 1H), 3.52-3.49 (m, 1H), 3.10-3.06 (m, 1H), 2.67-2.62 (m, 1H), 1.97-1.88 (m, 1H), 1.84-1.71 (m, 2H), 1.54-1.48 (m, 1H).
1HNMR (DMSO-d6, 400 MHz) δ (ppm): 13.8-13.6 (m, 1H), 8.57-8.15 (m, 1H), 8.02-7.86 (m, 1H), 7.40-7.22 (m, 4H), 7.15-7.11 (m, 1H), 7.01-6.97 (m, 4H), 4.06-4.04 (m, 1H), 3.83-3.81 (m, 1H), 3.53-3.50 (m, 1H), 3.09-3.06 (m, 1H), 2.71-2.60 (m, 1H), 1.97-1.88 (m, 1H), 1.84-1.71 (m, 2H), 1.54-1.48 (m, 1H).
1HNMR (DMSO-d6, 400 MHz) δ (ppm): 13.7 (br s, 1H), 7.91-7.89 (m, 1H), 7.44-7.37(m, 3H), 7.32-7.29 (m, 1H), 7.15-7.12 (m, 1H), 7.03-6.99 (m, 4H), 5.50-5.40 (m, 0.5H), 4.87-4.86 (m, 0.5H), 4.46-4.43 (m, 1H), 4.06-3.88 (m, 1H), 3.65-3.51 (m, 2H), 3.36-3.34 (m, 1H), 1.99-1.85 (m, 2H).
1HNMR (DMSO-d6, 400 MHz) δ (ppm): 13.7 (br s, 1H), 7.91-7.89 (m, 1H), 7.44-7.37(m, 3H), 7.32-7.29 (m, 1H), 7.15-7.12 (m, 1H), 7.03-6.99 (m, 4H), 5.50-5.40 (m, 0.5H), 4.87-4.86 (m, 0.5H), 4.46-4.43 (m, 1H), 3.99-3.88 (m, 1H), 3.65-3.51 (m, 2H), 3.44-3.34 (m, 1H), 1.99-1.81 (m, 2H).
1HNMR (DMSO-d6, 400 MHz) δ (ppm): 13.6 (br s, 1H), 8.41-8.38 (m, 1H), 7.92-7.85(m, 1H), 7.41-7.29 (m, 4H), 7.15-7.12 (m, 1H), 7.02-6.91 (m, 4H), 4.25-4.20 (m, 1H), 3.82-3.78 (m, 1H), 3.68-3.65 (m, 1H), 3.52-3.44 (m, 1H), 3.25-3.24 (m, 1H), 0.80-0.59 (m, 4H).
1HNMR (DMSO-d6, 400 MHz) δ (ppm): 13.6 (br s, 1H), 8.41-8.38 (m, 1H), 7.92-7.85(m, 1H), 7.41-7.29 (m, 4H), 7.15-7.12 (m, 1H), 7.02-6.91 (m, 4H), 4.25-4.20 (m, 1H), 3.82-3.78 (m, 1H), 3.68-3.65 (m, 1H), 3.48-3.40 (m, 1H), 3.26-3.24 (m, 1H), 0.80-0.59 (m, 4H).
1HNMR (DMSO-d6, 400 MHz) δ (ppm): 13.7-13.6 (m, 1H), 8.62-8.51 (m, 1H), 8.05-7.87 (m, 1H) 7.45-7.25 (m, 4H), 7.19-7.12 (m, 1H), 7.04-6.95 (m, 4H), 4.27-4.13 (m, 3H), 2.22-2.08 (m, 1H), 1.83-1.65 (m, 4H).
1HNMR (DMSO-d6, 400 MHz) δ (ppm): 13.7-13.6 (m, 1H), 8.62-8.51 (m, 1H), 8.03-7.86(m, 1H), 7.47-7.25 (m, 4H), 7.15-7.10 (m, 1H), 7.01-6.95 (m, 4H), 4.30-4.15 (m, 3H), 2.22-2.10 (m, 1H), 1.88-1.62 (m, 4H).
1HNMR (DMSO-d6, 400 MHz) δ (ppm): 13.7 (br s, 1H), 7.94-7.88 (m, 2H), 7.41-7.28 (m, 4H), 7.16-7.12 (m, 1H), 7.03-6.92 (m, 4H), 4.20-4.19 (m, 1H), 3.83-3.82 (m, 1H), 3.45-3.43 (m, 1H), 2.94-2.92 (m, 1H), 1.78-1.76 (m, 1H), 1.32-1.29 (m, 1H).
1HNMR (DMSO-d6, 400 MHz) δ (ppm): 13.6 (br s, 1H), 7.94-7.88 (m, 2H), 7.41-7.29 (m, 4H), 7.16-7.12 (m, 1H), 7.03-6.98 (m, 4H), 4.20-4.19 (m, 1H), 3.83-3.82 (m, 1H), 3.45-3.43 (m, 1H), 2.94-2.92 (m, 1H), 1.78-1.76 (m, 1H), 1.32-1.29 (m, 1H).
1H-NMR (CD3OD, 400 MHz) δ (ppm): 7.80-7.77 (m, 1H), 7.39-7.35 (m, 3H), 7.28-7.25 (m, 1H), 7.16-7.13 (m, 2H), 7.03-6.97 (m, 3H), 4.97-4.93 (m, 2H), 4.74-4.70 (m, 2H), 4.55-4.50 (m, 1H), 3.86-3.81 (m, 1H), 3.54-3.50 (m, 1H), 2.68-2.63 (m, 1H), 2.53-2.48 (m, 1H).
1H-NMR (CD30D, 400 MHz) δ (ppm): 7.80-7.77 (m, 1H), 7.39-7.35 (m, 3H), 7.28-7.25 (m, 1H), 7.16-7.13 (m, 2H), 7.03-6.97 (m, 3H), 4.97-4.90 (m, 2H), 4.74-4.70 (m, 2H), 4.55-4.51 (m, 1H), 3.86-3.82 (m, 1H), 3.54-3.50 (m, 1H), 2.68-2.63 (m, 1H), 2.53-2.48 (m, 1H).
1H-NMR (DMSO-d6, 400 MHz) δ (ppm): 1H-NMR (DMSO-d6, 400 MHz) δ (ppm): 13.75-13.61 (m, 1H), 8.55-8.20 (m, 1H), 8.05-7.87 (m, 1H), 7.45-7.30 (m, 4H), 7.16-7.14 (m, 1H), 7.03-6.97 (m, 3H), 6.95-6.85 (m, 1H), 4.80-4.77 (m, 1H), 3.72-3.67 (m, 1H), 3.51-3.49 (m, 1H), 3.12-3.08 (m, 1H), 1.90-1.80 (m, 1H), 1.40-1.20 (m, 1H), 0.75-0.60 (m, 1H).
1H-NMR (DMSO-d6, 400 MHz) δ (ppm): 13.70-13.58 (m, 1H), 8.55-8.21 (m, 1H), 8.03-7.86 (m, 1H), 7.45-7.13 (m, 5H), 7.04-6.92 (m, 3H), 3.70-3.66 (m, 2H), 3.54- 3.49 (m, 1H), 3.16-3.14 (m, 1H), 1.78-1.74 (m, 1H), 2.93-2.81 (m, 1H), 2.09- 1.90 (m, 3H), 1.71-1.63 (m, 2H), 1.41-1.37 (m, 1H).
1H-NMR (DMSO-d6, 400 MHz) δ (ppm): 13.62 (br s, 1H), 8.33 (br s, 1H), 7.94- 7.93 (m, 1H), 7.42-7.30 (m, 3H), 7.28-7.26 (m, 1H), 7.16-7.14 (m, 1H), 7.12 (br s, 1H), 7.08-6.98 (m, 3H), 3.70-3.64 (m, 2H), 3.52-3.50 (m, 1H), 3.16-3.13 (m, 1H), 2.91-2.89 (m, 1H), 2.05- 1.89 (m, 3H), 1.73-1.63 (m, 2H), 1.41-1.37 (m, 1H).
Compounds 6-a and 6-b were prepared by the following route:
2-(Trimethylsilyl)ethoxymethyl chloride (12.2 mL, 68.8 mmol) was added dropwise to a 0° C. solution of methyl 5-bromo-1H-pyrazole-3-carboxylate (5.00 g, 24.5 mmol) and potassium carbonate (18.0 g, 130 mmol) in DMF (10 mL). The resulting mixture was stirred for 14 h at 25° C. The reaction was quenched with water (20 mL) at 0° C. The resulting mixture was extracted with ethyl acetate (3×30 mL). The combined organic layers were washed with brine (2×100 mL), dried over anhydrous sodium sulfate, and filtered. The filtrate was concentrated under vacuum. The residue was purified by silica gel chromatography (eluting with 15:1 petroleum ether/ethyl acetate) to afford methyl 5-bromo-1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-pyrazole-3-carboxylate (6.20 g, 76%) as a yellow oil. LCMS (ES, m/z): 335, 337 [M+H]+.
A solution of methyl 5-bromo-1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-pyrazole-3-carboxylate (6.20 g, 18.5 mmol), (2-phenoxyphenyl)boronic acid (4.96 g, 23.2 mmol), XPhos-Pd-G3 (3.12 g, 36.9 mmol) and potassium phosphate tribasic (25.4 mg, 37.1 mmol) in dioxane (120 mL) and water (24 mL) was stirred for 15 h at 100° C. in an oil bath. The mixture was cooled to 25° C. The resulting mixture was concentrated under vacuum. The residue was diluted with water (30 mL). The resulting mixture was extracted with ethyl acetate (3×30 mL). The combined organic layers were dried over anhydrous sodium sulfate, filtered, and concentrated. The residue was purified by reverse phase chromatography (Column:)(Bridge Shield RP18 OBD Column, 5 μm, 30×150 mm; Mobile phase, A: water (containing 0.05% ammonium hydrogen) and B: acetonitrile (5% B to 72% over 20 min); Detector: UV 220 and 254 nm) to afford methyl 5-(2-phenoxyphenyl)-1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-pyrazole-3-carboxylate as a yellow solid (3.20 g, 41%). LCMS (ES, m/z): 425 [M+H]+.
A solution of methyl 5-(2-phenoxyphenyl)-1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-pyrazole-3-carboxylate (1.40 g, 3.30 mmol) and lithium hydroxide (810 mg, 34.0 mmol) in THF (60.0 mL), water (15.0 mL), and methanol (30.0 mL) was stirred for 4 h at 50° C. The mixture was cooled to 25° C. and concentrated under vacuum. The pH value of the residue was adjusted to 3-4 with 3 N aqueous hydrochloric acid solution. The resulting mixture was extracted with ethyl acetate (3×30 mL). The combined organic layers were washed with brine (2×100 mL), dried over anhydrous sodium sulfate, filtered, and concentrated. The residue was purified by silica gel chromatography (eluting with 2:1 petroleum ether/ethyl acetate) to afford 5-(2-phenoxyphenyl)-1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-pyrazole-3-carboxylic acid as an off-white solid (1.00 g, 74%). LCMS (ES, m/z): 411 [M+H]+.
A solution of 5-(2-phenoxyphenyl)-1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-pyrazole-3-carboxylic acid (300 mg, 0.723 mmol), tert-butyl 1-amino-3-azabicyclo[3.2.0]heptane-3-carboxylate (154 mg, 0.723 mmol), HATU (275 mg, 0.723 mmol) and N,N-diisopropylethylamine (0.239 mL, 1.45 mmol) in DMF (2 mL) was stirred for 40 min at 25° C. The reaction was quenched with water (5 mL). The resulting mixture was extracted with ethyl acetate (3×15 mL). The combined organic layers were washed with brine (2×30 mL), dried over anhydrous sodium sulfate, filtered, and concentrated. The residue was purified by silica gel chromatography (eluting with 4:1 petroleum ether/ethyl acetate) to afford tert-butyl 1-(5-(2-phenoxyphenyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazole-3-carboxamido)-3-azabicyclo[3.2.0]heptane-3-carboxylate as an off-white solid (350 mg, 80%). LCMS (ES, m/z): 605 [M+H]+.
A solution of tert-butyl 1-(5-(2-phenoxyphenyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazole-3-carboxamido)-3-azabicyclo[3.2.0]heptane-3-carboxylate (350 mg, 0.579 mmol) in trifluoroacetic acid (1 mL) and dichloromethane (3 mL) was stirred for 30 min at 25° C. The resulting mixture was concentrated under vacuum to afford N-(3-azabicyclo[3.2.0]heptan-1-yl)-5-(2-phenoxyphenyl)-1H-pyrazole-3-carboxamide 2,2,2-trifluoroacetate as a brown oil (360 mg, crude). LCMS (ES, m/z): 375 [M+H]t
Cyanogen bromide (72.8 mg, 0.687 mmol) was added dropwise to a 0° C. solution of N-(3-azabicyclo[3.2.0]heptan-1-yl)-5-(2-phenoxyphenyl)-1H-pyrazole-3-carboxamide 2,2,2-trifluoroacetate (350 mg, 0.763 mmol) and sodium bicarbonate (785 mg, 9.25 mmol) in DMF (2 mL). The mixture was stirred for 1 h at 25° C. The solids were filtered out. The filtrate was directly purified by Prep-HPLC (Column:)(Bridge Shield RP18 OBD Column, 5 μm, 30×150 mm; Mobile phase, A: water (containing 0.05% ammonium hydrogen) and B: acetonitrile (35% B to 65% over 7 min); Detector: UV 220 and 254 nm) to afford N-(3-cyano-3-azabicyclo[3.2.0]heptan-1-yl)-5-(2-phenoxyphenyl)-1H-pyrazole-3-carboxamide as a white solid (70.0 mg). This material was separated by chiral-HPLC (Column: Chiralpak IG, 2*25 cm, 5 μm; Mobile Phase, A: MTBE and B: EtOH (hold 15% in 24 min); Flow rate: 20 mL/min; Detector: 220/254 nm). The first eluting isomer was collected, and the absolute stereochemistry was arbitrarily assigned as (1R,5S): N-((1R,5S)-3-cyano-3-azabicyclo[3.2.0]heptan-1-yl)-5-(2-phenoxyphenyl)-1H-pyrazole-3-carboxamide (RT1=10.9 min) as a white solid (6-a, 28.5 mg, 10%). LCMS (ES, m/z): 400 [M+H]+. 1H-NMR (DMSO-d6, 400 MHz) δ (ppm): 13.68-13.62 (m, 1H), 8.92-8.61 (m, 1H), 8.03-7.86 (m, 1H), 7.42-7.23 (m, 4H), 7.21-7.12 (m, 1H), 7.03-6.89 (m, 4H), 3.73-3.70 (m, 1H), 3.68-3.56 (m, 1H), 3.39-3.31 (m, 2H), 3.08-3.05 (m, 1H), 2.34-2.31 (m, 1H), 2.20-2.08 (m, 2H), 1.61-1.58 (m, 1H). The second eluting isomer was collected, and the absolute stereochemistry was arbitrarily assigned as (1S,5R): N-((1S,5R)-3-cyano-3-azabicyclo[3.2.0]heptan-1-yl)-5-(2-phenoxyphenyl)-1H-pyrazole-3-carboxamide (RT2=12.7 min) as a white solid (6-b, 20.6 mg, 8%). LCMS (ES, m/z): 400 [M+H]+. 1H-NMR (DMSO-d6, 400 MHz) δ (ppm): 13.68-13.62 (m, 1H), 8.92-8.61 (m, 1H), 8.03-7.86 (m, 1H), 7.42-7.29 (m, 4H), 7.21-7.12 (m, 1H), 7.04-6.89 (m, 4H), 3.73-3.70 (m, 1H), 3.68-3.54 (m, 1H), 3.39-3.31 (m, 2H), 3.08-3.05 (m, 1H), 2.34-2.31 (m, 1H), 2.20-2.08 (m, 2H), 1.61-1.58 (m, 1H). Alternatively, the absolute stereochemistry of the first and second eluting isomers could have been arbitrarily assigned as (1S,5R) and (1R,5S), respectively.
Compounds 3-a and 3-b were prepared by the following route:
2-(Trimethylsilyl)ethoxymethyl chloride (12.2 mL, 68.8 mmol) was added dropwise to a 0° C. solution of methyl 5-bromo-1H-pyrazole-3-carboxylate (5.00 g, 24.5 mmol) and potassium carbonate (18.0 g, 130 mmol) in DMF (10 mL). The resulting mixture stirred for 14 h at 25° C. The reaction was quenched with water (20 mL) at 0° C. The resulting mixture was extracted with ethyl acetate (3×30 mL). The combined organic layers were washed with brine (2×100 mL), dried over anhydrous sodium sulfate, and filtered. The filtrate was concentrated under vacuum. The residue was purified by silica gel chromatography (eluting with 15:1 petroleum ether/ethyl acetate) to afford methyl 5-bromo-1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-pyrazole-3-carboxylate (6.20 g, 76%) as a yellow oil. LCMS (ES, m/z): 335, 337 [M+H]+.
A solution of methyl 5-bromo-1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-pyrazole-3-carboxylate (6.20 g, 18.5 mmol), (2-phenoxyphenyl)boronic acid (4.96 g, 23.2 mmol), XPhos-Pd-G3 (3.12 g, 36.9 mmol) and potassium phosphate tribasic (25.4 mg, 37.1 mmol) in dioxane (120 mL) and water (24 mL) was stirred for 15 h at 100° C. in an oil bath. The mixture was cooled to 25° C. The resulting mixture was concentrated under vacuum. The residue was diluted with water (30 mL). The resulting mixture was extracted with ethyl acetate (3×30 mL). The combined organic layers were dried over anhydrous sodium sulfate, filtered, and concentrated. The residue was purified by reverse phase chromatography (Column:)(Bridge Shield RP18 OBD Column, 5 μm, 30×150 mm; Mobile phase, A: water (containing 0.05% ammonium hydrogen) and B: acetonitrile (5% B to 72% over 20 min); Detector: UV 220 and 254 nm) to afford methyl 5-(2-phenoxyphenyl)-1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-pyrazole-3-carboxylate as a yellow solid (3.20 g, 41%). LCMS (ES, m/z): 425 [M+H]+.
A solution of methyl 5-(2-phenoxyphenyl)-1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-pyrazole-3-carboxylate (1.40 g, 3.30 mmol) and lithium hydroxide (810 mg, 34.0 mmol) in THF (60.0 mL), water (15.0 mL), and methanol (30.0 mL) was stirred for 4 h at 50° C. The mixture was cooled to 25° C. and concentrated under vacuum. The pH value of the residue was adjusted to 3-4 with 3 N aqueous hydrochloric acid solution. The resulting mixture was extracted with ethyl acetate (3×30 mL). The combined organic layers were washed with brine (2×100 mL), dried over anhydrous sodium sulfate, filtered, and concentrated. The residue was purified by silica gel chromatography (eluting with 2:1 petroleum ether/ethyl acetate) to afford 5-(2-phenoxyphenyl)-1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-pyrazole-3-carboxylic acid as an off-white solid (1.00 g, 74%). LCMS (ES, m/z): 411 [M+H]+.
A solution of 5-(2-phenoxyphenyl)-1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-pyrazole-3-carboxylic acid (300 mg, 0.723 mmol), tert-butyl 1-amino-3-azabicyclo[3.1.0]hexane-3-carboxylate (145 mg, 0.723 mmol), HATU (278 mg, 0.723 mmol) and N,N-diisopropylethylamine (0.242 mL, 1.47 mmol) in DMF (3 mL) was stirred for 30 min at 25° C. The reaction was quenched with water (10 mL) at 25° C. The resulting mixture was extracted with ethyl acetate (3×10 mL). The combined organic layers were washed with brine (2×30 mL), dried over anhydrous sodium sulfate, filtered, and concentrated. The residue was purified by silica gel chromatography (eluting with 4:1 petroleum ether/ethyl acetate) to afford tert-butyl 1-(5-(2-phenoxyphenyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazole-3-carboxamido)-3-azabicyclo[3.1.0]hexane-3-carboxylate as an off-white solid (280 mg, 67%). LCMS (ES, m/z): 591 [M+H]+.
A solution of tert-butyl 1-(5-(2-phenoxyphenyl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazole-3-carboxamido)-3-azabicyclo[3.1.0]hexane-3-carboxylate (280 mg, 0.475 mmol) in trifluoroacetic acid (1 mL) and dichloromethane (3 mL) was stirred for 2 h at 25° C. The resulting mixture was concentrated under vacuum to afford N-(3-azabicyclo[3.1.0]hexan-1-yl)-5-(2-phenoxyphenyl)-1H-pyrazole-3-carboxamide 2,2,2-trifluoroacetate as a yellow oil (285 mg, crude). LCMS (ES, m/z): 361 [M+H]+.
Cyanogen bromide (58.5 mg, 0.552 mmol) was added dropwise to a 0° C. solution of N-(3-azabicyclo[3.1.0]hexan-1-yl)-5-(2-phenoxyphenyl)-1H-pyrazole-3-carboxamide 2,2,2-trifluoroacetate (280 mg, 0.613 mmo1) and sodium bicarbonate (653 mg, 7.69 mmol) in DMF (2 mL). The mixture was stirred for 1 h at 25° C. The reaction was cooled to 0° C. and quenched with water (10 mL). The resulting mixture was extracted with ethyl acetate (3×10 mL). The combined organic layers were washed with brine (20 mL), dried over anhydrous sodium sulfate, filtered, and concentrated. The residue was purified by Prep-HPLC (Column:)(Bridge Shield RP18 OBD Column, 5 μm, 30×150 mm; Mobile phase, A: water (containing 0.05% ammonium hydrogen) and B: acetonitrile (28% B to 48% over 7 min); Detector: UV 220 and 254 nm) to afford N-(3-cyano-3-azabicyclo[3.1.0]hexan-1-yl)-5-(2-phenoxyphenyl)-1H-pyrazole-3-carboxamide as a white solid (60.0 mg). This material was separated by chiral-HPLC (Column: Chiralpak IG, 2*25 cm, 5 μm; Mobile Phase, A: MTBE and B: EtOH (hold 30% in 10.5 min); Flow rate: 13 mL/min; Detector: 220/254 nm). The first eluting isomer was collected, and the absolute stereochemistry was arbitrarily assigned as (1S,5R): N-((1S,5R)-3-cyano-3-azabicyclo[3.1.0]hexan-1-yl)-5-(2-phenoxyphenyl)-1H-pyrazole-3-carboxamide (RT1=6.45 min) as a pink solid (3-a, 30.3 mg, 14%). LCMS (ES, m/z): 386 [M+H]+. 1H-NMR (DMSO-d6, 400 MHz) δ (ppm): 13.72-13.64 (m, 1H), 9.08-8.70 (m, 1H), 8.05-7.85 (m, 1H), 7.44-7.29 (m, 4H), 7.20-7.12 (m, 1H), 7.04-6.87 (m, 4H), 3.69-3.66 (m, 1H), 3.57-3.48 (m, 3H), 1.78-1.74 (m, 1H), 1.17-1.14 (m, 1H), 0.87-0.82 (m, 1H). The second eluting isomer was collected, and the absolute stereochemistry was arbitrarily assigned as (1R,5S); N-((1R,5S)-3-cyano-3-azabicyclo[3.1.0]hexan-1-yl)-5-(2-phenoxyphenyl)-1H-pyrazole-3-carboxamide (RT2=8.97 min) (3-b, 29.9 mg, 14%) as a white solid. LCMS (ES, m/z): 386 [M+H]+. 1H-NMR (DMSO-d6, 400 MHz) δ (ppm): 13.72-13.64 (m, 1H), 9.08-8.70 (m, 1H), 8.05-7.85 (m, 1H), 7.44-7.29 (m, 4H), 7.22-7.12 (m, 1H), 7.04-6.87 (m, 4H), 3.69-3.66 (m, 1H), 3.57-3.51 (m, 3H), 1.78-1.74 (m, 1H), 1.17-1.14 (m, 1H), 0.87-0.82 (m, 1H). Alternatively, the absolute stereochemistry of the first and second eluting isomers could have been arbitrarily assigned as (1R,5S) and (1S,5R), respectively.
Many modifications and variations of the embodiments described herein may be made without departing from the scope, as is apparent to those skilled in the art. The specific embodiments described herein are offered by way of example only.
The present application is a U.S. National Stage Application of PCT/US19/54803, filed Oct. 4, 2019, which claims priority to U.S. Provisional Patent Application No. 62/741,945, filed Oct. 5, 2018, the entire contents of each of which are hereby incorporated by reference.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/US2019/054803 | 10/4/2019 | WO |
| Publishing Document | Publishing Date | Country | Kind |
|---|---|---|---|
| WO2020/072964 | 4/9/2020 | WO | A |
| Number | Name | Date | Kind |
|---|---|---|---|
| 6376515 | Zhu et al. | Apr 2002 | B2 |
| 6576632 | Goldstein et al. | Jun 2003 | B1 |
| 6632815 | Zhu et al. | Oct 2003 | B2 |
| 6835727 | Okamoto et al. | Dec 2004 | B2 |
| 7425354 | Yanai et al. | Sep 2008 | B2 |
| 7687504 | Jiaang et al. | Mar 2010 | B2 |
| 7807691 | Gavardinas et al. | Oct 2010 | B2 |
| 7910741 | Nishizawa et al. | Mar 2011 | B2 |
| 8329708 | Sim et al. | Dec 2012 | B2 |
| 8815924 | Dorsch et al. | Aug 2014 | B2 |
| 9393244 | Moussa | Jul 2016 | B2 |
| 9511142 | Burns et al. | Dec 2016 | B2 |
| 9550792 | Lu et al. | Jan 2017 | B2 |
| 9926307 | Jones et al. | Mar 2018 | B2 |
| 9938272 | Ding et al. | Apr 2018 | B2 |
| 9997717 | Kawamura et al. | Jun 2018 | B2 |
| 10590109 | Kong et al. | Mar 2020 | B2 |
| 10615343 | Stoessel et al. | Apr 2020 | B2 |
| 11247987 | Caravella et al. | Feb 2022 | B2 |
| 20030191279 | Goldstein et al. | Oct 2003 | A1 |
| 20090264499 | Deng et al. | Oct 2009 | A1 |
| 20160264548 | Qiu et al. | Sep 2016 | A1 |
| 20170247365 | Jones et al. | Aug 2017 | A1 |
| 20180228923 | Lai et al. | Aug 2018 | A1 |
| 20200317658 | Caravella et al. | Oct 2020 | A1 |
| 20210198263 | Martin et al. | Jul 2021 | A1 |
| 20220185806 | Caravella et al. | Jun 2022 | A1 |
| Number | Date | Country |
|---|---|---|
| 101838264 | Sep 2010 | CN |
| 104045552 | Sep 2014 | CN |
| 104557862 | Apr 2015 | CN |
| 106986859 | Jul 2017 | CN |
| 107619384 | Jan 2018 | CN |
| 102004054666 | May 2006 | DE |
| 3590931 | Jan 2020 | EP |
| 2424881 | Oct 2006 | GB |
| 2009108152 | May 2009 | JP |
| 2009149754 | Jul 2009 | JP |
| 2010066630 | Mar 2010 | JP |
| 2011006360 | Jan 2011 | JP |
| 2011042606 | Mar 2011 | JP |
| 2012123292 | Jun 2012 | JP |
| 5057056 | Oct 2012 | JP |
| 5219583 | Jun 2013 | JP |
| 5443720 | Mar 2014 | JP |
| 2014232188 | Dec 2014 | JP |
| 5899607 | Apr 2016 | JP |
| 1077417 | Oct 2011 | KR |
| 1715090 | Mar 2017 | KR |
| WO-2001019788 | Mar 2001 | WO |
| WO-2001019798 | Mar 2001 | WO |
| WO-2001029007 | Apr 2001 | WO |
| WO-2001064642 | Sep 2001 | WO |
| WO-2001064643 | Sep 2001 | WO |
| WO-2001077073 | Oct 2001 | WO |
| WO-2002046159 | Jun 2002 | WO |
| WO-2002051831 | Jul 2002 | WO |
| WO-2003007955 | Jan 2003 | WO |
| WO-2003020217 | Mar 2003 | WO |
| WO-2004002481 | Jan 2004 | WO |
| WO-2004014370 | Feb 2004 | WO |
| WO-2004014902 | Feb 2004 | WO |
| WO-2004080966 | Sep 2004 | WO |
| WO-2004085385 | Oct 2004 | WO |
| WO-2004110350 | Dec 2004 | WO |
| WO-2005000300 | Jan 2005 | WO |
| WO-2005019200 | Mar 2005 | WO |
| WO-2005044797 | May 2005 | WO |
| WO-2005077345 | Aug 2005 | WO |
| WO-2005077368 | Aug 2005 | WO |
| WO-2005077373 | Aug 2005 | WO |
| WO-2005080379 | Sep 2005 | WO |
| WO-2005112540 | Dec 2005 | WO |
| WO-2005115374 | Dec 2005 | WO |
| WO-2005115382 | Dec 2005 | WO |
| WO-2006014185 | Feb 2006 | WO |
| WO-2006015279 | Feb 2006 | WO |
| WO-2006024034 | Mar 2006 | WO |
| WO-2006027076 | Mar 2006 | WO |
| WO-2006045350 | May 2006 | WO |
| WO-2006063113 | Jun 2006 | WO |
| WO-2006074445 | Jul 2006 | WO |
| WO-2006076202 | Jul 2006 | WO |
| WO-2006113261 | Oct 2006 | WO |
| WO-2006129199 | Dec 2006 | WO |
| WO-2007024744 | Mar 2007 | WO |
| WO-2007061923 | May 2007 | WO |
| WO-2007144202 | Dec 2007 | WO |
| WO-2007144204 | Dec 2007 | WO |
| WO-2007146838 | Dec 2007 | WO |
| WO-2008028553 | Mar 2008 | WO |
| WO-2008035209 | Mar 2008 | WO |
| WO-2008071456 | Jun 2008 | WO |
| WO-2008073670 | Jun 2008 | WO |
| WO-2008079291 | Jul 2008 | WO |
| WO-2008141976 | Nov 2008 | WO |
| WO-2009010156 | Jan 2009 | WO |
| WO-2009011850 | Jan 2009 | WO |
| WO-2009047105 | Apr 2009 | WO |
| WO-2009078992 | Jun 2009 | WO |
| WO-2009089042 | Jul 2009 | WO |
| WO-2009129371 | Oct 2009 | WO |
| WO-2009158571 | Dec 2009 | WO |
| WO-2010048149 | Apr 2010 | WO |
| WO-2010075376 | Jul 2010 | WO |
| WO-2011025706 | Mar 2011 | WO |
| WO-2011031934 | Mar 2011 | WO |
| WO-2011053825 | May 2011 | WO |
| WO-2011103091 | Aug 2011 | WO |
| WO-2011126903 | Oct 2011 | WO |
| WO-2011143495 | Nov 2011 | WO |
| WO-2011161446 | Dec 2011 | WO |
| WO-2012016217 | Feb 2012 | WO |
| WO-2012078855 | Jun 2012 | WO |
| WO-2012083048 | Jun 2012 | WO |
| WO-2012083059 | Jun 2012 | WO |
| WO-2012129562 | Sep 2012 | WO |
| WO-2012139425 | Oct 2012 | WO |
| WO-2012160015 | Nov 2012 | WO |
| WO-2012166951 | Dec 2012 | WO |
| WO-2012177782 | Dec 2012 | WO |
| WO-2012177997 | Dec 2012 | WO |
| WO-2013046136 | Apr 2013 | WO |
| WO-2013052845 | Apr 2013 | WO |
| WO-2013086229 | Jun 2013 | WO |
| WO-2013106678 | Jul 2013 | WO |
| WO-2013130890 | Sep 2013 | WO |
| WO-2013132991 | Sep 2013 | WO |
| WO-2013178816 | Dec 2013 | WO |
| WO-2013182274 | Dec 2013 | WO |
| WO-2013190212 | Dec 2013 | WO |
| WO-2014000846 | Jan 2014 | WO |
| WO-2014041111 | Mar 2014 | WO |
| WO-2014068527 | May 2014 | WO |
| WO-2014072261 | May 2014 | WO |
| WO-2014108053 | Jul 2014 | WO |
| WO-2014140059 | Sep 2014 | WO |
| WO-2014159733 | Oct 2014 | WO |
| WO-2014165232 | Oct 2014 | WO |
| WO-2015003816 | Jan 2015 | WO |
| WO-2015010297 | Jan 2015 | WO |
| WO-2015011284 | Jan 2015 | WO |
| WO-2015048547 | Apr 2015 | WO |
| WO-2015048662 | Apr 2015 | WO |
| WO-2015058832 | Apr 2015 | WO |
| WO-2015085238 | Jun 2015 | WO |
| WO-2015095104 | Jun 2015 | WO |
| WO-2015106292 | Jul 2015 | WO |
| WO-2015130790 | Sep 2015 | WO |
| WO-2015173225 | Nov 2015 | WO |
| WO-2015176625 | Nov 2015 | WO |
| WO-2015189646 | Dec 2015 | WO |
| WO-2015197028 | Dec 2015 | WO |
| WO-2016007534 | Jan 2016 | WO |
| WO-2016008011 | Jan 2016 | WO |
| WO-2016016366 | Feb 2016 | WO |
| WO-2016034262 | Mar 2016 | WO |
| WO-2016040449 | Mar 2016 | WO |
| WO-2016046530 | Mar 2016 | WO |
| WO-2016109559 | Jul 2016 | WO |
| WO-2016156816 | Oct 2016 | WO |
| WO-2016172631 | Oct 2016 | WO |
| WO-2017002120 | Jan 2017 | WO |
| WO-2017009650 | Jan 2017 | WO |
| WO-2017010399 | Jan 2017 | WO |
| WO-2017019817 | Feb 2017 | WO |
| WO-2017019822 | Feb 2017 | WO |
| WO-2017019830 | Feb 2017 | WO |
| WO-2017040194 | Mar 2017 | WO |
| WO-2017040982 | Mar 2017 | WO |
| WO-2017066705 | Apr 2017 | WO |
| WO-2017093718 | Jun 2017 | WO |
| WO-2017100558 | Jun 2017 | WO |
| WO-2017103614 | Jun 2017 | WO |
| WO-2017109488 | Jun 2017 | WO |
| WO-2017141036 | Aug 2017 | WO |
| WO-2017149313 | Sep 2017 | WO |
| WO-2017158381 | Sep 2017 | WO |
| WO-2017158388 | Sep 2017 | WO |
| WO-2017161028 | Sep 2017 | WO |
| WO-2017162007 | Sep 2017 | WO |
| WO-2017163078 | Sep 2017 | WO |
| WO-2018005591 | Jan 2018 | WO |
| WO-2018010514 | Jan 2018 | WO |
| WO-2018024188 | Feb 2018 | WO |
| WO-2018039896 | Mar 2018 | WO |
| WO-2018060689 | Apr 2018 | WO |
| WO-2018060691 | Apr 2018 | WO |
| WO-2018060742 | Apr 2018 | WO |
| WO-2018065768 | Apr 2018 | WO |
| WO-2018106818 | Jun 2018 | WO |
| WO-2018106820 | Jun 2018 | WO |
| WO-2018134352 | Jul 2018 | WO |
| WO-2018146116 | Aug 2018 | WO |
| WO-2018157856 | Sep 2018 | WO |
| WO-2018160891 | Sep 2018 | WO |
| WO-2018213150 | Nov 2018 | WO |
| WO-2018220355 | Dec 2018 | WO |
| WO-2018234775 | Dec 2018 | WO |
| WO-2019071073 | Apr 2019 | WO |
| WO-2019171042 | Sep 2019 | WO |
| WO-2019222468 | Nov 2019 | WO |
| WO-2020036940 | Feb 2020 | WO |
| WO-2020072964 | Apr 2020 | WO |
| WO-2020212350 | Oct 2020 | WO |
| WO-2020212351 | Oct 2020 | WO |
| WO-2021043870 | Mar 2021 | WO |
| WO-2021050992 | Mar 2021 | WO |
| Entry |
|---|
| Ahmed, H.E.A. and Bajorath, J., Methods for Computer-Aided Chemical Biology, Part 5: Rationalizing the Selectivity of Cathepsin Inhibitors on the Basis of Molecular Fragments and Topological Feature Distributions, Chemical Biology & Drug Design, (74): 129-141 (2009). |
| Bingol, B. et al., The mitochondrial deubiquitinase USP30 opposes parkin—mediated mitophagy, Nature, 510:370-375 (2014). |
| Buus, R. et al., Deubiquitinase Activities Required for Hepatocyte Growth Factor-Induced Scattering of Epithelial Cells, Current Bio., 19:1463-1466 (2009). |
| Dovlatyan, M. et al., A High-Content Live Imaging Mitophagy Assay to Evaluate Small Molecule Mitophagy Enhancers, Poster Abstract (Board No. B555) presented at ASCB EMBO (Dec. 2017). |
| Durcan, T. M. and Edward, A. F., The three ‘P’s of mitophagy: PARKIN, PINK1, and post-translational modifications, Genes and Development, 29:989-999 (2015). |
| International Search Report for PCT/US2018/054520, 4 pages (dated Feb. 5, 2019). |
| International Search Report for PCT/US2019/032619, 5 pages (dated Jul. 16, 2019). |
| International Search Report for PCT/US2019/054803, 6 pages (dated Nov. 27, 2019). |
| Iwashita, H. et al., Live Cell Imaging of Mitochondrial Autophagy with a Novel Fluorescent Small Molecule, ACS Chem. Biol., 12:2546-2551 (2017). |
| Ji, Y. et al., Innate C-H Trifluoromethylation of Heterocycles, PNAS, 108(35):14411-14415 (2011). |
| Kluge, A. F. et al., Novel Highly Selective Inhibitors of Ubiquitin Specific Protease 30 (USP30) Accelerate Mitophagy, Bioorg. and Medic. Chem. Lett., 28(15):2655-2659 (2018). |
| Lainé, D., et al., Discovery of Novel Cyanamide-Based Inhibitors of Cathepsin C, ACS Med. Chem. Lett., 2:142-147 (2011). |
| McWilliams, T. G. et al., mit-QC illuminates mitophagy and mitochondrial architecture in vivo, J. Cell Biol., 214:333-345 (2016). |
| Nakamura, N. and Hirose, S., Regulation of Mitochondrial Morphology by USP30, a Deubiquitinating Enzyme Present in the Mitochondrial Outer Membrane, Mole. Bio. Cell., 19:1903-1911 (2008). |
| Ndubaku, C. and Tsui, V., Inhibiting the Deubiquitinating Enzymes (DUBs), Jrnl. Med. Chem., 58:1581-1595 (2015). |
| Pollock, S.R., and Kashatus, D.F., A novel role for RalA during PINK1-Parkin mitophagy, Poster Abstract (Board No. B3252) presented at ASCB EMBO (Dec. 2017). |
| PubChem CID 116045277, (3-Methylcyclobutyl)cyanamide, 2 pages, Date Created: Jan. 30, 2016, Date Modified: Aug. 8, 2020. |
| PubChem CID 116214356, (1-Ethylcyclobutyl)cyanamide, 2 pages, Date Created: Jan. 30, 2016, Date Modified: Aug. 8, 2020. |
| PubChem CID 21516572, (1-Methylcyclopropyl)cyanamide, 7 pages, Date Created: Dec. 5, 2007, Date Modified: Apr. 18, 2020. |
| Puri, R. et al., Mitochondrial Ubiquitin Ligase Mul1 Mediates an Early Stress Protection of Neuronal Mitochondria From Degradation by Parkin-Mediated Mitophagy, Poster Abstract (Board No. B482) presented at ASCB EMBO (Dec. 2017). |
| Rusilowicz-Jones, E. et al., A novel USP30 inhibitor recapitulates genetic loss of USP30 and sets the trigger for PINK1-PARKIN amplicfication of mitochondrial ubiquitylation, bioRxiv, doi: https://doi.org/10.1101/2020.04.16.044206, 1-35 (posted Apr. 20, 2020). |
| Rusilowicz-Jones, E. et al., USP30 sets a trigger threshold for PINK1-PARKIN amplification of mitochondrial ubiquitylation, Life Sci. Alli., 3(8):1-14 (2020). |
| Rusilowicz-Jones, E. V. et al., Benchmarking a highly selective USP30 inhibitor for enhancement of mitophagy and pexophagy, bioRxiv, doi:https://doi.org/10.1101/2021.04.28.441730, 1-19 (posted Apr. 28, 2021). |
| Sathe, M. et al., Efficient synthesis of N-cyano α and β-amino esters, Synthetic Communications: An International Journal for Rapid Communication of Synthetic Organic Chemistry, 38: 1375-1380 (2008). |
| Seiberlich, V. et al., The small molecule inhibitor PR-619 of deubiquitinating enzymes affects the microtubule network and causes protein aggregate formation in neural cells: Implications for neurodegenerative diseases, Biochem Biophys Acta., 1823 (11):2057-2068 (2012). |
| Silverman, R., “The Organic Chemistry of Drug Design and Drug Action”, NY Elsevier, 29-32 (2004). |
| Thompson, J. E. et al., Discovery of MF-0094, a potent, selective and cell permeable inhibitor of USP30, Poster (2017). |
| Deaton, D. N. et al., Novel and potent cyclic cyanamide-based cathepsin K inhibitors, Bioorg. Med. Chem. Lett., 15:1815-1819 (2005). |
| Number | Date | Country | |
|---|---|---|---|
| 20210355126 A1 | Nov 2021 | US |
| Number | Date | Country | |
|---|---|---|---|
| 62741945 | Oct 2018 | US |
