Patent Application
20230202974
Caspase 6 is an enzyme that in humans is encoded by the CASP6 gene. Caspase 6 has known functions in apoptosis, early immune response and neurodegeneration in Huntington’s and Alzheimer’s disease. Identifying inhibitors of Caspase 6 has proven to be a challenge. Disclosed herein, inter alia, are solutions to these and other problems known in the art.
In an aspect is provided a compound having the formula:
or
R1 is independently halogen, —CX13, —CHX12, —CH2X1, —OCX13, —OCH2X1, —OCHX12, —CN, —SOn1R1D, —SOv1NR1AR1B, —NR1CNR1AR1B, —ONR1AR1B, —NHC(O)NR1CNR1AR1B, —NHC(O)NR1AR1B, —N(O)m1, —NR1AR1B, —C(O)R1C, —C(O)—OR1C, —C(O) NR1AR1B, —OR1D, —NR1ASO2R1D, —NR1AC(O)R1C, —NR1AC(O)OR1C, —NR1AOR1C, —SF5, —N3, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl; two adjacent R1 substituents on adjacent carbons may optionally be joined to form a substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl or two R1 substituents bonded to the same carbon atom may optionally be joined to form a substituted or unsubstituted alkyl or substituted or unsubstituted heterocycloalkyl.
z1 is an integer from 0 to 9.
R2 is independently oxo, halogen, —CX23, —CHX22, —CH2X2, —OCX23, —OCH2X2, —OCHX22, —CN, —SOn2R2D, —SOv2NR2AR2B, —NR2CNR2AR2B, —ONR2AR2B, —NHC(O)NR2CNR2AR2B, —NHC(O)NR2AR2B, —N(O)m2, —NR2AR2B, —C(O)R2C, —C(O)—OR2C, —C(O) NR2AR2B, —OR2D, —NR2ASO2R2D, —NR2AC(O)R2C, —NR2AC(O)OR2C, —NR2AOR2C, —SF5, —N3, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl; two adjacent R2 substituents on adjacent carbons may optionally be joined to form a substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted phenyl, or substituted or unsubstituted heteroaryl.
z2 is an integer from 0 to 6.
L3 is a bond, —S(O)2—, —NR3—, —NH—, —O—, —S—, —C(O)—, —C(O)NR3—, —NR3C(O)—, —N(R3)CH2—, —NR3C(O)NH —, —NHC(O)NR3—, —C(O)O—, —OC(O)—, substituted or unsubstituted alkylene, or substituted or unsubstituted heteroalkylene.
L4 is a bond, —NH—, —NR4—, or substituted or unsubstituted alkylene.
L6 is —N(R6)—L3— or —C(O)NH—.
W5 is CH or N.
z6 is 1 or 2.
R3, R4, and R6 are independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CO(C1—C6 alkyl), —CONH2, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2 Cl, —OCH2Br, —OCH2I, —OCH2F, unsubstituted alkyl, unsubstituted heteroalkyl, unsubstituted cycloalkyl, or unsubstituted heterocycloalkyl.
R7, R8, R9, and R10 are independently hydrogen or unsubstituted C1-C10 alkyl;
Ring B is aryl, or heteroaryl.
R5 is an electrophilic moiety.
R1A, R1B, R1C, R1D, R2A, R2B, R2C, and R2D are independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHC12, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl; R1A and R1B substituents bonded to the same nitrogen atom may optionally be joined to form a substituted or unsubstituted heterocycloalkyl or substituted or unsubstituted heteroaryl; R2A and R2B substituents bonded to the same nitrogen atom may optionally be joined to form a substituted or unsubstituted heterocycloalkyl or substituted or unsubstituted heteroaryl.
X1 and X2 are independently —F, —Cl, —Br, or —I.
n1 and n2 are independently an integer from 0 to 4.
m1, m2, v1, and v2 are independently 1 or 2.
In an aspect is provided a pharmaceutical composition including a compound as described herein and a pharmaceutically acceptable excipient.
In an aspect is provided a method of inhibiting human Caspase 6 protein activity, the method including: contacting the human Caspase 6 protein with a compound as described herein.
In an aspect is provided a method of treating a neurodegenerative disease, the method including administering to a subject in need thereof an effective amount of a compound as disclosed herein.
In an aspect is provided a method of treating a memory loss, the method including administering to a subject in need thereof an effective amount of a compound as disclosed herein.
In an aspect is provided a method of treating axonal degradation, the method including administering to a subject in need thereof an effective amount of a compound as disclosed herein.
In an aspect is provided a method of treating an inflammatory disease, the method including administering to a subject in need thereof an effective amount of a compound as disclosed herein.
In an aspect is provided a method of treating neuroinflammation, the method including administering to a subject in need thereof an effective amount of a compound as disclosed herein.
In an aspect is provided a method of treating liver disease, the method including administering to a subject in need thereof an effective amount of a compound as disclosed herein.
In an aspect is provided a method of treating nonalcoholic steatohepatitis or nonalcoholic fatty liver disease, the method including administering to a subject in need thereof an effective amount of a compound as disclosed herein.
In an aspect is provided a method of treating a fibrotic disease, the method including administering to a subject in need thereof an effective amount of a compound as disclosed herein.
The abbreviations used herein have their conventional meaning within the chemical and biological arts. The chemical structures and formulae set forth herein are constructed according to the standard rules of chemical valency known in the chemical arts.
Where substituent groups are specified by their conventional chemical formulae, written from left to right, they equally encompass the chemically identical substituents that would result from writing the structure from right to left, e.g., —CH2O— is equivalent to —OCH2—.
The term “alkyl,” by itself or as part of another substituent, means, unless otherwise stated, a straight (i.e., unbranched) or branched carbon chain (or carbon), or combination thereof, which may be fully saturated, mono- or polyunsaturated and can include mono-, di- and multivalent radicals. The alkyl may include a designated number of carbons (e.g., C1-C10 means one to ten carbons). Alkyl is an uncyclized chain. Examples of saturated hydrocarbon radicals include, but are not limited to, groups such as methyl, ethyl, n-propyl, isopropyl, n-butyl, t-butyl, isobutyl, sec-butyl, methyl, homologs and isomers of, for example, n-pentyl, n-hexyl, n-heptyl, n-octyl, and the like. An unsaturated alkyl group is one having one or more double bonds or triple bonds. Examples of unsaturated alkyl groups include, but are not limited to, vinyl, 2-propenyl, crotyl, 2-isopentenyl, 2-(butadienyl), 2,4-pentadienyl, 3-(1,4-pentadienyl), ethynyl, 1-and 3-propynyl, 3-butynyl, and the higher homologs and isomers. An alkoxy is an alkyl attached to the remainder of the molecule via an oxygen linker (—O—). An alkyl moiety may be an alkenyl moiety. An alkyl moiety may be an alkynyl moiety. An alkyl moiety may be fully saturated. An alkenyl may include more than one double bond and/or one or more triple bonds in addition to the one or more double bonds. An alkynyl may include more than one triple bond and/or one or more double bonds in addition to the one or more triple bonds. In embodiments, the alkyl is fully saturated. In embodiments, the alkyl is monounsaturated. In embodiments, the alkyl is polyunsaturated.
The term “alkylene,” by itself or as part of another substituent, means, unless otherwise stated, a divalent radical derived from an alkyl, as exemplified, but not limited by, —CH2CH2CH2CH2—. Typically, an alkyl (or alkylene) group will have from 1 to 24 carbon atoms, with those groups having 10 or fewer carbon atoms being preferred herein. A “lower alkyl” or “lower alkylene” is a shorter chain alkyl or alkylene group, generally having eight or fewer carbon atoms. The term “alkenylene,” by itself or as part of another substituent, means, unless otherwise stated, a divalent radical derived from an alkene. In embodiments, the alkylene is fully saturated. In embodiments, the alkylene is monounsaturated. In embodiments, the alkylene is polyunsaturated. In embodiments, an alkenylene includes one or more double bonds. In embodiments, an alkynylene includes one or more triple bonds.
The term “heteroalkyl,” by itself or in combination with another term, means, unless otherwise stated, a stable straight or branched chain, or combinations thereof, including at least one carbon atom and at least one heteroatom (e.g., O, N, P, Si, and S), and wherein the nitrogen and sulfur atoms may optionally be oxidized, and the nitrogen heteroatom may optionally be quaternized. The heteroatom(s) (e.g., O, N, S, Si, or P) may be placed at any interior position of the heteroalkyl group or at the position at which the alkyl group is attached to the remainder of the molecule. Heteroalkyl is an uncyclized chain. Examples include, but are not limited to: —CH2—CH2—O—CH3, —CH2—CH2—NH—CH3, —CH2—CH2—N(CH3)—CH3, —CH2—S—CH2—CH3, —CH2—S—CH2, —S(O)—CH3, —CH2—CH2—S(O)2—CH3, —CH═CH—O—CH3, —Si(CH3)3, —CH2—CH═N—OCH3, —CH═CH—N(CH3)—CH3, —O—CH3, —O—CH—2—CH3, and —CN. Up to two or three heteroatoms may be consecutive, such as, for example, —CH2—NH—OCH3 and —CH2—O—Si(CH3)3. A heteroalkyl moiety may include one heteroatom (e.g., O, N, S, Si, or P). A heteroalkyl moiety may include two optionally different heteroatoms (e.g., O, N, S, Si, or P). A heteroalkyl moiety may include three optionally different heteroatoms (e.g., O, N, S, Si, or P). A heteroalkyl moiety may include four optionally different heteroatoms (e.g., O, N, S, Si, or P). A heteroalkyl moiety may include five optionally different heteroatoms (e.g., O, N, S, Si, or P). A heteroalkyl moiety may include up to 8 optionally different heteroatoms (e.g., O, N, S, Si, or P). The term “heteroalkenyl,” by itself or in combination with another term, means, unless otherwise stated, a heteroalkyl including at least one double bond. A heteroalkenyl may optionally include more than one double bond and/or one or more triple bonds in additional to the one or more double bonds. The term “heteroalkynyl,” by itself or in combination with another term, means, unless otherwise stated, a heteroalkyl including at least one triple bond. A heteroalkynyl may optionally include more than one triple bond and/or one or more double bonds in additional to the one or more triple bonds. In embodiments, the heteroalkyl is fully saturated. In embodiments, the heteroalkyl is monounsaturated. In embodiments, the heteroalkyl is polyunsaturated.
Similarly, the term “heteroalkylene,” by itself or as part of another substituent, means, unless otherwise stated, a divalent radical derived from heteroalkyl, as exemplified, but not limited by, —CH2—CH2—S—CH2—CH2— and —CH2—S—CH2—CH2—NH—CH2—. For heteroalkylene groups, heteroatoms can also occupy either or both of the chain termini (e.g., alkyleneoxy, alkylenedioxy, alkyleneamino, alkylenediamino, and the like). Still further, for alkylene and heteroalkylene linking groups, no orientation of the linking group is implied by the direction in which the formula of the linking group is written. For example, the formula —C(O)2R’— represents both —C(O)2R’— and —R’C(O)2—. As described above, heteroalkyl groups, as used herein, include those groups that are attached to the remainder of the molecule through a heteroatom, such as —C(O)R’, —C(O)NR’, -NR’R”, -OR’, -SR’, and/or —SO2R’. Where “heteroalkyl” is recited, followed by recitations of specific heteroalkyl groups, such as -NR’R” or the like, it will be understood that the terms heteroalkyl and -NR′R″ are not redundant or mutually exclusive. Rather, the specific heteroalkyl groups are recited to add clarity. Thus, the term “heteroalkyl” should not be interpreted herein as excluding specific heteroalkyl groups, such as -NR’R” or the like. The term “heteroalkenylene,” by itself or as part of another substituent, means, unless otherwise stated, a divalent radical derived from a heteroalkene. The term “heteroalkynylene” by itself or as part of another substituent, means, unless otherwise stated, a divalent radical derived from a heteroalkyne. In embodiments, the heteroalkylene is fully saturated. In embodiments, the heteroalkylene is monounsaturated. In embodiments, the heteroalkylene is polyunsaturated. In embodiments, a heteroalkenylene includes one or more double bonds. In embodiments, a heteroalkynylene includes one or more triple bonds.
The terms “cycloalkyl” and “heterocycloalkyl,” by themselves or in combination with other terms, mean, unless otherwise stated, cyclic versions of “alkyl” and “heteroalkyl,” respectively. Cycloalkyl and heterocycloalkyl are not aromatic. Additionally, for heterocycloalkyl, a heteroatom can occupy the position at which the heterocycle is attached to the remainder of the molecule. Examples of cycloalkyl include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, 1-cyclohexenyl, 3-cyclohexenyl, cycloheptyl, and the like. Examples of heterocycloalkyl include, but are not limited to, 1-(1,2,5,6-tetrahydropyridyl), 1-piperidinyl, 2-piperidinyl, 3-piperidinyl, 4-morpholinyl, 3-morpholinyl, tetrahydrofuran-2-yl, tetrahydrofuran-3-yl, tetrahydrothien-2-yl, tetrahydrothien-3-yl, 1-piperazinyl, 2-piperazinyl, and the like. A “cycloalkylene” and a “heterocycloalkylene,” alone or as part of another substituent, means a divalent radical derived from a cycloalkyl and heterocycloalkyl, respectively. In embodiments, the cycloalkyl is fully saturated. In embodiments, the cycloalkyl is monounsaturated. In embodiments, the cycloalkyl is polyunsaturated. In embodiments, the heterocycloalkyl is fully saturated. In embodiments, the heterocycloalkyl is monounsaturated. In embodiments, the heterocycloalkyl is polyunsaturated.
In embodiments, the term “cycloalkyl” means a monocyclic, bicyclic, or a multicyclic cycloalkyl ring system. In embodiments, monocyclic ring systems are cyclic hydrocarbon groups containing from 3 to 8 carbon atoms, where such groups can be saturated or unsaturated, but not aromatic. In embodiments, cycloalkyl groups are fully saturated. In embodiments, a bicyclic or multicyclic cycloalkyl ring system refers to multiple rings fused together wherein at least one of the fused rings is a cycloalkyl ring and wherein the multiple rings are attached to the parent molecular moiety through any carbon atom contained within a cycloalkyl ring of the multiple rings. Examples of monocyclic cycloalkyls include cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, cyclohexenyl, cycloheptyl, and cyclooctyl. Bicyclic cycloalkyl ring systems are bridged monocyclic rings or fused bicyclic rings. In embodiments, bridged monocyclic rings contain a monocyclic cycloalkyl ring where two non adjacent carbon atoms of the monocyclic ring are linked by an alkylene bridge of between one and three additional carbon atoms (i.e., a bridging group of the form (CH2)w , where w is 1, 2, or 3). Representative examples of bicyclic ring systems include, but are not limited to, bicyclo[3.1.1]heptane, bicyclo[2.2.1]heptane, bicyclo[2.2.2]octane, bicyclo[3.2.2]nonane, bicyclo[3.3.1]nonane, and bicyclo[4.2.1]nonane. In embodiments, fused bicyclic cycloalkyl ring systems contain a monocyclic cycloalkyl ring fused to either a phenyl, a monocyclic cycloalkyl, a monocyclic cycloalkenyl, a monocyclic heterocyclyl, or a monocyclic heteroaryl. In embodiments, the bridged or fused bicyclic cycloalkyl is attached to the parent molecular moiety through any carbon atom contained within the monocyclic cycloalkyl ring. In embodiments, cycloalkyl groups are optionally substituted with one or two groups which are independently oxo or thia. In embodiments, the fused bicyclic cycloalkyl is a 5 or 6 membered monocyclic cycloalkyl ring fused to either a phenyl ring, a 5 or 6 membered monocyclic cycloalkyl, a 5 or 6 membered monocyclic cycloalkenyl, a 5 or 6 membered monocyclic heterocyclyl, or a 5 or 6 membered monocyclic heteroaryl, wherein the fused bicyclic cycloalkyl is optionally substituted by one or two groups which are independently oxo or thia. In embodiments, multicyclic cycloalkyl ring systems are a monocyclic cycloalkyl ring (base ring) fused to either (i) one ring system selected from the group consisting of a bicyclic aryl, a bicyclic heteroaryl, a bicyclic cycloalkyl, a bicyclic cycloalkenyl, and a bicyclic heterocyclyl; or (ii) two other ring systems independently selected from the group consisting of a phenyl, a bicyclic aryl, a monocyclic or bicyclic heteroaryl, a monocyclic or bicyclic cycloalkyl, a monocyclic or bicyclic cycloalkenyl, and a monocyclic or bicyclic heterocyclyl. In embodiments, the multicyclic cycloalkyl is attached to the parent molecular moiety through any carbon atom contained within the base ring. In embodiments, multicyclic cycloalkyl ring systems are a monocyclic cycloalkyl ring (base ring) fused to either (i) one ring system selected from the group consisting of a bicyclic aryl, a bicyclic heteroaryl, a bicyclic cycloalkyl, a bicyclic cycloalkenyl, and a bicyclic heterocyclyl; or (ii) two other ring systems independently selected from the group consisting of a phenyl, a monocyclic heteroaryl, a monocyclic cycloalkyl, a monocyclic cycloalkenyl, and a monocyclic heterocyclyl. Examples of multicyclic cycloalkyl groups include, but are not limited to tetradecahydrophenanthrenyl, perhydrophenothiazin-1-yl, and perhydrophenoxazin-1-yl.
In embodiments, a cycloalkyl is a cycloalkenyl. The term “cycloalkenyl” is used in accordance with its plain ordinary meaning. In embodiments, a cycloalkenyl is a monocyclic, bicyclic, or a multicyclic cycloalkenyl ring system. In embodiments, a bicyclic or multicyclic cycloalkenyl ring system refers to multiple rings fused together wherein at least one of the fused rings is a cycloalkenyl ring and wherein the multiple rings are attached to the parent molecular moiety through any carbon atom contained within a cycloalkenyl ring of the multiple rings. In embodiments, monocyclic cycloalkenyl ring systems are cyclic hydrocarbon groups containing from 3 to 8 carbon atoms, where such groups are unsaturated (i.e., containing at least one annular carbon carbon double bond), but not aromatic. Examples of monocyclic cycloalkenyl ring systems include cyclopentenyl and cyclohexenyl. In embodiments, bicyclic cycloalkenyl rings are bridged monocyclic rings or a fused bicyclic rings. In embodiments, bridged monocyclic rings contain a monocyclic cycloalkenyl ring where two non adjacent carbon atoms of the monocyclic ring are linked by an alkylene bridge of between one and three additional carbon atoms (i.e., a bridging group of the form (CH2)w, where w is 1, 2, or 3). Representative examples of bicyclic cycloalkenyls include, but are not limited to, norbornenyl and bicyclo[2.2.2]oct 2 enyl. In embodiments, fused bicyclic cycloalkenyl ring systems contain a monocyclic cycloalkenyl ring fused to either a phenyl, a monocyclic cycloalkyl, a monocyclic cycloalkenyl, a monocyclic heterocyclyl, or a monocyclic heteroaryl. In embodiments, the bridged or fused bicyclic cycloalkenyl is attached to the parent molecular moiety through any carbon atom contained within the monocyclic cycloalkenyl ring. In embodiments, cycloalkenyl groups are optionally substituted with one or two groups which are independently oxo or thia. In embodiments, multicyclic cycloalkenyl rings contain a monocyclic cycloalkenyl ring (base ring) fused to either (i) one ring system selected from the group consisting of a bicyclic aryl, a bicyclic heteroaryl, a bicyclic cycloalkyl, a bicyclic cycloalkenyl, and a bicyclic heterocyclyl; or (ii) two ring systems independently selected from the group consisting of a phenyl, a bicyclic aryl, a monocyclic or bicyclic heteroaryl, a monocyclic or bicyclic cycloalkyl, a monocyclic or bicyclic cycloalkenyl, and a monocyclic or bicyclic heterocyclyl. In embodiments, the multicyclic cycloalkenyl is attached to the parent molecular moiety through any carbon atom contained within the base ring. In embodiments, multicyclic cycloalkenyl rings contain a monocyclic cycloalkenyl ring (base ring) fused to either (i) one ring system selected from the group consisting of a bicyclic aryl, a bicyclic heteroaryl, a bicyclic cycloalkyl, a bicyclic cycloalkenyl, and a bicyclic heterocyclyl; or (ii) two ring systems independently selected from the group consisting of a phenyl, a monocyclic heteroaryl, a monocyclic cycloalkyl, a monocyclic cycloalkenyl, and a monocyclic heterocyclyl.
In embodiments, the term “heterocycloalkyl” means a monocyclic, bicyclic, or a multicyclic heterocycloalkyl ring system. In embodiments, heterocycloalkyl groups are fully saturated. In embodiments, a bicyclic or multicyclic heterocycloalkyl ring system refers to multiple rings fused together wherein at least one of the fused rings is a heterocycloalkyl ring and wherein the multiple rings are attached to the parent molecular moiety through any atom contained within a heterocycloalkyl ring of the multiple rings. In embodiments, a heterocycloalkyl is a heterocyclyl. The term “heterocyclyl” as used herein, means a monocyclic, bicyclic, or multicyclic heterocycle. The heterocyclyl monocyclic heterocycle is a 3, 4, 5, 6 or 7 membered ring containing at least one heteroatom independently selected from the group consisting of O, N, and S where the ring is saturated or unsaturated, but not aromatic. The 3 or 4 membered ring contains 1 heteroatom selected from the group consisting of O, N and S. The 5 membered ring can contain zero or one double bond and one, two or three heteroatoms selected from the group consisting of O, N and S. The 6 or 7 membered ring contains zero, one or two double bonds and one, two or three heteroatoms selected from the group consisting of O, N and S. The heterocyclyl monocyclic heterocycle is connected to the parent molecular moiety through any carbon atom or any nitrogen atom contained within the heterocyclyl monocyclic heterocycle. Representative examples of heterocyclyl monocyclic heterocycles include, but are not limited to, azetidinyl, azepanyl, aziridinyl, diazepanyl, 1,3-dioxanyl, 1,3-dioxolanyl, 1,3-dithiolanyl, 1,3-dithianyl, imidazolinyl, imidazolidinyl, isothiazolinyl, isothiazolidinyl, isoxazolinyl, isoxazolidinyl, morpholinyl, oxadiazolinyl, oxadiazolidinyl, oxazolinyl, oxazolidinyl, piperazinyl, piperidinyl, pyranyl, pyrazolinyl, pyrazolidinyl, pyrrolinyl, pyrrolidinyl, tetrahydrofuranyl, tetrahydrothienyl, thiadiazolinyl, thiadiazolidinyl, thiazolinyl, thiazolidinyl, thiomorpholinyl, 1,1-dioxidothiomorpholinyl (thiomorpholine sulfone), thiopyranyl, and trithianyl. The heterocyclyl bicyclic heterocycle is a monocyclic heterocycle fused to either a phenyl, a monocyclic cycloalkyl, a monocyclic cycloalkenyl, a monocyclic heterocycle, or a monocyclic heteroaryl. The heterocyclyl bicyclic heterocycle is connected to the parent molecular moiety through any carbon atom or any nitrogen atom contained within the monocyclic heterocycle portion of the bicyclic ring system. Representative examples of bicyclic heterocyclyls include, but are not limited to, 2,3-dihydrobenzofuran-2-yl, 2,3-dihydrobenzofuran-3-yl, indolin-1-yl, indolin-2-yl, indolin-3-yl, 2,3-dihydrobenzothien-2-yl, decahydroquinolinyl, decahydroisoquinolinyl, octahydro-1H-indolyl, and octahydrobenzofuranyl. In embodiments, heterocyclyl groups are optionally substituted with one or two groups which are independently oxo or thia. In certain embodiments, the bicyclic heterocyclyl is a 5 or 6 membered monocyclic heterocyclyl ring fused to a phenyl ring, a 5 or 6 membered monocyclic cycloalkyl, a 5 or 6 membered monocyclic cycloalkenyl, a 5 or 6 membered monocyclic heterocyclyl, or a 5 or 6 membered monocyclic heteroaryl, wherein the bicyclic heterocyclyl is optionally substituted by one or two groups which are independently oxo or thia. Multicyclic heterocyclyl ring systems are a monocyclic heterocyclyl ring (base ring) fused to either (i) one ring system selected from the group consisting of a bicyclic aryl, a bicyclic heteroaryl, a bicyclic cycloalkyl, a bicyclic cycloalkenyl, and a bicyclic heterocyclyl; or (ii) two other ring systems independently selected from the group consisting of a phenyl, a bicyclic aryl, a monocyclic or bicyclic heteroaryl, a monocyclic or bicyclic cycloalkyl, a monocyclic or bicyclic cycloalkenyl, and a monocyclic or bicyclic heterocyclyl. The multicyclic heterocyclyl is attached to the parent molecular moiety through any carbon atom or nitrogen atom contained within the base ring. In embodiments, multicyclic heterocyclyl ring systems are a monocyclic heterocyclyl ring (base ring) fused to either (i) one ring system selected from the group consisting of a bicyclic aryl, a bicyclic heteroaryl, a bicyclic cycloalkyl, a bicyclic cycloalkenyl, and a bicyclic heterocyclyl; or (ii) two other ring systems independently selected from the group consisting of a phenyl, a monocyclic heteroaryl, a monocyclic cycloalkyl, a monocyclic cycloalkenyl, and a monocyclic heterocyclyl. Examples of multicyclic heterocyclyl groups include, but are not limited to 10H-phenothiazin-10-yl, 9,10-dihydroacridin-9-yl, 9,10-dihydroacridin-10-yl, 10H-phenoxazin-10-yl, 10,11-dihydro-5H-dibenzo[b,f]azepin-5-yl, 1,2,3,4-tetrahydropyrido[4,3-g]isoquinolin-2-yl, 12H-benzo[b]phenoxazin-12-yl, and dodecahydro- 1H-carbazol-9-yl.
The terms “halo” or “halogen,” by themselves or as part of another substituent, mean, unless otherwise stated, a fluorine, chlorine, bromine, or iodine atom. Additionally, terms such as “haloalkyl” are meant to include monohaloalkyl and polyhaloalkyl. For example, the term “halo(C1-C4)alkyl” includes, but is not limited to, fluoromethyl, difluoromethyl, trifluoromethyl, 2,2,2-trifluoroethyl, 4-chlorobutyl, 3-bromopropyl, and the like.
The term “acyl” means, unless otherwise stated, —C(O)R where R is a substituted or unsubstituted alkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl.
The term “aryl” means, unless otherwise stated, a polyunsaturated, aromatic, hydrocarbon substituent, which can be a single ring or multiple rings (preferably from 1 to 3 rings) that are fused together (i.e., a fused ring aryl) or linked covalently. A fused ring aryl refers to multiple rings fused together wherein at least one of the fused rings is an aryl ring. In embodiments, a fused ring aryl refers to multiple rings fused together wherein at least one of the fused rings is an aryl ring and wherein the multiple rings are attached to the parent molecular moiety through any carbon atom contained within an aryl ring of the multiple rings. The term “heteroaryl” refers to aryl groups (or rings) that contain at least one heteroatom such as N, O, or S, wherein the nitrogen and sulfur atoms are optionally oxidized, and the nitrogen atom(s) are optionally quaternized. Thus, the term “heteroaryl” includes fused ring heteroaryl groups (i.e., multiple rings fused together wherein at least one of the fused rings is a heteroaromatic ring). In embodiments, the term “heteroaryl” includes fused ring heteroaryl groups (i.e., multiple rings fused together wherein at least one of the fused rings is a heteroaromatic ring and wherein the multiple rings are attached to the parent molecular moiety through any atom contained within a heteroaromatic ring of the multiple rings). A 5,6-fused ring heteroarylene refers to two rings fused together, wherein one ring has 5 members and the other ring has 6 members, and wherein at least one ring is a heteroaryl ring. Likewise, a 6,6-fused ring heteroarylene refers to two rings fused together, wherein one ring has 6 members and the other ring has 6 members, and wherein at least one ring is a heteroaryl ring. And a 6,5-fused ring heteroarylene refers to two rings fused together, wherein one ring has 6 members and the other ring has 5 members, and wherein at least one ring is a heteroaryl ring. A heteroaryl group can be attached to the remainder of the molecule through a carbon or heteroatom. Non-limiting examples of aryl and heteroaryl groups include phenyl, naphthyl, pyrrolyl, pyrazolyl, pyridazinyl, triazinyl, pyrimidinyl, imidazolyl, pyrazinyl, purinyl, oxazolyl, isoxazolyl, thiazolyl, furyl, thienyl, pyridyl, pyrimidyl, benzothiazolyl, benzoxazoyl, benzimidazolyl, benzofuran, isobenzofuranyl, indolyl, isoindolyl, benzothiophenyl, isoquinolyl, quinoxalinyl, quinolyl, 1-naphthyl, 2-naphthyl, 4-biphenyl, 1-pyrrolyl, 2-pyrrolyl, 3-pyrrolyl, 3-pyrazolyl, 2-imidazolyl, 4-imidazolyl, pyrazinyl, 2-oxazolyl, 4-oxazolyl, 2-phenyl-4-oxazolyl, 5-oxazolyl, 3-isoxazolyl, 4-isoxazolyl, 5-isoxazolyl, 2-thiazolyl, 4-thiazolyl, 5-thiazolyl, 2-furyl, 3-furyl, 2-thienyl, 3-thienyl, 2-pyridyl, 3-pyridyl, 4-pyridyl, 2-pyrimidyl, 4-pyrimidyl, 5-benzothiazolyl, purinyl, 2-benzimidazolyl, 5-indolyl, 1-isoquinolyl, 5-isoquinolyl, 2-quinoxalinyl, 5-quinoxalinyl, 3-quinolyl, and 6-quinolyl. Substituents for each of the above noted aryl and heteroaryl ring systems are selected from the group of acceptable substituents described below. An “arylene” and a “heteroarylene,” alone or as part of another substituent, mean a divalent radical derived from an aryl and heteroaryl, respectively. A heteroaryl group substituent may be —O— bonded to a ring heteroatom nitrogen.
A fused ring heterocyloalkyl-aryl is an aryl fused to a heterocycloalkyl. A fused ring heterocycloalkyl-heteroaryl is a heteroaryl fused to a heterocycloalkyl. A fused ring heterocycloalkyl-cycloalkyl is a heterocycloalkyl fused to a cycloalkyl. A fused ring heterocycloalkyl-heterocycloalkyl is a heterocycloalkyl fused to another heterocycloalkyl. Fused ring heterocycloalkyl-aryl, fused ring heterocycloalkyl-heteroaryl, fused ring heterocycloalkyl-cycloalkyl, or fused ring heterocycloalkyl-heterocycloalkyl may each independently be unsubstituted or substituted with one or more of the substitutents described herein.
Spirocyclic rings are two or more rings wherein adjacent rings are attached through a single atom. The individual rings within spirocyclic rings may be identical or different. Individual rings in spirocyclic rings may be substituted or unsubstituted and may have different substituents from other individual rings within a set of spirocyclic rings. Possible substituents for individual rings within spirocyclic rings are the possible substituents for the same ring when not part of spirocyclic rings (e.g. substituents for cycloalkyl or heterocycloalkyl rings). Spirocylic rings may be substituted or unsubstituted cycloalkyl, substituted or unsubstituted cycloalkylene, substituted or unsubstituted heterocycloalkyl or substituted or unsubstituted heterocycloalkylene and individual rings within a spirocyclic ring group may be any of the immediately previous list, including having all rings of one type (e.g. all rings being substituted heterocycloalkylene wherein each ring may be the same or different substituted heterocycloalkylene). When referring to a spirocyclic ring system, heterocyclic spirocyclic rings means a spirocyclic rings wherein at least one ring is a heterocyclic ring and wherein each ring may be a different ring. When referring to a spirocyclic ring system, substituted spirocyclic rings means that at least one ring is substituted and each substituent may optionally be different.
The symbol “〰” denotes the point of attachment of a chemical moiety to the remainder of a molecule or chemical formula.
The term “oxo,” as used herein, means an oxygen that is double bonded to a carbon atom.
The term “alkylsulfonyl,” as used herein, means a moiety having the formula —S(O2)—R’, where R’ is a substituted or unsubstituted alkyl group as defined above. R’ may have a specified number of carbons (e.g., “C1-C4 alkylsulfonyl”).
The term “alkylarylene” as an arylene moiety covalently bonded to an alkylene moiety (also referred to herein as an alkylene linker). In embodiments, the alkylarylene group has the formula:
An alkylarylene moiety may be substituted (e.g. with a substituent group) on the alkylene moiety or the arylene linker (e.g. at carbons 2, 3, 4, or 6) with halogen, oxo, —N3, —CF3, —CCl3, —CBr3, —CI3, —CN, —CHO, —OH, —NH2, —COOH, —CONH2, —NO2, —SH, —SO2CH3 —SO3H, —OSO3H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, substituted or unsubstituted C1-C5 alkyl or substituted or unsubstituted 2 to 5 membered heteroalkyl). In embodiments, the alkylarylene is unsubstituted.
Each of the above terms (e.g., “alkyl,” “heteroalkyl,” “cycloalkyl,” “heterocycloalkyl,” “aryl,” and “heteroaryl”) includes both substituted and unsubstituted forms of the indicated radical. Preferred substituents for each type of radical are provided below.
Substituents for the alkyl and heteroalkyl radicals (including those groups often referred to as alkylene, alkenyl, heteroalkylene, heteroalkenyl, alkynyl, cycloalkyl, heterocycloalkyl, cycloalkenyl, and heterocycloalkenyl) can be one or more of a variety of groups selected from, but not limited to, —OR’, ═O, ═NR’, ═N—OR’, —NR’R”, —SR’, -halogen, —SiR’R”R’”, —OC(O)R’, —C(O)R’, —CO2R’, —CONR’R”, —OC(O)NR’R”, —NR”C(O)R’, —NR’—C(O)NR”R’”, —NR”C(O)2R’, —NR—C(NR’R”R’═”)═NR””, —NR—C(NR’R”)═NR’”, —S(O)R’, —S(O)2R’, —S(O)2NR’R”, —NRSO2R’, —NR’NR”R’”, —ONR’R”, —NR’C(O)NR”NR’”R””, —CN, —NO2, —NR’SO2R”, —NR’C(O)R”, —NR’C(O)—OR”, —NR’OR”, in a number ranging from zero to (2m’+1), where m’ is the total number of carbon atoms in such radical. R, R’, R”, R’”, and R”” each preferably independently refer to hydrogen, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl (e.g., aryl substituted with 1-3 halogens), substituted or unsubstituted heteroaryl, substituted or unsubstituted alkyl, alkoxy, or thioalkoxy groups, or arylalkyl groups. When a compound described herein includes more than one R group, for example, each of the R groups is independently selected as are each R’, R”, R’”, and R”” group when more than one of these groups is present. When R’ and R” are attached to the same nitrogen atom, they can be combined with the nitrogen atom to form a 4-, 5-, 6-, or 7-membered ring. For example, —NR’R” includes, but is not limited to, 1-pyrrolidinyl and 4-morpholinyl. From the above discussion of substituents, one of skill in the art will understand that the term “alkyl” is meant to include groups including carbon atoms bound to groups other than hydrogen groups, such as haloalkyl (e.g., —CF3 and —CH2CF3) and acyl (e.g., —C(O)CH3, —C(O)CF3, —C(O)CH2OCH3, and the like).
Similar to the substituents described for the alkyl radical, substituents for the aryl and heteroaryl groups are varied and are selected from, for example: —OR’, —NR’R”, —SR’, -halogen, —SiR’R”R’”, —OC(O)R’, —C(O)R’, —CO2R’, —CONR’R”, —OC(O)NR’R”, —NR”C(O)R’, —NR’—C(O)NR”R’”, —N”C(O)2R’, —NR—C(NR’R”R’”)═NR””, —NR—C(NR’R”)═NR’”, —S(O)R’, —S(O)2R’, —S(O)2NR’R” , —NRSO2R’, —NR’NR”R’”, —ONR’R”, —NR’C(O)NRNR’”R””, —CN, —NO2, —R’, —N3, —CH(Ph)2, fluoro(C1-C4)alkoxy, and fluoro(C1-C4)alkyl, —NR‘SO2R”, —NR’C(O)R”, —NR’C(O)—OR”, —NR’OR”, in a number ranging from zero to the total number of open valences on the aromatic ring system; and where R’, R”, R’”, and R”” are preferably independently selected from hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, and substituted or unsubstituted heteroaryl. When a compound described herein includes more than one R group, for example, each of the R groups is independently selected as are each R’, R”, R’”, and R”” groups when more than one of these groups is present.
Substituents for rings (e.g. cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkylene, heterocycloalkylene, arylene, or heteroarylene) may be depicted as substituents on the ring rather than on a specific atom of a ring (commonly referred to as a floating substituent). In such a case, the substituent may be attached to any of the ring atoms (obeying the rules of chemical valency) and in the case of fused rings or spirocyclic rings, a substituent depicted as associated with one member of the fused rings or spirocyclic rings (a floating substituent on a single ring), may be a substituent on any of the fused rings or spirocyclic rings (a floating substituent on multiple rings). When a substituent is attached to a ring, but not a specific atom (a floating substituent), and a subscript for the substituent is an integer greater than one, the multiple substituents may be on the same atom, same ring, different atoms, different fused rings, different spirocyclic rings, and each substituent may optionally be different. Where a point of attachment of a ring to the remainder of a molecule is not limited to a single atom (a floating substituent), the attachment point may be any atom of the ring and in the case of a fused ring or spirocyclic ring, any atom of any of the fused rings or spirocyclic rings while obeying the rules of chemical valency. Where a ring, fused rings, or spirocyclic rings contain one or more ring heteroatoms and the ring, fused rings, or spirocyclic rings are shown with one more floating substituents (including, but not limited to, points of attachment to the remainder of the molecule), the floating substituents may be bonded to the heteroatoms. Where the ring heteroatoms are shown bound to one or more hydrogens (e.g. a ring nitrogen with two bonds to ring atoms and a third bond to a hydrogen) in the structure or formula with the floating substituent, when the heteroatom is bonded to the floating substituent, the substituent will be understood to replace the hydrogen, while obeying the rules of chemical valency.
Two or more substituents on adjacent carbons may optionally be joined to form aryl, heteroaryl, cycloalkyl, or heterocycloalkyl groups. Such so-called ring-forming substituents are typically, though not necessarily, found attached to a cyclic base structure. In one embodiment, the ring-forming substituents are attached to adjacent members of the base structure. For example, two ring-forming substituents attached to adjacent members of a cyclic base structure create a fused ring structure. In another embodiment, the ring-forming substituents are attached to a single member of the base structure. For example, two ring-forming substituents attached to a single member of a cyclic base structure create a spirocyclic structure. In yet another embodiment, the ring-forming substituents are attached to non-adjacent members of the base structure.
Two of the substituents on adjacent atoms of the aryl or heteroaryl ring may optionally form a ring of the formula —T—C(O)—(CRR’)q—U—, wherein T and U are independently —NR—, —O—, —CRR’—, or a single bond, and q is an integer of from 0 to 3. Alternatively, two of the substituents on adjacent atoms of the aryl or heteroaryl ring may optionally be replaced with a substituent of the formula —A—(CH2)r—B—, wherein A and B are independently —CRR’—, —O—, —NR—, —S—, —S(O)—, —S(O)2—, —S(O)2NR’—, or a single bond, and r is an integer of from 1 to 4. One of the single bonds of the new ring so formed may optionally be replaced with a double bond. Alternatively, two of the substituents on adjacent atoms of the aryl or heteroaryl ring may optionally be replaced with a substituent of the formula —(CRR′)s—X’— (C”R”R’”)d—, where s and d are independently integers of from 0 to 3, and X’ is —O—, —NR’—, —S—, —S(O)—, —S(O)2—, or —S(O)2NR’—. The substituents R, R’, R”, and R’” are preferably independently selected from hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, and substituted or unsubstituted heteroaryl.
As used herein, the terms “heteroatom” or “ring heteroatom” are meant to include oxygen (O), nitrogen (N), sulfur (S), phosphorus (P), and silicon (Si).
A “substituent group,” as used herein, means a group selected from the following moieties:
A “size-limited substituent” or “ size-limited substituent group,” as used herein, means a group selected from all of the substituents described above for a “substituent group,” wherein each substituted or unsubstituted alkyl is a substituted or unsubstituted C1-C20 alkyl, each substituted or unsubstituted heteroalkyl is a substituted or unsubstituted 2 to 20 membered heteroalkyl, each substituted or unsubstituted cycloalkyl is a substituted or unsubstituted C3-C8 cycloalkyl, each substituted or unsubstituted heterocycloalkyl is a substituted or unsubstituted 3 to 8 membered heterocycloalkyl, each substituted or unsubstituted aryl is a substituted or unsubstituted C6-C10 aryl, and each substituted or unsubstituted heteroaryl is a substituted or unsubstituted 5 to 10 membered heteroaryl.
A “lower substituent” or “ lower substituent group,” as used herein, means a group selected from all of the substituents described above for a “substituent group,” wherein each substituted or unsubstituted alkyl is a substituted or unsubstituted C1-C8 alkyl, each substituted or unsubstituted heteroalkyl is a substituted or unsubstituted 2 to 8 membered heteroalkyl, each substituted or unsubstituted cycloalkyl is a substituted or unsubstituted C3-C7 cycloalkyl, each substituted or unsubstituted heterocycloalkyl is a substituted or unsubstituted 3 to 7 membered heterocycloalkyl, each substituted or unsubstituted aryl is a substituted or unsubstituted C6-C10 aryl, and each substituted or unsubstituted heteroaryl is a substituted or unsubstituted 5 to 9 membered heteroaryl.
In some embodiments, each substituted group described in the compounds herein is substituted with at least one substituent group. More specifically, in some embodiments, each substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, substituted heteroaryl, substituted alkylene, substituted heteroalkylene, substituted cycloalkylene, substituted heterocycloalkylene, substituted arylene, and/or substituted heteroarylene described in the compounds herein are substituted with at least one substituent group. In other embodiments, at least one or all of these groups are substituted with at least one size-limited substituent group. In other embodiments, at least one or all of these groups are substituted with at least one lower substituent group.
In other embodiments of the compounds herein, each substituted or unsubstituted alkyl may be a substituted or unsubstituted C1-C20 alkyl, each substituted or unsubstituted heteroalkyl is a substituted or unsubstituted 2 to 20 membered heteroalkyl, each substituted or unsubstituted cycloalkyl is a substituted or unsubstituted C3-C8 cycloalkyl, each substituted or unsubstituted heterocycloalkyl is a substituted or unsubstituted 3 to 8 membered heterocycloalkyl, each substituted or unsubstituted aryl is a substituted or unsubstituted C6-C10 aryl, and/or each substituted or unsubstituted heteroaryl is a substituted or unsubstituted 5 to 10 membered heteroaryl. In some embodiments of the compounds herein, each substituted or unsubstituted alkylene is a substituted or unsubstituted C1-C20 alkylene, each substituted or unsubstituted heteroalkylene is a substituted or unsubstituted 2 to 20 membered heteroalkylene, each substituted or unsubstituted cycloalkylene is a substituted or unsubstituted C3-C8 cycloalkylene, each substituted or unsubstituted heterocycloalkylene is a substituted or unsubstituted 3 to 8 membered heterocycloalkylene, each substituted or unsubstituted arylene is a substituted or unsubstituted C6-C10 arylene, and/or each substituted or unsubstituted heteroarylene is a substituted or unsubstituted 5 to 10 membered heteroarylene.
In some embodiments, each substituted or unsubstituted alkyl is a substituted or unsubstituted C1-C8 alkyl, each substituted or unsubstituted heteroalkyl is a substituted or unsubstituted 2 to 8 membered heteroalkyl, each substituted or unsubstituted cycloalkyl is a substituted or unsubstituted C3-C7 cycloalkyl, each substituted or unsubstituted heterocycloalkyl is a substituted or unsubstituted 3 to 7 membered heterocycloalkyl, each substituted or unsubstituted aryl is a substituted or unsubstituted C6-C10 aryl, and/or each substituted or unsubstituted heteroaryl is a substituted or unsubstituted 5 to 9 membered heteroaryl. In some embodiments, each substituted or unsubstituted alkylene is a substituted or unsubstituted C1-C8 alkylene, each substituted or unsubstituted heteroalkylene is a substituted or unsubstituted 2 to 8 membered heteroalkylene, each substituted or unsubstituted cycloalkylene is a substituted or unsubstituted C3-C7 cycloalkylene, each substituted or unsubstituted heterocycloalkylene is a substituted or unsubstituted 3 to 7 membered heterocycloalkylene, each substituted or unsubstituted arylene is a substituted or unsubstituted C6-C10 arylene, and/or each substituted or unsubstituted heteroarylene is a substituted or unsubstituted 5 to 9 membered heteroarylene. In some embodiments, the compound is a chemical species set forth in the Examples section, figures, or tables below.
In embodiments, a substituted or unsubstituted moiety (e.g., substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted alkylene, substituted or unsubstituted heteroalkylene, substituted or unsubstituted cycloalkylene, substituted or unsubstituted heterocycloalkylene, substituted or unsubstituted arylene, and/or substituted or unsubstituted heteroarylene) is unsubstituted (e.g., is an unsubstituted alkyl, unsubstituted heteroalkyl, unsubstituted cycloalkyl, unsubstituted heterocycloalkyl, unsubstituted aryl, unsubstituted heteroaryl, unsubstituted alkylene, unsubstituted heteroalkylene, unsubstituted cycloalkylene, unsubstituted heterocycloalkylene, unsubstituted arylene, and/or unsubstituted heteroarylene, respectively). In embodiments, a substituted or unsubstituted moiety (e.g., substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted alkylene, substituted or unsubstituted heteroalkylene, substituted or unsubstituted cycloalkylene, substituted or unsubstituted heterocycloalkylene, substituted or unsubstituted arylene, and/or substituted or unsubstituted heteroarylene) is substituted (e.g., is a substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, substituted heteroaryl, substituted alkylene, substituted heteroalkylene, substituted cycloalkylene, substituted heterocycloalkylene, substituted arylene, and/or substituted heteroarylene, respectively).
In embodiments, a substituted moiety (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, substituted heteroaryl, substituted alkylene, substituted heteroalkylene, substituted cycloalkylene, substituted heterocycloalkylene, substituted arylene, and/or substituted heteroarylene) is substituted with at least one substituent group, wherein if the substituted moiety is substituted with a plurality of substituent groups, each substituent group may optionally be different. In embodiments, if the substituted moiety is substituted with a plurality of substituent groups, each substituent group is different.
In embodiments, a substituted moiety (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, substituted heteroaryl, substituted alkylene, substituted heteroalkylene, substituted cycloalkylene, substituted heterocycloalkylene, substituted arylene, and/or substituted heteroarylene) is substituted with at least one size-limited substituent group, wherein if the substituted moiety is substituted with a plurality of size-limited substituent groups, each size-limited substituent group may optionally be different. In embodiments, if the substituted moiety is substituted with a plurality of size-limited substituent groups, each size-limited substituent group is different.
In embodiments, a substituted moiety (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, substituted heteroaryl, substituted alkylene, substituted heteroalkylene, substituted cycloalkylene, substituted heterocycloalkylene, substituted arylene, and/or substituted heteroarylene) is substituted with at least one lower substituent group, wherein if the substituted moiety is substituted with a plurality of lower substituent groups, each lower substituent group may optionally be different. In embodiments, if the substituted moiety is substituted with a plurality of lower substituent groups, each lower substituent group is different.
In embodiments, a substituted moiety (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, substituted heteroaryl, substituted alkylene, substituted heteroalkylene, substituted cycloalkylene, substituted heterocycloalkylene, substituted arylene, and/or substituted heteroarylene) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted moiety is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different. In embodiments, if the substituted moiety is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group is different.
Certain compounds of the present disclosure possess asymmetric carbon atoms (optical or chiral centers) or double bonds; the enantiomers, racemates, diastereomers, tautomers, geometric isomers, stereoisometric forms that may be defined, in terms of absolute stereochemistry, as (R)-or (S)- or, as (D)- or (L)- for amino acids, and individual isomers are encompassed within the scope of the present disclosure. The compounds of the present disclosure do not include those that are known in art to be too unstable to synthesize and/or isolate. The present disclosure is meant to include compounds in racemic and optically pure forms. Optically active (R)- and (S)-, or (D)- and (L)-isomers may be prepared using chiral synthons or chiral reagents, or resolved using conventional techniques. When the compounds described herein contain olefinic bonds or other centers of geometric asymmetry, and unless specified otherwise, it is intended that the compounds include both E and Z geometric isomers.
As used herein, the term “isomers” refers to compounds having the same number and kind of atoms, and hence the same molecular weight, but differing in respect to the structural arrangement or configuration of the atoms.
The term “tautomer,” as used herein, refers to one of two or more structural isomers which exist in equilibrium and which are readily converted from one isomeric form to another.
It will be apparent to one skilled in the art that certain compounds of this disclosure may exist in tautomeric forms, all such tautomeric forms of the compounds being within the scope of the disclosure.
Unless otherwise stated, structures depicted herein are also meant to include all stereochemical forms of the structure; i.e., the R and S configurations for each asymmetric center. Therefore, single stereochemical isomers as well as enantiomeric and diastereomeric mixtures of the present compounds are within the scope of the disclosure.
Unless otherwise stated, structures depicted herein are also meant to include compounds which differ only in the presence of one or more isotopically enriched atoms. For example, compounds having the present structures except for the replacement of a hydrogen by a deuterium or tritium, or the replacement of a carbon by 13C- or 14C-enriched carbon are within the scope of this disclosure.
The compounds of the present disclosure may also contain unnatural proportions of atomic isotopes at one or more of the atoms that constitute such compounds. For example, the compounds may be radiolabeled with radioactive isotopes, such as for example tritium (3H), iodine-125 (125I), or carbon-14 (14C). All isotopic variations of the compounds of the present disclosure, whether radioactive or not, are encompassed within the scope of the present disclosure.
It should be noted that throughout the application that alternatives are written in Markush groups, for example, each amino acid position that contains more than one possible amino acid. It is specifically contemplated that each member of the Markush group should be considered separately, thereby comprising another embodiment, and the Markush group is not to be read as a single unit.
As used herein, the term “bioconjugate” and “bioconjugate linker” refers to the resulting association between atoms or molecules of “bioconjugate reactive groups” or “bioconjugate reactive moieties”. The association can be direct or indirect. For example, a conjugate between a first bioconjugate reactive group (e.g., —NH2, —C(O)OH, —N—hydroxysuccinimide, or -maleimide) and a second bioconjugate reactive group (e.g., sulfhydryl, sulfur-containing amino acid, amine, amine sidechain containing amino acid, or carboxylate) provided herein can be direct, e.g., by covalent bond or linker (e.g. a first linker of second linker), or indirect, e.g., by non-covalent bond (e.g. electrostatic interactions (e.g. ionic bond, hydrogen bond, halogen bond), van der Waals interactions (e.g. dipole-dipole, dipole-induced dipole, London dispersion), ring stacking (pi effects), hydrophobic interactions and the like). In embodiments, bioconjugates or bioconjugate linkers are formed using bioconjugate chemistry (i.e. the association of two bioconjugate reactive groups) including, but are not limited to nucleophilic substitutions (e.g., reactions of amines and alcohols with acyl halides, active esters), electrophilic substitutions (e.g., enamine reactions) and additions to carbon-carbon and carbon-heteroatom multiple bonds (e.g., Michael reaction, Diels-Alder addition). These and other useful reactions are discussed in, for example, March, ADVANCED ORGANIC CHEMISTRY, 3rd Ed., John Wiley & Sons, New York, 1985; Hermanson, BIOCONJUGATE TECHNIQUES, Academic Press, San Diego, 1996; and Feeney et al., MODIFICATION OF PROTEINS; Advances in Chemistry Series, Vol. 198, American Chemical Society, Washington, D.C., 1982. In embodiments, the first bioconjugate reactive group (e.g., maleimide moiety) is covalently attached to the second bioconjugate reactive group (e.g. a sulfhydryl). In embodiments, the first bioconjugate reactive group (e.g., haloacetyl moiety) is covalently attached to the second bioconjugate reactive group (e.g. a sulfhydryl). In embodiments, the first bioconjugate reactive group (e.g., pyridyl moiety) is covalently attached to the second bioconjugate reactive group (e.g. a sulfhydryl). In embodiments, the first bioconjugate reactive group (e.g., -N-hydroxysuccinimide moiety) is covalently attached to the second bioconjugate reactive group (e.g. an amine). In embodiments, the first bioconjugate reactive group (e.g., maleimide moiety) is covalently attached to the second bioconjugate reactive group (e.g. a sulfhydryl). In embodiments, the first bioconjugate reactive group (e.g., -sulfo-N-hydroxysuccinimide moiety) is covalently attached to the second bioconjugate reactive group (e.g. an amine).
Useful bioconjugate reactive moieties used for bioconjugate chemistries herein include, for example:
The bioconjugate reactive groups can be chosen such that they do not participate in, or interfere with, the chemical stability of the conjugate described herein. Alternatively, a reactive functional group can be protected from participating in the crosslinking reaction by the presence of a protecting group. In embodiments, the bioconjugate comprises a molecular entity derived from the reaction of an unsaturated bond, such as a maleimide, and a sulfhydryl group.
“Analog,” or “analogue” is used in accordance with its plain ordinary meaning within Chemistry and Biology and refers to a chemical compound that is structurally similar to another compound (i.e., a so-called “reference” compound) but differs in composition, e.g., in the replacement of one atom by an atom of a different element, or in the presence of a particular functional group, or the replacement of one functional group by another functional group, or the absolute stereochemistry of one or more chiral centers of the reference compound. Accordingly, an analog is a compound that is similar or comparable in function and appearance but not in structure or origin to a reference compound.
The terms “a” or “an,” as used in herein means one or more. In addition, the phrase “substituted with a[n],” as used herein, means the specified group may be substituted with one or more of any or all of the named substituents. For example, where a group, such as an alkyl or heteroaryl group, is “substituted with an unsubstituted C1-C20 alkyl, or unsubstituted 2 to 20 membered heteroalkyl,” the group may contain one or more unsubstituted C1-C20 alkyls, and/or one or more unsubstituted 2 to 20 membered heteroalkyls.
Moreover, where a moiety is substituted with an R substituent, the group may be referred to as “R-substituted.” Where a moiety is R-substituted, the moiety is substituted with at least one R substituent and each R substituent is optionally different. Where a particular R group is present in the description of a chemical genus (such as Formula (I)), a Roman alphabetic symbol may be used to distinguish each appearance of that particular R group. For example, where multiple R13 substituents are present, each R13 substituent may be distinguished as R13.1, R13.2, R 13.3, R 13.4, etc., wherein each of R 13.1, R13.2, R 13.3, R 13.4, etc. is defined within the scope of the definition of R13 and optionally differently.
A “detectable agent” or “detectable moiety” is a composition, substance, element, or compound; or moiety thereof; detectable by appropriate means such as spectroscopic, photochemical, biochemical, immunochemical, chemical, magnetic resonance imaging, or other physical means. For example, useful detectable agents include 18F, 32P, 33P, 45Ti, 47Sc, 52Fe, 59Fe, 62Cu, 64Cu, 67Cu, 67Ga, 68Ga, 77As, 86Y, 90Y. 89Sr, 89Zr, 94Tc, 94Tc, 99mTc, 99Mo, 105Pd, 105Rh, 111Ag, 111In, 123I, 124I, 125I, 131I, 142Pr, 143Pr, 149Pm, 153Sm, 154-1581Gd, 161Tb, 166Dy, 166Ho, 169Er, 175Lu, 177Lu, 186Re, 188Re, 189Re, 194Ir, 198Au, 199Au, 211At, 211Pb, 212Bi, 212Pb, 213Bi, 223Ra, 225Ac, Cr, V, Mn, Fe, Co, Ni, Cu, La, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, 32P, fluorophore (e.g. fluorescent dyes), electron-dense reagents, enzymes (e.g., as commonly used in an ELISA), biotin, digoxigenin, paramagnetic molecules, paramagnetic nanoparticles, ultrasmall superparamagnetic iron oxide (“USPIO”) nanoparticles, USPIO nanoparticle aggregates, superparamagnetic iron oxide (“SPIO”) nanoparticles, SPIO nanoparticle aggregates, monochrystalline iron oxide nanoparticles, monochrystalline iron oxide, nanoparticle contrast agents, liposomes or other delivery vehicles containing Gadolinium chelate (“Gd-chelate”) molecules, Gadolinium, radioisotopes, radionuclides (e.g. carbon-11, nitrogen-13, oxygen-15, fluorine-18, rubidium-82), fluorodeoxyglucose (e.g. fluorine-18 labeled), any gamma ray emitting radionuclides, positron-emitting radionuclide, radiolabeled glucose, radiolabeled water, radiolabeled ammonia, biocolloids, microbubbles (e.g. including microbubble shells including albumin, galactose, lipid, and/or polymers; microbubble gas core including air, heavy gas(es), perfluorcarbon, nitrogen, octafluoropropane, perflexane lipid microsphere, perflutren, etc.), iodinated contrast agents (e.g. iohexol, iodixanol, ioversol, iopamidol, ioxilan, iopromide, diatrizoate, metrizoate, ioxaglate), barium sulfate, thorium dioxide, gold, gold nanoparticles, gold nanoparticle aggregates, fluorophores, two-photon fluorophores, or haptens and proteins or other entities which can be made detectable, e.g., by incorporating a radiolabel into a peptide or antibody specifically reactive with a target peptide. A detectable moiety is a monovalent detectable agent or a detectable agent capable of forming a bond with another composition.
Radioactive substances (e.g., radioisotopes) that may be used as imaging and/or labeling agents in accordance with the embodiments of the disclosure include, but are not limited to, 18F, 32P, 33P, 45Ti, 47Sc, 52Fe, 59Fe, 62Cu, 64Cu, 67Cu, 67Ga, 68Ga, 77As, 86Y, 90Y. 89Sr, 89Zr, 94Tc, 94Tc, 99mTc, 99Mo, 105Pd, 105Rh, 111Ag, 111In, 123I, 124I, 125I, 131I, 142Pr, 143Pr, 149Pm, 153Sm, 154-1581Gd, 161Tb, 166Dy, 166Ho, 169Er, 175Lu, 177Lu, 186Re, 188Re, 189Re, 194Ir, 198Au, 199Au, 211At, 211Pb, 212Bi, 212Pb, 213Bi, 223Ra and 225Ac. Paramagnetic ions that may be used as additional imaging agents in accordance with the embodiments of the disclosure include, but are not limited to, ions of transition and lanthanide metals (e.g. metals having atomic numbers of 21-29, 42, 43, 44, or 57-71). These metals include ions of Cr, V, Mn, Fe, Co, Ni, Cu, La, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb and Lu.
Descriptions of compounds of the present disclosure are limited by principles of chemical bonding known to those skilled in the art. Accordingly, where a group may be substituted by one or more of a number of substituents, such substitutions are selected so as to comply with principles of chemical bonding and to give compounds which are not inherently unstable and/or would be known to one of ordinary skill in the art as likely to be unstable under ambient conditions, such as aqueous, neutral, and several known physiological conditions. For example, a heterocycloalkyl or heteroaryl is attached to the remainder of the molecule via a ring heteroatom in compliance with principles of chemical bonding known to those skilled in the art thereby avoiding inherently unstable compounds.
A person of ordinary skill in the art will understand when a variable (e.g., moiety or linker) of a compound or of a compound genus (e.g., a genus described herein) is described by a name or formula of a standalone compound with all valencies filled, the unfilled valence(s) of the variable will be dictated by the context in which the variable is used. For example, when a variable of a compound as described herein is connected (e.g., bonded) to the remainder of the compound through a single bond, that variable is understood to represent a monovalent form (i.e., capable of forming a single bond due to an unfilled valence) of a standalone compound (e.g., if the variable is named “methane” in an embodiment but the variable is known to be attached by a single bond to the remainder of the compound, a person of ordinary skill in the art would understand that the variable is actually a monovalent form of methane, i.e., methyl or -CH3). Likewise, for a linker variable (e.g., L1, L2, or L3 as described herein), a person of ordinary skill in the art will understand that the variable is the divalent form of a standalone compound (e.g., if the variable is assigned to “PEG” or “polyethylene glycol” in an embodiment but the variable is connected by two separate bonds to the remainder of the compound, a person of ordinary skill in the art would understand that the variable is a divalent (i.e., capable of forming two bonds through two unfilled valences) form of PEG instead of the standalone compound PEG).
The term “exogenous” refers to a molecule or substance (e.g., a compound, nucleic acid or protein) that originates from outside a given cell or organism. For example, an “exogenous promoter” as referred to herein is a promoter that does not originate from the plant it is expressed by. Conversely, the term “endogenous” or “endogenous promoter” refers to a molecule or substance that is native to, or originates within, a given cell or organism.
A charged moiety refers to a functional group possessing an abundance of electron density (i.e. electronegative) or is deficient in electron density (i.e. electropositive). Non-limiting examples of a charged moiety includes carboxylic acid, alcohol, phosphate, aldehyde, and sulfonamide. In embodiments, a charged moiety is capable of forming hydrogen bonds.
The terms “bind” and “bound” as used herein is used in accordance with its plain and ordinary meaning and refers to the association between atoms or molecules. The association can be direct or indirect. For example, bound atoms or molecules may be direct, e.g., by covalent bond or linker (e.g. a first linker or second linker), or indirect, e.g., by non-covalent bond (e.g. electrostatic interactions (e.g. ionic bond, hydrogen bond, halogen bond), van der Waals interactions (e.g. dipole-dipole, dipole-induced dipole, London dispersion), ring stacking (pi effects), hydrophobic interactions and the like).
The term “capable of binding” as used herein refers to a moiety (e.g. a compound as described herein) that is able to measurably bind to a target (e.g., a NF-κB, a Toll-like receptor protein). In embodiments, where a moiety is capable of binding a target, the moiety is capable of binding with a Kd of less than about 10 µM, 5 µM, 1 µM, 500 nM, 250 nM, 100 nM, 75 nM, 50 nM, 25 nM, 15 nM, 10 nM, 5 nM, 1 nM, or about 0.1 nM.
As used herein, the term “salt” refers to acid or base salts of the compounds used in the methods of the present invention. Illustrative examples of acceptable salts are mineral acid (hydrochloric acid, hydrobromic acid, phosphoric acid, and the like) salts, organic acid (acetic acid, propionic acid, glutamic acid, citric acid and the like) salts, quaternary ammonium (methyl iodide, ethyl iodide, and the like) salts.
The term “pharmaceutically acceptable salts” is meant to include salts of the active compounds that are prepared with relatively nontoxic acids or bases, depending on the particular substituents found on the compounds described herein. When compounds of the present disclosure contain relatively acidic functionalities, base addition salts can be obtained by contacting the neutral form of such compounds with a sufficient amount of the desired base, either neat or in a suitable inert solvent. Examples of pharmaceutically acceptable base addition salts include sodium, potassium, calcium, ammonium, organic amino, or magnesium salt, or a similar salt. When compounds of the present disclosure contain relatively basic functionalities, acid addition salts can be obtained by contacting the neutral form of such compounds with a sufficient amount of the desired acid, either neat or in a suitable inert solvent. Examples of pharmaceutically acceptable acid addition salts include those derived from inorganic acids like hydrochloric, hydrobromic, nitric, carbonic, monohydrogencarbonic, phosphoric, monohydrogenphosphoric, dihydrogenphosphoric, sulfuric, monohydrogensulfuric, hydriodic, or phosphorous acids and the like, as well as the salts derived from relatively nontoxic organic acids like acetic, propionic, isobutyric, maleic, malonic, benzoic, succinic, suberic, fumaric, lactic, mandelic, phthalic, benzenesulfonic, p-tolylsulfonic, citric, tartaric, oxalic, methanesulfonic, and the like. Also included are salts of amino acids such as arginate and the like, and salts of organic acids like glucuronic or galactunoric acids and the like (see, for example, Berge et al., “Pharmaceutical Salts”, Journal of Pharmaceutical Science, 1977, 66, 1-19). Certain specific compounds of the present disclosure contain both basic and acidic functionalities that allow the compounds to be converted into either base or acid addition salts.
Thus, the compounds of the present disclosure may exist as salts, such as with pharmaceutically acceptable acids. The present disclosure includes such salts. Non-limiting examples of such salts include hydrochlorides, hydrobromides, phosphates, sulfates, methanesulfonates, nitrates, maleates, acetates, citrates, fumarates, proprionates, tartrates (e.g., (+)-tartrates, (-)-tartrates, or mixtures thereof including racemic mixtures), succinates, benzoates, and salts with amino acids such as glutamic acid, and quaternary ammonium salts (e.g. methyl iodide, ethyl iodide, and the like). These salts may be prepared by methods known to those skilled in the art.
The neutral forms of the compounds are preferably regenerated by contacting the salt with a base or acid and isolating the parent compound in the conventional manner. The parent form of the compound may differ from the various salt forms in certain physical properties, such as solubility in polar solvents.
In addition to salt forms, the present disclosure provides compounds, which are in a prodrug form. Prodrugs of the compounds described herein are those compounds that readily undergo chemical changes under physiological conditions to provide the compounds of the present disclosure. Prodrugs of the compounds described herein may be converted in vivo after administration. Additionally, prodrugs can be converted to the compounds of the present disclosure by chemical or biochemical methods in an ex vivo environment, such as, for example, when contacted with a suitable enzyme or chemical reagent.
Certain compounds of the present disclosure can exist in unsolvated forms as well as solvated forms, including hydrated forms. In general, the solvated forms are equivalent to unsolvated forms and are encompassed within the scope of the present disclosure. Certain compounds of the present disclosure may exist in multiple crystalline or amorphous forms. In general, all physical forms are equivalent for the uses contemplated by the present disclosure and are intended to be within the scope of the present disclosure.
“Pharmaceutically acceptable excipient” and “pharmaceutically acceptable carrier” refer to a substance that aids the administration of an active agent to and absorption by a subject and can be included in the compositions of the present disclosure without causing a significant adverse toxicological effect on the patient. Non-limiting examples of pharmaceutically acceptable excipients include water, NaCl, normal saline solutions, lactated Ringer’s, normal sucrose, normal glucose, binders, fillers, disintegrants, lubricants, coatings, sweeteners, flavors, salt solutions (such as Ringer’s solution), alcohols, oils, gelatins, carbohydrates such as lactose, amylose or starch, fatty acid esters, hydroxymethycellulose, polyvinyl pyrrolidine, and colors, and the like. Such preparations can be sterilized and, if desired, mixed with auxiliary agents such as lubricants, preservatives, stabilizers, wetting agents, emulsifiers, salts for influencing osmotic pressure, buffers, coloring, and/or aromatic substances and the like that do not deleteriously react with the compounds of the disclosure. One of skill in the art will recognize that other pharmaceutical excipients are useful in the present disclosure.
The term “preparation” is intended to include the formulation of the active compound with encapsulating material as a carrier providing a capsule in which the active component with or without other carriers, is surrounded by a carrier, which is thus in association with it. Similarly, cachets and lozenges are included. Tablets, powders, capsules, pills, cachets, and lozenges can be used as solid dosage forms suitable for oral administration.
As used herein, the term “about” means a range of values including the specified value, which a person of ordinary skill in the art would consider reasonably similar to the specified value. In embodiments, about means within a standard deviation using measurements generally acceptable in the art. In embodiments, about means a range extending to +/- 10% of the specified value. In embodiments, about includes the specified value.
A “synergistic amount” as used herein refers to the sum of a first amount (e.g., an amount of a Caspase 6 inhibitor) and a second amount (e.g., a therapeutic agent) that results in a synergistic effect (i.e. an effect greater than an additive effect). Therefore, the terms “synergy”, “synergism”, “synergistic”, “combined synergistic amount”, and “synergistic therapeutic effect” which are used herein interchangeably, refer to a measured effect of the Caspase 6 inhibitor in combination with a second agent (e.g., an anticancer agent) where the measured effect is greater than the sum of the individual effects of the Caspase 6 inhibitor provided herein and the second agent (e.g., anticancer agent) administered alone as a single agent.
In embodiments, a synergistic amount may be about 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1.0, 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2.0, 2.1, 2.2, 2.3, 2.4, 2.5, 2.6, 2.7, 2.8, 2.9, 3.0, 3.1, 3.2, 3.3, 3.4, 3.5, 3.6, 3.7, 3.8, 3.9, 4.0, 4.1, 4.2, 4.3, 4.4, 4.5, 4.6, 4.7, 4.8, 4.9, 5.0, 5.1, 5.2, 5.3, 5.4, 5.5, 5.6, 5.7, 5.8, 5.9, 6.0, 6.1, 6.2, 6.3, 6.4, 6.5, 6.6, 6.7, 6.8, 6.9, 7.0, 7.1, 7.2, 7.3, 7.4, 7.5, 7.6, 7.7, 7.8, 7.9, 8.0, 8.1, 8.2, 8.3, 8.4, 8.5, 8.6, 8.7, 8.8, 8.9, 9.0, 9.1, 9.2, 9.3, 9.4, 9.5, 9.6, 9.7, 9.8, 9.9, 10.0, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, or 99% of the amount of the Caspase 6 inhibitor provided herein when used separately from the therapeutic agent. In embodiments, a synergistic amount may be about 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1.0, 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2.0, 2.1, 2.2, 2.3, 2.4, 2.5, 2.6, 2.7, 2.8, 2.9, 3.0, 3.1, 3.2, 3.3, 3.4, 3.5, 3.6, 3.7, 3.8, 3.9, 4.0, 4.1, 4.2, 4.3, 4.4, 4.5, 4.6, 4.7, 4.8, 4.9, 5.0, 5.1, 5.2, 5.3, 5.4, 5.5, 5.6, 5.7, 5.8, 5.9, 6.0, 6.1, 6.2, 6.3, 6.4, 6.5, 6.6, 6.7, 6.8, 6.9, 7.0, 7.1, 7.2, 7.3, 7.4, 7.5, 7.6, 7.7, 7.8, 7.9, 8.0, 8.1, 8.2, 8.3, 8.4, 8.5, 8.6, 8.7, 8.8, 8.9, 9.0, 9.1, 9.2, 9.3, 9.4, 9.5, 9.6, 9.7, 9.8, 9.9, 10.0, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, or 99% of the amount of the therapeutic agent when used separately from the Caspase 6 inhibitor provided herein.
The term “EC50” or “half maximal effective concentration” as used herein refers to the concentration of a molecule (e.g., small molecule, antibody, chimeric antigen receptor or bispecific antibody) capable of inducing a response which is halfway between the baseline response and the maximum response after a specified exposure time. In embodiments, the EC50 is the concentration of a molecule (e.g., small molecule, antibody, chimeric antigen receptor or bispecific antibody) that produces 50% of the maximal possible effect of that molecule.
The term “IC50” or “half maximal inhibitory concentration” as used herein refers to the concentration of an inhibitory molecule (e.g., small molecule, antibody, chimeric antigen receptor or bispecific antibody) that is required to inhibit a given biologal process or biological component by 50%.
The term “small molecule” is used in accordance with its well understood meaning and refers to a low molecular weight organic compound that may regulate a biological process. In embodiments, the small molecule is a compound that weighs less than 1000 daltons. In embodiments, the small molecule is a compound that weighs less than 900 daltons. In embodiments, the small molecule weighs less than 800 daltons. In embodiments, the small molecule weighs less than 700 daltons. In embodiments, the small molecule weighs less than 600 daltons. In embodiments, the small molecule weighs less than 500 daltons. In embodiments, the small molecule weighs less than 450 daltons. In embodiments, the small molecule weighs less than 400 daltons.
“Contacting” is used in accordance with its plain ordinary meaning and refers to the process of allowing at least two distinct species (e.g. chemical compounds including biomolecules or cells) to become sufficiently proximal to react, interact or physically touch. It should be appreciated; however, the resulting reaction product can be produced directly from a reaction between the added reagents or from an intermediate from one or more of the added reagents that can be produced in the reaction mixture.
The term “contacting” may include allowing two species to react, interact, or physically touch, wherein the two species may be a compound as described herein and a protein or enzyme. In some embodiments contacting includes allowing a compound described herein to interact with a protein or enzyme that is involved in a signaling pathway.
As defined herein, the term “activation”, “activate”, “activating”, “activator” and the like in reference to a protein-inhibitor interaction means positively affecting (e.g. increasing) the activity or function of the protein relative to the activity or function of the protein in the absence of the activator. In embodiments activation means positively affecting (e.g. increasing) the concentration or levels of the protein relative to the concentration or level of the protein in the absence of the activator. The terms may reference activation, or activating, sensitizing, or up-regulating signal transduction or enzymatic activity or the amount of a protein decreased in a disease. Thus, activation may include, at least in part, partially or totally increasing stimulation, increasing or enabling activation, or activating, sensitizing, or up-regulating signal transduction or enzymatic activity or the amount of a protein associated with a disease (e.g., a protein which is decreased in a disease relative to a non-diseased control). Activation may include, at least in part, partially or totally increasing stimulation, increasing or enabling activation, or activating, sensitizing, or up-regulating signal transduction or enzymatic activity or the amount of a protein
The terms “agonist,” “activator,” “upregulator,” etc. refer to a substance capable of detectably increasing the expression or activity of a given gene or protein. The agonist can increase expression or activity 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90% or more in comparison to a control in the absence of the agonist. In certain instances, expression or activity is 1.5-fold, 2-fold, 3-fold, 4-fold, 5-fold, 10-fold or higher than the expression or activity in the absence of the agonist.
As defined herein, the term “inhibition”, “inhibit”, “inhibiting” and the like in reference to a protein-inhibitor interaction means negatively affecting (e.g. decreasing) the activity or function of the protein relative to the activity or function of the protein in the absence of the inhibitor. In embodiments inhibition means negatively affecting (e.g. decreasing) the concentration or levels of the protein relative to the concentration or level of the protein in the absence of the inhibitor. In embodiments inhibition refers to reduction of a disease or symptoms of disease. In embodiments, inhibition refers to a reduction in the activity of a particular protein target. Thus, inhibition includes, at least in part, partially or totally blocking stimulation, decreasing, preventing, or delaying activation, or inactivating, desensitizing, or down-regulating signal transduction or enzymatic activity or the amount of a protein. In embodiments, inhibition refers to a reduction of activity of a target protein resulting from a direct interaction (e.g. an inhibitor binds to the target protein). In embodiments, inhibition refers to a reduction of activity of a target protein from an indirect interaction (e.g. an inhibitor binds to a protein that activates the target protein, thereby preventing target protein activation).
A “Caspase 6 inhibitor” refers to a compound (e.g. a compound described herein) that reduces the activity of Caspase 6 when compared to a control, such as absence of the compound or a compound with known inactivity.
The terms “inhibitor,” “repressor” or “antagonist” or “downregulator” interchangeably refer to a substance capable of detectably decreasing the expression or activity of a given gene or protein. The antagonist can decrease expression or activity 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90% or more in comparison to a control in the absence of the antagonist. In certain instances, expression or activity is 1.5-fold, 2-fold, 3-fold, 4-fold, 5-fold, 10-fold or lower than the expression or activity in the absence of the antagonist.
The term “Caspase 6” or “Caspase-6” refers to a protein (including homologs, isoforms, and functional fragments thereof) that is a member of the cysteine-aspartic acid protease (caspase) family. Caspase 6 cleaves substrates (e.g., HTT in Huntington’s, APP in Alzheimer’s disease, tau in Alzheimer’s disease), which may result in protein aggregation of the fragments. In embodiments, caspase 6 cleaves substrates that lead to inflammation (e.g., neuroinflammation), and to cell death. In embodiments, cell death leads to cirrhosis and fibrosis (e.g., in liver or other organs). In embodiments, Caspase 6 is involved in axonal degradation. The term includes any recombinant or naturally-occurring form of Caspase 6 variants thereof that maintain Caspase 6 activity (e.g., within at least 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, or 100% activity compared to wildtype Caspase 6). In embodiments, Caspase 6 is encoded by the CASP6 gene. In embodiments, Caspase 6 has the amino acid sequence set forth in or corresponding to Entrez 839, UniProt P55212, RefSeq (protein) NP_001217.2, or RefSeq (protein) NP_116787.1. In embodiments, Caspase 6 has the sequence:
The term “Caspase 3” or “Caspase-3” refers to a protein (including homologs, isoforms, and functional fragments thereof) that is a member of the cysteine-aspartic acid protease (caspase) family, and cleaves substrates following aspartic acid residues. The term includes any recombinant or naturally-occurring form of Caspase 3 variants thereof that maintain Caspase 3 activity (e.g., within at least 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, or 100% activity compared to wildtype Caspase 3). In embodiments, Caspase 3 is encoded by the CASP3 gene. In embodiments, Caspase 3 has the amino acid sequence set forth in or corresponding to Entrez 836, UniProt P42574, RefSeq (protein) NP_004337.2, RefSeq (protein) NP_116786.1, RefSeq (protein) NP_001341706, RefSeq (protein) NP_001341707, RefSeq (protein) NP_001341708, or XP_011530603.1. In embodiments, Caspase 3 has the sequence:
The term “Caspase 2” or “Caspase-2” refers to a protein (including homologs, isoforms, and functional fragments thereof) that is a member of the cysteine-aspartic acid protease (caspase) family, and cleaves substrates following aspartic acid residues. The term includes any recombinant or naturally-occurring form of Caspase 2 variants thereof that maintain Caspase 2 activity (e.g., within at least 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, or 100% activity compared to wildtype Caspase 2). In embodiments, Caspase 2 is encoded by the CASP2 gene. In embodiments, Caspase 2 has the amino acid sequence set forth in or corresponding to Entrez 835, UniProt P42575, RefSeq (protein) NP_001215.1, RefSeq (protein) NP_116764.2, or RefSeq (protein) NP_116765.2. In embodiments, Caspase 2 has the sequence:
The term “expression” includes any step involved in the production of the polypeptide including, but not limited to, transcription, post-transcriptional modification, translation, post-translational modification, and secretion. Expression can be detected using conventional techniques for detecting protein (e.g., ELISA, Western blotting, flow cytometry, immunofluorescence, immunohistochemistry, etc.).
The term “modulator” refers to a composition that increases or decreases the level of a target molecule or the function of a target molecule or the physical state of the target of the molecule relative to the absence of the modulator. In some embodiments, a Caspase 6 associated disease modulator is a compound that reduces the severity of one or more symptoms of a disease associated with Caspase 6 (e.g. neurodegenerative disease, liver disease, or cancer). A Caspase 6 modulator is a compound that increases or decreases the activity or function or level of activity or level of function of Caspase 6.
The term “modulate” is used in accordance with its plain ordinary meaning and refers to the act of changing or varying one or more properties. “Modulation” refers to the process of changing or varying one or more properties. For example, as applied to the effects of a modulator on a target protein, to modulate means to change by increasing or decreasing a property or function of the target molecule or the amount of the target molecule.
The term “associated” or “associated with” in the context of a substance or substance activity or function associated with a disease (e.g. a protein associated disease, a cancer associated with Caspase 6 activity, Caspase 6 associated cancer, Caspase 6 associated disease (e.g., neurodegenerative disease, liver disease, cancer, inflammatory disease, autoimmune disease, or infectious disease)) means that the disease (e.g. neurodegenerative disease, liver disease, cancer, inflammatory disease, autoimmune disease, or infectious disease) is caused by (in whole or in part), or a symptom of the disease is caused by (in whole or in part) the substance or substance activity or function. For example, a cancer associated with Caspase 6 activity or function may be a cancer that results (entirely or partially) from aberrant Caspase 6 function (e.g. enzyme activity, protein-protein interaction, signaling pathway) or a cancer wherein a particular symptom of the disease is caused (entirely or partially) by aberrant Caspase 6 activity or function. As used herein, what is described as being associated with a disease, if a causative agent, could be a target for treatment of the disease. For example, a cancer associated with Caspase 6 activity or function or a Caspase 6 associated disease (e.g., neurodegenerative disease, liver disease, cancer, inflammatory disease, autoimmune disease, or infectious disease), may be treated with a Caspase 6 modulator or Caspase 6 inhibitor, in the instance where increased Caspase 6 activity or function (e.g. signaling pathway activity) causes the disease (e.g., neurodegenerative disease, liver disease, cancer, inflammatory disease, autoimmune disease, or infectious disease).
The term “aberrant” as used herein refers to different from normal. When used to describe enzymatic activity or protein function, aberrant refers to activity or function that is greater or less than a normal control or the average of normal non-diseased control samples. Aberrant activity may refer to an amount of activity that results in a disease, wherein returning the aberrant activity to a normal or non-disease-associated amount (e.g. by administering a compound or using a method as described herein), results in reduction of the disease or one or more disease symptoms.
The term “signaling pathway” as used herein refers to a series of interactions between cellular and optionally extra-cellular components (e.g. proteins, nucleic acids, small molecules, ions, lipids) that conveys a change in one component to one or more other components, which in turn may convey a change to additional components, which is optionally propagated to other signaling pathway components. For example, binding of a Caspase 6 with a compound as described herein may reduce the level of a product of the Caspase 6 catalyzed reaction or the level of a downstream derivative of the product or binding may reduce the interactions between the Caspase 6 enzyme or a Caspase 6 reaction product and downstream effectors or signaling pathway components (e.g., epigenetic regulatory proteins MLL and the transcription factor (TF) IIA family of nuclear proteins), resulting in changes in cell growth, proliferation, or survival.
In this disclosure, “comprises,” “comprising,” “containing” and “having” and the like can have the meaning ascribed to them in U.S. Patent law and can mean “includes,” “including,” and the like. “Consisting essentially of or “consists essentially” likewise has the meaning ascribed in U.S. Patent law and the term is open-ended, allowing for the presence of more than that which is recited so long as basic or novel characteristics of that which is recited is not changed by the presence of more than that which is recited, but excludes prior art embodiments.
The terms “disease” or “condition” refer to a state of being or health status of a patient or subject capable of being treated with the compounds or methods provided herein. The disease may be a neurodegenerative disease. The disease may be a liver disease. The disease may be a cancer. The disease may be an autoimmune disease. The disease may be an inflammatory disease. The disease may be an infectious disease. In some further instances, “cancer” refers to human cancers and carcinomas, sarcomas, adenocarcinomas, lymphomas, leukemias, etc., including solid and lymphoid cancers, kidney, breast, lung, bladder, colon, ovarian, prostate, pancreas, stomach, brain, head and neck, skin, uterine, testicular, glioma, esophagus, and liver cancer, including hepatocarcinoma, lymphoma, including B-acute lymphoblastic lymphoma, non-Hodgkin’s lymphomas (e.g., Burkitt’s, Small Cell, and Large Cell lymphomas), Hodgkin’s lymphoma, leukemia (including AML, ALL, and CML), or multiple myeloma.
As used herein, the term “inflammatory disease” refers to a disease or condition characterized by aberrant inflammation (e.g. an increased level of inflammation compared to a control such as a healthy person not suffering from a disease). Examples of inflammatory diseases include autoimmune diseases, arthritis, rheumatoid arthritis, psoriatic arthritis, juvenile idiopathic arthritis, multiple sclerosis, systemic lupus erythematosus (SLE), myasthenia gravis, juvenile onset diabetes, diabetes mellitus type 1, Guillain-Barre syndrome, Hashimoto’s encephalitis, Hashimoto’s thyroiditis, ankylosing spondylitis, psoriasis, Sjogren’s syndrome, vasculitis, glomerulonephritis, auto-immune thyroiditis, Behcet’s disease, Crohn’s disease, ulcerative colitis, bullous pemphigoid, sarcoidosis, ichthyosis, Graves ophthalmopathy, inflammatory bowel disease, Addison’s disease, Vitiligo, asthma, allergic asthma, acne vulgaris, celiac disease, chronic prostatitis, inflammatory bowel disease, pelvic inflammatory disease, reperfusion injury, ischemia reperfusion injury, stroke, sarcoidosis, transplant rejection, interstitial cystitis, atherosclerosis, scleroderma, and atopic dermatitis.
As used herein, the term “cancer” refers to all types of cancer, neoplasm or malignant tumors found in mammals (e.g. humans), including leukemias, lymphomas, carcinomas and sarcomas. Exemplary cancers that may be treated with a compound or method provided herein include brain cancer, glioma, glioblastoma, neuroblastoma, prostate cancer, colorectal cancer, pancreatic cancer, Medulloblastoma, melanoma, cervical cancer, gastric cancer, ovarian cancer, lung cancer, cancer of the head, Hodgkin’s Disease, and Non-Hodgkin’s Lymphomas. Exemplary cancers that may be treated with a compound or method provided herein include cancer of the thyroid, endocrine system, brain, breast, cervix, colon, head & neck, liver, kidney, lung, ovary, pancreas, rectum, stomach, and uterus. Additional examples include, thyroid carcinoma, cholangiocarcinoma, pancreatic adenocarcinoma, skin cutaneous melanoma, colon adenocarcinoma, rectum adenocarcinoma, stomach adenocarcinoma, esophageal carcinoma, head and neck squamous cell carcinoma, breast invasive carcinoma, lung adenocarcinoma, lung squamous cell carcinoma, non-small cell lung carcinoma, mesothelioma, multiple myeloma, neuroblastoma, glioma, glioblastoma multiforme, ovarian cancer, rhabdomyosarcoma, primary thrombocytosis, primary macroglobulinemia, primary brain tumors, malignant pancreatic insulanoma, malignant carcinoid, urinary bladder cancer, premalignant skin lesions, testicular cancer, thyroid cancer, neuroblastoma, esophageal cancer, genitourinary tract cancer, malignant hypercalcemia, endometrial cancer, adrenal cortical cancer, neoplasms of the endocrine or exocrine pancreas, medullary thyroid cancer, medullary thyroid carcinoma, melanoma, colorectal cancer, papillary thyroid cancer, hepatocellular carcinoma, or prostate cancer.
As used herein, the term “autoimmune disease” refers to a disease or condition in which a subject’s immune system has an aberrant immune response against a substance that does not normally elicit an immune response in a healthy subject. Examples of autoimmune diseases that may be treated with a compound, pharmaceutical composition, or method described herein include Acute Disseminated Encephalomyelitis (ADEM), Acute necrotizing hemorrhagic leukoencephalitis, Addison’s disease, Agammaglobulinemia, Alopecia areata, Amyloidosis, Ankylosing spondylitis, Anti-GBM/Anti-TBM nephritis, Antiphospholipid syndrome (APS), Autoimmune angioedema, Autoimmune aplastic anemia, Autoimmune dysautonomia, Autoimmune hepatitis, Autoimmune hyperlipidemia, Autoimmune immunodeficiency, Autoimmune inner ear disease (AIED), Autoimmune myocarditis, Autoimmune oophoritis, Autoimmune pancreatitis, Autoimmune retinopathy, Autoimmune thrombocytopenic purpura (ATP), Autoimmune thyroid disease, Autoimmune urticaria, Axonal or neuronal neuropathies, Balo disease, Behcet’s disease, Bullous pemphigoid, Cardiomyopathy, Castleman disease, Celiac disease, Chagas disease, Chronic fatigue syndrome, Chronic inflammatory demyelinating polyneuropathy (CIDP), Chronic recurrent multifocal ostomyelitis (CRMO), Churg-Strauss syndrome, Cicatricial pemphigoid/benign mucosal pemphigoid, Crohn’s disease, Cogans syndrome, Cold agglutinin disease, Congenital heart block, Coxsackie myocarditis, CREST disease, Essential mixed cryoglobulinemia, Demyelinating neuropathies, Dermatitis herpetiformis, Dermatomyositis, Devic’s disease (neuromyelitis optica), Discoid lupus, Dressler’s syndrome, Endometriosis, Eosinophilic esophagitis, Eosinophilic fasciitis, Erythema nodosum, Experimental allergic encephalomyelitis, Evans syndrome, Fibromyalgia , Fibrosing alveolitis, Giant cell arteritis (temporal arteritis), Giant cell myocarditis, Glomerulonephritis, Goodpasture’s syndrome, Granulomatosis with Polyangiitis (GPA) (formerly called Wegener’s Granulomatosis), Graves’ disease, Guillain-Barre syndrome, Hashimoto’s encephalitis, Hashimoto’s thyroiditis, Hemolytic anemia, Henoch-Schonlein purpura, Herpes gestationis, Hypogammaglobulinemia, Idiopathic thrombocytopenic purpura (ITP), IgA nephropathy, IgG4-related sclerosing disease, Immunoregulatory lipoproteins, Inclusion body myositis, Interstitial cystitis, Juvenile arthritis, Juvenile diabetes (Type 1 diabetes), Juvenile myositis, Kawasaki syndrome, Lambert-Eaton syndrome, Leukocytoclastic vasculitis, Lichen planus, Lichen sclerosus, Ligneous conjunctivitis, Linear IgA disease (LAD), Lupus (SLE), Lyme disease, chronic, Meniere’s disease, Microscopic polyangiitis, Mixed connective tissue disease (MCTD), Mooren’s ulcer, Mucha-Habermann disease, Multiple sclerosis, Myasthenia gravis, Myositis, Narcolepsy, Neuromyelitis optica (Devic’s), Neutropenia, Ocular cicatricial pemphigoid, Optic neuritis, Palindromic rheumatism, PANDAS (Pediatric Autoimmune Neuropsychiatric Disorders Associated with Streptococcus), Paraneoplastic cerebellar degeneration, Paroxysmal nocturnal hemoglobinuria (PNH), Parry Romberg syndrome, Parsonnage-Turner syndrome, Pars planitis (peripheral uveitis), Pemphigus, Peripheral neuropathy, Perivenous encephalomyelitis, Pernicious anemia, POEMS syndrome, Polyarteritis nodosa, Type I, II, & III autoimmune polyglandular syndromes, Polymyalgia rheumatica, Polymyositis, Postmyocardial infarction syndrome, Postpericardiotomy syndrome, Progesterone dermatitis, Primary biliary cirrhosis, Primary sclerosing cholangitis, Psoriasis, Psoriatic arthritis, Idiopathic pulmonary fibrosis, Pyoderma gangrenosum, Pure red cell aplasia, Raynauds phenomenon, Reactive Arthritis, Reflex sympathetic dystrophy, Reiter’s syndrome, Relapsing polychondritis, Restless legs syndrome, Retroperitoneal fibrosis, Rheumatic fever, Rheumatoid arthritis, Sarcoidosis, Schmidt syndrome, Scleritis, Scleroderma, Sjogren’s syndrome, Sperm & testicular autoimmunity, Stiff person syndrome, Subacute bacterial endocarditis (SBE), Susac’s syndrome, Sympathetic ophthalmia, Takayasu’s arteritis, Temporal arteritis/Giant cell arteritis, Thrombocytopenic purpura (TTP), Tolosa-Hunt syndrome, Transverse myelitis, Type 1 diabetes, Ulcerative colitis, Undifferentiated connective tissue disease (UCTD), Uveitis, Vasculitis, Vesiculobullous dermatosis, Vitiligo, or Wegener’s granulomatosis (i.e., Granulomatosis with Polyangiitis (GPA).
As used herein, the term “inflammatory disease” refers to a disease or condition characterized by aberrant inflammation (e.g. an increased level of inflammation compared to a control such as a healthy person not suffering from a disease). Examples of inflammatory diseases include traumatic brain injury, arthritis, rheumatoid arthritis, psoriatic arthritis, juvenile idiopathic arthritis, multiple sclerosis, systemic lupus erythematosus (SLE), myasthenia gravis, juvenile onset diabetes, diabetes mellitus type 1, Guillain-Barre syndrome, Hashimoto’s encephalitis, Hashimoto’s thyroiditis, ankylosing spondylitis, psoriasis, Sjogren’s syndrome,vasculitis, glomerulonephritis, auto-immune thyroiditis, Behcet’s disease, Crohn’s disease, ulcerative colitis, bullous pemphigoid, sarcoidosis, ichthyosis, Graves ophthalmopathy, inflammatory bowel disease, Addison’s disease, Vitiligo, asthma, asthma, allergic asthma, acne vulgaris, celiac disease, chronic prostatitis, inflammatory bowel disease, pelvic inflammatory disease, reperfusion injury, sarcoidosis, transplant rejection, interstitial cystitis, atherosclerosis, and atopic dermatitis.
As used herein, the term “neurodegenerative disorder” or “neurodegenerative disease” refers to a disease or condition in which the function of a subject’s nervous system becomes impaired. Examples of neurodegenerative diseases that may be treated with a compound, pharmaceutical composition, or method described herein include Alexander’s disease, Alper’s disease, Alzheimer’s disease, Amyotrophic lateral sclerosis, Ataxia telangiectasia, Batten disease (also known as Spielmeyer-Vogt-Sjogren-Batten disease), Bovine spongiform encephalopathy (BSE), Canavan disease, chronic fatigue syndrome, Cockayne syndrome, Corticobasal degeneration, Creutzfeldt-Jakob disease, frontotemporal dementia, Gerstmann-Sträussler-Scheinker syndrome, Huntington’s disease, HIV-associated dementia, Kennedy’s disease, Krabbe’s disease, kuru, Lewy body disease, Lewy body dementia, Machado-Joseph disease (Spinocerebellar ataxia type 3), Multiple sclerosis, Multiple System Atrophy, myalgic encephalomyelitis, Narcolepsy, Neuroborreliosis, Parkinson’s disease, Pelizaeus-Merzbacher Disease, Pick’s disease, Primary lateral sclerosis, Prion diseases, Progressive Supranuclear Palsy, Refsum’s disease, Sandhoffs disease, Schilder’s disease, Subacute combined degeneration of spinal cord secondary to Pernicious Anaemia, Schizophrenia, Spinocerebellar ataxia (multiple types with varying characteristics), Spinal muscular atrophy, Steele-Richardson-Olszewski disease , progressive supranuclear palsy, or Tabes dorsalis.
The terms “treating”, or “treatment” refers to any indicia of success in the therapy or amelioration of an injury, disease, pathology or condition, including any objective or subjective parameter such as abatement; remission; diminishing of symptoms or making the injury, pathology or condition more tolerable to the patient; slowing in the rate of degeneration or decline; making the final point of degeneration less debilitating; improving a patient’s physical or mental well-being. The treatment or amelioration of symptoms can be based on objective or subjective parameters; including the results of a physical examination, neuropsychiatric exams, and/or a psychiatric evaluation. The term “treating” and conjugations thereof, may include prevention of an injury, pathology, condition, or disease. In embodiments, treating is preventing. In embodiments, treating does not include preventing.
“Treating” or “treatment” as used herein (and as well-understood in the art) also broadly includes any approach for obtaining beneficial or desired results in a subject’s condition, including clinical results. Beneficial or desired clinical results can include, but are not limited to, alleviation or amelioration of one or more symptoms or conditions, diminishment of the extent of a disease, stabilizing (i.e., not worsening) the state of disease, prevention of a disease’s transmission or spread, delay or slowing of disease progression, amelioration or palliation of the disease state, diminishment of the reoccurrence of disease, and remission, whether partial or total and whether detectable or undetectable. In other words, “treatment” as used herein includes any cure, amelioration, or prevention of a disease. Treatment may prevent the disease from occurring; inhibit the disease’s spread; relieve the disease’s symptoms (e.g., ocular pain, seeing halos around lights, red eye, very high intraocular pressure), fully or partially remove the disease’s underlying cause, shorten a disease’s duration, or do a combination of these things.
“Treating” and “treatment” as used herein include prophylactic treatment. Treatment methods include administering to a subject a therapeutically effective amount of an active agent. The administering step may consist of a single administration or may include a series of administrations. The length of the treatment period depends on a variety of factors, such as the severity of the condition, the age of the patient, the concentration of active agent, the activity of the compositions used in the treatment, or a combination thereof. It will also be appreciated that the effective dosage of an agent used for the treatment or prophylaxis may increase or decrease over the course of a particular treatment or prophylaxis regime. Changes in dosage may result and become apparent by standard diagnostic assays known in the art. In some instances, chronic administration may be required. For example, the compositions are administered to the subject in an amount and for a duration sufficient to treat the patient. In embodiments, the treating or treatment is not prophylactic treatment (e.g., the patient has a disease, the patient suffers from a disease).
The term “prevent” refers to a decrease in the occurrence of Caspase 6 disease symptoms in a patient. As indicated above, the prevention may be complete (no detectable symptoms) or partial, such that fewer symptoms are observed than would likely occur absent treatment.
“Patient” or “subject in need thereof” refers to a living organism suffering from or prone to a disease or condition that can be treated by administration of a pharmaceutical composition as provided herein. Non-limiting examples include humans, other mammals, bovines, rats, mice, dogs, monkeys, goat, sheep, cows, deer, and other non-mammalian animals. In some embodiments, a patient is human.
A “effective amount” is an amount sufficient for a compound to accomplish a stated purpose relative to the absence of the compound (e.g. achieve the effect for which it is administered, treat a disease, reduce enzyme activity, increase enzyme activity, reduce a signaling pathway, or reduce one or more symptoms of a disease or condition). An example of an “effective amount” is an amount sufficient to contribute to the treatment, prevention, or reduction of a symptom or symptoms of a disease, which could also be referred to as a “therapeutically effective amount.” A “reduction” of a symptom or symptoms (and grammatical equivalents of this phrase) means decreasing of the severity or frequency of the symptom(s), or elimination of the symptom(s). A “prophylactically effective amount” of a drug is an amount of a drug that, when administered to a subject, will have the intended prophylactic effect, e.g., preventing or delaying the onset (or reoccurrence) of an injury, disease, pathology or condition, or reducing the likelihood of the onset (or reoccurrence) of an injury, disease, pathology, or condition, or their symptoms. The full prophylactic effect does not necessarily occur by administration of one dose, and may occur only after administration of a series of doses. Thus, a prophylactically effective amount may be administered in one or more administrations. An “activity decreasing amount,” as used herein, refers to an amount of antagonist required to decrease the activity of an enzyme relative to the absence of the antagonist. A “function disrupting amount,” as used herein, refers to the amount of antagonist required to disrupt the function of an enzyme or protein relative to the absence of the antagonist. The exact amounts will depend on the purpose of the treatment, and will be ascertainable by one skilled in the art using known techniques (see, e.g., Lieberman, Pharmaceutical Dosage Forms (vols. 1-3, 1992); Lloyd, The Art, Science and Technology of Pharmaceutical Compounding (1999); Pickar, Dosage Calculations (1999); and Remington: The Science and Practice of Pharmacy, 20th Edition, 2003, Gennaro, Ed., Lippincott, Williams & Wilkins).
For any compound described herein, the therapeutically effective amount can be initially determined from cell culture assays. Target concentrations will be those concentrations of active compound(s) that are capable of achieving the methods described herein, as measured using the methods described herein or known in the art.
As is well known in the art, therapeutically effective amounts for use in humans can also be determined from animal models. For example, a dose for humans can be formulated to achieve a concentration that has been found to be effective in animals. The dosage in humans can be adjusted by monitoring compounds effectiveness and adjusting the dosage upwards or downwards, as described above. Adjusting the dose to achieve maximal efficacy in humans based on the methods described above and other methods is well within the capabilities of the ordinarily skilled artisan.
The term “therapeutically effective amount,” as used herein, refers to that amount of the therapeutic agent sufficient to ameliorate the disorder, as described above. For example, for the given parameter, a therapeutically effective amount will show an increase or decrease of at least 5%, 10%, 15%, 20%, 25%, 40%, 50%, 60%, 75%, 80%, 90%, or at least 100%. Therapeutic efficacy can also be expressed as “-fold” increase or decrease. For example, a therapeutically effective amount can have at least a 1.2-fold, 1.5-fold, 2-fold, 5-fold, or more effect over a control.
Dosages may be varied depending upon the requirements of the patient and the compound being employed. The dose administered to a patient, in the context of the present disclosure, should be sufficient to effect a beneficial therapeutic response in the patient over time. The size of the dose also will be determined by the existence, nature, and extent of any adverse side-effects. Determination of the proper dosage for a particular situation is within the skill of the practitioner. Generally, treatment is initiated with smaller dosages which are less than the optimum dose of the compound. Thereafter, the dosage is increased by small increments until the optimum effect under circumstances is reached. Dosage amounts and intervals can be adjusted individually to provide levels of the administered compound effective for the particular clinical indication being treated. This will provide a therapeutic regimen that is commensurate with the severity of the individual’s disease state.
As used herein, the term “administering” means oral administration, administration as a suppository, topical contact, intravenous, parenteral, intraperitoneal, intramuscular, intralesional, intrathecal, intranasal or subcutaneous administration, or the implantation of a slow-release device, e.g., a mini-osmotic pump, to a subject. Administration is by any route, including parenteral and transmucosal (e.g., buccal, sublingual, palatal, gingival, nasal, vaginal, rectal, or transdermal). Parenteral administration includes, e.g., intravenous, intramuscular, intra-arteriole, intradermal, subcutaneous, intraperitoneal, intraventricular, and intracranial. Other modes of delivery include, but are not limited to, the use of liposomal formulations, intravenous infusion, transdermal patches, etc. In embodiments, the administering does not include administration of any active agent other than the recited active agent.
“Co-administer” it is meant that a composition described herein is administered at the same time, just prior to, or just after the administration of one or more additional therapies. The compounds provided herein can be administered alone or can be coadministered to the patient. Coadministration is meant to include simultaneous or sequential administration of the compounds individually or in combination (more than one compound). Thus, the preparations can also be combined, when desired, with other active substances (e.g. to reduce metabolic degradation). The compositions of the present disclosure can be delivered transdermally, by a topical route, or formulated as applicator sticks, solutions, suspensions, emulsions, gels, creams, ointments, pastes, jellies, paints, powders, and aerosols.
A “cell” as used herein, refers to a cell carrying out metabolic or other function sufficient to preserve or replicate its genomic DNA. A cell can be identified by well-known methods in the art including, for example, presence of an intact membrane, staining by a particular dye, ability to produce progeny or, in the case of a gamete, ability to combine with a second gamete to produce a viable offspring. Cells may include prokaryotic and eukaroytic cells. Prokaryotic cells include but are not limited to bacteria. Eukaryotic cells include but are not limited to yeast cells and cells derived from plants and animals, for example mammalian, insect (e.g., spodoptera) and human cells. Cells may be useful when they are naturally nonadherent or have been treated not to adhere to surfaces, for example by trypsinization.
“Control” or “control experiment” is used in accordance with its plain ordinary meaning and refers to an experiment in which the subjects or reagents of the experiment are treated as in a parallel experiment except for omission of a procedure, reagent, or variable of the experiment. In some instances, the control is used as a standard of comparison in evaluating experimental effects. In some embodiments, a control is the measurement of the activity of a protein in the absence of a compound as described herein (including embodiments and examples).
The term “irreversible covalent bond” is used in accordance with its plain ordinary meaning in the art and refers to the resulting association between atoms or molecules of (e.g., electrophilic chemical moiety and nucleophilic moiety) wherein the probability of dissociation is low. In embodiments, the irreversible covalent bond does not easily dissociate under normal biological conditions. In embodiments, the irreversible covalent bond is formed through a chemical reaction between two species (e.g., electrophilic chemical moiety and nucleophilic moiety).
The term “electrophilic moiety” is used in accordance with its plain ordinary chemical meaning and refers to a chemical group (e.g., monovalent chemical group) that is electrophilic. In embodiments, the electrophilic chemical moiety is referred to herein as a “warhead” or “E.” In embodiments, E is:
, wherein R14, R15, R16, R17, R18, R19, and R20 are as described herein, including in embodiments. X17 is —F, C1, —Br, or —I. In embodiments, an electrophilic moiety is a covalent cysteine modifier moiety.
The term “covalent cysteine modifier moiety” as used herein refers to a monovalent electrophilic moiety that is able to measurably bind to a cysteine amino acid. In embodiments, the covalent cysteine modifier moiety binds via an irreversible covalent bond. In embodiments, the covalent cysteine modifier moiety is capable of binding with a Kd of less than about 10 µM, 5 µM, 1 µM, 500 nM, 250 nM, 100 nM, 75 nM, 50 nM, 25 nM, 15 nM, 10 nM, 5 nM, 1 nM, or about 0.1 nM. In embodiments, the covalent cysteine modifier moiety binds via a covalent bond.
The term “nucleophilic moiety” is used in accordance with its plain ordinary chemical meaning and refers to a chemical group (e.g., monovalent chemical group) that is nucleophilic.
An amino acid residue in a protein “corresponds” to a given residue when it occupies the same essential structural position within the protein as the given residue. Instead of a primary sequence alignment, a three-dimensional structural alignment can also be used, e.g., where the structure of the selected protein is aligned for maximum correspondence with the human protein and the overall structures compared. In this case, an amino acid that occupies the same essential position as a specified amino acid in the structural model is said to correspond to the specified residue. For example, a selected residue in a selected protein corresponds to C264 of a Caspase 6 protein (e.g., human Caspase 6 protein) when the selected residue occupies the same essential spatial or other structural relationship as C264 in the Caspase 6 protein (e.g., human Caspase 6 protein). In some embodiments, where a selected protein is aligned for maximum homology with the Caspase 6 protein (e.g., human Caspase 6 protein), the position in the aligned selected protein aligning with C264 is said to correspond to C264 of the Caspase 6 protein (e.g., human Caspase 6 protein). Instead of a primary sequence alignment, a three dimensional structural alignment can also be used, e.g., where the structure of the selected protein is aligned for maximum correspondence with the Caspase 6 protein (e.g., human Caspase 6 protein or SEQ ID NO: 1) and the overall structures compared. In this case, an amino acid that occupies the same essential position as C264 of a Caspase 6 protein (e.g., human Caspase 6 protein) in the structural model is said to correspond to the C264 residue. Another example is wherein a selected residue in a selected protein corresponds to C264 in a Caspase 6 protein (e.g., human Caspase 6 protein) when the selected residue (e.g., cysteine residue) occupies essential the same sequence, spatial, or other structural position within the protein as C264 in the Caspase 6 protein (e.g., human Caspase 6 protein).
The term “amino acid” refers to naturally occurring and synthetic amino acids, as well as amino acid analogs and amino acid mimetics that function in a manner similar to the naturally occurring amino acids. Naturally occurring amino acids are those encoded by the genetic code, as well as those amino acids that are later modified, e.g., hydroxyproline, γ-carboxyglutamate, and O-phosphoserine. Amino acid analogs refers to compounds that have the same basic chemical structure as a naturally occurring amino acid, i.e., an α carbon that is bound to a hydrogen, a carboxyl group, an amino group, and an R group, e.g., homoserine, norleucine, methionine sulfoxide, methionine methyl sulfonium. Such analogs have modified R groups (e.g., norleucine) or modified peptide backbones, but retain the same basic chemical structure as a naturally occurring amino acid. Amino acid mimetics refers to chemical compounds that have a structure that is different from the general chemical structure of an amino acid, but that functions in a manner similar to a naturally occurring amino acid. The terms “non-naturally occurring amino acid” and “unnatural amino acid” refer to amino acid analogs, synthetic amino acids, and amino acid mimetics which are not found in nature.
Amino acids may be referred to herein by either their commonly known three letter symbols or by the one-letter symbols recommended by the IUPAC-IUB Biochemical Nomenclature Commission. Nucleotides, likewise, may be referred to by their commonly accepted single-letter codes.
The terms “polypeptide,” “peptide,” and “protein” are used interchangeably herein to refer to a polymer of amino acid residues, wherein the polymer may in embodiments be conjugated to a moiety that does not consist of amino acids. The terms apply to amino acid polymers in which one or more amino acid residue is an artificial chemical mimetic of a corresponding naturally occurring amino acid, as well as to naturally occurring amino acid polymers and non-naturally occurring amino acid polymers.
An amino acid or nucleotide base “position” is denoted by a number that sequentially identifies each amino acid (or nucleotide base) in the reference sequence based on its position relative to the N-terminus (or 5’-end). Due to deletions, insertions, truncations, fusions, and the like that must be taken into account when determining an optimal alignment, in general the amino acid residue number in a test sequence determined by simply counting from the N-terminus will not necessarily be the same as the number of its corresponding position in the reference sequence. For example, in a case where a variant has a deletion relative to an aligned reference sequence, there will be no amino acid in the variant that corresponds to a position in the reference sequence at the site of deletion. Where there is an insertion in an aligned reference sequence, that insertion will not correspond to a numbered amino acid position in the reference sequence. In the case of truncations or fusions there can be stretches of amino acids in either the reference or aligned sequence that do not correspond to any amino acid in the corresponding sequence.
The terms “numbered with reference to” or “corresponding to,” when used in the context of the numbering of a given amino acid or polynucleotide sequence, refers to the numbering of the residues of a specified reference sequence when the given amino acid or polynucleotide sequence is compared to the reference sequence.
In an aspect is provided a compound having the formula:
or
In an aspect, provided herein are compounds of formulae (I), (II) and/or (III), including embodiments thereof, or metabolites thereof.
R1 is independently halogen, —CX13, —CHX12, —CH2X1, —OCX13, —OCH2X1, —OCHX12, —CN, —SOn1R1D, —SOv1NR1AR1B, —NR1CNR1AR1B, —ONR1AR1B, —NHC(O)NR1CNR1AR1B, —NHC(O)NR1AR1B, —N(O)m1, —NR1AR1B, —C(O)R1C, —C(O)—OR1C, —C(O) NR1AR1B, —OR1D, —NR1ASO2R1D, —NR1AC(O)R1C, —NR1AC(O)OR1C, —NR1AOR1C, —SF5, —N3, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl; two adjacent R1 substituents on adjacent carbons may optionally be joined to form a substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl or two R1 substituents bonded to the same carbon atom may optionally be joined to form a substituted or unsubstituted alkyl or substituted or unsubstituted heterocycloalkyl.
z1 is an integer from 0 to 9.
R2 is independently oxo, halogen, —CX23, —CHX22, —CH2X2, —OCX23, —OCH2X2, —OCHX22, —CN, —SOn2R2D, —SOv2NR2AR2B, —NR2CNR2AR2B, —ONR2AR2B, —NHC(O)NR2CNR2AR2B,—NHC(O)NR2AR2B, —N(O)m2, —NR2AR2B, —C(O)R2C, —C(O)—OR2C, —C(O) NR2AR2B, —OR2D, —NR2ASO2R2D, —NR2AC(O)R2C, —NR2AC(O)OR2C, —NR2AOR2C, —SF5, —N3, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl; two adjacent R2 substituents on adjacent carbons may optionally be joined to form a substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted phenyl, or substituted or unsubstituted heteroaryl.
z2 is an integer from 0 to 6.
L3 is a bond, —S(O)2—, —NR3—, —NH—, —O—, —S—, —C(O)—, —C(O)NR3—, —NR3C(O)—, —N(R3)CH2—, —NR3C(O)NH —, —NHC(O)NR3—, —C(O)O—, —OC(O)—, substituted or unsubstituted alkylene, or substituted or unsubstituted heteroalkylene.
L4 is a bond, —NH—, —NR4—, or substituted or unsubstituted alkylene.
L6 is —N(R6)—L3— or —C(O)NH—.
W5 is CH or N.
z6 is 1 or 2.
R3, R4, and R6 are independently hydrogen, —CC13, —CBr3, —CF3, —CI3, CHC12, —CHBr2, —CHF2, —CHI2, —CH2C1, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CO(C1-C6 alkyl), —CONH2, —OCC13, —OCF3, —OCBr3, —OCI3, —OCHC12, —OCHBr2, —OCHI2, —OCHF2, —OCH2 C1, —OCH2Br, —OCH2I, —OCH2F, unsubstituted alkyl, unsubstituted heteroalkyl, unsubstituted cycloalkyl, or unsubstituted heterocycloalkyl.
R7, R8, R9, and R10 are independently hydrogen or unsubstituted C1-C10 alkyl.
Ring B is aryl or heteroaryl.
R5 is an electrophilic moiety.
R1A, R1B, R1C, R1D, R2A, R2B, R2C, and R2D are independently hydrogen, —CC13, —CBr3, —CF3, —CI3, CHC12, —CHBr2, —CHF2, —CHI2, —CH2C1, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCC13, —OCF3, —OCBr3, —O CI3, —OCHC12, —OCHBr2, —OCHI2, —OCHF2, —OCH2C1, —OCH2Br, —OCH2I, —OCH2F, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl; R1A and R1B substituents bonded to the same nitrogen atom may optionally be joined to form a substituted or unsubstituted heterocycloalkyl or substituted or unsubstituted heteroaryl; R2A and R2B substituents bonded to the same nitrogen atom may optionally be joined to form a substituted or unsubstituted heterocycloalkyl or substituted or unsubstituted heteroaryl.
X1 and X2 are independently —F, —Cl, —Br, or —I.
n1 and n2 are independently an integer from 0 to 4.
m1, m2, v1, and v2 are independently 1 or 2.
In embodiments, is provided a compound having the formula:
Ring B, R1, z1, R2, z2, R5, L3, L4, L6, z6, and W5 are as described herein, including in embodiments. In embodiments, is provided a compound having the formula:
Ring B, R1, z1, R2, z2, R5, L3, L4, z6, and W5 are as described herein, including in embodiments. In embodiments, is provided a compound having the formula:
Ring B, R2, z2, R5, L4, and L6 are as described herein, including in embodiments. In embodiments, is provided a compound having the formula:
Ring B, R2, z2, R5, R7, R8, R9, R10, L4, and L6 are as described herein, including in embodiments.
In embodiments, R3, R4, and R6 are independently hydrogen, —CC13, —CBr3, —CF3, —CI3, CHC12, —CHBr2, —CHF2, —CHI2, —CH2C1, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —COCH3, —CONH2, —OCC13, —OCF3, —OCBr3, —OCI3, —OCHC12, —OCHBr2, —OCHI2, —OCHF2, —OC H2C1, —OCH2Br, —OCH2I, —OCH2F, unsubstituted alkyl, unsubstituted heteroalkyl, unsubstituted cycloalkyl, or unsubstituted heterocycloalkyl.
In embodiments, R3, R4, and R6 are independently hydrogen, —CC13, —CBr3, —CF3, —CI3, CHC12, —CHBr2, —CHF2, —CHI2, —CH2C1, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCC13, —OCF3, —OCBr3, —O CI3, —OCHC12, —OCHBr2, —OCHI2, —OCHF2, —OCH2C1, —OCH2Br, —OCH2I, —OCH2F, unsubstituted alkyl, or unsubstituted heteroalkyl.
In embodiments, the electrophilic moiety is a covalent cysteine modifier moiety. In embodiments, R5 is a covalent cysteine modifier moiety.
In embodiments, R5 is independently
R14 is independently ═O or ═NR19.
R15 is independently ═O or ═NR20.
R16, R17, and R18 are independently hydrogen, oxo, halogen, —CC13, —CBr3, —CF3, —CI3, CHC12, —CHBr2, —CHF2, —CHI2, —CH2C1, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —C(O)N(CH3)2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCC13, —OCF3, —OCBr3, —OCI3, —OCHC12, —OCHBr2, —OCHI2, —OCHF2, —OCH2C1, —OCH2Br, —OCH2I, —OCH2F, —N3, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl.
R19 and R20 are independently hydrogen, —CC13, —CBr3, —CF3, —CI3, CHC12, —CHBr2, —CHF2, —CHI2, —CH2C1, —CH2Br, —CH2F, —CH2I, —CN, —COOH, —CONH2, —C(O)N(CH3)2, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl.
In embodiments is provided a compound having the formula:
or
R1 is independently halogen, —CX13, —CHX12, —CH2X1, —OCX13, —OCH2X1, —OCHX12, —CN, —SOn1R1D, —SOv1NR1AR1B, —NR1CNR1AR1B, —ONR1AR1B, —NHC(O)NR1CNR1AR1B, —NHC(O)NR1AR1B, —N(O)m1, —NR1AR1B, —C(O)R1C, —C(O)—OR1C, —C(O) NR1AR1B, —OR1D, —NR1ASO2R1D, —NR1AC(O)R1C, —NR1AC(O)OR1C, —NR1AOR1C, —SF5, —N3, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl; two adjacent R1 substituents on adjacent carbons may optionally be joined to form a substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl or two R1 substituents bonded to the same carbon atom may optionally be joined to form a substituted or unsubstituted alkyl or substituted or unsubstituted heterocycloalkyl; z1 is an integer from 0 to 9; R2 is independently oxo, halogen, —CX23, —CHX22, —CH2X2, —OCX23, —OCH2X2, —OCHX22, —CN, —SOn2R2D, —SOv2NR2AR2B, —NR2CNR2AR2B, —ONR2AR2B, —NHC(O)NR2CNR2AR2B,—NHC(O)NR2AR2B, —N(O)m2, —NR2AR2B, —C(O)R2C, —C(O)—OR2C, —C(O) NR2AR2B, —OR2D, —NR2ASO2R2D, —NR2AC(O)R2C, —NR2AC(O)OR2C, —NR2AOR2C, —SF5, —N3, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl; two adjacent R2 substituents on adjacent carbons may optionally be joined to form a substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted phenyl, or substituted or unsubstituted heteroaryl; z2 is an integer from 0 to 6; L3 is a bond, —S(O)2—, —NR3—, —NH—, —O—, —S—, —C(O)—, —C(O)NR3—, —NR3C(O)—, —N(R3)CH2—, —NR3C(O)NH —, —NHC(O)NR3—, —C(O)O—, —OC(O)—, substituted or unsubstituted alkylene, or substituted or unsubstituted heteroalkylene; L4 is a bond, —NH—, —NR4—, or substituted or unsubstituted alkylene; L6 is —N(R6)—L3— or —C(O)NH—; W5 is CH or N; z6 is 1 or 2; R3, R4, and R6 are independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CO(C1-C6 alkyl), —CONH2, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2 Cl, —OCH2Br, —OCH2I, —OCH2F, unsubstituted alkyl, unsubstituted heteroalkyl, unsubstituted cycloalkyl, or unsubstituted heterocycloalkyl; R7, R8, R9, and R10 are independently hydrogen or unsubstituted C1-C10 alkyl; Ring B is aryl or heteroaryl; R5 is independently
; wherein, R14 is independently =O or ═NR19; R15 is independently =O or =NR20; R16, R17, and R18 are independently hydrogen, oxo, halogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —C(O)N(CH3)2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, —N3, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl; R19 and R20 are independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —COOH, —CONH2, —C(O)N(CH3)2, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl; R1A, R1B, R1C, R1D, R2A, R2B, R2C, and R2D are independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl; R1A and R1B substituents bonded to the same nitrogen atom may optionally be joined to form a substituted or unsubstituted heterocycloalkyl or substituted or unsubstituted heteroaryl; R2A and R2B substituents bonded to the same nitrogen atom may optionally be joined to form a substituted or unsubstituted heterocycloalkyl or substituted or unsubstituted heteroaryl; X1 and X2 are independently —F, —Cl, —Br, or —I; n1 and n2 are independently an integer from 0 to 4; and m1, m2, v1, and v2 are independently 1 or 2.
In embodiments, R5 is independently
wherein R16, R17, and R18, are as described herein, including in embodiments.
In embodiments, R5 is independently
In embodiments is provided a compound having the formula:
or
R1 is independently halogen, -CX13, -CHX12, -CH2X1, —OCX13, —OCH2X1, —OCHX12, —CN, —SOn1R1D, —SOv1NR1AR1B, —NR1CNR1AR1B, —ONR1AR1B, —NHC(O)NR1CNR1AR1B, —NHC(O)NR1AR1B, —N(O)m1, —NR1AR1B, —C(O)R1C, —C(O)—OR1C, —C(O) NR1AR1B, —OR1D, —NR1ASO2R1D, —NR1AC(O)R1C, —NR1AC(O)OR1C, —NR1AOR1C, —SF5, —N3, substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted C6-C10 aryl, or substituted or unsubstituted 5 to 10 membered heteroaryl; two adjacent R1 substituents on adjacent carbons may optionally be joined to form a substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted phenyl, or substituted or unsubstituted 5 to 6 membered heteroaryl; or two R1 substituents bonded to the same carbon atom may optionally be joined to form a substituted or unsubstituted C3-C6 cycloalkyl or substituted or unsubstituted 3 to 6 membered heterocycloalkyl; z1 is an integer from 0 to 9; R2 is independently oxo, halogen, —CX23, —CHX22, —CH2X2, —OCX23, —OCH2X2, —OCHX22, —CN, —SOn2R2D, —SOv2NR2AR2B, —NR2CNR2AR2B, —ONR2AR2B, —NHC(O)NR2CNR2AR2B,—NHC(O)NR2AR2B, —N(O)m2, —NR2AR2B, —C(O)R2C, —C(O)—OR2C, —C(O) NR2AR2B, —OR2D, —NR2ASO2R2D, —NR2AC(O)R2C, —NR2AC(O)OR2C, —NR2AOR2C, —SF5, —N3, substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted C6-C10 aryl, or substituted or unsubstituted 5 to 10 membered heteroaryl; two adjacent R2 substituents on adjacent carbons may optionally be joined to form a substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted phenyl, or substituted or unsubstituted 5 to 6 membered heteroaryl; z2 is an integer from 0 to 6; L3 is a bond, —S(O)2—, —NR3—, —NH—, —O—, —S—, —C(O)—, —C(O)NR3—, —NR3C(O)—, —N(R3)CH2—, —NR3C(O)NH —, —NHC(O)NR3—, —C(O)O—, —OC(O)—, substituted or unsubstituted C1-C6 alkylene, or substituted or unsubstituted 2 to 6 membered heteroalkylene; L4 is a bond, —NH—, —NR4—, or substituted or unsubstituted C1-C2 alkylene; L6 is —N(R6)—L3— or —C(O)NH—; W5 is CH or N; z6 is 1 or 2; R3, R4, and R6 are independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —COCH3, —CONH2, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OC H2Cl, —OCH2Br, —OCH2I, —OCH2F, unsubstituted C1-C6 alkyl, unsubstituted 2 to 6 membered heteroalkyl, unsubstituted cycloalkyl, or unsubstituted heterocycloalkyl; R7, R8, R9, and R10 are independently hydrogen or unsubstituted C1-C10 alkyl; Ring B is C6-C10 aryl, or 5 to 10 membered heteroaryl; R5 is independently
R14 is independently =O or ═NR19; R15 is independently =O or ═NR20; R16, R17, and R18 are independently hydrogen, oxo, halogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —C(O)N(CH3)2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, —N3, substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted C6-C12 aryl, or substituted or unsubstituted 5 to 12 membered heteroaryl; R19 and R20 are independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —COOH, —CONH2, —C(O)N(CH3)2, substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted C6-C12 aryl, or substituted or unsubstituted 5 to 12 membered heteroaryl; R1A, R1B, R1C, R1D, R2A, R2B, R2C, and R2D are independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl; R1A and R1B substituents bonded to the same nitrogen atom may optionally be j oined to form a substituted or unsubstituted heterocycloalkyl or substituted or unsubstituted heteroaryl; R2A and R2B substituents bonded to the same nitrogen atom may optionally be joined to form a substituted or unsubstituted heterocycloalkyl or substituted or unsubstituted heteroaryl; X1 and X2 are independently —F, —Cl, —Br, or —I; n1 and n2 are independently an integer from 0 to 4; and m1, m2, v1, and v2 are independently 1 or 2.
In embodiments is provided a compound having the formula:
or
R1 is independently halogen, —CX13, —CHX12, —CH2X1, —OCX13, —OCH2X1, —OCHX12, —CN, —SOn1R1D, —SOv1NR1AR1B, —NR1CNR1AR1B, —ONR1AR1B, —NHC(O)NR1CNR1AR1B, —NHC(O)NR1AR1B, —N(O)m1, —NR1AR1B, —C(O)R1C, —C(O)—OR1C, —C(O) NR1AR1B, —OR1D, —NR1ASO2R1D, —NR1AC(O)R1C, —NR1AC(O)OR1C, —NR1AOR1C, —SF5, —N3, substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted C6-C10 aryl, or substituted or unsubstituted 5 to 10 membered heteroaryl; two adjacent R1 substituents on adjacent carbons may optionally be joined to form a substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted phenyl, or substituted or unsubstituted 5 to 6 membered heteroaryl; or two R1 substituents bonded to the same carbon atom may optionally be joined to form a substituted or unsubstituted C3-C6 cycloalkyl or substituted or unsubstituted 3 to 6 membered heterocycloalkyl; z1 is an integer from 0 to 9; R2 is independently oxo, halogen, —CX23, —CHX22, —CH2X2, —OCX23, —OCH2X2, —OCHX22, —CN, —SOn2R2D, —SOv2NR2AR2B, —NR2CNR2AR2B, —ONR2AR2B, —NHC(O)NR2CNR2AR2B,—NHC(O)NR2AR2B, —N(O)m2, —NR2AR2B, —C(O)R2C, —C(O)—OR2C, —C(O) NR2AR2B, —OR2D, —NR2ASO2R2D, —NR2AC(O)R2C, —NR2AC(O)OR2C, —NR2AOR2C, —SF5, —N3, substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted C6-C10 aryl, or substituted or unsubstituted 5 to 10 membered heteroaryl; two adjacent R2 substituents on adjacent carbons may optionally be joined to form a substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted phenyl, or substituted or unsubstituted 5 to 6 membered heteroaryl; z2 is an integer from 0 to 6; L3 is a bond, —S(O)2—, —NR3—, —NH—, —O—, —S—, —C(O)—, —C(O)NR3—, —NR3C(O)—, —N(R3)CH2—, —NR3C(O)NH —, —NHC(O)NR3—, —C(O)O—, —OC(O)—, substituted or unsubstituted C1-C6 alkylene, or substituted or unsubstituted 2 to 6 membered heteroalkylene; L4 is a bond, —NH—, —NR4—, or substituted or unsubstituted C1-C2 alkylene; L6 is —N(R6)—L3— or —C(O)NH—; W5 is CH or N; z6 is 1 or 2; R3, R4, and R6 are independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, unsubstituted C1-C6 alkyl, or unsubstituted 2 to 6 membered heteroalkyl; Ring B is C6-C10 aryl, or 5 to 10 membered heteroaryl; R5 is independently
R16, R17, and R18 are independently hydrogen, oxo, halogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —C(O)N(CH3)2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, —N3, substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted C6-C12 aryl, or substituted or unsubstituted 5 to 12 membered heteroaryl; R1A, R1B, R1C, R1D, R2A, R2B, R2C, and R2D are independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl; R1A and R1B substituents bonded to the same nitrogen atom may optionally be joined to form a substituted or unsubstituted heterocycloalkyl or substituted or unsubstituted heteroaryl; R2A and R2B substituents bonded to the same nitrogen atom may optionally be joined to form a substituted or unsubstituted heterocycloalkyl or substituted or unsubstituted heteroaryl; X1 and X2 are independently —F, —Cl, —Br, or —I; n1 and n2 are independently an integer from 0 to 4; and m1, m2, v1, and v2 are independently 1 or 2.
In embodiments is provided a compound having the formula:
or
R1 is independently halogen, —CX13, —CHX12, —CH2X1, —OCX13, —OCH2X1, —OCHX12, —CN, —SOn1R1D, —SOv1NR1AR1B, —NR1CNR1AR1B, —ONR1AR1B, —NHC(O)NR1CNR1AR1B, —NHC(O)NR1AR1B, —N(O)m1, —NR1AR1B, —C(O)R1C, —C(O)—OR1C, —C(O) NR1AR1B, —OR1D, —NR1ASO2R1D, —NR1AC(O)R1C, —NR1AC(O)OR1C, —NR1AOR1C, —SF5, —N3, substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted C6-C10 aryl, or substituted or unsubstituted 5 to 10 membered heteroaryl; two adjacent R1 substituents on adjacent carbons may optionally be joined to form a substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted phenyl, or substituted or unsubstituted 5 to 6 membered heteroaryl; or two R1 substituents bonded to the same carbon atom may optionally be joined to form a substituted or unsubstituted C3-C6 alkyl or substituted or unsubstituted 3 to 6 membered heterocycloalkyl; z1 is an integer from 0 to 9; R2 is independently oxo, halogen, —CX23, —CHX22, —CH2X2, —OCX23, —OCH2X2, —OCHX22, —CN, —SOn2R2D, —SOv2NR2AR2B, —NR2CNR2AR2B, —ONR2AR2B, —NHC(O)NR2CNR2AR2B,—NHC(O)NR2AR2B, —N(O)m2, —NR2AR2B, —C(O)R2C, —C(O)—OR2C, —C(O) NR2AR2B, —OR2D, —NR2ASO2R2D, —NR2AC(O)R2C, -NR2AC(O)OR2C, —NR2AOR2C, —SF5, —N3, substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted C6-C10 aryl, or substituted or unsubstituted 5 to 10 membered heteroaryl; two adjacent R2 substituents on adjacent carbons may optionally be joined to form a substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted phenyl, or substituted or unsubstituted 5 to 6 membered heteroaryl; z2 is an integer from 0 to 6; L3 is a bond, —S(O)2—, —NR3—, —NH—, —O—, —S—, —C(O)—, —C(O)NR3—, —NR3C(O)—, —N(R3)CH2—, —NR3C(O)NH —, —NHC(O)NR3—, —C(O)O—, —OC(O)—, substituted or unsubstituted C1-C6 alkylene, or substituted or unsubstituted 2 to 6 membered heteroalkylene; L4 is a bond, —NH—, —NR4—, or substituted or unsubstituted C1-C2 alkylene; L6 is —N(R6)—L3— or —C(O)NH—; W5 is CH or N; z6 is 1 or 2; R3, R4, and R6 are independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, unsubstituted C1-C6 alkyl, or unsubstituted 2 to 6 membered heteroalkyl; Ring B is C6-C10 aryl, or 5 to 10 membered heteroaryl; R5 is independently
R16, R17, and R18 are independently hydrogen, oxo, halogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —C(O)N(CH3)2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, —N3, substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted C6-C12 aryl, or substituted or unsubstituted 5 to 12 membered heteroaryl; R1A, R1B, R1C, R1D, R2A, R2B, R2C, and R2D are independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl; R1A and R1B substituents bonded to the same nitrogen atom may optionally be joined to form a substituted or unsubstituted heterocycloalkyl or substituted or unsubstituted heteroaryl; R2A and R2B substituents bonded to the same nitrogen atom may optionally be joined to form a substituted or unsubstituted heterocycloalkyl or substituted or unsubstituted heteroaryl; X1 and X2 are independently —F, —Cl, —Br, or —I; n1 and n2 are independently an integer from 0 to 4; and m1, m2, v1, and v2 are independently 1 or 2.
In embodiments, the compound has the formula
wherein R1, R2, R5, z1, z2, L3, L4, and Ring B are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, and R1.5 can be hydrogen or any value of R1, as described herein, including embodiments..
In embodiments, R1.2 and R1.3 are independently hydrogen, halogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, —N3, substituted or unsubstituted alkyl, or substituted or unsubstituted heteroalkyl; or R1.2 and R1.3 substituents on adjacent carbons may optionally be joined to form a substituted or unsubstituted phenyl, or substituted or unsubstituted heteroaryl.
In embodiments, R1.2 and R1.3 are independently hydrogen, halogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, —N3, substituted or unsubstituted C1-C6 alkyl, or substituted or unsubstituted 2 to 6 membered heteroalkyl; or R1.2 and R1.3 substituents on adjacent carbons may optionally be joined to form a substituted or unsubstituted phenyl, or substituted or unsubstituted 5 to 6 membered heteroaryl.
In embodiments, R1.4 and R1.5 are independently hydrogen, halogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, —N3, substituted or unsubstituted alkyl, or substituted or unsubstituted heteroalkyl.
In embodiments, R1.4 and R1.5 are independently hydrogen, halogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, —N3, substituted or unsubstituted C1-C6 alkyl, or substituted or unsubstituted 2 to 6 membered heteroalkyl.
In embodiments, the compound has the formula:
wherein R1.2, R1.3, R1.4, R1.5, R2, z2, R5, L3, and L4are as described herein, including in embodiments.
W1 is independently —O—, —NH—, or —NR2—.
W2 and W3 are independently ═N—, ═CH—, or ═CR2—.
R11 is independently oxo, halogen, —CX113, —CHX112, —CH2X11, —OCX113, —OCH2X11, —OCHX112, —CN, —OH, —NH2, —COOH, —CONH2, —C(O)N(CH3)2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —N3, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl.
R21 is independently oxo, halogen, —CX213, —CHX212, —CH2X21, —OCX213, —OCH2X21, —OCHX212, —CN, —OH, —NH2, —COOH, —CONH2, —C(O)N(CH3)2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —N3, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl.
X11 and X21 are independently —F, —Cl, —Br, or —I.
z11 is an integer from 0 to 4.
z21 is an integer from 0 to 5.
In embodiments, R2 is independently oxo, halogen, —CX23, —CHX22, —CH2X2, —OCX23, —OCH2X2, —OCHX22, —CN, —OH, —NH2, -COOH, —CONH2, —C(O)N(CH3)2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, SF5, —N3, substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted C6-C12 aryl, or substituted or unsubstituted 5 to 12 membered heteroaryl.
In embodiments, R2 is independently halogen, —OCX23, —OCH2X2, —OCHX22, unsubstituted C1-C3 alkyl, or unsubstituted 5 to 6 membered heteroaryl; R11 is independently halogen, —OCX113, —OCH2X11, -OCHX112, unsubstituted C1-C3 alkyl, or unsubstituted 5 to 6 membered heteroaryl; and R21 is independently halogen, —OCX213, —OCH2X21, —OCHX212, unsubstituted C1-C3 alkyl, or unsubstituted 5 to 6 membered heteroaryl.
In embodiments, R1.2, R1.3, R1.4 and R1.5 are independently hydrogen or halogen.
In embodiments, the compound has the formula:
wherein R1.2, R1.3 R1.4, R1.5, R2, z2, R21, z21, R5, L3, L4, W1, W2, and W3 are as described herein, including in embodiments. In embodiments, the compound has the formula:
wherein R1.2, R1.3, R1.4, R1.5, R2, z2, R5, L3, L4, W1, and W2, are as described herein, including in embodiments. In embodiments, the compound has the formula:
wherein R1.2, R1.3, R1.4, R1.5, R2, z2, R5, L3, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
wherein R1.4, R1.5, R2, z2, R5, R11, z11, L3, and L4 are as described herein, including in embodiments.
In embodiments, L3 is —C(O)—, —CH2—, —C(O)NH—, —NHC(O)—, —NHCH2—, —CH2CH2NH—, —C(O)CH2NH—, or —CH2C(O)NH—.
In embodiments, L4 is a bond, —NH—, or —CH2—. In embodiments, L4 is —NH—, —NR4—, or —CH2—. In embodiments, L4 is a bond. In embodiments, L4 is —NH—. In embodiments, L4 is —NR4—. In embodiments, L4 is —CH2—.
In embodiments, R5 is independently
wherein R16, R17, and R18, are as described herein, including in embodiments.
In embodiments, R16, R17, and R18 are independently hydrogen, —C(O)N(CH3)2, or unsubstituted C1-C3 alkyl.
In embodiments, R5 is independently
or
wherein R16, R17, and R18 are independently hydrogen, —C(O)N(CH3)2, or unsubstituted C1-C3 alkyl.
In embodiments, R5 is independently
wherein R16, R17, and R18 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R5, R11, z11, W1, W2, L3, and L4 are as described herein, including in embodiments. R2.1 and R2.2 are independently hydrogen or any value of R2, as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2.1, R2.2, R5, W1, W2, L3, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2.1, R2.2, R5, L3, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R2.1, R2.2, R5, R11, z11, L3, and L4 are as described herein, including in embodiments.
In embodiments, R2.1 is independently hydrogen, —OCX23, or unsubstituted 5 to 6 membered heteroaryl.
In embodiments, R2.2 is independently hydrogen or halogen.
In embodiments, R11 is independently halogen.
In embodiments, the compound has the formula:
R2, z2, R5, R6, L3, and L4 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R2, z2, R21, z21, R5, W1, W2, W3, L3, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R2, z2, R21, z21, R5, W1, W2, W3, L3, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R2, z2, R5, W1, W2, L3, and L4 are as described herein, including in embodiments.
In embodiments, W1 is independently —O—, —NH—, or —NR2—.
In embodiments, R2 is independently halogen, —OCX23, —OCH2X2, —OCHX22, unsubstituted C1-C3 alkyl, or unsubstituted 5 to 6 membered heteroaryl.
In embodiments, R21 is independently halogen, —OCX23, —OCH2X, —OCHX2, unsubstituted C1-C3 alkyl, or unsubstituted 5 to 6 membered heteroaryl.
In embodiments, L3 is —C(O)— or —CH2—.
In embodiments, L4 is —NH—, —NR4—, or —CH2—.
In embodiments, R16 is independently hydrogen, —C(O)N(CH3)2, or unsubstituted C1-C3 alkyl. In embodiments, R17 is independently hydrogen, —C(O)N(CH3)2, or unsubstituted C1-C3 alkyl. In embodiments, R18 is independently hydrogen, —C(O)N(CH3)2, or unsubstituted C1-C3 alkyl.
In embodiments, R5 is independently
wherein R16, R17, and R18 are independently hydrogen, —C(O)N(CH3)2, or unsubstituted C1-C3 alkyl.
In embodiments, the compound has the formula
or
R2.1, R2.2, R5, R21, z21, W1, W2, W3, L3, and L4 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R2.1, R2.2, R5, W1, W2, L3, and L4 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R5, R21, z21, W1, W2, W3, L3, and L4 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.2, R1.3, R1.4 , R1.5, R2, R3, R5, R21, L4, W1, W2, W3, z2 and z21 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2, R5, R21, L4, W1, W2, W3, z2 and z21 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2, R5, R21, L4, W1, W2, W3, z2 and z21 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2, R3, R5, R21, L4, W1, W2, W3, z2 and z21 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2, R3, R5, R21, L4, W1, W2, W3, z2 and z21 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2, R3, R5, R21, L4, W1, W2, W3, z2 and z21 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2, R3, R5, L4, W1, W2, and z2 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2, R5, L4, W1, W2, and z2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2, R5, L4, W1, W2, and z2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5 , R2, R3, R5, L4, W1, W2, and z2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2, R3, R5, L4, W1, W2, and z2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2, R3, R5, L4, W1, W2, and z2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2, R3, R5, L4, W1, W2, and z2 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, L4, W1, and W2 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.4, R1.5, R5, L4, W1, and W2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R5, L4, W1, and W2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, L4, W1, and W2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, L4, W1, and W2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, L4, W1, and W2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, L4, W1, and W2 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, L4, W1, and W2 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.4, R1.5, R5, L4, W1, and W2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R5, L4, W1, and W2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, L4, W1, and W2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, L4, W1, and W2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, L4, W1, and W2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, L4, W1, and W2 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2, R3, R5, L4, and z2 are as described herein, including in embodiments.
In embodiments, the compound has the formula
R1.2, R1.3, R1.4, R1.5, R2, R5, L4, and z2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2, R5, L4, and z2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2, R3, R5, L4, and z2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2, R3, R5, L4, and z2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2, R3, R5, L4, and z2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2, R3, R5, L4, and z2 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, and L4 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.4, R1.5, R5, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, and L4 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, and L4 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.4, R1.5, R5, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R5, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, and L4 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.4, R1.5, R2, R3, R5, R11, L4, z2, and z11 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.4, R1.5, R2, R5, R11, L4, z2, and z11 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R2, R5, R11, L4, z2, and z11 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R2, R3, R5, R11, L4, z2, and z11 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R2, R3, R5, R11, L4, z2, and z11 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R2, R3, R5, R11, L4, z2, and z11 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R2, R3, R5, R11, L4, z2, and z11 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, and L4 are as described herein, including in embodiments. R11.1 is independently hydrogen or any value of R11, as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.4, R1.5, R5, R11.1, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R5, R11.1, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5 , R3, R5, R11.1, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, R11.1, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, R11.1, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, R11.1, and L4 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, R11.1, and L4 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.4, R1.5, R5, R11.1, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R5, R11.1, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, R11.1, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, R11.1, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, R11.1, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, R11.1, and L4 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R21, L3, W1, W2, W3, and z21 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R21, L3, W1, W2, W3, and z21 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.2 , R1.3, R1.4, R1.5, R21, L3, W1, W2, W3, and z21 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R21, L3, W1, W2, W3, and z21 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R21, L3, W1, W2, 3, and z21 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2.1, R2.2, L3, W1, and W2 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2.1, R2.2, L3, W1, and W2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2.1, R2.2, L3, W1, and W2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2.1, R2.2, L3, W1, and W2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2.1, R2.2, L3, W1, and W2 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2.1, R2.2, and L3 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2.1, R2.2, and L3 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2.1, R2.2, and L3 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2.1, R2.2 , and L3 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2.1, R2.2, and L3 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.4, R1.5, R11, R2.1, R2.2, L3, and z11 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.4, R1.5, R11, R2.1, R2.2, L3, and z11 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R11, R2.1, R2.2, L3, and z11 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R11, R2.1, R2.2, L3, and z11 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R11, R2.1, R2.2, L3, and z11 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R2, R5, R11, L3, L4, and z11 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R2, R5, R11, L3, L4, z2, and z11 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R2, R5, L3, L4 and z2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R2, R5, L3, L4 and z2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R2, R5, L3, L4 and z2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R2, R5, R11, L3, L4, z2, and z11 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R5, R11, L3, L4, R2.1, R2.2, and z11 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R5, L3, L4, R2.1,and R2.2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R5, L3, L4, R2.1, and R2.2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R5, L3, L4, R2.1, and R2.2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R5, R11, L3, L4, R2.1, R2.2, and z11 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R5, R11, L3, L4 and z11 are as described herein, including in embodiments. R2.1 and R2.2 are independently hydrogen, —F, or —OCF3.
In embodiments, the compound has the formula:
R5, L3, and L4 are as described herein, including in embodiments. R2.1 and R2.2 are independently hydrogen, —F, or —OCF3. In embodiments, the compound has the formula:
R5, L3, and L4 are as described herein, including in embodiments. R2.1 and R2.2 are independently hydrogen, —F, or —OCF3. In embodiments, the compound has the formula:
R5, L3, and L4 are as described herein, including in embodiments. R2.1 and R2.2 are independently hydrogen, —F, or —OCF3. In embodiments, the compound has the formula:
R5, R11, L3, L4 and z11 are as described herein, including in embodiments. R2.1 and R2.2 are independently hydrogen, —F, or —OCF3.
In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2, R3, R16, R17, R18, L4, Ring B, and z2 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2, R16, R17, R18, L4, Ring B, and z2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
. R1.2, R1.3, R1.4, R1.5, R2, R16, R17, R18, L4, Ring B, and z2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
. R1.2, R1.3, R1.4, R1.5, R2, R3, R16. R17, R18, L4, Ring B, and z2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2, R3, R16, R17, R18, L4, Ring B, and z2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2, R3, R16, R17, R18, L4 Ring B, and z2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2, R3, R16, R17, R18, L4, Ring B, and z2 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2, R3, R5, L4, and z2 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2, R5, L4, and z2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2, R5, L4, and z2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2, R3, R5, L4, and z2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2, R3, R5, L4, and z2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2, R3, R5, L4, and z2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2, R3, R5, L4, and z2 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2, R3, R5, L4, and z2 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2, R5, L4, and z2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2, R5, L4, and z2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.2, R1.5, R1.4, R1.5, R2, R3, R5, L4, and z2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2, R3, R5, L4, and z2 are as described herein, including inembodiments. In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2, R3, R5, L4, and z2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2, R3, R5, L4, and z2 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, and L4 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.4, R1.5, R5, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R5, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, and L4 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, and L4 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.4, R1.5, R5, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R5, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5 , and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, and L4 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, and L4 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.4, R1.5, R5, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R5, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, and L4 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, and L4 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.4, R1.5, R5, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R5, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R3, R5, and L4 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
wherein R1, R2, R5, z1, z2, L3, L4, and Ring B are as described herein, including in embodiments.
In embodiments, the compound has the formula:
wherein R1.2, R1.3, R1.4, R1.5, R2, R5, z2, L3, L4, and Ring B are as described herein, including in embodiments.
In embodiments, the compound has the formula:
wherein R1.2, R1.3, R1.4, R1.5, R2, z2, R11, z11, R21, z21, R5, L3, L4, W1, W2, and W3 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R,2 z2, R21 , z21, R5, L3, L4, W1, W2, and W3 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2, z2, R5, L3, L4, W1, and W2 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.2, R1.3, R1.4, R1.5, R2, z2, R5, L3, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
R1.4, R1.5, R2, z2, R11, z11, R5, L3, and L4 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
wherein Ring B is phenyl, 5 to 6 membered heteroaryl, or 9 membered heteroaryl; and R2, z2, R5, L4, and L6 are as described herein, including in embodiments. In embodiments, the compound has the formula:
wherein Ring B is phenyl, 5 to 6 membered heteroaryl, or 9 membered heteroaryl; L4 is —NH— or —NR4—; R5 is
and R2, z2, R4, and L6 are as described herein, including in embodiments. In embodiments, the compound has the formula:
wherein Ring B is phenyl, 5 to 6 membered heteroaryl or 9 membered heteroaryl; L4 is —NH— or —NR4—; R5 is
and R2, z2, R4, and L6 are as described herein, including in embodiments.
In embodiments, the compound has the formula:
wherein W5 is CH, Ring B is phenyl; and R2, z1, R2, z2, z6, R5, L3, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
wherein W5 is CH, Ring B is phenyl; and R2, z2, R5, L3, and L4 are as described herein, including in embodiments. In embodiments, the compound has the formula:
wherein W5 is CH, Ring B is phenyl, L4 is —NH—; R5 is
and R2, z2, and L3 are as described herein, including in embodiments.
In embodiments, (Ring B)-(R2)z2 is
In embodiments, (Ring B)-(R2)z2 is
In embodiments, (Ring B)-(R2)z2 is
In embodiments, (Ring B)-(R2)z2
In embodiments, (Ring B)-(R2)z2
In embodiments, (Ring B)-(R2)z2
In embodiments, (Ring B)-(R2)z2
In embodiments, (Ring B)-(R2)z2
In embodiments, (Ring B)-(R2)z2
In embodiments, (Ring B)-(R2)z2
R1 is independently halogen, —CX13, —CHX12, —CH2X1, —OCX13, —OCH2X1, —OCHX12, —CN, —SOn1R1D, —SOv1NR1AR1B, —NR1CNR1AR1B, —ONR1AR1B, —NHC(O)NR1CNR1AR1B, —NHC(O)NR1AR1B, —N(O)m1, —NR1AR1B, —C(O)R1C, —C(O)—OR1C, —C(O) NR1AR1B, —OR1D, —NR1ASO2R1D, —NR1AC(O)R1C, —NR1AC(O)OR1C, —NR1AOR1C, —SF5, —N3, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl; two adjacent R1 substituents on adjacent carbons may optionally be joined to form a substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted phenyl, or substituted or unsubstituted heteroaryl or two R1 substituents bonded to the same carbon atom may optionally be joined to form a substituted or unsubstituted alkyl or substituted or unsubstituted heterocycloalkyl.
In embodiments, R1 is independently halogen, —CX13, —CHX12, —CH2X1, —OCX13, —OCH2X1, —OCHX12, —CN, —OH, —NH2, —COOH, —CONH2, —C(O)N(CH3)2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —SF5, —N3, substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted C6-C10 aryl, or substituted or unsubstituted 5 to 10 membered heteroaryl; two adjacent R1 substituents on adjacent carbons may optionally be joined to form a substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted phenyl, or substituted or unsubstituted 5 to 6 membered heteroaryl or two R1 substituents bonded to the same carbon atom may optionally be joined to form a substituted or unsubstituted C3-C6 cycloalkyl or substituted or unsubstituted 3 to 6 membered heterocycloalkyl.
In embodiments, R1 is independently halogen, —CCl3, —CBr3, —CF3, —CI3, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —OCI3, —N3, substituted or unsubstituted C1-C3 alkyl, substituted or unsubstituted 2 to 4 membered heteroalkyl, substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted phenyl, or substituted or unsubstituted 5 to 6 membered heteroaryl. In embodiments, R1 is independently halogen, —CCl3, —CBr3, —CF3, —CI3, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —OCI3, —N3, substituted or unsubstituted C1-C3 alkyl, or substituted or unsubstituted 2 to 4 membered heteroalkyl. In embodiments, R1 is independently halogen. In embodiments, R1 is independently —F. In embodiments, R1 is independently —Cl. In embodiments, R1 is independently-Br. In embodiments, R1 is independently —I. In embodiments, R1 is independently —CCl3. In embodiments, R1 is independently —CBr3. In embodiments, R1 is independently —CF3. In embodiments, R1 is independently —CI3. In embodiments, R1 is independently —CN. In embodiments, R1 is independently —OH. In embodiments, R1 is independently —NH2. In embodiments, R1 is independently —COOH. In embodiments, R1 is independently —CONH2. In embodiments, R1 is independently —OCCl3. In embodiments, R1 is independently —OCF3. In embodiments, R1 is independently —OCBr3. In embodiments, R1 is independently —OCI3. In embodiments, R1 is independently —N3. In embodiments, R1 is independently substituted or unsubstituted C1-C3 alkyl. In embodiments, R1 is independently unsubstituted methyl. In embodiments, R1 is independently unsubstituted ethyl. In embodiments, R1 is independently unsubstituted propyl. In embodiments, R1 is independently substituted or unsubstituted 2 to 4 membered heteroalkyl. In embodiments, R1 is independently unsubstituted 2 to 4 membered heteroalkyl. In embodiments, R1 is independently substituted or unsubstituted C3-C6 cycloalkyl. In embodiments, R1 is independently substituted or unsubstituted 3 to 6 membered heterocycloalkyl. In embodiments, R1 is independently substituted or unsubstituted phenyl. In embodiments, R1 is independently substituted or unsubstituted 5 to 6 membered heteroaryl. In embodiments, R1 is independently or substituted 5 to 6 membered heteroaryl. In embodiments, R1 is independently unsubstituted 5 to 6 membered heteroaryl. In embodiments, R1 is independently unsubstituted 5 membered heteroaryl. In embodiments, R1 is independently unsubstituted 6 membered heteroaryl.
In embodiments, two R1 substituents on adjacent carbons are joined to form a substituted or unsubstituted phenyl, or substituted or unsubstituted 5 to 6 membered heteroaryl. In embodiments, two R1 substituents on adjacent carbons are joined to form a substituted or unsubstituted phenyl. In embodiments, two R1 substituents on adjacent carbons are joined to form an R11-substituted phenyl. In embodiments, two R1 substituents on adjacent carbons are joined to form an unsubstituted phenyl. In embodiments, two R1 substituents on adjacent carbons are joined to form a substituted or unsubstituted 5 to 6 membered heteroaryl.
In embodiments, R2 is independently oxo, halogen, —CX23, —CHX22, —CH2X2, —OCX23, —OCH2X2, —OCHX22, —CN, —SOn2R2D, —SOv2NR2AR2B, —NR2CNR2AR2B, —ONR2AR2B, -NHC(O)NR2CNR2AR2B, —NHC(O)NR2AR2B, —N(O)m2, —NR2AR2B, —C(O)R2C, —C(O)—OR2C, —C(O) NR2AR2B, —OR2D, —NR2ASO2R2D, —NR2AC(O)R2C, —NR2AC(O)OR2C, —NR2AOR2C, —SF5, —N3, substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted C6-C10 aryl, or substituted or unsubstituted 5 to 10 membered heteroaryl; two adjacent R2 substituents on adjacent carbons may optionally be joined to form a substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted phenyl, or substituted or unsubstituted 5 to 6 membered heteroaryl.
In embodiments, R2 is independently halogen, —OCC13, —OCF3, —OCBr3, —OCI3, or unsubstituted 5 to 6 membered heteroaryl. In embodiments, R2 is independently halogen. In embodiments, R2 is independently —F. In embodiments, R2 is independently —Cl. In embodiments, R2 is independently —Br. In embodiments, R2 is independently —I. In embodiments, R2 is independently —OCC13. In embodiments, R2 is independently —OCF3. In embodiments, R2 is independently —OCBr3. In embodiments, R2 is independently —OCI3. In embodiments, R2 is unsubstituted 5 to 6 membered heteroaryl. In embodiments, R2 is unsubstituted 5 membered heteroaryl. In embodiments, R2 is unsubstituted 6 membered heteroaryl. In embodiments, R2 is unsubstituted pyrrolyl, pyrazolyl, pyridazinyl, triazinyl, pyrimidinyl, imidazolyl, pyrazinyl, oxazolyl, isoxazolyl, thiazolyl, furyl, thienyl, pyridyl, pyrimidyl, benzothiazolyl, benzoxazoyl, benzimidazolyl, benzofuran, isobenzofuranyl, indolyl, or isoindolyl. In embodiments, R2 is unsubstituted phenyl, benzimidazolyl, or indolyl. In embodiments, R2 is unsubstituted pyrrolyl. In embodiments, R2 is unsubstituted pyrazolyl. In embodiments, R2 is unsubstituted pyridazinyl. In embodiments, R2 is unsubstituted triazinyl. In embodiments, R2 is unsubstituted pyrimidinyl. In embodiments, R2 is unsubstituted imidazolyl. In embodiments, R2 is unsubstituted pyrazinyl. In embodiments, R2 is unsubstituted oxazolyl. In embodiments, R2 is unsubstituted isoxazolyl. In embodiments, R2 is unsubstituted thiazolyl. In embodiments, R2 is unsubstituted furyl. In embodiments, R2 is unsubstituted thienyl. In embodiments, R2 is unsubstituted pyridyl. In embodiments, R2 is unsubstituted pyrimidyl. In embodiments, R2 is unsubstituted benzothiazolyl. In embodiments, R2 is unsubstituted benzoxazoyl. In embodiments, R2 is unsubstituted benzimidazolyl. In embodiments, R2 is unsubstituted benzofuran. In embodiments, R2 is unsubstituted isobenzofuranyl. In embodiments, R2 is unsubstituted indolyl. In embodiments, R2 is or unsubstituted isoindolyl. In embodiments, R2 is independently —F or —OCF3.
In embodiments, R2 is independently halogen, —OCC13, —OCF3, —OCBr3, —OCI3, or substituted 5 to 6 membered heteroaryl. In embodiments, R2 is independently halogen. In embodiments, R2 is independently —F. In embodiments, R2 is independently —Cl. In embodiments, R2 is independently —Br. In embodiments, R2 is independently —I. In embodiments, R2 is independently —OCC13. In embodiments, R2 is independently —OCF3. In embodiments, R2 is independently —OCBr3. In embodiments, R2 is independently —OCI3. In embodiments, R2 is substituted 5 to 6 membered heteroaryl. In embodiments, R2 is substituted 5 membered heteroaryl. In embodiments, R2 is substituted 6 membered heteroaryl. In embodiments, R2 is substituted pyrrolyl, pyrazolyl, pyridazinyl, triazinyl, pyrimidinyl, imidazolyl, pyrazinyl, oxazolyl, isoxazolyl, thiazolyl, furyl, thienyl, pyridyl, pyrimidyl, benzothiazolyl, benzoxazoyl, benzimidazolyl, benzofuran, isobenzofuranyl, indolyl, or isoindolyl. In embodiments, R2 is substituted phenyl, benzimidazolyl, or indolyl. In embodiments, R2 is substituted pyrrolyl. In embodiments, R2 is substituted pyrazolyl. In embodiments, R2 is substituted pyridazinyl. In embodiments, R2 is substituted triazinyl. In embodiments, R2 is substituted pyrimidinyl. In embodiments, R2 is substituted imidazolyl. In embodiments, R2 is substituted pyrazinyl. In embodiments, R2 is substituted oxazolyl. In embodiments, R2 is substituted isoxazolyl. In embodiments, R2 is substituted thiazolyl. In embodiments, R2 is substituted furyl. In embodiments, R2 is substituted thienyl. In embodiments, R2 is substituted pyridyl. In embodiments, R2 is substituted pyrimidyl. In embodiments, R2 is substituted benzothiazolyl. In embodiments, R2 is substituted benzoxazoyl. In embodiments, R2 is substituted benzimidazolyl. In embodiments, R2 is substituted benzofuran. In embodiments, R2 is substituted isobenzofuranyl. In embodiments, R2 is substituted indolyl. In embodiments, R2 is or substituted isoindolyl. In embodiments, R2 is independently —F or —OCF3.
In embodiments, L3 is a bond, —S(O)2—, —NR3—, —NH—, —O—, —S—, —C(O)—, —C(O)NR3—, —NR3C(O)—, —N(R3)CH2—, —NR3C(O)NH —, —NHC(O)NR3—, —C(O)O—, —OC(O)—, substituted or unsubstituted C1-C6 alkylene, or substituted or unsubstituted 2 to 6 membered heteroalkylene.
In embodiments, L3 is —C(O)—, —CH2—, —C(O)NR3—, —CH2CH2NR3—, —C(O)CH2NR3—, or —CH2C(O)NR3. In embodiments, L3 is —C(O)—. In embodiments, L3 is —CH2—. In embodiments, L3 is —C(O)NR3—. In embodiments, L3 is —CH2CH2NR3—. In embodiments, L3 is —C(O)CH2NR3—. In embodiments, L3 is —CH2C(O)NR3. In embodiments, L3 is —C(O)—, —CH2—, —C(O)NH—, —CH2CH2NH—, —C(O)CH2NH—, or —CH2C(O)NH. In embodiments, wherein L3 is —CH2— or —C(O)NH—. In embodiments, L3 is —C(O)NH—. In embodiments, L3 is —CH2CH2NH—. In embodiments, L3 is —C(O)CH2NH—. In embodiments, L3 is or —CH2C(O)NH. In embodiments, L3 is a bond, substituted or unsubstituted C1-C6 alkylene, or substituted or unsubstituted 2 to 6 membered heteroalkylene. In embodiments, L3 is a bond. In embodiments, L3 is substituted or unsubstituted C1-C6 alkylene. In embodiments, L3 is substituted or unsubstituted 2 to 6 membered heteroalkylene.
In embodiments, L4 is —NH—.
In embodiments, L4 is —CH2—.
In embodiments, L4 is —N(CH3)—.
In embodiments, L6 is —N(R6)—L3—. In embodiments, L6 is —N(R6)—L3—; L3 is —CH2—; and R6 is as described herein, including embodiments.
In embodiments, L6 is —N(R6)—L3—; L3 is —CH2—; and R6 is —CF3, —COCH3, or cyclopropyl.
In embodiments, L6 is —C(O)NH—.
In embodiments, W5 is CH. In embodiments, W5 is N.
In embodiments, R3, R4, and R6 are independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHC12, —CHBr2, —CHF2, —CHI2, —CH2CI, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CO(C1-C6 alkyl), —CONH2, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHC12, —OCHBr2, —OCHI2, —OCHF2, —OCH2 C1, —OCH2Br, —OCH2I, —OCH2F, unsubstituted C1-C6 alkyl, unsubstituted 2 to 6 membered heteroalkyl, unsubstituted C3-C6 cycloalkyl,or unsubstituted 3 to 6 membered heterocycloalkyl.
In embodiments, R3, R4, and R6 are independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHC12, —CHBr2, —CHF2, —CHI2, —CH2C1, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHC12, —OCHBr2, —OCHI2, —OCHF2, —OCH2C1, —OCH2Br, —OCH2I, —OCH2F, unsubstituted C1-C6 alkyl, or unsubstituted 2 to 6 membered heteroalkyl.
In embodiments, R3 is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHC12, —CHBr2, —CHF2, —CHI2, —CH2C1, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —COCH3, —CONH2, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHC12, —OCHBr2, —OCHI2, —OCHF2, —OC H2Cl, —OCH2Br, —OCH2I, —OCH2F, unsubstituted C1-C6 alkyl, unsubstituted 2 to 6 membered heteroalkyl, unsubstituted C3-C6 cycloalkylene, or unsubstituted 3 to 6 membered heterocycloalkylene.
In embodiments, R3 is independently hydrogen, —CC13, —CBr3, —CF3, —CI3, CHC12, —CHBr2, —CHF2, —CHI2, —CH2C1, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHC12, —OCHBr2, —OCHI2, —OCHF2, —OCH2C1, —OCH2Br, —OCH2I, —OCH2F, unsubstituted C1-C6 alkyl, or unsubstituted 2 to 6 membered heteroalkyl.
In embodiments, R4 is independently hydrogen, —CC13, —CBr3, —CF3, —CI3, CHC12, —CHBr2, —CHF2, —CHI2, —CH2C1, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —COCH3, —CONH2, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHC12, —OCHBr2, —OCHI2, —OCHF2, —OC H2Cl, —OCH2Br, —OCH2I, —OCH2F, unsubstituted C1-C6 alkyl, unsubstituted 2 to 6 membered heteroalkyl, unsubstituted C3-C6 cycloalkylene, or unsubstituted 3 to 6 membered heterocycloalkylene.
In embodiments, R4 is independently hydrogen, —CC13, —CBr3, —CF3, —CI3, CHC12, —CHBr2, —CHF2, —CHI2, —CH2C1, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHC12, —OCHBr2, —OCHI2, —OCHF2, —OCH2C1, —OCH2Br, —OCH2I, —OCH2F, unsubstituted C1-C6 alkyl, or unsubstituted 2 to 6 membered heteroalkyl.
In embodiments, R6 is independently hydrogen, —CC13, —CBr3, —CF3, —CI3, CHC12, —CHBr2, —CHF2, —CHI2, —CH2C1, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —COCH3, —CONH2, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHC12, —OCHBr2, —OCHI2, —OCHF2, —OC H2Cl, —OCH2Br, —OCH2I, —OCH2F, unsubstituted C1-C6 alkyl, unsubstituted 2 to 6 membered heteroalkyl, unsubstituted C3-C6 cycloalkylene, or unsubstituted 3 to 6 membered heterocycloalkylene.
In embodiments, R6 is independently hydrogen, —CC13, —CBr3, —CF3, —CI3, CHC12, —CHBr2, —CHF2, —CHI2, —CH2C1, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHC12, —OCHBr2, —OCHI2, —OCHF2, —OCH2C1, —OCH2Br, —OCH2I, —OCH2F, unsubstituted C1-C6 alkyl, or unsubstituted 2 to 6 membered heteroalkyl.
In embodiments, R3 is independently hydrogen. In embodiments, R3 is independently —CC13. In embodiments, R3 is independently —CBr3. In embodiments, R3 is independently —CF3. In embodiments, R3 is independently —CI3. In embodiments, R3 is independently CHCl2. In embodiments, R3 is independently —CHBr2. In embodiments, R3 is independently —CHF2. In embodiments, R3 is independently —CHI2. In embodiments, R3 is independently —C(O)CH3. In embodiments, R3 is independently —CH2Cl. In embodiments, R3 is independently —CH2Br. In embodiments, R3 is independently —CH2F. In embodiments, R3 is independently —CH2I. In embodiments, R3 is independently unsubstituted C1-C6 alkyl. In embodiments, R3 is independently unsubstituted C1-C2 alkyl. In embodiments, R3 is independently unsubstituted methyl. In embodiments, R3 is independently unsubstituted 2 to 6 membered heteroalkyl. In embodiments, R3 is independently unsubstituted C3-C6 cycloalkyl. In embodiments, R3 is independently unsubstituted cyclopropyl. In embodiments, R3 is independently unsubstituted cyclobutyl. In embodiments, R3 is independently unsubstituted cyclopentyl. In embodiments, R3 is independently unsubstituted cyclohexyl. In embodiments, R3 is independently unsubstituted 3 to 6 membered heterocycloalkyl.
In embodiments, R4 is independently hydrogen. In embodiments, R4 is independently —CCl3. In embodiments, R4 is independently —CBr3. In embodiments, R4 is independently —CF3. In embodiments, R4 is independently —CI3. In embodiments, R4 is independently CHCl2. In embodiments, R4 is independently —CHBr2. In embodiments, R4 is independently —CHF2. In embodiments, R4 is independently —CHI2. In embodiments, R4 is independently —CH2Cl. In embodiments, R4 is independently —CH2Br. In embodiments, R4 is independently —CH2F. In embodiments, R4 is independently —CH2I. In embodiments, R4 is independently —C(O)CH3. In embodiments, R4 is independently unsubstituted C1-C6 alkyl. In embodiments, R4 is independently unsubstituted C1-C2 alkyl. In embodiments, R4 is independently unsubstituted methyl. In embodiments, R4 is independently unsubstituted 2 to 6 membered heteroalkyl. In embodiments, R4 is independently unsubstituted C3-C6 cycloalkyl. In embodiments, R4 is independently unsubstituted cyclopropyl. In embodiments, R4 is independently unsubstituted cyclobutyl. In embodiments, R4 is independently unsubstituted cyclopentyl. In embodiments, R4 is independently unsubstituted cyclohexyl. In embodiments, R4 is independently unsubstituted 3 to 6 membered heterocycloalkyl.
In embodiments, R6 is independently hydrogen. In embodiments, R6 is independently —CCl3. In embodiments, R6 is independently —CBr3. In embodiments, R6 is independently —CF3. In embodiments, R6 is independently —CI3. In embodiments, R6 is independently CHCl2. In embodiments, R6 is independently —CHBr2. In embodiments, R6 is independently —CHF2. In embodiments, R6 is independently —CHI2. In embodiments, R6 is independently —CH2Cl. In embodiments, R6 is independently —CH2Br. In embodiments, R6 is independently —CH2F. In embodiments, R6 is independently —CH2I. In embodiments, R6 is independently —C(O)CH3. In embodiments, R6 is independently unsubstituted C1-C6 alkyl. In embodiments, R6 is independently unsubstituted C1-C2 alkyl. In embodiments, R6 is independently unsubstituted methyl. In embodiments, R6 is independently unsubstituted 2 to 6 membered heteroalkyl. In embodiments, R6 unsubstituted C3-C6 cycloalkyl. In embodiments, R6 is independently unsubstituted cyclopropyl. In embodiments, R6 is independently unsubstituted cyclobutyl. In embodiments, R6 is independently unsubstituted cyclopentyl. In embodiments, R6 is independently unsubstituted cyclohexyl. In embodiments, R6 is independently unsubstituted 3 to 6 membered heterocycloalkyl.
In embodiments, R7 is independently hydrogen or unsubstituted C1-C10 alkyl. In embodiments, R7 is independently hydrogen or unsubstituted C1-C6 alkyl. In embodiments, R7 is independently hydrogen or unsubstituted C1-C4 alkyl. In embodiments, R7 is independently hydrogen or unsubstituted methyl. In embodiments, R7 is independently hydrogen or unsubstituted ethyl. In embodiments, R7 is independently hydrogen. In embodiments, R7 is independently unsubstituted methyl. In embodiments, R7 is independently unsubstituted ethyl.
In embodiments, R8 is independently hydrogen or unsubstituted C1-C10 alkyl. In embodiments, R8 is independently hydrogen or unsubstituted C1-C6 alkyl. In embodiments, R8 is independently hydrogen or unsubstituted C1-C4 alkyl. In embodiments, R8 is independently hydrogen or unsubstituted methyl. In embodiments, R8 is independently hydrogen or unsubstituted ethyl. In embodiments, R8 is independently hydrogen. In embodiments, R8 is independently unsubstituted methyl. In embodiments, R8 is independently unsubstituted ethyl.
In embodiments, R9 is independently hydrogen or unsubstituted C1-C10 alkyl. In embodiments, R9 is independently hydrogen or unsubstituted C1-C6 alkyl. In embodiments, R9 is independently hydrogen or unsubstituted C1-C4 alkyl. In embodiments, R9 is independently hydrogen or unsubstituted methyl. In embodiments, R9 is independently hydrogen or unsubstituted ethyl. In embodiments, R9 is independently hydrogen. In embodiments, R9 is independently unsubstituted methyl. In embodiments, R9 is independently unsubstituted ethyl.
In embodiments, R10 is independently hydrogen or unsubstituted C1-C10 alkyl. In embodiments, R10 is independently hydrogen or unsubstituted C1-C6 alkyl. In embodiments, R10 is independently hydrogen or unsubstituted C1-C4 alkyl. In embodiments, R10 is independently hydrogen or unsubstituted methyl. In embodiments, R10 is independently hydrogen or unsubstituted ethyl. In embodiments, R10 is independently hydrogen. In embodiments, R10 is independently unsubstituted methyl. In embodiments, R10 is independently unsubstituted ethyl.
In embodiments, R7 and R8 are hydrogen. In embodiments, R7 and R8 are unsubstituted C1-C6 alkyl. In embodiments, R7 and R8 are unsubstituted methyl. In embodiments, R9 and R10 are hydrogen. In embodiments, R9 and R10 are unsubstituted C1-C6 alkyl. In embodiments, R9 and R10 are unsubstituted methyl. In embodiments, R7 and R8 are hydrogen and R9 and R10 are unsubstituted C1-C6 alkyl. In embodiments, R7 and R8 are hydrogen and R9 and R10 are unsubstituted methyl. In embodiments, R9 and R10 are hydrogen and R7 and R8 are unsubstituted C1-C6 alkyl. In embodiments, R9 and R10 are hydrogen and R7 and R8 are unsubstituted methyl.
In embodiments, Ring B is aryl. In embodiments, Ring B is C6-C10 aryl. In embodiments, Ring B is phenyl. In embodiments, Ring B is C9 aryl. In embodiments, Ring B is C10 aryl. In embodiments, Ring B is heteroaryl. In embodiments, Ring B is 5 to 10 membered heteroaryl. In embodiments, Ring B is 5 to 6 membered heteroaryl. In embodiments, Ring B is 9 to 10 membered heteroaryl. In embodiments, Ring B is 5-membered heteroaryl. In embodiments, Ring B is 6-membered heteroaryl. In embodiments, Ring B is pyrrolyl, pyrazolyl, pyridazinyl, triazinyl, pyrimidinyl, imidazolyl, pyrazinyl, oxazolyl, isoxazolyl, thiazolyl, furyl, thienyl, pyridyl, pyrimidyl, benzothiazolyl, benzoxazoyl, benzimidazolyl, benzofuran, isobenzofuranyl, indolyl, or isoindolyl. In embodiments, Ring B is phenyl, benzimidazolyl, or indolyl. In embodiments, Ring B is pyrrolyl. In embodiments, Ring B is pyrazolyl. In embodiments, Ring B is pyridazinyl. In embodiments, Ring B is triazinyl. In embodiments, Ring B is pyrimidinyl. In embodiments, Ring B is imidazolyl. In embodiments, Ring B is pyrazinyl. In embodiments, Ring B is oxazolyl. In embodiments, Ring B is isoxazolyl. In embodiments, Ring B is thiazolyl. In embodiments, Ring B is furyl. In embodiments, Ring B is thienyl. In embodiments, Ring B is pyridyl. In embodiments, Ring B is pyrimidyl. In embodiments, Ring B is benzothiazolyl. In embodiments, Ring B is benzoxazoyl. In embodiments, Ring B is benzimidazolyl. In embodiments, Ring B is benzofuran. In embodiments, Ring B is isobenzofuranyl. In embodiments, Ring B is indolyl. In embodiments, Ring B is isoindolyl.
In embodiments, -(Ring B)-(R2)z2 is R2-substituted or unsubstituted C6-C10 aryl. In embodiments, Ring B is R2-substituted or unsubstituted phenyl. In embodiments, Ring B is R2-substituted or unsubstituted C9 aryl. In embodiments, Ring B is R2-substituted or unsubstituted C10 aryl. In embodiments, Ring B is R2-substituted or unsubstituted 5 to 10 membered heteroaryl. In embodiments, Ring B is R2-substituted or unsubstituted 5 to 6 membered heteroaryl. In embodiments, Ring B is R2-substituted or unsubstituted 9 to 10 membered heteroaryl. In embodiments, Ring B is R2-substituted or unsubstituted 5-membered heteroaryl. In embodiments, Ring B is R2-substituted or unsubstituted 6-membered heteroaryl. In embodiments, Ring B is R2-substituted or unsubstituted pyrrolyl, pyrazolyl, pyridazinyl, triazinyl, pyrimidinyl, imidazolyl, pyrazinyl, oxazolyl, isoxazolyl, thiazolyl, furyl, thienyl, pyridyl, pyrimidyl, benzothiazolyl, benzoxazoyl, benzimidazolyl, benzofuran, isobenzofuranyl, indolyl, or isoindolyl. In embodiments, Ring B is R2-substituted or unsubstituted phenyl, benzimidazolyl, or indolyl. In embodiments, Ring B is R2-substituted or unsubstituted pyrrolyl. In embodiments, Ring B is R2-substituted or unsubstituted pyrazolyl. In embodiments, Ring B is R2-substituted or unsubstituted pyridazinyl. In embodiments, Ring B is R2-substituted or unsubstituted triazinyl. In embodiments, Ring B is R2-substituted or unsubstituted pyrimidinyl. In embodiments, Ring B is R2-substituted or unsubstituted imidazolyl. In embodiments, Ring B is R2-substituted or unsubstituted pyrazinyl. In embodiments, Ring B is R2-substituted or unsubstituted oxazolyl. In embodiments, Ring B is R2-substituted or unsubstituted isoxazolyl. In embodiments, Ring B is R2-substituted or unsubstituted thiazolyl. In embodiments, Ring B is R2-substituted or unsubstituted furyl. In embodiments, Ring B is R2-substituted or unsubstituted thienyl. In embodiments, Ring B is R2-substituted or unsubstituted pyridyl. In embodiments, Ring B is R2-substituted or unsubstituted pyrimidyl. In embodiments, Ring B is R2-substituted or unsubstituted benzothiazolyl. In embodiments, Ring B is R2-substituted or unsubstituted benzoxazoyl. In embodiments, Ring B is R2-substituted or unsubstituted benzimidazolyl. In embodiments, Ring B is R2-substituted or unsubstituted benzofuran. In embodiments, Ring B is R2-substituted or unsubstituted isobenzofuranyl. In embodiments, Ring B is R2-substituted or unsubstituted indolyl. In embodiments, Ring B is R2-substituted or unsubstituted isoindolyl.
In embodiments, Ring B has the formula:
R2.1 and R2.2 are as described herein, including in embodiments.
In embodiments, Ring B has the formula:
R2.1 is as described herein, including in embodiments. In embodiments, Ring B has the formula:
R2.1 and R2.2 are as described herein, including in embodiments. In embodiments, Ring B has the formula:
R2.1 is as described herein, including in embodiments. In embodiments, Ring B has the formula:
R2.1 and R2.2 are as described herein, including in embodiments. In embodiments, Ring B has the formula:
R2.1 is as described herein, including in embodiments. In embodiments, Ring B has the formula:
R2.1 and R2.2 are as described herein, including in embodiments.
In embodiments, Ring B has the formula:
R2, z2, W1, W2, and W3 are as described herein, including in embodiments.
In embodiments, R5 is independently
R16, R17, and R18 are as described herein, including in embodiments. In embodiments, R5 is independently
R17 is as described herein, including in embodiments. In embodiments, R5 is independently
R17 is as described herein, including in embodiments. In embodiments, R5 is independently
R17 is as described herein, including in embodiments. In embodiments, R5 is independently
R17 is as described herein, including in embodiments. In embodiments, R5 is independently
R16, R17, and R18 are as described herein, including in embodiments. In embodiments, R5 is independently
R16, R17, and R18 are as described herein, including in embodiments. In embodiments, R5 is independently
R16, R17, and R18 are as described herein, including in embodiments. In embodiments, R5 is independently
R16, R17, R18, and R19 are as described herein, including in embodiments. In embodiments, R5 is independently
R16, R17, R18, R19, and R20 are as described herein, including in embodiments. In embodiments, R5 is independently
R15, R16, R17, and R18 are as described herein, including in embodiments. In embodiments, R5 is independently
R14, R16, R17, and R18 are as described herein, including in embodiments. In embodiments, R5 is independently
R16, R17, and R18 are as described herein, including in embodiments. In embodiments, R5 is independently
R14, R15, R16, R17, and R18 are as described herein, including in embodiments.
In embodiments, R5 is independently
R17 is substituted or unsubstituted alkyl. In embodiments, R17 is unsubstituted alkyl. In embodiments, R17 is unsubstituted methyl. In embodiments, R17 is unsubstituted ethyl. In embodiments, R17 is unsubstituted propyl.
In embodiments, R5 is independently
R16, R17, and R18 are as described herein, including in embodiments. R19 is hydrogen, —CF3, —CN, or unsubstituted methyl. In embodiments, R19 is hydrogen. In embodiments, R19 is —CF3. In embodiments, R19 is —CN. In embodiments, R19 is unsubstituted methyl. In embodiments, R16, R17, and R18 are hydrogen.
In embodiments, R5 is independently
R16, R17, and R18 are as described herein, including in embodiments. R19 and R20 are independently hydrogen, —CF3, —CN, or unsubstituted methyl. In embodiments, R19 is hydrogen. In embodiments, R19 is —CF3. In embodiments, R19 is —CN. In embodiments, R19 is unsubstituted methyl. In embodiments, R20 is hydrogen. In embodiments, R20 is —CF3. In embodiments, R20 is —CN. In embodiments, R20 is unsubstituted methyl. In embodiments, R16, R17, and R18 are hydrogen.
In embodiments, R5 is independently
R15, R16, R17, and R18 are as described herein, including in embodiments. In embodiments, R17 is substituted or unsubstituted phenyl. In embodiments, R5 is independently
R14, R16, R17, and R18 are as described herein, including in embodiments. In embodiments, R17 is substituted or unsubstituted phenyl. In embodiments, R5 is independently
R16, R17, and R18 are as described herein, including in embodiments. In embodiments, R17 is substituted or unsubstituted phenyl. In embodiments, R5 is independently
R14, R15, R16, R17, and R18 are as described herein, including in embodiments. In embodiments, R17 is substituted or unsubstituted phenyl.
In embodiments, R14 is independently ═O. In embodiments, R14 is independently ═NR19.
In embodiments, R15 is independently ═O. In embodiments, R15 is independently ═NR20.
In embodiments, R5 is independently
R16 and R17 are as described herein, including in embodiments.
In embodiments, R5 is independently
R17 is as described herein, including in embodiments.
In embodiments, R5 is independently
R17 is as described herein, including in embodiments. In embodiments, R17 is substituted or unsubstituted heteroaryl. In embodiments, R17 is substituted or unsubstituted 5 to 6 membered heteroaryl. In embodiments, R17 is substituted or unsubstituted pyrrolyl, pyrazolyl, pyridazinyl, triazinyl, pyrimidinyl, imidazolyl, pyrazinyl, oxazolyl, isoxazolyl, thiazolyl, furyl, thienyl, pyridyl, or pyrimidyl. In embodiments, R17 is substituted or unsubstituted triazinyl. In embodiments, R17 is unsubstituted triazinyl. In embodiments, R17 is substituted or unsubstituted benzothiazolyl, benzoxazoyl, benzimidazolyl, benzofuran, isobenzofuranyl, indolyl, isoindolyl, benzothiophenyl, isoquinolyl, quinoxalinyl, or quinolyl.
In embodiments, R5 is independently
R16 is as described herein, including in embodiments. In embodiments, R16 is substituted or unsubstituted heteroaryl. In embodiments, R16 is substituted or unsubstituted 5 to 6 membered heteroaryl. In embodiments, R16 is substituted or unsubstituted pyrrolyl, pyrazolyl, pyridazinyl, triazinyl, pyrimidinyl, imidazolyl, pyrazinyl, oxazolyl, isoxazolyl, thiazolyl, furyl, thienyl, pyridyl, or pyrimidyl. In embodiments, R16 is substituted or unsubstituted triazinyl. In embodiments, R16 is unsubstituted triazinyl. In embodiments, R16 is substituted or unsubstituted benzothiazolyl, benzoxazoyl, benzimidazolyl, benzofuran, isobenzofuranyl, indolyl, isoindolyl, benzothiophenyl, isoquinolyl, quinoxalinyl, or quinolyl.
In embodiments, R5 is independently
R17 is as described herein, including in embodiments. In embodiments, R5 is independently
R17 is as described herein, including in embodiments. In embodiments, R5 is independently
R17 is as described herein, including in embodiments. In embodiments, R5 is independently
R17 is as described herein, including in embodiments. In embodiments, R5 is independently
R17 is as described herein, including in embodiments. In embodiments, R5 is independently
R17 is as described herein, including in embodiments. In embodiments, R5 is independently
R17 is as described herein, including in embodiments. In embodiments, R5 is independently embodiments.
R17 is as described herein, including in
In embodiments, R5 is independently
In embodiments, R17 is substituted or unsubstituted aryl. In embodiments, R17 is substituted or unsubstituted phenyl. In embodiments, R17 is unsubstituted phenyl. In embodiments, R5 is independently
In embodiments, R17 is substituted or unsubstituted aryl. In embodiments, R17 is substituted or unsubstituted phenyl. In embodiments, R17 is unsubstituted phenyl. In embodiments, R5 is independently
In embodiments, R17 is substituted or unsubstituted aryl. In embodiments, R17 is substituted or unsubstituted phenyl. In embodiments, R17 is unsubstituted phenyl. In embodiments, R5 is independently
In embodiments, R17 is substituted or unsubstituted aryl. In embodiments, R17 is substituted or unsubstituted phenyl. In embodiments, R17 is unsubstituted phenyl. In embodiments, R5 is independently
In embodiments, R17 is substituted or unsubstituted aryl. In embodiments, R17 is substituted or unsubstituted phenyl. In embodiments, R17 is unsubstituted phenyl. In embodiments, R5 is independently
In embodiments, R17 is substituted or unsubstituted aryl. In embodiments, R17 is substituted or unsubstituted phenyl. In embodiments, R17 is unsubstituted phenyl. In embodiments, R5 is independently
In embodiments, R17 is substituted or unsubstituted aryl. In embodiments, R17 is substituted or unsubstituted phenyl. In embodiments, R17 is unsubstituted phenyl. In embodiments, R5 is independently
In embodiments, R17 is substituted or unsubstituted aryl. In embodiments, R17 is substituted or unsubstituted phenyl. In embodiments, R17 is unsubstituted phenyl.
In embodiments, R5 is independently:
In embodiments, R5 is independently:
In embodiments, R5 is independently
In embodiments, R5 is independently
In embodiments, R5 is independently
In embodiments, R5 is independently
In embodiments, R5 is independently
In embodiments, R5 is independently
In embodiments, R5 is independently
In embodiments, R5 is independently
In embodiments, R5 is independently
In embodiments, R5 is independently
In embodiments, R5 is independently
In embodiments, R5 is independently
In embodiments, R5 is independently
In embodiments, R5 is independently
In embodiments, R5 is independently
In embodiments, R5 is independently
In embodiments, R5 is independently
In embodiments, L4-R5 is independently
R16, R17, R18, and R19 are as described herein, including in embodiments. R16, R17, and R18 are as described herein, including in embodiments. R19 is hydrogen, —CF3, —CN, or unsubstituted methyl. In embodiments, R19 is hydrogen. In embodiments, R19 is —CF3. In embodiments, R19 is —CN. In embodiments, R19 is unsubstituted methyl. In embodiments, R16, R17, and R18 are hydrogen.
In embodiments, L4-R5 is independently
R16, R17, R18, and R19 are as described herein, including in embodiments. R16, R17, and R18 are as described herein, including in embodiments. R19 is hydrogen, —CF3, —CN, or unsubstituted methyl. In embodiments, R19 is hydrogen. In embodiments, R19 is —CF3. In embodiments, R19 is —CN. In embodiments, R19 is unsubstituted methyl. In embodiments, R16, R17, and R18 are hydrogen.
In embodiments, L4-R5 is independently
R16, R17, and R18 are as described herein, including in embodiments. R19 and R20 are independently hydrogen, —CF3, —CN, or unsubstituted methyl. In embodiments, R19 and R20 are independently hydrogen or unsubstituted methyl. In embodiments, R19 is hydrogen. In embodiments, R19 is unsubstituted methyl. In embodiments, R20 is hydrogen. In embodiments, R20 is unsubstituted methyl. In embodiments, R16, R17, and R18 are hydrogen.
In embodiments, L4-R5 is independently
R15, R16, R17, and R18 are as described herein, including in embodiments. In embodiments, R17 is substituted or unsubstituted phenyl. In embodiments, L4-R5 is independently
R14, R16, R17, and R18 are as described herein, including in embodiments. In embodiments, R17 is substituted or unsubstituted phenyl. In embodiments, L4-R5 is independently
R16, R17, and R18 are as described herein, including in embodiments. In embodiments, R17 is substituted or unsubstituted phenyl. In embodiments, L4-R5 is independently
R14, R15, R16, R17, and R18 are as described herein, including in embodiments. In embodiments, R17 is substituted or unsubstituted phenyl.
In embodiments, L4-R5 is independently
R15 is as described herein, including in embodiments; R17 is substituted or unsubstituted phenyl; and R16 and R18 are hydrogen. In embodiments, L4-R5 is independently
R15 is as described herein, including in embodiments; R17 is substituted or unsubstituted phenyl; and R16 and R18 are hydrogen. In embodiments, L4-R5 is independently
R15 is as described herein, including in embodiments; R17 is substituted or unsubstituted phenyl; and R16 and R18 are hydrogen. In embodiments, L4-R5 is independently
R15 is as described herein, including in embodiments; R17 is substituted or unsubstituted phenyl; and R16 and R18 are hydrogen.
In embodiments, L4-R5 is independently
In embodiments, L4-R5 is independently
In embodiments, L4-R5 is independently
In embodiments, L4-R5 is independently
In embodiments, L4-R5 is independently
In embodiments, L4-R5 is independently
In embodiments, L4-R5 is independently
In embodiments, L4-R5 is independently
In embodiments, L4-R5 is independently
In embodiments, R16, R17, and R18 are independently hydrogen, oxo, halogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —C(O)N(CH3)2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, —N3, substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted C6-C12 aryl, or substituted or unsubstituted 5 to 12 membered heteroaryl.
In embodiments, R16, R17, and R18 are independently hydrogen, substituted or unsubstituted C1-C6 alkyl, or substituted or unsubstituted 2 to 6 membered heteroalkyl. In embodiments, R16, R17, and R18 are independently hydrogen. In embodiments, R16, R17, and R18 are independently substituted or unsubstituted C1-C6 alkyl. In embodiments, R16, R17, and R18 are independently substituted or unsubstituted 2 to 6 membered heteroalkyl. In embodiments, R16, R17, and R18 are independently substituted or unsubstituted 2 to 3 membered heteroalkyl. In embodiments, R16, R17, and R18 are independently hydrogen or —C(O)N(CH3)2. In embodiments, R16, R17, and R18 are independently hydrogen or substituted or unsubstituted C1-C6 alkyl. In embodiments, R16, R17, and R18 are independently hydrogen or substituted or unsubstituted C1-C4 alkyl. In embodiments, R16, R17, and R18 are independently hydrogen or substituted or unsubstituted C1-C2 alkyl. In embodiments, R16, R17, and R18 are independently hydrogen or unsubstituted methyl. In embodiments, R16 and R17 are hydrogen and R18 is unsubstituted methyl. In embodiments, R16 and R18 are hydrogen and R17 is —C(O)N(CH3)2. In embodiments, R16, R17, and R18 are hydrogen. In embodiments, R17 is hydrogen or substituted or unsubstituted C1-C4 alkyl. In embodiments, R17 is hydrogen. In embodiments, R17 is unsubstituted methyl. In embodiments, R17 is ethyl. In embodiments, R17 is propyl. In embodiments, R17 is isopropyl. In embodiments, R17 is n-propyl.
In embodiments, R16 and R18 are hydrogen and R17 is substituted or unsubstituted aryl. In embodiments, R16 and R18 are hydrogen and R17 is unsubstituted C6-C12 aryl. In embodiments, R16 and R18 are hydrogen and R17 is substituted or unsubstituted phenyl. In embodiments, R16 and R18 are hydrogen and R17 is unsubstituted phenyl.
In embodiments, R16 and R18 are hydrogen and R17 is substituted or unsubstituted 5 to 6 membered heteroaryl. In embodiments, R16 and R18 are hydrogen and R17 is unsubstituted 5 to 6 membered heteroaryl. In embodiments, R16 and R18 are hydrogen and R17 is substituted or unsubstituted pyrrolyl. In embodiments, R16 and R18 are hydrogen and R17 is substituted or unsubstituted pyrazolyl. In embodiments, R16 and R18 are hydrogen and R17 is substituted or unsubstituted pyridazinyl. In embodiments, R16 and R18 are hydrogen and R17 is substituted or unsubstituted triazinyl. In embodiments, R16 and R18 are hydrogen and R17 is substituted or unsubstituted pyrimidinyl. In embodiments, R16 and R18 are hydrogen and R17 is substituted or unsubstituted imidazolyl. In embodiments, R16 and R18 are hydrogen and R17 is substituted or unsubstituted pyrazinyl. In embodiments, R16 and R18 are hydrogen and R17 is substituted or unsubstituted oxazolyl. In embodiments, R16 and R18 are hydrogen and R17 is substituted or unsubstituted isoxazolyl. In embodiments, R16 and R18 are hydrogen and R17 is substituted or unsubstituted thiazolyl. In embodiments, R16 and R18 are hydrogen and R17 is substituted or unsubstituted furyl. In embodiments, R16 and R18 are hydrogen and R17 is substituted or unsubstituted thienyl. In embodiments, R16 and R18 are hydrogen and R17 is substituted or unsubstituted pyridyl. In embodiments, R16 and R18 are hydrogen and R17 is substituted or unsubstituted pyrimidyl. In embodiments, R16 and R18 are hydrogen and R17 is unsubstituted pyrrolyl. In embodiments, R16 and R18 are hydrogen and R17 is unsubstituted pyrazolyl. In embodiments, R16 and R18 are hydrogen and R17 is unsubstituted pyridazinyl. In embodiments, R16 and R18 are hydrogen and R17 is unsubstituted triazinyl. In embodiments, R16 and R18 are hydrogen and R17 is unsubstituted pyrimidinyl. In embodiments, R16 and R18 are hydrogen and R17 is unsubstituted imidazolyl. In embodiments, R16 and R18 are hydrogen and R17 is unsubstituted pyrazinyl. In embodiments, R16 and R18 are hydrogen and R17 is unsubstituted oxazolyl. In embodiments, R16 and R18 are hydrogen and R17 is unsubstituted isoxazolyl. In embodiments, R16 and R18 are hydrogen and R17 is unsubstituted thiazolyl. In embodiments, R16 and R18 are hydrogen and R17 is unsubstituted furyl. In embodiments, R16 and R18 are hydrogen and R17 is unsubstituted thienyl. In embodiments, R16 and R18 are hydrogen and R17 is unsubstituted pyridyl. In embodiments, R16 and R18 are hydrogen and R17 is unsubstituted pyrimidyl.
In embodiments, R16 is independently hydrogen, oxo, halogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —C(O)N(CH3)2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, —N3, substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted C6-C12 aryl, or substituted or unsubstituted 5 to 12 membered heteroaryl.
In embodiments, R17 is independently hydrogen, oxo, halogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —C(O)N(CH3)2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, —N3, substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted C6-C12 aryl, or substituted or unsubstituted 5 to 12 membered heteroaryl.
In embodiments, R18 is independently hydrogen, oxo, halogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —C(O)N(CH3)2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, —N3, substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted C6-C12 aryl, or substituted or unsubstituted 5 to 12 membered heteroaryl.
In embodiments, R16 is independently hydrogen, substituted or unsubstituted C1-C6 alkyl, or substituted or unsubstituted 2 to 6 membered heteroalkyl. In embodiments, R16 is independently hydrogen. In embodiments, R16 is independently substituted or unsubstituted C1-C6 alkyl. In embodiments, R16 is substituted methyl. In embodiments, R16 is substituted ethyl. In embodiments, R16 is substituted propyl. In embodiments, R16 is substituted isopropyl. In embodiments, R16 is substituted n-propyl. In embodiments, R16 is unsubstituted methyl. In embodiments, R16 is unsubstituted ethyl. In embodiments, R16 is unsubstituted propyl. In embodiments, R16 is unsubstituted isopropyl. In embodiments, R16 is unsubstituted n-propyl. In embodiments, R16 is independently substituted or unsubstituted 2 to 6 membered heteroalkyl. In embodiments, R16 is independently substituted or unsubstituted 2 to 3 membered heteroalkyl. In embodiments, R16 is independently hydrogen or —C(O)N(CH3)2. In embodiments, R16 is independently —C(O)N(CH3)2. In embodiments, R16 is independently hydrogen or substituted or unsubstituted C1-C6 alkyl. In embodiments, R16 is independently hydrogen or substituted or unsubstituted C1-C4 alkyl. In embodiments, R16 is independently hydrogen or substituted or unsubstituted C1-C2 alkyl. In embodiments, R16 is independently hydrogen or unsubstituted methyl.
In embodiments, R17 is independently hydrogen, substituted or unsubstituted C1-C6 alkyl, or substituted or unsubstituted 2 to 6 membered heteroalkyl. In embodiments, R17 is independently hydrogen. In embodiments, R17 is independently substituted or unsubstituted C1-C6 alkyl. In embodiments, R17 is substituted methyl. In embodiments, R17 is substituted ethyl. In embodiments, R17 is substituted propyl. In embodiments, R17 is substituted isopropyl. In embodiments, R17 is substituted n-propyl. In embodiments, R17 is unsubstituted methyl. In embodiments, R17 is unsubstituted ethyl. In embodiments, R17 is unsubstituted propyl. In embodiments, R17 is unsubstituted isopropyl. In embodiments, R17 is unsubstituted n-propyl. In embodiments, R17 is independently substituted or unsubstituted 2 to 6 membered heteroalkyl. In embodiments, R17 is independently substituted or unsubstituted 2 to 3 membered heteroalkyl. In embodiments, R17 is independently hydrogen or —C(O)N(CH3)2. In embodiments, R17 is independently —C(O)N(CH3)2. In embodiments, R17 is independently hydrogen or substituted or unsubstituted C1-C6 alkyl. In embodiments, R17 is independently hydrogen or substituted or unsubstituted C1-C4 alkyl. In embodiments, R17 is independently hydrogen or substituted or unsubstituted C1-C2 alkyl. In embodiments, R17 is independently hydrogen or unsubstituted methyl.
In embodiments, R17 is substituted or unsubstituted aryl. In embodiments, R17 is substituted or unsubstituted C6-C12 aryl. In embodiments, R17 is substituted or unsubstituted phenyl. In embodiments, R17 is unsubstituted phenyl.
In embodiments, R17 is substituted or unsubstituted heteroaryl. In embodiments, R17 is substituted or unsubstituted 5 to 6 membered heteroaryl. In embodiments, R17 is substituted or unsubstituted pyrrolyl. In embodiments, R17 is substituted or unsubstituted pyrazolyl. In embodiments, R17 is substituted or unsubstituted pyridazinyl. In embodiments, R17 is substituted or unsubstituted triazinyl. In embodiments, R17 is substituted or unsubstituted pyrimidinyl. In embodiments, R17 is substituted or unsubstituted imidazolyl. In embodiments, R17 is substituted or unsubstituted pyrazinyl. In embodiments, R17 is substituted or unsubstituted oxazolyl. In embodiments, R17 is substituted or unsubstituted isoxazolyl. In embodiments, R17 is substituted or unsubstituted thiazolyl. In embodiments, R17 is substituted or unsubstituted furyl. In embodiments, R17 is substituted or unsubstituted thienyl. In embodiments, R17 is substituted or unsubstituted pyridyl. In embodiments, R17 is substituted or unsubstituted pyrimidyl. In embodiments, R17 is substituted or unsubstituted benzothiazolyl. In embodiments, R17 is substituted or unsubstituted benzoxazoyl. In embodiments, R17 is substituted or unsubstituted benzimidazolyl. In embodiments, R17 is substituted or unsubstituted benzofuran. In embodiments, R17 is substituted or unsubstituted isobenzofuranyl. In embodiments, R17 is substituted or unsubstituted indolyl. In embodiments, R17 is substituted or unsubstituted isoindolyl. In embodiments, R17 is substituted or unsubstituted benzothiophenyl. In embodiments, R17 is substituted or unsubstituted isoquinolyl. In embodiments, R17 is substituted or unsubstituted quinoxalinyl. In embodiments, R17 is substituted or unsubstituted quinolyl.
In embodiments, R18 is independently hydrogen, substituted or unsubstituted C1-C6 alkyl, or substituted or unsubstituted 2 to 6 membered heteroalkyl. In embodiments, R18 is independently hydrogen. In embodiments, R18 is independently substituted or unsubstituted C1-C6 alkyl. In embodiments, R18 is substituted methyl. In embodiments, R18 is substituted ethyl. In embodiments, R18 is substituted propyl. In embodiments, R18 is substituted isopropyl. In embodiments, R18 is substituted n-propyl. In embodiments, R18 is unsubstituted methyl. In embodiments, R18 is unsubstituted ethyl. In embodiments, R18 is unsubstituted propyl. In embodiments, R18 is unsubstituted isopropyl. In embodiments, R18 is unsubstituted n-propyl. In embodiments, R18 is independently substituted or unsubstituted 2 to 6 membered heteroalkyl. In embodiments, R18 is independently substituted or unsubstituted 2 to 3 membered heteroalkyl. In embodiments, R18 is independently hydrogen or —C(O)N(CH3)2. In embodiments, R18 is independently —C(O)N(CH3)2. In embodiments, R18 is independently hydrogen or substituted or unsubstituted C1-C6 alkyl. In embodiments, R18 is independently hydrogen or substituted or unsubstituted C1-C4 alkyl. In embodiments, R18 is independently hydrogen or substituted or unsubstituted C1-C2 alkyl. In embodiments, R18 is independently hydrogen or unsubstituted methyl.
In embodiments, R19 and R20 are independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —COOH, —CONH2, —C(O)N(CH3)2, substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted C6-C12 aryl, or substituted or unsubstituted 5 to 12 membered heteroaryl.
In embodiments, R19 is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —COOH, —CONH2, —C(O)N(CH3)2, substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted C6-C12 aryl, or substituted or unsubstituted 5 to 12 membered heteroaryl.
In embodiments, R20 is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —COOH, —CONH2, —C(O)N(CH3)2, substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted C6-C12 aryl, or substituted or unsubstituted 5 to 12 membered heteroaryl.
In embodiments, R19 is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, substituted or unsubstituted C1-C6 alkyl, or substituted or unsubstituted 2 to 6 membered heteroalkyl. In embodiments, R19 is independently hydrogen. In embodiments, R19 is independently —CCl3. In embodiments, R19 is independently —CBr3. In embodiments, R19 is independently —CF3. In embodiments, R19 is independently —CI3. In embodiments, R19 is independently CHCl2. In embodiments, R19 is independently —CHBr2. In embodiments, R19 is independently —CHF2. In embodiments, R19 is independently —CHI2. In embodiments, R19 is independently —CH2Cl. In embodiments, R19 is independently —CH2Br. In embodiments, R19 is independently —CH2F. In embodiments, R19 is independently —CH2I. In embodiments, R19 is independently —CN. In embodiments, R19 is independently substituted or unsubstituted C1-C6 alkyl. In embodiments, R19 is substituted methyl. In embodiments, R19 is substituted ethyl. In embodiments, R19 is substituted propyl. In embodiments, R19 is substituted isopropyl. In embodiments, R19 is substituted n-propyl. In embodiments, R19 is unsubstituted methyl. In embodiments, R19 is unsubstituted ethyl. In embodiments, R19 is unsubstituted propyl. In embodiments, R19 is unsubstituted isopropyl. In embodiments, R19 is unsubstituted n-propyl. In embodiments, R19 is independently substituted or unsubstituted 2 to 6 membered heteroalkyl. In embodiments, R19 is independently substituted or unsubstituted 2 to 3 membered heteroalkyl. In embodiments, R19 is independently hydrogen or —C(O)N(CH3)2. In embodiments, R19 is independently —C(O)N(CH3)2. In embodiments, R19 is independently hydrogen or substituted or unsubstituted C1-C6 alkyl. In embodiments, R19 is independently hydrogen or substituted or unsubstituted C1-C4 alkyl. In embodiments, R19 is independently hydrogen or substituted or unsubstituted C1-C2 alkyl. In embodiments, R19 is independently hydrogen or unsubstituted methyl. In embodiments, R19 is independently hydrogen, —CF3, —CN, or unsubstituted methyl.
In embodiments, R19 is independently hydrogen, —CF3, —CN, or substituted or unsubstituted C1-C6 alkyl. In embodiments, R19 is independently hydrogen, —CF3, —CN, or unsubstituted C1-C6 alkyl. In embodiments, R19 is independently hydrogen, —CF3, —CN, or unsubstituted methyl. In embodiments, R19 is independently hydrogen or unsubstituted methyl. In embodiments, R19 is independently hydrogen or unsubstituted ethyl. In embodiments, R19 is independently hydrogen or unsubstituted propyl.
In embodiments, R20 is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, substituted or unsubstituted C1-C6 alkyl, or substituted or unsubstituted 2 to 6 membered heteroalkyl. In embodiments, R20 is independently hydrogen. In embodiments, R20 is independently —CCl3. In embodiments, R20 is independently —CBr3. In embodiments, R20 is independently —CF3. In embodiments, R20 is independently —CI3. In embodiments, R20 is independently CHCl2. In embodiments, R20 is independently —CHBr2. In embodiments, R20 is independently —CHF2. In embodiments, R20 is independently —CHI2. In embodiments, R20 is independently —CH2Cl. In embodiments, R20 is independently —CH2Br. In embodiments, R20 is independently —CH2F. In embodiments, R20 is independently —CH2I. In embodiments, R20 is independently —CN. In embodiments, R20 is independently substituted or unsubstituted C1-C6 alkyl. In embodiments, R20 is substituted methyl. In embodiments, R20 is substituted ethyl. In embodiments, R20 is substituted propyl. In embodiments, R20 is substituted isopropyl. In embodiments, R20 is substituted n-propyl. In embodiments, R20 is unsubstituted methyl. In embodiments, R20 is unsubstituted ethyl. In embodiments, R20 is unsubstituted propyl. In embodiments, R20 is unsubstituted isopropyl. In embodiments, R20 is unsubstituted n-propyl. In embodiments, R20 is independently substituted or unsubstituted 2 to 6 membered heteroalkyl. In embodiments, R20 is independently substituted or unsubstituted 2 to 3 membered heteroalkyl. In embodiments, R20 is independently hydrogen or —C(O)N(CH3)2. In embodiments, R20 is independently —C(O)N(CH3)2. In embodiments, R20 is independently hydrogen or substituted or unsubstituted C1-C6 alkyl. In embodiments, R20 is independently hydrogen or substituted or unsubstituted C1-C4 alkyl. In embodiments, R20 is independently hydrogen or substituted or unsubstituted C1-C2 alkyl. In embodiments, R20 is independently hydrogen or unsubstituted methyl. In embodiments, R20 is independently hydrogen, —CF3, —CN, or unsubstituted methyl.
In embodiments, R20 is independently hydrogen, —CF3, —CN, or substituted or unsubstituted C1-C6 alkyl. In embodiments, R20 is independently hydrogen, —CF3, —CN, or unsubstituted C1-C6 alkyl. In embodiments, R20 is independently hydrogen, —CF3, —CN, or unsubstituted methyl. In embodiments, R20 is independently hydrogen or unsubstituted methyl. In embodiments, R20 is independently hydrogen or unsubstituted ethyl. In embodiments, R20 is independently hydrogen or unsubstituted propyl.
In embodiments, R1A is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl.
In embodiments, R1A is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted C6-C12 aryl, or substituted or unsubstituted 5 to 12 membered heteroaryl.
In embodiments, R1A is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, substituted or unsubstituted C1-C4 alkyl, or substituted or unsubstituted 2 to 4 membered heteroalkyl. In embodiments, R1A is independently hydrogen, substituted or unsubstituted C1-C4 alkyl, or substituted or unsubstituted 2 to 4 membered heteroalkyl. In embodiments, R1A is independently hydrogen. In embodiments, R1A is independently substituted or unsubstituted C1-C4 alkyl. In embodiments, R1A is independently substituted or unsubstituted 2 to 4 membered heteroalkyl. In embodiments, R1A is independently unsubstituted methyl.
In embodiments, R1B is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl.
In embodiments, R1B is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted C6-C12 aryl, or substituted or unsubstituted 5 to 12 membered heteroaryl.
In embodiments, R1B is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, substituted or unsubstituted C1-C4 alkyl, or substituted or unsubstituted 2 to 4 membered heteroalkyl. In embodiments, R1B is independently hydrogen, substituted or unsubstituted C1-C4 alkyl, or substituted or unsubstituted 2 to 4 membered heteroalkyl. In embodiments, R1B is independently hydrogen. In embodiments, R1B is independently substituted or unsubstituted C1-C4 alkyl. In embodiments, R1B is independently substituted or unsubstituted 2 to 4 membered heteroalkyl. In embodiments, R1B is independently unsubstituted methyl.
In embodiments, R1A and R1B substituents bonded to the same nitrogen atom may optionally be joined to form a substituted or unsubstituted heterocycloalkyl or substituted or unsubstituted heteroaryl.
In embodiments, R1A and R1B substituents bonded to the same nitrogen atom may optionally be joined to form a substituted or unsubstituted 3 to 6 membered heterocycloalkyl or substituted or unsubstituted 5 to 12 membered heteroaryl.
In embodiments, R1C is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl.
In embodiments, R1C is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted C6-C12 aryl, or substituted or unsubstituted 5 to 12 membered heteroaryl.
In embodiments, R1C is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, substituted or unsubstituted C1-C4 alkyl, or substituted or unsubstituted 2 to 4 membered heteroalkyl. In embodiments, R1C is independently hydrogen, substituted or unsubstituted C1-C4 alkyl, or substituted or unsubstituted 2 to 4 membered heteroalkyl. In embodiments, R1C is independently hydrogen. In embodiments, R1C is independently substituted or unsubstituted C1-C4 alkyl. In embodiments, R1C is independently substituted or unsubstituted 2 to 4 membered heteroalkyl. In embodiments, R1C is independently unsubstituted methyl.
In embodiments, R1D is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl.
In embodiments, R1D is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted C6-C12 aryl, or substituted or unsubstituted 5 to 12 membered heteroaryl.
In embodiments, R1D is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, substituted or unsubstituted C1-C4 alkyl, or substituted or unsubstituted 2 to 4 membered heteroalkyl. In embodiments, R1D is independently hydrogen, substituted or unsubstituted C1-C4 alkyl, or substituted or unsubstituted 2 to 4 membered heteroalkyl. In embodiments, R1D is independently hydrogen. In embodiments, R1D is independently substituted or unsubstituted C1-C4 alkyl. In embodiments, R1D is independently substituted or unsubstituted 2 to 4 membered heteroalkyl. In embodiments, R1D is independently unsubstituted methyl.
In embodiments, R2A is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl.
In embodiments, R2A is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted C6-C12 aryl, or substituted or unsubstituted 5 to 12 membered heteroaryl.
In embodiments, R2A is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, substituted or unsubstituted C1-C4 alkyl, or substituted or unsubstituted 2 to 4 membered heteroalkyl. In embodiments, R2A is independently hydrogen, substituted or unsubstituted C1-C4 alkyl, or substituted or unsubstituted 2 to 4 membered heteroalkyl. In embodiments, R2A is independently hydrogen. In embodiments, R2A is independently substituted or unsubstituted C1-C4 alkyl. In embodiments, R2A is independently substituted or unsubstituted 2 to 4 membered heteroalkyl. In embodiments, R2A is independently unsubstituted methyl.
In embodiments, R2B is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl.
In embodiments, R2B is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted C6-C12 aryl, or substituted or unsubstituted 5 to 12 membered heteroaryl.
In embodiments, R2B is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, substituted or unsubstituted C1-C4 alkyl, or substituted or unsubstituted 2 to 4 membered heteroalkyl. In embodiments, R2B is independently hydrogen, substituted or unsubstituted C1-C4 alkyl, or substituted or unsubstituted 2 to 4 membered heteroalkyl. In embodiments, R2B is independently hydrogen. In embodiments, R2B is independently substituted or unsubstituted C1-C4 alkyl. In embodiments, R2B is independently substituted or unsubstituted 2 to 4 membered heteroalkyl. In embodiments, R2B is independently unsubstituted methyl.
In embodiments, R2A and R2B substituents bonded to the same nitrogen atom may optionally be joined to form a substituted or unsubstituted heterocycloalkyl or substituted or unsubstituted heteroaryl.
In embodiments, R2A and R2B substituents bonded to the same nitrogen atom may optionally be joined to form a substituted or unsubstituted 3 to 6 membered heterocycloalkyl or substituted or unsubstituted 5 to 12 membered heteroaryl.
In embodiments, R2C is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl.
In embodiments, R2C is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted C6-C12 aryl, or substituted or unsubstituted 5 to 12 membered heteroaryl.
In embodiments, R2C is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, substituted or unsubstituted C1-C4 alkyl, or substituted or unsubstituted 2 to 4 membered heteroalkyl. In embodiments, R2C is independently hydrogen, substituted or unsubstituted C1-C4 alkyl, or substituted or unsubstituted 2 to 4 membered heteroalkyl. In embodiments, R2C is independently hydrogen. In embodiments, R2C is independently substituted or unsubstituted C1-C4 alkyl. In embodiments, R2C is independently substituted or unsubstituted 2 to 4 membered heteroalkyl. In embodiments, R2C is independently unsubstituted methyl.
In embodiments, R2D is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl.
In embodiments, R2D is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted C6-C12 aryl, or substituted or unsubstituted 5 to 12 membered heteroaryl.
In embodiments, R2D is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, substituted or unsubstituted C1-C4 alkyl, or substituted or unsubstituted 2 to 4 membered heteroalkyl. In embodiments, R2D is independently hydrogen, substituted or unsubstituted C1-C4 alkyl, or substituted or unsubstituted 2 to 4 membered heteroalkyl. In embodiments, R2D is independently hydrogen. In embodiments, R2D is independently substituted or unsubstituted C1-C4 alkyl. In embodiments, R2D is independently substituted or unsubstituted 2 to 4 membered heteroalkyl. In embodiments, R2D is independently unsubstituted methyl.
In embodiments, R1.2 is independently hydrogen, halogen, —CCl3, —CBr3, —CF3, —CI3, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —OCI3, —N3, substituted or unsubstituted C1-C3 alkyl, or substituted or unsubstituted 2 to 4 membered heteroalkyl. In embodiments, R1.2 is independently hydrogen. In embodiments, R1.2 is independently halogen. In embodiments, R1.2 is independently —F. In embodiments, R1.2 is independently —Cl. In embodiments, R1.2 is independently-Br. In embodiments, R1.2 is independently —I. In embodiments, R1.2 is independently —CCl3. In embodiments, R1.2 is independently —CBr3. In embodiments, R1.2 is independently —CF3. In embodiments, R1.2 is independently —CI3. In embodiments, R1.2 is independently —CN. In embodiments, R1.2 is independently —OH. In embodiments, R1.2 is independently —NH2. In embodiments, R1.2 is independently —COOH. In embodiments, R1.2 is independently —CONH2. In embodiments, R1.2 is independently —OCCl3. In embodiments, R1.2 is independently —OCF3. In embodiments, R1.2 is independently —OCBr3. In embodiments, R1.2 is independently —OCI3. In embodiments, R1.2 is independently —N3. In embodiments, R1.2 is independently substituted or unsubstituted C1-C3 alkyl. In embodiments, R1.2 is independently unsubstituted methyl. In embodiments, R1.2 is independently unsubstituted ethyl. In embodiments, R1.2 is independently unsubstituted propyl. In embodiments, R1.2 is independently substituted or unsubstituted 2 to 4 membered heteroalkyl. In embodiments, R1.2 is independently unsubstituted 2 to 4 membered heteroalkyl.
In embodiments, R1.3 is independently hydrogen, halogen, —CCl3, —CBr3, —CF3, —CI3, —CN, —OH, —NH2, -COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —OCI3, —N3, substituted or unsubstituted C1-C3 alkyl, or substituted or unsubstituted 2 to 4 membered heteroalkyl. In embodiments, R1.3 is independently halogen. In embodiments, R1.3 is independently —F. In embodiments, R1.3 is independently —Cl. In embodiments, R1.3 is independently—Br. In embodiments, R1.3 is independently —I. In embodiments, R1.3 is independently —CCl3. In embodiments, R1.3 is independently —CBr3. In embodiments, R1.3 is independently —CF3. In embodiments, R1.3 is independently —CI3. In embodiments, R1.3 is independently —CN. In embodiments, R1.3 is independently —OH. In embodiments, R1.3 is independently —NH2. In embodiments, R1.3 is independently -COOH. In embodiments, R1.3 is independently —CONH2. In embodiments, R1.3 is independently —OCCl3. In embodiments, R1.3 is independently —OCF3. In embodiments, R1.3 is independently —OCBr3. In embodiments, R1.3 is independently —OCI3. In embodiments, R1.3 is independently —N3. In embodiments, R1.3 is independently substituted or unsubstituted C1-C3 alkyl. In embodiments, R1.3 is independently unsubstituted methyl. In embodiments, R1.3 is independently unsubstituted ethyl. In embodiments, R1.3 is independently unsubstituted propyl. In embodiments, R1.3 is independently substituted or unsubstituted 2 to 4 membered heteroalkyl. In embodiments, R1.3 is independently unsubstituted 2 to 4 membered heteroalkyl.
In embodiments, R1.2 and R1.3 substituents on adjacent carbons are joined to form a substituted or unsubstituted phenyl, or substituted or unsubstituted 5 to 6 membered heteroaryl. In embodiments, R1.2 and R1.3 substituents on adjacent carbons are joined to form a substituted or unsubstituted phenyl. In embodiments, R1.2 and R1.3 substituents on adjacent carbons are joined to form an R11-substituted phenyl. In embodiments, R1.2 and R1.3 substituents on adjacent carbons are joined to form an unsubstituted phenyl. In embodiments, R1.2 and R1.3 substituents on adjacent carbons are joined to form a substituted or unsubstituted 5 to 6 membered heteroaryl. In embodiments, R1.2 and R1.3 substituents on adjacent carbons are joined to form a R11-substituted or unsubstituted 5 to 6 membered heteroaryl. In embodiments, R1.2 and R1.3 substituents on adjacent carbons are joined to form an unsubstituted 5 to 6 membered heteroaryl.
In embodiments, R1.4 is independently hydrogen, halogen, —CCl3, —CBr3, —CF3, —CI3, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —OCI3, —N3, substituted or unsubstituted C1-C3 alkyl, or substituted or unsubstituted 2 to 4 membered heteroalkyl. In embodiments, R1.4 is independently halogen. In embodiments, R1.4 is independently —F. In embodiments, R1.4 is independently —Cl. In embodiments, R1.4 is independently —Br. In embodiments, R1.4 is independently —I. In embodiments, R1.4 is independently —CCl3. In embodiments, R1.4 is independently —CBr3. In embodiments, R1.4 is independently —CF3. In embodiments, R1.4 is independently —CI3. In embodiments, R1.4 is independently —CN. In embodiments, R1.4 is independently —OH. In embodiments, R1.4 is independently —NH2. In embodiments, R1.4 is independently -COOH. In embodiments, R1.4 is independently —CONH2. In embodiments, R1.4 is independently —OCCl3. In embodiments, R1.4 is independently —OCF3. In embodiments, R1.4 is independently —OCBr3. In embodiments, R1.4 is independently —OCI3. In embodiments, R1.4 is independently —N3. In embodiments, R1.4 is independently substituted or unsubstituted C1-C3 alkyl. In embodiments, R1.4 is independently unsubstituted methyl. In embodiments, R1.4 is independently unsubstituted ethyl. In embodiments, R1.4 is independently unsubstituted propyl. In embodiments, R1.4 is independently substituted or unsubstituted 2 to 4 membered heteroalkyl. In embodiments, R1.4 is independently unsubstituted 2 to 4 membered heteroalkyl.
In embodiments, R1.5 is independently hydrogen, halogen, —CCl3, —CBr3, —CF3, —CI3, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —OCI3, —N3, substituted or unsubstituted C1-C3 alkyl, or substituted or unsubstituted 2 to 4 membered heteroalkyl. In embodiments, R1.5 is independently halogen. In embodiments, R1.5 is independently —F. In embodiments, R1.5 is independently —Cl. In embodiments, R1.5 is independently —Br. In embodiments, R1.5 is independently —I. In embodiments, R1.5 is independently —CCl3. In embodiments, R1.5 is independently —CBr3. In embodiments, R1.5 is independently —CF3. In embodiments, R1.5 is independently —CI3. In embodiments, R1.5 is independently —CN. In embodiments, R1.5 is independently —OH. In embodiments, R1.5 is independently —NH2. In embodiments, R1.5 is independently —COOH. In embodiments, R1.5 is independently —CONH2. In embodiments, R1.5 is independently —OCCl3. In embodiments, R1.5 is independently —OCF3. In embodiments, R1.5 is independently —OCBr3. In embodiments, R1.5 is independently —OCI3. In embodiments, R1.5 is independently —N3. In embodiments, R1.5 is independently substituted or unsubstituted C1-C3 alkyl. In embodiments, R1.5 is independently unsubstituted methyl. In embodiments, R1.5 is independently unsubstituted ethyl. In embodiments, R1.5 is independently unsubstituted propyl. In embodiments, R1.5 is independently substituted or unsubstituted 2 to 4 membered heteroalkyl. In embodiments, R1.5 is independently unsubstituted 2 to 4 membered heteroalkyl.
In embodiments, R1.4 is hydrogen and R1.5 is —F. In embodiments, R1.4 is —F and R1.5 is hydrogen. In embodiments, R1.4 and R1.5 are —F. In embodiments, R1.4 and R1.5 are hydrogen.
In embodiments, W1 is independently —O—. In embodiments, W1 is independently —NH—. In embodiments, 1 is independently —NR2—. In embodiments, W2 is independently ═N—. In embodiments, 2 is independently ═CH—. In embodiments, W2 is independently ═CR2—. In embodiments, W3 is independently ═N—. In embodiments, 3 is independently ═CH—. In embodiments, W3 is independently ═CR2—.
In embodiments, R2 is independently oxo, halogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, , —CN, —OH, —NH2, —COOH, —CONH2, —C(O)N(CH3)2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, —N3, substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted C6-C12 aryl, or substituted or unsubstituted 5 to 12 membered heteroaryl.
In embodiments, R11 is independently oxo, halogen, —CX113, —CHX112, —CH2X11, —OCX113, —OCH2X11, —OCHX112, —CN, —OH, —NH2, —COOH, —CONH2, —C(O)N(CH3)2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —N3, substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted C6-C12 aryl, or substituted or unsubstituted 5 to 12 membered heteroaryl.
In embodiments, R11 is independently oxo, halogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, , —CN, —OH, —NH2, —COOH, —CONH2, —C(O)N(CH3)2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, —N3, substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted C6-C12 aryl, or substituted or unsubstituted 5 to 12 membered heteroaryl;
In embodiments, R21 is independently oxo, halogen, —CX213, —CHX212, —CH2X21, —OCX213, —OCH2X21, —OCHX212, —CN, —OH, —NH2, —COOH, —CONH2, —C(O)N(CH3)2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —N3, substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted C6-C12 aryl, or substituted or unsubstituted 5 to 12 membered heteroaryl;
In embodiments, R21 is independently oxo, halogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —C(O)N(CH3)2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, —N3, substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted C6-C12 aryl, or substituted or unsubstituted 5 to 12 membered heteroaryl.
In embodiments, R2 is independently halogen, —OCX23, —OCH2X2, —OCHX22, unsubstituted C1—C3 alkyl, or unsubstituted 5 to 6 membered heteroaryl. In embodiments, R11 is independently halogen, —OCX113, —OCH2X11, -OCHX112, unsubstituted C1-C3 alkyl, or unsubstituted 5 to 6 membered heteroaryl. In embodiments, R21 is independentlyhalogen, —OCX213, —OCH2X21, —OCHX212, unsubstituted C1—C3 alkyl, or unsubstituted 5 to 6 membered heteroaryl.
In embodiments, R11 is independently halogen, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OC H2Br, —OCH2I, —OCH2F, unsubstituted C1-C3 alkyl, or unsubstituted 5 to 6 membered heteroaryl. In embodiments, R11 is independently halogen. In embodiments, R11 is independently —F. In embodiments, R11 is independently —Cl. In embodiments, R11 is independently —Br. In embodiments, R11 is independently —I. In embodiments, R11 is independently —OCCl3. In embodiments, R11 is independently —OCF3. In embodiments, R11 is independently —OCBr3. In embodiments, R11 is independently —OCI3. In embodiments, R11 is independently —OCHCl2. In embodiments, R11 is independently —OCHBr2. In embodiments, R11 is independently —OCHI2. In embodiments, R11 is independently —OCHF2. In embodiments, R11 is independently —OCH2Cl. In embodiments, R11 is independently —OCH2Br. In embodiments, R11 is independently —OCH2I. In embodiments, R11 is independently —OCH2F. In embodiments, R11 is independently unsubstituted methyl. In embodiments, R11 is independently unsubstituted ethyl. In embodiments, R11 is independently unsubstituted propyl. In embodiments, R11 is independently unsubstituted 5 to 6 membered heteroaryl. In embodiments, R11 is independently unsubstituted 5 membered heteroaryl. In embodiments, R11 is independently unsubstituted 6 membered heteroaryl.
In embodiments, R11.1 is independently oxo, halogen, —CX113, —CHX112, —CH2X11, —OCX113, —OCH2X11, —OCHX112, —CN, —OH, —NH2, —COOH, —CONH2, —C(O)N(CH3)2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —N3, substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted C6-C12 aryl, or substituted or unsubstituted 5 to 12 membered heteroaryl.
In embodiments, R11.1 is independently oxo, halogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, , —CN, —OH, —NH2, —COOH, —CONH2, —C(O)N(CH3)2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHC12, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, —N3, substituted or unsubstituted C1-C6 alkyl, substituted or unsubstituted 2 to 6 membered heteroalkyl, substituted or unsubstituted C3-C6 cycloalkyl, substituted or unsubstituted 3 to 6 membered heterocycloalkyl, substituted or unsubstituted C6-C12 aryl, or substituted or unsubstituted 5 to 12 membered heteroaryl.
In embodiments, R11.1 is independently halogen, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OC H2Br, —OCH2I, —OCH2F, unsubstituted C1-C3 alkyl, or unsubstituted 5 to 6 membered heteroaryl. In embodiments, R11.1 is independently halogen. In embodiments, R11.1 is independently —F. In embodiments, R11.1 is independently —Cl. In embodiments, R11.1 is independently —Br. In embodiments, R11.1 is independently —I. In embodiments, R11.1 is independently —OCCl3. In embodiments, R11.1 is independently —OCF3. In embodiments, R11.1 is independently —OCBr3. In embodiments, R11.1 is independently —OCI3. In embodiments, R11.1 is independently —OCHCl2. In embodiments, R11.1 is independently —OCHBr2. In embodiments, R11.1 is independently —OCHI2. In embodiments, R11.1 is independently —OCHF2. In embodiments, R11.1 is independently —OCH2Cl. In embodiments, R11.1 is independently —OCH2Br. In embodiments, R11.1 is independently —OCH2I. In embodiments, R11.1 is independently —OCH2F. In embodiments, R11.1 is independently unsubstituted methyl. In embodiments, R11.1 is independently unsubstituted ethyl. In embodiments, R11.1 is independently unsubstituted propyl. In embodiments, R11.1 is independently unsubstituted 5 to 6 membered heteroaryl. In embodiments, R11.1 is independently unsubstituted 5 membered heteroaryl. In embodiments, R11.1 is independently unsubstituted 6 membered heteroaryl.
In embodiments, R21 is independently halogen, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OC H2Br, —OCH2I, —OCH2F, unsubstituted C1-C3 alkyl, or unsubstituted 5 to 6 membered heteroaryl. In embodiments, R21 is independently halogen. In embodiments, R21 is independently —F. In embodiments, R21 is independently —Cl. In embodiments, R21 is independently —Br. In embodiments, R21 is independently —I. In embodiments, R21 is independently —OCCl3. In embodiments, R21 is independently —OCF3. In embodiments, R21 is independently —OCBr3. In embodiments, R21 is independently —OCI3. In embodiments, R21 is independently —OCHCl2. In embodiments, R21 is independently —OCHBr2. In embodiments, R21 is independently —OCHI2. In embodiments, R21 is independently —OCHF2. In embodiments, R21 is independently —OCH2Cl. In embodiments, R21 is independently —OCH2Br. In embodiments, R21 is independently —OCH2I. In embodiments, R21 is independently —OCH2F. In embodiments, R21 is independently unsubstituted methyl. In embodiments, R21 is independently unsubstituted ethyl. In embodiments, R21 is independently unsubstituted propyl. In embodiments, R21 is independently unsubstituted 5 to 6 membered heteroaryl. In embodiments, R21 is independently unsubstituted 5 membered heteroaryl. In embodiments, R21 is independently unsubstituted 6 membered heteroaryl.
In embodiments, R2.1 is independently hydrogen, —OCCl3, —OCF3, —OCBr3, —OCI3, or unsubstituted 5 to 6 membered heteroaryl. In embodiments, R2.1 is independently hydrogen. In embodiments, R2.1 is independently —OCCl3. In embodiments, R2.1 is independently —OCF3. In embodiments, R2.1 is independently —OCBr3. In embodiments, R2.1 is independently —OCI3. In embodiments, R2.1 is independently unsubstituted 5 to 6 membered heteroaryl. In embodiments, R2.1 is independently unsubstituted 5 membered heteroaryl. In embodiments, R2.1 is independently unsubstituted 6 membered heteroaryl. In embodiments, R2.1 is independently pyrrolyl, pyrazolyl, pyridazinyl, triazinyl, pyrimidinyl, imidazolyl, pyrazinyl, oxazolyl, isoxazolyl, thiazolyl, furyl, thienyl, pyridyl, pyrimidyl, benzothiazolyl, benzoxazoyl, benzimidazolyl, benzofuran, isobenzofuranyl, indolyl, or isoindolyl. In embodiments, R2.1 is independently phenyl, benzimidazolyl, or indolyl. In embodiments, R2.1 is independently pyrrolyl. In embodiments, R2.1 is independently pyrazolyl. In embodiments, R2.1 is independently pyridazinyl. In embodiments, R2.1 is independently triazinyl. In embodiments, R2.1 is independently pyrimidinyl. In embodiments, R2.1 is independently imidazolyl. In embodiments, R2.1 is independently pyrazinyl. In embodiments, R2.1 is independently oxazolyl. In embodiments, R2.1 is independently isoxazolyl. In embodiments, R2.1 is independently thiazolyl. In embodiments, R2.1 is independently furyl. In embodiments, R2.1 is independently thienyl. In embodiments, R2.1 is independently pyridyl. In embodiments, R2.1 is independently pyrimidyl. In embodiments, R2.1 is independently benzothiazolyl. In embodiments, R2.1 is independently benzoxazoyl. In embodiments, R2.1 is independently benzimidazolyl. In embodiments, R2.1 is independently benzofuran. In embodiments, R2.1 is independently isobenzofuranyl. In embodiments, R2.1 is independently indolyl. In embodiments, R2.1 is independently isoindolyl. In embodiments, R2.1 is independently unsubstituted pyrrolyl, pyrazolyl, pyridazinyl, triazinyl, pyrimidinyl, imidazolyl, pyrazinyl, oxazolyl, isoxazolyl, thiazolyl, furyl, thienyl, pyridyl, pyrimidyl, benzothiazolyl, benzoxazoyl, benzimidazolyl, benzofuran, isobenzofuranyl, indolyl, or isoindolyl. In embodiments, R2.1 is independently unsubstituted phenyl, benzimidazolyl, or indolyl. In embodiments, R2.1 is independently unsubstituted pyrrolyl. In embodiments, R2.1 is independently unsubstituted pyrazolyl. In embodiments, R2.1 is independently unsubstituted pyridazinyl. In embodiments, R2.1 is independently unsubstituted triazinyl. In embodiments, R2.1 is independently unsubstituted pyrimidinyl. In embodiments, R2.1 is independently unsubstituted imidazolyl. In embodiments, R2.1 is independently unsubstituted pyrazinyl. In embodiments, R2.1 is independently unsubstituted oxazolyl. In embodiments, R2.1 is independently unsubstituted isoxazolyl. In embodiments, R2.1 is independently unsubstituted thiazolyl. In embodiments, R2.1 is independently unsubstituted furyl. In embodiments, R2.1 is independently unsubstituted thienyl. In embodiments, R2.1 is independently unsubstituted pyridyl. In embodiments, R2.1 is independently unsubstituted pyrimidyl. In embodiments, R2.1 is independently unsubstituted benzothiazolyl. In embodiments, R2.1 is independently unsubstituted benzoxazoyl. In embodiments, R2.1 is independently unsubstituted benzimidazolyl. In embodiments, R2.1 is independently unsubstituted benzofuran. In embodiments, R2.1 is independently unsubstituted isobenzofuranyl. In embodiments, R2.1 is independently unsubstituted indolyl. In embodiments, R2.1 is independently unsubstituted isoindolyl.
In embodiments, R2.2 is independently hydrogen, —F, —Cl, —Br, or —I. In embodiments, R2.2 is independently hydrogen. In embodiments, R2.2 is independently —F. In embodiments, R2.2 is independently —Cl. In embodiments, R2.2 is independently —Br. In embodiments, R2.2 is independently —I.
In embodiments, z1 is an integer from 0 to 9. In embodiments, z1 is 0. In embodiments, z1 is 1. In embodiments, z1 is 2. In embodiments, z1 is 3. In embodiments, z1 is 4. In embodiments, z1 is 5. In embodiments, z1 is 6. In embodiments, z1 is 7. In embodiments, z1 is 8. In embodiments, z1 is 9. In embodiments, z2 is an integer from 0 to 6. In embodiments, z2 is 0. In embodiments, z2 is 1. In embodiments, z2 is 2. In embodiments, z2 is 3. In embodiments, z2 is 4. In embodiments, z2 is 5. In embodiments, z2 is 6. In embodiments, z6 is 1 or 2. In embodiments, z6 is 1. In embodiments, z6 is 2. In embodiments, z11 is an integer from 0 to 4. In embodiments, z11 is 0. In embodiments, z11 is 1. In embodiments, z11 is 2. In embodiments, z11 is 3. In embodiments, z11 is 4. In embodiments, z21 is an integer from 0 to 5. In embodiments, z21 is 0. In embodiments, z21 is 1. In embodiments, z21 is 2. In embodiments, z21 is 3. In embodiments, z21 is 4. In embodiments, z21 is 5.
In embodiments, n1 and n2 are independently an integer from 0 to 4. In embodiments, n1 is independently 0. In embodiments, n1 is independently 1. In embodiments, n1 is independently 2. In embodiments, n1 is independently 3. In embodiments, n1 is independently 4. In embodiments, m1, m2, v1, and v2 are independently 1 or 2. In embodiments, m1 is independently 1. In embodiments, m1 is independently 2. In embodiments, m2 is independently 1. In embodiments, m2 is independently 2. In embodiments, v1 is independently 1. In embodiments, v1 is independently 2. In embodiments, v2 is independently 1. In embodiments, v2 is independently 2.
In embodiments, X1 and X2 are independently —F, —Cl, —Br, or —I. In embodiments, X1 is independently —F, —Cl, —Br, or —I. In embodiments, X1 is independently —F. In embodiments, X1 is independently —Cl. In embodiments, X1 is independently —Br. In embodiments, X1 is independently —I. In embodiments, X2 is independently —F, —Cl, —Br, or —I. In embodiments, X2 is independently —F. In embodiments, X2 is independently —Cl. In embodiments, X2 is independently —Br. In embodiments, X2 is independently —I. In embodiments, X11 is independently —F, —Cl, —Br, or —I. In embodiments, X21 is independently —F, —Cl, —Br, or —I. In embodiments, X11 is independently —F. In embodiments, X11 is independently —Cl. In embodiments, X11 is independently —Br. In embodiments, X11 is independently —I. In embodiments, X21 is independently —F. In embodiments, X21 is independently —Cl. In embodiments, X21 is independently —Br. In embodiments, X21 is independently —I.
In embodiments, R1 is independently halogen, —CX13, —CHX12, —CH2X1, —OCX13, —OCH2X1, —OCHX12, —CN, —SOn1R1D, —SOv1NR1AR1B, —NR1CNR1AR1B, —ONR1AR1B, —NHC(O)NR1CNR1AR1B, —NHC(O)NR1AR1B, —N(O)m1, —NR1AR1B, —C(O)R1C, —C(O)—OR1C, —C(O) NR1AR1B, —OR1D, —NR1ASO2R1D, —NR1AC(O)R1C, —NR1AC(O)OR1C, —NR1AOR1C, —SF5, —N3, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted alkyl (e.g., C1-C8, C1-C6, C1-C4, or C1-C2), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroalkyl (e.g., 2 to 8 membered, 2 to 6 membered, 4 to 6 membered, 2 to 3 membered, or 4 to 5 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted cycloalkyl (e.g., C3-C8, C3-C6, C4-C6, or C5-C6), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered, 3 to 6 membered, 4 to 6 membered, 4 to 5 membered, or 5 to 6 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted aryl (e.g., C6-C10 or phenyl), or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroaryl (e.g., 5 to 10 membered, 5 to 9 membered, or 5 to 6 membered); two adjacent R1 substituents on adjacent carbons may optionally be joined to form a substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted cycloalkyl (e.g., C3-C8, C3-C6, C4-C6, or C5-C6), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered, 3 to 6 membered, 4 to 6 membered, 4 to 5 membered, or 5 to 6 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted aryl (e.g., C6-C10 or phenyl), or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroaryl (e.g., 5 to 10 membered, 5 to 9 membered, or 5 to 6 membered).
In embodiments, R1 is independently halogen, —CX13, —CHX12, —CH2X1, —OCX13, —OCH2X1, —OCHX12, —CN, —SOn1R1D, —SOv1NR1AR1B, —NR1CNR1AR1B, —ONR1AR1B, —NHC(O)NR1CNR1AR1B, —NHC(O)NR1AR1B, —N(O)m1, —NR1AR1B, —C(O)R1C, —C(O)—OR1C, —C(O) NR1AR1B, —OR1D, —NR1ASO2R1D, —NR1AC(O)R1C, —NR1AC(O)OR1C, —NR1AOR1C, —SF5, —N3, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted C1-C6 alkyl, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted 2 to 6 membered heteroalkyl, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted C3-C6 cycloalkyl, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted 3 to 6 membered heterocycloalkyl, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted C6-C10 aryl, or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted 5 to 10 membered heteroaryl; two adjacent R1 substituents on adjacent carbons may optionally be joined to form a substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted C3-C6 cycloalkyl, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted 3 to 6 membered heterocycloalkyl, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted phenyl, or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted 5 to 6 membered heteroaryl.
In embodiments, a substituted R1 (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R1 is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different. In embodiments, when R1 is substituted, it is substituted with at least one substituent group. In embodiments, when R1 is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when R1 is substituted, it is substituted with at least one lower substituent group.
In embodiments, R2 is independently oxo, halogen, —CX23, —CHX22, —CH2X2, —OCX23, —OCH2X2, —OCHX22, —CN, —SOn2R2D, —SOv2NR2AR2B, —NR2CNR2AR2B, —ONR2AR2B, —NHC(O)NR2CNR2AR2B,—NHC(O)NR2AR2B, —N(O)m2, —NR2AR2B, —C(O)R2C, —C(O)—OR2C, —C(O) NR2AR2B, —OR2D, —NR2ASO2R2D, —NR2AC(O)R2C, —NR2AC(O)OR2C, —NR2AOR2C, —SF5, —N3, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted alkyl (e.g., C1-C8, C1-C6, C1-C4, or C1-C2), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroalkyl (e.g., 2 to 8 membered, 2 to 6 membered, 4 to 6 membered, 2 to 3 membered, or 4 to 5 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted cycloalkyl (e.g., C3-C8, C3-C6, C4-C6, or C5-C6), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered, 3 to 6 membered, 4 to 6 membered, 4 to 5 membered, or 5 to 6 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted aryl (e.g., C6-C10 or phenyl), or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroaryl (e.g., 5 to 10 membered, 5 to 9 membered, or 5 to 6 membered).
In embodiments, R2 is independently oxo, halogen, —CX23, —CHX22, —CH2X2, —OCX23, —OCH2X2, —OCHX22, —CN, —SOn2R2D, —SOv2NR2AR2B, —NR2CNR2AR2B, —ONR2AR2B, —NHC(O)NR2CNR2AR2B,—NHC(O)NR2AR2B, —N(O)m2, —NR2AR2B, —C(O)R2C, —C(O)—OR2C, —C(O) NR2AR2B, —OR2D, —NR2ASO2R2D, —NR2AC(O)R2C, —NR2AC(O)OR2C, —NR2AOR2C, —SF5, —N3, substituted or unsubstituted C1-C6 alkyl, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted 2 to 6 membered heteroalkyl, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted C3-C6 cycloalkyl, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted 3 to 6 membered heterocycloalkyl, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted C6-C10 aryl, or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted 5 to 10 membered heteroaryl.
In embodiments, a substituted R2 (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R2 is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different. In embodiments, when R2 is substituted, it is substituted with at least one substituent group. In embodiments, when R2 is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when R2 is substituted, it is substituted with at least one lower substituent group.
In embodiments, L3 is a bond, —S(O)2—, —NR3—, —NH—, —O—, —S—, —C(O)—, —C(O)NR3—, —NR3C(O)—, —N(R3)CH2—, —NR3C(O)NH —, —NHC(O)NR3—, —C(O)O—, —OC(O)—, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted C1-C6 alkylene, or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted 2 to 6 membered heteroalkylene.
In embodiments, L3 is a bond, —S(O)2—, —NR3—, —NH—, —O—, —S—, —C(O)—, —C(O)NR3—, —NR3C(O)—, —N(R3)CH2—, —NR3C(O)NH —, —NHC(O)NR3—, —C(O)O—, —OC(O)—, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted alkylene (e.g., C1-C10, C1-C8, C1-C6, C1-C4, C1-C2, C2-C10, C2-C8, C2-C6, or C2-C4), or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroalkylene (e.g., 2 to 8 membered, 2 to 6 membered, 4 to 6 membered, 2 to 3 membered, or 4 to 5 membered).
In embodiments, a substituted L3 (e.g., substituted alkylene, substituted heteroalkylene, substituted cycloalkylene, substituted heterocycloalkylene, substituted arylene, and/or substituted heteroarylene) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted L3 is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different. In embodiments, when L3 is substituted, it is substituted with at least one substituent group. In embodiments, when L3 is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when L3 is substituted, it is substituted with at least one lower substituent group.
In embodiments, L4 is a bond, —NH—, —NR4—, or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted alkylene (e.g., C1-C10, C1-C8, C1-C6, C1-C4, C1-C2, C2-C10, C2-C8, C2-C6, or C2-C4).
In embodiments, a substituted L4 (e.g., substituted alkylene, substituted heteroalkylene, substituted cycloalkylene, substituted heterocycloalkylene, substituted arylene, and/or substituted heteroarylene) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted L4 is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different. In embodiments, when L4 is substituted, it is substituted with at least one substituent group. In embodiments, when L4 is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when L4 is substituted, it is substituted with at least one lower substituent group.
In embodiments, R16 is independently hydrogen, oxo, halogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —C(O)N(CH3)2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, —N3, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted alkyl (e.g., C1-C8, C1-C6, C1-C4, or C1-C2), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroalkyl (e.g., 2 to 8 membered, 2 to 6 membered, 4 to 6 membered, 2 to 3 membered, or 4 to 5 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted cycloalkyl (e.g., C3-C8, C3-C6, C4-C6, or C5-C6), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered, 3 to 6 membered, 4 to 6 membered, 4 to 5 membered, or 5 to 6 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted aryl (e.g., C6-C10 or phenyl), or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroaryl (e.g., 5 to 10 membered, 5 to 9 membered, or 5 to 6 membered).
In embodiments, R17 is independently hydrogen, oxo, halogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —C(O)N(CH3)2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, —N3, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted alkyl (e.g., C1-C8, C1-C6, C1-C4, or C1-C2), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroalkyl (e.g., 2 to 8 membered, 2 to 6 membered, 4 to 6 membered, 2 to 3 membered, or 4 to 5 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted cycloalkyl (e.g., C3-C8, C3-C6, C4-C6, or C5-C6), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered, 3 to 6 membered, 4 to 6 membered, 4 to 5 membered, or 5 to 6 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted aryl (e.g., C6-C10 or phenyl), or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroaryl (e.g., 5 to 10 membered, 5 to 9 membered, or 5 to 6 membered).
In embodiments, R18 is independently hydrogen, oxo, halogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —C(O)N(CH3)2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, —N3, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted alkyl (e.g., C1-C8, C1-C6, C1-C4, or C1-C2), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroalkyl (e.g., 2 to 8 membered, 2 to 6 membered, 4 to 6 membered , 2 to 3 membered, or 4 to 5 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted cycloalkyl (e.g., C3-C8, C3-C6, C4-C6, or C5-C6), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered, 3 to 6 membered, 4 to 6 membered, 4 to 5 membered, or 5 to 6 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted aryl (e.g., C6-C10 or phenyl), or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroaryl (e.g., 5 to 10 membered, 5 to 9 membered, or 5 to 6 membered).
In embodiments, R16, R17, and R18 are independently hydrogen, oxo, halogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —C(O)N(CH3)2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, —N3, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted C1-C6 alkyl, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted 2 to 6 membered heteroalkyl, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted C3-C6 cycloalkyl, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted 3 to 6 membered heterocycloalkyl, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted C6-C12 aryl, or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted 5 to 12 membered heteroaryl.
In embodiments, a substituted R16 (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R16 is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different. In embodiments, when R16 is substituted, it is substituted with at least one substituent group. In embodiments, when R16 is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when R16 is substituted, it is substituted with at least one lower substituent group.
In embodiments, a substituted R17 (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R17 is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different. In embodiments, when R17 is substituted, it is substituted with at least one substituent group. In embodiments, when R17 is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when R17 is substituted, it is substituted with at least one lower substituent group.
In embodiments, a substituted R18 (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R18 is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different. In embodiments, when R18 is substituted, it is substituted with at least one substituent group. In embodiments, when R18 is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when R18 is substituted, it is substituted with at least one lower substituent group.
In embodiments, R19 is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —COOH, —CONH2, —C(O)N(CH3)2, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted alkyl (e.g., C1-C8, C1-C6, C1-C4, or C1-C2), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroalkyl (e.g., 2 to 8 membered, 2 to 6 membered, 4 to 6 membered, 2 to 3 membered, or 4 to 5 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted cycloalkyl (e.g., C3-C8, C3-C6, C4-C6, or C5-C6), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered, 3 to 6 membered, 4 to 6 membered, 4 to 5 membered, or 5 to 6 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted aryl (e.g., C6-C10 or phenyl), or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroaryl (e.g., 5 to 10 membered, 5 to 9 membered, or 5 to 6 membered).
In embodiments, R20 is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —COOH, —CONH2, —C(O)N(CH3)2, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted alkyl (e.g., C1-C8, C1-C6, C1-C4, or C1-C2), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroalkyl (e.g., 2 to 8 membered, 2 to 6 membered, 4 to 6 membered, 2 to 3 membered, or 4 to 5 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted cycloalkyl (e.g., C3-C8, C3-C6, C4-C6, or C5-C6), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered, 3 to 6 membered, 4 to 6 membered, 4 to 5 membered, or 5 to 6 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted aryl (e.g., C6-C10 or phenyl), or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroaryl (e.g., 5 to 10 membered, 5 to 9 membered, or 5 to 6 membered).
In embodiments, a substituted R19 (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R19 is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different. In embodiments, when R19 is substituted, it is substituted with at least one substituent group. In embodiments, when R19 is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when R19 is substituted, it is substituted with at least one lower substituent group.
In embodiments, a substituted R20 (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R20 is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different. In embodiments, when R20 is substituted, it is substituted with at least one substituent group. In embodiments, when R20 is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when R20 is substituted, it is substituted with at least one lower substituent group.
In embodiments, R1A, R1B, R1C, R1D, R2A, R2B, R2C, and R2D are independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted alkyl, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroalkyl, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted cycloalkyl, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heterocycloalkyl, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted aryl, or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroaryl; R1A and R1B substituents bonded to the same nitrogen atom may optionally be joined to form a substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heterocycloalkyl or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroaryl; R2A and R2B substituents bonded to the same nitrogen atom may optionally be joined to form a substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heterocycloalkyl or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroaryl.
In embodiments, R1A is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted alkyl (e.g., C1-C8, C1-C6, C1-C4, or C1-C2), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroalkyl (e.g., 2 to 8 membered, 2 to 6 membered, 4 to 6 membered, 2 to 3 membered, or 4 to 5 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted cycloalkyl (e.g., C3-C8, C3-C6, C4-C6, or C5-C6), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered, 3 to 6 membered, 4 to 6 membered, 4 to 5 membered, or 5 to 6 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted aryl (e.g., C6-C10 or phenyl), or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroaryl (e.g., 5 to 10 membered, 5 to 9 membered, or 5 to 6 membered).
In embodiments, a substituted R1A (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R1A is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different. In embodiments, when R1A is substituted, it is substituted with at least one substituent group. In embodiments, when R1A is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when R1A is substituted, it is substituted with at least one lower substituent group.
In embodiments, R1B is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted alkyl (e.g., C1-C8, C1-C6, C1-C4, or C1-C2), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroalkyl (e.g., 2 to 8 membered, 2 to 6 membered, 4 to 6 membered, 2 to 3 membered, or 4 to 5 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted cycloalkyl (e.g., C3-C8, C3-C6, C4-C6, or C5-C6), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered, 3 to 6 membered, 4 to 6 membered, 4 to 5 membered, or 5 to 6 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted aryl (e.g., C6-C10 or phenyl), or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroaryl (e.g., 5 to 10 membered, 5 to 9 membered, or 5 to 6 membered).
In embodiments, a substituted R1B (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R1B is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different. In embodiments, when R1B is substituted, it is substituted with at least one substituent group. In embodiments, when R1B is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when R1B is substituted, it is substituted with at least one lower substituent group.
In embodiments, R1C is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted alkyl (e.g., C1-C8, C1-C6, C1-C4, or C1-C2), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroalkyl (e.g., 2 to 8 membered, 2 to 6 membered, 4 to 6 membered, 2 to 3 membered, or 4 to 5 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted cycloalkyl (e.g., C3-C8, C3-C6, C4-C6, or C5-C6), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered, 3 to 6 membered, 4 to 6 membered, 4 to 5 membered, or 5 to 6 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted aryl (e.g., C6-C10 or phenyl), or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroaryl (e.g., 5 to 10 membered, 5 to 9 membered, or 5 to 6 membered).
In embodiments, a substituted R1C (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R1C is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different. In embodiments, when R1C is substituted, it is substituted with at least one substituent group. In embodiments, when R1C is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when R1C is substituted, it is substituted with at least one lower substituent group.
In embodiments, R1D is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted alkyl (e.g., C1-C8, C1-C6, C1-C4, or C1-C2), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroalkyl (e.g., 2 to 8 membered, 2 to 6 membered, 4 to 6 membered, 2 to 3 membered, or 4 to 5 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted cycloalkyl (e.g., C3-C8, C3-C6, C4-C6, or C5-C6), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered, 3 to 6 membered, 4 to 6 membered, 4 to 5 membered, or 5 to 6 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted aryl (e.g., C6-C10 or phenyl), or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroaryl (e.g., 5 to 10 membered, 5 to 9 membered, or 5 to 6 membered).
In embodiments, a substituted R1D (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R1D is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different. In embodiments, when R1D is substituted, it is substituted with at least one substituent group. In embodiments, when R1D is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when R1D is substituted, it is substituted with at least one lower substituent group.
In embodiments, R1A and R1B substituents bonded to the same nitrogen atom may optionally be joined to form a substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered, 3 to 6 membered, 4 to 6 membered, 4 to 5 membered, or 5 to 6 membered) or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroaryl (e.g., 5 to 10 membered, 5 to 9 membered, or 5 to 6 membered).
In embodiments, R1A and R1B substituents bonded to the same nitrogen atom that are optionally joined to form a substituted heterocycloalkyl can be substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted heterocycloalkyl is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different. In embodiments, when the substituted heterocycloalkyl is substituted, it is substituted with at least one substituent group. In embodiments, when the substituted heterocycloalkyl is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when the substituted heterocycloalkyl is substituted, it is substituted with at least one lower substituent group.
In embodiments, R2A is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted alkyl (e.g., C1-C8, C1-C6, C1-C4, or C1-C2), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroalkyl (e.g., 2 to 8 membered, 2 to 6 membered, 4 to 6 membered , 2 to 3 membered, or 4 to 5 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted cycloalkyl (e.g., C3-C8, C3-C6, C4-C6, or C5-C6), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered, 3 to 6 membered, 4 to 6 membered, 4 to 5 membered, or 5 to 6 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted aryl (e.g., C6-C10 or phenyl), or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroaryl (e.g., 5 to 10 membered, 5 to 9 membered, or 5 to 6 membered).
In embodiments, a substituted R2A (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R2A is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different. In embodiments, when R2A is substituted, it is substituted with at least one substituent group. In embodiments, when R2A is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when R2A is substituted, it is substituted with at least one lower substituent group.
In embodiments, R2B is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted alkyl (e.g., C1-C8, C1-C6, C1-C4, or C1-C2), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroalkyl (e.g., 2 to 8 membered, 2 to 6 membered, 4 to 6 membered, 2 to 3 membered, or 4 to 5 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted cycloalkyl (e.g., C3-C8, C3-C6, C4-C6, or C5-C6), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered, 3 to 6 membered, 4 to 6 membered, 4 to 5 membered, or 5 to 6 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted aryl (e.g., C6-C10 or phenyl), or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroaryl (e.g., 5 to 10 membered, 5 to 9 membered, or 5 to 6 membered).
In embodiments, a substituted R2B (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R2B is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different. In embodiments, when R2B is substituted, it is substituted with at least one substituent group. In embodiments, when R2B is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when R2B is substituted, it is substituted with at least one lower substituent group.
In embodiments, R2C is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted alkyl (e.g., C1-C8, C1-C6, C1-C4, or C1-C2), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroalkyl (e.g., 2 to 8 membered, 2 to 6 membered, 4 to 6 membered, 2 to 3 membered, or 4 to 5 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted cycloalkyl (e.g., C3-C8, C3-C6, C4-C6, or C5-C6), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered, 3 to 6 membered, 4 to 6 membered, 4 to 5 membered, or 5 to 6 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted aryl (e.g., C6-C10 or phenyl), or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroaryl (e.g., 5 to 10 membered, 5 to 9 membered, or 5 to 6 membered).
In embodiments, a substituted R2C (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R2C is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different. In embodiments, when R2C is substituted, it is substituted with at least one substituent group. In embodiments, when R2C is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when R2C is substituted, it is substituted with at least one lower substituent group.
In embodiments, R2D is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted alkyl (e.g., C1-C8, C1-C6, C1-C4, or C1-C2), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroalkyl (e.g., 2 to 8 membered, 2 to 6 membered, 4 to 6 membered, 2 to 3 membered, or 4 to 5 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted cycloalkyl (e.g., C3-C8, C3-C6, C4-C6, or C5-C6), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered, 3 to 6 membered, 4 to 6 membered, 4 to 5 membered, or 5 to 6 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted aryl (e.g., C6-C10 or phenyl), or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroaryl (e.g., 5 to 10 membered, 5 to 9 membered, or 5 to 6 membered).
In embodiments, a substituted R2D (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R2D is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different. In embodiments, when R2D is substituted, it is substituted with at least one substituent group. In embodiments, when R2D is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when R2D is substituted, it is substituted with at least one lower substituent group.
In embodiments, R2A and R2B substituents bonded to the same nitrogen atom may optionally be joined to form a substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered, 3 to 6 membered, 4 to 6 membered, 4 to 5 membered, or 5 to 6 membered) or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroaryl (e.g., 5 to 10 membered, 5 to 9 membered, or 5 to 6 membered).
In embodiments, R2A and R2B substituents bonded to the same nitrogen atom that are optionally joined to form a substituted heterocycloalkyl can be substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted heterocycloalkyl is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different. In embodiments, when the substituted heterocycloalkyl is substituted, it is substituted with at least one substituent group. In embodiments, when the substituted heterocycloalkyl is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when the substituted heterocycloalkyl is substituted, it is substituted with at least one lower substituent group.
In embodiments, R1.2 is independently hydrogen, halogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, —N3, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted alkyl (e.g., C1-C8, C1-C6, C1-C4, or C1-C2), or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroalkyl (e.g., 2 to 8 membered, 2 to 6 membered, 4 to 6 membered, 2 to 3 membered, or 4 to 5 membered).
In embodiments, R1.3 is independently hydrogen, halogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, —N3, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted alkyl (e.g., C1-C8, C1-C6, C1-C4, or C1-C2), or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroalkyl (e.g., 2 to 8 membered, 2 to 6 membered, 4 to 6 membered, 2 to 3 membered, or 4 to 5 membered).
In embodiments, R1.2 and R1.3 substituents on adjacent carbons may optionally be joined to form a substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted phenyl, or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted 5 to 6 membered heteroaryl.
In embodiments, R1.2 and R1.3 are independently hydrogen, halogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, —N3, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted C1-C6 alkyl, or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted 2 to 6 membered heteroalkyl; or R1.2 and R1.3 substituents on adjacent carbons may optionally be joined to form a substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted phenyl, or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted 5 to 6 membered heteroaryl.
In embodiments, a substituted R1.2 (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R1.2 is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different. In embodiments, when R1.2 is substituted, it is substituted with at least one substituent group. In embodiments, when R1.2 is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when R1.2 is substituted, it is substituted with at least one lower substituent group.
In embodiments, a substituted R1.3 (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R1.3 is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different. In embodiments, when R1.3 is substituted, it is substituted with at least one substituent group. In embodiments, when R1.3 is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when R1.3 is substituted, it is substituted with at least one lower substituent group.
In embodiments, R1.2 and R1.3 substituents on adjacent carbons may optionally be joined to form a substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted aryl (e.g., C6-C10 or phenyl), or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroaryl (e.g., 5 to 10 membered, 5 to 9 membered, or 5 to 6 membered).
In embodiments, R1.4 is independently hydrogen, halogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, —N3, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted alkyl (e.g., C1-C8, C1-C6, C1-C4, or C1-C2), or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroalkyl (e.g., 2 to 8 membered, 2 to 6 membered, 4 to 6 membered, 2 to 3 membered, or 4 to 5 membered).
In embodiments, R1.5 is independently hydrogen, halogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, —N3, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted alkyl (e.g., C1-C8, C1-C6, C1-C4, or C1-C2), or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroalkyl (e.g., 2 to 8 membered, 2 to 6 membered, 4 to 6 membered, 2 to 3 membered, or 4 to 5 membered).
In embodiments, R1.4 and R1.5 are independently hydrogen, halogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, —N3, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted C1-C6 alkyl, or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted 2 to 6 membered heteroalkyl.
In embodiments, a substituted R1.4 (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R1.4 is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different. In embodiments, when R1.4 is substituted, it is substituted with at least one substituent group. In embodiments, when R1.4 is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when R1.4 is substituted, it is substituted with at least one lower substituent group.
In embodiments, a substituted R1.5 (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R1.5 is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different. In embodiments, when R1.5 is substituted, it is substituted with at least one substituent group. In embodiments, when R1.5 is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when R1.5 is substituted, it is substituted with at least one lower substituent group.
In embodiments, R2.1 is independently oxo, halogen, —CX23, —CHX22, —CH2X2, —OCX23, —OCH2X2, —OCHX22, —CN, —SOn2R2D, —SOv2NR2AR2B, —NR2CNR2AR2B, —ONR2AR2B, —NHC(O)NR2CNR2AR2B,—NHC(O)NR2AR2B, —N(O)m2, —NR2AR2B, —C(O)R2C, —C(O)—OR2C, —C(O) NR2AR2B, —OR2D, —NR2ASO2R2D, —NR2AC(O)R2C, —NR2AC(O)OR2C, —NR2AOR2C, —SF5, —N3, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted alkyl (e.g., C1-C8, C1-C6, C1-C4, or C1-C2), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroalkyl (e.g., 2 to 8 membered, 2 to 6 membered, 4 to 6 membered, 2 to 3 membered, or 4 to 5 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted cycloalkyl (e.g., C3-C8, C3-C6, C4-C6, or C5-C6), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered, 3 to 6 membered, 4 to 6 membered, 4 to 5 membered, or 5 to 6 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted aryl (e.g., C6-C10 or phenyl), or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroaryl (e.g., 5 to 10 membered, 5 to 9 membered, or 5 to 6 membered).
In embodiments, a substituted R2.1 (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R2.1 is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different. In embodiments, when R2.1 is substituted, it is substituted with at least one substituent group. In embodiments, when R2.1 is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when R2.1 is substituted, it is substituted with at least one lower substituent group.
In embodiments, R2.2 is independently oxo, halogen, —CX23, —CHX22, —CH2X2, —OCX23, —OCH2X2, —OCHX22, —CN, —SOn2R2D, —SOv2NR2AR2B, —NR2CNR2AR2B, —ONR2AR2B, —NHC(O)NR2CNR2AR2B,—NHC(O)NR2AR2B, —N(O)m2, —NR2AR2B, —C(O)R2C, —C(O)—OR2C, —C(O) NR2AR2B, —OR2D, —NR2ASO2R2D, —NR2AC(O)R2C, —NR2AC(O)OR2C, —NR2AOR2C, —SF5, —N3, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted alkyl (e.g., C1-C8, C1-C6, C1-C4, or C1-C2), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroalkyl (e.g., 2 to 8 membered, 2 to 6 membered, 4 to 6 membered, 2 to 3 membered, or 4 to 5 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted cycloalkyl (e.g., C3-C8, C3-C6, C4-C6, or C5-C6), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered, 3 to 6 membered, 4 to 6 membered, 4 to 5 membered, or 5 to 6 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted aryl (e.g., C6-C10 or phenyl), or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroaryl (e.g., 5 to 10 membered, 5 to 9 membered, or 5 to 6 membered).
In embodiments, a substituted R2.2 (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R2.2 is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different. In embodiments, when R2.2 is substituted, it is substituted with at least one substituent group. In embodiments, when R2.2 is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when R2.2 is substituted, it is substituted with at least one lower substituent group.
In embodiments, R1 is independently halogen, —CX13, —CHX12, —CH2X1, —OCX13, —OCH2X1, —OCHX12, —CN, —SOn1R1D, —SOv1NR1AR1B, —NR1CNR1AR1B, —ONR1AR1B, —NHC(O)NR1CNR1AR1B, —NHC(O)NR1AR1B, —N(O)m1, —NR1AR1B, —C(O)R1C, —C(O)—OR1C, —C(O) NR1AR1B, —OR1D, —NR1ASO2R1D, —NR1AC(O)R1C, —NR1AC(O)OR1C, —NR1AOR1C, —SF5, —N3, R11-substituted or unsubstituted alkyl, R11-substituted or unsubstituted heteroalkyl, R11-substituted or unsubstituted cycloalkyl, R11-substituted or unsubstituted heterocycloalkyl, R11-substituted or unsubstituted aryl, or R11-substituted or unsubstituted heteroaryl; two adjacent R1 substituents on adjacent carbons may optionally be joined to form a R11-substituted or unsubstituted cycloalkyl, R11-substituted or unsubstituted heterocycloalkyl, R11-substituted or unsubstituted aryl, or R11-substituted or unsubstituted heteroaryl.
In embodiments, R1 is independently halogen, —CX13, —CHX12, —CH2X1, —OCX13, —OCH2X1, —OCHX12, —CN, —SOn1R1D, —SOv1NR1AR1B, —NR1CNR1AR1B, —ONR1AR1B, —NHC(O)NR1CNR1AR1B, —NHC(O)NR1AR1B, —N(O)m1, —NR1AR1B, —C(O)R1C, —C(O)—OR1C, —C(O) NR1AR1B, —OR1D, —NR1ASO2R1D, —NR1AC(O)R1C, —NR1AC(O)OR1C, —NR1AOR1C, —SF5, —N3, R11-substituted or unsubstituted C1-C6 alkyl, R11-substituted or unsubstituted 2 to 6 membered heteroalkyl, R11-substituted or unsubstituted C3-C6 cycloalkyl, R11-substituted or unsubstituted 3 to 6 membered heterocycloalkyl, R11-substituted or unsubstituted C6-C10 aryl, or R11-substituted or unsubstituted 5 to 10 membered heteroaryl; two adjacent R1 substituents on adjacent carbons may optionally be joined to form a R11-substituted or unsubstituted C3-C6 cycloalkyl, R11-substituted or unsubstituted 3 to 6 membered heterocycloalkyl, R11-substituted or unsubstituted phenyl, or R11-substituted or unsubstituted 5 to 6 membered heteroaryl.
In embodiments, R1.2 and R1.3 are independently hydrogen, halogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, —N3, R11-substituted or unsubstituted C1-C6 alkyl, or R11-substituted or unsubstituted 2 to 6 membered heteroalkyl; or R1.2 and R1.3 substituents on adjacent carbons may optionally be joined to form a R11-substituted or unsubstituted phenyl, or R11-substituted or unsubstituted 5 to 6 membered heteroaryl.
In embodiments, R1.2 is independently hydrogen, halogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, —N3, R11-substituted or unsubstituted C1-C6 alkyl, or R11-substituted or unsubstituted 2 to 6 membered heteroalkyl.
In embodiments, R1.3 is independently hydrogen, halogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, —N3, R11-substituted or unsubstituted C1-C6 alkyl, or R11-substituted or unsubstituted 2 to 6 membered heteroalkyl.
In embodiments, R1.2 and R1.3 substituents on adjacent carbons may optionally be joined to form a R11-substituted or unsubstituted phenyl, or R11-substituted or unsubstituted 5 to 6 membered heteroaryl.
In embodiments, R1.4 and R1.5 are independently hydrogen, halogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, —N3, R11-substituted or unsubstituted C1-C6 alkyl, or R11-substituted or unsubstituted 2 to 6 membered heteroalkyl.
In embodiments, R1.4 is independently hydrogen, halogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, —N3, R11-substituted or unsubstituted C1-C6 alkyl, or R11-substituted or unsubstituted 2 to 6 membered heteroalkyl.
In embodiments, R1.5 is independently hydrogen, halogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl3, —OCF3, —OCBr3, —OCI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, —N3, R11-substituted or unsubstituted C1-C6 alkyl, or R11-substituted or unsubstituted 2 to 6 membered heteroalkyl.
In embodiments, R1A, R1B, R1C, and R1D independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, R11-substituted or unsubstituted alkyl, R11-substituted or unsubstituted heteroalkyl, R11-substituted or unsubstituted cycloalkyl, R11-substituted or unsubstituted heterocycloalkyl, R11-substituted or unsubstituted aryl, or R11-substituted or unsubstituted heteroaryl; R1A and R1B substituents bonded to the same nitrogen atom may optionally be joined to form a R11-substituted or unsubstituted heterocycloalkyl or R11-substituted or unsubstituted heteroaryl.
In embodiments, R1A is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, R11-substituted or unsubstituted alkyl, R11-substituted or unsubstituted heteroalkyl, R11-substituted or unsubstituted cycloalkyl, R11-substituted or unsubstituted heterocycloalkyl, R11-substituted or unsubstituted aryl, or R11-substituted or unsubstituted heteroaryl.
In embodiments, R1B is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, R11-substituted or unsubstituted alkyl, R11-substituted or unsubstituted heteroalkyl, R11-substituted or unsubstituted cycloalkyl, R11-substituted or unsubstituted heterocycloalkyl, R11-substituted or unsubstituted aryl, or R11-substituted or unsubstituted heteroaryl.
In embodiments, R1A and R1B substituents bonded to the same nitrogen atom may optionally be joined to form a R11-substituted or unsubstituted heterocycloalkyl or R11-substituted or unsubstituted heteroaryl.
In embodiments, R1C is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, R11-substituted or unsubstituted alkyl, R11-substituted or unsubstituted heteroalkyl, R11 -substituted or unsubstituted cycloalkyl, R11-substituted or unsubstituted heterocycloalkyl, R11-substituted or unsubstituted aryl, or R11-substituted or unsubstituted heteroaryl.
In embodiments, R1D is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, R11-substituted or unsubstituted alkyl, R11-substituted or unsubstituted heteroalkyl, R11-substituted or unsubstituted cycloalkyl, R11-substituted or unsubstituted heterocycloalkyl, R11-substituted or unsubstituted aryl, or R11-substituted or unsubstituted heteroaryl.[0487] In embodiments, R2 is independently oxo, halogen, —CX23, —CHX22, —CH2X2, —OCX23, —OCH2X2, —OCHX22, —CN, —SOn2R2D, —SOv2NR2AR2B, —NR2CNR2AR2B, —ONR2AR2B, —NHC(O)NR2CNR2AR2B,—NHC(O)NR2AR2B, —N(O)m2, —NR2AR2B, —C(O)R2C, —C(O)—OR2C, —C(O) NR2AR2B, —OR2D, —NR2ASO2R2D, —NR2AC(O)R2C, —NR2AC(O)OR2C, —NR2AOR2C, —SF5, —N3, R21-substituted or unsubstituted C1-C6 alkyl, R21-substituted or unsubstituted 2 to 6 membered heteroalkyl, R21-substituted or unsubstituted C3-C6 cycloalkyl, R21-substituted or unsubstituted 3 to 6 membered heterocycloalkyl, R21-substituted or unsubstituted C6-C10 aryl, or R21-substituted or unsubstituted 5 to 10 membered heteroaryl.
In embodiments, R2A, R2B, R2C, and R2D are independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, R21-substituted or unsubstituted alkyl, R21-substituted or unsubstituted heteroalkyl, R21-substituted or unsubstituted cycloalkyl, R21-substituted or unsubstituted heterocycloalkyl, R21-substituted or unsubstituted aryl, or R21-substituted or unsubstituted heteroaryl; R2A and R2B substituents bonded to the same nitrogen atom may optionally be joined to form a R21-substituted or unsubstituted heterocycloalkyl or R21-substituted or unsubstituted heteroaryl.
In embodiments, R2A is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, R21-substituted or unsubstituted alkyl, R21-substituted or unsubstituted heteroalkyl, R21-substituted or unsubstituted cycloalkyl, R21-substituted or unsubstituted heterocycloalkyl, R21-substituted or unsubstituted aryl, or R21-substituted or unsubstituted heteroaryl.
In embodiments, R2B is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, R21-substituted or unsubstituted alkyl, R21-substituted or unsubstituted heteroalkyl, R21-substituted or unsubstituted cycloalkyl, R21-substituted or unsubstituted heterocycloalkyl, R21-substituted or unsubstituted aryl, or R21-substituted or unsubstituted heteroaryl.
In embodiments, R2A and R2B substituents bonded to the same nitrogen atom may optionally be joined to form a R21-substituted or unsubstituted heterocycloalkyl or R21-substituted or unsubstituted heteroaryl.
In embodiments, R2C is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, R21-substituted or unsubstituted alkyl, R21-substituted or unsubstituted heteroalkyl, R21-substituted or unsubstituted cycloalkyl, R21-substituted or unsubstituted heterocycloalkyl, R21-substituted or unsubstituted aryl, or R21-substituted or unsubstituted heteroaryl.
In embodiments, R2D is independently hydrogen, —CCl3, —CBr3, —CF3, —CI3, CHCl2, —CHBr2, —CHF2, —CHI2, —CH2Cl, —CH2Br, —CH2F, —CH2I, —CN, —OH, —NH2, —COOH, —CONH2, —OCCl3, —OCF3, —OCBr3, —O CI3, —OCHCl2, —OCHBr2, —OCHI2, —OCHF2, —OCH2Cl, —OCH2Br, —OCH2I, —OCH2F, R21-substituted or unsubstituted alkyl, R21-substituted or unsubstituted heteroalkyl, R21-substituted or unsubstituted cycloalkyl, R21-substituted or unsubstituted heterocycloalkyl, R21-substituted or unsubstituted aryl, or R21-substituted or unsubstituted heteroaryl.
In embodiments, R11 is independently oxo, halogen, -CX113, -CHX112, —CH2X11, —OCX113, —OCH2X11, —OCHX112, —CN, —OH, —NH2, —COOH, —CONH2, —C(O)N(CH3)2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —N3, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted alkyl (e.g., C1-C8, C1-C6, C1-C4, or C1-C2), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroalkyl (e.g., 2 to 8 membered, 2 to 6 membered, 4 to 6 membered, 2 to 3 membered, or 4 to 5 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted cycloalkyl (e.g., C3-C8, C3-C6, C4-C6, or C5-C6), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered, 3 to 6 membered, 4 to 6 membered, 4 to 5 membered, or 5 to 6 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted aryl (e.g., C6-C10 or phenyl), or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroaryl (e.g., 5 to 10 membered, 5 to 9 membered, or 5 to 6 membered).
In embodiments, a substituted R11 (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R11 is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different. In embodiments, when R11 is substituted, it is substituted with at least one substituent group. In embodiments, when R11 is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when R11 is substituted, it is substituted with at least one lower substituent group.
In embodiments, R21 is independently oxo, halogen, -CX213, -CHX212, —CH2X21, —OCX213, —OCH2X21, —OCHX212, —CN, —OH, —NH2, —COOH, —CONH2, —C(O)N(CH3)2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —N3, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted alkyl (e.g., C1-C8, C1-C6, C1-C4, or C1-C2), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroalkyl (e.g., 2 to 8 membered, 2 to 6 membered, 4 to 6 membered, 2 to 3 membered, or 4 to 5 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted cycloalkyl (e.g., C3-C8, C3-C6, C4-C6, or C5-C6), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered, 3 to 6 membered, 4 to 6 membered, 4 to 5 membered, or 5 to 6 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted aryl (e.g., C6-C10 or phenyl), or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroaryl (e.g., 5 to 10 membered, 5 to 9 membered, or 5 to 6 membered).
In embodiments, a substituted R21 (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R21 is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different. In embodiments, when R21 is substituted, it is substituted with at least one substituent group. In embodiments, when R21 is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when R21 is substituted, it is substituted with at least one lower substituent group.
In embodiments, R11.1 is independently oxo, halogen, -CX113, -CHX112, —CH2X11, —OCX113, —OCH2X11, —OCHX112, —CN, —OH, —NH2, —COOH, —CONH2, —C(O)N(CH3)2, —NO2, —SH, —SO3H, —SO4H, —SO2NH2, —NHNH2, —ONH2, —NHC(O)NHNH2, —NHC(O)NH2, —NHSO2H, —NHC(O)H, —NHC(O)OH, —NHOH, —N3, substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted alkyl (e.g., C1-C8, C1-C6, C1-C4, or C1-C2), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroalkyl (e.g., 2 to 8 membered, 2 to 6 membered, 4 to 6 membered, 2 to 3 membered, or 4 to 5 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted cycloalkyl (e.g., C3-C8, C3-C6, C4-C6, or C5-C6), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heterocycloalkyl (e.g., 3 to 8 membered, 3 to 6 membered, 4 to 6 membered, 4 to 5 membered, or 5 to 6 membered), substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted aryl (e.g., C6-C10 or phenyl), or substituted (e.g., substituted with at least one substituent group, size-limited substituent group, or lower substituent group) or unsubstituted heteroaryl (e.g., 5 to 10 membered, 5 to 9 membered, or 5 to 6 membered).
In embodiments, a substituted R11.1 (e.g., substituted alkyl, substituted heteroalkyl, substituted cycloalkyl, substituted heterocycloalkyl, substituted aryl, and/or substituted heteroaryl) is substituted with at least one substituent group, size-limited substituent group, or lower substituent group; wherein if the substituted R11.1 is substituted with a plurality of groups selected from substituent groups, size-limited substituent groups, and lower substituent groups; each substituent group, size-limited substituent group, and/or lower substituent group may optionally be different. In embodiments, when R 11.1 is substituted, it is substituted with at least one substituent group. In embodiments, when R11.1 is substituted, it is substituted with at least one size-limited substituent group. In embodiments, when R11.1 is substituted, it is substituted with at least one lower substituent group.
In embodiments, the compound has the formula:
R17 is substituted or unsubstituted aryl; and R15, R16, and R18 are as described herein, including embodiments. In embodiments, R17 is substituted or unsubstituted phenyl. In embodiments, the compound has the formula:
R17 is substituted or unsubstituted aryl; and R14, R16, and R18 are as described herein, including embodiments. In embodiments, R17 is substituted or unsubstituted phenyl. In embodiments, the compound has the formula:
R17 is substituted or unsubstituted aryl; and R16, and R18 are as described herein, including embodiments. In embodiments, R17 is substituted or unsubstituted phenyl. In embodiments, the compound has the formula:
R17 is substituted or unsubstituted aryl; and R14, R15, R16, and R18 are as described herein, including embodiments. In embodiments, R17 is substituted or unsubstituted phenyl. In embodiments, the compound has the formula:
R17 is substituted or unsubstituted aryl; and R15 is as described herein, including embodiments. In embodiments, R17 is substituted or unsubstituted phenyl. In embodiments, the compound has the formula:
R17 is substituted or unsubstituted aryl; and R14 is as described herein, including embodiments. In embodiments, R17 is substituted or unsubstituted phenyl. In embodiments, the compound has the formula:
R17 is substituted or unsubstituted aryl. In embodiments, R17 is substituted or unsubstituted phenyl. In embodiments, the compound has the formula:
R17 is substituted or unsubstituted aryl; and R14 and R15 are as described herein, including embodiments. In embodiments, R17 is substituted or unsubstituted phenyl. In embodiments, the compound has the formula:
R17 is substituted or unsubstituted aryl; and R15, R16, and R18 are as described herein, including embodiments. In embodiments, R17 is substituted or unsubstituted phenyl. In embodiments, the compound has the formula:
R17 is substituted or unsubstituted aryl; and R14, R16, and R18 are as described herein, including embodiments. In embodiments, R17 is substituted or unsubstituted phenyl. In embodiments, the compound has the formula:
R17 is substituted or unsubstituted aryl; and R16, and R18 are as described herein, including embodiments. In embodiments, R17 is substituted or unsubstituted phenyl. In embodiments, the compound has the formula:
R17 is substituted or unsubstituted aryl; and R14, R15, R16, and R18 are as described herein, including embodiments. In embodiments, R17 is substituted or unsubstituted phenyl. In embodiments, the compound has the formula:
R17 is substituted or unsubstituted aryl; and R15 is as described herein, including embodiments. In embodiments, R17 is substituted or unsubstituted phenyl. In embodiments, the compound has the formula:
R17 is substituted or unsubstituted aryl; and R14 is as described herein, including embodiments. In embodiments, R17 is substituted or unsubstituted phenyl. In embodiments, the compound has the formula:
R17 is substituted or unsubstituted aryl. In embodiments, R17 is substituted or unsubstituted phenyl. In embodiments, the compound has the formula:
R17 is substituted or unsubstituted aryl; and R14 and R15 are as described herein, including embodiments. In embodiments, R17 is substituted or unsubstituted phenyl.
In embodiments, the compound has the formula:
R19 is hydrogen, —CH3, —CF3, or —CN; and R16, R17, and R18 are as described herein, including embodiments. In embodiments, the compound has the formula:
R19 is hydrogen, —CH3, —CF3, or —CN. In embodiments, the compound has the formula:
R19 is hydrogen, —CH3, —CF3, or —CN; and R16, R17, and R18 are as described herein, including embodiments. In embodiments, the compound has the formula:
R19 is hydrogen, —CH3, —CF3, or —CN.
In embodiments, the compound has the formula:
R19 and R20 are independently hydrogen, —CH3, —CF3, or —CN; and R16, R17, and R18 are as described herein, including embodiments. In embodiments, R19 is hydrogen or —CH3. In embodiments, R20 is hydrogen or —CH3. In embodiments, the compound has the formula:
R19 and R20 are independently hydrogen, —CH3, —CF3, or —CN. In embodiments, R19 is hydrogen or —CH3. In embodiments, R20 is hydrogen or —CH3. In embodiments, the compound has the formula:
R19 and R20 are independently hydrogen, —CH3, —CF3, or —CN; and R16, R17, and R18 are as described herein, including embodiments. In embodiments, R19 is hydrogen or —CH3. In embodiments, R20 is hydrogen or —CH3. In embodiments, the compound has the formula:
R19 and R20 are independently hydrogen, —CH3, —CF3, or —CN. In embodiments, R19 is hydrogen or —CH3. In embodiments, R20 is hydrogen or —CH3.
In embodiments, the compound has the formula:
R19 is hydrogen, —CH3, —CF3, or —CN; and R16, R17, and R18 are as described herein, including embodiments. In embodiments, the compound has the formula:
R19 is hydrogen, —CH3, —CF3, or —CN. In embodiments, the compound has the formula:
R19 is hydrogen, —CH3, —CF3, or —CN; and R16, R17, and R18 are as described herein, including embodiments. In embodiments, the compound has the formula:
R19 is hydrogen, —CH3, —CF3, or —CN.
In embodiments, the compound has the formula:
R6 is —CF3, —COCH3, or unsubstituted cyclopropyl; and R16, R17, and R18 are as described herein, including embodiments. In embodiments, the compound has the formula:
R6 is —CF3, —COCH3, or unsubstituted cyclopropyl. In embodiments, the compound has the formula:
R6 is —CF3, —COCH3, or unsubstituted cyclopropyl; and R16, R17, and R18 are as described herein, including embodiments. In embodiments, the compound has the formula:
R6 is —CF3, —COCH3, or unsubstituted cyclopropyl. In embodiments, the compound has the formula:
. R6 is —CF3, —COCH3, or unsubstituted cyclopropyl; and R16, R17, and R18 are as described herein, including embodiments. In embodiments, the compound has the formula: or unsubstituted cyclopropyl.
R6 is —CF3, —COCH3,
In embodiments, the compound is:
In embodiments, the compound is:
In embodiments, the compound is:
In embodiments, the compound is:
In embodiments, the compound is:
In embodiments, the compound is:
In embodiments, the compound is:
In embodiments, the compound is:
In embodiments, the compound is:
In embodiments, the compound is:
In embodiments, the compound is:
In embodiments, the compound
In embodiments, the compound is:
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In embodiments, the compound is:
In embodiments, the compound is:
In embodiments, the compound is:
In embodiments, the compound is:
In embodiments, the compound is:
In embodiments, the compound is:
In embodiments, the compound is:
In embodiments, the compound is:
In embodiments, the compound is:
[0508] In embodiments, the compound is:
In embodiments, the compound is:
In embodiments, the compound is:
In embodiments, the compound is:
In embodiments, the compound is:
In embodiments, the compound is:
In embodiments, the compound is useful as a comparator compound. In embodiments, the comparator compound can be used to assess the activity of a test compound in an assay (e.g., an assay as described herein, for example in the examples section, figures, or tables).
In embodiments, the compound is a compound described herein (e.g., in an aspect, embodiment, example, table, figure, or claim).
In an aspect is provided a pharmaceutical composition including a compound as described herein, including in embodiments, and a pharmaceutically acceptable excipient. In embodiments, the compound as described herein is included in a therapeutically effective amount.
In embodiments of the pharmaceutical compositions, the compound, or pharmaceutically acceptable salt thereof, is included in a therapeutically effective amount.
In embodiments of the pharmaceutical compositions, the pharmaceutical composition includes a second agent (e.g. therapeutic agent). In embodiments of the pharmaceutical compositions, the pharmaceutical composition includes a second agent (e.g. therapeutic agent) in a therapeutically effective amount. In embodiments of the pharmaceutical compositions, the second agent is an agent for treating a neurodegenerative disease. In embodiments of the pharmaceutical compositions, the second agent is an agent for treating Alzheimer’s disease, Huntington’s disease, Amyotrophic lateral sclerosis, Lewy body disease, Progressive Supranuclear Palsy, or Parkinson’s disease. In embodiments of the pharmaceutical compositions, the second agent is an agent for treating a liver disease. In embodiments of the pharmaceutical compositions, the second agent is an agent for treating nonalcoholic steatohepatitis or nonalcoholic fatty liver disease. In embodiments, the administering does not include administration of any active agent other than the recited active agent (e.g., a compound described herein).
In an aspect is provided a method of inhibiting human Caspase 6 protein activity, the method including: contacting the human Caspase 6 protein with a compound as described herein.
In embodiments, the compound covalently binds C264 of the human Caspase 6 protein. In embodiments, the compound covalently binds an amino acid corresponding to cysteine 264 of the human Caspase 6 protein. In embodiments, the compound forms a covalent bond with the protein. In embodiments, the compounds binds via an irreversible covalent bond.
In embodiments, the compound inhibits the activity of human Caspase 6 protein more than other human Caspase proteins.
In embodiments, the compound inhibits the activity of human Caspase 6 protein more than human Caspase 2 and human Caspase 3. In embodiments, the compound inhibits human Caspase 6 protein at least 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2, 3, 4, 5, 6, 7, 8, 9, 10, 20, 30, 40, 50, 60, 70, 80, 90, 100, 200, 300, 400, 500 600, 700, 800, 900, 1000, 2000, 3000, 4000, 5000, 6000, 7000, 8000, 9000, 10000, 20000, 30000, 40000, 50000, 60000, 70000, 80000, 90000, or 100000 fold more than human Caspase 2. In embodiments, the compound inhibits human Caspase 6 protein at least 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2, 3, 4, 5, 6, 7, 8, 9, 10, 20, 30, 40, 50, 60, 70, 80, 90, 100, 200, 300, 400, 500 600, 700, 800, 900, 1000, 2000, 3000, 4000, 5000, 6000, 7000, 8000, 9000, 10000, 20000, 30000, 40000, 50000, 60000, 70000, 80000, 90000, or 100000 fold more than human Caspase 3.
In an aspect is provided a method of treating a neurodegenerative disease, the method including administering to a subject in need thereof an effective amount of a compound as disclosed herein.
In embodiments, the neurodegenerative disease is a tauopathy.
In embodiments, the neurodegenerative disease is Alzheimer’s disease, Huntington’s disease, Amyotrophic lateral sclerosis, Lewy body disease, Progressive Supranuclear Palsy, Parkinson’s disease, frontotemporal degeneration (FTD), frontotemporal lobar degeneration (FTLD), or Pick’s disease.
In embodiments, the neurodegenerative disease is Alzheimer’s disease, Huntington’s disease, Amyotrophic lateral sclerosis, Lewy body disease, Progressive Supranuclear Palsy, or Parkinson’s disease.
In embodiments, the neurodegenerative disease is Alzheimer’s disease. In embodiments, the neurodegenerative disease is Huntington’s disease. In embodiments, the neurodegenerative disease is Amyotrophic lateral sclerosis. In embodiments, the neurodegenerative disease is Lewy body disease. In embodiments, the neurodegenerative disease is Progressive Supranuclear Palsy. In embodiments, the neurodegenerative disease is Parkinson’s disease. In embodiments, the neurodegenerative disease is frontotemporal degeneration (FTD). In embodiments, the neurodegenerative disease is frontotemporal lobar degeneration (FTLD). In embodiments, the neurodegenerative disease is Pick’s disease.
In an aspect is provided a method of treating a memory loss, the method including administering to a subject in need thereof an effective amount of a compound as disclosed herein.
In an aspect is provided a method of treating axonal degradation, the method including administering to a subject in need thereof an effective amount of a compound as disclosed herein. In embodiments, the method includes treating neuronal loss. In embodiments, the method includes treating brain volume loss.
In an aspect is provided a method of treating an inflammatory disease, the method including administering to a subject in need thereof an effective amount of a compound as disclosed herein. In embodiments, the inflammatory disease is an autoimmune diseases. In embodiments, the inflammatory disease is arthritis. In embodiments, the inflammatory disease is rheumatoid arthritis. In embodiments, the inflammatory disease is psoriatic arthritis. In embodiments. In embodiments, the inflammatory disease is the inflammatory disease is juvenile idiopathic arthritis. In embodiments, the inflammatory disease is multiple sclerosis. In embodiments, the inflammatory disease is systemic lupus erythematosus (SLE). In embodiments, the inflammatory disease is myasthenia gravis. In embodiments, the inflammatory disease is juvenile onset diabetes. In embodiments, the inflammatory disease is diabetes mellitus type 1. In embodiments, the inflammatory disease is Guillain-Barre syndrome. In embodiments, the inflammatory disease is Hashimoto’s encephalitis. In embodiments, the inflammatory disease is Hashimoto’s thyroiditis. In embodiments, the inflammatory disease is ankylosing spondylitis. In embodiments, the inflammatory disease is psoriasis. In embodiments, the inflammatory disease is Sjogren’s syndrome. In embodiments, the inflammatory disease is vasculitis. In embodiments, the inflammatory disease is glomerulonephritis. In embodiments, the inflammatory disease is auto-immune thyroiditis. In embodiments, the inflammatory disease is Behcet’s disease. In embodiments, the inflammatory disease is Crohn’s disease. In embodiments, the inflammatory disease is ulcerative colitis. In embodiments, the inflammatory disease is bullous pemphigoid. In embodiments, the inflammatory disease is sarcoidosis. In embodiments, the inflammatory disease is ichthyosis. In embodiments, the inflammatory disease is Graves ophthalmopathy. In embodiments, the inflammatory disease is inflammatory bowel disease. In embodiments, the inflammatory disease is Addison’s disease. In embodiments, the inflammatory disease is Vitiligo. In embodiments, the inflammatory disease is asthma. In embodiments, the inflammatory disease is allergic asthma. In embodiments, the inflammatory disease is acne vulgaris. In embodiments, the inflammatory disease is celiac disease. In embodiments, the inflammatory disease is chronic prostatitis. In embodiments, the inflammatory disease is inflammatory bowel disease. In embodiments, the inflammatory disease is pelvic inflammatory disease. In embodiments, the inflammatory disease is reperfusion injury. In embodiments, the inflammatory disease is ischemia reperfusion injury. In embodiments, the inflammatory disease is stroke. In embodiments, the inflammatory disease is sarcoidosis. In embodiments, the inflammatory disease is transplant rejection. In embodiments, the inflammatory disease is interstitial cystitis. In embodiments, the inflammatory disease is atherosclerosis. In embodiments, the inflammatory disease is scleroderma. In embodiments, the inflammatory disease is atopic dermatitis.
In an aspect is provided a method of treating neuroinflammation, the method including administering to a subject in need thereof an effective amount of a compound as disclosed herein.
In an aspect is provided a method of treating liver disease, the method including administering to a subject in need thereof an effective amount of a compound as disclosed herein. In embodiments, the liver disease is nonalcoholic steatohepatitis or nonalcoholic fatty liver disease. In embodiments, the liver disease is nonalcoholic steatohepatitis. In embodiments, the liver disease is nonalcoholic fatty liver disease.
In an aspect is provided a method of treating nonalcoholic steatohepatitis or nonalcoholic fatty liver disease, the method including administering to a subject in need thereof an effective amount of a compound as disclosed herein. In embodiments is provided a method of treating nonalcoholic steatohepatitis, the method including administering to a subject in need thereof an effective amount of a compound as disclosed herein. In an aspect is provided a method of treating nonalcoholic fatty liver disease, the method including administering to a subject in need thereof an effective amount of a compound as disclosed herein.
In an aspect is provided a method of treating a fibrotic disease, the method including administering to a subject in need thereof an effective amount of a compound as disclosed herein. In embodiments, the fibrotic disease occurs in the lung, liver, or brain. In embodiments, the fibrotic disease is pulmonary fibrosis. In embodiments, the fibrotic disease is pulmonary fibrosis. In embodiments, the fibrotic disease is cystic fibrosis. In embodiments, the fibrotic disease is idiopathic pulmonary fibrosis. In embodiments, the fibrotic disease is radiation-induced lung injury. In embodiments, the fibrotic disease is bridging fibrosis. In embodiments, the fibrotic disease is cirrhosis. In embodiments, the fibrotic disease is myocardial fibrosis. In embodiments, the fibrotic disease is interstitial fibrosis. In embodiments, the fibrotic disease is replacement fibrosis. In embodiments, the fibrotic disease is glial scar. In embodiments, the fibrotic disease is arterial stiffness. In embodiments, the fibrotic disease is arthrofibrosis. In embodiments, the fibrotic disease is Crohn’s disease. In embodiments, the fibrotic disease is Dupuytren’s contracture. In embodiments, the fibrotic disease is Keloid. In embodiments, the fibrotic disease is Mediastinal fibrosis. In embodiments, the fibrotic disease is Myelofibrosis. In embodiments, the fibrotic disease is Peyronie’s disease. In embodiments, the fibrotic disease is Nephrogenic systemic fibrosis. In embodiments, the fibrotic disease is Progressive massive fibrosis. In embodiments, the fibrotic disease is Retroperitoneal fibrosis. In embodiments, the fibrotic disease is Scleroderma (systemic sclerosis). In embodiments, the fibrotic disease is adhesive capsulitis.
In an aspect is provided a Caspase 6 protein covalently bonded to a compound as described herein. In embodiments, the compound is bonded (e.g., covalently bonded) to a cysteine residue of the protein.
In an aspect is provided a Caspase protein covalently bonded to a portion of a compound as described herein.
Where the compound covalently binds to Caspase 6, a Caspase 6 protein (e.g., human Caspase 6) covalently bonded to a Caspase 6 inhibitor is formed (also referred to herein as a “Caspase 6-compound adduct”), as described below. In embodiments, the resulting covalent bond is reversible. Where the resulting covalent bond is reversible, the bonding reverses upon denaturation of the protein. Thus, in embodiments, the reversibility of a covalent bond between the compound and the Caspase 6 upon denaturation of the Caspase 6 avoids or decreases autoimmune response in a subject subsequent to administration of the compound (relative to irreversibility).
In embodiments, the Caspase 6 protein (e.g., human Caspase 6) is covalently bonded to a Caspase 6 inhibitor (e.g., compound described herein or a portion of a compound described herein). In embodiments, the Caspase 6 protein (e.g., human Caspase 6) is irreversibly covalently bonded to a Caspase 6 inhibitor (e.g., compound described herein or a portion of a compound described herein). In embodiments, the Caspase 6 protein (e.g., human Caspase 6) is reversibly covalently bonded to a Caspase 6 inhibitor (e.g., compound described herein or a portion of a compound described herein). In embodiments, the Caspase 6 protein (e.g., human Caspase 6) is covalently bonded to a portion of a Caspase 6 inhibitor (e.g., compound described herein). In embodiments, the Caspase 6 protein (e.g., human Caspase 6) is irreversibly covalently bonded to a portion of a Caspase 6 inhibitor (e.g., compound described herein). In embodiments, the Caspase 6 protein (e.g., human Caspase 6) is reversibly covalently bonded to a portion of a Caspase 6 inhibitor (e.g., compound described herein). In embodiments, the Caspase 6 inhibitor (e.g., compound described herein) is bonded to a cysteine residue (e.g., Cys264 of human Caspase 6 or cysteine corresponding to Cys264 of human Caspase 6) of the Caspase 6 protein (e.g., human Caspase 6).
In embodiments, the Caspase 6 protein covalently bonded to a Caspase 6 inhibitor or compound described herein is the product of a reaction between the Caspase 6 protein and a Caspase 6 inhibitor or compound described herein. It will be understood that the covalently bonded Caspase 6 protein and Caspase 6 inhibitor (e.g., compound described herein) are the remnants of the reactant Caspase 6 protein and Caspase 6 inhibitor or compound, wherein each reactant now participates in the covalent bond between the Caspase 6 protein and Caspase 6 inhibitor or compound. In embodiments of the covalently bonded Caspase 6 protein and compound described herein, the remnant of the E substituent is a linker including a covalent bond between the Caspase 6 protein and the remainder of the compound described herein. It will be understood by a person of ordinary skill in the art that when a Caspase 6 protein is covalently bonded to a Caspase 6 inhibitor (e.g., compound described herein), the Caspase 6 inhibitor (e.g., compound described herein) forms a remnant of the pre-reacted Caspase 6 inhibitor (e.g., compound described herein) wherein a bond connects the remnant of the Caspase 6 inhibitor (e.g., compound described herein) to the remnant of the Caspase 6 protein (e.g., cysteine sulfur, sulfur of amino acid corresponding to C264 of human Caspase 6, sulfur of C264 of human Caspase 6). The remnant of the Caspase 6 inhibitor (compound described herein) may also be called a portion of the Caspase 6 inhibitor.
It is understood that the examples and embodiments described herein are for illustrative purposes only and that various modifications or changes in light thereof will be suggested to persons skilled in the art and are to be included within the spirit and purview of this application and scope of the appended claims. All publications, patents, and patent applications cited herein are hereby incorporated by reference in their entirety for all purposes.
General information: All evaporations were carried out in vacuo with a rotary evaporator. Analytical samples were dried in vacuo (1-5 mmHg) at rt. Thin layer chromatography (TLC) was performed on silica gel plates, spots were visualized by UV light (214 and 254 nm). Purification by column and flash chromatography was carried out using silica gel (200-300 mesh). Solvent systems are reported as mixtures by volume. All NMR spectra were recorded on a Bruker 400 (400 MHz) spectrometer. 1H chemical shifts are reported in δ values in ppm with the deuterated solvent as the internal standard. Data are reported as follows: chemical shift, multiplicity (s = singlet, d = doublet, t = triplet, q = quartet, br = broad, m = multiplet), coupling constant (Hz), integration. LCMS spectra were obtained on an Agilent 1200 series 6110 or 6120 mass spectrometer with electrospray ionization and excepted as otherwise indicated, the general LCMS condition was as follows: Waters X Bridge C18 column (50 mm × 4.6 mm x 3.5 um), Flow Rate: 2.0 ml/min, the column temperature: 40° C.
The synthesis of (R)-tert-butyl 1-(4-(trifluoromethoxy)phenylcarbamoyl)piperidin-3-ylcarbamate (0026-2).
To a solution of 0026-1 (5.00 g, 25.0 mmol) in DCM (20 mL) was added 1-isocyanato-4-(trifluoromethoxy)benzene (5.08 g, 25.0 mmol) dropwise at room temperature. The mixture was stirred for 2 h. The solid was filtered to give 0026-2 (8.00 g, yield: 79%) as a white solid.
The synthesis of (R)-3-amino-N-(4-(trifluoromethoxy)phenyl)piperidine-1-carboxamide (0026-3).
To a suspension of solution of 0026-2 (4.00 g, 9.93 mmol) in DCM (20.0 mL), was added TFA (6.00 mL) at room temperature. The reaction mixture was stirred for 1 h. The solvent was removed. The residue was partitioned between DCM (50.0 mL) and saturated aq. NaHCO3 (50.0 mL). The organic layer was separated. The aqueous layer was extracted with DCM (2 × 50.0 mL). The combined organic layers were washed with brine (2 × 50.0 mL), dried over anhydrous Na2SO4, filtered and concentrated in vacuo to give 0026-3 (3.00 g, yield: 100.0%) as a yellow solid.
The synthesis of (R)-N-(4-(trifluoromethoxy)phenyl)-3-(vinylsulfonamido)piperidine-1-carboxamide (SU20667-0026-03)
To a solution of 0026-3 (3.66 g, 12.1 mmol) and TEA (3.05 g, 30.2 mmol) in DCM (50.0 mL) was added 2-chloroethanesulfonyl chloride (1.97 g, 12.1 mmol) under ice-water bath. The mixture was allowed to warm to room temperature and stirred for 1 h. Water (50.0 mL) and DCM (100 mL) was added. The organic layer was separated. The aqueous layer was extracted with DCM (2 × 50.0 mL). The combined organic layers were washed with brine (2 × 50.0 mL), dried over anhydrous Na2SO4, filtered and concentrated in vacuo to give crude product which was purified by c.c. (PE/EA=2:1) to give SU20667-0026-03 (2.40 g, yield: 51%) as a white solid. LC-MS (Agilent LCMS 1200-6120, Column: Waters X-Bridge C18 (50 mm*4.6 mm*3.5 µm); Column Temperature: 40° C.; Flow Rate: 2.0 mL/min; Mobile Phase: from 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] to 0% [water + 10 mM NH4HCO3] and 100% [CH3CN] in 1.6 min, then under this condition for 1.4 min, finally changed to 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] in 0.1 min and under this condition for 0.7 min), Purity: 98.43%, Rt =1.933 min; MS Calcd: 393.10; MS Found: 394.2 [M+H]+. HPLC (Agilent HPLC 1200, Column: L-column2 ODS (150 mm*4.6 mm*5.0 µm); Column Temperature: 40° C.; Flow Rate: 1.5 mL/min; Mobile Phase: from 90% [(total 10 mM AcONH4) water/CH3CN=900/100 (v/v)] and 10% [total 10 mM AcONH4) water/CH3CN=100/900 (v/v)] to 15% [total 10 mM AcONH4) water/CH3CN=900/100 (v/v)] and 85% [total 10 mM AcONH4) water/CH3CN=100/900 (v/v)] in 5 min, then under this condition for 10 min, finally changed to 90% [(total 10 mM AcONH4) water/CH3CN=900/100 (v/v)] and 10% [total 10 mM AcONH4) water/CH3CN=100/900 (v/v)] in 0.1 min and under this condition for 5 min), Purity: 100.0%, Rt =9.072 min. 1H NMR (400 MHz, DMSO-d6) δ 8.70 (s, 1 H), 7.50-7.56 (m, 3 H), 7.23 (d, J=8.4 Hz, 2 H), 6.77 (dd, J=16.4 Hz, 10.0 Hz, 1 H), 6.05 (d, J=16.4 Hz, 1 H), 5.95 (d, J=10.0 Hz, 1 H), 4.03-4.07 (m, 1 H), 3.83 (d, J=13.6 Hz, 1 H), 3.04-3.06 (m, 1 H), 2.85-2.90 (m, 1 H), 2.70-2.75 (m, 1 H), 1.87-1.89 (m, 1 H), 1.69-1.71 (m, 1 H), 1.38-1.43 (m, 2 H). Chemical Formula: C15H18F3N3O4S. Molecular Weight: 393.38. Melting point: 47.2-57.8° C. Optical rotation: [a]25D = 17.00 (c = 0.10, CH3OH).
The synthesis of (R)-tert-butyl 1-(4-(1H-pyrazol-1-yl)phenylcarbamoyl)piperidin-3-ylcarbamate (0065-2).
To a solution of 0065-1 (250 mg, 1.57 mmol) and bis(trichloromethyl) carbonate (163 mg, 0.55 mmol) in DCM (5 ml) was added TEA (380 mg, 3.77 mmol) was stirred at rt for 30 min. Added (R)-tert-butyl piperidin-3-ylcarbamate (314 mg, 1.57 mmol). The mixture was stirred at rt for 1 h and purified by C.C. (PE/EA= 4:1) to get 0065-2 (300 mg, 50%) as a yellow solid.
The synthesis of (R)-N-(4-(1H-pyrazol-1-yl)phenyl)-3-aminopiperidine-1-carboxamide (0065-3).
To a solution of 0065-2 (300 mg, 0.78 mmol) in TFA/DCM (5 ml/5 ml) was stirred at room temperature for 2 h, The solvent was removed in vacuo to give 0065-3 (155 mg, 70%) as yellow oil.
The synthesis of (R)-N-(4-(1H-pyrazol-1-yl)phenyl)-3-(vinylsulfonamido)piperidine-1-carboxamide (SU20667-0065-01)
To a solution of 0065-3 (155 mg, 0.54) and TEA (137 mg, 1.35 mmol) in DCM (3 ml) was added dropwise 2-chloroethanesulfonyl chloride (80 mg, 0.49 mmol), the mixture was stirred at room temperature for 1 h and the solvent was removed in vacuo, the resulting residue was purified by prep-HPLC to give SU20667-0065-01 (78.93 mg, 39%) as a white solid. LC-MS (Agilent LCMS 1200-6120, Column: Waters X-Bridge C18 (50 mm*4.6 mm*3.5 µm); Column Temperature: 40° C.; Flow Rate: 2.0 mL/min; Mobile Phase: from 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] to 0% [water + 10 mM NH4HCO3] and 100% [CH3CN] in 1.6 min, then under this condition for 1.4 min, finally changed to 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] in 0.1 min and under this condition for 0.7 min), Purity: 99.52%, Rt =1.674 min; MS Calcd: 375.14; MS Found: 376.3 [M+H]+. HPLC (Agilent HPLC 1200, Column: L-column2 ODS (150 mm*4.6 mm*5.0 µm); Column Temperature: 40° C.; Flow Rate: 1.5 mL/min; Mobile Phase: from 90% [(total 10 mM AcONH4) water/CH3CN=900/100 (v/v)] and 10% [total 10 mM AcONH4) water/CH3CN=100/900 (v/v)] to 15% [total 10 mM AcONH4) water/CH3CN=900/100 (v/v)] and 85% [total 10 mM AcONH4) water/CH3CN=100/900 (v/v)] in 5 min, then under this condition for 10 min, finally changed to 90% [(total 10 mM AcONH4) water/CH3CN=900/100 (v/v)] and 10% [total 10 mM AcONH4) water/CH3CN=100/900 (v/v)] in 0.1 min and under this condition for 5 min), Purity: 99.72%, Rt =7.224 min. 1H NMR (400 MHz, DMSO-d6) δ 8.64 (s, 1 H), 8.38 (d, J=2.4 Hz, 1 H), 7.66-7.69 (m, 3 H), 7.50-7.58 (m, 3 H), 6.78 (dd, J=16.8 Hz, 10.0 Hz, 1 H), 6.49-6.50 (m, 1 H), 6.05 (d, J=16.8 Hz, 1 H), 5.96 (d, J=10.0 Hz, 1 H), 4.05-4.09 (m, 1 H), 3.85 (d, J=12.8 Hz, 1 H), 3.05 (br, 1 H), 2.86-2.88 (m, 1 H), 2.70-2.87 (m, 1 H), 1.89-1.91 (m, 1 H), 1.69-1.70 (m, 1 H), 1.39-1.44 (m, 2 H). Chemical Formula: C17H21N5O3S. Molecular Weight: 375.45. Melting point: 52.7-59.0° C. Optical rotation: [a]25D = 13.00 (c = 0.10, CH3OH).
The synthesis of tert-butyl 1-(4-(trifluoromethoxy)phenylcarbamoyl)-1,2,3,4-tetrahydroquinolin-3-ylcarbamate (0042-2)
To a solution of 0042-1 (620 mg, 2.5 mmol) in DCM (30 mL) was added TEA (757 mg, 7.5 mmol) and 4-(Trifluoromethoxy)phenyl isocyanate (659 mg, 3.25 mmol). The mixture was stirred at rt for 2 h. The mixture was pour into ice water and extracted with DCM (30 mL × 3). The organic layer was dried over Na2SO4, filtered and concentrated. The residue was purified by column chromatography (PE/EA = 4:1) to give 0042-2 (800 mg, 70.9%) as yellow oil.
The synthesis of 3-amino-N-(4-(trifluoromethoxy)phenyl)-3,4-dihydroquinoline-1(2H)-carboxamide (0042-3)
To a solution of 0042-2 (800 mg, 1.77 mmol) in DCM (20 mL) was added TFA (2 mL). It was stirred at rt for 2 h. The mixture was adjusted to pH 9 with Na2CO3 (aq.) and extracted with DCM (20 mL × 3). The organic layer was dried over Na2SO4, filtered and concentrated to give 0042-3 (500 mg, 80.5%) as yellow oil.
The synthesis of N-(4-(trifluoromethoxy)phenyl)-3-(vinylsulfonamido)-3,4-dihydroquinoline-1(2H)-carboxamide (SU20667-0042-01)
To a solution of 0042-3 (150 mg, 0.43 mmol) in DCM (10 mL) was added TEA (123 mg, 1.29 mmol) and 2-chloroethanesulfonyl chloride (84 mg, 0.51 mmol). The mixture was stirred at rt for 2 h. The mixture was pour into ice water and extracted with DCM (20 mL × 3). The organic layer was dried over Na2SO4, filtered and concentrated. The residue was purified by prep-HPLC to give SU20667-0042-01 (67.96 mg, 35.8%) as a white solid. Agilent LCMS 1200-6120, Column: Waters X-Bridge C18 (50 mm*4.6 mm*3.5 µm); Column Temperature: 40° C.; Flow Rate: 2.0 mL/min; Mobile Phase: from 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] to 0% [water + 10 mM NH4HCO3] and 100% [CH3CN] in 1.6 min, then under this condition for 1.4 min, finally changed to 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] in 0.1 min and under this condition for 0.7 min, Purity 100.00%, Rt = 1.882 min; MS Calcd.: 441.1; MS Found: 442.2[M+H]+. Agilent LCMS 1200-6120, Column: Waters X-Bridge C18 (50 mm*4.6 mm*3.5 µm); Column Temperature: 40° C.; Flow Rate: 2.0 mL/min; Mobile Phase: from 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] to 0% [water + 10 mM NH4HCO3] and 100% [CH3CN] in 1.6 min, then under this condition for 1.4 min, finally changed to 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] in 0.1 min and under this condition for 0.7 min, Purity 97.08%, Rt = 9.552 min; MS Calcd.: 441.1; MS Found: 442.2 [M+H]+. 1HNMR (400 MHz, DMSO-d6) δ 9.17 (s, 1 H), 7.64 (br, 1 H), 7.52-7.56 (m, 2 H), 7.27-7.31 (m, 3 H), 7.12-7.18 (m, 2 H), 6.99-7.03 (m, 1 H), 6.81 (dd, J = 16.8 Hz, 10.0 Hz, 1 H), 6.06 (d, J = 16.8 Hz, 1 H), 5.97 (d, J = 9.6 Hz, 1 H), 4.00-4.04 (m, 1 H), 3.50-3.57 (m, 1 H), 3.35-3.41 (m, 1 H), 3.05-3.11 (m, 1 H), 2.66-2.77 (m, 1 H). Melting point: 50.4-52.7° C.
The SU20667-0042-01 (300 mg) was further purified by chiral-HPLC to give SU20667-0042A-01 (75.37 mg, 25.1%) as a white solid and SU20667-0042B-01 (76.18 mg, 25.4%) as a white solid.
SU20667-0042A-01: Agilent LCMS 1200-6120, Column: Waters X-Bridge C18 (50 mm*4.6 mm*3.5 µm); Column Temperature: 40° C.; Flow Rate: 2.0 mL/min; Mobile Phase: from 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] to 0% [water + 10 mM NH4HCO3] and 100% [CH3CN] in 1.6 min, then under this condition for 1.4 min, finally changed to 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] in 0.1 min and under this condition for 0.7 min, Purity 98.47 %, Rt = 2.408 min; MS Calcd.: 441.1; MS Found: 442.2[M+H]+. Agilent LCMS 1200-6120, Column: Waters X-Bridge C18 (50 mm*4.6 mm*3.5 µm); Column Temperature: 40° C.; Flow Rate: 2.0 mL/min; Mobile Phase: from 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] to 0% [water + 10 mM NH4HCO3] and 100% [CH3CN] in 1.6 min, then under this condition for 1.4 min, finally changed to 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] in 0.1 min and under this condition for 0.7 min, Purity 95.24%, Rt = 10.013 min; MS Calcd.: 441.1; MS Found: 442.2 [M+H]+. 1 H NMR (400 MHz, DMSO-d6) δ 9.16 (s, 1 H), 7.67 (s, 1 H), 7.52-7.56 (m, 2 H), 7.27-7.31 (m, 3 H), 7.13-7.18 (m, 2 H), 6.99-7.03 (m, 1 H), 6.81 (dd, J= 16.8 Hz, 10.0 Hz, 1 H), 6.06 (d, J = 16.8 Hz, 1 H), 5.97 (d, J = 10.0 Hz, 1 H), 3.99-4.04 (m, 1 H), 3.49-3.50 (m, 1 H), 3.36-3.41 (m, 1 H), 3.05-3.11 (m, 1 H), 2.66-2.77 (m, 1 H). Melting point: 147.7-148.5° C. Optical rotation: [a]25D = -22.00 (c = 0.10, CH3CN). ee: 100%.
SU20667-0042B-01: Agilent LCMS 1200-6120, Column: Waters X-Bridge C18 (50 mm*4.6 mm*3.5 µm); Column Temperature: 40° C.; Flow Rate: 2.0 mL/min; Mobile Phase: from 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] to 0% [water + 10 mM NH4HCO3] and 100% [CH3CN] in 1.6 min, then under this condition for 1.4 min, finally changed to 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] in 0.1 min and under this condition for 0.7 min, Purity 97.81 %, Rt = 2.430 min; MS Calcd.: 441.1; MS Found: 442.0[M+H]+. Agilent LCMS 1200-6120, Column: Waters X-Bridge C18 (50 mm*4.6 mm*3.5 µm); Column Temperature: 40° C.; Flow Rate: 2.0 mL/min; Mobile Phase: from 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] to 0% [water + 10 mM NH4HCO3] and 100% [CH3CN] in 1.6 min, then under this condition for 1.4 min, finally changed to 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] in 0.1 min and under this condition for 0.7 min, Purity 97.55%, Rt = 10.016 min; MS Calcd.: 441.1; MS Found: 442.0 [M+H]+. 1 H NMR (400 MHz, DMSO-d6) δ 9.16 (s, 1 H), 7.67 (s, 1 H), 7.52-7.56 (m, 2 H), 7.27-7.31 (m, 3 H), 7.12-7.18 (m, 2 H), 6.99-7.03 (m, 1 H), 6.81 (dd, J= 16.4 Hz, 9.6 Hz, 1 H), 6.06 (d, J= 16.4 Hz, 1 H), 5.97 (d, J= 10.0 Hz, 1 H), 3.99-4.04 (m, 1 H), 3.52-3.53 (m, 1 H), 3.36-3.41 (m, 1 H), 3.05-3.11 (m, 1 H), 2.66-2.77 (m, 1 H). Chemical Formula: C19H18F3N3O4S. Molecular Weight: 441.42 Melting point: 146.2-147.9° C. Optical rotation: [a]25D = 14.0 (c = 0.10, CH3CN). ee: 100%.
Scheme 4: Route for SU20667-0067-01
The synthesis of (S)-tert-butyl 4,4-difluoro-1-(4-(trifluoromethoxy)phenylcarbamoyl)piperidin-3-ylcarbamate (0067-2).
To a solution of 0067-1 (118 mg, 0.5 mmol) in DCM (10 mL) was added TEA (151 mg, 1.5 mmol) and 4-(Trifluoromethoxy)phenyl isocyanate (114 mg, 0.56 mmol). The mixture was stirred at rt for 2 h. The mixture was pour into ice water and extracted with DCM (20 mL × 3). The organic layer was dried over Na2SO4, filtered and concentrated. The residue was purified by column chromatography (PE/EA= 4: 1) to give 0067-2 (163 mg, 74.4%) as yellow oil.
The synthesis of (S)-3-amino-4,4-difluoro-N-(4-(trifluoromethoxy)phenyl)piperidine-1-carboxamide (0067-3)
To a solution of 0067-2 (163 mg, 0.37 mmol) in DCM (10 mL) was added TFA (1 mL). It was stirred at rt for 2 h. The mixture was adjusted to pH 9 with Na2CO3 (aq.) and extracted with DCM (20 mL × 3). The organic layer was dried over Na2SO4, filtered and concentrated to give 0067-3 (123 mg, 98.1%) as yellow oil.
The synthesis of (S)-4,4-difluoro-N-(4-(trifluoromethoxy)phenyl)-3-(vinyl-sulfonamido)piperidine-1-carboxamide (SU20667-0067-01)
To a solution of 0067-3 (123 mg, 0.36 mmol) in DCM (10 mL) was added TEA (109 mg, 1.08 mmol) and 2-chloroethanesulfonyl chloride (60 mg, 0.37 mmol). The mixture was stirred at rt. for 2 h. The mixture was pour into ice water and extracted with DCM (10 mL × 3). The organic layer was dried over Na2SO4, filtered and concentrated. The residue was purified by prep-HPLC to give SU20667-0067-01 (106.67 mg, 69.1%) as a white solid. Agilent LCMS 1200-6120, Column: Waters X-Bridge C18 (50 mm*4.6 mm*3 \. 5 µm); Column Temperature: 40° C.; Flow Rate: 2.0 mL/min; Mobile Phase: from 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] to 0% [water + 10 mM NH4HCO3] and 100% [CH3CN] in 1.6 min, then under this condition for 1.4 min, finally changed to 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] in 0.1 min and under this condition for 0.7 min, Purity 97.63 %, Rt = 1.966 min; MS Calcd.: 429.0; MS Found: 430.0[M+H]+. Agilent LCMS 1200-6120, Column: Waters X-Bridge C18 (50 mm*4.6 mm*3.5 µm); Column Temperature: 40° C.; Flow Rate: 2.0 mL/min; Mobile Phase: from 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] to 0% [water + 10 mM NH4HCO3] and 100% [CH3CN] in 1.6 min, then under this condition for 1.4 min, finally changed to 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] in 0.1 min and under this condition for 0.7 min, Purity 98.44%, Rt = 9.282 min; MS Calcd.: 429.0; MS Found: 430.0 [M+H]+. 1 H NMR (400 MHz, DMSO-d6) δ 8.92 (s, 1 H), 7.98 (br, 1 H), 7.54-7.58 (m, 2 H), 7.25 (d, J= 8.4 Hz, 2 H), 6.75 (dd, J = 16.8 Hz, 10.0 Hz, 1 H), 6.06 (d, J = 16.4 Hz, 1 H), 5.96 (d, J = 10.0 Hz, 1 H), 3.92-4.04 (m, 2 H), 3.52-3.60 (m, 1 H), 3.03-3.18 (m, 2 H), 2.01-2.19 (m, 2 H). Chemical Formula: C15H16F5N3O4S. Molecular Weight: 429.36. Melting point: 56.9-69.1° C.
The synthesis of tert-butyl 6-chloro-1,2,3,4-tetrahydroquinolin-3-ylcarbamate (0069-2)
To a solution of 0069-1 (500 mg, 2.02 mmol) in CH3CN (10 ml) was added NBS (360 mg, 2.02 mmol) was stirred at rt for 6 h. Removing the solvent and the resulting residue was purified by CC (PE/EA= 4:1) to get 0069-2 (390 mg, 69%) as a yellow solid.
The synthesis of tert-butyl 6-chloro-1-(4-(trifluoromethoxy)phenylcarbamoyl)-1,2,3,4-tetrahydroquinolin-3-ylcarbamate (0069-3)
To a solution of 0069-2 (390 mg, 1.38) and TEA (348 mg, 3.45 mmol) in DCM (6 ml) was added 4-(Trifluoromethoxy)phenyl isocyanate (280 mg, 1.38 mmol) was stirred at rt for 2 h. Removing the solvent and the resulting residue was purified by CC (PE/EA= 5:1) to get 0069-3 (400 mg, 60%) as yellow oil.
The synthesis of 3-amino-6-chloro-N-(4-(trifluoromethoxy)phenyl)-3,4-dihydroquinoline-1(2H)-carboxamide (0069-4)
To a solution of 0069-3 (400 mg, 0.82 mmol) in TFA/DCM (5 ml/5 ml) was stirred at room temperature for 2 h, The solvent was removed in vacuo to give 0069-4 (390 mg, crude) as colorless oil.
The synthesis of 6-chloro-N-(4-(trifluoromethoxy)phenyl)-3-(vinylsulfonamido)-3,4-dihydroquinoline-1(2H)-carboxamide (SU20667-0069-01).
To a solution of 0069-4 (390 mg, crude) and TEA (323 mg, 3.2 mmol) in DCM (5 ml) was added dropwise 2-chloroethanesulfonyl chloride (209 mg, 1.28 mmol), the mixture was stirred at room temperature for 30 min and the solvent was removed in vacuo and the resulting residue was purified by prep-HPLC to give SU20667-0069-01 (152.87 mg, 25%) as a white solid. LC-MS (Agilent LCMS 1200-6120, Column: Waters X-Bridge C18 (50 mm*4.6 mm*3.5 µm); Column Temperature: 40° C.; Flow Rate: 2.0 mL/min; Mobile Phase: from 90% [(total 10 mM AcONH4) water/CH3CN=900/100 (v/v)] and 10% [(total 10 mM AcONH4) water/CH3CN=100/900 (v/v)] to 10% [(total 10 mM AcONH4) water/CH3CN=900/100 (v/v)] and 90% [(total 10 mM AcONH4) water/CH3CN=100/900 (v/v)] in 1.6 min, then under this condition for 2.4 min, finally changed to 90% [(total 10 mM AcONH4) water/CH3CN=900/100 (v/v)] and 10% [(total 10 mM AcONH4) water/CH3CN=100/900 (v/v)] in 0.1 min and under this condition for 0.7 min), Purity: 97.93%, Rt=2.199 min; MS Calcd: 475.06; MS Found: 476.0 [M+H]+. HPLC (Agilent HPLC 1200, Column: L-column2 ODS (150 mm*4.6 mm*5.0 µm); Column Temperature: 40° C.; Flow Rate: 1.5 mL/min; Mobile Phase: from 90% [(total 10 mM AcONH4) water/CH3CN=900/100 (v/v)] and 10% [total 10 mM AcONH4) water/CH3CN=100/900 (v/v)] to 15% [total 10 mM AcONH4) water/CH3CN=900/100 (v/v)] and 85% [total 10 mM AcONH4) water/CH3CN=100/900 (v/v)] in 5 min, then under this condition for 10 min, finally changed to 90% [(total 10 mM AcONH4) water/CH3CN=900/100 (v/v)] and 10% [total 10 mM AcONH4) water/CH3CN=100/900 (v/v)] in 0.1 min and under this condition for 5 min), Purity:98.44%, Rt =10.532 min. 1H NMR (400 MHz, DMSO-d6) δ 9.20 (s, 1 H), 7.67 (s, 1 H), 7.52-7.55 (m, 2 H), 7.26-7.35 (m, 4 H), 7.17-7.20 (m, 1 H), 6.80 (dd, J=16.8 Hz, 10.0 Hz, 1 H), 6.06 (d, J=16.8 Hz, 1 H), 5.97 (d, J=10.0 Hz, 1 H), 3.96-4.00 (m, 1 H), 3.54-3.55 (m, 1 H), 3.40-3.45 (m, 1 H), 3.05-3.11 (m, 1 H), 2.70-2.75 (m, 1 H). Chemical Formula: C19H17ClF3N3O4S. Molecular Weight: 475.87. Melting point: 156.5-157.4° C.
The synthesis of (R)-tert-butyl 1-(3-fluoro-4-(trifluoromethoxy)phenylcarbamoyl)piperidin-3-ylcarbamate (0076-2).
To a solution of 0076-1 (100 mg, 0.51 mmol) and bis(trichloromethyl) carbonate (53 mg, 0.35 mmol) in DCM (3 ml) was added TEA (122 mg, 1.12 mmol) was stirred at rt for 30 min. Added (R)-tert-butyl piperidin-3-ylcarbamate (103 mg, 0.51 mmol). The mixture was stirred at rt for 2 h and purified by CC to get 0076-2 (350 mg, crude) as a white solid.
The synthesis of (R)-3-amino-N-(3-fluoro-4-(trifluoromethoxy)phenyl)piperidine-1-carboxamide (0076-3)
To a solution of 0076-2 (350 mg, crude) in TFA/DCM (5 ml/5 ml) was stirred at room temperature for 2 h, The solvent was removed in vacuo to give 0076-3 (160 mg, 60%) as yellow oil.
The synthesis of (R)-N-(3-fluoro-4-(trifluoromethoxy)phenyl)-3-(vinylsulfonamido)piperidine-1-carboxamide (SU20667-0076-01)
To a solution of 0076-3 (160 mg, 0.5 mmol) and TEA (126 mg, 1.25 mmol) in DCM (3 ml) was added dropwise 2-chloroethanesulfonyl chloride (82 mg, 0.5 mmol), the mixture was stirred at room temperature for 1 h and the solvent was removed in vacuo and the resulting residue was purified by prep-HPLC to get SU20667-0076-01 (34.39 mg, 17%) as a white solid. LC-MS (Agilent LCMS 1200-6120, Column: Waters X-Bridge C18 (50 mm*4.6 mm*3.5 µm); Column Temperature: 40° C.; Flow Rate: 2.0 mL/min; Mobile Phase: from 90% [(total 10 mM AcONH4) water/CH3CN=900/100 (v/v)] and 10% [(total 10 mM AcONH4) water/CH3CN=100/900 (v/v)] to 10% [(total 10 mM AcONH4) water/CH3CN=900/100 (v/v)] and 90% [(total 10 mM AcONH4) water/CH3CN=100/900 (v/v)] in 1.6 min, then under this condition for 2.4 min, finally changed to 90% [(total 10 mM AcONH4) water/CH3CN=900/100 (v/v)] and 10% [(total 10 mM AcONH4) water/CH3CN=100/900 (v/v)] in 0.1 min and under this condition for 0.7 min), Purity: 99.14%, Rt=1.977 min; MS Calcd: 411.09; MS Found: 412.2 [M+H]+. HPLC (Agilent HPLC 1200, Column: L-column2 ODS (150 mm*4.6 mm*5.0 µm); Column Temperature: 40° C.; Flow Rate: 1.5 mL/min; Mobile Phase: from 90% [(total 10 mM AcONH4) water/CH3CN=900/100 (v/v)] and 10% [total 10 mM AcONH4) water/CH3CN=100/900 (v/v)] to 15% [total 10 mM AcONH4) water/CH3CN=900/100 (v/v)] and 85% [total 10 mM AcONH4) water/CH3CN=100/900 (v/v)] in 5 min, then under this condition for 10 min, finally changed to 90% [(total 10 mM AcONH4) water/CH3CN=900/100 (v/v)] and 10% [total 10 mM AcONH4) water/CH3CN=100/900 (v/v)] in 0.1 min and under this condition for 5 min), Purity:99.18%, Rt =9.313 min. 1H NMR (400 MHz, DMSO-d6) δ 8.89 (s, 1 H), 7.66 (dd, J=13.6 Hz, 2.8 Hz, 1 H), 7.50-7.52 (m, 1 H), 7.39-7.43 (m, 1 H), 7.30-7.32 (m, 1 H), 6.77 (dd, J=16.8 Hz, 10.0 Hz, 1 H), 6.04 (d, J=16.4 Hz, 1 H), 5.95 (d, J=10.0 Hz, 1 H), 4.03 (dd, J=12,4 Hz, 4.0 Hz, 1 H), 3.81 (d, J=12.8 Hz, 1 H), 3.04-3.05 (m, 1 H), 2.70-2.90 (m, 1 H), 2.73-2.90 (m, 1 H), 1.88-1.89 (m, 1 H), 1.60-1.70 (m, 1 H), 1.42 (t, J=9.2 Hz, 2 H). Chemical Formula: C15H17F4N3O4S. Molecular Weight: 411.37. Melting point: 41.1-49.2° C. Optical rotation: [a]25D = 5.00 (c = 0.10, CH3CN)
The synthesis of 2-chloro-N-(4-(trifluoromethoxy)phenyl)acetamide (0088-2)
To a mixture of 0088-1 (200 mg, 1.13 mmol) in DCM (10 mL) was added 2-chloroacetyl chloride (152 mg, 1.36 mmol). It was stirred at rt for 2 h. The reaction mixture was concentrated to give 0088-2 (220 mg crude) as yellow oil.
The synthesis of (R)-tert-butyl 1-(2-oxo-2-(4-(trifluoromethoxy)phenylamino)ethyl)piperidin-3-ylcarbamate (0088-3)
To a solution of 0088-2 (220 mg, 0.87 mmol) in DMF (5 mL) was added (R)-tert-butyl piperidin-3-ylcarbamate (226 mg, 1.13 mmol) and Cs2CO3 (850 mg, 2.61 mmol). It was stirred at rt overnight. Water (40 mL) was added and extracted with EA (20 mL × 3). The organic layer was dried over Na2SO4, filtered and concentrated. The residue was purified by column chromatography (PE/EA= 4:1) to give 0088-3 (333 mg, 91.9%) as a white solid.
The synthesis of (R)-2-(3-aminopiperidin-1-yl)-N-(4-(trifluoromethoxy)phenyl)acetamide (0088-4)
To a solution of 0088-3 (333 mg, 0.8 mmol) in DCM (10 mL) was added TFA (1 mL). It was stirred at rt for 2 h. The mixture was adjusted to pH 9 with Na2CO3 (aq.) and extracted with DCM (20 mL × 3). The organic layer was dried over Na2SO4, filtered and concentrated to give 0088-4 (150 mg, 59.1%) as yellow oil.
The synthesis of (R)-N-(4-(trifluoromethoxy)phenyl)-2-(3-(vinylsulfonamido)piperidin-1-yl)acetamide (SU20667-0088-01)
To a solution of 0088-4 (150 mg, 0.47 mmol) in DCM (10 mL) was added TEA (142 mg, 1.41 mmol) and 2-chloroethanesulfonyl chloride (99 mg, 0.61 mmol). The mixture was stirred at rt for 2 h. The mixture was pour into ice water and extracted with DCM (20 mL × 3). The organic layer was dried over Na2SO4, filtered and concentrated. The residue was purified by prep-HPLC to give SU20667-0088-01 (48.22 mg, 25.2%) as a white solid. Agilent LCMS 1200-6120, Column: Waters X-Bridge C18 (50 mm*4.6 mm*3.5 µm); Column Temperature: 40° C.; Flow Rate: 2.0 mL/min; Mobile Phase: from 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] to 0% [water + 10 mM NH4HCO3] and 100% [CH3CN] in 1.6 min, then under this condition for 1.4 min, finally changed to 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] in 0.1 min and under this condition for 0.7 min, Purity 98.51 %, Rt = 2.034 min; MS Calcd.: 407.1; MS Found: 407.8 [M+H]+. Agilent LCMS 1200-6120, Column: Waters X-Bridge C18 (50 mm*4.6 mm*3.5 µm); Column Temperature: 40° C.; Flow Rate: 2.0 mL/min; Mobile Phase: from 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] to 0% [water + 10 mM NH4HCO3] and 100% [CH3CN] in 1.6 min, then under this condition for 1.4 min, finally changed to 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] in 0.1 min and under this condition for 0.7 min, Purity 97.62%, Rt = 9.509 min; MS Calcd.: 407.1; MS Found: 408.2 [M+H]+. 1 H NMR (400 MHz, DMSO-d6) δ 9.86 (s, 1 H), 7.72-7.76 (m, 2 H), 7.50 (d, J = 4.4 Hz, 1 H), 7.33 (d, J = 8.4 Hz, 2 H), 6.03 (dd, J = 16.4 Hz, 9.6 Hz, 1 H), 6.02 (d, J= 16.4 Hz, 1 H), 5.87 (d, J= 10.0 Hz, 1 H), 3.06-3.33 (m, 4 H), 2.72-2.75 (m, 1 H), 2.19-2.26 (m, 2 H), 1.68-1.71 (m, 2 H), 1.50-1.53 (m, 1 H), 1.28-1.30 (m, 1 H). Chemical Formula: C16H20F3N3O4S. Molecular Weight: 407.41. Melting point: 112.8-113.5° C. Optical rotation: [a]25D = 19.50 (c = 0.20, CH3OH).
The synthesis of ethyl 2-(4-(trifluoromethoxy)phenylamino)acetate (0089-2)
To a solution of 0089-1 (500 mg, 2.82 mmol) in DMF (30 mL) was added K2CO3 (1.17 g, 8.46 mmol) and ethyl 2-bromoacetate (562 mg, 3.38 mmol) and stirred at 60° C. for 2 h. The mixture was pour into ice water and extracted with DCM (30 mL × 3). The organic layer was dried over Na2SO4, filtered and concentrated. The residue was purified by column chromatography (PE/EA= 3: 1) to give 0089-2 (550 mg, 74.1%) as a white solid.
The synthesis of ethyl 2-(4-(trifluoromethoxy)phenylamino)acetic acid (0089-3)
To a solution of 0089-2 (550 mg, 1.6 mmol) in CH3OH (20 mL) was added 1 N LiOH (20 mL). It was stirred at rt for 2 h. The mixture was adjusted to pH 5 with 2 N HCl (in water) and extracted with DCM (20 mL × 3). The organic layer was dried over Na2SO4, filtered and concentrated to give 0089-3 (250 mg, 66.2%) as yellow oil.
The synthesis of ethyl (R)-tert-butyl 1-(2-(4-(trifluoromethoxy)phenylamino)acetyl)piperidin-3-ylcarbamate (0089-4)
To a solution of 0089-3 (249 mg, 1.06 mmol) in DMF (10 mL) was EDCI (265 mg, 1.38 mmol), DMAP (194 mg, 1.59 mmol) and (R)-tert-butyl piperidin-3-ylcarbamate (276 mg, 1.38 mmol) and stirred at rt overnight. The mixture was pour into ice water and extracted with DCM (30 mL × 3). The organic layer was dried over Na2SO4, filtered and concentrated. The residue was purified by column chromatography (PE:EA= 2:1) to give 0089-4 (300 mg, 67.8%) as a white solid.
The synthesis of (R)-1-(3-aminopiperidin-1-yl)-2-(4-(trifluoromethoxy)phenyl-amino)ethanone (0089-5)
To a solution of 0089-4 (300 mg, 0.72 mmol) in DCM (10 mL) was added TFA (1 mL). It was stirred at rt for 2 h. The mixture was adjusted to pH 9 with Na2CO3 (aq.) and extracted with DCM (20 mL × 3). The organic layer was dried over Na2SO4, filtered and concentrated to give 0089-5 (200 mg, 87.6%) as yellow oil.
The synthesis of (R)-N-(1-(2-(4-(trifluoromethoxy)phenylamino)acetyl)piperidin-3-yl)ethenesulfonamide (SU20667-0089-01)
To a solution of 0089-5 (200 mg, 0.63 mmol) in DCM (10 mL) was added TEA (191 mg, 1.89 mmol) and 2-chloroethanesulfonyl chloride (133 mg, 0.82 mmol). The mixture was stirred at rt for 2 h. The mixture was pour into ice water and extracted with DCM (20 mL × 3). The organic layer was dried over Na2SO4, filtered and concentrated. The residue was purified by prep-HPLC to give SU20667-0089-01 (32.19 mg, 12.6%) as a white solid. Agilent LCMS 1200-6120, Column: Waters X-Bridge C18 (50 mm*4.6 mm*3.5 µm); Column Temperature: 40° C.; Flow Rate: 2.0 mL/min; Mobile Phase: from 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] to 0% [water + 10 mM NH4HCO3] and 100% [CH3CN] in 1.6 min, then under this condition for 1.4 min, finally changed to 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] in 0.1 min and under this condition for 0.7 min, Purity 97.95 %, Rt = 2.001 min; MS Calcd.: 407.1; MS Found: 408.1 [M+H]+. Agilent LCMS 1200-6120, Column: Waters X-Bridge C18 (50 mm*4.6 mm*3.5 µm); Column Temperature: 40° C.; Flow Rate: 2.0 mL/min; Mobile Phase: from 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] to 0% [water + 10 mM NH4HCO3] and 100% [CH3CN] in 1.6 min, then under this condition for 1.4 min, finally changed to 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] in 0.1 min and under this condition for 0.7 min, Purity 95.41%, Rt = 9.329 min; MS Calcd.: 407.1; MS Found: 408.2 [M+H]+. 1HNMR (400 MHz, DMSO-d6) δ 7.52-7.58 (m, 1 H), 7.04-7.06 (m, 2 H), 6.64-6.68 (m, 3 H), 5.84-6.09 (m, 3 H), 3.94-4.17 (m, 1 H), 3.62-3.88 (m, 3 H), 2.73-3.20 (m, 3 H), 1.32-1.87 (m, 4 H). Chemical Formula: C16H20F3N3O4S. Molecular Weight: 407.41. Melting point: 151.6-153.9° C. Optical rotation: [a]25D = 15.00 (c = 0.20, CH3OH)
The synthesis of N-(2-chloroethyl)-4-(trifluoromethoxy)aniline (104-2)
To a mixture of 104-1 (1 g, 5.65 mmol) in CH3OH (20 mL) was added 2-chloroacetaldehyde (529 mg, 6.78 mmol) and AcOH (407 mg, 6.78 mmol). It was stirred at rt for 1 h. Then NaCNBH3 (712 mg, 11.3 mmol) was added and stirred at rt for 1 h. Water (20 mL) was added and extracted with EA (20 mL × 3). The organic layer was dried over Na2SO4, filtered and concentrated. The residue was purified by column chromatography (PE/EA= 2:1) to give 104-2 (1.1 g, 81.4%) as yellow oil.
The synthesis of (R)-benzyl 1-(2-(4-(trifluoromethoxy)phenylamino)ethyl)piperidin-3-ylcarbamate (104-3)
To a solution of 104-2 (1.1 g, 4.6 mmol) in CH3CN (50 mL) was added (R)-tert-butyl piperidin-3-ylcarbamate (1.4 g, 5.98 mmol), KI (992 mg, 5.98 mmol) and Cs2CO3 (4.5 g, 13.8 mmol). It was subjected to MW condition at 100° C. for 1 h. Water (40 mL) was added and extracted with EA (20 mL × 3). The organic layer was dried over Na2SO4, filtered and concentrated. The residue was purified by column chromatography (PE/EA= 1: 1) to give 104-3 (1 g, 49.7%) as yellow oil.
The synthesis of 104-4
To a solution of 104-3 (1 g, 2.3 mmol) in DCM (30 mL) was added (Boc)2O (602 mg, 2.76 mmol), DMAP (28 mg, 0.23 mmol) and Et3 N (697 mg, 6.9 mmol). It was stirred at 50° C. overnight. Water (40 mL) was added and extracted with DCM (20 mL × 3). The organic layer was dried over Na2SO4, filtered and concentrated. The residue was purified by column chromatography (PE/EA=4:1) to give 104-4 (500 mg, 40.4%) as yellow oil.
The synthesis of (R)-tert-butyl 2-(3-aminopiperidin-1-yl)ethyl(4-(trifluoromethoxy)phenyl)carbamate (104-5)
To a solution of 104-4 (500 mg, 0.93 mmol) in CH3OH (10 mL) was added Pd/C (50 mg). The mixture was stirred at rt overnight under H2 (1.0 atm) overnight. The mixture was filtered through a Celite pad, and the filtrate was concentrated to give 104-5 (300 mg crude) as yellow oil.
The synthesis of (R)-tert-butyl 4-(trifluoromethoxy)phenyl(2-(3-(vinylsulfonamido)piperidin-1-yl)ethyl)carbamate (104-6)
To a solution of 104-5 (300 mg, 0.74 mmol) in DCM (20 mL) was added TEA (97 mg, 0.96 mmol) and 2-chloroethanesulfonyl chloride (133 mg, 0.81 mmol). The mixture was stirred at rt for 1 h. The mixture was pour into ice water and extracted with DCM (20 mL × 3). The organic layer was dried over Na2SO4, filtered and concentrated give 104-6 (250 mg, 68.5%) as yellow oil.
The synthesis of (R)-N-(1-(2-(4-(trifluoromethoxy)phenylamino)ethyl)piperidin-3-yl)ethenesulfonamide (SU20667-0104-01)
To a solution of 104-6 (250 mg, 0.5 mmol) in dixoxane (10 mL) was added 4 N HCl (10 mL, in dixoxane). It was stirred at rt for 2 h. The mixture concentrated and purified by prep-HPLC to give SU20667-0104-01 (11.01 mg, 5.6%) as a white solid. Agilent LCMS 1200-6120, Column: Waters X-Bridge C18 (50 mm*4.6 mm*3.5 µm); Column Temperature: 40° C.; Flow Rate: 2.0 mL/min; Mobile Phase: from 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] to 0% [water + 10 mM NH4HCO3] and 100% [CH3CN] in 1.6 min, then under this condition for 1.4 min, finally changed to 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] in 0.1 min and under this condition for 0.7 min, Purity 97.52 %, Rt = 2.151 min; MS Calcd.: 393.1; MS Found: 394.1[M+H]+. Agilent HPLC 1200, Column: Waters X-Bridge C18 (150 mm*4.6 mm*3.5 µm); Column Temperature: 40° C.; Flow Rate: 1.0 mL/min; Mobile Phase: from 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] to 0% [water + 10 mM NH4HCO3] and 100% [CH3CN] in 10 min, then under this condition for 5 min, finally changed to 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] in 0.1 min and under this condition for 5 min, Purity 99.19%, Rt = 10.185 min; MS Calcd.: 393.1; MS Found: 394.3 [M+H]+. 1HNMR (400 MHz, CD3OD) δ 7.02 (d, J= 8.4 Hz, 2 H), 6.62-6.68 (m, 3 H), 6.13 (t, J= 16.8 Hz, 1 H), 5.87 (d, J= 10.0 Hz, 1 H), 3.15-3.33 (m, 3 H), 2.86-2.91 (m, 1 H), 2.58-2.70 (m, 3 H), 2.11-2.20 (m, 2 H), 1.74-1.88 (m, 2 H), 1.55-1.64 (m, 1 H), 1.33-1.40 (m, 1 H). Chemical Formula: C16H22F3N3O3S. Molecular Weight: 393.42
The synthesis of 2-(chloromethyl)-5-(trifluoromethoxy)-1H-benzo[d]imidazole (125-2)
A mixture of 125-1 (1 g, 5.2 mmol) and 2-chloroacetic acid (1 g, 10.4 mmol) in 37% aq.HCl solution (20 ml), the resulting mixture was stirred for 5 h at 100° C. The mixture solution was cooled to room temperature and acidified to pH = 6~8 with 2 N aq.NaHCO3 and extracted with EA (15 ml × 3). The organic layer dried over Na2SO4, and evaporated to get 125-2 (700 mg, 54 %) as a yellow solid.
The synthesis of (R)-N-(1-((5-(trifluoromethoxy)-1H-benzo[d]imidazol-2-yl)methyl)piperidin-3-yl)ethenesulfonamide (SU20667-125-01)
The solution of 125-2 (180 mg, 0.72 mmol), (R)-N-(piperidin-3-yl)ethenesulfonamide (137 mg, 0.72 mmol), in DMF (2 ml) was added TEA (218 mg, 2.16 mmol), the mixture was stirred at room temperature for 2 h, then filtered and the solution was purified prep-HPLC to give SU20667-0125-01 (33.08 mg, 11%) as a white solid. LC-MS (Agilent LCMS 1200-6120, Column: Waters X-Bridge C18 (50 mm*4.6 mm*3.5 µm); Column Temperature: 40° C.; Flow Rate: 2.0 mL/min; Mobile Phase: from 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] to 0% [water + 10 mM NH4HCO3] and 100% [CH3CN] in 1.6 min, then under this condition for 1.4 min, finally changed to 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] in 0.1 min and under this condition for 0.7 min), Purity: 99.09%, Rt =1.945 min; MS Calcd.: 404.41; MS Found: 405.2 [M+H]+. HPLC (Agilent HPLC 1200, Column: L-column2 ODS (150 mm*4.6 mm*5.0 µm); Column Temperature: 40° C.; Flow Rate: 1.5 mL/min; Mobile Phase: from 90% [(total 10 mM AcONH4) water/CH3CN=900/100 (v/v)] and 10% [total 10 mM AcONH4) water/CH3CN=100/900 (v/v)] to 15% [total 10 mM AcONH4) water/CH3CN=900/100 (v/v)] and 85% [total 10 mM AcONH4) water/CH3CN=100/900 (v/v)] in 5 min, then under this condition for 10 min, finally changed to 90% [(total 10mM AcONH4) water/CH3CN=900/100 (v/v)] and 10% [total 10 mM AcONH4) water/CH3CN=100/900 (v/v)] in 0.1 min and under this condition for 5 min), Purity:98.01%, Rt =8.973 min. 1H NMR (400 MHz, DMSO-d6) δ 12.54 (s, 1 H), 7.50-7.57 (m, 2 H), 7.36 (s, 1 H), 7.14 (d, J=8.4 Hz, 1 H), 6.70 (dd, J=16.8 Hz, 10.0 Hz, 1 H), 5.99 (d, J=16.4 Hz, 1 H), 5.83 (d, J=10.0 Hz, 1 H), 3.69-3.78 (m, 2 H), 3.19 (s, 1 H), 2.82 (d, J=9.2 Hz, 1 H), 2.54-2.58 (m, 1 H), 2.06 (t, J=8.8 Hz, 2 H), 1.71-1.74 (m, 1 H), 1.62-1.66 (m, 1 H), 1.41-1.49 (m, 1 H), 1.21-1.26 (m, 1 H). Chemical Formula: C16H19F3N4O3S. Molecular Weight: 404.41. Melting point: 65.5-78.4° C. Optical rotation: [a]25D = 30.00 (c = 0.20, CH3OH)
The synthesis of 2-fluoro-4-nitrobenzoic acid (130-2)
A mixture of 134-1 (5 g, 25.6 mmol) in Ac2O (30 mL) was stirred at 40° C. overnight. The reaction mixture was concentrated to give 134-2 (4 g, 66%) as yellow oil.
The synthesis of N-(5-fluoro-2-nitro-4-(trifluoromethoxy)phenyl)acetamide (134-3)
To a solution of 134-2 (4 g, 16.8 mmol) in Ac2O (10 mL) was added HNO3 (1.6 mL, 16.8 mmol) and H2O (10 mL). It was stirred at 40° C. for 1 hour. Water (20 mL) was added and extracted with EA (10 mL × 3). The organic layer was dried over Na2SO4, filtered and concentrated. The residue was purified by column chromatography (PE/EA=1:1) to give 134-3 (2.3 g, 48.5%) as yellow oil.
The synthesis of 5-fluoro-2-nitro-4-(trifluoromethoxy)aniline (134-4)
To a solution of 134-3 (1 g, 3.5 mmol) in 1, 4-dioxane (10 mL) was added 2 N HCl (in water) (10 mL). It was stirred at 100° C. overnight. The mixture was adjusted to pH 9 with Na2CO3 (aq.) and extracted with EA (10 mL × 3). The organic layer was dried over Na2SO4, filtered and concentrated to give 134-4 (700 mg, 83.3%) as yellow oil.
The synthesis of 4-fluoro-5-(trifluoromethoxy)benzene-1,2-diamine (134-5)
To a solution of 134-4 (700 mg, 2.9 mmol) in CH3OH (10 mL) was added Zn (565 mg, 8.7 mmol) and NH4Cl (922 mg, 17.4 mmol). The mixture was stirred at rt for 2 h. The mixture was filtered through a Celite pad, and the filtrate was concentrated to give 134-5 (430 mg, 70.6%) as brown oil.
The synthesis of 2-(chloromethyl)-6-fluoro-5-(trifluoromethoxy)-1H-benzo[d]imidazole (134-6)
To a solution of 134-5 (430 mg, 2 mmol) in HCl (10.0 N, 10 mL) was added 2-chloroacetic acid (207 mg, 2.2 mmol). It was stirred at 100° C. for 5 h. The mixture was adjusted to pH 9 with Na2CO3 (aq.) and extracted with EA (10 mL × 3). The organic layer was dried over Na2SO4, filtered and concentrated to give 134-6 (300 mg, 56%) as yellow oil.
The synthesis of (R)-N-(1-((6-fluoro-5-(trifluoromethoxy)-1H-benzo[d]imidazol-2-yl) methyl) piperidin-3-yl) ethenesulfonamide (SU20667-0134-01)
To a solution of 134-6 (300 mg, 1.1 mmol) in DMF (5 mL) was added (R)-N-(piperidin-3-yl)ethenesulfonamide (373 mg, 1.65 mmol) and Cs2CO3 (1.1 g, 3.3 mmol). It was stirred at rt overnight. Water (40 mL) was added and extracted with EA (20 mL × 3). The organic layer was dried over Na2SO4, filtered and concentrated. The residue was purified by prep-HPLC to give SU20667-0134-01 (67.99 mg, 14.6%) as a white solid. Agilent LCMS 1200-6120, Column: Waters X-Bridge C18 (50 mm*4.6 mm*3.5 µm); Column Temperature: 40° C.; Flow Rate: 2.0 mL/min; Mobile Phase: from 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] to 0% [water + 10 mM NH4HCO3] and 100% [CH3CN] in 1.6 min, then under this condition for 1.4 min, finally changed to 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] in 0.1 min and under this condition for 0.7 min, Purity 100.00 %, Rt = 1.956 min; MS Calcd.: 422.1; MS Found: 423.2 [M+H]+. Agilent HPLC 1200, Column: Waters X-Bridge C18 (150 mm*4.6 mm*3.5 µm); Column Temperature: 40° C.; Flow Rate: 1.0 mL/min; Mobile Phase: from 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] to 0% [water + 10 mM NH4HCO3] and 100% [CH3CN] in 10 min, then under this condition for 5 min, finally changed to 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] in 0.1 min and under this condition for 5 min, Purity 99.46 %, Rt = 8.701 min; MS Calcd.: 422.1; MS Found: 423.2 [M+H]+. 1 H NMR (400 MHz, DMSO-d6) δ 12.67 (s, 1 H), 7.74-7.53 (m, 2 H), 7.38 (d, J = 7.6 Hz, 1 H), 6.71 (dd, J = 16.4 Hz, 10.0 Hz, 1 H), 5.99 (d, J = 16.4 Hz, 1 H), 5.84 (d, J = 9.6 Hz, 1 H), 3.69-3.77 (m, 2 H), 3.17-3.19 (m, 1 H), 2.82-2.84 (m, 1 H), 2.49-2.82 (m, 1 H), 2.03-2.08 (m, 2 H), 1.62-1.75 (m, 2 H), 1.40-1.49 (m, 1 H), 1.18-1.26 (m, 1 H). Chemical Formula: C16H18F4N4O3S. Molecular Weight: 422.40. Melting point: 51.8-57.5° C. Optical rotation: [a]20D = 29.50 (c = 0.20, CH3OH).
The synthesis of 2-iodo-4-(trifluoromethoxy)aniline (135-2)
To a solution of 135-1 (3 g, 16.9 mmol) in EtOH (40 mL) was added Ag2SO4 (312 mg, 16.9 mmol) and I2 (4.29 g, 16.9 mmol). The mixture was stirred at rt for 1 h. The mixture was filtered through a Celite pad, and the filtrate was concentrated. The residue was purified by column chromatography (PE/EA= 2:1) to give 135-2 (4 g, 73.3%) as yellow oil.
The synthesis of 5-(trifluoromethoxy)-1H-indole-2-carboxylic acid (135-3)
To a solution of 135-2 (4 g, 13.2 mmol) in DMF (20 mL) was added 2-oxopropanoic acid (3.48 g, 39.6 mmol), DABCO (4.43 g, 39.6 mmol) and Pd(OAc)2 (296 mg, 1.32 mmol). It was stirred under N2 at 105° C. for 4 h. Water (60 mL) was added and extracted with EA (40 mL × 3). The organic layer was dried over Na2SO4, filtered and concentrated. The residue was purified by column chromatography (DCM/MeOH= 15:1) to give 135-3 (2 g, 61.8%) as yellow oil.
The synthesis of (R)-tert-butyl 1-(5-(trifluoromethoxy)-1H-indole-2-carbonyl)piperidin-3-ylcarbamate (135-4)
To a solution of 135-3 (0.6 g, 1.4 mmol) in DCM (20 mL) was added EDCI (349 mg, 1.82 mmol), DMAP (342 mg, 2.8 mmol) and (R)-tert-butyl piperidin-3-ylcarbamate (364 mg, 1.82 mmol). It was stirred at rt for 16 h. The mixture was washed with 1 N Citric acid (in water) (20 mL × 3). The organic layer was dried over Na2SO4, filtered and concentrated to give 135-4 (700 mg, crude) as yellow oil.
The synthesis of (R)-tert-butyl 1-((5-(trifluoromethoxy)-1H-indol-2-yl)methyl)piperidin-3-ylcarbamate (135-5)
To a solution of 135-4 (700 mg, 1.6 mmol) in THF (20 mL) was added BH3/THF (1.0 N, 16 mL, 16 mmol). The mixture was stirred at rt for 2 d. The mixture was pour into ice water and extracted with DCM (20 mL × 3). The organic layer was dried over Na2SO4, filtered and concentrated. The residue was purified by column chromatography (DCM/MeOH= 20:1) to give 135-5 (450 mg, 68.1%) as yellow oil.
The synthesis of (R)-1-((5-(trifluoromethoxy)-1H-indol-2-yl)methyl)piperidin-3-amine (135-6)
To a solution of 135-5 (450 mg, 1.09 mmol) in DCM (20 mL) was added TFA (2 mL). It was stirred at rt for 2 h. The mixture was adjusted to pH 9 with Na2CO3 (aq.) and extracted with DCM (20 mL × 3). The organic layer was dried over Na2SO4, filtered and concentrated to give 135-6 (300 mg, 88.7%) as yellow oil.
The synthesis of (R)-N-(1-((5-(trifluoromethoxy)-1H-indol-2-yl)methyl)piperidin-3-yl)ethenesulfonamide (SU20667-0135-01)
To a solution of 135-6 (300 mg, 0.96 mmol) in DCM (20 mL) was added TEA (194 mg, 1.92 mmol) and 2-chloroethanesulfonyl chloride (171 mg, 1.05 mmol). The mixture was stirred at rt for 2 h. The mixture was pour into ice water and extracted with DCM (20 mL × 3). The organic layer was dried over Na2SO4, filtered and concentrated. The residue was purified by prep-HPLC to give SU20667-0135-01 (11.19 mg, 2.9%) as a white solid. Agilent LCMS 1200-6120, Column: Waters X-Bridge C18 (50 mm*4.6 mm*3.5 µm); Column Temperature: 40° C.; Flow Rate: 2.0 mL/min; Mobile Phase: from 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] to 0% [water + 10 mM NH4HCO3] and 100% [CH3CN] in 1.6 min, then under this condition for 1.4 min, finally changed to 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] in 0.1 min and under this condition for 0.7 min, Purity 98.43%, Rt = 2.174 min; MS Calcd.: 403.1; MS Found: 404.3[M+H]+. Agilent HPLC 1200, Column: Waters X-Bridge C18 (150 mm*4.6 mm*3.5 µm); Column Temperature: 40° C.; Flow Rate: 1.0 mL/min; Mobile Phase: from 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] to 0% [water + 10 mM NH4HCO3] and 100% [CH3CN] in 10 min, then under this condition for 5 min, finally changed to 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] in 0.1 min and under this condition for 5 min, Purity 96.96 %, Rt = 9.885 min; MS Calcd.: 403.1; MS Found: 404.3 [M+H]+. 1H NMR (400 MHz, DMSO-d6) δ 11.28 (s, 1 H), 7.42 (s, 1 H), 7.38 (d, J = 8.8 Hz, 1 H), 6.99 (dd, J = 8.8 Hz, 1.2 Hz, 1 H), 6.69 (dd, J= 16.4 Hz, 10.0 Hz, 1 H), 6.33 (s, 1 H), 5.98 (d, J= 16.8 Hz, 1 H), 5.82 (d, J= 10.0 Hz, 1 H), 3.57-3.66 (m, 2 H), 3.12-3.17 (m, 1 H), 2.81-2.83 (m, 1 H), 2.50-2.58 (m, 1 H), 1.60-1.94 (m, 4 H), 1.40-1.43 (m, 1 H), 1.18-1.21 (m, 1 H). Chemical Formula: C17H20F3N3O3S. Molecular Weight: 403.42. Melting point: 36.8-40.2° C. Optical rotation: [a]20D = 34.00 (c = 0.10, CH3OH)
The synthesis of tert-butyl methyl(2-(vinylsulfonamido)ethyl)carbamate (153-2)
To a solution of tert-butyl N-(2-aminoethyl)-N-methyl-carbamate (153-1, 500 mg, 2.87 mmol) and TEA (725.93 mg, 7.17 mmol, 999.91 uL) in DCM (10 ml) was added dropwise 2-chloroethanesulfonyl chloride (467.81 mg, 2.87 mmol), the mixture was stirred at room temperature for 1 h and the solvent was removed in vacuo to give 153-2 (750 mg, 98.9% yield) as yellow oil.
The synthesis of N-(2-(methylamino)ethyl)ethenesulfonamide (0153-3)
To a solution of 0153-2 (750 mg, 2.84 mmol) in HCl/dioxane (12 mL) was stirred at room temperature for 2 h, The solvent was removed in vacuo to give 0153-3 (450 mg, 96.6% yield) as yellow oil.
The synthesis of N-(2-(methyl((5-(trifluoromethoxy)-1H-benzo[d]imidazol-2-yl)methyl)amino)ethyl)ethenesulfonamide (SU20667-0153-01)
The solution of 153-3 (125 mg, 761.15 umol), 2-(chloromethyl)-5-(trifluoromethoxy)-1H-benzimidazole (190.75 mg, 761.15 umol), in DMF (3 ml) was added cesium carbonate (248.00 mg, 761.15 umol), the mixture was stirred at room temperature for 3 h, The mixture was filtered and the solution was purified prep-HPLC to give SU20667-0153-01 (73.49 mg, 25.5% yield) as yellow oil. LC-MS (Agilent LCMS 1200-6110, Column: Waters X-Bridge C18 (50 mm*4.6 mm*3.5 µm); Column Temperature: 40° C.; Flow Rate: 2.0 mL/min; Mobile Phase: from 95% [water + 0.05% TFA] and 5% [CH3CN + 0.05% TFA] to 0% [water + 0.05% TFA] and 100% [CH3CN + 0.05 % TFA] in 1.6 min, then under this condition for 1.4 min, finally changed to 95% [water + 0.05% TFA] and 5% [CH3CN + 0.05% TFA] in 0.05 min and under this condition for 0.7 min), Purity: 99.54%, Rt =1.521 min; MS Calcd: 378.37; MS Found: 379.1 [M+H]+. HPLC (Agilent HPLC 1200; Column: L-column2 ODS (150 mm*4.6 mm*5.0 µm); Column Temperature: 40° C.; Flow Rate: 1.0 mL/min; Mobile Phase: from 95% [water + 0.1% TFA] and 5% [CH3CN + 0.1% TFA] to 0% [water + 0.1% TFA] and 100% [CH3CN + 0.1% TFA] in 10 min, then under this condition for 5 min, finally changed to 95% [water + 0.1% TFA] and 5% [CH3CN + 0.1% TFA] in 0.1 min and under this condition for 5 min), Purity: 100.00%, Rt =7.502 min. 1H NMR (400 MHz, DMSO-d6) δ 12.52-12.55 (m, 1 H), 7.43-7.64 (m, 2 H), 7.11-7.22 (m, 2 H), 6.70 (dd, J = 16.8 Hz, 10.0 Hz, 1 H), 6.01 (d, J = 16.8 Hz, 1 H), 5.91 (d, J= 10.0 Hz, 1 H), 3.78 (s, 2 H), 3.00-3.01 (m, 2 H), 2.56-2.57 (m, 2 H), 2.22 (s, 3 H). Chemical Formula: C14H17F3N4O3S. Molecular Weight: 378.37.
The synthesis of sodium 2-oxopropane-1-sulfonate (182-2)
To a solution of 182-1 (500 mg, 3.7 mmol) in H2O (10 mL) was added Na2SO3 (699 mg, 5.55 mmol). The mixture was stirred at rt for 48 h then concentrated in vacuo to give 182-2 (1 g, crude) as a white solid.
The synthesis of 2-oxopropane-1-sulfonyl chloride (182-3)
To a solution of 182-2 (1 g, crude) in toluene (10 mL) was added POCl3 (2 mL). The reaction mixture was stirred at 100° C. for 3 h and concentrated in vacuo, DCM (20 mL) was added and the reaction mixture was filtered, the filtrate was concentrated to give 182-3 (500 mg, crude) as yellow oil.
The synthesis of (R)-3-(2-oxopropylsulfonamido)-N-(4-(trifluoromethoxy)phenyl)piperidine-1-carboxamide (182-4)
To a solution of (R)-3-amino-N-(4-(trifluoromethoxy)phenyl)piperidine-1-carboxamide (496 mg, 1.9 mmol) in DCM (20 mL) was added Et3N (1.15 g, 11.4 mmol) and 182-3 (500 mg, crude). The reaction mixture was stirred at rt for 2 h and quenched with water (20 mL). The organic layer was concentrated and purified by column chromatography (PE/EA= 1:2) to give 182-4 (100 mg, 6.3% three steps) as a white solid.
The synthesis of (R)-3-(prop-1-yn-1-ylsulfonamido)-N-(4-(trifluoromethoxy)phenyl)piperidine-1-carboxamide (SU20667-0182-01)
To a solution of 182-4 (100 mg, 0.23 mmol) in DCM (2 mL) was added DIEA (90 mg, 0.7 mmol) and Tf2O (77 mg, 0.27 mmol). The mixture was stirred at rt for 3 h. The mixture was purified by prep-TLC to give the crude product. The residue was further purified by prep-HPLC to give SU20667-0182-01 (7.29 mg, 7.8%) as a white solid. Agilent LCMS 1200-6120, Column: Waters X-Bridge C18 (50 mm*4.6 mm*3.5 µm); Column Temperature: 40° C.; Flow Rate: 2.0 mL/min; Mobile Phase: from 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] to 0% [water + 10 mM NH4HCO3] and 100% [CH3CN] in 1.6 min, then under this condition for 1.4 min, finally changed to 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] in 0.1 min and under this condition for 0.7 min, Purity 100.00 %, Rt = 1.803 min; MS Calcd.: 405.1; MS Found: 406.1 [M+H]+. Agilent HPLC 1200, Column: Waters X-Bridge C18 (150 mm*4.6 mm*3.5 µm); Column Temperature: 40° C.; Flow Rate: 1.0 mL/min; Mobile Phase: from 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] to 0% [water + 10 mM NH4HCO3] and 100% [CH3CN] in 10 min, then under this condition for 5 min, finally changed to 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] in 0.1 min and under this condition for 5 min, Purity 100.00%, Rt = 8.791 min; MS Calcd.: 405.1; MS Found: 406.1 [M+H]+. 1 H NMR (400 MHz, CD3OD) δ 7.40-7.43 (m, 2 H), 7.15 (d, J = 8.0 Hz, 2 H), 4.09-4.14 (m, 1 H), 3.72-3.76 (m, 1 H), 3.40-3.43 (m, 1 H), 3.14-3.20 (m, 1 H), 3.04-3.09 (m, 1 H), 2.06-2.09 (m, 1 H), 2.04 (s, 3 H), 1.79-1.81 (m, 1 H), 1.58-1.63 (m, 2 H).
The synthesis of 5-fluoro-2-iodo-4-(trifluoromethoxy)aniline (177-2)
To a solution of 3-fluoro-4-(trifluoromethoxy)aniline (3 g, 15.38 mmol) in acetonitrile (50 mL) was added NIS (3.39 g, 15.07 mmol) and stirred at rt for 12 h. Removing the solution and the residue was purified by C.C. (PE/EA= 2:1) to give 177-2 (3.2 g, 9.97 mmol, 64.81% yield) as black oil.
The synthesis of 6-fluoro-5-(trifluoromethoxy)-1H-indole-2-carboxylic acid (177-3)
To a solution of 177-2 (4 g, 12.46 mmol) and 2-oxopropanoic acid (1.21 g, 13.71 mmol) in DMF (60 mL) was added palladium (II) acetate (279.75 mg, 1.25 mmol) and Dabco (2.80 g, 24.92 mmol, 2.45 mL) was stirred at 100° C. for 4 h. Removing the solvent and MeOH was added and filtered, the filtrate was concentrated and used to next step without further purification.
The synthesis of tert-butyl (3S,4R)-4-fluoro-1-(6-fluoro-5-(trifluoromethoxy)-1H-indole-2-carbonyl)piperidin-3-ylcarbamate (0193-2)
To a solution of 177-3 (400 mg, 1.52 mmol) and tert-butyl N-[(3S,4R)-4-fluoro-3-piperidyl]carbamate (331.78 mg, 1.52 mmol) in DCM (6 mL) was added DMAP (278.56 mg, 2.28 mmol) and EDCI (377.43 mg, 1.98 mmol), the mixture was stirred at rt for 2 h, Removing the solvent and the residue was purified by C.C (DCM/MeOH = 15:1) to give 193-2 (450 mg, 971.09 umol, 63.88% yield) as a white solid.
The synthesis of ((3S,4R)-3-amino-4-fluoropiperidin-1-yl)(6-fluoro-5-(trifluoromethoxy)-1H-indol-2-yl)methanone (0193-3)
To a solution of 193-2 (200 mg, 431.59 umol) in HCl/1,4-dioxane (3 mL) was stirred at rt for 1 h, the solvent was removed to give the desired product 193-3 (156 mg, 99.5% yield) as a white solid.
The synthesis of (3S,4R)-4-fluoro-1-((6-fluoro-5-(trifluoromethoxy)-1H-indol-2-yl)methyl)piperidin-3-amine (0193-4)
To a solution of 193-3 (200 mg, 550.54 umol) in THF (2 mL) was added BH3/THF (1.0 N, 2 mL), the mixture was stirred at rt for 2 d. The mixture was pour into ice water and extracted with DCM (20 mL × 3). The organic layer was dried over Na2SO4, filtered and concentrated. The residue was purified by column chromatography (DCM/MeOH= 20:1) to give 193-4 (70 mg, 200.40 umol, 36.40% yield) as colorless oil.
The synthesis of N-((3S,4R)-4-fluoro-1-((6-fluoro-5-(trifluoromethoxy)-1H-indol-2-yl)methyl)piperidin-3-yl)ethenesulfonamide (SU20667-0193-01)
To a solution of 193-4 (70 mg, 200.40 umol) in DCM (2 mL) was added TEA (60.84 mg, 601.21 umol) and 2-chloroethanesulfonyl chloride (32.67 mg, 200.40 umol). The mixture was stirred at rt for 20 min. The mixture was pour into ice water and extracted with DCM (10 mL × 3). The organic layer was dried over Na2SO4, filtered and concentrated. The residue was purified by prep-HPLC to give SU20667-0193-01 (23.16 mg, 26.3% yield) as a white solid. LC-MS (Agilent LCMS 1200-6120, Column: Waters X-Bridge C18 (50 mm*4.6 mm*3.5 µm); Column Temperature: 40° C.; Flow Rate: 2.0 mL/min; Mobile Phase: from 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] to 0% [water + 10 mM NH4HCO3] and 100% [CH3CN] in 1.6 min, then under this condition for 1.4 min, finally changed to 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] in 0.1 min and under this condition for 0.7 min), Purity: 97.25%, Rt =2.147 min; MS Calcd: 439.40; MS Found: 440.2 [M+H]+. HPLC (Agilent HPLC 1200, Column: Waters X-Bridge C18 (150 mm*4.6 mm*3.5 µm); Column Temperature: 40° C.; Flow Rate: 1.0 mL/min; Mobile Phase: from 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] to 0% [water + 10 mM NH4HCO3] and 100% [CH3CN] in 10 min, then under this condition for 5 min, finally changed to 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] in 0.1 min and under this condition for 5 min), Purity:98.90%, Rt =7.331 min. 1H NMR (400 MHz, DMSO-d6) δ 11.38 (s, 1 H), 7.62 (d, J=6.4 Hz, 2 H), 7.34 (d, J=10.8 Hz, 1 H), 6.71 (dd, J=16.4 Hz, J=10.0 Hz, 1 H), 6.37 (s, 1 H), 6.00 (d, J=16.4 Hz, 1 H), 5.82 (d, J=10.0 Hz, 1 H), 4.74 (d, J=47.6 Hz, 1 H), 3.67 (s, 2 H), 3.37-3.38 (m, 1 H), 2.64-2.66 (m, 1 H), 2.49-2.50 (m, 1 H), 2.25-2.32 (m, 2 H), 1.88-1.91 (m, 2 H). Chemical Formula: C17H18F5N3O3S. Molecular Weight: 439.40. Melting point: 165.2-169.9° C.
The synthesis of (R)-tert-butyl 1-(6-fluoro-5-(trifluoromethoxy)-1H-indole-2-carbonyl)piperidin-3-ylcarbamate (177-4)
To a solution of 177-3 (740 mg, 2.81 mmol) and tert-butyl N-[(3R)-3-piperidyl]carbamate (563.21 mg, 2.81 mmol) in DCM (15 mL), was added DMAP (687.12 mg, 5.62 mmol) and EDCI (700.81 mg, 3.66 mmol), the mixture was stirred at rt for 3 h. Removing the solvent and the residue was purified by CC (PE/EA= 2:1) to give 177-4 (600 mg, 47.9% yield) as a yellow solid.
The synthesis of (R)-(3-aminopiperidin-1-yl)(6-fluoro-5-(trifluoromethoxy)-1H-indol-2-yl)methanone (0194-2)
To a solution of 177-4 (150 mg, 336.77 umol) in HCl/1,4-dioxane (3 mL) was stirred at rt for 1 h, the solvent was removed to give the desired product 194-2 (116 mg, 99.76% yield) as a yellow solid.
The synthesis of (R)-N-(1-(6-fluoro-5-(trifluoromethoxy)-1H-indole-2-carbonyl)piperidin-3-yl)ethenesulfonamide (SU20667-0194-01)
To a solution of 194-2(116 mg, 335.95 umol) in DCM (3 mL) was added TEA (140 mg, 1.38 mmol) and 2-chloroethanesulfonyl chloride (54 mg, 331.24 umol). The mixture was stirred at rt for 10 min. The mixture was pour into ice water and extracted with DCM (10 mL× 3). The organic layer was dried over Na2SO4, filtered and concentrated. The residue was purified by prep-HPLC to give SU20667-0194-01 (15.67 mg, 10.7% yield) as a white solid. LC-MS (Agilent LCMS 1200-6120, Column: Waters X-Bridge C18 (50 mm*4.6 mm*3.5 µm); Column Temperature: 40° C.; Flow Rate: 2.0 mL/min; Mobile Phase: from 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] to 0% [water + 10 mM NH4HCO3] and 100% [CH3CN] in 1.6 min, then under this condition for 1.4 min, finally changed to 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] in 0.1 min and under this condition for 0.7 min), Purity: 98.41%, Rt =2.033 min; MS Calcd: 435.39; MS Found: 436.2 [M+H]+. HPLC (Agilent HPLC 1200, Column: Waters X-Bridge C18 (150 mm*4.6 mm*3.5 µm); Column Temperature: 40° C.; Flow Rate: 1.0 mL/min; Mobile Phase: from 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] to 0% [water + 10 mM NH4HCO3] and 100% [CH3CN] in 10 min, then under this condition for 5 min, finally changed to 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] in 0.1 min and under this condition for 5 min), Purity:99.21%, Rt =9.584 min. 1H NMR (400 MHz, DMSO-d6) δ 11.92 (s, 1 H), 7.80 (d, J=6.8 Hz, 1 H), 7.62 (d, J=2.0 Hz, 1 H), 7.39 (d, J=10.0 Hz, 1 H), 6.86 (s, 1 H), 6.76 (dd, J=16.8 Hz, J=9.6 Hz, 1 H), 6.04 (d, J=16.4 Hz, 1 H), 5.90-5.92 (m, 1 H), 4.29-4.32 (m, 1 H), 4.07-4.11 (m, 1 H), 3.16-3.32 (m, 3 H), 1.93-1.95 (m, 1 H), 1.76-1.79 (m, 1 H), 1.46-1.54 (m, 2 H). Chemical Formula: C17H17F4N3O4S. Molecular Weight: 435.39 Melting point: 91.7-98.6° C. Optical rotation: [a]25D = 8.0 (c = 0.20, CH3OH).
The synthesis of sodium 3-methyl-2-oxobutane-1-sulfonate (213-2)
To a solution of 213-1 (1.7 g, 10.3 mmol) in H2O (10 mL) was added Na2SO3 (1.9 g, 15.45 mmol). The mixture was stirred at rt for 48 h and concentrated in vacuo to give 213-2 (2 g, crude) as a white solid.
The synthesis of 3-methyl-2-oxobutane-1-sulfonyl chloride (213-3)
To a solution of 213-2 (2 g, crude) in toluene (20 mL) was added POCl3 (4 mL). The reaction mixture was stirred at 100° C. for 3 h and concentrated in vacuo, DCM (20 mL) was added and the reaction mixture was filtered, the filtrate was concentrated to give 213-3 (1 g, crude) as yellow oil.
The synthesis of (R)-3-(3-methyl-2-oxobutylsulfonamido)-N-(4-(trifluoromethoxy)phenyl)piperidine-1-carboxamide (213-4)
To a solution of (R)-3-amino-N-(4-(trifluoromethoxy)phenyl)piperidine-1-carboxamide (1 g, 4 mmol) in DCM (20 mL) was added Et3 N (2.4 g, 24 mmol) and 213-3 (1 g, crude). The reaction mixture was stirred at rt for 2 h and quenched with water (20 mL). The organic layer was concentrated and purified by column chromatography (PE/EA= 1:2) to give 213-4 (120 mg, 2.6% for three steps) as a white solid.
The synthesis of (R)-3-(3-methylbut-1-yn-1-ylsulfonamido)-N-(4-(trifluoromethoxy)phenyl)piperidine-1-carboxamide (SU20667-0213-01)
To a solution of 213-4 (120 mg, 0.26 mmol) in DCM (2 mL) was added DIEA (103 mg, 0.8 mmol) and Tf2O (88 mg, 0.31 mmol). The mixture was stirred at rt for 3 h. The mixture was purified by prep-TLC to give the crude product. The residue was further purified by prep-HPLC to give SU20667-0213-01 (6.29 mg, 5.5%) as a white solid. Agilent LCMS 1200-6120, Column: Waters X-Bridge C18 (50 mm*4.6 mm*3.5 µm); Column Temperature: 40° C.; Flow Rate: 2.0 mL/min; Mobile Phase: from 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] to 0% [water + 10 mM NH4HCO3] and 100% [CH3CN] in 1.6 min, then under this condition for 1.4 min, finally changed to 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] in 0.1 min and under this condition for 0.7 min, Purity 100.0 %, Rt = 1.621 min; MS Calcd.: 433.1; MS Found: 433.8 [M+H]+. Agilent HPLC 1200, Column: Waters X-Bridge C18 (150 mm*4.6 mm*3.5 µm); Column Temperature: 40° C.; Flow Rate: 1.0 mL/min; Mobile Phase: from 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] to 0% [water + 10 mM NH4HCO3] and 100% [CH3CN] in 10 min, then under this condition for 5 min, finally changed to 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] in 0.1 min and under this condition for 5 min, Purity 100.0%, Rt = 10.380 min; MS Calcd.: 433.1; MS Found: 434.2 [M+H]+. 1 H NMR (400 MHz, DMSO-d6) δ 8.72 (s, 1 H), 8.38 (d, J = 7.2 Hz, 1 H), 7.53-7.55 (m, 2 H), 7.22 (d, J = 8.4 Hz, 2 H), 4.14-4.20 (m, 1 H), 3.82-3.85 (m, 1 H), 3.23-3.34 (m, 1 H), 2.75-2.92 (m, 3 H), 1.98-1.99 (m, 1 H), 1.72-1.74 (m, 1 H), 1.45-1.50 (m, 2 H), 1.16 (d, J = 5.6 Hz, 6 H).
The synthesis of (R)-3-(allylsulfonamido)-N-(4-(trifluoromethoxy)phenyl) piperidine-1-carboxamide (219-1)
To a solution of 219-0 (450 mg, 1.49 mmol) in DCM (10 mL) was added TEA (451 mg, 4.46 mmol), then prop-2-ene-1-sulfonyl chloride (417 mg, 2.98 mmol) was added dropwise at room temperature. Then the mixture was stirred at room temperature for 5 h. Water (30 mL) was added and extracted with DCM (30 mL × 3). The organic layer was dried over Na2SO4, filtered and concentrated to give the oil residue, which was purified by prep-HPLC to give 219-1 (80 mg, 13%) as yellow oil.
The synthesis of (R,E)-3-(4-(dimethylamino)-4-oxobut-2-enylsulfonamido)-N- (4-(trifluoromethoxy)phenyl)piperidine-1-carboxamide (SU20667-0219-01)
To a solution of 219-1 (60 mg, 0.15 mmol) in DCM (5 mL) was added N,N-dimethylacrylamide (18 mg, 0.18 mmol) and Grubb’s second generation catalyst (127 mg, 0.15 mmol). It was stirred at 40° C. for 16 hr. Diluted with water (10 mL) and extracted with DCM (10 mL × 2). The organic layer was dried over Na2SO4, filtered and concentrated. The residue was purified by Prep-HPLC to give SU20667-0219-01 (5 mg, 7%) as a white solid. Agilent LCMS 1200-6120, Column: Waters X-Bridge C18 (50 mm*4.6 mm*3.5 µm); Column Temperature: 40° C.; Flow Rate: 2.0 mL/min; Mobile Phase: from 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] to 0% [water + 10 mM NH4HCO3] and 100% [CH3CN] in 1.6 min, then under this condition for 1.4 min, finally changed to 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] in 0.1 min and under this condition for 0.7 min. Purity is 100%. Rt = 1.877 min; MS Calcd.: 478.2; MS Found: 479.4 [M+H]+. Agilent HPLC 1200, Column: Waters X-Bridge C18 (150 mm*4.6 mm*3.5 µm); Column Temperature: 40° C.; Flow Rate: 1.0 mL/min; Mobile Phase: from 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] to 0% [water + 10 mM NH4HCO3] and 100% [CH3CN] in 10 min, then under this condition for 5 min, finally changed to 95% [water + 10 mM NH4HCO3] and 5% [CH3CN] in 0.1 min and under this condition for 5 min. Purity is 93.7%. Rt = 8.660 min. MS Calcd.: 478.2; MS Found: 479.2 [M+H]+. 1H NMR (400 MHz, DMSO-d6) δ 8.74 (s, 1 H), 7.52 (d, J= 9.2 Hz, 2 H), 7.20 (d, J= 8.8 Hz, 2 H), 6.73 (d, J= 15.2 Hz, 1 H), 6.47-6.57 (m, 1 H), 3.95-4.08 (m, 3 H), 3.77-3.87 (m, 1 H), 3.13-3.22 (m, 1 H), 3.02 (s, 3 H), 2.78-2.88 (m, 5 H), 2.65-2.75 (m, 1 H), 1.86-1.96 (m, 1 H), 1.62-1.75 (m, 1 H), 1.33-1.46 (m, 2 H). Chemical Formula: C19H25F3N4O5S. Molecular Weight: 478.49
tert-Butyl N-(2-{[4-(trifluoromethoxy)phenyl]carbamoyl}ethyl)carbamate (S9): 0.20 mL (1.4 mmol) 4-(trifluoromethoxy)aniline, 0.20 g (1.0 mmol) Boc-β-alanine, 0.23 g (1.2 mmol) 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride and 0.016 g (0.10 mmol) 1-hydroxybenzotriazole hydrate were mixed in 4 mL methylene chloride and stirred overnight. The solution was diluted with 30 mL water and extracted thrice with 25 mL methylene chloride. Flash chromatography using a hexanes/ethyl acetate gradient resulted in 0.33 g of the final product as a white solid in 91% yield. 1H NMR (300 MHz, CDCl3) δ 8.86 (s, 1H), 7.55 (d, J = 8.7 Hz, 2 H), 7.09 (d, J= 8.6 Hz, 2 H), 5.43 (t, J= 6.2 Hz, 1H), 3.45 (q, J= 6.2 Hz, 2 H), 2.57 (t, J = 6.1 Hz, 2 H), 1.39 (s, 9 H). 13C NMR (75 MHz, CDCl3) δ 170.22, 156.68, 145.53, 136.93, 125.76, 122.36, 121.48, 118.96, 115.56, 79.87, 37.68, 36.95, 28.44. Mass (ESI): [M+H-Boc]+ 249.1; found 249.1, [M+acetonitrile+Na]+ 412.1; found 412.1. Rf= 0.40 H:EA 1:1.
3-Ethenesulfonamido-N-[4-(trifluoromethoxy)phenyl]propanamide (11): To 0.33 g (0.95 mmol) tert-butyl N-(2-{[4-(trifluoromethoxy)phenyl]carbamoyl}ethyl)carbamate (S9) in 7 mL methylene chloride was added 2.4 mL (9.5 mmol) 4 M hydrochloric acid in 1,4-dioxane. After 4 hours the solvent was removed using a rotary evaporator. Mass (ESI): [M+H]+ 249.1; found 249.0. Rf = 0.07 DCM:MeOH 9:1. To the crude 3-amino-N-[4-(trifluoromethoxy)phenyl]propanamide in 15 mL of methylene chloride was added 0.66 mL (4.7 mmol) triethylamine followed by 0.50 mL (4.7 mmol) 2-chloroethanesulfonyl chloride. After stirring overnight the solution was diluted with 20 mL water and the aqueous extracted thrice with 10 mL of methylene chloride. Flash chromatography using a hexanes/ethyl acetate gradient resulted in 0.085 g of the final product as a white solid in 27% yield over two steps. 1H NMR (300 MHz, CDCl3) δ 8.30 (s, 1 H), 7.51 (d, J = 8.7 Hz, 2H), 7.09 (d, J = 8.6 Hz, 2 H), 6.49 (dd, J = 16.5, 9.9 Hz, 1 H), 6.19 (d, J = 16.7 Hz, 1H), 5.91 (d, J = 9.9 Hz, 1H), 5.64 (t, J = 6.4 Hz, 1 H), 3.30 (q, J= 6.1 Hz, 2 H), 2.64 (t, J= 6.1 Hz, 2 H). 19F NMR (282 MHz, CDCl3) δ -58.17. 13C NMR (75 MHz, CDCl3) δ 169.77, 145.82, 136.46, 135.92, 126.96, 121.66, 120.69 (q, J=256.8 Hz), 39.33, 37.20. Mass (ESI): [M+H]+ 339.1; found 339.0. Rf = 0.18 H:EA 1:1.
The synthesis of N-[(3 S)-1-[5-(4-Chlorophenyl)furan-2-carbonyl]piperidin-3-yl]ethene-1-sulfonamide.
tert-Butyl N-[(3S)-1-[5-(4-chlorophenyl)furan-2-carbonyl]piperidin-3-yl]carbamate. To a solution of 5-(4-chlorophenyl)furan-2-carboxylic acid (0.16 g, 0.72 mmol) in N,N′-dimethylformamide (1 mL) were added (S)-3-(Boc-amino)piperidine (0.144 g, 0.72 mmol), HATU (0.3 g, 0.79 mmol) and N,N-diisopropylethylamine (0.25 mL, 1.44 mmol). The reaction was stirred at ambient temperature for 2 h then partitioned between ethyl acetate and saturated aqueous ammonium chloride. The layers were separated, and the organic phase was washed with water and brine, dried over MgSO4, filtered, and concentrated. The crude concentrate was purified by flash silica gel chromatography (12 g Silicycle column), eluting with ethyl acetate in hexanes (50%) to provide 0.26 g (89%) of the title compound as an off-white solid. 1H NMR (400 MHz, CHLOROFORM-d, 25° C.): δ = 7.66 (d, J= 7.8 Hz, 2 H), 7.36 (d, J= 8.6 Hz, 2 H), 7.12 (br s, 1 H), 6.69 (d, J= 3.9 Hz, 1 H), 3.80 (br s, 1 H), 3.58 (br s, 1 H), 1.96 (br dd, J= 7.8, 3.5 Hz, 1 H), 1.80 (br s, 1 H), 1.60-1.74 (m, 2 H), 1.51-1.58 (m, 2 H), 1.42-1.48 (m, 1H), 1.39 ppm (s, 9 H). LC-MS: m/z = 427 [M+Na]+.
N-[(3S)-1-[5-(4-Chlorophenyl)furan-2-carbonyl]piperidin-3-yl]ethene-1-sulfonamide. To a solution of tert-butyl N-[(3S)-1-[5-(4-chlorophenyl)furan-2-carbonyl]piperidin-3-yl]carbamate (0.23 g, 0.57 mmol) in dioxane (2.5 mL), was added 4 M solution of hydrochloric acid in dioxane (2.5 mL). The reaction was stirred at ambient temperature for 3 h and then concentrated to dryness to obtain crude (3S)-1-[5-(4-chlorophenyl)furan-2-carbonyl]piperidin-3-amine (~ 0.2 g) as a hydrochloride salt.
The crude (3S)-1-[5-(4-chlorophenyl)furan-2-carbonyl]piperidin-3-amine hydrochloride (0.02 g, 0.059 mmol) was taken in dichloromethane (1 mL) and cooled to 0° C. To this solution, was added 2-chloroethane sulfonyl chloride (6.25 µL, 0.059 mmol) and N,N-diisopropylethylamine (0.02 mL, 0.12 mmol). The mixture was stirred at 0° C. for an hour, followed by addition of N,N-diisopropylethylamine (0.01 mL, 0.06 mmol). The reaction mixture was stirred at 0 ·C and then partitioned between dichloromethane and saturated aqueous ammonium chloride. The layers were separated, and the organic phase was washed with water and brine, dried over MgSO4, filtered, and concentrated. The crude concentrate was purified by flash silica gel chromatography (4 g Silicycle column), eluting with ethyl acetate in hexanes (50%) to provide 0.014 g (61%) of the title compound as a pale yellow solid. 1H NMR (400 MHz, CHLOROFORM-d, 25° C.): δ = 7.64 (br d, J= 8.2 Hz, 2 H), 7.38 (br d, J= 8.6 Hz, 2H), 7.09-7.11 (m, 1 H), 6.71 (br d, J= 3.5 Hz, 1 H), 6.49-6.58 (m, 1 H), 6.25 (br d, J= 16.4 Hz, 1 H), 5.89 (br d, J= 9.8 Hz, 1 H), 3.81 (br s, 1 H), 3.62-3.75 (m, 2 H), 3.53 (br s, 1 H), 1.95-2.06 (m, 1 H), 1.75-1.92 (m, 1 H), 1.61-1.74 (m, 1 H), 1.21-1.39 ppm (m, 2 H). LC-MS: m/z = 395 [M+H]+.
Synthesis of 5-(4-Chlorophenyl)-N-methyl-N-[2-(N-methylethenesulfonamido)ethyl]furan-2-carboxamide.
tert-Butyl N-(2-{1-[5-(4-chlorophenyl)furan-2-yl]-N-methylformamido}ethyl)-N-methylcarbamate. To a solution of 5-(4-chlorophenyl)furan-2-carboxylic acid (0.1 g, 0.45 mmol) in N,N′-dimethylformamide (0.5 mL) were added tert-butyl N-methyl-N-[2-(methylamino)ethyl]carbamate (0.085 g, 0.45 mmol), HATU (0.19 g, 0.5 mmol) and N,N-diisopropylethylamine (0.16 mL, 0.9 mmol). The reaction was stirred at ambient temperature for 18 h then partitioned between ethyl acetate and saturated aqueous ammonium chloride. The layers were separated, and the organic phase was washed with water and brine, dried over MgSO4, filtered, and concentrated. The crude concentrate was purified by flash silica gel chromatography (12 g Silicycle column), eluting with ethyl acetate in hexanes (50%) to provide 0.17 g (96%) of the title compound as pale yellow oil. 1H NMR (400 MHz, CHLOROFORM-d, 27° C.): δ = 7.65 (br d, J= 7.3 Hz, 2H), 7.40 (br d, J= 8.3 Hz, 2 H), 7.15 (br s, 1 H), 6.73 (br s, 1 H), 3.74 (br s, 1 H), 3.53 (br t, J = 5.7 Hz, 2 H), 3.44 (br s, 1 H), 2.94 (br s, 2 H), 1.43 (br s, 9H). LC-MS: m/z = 393 [M+H]+.
5-(4-Chlorophenyl)-N-methyl-N-[2-(N-methylethenesulfonamido)ethyl]furan-2-carboxamide. To a solution of tert-butyl N-(2-{ 1-[5-(4-chlorophenyl)furan-2-yl]-N-methylformamido}ethyl)-N-methylcarbamate (0.018 g, 0.046 mmol) in dioxane (0.2 mL), was added 4 M solution of hydrochloric acid in dioxane (0.2 mL). The reaction was stirred at 0° C. for 2 h and then concentrated to dryness to obtain crude 5-(4-chlorophenyl)-N-methyl-N-[2-(methylamino)ethyl]furan-2-carboxamide as a hydrochloride salt.
The crude 5-(4-chlorophenyl)-N-methyl-N-[2-(methylamino)ethyl]furan-2-carboxamide hydrochloride was taken in dichloromethane (0.5 mL) and cooled to 0° C. To this solution, was added 2-chloroethane sulfonyl chloride (5 µL, 0.046 mmol) and N,N-diisopropylethylamine (16 µL, 0.092 mmol). The mixture was stirred at 0° C. for an hour, followed by addition of N,N-diisopropylethylamine (8 µL, 0.046 mmol). The reaction mixture was stirred at 0 ·C and concentrated. The crude concentrate was purified by flash silica gel chromatography (4 g Silicycle column), eluting with ethyl acetate in hexanes (50-100%) to provide 5 mg (29%) of the title compound as a pale yellow solid. 1H NMR (400 MHz, CHLOROFORM-d, 27° C.): δ = 7.61-7.71 (m, 2 H), 7.37-7.47 (m, 2 H), 7.16 (br d, J = 3.2 Hz, 1 H), 6.75 (d, J= 3.7 Hz, 1H), 6.45 (dd, J= 16.6, 10.0 Hz, 1 H), 6.25 (d, J= 16.6 Hz, 1 H), 5.99 (d, J= 10.0 Hz, 1 H), 3.80 (br dd, J= 5.1, 1.2 Hz, 2 H), 3.35-3.55 (m, 5 H), 2.80-2.99 ppm (m, 3 H). LC-MS: m/z = 405 [M+Na]+.
Synthesis of 5-(4-Chlorophenyl)-N-(2-ethenesulfonamidoethyl)furan-2-carboxamide
tert-Butyl N-(2-{[5-(4-chlorophenyl)furan-2-yl]formamido}ethyl)carbamate. To a solution of 5-(4-chlorophenyl)furan-2-carboxylic acid (0.25 g, 1.12 mmol) in N,N′-dimethylformamide (1.0 mL) were added tert-butyl N-(2-aminoethyl)carbamate (0.18 mL, 1.12 mmol), HATU (0.47 g, 1.23 mmol) and N,N-diisopropylethylamine (0.39 mL, 2.24 mmol). The reaction was stirred at ambient temperature for 18 h then partitioned between ethyl acetate and saturated aqueous ammonium chloride. The layers were separated, and the organic phase was washed with water and brine, dried over MgSO4, filtered, and concentrated. The crude concentrate was purified by flash silica gel chromatography (25 g Silicycle column), eluting with ethyl acetate in hexanes (50%) to provide 0.33 g (81%) of the title compound as cream colored solid. 1H NMR (400 MHz, CHLOROFORM-d, 27° C.): δ = 7.74 (br d, J= 8.3 Hz, 2 H), 7.52 (br s, 1 H), 7.40 (d, J = 8.5 Hz, 2 H), 7.18 (d, J = 3.4 Hz, 1 H), 6.74 (d, J = 3.4 Hz, 1 H), 5.01 (br s, 1 H), 3.58 (q, J= 5.2 Hz, 2 H), 3.44 (br d, J= 4.9 Hz, 2 H), 1.46 ppm (s, 9 H). LC-MS: m/z = 365 [M+H]+.
5-(4-Chlorophenyl)-N-(2-ethenesulfonamidoethyl)furan-2-carboxamide. To a solution of tert-butyl N-(2-{[5-(4-chlorophenyl)furan-2-yl]formamido}ethyl)carbamate (0.027 g, 0.074 mmol) in dioxane (0.3 mL), was added 4 M solution of hydrochloric acid in dioxane (0.3 mL). The reaction was stirred at 0° C. for 2 h and then concentrated to dryness to obtain crude N-(2-aminoethyl)-5-(4-chlorophenyl)furan-2-carboxamide as a hydrochloride salt.
The crude N-(2-aminoethyl)-5-(4-chlorophenyl)furan-2-carboxamide hydrochloride was taken in dichloromethane (0.5 mL) and cooled to 0° C. To this solution, was added 2-chloroethane sulfonyl chloride (8 µL, 0.046 mmol) and N,N-diisopropylethylamine (26 µL, 0.14 mmol). The mixture was stirred at 0° C. for an hour, followed by addition of N,N-diisopropylethylamine (13 µL, 0.07 mmol). The reaction mixture was stirred at 0° C. and concentrated. The crude concentrate was purified by flash silica gel chromatography (4 g Silicycle column), eluting with ethyl acetate in hexanes (50-100%) to provide 10 mg (38%) of the title compound as a clear oil. 1H NMR (400 MHz, CHLOROFORM-d, 27° C.): δ = 7.69 (d, J = 8.5 Hz, 2 H), 7.43 (d, J= 8.8 Hz, 2 H), 7.17-7.25 (m, 1 H), 6.94 (br s, 1 H), 6.76 (d, J= 3.4 Hz, 1 H), 6.50-6.62 (m, 1 H), 6.23-6.37 (m, 1 H), 5.98 (d, J= 10.0 Hz, 1 H), 3.64-3.68 (m, 2 H), 3.32-3.36 (m, 2 H). LC-MS: m/z = 377 [M+Na]+.
tion at which 50% of the subunit is bound to compound, based on mass spectrometry. b for biochemical assay, see Heise, et al. PLoS One, 2012, 7, e50864.
a SS and LS refer to the short subunit and large subunit of caspase-6; DR50 refers to the concentration at which 50% of the subunit is bound to compound, based on mass spectrometry. b for biochemical assay, see Heise, et al. PLoS One, 2012, 7, e50864.
Scheme 19: Caspase 6 IC50 data (nM) for select compounds. For assay method, see Heise, et al. PLoS One, 2012, 7, e50864.
Scheme 19 (cont).
The synthesis of sulfoximines (e.g.
) and sulfondiimines (
) can be carried out according to methods known to one of skill in the art, including but not limited to those methods reported Org. Chem. Front., 2019, 6, 1319-1324.
This application claims the benefit of U.S. Provisional Application No. 62/939,263, filed Nov. 22, 2019, which is incorporated herein by reference in its entirety and for all purposes. The Sequence Listing written in file 048536-664001WO_Sequence_Listing_ST25.txt, created Nov. 16, 2020, 9,466 bytes, machine format IBM-PC, MS Windows operating system, is hereby incorporated by reference.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/US2020/061659 | 11/20/2020 | WO |
| Number | Date | Country | |
|---|---|---|---|
| 62939263 | Nov 2019 | US |
