SUBSTITUTED NUCLEOSIDES, NUCLEOTIDES AND ANALOGS THEREOF

INCORPORATION BY REFERENCE TO ANY PRIORITY APPLICATIONS

[0001] Any and all applications for which a foreign or domestic priority claim is identified in the Application Data Sheet as filed with the present application, are hereby incorporated by reference under 37 CFR 1.57.

REFERENCE TO SEQUENCE LISTING

[0002] The present application is being filed along with a Sequence Listing in electronic format. The Sequence Listing is provided as a file entitled SEQLISTING_067.TXT, created December 19, 2013, which is 728 bytes in size. The information in the electronic format of the Sequence Listing is incorporated herein by reference in its entirety.

BACKGROUND

Field

[0003] The present application relates to the fields of chemistry, biochemistry and medicine. More particularly, disclosed herein are nucleotide analogs, pharmaceutical compositions that include one or more nucleotide analogs and methods of synthesizing the same. Also disclosed herein are methods of treating diseases and/or conditions with a nucleotide analog, alone or in combination therapy with one or more other agents.

Description

[0004] Nucleoside analogs are a class of compounds that have been shown to exert antiviral and anticancer activity both in vitro and in vivo, and thus, have been the subject of widespread research for the treatment of viral infections. Nucleoside analogs are usually therapeutically inactive compounds that are converted by host or viral enzymes to their respective active anti-metabolites, which, in turn, may inhibit polymerases involved in viral or cell proliferation. The activation occurs by a variety of mechanisms, such as the addition of one or more phosphate groups and, or in combination with, other metabolic processes.

SUMMARY

[0005] Some embodiments disclosed herein relate to a compound of Formula (I) or a pharmaceutically acceptable salt thereof. [0006] Some embodiments disclosed herein relate to a method of ameliorating and/or treating a hepatitis C viral (HCV) infection that can include administering to a subject identified as suffering from the HCV infection a therapeutically effective amount of one or more compounds of Formula (I), or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition that includes one or more compounds of Formula (I), or a pharmaceutically acceptable salt thereof. Other embodiments described herein relate to using one or more compounds of Formula (I), or a pharmaceutically acceptable salt thereof, in the manufacture of a medicament for ameliorating and/or treating a HCV infection. Still other embodiments described herein relate to one or more compounds of Formula (I), or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition that includes one or more compounds of Formula (I), or a pharmaceutically acceptable salt thereof, that can be used for ameliorating and/or treating a HCV infection.

[0007] Some embodiments disclosed herein relate to a method of ameliorating and/or treating a HCV infection that can include contacting a cell infected with the hepatitis C virus with an effective amount of one or more compounds described herein, or a pharmaceutically acceptable salt of one or more compounds described herein, or a pharmaceutical composition that includes one or more compounds described herein, or a pharmaceutically acceptable salt thereof. Other embodiments described herein relate to using one or more compounds described herein, or a pharmaceutically acceptable salt of one or more compounds described herein, in the manufacture of a medicament for ameliorating and/or treating a HCV infection that can include contacting a cell infected with the hepatitis C virus with an effective amount of said compound(s). Still other embodiments described herein relate to one or more compounds described herein, or a pharmaceutically acceptable salt of one or more compounds described herein, or a pharmaceutical composition that includes one or more compounds described herein, or a pharmaceutically acceptable salt thereof, that can be used for ameliorating and/or treating a HCV infection by contacting a cell infected with the hepatitis C virus with an effective amount of said compound(s).

[0008] Some embodiments disclosed herein relate to a method of inhibiting replication of a hepatitis C virus that can include contacting a cell infected with the hepatitis C virus with an effective amount of one or more compounds described herein, or a pharmaceutically acceptable salt of one or more compounds described herein, or a pharmaceutical composition that includes one or more compounds described herein, or a pharmaceutically acceptable salt thereof. Other embodiments described herein relate to using one or more compounds described herein, or a pharmaceutically acceptable salt of one or more compounds described herein, in the manufacture of a medicament for inhibiting replication of a hepatitis C virus that can include contacting a cell infected with the hepatitis C virus with an effective amount of said compound(s). Still other embodiments described herein relate to one or more compounds described herein, or a pharmaceutically acceptable salt of one or more compounds described herein, or a pharmaceutical composition that includes one or more compounds described herein, or a pharmaceutically acceptable salt thereof, that can be used for inhibiting replication of a hepatitis C virus by contacting a cell infected with the hepatitis C virus with an effective amount of said compound(s).

[0009] Some embodiments disclosed herein relate to a method of ameliorating and/or treating a HCV infection that can include administering to a subject identified as suffering from the HCV infection a therapeutically effective amount of a compound described herein or a pharmaceutically acceptable salt thereof (for example, one or more compounds of Formula (I), or a pharmaceutically acceptable salt thereof), or a pharmaceutical composition that includes a compound described herein, or a pharmaceutically acceptable salt thereof, in combination with an agent selected from an interferon, ribavirin, a HCV protease inhibitor, a HCV polymerase inhibitor, a NS5A inhibitor, an other antiviral compound, a compound of Formula (AA), a compound of Formula (BB) and a compound of Formula (CC), or a pharmaceutically acceptable salt of any of the foregoing. Some embodiments disclosed herein relate to a method of ameliorating and/or treating a HCV infection that can include contacting a cell infected with the HCV infection with a therapeutically effective amount of a compound described herein or a pharmaceutically acceptable salt thereof (for example, one or more compounds of Formula (I), or a pharmaceutically acceptable salt thereof), or a pharmaceutical composition that includes a compound described herein, in combination with an agent selected from an interferon, ribavirin, a HCV protease inhibitor, a HCV polymerase inhibitor, a NS5A inhibitor, an other antiviral compound, a compound of Formula (AA), a compound of Formula (BB) and a compound of Formula (CC), or a pharmaceutically acceptable salt of any of the foregoing. Some embodiments disclosed herein relate to a method of inhibiting replication of a hepatitis C virus that can include administering to a subject identified as suffering from a HCV infection a therapeutically effective amount of a compound described herein or a pharmaceutically acceptable salt thereof (for example, a compound of Formula (I), or a pharmaceutically acceptable salt thereof), or a pharmaceutical composition that includes a compound described herein, or a pharmaceutically acceptable salt thereof, in combination with an agent selected from an interferon, ribavirin, a HCV protease inhibitor, a HCV polymerase inhibitor, a NS5A inhibitor, an other antiviral compound, a compound of Formula (AA), a compound of Formula (BB) and a compound of Formula (CC), or a pharmaceutically acceptable salt of any of the foregoing. In some embodiments, the agent can be a compound, or a pharmaceutically acceptable salt thereof, selected from Compound 1001-1016, 2001-2012, 3001-3014, 4001- 4012, 5001-5012, 6001-6078, 7000-7027 and 8000-8016, or a pharmaceutical composition that includes one or more of the aforementioned compounds, or a pharmaceutically acceptable salt of the foregoing. In some embodiments, the method can include administering a second agent selected from an interferon, ribavirin, a HCV protease inhibitor, a HCV polymerase inhibitor, a NS5A inhibitor, an other antiviral compound, a compound of Formula (AA), a compound of Formula (BB) and a compound of Formula (CC), or a pharmaceutically acceptable salt of any of the foregoing.

BRIEF DESCRIPTION OF THE DRAWINGS

[0010] Figure 1 shows example HCV protease inhibitors.

[0011] Figure 2 shows example nucleoside HCV polymerase inhibitors.

[0012] Figure 3 shows example non-nucleoside HCV polymerase inhibitors.

[0013] Figure 4 shows example NS5A inhibitors.

[0014] Figure 5 shows example other antivirals.

[0015] Figure 6 shows example compounds of Formula (CC) and alpha- thiotriphosphates thereof, wherein Formula (CC) and alpha-thiotriphosphates thereof are described herein.

[0016] Figure 7 shows example compounds of Formula (AA), wherein Formula (AA) is described herein.

[0017] Figure 8 shows example compounds of Formula (BB) , wherein Formula (BB) is described herein.

[0018] Figure 9 shows example compounds of Formula (I) , wherein Formula (I) is described herein.

[0019] Figure 10 shows the gels from the assessment of incorporation of several compounds with a guanine base by the human mitochondrial RNA polymerase.

[0020] Figure 11 shows the results of the inhibition of mitochondrial protein synthesis assays. DETAILED DESCRIPTION

Definitions

[0021] Unless defined otherwise, all technical and scientific terms used herein have the same meaning as is commonly understood by one of ordinary skill in the art. All patents, applications, published applications and other publications referenced herein are incorporated by reference in their entirety unless stated otherwise. In the event that there are a plurality of definitions for a term herein, those in this section prevail unless stated otherwise.

[0022] As used herein, any "R" group(s) such as, without limitation, R ¹ , R ² , R ³ , R ^4A ,

Tj 4B _R 5 _R 6 _R 7 _R 8 Tj 9A τ} 9Β _r 9C _R 10 _R ll _R 12 _R 13 _R 14 _R 15 _R 16 _R 17 _R 18 _R 19 _R 20 _R 21 _R 22 l\ , Jv , Jv _; Jv , Jv , Jv , rv , rv , rv , rv , rv , rv , rv , rv , rv , rv , rv , rv , rv , rv , rv ,

R ^A1 , R ^A2 , R ^A3 and R ^A4 represent substituents that can be attached to the indicated atom. An R group may be substituted or unsubstituted. If two "R" groups are described as being "taken together" the R groups and the atoms they are attached to can form a cycloalkyl, cycloalkenyl, aryl, heteroaryl or heterocycle. For example, without limitation, if R ^a and R ^b of an NR ^a R ^b group are indicated to be "taken together," it means that they are covalently bonded to one another to form a ring:

— < \

In addition, if two "R" groups are described as being "taken together" with the atom(s) to which they are attached to form a ring as an alternative, the R groups are not limited to the variables or substituents defined previously.

[0023] Whenever a group is described as being "optionally substituted" that group may be unsubstituted or substituted with one or more of the indicated substituents. Likewise, when a group is described as being "unsubstituted or substituted" if substituted, the substituent(s) may be selected from one or more the indicated substituents. If no substituents are indicated, it is meant that the indicated "optionally substituted" or "substituted" group may be substituted with one or more group(s) individually and independently selected from alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl, heteroaryl, heteroalicyclyl, aralkyl, heteroaralkyl, (heteroalicyclyl)alkyl, hydroxy, alkoxy, aryloxy, acyl, mercapto, alkylthio, arylthio, cyano, halogen, thiocarbonyl, O-carbamyl, N-carbamyl, O-thiocarbamyl, N-thiocarbamyl, C-amido, N-amido, S-sulfonamido, N-sulfonamido, C-carboxy, O-carboxy, isocyanato, thiocyanato, isothiocyanato, nitro, silyl, sulfenyl, sulfinyl, sulfonyl, haloalkyl, haloalkoxy, trihalomethanesulfonyl, trihalomethanesulfonamido, an amino, a mono-substituted amino group and a di-substituted amino group. [0024] As used herein, "C _a to C _b " in which "a" and "b" are integers refer to the number of carbon atoms in an alkyl, alkenyl or alkynyl group, or the number of carbon atoms in the ring of a cycloalkyl, cycloalkenyl, aryl, heteroaryl or heteroalicyclyl group. That is, the alkyl, alkenyl, alkynyl, ring of the cycloalkyl, ring of the cycloalkenyl, ring of the aryl, ring of the heteroaryl or ring of the heteroalicyclyl can contain from "a" to "b", inclusive, carbon atoms. Thus, for example, a "Ci to C ₄ alkyl" group refers to all alkyl groups having from 1 to 4 carbons, that is, CH ₃ -, CH ₃ CH ₂ -, CH ₃ CH ₂ CH ₂ -, (CH ₃ ) ₂ CH-, CH ₃ CH ₂ CH ₂ CH ₂ -, CH ₃ CH ₂ CH(CH ₃ )- and (CH ₃ ) ₃ C-. If no "a" and "b" are designated with regard to an alkyl, alkenyl, alkynyl, cycloalkyl cycloalkenyl, aryl, heteroaryl or heteroalicyclyl group, the broadest range described in these definitions is to be assumed.

[0025] As used herein, "alkyl" refers to a straight or branched hydrocarbon chain that comprises a fully saturated (no double or triple bonds) hydrocarbon group. The alkyl group may have 1 to 20 carbon atoms (whenever it appears herein, a numerical range such as "1 to 20" refers to each integer in the given range; e.g., "1 to 20 carbon atoms" means that the alkyl group may consist of 1 carbon atom, 2 carbon atoms, 3 carbon atoms, etc., up to and including 20 carbon atoms, although the present definition also covers the occurrence of the term "alkyl" where no numerical range is designated). The alkyl group may also be a medium size alkyl having 1 to 10 carbon atoms. The alkyl group could also be a lower alkyl having 1 to 6 carbon atoms. The alkyl group of the compounds may be designated as "Ci-C ₄ alkyl" or similar designations. By way of example only, "C ₁ -C ₄ alkyl" indicates that there are one to four carbon atoms in the alkyl chain, i.e., the alkyl chain is selected from methyl, ethyl, propyl, iso-propyl, n-butyl, iso-butyl, sec -butyl and t-butyl. Typical alkyl groups include, but are in no way limited to, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tertiary butyl, pentyl and hexyl. The alkyl group may be substituted or unsubstituted.

[0026] As used herein, "alkenyl" refers to an alkyl group that contains in the straight or branched hydrocarbon chain one or more double bonds. An alkenyl group may be unsubstituted or substituted.

[0027] As used herein, "alkynyl" refers to an alkyl group that contains in the straight or branched hydrocarbon chain one or more triple bonds. An alkynyl group may be unsubstituted or substituted.

[0028] As used herein, "cycloalkyl" refers to a completely saturated (no double or triple bonds) mono- or multi- cyclic hydrocarbon ring system. When composed of two or more rings, the rings may be joined together in a fused fashion. Cycloalkyl groups can contain 3 to 10 atoms in the ring(s) or 3 to 8 atoms in the ring(s). A cycloalkyl group may be unsubstituted or substituted. Typical cycloalkyl groups include, but are in no way limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and cyclooctyl.

[0029] As used herein, "cycloalkenyl" refers to a mono- or multi- cyclic hydrocarbon ring system that contains one or more double bonds in at least one ring; although, if there is more than one, the double bonds cannot form a fully delocalized pi-electron system throughout all the rings (otherwise the group would be "aryl," as defined herein). When composed of two or more rings, the rings may be connected together in a fused fashion. A cycloalkenyl can contain 3 to 10 atoms in the ring(s) or 3 to 8 atoms in the ring(s). A cycloalkenyl group may be unsubstituted or substituted.

[0030] As used herein, "aryl" refers to a carbocyclic (all carbon) monocyclic or multicyclic aromatic ring system (including fused ring systems where two carbocyclic rings share a chemical bond) that has a fully delocalized pi-electron system throughout all the rings. The number of carbon atoms in an aryl group can vary. For example, the aryl group can be a C6-C14 aryl group, a C6-C1 ₀ aryl group, or a Ce aryl group. Examples of aryl groups include, but are not limited to, benzene, naphthalene and azulene. An aryl group may be substituted or unsubstituted.

[0031] As used herein, "heteroaryl" refers to a monocyclic, bicyclic and tricyclic aromatic ring system (a ring system with fully delocalized pi-electron system) that contain(s) one or more heteroatoms (for example, 1 to 5 heteroatoms), that is, an element other than carbon, including but not limited to, nitrogen, oxygen and sulfur. The number of atoms in the ring(s) of a heteroaryl group can vary. For example, the heteroaryl group can contain 4 to 14 atoms in the ring(s), 5 to 10 atoms in the ring(s) or 5 to 6 atoms in the ring(s). Furthermore, the term "heteroaryl" includes fused ring systems where two rings, such as at least one aryl ring and at least one heteroaryl ring, or at least two heteroaryl rings, share at least one chemical bond. Examples of heteroaryl rings include, but are not limited to, furan, furazan, thiophene, benzothiophene, phthalazine, pyrrole, oxazole, benzoxazole, 1,2,3-oxadiazole, 1,2,4-oxadiazole, thiazole, 1 ,2,3-thiadiazole, 1 ,2,4-thiadiazole, benzothiazole, imidazole, benzimidazole, indole, indazole, pyrazole, benzopyrazole, isoxazole, benzoisoxazole, isothiazole, triazole, benzotriazole, thiadiazole, tetrazole, pyridine, pyridazine, pyrimidine, pyrazine, purine, pteridine, quinoline, isoquinoline, quinazoline, quinoxaline, cinnoline and triazine. A heteroaryl group may be substituted or unsubstituted.

[0032] As used herein, "heterocyclyl" or "heteroalicyclyl" refers to three-, four-, five-, six-, seven-, eight-, nine-, ten-, up to 18-membered monocyclic, bicyclic and tricyclic ring system wherein carbon atoms together with from 1 to 5 heteroatoms constitute said ring system. A heterocycle may optionally contain one or more unsaturated bonds situated in such a way, however, that a fully delocalized pi-electron system does not occur throughout all the rings. The heteroatom(s) is an element other than carbon including, but not limited to, oxygen, sulfur and nitrogen. A heterocycle may further contain one or more carbonyl or thiocarbonyl functionalities, so as to make the definition include oxo-systems and thio-systems such as lactams, lactones, cyclic imides, cyclic thioimides and cyclic carbamates. When composed of two or more rings, the rings may be joined together in a fused fashion. Additionally, any nitrogens in a heteroalicyclic may be quaternized. Heterocyclyl or heteroalicyclic groups may be unsubstituted or substituted. Examples of such "heterocyclyl" or "heteroalicyclyl" groups include but are not limited to, 1,3-dioxin, 1,3-dioxane, 1,4-dioxane, 1,2-dioxolane, 1,3- dioxolane, 1,4-dioxolane, 1,3-oxathiane, 1,4-oxathiin, 1,3-oxathiolane, 1,3-dithiole, 1,3- dithiolane, 1,4-oxathiane, tetrahydro- 1 ,4-thiazine, 2H-l,2-oxazine, maleimide, succinimide, barbituric acid, thiobarbituric acid, dioxopiperazine, hydantoin, dihydrouracil, trioxane, hexahydro-l,3,5-triazine, imidazoline, imidazolidine, isoxazoline, isoxazolidine, oxazoline, oxazolidine, oxazolidinone, thiazoline, thiazolidine, morpholine, oxirane, piperidine N-Oxide, piperidine, piperazine, pyrrolidine, pyrrolidone, pyrrolidione, 4-piperidone, pyrazoline, pyrazolidine, 2-oxopyrrolidine, tetrahydropyran, 4H-pyran, tetrahydrothiopyran, thiamorpholine, thiamorpholine sulfoxide, thiamorpholine sulfone and their benzo-fused analogs (e.g., benzimidazolidinone, tetrahydroquinoline and 3,4-methylenedioxyphenyl).

[0033] As used herein, "aralkyl" and "aryl(alkyl)" refer to an aryl group connected, as a substituent, via a lower alkylene group. The lower alkylene and aryl group of an aralkyl may be substituted or unsubstituted. Examples include but are not limited to benzyl, 2- phenylalkyl, 3-phenylalkyl and naphthylalkyl.

[0034] As used herein, "heteroaralkyl" and "heteroaryl(alkyl)" refer to a heteroaryl group connected, as a substituent, via a lower alkylene group. The lower alkylene and heteroaryl group of heteroaralkyl may be substituted or unsubstituted. Examples include but are not limited to 2-thienylalkyl, 3-thienylalkyl, furylalkyl, thienylalkyl, pyrrolylalkyl, pyridylalkyl, isoxazolylalkyl, imidazolylalkyl and their benzo-fused analogs.

[0035] A "(heteroalicyclyl)alkyl" and "(heterocyclyl)alkyl" refer to a heterocyclic or a heteroalicyclylic group connected, as a substituent, via a lower alkylene group. The lower alkylene and heterocyclyl of a (heteroalicyclyl)alkyl may be substituted or unsubstituted. Examples include but are not limited tetrahydro-2H-pyran-4-yl)methyl, (piperidin-4-yl)ethyl, (piperidin-4-yl)propyl, (tetrahydro-2H-thiopyran-4-yl)methyl and (l,3-thiazinan-4-yl)methyl. [0036] "Lower alkylene groups" are straight-chained -CH ₂ - tethering groups, forming bonds to connect molecular fragments via their terminal carbon atoms. Examples include but are not limited to methylene (-(¾-), ethylene (-CH ₂ CH ₂ -), propylene (- CH ₂ CH ₂ CH ₂ -) and butylene (-CH ₂ CH ₂ CH ₂ CH ₂ -). A lower alkylene group can be substituted by replacing one or more hydrogen of the lower alkylene group with a substituent(s) listed under the definition of "substituted."

[0037] As used herein, "alkoxy" refers to the formula -OR wherein R is an alkyl, an alkenyl, an alkynyl, a cycloalkyl, a cycloalkenyl, aryl, heteroaryl, heteroalicyclyl, aralkyl, (heteroaryl)alkyl or (heteroalicyclyl)alkyl is defined herein. A non-limiting list of alkoxys are methoxy, ethoxy, n-propoxy, 1-methylethoxy (isopropoxy), n-butoxy, iso-butoxy, sec-butoxy, tert-butoxy, phenoxy and benzoxy. An alkoxy may be substituted or unsubstituted.

[0038] As used herein, "acyl" refers to a hydrogen, alkyl, alkenyl, alkynyl, or aryl connected, as substituents, via a carbonyl group. Examples include formyl, acetyl, propanoyl, benzoyl and acryl. An acyl may be substituted or unsubstituted.

[0039] As used herein, "hydroxyalkyl" refers to an alkyl group in which one or more of the hydrogen atoms are replaced by a hydroxy group. Exemplary hydroxyalkyl groups include but are not limited to, 2 -hydroxy ethyl, 3-hydroxypropyl, 2-hydroxypropyl and 2,2- dihydroxy ethyl. A hydroxyalkyl may be substituted or unsubstituted.

[0040] As used herein, "haloalkyl" refers to an alkyl group in which one or more of the hydrogen atoms are replaced by a halogen (e.g., mono-haloalkyl, di-haloalkyl and tri- haloalkyl). Such groups include but are not limited to, chloromethyl, fluoromethyl, difluoromethyl, trifluoromethyl, 1 -chloro-2-fluoromethyl and 2-fluoroisobutyl. A haloalkyl may be substituted or unsubstituted.

[0041] As used herein, "haloalkoxy" refers to an -O-alkyl group in which one or more of the hydrogen atoms are replaced by a halogen (e.g., mono-haloalkoxy, di- haloalkoxy and tri- haloalkoxy). Such groups include but are not limited to, chloromethoxy, fluoromethoxy, difluoromethoxy, trifluoromethoxy, 1 -chloro-2-fluoromethoxy and 2-fluoroisobutoxy. A haloalkoxy may be substituted or unsubstituted.

[0042] As used herein, "arylthio" refers to RS-, in which R is an aryl, such as, but not limited to, phenyl. An arylthio may be substituted or unsubstituted.

[0043] A "sulfenyl" group refers to an "-SR" group in which R can be hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl, heteroaryl, heteroalicyclyl, aralkyl, (heteroaryl)alkyl or (heteroalicyclyl)alkyl. A sulfenyl may be substituted or unsubstituted. [0044] A "sulfinyl" group refers to an "-S(=0)-R" group in which R can be the same as defined with respect to sulfenyl. A sulfinyl may be substituted or unsubstituted.

[0045] A "sulfonyl" group refers to an "SO2R" group in which R can be the same as defined with respect to sulfenyl. A sulfonyl may be substituted or unsubstituted.

[0046] An "O-carboxy" group refers to a "RC(=0)0-" group in which R can be hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl, heteroaryl, heteroalicyclyl, aralkyl, (heteroaryl)alkyl or (heteroalicyclyl)alkyl, as defined herein. An O-carboxy may be substituted or unsubstituted.

[0047] The terms "ester" and "C-carboxy" refer to a "-C(=0)OR" group in which R can be the same as defined with respect to O-carboxy. An ester and C-carboxy may be substituted or unsubstituted.

[0048] A "thiocarbonyl" group refers to a "-C(=S)R" group in which R can be the same as defined with respect to O-carboxy. A thiocarbonyl may be substituted or unsubstituted.

[0049] A "trihalomethanesulfonyl" group refers to an "X3CSO2-" group wherein each X is a halogen.

[0050] A "trihalomethanesulfonamido" group refers to an "X ₃ CS(0)2N(RA)-" group wherein each X is a halogen, and RA is hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl, heteroaryl, heteroalicyclyl, aralkyl, (heteroaryl)alkyl or

(heteroalicyclyl)alkyl.

[0051] The term "amino" as used herein refers to a -NH ₂ group.

[0052] As used herein, the term "hydroxy" refers to a -OH group.

[0053] A "cyano" group refers to a "-CN" group.

[0054] The term "azido" as used herein refers to a -N3 group.

[0055] An "isocyanato" group refers to a "-NCO" group.

[0056] A "thiocyanato" group refers to a "-CNS" group.

[0057] An "isothiocyanato" group refers to an " -NCS" group.

[0058] A "mercapto" group refers to an "-SH" group.

[0059] A "carbonyl" group refers to a C=0 group.

[0060] An "S-sulfonamido" group refers to a "-S02 (RARB)" group in which R _A and

RB can be independently hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl, heteroaryl, heteroalicyclyl, aralkyl, (heteroaryl)alkyl or (heteroalicyclyl)alkyl. An S-sulfonamido may be substituted or unsubstituted.

[0061] An "N-sulfonamido" group refers to a "RS0 ₂ N(R _A )-" group in which R and RA can be independently hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl, heteroaryl, heteroalicyclyl, aralkyl, (heteroaryl)alkyl or (heteroalicyclyl)alkyl. An N-sulfonamido may be substituted or unsubstituted.

[0062] An "O-carbamyl" group refers to a "-OC(=0)N(R _{A B} )" group in which R _A and RB can be independently hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl, heteroaryl, heteroalicyclyl, aralkyl, (heteroaryl)alkyl or (heteroalicyclyl)alkyl. An O-carbamyl may be substituted or unsubstituted.

[0063] An "N-carbamyl" group refers to an "ROC(=0)N(R _A )-" group in which R and RA can be independently hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl, heteroaryl, heteroalicyclyl, aralkyl, (heteroaryl)alkyl or (heteroalicyclyl)alkyl. An N-carbamyl may be substituted or unsubstituted.

[0064] An "O-thiocarbamyl" group refers to a "-OC(=S)-N(R _A R _B )" group in which RA and RB can be independently hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl, heteroaryl, heteroalicyclyl, aralkyl, (heteroaryl)alkyl or (heteroalicyclyl)alkyl. An O-thiocarbamyl may be substituted or unsubstituted.

[0065] An "N-thiocarbamyl" group refers to an "ROC(=S)N(R _A )-" group in which R and RA can be independently hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl, heteroaryl, heteroalicyclyl, aralkyl, (heteroaryl)alkyl or (heteroalicyclyl)alkyl. An N-thiocarbamyl may be substituted or unsubstituted.

[0066] A "C-amido" group refers to a "-C(=0)N(R _A R _B )" group in which R _A and R _B can be independently hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl, heteroaryl, heteroalicyclyl, aralkyl, (heteroaryl)alkyl or (heteroalicyclyl)alkyl. A C-amido may be substituted or unsubstituted.

[0067] An "N-amido" group refers to a "RC(=0)N(R _A )-" group in which R and R _A can be independently hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl, heteroaryl, heteroalicyclyl, aralkyl, (heteroaryl)alkyl or (heteroalicyclyl)alkyl. An N-amido may be substituted or unsubstituted.

[0068] The term "halogen atom" or "halogen" as used herein, means any one of the radio-stable atoms of column 7 of the Periodic Table of the Elements, such as, fluorine, chlorine, bromine and iodine.

[0069] Where the numbers of substituents is not specified (e.g. haloalkyl), there may be one or more substituents present. For example "haloalkyl" may include one or more of the same or different halogens. As another example, "C1-C3 alkoxyphenyl" may include one or more of the same or different alkoxy groups containing one, two or three atoms. [0070] As used herein, the abbreviations for any protective groups, amino acids and other compounds, are, unless indicated otherwise, in accord with their common usage, recognized abbreviations, or the IUPAC-IUB Commission on Biochemical Nomenclature (See, Biochem. 1 1 :942-944 (1972)).

[0071] The term "nucleoside" is used herein in its ordinary sense as understood by those skilled in the art, and refers to a compound composed of an optionally substituted pentose moiety or modified pentose moiety attached to a heterocyclic base or tautomer thereof via a N- glycosidic bond, such as attached via the 9-position of a purine-base or the 1 -position of a pyrimidine-base. Examples include, but are not limited to, a ribonucleoside comprising a ribose moiety and a deoxyribonucleoside comprising a deoxyribose moiety. A modified pentose moiety is a pentose moiety in which an oxygen atom has been replaced with a carbon and/or a carbon has been replaced with a sulfur or an oxygen atom. A "nucleoside" is a monomer that can have a substituted base and/or sugar moiety. Additionally, a nucleoside can be incorporated into larger DNA and/or RNA polymers and oligomers. In some instances, the nucleoside can be a nucleoside analog drug.

[0072] The term "nucleotide" is used herein in its ordinary sense as understood by those skilled in the art, and refers to a nucleoside having a phosphate ester bound to the pentose moiety, for example, at the 5 '-position.

[0073] As used herein, the term "heterocyclic base" refers to an optionally substituted nitrogen-containing heterocyclyl that can be attached to an optionally substituted pentose moiety or modified pentose moiety. In some embodiments, the heterocyclic base can be selected from an optionally substituted purine-base, an optionally substituted pyrimidine-base and an optionally substituted triazole-base (for example, a 1,2,4-triazole). The term "purine- base" is used herein in its ordinary sense as understood by those skilled in the art, and includes its tautomers. Similarly, the term "pyrimidine-base" is used herein in its ordinary sense as understood by those skilled in the art, and includes its tautomers. A non-limiting list of optionally substituted purine-bases includes purine, adenine, guanine, hypoxanthine, xanthine, alloxanthine, 7-alkylguanine (e.g. 7-methylguanine), theobromine, caffeine, uric acid and isoguanine. Examples of pyrimidine-bases include, but are not limited to, cytosine, thymine, uracil, 5,6-dihydrouracil and 5-alkylcytosine (e.g., 5-methylcytosine). An example of an optionally substituted triazole-base is l,2,4-triazole-3-carboxamide. Other non-limiting examples of heterocyclic bases include diaminopurine, 8-oxo-N ⁶ -alkyladenine (e.g., 8-oxo-N ⁶ - methyladenine), 7-deazaxanthine, 7-deazaguanine, 7-deazaadenine, N ⁴ ,N ⁴ -ethanocytosin, N ⁶ ,N ⁶ - ethano-2,6-diaminopurine, 5-halouracil (e.g., 5-fluorouracil and 5-bromouracil), pseudoisocytosine, isocytosine, isoguanine, and other heterocyclic bases described in U.S. Patent Nos. 5,432,272 and 7, 125,855, which are incorporated herein by reference for the limited purpose of disclosing additional heterocyclic bases. In some embodiments, a heterocyclic base can be optionally substituted with an amine or an enol protecting group(s).

[0074] The term "-N-linked amino acid" refers to an amino acid that is attached to the indicated moiety via a main-chain amino or mono-substituted amino group. When the amino acid is attached in an -N-linked amino acid, one of the hydrogens that is part of the main-chain amino or mono-substituted amino group is not present and the amino acid is attached via the nitrogen. N-linked amino acids can be substituted or unsubstituted.

[0075] The term "-N-linked amino acid ester derivative" refers to an amino acid in which a main-chain carboxylic acid group has been converted to an ester group. In some embodiments, the ester group has a formula selected from alkyl-0-C(=0)-, cycloalkyl-0-C(=0)- , aryl-0-C(=0)- and aryl(alkyl)-0-C(=0)-. A non-limiting list of ester groups include substituted and unsubstituted versions of the following: methyl-0-C(=0)-, ethyl-0-C(=0)-, n- propyl-0-C(=0)-, isopropyl-0-C(=0)-, n-butyl-0-C(=0)-, isobutyl-0-C(=0)-, tert-butyl-O- C(=0)-, neopentyl-0-C(=0)-, cyclopropyl-0-C(=0)-, cyclobutyl-0-C(=0)-, cyclopentyl-O- C(=0)-, cyclohexyl-0-C(=0)-, phenyl-0-C(=0)-, benzyl-0-C(=0)- and naphthyl-0-C(=0)-. N-linked amino acid ester derivatives can be substituted or unsubstituted.

[0076] The term "-O-linked amino acid" refers to an amino acid that is attached to the indicated moiety via the hydroxy from its main-chain carboxylic acid group. When the amino acid is attached in an -O-linked amino acid, the hydrogen that is part of the hydroxy from its main-chain carboxylic acid group is not present and the amino acid is attached via the oxygen. O-linked amino acids can be substituted or unsubstituted.

[0077] As used herein, the term "amino acid" refers to any amino acid (both standard and non-standard amino acids), including, but not limited to, a-amino acids, β-amino acids, γ- amino acids and δ-amino acids. Examples of suitable amino acids include, but are not limited to, alanine, asparagine, aspartate, cysteine, glutamate, glutamine, glycine, proline, serine, tyrosine, arginine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, threonine, tryptophan and valine. Additional examples of suitable amino acids include, but are not limited to, ornithine, hypusine, 2-aminoisobutyric acid, dehydroalanine, gamma-aminobutyric acid, citrulline, beta-alanine, alpha-ethyl-glycine, alpha-propyl-glycine and norleucine. [0078] The terms "phosphorothioate" and "phosphothioate" refer to a compound of

[0079] As used herein, the term "phosphate" is used in its ordinary sense as understood by those skilled in the art, and includes its protonated forms (for example, As used herein, the terms "monophosphate," "diphosphate," and "triphosphate" are used in their ordinary sense as understood by those skilled in the art, and include protonated forms.

[0080] The terms "protecting group" and "protecting groups" as used herein refer to any atom or group of atoms that is added to a molecule in order to prevent existing groups in the molecule from undergoing unwanted chemical reactions. Examples of protecting group moieties are described in T. W. Greene and P. G. M. Wuts, Protective Groups in Organic Synthesis, 3. Ed. John Wiley & Sons, 1999, and in J.F.W. McOmie, Protective Groups in Organic Chemistry Plenum Press, 1973, both of which are hereby incorporated by reference for the limited purpose of disclosing suitable protecting groups. The protecting group moiety may be chosen in such a way, that they are stable to certain reaction conditions and readily removed at a convenient stage using methodology known from the art. A non-limiting list of protecting groups include benzyl; substituted benzyl; alkylcarbonyls and alkoxycarbonyls (e.g., t-butoxycarbonyl (BOC), acetyl, or isobutyryl); arylalkylcarbonyls and arylalkoxycarbonyls (e.g., benzyloxycarbonyl); substituted methyl ether (e.g. methoxymethyl ether); substituted ethyl ether; a substituted benzyl ether; tetrahydropyranyl ether; silyls (e.g., trimethylsilyl, triethylsilyl, triisopropylsilyl, t- butyldimethylsilyl, tri-z ^' so-propylsilyloxymethyl, [2-(trimethylsilyl)ethoxy]methyl or t- butyldiphenylsilyl); esters (e.g. benzoate ester); carbonates (e.g. methoxymethylcarbonate); sulfonates (e.g. tosylate or mesylate); acyclic ketal (e.g. dimethyl acetal); cyclic ketals (e.g., 1,3- dioxane, 1,3-dioxolanes, and those described herein); acyclic acetal; cyclic acetal (e.g., those described herein); acyclic hemiacetal; cyclic hemiacetal; cyclic dithioketals (e.g., 1,3-dithiane or 1,3-dithiolane); orthoesters (e.g., those described herein) and triarylmethyl groups (e.g., trityl; monomethoxytrityl (MMTr); 4,4'-dimethoxytrityl (DMTr); 4,4',4"-trimethoxytrityl (TMTr); and those described herein). [0081] The term "pharmaceutically acceptable salt" refers to a salt of a compound that does not cause significant irritation to an organism to which it is administered and does not abrogate the biological activity and properties of the compound. In some embodiments, the salt is an acid addition salt of the compound. Pharmaceutical salts can be obtained by reacting a compound with inorganic acids such as hydrohalic acid (e.g., hydrochloric acid or hydrobromic acid), sulfuric acid, nitric acid and phosphoric acid. Pharmaceutical salts can also be obtained by reacting a compound with an organic acid such as aliphatic or aromatic carboxylic or sulfonic acids, for example formic, acetic, succinic, lactic, malic, tartaric, citric, ascorbic, nicotinic, methanesulfonic, ethanesulfonic, p-toluenesulfonic, salicylic or naphthalenesulfonic acid. Pharmaceutical salts can also be obtained by reacting a compound with a base to form a salt such as an ammonium salt, an alkali metal salt, such as a sodium or a potassium salt, an alkaline earth metal salt, such as a calcium or a magnesium salt, a salt of organic bases such as dicyclohexylamine, N-methyl-D-glucamine, tris(hydroxymethyl)methylamine, C1-C7 alkylamine, cyclohexylamine, triethanolamine, ethylenediamine, and salts with amino acids such as arginine and lysine.

[0082] Terms and phrases used in this application, and variations thereof, especially in the appended claims, unless otherwise expressly stated, should be construed as open ended as opposed to limiting. As examples of the foregoing, the term 'including' should be read to mean 'including, without limitation,' 'including but not limited to,' or the like; the term 'comprising' as used herein is synonymous with 'including,' 'containing,' or 'characterized by,' and is inclusive or open-ended and does not exclude additional, unrecited elements or method steps; the term 'having' should be interpreted as 'having at least;' the term 'includes' should be interpreted as 'includes but is not limited to;' the term 'example' is used to provide exemplary instances of the item in discussion, not an exhaustive or limiting list thereof; and use of terms like 'preferably,' 'preferred,' 'desired,' or 'desirable,' and words of similar meaning should not be understood as implying that certain features are critical, essential, or even important to the structure or function, but instead as merely intended to highlight alternative or additional features that may or may not be utilized in a particular embodiment. In addition, the term "comprising" is to be interpreted synonymously with the phrases "having at least" or "including at least". When used in the context of a process, the term "comprising" means that the process includes at least the recited steps, but may include additional steps. When used in the context of a compound, composition or device, the term "comprising" means that the compound, composition or device includes at least the recited features or components, but may also include additional features or components. Likewise, a group of items linked with the conjunction 'and' should not be read as requiring that each and every one of those items be present in the grouping, but rather should be read as 'and/or' unless expressly stated otherwise. Similarly, a group of items linked with the conjunction Or' should not be read as requiring mutual exclusivity among that group, but rather should be read as 'and/or' unless expressly stated otherwise.

[0083] With respect to the use of substantially any plural and/or singular terms herein, those having skill in the art can translate from the plural to the singular and/or from the singular to the plural as is appropriate to the context and/or application. The various singular/plural permutations may be expressly set forth herein for sake of clarity. The indefinite article "a" or "an" does not exclude a plurality. A single processor or other unit may fulfill the functions of several items recited in the claims. The mere fact that certain measures are recited in mutually different dependent claims does not indicate that a combination of these measures cannot be used to advantage. Any reference signs in the claims should not be construed as limiting the scope.

[0084] It is understood that, in any compound described herein having one or more chiral centers, if an absolute stereochemistry is not expressly indicated, then each center may independently be of R-configuration or S-configuration or a mixture thereof. Thus, the compounds provided herein may be enantiomerically pure, enantiomerically enriched, racemic mixture, diastereomerically pure, diastereomerically enriched, or a stereoisomeric mixture. In addition it is understood that, in any compound described herein having one or more double bond(s) generating geometrical isomers that can be defined as E or Z, each double bond may independently be E or Z a mixture thereof.

[0085] Likewise, it is understood that, in any compound described, all tautomeric forms are also intended to be included. For example all tautomers of a phosphate and a phosphorothioate groups are intended to be included. Examples of tautomers of a

phosphorothioate include the following: and . Furthermore, all tautomers of heterocyclic bases known in the art are intended to be included, including tautomers of natural and non-natural purine-bases and pyrimidine- bases. [0086] It is to be understood that where compounds disclosed herein have unfilled valencies, then the valencies are to be filled with hydrogens or isotopes thereof, e.g., hydrogen- 1 (protium) and hydrogen-2 (deuterium).

[0087] It is understood that the compounds described herein can be labeled isotopically. Substitution with isotopes such as deuterium may afford certain therapeutic advantages resulting from greater metabolic stability, such as, for example, increased in vivo half-life or reduced dosage requirements. Each chemical element as represented in a compound structure may include any isotope of said element. For example, in a compound structure a hydrogen atom may be explicitly disclosed or understood to be present in the compound. At any position of the compound that a hydrogen atom may be present, the hydrogen atom can be any isotope of hydrogen, including but not limited to hydrogen- 1 (protium) and hydrogen-2 (deuterium). Thus, reference herein to a compound encompasses all potential isotopic forms unless the context clearly dictates otherwise.

[0088] It is understood that the methods and combinations described herein include crystalline forms (also known as polymorphs, which include the different crystal packing arrangements of the same elemental composition of a compound), amorphous phases, salts, solvates and hydrates. In some embodiments, the compounds described herein exist in solvated forms with pharmaceutically acceptable solvents such as water, ethanol, or the like. In other embodiments, the compounds described herein exist in unsolvated form. Solvates contain either stoichiometric or non-stoichiometric amounts of a solvent, and may be formed during the process of crystallization with pharmaceutically acceptable solvents such as water, ethanol, or the like. Hydrates are formed when the solvent is water, or alcoholates are formed when the solvent is alcohol. In addition, the compounds provided herein can exist in unsolvated as well as solvated forms. In general, the solvated forms are considered equivalent to the unsolvated forms for the purposes of the compounds and methods provided herein.

[0089] Where a range of values is provided, it is understood that the upper and lower limit, and each intervening value between the upper and lower limit of the range is encompassed within the embodiments. Compounds

[0090] Some embodiments disclosed herein relate to a compound of Formula (I) or a pharmaceutically acceptable salt thereof:

from an unsubstituted Ci_6 alkyl, an unsubstituted C2-6 alkenyl, an unsubstituted C2-6 alkynyl, an unsubstituted C ₃ -6 cycloalkyl and an unsubstituted Ci_6 haloalkyl; R ² can be halo, -OR ^9A or -

N(R ^9B R ^9C ); R ³ can be hydrogen or R ^4A ; R ^4A can be selected from 0-, OH, an optionally substituted N-linked amino acid and an optionally substituted N-linked amino acid ester derivative; R ^4B can be selected from O ^" , OH, an -O-optionally substituted aryl, an -O- optionally substituted heteroaryl, an -O-optionally substituted heterocyclyl, an optionally substituted N-linked amino acid, an optionally substituted N-linked amino acid ester derivative

R ⁵ and R ⁶ can be independently selected from hydrogen, an unsubstituted Ci_6 alkyl, an unsubstituted C ₃ -6 alkenyl, an unsubstituted C ₃ -6 alkynyl and an unsubstituted C ₃ -6 cycloalkyl; R ⁷ can be NHR ¹³ ; R ⁸ can be NHR ¹⁴ ; R ^9A can be hydrogen or - C(=0)R ¹⁵ ; R ^9B and R ^9C can be independently hydrogen or an optionally substituted Ci_6 alkyl; R ¹⁰ , R ¹¹ and R ¹² can be independently absent or hydrogen; R ¹³ can be selected from hydrogen, an optionally substituted Ci_6 alkyl, an optionally substituted C3-6 alkenyl, an optionally substituted C ₃ - ₆ cycloalkyl, -C(=0)R ^A1 and -C(=0)OR ^A2 ; R ¹⁴ can be selected from hydrogen, an optionally substituted Ci_6 alkyl, an optionally substituted C3-6 alkenyl, an optionally substituted C3-6 cycloalkyl, -C(=0)R ^A3 and -C(=0)OR ^A4 ; R ¹⁵ can be an optionally substituted Ci_ ₆ alkyl or an optionally substituted C3-6 cycloalkyl; X can be N or -CR ¹⁶ ; R ¹⁶ can be selected from hydrogen, halogen, an optionally substituted Ci_6 alkyl, an optionally substituted C2-6 alkenyl and an optionally substituted C2-6 alkynyl; R ^A1 , R ^A2 , R ^A3 and R ^A4 can be independently selected from Ci-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, C3-6 cycloalkyl, C3-6 cycloalkenyl, C6-10 aryl, heteroaryl, heteroalicyclyl, aryl(Ci_6 alkyl), heteroaryl(Ci_6 alkyl) and heteroalicyclyl(Ci_6 alkyl); n can be 0

and R ^4A is O ^" or OH, then R ^4B

[0091] The substituents attached to the 2'-carbon can vary. In some embodiments, R ² can be halo. For example, R ² can be fluoro or chloro. In other embodiments, R ² can be -OH. In still other embodiments, R ² can be OR ^9A , wherein R ^9A can be -C(=0)R ¹⁵ , and R ¹⁵ can be an optionally substituted Ci_6 alkyl. Suitable alkyl groups include, but are not limited to optionally substituted variants of the following: methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert- butyl, pentyl (branched and straight-chained) and hexyl (branched and straight-chained). In yet still other embodiments, R ² can be OR ^9A , wherein R ^9A can be -C(=0)R ¹⁵ , and R ¹⁵ can be an optionally substituted C3-6 cycloalkyl. Suitable cycloalkyl groups include, but are not limited to optionally substituted variants of the following: cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl. In some embodiment, R ² can be -N(R ^9B R ^9C ), wherein R ^9B and R ^9C can be independently hydrogen or an optionally substituted Ci_6 alkyl. In some embodiments, R ^9B and

_R 9C

can be both hydrogen. In other embodiments, at least one of R ^9B and R ^9C can be an optionally substituted Ci_6 alkyl. In some embodiments, R ^9B and R ^9C can be both an optionally substituted Ci_6 alkyl. In some embodiments, R ^9B and R ^9C can be the same. In other embodiments, R ^9B and R ^9C can be different.

[0092] In some embodiments, R ¹ can be an unsubstituted Ci_6 alkyl. For example, R ¹ can be unsubstituted methyl, unsubstituted ethyl, unsubstituted n-propyl, unsubstituted isopropyl, unsubstituted n-butyl, unsubstituted isobutyl, unsubstituted tert-butyl, unsubstituted pentyl (branched and straight-chained) or unsubstituted hexyl (branched and straight-chained). In some embodiments, R ¹ can be an unsubstituted C2-6 alkenyl. For example, R ¹ can be ethenyl, n-propenyl, isopropenyl, n-butenyl, isobutenyl, tert-butenyl, pentenyl (branched and straight- chained), hexenyl (branched and straight-chained), vinyl or allenyl. In some embodiments, R ¹ can be an unsubstituted alkynyl. Suitable alkynyl groups include, but are not limited to the following: ethenyl, propynyl, n-butynyl, isobutynyl-, tert-butynyl, pentynyl (branched and straight-chained) and hexynyl (branched and straight-chained). In still other embodiments, R ¹ can be an unsubstituted C3-6 cycloalkyl such as those described herein. In yet other embodiments, R ¹ can be an unsubstituted haloalkyl. Examples of suitable haloalkyl include, but are not limited to, chloromethyl, fluoromethyl, difluoromethyl, trifluoromethyl, l-chloro-2- fluoromethyl and 2-fluoroisobutyl.

3] In some embodiments, R ³ can be hydrogen. In other embodiments, R ³ can be . In some embodiments, the compound of Formula (I) can be a monophosphate. In other embodiments, the compound of Formula (I) can be a thiomonophosphate. In some embodiments, the compound of Formula (I) can be a diphosphate. In other embodiments, the compound of Formula (I) can be an alpha-thiodiphosphate. In some embodiments, the compound of Formula (I) can be a triphosphate. In other embodiments, the compound of Formula (I) can be an alpha-thiotriphosphate. In some embodiments, R ^4A can be O ^" or OH; and R ^4B can be O ^" or OH. In other embodiments, R ^4A can be O ^" or OH; and R ^4B can be

, wherein R ¹⁰ , R ¹¹ and R ¹² can be independently absent or hydrogen; and n can be 0. In still other embodiments, R ^4A can be O ^" or OH; and R ^4B can be

, wherein R ¹⁰ , R ¹¹ and R ¹² can be independently absent or hydrogen; and n can be 1. The substituents attached to the phosphorus can vary. In some embodiments, a compound of Formula (I) can be a phosphoramidate. In other embodiments, a compound of Formula (I) can be a thiophosphoramidate. In still other embodiments, a compound of Formula (I) can be a phosphorbisamidate. In yet still other embodiments, a compound of Formula (I) can be a thiophosphorbisamidate. [0094] In some embodiments, R can be an optionally substituted N-linked amino acid. Various amino acids are suitable, including those described herein. Examples of suitable amino acids include, but are not limited to, alanine, asparagine, aspartate, cysteine, glutamate, glutamine, glycine, proline, serine, tyrosine, arginine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, threonine, tryptophan and valine. In other embodiments, R ^4A can be an optionally substituted N-linked amino acid ester derivative. Examples of N-linked amino acid ester derivatives include, but are not limited to, ester derivatives of any of the following amino acids: alanine, asparagine, aspartate, cysteine, glutamate, glutamine, glycine, proline, serine, tyrosine, arginine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, threonine, tryptophan and valine. Additional examples of N-linked amino acid ester derivatives include, but are not limited to, an ester derivative of any of the following amino acids: alpha- ethyl-glycine, alpha-propyl-glycine and beta-alanine. In some embodiments, the N-linked amino acid ester derivative can be a C e alkyl ester derivative, for example, an isopropyl ester of alanine. In other embodiments, the N-linked amino acid ester derivative can be a C3-6 cycloalkyl ester derivative, such as a cyclohexyl ester of alanine.

some embodiments, R ^4A can have the structure wherein R can be selected from hydrogen, an optionally substituted Ci_6- alkyl, an optionally substituted C3-6 cycloalkyl, an optionally substituted aryl, an optionally substituted aryl(Ci-6 alkyl) and an optionally substituted haloalkyl; R ¹⁸ can be selected from hydrogen, an optionally substituted C e alkyl, an optionally substituted C e haloalkyl, an optionally substituted C3-6 cycloalkyl, an optionally substituted Ce aryl, an optionally substituted Cio aryl and an optionally substituted aryl(Ci-6 alkyl); and R ¹⁹ can be hydrogen or an optionally substituted Ci-4-alkyl.

[0096] When R ¹⁸ is substituted, R ¹⁸ can be substituted with one or more substituents selected from N-amido, mercapto, alkylthio, an optionally substituted aryl, hydroxy, an optionally substituted heteroaryl, O-carboxy and amino. In some embodiments, R ¹⁸ can be hydrogen. In some embodiments, R ¹⁸ can be an unsubstituted Ci_6-alkyl, such as those described herein. In other embodiments, R ¹⁸ can be methyl. In some embodiments, R ¹⁷ can be an optionally substituted Ci_6 alkyl. Examples of optionally substituted Ci-6-alkyls include optionally substituted variants of the following: methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, pentyl (branched and straight-chained) and hexyl (branched and straight- chained). In some embodiments, R ¹⁷ can be methyl or isopropyl. In some embodiments, R ¹⁷ can be ethyl or neopentyl. In other embodiments, R can be an optionally substituted C3-6 cycloalkyl. Examples of optionally substituted C3-6 cycloalkyl include optionally substituted variants of the following: cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl. In some embodiments, R ¹⁷ can be an optionally substituted cyclohexyl. In still other embodiments, R ¹⁷ can be an optionally substituted aryl, such as phenyl and naphthyl. In yet still other embodiments, R ¹⁷ can be an optionally substituted aryl(Ci_6 alkyl). In some embodiments, R ¹⁷ can be an optionally substituted benzyl. In some embodiments, R ¹⁷ can be an optionally substituted C e haloalkyl, for example, CF ₃ . In some embodiments, R ¹⁹ can be hydrogen. In other embodiments, R ¹⁹ can be an optionally substituted Ci-4-alkyl, such as methyl, ethyl, n- propyl, isopropyl, n-butyl, isobutyl or tert-butyl. In some embodiments, R ¹⁹ can be methyl. Depending on the groups that are selected for R ¹⁸ and R ¹⁹ , the carbon to which R ¹⁸ and R ¹⁹ are attached may be a chiral center. In some embodiment, the carbon to which R ¹⁸ and R ¹⁹ are attached may be a (R)-chiral center. In other embodiments, the carbon to which R ¹⁸ and R ¹⁹ are attached may be a (S)-chiral center.

[0097] Examples of suitable groups include the following:

[0098] In some embodiments, R ^4B can be an -O-optionally substituted aryl. For example, R ^4B can be an -O-optionally substituted phenyl. When the phenyl is substituted, the ring can be substituted 1, 2, 3 or more than 3 times. Suitable mono-substituted phenyl groups include, ortho-substituted phenyl, meta-substituted phenyl and para-substituted phenyl. In some embodiments, R ^4B can be ortho-chlorophenyl. In some embodiments, R ^4B can be 3-chloro-4- fluorophenyl. Alternatively, R ^4B can be an -O-optionally substituted naphthyl. In other embodiments, R ^4B can be an -O-optionally substituted heteroaryl. In still other embodiments, R ^4B can be an -O-optionally substituted heterocyclyl.

[0099] In some embodiments, R ^4B can be an optionally substituted N-linked amino acid, such as those described for R ^4A . In other embodiments, R ^4B can be an optionally substituted N-linked amino acid ester derivative, for example, those described herein. In some , 20

embodiments, R can have the structure wherein R ^zu can be selected from hydrogen, an optionally substituted Ci-6-alkyl, an optionally substituted C3-6 cycloalkyl, an optionally substituted aryl, an optionally substituted aryl(Ci_6 alkyl) and an optionally substituted haloalkyl; R ²¹ can be selected from hydrogen, an optionally substituted Ci_6 alkyl, an optionally substituted Ci_6 haloalkyl, an optionally substituted C3-6 cycloalkyl, an optionally substituted Ce aryl, an optionally substituted C1 ₀ aryl and an optionally substituted aryl(Ci_6 alkyl); and R ²² can be hydrogen or an optionally substituted Ci-4-alkyl.

[0100] When R ²¹ is substituted, R ²¹ can be substituted with one or more substituents selected from N-amido, mercapto, alkylthio, an optionally substituted aryl, hydroxy, an optionally substituted heteroaryl, O-carboxy and amino. In some embodiments, R ²¹ can be an unsubstituted Ci_6-alkyl, such as those described herein. In some embodiments, R ²¹ can be hydrogen. In other embodiments, R ²¹ can be methyl. In some embodiments, R ²⁰ can be an optionally substituted Ci_6 alkyl. Examples of optionally substituted Ci_6 alkyls include optionally substituted variants of the following: methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, pentyl (branched and straight-chained) and hexyl (branched and straight- chained). In some embodiments, R ²⁰ can be methyl or isopropyl. In some embodiments, R ²⁰ can be ethyl or neopentyl. In other embodiments, R ²⁰ can be an optionally substituted C3-6 cycloalkyl. Examples of optionally substituted C3-6 cycloalkyl include optionally substituted variants of the following: cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl. In an embodiment, R ²⁰ can be an optionally substituted cyclohexyl. In still other embodiments, R ²⁰ can be an optionally substituted aryl, such as phenyl and naphthyl. In yet still other embodiments, R ²⁰ can be an optionally substituted aryl(Ci_6 alkyl). In some embodiments, R ²⁰ can be an optionally substituted benzyl. In some embodiments, R ²⁰ can be an optionally substituted Ci_6 haloalkyl, for example, CF ₃ . In some embodiments, R ²² can be hydrogen. In other embodiments, R ²² can be an optionally substituted Ci-4-alkyl, such as methyl, ethyl, n- propyl, isopropyl, n-butyl, isobutyl or tert-butyl. In an embodiment, R ²² can be methyl.

21 22 21 22

Depending on the groups that are selected for R and R , the carbon to which R and R are attached may be a chiral center. In some embodiment, the carbon to which R ²¹ and R ²² are attached may be a (R)-chiral center. In other embodiments, the carbon to which R ²¹ and R ²² are attached may be a (S)-chiral center. :

[0102] In some embodiments, R ^4A can be an optionally substituted N-linked amino acid or an optionally substituted N-linked amino acid ester derivative and R ^4B can be an -O- optionally substituted aryl. In other embodiments, R ^4A can be an optionally substituted N-linked amino acid or an optionally substituted N-linked amino acid ester derivative and R ^4B can be an - O-optionally substituted heteroaryl. In some embodiments, R ^4A can be an optionally substituted N-linked amino acid or an optionally substituted N-linked amino acid ester derivative and R ^4B can be an optionally substituted N-linked amino acid or an optionally substituted N-linked amino acid ester derivative. In some embodiments, R ^4A and R ^4B can be the same. In other embodiments, R ^4A and R ^4B can be different.

[0103] The nucleobase can vary. In some embodiments, B ¹ can be guanine. In some

embodiments, B ¹ can be an optionally substituted In other embodiments, B ¹ can be an optionally substituted wherein R can be selected from hydrogen, an unsubstituted Ci_6 alkyl, an unsubstituted C3-6 alkenyl, unsubstituted C3-6 alkynyl and an unsubstituted C3-6 cycloalkyl. In some embodiments, B ¹

be unsubstituted . In some embodiments, R can be an unsubstituted C e alkyl. For example, R ⁵ can be methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, pentyl (branched and straight-chained) or hexyl (branched and straight-chained). In some embodiments, R ⁵ can be an unsubstituted C3-6 alkenyl. In other embodiments, R ⁵ can be an unsubstituted C3-6 alkynyl. In still other embodiments, R ⁵ can be an unsubstituted C3-6 cycloalkyl, for example, cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl.

[0104] In some embodiments, B ¹ can be an optionally substituted

wherein R ⁶ can be selected from hydrogen, an unsubstituted Ci_6 alkyl, an unsubstituted C3-6 alkenyl, an unsubstituted C3-6 alkynyl and an unsubstituted C3-6 cycloalkyl.

In some embodiments, B ¹ can be unsubstituted In some embodiments,

R can be hydrogen. In some embodiments, R can be an unsubstituted Ci_6 alkyl. For example, R ⁶ can be methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, pentyl (branched and straight-chained) or hexyl (branched and straight-chained). In some embodiments, R ⁶ can be an ethyl. In some embodiments, R ⁶ can be an unsubstituted C3-6 alkenyl. In other embodiments, R ⁶ can be an unsubstituted C3-6 alkynyl. In other embodiments, R ⁶ can be an unsubstituted C3-6 cycloalkyl, for example, cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl.

some embodiments, B ¹ can be an optionally substituted

wherein X can be N or -CR ¹⁶ ; R ¹⁶ can be selected from hydi halogen, an optionally substituted Ci_6 alkyl, an optionally substituted C2-6 alkenyl and an

7 13 8 14 13

optionally substituted C2-6 alkynyl; R can be NHR , R° can be NHR , R ^1J can be selected from hydrogen, an optionally substituted Ci_6 alkyl, an optionally substituted C3-6 alkenyl, an optionally substituted C ₃ - ₆ cycloalkyl, -C(=0)R ^A1 and -C(=0)OR ^A2 ; R ¹⁴ can be selected from hydrogen, an optionally substituted Ci_6 alkyl, an optionally substituted C3-6 alkenyl, an optionally substituted C ₃ - ₆ cycloalkyl, -C(=0)R ^A3 and -C(=0)OR ^A4 _; R ^A1 , R ^A2 , R ^A3 and R ^A4 can be independently selected from Ci_6 alkyl, C2-6 alkenyl, C2-6 alkynyl, C3-6 cycloalkyl, C3-6 cycloalkenyl, C6-10 aryl, heteroaryl, heteroalicyclyl, aryl(Ci_6 alkyl), heteroaryl(Ci_6 alkyl) and heteroalicyclyl(Ci_6 alkyl). In other embodiments, B ¹ can be an unsubstituted

In some embodiments, X can be N (nitrogen). In other embodiments,

X ¹ can be -CR ¹⁶ , wherein R ¹⁶ can be selected from hydrogen, halogen, an optionally substituted Ci-6 alkyl, an optionally substituted C2-6 alkenyl and an optionally substituted C2-6 alkynyl. In some embodiments, X ¹ can be CH. In some embodiments, R ⁷ and R ⁸ can be both N¾. In other embodiments, at least one of R ⁷ and R ⁸ can be N¾. In some embodiments, R ⁷ can be NHR ¹³ , wherein R ¹³ can be an optionally substituted Ci_6 alkyl. In some embodiments, R ⁸ can be NHR ¹⁴ , wherein R ¹⁴ can be an optionally substituted Ci_6 alkyl. In other embodiments, R ⁷ can be NHR ¹³ , wherein R ¹³ can be selected from an optionally substituted C ₃ -6 alkenyl, an optionally substituted C ₃ - ₆ cycloalkyl, -C(=0)R ^A1 and -C(=0)OR ^A2 . In other embodiments, R ⁸ can be NHR ¹⁴ , wherein R ¹⁴ can be selected from an optionally substituted C ₃ -6 alkenyl, an optionally substituted C3-6 cycloalkyl, -C(=0)R ^A3 and -C(=0)OR ^A4 . In some embodiments, R ⁷ and R ⁸ can be the same. In other embodiments, R ⁷ and R ⁸ can be different. In some embodiments, B ¹ can

[0106] In some embodiments, Z ¹ can be O (oxygen). In other embodiments, Z ¹ can be S (sulfur).

[0107] Some examples of compounds of Formula (I) include, but are not limited to the following:

the foregoing.

[0108] Further examples of compounds of Formula (I) include, but are not limited to the following:

or a pharmaceutically acceptable salt of the foregoing.

[0109] As described herein, a compound of Formula (I), or a pharmaceutically

acceptable salt thereof, can have R ³ being R being an optionally substituted N- linked amino acid or an optionally substituted N-linked amino acid ester derivative; and R being an -O-optionally substituted aryl, an -O-optionally substituted heteroaryl, an -O- optionally substituted heterocyclyl, an optionally substituted N-linked amino acid or an optionally substituted N-linked amino acid ester derivative . By neutralizing the charge on the phosphate or thiophosphate, penetration of the cell membrane may be facilitated as a result of the increased lipophilicity of the compound. Once absorbed and taken inside the cell, the groups attached to the phosphorus can be easily removed by esterases, proteases and/or other enzymes. In some embodiments, the groups attached to the phosphorus can be removed by simple hydrolysis. Inside the cell, the phosphate thus released may then be metabolized by cellular enzymes to the diphosphate or the active triphosphate. Likewise, the thio-phosphate may be metabolized to the alpha-thiodiphosphate or the alpha-thiotriphosphate. Furthermore, in some embodiments, varying the substituents on a compound described herein, such as compound of Formula (I), can help maintain the efficacy of such the compound by reducing undesirable effects, such as isomerization.

[0110] In some embodiments, the phosphorylation of a thio-monophosphate of a compound of Formula (I), or pharmaceutically acceptable salt thereof, can be stereoselective. For example, a thio-monophosphate of a compound of Formula (I) can be phosphorylated to give an alpha-thiodiphosphate and/or an alpha-thiotriphosphate compound that can be enriched in the (R) or (S) diastereomer with respect to the 5 '-0-phosphorous atom. For example, one of the (R) and (S) configuration with respect to the 5 '-0-phosphorous atom of the alpha- thiodiphosphate and/or the alpha-thiotriphosphate compound can be present in an amount > 50%, > 75%, > 90%, > 95% or > 99% compared to the amount of the other of the (R) or (S) configuration with respect to the 5'-0-phosphorous atom. In some embodiments, phosphorylation of a compound of Formula (I), or pharmaceutically acceptable salt thereof, can result in the formation of a compound that has the (R)-configuration at the 5'-0-phosphorous atom. In some embodiments, phosphorylation of a compound of Formula (I), or pharmaceutically acceptable salt thereof, can result in formation of a compound that has the (5)- configuration at the 5'-0-phosphorous atom.

[0111] In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can act as a chain terminator of HCV replication. For example, since compounds of Formula (I) do not contain a hydroxyl group at the 3 '-position, once the compound is incorporated into an RNA chain no further chain elongation can occur.

[0112] In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can have increased metabolic and/or plasma stability. In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can be more resistant to hydrolysis and/or more resistant to enzymatic transformations. For example, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can have increased metabolic stability, increased plasma stability, can be more resistant to hydrolysis and/or can be more resistant to enzymatic transformations compared to a compound that is identical in structure but for having a OH group in place of the fluoro at the 3 '-position. In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can have improved properties. A non-limiting list of example properties include, but are not limited to, increased biological half-life, increased bioavailability, increase potency, a sustained in vivo response, increased dosing intervals, decreased dosing amounts, decreased cytotoxicity, reduction in required amounts for treating disease conditions, reduction in viral load, reduction in time to seroconversion (i.e., the virus becomes undetectable in patient serum), increased sustained viral response, a reduction of morbidity or mortality in clinical outcomes, increased subject compliance, decreased liver conditions (such as liver fibrosis, liver cirrhosis and/or liver cancer), and compatibility with other medications. In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can have a biological half-life of greater than 24 hours. In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can have a biological half-life greater than a compound that is identical in structure but for having a OH group in place of the fluoro at the 3 '-position. In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can have more potent antiviral activity (for example, a lower EC5 ₀ in an HCV replicon assay) as compared to the current standard of care. In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, does not significantly inhibit mitochondrial function of the mitochondrial RNA polymerase. For example, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, is incorporated in the human mitochondrial RNA polymerase less than 10% compared to the natural 5 '-triphosphate nucleotide with the same B ¹ .

[0113] Additionally, in some embodiments, the presence of a thiophosphoramidate, phosphoramidate, thiophosphorbisamidate or phosphorbisamidate in a compound of Formula (I) can increase the stability of the compound by inhibiting its degradation. Also, in some embodiments, the presence of a thiophosphoramidate, phosphoramidate, thiophosphorbisamidate or phosphorbisamidate can make the compound more resistant to cleavage in vivo and provide sustained, extended efficacy. In some embodiments, a thiophosphoramidate, phosphoramidate, thiophosphorbisamidate or phosphorbisamidate can facilitate the penetration of the cell membrane by a compound of Formula (I) by making the compound more lipophilic. In some embodiments, a thiophosphoramidate, phosphoramidate, thiophosphorbisamidate or phosphorbisamidate can have improved oral bioavailability, improved aqueous stability and/or reduced risk of byproduct-related toxicity. In some embodiments, for comparison purposes, a compound of Formula (I) can be compared to a compound that is identical in structure but for having a OH group in place of the fluoro at the 3 '- position.

Synthesis

[0114] Compounds of Formula (I) and those described herein may be prepared in various ways. General synthetic routes to the compound of Formula (I), and some examples of starting materials used to synthesize the compounds of Formula (I) are shown in Schemes 1 and 2, and described herein. The routes shown and described herein are illustrative only and are not intended, nor are they to be construed, to limit the scope of the claims in any manner whatsoever. Those skilled in the art will be able to recognize modifications of the disclosed syntheses and to devise alternate routes based on the disclosures herein; all such modifications and alternate routes are within the scope of the claims.

[0115] Compounds of Formula (I) can be prepared using various methods known to those skilled in the art. Examples of methods are shown in Schemes 1 and 2. Suitable phosphorus containing precursors can be commercially obtained or prepared by synthetic methods known to those skilled in the art. Examples of general structures of phosphorus containing precursors are shown in Schemes 1 and 2, and include phosphorochloridates and thiophosphorochloridates. Suitable phosphorochloridates and thiophosphorochloridates are commercially available and/or can be synthetically prepared. Scheme 1

(A) (B)

[0116] One method for forming a compound of Formula (I) is shown in Scheme 1. In Scheme 1, R ^la , R ^2a and B ^la can be the same as R ¹ , R ² and B ¹ as described herein for Formula (I). In some embodiments, a compound of Formula (I) can be generated from a compound of Formula (A) and a compound of Formula (B) using an organometallic reagent, such as a Grignard reagent. Suitable Grignard reagents are known to those skilled in the art and include, but are not limited to, alkylmagnesium chlorides and alkylmagnesium bromides. In other embodiments, an appropriate base can be used to form a compound of Formula (I). Examples of suitable bases include, but are not limited to, an amine base, such as an alkylamine (including mono-, di- and tri-alkylamines (e.g., triethylamine)), optionally substituted pyridines (e.g. collidine) and optionally substituted imidazoles (e.g., N-methylimidazole)).

[0117] When compounds of Formula (I) has Z ¹ being sulfur, the sulfur can be added in various manners. In some embodiments, the sulfur can be part of the phosphorus containing

precursor, for example, . Alternatively, one of the oxygens attached to the phosphorus can be exchanged with a sulfur using a sulfurization reagent. Suitable sulfurization agents are known to those skilled in the art, and include, but are not limited to, elemental sulfur, Lawesson's reagent, cyclooctasulfur, 3H-l,2-Benzodithiole-3-one-l, l-dioxide (Beaucage's reagent), 3-((N,N-dimethylaminomethylidene)amino)-3H-l,2,4-dithiazole- 5-thione (DDTT) and bis(3-triethoxysilyl)propyl-tetrasulfide (TEST).

Scheme 2

[0118] A phosphorus containing precursor can be coupled to the nucleoside, for example, a compound of Formula (A). Following the coupling of the phosphorus containing precursor, any leaving groups can be cleaved under suitable conditions, such as hydrolysis. In Scheme 2, R ^la , R ^2a and B ^la can be the same as R ¹ , R ² and B ¹ as described herein for Formula (I). Further phosphorus containing groups can be added using methods known to those skilled in the art, for example using a pyrophosphate. If desired, one or more bases can be used during the addition of each phosphorus-containing group. Examples of suitable bases are described herein.

[0119] As provided herein, R ² can be -OC(=0)R ¹⁵ . The -OC(=0)R ¹⁵ group can be formed at the 2 '-position using various methods known to those skilled in the art. As an example, a compound of Formula (I), wherein R ² is a hydroxy group, can be treated with an alkyl anhydride (e.g., acetic anhydride and propionic anhydride) or an alkyl acid chloride (e.g., acetylchloride). If desired, a catalyst can be used to facilitate the reaction. An example of suitable catalyst is 4-dimethylaminopyridine (DMAP). Alternatively, the -OC(=0) ¹⁵ group can be formed at the 2'-position by reacting an alkyl acid (e.g. acetic acid and propionic acid) in the presences of a carbodiimide or a coupling reagent. Examples of carbodiimides include, but are not limited to, Ν,Ν'-dicyclohexylcarbodiimide (DCC), Ν,Ν'-diisopropylcarbodiimide (DIC) and l-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDC).

[0120] To reduce the formation of side products, one or more the groups attached to the pentose ring can be protected with one or more suitable protecting groups. As an example, if R ² is a hydroxy group, the hydroxy group can be protected with a suitable protecting group, such as triarylmethyl and/or silyl group. Examples of triarylmethyl groups include but are not limited to, trityl, monomethoxytrityl (MMTr), 4,4'-dimethoxytrityl (DMTr), 4,4',4"- trimethoxytrityl (TMTr),. 4,4',4"-tris- (benzoyloxy) trityl (TBTr), 4,4',4"-tris (4,5- dichlorophthalimido) trityl (CPTr), 4,4',4"-tris (levulinyloxy) trityl (TLTr), p-anisyl-1- naphthylphenylmethyl, di-o-anisyl-l-naphthylmethyl, p-tolyldipheylmethyl, 3- (imidazolylmethyl)-4,4'-dimethoxytrityl, 9-phenylxanthen-9-yl (Pixyl), 9-(p-methoxyphenyl) xanthen-9-yl (Mox), 4-decyloxytrityl, 4- hexadecyloxytrityl, 4,4'-dioctadecyltrityl, 9-(4- octadecyloxyphenyl) xanthen-9-yl, l,r-bis-(4-methoxyphenyl)-l'-pyrenylmethyl, 4,4',4"-tris- (tert-butylphenyl) methyl (TTTr) and 4,4'-di-3, 5-hexadienoxytrityl. Examples of suitable silyl groups are described herein and include trimethylsilyl (TMS), tert-butyldimethylsilyl (TBDMS), triisopropylsilyl (TIPS), tert-butyldiphenylsilyl (TBDPS), tri-zso-propylsilyloxymethyl and [2- (trimethylsilyl)ethoxy]methyl.

Pharmaceutical Compositions

[0121] Some embodiments described herein relates to a pharmaceutical composition, that can include a therapeutically effective amount of one or more compounds described herein (e.g., a compound of Formula (I)), or a pharmaceutically acceptable salt thereof) and a pharmaceutically acceptable carrier, diluent, excipient or combination thereof. In some embodiments, the pharmaceutical composition can include a single diastereomer of a compound of Formula (I), or a pharmaceutically acceptable salt thereof, (for example, a single diastereomer is present in the pharmaceutical composition at a concentration of greater than 99% compared to the total concentration of the other diastereomers). In other embodiments, the pharmaceutical composition can include a mixture of diastereomers of a compound of Formula (I), or a pharmaceutically acceptable salt thereof. For example, the pharmaceutical composition can include a concentration of one diastereomer of > 50%, > 60%, > 70%, > 80%, > 90%, > 95%, or > 98%, as compared to the total concentration of the other diastereomers. In some embodiments, the pharmaceutical composition includes a 1 : 1 mixture of two diastereomers of a compound of Formula (I), or a pharmaceutically acceptable salt thereof.

[0122] The term "pharmaceutical composition" refers to a mixture of one or more compounds disclosed herein with other chemical components, such as diluents or carriers. The pharmaceutical composition facilitates administration of the compound to an organism. Pharmaceutical compositions can also be obtained by reacting compounds with inorganic or organic acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, methanesulfonic acid, ethanesulfonic acid, p-toluenesulfonic acid and salicylic acid. Pharmaceutical compositions will generally be tailored to the specific intended route of administration. [0123] The term "physiologically acceptable" defines a carrier, diluent or excipient that does not abrogate the biological activity and properties of the compound.

[0124] As used herein, a "carrier" refers to a compound that facilitates the incorporation of a compound into cells or tissues. For example, without limitation, dimethyl sulfoxide (DMSO) is a commonly utilized carrier that facilitates the uptake of many organic compounds into cells or tissues of a subject.

[0125] As used herein, a "diluent" refers to an ingredient in a pharmaceutical composition that lacks pharmacological activity but may be pharmaceutically necessary or desirable. For example, a diluent may be used to increase the bulk of a potent drug whose mass is too small for manufacture and/or administration. It may also be a liquid for the dissolution of a drug to be administered by injection, ingestion or inhalation. A common form of diluent in the art is a buffered aqueous solution such as, without limitation, phosphate buffered saline that mimics the composition of human blood.

[0126] As used herein, an "excipient" refers to an inert substance that is added to a pharmaceutical composition to provide, without limitation, bulk, consistency, stability, binding ability, lubrication, disintegrating ability etc., to the composition. A "diluent" is a type of excipient.

[0127] The pharmaceutical compositions described herein can be administered to a human patient per se, or in pharmaceutical compositions where they are mixed with other active ingredients, as in combination therapy, or carriers, diluents, excipients or combinations thereof. Proper formulation is dependent upon the route of administration chosen. Techniques for formulation and administration of the compounds described herein are known to those skilled in the art.

[0128] The pharmaceutical compositions disclosed herein may be manufactured in a manner that is itself known, e.g., by means of conventional mixing, dissolving, granulating, dragee-making, levigating, emulsifying, encapsulating, entrapping or tableting processes. Additionally, the active ingredients are contained in an amount effective to achieve its intended purpose. Many of the compounds used in the pharmaceutical combinations disclosed herein may be provided as salts with pharmaceutically compatible counterions.

[0129] Multiple techniques of administering a compound exist in the art including, but not limited to, oral, rectal, topical, aerosol, injection and parenteral delivery, including intramuscular, subcutaneous, intravenous, intramedullary injections, intrathecal, direct intraventricular, intraperitoneal, intranasal and intraocular injections. [0130] One may also administer the compound in a local rather than systemic manner, for example, via injection of the compound directly into the infected area, often in a depot or sustained release formulation. Furthermore, one may administer the compound in a targeted drug delivery system, for example, in a liposome coated with a tissue-specific antibody. The liposomes will be targeted to and taken up selectively by the organ.

[0131] The compositions may, if desired, be presented in a pack or dispenser device which may contain one or more unit dosage forms containing the active ingredient. The pack may for example comprise metal or plastic foil, such as a blister pack. The pack or dispenser device may be accompanied by instructions for administration. The pack or dispenser may also be accompanied with a notice associated with the container in form prescribed by a governmental agency regulating the manufacture, use, or sale of pharmaceuticals, which notice is reflective of approval by the agency of the form of the drug for human or veterinary administration. Such notice, for example, may be the labeling approved by the U.S. Food and Drug Administration for prescription drugs, or the approved product insert. Compositions that can include a compound described herein formulated in a compatible pharmaceutical carrier may also be prepared, placed in an appropriate container, and labeled for treatment of an indicated condition.

Methods of Use

[0132] Some embodiments disclosed herein relate to a method of treating and/or ameliorating a disease or condition that can include administering to a subject a therapeutically effective amount of one or more compounds described herein, such as a compound of Formula (I), or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition that includes a compound described herein, or a pharmaceutically acceptable salt thereof. Other embodiments disclosed herein relate to a method of treating and/or ameliorating a disease or condition that can include administering to a subject identified as suffering from the disease or condition a therapeutically effective amount of one or more compounds described herein, such as a compound of Formula (I), or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition that includes a compound described herein, or a pharmaceutically acceptable salt thereof.

[0133] Some embodiments disclosed herein relates to a method of ameliorating or treating a HCV infection that can include administering to a subject identified as suffering from a HCV infection a therapeutically effective amount of one or more compounds described herein (for example, a compound of Formula (I)), or a pharmaceutical composition that includes one or more compounds described herein, or a pharmaceutically acceptable salt thereof. Other embodiments described herein relate to using one or more compounds described herein, or a pharmaceutically acceptable salt of a compound described herein, in the manufacture of a medicament for ameliorating and/or treating a HCV infection that can include administering to a subject identified as suffering from a HCV infection a therapeutically effective amount of one or more compounds described herein. Still other embodiments described herein relate to one or more compounds described herein, or a pharmaceutically acceptable salt of a compound described herein, that can be used for ameliorating and/or treating a HCV infection by administering to a subject identified as suffering from a HCV infection a therapeutically effective amount of one or more compounds described herein.

[0134] Some embodiments disclosed herein relate to methods of ameliorating and/or treating a HCV infection that can include contacting a cell infected with the hepatitis C virus with an effective amount of one or more compounds described herein, or a pharmaceutically acceptable salt of a compound described herein, or a pharmaceutical composition that includes one or more compounds described herein, or a pharmaceutically acceptable salt thereof. Other embodiments described herein relate to using one or more compounds described herein, or a pharmaceutically acceptable salt of a compound described herein, in the manufacture of a medicament for ameliorating and/or treating a HCV infection that can include contacting a cell infected with the hepatitis C virus with an effective amount of said compound(s). Still other embodiments described herein relate to one or more compounds described herein, or a pharmaceutically acceptable salt of a compound described herein, that can be used for ameliorating and/or treating a HCV infection by contacting a cell infected with the hepatitis C virus with an effective amount of said compound(s).

[0135] Some embodiments disclosed herein relate to methods of inhibiting replication of a hepatitis C virus that can include contacting a cell infected with the hepatitis C virus with an effective amount of one or more compounds described herein, or a pharmaceutically acceptable salt of a compound described herein, or a pharmaceutical composition that includes one or more compounds described herein, or a pharmaceutically acceptable salt thereof. Other embodiments described herein relate to using one or more compounds described herein, or a pharmaceutically acceptable salt of a compound described herein, in the manufacture of a medicament for inhibiting replication of a hepatitis C virus that can include contacting a cell infected with the hepatitis C virus with an effective amount of said compound(s). Still other embodiments described herein relate to a compound described herein, or a pharmaceutically acceptable salt of a compound described herein, that can be used for inhibiting replication of a hepatitis C virus by contacting a cell infected with the hepatitis C virus with an effective amount of said compound(s). In some embodiments, the compound of Formula (I), or a pharmaceutical acceptable salt thereof, that can be used to ameliorating and/or treating a viral infection (for example, a HCV infection) and/or inhibit replication of a virus (such as a HCV virus) can be any of the embodiments provided in any of the embodiments described in paragraphs [0090]-[0108].

[0136] In some embodiments, the compound can be a compound of Formula (I), or a pharmaceutical acceptable salt thereof, wherein R ³ is hydrogen. In other embodiments, the compound can be a compound of Formula (I), wherein compound of Formula (I) is a mono, di, or triphosphate, or a pharmaceutically acceptable salt of the foregoing. In still other embodiments, the compound can be a compound of Formula (I), wherein compound of Formula (I) is a thiomonophosphate, alpha-thiodiphosphate, or alpha-thiotriphosphate, or a pharmaceutically acceptable salt of the foregoing. In yet still other embodiments, the compound can be a compound of Formula (I), wherein compound of Formula (I) is phosphoramidate or phosphorbisamidate, or a pharmaceutically acceptable salt of the foregoing. In some embodiments, the compound can be a compound of Formula (I), wherein compound of Formula (I) is thiophosphoramidate or thiophosphorbisamidate, or a pharmaceutically acceptable salt of the foregoing.

[0137] HCV is an enveloped positive strand RNA virus in the Flaviviridae family. There are various nonstructural proteins of HCV, such as NS2, NS3, NS4, NS4A, NS4B, NS5A and NS5B. NS5B is believed to be an RNA-dependent RNA polymerase involved in the replication of HCV RNA.

[0138] Some embodiments described herein relate to a method of inhibiting NS5B polymerase activity that can include contacting a cell infected with hepatitis C virus with an effective amount of a compound of Formula (I), or a pharmaceutical acceptable salt thereof. Some embodiments described herein relate to a method of inhibiting NS5B polymerase activity that can include administering to a subject infected with hepatitis C virus an effective amount of a compound of Formula (I), or a pharmaceutical acceptable salt thereof. In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can inhibit a RNA dependent RNA polymerase, and thus, inhibit the replication of HCV RNA. In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can inhibit a HCV polymerase (for example, NS5B polymerase).

[0139] Some embodiments described herein relate to a method of treating a condition selected from liver fibrosis, liver cirrhosis and liver cancer in a subject suffering from one or more of the aforementioned liver conditions that can include administering to the subject an effective amount of a compound or a pharmaceutical composition described herein (for example, a compound of Formula (I), or a pharmaceutical acceptable salt thereof), wherein the liver condition is caused by a HCV infection. Some embodiments described herein relate to a method of increasing liver function in a subject having a HCV infection that can include administering to the subject an effective amount of a compound or a pharmaceutical composition described herein (for example, a compound of Formula (I), or a pharmaceutical acceptable salt thereof). Also contemplated is a method for reducing or eliminating further virus-caused liver damage in a subject having an HCV infection by administering to the subject an effective amount of a compound or a pharmaceutical composition described herein (for example, a compound of Formula (I), or a pharmaceutical acceptable salt thereof). In some embodiments, this method can include slowing or halting the progression of liver disease. In other embodiments, the course of the disease can be reversed, and stasis or improvement in liver function is contemplated. In some embodiments, liver fibrosis, liver cirrhosis and/or liver cancer can be treated; liver function can be increased; virus-caused liver damage can be reduced or eliminated; progression of liver disease can be slowed or halted; the course of the liver disease can be reversed and/or liver function can be improved or maintained by contacting a cell infected with hepatitis C virus with an effective amount of a compound described herein (for example, a compound of Formula (I), or a pharmaceutically acceptable salt thereof.)

[0140] There are a variety of genotypes of HCV, and a variety of subtypes within each genotype. For example, at present it is known that there are eleven (numbered 1 through 1 1) main genotypes of HCV, although others have classified the genotypes as 6 main genotypes. Each of these genotypes is further subdivided into subtypes (la-lc; 2a-2c; 3a-3b; 4a-4e; 5a; 6a; 7a- 7b; 8a-8b; 9a; 10a; and 1 la). In some embodiments, an effective amount of a compound of Formula (I), or a pharmaceutical acceptable salt thereof, or a pharmaceutical composition that includes an effective amount of a compound of Formula (I), or a pharmaceutical acceptable salt thereof, can be effective to treat at least one genotype of HCV. In some embodiments, a compound described herein (for example, a compound of Formula (I), or a pharmaceutical acceptable salt thereof) can be effective to treat all 1 1 genotypes of HCV. In some embodiments, a compound described herein (for example, a compound of Formula (I), or a pharmaceutical acceptable salt thereof) can be effective to treat 3 or more, 5 or more, 7 or more, or 9 or more genotypes of HCV. In some embodiments, a compound of Formula (I), or a pharmaceutical acceptable salt thereof can be more effective against a larger number of HCV genotypes than the standard of care. In some embodiments, a compound of Formula (I), or a pharmaceutical acceptable salt thereof, can be more effective against a particular HCV genotype than the standard of care (such as genotype 1, 2, 3, 4, 5 and/or 6).

[0141] Various indicators for determining the effectiveness of a method for treating a HCV infection are known to those skilled in the art. Examples of suitable indicators include, but are not limited to, a reduction in viral load, a reduction in viral replication, a reduction in time to seroconversion (virus undetectable in patient serum), an increase in the rate of sustained viral response to therapy, a reduction of morbidity or mortality in clinical outcomes, a reduction in the rate of liver function decrease; stasis in liver function; improvement in liver function; reduction in one or more markers of liver dysfunction, including alanine transaminase, aspartate transaminase, total bilirubin, conjugated bilirubin, gamma glutamyl transpeptidase and/or other indicator of disease response. Similarly, successful therapy with an effective amount of a compound or a pharmaceutical composition described herein (for example, a compound of Formula (I), or a pharmaceutical acceptable salt thereof) can reduce the incidence of liver cancer in HCV infected subjects.

[0142] In some embodiments, an effective amount of a compound of Formula (I), or a pharmaceutically acceptable salt thereof, is an amount that is effective to reduce HCV viral titers to undetectable levels, for example, to about 100 to about 500, to about 50 to about 100, to about 10 to about 50, or to about 15 to about 25 international units/mL serum. In some embodiments, an effective amount of a compound of Formula (I), or a pharmaceutically acceptable salt thereof, is an amount that is effective to reduce HCV viral load compared to the HCV viral load before administration of the compound of Formula (I), or a pharmaceutically acceptable salt thereof. For example, wherein the HCV viral load is measured before administration of the compound of Formula (I), or a pharmaceutically acceptable salt thereof, and again after completion of the treatment regime with the compound of Formula (I), or a pharmaceutically acceptable salt thereof (for example, 1 month after completion). In some embodiments, an effective amount of a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can be an amount that is effective to reduce HCV viral load to lower than about 25 international units/mL serum. In some embodiments, an effective amount of a compound of Formula (I), or a pharmaceutically acceptable salt thereof, is an amount that is effective to achieve a reduction in HCV viral titer in the serum of the subject in the range of about 1.5-log to about a 2.5-log reduction, about a 3-log to about a 4-log reduction, or a greater than about 5-log reduction compared to the viral load before administration of the compound of Formula (I), or a pharmaceutically acceptable salt thereof. For example, the HCV viral load can be measured before administration of the compound of Formula (I), or a pharmaceutically acceptable salt thereof, and again after completion of the treatment regime with the compound of Formula (I), or a pharmaceutically acceptable salt thereof (for example, 1 month after completion).

[0143] In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can result in at least a 1, 2, 3, 4, 5, 10, 15, 20, 25, 50, 75, 100-fold or more reduction in the replication of the hepatitis C virus relative to pre-treatment levels in a subject, as determined after completion of the treatment regime (for example 1 month after completion). In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can result in a reduction of the replication of the hepatitis C virus relative to pre-treatment levels in the range of about 2 to about 5 fold, about 10 to about 20 fold, about 15 to about 40 fold, or about 50 to about 100 fold. In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can result in a reduction of the hepatitis C virus replication in the range of 1 to 1.5 log, 1.5 log to 2 log, 2 log to 2.5 log, 2.5 to 3 log, 3 log to 3.5 log or 3.5 to 4 log more reduction of the hepatitis C virus replication compared to the reduction of the hepatitis C virus reduction achieved by pegylated interferon in combination with ribavirin, administered according to the standard of care, or may achieve the same reduction as that standard of care therapy in a shorter period of time, for example, in one month, two months, or three months, as compared to the reduction achieved after six months of standard of care therapy with ribavirin and pegylated interferon.

[0144] In some embodiments, an effective amount of a compound of Formula (I), or a pharmaceutically acceptable salt thereof, is an amount that is effective to achieve a sustained viral response, for example, non-detectable or substantially non-detectable HCV RNA (e.g., less than about 500, less than about 200, less than about 100, less than about 25, or less than about 15 international units per milliliter serum) is found in the subject's serum for a period of at least about one month, at least about two months, at least about three months, at least about four months, at least about five months, or at least about six months following cessation of therapy.

[0145] In some embodiments, a therapeutically effective amount of a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can reduce a level of a marker of liver fibrosis by at least about 10%, at least about 20%, at least about 25%, at least about 30%, at least about 35%, at least about 40%, at least about 45%, at least about 50%, at least about 55%, at least about 60%, at least about 65%, at least about 70%, at least about 75%, or at least about 80%, or more, compared to the level of the marker in an untreated subject, or to a placebo- treated subject. Methods of measuring serum markers are known to those skilled in the art and include immunological-based methods, e.g., enzyme-linked immunosorbent assays (ELISA), radioimmunoassays, and the like, using antibody specific for a given serum marker. A non- limiting list of examples of markers includes measuring the levels of serum alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP), gamma-glutamyl transpeptidase (GGT) and total bilirubin (TBIL) using known methods. In general, an ALT level of less than about 45 IU/L (international units/liter), an AST in the range of 10-34 IU/L, ALP in the range of 44-147 IU/L, GGT in the range of 0-51 IU/L, TBIL in the range of 0.3-1.9 mg/dL is considered normal. In some embodiments, an effective amount of a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can be an amount effective to reduce ALT, AST, ALP, GGT and/or TBIL levels to with what is considered a normal level.

[0146] Subjects who are clinically diagnosed with HCV infection include "naive" subjects (e.g., subjects not previously treated for HCV, particularly those who have not previously received IFN-alpha-based and/or ribavirin-based therapy) and individuals who have failed prior treatment for HCV ("treatment failure" subjects). Treatment failure subjects include "non-responders" (i.e., subjects in whom the HCV titer was not significantly or sufficiently reduced by a previous treatment for HCV (< 0.5 log IU/mL), for example, a previous IFN-alpha monotherapy, a previous IFN-alpha and ribavirin combination therapy, or a previous pegylated IFN-alpha and ribavirin combination therapy); and "relapsers" (i.e., subjects who were previously treated for HCV, for example, who received a previous IFN-alpha monotherapy, a previous IFN-alpha and ribavirin combination therapy, or a previous pegylated IFN-alpha and ribavirin combination therapy, whose HCV titer decreased, and subsequently increased).

[0147] In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can be administered to a treatment failure subject suffering from HCV. In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can be administered to a non-responder subject suffering from HCV. In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can be administered to a relapsed subject suffering from HCV.

[0148] After a period of time, infectious agents can develop resistance to one or more therapeutic agents. The term "resistance" as used herein refers to a viral strain displaying a delayed, lessened and/or null response to a therapeutic agent(s). For example, after treatment with an antiviral agent, the viral load of a subject infected with a resistant virus may be reduced to a lesser degree compared to the amount in viral load reduction exhibited by a subject infected with a non-resistant strain. In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can be administered to a subject infected with an HCV strain that is resistant to one or more different anti-HCV agents (for example, an agent used in a conventional standard of care). In some embodiments, development of resistant HCV strains is delayed when a subject is treated with a compound of Formula (I), or a pharmaceutically acceptable salt thereof, compared to the development of HCV strains resistant to other HCV drugs (such as a drug used in a conventional standard of care).

[0149] In some embodiments, an effective amount of a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can be administered to a subject for whom other anti- HCV medications are contraindicated. For example, administration of pegylated interferon alpha in combination with ribavirin is contraindicated in subjects with hemoglobinopathies (e.g., thalassemia major, sickle-cell anemia) and other subjects at risk from the hematologic side effects of current therapy. In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can be provided to a subject that is hypersensitive to interferon and/or ribavirin.

[0150] Some subjects being treated for HCV experience a viral load rebound. The term "viral load rebound" as used herein refers to a sustained >0.5 log IU/mL increase of viral load above nadir before the end of treatment, where nadir is a >0.5 log IU/mL decrease from baseline. In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can be administered to a subject experiencing viral load rebound, or can prevent such viral load rebound when used to treat the subject.

[0151] The standard of care for treating HCV has been associated with several side effects (adverse events). In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can decrease the number and/or severity of side effects that can be observed in HCV patients being treated with ribavirin and pegylated interferon according to the standard of care. Examples of side effects include, but are not limited to fever, malaise, tachycardia, chills, headache, arthralgias, myalgias, fatigue, apathy, loss of appetite, nausea, vomiting, cognitive changes, asthenia, drowsiness, lack of initiative, irritability, confusion, depression, severe depression, suicidal ideation, anemia, low white blood cell counts, and thinning of hair. In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can be provided to a subject that discontinued a HCV therapy because of one or more adverse effects or side effects associated with one or more other HCV agents (for example, an agent used in a conventional standard of care).

[0152] Table 1 provides some embodiments of the percentage improvement obtained using a compound of Formula (I), or a pharmaceutically acceptable salt thereof, as compared to the standard of care. Examples include the following: in some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, results in a percentage of non- responders that is 10% less than the percentage of non-responders receiving the standard of care; in some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, results in a number of side effects that is in the range of about 10% to about 30% less than compared to the number of side effects experienced by a subject receiving the standard of care; and in some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, results in a severity of a side effect (such as one of those described herein) that is 25% less than compared to the severity of the same side effect experienced by a subject receiving the standard of care. Methods of quantifying the severity of a side effect are known to those skilled in the art.

Table 1

[0153] As used herein, a "subject" refers to an animal that is the object of treatment, observation or experiment. "Animal" includes cold- and warm-blooded vertebrates and invertebrates such as fish, shellfish, reptiles and, in particular, mammals. "Mammal" includes, without limitation, mice, rats, rabbits, guinea pigs, dogs, cats, sheep, goats, cows, horses, primates, such as monkeys, chimpanzees, and apes, and, in particular, humans. In some embodiments, the subject is human. [0154] As used herein, the terms "treating," "treatment," "therapeutic," or "therapy" do not necessarily mean total cure or abolition of the disease or condition. Any alleviation of any undesired signs or symptoms of a disease or condition, to any extent can be considered treatment and/or therapy. Furthermore, treatment may include acts that may worsen the patient's overall feeling of well-being or appearance.

[0155] The terms "therapeutically effective amount" and "effective amount" are used to indicate an amount of an active compound, or pharmaceutical agent, that elicits the biological or medicinal response indicated. For example, a therapeutically effective amount of compound can be the amount needed to prevent, alleviate or ameliorate symptoms of disease or prolong the survival of the subject being treated This response may occur in a tissue, system, animal or human and includes alleviation of the signs or symptoms of the disease being treated. Determination of a therapeutically effective amount is well within the capability of those skilled in the art, in view of the disclosure provided herein. The therapeutically effective amount of the compounds disclosed herein required as a dose will depend on the route of administration, the type of animal, including human, being treated, and the physical characteristics of the specific animal under consideration. The dose can be tailored to achieve a desired effect, but will depend on such factors as weight, diet, concurrent medication and other factors which those skilled in the medical arts will recognize.

[0156] As will be readily apparent to one skilled in the art, the useful in vivo dosage to be administered and the particular mode of administration will vary depending upon the age, weight, the severity of the affliction, and mammalian species treated, the particular compounds employed, and the specific use for which these compounds are employed. The determination of effective dosage levels, that is the dosage levels necessary to achieve the desired result, can be accomplished by one skilled in the art using routine methods, for example, human clinical trials and in vitro studies.

[0157] The dosage may range broadly, depending upon the desired effects and the therapeutic indication. Alternatively dosages may be based and calculated upon the surface area of the patient, as understood by those of skill in the art. Although the exact dosage will be determined on a drug-by-drug basis, in most cases, some generalizations regarding the dosage can be made. The daily dosage regimen for an adult human patient may be, for example, an oral dose of between 0.01 mg and 3000 mg of each active ingredient, preferably between 1 mg and 700 mg, e.g. 5 to 200 mg. The dosage may be a single one or a series of two or more given in the course of one or more days, as is needed by the subject. In some embodiments, the compounds will be administered for a period of continuous therapy, for example for a week or more, or for months or years. In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can be administered less frequently compared to the frequency of administration of an agent within the standard of care. In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can be administered one time per day. For example, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can be administered one time per day to a subject suffering from a HCV infection. In some embodiments, the total time of the treatment regime with a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can less compared to the total time of the treatment regime with the standard of care.

[0158] In instances where human dosages for compounds have been established for at least some condition, those same dosages may be used, or dosages that are between about 0.1% and 500%, more preferably between about 25% and 250% of the established human dosage. Where no human dosage is established, as will be the case for newly-discovered pharmaceutical compositions, a suitable human dosage can be inferred from ED5 ₀ or ID ₅₀ values, or other appropriate values derived from in vitro or in vivo studies, as qualified by toxicity studies and efficacy studies in animals.

[0159] In cases of administration of a pharmaceutically acceptable salt, dosages may be calculated as the free base. As will be understood by those of skill in the art, in certain situations it may be necessary to administer the compounds disclosed herein in amounts that exceed, or even far exceed, the above-stated, preferred dosage range in order to effectively and aggressively treat particularly aggressive diseases or infections.

[0160] Dosage amount and interval may be adjusted individually to provide plasma levels of the active moiety which are sufficient to maintain the modulating effects, or minimal effective concentration (MEC). The MEC will vary for each compound but can be estimated from in vitro data. Dosages necessary to achieve the MEC will depend on individual characteristics and route of administration. However, HPLC assays or bioassays can be used to determine plasma concentrations. Dosage intervals can also be determined using MEC value. Compositions should be administered using a regimen which maintains plasma levels above the MEC for 10-90% of the time, preferably between 30-90% and most preferably between 50-90%. In cases of local administration or selective uptake, the effective local concentration of the drug may not be related to plasma concentration.

[0161] It should be noted that the attending physician would know how to and when to terminate, interrupt, or adjust administration due to toxicity or organ dysfunctions. Conversely, the attending physician would also know to adjust treatment to higher levels if the clinical response were not adequate (precluding toxicity). The magnitude of an administrated dose in the management of the disorder of interest will vary with the severity of the condition to be treated and to the route of administration. The severity of the condition may, for example, be evaluated, in part, by standard prognostic evaluation methods. Further, the dose and perhaps dose frequency, will also vary according to the age, body weight, and response of the individual patient. A program comparable to that discussed above may be used in veterinary medicine.

[0162] Compounds disclosed herein can be evaluated for efficacy and toxicity using known methods. For example, the toxicology of a particular compound, or of a subset of the compounds, sharing certain chemical moieties, may be established by determining in vitro toxicity towards a cell line, such as a mammalian, and preferably human, cell line. The results of such studies are often predictive of toxicity in animals, such as mammals, or more specifically, humans. Alternatively, the toxicity of particular compounds in an animal model, such as mice, rats, rabbits, or monkeys, may be determined using known methods. The efficacy of a particular compound may be established using several recognized methods, such as in vitro methods, animal models, or human clinical trials. When selecting a model to determine efficacy, the skilled artisan can be guided by the state of the art to choose an appropriate model, dose, route of administration and/or regime.

Combination Therapies

[0163] In some embodiments, the compounds disclosed herein, such as a compound of Formula (I), or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition that includes a compound described herein, or a pharmaceutically acceptable salt thereof, can be used in combination with one or more additional agent(s). Examples of additional agents that can be used in combination with a compound of Formula (I), or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition that includes a compound of Formula (I), or a pharmaceutically acceptable salt thereof, include, but are not limited to, agents currently used in a conventional standard of care for treating HCV, HCV protease inhibitors, HCV polymerase inhibitors, NS5A inhibitors, other antiviral compounds, compounds of Formula (AA), (including pharmaceutically acceptable salts and pharmaceutical compositions that can include a compound of Formula (AA), or a pharmaceutically acceptable salt thereof), compounds of Formula (BB) (including pharmaceutically acceptable salts and pharmaceutical compositions that can include a compound of Formula (BB), or a pharmaceutically acceptable salt thereof), compounds of Formula (CC) (including pharmaceutically acceptable salts and pharmaceutical compositions that can include a compound of Formula (CC), or a pharmaceutically acceptable salt thereof), and/or combinations thereof. In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition that includes a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can be used with one, two, three or more additional agents described herein. A non-limiting list of examples of combinations of a compound of Formula (I), or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition that includes a compound of Formula (I), or a pharmaceutically acceptable salt thereof, is provided in Tables A, B, C, D and E.

[0164] In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition that includes a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can be used in combination with an agent(s) currently used in a conventional standard of care therapy. For example, for the treatment of HCV, a compound disclosed herein can be used in combination with Pegylated interferon-alpha- 2a (brand name PEGASYS®) and ribavirin, or Pegylated interferon-alpha-2b (brand name PEG- INTRON®) and ribavirin.

[0165] In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition that includes a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can be substituted for an agent currently used in a conventional standard of care therapy. For example, for the treatment of HCV, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition that includes a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can be used in place of ribavirin.

[0166] In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition that includes a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can be used in combination with an interferon, such as a pegylated interferon. Examples of suitable interferons include, but are not limited to, Pegylated interferon-alpha-2a (brand name PEGASYS®), Pegylated interferon-alpha-2b (brand name PEG-INTRON®), interferon alfacon-1 (brand name INFERGEN®), pegylated interferon lambda and/or a combination thereof.

[0167] In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition that includes a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can be used in combination with a HCV protease inhibitor. A non-limiting list of example HCV protease inhibitors include the following: VX-950 (TELAPREVIR®), MK-5172, ABT-450, BILN-2061, BI-201335, BMS- 650032, SCH 503034 (BOCEPREVIR®), GS-9256, GS-9451, IDX-320, ACH-1625, ACH- 2684, TMC-435, ITMN-191 (DANOPREVIR®) and/or a combination thereof. Additional HCV protease inhibitors suitable for use in combination with a compound of Formula (I), or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition that includes a compound of Formula (I), or a pharmaceutically acceptable salt thereof, include VP-19744, PSI- 879, VCH-759/VX-759, HCV-371, IDX-375, GL-60667, JTK-109, PSI-6130, R1479, R-1626, R-7182, MK-0608, ΓΝΧ-8014, ΓΝΧ-8018, A-848837, A-837093, BILB-1941, VCH-916, VCH- 716, GSK-71 185, GSK-625433, XTL-2125 and those disclosed in PCT Publication No. WO 2012/142085, which is hereby incorporated by reference for the limited purpose of its disclosure of HCV protease inhibitors, HCV polymerase inhibitors and NS5A inhibitors. A non-limiting list of example HCV protease inhibitors includes the compounds numbered 1001-1016 in Figure 1.

[0168] In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition that includes a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can be used in combination with a HCV polymerase inhibitor. In some embodiments, the HCV polymerase inhibitor can be a nucleoside inhibitor. In other embodiments, the HCV polymerase inhibitor can be a non-nucleoside inhibitor. Examples of suitable nucleoside inhibitors include, but are not limited to, RG7128, PSI-7851, PSI-7977, ΓΝΧ-189, PSI-352938, PSI-661, 4'-azidouridine (including known prodrugs of 4'-azidouridine), GS-6620, IDX-184, and TMC649128 and/or combinations thereof. A non-limiting list of example nucleoside inhibitors includes compounds numbered 2001-2012 in Figure 2. Examples of suitable non-nucleoside inhibitors include, but are not limited to, ABT-333, ANA-598, VX-222, HCV-796, BI-207127, GS-9190, PF-00868554 (FILIBUVIR®), VX-497 and/or combinations thereof. A non-limiting list of example non-nucleoside inhibitors includes the compounds numbered 3001-3014 in Figure 3. Further HCV polymerase inhibitors suitable for use in combination with a compound of Formula (I), or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition that includes a compound of Formula (I), or a pharmaceutically acceptable salt thereof, include VX-500, VX-813, VBY-376, TMC- 435350, EZ-058, EZ-063, GS-9132, ACH-1095, IDX-136, IDX-316, ITMN-8356, ITMN-8347, ITMN-8096, ITMN-7587, VX-985, and those disclosed in PCT Publication No. WO 2012/142085.

[0169] In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition that includes a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can be used in combination with a NS5A inhibitor. Examples of NS5A inhibitors include BMS-790052, PPI-461, ACH-2928, GS-5885, BMS-824393 and/or combinations thereof. A non-limiting list of example NS5A inhibitors includes the compounds numbered 4001-4012 in Figure 4. Additional NS5A inhibitors suitable for use in combination with a compound of Formula (I), or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition that includes a compound of Formula (I), or a pharmaceutically acceptable salt thereof, include A-832, PPI-1301 and those disclosed in PCT Publication No. WO 2012/142085.

[0170] In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition that includes a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can be used in combination with other antiviral compounds. Examples of other antiviral compounds include, but are not limited to, Debio-025, MIR- 122, cyclosporin A and/or combinations thereof. A non-limiting list of example other antiviral compounds includes the compounds numbered 5001-5012 in Figure 5.

[0171] In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition that includes a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can be used in combination with a compound of Formula (AA), or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition that includes a compound of Formula (AA), or a pharmaceutically acceptable salt thereof (see, U.S. Publication No. 2013/0164261, filed June 27, 2013, the contents of which are incorporated by reference in its entirety):

Formula (AA) wherein: B^ ¹ can be an optionally substituted heterocyclic base or an optionally substituted heterocyclic base with a protected amino group; R^ ¹ can be selected from O ^" , OH, an optionally substituted N-linked amino acid and an optionally substituted N-linked amino acid ester derivative; R^ ² can be absent or selected from hydrogen, an optionally substituted aryl, an optionally substituted heteroaryl, an optionally substituted heterocyclyl and

can be independently absent or hydrogen, and n^ can be 0 or 1; provided that when R^ ¹ is O ^" or OH, then R^ ² is absent, hydrogen or can be selected from hydrogen, halogen,

OR ^AA9 and -OC(=0)R ^AA1 °; R^ ⁴ can be selected from halogen, -OR^ ¹¹ and -OC(=0)R ^AA12 ;or R ^AA3 and R^ ⁴ can be both an oxygen atom which are linked together by a carbonyl group; R ^AA5 can be selected from an optionally substituted C2-6 alkyl, an optionally substituted C2-6 alkenyl, an optionally substituted C2-6 alkynyl and an optionally substituted C3-6 cycloalkyl; or R^ ⁴ and R ^AA5 together can form -(Ci_ ₆ alkyl)-0- or -0-(C _1-6 alkyl)-; R^ ⁹ and R ^AA11 can be independently hydrogen or an optionally substituted Ci-6 alkyl; and R^ ¹⁰ and R ^AA12 can be independently an optionally substituted Ci_6 alkyl or an optionally substituted C3-6 cycloalkyl. A non-limiting list of examples of compounds of Formula (AA) includes the compounds numbered 7000-7027 in Figure 7.

[0172] In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition that includes a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can be used in combination with a compound of Formula (BB), or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition that includes a compound of Formula (BB), or a pharmaceutically acceptable salt thereof (see, U.S. Publication No. 2012/0165286, published June 28, 2012, the contents of which are incorporated by reference in their entireties):

Formula (BB) wherein B ^BB1 can be an optionally substituted heterocyclic base or an optionally substituted heterocyclic base with a protected amino group; X ^BB can be O (oxygen) or S (sulfur); R ^BB1 can be selected from -Z ^BB -R ^BB9 , an optionally substituted N-linked amino acid and an optionally substituted N-linked amino acid ester derivative; Z ^BB can be selected from O (oxygen), S (sulfur) and N(R ^BB1 °); R ^BB2 and R ^BB3 can be independently selected from hydrogen, an optionally substituted Ci_6 alkyl, an optionally substituted C2-6 alkenyl, an optionally substituted C2-6 alkynyl, an optionally substituted Ci_6 haloalkyl and an optionally substituted aryl(Ci_6 alkyl); or R ^BB2 and R ^BB3 can be taken together to form a group selected from an optionally substituted C3-6 cycloalkyl, an optionally substituted C3-6 cycloalkenyl, an optionally substituted C3-6 aryl and an optionally substituted C3-6 heteroaryl; R ^BB4 can be selected from hydrogen, halogen, azido, cyano, an optionally substituted Ci_6 alkyl, an optionally substituted C2-6 alkenyl, an optionally substituted C2-6 alkynyl and an optionally substituted allenyl; R ^BB5 can be hydrogen or an optionally substituted Ci_6 alkyl; R ^BB6 can be selected from hydrogen, halogen, azido, amino, cyano, an optionally substituted Ci_ ₆ alkyl, -OR ^BB11 and -OC(=0)R ^BB12 ; R ^BB? can be selected from hydrogen, halogen, azido, cyano, an optionally substituted Ci_6 alkyl, -OR ^BB13 and -OC(=0)R ^BB14 ; R ^BB8 can be selected from hydrogen, halogen, azido, cyano, an optionally substituted Ci_ ₆ alkyl, -OR ^BB15 and -OC(=0)R ^BB16 ; R ^BB9 can be selected from an optionally substituted alkyl, an optionally substituted alkenyl, an optionally substituted alkynyl, an optionally substituted cycloalkyl, an optionally substituted cycloalkenyl, an optionally substituted aryl, an optionally substituted heteroaryl, an optionally substituted heterocyclyl, an optionally substituted aryl(Ci_ ₆ alkyl), an optionally substituted heteroaryl(Ci_ ₆ alkyl) and an optionally substituted heterocyclyl(Ci_ ₆ alkyl); R ^BB1 ° _ca n be selected from hydrogen, an optionally substituted alkyl, an optionally substituted alkenyl, an optionally substituted alkynyl, an optionally substituted cycloalkyl, an optionally substituted cycloalkenyl, an optionally substituted aryl, an optionally substituted heteroaryl, an optionally substituted heterocyclyl, an optionally substituted aryl(Ci_ ₆ alkyl), an optionally substituted heteroaryl(Ci_ ₆ alkyl) and an optionally substituted heterocyclyl(Ci_ ₆ alkyl); R ^BB11 , R ^BB13 and R ^BB15 can be independently hydrogen or an optionally substituted Ci_6 alkyl; and R ^BB12 , R ^BB14 and R ^BB16 can be independently an optionally substituted Ci_6 alkyl or an optionally substituted C3-6 cycloalkyl. In some embodiments, at least one of R ^BB2 and R ^BB3 is not hydro gen. A non-limiting list of example compounds of Formula (BB) includes the compound numbered 8000-8016 in Figure 8.

[0173] In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition that includes a compound of Formula

(I), or a pharmaceutically acceptable salt thereof, can be used in combination with a compound of Formula (CC), or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition that includes a compound of Formula (CC), or a pharmaceutically acceptable salt thereof (see,

U.S. Publication No. 2012/0071434, published March 22, 2012, the contents of which are incorporated by reference in its entirety):

Formula (CC) wherein B can be an optionally substituted heterocyclic base or an optionally substituted heterocyclic base with a protected amino group; R ^CC1 can be selected from O ^" , OH, an optionally substituted N-linked amino acid and an optionally substituted N-linked amino acid ester derivative; R can be selected from an optionally substituted aryl, an optionally substituted

heteroaryl, an optionally substituted heterocyclyl and , wherein

R , R and R can be independently absent or hydrogen, and n can be 0 or 1;

provided that when R ^LL1 is O ^" or OH, then R ^CC3a and

R ^CC3b can be independently selected from hydrogen, deuterium, an optionally substituted Ci_6 alkyl, an optionally substituted C2-6 alkenyl, an optionally substituted C2-6 alkynyl, an optionally substituted Ci_6 haloalkyl and aryl(Ci_6 alkyl); or R and R can be taken together to form an optionally substituted C3-6 cycloalkyl; R ^CC4 can be selected from hydrogen, azido, an optionally substituted Ci_6 alkyl, an optionally substituted C2-6 alkenyl and an optionally substituted C2-6 alkynyl; R ^CC5 can be selected from hydrogen, halogen, azido, cyano, an optionally substituted Ci_ ₆ alkyl, -OR ^CC10 and -OC(=0)R ^ccn ; R ^CC6 can be selected from hydrogen, halogen, azido, cyano, an optionally substituted Ci_6 alkyl, -OR ^CC12 and -

> CC7

OC(=0)R ^CC13 ; R^' can be selected from hydrogen, halogen, azido, cyano, an optionally

CC15. , CC6 , CC7

substituted Ci_ ₆ alkyl, -OR ^CC14 and -OC(=0)R^ ¹³ ; or R^° and R^' can be both oxygen atoms and linked together by a carbonyl group; R ^CC8 can be selected from hydrogen, halogen, azido, cyano, an optionally substituted Ci_ ₆ alkyl, -OR ^CC16 and -OC(=0)R ^CC17 ; R ^CC9 can be selected

CCl 8 CC10 CCl 2 from hydrogen, azido, cyano, an optionally substituted Ci_6 alkyl and -OR ; R , R ,

_R CC14 _R CC16 _R CC18 can be independently selected from hydrogen and an optionally substituted Ci_ ₆ alkyl; and R ^ccu , R ^CC13 , R ^CC15 and R ^CC1? can be independently selected from an optionally substituted Ci_6 alkyl and an optionally substituted C3-6 cycloalkyl. In some embodiments, when R ^CC3a , R ^CC3b , R ^CC4 , R ^CC5 , R ^CC7 , R ^CC8 and R ^CC9 are all hydrogen, then R ^CC6 is

not azido. In some embodiments, R cannot be when R ^CC3a is hydrogen, R^ ^3b is hydrogen, R is H, R is OH or H, R is hydrogen, OH, or - OC(=0)CH ₃ , R ^cc? is hydrogen, OH, OCH ₃ or -OC(=0)CH ₃ , R ^CC8 is hydrogen, OH or OCH ₃ , R^ ^y is H and B is an optionally substituted adenine, an optionally substituted guanine, an optionally substituted uracil or an optionally substituted hypoxanthine. In some embodiments,

R cannot be A non-limiting list of examples of compounds of Formula (CC) includes the compounds numbered 6000-6078 in Figure 6.

[0174] Some embodiments described herein relate to a method of ameliorating or treating a HCV infection that can include contacting a cell infected with the HCV infection with a therapeutically effective amount of a compound of Formula (I), or a pharmaceutically acceptable salt thereof, in combination with one or more agents selected from an interferon, ribavirin, a HCV protease inhibitor, a HCV polymerase inhibitor, a NS5A inhibitor, an antiviral compound, a compound of Formula (AA), a compound of Formula (BB) and a compound of Formula (CC), or a pharmaceutically acceptable salt of any of the aforementioned compounds.

[0175] Some embodiments described herein relate to a method of ameliorating or treating a HCV infection that can include administering to a subject suffering from the HCV infection a therapeutically effective amount of a compound of Formula (I), or a pharmaceutically acceptable salt thereof, in combination with one or more agents selected from an interferon, ribavirin, a HCV protease inhibitor, a HCV polymerase inhibitor, a NS5A inhibitor, an antiviral compound, a compound of Formula (AA), a compound of Formula (BB) and a compound of Formula (CC), or a pharmaceutically acceptable salt of any of the aforementioned compounds.

[0176] Some embodiments described herein relate to a method of inhibiting the replication of a hepatitis C virus that can include contacting a cell infected with the hepatitis C virus with an effective amount of a compound of Formula (I), or a pharmaceutically acceptable salt thereof, in combination with one or more agents selected from an interferon, ribavirin, a HCV protease inhibitor, a HCV polymerase inhibitor, a NS5A inhibitor, an antiviral compound, a compound of Formula (AA), a compound of Formula (BB) and a compound of Formula (CC), or a pharmaceutically acceptable salt of any of the aforementioned compounds.

[0177] Some embodiments described herein relate to a method of inhibiting the replication of a hepatitis C virus that can include administering to a subject infected with the hepatitis C virus an effective amount of a compound of Formula (I), or a pharmaceutically acceptable salt thereof, in combination with one or more agents selected from an interferon, ribavirin, a HCV protease inhibitor, a HCV polymerase inhibitor, a NS5A inhibitor, an antiviral compound, a compound of Formula (AA), a compound of Formula (BB) and a compound of Formula (CC), or a pharmaceutically acceptable salt of any of the aforementioned compounds. [0178] In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can be administered with one or more additional agent(s) together in a single pharmaceutical composition. In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt the thereof, can be administered with one or more additional agent(s) as two or more separate pharmaceutical compositions. For example, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can be administered in one pharmaceutical composition, and at least one of the additional agents can be administered in a second pharmaceutical composition. If there are at least two additional agents, one or more of the additional agents can be in a first pharmaceutical composition that includes a compound of Formula (I), or a pharmaceutically acceptable salt thereof, and at least one of the other additional agent(s) can be in a second pharmaceutical composition.

[0179] The dosing amount(s) and dosing schedule(s) when using a compound of Formula (I), or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition that includes a compound of Formula (I), or a pharmaceutically acceptable salt thereof, and one or more additional agents are within the knowledge of those skilled in the art. For example, when performing a conventional standard of care therapy using art-recognized dosing amounts and dosing schedules, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition that includes a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can be administered in addition to that therapy, or in place of one of the agents of a combination therapy, using effective amounts and dosing protocols as described herein.

[0180] The order of administration of a compound of Formula (I), or a pharmaceutically acceptable salt thereof, with one or more additional agent(s) can vary. In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can be administered prior to all additional agents. In other embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can be administered prior to at least one additional agent. In still other embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can be administered concomitantly with one or more additional agent(s). In yet still other embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can be administered subsequent to the administration of at least one additional agent. In some embodiments, a compound of Formula (I), or a pharmaceutically acceptable salt thereof, can be administered subsequent to the administration of all additional agents.

[0181] In some embodiments, the combination of a compound of Formula (I), or a pharmaceutically acceptable salt thereof, in combination with one or more additional agent(s) in Figures 1-8 (including pharmaceutically acceptable salts and prodrugs thereof) can result in an additive effect. In some embodiments, the combination of a compound of Formula (I), or a pharmaceutically acceptable salt thereof, in combination with one or more additional agent(s) in Figures 1-8 (including pharmaceutically acceptable salts and prodrugs thereof) can result in a synergistic effect. In some embodiments, the combination of a compound of Formula (I), or a pharmaceutically acceptable salt thereof, in combination with one or more additional agent(s) in Figures 1-8 (including pharmaceutically acceptable salts and prodrugs thereof) can result in a strongly synergistic effect. In some embodiments, the combination of a compound of Formula (I), or a pharmaceutically acceptable salt thereof, in combination with one or more additional agent(s) in Figures 1-8 (including pharmaceutically acceptable salts and prodrugs thereof) is not antagonistic.

[0182] As used herein, the term "antagonistic" means that the activity of the combination of compounds is less compared to the sum of the activities of the compounds in combination when the activity of each compound is determined individually (i.e. as a single compound). As used herein, the term "synergistic effect" means that the activity of the combination of compounds is greater than the sum of the individual activities of the compounds in the combination when the activity of each compound is determined individually. As used herein, the term "additive effect" means that the activity of the combination of compounds is about equal to the sum of the individual activities of the compound in the combination when the activity of each compound is determined individually.

[0183] A potential advantage of utilizing a compound of Formula (I), or a pharmaceutically acceptable salt thereof, in combination with one or more additional agent(s) in Figures 1-8 (including pharmaceutically acceptable salts thereof) may be a reduction in the required amount(s) of one or more compounds of Figures 1-8 (including pharmaceutically acceptable salts thereof) that is effective in treating a disease condition disclosed herein (for example, HCV), as compared to the amount required to achieve same therapeutic result when one or more compounds of Figures 1-8 (including pharmaceutically acceptable salts thereof) are administered without a compound of Formula (I), or a pharmaceutically acceptable salt thereof. For example, the amount of a compound in Figures 1-8 (including a pharmaceutically acceptable salt thereof), can be less compared to the amount of the compound in Figures 1-8 (including a pharmaceutically acceptable salt thereof), needed to achieve the same viral load reduction when administered as a monotherapy. Another potential advantage of utilizing a compound of Formula (I), or a pharmaceutically acceptable salt thereof, in combination with one or more additional agent(s) in Figures 1-8 (including pharmaceutically acceptable salts thereof) is that the use of two or more compounds having different mechanism of actions can create a higher barrier to the development of resistant viral strains compared to the barrier when a compound is administered as monotherapy.

[0184] Additional advantages of utilizing a compound of Formula (I), or a pharmaceutically acceptable salt thereof, in combination with one or more additional agent(s) in Figures 1-8 (including pharmaceutically acceptable salts thereof) may include little to no cross resistance between a compound of Formula (I), or a pharmaceutically acceptable salt thereof, and one or more additional agent(s) in Figures 1 -8 (including pharmaceutically acceptable salts thereof) thereof; different routes for elimination of a compound of Formula (I), or a pharmaceutically acceptable salt thereof, and one or more additional agent(s) in Figures 1-8 (including pharmaceutically acceptable salts thereof); little to no overlapping toxicities between a compound of Formula (I), or a pharmaceutically acceptable salt thereof, and one or more additional agent(s) in Figures 1-8 (including pharmaceutically acceptable salts thereof); little to no significant effects on cytochrome P450; little to no pharmacokinetic interactions between a compound of Formula (I), or a pharmaceutically acceptable salt thereof, and one or more additional agent(s) in Figures 1-8 (including pharmaceutically acceptable salts thereof); greater percentage of subjects achieving a sustained viral response compared to when a compound is administered as monotherapy and/or a decrease in treatment time to achieve a sustained viral response compared to when a compound is administered as monotherapy.

[0185] A non-limiting list of example combination of compounds of Formula (I), or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition that includes a compound described herein, with one or more additional agent(s) are provided in Tables A, B, C, D and E. Each numbered X and Y compound in Tables A, B, C, D and E has a corresponding name and/or structure provided in Figures 1-8. The numbered compounds in Tables A, B, C, D and E includes pharmaceutically acceptable salts of the compounds and pharmaceutical compositions containing the compounds or a pharmaceutically acceptable salt thereof. For example, 1001 includes the compound corresponding to 1001, pharmaceutically acceptable salts thereof, and pharmaceutical compositions that include compound 1001 and/or a pharmaceutically acceptable salt thereof. The combinations exemplified in Tables A, B, C, D and E are designated by the formula X:Y, which represents a combination of a compound X with a compound Y. For example, the combination designated as 1001 :9002 in Table A represents a combination of compound 1001 with compound 9002, including pharmaceutically acceptable salts of compound 1001 and/or 9002, and pharmaceutical compositions including compound 1001 and 9002 (including pharmaceutical compositions that include pharmaceutically acceptable salts of compound 1001 and/or compound 9002). Thus, the combination designated as 1001 : 9002 in Table A represents the combination of Telaprevir

(compound 1001, as shown in Figure 1) and (compound 9002

, as shown in Figure 9), including pharmaceutically acceptable salts of compound 1001 and/or 9002, and pharmaceutical compositions including compound 1001 and 9002 (including pharmaceutical compositions that include pharmaceutically acceptable salts of compound 1001 and/or compound 9002). Each of the combinations provided in Tables A, B, C, D and E can be used with one, two, three or more additional agents described herein. In some embodiments described herein, the combination of agents can be used to treat, ameliorate and/or inhibit a virus and/or a viral infection, wherein the virus can be HCV and the viral infection can be an HCV viral infection.

Table A: Example combinations of a compound X with a compound Y.

X Y X Y X Y X Y X Y X Y

1001 9000 1001 9001 1001 9002 1001 9003 1001 9004 1001 9005

1002 9000 1002 9001 1002 9002 1002 9003 1002 9004 1002 9005

1003 9000 1003 9001 1003 9002 1003 9003 1003 9004 1003 9005

1004 9000 1004 9001 1004 9002 1004 9003 1004 9004 1004 9005

1005 9000 1005 9001 1005 9002 1005 9003 1005 9004 1005 9005

1006 9000 1006 9001 1006 9002 1006 9003 1006 9004 1006 9005

1007 9000 1007 9001 1007 9002 1007 9003 1007 9004 1007 9005

1008 9000 1008 9001 1008 9002 1008 9003 1008 9004 1008 9005

1009 9000 1009 9001 1009 9002 1009 9003 1009 9004 1009 9005

1010 9000 1010 9001 1010 9002 1010 9003 1010 9004 1010 9005

1011 9000 1011 9001 1011 9002 1011 9003 1011 9004 1011 9005

1012 9000 1012 9001 1012 9002 1012 9003 1012 9004 1012 9005

1013 9000 1013 9001 1013 9002 1013 9003 1013 9004 1013 9005

1014 9000 1014 9001 1014 9002 1014 9003 1014 9004 1014 9005

1015 9000 1015 9001 1015 9002 1015 9003 1015 9004 1015 9005

1016 9000 1016 9001 1016 9002 1016 9003 1016 9004 1016 9005

2001 9000 2001 9001 2001 9002 2001 9003 2001 9004 2001 9005

2002 9000 2002 9001 2002 9002 2002 9003 2002 9004 2002 9005

2003 9000 2003 9001 2003 9002 2003 9003 2003 9004 2003 9005

2004 9000 2004 9001 2004 9002 2004 9003 2004 9004 2004 9005

2005 9000 2005 9001 2005 9002 2005 9003 2005 9004 2005 9005

2006 9000 2006 9001 2006 9002 2006 9003 2006 9004 2006 9005

2007 9000 2007 9001 2007 9002 2007 9003 2007 9004 2007 9005

2008 9000 2008 9001 2008 9002 2008 9003 2008 9004 2008 9005

2009 9000 2009 9001 2009 9002 2009 9003 2009 9004 2009 9005

2010 9000 2010 9001 2010 9002 2010 9003 2010 9004 2010 9005

2011 9000 2011 9001 2011 9002 2011 9003 2011 9004 2011 9005

2012 9000 2012 9001 2012 9002 2012 9003 2012 9004 2012 9005

X Y X Y X Υ X Υ X Υ X Υ

1001 9006 1001 9007 1001 9008 1001 9009 1001 9010 1001 9011

1002 9006 1002 9007 1002 9008 1002 9009 1002 9010 1002 9011

1003 9006 1003 9007 1003 9008 1003 9009 1003 9010 1003 9011

1004 9006 1004 9007 1004 9008 1004 9009 1004 9010 1004 9011

1005 9006 1005 9007 1005 9008 1005 9009 1005 9010 1005 9011

1006 9006 1006 9007 1006 9008 1006 9009 1006 9010 1006 9011

1007 9006 1007 9007 1007 9008 1007 9009 1007 9010 1007 9011

1008 9006 1008 9007 1008 9008 1008 9009 1008 9010 1008 9011

1009 9006 1009 9007 1009 9008 1009 9009 1009 9010 1009 9011

1010 9006 1010 9007 1010 9008 1010 9009 1010 9010 1010 9011

1011 9006 1011 9007 1011 9008 1011 9009 1011 9010 1011 9011

1012 9006 1012 9007 1012 9008 1012 9009 1012 9010 1012 9011

1013 9006 1013 9007 1013 9008 1013 9009 1013 9010 1013 9011

1014 9006 1014 9007 1014 9008 1014 9009 1014 9010 1014 9011

1015 9006 1015 9007 1015 9008 1015 9009 1015 9010 1015 9011

1016 9006 1016 9007 1016 9008 1016 9009 1016 9010 1016 9011

2001 9006 2001 9007 2001 9008 2001 9009 2001 9010 2001 9011

2002 9006 2002 9007 2002 9008 2002 9009 2002 9010 2002 9011

2003 9006 2003 9007 2003 9008 2003 9009 2003 9010 2003 9011

2004 9006 2004 9007 2004 9008 2004 9009 2004 9010 2004 9011

2005 9006 2005 9007 2005 9008 2005 9009 2005 9010 2005 9011

2006 9006 2006 9007 2006 9008 2006 9009 2006 9010 2006 9011

2007 9006 2007 9007 2007 9008 2007 9009 2007 9010 2007 9011

2008 9006 2008 9007 2008 9008 2008 9009 2008 9010 2008 9011

2009 9006 2009 9007 2009 9008 2009 9009 2009 9010 2009 9011

2010 9006 2010 9007 2010 9008 2010 9009 2010 9010 2010 9011

2011 9006 2011 9007 2011 9008 2011 9009 2011 9010 2011 9011

2012 9006 2012 9007 2012 9008 2012 9009 2012 9010 2012 9011

X Y X Y X Υ X Υ X : Υ X : Υ

1001 9012 1001 9013 1001 9014 1001 9015

1002 9012 1002 9013 1002 9014 1002 9015

1003 9012 1003 9013 1003 9014 1003 9015

1004 9012 1004 9013 1004 9014 1004 9015

1005 9012 1005 9013 1005 9014 1005 9015

1006 9012 1006 9013 1006 9014 1006 9015

1007 9012 1007 9013 1007 9014 1007 9015

1008 9012 1008 9013 1008 9014 1008 9015

1009 9012 1009 9013 1009 9014 1009 9015

1010 9012 1010 9013 1010 9014 1010 9015

1011 9012 1011 9013 1011 9014 1011 9015

1012 9012 1012 9013 1012 9014 1012 9015

1013 9012 1013 9013 1013 9014 1013 9015

1014 9012 1014 9013 1014 9014 1014 9015

1015 9012 1015 9013 1015 9014 1015 9015

1016 9012 1016 9013 1016 9014 1016 9015

2001 9012 2001 9013 2001 9014 2001 9015

2002 9012 2002 9013 2002 9014 2002 9015

2003 9012 2003 9013 2003 9014 2003 9015

2004 9012 2004 9013 2004 9014 2004 9015

2005 9012 2005 9013 2005 9014 2005 9015

2006 9012 2006 9013 2006 9014 2006 9015

2007 9012 2007 9013 2007 9014 2007 9015

2008 9012 2008 9013 2008 9014 2008 9015

2009 9012 2009 9013 2009 9014 2009 9015

2010 9012 2010 9013 2010 9014 2010 9015

2011 9012 2011 9013 2011 9014 2011 9015

2012 9012 2012 9013 2012 9014 2012 9015

Table B: Example combinations of a compound X with a compound Y.

X Y X Y X Y X Y X Y X Y

3001 9000 3001 9001 3001 9002 3001 9003 3001 9004 3001 9005

3002 9000 3002 9001 3002 9002 3002 9003 3002 9004 3002 9005

3003 9000 3003 9001 3003 9002 3003 9003 3003 9004 3003 9005

3004 9000 3004 9001 3004 9002 3004 9003 3004 9004 3004 9005

3005 9000 3005 9001 3005 9002 3005 9003 3005 9004 3005 9005

3006 9000 3006 9001 3006 9002 3006 9003 3006 9004 3006 9005

3007 9000 3007 9001 3007 9002 3007 9003 3007 9004 3007 9005

3008 9000 3008 9001 3008 9002 3008 9003 3008 9004 3008 9005

3009 9000 3009 9001 3009 9002 3009 9003 3009 9004 3009 9005

3010 9000 3010 9001 3010 9002 3010 9003 3010 9004 3010 9005

3011 9000 3011 9001 3011 9002 3011 9003 3011 9004 3011 9005

3012 9000 3012 9001 3012 9002 3012 9003 3012 9004 3012 9005

3013 9000 3013 9001 3013 9002 3013 9003 3013 9004 3013 9005

3014 9000 3014 9001 3014 9002 3014 9003 3014 9004 3014 9005

4001 9000 4001 9001 4001 9002 4001 9003 4001 9004 4001 9005

4002 9000 4002 9001 4002 9002 4002 9003 4002 9004 4002 9005

4003 9000 4003 9001 4003 9002 4003 9003 4003 9004 4003 9005

4004 9000 4004 9001 4004 9002 4004 9003 4004 9004 4004 9005

4005 9000 4005 9001 4005 9002 4005 9003 4005 9004 4005 9005

4006 9000 4006 9001 4006 9002 4006 9003 4006 9004 4006 9005

4007 9000 4007 9001 4007 9002 4007 9003 4007 9004 4007 9005

4008 9000 4008 9001 4008 9002 4008 9003 4008 9004 4008 9005

4009 9000 4009 9001 4009 9002 4009 9003 4009 9004 4009 9005

4010 9000 4010 9001 4010 9002 4010 9003 4010 9004 4010 9005

4011 9000 4011 9001 4011 9002 4011 9003 4011 9004 4011 9005

4012 9000 4012 9001 4012 9002 4012 9003 4012 9004 4012 9005

5001 9000 5001 9001 5001 9002 5001 9003 5001 9004 5001 9005

5002 9000 5002 9001 5002 9002 5002 9003 5002 9004 5002 9005

5003 9000 5003 9001 5003 9002 5003 9003 5003 9004 5003 9005

5004 9000 5004 9001 5004 9002 5004 9003 5004 9004 5004 9005

5005 9000 5005 9001 5005 9002 5005 9003 5005 9004 5005 9005

5006 9000 5006 9001 5006 9002 5006 9003 5006 9004 5006 9005

5007 9000 5007 9001 5007 9002 5007 9003 5007 9004 5007 9005

5008 9000 5008 9001 5008 9002 5008 9003 5008 9004 5008 9005

5009 9000 5009 9001 5009 9002 5009 9003 5009 9004 5009 9005

5010 9000 5010 9001 5010 9002 5010 9003 5010 9004 5010 9005

5011 9000 5011 9001 5011 9002 5011 9003 5011 9004 5011 9005

5012 9000 5012 9001 5012 9002 5012 9003 5012 9004 5012 9005 X Y X Y X Υ X Υ X Υ X Υ

3001 9006 3001 9007 3001 9008 3001 9009 3001 9010 3001 9011

3002 9006 3002 9007 3002 9008 3002 9009 3002 9010 3002 9011

3003 9006 3003 9007 3003 9008 3003 9009 3003 9010 3003 9011

3004 9006 3004 9007 3004 9008 3004 9009 3004 9010 3004 9011

3005 9006 3005 9007 3005 9008 3005 9009 3005 9010 3005 9011

3006 9006 3006 9007 3006 9008 3006 9009 3006 9010 3006 9011

3007 9006 3007 9007 3007 9008 3007 9009 3007 9010 3007 9011

3008 9006 3008 9007 3008 9008 3008 9009 3008 9010 3008 9011

3009 9006 3009 9007 3009 9008 3009 9009 3009 9010 3009 9011

3010 9006 3010 9007 3010 9008 3010 9009 3010 9010 3010 9011

3011 9006 3011 9007 3011 9008 3011 9009 3011 9010 3011 9011

3012 9006 3012 9007 3012 9008 3012 9009 3012 9010 3012 9011

3013 9006 3013 9007 3013 9008 3013 9009 3013 9010 3013 9011

3014 9006 3014 9007 3014 9008 3014 9009 3014 9010 3014 9011

4001 9006 4001 9007 4001 9008 4001 9009 4001 9010 4001 9011

4002 9006 4002 9007 4002 9008 4002 9009 4002 9010 4002 9011

4003 9006 4003 9007 4003 9008 4003 9009 4003 9010 4003 9011

4004 9006 4004 9007 4004 9008 4004 9009 4004 9010 4004 9011

4005 9006 4005 9007 4005 9008 4005 9009 4005 9010 4005 9011

4006 9006 4006 9007 4006 9008 4006 9009 4006 9010 4006 9011

4007 9006 4007 9007 4007 9008 4007 9009 4007 9010 4007 9011

4008 9006 4008 9007 4008 9008 4008 9009 4008 9010 4008 9011

4009 9006 4009 9007 4009 9008 4009 9009 4009 9010 4009 9011

4010 9006 4010 9007 4010 9008 4010 9009 4010 9010 4010 9011

4011 9006 4011 9007 4011 9008 4011 9009 4011 9010 4011 9011

4012 9006 4012 9007 4012 9008 4012 9009 4012 9010 4012 9011

5001 9006 5001 9007 5001 9008 5001 9009 5001 9010 5001 9011

5002 9006 5002 9007 5002 9008 5002 9009 5002 9010 5002 9011

5003 9006 5003 9007 5003 9008 5003 9009 5003 9010 5003 9011

5004 9006 5004 9007 5004 9008 5004 9009 5004 9010 5004 9011

5005 9006 5005 9007 5005 9008 5005 9009 5005 9010 5005 9011

5006 9006 5006 9007 5006 9008 5006 9009 5006 9010 5006 9011

5007 9006 5007 9007 5007 9008 5007 9009 5007 9010 5007 9011

5008 9006 5008 9007 5008 9008 5008 9009 5008 9010 5008 9011

5009 9006 5009 9007 5009 9008 5009 9009 5009 9010 5009 9011

5010 9006 5010 9007 5010 9008 5010 9009 5010 9010 5010 9011

5011 9006 5011 9007 5011 9008 5011 9009 5011 9010 5011 9011

5012 9006 5012 9007 5012 9008 5012 9009 5012 9010 5012 9011

X Y X Y X Υ X Υ X : Υ X : Υ

3001 9012 3001 9013 3001 9014 3001 9015

3002 9012 3002 9013 3002 9014 3002 9015

3003 9012 3003 9013 3003 9014 3003 9015

3004 9012 3004 9013 3004 9014 3004 9015

3005 9012 3005 9013 3005 9014 3005 9015

3006 9012 3006 9013 3006 9014 3006 9015

3007 9012 3007 9013 3007 9014 3007 9015

3008 9012 3008 9013 3008 9014 3008 9015

3009 9012 3009 9013 3009 9014 3009 9015

3010 9012 3010 9013 3010 9014 3010 9015

3011 9012 3011 9013 3011 9014 3011 9015

3012 9012 3012 9013 3012 9014 3012 9015

3013 9012 3013 9013 3013 9014 3013 9015

3014 9012 3014 9013 3014 9014 3014 9015

4001 9012 4001 9013 4001 9014 4001 9015

4002 9012 4002 9013 4002 9014 4002 9015

4003 9012 4003 9013 4003 9014 4003 9015

4004 9012 4004 9013 4004 9014 4004 9015

4005 9012 4005 9013 4005 9014 4005 9015

4006 9012 4006 9013 4006 9014 4006 9015

4007 9012 4007 9013 4007 9014 4007 9015

4008 9012 4008 9013 4008 9014 4008 9015

4009 9012 4009 9013 4009 9014 4009 9015

4010 9012 4010 9013 4010 9014 4010 9015

4011 9012 4011 9013 4011 9014 4011 9015

4012 9012 4012 9013 4012 9014 4012 9015

5001 9012 5001 9013 5001 9014 5001 9015

5002 9012 5002 9013 5002 9014 5002 9015

5003 9012 5003 9013 5003 9014 5003 9015

5004 9012 5004 9013 5004 9014 5004 9015

5005 9012 5005 9013 5005 9014 5005 9015

5006 9012 5006 9013 5006 9014 5006 9015

5007 9012 5007 9013 5007 9014 5007 9015

5008 9012 5008 9013 5008 9014 5008 9015

5009 9012 5009 9013 5009 9014 5009 9015

5010 9012 5010 9013 5010 9014 5010 9015

5011 9012 5011 9013 5011 9014 5011 9015

5012 9012 5012 9013 5012 9014 5012 9015

Table C: Example combinations of a compound X with a compound Y.

X Y X Y X Y X Y X Y X Y

6000 9000 6043 9000 6000 9001 6043 9001 6000 9002 6043 9002

6001 9000 6044 9000 6001 9001 6044 9001 6001 9002 6044 9002

6002 9000 6045 9000 6002 9001 6045 9001 6002 9002 6045 9002

6003 9000 6046 9000 6003 9001 6046 9001 6003 9002 6046 9002

6004 9000 6047 9000 6004 9001 6047 9001 6004 9002 6047 9002

6005 9000 6048 9000 6005 9001 6048 9001 6005 9002 6048 9002

6006 9000 6049 9000 6006 9001 6049 9001 6006 9002 6049 9002

6007 9000 6050 9000 6007 9001 6050 9001 6007 9002 6050 9002

6008 9000 6051 9000 6008 9001 6051 9001 6008 9002 6051 9002

6009 9000 6052 9000 6009 9001 6052 9001 6009 9002 6052 9002

6010 9000 6053 9000 6010 9001 6053 9001 6010 9002 6053 9002

6011 9000 6054 9000 6011 9001 6054 9001 6011 9002 6054 9002

6012 9000 6055 9000 6012 9001 6055 9001 6012 9002 6055 9002

6013 9000 6056 9000 6013 9001 6056 9001 6013 9002 6056 9002

6014 9000 6057 9000 6014 9001 6057 9001 6014 9002 6057 9002

6015 9000 6058 9000 6015 9001 6058 9001 6015 9002 6058 9002

6016 9000 6059 9000 6016 9001 6059 9001 6016 9002 6059 9002

6017 9000 6060 9000 6017 9001 6060 9001 6017 9002 6060 9002

6018 9000 6061 9000 6018 9001 6061 9001 6018 9002 6061 9002

6019 9000 6062 9000 6019 9001 6062 9001 6019 9002 6062 9002

6020 9000 6063 9000 6020 9001 6063 9001 6020 9002 6063 9002

6021 9000 6064 9000 6021 9001 6064 9001 6021 9002 6064 9002

6022 9000 6065 9000 6022 9001 6065 9001 6022 9002 6065 9002

6023 9000 6066 9000 6023 9001 6066 9001 6023 9002 6066 9002

6024 9000 6067 9000 6024 9001 6067 9001 6024 9002 6067 9002

6025 9000 6068 9000 6025 9001 6068 9001 6025 9002 6068 9002

6026 9000 6069 9000 6026 9001 6069 9001 6026 9002 6069 9002

6027 9000 6070 9000 6027 9001 6070 9001 6027 9002 6070 9002

6028 9000 6071 9000 6028 9001 6071 9001 6028 9002 6071 9002

6029 9000 6072 9000 6029 9001 6072 9001 6029 9002 6072 9002

6030 9000 6073 9000 6030 9001 6073 9001 6030 9002 6073 9002

6031 9000 6074 9000 6031 9001 6074 9001 6031 9002 6074 9002

6032 9000 6075 9000 6032 9001 6075 9001 6032 9002 6075 9002

6033 9000 6076 9000 6033 9001 6076 9001 6033 9002 6076 9002

6034 9000 6077 9000 6034 9001 6077 9001 6034 9002 6077 9002

6035 9000 6078 9000 6035 9001 6078 9001 6035 9002 6078 9002

6036 9000 6036 9001 6036 9002

6037 9000 6037 9001 6037 9002

6038 9000 6038 9001 6038 9002

6039 9000 6039 9001 6039 9002

6040 9000 6040 9001 6040 9002

6041 9000 6041 9001 6041 9002

6042 9000 6042 9001 6042 9002 X Y X Y X Υ X Υ X Υ X Υ

6000 9003 6043 9003 6000 9004 6043 9004 6000 9005 6043 9005

6001 9003 6044 9003 6001 9004 6044 9004 6001 9005 6044 9005

6002 9003 6045 9003 6002 9004 6045 9004 6002 9005 6045 9005

6003 9003 6046 9003 6003 9004 6046 9004 6003 9005 6046 9005

6004 9003 6047 9003 6004 9004 6047 9004 6004 9005 6047 9005

6005 9003 6048 9003 6005 9004 6048 9004 6005 9005 6048 9005

6006 9003 6049 9003 6006 9004 6049 9004 6006 9005 6049 9005

6007 9003 6050 9003 6007 9004 6050 9004 6007 9005 6050 9005

6008 9003 6051 9003 6008 9004 6051 9004 6008 9005 6051 9005

6009 9003 6052 9003 6009 9004 6052 9004 6009 9005 6052 9005

6010 9003 6053 9003 6010 9004 6053 9004 6010 9005 6053 9005

6011 9003 6054 9003 6011 9004 6054 9004 6011 9005 6054 9005

6012 9003 6055 9003 6012 9004 6055 9004 6012 9005 6055 9005

6013 9003 6056 9003 6013 9004 6056 9004 6013 9005 6056 9005

6014 9003 6057 9003 6014 9004 6057 9004 6014 9005 6057 9005

6015 9003 6058 9003 6015 9004 6058 9004 6015 9005 6058 9005

6016 9003 6059 9003 6016 9004 6059 9004 6016 9005 6059 9005

6017 9003 6060 9003 6017 9004 6060 9004 6017 9005 6060 9005

6018 9003 6061 9003 6018 9004 6061 9004 6018 9005 6061 9005

6019 9003 6062 9003 6019 9004 6062 9004 6019 9005 6062 9005

6020 9003 6063 9003 6020 9004 6063 9004 6020 9005 6063 9005

6021 9003 6064 9003 6021 9004 6064 9004 6021 9005 6064 9005

6022 9003 6065 9003 6022 9004 6065 9004 6022 9005 6065 9005

6023 9003 6066 9003 6023 9004 6066 9004 6023 9005 6066 9005

6024 9003 6067 9003 6024 9004 6067 9004 6024 9005 6067 9005

6025 9003 6068 9003 6025 9004 6068 9004 6025 9005 6068 9005

6026 9003 6069 9003 6026 9004 6069 9004 6026 9005 6069 9005

6027 9003 6070 9003 6027 9004 6070 9004 6027 9005 6070 9005

6028 9003 6071 9003 6028 9004 6071 9004 6028 9005 6071 9005

6029 9003 6072 9003 6029 9004 6072 9004 6029 9005 6072 9005

6030 9003 6073 9003 6030 9004 6073 9004 6030 9005 6073 9005

6031 9003 6074 9003 6031 9004 6074 9004 6031 9005 6074 9005

6032 9003 6075 9003 6032 9004 6075 9004 6032 9005 6075 9005

6033 9003 6076 9003 6033 9004 6076 9004 6033 9005 6076 9005

6034 9003 6077 9003 6034 9004 6077 9004 6034 9005 6077 9005

6035 9003 6078 9003 6035 9004 6078 9004 6035 9005 6078 9005

6036 9003 6036 9004 6036 9005

6037 9003 6037 9004 6037 9005

6038 9003 6038 9004 6038 9005

6039 9003 6039 9004 6039 9005

6040 9003 6040 9004 6040 9005

6041 9003 6041 9004 6041 9005

6042 9003 6042 9004 6042 9005 -89-

8006 ΖΡ09 .1006 ζΐ709 9006 ζΐ709

8006 \Ρ09 .1006 11709 9006 \Ρ09

8006 0W9 .1006 01709 9006 0Μ)9

8006 6£09 .1006 6ε09 9006 6ε09

8006 8£09 .1006 8ε09 9006 8ε09

8006 ζΐεο9 .1006 ζΐεο9 9006 ζΐεο9

8006 9£09 .1006 9ε09 9006 9ε09

8006 8.109 8006 ££09 L006 8.109 .1006 ££09 9006 8.109 9006 ££09

8006 LLQ9 8006 Ρ£09 LQQ6 LLQ9 .1006 Ρ£09 9006 LLQ9 9006 Ρ£09

8006 9LQ9 8006 εεο9 LQQ6 9LQ9 .1006 εεο9 9006 9LQ9 9006 εεο9

8006 SL09 8006 Ζ£09 LQQ6 SL09 .1006 Ζ£09 9006 £Ζ109 9006 Ζ£09

8006 PL09 8006 ι εο9 Α006 PL09 .1006 ι εο9 9006 PL09 9006 ι εο9

8006 £L09 8006 οεο9 LQQ6 £LQ9 .1006 οεο9 9006 £L09 9006 οεο9

8006 ZLQ9 8006 6^09 LQQ6 ZLQ9 .1006 6£09 9006 ZLQ9 9006 6£09

8006 \L09 8006 8^09 LQQ6 \LQ9 .1006 8£09 9006 \LQ9 9006 8£09

8006 0L09 8006 LZ09 LQQ6 0.109 .1006 LZ09 9006 0.109 9006 LZ09

8006 6909 8006 9^09 Α006 6909 .1006 9£09 9006 6909 9006 9£09

8006 8909 8006 SZ09 LQQ6 8909 .1006 ££09 9006 8909 9006 ££09

8006 Z1909 8006

8006 9909 8006 £Ζ09 LQQ6 9909 .1006 £Ζ09 9006 9909 9006 £Ζ09

8006 £909 8006 ΖΖ09 LQQ6 £909 .1006 ££09 9006 £909 9006 ££09

8006 t-909 8006 \Ζ09 Α006 17909 .1006 ΐ £09 9006 17909 9006 ΐ £09

8006 £909 8006 0Ζ09 LQQ6 ε909 .1006 0£09 9006 ε909 9006 0£09

8006 £909 8006 6109 LQQ6 £909 .1006 6109 9006 £909 9006 6109

8006 1909 8006 8109 LQQ6 1909 .1006 8109 9006 1909 9006 8109

8006 0909 8006 L\09 LQQ6 0909 .1006 /.Ϊ09 9006 0909 9006 /.Ϊ09

8006 6S09 8006 9109 Α006 6S09 .1006 9109 9006 6£09 9006 9109

8006 8S09 8006 ξ\09 LQQ6 8 £09 .1006 £109 9006 8509 9006 £109

8006 Z.S09 8006 Ρ\09 LQQ6 L£09 .1006 17109 9006 zl£09 9006 17109

8006 9S09 8006 εΐ09 LQQ6 9£09 .1006 εΐ09 9006 9£09 9006 εΐ09

8006 ££09 8006 £109 LQQ6 SS09 .1006 £109 9006 ££09 9006 £109

8006 PS09 8006 1109 Α006 P£09 .1006 1 109 9006 P£09 9006 1 109

8006 ££09 8006 0109 LQQ6 ££09 .1006 0109 9006 ££09 9006 0109

8006 ZS09 8006 6009 LQQ6 ££09 .1006 6009 9006 ££09 9006 6009

8006 \£09 8006 8009 LQQ6 ΐ £09 .1006 8009 9006 ΐ £09 9006 8009

8006 0S09 8006 LQQ9 LQQ6 0£09 .1006 .1009 9006 0£09 9006 .1009

8006 61709 8006 9009 Α006 61709 .1006 9009 9006 6W9 9006 9009

8006 81709 8006 £009 LQQ6 81709 .1006 £009 9006 8W9 9006 £009

8006 LPQ9 8006 17009 LQQ6 LPQ9 .1006 17009 9006 LPQ9 9006 17009

8006 9W)9 8006 εοο9 LQQ6 9Ρ09 .1006 εοο9 9006 9Ρ09 9006 εοο9

8006 £P09 8006 £009 LQQ6 £Ρ09 .1006 £009 9006 £Ρ09 9006 £009

8006 171 09 8006 1009 Α006 171 09 .1006 1009 9006 Ι7ΐ709 9006 1009

8006 εΐ 09 8006 0009 LQQ6 εΐ709 .1006 0009 9006 εΐ709 9006 0009

A X A X A X A X A X A X

_.Z_.9_.0/£T0ZSil/I3d 86^00Τ/*Ί0ε OAV X Y X Y X Υ X Υ X Υ X Υ

6000 9009 6043 9009 6000 9010 6043 9010 6000 9011 6043 9011

6001 9009 6044 9009 6001 9010 6044 9010 6001 9011 6044 9011

6002 9009 6045 9009 6002 9010 6045 9010 6002 9011 6045 9011

6003 9009 6046 9009 6003 9010 6046 9010 6003 9011 6046 9011

6004 9009 6047 9009 6004 9010 6047 9010 6004 9011 6047 9011

6005 9009 6048 9009 6005 9010 6048 9010 6005 9011 6048 9011

6006 9009 6049 9009 6006 9010 6049 9010 6006 9011 6049 9011

6007 9009 6050 9009 6007 9010 6050 9010 6007 9011 6050 9011

6008 9009 6051 9009 6008 9010 6051 9010 6008 9011 6051 9011

6009 9009 6052 9009 6009 9010 6052 9010 6009 9011 6052 9011

6010 9009 6053 9009 6010 9010 6053 9010 6010 9011 6053 9011

6011 9009 6054 9009 6011 9010 6054 9010 6011 9011 6054 9011

6012 9009 6055 9009 6012 9010 6055 9010 6012 9011 6055 9011

6013 9009 6056 9009 6013 9010 6056 9010 6013 9011 6056 9011

6014 9009 6057 9009 6014 9010 6057 9010 6014 9011 6057 9011

6015 9009 6058 9009 6015 9010 6058 9010 6015 9011 6058 9011

6016 9009 6059 9009 6016 9010 6059 9010 6016 9011 6059 9011

6017 9009 6060 9009 6017 9010 6060 9010 6017 9011 6060 9011

6018 9009 6061 9009 6018 9010 6061 9010 6018 9011 6061 9011

6019 9009 6062 9009 6019 9010 6062 9010 6019 9011 6062 9011

6020 9009 6063 9009 6020 9010 6063 9010 6020 9011 6063 9011

6021 9009 6064 9009 6021 9010 6064 9010 6021 9011 6064 9011

6022 9009 6065 9009 6022 9010 6065 9010 6022 9011 6065 9011

6023 9009 6066 9009 6023 9010 6066 9010 6023 9011 6066 9011

6024 9009 6067 9009 6024 9010 6067 9010 6024 9011 6067 9011

6025 9009 6068 9009 6025 9010 6068 9010 6025 9011 6068 9011

6026 9009 6069 9009 6026 9010 6069 9010 6026 9011 6069 9011

6027 9009 6070 9009 6027 9010 6070 9010 6027 9011 6070 9011

6028 9009 6071 9009 6028 9010 6071 9010 6028 9011 6071 9011

6029 9009 6072 9009 6029 9010 6072 9010 6029 9011 6072 9011

6030 9009 6073 9009 6030 9010 6073 9010 6030 9011 6073 9011

6031 9009 6074 9009 6031 9010 6074 9010 6031 9011 6074 9011

6032 9009 6075 9009 6032 9010 6075 9010 6032 9011 6075 9011

6033 9009 6076 9009 6033 9010 6076 9010 6033 9011 6076 9011

6034 9009 6077 9009 6034 9010 6077 9010 6034 9011 6077 9011

6035 9009 6078 9009 6035 9010 6078 9010 6035 9011 6078 9011

6036 9009 6036 9010 6036 9011

6037 9009 6037 9010 6037 9011

6038 9009 6038 9010 6038 9011

6039 9009 6039 9010 6039 9011

6040 9009 6040 9010 6040 9011

6041 9009 6041 9010 6041 9011

6042 9009 6042 9010 6042 9011 X Y X Y X Υ X Υ X Υ X Υ

6000 9012 6043 9012 6000 9013 6043 9013 6000 9014 6043 9014

6001 9012 6044 9012 6001 9013 6044 9013 6001 9014 6044 9014

6002 9012 6045 9012 6002 9013 6045 9013 6002 9014 6045 9014

6003 9012 6046 9012 6003 9013 6046 9013 6003 9014 6046 9014

6004 9012 6047 9012 6004 9013 6047 9013 6004 9014 6047 9014

6005 9012 6048 9012 6005 9013 6048 9013 6005 9014 6048 9014

6006 9012 6049 9012 6006 9013 6049 9013 6006 9014 6049 9014

6007 9012 6050 9012 6007 9013 6050 9013 6007 9014 6050 9014

6008 9012 6051 9012 6008 9013 6051 9013 6008 9014 6051 9014

6009 9012 6052 9012 6009 9013 6052 9013 6009 9014 6052 9014

6010 9012 6053 9012 6010 9013 6053 9013 6010 9014 6053 9014

6011 9012 6054 9012 6011 9013 6054 9013 6011 9014 6054 9014

6012 9012 6055 9012 6012 9013 6055 9013 6012 9014 6055 9014

6013 9012 6056 9012 6013 9013 6056 9013 6013 9014 6056 9014

6014 9012 6057 9012 6014 9013 6057 9013 6014 9014 6057 9014

6015 9012 6058 9012 6015 9013 6058 9013 6015 9014 6058 9014

6016 9012 6059 9012 6016 9013 6059 9013 6016 9014 6059 9014

6017 9012 6060 9012 6017 9013 6060 9013 6017 9014 6060 9014

6018 9012 6061 9012 6018 9013 6061 9013 6018 9014 6061 9014

6019 9012 6062 9012 6019 9013 6062 9013 6019 9014 6062 9014

6020 9012 6063 9012 6020 9013 6063 9013 6020 9014 6063 9014

6021 9012 6064 9012 6021 9013 6064 9013 6021 9014 6064 9014

6022 9012 6065 9012 6022 9013 6065 9013 6022 9014 6065 9014

6023 9012 6066 9012 6023 9013 6066 9013 6023 9014 6066 9014

6024 9012 6067 9012 6024 9013 6067 9013 6024 9014 6067 9014

6025 9012 6068 9012 6025 9013 6068 9013 6025 9014 6068 9014

6026 9012 6069 9012 6026 9013 6069 9013 6026 9014 6069 9014

6027 9012 6070 9012 6027 9013 6070 9013 6027 9014 6070 9014

6028 9012 6071 9012 6028 9013 6071 9013 6028 9014 6071 9014

6029 9012 6072 9012 6029 9013 6072 9013 6029 9014 6072 9014

6030 9012 6073 9012 6030 9013 6073 9013 6030 9014 6073 9014

6031 9012 6074 9012 6031 9013 6074 9013 6031 9014 6074 9014

6032 9012 6075 9012 6032 9013 6075 9013 6032 9014 6075 9014

6033 9012 6076 9012 6033 9013 6076 9013 6033 9014 6076 9014

6034 9012 6077 9012 6034 9013 6077 9013 6034 9014 6077 9014

6035 9012 6078 9012 6035 9013 6078 9013 6035 9014 6078 9014

6036 9012 6036 9013 6036 9014

6037 9012 6037 9013 6037 9014

6038 9012 6038 9013 6038 9014

6039 9012 6039 9013 6039 9014

6040 9012 6040 9013 6040 9014

6041 9012 6041 9013 6041 9014

6042 9012 6042 9013 6042 9014 X : Y X : Y X : Υ X : Υ X : Υ X : Υ

6000 9015 6043 9015

6001 9015 6044 9015

6002 9015 6045 9015

6003 9015 6046 9015

6004 9015 6047 9015

6005 9015 6048 9015

6006 9015 6049 9015

6007 9015 6050 9015

6008 9015 6051 9015

6009 9015 6052 9015

6010 9015 6053 9015

6011 9015 6054 9015

6012 9015 6055 9015

6013 9015 6056 9015

6014 9015 6057 9015

6015 9015 6058 9015

6016 9015 6059 9015

6017 9015 6060 9015

6018 9015 6061 9015

6019 9015 6062 9015

6020 9015 6063 9015

6021 9015 6064 9015

6022 9015 6065 9015

6023 9015 6066 9015

6024 9015 6067 9015

6025 9015 6068 9015

6026 9015 6069 9015

6027 9015 6070 9015

6028 9015 6071 9015

6029 9015 6072 9015

6030 9015 6073 9015

6031 9015 6074 9015

6032 9015 6075 9015

6033 9015 6076 9015

6034 9015 6077 9015

6035 9015 6078 9015

6036 9015

6037 9015

6038 9015

6039 9015

6040 9015

6041 9015

6042 9015 Table D: Example combinations of a compound X with a compound Y.

X Y X Y X Y X Y X Y X Y

9000 7000 9001 7000 9002 7000 9003 7000 9004 7000 9005 7000

9000 7001 9001 7001 9002 7001 9003 7001 9004 7001 9005 7001

9000 7002 9001 7002 9002 7002 9003 7002 9004 7002 9005 7002

9000 7003 9001 7003 9002 7003 9003 7003 9004 7003 9005 7003

9000 7004 9001 7004 9002 7004 9003 7004 9004 7004 9005 7004

9000 7005 9001 7005 9002 7005 9003 7005 9004 7005 9005 7005

9000 7006 9001 7006 9002 7006 9003 7006 9004 7006 9005 7006

9000 7007 9001 7007 9002 7007 9003 7007 9004 7007 9005 7007

9000 7008 9001 7008 9002 7008 9003 7008 9004 7008 9005 7008

9000 7009 9001 7009 9002 7009 9003 7009 9004 7009 9005 7009

9000 7010 9001 7010 9002 7010 9003 7010 9004 7010 9005 7010

9000 7011 9001 7011 9002 7011 9003 7011 9004 7011 9005 7011

9000 7012 9001 7012 9002 7012 9003 7012 9004 7012 9005 7012

9000 7013 9001 7013 9002 7013 9003 7013 9004 7013 9005 7013

9000 7014 9001 7014 9002 7014 9003 7014 9004 7014 9005 7014

9000 7015 9001 7015 9002 7015 9003 7015 9004 7015 9005 7015

9000 7016 9001 7016 9002 7016 9003 7016 9004 7016 9005 7016

9000 7017 9001 7017 9002 7017 9003 7017 9004 7017 9005 7017

9000 7018 9001 7018 9002 7018 9003 7018 9004 7018 9005 7018

9000 7019 9001 7019 9002 7019 9003 7019 9004 7019 9005 7019

9000 7020 9001 7020 9002 7020 9003 7020 9004 7020 9005 7020

9000 7021 9001 7021 9002 7021 9003 7021 9004 7021 9005 7021

9000 7022 9001 7022 9002 7022 9003 7022 9004 7022 9005 7022

9000 7023 9001 7023 9002 7023 9003 7023 9004 7023 9005 7023

9000 7024 9001 7024 9002 7024 9003 7024 9004 7024 9005 7024

9000 7025 9001 7025 9002 7025 9003 7025 9004 7025 9005 7025

9000 7026 9001 7026 9002 7026 9003 7026 9004 7026 9005 7026

9000 7027 9001 7027 9002 7027 9003 7027 9004 7027 9005 7027

X Y X Y X Υ X Υ X Υ X Υ

9006 7000 9007 7000 9008 7000 9009 7000 9010 7000 9011 7000

9006 7001 9007 7001 9008 7001 9009 7001 9010 7001 9011 7001

9006 7002 9007 7002 9008 7002 9009 7002 9010 7002 9011 7002

9006 7003 9007 7003 9008 7003 9009 7003 9010 7003 9011 7003

9006 7004 9007 7004 9008 7004 9009 7004 9010 7004 9011 7004

9006 7005 9007 7005 9008 7005 9009 7005 9010 7005 9011 7005

9006 7006 9007 7006 9008 7006 9009 7006 9010 7006 9011 7006

9006 7007 9007 7007 9008 7007 9009 7007 9010 7007 9011 7007

9006 7008 9007 7008 9008 7008 9009 7008 9010 7008 9011 7008

9006 7009 9007 7009 9008 7009 9009 7009 9010 7009 9011 7009

9006 7010 9007 7010 9008 7010 9009 7010 9010 7010 9011 7010

9006 7011 9007 7011 9008 7011 9009 7011 9010 7011 9011 7011

9006 7012 9007 7012 9008 7012 9009 7012 9010 7012 9011 7012

9006 7013 9007 7013 9008 7013 9009 7013 9010 7013 9011 7013

9006 7014 9007 7014 9008 7014 9009 7014 9010 7014 9011 7014

9006 7015 9007 7015 9008 7015 9009 7015 9010 7015 9011 7015

9006 7016 9007 7016 9008 7016 9009 7016 9010 7016 9011 7016

9006 7017 9007 7017 9008 7017 9009 7017 9010 7017 9011 7017

9006 7018 9007 7018 9008 7018 9009 7018 9010 7018 9011 7018

9006 7019 9007 7019 9008 7019 9009 7019 9010 7019 9011 7019

9006 7020 9007 7020 9008 7020 9009 7020 9010 7020 9011 7020

9006 7021 9007 7021 9008 7021 9009 7021 9010 7021 9011 7021

9006 7022 9007 7022 9008 7022 9009 7022 9010 7022 9011 7022

9006 7023 9007 7023 9008 7023 9009 7023 9010 7023 9011 7023

9006 7024 9007 7024 9008 7024 9009 7024 9010 7024 9011 7024

9006 7025 9007 7025 9008 7025 9009 7025 9010 7025 9011 7025

9006 7026 9007 7026 9008 7026 9009 7026 9010 7026 9011 7026

9006 7027 9007 7027 9008 7027 9009 7027 9010 7027 9011 7027

X Y X Y X Υ X Υ X : Υ X : Υ

9012 7000 9013 7000 9014 7000 9015 7000

9012 7001 9013 7001 9014 7001 9015 7001

9012 7002 9013 7002 9014 7002 9015 7002

9012 7003 9013 7003 9014 7003 9015 7003

9012 7004 9013 7004 9014 7004 9015 7004

9012 7005 9013 7005 9014 7005 9015 7005

9012 7006 9013 7006 9014 7006 9015 7006

9012 7007 9013 7007 9014 7007 9015 7007

9012 7008 9013 7008 9014 7008 9015 7008

9012 7009 9013 7009 9014 7009 9015 7009

9012 7010 9013 7010 9014 7010 9015 7010

9012 7011 9013 7011 9014 7011 9015 7011

9012 7012 9013 7012 9014 7012 9015 7012

9012 7013 9013 7013 9014 7013 9015 7013

9012 7014 9013 7014 9014 7014 9015 7014

9012 7015 9013 7015 9014 7015 9015 7015

9012 7016 9013 7016 9014 7016 9015 7016

9012 7017 9013 7017 9014 7017 9015 7017

9012 7018 9013 7018 9014 7018 9015 7018

9012 7019 9013 7019 9014 7019 9015 7019

9012 7020 9013 7020 9014 7020 9015 7020

9012 7021 9013 7021 9014 7021 9015 7021

9012 7022 9013 7022 9014 7022 9015 7022

9012 7023 9013 7023 9014 7023 9015 7023

9012 7024 9013 7024 9014 7024 9015 7024

9012 7025 9013 7025 9014 7025 9015 7025

9012 7026 9013 7026 9014 7026 9015 7026

9012 7027 9013 7027 9014 7027 9015 7027

Table Ε: Example combinations of a compound X with a compound Y.

X Y X Y X Y X Y X Y X Y

8000 9000 8000 9001 8000 9002 8000 9003 8000 9004 8000 9005

8001 9000 8001 9001 8001 9002 8001 9003 8001 9004 8001 9005

8002 9000 8002 9001 8002 9002 8002 9003 8002 9004 8002 9005

8003 9000 8003 9001 8003 9002 8003 9003 8003 9004 8003 9005

8004 9000 8004 9001 8004 9002 8004 9003 8004 9004 8004 9005

8005 9000 8005 9001 8005 9002 8005 9003 8005 9004 8005 9005

8006 9000 8006 9001 8006 9002 8006 9003 8006 9004 8006 9005

8007 9000 8007 9001 8007 9002 8007 9003 8007 9004 8007 9005

8008 9000 8008 9001 8008 9002 8008 9003 8008 9004 8008 9005

8009 9000 8009 9001 8009 9002 8009 9003 8009 9004 8009 9005

8010 9000 8010 9001 8010 9002 8010 9003 8010 9004 8010 9005

8011 9000 8011 9001 8011 9002 8011 9003 8011 9004 8011 9005

8012 9000 8012 9001 8012 9002 8012 9003 8012 9004 8012 9005

8013 9000 8013 9001 8013 9002 8013 9003 8013 9004 8013 9005

8014 9000 8014 9001 8014 9002 8014 9003 8014 9004 8014 9005

8015 9000 8015 9001 8015 9002 8015 9003 8015 9004 8015 9005

8016 9000 8016 9001 8016 9002 8016 : 9003 8016 : 9004 8016 : 9005 X Y X Y X Υ X Υ X Υ X Υ

8000 9006 8000 9007 8000 9008 8000 9009 8000 9010 8000 901 1

8001 9006 8001 9007 8001 9008 8001 9009 8001 9010 8001 901 1

8002 9006 8002 9007 8002 9008 8002 9009 8002 9010 8002 901 1

8003 9006 8003 9007 8003 9008 8003 9009 8003 9010 8003 901 1

8004 9006 8004 9007 8004 9008 8004 9009 8004 9010 8004 901 1

8005 9006 8005 9007 8005 9008 8005 9009 8005 9010 8005 901 1

8006 9006 8006 9007 8006 9008 8006 9009 8006 9010 8006 901 1

8007 9006 8007 9007 8007 9008 8007 9009 8007 9010 8007 901 1

8008 9006 8008 9007 8008 9008 8008 9009 8008 9010 8008 901 1

8009 9006 8009 9007 8009 9008 8009 9009 8009 9010 8009 901 1

8010 9006 8010 9007 8010 9008 8010 9009 8010 9010 8010 901 1

8011 9006 801 1 9007 801 1 9008 801 1 9009 801 1 9010 8011 901 1

8012 9006 8012 9007 8012 9008 8012 9009 8012 9010 8012 901 1

8013 9006 8013 9007 8013 9008 8013 9009 8013 9010 8013 901 1

8014 9006 8014 9007 8014 9008 8014 9009 8014 9010 8014 901 1

8015 9006 8015 9007 8015 9008 8015 9009 8015 9010 8015 901 1

8016 9006 8016 9007 8016 9008 8016 9009 8016 9010 8016 901 1

8000 9012 8000 9013 8000 9014 8000 9015

8001 9012 8001 9013 8001 9014 8001 9015

8002 9012 8002 9013 8002 9014 8002 9015

8003 9012 8003 9013 8003 9014 8003 9015

8004 9012 8004 9013 8004 9014 8004 9015

8005 9012 8005 9013 8005 9014 8005 9015

8006 9012 8006 9013 8006 9014 8006 9015

8007 9012 8007 9013 8007 9014 8007 9015

8008 9012 8008 9013 8008 9014 8008 9015 - - - -

8009 9012 8009 9013 8009 9014 8009 9015

8010 9012 8010 9013 8010 9014 8010 9015

8011 9012 801 1 9013 801 1 9014 801 1 9015

8012 9012 8012 9013 8012 9014 8012 9015

8013 9012 8013 9013 8013 9014 8013 9015

8014 9012 8014 9013 8014 9014 8014 9015

8015 9012 8015 9013 8015 9014 8015 9015

8016 9012 8016 9013 8016 9014 8016 9015

EXAMPLES

[0186] Additional embodiments are disclosed in further detail in the following examples, which are not in any way intended to limit the scope of the claims. EXAMPLE 1

(2R,3S,4R,5R)-2-(2-amino-6-ethoxy-9H-purin-9-yl)-4-nuoro-5-( hvdroxymethyl)-3- -3-ol (1)

[0187] Preparation of (32-2): To a stirred solution of 1-1 (5.0 g, 19.53 mmol) in anhydrous MeCN was added IBX (7.66 g, 27.34 mmol), and the mixture was heated to 80 °C for 12 h. The mixture was cooled to room temperature (R.T.) and filtered. The filtrate was concentrated to dryness to give the ketone (4.87 g, 98%) as a colorless oil. To a solution of the ketone (4.87 g, 19.33 mmol) in anhydrous THF was added methyl magnesium bromide (19.53 mL, 58.59 mmol) dropwise at -78 °C under N ₂ . The mixture was warmed to R.T. for 12 h. The reaction was quenched with a saturated ammonium chloride solution, extracted with ethyl acetate (EA) and concentrated to give a residue, which was purified on a silica gel column (2- 10% EA in PE) to give 1-2 (4.37 g, 83%) as colorless oil.

[0188] Preparation of (32-3): To a solution of 1-2 (4.37 g, 16.19 mmol) in anhydrous dichloromethane, DMAP (3.95 g, 32.38 mmol), TEA (4.91 g, 48.56 mmol) in ice water bath was added BzCl (6.80 g, 48.56 mmol). The mixture was stirred at R.T. for 12 h. The reaction was quenched with a saturated sodium hydrogen carbonate solution and extracted with EA. The organic phase was concentrated to dryness and purified on a silica gel column (2-20% EA in PE) to give 1-3 (5.3 g, 87%) as a colorless oil.

[0189] Preparation of (32-4): To a solution of 1-3 (2.0 g, 5.33 mmol) and Ac ₂ 0 (4.91 g, 48.13 mmol) in acetic acid (50 mL) was added concentrated H2SO4 (0.6 g, 6.01 mmol) at 0 °C. The mixture was stirred at R.T. for 12 h. The mixture was then poured into ice water and extracted with EA. The organic phase was concentrated to dryness, and the residue was purified on a silica gel column (2-30% EA in PE) to give 1-4 (1.5 g, 81%) as a colorless oil.

[0190] Preparation of (32-5): To a stirred solution of 6-chloroguanine (560 mg, 3.31 mmol) and 1-4 (1.1 1 g, 2.76 mmol) in anhydrous MeCN (5 mL) under N2 was added 1,8- diazobicyclo[5.4.0] undec-7-ene (1.27 g, 8.28 mmol) at 0 °C. The mixture was stirred at R.T. for 0.5 h. TMSOTf (2.45 g, 11.04 mmol) was added at 0 °C. The mixture was heated to 60°C for 4 h and then concentrated to dryness. The residue was partitioned between EA and saturated sodium hydrogen carbonate. The organic phase was separated and concentrated to dryness. The residue was purified on a silica gel column (2-60% EA in PE) to give 1-5 (800 mg, 70%) as a white foam solid.

[0191] Preparation of (1): To a solution of 1-6 (500 mg, 0.68 mmol) in anhydrous ethanol was added sodium ethoxide (0.64 mL, 2.04 mmol) at R.T. The mixture was stirred at R.T. for 16 h. The reaction was quenched by acetic acid to pH = 7. The solvent was removed under reduce pressure. The residue was re-dissolved in EA, and washed with water and brine. The organic phase was dried and concentrated to dryness. The residue was purified on a silica gel column (1-3% DCM in MeOH) to give 1 (400 mg, 98%) as a white foam. ESI-MS: m/z 327.8 [M+H] ⁺ .

EXAMPLE 2

i2SVneopentyl 2-rrrrr2R.3R.4S.5RV5-r2-amino-6-ethoxy-lH-purin-9r6HVylV3-nu oro-4- hvdroxy-4-methyltetrahvdrofuran-2-yl)methoxy)(2- chlorophenoxy)phosphoryl)amino)propanoate (2)

[0192] Preparation of (2-2): To a stirred solution of 2-1 (2.00 g, 13.16 mmol) and 2-chlorophenol (1.68 g, 13.16 mmol) in anhydrous DCM (100 mL) was added a solution of TEA (1.33 g, 13.16 mmol) in DCM (20 mL) dropwise at -78°C. After the addition, the mixture was gradually warmed to R.T. and stirred for 2 h. The solution was re-cooled to -78 °C and neopentyl 2-aminopropanoate hydrogen chloride (3.51 g, 13.16 mmol) was added, followed by TEA (2.66 g, 26.32 mmol) dropwise at -78 °C. The mixture was gradually warmed to R.T. and stirred at R.T. for 2 h. The solvent was removed, and the residue was dissolved in methyl-butyl ether. The precipitate was filtered off, and the filtrate was concentrated to dryness. The residue was purified on a silica gel column (pure anhydrous DCM) to give 2-2 (1.86 g, 32.18%) as a colorless oil.

[0193] Preparation of (2): To a stirred solution of 1 (100 mg, 0.31 mmol) in anhydrous THF (10 mL) was added ?-BuMgCl (1.53 mL, 1M in THF) dropwise at -78 °C. The mixture was stirred at R.T. for 30 mins and re-cooled to -78 °C. To the above mixture was added 2-2 (561 mg, 1.53 mmol) dropwise. The mixture was stirred at R.T. for 2 h. The reaction was quenched with water and extracted with EA. The organic layer was dried over anhydrous a2S0 ₄ and concentrated to dryness. The residue was purified on a silica gel column (1-8% DCM in MeOH) to give the crude product, which was further purified by RP HPLC (water and MeCN system) to give 2 (19.83 mg, 10%) as a white solid. ESI-LCMS: m/z 659.3 [M+H] ⁺ .

EXAMPLE 3

r2SVcvclohexyl 2-rrrrr2R.3R.4S.5RV5-r2-amino-6-ethoxy-lH-purin-9r6HVylV3-nu oro-4- hvdroxy-4-methyltetrahvdrofuran-2-yl)methoxy)(3-chloro-4- fluorophenoxy)phosphoryl)amino)propanoate (3)

[0194] Preparation of (3-1): To a stirred solution of phosphoryl trichloride (2.00 g, 13.16 mmol) and phenol (1.92 g, 13.16 mmol) in anhydrous DCM (100 mL) was added a solution of TEA (1.33 g, 13.16 mmol) in DCM (20 mL) dropwise at -78 °C. After addition, the mixture was gradually warmed to R.T. and stirred for 2 h. The solution was re-cooled to -78 °C and the amine (2.72 g, 13.16 mmol) was added, followed by TEA (2.66 g, 26.32 mmol) dropwise at -78 °C. The mixture was gradually warmed to R.T. and stirred for 2 h. The solvent was removed, and the residue was dissolved in methyl-butyl ether. The precipitate was filtered off, and the filtrate was concentrated. The residue was purified on a silica gel column (pure anhydrous DCM) to give 3-1 (1.90 g, 36.39%) as a colorless oil.

[0195] Preparation of (3): To a stirred solution of 1 (181 mg, 0.55 mmol) in anhydrous THF (10 mL) was added /-BuMgCl (2.77 mL, 1M in THF) dropwise at -78 °C. The mixture was stirred at R.T. for 30 mins and re-cooled to -78 °C. To the mixture was added 3-1 (1.01 g, 2.77 mmol) dropwise. The mixture was stirred at R.T. for 12 h. The reaction was quenched with water and extracted with EA. The organic layer was dried over anhydrous a2S0 ₄ and concentrated to dryness. The residue was purified on a silica gel column (1-8% DCM in MeOH) to give the crude product, which was further purified by RP HPLC (water and MeCN system) to give 3 (76.81 mg, 20%) as a white solid. ESI-LCMS: m/z 689.3 [M+H] ⁺ . EXAMPLE 4

(2S)-neopentyl 2-( ((2R,3R,4S,5RV5-(2-amino-6-ethoxy-lH-purin-9(6H)-vn-3-nuoro- 4- hvdroxy-4-methyltetrahvdrofuran-2-yl)methoxy)(phenoxy)phosph oryl)amino)propanoate

[0196] Preparation of (4-2): To a stirred solution of 4-1 (3.20 g, 15.38 mmol) and amine (3.0 g, 15.38 mmol) in anhydrous DCM (100 mL) was added a solution of TEA (30.76 g, 30.76 mmol) in DCM (20 mL) dropwise at -78 °C. After addition, the mixture was gradually warmed to R.T. and stirred for 2 h. The solvent was removed, and the residue was dissolved in methyl-butyl ether. The precipitate was filtered off, and the filtrate was concentrated. The residue was purified on a silica gel column (pure anhydrous DCM) to give 4-2 (2.0 g, 39%) as a colorless oil.

[0197] Preparation of (4): To a stirred solution of 1 (83 mg, 0.25 mmol) in anhydrous THF (10 mL) was added a solution of ?-BuMgCl (1.27 mL, 1M in THF) dropwise at - 78 °C. The mixture was stirred at R.T. for 30 mins and then re-cooled to -78 °C. A solution of 4-2 (423 mg, 1.27 mmol) was added dropwise, and the mixture was stirred at R.T. for 12 h. The reaction was quenched with water and extracted with EA. The organic layer was dried over Na ₂ S0 ₄ and concentrated. The residue was purified on a silica gel column to give the crude product, which was further purified by RP HPLC (water and MeCN system) to give 4 (80 mg, 51%) as a white solid. ESI-LCMS: m/z 625.1 [M+H] ⁺ .

EXAMPLE 5

(2S)-cvclohexyl 2-(( (2R,3R,4S,5R)-5-(2-amino-6-ethoxy-lH-purin-9(6H)-yl)-3-nuoro -4- hvdroxy-4-methyltetrahvdrofuran-2-yl)methoxy)(phenoxy)phosph oryl)amino)propanoate

£5}

[0198] Preparation of (5-1): To a stirred solution of 4-1 (2.00 g, 9.57 mmol) and amine (1.98 g, 9.57 mmol) in anhydrous DCM (100 mL) was added a solution of TEA (1.93 g, 19.14 mmol) in DCM (20 mL) dropwise at -78 °C. After addition, the mixture was gradually warmed to R.T. and stirred for 2 h. The solvent was removed, and the residue was dissolved in methyl-butyl ether. The precipitate was filtered off, and the filtrate was concentrated. The residue was purified on a silica gel column (pure anhydrous DCM) to give 5-1 (700 mg, 21%) as a colorless oil.

[0199] Preparation of (5): To a stirred solution of 1 (70 mg, 0.21 mmol) in anhydrous THF (1.5 mL) was added a solution of ?-BuMgCl (1.07 mL, 1M in THF) dropwise at -78 °C. The mixture was stirred at R.T. for 30 mins and then re-cooled to -78 °C. A solution of 5-1 (369 mg, 1.07 mmol) was added dropwise. The mixture was stirred at R.T. for 2 h. The reaction was quenched with water and extracted with EA. The organic layer was dried over Na ₂ S0 ₄ and concentrated. The residue was purified on a silica gel column to give the crude product, which was further purified by RP HPLC (water and MeCN system) to give 5 (50 mg, 38%) as a white solid. ESI-LCMS: m/z 637.01 [M+H] ⁺ .

EXAMPLE 6 methyltetrahvdrofuran-2-yl)-lH-purin-6 9H)-one (6)

[0200] Preparation of (6-1): To a solution of 1-3 (3.0 g, 8.02 mmol) and Ac ₂ 0 (4.91 g, 48.13 mmol) in acetic acid (30 mL) was added a solution of concentrated H ₂ S0 ₄ (2.41 g, 24.06 mmol) in acetic acid (10 mL) at 0 °C. The mixture was stirred at R.T. for 12 h. The mixture was poured into ice water and extracted with EA. The organic phase was dried and concentrated to give a residue, which was purified by silica gel column chromatography (10% EA in PE) to give 6-1 (2.3 g, 81%) as a colorless oil.

[0201] Preparation of (6-2): To a stirred mixture of 6-chloroguanine (560 mg, 3.31 mmol) and 6-1 (1.1 1 g, 2.76 mmol) in anhydrous MeCN (5 mL) under N ₂ was added 1,8- diazobicyclo[5.4.0] undec-7-ene (1.27 g, 8.28 mmol) at 0 °C. The mixture was stirred at R.T. for 0.5 h. The mixture was re-cooled to 0 °C and TMSOTf (2.45 g, 11.04 mmol) was added. The resulting mixture was heated to 60 °C for 4 h and then concentrated to dryness. The residue was partitioned between EA and saturated sodium hydrogen carbonate. The organic phase was separated and concentrated to give a residue, which was purified by silica gel column chromatography (2% MeOH in DCM) to give 6-2 (800 mg, 70%) as a white solid.

[0202] Preparation of (6-3): To a solution of 6-2 (839 mg, 1.64 mmol) in anhydrous dichloromethane (10 mL) were added MMTrCl (1.46 g, 4.75 mmol), Ag 03 (697 mg, 4.1 mmol) and collidine (794 mg, 6.56 mmol). The mixture was stirred at R.T. for 12 h. The reaction was quenched with saturated sodium hydrogen carbonate solution. The mixture was filtered, and the filtrate was extracted with EA. The organic layer was washed with water and brine, dried and concentrated to give a residue, which was purified on silica gel column chromatography (20% EA in PE) to give 6-3 (1.3 g, 72.5%) as a white solid.

[0203] Preparation of (6-4): To a solution of 3-hydroxyl acrylic nitrile (413 g, 5.82 mmol) in anhydrous THF was added sodium hydrogen (464 mg, 1 1.6 mmol). The mixture was warmed to R.T. for 0.5 h, and then the mixture was re-cooled to 0 °C. To the mixture was added a solution of 6-3 (0.912 g, 1.16 mmol) in anhydrous THF (5 mL). The mixture was warmed to R.T. for 12 h. The reaction was quenched with water and extracted with EA. The organic phase was separated and concentrated to give a residue, which was purified by silica gel column chromatography (5% MeOH in DCM) to give 6-4 (600 mg, 85%) as a white solid.

[0204] Preparation of (6): To a solution of 6-4 (785 mg, 1.19 mmol) and ammonium formate (1.50 g, 23.75 mmol) in acetone (50 mL) was added dry Pd/C (785 mg). The mixture was heated to reflux for 12 h. The mixture was filtered, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (10% MeOH in DCM) to give 6 (400 mg, 59%) as a white solid. ESI-MS: m/z 299.77 [M+H] ⁺ .

EXAMPLE 7

(2S)-neopentyl 2-(( (2R,3R,4S,5R)-5-(2-amino-6-oxo-lH-purin-9(6H)-yl)-3-nuoro-4- hvdroxy-4-methyltetrahvdrofuran-2-yl)methoxy)(2- chlorophenoxy)phosphoryl)amino)propanoate (7)

[0205] Preparation of (7): To a stirred solution of 6-4 (161 mg, 0.28 mmol) in anhydrous THF (1 mL) was added a solution of /-BuMgCl (1.41 mL, 1M in THF) dropwise at 0 °C. The mixture was stirred at R.T. for 0.5 h and then re-cooled to 0 °C. To the mixture was added a solution of 2-2 (517 mg, 1.41 mmol) dropwise. The mixture was stirred at R.T. for 2 h. The reaction was quenched with water and extracted with EA. The organic layer was dried and concentrated. The residue was purified on a silica gel column to give a protected intermediate (100 mg). The protected intermediate was treated with a 60% acetic acid aqueous solution and stirred at R.T. for 12 h. The solvent was removed under reduced pressure. The residue was purified by silica gel column chromatography and then RP HPLC separation (0.1% HCOOH in water and MeCN) to give 7 (12.13 mg, 10%) as a white solid. ESI-LCMS: m/z 631.1 [M+H] ⁺ .

EXAMPLE 8

(2S)-cvclohexyl 2-( ((2R,3R,4S,5R)-5-(2-amino-6-oxo-lH-purin-9(6H)-vn-3-nuoro-4- hvdroxy-4-methyltetrahvdrofuran-2-yl)methoxy)(3-chloro-4- fluorophenoxy)phosphoryl)amino)propanoate (8)

[0206] Preparation of (8): To a stirred solution of 6-4 (100 mg, 0.18 mmol) in anhydrous THF (1 mL) was added a solution of /-BuMgCl (0.9 mL, 0.9 mmol) dropwise at -78 °C. The mixture was stirred at R.T. for 0.5 h and then re-cooled to -78 °C. To the mixture was added a solution of 3-1 (357 mg, 0.9 mmol) dropwise. The mixture was stirred at R.T. for 12 h. The reaction was quenched with water and extracted with EA. The organic layer was dried and concentrated. The residue was purified on a silica gel column to give a protected intermediate (100 mg). The protected intermediate was treated with a 65% HCOOH aqueous solution and stirred at R.T. for 12 h. The solvent was removed under reduced pressure. The residue was purified by silica gel column chromatography and then RP HPLC (0.1% HCOOH in water and MeCN) to give 8 (16.83 mg, 14%) as a white solid. ESI-LCMS: m/z 661.1 [M+H] ⁺ .

EXAMPLE 9

i2SVcvclohexyl 2-rrrrr2R.3R.4S.5RV5-r2-amino-6-oxo-lH-purin-9r6HVylV3-nuoro -4- hvdroxy-4-methyltetrahvdrofuran-2-yl)methoxy) phenoxy)phosphoryl)amino)propanoate

[0207] To a stirred solution of 6 (21 mg, 0.07 mmol) in NMI (0.25 mL) was added a solution of 5-1 (0.35 mL, 1M in THF) dropwise at 0°C. The mixture was stirred at R.T. for 5 h, then more 5-1 (0.21 mL) was added. The mixture was stirred for 3 days. Additionally, 5-1 (0.21 mL) was added, and the mixture was stirred at 35 °C for 1 day. After cooling to R.T., the mixture was diluted with EA, washed with NH ₄ Cl-AcOH (2 times), NH ₄ C1 (3 times), NaHC0 ₃ . The organic layer was dried over sodium sulfate and concentrated. Chromatography on silica gel with 5-10% MeOH in DCM gave 9 (27 mg) as a slightly -yellow solid. Further chromatography on silica gel provided pure 9 (19 mg) as a white solid. ESI-LCMS: m/z 607.2 [M-H] ^~ .

EXAMPLE 10

Compound (10)

[0208] To an ice cold solution of 1 (53 mg; 016 mmol) in anhydrous THF (2 mL) was added isopropylmagnesium chloride (0.12 mL; 2 M in THF). The mixture stirred at 0 °C for 20 min. A solution of phosphorochloridate reagent P-l (0.15 g; 3 equiv.) in THF (0.3 mL) was added dropwise. The mixture stirred overnight at R.T. The reaction was quenched with saturated aq. NH ₄ C1 solution and stirred at R.T. for 10 min. The mixture was diluted with water and CH2CI2. The resulting two layers were separated. The organic layer was washed with water, half saturated aq. aHC0 ₃ and brine, and then dried with a ₂ S0 ₄ . The evaporated residue was purified on silica gel column with CH ₂ Ci2-MeOH solvent system (2-10% gradient) to yield a Rp/Sp-mixture of 10 (48 mg; 50%). ³¹ P-NMR (DMSO-d ₆ ): δ 3.98, 3.81. MS: m/z = 595 [M-l]-.

EXAMPLE 11

Compound (11)

[0209] To an ice cold solution of 1 (95 mg; 029 mmol) in anhydrous THF (3 mL) was added isopropylmagnesium chloride (0.29 mL; 2 M in THF). The mixture stirred at 0 °C for 20 min. A solution of thiophosphorochloridate reagent S-1 (0.28 g; 3 equiv.) in THF (0.3 mL) was added, and the mixture stirred 1 day at 40 °C. The reaction was quenched with saturated aq. NH ₄ C1 solution and stirred at R. T. for 10 min. The mixture was diluted with water and CH2CI2, and the two layers were separated. The organic layer was washed with water, half saturated aq. NaHCC , and brine, and dried with Na ₂ S0 ₄ . The evaporated residue was purified on silica gel column with CH ₂ Ci2-MeOH solvent system (4-10% gradient) to yield Rp/Sp- mixture of 11 (42 mg; 24%). ³¹ P-NMR (DMSO-d ₆ ): δ 68.32, 68.19. MS: m/z = 611 [M-l] ^" .

EXAMPLE 12

Compound (12)

[0210] To a solution of 1 (91 mg; 0.28 mmol) in acetonitrile (2 mL) were added 1- methylimidazole (0.21 mL; 8 equiv.) and thiophosphorochloridate reagent S-2 (0.3 g; 3 equiv). The mixture stirred 1 day at 40 °C. The reaction was quenched at R.T. with MeOH, and the mixture evaporated. The oily residue was dissolved in CH2CI2 and washed with IN citric acid, half saturated aq. NaHCC>3 and brine, and dried with Na ₂ S0 ₄ . The evaporated residue was purified on silica gel column with CH ₂ Ci2-MeOH solvent system (4-10% gradient) to yield Rp/Sp-mixture of 12 (120 mg; 66%). ³¹ P-NMR (DMSO-d ₆ ): δ 68.27, 68.24. MS: m/z = 651 [M-l]-.

EXAMPLE 13

Compound (13)

[0211] Compound 13 was prepared in the same way as described for 12 from 1 (75 mg; 0.23 mmol) with 1-methylimidazole (0.15 mL) and thiophosphorochloridate reagent S-3 (0.24 g) in acetonitrile (2 mL). 55 mg yield (37%). ³¹ P-NMR (DMSO-d ₆ ): δ 68.40, 68.16. MS: m/z = 639 [M-l] ^" .

EXAMPLE 14

Compounds (14) and (15)

[0212] Dry 6 (18 mg, 0.05 mmol) was dissolved in the mixture of PO(OMe) ₃ (0.750 mL ) and pyridine (0.5 mL). The mixture was evaporated in vacuum for 15 mins at bath temperature (42 °C), and then cooled down to R.T. N-Methylimidazole (0.009 mL, 0.11 mmol) was added followed by POCI ₃ (0.009 mL, 0.1 mmol). The mixture was kept at R.T. for 45 mins. Tributylamine (0.065 mL, 0.3 mmol) and N-tetrabutyl ammonium salt of pyrophosphate (100 mg) was added. Dry DMF (about 1 mL) was added to get a homogeneous solution. In 1 h, the reaction was quenched with 2M ammonium acetate buffer (1 mL, pH = 7.5), diluted to 10 mL with water and loaded on the column HiLoad 16/10 with Q Sepharose High Performance. Separation was done in a linear gradient of NaCl from 0 to IN in 50mM TRIS-buffer (pH = 7.5). The fractions eluted at 60% buffer B contained 14 and at 80% buffer B contained 15. The corresponding fractions were concentrated, and the residue purified by RP HPLC on Synergy 4 micron Hydro-RP column (Phenominex). A linear gradient of methanol from 0 to 30% in 50mM triethylammonium acetate buffer (pH 7.5) was used for elution. The corresponding fractions were combined, concentrated and lyophilized 3 times to remove excess of buffer. Compound 14: P ³¹ -NMR (D ₂ 0): -3.76 (s); ^X H -NMR (D ₂ 0): 8.00(s, 1H), 5.88(s, 1H), 5.10-4.95 (m, 2H), 4.05-3.98 (m, 2H), 1.00 (s, 3H); MS: 378.2 [M-l] ^" . Compound 15: P ³¹ -NMR (D ₂ 0): - 10.24(Ρα), -1 1.46(Ρβ), -23.18(Ργ); ^X H -NMR (D ₂ 0): (D ₂ 0): 8.44(s, 1H), 8.17 (s, 1H), 5.05(s, 1H), 4.18 (m, 2H), 4.02 (m, 3H); MS 538.0 [M-l] ^" .

EXAMPLE 15

HCV Replicon Assay

Cells

[0213] Huh-7 cells containing the self-replicating, subgenomic HCV replicon with a stable luciferase (LUC) reporter were cultured in Dulbecco's modified Eagle's medium (DMEM) containing 2mM L-glutamine and supplemented with 10% heat- inactivated fetal bovine serum (FBS), 1% penicillin-streptomyocin, 1% nonessential amino acids, and 0.5 mg/mL G418.

Determination of anti-HCV activity

[0214] Determination of 50% inhibitory concentration (EC5 ₀ ) of compounds in HCV replicon cells were performed by the following procedure. On the first day, 5,000 HCV replicon cells were plated per well in a 96-well plate. On the following day, test compounds were solubilized in 100% DMSO to lOOx the desired final testing concentration. Each compound was then serially diluted (1 :3) up to 9 different concentrations. Compounds in 100% DMSO are reduced to 10% DMSO by diluting 1 : 10 in cell culture media. The compounds were diluted to 10% DMSO with cell culture media, which were used to dose the HCV replicon cells in 96-well format. The final DMSO concentration was 1%. The HCV replicon cells were incubated at 37 °C for 72 h. At 72 h, cells were processed when the cells are still subconfluent. Compounds that reduce the LUC signal are determined by Bright-Glo Luciferase Assay (Promega, Madison, WI). % Inhibition was determined for each compound concentration in relation to the control cells (untreated HCV replicon) to calculate the EC5 ₀ . [0215] Compounds of Formula (I) are active in the replicon assay. The antiviral activity of exemplary compounds is shown in Table 2, where 'A' indicates an EC5 ₀ < 1 μΜ, 'B' indicates an EC50≥ 1 μΜ and < 10 μΜ, and 'C indicates an EC50 > 10 μΜ and < 100 μΜ.

Table 2

EXAMPLE 16

NS5B Inhibition Assay

[0216] The enzyme activity of NS5B570-Conl (Delta-21) was measured as an incorporation of tritiated NMP into acid-insoluble RNA products. The complementary IRES

(cIRES) RNA sequence was used as a template, corresponding to 377 nucleotides from the 3'- end of HCV (-) strand RNA of the Con-1 strain, with a base content of 21% Ade, 23% Ura,

28% Cyt, and 28% Gua. The cIRES RNA was transcribed in vitro using a T7 transcription kit

(Ambion, Inc.) and purified using the Qiagen RNeasy maxi kit. HCV polymerase reactions contained 50 nM NS5B570-Conl, 50 nM cIRES RNA, about 0.5 μϋϊ tritiated NTP, 1 μΜ of competing cold NTP, 20 mM NaCl, 40 mM Tris-HCl (pH 8.0), 4 mM dithiothreitol, and 4 mM

MgCl ₂ . Standard reactions were incubated for 2 h at 37°C, in the presence of increasing concentration of inhibitor. At the end of the reaction, RNA was precipitated with 10% TCA, and acid-insoluble RNA products were filtered on a size exclusion 96-well plate. After washing of the plate, scintillation liquid was added and radio labeled RNA products were detected according to standard procedures with a Trilux Topcount scintillation counter. The compound concentration at which the enzyme-catalyzed rate was reduced by 50% (IC ₅₀ ) was calculated by fitting the data to a non-linear regression (sigmoidal). The IC5 ₀ values were derived from the mean of several independent experiments and are shown in Table 3. Compounds of Formula (I) showed activity in this assay. A value of 'A' in the table below indicates an IC5 ₀ of < 1 μΜ, a value of 'B' indicates an IC5 ₀ ≥ 1 μΜ and < 10 μΜ, and a value of 'C indicates an IC5 ₀ value of

> 10 μM and < 100 μΜ.

Table 3 EXAMPLE 17

Assessment of inhibition of mitochondrial function

[0217] Drug-associated dysfunction of mitochondria is believed to play a role in the etiology of the various adverse symptoms that occur in patients treated with antiviral nucleoside/nucleotides. For this reason, evaluation of compounds for their potential to inhibit mitochondrial function is useful. To assess the potential for nucleotide/nucleoside analogs to interfere with normal mitochondrial functions and exhibit mitochondrial toxicity, the following were measured: (1) the ability of nucleotides to be incorporated by human mitochondrial RNA polymerase in vitro and (2) the cellular inhibition of the synthesis of the mitochondrial DNA

(mtDNA)-encoded protein, cytochrome c oxidase (COX-I), relative to the nuclear DNA

(nDNA)-encoded mitochondrial protein succinate dehydrogenase subunit A (SDH-A) in HepG2 cells. Control compounds and compounds of Formula (I) were studied in these assays.

Biochemical assay

[0218] Arnold et al. "Sensitivity of Mitochondrial Transcription and Resistance of RNA Polymerase II Dependent Nuclear Transcription to Antiviral Ribonucleosides" PLoS Pathog (2012) 8(11): el003030. doi: 10.1371/journal.ppat.1003030, which is hereby incorporated by reference in its entirety.

Assessment of incorporation of nucleotides by human mitochondrial RNA polymerase iHMRP)

DdRp assay with human mitochondrial RNA polymerase

[0219] The DdRp assay with human mitochondrial RNA polymerase was performed under single turnover conditions where enzyme concentration is in excess of the primer/template. The ³³ P-RNA/DNA primer/template was used at a concentration of 100 nM, together with 320 nM enzyme. The standard ΙΟ-μί reactions were carried out at 30°C for 1 minute with 100 μΜ of each nucleotide 5 '-triphosphate (NTP), 10 mM MgCl ₂ , 50 mM NaCl, 40 mM Tris, pH 7.5, and 1 mM DTT. The reaction was stopped by adding 20 μϊ _^ of formamide loading dye containing 50 mM EDTA. RNA products were resolved by electrophoresis on 22.5% TBE Urea polyacrylamide sequencing gels that were scanned using a TYPHOON Phosphorlmager.

[0220] The template strand shown in Figure 10 was designed to measure the incorporation of GTP analogs. Primer/Template: (SEQ ID NO: 1) UUUUGCCGCGCC and (SEQ ID NO: 2) GGGAATGCACGGCGCGGC. In the control water lanes, no incorporation was observed as indicated by the lack of product band. GTP and 3'-deoxy-GTP were found to be efficient substrates for incorporation as demonstrated by the significant product bands. The potential for misincorporation was assessed using the control nucleotide ATP. As shown by the lack of product band in Figure 10, control ATP was a poor substrate for incorporation. Nucleotide analog 2'-Me-GTP (the nucleotide metabolite of monophosphate prodrug ΓΝΧ- 0189/BMS-986094) was tested and found to be a good substrate for incorporation by HMRP as indicated by the product band. Nucleotide analog 2'-Me-2'-F-GTP (nucleotide metabolite of monophosphate prodrug GS-938) was tested and also found to be incorporated by HMRP. In contrast, compounds of Formula (I) were not efficient substrates for incorporation into the template strand by HMRP as indicated by the lack of product bands in Figure 10.

Assessment of inhibition of mitochondrial protein synthesis - Cell Based Assay

Assay Principle

[0221] MitoBiogenesis™ In Cell ELISA kits (Cat. #MS643) were obtained from Mitosciences, OR, USA. The MitoBiogenesis™ In Cell ELISA kit is a duplexing 96 well assay that ratios both an mtDNA and an nDNA encoded mitochondrial protein. Cells were seeded in 96 microplates and after exposure to compounds for several cell doublings, the levels of the two mitochondrial proteins were measured simultaneously in each well. The two proteins assayed were each subunits of different oxidative phosphorylation enzyme complexes, one protein being subunit I of Complex IV (cytochrome c oxidase; COX I) that is mtDNA encoded and the other being the 70 kDa subunit of Complex II (succinate dehydrogenase subunit A; SDH A) that is nDNA encoded. Complex IV includes several proteins that are encoded by the mtDNA while the proteins of Complex II are entirely encoded by nDNA. To control for the density of cells present at the end of the culture period, the number of cells were assessed by staining with Janus Green and the levels of COX I/SDH A normalized to the final cell density.

96 Well Plate Assay Format for HepG2 Cells

[0222] On the first day, 1000 HepG2 cells per well were plated in a 96 well plate. On the following day, compounds to be tested were solubilized in 100% DMSO to 100 x the desired final testing concentration. Each compound was serially diluted (1 :3) up to 9 distinct concentrations. Compounds in 100% DMSO were reduced to 10% (v/v) DMSO by diluting 1 : 10 in cell culture media. A 10 aliquot of the compounds diluted to 10% (v/v) DMSO with cell culture media was used to dose the cells in duplicate. The final DMSO concentration was 1% (v/v). Untreated cells and wells containing no cells were included on the plate to serve as controls. Cells were then incubated with compounds and observed for 8 days at 37°C and 5% CO ₂ . Plates were processed as described below in the assay procedure.

Batch Assay Format for HepG2 Cells

[0223] An alternate cell culture procedure was employed to test the potential to mediate mitochondrial toxicity at higher concentrations than achievable in the 96 well plate format. HepG2 cells were grown either in media/DMSO alone or in a series of compound concentrations in 15 cm ² dishes or 6 well plates at an initial cell seeding density of 5 x 10 ⁶ and 5 x 10 ⁴ cells/mL, respectively. Cells were then incubated and observed for 8 days at 37°C and 5% CO2. After 8 days, the cells were harvested by trypsinization, counted, and seeded in 96 well plates at a density of 25,000 cells/well in 16 replicate wells. Cells were allowed to adhere overnight and then the plates were processed as described below in the assay procedure.

Assay Procedure

[0224] The assay was performed according to the manufacturer's instructions. Briefly, after the end of the culture period the cell culture media was gently aspirated from the wells of the plate and replaced with 100 μΐ, of 4% (v/v) paraformaldehyde solution in phosphate buffered saline (PBS, Electron Microscopy Sciences Cat. #15713). After a 20 mins incubation at R.T., the solution was removed and the wells washed 3 x with 300 μϊ _^ of PBS. After the final wash, the PBS was removed and the wells overlayed with 100 PBS. The plates were then sealed and stored at 4°C until used. To perform the assay, the PBS overlay was removed by blotting on a paper towel and 100 of 0.5% (v/v) acetic acid added to each well to block endogenous alkaline phosphatase activity. After a 5 mins incubation at R.T., the acetic acid solution was removed and the cells washed once with 200 μΐ _^ PBS. Then, 100 μΐ _^ of permeabilization buffer (0.1% (v/v) Triton X 100) was added to each well. After 30 mins incubation at R.T., the permeabilization buffer was removed and each well was blocked with 200 μϊ _^ οΐ2 χ blocking solution for 2 h at R.T. The 2 x blocking solution was then removed and 100 μϊ _^ of primary antibody solution containing anti COX I and anti SDH A antibodies in 1 blocking solution was added to each well. Plates were then sealed and incubated overnight at 4°C. The primary antibody/blocking solution was removed and the plate washed 3 x with 250 μΐ _^ 0.05% (v/v) Tween 20 in PBS. Then, 100 μΐ _^ of secondary antibody solution containing alkaline phosphatase (AP) labeled anti SDH A antibody and horseradish peroxidase (HRP) labeled anti COX I antibody was added and incubated for 1 h at R.T. The plate was then washed 4 x with 250 μΐ, 0.05% (v/v) Tween 20 in PBS. After blotting the plate dry 100 μΐ, of AP detection reagent was added to each well, and the plate incubated in the dark for 30 mins at R.T. The optical density of each well was then measured at 405 nm. The AP detection reagent was then removed and replaced with 100 μϊ _^ of HRP detection reagent, and the plate incubated in the dark for a further 30 mins at R.T. The optical density of each well was then measured at 600 nm. The HRP detection reagent was then removed and each well was then stained with 50 μΕ of 1 x Janus Green Stain for 5 mins at R.T. After removal of the dye, the plates were washed 5 x in ultrapure water to remove any remaining dye. The Janus Green stain was then solubilized by the addition of 100 μί _^ of 0.5 M HCl and incubated for 10 mins. The optical density of each well was then measured at 595 nm.

Data Analysis

[0225] The average of all replicate background measurements from each experimental condition was calculated and subtracted from the experimental values of the same condition. The SDH A and COX I signals were then plotted as a ratio (COX I/SDH A) and normalized to the Janus Green staining intensity to correct for differences in cell density.

Results

[0226] Control compound d4T was tested and found not to inhibit mitochondrial protein synthesis at concentrations as shown in Figures 1 1A-B. Control compound ddC was tested and found to strongly inhibit mitochondrial protein synthesis. See Figures 11A-B. As demonstrated in Figure 11B, nucleoside monophosphate prodrug INX-08189/BMS-986094

(which delivers 2'-Me-GTP) was tested in the assay and found to strongly inhibit mitochondrial protein synthesis. In contrast, compounds of Formula (I) were tested and found to not inhibit mitochondrial protein synthesis as shown in Figure 11 A.

EXAMPLE 18

Combination of Compounds

Combination Testing

[0227] Two or more test compounds are tested in combination with each other using an HCV genotype lb HCV replicon harbored in Huh7 cells with a stable luciferase (LUC) reporter. Cells are cultured under standard conditions in Dulbecco's modified Eagle's medium (DMEM; Mediatech Inc, Herndon, VA) containing 10% heat- inactivated fetal bovine serum (FBS; Mediatech Inc, Herndon, VA) 2mM L-glutamine, and nonessential amino acids (JRH Biosciences). HCV replicon cells are plated in a 96-well plate at a density of 10 ⁴ cells per well in DMEM with 10% FBS. On the following day, the culture medium is replaced with DMEM containing either no compound as a control, the test compounds serially diluted in the presence of 2% FBS and 0.5% DMSO, or a combination of a compound of Formula (I) with one or more test compounds serially diluted in the presence of 2% FBS and 0.5% DMSO. The cells are incubated with no compound as a control, with the test compounds, or the combination of compounds for 72 h. The direct effects of the combination of the test compounds are examined using a luciferase (LUC) based reporter as determined by the Bright-Glo Luciferase Assay (Promega, Madison, WI). Dose-response curves are determined for individual compounds and fixed ratio combinations of two or more test compounds.

[0228] The method utilized for evaluating combination effects used a program called MacSynergy II. MacSynergy II software was kindly provided by Dr. M. Prichard (University of Michigan). The Prichard Model allows for a three-dimensional examination of drug interactions and a calculation of the synergy volume (units: μΜ ² %) generated from running the replicon assay using a checkerboard combination of two or more inhibitors. The volumes of synergy (positive volumes) or antagonism (negative volumes) represent the relative quantity of synergism or antagonism per change in the concentrations of the two drugs. Synergy and antagonism volumes are defined based on the Bliss independence model. In this model, synergy volumes of less than -25 indicate antagonistic interactions, volumes in the -25 - 25 range indicate additive behavior, volumes in the 25 - 100 range indicate synergistic behavior and volumes >100 indicate strong synergistic behavior. Determination of in vitro additive, synergistic and strongly synergistic behavior for combinations of compounds can be of utility in predicting therapeutic benefits for administering the combinations of compounds in vivo to infected patients.

[0229] Although the foregoing has been described in some detail by way of illustrations and examples for purposes of clarity and understanding, it will be understood by those of skill in the art that numerous and various modifications can be made without departing from the spirit of the present disclosure. Therefore, it should be clearly understood that the forms disclosed herein are illustrative only and are not intended to limit the scope of the present disclosure, but rather to also cover all modification and alternatives coming within the true scope and spirit of the invention.