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  • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
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Definitions

• This invention relates to imidazopyridine compounds that have ether or thioether substitution at the 1 -position, and that may contain additional functionality.
• the invention also provides pharmaceutical compositions containing these compounds and methods of inducing cytokine biosynthesis by administration of the compounds.
• Certain lH-imidazo[4,5-c]quinolin-4-amines and 1- and 2-substituted derivatives thereof were later found to be useful as antiviral agents, bronchodilators and immunomodulators. These are described in, inter alia, U.S. Patent Nos. 4,689,338; 4,698,348; 4,929,624; 5,037,986; 5,268,376; 5,346,905; and 5,389,640, all of which are incorporated herein by reference. Substituted lH-imidazopyridine-4-amine compounds useful as immune response modifiers are described in United States Patent Nos.
• the invention provides imidazopyridine compounds that have ether substitution at the 1 -position. These compounds have the general formula (la):
• the invention provides pharmaceutical compositions containing the compounds and methods of using the compounds to achieve a therapeutic effect. Such effects include the induction of cytokine biosynthesis, the induction of interferon biosynthesis, treatment of viral conditions and treatment of neoplastic conditions. In other aspects, the invention additionally provides methods of making the compounds and intermediate compounds useful in their synthesis.
• the compounds of the invention have an ether linkage at the 1 -position of the compounds.
• the compounds may include additional substitution that occurs after the initial ether linkage, such as aryl, heteroaryl, heterocyclyl, amido, sulfonamido, urea, and the like.
• An additional set of compounds provided by the invention contain a thioether linkage at the 1 -position; these thioether compounds may also have additional substitution after the initial thioether linkage, including alkyl, aryl, heteroaryl, and heterocyclyl.
• compounds of the invention are repesented by Formula la:
• X is -CH(R 5 )-, -CH(R 5 )-alkylene-, -CH(R 5 )-alkenylene-, or CH(R 5 )-alkylene-Y-alkylene-;
• Y is -O- or-S(O)o- 2 -;
• -W-Rj is selected from -O-R 1-1-5 and -S(O)o- 2 -R 1-6 ; R - 5 is selected from
• Z is-N(R 5 )-, -O-, or -S ⁇ ;
• Q is a bond, -CO- or -SO 2 -;
• A represents the atoms necessary to provide a 5- or 6-membered heterocyclic or heteroaromatic ring that contains up to three heteroatoms;
• R 1-6 is selected from: -alkyl;
• each R 5 is independently hydrogen, C 1-10 alkyl, or C -10 alkenyl
• R 6 is alkylene, alkenylene, or alkynylene, which may be interrupted by one or more -O- groups
• R 8 is a bond, alkylene, alkenylene, or alkynylene, which may be interrupted by one or more -O- groups;
• R 9 is hydrogen, Ci.io alkyl, or arylalkyl; or R 9 can join together with any carbon atom of R 6 to form a ring of the formula
• R 10 is hydrogen or C MO alkyl; or R 9 and R 10 can join together to form a ring selected from
• Ri i is C O alkyl; or R 9 and Ri i can join together to form a ring having the structure
• R 12 is C 2 . 7 alkylene which is straight chain or branched, wherein the branching does not prevent formation of the ring; and R ⁇ 5 R Y and Rz are independently selected from hydrogen and non-interfering substitutents; or a pharmaceutically acceptable salt thereof, wherein the compound or salt of Formula la induces the biosynthesis of one or more cytokines.
• compounds of the invention are represented by Formula lb:
• X is -CH(R 5 )-, -CH(R 5 )-alkylene-, -CH(R 5 )-alkenylene- > or CH(R 5 )-alkylene-Y-alkylene-;
• -W-Ri is selected from -O-RM- 5 and -S(O) 0 - 2 -R 1-6 ;
• R 1-1-5 is selected from
• R ⁇ - 6 is selected from:
• R 2 is selected from the group consisting of: -hydrogen;
• Y is-O- or-S(O)o- 2 -;
• Z is-N(R 5 )- -O-, or -S-;
• Q is a bond, -C(O)-, or -SO 2 -;
• A represents the atoms necessary to provide a 5- or 6-membered heterocyclic or heteroaromatic ring that contains up to three heteroatoms;
• R 3 and I are independently selected from the group consisting of hydrogen, C 1-10 alkyl, C 2-1 o alkenyl, C 2-1 o alkynyl, CM O alkoxy, CM O alkylthio, amino, alkylamino, dialkylamino, halogen, and nitro; each R 5 is independently hydrogen, CM O alkyl, or C 2 - ⁇ o alkenyl; Rg is alkylene, alkenylene, or alkynylene, which may be interrupted by one or more -O- groups;
• R 8 is a bond, alkylene, alkenylene, or alkynylene, which may be interrupted by one or more -O- groups;
• R 9 is hydrogen, CM O alkyl, or arylalkyl; or R can join together with any carbon atom of Re to form a ring of the formula (CH 2 ) 3-8
• Rio is hydrogen or CM O alkyl; or R 9 and R 10 can join together to form a ring selected from
• R ⁇ is C O alkyl; or R 9 and Rj j can join together to form a ring having the structure
• R 12 is C 2-7 alkylene which is straight chain or branched, wherein the branching does not prevent formation of the ring; or a pharmaceutically acceptable salt thereof.
• One embodiment includes a class of compounds represented by Formula (I-l):
• X is -CH(R 5 )-, -CH(R 5 )-alkylene-, -CH(R 5 )-alkenylene-, or CH(R 5 )-alkylene-Y-alkylene-;
• R is selected from the group consisting of: -R 6 -C(R 7 )-Z-R 8 -alkyl; -R 6 -C(R 7 )-Z-R 8 — alkenyl; -R 6 -C(R 7 )-Z-R 8 -aryl; -R 6 -C(R 7 )-Z-R 8 — heteroaryl; -R 6 -C(R 7 )-Z-R 8 — heterocyclyl; -R 6 -C(R 7 )-Z-H;
• R 2 is selected from the group consisting of: -hydrogen; -alkyl;
• R 3 and R- t are independently selected from the group consisting of hydrogen, CM O alkyl, C 2 - 10 alkenyl, C 2 . ⁇ o alkynyl, C O alkoxy, CMO alkylthio, amino, alkylamino, dialkylamino, halogen, and nitro; each R 5 is independently hydrogen, CM O alkyl, or C 2 - 1 o alkenyl; R ⁇ is alkylene, alkenylene, or alkynylene, which may be interrupted by one or more -O- groups;
• R 8 is a bond, alkylene, alkenylene, or alkynylene, which may be interrupted by one or more -O- groups;
• R 9 is hydrogen, C O alkyl, or arylalkyl; or R 9 can join together with any carbon atom of R 6 to form a ring of the formula
• Rio is hydrogen or CM O alkyl; or R 9 and Rto can join together to form a ring selected from
• Another embodiment includes a class of compounds represented by Formula (1-2):
• X is -CH(Rs)-, -CH(R 5 )-alkylene-, -CH(R 5 )-alkenylene-, or CH(R 5 )-alkylene-Y-alkylene-;
• R 1-2 is selected from the group consisting of:
• R 2 is selected from the group consisting of:
• Y is -O- or -S(O) 0 -2-;
• R 3 and j are independently selected from the group consisting of hydrogen, CM O alkyl, C2- 10 alkenyl, C 2 - ⁇ o alkynyl, CM O alkoxy, CM O alkylthio, amino, alkylamino, dialkylamino, halogen, and nitro; each R 5 is independently hydrogen, CM O alkyl, or C 2-1 o alkenyl;
• R ⁇ is alkylene, alkenylene, or alkynylene, which may be interrupted by one or more -O- groups;
• R 8 is a bond, alkylene, alkenylene, or alkynylene, which may be interrupted by one or more -O- groups;
• R 9 is hydrogen, C O alkyl, or arylalkyl; or R 9 can join together with any carbon atom of R 6 to form a ring of the formula
• Rio is hydrogen or CM O alkyl; or R 9 and R 10 can join together to form a ring having the structure — N— S0 2
• R 12 is C 2-7 alkylene which is straight chain or branched, wherein the branching does not prevent formation of the ring; or a pharmaceutically acceptable salt thereof.
• Another embodiment includes a class of compounds represented by Formula (1-3):
• X is -CH(R 5 )-, -CH(R 5 )-alkylene-, -CH(R 5 )-alkenylene-, or CH(R 5 )-alkylene-Y-alkylene-;
• R 1-3 is selected from the group consisting of:
• R 2 is selected from the group consisting of: -hydrogen; -alkyl;
• Y is-O- or-S(O)o- 2 -;
• Q is a bond, -C(O)-, or -SO 2 -;
• A represents the atoms necessary to provide a 5- or 6- membered heterocyclic or heteroaromatic ring that contains up to three heteroatoms;
• R 3 and IU are independently selected from the group consisting of hydrogen, CM O alkyl, C 2 .]o alkenyl, C 2 _ 10 alkynyl, CM O alkoxy, CM O alkylthio, amino, alkylamino, dialkylamino, halogen, and nitro; each R 5 is independently hydrogen, CM O alkyl, or C2-10 alkenyl;
• R 9 is hydrogen, CM O alkyl, or arylalkyl; or R 9 can join together with any carbon atom of R 6 to form a ring of the formula
• R 11 is CM O alkyl; or R 9 and R ⁇ can join together to form a ring having the structure
• Another embodiment includes a class of compounds represented by Formula (1-4):
• X is -CH(R 5 )-, -CH(R 5 )-alkylene-, -CH(R 5 )-alkenylene-, or CH(R 5 )-alkylene-Y-alkylene-;
• R 1 - 4 is selected from the group consisting of: -alkenyl; -aryl; and R 2 is selected from the group consisting of: -hydrogen; -alkyl; -alkenyl;
• R 3 and j are independently selected from the group consisting of hydrogen, C O alkyl, C2-10 alkenyl, C2-10 alkynyl, C O alkoxy, C O alkylthio, amino, alkylamino, dialkylamino, halogen, and nitro; each R5 is independently hydrogen, C MO alkyl, or C2- 10 alkenyl; and R 6 is alkylene, alkenylene, or alkynylene, which may be interrupted by one or more -O- groups; or a pharmaceutically acceptable salt thereof.
• Another embodiment includes a class of compounds represented by Formula (1-5):
• X is -CH(R 5 )-, -CH(R 5 )-alkylene-, -CH(R 5 )-alkenylene-, or CH(R 5 )-alkylene-Y-alkylene-;
• R_- 5 is selected from the group consisting of:
• R 2 is selected from the group consisting of:
• Y is -O- or -S(O) 0- 2-;
• R 3 -aid R-j are independently selected from the group consisting of hydrogen, CM O alkyl, C 2 -- 0 alkenyl, C 2 ..- 0 alkynyl, CM O alkoxy, C MO alkylthio, amino, alkylamino, dia-kylamino, halogen, and nitro; each R 5 is independently hydrogen, C MO alkyl, or C 2 -1 0 alkenyl; and R ⁇ is alkylene, alkenylene, or alkynylene, which may be interrupted by one or more -O- groups; or a pharmaceutically acceptable salt thereof.
• X is -CH(R 5 )-, -CH(R 5 )-alkylene-, -CH(R 5 )-alkenylene-, or CH(R 5 )-alkylene-Y-alkylene-;
• R 1-6 is selected from the group consisting of: -alkyl; -aryl; -heteroaryl; -heterocyclyl; -alkenyl; -R 6 -aryl; -Rg- heteroaryl;
• R 2 is selected from the group consisting of: -hydrogen; -alkyl; -alkenyl;
• R and R are independently selected from the group consisting of hydrogen, CM O alkyl, C 2-1 o alkenyl, C 2 - 10 alkynyl, C O alkoxy, C O alkylthio, amino, alkylamino, dialkylamino, halogen, and nitro; each R 5 is independently hydrogen, C O alkyl, or C 2 . 10 alkenyl; and
• R ⁇ is alkylene, alkenylene, or alkynylene, which may be interrupted by one or more -O— atoms; or a pharmaceutically acceptable salt thereof.
• Another aspect of the invention includes intermediate compounds of Formulas II, IV, V, LVIII, LIX-l, LIX-2, LIX-3, LIX-4, LIX-5, LXXVIII, LXXIX, LXXX-4, and LXXX-5.
• a class of intermediate compounds is represented by Formula II:
• X is -CH(R 5 )-, -CH(R 5 )-alkylene-, -CH(R 5 )-alkenylene-, or CH(R 5 )-alkylene-Y-alkylene-;
• R 2 is selected from the group consisting of: -hydrogen; -alkyl; -alkenyl; -aryl; -heteroaryl; -heterocyclyl; -alkylene- Y-alkyl; -alkylene- Y- alkenyl; -alkylene- Y-aryl; and
• Y is -O- or-S(O)o -2 -;
• R 3 and Rj are independently selected from the group consisting of hydrogen, CM O alkyl, C 2-1 o alkenyl, C 2 - 10 alkynyl, C O alkoxy, CM O alkylthio, amino, alkylamino, dialkylamino, halogen, and nitro;
• each R 5 is independently hydrogen, CM O alkyl, or C2- 10 alkenyl;
• R ⁇ 5 is alkylene, alkenylene, or alkynylene, which may be interrupted by one or more -O— atoms; and
• R 9 is hydrogen, CM O alkyl, or arylalkyl; or R can join together with any carbon atom of R ⁇ to form a ring of the formula
• X is -CH(R 5 )-, -CH(R 5 )-alkylene-, -CH(R 5 )-alkenylene-, or CH(R 5 )-alkylene-Y-alkylene-;
• R ⁇ - 6 is selected from the group consisting of:
• R 2 is selected from the group consisting of: -hydrogen;
• Y is -O- or -S(O)o- 2 -;
• R and R* are independently selected from the group consisting of hydrogen, CM O alkyl, C2-W alkenyl, C2- 10 alkynyl, CM O alkoxy, C MO alkylthio, amino, alkylamino, dialkylamino, halogen, and nitro; each R 5 is independently hydrogen, CM O alkyl, or C 2 -- 0 alkenyl; and R ⁇ is alkylene, alkenylene, or alkynylene, which may be interrupted by one or more ⁇ O— atoms; or a pharmaceutically acceptable salt thereof.
• X is -CH(R 5 )-, -CH(R 5 )-alkylene-, -CH(R 5 )-alkenylene-, or CH(R 5 )-alkylene-Y-alkylene-;
• R!- 6 is selected from the group consisting of:
• R 2 is selected from the group consisting of: -hydrogen;
• Y is -O- or-S(O)o -2 -;
• R 3 and R-j are independently selected from the group consisting of hydrogen, CM O alkyl, C2 0 alkenyl, C2- 10 alkynyl, CM O alkoxy, C MO alkylthio, amino, alkylamino, dialkylamino, halogen, and nitro; each R 5 is independently hydrogen, C MO alkyl, or C 2 - ! o alkenyl; and
• R ⁇ is alkylene, alkenylene, or alkynylene, which may be interrupted by one or more -O— atoms; or a pharmaceutically acceptable salt thereof.
• a class of intermediate compounds is represented by Formula LVIII:
• X is -CH(R 5 )-, -CH(R 5 )-alkylene-, -CH(R 5 )-alkenylene-, or CH(R 5 )-alkylene-Y-alkylene-;
• R 2 is selected from the group consisting of: -hydrogen; -alkyl;
• Y is -O- or-S(O) 0-2 -;
• R 3 and Rj are independently selected from the group consisting of hydrogen, CM O alkyl, C 2 - ⁇ o alkenyl, C 2 - ⁇ o alkynyl, C O alkoxy, CM O alkylthio, amino, alkylamino, dialkylamino, halogen, and nitro; each R 5 is independently hydrogen, CM O alkyl, or C 2 - ⁇ o alkenyl; R ⁇ is alkylene, alkenylene, or alkynylene, which may be interrupted by one or more -O— atoms; and
• R 9 is hydrogen, CM O alkyl, or arylalkyl; or R 9 can join together with any carbon atom of R ⁇ to form a ring of the formula
• a class of intermediate compounds is represented by Formulas LIX-l, LIX-2, and LLX-3:
• Ri-i, 2l 3 is Ri-i in LIX-l, R 1-2 in LIX-2, and R 1-3 in LIX-3;
• X is -CH(R 5 )-, -CH(R 5 )-alkylene-, -CH(R 5 )-alkenylene-, or CH(R 5 )-alkylene-Y-alkylene-;
• R M is selected from the group consisting of:
• Rj- 2 is selected from the group consisting of:
• R ⁇ _ 3 is selected from the group consisting of:
• R 2 is selected from the group consisting of:
• Y is-O- or-S(O) 0-2 -
• Z is-N(R 5 )-, -O-, or -S-
• Q is a bond, -CO- or -SO2-
• A represents the atoms necessary to provide a 5- or 6-membered heterocyclic or heteroaromatic ring that contains up to three heteroatoms;
• R 3 and - are independently selected from the group consisting of hydrogen, CM O alkyl, C2 -1 o alkenyl, C2-- 0 alkynyl, C MO alkoxy, C O alkylthio, amino, alkylamino, dialkylamino, halogen, and nitro; each R 5 is independently hydrogen, CM O alkyl, or C 2 - 10 alkenyl;
• R ⁇ is alkylene, alkenylene, or alkynylene, which may be interrupted by one or more -O- groups;
• R 8 is a bond, alkylene, alkenylene, or alkynyleiie, which may be interrupted by one or more -O- groups;
• R 9 is hydrogen, C MO alkyl, or arylalkyl; or R 9 can join together with any carbon atom of R ⁇ to form a ring of the formula
• R ⁇ is hydrogen or CMO alkyl; or R 9 and R 10 can join together to form a ring selected from
• R ⁇ is CMO alkyl; or R and R can join together to form a ring having the structure
• R 12 is C 2-7 alkylene which is straight chain or branched, wherein the branching does not prevent formation of the ring; or a pharmaceutically acceptable salt thereof.
• a class of intermediate compounds is represented by Formulas LIX-4, and LIX-5:
• Ri- ⁇ 5 is R ⁇ in LIX-4, and Ri-s in LIX-5;
• X is -CH(R 5 )- 5 -CH(R 5 )-alkylene-, -CH(R 5 )-alkenylene-, or
• R is selected from the group consisting of: -alkenyl; -aryl; and -R 6 -aryl;
• R ⁇ - 5 is selected from the group consisting of: -heteroaryl; -heterocyclyl; -R ⁇ - heteroaryl; and -R 6 -heterocyclyl;
• R 2 is selected from the group consisting of: -hydrogen; -alkyl; -alkenyl; -aryl;
• R 3 and 1- are independently selected from the group consisting of hydrogen, CM O alkyl, C2-10 alkenyl, C2-10 alkynyl, CM O alkoxy, C MO alkylthio, amino, alkylamino, dialkylamino, halogen, and nitro; each R 5 is independently hydrogen, CM O alkyl, or C 2 - 1 0 alkenyl; and R ⁇ is alkylene, alkenylene, or alkynylene, which may be interrupted by one or more -O- groups; or a pharmaceutically acceptable salt thereof.
• Y is -O- or-S(O)o- 2 -;
• BOC is tert-butoxycarbonyl; each R 5 is independently hydrogen, C O alkyl, or C 2 - 10 alkenyl;
• R 3 and I-U are independently selected from the group consisting of hydrogen, C O alkyl, C 2 - 10 alkenyl, C 2 - 10 alkynyl, CM O alkoxy, CM O alkylthio, amino, alkylamino, dialkylamino, halogen, and nitro;
• R 6 is alkylene, alkenylene, or alkynylene, which may be interrupted by one or more -O— atoms;
• R is hydrogen, C MO alkyl, or arylalkyl; or R 9 can join together with any carbon atom of R 6 to form a ring of the formula
• T is selected from nitro and amino; or a pharmaceutically acceptable salt thereof.
• X is -CH(R 5 )-, -CH(R 5 )-alkylene-, -CH(R 5 )-alkenylene-, or CH(R 5 )-alkylene-Y-alkylene-;
• Y is -O- or -S(O) 0 -2-;
• R 3 and I-U are independently selected from the group consisting of hydrogen, CM O alkyl, C2- 1 0 alkenyl, C - 1 o alkynyl, CM O alkoxy, CM O alkylthio, amino, alkylamino, dialkylamino, halogen, and nitro; each R 5 is independently hydrogen, CM O alkyl, or C2-10 alkenyl; and T is selected from nitro and amino; or a pharmaceutically acceptable salt thereof.
• a class of intermediate compounds is represented by Formulas LXXX-4 and LXXX-5 :
• R ⁇ - 4 , 5 is R 1-4 in LXXX-4, and R 1-5 in LXXX-5;
• X is -CH(R 5 )-, -CH(R 5 )-alkylene-, -CH(R 5 )-alkenylene-, or CH(R 5 )-alkylene-Y-alkylene-;
• R ⁇ .s is selected from the group consisting of:
• R 1-4 is selected from the group consisting of:
• -alkenyl; -aryl; and R 3 and I-U are independently selected from the group consisting of hydrogen, CM O alkyl, C2-10 alkenyl, C2-10 alkynyl, CM O alkoxy, C O alkylthio, amino, alkylamino, dialkylamino, halogen, and nitro; each R5 is independently hydrogen, CM O alkyl, or C2- 10 alkenyl; R ⁇ is alkylene, alkenylene, or alkynylene, which may be interrupted by one or more -O- groups; and
• T is selected from nitro and amino; or a pharmaceutically acceptable salt thereof.
• Some embodiments of the invention including compounds Formula 1-6 and intermediate compounds can be prepared according to Reaction Scheme I where R ⁇ - ⁇ , R 2 , R 3 , j, and X are as defined above and Ph is phenyl.
• a 2,4-dihydroxy-3-nitropyridine of Formula X is chlorinated using conventional chlorinating agents to provide a 2,4-dichloro-3- nitropyridine of Formula XI.
• a compound of Formula X is combined with phosphorous oxychloride and heated.
• Many 2,4-dihydroxy-3-nitropyridines are known and others can be readily prepared using known synthetic methods, see for example, Lindstrom et al., U.S. Patent No. 5,446,153 and the references cited therein.
• step (2) of Reaction Scheme I a 2,4-dichloro-3-nitropyridine of Formula XI is reacted with an amine of formula HO-X-NH 2 to provide a 2-chloro-3-nitropyridine of Formula XII.
• the reaction can be carried out by adding the amine to a solution of a compound of Formula XI in a suitable solvent such as N,N-dimethylformamide in the presence of triethylamine.
• a suitable solvent such as N,N-dimethylformamide
• step (3) of Reaction Scheme I a 2-chloro-3-nitropyridine of Formula XII is reacted with sodium phenoxide to provide a 3-nitro-2-phenoxypyridine of Formula XIII.
• Phenol is reacted with sodium hydride in a suitable solvent such as tetrahydrofuran to form the phenoxide.
• the phenoxide is then reacted at an elevated temperature with a compound of Formula XII.
• a 3-nitro-2-phenoxypyridine of Formula XIII is chlorinated using conventional chlorinating agents to provide a 3-nitro-2-phenoxypyridine of Formula XIV.
• the reaction is carried out by combining a compound of Formula XIII with thionyl chloride in a suitable solvent such as dichloromethane and heating.
• a 3-nitro-2- ⁇ henoxypyridine of Formula XIV is reduced to provide a 2-phenoxypyridine-3,4-diamine of Formula XV.
• the reduction is carried out using a conventional heterogeneous catalyst such as platinum on carbon.
• the reaction can be conveniently carried out on a Parr apparatus in a suitable solvent such as toluene or acetonitrile.
• Ni 2 B can be generated in situ from sodium borohydride and NiCl 2 in the presence of methanol.
• a compound of Formula XTV can be added to the resulting reducing agent solution to effect reduction of the nitro group.
• the Ni 2 B reducing agent can be used without reducing these moieties.
• the product can be isolated from the reaction mixture using conventional methods.
• a 2-phenoxypyridine-3,4-diamine of Formula XV is reacted with a carboxylic acid or an equivalent thereof to provide a 4-phenoxy-lH- imidazo[4,5-c]pyridine of Formula XVI.
• Suitable equivalents to a carboxylic acid include orthoesters, and 1,1-dialkoxyalkyl alkanoates.
• the carboxylic acid or equivalent is selected such that it will provide the desired R 2 substituent in a compound of Formula XVI. For example, triethyl orthoformate will provide a compound where R 2 is hydrogen and trimethyl orthovalerate will provide a compound where R 2 is butyl.
• the reaction can be run in the absence of solvent or in an inert solvent such as toluene.
• the reaction is run with sufficient heating to drive off any alcohol or water formed as a byproduct of the reaction.
• a catalyst such as pyridine hydrochloride can be included.
• step (6) can be carried out by (i) reacting the diamine of Formula XV with an acyl halide of Formula R 2 C(O)Cl or R 2 C(O)Br and then (ii) cyclizing.
• the acyl halide is added to a solution of the diamine in a suitable solvent such as pyridine.
• the reaction can be carried out at ambient temperature.
• the product of part (i) is heated in pyridine in the presence of pyridine hydrochloride.
• a 4-phenoxy-lH-imidazo[4,5-c]pyridine of Formula XVI is reacted with a compound of Formula R ⁇ _ 6 SNa to provide a 2-phenoxy-lH- imidazo[4,5-c]pyridine of Formula III.
• a thiol of the Formula R ⁇ S ⁇ is reacted with sodium hydride in a suitable solvent such as N,N-dimethylformamide to generate the anion, which is then reacted with a compound of Formula XVI.
• a 4-phenoxy-lH-imidazo[4,5-c]pyridine of Formula III is animated to provide a lH-imidazo[4,5-c]pyridin-4-amine of Formula XVII which is a subgenus of Formula 1-6.
• the reaction can be carried out by combining a compound of Formula III with ammonium acetate and heating (140 - 160°C).
• the reaction can be carried out in a pressure vessel.
• the product or a pharmaceutically acceptable salt thereof can be isolated using conventional methods.
• a lH-imidazo[4,5-c]pyridin-4-amine of Formula XVII is oxidized to provide a lH-imidazo[4,5-c]pyridin-4-amine of Formula XVIII which is a subgenus of Formula 1-6.
• a solution of a compound of Formula XVII in a suitable solvent such as chloroform or dichloromethane is treated with 3- chloroperoxybenzoic acid.
• the degree of oxidation is controlled by adjusting the amount of 3-chloroperoxybenxzoic acid used in the reaction; i.e., using approximately one equivalent will provide the sulfoxide whereas using two equivalents will provide the sulfone.
• the product or a pharmaceutically acceptable salt thereof can be isolated using conventional methods.
• steps (8) and (9) of Reaction Scheme I can be reversed as shown in steps (10) and (11).
• step (10) of Reaction Scheme I a 4- ⁇ henoxy-lH-imidazo[4,5- cjpyridine of Formula III is oxidized as in step (9) to provide a 4-phenoxy-lH- imidazo[4,5-e]pyridin-4-amine of Formula XLIII.
• the oxidation reaction is carried out at a reduced temperature, for example, about 0 °C.
• the product or a pharmaceutically acceptable salt thereof can be isolated using conventional methods.
• a 4-phenoxy-lH-imidazo[4,5-c]pyridin-4-amine of Formula XLIII is aminated as in step (8) to provide a lH-imidazo[4,5-c]pyridin-4- amine of Formula XVIII which is a subgenus of Formula 1-6.
• the product or a pharmaceutically acceptable salt thereof can be isolated using conventional methods.
• Some embodiments of the invention including compounds of Formula I-l, 1-2, 1-3, and intermediate compounds can be prepared according to Reaction Scheme II where R , 2, 3 (R M , R-- 2 , and R 1-3 ), R 2 , R 3 , I- , R , R 9 and X are as defined above and BOC is tert- butoxycarbonyl.
• step (1) of Reaction Scheme II the amino group of an aminoalcohol of Formula XIX is protected with a tert-butoxycarbonyl group to provide a compound of Formula XX.
• a solution of the aminoalcohol in tetrahydrofuran is treated with di-tert-butyl dicarbonate in the presence of a base such as sodium hydroxide.
• a base such as sodium hydroxide.
• Many aminoalcohols of Formula XIX are commercially available; others can be prepared using known synthetic methods.
• step (2) of Reaction Scheme II a protected amino alcohol of Formula XX is converted to a methanesulfonate of Formula XXI.
• a solution of a compound of Formula XX in a suitable solvent such as dichloromethane is treated with methanesulfonyl chloride in the presence of a base such as triethylamine.
• the reaction can be carried out at a reduced temperature (0°C).
• step (3 a) of Reaction Scheme II a methanesulfonate of Formula XXI is converted to an azide of Formula XXII.
• Sodium azide is added to a solution of a compound of Formula XXI in a suitable solvent such as N,N-dimethylformamide.
• the reaction can be carried out at an elevated temperature (80 - 100°C).
• step (3b) of Reaction Scheme II a compound of Formula XXII is alkylated with a halide of Formula Hal-R 9 to provide a compound of Formula XXIII.
• R 9 is hydrogen
• this step is omitted.
• the compound of Formula XXII is reacted with sodium hydride in a suitable solvent such as N,N-dimethylformamide to form the anion and then combined with the halide.
• the reaction can be carried out at ambient temperature.
• step (4) of Reaction Scheme II an azide of Formula XXIII is reduced to provide an amine of Formula XXIV.
• the reduction is carried out using a conventional heterogeneous hydrogenation catalyst such as palladium on carbon.
• the reaction can conveniently be carried out on a Parr apparatus in a suitable solvent such as toluene.
• step (5) of Reaction Scheme II a 2,4-dichloro-3-nitropyridine of Formula XI (see Reaction Scheme I) is reacted with an amine of Formula XXIV to provide a 2-chloro- 3-nitropyridine of Formula XXV.
• the reaction can be carried out by adding an amine of Formula XXIV to a solution of a compound of Formula XI in a suitable solvent such as N,N-dimethylformamide in the presence of abase such as triethylamine.
• step (6) of Reaction Scheme II a 2-chloro-3-nitropyridine of Formula XXV is reacted with sodium phenoxide to provide a 3-nifro ⁇ 2-phenoxypyridine of Formula XXVI. Phenol is reacted with sodium hydride in a suitable solvent such as tetiahydrofuran to form the phenoxide. The phenoxide is then reacted at an elevated temperature with a compound of Formula XXV.
• a 3-nitro-2-phenoxypyridine of Formula XXVI is reduced to provide a 2-phenoxypyridine-3,4-diamine of Formula XXVII.
• the reduction is carried out using a conventional heterogeneous catalyst such as platinum on carbon.
• the reaction can be conveniently carried out on a Parr apparatus in a suitable solvent such as, for example, toluene, 2-propanol, ethanol, and mixtures thereof.
• Ni 2 B can be generated in situ from sodium borohydride and NiCl 2 in the presence of methanol.
• a compound of Formula XXVI can be added to the resulting reducing agent solution to effect reduction of the nitro group.
• the Ni 2 B reducing agent can be used without reducing these moieties.
• the product can be isolated from the reaction mixture using conventional methods.
• step (8) of Reaction Scheme II a 2-phenoxypyridine-3, 4-diamine of Formula XXVII is reacted with a carboxylic acid or an equivalent thereof to provide a 4-phenoxy- lH-imidazo[4,5-c]pyridine of Formula XXVIII.
• Suitable equivalents to a carboxylic acid include orthoesters, and 1,1-dialkoxyalkyl alkanoates.
• the carboxylic acid or equivalent is selected such that it will provide the desired R 2 substituent in a compound of Formula XXVIII.
• triethyl orthoformate will provide a compound where R 2 is hydrogen and trimethyl orthovalerate will provide a compound where R 2 is butyl.
• the reaction can be run in the absence of solvent or in an inert solvent such as toluene.
• the reaction is run with sufficient heating to drive off any alcohol or water formed as a byproduct of the reaction.
• a catalyst such as pyridine hydrochloride can be included.
• step (8) can be carried out by (i) reacting the diamine of Formula XXVII with an acyl halide of Formula R 2 C(O)Cl or R 2 C(O)Br and then (ii) cyclizing.
• the acyl halide is added to a solution of the diamine in a suitable solvent such as pyridine.
• the reaction can be carried out at ambient temperature.
• the product of part (i) is heated in pyridine in the presence of pyridine hydrochloride.
• a 4-phenoxy-lH-imidazo[4,5-c]pyridine of Formula XXVIII is aminated to provide a (4-amino-lH-imidazo[4,5- c]pyridinyl)acetamide of Formula VI.
• the reaction can be carried out by combining a compound of Formula XXVIII with ammonium acetate and heating (140 - 160°C).
• the reaction can be carried out in a pressure vessel.
• step (10) of Reaction Scheme II (4-amino-lH-imidazo[4,5- c]pyridinyl)acetamide of Formula VI is hydrolyzed under acidic conditions to provide a lH-imidazo[4,5-c]pyridin-4-amine of Formula II.
• a compound of Formula VI is treated with hydrochloric acid/ethanol at an elevated temperature.
• step (11) of Reaction Scheme II a lH-imidazo[4,5-c]pyridin-4-- ⁇ mine of
• Formula II is converted to a lH-imidazo[4,5-c]pyridin-4-amine of Formula 1-2 using conventional methods.
• sulfonamides of Formula 1-2 can be prepared by reacting a compound of Formula II with a sulfonyl chloride of Formula R a S(O 2 )Cl, where R a is R 8 -alkyl, R 8 -alkenyl, R 8 -aryl, R 8 -heteroaryl or R 8 -heterocyclyl.
• the reaction can be carried out by adding the sulfonyl chloride to a solution of a compound of Formula II in a suitable solvent such as chloroform at ambient temperature.
• Sulfamides of Formula 1-2 can be prepared by reacting a compound of Formula II with sulfiiryl chloride to generate a sulfamoyl chloride in situ and then reacting the sulfamoyl chloride with an amine of Formula ⁇ NRsRa-
• the product or a pharmaceutically acceptable salt thereof can be isolated using conventional methods.
• Amides of Formula I-l can be prepared from lH-imidazo[4,5-c]pyridin-4-amines of Formula II using conventional methods.
• a compound of Formula II can be reacted with an acid chloride of Formula R a C(O)Cl.
• the reaction can be carried out by adding the acid chloride to a solution of a compound of Formula II in a suitable solvent such as chloroform, optionally in the presence of a base such as triethylamine, at ambient temperature.
• a suitable solvent such as chloroform
• a base such as triethylamine
• Ureas and thioureas of Formula 1-3 can be prepared from lH-imidazo[4,5- c]pyridin-4-amines of Formula II using conventional methods.
• a compound of Formula II can be reacted with an isocyanate of Formula RaN ⁇ C ).
• the reaction can be carried out by adding the isocyanate to a solution of a compound of Formula II in a suitable solvent such as chloroform, optionally in the presence of a base such as triethylamine, at ambient temperature.
• the product or a pharmaceutically acceptable salt thereof can be isolated using conventional methods.
• the reaction can be carried out by adding the amine to a solution of compound of Formula XI in a suitable solvent such as N, N- dimethylformamide in the presence of triethylamine.
• a suitable solvent such as N, N- dimethylformamide
• the product of the reaction can be isolated from the reaction mixture using conventional methods.
• Many amines of the formula R 1 - 4 -O-X-NH 2 or R 1-5 -O-X-NH 2 are commercially available; others can be readily prepared using known synthetic methods.
• benzyloxyethylamine hydrochloride can be prepared by reacting tert-butyl 2-(hydroxy)ethylcarbamate with benzyl bromide in the presence of sodium hydroxide and benzyltrimethylammom ' um chloride, and then converting the resulting tert-butyl 2-(benzyloxy)ethylcarbamate to benzyloxyethylamine hydrochloride in the presence of hydrochloric acid, ethanol, and water.
• 2-(3-pyridin-3-yl-propoxy)ethylamine and 2-[3-(l,3-thiazol-2- yl)propoxy]ethylamine can be prepared by reacting tert-butyl 2-(hydroxy)ethylcarbamate with 3-bromopropyne under the phase transfer conditions described above.
• the resulting tert-butyl 2-(prop-2-ynyloxy)ethylcarbamate can be coupled with heteroaryl bromides such as 3-bromopyridine and 2-bromothiazole by means of a palladium complex generated from a palladium catalyst such as dichlorobis(triphenylphosphine)palladium (II) in the presence of copper (I) iodide and a base such as triethylamine.
• a palladium catalyst such as dichlorobis(triphenylphosphine)palladium (II)
• copper (I) iodide and a base such as triethylamine.
• the reaction is conveniently carried out in a suitable solvent such as acetonitrile and can be heated at an elevated temperature.
• the products from the coupling reaction can be hydrogenated in the presence of a conventional heterogeneous catalyst such as 10% palladium on carbon.
• step (2) of Reaction Scheme III a 2-chloro-3-nitropyridine of Formula XXIX-4 or XXIX-5 is reacted with sodium phenoxide to provide a 3-nitro-2-phenoxypyridine of Formula XXX-4 or XXX-5.
• Phenol is reacted with sodium hydride in a suitable solvent such as diglyme (bis(2-methoxyethyl) ether) to form the phenoxide.
• the phenoxide is then reacted at an elevated temperature with a compound of Formula XXIX-4 or XXIX-5.
• the product can be isolated from the reaction mixture using conventional methods.
• step (3) of Reaction Scheme III a 3-nitro-2-phenoxypyridine of Formula XXX- 4 or XXX-5 is reduced to provide a 2-phenoxypyridine-3,4-diamine of Formula XXXI-4 or XXXI-5.
• the reduction is carried out using a conventional heterogeneous catalyst such as platinum on carbon.
• the reaction can be conveniently carried out on a Parr apparatus in a suitable solvent such as toluene.
• Ni 2 B can be generated in situ from sodium borohydride and iC in the presence of methanol.
• a compound of Formula XXX-4 or XXX-5 can be added to the resulting reducing agent solution to effect reduction of the nitro group.
• the M 2 B reducing agent can be used without reducing these moieties.
• the product can be isolated from the reaction mixture using conventional methods.
• step (4) of Reaction Scheme III a 2-phenoxypyridine-3,4-diamine of Formula XXXI-4 or XXXI-5 is reacted with a carboxylic acid or an equivalent thereof to provide a 4-phenoxy-lH-imidazo[4,5-c] ⁇ yridine of Formula XXXII-4 or XXXII-5.
• Suitable equivalents to a carboxylic acid include orthoesters, 1,1-dialkoxyalkyl alkanoates, corresponding acyl halides, and mixtures thereof.
• the carboxylic acid or equivalent is selected such that it will provide the desired R 2 substituent in a compound of Formula XXXII-4 or XXII-5.
• step (4) can be carried out by (i) reacting the diamine of Formula
• acyl halide of Formula R 2 C(O)Cl or R 2 C(O)Br an acyl halide of Formula R 2 C(O)Cl or R 2 C(O)Br and then (ii) cyclizing.
• the acyl halide is added to a solution of the diamine in a suitable solvent such as pyridine.
• the reaction can be carried out at ambient temperature.
• the product of part (i) is heated in pyridine in the presence of pyridine hydrochloride.
• the product can be isolated from the reaction mixture using conventional methods.
• a 4-phenoxy-lH-imidazo[4,5-c] ⁇ yridine of Formula XXXII-4 or XXXII-5 is aminated to provide a lH-imidazo[4,5-c]pyridin-4-amine of Formula 1-4 or 1-5.
• the reaction can be carried out by combining a compound of Formula XXXII-4 or XXXII-5 with ammonium acetate and heating (140 - 160°C).
• the reaction can be carried out in a pressure vessel.
• the product or a pharmaceutically acceptable salt thereof can be isolated using conventional methods.
• Some embodiments of the invention including compounds of Formula I-l and intermediate compounds can be prepared according to Reaction Scheme IV where R M , R 2 , R 3 , R J , X, and Ph are as defined above, and Ac is acetyl.
• a 3-nitro-2-phenoxypyridine of Formula XIII is esterified to provide a 3-nitro-2-phenoxypyridine acetate of Formula XXXIII.
• the esterif ⁇ cation is carried out using acetic anhydride in suitable solvents such as anhydrous dichloromethane and pyridine.
• suitable solvents such as anhydrous dichloromethane and pyridine.
• the product can be isolated from the reaction mixture using conventional methods.
• step (2) of Reaction Scheme TV 3-nitro-2-phenoxypyridine acetate of Formula
• XXXIII is reduced to provide a 2-phenoxypyridine-3,4-diamine Formula XXXIV.
• the reduction is carried out using a conventional heterogeneous catalyst such as platinum on carbon.
• the reaction can be conveniently carried out on a Parr apparatus in a suitable solvent such as toluene.
• Ni 2 B can be generated in situ from sodium borohydride and NiCl 2 in the presence of methanol.
• a compound of Formula XXXIII can be added to the resulting reducing agent solution to effect reduction of the nitro group.
• the Ni 2 B reducing agent can be used without reducing these moieties.
• the product can be isolated from the reaction mixture using conventional methods.
• XXXIV is reacted with a carboxylic acid or an equivalent thereof to provide a 4-phenoxy- lH-imidazo[4,5-e]pyridine of Formula XXXV.
• Suitable equivalents to a carboxylic acid include orthoesters, 1,1-dialkoxyalkyl alkanoates, corresponding acyl halides, and mixtures thereof.
• the carboxylic acid or equivalent is selected such that it will provide the desired R 2 substituent in a compound of Formula XXXV.
• triethyl orthoformate will provide a compound where R 2 is hydrogen and trimethyl orthovalerate will provide a compound where R 2 is butyl.
• the reaction can be run in the absence of solvent or in an inert solvent such as toluene.
• the reaction is run with sufficient heating to drive off any alcohol or water formed as a byproduct of the reaction.
• a catalyst such as pyridine hydrochloride can be included.
• step (3) can be carried out by (i) reacting the diamine of Formula XXXIV with an acyl halide of Formula R 2 C(O)Cl or R 2 C(O)Br and then (ii) cyclizing.
• the acyl halide is added to a solution of the diamine in a suitable solvent such as pyridine.
• the reaction can be carried out at ambient temperature.
• the product of part (i) is heated in pyridine in the presence of pyridine hydrochloride.
• the product can be isolated from the reaction mixture using conventional methods.
• step (4) of Reaction Scheme TV a 4-phenoxy-lH-imidazo[4,5-c]pyridine acetate of Formula XXXV is hydrolyzed to provide a 4-phenoxy-lH-imidazo[4,5-c]pyridine alcohol of Formula XXXVI.
• the reaction is preferably carried out in methanol in the presence of potassium carbonate at an elevated temperature.
• the product can be isolated from the reaction mixture using conventional methods.
• step (5) of Reaction Scheme TV a 4-phenoxy-lH-imidazo[4,5-c]pyridine alcohol of Formula XXXVI is reacted with a compound of formula ⁇ alo-R 1- to provide a 4-phenoxy-lH-imidazo[4,5-c]pyridine of Formula XXXII-4.
• the reaction can be carried out by first reacting the alcohol of Formula XXXVI with sodium hydride in a suitable solvent such as N,N-dimethylformamide to form the corresponding anion and then reacting the anion with a compound of formula ⁇ alo-R 1-4 .
• the product can be isolated from the reaction mixture using conventional methods.
• step (6) of Reaction Scheme TV a 4-phenoxy-lH-imidazo[4,5-c]pyridine of
• Formula XXXII-4 is aminated to provide a lH-imidazo[4,5-c]pyridin-4-amine of Formula 1-4.
• the reaction can be carried out by combining a compound of Formula XXXII-4 with ammonium acetate and heating (140 - 160°C).
• the reaction can be carried out in a pressure vessel.
• the product or a pharmaceutically acceptable salt thereof can be isolated using conventional methods.
• Some embodiments of the invention including compounds of Formula XXXIX and intermediate compounds can be prepared according to Reaction Scheme V where R 2 , R 3 , R 4 , X, and Ph are as defined above, and R 13 is aryl, substituted aryl, heteroaryl, or substituted heteroaryl.
• step (1) of Reaction Scheme V the alkyne bond of a 4-phenoxy-lH- imidazo[4,5-c]pyridine of Formula XXXVII, which is a subgenus of Formula XXXII-4 or XXXII-5, is reduced to form a 4-phenoxy-lH-imidazo[4,5-c]pyridine of Formula XXXVm, which is also a subgenus of Formula XXXII-4 or XXXII-5.
• the reduction is carried out using a conventional heterogeneous catalyst such as platinum oxide, platinum on carbon, or palladium on carbon.
• the reaction can conveniently be carried out on a Parr apparatus in a suitable solvent such as methanol.
• the product can be isolated from the reaction mixture using conventional methods.
• a 4-phenoxy-lH-imidazo[4,5-c]pyridine of Formula XXXVIII is aminated to provide a lH-imidazo[4,5-c]pyridin-4-amine of Formula XXXIX, which a subgenus of Formula 1-4 or 1-5.
• the reaction can be carried out by combining a compound of Formula XXXVIII with ammonium acetate and heating (140 - 160°C).
• the reaction can be carried out in a pressure vessel.
• the product or a pharmaceutically acceptable salt thereof can be isolated using conventional methods.
• Ri- 4 , R 2 , R 3 , R., X, and Ph are as defined above.
• step (1) of Reaction Scheme VI a 2-chloro-3-nitropyridine of Formula XXIX-4, prepared as described in Reaction Scheme III, is reduced to provide a 2-chloropyridine- 3,4-diamine of Formula XL.
• the reduction is carried out using a conventional heterogeneous catalyst such as platinum on carbon or palladium on carbon.
• the reaction can be conveniently carried out on a Parr apparatus in a suitable solvent such as toluene.
• Ni 2 B can be generated in situ from sodium borohydride and NiCl 2 in the presence of methanol.
• a compound of Formula XXIX-4 can be added to the resulting reducing agent solution to effect reduction of the nitro group.
• the Ni 2 B reducing agent can be used without reducing these moieties.
• the product can be isolated from the reaction mixture using conventional methods.
• a 2-chloropyridine-3,4-diamine of Formula XL is reacted with a carboxylic acid or an equivalent thereof to provide a 4-chloro-lH- imidazo[4,5-c]pyridine of Formula XLII.
• Suitable equivalents to a carboxylic acid include orthoesters, 1,1-dialkoxyalkyl alkanoates, corresponding acyl halides, and mixtures thereof.
• the carboxylic acid or equivalent is selected such that it will provide the desired R 2 substituent in a compound of Formula XLII. For example, triethyl orthoformate will provide a compound where R 2 is hydrogen and trimethyl orthovalerate will provide a compound where R 2 is butyl.
• the reaction can be run in the absence of solvent or in an inert solvent such as toluene.
• the reaction is run with sufficient heating to drive off any alcohol or water formed as a byproduct of the reaction.
• a catalyst such as pyridine hydrochloride can be included.
• step (2) can be carried out by (2a) reacting the diamine of Formula XL with an acyl halide of Formula R 2 C(O)Cl or R 2 C(O)Br and then (2b) cyclizing.
• the acyl halide is added to a solution of the diamine of Formula XL in an inert solvent such as dichloromethane or acetonitrile.
• the reaction can be carried out at ambient temperature.
• a tertiary amine for example triethylamine, is included, hi part (2b), the product of part (2a), a compound of Formula XLI, is heated at reflux in a suitable solvent such as ethanol in the presence of triethylamine.
• the product can be isolated from the reaction mixture using conventional methods.
• step (3) of Reaction Scheme VI a 4-chloro-lH-imidazo[4,5-c]pyridine of Formula XLII is reacted with sodium phenoxide to provide a 4-phenoxy-lH-imidazo[4,5- c]pyridine of Formula XXXII-4.
• Phenol is reacted with sodium hydride in a suitable solvent such as diglyme (bis(2-methoxyethyl) ether) to form the phenoxide.
• the phenoxide is then reacted at an elevated temperature with a compound of Formula XLII.
• the product can be isolated from the reaction mixture using conventional methods.
• a 4-phenoxy-lH-imidazo[4,5-c]pyridine of Formula XXXII-4 is aminated to provide a lH-imidazo[4,5-c]pyridin-4-amine of Formula 1-4.
• the reaction can be carried out by combining a compound of Formula XXXII-4 with ammonium acetate and heating (140 - 160°C).
• the reaction can be carried out in a pressure vessel.
• the product or a pharmaceutically acceptable salt thereof can be isolated using conventional methods.
• Some embodiments of the invention including compounds of Formulas XLV-1, XLV-2, XLV-3, XLVI-1, XLVI-2, XLVI-3, and intermediate compounds can be prepared according to Reaction Scheme VII where R .2, 3 (R , R1-2- R1-3)-. R2-. Re, R9, and X are as defined above, R ⁇ is -Br or -NO2, and ⁇ is C2-!o alkynyl and C M O alkyl.
• step (1) of Reaction Scheme VII bromination or nitration of a (4-amino-lH- imidazo[4,5-c]pyridinyl)acetamide of Formula Via provides a (7-substituted)-(4-amino- lH-imidazo[4,5-c]pyridinyl)acetamide of Formula XLIV.
• the bromination reaction can be carried out by treating the acetamide of Formula Via in a solution of acetic acid with bromine and potassium acetate at ambient temperature.
• the direct nitration reaction can be carried out by treating the acetamide of Formula Via with one equivalent of nitric acid in the presence of excess acetic acid and heating the reaction, optionally, at reflux.
• step (2) of Reaction Scheme VII a (7-substituted)-(4-amino-lH-imidazo[4,5- c]pyridinyl)acetamide of Formula XLIV is hydrolyzed under acidic conditions to provide a (7-substituted)-lH-imidazo[4,5-c]pyridin-4-amine of Formula Ila, which is a subgenus of compounds of Formula II.
• a compound of Formula XLIV is treated with hydrochloric acid/ethanol at an elevated temperature, for example, at reflux.
• the product can be isolated using conventional methods.
• step (3) of Reaction Scheme VII a lH-imidazo[4,5-c]pyridin-4-amine of
• Formula Ila is converted to a lH-imidazo[4,5-c]pyridin-4-amine of Formula XLV-1, XLV-2, or XLV-3 using conventional methods.
• Formulas XLV-1, XLV-2, and XLV-3 are subgenera of Formulas I-l, 1-2, and 1-3, respectively.
• sulfonamides of Formula XLV-2 can be prepared by reacting a compound of Formula Ila with a sulfonyl chloride of Formula R a S(O 2 )Cl, where R a is R 8 -alkyl, R 8 -alkenyl, R 8 -aryl, R 8 -heteroaryl or Rs-heterocyclyl.
• the reaction can be carried out by adding the sulfonyl chloride to a solution of a compound of Formula Ila in a suitable solvent such as chloroform at ambient temperature.
• Sulfamides of Formula XLV-2 can be prepared by reacting a compound of Formula Ila with sulfuryl chloride to generate a sulfamoyl chloride in situ, and then reacting the sulfamoyl chloride with an amine of Formula HNRsR a .
• the product or a pharmaceutically acceptable salt thereof can be isolated using conventional methods.
• Amides of Formula XLV-1 can be prepared from lH-imidazo[4,5-c]pyridin-4- amines of Formula Ila using conventional methods.
• a compound of Formula Ila can be reacted with an acid chloride of Formula R a C(O)Cl, where R a is R 8 -alkyl, R 8 - alkenyl, R 8 -aryl, R 8 -heteroaryl or R 8 -heterocyclyl.
• the reaction can be carried out by adding the acid chloride to a solution of a compound of Formula Ila in a suitable solvent such as chloroform, optionally in the presence of a base such as triethylamine, at ambient temperature.
• Ureas and thioureas of Formula XLV-3 can be prepared from lH-imidazo[4,5- c]pyridin-4-amines of Formula Ila using conventional methods.
• the reaction can be carried out by adding the isocyanate to a solution of a compound of Formula Ila in a suitable solvent such as chloroform, optionally in the presence of a base such as triethylamine, at ambient temperature.
• the product or a pharmaceutically acceptable salt thereof can be isolated using conventional methods.
• step (4) of Reaction Scheme VH a lH-imidazo[4,5-c]pyridin-4-amine of Formula XLV-1, XLV-2, or XLV-3 undergoes a coupling reaction with a C 2 -10 alkyne, conveniently by means of a palladium complex to provide a lH-imidazo[4,5-c]pyridin-4- a ine of Formula XLVI-1, XLVI-2, or XLVI-3, which are subgenera of Formulas I-l, 1-2, and 1-3, respectively.
• the alkyne is added to a solution of a compound of Formula XLV- 1, XLV-2, or XLV-3 in a suitable solvent such as acetonitrile in the presence of a palladium catalyst, for example, dichlorobis(triphenylphosphine)palladium (II), copper (I) iodide, and a base such as triethylamine.
• a palladium catalyst for example, dichlorobis(triphenylphosphine)palladium (II), copper (I) iodide, and a base such as triethylamine.
• the reaction can be heated at an elevated temperature.
• R ⁇ is C 2 - 10 alkynyl
• reduction as described in step (1) of Reaction Scheme V can be used to convert u, to C 2 -10 alkyl.
• the product or a pharmaceutically acceptable salt thereof can be isolated using conventional methods.
• Some embodiments of the invention including compounds of Formula XVIII and intermediate compounds can be prepared according to Reaction Scheme VIII where R 2 , R 3 , R . , and X are as defined above.
• step (1) of Reaction Scheme VIII a 2-chloro-3-nitro ⁇ yridine of Formula XII is reacted with an alkali metal azide to provide an 8-nitrotetrazolo[l,5- ⁇ ]pyridine of Formula XLVII.
• the reaction can be carried out by combining the compound of Formula XII with an alkali metal azide, for example, sodium azide, in a suitable solvent such as anhydrous NN-dimethylformamide, and heating to about 50 - 100 °C, optionally in the presence of ammonium chloride.
• the reaction can be carried out by combining the compound of Formula XII with an alkali metal azide, for example, sodium azide, in a suitable solvent such as 90/10 acetonitrile/H 2 ⁇ in the presence of cerium III chloride, preferably cerium III chloride heptahydrate, optionally with heating, for example, at reflux.
• cerium III chloride preferably cerium III chloride heptahydrate
• the product can be isolated from the reaction mixture using conventional methods.
• an 8-nitrotetrazolo[l,5- ⁇ ]pyridine of Formula XLVII is chlorinated using conventional chlorinating agents to provide an 8- nitrotetrazolo[l,5- ]pyridine of Formula XLVIII.
• the reaction is carried out by combining a compound of Formula XLVII with thionyl chloride in a suitable solvent such as dichloromethane and heating.
• step (3) of Reaction Scheme VIII an 8-nitrotetrazolo[l,5- ]pyridine of Formula XLVIII is reduced to provide a tetrazolo[l ,5- ⁇ ]pyridine-7,8-diamine of Formula XLIX.
• the reduction is carried out using a conventional heterogeneous catalyst such as platinum on carbon.
• the reaction can be conveniently carried out on a Parr apparatus in a suitable solvent such as toluene.
• M 2 B can be generated in situ from sodium borohydride and MCI 2 in the presence of methanol.
• a compound of Formula XLVIII can be added to the resulting reducing agent solution to effect reduction of the nitro group.
• the ⁇ i 2 B reducing agent can be used without reducing these moieties.
• the product can be isolated from the reaction mixture using conventional methods.
• step (4) of Reaction Scheme VIII a tetrazolo[l,5- ⁇ ]pyridine-7,8-diamine of
• Formula XLIX is reacted with a carboxylic acid or an equivalent thereof to provide a 7H- imidazo[4,5-c]tetrazolo[l,5- ⁇ ]pyridine of Formula L.
• Suitable equivalents to a carboxylic acid include, for example, orthoesters, and 1,1-dialkoxyalkyl alkanoates.
• the carboxylic acid or equivalent is selected such that it will provide the desired R 2 substituent in a compound of Formula L.
• triethyl orthoformate will provide a compound where R 2 is hydrogen, and trimethyl orthovalerate will provide a compound where R2 is butyl.
• the reaction can be run in the absence of solvent or in an inert solvent such as toluene.
• the reaction is run with sufficient heating to drive off any alcohol or water formed as a byproduct of the reaction.
• a catalyst such as pyridine hydrochloride can be included.
• step (4) can be carried out by (i) reacting the diamine of Formula XLIX with an acyl halide of Formula R 2 C(O)Cl or R 2 C(O)Br and then (ii) cyclizing.
• the acyl halide is added to a solution of the diamine in a suitable solvent such as pyridine.
• the reaction can be carried out at ambient temperature.
• the product of part (i) is heated in pyridine in the presence of pyridine hydrochloride.
• a 7H-imidazo[4,5-c]tetrazolo[l,5- ]pyridine of Formula L is reacted with a compound of Formula R ⁇ ⁇ SNa to provide a 7H- imidazo[4,5-c]tetrazolo[l,5- ⁇ ]pyridine of Formula LI.
• a thiol of the Formula R ⁇ - ⁇ S ⁇ is reacted with sodium hydride in a suitable solvent such as N,N- dimethylformamide to generate the anion, which is then reacted with a compound of Formula L.
• a 7H-imidazo[4,5-c]tetrazolo[l,5- ]pyridine of Formula LI is oxidized to provide a 7H-imidazo[4,5-c]tetrazolo[l,5- ⁇ ]pyridine of Formula LII.
• a solution of a compound of Formula LI in a suitable solvent such as chloroform or dichloromethane is treated with 3-chloroperoxybenzoic acid.
• the degree of oxidation is controlled by adjusting the amount of 3-chloroperoxybenxzoic acid used in the reaction; i.e., using approximately one equivalent will provide the sulfoxide whereas using two equivalents will provide the sulfone.
• the product can be isolated using conventional methods.
• step (7) of Reaction Scheme VIII a 7H-imidazo[4,5-c]tetrazolo[l,5- ]pyridine of Formula LII is reacted with triphenylphosphine to form an N-triphenylphosphinyl compound of Formula LIII.
• the reaction with triphenylphosphine can be run in a suitable solvent such as toluene or 1,2-dichlorobenzene under an atmosphere of nitrogen with heating, for example at the reflux temperature.
• step (8) of Reaction Scheme VIII an N-triphenylphosphinyl compound of Formula LIII is hydrolyzed to provide a lH-imidazo[4,5-e]pyridin-4-amine of Formula XVIII, which is a subgenus of Formula 1-6.
• the hydrolysis can be carried out by general methods well known to those skilled in the art, for example, by heating in a lower alkanol in the presence of an inorganic acid, such as hydrochloric acid.
• the product can be isolated from the reaction mixture using conventional methods as the compound of Formula XVIII or as a pharmaceutically acceptable salt thereof.
• steps (7) and (8) of Reaction Scheme Vffl can be omitted, and the tetrazolo ring can be reductively removed from a 7H-imidazo[4,5-c]tetrazolo[l,5- ⁇ ]pyridine of Formula LII to provide a lH-imidazo[4,5-c]pyridin-4-amine of Formula XVIII.
• the reaction can be carried out by reacting the 7H-imidazo[4,5-c]tetrazolo[l,5- ⁇ ] ⁇ yridine of Formula LII with hydrogen in the presence of an catalyst and an acid.
• the reaction can be conveniently run in a Parr apparatus with a suitable catalyst, such as platinum IV oxide, and a suitable acid, such as trifluoroacetic acid or concentrated hydrochloric acid.
• the product can be isolated from the reaction mixture using conventional methods.
• Some embodiments of the invention including compounds of Formula XVIIIa and intermediate compounds can be prepared according to Reaction Scheme IX where R 2 , R 3 , R t , and X are as defined above, R' and R" are independently hydrogen or C MO alkyl, and Et is ethyl.
• step (1) of Reaction Scheme IX a 7H-imidazo[4,5-c]tetrazolo[l,5- ⁇ ]pyridine of Formula Llla, which is a subgenus of Formula LII, is hydrolyzed to provide a 7H- imidazo[4,5-c]tetrazolo[l,5- ]pyridine of Formula Lllb.
• the reaction can be carried out under conventional saponification conditions by treating the ester with aqueous sodium hydroxide in a suitable solvent or solvent mixture such as tefrahydrofuran/methanol.
• a suitable solvent or solvent mixture such as tefrahydrofuran/methanol.
• reaction can be optionally carried out with heating.
• the reaction mixture is acidified in a subsequent step by stirring with, for example, hydrochloric acid to provide the carboxylic acid.
• step (2) of Reaction Scheme IX a 7H-imidazo[4,5-c]tet ⁇ azolo[l,5- ⁇ ]pyridine of Formula Lllb, which is a subgenus of Formula LII, is converted to a 7H-imidazo[4,5- c]tetrazolo[l,5- ]pyridine acid chloride of Formula LTV.
• the reaction can be carried out by combining a compound of Formula Lllb with oxalyl chloride or thionyl chloride in a suitable solvent such as dichloromethane and, optionally, heating.
• step (3) of Reaction Scheme IX a 7H-imidazo[4,5-c]tetrazolo[l,5- ⁇ ]pyridine acid chloride of Formula LTV is converted to a 7H-imidazo[4,5-c]tetrazolo[l,5- ⁇ ]pyridine amide of Formula LIIc, which is a subgenus of Formula LII.
• the reaction can be carried out by combining a compound of Formula LTV with an amine in a suitable solvent such as dichloromethane and stirring at ambient temperature.
• step (4) of Reaction Scheme IX a 7H-imidazo[4,5-c]tetrazolo[l,5- ]pyridine amide of Formula LIIc is reacted with triphenylphosphine to form an N- triphenylphosphinyl compound of Formula LUIa, which is a subgenus of Formula LIII.
• the reaction with triphenylphosphine can be run in a suitable solvent such as toluene or 1,2-dichlorobenzene under an atmosphere of nitrogen with heating, for example at the reflux temperature.
• a suitable solvent such as toluene or 1,2-dichlorobenzene
• LUIa is hydrolyzed to provide a lH-imidazo[4,5-c]pyridin-4-amine of Formula XVIIIa, which is a subgenus of Formula XVIII, which in turn is a subgenus of Formula 1-6.
• the hydrolysis can be carried out by general methods well known to those skilled in the art, for example, by heating in a lower alkanol in the presence of an inorganic acid, such as hydrochloric acid.
• the product can be isolated from the reaction mixture using conventional methods as the compound of Formula XVIIIa or as a pharmaceutically acceptable salt thereof.
• steps (4) and (5) of Reaction Scheme IX can be omitted, and the tetrazolo ring can be reductively removed from a 7H-imidazo[4,5-c]tetrazolo[l,5- ⁇ ]pyridine amide of Formula LIIc to provide a lH-imidazo[4,5-c]pyridin-4-amine of Formula XVIIIa.
• the reaction can be carried out by reacting the 7H-imidazo[4,5- c]tetrazolo[l,5- ]pyridine amide of Formula LIIc with hydrogen in the presence of an catalyst and an acid.
• the reaction can be conveniently run in a Parr apparatus with a suitable catalyst, such as platinum IV oxide, and a suitable acid, such as trifluoroacetic acid or concentrated hydrochloric acid.
• the product can be isolated from the reaction mixture using conventional methods.
• step (1) of Reaction Scheme X a 2-chloro-3-nitropyridine of Formula XXV is reacted with an alkali metal azide to provide an 8-nitrotetrazolo[l,5-a]pyridine of Formula LV.
• the reaction can be carried out as described in step (1) of Reaction Scheme VIII.
• the product can be isolated from the reaction mixture using conventional methods.
• step (2) of Reaction Scheme X an 8-nitrotetrazolo[l,5- ⁇ ]pyridine of Formula LV is reduced to provide a tet ⁇ azolo[l,5- ]pyridine-7,8-diamine of Formula LVI.
• the reduction can be carried out as described in step (3) of Reaction Scheme VIII.
• step (3) of Reaction Scheme X a tetrazolo[l,5- ⁇ ]pyridine-7,8-diamine of Formula LVI is reacted with a carboxylic acid or an equivalent thereof to provide a 7H- imidazo[4,5-c]tetrazolo[l,5- ⁇ ]pyridine of Formula LVII.
• the reaction can be carried out as described in step (4) of Reaction Scheme VIII.
• step (4) of Reaction Scheme X the BOC group of a 7H-imidazo[4,5- c]tetrazolo[l,5- ⁇ ]pyridine of Formula LVII is removed to provide a 7H-imidazo[4,5- c]tetrazolo[l,5- ⁇ ]pyridine of Formula LVIII.
• the reaction can be carried out by treating a solution of a 7H-imidazo[4,5-c]tetrazolo[l,5- ⁇ ]pyridine of Formula LVII in a suitable solvent such as, for example, dichloromethane with an acid, preferably trifluoroacetic acid, at ambient temperature.
• the product can be isolated from the reaction mixture using conventional methods.
• step (5) of Reaction Scheme X a 7H-imidazo[4,5-c]tefrazolo[l,5- ⁇ ]pyridine of
• Formula LVIII is converted to a 7H-imidazo[4,5-c]tefrazolo[l,5- ⁇ ]pyridine of Formula LIX-l, LIX-2, or LIX-3 using conventional methods.
• sulfonamides of Formula LIX-2 can be prepared by reacting a compound of Formula LVIII with a sulfonyl chloride of Formula R a S(O 2 )Cl, where R a is R 8 -alkyl, R 8 -alkenyl, R 8 -aryl, R 8 -heteroaryl or R 8 -heterocyclyl.
• the reaction can be carried out by adding the sulfonyl chloride to a solution of a compound of Formula LVIII in a suitable solvent such as chloroform at ambient temperature.
• Sulfamides of Formula LIX-2 can be prepared by reacting a compound of Formula LVIII with sulfuryl chloride to generate a sulfamoyl chloride in situ, and then reacting the sulfamoyl chloride with an amine of Formula ⁇ NRsR a .
• the product or a pharmaceutically acceptable salt thereof can be isolated using conventional methods.
• a 7H-imidazo[4,5-c]tetrazolo[l,5- ⁇ ]pyridine of Formula LVIII is reacted with a chloroalkanesulfonyl chloride of formula Cl-Rn-S ⁇ Cl to provide a subgenus of compounds of Formula LIX-2 wherein R 9 and R ⁇ join to form a ring having the structure
• the reaction is preferably carried out by adding the chloroalkanesulfonyl chloride to a solution of a compound of Formula LVIII in a suitable solvent such as dichloromethane in the presence of a base such as triethylamine.
• a suitable solvent such as dichloromethane
• the intermediate chloroalkanesulfonamide may optionally be isolated before treatment with a stronger base such as 1,8- diazabicyclo[5.4.0]undecene-7 (DBU) at ambient temperature. If the intermediate chloroalkanesulfonamide is isolated, the reaction with DBU can be carried out in a suitable solvent such as N,N-dimethylformamide.
• DBU 1,8- diazabicyclo[5.4.0]undecene-7
• the product or a pharmaceutically acceptable salt thereof can be isolated using conventional methods.
• Amides of Formula LIX-l can be prepared from 7H-imidazo[4,5-c]tetrazolo[l,5- ⁇ j yridine of Formula LVIII using conventional methods.
• a compound of Formula LVIII can be reacted with an acid chloride of Formula RaC(O)Cl where R a is R 8 - alkyl, R 8 -alkenyl, R 8 -aryl, R 8 -heteroaryl or R 8 -heterocyclyl.
• the reaction can be carried out by adding the acid chloride to a solution of a compound of Formula LVIII in a suitable solvent such as chloroform, optionally in the presence of a base such as triethylamine, at ambient temperature.
• the product can be isolated using conventional methods.
• a 7H-imidazo[4,5-c]tetrazolo[l,5- «]pyridine of Formula LVIII is reacted with a chloroalkanoyl chloride compound of formula Cl-Ri2-C(O)Cl to provide a subgenus of compounds of Formula LIX-l wherein R 9 and R 10 join to form a ring having the structure
• the reaction is preferably carried out by adding the chloroalkanoyl chloride compound to a solution of a compound of Formula LVIII in a suitable solvent such as dichloromethane in the presence of a base such as triethylamine.
• a suitable solvent such as dichloromethane
• the intermediate chloroalkanamide may optionally be isolated before treatment with a stronger base such as 1 ,8- diazabicyclo[5.4.0]undecene-7 (DBU) at ambient temperature. If the intermediate chloroalkanamide is isolated, the reaction with DBU can be carried out in a suitable solvent such as N,N-dimethylformamide.
• the product can be isolated using conventional methods.
• Ureas and thioureas of Formula LIX-3 can be prepared from 7H-imidazo[4,5- c]tetrazolo[l,5- ]pyridine of Formula LVIII using conventional methods.
• the reaction can be carried out by adding the isocyanate to a solution of a compound of Formula LVIII in a suitable solvent such as chloroform, optionally in the presence of a base such as triethylamine, at ambient temperature.
• the product can be isolated using conventional methods.
• step (6) of Reaction Scheme X a 7H-imidazo[4,5-c]tetrazolo[l,5- ⁇ ]pyridine of Formula LIX-l, LIX-2, or LIX-3 is reacted with triphenylphosphine to form an N- triphenylphosphinyl compound of Formula LX-1, LX-2, or LX-3.
• the reaction with triphenylphosphine can be run in a suitable solvent such as toluene or 1,2-dichlorobenzene under an atmosphere of nitrogen with heating, for example at the reflux temperature.
• step (7) of Reaction Scheme X an N-triphenylphosphinyl compound of Formula LX-1, LX-2, or LX-3 is hydrolyzed to provide a lH-imidazo[4,5-c]pyridin-4-amine of Formula I-l, 1-2, or 1-3.
• the hydrolysis can be carried out by general methods well known to those skilled in the art, for example, by heating in a lower alkanol in the presence of an inorganic acid such as hydrochloric acid.
• the product can be isolated from the reaction mixture using conventional methods as the compound of Formula I-l, 1-2, or 1-3 or as a pharmaceutically acceptable salt thereof.
• steps (6) and (7) of Reaction Scheme X can be omitted, and the tetrazolo ring can be reductively removed from a 7H-imidazo[4,5-c]tetrazolo[l,5- jpyridine of Formula LIX-l, LIX-2, or LIX-3 to provide a lH-imidazo[4,5-c]pyridin-4- amine of Formula I-l, 1-2, or 1-3.
• the reaction can be carried out by reacting the 7H- imidazo[4,5-c]tetrazolo[l,5- ]pyridine of Formula LIX-l, LIX-2, or LIX-3 with hydrogen in the presence of an catalyst and an acid.
• reaction Scheme X Reaction Scheme X
• Some embodiments of the invention including compounds of Formula 1-4, 1-5, and intermediate compounds can be prepared according to Reaction Scheme XI where R , 5 (R 1- and R 1-5 ), R2, R 3 , t, and X are as defined above.
• h step (1) of Reaction Scheme XI a 2-chloro-3-nitropyridine of Formula XXIX-4 or XXIX-5 is reacted with an alkali metal azide to provide an 8-nitrotetrazolo[l,5- ⁇ ]pyridine of Formula LXII-4 or LXII-5.
• the reaction can be carried out as described in step (1) of Reaction Scheme VIII.
• the product can be isolated from the reaction mixture using conventional methods.
• hi step (2) of Reaction Scheme XI an 8-nitrotetrazolo[l,5- ⁇ ]pyridine of Formula
• LXII-4 or LXII-5 is reduced to provide tetrazolo[l,5- ⁇ ]pyridine-7,8-diamine of Formula LXIII-4 or LXIII-5.
• the reduction can be carried out as described in step (3) of Reaction
• step (3) of Reaction Scheme XI a tetrazolo[l,5- ⁇ ]pyridine-7,8-diamine of
• Formula LXIII-4 or LXIII-5 is reacted with a carboxylic acid or an equivalent thereof to provide a 7H-imidazo[4,5-c]tetrazolo[l,5-a]pyridine of Formula LIX-4 or LIX-5.
• the reaction can be carried out as described in step (4) of Reaction Scheme VIII.
• the product can be isolated from the reaction mixture using conventional methods.
• Formula LIX-4 or LIX-5 is reacted with triphenylphosphine to form an N- triphenylphosphinyl compound of Formula LX-4, or LX-5.
• the reaction can be carried out as described in step (6) of Reaction Scheme X.
• the product can be isolated from the reaction mixture using conventional methods.
• LX-4, or LX-5 is hydrolyzed to provide a lH-imidazo[4,5-c]pyridin-4-amine of Formula 1-4 or 1-5.
• the hydrolysis can be carried out as described in step (7) of Reaction Scheme
• the product can be isolated from the reaction mixture using conventional methods as the compound of Formula 1-4, or 1-5 or as a pharmaceutically acceptable salt thereof.
• steps (4) and (5) of Reaction Scheme XI can be omitted, and the tetrazolo ring can be reductively removed from a 7H-imidazo[4,5-c]tetrazolo[l,5- ⁇ jpyridine of Formula LIX-4 or LIX-5 to provide a lH-imidazo[4,5-c]pyridin-4-amine of
• the reaction can be carried out by reacting the 7H-imidazo[4,5- c]tetrazolo[l,5- ⁇ ]pyridine of Formula LIX-4 or LIX-5 with hydrogen in the presence of an catalyst and an acid.
• the reaction can be conveniently run in a Parr apparatus with a suitable catalyst, such as platinum IV oxide, and a suitable acid, such as trifluoroacetic acid or concentrated hydrochloric acid.
• a suitable catalyst such as platinum IV oxide
• a suitable acid such as trifluoroacetic acid or concentrated hydrochloric acid.
• the product can be isolated from the reaction mixture using conventional methods.
• Some embodiments of the invention including compounds of Formula 1-5 and intermediate compounds can be prepared according to Reaction Scheme XII where Ri-5, R 2 , R 3 , R 4 , X, and Ac are as defined above.
• a 2-chloro-3-nitropyridine of Formula XII is esterified to provide a 2-chloro-3-nitropyridine acetate of Formula LXVI.
• the esterification is carried out using acetic anhydride in a suitable solvent such as anhydrous dichloromethane in the presence of pyridine and catalytic 4-dimethylaminopyridine (DMAP).
• DMAP catalytic 4-dimethylaminopyridine
• step (2) of Reaction Scheme XII a 2-chloro-3-nitropyridine of Formula LXVI is reacted with an alkali metal azide to provide an 8-nitrotetrazolo[l,5-a]pyridine of Formula LXVII.
• the reaction can be carried out as described in step (1) of Reaction Scheme VIII.
• the product can be isolated from the reaction mixture using conventional methods.
• step (3) of Reaction Scheme XII an 8-nitrotetrazolo[l,5- ⁇ ]pyridine of Formula LXVII is reduced to provide tefrazolo[l,5- ⁇ ]pyridine-7,8-diarnine of Formula LXVIII.
• the reduction can be carried out as described in step (3) of Reaction Scheme VIII.
• the product can be isolated from the reaction mixture using conventional methods.
• step (4) of Reaction Scheme XII a tetrazolo [1,5 - ⁇ ]pyridine-7 , 8 -diamine of Formula LXVIII is reacted with a carboxylic acid or an equivalent thereof to provide a 7H-imidazo[4,5-c]tetrazolo[l,5- ]pyridine of Formula LXIX.
• the reaction can be carried out as described in step (4) of Reaction Scheme VIII.
• the product can be isolated from the reaction mixture using conventional methods.
• a 7H-imidazo[4,5-c]tetrazolo[l,5- ⁇ ]pyridine of Formula LXIX is hydrolyzed using conventional methods to provide a 7H-imidazo[4,5- c]tetrazolo[l,5- ⁇ ]pyridine of Formula LXX.
• the reaction can be conveniently carried out by adding potassium carbonate to a 7H-imidazo[4,5- c]tetrazolo[l,5- ⁇ ]pyridine of Formula LXIX dissolved in methanol at an elevated temperature.
• the product can be isolated from the reaction mixture using conventional methods.
• a 7H-imidazo[4,5-c]tetrazolo[l,5- ]pyridine of Formula LXX is reacted with 3-bromopropyne to provide a 7H-imidazo[4,5- c]tetrazolo[l,5- ⁇ ]pyridine of Formula LXXI.
• the reaction can be carried out by adding 3- bromopropyne to 7H-imidazo[4,5-c]tetrazolo[l,5- ⁇ ]pyridine of Formula LXX under phase transfer conditions with catalytic benzyltrimethylammonium chloride in a mixture of a a suitable solvent such as dichloromethane and 50% aqueous sodium hydroxide.
• the product can be isolated from the reaction mixture using conventional methods.
• hi step (7) of Reaction Scheme XII 7H-imidazo[4,5-c]tetrazolo[l,5- ⁇ ]pyridine of Formula LXXI is reacted with a heteroarylbromide or heterocyclylbromide to provide a 7H-imidazo[4,5-c]tetrazolo[l,5- ⁇ ]pyridine of Formula LIX-5.
• the reaction can be carried out by coupling a heteroarylbromide, for example, 5-bromopyrimidine, or heterocyclylbromide with the alkyne group of a 7H-imidazo[4,5-c]tetrazolo[l,5- ⁇ ]pyridine of Formula LXXI.
• the coupling reaction can proceed through a palladium complex, generated from a palladium catalyst, for example --,,-,--_schreib endeavor
• step (8) of Reaction Scheme XII a 7H-imidazo[4,5-c]tetrazolo[l,5- ]pyridine of
• Formula LX-5 is hydrolyzed to provide a lH-imidazo[4,5-c]pyridin-4-amine of Formula I- 5.
• the hydrolysis can be carried out as described in step (7) of Reaction Scheme X.
• the product can be isolated from the reaction mixture using conventional methods as the compound of Formula 1-5 or as a pharmaceutically acceptable salt thereof.
• steps (8) and (9) of Reaction Scheme XII can be omitted, and the tetrazolo ring can be reductively removed from a 7H-imidazo[4,5-c]tetrazolo[l,5- ]pyridine of Formula LIX-5 to provide a lH-imidazo[4,5-c]pyridin-4-amine of Formula 1-5.
• the reaction can be carried out by reacting the 7H-imidazo[4,5-c]tetrazolo[l,5- ⁇ jpyridine of Formula LIX-5 with hydrogen in the presence of an catalyst and an acid.
• the reaction can be conveniently run in a Parr apparatus with a suitable catalyst, such as platinum TV oxide, and a suitable acid, such as trifluoroacetic acid or concentrated hydrochloric acid.
• a suitable catalyst such as platinum TV oxide
• a suitable acid such as trifluoroacetic acid or concentrated hydrochloric acid.
• the product can be isolated from the reaction mixture using conventional methods.
• Some embodiments of the invention including compounds of Formulas LXXVII-1, LXXVII-2, LXXVII-3, and intermediate compounds can be prepared according to Reaction Scheme XIII where R ⁇ -1,2,3 (R1-1, R1-2, and R ), R 2 , R ⁇ , R 9 , X, and BOC are as defined above, Tf is trifluoromethylsulfonyl, and PMB is 4-methoxybenzyl.
• step (1) of Reaction Scheme XIII malonyl dichloride is stirred with propanenitrile at ambient temperature to provide 6-chloro-4-hydroxy-5-methylpyridin- 2(lH)-one hydrochloride hydrate, which precipitates from the solution.
• step (2) of Reaction Scheme XIII direct nitration of 6-chloro-4-hydroxy-5- methylpyridin-2(lH)-one hydrochloride hydrate is carried out in excess sulfuric acid and one equivalent of nitric acid to provide 6-chloro-4-hydroxy-5-methyl-3-nitropyridin- 2(lH)-one.
• the reaction is run at a reduced temperature.
• the product conveniently can be precipitated from the solution by the addition of ice water.
• step (3) of Reaction Scheme XIII 6-chloro-4-hydroxy-5-methyl-3-nitropyridin- 2(lH)-one is converted to the triflate of Formula LXXII.
• the reaction can be carried out by adding trifluoromethanesulfonic anhydride to a solution of 6-chloro-4-hydroxy-5- methyl-3-nitropyridin-2(lH)-one in a suitable solvent such as dichloromethane in the presence of a base such as triethylamine.
• the reaction can be carried out at sub-ambient temperatures.
• An amine of Formula XXIV is then added to the reaction at ambient temperature to provide a pyridine of Formula LXXII.
• the product can be isolated from the reaction mixture using conventional methods.
• step (4) of Reaction Scheme XIII the triflate group of a compound of Formula LXXII is displaced with bis(4-methoxybenzyl)amine to provide a pyridine of Formula LXXIII.
• the reaction can be carried out in the presence of a base such as triethylamine and in a suitable solvent such as toluene. The reaction is conveniently carried out at elevated temperatures. The product can be isolated from the reaction mixture using conventional methods.
• step (5) of Reaction Scheme XIII the nitre group of a compound of Formula
• LXXIII is reduced to provide a ⁇ yridine-7,8-diamine of Formula LXXIV.
• the reaction can be carried out by the addition of sodium borohydride and nickel chloride to a solution of a compound of Formula LXXIII in a suitable solvent or solvent mixture such as methanol/dichloromethane at ambient temperature.
• the product can be isolated from the reaction mixture using conventional methods.
• step (6) of Reaction Scheme XIII a pyridine-7,8-diamine of Formula LXXIV reacts with a carboxylic acid or an equivalent thereof to provide an imidazo[4,5-c]pyridine of Formula LXXV.
• the reaction can be carried out as described in step (4) of Reaction Scheme VIII.
• step (7) of Reaction Scheme XIII an imidazo[4,5-c]pyridine of Formula LXXV is deprotected under acidic conditions to provide a lH-imidazo[4,5-c]pyridin-4-amine of Formula LXXVI.
• the reaction can be carried out by dissolving an imidazo[4,5-c]pyridine of Formula LXXV in trifluoroacetic acid and stirring at ambient temperature.
• the reaction can be carried out in a suitable solvent such as dichloromethane.
• step (8) of Reaction Scheme XIII a lH-imidazo[4,5-c]pyridin-4-amine of Formula LXXVI is converted to a l ⁇ -imidazo[4,5-c]pyridin-4-amine of Formula LXXVII-1, 2,3, which is a subgenus of Formula I-l, 1-2, and 1-2, using conventional methods.
• the reaction can be carried out as described in step (11) of Reaction Scheme II.
• reduction of the nitro group at the 3 -position of the pyridine ring can be carried out by using the Ni 2 B reduction without reducing the alkenyl, alkynyl, alkenylene, or alkynylene group.
• a readily reducible group such as an alkenyl or heteroaryl group
• the formation of an N-triphenylphosphinyl compound followed by hydrolysis can be used in place of the reductive removal to preserve , for example, the alkenyl or heteroaryl group.
• non-interfering substituents refers to Rx, R ⁇ 5 and Rz groups which do not prevent a compound of Formula la from inducing the biosynthesis of one or more cytokines.
• Illustrative non-interfering Rx groups include those described above for R 2 .
• Illustrative non-interfering R Y and Rz groups include those described above for R 3 and j.
• alkyl alkenyl
• alkynyl alkynyl
• prefix “alk-” are inclusive of both straight chain and branched chain groups and of cyclic groups, i.e. cycloalkyl and cycloalkenyl.
• these groups contain from 1 to 20 carbon atoms, with alkenyl groups containing from 2 to 20 carbon atoms, and alkynyl groups containing from 2 to 20 carbon atoms.
• Preferred groups have a total of up to 10 carbon atoms, for example, up to 8 carbon atoms, up to 6 carbon atoms, and up to 4 carbon atoms.
• Cyclic groups can be monocyclic or polycyclic and preferably have from 3 to 10 ring carbon atoms.
• Exemplary cyclic groups include cyclopropyl, cyclopropylmethyl, cyclopentyl, cyclohexyl, adamantyl, and substituted and unsubstituted norbomyl and norbornenyl.
• alkylene alkenylene
• alkynylene are the divalent forms of "alkyl”, “alkenyl”, and “alkynyl” defined above.
• haloalkyl is inclusive of groups that are substituted by one or more halogen atoms, including perfluorinated groups. This is also true of groups that include the prefix
• halo- examples of suitable haloalkyl groups are chloromethyl, trifluoromethyl, and the like.
• aryl as used herein includes carbocyclic aromatic rings or ring systems. Examples of aryl groups include phenyl, naphthyl, biphenyl, fluorenyl and indenyl.
• heteroaryl includes aromatic rings or ring systems that contain at least one ring heteroatom (e.g., O, S, ⁇ ).
• Suitable heteroaryl groups include furyl, thienyl, pyridyl, quinolinyl, isoquinolinyl, indolyl, isoindolyl, triazolyl, pyrrolyl, tetrazolyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, benzofuranyl, benzothiophenyl, carbazolyl, benzoxazolyl, pyrimidinyl, benzimidazolyl, quinoxalinyl, benzothiazolyl, naphthyridinyl, isoxazolyl, isothiazolyl, purinyl, quinazolinyl, and so on.
• Heterocyclyl includes non-aromatic rings or ring systems that contain at least one ring heteroatom (e.g., O, S, N) and includes all of the fully saturated and partially unsaturated derivatives of the above mentioned heteroaryl groups.
• exemplary heterocyclic groups include pyrrolidinyl, tetrahydrofuranyl, morpholinyl, thiomorpholinyl, piperidinyl, piperazinyl, thiazolidinyl, imidazolidinyl, isothiazolidinyl, and the like.
• the aryl, heteroaryl, and heterocyclyl groups can be unsubstituted or substituted by one or more substituents independently selected from the group consisting of alkyl, alkoxy, methylenedioxy, ethylenedioxy, alkylthio, haloalkyl, haloalkoxy, haloalkylthio, halogen, nitro, hydroxy, mercapto, cyano, carboxy, formyl, aryl, aryloxy, arylthio, arylalkoxy, arylalkylthio, heteroaryl, heteroaryloxy, heteroarylthio, heteroarylalkoxy, heteroarylalkylthio, amino, alkylamino, dialkylamino, heterocyclyl, heterocycloalkyl, alkylcarbonyl, alkenylcarbonyl, alkoxycarbonyl, haloalkylcarbonyl, haloalkoxycarbonyl, alkylthiocarbonyl
• any other groups are identified as being “substituted” or “optionally substituted”, then those groups can also be substituted by one or more of the above enumerated substituents.
• the invention is inclusive of the compounds described herein in any of their pharmaceutically acceptable forms, including isomers (e.g., diastereomers and enantiomers), salts, solvates, polymorphs, and the like.
• the invention specifically includes each of the compound's enantiomers as well as racemic mixtures of the enantiomers.
• Preferred compounds of the invention include:

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