WO2002046189A2 - Aryl ether substituted imidazoquinolines - Google Patents
Aryl ether substituted imidazoquinolines Download PDFInfo
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- WO2002046189A2 WO2002046189A2 PCT/US2001/046581 US0146581W WO0246189A2 WO 2002046189 A2 WO2002046189 A2 WO 2002046189A2 US 0146581 W US0146581 W US 0146581W WO 0246189 A2 WO0246189 A2 WO 0246189A2
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- Prior art keywords
- alkyl
- imidazo
- aryl
- alkenyl
- quinolin
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- PKWYDYNYHFGUID-UHFFFAOYSA-N CN(C)c1cc(CCCOCC[n]2c(c(cccc3)c3nc3N)c3nc2)ccc1 Chemical compound CN(C)c1cc(CCCOCC[n]2c(c(cccc3)c3nc3N)c3nc2)ccc1 PKWYDYNYHFGUID-UHFFFAOYSA-N 0.000 description 1
- JEJUNJMVZLMGRX-UHFFFAOYSA-N CN(C)c1ccc(CCCOCC[n]2c3c(cccc4)c4nc(N)c3nc2)cc1 Chemical compound CN(C)c1ccc(CCCOCC[n]2c3c(cccc4)c4nc(N)c3nc2)cc1 JEJUNJMVZLMGRX-UHFFFAOYSA-N 0.000 description 1
- 0 CO*[n]1c(C([C@](C=C*)N=C2N)C=CCN)c2nc1* Chemical compound CO*[n]1c(C([C@](C=C*)N=C2N)C=CCN)c2nc1* 0.000 description 1
- UJHWTLJEEZMABH-UHFFFAOYSA-N Cc1nc2c(N)nc(cccc3)c3c2[n]1CCOCCCc1ccccc1 Chemical compound Cc1nc2c(N)nc(cccc3)c3c2[n]1CCOCCCc1ccccc1 UJHWTLJEEZMABH-UHFFFAOYSA-N 0.000 description 1
- CEPZKBSZAZTUPK-UHFFFAOYSA-N Nc1c2nc(C3COCC3)[n](CCOc3ccccc3)c2c(cccc2)c2n1 Chemical compound Nc1c2nc(C3COCC3)[n](CCOc3ccccc3)c2c(cccc2)c2n1 CEPZKBSZAZTUPK-UHFFFAOYSA-N 0.000 description 1
- WVWKUNHGONTMSJ-UHFFFAOYSA-N Nc1c2nc[n](CCOCCCc3ccccc3)c2c(cccc2)c2n1 Chemical compound Nc1c2nc[n](CCOCCCc3ccccc3)c2c(cccc2)c2n1 WVWKUNHGONTMSJ-UHFFFAOYSA-N 0.000 description 1
- CZJBOKJIPCNOSB-UHFFFAOYSA-N Nc1c2nc[n](COCc3ccccc3)c2c(cccc2)c2n1 Chemical compound Nc1c2nc[n](COCc3ccccc3)c2c(cccc2)c2n1 CZJBOKJIPCNOSB-UHFFFAOYSA-N 0.000 description 1
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- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4745—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
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Definitions
- This invention relates to imidazoquinoline compounds that have a 1 -substituent that contains ether and aryl or alkenyl functionality, and to pharmaceutical compositions containing such compounds.
- a further aspect of this invention relates to the use of these compounds as immunomodulators, for inducing cytokine biosynthesis in animals, and in the treatment of diseases, including viral and neoplastic diseases.
- this invention provides imidazo[4, 5-c]quinoline-4- amine and tetrahydroimidazo[4, 5-c]quinoline-4-amine compounds that have an ether containing substituent at the 1 -position.
- the compounds are described by Formulas (I), (II), (III) and (IV), which are defined in more detail infra. These compounds share the general structural formula:
- X, R l9 R 2 , and R are as defined herein for each class of compounds having Formulas (I), (II), (III) and (IV).
- the compounds of Formulas (I), (II), (III), and (IV) are useful as immune response modifiers due to their ability to induce cytokine biosynthesis and otherwise modulate the immune response when administered to animals. This makes the compounds useful in the treatment of a variety of conditions such as viral diseases and tumors that are responsive to such changes in the immune response.
- the invention further provides pharmaceutical compositions containing the immune response modifying compounds, and methods of inducing cytokine biosynthesis in an animal, treating a viral infection in an animal, and/or treating a neoplastic disease in an animal by administering a compound of Formula (I), (II), (III), or (IV) to the animal.
- the invention provides methods of synthesizing the compounds of the invention and intermediates useful in the synthesis of these compounds.
- Imidazoquinoline compounds of the invention which have ether and aryl or alkenyl functionality at the 1 -position are represented by Formula (I):
- X is -CHR 3 -, -CHR 3 -alkyl-, or-CHR 3 -alkenyl-;
- Ri is selected from the group consisting of:
- R 2 is selected from the group consisting of:
- R4 is alkyl or alkenyl, both of which may be interrupted by one or more -O- groups; each R 3 is independently H or C ⁇ - 10 alkyl; each Y is independently -O- or -S(O) 0 - 2 -; n is 0 to 4; and each R present is independently selected from the group consisting of C-- 10 alkyl, C ⁇ - 1 0 alkoxy, hydroxy, halogen and trifluoromethyl; or a pharmaceutically acceptable salt thereof.
- the invention also provides imidazoquinoline compounds that contain ether functionality at the 1 -position, where the ether containing substituent also contains an alkynyl group.
- These compounds are represented by structural formula (II):
- X is -CHR 3 -, -CHR 3 -alkyl-, or -CHR 3 -alkenyl-; Rio is selected from the group consisting of: -H; -alkyl;
- R 2 is selected from the group consisting of: -hydrogen; -alkyl; -alkenyl; -aryl;
- the invention also includes tetrahydroimidazoquinoline compounds that bear an ether and aryl or alkenyl containing substituent at the 1 -position.
- tetrahydroimidazoquinoline compounds are represented by Formula (III):
- X is -CHR 3 -, -CHR 3 -alkyl-, or -CHR 3 -alkenyl-;
- Ri is selected from the group consisting of: aryl; alkenyl; and R 4 -aryl;
- R 2 is selected from the group consisting of:
- R 4 is alkyl or alkenyl, both of which may be interrupted by one or more -O- groups; each R 3 is independently H or Ci-io alkyl; each Y is independently -O- or -S(0)o- 2 -; n is 0 to 4; and each R present is independently selected from the group consisting of Ci-io alkyl, Ci-io alkoxy, hydroxy, halogen and trifluoromethyl; or a pharmaceutically acceptable salt thereof.
- An additional class of immune response modifying compounds of the invention are tetrahydroimidazoquinoline compounds that have an ether containing substituent at the 1- position, where the ether containing substituent also contains an alkynyl group. These compounds are represented by structural formula (IV):
- X is -CHR 3 -, -CHR 3 -alkyl-, or-CHR 3 -alkenyl-; Rio is selected from the group consisting of: -H; -alkyl;
- R 2 is selected from the group consisting of: -hydrogen; -alkyl; -alkenyl; -aryl;
- each R 3 is independently H or C MO alkyl; each Y is independently -O- or - S(0)o- 2 -; n is ⁇ to 4; and each R present is independently selected from the group consisting of C MO alkyl, C O alkoxy, hydroxy, halogen and trifluoromethyl; or a pharmaceutically acceptable salt thereof.
- a 4-amino-lH-imidazo[4,5-c]quinolin- 1-yl alcohol of Formula X is alkylated with a halide of Formula XI to provide a lH-imidazo[4,5- c]quinolin-4-amine of Formula XII which is a subgenus of Formula I.
- the alcohol of Formula X is reacted with sodium hydride in a suitable solvent such as N,N- dimethylformamide to form an alkoxide.
- the halide is then added to the reaction mixture.
- the reaction can be carried out at ambient temperature or with gentle heating ( ⁇ 50°C) if desired.
- the product or a pharmaceutically acceptable salt thereof can be isolated using conventional methods.
- step (1) of Reaction Scheme II a lH-imidazo[4,5-c]quinolin-l-yl alcohol of Formula XIII is alkylated with a halide of Formula XI to provide a lH-imidazo[4,5- c]quinolin- 1 -yl ether of Formula XIV.
- the alcohol of Formula XIII is reacted with sodium hydride in a suitable solvent such as N,N-dimethylformamide or tetrahydrofuran to form an alkoxide.
- the alcohol and the halide can be combined in a biphasic mixture of aqueous 50% sodium hydroxide and an inert solvent such as dichloromethane in the presence of a phase transfer catalyst such as benzyltrimethylammonium chloride.
- the reaction can be carried out at ambient temperature.
- Many compounds of Formula XIII are known, see for example, Gerster, U.S. Patent 4,689,338; others can readily be prepared using known synthetic routes, see for example, Gerster et al., U.S. Patent No. 5,605,899 and Gerster, U.S. Patent No. 5,175,296.
- step (2) of Reaction Scheme II a lH-imidazo[4,5-c]quinolin-l-yl ether of
- Formula XIV is oxidized to provide a lH-imidazo[4,5-c]quinoline-5N-oxide of Formula XV using a conventional oxidizing agent capable of forming N-oxides.
- a solution of a compound of Formula XIV in a suitable solvent such as chloroform or dichloromethane is oxidized using 3-chloroperoxybenzoic acid at ambient temperature.
- Step (3) involves (i) reacting a compound of Formula XV with an acylating agent and then (ii) reacting the product with an animating agent. Part (i) of step (3) involves reacting an N-oxide of Formula XV with an acylating agent.
- Suitable acylating agents include alkyl- or arylsulfonyl chlorides (e.g., benezenesulfonyl chloride, methanesulfonyl chloride, p-toluenesulfonyl chloride).
- Part (ii) of step (3) involves reacting the product of part (i) with an excess of an aminating agent.
- Suitable aminating agents include ammonia (e.g., in the form of ammonium hydroxide) and ammonium salts (e.g., ammonium carbonate, ammonium bicarbonate, ammonium phosphate).
- Ammonium hydroxide is preferred.
- the reaction is preferably carried out by dissolving the N-oxide of Formula XV in an inert solvent such as dichloromethane, adding the aminating agent to the solution, and then slowly adding the acylating agent.
- the product or a pharmaceutically acceptable salt thereof can be isolated using conventional methods.
- step (3) may be carried out by (i) reacting an N-oxide of Formula XV with an isocyanate and then (ii) hydrolyzing the resulting product.
- Part (i) involves reacting the N-oxide with an isocyanate wherein the isocyanato group is bonded to a carbonyl group.
- Preferred isocyanates include trichloroacetyl isocyanate and aroyl isocyanates such as benzoyl isocyanate.
- the reaction of the isocyanate with the N-oxide is carried out under substantially anhydrous conditions by adding the isocyanate to a solution of the N-oxide in an inert solvent such as chloroform or dichloromethane.
- Part (ii) involves hydrolysis of the product from part (i).
- the hydrolysis can be carried out by conventional methods such as heating in the presence of water or a lower alkanol optionally in the presence of a catalyst such as an alkali metal hydroxide or lower alkoxide.
- a catalyst such as an alkali metal hydroxide or lower alkoxide.
- the product or a pharmaceutically acceptable salt thereof can be isolated using conventional methods.
- Reaction Scheme III a 4-amino-lH-imidazo[4,5-c]quinolin-l-yl alcohol of Formula X is condensed with a phenol of Formula XVI to provide a lH-imidazo[4,5- c]quinolin-4-amine of Formula XVII which is a subgenus of Formula I.
- a solution of a compound of Formula X and the phenol in a suitable solvent such as N,N- dimethylformamide is treated with diethyl azodicarboxylate and triphenylphosphine at ambient temperature.
- the product or a pharmaceutically acceptable salt thereof can be isolated using conventional methods.
- step (1) of Reaction Scheme IV the hydroxy group of a lH-imidazo[4,5- c]quinolin-l-yl alcohol of Formula XIII is protected with a benzyl group.
- the alcohol of Formula XIII is reacted with sodium hydride in a suitable solvent such as N,N- dimethylformamide to form an alkoxide.
- the alkoxide is then alkylated with benzyl bromide to provide a compound of Formula XVIII.
- the reaction can be carried out at ambient temperature.
- step (2) of Reaction Scheme IV a compound of Formula XVIII is oxidized using the method of step (2) of Reaction Scheme II to provide a lH-imidazo[4,5-c]quinoline- 5N-oxide of Formula XIX.
- step (3) of Reaction Scheme IV a lH-imidazo[4,5-c]quinoline-5N-oxide of Formula XIX is chlorinated to provide a 4-chloro-lH-imidazo[4,5-c]quinoline of Formula XX.
- a solution of a compound of Formula XIX in a suitable solvent such as toluene is treated with phosphorous oxychloride at ambient temperature.
- step (4) of Reaction Scheme IV a 4-chloro-lH-imidazo[4,5-c]quinoline of Formula XX is reacted with phenol to provide a 4-phenoxy-lH-imidazo[4,5-c]quinoline of Formula XXI.
- the phenol is reacted with sodium hydride in a suitable solvent such as diglyme to form a phenoxide.
- the phenoxide is then reacted at an elevated temperature with a compound of Formula XX.
- step (5) of Reaction Scheme IV the benzyl protecting group is removed from a compound of Formula XXI to provide a 4-phenoxy-lH-imidazo[4,5-c]quinolin-l-yl alcohol of Formula XXII.
- the reaction is preferably carried out by adding triflic acid in a controlled fashion to a solution of a compound of Formula XXI in a suitable solvent such as dichloromethane at ambient temperature.
- step (6) of Reaction Scheme IV a 4-phenoxy-lH-imidazo[4,5-c]quinolin-l-yl alcohol of Formula XXII is alkylated with a halide of ⁇ al-Rn to provide a 4-phenoxy-lH- imidazo[4,5-c]quinolin-l-yl ether of Formula XXIII.
- Formula XXII is formed by adding the alcohol to a biphasic mixture of aqueous 50% sodium hydroxide and an inert solvent such as dichloromethane in the presence of a phase transfer catalyst such as benzyltrimethlammonium chloride. The alkoxide is then alkylated. The reaction can be carried out at ambient temperature.
- a 4-phenoxy-lH-imidazo[4,5-c]quinolin-l-yI ether of Formula XXIII is aminated to provide a lH-imidazo[4,5-c]quinolin-4-amine of Formula XII which is a subgenus of Formula I.
- the reaction can be carried out by combining a compound of Formula XXIII with ammonium acetate and heating the resulting mixture at ⁇ 150°C.
- the product or a pharmaceutically acceptable salt thereof can be isolated using conventional methods.
- Tetrahydroimidazoquinolines of the invention can be prepared according to Reaction Scheme V where R, R 2 , Rn, X and n are as defined above.
- a 4-amino-6,7,8,9-tetrahydro-lH-imidazo[4,5-c]quinolin-l- yl alcohol of Formula XXIV is alkylated with a halide of Formula XI to provide a 6,7,8,9- tetrahydro-lH-imidazo[4,5-c]quinolin-4-amine of Formula XXV which is a subgenus of Formula III.
- the alcohol of Formula XXIV is reacted with sodium hydride in a suitable solvent such as N,N-dimethylformamide to form an alkoxide.
- the alkoxide is then combined with the halide.
- the reaction can be carried out at ambient temperature.
- the product or a pharmaceutically acceptable salt thereof can be isolated using conventional methods.
- step (1) of Reaction Scheme VI a 4-chloro-3-nitroquinoline of Formula XXVI is reacted with an amine of Formula R ⁇ -0-X-NH 2 to provide a 3-nitroquinolin-4-amine of Formula XXVII.
- the reaction can be carried out by adding the amine to a solution of a compound of Formula XXVI in a suitable solvent such as chloroform or dichloromethane and optionally heating.
- a suitable solvent such as chloroform or dichloromethane
- step (2) of Reaction Scheme VI a 3-nitroquinolin-4-amine of Formula XXVII is reduced to provide a quinoline-3,4-diamine of Formula XXVIII.
- the reduction is carried out using a conventional heterogeneous hydrogenation catalyst such as platinum on carbon or palladium on carbon.
- the reaction can conveniently be carried out on a Parr apparatus in a suitable solvent such as isopropyl alcohol or preferably toluene.
- step (3) of Reaction Scheme VI a quinoline-3,4-diamine of Formula XXVIII is reacted with a carboxylic acid or an equivalent thereof to provide a lH-imidazo[4,5- c]quinoline of Formula XXIX.
- Suitable equivalents to 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 XXIX.
- triethyl orthoformate will provide a compound where R 2 is hydrogen and triethyl orthoacetate will provide a compound where R 2 is methyl.
- 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 XXVIII with an acyl halide of Formula R 2 C(0)C1 and then (ii) cyclizing.
- the acyl halide is added to a solution of the diamine in a suitable solvent such as acetonitrile, pyridine or dichloromethane.
- the reaction can be carried out at ambient temperature.
- the product of part (i) is heated in an alcoholic solvent in the presence of a base.
- step (i) is refluxed in ethanol in the presence of an excess of triethylamine or heated with methanolic ammonia.
- step (ii) can be carried out by heating the reaction mixture after analysis indicates that step (i) is complete.
- step (4) of Reaction Scheme VI a lH-imidazo[4,5-c]quinoline of Formula XXIX is oxidized using the method of step (2) of Reaction Scheme II to provide a 1H- imidazo[4,5-c]quinoline-5N-oxide of Formula XXX
- step (5) of Reaction Scheme VI a lH-imidazo[4,5-c]quinoline-5N-oxide of Formula XXX is aminated using the method of step (3) of Reaction Scheme II to provide a lH-imidazo[4,5-c]quinolin-4-amine of Formula I.
- step (1) of Reaction Scheme VII a lH-imidazo[4,5-c]quinolin-l-yl alcohol of
- Formula XIII is alkylated with a halide of Formula XXXI to provide a lH-imidazo[4,5- c]quinolin-l-yl ether of Formula XXXII.
- the compound of Formula XIII and the halide of Formula XXXI are combined in a biphasic mixture of 50% aqueous sodium hydroxide and a suitable solvent such as dichloromethane in the presence of a phase transfer catalyst such as benzyltrimethylammonium chloride.
- the reaction can be run at ambient temperature.
- step (2) of Reaction Scheme VII a lH-imidazo[4,5-c]quinoline of Formula
- XXXII is oxidized using the method of step (2) of Reaction Scheme II to provide a 1H- imidazo[4,5-c]quinoline-5N-oxide of Formula XXXIII.
- step (3) of Reaction Scheme VII a lH-imidazo[4,5-c]quinoline-5N-oxide of
- Formula XXXIII is reacted with trichloroacetyl isocyanate to provide a lH-imidazo[4,5- e]quinolin-4-yl trichloroacetamide of Formula XXXIV.
- the isocyanate is added in a controlled fashion at ambient temperature to a solution of the 5N-oxide in a suitable solvent such as dichloromethane.
- step (4) of Reaction Scheme VII a lH-imidazo[4,5-c]quinolin-4-yl trichloroacetamide of Formula XXXIV is hydrolyzed to provide a lH-imidazo[4,5- c]quinolin-4-amine of Formula XXXV which is a subgenus of Formula II.
- the hydrolysis can be carried out by conventional methods, preferably by treating a solution of a compound of Formula XXXIV in methanol with sodium methoxide.
- step (5) of Reaction Scheme VII lH-imidazo[4,5-c]quinolin-4-amine of Formula XXXV is coupled with a halide of formula ⁇ al-R ⁇ 2 using a transition metal catalyst to provide a lH-imidazo[4,5-c]quinolin-4-amine of Formula XXXVT which is a subgenus of Formula II.
- a compound of Formula XXXV is combined with the halide in the presence of copper (I) iodide, dichlorobis(triphenylphosphine)paIladium(II), and excess triethylamine in a suitable solvent such as N,N-dimethylformamide or acetonitrile.
- the reaction is preferably carried out at an elevated temperature (60-80°C).
- the product or a pharmaceutically acceptable salt thereof can be isolated using conventional methods.
- Step (1) of Reaction Scheme VIII the amino group of a lH-imidazo[4,5- c]quinolin-4-amine of Formula XXXV is protected with two tert-butoxycarbonyl groups.
- a compound of Formula XXXV is combined with di-tert-butyl dicarbonate in a suitable solvent such as N,N-dimethylformamide in the presence of 4-(dimethylamino)pyridine and triethylamine. The reaction is carried out at an elevated temperature (80-85°C).
- a protected lH-imidazo[4,5-c]quinolin-4- amine of Formula XXXVII is coupled with a halide of formula ⁇ al-R ⁇ 2 using a transition metal catalyst to provide a protected lH-imidazo[4,5-c]quinolin-4-amine of Formula XXXVIII.
- a compound of Formula XXXVII is combined with the halide in the presence of copper (I) iodide, dichlorobis(triphenylphosphine)palladium(II), and excess triethylamine in a suitable solvent such as N,N-dimethylformamide or acetonitrile.
- the reaction can be carried out at ambient temperature or at an elevated temperature (40-80°C).
- step (3) of Reaction Scheme VIII the protecting groups are removed by hydrolysis under acidic conditions to provide a lH-imidazo[4,5-c]quinolin-4-amine of Formula XXXVI which is a subgenus of Formula II.
- a compound of Formula XXXVIII is treated with trifluoroacetic acid in a suitable solvent such as dichloromethane.
- the reaction can be run at ambient temperature or at a reduced temperature (0°C).
- the product or a pharmaceutically acceptable salt thereof can be isolated using conventional methods.
- step (4) of Reaction Scheme VIII the alkyne bond of a protected ⁇ H- imidazo[4,5-c]quinolin-4-amine of Formula XXXVIII is reduced to provide a protected lH-imidazo[4,5-c]quinolin-4-amine of Formula XXXIX.
- the reduction is carried out using a conventional heterogeneous hydrogentation 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.
- step (5) of Reaction Scheme VIII the protecting groups of a compound of Formula XXXIX are removed in the same manner as in step (3) to provide a 1H- imidazo[4,5-c]quinolin-4-amine of Formula XL which is a subgenus of Formula I.
- the product or a pharmaceutically acceptable salt thereof can be isolated using conventional methods.
- step (1) of Reaction Scheme IX the amino group of a lH-imidazo[4,5- c]quinolin-4-amine of Formula XXXV is protected with benzyloxycarbonyl groups.
- a compound of Formula XXXV is combined with dibenzyl dicarbonate in a suitable solvent such as N,N-dimethylformamide. The reaction can be carried out at ambient temperature or with mild heating (40°C).
- a protected lH-imidazo[4,5-c]quinolin-4-amine of Formula XLI is coupled with a halide of formula ⁇ al-Rj 2 using a transition metal catalyst to provide a protected lH-imidazo[4,5-c]quinolin-4-amine of Formula XLII.
- a compound of Formula XLI is combined with the halide in the presence of copper (I) iodide, dichlorobis(triphenylphosphine)palladium(II), and excess triethylamine in a suitable solvent such as N,N-dimethylformamide or acetonitrile.
- the reaction can be carried out at ambient temperature or at an elevated temperature (40-80°C).
- step (3) of Reaction Scheme IX the protecting groups are removed by hydrolysis to provide a lH-imidazo[4,5-c]quinolin-4-amine of Formula XXXVI which is a subgenus of Formula II.
- a compound of Formula XLII is treated with sodium methoxide in a suitable solvent such as methanol.
- the reaction can be run at ambient temperature.
- the product or a pharmaceutically acceptable salt thereof can be isolated using conventional methods.
- step (4) of Reaction Scheme IX the protecting groups of a compound of Formula XLII are removed by hydrogenolysis and the alkyne bond is reduced to provide a lH-imidazo[4,5-c]quinolin-4-amine of Formula XL which is a subgenus of Formula I.
- the hydrogenolysis/reduction is carried out using palladium hydroxide on carbon.
- the reaction can conveniently be carried out on a Parr apparatus in a suitable solvent such as methanol.
- the product or a pharmaceutically acceptable salt thereof can be isolated using conventional methods.
- step (1) of Reaction Scheme X a 2,4-dichloro-3-nitroquinoline of Formula XLIII is reacted with an amine of Formula R ⁇ -0-X-NH 2 to provide a 2-chloro-3-nitroquinolin-4- amine of Formula XLIV.
- the reaction can be carried out by adding the amine to a solution of a compound of Formula XLIII in a suitable solvent such as chloroform or dichloromethane and optionally heating.
- a suitable solvent such as chloroform or dichloromethane
- step (2) of Reaction Scheme X a 2-chloro-3-nitroquinolin-4-amine of Formula XLIV is reduced using the method of step (2) in Reaction Scheme VI to provide a 2- chloroquinoline-3,4-diamine of Formula XLV.
- step (3) of Reaction Scheme X a 2-chloroquinoline-3,4-diamine of Formula XLV is cyclized using the method of step (3) in Reaction Scheme VI to provide a 4- chloro-lH-imidazo[4,5-c]quinoline of Formula XL VI.
- step (4) of Reaction Scheme X a 4-chloro-lH-imidazo[4,5-c]quinoline of Formula XL VI is aminated to provide a lH-imidazo[4,5-c]quinolin-4-amine of Formula I.
- the reaction is carried out by heating (e.g.,125-175°C) a compound of Formula XL VI under pressure in a sealed reactor in the presence of a solution of ammonia in an alkanol.
- the product or a pharmaceutically acceptable salt thereof can be isolated using conventional methods.
- Reaction Scheme XI where- R, R], R 2 , X and n are as defined above.
- a lH-imidazo[4,5-c]quinolin-4-amine of Formula XLVII is alkylated with a halide of Formula XLVIII to provide a lH-imidazo[4,5-c]quinolin-4- amine of Formula I.
- the compound of Formula XLVII is reacted with sodium hydride in a suitable solvent such as N,N-dimethylformamide.
- the halide is then added to the reaction mixture.
- the reaction can be carried out at an elevated temperature ( ⁇ 100°C). Alkylation occurs at both the Nl and the N3 nitrogens; however, the desired 1-isomer can be readily separated from the 3-isomer using conventional techniques such as column chromatography and recrystallization.
- step (1) of Reaction Scheme XII a 4-nitrotetrazolo[l,5-a]quinolin-5-ol of Formula XLIX is chlorinated to provide a 5-chloro-4-nitrotetrazolo[l,5-a]quinoIine of
- step (2) of Reaction Scheme XII a 5-chloro-4-nitrotetrazolo[l,5-a]quinoline of Formula L is reacted with an amine of Formula R ⁇ -0-X-N ⁇ 2 to provide a 4- nitrotetrazolo[l,5-a]quinolin-5-amine of Formula LI.
- the reaction can be carried out by adding the amine to a solution of a compound of Formula L in a suitable solvent such as dichloromethane in the presence of triethylamine.
- step (3) of Reaction Scheme XII a 4-nitrotetrazolo[l,5-a]quinolin-5-amine of Formula LI is reduced using the method of step (2) in Reaction Scheme VI to provide a tetrazolo[l,5-a]quinolin-4,5-diamine of Formula LII.
- step (4 ) of Reaction Scheme XII a tetrazolo[l,5-a]quinolin-4,5-diamine of Formula LII is cyclized using the method of step (3) in Reaction Scheme VI to provide a 6H-imidazo[4,5-c]tetrazolo[l,5- ]quinoline of Formula LIII.
- step (5) of Reaction Scheme XII a 6H-imidazo[4,5-c]tetrazolo[l,5- ⁇ ]quinoline of Formula LIII is reduced to provide a lH-imidazo[4,5-c]quinolin- 4-amine of Formula I.
- Step (5) involves (i) reacting a compound of Formula LIII with triphenylphosphine and then (ii) hydrolyzing.
- Part (i) can be carried out by combining a compound of Formula LIII with triphenylphosphine in a suitable solvent such as 1,2-dichlorobenzene and heating.
- Part (ii) involves hydrolysis of the product from part (i). The hydrolysis can be carried out by conventional methods such as heating in the presence of water or a lower alkanol optionally in the presence of a catalyst such as an alkali metal hydroxide or lower alkoxide.
- the product or a pharmaceutically acceptable salt thereof can be isolated using conventional methods.
- Formula XXXII is coupled with a halide of Formula ⁇ al-Rj 2 using the method of step (5) in Reaction Scheme VII to provide a lH-imidazo[4,5-c]quinolin-l-yl ether of Formula LIV.
- step (2) of Reaction Scheme XIII a lH-imidazo[4,5-c]quinolin-l-yl ether of Formula LIV is oxidized using the method of step (2) in Reaction Scheme II to provide a lH-imidazo[4,5-c]quinoline-5N-oxide of Formula LV.
- step (3) of Reaction Scheme XIII a lH-imidazo[4,5-c]quinoline-5N-oxide of Formula LV is aminated using the method of step (3) in Reaction Scheme II to provide a lH-imidazo[4,5-c]quinolin-4-amine of Formula XXXVI which is a subgenus of Formula II.
- the product or a pharmaceutically acceptable salt thereof can be isolated using conventional methods.
- step (1) of Reaction Scheme XIV the alkyne bond of a lH-imidazo[4,5- c]quinolin-l-yl ether of Fonnula LIV is reduced using the method of step (4) of Reaction Scheme VIII to provide a lH-imidazo[4,5-c]quinolin-l-yl ether of Formula LVI.
- step (2) of Reaction Scheme XIV a lH-imidazo[4,5-c]quinolin-l-yl ether of Formula LVI is oxidized using the method of step (2) in Reaction Scheme II to provide a lH-imidazo[4,5-c]quinoline-5 ⁇ -oxide of Formula LVII.
- step (3) of Reaction Scheme XIV a lH-imidazo[4,5-c]quinoline-5N-oxide of Formula LVII is aminated using the method of step (3) in Reaction Scheme II to provide a lH-imidazo[4,5-c]quinolin-4-amine of Formula XL which is a subgenus of Formula I.
- the product or a pharmaceutically acceptable salt thereof can be isolated using conventional methods.
- Tetrahydroimidazoquinolines of the invention can be prepared according to Reaction Scheme XV where R, R 2 , R 12 , X and n are as defined above.
- step (1) of Reaction Scheme XV a 4-amino-6,7,8,9-tetrahydro-lH-imidazo[4,5- c]quinolin-l-yl alcohol of Formula XXIV is alkylated using the method described in Reaction Scheme V with a halide of Formula ⁇ al-(C ⁇ 2 ) ⁇ - ⁇ 0 -C ⁇ C ⁇ to provide a 6,7,8,9- tetrahydro-lH-imidazo[4,5-c]quinolin-4-amine of Formula LVIII which is a subgenus of Formula IV.
- step (2) of Reaction Scheme XV a 6,7,8,9-tetrahydro-lH-imidazo[4,5- c]quinolin-4-amine of Formula LVIII is coupled using the method of step (5) of Reaction Scheme VII with a halide of Formula ⁇ al-R ⁇ 2 to provide a 6,7,8,9-tetrahydro-lH- imidazo[4,5-c]quinolin-4-amine of Formula LIX which is a subgenus of Formula IV.
- the product or a pharmaceutically acceptable salt thereof can be isolated using conventional methods.
- Step (1) of Reaction Scheme XVI a 2,4-dihydroxy-3-nitro-6,7,8,9- tetrayhydroquinoline of Formula LX is chlorinated to provide a 2,4-dichloro-3-nitro- 6,7,8,9-tetrayhydroquinoline of Formula LXI.
- Conventional chlorinating agents can be used.
- the reaction is carried out by combining a compound of Formula LX with phosphorous oxychloride and then heating (55-65°C).
- Compounds of Formula LX are known or can be prepared using known synthetic methods (see for example Nikolaides et al,. U.S. Patent 5,352,784 and references cited therein).
- step (2) of Reaction Scheme XVI a 2,4-dichloro-3-nitro-6,7,8,9- tetrayhydroquinoline of Formula LXI is reacted with an amine of Formula R ⁇ -0-X-NH 2 to provide a 2-chloro-3-nitro-6,7,8,9-tetrahydroquinolin-4-amine of Formula LXII.
- the reaction can be carried out by adding the amine to a solution of a compound of Formula
- step (3) of Reaction Scheme XVI a 2-chloro-3-nitro-6,7,8,9-tetrahydroquinolin- 4-amine of Formula LXII is reacted with phenol using the method of step (4) of Reaction Scheme IV to provide a 2-phenoxy-3-nitro-6,7,8,9-tetrahydroquinolin-4-amine of Formula LXIII.
- step (4) of Reaction Scheme XVI a 2-phenoxy-3-nitro-6,7,8,9- tetrahydroquinolin-4-amine of Formula LXIII is reduced using the method of step (2) of Reaction Scheme VI to provide a 2-phenoxy-6,7,8,9-tetrahydroquinolin-3,4-diamine of Formula LXIV.
- step (5) of Reaction Scheme XVI a 2-phenoxy-6,7,8,9-tetrahydroquinolin-3,4- diamine of Formula LXIV is cyclized using the method of step (3) of Reaction Scheme VI to provide a 4-phenoxy-6,7,8,9-tetrahydro-lH-imidazo[4,5-c]quinoline of Formula LXV.
- step (6) of Reaction Scheme XVI a 4-phenoxy-6,7,8,9-tetrahydro-lH- imidazo[4,5-c]quinoline of Formula LXV is aminated using the method of step (7) of Reaction Scheme IV to provide a 6,7,8,9-tetrahydro-lH-imidazo[4,5-c]quinolin-4-amine of Formula III.
- the invention also provides novel compounds useful as intermediates in the synthesis of the compounds of Formulas (I), (II), (III), and (IV). These intermediate compounds have the structural Formulas (V) - (IX), described in more detail below.
- One class of intermediate compounds has formula (V):
- V wherein X is -CHR 3 -, -CHR 3 -alkyl-, or -CHR 3 -alkenyl-; Ri is selected from the group consisting of: -aryl; -alkenyl; -I ⁇ -aryl; and -(CH 2 )M 0 -C ⁇ C-R 10 ; R 2 is selected from the group consisting of: -hydrogen; -alkyl; -alkenyl; -aryl;
- R-t is alkyl or alkenyl, which may be interrupted by one or more -O- groups; each R 3 is independently H or C O alkyl;
- Rio is selected from the group consisting of H, alkyl, alkenyl and aryl; each Y is independently -O- or-S(0)o- 2 S n is 0 to 4; and each R present is independently selected from the group consisting of C MO alkyl, C MO alkoxy, hydroxy, halogen and trifluoromethyl; or a pharmaceutically acceptable salt thereof.
- X is -CHR 3 -, -CHR 3 -alkyI-, or -CHR 3 -aIkenyl-;
- Ri is selected from the group consisting of: -aryl; -alkenyl; -J r-aryl; and -(CH 2 ) O -C ⁇ C-R ⁇ o ;
- R 2 is selected from the group consisting of: -hydrogen; -alkyl; -alkenyl; -aryl; -heteroaryl;
- R 4 is alkyl or alkenyl, both of which may be interrupted by one or more -O- groups; each R3 is independently H or C O alkyl;
- Rio is selected from the group consisting of H, alkyl, alkenyl and aryl; each Y is independently -O- or -S(0)o- 2 -; n is 0 to 4; and each R present is independently selected from the group consisting of CMO alkyl, CM O alkoxy, hydroxy, halogen and trifluoromethyl; or a pharmaceutically acceptable salt thereof.
- intennediate compounds are the imidazoquinoline-N-oxide compounds of formula (VII):
- X is -CHR 3 -, -CHR 3 -alkyl-, or -CHR 3 -alkenyl-;
- Ri is selected from the group consisting of: -aryl; -alkenyl;
- -R-r-aiyl is alkyl or alkenyl, both of which may be interrupted by one or more -O- groups; each R 3 is independently H or C MO alkyl;
- Rio is selected from the group consisting of H, alkyl, alkenyl and aryl; n is 0 to 4; and each R present is independently selected from the group consisting of C MO alkyl, C MO alkoxy, hydroxy, halogen and trifluoromethyl; or a pharmaceutically acceptable salt thereof.
- X is -CHR 3 -, -CHR 3 -alkyl-, or -CHR 3 -alkenyl-;
- Ri is selected from the group consisting of: -aryl; -alkenyl;
- R 2 is selected from the group consisting of: -hydrogen; -alkyl;
- K is alkyl or alkenyl, which may be interrupted by one or more -O- groups; each R 3 is independently H or CM O alkyl;
- R 10 is selected from the group consisting of H, alkyl, alkenyl and aryl; each Y is independently -O- or -S(O) 0 - 2 -; n is 0 to 4; each R present is independently selected from the group consisting of CM O alkyl, CMO alkoxy, hydroxy, halogen and trifluoromethyl; and R 7 is tert-butyl or benzyl; or a pharmaceutically acceptable salt thereof.
- a further class of intermediates are imidazoquinoline-4-chloro compounds of the formula (IX)
- X is -CHR 3 -, -CHR 3 -alkyl-, or -CHR 3 -alkenyl-;
- Ri is selected from the group consisting of: aryl; alkenyl; R-v-aryl; and -(CH 2 )M O -C ⁇ CH R 2 is selected from the group consisting of:
- . is alkyl or alkenyl, which may be interrupted by one or more -O- groups; each R 3 is independently H or CM O alkyl; each Y is independently -O- or -S(0)o- 2 -; n is 0 to 4; and each R present is independently selected from the group consisting of C MO alkyl, CM O alkoxy, hydroxy, halogen and trifluoromethyl; or a pharmaceutically acceptable salt thereof.
- alkyl As used herein, the terms "alkyl”, “alkenyl” and the prefix “alk-” are inclusive of both straight chain and branched chain groups and of cyclic groups, i.e. cycloalkyl and cycloalkenyl. Unless otherwise specified, these groups contain from 1 to 20 carbon atoms, with alkenyl groups containing from 2 to 20 carbon atoms. Preferred groups have a total of up to 10 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, cyclopropylmethyl, and adamantyl.
- alkyl and alkenyl portions of -X- groups can be unsubstituted or substituted by one or more substituents, which substituents are selected from the group consisting of alkyl, alkenyl, aryl, heteroaryl, heterocyclyl, arylalkyl, heteroarylalkyl, and heterocyclylalkyl.
- 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 hetero atom (e.g., O, S, N).
- 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 hetero atom (e.g., O, S, N) and includes all of the fully saturated and partially unsaturated derivatives of any of the above mentioned heteroaryl groups.
- exemplary heterocyclic groups include pyrrolidinyl, tetrahydrofuranyl, morpholinyl, tliiomorpholinyl, 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, 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, arylcarbonyl, heteroarylcarbon
- R- t -aryl is a preferred Rj group and preferred Rio groups are alkyl and aryl, with phenyl or substituted phenyl being a preferred aryl group.
- Preferred R 2 groups include hydrogen, alkyl groups having 1 to 4 carbon atoms (i.e., methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, isobutyl, and cyclopropylmethyl), methoxyethyl, and ethoxymethyl.
- substituted groups such as substituted alkyl or substituted aryl groups
- preferred substituents include halogen, nitrile, nitro, carboxy, methoxy, methylthio, trifluoromethyl, and trifluoromethoxy.
- One or more of these preferred substituents, if present, can be present in the compounds of the invention in any combination.
- 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.
- compositions of the invention contain a therapeutically effective amount of a compound of the invention as described above in combination with a pharmaceutically acceptable carrier.
- a therapeutically effective amount means an amount of the compound sufficient to induce a therapeutic effect, such as cytokine induction, antitumor activity, and/or antiviral activity.
- a therapeutic effect such as cytokine induction, antitumor activity, and/or antiviral activity.
- the exact amount of active compound used in a pharmaceutical composition of the invention will vary according to factors known to those of skill in the art, such as the physical and chemical nature of the compound, the nature of the carrier, and the intended dosing regimen, it is anticipated that the compositions of the invention will contain sufficient active ingredient to provide a dose of about lOOng/kg to about 50mg/kg, preferably about lO ⁇ g/kg to about 5mg/kg, of the compound to the subject.
- Any of the conventional dosage forms may be used, such as tablets, lozenges, parenteral formulations, syrups, creams, ointments, aerosol formulations, transdermal patches, transmucosal patches and the like.
- the compounds of the invention can be administered as the single therapeutic agent in the treatment regimen, or the compounds of the invention may be administered in combination with one another or with other active agents, including additional immune response modifiers, antivirals, antibiotics, etc.
- the compounds of the invention have been shown to induce the production of certain cytokines in experiments performed according to the tests set forth below. These results indicate that the compounds are useful as immune response modifiers that can modulate the immune response in a number of different ways, rendering them useful in the treatment of a variety of disorders.
- Cytokines whose production may be induced by the administration of compounds according to the invention generally include interferon- (IFN- ⁇ ) and/or tumor necrosis factor- ⁇ (TNF- ⁇ ) as well as certain interleukins (IL). Cytokines whose biosynthesis may be induced by compounds of the invention include IFN- ⁇ , TNF- ⁇ , IL-1, IL-6, IL-10 and IL-12, and a variety of other cytokines. Among other effects, these and other cytokines can inhibit virus production and tumor cell growth, making the compounds useful in the treatment of viral diseases and tumors. Accordingly, the invention provides a method of inducing cytokine biosynthesis in an animal comprising administering an effective amount of a compound or composition of the invention to the animal.
- Certain compounds of the invention have been found to preferentially induce the expression of IFN- ⁇ in a population of hematopoietic cells such as PBMCs (peripheral blood mononuclear cells) containing pDC2 cells (precursor dendritic cell-type 2) without concomitant production of significant levels of inflammatory cytokines.
- PBMCs peripheral blood mononuclear cells
- pDC2 cells precursor dendritic cell-type 2
- the compounds of the invention affect other aspects of the innate immune response. For example, natural killer cell activity may be stimulated, an effect that may be due to cytokine induction.
- the compounds may also activate macrophages, which in turn stimulate secretion of nitric oxide and the production of additional cytokines. Further, the compounds may cause proliferation and differentiation of B-lymphocytes.
- Compounds of the invention also have an effect on the acquired immune response.
- the production of the T helper type 1 (Thl) cytokine IFN- ⁇ is induced indirectly and the production of the T helper type 2 (Th2) cytokines IL-4, IL-5 and IL-13 are inhibited upon administration of the compounds.
- This activity means that the compounds are useful in the treatment of diseases where upregulation of the Thl response and/or downregulation of the Th2 response is desired.
- the compounds are expected to be useful in the treatment of atopic diseases, e.g., atopic dermatitis, asthma, allergy, allergic rhinitis; systemic lupus erythematosis; as a vaccine adjuvant for cell mediated immunity; and possibly as a treatment for recurrent fungal diseases and chlamydia.
- atopic diseases e.g., atopic dermatitis, asthma, allergy, allergic rhinitis; systemic lupus erythematosis; as a vaccine adjuvant for cell mediated immunity; and possibly as a treatment for recurrent fungal diseases and chlamydia.
- the immune response modifying effects of the compounds make them useful in the treatment of a wide variety of conditions. Because of their ability to induce the production of cytokines such as IFN- ⁇ and/or TNF- ⁇ , the compounds are particularly useful in the treatment of viral diseases and tumors.
- This immunomodulating activity suggests that compounds of the invention are useful in treating diseases such as, but not limited to, viral diseases including genital warts; common warts; plantar warts; Hepatitis B; Hepatitis C; Herpes Simplex Virus Type I and Type II; molluscum contagiosum; variola, particularly variola major; rhinovirus; adenovirus; influenza; para-influenza; HIV;
- diseases such as, but not limited to, viral diseases including genital warts; common warts; plantar warts; Hepatitis B; Hepatitis C; Herpes Simplex Virus Type I and Type II; molluscum contagiosum; variola, particularly variola major; rhinovirus; adenovirus; influenza; para-influenza; HIV;
- CMV CMV
- VZV intraepithelial neoplasias such as cervical intraepithelial neoplasia; human papillomavirus (HPV) and associated neoplasias; fungal diseases, e.g.
- Candida aspergillus, and cryptococcal meningitis
- neoplastic diseases e.g., basal cell carcinoma, hairy cell leukemia, Kaposi's sarcoma, renal cell carcinoma, squamous cell carcinoma, myelogenous leukemia, multiple myeloma, melanoma, non-Hodgkin's lymphoma, cutaneous T-cell lymphoma, and other cancers
- parasitic diseases e.g., basal cell carcinoma, hairy cell leukemia, Kaposi's sarcoma, renal cell carcinoma, squamous cell carcinoma, myelogenous leukemia, multiple myeloma, melanoma, non-Hodgkin's lymphoma, cutaneous T-cell lymphoma, and other cancers
- parasitic diseases e.g.
- Additional diseases or conditions that can be treated using the compounds of the invention include actinic keratosis; eczema; eosinophilia; essential thrombocythaemia; leprosy; multiple sclerosis; Ommen's syndrome; discoid lupus; Bowen's disease; Bowenoid papulosis; alopecia areata; the inhibition of keloid formation after surgery and other types of post-surgical scars.
- these compounds could enhance or stimulate the healing of wounds, including chronic wounds.
- the compounds may be useful for treating the opportunistic infections and tumors that occur after suppression of cell mediated immunity in, for example, transplant patients, cancer patients and HIV patients
- An amount of a compound effective to induce cytokine biosynthesis is an amount sufficient to cause one or more cell types, such as monocytes, macrophages, dendritic cells and B-cells to produce an amount of one or more cytokines such as, for example, IFN- ⁇ , TNF- ⁇ , IL-1, IL-6, IL-10 and IL-12 that is increased over the background level of such cytokines.
- the precise amount will vary according to factors known in the art but is expected to be a dose of about 100 ng/kg to about 50 mg/kg, preferably about 10 ⁇ g/kg to about 5 mg/kg.
- the invention also provides a method of treating a viral infection in an animal and a method of treating a neoplastic disease in an animal comprising administering an effective amount of a compound or composition of the invention to the animal.
- An amount effective to treat or inhibit a viral infection is an amount that will cause a reduction in one or more of the manifestations of viral infection, such as viral lesions, viral load, rate of virus production, and mortality as compared to untreated control animals.
- the precise amount will vary according to factors known in the art but is expected to be a dose of about 100 ng/kg to about 50 mg/kg, preferably about 10 ⁇ g/kg to about 5 mg/kg.
- An amount of a compound effective to treat a neoplastic condition is an amount that will cause a reduction in tumor size or in the number of tumor foci. Again, the precise amount will vary according to factors known in the art but is expected to be a dose of about 100 ng/kg to about 50 mg/kg, preferably about 10 ⁇ g/kg to about 5 mg/kg.
- aqueous fraction was then extracted multiple times with dichloromethane.
- the organic fractions were combined, dried over magnesium sulfate, filtered and then concentrated under reduced pressure to provide 18.5 g of l-[2-(2-pro ⁇ ynyloxy)ethyl]-lH-imidazo[4,5-c]quinoline-5N- oxide as a yellow oil.
- Trifluoroacetic acid (20 mL) was added to a solution of the material from Part B in dichloromethane (20 mL). After 4 hours the reaction mixture was diluted with dichloromethane containing a small amount of methanol and 20% sodium hydroxide. The layers were separated. The aqueous fraction was extracted with dichloromethane. The organic fractions were combined, dried over magnesium sulfate, filtered and then concentrated under reduced pressure to provide a yellow powder. This material was purified by flash chromatography eluting with 9/1 dichloromethane/methanol to provide
- reaction mixture (0.05 g, 0.26 mmol) were added and the reaction mixture was stirred for 1 hour at ambient temperature at which time analysis by ⁇ PLC (reverse phase, acetonitrile/water) indicated that the reaction was complete.
- ⁇ PLC reverse phase, acetonitrile/water
- the aqueous fraction was extracted with dichloromethane. The organic fractions were combined, dried over magnesium sulfate and then concentrated to a volume of ⁇ 10 mL. The concentrate was allowed to stand over the weekend and then it was diluted with toluene. The resulting precipitate was isolated by filtration and identified as starting material. The filtrate was diluted with diethyl ether. The resulting precipitate was isolated by filtration to provide 1.1 g of benzyl N- ⁇ l-[2- (propynyloxy)ethyl]-lH-imidazo[4,5-c]quinolin-4-yl ⁇ carbamate as a white solid.
- This material was further purified by column chromatography eluting with 99/1 ethyl acetate/methanol to provide 24 mg of 1 -(2- ⁇ [3-(4-phenoxyphenyl)-2-propynyl]oxy ⁇ ethyl)-lH-imidazo[4,5- c]quinolin-4-amine as a solid, m.p. 146-148°C.
- This material was partially dissolved in a mixture of dichloromethane (17 mL) and methanol (17 mL). Hydrogen chloride/diethyl ether (3.24 L of 1.0 M) was added and the mixture turned homogeneous. The mixture was concentrated under reduced pressure to provide a brown crystalline residue. The residue was combined with 50/50 acetonitrile/ethyl acetate containing a small amount of methanol. Sodium hydroxide (0.5 mL of 20%) was added. The mixture was concentrated under reduced pressure to provide a glassy solid.
- dibenzyl dicarbonate 50 g, 174 mmol was added to a mixture of l-[2-(2-propynyloxy)ethyl]-lH-imidazo[4,5-c]quinolin-4-amine (16.4 g, 61.6 mmol) and anhydrous N,N-dimethylformamide (200 mL).
- the reaction mixture was allowed to stir at ambient temperature for 16 hours and the reaction mixture turned homogeneous.
- the reaction mixture was partitioned between ethyl acetate and water. The layers were separated. The aqueous layer was extracted with ethyl acetate.
- N,N-(bis benzyloxycarbonyl)- 1-[2-(2- propynyloxy)ethylj-lH-imidazo[4,5-c]quinolin-4-amine 0.5 g, 0.94 mmol
- anhydrous acetonitrile 5 mL
- triethylamine 0.34 mL, 2.43 mmol
- l-(4-iodophenyl)pyrrole (0.28 g, 1.03 mmol) were combined and the resulting homogeneous mixture was heated to
- This material was purified on a second column using 9/1 hexane/ethyl acetate to provide 0.229 g of N,N-(bis benzyloxycarbonyl)- l-[2-( ⁇ 3-[4-(lH-pyrrol-l-yl)phenyl]prop-2- ynyl ⁇ oxy)ethyl]-lH-imidazo[4,5-c]quinolin-4-amine.
- N,N-(bis tert-butoxycarbonyl)- 1-[2-(2- propynyloxy)ethyl]-lH-imidazo[4,5-c]quinolin-4-amine (2.82 g g, 6.04 mmol)
- benzyl 3- iodobenzoate 2.245 g, 6.64 mmol
- triethylamine 2.2 mL, 15.7 mmol
- anhydrous acetonitrile (20 mL) were combined and the resulting mixture was heated to 60°C.
- Copper (I) iodide (0.05 g) and dichlorobis(triphenylphosphine)palladium(II) (0.0.08 g) were added.
- Example 13 2- ⁇ 3 -[2-(4-Amino- 1 H-imidazo [4, 5 -cjquinolin- 1 -yl)ethoxy]propyl ⁇ benzoic acid trifluoroacetate
- Example 12 Part B Using the general method of Example 12 Part B, the material from Part A was hydrogenated to provide 0.041 g of a mixture of mono-and di-BOC protected 2- ⁇ 3-[2-(4- amino-lH-imidazo[4,5-c]quinolin-l-yl)ethoxy]propyl ⁇ benzoic acid.
- Example 12 Part C the material from Part B was hydrolyzed to provide 0.28 g of 2- ⁇ 3-[2-(4-amino-lH-imidazo[4,5-c]quinolin-l- yl)ethoxy]propyl ⁇ benzoic acid as a solid, m.p. 186-188°C. Analysis. Calculated for C 22 ⁇ 2 2N 4 03»C 2 ⁇ F 3 0 2 : %C, 57.14; %H, 4.59; %N, 11.11.
- Example 12 Part B Using the general method of Example 12 Part B, the material from Part A was hydrogenated to provide 1.86 g of a mixture of mono-and di-BOC protected 4- ⁇ 3-[2-(4- amino-lH-imidazo[4,5-c]quinolin-l-yl)ethoxy]propyl ⁇ benzoic acid.
- Example 12 Part C Using the general method of Example 12 Part C, the material from Part B was hydrolyzed to provide 0.96 g of 4- ⁇ 3-[2-(4-amino-lH-imidazo[4,5-c]quinolin-l- yl)ethoxy]propyl ⁇ benzoic acid trifluoroacetate, m.p. 235-237°C.
- Example 12 Part B Using the general method of Example 12 Part B, the material from Part A was hydrogenated to provide -2.9 g of a mixture of mono Boc protected and unprotected l-(2- ⁇ 3-[3-(dimethylamino)phenyl]propoxy ⁇ ethyl)-lH-imidazo[4,5-c]quinolin-4-amine.
- the material from Part B was combined with hydrogen chloride/methanol (30 mL of 3 M) and stirred at ambient temperature for 19 hours. A precipitate was removed by filtration. The filtrate was concentrated under reduced pressure and the residue was dissolved in a small amount of methanol and then neutralized with concentrated ammonium hydroxide to p ⁇ ⁇ 11. The resulting precipitate was purified by column chromatography eluting with 95/5/1 dichloromethane/methanol/ammonium hydroxide. This material was combined with hydrogen chloride/diethyl ether. The resulting solution was concentrated under reduced pressure. The residue was triturated with diethyl ether.
- the resulting solution was heated to 80°C.
- 2-iodoaniline (0.26 mL, 1.18 mmol
- copper (I) iodide 0.012 g
- dichlorobis(triphenylphosphine)palladium(II) 0.023 g
- Catalyst (5% platinum on carbon) was added to a solution of N,N-(bis tert- butoxycarbonyl)-! -(2- ⁇ [3-(2-aminophenyl)prop-2-ynyl]oxy ⁇ ethyl)-lH-imidazo[4,5- c]quinolin-4-amine in methanol.
- the mixture was hydrogenated on a Parr apparatus at 50 psi (3.5 Kg.cm 2 ) overnight.
- the reaction mixture was filtered through a layer of Celite® filter aid and the filter cake was washed with additional methanol. The filtrate was concentrated under reduced pressure to provide an off-white solid.
- Examples 24 - 27 The compounds in the table below were prepared according to the synthetic method of Reaction Scheme I above using the following general method. 2-(4-Amino-lH ⁇ imidazo[4,5-c]quinolin-l-yl)-2-ethylethanol (25 mg) was placed in a 2 dram (7.4 mL) vial. Sodium hydride (1.75 eq of 60% in mineral oil) and N,N- dimethylformamide (1 mL) were added. The vial was placed on a sonicator for about 10 minutes at ambient temperature to allow the alkoxide to form. The halide (1.75 eq) was added and the vial was placed back on the sonicator for about 30 to 60 minutes at ambient temperature.
- the reaction mixture was analyzed by LC/MS to confirm the formation of the desired product.
- the reaction mixture was purified by semi-preparative ⁇ PLC.
- the semi-prep ⁇ PLC fractions were analyzed by LC-APCI/MS and the appropriate fractions were combined and lyophilized to provide the trifluoroacetate salt of the desired product, which was confirmed by accurate mass and ⁇ NMR.
- the table below shows the structure of the free base and the theoretical mass (TM) and the measured mass (MM).
- the 4-amino-lH-imidazo[4,5-c]quinolin-l-yl alcohol (25 mg) was placed in a 2 dram (7.4 mL) vial.
- the vial was placed on a sonicator for about 1 hour at 50°C to allow the alkoxide to form.
- the halide (1.2 eq) was added and the vial was placed back on the sonicator for about 1 to 2 hours at 50°C.
- the reaction mixture was analyzed by LC/MS to confirm the formation of the desired product.
- the reaction mixture was purified by semi-preparative ⁇ PLC.
- the semi-prep ⁇ PLC fractions were analyzed by LC-APCI/MS and the appropriate fractions were combined and lyophilized to provide the trifluoroacetate salt of the desired product, which was confirmed by accurate mass and ⁇ NMR.
- the table below shows the structure of the free base and the theoretical mass (TM) and the measured mass (MM).
- the 4-amino-lH-imidazo[4,5-c]quinolin-l-yl alcohol (25 mg) was placed in a 2 dram (7.4 mL) vial.
- the vial was placed on a sonicator for about 15 to 30 minutes at ambient temperature to allow the alkoxide to form.
- the halide (1.2 eq) was added and the vial was placed back on the sonicator for about 15 to 120 minutes at ambient temperature.
- the reaction mixture was analyzed by LC/MS to confirm the formation of the desired product.
- the reaction mixture was purified by semi-preparative ⁇ PLC.
- the semi-prep ⁇ PLC fractions were analyzed by LC-APCI/MS and the appropriate fractions were combined and lyophilized to provide the trifluoroacetate salt of the desired product, which was confirmed by accurate mass and ⁇ NMR.
- the table below shows the structure of the free base and the theoretical mass (TM) and the measured mass (MM) or nominal mass (NM).
- the reaction mixture was purified by semi-preparative ⁇ PLC.
- the semi-prep ⁇ PLC fractions were analyzed by LC-APCI/MS and the appropriate fractions were combined and lyophilized to provide the trifluoroacetate salt of the desired product , which was confirmed by accurate mass and ⁇ NMR.
- the table below shows the structure of the free base and the theoretical mass (TM) and the measured mass (MM).
- the reaction mixture was sonicated for about 30 minutes and then shaken overnight at ambient temperature.
- the reaction mixture was purified by semi-preparative ⁇ PLC using Method A.
- the compounds of Examples 99 and 100 were provided as the trifluoroacetate salts
- the products were confirmed by accurate mass and ⁇ NMR.
- the table below shows the structure of the free base and the theoretical mass (TM) and the nominal mass (NM).
- (2R)-2-[(3-Aminoquinolin-4-yl)amino]butan-l-ol (416.0 g, 1 eq.) and triethylorthoformate (1.2 L, 4 eq.) were combined and slowly heated to 145°C. Ethanol was distilled off as it formed during the reaction. After -500 mL of ethanol had been distilled off, the reaction mixture was allowed to cool to 50°C under a nitrogen atmosphere. Excess triethyLorthoformate was removed under reduced pressure to provide crude (2R)-2-( 1 H-imidazo [4, 5-c] quinolin- 1 -yl)butan- 1 -ol .
- 3-Chloroperoxybenzoic acid (15.0 g of 57-86%) was added to a chilled (0°) mixture of the material from Part F and chloroform (250 mL). After 0.5 hour the reaction mixture was allowed to warm to ambient temperature. The progress of the reaction was monitored by TLC and two additional portions of 3-chloroperoxybenzoic acid (3.75 g) were added. When the reaction was complete, it was washed with sodium bicarbonate. The aqueous fraction was extracted with ethyl acetate.
- Trichloroacetyl isocyanate (10.7 mL) was added dropwise to a mixture of the material from Part G and anhydrous dichloromethane (300 mL). After 1 hour analysis by TLC indicated that the reaction was not complete so more trichloroacetyl isocyanate (2 mL) was added. After 1 hour the reaction mixture was concentrated under reduced pressure to provide 2,2,2-trichloro-N-(l- ⁇ (lR)-l-[(2-propynyloxy)methyl]propyl ⁇ -lH- imidazo[4,5-c]quinolin-4-yl)acetamide as a yellow solid.
- Examples 110 - 112 Part A Triethylamine (15 mL) and R-3-amino-2-methylpropan-l-ol (about 0.1 mole of crude) were added to a solution of 2,4-dichloro-3-nitroquinoline (24.3 g, 0.1 mole) in dichloromethane (250 mL). The reaction mixture was refluxed until analysis by TLC showed no change. The reaction mixture was evaporated to dryness. The solid yellow- brown residue was crushed and then extracted repeatedly with hexane containing a small amount of dichloromethane in order to remove the starting quinoline.
- the reaction mixture was purified by semi-preparative HPLC.
- the semi-prep HPLC fractions were analyzed by LC-APCI/MS and the appropriate fractions were combined and lyophilized to provide the trifluoroacetate salt of the desired product, which was confirmed by accurate mass and ⁇ NMR.
- the table below shows the structure of the free base and the theoretical mass (TM) and the measured mass (MM).
- This material was slurried with refluxing ethyl acetate (-5 mL). The mixture was cooled and a precipitate was isolated by filtration. The filtrate was concentrated under reduced pressure. The resulting residue was slurried twice with ethyl acetate and then combined with the precipitate to provide 0.8 g of solid. This solid was recrystallized from ethanol ( ⁇ 5 mL) to provide 0.6 g of l-[(benzyloxy)methyl]-lH-imidazo[4,5-c]quinolin-4- amine, m.p. 168-172°C.
- 3-methoxypropanoyl chloride (0.86 ml, 7.9 mmol) was added dropwise over a 30 minute period to a chilled (ice bath) solution of N 4 -(2-phenoxyethyl)quinoline-3,4-diamine (2.0 g, 7.2 mmol) in dichloromethane (100 ml). After a few hours, a precipitate formed. The solvent volume was reduced under vacuum to near dryness and hexane (100 ml) was added. Vacuum filtration provided 2.9 g of 3-methoxy-N- ⁇ 4-[(2- phenoxyethyl)amino]quinolin-3-yl ⁇ propanamide as a hydrochloride salt.
- 3-Chloroperoxybenzoic acid (1.5 g, 8.7 mmol, 60% by weight) was added in three portions over a period of 20 minutes to 2-(2-methoxyethyl)-l-(2-phenoxyethyl)-lH- imidazo[4,5-c]quinoline (1.8 g, 5.2 mmol) in chloroform (100 ml).
- the reaction mixture was maintained at ambient temperature overnight and then washed with saturated sodium bicarbonate followed by water.
- the organic fraction was dried (MgS0 4 ) and concentrated under vacuum to near dryness.
- N 4 -(2-Phenoxyethyl)quinoline-3,4-diamine (1.5 g, 5.4 mmol) and isovaleryl chloride (0.8 ml, 6.4 mmol) were combined and treated according to the general procedures of Parts C-E of Example 129.
- the reaction was chilled (ice bath) and -toluenesulfonyl chloride (0.85 g, 4.5 mmol) was slowly added over a period of 20 minutes. The cooling bath was removed and the reaction was maintained at ambient temperature overnight. The phases were separated and the organic phase was sequentially washed with 1% aqueous sodium carbonate (3X), water, brine; dried (Na 2 S0 ); and concentrated to near dryness in vacuo. Hexane was added to provide a precipitate.
- N 4 -(2-Phenoxyethyl)quinoline-3,4-diamine (2.0 g, 7.2 mmol) and isobutyryl chloride (0.9 ml, 8.6 mmol) were combined and treated according to the general procedure described in Example 130. Recrystallization from acetonitrile provided 0.82 g of 2- isopropyl-l-(2-phenoxyethyl)-lH-imidazo[4,5-c]quinolin-4-amine as a tan solid, m.p. 229-231°C.
- N 4 -(2-Phenoxyethyl)quinoline-3,4-diamine (2.0 g, 7.2 mmol), xylenes (150 ml), and trimethylorthovalerate (2.5 ml, 14.3 mmol) were combined under an atmosphere of nitrogen and heated at reflux temperature for 4 days. The external heat was increased and approximately 35 ml of xylenes was removed by distillation. The reaction was slowly cooled to room temperature and a precipitate formed. The solid was recovered by vacuum filtration to yield 2.4 g of 2-butyl-l-(2-phenoxyethyl)-lH-imidazo[4,5-c]quinoline as a light tan crystalline solid.
- N 4 -(2-phenoxyethyl)quinoline-3,4-diamine (2.0 g, 7.2 mmol) and cyclopentanecarbonyl chloride (1.1 ml, 8.6 mmol) were combined and treated according to the general procedure described in Example 130. Recrystallization from acetonitrile provided 1.4 g of 2-cyclopentyl-l-(2-phenoxyethyl)-lH-imidazo[4,5-c]quinolin-4-amine as a tan solid, m.p. 216.0-217.9°C.
- N 4 -(2-phenoxyethyl)quinoline-3,4-diamine (2.0 g, 7.2 mmol) and 2-(2- methoxyethoxy)acetyl chloride (1.3 g, 8.6 mmol) were combined and treated according to the general procedure described in Example 130. Recrystallization from methanol provided 1.6 g of 2-[(2-methoxyethoxy)methyl]-l-(2-phenoxyethyl)-lH-imidazo[4,5- c]quinolin-4-amine as white needles, m.p. 170.0-171.5°C.
- N 4 -(2-phenoxyethyl)quinolme-3,4-diamine (1.7 g, 6.1 mmol) and cyclopropylacetyl chloride (0.86 ml, 7.3 mmol) were combined and treated according to the general procedure described in Example 130. Recrystallization from methanol provided 0.86 g of 2-(cyclopropylmethyl)-l-(2-phenoxyethyl)-lH-imidazo[4,5-c]quinolin- 4-amine as a white solid, m.p. 191.7-192.6°C.
- N 4 -(2-phenoxyethyl)quinoline-3,4-diamine (1.6 g, 5.7 mmol) and tetrahydrofuran- 3-carbonyl chloride (0.98 ml, 7.3 mmol) were combined and treated according to the general procedure described in Example 130. Recrystallization from acetonitrile provided 0.3 g of l-(2-phenoxyethyl)-2-tetrahydrofuran-3-yl-lH-imidazo[4,5-c]quinolin-4-amine as a tan solid, m.p. 235.9-236.3°C.
- reaction became a dark orange solution. After 1.5 hours the reaction was quenched by the slow addition of saturated ammonium chloride solution (10 ml). The methanol was removed in vacuo. The aqueous residue was extracted with dichloromethane (3 x 10 ml) and the organic fractions were combined and washed with water (10 ml) and brine (10 ml). The solution was dried (Na 2 S0 4 ), filtered and concentrated in vacuo to yield the crude product as an orange solid.
- Example 115 Part C Using the general method of Example 115 Part C, the 4-amino group was introduced to 2-(2-methyl-5-oxido-lH-imidazo[4,5-c]quinolin-l-yl)ethyl acetate (8.47 g, 29.71 mmol). The resulting brown oil was purified by trituration with acetonitrile and dried to yield 3.583 g of 2-(4-amino-2-methyl-lH-imidazo[4,5-c]quinolin-l-yl)ethyl acetate as a tan solid.
- the resulting oil was partitioned between dichloromethane and 4% aqueous sodium carbonate and the organic layer removed.
- the aqueous layer was extracted with dichloromethane (3x).
- the organic fractions were combined, dried with anhydrous sodium sulfate and the volatiles were removed under reduced pressure.
- the resulting oil was purified by chromatography over silica gel (95/5 dichloromethane/methanol).
- the resulting white solid was dissolved in dichloromethane (2 mL) and reacted with IM HCl in ether (2 mL).
- the volatiles were removed under reduced pressure and the resulting solids recrystallized from methanol to provide 0.1089 g of 2-methyl-l- ⁇ 2-[(3-phenylprop-2-ynyl)oxy]ethyl ⁇ -
- cytokine induction An in vitro human blood cell system is used to assess cytokine induction. Activity is based on the measurement of interferon and tumor necrosis factor ( ⁇ ) (IFN and TNF, respectively) secreted into culture media as described by Testerman et. al. In “Cytokine Induction by the Immunomodulators Imiquimod and S-27609", Journal of Leukocyte Biology, 58, 365-372 (September, 1995).
- ⁇ interferon and tumor necrosis factor
- PBMCs Peripheral blood mononuclear cells
- Histopaque®-1077 The PBMCs are washed twice with Hank's Balanced Salts Solution and then are suspended at 3-4 x 10 6 cells/mL in RPMI complete.
- the PBMC suspension is added to 48 well flat bottom sterile tissue culture plates (Costar, Cambridge, MA or Becton Dickinson Labware, Lincoln Park,
- the compounds are solubilized in dimethyl sulfoxide (DMSO).
- DMSO dimethyl sulfoxide
- the DMSO concentration should not exceed a final concentration of 1% for addition to the culture wells.
- test compound is added at 60 ⁇ M to the first well containing RPMI complete and serial 3 fold dilutions are made in the wells.
- the PBMC suspension is then added to the wells in an equal volume, bringing the test compound concentrations to the desired range (0.12 to 30 ⁇ M).
- the final concentration of PBMC suspension is 1.5-2 X
- Interferon ( ⁇ ) concentration is determined by ELISA using a Human Multi-Species kit from PBL Biomedical Laboratories, New Brunswick, NJ. Results are expressed in pg/mL.
- Tumor necrosis factor ( ⁇ ) concentration is determined using ELISA kits available from Genzyme, Cambridge, MA; R&D Systems, Minneapolis, MN; or Pharmingen, San
- the table below lists the lowest concentration found to induce interferon and the lowest concentration found to induce tumor necrosis factor for each compound. A "*" indicates that no induction was seen at any of the tested concentrations; generally the highest concentration tested was 10 or 30 ⁇ M.
Abstract
Description
Claims
Priority Applications (17)
Application Number | Priority Date | Filing Date | Title |
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UA2003065277A UA75622C2 (en) | 2000-12-08 | 2001-06-12 | Aryl ether substituted imidazoquinolines, pharmaceutical composition based thereon |
HU0700062A HUP0700062A2 (en) | 2000-12-08 | 2001-12-06 | Aryl ether substituted imidazoquinolines and pharmaceutical compositions thereof |
NZ526105A NZ526105A (en) | 2000-12-08 | 2001-12-06 | Aryl ether substituted imidazoquinolines as immunomodulators, for inducing cytokine biosynthesis |
AU3951602A AU3951602A (en) | 2000-12-08 | 2001-12-06 | Aryl ether substituted imidazoquinolines |
BRPI0116052-4A BR0116052A (en) | 2000-12-08 | 2001-12-06 | imidazoquinolines substituted by aryl ether |
AU2002239516A AU2002239516B2 (en) | 2000-12-08 | 2001-12-06 | Aryl ether substituted imidazoquinolines |
CA002430844A CA2430844A1 (en) | 2000-12-08 | 2001-12-06 | Aryl ether substituted imidazoquinolines |
JP2002547926A JP2004523498A (en) | 2000-12-08 | 2001-12-06 | Aryl ether substituted imidazoquinoline |
EEP200300270A EE200300270A (en) | 2000-12-08 | 2001-12-06 | Aryl ether substituted imidazoquinolines |
PL01366115A PL366115A1 (en) | 2000-12-08 | 2001-12-06 | Aryl ether substituted imidazoquinolines |
KR10-2003-7007538A KR20040028691A (en) | 2000-12-08 | 2001-12-06 | Aryl Ether Substituted Imidazoquinolines |
SK684-2003A SK6842003A3 (en) | 2000-12-08 | 2001-12-06 | Aryl ether substituted imidazoquinolines |
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NO20032452A NO20032452L (en) | 2000-12-08 | 2003-05-28 | Aryl ether substituted imidazole quinolines |
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PCT/US2001/046359 WO2002046188A2 (en) | 2000-12-08 | 2001-12-06 | Amido ether substituted imidazoquinolines |
PCT/US2001/046696 WO2002046191A2 (en) | 2000-12-08 | 2001-12-06 | Urea substituted imidazoquinoline ethers |
PCT/US2001/046704 WO2002046193A2 (en) | 2000-12-08 | 2001-12-06 | Heterocyclic ether substituted imidazoquinolines |
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PCT/US2001/046704 WO2002046193A2 (en) | 2000-12-08 | 2001-12-06 | Heterocyclic ether substituted imidazoquinolines |
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JP2009514850A (en) | 2005-11-04 | 2009-04-09 | ノバルティス ヴァクシンズ アンド ダイアグノスティクス エスアールエル | Influenza vaccine with reduced amount of oil-in-water emulsion as adjuvant |
EP1951299B1 (en) | 2005-11-04 | 2012-01-04 | Novartis Vaccines and Diagnostics S.r.l. | Influenza vaccines including combinations of particulate adjuvants and immunopotentiators |
WO2007085969A2 (en) | 2006-01-27 | 2007-08-02 | Novartis Vaccines And Diagnostics Gmbh & Co Kg | Influenza vaccines containing hemagglutinin and matrix proteins |
WO2007100634A2 (en) | 2006-02-22 | 2007-09-07 | 3M Innovative Properties Company | Immune response modifier conjugates |
WO2007106854A2 (en) * | 2006-03-15 | 2007-09-20 | Coley Pharmaceutical Group, Inc. | Hydroxy and alkoxy substituted 1h-imidazonaphthyridines and methods |
WO2007109812A2 (en) * | 2006-03-23 | 2007-09-27 | Novartis Ag | Immunopotentiating compounds |
EP2357184B1 (en) | 2006-03-23 | 2015-02-25 | Novartis AG | Imidazoquinoxaline compounds as immunomodulators |
CA2647100A1 (en) * | 2006-03-23 | 2007-09-27 | Novartis Ag | Methods for the preparation of imidazole-containing compounds |
EP2004226A1 (en) | 2006-03-24 | 2008-12-24 | Novartis Vaccines and Diagnostics GmbH & Co. KG | Storage of influenza vaccines without refrigeration |
SG173336A1 (en) | 2006-03-31 | 2011-08-29 | Novartis Ag | Combined mucosal and parenteral immunization against hiv |
ATE522541T1 (en) | 2006-06-09 | 2011-09-15 | Novartis Ag | BACTERIAL ADHESIN CONFORMERS |
US7906506B2 (en) | 2006-07-12 | 2011-03-15 | 3M Innovative Properties Company | Substituted chiral fused [1,2] imidazo [4,5-c] ring compounds and methods |
GB0614460D0 (en) | 2006-07-20 | 2006-08-30 | Novartis Ag | Vaccines |
CA2659552A1 (en) | 2006-08-16 | 2008-02-21 | Novartis Ag | Immunogens from uropathogenic escherichia coli |
WO2008030511A2 (en) | 2006-09-06 | 2008-03-13 | Coley Pharmaceuticial Group, Inc. | Substituted 3,4,6,7-tetrahydro-5h, 1,2a,4a,8-tetraazacyclopenta[cd]phenalenes |
US20100010199A1 (en) | 2006-09-11 | 2010-01-14 | Novartis Ag | Making influenza virus vaccines without using eggs |
WO2008068631A2 (en) | 2006-12-06 | 2008-06-12 | Novartis Ag | Vaccines including antigen from four strains of influenza virus |
US20080149123A1 (en) * | 2006-12-22 | 2008-06-26 | Mckay William D | Particulate material dispensing hairbrush with combination bristles |
GB0700562D0 (en) | 2007-01-11 | 2007-02-21 | Novartis Vaccines & Diagnostic | Modified Saccharides |
PL2185191T3 (en) | 2007-06-27 | 2013-02-28 | Novartis Ag | Low-additive influenza vaccines |
GB0714963D0 (en) | 2007-08-01 | 2007-09-12 | Novartis Ag | Compositions comprising antigens |
GB0810305D0 (en) | 2008-06-05 | 2008-07-09 | Novartis Ag | Influenza vaccination |
GB0818453D0 (en) | 2008-10-08 | 2008-11-12 | Novartis Ag | Fermentation processes for cultivating streptococci and purification processes for obtaining cps therefrom |
EA018579B1 (en) * | 2008-01-15 | 2013-09-30 | Меда Аб | Method of treatment of polypes/polyposis and precancerous colorectal changes |
CA2716706C (en) | 2008-03-03 | 2014-02-18 | Irm Llc | Compounds and compositions as tlr activity modulators |
NZ587798A (en) | 2008-03-18 | 2013-06-28 | Novartis Ag | Improvements in the preparation of influenza virus vaccine antigens utilising a phosphate buffer |
JP2012519482A (en) | 2009-03-06 | 2012-08-30 | ノバルティス アーゲー | Chlamydia antigen |
EP2419129A2 (en) | 2009-04-14 | 2012-02-22 | Novartis AG | Compositions for immunising against staphylococcus aerus |
FR2949344A1 (en) | 2009-04-27 | 2011-03-04 | Novartis Ag | FLU PROTECTIVE VACCINES |
AU2013203591B2 (en) * | 2009-05-01 | 2017-01-19 | University Court Of The University Of Dundee | Treatment or prophylaxis of proliferative conditions |
GB0907551D0 (en) * | 2009-05-01 | 2009-06-10 | Univ Dundee | Treatment or prophylaxis of proliferative conditions |
AR077757A1 (en) | 2009-07-15 | 2011-09-21 | Novartis Ag | COMPOSITIONS OF FUSION PROTEINS OF RESPIRATORY SINCICIAL VIRUS (RSV) AND METHODS FOR PREPARATION |
EP2464658B1 (en) | 2009-07-16 | 2014-10-01 | Novartis AG | Detoxified escherichia coli immunogens |
GB0918392D0 (en) | 2009-10-20 | 2009-12-02 | Novartis Ag | Diagnostic and therapeutic methods |
GB0919690D0 (en) | 2009-11-10 | 2009-12-23 | Guy S And St Thomas S Nhs Foun | compositions for immunising against staphylococcus aureus |
GB201009861D0 (en) | 2010-06-11 | 2010-07-21 | Novartis Ag | OMV vaccines |
PL2606047T3 (en) | 2010-08-17 | 2017-07-31 | 3M Innovative Properties Company | Lipidated immune response modifier compound compositions, formulations, and methods |
ES2575688T3 (en) | 2010-12-16 | 2016-06-30 | Sumitomo Dainippon Pharma Co., Ltd. | Imidazo [4,5-c] quinolin-1-yl derivative useful in therapy |
EP4144368A1 (en) | 2011-01-26 | 2023-03-08 | GlaxoSmithKline Biologicals S.A. | Rsv immunization regimen |
ES2782119T3 (en) | 2011-05-13 | 2020-09-10 | Glaxosmithkline Biologicals Sa | RSV prefusion F antigens |
US8728486B2 (en) | 2011-05-18 | 2014-05-20 | University Of Kansas | Toll-like receptor-7 and -8 modulatory 1H imidazoquinoline derived compounds |
CA2838158C (en) | 2011-06-03 | 2019-07-16 | 3M Innovative Properties Company | Heterobifunctional linkers with polyethylene glycol segments and immune response modifier conjugates made therefrom |
MX355623B (en) * | 2011-06-03 | 2018-04-25 | 3M Innovative Properties Co | Hydrazino 1h-imidazoquinolin-4-amines and conjugates made therefrom. |
AU2012335208B2 (en) | 2011-11-07 | 2017-08-31 | Glaxosmithkline Biologicals S.A. | Carrier molecule comprising a spr0096 and a spr2021 antigen |
WO2013108272A2 (en) | 2012-01-20 | 2013-07-25 | International Centre For Genetic Engineering And Biotechnology | Blood stage malaria vaccine |
CN112587658A (en) | 2012-07-18 | 2021-04-02 | 博笛生物科技有限公司 | Targeted immunotherapy for cancer |
DK2941233T3 (en) | 2013-01-07 | 2020-10-19 | Univ Pennsylvania | Compositions and methods for treating cutaneous T-cell lymphoma |
JP6446054B2 (en) | 2013-11-05 | 2018-12-26 | スリーエム・イノベイティブ・プロパティーズ・カンパニー | Sesame oil-based injection formulation |
EP2870974A1 (en) | 2013-11-08 | 2015-05-13 | Novartis AG | Salmonella conjugate vaccines |
SG11201605455YA (en) | 2014-01-10 | 2016-08-30 | Birdie Biopharmaceuticals Inc | Compounds and compositions for treating egfr expressing tumors |
EA037818B1 (en) | 2014-03-26 | 2021-05-25 | Глаксосмитклайн Байолоджикалс С.А. | Mutant staphylococcal antigens |
CN105233291A (en) | 2014-07-09 | 2016-01-13 | 博笛生物科技有限公司 | Combined therapy composition and combined therapy method for treating cancers |
AU2015286043B2 (en) | 2014-07-09 | 2020-08-20 | Birdie Biopharmaceuticals Inc. | Anti-PD-L1 combinations for treating tumors |
CN105440135A (en) | 2014-09-01 | 2016-03-30 | 博笛生物科技有限公司 | Anti-PD-L1 conjugate for treating tumors |
CN105461767B (en) * | 2014-08-07 | 2019-03-12 | 富力 | A kind of chemical synthesis process of forsythin |
KR102161364B1 (en) * | 2015-09-14 | 2020-09-29 | 화이자 인코포레이티드 | Imidazo[4,5-c]quinoline and imidazo[4,5-c][1,5]naphthyridine derivatives as LRRK2 inhibitors |
CN108770357B (en) * | 2015-09-29 | 2022-10-28 | 芝加哥大学 | Polymer conjugate vaccines |
WO2017059280A1 (en) | 2015-10-02 | 2017-04-06 | The University Of North Carolina At Chapel Hill | Novel pan-tam inhibitors and mer/axl dual inhibitors |
CN115554406A (en) | 2016-01-07 | 2023-01-03 | 博笛生物科技有限公司 | anti-CD 20 combinations for the treatment of tumors |
CN115252792A (en) | 2016-01-07 | 2022-11-01 | 博笛生物科技有限公司 | anti-EGFR combinations for the treatment of tumors |
CN106943598A (en) | 2016-01-07 | 2017-07-14 | 博笛生物科技(北京)有限公司 | Anti- HER2 for treating tumour is combined |
CN108794467A (en) | 2017-04-27 | 2018-11-13 | 博笛生物科技有限公司 | 2- amino-quinoline derivatives |
US11517567B2 (en) | 2017-06-23 | 2022-12-06 | Birdie Biopharmaceuticals, Inc. | Pharmaceutical compositions |
US11306083B2 (en) | 2017-12-20 | 2022-04-19 | 3M Innovative Properties Company | Amide substituted imidazo[4,5-C]quinoline compounds with a branched chain linking group for use as an immune response modifier |
CA3091027A1 (en) | 2018-02-02 | 2019-08-08 | Maverix Oncology, Inc. | Small molecule drug conjugates of gemcitabine monophosphate |
WO2019166937A1 (en) * | 2018-02-28 | 2019-09-06 | 3M Innovative Properties Company | Substituted imidazo[4,5-c]quinoline compounds with an n-1 branched group |
RU2020128440A (en) | 2018-02-28 | 2022-03-28 | Пфайзер Инк. | IL-15 OPTIONS AND THEIR APPLICATIONS |
JP7384835B2 (en) | 2018-05-23 | 2023-11-21 | ファイザー・インク | Antibodies specific to CD3 and their uses |
TWI816396B (en) | 2018-05-23 | 2023-09-21 | 美商輝瑞大藥廠 | Antibodies specific for gucy2c and uses thereof |
EP3802536B1 (en) | 2018-05-24 | 2022-07-13 | 3M Innovative Properties Company | N-1 branched cycloalkyl substituted imidazo[4,5-c]quinoline compounds, compositions, and methods |
US20210213010A1 (en) * | 2018-07-24 | 2021-07-15 | Torque Therapeutics, Inc. | Tlr7/8 agonists and liposome compositions |
WO2020109898A1 (en) * | 2018-11-26 | 2020-06-04 | 3M Innovative Properties Company | N-1 branched alkyl ether substituted imidazo[4,5-c]quinoline compounds, compositions, and methods |
WO2020128893A1 (en) | 2018-12-21 | 2020-06-25 | Pfizer Inc. | Combination treatments of cancer comprising a tlr agonist |
CN114616234B (en) * | 2019-02-07 | 2024-04-12 | 康威(广州)生物科技有限公司 | Phosphorus imidazoquinoline amine derivative, pharmaceutical composition and application thereof |
WO2020168017A1 (en) | 2019-02-12 | 2020-08-20 | Ambrx, Inc. | Compositions containing, methods and uses of antibody-tlr agonist conjugates |
EP4077387A1 (en) | 2019-12-17 | 2022-10-26 | Pfizer Inc. | Antibodies specific for cd47, pd-l1, and uses thereof |
PE20231565A1 (en) | 2020-07-17 | 2023-10-04 | Pfizer | THERAPEUTIC ANTIBODIES AND THEIR USES |
US20230302150A1 (en) | 2020-08-20 | 2023-09-28 | Ambrx, Inc. | Antibody-tlr agonist conjugates, methods and uses thereof |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1992015582A1 (en) * | 1991-03-01 | 1992-09-17 | Minnesota Mining And Manufacturing Company | 1-SUBSTITUTED, 2-SUBSTITUTED 1H-IMIDAZO[4,5-c]QUINOLIN-4-AMINES |
WO1995002598A1 (en) * | 1993-07-15 | 1995-01-26 | Minnesota Mining And Manufacturing Company | Fused cycloalkylimidazopyridines |
Family Cites Families (96)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2135210A (en) * | 1937-03-13 | 1938-11-01 | John R Farrar | Golf ball |
US3314941A (en) | 1964-06-23 | 1967-04-18 | American Cyanamid Co | Novel substituted pyridodiazepins |
US3692907A (en) * | 1970-10-27 | 1972-09-19 | Richardson Merrell Inc | Treating viral infections with bis-basic ethers and thioethers of fluorenone and fluorene and pharmaceutical compositons of the same |
US3819190A (en) * | 1972-10-02 | 1974-06-25 | D Nepela | Golf ball |
US4284276A (en) * | 1980-02-13 | 1981-08-18 | Worst Joseph C | Grooved golf ball |
ZA848968B (en) | 1983-11-18 | 1986-06-25 | Riker Laboratories Inc | 1h-imidazo(4,5-c)quinolines and 1h-imidazo(4,5-c)quinolin-4-amines |
IL73534A (en) * | 1983-11-18 | 1990-12-23 | Riker Laboratories Inc | 1h-imidazo(4,5-c)quinoline-4-amines,their preparation and pharmaceutical compositions containing certain such compounds |
US4880779A (en) * | 1987-07-31 | 1989-11-14 | Research Corporation Technologies, Inc. | Method of prevention or treatment of AIDS by inhibition of human immunodeficiency virus |
US5238944A (en) | 1988-12-15 | 1993-08-24 | Riker Laboratories, Inc. | Topical formulations and transdermal delivery systems containing 1-isobutyl-1H-imidazo[4,5-c]quinolin-4-amine |
US5756747A (en) | 1989-02-27 | 1998-05-26 | Riker Laboratories, Inc. | 1H-imidazo 4,5-c!quinolin-4-amines |
US4929624A (en) | 1989-03-23 | 1990-05-29 | Minnesota Mining And Manufacturing Company | Olefinic 1H-imidazo(4,5-c)quinolin-4-amines |
US5037986A (en) | 1989-03-23 | 1991-08-06 | Minnesota Mining And Manufacturing Company | Olefinic 1H-imidazo[4,5-c]quinolin-4-amines |
NZ232740A (en) | 1989-04-20 | 1992-06-25 | Riker Laboratories Inc | Solution for parenteral administration comprising a 1h-imidazo(4,5-c) quinolin-4-amine derivative, an acid and a tonicity adjuster |
US4988815A (en) * | 1989-10-26 | 1991-01-29 | Riker Laboratories, Inc. | 3-Amino or 3-nitro quinoline compounds which are intermediates in preparing 1H-imidazo[4,5-c]quinolines |
US5054153A (en) * | 1989-12-01 | 1991-10-08 | Silliman Paul D | Golf club cleaner |
DK0553202T3 (en) * | 1990-10-05 | 1995-07-03 | Minnesota Mining & Mfg | Process for the preparation of imidazo (4,5-c) quinoline-4-amines |
US5389640A (en) | 1991-03-01 | 1995-02-14 | Minnesota Mining And Manufacturing Company | 1-substituted, 2-substituted 1H-imidazo[4,5-c]quinolin-4-amines |
US5175296A (en) * | 1991-03-01 | 1992-12-29 | Minnesota Mining And Manufacturing Company | Imidazo[4,5-c]quinolin-4-amines and processes for their preparation |
US5268376A (en) | 1991-09-04 | 1993-12-07 | Minnesota Mining And Manufacturing Company | 1-substituted 1H-imidazo[4,5-c]quinolin-4-amines |
US5266575A (en) | 1991-11-06 | 1993-11-30 | Minnesota Mining And Manufacturing Company | 2-ethyl 1H-imidazo[4,5-ciquinolin-4-amines |
IL105325A (en) | 1992-04-16 | 1996-11-14 | Minnesota Mining & Mfg | Immunogen/vaccine adjuvant composition |
FR2692159B1 (en) * | 1992-06-10 | 1996-10-11 | Vartan Berberian | BALL FOR BALL GAMES AND METHODS OF OBTAINING SUCH A BALL. |
US5395937A (en) * | 1993-01-29 | 1995-03-07 | Minnesota Mining And Manufacturing Company | Process for preparing quinoline amines |
US5648516A (en) | 1994-07-20 | 1997-07-15 | Minnesota Mining And Manufacturing Company | Fused cycloalkylimidazopyridines |
WO1995002597A1 (en) | 1993-07-15 | 1995-01-26 | Minnesota Mining And Manufacturing Company | IMIDAZO[4,5-c]PYRIDIN-4-AMINES |
US5644063A (en) | 1994-09-08 | 1997-07-01 | Minnesota Mining And Manufacturing Company | Imidazo[4,5-c]pyridin-4-amine intermediates |
US5482936A (en) | 1995-01-12 | 1996-01-09 | Minnesota Mining And Manufacturing Company | Imidazo[4,5-C]quinoline amines |
JPH09116911A (en) * | 1995-10-20 | 1997-05-02 | Canon Inc | Image pickup system |
JPH09208584A (en) | 1996-01-29 | 1997-08-12 | Terumo Corp | Amide derivative, pharmaceutical preparation containing the same, and intermediate for synthesizing the same |
JPH09255926A (en) | 1996-03-26 | 1997-09-30 | Diatex Co Ltd | Pressure-sensitive tape |
US5693811A (en) * | 1996-06-21 | 1997-12-02 | Minnesota Mining And Manufacturing Company | Process for preparing tetrahdroimidazoquinolinamines |
US5741908A (en) * | 1996-06-21 | 1998-04-21 | Minnesota Mining And Manufacturing Company | Process for reparing imidazoquinolinamines |
US5759109A (en) * | 1996-09-09 | 1998-06-02 | Martini; Byron Rocco | Simulated golf ball instructional device |
ES2290969T3 (en) * | 1996-10-25 | 2008-02-16 | Minnesota Mining And Manufacturing Company | AMENDING COMPOUNDS OF THE IMMUNE RESPONSE FOR THE TREATMENT OF DISEASES MEDIATED BY TH2 AND RELATED. |
US5939090A (en) | 1996-12-03 | 1999-08-17 | 3M Innovative Properties Company | Gel formulations for topical drug delivery |
US6069149A (en) | 1997-01-09 | 2000-05-30 | Terumo Kabushiki Kaisha | Amide derivatives and intermediates for the synthesis thereof |
UA67760C2 (en) * | 1997-12-11 | 2004-07-15 | Міннесота Майнінг Енд Мануфакчурінг Компані | Imidazonaphthyridines and use thereof to induce the biosynthesis of cytokines |
JPH11222432A (en) | 1998-02-03 | 1999-08-17 | Terumo Corp | Preparation for external use containing amide derivative inducing interferon |
JPH11255926A (en) | 1998-03-13 | 1999-09-21 | Toray Ind Inc | Silicone molding and its production |
CN1220997C (en) * | 1998-05-22 | 2005-09-28 | 松下电器产业株式会社 | Electrolytic condenser and its manufacturing method |
US6110929A (en) | 1998-07-28 | 2000-08-29 | 3M Innovative Properties Company | Oxazolo, thiazolo and selenazolo [4,5-c]-quinolin-4-amines and analogs thereof |
JP2000119271A (en) * | 1998-08-12 | 2000-04-25 | Hokuriku Seiyaku Co Ltd | 1h-imidazopyridine derivative |
US20020058674A1 (en) | 1999-01-08 | 2002-05-16 | Hedenstrom John C. | Systems and methods for treating a mucosal surface |
SK287112B6 (en) * | 1999-01-08 | 2009-12-07 | 3M Innovative Properties Company | Use of immune response modifiying compound for cervical dysplasias treatment |
US6558951B1 (en) * | 1999-02-11 | 2003-05-06 | 3M Innovative Properties Company | Maturation of dendritic cells with immune response modifying compounds |
JP2000247884A (en) | 1999-03-01 | 2000-09-12 | Sumitomo Pharmaceut Co Ltd | Arachidonic acid-induced skin disease-treating agent |
US6756382B2 (en) | 1999-06-10 | 2004-06-29 | 3M Innovative Properties Company | Amide substituted imidazoquinolines |
US6331539B1 (en) | 1999-06-10 | 2001-12-18 | 3M Innovative Properties Company | Sulfonamide and sulfamide substituted imidazoquinolines |
US6541485B1 (en) | 1999-06-10 | 2003-04-01 | 3M Innovative Properties Company | Urea substituted imidazoquinolines |
US6573273B1 (en) * | 1999-06-10 | 2003-06-03 | 3M Innovative Properties Company | Urea substituted imidazoquinolines |
US6451810B1 (en) | 1999-06-10 | 2002-09-17 | 3M Innovative Properties Company | Amide substituted imidazoquinolines |
US6376669B1 (en) * | 1999-11-05 | 2002-04-23 | 3M Innovative Properties Company | Dye labeled imidazoquinoline compounds |
US6894060B2 (en) | 2000-03-30 | 2005-05-17 | 3M Innovative Properties Company | Method for the treatment of dermal lesions caused by envenomation |
US20020055517A1 (en) * | 2000-09-15 | 2002-05-09 | 3M Innovative Properties Company | Methods for delaying recurrence of herpes virus symptoms |
JP2002145777A (en) | 2000-11-06 | 2002-05-22 | Sumitomo Pharmaceut Co Ltd | Therapeutic agent for arachidonic acid-induced dermatosis |
US6667312B2 (en) * | 2000-12-08 | 2003-12-23 | 3M Innovative Properties Company | Thioether substituted imidazoquinolines |
US6545016B1 (en) * | 2000-12-08 | 2003-04-08 | 3M Innovative Properties Company | Amide substituted imidazopyridines |
US6677347B2 (en) * | 2000-12-08 | 2004-01-13 | 3M Innovative Properties Company | Sulfonamido ether substituted imidazoquinolines |
US6660735B2 (en) * | 2000-12-08 | 2003-12-09 | 3M Innovative Properties Company | Urea substituted imidazoquinoline ethers |
US6664265B2 (en) * | 2000-12-08 | 2003-12-16 | 3M Innovative Properties Company | Amido ether substituted imidazoquinolines |
US6660747B2 (en) | 2000-12-08 | 2003-12-09 | 3M Innovative Properties Company | Amido ether substituted imidazoquinolines |
US6677348B2 (en) | 2000-12-08 | 2004-01-13 | 3M Innovative Properties Company | Aryl ether substituted imidazoquinolines |
UA74593C2 (en) | 2000-12-08 | 2006-01-16 | 3M Innovative Properties Co | Substituted imidazopyridines |
US6664260B2 (en) * | 2000-12-08 | 2003-12-16 | 3M Innovative Properties Company | Heterocyclic ether substituted imidazoquinolines |
UA74852C2 (en) | 2000-12-08 | 2006-02-15 | 3M Innovative Properties Co | Urea-substituted imidazoquinoline ethers |
US6545017B1 (en) * | 2000-12-08 | 2003-04-08 | 3M Innovative Properties Company | Urea substituted imidazopyridines |
US20020110840A1 (en) | 2000-12-08 | 2002-08-15 | 3M Innovative Properties Company | Screening method for identifying compounds that selectively induce interferon alpha |
US6664264B2 (en) * | 2000-12-08 | 2003-12-16 | 3M Innovative Properties Company | Thioether substituted imidazoquinolines |
US6525064B1 (en) | 2000-12-08 | 2003-02-25 | 3M Innovative Properties Company | Sulfonamido substituted imidazopyridines |
WO2002102377A1 (en) | 2001-06-15 | 2002-12-27 | 3M Innovative Properties Company | Immune response modifiers for the treatment of periodontal disease |
MXPA04001972A (en) | 2001-08-30 | 2005-02-17 | 3M Innovative Properties Co | Methods of maturing plasmacytoid dendritic cells using immune response modifier molecules. |
EP1478371A4 (en) | 2001-10-12 | 2007-11-07 | Univ Iowa Res Found | Methods and products for enhancing immune responses using imidazoquinoline compounds |
WO2003043572A2 (en) | 2001-11-16 | 2003-05-30 | 3M Innovative Properties Company | Methods and compositions related to irm compounds and toll-like receptor pathways |
AU2004220469B2 (en) | 2001-11-29 | 2010-07-29 | 3M Innovative Properties Company | Methods of improving skin quality |
RU2327460C2 (en) | 2001-11-29 | 2008-06-27 | 3М Инновейтив Пропертиз Компани | Immunomodulator-containing pharmaceutical formulations |
US6677349B1 (en) | 2001-12-21 | 2004-01-13 | 3M Innovative Properties Company | Sulfonamide and sulfamide substituted imidazoquinolines |
MXPA04008023A (en) | 2002-02-22 | 2004-11-26 | 3M Innovative Properties Co | Method of reducing and treating uvb-induced immunosuppression. |
GB0211649D0 (en) | 2002-05-21 | 2002-07-03 | Novartis Ag | Organic compounds |
AU2003233519A1 (en) | 2002-05-29 | 2003-12-19 | 3M Innovative Properties Company | Process for imidazo(4,5-c)pyridin-4-amines |
CA2488801A1 (en) | 2002-06-07 | 2003-12-18 | 3M Innovative Properties Company | Ether substituted imidazopyridines |
DE60335010D1 (en) | 2002-08-15 | 2010-12-30 | 3M Innovative Properties Co | IMMUNOSTIMULATORY COMPOSITIONS AND METHOD FOR STIMULATING AN IMMUNE RESPONSE |
JP2006503068A (en) | 2002-09-26 | 2006-01-26 | スリーエム イノベイティブ プロパティズ カンパニー | 1H-Imidazo dimer |
AU2003287316A1 (en) | 2002-12-11 | 2004-06-30 | 3M Innovative Properties Company | Assays relating to toll-like receptor activity |
WO2004053057A2 (en) | 2002-12-11 | 2004-06-24 | 3M Innovative Properties Company | Gene expression systems and recombinant cell lines |
AU2003301052A1 (en) * | 2002-12-20 | 2004-07-22 | 3M Innovative Properties Company | Aryl / hetaryl substituted imidazoquinolines |
JP2006512391A (en) | 2002-12-30 | 2006-04-13 | スリーエム イノベイティブ プロパティズ カンパニー | Combination immunostimulant |
JP2006517974A (en) | 2003-02-13 | 2006-08-03 | スリーエム イノベイティブ プロパティズ カンパニー | Methods and compositions for IRM compounds and Toll-like receptor 8 |
EP1599726A4 (en) | 2003-02-27 | 2009-07-22 | 3M Innovative Properties Co | Selective modulation of tlr-mediated biological activity |
JP2006519866A (en) | 2003-03-04 | 2006-08-31 | スリーエム イノベイティブ プロパティズ カンパニー | Prophylactic treatment of UV-induced epidermal neoplasia |
US20040176367A1 (en) | 2003-03-07 | 2004-09-09 | 3M Innovative Properties Company | 1-Amino 1H-imidazoquinolines |
AU2004220465A1 (en) | 2003-03-13 | 2004-09-23 | 3M Innovative Properties Company | Method of tattoo removal |
CA2518082C (en) | 2003-03-13 | 2013-02-12 | 3M Innovative Properties Company | Methods for diagnosing skin lesions |
EP1613956A2 (en) | 2003-03-25 | 2006-01-11 | 3M Innovative Properties Company | Selective activation of cellular activities mediated through a common toll-like receptor |
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OA13310A (en) | 2003-09-05 | 2007-04-13 | Anadys Pharmaceuticals Inc | TLR7 ligands for the treatment of hepatitis C. |
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2003
- 2003-05-28 NO NO20032452A patent/NO20032452L/en not_active Application Discontinuation
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- 2003-10-29 US US10/696,476 patent/US20040092545A1/en not_active Abandoned
-
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- 2004-09-20 HK HK04107230A patent/HK1064383A1/en not_active IP Right Cessation
- 2004-11-11 HK HK04108904A patent/HK1066005A1/en not_active IP Right Cessation
-
2005
- 2005-01-25 HK HK05100647A patent/HK1069166A1/en not_active IP Right Cessation
- 2005-02-28 US US11/069,033 patent/US7132429B2/en not_active Expired - Fee Related
- 2005-05-19 US US11/132,900 patent/US7612083B2/en not_active Expired - Fee Related
- 2005-08-24 CY CY20051101024T patent/CY1105586T1/en unknown
-
2007
- 2007-05-09 CY CY20071100621T patent/CY1106569T1/en unknown
-
2009
- 2009-11-06 JP JP2009255040A patent/JP2010031040A/en not_active Ceased
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1992015582A1 (en) * | 1991-03-01 | 1992-09-17 | Minnesota Mining And Manufacturing Company | 1-SUBSTITUTED, 2-SUBSTITUTED 1H-IMIDAZO[4,5-c]QUINOLIN-4-AMINES |
WO1995002598A1 (en) * | 1993-07-15 | 1995-01-26 | Minnesota Mining And Manufacturing Company | Fused cycloalkylimidazopyridines |
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