Treatment of asthma with MEK inhibitors

Abstract

This invention provides a method of preventing or treating asthma by administering to a patient in need of treatment an effective amount of a selective MEK inhibitor, especially a phenyl amine of Formula I and II: 1

Description

FIELD OF THE INVENTION

[0002] This invention relates to a method for preventing and treating asthma in mammals comprising administering a compound characterized as an inhibitor of a family of enzymes known as MEK kinases, which are groups of MAP (mitogen-associated protein kinase) and Erk (extracellular signal-regulated) Kinases. These are enzymes that regulate phosphorylation of substrates in mammals.

BACKGROUND OF THE INVENTION

[0003] Asthma is a heterogeneous disorder of the airways that afflicts millions of people. Airway inflammation, hyperresponsiveness, and obstruction characterize the condition. The disease often causes spasms of the bronchial smooth muscle system, and affects both the upper and lower respiratory tracts. There are several forms of asthma, characterized by varying degrees of severity. Mild asthma, for example, is defined as brief episodes of wheezing, with or without dyspnea or cough. Moderately severe asthma is defined as wheezing and dyspnea, and can be with or without cough and expectoration, but generally interferes with daily activities and/or sleeping. Severe asthma is characterized by incapacitation due to dyspnea, and the afflicted patient typically is unable to eat or sleep normally, is very anxious, and is often exhausted. A condition known as status asthmaticus is the most severe form of asthma, and generally requires intensive hospital care, and may even prove fatal. The disease may occur as a result of both allergic and nonallergic mechanisms.

[0004] While there are several treatments available for relieving the symptoms and discomfort associated with asthma, there are no cures. Moreover, the current treatments often cause side effects that exacerbate the discomfort and precipitate other debilitating conditions. Mild asthma generally is treated with beta-adrenergic drugs, as well as antihistamines, especially in the case of children, to prevent or abort sporadic episodes. Moderately severe and severe asthma are generally treated with adrenergic agents and bronchodilators, as well as corticosteroids. Other actions caused by antiasthmatic agents which limit their widespread use include headache, fatigue, dry mouth, nervousness, and in some cases addiction and substance abuse. Recent advances in the understanding of the pathogenesis and treatment of asthma is discussed more fully by Grayson et al., The Mount Sinai Journal of Medicine, September 1998;65(4):246-256.

[0005] Because asthma is so prevalent in both children and adults, there is an on-going need for agents that can treat the disease, or at least relieve the symptoms that accompany the disease, without causing undesirable side effects. We have now discovered that MEK inhibitors are particularly useful for treating asthma and relieving the symptoms that accompany the disease. An object of this invention is therefore to provide a new method for preventing and treating asthmatic conditions.

SUMMARY OF THE INVENTION

[0006] This invention provides a method of preventing and treating asthma, said method comprising the step of administering to a patient an antiasthmatic-effective amount of a MEK inhibitor. Selective MEK inhibitors are those compounds which inhibit the MEK 1 and MEK 2 enzymes without substantial inhibition of other such enzymes. In a preferred embodiment, the invention provides a method for preventing or treating asthma by administering a MEK inhibitor. In a further embodiment, the invention provides a method for preventing and/or treating asthma comprising administering an effective amount of the selective MEK inhibitor described in U.S. Pat. No. 5,525,625, incorporated herein by reference, which selective MEK inhibitor is 2-(2-amino-3-methoxyphenyl)-4-oxo-4H-[1]benzopyran.

[0007] In another preferred embodiment, the MEK inhibitor to be administered is a phenyl amine derivative of Formula I: 2

[0008] In Formula (I), R1 is hydrogen, hydroxy, C1-C8 alkyl, C1-C8 alkoxy, halo, trifluoromethyl, or CN. R2 is hydrogen. R3, R4, and R5 are independently selected from hydrogen, hydroxy, halo, trifluoromethyl, C1-C8 alkyl, C1-C8 alkoxy, nitro, CN, and —(O or NH)m—(CH2)n—R9. R9 is hydrogen, hydroxy, COOH, or NR10R11; n is 0-4; m is 0 or 1. Each of R10 and R11 is independently selected from hydrogen and C1-C8 alkyl, or taken together with the nitrogen to which they are attached can complete a 3-10 member cyclic ring optionally containing 1, 2, or 3 additional heteroatoms selected from O, S, NH, or N—(C1-C8 alkyl). Z is COOR7, tetrazolyl, CONR6R7, CONHNR10R11, or CH2OR7. R6 and R7 independently are hydrogen, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, (CO)—C1-C8 alkyl, aryl, heteroaryl, C3-C10 cycloalkyl, or C3-C10 (cycloalkyl optionally containing one, two, or three heteroatoms selected from O, S, NH, or N alkyl); or R6 and R7 together with the nitrogen to which they are attached complete a 3-10 member cyclic ring optionally containing 1, 2, or 3 additional heteroatoms selected from O, S, NH, or N alkyl. In formula (I), any of the foregoing alkyl, alkenyl, aryl, heteroaryl, heterocyclic, and alkynyl groups can be unsubstituted or substituted by halo, hydroxy, C1-C6 alkoxy, amino, nitro, C1-C4 alkylamino, di(C1-C4)alkylamino, C3-C6 cycloalkyl, phenyl, phenoxy, C3-C5 heteroaryl or heterocyclic radical, or C3-C5 heteroaryloxy or heterocyclic radical-oxy. The invention also provides a pharmaceutically acceptable salt, ester, amide, or prodrug of each of the disclosed MEK inhibitors.

[0009] Preferred embodiments of Formula (I) have a structure wherein: (a) R1 is hydrogen, methyl, methoxy, fluoro, chloro, or bromo; (b) R2 is hydrogen; (c) R3, R4, and R5 independently are hydrogen, fluoro, chloro, bromo, iodo, methyl, methoxy, or nitro; (d) R10 and R11 independently are hydrogen or methyl; (e) Z is COOR7, tetrazolyl, CONR6R7, CONHNR10R11, or CH2OR7; R6 and R7 independently are hydrogen, C1-4 alkyl, heteroaryl, or C3-5 cycloalkyl optionally containing one or two heteroatoms selected from O, S, or NH; or R6 and R7 together with the nitrogen to which they are attached complete a 5-6 member cyclic ring optionally containing 1 or 2 additional heteroatoms selected from O, NH or N-alkyl; and wherein any of the foregoing alkyl or aryl groups can be unsubstituted or substituted by halo, hydroxy, methoxy, ethoxy, or heteroaryloxy (such as 2,3,4,5,6-pentafluorophenyl); (f) Z is COOR7; (g) R7 is H, pentafluorophenyl, or tetrazolyl; (h) R3, R4, and R5 are independently H, fluoro, or chloro; (i) R4 is fluoro; (j) two of R3, R4, and R5 are fluoro; or (k) or combinations of the above. In another preferred embodiment of Formula (I), R1 is methyl, fluoro, chloro, or bromo.

[0010] In a more preferred embodiment, the MEK inhibitor is selected from a compound in Formula (I) Compound Table below.

Formula (I) Compound Table (Page 1 of 10)

[0011] [4-Chloro-2-(1H-tetrazol-5-yl)-phenyl-(4-iodo-2-methyl-phenyl)-amine

[0012] (4-iodo-2-methyl-phenyl)-[2-(1H-tetrazol-5-yl)-phenyl]amine

[0013] [4-nitro-2-(1H-tetrazol-5-yl)-phenyl-(4-iodo-2-methyl-phenyl)-amine

[0014] 4-Fluoro-2-(4-iodo-2-methylphenylamino)benzoic acid

[0015] 3,4,5-Trifluoro-2-(4-iodo-2-methyl-phenylamino)-benzoic acid

[0016] 3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-benzoic acid

[0017] 5-Bromo-3,4-difluoro-2-(4-iodo-2-methyl-phenylamino)-benzoic acid

[0018] 5-Chloro-2-(4-iodo-2-methyl-phenylamino)-benzoic acid

[0019] Sodium 5-Chloro-2-(4-iodo-2-methyl-phenylamino)-benzoate

[0020] 5-Bromo-2-(4-iodo-2-methyl-phenylamino)-benzoic acid

[0021] 2-(4-Iodo-2-methyl-phenylamino)-5-nitro-benzoic acid

[0022] 4-Chloro-2-(4-iodo-2-methyl-phenylamino)-benzoic acid

[0023] 2-(4-Iodo-2-methyl-phenylamino)-benzoic acid

[0024] 5-Fluoro-2-(4-iodo-2-methyl-phenylamino)-benzoic acid

[0025] 5-Iodo-2-(4-iodo-2-methyl-phenylamino)-benzoic acid

[0026] 2,3,5-Trifluoro-4-(4-iodo-2-methyl-phenylamino)-benzoic acid

[0027] 2-(4-Iodo-phenylamino)-5-methoxy-benzoic acid

[0028] 5-Methyl-2-(4-iodo-2-methyl-phenylamino)-benzoic acid

[0029] 2-(4-Iodo-2-methyl-phenylamino)-4-nitro-benzoic acid

[0030] 2-(4-Bromo-2-methyl-phenylamino)-4-fluoro-benzoic acid

[0031] 2-(2-Bromo-4-iodo-phenylamino)-5-nitro-benzoic acid

[0032] 2-(4-Bromo-2-methyl-phenylamino)-3,4-difluoro-benzoic acid

[0033] 5-Chloro-N-(2-hydroxyethyl)-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0034] 4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0035] 4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-methyl-benzamide

[0036] N-Ethyl-4-fluoro-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0037] 4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N,N-dimethyl-benzamide

[0038] 4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-(1H-tetrazol-5-yl)-benzamide

Formula (I) Compound Table (Continued, Page 2 of 10)

[0039] 5-Bromo-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0040] 5-Chloro-2-(4-iodo-2-methyl-phenylamino)-N,N-dimethyl-benzamide

[0041] [5-Chloro-2-(4-iodo-2-methyl-phenylamino)-benzoylamino]-acetic acid

[0042] 4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-propyl-benzamide

[0043] 5-Bromo-N-(2-hydroxy-ethyl)-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0044] N,N-Diethyl-4-fluoro-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0045] 4-Fluoro-N-{3-[4-(2-hydroxy-ethyl)-piperazin-1-yl]-propyl}-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0046] N,N-Diethyl-2-(4-iodo-2-methyl-phenylamino)-5-nitro-benzamide

[0047] N-Butyl-4-fluoro-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0048] 5-Chloro-N,N-diethyl-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0049] 5-Bromo-2-(4-iodo-2-methyl-phenylamino)-N,N-dimethyl-benzamide

[0050] 5-Bromo-3,4-difluoro-N-(2-hydroxy-ethyl)-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0051] N-(2,3-Dihydroxy-propyl)-3,4-difluoro-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0052] 5-Bromo-3,4-difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(2-piperidin-1-yl-ethyl)-benzamide

[0053] 3,4-Difluoro-N-(2-hydroxy-ethyl)-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0054] N-(2,3-Dihydroxy-propyl)4-fluoro-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0055] 3,4-Difluoro-N-(3-hydroxy-propyl)-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0056] 5-Bromo-3,4-difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(2-pyrrolidin-1-yl-ethyl)-benzamide

[0057] 5-Bromo-3,4-difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(2-pyridin4-yl-ethyl)-benzamide

Formula (I) Compound Table (Continued, Page 3 of 10)

[0058] 4-Fluoro-N-(2-hydroxy-ethyl)-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0059] 5-Bromo-N-(3-dimethylamino-propyl)-3,4-difluoro-2-(4-iodo-2-methylphenylamino)-benzamide

[0060] 5-Bromo-3,4-difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(2-morpholin-4-yl-ethyl)-benzamide

[0061] 3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(2-morpholin-4-yl-ethyl)-benzamide

[0062] 3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(2-pyrrolidin-1-yl-ethyl)-benzamide

[0063] 3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(2-pyridin-4-yl-ethyl)-benzamide

[0064] N-(3-Dimethylamino-propyl)-3,4-difluoro-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0065] N-Benzyl-4-fluoro-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0066] 2-(4-Bromo-2-methyl-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethyl)-benzamide

[0067] 4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-(2-morpholin-4-yl-ethyl)-benzamide

[0068] 4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-(3-piperidin-1-yl-propyl)-benzamide

[0069] 3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(3-piperidin-1-yl-propyl)-benzamide

[0070] 4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-(2-thiophen-2-yl-ethyl)-benzamide

[0071] 4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-(2-pyrrolidin-1-yl-ethyl)-benzamide

[0072] 2-(4-Bromo-2-methyl-phenylamino)-3,4-difluoro-N-(2-morpholin4-yl-ethyl)-benzamide

Formula (I) Compound Table (Continued, Page 4 of 10)

[0073] 5-Bromo-3,4-difluoro-2-(4-iodo-2-methyl-phenylamino)-N-pyridin-4-ylmethyl-benzamide

[0074] 3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-N-pyridin-4-ylmethyl-benzamide

[0075] 2-(4-Bromo-2-methyl-phenylamino)-N-(3-dimethylamino-propyl)-3,4-difluoro-benzamide

[0076] 4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-pyridin-4-ylmethyl-enzamide

[0077] 4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-(2-pyridin-4-yl-ethyl)-benzamide

[0078] 2-(4-Bromo-2-methyl-phenylamino)-3,4-difluoro-N-(2-pyridin-4-yl-ethyl)-benzamide

[0079] 2-(4-Bromo-2-methyl-phenylamino)-3,4-difluoro-N-(3-hydroxy-propyl)-benzamide

[0080] 2-(4-Bromo-2-methyl-phenylamino)-3,4-difluoro-N-(2-pyrrolidin-1-yl-ethyl)-benzamide

[0081] 4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-phenethyl-benzamide

[0082] 2-(4-Bromo-2-methyl-phenylamino)-3,4-difluoro-N-(2-thiophen-2-yl-ethyl)-benzamide

[0083] 2-(4-Bromo-2-methyl-phenylamino)-3,4-difluoro-N-pyridin-4-ylmethyl-benzamide

[0084] 2-(4-Bromo-2-methyl-phenylamino)-3,4-difluoro-N-phenethyl-benzamide

[0085] 2-(4-Bromo-2-methyl-phenylamino)-3,4-difluoro-N-(2-piperidin-1-yl-ethyl)-benzamide

[0086] 5-Chloro-N-{3-[4-(2-hydroxy-ethyl)-piperazin-1-yl]-propyl}-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0087] 5-Fluoro-N-{3-[4-(2-hydroxy-ethyl)-piperazin-1-yl]-propyl}-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0088] 2-(4-Iodo-2-methyl-phenylamino)-5-nitro-N-pyridin-4-yl methyl-benzamide

Formula (I) Compound Table (Continued, Page 5 of 10)

[0089] 5-Bromo-N-{3-[4-(2-hydroxy-ethyl)-piperazin-1-yl -propyl}-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0090] 5-Chloro-N-(2-diethylamino-ethyl)-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0091] 5-Chloro-2-(4-iodo-2-methyl-phenylamino)-N-(2-piperidin-1-yl-ethyl)-benzamide

[0092] (3-Hydroxy-pyrrolidin-1-yl)-[5-nitro-2-(4-iodo-2-methyl-phenylamino)-phenyl}-methanone

[0093] 5-Chloro-2-(4-iodo-2-methyl-phenylamino)-N-(2-pyrrolidin-1-yl-ethyl)-benzamide

[0094] 5-Bromo-N-(2-diethylamino-ethyl)-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0095] N-{2-[Bis-(2-hydroxy-ethyl)-amino]-ethyl}-5-chloro-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0096] N-{2-[Bis-(2-hydroxy-ethyl)-amino]-ethyl}-5-bromo-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0097] N-{3-[4-(2-Hydroxy-ethyl)-piperazin-1-yl]-propyl}-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0098] 5-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-pyridin-4-ylmethyl-benzamide

[0099] 5-Bromo-2-(4-iodo-2-ethyl-phenylamino)-N-(2-pyrrolidin-1-yl-ethyl)-benzamide

[0100] 5-Bromo-2-(4-iodo-2-methyl-phenylamino)-N-(2-piperidin-1-yl-ethyl)-benzamide

[0101] 5-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-(2-pyrrolidin-1-yl-ethyl)-benzamide

[0102] 5-Chloro-N-(3-dimethylamino-propyl)-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0103] N-{2-[Bis-(2-hydroxy-ethyl)-amino]-ethyl}-5-fluoro-2-(4-iodo-2-methyl-phenylamino)-benzamide

Formula (I) Compound Table (Continued, Page 6 of 10)

[0104] 5-Chloro-N-(3-hydroxy-propyl)-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0105] 5-Chloro-N-(3-diethylamino-2-hydroxy-propyl)-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0106] 5-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-(2-piperidin-1-yl-ethyl)-benzamide

[0107] 5-Bromo-N-(3-hydroxy-propyl)-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0108] 5-Bromo-2-(4-iodo-2-methyl-phenylamino)-N-(3-piperidin-1-yl-propyl)-benzamide

[0109] N-{2-[Bis-(2-hydroxy-ethyl)-amino]-ethyl}-2-(4-iodo-2-methyl-phenylamino)-5-nitro-benzamide

[0110] 5-Chloro-2-(4-iodo-2-methyl-phenylamino)-N-(2-morpholin-4-yl-ethyl)-benzamide

[0111] 5-Chloro-N-(3-diethylamino-propyl)-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0112] 5-Chloro-N-(2-diisopropylamino-ethyl)-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0113] 5-Chloro-2-(4-iodo-2-methyl-phenylamino)-N-(3-piperidin-1-yl-propyl)-benzamide

[0114] 2-(4-Iodo-2-methyl-phenylamino)-5-nitro-N-(2-piperidin-1-yl-ethyl)-benzamide

[0115] 5-Bromo-2-(4-iodo-2-methyl-phenylamino)-N-(2-piperazin-1-yl-ethyl)-benzamide

[0116] N-(2-Diethylamino-ethyl)-5-fluoro-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0117] 5-Bromo-N-(3-dimethylamino-propyl)-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0118] N-(3-Hydroxy-propyl)-2-(4-iodo-2-methyl-phenylamino)-5-nitro-benzamide

Formula (I) Compound Table (Continued, Page 7 of 10)

[0119] 5-Fluoro-N-(3-hydroxy-propyl)-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0120] N-(3-Diethylamino-propyl)-5-fluoro-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0121] N-(3-Diethylamino-propyl)-2-(4-iodo-2-methyl-phenylamino)-5-nitro-benzamide

[0122] 5-Bromo-2-(4-iodo-2-methyl-phenylamino)-N-(2-morpholin-4-yl-ethyl)-benzamide

[0123] 2-(4-Iodo-2-methyl-phenylamino)-5-nitro-N-(3-piperidin-1-yl-propyl)-benzamide

[0124] [5-Fluoro-2-(4-iodo-2-methyl-phenylamino)-phenyl]-(2 or 3-hydroxy-pyrrolidin-1-yl)-methanone

[0125] 5-Bromo-N-(2-diisopropylamino-ethyl)-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0126] 5-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-(2-morpholin-4-yl-ethyl)-benzamide

[0127] 5-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-(3-piperidin-1-yl-propyl)-benzamide

[0128] [5-Fluoro-2-(4-iodo-2-methyl-phenylamino)-phenyl]-4-(2-hydroxy-ethyl)-piperazin-1-yl)-methanone

[0129] N-(3-Diethylamino-2-hydroxy-propyl)-5-fluoro-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0130] N-Cyclopropyl-5-fluoro-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0131] 5-Chloro-N-(2-hydroxy-ethyl)-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0132] 5-Fluoro-N-(2-hydroxy-ethyl)-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0133] N-Benzyloxy-5-fluoro-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0134] N-Benzyloxy-5-bromo-2-(4-iodo-2-methyl-phenylamino)-benzamide

Formula (I) Compound Table (Continued, Page 8 of 10)

[0135] 2-(4-Iodo-2-methyl-phenylamino)-5-nitro-N-(4-sulfamoyl-benzyl)-benzamide

[0136] 5-Bromo-N-(2-hydroxy-ethyl)-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0137] N-(2-Hydroxy-ethyl)-5-iodo-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0138] N-(2-Hydroxy-ethyl)-2-(4-iodo-2-ethyl-phenylamino)-5-nitro-benzamide

[0139] 2-(4-Iodo-2-methyl-phenylamino)-N-methyl-5-nitro-N-phenyl-benzamide

[0140] 5-Chloro-N-cyclopropyl-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0141] 5-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-methyl-N-phenyl-benzamide

[0142] N-Allyl-5-fluoro-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0143] N-Benzyloxy-5-iodo-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0144] 5-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-(4-sulfamoyl-benzyl)-benzamide

[0145] N-Allyl-5-chloro-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0146] N-Cyclopropyl-2-(4-iodo-2-methyl-phenylamino)-5-nitro-benzamide

[0147] 5-Bromo-N-cyclopropyl-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0148] 5-Chloro-2-(4-iodo-2-methyl-phenylamino)-N-methyl-N-phenyl-benzamide

[0149] 5-Iodo-2-(4-iodo-2-methyl-phenylamino)-N-(4-sulfamoyl-benzyl)-benzamide

[0150] 5-Bromo-2-(4-iodo-2-methyl-phenylamino)-N-(4-sulfamoyl-benzyl)-benzamide

[0151] N-Allyl-2-(4-iodo-2-methyl-phenylamino)-5-nitro-benzamide

[0152] 2-(4-Iodo-2-methyl-phenylamino)-5-nitro-N-(4-sulfamoyl-benzyl)-benzamide

[0153] N-Allyl-5-bromo-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0154] 5-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-(3-methyl-benzyl)-benzamide

[0155] N-Cyclopropyl-5-iodo-2-(4-iodo-2-methyl-phenylamino)-benzamide

Formula (I) Compound Table (Continued, Page 9 of 10)

[0156] 5-Bromo-2-(4-iodo-2-methyl-phenylamino)-N-methyl-N-phenyl-benzamide

[0157] N-Benzyloxy-2-(4-iodo-2-methyl-phenylamino)-5-nitro-benzamide

[0158] N-Cyclohexyl-5-iodo-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0159] N-Allyl-5-iodo-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0160] 5-Iodo-2-(4-iodo-2-methyl-phenylamino)-N-(3-methyl-benzyl)-benzamide

[0161] 2-(4-Iodo-2-methyl-phenylamino)-N-(3-methyl-benzyl)-5-nitro-benzamide

[0162] 5-Iodo-2-(4-iodo-2-methyl-phenylamino)-N-methyl-N-phenyl-benzamide

[0163] N-Cyclohexyl-5-fluoro-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0164] 5-Chloro-N-cyclohexyl-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0165] 5-Bromo-2-(4-iodo-2-methyl-phenylamino)-N-(3-methyl-benzyl)-benzamide

[0166] 5-Bromo-N-cyclohexyl-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0167] 5-Chloro-2-(4-iodo-2-methyl-phenylamino)-N-(3-methyl-benzyl)-benzamide

[0168] N-Cyclohexyl-2-(4-iodo-2-methyl-phenylamino)-5-nitro-benzamide

[0169] N-Benzyloxy-5-bromo-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0170] N-Benzyloxy-5-fluoro-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0171] 5-Chloro-N-(2-hydroxy-ethyl)-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0172] 5-Bromo-N-(2-hydroxy-ethyl)-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0173] 2-(4-Iodo-2-methyl-phenylamino)-N-methyl-5-nitro-N-phenyl-benzamide

[0174] 5-Chloro-2-(4-iodo-2-methyl-phenylamino)-N-methyl-N-phenyl-benzamide

[0175] N-(2-Hydroxy-ethyl)-5-iodo-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0176] 5-Chloro-N-cyclopropyl-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0177] N-Allyl-5-chloro-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0178] 5-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-methyl-N-phenyl-benzamide

Formula (I) Compound Table (Continued, Page 10 of 10)

[0179] N-(2-Hydroxy-ethyl)-2-(4-iodo-2-methyl-phenylamino)-5-nitro-benzamide

[0180] 5-Fluoro-N-(2-hydroxy-ethyl)-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0181] 5-Bromo-N-cyclopropyl-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0182] N-Cyclopropyl-5-fluoro-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0183] 5-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-(4-sulfamoyl-benzyl)-benzamide

[0184] N-Cyclopropyl-2-(4-iodo-2-methyl-phenylamino)-5-nitro-benzamide

[0185] N-Allyl-5-fluoro-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0186] N-Benzyloxy-5-iodo-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0187] N-Allyl-5-bromo-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0188] 5-Bromo-2-(4-iodo-2-methyl-phenylamino)-N-(4-sulfamoyl-benzyl)-benzamide

[0189] N-Allyl-2-(4-iodo-2-methyl-phenylamino)-5-nitro-benzamide

[0190] 4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-benzyl alcohol

[0191] [5-Chloro-2-(4-iodo-2-methyl-phenylamino)-phenyl]-methanol

[0192] [2-(4-Iodo-2-methyl-phenylamino)-5-nitro-phenyl]-methanol

[0193] [5-Bromo-2-(4-iodo-2-methyl-phenylamino)-phenyl]-methanol

[0194] N-Allyl-2-(4-iodo-2-methyl-phenylamino)-5-nitro-benzamide.

[0195] In another preferred embodiment, the MEK inhibitor is a compound of Formula II 3

[0196] In Formula (II), R1a is hydrogen, hydroxy, C1-C8 alkyl, C1-C8 alkoxy, halo, trifluoromethyl, or CN. R2a is hydrogen. Each of R3a, R4a, and R5a is independently selected from hydrogen, hydroxy, halo, trifluoromethyl, C1-C8 alkyl, C1-C8 alkoxy, nitro, CN, and (O or NH)m—(CH2)n—R9a. R9a is hydrogen, hydroxy, CO2H or NR10aR11a; n is 0-4; and m is 0 or 1. Each of R10a and R11a is independently hydrogen or C1-C8 alkyl, or taken together with the nitrogen to which they are attached can complete a 3- to 10-member cyclic ring optionally containing one, two, or three additional heteroatoms selected from O, S, NH, or N—(C1-C8 alkyl). R6a is hydrogen, C1-C8 alkyl, (CO)—(C1-C8 alkyl), aryl, aralkyl, or C3-C10 cycloalkyl. R7a is hydrogen, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, C3-C10 (cycloalkyl or cycloalkyl optionally containing a heteroatom selected from O, S, or NR9a). In Formula (II), any of the foregoingany of the foregoing alkyl, alkenyl, aryl, heteroaryl, heterocyclic, and alkynyl groups can be unsubstituted or substituted by halo, hydroxy, C1-C6 alkoxy, amino, nitro, C1-C4 alkylamino, di(C1-C4)alkylamino, C3-C6 cycloalkyl, phenyl, phenoxy, C3-C5 heteroaryl or heterocyclic radical, or C3-C5 heteroaryloxy or heterocyclic radical-oxy; or R6a and R7a taken together with the N to which they are attached can complete a 5- to 10-membered cyclic ring, optionally containing one, two, or three additional heteroatoms selected from O, S, or NR10aR11a. The invention also encompasses pharmaceutically acceptable salts, esters, amides or prodrugs of each of the disclosed compounds.

[0197] Preferred embodiments of Formula (II) are those structures wherein: (a) R1a is H, methyl, fluoro, or chloro; (b) R2a is H; R3a, R4a and R5a are each H, Cl, nitro, or F; (c) R6a is H; (d) R7a is methyl, ethyl, 2-propenyl, propyl, butyl, pentyl, hexyl, cyclopropylmethyl, cyclobutyl methyl, cyclopropylmethyl, or cyclopropylethyl; (e) the 4′ position is I, rather than Br; (f) R4a is F at the 4 position, para to the CO—N—R6a—OR7a group and meta to the bridging nitrogen; (f) R3a or R5a is F; (g) at least one of R3a, R4a and R5a is F; (h) R1a is methyl or chloro; or (i) or a combination of the above.

[0198] In a more preferred embodiment the MEK inhibitor is a compound selected from Formula (II) Compound Table below.

Formula (II) Compound Table (Page 1 of 7)

[0199] 4-Fluoro-N-hydroxy-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0200] 4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-(methoxy)-benzamide

[0201] 4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-(prop-2-ynyloxy)-benzamide

[0202] 4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-(2-phenoxyethoxy)-benzamide

[0203] 4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-(2-thienylmethoxy)-benzamide

[0204] 4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-(prop-2-enyloxy)-benzamide

[0205] 4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-(cyclopropylmethoxy)-benzamide

[0206] 4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-(cyclopentoxy)-benzamide

[0207] 3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(3-furylmethoxy)-benzamide

[0208] 3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-N-ethoxy-benzamide

[0209] 3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(but-2-enyloxy)-benzamide

[0210] 3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(cyclopropylmethoxy)-benzamide

[0211] 3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(1-methylprop-2-ynyloxy)-benzamide

[0212] 3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(3-phenylprop-2-ynyloxy)-benzamide

[0213] 3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(3-methyl-5-phenylpent-2-en-4-ynyloxy)-benzamide

[0214] 3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(prop-2-ynyloxy)-benzamide

[0215] 3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(propoxy)-benzamide

Formula (II) Compound Table (Continued, Page 2 of 7)

[0216] 3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(cyclobutyloxy)-benzamide

[0217] 3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(2-thienylmethoxy)-benzamide

[0218] 3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(2-methyl-prop-2-enyloxy)-benzamide

[0219] 3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(2-phenoxyethoxy)-benzamide

[0220] 3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(but-2-enyloxy)-benzamide

[0221] 3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(but-3-ynyloxy)-benzamide

[0222] 3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(cyclopentyloxy)-benzamide

[0223] 3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(3-(2-fluorophenyl)-prop-2-ynyloxy)-benzamide

[0224] 5-Bromo-3,4-difluoro-N-hydroxy-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0225] 5-Bromo-3,4-difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(n-propoxy)-benzamide

[0226] 5-Bromo-3,4-difluoro-N-(furan-3-ylmethoxy)-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0227] 5-Bromo-N-(but-2-enyloxy)-3,4-difluoro-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0228] 5-Bromo-N-butoxy-3,4-difluoro-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0229] 5-Bromo-3,4-difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(3-methyl-but-2-enyloxy)-benzamide

[0230] 5-Bromo-3,4-difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(3-methyl-pent-2-en-4-ynyloxy)-benzamide

Formula (II) Compound Table (Continued, Page 3 of 7)

[0231] 5-Bromo-3,4-difluoro-2-(4-iodo-2-methyl-benzyl)-N-[5-(3-methoxy-phenyl)-3-methyl-pent-2-en-4-ynyloxy]-benzamide

[0232] 5-Bromo-3,4-difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(prop-2-ynyloxy)-benzamide

[0233] 5-Bromo-3,4-difluoro-2-(4-iodo-2-methyl-phenylamino)-N-[3-(3-methoxy-phenyl)-prop-2-ynyloxy]-benzamide

[0234] 5-Bromo-3,4-difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(thiopen-2-ylmethoxy)-benzamide

[0235] 5-Bromo-3,4-difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(pyridin-3-ylmethoxy)-benzamide

[0236] 5-Bromo-3-4-difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(3-(2-fluorophenyl)-prop-2-ynyloxy)-benzamide

[0237] 5-Bromo-3,4-difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(ethoxy)-benzamide

[0238] 5-Bromo-3,4-difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(cyclopropylmethoxy)-benzamide

[0239] 5-Bromo-3,4-difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(isopropoxy)-benzamide

[0240] 5-Bromo-3,4-difluoro-2-(4-iodo-2-methyl-phenylamino)-N-but-3-ynyloxy)-benzamide

[0241] 5-Chloro-N-hydroxy-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0242] 5-Chloro-2-(4-iodo-2-methyl-phenylamino)-N-(tetrahydro-pyran-2-yloxy)-benzamide

[0243] 5-Chloro-2-(4-iodo-2-methyl-phenylamino)-N-methoxy-benzamide

[0244] 4-Bromo-2-(4-iodo-2-methyl-phenylamino)-N-phenylmethoxy-benzamide

[0245] 4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-phenylmethoxy-benzamide

[0246] 5-Fluoro-N-hydroxy-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0247] 5-Iodo-2-(4-iodo-2-methyl-phenylamino)-N-phenylmethoxy-benzamide

[0248] 5-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-(tetrahydropyran-2-yloxy)-benzamide

Formula (II) Compound Table (Continued, Page 4 of 7)

[0249] 3,4-Difluoro-2-(4-bromo-2-methyl-phenylamino)-N-(3-phenylprop-2-ynyloxy)-benzamide

[0250] 3,4-Difluoro-2-(4-bromo-2-methyl-phenylamino)-N-(3-furylmethoxy)-benzamide

[0251] 3,4-Difluoro-2-(4-bromo-2-methyl-phenylamino)-N-(2-thienylmethoxy)-benzamide

[0252] 3,4-Difluoro-2-(4-bromo-2-methyl-phenylamino)-N-(but-3-ynyloxy)-benzamide

[0253] 3,4-Difluoro-2-(4-bromo-2-methyl-phenylamino)-N-(2-methyl-prop-2-enyloxy)-benzamide

[0254] 3,4-Difluoro-2-(4-bromo-2-methyl-phenylamino)-N-(but-2-enyloxy)-benzamide

[0255] 3,4-Difluoro-2-(4-bromo-2-methyl-phenylamino)-N-(methoxy)-benzamide

[0256] 3,4-Difluoro-2-(4-bromo-2-methyl-phenylamino)-N-(ethoxy)-benzamide

[0257] 3,4-Difluoro-2-(4-bromo-2-methyl-phenylamino)-N-(cyclobutoxy)-benzamide

[0258] 3,4-Difluoro-2-(4-bromo-2-methyl-phenylamino)-N-(isopropoxy)-benzamide

[0259] 3,4-Difluoro-2-(4-bromo-2-methyl-phenylamino)-N-(2-phenoxyethoxy)-benzamide

[0260] 3,4-Difluoro-2-(4-bromo-2-methyl-phenylamino)-N-(cyclopropylmethoxy)-benzamide

[0261] 3,4-Difluoro-2-(4-bromo-2-methyl-phenylamino)-N-(n-propoxy)-benzamide

[0262] 3,4-Difluoro-2-(4-bromo-2-methyl-phenylamino)-N-(1-methyl-prop-2-ynyloxy)-benzamide

[0263] 3,4-Difluoro-2-(4-bromo-2-methyl-phenylamino)-N-(3-(3-fluorophenyl)-prop-2-ynyloxy)-benzamide

[0264] 3,4-Difluoro-2-(4-bromo-2-methyl-phenylamino)-N-(4,4-dimethylpent-2-ynyloxy)-benzamide

Formula (II) Compound Table (Continued, Page 5 of 7)

[0265] 3,4-Difluoro-2-(4-bromo-2-methyl-phenylamino)-N-(cyclopentoxy)-benzamide

[0266] 3,4,5-Trifluoro-N-hydroxy-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0267] 5-Chloro-3,4-difluoro-N-hydroxy-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0268] 5-Bromo-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-hydroxy-benzamide

[0269] N-Hydroxy-2-(4-iodo-2-methyl-phenylamino)-4-nitro-benzamide

[0270] 3,4,5-Trifluoro-2-(2-fluoro-4-iodo-phenylamino)-N-hydroxy-benzamide

[0271] 5-Chloro-3,4-difluoro-2-(2-fluoro4-iodo-phenylamino)-N-hydroxy-benzamide

[0272] 5-Bromo-2-(2-chloro-4-iodo-phenylamino)-3,4-difluoro-N-hydroxy-benzamide

[0273] 2-(2-Fluoro-4-iodo-phenylamino)-N-hydroxy-4-nitro-benzamide

[0274] 2-(2-Chloro-4-iodo-phenylamino)-3,4,5-trifluoro-N-hydroxy-benzamide

[0275] 5-Chloro-2-(2-chloro-4-iodo-phenylamino)-3,4-difluoro-N-hydroxy-benzamide

[0276] 5-Bromo-2-(2-bromo-4-iodo-phenylamino)-3,4-difluoro-N-hydroxy-benzamide

[0277] 2-(2-Chloro-4-iodo-phenylamino)-N-hydroxy-4-methyl-benzamide

[0278] 2-(2-Bromo-4-iodo-phenylamino)-3,4,5-trifluoro-N-hydroxy-benzamide

[0279] 2-(2-Bromo-4-iodo-phenylamino)-5-chloro-3,4-difluoro-N-hydroxy-benzamide

[0280] 2-(2-Bromo-4-iodo-phenylamino)-N-hydroxy-4-nitro-benzamide

[0281] 4-Fluoro-2-(2-fluoro-4-iodo-phenylamino)-N-hydroxy-benzamide

[0282] 3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-hydroxy-benzamide

[0283] 2-(2-Chloro4-iodo-phenylamino)-4-fluoro-N-hydroxy-benzamide

[0284] 2-(2-Chloro-4-iodo-phenylamino)-3,4-difluoro-N-hydroxy-benzamide

[0285] 2-(2-Bromo-4-iodo-phenylamino)-4-fluoro-N-hydroxy-benzamide

[0286] 2-(2-Bromo-4-iodo-phenylamino)-3,4-difluoro-N-hydroxy-benzamide

Formula (II) Compound Table (Continued, Page 6 of 7)

[0287] N-Cyclopropylmethoxy-3,4,5-trifluoro-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0288] 5-Chloro-N-cyclopropylmethoxy-3,4-difluoro-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0289] 5-Bromo-N-cyclopropylmethoxy-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-benzamide

[0290] N-Cyclopropylmethoxy-2-(4-iodo-2-methyl-phenylamino)-4-nitro-benzamide

[0291] N-Cyclopropylmethoxy-3,4,5-trifluoro-2-(2-fluoro-4-iodo-phenylamino)-benzamide

[0292] 5-Chloro-N-cyclopropylmethoxy-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-benzamide

[0293] 5-Bromo-2-(2-chloro-4-iodo-phenylamino)-N-cyclopropylmethoxy-3,4-difluoro-benzamide

[0294] N-Cyclopropylmethoxy-2-(2-fluoro-4-iodo-phenylamino)-4-nitro-benzamide

[0295] 2-(2-Chloro-4-iodo-phenylamino)-N-cyclopropylmethoxy-3,4,5-trifluoro-benzamide

[0296] 5-Chloro-2-(2-chloro4-iodo-phenylamino)-N-cyclopropylmethoxy-3,4-difluoro-benzamide

[0297] 5-Bromo-2-(2-bromo4-iodo-phenylamino)-N-ethoxy-3,4-difluoro-benzamide

[0298] 2-(2-Chloro-4-iodo-phenylamino)-N-ethoxy-4-nitro-benzamide

[0299] 2-(2-Bromo-4-iodo-phenylamino)-N-cyclopropylmethoxy-3,4,5-trifluoro-benzamide

[0300] 2-(2-Bromo-4-iodo-phenylamino)-5-chloro-N-cyclopropylmethoxy-3,4-difluoro-benzamide

[0301] 2-(2-Bromo4-iodo-phenylamino)-N-cyclopropylmethoxy-4-nitro-benzamide

Formula (II) Compound Table (Continued, Page 7 of 7)

[0302] N-Cyclopropylmethoxy-4-fluoro-2-(2-fluoro4-iodo-phenylamino)-benzamide

[0303] N-Cyclopropylmethoxy-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-benzamide

[0304] 2-(2-Chloro4-iodo-phenylamino)-N-cyclopropylmethoxy-4-fluoro-benzamide

[0305] 2-(2-Chloro4-iodo-phenylamino)-N-cyclopropylmethoxy-3,4-difluoro-benzamide

[0306] 2-(2-Bromo-4-iodo-phenylamino)-N-cyclopropylmethoxy4-fluoro-benzamide

[0307] 2-(2-Bromo-4-iodo-phenylamino)-N-cyclopropylmethoxy-3,4-difluoro-benzamide.

[0308] In the most preferred embodiment of this invention, a compound selected from the following is administered to a patient (ie, a mammal) in an amount that is effective to prevent or treat rheumatoid arthritis or osteoarthritis:

[0309] 2-(2-Chloro-4-iodophenylamino)-N-cyclopropylmethoxy-3,4-difluorobenzamide (PD184352); 2-(2-Methyl4-iodophenylamino)-N-hydroxy-4-fluorobenzamide (PD170611); 2-(2-Methyl-4-iodophenylamino)-N-hydroxy-3,4-difluoro-5-bromobenzamide (PD171984); 2-(2-Methyl-4-iodophenylamino)-N-cyclopropylmethoxy-3,4-difluoro-5-bromobenzamide (PD177168); 2-(2-Methyl-4-iodophenylamino)-N-cyclobutylmethoxy-3,4-difluoro-5-bromobenzamide (PD 180841); 2-(2-Chloro-4-iodophenylamino)-N-cyclopropylmethoxy-3,4-difluoro-5-bromobenzamide (PD 184161); 2-(2-Chloro-4-iodophenylamino)-N-hydroxy-3,4-difluoro-5-bromobenzamide (PD184386); 2-(2-Chloro-4-iodophenylamino)-N-cyclobutylmethoxy-3,4-difluorobenzamide (PD 185625); 2-(2-Chloro-4-iodophenylamino)-N-hydroxy-4-fluorobenzamide (PD 185848); 2-(2-Methyl-4-iodophenylamino)-N-hydroxy-3,4-difluorobenzamide (PD 188563); 2-(2-Methyl4-iodophenylamino)-N-cyclopropylmethoxy-3,4,5-trifluorobenzamide (PD 198306); and 2-(2-Chloro-4-iodophenylamino)-N-cyclopropylmethoxy-4-fluorobenzamide (PD 203311); and the benzoic acid derivatives thereof. For example, the benzoic acid derivative of PD 198306 is 2-(2-Methyl-4-iodophenylamino)-3,4,5-trifluorobenzoic acid.

[0310] Additional preferred compounds include 2-(2-chloro-4-iodophenylamino)-5-chloro-N-cyclopropylmethoxy-3,4-difluorobenzamide (PD 297189), 2-(4-iodophenylamino)-N-cyclopropylmethoxy-5-chloro-3,4-difluorobenzamide (PD 297190), 2-(4-iodophenylamino)-5-chloro-3,4-difluorobenzoic acid (PD 296771), 2-(2-chloro4-iodophenylamino)-5-chloro-3,4-difluorobenzoic acid (PD 296770), 5-chloro-3,4-difluoro-2-(4-iodo-2-methylphenylamino)-benzoic acid (PD 296767); and 5-chloro-N-cyclopropylmethoxy-3,4-difluoro-2-(4-iodo-2-methylphenylamino)-benzamide (PD 298127).

[0311] The invention further provides methods of synthesis and synthetic intermediates.

[0312] Other features and advantages of the invention are apparent from the detailed description, examples, and claims set forth.

[0313] In a further preferred embodiment of this invention, a mitotic inhibitor is administered to a patient suffering from cancer and in need of treatment in combination with a selective MEK inhibitor selected from: 2-(2-Chloro-4-iodophenylamino)-N-cyclopropylmethoxy-3,4-difluorobenzamide (PD184352); 2-(2-Methyl-4-iodophenylamino)-N-hydroxy-4-fluorobenzamide (PD170611); 2-(2-Methyl-4-iodophenylamino)-N-hydroxy-3,4-difluoro-5-bromobenzamide (PD171984), a more preferred compound; 2-(2-Methyl-4-iodophenylamino)-N-cyclopropylmethoxy-3,4-difluoro-5-bromobenzamide (PD177168); 2-(2-Methyl-4-iodophenylamino)-N-cyclobutylmethoxy-3,4-difluoro-5-bromobenzamide (PD 180841); 2-(2-Chloro-4-iodophenylamino)-N-cyclopropylmethoxy-3,4-difluoro-5-bromobenzamide (PD 184161); 2-(2-Chloro-4-iodophenylamino)-N-hydroxy-3,4-difluoro-5-bromobenzamide (PD184386); 2-(2-Chloro-4-iodophenylamino)-N-cyclobutylmethoxy-3,4-difluorobenzamide (PD 185625); 2-(2-Chloro4-iodophenylamino)-N-hydroxy-4-fluorobenzamide (PD 185848); 2-(2-Methyl4-iodophenylamino)-N-hydroxy-3,4-difluorobenzamide (PD188563); 2-(2-Methyl-4-iodophenylamino)-N-cyclopropylmethoxy-3,4,5-trifluorobenzamide (PD 198306); and 2-(2-Chloro-4-iodophenylamino)-N-cyclopropylmethoxy-4-fluorobenzamide (PD 203311); and the benzoic acid derivatives thereof. For example, the benzoic acid derivative of PD 198306 is 2-(2-Methyl-4-iodophenylamino)-3,4,5-trifluorobenzoic acid.

DETAILED DESCRIPTION OF THE INVENTION

[0314] This invention provides a method of preventing or treating asthma in a patient which comprises administering to a patient suffering from asthma and in need of treatment, or to a patient at risk for developing an asthmatic attack, an anti-asthmatic effective amount of a MEK inhibitor. The invention provides a method of preventing and treating all forms of asthma and relieving the symptoms that accompany the disease. The invention is preferably practiced by administering a phenyl amine MEK inhibitor of Formula I or Formula II. Such MEK phenyl amine compounds are specific MEK 1 and MEK 2 inhibitors, meaning that they inhibit these enzymes without inhibiting other enzymes to a great extent.

[0315] The compounds of the present invention, which can be used to treat septic shock, are MEK inhibitors. A MEK inhibitor is a compound that shows MEK inhibition when tested in the assays titled “Enzyme Assays” in U.S. Pat. No. 5,525,625, column 6, beginning at line 35. The complete disclosure of U.S. Pat. No. 5,525,625 is hereby incorporated by reference. An example of a MEK inhibitor is 2-(2-amino-3-methoxyphenyl)-4-oxo-4H-[1]benzopyran. Specifically, a compound is a MEK inhibitor if a compound shows activity in the assay titled “Cascade Assay for Inhibitors of the MAP Kinase Pathway,” column 6, line 36 to column 7, line 4 of the U.S. Pat. No. 5,525,625 and/or shows activity in the assay titled “In Vitro MEK Assay” at column 7, lines 4 to 27 of the above-referenced patent.

[0316] A. Terms

[0317] Some of the terms used herein are defined below and by their usage throughout this disclosure.

[0318] The term “patient” means all animals including humans. Examples of patients include humans, cows, dogs, cats, goats, sheep, horses, and pigs. The mammals to be treated according to this invention are patients who have developed asthma and are suffering from the symptoms associated with disease, or who are at risk for developing the disease, for example having a family history of asthma. Those skilled in the medical art are readily able to identify individual patients, particularly children, who are afflicted with asthma, as well as those who are susceptible to developing the disease.

[0319] As used herein, the term “aryl” means a cyclic, bicyclic, or tricyclic aromatic ring moiety having from five to twelve carbon atoms. Examples of typical aryl groups include phenyl, naphthyl, and fluorenyl. The aryl may be substituted by one, two, or three groups selected from fluoro, chloro, bromo, iodo, alkyl, hydroxy, alkoxy, nitro, amino, alkylamino, or dialkylamino. Typical substituted aryl groups include 3-fluorophenyl, 3,5-dimethoxyphenyl, 4-nitronaphthyl, 2-methyl-4-chloro-7-aminofluorenyl, and the like.

[0320] The term “aryloxy” means an aryl group bonded through an oxygen atom, for example phenoxy, 3-bromophenoxy, naphthyloxy, and 4-methyl-1-fluorenyloxy.

[0321] “Heteroaryl” means a cyclic, bicyclic, or tricyclic aromatic ring moiety having from four to eleven carbon atoms and one, two, or three heteroatoms selected from O, S, or N. Examples include furyl, thienyl, pyrrolyl, pyrazolyl, imidazolyl, triazolyl, thiazolyl, oxazolyl, xanthenyl, pyronyl, indolyl, pyrimidyl, naphthyridyl, pyridyl, benzinnidazolyl, and triazinyl. The heteroaryl groups can be unsubstituted or substituted by one, two, or three groups selected from fluoro, chloro, bromo, iodo, alkyl, hydroxy, alkoxy, nitro, amino, alkylamino, or dialkylamino. Examples of substituted heteroaryl groups include chloropyranyl, methylthienyl, fluoropyridyl, amino-1,4-benzisoxazinyl, nitroisoquinolinyl, and hydroxyindolyl.

[0322] The heteroaryl groups can be bonded through oxygen to make heteroaryloxy groups, for example thienyloxy, isothiazolyloxy, benzofuranyloxy, pyridyloxy, and 4-methylisoquinolinyloxy.

[0323] The term “alkyl” means straight and branched chain aliphatic groups. Typical alkyl groups include methyl, ethyl, isopropyl, tert.-butyl, 2,3-dimethylhexyl, and 1,1-dimethylpentyl. The alkyl groups can be unsubstituted or substituted by halo, hydroxy, alkoxy, amino, alkylamino, dialkylamino, cycloalkyl, aryl, aryloxy, heteroaryl, or heteroaryloxy, as those terms are defined herein. Typical substituted alkyl groups include chloromethyl, 3-hydroxypropyl, 2-dimethylaminobutyl, and 2-(hydroxymethylamino)ethyl. Examples of aryl and aryloxy substituted alkyl groups include phenylmethyl, 2-phenylethyl, 3-chlorophenylmethyl, 1,1-dimethyl-3-(2-nitrophenoxy)butyl, and 3,4,5-trifluoronaphthylmethyl. Examples of alkyl groups substituted by a heteroaryl or heteroaryloxy group include thienylmethyl, 2-furylethyl, 6-furyloxyoctyl, 4-methylquinolyloxymethyl, and 6-isothiazolylhexyl. Cycloalkyl substituted alkyl groups include cyclopropylmethyl, 2-cyclohexyethyl, piperidyl-2-methyl, 2-(piperidin-1-yl)-ethyl, 3-(morpholin-4-yl)propyl.

[0324] “Alkenyl” means a straight or branched carbon chain having one or more double bonds. Examples include but-2-enyl, 2-methyl-prop-2-enyl, 1,1-dimethyl-hex-4-enyl, 3-ethyl-4-methyl-pent-2-enyl, and 3-isopropyl-pent-4-enyl. The alkenyl groups can be substituted with halo, hydroxy, alkoxy, amino, alkylamino, dialkylamino, aryl, aryloxy, heteroaryl, or heteroyloxy, for example 2-bromoethenyl, 3-hydroxy-2-butenyl, 1-aminoethenyl, 3-phenylprop-2-enyl, 6-thienyl-hex-2-enyl, 2-furyloxy-but-2-enyl, and 4-naphthyloxy-hex-2-enyl.

[0325] “Alkynyl” means a straight or branched carbon chain having at least one triple bond. Typical alkynyl groups include prop-2-ynyl, 2-methyl-hex-5-ynyl, 3,4-dimethyl-hex-5-ynyl, and 2-ethyl-but-3-ynyl. The alkynyl groups can be substituted as the alkyl and alkenyl groups, for example, by aryl, aryloxy, heteroaryl, or heteroaryloxy, for example 4-(2-fluorophenyl)-but-3-ynyl, 3-methyl-5-thienylpent-4-ynyl, 3-phenoxy-hex-4-ynyl, and 2-furyloxy-3-methyl-hex-4-ynyl.

[0326] The alkenyl and alkynyl groups can have one or more double bonds or triple bonds, respectively, or a combination of double and triple bonds. For example, typical groups having both double and triple bonds include hex-2-en-4-ynyl, 3-methyl-5-phenylpent-2-en-4-ynyl, and 3-thienyloxy-hex-3-en-5-ynyl.

[0327] The term “cycloalkyl” means a nonaromatic ring or fused rings. Examples include cyclopropyl, cyclobutyl, cyclopenyl, cyclooctyl, bicycloheptyl, adamantyl, and cyclohexyl. The ring can optionally contain one, two, or three heteroatoms selected from O, S, or N. Such groups include tetrahydrofuryl, tetrahydropyrrolyl, octahydrobenzofuranyl, morpholinyl, piperazinyl, pyrrolidinyl, piperidinyl, octahydroindolyl, and octahydrobenzothiofuranyl. The cycloalkyl groups can be substituted with the same substituents as an alkyl and alkenyl groups, for example, halo, hydroxy, aryl, and heteroaryloxy. Examples include 3-hydroxycyclohexyl, 2-aminocyclopropyl, 2-phenylpyrrolidinyl, and 3-thienylmorpholine-1-yl.

[0328] Selective MEK 1 or MEK 2 inhibitors are those compounds which inhibit the MEK 1 or MEK 2 enzymes, respectively, without substantially inhibiting other enzymes such as MKK3, PKC, Cdk2A, phosphorylase kinase, EGF, and PDGF receptor kinases, and C-src. In general, a selective MEK 1 or MEK 2 inhibitor has an IC50 for MEK 1 or MEK 2 that is at least one-fiftieth ({fraction (1/50)}) that of its IC50 for one of the above-named other enzymes. Preferably, a selective inhibitor has an IC50 that is at least {fraction (1/100)}, more preferably {fraction (1/500)}, and even more preferably {fraction (1/1000)}, {fraction (1/5000)}, or less than that of its IC50 or one or more of the above-named enzymes.

[0329] B. Administration and Formulation

[0330] The MEK inhibitors of the present method can be administered to a patient as part of a pharmaceutically acceptable composition. The compositions can be administered to humans and animals either orally, rectally, parenterally (intravenously, intramuscularly,or subcutaneously), intracisternally, intravaginally, intraperitoneally, intravesically, locally (powders, ointments, or drops), or as a buccal or nasal spray.

[0331] Compositions suitable for parenteral injection may comprise physiologically acceptable sterile aqueous or nonaqueous solutions, dispersions, suspensions or emulsions, and sterile powders for reconstitution into sterile injectable solutions or dispersions. Examples of suitable aqueous and nonaqueous carriers, diluents, solvents, or vehicles include water, ethanol, polyols (propyleneglycol, polyethyleneglycol, glycerol, and the like), suitable mixtures thereof, vegetable oils (such as olive oil), and injectable organic esters such as ethyl oleate. Proper fluidity can be maintained, for example, by the use of a coating such as lecithin, by the maintenance of the required particle size in the case of dispersions and by the use of surfactants.

[0332] These compositions may also contain adjuvants such as preserving, wetting, emulsifying, and dispensing agents. Prevention of the action of microorganisms can be ensured by various antibacterial and antifungal agents, for example, parabens, chlorobutanol, phenol, sorbic acid, and the like. It may also be desirable to include isotonic agents, for example sugars, sodium chloride, and the like. Prolonged absorption of the injectable pharmaceutical form can be brought about by the use of agents delaying absorption, for example, aluminum monostearate and gelatin.

[0333] Solid dosage forms for oral administration include capsules, tablets, pills, powders, and granules. In such solid dosage forms, the active compound is admixed with at least one inert customary excipient (or carrier) such as sodium citrate or dicalcium phosphate or (a) fillers or extenders, as for example, starches, lactose, sucrose, glucose, mannitol, and silicic acid, (b) binders, as for example, carboxymethylcellulose, alignates, gelatin, polyvinylpyrrolidone, sucrose, and acacia, (c) humectants, as for example, glycerol, (d) disintegrating agents, as for example, agar-agar, calcium carbonate, potato or tapioca starch, alginic acid, certain complex silicates, and sodium carbonate, (e) solution retarders, as for example paraffin, (f) absorption accelerators, as for example, quaternary ammonium compounds, (g) wetting agents, as for example, cetyl alcohol and glycerol monostearate, (h) adsorbents, as for example, kaolin and bentonite, and (i) lubricants, as for example, talc, calcium stearate, magnesium stearate, solid polyethylene glycols, sodium lauryl sulfate, or mixtures thereof. In the case of capsules, tablets, and pills, the dosage forms may also comprise buffering agents.

[0334] Solid compositions of a similar type may also be employed as fillers in soft and hard-filled gelatin capsules using such excipients as lactose or milk sugar as well as high molecular weight polyethyleneglycols, and the like.

[0335] Solid dosage forms such as tablets, dragees, capsules, pills, and granules can be prepared with coatings and shells, such as enteric coatings and others well-known in the art. They may contain opacifying agents, and can also be of such composition that they release the active compound or compounds in a certain part of the intestinal tract in a delayed manner. Examples of embedding compositions which can be used are polymeric substances and waxes. The active compounds can also be in micro-encapsulated form, if appropriate, with one or more of the above-mentioned excipients.

[0336] Liquid dosage forms for oral administration include pharmaceutically acceptable emulsions, solutions, suspensions, syrups, and elixirs. In addition to the active compounds, the liquid dosage forms may contain inert diluents commonly used in the art, such as water or other solvents, solubilizing agents and emulsifiers, as for example, ethyl alcohol, isopropyl alcohol, ethyl carbonate, ethyl acetate, benzyl alcohol, benzyl benzoate, propyleneglycol, 1,3-butyleneglycol, dimethylformamide, oils, in particular, cottonseed oil, groundnut oil, corn germ oil, olive oil, castor oil and sesame oil, glycerol, tetrahydrofurfuryl alcohol, polyethyleneglycols, and fatty acid esters of sorbitan or mixtures of these substances, and the like.

[0337] Besides such inert diluents, the composition can also include adjuvants, such as wetting agents, emulsifying and suspending agents, sweetening, flavoring, and perfuming agents.

[0338] Suspensions, in addition to the active compounds, may contain suspending agents, as for example, ethoxylated isostearyl alcohols, polyoxyethylene sorbitol and sorbitan esters, microcrystalline cellulose, aluminum metahydroxide, bentonite, agar-agar and tragacanth, or mixtures of these substances, and the like.

[0339] Compositions for rectal administrations are preferably suppositories which can be prepared by mixing the compounds of the present invention with suitable non-irritating excipients or carriers such as cocoa butter, polyethyleneglycol, or a suppository wax, which are solid at ordinary temperatures but liquid at body temperature and therefore, melt in the rectum or vaginal cavity and release the active component.

[0340] Dosage forms for topical administration of a compound of this invention include ointments, powders, sprays, and inhalants. The active component is admixed under sterile conditions with a physiologically acceptable carrier and any preservatives, buffers, or propellants as may be required. Ophthalamic formulations, eye ointments, powders, and solutions are also contemplated as being within the scope of this invention.

[0341] The compounds of the present method can be administered to a patient at dosage levels in the range of about 0.1 to about 1000 mg per day. For a normal human adult having a body weight of about 70 kg, a dosage in the range of about 0.01 to about 100 mg per kg of body weight per day is preferable. The specific dosage used, however, can vary. For example, the dosage can depend on a numbers of factors including the requirements of the patient, the severity of the condition being treated, and the pharmacological activity of the compound being used. The determination of optimum dosages for a particular patient is well-known to those skilled in the art.

[0342] The compounds of the present method can be administered as pharmaceutically acceptable salts, esters, amides, or prodrugs. The term “pharmaceutically acceptable salts, esters, amides, and prodrugs” as used herein refers to those carboxylate salts, amino acid addition salts, esters, amides, and prodrugs of the compounds of the present invention which are, within the scope of sound medical judgment, suitable for contact with the tissues of patients without undue toxicity, irritation, allergic response, and the like, commensurate with a reasonable benefit/risk ratio, and effective for their intended use, as well as the zwitterionic forms, where possible, of the compounds of the invention.

[0343] The term “salts” refers to the relatively non-toxic, inorganic and organic acid addition salts of compounds of the present invention. These salts can be prepared in situ during the final isolation and purification of the compounds or by separately reacting the purified compound in its free base form with a suitable organic or inorganic acid and isolating the salt thus formed. Representative salts include the hydrobromide, hydrochloride, sulfate, bisulfate, nitrate, acetate, oxalate, valerate, oleate, palmitate, stearate, laurate, borate, benzoate, lactate, phosphate, tosylate, citrate, maleate, fumarate, succinate, tartrate, naphthylate, mesylate, glucoheptonate, lactiobionate and laurylsulphonate salts, and the like. These may include cations based on the alkali and alkaline earth metals, such as sodium, lithium, potassium, calcium, magnesium and the like, as well as nontoxic ammonium, quaternary ammonium, and amine cations including, but not limited to ammonium, tetramethylammonium, tetraethylammonium, methylamine, dimethylamine, trimethylamine, triethylamine, ethylamine, and the like. (See, for example, S. M. Berge, et al., “Pharmaceutical Salts,” J. Pham. Sci., 1977;66:1-19 which is incorporated herein by reference.) Examples of pharmaceutically acceptable, non-toxic esters of the compounds of this invention include C1-C6 alkyl esters wherein the alkyl group is a straight or branched chain. Acceptable esters also include C5-C7 cycloalkyl esters as well as arylalkyl esters such as, but not limited to benzyl. C1-C4 alkyl esters are preferred. Esters of the compounds of the present invention may be prepared according to conventional methods.

[0344] Examples of pharmaceutically acceptable, non-toxic amides of the compounds of this invention include amides derived from ammonia, primary C1-C6 alkyl amines and secondary C1-C6 dialkyl amines wherein the alkyl groups are straight or branched chain. In the case of secondary amines the amine may also be in the form of a 5 or 6 membered heterocycle containing one nitrogen atom. Amides derived from ammonia, C1-C3 alkyl primary amines and C1-C2 dialkyl secondary amines are preferred. Amides of the compounds of the invention may be prepared according to conventional methods.

[0345] The term “prodrug” refers to compounds that are rapidly transformed in vivo to yield the parent compound of the above formula, for example, by hydrolysis in blood. A thorough discussion is provided in T. Higuchi and V. Stella, “Pro-drugs as Novel Delivery Systems,” Vol. 14 of the A.C.S. Symposium Series, and in Bioreversible Carriers in Drug Design, ed. Edward B. Roche, American Pharmaceutical Association and Pergamon Press, 1987, both of which are incorporated herein by reference.

[0346] In addition, the compounds of the present method can exist in unsolvated as well as solvated forms with pharmaceutically acceptable solvents such as water, ethanol, and the like. In general, the solvated forms are considered equivalent to the unsolvated forms for the purposes of the present invention.

[0347] Some of the compounds of the present method can exist in different stereoisometric forms by virtue of the presence of chiral centers. It is contemplated that all stereoisometric forms of the compounds as well as mixtures thereof, including racemic mixtures, form part of this invention.

[0348] C. Synthesis

[0349] The examples presented below are intended to illustrate particular embodiments of the invention and are not intended to limit the scope of the specification, including the claims, in any way. After the priority date of the present disclosure, related syntheses and MEK inhibition data were also published in WO 99/01421 and WO 99/01426, hereby incorporated by reference.

[0350] The 2-(4-bromo and 4-iodo phenylamino)-benzoic acid derivatives of Formula I can be prepared from commercially available starting materials utilizing synthetic methodologies well-known to those skilled in organic chemistry. A typical synthesis is carried out by reacting a 4-bromo or 4-iodo aniline with a benzoic acid having a leaving group at the 2-position to give a 2-(phenylamino)-benzoic acid. This process is depicted in Scheme 1. 4

[0351] where L is a leaving group, for example halo such as fluoro.

[0352] The reaction of aniline and the benzoic acid derivative generally is accomplished by mixing the benzoic acid with an equimolar quantity or excess of the aniline in an unreactive organic solvent such as tetrahydrofuran or toluene, in the presence of a base such as lithium diisopropylamide, n-butyl lithium, sodium hydride, triethylamine, and Hunig's base. The reaction generally is carried out at a temperature of about −78° C. to about 100° C., and normally is complete within about 2 hours to about 4 days. The product can be isolated by removing the solvent, for example by evaporation under reduced pressure, and further purified, if desired, by standard methods such as chromatography, crystallization, or distillation.

[0353] The 2-(phenylamino)-benzoic acid (e.g., Formula I, where R7 is hydrogen) can be reacted with an organic or inorganic base such as pyridine, triethylamine, calcium carbonate, or sodium hydroxide to produce a pharmaceutically acceptable salt. The free acids can also be reacted with an alcohol of the formula HOR7 (where R7 is other than hydrogen, for example methyl) to produce the corresponding ester. Reaction of the benzoic acid with an alcohol can be carried out in the presence of a coupling agent. Typical coupling reagents include 2-ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline (EEDQ), 1,3-dicyclohexylcarbodiimide (DCC), bromo-tris(pyrrolidino)-phosphonium hexafluorophosphate (PyBrOP), and (benzotriazolyloxy) tripyrrolidino phosphonium hexafluorophosphate (PyBOP). The phenylamino benzoic acid and alcohol derivative normally are mixed in approximately equimolar quantities in an unreactive organic solvent such as dichloromethane, tetrahydrofuran, chloroform, or xylene, and an equimolar quantity of the coupling reagent is added. A base such as triethylamine or diisopropylethylamine can be added to act as an acid scavenger if desired. The coupling reaction generally is complete after about 10 minutes to 2 hours, and the product is readily isolated by removing the reaction solvent, for instance by evaporation under reduced pressure, and purifying the product by standard methods such as chromatography or crystallizations from solvents such as acetone, diethyl ether, or ethanol.

[0354] The benzamides of the invention, Formula I where Z is CONR6R7, are readily prepared by reacting the foregoing benzoic acids with an amine of the formula HNR6R7. The reaction is carried out by reacting approximately equimolar quantities of the benzoic acid and amine in an unreactive organic solvent in the presence of a coupling reagent. Typical solvents are chloroform, dichloromethane, tetrahydrofuran, benzene, toluene, and xylene. Typical coupling reagents include DCC, EEDQ, PyBrOP, and PyBOP. The reaction is generally complete after about 10 minutes to about 2 hours when carried out at a temperature of about 0° C. to about 60° C. The product amide is readily isolated by removing the reaction solvent, for instance by evaporation, and further purification can be accomplished by normal methods such as chromatography, crystallization, or distillation. The hydrazides (z=CONHNR10R11) are similarly prepared by coupling a benzoic acid with a hydrazine of the formula

H2HNR10R11.

[0355] The benzyl alcohols of the invention, compounds of Formula I where Z is CH2OR6 and R6 is hydrogen, are readily prepared by reduction of the corresponding benzoic acid according to the following Scheme 2. 5

[0356] Typical reducing agents commonly employed include borane in tetrahydrofuran. The reduction normally is carried out in an unreactive organic solvent such as tetrahydrofuran, and generally is complete within about 2 hours to about 24 hours when conducted at a temperature of about 0° C. to about 40° C.

[0357] The following detailed examples illustrate specific compounds provided by this invention.

EXAMPLE 1

4-Fluoro-2-(4-iodo-2-methylphenylamino)benzoic acid

[0358] To a stirring solution comprised of 3.16 g (0.0133 mol) of 2-amino-5-iodotoluene in 5 mL of tetrahydrofuran at −78° C. was added 10 mL (0.020 mol) of a 2.0 M lithium diisopropylamide in tetrahydrofuran/heptane/ethenylbenzene (Aldrich) solution. The resulting green suspension was stirred vigorously for 15 minutes, after which time a solution of 1.00 g (0.00632 mol) of 2,4-difluorobenzoic acid in 10 mL of tetrahydrofuran was added. The reaction temperature was allowed to increase slowly to room temperature, at which temperature it was stirred for 2 days. The reaction mixture was concentrated. Aqueous HCl (10%) was added to the concentrate, and the solution was extracted with dichloromethane. The organic phase was dried (MgSO4) and then boiled over a steambath to low volume and cooled to room temperature. The off-white fibers were collected by vacuum filtration, rinsed with hexanes, and vacuum-oven dried. (76° C.; ca. 10 mm of Hg) to afford 1.10 g (47%) of the desired material;

[0359] mp 224-229.5° C.; 1H NMR (400 MHz; DMSO): δ 9.72 (s, 1H), 7.97 (dd, 1H, J=7.0, 8.7 Hz), 7.70 (d, 1H, J=1.5 Hz), 7.57 (dd, 1H, J=8.4, 1.9 Hz), 7.17 (d, 1H, J=8.2 Hz), 6.61-6.53 (m, 2H), 2.18 (s, 3H); 13C NMR (100 MHz; DMSO): δ 169.87, 167.60, 165.12, 150.17, 150.05, 139.83, 138.49, 136.07, 135.31, 135.20, 135.07, 125.60, 109.32, 105.09, 104.87, 99.72, 99.46, 89.43, 17.52; 19F NMR (376 MHz; DMSO): δ −104.00 to −104.07 (m); IR (KBr) 1670 (C═O stretch) cm−1; MS (CI) M+1=372. Analysis calculated for C14H11FINO2: C, 45.31; H, 2.99; N, 3.77. Found: C, 45.21; H, 2.77; N, 3.64.

EXAMPLES 2-30

[0360] By following the general procedure of Example 1, the following benzoic acids and salts of Formula (I) were prepared.

Example
No.	Compound	MP° C.
2	3,4,5-Trifluoro-2-(4-iodo-2-methyl-phenylamino)-	206-210
	benzoic acid
3	3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-benzoic	240.5-244.5
	acid
4	5-Bromo-3,4-difluoro-2-(4-iodo-2-methyl-	259.5-262
	phenylamino)-benzoic acid
5	5-Chloro-2-(2-chloro-4-iodo-phenylamino)-benzoic acid	255-260
6	5-Chloro-2-(4-iodo-2-methyl-phenylamino)-benzoic acid	234-238
7	Sodium 5-Chloro-2-(4-iodo-2-methyl-phenylamino)-	310-320
	benzoate	DEC
8	5-Bromo-2-(4-iodo-2-methyl-phenylamino)-benzoic acid	239.5-240
9	2-(2-Chloro-4-iodo-phenylamino)-5-nitro-benzoic acid	289-293
10	4-Fluoro-2-(3-fluoro-4-iodo-2-methyl-phenylamino)-	233-235
	benzoic acid
11	2-(4-Iodo-2-methyl-phenylamino)-5-nitro-benzoic acid	264-267
12	2-(2-Fluoro-4-iodo-phenylamino)-5-nitro-benzoic acid	256-258
13	2-(4-Bromo-2-methyl-phenylamino)-4-fluoro-benzoic	218.5-220
	acid
14	2-(2-Bromo-4-iodo-phenylamino)-5-nitro-benzoic acid	285-288
		DEC
15	2-(4-Bromo-2-methyl-phenylamino)-3,4-difluoro-	230-234
	benzoic acid
16	3-Fluoro-2-(4-iodo-2-methyl-phenylamino)-benzoic acid	218-221
17	3,4-Difluoro-2-(4-iodo-2-methoxy-phenylamino)-	230-233
	benzoic acid
18	4-Chloro-2-(4-iodo-2-methyl-phenylamino)-benzoic acid	245-255
		DEC
19	2-(4-Iodo-2-methyl-phenylamino)-benzoic acid	218-223
20	5-Fluoro-2-(4-iodo-2-methyl-phenylamino)-benzoic acid	243-46
21	5-Iodo-2-(4-iodo-2-methyl-phenylamino)-benzoic acid	241-245
22	2,3,5-Trifluoro-4-(4-iodo-2-methyl-phenylamino)-	218-222
	benzoic acid
23	4-Fluoro-2-(3-chloro-4-iodo-2-methyl-phenylamino)-	248-252.5
	benzoic acid
24	2-(4-Iodo-phenylamino)-5-methoxy-benzoic acid	208-211
25	3-Chloro-2-(2-chloro-4-iodo-phenylamino)-benzoic acid	232-233
26	2-Fluoro-6-(4-iodo-2-methyl-phenylamino)-benzoic acid	179-182
27	4-Fluoro2-(2,3-dimethyl-4-iodo-2-methyl-	258-261
	phenylamino)benzoic acid
28	5-Methyl-2-(4-iodo-2-methyl-phenylamino)-benzoic	209.5-211
	acid
29	2-Chloro-6-(4-iodo-2-methyl-phenylamino)-benzoic acid	171-175
30	2-(4-Iodo-2-methyl-phenylamino)-4-nitro-benzoic acid	251-263

EXAMPLE 31

5Chloro-N-(2-hydroxyethyl)-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0361] To a stirring solution comprised of 0.1020 g (0.2632 mmol) of 5-chloro-2-(4-iodo-2-methyl-phenylamino)-benzoic acid, 0.1 mL (1.7 mmol) of ethanolamine, and 0.05 mL (0.29 mmol) of diisopropylethylamine in 5 mL of a 1:1 (v/v) tetrahydrofuran-dichloromethane solution was added 0.15 g (0.29 mmol) of solid PyBOP powder directly. The reaction mixture was stirred at room temperture overnight. The solvent was removed in vacuo. The crude residue was partitioned between ether (50 mL) and 10% aqueous hydrochloric acid (50 mL). The organic phase was washed with 10% aqueous sodium hydroxide (50 mL), dried SO4) and concentrated in vacuo to afford a yellow-brown oil which was crystallized from hexanes-ether to afford 0.0831 g (73%) of a green-yellow power; mp 120-121° C.;

[0362] 1 H NMR (400 MHz; CDCl3): δ 9.11 (s, 1H), 7.56 (d, 1H, J=1.4 Hz), 7.46-7.41 (m, 2H), 7.20 (dd, 1H, J=8.9, 2.4 Hz), 7.00 (t, 2H, J=9.6 Hz), 6.55 (broad t, 1H), 3.86 (t, 2H, J=5.0 Hz), 3.61 (dd, 2H, J=10.1, 5.5 Hz), 2.23 (s, 3H), 1.56 (broad s, 1H); IR (KBr) 3297 (O—H stretch), 1627 (C═O stretch) cm−1; MS (CI) M+1=431. Analysis calculated for C16H16ClIN2O2: C, 44.62; H, 3.74; N, 6.50. Found: 44.63; H, 3.67; N, 6.30.

EXAMPLES 32-48

[0363] By following the general procedure of Example 31, the following benzamides were prepared by reacting the corresponding benzoic acid with the corresponding amine.

Example
No.	Compound	MP° C.
32	4-Methoxy-N-(4-methoxy-phenyl)-3-nitro-	153.5-156
	benzamide
33	4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-	158
	benzamide
34	4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-	102.5-104.5
	methyl-benzamide
35	N-Ethyl-4-fluoro-2-(4-iodo-2-methyl-phenylamino)-	90-91
	benzamide
36	4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N,N-	oil
	dimethyl-benzamide
37	4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-(1H-	285-288
	tetrazol-5-yl)-benzamide	DEC
38	5-Bromo-2-(4-iodo-2-methyl-phenylamino)-	180-182
	benzamide
39	5-Chloro-2-(4-iodo-2-methyl-phenylamino)-N,N-	137-138
	dimethyl-benzamide
40	[5-Chloro-2-(4-iodo-2-methyl-phenylamino)-	170-173
	benzoylamino]-acetic acid
41	4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-	69-71
	propyl-benzamide
42	5-Bromo-N-(2-hydroxy-ethyl)-2-(4-iodo-2-methyl-	132-133.4
	phenylamino)-benzamide
43	N,N-Diethyl-4-fluoro-2-(4-iodo-2-methyl-	oil
	phenylamino)-benzamide
44	4-Fluoro-N-{3-[4-(2-hydroxy-ethyl)-piperazin-1-yl]-	122-124
	propyl}-2-(4-iodo-2-methyl-phenylamino)-
	benzamide
45	N,N-Diethyl-2-(4-iodo-2-methyl-phenylamino)-5-	91-93
	nitro-benzamide
46	N-Butyl-4-fluoro-2-(4-iodo-2-methyl-phenylamino)-	97-99
	benzamide
47	5-Chloro-N,N-diethyl-2-(4-iodo-2-methyl-	118-120
	phenylamino)-benzamide
48	5-Bromo-2-(4-iodo-2-methyl-phenylamino)-N,N-	142.5-144
	dimethyl-benzamide

EXAMPLE 49

4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-benzyl alcohol

[0364] 4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-benzoic acid (0.50 g, 1.35 mmol) was dissolved in 6 mL (6 mmol) of cold 1.0 M borane-tetrahydrofuran complex in tetrahydrofuran solution. The reaction mixture was stirred under nitrogen atmosphere at room temperature overnight. The reaction was quenched with 80 mL of methanol. Concentration in vacuo produced a clear tan oil which was purified by MPLC. Elution with dichloromethane afforded 0.4285 g 89%) of a white solid; mp 99-100.5° C.;

[0365] 1 H NMR (400 MHz; DMSO): δ 7.57 (d, 1H, J=1.7 Hz), 7.45 (dd, 1H, J=8.4, 1.9 Hz), 7.39 (s, 1H), 7.29 (t, 1H, J=7.5 Hz), 6.89 (d, 1H, J=8.4 Hz), 6.67-6.60 (m, 1H), 5.47 (t,1H, J=5.5 Hz), 4.49 (d, 2H, 5.1 Hz), 2.14 (s, 3H); IR (KBr) 3372 (O—H stretch) cm−1; MS (CI) M+1=358. Analysis calculated for C14H13FINO: C, 47.08; H, 3.67; N, 3.92. Found: C, 47.17; H, 3.75; N, 3.72.

EXAMPLE 50-52

[0366] The following benzyl alcohols were prepared by the general procedure of Example 49.

Example
No.	Compound	MP° C.
50	[5-Chloro-2-(4-iodo-2-methyl-phenylamino)-	82-85
	phenyl]-methanol
51	[2-(4-Iodo-2-methyl-phenylamino)-5-nitro-phenyl]-	126.5-128.5
	methanol
52	[5-Bromo-2-(4-iodo-2-methyl-phenylamino)-	60.5-63.5
	phenyl]-methanol

[0367] Several invention compounds of Formula I were prepared utilizing combinatorial synthetic techniques. The general procedure is as follows:

[0368] To a 0.8-mL autosampler vial in a metal block was added 40 μL of a 0.5 M solution of the acid in DMF and 40 μL of the reagent amine (2 M solution in Hunig's base and 1 M in amine in DMF). A 0.5 M solution of PyBrop was freshly prepared and 50 μL were added to the autosampler vial. The reaction was allowed to stand for 24 hours.

[0369] The reaction mixture was transferred to a 2-dram vial and diluted with 2 mL of ethyl acetate. The organic layer was washed with 3 mL of distilled water and the water layer washed again with 2 mL of ethyl acetate. The combined organic layers were allowed to evaporate to dryness in an open fume hood.

[0370] The residue was taken up in 2 mL of 50% acetonitrile in water and injected on a semi-prep reversed phase column (10 mm×25 cm, 5 μM spherical silica, pore size 115 A derivatized with C-18, the sample was eluted at 4.7 mL/min with a linear ramp to 100% acetonitrile over 8.5 minutes. Elution with 100% acetonitrile continued for 8 minutes). Fractions were collected by monitoring at 214 nM. The residue was dissolved in chloroform and transferred to a preweighed vial, evaporated, and weighed again to determine the yield.

EXAMPLES 53-206

[0371] The following compounds of Formula I were prepared by combinatorial methodology:

Example		MS
No.	Compound	M − H
53	5-Bromo-3,4-difluoro-N-(2-hydroxy-ethyl)-2-(4-iodo-2-methyl-	510
	phenylamino)-benzamide
54	N-(2,3-Dihydroxy-propyl)-3,4-difluoro-2-(4-iodo-2-methyl-	462
	phenylamino)-benzamide
55	5-Bromo-3,4-difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(2-	577
	piperidin-1-yl-ethyl)-benzamide
56	3,4-Difluoro-N-(2-hydroxy-ethyl)-2-(4-iodo-2-methyl-	432
	phenylamino)-benzamide
57	N-(2,3-Dihydroxy-propyl)-4-fluoro-2-(4-iodo-2-methyl-	444
	phenylamino)-benzamide
58	3,4-Difluoro-N-(3-hydroxy-propyl)-2-(4-iodo-2-methyl-	446
	phenylamino)-benzamide
59	5-Bromo-3,4-difluoro-2-(4-iodo-2-methyl-phenylamino)-N-	564
	(2-pyrrolidin-1-yl-ethyl)-benzamide
60	5-Bromo-3,4-difluoro-2-(4-iodo-2-methyl-phenylamino)-N-	571
	(2-pyridin-4-yl-ethyl)-benzamide
61	4-Fluoro-N-(2-hydroxy-ethyl)-2-(4-iodo-2-methyl-phenylamino)-	414
	benzamide
62	5-Bromo-N-(3-dimethylamino-propyl)-3,4-difluoro-2-(4-iodo-	551
	2-methyl-phenylamino)-benzamide
63	5-Bromo-3,4-difluoro-2-(4-iodo-2-methyl-phenylamino)-N-	580
	(2-morpholin-4-yl-ethyl)-benzamide
64	3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(2-morpholin-	501
	4-yl-ethyl)-benzamide
65	3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(2-pyrrolidin-	485
	1-yl-ethyl)-benzamide
66	3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(2-pyridin-4-yl-	493
	ethyl)-benzamide
67	N-(3-Dimethylamino-propyl)-3,4-difluoro-2-(4-iodo-2-methyl-	473
	phenylamino)-benzamide
68	N-Benzyl-4-fluoro-2-(4-iodo-2-methyl-phenylamino)-benzamide	460
69	2-(4-Bromo-2-methyl-phenylamino)-3,4-difluoro-N-(2-hydroxy-	384
	ethyl)-benzamide
70	4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-(2-morpholin-4-yl-	483
	ethyl)-benzamide
71	4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-(3-piperidin-1-yl-	495
	propyl)-benzamide
72	3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-N-(3-piperidin-	513
	1-yl-propyl)-benzamide
73	4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-(2-thiophen-2-yl-	480
	ethyl)-benzamide
74	4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-(2-pyrrolidin-1-yl-	467
	ethyl)-benzamide
75	2-(4-Bromo-2-methyl-phenylamino)-3,4-difluoro-N-(2-morpholin-	453
	4-yl-ethyl)-benzamide
76	5-Bromo-3,4-difluoro-2-(4-iodo-2-methyl-phenylamino)-N-	557
	pyridin-4-ylmethyl-benzamide
77	3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-N-pyridin-	479
	4-ylmethyl-benzamide
78	2-(4-Bromo-2-methyl-phenylamino)-N-(3-dimethylamino-propyl)-	425
	3,4-difluoro-benzamide
79	4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-pyridin-4-ylmethyl-	461
	benzamide
80	4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-(2-pyridin-4-yl-	475
	ethyl)-benzamide
81	2-(4-Bromo-2-methyl-phenylamino)-3,4-difluoro-N-(2-pyridin-	445
	4-yl-ethyl)-benzamide
82	2-(4-Bromo-2-methyl-phenylamino)-3,4-difluoro-N-(3-hydroxy-	400
	propyl)-benzamide
83	2-(4-Bromo-2-methyl-phenylamino)-3,4-difluoro-N-(2-pyrrolidin-	437
	1-yl-ethyl)-benzamide
84	4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-phenethyl-	474
	benzamide
85	2-(4-Bromo-2-methyl-phenylamino)-3,4-difluoro-N-(2-thiophen-	450
	2-yl-ethyl)-benzamide
86	2-(4-Bromo-2-methyl-phenylamino)-3,4-difluoro-N-pyridin-	431
	4-ylmethyl-benzamide
87	2-(4-Bromo-2-methyl-phenylamino)-3,4-difluoro-N-phenethyl-	444
	benzamide
88	2-(4-Bromo-2-methyl-phenylamino)-3,4-difluoro-N-(2-piperidin-	451
	1-yl-ethyl)-benzamide
89	5-Chloro-N-{3-[4-(2-hydroxy-ethyl)-piperazin-1-yl]-propyl}-	557*
	2-(4-iodo-2-methyl-phenylamino)- benzamide
90	5-Fluoro-N-{3-[4-(2-hydroxy-ethyl)-piperazin-1-yl]-propyl}-	541*
	2-(4-iodo-2-methyl- phenylamino)- benzamide
91	2-(4-Iodo-2-methyl-phenylamino)-5-nitro-N-pyridin-4-yl methyl-	487
	benzamide
92	5-Bromo-N-{ 3-[4-(2-hydroxy-ethyl)-piperazin-1-yl]-propyl}-	601*
	2-(4-iodo-2-methyl- phenylamino)- benzamide
93	5-Chloro-N-(2-diethylamino-ethyl)-2-(4-iodo-2-methyl-	486*
	phenylamino)- benzamide
94	5-Chloro-2-(4-iodo-2-methyl-phenylamino)-N-(2-piperidin-1-yl-	497*
	ethyl)-benzamide
95	(3-Hydroxy-pyrrolidin-1-yl)-[2-(4-iodo-2-methyl-phenylamino)-	466
	5-nitro-phenyl]-methanone
96	5-Chloro-2-(4-iodo-2-methyl-phenylamino)-N-(2-pyrrolidin-1-yl-	484*
	ethyl)-benzamide
97	5-Bromo-N-(2-diethylamino-ethyl)-2-(4-iodo-2-methyl-	530*
	phenylamino)- benzamide
98	N-{2-[Bis-(2-hydroxy-ethyl)-amino]-ethyl}-5-chloro-2-(4-iodo-	518*
	2-methyl- phenylamino)- benzamide
99	N-{2-[Bis-(2-hydroxy-ethyl)-amino]-ethyl}-5-bromo-2-(4-iodo-	562*
	2-methyl- phenylamino)- benzamide
100	[5-Bromo-2-(4-iodo-2-methyl-phenylamino)-phenyl]-(3-hydroxy-	499
	pyrrolidin-1-yl)-methanone
101	2-(4-Iodo-2-methyl-phenylamino)-5-nitro-benzoic acid phenethyl	501
	ester
102	N-{3-[4-(2-Hydroxy-ethyl)-piperazin-1-yl]-propyl }-2-(4-iodo-	568*
	2-methyl-phenylamino)- benzamide
103	[5-Chloro-2-(4-iodo-2-methyl-phenylamino)-phenyl]-(3-hydroxy-	455
	pyrrolidin-1-yl)-methanone
104	5-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-pyridin-4-ylmethyl-	460
	benzamide
105	5-Bromo-2-(4-iodo-2-methyl-phenylamino)-N-(2-pyrrolidin-1-yl-	528*
	ethyl)-benzamide
106	5-Bromo-2-(4-iodo-2-methyl-phenylamino)-N-(2-piperidin-1-yl-	542*
	ethyl)-benzamide
107	5-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-(2-pyrrolidin-1-yl-	468*
	ethyl)-benzamide
108	5-Chloro-N-(3-dimethylamino-propyl)-2-(4-iodo-2-methyl-	472*
	phenylamino)-benzamide
109	N-{2-[Bis-(2-hydroxy-ethyl)-amino]-ethyl}-5-fluoro-2-(4-iodo-	502*
	2-methyl- phenylamino)- benzamide
110	5-Chloro-N-(3-hydroxy-propyl)-2-(4-iodo-2-methyl-	445*
	phenylamino)-benzamide
111	5-Chloro-N-(3-diethylamino-2-hydroxy-propyl)-2-(4-iodo-	516*
	2-methyl-phenylamino)- benzamide
112	5-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-(2-piperidin-1-yl-	482*
	ethyl)-benzamide
113	5-Bromo-N-(3-hydroxy-propyl)-2-(4-iodo-2-methyl-	489*
	phenylamino)-benzamide
114	5-Bromo-2-(4-iodo-2-methyl-phenylamino)-N-(3-piperidin-1-yl-	556*
	propyl)-benzamide
115	N-{2-[Bis-(2-hydroxy-ethyl)-amino]-ethyl}-2-(4-iodo-2-methyl-	529*
	phenylamino)-5-nitro-benzamide
116	5-Chloro-2-(4-iodo-2-methyl-phenylamino)-N-(2-morpholin-4-yl-	500*
	ethyl)-benzamide
117	5-Chloro-N-(3-diethylamino-propyl)-2-(4-iodo-2-methyl-	500*
	phenylamino)-benzamide
118	5-Chloro-N-(2-diisopropylamino-ethyl)-2-(4-iodo-2-methyl-	514*
	phenylamino)-benzamide
119	5-Chloro-2-(4-iodo-2-methyl-phenylamino)-N-(3-piperidin-1-yl-	512*
	propyl)-benzamide
120	2-(4-Iodo-2-methyl-phenylamino)-5-nitro-N-(2-piperidin-1-yl-	509*
	ethyl)-benzamide
121	5-Bromo-2-(4-iodo-2-methyl-phenylamino)-N-(2-piperazin-1-yl-	544*
	ethyl)-benzamide
122	N-(2-Diethylamino-ethyl)-5-fluoro-2-(4-iodo-2-methyl-	470*
	phenylamino)-benzamide
123	5-Bromo-N-(3-dimethylamino-propyl)-2-(4-iodo-2-methyl-	516*
	phenylamino)-benzamide
124	N-(3-Hydroxy-propyl)-2-(4-iodo-2-methyl-phenylamino)-5-nitro-	456*
	benzamide
125	5-Fluoro-N-(3-hydroxy-propyl)-2-(4-iodo-2-methyl-	429*
	phenylamino)-benzamide
126	N-(3-Diethylamino-propyl)-5-fluoro-2-(4-iodo-2-methyl-	484*
	phenylamino)-benzamide
127	N-(3-Diethylamino-propyl)-2-(4-iodo-2-methyl-phenylamino)-	511*
	5-nitro-benzamide
128	5-Bromo-2-(4-iodo-2-methyl-phenylamino)-N-(2-morpholin-4-yl-	544*
	ethyl)-benzamide
129	2-(4-Iodo-2-methyl-phenylamino)-5-nitro-N-(3-piperidin-1-yl-	523*
	propyl)-benzamide
130	[5-Fluoro-2-(4-iodo-2-methyl-phenylamino)-phenyl]-(3-hydroxy-	439
	pyrrolidin-1-yl)-methanone
131	5-Bromo-N-(2-diisopropylamino-ethyl)-2-(4-iodo-2-methyl-	558*
	phenylamino)-benzamide
132	5-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-(2-morpholin-4-yl-	484*
	ethyl)-benzamide
133	5-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-(3-piperidin-1-yl-	496*
	propyl)-benzamide
134	[5-Fluoro-2-(4-iodo-2-methyl-phenylamino)-phenyl]-	482
	[4-(2-hydroxy-ethyl)-piperazin-1-yl]-methanone
135	N-(3-Diethylamino-2-hydroxy-propyl)-5-fluoro-2-(4-iodo-	500*
	2-methyl-phenylamino)-benzamide
136	[5-Chloro-2-(4-iodo-2-methyl-phenylamino)-benzoylamino]-	443
	acetic acid
137	2-(4-Iodo-2-methyl-phenylamino)-5-nitro-N-(2-pyrrolidin-1-yl-	495*
	ethyl)-benzamide
138	N-(3-Dimethylamino-propyl)-2-(4-iodo-2-methyl-phenylamino)-	483*
	5-nitro-benzamide
139	N-(2-Diisopropylamino-ethyl)-5-fluoro-2-(4-iodo-2-methyl-	498*
	phenylamino)- benzamide
140	5-Fluoro-2-(4-iodo-2-methyl-phenylamino)-thiobenzoic acid S-	490
	phenethyl ester
141	5-Chloro-2-(4-iodo-2-methyl-phenylamino)-thiobenzoic acid S-	506
	phenethyl ester
142	5-Bromo-2-(4-iodo-2-methyl-phenylamino)-thiobenzoic acid S-	536
	benzyl ester
143	2-(4-Iodo-2-methyl-phenylamino)-5-nitro-thiobenzoic acid S-	503
	benzyl ester
144	5-Fluoro-2-(4-iodo-2-methyl-phenylamino)-thiobenzoic acid S-	476
	benzyl ester
145	5-Chloro-2-(4-iodo-2-methyl-phenylamino)-thiobenzoic acid S-	492
	benzyl ester
146	N-Cyclopropyl-5-fluoro-2-(4-iodo-2-methyl-phenylamino)-	409
	benzamide
147	5-Chloro-N-(2-hydroxy-ethyl)-2-(4-iodo-2-methyl-phenylamino)-	429
	benzamide
148	5-Fluoro-N-(2-hydroxy-ethyl)-2-(4-iodo-2-methyl-phenylamino)-	413
	benzamide
149	N-Benzyloxy-5-fluoro-2-(4-iodo-2-methyl-phenylamino)-	475
	benzamide
150	N-Benzyloxy-5-bromo-2-(4-iodo-2-methyl-phenylamino)-	593*
	benzamide
151	2-(4-Iodo-2-methyl-phenylamino)-5-nitro-N-(4-sulfamoyl-	567
	benzyl)-benzamide
152	5-Bromo-N-(2-hydroxy-ethyl)-2-(4-iodo-2-methyl-phenylamino)-	473
	benzamide
153	N-(2-Hydroxy-ethyl)-5-iodo-2-(4-iodo-2-methyl-phenylamino)-	521
	benzamide
154	N-(2-Hydroxy-ethyl)-2-(4-iodo-2-methyl-phenylamino)-5-nitro-	440
	benzamide
155	2-(4-Iodo-2-methyl-phenylamino)-N-methyl-5-nitro-N-phenyl-	486
	benzamide
156	5-Chloro-N-cyclopropyl-2-(4-iodo-2-methyl-phenylamino)-	425
	benzamide
157	5-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-methyl-N-phenyl-	459
	benzamide
158	N-Allyl-5-fluoro-2-(4-iodo-2-methyl-phenylamino)-benzamide	409
159	N-Benzyloxy-5-iodo-2-(4-iodo-2-methyl-phenylamino)-	583
	benzamide
160	5-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-(4-sulfamoyl-	538
	benzyl)-benzamide
161	N-Allyl-5-chloro-2-(4-iodo-2-methyl-phenylamino)-benzamide	425
162	N-Cyclopropyl-2-(4-iodo-2-methyl-phenylamino)-5-nitro-	436
	benzamide
163	5-Bromo-N-cyclopropyl-2-(4-iodo-2-methyl-phenylamino)-	469
	benzamide
164	5-Chloro-2-(4-iodo-2-methyl-phenylamino)-N-methyl-N-phenyl-	475
	benzamide
165	5-Iodo-2-(4-iodo-2-methyl-phenylamino)-N-(4-sulfamoyl-benzyl)-	646
	benzamide
166	5-Bromo-2-(4-iodo-2-methyl-phenylamino)-N-(4-sulfamoyl-	598
	benzyl)-benzamide
167	N-Allyl-2-(4-iodo-2-methyl-phenylamino)-5-nitro-benzamide	436
168	2-(4-Iodo-2-methyl-phenylamino)-5-nitro-N-(4-sulfamoyl-	565
	benzyl)-benzamide
169	N-Allyl-5-bromo-2-(4-iodo-2-methyl-phenylamino)-benzamide	469
170	5-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-(3-methyl-benzyl)-	473
	benzamide
171	N-Cyclopropyl-5-iodo-2-(4-iodo-2-methyl-phenylamino)-	517
	benzamide
172	5-Bromo-2-(4-iodo-2-methyl-phenylamino)-N-methyl-N-phenyl-	519
	benzamide
173	N-Benzyloxy-2-(4-iodo-2-methyl-phenylamino)-5-nitro-	502
	benzamide
174	N-Cyclohexyl-5-iodo-2-(4-iodo-2-methyl-phenylamino)-	559
	benzamide
175	N-Allyl-5-iodo-2-(4-iodo-2-methyl-phenylamino)-benzamide	517
176	5-Iodo-2-(4-iodo-2-methyl-phenylamino)-N-(3-methyl-benzyl)-	581
	benzamide
177	2-(4-Iodo-2-methyl-phenylamino)-N-(3-methyl-benzyl)-5-nitro-	500
	benzamide
178	5-Iodo-2-(4-iodo-2-methyl-phenylamino)-N-methyl-N-phenyl-	567
	benzamide
179	N-Cyclohexyl-5-fluoro-2-(4-iodo-2-methyl-phenylamino)-	451
	benzamide
180	5-Chloro-N-cyclohexyl-2-(4-iodo-2-methyl-phenylamino)-	467
	benzamide
181	5-Bromo-2-(4-iodo-2-methyl-phenylamino)-N-(3-methyl-benzyl)-	533
	benzamide
182	5-Bromo-N-cyclohexyl-2-(4-iodo-2-methyl-phenylamino)-	511
	benzamide
183	5-Chloro-2-(4-iodo-2-methyl-phenylamino)-N-(3-methyl-benzyl)-	489
	benzamide
184	N-Cyclohexyl-2-(4-iodo-2-methyl-phenylamino)-5-nitro-	478
	benzamide
185	N-Benzyloxy-5-bromo-2-(4-iodo-2-methyl-phenylamino)-	538
	benzamine
186	N-Benzyloxy-5-fluoro-2-(4-iodo-2-methyl-phenylamino)-	477
	benzamide
187	5-Chloro-N-(2-hydroxy-ethyl)-2-(4-iodo-2-methyl-phenylamino)-	431
	benzamide
188	5-Bromo-N-(2-hydroxy-ethyl)-2-(4-iodo-2-methyl-phenylamino)-	475
	benzamide
189	2-(4-Iodo-2-methyl-phenylamino)-N-methyl-5-nitro-N-phenyl-	488
	benzamide
190	5-Chloro-2-(4-iodo-2-methyl-phenylamino)-N-methyl-N-phenyl-	477
	benzamide
191	N-(2-Hydroxy-ethyl)-5-iodo-2-(4-iodo-2-methyl-phenylamino)-	523
	benzamide
192	5-Chloro-N-cyclopropyl-2-(4-iodo-2-methyl-phenylamino)-	425
	benzamide
193	N-Allyl-5-chloro-2-(4-iodo-2-methyl-phenylamino)-benzamide	427
194	5-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-methyl-N-phenyl-	461
	benzamide
195	N-(2-Hydroxy-ethyl)-2-(4-iodo-2-methyl-phenylamino)-5-nitro-	442
	benzamide
196	5-Fluoro-N-(2-hydroxy-ethyl)-2-(4-iodo-2-methyl-phenylamino)-	415
	benzamide
197	5-Bromo-N-cyclopropyl-2-(4-iodo-2-methyl-phenylamino)-	472
	benzamide
198	N-Cyclopropyl-5-fluoro-2-(4-iodo-2-methyl-phenylamino)-	411
	benzamide
199	5-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-(4-sulfamoyl-	540
	benzyl)-benzamide
200	N-Cyclopropyl-2-(4-iodo-2-methyl-phenylamino)-5-nitro-	438
	benzamide
201	N-Allyl-5-fluoro-2-(4-iodo-2-methyl-phenylamino)-benzamide	411
202	N-Benzyloxy-5-iodo-2-(4-iodo-2-methyl-phenylamino)-	585
	benzamide
203	N-Allyl-5-bromo-2-(4-iodo-2-methyl-phenylamino)-benzamide	472
204	5-Bromo-2-(4-iodo-2-methyl-phenylamino)-N-(4-sulfamoyl-	601
	benzyl)-benzamide
205	5-Bromo-2-(4-iodo-2-methyl-phenylamino)-N-methyl-N-phenyl-	522
	benzamide
206	N-Allyl-2-(4-iodo-2-methyl-phenylamino)-5-nitro-benzamide	438
*M + H

EXAMPLE 207

Preparation of [4-Chloro-2-(1H-tetrazol-5-yl)-(4-iodo-2-methyl-phenyl)-amine

Step a: Preparation of 5-chloro-2-fluoro-benzaldehyde

[0372] To a solution of 1-chloro-4-fluorobenzne (13.06 g, 0.1 mol) in THF (180 mL), at −78° C., LDA (2M solution in THF, 50 mL, 0.1 mol) was added drop wise. After stirring at −78° C. for 1.5 hours, DMF (8 mL) was added to the reaction mixture and allowed to warm up to room temperature overnight. The reaction mixture was partitioned between water and Et2O. The Et2O layer was dried (MgSO4) and the solvent removed in vacuum to give 14.95 g (94%) yield of crude dehyde: 1H NMR (CDCl3): δ 10.3 (s, —C(═O)H).

Step b: Preparation of 5-chloro-2-fluoro-benzaldehyde oxime

[0373] A solution of 5-chloro-2-fluoro-benzaldehyde (10 g, 0.0631 mol), hydroxylamine hydrochloride (6.57 g, 0.0946 mol) and pyridine (8.3 mL, 0.1010 mol) in EtOH (100 mL) was heated at 75° C. (oil bath temperature) for 1 hour and the solvent removed under vacuum to give an oil. The oil was partitioned between water and CH2Cl2. The CH2Cl2 layer was dried (MgSO4) and the solvent removed under vacuum to give crude aldoxime as a solid. The solid was purified by medium pressure liquid chromatography on silica. Elution with CH2Cl2 gave 4.87 g (28%) of the aldoxime as white solid: mp 95-97° C.;

[0374] Analysis calculated for C7H5NOFCl: C, 48.44; H, 2.90; N, 8.07. Found: C, 48.55; H, 2.69, N, 7.90.

Step c: Preparation of 5-chloro-2-fluoro-benzonirile

[0375] A solution of the 5-chloro-2-fluoro-benzaldehyde oxime (3.15 g, 0.0182 mol) in acetic anhydride (150 mL) was refluxed for 16 hours. The reaction mixture was cooled to room temperature and poured into saturated aqueous NaHCO3 (200 mL) solution. The mixture was extracted with Et2O. The Et2O layer was dried (K2CO3) and the solvent removed to give the product as an oily solid. The product was used without further purification in the next step.

Step d: Preparation of 5-(5-chloro-2-fluoro-phenyl)-1H-tetrazole

[0376] A mixture of 5-chloro-2-fluoro-benzonitrile (2.84 g, 0.01823 mol), butanol (15 mL), sodium azide (1.543 g, 0.0237 mol), acetic acid (1.36 mL, 0.0237 mol) was refluxed for 24 hours. The reaction mixture was cooled to room temperature, additional 1.543 g sodium azide added, and the reaction mixture refluxed for additional 24 hours. After cooling to room temperature, Et2O (100 mL) and 10% aqueous NaOH (200 mL) were added sequentially. The mixture was vigorously stirred. The aqueous layer was separated, cooled with ice-methanol bath (−15° C.) and acidified to pH 1 with conc. HCl. A gray solid precipitated. The solid was dried in vacuum at 50° C. to give 1.76 g (49%) of 5-(5-chloro-2-fluoro-phenyl)-1H-tetrazole: mp partial melt at 110° C., complete melting at 124° C.);

[0377] 1 H (400 Mz, CDCl3): δ 8.19-8.08 (m, 1H), 7.77-7.71 (m, 1H), 7.61-7.52 (m, 1H); 13C (100 Mz, CDCl3): δ 159.00, 156.49, 140.88, 133.02, 132.93, 130.73, 129.23, 129.21, 129.08, 126.05, 118.96, 118.73, 114.50; MS (CI) M+1=199 (100), M=198 (6).

Step e: Preparation of [4-Chloro-2-(1H-tetrazol-5-yl)-(4-iodo-2-methyl-phenyl)-amine

[0378] To a solution of 2-methyl-4-iodoaniline (3.52 g, 0.0151 mol) in THF (25 mL) at −78° C., LDA (2 molar solution in THF, 11.33 mL, 0.02267 mol) was added dropwise. After stirring for 0.5 hours, a solution of 1-(tetrazol-5-yl)-2-fluoro-5-chlorobenzene (1.5 g, 0.00756 mol) in THF (15 mL) was added dropwise. The reaction was stirred for 16 hours as it warmed up to room temperature. The reaction mixture was quenched with aqueous conc. NH4Cl solution and extracted with CH2Cl2. The organic layer was dried (MgSO4) and the solvent removed giving a crude product as an oil. The oil with CH2Cl2→CH2Cl2:MeOH (9.7:0.3) gave 1.5 g (48%) of the desired product:

[0379] mp 205-208° C.; 1H (400 Mz, DMSO): δ 9.13 (s, 1H), 8.00-7.99 (s, 1H), 7.69 (s, 1H), 7.55-7.52 (m, 1H), 7.43-7.40 (m, 1H), 7.12-7.05 (m, 1H), 2.24 (s, 3H); 13C (100 Mz, CDCl3): δ 141.87, 139.28, 138.88, 135.47, 133.71, 131.65, 128.15, 123.69, 121.94, 116.68, 87.79, 17.22; MS (CI) M+2=413 (44), M+1=412 (85), M=411 (100). Analysis calculated for C14H11N5ClI.0.5H2O: C, 39.97; H, 2.87; N, 16.65. Found: C, 38.87, H, 2.77; N, 16.47.

[0380] The following tetrazole substituted phenylamines were prepared by following the general procedure of Example 207.

EXAMPLE 208

(4-iodo-2-methyl-phenyl)-[2-(1H-tetrazol-5-yl)-phenyl]amine, mp 231° C. (dec)

EXAMPLE 209

[4-nitro-2-(1H-tetrazol-5-yl)-(4-iodo-2-methyl-phenyl)-amine, mp 205-208° C.

[0381] The 4-bromo and 4-iodo phenylamino benzhydroxamic acid derivatives of Formula II can be prepared from commercially available starting materials utilizing synthetic methodologies well-known to those skilled in organic chemistry. A typical synthesis is carried out by reacting a 4-bromo or 4-iodo aniline with a benzoic acid having a leaving group at the 2-position to give a phenylamino benzoic acid, and then reacting the benzoic acid phenylamino derivative with a hydroxylamine derivative (Scheme 3), where L is a leaving group, for example halo such as fluoro, chloro, bromo or iodo, or an activated hydroxy group such as a diethylphosphate, trimethylsilyloxy, p-nitrophenoxy, or phenylsulfonoxy.

[0382] The reaction of aniline and the benzoic acid derivative generally is accomplished by mixing the benzoic acid with an equimolar quantity or excess of the aniline in an unreactive organic solvent such as tetrahydrofuran, or toluene, in the presence of a base such as lithium diisopropylamide, n-butyl lithium, sodium hydride, and sodium amide. The reaction generally is carried out at a temperature of about −78° C. to about 25° C., and normally is complete within about 2 hours to about 4 days. The product can be isolated by removing the solvent, for example by evaporation under reduced pressure, and further purified, if desired, by standard methods such as chromatography, crystallization, or distillation. 6

[0383] The phenylamino benzoic acid next is reacted with a hydroxylamine derivative HNR6aOR7a in the presence of a peptide coupling reagent. Hydroxylamine derivatives that can be employed include methoxylamine, N-ethyl-isopropoxy amine, and tetrahydro-oxazine. Typical coupling reagents include 2-ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline (EEDQ), 1,3-dicyclohexylcarbodiimide (DCC), bromo-tris(pyrrolidino)-phosphonium hexafluorophosphate (PyBrOP) and (benzotriazolyloxy)tripyrrolidino phosphonium hexafluorophosphate (PyBOP). The phenylamino benzoic acid and hydroxylamino derivative normally are mixed in approximately equimolar quantities in an unreactive organic solvent such as dichloromethane, tetrahydrofuran, chloroform, or xylene, and an equimolar quantity of the coupling reagent is added. A base such as triethylamine or diisopropylethylamine can be added to act as an acid scavenger if desired. The coupling reaction generally is complete after about 10 minutes to 2 hours, and the product is readily isolated by removing the reaction solvent, for instance by evaporation under reduced pressure, and purifying the product by standard methods such as chromatography or crystallizations from solvents such as acetone, diethyl ether, or ethanol. An alternative method for making the invention compounds involves first converting a benzoic acid to a hydroxamic acid derivative, and then reacting the hydroxamic acid derivative with an aniline. This synthetic sequence is depicted in Scheme 4, where L is a leaving group. The general reaction conditions for both of the steps in Scheme 4 are the same as those described above for Scheme 3. 7

[0384] Yet another method for making invention compounds comprises reacting a phenylamino benzhydroxamic acid with an ester forming group as depicted in Scheme 5, where L is a leaving group such as halo, and a base is triethylamine or diisopropylamine. 8

[0385] The synthesis of compounds of Formula (II) is further illustrated by the following detailed examples.

EXAMPLE 1a

4-Fluoro-N-hydroxy-2-(4-iodo-2-methyl-phenylamino)-benzamide

(a) Preparation of 4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-benzoic acid

[0386] To a stirred solution containing 3.16 g (0.0133 mol) of 2-amino-5-iodotoluene in 5 mL of tetrahydrofuran at −78° C. was added 10 mL (0.020 mol) of a 2.0 M lithium diisopropylamide in tetrahydrofuran/heptane/ethylbenzene (Aldrich) solution. The resulting green suspension was stirred vigorously for 15 minutes, after which time a solution of 1.00 g (0.00632 mol) of 2,4-difluorobenzoic acid in 10 mL of tetrahydrofuran was added. The reaction temperature was allowed to increase slowly to room temperature, at which temperature the mixture was stirred for 2 days. The reaction mixture was concentrated by evaporation of the solvent under reduced pressure. Aqueous HCl (10%) was added to the concentrate, and the solution was extracted with dichloromethane. The organic phase was dried (MgSO4) and then concentrated over a steambath to low volume (10 mL) and cooled to room temperature. The off-white fibers which formed were collected by vacuum filtration, rinsed with hexane, and dried in a vacuum-oven (76° C.; ca. 10 mm of Hg) to afford 1.10 g (47%) of the desired material; mp 224-229.5° C.;

[0387] 1 H NMR (400 MHz, DMSO): δ 9.72 (s, 1H), 7.97 (dd, 1H, J=7.0, 8.7 Hz), 7.70 (d, 1H, J=1.5 Hz), 7.57 (dd, 1H, J=8.4, 1.9 Hz), 7.17 (d, 1H, J=8.2 Hz), 6.61-6.53 (m, 2H), 2.18 (s, 3H); 13C NMR (100 MHz, DMSO): δ 169.87, 166.36 (d, JC—F=249.4 Hz), 150.11 (d, JC—F=11.4 Hz), 139.83, 138.49, 136.07, 135.26 (d, JC—F=1.5 Hz), 135.07, 125.60, 109.32, 104.98 (d, JC—F=21.1 Hz), 99.54 (d, JC—F=26.0 Hz), 89.43, 17.52; 19F NMR (376 MHz, DMSO): δ −104.00 to −104.07 (m); IR (KBr) 1670 (C═O stretch)cm−1; MS (CI) M+1=372. Analysis calculated for C14H11FINO2: C, 45.31; H, 2.99; N, 3.77. Found: C, 45.21; H, 2.77; N, 3.64.

(b) Preparation of 4-Fluoro-N-hydroxy-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0388] To a stirred solution of 4-fluoro-2-(4-iodo-2-methyl-phenylamino)-benzoic acid (0.6495 g, 0.001750 mol), O-(tetrahydro-2H-pyran-2-yl)-hydroxylamine (0.2590 g, 0.002211 mol), and diisopropylethylamine (0.40 mL, 0.0023 mol) in 31 mL of an equivolume tetrahydrofuran-dichloromethane solution was added 1.18 g (0.00227 mol) of solid PyBOP ([benzotriazolyloxy]tripyrrolidino phosphonium hexafluorophosphate, Advanced ChemTech) directly. The reaction mixture was stirred for 30 minutes after which time it was concentrated in vacuo. The brown oil was treated with 10% aqueous hydrochloric acid. The suspension was extracted with ether. The organic extraction was washed with 10% sodium hydroxide followed by another 10% hydrochloric acid wash, was dried (MgSO4) and concentrated in vacuo to afford 1.0 g of a light-brown foam. This intermediate was dissolved in 25 mL of ethanolic hydrogen chloride, and the solution was allowed to stand at room temperature for 15 minutes. The reaction mixture was concentrated in vacuo to a brown oil that was purified by flash silica chromatography. Elution with a gradient (100% dichloromethane to 0.6% methanol in dichloromethane) afforded 0.2284 g of a light-brown viscous oil. Scratching with pentane-hexanes and drying under high vacuum afforded 0.1541 g (23%) of an off-white foam; mp 61-75° C.;

[0389] 1 H NMR (400 MHz, DMSO): δ 11.34 (s, 1H), 9.68 (s, 1H), 9.18 (s, 1H), 7.65 (d, 1H, J=1.5 Hz), 7.58 (dd, 1H, J=8.7, 6.8 Hz), 7.52 (dd, 1H, J=8.4, 1.9 Hz), 7.15 (d, 1H, J=8.4 Hz), 6.74 (dd, 1H, J=11.8, 2.4 Hz), 6.62 (ddd, 1H, J=8.4, 8.4, 2.7 Hz), 2.18 (s, 3H); 13C NMR (100 MHz, DMSO): δ 165.91, 164.36 (d, JC—F=247.1 Hz), 146.78, 139.18, 138.77, 135.43, 132.64, 130.60 (d, JC—F=11.5 Hz), 122.23, 112.52, 104.72 (d, J=22.1 Hz), 100.45 (d, JC—F=25.2 Hz), 86.77, 17.03; 19F NMR (376 MHz, DMSO): δ −107.20 to −107.27 (m); IR (KBr) 3307 (broad, O—H stretch), 1636 (C═O stretch) cm−1; MS (CI) M+1=387. Analysis calculated for C14H12FIN2O2: C, 43.54; H, 3.13; N, 7.25. Found: C, 43.62; H, 3.24; N, 6.98.

EXAMPLE 2a

5-Bromo-3,4-difluoro-N-hydroxy-2-(4-iodo-2-methyl-phenylamino)-benzamide

(a) Preparation of 5-Bromo-2,3,4-trifluorobenzoic acid

[0390] To a stirred solution comprised of 1-bromo-2,3,4-trifluorobenzene (Aldrich, 99%; 5.30 g, 0.0249 mol) in 95 mL of anhydrous tetrahydrofuran cooled to −78° C. was slowly added 12.5 mL of 2.0 M lithium diisopropylamide in heptane/tetrahydrofuran/ethylbenzene solution (Aldrich). The mixture was stirred for 1 hour and transferred by canula into 700 mL of a stirred saturated ethereal carbon dioxide solution cooled to −78° C. The cold bath was removed, and the reaction mixture was stirred for 18 hours at ambient temperature. Dilute (10%) aqueous hydrochloric acid (ca. 500 mL) was poured into the reaction mixture, and the mixture was subsequently concentrated on a rotary evaporator to a crude solid. The solid product was partitioned between diethyl ether (150 mL) and aq. HCl (330 mL, pH 0). The aqueous phase was extracted with a second portion (100 mL) of diethyl ether, and the combined ethereal extracts were washed with 5% aqueous sodium hydroxide (200 mL) and water (100 mL, pH 12). These combined alkaline aqueous extractions were acidified to pH 0 with concentrated aqueous hydrochloric acid. The resulting suspension was extracted with ether (2×200 mL). The combined organic extracts were dried (MgSO4), concentrated in vacuo, and subjected to high vacuum until constant mass was achieved to afford 5.60 g (88% yield) of an off-white powder; mp 139-142.5° C.;

[0391] 1 H NMR (400 MHz, DMSO): δ 13.97 (broad s, 1H, 8.00-7.96 (m, 1H); 13C NMR (100 MHz, DMSO): δ 162.96, 129.34, 118.47, 104.54 (d, JC—F=22.9 Hz); 19F NMR (376 MHz, DMSO): δ −120.20 to −120.31 (m), −131.75 to −131.86 (m), −154.95 to −155.07 (m); IR (KBr) 1696 (C═O stretch)cm−1; MS (CI) M+1=255. Analysis calculated for C74H21BrF3O2: C, 32.97; H, 0.79; N, 0.00; Br, 31.34; F, 22.35. Found: C, 33.18; H, 0.64; N, 0.01; Br, 30.14; F, 22.75.

(b) Preparation of 5-Bromo-3,4-difluoro-2-(4-iodo-2-methyl-phenylamino)-benzoic acid

[0392] To a stirred solution comprised of 1.88 g (0.00791 mol) of 2-amino-5-iodotoluene in 10 mL of tetrahydrofuran at −78° C. was added 6 mL (0.012 mol) of a 2.0 M lithium diisopropylamide in tetrahydrofuran/heptane/ethylbenzene (Aldrich) solution. The resulting green suspension was stirred vigorously for 10 minutes, after which time a solution of 1.00 g (0.00392 mol) of 5-bromo-2,3,4-trifluorobenzoic acid in 15 mL of tetrahydrofuran was added. The cold bath was subsequently removed, and the reaction mixture stirred for 18 hours. The mixture was concentrated, and the concentrate was treated with 100 mL of dilute (10%) aqueous hydrochloric acid. The resulting suspension was extracted with ether (2×150 mL), and the combined organic extractions were dried (MgSO4) and concentrated in vacuo to give an orange solid. The solid was triturated with boiling dichloromethane, cooled to ambient temperature, and collected by filtration. The solid was rinsed with dichloromethane, and dried in the vacuum-oven (80° C.) to afford 1.39 g (76%) of a yellow-green powder; mp 259.5-262° C.;

[0393] 1 H NMR (400 MHz, DMSO): δ 9.03 (s, 1H), 7.99 (dd, 1H, J=7.5, 1.9 Hz), 7.57 (dd, 1H, J=1.5 Hz), 7.42 (dd, 1H, J=8.4, 1.9 Hz), 6.70 (dd, 1H, J=8.4, 6.0 Hz), 2.24 (s, 3H); 19F NMR (376 MHz, DMSO): δ −123.40 to −123.47 (m); −139.00 to −139.14 (m); IR (KBr) 1667 (C═O stretch)cm−1; MS (CI) M+1=469. Analysis calculated for C14H9BrF2INO2: C, 35.93; H, 1.94; N, 2.99; Br, 17.07; F, 8.12; I, 27.11. Found: C, 36.15; H, 1.91; N, 2.70; Br, 16.40; F, 8.46; I, 26.05.

(c) Preparation of 5-Bromo-3,4-difluoro-N-hydroxy-2-(4-iodo-2-methyl-phenylamino)-benzamide

[0394] To a stirred solution comprised of 5-bromo-3,4-difluoro-2-(4-iodo-2-methyl-phenylamino)-benzoic acid (0.51 g, 0.0011 mol), O-(tetrahydro-2H-pyran-2-yl)-hydroxylamine (0.15 g, 0.0013 mol), and diisopropylethylamine (0.25 mL, 0.0014 mol) in 20 mL of an equivolume tetrahydrofuran-dichloromethane solution was added 0.6794 g (0.001306 mol) of solid PyBOP (Advanced ChemTech) directly. The reaction mixture was stirred at 24° C. for 10 minutes, and then was concentrated to dryness in vacuo. The concentrate was suspended in 100 mL of 10% aqueous hydrochloric acid. The suspension was extracted with 125 mL of diethyl ether. The ether layer was separated, washed with 75 mL of 10% aqueous sodium hydroxide, and then with 100 mL of dilute acid. The ether solution was dried (MgSO4) and concentrated in vacuo to afford 0.62 g (100%) of an off-white foam. The foam was dissolved in ca. 15 mL of methanolic hydrogen chloride. After 5 minutes, the solution was concentrated in vacuo to an oil, and the oil was purified by flash silica chromatography. Elution with dichloromethane: dichloromethane-methanol (99:1) afforded 0.2233 g (42%) of a yellow powder. The powder was dissolved in diethyl ether and washed with dilute hydrochloric acid. The organic phase was dried (MgSO4) and concentrated in vacuo to afford 0.200 g of a foam. This product was triturated with pentane to afford 0.1525 g of a powder that was repurified by flash silica chromatography. Elution with dichloromethane afforded 0.0783 g (15%) of an analytically pure title compound, mp 80-90° C.;

[0395] 1 H NMR (400 MHz, DMSO): δ 11.53 (s, 1H), 9.38 (s, 1H), 8.82 (s, 1H), 7.70 (dd, 1H, J=7.0, 1.9 Hz), 7.53 (s, 1H), 7.37 (dd, 1H, J=8.4, 1.9 Hz), 6.55 (dd, 1H, J=8.2, 6.5 Hz), 2.22 (s, 3H); 19F NMR (376 MHz, DMSO): δ −126.24 to −126.29 (m), −137.71 to −137.77 (m); IR (KBr) 3346 (broad, O—H stretch), 1651 (C═O stretch)cm−1; MS (CI) M+1=484. Analysis calculated for C14H10BrF2IN2O2: C, 34.81; H, 2.09; N, 5.80. Found: C, 34.53; H, 1.73; N, 5.52.

[0396] Examples 3a to 12a in the table below were prepared by the general procedure of Examples 1a and 2a.

EXAMPLES 13a-77a

[0397] Examples 13a to 77a were prepared utilizing combinatorial synthetic methodology by reacting appropriately substituted phenylamino benzoic acids (e.g., as shown in Scheme 1) and hydroxylamines (e.g., (NHR6a)—O—R7a). A general method is given below:

[0398] To a 0.8-mL autosampler vial in a metal block was added 40 μL of a 0.5 M solution of the acid in DMF and 40 μL of the hydroxylamine (2 M solution in Hunig's base and 1 M in amine in DMF). A 0.5 M solution of PyBrOP was freshly prepared, and 50 μL were added to the autosampler vial. The reaction was allowed to stand for 24 hours.

[0399] The reaction mixture was transferred to a 2-dram vial and diluted with 2 mL of ethyl acetate. The organic layer was washed with 3 mL of distilled water and the water layer washed again with 2 mL of ethyl acetate. The combined organic layers were allowed to evaporate to dryness in an open fume hood.

[0400] The residue was taken up in 2 mL of 50% acetonitrile in water and injected on a semi-prep reversed phase column (10 mm×25 cm, 5 μM spherical silica, pore Size 115 A derivatized with C-18, the sample was eluted at 4.7 mL/min with a linear ramp to 100% acetonitrile over 8.5 minutes. Elution with 100% acetonitrile continued for 8 minutes.) Fractions were collected by monitoring at 214 nM. The desired fractions were evaporated using a Zymark Turbovap. The product was dissolved in chloroform and transferred to a preweighed vial, evaporated, and weighed again to determine the yield. The structure was confirmed by mass spectroscopy.

EXAMPLES 3a-77a

[0401]

Example		Melting	MS
No.	Compound	Point (° C.)	(M − H+)
3a	2-(4-bromo-2-methyl-phenylamino)-4-fluoro-N-	56-75	523
	hydroxy-benzamide	dec
4a	5-Chloro-N-hydroxy-2-(4-iodo-2-methyl-	65
	phenylamino)-benzamide	dec
5a	5-Chloro-N-hydroxy-2-(4-iodo-2-methyl-	62-67
	phenylamino)-N-methyl-benzamide
6a	5-Chloro-2-(4-iodo-2-methyl-phenylamino)-N-	105-108
	(terahydropyran-2-yloxy)benzamide
7a	5-Chloro-2-(4-iodo-2-methyl-phenylamino)-N-	64-68
	methoxybenzamide
8a	4-Fluoro-N-hydroxy-2-(4-fluoro-2-methyl-	119-135
	phenylamino)-benzamide
9a	4-Fluoro-N-hydroxy-2-(2-methyl phenylamino)-	101-103
	benzamide
10a	4-Fluoro-2-(4-fluor-2-methyl-phenylamino)-N-	142-146
	(terahydropyran-2-yloxy)benzamide
11a	4-Fluoro-N-hydroxy-2-(4-cluoro-2-methyl-	133.5-135
	phenylamino)-benzamide
12a	4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-	107-109.5
	phenylmethoxy-benzamide
13a	4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-		399
	methoxy-benzamide
14a	3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-		417
	N-methoxy-benzamide
15a	2-(4-Bromo-2-methyl-phenylamino)-		369
	3,4-difluoro-N-methoxy-benzamide
16a	2-(4-Bromo-2-methyl-phenylamino)-N-ethoxy-		342*
	3,4-difluoro-benzamide		(M − EtO)
17a	5-Bromo-N-ethoxy-3,4-difluoro-2-(4-iodo-		509
	2-methyl-phenylamino)-benzamide
18a	3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-		445
	N-isopropoxy-benzamide
19a	2-(4-Bromo-2-methyl-phenylamino)-		397
	3,4-difluoro-N-isopropoxy-benzamide
20a	4-Fluoro-N-(furan-3-ylmethoxy)-2-(4-iodo-		465
	2-methyl-phenylamino)-benzamide
21a	3,4-Difluoro-N-(furan-3-ylmethoxy)-2-(4-iodo-		483
	2-methyl-phenyIamino)-benzamide
22a	2-(4-Bromo-2-methyl-phenylamino)-		435
	3,4-difluoro-N-(furan-3-ylmethoxy)-benzamide
23a	5-Bromo-3,4-difluoro-N-(furan-3-ylmethoxy)-		561
	2-(4-iodo-2-methyl-phenylamino)-benzamide
24a	5-Bromo-N-(but-2-enyloxy)-3,4-difluoro-		536
	2-(4-iodo-2-methyl-phenylamino)-benzamide
25a	4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-		423
	(prop-2-ynyloxy)-benzamide
26a	3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-		441
	N-(prop-2-ynyloxy)-benzamide
27a	3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-		455
	N-(1-methyl-prop-2-ynyloxy)-benzamide
28a	2-(4-Bromo-2-methyl-phenylamino)-		407
	3,4-difluoro-N-(1-methyl-prop-2-ynyloxy)-
	benzamide
29a	N-(But-3-ynyloxy)-3,4-difluoro-2-(4-iodo-		455
	2-methyl-phenylamino)-benzamide
30a	2-(4-Bromo-2-methyl-phenylamino)-N-(but-		407
	3-ynyloxy)-3,4-difluoro-benzamide
31a	5-Bromo-N-(but-3-ynyloxy)-3,4-difluoro-		533
	2-(4-iodo-2-methyl-phenylamino)-benzamide
32a	3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-		517
	N-(3-phenyl-prop-2-ynyloxy)-benzamide
33a	3,4-Difluoro-2-(4-bromo-2-methyl-		469
	phenylamino)-N-(3-phenyl-prop-2-ynyloxy)-
	benzamide
34a	3,4-Difluoro-N-[3-(3-fluoro-phenyl)-prop-		535
	2-ynyloxy]-2-(4-iodo-2-methyl-phenylamino)-
	benzamide
35a	2-(4-Bromo-2-methyl-phenylamino)-		487
	3,4-difluoro-N-[3-(3-fluoro-phenyl)-prop-
	2-ynyloxy]-benzamide
36a	3,4-Difluoro-N-[3-(2-fluoro-phenyl)-prop-		535
	2-ynyloxy]-2-(4-iodo-2-methyl-phenylamino)-
	benzamide
37a	5-Bromo-3,4-difluoro-N-[3-(2-fluoro-phenyl)-		613
	prop-2-ynyloxy]-2-(4-iodo-2-methyl-
	phenylamino)-benzamide
38a	3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-		557*
	N-(3-methyl-5-phenyl-pent-2-en-4-ynyloxy)-		*(M + H)
	benzamide
39a	2-(4-Bromo-2-methyl-phenylamino)-		510
	3,4-difluoro-N-(3-methyl-5-phenyl-pent-2-en-
	4-ynyloxy)-benzamide
40a	N-Ethoxy-3,4-difluoro-2-(4-iodo-2-methyl-		431
	phenylamino)-benzamide
41a	2-(4-Bromo-2-methyl-phenylamino)-N-ethoxy-		383
	3,4-difluoro-benzamide
42a	4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-		427
	propoxy-benzamide
43a	3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-		445
	N-propoxy-benzamide
44a	2-(4-Bromo-2-methyl-phenylamino)-		397
	3,4-difluoro-N-propoxy-benzamide
45a	5-Bromo-3,4-difluoro-2-(4-iodo-2-methyl-		523
	phenylamino)-N-propoxy-benzamide
46a	4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-		427
	isopropoxy-benzamide
47a	3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-		445
	N-isopropoxy-benzamide
48a	2-(4-Bromo-2-methyl-phenylamino)-		397
	3,4-difluoro-N-isopropoxy-benzamide
49a	5-Bromo-3,4-difluoro-2-(4-iodo-2-methyl-		523
	phenylamino)-N-isopropoxy-benzamide
50a	N-Cyclobutyloxy-3,4-difluoro-2-(4-iodo-		457
	2-methyl-phenylamino)-benzamide
51a	2-(4-Bromo-2-methyl-phenylamino)-N-		409
	cyclobutyloxy-3,4-difluoro-benzamide
52a	N-Cyclopentyloxy-4-fluoro-2-(4-iodo-2-methyl-		453
	phenylamino)-benzamide
53a	N-Cyclopentyloxy-3,4-difluoro-2-(4-iodo-		471
	2-methyl-phenylamino)-benzamide
54a	2-(4-Bromo-2-methyl-phenylamino)-N-		423
	cyclopentyloxy-3,4-difluoro-benzamide
55a	N-Cyclopropylmethoxy-4-fluoro-2-(4-iodo-		439
	2-methyl-phenylamino)-benzamide
56a	N-Cyclopropylmethoxy-3,4-difluoro-2-(4-iodo-		457
	2-methyl-phenylamino)-benzamide
57a	2-(4-Bromo-2-methyl-phenylamino)-N-		409
	cyclopropylmethoxy-3,4-difluoro-benzamide
58a	5-Bromo-N-cyclopropylmethoxy-3,4-difluoro-		435
	2-(4-iodo-2-methyl-phenylamino)
59a	4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-		505
	(2-phenoxy-ethoxy)-benzamide
60a	3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-		523
	N-(2-phenoxy-ethoxy)-benzamide
61a	2-(4-Bromo-2-methyl-phenylamino)-		475
	3,4-difluoro-N-(2-phenoxy-ethoxy)-benzamide
62a	4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-		481
	(thiophen-2-ylmethoxy)-benzamide
63a	3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-		499
	N-(thiophen-2-ylmethoxy)-benzamide
64a	2-(4-Bromo-2-methyl-phenylamino)-		451
	3,4-difluoro-N-(thiophen-2-ylmethoxy)-
	benzamide
65a	4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-		439
	(2-methyl-allyloxy)-benzamide
66a	3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-		457
	N-(2-methyl-allyloxy)-benzamide
67a	2-(4-Bromo-2-methyl-phenylamino)-		410
	3,4-difluoro-N-(2-methyl-allyloxy)-benzamide
68a	N-(But-2-enyloxy)-4-fluoro-2-(4-iodo-2-methyl-		439
	phenylamino)-benzamide
69a	N-(But-2-enyloxy)-3,4-difluoro-2-(4-iodo-		457
	2-methyl-phenylamino)-benzamide
70a	2-(4-Bromo-2-methyl-phenylarnino)-N-(but-		410
	2-enyloxy)-3,4-difluoro-benzamide
71a	3,4-Difluoro-2-(4-iodo-2-methyl-phenylamino)-		441
	N-(prop-2-ynyloxy)-benzamide
72a	N-(But-3-ynyloxy)-3,4-difluoro-2-(4-iodo-		455
	2-methyl-phenylamino)-benzamide
73a	2-(4-Bromo-2-methyl-phenylamino)-N-		449
	(4,4-dimethyl-pent-2-ynyloxy)-3,4-difluoro-
	benzamide
74a	N-(But-2-enyloxy)-3,4-difluoro-2-(4-iodo-		457
	2-methyl-phenylamino)-benzamide
75a	2-(4-Bromo-2-methyl-phenylamino)-N-(but-		410
	2-enyloxy)-3,4-difluoro-benzamide
76a	N-(3-tert-butyl-propyn-2-yl)oxy-4-fluoro-		479
	2-(4-iodo-2-methyl-phenylamino)-benzamide
77a	4-Fluoro-2-(4-iodo-2-methyl-phenylamino)-N-		577
	phenylmethoxy-benzamide

[0402]

PHYSICAL DATA FOR SELECTED COMPOUNDS
PD 0171984
mp 80-90° C.
PD 0184161
mp 174-175° C.
PD 0203311
mp 141-144° C.
PD 0297189
mp 167-169° C.
1                  H—NMR (400 MHz; DMSO) δ 11.70 (s, 1H), 8.59 (s, 1H),
7.55 (s, 1H), 7.43 (d, 1H, J=6.5 Hz), 7.27 (d, 1H,
J=8.7 Hz), 6.46 (m, 1H), 3.42 (d, 2H, J=7.0 Hz),
0.84 (m, 1H), 0.27 (m, 2H), 0.00 (m, 2H)
PD 0297190
mp 125.5-133° C.
1                  H—NMR (400 MHz; DMSO) δ 11.48 (s, 1H), 8.32 (s, 1H),
7.34 (d, 1H, J=7.5 Hz), 7.28 (d, 2H, J=8.2 Hz),
6.48 (d, 2H, J=7.7 Hz), 3.32 (d, 2H, J=6.8 Hz),
0.81 (m, 1H), 0.28 (m, 2H), 0.00 (m, 2H)
PD 0296771
mp 266.7-268.9° C.
1                  H—NMR (400 MHz; DMSO) δ 13.85 (broad s, 1H), 8.99
(s, 1H), 7.87 (dd, 1H, J=7.9, 2.1 Hz), 7.55 (d,
2H, J=8.6 Hz), 6.82 (dd, 2H, J=8.7, 2.8 Hz)
PD 0296770
mp 293.2-296.3° C.
1                  H—NMR (400 MHz; DMSO) δ 14.05 (broad s, 1H), 9.21
(s, 1H), 7.93 (dd, 1H, J=7.8, 2.2 Hz), 7.82 (d, 1H,
J=1.9 Hz), 7.54 (dd, 1H, J=8.6, 1.9 Hz), 6.82
(dd, 1H, J=8.6, 6.7 Hz)
PD 0296767
mp 249-251° C.
1                  H—NMR (400 MHz; DMSO) δ 13.99 (broad s, 1H), 9.01
(s, 1H), 7.90 (dd, 1H, J=7.9, 2.3 Hz), 7.58 (d, 1H,
J=1.6 Hz), 7.42 (dd, 1H, J=8.4, 1.9 Hz), 6.69
(dd, 1H, J=8.4, 6.0 Hz), 2.24 (s, 3H)
PD298127
mp 127-135° C.
5-chloro-N-cyclopropyl methoxy-3,4-difluoro-2-[4-iodo-2-methyl
phenylamino]benzamide
Proton NMR (440 MHz; DMSO) δ 11.64 (s, 1H), 8.28
(s, 1H), 7.38 (dd, 1H, J=7.6, 1.7 Hz), 7.31 (d, 1H,
J=1.2 Hz), 7.15 (dd, 1H, J=8.5, 1.7 Hz), 3.35
(d, 2H, J=7.3 Hz), 2.01 (s, 3H), 0.83 (m, 1H), 0.28
(m, 2H), 0.01 (m,2H)

Biological Assays

[0403] The ability of MEK inhibitors described above to prevent and treat asthma has been demonstrated in three different assays: (1) inhibition of antigen-induced interleukin-5 (IL-5) production in vitro, (2) inhibition of the passive-transfer of eosinophilic lung inflammation in vivo, and (3) inhibition of active eosinophilic lung inflammation in vivo. For each of these assays, female C57BL/6 mice obtained from the Jackson Laboratory (Bar Harbor, Me.) were given an intraperitoneal (i.p.) injection of ovalbumin (OVA, Grade V, Sigma Chemical Company, St. Louis, Mo.) adsorbed to aluminum hydroxide (10 μg OVA+9 mg aluminum hydroxide in 200 μL saline). This sensitizes OVA-specific lymphocytes for subsequent restimulation either in vivo or in vitro.

[0404] The first set of experiments was designed to determine whether the MEK inhibitors could prevent antigen-induced production of IL-5 by the OVA-primed splenocytes in vitro. IL-5 is required for the differentiation, migration, and survival of pulmonary eosinophils, which are thought to be responsible for much of the pathology associated with human asthma. In order to examine the effects of MEK inhibitors on IL-5 production, OVA-sensitized mice were sacrificed by cervical dislocation 14 days after sensitization (Day 14), the spleens were excised and disaggregated, and the erythrocytes were lysed. The splenocytes were washed and resuspended at 5×106 cells/mL in complete medium consisting of RPMI 1640 (Gibco BRL, Gaithersburg, Md.) with 10% heat-inactivated fetal calf serum (Hyclone, Logan, Utah), 55 μM 2-mercaptoethanol, 50 U/mL penicillin G, 50 μg/mL streptomycin sulfate, and 2 mM L-glutamine (Gibco BRL). The splenocytes were then cultured at 37° C. in the presence of 200 μg/mL OVA. MEK inhibitors were also added to the cultures from sterile 10 mM stock solutions (in DMSO). After 3 days, the culture medium was recovered and assayed for IL-5 by specific ELISA. The results of the analysis of IL-5 inhibition are presented in Table 1. All MEK inhibitors tested were found to potently inhibit antigen-induced IL-5 production.

TABLE 1
The Effects of MEK Inhibitors on Antigen-
Induced IL-5 Production
MEK Inhibitor IC50 (nM)
PD 184386     23
PD 171984     117
PD 170611     1,121
PD 184161     1,147
PD 177168     1,205
PD 184352     1,622
PD 098059     17,440

[0405] When OVA-sensitized spleen cells are restimulated with OVA in vitro for 3 days, as described above, the spleen cells not only produce IL-5, but also acquire the ability to induce eosinophilic lung inflammation when transferred into naïve recipient mice. The critical cell type responsible for this adoptively-transferred activity is thought to be IL-5-producing T lymphocytes. Because the results of the first set of experiments indicated that the MEK inhibitors inhibited IL-5 production by cultured splenocytes, a second set of experiments was initiated to determine whether the MEK inhibitor-treated cells were capable of transferring eosinophilic lung inflammation to naïve mice. Splenocytes from OVA restimulation cultures, with or without the addition of MEK inhibitors were harvested after 3 days of culture, washed three times, and resuspended at 1×108 cells/mL in sterile saline. Groups of five naïve (unsensitized) C57BL/c mice were injected i.p. with 200 μL of the cell suspension (2×107 cells). Three days after transfer of cells, the recipient mice were challenged with a 12-minute inhalation of an aerosol formulation of 1.5% OVA in saline (weight/volume), the mist being produced by a nebulizer (small particle generator model SPAG-2, ICN Pharmaceuticals, Costa Mesa, Calif.). Three days after aerosol challenge, the mice were anesthetized with an i.p. injection of an anesthetic mixture comprising Ketamine, acepromazine, and xylazine. The trachea of each mouse was exposed and cannulated. The lungs and upper airways were lavaged with 0.5 mL of cold (5° C.) phosphate buffered saline (PBS). The cells within a 200 μL portion of the bronchoalveolar lavage (BAL) fluid were enumerated using a Coulter counter (Model ZB 1, Coulter Electronics, Hialeah, Fla.). The remaining BAL fluid was then centrifuged at 300×g for 5 minutes, and the cells resuspended in 1 mL of Hank's balanced salt solution (HBSS, Gibco BRL), containing 0.5% fetal calf serum, and 10 mM of N-2-hydroxyethylpiperazine-N-2-ethanesulfonic acid (HEPES, Gibco BRL). The cell suspension (100 μL) was centrifuged in a cytospin (Shandon Southern Instruments, Sewickley, Pa.) and stained with Diff Quick to distinguish neutrophil, eosinophil, monocyte, and lymphocyte subsets. The number of eosinophils in the BAL fluid was determined by multiplying the percentage of eosinophils by the total cell count.

[0406] As shown in Table 2, OVA-sensitized splenocytes cultured in the absence of MEK inhibitor, when transferred to naïve recipient mice, were able to promote eosinophilic lung inflammation in response to an aerosol challenge with OVA. In contrast, splenocytes cultured in the presence of the MEK inhibitors PD 171984, PD 184352, and PD 184386 (10 μM each) did not promote eosinophilic lung inflammation (>99% inhibition). For each of the MEK inhibitors used, a 10 μM concentration was previously found to inhibit IL-5 production by over 75% (Table 1). These results suggest that the MEK inhibitors inhibit the IL-5-producing T lymphocytes that are required to support asthma-like eosinophilic lung inflammation in mice.

TABLE 2
The Effects of MEK Inhibitors on the Adoptive-Transfer
of Eosinophilic Lung Inflammation
	Treatment of Spleen
	Cell Culture	% Inhibition of
	Compound	Dose (μM)	BAL Eosinophils
	None		0
	PD 171984	10	99.82
	PD 184386	10	99.78
	PD 184352	10	99.46

[0407] The final set of experiments was designed to test whether MEK inhibitors could inhibit active OVA-induced eosinophilic lung inflammation in mice. Mice were sensitized with OVA/aluminum hydroxide on Day 0 as described above. On Day 14, the mice were challenged by aerosol with 1.5% OVA, as described above for the adoptive-transfer recipients. One group of eight sensitized mice was dosed orally with vehicle (0.5% hydroxypropylmethylcellulose/0.25% TWEEN-80). Other groups of sensitized mice (8 mice per group) were given oral doses of a MEK inhibitor. The test compound was dissolved in the vehicle, and the volume for each dosage was adjusted to 200 μL, so that each test animal received the same oral volume. In experiments reported in Table 3 and Table 4, the MEK inhibitor was administered starting on Day 13 (ie, 13 days after initial sensitization and 1 day prior to aerosol challenge), and continued daily through Day 16 (4 days total). In experiments reported in Table 5, the MEK inhibitor was administered starting on Day 7 (ie, 7 days after initial sensitization and 7 days prior to aerosol challenge), and continued daily through Day 16 (9 days total). On Day 17 of each experiment (17 days following the initial OVA challenge, and 3 days after the OVA aerosol challenge), all animals including controls were anesthetized, cannulated, and ravaged as previously described. The number of BAL eosinophils was determined as described above.

[0408] In the initial analysis of active OVA-induced lung inflammation, multiple MEK inhibitors (PD 171984, PD 177168, PD 184161, PD 184386, and PD 184352) were dosed orally for 4 days. Only one compound, PD 171984, demonstrated any inhibition of pulmonary eosinophilia (Table 3). PD 171984, along with PD 184352, were tested again at multiple doses, again dosing for only 4 days. The results in Table 4 essentially parallel those in Table 3 for these compounds; PD 171984 appears active, whereas PD 184352 does not. As reported in Table 5, increasing the oral dosing schedule from 4 days to 9 days (7 days prior to aerosol challenge, 2 days after) resulted in a degree of inhibitory activity for PD 184352 at 100 mg/kg (59.85% inhibition, p=0.11). PD 171984 continued to demonstrate statistically significant inhibitory activity under this dosing regimen.

[0409] In total, these results indicate that MEK inhibitors, when used in vitro, are potent inhibitors of IL-5 production, and completely inhibit the ability of antigen-stimulated cells to adoptively transfer asthma-like symptoms to naïve recipient mice. When used in vivo, some MEK inhibitors are more active than others. However, a less potent compound (PD 184352) was shown to inhibit the asthma-like response in mice under a more rigorous dosing regimen. Thus, the foregoing data establish that the selective MEK inhibitors are active in inhibiting a model of asthma in mice. The compounds have little or no toxic effects, and accordingly are particularly well-suited for treating and controlling asthma in children, as well as adults. The compounds will be formulated for convenient oral or parenteral administration, including by aerosol delivery, transdermal delivery, or even suppositories, and will be administered in an antiasthmatic effective dose, which is that amount that is effective to treat the particular asthma severity for which treatment is needed or otherwise desired.

TABLE 3
The Effect of MEK Inhibitors on Eosinophilic
Lung Inflammation in Mice
MEK Inhibitor	Dose (μM)	% Inhibition of BAL Eosinophilia
PD 171984	100	55.26*
PD 177168	100	−123.38
PD 184161	100	−32.53
PD 184386	100	−33.24
PD 184352	150	−5.41
*p = 0.08

[0410]

TABLE 4
Inhibition of BAL Eosinophils With 4-Day Compound Dosing
	% Inhibition of BAL
	Eosinophils by:
Dose (mg/kg)	PD 184352	PD 171984
0	0	0
10	−22.7	38.4*
30	−153.8	46.6*
100	−8.2	58.4*
*Significantly different from control (p < 0.05)

[0411]

TABLE 5
Inhibition of BAL Eosinophils With 9-Day Compound Dosing
	% Inhibition of BAL Eosinophils by:
	PD 171984
Dose (mg/kg)	PD 184352	Experiment 1	Experiment 2
0	0	0	0
10	−42.99	−13.74	50.15*
30	1.83	80.64*	37.23*
100	59.85	88.40*	54.77*
*Significantly different from control (p < 0.05)

[0412] The foregoing data establish that the selective MEK inhibitors are active in both inhibiting and controlling the asthmatic disease, for example, prior to actual challenge and following challenge. The compounds are therefore useful in the prophylaxis of asthma, and also in treating and alleviating the symptoms that accompany the disease during its active stage. The compounds have little or no toxic effects, and accordingly are particularly well-suited for treating and controlling asthma in children, as well as adults. The compounds will be formulated for convenient oral or parenteral administration, including by aerosol delivery, transdermal delivery, or even suppositories, and will be administered in an antiasthmatic effective dose, which is that amount that is effective to treat the particular asthma severity for which treatment is needed or otherwise desired.

[0413] D. Other Embodiments

[0414] From the above disclosure and examples, and from the claims below, the essential features of the invention are readily apparent. The scope of the invention also encompasses various modifications and adaptations within the knowledge of a person of ordinary skill. Examples include a disclosed compound modified by addition or removal of a protecting group, or an ester, pharmaceutical salt, hydrate, acid, or amide of a disclosed compound. Publications cited herein are hereby incorporated by reference in their entirety.

Claims

1. A method for preventing or treating asthma in patients, said method comprising the step of administering an antiasthmatic-effective amount of a MEK inhibitor to a patient in need of treatment, or to a patient suspected of developing asthma and in need of prophylactic treatment.

2. A method according to claim 1 wherein the patient being treated has been diagnosed as having asthma and is in need of treatment.

3. A method according to claim 1, wherein the MEK inhibitor is a selective MEK inhibitor.