CA2355470C

CA2355470C - Benzoheterocycles and their use as mek inhibitors

Info

Publication number: CA2355470C
Application number: CA002355470A
Authority: CA
Inventors: Stephen Douglas Barrett; Alexander James Bridges; Haile Tecle
Original assignee: Warner Lambert Co LLC
Current assignee: Warner Lambert Co LLC
Priority date: 1999-01-13
Filing date: 1999-12-21
Publication date: 2008-09-30
Anticipated expiration: 2019-12-21
Also published as: EP1144385B1; SK9832001A3; CN1177830C; NO20013452L; EP1144385A1; HUP0105113A3; BG105800A; TR200102030T2; NO20013452D0; HRP20010524A2; US6469004B1; IS5976A; WO2000042022A1; KR20020002370A; YU49401A; OA11746A; EE200100373A; DE69926800D1; HUP0105113A2; AP2001002224A0

Abstract

The invention provides compounds having formula (I), (see formula I) wherein W is OH, or derivatives of the carboxylic acid, and Q is a heterocyclo-condensed ortho-phenylene residue.
These compounds are useful as MEK inhibitors, particularly in the treatment of proliferative diseases such as cancer.

Description

BENZOHETEROCYCLES AND THEIR USE AS MEK INHIBITORS

This invention relates to benzoheterocycles such as benzoheteroaryis that have pharmacological activity.

BACKGROUND
MEK enzymes are duial specificity kinases involved in, for example, immunomodulation, inflammation, and proliferative diseases such as cancer and restenosis.
Proliferative diseases. are caused by a defect in the intracellular signaling system, or the signal transduction mechanism of certain proteins. Defects include a change either in thie intrinsic activity or in the cellular concentration of one or more signaling proteins in the signaling cascade. The cell may produce a growth factor that binds to its own receptors, resulting in an autocrine loop, which continually stimulates proliferation. Mutations or overexpression of intracellular signaling proteins can lead to spurious mitogenic signals within the cell.
Some of the most common mutations occur in genes encoding the protein known as Ras, a G-protein that is activated when bound to GTP, and inactivated when bound to GDP. The above-mentioned growth factor receptors, and many other mitogenic receptors, when activated, lead to Ras being converted from the GDP-bound state to the GTP-bound state. This signal is an absolute prerequisite for proliferation in most cell types. Defects in this signaling system, especially in the deactivation of the Ras-GTP complex, are common in cancers, and lead to the signaling cascade below Ras being chronically activated.
Activated Ras leads in turn to the activation of a cascade of serine/threonine kinases. C)ne of the groups of kinases known to require an active Ras-GTP for its own activation is the Raf family. These in turn activate MEK (e.g., MEK1 and MEK2) which then activates MAP kinase, ERK (ERK, and ERK2). Activation of MAP kinase by mitogens appears to be essential for proliferation; constitutive activation of this kinase is sufficient to induce cellular transformation. Blockade of downstream Ras signaling, for example by use of a dominant negative Raf-1 protein, can completely inhibit mitogenesis, whether induced from cell surface receptors or from oncogenic Ras mutants. Although Ras is not itself a protein kinase, it participates in the activation of Raf and other kinases, most likely through a phosphorylation mechanism. Once activated, Raf and other kinases phosphoryiate MEK on two closely adjacent serine residues, S218 and S222 in the case of MEK-1, which are the prerequisite for activation of MEK as a kinase. MEK in turn phosphorylates MAP kinase on both a tyrosine, Y185, and a threonine residue, T183, separated by a single amino acid. This double phosphorylation activates MAP kinase at least 100-fold. Activated MAP
kinase can then catalyze the phosphorylation of a large number of proteins, including several transcription factors and other kinases. Many of these MAP
kinase phosphorylations are rnitogenically activating for the target protein, such as a kinase, a transcription factor, or another cellular protein. In addition to Raf-1 and MEKK, other kinases activate MEK, and MEK itself appears to be a signal integrating kinase. Current understanding is that MEK is highly specific for the phosphorylation of MAP kinase. In fact, no substrate for MEK other than the MAP kinase , ERK, has been demonstrated to date and MEK does not phosphorylate peptides based on the MAP kinase phosphorylation sequence, or even phosphorylate denatured MAP kinase. MEK also appears to associate strongly with MAP kinase prior to phosphorylating it, suggesting that phosphorylation of MAP kinase by MEK may require a prior strong interaction between the two proteins. Both this requirement and the unusual specificity of MEK are suggestive that it rnay have enough difference in its mechanism of action to other protein kinases that selective inhibitors of MEK, possibly operating through allosteric mechanisms rather than through the usual blockade of the ATP
binding site, may be found.

SUMMARY
The invention features a compound having the formula (I) below:

0 H RIo wN

Rl l (I) In formula (I), W is OR,, NR;2ORI, NRARB, NR2NRARB, O(CH2)2-4NRARB, or NR2(CH2)2.4NRARB. Ri is H, C 1.8 alkyl, C 3_8 alkenyl, C 3.8 alkynyl, C 3-8 cycloalkyl, phenyl, (phenyl)C: ,.a alkyl, (phenyl)C 34 alkenyl, (phenyl)C 3-4alkynyl, (C 3-8 cycloalkyl)C 1.4alkyl, (C 3_8 cycloalkyl)C 3-4alkenyl, (C 3.8 cycloalkyl)C 3.4 alkynyl, C 3$ heterocyclic radical, (C 3-S heterocyclic radical)C I.4 alkyl, (C 3-8 heterocyclic radical)C 34 alkenyl, (C 3.8 heterocyclic radical)C 34 alkynyl or (CH2)2-4NRcRo. R2 is H, C1..a alkyl, phenyl, C 3-6 cycloalkyl, Cm heterocyclic radical, or (C 3-6 cycloalkyl) inethyl. RA is H, C1-6alkyl, C 3-8 alkenyl, C3-8 alkynyl, C 3.8 cycloalkyl, phenyl, (C 3-8 cycloalkyl)C 1-4alkyl, (C 3-8 cycloalkyl)C

3.4alkenyl, (C 3.8 cycloalkyl)C 3.4alkynyl, C 3.$ heterocyclic radical, (C 3.8 heterocyclic radical)C 1.4alkyl, (aminosulfonyi)phenyl, [(aminosulfonyl)phenyl]C 1.4alkyl, (aminosulfonyl)C 1.6 alkyl, (aminosulfonyl)C 3.6 cycloalkyi, [(aminosulfonyl)C
3.6 cycloalkyl]C 1-4alkyl, or (CH2)2-4NRcRo. RB is H, C1_S alkyl, C 3.$ alkenyl, C
3-$
alkynyl, C 3_$ cycloalkyl, or phenyl.

Q is one of the following forrnulae (i) - (iii):

,,,,,,,, ,,,,,,,, R3 ~ ~ R3 Z q ~
(1) (li) (lii) R3 is H or F; R4 is halo, NO2, SO2NRo(CH2)2.4NRERF, SO2NRERF or (CO)T. T is C 1_8 alkyl, C3.a cycloalkyl, (NRERF)C 1-4 alkyl, ORF, -NRo(CH2)2.4 NRERF, or NRERF; Z is one of the following formulae (iv) - (viii):

N N N\/Xl X2 N
\-41 (iv) (v) (vi) II II I I
N.X3N RG~ N.N;N
(vll), (viii) One of R5 and R6 is H or methyl and the other of R5 and R6 is H, C,-6alkyl, C2_6 alkenyl, CZ-6 alkynyl, phenyl, benzyl, or -M-E-G. M is 0, CO, SO2, NRi, (CO)NRH, NRH (CO), NRH (S02), (S02)NRH, or CH2. E is (CHZ),-4 or (CH2)m O(CH2)p where 1:5 (each of m and p) <_ 3 and 2:5 (m + p) <_ 4; or E is absent. G is RK, OR, or NRjRK, provided that if p = 1, then G is H. R7 is H, C1.4 alkyl, C 2.4 alkenyl, C 2-4alkynyl, C 3_6 cycloalkyl, phenyl, 2-pyridyl, 3-pyridyl, 4-pyridyl, (CH2)j_2Ar, where Ar is phenyl, 2-pyridyl, 3-pyridyl, or 4-pyridyl, SO2NRH(CH2)2-4NRjRK, (CO)(CH2)2_4NRjRK or (CO)NRH(CH2)2.4NRjR,c. X, is 0, S, NR8, or CHR9; X2 is 0, S, or CHR9; and X3 is 0 or S. In one embodiment, if X, or X2 is CHR9, the disclosed compound may also be a tautomerized indole. R8 is H, C 1-4alkyl, phenyl, 2-pyridyl, 3-pyridyl, 4-pyridyl, (CH2)1_2Ar, where Ar is phenyl, 2-pyridyl, 3-pyridyl, or 4-pyridyl, C 2.4alkenyl, C 24alkynyl, C3-6 cycloalkyl, or (C z4alkyl)NRLRM provided R7and Ra together have no more than 14 carbon atoms, exclusive of RL, RM, Rj and RK. Rc is C 1-4alkyl, phenyl, 2-pyridyl, 3-pyridyl, 4-pyridyl, C 3.4alkenyl, C 3-4alkynyl, C 3-6 cycloalkyl, (CO)ORP , (C 2.a alkyl)NRLRM, (CO)NRiq(CH2)2-4NRLRM, (CO)NRLRM, (CO)(CHZ)Z4-NRLRM, or (CH2)j_2Ar, where Ar is ptienyl, 2-pyridyl, 3-pyridyl, or 4-pyridyl. R9 is alkyl, phenyl, 2-pyridyl, 3-pyridyl, 4-pyridyl, C 2.4alkenyl, C 24alkynyl, C 3-6 cycloalkyl, (CO)ORP , (C 2-a alkyl)NRLRM, (CO)NRN(CH2)2_4NR,.RM, (CO)NRLRM, (CO)(CH2)24-NRLRM, or (CH2)1_2Ar', where Ar' is phenyl, 2-pyridyl, 3-pyridyl, or 4-pyridyl. Rp is H, C 1.6 alkyl, phenyl, C 3-4alkenyl, C3-4 alkynyl, C 3-6 cycloalkyl, or (CHZ)2-4NRLRM; RlQ is H, methyl, halo, or NO2; RI, is H, methyl, halo, or NO2. Each of Rc, Fto, RE, RF, R,, Ri, RK, RL and RM is independently selected from H, C 1.4alkyl, C 3.4alkenyl, C3.4alkynyl, C 3-6cycloalkyl, and phenyl; each of NRcRp,NRE,RF, NRjRK, and NRLRM can also independently be morpholinyl, piperazinyl, pyrrolidinyl, or piperadinyl. Each of RH, RN, and Ro is independently H, methyl, or ethyl. Finally, each hydrocarbon radical or heterocyclic radical above is optionally substituted with between 1 and 3 substituents independently selected from halo, C 1-4alkyl, C 3.6 cycloalkyl, C

alkenyl, C 24alkynyl, phenyl, hydroxyl, amino, (amino)sulfonyl, and NO2, wherein each substituent alkyl, cycloalkyl, alkenyl, alkynyl or phenyl is in turn optionally substituted with between 1 and 3 substituents independently selected from halo, C 1-2 alkyl, hydroxyl, amino, and NO2. In addition to the above compounds, the invention also provides a pharmaceutically-acceptable salt or C,_7 ester thereof.
The invention also relates to a pharmaceutical composition including (a) a benzoheterocycle (e.g., of formula l) and (b) a pharmaceutically-acceptable carrier.
The invention further relates to methods for treating proliferative diseases, such as cancer, restenosis, psoriasis, autoimmune disease, and atherosclerosis.
Other aspects of the inventicin include methods for treating MEK-related (including ras-related) cancers, whether solid or hematopoietic. Examples of cancers include colorectal, cervical, breast, ovarian, brain, acute leukemia, gastric, non-small cell lung, pancreatic and renal cancer. Further aspects of the invention include methods fcir treating or reducing the symptoms of xenograft (cell(s), organ, limb, skin, or bone marrow transplant) rejection, osteoarthritis, rheumatoid arthritis, cystic filbrosis, complications of diabetes (including diabetic retinopathy and diabetic nephropathy), hepatomegaly, cardiomegaly, stroke (such as acute focal ischemic stroke and global cerebral ischemia), heart failure, septic shock, asthma, and Alzheimer's disease. Compounds of the invention are also useful as antiviral agents for treating viral infections such as HIV, hepatitis (B) virus (HBV), human papillonia virus (HPV), cytomegalovirus (CMV), and Epstein-Barr virus (EBV). These methods include the step of administering to a patient in need of such treatment, or suffering from such a disease or condition, a pharmaceutically-effective amount of a disclosed compound or pharmaceutical composition thereof. Preferably, in the above methods of treatment, the compound of the invention is a selective MEK inhibitor.
The invention also features methods of combination therapy, such as a method for treating cancer, wherein the method further includes providing radiation therapy or chemotlnerapy, for example, with mitotic inhibitors such as a taxane or a vinca alkaloid. Examples of mitotic inhibitors include paclitaxel, docetaxel, vincristine, vinblastine, vinorelbine, and vinflunine. Other therapeutic combinations include a MEK inhibitor of the invention and an anticancer agent such as cisplatin, 5-fluorouracil (5FU), flutamide, and gemcitabine.

The chemotherapy or radiation therapy may be administered before, concurrently, or after the administration of a disclosed compound according to the needs of the patient.
The invention also features synthetic methods and synthetic intermediates disclosed herein.
Other aspects of the invention are provided in the description, examples, and claims below.

DETAILED DESCRIPTION
The invention features benzoheterocycle compounds, pharmaceutical compositions thereof, and methods of using such compounds and compositions.
According to one aspect of the invention, the compounds are MEK
inhibitors. MEK inhibition assays include the cascade assay for inhibitors of MAP
kinase pathway described at column 6, line 36 to column 7, line 4 of U.S.
Patent Number 5,525,625 and the in vitro MEK assay at column 7, lines 4-27 of the same patent, (see also Examples 22-25 below).
A. Terms Certain terms are defined below and by their usage throughout this disclosure.
Alkyl groups include aliphatic (i.e., hydrocarbyl or hydrocarbon radical structures containing hydrogen and carbon atoms) with a free valence. Alkyl groups are understood to include straight chain and branched structures.
Examples include methyl, ethyl, propyl, isopropyl, butyl, n-butyl, isobutyl, t-butyl, pentyl, isopentyl, 2,3-dimethyipropyi, hexyl, 2,3-dimethylhexyl, 1,1-dimethylpentyl, heptyl, and octyl. Cycloalkyl groups include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, and cyclooctyl.
Alkyl groups can be substituted with 1, 2, 3 or more substituents which are independently selected from halo (fluoro, chloro, bromo, or iodo), hydroxy, amino, alkoxy, alkylamino, dialkylamino, cycloalkyl, aryl, aryloxy, arylalkyioxy, heterocyclic radical, and (heterocyclic radical)oxy. Specific examples include fluoromethyl, hydroxyethyl, 2,3-dihydroxyethyl, (2- or 3-furanyl)methyl, cyclopropylmethyl, benzyloxyethyl, (3-pyridinyl)methyl, (2- or 3-furanyl)methyl, (2-thienyl)ethyl, hydroxypropyl, aminocyclohexyl, 2-dimethylaminobutyl, methoxymethyl, N-pyridinyleithyl, diethylaminoethyl, and cyclobutylmethyl.
Alkenyl groups are analogous to alkyl groups, but have at least one double bond (two adjacent spz carbon atoms). Depending on the placement of a double bond and substituents, if any, the geometry of the double bond may be entgegen (E), or zusammen (Z), cis, or trans. Similarly, alkynyl groups have at least one triple bond (two adjacent sp carbon atoms). Unsaturated alkenyl or alkynyl groups may have one or moire double or triple bonds, respectively, or a mixture thereof; like alkyl groups, unsaturated groups may be straight chain or branched, and they may be substituted as described both above for alkyl groups and throughout the disclosure by example. Examples of alkenyls, alkynyls, and substituted forms include cis-2-butenyl, trans-2-butenyl, 3-butynyl, 3-phenyl-propynyl, 3-(2'-fluorophenyl)-2-propynyl, 3-methyl(5-phenyl)-4-pentynyl, 2-hydroxy-2-propynyl, 2-methyl-2-propynyl, 2-propenyl, 4-hydroxy-3-butynyl, 3-(3-fluorophenyl)-2-propynyl, and 2-methyl-2-propenyl. In formula (I), alkenyl and alkynyl groups can be, for example, C 2-4 or C 2.8, and are preferably C34 or CM.
More general forms of substituted hydrocarbon radicals include hydroxyalkyl, hydroxyalkenyl, hydroxyalkynyl, hydroxycycloalkyl, hydroxyaryl, and corresponding forms for the prefixes amino-, halo- (e.g., fluoro-, chioro-, or bromo-), nitro-, alkyl-, phenyl-, cycloalkyl- and so on, or combinations of substituents. According to formula (I), therefore, substituted alkyls include hydroxyalkyl, aminoalkyl, nitroalkyl, haloalkyl, alkylalkyl (branched alkyls, such as methylpentyl), (cycloalkyl)alkyl, phenylalkyl, alkoxy, alkylaminoalkyl, dialkylaminoalkyl, arylalkyl, aryloxyalkyl, arylalkyloxyalkyl, (heterocyclic radical)alkyl, and (heterocyclic radical)oxyalkyl. R, thus includes hydroxyalkyl, hydroxyalkenyl, hydroxyalkynyl, hydroxycycloalkyl, hydroxyaryl, aminoalkyl, aminoalkenyl, aminoalkynyl, aminocycloalkyl, aminoaryl, alkylalkenyl, (alkylaryl)alkyl, (haloaryl)alkyl, (hydroxyaryl)alkynyl, and so forth.
Similarly, RA

includes hydroxyalkyl and aminoaryl, and RB includes hydroxyalkyl, aminoalkyl, and hydroxyalkyl(heterocyclic radical)alkyl.
Heterocyclic radicals, which include but are not limited to heteroaryls, include: furyl, oxazolyl, isoxazolyl, thiophenyl, thiazolyt, pyrrolyl, imidazolyl, 1,3,4-triazolyl, tetrazolyl, pyridinyl, pyrimidinyl, pyridazinyl, indolyl, and their nonaromatic counterparts. Further examples of heterocyclic radicals include piperidyl, quinolyl, isothiazolyl, piperidinyl, morpholinyl, piperazinyl, tetrahydrofuryl, tetrahydropyirrolyl, pyrrolidinyl, octahydroindolyl, octahydrobenzothiofuranyl, and octahydrobenzofuranyl.
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 ME:K 2 that is at least one-fiftieth (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 1/100, more preferably 1/500, and even more preferably 1/1000, 1/5000, or less than that of its IC5o or one or more of the above-named enzymes.

B. Compounds One aspect of the invention features disclosed compounds shown in formula (I) in the Summary section. Embodiments of the invention includes compounds of formula (I) wtierein: (a) Q is formula (i); (b) R3 is H or fluoro;
(c) R4 is fluoro, chloro, or bromo; (d) Rio is H, methyl, fluoro, or chloro;
(e) RI, is methyl, chloro, fluoro, nitro, or hydrogen; (f) Rl I is H; (g) R is fluoro;
(h) each of Rio and Ri, is fluoro; (i) R, is H, methyl, ethyl, propyl, isopropyl, isobutyl, benzyl, phenethyl, allyl, C 3_r, alkenyl, C 3-6cycloalkyl, (C 3-5 cycloalkyl)C 1.2 alkyl, (C 3-5 heterocyclic radical)C 1-2 alkyl, or (CH2)2-4NRcRo; (j) R, is H or (C 3-cycloalkyl)C 1-2 alkyl; (k) R2 iis H or methyl; (I) RA has at least one hydroxyl substituent; (m) RA is H, methyl, ethyl, isobutyl, hydroxyethyl, phenyl, 2-piperidin-1-yl-ethyl, 2,3-dihydroxy-propyl, 3-[4-(2-hydroxyethyl)-piperazin-1-yl]-propyl, 2-pyrrolidin-1-yl-ethyl, or 2-diethylamino-ethyl; and RB is H; or where RB is methyl and RA is phenyl.; (n) W is NRARB or NR2NRARB; (o) W is NR2(CH2)2.4NRARB or O(CH2)2_3 NRARB; (p) W is NRZORj; (q) W is OR,; (r) Z is formula (v); or (s) X, is NR8, and R7 is H; or (t) conibinations thereof. In formula (I), the values for Z are shown left to right, or in a counter-clockwise orientation around the phenyl ring of Q.
According to one aspect of the invention, the compound of formula (I) has a structure wherein: Q is foi-mula (i) or (ii); R3 is H or fluoro; R4 is fluoro, chloro, or bromo; Rio is H, methyl, or chloro; Rl I is chloro, fluoro, or hydrogen; R, is H, methyl, ethyl, propyl, isopropyl, isobutyl, benzyl, phenethyl, allyl, C3-5 alkenyl, C 3.
6 cycloalkyl, (C 3-5 cycloalkyl)C 1-2 alkyl, (C 3_5 heterocyclic radical)C 1-2 alkyl, or (CH2)2.4NRcRp; R, is H or (C 3.4cycloalkyl)C 1-2 alkyl; R2 is H or methyl; and Z is formula (v) or (vi). One emibodiment of this aspect, X, is NRa. An example would be 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1 [(2'-morpholinyl)-ethylj-2-(phenyl)-benzoimidazole-5-carboxylic acid cyclopropylmethoxy-amide.
Embodiments of the invention also include compounds wherein Rio is H;
Rio is methyl or chloro; and where Rio is chloro. In some embodiments, R7 and R8 together have no more than 14 carbon atoms, exclusive of RL, Rnn, Rj and RK.
Examples of this include compounds wherein R7and R8 together have no more than 13 carbon atoms; no rnore than 7, 8, or 10 carbon atoms; between 4 and 8 carbon atoms; between 1 and 10 carbon atoms; between 1 and 8 carbon atoms;
and no more than 6 carbon atoms.
Preferably, where one of R,, R2, RA, RB, Rc, Rp, RE, RF, R,, Rj, RK, RL, RM, RG, RH, RN, Ro, and RP is an alkenyl or alkynyl group, its double or triple bond, respectively, is not adjacent the point of attachment. For example, where W is NRZOR,, R2 is preferably prop-2-ynyl, or but-2 or 3-enyl, and less preferably prop-1-ynyl or but-l-enyl.
Listed below are some of the preferred structures which can be synthesized utilizing Schemes 1, 2, 10, and 11. Free acids, free hydroxamic acids, and cyclopropylmethyl hydroxamates are grouped together. For example, compounds 1, 11, and 21 differ only by "W" (as defined in the claims);
compounds 2, 12, and 22 are similarly related. Preferred compounds also include the 2-chloro (replacing 2-methyl) analogs of the listed compounds.
Compound Number Compound Name 7-Fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-1. benzoimidazole-5-carboxylic acid (PD 205293;
APK IC = 47 17 nM) 2 7-Fluoro-6-(4-iodo-2-methyl-phenylamino)-benzooxazole-5-carbox lic acid 3 7-Fluoro-6-(4-iodo-2-methyl-phenylamino)-benzothiazole-5-carbox lic acid 4 7-Fluoro-6-(4-iodo-2-methyl-phenylamino)-benzo 1 2 5 thiadiazole-5-carbox lic acid 5. 7-Fluoro-6-(4-iodo-2-methyl-phenylamino)-benzo 1,2,5 oxadiazole-5-carbox lic acid 7-Fluoro-6-(4-iodo-2-methyl-phenylamino)-2-(2-6. hydroxyethyl)-1 H-benzoimidazole-5-carboxylic acid 7-Fluoro-6-(4-iodo-2-methyl-phenylamino)-2-(2-7. dimethylamino-ethyl)-1 H-benzoimidazole-5-carbox lic acid 8 7-Fluoro-6-(4-iodo-2-methyl-phenylamino)-1-acet I-benzoimidazole-5-carbox lic acid 9 8-Fluoro-7-(4-iodo-2-methyl-phenylamino)-uinoxaline-6-carbox lic acid 10. 7-Fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzotriazole-5-carbox lic acid 11. 7-Fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzoimidazole-5-carbox lic acid h drox amide Compound Number Compound Name 12 7-Fluoro-6-(4-iodo-2-methyl-phenylamino)-benzooxazole-5-carbox lic acid h drox amide 13. 7-Fluoro-6-(4-iodo-2-methyl-phenylamino)-benzothiazole-5-carbox lic acid h drox amide 7-Fluoro-6-(4-iodo-2-methyl-phenylamino)-14. benzo[1,2,5]thiadiazole-5-carboxylic acid h drox amide 7-Fluoro-6-(4-iodo-2-methyl-phenylamino)-15. benzo[1,2,5]oxadiazole-5-carboxylic acid h dro amide 7-Fluoro-6-(4-iodo-2-methyl-phenylamino)-2-(2-16. hydroxyethyl)-1 H-benzoimidazole-5-carboxylic acid h drox amide 7-Fluoro-6-(4-iodo-2-methyl-phenylam i no)-2-(2-17. dimethylamino-ethyl)-1 H-benzoimidazole-5-carbo lic acid h dro amide 7-Fluoro-6-(4-iodo-2-methyl-phenylamino)-1-18. acetyl-benzoimidazole-5-carboxylic acid h dro amide 19 8-Fluoro-7-(4-iodo-2-methyl-phenylamino)-uinoxaline-6-carbo lic acid h dro amide 20 7-Fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzotriazole-5-carbo lic acid h dro amide 7-Fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-21. benzoimidazole-5-carboxylic acid cVclop ro Imetho -amide 7-Fluoro-6-(4-iodo-2-methyl-phenylam ino)-22. benzooxazole-5-carboxylic acid c clo ro Imethox -amide 7-Fluoro-6-(4-iodo-2-methyl-phenylamino)-23. benzothiazole-5-carboxylic acid cyclop ro Imetho -amide 7-Fluoro-6-(4-iodo-2-methyl-phenylamino)-24. benzo[1,2,5]thiadiazole-5-carboxylic acid c clo ro Imetho -amide 7-Fluoro-6-(4-iodo-2-methyl-phenylamino)-25. benzo[1,2,5]oxadiazole-5-carboxylic acid c clo ro Imetho -amide 7-Fluoro-6-(4-iodo-2-methyl-phenylamino)-2-(2-26. hydroxyethyl)-1 H-benzoimidazole-5-carboxylic acid c clo ro Imetho -amide 7-Fluoro-6-(4-iodo-2-methyl-phenylamino)-2-(2-27. dimethylamino-ethyl)-1 H-benzoimidazole-5-carbox lic acid c clo ro Imethox -amide Compound Number Compound Name 7-Fluoro-6-(4-iodo-2-methyl-phenylamino)-1-28. acetyl-benzoimidazole-5-carboxylic acid c clo ro Imethox -amide 8-Fluoro-7-(4-iodo-2-methyl-phenylamino)-29. quinoxaline-6-carboxylic acid c clo ro Imetho -amide 7-Fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-30. benzotriazole-5-carboxylic acid c clo ro Imethox -amide The following is a list of examples representing schemes 3-9. As above, free acids, free hydroxamic acids, and cyclopropylmethyl hydroxamates are grouped together. For example, compounds 31, 45, and 59 differ only by "W"
(as defined in the claims); compounds 32, 46, and 60 are similarly related.
Preferred compounds also include the 2-chloro (replacing 2-methyl) analogs of the listed compounds.

Compound Number Compound Name 31. 4-Fluoro-5-(4-iodo-2-methyl-phenylamino)-benzothiazole-6-carbo lic acid 32 4-Fluoro-5-(4-iodo-2-methyl-phenylamino)-benzooxazole-6-carbo lic acid 33. 5-(2-Chloro-4-iodo-phenylamino)-6,7-difluoro-3H-benzoimidazole-4-carbo lic acid 6,7-Difluoro-2-(2-hydroxy-ethyl)-5-(4-iodo-2-34. methyl-phenylamino)-3H-benzoimidazole-4-carbox lic acid 35. 6,7-Difluoro-5-(4-iodo-2-methyl-phenylamino)-benzooxazole-4-carbo lic acid 36. 6,7-Difluoro-5-(4-iodo-2-methyl-phenylam i no)-benzothiazole-4-carbo lic acid 37 7,8-Difluoro-6-(4-iodo-2-methyl-phenylamino)-uinoxaline-5-carbo lic acid 38 6-(4-lodo-2-methyl-phenylamino)-8-nitro-uinoxaline-5-carbo lic acid 39. 5-(4-lodo-2-methyl-phenylamino)-8-nitro-uinoxaline-6-carbo lic acid 40. 8-Chloro-5-(4-iodo-2-methyl-phenylamino)-uinoxaline-6-carbo lic acid Compound Number Compound Name 3-Cyclopropyl-7-(4-iodo-2-methyl-phenylamino)-41. 3H-benzoimidazole-4,6-dicarboxylic acid 4-dimeth lamide 42 7-Bromo-4-(4-iodo-2-methyl-phenylamino)-benzooxazole-5-carbox lic acid 43. 7-(2-Chloro-4-iodo-phenylamino)-4-fluoro-benzothiazole-6-carbo lic acid 44. 7-(4-Iodo-2-methyl-phenylamino)-4-nitro-benzooxazole-6-carbox lic acid 45. 4-Fluoro-5-(4-iodo-2-methyl-phenylamino)-benzothiazole-6-carbo lic acid h dro amide 46 4-Fluoro-5-(4-iodo-2-methyl-phenylamino)-benzooxazole-6-carbox lic acid h drox amide 47 5-(2-Chloro-4-iodo-phenylamino)-6,7-difluoro-3H-benzoimidazole-4-carbo lic acid h dro amide 6,7-Difluoro-2-(2-hyd roxy-ethyl)-5-(4-iodo-2-48. methyl-phenylamino)-3H-benzoimidazole-4-carbo lic acid h dro amide 49 6,7-Difluoro-5-(4-iodo-2-methyl-phenylamino)-benzooxazole-4-carbox lic acid h drox amide 50. 6,7-Difluoro-5-(4-iodo-2-methyl-phenylamino)-benzothiazole-4-carbo lic acid h dro amide 51. 7, 8-Difluoro-6-(4-iodo-2-methyl-phenylamino)-uinoxaline-5-carbox lic acid h drox amide 52 6-(4-Iodo-2-methyl-phenylamino)-8-nitro-uinoxaline-5-carbo lic acid h dro amide 53. 5-(4-Iodo-2-methyl-phenylamino)-8-nitro-uinoxaline-6-carbox lic acid h drox amide 54. 8-Chloro-5-(4-iodo-2-methyl-phenylamino)-uinoxaline-6-carbo lic acid h dro amide 3-Cyclopropyl-7-(4-iodo-2-methyl-phenylamino)-55. 3H-benzoimidazole-4,6-dicarboxylic acid 4-dimeth lamide 6-h drox amide 56. 7-Bromo-4-(4-iodo-2-methyl-phenylamino)-benzooxazole-5-carbo lic acid h dro amide 57 7-(2-Chloro-4-iodo-phenylamino)-4-fluoro-benzothiazole-6-carbox lic acid h drox amide 58 7-(4-Iodo-2-methyl-phenylamino)-4-nitro-benzooxazole-6-carbo lic acid h dro amide 4-Fluoro-5-(4-iodo-2-methyl-phenylamino)-59. benzothiazole-6-carboxylic acid c clo ro Imetho -amide 4-Fluoro-5-(4-iodo-2-methyl-phenylamino)-60. benzooxazole-6-carboxylic acid c clo ro Imethox -amide Compound Number Compound Name 5-(2-Chloro-4-iodo-phenylamino)-6,7-difluoro-3H-61. benzoimidazole-4-carboxylic acid c clo ro Imethox -amide 6,7-D ifl uoro-2-(2-hyd roxy-ethyl)-5-(4-iodo-2-62. methyl-phenylamino)-3H-benzoimidazole-4-carbox lic acid c clo ro Imethox -amide 6,7-Difluoro-5-(4-iodo-2-methyl-phenylamino)-63. benzooxazole-4-carboxylic acid c clo ro Imethox -amide 6,7-Difluoro-5-(4-iodo-2-methyl-phenylamino)-64. benzothiazole-4-carboxylic acid c clo ro Imethox -amide 7, 8-Difluoro-6-(4-iodo-2-methyl-phenylamino)-65. quinoxaline-5-carboxylic acid cyclopropylmethoxy-amide 6-(4-lodo-2-methyl-phenylamino)-8-nitro-66. quinoxaline-5-carboxylic acid cyclopropylmethoxy-amide 5-(4-lodo-2-methyl-phenylamino)-8-nitro-67. quinoxaline-6-carboxylic acid cyclopropylmethoxy-amide 8-Chloro-5-(4-iodo-2-methyl-phenylamino)-68. quinoxaline-6-carboxylic acid cyclopropylmethoxy-amide 3-Cyclopropyl-7-(4-iodo-2-methyl-phenylamino)-69. 3H-benzoimidazole-4,6-dicarboxylic acid 4-dimeth lamide 6-c clo ro Imethox -amide 7-Bromo-4-(4-iodo-2-methyl-phenylamino)-70. benzooxazole-5-carboxylic acid c clo ro Imetho -amide 7-(2-Chloro-4-iodo-phenylamino)-4-fluoro-71. benzothiazole-6-carboxylic acid c clo ro Imethox -amide 7-(4-lodo-2-methyl-phenylamino)-4-nitro-72. benzooxazole-6-carboxylic acid c clo ro Imethox -amide.

C. Synthesis The disclosed compounds can be synthesized according to the following eleven Schemes, or variants thereof. These synthetic strategies are further exemplified in Examples 1-22 below.

14a Scheme 1 HO O HO O

Ll H-Xi R8 9 Ll H-O-R12 /
02N R3 O2N R3 Catalyst L2 X l H R8a9 Rt 2 O O R1 ~2O O H Rlo ~L' RtBase N + H2N02N X1 R3 Rt 02N XtR3 Rtl H R8a 9 H R8 9 R1 z O o H Rlo 0 R12 O O N Rto Reducing Agent ZN b L21~ R7 I~
H N N /
2 X tR3 Rll ~{l R3 R11 ~
R8 a 9 H R8 a 9 R7 ~O O
Rt 2 H R1o lodinating Reagent ~ N Deesterification I ~ I
N~X1 R3 Rll R7 R8 u 9 HO O H lo R R1=O.N O H Rlo H

N\X 1 R3 R N\\ ~{ 1 R3 R l 1 R7 R8 v 9 R7 R8 a 9 Scheme 2 R12 O O Rto Rt2 0 0 H Rto I\ L~
+ H2N Base N
]I i i I
02N NH R3 Rt 02N
NH2R3 Rt l O ~ ~ O O
~O. 0 RR6 Rt2 H Rto Rto 5 O N
Reducing Agent Rt2 H
~ ~ - -- , (, N R3 Rt t H2N NIõ~2R3 Rtt R5 ~O O
Rt2 H Rio lodinating Reagent N I Deesterification - - I~ ~ -N R3 Rti HO O H Rto Rt.O.N O HRto N ~ R2-N H -O-Rt N ~
~ / -- - I , ~ , N j N R3 Rtt N~N R3 Rlt I
R5 Rs Scheme 3 HO O HO O
R13 Lt ~ Lt H-N-RL4I H-O-R12 O N R Base ~ O2N R3 Catalyst 2 3 .
L2 R13~ N R14 R12 'O O Rto R1z"' O 0 H Rlo + H2N Base ( N I ~
I Ll 02N R3 R I I ~ 02N ~ R /
N. ~N 3 R11 Rt3~ Rla Rt3 R14 ~O O " O O
R 12 R Rt2 H Rto Reducing Agent N ~ 1) Diazotization N

H NJ ~~ 2) M2 I/ R R
2 R3 R11 ~N. 3 11 R13,N. R14 R13 R14 ~O O
Rt2 H R1o 0 -'O O
Deprotection N R12 H Rto I I-'2AR7 N ~
HX2 I ( ~
NH2R3 Rt l X~N R3 Rl t ~O
Rlz H R1o lodinating Reagent I N ~ Deesterification , , 1 . -XZ~:--N R3 R l t HO O H Rlo R1.O.N O H R
to N ~\ R2-NH -O-Rt I N
/ i I I
X2~,_N R3 Rl t X2R3 Rl t R~7' R7 Scheme 4 HO O HO O HO O
Ll ~ Ll Nitration L, H-X2=Rgor9 ~2 Li I -~ ( R8 or 9 Ra R4 R4 R1Z O 0 R R,2' O O H Rto H-O-R12 X2 La H2N \ Base R _X2 I N t R8 or 9 + I 8 or 9 / Catalyst 02N R3 / 02N
Rli R3 R~]

Ra Z
Reducing Agent R1~2 N R\ L2 R7 R8 or 9 XZ H

R8 or 9 ~/ R7 \\ H2'y N R
R4 R3 R~, R4 3 Rtt " O O HO O R
R12 H Rio R H ~o g~' 9 /X2 N I~
lodinating Reagent RR7' 9 X21I N I~ Deesterification R
\
-' Ra R3 Ri, R4 R3 Rii RZ
R1,O,N O
R~o H_ Rg or 9 X2 N ~

R~ N~I I ~ l R4 R3 R, l Scheme 5 HO O HO O HO O
Rt3~N L
Lt ~ Lt Nitration LI L1 R13-N-Rta Rta I 1 R3 O2N ( R3 O2N R4 Ra Ra ~O O
R12 O O Rto R22 H Rto H-O-R12 Rt3~N LI H N Base Rt3;N N ~
Rta I + 2 ~ Rta ~
Catalyst O2N ~=p,3 Rl t I~ 02N
Ra R3 R/

O O
Rt - O O z Rtz H Rt0 Reducing Agent Rt3;N H I)Diazotization Rt14;N N ta H2Td I2) ~Xt R3 Rt Ra Rs Rtt Ra R12 O, O H Rlo 0 Rt2 O O H Rto Deprotection H2N ~ N ~ L~ R2 N N
HX~ R2--~X R
t R R3 Rt1 3 Rtt " O ,O HO 0 R
R12 H Rtp H to lodinating Reagent N N Deesterification N N ~ I
Xt R7-{~ R7~
~, Xt R,I R3 Rl t R3 Rt 1 RI.O,N ,O H Rto R2-N-O-Rt N
i R2---Xt Res R3 R t t Scheme 6 HO O HO O HO O
Ll ~ Ll Nitration Ll ~ Ll NH3 H2N Ll R3 02N I~ R3 O2N R3 Ra R4 R4 R
~O O 2 O O
l2 Rlp R1 H Rlo H-0-R12 H2N Ll + ( H2N \ Base ONI
Catalyst 02N ~ P: ~ 2 3 Ri l Ra Ra R3 Rl l Reducing Agent R12 O. 0 H Rlo Rs~R6 R12 O 0 Rlo H H2N, N ~ 0 Rs N N ~

H2N~I ~ I~
Ra R3 Rll R6 N R4 R3 Rl1 HO O
"O ~O
R12 H Rlo H lo lodinating Reagent R5 N Deesterification RsN N

R6 N R3 Rl l a ~/ N I
~ R R3 Rl t Ra H RI.O.N O H Rlo R2 N-O-RI R5 N ~N
~~N I I ~ I
R4 R3 Rll Scheme 7 HO O HO O HO O
R4 ~ Lt Nitration Ra I~ Lr NH3 R4 I~ Lt R3 R3 Np2 R3 ~ NOZ
L~ Lt NH2 R12 p O Rio Rtz" O O H Rio H-O-R12 4 1 Lt + H2N Base R4 N ~
~
i Catalyst R3 M NO2 Ri t ~ R3 NH2N02 Rt I
z 0 ~O O
~O O ~~ RRt2 H RIo R12 H Rio R54 N
Reducing Agent R4~, N ~ 0 /) ~ / R3 N Ru R3 ~ NH2 Rt t NR6 Z R
s ~O
R~Z H Rlo HO O H Rio lodinating Reagent R4 N Deesterification R4 N

Rg N I~ Rtt I R3 N I/ I
~ KN Rit Rb Rb R, RI,,N;O
p H Rio H
R2-N-O-Rt R4 N

N~. ' RI t Scheme 8 HO O HO O HO O
R4 ~ Lt Nitration R4 ~ Lt H-X2'R8 or9 R4 ~ Lt LI Lt H Rg or9 Rt20 O Rt2 O O H Rto H-O-R12 4 (~ Li +~..~2N ~ Base R4 N
Catalyst R3 r lNO2 R I i R3 NO2 Rt i }{2 t t X2 H R8or9 H R8or9 F:12 O O H Rtp IOi Rt2 O O H Rio Reducing Agent R4 N ~ L2/~ R7 R4 ~ N t I~~ ~~ R3 NH2 R i t R3 X2~ Rl t X2 ~
H Rgor9 R8or9 R7 ~O O HO O
R12 H Rtp H Rtp lodinating Reagent R4 N ~ Deesterification R4 N ~
R3~ N I / R3 ~ / N I

}(2A Rtt X2!~ Rli R8 or 9 R7 R8 or 9 R7 RI,O,N. ~O R
H H to R2-I.I-O-RI R4 =~ N ~
R
3 1j N ~ /
' X2A Rt t i R8 or 9 R7 Scheme 9 HO O HO O HO O
R4 R4; Lt H R4 Lt Nitration R13-N-Rt4_ I
R3 R3 NOz R3 N. NOz L~ L, R13' Rt4 ' O O ~O O
Rt2 Rtz H Rto H-0-R12 _ 4 Lt H N R10 Base R4 N
z Catalyst R3 NOz + R3 ~N R .N. NOzR>>
R13 Rta R13 R14 R12 O O H R10 R12 O O H Rio Reducing Agent R4~ -- N 1) Diazotization R4 N
2)Mi-R3 NH2R,l R3 N. XIHRtt Rj;3' R14 Rt. s R14 z 0 "O O
"O O Rt ~ R12 H Rto Deprotection R1 H Lz Rz R4 N

tR
R3/ NH2 N=~ tt z R7 Q, p HO O
Rtz H R~o H R~o lodinating Reagent R4)I N I~ Deesterification R4 ' N I
i R3 Xi R R3 Xt R
N~ tt N=/ tt R7 \R7 R.z Rt,,1i, O
H O H RIo Rz-N-O-RI R4 N
)~i Ii R3 N~ ) Rtt I

Scheme 10 ,o 0 Rl Z O O H R10 R1 2 H Rlo N Reagents - / I N

A N.~R3 R11 X3 N R3 Rll A=N02 or NH2 R12 O O H Rlp lodinating Reagent (IR3 N Deesterification HO O R RI, O' N O Rlo H lo H H

- - ~ I
~ ~
N, R3 R11/ N~ N R3 R11 )~3 N X3 Scheme 11 ,o o ,o 0 R12 H Rto R12 H Rto I N I RG-L3 i I N

HN ~N
2 ~ R3 RI, H~N. R3 Rtt ~O O
R12 H Rto Deprotection N Diazotization RG.N ~.

R12 o 0 H Rto R1i 0 0 H Rto I N I lodinating Reagent i f N

RG_N RG_N I
=N R3 Rl l N R3 Rt t Ho O
H Rto H
Deesterification \ I N I R2-N-O-R1 RG..N I --.
~N R3Rt1 Rl,,N O
~ H Rlo N
I Ii RG-N R3 Rt t I
N=N

D. Uses The disclosed compositions are useful as both prophylactic and therapeutic treatments for diseases or conditions as provided in the Summary section, as well as diseases or conditions modulated by the MEK cascade.
Examples include stroke, heart failure, osteoarthritis, rheumatoid arthritis, organ transplant rejection, and a variety of tumors such as ovarian, lung, pancreatic, brain, prostatic, and colon.
1. Dosages Those skilled in the airt will be able to determine, according to known methods, the appropriate dosage for a patient, taking into account factors such as age, weight, general health, the symptoms requiring treatment, and the presence of other medications. In genieral, an effective amount will be between 0.1 and 1000 mg/kg per day, preferably between 1 and 300 mg/kg body weight, and daily dosages will be between 10 and 5000 mg for an adult subject of normal weight.
Capsules, tablets or other formulations (such as liquids and film-coated tablets) may be of between 5 and 200 mg, such as 10, 15, 25, 35, 50 mg, 60 mg, and 100 mg can be administered according to the disclosed methods.
2. Formulations Dosage unit forms include tablets, capsules, pills, powders, granules, aqueous and nonaqueous oral solutions and suspensions, and parenteral solutions packaged in containers adapted for subdivision into individual doses.
Dosage unit forms can also be adapted for various methods of administration, including controlled release formulations, such as subcutaneous implants.
Administration methods include oral, rectal, parenteral (intravenous, intramuscular, subcutaneou:s), intracisternal, intravaginal, intraperitoneal, intravesical, local (drops, powders, ointments, gels, or cream), and by inhalation (a buccal or nasal spray).
Parenteral formulations include pharmaceutically acceptable aqueous or nonaqueous solutions, dispersion, suspensions, emulsions, and sterile powders for the preparation thereof. Examples of carriers include water, ethanol, polyols (propylene glycol, polyethylene glycol), vegetable oils, and injectable organic esters such as ethyl oleate. Fluidity can be maintained by the use of a coating such as lecithin, a surfactant, or maintaining appropriate particle size.
Carriers for solid dosage forms include (a) fillers or extenders, (b) binders, (c) humectants, (d) disintegrating agents, (e) solution retarders, (f) absorption accelerators, (g) adsorbants, (h) lubricants, (i) buffering agents, and 0) propellants.
Compositions may also contain adjuvants such as preserving, wetting, emulsifying, and dispensing agents; antimicrobial agents such as parabens, chlorobutanol, phenol, and sorbic acid; isotonic agents such as a sugar or sodium chloride; absorption-prolonging agents such as aluminum monostearate and gelatin; and absorption-enhancing agents.
In a preferred embodiment, the invention comprises a commercial package comprising a container containing a composition comprising the compound of formula (I) and a pharmaceutically acceptable carrier and written matter which states that the composition is for use in the treatment of a medical condition selected from:
a) a proliferative disease;
b) cancer;
c) osteoarthritis;
d) rheumatoid arthritis;
e) a viral infection;
f) cystic fibrosis;
g) hepatomegaly;
h) cardiomegaly;
i) Alzheimer's disease;
j) a complication of diabetes;
k) septic shock; and I) asthma.
In another preferred embodiment, the invention comprises a commercial package comprising a container containing a compound of formula (I) and written matter which states that the compound is for use in the treatment of a medical condition selected from:
a) a proliferative disease;
b) cancer;

c) osteoarthritis;
d) rheumatoid arthritis;
e) a viral infection;
f) cystic fibrosis;
g) hepatomegaly;
h) cardiomegaly;
i) Alzheimer's disease;
j) a complication of diabetes;
k) septic shock; and I) asthma.
In a further preferred embodiment, the invention comprises a commercial package comprising a container containing a composition comprising a compound of formula (I) and a pharmaceutically acceptable carrier and written matter which states that the composition is for use in the treatment or amelioration of the symptoms of a medical condition selected from:
a) sequelae of a stroke;
b) sequelae of heart failure; and c) xenograft rejection.
In a further preferred embodiment, the invention comprises a commercial package comprising a container containing a compound of formula (I) and written matter which states that the compound is for use in the treatment or amelioration of the symptoms of a medical condition selected from:
a) sequelae of a stroke;
b) sequelae of heart failure; and c) xenograft rejection.

3. Related compounds The invention provides the disclosed compounds and closely related, pharmaceutically acceptable forms of the disclosed compounds, such as salts, esters, amides, hydrates or solvated forms thereof; masked or protected forms;
and racemic mixtures, or enantiomerically or optically pure forms.

27a Pharmaceutically acceptable salts, esters, and amides include carboxylate salts (e.g., C,., alkyl, cycloalkyl, aryl, heteroaryl, or non-aromatic heterocyclic), amino acid addition salts, esters, and amides which are within a reasonable benefit/risk ratio, pharmacologically effective, and suitable for contact with the tissues of patients without undue toxicity, irritation, or allergic response.
Representative salts include 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 laurylsulfonate. These may include alkali metal and alkali earth cations such as sodium, potassium, calcium, and magnesium, as well as non-toxic ammonium, quaternary ammonium, and amine cations such as tetramethyl ammonium, methylamine, trimethylamine, and ethylamine. See, for example, S.M. Berge, et al., "Pharmaceutical Salts," J. Pharm. Sci., 1977, 66:1-19. Representative pharmaceutically acceptable amides of the invention include those derived from ammonia, primary C,,. alkyl amines and secondary di (C ., alkyl) amines.
Secondary amines include 5- or 6-membered heterocyclic or heteroaromatic ring moieties containing at least one nitrogen atom 27b and optionally between 1 and 2 additional heteroatoms. Preferred amides are derived from ammonia, C1;3 alkyl primary amines, and di (C 1_2 alkyl)amines.
Representative pharmaceutically acceptable esters of the invention include C,_7 alkyl, Cf,, cycloalkyl, phenyl, and phenyl(C 1-6)alkyl esters. Preferred esters include methyl esters.
The invention also includes disclosed compounds having one or more functional groups (e.g., hydiroxyl, amino, or carboxyl) masked by a protecting group. Some of these maslced or protected compounds are pharmaceutically acceptable; others will be useful as intermediates. Synthetic intermediates and processes disclosed herein, and minor modifications thereof, are also within the scope of the invention. Exaimples of synthetic intermediates of the invention include PD 202885, PD 203337, PD 218001, PD 254551, and PD 201601.
HYDROXYL PROTECTING GROUPS
Hydroxyl protecting groups include: ethers, esters, and protection for 1,2-and 1,3-diols. The ether protecting groups include: methyl, substituted methyl ethers, substituted ethyl ethers, substituted benzyl ethers, silyl ethers and conversion of silyl ethers to other functional groups.
Substituted Methyl Ethers Substituted methyl ethers iriclude: methoxymethyl, methylthiomethyl, t utylthiomethyl, (phenyldimethylsilyl) methoxymethyl, benzyloxymethyl, p-ethoxybenzyloxymethyl, (4-methoxyphenoxy) methyl, guaiacolmethyl, t-butoxymethyl, 4-pentenyloxymethyl, siloxymethyl, 2-methoxyethoxymethyl, 2,2,2-trichloroethoxymethyl, bis(2-chloro- ethoxy)methyl, 2-(trimethylsilyl)ethoxymethyl, tetrahydropyranyl, 3-bromotetrahydro-pyranyl, tetrahydrothiopyranyl, 1-methoxycyclohexyl, 4-methoxytetrahydropyranyl, 4-methoxytetrahydro-thiopyranyl, 4-methoxytetraihydrothiopyranyl S,S-dioxido, 1-[(2-chloro-4-methyl)phenyl]-4-methoxypiperidin-4-yi, 1,4-dioxan-2-yi, tetrahydrofuranyl, tetra hyd rothiofu ranyl, and 2,3,3a,4,5,6,7,7a-octahydro-7,8,8-trimethyl-4,7-ethanobenzofuran-2-yl.
Substituted Ethyl Etliers Substituted ethyl ethers include: 1-ethoxyethyl, 1-(2,chloroethoxy)ethyl, 1-methyl-1-methoxyethyl, 1 --methyl-1-benzyloxyethyl, 1-methyl-1-benzyloxy-2-fluoroethyl, 2,2,2-trichloroethyl, 2-trimethylsilyethyl, 2-(phenylselenyl)ethyl, t-butyl, allyl, p-chlorophenyl, p-metlhoxyphenyl, 2,4-dinitrophenyl, and benzyl.
Substituted Benzyl E:thers Substituted benzyl ethers iriclude: p-methoxybenzyl, 3,4-dimethoxybenzyl, o-nitrobenzyl, p-nitrobenzyl, p-halobenzyl, 2,6-dichlorobenzyl, p-cyanobenzyl, p-phenylbenzyl, 2- and 4-picolyl, 3-methyl-2-picolyl N-oxido, diphenylmethyl, p, p'-dinitrobenzhydryl, 5-d i benzosu beryl, triphenylmethyl, a-naphthyl-diphenylmethyl, p-methoxyphenyldiphenylmethyl, di(p-methoxyphenyl)phenyl-methyl, tri-(p-methoxyphenyl)methyl, 4-(4'-bromophenacyloxy)phenyldiphenyl-methyl, 4,4',4"-tris(4,5-dichllorophthalimidophenyl)rnethyl, 4,41,4"-tris(levulinoyloxyphenyl) methyl, 4,4',4"tris(benzoyloxyphenyl)methyl, 3-(imidazol-1-ylmethyl)bis(4',4"-dimethoxyphenyl)-methyl, 1,1-bis(4-methoxyphenyl)-1'-pyrenylmethyl, 9-anthryl, 9-(9-phenyl) xanthenyl, 9-(9-phenyl-10-oxo) anthryl, 1,3-benzodithiolan-2-yl, and benzisothiazolyl S,S-dioxido.
Silyl Ethers Silyl ethers include: trimethylsilyl, triethylsilyl, triisopropylsilyl, dimethylisopropylsilyl, diethiylisopropylsilyi, dimethylthexylsilyl, t-butyldimethylsilyl, t-butyldiphenylsilyl, tribenzylsilyl, tri-p-xylylsilyl, triphenyisilyl, diphenylmethylsilyl, and t-butylmethoxy- phenylsilyl.

ESTERS
Esters protecting groups include: esters, carbonates, assisted cleavage, miscellaneous esters, and sulfonates.
Esters Examples of protective estiars include: formate, benzoylformate, acetate, chloroacetate, dichloroacet:ate, trichloroacetate, trifluoroacetate, methoxyacetate, triphenylmethoxyacetate, phenoxyacetate, p-chlorophenoxyacetate, p-P-phenylacetate, 3-phenylpropionate, 4-oxopentanoate (levulinate), 4,4-(ethylenedithio) pentanoate, pivaloate, adamantoate,crotonate,4-methoxycrotonate, benzoate, p-phenylbenzoate, and 2,4,6-trimethylbenzoate (mesitoate).
Carbonates Carbonates include: methyl, 9-fluorenyimethyl, ethyl, 2,2,2-trichloroethyl, 2-(trimethylsilyl) ethyl, 2-(phenylsulfonyl) ethyl, 2-(triphenylphosphonio) ethyl, isobutyl, vinyl, allyl, p-nitrophenyl, benzyl, p-methoxybenzyl, 3,4-dimethoxybenzyl, o-nitrobenzyl, p-nitrobenzyl, S-benzyl thiocarbonate, 4-ethoxy-1-naphthyl, and methyl dithiocarbonate.
Assisted Cleavage Examples of assisted cleavage protecting groups include: 2-iodobenzoate, 4-azido-butyrate, 4-nitro-4-methylpentanoate, o-(dibromomethyl) benzoate, 2-formylbenzene-sulfonate, 2-(methylthiomethoxy) ethyl carbonate, 4-(methylthiomethoxymethyl) benzoate, and 2-(methylthiomethoxymethyl) benzoate.
Miscellaneous Esters, In addition to the above classes, miscellaneous esters include: 2,6-dichloro-4-methylphenoxyacetate, 2,6-dichloro-4-(1,1,3,3-tetramethylbutyl) phenoxyacetate, 2,4-bis(1,1-dimethylpropyl) phenoxyacetate, chlorodiphenylacetate, isobutyrate, monosuccinoate, (E)-2-methyl-2-butenoate (tigloate), o-(methoxycarbonyl) benzoate, p-P-benzoate, a-naphthoate, nitrate, alkyl N,N,N',N'-tetramethyl-phosphorodiamidate, N-phenylcarbamate, borate, dimethylphosphinothioyl, and 2,4-dinitrophenylsulfenate.
Sulfonates Protective sulfates includes: sulfate, methanesulfonate(mesylate), benzylsulfonate, and tosylate.

PROTECTION FOR 12- AND 1.3-DIOLS
The protection for 1,2 and 1,3-diols group includes: cyclic acetals and ketals, cyclic ortho esters, and silyl derivatives.
Cyclic Acetals and Ketals Cyclic acetals and ketals include: methylene, ethylidene, 1-f-butylethylidene, 1-phenylethylidene, (4-methoxyphenyl) ethylidene, 2,2,2-trichloroethylidene, acetonide (isopropylidene), cyclopentylidene, cyclohexylidene, cycloheptylidene, benzylidene, p-methoxybenzylidene, 2,4-dimethoxybenzylidene, 3,4-dimethoxybenzylidene, and 2-nitrobenzyiidene.
Cyclic Ortho Esters Cyclic ortho esters include: methoxymethylene, ethoxymethylene, dimethoxy-methylene, 1-methoxyethylidene, 1-ethoxyethylidine, 1,2-dimethoxyethylidene, a-methoxybenzylidene, 1-(N,N-dimethylamino)ethylidene derivative, a-(N,N-dimethylamino) benzylidene derivative, and 2-oxacyclopentylidene.
PROTECTION FOR THE CARBOXYL GROUP
ESTERS
Ester protecting groups include: esters, substituted methyl esters, 2-substituted ethyl esters, substituted benzyl esters, silyl esters, activated esters, miscellaneous derivatives, and stannyl esters.
Substituted Methyl Esters Substituted methyl esters inciude: 9-fluorenylmethyl, methoxymethyl, methylthiomethyl, tetrahydropyranyl, tetrahydrofuranyl, methoxyethoxymethyl, 2-(trimethylsilyl)ethoxy-methyl, benzyioxymethyl, phenacyl, p-bromophenacyl, a-methylphenacyl, p-methoxyphenacyl, carboxamidomethyl, and /V
phthalimidomethyl.
2-Substituted Ethyl Esters 2-Substituted ethyl esters include: 2,2,2-trichloroethyl, 2-haloethyl, 1-chloroa0cyl, 2-(trimethylsily)ethyl, 2-methylthioethyl, 1,3-dithianyl-2-methyl, 2(p-nitrophenyl-sulfenyl)-ethyl, 2-(p-toluenesulfonyl)ethyl, 2-(2'-pyridyl)ethyl, 2-(diphenyl-phosphino)ethyl, 1-methyl-l-phenylethyl, t-butyl, cyclopentyl, cyclohexyl, allyl, 3-buten-1-yl, 4-(trimethylsily)=-2-buten-1-yl, cinnamyl, a-methylcinnamyl, phenyl, p-(methylmercapto)-phenyl, and benzyl.
Substituted Benzyl Esters Substituted benzyl esters include: triphenylmethyl, diphenylmethyl, bis(o-nitrophenyl)methyl, 9-anthrylmethyl, 2-(9,10-dioxo)anthrylmethyl, 5-dibenzo-suberyl, 1-pyrenylmethyl,2=(trifluoromethyl)-6-chromyimethyl, 2,4,6-trimethylbenzyl, p-bromobenzyl, o-nitrobenzyl, p-nitrobenzyl, p-methoxybenzyl, 2,6-dimethoxybenzyl, 4-(methylsulfinyl)benzyl, 4-sulfobenzyl, piperonyl, and 4-P-benzyl.
Silyl Esters Silyl esters include: trimethiylsilyl, triethylsilyi, t-butyldimethylsilyi, i-propyidimethylsilyl, phenyldlimethylsilyl, and di- t-butylmethylsilyl.
Miscellaneous Derivatives Miscellaneous derivatives iincludes: oxazoles, 2-alkyl-1,3-oxazolines, 4-alkyl-oxo-1,3-oxazolidines, 5-alkyl-4-oxo-1,3-dioxolanes, ortho esters, phenyl group, and pentaaminocobalt(III) complex.
Stannyl Esters Examples of stannyl esters include: triethylstannyl and tri-n-butylstannyl.
AMIDES AND HYDRAZIDES
Amides include: N,N -dimethyl, pyrrolidinyl, piperidinyl, 5,6-dihydrophenanthridinyl, o-ni itroanilides, N-7-nitroindolyl, N-8-nitro-1,2,3,4-tetrahydroquinolyl, and p-P-benzenesulfonamides. Hydrazides include: N-phenyl, N,N'-diisopropyl and other dialkyl hydrazides.
PROTECTION FOR THE AMINO GROUP
CARBAMATES
Carbamates include: carbamates, substituted ethyl, assisted cleavage, photolytic cleavage, urea-type derivatives, and miscellaneous carbamates.
Carbamates Carbamates include: methiyl and ethyl, 9-fluorenylmethyl, 9-(2-sulfo)fluorenylmethyl, 9-(2,7-dibromo)fluorenylmethyl, 2,7-di-t-butyl-[9-(10,10-dioxo-10,10,10,10-tetrahyclro- thioxanthyl)]methyl, and 4-methoxyphenacyl.

Substituted Ethyl Substituted ethyl protective groups include: 2,2,2-trichloroethyl, 2-trimethylsilyiethyl, 2-phenylethyl, 1-(1-adamantyl)-1-methyiethyl, 1,1-dimethyl-2-haloethyl, 1,1 dimethyl-2,2-dlibromoethyl, 1,1-dimethyl-2,2,2-trichloroethyl, methyl-1-(4-biphenylyl)ethyll, 1-(3,5-di-t butylphenyl)-1-methylethyl, 2-(2'-and 4'-pyridyl)ethyl, 2-(N,N-icyclohexyicarboxamido)- ethyl, t-butyl, 1-adamantyl, vinyl, allyl, 1-isopropylallyl, connamyl, 4-nitrocinnamyl, quinolyl, N-hydroxypiperidinyl, alkyldithio, benzyl, p-methoxybenzyl, p-nitrobenzyl, p-bromobenzyl, p-chloro-benzyl, 2,4-dichlorobenzyl, 4-methylsulfinylbenzyl, 9-anthrylmethyl, and diphenylmethyl.
Assisted Cleavaae Protection via assisted cleavage includes: 2-methylthioethyl, 2-methylsulfonyl-ethyl, 2-(p-toluenesulfonyl)ethyl, [2-(1,3-dithianyl)]methyl, 4-methylthiophenyl, 2,4-dimethyl-thiophenyl, 2-phosphonioethyl, 2-triphenyl-phosphonioisopropyl, 1,1=
dimethyl-2-cyanoethyl, m-clhioro-p-acyloxybenzyl, p-(dihydroxyboryl)benzyl, 5-benzisoxazolylmethyl, and 2-(trifluoromethyl)-6-chromonyimethyl.
Photolytic Cleavape Photolytic cleavage methocis use groups such as: m-nitrophenyl, 3,5-dimethoxybenzyl, o-nitrobenzyl, 3,4-dimethoxy-6-nitrobenzyl, and phenyl(o-nitrophenyl)methyl.
Urea-Type Derivatives Examples of of urea-type derivatives include: phenothiazinyl-(10)-carbonyl derivative, N'-p-toluenesulfonylaminocarbonyl, and N'-phenylaminothiocarbonyl.
Miscellaneous Carbamates In addition to the above, miscellaneous carbamates include: t-amyl, S-benzyl thiocarbamate, p-cyanoberizyl, cyclobutyl, cyclohexyl, cyclopentyl, cyclopropylmethyl, p-decyloxy-benzyl, diisopropylmethyl, 2,2-dimethoxy-carbonylvinyl, o-(N,N-dimethyi-carboxamido)-benzyl, 1,1-dimethyl-3(N,N-dimethylcarboxamido)propyl, 1,1-dimethyl-propynyl, di(2-pyridyl)methyl, 2-furanylmethyl, 2-iodoethyl, isobornyl, isobutyl, isonicotinyl, p(p'-methoxyphenyl-azo)benzyl, 1-methyicyclobutyl, 1-methylcyclohexyl, 1-methyl-1-cyclopropylmethyl, 1-methyl-(3,5-dimethoxyphenyl)ethyl, 1-methyl-1(p-henylazophenyl)- ethyl, 1-methyl-1 -phenylethyl, 1-methyl-1 -(4-pyridyl)ethyl, phenyl, p-(phenylazo)benzyl, 2,4,6-tri-t-butylphenyl, 4-(trimethylammonium)-benzyl, and 2,4,6-trimethylbenzyl.
AMIDES
Amides Amides includes: N-formyl, N-acetyl, N-chloroacetyl, N-trichloroacetyl, N-trifluoroacetyl, N-phenylacetyl, N-3-phenylpropionyl, N-picolinoyl, N-3-pyridyl-carboxamide, N-benzoylphenylalanyl derivative, N-benzoyl, and N-p-phenylbenzoyl.
Assisted Cleavage Assisted cleavage groups iriclude: N-o-nitrophenylacetyl, N-o-nitrophenoxyacetyl, N-acetoacetyl, (N'-dithiobenzyloxycarbonylamino)acetyl, N-(p-hydroxphenyl) propionyl, N-3-(o-nitrophenyl)propionyl, N-2-methyl-2-(o-nitrophenoxy)propionyl, N-2-methyl-2-(o-phenylazophenoxy)propionyl, N-4-chlorobutyryl, N-3-methyl-3-nitrobutyryl, N-o-nitrocinnamoyl, N-acetylmethionine derivative, N-o-nitrobenzoyl, N-o-(benzoyloxymethyl)benzoyl, and 4,5-diphenyl-oxazolin-2-one.
Cyclic Imide Derivatives Cyclic imide derivatives include: N-phthalimide, N-dithiasuccinoyl, N-2,3-diphenyi-maleoyl, N-2,5-dimethylpyrrolyl, N-1,1,4,4-tetramethyl-disilylazacyclopentane adduct, 5-substituted 1,3-dimethyl-1,3,5-triazacyclohexan-2-one, 5-substituted 1,3-dibenzyl-1,3,5-triazacyclohexan-2-onie, and 1-substituted 3,5-dinitro-4-pyridonyl.
SPECIAL -NH PROTECTIV'E GROUPS

Protective groups for - NH include: N-alkyl and N-aryl amines, imine derivatives, enamine derivatives, and N-hetero atom derivatives (such as N-metal, N-N, N-P, N-Si, and N-S), N-sulfenyl, and N-sulfonyl.

N-Alkyl and IV Aryl Arnines N-alkyl and N-aryl amines include: N-methyl, N-allyl, N-[2-(trimethylsilyl)ethoxyl]-methyl, N-3-acetoxypropyl, N-(1-isopropyl-4-nitro-2-oxo-3-pyrrolin-3-yl), quaternary ammonium salts, N-benzyl, N-di(4-methoxyphenyl)methyl, N-5-dibenzosuberyl, N-triphenylmethyl, N-(4-methoxyphenyl)diphenylmethyl, N-9-phenylfluorenyl, N-2,7-cl ichloro-9-fluorenylmethylene, N-ferrocenylmethyl, and N-2-picolylamine N'-oxiide.
Imine Derivatives lmine derivatives include: N-1,1-dimethylthiomethylene, N-benzylidene, N-p-methoxybenzylidene, N-diphenylmethylene, N-[(2-pyridyl)mesityl]methylene, N-(N',N'-dimethyiaminomeithylene), N,N'-isopropylidene, N-p-nitrobenzylidene, N-salicylidene, IV 5-chlorosailicylidene, N-(5-chloro-2-hydroxyphenyl)-phenylmethylene, and N-cyclohexylidene.
Enamine Derivative An example of an enamine derivative is N-(5,5-dimethyl-3-oxo-l-cyclohexenyl).
N-Hetero Atom Derivatives N-metal derivatives include: N-borane derivatives, N-diphenylborinic acid derivative, N-[phenyl(pentacarbonylchromium- or -tungsten)]carbenyl, and N-copper or N-zinc chelate. Examples of N-N derivatives include: N-nitro, N-nitroso, and N-oxide. Examples of N-P derivatives include:
N-diphenylphosphinyl, N-dirnethylthiophosphinyl, /V diphenylthiophosphinyl, N-dialkyl phosphoryl, N-dibenzyl phosphoryl, and N-diphenyl phosphoryl.
Examples of N-sulfenyl derivatives include: N-benzenesulfenyl, N-o-nitrobenzenesulfenyl, N-2,4-dinitrobenzenesulfenyl, N-pentachlorobenzene-sulfenyl, N-2-nitro-4-methoacy-benzenesulfenyl, N-triphenylmethylsulfenyl, and N-3-nitropyridinesulfenyl. N-sulfonyl derivatives include: N-p-toluenesulfonyl, N-benzenesulfonyl, N-2,3,6-trimethyl- 4-methoxybenzenesulfonyl, N-2,4,6-trimethoxybenzenesulifonyl, N-2,6-dimethyl-4-methoxy-benzenesulfonyl, N-pentamethylbenzenesulfonyl, N-2,3,5,6-tetramethyl-4-methoxybenzene- sulfonyl, N-4-methoxybenzenesulfonyl, N-2,4,6-trimethylbenzenesulfonyl, N-2,6-dimethoxy- 4-methylberizenesulfonyl, N-2,2,5,7,8-pentamethyl-chroman-6-sulfonyl, N-methanesulfonyl, N-,l3-trimethylsilylethanesulfonyl, N-9-anthracenesulfonyl, N-4-(4',8'-dimethoxynaphthylmethyl)-benzenesulfonyl, N-benzylsulfonyl, N-trifluoromethylsulfonyl, and N-phenacylsulfonyl.

Disclosed compounds which are masked or protected may be prodrugs, compounds metabolized or otherwise transformed in vivo to yield a disclosed compound, e.g., transiently during metabolism. This transformation may be a hydrolysis or oxidation which results from contact with a bodily fluid such as blood, or the action of acids, or liver, gastrointestinal, or other enzymes.
Features of the invention are further described in the examples below.
E. EXAMPLES

Preparation of 7-fluoro-6-(4-iodo-2-methyl-phenyiamino)-1 H-benzoimidazole-5-carboxylic acid (PD 205293) (APK IC50 = 14 nM; colon 26 cells, IC50 => 10 micromolar) Step a: Preparation of 5-nitro-2 3 4-trifluorobenzoic acid To gently stirring concentrated sulfuric acid (50 ml) was added fuming nitric acid (3.4 ml, 0.076 mol). Solid 2,3,4-trifluorobenzoic acid (10.00 g, 0.05565 mol) was added directly in increments. After stirring 45 minutes, the reaction mixture had become an orange homogeneous solution which was then poured over chilled water (400 mi). The resulting aqueous suspension was extracted with diethyl ether (3 x 200 ml). The combined extracts were dried with anhydrous magnesium sulfate and concentrated in vacuo to yield 12.30 g of a dull, light-yellow solid. Recrystallization from chloroform (50 mi) afforded 9.54 g of the pale yellow microcrystalline product; 78 % yield; m.p. ;' H-NMR (400 MHz; DMSO) S
14.29 (broad s, 1H), 8.43-8.:38 (m, 1H); 13C-NMR (100 MHz; DMSO) S 162.41, 154.24 (dd, JC.F=270.1, 10.7 Hz), 148.35 (dd, JC_F=267.0, 9.2 Hz), 141.23 (dt, Jc_ F=253.4 Hz), 133.95, 123.30, (d, JC_F=2.2 Hz), 116.92 (dd, Jc_F=18.2, 3.8 Hz);

NMR (376 MHz; DMSO) S -1120.50 to -120.63 (m), -131.133 to -131.27 (m), -153.63 to -153.74 (m).

Step b: Preparation of 4-amino-2.3-difluoro-5-nitrobenzoic acid Solid 5-nitro-2,3,4-trifluorobenzoic acid (0.75 g, 0.00339 mol) was dissolved in concentrated animonium hydroxide (25 ml) to give instantly a yellow solution. A precipitate began to form within five minutes, after which time the mixture was acidified to pH 0 with concentrated aqueous hydrochloric acid. A
yellow precipitate rapidly forrned. The mixture was heated to boiling and was filtered hot. The yellow solids were washed with 10 % aqueous hydrochloric acid and were suction dried to afford 0.47 g of a yellow powder; 64 % yield;'H-NMR
(400 MHz; DMSO) S 13.32 (s, 1 H), 8.36 (d, 1 H, J=7.6 Hz), 7.98 (s, 2H); 19F-NMR
(376 MHz; DMSO) S -128.69 to -128.76 (m), -153.60 (d).

Step c: Preparation of ineth I 4-amino-2,3-difluoro-5-nitrobenzoate Hydrogen chloride gas was dissolved-in anhydrous methanol (30 ml) until the solution was warm. The solid 4-amino-2,3-difluoro-5-nitrobenzoic acid (0.47 g; 0.00215 mol) was dissolved in this solution and the reaction mixture was brought to reflux with vigorous stirring for 23 hours under a nitrogen atmosphere.
The reaction mixture was allowed to cool slowly on the bench. A yellow precipitate formed and was collected by vacuum filtration and dried with suction to afford 0.35 g of yellow microfilaments; 70 % yield; m.p. 183.5-184 C; 'H-NMR
(400 MHz; DMSO) S 8.36 (did, 1 H, J=7.3, 1.7 Hz), 8.06 (s, 2H), 3.78 (s, 3H);

NMR (376 MHz; DMSO) S-1128.85 to -128.92 (m), -153.29 (d); MS (APCI-) 231 (M-1, 100); IR (KBr) 3433, 3322, 1700, 1650, 1549, 1343, 1285 cm"1; Anal.
calcd/found for: C8HsF2N204 C, 41.39/41.40; H, 2.61/2.50; N, 12.07/11.98; F, 16.37/16.58.

Step d: Preparation of inethyl 4-amino-3-fluoro-2-(2-methvl-phenylamino)-5-nitrobenzoate The solid methyl 4-annino-2,3-difluoro-5-nitrobenzoate (0.087 g, 3.7 x 10-4 mol) was dissolved in ortho-toluidine (3 ml, 0.028 mol). The reaction mixture was stirred at 200 C for 35 minutes under a nitrogen atmosphere. The mixture was then partitioned between diethyl ether (150 ml) and 10 % aqueous hydrochloric acid (150 ml). The ether phase was dried with anhydrous magnesium sulfate and was concentrated in vacuo to a crude solid. The crude product was dissolved in ml of dichloromethane anci was filtered through a flash silica plug. Elution with 5 dichloromethane afforded 0.0953 g of a yellow solid; 81 % yield; m.p. 164-168 C;
1H-NMR (400 MHz; DMSO) S 9.20 (s, 1 H), 8.52 (d, 1 H, J=1.7 Hz), 7.57 (s, 2H), 7.19 (d, 1 H, J=7.3 Hz), 7.12-7.08 (m, 1 H), 7.02-6.98 (m, 1 H), 6.95-6.91 (m, 1 H), 3.78 (s, 3H), 2.21 (s, 3H);191F-NMR (376 MHz; DMSO) 8 -141.13 (s); MS (APCI+) 320 (M+1, 100); (APCI-) 318 (M-1, 100); IR (KBr) 3467, 3346, 1690, 1305 cm"';
Anal. calcd/found for: C15HuFN304 '0.21 H20 C, 55.77/55.97; H, 4.50/4.55; N, 13.01/12.61; F, 5.88/5.95.

Step e: Preparation of inethi/l 4,5-diamino-3-fluoro-2-(2-methyl-phenyiamino)benzoate To a mixture comprisied of methyl 4-amino-3-fluoro-2-(2-methyl-phenylamino)-5-nitrobenzoate (2.52 g, 0.00789 mol), tetrahydrofuran (50 ml), methanol (50 ml) and washed Raney nickel (0.5 g) was initially applied 48.6 psi of hydrogen gas at 30.2 C in a shaker for 4 hours 48 minutes. The mixture was filtered and the filtrate concentrated in vacuo to afford 2.20 g of a salmon-colored amorphous solid; 96 % yield; ' H-NMR (400 MHz; DMSO) S 7.84 (s, 1 H), 7.04 (d, 1 H, J=7.1 Hz), 6.98 (d, 1 H, J=1.2 Hz), 6.95-6.91 (m, 1 H), 6.68-6.64 (m, 1 H), 6.40-6.36 (m, 1 H), 5.39 (s, 2H), 4.73 (s, 2H), 3.66 (s, 3H), 2.21 (s, 3H); 19F-NMR
(376 MHz; DMSO) S -139.66 (s).

Step f: Preparation of inethyl 7-fluoro-6-(2-methyl-phenylamino -benzoimidazole-5-carboxylate A stirring solution connprised of methyl 4,5-diamino-3-fluoro-2-(2-methyl-phenylamino)-benzoate (1.78 g, 0.00615 mol) in formic acid (Aldrich, 95-97 %, 100 ml, 2.5 mol) was brougtit to reflux for 3 hours followed by concentration in vacuo to give a crude browni solid. The crude product was triturated with chloroform (40 ml) and subsequently collected by vacuum filtration. The solids were dried with suction to aiford 1.09 g of a light-lavender powder. The filtrate was concentrated in vacuo to a crude solid which was triturated with 10 ml of chloroform-dichloromethane. These solids were collected by vacuum filtration, rinsed with dichforomethane, and were suction-dried to give an additional 0.55 g of a light-lavender powder (total yield: 1.64 g); 87 % yield; m.p. 259-262 C;

NMR (400 MHz; DMSO) S 8.42 (s, 1 H), 8.03 (s, 1 H), 7.93 (broad s, 1 H), 7.12 (d, 1 H, J=7.0 Hz), 6.99-6.95 (m, 1 H), 6.75-6.71 (m, 1 H), 6.48-6.44 (m, 1 H), 3.81 (s, 3H), 2.30 (s, 3H); 19F-NMR (376 MHz; DMSO) 8 -132.84 (s); MS (APCI+) 300 (M+1, 100); (APCI-) 298 (M-1, 100); IR (KBr) 3322, 1689, 1437, 1326, 1218 cm',;
Anal. calcd/found for: C16H1,4FN302 -0.32 H20 C, 62.99/63.01; H, 4.84/4.61; N, 13.77/13.70.

Step g: Preparation of methyl 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzoimidazole-5-carboxylate A stirring mixture connprised of methyl 7-fluoro-6-(2-methyl-phenylamino)-1 H-benzoimidazole-5-carboxylate (0.2492 g, 8.326 x 10'4 mol), benzyltrimethylammonium clichloroiodinate (Aldrich, 95 %, 0.3934 g, 0.00113 mol), and zinc chloride (0.1899 g, 0.00139 mol) in glacial acetic acid (20 ml) was brought to reflux for 15 minutes. The hot suspension was filtered to isolate the precipitate which was dried in the vacuum oven (90 C, ca. 10 mm Hg) overnight to afford 0.2392 g of a green powder; 68 % yield; m.p. 219-220 C DEC; 'H-NMR
(400 MHz; DMSO) S 8.71 (s, 1 H), 8.02 (s, 1 H), 7.85 (broad s, 1 H), 7.43 (d, 1 H, J=1.7 Hz), 7.24 (dd, 1 H, J=8.5, 2.2 Hz), 6.24 (dd, 1 H, J=8.5, 5.4 Hz), 3.76 (s, 3H), 2.22 (s, 3H);'9F-NMR (376 MHz; DMSO) 8 -132.86 (s); MS (APCI+) 426 (M+1, 48), 169 (100); (APCI-) 424 (M-1, 100); IR (KBr) 1704, 1508, 1227 cm 1.
Step h: Preparation of 7-fluoro-6-(4-iodo-2-methvl-phenvlamino)-1 H-benzoimidazole-5-carboxylic acid To a stirring solution comprised of methyl 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzoimidazole-5-carboxylate (0.2035 g, 4.786 x 104 mol) in tetrahydrofuran (20 ml) was added solid potassium trimethylsilanolate (0.315 g, 0.00246 mol). The reaction mixture was stirred at ambient temperature under argon for 16 hours. An additional 0.082 g (6.39 x 10-4mol) of potassium trimethylsilanolate was added and the mixture stirred 30 minutes. The reaction mixture was concentrated in vacuo to one-third volume and was treated with diethyl ether (50 ml). The off white precipitate formed was collected by vacuum filtration, giving a hygroscopic solid. The wet solid was dissolved in a 4:1 (v/v) ethyl acetate-methanol solution (500 ml). The solution was washed with 0.84 M
aqueous citric acid (50 ml), ciried (MgSO4), and concentrated in vacuo to a yellow liquid. The liquid was redissolved in fresh ethyl acetate-methanol. The solution was washed with brine, dried (MgSO4), and concentrated in vacuo. The residue was redissolved in chlorofonrn and reconcentrated to afford 1.55 g of a viscous yellow residue which was comprised mainly of citric acid; MS (APCI-) 191 (M-1, 100). The residue was dissolved in water (50 ml). Insoluble material was extracted into 1:1 (v/v) ethyl acetate-diethyl ether (250 ml). Upon separation, the aqueous phase remained stirongly acidic (pH 0). The organic phase was washed with a fresh portion of water (150 ml). Upon separation, this wash was only slightly acidic (pH 4.5). The organic phase was dried (MgSO4), concentrated in vacuo, and chased with chloroform to give a tan semisolid. The product was triturated with hexanes. Vacuum filtration and suction-drying afforded 0.0839 g of a tan powder. A portion of the product (0.050 g) was recrystallized from boiling ethanol (1 ml). While coofing and moderate scratching, an off-white solid formed.
This product was isolated by vacuum filtration and dried under high vacuum (23 C) to afford 0.018 g of an oiff-white powder; 9 % yield; m.p. 247-248 C DEC;
'9F-NMR (376 MHz; DMSO) & -132.87 (s); MS (APCI+) 412 (M+1, 100); (APCI-) 410 (M-1, 100); IR (KBr) 3322, 1689, 1437, 1326, 1218 cm"1; Anal. calcd/found for: C75HliFIN3O2 '0.61 C2H,g0 ' 0.59 H20 (91.4 % parent) C, 43.30/43.30; H, 3.55/3.34; N, 9.34/9.15.

Preparation of 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzoimidazole-5-carboxylic acid cyclopropylmethoxy-amide (PD 254552) (APK IC50 < 10 nM

(n = 2); colon 26 cells, 1 hour pretreatment, IC50 = 20 nM) Step a: Preparation of 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzoimidazole-5-carboxylic: acid pentafluorophenyi ester (PD 254551) (APK ICo = 120 nM (n=2)) To a stirring suspension comprised of 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzoimidazole-5-carboxylic acid (0.844 g, 2.05x10"3 mol) in ethyl acetate (4 ml) was added a solution comprised of pentafluorophenol (0.375 g, 2.04x10"3 mol) in N,N-dimethylformamide (10 ml). Solid dicyclohexylcarbo-diimide (0.415 g, 1.99x10"3 rnol) was then added and the reaction mixture was stirred for 22 hours. The reaction mixture was vacuum filtered to remove the precipitate that had formed. The flltrate was diluted with ethyl acetate (400 ml), and that solution was washed with water (3x400 ml), was dried (MgSO4), and was concentrated in vacuo to afford 1.7 g of a yellow foam. The crude product was purified by flash silica column chromatography. Elution with a gradient (CHCI3 to 0.5 % methanol in CHCI3) afforded 0.69 g of the yellow amorphous product; 60 % yield; 1H-NMR (400 MHz; CDCI3) S 8.54 (s, 1 H), 8.28 (s, 1 H), 8.04 (s, 1 H), 7.49 (d, 1 H, J=1.7 Hlz), 7.36 (dd, 1 H, J=8.2, 1.7 Hz), 6.57 (dd, 1 H, J=8.4, 6.5 Hz), 2.31 (s, 3H); '9F-NMR (376 MHz; CDCI3) 8 -132.02 (s), -152.35 (d, J=18.3 Hz), -157.26 (t, J=21.4 Hz), -161.96 (dd, J=21.3, 18.3 Hz); MS (APCI+) 578 (M+1, 57), 394 (100); (APCI-) 576 (M-1, 44), 409 (100), 393 (95), 392 (82), 378 (55), 183 (97), 165 (68), 127 (53); IR (KBr) 1731 cm"' (C=0 stretch).

Step b: Preparation of 7-fluoro-6-(4-iodo-2-methv!-ahenylamino)-1 H-benzoimidazole-5-carboxylic: acid cyclooropylmethoxv-amide To a stirring solution comprised of 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzoimidlazole-5-carboxylic acid pentafluorophenyl ester (0.63 g, 1.09x10"3 mol) in anhydrous tetrahydrofuran (5 ml) was added solid cyclopropylmethoxylamine hydrochloride (0.14 g, 1.13x10"3 mol) and diisopropylethylamine (0.6 mi, 3.4x10'3 mol). The reaction mixture was stirred for one week. The solvent was removed and the evaporate was treated with 10 %

aqueous hydrochloric acid (200 ml) and was extracted with diethyl ether (200 ml).
A biphasic suspension resulted, and the precipitate was isolated by vacuum filtration. The crude product was recrystallized from absolute ethanol to afford 0.18 g of a green-yellow povrder; 35 % yield; mp 168-172 C; ' H-NMR (400 MHz;
DMSO) S 11.48 (s, 1 H), 8.37' (s, 1 H), 7.50 (broad s, 1 H), 7.45 (s, 1 H), 7.24 (s, 1 H), 7.07 (d, 1 H, J=8.4 Hz), 6.03-5.97 (m, 'I H), 3.38 (d, 2H, J=6.5 Hz), 2.04 (s, 3H), 0.85-0.75 (m, 1 H), 0.30-0.22 (m, 2H), 0.00 (s, 2H); 19F-NMR (376 MHz;
DMSO) 8 -133.23 (s); MS (APCI+) 481 (M+1, 77), 409 (100); (APCI-) 480 (M, 22), 407 (100); IR (KBr) 1659, 1632, 1493 cm-'; Anal. calcd/found for:
C19H18FIN4O2' 0.50 HCI (96.3 % parent) C, 45.78/45.74; H, 3.74/3.84; N, 11.24/10.88.

Pregaration of 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzoimidazole-5-carboxylic acid hydroxyamide Step a: Preparation of 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzoimidazole-5-carboxylic: acid O-(tetrahvdro-2H-pyran-2-vl)-oxyamide A solution comprised of 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzoimidazole-5-carboxylic; acid, O-(tetrahydro-2H-pyran-2-yl)-hydroxylamine (1.25 equiv.), benzotriazole-l-yl-oxy-tris-pyrrolidino-phosphonium hexafluorophosphate (1.25 equiv.), and diisopropylethylamine (3 equiv.) in 1:1 v/v tetrahydrofuran-dichloromethane is stirred for 30 minutes. The reaction mixture is concentrated in vacuo and the residue is purified by flash chromatography;
elution with dichloromethane affords the desired product. The product may be recrystallized with an appropriate solvent like methanol if further purification is necessary.

Step b: Preparation of 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzoimidazole-5-carboxylic acid hydroxyamide The compound 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzoimidazole-5-carboxylic acid O-(tetrahydro-2H-pyran-2-yl)-oxyamide is dissolved in an appropriate hiydrogen chloride-saturated solvent like methanol or ethanol. Once homogeneous, the solution is concentrated in vacuo to give the desired product. The product may be triturated with an appropriate solvent like chloroform or dichloromethane if further purification is necessary.

Preparation of 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzoimidazole-5-carboxylic acid cyclopropvlmethoxv-amide Step a: Preparation of O-cyclopropylmethylhydroxylamine hydrochloride Step i: Preparation of 2-cvlc)propylmethoxv-isoindole-1,3-dione To a stirring solution/suspension comprised of N-hydroxyphthalimide (Aldrich, 57.15 g, 339.8 mmol), cyclopropanemethanol (Aldrich, 25.10 g, 341.1 mmol), and triphenylphosphine ("DEAD," Aldrich, 91.0 g, 344 mmol) in 1.00 L of tetrahydrofuran under a nitrogen atmosphere and cooled to 6 C (internal mixture temperature) with an ice-water bath was added diethyl azodicarboxylate (Aldrich, 56 ml, 356 mmol) dropwise over 20 minutes via addition funnel. The reaction mixture temperature was kept below 20 C during the addition. Following addition of the DEAD, the cold bath was removed and the reaction mixture was stirred for 15 hours. The mixture was concentrated to a paste under reduced pressure. Chloroform (ca. 300 ml) was added and the mixture swirled to loosen all solids. Vacuum filtration iremoved the insolubles. The filtrate was likewise filtered to remove white precipitate that formed and to give a clear filtrate.
Concentration under reduced pressure afforded a clear oil. Flash filtration through silica gel (100 % chloroform) gave filtrates containing unseparated product. These filtrates were combined and concentrated under reduced pressure to afford 127.4 g of a clear oil. The oil was dissoived in absolute ethanol (400 ml) and the solution was refrigerated for two hours. A white crystalline solid had precipitated and was subsequently collected by vacuum filtration. The product was dried in the vacuum oven (60 C) to afford 42.66 g (58 %) of the desired material; m.p. 71-77 C;'H-NMR (400 MHz; CDCI3 signal offset to S
6.96) S 7.54-7.43 (m, 4H), 3.74 (d, 2H, J=7.6 Hz), 1.02-0.95 (m, 1 H), 0.34-0.30 (m, 1 H), 0.04-0.00 (m, 1 H).
Step ii: Preaaration of O-cycloproavlmethylhydroxylamine hydrochloride To a stirring solution comprised of 2-cyclopropylmethoxy-isoindole-1,3-dione (42.64 g, 196.3 mmol) in 150 ml of dichloromethane under ambient conditions was carefully added methylhydrazine (Aldrich, 10.7 ml, 197 mmol). A white precipitate began to form alrnost instantly. After 15 minutes of vigorous stirring, the suspension was vacuum filtered. The filtrate was likewise filtered to remove additional precipitate. The resulting clear filtrate was concentrated carefully (volatile product) under reduced pressure to afford a clear liquid/solid mixture.
The white solids were removed when an ether (200 ml) solution of the product was made and vacuum filtered. The filtrate was acidified with gaseous hydrogen chloride, affording instantly a white precipitate. Collection of the solid by vacuum filtration and vacuum-oven drying (55 C) afforded 18.7 g (77 %) of the white powder product; m.p. 165-168 C; 'H-NMR (400 MHz; DMSO) 8 10.77 (broad s, 2H), 3.57 (d, 2H, J=7.3 Hz), 0.84-0.74 (m, 1 H), 0.31-0.25 (m, 2H), 0.04-0.00 (m, 1 H); 13C-NMR (100 MHz; DMSO) S 75.39, 5.52, 0.00.

Step b: Preparation of 7-fluoro-6-L4-iodo-2-methyl-phenylamino)-1 H-benzoimidazole-5-carboxvlic acid cyclopropylmethoxy-amide A solution comprised of 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzoimidazole-5-carboxylic acid, O-cyclopropylmethylhydroxylamine hydrochloride (1.25 equiv.), benzotriazole-1-yl-oxy-tris-pyrrolidino-phosphonium hexafluorophosphate (1.25 equiv.), and diisopropylethylamine (3 equiv.) in 1:1 v/v tetra hyd rofuran-d ichloromettiane. is stirred for 30 minutes. The reaction mixture is concentrated in vacuo and ttie residue is taken up into diethyl ether. The ether phase is washed with dilute aqueous hydrochloric acid, saturated aqueous sodium bicarbonate, and brine, is dried (MgSO4), and is concentrated in vacuo to afford the desired product. The product may be recrystallized with an appropriate solvent like methanol or chloroform if further purification is necessary.

Preparation of 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzooxazole-5-carboxylic acid Step a: Preparation of 5-nitro-2.3,4-trifluorobenzoic acid Same as for Example 1, Step a.

Step b: Preparation of 2,3-difluoro-4-hydroxy-5-nitrobenzoic acid The solid 5-nitro-2,3,4-trifluorobenzoic acid (1.00 g, 0.00452 mol) was dissolved in 10 wt. % aqueous sodium hydroxide solution. The mixture was clear deep orange. After standing under ambient conditions for several minutes, the mixture was quenched with concentrated aqueous hydrochloric acid until strongly acidic (pH 0). A white solid precipitated which was isolated by vacuum filtration and dried with suction to afiFord 0.40 g of an off-white solid. This solid was recrystallized from chloroform (20 ml) to afford 0.22 g of an off-white crystalline powder; 22 % yield; MS (APCI-) 218 (M-1, 100).

Step c: Preparation of inethyl 2,3-difluoro-4-hydroxv-5-nitrobenzoate Anhydrous hydrogeri chloride gas was dissolved in anhydrous methanol (50 ml) until the solution wais warm. The microcrystalline solid 2,3-difluoro-hydroxy-5-nitrobenzoic acici 0.22 g, 0.00100 moi) was dissolved in the methanolic hydrogen chloride solution. The stirring reaction mixture was brought to reflux under nitrogen for 16 hours. The mixture was concentrated in vacuo to give a white solid. The product was dried under high vacuum to afford 0.213 g of a white powder; 91 % yield; rn.p. 108-109.5 C; ' H-NMR (400 MHz; DMSO) 8 8.25 (dd, 1 H, J=7.7, 2.2 Hz), 3.83 (s, 3H); (CDCI3) S 10.83 (s, 1 H), 8.66 (dd, 1 H, J=7.0, 2.2 Hz), 3.98 (s, 3H); 19F-NMR (376 MHz; DMSO) 5-127.85 (s), -154.32 (d, J=19.8 Hz); (CDCI3) 8-118.31 to -118.37 (m), -152.38 (d, J=18.3 Hz); MS (APCI-) 232 (M-1, 100); IR (KBr) 3264, 1731, 1640, 1546, 1307, 1286, 1160 cm"'.

Step d: Preparation of 1-adamantyl 4-carboxvmethvl-2,3-difluoro-6-nitrophenyl carbonate To a solution comprised of 1-adamantyl fluoroformate (2.0 M) and pyridine (2.0 M) in tetrahydrofurars is added a stirred solution comprised of methyl 2,3-difluoro-4-hydroxy-5-nitrobenzoate (0.96 equiv., 0.384 M) in anhydrous tetrahydrofuran at ambient temperature. The reaction mixture is stirred for 6 hours and the solvent is removed in vacuo. The residue is dissolved in dichloromethane. The organic solution is washed with dilute aqueous hydrochloric acid, dilute aiqueous sodium carbonate, and water, is dried (MgSO4), and is concentrated in vacuo to give the desired product.
Step e: Preparation of 1-adamantyl 4-carboxymethyl-2-fluoro-3-(2-methvl-phenylamino)-6-nitropheniyl carbonate The compound 1-aidamantyl 4-carboxymethyl-2,3-difluoro-6-nitrophenyl carbonate is dissolved in excess ortho-toluidine. The reaction mixture is stirred at 200 C for 6 hours. The nnixture is allowed to cool and is dissolved in diethyl ether. The organic phase is washed with dilute aqueous hydrochloric acid, saturated aqueous sodiunn bicarbonate, and brine, is dried (MgSO4), and is concentrated in vacuo to afford the desired product. The product is purified by flash chromatography as necessary.
Step f: Preparation of methyl 3-fluoro-4-hvdroxy-2-(2-methyl-ahenvlamino)-5-nitrobenzoate The compound 1-adamantyl 4-carboxymethyl-2-fluoro-3-(2-methyl-phenylamino)-6-nitrophenyl carbonate is dissolved in excess trifluoroacetic acid at ambient temperature. The mixture is stirred for 20 minutes. The TFA is removed under reduced pressure. The residue is subjected to vacuum pump to remove adamantan-l-ol to give the desired product.

Step g: Preparation of inethyl 5-amino-3-fluoro-4-hydroxy-2-(2-methyl-ehenyiamino)-benzoate The compound miethyl 3-fluoro-4-hydroxy-2-(2-methyl-phenylamino)-5-nitrobenzoate is treated as in Step e, Example 1.

Step h: Preparation of rnethyl 7-fluoro-6-(2-methyl-phenylamino)-1 H-benzooxazole-5-carboxt I~ ate The compound 5=-amino-3-fluoro-4-hydroxy-2-(2-methyl-phenylamino)-benzoate is treated as iri Step f, Example 1. The product may be recrystallized with an appropriate solvent like chloroform or ethanol if further purification is necessary.
Step i: Preparation of methyl 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzooxazole-5-carbo)oi/ ate A stirring mixture comprised of methyl 7-fluoro-6-(2-methyl-phenylamino)-1 H-benzooxazole-5-carboxylate (0.042 M), benzyltrimethylammonium dichloroiodinate (Aldrichi, 95 %, 0.057 M, 1.36 equiv.), and zinc chloride (0.070 M, 1.67 equiv.) in glacial acetic acid is brought to reflux for 15 minutes. The mixture is concentrated in vacuo and the residue taken up into diethyl ether. The ether solution is washed with dilute aqueous hydrochloric acid, water, and brine, is dried (MgSOa), and is concentrated in vacuo to obtain the desired product. The product may be purified by recrystallization with an appropriate solvent like ethanol.

Step j: Preparation of 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzooxazole-5-carbox,liy c acid To a stirring solution comprised of methyl 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzooxazole-5-carboxylate (0.024 M) in tetrahydrofuran is added solid potassium trimethylsilanolate (5.14 equiv.). The reaction mixture is stirred at ambient temperatiure under argon for 16 hours. An additional equivalent of potassium trimethylsilanolate is added and the mixture stirred 30 minutes.
The reaction mixture is concentrated in vacuo to give a residue that is then taken up into 1:1 (v/v) ethyl acetate-ciiethyl ether. The organic phase is washed with dilute aqueous hydrochloric acid, water, and brine, is dried (MgSO4), is concentrated in vacuo, and chased with chloroform to give a crude product. Recrystallization from an appropriate solvenl: like ethanol gives the purified desired product.

Preparation of 7-fluoro-6-(4-iodo-2-methyl-phenYlamino)-1 H-benzooxazole-5-carboxvlic acid hydroxyamide Step a: Preparation of 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzooxazole-5-carboxvlic acid O-(tetrahydro-2H-pyran-2-yl)-oxyamide The compound 7-fluoro-6-(4-iodo-2-methyl-pheny{amino)-1 H-benzooxazole-5-carboxylic acid is treated as in Step a, Example 2.
Step b: Preparation of 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzooxazole-5-carboxylic acid hydroxyamide The compound 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzooxazole-5-carboxylic acid O-(tetrahydro-2H-pyran-2-yl)-oxyamide is treated as in Step b, Example 2.

Preparation of 7-fluoro-6-(4-iodo-2-methvl-phenylamino)-1 H-benzooxazole-5-carboxylic acid cyclopropyfinethoxy-amide The compound 7-flu,oro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzooxazole-5-carboxylic acid is treated as in Step b, Example 3.

Preparation of 7-fluoro-6-f4-iodo-2-methyl-phenYlamino)-1 H-benzothiazole-5-carboxvlic acid Step a: Preparation of 5-nitro-2 3 4-trifluorobenzoic acid Same as for Example 1, Step a.

Step b: Preparation of 2,3-difluoro-4-hvdroxy-5-nitrobenzoic acid Same as for Example 4, Step b.

Step c: Preparation of methyl 2,3-difluoro-4-hydroxy-5-nitrobenzoate Same as for Example 4, Step c.

Step d: Preparation of 4-dimethylthiocarbamoyloxy-2,3-difluoro-5-nitro-benzoic acid methyl ester A solution of methyl 2,3-difluoro-4-hydroxy-5-nitrobenzoate in N,N-dimethylformamide is treated with one molar equivalent of cesium carbonate and warmed to 85 C for 30 minutes. The stirring mixture is then treated dropwise rapidly with a solution coniprised of a slight excess of N,N-dimethylthiocarbamoyl chloride in N,N-dimethylformamide. The reaction mixture is stirred at room temperature for one hour, or may be warmed over a steam bath for one hour.
The mixture is then poured into water and extracted with ethyl acetate. The organic phase is washed with 5 % aqueous sodium hydroxide, water, and brine, and is then dried with a diying agent like magnesium sulfate of sodium sulfate.
The solvent is then removed in vacuo to give a crude product. The compound is purified by ordinary methods such as chromatography or crystallization from an appropriate solvent.

Step e: Preparation of 4-Dimethylthiocarbamoyloxy-3-fluoro-5-nitro-2-o-tolylamino-benzoic acid niethyl ester The compound 4-dirnethylthiocarbamoyloxy-2,3-difluoro-5-nitro-benzoic acid methyl ester is dissolved in excess o-toluidine. The stirring mixture is brought to 200 C for one hour. The mixture is then poured into 5 % aqueous hydrochloric acid. The aqueous mixture is extracted with diethyl ether. The organic phase is washed with water and brine, is dried over magnesium sulfate, and is concentrated in vacuo. The crude product is purified by ordinary methods such as chromatography or crystallization from an appropriate solvent.

Step f: Preparation of methyl 7-fluoro-6-(2-methyl-phenylamino)-1 H-benzothiazole-5-carboxylate The compound methyl 5-amino-3-fluoro-4-mercapto-2-(2-methyl-phenylamino)-benzoate is treated as in Step h, Example 4.

Step g: Preparation of inettyl 7-fluoro-6-(4-iodo-2-methvl-phenylamino)-1 H-benzothiazole-5-carboxylate The compound mettiyl 7-fluoro-6-(2-methyl-phenylamino)-1 H-benzothiazole-5-carboxylate is treated as in Step i, Example 4.

Step h: Preparation of 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzothiazole-5-carboxvlic acid The compound methyl 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzothiazole-5-carboxylat:e is treated as in Step j, Exampie 4.

Preparation of 7-fluoro-6-(4-iodo-2-methvl-phenvlaminol-1 H-benzothiazole-5-carboxylic acid hydroxyamide Step a: Preparation of 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzothiazole-5-carboxylic acid O-(tetrahydro-2H-)vran-2-vl)-oxyamide The compound 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzothiazole-5-carboxylic: acid is treated as in Step a, Example 2.

Step b: Preparation of 7-fluoro-6-(4-iodo-2-methvl-phenvlamino)-1 H-benzothiazole-5-carboxylic acid hydroxyamide The compound 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzothiazole-5-carboxylic acid O-(tetrahydro-2H-pyran-2-yl)-oxyamide is treated as in Step b, Example 2.

Preparation of 7-fluoro-6-(4-iodo-2-methyl-phenvlamino)-1 H-benzothiazole-5-carboxylic acid cyclopropylmethoxy-amide The compound 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzothiazole-5-carboxylic acid is treated as in Step b, Example 3.

Preparation of 8-fluoro-7-(4-iodo-2-methyl-phenylamino)-auinoxaline-6-carboxvlic acid Step a: Preparation of 8-fli.ioro-7-(2-methyl-phenylamino -guinoxaline-6-carboxylic acid The compound methyl 4, 5-diamino-3-fluoro-2-(2-methyl-phenylamino)-benzoate (from Step e, Example 1) is dissolved in 2:1:1.2 v/v/v of 2.0 M
acetic acid-4.0 M sodium acetate.-methanol. The suspension is warmed to 65 C (or until homogeneous) and the clear solution is poured into a 0.078 M aqueous sodium glyoxal bisulfite (Aldrich, monohydrate, 1.05 equiv.) solution which is warmed to 70 C. The reaction mixture is stirred gently between 55-75 C for one hour, and is then cooled to 12 C with an ice-water bath. Pulverized sodium hydroxide pellets (27 equiv.) are added to the cold solution. The mixture is gently warmed to 30 C and stirred for 45 minutes. The temperature is raised to 70 C
for 15 minutes. The mixture is allowed to cool and is treated with ethyl acetate.
The biphasic mixture is treated with concentrated aqueous hydrochloric acid to achieve pH 0 in the aqueous phase. The organic phase is separated, dried (MgSO4), and concentrated in vacuo to give the desired product. The product may be triturated with an appropriate solvent like dichloromethane or recrystallized from a solvent like ethanol for further purification as necessary.
Step b: Preparation of 8-fluoro-7-(4-iodo-2-methyl phenylamino)-guinoxaline-6-carboxylic acid The compound 8-fiuoro-7-(2-methyl-phenylamino)-quinoxaline-6-carboxylic acid is treated as in Step i, Example 4.

Preparation of 8-fluoro-7-(4-iodo-2-methyl-phenylamino)-auinoxaline-6-carboxylic acid hydroxyamide Step a: Preparation of 8-fluoro-7-(4-iodo-2-methyl-phenylamino)-guinoxaline-6-carboxvlic acid O-(tetrahydro-2H-pyran-2-yl)-oxvamide The compound 8-fluoro-7-(4-iodo-2-methyl-phenylamino)-quinoxaline-6-carboxylic acid is treated as in Step a, Example 2.
Step b: Preparation of 8-fluoro-7-(4-iodo-2-methyl-phenylamino)-guinoxaline-6-carboxvlic acid hydroxyarnide The compound 8-fluoro-7-(4-iodo-2-methyl-phenylamino)-quinoxaline-6-carboxylic acid O-(tetrah)tdro-2H-pyran-2-yl)-oxyamide is treated as in Step b, Example 2.

Preparation of 8-fluoro-7-~4-iodo-2-methvl-phenylamino)-guinoxaline-6-carboxylic acid cyclopropylmethoxv-amide The compound 8=fluoro-7-(4-iodo-2-methyl-phenylamino)-quinoxaline-6-carboxylic acid is treated as in Step b, Example 3.

Preparation of 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-benzof1,2,51thiadiazole-5-carboxylic acid Step a: Preparation of inethyl 7-fluoro-6-(2-methyl-phenylamino)-benzof 1,2,5]thiadiazole-5-carboxylate To a stirring solution comprised of methyl 4,5-diamino-3-fluoro-2-(2-methyl-phenylamino)-benzoate (from Step e, Example 1) and diisopropylethylamine (2 equiv.) in an appropriate solvent like diethyl ether or toluene is added a reagent like N-thioaniline or thionyl chloride (1.35 equiv.). The reaction mixture is brought to reflux for one hour. The rnixture is quenched with dilute aqueous hydrochloric acid. The organic phase is washed with saturated aqueous sodium bicarbonate and brine, is dried (MgSO4), and is concentrated in vacuo to afford the desired product. The product may be recrystallized with an appropriate solvent like chloroform or ethanol, or mery be chromatographed if further purification is necessary.

Alternative method: The cornpound methyl 4,5-diamino-3-fluoro-2-(2-methyl-phenylamino)-benzoate is added to a stirring solution of sulfur monochloride (6 equiv.) in N,N-dimethylformamide and the mixture is gradually heated to 75-80 C. After 5 hours the mixture is cooled to 10 C, water is slowly added. The mixture is extracted with a solvent like diethyl ether or dichloromethane. The organic extract is dried (MgSO4) and is concentrated in vacuo to afford the desired product. The product may be recrystallized with an appropriate solvent like chloroform or ethanol, or may be chromatographed if further purification is necessary.

Step b: Preparation of methyl 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-benzoj1,2, 5lthiadiazole-5-carboxylate The compound methyl 7-fluoro-6-(2-methyl-phenylamino)-benzo[1,2,5]thiadiazole-5-carboxylate is treated as in Step i, Example 4.

Step c: Preparation of 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-benzo[1,2,51thiadiazole-5-carboxylic acid The compound methyl 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-benzo[1,2,5]thiadiazoie-5-carboxylate is treated as in Step j, Example 4.

Preparation of 7-fluoro-6-(4-iodo-2-methyl-phenvlamino)-benzo[1.2, 5]thiadiazole-5-carboxylic acid hydroxvamide Step a: Preparation of 7-fluoiro-6-(4-iodo-2-methyl-phenylamino)-benzo[1.2,51thiadiazole-5-carboxylic acid O-(tetrahydro-2H-pyran-2-yi)-oxyamide The compound 7-fluoiro-6-(4-iodo-2-methyl-phenylamino)-benzo[1,2,5]thiadiazole-5-carboxylic acid is treated as in Step a, Example 2.
Step b: Preparation of 7-fluoro-6-(4-iodo-2-methvl-ahenylamino)-benzo(1,2.5]thiadiazoie-5-carboxvlic acid hydroxyamide The compound 7-fluoiro-6-(4-iodo-2-methyl-phenylamino)-benzo[1,2,5]thiadiazole-5-carboxylic acid O-(tetrahydro-2H-pyran-2-yl)-oxyamide is treated as in Step b, Exarriple 2.

Preparation of 7-fluoro-6-(4-iiodo-2-methvl-ghenylamino)-benzof1.2.51thiadiazole-5-carboxylic acid cyclopropylmethoxy-amide The compound 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-benzo[1,2,5]thiadiazole-5-carboxylic acid is treated as in Step b, Example 3.

Preparation of 7-fluoro-6-(4-iodo-2-methyl-phenyiamino)-benzof 1,2,51oxadiazole-5-carboxyJic acid Step a: Preparation of inethyl 7-fluoro-6-(2-methyl-phenylamino)-benzof 1,2,5]oxadiazole-5-carbox_ylate 2-oxide See Takakis, I. M.; Hadjimihalakis, P. M., J. Heterocyclic Chem., 27, 177 (1990).
A mixture comprised of methyl 4-amino-3-fluoro-2-(2-methyl-phenylamino)-5-nitrobenzoate (from Step d, Example 1) and iodosobenzenediacetate (1.76 equiv.) in benzene is stirred at ambient temperature for 5 hours. The mixture is concentrated in vacuo and the residue purified by column chromatography to give the desired product.

Alternative method: A solution comprised of methyl 4-amino-3-fluoro-2-(2-methyl-phenylamino)-5-nitrobenzoate (0.86 M) in tetrahydrofuran is diazotized and the diazonium salt is treated in situ with sodium azide as described by Smith, P.
A.
S.; Boyer, J. H., Org. Synth., 31, 14 (1951) and references 4 and 8 cited therein.
Thermolysis of this intermediiate in ethylene glycol at 110-120 C for one hour affords the desired product.
Step b: Preparation of inethyl 7-fluoro-6-(2-methyl-ghenylamino)-benzo[1,2,5]oxadiazole-5-carboxylate A solution comprised of methyl 7-fluoro-6-(2-methyl-phenylamino)-benzo[1,2,5]oxadiazole-5-carboxylate 2-oxide and sodium azide (1.38 equiv.) in ethylene glycol is heated to '140-150 C for 30 minutes to obtain, after column chromatography, the desirecl product.

Step c: Preparation of inethyl 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-benzojl,2, 5loxadiazole-5-calrboxylate The compound methyl 7-fluoro-6-(2-methyl-phenylamino)-benzo[1,2,5]oxadiazole-5-cairboxylate is treated as in Step i, Example 4.

Step d: Preparation of 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-benzof 1.2, 5loxadiazole-5-carboxylic acid The compound methyl 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-benzo[1,2,5]oxadiazole-5-carboxylate is treated as in Step j, Example 4.

Preparation of 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-benzof 1,2,51oxadiazole-5-carboxylic acid hvdroxyamide Step a: Preparation of 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-benzof 1,2,51oxadiazole-5-carboxylic acid O-(tetrahydro-2H-pyran-2-yl)-oxyamide The compound 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-benzo[12,5]oxadiazole-5-carboxylic acid is treated as in Step a, Example 2.
Step b: Preparation of 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-benzof 1,2,51oxadiazole-5-carboxvlic acid hydroxyamide The compound 7-fluoiro-6-(4-iodo-2-methyl-phenylamino)-benzo[1,2,5]oxadiazole-5-carboxylic acid O-(tetrahydro-2H-pyran-2-yl)-oxyamide is treated as in Step b, Exarriple 2.

Preparation of 7-fluoro-6-(4-iiodo-2-methvl-phenylamino)-benzo[1,2,5]oxadiazole-5-carboxylic acid cyclopropylmethoxv-amide The compound 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-benzo[1,2,5]oxadiazole-5-ca,rboxylic acid is treated as in Step b, Example 3.

Preparation of 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzotriazole-5-carboxylic acid Step a: Preparation of inethvl 7-fluoro-6-(2-methyl-phenyiamino)-1 H-benzotriazole-5-carboxylate The compound methyl 4,5-diamino-3-fluoro-2-(2-methyl-phenylamino)-benzoate (from Step e, Exannple 1) is diazotized by ordinary methods. Workup gives the desired product.

Step b: Preparation of inethyl 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzotriazole-5-carboxylate The compound methyl 7-fluoro-6-(2-methyl-phenylamino)-1 H-benzotriazole-5-carboxylate is treated as in Step i, Example 4.

Step c: Preparation of 7-fluoro-6-(4-iodo-2-methyl-phenvlamino)-1 H-benzotriazole-5-carboxylic acid The compound methyl 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzotriazole-5-carboxylate is treated as in Step j, Example 4.

Preparation of 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzotriazole-5-carboxylic acid hydroxvamide Step a: Preparation of 7-fluoro-6-(4-iodo-2-methvl-phenylamino)-1 H-benzotriazole-5-carboxylic acid O-(tetrahydro-2H-pyran-2-yl)-oxyamide The compound 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzotriazole-5-carboxylic acid is treated as in Step a, Example 2.
Step b: Preparation of 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzotriazole-5-carboxvlic acid hydroxyamide The compound 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzotriazole-5-carboxylic aicid O-(tetrahydro-2H-pyran-2-yl)-oxyamide is treated as in Step b, Example 2.

Preparation of 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzotriazole-5- .
carboxvlic acid cvclopropylmethoxy-amide The compound 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1 H-benzotriazole-5-carboxylic acid is treated as in Step b, Example 3.

Cascade assay for inhibitors of the MAP kinase pathway Incorporation of 32P into myelin basic protein (MBP) is assayed in the presence of a glutathione S-transferase fusion protein containing p44MAP
kinase (GST-MAPK) and a glutathione S-transferase fusion protein containing p45MEK
(GST-MEK). The assay solijtion contains 20 mM HEPES, pH 7:4; 'I-O mM MgCI2, 1 mM EGTA, 50 M [-y-32P]ATP, 10 g GST-MEK, 0.5 g GST-MAPK and 40 g MBP in a final volume of 100 L. Reactions are stopped after 20 minutes by addition of trichloroacetic acid and filtered through a GF/C filter mat. 32P
retained on the filter mat is determined using a 120S Betaplate. Compounds are assessed at 10 M for ability to inhibit incorporation of 32P.
To ascertain whether compounds are inhibiting GST-MEK or GST MAPK, two additional protocols are employed. In the first protocol, compounds are added to tubes containing GST-MEK, followed by addition of GST-MAPK, MBP
and [y-32P]ATP. In the second protocol, compounds are added to tubes containing both GST-MEK and GST-MAPK, followed by MBP and [Y-32P]ATP.
Compounds that show activity in both protocols are scored as MAPK
inhibitors, while compounds showing activity in only the first protocol are scored as MEK inhibitors.

In vitro MAP kinase assay Inhibitory activity can be confirmed in direct assays. For MAP kinase, 1 g GST-MAPK is incubated with 40 g MBP for 15 minutes at 30 C in a final volume of 50 L containing :i0 mM Tris (pH 7.5), 10 M MgC12, 2 M EGTA, and M [y-32P]ATP. The reaction is stopped by addition of Laemmli SDS sample buffer and phosphorylated NIBP resolved by electrophoresis on a 10%
polyacrylamide gel. Radioactivity incorporated into MBP is determined by both 10 autoradiography, and scintillation counting of excised bands.

In vitro MEK assay For evaluation of direct MEK activity, 10 g GST-MEK, is incubated with 5 g of a glutathione S-transferase fusion protein containing p44MAP kinase with a lysine to alanine mutation iat position 71 (GST-MAPK-KA). This mutation eliminates kinase activity of MAPK, so only kinase activity attributed to the added MEK remains. Incubations are 15 minutes at 30 C in a final volume of 50 L
containing 50 mM Tris (pH 7.5), 10 M MgC12, 2, M EGTA, and 10 M
[y-32P]ATP. The reaction is stopped by addition of Laemrnli SDS sample buffer.
Phosphorylated GST-MAPK-KA is resolved by electrophoresis on a 10%
polyacrylamide gel. Radioactivity incorporated into GST-MAPK-KA is determined by autoradiography, and subsequent scintillation counting of excised bands.
Additionally, an artificially activated MEK containing serine to glutamate mutations at positions 218 and 222 (GST-MEK-2E) is used. When these two sites are phosphorylated, MEK activity is increased. Phosphorylation of these sites can be mimicked by mutation of the serine residues to glutamate. For this assay, 5 g GST-MEK-2E is incubated with 5 g GST-MAPK-KA for 15 minutes at 30 C in the same reactiori buffer as described above. Reactions are terminated and analyzed as above.

Whole cell MAP kinase assav To determine if compounds block activation of MAP kinase in whole cells, the following protocol is used. Cells are plated in multi well plates and grown to confluence. Cells are serum-deprived ovemight. Cells are exposed to the desired concentrations of coriipound or vehicle (DMSO) for 30 minutes, followed by addition of a growth factor, for example, PDGF (100 ng/mL). After a 5-minute treatment with the growth factor, cells are washed with PBS, and lysed in a buffer consisting of 70 mM NaCI, 10 mM HEPES (pH 7.4), 50 mM glycerol phosphate, *
and 1% Triton X-100. Lysates are clarified by centrifugation at 13,000 x g for minutes. Five to fifteen micrograms of protein fromthe resulting supematants are subjected to SDS/PAGE and Westem blotting for phosphorylated MAP kinase levels.

Monolayer growth Cells are plated into multi-well plates at 10 to 20,000 cells/mL. Forty-eight hours after seeding, test compounds are added to the cell growth medium and incubation is continued for 2 additional days. Cells are then removed from the *
wells by incubation with trypsin and enumerated with a Coulter counter.

Growth in soft-aQar Cells are seeded into 35-mm dishes at 5 to 10,000 cells/dish using growth medium containing 0.3% agar. After chilling to solidify the agar, cells are transferred to a 37 C incubator. After 7 to 10 days' growth. visible colonies are manually enumerated with the aid of a dissecting microscope.

*Trade-mark Collagen-Induced Arthritis in Mice Type II collagen-induced arthritis (CIA) in mice is an experimental model of arthritis that has a number of pathologic, immunologic, and genetic features in common with rheumatoid arthritis. The disease is induced by immunization of DBA/1 mice with 100 Ng type 11 collagen, which is a major component of joint cartilage, delivered intradermally in Freund's complete adjuvant. The disease susceptibility is regulated by the class II MHC gene locus, which is analogous to the association of rheumatoid arthritis with HLA-DR4.
A progressive and inflammatory arthritis develops in the majority of mice immunized, characterized by paw width increases of up to 100%. A test compound is administered to mice in a range of amounts, such as 20, 60, 100, and 200 mg/kg body weight/day. The duration of the test can be several weeks to a few months, such as 40, 60, or 80 days. A clinical scoring index is used to assess disease progression from erythema and edema (stage 1), joint distortion (stage 2), to joint ankylosis (stage 3). The disease is variable in that it can affect one or all paws in an animal, resufting in a total possible score of 12 for each mouse. Histopathology of an arthritic joint reveals synovitis, pannus formation, and cartilage and bone erosions. All mouse strains that are susceptible to CIA
are high antibody 'responders to type II collagen, and there is a marked cellular response to CII.

SCW-induced monoarticular arthritis Arthritis is induced as described by Schwab, et al., Infection and Immunity, 59:4436-4442 (1991) with minor modifications. Rats receive 6 g sonicated SCW
[in 10 l Dulbecco's PBS (DPBS)] by an intraarticular injection into the right tibiotalar joint on day 0. On day 21, the DTH is initiated with 100 g of SCW
(250 l) administered i.v. For oral compound studies, compounds are suspended in vehide (0.5% hydroxypropyl-methylcellulose/0.2% Tween 80), sonicated, and administered twice daily (10 ml/kg volume) beginning 1 hr prior to reactivation *Trade-mark with SCW. Compounds are administered in amounts between 10 and 500 mg/kg body weight/day, such as 20, 30, 60, 100, 200, and 300 mg/kg/day. Edema measurements are obtained by determining the baseline volumes of the sensitized hindpaw before reactivation on day 21, and comparing them with volumes at subsequent time points such as day 22, 23, 24, and 25. Paw volume is determined by mercury plethysmography.

Mouse ear-heart transAlant model Fey, T.A. et al. describe methods for transplanting split-heart neonatal cardiac grafts into the ear pinna of mice and rats (J. Pharrn. and Toxic.
Meth.
39:9-17 (1998)). Compounds are dissolved in solutions containing combinations of absolute ethanol, 0.2% hydroxypropyl methylcellulose in water, propylene glycol, cremophor, and dextrose, or other solvent or suspending vehicle. Mice are dosed orally or intraperitoneally once, twice or three times daily from the day of transplant (day 0) through day 13 or until grafts have been rejected. Rats are dosed once, twice, or three times daily from day 0 through day 13. Each animal is anesthetized and an incision is made at the base of the recipient ear, cutting only the dorsal epidermis and dermis. The incision is spread open and down to the cartilage parallel to the head, and sufficiently wide to accommodate the appropriate tunneling for a rat or insertion tool for a mouse. A neonatal mouse or rat pup less than 60 hours old is anesthetized and cervically dislocated. The heart is removed from the chest, rinsed with saline, bisected longitudinally with a scalpel, and rinsed with sterile saline. The donor heart fragment is placed into .25 the preformed tunnel with the insertion tool and air or residual fluid is gently expressed from the tunnel with light pressure. No suturing, adhesive bonding, bandaging, or treatment with antibiotics is required.
Implants are examined at 10-20-fold magnification with a stereoscopic dissecting microscope without anesthesia. Recipients whose grafts are not visibly beating may be anesthetized and evaluated for the presence of electrical *
activity using Grass E-2 platinum subdermal pin microelectodes placed either in the pinna or directly into the graft and a tachograph. Implants can be examined *Trade-mark 62 1-4 times a day for 10, 20, 30 or more days. The ability of a test compound to ameliorate symptoms of transplant rejection can be compared with a control compound such as cyclosporine, tacrolimus, or orally-administered lefluonomide.

Murine ovalbumin-induced eosinophilia Female C57BL/6 mice are obtained from the Jackson Laboratory (Bar Harbor, ME). All animals are given food and water ad libitum. Mice are sensitized *
with a single i.p. injection of OVA (grade V. Sigma Chemical Company, St.
Louis, MO) adsorbed to alum, (10 g OVA + 9 mg alum in 200 l saline) or vehicle control, (9 mg alum in 200 l saline) on day 0. On day 14, the mice are challenged with a 12-minute inhalation of an aerosol consisting of 1.5% OVA
(weight/volume) in saline produced by a nebulizer (small particle generator, *
model SPAG-2; ICN Pharmaceuticals, Costa Mesa, CA). Groups of eight mice are dosed with oral vehicle (0.5% hydroxypropylmethylcellulose / 0.25% TWEEN-80), or a test compound at 10, 30, or 100 mg/kg in oral vehicle, 200 l per mouse p.o. Dosing is performed once per day starting on day 7 or day 13, and extending through day 16.
For determination of pulmonary eosinophilia, three days after the first OVA aerosol challenge (day 17), the mice are anesthetized with an i.p.
injection of anesthetic (Ketamine/Acepromazine/Xylazine), and the tracheae is exposed and cannulated. The lungs and upper airways are lavaged twice with 0.5 ml of cold PBS. A portion (200 NI) of the bronchoalveolar lavage (BAL) fluid is enumerated using a Coulter counter Model ZB1 (Coulter Electronics, Hialeah, FL). The remaining BAL fluid is then centrifuged at 300 x g for flve minutes, and the cells are resuspended in 1 ml of HBSS (Gibco BRL) containing 0:5% fetal calf serum (HyClone) and 10 mM HEPES (Gibco BRL). The cell suspension is centrifuged in a cytospin (Shandon Southern Instruments, Sewickley, PA) and *
stained by Diff Quick (American Scient'rf'ic Products, McGraw Park, IL) to differentiate BAL leukocytes into neutrophil, eosinophil, monocyte or lymphocyte *Trade-mark subsets. The number of eosinophits in the BAL fluid is determined by multiplying the percentage of eosinophils by the total cell count.

Caco-2 cell studies Cell transport studies were conducted with Caco-2 cells grown on *
Snapwells between 22 to 28 days postseeding. Typically, 10 mM MES buffer (pH
6.5) with 5 mM KCI, 135 mM NaCI and 1.8 mM CaCl2 was used for the apical side and 10 mM MOPS (pH 7.4) with 5 mM KCI, 132.5 mM NaCl and 1.8 mM
CaCl2 with 5 mM D-Glucose was used for the basolateral side. After washing the monolayers, appropriate buffers were pipetted into the respective chambers and the cells were pre-equilibrated at 37 C for at least 15 min. On the day of the experiment the growth media was aspirated and the cell monolayers were preequilibrated with appropriate buffers at 37 C for at least 15 min.
Thereafter, TEER measurements were performed to confirm the integrity of the monolayers.
Transepithelial flux measurements were made by mounting the cell monolayers in a side-by-side diffusion chamber system (Precision Instrument Design, Tahoe City, CA). Temperature was maintained at 37 C with a circulating water jacket.
The solutions were mixed with gas-lift circulation with 95% oxygen-5% carbon dioxide. Donor solutions with PD compounds, [14C] mannitol (leakage marker) and [3Hj metoprolol (reference compound) were added to the apical chamber.
Donor and receiver samples were collected at selected time intervals for up to hours. Radiolabelled mannitol and metoprolol were analyzed using scintillation *
counting (TopCount, Packard Instruments, Downers Grove, IL). PD compounds were analyzed using a LC/MS/MS method. Apparent permeability coefficients were calculated using the following equation:

PaPP = (V' dC) / (A.Co. dt) where V= volume of the receiver solution in ml, A = surface area in cm2, C _ initial donor concentration in mM and dC/dt = change in the drug concentration in the receiver chamber over time.
*Trade-mark Metabolic Stability in Human and Rat Liver Microsomes Compounds are individually incubated (5 pM, dissolved in DMSO) with human and rat liver microsomes (0.5 mg/mL protein) in 50 mM KHPO4 buffer at 37 C in the presence of 1.0 mM NADPH. At 0, 10, 20 and 40 minutes, 100 NL
aliquots. are removed and added to 300 pL of acetonitrile. Standard curves are run in a similar manner with each compound at concentrations: 7.5 pM, 3.75 PM, 2.5 pM, 1.25 pM. The samples are analyzed for parent concentration by LC/MS/MS. The in vitro metabolic half-life determinations are determined from *
the concentration vs. time plots using WinNonlin. These in vitro data represent the rate of oxidative and hydrolytic metabolism.

F. OTHER EMBODIMENTS
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.

What is claimed is:

*Trade-mark

Claims

1. A compound of the following formula (I):

wherein W is OR1, NR2OR1, NR A R B, NR2NR A R B, O(CH2)2-4NR A R B, or NR2(CH2)2-4 NR
A R B;
R1 is H, C 1-8 alkyl, C 3-8 alkenyl, C 3-8 alkynyl, C 3-8 cycloalkyl, phenyl, (phenyl)-C 1-4 alkyl, (phenyl)C 3-4 alkenyl, (phenyl)C 3-4 alkynyl, (C 3-8 cycloalkyl)C
1-4 alkyl, (C 3-8 cycloalkyl)C 3-4 alkenyl, (C 3-8 cycloalkyl)C 3-4 alkynyl, C3-8 heterocyclic radical, (C 3-8 heterocyclic radical)C 1-4 alkyl, (C 3-8 heterocyclic radical)-C 3-4 alkenyl, (C 3-8 heterocyclic radical)C 3-4 alkynyl or (CH2)2-4 NR c R D
;
R2 is H, C 1-4 alkyl, phenyl, C 3-6 cycloalkyl, C 3-6 heterocyclic radical, or (C 3-6 cycloalkyl) methyl;

R A is H, C 1-6 alkyl, C 3-8 alkenyl, C 3-8 alkynyl, C 3-8 cycloalkyl, phenyl, (C 3-8 cycloalkyl)C 1-4 alkyl, (C 3-8 cycloalkyl)C 3-4 alkenyl, (C 3-8 cycloalkyl)C 3-4 alkynyl, C 3-8 heterocyclic radical, (C 3-8 heterocyclic radical)C 1-4 alkyl, (aminosulfonyl)phenyl, [(aminosulfonyl)phenyl]C 1-4 alkyl, (aminosulfonyl)C 1-alkyl, (aminosulfonyl)C 3-6 cycloalkyl, [(aminosulfonyl)C 3-6 cycloalkyl]C 1-4 alkyl, or (CH2)2-4 NR c R D;

R B is H, C1-8 alkyl, C3-8 alkenyl, C 3-8 alkynyl, C 3-8 cycloalkyl, or phenyl;

Q is one of the following formulae (i) - (iii):
R3 is H or F;

R4 is halo, NO2, SO2NR o(CH2)2-4NR E R F, SO2NR E R F, or (CO)T;

T is C 1-8 alkyl, C 3-8 cycloalkyl, (NR E R F)C 1-4 alkyl, OR F, -NR o(CH2)2-4 NR E R F, or NR E R F;

Z is one of the following formulae (iv) - (viii):
one of R5 and R6 is H or methyl and the other of R5 and R6 is H, C1-6 alkyl, alkenyl, C2-6 alkynyl, phenyl, benzyl, or -M-E-G;

M is O, CO, SO2, NR j, (CO)NR H, NR H (CO), NR H (SO2), (SO2)NR H, or CH2;
E is (CH2)1-4 or (CH2)m, O(CH2)p where 1 <= (each of m and p) <= 3 and 2<=(m + p)<= 4; or E is absent;
G is R K, OR i or NR J R K, provided that if p = 1, then G is H;

R7 is H, C 1-4 alkyl, C 2-4 alkenyl, C 2-4 alkynyl, C3-6 cycloalkyl, phenyl, 2-pyridyl, 3-pyridyl, 4-pyridyl, (CH2)1-2Ar, where Ar is phenyl, 2-pyridyl, 3-pyridyl, or 4-pyridyl, SO2NR H(CH2)2-4 NR J R K, (CO)(CH2)2-4NR J R K or (CO)NR H(CH2)2-4NR J R K;

X1 is O, S, NR8, or CHR9; X2 is O, S, or CHR9; and X3 is O or S; where if X, or X2 is CHR9, said compound may also be a tautomerized indole;

R8 is H, C 1-4 alkyl, phenyl, 2-pyridyl, 3-pyridyl, 4-pyridyl, (CH2)1-2Ar, where Ar is phenyl, 2-pyridyl, 3-pyridyl, or 4-pyridyl, C 2-4 alkenyl, C 2-4 alkynyl, C 3-cycloalkyl, or (C 2-4 alkyl)NR L R M; provided R7 and R8 together have no more than 14 carbon atoms, exclusive of R L, R M, R J and R K;

R G is C 1-4 alkyl, phenyl, 2-pyridyl, 3-pyridyl, 4-pyridyl, C3-4 alkenyl, C 3-4 alkynyl, C 3-6 cycloalkyl, (CO)OR p, (C 2-4 alkyl)NR L R M, (CO)NR N(CH2)2-4NR L R M, (CO)NR L R M, (CO)(CH2)2-4 -NR L R M, or (CH2)1-2Ar, where Ar is phenyl, 2-pyridyl, 3-pyridyl, or 4-pyridyl;

R g is C1-4 alkyl, phenyl, 2-pyridyl, 3-pyridyl, 4-pyridyl, C 2-4 alkenyl, C 2-4 alkynyl, C 3-6 cycloalkyl, (CO)OR P,(C 2-4 alkyl)NR L R M, (CO)NR N(CH2)2-4NR L R M, (CO)NR L R M, (CO)(CH2)24 -NR L R M, or (CH2)1-2Ar', where Ar' is phenyl, 2-pyridyl, 3-pyridyl, or 4-pyridyl;

R P is H, C 1-6 alkyl, phenyl, C 3-4 alkenyl, C 3-4 alkynyl, C 3-6 cycloalkyl, or (CH2)2-4 NR L R M;

R10 is H, methyl, halo, or NO2;
R11 is H, methyl, halo, or NO2;

each of R C, R D, R E, R F, R I R J, R K, R L and R M is independently selected from H, C 1-4 alkyl, C 3-4 alkenyl, C 3-4, alkynyl, C 3-6 cycloalkyl, and phenyl; each of NR C R D,NR E R F, NR J R K, and NR L R M can also independently be morpholinyl, piperazinyl, pyrrolidinyl, or piperadinyl; and each of R H, R N, and R O is independently H, methyl, or ethyl;

wherein each hydrocarbon radical or heterocyclic radical above is optionally substituted with between 1 and 3 substituents independently selected from halo, C 1-4 alkyl, C 3-6 cycloalkyl, C 3-4 alkenyl, C 3-4 alkynyl, phenyl, hydroxyl, amino, (amino)sulfonyl, and NO2, wherein each substituent alkyl, cycloalkyl, alkenyl, alkynyl or phenyl is in turn optionally substituted with between 1 and 3 substituents independently selected from halo, C 1-2 alkyl, hydroxyl, amino, and NO2;

or a pharmaceutically acceptable salt or C 1-7 ester thereof.

2. A compound of claim 1, wherein Q is formula (i).

3. A compound of claim 2, wherein R3 is H or fluoro.

4. A compound of claim 3, wherein R4 is fluoro, chloro, or bromo.

5. A compound of'claim 1, wherein Rio is hydrogen, methyl, fluoro, or chloro.

6. A compound of' claim 1, wherein R11 is methyl, chloro, fluoro, nitro, or hydrogen.

7. A compound of claim 6, wherein R11 is H.

8. A compound of claim 6, wherein R11 is fluoro.

9. A compound of claim 5, wherein each of R10 and R11 is fluoro.

10. A compound of claim 1, wherein R1 is H, methyl, ethyl, propyl, isopropyl, isobutyl, benzyl, phenethyl, allyl, C 3-5 alkenyl, C 3-6 cycloalkyl, (C 3-5 cycloalkyl)C 1-2 alkyl, (C 3-5 heterocyclic radical)C 1-2 alkyl, or (CH2)2-4 NR C R D.

11. A compound of claim 10, wherein R1 is H or (C 3-4 cycloalkyl)C 1-2 alkyl.

12. A compound of claim 1, wherein R2 is H or methyl.

13. A compound of claim 1, wherein R A has at least one hydroxyl substituent.

14. A compound of claim 1, wherein R A is H, methyl, ethyl, isobutyl, hydroxyethyl, phenyl, 2-piperidin-1-yl-ethyl, 2,3-dihydroxy-propyl, 3-[4-(2-hydroxyethyl)-piperazin-1-yl]-propyl, 2-pyrrolidin-1-yl-ethyl, or 2-diethylamino-ethyl; and R B is H; or where R B is methyl and R A is phenyl.

15. A compound of claim 1, wherein W is NR A R B or NR2NR A R B.

16. A compound of claim 1, wherein W is NR2(CH2)2-4 NR A R B or O(CH2)2-3 NR A R B.

17. A compound of claim 1, wherein W is NR2OR1.

18. A compound of claim 1, wherein W is OR1.

19. A compound of claim 1, wherein Z is formula (v).

20. A compound of claim 19, wherein X1 is NR8, and R7 is H.

21. A compound of claim 1 having the structure 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1H-benzoimidazole-5-carboxylic acid.

22. A compound of claim 1 selected from 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1H-benzoimidazole-5-carboxylic acid; 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-benzooxazole-5-carboxylic acid; 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-benzothiazole-5-carboxylic acid; 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-benzo[1,2,5]thiadiazole-5-carboxylic acid; 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-benzo[1,2,5]oxadiazole-5-carboxylic acid; 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-2-(2-hydroxyethyl)-1H-benzoimidazole-5-carboxylic acid; 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-2-(2-dimethylamino-ethyl)-1H-benzoimidazole-5-carboxylic acid; 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1-acetyl-benzoimidazole-5-carboxylic acid; 8-fluoro-7-(4-iodo-2-methyl-phenylamino)-quinoxaline-6-carboxylic acid; and 7-fluoro-6-(4-iodo-2-methyl-phenylamino)-1H-benzotriazole-5-carboxylic acid; and the corresponding hydroxamic acids and cyclopropylmethyl hydroxamates.

23. A pharmaceutical composition comprising a compound of claim 1 and a pharmaceutically-acceptable carrier.

24. Use of pharmaceutically-effective amount of a composition comprising a compound of any one of claims 1 to 22 and a pharmaceutically acceptable carrier to treat a proliferative disease.

25. The use of claim 24, wherein said proliferative disease is selected from psoriasis, restenosis, autoimmune disease, and atherosclerosis.

26. Use of pharmaceutically-effective amount of a composition comprising a compound of any one of claims 1 to 22 and a pharmaceutically acceptable carrier to treat cancer.

27. The use of claim 26, wherein said cancer is MEK-related.

28. The use of claim 26, wherein said cancer is colorectal, cervical, breast, ovarian, brain, acute leukemia, gastric, non-small cell lung, pancreatic or renal cancer.

29. Use of pharmaceutically-effective amount of a composition comprising a compound of any one of claims 1 to 22 and a pharmaceutically acceptable carrier to treat or ameliorate the sequelae of a stroke.

30. Use of pharmaceutically-effective amount of a composition comprising a compound of any one of claims 1 to 22 and a pharmaceutically acceptable carrier to treat or ameliorate the sequelae of heart failure.

31. Use of pharmaceutically-effective amount of a composition comprising a compound of any one of claims 1 to 22 and a pharmaceutically acceptable carrier to treat or reduce the symptoms of xenograft rejection in a patient who has undergone an organ transplant, a limb transplant, cell transplant, a skin transplant, or a bone marrow transplant.

32. Use of pharmaceutically-effective amount of a composition comprising a compound of any one of claims 1 to 22 and a pharmaceutically acceptable carrier to treat osteoarthritis.

33. Use of pharmaceutically-effective amount of a composition comprising a compound of any one of claims 1 to 22 and a pharmaceutically acceptable carrier to treat rheumatoid arthritis.

34. Use of pharmaceutically-effective amount of a composition comprising a compound of any one of claims 1 to 22 and a pharmaceutically acceptable carrier to treat a viral infection.

35. Use of pharmaceutically-effective amount of a composition comprising a compound of any one of claims 1 to 22 and a pharmaceutically acceptable carrier to treat cystic fibrosis.

36. Use of pharmaceutically-effective amount of a composition comprising a compound of any one of claims 1 to 22 and a pharmaceutically acceptable carrier to treat hepatomegaly.

37. Use of pharmaceutically-effective amount of a composition comprising a compound of any one of claims 1 to 22 and a pharmaceutically acceptable carrier to treat cardiomegaly.

38. Use of pharmaceutically-effective amount of a composition comprising a compound of any one of claims 1 to 22 and a pharmaceutically acceptable carrier to treat Alzheimer's disease.

39. Use of pharmaceutically-effective amount of a composition comprising a compound of any one of claims 1 to 22 and a pharmaceutically acceptable carrier to treat a complication of diabetes.

40. Use of pharmaceutically-effective amount of a composition comprising a compound of any one of claims 1 to 22 and a pharmaceutically acceptable carrier to treat septic shock.

41. Use of pharmaceutically-effective amount of a composition comprising a compound of any one of claims 1 to 22 and a pharmaceutically acceptable carrier to treat asthma.

42. Use of pharmaceutically-effective amount of a composition comprising a compound of any one of claims 1 to 22 and a pharmaceutically acceptable carrier in conjunction with radiation therapy or chemotherapy to treat cancer.

43. The use of claim 42, wherein said chemotherapy comprises a mitotic inhibitor.

44. The use of claim 43, wherein said chemotherapy comprises a mitotic inhibitor selected from paclitaxel, docetaxel, vincristine, vinblastine, vinorelbine, and vinflunine.

45. A commercial package comprising a container containing a composition comprising the compound of any one of claims 1 to 22 and a pharmaceutically acceptable carrier and written matter which states that the composition is for use in the treatment of a medical condition selected from:
a) a proliferative disease;
b) cancer;
c) osteoarthritis;
d) rheumatoid arthritis;

e) a viral infection;
f) cystic fibrosis;
g) hepatomegaly;
h) cardiomegaly;
i) Alzheimer's disease;
j) a complication of diabetes;
k) septic shock; and I) asthma.

46. A commercial package comprising a container containing the compound of any one of claims 1 to 22 and written matter which states that the compound is for use in the treatment of a medical condition selected from:
a) a proliferative disease;
b) cancer;
c) osteoarthritis;
d) rheumatoid arthritis;
e) a viral infection;
f) cystic fibrosis;
g) hepatomegaly;
h) cardiomegaly;
i) Alzheimer's disease;
j) a complication of diabetes;
k) septic shock; and l) asthma.

47. A commercial package comprising a container containing a composition comprising the compound of any one of claims 1 to 22 and a pharmaceutically acceptable carrier and written matter which states that the composition is for use in the treatment or amelioration of the symptoms of a medical condition selected from:
a) sequelae of a stroke;
b) sequelae of heart failure; and c) xenograft rejection.

48. A commercial package comprising a container containing the compound of any one of claims 1 to 22 and written matter which states that the compound is for use in the treatment of a medical condition selected from:
a) sequelae of a stroke;
b) sequelae of heart failure; and c) xenograft rejection.