AU2012205127B2 - Diaminotriazole Compounds Useful as Protein Kinase Inhibitors - Google Patents

Abstract

The present invention relates to inhibitors of protein kinases, particularly to inhibitors of JAK2 and JAK3. The invention also provides pharmaceutical compositions comprising the compounds of the invention, processes for preparing the compounds and methods of using the compositions in the treatment of various disorders.

Description

DIAMINOTRIAZOLE COMPOUNDS USEFUL AS PROTEIN KINASE INHIBITORS TECHNICAL FIELD OF THE INVENTION 100011 This application is a divisional of Australian Patent Application No. 2005286968 filed 19 September 2005, the entire contents of which is herein incorporated by cross-reference. The subject matter of this application is related to the applicant's International Patent Application No. PCT/US2005/033333, filed on 19 September 2005, as well as United States Provisional Patent Application No. 60/610,902 filed on 17 September 2004, each of which is herein incorporated by cross-reference. The present invention relates to compounds useful as inhibitors of Janus kinases (JAK). The present invention also relates to compounds useful as inhibitors of Aurora-2 kinase, Flt3 kinase, GSK-3 kinase and KDR. The invention also provides pharmaceutically acceptable compositions comprising the compounds of the invention and methods of using the compositions in the treatment of various disorders. BACKGROUND OF THE INVENTION [00021 The Janus kinases (JAK) are a family of tyrosine kinases consisting of JAKI, JAK2, JAK3 and TYK2. The JAKs play a critical role in cytokine signaling. The down-stream substrates of the JAK family of kinases include the signal transducer and activator of transcription (STAT) proteins. JAK/STAT signaling has been implicated in the mediation of many abnormal immune responses such as allergies, asthma, autoimmune diseases such as transplant rejection, rheumatoid arthritis, amyotrophic lateral sclerosis and multiple sclerosis as well as in solid and hematologic malignancies such as leukemias and lymphomas. JAK2 has also been implicated in myeloproliferative disorders, which include polycythemia vera, essential thrombocythemia, chronic idiopathic myelofibrosis, myeloid metaplasia with myelofibrosis, chronic myeloid leukemia, chronic myelomonocytic leukemia, chronic eosinophilic leukemia, hypereosinophilic syndrome and systematic mast cell disease. 100031 W02004/046120 describes diaminotriazoles useful as inhibitors of protein kinases, including Flt3, FMS, c-Kit, PDGFR, JAK, AGC sub-family of protein kinases, CDK, GSK, Src, ROCK and/or Syk. However, there is a need to develop compounds that are more selective inhibitors of protein kinases, such as those that inhibit Aurora-2, Flt3, KDR, JAK2 and JAK3. In particular, it would be desirable to develop compounds that are useful as inhibitors of JAK family kinases.

SUMMARY OF THE INVENTION [00041 It has now been found that compounds of this invention, and pharmaceutically acceptable compositions thereof, are effective as inhibitors of protein kinases. In certain embodiments, these compounds, and pharmaceutically acceptable compositions thereof, are effective as inhibitors of GSK-3, JAK-2, JAK-3, Flt3, KDR or Aurora-2 protein kinases. In preferred embodiments, these compounds and pharmaceutically acceptable compositions are inhibitors of JAK-2 or JAK-3. These compounds have the general formula I: (ZR )m

H

2 N A N N R N HN (QRX2 ) RX (I) or a pharmaceutically acceptable derivative thereof, wherein the variables are as defined herein. [00051 These compounds and pharmaceutical compositions thereof are useful for treating or preventing a variety of disorders, including, but not limited to, allergies, asthma, autoimmune diseases such as transplant rejection, rheumatoid arthritis, amyotrophic lateral sclerosis and multiple sclerosis, as well as in solid and hematologic malignancies such as leukemias and lymphomas. The compounds and pharmaceuticals compositions thereof are also useful in treating or preventing myeloproliferative disorders, including polycythemia vera, essential thrombocythemia, chronic idiopathic myelofibrosis, myeloid metaplasia with myelofibrosis, chronic myeloid leukemia, chronic myelomonocytic leukemia, chronic eosinophilic leukemia, hypereosinophilic syndrome and systematic mast cell disease. DETAILED DESCRIPTION OF THE INVENTION [00061 Definitions and General Terminology [00071 As used herein, the following definitions shall apply unless otherwise indicated. For purposes of this invention, the chemical elements are identified in accordance with the Periodic Table of the Elements, CAS version, Handbook of Chemistry and Physics, 7 5 th Ed. Additionally, general principles of organic chemistry are described in "Organic Chemistry", Thomas Sorrell, University Science Books, Sausalito: 1999; "March's Advanced Organic 2 Chemistry", 5 'h Ed., Ed.: Smith, M.B. and March, J., John Wiley & Sons, New York: 2001; "Encyclopedia of Organic Transformations"; Ed.: Richard C. Larock, John Wiley & Sons, New York: 1999; "Encyclopedia of Reagents for Organic Synthesis" Ed.: Leo A. Paquette, John Wiley & Sons, New York: 1995; T.W. Greene & P.G.M Wutz, "Protective Groups in Organic Synthesis", 3 'd Edition, John Wiley & Sons, Inc. (1999)(and earlier editions) the entire contents of which are hereby incorporated by reference. [00081 As described herein, compounds of the invention may optionally be substituted with one or more substituents, such as are illustrated generally above, or as exemplified by particular classes, subclasses, and species of the invention. It will be appreciated that the phrase "optionally substituted" is used interchangeably with the phrase "substituted or unsubstituted." In general, the term "substituted", whether preceded by the term "optionally" or not, refers to the replacement of hydrogen radicals in a given structure with the radical of a specified substituent. Unless otherwise indicated, an optionally substituted group may have a substituent at each substitutable position of the group, and when more than one position in any given structure may be substituted with more than one substituent selected from a specified group, the substituent may be either the same or different at every position. Combinations of substituents envisioned by this invention are preferably those that result in the formation of stable or chemically feasible compounds. The term "stable", as used herein, refers to compounds that are not substantially altered when subjected to conditions to allow for their production, detection, and preferably their recovery, purification, and use for one or more of the purposes disclosed herein. In some embodiments, a stable compound or chemically feasible compound is one that is not substantially altered when kept at a temperature of 40*C or less, in the absence of moisture or other chemically reactive conditions, for at least a week. 100091 The term "aliphatic" or "aliphatic group", as used herein, means a straight-chain (i.e., unbranched) or branched, substituted or unsubstituted hydrocarbon chain that is completely saturated or that contains one or more units of unsaturation, or a monocyclic hydrocarbon or bicyclic hydrocarbon that is completely saturated or that contains one or more units of unsaturation, but which is not aromatic (also referred to herein as "carbocycle", "cycloaliphatic", or "cycloalkyl"), that has a single point of attachment to the rest of the molecule. Unless otherwise specified, aliphatic groups contain 1-20 aliphatic carbon atoms. In some embodiments, aliphatic groups contain 1-10 aliphatic carbon atoms. In other embodiments, aliphatic groups contain 1-8 aliphatic carbon atoms. In still other embodiments, aliphatic groups contain 1-6 aliphatic carbon atoms, and in yet other embodiments aliphatic 3 groups contain 1-4 aliphatic carbon atoms. In some embodiments, "cycloaliphatic" (or "carbocycle", or "cycloalkyl") refers to a monocyclic C 3

.

8 hydrocarbon or bicyclic C 8

-

1 2 hydrocarbon that is completely saturated or that contains one or more units of unsaturation, but which is not aromatic, that has a single point of attachment to the rest of the molecule wherein any individual ring in said bicyclic ring system has 3-7 members. Suitable aliphatic groups include, but are not limited to, linear or branched, substituted or unsubstituted alkyl, alkenyl, alkynyl groups and hybrids thereof such as (cycloalkyl)alkyl, (cycloalkenyl)alkyl, or (cycloalkyl)alkenyl. [00101 The term "heteroaliphatic", as used herein, means aliphatic groups wherein one or two carbon atoms are independently replaced by one or more of oxygen, sulfur, nitrogen, phosphorus, or silicon. Heteroaliphatic groups may be substituted or unsubstituted, branched or unbranched, cyclic or acyclic, and include "heterocycle", "heterocyclyl", "heterocycloaliphatic", or "heterocyclic" groups. [00111 The term "heterocycle", "heterocyclyl", "heterocycloaliphatic", or "heterocyclic" as used herein means non-aromatic, monocyclic, bicyclic, or tricyclic ring systems in which one or more ring members are an independently selected heteroatom. In some embodiments, the "heterocycle", "heterocyclyl", "heterocycloaliphatic", or "heterocyclic" group has three to fourteen ring members in which one or more ring members is a heteroatom independently selected from oxygen, sulfur, nitrogen, or phosphorus, and each ring in the system contains 3 to 7 ring members. 100121 Examples of heterocyclic rings include benzimidazolone (e.g., 3-1 H-benzimidazol 2-one, 3-(1 -alkyl)-benzimidazol-2-one), tetrahydrofuranyl (e.g., 2-tetrahydrofuranyl, 3 tetrahydrofuranyl), tetrahydrothiophenyl (e.g., 2-tetrahydrothiophenyl, 3-tetrahydrothiophenyl), morpholino (e.g., 2-morpholino, 3-morpholino, 4-morpholino), thiomorpholino (e.g., 2 thiomorpholino, 3-thiomorpholino, 4-thiomorpholino), pyrrolidinyl (e.g., 1-pyrrolidinyl, 2 pyrrolidinyl, 3-pyrrolidinyl), tetrahydropiperazinyl (e.g., 1-tetrahydropiperazinyl, 2 tetrahydropiperazinyl, 3-tetrahydropiperazinyl), piperidinyl (e.g., I -piperidinyl, 2-piperidinyl, 3-piperidinyl, 4-piperidinyl), pyrazolinyl (e.g., I -pyrazolinyl, 3-pyrazolinyl, 4-pyrazolinyl, 5 pyrazolinyl), thiazolidinyl (e.g., 2-thiazolidinyl, 3-thiazolidinyl, 4-thiazolidinyl), imidazolidiny (e.g., I -imidazolidinyl, 2-imidazolidinyl, 4-imidazolidinyl, 5-imidazolidinyl), indolinyl, tetrahydroquinolinyl, tetrahydroisoquinolinyl, benzothiolane, benzodithiane, and dihydro imidazol-2-one (1,3-dihydro-imidazol-2-one). [00131 The term "heteroatom" means one or more of oxygen, sulfur, nitrogen, phosphorus, or silicon (including, any oxidized form of nitrogen, sulfur, phosphorus, or silicon; the 4 quaternized form of any basic nitrogen or; a substitutable nitrogen of a heterocyclic ring, for example N (as in 3,4-dihydro-2H-pyrrolyl), NH (as in pyrrolidinyl), or NR* (as in N-substituted pyrrolidinyl)). 100141 The term "unsaturated", as used herein, means that a moiety has one or more units of unsaturation. 10015] The term "alkoxy" or "thioalkyl", as used herein, refers to an alkyl group, as previously defined, attached to the principal carbon chain through an oxygen ("alkoxy") or sulfur ("thioalkyl") atom. 100161 The terms "haloalkyl", "haloalkenyl", and "haloalkoxy" means alkyl, alkenyl or alkoxy, as the case may be, substituted with one or more halogen atoms. The term "halogen" means F, Cl, Br, or I. 100171 The term "aryl" used alone or as part of a larger moiety as in "aralkyl", "aralkoxy", or "aryloxyalkyl", refers to monocyclic, bicyclic, and tricyclic ring systems having a total of five to fourteen ring members, wherein at least one ring in the system is aromatic and wherein each ring in the system contains 3 to 7 ring members. The term "aryl" may be used interchangeably with the term "aryl ring". The term "aryl" also refers to heteroaryl ring systems as defined hereinbelow. 100181 The term "heteroaryl", used alone or as part of a larger moiety as in "heteroaralkyl" or "heteroarylalkoxy", refers to monocyclic, bicyclic, and tricyclic ring systems having a total of five to fourteen ring members, wherein at least one ring in the system is aromatic, at least one ring in the system contains one or more heteroatoms, and wherein each ring in the system contains 3 to 7 ring members. The term "heteroaryl" may be used interchangeably with the term "heteroaryl ring" or the term "heteroaromatic". 100191 Examples of heteroaryl rings include furanyl (e.g., 2-furanyl, 3-furanyl), imidazolyl (e.g., N-imidazolyl, 2-imidazolyl, 4-imidazolyl, 5-imidazolyl) benzimidazolyl, isoxazolyl (e.g., 3-isoxazolyl, 4-isoxazolyl, 5-isoxazolyl) oxazolyl (e.g., 2-oxazolyl, 4-oxazolyl, 5-oxazolyl), pyrrolyl, (e.g., N-pyrrolyl, 2-pyrrolyl, 3-pyrrolyl), pyridyl (e.g., 2-pyridyl, 3-pyridyl, 4-pyridyl), pyrimidinyl (e.g., 2-pyrimidinyl, 4-pyrimidinyl, 5-pyrimidinyl), pyridazinyl (e.g., 3 pyridazinyl), thiazolyl (e.g., 2-thiazolyl, 4-thiazolyl, 5-thiazolyl), tetrazolyl (e.g., 5-tetrazolyl), triazolyl (e.g., 2-triazolyl and 5-triazolyl), thienyl, (e.g., 2-thienyl, 3-thienyl), benzofuryl, thiophenyl, benzothiophenyl, indolyl (e.g., 2-indolyl), pyrazolyl (e.g., 2-pyrazolyl), isothiazolyl, oxadiazolyl (e.g., 1,2,3-oxadiazolyl), oxadiazolyl (e.g., 1,2,5-oxadiazolyl), oxadiazolyl (e.g., 1,2,4-oxadiazolyl), triazolyl (e.g., 1,2,3-triazolyl), thiadiazolyl (e.g., 1,2,3-thiadiazolyl), thiadiazolyl (e.g., 1,3,4-thiadiazolyl), thiadiazolyl (e.g., 1,2,5-thiadiazolyl), purinyl, pyrazinyl, 5 triazinyl (e.g., 1,3,5-triazinyl), quinolinyl (e.g., 2-quinolinyl, 3-quinolinyl, 4-quinolinyl), and isoquinolinyl (e.g., 1 -isoquinolinyl, 3-isoquinolinyl, or 4-isoquinolinyl). [00201 An aryl (including aralkyl, aralkoxy, aryloxyalkyl and the like) or heteroaryl (including heteroaralkyl and heteroarylalkoxy and the like) group may contain one or more substituents. Suitable substituents on the unsaturated carbon atom of an aryl or heteroaryl group are selected from halogen; -R*; -OR*; -SR*; 1,2-methylenedioxy; 1,2-ethylenedioxy; phenyl (Ph) optionally substituted with R 0 ; -O(Ph) optionally substituted with R 0 ; -(CH 2

)

1

-

2 (Ph) optionally substituted with R 0 ; -CH=CH(Ph) optionally substituted with R 0 ; -NO 2 ; -CN;

-N(R*)

2 ; -NR 0 C(O)R*; -NR*C(S)R 0 ; -NR*C(O)N(R*) 2 ; -NR*C(S)N(R) 2 ; -NR'CO 2 R*;

-NR*NR

0

C(O)R

0 ; -NR*NR 0

C(O)N(R*)

2 ; -NR*NR*CO 2 R'; -C(O)C(O)R*; -C(O)CH 2 C(O)R*; -C0 2

R

0 ; -C(O)R 0 ; -C(S)R*; -C(O)N(R*) 2 ; -C(S)N(R*) 2 ; -C(=NH)-N(R*) 2 , -OC(O)N(R) 2 ; -OC(O)R*; -C(O)N(OR*) R*; -C(NOR*) R*; -S(O) 2 R*; -S(0) 3 R*; -SO 2

N(R')

2 ; -S(O)R*;

-NR*SO

2

N(R*)

2 ; -NR*SO 2 R*; -N(OR*)R*; -C(=NH)-N(R) 2 ; or -(CH 2 )o- 2 NHC(O)R* wherein each independent occurrence of R 0 is selected from hydrogen, optionally substituted CI-6 aliphatic, an unsubstituted 5-6 membered heteroaryl or heterocyclic ring, phenyl, -O(Ph), or

-CH

2 (Ph), or, notwithstanding the definition above, two independent occurrences of R*, on the same substituent or different substituents, taken together with the atom(s) to which each R* group is bound, form a 5-8-membered heterocyclyl, aryl, or heteroaryl ring or a 3-8-membered cycloalkyl ring having 0-3 heteroatoms independently selected from nitrogen, oxygen, or sulfur. Optional substituents on the aliphatic group of R* are selected from NH 2 , NH(CI4 aliphatic),

N(C

14 aliphatic) 2 , halogen, C 1

.

4 aliphatic, OH, O(CI 4 aliphatic), NO 2 , CN, CO 2 H, CO 2

(C

14 aliphatic), O(halo CIA aliphatic), or halo(C 14 aliphatic), wherein each of the foregoing Cia aliphatic groups of R* is unsubstituted. 100211 An aliphatic or heteroaliphatic group, or a non-aromatic heterocyclic ring may contain one or more substituents. Suitable substituents on the saturated carbon of an aliphatic or heteroaliphatic group, or of a non-aromatic heterocyclic ring are selected from those listed above for the unsaturated carbon of an aryl or heteroaryl group and additionally include the following: =0, =S, =NNHR*, =NN(R*) 2 , =NNHC(O)R*, =NNHCO 2 (alkyl), =NNHSO 2 (alkyl), or =NR*, where each R* is independently selected from hydrogen or an optionally substituted

C

1

.

6 aliphatic. Optional substituents on the aliphatic group of R* are selected from NH 2 , NH(CIA aliphatic), N(CI4 aliphatic) 2 , halogen, Cia aliphatic, OH, O(C 14 aliphatic), NO 2 , CN,

CO

2 H, CO2(CIA aliphatic), O(halo CI4 aliphatic), or halo(CI4 aliphatic), wherein each of the foregoing C.4aliphatic groups of R* is unsubstituted. 6 [00221 Optional substituents on the nitrogen of a non-aromatic heterocyclic ring are selected from -R*, -N(R*) 2 , -C(O)R*, -CO 2 R*, -C(O)C(O)R*, -C(O)CH 2 C(O)R*, -SO 2 R+,

-SO

2

N(R+)

2 , -C(=S)N(R*) 2 , -C(=NH)-N(R*) 2 , or -NR*SO 2 R+; wherein R* is hydrogen, an optionally substituted CI- 6 aliphatic, optionally substituted phenyl, optionally substituted -O(Ph), optionally substituted -CH 2 (Ph), optionally substituted -(CH 2 )i- 2 (Ph); optionally substituted -CH=CH(Ph); or an unsubstituted 5-6 membered heteroaryl or heterocyclic ring having one to four heteroatoms independently selected from oxygen, nitrogen, or sulfur, or, notwithstanding the definition above, two independent occurrences of R*, on the same substituent or different substituents, taken together with the atom(s) to which each R+ group is bound, form a 5-8-membered heterocyclyl, aryl, or heteroaryl ring or a 3-8-membered cycloalkyl ring having 0-3 heteroatoms independently selected from nitrogen, oxygen, or sulfur. Optional substituents on the aliphatic group or the phenyl ring of R* are selected from NH 2 ,

NH(C

14 aliphatic), N(C1A aliphatic) 2 , halogen, C1A aliphatic, OH, O(CA aliphatic), NO 2 , CN, CO2H, CO2(CI aliphatic), O(halo C1A aliphatic), or halo(C14 aliphatic), wherein each of the foregoing C1A aliphatic groups of R+ is unsubstituted. [00231 The term "alkylidene chain" refers to a straight or branched carbon chain that may be fully saturated or have one or more units of unsaturation and has two points of attachment to the rest of the molecule. 100241 As detailed above, in some embodiments, two independent occurrences of R' (or R+, or any other variable similarly defined herein), are taken together together with the atom(s) to which each variable is bound to form a 5-8-membered heterocyclyl, aryl, or heteroaryl ring or a 3-8-membered cycloalkyl ring having 0-3 heteroatoms independently selected from nitrogen, oxygen, or sulfur. Exemplary rings that are formed when two independent occurrences of R' (or R+, or any other variable similarly defined herein) are taken together with the atom(s) to which each variable is bound include, but are not limited to the following: a) two independent occurrences of R 0 (or R*, or any other variable similarly defined herein) that are bound to the same atom and are taken together with that atom to form a ring, for example, N(R) 2 , where both occurrences of R' are taken together with the nitrogen atom to form a piperidin-I-yl, piperazin-1-yl, or morpholin-4-yl group; and b) two independent occurrences of R 0 (or R+, or any other variable similarly defined herein) that are bound to different atoms and are taken together with both of those atoms to form a ring, for example where a phenyl group is ORO substituted with two occurrences of OR' \a , these two occurrences of R' are taken 7 together with the oxygen atoms to which they are bound to form a fused 6-membered oxygen containing ring: \aO . It will be appreciated that a variety of other rings can be formed when two independent occurrences of R' (or R+, or any other variable similarly defined herein) are taken together with the atom(s) to which each variable is bound and that the examples detailed above are not intended to be limiting. [00251 Unless otherwise stated, structures depicted herein are also meant to include all isomeric (e.g., enantiomeric, diastereomeric, and geometric (or conformational)) forms of the structure; for example, the R and S configurations for each asymmetric center, (Z) and (E) double bond isomers, and (Z) and (E) conformational isomers. Therefore, single stereochemical isomers as well as enantiomeric, diastereomeric, and geometric (or conformational) mixtures of the present compounds are within the scope of the invention. Unless otherwise stated, all tautomeric forms of the compounds of the invention are within the scope of the invention. Additionally, unless otherwise stated, structures depicted herein are also meant to include compounds that differ only in the presence of one or more isotopically enriched atoms. For example, compounds having the present structures except for the replacement of hydrogen by deuterium or tritium, or the replacement of a 1 2 C carbon by a 1 3 C or 1 4 C carbon are within the scope of this invention. Such compounds are useful, for example, as analytical tools or probes in biological assays. 100261 Description of Compounds of the Invention [00271 The invention provides a compound of formula I:

H

2 N A: N N HN RX (I) or a pharmaceutically acceptable salt, derivative or prodrug thereof, wherein: A is N or CR'; R' is H, halogen or a C1.

6 alkyl; Rx is selected from 8 N N N N (N C) ; N Hac 0 CH 3 H 7 7N N N R'N O R'N OR'N O N N N R' OR' N R R; RY is selected from N N N N N 0 N N N N N R N O N H 3 C CH 3 R O R" O -I - x each occurrence of R is independently selected from hydrogen or a CI.

6 aliphatic group optionally substituted with J or J'; and R' is independently selected from hydrogen or a group selected from Ci.

8 aliphatic optionally substituted with up to three occurrences of J or J', C 6

-

10 aryl optionally substituted with up to three occurrences of J, a heteroaryl ring having 5-10 ring atoms optionally substituted with up to three occurrences of J, or a heterocyclyl ring having 3-10 ring atoms optionally substituted with up to three occurrences of J or J, or wherein R and R' taken together, form a 5-8 membered cycloalkyl, heterocyclyl, aryl, or heteroaryl ring having 0-3 heteroatoms independently selected from nitrogen, oxygen, or sulfur, each ring being optionally and independently substituted with up to three occurrences of J; each occurrence of R" is independently selected from hydrogen or a group selected from C .

8 aliphatic optionally substituted with up to three occurrences of J or J', C 6

.

10 aryl optionally substituted with up to three occurrences of J, a heteroaryl ring having 5-10 ring atoms optionally substituted with up to three occurrences of J, or a heterocyclyl ring having 3-10 ring atoms optionally substituted with up to three occurrences of J or J', or wherein R and R" taken together, form a 5-8 membered cycloalkyl, heterocyclyl, aryl, or heteroaryl ring having 0-3 9 heteroatoms independently selected from nitrogen, oxygen, or sulfur, each ring being optionally and independently substituted with up to three occurrences of J; each occurrence of J is independently selected from halogen; -R*; -OR*; -SR*; 1,2 methylenedioxy; 1,2-ethylenedioxy; phenyl (Ph) optionally substituted with R'; -O(Ph) optionally substituted with R'; -(CH 2

)

1

-

2 (Ph) optionally substituted with R'; -CH=CH(Ph) optionally substituted with R'; -NO 2 ; -CN; -N(R 0

)

2 ; -NR*C(O)R*; -NR*C(S)R*;

-NR*C(O)N(R*)

2 ; -NR*C(S)N(R*) 2 ; -NR*CO 2 R'; -NR*NR*C(O)R 0 ; -NR*NR*C(O)N(R*) 2 ;

-NR*NR*CO

2 R*; -C(O)C(O)R*; -C(O)C(O)OR*, -C(O)C(O)N(R*) 2 , -C(O)CH 2 C(O)R*; -C0 2 R'; -C(O)R*; -C(S)R*; -C(S)OR', -C(O)N(R*) 2 ; -C(S)N(R*) 2 ; -C(=NH)-N(R*) 2 ,

-OC(O)N(R*)

2 ; -OC(O)R 0 ; -C(O)N(OR*) R'; -C(NOR*) R'; -S(0) 2 R*; -S(0) 3 R*; -SO 2

N(R*)

2 ; -S(O)R*; -NR*SO 2

N(R')

2 ; -NR*SO 2 R*; -N(OR')R*; -C(=NH)-N(R*) 2 ; C(=NOR')R*;

(CH

2 )o- 2

NHC(O)R

0 ; -P(O) 2

R

0 ; -PO(R*) 2 ; -OPO(R) 2 ; or -P(O)(H)(OR*); wherein each independent occurrence of R* is selected from hydrogen, optionally substituted C 1

-

6 aliphatic, optionally substituted 5-6 membered heteroaryl or heterocyclic ring, optionally substituted phenyl (Ph); optionally substituted -O(Ph); optionally substituted

-(CH

2

)

1

-

2 (Ph); optionally substituted -CH=CH(Ph); or, two independent occurrences of R 0 , on the same substituent or different substituents, taken together with the atom(s) to which each R* group is bound, form a 5-8-membered heterocyclyl, aryl, or heteroaryl ring or a 3-8-membered cycloalkyl ring having 0-3 heteroatoms independently selected from nitrogen, oxygen, or sulfur; wherein a substituent for an aliphatic group of R* is optionally substituted heteroaryl, optionally substituted, heterocyclic, NH 2 , NH(CI- 6 aliphatic), N(CI- 6 aliphatic) 2 , halogen, CI-6 aliphatic, OH, O(CI.

6 aliphatic), NO 2 , CN, CO 2 H, CO 2 (Ci- 6 aliphatic), O(halo CI.

6 aliphatic), or halo(CI.

6 aliphatic), wherein each of these CI.

6 aliphatic groups of R* is unsubstituted; wherein a substituent for a phenyl, heteroaryl or heterocyclic group of R' is CI.

6 aliphatic, NH 2 , NH(CI.

4 aliphatic), N(Ci- 6 aliphatic) 2 , halogen, Ci- 6 aliphatic, OH, O(CI- 6 aliphatic), NO 2 , CN, CO 2 H, CO 2

(CI.

6 aliphatic), O(halo CI.

6 aliphatic), or halo(Ci.

6 aliphatic), wherein each of these C 1

.

6 aliphatic groups of R* is unsubstituted; each occurrence of J' is independently selected from =0, =S, =NNHR*, =NN(R*) 2 , =NNHC(O)R*, =NNHCO 2 (alkyl), =NNHSO 2 (alkyl), or =NR*, where each R* is independently selected from hydrogen or an optionally substituted CI- 6 aliphatic; wherein an aliphatic group of R' is optionally substituted with NH 2 , NH(CA aliphatic), N(C14 aliphatic) 2 , halogen, C1A 10 aliphatic, OH, O(CIA aliphatic), NO 2 , CN, CO 2 H, CO2(CIA aliphatic), O(halo Ci.

4 aliphatic), or halo(C 1 . aliphatic), wherein each of the ClAaliphatic groups of R' is unsubstituted. [00281 In certain embodiments, Rx is selected from (N )N N (N R'N O R' N OR'N O N N N R' OR' R' N,R' O«R" O'OR" O N'R" R [00291 In certain embodiments of the invention, Ry is N N N N).. H N '-N N H 3 C N H 3 RO o 0 "R" R 00 [00301 In certain embodiments, A is N. 10031] In other embodiments, A is CR 2 . In further embodiments, A is CH. R'N O R'N O R'N O [00321 In some embodiments, Rx is selected from R' OR' R' N R'. In further embodiments, R' is a C 1 6 aliphatic, phenyl or a 5-8 membered heteroaryl group, wherein R' is optionally substituted with up to one occurrence of J. In further embodiments, R' is a C 1

.

6 aliphatic group or phenyl, wherein R' is optionally substituted with up to one occurrence of J, wherein J is -COOR', -ORO, R' or -CF 3 , and wherein R' is a C 1 3 aliphatic group. In still further embodiments, R' is methyl, ethyl, propyl, isopropyl, -C-1 2 -isopropyl, butyl, t-butyl, -CH 2 -t-butyl or cyclohexyl, wherein R' is optionally substituted with -COOR, -ORO or R 0 . In certain embodiments, R is hydrogen or methyl. (N) KN) (N) N N N O R"O OR"O N' [0033] In some embodiments, Rx is selected from R . In further embodiments, R" is independently selected from a C 1

.

6 aliphatic group, phenyl or a 5-8 membered heterocycle group, wherein R" is optionally substituted with up to one occurrence of J. In further embodiments, R" is independently selected from a C 1

-

6 aliphatic group or phenyl, wherein R" is optionally substituted with up to one occurrence of J, wherein J is selected from 11 halogen, -CF 3 , -CN, -COOR', -COR or -OR, wherein R' is a C 1

.

3 aliphatic group. In still further embodiments, R" is methyl, ethyl, propyl, isopropyl, -CH 2 -isopropyl, butyl, t-butyl or

-CH

2 -t-butyl, wherein R" is optionally substituted with -CN, -COOR 0 or -OR4. In certain embodiments, R is hydrogen or methyl. [00341 Specific embodiments of RX are depicted in the compounds in Table 1. N N N R" -OR"N N [00351 In some embodiments, Ry is selected from R or

H

3 C N CH 3 In further embodiments, R" is independently selected from a C 1

-

6 aliphatic group, phenyl or a 5-8 membered heterocycle group, wherein R" is optionally substituted with up to one occurrence of J. In further embodiments, R" is independently selected from a Ci-6 aliphatic group or phenyl, wherein R" is optionally substituted with up to one occurrence of J, wherein J is selected from halogen, -CF 3 , -CN, -COOR, -COR or -OR 0 , wherein R 0 is a C 1

.

3 aliphatic group. In still further embodiments, R" is methyl, ethyl, propyl, isopropyl, -CH 2 isopropyl, butyl, t-butyl or -CH 2 -t-butyl, wherein R" is optionally substituted with -CN, -COOR'or -OR. In certain embodiments, R is hydrogen or methyl. 100361 Specific embodiments of Ry are depicted in the compounds in Table 1. 10037] Representative examples of compounds of formula I are set forth in Table 1. 12 [00381 Table 1. Examples of Compounds of Formula 1: Compound Cmpd # N 4 01 Compound Cmpd# H 2 N 4 N N 00 144 Compound Cmpd # (I-#)

N

2 N N ~ '~"~- N 5 N 0 N~CN N

N

2 N N N N 6 0 N N 0 15 Compound Cmpd # NN 71 Compound Cmpd# NN NN r N r >~IJ N10 17 Compound Cmpd # (I-#) NN 4 2 4 0 N 14N NCH 182 Compound Cmpd # s4 2 N N H N 13 4N N 14 19 Compound Cmpd # 14 2 N N i N N 20 Compound Cmpd # CHI~ 0 17 0 424 14 N 21 Compound Cmnpd # N 19 42 02 4N N4 22 Compound Cmpd# NN

N

2 21 HNN 00 2 3 Compound Cmpd # ____ ___ ____ ___ ____ ___ ____ ___ ___ (1-#) N 23 N| 0| 24 Compound Cmpd # 4NN NN $4 N 0 4, 25 C41 '4I N NN 0 26 N4 C 25 Compound Cmpd# NI-N '4 2 N N N0 'IN 27 4,C 4 N 4IN 28 _, 26 Compound Cmpd# ____ ___ ____ ___ ____ ___ ____ ___ ___ (I-#) 4 2 NI N' N 14N NN 29 N. o 42N 03 27 Compound Cmpd # '4 2 " NN 'N0 32N~ C4, 28N Compound Cmpd# H4 2 N 4N 33 N '0 NC CHI14 N 0 4

N

2 29 Compound Cmpd# ____ ___ ___ ___ ___ ____ ___ ___ ___ ___(I-#) 14 2 4 4 CHI 3 CH N cl) 14N 36

H

3 C N CH 30 Compound Cmpd # 37 CH ~I N N.38 C W, 31 Compound Cmpd# ~432 CompoundCmdI N 4 2 N NN 0 -I N - 42 33 Compound Cmpd# N ~4N 'N.4 C4 NN N- C HI 0 34 Compound Cmpd# 1N 45 y N, H N N 0 HN 46 H~C 0 35 Compound Cmpd# 4 2 N 4NNf:O 47 N NN 48 NHC 0 H 36 Compound Cmpd # N 49 NN N I HC~ N 0 14 N~Y

~I

2 37 Compound Cmpd #

N

2 N 0,0 4CNN N N H14 1 3 52 N 0 C4, 38 Compound Cmnpd # 353 Compound Cmpd# '4 2 N1 C' N'4 55 HCHI 4N C 1 56 40 Compound Cmpd# N N N NI HI '4 NCHI CN 57 CHI N 0 CHI N N N N4 2 'IN C'4 1 C1 58 N CH, N 0 41 Compound Cmpd# \a w C41 C43 59 N NCH3 N 42 Compound Cmpd #I CHI N 13 C ,61 C41 y N H 0 CHI 6 43 Compound Cmpd# NN N 0 0 C141

H

2 N 14 64 N 44 Compound Cmpd I .4 2 N N N 6 5 NN NNN CCHI H N 45 Compound Cmpd # (1-#) NCHI N 67 4. CHI H H W24N CHI N y 68 0C 4 46 Compound Cmpd # / N N~ N N~f?69 4 NC4 3 N N 0 C 14, H '4 4 2 N N ~ 70 0 C41 4 Compound Cmpd # 4 2 N C4 N 0 72 NN C' 0 2 CN 1 H 48 Compound Cmpd # 2 C4#) Yo C C 3 N CHI 4 N4 N K-( 14N r r H2 C41 O 4 49 Compound Cmpd # 2N CH CHI N 4 2 N CM I N 4 76

CH

1 50 Compound Cmpd II N N~f~O77 C4 1 CHI '44 N~I - ~ N78 NN C1 51 Compound Cmpd # 144

C

3 52 Compound Cmpd # 81 42N

CN

1 -4, 53 Compound Cmpd# WN C41 CN 3 N. o 83 N 0 CHIS 4 N N N~~? 84 44 CH CHI 0 C 54 Compound Cmpd # HNN N0 N 85 ~4 N 55 Compound Cmpd# '4 2 NI NN N4 N 1 y N~ N~ NN WNN 0 H 1 C 88 N N N4 56 Compound Cmpd # (I-#) N 89 N 90 4N C 57 Compound (I-#) N 91 'N 0 NCH N 92 '44c 58 Compound Cmpd# NN N N 93 N. 0 0 94 HN 0 C43 59 Compound Cmpd # NN 11 2 N NN N HCN 4 2 M NN HN N. o NC 96 N 60 Compound Cmpd#4 NN NN 97 / II 4N H~C 98 0 CH N

C

0 CH, 61 Compound Cmpd # c 141 C4 3 CN. CN N4h 99 N O 42 C% C41 c 4, 4,C C41 62 Compound Cmpd# (I-#l) cwl 0 N N lc L42N4 4 2 101 Nk C4 I-C4 NN N 102 0 63 Compound Cmpd # C'4 1 0 CH N2 N 4 103 4C0 N CHI N N 4 2 N 104 0 64 Compound Cmpd# 4H2 NNN N4 C4 1

NN

2 , N) N 4, 4c 106 N 4 65 Compound Cmpd# NH2 N 4,C .4C 107 N 4 N ,C

N

2 A N \/ N WC C 108 C, 66 Compound Cmpd ft

NN

2 NCN4 HNN 10 C41

NN

2 , 67 Compound Cmpd # (I-N N'41 N~K \/ $42 C4 NN 0 0N 4 CHI 68 Compound Cmpd#

CHI

H C4 -4, 113

KIC

0 CH 114 659 Compound Cmpd # NN C4 115 0 4 C4 1 N 70 Compound Cmpd# 7117 WN C1/ C3 1 NN 714 Compound Cmpd # 4c 0N 119 Ic41 4 1 C CHI c C 1 120 0 N 1 I3 0 N| 72 Compound Cmpd # Hc~c 4N 122 0 14 73N Compound Cmpd # N// 0 44 ), N 4H 1 24 Na 4 0 74 Compound Cmpd 4 4 2 N NN NN 04 125 Ny N CH 126 '44 75 Compound Cmpd# >-C41 127 44 )a4 0 o / N N Hc )z3P 4 3 C 128 76 Compound Cmpd # N' N N129 W 4 N'041 130 77 Compound Cmpd# N N N' N 131 HN NN N N N~ C41 132 ~CHI NICHI 78 Compound Cmpd # NN N' NN 'CHI N 0 0 133 '134 79 Compound Cmpd# 44 N. ~ 0135 80 Compound (I-#) Nd NN N C 137 4 2 N) NN 0 138 C41 81 Compound Cmpd # N'4 2 NN N~c 2~O139 NH I C) 82 2 Compound Cmpd # 4I 2 H NN N 4 0 4H 4 14 Nx'N \I x 14N HC 4, 142 _0 NCH 83 Compound Cmpd # N4N N 4 (-N 4,C 143 IC) \aN 0 84 Compound Cmpd # N 0 \r ~ \ s, 44 145 ON 4N 146 0 85 Compound Cmpd# 4 2 N 44 147 0 N 42 N N 0 N ,NCu 3 148 0 86 Compound Cmpd # NN N C 14 C4, N. 0 C4 87 Compound Cmpd# C64 151 0, qz N N152 s C1 88 Compound Cmpd# N 153 0 15 89 Compound Cmpd#4 C'4 1 155 0/ 0 MN z 0/ 156 90 Compound Crnpd # 0 157 4, 4 (7) HN / 158 N 91 Compound Cmpd # N 142 N 159 N C160 0 92 2 Compound Cmpd# CHI# HNN 4,C 162 (N N N 1 c 93 2 Compound Cmpd # 1I-#) '44 'ii. \ N 163 4S.

H.:rJ-0 WN (7)4 N 4,Ci Nh94 Compound Cmpd# NN N N /, 165 C)4 N 16 c HI 95 Compound Cmpd# NN NN 167 0 N14 2 _ HN N N16 NN HIC ~4, 96 Compound Cmpd # 4 N O=S 169 N ;rN 717 CN4 97 Compound Cmpd# 14 2 " NN N 172 98 Compound Cmpd # 4N 4 H 173 I- 0 0 CH 174 444 99 Compound Cmpd# (I-#) eH, 175 '4N1 N 7NN eN I 176 'H43 CH, 100391 General Synthetic Methodology: [00401 The compounds of this invention may be prepared in general by methods known to those skilled in the art for analogous compounds, by methods as illustrated by the general schemes below, and by the preparative examples that follow. The processes for preparing the compounds of this invention are as described in the schemes and examples. In the schemes, the variables are as defined in the compounds (e.g., formula I) herein or are readily recognized by referring to those compounds. 100 100411 Scheme 7 depicts the synthesis of certain exemplary compounds where Ar' and Ar 2 is substituted.

NH

2 NCj"

NH

2 NNR N/N N N HN HNA B HN N NH 2 N H R N/N N _'R H N-R' NH N R' N//RNHN C N N'R HN D H

NH

2 E N E'NH .- .RN R' N/N N N/ N" N~ HN D NH 2 HN N HNN N-R' X-.. R' C N/'N NN N~O N'N= H R' [00421 General conditions: solvent, base, appropriate coupling agent, e.g.: A. DMF, DIEA, RCOCI; B. DMF, IEA, isocyanate; C. DMF, DIEA, chloroformate D. DMF, DIEA, IS02R; E. iPrOH, alkyl halide, heat. [00431 Scheme 7 depicts a route to compounds of this invention wherein an Ar' is substituted with an amine derivative, specifically where R 2 is (T),Ar', and Ar' is substituted with an amine derivative. In Scheme 7, the amine group is reacted under standard coupling conditions to provide an amine derivative. It should be understood that the depicted synthesis could be modified to also provide other amine derivatives. Furthermore, coupling conditions other than those depicted could be used. Such methods are well-known to skilled practitioners (see, e.g., Greene or Greene & Wutz, Protective Groups in Organic Synthesis; WO 01/81330). It should be understood that the conditions should typically be chosen to be compatible with (i.e., unreactive to) the remaining substituents (e.g., the -NR'R 2 ). 101 100441 Scheme 1: Route to diamino triazole compounds. n=1,2 N N + HN N-J(Rj CH3CN N-: 'IN n=1,2 DIEA/DCM NH DIEA R '-( 12 NH R3 ACI N'N n=1,2 N n=1,2 CI N~'~ 22 HN' N I ~~R yN

NH

2 yNO

R

2

R

3 3 R 2

R

3 0 l 0 H Ni-PrO H H l N z NC , N ~ ____c <~N NC H~o K.NCfN NHBoc 4 H N~z N n12H 2 N N'-N n12R +~~~ HN I~~R NY~~ YC' NH o NH N 0 -N1 ly~Omicrowave

HNR

2 R N C ' HRo R 3 2 8 d e g r e e /N R 2 R R2 R3 6 min N Nz N n1'2NHBoc TFAIDCM //N '4 ~ N IK(R, 5 __;:____N ( N HN 0R 2

R

3

NH

2 6 102 [0045] Scheme 2: Route to derivatives of diamino triazole compounds.

H

2 N NAN N R1 H N N O H N

R

2

R

3 Method A -Method B H2N N N n=1,2 NH 2

H

2 N N N n=1,2 N N N R1 N N N N R1 NO N NO HN

R

2

R

3 Method C HN

R

2

R

3 - 0 - 0 R4 H N-R 5

H

2 N NN 1 H H, N ) A N O N' I H N

R

2

R

3

-

0 HN4

OR

6 Method A: DMF, DIEA, R.T., carboxylate chloride Method B: DMF, DIEA, R.T., isocynate Method C: DMF, DIEA, R.T., chloroformate 103 [00461 Scheme 3: Route to diamino triazole compounds. Hz 2 N N H2

H

2 N N CI N N NR1 N ,N , I N a N b R2 HN CI HN ' HN N H 2 R O -0 - 0 HN HN

H

2 N N ' R1

H

2 N R1 N I METHOD N I I c )z:N R2 A N R2 HN HN 3 R3O

NH

2 METHOD HN- R METHOD

H

2 N N H 2 N //' I N Rj N N Rj N N , I N R2 N R2 HN HN O R 3 0 0

HN-

1

HN

R N-R H (a) N-cyano-N'-aryl-O-phenylisourea, NMP, DIEA, MW, 160-220 'C, 6-15 min; (b) HNRi

R

2 , NMP, M W, 220-250 'C, 6-15 min; (c) 6N HCl, 95 'C; METHOD A: ClCO 2 R (chloroformate), DIEA, DMF; METHOD B: OCN-R (isocyanate), DIEA, DMF; METHOD C:

RCO

2 H (carboxylic acid), DCC, DCM, or RCOCI (acid chloride), DIEA or pyridine, DMF 100471 Another general route to compounds of this invention is depicted in Scheme 3. Although specific reagents are depicted in Scheme 3, skilled practitioners would realize that other steps and reagents could be used to carry out the depicted synthesis. Schemes 4 and 5 below depict this general scheme more specifically. 100481 Although certain exemplary embodiments are depicted and described above and herein, it will be appreciated that the compounds of the invention can be prepared according to 104 the methods described generally above using appropriate starting materials by methods generally available to one of ordinary skill in the art. 100491 Uses, Formulations and Administration 100501 Pharmaceutically acceptable compositions 100511 As discussed above, the present invention provides compounds that are inhibitors of protein kinases, and thus the present compounds are useful for the treatment of diseases, disorders, and conditions including, but not limited to, allergic disorders, proliferative disorders, autoimmune disorders, conditions associated with organ transplant, inflammatory disorders, immunologically mediated disorders, viral diseases, or destructive bone disorders (such as bone resorption disorders). Accordingly, in another aspect of the present invention, pharmaceutically acceptable compositions are provided, wherein these compositions comprise any of the compounds as described herein, and optionally comprise a pharmaceutically acceptable carrier, adjuvant or vehicle. In certain embodiments, these compositions optionally further comprise one or more additional therapeutic agents. 100521 It will also be appreciated that certain of the compounds of present invention can exist in free form for treatment, or where appropriate, as a pharmaceutically acceptable derivative thereof. According to the present invention, a pharmaceutically acceptable derivative includes, but is not limited to, pharmaceutically acceptable salts, esters, salts of such esters, or any other adduct or derivative which upon administration to a patient in need is capable of providing, directly or indirectly, a compound as otherwise described herein, or a metabolite or residue thereof. 100531 As used herein, the term "pharmaceutically acceptable salt" refers to those salts which are, within the scope of sound medical judgement, suitable for use in contact with the tissues of humans and lower animals without undue toxicity, irritation, allergic response and the like, and are commensurate with a reasonable benefit/risk ratio. A "pharmaceutically acceptable salt" means any non-toxic salt or salt of an ester of a compound of this invention that, upon administration to a recipient, is capable of providing, either directly or indirectly, a compound of this invention or a metabolite or residue thereof that inhibits the kinase of interest, including Aurora-2, Flt3, KDR, JAK2 and JAK3. In particular embodiments, the compound or pharmaceutically acceptable salt thereof inhibits JAK2 or JAK3. [00541 Pharmaceutically acceptable salts are well known in the art. For example, S. M. Berge et al., describe pharmaceutically acceptable salts in detail in J Pharmaceutical Sciences, 1977, 66, 1-19, incorporated herein by reference. Pharmaceutically acceptable salts of the compounds of this invention include those derived from suitable inorganic and organic acids 105 and bases. Examples of pharmaceutically acceptable, nontoxic acid addition salts are salts of an amino group formed with inorganic acids such as hydrochloric acid, hydrobromic acid, phosphoric acid, sulfuric acid and perchloric acid or with organic acids such as acetic acid, oxalic acid, maleic acid, tartaric acid, citric acid, succinic acid or malonic acid or by using other methods used in the art such as ion exchange. 100551 Other pharmaceutically acceptable salts include adipate, alginate, ascorbate, aspartate, benzenesulfonate, benzoate, bisulfate, borate, butyrate, camphorate, camphor sulfonate, citrate, cyclopentanepropionate, digluconate, dodecylsulfate, ethanesulfonate, formate, fumarate, glucoheptonate, glycerophosphate, gluconate, hemisulfate, heptanoate, hexanoate, hydroiodide, 2-hydroxy-ethanesulfonate, lactobionate, lactate, laurate, lauryl sulfate, malate, maleate, malonate, methanesulfonate, 2-naphthalenesulfonate, nicotinate, nitrate, oleate, oxalate, palmitate, pamoate, pectinate, persulfate, 3-phenylpropionate, phosphate, picrate, pivalate, propionate, stearate, succinate, sulfate, tartrate, thiocyanate, p-toluenesulfonate, undecanoate, valerate salts, and the like. Salts derived from appropriate bases include alkali metal, alkaline earth metal, ammonium and N'(C 1 4 alkyl) 4 salts. 100561 This invention also envisions the quaternization of any basic nitrogen-containing groups of the compounds disclosed herein. Water or oil-soluble or dispersable products may be obtained by such quaternization. Representative alkali or alkaline earth metal salts include sodium, lithium, potassium, calcium, magnesium, and the like. Further pharmaceutically acceptable salts include, when appropriate, nontoxic ammonium, quaternary ammonium, and amine cations formed using counterions such as halide, hydroxide, carboxylate, sulfate, phosphate, nitrate, loweralkyl sulfonate and aryl sulfonate. 100571 As described above, the pharmaceutically acceptable compositions of the present invention additionally comprise a pharmaceutically acceptable carrier, adjuvant, or vehicle, which, as used herein, includes any and all solvents, diluents, or other liquid vehicle, dispersion or suspension aids, surface active agents, isotonic agents, thickening or emulsifying agents, preservatives, solid binders, lubricants and the like, as suited to the particular dosage form desired. Remington's Pharmaceutical Sciences, Sixteenth Edition, E. W. Martin (Mack Publishing Co., Easton, Pa., 1980) discloses various carriers used in formulating pharma ceutically acceptable compositions and known techniques for the preparation thereof. Except insofar as any conventional carrier medium is incompatible with the compounds of the invention, such as by producing any undesirable biological effect or otherwise interacting in a deleterious manner with any other component(s) of the pharmaceutically acceptable composition, its use is contemplated to be within the scope of this invention. 106 [00581 Some examples of materials which can serve as pharmaceutically acceptable carriers include, but are not limited to, ion exchangers, alumina, aluminum stearate, lecithin, serum proteins, such as human serum albumin, buffer substances such as phosphates, glycine, sorbic acid, or potassium sorbate, partial glyceride mixtures of saturated vegetable fatty acids, water, salts or electrolytes, such as protamine sulfate, disodium hydrogen phosphate, potassium hydrogen phosphate, sodium chloride, zinc salts, colloidal silica, magnesium trisilicate, polyvinyl pyrrolidone, polyacrylates, waxes, polyethylene-polyoxypropylene-block polymers, wool fat, sugars such as lactose, glucose and sucrose; starches such as corn starch and potato starch; cellulose and its derivatives such as sodium carboxymethyl cellulose, ethyl cellulose and cellulose acetate; powdered tragacanth; malt; gelatin; talc; excipients such as cocoa butter and suppository waxes; oils such as peanut oil, cottonseed oil; safflower oil; sesame oil; olive oil; corn oil and soybean oil; glycols; such a propylene glycol or polyethylene glycol; esters such as ethyl oleate and ethyl laurate; agar; buffering agents such as magnesium hydroxide and aluminum hydroxide; alginic acid; pyrogen-free water; isotonic saline; Ringer's solution; ethyl alcohol, and phosphate buffer solutions, as well as other non-toxic compatible lubricants such as sodium lauryl sulfate and magnesium stearate, as well as coloring agents, releasing agents, coating agents, sweetening, flavoring and perfuming agents, preservatives and antioxidants can also be present in the composition, according to the judgment of the formulator. [00591 Uses of Compounds and Pharmaceutically acceptable compositions 100601 In yet another aspect, a method for the treatment or lessening the severity of allergic disorders, proliferative disorders, autoimmune disorders, conditions associated with organ transplant, inflammatory disorders, immunologically mediated disorders, viral diseases, or destructive bone disorders(such as bone resorption disorders) is provided comprising administering an effective amount of a compound, or a pharmaceutically acceptable composition comprising a compound to a subject in need thereof. In certain embodiments of the present invention an "effective amount" of the compound or pharmaceutically acceptable composition is that amount effective for for treating or lessening the severity of the disease, disorder, or condition of interest. The compounds and compositions, according to the method of the present invention, may be administered using any amount and any route of administration effective for treating or lessening the severity of the disease, disorder, or condition of interest. The exact amount required will vary from subject to subject, depending on the species, age, and general condition of the subject, the severity of the infection, the particular agent, its mode of administration, and the like. The compounds of the invention are preferably formulated in dosage unit form for ease of administration and uniformity of dosage. The expression "dosage 107 unit form" as used herein refers to a physically discrete unit of agent appropriate for the patient to be treated. It will be understood, however, that the total daily usage of the compounds and compositions of the present invention will be decided by the attending physician within the scope of sound medical judgment. The specific effective dose level for any particular patient or organism will depend upon a variety of factors including the disorder being treated and the severity of the disorder; the activity of the specific compound employed; the specific composition employed; the age, body weight, general health, sex and diet of the patient; the time of administration, route of administration, and rate of excretion of the specific compound employed; the duration of the treatment; drugs used in combination or coincidental with the specific compound employed, and like factors well known in the medical arts. The term "patient", as used herein, means an animal, preferably a mammal, and most preferably a human. 100611 The pharmaceutically acceptable compositions of this invention can be administered to humans and other animals orally, rectally, parenterally, intracisternally, intravaginally, intraperitoneally, topically (as by powders, ointments, or drops), bucally, as an oral or nasal spray, or the like, depending on the severity of the infection being treated. In certain embodiments, the compounds of the invention may be administered orally or parenterally at dosage levels of about 0.01 mg/kg to about 50 mg/kg and preferably from about 1 mg/kg to about 25 mg/kg, of subject body weight per day, one or more times a day, to obtain the desired therapeutic effect. 100621 Liquid dosage forms for oral administration include, but are not limited to, pharmaceutically acceptable emulsions, microemulsions, solutions, suspensions, syrups and elixirs. In addition to the active compounds, the liquid dosage forms may contain inert diluents commonly used in the art such as, for example, water or other solvents, solubilizing agents and emulsifiers such as ethyl alcohol, isopropyl alcohol, ethyl carbonate, ethyl acetate, benzyl alcohol, benzyl benzoate, propylene glycol, 1,3-butylene glycol, dimethylformamide, oils (in particular, cottonseed, groundnut, corn, germ, olive, castor, and sesame oils), glycerol, tetrahydrofurfuryl alcohol, polyethylene glycols and fatty acid esters of sorbitan, and mixtures thereof. Besides inert diluents, the oral compositions can also include adjuvants such as wetting agents, emulsifying and suspending agents, sweetening, flavoring, and perfuming agents. 100631 Injectable preparations, for example, sterile injectable aqueous or oleaginous suspensions may be formulated according to the known art using suitable dispersing or wetting agents and suspending agents. The sterile injectable preparation may also be a sterile injectable solution, suspension or emulsion in a nontoxic parenterally acceptable diluent or solvent, for example, as a solution in 1,3-butanediol. Among the acceptable vehicles and solvents that may 108 be employed are water, Ringer's solution, U.S.P. and isotonic sodium chloride solution. In addition, sterile, fixed oils are conventionally employed as a solvent or suspending medium. For this purpose any bland fixed oil can be employed including synthetic mono- or diglycerides. In addition, fatty acids such as oleic acid are used in the preparation of injectables. 100641 The injectable formulations can be sterilized, for example, by filtration through a bacterial-retaining filter, or by incorporating sterilizing agents in the form of sterile solid compositions which can be dissolved or dispersed in sterile water or other sterile injectable medium prior to use. 100651 In order to prolong the effect of a compound of the present invention, it is often desirable to slow the absorption of the compound from subcutaneous or intramuscular injection. This may be accomplished by the use of a liquid suspension of crystalline or amorphous material with poor water solubility. The rate of absorption of the compound then depends upon its rate of dissolution that, in turn, may depend upon crystal size and crystalline form. Alternatively, delayed absorption of a parenterally administered compound form is accomplished by dissolving or suspending the compound in an oil vehicle. Injectable depot forms are made by forming microencapsule matrices of the compound in biodegradable polymers such as polylactide-polyglycolide. Depending upon the ratio of compound to polymer and the nature of the particular polymer employed, the rate of compound release can be controlled. Examples of other biodegradable polymers include poly(orthoesters) and poly(anhydrides). Depot injectable formulations are also prepared by entrapping the compound in liposomes or microemulsions that are compatible with body tissues. 100661 Compositions for rectal or vaginal administration are preferably suppositories which can be prepared by mixing the compounds of this invention with suitable non-irritating excipients or carriers such as cocoa butter, polyethylene glycol or a suppository wax which are solid at ambient temperature but liquid at body temperature and therefore melt in the rectum or vaginal cavity and release the active compound. 100671 Solid dosage forms for oral administration include capsules, tablets, pills, powders, and granules. In such solid dosage forms, the active compound is mixed with at least one inert, pharmaceutically acceptable excipient or carrier such as sodium citrate or dicalcium phosphate and/or a) fillers or extenders such as starches, lactose, sucrose, glucose, mannitol, and silicic acid, b) binders such as, for example, carboxymethylcellulose, alginates, gelatin, polyvinylpyrrolidinone, sucrose, and acacia, c) humectants such as glycerol, d) disintegrating agents such as agar--agar, calcium carbonate, potato or tapioca starch, alginic acid, certain silicates, and sodium carbonate, e) solution retarding agents such as paraffin, f) absorption 109 accelerators such as quaternary ammonium compounds, g) wetting agents such as, for example, cetyl alcohol and glycerol monostearate, h) absorbents such as kaolin and bentonite clay, and i) lubricants such as talc, calcium stearate, magnesium stearate, solid polyethylene glycols, sodium lauryl sulfate, and mixtures thereof. In the case of capsules, tablets and pills, the dosage form may also comprise buffering agents. [00681 Solid compositions of a similar type may also be employed as fillers in soft and hard-filled gelatin capsules using such excipients as lactose or milk sugar as well as high molecular weight polyethylene glycols and the like. The solid dosage forms of tablets, dragees, capsules, pills, and granules can be prepared with coatings and shells such as enteric coatings and other coatings well known in the pharmaceutical formulating art. They may optionally contain opacifying agents and can also be of a composition that they release the active ingredient(s) only, or preferentially, in a certain part of the intestinal tract, optionally, in a delayed manner. Examples of embedding compositions that can be used include polymeric substances and waxes. Solid compositions of a similar type may also be employed as fillers in soft and hard-filled gelatin capsules using such excipients as lactose or milk sugar as well as high molecular weight polethylene glycols and the like. 100691 The active compounds can also be in micro-encapsulated form with one or more excipients as noted above. The solid dosage forms of tablets, dragees, capsules, pills, and granules can be prepared with coatings and shells such as enteric coatings, release controlling coatings and other coatings well known in the pharmaceutical formulating art. In such solid dosage forms the active compound may be admixed with at least one inert diluent such as sucrose, lactose or starch. Such dosage forms may also comprise, as is normal practice, additional substances other than inert diluents, e.g., tableting lubricants and other tableting aids such a magnesium stearate and microcrystalline cellulose. In the case of capsules, tablets and pills, the dosage forms may also comprise buffering agents. They may optionally contain opacifying agents and can also be of a composition that they release the active ingredient(s) only, or preferentially, in a certain part of the intestinal tract, optionally, in a delayed manner. Examples of embedding compositions that can be used include polymeric substances and waxes. 10070] Dosage forms for topical or transdermal administration of a compound of this invention include ointments, pastes, creams, lotions, gels, powders, solutions, sprays, inhalants or patches. The active component is admixed under sterile conditions with a pharmaceutically acceptable carrier and any needed preservatives or buffers as may be required. Ophthalmic formulation, ear drops, and eye drops are also contemplated as being within the scope of this 110 invention. Additionally, the present invention contemplates the use of transdermal patches, which have the added advantage of providing controlled delivery of a compound to the body. Such dosage forms can be made by dissolving or dispensing the compound in the proper medium. Absorption enhancers can also be used to increase the flux of the compound across the skin. The rate can be controlled by either providing a rate controlling membrane or by dispersing the compound in a polymer matrix or gel. [00711 As described generally above, the compounds of the invention are useful as inhibitors of protein kinases. In one embodiment, the compounds and compositions of the invention are inhibitors of one or more of Aurora-2, Flt3, KDR, JAK2 and JAK3. In certain preferred embodiments, these compounds are effective as inhibitors of JAK2 and JAK3. Thus, without wishing to be bound by any particular theory, the compounds and compositions are particularly useful for treating or lessening the severity of a disease, condition, or disorder where activation of one or more of the protein kinases, including Aurora-2, Flt3, KDR, JAK2 and JAK3 kinases, is implicated in the disease, condition, or disorder. When activation of the Aurora-2, Flt3, KDR, JAK2 and JAK3 kinases is implicated in a particular disease, condition, or disorder, the disease, condition, or disorder may also be referred to as "Aurora-2, Flt3, KDR, JAK2 or JAK3-mediated disease" or disease symptom. Accordingly, in another aspect, the present invention provides a method for treating or lessening the severity of a disease, condition, or disorder where activation or one or more protein kinase, including the Aurora-2, FIt3, KDR, JAK2 and JAK3 kinases is implicated in the disease state. 100721 The activity of a compound utilized in this invention as an inhibitor of a protein kinase, may be assayed in vitro, in vivo or in a cell line. In vitro assays include assays that determine inhibition of either the phosphorylation activity or ATPase activity of, e.g., activated Aurora-2, Flt3, KDR, JAK2 and JAK3. Alternate in vitro assays quantitate the ability of the inhibitor to bind to the protein kinase. Inhibitor binding may be measured by radiolabelling the inhibitor prior to binding, isolating the inhibitor/enzyme, complex and determining the amount of radiolabel bound. Alternatively, inhibitor binding may be determined by running a competition experiment where new inhibitors are incubated with, e.g., Aurora-2, Flt3, KDR, JAK2 and JAK3 bound to known radioligands. [00731 The term "measurably inhibit", as used herein means a measurable change in a kinase activity between a sample comprising a composition and a kinase and an equivalent sample comprising the kinase in the absence of the composition. [00741 The term "FLT-3-mediated disease", as used herein means any disease or other deleterious condition in which a FLT-3 family kinase is known to play a role. Such conditions I1 include, without limitation, hematopoietic disorders, in particular, acute-myelogenous leukemia (AML), acute-promyelocytic leukemia (APL), and acute lymphocytic leukemia (ALL). 100751 The term "JAK-mediated disease", as used herein means any disease or other deleterious condition in which a JAK family kinase, in particular JAK-3, is known to play a role. Such conditions include, without limitation, immune responses such as allergic or type I hypersensitivity reactions, asthma, autoimmune diseases such as transplant rejection, graft versus host disease, rheumatoid arthritis, amyotrophic lateral sclerosis, and multiple sclerosis, neurodegenerative disorders such as Familial amyotrophic lateral sclerosis (FALS), as well as in solid and hematologic malignancies such as leukemias and lymphomas. Conditions in which JAK2 play a role include myeloproliferative disorders, such as polycythemia vera, essential thrombocythemia, chronic idiopathic myelofibrosis, myeloid metaplasia with myelofibrosis, chronic myeloid leukemia, chronic myelomonocytic leukemia, chronic eosinophilic leukemia, hypereosinophilic syndrome and systematic mast cell disease. [00761 The term "AUR-mediated disease" or "AUR-mediated condition", as used herein, means any disease or other deleterious condition in which AUR protein kinase is known to play a role. Such conditions include, without limitation, allergic disorders, especially asthma. 10077] It will also be appreciated that the compounds and pharmaceutically acceptable compositions of the present invention can be employed in combination therapies, that is, the compounds and pharmaceutically acceptable compositions can be administered concurrently with, prior to, or subsequent to, one or more other desired therapeutics or medical procedures. The particular combination of therapies (therapeutics or procedures) to employ in a combination regimen will take into account compatibility of the desired therapeutics and/or procedures and the desired therapeutic effect to be achieved. It will also be appreciated that the therapies employed may achieve a desired effect for the same disorder (for example, an inventive compound may be administered concurrently with another agent used to treat the same disorder), or they may achieve different effects (e.g., control of any adverse effects). As used herein, additional therapeutic agents that are normally administered to treat or prevent a particular disease, or condition, are known as "appropriate for the disease, or condition, being treated". 100781 For example, chemotherapeutic agents or other anti-proliferative agents may be combined with the compounds of this invention to treat proliferative diseases and cancer. Examples of known chemotherapeutic agents include, but are not limited to, For example, other therapies or anticancer agents that may be used in combination with the inventive anticancer agents of the present invention include surgery, radiotherapy (in but a few examples, gamma.

112 radiation, neutron beam radiotherapy, electron beam radiotherapy, proton therapy, brachytherapy, and systemic radioactive isotopes, to name a few), endocrine therapy, biologic response modifiers (interferons, interleukins, and tumor necrosis factor (TNF) to name a few), hyperthermia and cryotherapy, agents to attenuate any adverse effects (e.g., antiemetics), and other approved chemotherapeutic drugs, including, but not limited to, alkylating drugs (mechlorethamine, chlorambucil, Cyclophosphamide, Melphalan, Ifosfamide), antimetabolites (Methotrexate), purine antagonists and pyrimidine antagonists (6-Mercaptopurine, 5 Fluorouracil, Cytarabile, Gemcitabine), spindle poisons (Vinblastine, Vincristine, Vinorelbine, Paclitaxel), podophyllotoxins (Etoposide, Irinotecan, Topotecan), antibiotics (Doxorubicin, Bleomycin, Mitomycin), nitrosoureas (Carmustine, Lomustine), inorganic ions (Cisplatin, Carboplatin), enzymes (Asparaginase), and hormones (Tamoxifen, Leuprolide, Flutamide, and Megestrol), GleevecTM, adriamycin, dexamethasone, and cyclophosphamide. For a more comprehensive discussion of updated cancer therapies see, http://www.nci.nih.gov/, a list of the FDA approved oncology drugs at http://www.fda.gov/cder/cancer/druglistframe.htm, and The Merck Manual, Seventeenth Ed. 1999, the entire contents of which are hereby incorporated by reference. 100791 Other examples of agents the inhibitors of this invention may also be combined with include, without limitation: treatments for Alzheimer's Disease such as Aricept* and Excelon*; treatments for Parkinson's Disease such as L-DOPA/carbidopa, entacapone, ropinrole, pramipexole, bromocriptine, pergolide, trihexephendyl, and amantadine; agents for treating Multiple Sclerosis (MS) such as beta interferon (e.g., Avonex* and Rebifo), Copaxone®, and mitoxantrone; treatments for asthma such as albuterol and Singulair*; agents for treating schizophrenia such as zyprexa, risperdal, seroquel, and haloperidol; anti-inflammatory agents such as corticosteroids, TNF blockers, IL-I RA, azathioprine, cyclophosphamide, and sulfasalazine; immunomodulatory and immunosuppressive agents such as cyclosporin, tacrolimus, rapamycin, mycophenolate mofetil, interferons, corticosteroids, cyclophosphamide, azathioprine, and sulfasalazine; neurotrophic factors such as acetylcholinesterase inhibitors, MAO inhibitors, interferons, anti-convulsants, ion channel blockers, riluzole, and anti Parkinsonian agents; agents for treating cardiovascular disease such as beta-blockers, ACE inhibitors, diuretics, nitrates, calcium channel blockers, and statins; agents for treating liver disease such as corticosteroids, cholestyramine, interferons, and anti-viral agents; agents for treating blood disorders such as corticosteroids, anti-leukemic agents, and growth factors; and agents for treating immunodeficiency disorders such as gamma globulin. 113 [0080] The amount of additional therapeutic agent present in the compositions of this invention will be no more than the amount that would normally be administered in a composition comprising that therapeutic agent as the only active agent. Preferably the amount of additional therapeutic agent in the presently disclosed compositions will range from about 50% to 100% of the amount normally present in a composition comprising that agent as the only therapeutically active agent. 100811 The compounds of this invention or pharmaceutically acceptable compositions thereof may also be incorporated into compositions for coating implantable medical devices, such as prostheses, artificial valves, vascular grafts, stents and catheters. Accordingly, the present invention, in another aspect, includes a composition for coating an implantable device comprising a compound of the present invention as described generally above, and in classes and subclasses herein, and a carrier suitable for coating said implantable device. In still another aspect, the present invention includes an implantable device coated with a composition comprising a compound of the present invention as described generally above, and in classes and subclasses herein, and a carrier suitable for coating said implantable device. 100821 Vascular stents, for example, have been used to overcome restenosis (re-narrowing of the vessel wall after injury). However, patients using stents or other implantable devices risk clot formation or platelet activation. These unwanted effects may be prevented or mitigated by pre-coating the device with a pharmaceutically acceptable composition comprising a kinase inhibitor. Suitable coatings and the general preparation of coated implantable devices are described in US Patents 6,099,562; 5,886,026; and 5,304,121. The coatings are typically biocompatible polymeric materials such as a hydrogel polymer, polymethyldisiloxane, polycaprolactone, polyethylene glycol, polylactic acid, ethylene vinyl acetate, and mixtures thereof. The coatings may optionally be further covered by a suitable topcoat of fluorosilicone, polysaccarides, polyethylene glycol, phospholipids or combinations thereof to impart controlled release characteristics in the composition. 100831 Another aspect of the invention relates to inhibiting a protein kinase (e.g., Aurora02, activity in a biological sample or a patient, which method comprises administering to the patient, or contacting said biological sample with a compound of formula I or a composition comprising said compound. The term "biological sample", as used herein, includes, without limitation, cell cultures or extracts thereof; biopsied material obtained from a mammal or extracts thereof; and blood, saliva, urine, feces, semen, tears, or other body fluids or extracts thereof. 114 100841 Inhibition of kinase activity, including Aurora-2, Flt3, KDR, JAK2 and JAK3 kinase activity, in a biological sample is useful for a variety of purposes that are known to one of skill in the art. Examples of such purposes include, but are not limited to, blood transfusion, organ transplantation, biological specimen storage, and biological assays. EXAMPLES [00851 Compounds of general formula I were prepared according to the general procedures described in the Schemes and Examples herein. [00861 Example 1. Preparation of 4-chloro-6-((3S,5R)-3,5-dimethylpiperazin- 1 yllpyrimidine (1) N 4 N CI N NH [00871 To a solution of 4,6-dichloropyrymidine (14.9 g, 100.0 mmol) in 150 ml anhydrous acetonitrile was added (2S,6R)-2,6-dimethylpiperazine (22.8 g, 200.0 mmol) portionwise over 10 min. The reaction was kept at room temperature using a water-bath and stirred for another 20 minutes. Solid precipitated out from solution during the course of reaction. Solid was removed by filtration. The filtrate was concentrated to an oily material. This material was dissolved in EtOAc (300 ml) and organic layer was washed with water (100mlx3). Organic layer was dried over NacSO 4 . Removal of solvent left an oil product as desired product confirmed by LC/MS (MS+1=227.1). This material was weighted at 22.lg (yield 97.6%). 100881 Example 2. Preparation of 1-((2S,6R)-4-(6-chloropyrimidin-4-yl)-2,6 dimethylpiperazin- I -yl)ethanone (2) N N CI N N O 2 [00891 To a solution of 4-chloro-6-((3S,5R)-3,5-dimethylpiperazin-1-yl)pyrimidine(1, 10.29 g, 45.4 mmol) and DIEA (8.80 g, 68.1 mmol. 1.50 equiv.) in 100 ml DCM was added acetyl chloride (4.03 ml, 56.7 mmol, 1.25 equiv.) at room temperature portionwise over 10 min. The reaction was stirred at room temperature for another 30 min. Aqueous NaHCO3 was added to the reaction and the organic layer was washed with NahCO3 (100 mlx2) followed by 115 saturated aqueous NaCl solution. The organic layer was dried over Organic layer was dried over NacSO 4 . Removal of solvent left a yellow oil. This oily material was triturated in diethyl ether to afford a white solid. The soid was collected by filtration and the washed with diethyl ether again. The solid was dried under vacuum and was weighted at 11.95 g. The yield is 98.2%. LC/MS (M+1=269.l). [00901 Example 3. Preparation of 3 N 1 N HN N

NH

2 N 0 3 [00911 To a solution of 1-((2S,6R)-4-(6-chloropyrimidin-4-yl)-2,6-dimethylpiperazin- 1 yl)ethanone (2, 9.61 g, 35.7 mmol) in 75 ml anhydrous THF was added hydrazine (5.72g, 5.60 ml, 178.8 mmol, 5.0 equiv.). Solid was precipitated out of the solution during the course of reaction. The reaction was stirred and refluxed overnight. The reaction was cooled to room temperature. The solid was collected filtration and was washed by cold methanol (25 mlx3) to get rid of excess hydrazine and its HC salt. The solid was dried under vacuum and was weighted at 8.95 g (83.3% yield). LC/MS (M+1=265.2). 100921 Example 4. Preparation of tert-butyl 4-((Z)-I-cyano-2 phenylisoureido)phenylcarbamate (4) H ON Y,~ -C 0 O N N O H 4 10093] To a suspension of diphenyl cyanocarbonimidate (11.04 g, 46.4 mmol) in 130 ml isopropanol was added Iert-butyl 4-aminophenylcarbamate (9.20 g, 44.2 mmol). The reaction was stirred at room temperature overnight and the solid was collected by filtration. Solid was dried under vacuum and it was weighted at 10.85g (69.7% yield). LC/MS (M+1=353.2). 116 [00941 Example 5. Preparation of 5

H

2 N N N N N HN N N rO H N NHBoc 5 [00951 To a solution of 3 (3.17 g, 12.0 mmol) and tert-butyl 4-((Z)-1-cyano-2 phenylisoureido)phenylcarbamate (4, 3.52 g, 10.0 mmol) in 6 ml NMP was added 1 ml DIEA. The reaction was sealed in a microwave reaction tube and heated in a microwave reactor at 180 degree over 6 min. The reaction was cooled to room temperature and partitioned between ethyl acetate and water. The organic layer was washed with water twice and was dried over Na2SO4. Removol of solvent left yellow solid. This solid was washed by DCM to afford a white solid. NMR: DMSO-d6: 8.98 (bs, I H); 8.94 (s, I H); 8.38 (s, 1 H); 7.72 (bs, 2H); 7.45 (d, 2H); 7.25 (d, 2H); 6.73 (s, 1 H); 4.60-4.10 (m, 4H); 3.20 (m, 2H); 2.02 (s, 3H); 1.40 (s, 9H); 1.15 (m, 6H). LC/MS (M+1=523.3). [00961 Example 6. Preparation of 1-((2S,6R)-4-(6-(3-(4-aminophenylamino)-5-amino- 1 H 1,2,4-triazol- I -yl)pyrimidin-4-yl)-2,6-dimethylpiperazin- 1 -yl)ethanone (6)

H

2 N N N NN ) N N N HN N rO H N

NH

2 6 100971 To a solution of 6 (2.0 g, 3.83 mmol) in 15 ml DCM was added 5 ml TFA. The reaction was stirred at room temperature over 30min. HPLC showed the completion of the reaction. The solvent was removed in vacuum and the resulting oily material was partitioned between DCM and aqueous NaHCO 3 . The organic layer was washed by aqueous NaHCO 3 several times and was dried over Na 2

SO

4 . Removal of solvent afforded 1.56 g desired product (the yield is 96.9%). 117 [00981 Example 7. General method for formation of carbamate. Following is a typical example for the formation of carbamate. Preparation of 1-76

H

2 N N N N / N )A N H ; N N 0 H N 0 1-76 100991 To a solution of 1-((2S,6R)-4-(6-(3-(4-aminophenylamino)-5-amino- I H- 1,2,4 triazol-1-yl)pyrimidin-4-yl)-2,6-dimethylpiperazin-1-yl)ethanone (21 mg, 0.05 mmol) in 2 ml DMF was added ethyl chloroformate (6.5 mg, 0.06 mmol, 1.2 equiv.). A drop of DIEA was also added to the reaction. The reaction was stirred at room temperature over 20min. The reaction crude was injected onto P-HPLC and 18 mg of desired product was obtained as a TFA salt. [001001 Example 8. General method for formation of a urea. 1001011 The following is a typical example for the formation of a urea:

H

2 N N'N NN N N rO H N - 0 NN H 1-67 [001021 To a solution of l-((2S,6R)-4-(6-(3-(4-aminophenylamino)-5-amino- I H-1,2,4 triazol-1-yl)pyrimidin-4-yl)-2,6-dimethylpiperazin-1-yl)ethanone (21 mg, 0.05 mmol) in 2 ml DMF was added isocyanatoethane (4.2 mg, 0.06 mmol, 1.2 equiv.). A drop of DIEA was also added to the reaction. The reaction was stirred at room temperature over 20min. The reaction crude was injected onto P-HPLC and 17 mg of desired product was obtained as a TFA salt. 118 1001031 Example 9. Preparation of 9

H

2 N N N N N N H N N N Boc 9 1001041 To a solution of 3 (1.58 g, 12.0 mmol) and tert-butyl 4-(4-((Z)-1-cyano-2 phenylisoureido)phenyl)piperazine-1-carboxylate (2.10g, 5.0 mmol) in 6 ml NMP was added 1 ml DIEA. The reaction was sealed in a microwave reaction tube and heated in a microwave reactor at 180 degree over 6 min. The reaction was cooled to room temperature and partitioned between ethyl acetate and water. The organic layer was washed with water twice and was dried over Na2SO4. Removol of solvent left yellow solid. This solid was washed by DCM to afford a white solid. NMR in DMSO-d6: 8.86 (s, 1 H); 8.38 (s, I H); 7.70 (bs, 2H); 7.48 (d, 2H); 6.90 (d, 2H); 6.70 (s, I H); 4.65-4.15 (m, 4H); 3.45 (m, 4H); 3.18 (m, 2H); 2.98 (m, 4H); 2.20 (s, 3h); 1.38 (s, 9H); 1.22 (m, 6H); LC/MS (M+1=592.3). 1001051 Example 10. Preparation of 1-((2S,6R)-4-(6-(3-(4-(piperazin- 1 -yl)phenylamino)-5 amino-I H- 1,2,4-triazol- I -yl)pyrimidin-4-yl)-2,6-dimethylpiperazin- 1 -yl)ethanone (10)

H

2 N N N H/ N NkAO N H N N N H 10 [001061 To a solution of 9 (1.0 g, 1.70 mmol) in 15 ml DCM was added 5 ml TFA. The reaction was stirred at room temperature over 30min. HPLC showed the completion of the reaction. The solvent was removed in vacuum and the resulting oily material was partitioned between DCM and aqueous NaHCO3. The organic layer was washed by aqueous NaHCO3 several times and was dried over Na2SO4. Removal of solvent afforded 805 mg desired product (the yield is 96.9%). 119 1001071 Example 11. Preparation of 1-113

H

2 N N N NN N N N r H N 0O N N 0 I-113 [00108] The general method for formation of carbamate as described above was utilized here to prepare I- 113. [001091 Example 12. Preparation of 1-60

H

2 N N N H /- N N O N HN N NH 0 1-60 1001101 The general method for formation of urea as described above was utilized here to prepare 1-60. 120 1001111 Scheme 4: Route to diamino triazole compounds

H

2 N "zNH 2 NN NH N CI H N N N aN bN N rO Nl a b HN Ci HN HN

NH

2 HN HN

H

2 N

H

2 N N METHOD N N N ) Nr0 A ): NNr H N -OHN NO METHOD O

NH

2 METHOD B HN-O

H

2 N N H2N N N N N I N N N N ON 0 HN HN - 0 - 0 HN-\ H N- N H [001121 (a) N-cyano-N'-(4-acetamidophenyl)-O-phenylisourea, NMP, DIEA, MW, 220 'C; (b) i: cis-2,6-dimethylpierazine, NMP, MW, 250 'C, ii: Ac 2 0, base; (c) 6N HCI, 95 *C; METHOD A: isopropyl chloroformate, DIEA, DMF; METHOD B: isopropyl isocyanate, DIEA, DMF; METHOD C: isovaleric acid, DCC, DCM. 1001131 Scheme 5: Route to diamino triazole compounds. HN CN HNN CN H N CIH N N 0 a j:N b N N O HN HN - HN N N N N N N 0 0 0 121 1001141 1-(2-chloropyridin-4-yl)-hydrazine, NMP, MW, 220 'C; (b) cis-2,6 dimethylpiperazine, NMP, MW, 250 'C. 1001151 Example 13.

H

2 N CI HN CI HN

NH

2 HN# N-{4-[5-Amino-1-(2-chloro-pyridin-4-yl)-1H-11,2,4]triazol-3-ylamino]-phenyl)-acetamide. A microwave reaction vessel was charged with 1.34 g of (2-Chloro-pyridin-4-yl)-hydrazine (7.48 mmol, 1.1 equiv) and 2.00 g of N-cyano-N'-(4-acetamidophenyl)-O-phenylisourea (6.80 mMol, I equiv). The solids were dissolved in 40 mL of NMP and 8 mL of DIEA. The sealed vessel was warmed to 220 *C for 6 min via microwave irradiation. Upon cooling, the resulting solution was poured into 200 mL of saturated sodium bicarbonate. The precipitate was collected and washed with 3 x 100 mL of water. After azeotropic drying (3 x 50 mL of acetonitrile) the dark yellow solid (2.0 g, 5.80 mMol, 85% yield) was used without further purification. 1H NMR (500 Mhz, DMSO-d 6 ) 8 9.68 (1 H, s), 9.00 (1 H, s), 8.40 (1 H, d), 7.67 (2 H, m), 7.50 (2 H, d), 7.40 (2 H, d), 6.95 (2 H, s), 2.0 (3 H, s) ppm. LCMS: 2.16 minutes/ 343.95 (M+H). 1001161 Example 14. Preparation of 1-35 H2NCI N N N NN 0 N N N rO HN ' HN - 0 - 0 HN HN 1-35 N-(4- {1-[2-(4-Acetyl-3,5-dimethyl-piperazin-1 -yl)-pyridin-4-yl ]-5-amino-1H- 11,2,4] triazol 3-ylamino}-phenyl)-acetamide. To a solution of 100 mg of N-{4-[5-Amino-1-(2-chloro pyridin-4-yl)-IH-[1,2,4]triazol-3-ylamino]-phenyl}-acetamide (0.291 mMol, I equiv) in 5 mL of NMP was added 100 mg of cis-2,6-dimethylpiperazine (0.877 mMol, 3.0 equiv). The stirred solution was heated to 250 'C via microwave irradiation for 15 min. The reaction mixture was 122 concentrated under vacuum by pouring and then redissolved in 5 mL of CH 2 Cl 2 and 5 mL of DMF. To the stirred solution was added sequentially I mL of Hunig's base and 100 PL of acetic anhydridide. After 3 hr at 25 'C, the reaction mixture was concentrated to a dark oil and purifed by flash chromatography (EtOAc), yielding 15 mg of N-(4-{l-[2-(4-Acetyl-3,5 dimethyl-piperazin- I -yl)-pyridin-4-yl]-5-amino-I H-[ 1,2,4]triazol-3-ylamino}-phenyl) acetamide (0.0323 mMol, 1 I % yield) as a yellow solid. Example 15. Preparation of 1-41

H

2 N N

H

2 N N' N N N' N N H N N O HN NO HN-k

NH

2 1-35 A 1001171 Compound A: 223.4 mg (0.48 mmol) of 1-7 was dissolved in 2.0 ml of 6N HCl. The reaction mixture was heated to 95 degrees. After 1 hour, the reaction mixture was allowed to cool to RT. All volatiles were removed at reduced pressure. The last trace of water was azeotropically removed by co-distillation with toluene. The residue was pumped down with hi vac overnight. Yield: Assume 100%. 'H NMR (500 MHz, DMSO-d 6 ) a 8.36 (s, br, 1H), 8.11 (s, br, I H), 7.25 (s, br, 2H), 6.90 (d, br, 2H), 6.53 (d, br, 4H), 4.59 - 3.98 (m, 6H), 3.04 (s, br, 2H), 2.03 (m, 3H), 1.20 S, br, 6H). LC/MS: 1.51 min/422.2 (M+H). [001181 Example 16. Preparation of 1-103

H

2 N N H 2 N N N N N METHOD N N N O A H N N O H N H N N

-

0

NH

2 HN O A 1-103 1001191 METHOD A: 1-103: 46.0 mg (0.10 mmol) of 1-7, 80 d (0.46 mmol) of DIEA and 120 pl of a 1.0 M solution of isopropyl chloroformate (0.12 mmol) were dissolved in 1.0 ml of DMF. The reaction mixture was allowed to stir at RT overnight. The reaction mixture was diluted with 2.0 ml of H 2 0 and filtered through a 0.45 im disc. The resulting solution was then 123 injected on to the preparative HPLC system (in 2 batches) and eluted with 5-95% Acetonitrile /Water. Yield: 8.8 mg, approximately 14%. 1001201 Example 17. Preparation of 1-107

H

2 N H 2 N NN N METHOD N NN HN:: N N O B H N N O H N - HN O

NH

2 HN N H A 1-107 [00121] METHOD B: 1-107: 55.0 mg (0.12 mmol) of 1-7, 100 d (0.56 mmol) of DIEA and 12.3 mg (0.14 mmol) of Isopropyl isocyanate were dissolved in 1.0 ml of DMF. The reaction mixture was allowed to stir at RT overnight. The reaction mixture was diluted with 2.0 ml of

H

2 0 and filtered through a 0.45 ptm disc. The resulting solution was then injected on to the preparative HPLC system (in 2 batches) and eluted with 5% -95% Acetonitrile / Water. Yield: 35.3 mg, approximately 47 %. [001221 Example 18. Preparation of I-111

H

2 N -N

H

2 N N N N N METHOD N N N HN N HN N N O

-

0

NH

2 HN A I-1ll 1001231 METHOD C: 1-111: 31.2 mg (0.30 mmol) of Isovaleric acid was dissolved in 850 ptl of CH2CI2. Added was 150 pl (0.15 mmol) of a 1.0 M solution of DCC in CH2CI2. After stirring for 15 min. at RT, the solution was filtered onto 55.6 mg (0.121 mmol) of 1-7. The filtered material was washed through with 2.0 ml of DMF. The resulting reaction mixture was allowed to stir at RT overnight. The reaction mixture was diluted with 2.0 ml of H 2 0 and filtered through a 0.45 ptm disc. The resulting solution was then injected on to the preparative HPLC system (in 2 batches) and eluted with 10% -90% Acetonitrile / Water. Yield: 23.6 mg, approximately 40 %. 124 [001241 Example 19. Preparation of I-111 CNHN C HN -i HN N N N HN 0 0 (7) (8) (8): 5.25 g (13.3 mmol) of (7), 3.78 g (17.5 mmol) of (2-Chloro-pyridin-4-yl)-hydrazine and 13.3 ml (74.7 mmol) of DIEA were suspended in 26.6 ml of NMP. The reaction mixture was capped and heated to 220 degrees C via microwave irradiation. After 6 min., the reaction mixture was allowed to cool to RT. The reaction mixture was then poured onto a saturated aqueous solution of sodium bicarbonate. This aqueous phase was diluted with EtOAc and the layers were separated. The organic was dried over MgSO4, filtered and evaporated to dryness. This crude material was chromatographed on 6 inches of silica gel and eluted with 5 - 9 % MeOH / CH2Cl2. The still slightly crude material was recrystallized from EtOAc / Hexane. Yield: 1.38 g, approximately 23%. [00125] Example 20. Preparation of 1-113

H

2 N r- HN r H N CI H N N N N H N H N N N 0 0 9 1-113 1001261 1-55: 603.6 mg (1.36 mmol) of (9) and 622.5 mg (5.5 mmol) of 2,6-Dimethyl piperazine were suspended in NMP. The reaction mixture was warmed to 250 degrees via 125 microwave irradiation. After 15 min., the reaction mixture was allowed to cool to RT. Added was 130 pl (1.6 mmol) of pyridine followed by 1.3 ml (13.8 mmol) of Acetic Anhydride. After 30 min., the reaction mixture was slowly added to a saturated solution of sodium bicarbonate. The product was extracted with EtOAc, dried over MgSO4, filtered and evaporated to dryness. This crude material was chromatographed on 6 inches of silica gel and eluted with 5 - 9 % MeOH / CH 2

CI

2 . Yield: 108 mg, approximately 14%. [001271 Example 21. NMR and Mass Spectrometry of Compounds 1001281 Analytical data for certain compounds of the present invention was collected and recorded as follows: Proton NMR was collected using a Bruker AMX 500 instrument and appropriate solvent. The LC/MS method used a Hypersil BDS C18 5 micron 2.1 x 50 mm column with a flow rate of 1.Oml/min with an appropriate gradient. Mass spectrometer samples were analyzed on a MicroMass ZQ or Quattro II mass spectrometer operated in single MS mode with electrospray ionization. Samples were introduced into the mass spectrometer using flow injection (FIA) or chromatography. Mobile phase for all mass spectrometer analysis consisted of acetonitrile-water mixtures. TFA in some instances. Table 2 below depicts exemplary LC mass spectral data (LC/MS), retention time (RT) and 'H-NMR data for certain compounds of the present invention, wherein compound numbers in Table 2 correspond to the compounds depicted in Table I (empty cells indicate that the test was not performed). Table 2 Cmpd # LC/MS RT NMR 2.11 500MHzCH3CN-d3: 8.05(m,IH), 7.75(d,2H), 7.6(d,2H), 7.2(m,2H), 3.9(m,7H), 3.7(m,6H), 2.15(s,3H) 2.0(m,5H) I H NMR (500 MHz, DMSO-d6) d 8.95 (I H, br s), 8.39 (I H, d), 7.73 2 479.00 1.96 2 H, br s), 7.51 (2 H, d), 6.99 (2 H, br s), 6.61 (I H, d), 3.88 (7 H, i), 3.63 (5 H, m), 3.44 (2 H, t), 3.40 (2 H, t), 1.95-1.93 (3 H, m), 1.82 (2 H, m) ppm. I H NMR (500 MHz, DMSO-d6) d 8.86 (1 H, s), 8.40 (1 H, s), 7.73 (2 3 451.00 1.76 H, s), 7.69 (1 H, t), 7.50 (2 H, d), 6.89 (2 H, d), 6.80 (1 H, s), 4.30 (2 H, t), 3.83 (2 H, m), 3.71 (5 H, m), 3.42 (4 H, m), 3.30 (3 H, m), 3.0 (4 H, m), 2.60 (2 H, m) ppm. 1 H NMR (500 MHz, DMSO-d6) d 9.05 (1 H, br s), 8.40 (I H, d), 7.78 4 534.00 1.96 (2 H, br s), 7.56 (2 H, br s), 7.40-6.90 (3 H, m), 6.63 (1 H, br s), 3.98 2.47 3.60 (8 H, m), 3.54 (I H, m), 3.40 (2 H, m), 3.42 (4 H, m), 3.0 (4 H, m) PPm. 5 2.44 6 2.43 7 2.48 8 2.59, 2.61 9 2.65 DMSO-d6: 9.42 (bs, I ho; 8,32 (d, 1 H); 7.81 (bs, 2H); 7.68 (d, 2H); 7.49 10 437.20 1.50 (m, 2h); 6.65 (d, I H); 3.60-4.00 (m, 6H); 3.42 (m, 2H); 3.08 (m, 6H); 1.75-1.98 (m, 5H); 126 Cmpd # LC/MS RT NMR DMSO-d6: 9.6 (s, 1 H); 9.03 (s, I H); 8.35 (d, I H); 7.80 (bs, 2H); 7.45 (d, II 451.10 2.20 2H); 7.42 (d, 2H); 6.62 (m, I H); 4.55 (m, I H); 3.55-3.95 (m, 6H); 3.43 (m, 2H); 1.75-1.95 (m, 5H); 1.95 (s, 3H)l.30 (dd, 6H) DMSO-d6: 10.90 (bs, 0.9H); 9.55 (s, I H); 8.36 (d, I H); 7.82 (bs, 2H); 12 465.10 1.70 7.75 (d, 2H); 7.50 (m, 21H); 6.63 (in, I H); 3.40-3.95 (m, 12H); 1.75-1.98 (m, 5H); 1.02 (t, 6H) DMSO-d6: 9.52 (s, I H); 8.41 (d, I H); 7.81 (bs, 2H); 7.75(m, 2H); 7.51 13 477.00 1.80 (m, 2H); 6.65 (m, I H); 3.40-3.95 (m, 6H); 3.45 (m, 6H); 1.40-1.98 (m, I IH); 500 MHz (dmso) 9.00 (s, I H), 8.05 (d, 1 H), 7.49 (d, I H), 7.18 (m, 2H), 14 437.00 2.10 7.17-6.95 (complex m, 4H), 3.76 (complex m, 6H), 3.76 (m, 4H), 3.69 (dd, 2H), 1.94 (m, 2H) ppm 15 2.72 50OMHz,DMSO-d6: 9.l(br m,IH), 8.4(s,IH), 7.77(m,2H), 16 2.60 7.6(m,2H), 7.l(m,2H), 6.77(s,IH),4.3(m,3H), 3.8(m,4H), 3.2(m,7H), 2.03(s,3H), 1.15(br m,6H) 500 Hz (dmso) 8.98 (s, I H), 8.11 (d, I H), 7.51 (d, 2 H), 7.16-6.97 (m, 17 492.00 2.50 4H), 6.91 (m, 2H), 4.70-4.17 (broad m, 2H), 4.15 (d, 2H), 3.78 (m, 4H), 3.24 (m, 2H), 3.13 (m, 4H), 2.03 (s, 31H), 1.23 (m, 6H) ppm 500 Hz (dmso) 8.92 (s, I H), 8.03 (d, I H), 7.47 (d, 2H), 7.20-6.93 (br m, 18 461.00 2.90 4H), 6.91 (m, 2H), 3.75 (m, 8H), 3.03 (m, 4H), 2.21 (m, 2H), 1.68 (s, 8H) ppm 500 Hz (dmso) 9.00 (s, I H), 8.00 (d, I H), 7.48 (d, 2H), 7.18 (m, I H), 19 435.00 2.70 7.07 (br s, 2H), 7.03 (s, I H), 6.93 (d, 2H), 3.75 (dd, 4H), 3.71 (dd, 4H), 3.05 (m, 4H), 1.81 (m, 4H), 1.55 (im, 4H) ppm DMSO-d6: 9.70 (bs, 2H); 9.35 (bs, I H); 8.35 (d, I h); 7.80 (bs, 2h); 7.68 20 409.00 2.20 (d, 2H); 7.22 (d, 2H); 6.62 (m, I H); 3.62-3.98 (m, 61H); 3.35-3.45 (m, 2H); 1.75-1.98 (m, 5H) DMSO-d6: 9.02 (bs, I H); 8.98 (s, I H); 8.35 (d, I H); 7.76 (bs, 2 H); 7.45 21 509.00 3.10 (d, 2H); 7.28 (d, 2H); 6.62 (m, 1 H); 3.55-4.00 (m, 6H _; 3.42-3.50 (m, 2H); 1.72-1.98 (m, 5H); 1.42 (s, 9H) 500 MHz (dmso) 9.08 (br s, I H), 8.42 (s, I H), 7.78 (br s, 2H), 7.58 (d, 22 477.00 3.30 2H), 7.12 (br s, 2H), 6.81 (s, I H), 4.62 (n, I H), 4.43 (m, I H), 3.92 (d, I H), 3.81 (m, 4H), 3.60 (m, I H), 3.20 (m, 4 H), 2.94 (ddd, I H), 2.84 (ddd, I H), 2.76 (t, I H), 2.30 (m, 2 H), 2.18 (m, I H), 1.65 (m, I H) 23 477.00 3.20 24 533.00 3.30 DMSO-d6: 9.52 (s, I H); 9.02 (s, I H); 8.35 (d, I H); 7.74 (bs, 2H); 7.48 25 561.10 3.80 (m, 4H); 6.60 m, I H); 3.55-4.00 (m, 6 H); 3.45 (m, 2 H); 2.15 (i, I H); 1.75-1.95 (m, 9H); 1.15-1.45 (m, 7H); 0.85-0.95 (m, 5H); DMSO-d6: 9.62 (s, I H); 9.02 (s, I H); 8.35 (d, I H); 7.74 (bs, 2H); 7.48 26 521.00 2.40 (m, 4H); 6.62 (m, I H); 3.55-4.00 (n, 8 H ); 3.45 (m, 4H); 2.45 (m, I H); 1.75-1.95 (m, 5H); 1.60 (m, 4H) DMSO-d6: 10.28 (s, I H); 9.18 (s, I H); 9.15 (s, I H); 8.76 (d, I H); 8.35 27 514.00 2.10 (d, 2H); 7.78 (bs, 2H); 7.54-7.60 (m, 5H); 6.62 (m, I H); 3.55-4.00 (m, 6H); 3.40-3.45 (m, 2H); 1.75-1.98 (n, 5H) DMSO-d6: 10.40 (s, I H); 9.18 (s, I H); 8.80 (d, 2H); 8.40 (d, I H); 7.90 28 514.00 2.10 (d, 2H); 7.78 (bs, 2H); 7.54-7.60 (m, 4H); 6.62 (in, I H); 3.55-4.00 (m, 6H); 3.40-3.45 (m, 2H); 1.75-1.98 (m, 5H) DMSO-d6: 9.73 (s, I H); 9.18 (s, 1 H); 8.42 (d, I H); 8.34 (s, I H); 9.78 (s, 29 503.00 2.60 I H); 9.77 (bs, 2H); 7.55 (m, 4H0; 6.95 (s, I H); 6.63 (m, I H); 3.55-4.00 (m, 6H); 3.40-3.45 (m, 2H); 1.75-1.98 (m, 5H) DMSO-d6: 9.95 (s, I H); 9.13 (s, I H); 8.34 (d, I H); 7.92 (s, I H); 7.78 30 503.00 2.60 (bs, 2H); 7.55 (m, 4H); 7.26 (d, I H); 6.65 (m, 2H); 3.55-4.00 (m, 6H); 3.40-3.45 (m, 2H); 1.75-1.98 (m, 5H) 31 549.00 2.70 32 549.00 2.75 127 Cmpd # LC/MS RT NMR DMSO-d6: 9.02 (bs, I H); 8.40 (d, I H); 7.75 (bs, 2H); 7.50 (m, 2H); 7.03 33 507.10 2.30 (m, 2H); 6.60 (m, I H); 3.60-4.00 (m, 8H); 3.45 (m, 4H); 2.45 (m, 2H); 1.75-2.00 (m, 5H); 1.15 (d, 6H) DMSO-d6: 8.88 (s, I H); 8.35 (d, I H); 7.65 (bs, 2H); 7.48 (d, 2H); 6.85 d, 2H); 6.62 (m, I HO; 3.40-4.00 (m, 12H); 2.94 (m, 4H); 1.75-2.00 (m, 578.10 2.80 5H); 1.40 (s, 9H) 578.20 2.70 DMSO-d6: 08.85 (s, I H); 8.31 (d, I H); 7.69 (s, 2H); 7.45 (d, 2H); 6.85 34 578.30 2.70 (d, 2H); 6.62 (m, I H); 4.00-3.55 (m, 6H); 3.40 (m, 6H); 2.92 (m, 4H); 578.40 2 70 2.00-1.75 (m, 5H); 1.32 (s, 9H) DMSO-d6: 9.25 (bs, I H); 8.35 (d, I H); 7.80 (bs, 2H); 7.62 (m, 2H); 7.22 m, 2 H); 6.62 (m, I H); 4.00-3.55 (m, 10 H); 3.50 (m, 2 H); 3.28 (m, 4 H); 2.32 (m, 3H); 2.00-1.75 (m, 5H); 1.35 (s, 9H) I H NMR (500 MHz, MeOD-d4) d 8.14 (I H, d), 7.48 (2 H, d), 7.40 (3 35 464.08 1.63 H, m), 7.03 (1 H, s), 6.95 (1 H, d), 3.70 (2 H, m), 3.30 (4 H, m), 2.15 (3 H, s), 2.09 (3 H, s), 1.30 (6 H, d) ppm. DMSO-d6: 9.02 (bs, I H); 8.38 (d, I H); 7.73 (bs, 2H); 7.50 (m, 2H); 7.03 36 562.10 2.50 'm, 2h); 6.60 (m, I H); 3.30-4.00 (m, 12H); 3.08 (m, 4H); 1.75-2.00 (m, 5 H); 1. 19 (s, 9H) DMSO-d6: 9.02 (bs, I H); 8.38 (d, I H); 7.73 (bs, 2H); 7.52 (m, 2H); 7.03 37 548.10 2.30 (m, 2H); 6.62 (m, 1H); 3.30-4.00 (m, 12H); 3.08 (m, 4H); 2.32 (t, 2H); 1.75-2.00 (m, 5H); 1.58 (m, 2H); 0.85 (t, 3H) DMSO-d6: 9.02 (bs, I H); 8.38 (d, I H); 7.73 (bs, 2H); 7.52 (m, 2H); 7.03 38 562.20 2.50 'm, 2H); 6.62 (m, I H); 3.30-4.00 (m, 12H); 3.08 (m, 4H); 2.22 (d, 2H); 1.75-2.00 (m, 6H); 0.88 (d, 6H) DMSO-d6: 9.02 (bs, I H); 8.38 (d, I H); 7.73 (bs, 2H); 7.52 (m, 2H); 7.03 39 546.10 2.20 (m, 2H); 6.62 (m, I H); 3.30-4.00 (m, 12H); 3.08 (m, 4H); 1.75-2.00 (m, 6H); 0.72 (m, 4H) DMSO-d6: 9.02 (bs, I H); 8.38 (d, I H); 7.73 (bs, 2H); 7.52 (m, 2H); 7.03 40 560.10 2.40 (m, 2H); 6.62 (m, I H); 3.30-4.00 (m, I 2H); 3.08 (m, 4H); 2.10-2.20 (m, 4H); 1.75-2.00 (m, 8H) DMSO-d6: 9.02 (bs, I H); 8.38 (d, I H); 7.73 (bs, 2H); 7.52 (m, 2H); 7.03 41 590.10 2.20 (m, 2H); 6.62 (m, I H); 3.50-4.00 (m, 12H); 3.37-4.43 (m, 4H); 3.08 (m, 4H); 2.90 (m, I H); 1.75-2.00 (m, 5H); 1.60 (m, 4H) 42 478.10 1.60 DMSO-d6: 9.02 (bs, I H); 8.40 (d, I H); 7.75 (bs, 2H); 7.50 (m, 2H); 7.00 43 592.20 2.20 (m, 2H); 6.60 (m, I H); 5.18 (m, I H); 3.40-4.00 (m, 1 6H); 3.15 (m, 4H); 1.75-2.00 (m, 7H) DMSO-d6: 9.02 (bs, I H); 8.40 (d, 1 H); 7.75 (bs, 2H); 7.50 (n, 2H); 7.05 44 548.20 2.30 (m, 2H); 6.60 (m, I H); 3.40-4.00 (m, I 2H); 3.15 (m, 4H); 2.95 (m, I H); 1.75-2.00 (m, 5H); 1.02 (d, 6H) DMSO-d6: 9.10 (bs, I H); 8.38 (d, I H); 7.75 (bs, 2H); 7.60 (m, 2H); 7.05 45 536.10 2.20 (m, 2H); 6.60 (m, I H); 3.40-4.00 (m, 15 H); 3.15 (m, 4H);1.75-2.00 (m, 5H); DMSO-d6: 9.10 (bs, I H); 8.38 (d, I H); 7.75 (bs, 2H); 7.60 (m, 2H); 7.05 46 550.10 2.40 (m, 2H); 6.60 (m, I H); 4.08 (q, 2H); 3.40-4.00 (i, 12H); 3.15 (m, 4H);1.75-2.00 (m, 5H); 1.15 (t, 3H) DMSO-d6: 9.10 (bs, I H); 8.38 (d, I H); 7.75 (bs, 2H); 7.60 (m, 2H); 7.05 (m, 2H); 6.60 (m, I H); 4.03 (q, 2H); 3.40-4.00 (m, 12H); 3.15 (m, 4H);1.75-2.00 (m, 5H); 1.55 (m, 2H); 0.88 (t, 3H) 564.20,56 2.702.60 DMSO-d6: 8.88 (s, I H); 8.38 (d, I H); 7.68 (bs, 2H); 7.46 (d, 2H); 6.88 47 4.50,564.4 2.60 (d, 2H); 6.60 (m, I H); 3.95 (t, 2H); 4.00-3.55 (m, 6H); 3.50-3.38 (m, 0 6H); 2.98 (m, 4H); 2.00-1.75 (m, 5H); 1.60 (m, 2H); 0.85 (t, 3H) DMSO-d6: 9.30 (bs, I H); 8.35 (d, I H); 7.76 )bs, 2H); 7.60 (m, 2H); 7.28 (m, 2H); 6.60 (m, I H); 3.98 (q, 2H); 4.00-3.55 (m, 8H); 3.40-3.20 (m, 8H); 2.30 (s, 3H); 1.95-1.75 (m, 5H); 1.55 (m, 2H); 0.88 (t, 3H) DMSO-d6: 9.10 (bs, I H); 8.38 (d, I H); 7.75 (bs, 2H); 7.60 (m, 2 H); 7.05 48 564.20 2.60 (m, 2H); 6.60 (m, I H); 4.80 (m, I H); 3.40-4.00 (m, 12H); 3.15 (m, 4H);1.75-2.00 (m, 5H); 1.22 (d, 6H) 128 Cmpd# LC/MS RT NMR DMSO-d6: 9.10 (bs, I H); 8.38 (d, I H); 7.75 (bs, 2H); 7.60 (m, 2H); 7.05 49 592.20 3.10 (m, 2H); 6.60 (in, I H); 3.40-4.00 (in, 14H); 3.15 (m, 4H); 1.75-2.00 (m, 5H); 0.90 (s, 9H) DMSO-d6: 9.10 (bs, I H); 8.38 (d, I H); 7.75 (bs, 2H); 7.60 (m, 2H); 7.05 50 578.20 3.10 (m, 2H); 6.60 (m, I H); 3.40-4.00 (m, 14H); 3.15 (m, 4H); 1.75-2.00 (in, 6H); 0.88 (d, 6H) DMSO-d6: 9.10 (bs, I H); 8.38 (d, I H); 7.75 (bs, 2H); 7.60 (m, 2H); 7,15 51 612.20 3.20 (d, 2H); 7.05 (m, 4H); 6.60 (in, I H); 3.40-4.00 (in, 12H); 3.15 (in, 4H); 2.22 (s, 3H); 1.75-2.00 (m, 6H); DMSO-d6: 8.86 (s, I H); 8.38 (s, I H); 7.70 (bs, 2H); 7.48 (d, 2H); 6.90 (d, 2H); 6.70 (s, 1 H); 4.65-4.15 (in, 4H); 3.45 (m, 4H); 3.18 (in, 2H); 52 592.30,59 3.00,2.90 2.98 (m, 4H); 2.20 (s, 3h); 1.38 (s, 9H); 1.22 (in, 6H) 2.40 DMSO-d6: 9.25 (bs, I H); 8.35 (s, I H); 7.78 (bs, 2H); 7.62 (d, 2H); 7.23 (m, 2H); 6.75 (s, I H); 4.60-4.00 (m, 6H); 3.22 (in, 8H); 2.28 (s, 3H); 2.02 (s, 3 H); 1.41 (s, 9H); 1.18 (m, 6H) DMSO-d6: 9.12 (bs, 1 H); 8.35 (s, 1 H); 7.75 (bs, 2H); 7.56 (m, 2H); 7.10 53 550.30 2.40 (m, 2H); 6.76 (m, I H); 4.65-4. 10 (in, 4H); 3.38 (s, 3h); 3.50 (in, 4h); 3.15 (m, 6H); 2.20 (s, 3 H); 1.12 (in, 6H) DMSO-d6: 9.09 (bs, I H); 8.39 (s, I H); 7.80 (bs, 2H); 7.56 (m, 2H); 7.08 (m, 2H); 6.76 (m, I H); 4.65-4.10 (m, 4H); 4.03 (q, 2H); 3.50 (in, 4H); 54 564.30,56 2.60,2.60 3.20-3.10 (m, 6H); 2.10 (s, 3H); 1.15 (t, 3H); 1.12 (m, 6H) 4.30 DMSO-d6: 9.22 (bs, I H); 8.38 (s, I H); 7.78 (bs, 2H); 7.60 (m, 2H); 7.20 (m, 2H); 6.65 (s, 1 H); 4.60-4.00 (in, 4H); 4.06 (q, 2H); 3.80 (in, 4H); 3.20 (m, 6H); 2.32 (s, 3H); 2.02 (s, 3h); 1.18 (t, 3H); 1.15 (m, 6H) DMSO-d6: 9.09 (bs, I H); 8.35 (s, 1 H); 7.75 (bs, 2H); 7.56 (m, 2H); 7.08 (m, 2H); 6.76 (m, I H); 4.65-4. 10 (in, 4H); 4.00 (q, 2H); 3.55 (in, 4H); 3.30-3.10 (in, 6H); 2.10 (s, 3H); 1.15 (t, 3H); 1.55 (m, 2H); 1.12 (in, 5 578.40,57 2.80,2.80 6H); 0.85 (t, 3H) 8.40 DMSO-d6: 9.22 (bs, 1 H); 8.38 (s, I H); 7.78 (bs, 2H); 7.60 (in, 2H); 7.20 (m, 2H); 6.65 (s, 1 H); 4.60-4.00 (m, 4H); 4.00 (q, 2H); 3.80 (m, 4H); 3.20 (m, 6H); 2.32 (s, 3H); 2.02 (s, 3h); 1.58 (m, 2H); 1.15 (m, 6H); 0.88 (t, 3H) DMSO-d6: 9.08 (bs, 1-H); 8.38 (s, I H); 7.78 (bs, 2H); 7.56 (m, 2H); 7.05 56 578.40 2.80 (m, 2H); 6.75 (m, I H); 4.80 (in, I H); 4.60-4.10 (m, 4H); 3.52 (m, 4H); 3.25-3.05 (in, 6H); 2.02 (s, 3H); 1.22 (d, 6H); 1. 15 (m, 6H) ( DMSO-d6: 9.08 (bs, I H); 8.38 (s, I H); 7.78 (bs, 2H); 7.56 (m, 2H); 7.05 57 606.40 3.30 (in, 2H); 6.75 (in, I H); 4.60-4.10 (in, 4H); 3.70 (s, 2H); 3.52 (in, 4H); 3.25-3.05 (in, 6H); 2.02 (s, 3H); 1.22 (m, 6H);0.92 (s, 9H) DMSO-d6: 9.08 (bs, I H); 8.38 (s, I H); 7.78 (bs, 2H); 7.56 (in, 2H); 7.05 58 592.40 3.10 (m, 2H); 6.75 (m, I H); 4.60-4.10 (in, 41H1); 3.80 (d, 2H); 3.52 (m, 4H); 3.25-3.05 (m, 6H); 2.02 (s, 3 H); 1.85 (m, I H); 1.22 (in, 6H); 0.88 (d, 6H) DMSO-d6: 8.80 (s, I H); 8.38 (s, I I); 7.70 (bs, 2H); 7.48 (d, 2H); 6.85 59 492.40 1.80 (d, 2H); 6.78 (s, 1 H); 4.60-4.10 (in, 41-); 3.40-3.10 (m, 611); 2.95 (m, 2I); 2.85 (m, 2 H); 2.05 (s, 3 H); 1.12 (m, 6H) DMSO-d6: 9.18 (bs, I I); 8.32 (s, I H); 7.75 (bs, 2H); 7.60 (d, 2H); 7.20 60 563.40 2.20 (m, 2H); 6.76 (s, I H); 6.62 (bs, 1 H); 4.60-4.10 (in, 4 H); 3.50 (in, 4 H); 3.20 (in, 6H); 3.08 (q, 2 H); 2.06 (s, 3 H); 1.16 (m, 6 H); 0.98 (t, 3 H) DMSO-d6: 9.18 (bs, I I); 8.32 (s, I H); 7.75 (bs, 2H); 7.60 (d, 2H); 7.20 61 577.40 2.30 (in, 2H); 6.76 (s, I H); 6.62 (bs, I H); 4.60-4.10 (m, 4H); 3.55 (m, 4H); 3.22 (in, 6H); 3.00 (m, 2H); 2.06 (s, 3 H); 1.40 (in, 2H); 1. 16 (in, 6H); 0.80 (t, 3H) DMSO-d6: 9.22 (bs, 1 H); 8.38 (s, I H); 7.76 (bs, 2H); 7.62 (d, 2H); 7.22 62 577.40 2.30 (m, 2H); 6.76 (s, I H); 6.32 (m, I H); 4.60-4.10 (m, 4H); 3.72 (m, I H); 3.55 (in, 4H); 3.22 (in, 6H); 2.02 (s, 3H); l.18 (m, 6H); 1.02 (d, 6H) DMSO-d6: 9.22 (bs, I H); 8.38 (s, I H); 7.76 (bs, 2H); 7.62 (d, 2H); 7.22 63 591.40 2.50 (in, 2H); 6.76 (s, I H); 5.92 (m, I H); 4.60-4.10 (in, 4H); 3.55 (in, 4H); 3.22 (in, 6H); 2.02 (s, 3 H); l.22 (s, 9H); I.18 (m, 6H) 129 Cmpd # LC/MS RT NMR DMSO-d6: 9.22 (bs, I H); 8.38 (s, I H); 7.76 (bs, 2H); 7.62 (d, 2H); 7.22 64 617.40 2.60 (m, 2 H); 6.76 (s, I H); 5.92 (m, I H); 4.60-4.10 (m, 4H); 3.40-3.60 (m, 5H); 3.22 (m, 6H); 2.02 (s, 3H); 1.50-1.70 (m, 4H); 1.00-1.30 (m, 12H) DMSO-d6: 9.15 (bs, I H); 8.35 (s, I H); 7.76 (bs, 2H); 7.55 (d, 2H); 7.20 65 635.40 2.40 (m, 2 H); 6.76 (s, I H); 6.66 (m, I H); 4.60-4.10 (m, 4 H); 4.02 (q, 2 H); 3.50 (m, 4H); 3.25-3.05 (m, 8H); 2.50 (m, 2H)2.20 (s, 3H); 1.08 (m, 9H) DMSO-d6: 9.10 (s, I H); 8.35 (m, 2H); 7.75 (bs, 2H); 7.60 (m, 2H); 7.22 66 647.30 2.60 (m, I H); 7.10 (m, 2H); 6.85 (M, I H); 6.80 (s, I H); 6.50 (m, I H); 4.60 4.10 (m, 4 H); 3.60 (m, 4H); 3.18 (m, 6H); 2.05 (s, 3 H); 1.12 (m, 6H) DMSO-d6: 8.92 (s, I H); 8.35 (s, I h); 8.12 (s, I H); 7.75 (bs, 2H); 7.40 67 494.30 2.50 (d, 2H); 7.22 (d, 2H); 6.73 (s, I H); 5.90 (bs, I H); 4.60-4.10 (m, 4H); 3.20 (m, 2H); 3. 10 (q, 2H); 2.02 (s, 3H); 1.15 (bs, 6H); 1.02 (t, 3H) DMSO-d6: 8.92 (s, I H); 8.35 (s, I h); 8.12 (s, I H); 7.75 (bs, 2H); 7.40 68 508.30 2.70 (d, 2H); 7.22 (d, 2H); 6.73 (s, I H); 5.90 (bs, I H); 4.60-4.10 (m, 4H); 3.20 (m, 2H); 3.10 (q, 2H); 2.02 (s, 3H); 1.40 (m, 2H); 1.15 (bs, 6H); 1.02 (t, 3H) DMSO-d6: 8.92 (s, I H); 8.35 (s, I h); 8.12 (s, 1 H); 7.75 (bs, 2H); 7.40 69 508.30 2.70 (d, 2H); 7.22 (d, 2H); 6.73 (s, 1 H); 5.90 (bs, I H); 4.60-4.10 (m, 4H); 3.80 (m, I H); 3.19 (m, 2H); 2.02 (s, 3H); 1.15 (m, 6H); 1.05 (d, 6H) DMSO-d6: 8.92 (s, 1 H); 8.35 (s, I h); 8.12 (s, I H); 7.75 (bs, 2H); 7.40 70 522.30 2.90 (d, 2H); 7.22 (d, 2H); 6.73 (s, H); 5.90 (bs, 1 H); 4.60-4.10 (m, 4H); 3.19 (m, 2H); 2.02 (s, 3KH); 1.22 (s, 9H); 1.15 (m, 6H) DMSO-d6: 8.92 (s, I H); 8.35 (s, I h); 8.12 (s, H); 7.75 (bs, 2H); 7.40 71 548.40 3.10 (d, 2H); 7.22 (d, 2H); 6.73 (s, I H); 5.90 (bs, I H); 4.60-4.10 (m, 4H); 3.42 (m, I H); 3.20 (m, 2H); 2.02 (s, 3H); 1.78 (m, 2H); 1.68 (m, 2H); 1.55 (m, I H); 1.30-1.00 (m, I I H) DMSO-d6: 8.88 (s, I H); 8.30 (s, I h); 8.22 (s, I H); 7.75 (bs, 3H); 7.40 72 566.40 2.70 (d, 2H); 7.22 (d, 2H); 6.73 (s, H); 6.10 (bs, H); 4.60-4.10 (m, 4H); 4.03 (m, 2H); 3.32-3.15 (in, 4H); 3.02 (m, I H); 2.55 (m, I H); 2.02 (s, 3hO; 1.10 (m, 9H) DMSO-d6: 8.98 (s, IH); 8.60 (s, IH); 8.32 (s, 1H); 7.95 (s, lh); 7.75 (bs, 73 578.30 3.00 2H); 7.45 (d, 2h); 7.28 (d, 2H); 7.25 (m, I H); 7.08 (m, 1 H); 6.73 9s, I H); 4.60-4.10 (m, 4h); 3.15 9m, 2H); 2.02 (s, 3h0; 1.15 (m, 6H) DMSO-d6: 9.12 (s, I H); 9.02 (s, I H); 8.35 (s, I H); 7.85 (d, H); 7.92 (s, 74 610.30 3.40 1 H); 7.75 (bs, 2H); 7.60 (m, 2h); 7.48 (d, 2H); 7.28 (d, 2h); 7.20 (m, I H); 6.72 (s, I H); 4.60-4.10 (m, 4H); 3.20 (m, 2h); 2.02 (s, 3h); 1.15 (m, 6H) DMSO-d6: 9.22 (s, I H); 9.00 (s, 11-); 8.38 (s, I H); 7.70 (bs, 2H); 7.45 75 481.30 2.70 (d, 2 H); 7.30 (d, 2 H); 7.20 (m, I H); 6.72 (s, I H); 4.60-4.10 (m, 4 H); 3.60 (s, 3 H); 3.30 (m, 2 H); 1.12 (m, 6H) DMSO-d6: 9.22 (s, I H); 9.00 (s, I H); 8.38 (s, I H); 7.70 (bs, 2H); 7.45 (d, 2 I); 7.30 (d, 2 H); 7.20 (m, I H); 6.72 (s, I H); 4.60-4.10 (m, 4 H); 76 495.30 2.90 4.02 (q, 2 H); 3.20 (m, 2 H); 1.16 (t, 3 H); 1. 12 (m, 6HFI) 495.30 2.80 DMSO-d6: 9.30 (bs, I H); 9.02 (bs, I H); 8.40 (s, I H); 7.75 (bs, 2H); 7.50 (d, 2H); 7.35 (d, 2H); 6.75 (s, I H); 4.60-4.00 (m, 4H); 4.05 (q, 2H); 3.23 (m, 2 H); 2.25 (s, 3 H); 2.03 (s, 3 H); 1.22 (t, 3 H); 1.18 (m, 6H) ( DMSO-d6: 9.22 (s, 1 H); 9.00 (s, I H); 8.38 (s, 1 H); 7.70 (bs, 2H); 7.45 77 509.30 3.10 (d, 2H); 7.30 (d, 2H); 7.20 (m, I H); 6.72 (s, 1 H); 4.60-4.10 (m, 4H); 3.98 (t, 2H); 3.20 (m, 2H); 2.02 (s, 3H); 1.55 (m, 2H); 1. 15 (m, 6H); 10.89 (t, 3H) 509.30 3.10 DMSO-d6: 9.22 (s, I H); 9.02 (s, I H); 8.38 (s, 1 H); 7.78 (bs, 2H); 7.50 78 509.40 3.10 (d, 2H); 7.32 (d, 2H); 6.72 (s, I H); 4.84 (m, 1 H); 4.60-4.00 (m, 4H); 3.28 (m, 2 H); 2.02 (s, 3 H); 1.22 (d, 6H); 1.18 (m, 6H) 130 Cmpd # LC/MS RT NMR DMSO-d6: 9.23 (s, I H); 9.01 (s, I H); 8.38 (s, I H); 7.78 (bs, 2H); 7.48 (d, 2H); 7.32 (d, 2H); 6.78 (s, I H); 4.60-4.10 (m, 4H); 3.85 (d, 2H); 3.20 79 523.30 3.30 (m, 2H); 2.02 (s, 3H); 1.88 (in, I H); 1.15 (in, 6H); 0.86 (d, 6H),DMSO 523.30 3.30 d6: 9.22 (s, I H); 9.02 (s, I H); 8.38 (s, I H); 7.78 (bs, 2H); 7.50 (d, 2H); 7.32 (d, 2H); 6.72 (s, I H); 4.60-4.00 (in, 4H); 3.80 (d, 2H); 3.25 (in, 2H); 2.02 (s, 3H); 1.88 (in, I H); 1.18 (m, 6H); 0.98 (d, 6H) DMSO-d6: 9.23 (s, I H); 9.01 (s, I H); 8.38 (s, I H); 7.78 (bs, 2H); 7.48 (d, 2H); 7.32 (d, 2H); 6.78 (s, I H); 4.60-4.10 (in, 4H); 3.78 (d, 2H); 3.20 80 537.30 3.50 (in, 2H); 2.02 (s, 3H); 1.15 (in, 6H); 0.90 (s, 9H) 537.30 3.50 DMSO-d6: 9.22 (s, I H); 9.02 (s, I H); 8.38 (s, I H); 7.78 (bs, 2H); 7.50 (d, 2H); 7.32 (d, 2H); 6.72 (s, I H); 4.60-4.00 (m, 4H); 3.80 (s, 2H); 3.25 1(m, 2 H); 2.02 (s, 3 H); 1. 18 (in, 6H); 0.92 (s, 9H) DMSO-d6: 9.88 (s, I H); 9.03 (s, I H); 8.33 (s, I H); 7.74 (bs, 2h0; 7.53 (d, 2H); 7.32 (d, 2HO; 7.18 (d, 2h); 7.06 (d, 2HO; 6.72 (s, I H); 4.60-4.10 81 557.30 3.50 (in, 4 H); 3.16 (in, 2 H); 2.38 (s, 3 HO; 2.02 (s, 3 H); 1.15 (in, 6H) 557.30 3.50 DMSO-d6: 9.86 (bs, I H); 9.03 (s, I H); 8.35 (s, I H); 7.76 (bs, 2H); 7.55 (d, 2H); 7.35 (d, 2H); 7.21 (d, 2H); 7.05 (d, 2H); 6.75 (s, I H); 4.60-4.00 1(m, 4H); 3.22 (in, 2H); 2.30 (s, 3 H); 2.02 (s, 3H); 1.18 (m, 6H) DMSO-d6: 9.25 (s, I H); 8.95 (s, I H); 8.35 9s, I H); 7.72 (bs, 2H); 7.45 82 605.30 4.40 (d, 2H); 7.32 (d, 2H); 6.65 (s, I H); 4.60-4.10 (in, 6H); 3.20 (m, 2H); 2.05 (s, 3H); 1.98 (in, 2H); 1.65 (in, 2H); 1.45 (in, 1H); 1.38 (in, I H); 1. 18-1.00 (in, 8H); 0.85 (in, 6H); 0.78 (d, 3 H) DMSO-d6: 9.25 (s, I H); 8.95 (s, I H); 8.35 9s, I H); 7.72 (bs, 2H); 7.45 83 605.30 4.40 d, 2H); 7.32 (d, 2H); 6.65 (s, 1H); 4.60-4.10 (in, 6H); 3.20 (in, 2H); .05 (s, 3H); 1.98 (in, 2H); 1.65 (in, 2H); 1.45 (in, 1 H); 1.38 (in, 1 H); 1.18-1.00 (in, 8H); 0.85 (in, 6H); 0.78 (d, 3 H) DMSO-d6: 8.98 (bs, I H); 8.94 (s, 1 H); 8.38 (s, 1 H); 7.72 (bs, 2H); 7.45 84 523.30 3.30 (d, 2H); 7.25 (d, 2H); 6.73 (s, I H); 4.60-4.10 (in, 4H); 3.20 (in, 2H); 2.02 (s, 3 H); 1.40 (s, 9H); 1.15 (in, 6H) DMSO-d6: 8.92 (s, I H); 8.32 (d, I H); 8.05 (s, I H); 7.72 (bs, 2h); 7.38 85 494.30 2.40 (d, 2H); 7.22 (d, 2h); 6.63 (in, 111); 6.02 (bs, I H); 4,10-3.55 (in, 6H); 3.40 (in, 2H); 3.00 (t, 2H); 2.00-1.75 (in, 5H); 1.40 (in, 2H); 0.85 (t, 3H) DMSO-d6: 8.92 (s, I H); 8.32 (d, 1 H); 8.05 (s, 1 H); 7.72 (bs, 2h); 7.38 86 494.30 2.40 (d, 2H); 7.22 (d, 2h); 6.63 (in, I H); 6.02 (bs, I H); 4.10-3.55 (in, 7H); 3.40 (in, 2H); 1.75-2.00 (in, 5H); 1.05 (d, 6H) 87 508.30 2.70 DMSO-d6: 8.92 (s, I H); 8.32 (d, I H); 8.05 (s, I H); 7.72 (bs, 2h); 7.38 88 534.30 2.90 (d, 2 H); 7.22 (d, 2h); 6.63 (in, I H); 6.02 (bs, 1 H); 4.10-3.55 (in, 6H); 3.40 (in, 3 H); 1.45-2.10 (in, 10H); 1.35-1.00 (in, 5 H) 89 552.30 2.50 DMSO-d6: 9.25 (bs, I H ); 8.98 (s, I H); 8.38 (s, I H); 7.75 (bs, 2H); 7.42 90 467.20 2.40 (d, 2 H); 7.28 (d, 2 H); 6.60 (in, I H); 4.10-3.55 (in, 6 H); 3.60 (s, 3 H); 3.42 (in, 2H); 2.00-1.75 (in, 5H) DMSO-d6: 9.25 (bs, I H); 8.98 (s, I H); 8.38 (s, I H); 7.75 (bs, 2H); 7.42 91 481.30 2.60 (d, 2H); 7.28 (d, 2H); 6.60 (m, I H); 4.03 (q, 2H); 4.10-3.55 (in, 6H); 3.42 (in, 2 H); 2.00-1.75 (in, 5 H); 1.18 (t, 3 H) DMSO-d6: 9.25 (bs, I H); 8.98 (s, I H); 8.38 (s, I H); 7.75 (bs, 2H); 7.42 92 495.30 2.90 (d, 2H); 7.28 (d, 2H); 6.60 (in, I H); 4.10-3.55 (m, 6H); 3.98 (t, 2H); 3.42 (in, 2H); 2.00-1.75 (in, 5H); 1.58 (m, 2H); 0.93 (t, 3H) DMSO-d6: 9.25 (bs, I H); 8.98 (s, I H); 8.38 (s, I H); 7.75 (bs, 2H); 7.42 93 495.30 2.80 (d, 2H); 7.28 (d, 2H); 6.60 (in, I H); 4.82 (m, I H); 4.10-3.55 (in, 6H); 3.42 (in, 2H); 2.00-1.75 (in, 5H); 1.20 (d, 6H) DMSO-d6: 9.25 (bs, I H); 8.98 (s, 1 H); 8.38 (s, I H); 7.75 (bs, 2H); 7.42 94 509.30 3.10 (d, 2H); 7.28 (d, 2H); 6.60 (m, I H); 4.10-3.55 (in, 6H); 3.60 (d, 2H); 3.42 (in, 2H); 2.00-1.75 (in, 5H); 0.89 (d, 6H) DMSO-d6: 9.25 (bs, I H); 8.98 (s, I H); 8.38 (s, I H); 7.75 (bs, 2H); 7.42 95 523.30 3.30 (d, 2H); 7.28 (d, 2H); 6.60 (in, 1 H); 4.10-3.55 (in, 6H); 3.75 (s, 2H); 3.42 (in, 2H); 2.00-1.75 (in, 5H); 0.91 (s, 9H) 131 Cmpd # LC/MS RT NMR DMSO-d6: 9.85 (bs, I H); 9.05 (bs, I H); 8.32 (d, I H); 7.75 (bs, 2h); 7.50 96 543.30 3.30 (d, 2h); 7.32 (d, 2H); 7.20 (d, 2H); 7.05 (d, 2h); 6.60 (m, lh); 4.10-3.55 (m, 6H); 3.40 (m, 2H); 2.25 (s, 3h); 2.00-1.75 (m, 5H) DMSO-d6: 9.25 (bs, I H); 8.86 (bs, I h); 8.42 (d, I H); 7.75 (bs, 2H); 7.45 97 591.30 3.30 (d, 2H); 7.32 (d, 2H); 6.62 (m, I H); 4.50 (m, I H); 4.10-3.55 (m, 6H); 3.40 (m, 2H); 2.00-1.20 (m, I I H); 1.10-0.72 (m, 12H) DMSO-d6: 9.25 (bs, 1 H); 8.86 (bs, I h); 8.42 (d, 1 H); 7.75 (bs, 2H); 7.45 98 591.30 4.20 (d, 2H); 7.32 (d, 2H); 6.62 (m, I H); 4.50 (m, I H); 4.10-3.55 (m, 6H); 3.40 (m, 2H); 2.00-1.20 (m, I I H); 1.10-0.72 (m, 12H) 8.36 (s, br, I H), 8.11 (s, br, I H), 7.25 (s, br, 2H), 6.90 (d, br, 2H), 6.53 99 422.20 1.51 (d, br, 4H), 4.59 - 3.98 (m, 6H), 3.04 (s, br, 2H), 2.03 (m, 3H), 1.20 S, br, 6H). I H NMR (500 MHz, DMSO-d6) 9.31 (s, br, 1 H), 8.78 (s, br, I H), 8.11 100 522.20 2.41 (d, I H), 7.47 (d, 2H), 7.32 (d, 2H), 7.17 - 6.79 (m, 4H),4.14 (d, 2H), 3.84 (d, 4H), 3.25 (d, 2H), 2.08 (s, 3H), 1.91 (m, I H), 1.23 (s, br, 6H), 0.93 (d, 6H). I H NMR (500 MHz, DMSO-d6) 9.29 (s, br, I H), 8.96 (s, br, I H), 8.10 101 494.20 2.06 (d, 1 H), 7.47 (d, 2H), 7.31 (d, 2 H), 7.06 (s, br, 2 H), 6.90 (s, br, 2 H), 4.09 (m, 3H), 3.23 (d, 2H), 2.08 (s, 3H), 1.23 (m, 12H). I H NMR (500 MHz, DMSO-d6) 9.23 (s, br, 1 H), 8.93 (s, br, I H), 8.12 102 508.20 2.25 (d, I H), 7.47 (d, 2H), 7.29 (d, 2H), 7.04 (s, br, 2H), 6.83 (s, br, 2H), 4.16 (d, 3H), 4.00 (m, 3H), 3.18 (d, br, 2H), 2.07 (s, 3H), 1.63 (m, 2H), 1.22 (s, br, 6H), 0.93 (t, 3H). I H NMR (500 MHz, DMSO-d6) 9.23 (s, br, 1H), 8.94 (s, br, 1H), 8.10 103 508.20 2.20 (d, 1 H), 7.46 (d, 2H), 7.30 (d, 2H), 7.05 (s, br, 2H), 6.87 (s, br, 2H), 4.85 (m, i H), 4.15 (d, 2H), 3.21 (d, br, 2H), 2.08 (s, 3H), 1.24 (m, 14H). 1 H NMR (500 MHz, DMSO-d6) 9.26 (s, br, 1 H), 8.91 (s, br, 104 536.20 2.60 1 H), 8.11 (d, I H), 7.49 (d, 2H), 7.31 (s, br, 2H), 7.01 (s, br, 2H), 6.78 (s, br, 2H), 4.17 (d, 2H), 3.76 (s, 2H), 3.14 M, 2H), 2.07 (s, 3H), 1.22 (m, 7H), 0.94 (m, 10 H). I H NMR (500 MHz, DMSO-d6) 8.88 (s, br, 1 H), 8.16 - 8.05 (m, 2H), 105 493.40 1.80 7.44 (d, 2H), 7.23 (d, 2H), 7.13 - 7.01 (m, 2H), 6.89 (s, br, 1 H), 5.94 (s, br, 1 H), 4.15 (d, 4H), 3.24 (s, br, I H), 3.08 (m, 2H), 2.08 (s, 3H), 1.32 1.11 (m, 8H), 1.04 (t, 3H). I H NMR (500 MHz, DMSO-d6) 8.88 (s, br, 1 H), 8.11 (m, 2H), 7.42 (d, 106 507.40 1.90 2H), 7.22 (d, 2H), 7.06 (s, br, 2H), 6.88 (s, br, I H), 5.99 (s, br, 1 H), 4.17 (d, 4H), 3.22 (s, br, I H), 3.02 (m, 2H), 2.08 (s, 3H), 1.42 (m, 2H), 1.25 (m, 8H), 0.87 (m, 3H). I H NMR (500 MHz, DMSO-d6) 8.87 (s, br, 1H), 8.10 (m, I H), 8.02 (s, 107 507.40 1.90 br, I H), 7.43 (d, 2H), 7.23 (d, 21H), 7.06 (m, 2H), 6.87 (s, br, H), 5.84 (s, br, I H), 4.15 (d, 4 H), 3.74 (m, 1 H), 3.23 (m, I H), 2.07 (s, 3 H), 1.25 (m, 8H), 1.07 (m, 6H). I H NMR (500 MHz, DMSO-d6) 8.85 (s, br, I H), 8.10 (m, I H), 7.97 (s, 108 521.40 2.10 br, I H), 7.42 (d, 2H), 7.20 (m, 2K), 7.05 (m, 2H), 6.87 (s, br, I H), 5.83 (s, br, I H), 4.15 (d, 4H), 3.22 (s, br, 1 H), 2.07 (s, 3H), 1.30 - 1.17 (m, 171H). I H NMR (500 MHz, DMSO-d6) 9.02 (s, br, I H), 8.92 (s, br, I H), 8.1 1 109 522.40 2.40 (d, I H), 7.45 (d, 2H), 7.29 (d, 2H), 7.05 (s, 2H), 6.87 (s, br, 2H) 4.16 (d, 2H ), 3.23 (s, br, 2H), 2.08 (s, 3H), 1.46 (s, 10H), 1.23 (s, br, 7H). 110 520.30 2.51 _| 1 H NMR (500 MHz, DMSO-d6) 9.62 (s, 1 H), 9.00 (s, br, I H), 8.11 (s, 111 506.30 2.41 1 H), 7.48 (dd, 4H), 7.13 - 6.77 (m, 4H), 4.15 (d, 4H), 3.22 (d, br, 2H), .13 (m, 2H), 2.08 (s, 3H), 1.23 (s, br, 6H), 0.93 (m, 7H). DMSO-d6: 9.65 (s, 1 H); 9.02 (s, 1 H); 8.35 (s, 1 H); 7.75 (bs, 2H); 7.52 112 465.40 2.40 (d, 2H); 7.40 (d, 2H); 6.74 (s, 1 H); 4.60-4.00 (m, 4H); 3.20 (m, 2H); 2.05 (s, 3 H); 2.02 (s, 3 H); 1.15 (m, 6H) 132 Cmpd # LC/MS RT NMR 563.30 2.10 1 H NMR (500 MIHz, DMSO-d6) 8.70 (s, 1H), 8.14 (d, I H), 7.44 (d, 2H), 113 563.20 2.03 6.99 - 6.79 (m, 4H), 6.61 (s, br, 2H), 4.20 (d, br, 3H), 4.06 (q, 2H), 3.49 (m, 4H), 3.04 (d, 2H), 2.97 (m, 4H), 2.07 (s, 3 H), 1.20 (m, I OH). DMSO-d6: 9.18 (s, I H); 8.38 (s, I H); 7.76 (bs, 2H); 7.55 (d, 2H); 7.12 114 537.40 3.40 (d, 2H); 6.75 (m, I H); 4.70-4.00 (m, 4H); 3.18 (m, 2H); 3.06 (s, 3H); 2.03 (s, 3 H); 1.32 (s, 9H); 1.15 (m, 6H) DMSO-d6: 9.15 (s, I H); 8.34 (d, I H); 7.72 (bs, 2H); 7.52 (d, 2H); 7.12 115 523.40 3.10 (d, 2H); 6.60 (m, I H); 4.00-3.55 (m, 6H); 3.45-3.35 (m, 2H); 3.12 (s, 3H); 1.95-1.75 (m, 5H); 1.32 (s, 9H) DMSO-d6: 8.60 (s, I H); 8.35 (s, 1 H); 7.68 (bs, 2H); 7.32 (d, 2H); 6.70 116 437.40 1.80 (s, I H); 6.45 (d, 2H); 5.15 (bs, I H); 4.60-4.00 (m, 4H); 3.22 (m, 2H); 2.62 (s, 3 H); 2.02 (s, 3 H); 1. 16 (m, 6H) DMSO-d6: 8.56 (s, 1 H); 8.36 (d, 1 H); 7.65 (bs, 2H); 7.28 (d, 2H); 6.55 117 423.40 1.60 (m, 1 H); 6.45 (d, 2H); 5.15 (bs, 1 H); 4.00-3.55 (m, 6H); 3.45-3.35 (m, 2H); 2.62 (s, 3H); 2.00-1.75 (m, 5H) DMSO-d6: 9.18 (s, 1H); 8.32 (s, H); 7.78 (bs, 2H); 7.58 (d, 2H); 7.15 118 523.40 3.20 (d, 2H); 6.75 (m, 1 H); 4.60-4.00 (m, 4H); 3.88 (q, 2H); 3.22 (m, 2H); 3.18 (s, 3H); 2.02 (s, 3H); 1.55 (m, 2H); 1.18 (m, 6H); 0.72 (m, 3H) DMSO-d6: 9.18 (s, 1H); 8.32 (s, 1 H); 7.78 (bs, 2H); 7.58 (d, 2H); 7.15 119 523.40 3.20 (d, 2H); 6.75 (m, 1 H); 4.78 (m, H); 4.60-4.00 (m, 4H); 3.22 (m, 2H); 3.18 (s, 3H); 2.02 (s, 3H); 1.18 (m, 12H); DMSO-d6: 9.18 (s, 1 H); 8.32 (s, I H); 7.78 (bs, 2H); 7.58 (d, 2H); 7.15 120 537.40 3.40 (d, 2H); 6.75 (m, I H); 4.60-4.00 (m, 4H); 3.75 (d, 2H); 3.22 (m, 2H); 3.18 (s, 3H); 2.02 (s, 3H); 1.76 (m, 1 H); 1.18 (m, 6H); 0.75 (m, 6H); DMSO-d6: 9.22 (s, 1 H); 8.35 (s, 1 H); 7.78 (bs, 2H); 7.65 (d, 2H); 7.32 121 571.40 3.60 (d, 2H); 7.15 (d, 2H); 6.96 (m, 2H); 6.72 (m, I H); 4.60-4.00 (m, 4H); 3.22 (m, 5H); 2.20 (s, 3H); 2.02 (s, 3H); 1.18 (m, 6H) DMSO-d6: 9.85 (s, I H); 8.35 (d, 1 H); 7.68 (bs, 2H); 7.47 (d, 21H); 6.86 122 603.40 2.80 (d, 2H); 6.63 (m, 1 H); 4.00 (m, 2H); 4.00-3.55 (m, 6H); 3.40 (m, 6H); 2.92 (m, 4H); 1.90 (m, 2H); 1.32 (s, 9H) DMSO-d6: 9.80 (s, I H); 8.35 (d, 1 H); 7.66 (bs, 2H); 7.42 (d, 2H); 6.83 123 503.40 1.70 (d, 2H); 6.63 (m, 1 H); 4.00 (m, 2H); 4.00-3.20 (m, 8H); 2.85-2.95 (m, 8H); 1.90 (m, 2H); DMSO-d6: 8.88 (s, 1 H); 8.38 (d, I H); 7.72 (bs, 2H); 7.48 (d, 2H); 6.96 124 575.40 2.50 (d, 2H); 6.62 (m, 1 H); 4.06 (q, 2H); 4.03 (m, 2H); 4.00-3.60 (m, 4H); 3.55-3.35 (m, 8H); 2.92 (m, 4H); 1.85 (m, 21); 1. 15 (t, 3H) DMSO-d6: 8.88 (s, I H); 8.38 (d, I H); 7.72 (bs, 2H); 7.48 (d, 21H); 6.96 125 589.40 2.70 (d, 2H); 6.62 (m, I H); 4.00 (m, 2H); 3.96 (t, 2H); 4.00-3.60 (m, 4H); 3.55-3.35 (m, 8H); 2.92 (m, 4H); 1.85 (m, 2H); 1.58 (m, 2H); 0.82 (t, 3H) DMSO-d6: 9.20 (s, I H); 8.32 (d, I H); 7.75 (bs, 2H); 7.52 (d, 2H); 7.15 126 481.40 2.60 (d, 2H); 6.60 (d, 1 H); 4.10-3.55 (m, 9H); 3.40 (, 2H); 3.12 (s, 3 H); 2.00 1.75 9m, 5H) DMSO-d6: 9.20 (s, I H); 8.32 (d, 1 H); 7.75 (bs, 2H); 7.52 (d, 2H); 7.15 127 495.40 2.80 (d, 2H); 6.60 (d, 1 H); 4.00 (m, 2H); 4.10-3.55 (m, 6H); 3.45 ( 2H); 3.10 (s, 3H); 2.00-1.75 (m, 5H); 1.10 (m, 3H) 1 H NMR (500 MHz, DMSO-d6) 9.08 (s, br, 1 H), 8.11 (d, I H), 7.53 (d, 128 591.30 2.57 2H), 7.15 - 7.01 (m, 6H), 4.14 (d, 3H), 3.83 (d, 2H), 3.59 (s, br, 4H), 3.30 (d, 2H), 3.15 (s, br, 4H), 2.08 (s, 3 H), 1.89 (m, 1 H), 1.23 (s, br, 6H), 0.90 (m, 7H). DMSO-d6: 9.20 (s, 1 H); ,8.32 (d, 1 H); 7.76 (bs, 2H); 7.55 (d, 2H); 7.16 129 509.40 3.00 (d, 2H); 6.60 (m, I H); 3.98 (m, 2H); 4.00-3.55 (m, 6H); 3.55 (m, 2H); 3.10 (s, 3H); 2.00-1.75 (m, 5H); 1.50 (m, 2H); 0.80 (m, 3H) DMSO-d6: 9.20 (s, 1 H); ,8.32 (d, I H); 7.76 (bs, 2H); 7.55 (d, 2H); 7.16 130 509.40 3.00 (d, 2 H); 6.60 (m, 1 H); 4.72 (m, I H); 4.00-3.55 (m, 6H); 3.55 (m, 2 H); 3. 10 (s, 3 H); 2.00-1.75 (m, 5 H); 1.22 (m, 6H) 133 Cmpd # LC/MS RT NMR DMSO-d6: 9.20 (s, I H); ,8.32 (d, 1 H); 7.76 (bs, 2H); 7.55 (d, 2H); 7.16 131 523.40 3.20 (d, 2 H); 6.60 (m, I H); 4.00-3.55 (m, 8 H); 3.55 (,. 2 H); 3.12 (s, 3 H); 2.00-1.75 (m, 6H); 0.80 *m, 6H) DMSO-d6: 9.20 (s, 1 H); 8.32 (d, I H); 7.76 (bs, 2H); 7.55 (d, 2H); 7.16 132 537.40 3.40 (d, 2H); 6.60 (m, I H); 4.00-3.55 (m, 8H); 3.55 (m, 2H); 3.12 (s, 3H); 2.00-1.75 (m, 5H); 0.70 (m, 9H) DMSO-d6: 9.22 (s, 1 H); 8.32 (d, 1 H); 7.72 (bs, 2H); 7.58 (d, 2H); 7.25 133 557.30 3.40 (d, 2H); 7.15 (d, 2H); 6.98 (m, 2H); 6.60 (m, I H); 4.00-3.55 (m, 6H); 3.40 (m, 2H);; 3.20 (m, 3H); 2.20 (s, 3H); 2.00-1.75 (m, 5H) DMSO-d6: 9.22 (s, 1 H); 8.40 (d, 1 H); 7.70 (bs, 2H); 7.62 (d, 2H); 7.30 134 543.30 3.20 (m, 4H); 7.18 (m, 1 H); 7.10 (m, 2H); 6.60 (m, i H); 4.00-3.55 (m, 6H); 3.40 (m, 2H); 3.28 (m, 3 H); 2.00-1.75 (m, 5 H) DMSO-d6: 9.22 (s, I H); 8.34 (d, I H); 7.70 (bs, 2H); 7.62 (d, 2H); 7.20 135 573.30 3.20 (m, 2H); 7.00 (m, 2H); 6.90 (m, 2H); 6.62 (m, 1 H); 4.00-3.55 (m, 9H); 3.40 (m, 2H); 3.25 (m, 3H); 2.00-1.75 (m, 5H) DMSO-d6: 9.02 (bs, I H); 8.92 (s, I H); 8.40 (d, I H); 7.62 (bs, 2H); 7.40 136 534.30 3.10 (d, 2H); 7.30 (d, 2H); 6.62 (m, 1H); 4.10-3.55 (m, 8H); 3.40 (m, 2H); 1.86 (m, 2H); 1.40 (s, 9H) DMSO-d6: 9.32 (s, 1 H); 8.95 (s, I H); 8.32 (d, 1 H); 7.75 (bs, 2H); 7.42 137 506.40 2.70 (d, 2H); 7.25 (d, 2H); 6.65 (m, 1 H); 4.05 (q, 2H); 4.00 (m, 2H); 4.00 3.40 (m, 8H); 1.85 (m, 2H); 1.15 (t, 3H) DMSO-d6: 9.88 (bs, 1 H); 9.05 (s, 1 H); 8.35 (d, I H); 7.75 (bs, 2H); 7.50 138 568.40 3.30 (d, 2H); 7.32 (d, 2H); 7.18 (d, 2H); 7.02 (d, 2H); 6.62 (m, I H); 3.98 (m, 2H); 4.00-3.30 (m, 8H); 2.29 (s, 3H); 1.88 (m, 2H); 1H NMR (500 MHz, CD30D) 8.04 (d, 1H), 7.65 (s, br, 2H), 7.37 (m, 139 577.20 2.31 4H), 4.13 - 3.98 (m, 4H), 3.82 (s, br, 4H), 3.61 - 3.32 (m, 5H), 2.65 (s, 8H), 2.20 (s, 3H), 1.70 (m, 2H), 1.38 (s, br, 4H), 0.98 (t, 3H). I H NM R (500 MHz, CD30D) 7.99 (m, I H), 7.64 (m, 2H), 7.41 - 7.22 140 588.20 2.10 (m, 4H), 4.08 (t, 2H), 4.04 - 3.71 (m, 12H), 3.66 (m, 2H), 3.43 (s, br, 3H ), 2.65 (s, 4H), 2.03 (s, br, 2H), 1.69 (m, 2H), 0.98 (t, 3H). DMSO-d6: 8.95 (m, I H); 8.05 (m, 1 H); 7.50 (m, 2H); 7.05 (m, I H); 141 574.30 2.80 6.90 (m, 5H); 4.00 (m, 4H); 4.00-3.50 (m, 4H); 3.00 (m, 4H); 1.85 (m, 2 H); 1.22 (t, 3 H) 1 H NMR (500 MHz, DMSO-d6) 9.11 (s, br, I H), 8.11 (d, 1 H), 7.53 (d, 142 605.30 2.00 2H), 7.17 - 6.96 (m, 6H), 4.14 (d, 2H), 3.75 (s, 2H), 3.61 (s, br, 5H), 3.31 (d, 2H), 3.17 (s, br, 4H), 2.08 (s, 3H), 1.24 (s, br, 6H), 0.93 (s, 10 H). I H NMR (500 MHz, DMSO-d6) 8.99 (s, br, I H), 8.11 (d, I H), 143 577.30 2.22 7.50 (d, 2H), 7.13 - 6.84 (m, 6H), 4.80 (m, 1 H), 4.14 (d, 2H), 3.54 (s, br, 5 H), 3.25 (d, br, 2H), 3.09 (s, br, 4H), 2.08 (s, 3 H), 1.20 (m, 13 H). DMSO-d6: 9.02 (bs, I H); 8.08 (d, I H); 7.52 (d, 2H); 7.15 (m, I H); 6.98 144 585.40 2.20 (m, 5H) 4.05 (q, 2H); 3.85 (m, 4H); 3.55 (m, 6H); 3.35 (m, 2H); 3.12 (m, 4H); 2.88 (s, 3 H); 1.90 (m, 2H); 1. 15 (t, 3 H) 145 599.40 2.30 146 613.50 2.10 DMSO-d6: 8.95 (bs, I H); 8.06 (d, I H); 7.42 (i, 2H); 7.10-6.90 (m, 6H); 147 627.50 2.30 4.05 (q, 2h); 3.82 (m, 4H); 3.52 (m, 6H); 3.28 (m, 2H); 3.05 (m, 6H); 1.88 (m, 2H); 1.52 (m, 2H); 1.25 (m, 2H); 1.20 (t, 3H); 0.80 (t, 3H) DMSO-d6: 8.95 (bs, I H); 8.06 (d, 1 H); 7.48 (m, 2H); 7.10-6.90 (m, 6H); 148 565.40 2.30 4.06 (q, 2 H); 3.80 (m, 4 H); 3.60 (m, 2 H); 3.55 (s, 3 H); 3.50 (m, 4 H); 3.35 (m, 2H); 3.00 (m, 4H); 1.80 (m, 2H); 1.16 (t, 3H) 149 579.40 2.40 8.95 (bs, 1 H); 8.02 (d, 1 H); 7.42 (m, 2H); 7.10-6.90 (m, 6h); 4.05 (q, 150 593.50 2.20 2H); 3.80-3.40 (m, 14H); 3.00 (m, 4H); 1.85 (m, 2H); 1.35 (m, 2H); 1.20 (m, 3H); 0.75 (m, 3H) 8.95 (bs, 1 H); 8.02 (d, I H); 7.42 (m, 2 H); 7.10-6.90 (m, 6h); 4.62 (m, 151 593.50 2.30 1 H); 4.02 (q, 2H); 3.80 (m, 4H); 3.60-3.40 (m, 8H); 3.02 (m, 4H); 1.80 in,2H); 1.20 (t, 3 H); 1.02 (m, 6H) 134 Cmpd # LC/MS RT NMR 152 585.30 2.00 153 599.30 2.10 DMS)-d6: 8.96 (bs, I H); 8.03 (d, I H); 7.42 (d, 2H); 7.20-6.80 (m, 6H); 154 613.30 2.30 3.80-3.60 (m, 81H); 3.40 (m, 21H); 3.35 (m, 41H); 3.10 (m, 6H); 1.85 (m, 2H); 1.45 (m, 2H); 1.22 (m, 3H); 0.80 (m, 3H) DMS)-d6: 8.96 (bs, I H); 8.03 (d, I H); 7.42 (d, 2H); 7.20-6.80 (m, 6H); 155 613.30 2.30 4.60 (m, I H); 3.90-3.10 (m, 6H); 3.32 (m, 6H); 3.12 (m, 6H); 1.80 (m, 2H); 1.22 (m, 3H); 1.06 (m, 6H) I H NMR (500 MHz, CD30D) 7.98 (m, I H), 7.69 (s, br, 2H), 7.51 - 7.33 156 579.20 1.70 (m, 3 H), 7.28 (s, br, I H), 4.94 (m, I H), 3.97 -3.78 (m, I OH), 3.63 (s, br, 3H), 3.60 - 3.42 (m, 6H), 1.96 (s, br, 2H), 1.30 (d, 6H). I H NMR (500 MHz, CD30D) 7.99 (m, I H), 7.69 (s, br, 2H), 7.51 - 7.34 157 593.20 1.80 (m, 3H), 7.28 (s, br, I H), 4.93 (m, I H), 4.11 - 3.98 (m, 2H), 3.98 - 3.77 (m, 10 H), 3.63 - 3.37 (m, 6H), 1.97 (s, br, 2H), 1.28 (d, 6H), 1.15 (m, 3 H). I H NMR (500 MHz, DMSO-d6) 9.04 (s, br, 1 H), 8.07 (d, I H), 7.50 (d, 158 579.20 1.70 2H), 7.18 - 6.96 (m, 6H), 3.99 (t, 2H), 3.87 - 3.76 (m, 4H), 3.65 (m, 2H), 3.60 - 3.49 (m, 8H), 3.41 (s, br, 2H), 3.08 (s,br, 3H), 1.85 (m, 2H), 1.59 (m, 2H), 0.91 (t, 3H). I H NMR (500 MHz, DMSO-d6) 9.01 (s, br, I H), 8.06 (d, I H), 7.49 (d, 159 593.20 1.80 2H), 7.16 - 6.92 (m, 6H), 3.99 (t, 2H), 3.87 - 3.77 (m, 4H), 3.65 (s, br,2H), 3.54(s, br, 5H), 3.41 (s, br, 2H), 3.06 (s, br, 4H), 1.84 (s, br, 2H), 1.59 (m, 2H), 1.07 (m, 4H), 0.91 (t, 3H). 160 607.20 1.90 161 607.20 1.90 1 H NMR (500 MHz, DMSO-d6) 9.03 (s, br, I H), 8.08 (d, I H), 7.50 (d, 162 599.20 1.70 2H), 7.20 - 6.89 (m, 6H), 4.00 (t, 2H), 3.92 - 3.80 (m, 4H), 3.55 (m, 8H), 3.09 (s, br, 4H), 2.90 (s, 3H), 1.92 (m, 2H), 1.60 (m, 2H), 0.90 (t, 3 H). 163 613.20 1.70 164 627.20 1.90 165 627.20 1.80 DMSO-d6: 9.60 (bs, I H); 8.95 (bs, I H); 8.40 (s, I H); 7.50 (d, 2H); 6.92 166 548.30 2.00 (d, 2H); 6.72 (s, 1 H); 4.10-3.90 (m, 6H); 3.75 (m, 3 H); 3.50 (m, 4H); 3.00 (m, 4H); 2.82 (d, 3h); 2.38 (i, 2H); 2.15 (m, I H); 1.88 (m, 2H); 1.15 (t, 3h) DMSO-d6: 8.99 (bs, I H); 8.32 (bs, I H); 7.75 (bs,2H); 7.50 (m, 2H); 167 439.30 2.10 7.05 (m, 2 H); 6.60 (m, I H); 4.06 (q, 2 H); 3.55 (m, 4 H); 3.10 (m, 4 H); 2.80 (s, 3H); 1.22 (t, 3H) I H NMR (500MHz, CD30D) 7.98 (d, I H), 7.64 (d, 2H), 7.40 - 7.27 (m, 168 599.10 1.60 4H), 4.99 (m, I H), 3.97 (s, br, 3H), 3.79 (s, br, 3H), 3.70 (t, 2H), 3.53 3.37 (m, 6H), 2.99 (s, I H), 2.92 (s, 2H), 2.86 (s, I HI), 2.82 (s, I H), 2.35 (t, I H), 2.04 (m, 2H), 1.28 (m, 5H). I H NMR (500 MHz, CD30D) 7.99 (d, I H), 7.65 (d, 2H), 7.39 - 7.25 169 613.20 1.70 (m, 4H), 4.93 (m, I H), 3.93 (m, 4H), 3.80 (m, 4H), 3.73 (t, 2H), 3.53 3.39 (m, 6H), 3.11 (m, 2H), 2.03 (m, 21H), 1.28 (m, 9H). DMSO-d6: 9.30 (bs, I H); 9.02 (m, I H); 8.03 (m, I H); 7.42 (d, 2H); 7.28 170 465.90 2.39 (d, 2H); 7.10-6.90 (m, 3h); 3.80-3.60 (m, 6H); 3.60 (s, 3h); 3.50-3.40 (m, 2h); 1.95 (m, 3H); 1.85 (m, 2H) DMSO-d6: 9.30 (bs, I H); 9.02 (m, I H); 8.03 (m, 1 H); 7.42 (d, 2H); 7.28 171 479.90 2.67 (d, 2H); 7.10-6.90 (m, 3H); 4.04 (q, 2H); 3.80 (m, 6H); 3.50-3.40 (m, 2H); 1.95 (m, 3H); 1.85 (m, 2H); 1.22 (t, 3H) DMSO-d6: 9.30 (bs, IH); 9.02 (m, IH); 8.03 (m, 1H); 7.42 (d, 2H); 7.28 172 493.90 3.03 (d, 2H); 7.10-6.90 (m, 3H); 3.98 (t, 2H); 3.90-3.60 (m, 6H); 3.50-3.40 (m, 2H); 1.95 (m, 3H); 1.85 (m, 2H); 1.60 (m, 2H); 0.90 (t, 3H) DMSO-d6: 9.30 (bs, I H); 9.02 (m, I H); 8.03 (m, 1 H); 7.42 (d, 2H); 7.28 173 493.90 2.97 (d, 2H); 7.10-6.90 (m, 3H); 4.82 (m, I H); 3.90-3.60 (m, 6H); 3.50-3.40 (m, 2H); 1.95 (m, 3H); 1.85 (m, 2H); 1.22 (d, 6H) 135 Cmpd # LC/MS RT NMR DMSO-d6: 9.30 (bs, I H); 9.02 (m, I H); 8.03 (m, I H); 7.42 (d, 2H); 7.28 174 507.90 3.40 (d, 2H); 7.10-6.90 (m, 3H); 4.02 (t, 2H); 3.90-3.60 (m, 6H); 3.50-3.40 (m, 2H); 1.95 (m, 3H); 1.85 (m, 2H); 1.60 (m, 2h0; 1.36 9m, 2H); 0.90 (t, 3H) DMSO-d6: 9.30 (bs, I H); 9.02 (m, I H); 8.03 (m, I H); 7.42 (d, 2H); 7.28 175 507.90 3.38 (d, 2H); 7.10-6.90 (m, 3H); 3.90-3.60 (m, 6H); 3.80 (d, 2H); 3.50-3.40 (m, 2H); 1.95 (m, 3H); 1.85 (m, 3H); 0.89 (d, 6H) DMSO-d6: 9.30 (bs, I H); 9.02 (m, I H); 8.03 (m, I H); 7.42 (d, 2H); 7.28 176 522.00 3.70 (d, 2H); 7.10-6.90 (m, 3H); 4.00-3.30 (m, IOH); 1.95-1.85 (m, 5H); 0.88 (s, 9H) 1001291 Example 22. Inhibition of FLT-3: 1001301 Compounds were screened for their ability to inhibit FLT-3 activity using a radiometric filter-binding assay. This assay monitors the 3 3 P incorporation into a substrate poly(Glu, Tyr) 4:1 (pE4Y). Reactions were carried out in a solution containing 100 mM HEPES (pH 7.5), 10 mM MgCl 2 , 25 mM NaCl, 1 mM DTT, 0.01% BSA and 2.5% DMSO. Final substrate concentrations in the assay were 90 iM ATP and 0.5mg/mL pE4Y (both from Sigma Chemicals, St Louis, MO). The final concentration of compounds is generally between 0.01 and 5 pM. Typically, a 12-point titration was conducted by preparing serial dilutions from 10 mM DMSO stock of test compound. Reactions were carried out at room temperature. Solution 1 contains 100 mM HEPES (pH 7.5), 10 mM MgCl 2 , 25 mM NaCl, I mg/ml pE4Y and 180 ptM ATP(containing 0.3 ptCi of [y- P]ATP for each reaction). Solution 2 contains 100 mM HEPES (pH 7.5), 10 mM MgC 2 , 25 mM NaCl, 2 mM DTT, 0.02% BSA and 3 nM FLT-3. The assay was run on a 96 well plate by mixing 50 jiL each of Solution 1 and 2.5 mL of the test compounds. The reaction was initiated with Solution 2. After incubation for 20 minutes at room temperature, the reaction was stopped with 50 ptL of 20% TCA containing 0.4mM of ATP. All of the reaction volume was then transferred to a filter plate and washed with 5% TCA by a Harvester9600 from TOMTEC (Hamden, CT). The amount of 33 P incorporation into pE4y was analyzed by a Packard TopCount Microplate Scintillation Counter (Meriden, CT). The data was fitted using Prism software to get an IC 50 or Ki. 1001311 Many compounds of the invention, including compounds in Table 1, inhibited FLT-3. 1001321 Example 23: Inhibition of AUR-2: 1001331 Compounds are screened in the following manner for their ability to inhibit Aurora 2 using a standard coupled enzyme assay (Fox et al (1998) Protein Sci 7, 2249). To an assay stock buffer solution containing 0.l M HEPES 7.5, 10 mM MgCl 2 , 1 mM DTT, 25 mM NaCl, 2.5 mM phosphoenolpyruvate, 300 mM NADH, 30 mg/ml pyruvate kinase, 10 mg/ml lactate 136 dehydrogenase, 40 mM ATP, and 800 pM peptide (LRRASLG, American Peptide, Sunnyvale, CA) is added a DMSO solution of a compound of the present invention to a final concentration of 30 pM. The resulting mixture is incubated at 30 "C for 10 min. The reaction was initiated by the addition of 10 pL of Aurora-2 stock solution to give a final concentration of 70 nM in the assay. The rates of reaction are obtained by monitoring absorbance at 340 nm over a 5 minute read time at 30 'C using a BioRad Ultramark plate reader (Hercules, CA). The Ki values are determined from the rate data as a function of inhibitor concentration. 1001341 Many compounds of the invention, including compounds in Table 1, inhibited AUR 2 with a Ki of less than 50 nM. 1001351 Example 24: Inhibition of KDR [001361 Compounds were screened for their ability to inhibit KDR using a standard coupled enzyme assay (Fox et al., Protein Sci., (1998) 7, 2249). Assays were carried out in a mixture of 200 mM HEPES 7.5, 10 mM MgCl2, 25 mM NaCI, 1 mM DTT and 1.5% DMSO. Final substrate concentrations in the assay were 300pM ATP (Sigma Chemicals) and 10 pM poly E4Y (Sigma). Assays were carried out at 37 "C and 30 nM KDR. Final concentrations of the components of the coupled enzyme system were 2.5 mM phosphoenolpyruvate, 200 pM NADH, 30 pg/ML pyruvate kinase and 10 ptg/ml lactate dehydrogenase. An assay stock buffer solution was prepared containing all of the reagents listed above, with the exception of ATP and the test compound of interest. 177 tl of the stock solution was placed in a 96 well plate followed by addition of 3 tl of 2 mM DMSO stock containing the test compound (final compound concentration 30 pM). The plate was preincubated for about 10 minutes at 37 "C and the reaction initiated by addition of 20 pl of ATP (final concentration 300 pM). Rates of reaction were obtained using a Molecular Devices plate reader (Sunnyvale, CA) over a 5 minute read time at 37"C. Compounds showing greater than 50% inhibition versus standard wells containing the assay mixture and DMSO without test compound were titrated to determine IC50 values determined. 100137] Some compounds of the invention, including compounds in Table 1, inhibited KDR with a Ki of less than 50 nM. 1001381 Example 25. JAK3 Inhibition Assay 1001391 Compounds were screened for their ability to inhibit JAK using the assay shown below. Reactions were carried out in a kinase buffer containing 100 mM HEPES (pH 7.4), 1 mM DTT, 10 mM MgCl 2 , 25 mM NaCl, and 0.01% BSA. 1001401 Substrate concentrations in the assay were 5 pM ATP (200 uCi/pmole ATP) and I pM poly(Glu) 4 Tyr. Reactions were carried out at 25'C and 1 nM JAK3. 137 [001411 To each well of a 96 well polycarbonate plate was added 1.5 p1 of a candidate JAK3 inhibitor along with 50 pl of kinase buffer containing 2 pM poly(Glu) 4 Tyr and 10 pM ATP. This was then mixed and 50pl of kinase buffer containing 2 nM JAK3 enzyme was added to start the reaction. After 20 minutes at room temperature (25'C), the reaction was stopped with 50p of 20% trichloroacetic acid (TCA) that also contained 0.4 mM ATP. The entire contents of each well were then transferred to a 96 well glass fiber filter plate using a TomTek Cell Harvester. After washing, 60 pl of scintillation fluid was added and 33 P incorporation detected on a Perkin Elmer TopCount. [00142] Example 26. JAK2 Inhibition Assay [00143] The assays were as described above in Example 25 except that JAK-2 enzyme was used, the final poly(Glu) 4 Tyr concentration was 15 pM, and final ATP concentration was 12 pM. [001441 Table 3 depicts JAK2 and JAK3 inhibition data (Ki) for exemplary compounds. Compound numbers in Table 3 corresponds to those compounds depicted in Table 1. In Table 3, "A" represents a Ki of less than 0.05 pM and "B" represents a Ki of between 0.05 and 0.5 pM for the indicated enzyme. Table 3 Cmpd # JAK2 JAK3 Cmpd# JAK2 JAK3 Cmpd # JAK2 JAK3 I B A 60 A A 119 A A 2 A A 61 A A 120 A A 3 A A 62 A A 121 A A 4 A A 63 A A 122 A A 5 A A 64 A A 123 A A 6 A A 65 A A 124 A A 7 A A 66 A A 125 A A 8 A A 67 A A 126 A A 9 A A 68 A A 127 A A 10 A A 69 A A 128 A A II A A 70 A A 129 A A 12 A A 71 A A 130 A A 13 A A 72 A A 131 A A 14 B B 73 A A 132 A A 15 A A 74 A A 133 A A 16 A A 75 A A 134 A A 17 A A 76 A A 135 A A 18 A A 77 A A 136 A A 19 A A 78 A A 137 A A 20 A A 79 A A 138 A A 21 A A 80 A A 139 A A 22 A A 81 A A 140 A A 23 A A 82 A B 141 24 A A 83 A N 142 A A 25 B B 84 A A 143 A A 26 A A 85 A A 144 B B 27 A A 86 A A 145 B B 138 Cp# JAK2 JAK3 Cmd JAK2 JAK3 Cmpd# JAK2 JAK3 28 A A 87 A A 146 B B 29 A A 88 A A 147 B B 30 A A 89 A A 148 B B 31 A A 90 A A 149 B B 32 A A 91 A A 150 B B 33 A A 92 A A 151 B B 34 A A 93 A A 152 B B 35 A A 94 A A 153 B B 36 A A 95 A A 154 B B 37 A A 96 A A 155 B B 38 A A 97 B B 156 B B 39 A A 98 B B 157 B B 40 A A 99 A A 158 B B 41 A A 100 A A 159 B B 42 A A 101 A A 160 B B 43 A A 102 A A 161 B B 44 A A 103 A A 162 B B 45 A A 104 A A 163 B B 46 A A 105 A A 164 B B 47 A A 106 A A 165 B B 48 A A 107 A A 166 A A 49 A A 108 A A 167 A A 50 A A 109 A A 168 B B 51 A A 110 A A 169 B B 52 A A III A A 170 B B 53 A A 112 A A 171 B A 54 A A 113 A A 172 B A 55 A A 114 A A 173 B A 56 A A 115 A A 174 B B 57 A A 116 A A 175 B B 58 A A 117 A A 176 B B 59 A A 118 A A 119 A A [00145] While a number of embodiments of this invention have been described, it is apparent that our basic examples may be altered to provide other embodiments which utilize the compounds and methods of this invention. Therefore, it will be appreciated that the scope of this invention is to be defined by the appended claims rather than by the specific embodiments that have been represented by way of example above. [001461 The term "comprise" and variants of the term such as "comprises" or "comprising" are used herein to denote the inclusion of a stated integer or stated integers but not to exclude any other integer or any other integers, unless in the context or usage an exclusive interpretation of the term is required. 1001471 Any reference to publications cited in this specification is not an admission that the disclosures constitute common general knowledge in Australia. 139

Claims (19)

1. 2. The compound according to claim 1, wherein RX is selected from N N N 0N Ro NO H n 0cI )-iH N R'O N O R N O NRN N RO R O O R" 0 N R .
2. 3. The compound according to claim 1, wherein R is H 3 C CH 3
3. 4. The compound according to any one of claims 1-3, wherein A is N.
4. 5. The compound according to any one of claims 1-3, wherein A is Cl-. 142
5. 6. The compound according to any one of claims 1-3, wherein R' is a CI- 6 aliphatic, phenyl or a 5-8 membered heteroaryl group, wherein R' is optionally substituted with up to one occurrence of J.
6. 7. The compound according to claim 6, wherein R' is a CI- 6 aliphatic group or phenyl, wherein R' is optionally substituted with up to one occurrence of J, wherein J is -COOR', -OR', R' or -CF 3 , and wherein R 0 is a C 1 . 3 aliphatic group.
7. 8. The compound according to claim 7, wherein R' is methyl, ethyl, propyl, isopropyl, -CH 2 -isopropyl, butyl, t-butyl, -CH 2 -t-butyl or cyclohexyl, wherein R' is optionally substituted with -COOR', -OR' or R'.
8. 9. The compound according to any one of claims 1-3, wherein R is hydrogen or methyl.
9. 10. The compound according to any one of claims 1-3, wherein each R" is independently selected from a CI- 6 aliphatic group, phenyl or a 5-8 membered heterocycle group, wherein each R" is optionally and independently substituted with up to one occurrence of J.
10. 11. The compound according to claim 10, wherein each R" is independently selected from a C 1 - 6 aliphatic group or phenyl, wherein each R" is optionally and substituted with up to one occurrence of J, wherein each J is independently selected from halogen, -CF 3 , -CN, -COOR, -COR 0 or -OR', wherein each R' is a Ci. 3 aliphatic group.
11. 12. The compound according to claim 11, wherein each R" is methyl, ethyl, propyl, isopropyl, -CH 2 -isopropyl, butyl, t-butyl or -CH 2 -t-butyl, wherein each R" is optionally substituted with -CN, -COOR 0 or -OR'.
12. 13. A compound selected from one of the compounds in Table 1.
13. 14. A composition comprising the compound according to any one of claims 1-13 and a pharmaceutically acceptable carrier, adjuvant, or vehicle.
14. 15. The composition according to claim 14, further comprising an additional therapeutic agent selected from a chemotherapeutic or anti-proliferative agent, an anti inflammatory agent, an immunomodulatory or immunosuppressive agent, a neurotrophic factor, 143 an agent for treating cardiovascular disease, an agent for treating diabetes, or an agent for treating immunodeficiency disorders.
15. 16. The composition according to claim 15, wherein said therapeutic agent is an immunomodulatory or immunosuppressive agent.
16. 17. A method of inhibiting JAK2 or JAK3 kinase activity in a biological sample, comprising contacting said biological sample with the compound according to any one of claims 1-13 or a composition thereof.
17. 18. A method of treating or lessening the severity of a disease of condition selected from an allergy, asthma, an autoimmune disease, transplant rejection, (AML, Lou Gehrig's disease), multiple sclerosis (MS), a solid malignancy, a hematologic malignancy or a myeloproliferative disorder in a patient, comprising administering to said patient a compound according to any one of claims 1-13 or a composition thereof.
18. 19. The method of claim 18, comprising the additional step of administering to said patient an additional therapeutic agent selected from a chemotherapeutic or anti-proliferative agent, an anti-inflammatory agent, an immunomodulatory or immunosuppressive agent or a neurotrophic factor, wherein said additional therapeutic agent is appropriate for the disease being treated.
19. 20. The method according to claim 18, wherein the disease or disorder is allergic or type I hypersensitivity reactions, asthma, amyotrophic lateral sclerosis (AML, Lou Gehrig's disease), multiple sclerosis (MS), transplant rejection, graft versus host disease, rheumatoid arthritis, leukemia, lymphoma, polycythemia vera, essential thrombocythemia, chronic idiopathic myelofibrosis, myeloid metaplasia with myelofibrosis, chronic myeloid leukemia, chronic myelomonocytic leukemia, chronic eosinophilic leukemia, hypereosinophilic syndrome or systematic mast cell disease. Date: 13 July 2012 144