WO2006017443A2

WO2006017443A2 - Aryl-amino substituted pyrrolopyrimidine multi-kinase inhibiting compounds

Info

Publication number: WO2006017443A2
Application number: PCT/US2005/027274
Authority: WO
Inventors: Saleh Ahmed; Oscar Barba; Jason Bloxham; Graham Dawson; William Gattrell; John Kitchin; Neil Anthony Pegg; Imaad Saba; Shazia Sadiq; Colin Peter Sambrook Smith; Don Smyth; Arno G. Steinig; Robin Wilkes; Kenneth Foreman; Qinghua Felix Weng; Kathryn Stolz; Paula Tavares; Bijoy Panicker; An-Hu Li; Hanqing Dong
Original assignee: Osi Pharmaceuticals, Inc.
Priority date: 2004-08-02
Filing date: 2005-08-01
Publication date: 2006-02-16
Also published as: EP1797054A2; WO2006017443A3; JP2008508358A; TW200615268A; BRPI0514094A; US20060211678A1; US7465726B2; MX2007001399A; CA2575808A1; AR050365A1

Abstract

Compounds represented by Formula (I): or stereoisomers or pharmaceutically acceptable salts thereof, are inhibitors of least two of the Abl, Aurora-A, Blk, c-Raf, cSRC, Src, PRK2, FGFR3, Flt3, Lck, Mekl, PDK-1, GSK3ß, EGFR, p70S6K, BMX, SGK, CaMKII, Tie-2, IGF-lR, Ron, Ret, and KDR kinases in animals, including humans, for the treatment and/or prevention of various diseases and conditions such as cancer.

Description

TITLE OF THE INVENTION

ARYL-AMINO SUBSTITUTED PYRROLOPYRIMIDINE MULTI-KTNASE INHIBITING COMPOUNDS

BACKGROUND OF THE INVENTION

[1] The present invention is directed to novel pyrrolopyrimidine compounds, their salts, and compositions comprising them. In particular, the present invention is directed to novel aryl-amino substituted pyrrolopyrimidine compounds that inhibit the activity of at least two of the AbI, Aurora-A, BIk, c-Raf, cSRC, Src, PRK2, FGFR3, Flt3, Lck, Mekl, PDK-I, GSK3/3, EGFR, p70S6K, BMX, SGK, CaMKII, Tie-2, Ret, IGF-IR, Ron, and KDR kinases in animals, including humans, for the treatment and/or prevention of various diseases and conditions such as cancer.

[2] Cells may migrate and divide inappropriately if the signals for division or motility cannot be stopped. This might occur if the complex system of control proteins and messengers, which signal changes in the actin system, goes awry. One such control factor is the proto-oncogene protein AbI, a tyrosine kinase. It is implicated in cancer, including leukemia. Accordingly, it is desirable to identify inhibitors of AbI. [3] The Aurora kinase family is one regulator of chromosome segregation - regulating the structure and function of centrosomes and mitotic spindle. One member, the Aurora-A kinase, has been shown to play a role in tumorigenesis - being located at a chromosomal hot-spot, 20ql3, frequently amplified in a variety of human cancers such as those of colon, ovary, breast and pancreas. It appears that overexpression of Aurora-A kinase alone is sufficient to cause aneupoidy in normal diploid epithelial cells. Over-expression of Aurora-A kinase in NIH3T3 cells results in centrosome aneupoidy. Thus, it is desirable to identify inhibitors of Aurora-A.

[4] Shortly after birth, mice expressing an activated, mutant form of BIk form massive, monoclonal lymphomas and die. (S.V. Desiderio ath. Hughs Medical Institute). Thus, it is likely that BIk regulates cell proliferation. Further, experiments with BIk antisense appear to implicate BIk kinase with growth inhibition and apoptosis. (X.Yao and D.W. Scott, Proc. Nat. Acad. Sci., 90:7946-7950(1993)). Thus, it is desirable to identify inhibitors of BIk. [5] C-Raf is an extracellular signal-regulated kinase and a downstream effector of Ras. It functions to suppress apoptosis and regulates cell differentiation. Thus, over- expression can lead to unwarranted suppression of apoptosis and unchecked cell differentiation. Thus, it is desirable to identify inhibitors of c-Raf. [6] The cytoplasmic tyrosine kinase cSRC, or c-Src, is involved in the signal transduction pathway and is elevated in breast cancer cell lines. Similarly, Src is involved in the regulation of cell growth and transformation. Thus over-expression of Src or cSRC can lead to excess proliferation. Thus, it is desirable to identify inhibitors of Src or c-SRC.

[7] The Protein Kinase c-Related Kinase 2, or PRK2, mediates cytoskeletal organization. It has been implicated in promoting the PDKl -dependent activation of Alct, thereby regulating cell-cycle progression, cell growth, cell survival, cell motility and adhesion, translation of mRNA into protein, and angiogenesis. Thus, it is desirable to identify inhibitors of PRK2.

[8] FGFR3 and Tie-2 are receptor tyrosine kinases that are believed to be important mediators of tumor angiogenesis. For example, FGFR3 mutations are often seen in bladder cancer cells. Tie-2 is a protein receptor found on cells lining blood vessels. When activated by growth factors secreted by tumor cells, Tie2 triggers vessel cell walls to part and grow new capillaries. Thus, it is desirable to identify inhibitors of FGFR3 or Tie-2.

Flt3, also known as "vascular endothelial cell growth factor receptor 3" or VEGFR-3, is believed to assist in vascular development important to angiogenesis. Thus, it is desirable to identify inhibitors of Flt3.

[9] Lck, along with fyn, is an Src kinase implicated in cancer, including breast and colon cancer. Accordingly, it is desirable to identify inhibitors of Lck. flO] Mekl is a kinase in the Ras pathway strongly implicated in many cancers, including breast, colon, and ovarian cancer. Thus, it is desirable to identify inhibitors of

Mekl.

[11] PDK-I is a kinase that activates the PI3K/PKB signalling pathway, which is often uncoupled and separate from the EGFR pathway. In particular, a PDK-I phosphorylating step is essential to activation of PKB (D.R. Alessi et al., Curr. Biol., 7:261-

269(1997)). Additionally, PDK-I activates other oncogene kinases such as PKA, ribosomal p90 S6 kinase (RSK), p70 S6 kinase (S6K), serum and glucocorticoid activated kinase

(SGK), PKC-related kinase-2 (PRK-2) and MSK-I (R.M. Biondi et al., Biochem. J., 372:1-

13(2003)). Thus, inhibition of PDK-I can be multiply effective in treatment of cancer and tumors, including glioblastoma, melanoma, prostate, endometrial carcinoma, breast, ovarian, and non-small cell lung cancer (NSCLC), because PDK-I regulates several oncogenic pathways. Accordingly, it is desirable to identify compounds that inhibit PDK-I .

[12] GSK3/3 kinase is believed to play a strong part in cancers such as breast, ovarian, pancreatic, and prostate cancer. Thus, it is desirable to identify compounds that inhibit GSK3/3.

[13] Cell division involves signalling pathways from the cell exterior and interior.

Signals travel the pathways and regulate the various activities of cell cycle control genes.

Cancer cells have mis-regulation of such signal pathways and control genes - thereby leading to inappropriate or uncontrolled cell division. Over-expression of oncogenes (proteins that signal cells to proliferate) is one such mis-regulation. The Epidermal Growth Factor Receptor (EGFR) is one such oncogene, which is over-expressed in cancers such as brain, breast, gastrointestinal, lung, ovary and prostate cancers. There are selective EGFR inhibitors being investigated for use against cancer. For example, the 4-anilinoquinazoline compound Tarceva® inhibits only EGFR kinase with high potency, although it can inhibit the signal transduction of other receptor kinases that probably heterodimerize with the EGFR. Nevertheless, other compounds that inhibit EGFR remain needed. [14] The serine-threonine kinase p70S6K is at the end of one pathway that controls cell growth and is frequently activated in many tumors, including uterine, adenocarcinoma, myeloma, and prostate cancers. Thus, it is desirable to identify compounds that inhibit p70S6K.

[15] BMX is a tyrosine kinase involved in interleukin-6 induced differentiation of prostate cancer cells. It plays a role in EGF-induced apoptosis of breast cancer cells, and is expressed in granocytes and myoloid leukemias, as well as other cancers. Thus, it is desirable to identify compounds that inhibit BMX.

[16] The serum and glucocorticoid-induced protein kinase ("SGK") is a downstream target in the PI3K/Akt pathway, believed to play a part in cancers such as breast and prostate cancer. Thus, it is desirable to identify compounds that inhibit SGK. [17] Ca2+/calmodulin-dependent protein kinase II ("CaMKII") indirectly modulates Fas-mediated signalling in glioma. Therefore inhibition of CaMK II may be effective in the treatment of glioma. See, Bao Feng Yang et al., J.Biological Chemistry, 278:7043-7050(2003). Thus, it is desirable to identify compounds that inhibit CaMKII. [18] Ret is a proto-oncogene implicated in many cancers such as thyroid cancer.

Thus, it is desirable to identify compounds that inhibit Ret.

[19] Endothelial-cell specific receptor protein tyrosine kinases such as KDR and

Tie-2 mediate the angiogenic process, and are thus involved in supporting the progression of cancers and other diseases involving inappropriate vascularization (e.g., diabetic retinopathy, choroidal neovascularization due to age-related macular degeneration, psoriasis, arthritis, retinopathy of prematurity, infantile hemangiomas). Thus, it is desirable to identify compounds that inhibit KDR.

[20] Ron (recepteur d'origine natais) is a receptor tyrosine kinase that is part of the MET proto-oncogene family. Inhibition of Ron has been shown to lead to a decrease in proliferation and induction of apoptosis. Thus, it is desirable to identify inhibitors of Ron. [21] IGF-IR (type 1 insulin-like growth factor receptor) perfoπns important roles in cell division, development, and metabolism, and in its activated state, plays a role in oncogenesis and suppression of apoptosis. IGF-IR is known to be overexpressed in a number of cancer cell lines (IGF-IR overexpression is linked to acromegaly and to cancer of the prostate). By contrast, down-regulation of IGF-IR expression has been shown to result in the inhibition of tumorigenesis and an increased apoptosis of tumor cells. Thus, it is desirable to identify compounds that inhibit IGF-IR.

[22] Some cancers develop resistance to certain kinase inhibitors over time and treatment. Resistance to a particular kinase inhibitor can be mediated by a loss of suppression of an enzyme at a branchpoint in the kinase pathway. The loss of suppression may lead to inappropriate activation of a parallel pathway from the original pathway. Thus, it is desirable to identify compounds that inhibit at least two kinases in order to provide compounds that are more efficacious than a very specific narrowly targeted compound that inhibits only one kinase. In particular, it is desirable to identify compounds that inhibit at least two of the AbI, Aurora-A, BIk, c-Raf, cSRC, Src, PRK2, FGFR3, FlO, Lck, Mekl, PDK-I, GSK30, EGFR, p70S6K, BMX, SGK, CaMKII, Tie-2, Ret, IGF-IR, Ron, and KDR kinases in animals, including humans, for the treatment and/or prevention of various diseases and conditions such as cancer.

[23] U.S. Patent No. 6,232,320, International Patent Publication Nos. WO

00/75145 and 99/62908 describes cell adhesion inhibiting antiinfammatory compounds. International Patent Publication No.03/080064 describes kinase inhibitors. U.S. Patent No. 6,713,474 describes pyrrolopyrimidines as therapeutic agents.

[24] U.S.PatentNo. 6,541,481 describes substituted bicyclic derivatives useful as anticancer agents.

[25] T. Peng et al., J. Chem. Inf. Comput. Sci.:43:298-303(2003) describes 3D-

QSAR and receptor modeling of tyrosine kinase inhyibitors with flexible atom receptor model (FLARM). International Patent Publication No. WO 98/43973 describes intermediate products and method for the production of pyrimidine derivatives. U.S. Patent No. 6,610,847, International Patent Publication Nos. WO 99/65908 and WO 99/65909 describe pyrrolo[2,3- djpyrimidine compounds. U.S. Patent No. 6,635,762 describes monocyclic-7H-pyrrolo[2,3- d]pyrimidine compounds. International Patent Publication No. WO 02/30944 describes fluorescent nuceobase conjugates having anionic linkers. International Patent Publication No. WO 04/009600 describes l-heterocyclyalkyl-S-sulfonylazaindole or azaindazole derivatives as 5-hydroxytryptamine-6 ligands. International Patent Publication No. WO04/007479 describes 3-guanidinocarbonyl-l-heteroaryl-indole derivatives. International Patent Publication No. WO 03/101990 describes l-(aminoalkyl)-3-sulfonylazaindoles as 5- hydroxytryptarnine-6 ligands.

[26] International Patent Publication No. WO 02/096909 describes optical resolution of (l-benzyl-4-niethylpiperidin-3-yl)-methylamine and the use thereof for the preparation of pyrrolo 2,3 -pyrimidine derivatives as protein kinase inhibitors. International Patent Publication No. WO02/50306 describes processes for determining the biological activity of epidermal growth factor receptor tyrosine kinase inhibitors. International Patent Publication No. WO02/41882 describes combination comprising an agent decreasing VEGF activity and an agent decreasing EGF activity.

[27] International Patent Publication No. WO 03/000187 describes novel pyrazolo- and pyrrolo-pyrimidines. International Patent Publication No. WO 02/057267, U.S. Patent Nos. 6,686,366, 6,680,324, and 6,673,802 describe compounds specific to adenosine Al, A2A, and A3 receptors. International Patent Publication No. WO 01/47507 describes combinations of a receptor tyrosine kinase inhibitor with an organic compound capable of binding to αl -acidic glycoprotein. International Patent Publication No. WO 04/013141 describes condensed pyridines and pyrimidines with TIE2 (TEK) activity. International Patent Publication No. WO 04/014850 describes substituted aminopyrimidines as neurokinin antagonists.

[28] International Patent Publication No. WO 03/000695 describes pyrrolopyrimidines as protein kinase inhibitors. U.S. Patent No. 6,187,778 describes 4- aminopyrrole (3,4-d) pyrimidines as neuropeptide Y receptor antagonists. U.S. Patent No. 6,140,317, 6,140,332, and 6,180,636 describe pyrrolopyrimidines. U.S. Patent Nos. 6,696,455, 6,537,999 and 5,877,178 describe pyrimidine derivatives. U.S. Patent No. 5,958,930 describes pyrrolo pyrimidine and furo pyrimidine derivatives. [29] International Patent Publication No. 03/000688 describes the preparation of azaindoles as protein kinase inhibitors. International Patent Publication Nos. WO 03/018021 and WO 03/018022 describe pyrimidines for treating IGF-IR related disorders, International Patent Publication No. WO 02/092599 describes pyrrolopyrimidines for the treatment of a disease that responds to an inhibition of the IGF-IR tyrosine kinase, International Patent Publication No. WO 01/72751 describes pyrrolopyrimidines as tyrosine kinase inhibitors. International Patent Publication No. WO 00/71129 describes pyrrolotriazine inhibitors of kinases. International Patent Publication No. WO 97/28161 describes pyrrolo[2,3- d]ρyrimidines and their use as tyrosine kinase inhibitors.

[30] Although the anticancer compounds described above have made a significant contribution to the art, there is a continuing need to improve anticancer pharmaceuticals with better selectivity or potency, reduced toxicity, or fewer side effects.

SUMMARY OF THE INVENTION

[31] Compounds represented by Formula (I):

(D or stereoisomers or pharmaceutically acceptable salts thereof, are inhibitors of least two of the AbI, Aurora-A, BIk, c-Raf, cSRC, Src, PRK2, FGFR3, Flt3, Lck, Mekl, PDK-I, GSK3/3, EGFR, p70S6K, BMX, SGK, CaMKII, Tie-2, Ret, Ron, IGF-IR, and KDR kinases in animals, including humans, for the treatment and/or prevention of various diseases and conditions such as cancer

DETAILED DESCRIPTION OF THE INVENTION [32] The present invention relates to compounds of Formula I:

(I) [33] or a pharmaceutically acceptable salt thereof, wherein

[34] X is N or C-CN;

.N— or ^

[36] Z is hetaryl,

-C₀-₆alkyl-(heterocyclyl), -C₀.₆alkyl-

(hetaryl), -C(O)-C₀.₆alkyl, -C(O)-C₀.₆alkyl-O-C₀.₆alkyl, -C(O)-C₀.₆alkyl-O-C_r.₆alkyl-O-C₀. ₆alkyl, -C(0)-C₀.₆alkyl-N(Co.₆alkyl)(Co.₆alkyl), -C(0)-Co.₆alkyl-(heterocyclyl), -C(O)-C₀. ₆alkyl-(heterocyclyl)-C(0)-Co.₆alkyl, -C(O)-C₀.₆alkyl- (hetaryl), -S(O)₂-C₀.₆alkyl, -S(O)₂- N(C_O-₆alkyl)(Co-₆alkyl), or -S(O)₂-(hetaryl), wherein any of the alkyl, heterocyclyl, or hetaryl optionally is substituted with 1-6 independent halo, OH, -Co-βalkyl-O-Co-ealkyl, -C₀.₆alkyl- N(Co.₆alkyl)(Co-₆alkyl), -C(0)-Co.₆alkyl-N(C₀.₆alkyl)(Co.₆alkyl), -C(0)-C₀.₆alkyl- (heterocyclyl), or -Co-βalkyl;

O

-N-C₂.₆alkyl-N O ^N — C₂._βalkyl-N N— C₀._βalkyl [37] or Z is ^{H V}-^V , ^^

N vj—- C₂.₆alkyl — N — Co.₆afkyl Co.₆alkyl

— N N— C₂._βalkyl— OH

C₂.₆alkyl — N— C_o.₆alkyj

C₀.₆alkyl

in which the wavy bond is the point of attachment, and wherein the piperazine or morpholine moieties are optionally substituted with 1-6 independent Co^alkyl groups;

[38] Y is -C(C_O-₆alkyl)(Co-₆alkyl)-, -N(C₀-₆alkyl)-, -N(C₀^alkyl)-C_I-6alkyl-, O, S,

>N-C₂.₆alkyl-N-(Co.₆alkyl)(Co.6alkyl), >N-C₂.₆alkyl-0-Co.6alkyl, >N-C₁^alkyl-C(0)-NH-Co.

₆alkyl, or >N-C₂.₆alkyl-N-C(O)-C,.₆alkyl; and

[39] Rl is aryl, hetaryl, or heterocyclyl, optionally substituted with. 1-6 independent halo, -CN, -OH, -Co-βalkyl, -Cs^ocycloalkyl, -haloCi.6alkyl, -C₂.₆alkynyl, -N(C_0- ₆a]kyl)(C₀._δalkyl), -C(0)-Co.₆alkyl-N(Co.₆alkyl)(C₀.₆alkyl), -C(O)-C₀.₆alkyl-(heterocyclyl), -C₁.

₆alkyl-C(0)-C₀.₆alkyl-N(Co-6alkyl)(C₀.₆alkyl),-0-C₀.₅alkyl-(heterocyclyl), -Co.₆alkyl-0-Co. βalkyl, -C_o.₆alkyl-N(Co.₆alkyl)(Co.₆alkyl), -O-C₀.₆alkyl-(hetaryl), -S(O)₂-N(C₀.₆alkyl)(C₀.

₆alkyl), aryl, hetaryl, or heterocyclyl substituents, or substituted with an oxo (=0) using a bond from the aryl, hetaryl, or heterocyclyl ring, wherein any of the substituents optionally is substituted with 1-6 independent halo, CN, OH, -C₀.₆alkyl-0-Co_₆alkyl, -C₀.₆alkyl-N(C₀.

₆alkyl)(C₀^alkyl), -C(O)-C₀.₆alkyl-N(C₀.₆alkyl)(C₀.₆alkyl), -C(O)-C₀.₆alkyl-(heterocyclyl), or

C_MalkyI.

[40] It is preferred that X is N.

/

[41] It is preferred that Cy is ^ — ^/ [42] It is preferred that Y is -N(C₀-₆alkyl)-. [43] Examples of Rl include, but are not limited to, the following groups, wherein the wavy bond is connected to Y:

[44] Examples of Z include, but are not limited to, the following groups, wherein the dotted line is connected to Cy:

[45] The molecular weight of the compounds of Formula (I) is preferably less than

800, more preferably less than 600.

[46] In the first aspect, the present invention is directed to a compound represented by Formula (I), or a stereoisomer, or a pharmaceutically acceptable salt thereof, wherein X is N and the other variables are as described above. [47] In an embodiment of the first aspect, the present invention is directed to a compound represented by Formula (I), or a stereoisomer, or a pharmaceutically acceptable

salt thereof, wherein X is N, Cy is -f —V- , and the other variables are as described above.

[48] In another embodiment of the first aspect, the present invention is directed to a compound represented by Formula (I), or a stereoisomer, or a pharmaceutically acceptable salt thereof, wherein X is N, Y is -N(C₀-₆alkyl)-, and the other variables are as described above.

[49] In a second aspect, the present invention is directed to a compound represented by:

or a stereoisomer, or a pharmaceutically acceptable salt thereof, wherein R2 is -Q-βalkyl, -C_2- ₆alkyl-N-(C_o.₆alkyl)(Co-salkyl), -Cwalkyl-O-Co-ealkyl, -Ci.₆alkyl-C(O)-NH-C₀-₆alkyl, or -C_2- ₆alkyl-N-C(O)-Ci._salkyl; and the other variables are as described above for Formula (I). [50] In an embodiment of the second aspect, the present invention is directed to a compound represented by:

or a stereoisomer, or a pharmaceutically acceptable salt thereof wherein is selected from the following table:

or a stereoisomer, or a pharmaceutically acceptable salt thereof.

[51] In a third aspect, the present invention is directed to a compound represented by:

or a stereoisomer, or a pharmaceut cally acceptable sa thereo<f, wherein R2 is -C₀.₆alkyl, -C₂. ₆alkyl-N-(C_o.₆alkyl)(Co.₆alkyl),

-C₁.₆alkyl-C(O)-NH-C₀.₆alkyl, or -C₂. ₆alkyl-N-C(O)-C₁.₆alkyl; and the other variables are as described above for Formula (I). [52] In an embodiment of the third aspect, the present invention is directed to a compound represented by:

wherein

is selected from the following table:

or a stereoisomer, or a pharmaceutically acceptable salt thereof.

[53] In a fourth aspect, the present invention is directed to a compound represented by Formula (I), or a stereoisomer, or a pharmaceutically acceptable salt thereof,

wherein Y-Rl is

or £ and the other variables are described above.

[54] In a fifth aspect, the present invention is directed to a compound represented by Formula (I), or a stereoisomer, or a pharmaceutically acceptable salt thereof, wherein X is C-CN and the other variables are as described above. [55] In an embodiment of the fifth aspect, the present invention is directed to a compound represented by Formula (I), or a stereoisomer, or a pharmaceutically acceptable

salt thereof, wherein X is C-CN, Cy is ^N — ' , and the other variables are as described above.

[56] In another embodiment of the fifth aspect, the present invention is directed to a compound represented by Formula (I), or a stereoisomer, or a pharmaceutically acceptable salt thereof, wherein X is C-CN, Y is -N(Co-₆alkyl)-, and the other variables are as described above.

[57] The compounds of the present invention include

027274

[58] While the prefeiτed groups for each variable have generally been listed above separately for each variable, preferred compounds of this invention include those in which several or each variable in Foπnula (I) is selected from the preferred, more preferred, most preferred, especially or particularly listed groups for each variable. Therefore, this invention is intended to include all combinations of preferred, more preferred, most preferred, especially and particularly listed groups.

[59] The compounds of the present invention include:

[60] 4-[4-(4-Fluoro-3-tiαiazol-5-ylphenylarnino)-7H-pyrrolo[2,3-(f]pyrirnidin-6- yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester;

[61] 4-[4-(4-Fluoro-3-miazol-5-ylphenylamino)-7H-pyrrolo[2,3-cT]pyrimidin-6- yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butylamide;

[62] 4-{4-[4-Fluoro-3-(lH-irmdazol-2-yl)-phenylamino]-7H-pyrrolo[2,3-d]- pyrirnidin-6-yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester;

[63] 4-{4-[4-Fluoro-3-(lH-Mdazol-2-yl)^henylamino]-7H-pyrrolo[2,3-d]- pyrirmdin-6-yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butylamide;

[64] 4-[4-(4-Fluoro-3-irnidazol-l-ylphenylarriino)-7H-pyrrolo[2,3-ύ(]pyrimidin-6- yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester;

[65] 4-[4-(4-Fluoro-3-irmdazol-l-ylphenylamino)-7H-pyrrolo[2,3--c(]pyrimidin-6- yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butylamide;

[66] 4-{4-[4-Fluoro-3-(4-methylpiperazin-l-yl)-phenylamino]-7H-pyrrolo[2,3-

J]pyrimidin-6-yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester;

[67] 4-{4-[4-Fluoro-3-(4-methylpiperazin-l-yl)-phenylamino]-7H-pyrrolo[2,3- d]pyrimidin-6-yl} -3 ,6-dihydro-2H-pyridine-l -carboxylic acid tert-butylamide;

[68] 4-{4-[4-Fluoro-3-(l-methylazetidin-3-ylmethyl)-phenylamino]-7H- pyrrolo[2,3-J]pyrimidin-6-yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester;

[69] 4- {4-[4-Fluoro-3 -(I -methylazetidin-3 -ylmethyl)-phenylamino] -7H- pyrrolo[2,3-d]pyrimidin-6-yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butylamide;

[70] 4-{4-[4-Fluoro-3-(l-methylazetidin-3-yloxy)-phenylamino]-7H-pyrrolo[2,3- rf]pyrimidin-6-yl} -3 ,6-dihydro-2H-pyridine-l -carboxylic acid tert-butyl ester;

[71] 4-{4-[4-Fluoro-3-(l-methylazetidin-3-yloxy)-phenylamino]-7H-pyrrolo[2,3- rf]pyrimidin-6-yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester;

[72] 4-{4-[4-Fluoro-3-(4-methylpiperazin-l-ylmethyl)-phenylamino]-7H- pyrrolo[2,3-</]pyrimidin-6-yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester;

[73] 4-{4-[4-Fluoro-3-(4-methylpiperazin-l-ylmethyl)-phenylamino]-7H- pyrrolo[2,3-d]pyrimidin-6-yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butylamide;

[74] 4-{4-[4-Fluoro-3-(l-methyl-l,2,3,6-tetrahydropyridin-4-yl)-phenylamino]-

7H-pyrrolo[2,3-cT|pyrimidin-6-yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester;

[75] 4-{4-[4-Fluoro-3-(l-methyl-l,2,3,6-tetrahydropyridin-4-yl)-phenylamino]-

7H-pyrrolo[2,3 -rf]pyrimidin-6-yl} -3 ,6-dihydro-2H-pyridine-l -carboxylic acid tert-butyl amide; [76] 4-{4-[4-Fluoro-3-(l-me%l-2,5-dihydro-lH-pyrrol-3-yl)-phenylamino]-7H- pyrrolo[2,3-(/lpyriinidiii-6-yl}-3,6-dihydro-2H-pyridiae-l-carboxylic acid tert-butyl ester;

[77] 4-{4-[4-Fluoro-3-(l-methyl-2,5-dihydro-lH-pyrrol-3-yl)-phenylamino]-7H- pyrrolo[2,3-J]pyrimidin-6-yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl amide;

[78] (5)-4- {4-[4-Fluoro-3 -(I -methylpyrrolidin-3 -yl)-phenylamino] -7H- pyrrolo[2,3-d]pyriinidin-6-yl}-3,6-diliydro-2H-pyridine-l-carboxylic acid tert-butyl ester;

[79] (S)-4-{4-[4-Fluoro-3-(l-metliylpyrrolidin-3-yl)-phenylamino]-7H- pyrrolo[2,3-J]pyrimidin-6-yl}-3,6-diliydro-2H-pyridine-l-carboxylic acid tert-butyl amide;

[80] (R)-4-{4-[4-Fluoro-3-(l-methylpyrrolidin-3-yl)-phenylamino]-7H- pyrrolo[2,3-(f]pyrimidin-6-yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester;

[81] (i?)-4-{4-[4-Fluoro-3-(l-methylpyrrolidin-3-yl)-phenylamino]-7H- pyrrolo[2,3-d]pyrimidin-6-yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl amide;

[82] {4-[4-(BenzoMazol-6-ylamino)-7H-pyrrolo[2,3-J]pyrirnidin-6-yl]-3,6-- diliydro-2H-pyridin-l-yl}-(2,2,4-trimethylpiperazin-l-yl)-methanone;

[83] {4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-d]pyrimidin-6-yl]-3,6- dihydro-2H-pyridin-l-yl}-(2,4,5-trimethylpiperazin-l-yl)-methanone;

[84] {4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-J]pyrimidin-6-yl]-3,6- dihydro-2H-pyridin-l-yl}-(3,4,5-trimethylpiperazm-l-yl)-methanone;

[85] {4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-J]pyrirnidin-6-yl]-3,6- dihydro-2H-pyridin-l-yl}-[4-(2,2,2-trifluoroethyl)-piperazin-l-yl]-methanone;

[86] {4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-J]pyrimidin-6-yl]-3,6- dib.ydro-2H-pyridin-l-yl}-(4-tert-butylpiperazin-l-yl)-methanone;

[87] Benzothiazol-6-yl-[6-(3 ,6-dihydro-2H-[ 1 ,2']bipyridinyl-4-yl)-7H-pyrrolo[2,3 -

J]pyrimidin-4-yl] -amine;

[88] Benzothiazol-6-yl-[6-(l-thiazol-2-yl-l,2₃3,6-tetrahydropyridin-4-yl)-7H- pyrrolo[2,3-d]pyrimidin-4-yl]-amine;

[89] Benzothiazol-6-yl-[6-(l-oxazol-2-yl-l,2,3,6-tetrahydropyridin-4-yl)-7H- pyrrolo[2,3 -d]pyi"imidin-4-yl] -amine;

[90] 4-[4-(3-Phenyl-3H-benzimidazol-5-ylamino)-7H-pyrrolo[2,3-cf]pyrimidin-6- yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester;

[91] 4-[4-(3-Phenyl-3H-benzimidazol-5-ylamino)-7H-pyrrolo[2,3-d]pyrimidin-6- yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butylamide;

[92] 4-{4-[3-(2-Carbamoylphenyl)-3H-benzimidazol-5-ylamino]-7H-pyrrolo[2,3- d]pyrimidin-6-yl} -3 ,6-dihydro-2H-pyridine-l -carboxylic acid tert-butylamide;

[93] 4-{4-[3-(2-Carbamoylphenyl)-3H-benzimidazol-5-ylamino]-7H-pyrrolo[2,3- d]pyrimidin-6-yl} -3 ,6-dihydro-2H-pyridine-l -carboxylic acid tert-butyl ester; [94] 4-{4-[3-(2-Aminoe1hyl)-3H-benziinidazol-5-ylai]χιno]-7H-pyrrolo[2,3-

J]pyrimidin-6-yl} -3 ,6-dihydro-2H-pyridine-l -carboxylic acid tert-butylamide; • [95] 4-{4-[3<2-Ainmoe%l)-3H-ben2imidazol-5-ylainino]-7H-pyrrolo[2,3-

<i]pyrimidin-6-yl} -3 ,6-dihydro-2H-pyridine-l -carboxylic acid tert-butyl ester; [96] 4- {4-[3 -(2-Dimethylaminoethyl)-3H-benzimidazol-5 -ylamino] -7H- pyrrolo[2,3 -d]pyrimidin-6-yl} -3 ,6-dihydro-2H-pyridine-l -carboxylic acid tert-butylamide; [97] 4-{4-[3-(2-Dimetiiylaminoethyl)-3H-benzimidazol-5-ylamino]-7H- pyrrolo[2,3-d^f]pyrimidin-6-yl}-3,6-dih.ydro-2H-pyridine-l-carboxylic acid tert-butyl ester; [98] 4-{443<2-Acetylarninoethyl)-3H-benzimidazol-5-ylamino]-7H-ρyrrolo[2,3- rf]pyrimidin-6-yl} -3 ,6-dihydro-2H-pyridine-l -carboxylic acid /ert-butylamide; [99] 4-{4-[3-(2-Acetylaimnoe%l)-3H-benzinτidazol-5-ylamino]-7H-pyrrolo[2,3-

J]pyrimidiri-6-yl} -3 ,6-dihydro-2H-pyridine-l -carboxylic acid tert-butyl ester; [100] 4-[4-(Imidazo[l,2-α]pyridin-6-ylarnino)-7H-pyrrolo[2,3-cr]pyrimidin-6-yl]-

3,6-dihydro-2H-pyridine-l -carboxylic acid tert-butylamide;

[101] 4-[4-(Imidazo[l,2-α]pyridin-6-ylamino)-7H-pyrrolo[2,3-rf]pyrimidiri-6-yl]-

3, 6-dihydro-2H-pyridine-l -carboxylic acid

ester;

[102] 4-[4-(3-Methylimidazo[l,2-α]pyridin-6-ylarnino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid /ert-butylamide; [103] 4-[4-(3-Me%limidazo[l,2-fl]pyridin-6-ylarriino)-7H-pyrrolo[2_s3-d]- pyrimidin-6-yl]-3,6-diliydro-2H-pyridine-l-carboxylic acid tert-butyl ester; [104] 4-[4-(3-Phenyliimdazo[l,2-α]pyridin-6-ylaimno)-7H-pyrrolo[2,3-J]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butylamide; [105] 4-[4-(3-Phenylimidazo[l ,2-«]pyridin-6-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-diliydro-2H-pyridine-l -carboxylic acid tert-butyl ester; [106] 4-{4-[3-(2-Carbamoylphenyl)-imidazo[l,2-α]pyridin-6-ylamino]-7H- pyrrolo[2,3-c(]pyrimidin-6-yl}-3,6-dih.ydro-2H-pyridine-l-carboxylic acid tert-butylamide; [107] 4- {4-[3-(2-Carbamoylphenyl)-imidazo[l ,2-α]pyridin-6-ylamino]-7H- pyrrolo[2,3-d]pyrimidin-6-yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester; [108] 4-{4-[3-(2-Dime%larninoethyl)-irnidazo[l,2-α]pyridin-6-ylamino]-7H- pyrrolo[2,3-cT|pyrimidin-6-yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butylamide; [109] 4-{4-[3-(2-Dimethylaminoethyl)-imidazo[l,2-α]pyridin-6-ylamino]-7H- pyrrolo[2,3-rf]pyrimidin-6-yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester; [110] 4-{4-[3-(2-Acetylaminoethyl)-imidazo[l,2-α]pyridin-6-ylaimno]-7H- pyrrolo[2,3-d]pyrimidin-6-yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butylamide; [111] 4-{4-[3-(2-Acetylaminoethyl)-imidazo[l,2-α]pyridin-6-ylamino]-7H- pyrrolo[2,3-rf]pyrimidin-6-yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester; [112] 4-[4-(3-Dimethylairdnomethylimidazo[l,2-α]pyridin-6-ylamino)-7H- pyrrolo[2,3-rf]pyrimidin-6-yl]-3,6-diliydro-2H-pyridine-l-carboxylic acid tert-butylamide;

[113] 4-[4-(3-Dimethylarαinomethyliinidazo[l,2-α]pyridin-6-ylamino)-7H- pyrrolo[2,3-rf]pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester;

[114] 4-[4-(7-Aimnome1iiyl-li7-indazol-5-ylaimno)-7H-pyrrolo[2,3-rf]pyrimidin-6- yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butylamide;

[115] 4-[4-(7-Aπύnome&yl-lH4ndazol-5-ylamino)-7H-pyrrolo[2,3-6r]pyrimidin-6- yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester;

[116] 4-[4-(7-Anτinome%l-l-me%l-lH-indazol-5-ylaiiiino)-7H-pyrrolo[2,3- d]ρyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l -carboxylic acid tert-butylamide;

[117] 4-[4-(7-Aininome%l-l-me1hyl-lH-inda2»l-5-ylainino)-7H-pyrrolo[2,3- rf]pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester;

[118] 4-[4-(7-Dimethylaminomethyl-l -methyl-lH-indazol-5-ylamino)-7H- pyrrolo[2,3-rf]pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butylamide;

[119] 4-[4-(7-Dimethylaminomethyl-l-methyl4H-indazol-5-ylamino)-7H- pyrrolo[2,3-c(]pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid /er/-butyl ester;

[120] 4^4-(7-Dimethylaminomethyl-lH-indazol-5-ylamino)-7H-pyrrolo[2,3- rf]pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butylamide;

[121] 4-[4-(7-Dimethylarninometb.yl-lH-indazol-5-ylamino)-7H-pyrrolo[2,3- rf]pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester;

[122] 4-{447-(2-Dime%laminoethyl)-lH-indazol-5-ylamino]-7H-pyrrolo[2,3- rf]pyrimidin-6-yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butylamide;

[123] 4-{4^7<2-Dime%larninoethyl)-lH-iridazol-5-ylarriino]-7H-pyrrolo[2,3- cdpyrimidin-6-yl} -3 ,6-dihydro-2H-pyridine-l -carboxylic acid tert-bntyl ester;

[124] 4-{4-[7-(2-Dime%laminoethyl)-l-methyl-lH-indazol-5-ylamino]-7H- pyrrolo[2,3-rf]pyrimidin-6-yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid to^-butylamide;

[125] 4-{4-[7-(2-Dime%laininoe%l)-l-me1iiyl-lH-mdazol-5-ylarnino]-7H- pyrrolo[2,3-d]pyrimidin-6-yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-buty\ ester;

[126] 4-[4-(Imidazo[l,5-α]pyridin-6-ylamino)-7H-pyrrolo[2,3-^pyrimidin-6-yl]-

3, 6-dihydro-2H-pyridine-l -carboxylic acid tert-butylamide;

[127] 4-[4-(Imidazo[l,5-α]pyridin-6-ylarnino)-7H-pyrrolo[2,3-(/lpyrimidin-6-yl]-

3, 6-dihydro-2H-pyridine-l -carboxylic acid ter/-butyl ester;

[128] 4-[4-(3-Methylimidazo[l,5-fl]pyridin-6-ylamino)-7H-pyrrolo[2,3-<f]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butylamide;

[129] 4-[4-(3-Methylirnidazo[l,5-α]pyridin-6-ylamino)-7H-pyrrolo[2,3-d]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-buty\ ester; [130] 4-[4-(l-Methylimidazo[l,5-α]pyridin-6-ylamino)-7H-ρyrrolo[2,3-d]- pyrimidin-β-yy-S.ό-dihydro^H-pyridine-l-carboxylic acid tert-butylaniide;

[131] 4-[4-(l-Methylimidazo[l,5-α]pyridin-6-ylamino)-7/-^'-pyrrolo[2,3-d]- pyriirridin-6-yl]-3,6-dihydro-2H-pyridine-l -carboxylic acid tert-butyl ester;

[132] 4-[4<IiΩidazo[l,5-α]pyridin-7-ylamino)-7H-pyrrolo[2,3-^pyrimidin-6-yl]-

3 ,6-dihydro-2H-pyridine-l -carboxylic acid ter/-butylamide;

[133] 444-(Imidazo[l,5-α]pyridin-7-ylamino)-7H-pyrrolo[2,3-J]pyrimidin-6-yl]-

3 ,6-dihydro-2H-pyridine-l -carboxylic acid tert-butyl ester;

[134] 4-[4-(3-Methylimidazo[l ,5-α]pyridin-7-ylamino)-7H-pyrrolo[2,3-<f]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butylamide;

[135] 4-[4<3-Me%limida2»[l₅5-β]pyridin-7-ylamino)-7H-pyrrolo[2,3-d]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester;

[136] 4^4<l-Methylirnidazo[l,5-a]pyridin-7-ylarnino)-7H-pyrrolo[2,3-J]- pyrimidin-ό-yy-S^-dihydro^H-pyridine-l-carboxylic acid tert-butylamide;

[137] 4-[4-(l-Methylimidazo[l,5-a]pyridin-7-ylamino)-7H-pyrrolo[2,3-(fl- pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester;

[138] 444-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-rf]pyrimidin-6-yl]-3,6- dihydro-2H-pyridine-l-carboxylic acid (2-hydroxy-l,l-dimethylethyl)-amide;

[139] 4-[4-(l-Me%l-lH-indazol-5-ylamino)-7H-pyrrolo[2,3-d]pyrimidin-6-yl]-

3 ,6-dihydro-2H-pyridine-l -carboxylic acid (2-hydroxy-l , 1 -dimethylethyl)-amide;

[140] 4-[4-(Benzothiazol-6-ylarnino)-7H-pyrrolo[2,3-cr]pyrirnidin-6-yl]-3,6- dihydro-2H-pyridine-l -carboxylic acid (2-methoxy-l ,1 -dimethylethyl)-amide;

[141] 4-[4-(l-Me%l-lH-indazol-5-ylamino)-7H-pyrrolo[2,3-d']pyrimidin-6-yl]-

3 ,6-dihydro-2H-pyridine-l -carboxylic acid (2-methoxy-l , 1 -dimethylethyl)-amide;

[142] 4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-rf]pyrimidin-6-yl]-3,6- dihydro-2H-pyridine-l -carboxylic acid (2-dimethylamino-l,l-dimethylethyl)-amide;

[143] 4-[4-(l-Methyl-lH-indazol-5-ylamino)-7H-pyrrolo[2,3-cTlpyriiiiidin-6-yl]-

3, 6-dihydro-2H-pyridine-l -carboxylic acid (2-dimethylamino-l,l-dimethylethyl)-amide;

[144] 4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-rf]pyrimidin-6-yl]-3,6- dihydro-2ϋT-pyridine-l -carboxylic acid (l,l-dimethyl-2-pyrrolidin-l-ylethyl)-amide;

[145] 4-[4-(l-Methyl-lH-indazol-5-ylamino)-7H-pyrrolo[2,3-rf]pyrimidin-6-yl]-

3 ,6-dihydro-2H-pyridine-l -carboxylic acid (1 ,1 -dimethyl-2-pyrrolidin-l -ylethyl)-amide;

[146] 4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-d]pyrimidin-6-yl]-3,6- dihydro-2H-pyridine-l-carboxylic acid (l,l-dimethyl-2-moφholin-4-ylethyl)-amide;

[147] 4-[4-(l-Methyl-lH-indazol-5-ylamino)-7H-pyrrolo[2,3-rf]pyrimidin-6-yl]-

3 ,6-dihydro-2H-pyridine-l -carboxylic acid (1 ,1 -dimethyl-2-moφholin-4-ylethyl)-amide; [148] 444-(lH-Indol-5-yIamino)-7H-pyrrolo[2,3-φyrimidm-6-yl]-3,6-dihydro-

2H-pyridine-l-carboxylic acid tert-butylamide;

[149] 4-[4-(Quinolin-6-ylamino)-7H-pyrrolo[2,3-rf]pyrimidin-6-yl]-3,6-dihydro-

2H-pyridine-l-carboxylic acid fert-butylamide;

[150] (Ηexahydropyrrolo [ 1 ,2-α]pyrazin-2-yl)- {4-[4-(imidazo [ 1 ,2-<z]pyridin-6- ylamino)-7H-pyrrolo[2,3 -ύf]pyrimidin-6-yl]-3 ,6-dihydro-2H-pyridin-l -yl} -methanone;

[151] (Ηexahydropyrrolo[l,2-α]pyrazin-2-yl)-{4-[4-(3-methyl-3H-benzoimidazol-

5-ylaπύno)-7H-pyrrolo[2,3-d]pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yl}-methanone;

[152] (Ηexahydropyrrolo[ 1 ,2-α]pyrazin-2 -yl)- {4-[4-( 1 -methyl- lH-indazol-5 - ylamino)-7H-pyrrolo[2,3-fi(]pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yl}-methanone;

[153] {4-[4-(Benzoώiazol-6-ylamino)-7H-pyrrolo[2,3-rf]pyrimidin-6-yl]-3₎6- dihydro-2H-pyridin-l-yl}-(hexahydropyrrolo[l,2-α]pyrazin-2-yl)-methanone.

[154] As used herein, unless stated otherwise, "alkyl" as well as other groups having the prefix "alk" such as, for example, alkoxy, alkanyl, alkenyl, alkynyl, and the like, means carbon chains which may be linear or branched or combinations thereof. Examples of alkyl groups include methyl, ethyl, propyl, isopropyl, butyl, sec- and tert-butyl, pentyl, hexyl, heptyl and the like. "Alkenyl", "alkynyl" and other like terms include carbon chains having at least one unsaturated carbon-carbon bond.

[155] As used herein, for example, "Co^alkyl" is used to mean an alkyl having 0-4 carbons - that is, 0, 1 , 2, 3, or 4 carbons in a straight or branched configuration. An alkyl having no carbon is hydrogen when the alkyl is a terminal group. An alkyl having no carbon is a direct bond when the alkyl is a bridging (connecting) group.

[156] As used herein, the ">" symbol in front of a nitrogen atom refers to two bonds not to the same atom (not a double bond to the nitrogen).

[157] The terms "cycloalkyl" and "carbocyclic ring" mean carbocycles containing no heteroatoms, and include mono-, bi-, and tricyclic saturated carbocycles, as well as fused and bridged systems. Such fused ring systems can include one ring that is partially or fully unsaturated, such as a benzene ring, to form fused ring systems, such as benzofused carbocycles. Cycloalkyl includes such fused ring systems as spirofused ring systems.

Examples of cycloalkyl and carbocyclic rings include C3-10cycloalkyl groups, particularly

C3 -8 cycloalkyl groups, such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, and decahydronaphthalene, adamantane, indanyl, 1,2,3,4-tetrahydronaphthalene and the like.

[158] The term "halogen" includes fluorine, chlorine, bromine, and iodine atoms.

[159] The term "carbamoyl" unless specifically described otherwise means -C(O)-

NH- or -NH-C(O)-.

[160] The term "aryl" is well known to chemists. The preferred aryl groups are phenyl and naphthyl, more preferably phenyl. [161] The term "hetaryl" is well known to chemists. The term includes 5- or 6- membered heteroaryl rings containing 1-4 heteroatoms chosen from oxygen, sulfur, and nitrogen in which oxygen and sulfur are not next to each other. Examples of such heteroaryl rings are furyl, thienyl, pyrrolyl, pyrazolyl, imidazolyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, triazolyl, oxadiazolyl, thiadiazolyl, tetrazolyl, pyridyl, pyridazinyl, pyrimidinyl, pyrazinyl, and triazinyl. The term "hetaryl" includes hetaryl rings with fused carbocyclic ring systems that are partially or fully unsaturated, such as a benzene ring, to form a benzofused hetaryl. For example, benzimidazole, benzoxazole, benzothiazole, benzofuran, quinoline, isoquinoline, quinoxaline, and the like. The term "hetaryl" also includes fused 5-6, 5-5, 6-6 ring systems, optionally possessing one nitrogen atom at a ring junction. Examples of such hetaryl rings include, but are not limited to, pyrrolopyrimidinyl, imidazo[l,2-α]pyridinyl, imidazo[2,l-&]thiazolyl, imidazo[4,5-δ]pyridine, pyrrolo[2,l-/l[l,2,4]triazinyl, and the like. Hetaryl groups may be attached to other groups through their carbon atoms or the heteroatom(s), if applicable. For example, pyrrole may be connected at the nitrogen atom or at any of the carbon atoms.

[162] Unless otherwise stated, the terms "heterocyclic ring", "heterocyclyl" and

"heterocycle" are equivalent, and include 4—10-membered, e.g. 5-membered, saturated or partially saturated rings containing 1-4 heteroatoms chosen from oxygen, sulfur, and nitrogen. The sulfur and oxygen heteroatoms are not directly attached to one another. Any nitrogen heteroatoms in the ring may optionally be substituted with C^alkyl. Examples of heterocyclic rings include azetidine, oxetane, tetrahydrofuran, tetrahydropyran, oxepane, oxocane, thietane, thiazolidine, oxazolidine, oxazetidine, pyrazolidine, isoxazolidine, isothiazolidine, tetrahydrothiophene, tetrahydrothiopyran, thiepane, thiocane, azetidine, pyrrolidine, piperidine, N-methylpiperidine, azepane, 1,4-diazapane, azocane, [l,3]dioxane, oxazolidine, piperazine, homopiperazine, morpholine, thiomorpholine, 1,2,3,6- tetrahydropyridine and the like. Other examples of heterocyclic rings include the oxidized forms of the sulfur-containing rings. Thus, tetrahydrothiophene- 1 -oxide, tetrahydrothiophene- 1 , 1 -dioxide, thiomorpholine-1 -oxide, thiomorpholine- 1 , 1 -dioxide, tetrahydrothiopyran-1 -oxide, tetrahydrothiopyran-1, 1-dioxide, thiazolidine- 1 -oxide, and thiazolidine-1,1 -dioxide are also considered to be heterocyclic rings. The term "heterocyclic" also includes fused ring systems and can include a carbocyclic ring that is partially or fully unsaturated, such as a benzene ring, to form benzofused heterocycles. For example, 3,4- dihydro-l,4-benzodioxine, tetrahydroquinoline, tetrahydroisoquinoline and the like. [163] Compounds described herein may contain one or more asymmetric centers and may thus give rise to diastereomers and optical isomers. The present invention includes all such possible diastereomers as well as their racemic mixtures, their substantially pure resolved enantiomers, all possible geometric isomers, and pharmaceutically acceptable salts thereof. The above Formula (I) is shown without a definitive stereochemistry at certain positions. The present invention includes all stereoisomers of Formula (I) and pharmaceutically acceptable salts thereof. Further, mixtures of stereoisomers as well as isolated specific stereoisomers are also included. During the course of the synthetic procedures used to prepare such compounds, or in using racemization or epimerization procedures known to those skilled in the art, the products of such procedures can be a mixture of stereoisomers.

[164] When a tautomer of the compound of Formula (I) exists, the present invention includes any possible tautomers and pharmaceutically acceptable salts thereof, and mixtures thereof, except where specifically stated otherwise.

[165] When the compound of Formula (I) and pharmaceutically acceptable salts thereof exist in the form of solvates or polymorphic forms, the present invention includes any possible solvates and polymorphic forms. A type of a solvent that forms the solvate is not particularly limited so long as the solvent is pharmacologically acceptable. For example, water, ethanol, propanol, acetone or the like can be used.

[166] The invention also encompasses a pharmaceutical composition that is comprised of a compound of Formula (I), or a pharmaceutically acceptable salt thereof, in combination with a pharmaceutically acceptable carrier.

[167] Preferably the composition is comprised of a pharmaceutically acceptable carrier and a non-toxic therapeutically effective amount of a compound of Formula (I), or a pharmaceutically acceptable salt thereof.

[168] Moreover, within this preferred embodiment, the invention encompasses a pharmaceutical composition for the treatment of disease by inhibiting glycogen phosphorylase, resulting in the prophylactic or therapeutic treatment of diabetes, hyperglycemia, hypercholesterolemia, hyperinsulinemia, hyperlipidemia, hypertension, atherosclerosis or tissue ischemia e.g. myocardial ischemia comprising a pharmaceutically acceptable carrier and a non-toxic therapeutically effective amount of compound of Formula (I), or a pharmaceutically acceptable salt thereof.

[169] The term "pharmaceutically acceptable salts" refers to salts prepared from pharmaceutically acceptable non-toxic bases or acids. When the compound of the present invention is acidic, its corresponding salt can be conveniently prepared from pharmaceutically acceptable non-toxic bases, including inorganic bases and organic bases. Salts derived from such inorganic bases include aluminum, ammonium, calcium, copper (ic and ous), ferric, ferrous, lithium, magnesium, potassium, sodium, zinc and the like salts. Particularly preferred are the ammonium, calcium, magnesium, potassium and sodium salts. Salts derived from pharmaceutically acceptable organic non-toxic bases include salts of primary, secondary, and tertiary amines, as well as cyclic amines and substituted amines such as naturally occurring and synthesized substituted amines. Other pharmaceutically acceptable organic non-toxic bases from which salts can be formed include arginine, betaine, caffeine, choline, N'N'-dibenzylethylenediamine, diethylamine, 2-diethylaminoethanol, 2- dimethylaminoethanol, ethanolamine, ethylenediamine, N-ethylmoφholine, N- ethylpiperidine, glucamine, glucosamine, histidine, hydrabamine, isopropylamine, lysine, methylglucamine, morpholine, piperazine, piperidine, polyamine resins, procaine, purines, theobromine, triethylamine, trimethylamine, tripropylamine, tromethamine and the like. [170] When the compound of the present invention is basic, its corresponding salt can be conveniently prepared from pharmaceutically acceptable non-toxic acids, including inorganic and organic acids. Such acids include, for example, acetic, benzenesulfonic, benzoic, camphorsulfonic, citric, ethanesulfonic, fumaric, gluconic, glutamic, hydrobromic, hydrochloric, isethionic, lactic, maleic, malic, mandelic, methanesulfonic, mucic, nitric, pamoic, pantothenic, phosphoric, succinic, sulfuric, tartaric, p-toluenesulfonic acid and the like. Particularly preferred are citric, hydrobromic, hydrochloric, maleic, phosphoric, sulfuric, and tartaric acids.

[171] Since the compounds of Formula (I) are intended for pharmaceutical use they are preferably provided in substantially pure form, for example at least 60% pure, more suitably at least 75% pure especially at least 98% pure (% are on a weight for weight basis). [172] The pharmaceutical compositions of the present invention comprise a compound represented by Formula (I), or a pharmaceutically acceptable salt thereof, as an active ingredient, a pharmaceutically acceptable carrier and optionally other therapeutic ingredients or adjuvants. The compositions include those suitable for oral, rectal, topical, and parenteral (including subcutaneous, intramuscular, and intravenous) administration, although the most suitable route in any given case will depend on the particular host, and nature and severity of the conditions for which the active ingredient is being administered. The compositions are preferably suitable for oral administration. The pharmaceutical compositions may be conveniently presented in unit dosage form and prepared by any of the methods well known in the art of pharmacy.

[173] In practice, the compounds of Formula (I), or pharmaceutically acceptable salts thereof, can be combined as the active ingredient in intimate admixture with a pharmaceutical carrier according to conventional pharmaceutical compounding techniques. The carrier may take a wide variety of forms depending on the form of preparation desired for administration, e.g. oral or parenteral (including intravenous). Thus, the pharmaceutical compositions of the present invention can be presented as discrete units suitable for oral administration such as capsules, sachets or tablets each containing a predetermined amount of the active ingredient. Further, the compositions can be presented as a powder, as granules, as a solution, as a suspension in an aqueous liquid, as a non-aqueous liquid, as an oil-in-water emulsion, or as a water-in-oil liquid emulsion. In addition to the common dosage forms set out above, the compounds of Formula (I), or pharmaceutically acceptable salts thereof, may also be administered by controlled release means and/or delivery devices. The compositions may be prepared by any of the methods of pharmacy. In general, such methods include a step of bringing into association the active ingredient with the carrier that constitutes one or more necessary ingredients. In general, the compositions are prepared by uniformly and intimately admixing the active ingredient with liquid carriers or finely divided solid carriers or both. The product can then be conveniently shaped into the desired presentation. [174] Thus, the pharmaceutical compositions of this invention may include a pharmaceutically acceptable carrier and a compound of Formula (I) or a pharmaceutically acceptable salt thereof. The compounds of Fonnula (I), or pharmaceutically acceptable salts thereof, can also be included in pharmaceutical compositions in combination with one or more other therapeutically active compounds.

[175] The pharmaceutical carrier employed can be, for example, a solid, liquid, or gas. Examples of solid carriers include lactose, terra alba, sucrose, talc, gelatin, agar, pectin, acacia, magnesium stearate, and stearic acid. Examples of liquid carriers are sugar syrup, peanut oil, olive oil, and water. Examples of gaseous carriers include carbon dioxide and nitrogen.

[176] In preparing the compositions for oral dosage form, any convenient pharmaceutical media may be employed. For example, water, glycols, oils, alcohols, flavoring agents, preservatives, coloring agents, and the like may be used to form oral liquid preparations such as suspensions, elixirs and solutions; while carriers such as starches, sugars, microcrystalline cellulose, diluents, granulating agents, lubricants, binders, disintegrating agents, and the like may be used to form oral solid preparations such as powders, capsules and tablets. Because of their ease of administration, tablets and capsules are the preferred oral dosage units whereby solid pharmaceutical carriers are employed. Optionally, tablets may be coated by standard aqueous or nonaqueous techniques.

[177] A tablet containing the composition of this invention may be prepared by compression or molding, optionally with one or more accessory ingredients or adjuvants. Compressed tablets may be prepared by compressing, in a suitable machine, the active ingredient in a free-flowing form such as powder or granules, optionally mixed with a binder, lubricant, inert diluent, surface active or dispersing agent. Molded tablets may be made by molding in a suitable machine, a mixture of the powdered compound moistened with an inert liquid diluent. Each tablet preferably contains from about 0.05mg to about 5g of the active ingredient and each sachet or capsule preferably contains from about 0.05mg to about 5g of the active ingredient. [178] For example, a formulation intended for oral administration to humans may contain from about 0.5mg to about 5g of active agent, compounded with an appropriate and convenient amount of carrier material, which may vary from about 5 to about 95% of the total composition. Unit dosage forms will generally contain from about lmg to about 2g of the active ingredient, typically 25mg, 50mg, lOOmg, 200mg, 300mg, 400mg, 500mg, 600mg, 800mg, or lOOOmg.

[179] Pharmaceutical compositions of the present invention suitable for parenteral administration may be prepared as solutions or suspensions of the active compounds in water. A suitable surfactant can be included such as, for example, hydroxypropylcellulose. Dispersions can also be prepared in glycerol, liquid polyethylene glycols, and mixtures thereof in oils. Further, a preservative can be included to prevent the detrimental growth of microorganisms.

[180] Pharmaceutical compositions of the present invention suitable for injectable use include sterile aqueous solutions or dispersions. Furthermore, the compositions can be in the form of sterile powders for the extemporaneous preparation of such sterile injectable solutions or dispersions. In all cases, the final injectable form must be sterile and must be effectively fluid for easy syringability. The pharmaceutical compositions must be stable under the conditions of manufacture and storage; thus, preferably should be preserved against the contaminating action of microorganisms such as bacteria and fungi. The carrier can be a solvent or dispersion medium containing, for example, water, ethanol, polyol (e.g. glycerol, propylene glycol and liquid polyethylene glycol), vegetable oils, and suitable mixtures thereof.

[181] Pharmaceutical compositions of the present invention can be in a form suitable for topical use such as, for example, an aerosol, cream, ointment, lotion, dusting powder, or the like. Further, the compositions can be in a form suitable for use in transdermal devices. These formulations may be prepared, utilizing a compound of Formula (I), or a pharmaceutically acceptable salt thereof, via conventional processing methods. As an example, a cream or ointment is prepared by admixing hydrophilic material and water, together with about 5wt% to about 10wt% of the compound, to produce a cream or ointment having a desired consistency.

[182] Pharmaceutical compositions of this invention can be in a form suitable for rectal administration wherein the carrier is a solid. It is preferable that the mixture forms unit dose suppositories. Suitable carriers include cocoa butter and other materials commonly used in the art. The suppositories may be conveniently formed by first admixing the composition with the softened or melted carrier(s) followed by chilling and shaping in molds. [183] In addition to the aforementioned carrier ingredients, the pharmaceutical formulations described above may include, as appropriate, one or more additional carrier ingredients such as diluents, buffers, flavoring agents, binders, surface-active agents, thickeners, lubricants, preservatives (including anti-oxidants) and the like. Furthermore, other adjuvants can be included to render the formulation isotonic with the blood of the intended recipient. Compositions containing a compound of Formula (I), or a pharmaceutically acceptable salt thereof, may also be prepared in powder or liquid concentrate form. [184] Generally, dosage levels on the order of 0.01mg/kg to about 150mg/kg of body weight per day are useful in the treatment of the above-indicated conditions, or alternatively about 0.5mg to about 7g per patient per day. For example, lung cancer may be effectively treated by the administration of from about 0.01 to 50mg of the compound per kilogram of body weight per day, or alternatively about 0.5mg to about 3.5g per patient per day. Similarly, breast cancer may be effectively treated by the administration of from about 0.01 to 50mg of the compound per kilogram of body weight per day, or alternatively about 0.5mg to about 3.5g per patient per day.

[185] It is understood, however, that the specific dose level for any particular patient will depend upon a variety of factors including the age, body weight, general health, sex, diet, time of administration, route of administration, rate of excretion, drug combination and the severity of the particular disease undergoing therapy.

[186] The compounds of Formula (I) and pharmaceutically acceptable salts thereof, may be used in the treatment of diseases or conditions in which the AbI, Aurora- A, BIk, c- Raf, cSRC, Src, PRK2, FGFR3, Flt3, Lck, Mekl, PDK-I, GSK3/3, EGFR, p70S6K, BMX, SGK, CaMKII, Tie-2, Ret, Ron, IGF-IR, or KDR kinases plays a role. [187] Thus the invention also provides a method for the treatment of a disease or condition in which the AbI, Aurora-A, BIk, c-Raf, cSRC, Src, PRK2, FGFR3, Flt3, Lck, Mekl, PDK-I, GSK3j8, EGFR, p70S6K, BMX, SGK, CaMKII, Tie-2, Ret, Ron, IGF-IR, or KDR kinases plays a role comprising a step of administering to a subject in need thereof an effective amount of a compound of Formula (I), or a pharmaceutically acceptable salt thereof. [188] Diseases or conditions in which the AbI, Aurora-A, BIk, c-Raf, cSRC, Src,

PRK2, FGFR3, Flt3, Lck, Mekl, PDK-I, GSK3/3, EGFR, p70S6K, BMX, SGK, CaMKII, Tie-2, Ret, Ron, IGF-IR, or KDR kinases plays a role include lung, breast, prostate, pancreatic, head and neck cancers, as well as leukemia.

[189] The invention also provides a method for the treatment of cancers of the lung, breast, prostate, pancreas, head, neck or blood comprising a step of administering to a subject in need thereof an effective amount of a compound of Formula (I), or a pharmaceutically acceptable salt thereof.

[190] The invention also provides a method for the treatment of lung cancer, breast cancer, prostate cancer, pancreatic cancer, head cancer, neck cancer, or leukemia in a human demonstrating such cancers comprising a step of administering to a subject in need thereof an effective amount of a compound of Foπnula (I), or a pharmaceutically acceptable salt thereof.

[191] The invention also provides a method for the treatment of cancers of the lung, breast, prostate, pancreas, head, neck, or blood comprising a step of administering to a patient in need thereof an effective amount of a compound of Formula (I), or a pharmaceutically acceptable salt thereof.

[192] The invention also provides the use of a compound of Formula (I), or a pharmaceutically acceptable salt thereof, in the treatment of a condition as defined above.

[193] The invention also provides the use of a compound of Formula (I), or a pharmaceutically acceptable salt thereof, in the manufacture of a medicament for the treatment of a condition as defined above.

[194] In the methods of the invention the term "treatment" includes both therapeutic and prophylactic treatment.

[195] The compounds of Formula (I), or pharmaceutically acceptable salts thereof, may be administered alone or in combination with one or more other therapeutically active compounds. The other therapeutically active compounds may be for the treatment of the same disease or condition as the compounds of Formula (I) or a different disease or condition.

The therapeutically active compounds may be administered simultaneously, sequentially or separately.

[196] The compounds of Formula (I) may be administered with other active compounds for the treatment of cancers of the lung, breast, prostate, pancreas, head, neck, or blood - for example AVASTIN, IRESSA, TARCEVA, ERBITUX, or cisplatin.

[197] The compounds of Formula (I) may also be administered in combination with

AVASTIN, IRESSA, TARCEVA, ERBITUX, or cisplatin.

[198] The compounds of Formula (I) may exhibit advantageous properties compared to known kinase inhibitors, for example, the compounds may exhibit improved solubility thus improving absorption properties and bioavailability. Furthermore the compounds of Formula (I) may exhibit further advantageous properties such as reduced inhibition of cytochrome P450 enzymes, meaning that they are less likely to cause adverse drug-drug interactions than known kinase inhibitors.

EXPERIMENTAL

[199] Scheme 1 - Scheme 5, the EXAMPLES, and INTERMEDIATES serve to demonstrate how to synthesize compounds of this invention, but in no way limit the invention.

[200] The following abbreviations are used:

NMR Nuclear magnetic resonance

LC/MS Liquid chromatography mass spectrometry LDA Lithium diisopropylamide

DCM Dichloromethane

THF Tetrahydrofuran

MeCN Acetonitrile

DMSO Dimethylsulfoxide

BOC or Boc t-butyloxycarbonyl

PyBrop Bromotri(pyrrolidino)phosphonium hexafluorophosphate

DMF N, N-dimethylformamide

PS-DIEA Polymer supported diisopropylethylamine

EDCI or EDC l-(3-dimeώylaminopropyl)-3-ethylcarbodiimide

HOBt 1 -hydroxybenzotriazole

DMAP 4-dimethylaminopyridine

HATU 0-(7-azabenzo1riazol-l-yl)-N,N,NW'-tetramemyluronium hexafluorophosphate

Ex Example

TLC Thin layer chromatography

Min or mins minute(s)

Hr, hrs, or h hour(s)

RT, rt, or r.t room temperature

Rt, or t_R Retention time

DESCRIPTION OF THE CHEMISTRY

I-A

[201] Compound of Formula I-A is equal to compound of Formula I wherein X =

N, Cy

, and Y, Rl, and Z are as defined above for Formula (I).

I-B [202] Compound of Formula I-B is equal to compound of Formula I wherein X =

N, Cy =

, YRl = NR1R2, and Rl, R2, and Z are as defined above for

Formula (I).

[203] Scheme 1 below describes how compounds of Formula I-A may be synthesized.

Scheme 1

[204] Compound of Formula II is commercially available or can be prepared by methods described in the literature (e.g., J. Chem. Soc. 1960, 131-138; J. Heterocyclic Chem. 1969, 6(2), 207-213). A benzenesulfonyl group is introduced under typical reaction conditions with typical bases and sulfonylating reagents in typical solvents to give compound of Formula III. Typical reagents and solvents include, but are not limited to, sodium hydride in DMF or THF, alkoxides such as potassium tert-butoxiάe in THF, a biphasic system consisting of aqueous NaOH and methylene chloride. Typical sulfonylating reagents are, e.g., benzenesulfonyl chloride or the corresponding anhydride. Typical conditions include, but are not limited to, -2O⁰C to RT, at atmospheric pressure, with equimolar amounts of base and sulfonylating reagent, although larger amounts can be used if desirable. Compounds of Formula III can be iodinated under typical metallation / iodination conditions to yield compounds of Formula IV. Typical conditions include, but are not limited to, adding a lithium amide base, such as LDA or LiTMP, to a cooled (about -78⁰C to about O⁰C) solution of compound of Formula III in an ether-type solvent, such as THF, 2-methyl-THF, DME, and the like (optionally containing other solvents such as aliphatic or aromatic hydrocarbons), and reacting the resulting species with an iodine source such as I₂, ICl, or N-iodosuccinimide. Compounds of Formula V can be prepared from compounds of Formula IV by reacting with bases such as NaOH in alcoholic solvents such as MeOH at typical reaction temperatures from about -10⁰C to about 4O⁰C. Compounds of Formula VIII can be prepared by palladium- mediated coupling with a boronate of Formula VI under typical Suzuki conditions well known to someone skilled in the art. It will be appreciated that instead of the pinacol boronate shown, other boronate esters or the free boronic acids may also be used. Furthermore, reaction of the corresponding trialkyl tin derivatives of VI (i.e., compounds with, e.g., Bu₃Sn- in place of the pinacolboronate) under typical Stille coupling conditions may also be used to prepare compounds of Formula VIII from compounds of Formula V. In an alternative route, compound of Formula III can be reacted with a strong base such as LDA, lithium tetramethylpiperidide, or the like, in an ether-type solvent such as THF, DME, and the like, and then reacted with a protected 4-piperidone VII, to give compounds of Formula VIII directly. Displacement of the chloride of compounds of Formula VIII with HYRl under typical chloride displacement conditions gives compounds of Formula I- A. Alternatively, the order of steps may be reversed: Compound of Formula V is first reacted with HYRl under typical chloride displacement conditions to yield compounds of Formula IX, followed by palladium-mediated coupling with a boronate of Formula VI under typical Suzuki conditions as described above to give compounds of Formula I-A.

[205] If deemed advantageous, the removal of the benzesulfonyl group may also be performed after chloride displacement and Suzuki coupling under substantially similar reaction conditions. Someone skilled in the art will realize that other groups may be used in place of the benzenesulfonyl group for the metalation / iodination reaction. Examples include, but are not limited to, toluenesulfonyl, fert-butoxycarbonyl, and fert-butylcarbamoyl. Furthermore, instead of introducing an iodine in the reaction from compound of Formula III to compound of Formula IV one may introduce a bromine using, e.g., bromine, CBr₄, or NBS under otherwise identical conditions and react the resulting compound in the same way as described above.

[206] Further manipulation of the substituents Z may be desirable, and Scheme 2 below describes how compounds wherein Z = tert-butoxycarbonyl (Boc) may be used for that purpose.

Scheme 2

[207] Compound of Formula I-A-Boc can be reacted with HCl in a typical solvent to give the hydrochloride salt of Formula I-A-H. Typical solvents include, but are not limited to, dioxane, MeOH, and water. Compounds of Formula I-A-H can be reacted with acids, anhydrides, acid halids, chloroformates, carbamoyl halides, sulfonyl halides, sulfamoyl halids, sulfonic anhydrides, and the like, under conditions described in the examples to give compounds of Formula I-A. Alternatively, a compound of Formula VIII-Boc can be reacted with HCl as described above to give the hydrochloride salt of Formula X. Introduction of the Z substituents as described above to yield a compound of Formula VIII, followed by chloride displacement with HYRl gives compounds of Formula I-A.

[208] Someone skilled in the art will realize that acids other than HCl can be used for removal of the Boc group in compounds of Formula VIII-Boc and I-A-Boc. [209] When HYRl is equal to HNR1R2, someone skilled in the art will recognize that a variety of typical reaction conditions, typical solvents, and typical additives are available for the conversion of VIII to I-B and of VIII-Boc to I-B-Boc, shown in Scheme 3.

Scheme 3

[210] Generally, VIII or VIII-Boc are reacted with HNR1R2 in a suitable solvent.

Typical solvents include, but are not limited to, alcohols such as ethanol, isopropyl alcohol, butanol, or trifluoroethanol (TFE); or polar solvents such as DMF, NMP, or DMSO. If deemed necessary, typical additives such as HCl and TFA may be added. The reaction is typically carried out at about 4O⁰C to about 15O⁰C. If a relatively low boiling alcohol is used as solvent, it may be advisable to conduct the reaction in a pressure reactor. Alternatively, typical transition-metal mediated chloride displacement conditions well known to someone skilled in the art can be used. These conditions typically involve reacting VIII or VIII-Boc with HNRl R2, a transition metal compound, a suitable ligand, and a base in a suitable solvent. Someone skilled in the art will recognize that especially when acidic additives are used, the Boc group may be partially or completely removed simultaneously, so that compounds of Formula I-B-H are solely obtained or in a mixture with compounds of Formula I-B-Boc. If one wishes to obtain compounds of Formula I-B-Boc, the reaction mixture containing compounds of Formula I-B-H (either exclusively or as mixture with compounds of Formula I-B-Boc) can directly be treated with a base such as triethylamine or diisopropylethylamine and di-tert-butyldicarbonate without the need for isolation. If one wishes to obtain compounds of Formula I-B-H, a mixture with compounds of Formula I-B- Boc can directly be treated with suitable acids to remove the Boc group completely. [211] In some cases, compounds of Formula HNR1R2 are commercially available or synthesized according to literature procedures. In cases where neither is available, compounds of Formula HNR1R2 were synthesized via procedures described in the experimental section herein.

[212] Compound of Formula I-C is equal to compound of Formula I wherein X =

C-CN, Cy =

, YRl =NR1R2, and Rl, R2, and Z are as defined above for

Formula (I).

[213] Scheme 4 below describes how compounds of Formula I-C may be synthesized.

Scheme 4

[214] The compound of Formula XII is known in the literature and may be prepared according to a published procedure (Tetrahedron Lett. 2004, 45, 2317-2319). Typical conditions for the removal of the triisopropylsilyl group to obtain compound of Formula XIII include, but are not limited to, treatment with tetrabutylammonium fluoride, or acids such as HCl or H₂SO₄ in alcoholic solvents. A compound of Formula XIV may be obtained from a compound of Formula XIII as described above for the conversion of a compound of Formula II to a compound of Formula III. A compound of Formula XV may be obtained from a compound of Formula XIV as described above for the conversion of a compound of Formula III to a compound of Formula IV. Compounds of Formula XVI can be obtained by reacting compound of Formula XV with HNRl R2 in a typical solvent under typical reaction conditions. Typical solvents include, but are not limited to, alcohols such as trifiuoroethanol (TFE) with additives such as HCl and TFA. The reaction is typically carried out at about 4O⁰C to about 12O⁰C. If the reaction temperature is higher than the boiling point of the reaction mixture, a pressure reactor should be used. The benzenesulfonyl group of compounds of Formula XVI can be removed to give compounds of Formula XVII under conditions described above for the conversion of a compound of Formula IV to a compound of Formula V. Compounds of Formula XIX can be prepared from compounds of Formula XVII by palladium-mediated coupling with a boronate of Formula VI under typical Suzuki conditions well known to someone skilled in the art. It will be appreciated that instead of the pinacol boronate shown, other boronate esters or the free boronic acids may also be used. Furthermore, reaction of the corresponding trialkyl tin derivatives of VI (i.e., compounds with, e.g., Bu₃Sn- in place of the pinacolboronate) under typical Stille coupling conditions may also be used to prepare compounds of Formula XVII from compounds of Formula XVI. Alternatively, the benzesulfonyl group in compound of Formula XV may be removed first to yield compound of Formula XVIII, followed by coupling with a boronate of Formula VI to give compounds of Formula XX, and chloride displacement with HNRl R2 to give compounds of Formula XIX, under conditions described above. Finally, compounds of Formula I-C may be obtained from compounds of Formula XIX by transition metal-mediated conversion of the bromo to the cyano substituents. Typical conditions include, but are not limited to, reaction with Pd₂dba₃, dppf, and Zn(CN)₂ in DMF/water. [215] Someone skilled in the art will realize that other groups may be used in place of the benzenesulfonyl group for the metalation / iodination reaction. Examples include, but are not limited to, toluenesulfonyl, tert-butoxycarbonyl, and tert-butylcarbamoyl. Furthermore, if Z = Boc, the chloride displacement in compounds of Formula XX under the conditions described above may lead to removal of the Boc group to give a compound of Formula XIX wherein Z = H. Such a compound can be treated with a base such as triethylamine or diisopropylethylamine and di-tert-butyldicarbonate to obtain a compound of Formula XIX wherein Z = Boc, or with other appropriate reagents to introduce the desired Z substituent. [216] Further manipulation of the substituents Z may be desirable, and Scheme 5 below describes how compounds wherein Z = tert-butoxycarbonyl (Boc) may be used for that purpose.

Scheme 5

[217] Compounds of Formula XX-Boc, XIX-Boc, or I-C-Boc can be reacted with

HCl in a typical solvent to give the hydrochloride salt of Formula XX-H, XIX-H, or I-C-H, respectively. Typical solvents include, but are not limited to, dioxane, MeOH, and water. Compounds of Formula XX-H, XIX-H, or I-C-H can be reacted with acids, anhydrides, acid halids, chloroformates, carbamoyl halides, sulfonyl halides, sulfamoyl halids, sulfonic anhydrides, and the like, under conditions described in the examples to give compounds of Formula XX, XIX, or I-C, respectively. Someone skilled in the art will realize that acids other than HCl can be used for removal of the Boc group in compounds of Formula XX-Boc, XIX-Boc, and I-C-Boc.

[218] It would be appreciated by those skilled in the art that in some situations, a substituent that is identical or has the same reactivity to a functional group which has been modified in one of the following processes, will have to undergo protection followed by deprotection to afford the desired product and avoid undesired side reactions. Alternatively, another of the processes described within this invention may be employed in order to avoid competing functional groups. Examples of suitable protecting groups and methods for their addition and removal may be found in the following reference: "Protective Groups in Organic Syntheses", T. W. Greene and P. G. M. Wuts, John Wiley and Sons, 1989. [219] All melting points were deteπnined with a Mel-Temp II apparatus and are uncorrected. Commercially available anhydrous solvents and HPLC-grade solvents were used without further purification. ¹H NMR and ¹³C NMR spectra were recorded with Varian or Bruker instruments (400 MHz for ¹H, 100.6 MHz for ¹³C) at rt with TMS or the residual solvent peak as internal standards. The line positions or multiplets are given in ppm (δ) and the coupling constants (J) are given as absolute values in Hertz, while the multiplicities in ¹H NMR spectra are abbreviated as follows: s (singlet), d (doublet), t (triplet), q (quartet), quint (quintet), m (multiple:), In₀ (centered multiplet), br (broadened), AA'BB'. The signal multiplicities in ¹³C NMR spectra were determined using the DEPTl 35 pulse sequence and are abbreviated as follows: + (CH or CH₃), - (CH₂), C_quart (C). LC/MS analysis was performed using a Gilson 215 autosampler and Gilson 819 autoinjector attached to a Hewlett Packard HPl 100 and a Micromass ZQ2000 mass spectrometer. XTERRA MS C18 5μ 4.6x50mm columns with detection at 254 nm and electrospray ionization in positive mode were used. For mass-directed purification (MDP), a Waters / MicromassZQ system was used. [220] The tables below list the mobile phase gradients (solvent A: acetonitrile; solvent B: 0.01% formic acid in HPLC water) and flow rates for the analytical HPLC programs.

Polar 5min

Flow Rate

Time A% B% (mL/min) MicromassZQ

0.00 5 95 1.3

3.00 90 10 1.3

3.50 90 10 1.3

4.00 5 95 1.3

5.00 5 95 1.3

Polar_15min

Flow Rate

Time A% B% (mL/min) MicromassZQ

0.00 5 95 1.3

1.00 30 70 1.3

7.50 90 10 1.3

10.00 100 0 1.3

13.00 5 95

15.00 5 95 1.3

Nonpolar_5min

Flow Rate

Time A% B% (mL/min) MicromassZQ

0.00 25 75 1.3

3.00 99 1 1.3 Flow Rate

Time A% B% (mL/min) Micro massZQ

3.S0 99 1 1.3

4.00 25 75 1.3

5.00 25 75 1.3

Nonpolar_ 7min

Flow Rate

Time A% B% (mL/min) Micro massZQ

0.00 25 75 1.3

4.00 100 0 1.3

5.50 100 0 1.3

6.00 25 75 1.3

7.00 25 75 1.3

Nonpolar_l 5min

Flow Rate

Time A% B% (mL/min) Micro massZQ

0.00 15 85 1.3

7.50 99 1 1.3

11.00 99 1 1.3

12.50 15 85 1.3

15.00 15 85 1.3

Syntheses of EXAMPLES and INTERMEDIATES

[221] 4-Chloro-7-(phenylsulfonyl)-7H-pyrroIo[2,3-rf]pyrimidine (compound of Formula II).

[222] To a solution of 4-chloro-7H-pyrrolo[2,3-φyrimidine (1Og, 0.065mol) in

THF (30OmL) was added potassium tert-butoxide (9.15g, 0.082mol) at r.t. over 5min. A slight exotherm was noticed and suspension was cooled with the aid of a water bath. Benzenesulfonyl chloride (10.5mL, 0.082mol) was then added drop-wise over a period of lOmin and the resulting suspension stirred for a further 3h. Then water (2OmL) was added drop-wise and the solution was then stirred for 15min. The solvent was evaporated under reduced pressure and the reaction mixture was eluted with ethyl acetate (1.21), washed with brine (2 x 10OmL), dried and concentrated. The resulting solid was triturated with ethyl acetate (5OmL) to afford 4-chloro-7-(phenylsulfonyl)-7H-pyrrolo[2,3-d]pyrimidine as an off- white solid. ¹H NMR (CDCl₃, 400 MHz) δ 6.75 (IH, d), 7.55-7.625 (2H, t), 7.70 (IH, t), 7.82 (IH, d), 8.25 (IH, d) and 8.80 (IH, s).

[223] 4-Chloro-6-iodo-7-(phenylsulfonyI)-7H-pyrrolo[2,3-rf]pyrimidine

(compound of Formula III).

[224] To a stirred solution of 4-chloro-7-(phenylsulfonyl)-7H-pyrrolo[2,3-d]- pyrimidine (5.0g, 0.017mol) in TΗF (20OmL) under inert atmosphere, at -78°C, was added 2.0M LDA solution (9.8mL, 0.0195mol) over a period of 15min. After Ih a solution of iodine (4.97g, 0.0196mol) in TΗF (5OmL) was added dropwise over a period of 15min. The resulting solution was stirred for a further 3h. Water (1OmL) was then added and the mixture allowed to reach r.t. The mixture was diluted with DCM (11), washed with brine (2 x 10OmL), dried and concentrated under reduced pressure. The resulting solid was triturated with MeCN to afford the 4-chloro-6-iodo-7-(phenylsulfonyl)-7H-pyrrolo[2,3-rf]pyrimidine. ¹H NMR (CDCl₃, 400 MHz) 7.05 (IH, s), 7.50 (2H, t), 7.60 (IH, t), 8.20 (2H, d) and 8,65 (lH, br s).

[225] 4-ChIoro-6-iodo-7i3-pyrrolo [2,3-rf] pyrimidine (compound of Formula IV).

[226] To a stirred solution of djpyrimidine (538mg, 1.283mmol) in TΗF (6.OmL) was added 5M sodium hydroxide methanolic solution (1.8mL, 0.009mmol). After lOmin the solvent was removed under reduced pressure, sat. ammonium chloride solution (5.OmL) was added and the mixture evaporated to dryness. The resulting solid was triturated with water to afford 4-chloro-6- iodo-7H-pyrrolo[2,3-φyrimidine. 1Η NMR (d₆-DMSO, 400 MHz) 6.90(1H, s) and 8.55 (IH, s). [227] te^-ButyI 4-(4-chloro-7Jy-pyrrolo[2,3-«qpyrimidm-6-yl)-3,6- dihydropyridine-l(2fi)-carboxylate (compound of Formula VIII-Boc).

[228] To a suspension of 4-chloro-6-iodo-7H-pyrrolo[2,3-d]pyrimidine (5.Og,

0.018mol) in 1,4-dioxane (12OmL) and water (3OmL) were added 4-(4,4,5,5-tetramethyl- [l,3,2]dioxaborolan-2-yl)-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester (5.97g, 0.0193mol), potassium carbonate (4.9g, 0.036mol) and PdCl₂(dppf)- CH₂Cl₂ (0.73g, 0.89mmol). The flask was evacuated and refilled with N₂ (3x). The mixture was heated at 100°C overnight. LC-MS showed the reaction was complete. The mixture was diluted with ethyl acetate (20OmL), then washed with brine (2x50mL), and dried over anhydrous sodium sulfate. The filtrate was concentrated under reduced pressure to ∞lOOmL, the resulting white precipitate was collected by filtration to give the first batch of the title compound. The filtrate was concentrated and the residue was purified by chromatography on silica gel, eluting with Hex:EtOAc = 70:30 → 50:50 to give a white solid (containing pinacol), which was further crystallized with EtOAc/hexanes to give the second batch of the title compound as a white solid. LC-MS (ES, Pos.): 335/337 (3/1) [MH⁺]. ¹H NMR (CDCl₃, 400 MHz): δ = 1.51 (s, 9H), 2.61 (m, 2H), 3.70 (m, 2H), 4.20 (m, 2H), 6.27 (s, IH), 6.55 (s, IH), 8.61 (s, IH), 10.3 (brs, IH).

[229] Alternative synthesis: To a -78⁰C solution of 4-chloro-7- phenylbenzenesulfonyl-7H-pyriOlo[2,3-J]pyrimidine (1.0Og, 3.41mmol) in anhydrous THF (15mL) was added LDA solution (1.5M in cyclohexanes; 3.4ImL, 5.12mmol) dropwise over 5min. The mixture was left to stir for Ih after which time l-Boc-4-piperidone (0.82g, 4.09mmol) was added as a solution in THF (5mL) and the mixture left to warm to rt over a weekend. The solution was diluted with EtOAc (15OmL) and partitioned over water. The organic layer was washed with brine, dried (MgSO₄), filtered and concentrated in vacuo. Purification by column chromatography on silica gel loading in DCM and eluting with 5 : 1 Hexanes:EtOAc stepwise to EtOAc yielded the title compound as an off-white powder.

[230] General method for the reaction of amines with tert-butyl 4-(4-chloro-7H- pyrrolo[2, 3-d]pyrimidin-6-yl)-3, 6-dihydropyridine-l(2H)-carboxylate to generate compounds of Formula I-B-Boc:

[231] Amine HNR1R2 (0.215mmol) was added to a solution of tent-butyl 4-(4- chloro-7H-pyrrolo[2,3-(f]pyrimidin-6-yl)-3,6-dihydropyridine-l (2H)-carboxylate (0.18mmol) in butanol (4mL). The reaction was heated to 95⁰C for 2h. If the reaction was incomplete the reaction temperature was increased to 105⁰C, and if required to 115°C, until all the starting material was consumed. The solvent was removed and the residue purified on silica gel by elution with dichloromethane: methanol to yield the product of Formula I-B-Boc. Alternatively, purification may be possible by HPLC, crystallization, or trituration. [232] The following EXAMPLES were prepared using the general method described above. In Table 1, reference is to formula I-B-Boc:

I-B-Boc

[233] Table 1. .

[234] Alternative synthesis of 4-[4-(Benzothiazol-6-ylamino)-7Jϊ-pyrroIo[2,3-

^pyrimidin-6~yI]-3,6-dihydro-2iir-pyridine-l-carboxyIic acid tert-butyl ester (EXAMPLE 1):

[235] PdCl₂CdPPf)₂-CH₂Cl₂ (8.2mg, O.OlOmmol) was added into the mixture of benzothiazol-6-yl-(6-iodo-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-amine (78.7mg, 0.200mmol), 4- (4,4,5,5-tetramethyl-[l,3,2]dioxaborolan-2-yl)-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester (68.0mg, 0.220mmol), and K₂CO₃ (55.3mg, 2.00mmol) in DMF:Η₂O (2.5mL:0.5mL). The combined mixture was bubbled with N₂ for 5min and was then heated at 10O⁰C under N₂ for 16h. After that time, the mixture was concentrated in vacuo and purified by MS directed purification. One obtained the title compound as light brown solid. ¹H NMR (CD₃OD, 400 MHz): δ 1.40 (s, 9 H), 2.49 (bis, 2 H), 3.57 (bra, 2 H), 4.03 (brs, 2 H), 6.20 (brs, 1 H), 6.61 (s, 1 H), 7.68 (dd, 1 H, J= 2.0 & 8.8 Hz), 7.90 (d, 1 H, J= 8.8 Hz), 8.19 (s, 1 H), 8.64 (d, 1 H, J= 2.0 Hz), 9.02 (s, 1 H). MS (ES+): m/z 449 (100) [MH⁺]. [236] Benzothiazol-6-yl-(6-iodo-7H-pyrrolo[2,3-rf]pyrimidin-4-yI)-amine

(compound of Formula IX wherein Rl = benzothiazol-6-yl and Y = NH).

[237] Following the General method for the reaction of amines with tert-butyl 4-(4- chloro-7H-pyrrolo[2,3-d]pyrimidin-6-yl)-3,6-dihydropyridine-l(2H)-carboxylate to generate compounds of Formula I-B-Boc, but using 4-chloro-6-iodo-7H-pyrrolo[2,3-rf]pyrimidine and benzothiazol-6-ylamine, one obtained the title compound. MS (ES+): m/z 393.88 (100) [MH⁺].

[238] Example 44: 4-[4-(lH-Indazol-5-ylamino)-7H-pyrrolo[2,3-d]pyrimidin-

6-yI]-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester.

[239] A mixture of 4-(4-chloro-7H-pyrrolo[2,3-rf]pyrimidin-6-yl)-3,6-dihydro-2H- pyridine-1-carboxylic acid tert-butyl ester (136mg, 0.41mmol) and 5-aminoindazole (65mg, 0.49mmol) in W-BuOH (2mL) were heated at 12O⁰C for 3h, then cooled and the solvent removed in vacuo. The mixture was dissolved in DMSO/MeOH and purified by RP-HPLC (gradient 5 to 75 % MeCNTH₂O over 15min, 0.01 % formic acid as buffer, flow rate 15mL/min). Upon concentration of desired fractions, a white powder precipitated that was filtered, washed with ether and dried in vacuo to reveal the title compound. ¹H NMR (400 MHz, DMSO-d⁶): δ = 1.42 (s, 9H), 2.44 (brs, 2H), 3.55 (bis, 2H), 4.03 (bra, 2H), 6.39 (bra, IH), 6.76 (brs, IH), 7.53-7.60 (m, 2H), 8.06 (s, IH), 8.21-8.30 (m, 2H), 9.78 (brs, IH)₁ 12.08 (brs, IH). MS (ES+): m/z 432.2 (20) [MH⁺].

General method for removal of the Boc protecting group:

[240] Compound of Formula I-B-Boc (leq) was added to HCl in dioxane (4M)

(20equiv) at rt. After 18h the resultant solid was filtered off to yield the hydrochloride solid I-

B-H.

[241] EXAMPLE 45: (liϊ-Indazol-5-yl)-[6-(l,2,3,6-tetrahydropyridin-4-yl)-

7i?-pyrrolo [2,3-d\ pyrimidin-4-yl] -amine.

[242] 4-[4-(lH-Indazol-5-ylamino)-7H-pyrrolo[2,3-d]pyrimidin-6-yl]-3,6-dihydro-

2H-pyridine-l-carboxylic acid tert-butyl ester (Ig, 2.32mmol) was added to 4M HCl in dioxane (16mL) and stirred for 18h. The solid was then filtered off, washed with ether and dried to yield the title compounds as an off-white solid. IH NMR (d₄Me0H, 400 MHz) 8.23 (IH, s), 8.2 (IH, s), 8.0 (IH, s), 7.8 (IH, d), 7.6 (IH, d), 6.85 (lH,br.s), 6.42 (IH, s), 4.0 (2H_; s), 3.5 (2H, m), 2.85 (2H, br. s).

[243] Alternative solvents for removal of the Boc group include, but are not limited to, MeOH and water, as demonstrated here with EXAMPLE 45: A suspension of tert-butyl 4-[4-(lH-indazol-5-ylammo)-7H-pyrrolo[2,3-^pyrrrrύdin-6-yl]-3,6-dmydro-2H-pyridine-l- carboxylate (670mg, 1.55mmol) in 4 N HCl (aq) (2OmL) was stirred at rt for 18h. The precipitates were collected by filtration and washed with ether (3x1 OmL) to afford (IH- indazol-5-yl)-[6-(l,2,3,64etrahydropyridin-4-yl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl]amine as tri-ΗCl salt. ¹H-NMR (DMSOd₆, 400 MHz): δ = 2.63 (m, 2 H), 3.30 (m, 2 H), 3.79 (m, 2 H), 6.52 (s, br, 1 H), 7.44 (dd, J= 2.0, 8.8 Hz, 1 H), 7.72 (d, /= 8.8 Hz, 1 H), 7.95 (s, 1 H), 8.18 (d, J= 1.2 Hz, 1 H), 8.26 (s, 1 H), 9.59 (s, 1 H). MS (ES+): m/z 332.12 [MH⁺]. HPLC: t_R = 0.44 and 1.37 min (ZQ2000, polar_5min).

[244] EXAMPLE 46: (lH-Indazol-5-yl)-[6-(l-methanesulfonyl-l,2,3,6- tetrahydropyridin-4-yl)-7H-pyrrolo[2,3-rf]pyrimidin-4-yI]-amine.

[245] (lΗ-Indazol-5-yl)-[6-(l,2,3,6-tetrahydro-pyridin-4-yl)-7Η-pyπOlo[2,3- d]pyrimidin-4-yl] -amine hydrochloride (80mg, 0.217mmol), Hunigs base (113μL, 0.653mmol) and methanesulfonyl chloride (17μL, 0.2177mmol) were combined in DMF at rt and stirred overnight. The reaction was concentrated in vacuo and residue purified on silica gel by elution with tetrahydrofuran:dichloromethane (3:2) to yield the title compound as white solid. IH NMR (d₆-DMSO, 400MHz) 9.4(1H, br. s), 8.4 (IH, s), 8.3(lH,s), 8.0(lH,s), 7.7(1H, d), 7.5(1H, d), 6.8(1H, s), 6.4(lH,s), 3.9(2H, s), 3.4(2H, m), 3.0(3H,s) and 2.6(2H, s); LC/MS: m/z 410 [M+H]⁺, Rt =2.82min.

[246] EXAMPLE 47: 2-Dimethylamino-l-{4-[4-(lH-indazol-5-ylamino)-7H- pyrrolo[2,3-rf]pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yl}-ethanone.

[247] (lH-Indazol-S-yO-tό-Cl^^^-tetraliydro-pyridin^-yO-VH-pyrroloCZ.S- d]pyrimidin-4-yl] -amine hydrochloride (80mg, 0.217mmol), N,N-dimethylglycine (22.4mg, 0.277mmol), PyBrop (lOlmg, 0.217mmol) and Hϋnigs base (113μL, 0.653mmol) were combined in DMF (3mL) and stirred at rt for 37h. The DMF was removed in vacuo and the residue was absorbed onto silica. Purification on silica gel by elution with tetrahydrofuran:methanol:conc ammonia (30:1:1) yielded a white solid. IH NMR (d₆-DMSO, 400MHz) Rotamers observed: 9.32 & 9.30 (IH, rotamers,2s), 8.37& 8.36 (IH, rotamers, 2s), 8.26 (IH, s), 8.0 (lH,s), 7.68 (2H,d), 7.53 (lH,d), 6.78 & 6.75 (IH, rotamers, 2s), 6.4 (IH, s), 4.3 (IH, s), 4.2(1H, s), 3.76 & 3.71 (2H, rotamers, 2t), 3.18 & 3.14 (2H, rotamers, 2s), 2.5 (2H, m), 2.23 & 2,21 (6H, rotamers, 2s); LC/MS: m/z 416 [MfH]⁺, Rt =2.52min.

[248] EXAMPLE 48: l-{4-[4-(lH-IndazoI-5-ylamino)-7_JH^r-pyrrolo[2,3-rfl- pyrimidin-6-yI]-3,6-dihydro-2H-pyridin-l-yl}-ethanone.

[249] (lH-Indazol-5-yl)-[6-(l,2,3,6-tetrahydro-pyridin-4-yl)-7H-pyrrolo[2,3- d]pyrimidin-4-yl] -amine hydrochloride (60mg, 0.137mmol), HATU (63mg, 0.164mmol) and Hunigs base (lOOμL, 0.576mmol) were combined in DMF (4mL) and stirred for 30min. Acetic acid (8μL, 0.168mmol) was added and the solution was stirred overnight. Another portion of acetic acid (8μL, 0.168mmol) was added and the stirred for a further 4h. The DMF was removed in vacuo and the residue was loaded onto silica. Purification on silica by elution with dichloromethane:methanol (95:5) yielded the title compound as a yellow solid. ¹H NMR (400 MHz, DMSO-d⁶): δ = 2.03 & 2.07 (2s, rotamers, 3H), 2.44 & 2.53 (2s, rotamers, 2H), 3.62-3.67 (m, 2H), 4.11 & 4.18 (2s, rotamers, 2H), 6.39 (s, IH), 6.72 & 6.76 (2s, rotamers, IH), 7.50 (d, J= 8.8 Hz, IH), 7.63 (d, J= 8.8 Hz, IH), 8.03 (s, IH), 8.24 (s, IH), 8.33 (brs, IH), 9.35 (brs, IH), 11.90 (brs, IH). MS (ES+): m/z 374.5 (100) [MH⁺].

[250] EXAMPLE 49: 2,2,2-Trifluoro-l-{4-[4-(l_Jfir-indazol-5-ylamino)-7H- pyrrolo[2,3-rf]pyrimidin-6-yI]-3,6-dihydro-2H-pyridin-l-yl}-ethanone.

[251] (lH-Indazol-5-yl)-[6-(l_!2,3,6-tetrahydro-pyridin-4-yl)-7H-pyrrolo[2,3- d]pyrimidin-4-yl] -amine hydrochloride (150mg, 0.34mmol), Hunigs base (239μL, 1.37mmol) and trifluoroacetic anhydride (96mL, 0.68mmol) were combined in DMF (6mL) and stirred overnight. Trifluoroacetic anhydride (96mL, 0.68mmol) was added and the mixture was stirred a further 2h. The DMF was removed in vacuo and the residue was partioned between dichloromethane and IM HCl (aq). The organic layer was separated and dried over anhydrous magnesium sulphate, filtered and evaporated in vacuo. Purification on silica gel by elution with ethyl acetate yielded the title compound as a yellow solid. ¹H NMR (400 MHz, DMSO-d⁶): δ = 2.58-2.64 (brm, 2H), 3.78-3.86 (m, 2H), 4.27 & 4.32 (2s, rotamers, 2H), 6.38 & 6.40 (2s, rotamers, IH), 6.76 & 6.80 (2s, rotamers, IH), 7.50 (d, J= 8.8 Hz, IH),^' 7.63 (ά, J= 8.8 Hz, IH), 8.03 (s, IH), 8.24 (s, IH), 8.32-8.35 (m, IH), 9.34 (s, IH), 11.95 (s, IH). MS (ES+): m/z 428.4 (100).

[252] EXAMPLE 50: 4-[4-(lH-IndoI-5-ylamino)-7H-pyrrolo[2,3-rf]pyrimidin-

6-yl]-3,6-dihydro~2H-pyridine-l-carboxylic acid tert-butyl ester.

[253] A suspension of 4-(4-chloro-7H-pyrrolo[2,3 -rf]pyrimidin-6-yl)-3 ,6-dihydro-

2H-pyridine-l-carboxylic acid te^-butyl ester (606.0mg, 1.810mmol, leq) and 5-aminoindole (548.9mg, 4.153mmol, 2.3eq) in Η-BUOΗ (3OmL) was stirred at 120⁰C for 23h, after which it was concentrated in vacuo, to a dark brown foam. The crude material (1.2974 g) was dissolved in mixtures of DCM and MeOH (DCM alone was insufficient), to which DiPEA (0.4mL, 2mmol, leq) was added to ensure that material was free base and not HCl salt. The crude material was adsorbed onto Ηydromatrix, dry loaded, and purified by chromatography on silica gel [Jones Flashmaster, 50g / 15OmL cartridge, eluting with MeOΗ:DCM 1% — > 5% — > 10%]. Trituration of combined and concentrated product fractions in DCM / sonication gave the title compound as white solid. ¹H NMR (400 MHz, DMSO-^₆): δ = 1.43 (s, 9H), 2.44 (s, br, 2H), 3.55 (t, J= 5.6 Hz, 2H), 4.03 (s, br, 2H), 6.35 (s, br, IH), 6.40 (t, /= 2.0 Hz, IH), 6.67 (s, br, IH), 7.29 -7.41 (m, 3H), 8.03 (s, br, IH), 8.19 (s, IH), 9.14 (s, -NH), 10.99 (s, -NH), 11.81 (d, J= 1.6 Hz, -NH). MS (ES+): m/z 431.04 (100) [MH⁺]. HPLC: t_R = 2.42 min (ZQ2000, polar_5min).

[254] Alternative preparation: 4-[7-Benzenesulfonyl-4-(lH-indol-5-ylamino)-7H- pyrrolo[2,3d]pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester (84mg, 0.147mmol) in THF (2mL) was treated with a 5M solution of NaOH in MeOH (ImL). After lOmin the reaction was evaporated to dryness and cone. NH₄Cl solution and water (enough to dissolve all inorganic salts) were added, the mixture was extracted with EtOAc (3 x 4mL), the combined organic was washed with brine, dried over anhydrous magnesium sulphate, filtered, and concentrated to leave the title compound as pale pink solid. [255] 4-[7-Benzenesulfonyl-4-(lH-indol-5-ylamino)-7H-pyrrolo[2,3-rf|- pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester.

[256] 4-(7-Benzenesulfonyl-4-chloro-7H-pyrrolo[2,3-d]pyrimidin-6-yl)-3,6- dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester (150mg, 0.31mmol) in butanol (5mL) was treated with 5-aminoindole (50mg, 0.38mmol) and heated to 80⁰C for 2h and then 85⁰C for Ih. The mixture was evaporated to dryness and pre-absorbed onto silica. Purifcation on silica by elution with dichloromethane:methanol (97:3) yielded a slightly pink solid. IH NMR (d₆-DMS0, 400MHz) 9.4(NH), 8.3(1H, s), 8.0(2H,d), 7.9(lH,s), 7.7(lH,m), 7.6(2H,m), 7.4(2H,m), 7.2(lH,m), 6.8(1H, br.s), 6.4(1H, s), 6.0(lH,s), 4.1(2H, m), 3.6(2H,m), 2.5(2H, m), and 1.5(9H, s); LC/MS: m/z 570 [M+H]⁺, Rt = 4.07 min.

[257] 4-(7-Benzenesulfonyl-4-chloro-7H-pyrroIo[2,3-^pyrimidin-6-yl)-3,6~ dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester.

[258] 7-Benzenesulfonyl-4-chloro-6-iodo-7H-pyrrolo[2,3-d]pyrimidine (4.05g,

9.65mmol), 4-(4,4,5,5-tetramethyl-[l,3,2]dioxaborolan-2-yl)-3,6-dihydro-2H-pyridine-l- carboxylic acid tert-butyl ester (2.985g, 9.65mmol), potassium carbonate (2.935g, 21.25mmol) and dichlorobis(triphenylphosphine)-palladium(II) (678mg, 0.96mmol) were combined in dioxane/water (85mL:21mL) and heated to 90⁰C for 2h. After cooling the reaction mixture was extracted with ethyl acetate (3 x50mL), the organic layers were combined and washed with aqueous sodium bicarbonate, brine and finally water. The organic layer was dried over anhydrous magnesium sulphate, Filtered and pre-absorbed onto silica in vacuo. Purification on silica gel by gradient elution with isohexane:ethyl acetate (6:1) finishing with isohexane:ethyl acetate (4:1) yielded a yellow solid. IH NMR (d₆-DMSO, 400MHz) 8.8(1H, s), 8.0 (2H, d), 7.8(lH,m), 7.6(2H,m), 6.8(1H, s), 6.0(1H, s), 4.1(2H, br. s), 3.6(2H,m), 2.5(2H, br. s), and 1.5(9H, s); LC/MS: m/z AlA [M+H]⁺, Rt =4.42min

[259] Functionalisation of (lH-Indazol-5-yl)-[6-(l ,2,3,6-tetrahydropyridin-4-yl)-

7H-pyrrolo[2,3-d]pyrimidin-4-yl]-aniine hydrochloride (compound of Formula I-B-H wherein

R2 = H and Rl = indazol-5-yl) to yield compounds of Formula I-B wherein R2 = H, Rl = indazol-5-yl, and Z is as defined previously:

[260] Preferred method with Acid Chlorides, Chloroformates, Carbamoyl

Chlorides, Sulfamoyl chlorides, Sulfonyl chlorides & Isocyanates.

[261] To a solution of lH-indazol-5-yl-[6-(l,2,3,6-tetrahydropyridin-4-yl)-7H- pyrrolo[2,3-d]pyrimidin-4-yl]-amine hydrochloride (40mg, 0.1 lmmol) in DMF (1.5mL) was added diisopropylemylarnine (57μL, 3eq., 0.33mmol) at r.t, followed by the appropriate capping reagent (acid chloride, chloroformate, carbamoyl chloride, sulfamoyl chloride, sulfonyl chloride or isocyanate) (leq., 0.1 lmmol). The reaction was stirred at r.t. overnight.

After this time, the reaction was quenched with methanol (0.5mL) and the solvent was evaporated under reduced pressure. The resultant residue was purified by mass-directed

ΗPLC using water / acetonitrile mixtures optionally containing formic acid, trifluoroacetic acid, or ammonium carbonate to optimize separation.

[262] (Alternative methods including the use of polymer-supported diisopropylethylamine (PS-DIEA) under the conditions outlined above, or use of the free base lΗ-indazol-5-yl-[6-(l,2₎3,6-tetrahydropyridin-4-yl)-7Η-pyrrolo[2,3-d]pyrimidin-4-yl]-amine

(prepared by stirring of lH-indazol-5-yl-[6-(l,2,3,6-tetrahydropyridin-4-yl)-7H-pyrrolo[2,3- d]pyrimidin-4-yl] -amine hydrochloride with MP-Carbonate resin in methanol over 2h at r.t.) with reduced amounts of diisopropylethylamine present (leq.) were also used to prepare some of the compounds described).

[263] Preferred method with Carboxylic Acids.

[264] To a mixture of the appropriate carboxylic acid (leq., 0.1088mmol), 1-ethyl-

3-(3'-dimethylaminopropyl)carbodiimide hydrochloride (EDCIΗC1) (31.3mg., 1.5eq.,

0.163mmol), N-hydroxybenzotriazole monohydrate (HOBt-H₂O) (22.1mg., 1.5eq.,

0.163mmol) and a catalytic amount of 4-dimethylaminopyridine (DMAP) was added DMF

(2mL) followed by triethylamine (54μL, 3.5eq., O.38mmol). The solution was stirred at r.t. for 5min before lH-indazol-5-yl-[6-(l,2,3,6-tetrahydropyridin-4-yl)-7H-pyrrolo[2,3-d]- pyrimidin-4-yl] -amine hydrochloride (40mg, 0.1 lmmol) was added in a single portion. The reaction was stirred at r.t. overnight. After this time, the reaction was diluted with ethyl acetate (5mL) and an aqueous solution of sodium bicarbonate (2mL). The organic layer was collected and the aqueous layer extracted with ethyl acetate (2 x 5mL). The combined organic layer was washed with water (2mL), dried over anhydrous magnesium sulphate, filtered and the solvent was evaporated under reduced pressure. The resultant residue was purified by mass-directed HPLC. Alternatively, crude reaction mixtures were taken directly, the solvent was evaporated under reduced pressure and the residue was purified by mass- directed HPLC.

[265] (An alternative method using the free base lH-indazol-5-yl-[6-(l,2,3,6- tetxahydropyridin-4-yl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl]-amine (prepared by stirring of IH- indazol-5-yl-[6-(l,2,3,6-tetrahydropyridin-4-yl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl]-amine hydrochloride with MP-Carbonate resin in methanol over 2h at r.t.) with reduced amounts of triethylamine (1.5eq.) was also used to prepare some of the compounds described).

[266] Table 2: Examples of compounds prepared by functionalisation of (IH- indazol-5-yl)-[6-(l,2,3,6-te1xahydro-pyridin-4-yl)-7H-pyrrolo[2,3-d]pyrirnidin-4-yl]-amine hydrochloride or (lH-indazol-5-yl)-[6-(l,2,3,6-tetrahydro-pyridin-4-yl)-7H-pyrrolo[2,3- d]pyrimidin-4-yl] -amine (prepared by stirring of (lH-indazol-5-yl)-[6-(l,2,3,6-tetrahydro- pyridin-4-yl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl]-amine, as described above.

[267] Table 2

[268] EXAMPLE 63: {6-[l-(2-Chloropyrimidin-4-yl)-l,2,3,6-tetra- hydropyridin-4-yl]-7H-pyrro!o[2,3-d]pyriraidin-4-yl}-(lJϊ-indazol-5-yl)-amine.

[269] Following the Preferred method with Acid Chlorides, Chloroformates,

Carbamoyl Chlorides, Sulfamoyl chlorides, Sulfonyl chlorides & Isocyanates, but using 2,4- dichloropyrimidine as capping reagent, one obtained the title compound. MS (ES+): m/z 444.03/446.06 (38/13) [MH⁺]. HPLC: t_R = 2.21 min (ZQ2000, polar_5min).

[270] Following the Preferred method with Acid Chlorides, Chloroformates,

Carbamoyl Chlorides, Sulfamoyl chlorides, Sulfonyl chlorides & Isocyanates, using benzoMazol-6-yl-[6-(l,2,3,64etrahydropyridin-4-yl)-7H-pyrrolo[2,3-cT]pyrimidin-4-yl]amine trihydrochloride and the appropriate capping reagent, one obtained the examples listed in TABLE 3.

[272] EXAMPLE 76: 4-[4-(l#-IndazoI-5-ylamino)-7#-pyrrolo[2,3-rf]- pyrimidin-6-yl]-piperidine-l-carboxylic acid tert-butyl ester.

[273] A rapidly stirred mixture of 4-[4-(lH-indazol-5-ylamino)-7H-pyrrolo[2,3- d]pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester (O.lg) and 10% palladium on carbon (lOmg) was heated in ethanol (2OmL) at 100⁰C under a IOOPSI hydrogen atmosphere for 6h. After this time the mixture was cooled, filtered through celite and concentrated. Crystallisation from methanol/ethyl acetate afforded the title compound. IHNMR (300MHz, DMSO) δ = 1.44 (9H, s), 1.55 (IH, m), 2.0 (2H, m), 2.89 (3H, m), 4.06 (2H, m), 6.46 (IH₅ s), 7.52 (IH, d), 7.66 (IH, d), 8.07 (IH, s), 8.12 (IH, s), 8.18 (IH, s) and 9.15 (IH, s). MH⁺ 434.16.

[274] EXAMPLE 77: 4-[4-(lH-Indazol~5~ylamino)-7H-pyrroIo[2,3-tfI- pyrimidin-6-yl]-l-(2-methyoxyethyl)-l/?-pyridin-2-one.

[275] A mixture of (lH-indazol-5-yl)-(6-iodo-7H-pyrrolo[2,3-d]pyrimidin-4-yl)- amine (0.076g), l-(2-methoxy-ethyl)-2-oxo-l,2-dihydro-pyridine-4-boronic acid (36mg), PdC12(PPh3)2 (7mg) and potassium carbonate (76mg) in dioxane/water (4:1) (5mL) was heated to 100⁰C for 48h. Purification via chromatography afforded the title compound as a pale yellow solid. δH 3.30 (3H, s), 3.62 (2H, t), 4.18 (2H, t), 5.99 (IH, dd), 6.89 (IH, d), (7.27 (IH, s), 7.57 (2H, d), 7.69 (2H, m), 8.09 (IH, s), 8.16 (IH, s), 8.18 (IH, s) and 9.67 (IH, s). MH+ 402.13.

[276] A mixture of trifluoromethanesulfonic acid 1 -(2-methoxy-ethyl)-2-oxo- 1 ,2- dihydro-pyridin-4-yl ester (0.5g, 1.66mmol), bis-(pinacolato)di-boron (0.464g, 1.83mmol), potassium acetate (0.488g, 4.98mmol), PdC12(dppf) (0.04g, 0.05mmol), dppf (0.028g) in dioxane was heated at 80⁰C for 24h. The mixture was cooled, diluted with water (15mL) and extracted with ethyl acetate (3 x 5mL). The aqueous layer was concentrated and purification via elution through a silica plug afforded l-(2-methoxy-ethyl)-2-oxo-l,2-dihydro-pyridine-4- boronic acid. MH+ 198.03.

[277] A round bottom flask was charged with 4-hydroxy-l-(2-methoxy-ethyl)-lH- pyridin-2-one (5.39mmol), DCM (15mL) and triethylamine (ImL, 7mmol) and cooled to - 78°C. Triflic anhydride (ImL, 7mmol) was added drop-wise, and after stirring for a further 20min the cooling bath was removed and the mixture allowed to reach rt. After 1.5h, the mixture was diluted with further DCM, washed with aqueous saturated sodium hydrogen carbonate solution, brine, dried and concentrated. Purification via flash chromatography afforded trifluoromethanesulfonic acid l-(2-methoxy-ethyl)-2-oxo-l,2-dihydro-pyridin-4-yl ester (l.lg) as a colourless oil. MH⁺ 301.98.

[278] A mixture of 4-benzyloxy-l-(2-methoxy-ethyl)-lH-pyridin-2-one (1.4g) and

10% palladium on carbon (lOOmg) was stirred in ethyl acetate (5OmL) under a hydrogen atmosphere for 17h. Then, the mixture was filtered through celite and concentrated to afford 4-hydroxy-l-(2-methoxy-ethyl)-lH-pyridin-2-one as a colourless solid, δπ (300MHz, CH3OD) 3.67 (2H, t), 4.10 (2H, t), 4.86 (3H, s), 5.85 (IH, d), 6.04 (IH, dd) and 7.48 (IH, d). [279] To a mixture of 4-ben2yloxy-2(lH)-pyridine (2g, 9.94mmol) and caesium carbonate (6.5g, 19.88mmol) in DMF (2OmL) was added 2-bromoethyl methyl ether (1.4mL, 14.91mmol). After stirring for 17h the mixture was poured into water and extracted with ethyl acetate. The combined organics were washed with brine, dried and concentrated. Purification via flash chromatography afforded 4-benzyloxy-l-(2-methoxy-ethyl)-lH-pyridin- 2-one. MH⁺ 201.96.

[280] EXAMPLE 78: 4-[4-(Quinolin-6-yloxy)-7H-pyrrolo[2,3-^pyrimidin-6- yl]-3,6-dihydro-2J3-pyridine-l-carboxylic acid tert-butyl ester.

[281] To a stirred suspension of sodium hydride (60% dispersion in mineral oil)

(24mg, O.όmmol) in anhydrous DMSO (4mL) under argon, was added 6-hydroxyquinoline (239mg, 1.65mmol). The mixture was allowed to stir at rt for Ih. To this mixture was added l-[6-(l4ert-butoxycarbonyl-l,2,3,64etrahydropyridin-4-yl)-7H-pyrrolo[2,3-d]pyrimidin-4- yl]-4-aza-l-azonia-bicyclo[2.2.2]octane chloride (lOOmg, 0.3mmol) in DMSO (0.3mL), and the mixture stirred for a further 16h. TLC analysis showed no starting material so the mixture was neutralised with glacial acetic acid and basified with saturated aqueous sodium bicarbonate solution. The product was extracted in to EtOAc (3 x 5OmL), the organics dried with MgSO₄, filtered and concentrated under reduced pressure. The resulting residue was purified on silica gel by elution with iso-hexane: ethyl acetate to yield the title compound. IH NMR (DMSO, 400MHz) 1.4 (9H, s), 2.5 (2H, broad), 3.6 (2H, broad), 4.1 (2H, broad), 6.5 (IH, m), 6.7 (IH, s), 7.6 (IH, m), 7.7 (IH, d), 7.9 (IH, s), 8.1 (IH, d), 8.3 (IH, s), 8.4 (IH, d), 8.9 (IH, s), 12.4 (NH, s). MH⁺ = 444.24

[282] l~[6-(l-fer^Butoxycarbonyl-l,2,3,6-tetrahydropyridin-4-yl)-7iϊ- pyrrolo[2,3-rf]pyrimidin-4-yl]-4-aza-l-azoniabicyclo[2.2.2]octane chloride.

[283] To a stirred solution of IM tert-butyl 4-(4-chloro-7H-pyrrolo[2,3-<i]- pyrimidin-6-yl)-3,6-dihydropyridine-l(2H)-carboxylate (200mg, 0.6mmol) in anhydrous DMSO (0.6mL), was added l,4-Diaza-bicyclo[2.2.2]octane (370mg, 3.3mmol). The mixture was stirred under argon at rt until TLC analysis showed no starting material was present. The resulting solution containing the title compound was used directly in the next step. [284] EXAMPLE 79: Benzothiazol-6-yl-[6-(l,2,3,6-tetrahydropyridin-4-yl)-

7i/-pyrrolo [2,3-rf] pyrimidin-4-yl] amine trihydrochloride.

[285] To a suspension of benzothiazol-6-yl-(6-iodo-7H-pyrrolo[2,3-rf]pyrimidin-4- yl)-amine (4.05g, 10.3mmol) in 1 ,2-dimethoxyethane (125mL) and water (25mL) were added 4-(4,4,5,5-tetramethyl-[l,3,2]dioxaborolan-2-yl)-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester (3.5Og, 11.3mmol), [l,l'-bis(diphenylphosphino)ferrocene]dichloro palladium(II), complex with dichloromethane (1:1) (420mg, 0.51mmol) and potassium carbonate (2.85g, 20.6mmol). The flask was evacuated and refilled with N₂ (3x). The mixture was heated at 80°C overnight. The reaction mixture was diluted with EtOAc (20OmL) and water (5OmL) and filtered through a pad of celite. The organic phase was separated, and the aqueous phase was extracted with EtOAc (2 x 5OmL). The combined organic phases were washed with brine (10OmL), and dried over anhydrous sodium sulfate. Evaporation under reduced pressure afforded a brown solid. To a suspension of this crude material in methylene chloride (3OmL) was added 4M HCl/l,4-dioxane (3OmL), and the resulting mixture was stirred at rt overnight. The mixture was diluted with CH₂Cl₂ (3OmL), and the light-yellow solid was collected by filtration and dried in vacuo to give the title compound. LC-MS (ES, Pos.): 349 [MH⁺]. ¹H NMR (DMSO-d₆, 400 MHz): δ = 2.51 (m, 2H), 3.34 (m, 2H), 3.81 (m, 2H), 6.52 (s, IH), 7.09 (s, IH), 7.73 (dd, J= 8.7 Hz, 2.0 Hz, IH), 8.22 (d, J= 8.7 Hz, IH), 8.36 (d, J= 2.0 Hz, IH), 8.51 (s, IH), 9.46 (s, IH). [286] Alternative preparation: A mixture of 4-(4-chloro-7H-pyrrolo[2,3- d]pyrimidin-6-yl)-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester (5.02g, 15mmol) and l,3-benzothiazol-6-amine (2.25g, 15mmol) in 1-butanol (5OmL) was heated at 115°C overnight, LC-MS showed the desired product and some de-Boc product. After the mixture was cooled to rt, it was diluted with hexane (5OmL), the gray solid was collected by filtration, a mixture of the desired product and some de-Boc product, which was directly used in the next step. To a suspension of this material in methylene chloride (3OmL) was added 4M ΗC1/1 ,4-dioxane (3OmL), the resulting mixture was stirred at rt for 5h. The mixture was then diluted with CH₂Cl₂ (3OmL), and the light-yellow solid was collected by filtration and dried in vacuo.

[287] EXAMPLE 80: 3-{4-[4-(Benzothiazol-6-yIamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carbonyl}-benzoic acid methyl ester.

[288] The title compound was obtained following the Preferred method with Acid

Chlorides, Chloroformates, Carbamoyl Chlorides, Sulfamoyl chlorides, Sulfonyl chlorides & Isocyanates, using benzothiazol-6-yl-[6-(l,2,3,6-tetrahydropyridin-4-yl)-7H-pyrrolo[2,3- </|pyrimidin-4-yl] amine trihydrochloride and isophthalic acid monomethyl ester. ¹H NMR (DMSO, 400 MHz): δ = 9.6(lH,s), 9.25(lH,s), 8.9(lH,s), 8.3(lH,s), 8.1-8.0(3H,m), 7.9(lH,d), 7.75 (IH, d), 7.65(1H, t), 6.85(1H, s), 6.5(1H, m), 6.3(1H, m), 4.3(1H, m), 4.1(1H, m), 3.9(3H, s), 3.6(1H, m), 2.6(1H, m). [MH⁺ - CH₃] = 512.45.

[289] EXAMPLE 81: 3-{4-[4-(Benzothiazol-6-yIamino)-7H-pyrroIo[2,3-rf]- pyriniidin-δ-yll-Sjβ-diliydro^H-pyridine-l-carbonylJ-benzoic acid.

[290] 344-[4<Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-rf]pyrimidin-6-yl]-3,6- dihydro-2H-pyridine-l-carbonyl} -benzoic acid methyl ester (0.624mniol) was suspended in a mixture of MeOH (6.OmL) and water (2.OmL). 2M NaOH solution (1.Ommol) was then added to the above suspension and the reaction temperature increased to 65°C. The resulting suspension was stirred for a further period of 16h. The mixture was allowed to reach r.t and diluted with EtOAc (3OmL) and washed with 2M NaOH (2x20mL). The aqueous phase was then acidified by careful addition of cone. HCl solution until pH∞l . The resulting brown precipitate was then filtered and dried under vacuum affording the title compound. ¹H NMR (DMSO, 400 MHz): δ = 9.45(lH,s), 8.7(lH,s), 8.15(lH,d), 8.1(lH,d), 8.0(lH,s), 7.8(lH,d), 7.7 (IH, d), 7.6(1H, t), 6.9(1H, s), 6.6(1H, m), 6.35(1H, m), 4.35(1H, m), 4.1(1H, m), 3.9(1H, m), 2.6(1H, m). [MH⁺ - CO₂] = 498.25.

[291] EXAMPLE 82: l-{4-[4-(lH-Indazol-5-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yl}-2-phenylethanone.

[292] To a solution of (lH-indazol-5-yl)-[6-(l ,2,3 ,6-tetrahydropyridin-4-yl)-7H- pyrrolo[2,3-rf]pyrimidin-4-yl]amine tri-hydrochloride (73.6mg, 0.2mmol) and phenylacetyl chloride (31mg, 0.2mmol) in dichloromethane (1.5mL) was added Z-Pr₂NEt (O.lmL). The resulting mixture was stirred at rt for 3h. MeOH (0.3mL) was added to quench the reaction. Solvents were removed and the residue was dissolved in DMF («2mL), which was purified by mass-directed ΗPLC to obtain the title compound. ¹H-NMR (DMSO-d₆, 400 MHz): δ = 2.34 (m, 2 H), 3.72 (t, J= 5.6 Hz, 2 H), 3.80 (d, J= 17.6 Hz, 2 H), 4.21 (d, J= 35.6 Hz, 2 H), 6.40 (s, 1 H), 6.73 (d₃ J= 38.4 Hz, 1 H), 7.22-7.34 (m, 4 H), 7.51 (d, J= 8.8 Hz, 1 H), 7.63 (m, 1 H), 8.04 (s, 1 H), 8.25 (d, J= 4.4 Hz, 1 H), 8.37 (t, J= 12 Hz, 1 H), 9.33 (d, J= 13.6 Hz, 1 H), 11.92 (d, /= 14.8 Hz, 1 H), 12.97 (s, 1 H). MS (ES+): m/z 450.07 [MH⁺]. HPLC: t_κ = 2.17 min (ZQ2000, polar_5min).

[293] EXAMPLE 83: Phenyl 4-[4-(lH-indazol-5-ylamino)-7H-pyrrolo [2,3- rf)pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylate.

[294] The title compound was obtained following the Preferred method with Acid

Chlorides, Chloroformates, Carbamoyl Chlorides, Sulfamoyl chlorides, Sulfonyl chlorides & Isocyanates, using phenyl chloroformate. ¹H-NMR (DMSO-d₆, 400 MHz): δ = 2.58-2.62 (m, 2 H), 3.70 (m, 1 H), 3.84 (m, 1 H), 4.16 (m, 1 H), 4.35 (m, 1 H), 6.45 (s, 1 H), 6.81 (s, 1 H), 7.17 (d, J= 8.4 Hz, 2 H), 7.23 (X, J= 6.8 Hz, 1 H), 7.40 (t, J= 7.2 Hz, 2 H), 7.52 (d, J= 8.8 Hz, 1 H), 7.66 (d, J= 12 Hz, 1 H), 8.05 (s, 1 H), 8.26 (s, 1 H), 8.38 (s, 1 H), 9.36 (s, 1 H), 11.97 (s, 1 H), 12.97 (s, 1 H). MS (ES+): m/z 452.02 [MH⁺]. HPLC: fo = 2.38 min (ZQ2000, polar_5min).

[295] EXAMPLE 84: iV-Methyl-iV-phenyI4-[4-(lH-indazoI-5-ylamino)-7H- pyrrolo[2,3-^pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxamide.

[296] The title compound was obtained following the Preferred method with Acid

Chlorides, Chloroformates, Carbamoyl Chlorides, Sulfamoyl chlorides, Sulfonyl chlorides & Isocyanates, using N-methyl-N-phenylcarbamoylchloride. ¹H-NMR (DMSO-d₆, 400 MHz): δ = 2.20 (m, 2 H), 3.13 (s, 3 H), 3.78 (m, 2 H), 6.28 (s, 1 H), 6.66 (s, 1 H), 7.14 (d, J= 7.2 Hz, 1 H), 7.18 (d, J= 8.4 Hz, 2 H), 7.38 (t, J= 7.2 Hz, 2 H), 7.50 (d, J= 8.8 Hz, 1 H), 7.64 (d, J= 9.2 Hz, 1 H), 8.04 (s, 1 H), 8.24 (d, J= 5.2 Hz, 1 H), 8.36 (d, J= 6.4 Hz, 1 H), 9.29 (s, 1 H), 11.85 (s, 1 H), 12.96 (s, 1 H). MS (ES+): m/z 465.04 [MH⁺]. HPLC: /_R = 2.25 min (ZQ2000, polar_5min).

[297] EXAMPLE 85: 4-[4-(lH-Indazol-5-ylamino)-7H-pyrroIo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxythioamide.

[298] The title compound was obtained following the Preferred method with Acid

Chlorides, Chloroformates, Carbamoyl Chlorides, Sulfamoyl chlorides, Sulfonyl chlorides & Isocyanates, using phenyl isothiocyanate. ¹H-NMR (DMSO-d₆, 400 MHz): δ = 2.62 (m, 2 H), 4.17 (t, J= 6.0 Hz, 2 H), 4.55 (m, 2 H), 6.44 (s, 1 H), 6.80 (s, 1 H), 7.14 (m, 1 H), 7.31-7.33 (m, 3 H), 7.52 (d, J= 8.8 Hz, 1 H), 7.66 (d, J= 8.8 Hz, 1 H), 8.05 (s, 1 H), 8.27 (d, J= 1.2

Hz, 1 H), 8.38 (d, J= 6.8 Hz, 1 H), 9.36 (s, 1 H), 11.95 (s, 1 H), 12.97 (s, 1 H). MS (ES+): m/z 467.00 [MH⁺]. HPLC: t_R = 2.33 min (ZQ2000, polar_5min).

[299] EXAMPLE 86: tert-Butyl 4-[4-(lH-indazol-5-yIamino)-7J3-pyrrolo[2,3- rf]pyrimidin-6-yI]-3,6-dihydro-2H-pyridine-l-carboxyamide.

[300] The title compound was obtained following the Preferred method with Acid

Chlorides, Chloroformates, Carbamoyl Chlorides, Sulfamoyl chlorides, Sulfonyl chlorides & Isocyanates, using tert-butyl isocyanate. ¹H-NMR (DMSOd₆, 400 MHz): δ = 1.28 (s, 9 H), 2.44 (m, 2 H), 3.52 (t, J= 4.8 Hz, 2 H), 3.99 (m, 2 H), 5.79 (s, 1 H), 6.40 (s, 1 H), 6.74 (s, 1 H), 7.52 (d, J= 8.8 Hz, 1 H), 7.66 (dd, J= 1.6, 8.8 Hz, 1 H), 8.05 (s, 1 H), 8.25 (s, 1 H), 8.37 (s, 1 H), 9.32 (s, 1 H), 11.90 (s, 1 H), 12.97 (s, 1 H). MS (ES+): m/z 431.04 [MH⁺]. HPLC: t_κ = 2.14 min (ZQ2000, polar_5min).

[301] EXAMPLE 87: Ethyl 4-[4-(lH-indazol-5-ylamino)-7H-pyrrolo [2,3- d\ pyrimidin-6-yl] -Sjό-dihydro^H-pyridine-l-carboxyamide.

[302] The title compound was obtained following the Preferred method with Acid

Chlorides, Chloroformates, Carbamoyl Chlorides, Sulfamoyl chlorides, Sulfonyl chlorides & Isocyanates, using ethyl isocyanate. ¹H-NMR (CD₃OD, 400 MHz): δ = 1.14 (t, J= 6.4 Hz, 3 H), 2.54 (m, 2 H), 3.23 (q, J= 6.8 Hz, 2 H), 3.65 (t, J= 5.2 Hz, 2 H), 4.11 (m, 2 H), 6.40 (s, 1 H), 6.68 (s, br, 1 H), 7.47 (d, J= 8.8 Hz, 1 H), 7.76 (d, J= 8.4 Hz, 1 H), 7.98 (s, 1 H), 8.12 (s, 1 H), 8.17 (s, 1 H). MS (ES+): m/z 403.05 [MH⁺]. HPLC: ^ = 1.86 min (ZQ2000, polar_5min).

[303] EXAMPLE 88: 4-[4-(lH-Indazol-5-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid (2-fluorophenyl)-amide.

[304] The title compound was obtained following the Preferred method with Acid

Chlorides, Chloroformates, Carbamoyl Chlorides, Sulfamoyl chlorides, Sulfonyl chlorides & Isocyanates, using 2-fluorophenyl isocyanate. ¹H NMR (400 MHz, DMSO-J,;): δ = 2.53- 2.59 (m, 2H), 3.70 (t, J= 5.2 Hz, 2H), 4.19 (s, br, 2H), 6.45 (s, br, IH), 6.78 (s, IH), 7.10- 7.16 (m, 2H), 7.17-7.23 (m, IH), 7.42-7.49 (m,, IH), 7.52 (d, J= 9.2 Hz, IH), 7.66 (dd, J= 8.8, 1.6 Hz, IH), 8.05 (s, IH), 8.26 (s, IH), 8.34 (s, -NH), 8.37 (s, IH), 9.33 (s, -NH), 11.93 (s, -NH), 12.96 (s, -NH). MS (ES+): m/z 469.02 (100) [MH⁺]. HPLC: t_κ = 2.16 min (ZQ2000, polar_5min).

[305] EXAMPLE 89: 4-[4-(lH-Indazol-5-ylamino)-7#-pyrroIo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2i3-pyridme-l-carboxylic acid (3-fluorophenyl)-amide.

[306] The title compound was obtained following the Preferred method with Acid

Chlorides, Chloroformates, Carbamoyl Chlorides, Sulfamoyl chlorides, Sulfonyl chlorides & Isocyanates, using 3 -fluorophenyl isocyanate. ¹H NMR (400 MHz, DMSO-Js): δ = 2.44- 2.56 (m, 2H), 3.70 (t, J= 5.6 Hz, 2H), 4.21 (s, br, 2H), 6.46 (s, br, IH), 6.70-6.80 (m, 2H), 7.22-7.32 (m, 2H), 7.44-7.55 (m, 2H), 7.65 (dd, J= 8.8, 1.6 Hz, IH), 8.05 (s, IH), 8.26 (s, IH), 8.36 (d, J= 2.0 Hz, IH), 8.75 (s, -NH), 9.33 (s, -NH), 11.92 (s, -NH), 12.96 (s, -NH). MS (ES+): 7^ 469.02 (10O) [MH⁺]. HPLC: /_R = 2.32 min (ZQ2000, polar_5rnin). [307] EXAMPLE 90: 4-[4-(lH-Indazol-5-yIamino)-7H-pyrroIo[2,3-rf]- pyπmidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid (4-fluorophenyl)-amide.

[308] The title compound was obtained following the Preferred method with Acid

Chlorides, Chloroformates, Carbamoyl Chlorides, Sulfamoyl chlorides, Sulfonyl chlorides & Isocyanates, using 4-fluorophenyl isocyanate. ¹H NMR (400 MHz, DMSO-J₁₅): δ = 2.44- 2.56 (m, 2H), 3.67-3.72 (Hi₀, 2H), 4.19 (d, J= 1.2 Hz, 2H), 6.46 (s, br, IH), 6.77 (s, IH), 7.08 (t, J= 8.8 Hz, 2H), 7.47-7.54 (m, 3H), 7.66 (dd, J= 8.8, 2.0 Hz, IH), 8.05 (s, IH), 8.26 (s, IH), 8.36 (d, J= 1.2 Hz, IH), 8.57 (s, -NH), 9.33 (s, -NH), 12.96 (s, -NH). MS (ES+): m/z 469.02 (100) [MH⁺]. HPLC: t_κ = 2.26 min (ZQ2000, polarjmin). [309] EXAMPLE 91: 4-[4-(lH-Indazol-5-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxyIic acid (2-methoxyphenyl)-amide.

[310] The title compound was obtained following the Preferred method with Acid

Chlorides, Chloroformates, Carbamoyl Chlorides, Sulfamoyl chlorides, Sulfonyl chlorides & Isocyanates, using 2-methoxyphenyl isocyanate. ¹H NMR (400 MHz, DMSO-d₆): δ = 2.53- 2.56 (m, 2H), 3.68 (t, J= 5.2 Hz, 2H), 3.83 (s, 3H), 4.19 (s, br, 2H), 6.44 (s, br, IH), 6.78 (s, IH), 6.85-6.95 (m,, IH), 6.99-7.04 (m, 2H), 7.52 (d, J= 9.2 Hz, IH), 7.64-7.68 (m, 2H), 7.70 (s, -NH), 8.05 (s, IH), 8.26 (s, IH), 8.37 (s, IH), 9.34 (s, -NH)₅ 11.94 (s, -NH), 12.97 (S₅ -NH). MS (ES+): m/z 481.03 (100) [MH⁺]. HPLC: t_R = 2.23 min (ZQ2000, polar_5min).

[311] EXAMPLE 92: 4-[4-(lH-Indazol-5-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid (3-methoxyphenyl)-amide.

[312] The title compound was obtained following the Preferred method with Acid

Chlorides, Chloroformates, Carbamoyl Chlorides, Sulfamoyl chlorides, Sulfonyl chlorides & Isocyanates, using 3-methoxyphenyl isocyanate. ¹H NMR (400 MHz, DMSO-^): δ = 2.43- 2.47 (m, 2H)₅ 3.67-3.70 (m₅ 2H), 3.71 (s, 3H), 4.19 (s, br, 2H), 6.46 (s, br, IH), 6.52 (ddd, J= 7.6, 2.4, 1.6 Hz, IH), 6.77 (s, IH), 7.07-7.12 (m, IH)₅ 7.14 (dd, J= 8.0, 7.6 Hz₅ IH), 7.19 (t, J= 2.0 Hz₅ IH), 7.52 (d₅ J= 8.8 Hz, IH), 7.66 (dd, J= 8.8, 1.6 Hz, IH), 8.05 (s, IH), 8.26 (s, IH), 8.37 (s, IH), 8.53 (s, -NH), 9.33 (s, -NH), 11.92 (s, -NH), 12.97 (s, -NH). MS (ES+): m/z 481.03 (100) [MH⁺]. HPLC: t_R = 2.23 min (ZQ2000, polar5min). [313] EXAMPLE 93: 4-[4-(lH-Indazol-S-ylamino)-7H-pyrrolo[2,3-rf[- pyrimidin-6-yI]-3,6-dihydro-2H-pyridine-l-carboxylic acid (4-methoxyphenyl)-amide.

[314] The title compound was obtained following the Preferred method with Acid

Chlorides, Chloroformates, Carbamoyl Chlorides, Sulfamoyl chlorides, Sulfonyl chlorides & Isocyanates, using 4-methoxyphenyl isocyanate. ¹H NMR (400 MHz, MeOH-J^): δ = 2.61 (s, br, 2H), 3.75-3.80 (m, 2H), 3.77 (s, 3H), 4.26 (s, br, 2H), 6.44 (s, br, IH), 6.63-6.78 (s, br, IH), 6.86 (dd, J= 6.8, 2.0 Hz, 2H), 7.25 (dd, J= 6.8, 2.0 Hz, 2H), 7.48 (dd, J= 8.8, 2.4 Hz, IH), 7.77 (d, J= 8.8 Hz, IH), 7.98 (d, J= 2.4 Hz, IH), 8.13 (s, IH), 8.18 (s, IH). MS (ES+): m/z 480.97 (100) [MH⁺]. HPLC: t_R = 2.13 min (ZQ2000, polar_5min). [315] EXAMPLE 94: 4-[4-(lH-Indazol-5-yIamino)-7H-pyrrolo[2,3-rf]- pyrimidm-6-yl]-3,6-dihydro-2i2-pyridine-l-carboxylic acid phenylamide.

[316] The title compound was obtained following the Preferred method with Acid

Chlorides, Chloroformates, Carbamoyl Chlorides, Sulfamoyl chlorides, Sulfonyl chlorides & Isocyanates, using phenyl isocyanate. ¹H NMR (400 MHz, DMSO-J₁₅): δ = 2.43-2.57 (m, 2H), 3.69 (m, 2H), 4.21 (s, br, 2H), 6.51 (s, br, IH), 6.75-6.84 (s, br, IH), 6.95 (t, J= 7.2 Hz, IH), 7.24 (t, J= 8.8 Hz, 2H), 7.49 (d, J= 7.6 Hz, 2H), 7.51-7.57 (s, br, IH), 7.60-7.67 (s, br, IH), 8.08-8.20 (m, br, IH + -NH), 8.25 (s, IH), 8.55 (s, IH), 13.01-13.31 (s, br, -NH). MS (ES+): m/z 451.01 (100) [MH⁺]. HPLC: ^ = 2.21 min (ZQ2000, polar_5min). [317] EXAMPLE 95: 4-[4-(lH-IndazoI-5-ylamino)-7H-pyrroIo[2,3-<fl- pyrimidin-6-yI] -3 ,6-dihydro-2£T-pyridine-l-carboxyIic acid benzylamide.

[318] The title compound was obtained following the Preferred method with Acid

Chlorides, Chloroformates, Carbamoyl Chlorides, Sulfamoyl chlorides, Sulfonyl chlorides & Isocyanates, using benzyl isocyanate. ¹H NMR (400 MHz, DMSO-J₅): δ = 2.44-2.53 (m, 2H), 3.60 (t, J= 5.2 Hz, 2H), 4.07 (s, br, 2H), 4.28 (d, J= 5.6 Hz, 2H), 6.42 (s, br, IH), 6.75 (s, IH), 7.14 (t, J= 5.6 Hz, -NH), 7.18-7.23 (m, IH), 7.25-7.34 (m, 4H), 7.51 (d, J= 8.8 Hz, IH), 7.65 (dd, J= 9.2, 2.0 Hz, IH), 8.04 (s, IH), 8.25 (s, IH), 8.36 (d, J= 0.8 Hz, IH), 9.31 (s, -NH), 11.88 (s, -NH), 12.96 (s, -NH). MS (ES+): m/z 465.04 (100) [MH⁺]. HPLC: *_R = 2.20 min (ZQ2000, polar_5min).

[319] EXAMPLE 96: 4-[4-(lH-IndazoI-5-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxyIic acid amide.

[320] The title compound was obtained following the Preferred method with Acid

Chlorides, Chloroformates, Carbamoyl Chlorides, Sulfamoyl chlorides, Sulfonyl chlorides & Isocyanates, using trimethylsilyl isocyanate. ¹H NMR (400 MHz, DMSO-J₁₅): δ = 2.33 (s, br, 2H), 3.53 (t, J= 5.6 Hz, 2H), 4.00 (d, J= 2.4 Hz, 2H), 6.03 (s, -NH₂), 6.39 (s, br, IH), 6.75 (s, IH), 7.51 (d, J= 9.2 Hz, IH), 7.65 (dd, J= 8.8, 2.0 Hz, IH), 8.04 (s, IH), 8.25 (s, IH), 8.36 (d, J= 1.6 Hz, IH), 9.30 (s, -NH), 11.88 (s,-NH), 12.96 (s, -NH). MS (ES+): m/z 375.13 (100) [MH⁺]. HPLC: t_R = 1.76 min (ZQ2000, polar_5min). [321] EXAMPLE 97: 4-[4-(lH-Indazol-5-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yI]-3,6-dihydro-2fi-pyridine-l-carboxyIic acid pyridin-3-yIamide.

[322] The title compound was obtained following the Preferred method with Acid

Chlorides, Chloroformates, Carbamoyl Chlorides, Sulfamoyl chlorides, Sulfonyl chlorides & Isocyanates, using 3-pyridyl isocyanate. ¹H NMR (400 MHz, DMSO-J₁₅): δ = 2.48-2.57 (m, 2H), 3.75 (t, J= 5.6 Hz, 2H), 4.27 (s, br, 2H), 6.54 (s, br, IH), 6.79 (s, br, IH), 7.50 (dd, J= 8.8, 1.6 Hz, IH), 7.67 (d, J= 8.8 Hz, IH), 7.76 (dd, J= 8.8, 5.6 Hz, IH), 8.08-8.13 (m, IH), 8.15 (d, J= 0.4 Hz, IH), 8.26 (s, IH), 8.30-8.37 (m, IH), 8.41 (d, J= 4.4 Hz, IH), 8.99 (d, J = 2.4 Hz, IH), 9.33 (s, -NH), 10.87 (s, br, -NH), 12.68 (s, br, -NH), 13.06 (s, br, -NH). MS (ES+): m/z 452.02 (10) [MH⁺]. HPLC: t_R = 1.75 min (ZQ2000, polar_5min). [323] EXAMPLE 98: 2-PyridinyI 4-[4-(lH-indazol-5-yIamino)-7H-pyrrolo-

[2,3-rf] pyriraidin-6-yl] -Sjό-dihydro-ΣH-pyridine-l-carboxyamide.

[324] A solution of 2-aminopyridine (22.6mg, 0.24mmol) and diimidazol-1- ylmethanone (CDI, 39mg, 0.24mmol) in DMF (0.75mL) was stirred at 5O⁰C for Ih. After cooling to rt, Z-Pr₂NEt (0.14mL, 0.8mmol) was added, followed by (lH-indazol-5-yl)-[6- (1 ,2,3 ,6-tetrahydropyridin-4-yl)-7H-pyrrolo[2,3- J]pyrimidin-4-yl] amine tri-ΗCl (88. lmg, 0.2mmol). The mixture was stirred at rt for 2h and 5O⁰C for 3h. The resulting mixture was filtered and submitted to mass-directed ΗPLC purification to yield the title compound. ¹H- NMR(CD₃OD, 400 MHz): δ = 2.66 (m, 2 H), 3.88 (t, J= 6.0 Hz, 2 H), 4.37 (m, 2 H), 6.45 (s, 1 H), 6.71 (s, br, 1 H), 7.38 (t, J= 6.0 Hz, 1 H), 7.48 (dd, J= 2.0, 9.2 Hz, 1 H), 7.66 (d, J= 8.8 Hz, 1 H), 7.76 (d, J= 8.8 Hz, 1 H), 7.98 (d, J= 1.2 Hz, 1 H), 8.16 (d, J= 12.4 Hz, 1 H), 8.22 (dt, J= 1.6, 8.8 Hz, 1 H). 8.29 (d, J= 6.0 Hz, 1 H). MS (ES+): m/z 451.95 [MH⁺]. ^'

HPLC: t_κ = 1.77 min (ZQ2000, polar_5min).

[325] EXAMPLE 99: 4-Pyridinyl 4-[4-(l#-indazol-5-ylamino)-7fi-pyrroIo-

[2,3-rf]pyrimidin-6-yl]-3,6-dihydro-2fl-pyridine-l-carboxyamide.

[326] The title compound was prepared following the procedure for the corresponding 2-pyridyl compound, but using 4-aminopyridine. 'H-NMRtDMSO-d_δ, 400 MHz): δ = 3.72 (t, J= 6.4 Hz, 2 H), 4.22 (m, 2 H), 6.46 (s, 1 H), 6.68 (s, br, 1 H), 6.78 (s, 1 H), 7.51-7.53 (m, 2 H), 7.55 (dd, J= 1.6, 8.8 Hz, 1 H), 8.05 (s, 1 H), 8.26 (d, J= 2.0 Hz, 1 H), 8.30-8.33 (m, 2 H), 8.36 (s, 1 H), 8.99 (s, 1 H), 9.34 (s, 1 H), 11.94 (s, 1 H), 12.97 (s, 1 H). MS (ES+): m/z 452.02 [MH⁺]. HPLC: t_R = 1.62 min (ZQ2000, polar_5min). [327] EXAMPLE 100: l-{4-[4-(Benzothiazol-6-yIamino)-7H-pyrrolo[2,3-rfl- pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yI}-2-pyridin-3-ylethanone.

[328] To a suspension of benzothiazol-6-yl-[6-(l,2,3,6-tetrahydropyridin-4-yl)-7H-

P3ττolo[2,3-d]pyrimidin-4-yl]amine tri-ΗCl (137mg, 0.300mmol), 3-pyridinylacetic acid-ΗCl (78.1mg, 0.450mmol), and EDC (115mg, O.όOOmmol) in DMF (ImL) was added N,N- diisopropylethylamine (0.26ImL, 1.50mmol). The mixture became a clear solution after being stirred for a few minutes and was stirred overnight. The products, which precipitated from the solution during the reaction, were collected by filtration, washed with dichloromethane (2xlmL), and dried in vacuo to afford the title compound as a white solid. ¹H-NMR (DMSO-d₆₅400 MHz): δ = 2.73 (s, 2 H), 2.89 (s, 2 H), 3.78 (dt, J= 4.0, 18.8 Hz, 2 H), 3.86 (d, J= 20 Hz, 2 H), 4.19 (s, 1 H), 4.33 (s, 1 H), 6.45 (d, J= 5.2 Hz, 1 H), 6.84 (d, J= 16.8 Hz, 1 H), 7.33-7.36 (m, 1 H), 7.65 (t, J= 8.0 Hz, 1 H), 7.87 (dt, J= 2.0, 8.0 Hz, 1 H), 7.95 (s, 1 H), 8.04 (d, J= 9.2 Hz, 1 H), 8.34 (d, J= 3.6 Hz, 1 H), 8.44-8.48 (m, 1 H), 8.92 (s, 1 H), 9.24 (s, 1 H), 9.62 (d, J= 7.6 Hz, 1 H). MS (ES+): m/z 467.94 [MH⁺]. HPLC: t_κ = 1.98 min (ZQ2000, polar_5min).

[329] EXAMPLE 101: 4-(4-(l,3-Benzothiazol-6-ylamino)-7J2-pyrroIo[2,3-rf]- pyrimidin-6-yl)-Λ'-(4-fluorophenyl)-3,6-dihydropyridine-l(2H)-carboxamide.

[330] To a suspension of benzothiazol-6-yl-[6-(l,2,3,6-tetrahydropyiidin-4-yl)-7/f- pyrrolo[2,3-rf]pyrimidin-4-yl] amine trihydrochloride (50.0mg, O.llmmol) in DMF (1.5mL) was added N^V-diisopropylethylamine (0.04mL, 0.20mmol). The reaction mixture stirred at - 2O⁰C for 5 min prior to the addition of 4-fluorophenyl isocyanate (9.5mg, 0.07mmol) in DMF (0.5mL). The mixture was left to stir at rt for Ih. The mixture was concentrated in vacuo and purified via MDP, which afforded the title compound as a white solid. MS (ES+): m/z: 485.88 (100) [MH⁺]. HPLC: U = 2.73 min (ZQ2000: polar_5 min). ¹H ΝMR (400 MHz, CDCl₃): δ = 2.52 - 2.56 (m, 2H), 3.31 (s, IH), 3.70 (t, 2H), 4.20 (s, 2H), 6.94 (m, IH), 6.86 (d, J= 0.8 Hz, IH), 7.06 - 7.11 (m, 2H), 7.48 - 7.51 (m, 2H), 7.87 (dd, J= 2.4, 8.8 Hz, IH), 8.04 (d, J= 8.8 Hz, IH), 8.35 (s, IH), 8.59 (s, IH), 8.92 (d, J= 2.0 Hz, IH), 9.24 (s, IH), 9.62 (s, IH).

[331] EXAMPLE 102: 4-(4-(l,3-BenzothiazoI-6-ylamino)-7J3-pyrrolo[2,3-rf]- pyrimidin-6-yI)-iV-(2-fluorophenyl)-3,6-dihydropyridine-l(2_J£i^r)-carboxamide.

[332] The procedure for EXAMPLE 101 was followed except for replacing 4- fluorophenyl isocyanate with 2-fluorophenyl isocyanate. ¹H ΝMR (400 MHz, DMSO-^₅): δ = 2.57 (s, br, 2H), 3.71 (t, J= 5.2 Hz, 2H), 4.21 (s, br, 2H), 6.49 (s, br, IH), 6.87 (d, J= 2.0 Hz, IH), 7.10-7.16 (m, 2H), 7.17-7.23 (m, IH), 7.42-7.49 (m,, IH), 7.88 (dd, J= 8.8, 2.0 Hz, IH), 8.04 (d, J= 8.8 Hz, IH), 8.34 (s, br, -NH), 8.35 (s, IH), 8.92 (d, J= 2.0 Hz₅ IH), 9.24 (s, IH), 9.61 (s, -NH), 12.03 (s, -NH). MS (ES+): 485.98 (100) [MH⁺]. HPLC: /_R = 2.69 min (ZQ2000, polar_5min).

[333] EXAMPLE 103: 4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-//]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxyIic acid phenylamide.

[334] The procedure for EXAMPLE 101 was followed except for replacing 4- fluorophenyl isocyanate with phenyl isocyanate. ¹H NMR (400 MHz, DMSO-Gk): δ = 2.57 (s, br, 2H), 3.71 (t, J= 5.2 Hz, 2H), 4.21 (d, J= 1.6 Hz, 2H), 6.49 (s, br, IH), 6.86 (d, J= 2.0 Hz, IH), 6.95 (m_e, IH), 7.24 (rr^, 2H), 7.49 (dd, J= 8.8, 1.2 Hz, 2H), 7.88 (dd, J= 8.8, 2.4 Hz, IH), 8.04 (d, J= 8.8 Hz, IH), 8.35 (s, IH), 8.54 (s, -NH), 8.92 (d, J= 2.4 Hz, IH), 9.24 (s, IH), 9.61 (s, -NH), 12.03 (d, J= 2.0 Hz, -NH). MS (ES+): m/z 468.01 (100) [MH⁺]. HPLC: fe = 2.70 min (ZQ2000, polar_5min).

[335] EXAMPLE 104: 4-[4-(BenzothiazoI-6-yIamino)-7H-pyrroIo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxyIic acid amide.

[336] The procedure for EXAMPLE 101 was followed except for replacing 4- fluorophenyl isocyanate with trimethylsilyl isocyanate. ¹H NMR (400 MHz, DMSO-J₁;): δ = 2.42-2.52 (m, 2H), 3.55 (t, J= 5.6 Hz, 2H), 4.02 (d, J= 2.0 Hz, 2H), 6.04 (s, -NH₂), 6.43 (s, br, IH), 6.83 (d, J= 2.0 Hz₅ IH)₅ 7.88 (dd, J= 8.8, 2.4 Hz₅ IH)₅ 8.04 (d, J= 8.8 Hz, IH), 8.34 (s, IH)₅ 8.92 (d, J= 2.4 Hz₅ IH)₅ 9.23 (s, IH)₅ 9.59 (s, -NH), 11.99 (s, -NH). MS (ES+): m/z 392.06 (100) [MH⁺]. HPLC: t_R = 2.10 min (ZQ2000, polar_5min). [337] EXAMPLE 105: 4-[4-(BenzothiazoI-6-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butylamide.

[338] The procedure for EXAMPLE 101 was followed except for replacing 4- fluorophenyl isocyanate with /er/-butyl isocyanate. Workup was carried out as follows: Residue was triturated in hot MeOH and was filtered. No solid was obtained but filtrate instantly precipitated. This off-white solid was filtered and again the filtrate was concentrated in vacuo, resuspended in MeOH₅ and filtered again (3x), until solid no longer precipitated from filtrate. Solid afforded the title compound, as an off-white solid. Mass directed purification (MDPS) of filtrate yielded a second batch of the title compound, as an off-white solid. ¹H NMR (400 MHz, DMSO-rf_β): 1.28 (s, 9H), 2.43-2.56 (m, 2H)₅3.53 (t, J= 5.6 Hz, 2H), 3.99 (d, J= 2.0 Hz, 2H)₅ 5.79 (s, -NH), 6.43 (s, br, IH), 6.82 (d, J= 1.2 Hz, IH)₅ 7.88 (dd, J= 8.8, 2.0 Hz₅ IH)₅ 8.04 (d, J= 8.8 Hz, IH), 8.34 (s, IH)₅ 8.92 (d, J= 2.0 Hz₅ IH) 9.23 (s, IH), 9.59 (s, -NH)₅ 11.99 (S₅ -NH). MS (ES+): m/z 448.04 (100) [MH⁺]. HPLC: t_R = 2.63 min (ZQ2000, polar_5min).

[339] EXAMPLE 106: 4-[4-(BenzothiazoI-6-yIamino)-7H-pyrroIo[2,3-d]- pyrimidin-6-yl] -3,6-dihydro-2H-pyridine-l-carboxylic acid isopropylamide.

[340] The procedure for EXAMPLE 101 was followed except for replacing 4- fluorophenyl isocyanate with isopropyl isocyanate. For purification, no chromatography was performed; material was triturated twice in MeOH to obtain the title compound as orange solid. ¹H NMR (400 MHz, DMSO-J₆): δ = 1.01 (d, J= 6.8 Hz, 6H), 2.37-2.45 (m, 2H), 3.49 (t, J= 5.6 Hz, 2H), 3.73 (dsept, J= 6.8, 6.8 Hz, IH), 3.94 (d, J= 1.6 Hz, 2H), 6.20 (d, J= 7.6 Hz, IH), 6.44 (s, br, IH), 6.83 (d, J= 1.6 Hz, IH), 7.88 (dd, J= 8.8, 2.0 Hz, IH), 8.04 (d, J= 8.8 Hz, IH), 8.34 (s, IH), 8.92 (d, J= 2.0 Hz, IH), 9.23 (s, IH), 9.58 (s, -NH), 11.98 (s, - NH). MS (ES+): m/z 434.04 (100) [MH⁺]. HPLC: fe = 2.43 min (ZQ2000, polar_5min). [341] EXAMPLE 107: 4-(4-(l,3-BenzothiazoI-6-ylamino)-7fi-pyrrolo[2,3-rf|- pyrimidin-6-yl)methylpiperazinyI-3,6-dihydropyridine-l(2H)-yI)-carboxamide.

[342] To a suspension of benzothiazol-6-yl-[6-(l ,2,3,6-tetrahydropyridin-4-yl)-7H- pyrrolo[2,3-J]pyrimidin-4-yl]-amine tris-hydrochloride (200mg, 0.44mmol) in NJSf- dimethylformamide (6mL) was added N,N-diisopropylethylamine (0.5mL, 3mmol). The reaction mixture was stirred at O⁰C for 5min prior to the addition of 4-methylpiperazine-l- carbonyl chloride hydrochloride (87mg, 0.44mmol). The resulting mixture was stirred at 0⁰C for Ih, diluted with water (5OmL), and the resulting precipitate was collected by filtration, washed with EtOAc (5mL), and dried in vacuo to give the title compound. LC-MS (ES, Pos.): 474 [MH⁺], and ¹H ΝMR (DMSO-d₆, 400 MHz): δ = 1.99 (s, 3H), 2.24 (m, 4H), 2.50 (m, 2H), 3.18 (m, 4H), 3.41 (m, 2H), 3.93 (m, 2H), 6.41 (s, IH), 6.82 (s, IH), 7.87 (d, J= 8.8 Hz, IH), 8.04 (d, J= 8.8 Hz, IH), 8.34 (s, IH), 8.91 (s, IH), 9.23 (s, IH), 9.59 (s, IH), 11.99 (s, IH).

[343] EXAMPLE 108: 4-(4-(l,3-Benzothiazol-6-yIamino)-7H-pyrroIo[2,3-rf]- pyrimidin-6-yl)-ΛVV-dimethyl-3,6-dihydropyridine-l(2H)-carboxamide.

[344] The procedure for EXAMPLE 101 was followed except for replacing 4- fluorophenyl isocyanate with N,N-dmiethylcarbamoyl chloride. MS (ES+): m/z: 419.98 (100) [MH⁺]. HPLC: t_x = 2.35 min (ZQ2000: polar_5 min). ¹H NMR (400 MHz, DMSO-d₆): δ =

2.77 (s, 6H), 3.31 - 3.39 (m, 4H), 3.89 (d, J= 2.4 Hz, 2H), 6.42 (s, IH), 6.82 (d, J= 2.0 Hz,

IH), 7.86 - 7.89 (dd, J= 2.0, 9.2 Hz, IH), 8.03 (d, J= 9.2 Hz, IH), 8.34 (s, IH), 8.91 (d, J=

2.0 Hz, IH), 9.23 (s, IH), 9.60 (s, IH).

[345] EXAMPLE 109: 6-{l-[4-(Dimethylamino)butanoyI]-l,2,3,6-tetra- hydropyridin-4-yI}-N-l,3-benzothiazol-6-yI-7J?-pyrrolo[2,3-rf]pyrimidin-4-amine.

[346] To a solution of benzothiazol-6-yl-[6-(l,2,3,6-tetrahydropyridin-4-yl)-7H- pyrrolo[2,3-d]pyrimidin-4-yl]-amine trihydrochloride (50.0mg, 0.1 lmmol) in DMF (3mL) was added 4-(dimethylamino)butyric acid hydrochloride (17mg, 0.13mmol), TBTU (42mg, 0.13mmol) and N^V-diisopropylethylamine (0.ImL). The reaction mixture was left to stir at rt over the weekend. The crude mixture was concentrated in vacuo and purified via MDP, which afforded the title compound as a tan solid. MS (ES+): m/z: 461.99 (100) [MH⁺]. HPLC: t_r = 1.82 min (ZQ2000: polar_5 min). ¹H ΝMR (400 MHz, DMSO-d₆): 5 = 1.63 - 1.68 (m, 2H), 2.10 (s, 3H), 2.11 (s, 3H), 2.18 - 2.24 (m, 2H), 2.33 - 2.43 (m, 2H), 2.54 - 2.56 (m, 2H), 3.67 - 3.72 (m, 2H), 4.15 (bs, IH), 4.21 (bs, IH), 6.45 (s, IH), 6.84 (d, J= 6.4 Hz, IH), 7.87 (dd, J = 1.6, 8.8 Hz, IH), 8.03 (d, J= 8.8 Hz, IH), 8.34 (s, IH), 8.92 (s, IH), 9.23 (s, IH), 9.61 (s, IH), 12.02 (d, J= 11.2 Hz, IH).

[347] EXAMPLE 110: 6-[l-(3-Hydroxy-2,2-dimethylpropanoyl)-l,2,3,6- tetrahydropyridin-4-yl]-iV-l,3-benzothiazol-6-yI-7H-pyrrolo[2,3-Λf|pyrimidin-4-amine.

[348] To a mixture of benzothiazol-6-yl-[6-(l,2,3,6-tetrahydropyridin-4-yl)-7H- pyrrolo[2,3-^]pyrimidin-4-yl]amine trihydrochloride (50.0mg, 0.1 lmmol) in DMF (3mL) was added 2,2-dimethyl-3-hydroxypropionic acid (150mg, 1.3mmol), TBTU (42.0mg, 0.13mmol) and N,N-diisopropylethylamine (O.lmL, 0.50mmol). The reaction mixture stirred at rt for 16h. The mixture was concentrated in vacuo and purified via MDP, which afforded the title compound as yellow solid. MS (ES+): m/z: 448.96 (100) [MH⁺]. HPLC: t_t = 2.35 min (ZQ2000: polar_5 min). ¹HNMR (400 MHz, DMSO-d₆): δ = 1.20 (s, 6H), 3.19 (s, IH), 3.46 (s, 2H), 3.79 - 3.81 (m, 2H), 4.21 (s, 2H), 4.59 (bs, IH), 6.43 (s, IH), 6.84 (d, J= 1.6 Hz, 1H),7.87 (dd, J= 1.6, 8.8 Hz, IH), 8.03 (d, J= 8.8 Hz, IH), 8.34 (s, IH), 8.91 (d, J= 2.0 Hz, IH), 9.23 (s, IH), 9.62 (s, IH), 12.03 (s, IH). [349] EXAMPLE 111: 6-[l-(2,2-Dimethyl-3-oxopropanoyl)-l,2,3,6-tetra- hydropyridin-4-yI]-iV-l,3-benzothiazol-6-yl-7_Jff-pyrrolo[2,3-d]pyrimidin-4-amine.

[350] To a solution of 6-[l-(3-hydroxy-2,2-dimethylpropanoyl)-l,2,3,6- tetraliydropyridin^-yl]-N-l,3-benzoώiazol-6-yl-7H-pyrrolo[2,3-d]pyrimidin-4-amine (Example 110) (150mg, 0.33mmol) in DMSO (4mL) was added EDC (190mg, lmmol). The reaction mixture stirred at rt for 5h. The mixture was taken up in a large amount of EtOAc and extracted with water. The combined organic extracts were dried over sodium sulfate and concentrated in vacuo, which afforded the title compound as a yellow solid. MS (ES+): m/z: 446.93 (100) [MH⁺]. HPLC: t_r = 2.53 min (ZQ2000: polar_5 min). ¹H ΝMR (400 MHz, DMSO-d₆): δ = 1.37 (s, 6H) 3.39 - 3.69 (m, 3H), 3.70 - 4.22 (m, 3H), 6.21 (bs, IH), 6.82 (s, IH), 6.84 (d, J= 1.6 Hz, IH), 7.87 (dd, J= 1.6, 8.8 Hz, IH), 8.03 (d, J= 8.8 Hz, IH), 8.34 (s, IH), 8.91 (d, J= 2.0 Hz, IH), 9.23 (s, IH), 9.62 (s, IH), 12.03 (s, IH). [351] EXAMPLE 112: 6-{l-[4-(Dimethylamino)butanoyI]-l,2,3,6-tetra- hydropyridin-4-yl}-iV-l,3-benzothiazol-6-yl-7H-pyrrolo[2,3-rflpyrimidin-4-amine.

[352] The procedure for EXAMPLE 109 was followed except for replacing 2,2- dirnethyl-3-hydroxypropionic acid with 2,2-dimethyl-3-piperidin-l-ylpropanoic acid. The mixture was purified via MDP, which afforded the title compound as a yellow solid. MS (ES+): m/z: 516.06 (100) [MH⁺]. HPLC: t_t = 1.98 min (ZQ2000: polar_5 min). ¹H ΝMR (400 MHz, DMSO-d₆): δ = 1.21 (s, 6H), 1.26 - 1.28 (m, 2H), 1.37 - 1.41 (m, 5H), 2.30 - 2.34 (m, 5H), 2.47 - 2.49 (m, 2H), 3.75 - 3.77 (m, 2H), 4.26 (s, 2H), 6.44 (s, IH), 6.82 (d, J= 2.0 Hz, IH), 7.87 (dd, J= 2.4, 8.8 Hz, IH), 8.03 (d, J= 8.8 Hz, IH), 8.34 (s, IH), 8.91 (d, J= 2.0 Hz, IH), 9.23 (s, IH), 9.59 (s, IH), 12.01 (s, IH). [353] 2,2-Dimethyl-3-piperidin-l-ylpropanoic acid.

HO_S d

[354] To a solution of benzyl-2,2-dimethyl-3-piperidin-l-ylpropanoate (117.0mg,

0.42 mmol) in ethanol (5mL) was slowly added 10% wt Palladium in carbon (50mg, 0.05mmol). The reaction mixture was left to stir at rt for Ih under hydrogen. The mixture was filtered through Celite and concentrated in vacuo, which afforded the title compound as a yellow solid. 'H NMR (400 MHZ, CDCl₃): δ = 1.22 (s, 6H), 1.28 - 1.39 (bs, 2H), 1.74 - 1.79 (m, 4H), 2.76 (s, 2H), 2.79 - 3.08 (bs, 4H). [355] Benzyl-2,2-dimethyl-3-piperidin-l-ylpropanoate.

[356] To a solution of benzyl-2,2-dimethyl-3-oxopropanoate (200mg, l.Ommol) in

DCM (3OmL) were added piperidine (0.1OmL, l.lmmol) and sodium triacetoxyborohydride (400mg, 2.0mmol). The reaction mixture was left to stir at rt for 16h. The mixture was partitioned between DCM and water and treated with saturated NaHCO₃. The combined organic extracts were dried over Na₂SO₄ and concentrated in vacuo. Purification via silica gel chromatography (5% EtOAc in Hexane) afforded the title compound as a yellow oil. MS (ES+): m/z: 276.18 (100) [MH⁺]. HPLC: 4 = 1.97 min (ZQ2000: polar_5 min). ¹H NMR (400 MHz, CDCl₃): δ = 1.17 (s, 6H), 1.28 - 1.37 (m, 2H), 1.40 - 1.46 (m, 4H), 2.34 - 2.36 (m, 4H), 2.44 (s, 2H), 5.09 (s, 2H), 7.25 - 7.34 (m, 5H). [357] Benzyl-2,2-dimethyl-3-oxopropanoate.

[358] A mixture of DMSO (1OmL, 200mmol) and DCM (0.2mL) was added to a mixture of oxalyl chloride (8.ImL, 0.096 mol) and DCM (35OmL) at -72°C. The resulting mixture was left to stir for 30min at-72°C. To the mixture was added l-benzyl-3-hydroxy- 2,2-dimethylpropanoate (5g, 19.2mmol) in DCM (30OmL). The reaction mixture stirred at- 72⁰C for 30min. The reaction was quenched with triethylamine (67mL, 0.48 mol) and the reaction was allowed to slowly warm to rt. The mixture was partitioned between DCM and water, treated with saturated sodium bicarbonate and brine, dried over Na₂SO₄ and concentrated in vacuo, which afforded the title compound as a yellow oil. ¹H NMR (400 MHz, CDCl₃): δ = 1.35 (s, 6H), 5.11 (s, 2H), 7.31 - 7.39 (m, 5H), 9.68 (s, IH). [359] l-BenzyI-3-hydroxy-2,2-dimethyIpropanoate.

[360] To a solution of 2,2-dimethyl-3-hydroxypropionic acid (1Og, 86.3mmol) in methanol (55mL) and water (6mL) was added cesium carbonate (1Og, 30.0mmol) as a 20% solution in water. The reaction mixture was left to stir at rt for 15min. The mixture was concentrated in vacuo and the water was removed by making an azeotrope with toluene and concentrating it down. This process was repeated 3x and it yielded a white solid. The resulting solid was dissolved in DMF (55mL) and benzyl bromide (8.2OmL, 68.9mmol) was added. The reaction was left to stir at rt for 16h. The mixture was partitioned between water and EtOAc. The organic layer was further partitioned between ethylacetate and sodium bicarbonate solution to remove excess acid. The organic extracts were dried over sodium sulfate, filtered and concentrated in vacuo, which afforded the product as a yellow oil. ¹H NMR (400 MHz, CDCl₃): δ = 1.21 (s, 6H), 2.77 (bs, IH), 3.57 (s, 2H), 5.13 (s, 2H), 7.26 - 7.43 (m, 5H).

[361] EXAMPLE 113: 6-[l-(2,2-DimethyI-4-methyIpiperazin-l-yIpropanoyl)- l,2,3,6-tetrahydropyridin-4-yI]-7V-l,3-benzothiazol-6-yl-7H-pyrroIo[2,3-rf|pyrimidin-4- amine.

[362] The procedure from EXAMPLE 110 was followed except for replacing 2,2- dimethyl-3-hydroxypropionic acid with 2,2-dimethyl-3-(4-methylpiperazin-l-yl)propanoic acid. The mixture was precipitated with water and the gravity filtration afforded the title compound as a tan solid. MS (ES+): m/z: 531.04 (10) [MH⁺]. HPLC: I_x = 1.94 min (ZQ2000: polar_5 min). ¹H NMR (400 MHz, DMSO-d₆): δ = 1.21 (s, 6H), 2.04 (s, 3H), 2.06 - 2.20 (m, 4H), 2.23 - 2.38 (m, 4H), 2.51 - 2.52 (m, 4H), 3.75 - 3.77 (m, 2H), 4.23 (s, 2H), 6.44 (s, IH), 6.82 (d, J= 2.0 Hz, IH), 7.87 (dd, /= 2.4, 8.8 Hz, IH), 8.03 (d, J= 8.8 Hz, IH), 8.33 (s, IH), 8.91 (d, /= 2.0 Hz, IH), 9.22 (s, IH), 9.58 (s, IH), 12.01 (s, IH). [363] 2,2-DimethyI-3-(4-methyIpiperazin-l-yI)propanoic acid.

[364] The procedure for 2,2-dimethyl-3-piperidin-l -ylpropanoic acid was followed except for replacing benzyl-2,2-dimethyl-3-piperidin-l-ylpropanoate with benzyl 2,2- dimethyl-3-(4-methylpiperazin-l-yl)propanoate. The compound was obtained as a yellow solid. ¹H NMR (400 MHz, CDCl₃): δ = 1.24 (s, 6H), 2.33 (s, 3H), 2.44 - 2.92 (m, 10H). [365] Benzyl 2,2-dimethyl-3-(4-methyIpiperazin-l-yl)propanoate.

[366] The procedure for benzyl-2,2-dimethyl-3-piperidin-l -ylpropanoate was followed except for replacing piperidine with 1-methylpiperazine. Purification via silica gel chromatography (5% EtOAc in hexane) afforded the title compound as a yellow oil. MS (ES+): m/z: 291.20 (100) [MH⁺]. HPLC: t_r = 2.08 min (ZQ2000: polar_5 min). ¹H NMR (400 MHz, CDCl₃): δ = 1.18 (s, 6H), 2.09 (s, 3H), 2.23 - 2.33 (m, 4H), 2.39 - 2.50 (m, 6H), 5.11 (s, 2H) 7.31 - 7.36 (m, 5H).

[367] General procedure for preparation of an a,a-dimethylpropane-l-one library:

[368] To a solution of benzothiazol-6-yl-[6-(l ,2,3,6-tetrahydropyridin-4-yl)-7H- pyrrolo[2,3-d]pyrimidin-4-yl]-amine tris-hydrochloride (525.0mg) in DMF (12mL) and dichloromethane (ImL) at 4°C was added NN-diisopropylethylamine (3eq.) followed by 3- chloropivaloyl chloride (0.178g, l.Oeq). The resulting mixture was allowed to warm up to rt and left overnight before it was applied for next step reaction without any further purification. The mixture was divided into 13 aliquots, and lmg of KI, 5eq. of NN-diisopropylethylamine, and 10eq. of corresponding amine were added. If an amine was used as hydrochloride, additional 2eq. of NN-diisopropylethylamine were added. The solutions were degassed with N₂ and heated at 8O⁰C for 96h. The products were purified by preparative HPLC with water / acetonitrile /formic acid mixture and are assumed to be formate salts. [369] EXAMPLE 114: l-{4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-rfl- pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yI}-3-chloro-2,2-dimethylpropan-l-one.

[370] LC/MS: m/z 466.89/468.92 [MH⁺] (100/35), fe = 2.81 min (ZQ2000, polar_5min).

[371] EXAMPLE 115: l-{4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2J?-pyridin-l-yl}-2,2-dimethyl-3-pyrrolidin-l-ylpropan-l- one.

[372] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSOd₆): δ = 12.01 (s, IH), 9.60 (s, IH), 9.23 (s, IH), 8.91 (d, IH, J= 2.0 Hz), 8.32 (s, IH), 8.21 (s, 2H), 8.05 (d, IH, J= 8.9 Hz), 7.88 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.83 (s, IH), 6.43 (s, IH), 4.24 (br s, 2H), 3.76 (t, 2H, J= 5.7 Hz), 3.41 (m, 6H), 2.67 (s, 2H), 1.60 (m, 4H), 1.23 (br s, 6H). LC/MS: m/z 502.03 [MH⁺] (100), t_κ = 1.92 min (ZQ2000, polar_5min). [373] EXAMPLE 116: l-{4-[4-(Benzothiazol-6-yIamino)-7H-pyrrolo[2,3-d]- pyrimidin-6-yl]-3,6-dihydro-2iϊ-pyridin-l-yl}-3-diethylamino-2,2-dimethylpropan-l- one.

[374] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.94 (d, IH, J= 15.8 Hz), 9.48 (s, 1H), 9.17 (s, IH), 8.85 (d, IH, J= 2.0 Hz), 8.25 (s, IH), 8.13 (s, 2H), 7.96 (d, IH, J= 8.9 Hz), 7.79 (dd, IH, J== 2.0 Hz & 8.9 Hz), 6.76 (br s, IH), 6.37 (br s, IH), 4.21 (br s, 2H), 3.71 (t, 2H, J= 5.3 Hz), 2.52 (br s, 2H), 2.40 (m, 6H), 1.14 (s, 6H), 0.82 (t, 6H, J= 7.0 Hz). LC/MS: m/z 504.06 (95) [MH⁺], t_R = 1.92 min (ZQ2000, polar_5min).

[375] EXAMPLE 117: l-{4-[4-(Benzothiazol-6-yIamino)-7H-pyrroIo[2,3-rf]- pyrimidin-ό-yy-Sjό-dihydro^jH-pyridin-l-ylJ-S-tert-butylamino^^-dimethylpropan-l- one.

[376] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.98 (s, IH), 9.56 (s, IH), 9.19 (s, IH), 8.85 (d, IH, J= 2.0 Hz), 8.24 (s, IH), 8.15 (s, 2H), 7.97 (d, IH, J= 8.9 Hz), 7.79 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.78 (s, IH), 6.37 (br s, IH), 4.14 (s, 2H), 3.75 (t, 2H, J= 5.4 Hz), 2.71 (s, 2H), 2.52 (br s, 2H), 1.26 (s, 6H), 1.09 (s, 9H). LC/MS: m/z 504.06 [MH⁺] (95), t_R = 1.99 min (ZQ2000, polar_5min).

[377] EXAMPLE 118: l-{4-[4-(Benzothiazol-6-yIamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yl}-3-dimethylaniino-2,2-dimethylpropan-l- one.

[378] Following the general procedure, but saturating the reaction mixture with dimethylamine gas in a sealed tube and conducting the reaction at rt for 4 d, the title compound was isolated as yellow powder. LC/MS: m/z 476.06 [MH⁺] (45), fa = 1.85 min (ZQ2000, polar_5min). [379] EXAMPLE 119: l-{4-[4-(BenzothiazoI-6-ylamino)-7H-pyrrolo[2,3-rfl- pyrimidin-6-yl]-3,6-dihydro-2jH-pyridin-l-yI}-3-(3-hydroxypyrrolidin-l-yl)-2,2- dimethylpropan-1-one.

[380] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.95 (s, IH), 9.54 (s, IH), 9.17 (s, IH), 8.85 (d, IH, J= 2.0 Hz), 8.24 (s, IH), 8.16 (s, 2H), 7.97 (d, IH, J= 8.9 Hz), 7.78 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.77 (d, IH), 6.37 (br s, IH), 4.17 (br s, 2H), 4.01 (m, IH), 3.71 (t, 2H, J= 5.2 Hz), 3.15 (m, IH), 2.74 (m, IH), 2.52 (br s, 2H), 2.51 (m, 2H), 2.26 (dd, IH, J= 4.0 Hz & 9.6 Hz), 2.08 (s, IH), 1.77 (m, IH), 1.38 (m, IH), 1.15 (s, 6H). LC/MS: m/z 518.02 [MH⁺] (50), t_κ = 1.87 min (ZQ2000, polar_5min).

[381] EXAMPLE 120: 3-Azepan-l-yl-l-{4-[4-(benzothiazol-6-ylamino)-7H- pyrroloP^-^pyrimidin-ό-yll-Sjό-dihydro^jH-pyridin-l-ylJ^^-dimethylpropan-l-one.

[382] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.96 (s, IH), 9.53 (s, IH), 9.19 (s, IH), 8.85 (d; IH, J= 2.1 Hz), 8.27 (s, IH), 8.09 (s, 2H), 7.97 (d, IH, J= 8.7 Hz), 7.80 (dd, IH, J= 2.1 Hz & 8.7 Hz), 6.77 (s, IH), 6.37 (s, IH), 4.20 (s, 2H), 3.73 (t, 2H, J= 5.3 Hz), 3.29 (t, IH, J-- 6.0 Hz), 3.22 (t, IH, J= 6.0 Hz), 2.74 (s, 2H), 2.68 (t, 4H, J= 8.6 Hz), 1.48 (br s, 4H), 1.41 (br s, 4H), 1.15 (br s, 6H). LC/MS: m/z 530.03 [MH⁺] (15), t_R = 2.03 min (ZQ2000, polar_5min).

[383] EXAMPLE 121: l-{4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yl}-3-(4-hydroxypiperidin-l-yl)-2,2- dimethylpropan-1 -one.

[384] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.97 (s, IH), 9.53 (s, IH), 9.17 (s, IH), 8.84 (d, IH, J= 2.0 Hz), 8.28 (s, IH), 8.10 (s, 2H), 7.98 (d, IH, J= 8.9 Hz), 7.83 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.67 (s, IH), 6.36 (s, IH), 4.19 (br s, 2H), 3.71 (t, 2H, J= 5.5 Hz), 3.50 (m, 2H), 3.29 (m, IH), 2.62 (m, 2H), 2.52 (m, 2H), 2.08 (t, 2H, J= 9.4 Hz), 1.54 (m, 2H), 1.25 (m, 2H), 1.15 (s, 6H). LCMS: m/z 532.05 [MH⁺] (15), t_κ = 1.89 min (ZQ2000, polar_5min). [385] EXAMPLE 122: l-{4-[4-(BenzothiazoI-6-ylamino)-7H-pyrrolo[2,3-rfl- pyrimidra-6-yI]-3,6-dihydro-2iy-pyridin-l-yl}-3-(4-isopropylpiperazin-l-yl)-2,2- dimethylpropan-1-one.

[386] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.95 (s, IH), 9.53 (s, IH), 9.18 (s, IH), 8.85 (s, IH), 8.27 (s, IH), 8.13 (s, 2H), 7.97 (d, IH, J= 9.7 Hz), 7.80 (d, IH, J= 9.7 Hz), 6.76 (s, IH), 6.37 (br s, IH), 4.17 (br s, 2H), 3.68 (t, 2H, J= 5.4 Hz), 3.35 (m, 4H), 2.31 (br s, 8H), 1.15 (s, 6H), 0.75 (d, 6H, J= 6.4 Hz). LC/MS: m/z 559.10 [MH⁺] (20), t_R = 1.98 min (ZQ2000, polar_5min).

[387] EXAMPLE 123: l-{4-[4-(BenzothiazoI-6-yIamino)-7H-pyrroIo[2,3-rf]- pyrimidin-ό-yll-Sjό-dihydro^H-pyridin-l-ylJ^^-dimethyl-S-morpholm^-ylpropan-l- one.

[388] Following the genera procedur>e, trhe title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSOd₆): δ = 11.96 (s, IH), 9.54 (s, IH), 9.17 (s, IH), 8.85 (d, IH₁ J= 2.0 Hz), 8.31 (s, IH), 8.01 (s, 2H), 7.97 (d, IH, J= 8.6 Hz), 7.81 (dd, IH, J= 2.0 Hz & 8.6 Hz), 6.76 (s, IH), 6.38 (br s, IH), 4.18 (br s, 2H), 3.69 (m, 6H), 3.38 (t, 2H, J= 4.4 Hz), 2.52 (m, 2H), 2.32 (t, 2H, J= 4.4 Hz), 2.17 (s, 2H), 1.15 (s, 6H). LC/MS: m/z 518.02 [MH⁺] (100), *_R = 1.91 min (ZQ2000, polar_5min).

[389] EXAMPLE 124: l-{4-[4-(BenzothiazoI-6-ylamino)-7iy-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2£r-pyridin-l-yl}-3-(4,4-difluoropiperidin-l-yl)-2,2- dimethylpropan-1-one.

[390] Following the general procedure, but using 4,4-difluoropiperidine hydrochloride and an additional 2eq. of NN-diisopropylethylamine, the title compound was isolated as yellow powder. ¹H ΝMR (400 MHz, DMSO-d6): 5 = 11.96 (s, IH), 9.54 (s, IH), 9.16 (s, IH), 8.84 (d, IH, J= 2.0 Hz), 8.24 (s, IH), 8.11 (s, 2H), 7.97 (d, IH, J= 8.8 Hz), 7.80 (dd, IH, J= 2.0 Hz & 8.8 Hz), 6.77 (s, IH), 6.38 (br s, IH), 4.18 (br s, 2H), 3.66 (t, 2H, J= 5.7 Hz), 3.10 (m, 4H), 2.52 (m, 2H), 1.77 (m, 2H), 1.07 (s, 6H), 1.04 (m, 4H). LC/MS: rn/z 552.09 [MH⁺] (10), fe= 1.99 min (ZQ2000, polar_5min).

[391] EXAMPLE 125: l-{4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-rfl- pyrimidin-6-yl]-3,6-dihydro-2_JEi^r-pyridin-l-yl}-3-(3,5-dimethylpiperazin-l-yl)-2,2- dimethylpropan-1-one.

[392] Following the general procedure, the title compound was isolated as yellow powder. ¹H ΝMR (400 MHz, DMSOd₆): δ = 11.98 (s, IH), 9.58 (s, IH), 9.17 (s, IH), 8.85 (d, IH, J= 2.0 Hz), 8.27 (s, IH), 8.21 (s, 2H), 7.97 (d, IH, J= 8.9 Hz), 7.77 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.78 (d, IH, J= 4.1 Hz), 6.38 (br s, IH), 4.19 (s, 2H), 3.69 (t, 2H, J= 5.2 Hz), 2.84 (m, 4H), 2.64 (br s, 2H), 2.61 (br s, 2H), 2.52 (br s, 2H), 1.86 (t, 2H, J= 11.0 Hz), 1.16 (s, 6H), 0.89 (d, 6H, J= 6.3 Hz). LC/MS: m/z 545.07 [MH⁺] (15), t_κ = 1.96 min (ZQ2000, polar_5min).

[393] EXAMPLE 126: l-{4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yl}-2-(2-methoxyethoxy)-ethanone.

[394] To a suspension of benzothiazol-6-yl-[6-(l ,2,3,6-tetrahydropyridin-4-yl)-7H- pyrrolo[2,3-rf]pyrimidin-4-yl]-amine tris-hydrochloride (138.0mg, 0.2984mmol), 1- hydroxybenzotriazole (40.8mg, 0,302mmol), and PS-Carbodiimide (1.37mmol/g loading; 873mg, 1.20mmol) in anhydrous N,N-dimethylformamide (1OmL), NN- diisopropylethylamine (260μL, 1.5mmol) was added. A small amount of sonication was used to get majority of solid into solution. 2-(2-Methoxyethoxy)acetic acid (45.7mg, 0.334mmol) in anhydrous DMF (ImL) was added, and the reaction was vigorously shaken at rt for 5.5h. An additional 0.2eq of 2-(2-methoxyethoxy)acetic acid (8.1mg, O.OόOmmol) in anhydrous N^V-dimethylformamide (0.5mL) was added (after 7h), and the reaction was shaken overnight at rt. The resin was filtered off (M-size frit) and rinsed several times with DMF. The filtrate was concentrated in vacuo at medium temp (bath temp: max 43 ⁰C), redissolved in MeOH and DCM, and concentrated again under reduced pressure. The crude material was adsorbed onto Hydrornatrix, dry loaded, and purified by chromatography on silica gel [Jones Flashmaster, 1Og / 7OmL cartridge, eluting with MeOH:DCM 2% → 5% → 10%]. Fractions containing product were combined and concentrated in vacuo, affording the title compound, as an off-white solid. The material was further purified by trituration in MeOH / sonication, affording the title compound, as an off-white solid. ¹H NMR (400 MHz, DMSO-J₆): δ = 2.36-2.56 (s, br, rotamers, 2H), 3.19 (s, 3H), 2.38-2.45 (m, 2H), 3.49-3.55 (m, 2H), 3.58 & 3.64 (t, J= 5.2 Hz, rotamers, 2H), 4.08 & 4.10 (s, br, rotamers, 2H), 4.14 & 4.18 (s, rotamers, 2H), 6.37 (s, br, IH), 6.77 & 6.78 (s, rotamers, IH), 7.80 (dd, J= 8.8, 2.0 Hz, IH), 7.97 (d, J = 8.8 Hz, IH), 8.28 (s, IH), 8.85 (s, IH), 9.17 (s, IH), 9.54 (s, -NH), 11.95 (d, /= 9.2 Hz, - NH). MS (ES+): m/z 465.01 (100) [MH⁺]. HPLC: ,_R = 2.24 min (ZQ2000, polar_5min). [395] EXAMPLE 127: 4-[4-(Benzothiazol-6-ylamino)-7H-pyrroIo[2,3-rfj- pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-ylmorpholin-4-yImethanone.

[396] To a suspension of benzothiazol-6-yl-[6-(l ,2,3,6-tetrahydropyridin-4-yl)-7H- pyrrolo[2,3-J]pyrimidin-4-yl]-amine tris-hydrochloride (200mg, 0.44mmol) in NN- dimethylformamide (4mL) was added N,N-diisopropylethylamine (0.5mL, 3mmol). The reaction mixture was stirred at O⁰C for 5min prior to the addition of 4-chloro- carbonylmorpholine (65mg, 0.44mmol) in DMF (0.5mL). The resulting mixture was stirred at O⁰C for Ih, diluted with EtOAc (3OmL), washed with water (2 x 15mL), brine (15mL), and dried over anhydrous sodium sulfate. The filtrate was concentrated to 5mL, and the resulting off-white solid was collected by filtration to give the title compound. LC-MS (ES, Pos.): 462 [MH⁺], and ¹H ΝMR (DMSO-d₆, 400 MHz): δ = 2.53 (m, 2H), 3.17 (m, 4H), 3.43 (m, 2H), 3.60 (m, 4H), 3.96 (m, 2H), 6.42 (s, IH), 6.82 (d, J = 1.2 Hz, IH), 7.88 (dd, J= 8.8 Hz, 2.0 Hz, IH), 8.04 (d, J= 8.8 Hz, IH), 8.34 (s, IH), 8.91 (d, J= 2.0 Hz, IH), 9.23 (s, IH), 9.60 (s, IH), 12.0 (s, IH).

[397] EXAMPLE 128: {4-[4-(BenzothiazoI-6-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yI]-3,6-dihydro-2H-pyridin-l-yl}-(l-hydroxymethylcyclopropyl)- methanone.

[398] To a suspension of benzothiazol-6-yl-[6-(l,2,3,6-tetrahydropyridin-4-yl)-7H- pyrrolo[2,3-d]pyrimidin-4-yl]-amine tris-hydrochloride (230mg, 0.50mmol) in N₅N- dimethylformamide (4mL) were added NN-diisopropylemylamine (0.7mL, 4.0mmol), 1- hydroxymethyl-cyclopropanecarboxylic acid (70mg, 0.6mmol) and 2-(lH-benzotriazol-l-yl)- 1,1,3,3-tetramethyluronium tetrafluoroborate (190mg, O.όmmol). The resulting mixture was stirred at rt overnight. The mixture was diluted with water (3OmL), and the precipitate was collected by filtration and dried in vacuum, giving the title compound as brown solid. LC-MS (ES, Pos.): 447 [MH⁺]. ¹H ΝMR (DMSO-d₆, 400 MHz): δ = 0.74 (s, 2H), 0.77 (s, 2H), 2.51 (m, 2H), 3.50 (d, J= 5.9 Hz, 2H), 3.85 (m, 2H), 4.20 (m, 2H), 4.90 (br s, IH), 6.44 (s, IH), 6.84 (s, IH), 7.88 (dd, J= 8.9 Hz, 2.1 Hz, IH), 8.04 (d, J= 8.9 Hz, IH), 8.34 (s, IH), 8.92 (d, J= 2.1 Hz, IH), 9.24 (s, IH), 9.62 (s, IH), 12.02 (s, IH). [399] 1-Hydroxymethylcyclopropanecarboxylic acid

[400] [Ref.: Estieu, K., et al. Tetrahedron Letters, 1996, 37(5), 623-624]: Ethyl a- bromocyclobutanecarboxylate (2.07g, lO.Ommol) was added to a solution of potassium hydroxide (2.8Og, 50.0mmol) in water (5OmL), the resulting mixture was refluxed overnight. Evaporation under reduced pressure to remove most of water, the residue was acidified to pH = 1 with 6Ν HCl, the white solid was filtered off. The filtrate was saturated with solid NaCl, extracted with EtOAc (3x20mL), and the organic layers were combined and dried over anhydrous sodium sulfate. Evaporation afforded a light-yellow oil, which was purified by chromatography on silica gel, eluting with Hex: EtOAc = 50:50 → 30:70 → 100% EtOAc to give the title compound as a colorless oil. ¹H NMR (CDCl₃, 400 MHz): δ = 0.98 (dd, J = 7.1 Hz, 4.2Hz, 2H), 1.38 (dd, J = 7.1 Hz, 4.2Hz, 2H), 3.65 (s, 2H).

[401] EXAMPLE 129: {4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yI]-3,6-dihydro-2H-pyridin-l-yl}-(l-piperidin-l-ylmethyIcyclopropyl)- methanone.

[402] To a solution of {4-[4-(benzoiMazol-6-ylamino)-7H-pyrrolo[2,3-^pyrimidin-

6-yl]-3 ,6-dihydro-2H-pyridin~l -yl} -(I -hydroxymethylcyclopropyl)-methanone (23.Omg, 0.05mmol) in N^V-dimethylformamide (ImL) were added NN-diisopropylethylamine (0.05mL, 0.3mmol) and methanesulfonic anhydride (1 lmg, 0.06mmol). The resulting mixture was stirred at rt overnight. LC-MS showed the reaction produced the desired product, but there was still 70% SM, another 1.2eq. of methanesulfonic anhydride was added.

2h later, LC-MS showed the reaction was complete. To the reaction mixture was added piperidine (0.05mL, 0.5mmol), and the resulting mixture was stirred at rt overnight. LC-MS showed the reaction was complete. The mixture was diluted with MeOH (ImL) and purified by mass-directed purification to give the title compounds as an off-white solid. LC-MS (ES,

Pos.): 514 [MH⁺]. ¹H NMR (CD₃OD, 400 MHz): δ = 0.76 (s, 2H), 0.99 (s, 2H), 1.41-1.54 (m,

6H), 2.42-2.69 (m, 8H), 3.99 (m, 2H), 4.23 (m, IH), 4.50 (m, IH), 6.35 (s, IH), 6.73 (s, IH),

7.78 (dd, J= 8.9 Hz, 2.1 Hz, IH), 8.01 (d, J= 8.9 Hz, IH), 8.29 (s, IH), 8.74 (d, J= 2.1 Hz,

IH), 9.12 (s, IH).

[403] General procedure for preparation of an a-cyclopropylpropane-1-one library:

[404] To the DMF solution of methanesulfonic acid l-{4-[4-(benzothiazol-6- ylamino)-7H-pyrrolo[2,3-</]pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carbonyl}- cyclopropylmethyl ester (578.9mg, divided into 13 aliquots for a 13-member library), prepared as described in the previous example, were added 10eq. of NN-diisopropyl- efliylamine and 10eq. of corresponding amine. If the amines were used as salts, additional

DIPEA was used. The solutions were degassed with N₂ and left at rt for 96h. The products were purified by preparative HPLC with water / acetonitrile /formic acid mixture and are assumed to be formate salts.

[405] EXAMPLE 130: {4-[4-(Benzothiazol-6-ylamino)-7H-pyrroIo[2,3-rf]- pyriniidin-6-yl]-3,6-dihydro-2H-pyridin-l-yl}-[l-(4-methyIpiperazin-l-ylmethyl)- cyclopropyl]-methanone.

[406] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.94 (s, IH), 9.54 (s, IH), 9.17 (s, IH), 8.84 (d, IH, J= 2.0 Hz), 8.27 (s, IH), 8.17 (s, 2H), 7.96 (d, IH, J= 8.9 Hz), 7.80 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.77 (s, IH), 6.39 (s, IH), 4.17 (br s, 2H), 3.74 (br s, 2H), 2.54 (br s, 2H), 2.43 (s, 2H), 2.13 (m, 4H), 2.02 (s, 3H), 0.79 (s, 2H), 0.59 (s, 2H). LC/MS: m/z 528.98 (10) [MH⁺], /_R = 1.90 min (ZQ2000, polar_5min).

[407] EXAMPLE 131: {4-[4-(Benzothiazol-6-ylamino)-7iϊ-pyrroIo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2_JH^r-pyridin-l-yl}-(l-pyrroIidin-l-ylmethylcyclopropyl)- methanone.

[408] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.96 (s, IH), 9.54 (s, IH), 9.16 (s, IH), 8.85 (d, IH, J= 2.0 Hz), 8.26 (s, IH), 8.13 (s, 2H), 7.97 (d, IH, J= 8.9 Hz), 7.81 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.77 (s, IH), 6.38 (s, IH), 4.09 (br s, 2H), 3.74 (m, 2H), 2.53 (s, 2H), 2.52 (m, 2H), 2.47 (m, 2H), 1.55 (s, 4H), 1.05 (d, 2H, J= 6.6 Hz), 0.79 (br s, 2H), 0.60 (dd, 2H, J= 1.7 Hz & 6.6 Hz). LC/MS: m/z 499.57 [MH⁺] (80), t_R = 1.88 min (ZQ2000, polar_5min). [409] EXAMPLE 132: {4-[4-(Benzothiazol-6-ylamino)-7H-pyrroIo[2,3-d]- pyrimidin-6-yI]-3,6-dihydro-2iϊ-pyridin-l-yl}-(l-diethylaminomethyIcyclopropyl)- methanone.

[410] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.96 (s, IH), 9.48 (s, IH), 9.17 (s, IH), 8.85

(d, IH, J= 2.0 Hz), 8.28 (s, IH), 8.12 (s, 2H), 7.97 (d, IH, J= 8.9 Hz), 7.80 (dd, IH, J= 2.0

Hz & 8.9 Hz), 6.77 (s, IH), 6.38 (br s, IH), 4.06 (br s, 2H), 3.71 (t, 2H, J= 5.3 Hz), 2.52 (br s, 2H), 2.51 (m, 4H), 1.08 (t, 2H, J= 7.2 Hz), 0.82 (t, 6H, J= 7.1 Hz), 0.78 (d, 2H, J= 8.5

Hz), 0.60 (t, 2H, J= 7.1 Hz). LC/MS: m/z 502.03 [MH⁺] (100), t_R = 1.93 min (ZQ2000, polar_5min).

[411] EXAMPLE 133: {4-[4-(Benzothiazol-6-ylamino)-7fi-pyrrolo[2,3-«f]- pyrimidin-6-yl]-3,6-dihydro-2iϊ-pyridin-l-yl}-(l-piperidin-l-ylmethylcycIopropyl)- methanone.

[412] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSOd₆): δ = 11.96 (s, IH), 9.54 (s, IH), 9.16 (s, IH), 8.85 (s, IH, J= 2.0 Hz), 8.28 (s, IH), 8.10 (s, 2H), 7.97 (d, IH, J= 8.9 Hz), 7.80 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.77 (s, IH), 6.28 (s, IH), 4.08 (m, 2H), 3.71 (m, 2H), 2.52 (m, 2H), 2.48 (m, 2H), 2.42 (br s, 4H), 1.34 (br s, 4H), 1.25 (br s, 2H), 0.80 (br s, 2H), 0.60 (dd, 2H, J= 1.5 Hz & 6.2 Hz). LC/MS: m/z 514.04 [MH⁺] (100), fo = 1.94 min (ZQ2000, polar_5min). [413] EXAMPLE 134: {4-[4-(Benzothiazol-6-yIamino)-7H-pyrroIo[2,3-rf]- pyrimidin-ό-yll-Sjό-dihydro^H-pyridm-l-ylJ-tl-^ert-butylaminomethylJ-cyclopropyl]- methanone.

[414] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.97 (s, IH), 9.56 (s, IH), 9.17 (s, IH), 8.85 (d, IH, J= 2.0 Hz), 8.24 (s, IH), 8.13 (s, 2H), 7.97 (d, IH, J= 8.9 Hz), 7.77 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.78 (s, IH), 6.39 (br s, IH), 4.19 (br s, 2H ), 3.72 (br s, 2H), 2.74 (s, 2H), 2.52 (br s, 2H), 0.96 (s, 9H), 0.81 (t, 2H, J= 6.9 Hz), 0.75 (t, 2H, J= 6.9 Hz). LC/MS: m/z 501.98 [MH⁺] (70), t_R = 1.93 min (ZQ2000, polar_5min).

[415] EXAMPLE 135: {4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yl}-(l-dimethylaminomethylcyclopropyl)- methanone.

[416] Following the general procedure, but using a sealed tube and saturating the reaction mixture with dimethylamine gas, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.94 (s, IH), 9.55 (s, IH), 9.19 (s, IH), 8.84 (d, IH, J= 2.0 Hz), 8.27 (s, IH), 8.15 (s, 2H), 7.96 (d, IH, J= 8.9 Hz), 7.68 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.78 (s, IH), 6.31 (br s, IH), 4.10 (br s, 2H), 3.78 (br s, 2H), 2.52 (br s, 2H), 2.42 (s, 2H), 2.10 (s, 6H), 0.81 (br s, 2H), 0.56 (t, 2H, J= 4.5 Hz). LC/MS: m/z 474.11 [MH⁺] (70), fe = 1.84 min (ZQ2000, polar_5min).

[417] EXAMPLE 136: {4-[4-(BenzothiazoI-6-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2_JH-pyridin-l-yI}-[l-(3-hydroxypyrroIidin-l-yImethyI)- cyclopropyl] -methanone.

[418] Following the general procedure, the title compound was isolated as yellow powder. ¹HNMR (400 MHz, DMSO-d₆): δ = 11.95 (s, IH), 9.55 (s, IH), 9.17 (s, IH), 8.85 (d, IH, J= 2.0 Hz), 8.24 (s, IH), 8.12 (s, 2H), 7.97 (d, IH, J= 8.9 Hz), 7.78 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.77 (d, IH), 6.36 (br s, IH), 4.07 (m, 2H), 3.72 (m, 2H), 2.78 (m, 2H), 2.54 (m, 2H), 2.52 (br s, 2H), 2.22 (dd, IH, J= 4.2 Hz & 9.7 Hz), 1.85 (m, 2H), 1.40 (m, 2H), 1.07 (d, 2H, J= 6.6 Hz), 0.79 (br s, 2H), 0.60 (t, 2H, J= 5.2 Hz). LC/MS: m/z 515.99 [MH⁺] (75), t_κ = 1.84 min (ZQ2000, polar_5min).

[419] EXAMPLE 137: (l-Azepan-l-ylmethylcyclopropyl)-{4-[4-(benzothiazol-

6-ylamino)-7jH-pyrroIo[2,3-rf]pyrimidin-6-yI]-3,6-dihydro-2H-pyridin-l-yl}-methanone.

[420] Following the general procedure, the title compound was isolated as yellow powder. ¹HNMR (400 MHz, DMSO-d₆): δ = 11.96 (s, IH), 9.53 (s, IH), 9.16 (s, IH), 8.85 (d, IH, J= 2.1 Hz), 8.28 (s, IH), 8.11 (s, 2H), 7.97 (d, IH, J= 8.7 Hz), 7.81 (dd, IH, J= 2.1 Hz & 8.7 Hz), 6.77 (s, IH), 6.39 (s, IH), 4.08 (br s, 2H), 3.73 (br s, 4H), 2.62 (m, 4H), 2.52 (br s, 2H), 1.43 (br s, 4H), 1.40 (br s, 4H), 0.80 (br s, 2H), 0.59 (t, 2H, J= 5.6 Hz). LC/MS: m/z 528.13 [MH⁺] (15), t_κ = 1.94 min (ZQ2000, polar_5min).

[421] EXAMPLE 138: {4-[4-(Benzothiazol-6-yIamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2J3-pyridin-l-yl}-[l-(4-hydroxypiperidin-l-ylmethyl)- cyclopropyl]-methanone.

[422] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.95 (s, IH), 9.49 (s, IH), 9.17 (s, IH), 8.84 (d, IH, J= 2.0 Hz), 8.28 (s, IH), 8.12 (s, 2H), 7.98 (d, IH, J= 8.9 Hz), 7.83 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.77 (s, IH), 6.39 (s, IH), 4.09 (br s, 2H), 3.71 (br s, 2H), 3.50 (m, IH), 3.31 (m, 2H), 2.74 (br s, 2H), 2.52 (br s, 2H), 2.40 (s, IH), 1.98 (t, 2H, J= 9.9 Hz), 1.55 (m, 2H), 1.23 (m, 2H), 0.80 (br s, 2H), 0.58 (t, 2H, J= 1.4 Hz). LC/MS: m/z 529.97 [MH⁺] (20), /_R = 1.86 min (ZQ2000, polar_5min).

[423] EXAMPLE 139: {4-[4-(Benzothiazol-6-yIamino)-7H-pyrrolo[2,3-d]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yl}-[l-(4-isopropylpiperazin-l-ylmethyl)- cyclopropyl]-methanone.

[424] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 12.02 (s, IH), 9.61 (s, IH), 9.26 (s, IH), 8.92

(d, IH, J= 2.0 Hz), 8.34 (s, IH), 8.20 (s, 2H), 8.06 (d, IH, J= 8.9 Hz), 7.83 (dd, IH, J= 2.0

Hz & 8.9 Hz), 6.84 (s, IH), 6.46 (br s, IH), 4.14 (br s, 2H), 3.68 (m, 2H), 3.26 (m, 4H), 2.52

(br s, 2H), 2.49 (br s, 2H), 2.45 (br s, 4H), 2.17 (m, IH), 0.91 (d, 6H, J= 6.0 Hz), 0.88 (br s,

2H), 0.65 (t, 2H, J= 4.8 Hz). LC/MS: m/z 557.02 [MH⁺] (20), *_R = 1.93 min (ZQ2000, polar_5min).

[425] EXAMPLE 140: {4-[4-(Benzothiazol-6-yIamino)-7H-pyrroIo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yI}-(l-morpholin-4-ylmethylcyclopropyl)- methanone.

[426] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.96 (s, IH), 9.54 (s, IH), 9.17 (s, IH), 8.85 (d, IH, J= 2.0 Hz), 8.31 (s, IH), 8.09 (s, 2H), 7.97 (d, IH, J= 8.6 Hz), 7.81 (dd, IH, J= 2.0 Hz & 8.6 Hz), 6.73 (s, IH), 6.33 (br s, IH), 4.17 (br s, 2H), 3.72 (m, 2H), 3.42 (br s, 2H), 2.53 (br s, 2H), 2.35 (br s, 2H), 2.26 (br s, 6H), 0.81 (br s , 2H), 0.58 (t, 2H, J= 5.9 Hz). LC/MS: m/z 515.99 [MH⁺] (50), t_R = 1.87 min (ZQ2000, polar_5min).

[427] EXAMPLE 141: {4-[4-(Benzothiazol-6-ylamino)-7H-pyrroIo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2fi-pyridin-l-yI}-[l-(4,4-difluoropiperidin-l-yImethyl)- cyclopropyl] -methanone.

[428] Following the general procedure, but using 4,4-difluoropiperidine hydrochloride and additional 2eq. of NN-diisopropylethylamine, the title compound was isolated as yellow powder. ¹H ΝMR (400 MHz, DMSOd₆): δ = 11.96 (s, IH), 9.54 (s, IH), 9.16 (s, IH), 8.84 (d, IH, J= 2.0 Hz), 8.24 (s, IH), 7.97 (d, IH, J= 8.8 Hz), 7.80 (dd, IH, /= 2.0 Hz & 8.8 Hz), 6.77 (s, IH), 6.38 (br s, IH), 4.18 (br s, 2H), 3.66 (t, 2H, J= 5.7 Hz), 2.54

(br s, 6H), 1.78 (br s, 6H), 0.81 (s, 2H), 0.60 (t, 2H, J= 5.4 Hz). LC/MS: rø/z 550.01 [MH⁺]

(30), t_R = 2.01 min (ZQ2000, polar_5min).

[429] EXAMPLE 142: {4-[4-(Benzothiazol-6-yIamino)-7J3-pyrrolo[2,3-rf]- pyrimidin-6-yI]-3,6-dihydro-2H-pyridin-l-yI}-(l-{[(2-isopropylaminopropyl)- methylamino]-methyl}-cyclopropyl)-methanone.

[430] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSOd₆): δ = 11.97 (s, IH), 9.57 (s, IH), 9.17 (s, IH), 8.85 (d, IH, J= 2.0 Hz), 8.27 (s, IH), 8.21 (s, 2H), 7.97 (d, IH, J= 8.9 Hz), 7.77 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.78 (s, IH), 6.38 (br s, IH), 4.19 (s, 2H), 3.69 (m, 2H), 2.85 (m, 2H), 2.54 (m, 2H), 2.48 (br s, 2H), 1.61 (t, 2H, J= 10.4 Hz), 0.89 (m, 6H), 0.81 (br s, 2H), 0.59 (br s, 2H). LC/MS: m/z 543.05 [MH⁺] (15), t_R = 1.92 min (ZQ2000, polar_5min). [431] General procedure for the preparation of a urea library:

[432] To a solution of benzothiazol-6-yl-[6-(l ,2,3,6-tetrahydropyridin-4-yl)-7H- pyrrolo[2,3-(f|pyrimidin-4-yl]-amine tris-hydrochloride (396mg, in DMF (12mL) and dichloromethane (ImL) at 4°C was added NN-diisopropylethylamine followed by A- nitrophenyl chloroformate (200mg, 1.Oeq.). The resulting mixture was allowed to warm up to rt and left overnight. This solution of 4-[4-(benzothiazol-6-ylamino)-7H-pyriOlo[2,3- rf]pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid 4-nitrophenyl ester was divided into 10 aliquots, and 5eq. of N,N-diisopropylethylamine and 10eq. of the corresponding amine were added. The solutions were degassed with N₂ and heated at 50⁰C for 96h. The products were purified by preparative HPLC with water / acetonitrile /formic acid mixtures and are assumed to be formate salts.

[433] EXAMPLE 143: 4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid 4-nitrophenyl ester.

[434] LC/MS: m/z 513.94 [MH⁺] (100), t_κ = 3.05 min (ZQ2000, polar_5min). [435] EXAMPLE 144: 4-[4-(Benzothiazol-6-ylamino)-7J2-pyrrolo[2,3-rf]- pyrimidin-6-yI]-3,6-dihydro-2jH-pyridine-l-carboxyIic acid (2-dimethylamino-ethyI)- amide.

[436] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₅): δ = 11.99 (s, IH), 9.60 (s, IH), 9.24 (s, IH), 8.91 (d, IH, J= 2.0 Hz), 8.34 (s, IH), 8.24 (s, 2H), 8.04 (d, IH, J= 8.9 Hz), 7.87 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.84 (s, IH), 6.43 (s, IH), 4.02 (s, 2H), 3.55 (m, 2H), 3.43 (m, 2H), 3.29 (m, 2H), 2.33 (m, 2H), 2.19 (s, 6H). LC/MS: m/z 463.05 [MH⁺] (15), t_R = 1.81 min (ZQ2000, polar_5min).

[437] EXAMPLE 145: 4-[4-(BenzothiazoI-6-ylamino)-7J3-pyrroIo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2Jϊ-pyridine-l-carboxylic acid (2-diethylaniinoethyl)-amide.

[438] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.92 (s, IH), 9.53 (s, IH), 9.17 (s, IH), 8.85 (d, IH, /= 2.0 Hz), 8.27 (s, IH), 8.14 (s, 2H), 7.97 (d, IH, J= 8.9 Hz), 7.81 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.76 (s, IH), 6.47 (t, IH, /= 5.3 Hz), 6.37 (br s, IH), 3.95 (s, 2H), 3.48 (m, 2H), 3.40 (m, 4H), 3.10 (m, 2H), 2.51 (q, 4H, J= 7.1 Hz), 0.93 (t, 6H, J= 7.1 Hz). LC/MS: m/z 491.11 [MH⁺] (30), ^ = 1.88 min (ZQ2000, polar_5min).

[439] EXAMPLE 146: 4-[4-(Benzothiazol-6-ylamino)-7iZ-pyrroIo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid (2-isopropylamino-ethyl)- amide.

[440] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSOd₆): δ = 11.92 (s, IH), 9.53 (s, IH), 9.17 (s, IH), 8.85 (d, IH, J= 2.0 Hz), 8.27 (s, IH), 8.14 (s, 2H), 7.97 (d, IH, J= 8.9 Hz), 7.81 (dd, IH₁ J= 2.0 Hz & 8.9 Hz), 7.00 (t, IH, J= 4.7 Hz), 6.78 (s, IH), 6.38 (br s, IH), 4.07 (s, 2H), 3.52 (t, 2H, J= 5.5 Hz), 3.26 (q, 2H, J= 5.5 Hz), 3.16 (m, IH), 2.86 (t, 2H, J= 5.9 Hz), 2.69 (m, 2H),

1.14 (d, 6H, J= 6.4 Hz). LC/MS: m/z 477.08 [MH⁺] (30), t_R = 1.83 min (ZQ2000, polar_5min).

[441] EXAMPLE 147: 4-[4-(Benzothiazol-6-ylamino)-7J3-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2/?-pyridine-l-carboxyIic acid (2-piperazin-l-ylethyl)- amide.

[442] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.91 (s, IH), 9.52 (s, IH)₃ 9.16 (s, IH), 8.84 (d, IH, J= 2.0 Hz), 8.26 (s, IH), 8.14 (s, 2H), 7.97 (d, IH, J= 8.9 Hz), 7.91 (s, IH), 7.80 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.76 (s, IH), 6.42 (t, IH, J= 5.3 Hz), 6.37 (br s, IH), 3.94 (s, 2H), 3.48 (t, 2H, J= 5.6 Hz), 3.28 (m, 4H), 3.11 (m, 2H), 2.91 (m, 2H), 2.51 (m, 2H), 2.33 (m, 2H), 2.27 (t, 2H, J = 5.3 Hz). LC/MS: m/z 504.06 [MH⁺] (10), t_κ = 1.70 min (ZQ2000, polar_5min).

[443] EXAMPLE 148: 4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2iϊ-pyridine-l-carboxyIic acid (2-diisopropylamino-ethyl)- amide.

[444] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.91 (s, IH), 9.52 (s, IH), 9.16 (s, IH), 8.84 (d, IH, J= 2.0 Hz), 8.26 (s, IH), 8.14 (s, 2H), 7.97 (d, IH, J= 8.9 Hz), 7.91 (s, IH), 7.80 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.77 (s, IH), 6.71 (br s, IH), 6.37 (br s, IH), 3.96 (s, 2H), 3.50 (t, 2H, J= 5.4 Hz), 3.08 (m, 4H), 2.59 (t, TA, J= 12 Hz), 2.45 (br s, 2H), 0.99 (d, 12H, /= 6.6 Hz). LC/MS: m/z 519.10 [MH⁺] (30), h = 1.94 min (ZQ2000, polar_5min). [445] EXAMPLE 149: 4-[4-(BenzothiazoI-6-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2fi-pyridine-l-carboxylic acid (2-methoxyethyl)-amide.

[446] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 12.10 (s, IH), 9.71 (s, IH), 9.35 (s, IH), 9.03 (d, IH, J= 2.0 Hz), 8.46 (s, IH), 8.42 (s, IH), 8.15 (d, IH, J= 8.9 Hz), 8.00 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.95 (s, IH), 6.70 (t, IH, J= 5.6 Hz), 6.55 (br s, IH), 4.14 (s, 2H), 3.68 (t, 2H, J= 5.6 Hz), 3.47 (m, 2H), 3.37 (s, 3H), 3.34 (q, 2H, J= 6.9 Hz), 2.61 (br s, 2H). LC/MS: m/z 450.04 [MH⁺] (100), *_R = 2.20 min (ZQ2000, polar_5min).

[447] EXAMPLE 150: 4-[4-(Benzothiazol-6-yIamino)-7fi-pyrrolo[2,3-d]- pyrimidin-6-yl]-3,6-dihydro-2fi-pyridine-l-carboxylic acid 6is-(2-methoxyethyl)-amide.

[448] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.92 (s, IH), 9.52 (s, IH), 9.16 (s, IH), 8.84 (d, IH, J= 2.0 Hz), 8.26 (s, IH), 8.14 (s, 2H), 7.97 (d, IH, J= 8.9 Hz), 7.91 (s, IH), 7.80 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.75 (s, IH), 6.36'(br s, IH), 3.81 (br s, 2H), 3.38 (t, 4H, J= 6.1 Hz), 3.29 (m, 4H), 3.18 (s, 6H), 2.71 (s, 2H), 2.52 (br s, 2H). LC/MS: m/z 508.04 [MH⁺] (100), t_κ = 2.39 min (ZQ2000, polar_5min).

[449] EXAMPLE 151: 4-[4-(Benzothiazol-6-ylamino)-7H-pyrroIo[2,3-rf]- pyrimidin-6-yI]-3,6-dihydro-2H-pyridine-l-carboxylic acid (2-piperidin-l-ylethyI)- amide.

[450] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 12.02 (s, IH), 9.53 (s, IH), 9.15 (s, IH), 8.84 (d, IH, J= 2.0 Hz), 8.26 (s, IH), 8.14 (s, 2H), 7.97 (d, IH, J= 8.9 Hz), 7.91 (s, IH), 7.80 (dd, IH, /= 2.0 Hz & 8.9 Hz), 6.76 (s, IH), 6.54 (t, IH, J= 5.2 Hz), 6.38 (br s, IH), 3.95 (s, 2H), 3.49 (t, 2H, J= 5.4 Hz), 3.17 (q, 2H, J= 6.4 Hz), 2.55 (m, 6H), 2.51 (br s, 2H), 1.48 (m, 4H), 1.34 (m, 2H). LC/MS: m/z 503.10 [MH⁺] (25), t_R = 1.85 min (ZQ2000, polar_5min). [451] EXAMPLE 152: 4-[4-(Benzothiazol-6-ylammo)-7H-pyrroIo[2,3-rf]- pyrimidin-6-yI]-3,6-dihydro-2H-pyridine-l-carboxyIic acid (2-morpholin-4-yIethyl)- atnide.

[452] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSOd₆): δ = 11.91 (s, IH), 9.52 (s, IH), 9.16 (s, IH), 8.84 (d, IH, J= 2.0 Hz), 8.26 (s, IH), 8.14 (s, 2H), 7.97 (d, IH, J= 8.9 Hz), 7.91 (s, IH), 7.80 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.76 (s, IH), 6.42 (t, IH, J= 5.5 Hz), 6.37 (br s, IH), 3.95 (s, 2H), 3.48 (t, 2H, J= 5.6 Hz), 3.49 (t, 6H, J= 4.4 Hz), 3.11 (q, 2H, J= 6.3 Hz), 2.49 (br s, 2H), 2.31 (m, 4H). LC/MS: m/z 505.07 [MH⁺] (30), & = 1.80 min (ZQ2000, polar_5min). [453] EXAMPLE 153: 4-[4-(Benzothiazol-6-yIamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2J9-pyridine-l-carboxylic acid (2-pyrrolidin-l-ylethyl)- atnide.

[454] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSOd₆): δ = 11.91 (s, IH), 9.52 (s, IH), 9.16 (s, IH), 8.84 (d, IH₅ J= 2.0 Hz), 8.26 (s, IH), 8.14 (s, 2H), 7.97 (d, IH, J= 8.9 Hz), 7.91 (s, IH), 7.80 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.76 (s, IH), 6.41 (t, IH, J= 5.4 Hz), 6.37 (br s, IH), 3.94 (s, 2H), 3.50 (t, 2H, J= 5.5 Hz), 3.18 (q, 2H, J= 6.3 Hz), 2.67 (m, 6H), 2.48 (br s, 2H), 1.68 (t, 4H, J = 3.2 Hz). LC/MS: m/z 489.03 [MH⁺] (55), h = 1-83 min (ZQ2000, polar_5min). [455] The following examples were prepared following the same procedure:

[456] EXAMPLE 154: {4-[4-(BenzothiazoI-6-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2J3-pyridin-l-yl}-piperazin-l-ylmethanone.

[457] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSOd₆): 5 = 11.95 (s, IH), 9.55 (s, IH), 9.17 (s, IH), 8.84 (d, IH, J= 2.0 Hz), 8.27 (s, IH), 8.20 (s, 2H), 7.97 (d, IH, J= 8.9 Hz), 7.80 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.76 (s, IH), 6.35 (s, IH), 4.40 (br s, 4H), 3.89 (s, 2H), 3.36 (t, 2H, J= 5.6 Hz), 3.17 (s, 3H), 2.85 (br s, 2H), 2.52 (br s, 2H). LC/MS: m/z 461.05 [MH⁺] (40), t_κ = 1.77 min (ZQ2000, polar_5min). [458] EXAMPLE 155: {4-[4-(Benzothiazol-6-yIamino)-7H-pyrrolo[2,3-d]- pyrimidin-6-yI]-3,6-dihydro-2ff-pyridin-l-yI}-(4-ethyIpiperazin-l-yl)-methanone.

[459] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSOd₆): δ = 11.92 (s, IH), 9.53 (s, IH), 9.16 (s, IH), 8.84 (d, IH, J= 2.0 Hz), 8.27 (s, IH), 8.10 (s, 2H), 7.97 (d, IH, J= 8.9 Hz), 7.80 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.76 (s, IH), 6.34 (s, IH), 3.86 (br s, 2H), 3.34 (t, 2H, J= 5.6 Hz), 3.11 (br s, 4H), 2.54 (br s, 2H), 2.30 (d, 4H, J= 6.6 Hz), 2.29 (q, 2H, J= 7.1 Hz), 0.94 (t, 3H, J= 7.1 Hz). LC/MS: m/z 489.08 [MH⁺] (30), t_κ = 1.81 min (ZQ2000, polar_5mrn). [460] EXAMPLE 156: {4-[4-(BenzothiazoI-6-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yl}-(4-isopropylpiperazin-l-yl)-methanone.

[461] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSOd₆): δ = 11.92 (s, IH), 9.54 (s, IH), 9.17 (s, IH), 8.84 (d, IH, J= 2.0 Hz), 8.27 (s, IH), 8.10 (s, 2H), 7.96 (d, IH, J= 8.9 Hz), 7.80 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.71 (s, IH), 6.39 (s, IH), 3.87 (br s, 4H), 3.34 (t, 4H, J= 5.3 Hz), 3.11 (br s, 4H), 2.63 (m, IH), 2.54 (br s, 2H), 0.92 (d, 6H, J= 6.5 Hz). LC/MS: m/z 503.05 [MH⁺] (50), ήs_. = 1.85 min (ZQ2000, polar_5min).

[462] EXAMPLE 157: {4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2_JH-pyridin-l-yl}-(3,5-dimethylpiperazin-l-yl)-methanone.

[463] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSOd₆): δ = 11.93 (s, IH), 9.53 (s, IH), 9.17 (s, IH), 8.84 (d, IH, J= 2.0 Hz), 8.27 (s, IH), 8.15 (s, 2H), 7.99 (d, IH, J= 8.9 Hz), 7.80 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.76 (s, IH), 6.34 (s, IH), 3.87 (br s, 2H), 3.65 (br s, IH), 3.45 (s, 2H), 3.42 (s, IH), 3.34 (t, IH, J= 5.6 Hz), 2.80 (m, 2H), 2.54 (br s, 2H), 2.38 (m, 2H), 0.96 (d, 6H, J= 6.1 Hz). LC/MS: m/z 489.08 [MH⁺] (30), t_R = 1.82 min (ZQ2000, polar_5min).

- I ll - [464] EXAMPLE 158: {4-[4-(BenzothiazoI-6-ylamino)-7H-pyrroIo[2,3-rf]- pyrimidm-6-yl]-3,6-dihydro-2H-pyridin-l-yI}-(4-cyclopentylpiperazin-l-yI)-methanone.

[465] Following the general procedure, the title compound was isolated as yellow powder. ¹HNMR (400 MHz, DMSO-d₆): δ = 11.92 (s, IH), 9.53 (s, IH), 9.16 (s, IH), 8.84 (d, IH, J= 2.0 Hz), 8.27 (s, IH), 8.10 (s, 2H), 7.96 (d, IH, J= 8.9 Hz), 7.80 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.75 (s, IH), 6.35 (s, IH), 3.86 (br s, 2H), 3.33 (t, 2H, J= 5.6 Hz), 3.10 (br s, 4H), 2.53 (br s, 2H), 2.43 (m, IH), 2.36 (br s, 4H), 1.69 (m, 2H), 1.53 (m, 2H), 1.43 (m, 2H), 1.26 (m, 2H). LC/MS: m/z 529.08 [MH⁺] (40), t_κ = 1.90 min (ZQ2000, polar_5min). [466] EXAMPLE 159: {4-[4-(BenzothiazoI-6-ylamino)-7JΪ-pyrrolo[2,3-d]- pyrimidin-6-yl]-3,6-dihydro-2iϊ-pyridin-l-yl}-(l-methylazepan-4-yl)-methanone.

[467] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.94 (s, IH), 9.54 (s, IH), 9.17 (s, IH), 8.84 (d, IH, J= 2.0 Hz), 8.27 (s, IH), 8.17 (s, 2H), 7.96 (d, IH, J= 8.9 Hz), 7.80 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.77 (s, IH), 6.39 (s, IH), 3.64 (br s, 2H), 3.36 (t, 6H, J= 6.5 Hz), 2.66 (br s, 2H), 2.56 (m, 2H), 2.52 (br s, 2H), 2.28 (s, 3H), 1.79 (m, 2H). LC/MS: m/z 489.08 [MH⁺] (20), /_R = 1.81 min (ZQ2000, polar_5min).

[468] EXAMPLE 160: {4-[4-(BenzothiazoI-6-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yI]-3,6-dihydro-2H-pyridin-l-yI}-[4-(2-methoxyethyl)-piperazin-l-yl]- methanone.

[469] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSOd₆): δ = 11.92 (s, IH), 9.53 (s, IH), 9.17 (s, IH), 8.84 (s, IH, J= 2.0 Hz), 8.27 (s, IH), 8.10 (s, 2H), 7.97 (d, IH, J= 8.9 Hz), 7.80 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.76 (s, IH), 6.35 (s, IH), 3.86 (br s, 2H), 3.37 (t, 2H, J= 5.8 Hz), 3.34 (t, 2H, J= 5.6 Hz), 3.17 (s, 3H), 3.10 (br s, 4H), 2.53 (br s, 2H), 2.41 (m, 2H), 2.37 (br s, 4H).

LC/MS: m/z 519.10 [MH⁺] (25), fe = 1.82 min (ZQ2000, polar_5mm).

[470] EXAMPLE 161: {4-[4-(BenzothiazoI-6-yIamino)-7H-pyrroIo[2,3-rf]- pyrimidin-6-yI]-3,6-dihydro-2H-pyridin-l-yI}-[4-(2-dimethyIaminoethyl)-piperazin-l- yl]-methanone.

[471] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-ds): δ = 11.93 (s, IH), 9.55 (s, IH), 9.17 (s, IH), 8.84 (d, IH, J= 2.0 Hz), 8.27 (s, IH), 8.16 (s, 2H), 7.96 (d, IH, J= 8.9 Hz), 7.80 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.77 (s, IH), 6.39 (s, IH), 3.87 (br s, 2H), 3.34 (t, 2H, J= 5.1 Hz), 3.11 (br s, 4H), 2.65 (t, 2H, J= 6.3 Hz), 2.53 (br s, 2H), 2.43 (m, 2H), 2.37 (m, 4H), 2.35 (s, 6H). LC/MS: m/z 532.06 [MH⁺] (35), t_κ = 1.82 min (ZQ2000, polar_5min). [472] EXAMPLE 162: 4-[4-(Benzothiazol-6-ylamino)-7#-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid methyl-(l-methyl-piperidin- 4-yI)-amide.

[473] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.92 (s, IH), 9.54 (s, IH), 9.17 (s, IH), 8.84 (d, IH, J= 2.0 Hz), 8.27 (s, IH), 8.14 (s, 2H), 7.96 (d, IH, J= 8.9 Hz), 7.80 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.77 (s, IH), 6.39 (s, IH), 3.80 (br s, 2H), 3.42 (m, 3H), 3.30 (t, 2H, J= 5.3 Hz), 2.80 (d, 2H, J= 10.8 Hz), 2.63 (s, 3H), 2.52 (br s, 2H), 2.13 (s, 3H), 1.94 (t, 2H, J= 11.8 Hz), 1.67 (m, 2H), 1.50 (d, 2H, J= 10.8 Hz). LC/MS: m/z 503.11 [MH⁺] (10), /_R = 1.83 min (ZQ2000, polar_5min).

[474] EXAMPLE 163: {4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2iϊ-pyridin-l-yl}-thiomorpholin-4-ylmethanone.

[475] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.93 (s, IH), 9.53 (s, IH), 9.17 (s, IH), 8.84 (d, IH, J= 2.0 Hz), 8.27 (s, IH), 8.14 (s, 2H), 7.96 (d, IH, J= 8.9 Hz), 7.80 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.75 (s, IH), 6.35 (s, IH), 3.86 (br s, 2H), 3.35 (m, 4H), 2.56 (m, 4H), 2.52 (br s, 2H), 2.43 (m, 2H). LC/MS: m/z 478.02 [MH⁺] (100), t_κ = 2.58 min (ZQ2000, polar_5min). [476] EXAMPLE 164: {4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-<f|- pyrimidm-6-yI]-3,6-dihydro-2H-pyridin-l-yl}-(cis-2,6-dimethylmorpholin-4-yl)- methanone.

[477] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSOd₆): δ = 10.00 (s, IH), 9.61 (s, IH), 9.23 (s, IH), 8.90 (d, IH, J= 2.0 Hz), 8.34 (s, IH), 8.19 (s, 2H), 8.11 (d, IH, J= 8.9 Hz), 7.82 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.79 (s, IH), 6.41 (s, IH), 3.95 (br s, 2H), 3.45 (m, 4H), 2.54 (s, 2H), 2.49 (m, 2H), 2.08 (s, 2H), 1.08 (d, 6H, J= 6.1 Hz). LC/MS: m/z 490.07 [MH⁺] (100), *_R = 2.52 min (ZQ2000, polar_5min).

[478] EXAMPLE 165: {4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yI]-3,6-dihydro-2_JET-pyridin-l-yl}-(4-hydroxypiperidin-l-yl)-methanone.

[479] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.91 (s, IH), 9.53 (s, IH), 9.16 (s, IH), 8.84 (d, IH, J= 2.0 Hz), 8.27 (s, IH), 8.13 (s, IH), 7.97 (d, IH, J= 8.9 Hz), 7.81 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.75 (d, IH, J= 1.8 Hz), 6.35 (s, IH), 4.53 (br s, IH), 3.85 (br s, 2H), 3.56 (m, 2H), 3.31 (m, 2H), 2.81 (m, 2H), 2.53 (br s, 2H), 1.67 (m, 2H), 1.28 (m, 2H). LC/MS: m/z 476.07 [MH⁺] (100), t_κ = 2.16 min (ZQ2000, polar_5min).

[480] EXAMPLE 166: {4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-^l- pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yI}-(3-hydroxypyrroIidin-l-yI)-methanone.

[481] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.93 (s, IH), 9.53 (s, IH), 9.16 (s, IH), 8.85 (d, IH, J= 2.0 Hz), 8.27 (s, IH), 8.10 (s, 2H), 7.96 (d, IH, J= 8.9 Hz), 7.80 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.76 (s, IH), 6.36 (s, IH), 4.17 (br s, IH), 3.86 (br s, 2H), 3.46 (m, IH), 3.42 (m, 2H), 3.22 (m, 2H), 3.04 (d, 2H, J= 10.9 Hz), 1.75 (m, 2H), 1.68 (m, 2H). LC/MS: m/z 462.04 [MH⁺] (100), fe = 2.15 min (ZQ2000, polar_5min).

[482] EXAMPLE 167: 4-[4-(Benzothiazol-6-ylamino)-7if-pyrrolo[2,3-tf]- pyrimidin-6-yl] -3 ,6-dihydro-2fl-py ridine-1-carboxylic acid diethylamide.

[483] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSOd₆): δ = 11.92 (s, IH), 9.53 (s, IH), 9.16 (s, IH), 8.84 (d, IH, J= 2.0 Hz), 8.34 (s, IH), 8.27 (s, 2H), 7.97 (d, IH, J= 8.9 Hz), 7.80 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.76 (s, IH), 6.36 (s, IH), 3.80 (br s, 2H), 3.31 (m, 2H), 3.08 (q, 4H, J= 7.0 Hz), 2.47 (br s, 2H), 1.00 (t, 6H, J= 7.0 Hz). LC/MS: m/z 448.08 [MH⁺] (100), t_R = 2.65 min (ZQ2000, polar_5min).

[484] EXAMPLE 168: Azetidin-l-yI-{4-[4-(benzothiazol-6-ylamino)-7_JH- pyrrolo[2,3-d]pyrimidin-6-yl]-3,6-dihydro-2£r-pyridin-l-yl}-methanone.

[485] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.93 (s, IH), 9.53 (s, IH), 9.16 (s, IH), 8.84 (d, IH, J= 2.0 Hz), 8.26 (s, IH), 8.22 (s, 2H), 7.98 (d, IH, J= 8.9 Hz), 7.80 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.76 (s, IH), 6.34 (s, IH), 3.87 (m, 4H), 3.40 (t, 2H, J= 5.6 Hz), 3.27 (br s, 2H), 2.54 (br s, 2H), 2.10 (m, 2H). LC/MS: m/z 432.03 [MH⁺] (100), t_κ = 2.36 min (ZQ2000, polar_5min).

[486] EXAMPLE 169: {4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-d]- pyriraidin-6-yl]-3,6-dihydro-2H-pyridin-l-yl}-pyrrolidin-l-ylmethanone.

[487] Following the general procedure, the title compound was isolated as yellow powder. ¹HNMR (400 MHz, DMSOd₆): δ = 11.92 (s, IH), 9.52 (s, IH), 9.16 (s, IH), 8.84 (d, IH, J= 2.0 Hz), 8.27 (s, IH), 8.05 (s, 2H), 7.97 (d, IH, J= 8.9 Hz), 7.81 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.75 (s, IH), 6.36 (s, IH), 3.86 (br s, 2H), 3.36 (t, 2H, J= 5.6 Hz), 3.24 (t, 4H, J= 6.3 Hz), 2.52 (br s, 2H), 1.70 (m, 4H). LC/MS: m/z 446.06 [MH⁺] (100), t_κ = 2.52 min (ZQ2000, polar_5min).

[488] EXAMPLE 170: {4-[4-(Benzothiazol-6-yIamino)-7iy-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yI}-(4,4-difluoropiperidin-l-yI)-methanone.

[489] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSOd₆): δ = 11.94 (s, IH), 9.53 (s, IH), 9.17 (s, IH), 8.83 (d, IH, J= 2.0 Hz), 8.26 (s, IH), 8.13 (s, IH), 7.99 (d, IH, J= 8.9 Hz), 7.81 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.76 (d, IH, J= 1.8 Hz), 6.35 (s, IH), 3.91 (br s, 2H), 3.37 (q, 2H, J= 5.8 Hz), 3.22 (t, 4H, J= 4.8 Hz), 2.52 (br s, 2H), 1.93 (m, 4H). LC/MS: m/z 496.02 [MH⁺] (100), t_R = 2.72 min (ZQ2000, polar_5min).

[490] EXAMPLE 171: {4-[4-(BenzothiazoI-6-ylamino)-7i7-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yl}-(4-propylpiperazin-l-yI)-methanone.

[491] Following the general procedure, the title compound was isolated as yellow flakes. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.92 (s, IH), 9.53 (s, IH), 9.16 (s, IH), 8.84 (d, IH, J= 2.0 Hz), 8.27 (s, IH), 8.10 (s, 2H), 7.97 (d, IH, J= 8.9 Hz), 7.80 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.76 (s, IH), 6.34 (s, IH), 3.86 (br s, 2H), 3.34 (m, 2H), 3.29 (m, 2H), 3.10 (br s, 4H), 2.54 (br s, 2H), 2.30 (br s, 2H), 2.18 (t, 2H, J= 7.2 Hz), 1.35 (m, 2H), 0.79 (t, 3H, J= 7.4 Hz). LC/MS: m/z 503.11 (65) [MH⁺], t_κ = 1.89 (ZQ2000, polar_5min). [492] EXAMPLE 172: {4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2_JH^r-pyridin-l-yl}-(4-isobutylpiperazin-l-yI)-methanone.

[493] Following the general procedure, the title compound was isolated as yellow flakes. ¹HNMR (400 MHz, DMSO-d₆): δ = 12.02 (s, IH), 9.76 (s, IH), 9.35 (s, IH), 9.07 (d, IH, J= 2.0 Hz), 8.58 (s, IH), 8.35 (s, IH)₅ 8.20 (d, IH, J= 8.9 Hz), 8.04 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.91 (s, IH), 6.57 (s, IH), 4.10 (br s, 2H), 3.34 (m, 2H), 3.29 (m, 2H), 3.10 (br s, 4H), 2.54 (br s, 2H), 2.30 (br s, 2H), 2.21 (d, 2H, J= 7.4 Hz), 1.90 (m, IH), 1.02 (d, 6H, J= 6.5 Hz). LC/MS: m/z 517.14 (30) [MH⁺], *_R = 1.90 (ZQ2000, polar_5min). [494] EXAMPLE 173: {4-[4-(Benzothiazol-6-ylamino)-7H-pyrroIo[2,3-d]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yl}-[4-(l-ethyIpropyl)-piperazin-l-yl]- methanone.

[495] Following the general procedure, the title compound was isolated as yellow flakes. ¹HNMR (400 MHz, DMSO-d₅): δ - 11.92 (s, IH), 9.53 (s, IH), 9.16 (s, IH), 8.84 (d, IH, J= 2.0 Hz), 8.27 (s, IH), 8.10 (s, IH), 7.97 (d, IH, J= 8.9 Hz), 7.80 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.76 (s, IH), 6.34 (s, IH), 3.86 (br s, 2H), 3.34 (m, 2H), 3.29 (m, 2H), 3.10 (br s, 4H), 2.54 (br s, 2H), 2.30 (br s, 2H), 2.36 (t, IH, J= 6.7 Hz), 1.68 (m, 2H), 1.48 (m, 2H), 1.08 (t, 6H, /= 7.3 Hz). LC/MS: m/z 531.15 (35) [MH⁺], t_κ = 1.95 (ZQ2000, polar_5min). [496] EXAMPLE 174: {4-[4-(BenzothiazoI-6-ylamino)-7H-pyrroIo[2,3-rf]- pyrimidin-6-yI]-3,6-dihydro-2_JET-pyridin-l-yI}-(4-cyclobutylmethyIpiperazin-l-yl)- methanone.

[497] The reaction mixture derived from the preparation of {4-[4-(benzothiazol-6- ylamino)-7H-pyrrolo[2,3-d]pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yl}-piperazin-l- ylmethanone (EXAMPLE 154) was reacted with (bromomethyl)cyclobutane (90mg, 5eq.) in the presence of DIPEA at 60⁰C for 72h before the mixture was purified by HPLC, giving the title compound as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.78 (s, IH), 9.52 (s, IH), 9.16 (s, IH), 8.84 (d, IH, J= 2.0 Hz), 8.26 (s, IH), 8.14 (s, IH), 7.97 (d, IH, J= 8.9 Hz), 7.91 (s, IH), 7.80 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.82 (d, IH, /= 1.7 Hz), 6.57 (br s, IH), 3.94 (s, 2H), 3.46 (m, 4H), 3.36 (m, 4H), 3.18 (m, 4H), 2.54 (br s, 2H), 2.46 (m, IH), 2.34 (m, 3H), 2.03 (m, IH), 1.84 (m, IH), 1.65 (m, IH). LC/MS: m/z 529.17 (15) [MH⁺], t_κ = 1.94 (ZQ2000, polar_5min). [498] General procedure for the preparation of an aminoethylurea library via bromide displacement:

[499] To a solution of benzothiazol-6-yl-[6-(l ,2,3,6-tetrahydropyridiri-4-yl)-7H- ρyrrolo[2,3-^pyrimidin-4-yl]-amine tris-hydrochloride (303mg) in DMF (8mL) at 4°C was added NN-diisopropylethylamine followed by 2-bromoetiiyl isocyanate (lOOmg). The resulting mixture was allowed to warming up to rt and left overnight. To this solution, divided into 8 aliquots, were added 10eq. of NN-diisopropylethylamine and 10eq. of corresponding amine. If an amine was used as hydrochloride, additional 2eq. of NN- diisopropylethylamine were added. The above solutions were degassed with N₂ and heated at 40⁰C for 72h. The products were purified by preparative HPLC with water / acetonitrile /formic acid mixtures and are assumed to be formate salts.

[500] EXAMPLE 175: 4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl] -3,6-dihydro-2H-pyridine-l-carboxylic acid (2-bromoethyl)-amide.

[501] LC/MS: m/z 418.01 (40) [MH⁺-Br], t_R = 1.83 min (ZQ2000, polar_5min).

[502] EXAMPLE 176: 4-[4-(BenzothiazoI-6-ylamino)-7H-pyrrolo[2,3-rfl- pyrimidin-6-yl] -Sjβ-dihydro^H-pyridine-l-carboxylic acid [2-(4-methylpiperazin-l-yl)- ethyl] -amide.

[503] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSOd₆): δ = 11.92 (s, IH), 9.53 (s, IH), 9.17 (s, IH), 8.85 (d, IH, J= 2.0 Hz), 8.28 (s, IH), 8.11 (s, 2H), 7.97 (d, IH, J= 8.9 Hz), 7.81 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.77 (s, IH), 6.44 (t, IH, J= 5.3 Hz), 6.38 (s, IH), 3.95 (br s, 4H), 3.45 (t, 4H, J= 5.6 Hz), 3.11 (q, 4H, J= 6.3 Hz), 2.43 (br s, 2H), 2.35 (t, 4H, J=7.1 Hz), 2.21 (s, 3H). LC/MS: m/z 518.09 [MH⁺] (40), /_R = 1.80 min (ZQ2000, polar_5min). [504] EXAMPLE 177: 4-[4-(BenzothiazoI-6-yIamino)-7iJ-pyrroIo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2jH-pyridine-l-carboxyIic acid (2-fertf-butylaminoethyl)- amide.

[505] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSOd₆): δ = 12.00 (s, IH), 9.63 (s, IH), 9.23 (s, IH), 8.91 (d, IH, J= 2.0 Hz), 8.34 (s, IH), 8.33 (s, 2H), 8.04 (d, IH, J= 8.9 Hz), 7.88 (dd, IH, J= 2.0 Hz & 8.9 Hz), 7.21 (br s, IH), 6.85 (s, IH), 6.45 (s, IH), 4.06 (br s, 2H), 3.60 (m, 2H), 3.35 (q, 4H, J= 5.3 Hz), 2.90 (t, 2H, J= 6.1 Hz), 1.23 (s, 9H). LC/MS: m/z 491.11 [MH⁺] (40), t_R = 1.91 min (ZQ2000, polar_5min).

[506] EXAMPLE 178: 4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-tf]- pyrimidin-6-yI]-3,6-dihydro-2H-pyridine-l-carboxylic acid [2-(3-hydroxypyrrolidin-l- yl)-ethyl] -amide.

[507] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.98 (s, IH), 9.60 (s, IH), 9.23 (s, IH), 8.91 (d, IH, J= 2.0 Hz), 8.34 (s, IH), 8.22 (s, 2H), 8.04 (d, IH, J= 8.9 Hz), 7.88 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.83 (s, IH), 6.57 (t, IH, J= 5.3 Hz), 6.44 (s, IH), 4.19 (m, IH), 4.02 (br s, 2H), 3.56 (m, IH), 3.19 (m, 2H), 2.80 (m, IH), 2.70 (m, IH), 2.56 (br s, 2H), 1.98 (m, IH), 1.56 (m, IH). LC/MS: m/z 505.07 [MH⁺] (15), ,_R = 1.79 min (ZQ2000, polar_5min). [508] EXAMPLE 179: 4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid (2-azepan-l-ylethyl)-amide.

[509] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.92 (s, IH), 9.53 (s, IH), 9.17 (s, IH), 8.85 (d, IH, J= 2.0 Hz), 8.27 (s, IH), 8.12 (s, 2H), 7.97 (d, IH, J= 8.9 Hz), 7.81 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.77 (s, IH), 6.55 (t, IH, J= 5.0 Hz), 6.37 (s, IH), 3.96 (br s, 2H), 3.50 (t, 2H, J= 5.6 Hz), 3.15 (q, 4H, J= 6.1 Hz), 2.77 (t, 4H, J= 5.6 Hz), 2.67 (t, 2H, J= 7.0 Hz), 1.57 (br s, 4H), 1.47 (br s, 4H). LC/MS: m/z 517.14 [MH⁺] (40), t_κ = 1.94 min (ZQ2000, polar_5min). [510] EXAMPLE 180: 4-[4-(BenzothiazoI-6-ylamino)-7H-pyrroIo[2,3-rf]- pyrimidm-6-yl]-3,6-dihydro-2/?-pyridine-l-carboxylic acid [2-(4-hydroxypiperidin-l-yl)- ethyl] -amide.

[511] Following the general procedure, the title compound was isolated as yellow powder. ¹HNMR (400 MHz, DMSO-d₆): δ = 11.92 (s, IH), 9.53 (s, IH), 9.17 (s, IH), 8.85 (d, IH, J= 2.0 Hz), 8.28 (s, IH), 8.13 (s, 2H), 7.97 (d, IH, J= 8.9 Hz), 7.81 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.77 (s, IH), 6.58 (t, IH, J= 5.0 Hz), 6.38 (s, IH), 3.96 (br s, 2H), 3.50 (t, 4H, J= 5.3 Hz), 3.17 (q, 2H, J= 5.8 Hz), 2.86 (q, 2H, J= 6.0 Hz), 2.55 (t, 2H, J= 6.6 Hz), 2.42 (br s, 2H), 2.36 (m, IH), 1.70 (m, 2H), 1.40 (m, 2H). LC/MS: m/z 519.14 [MH⁺] (30), t_κ = 1.80 min (ZQ2000, polar_5nύn).

[512] EXAMPLE 181: 4-[4-(Benzothiazol-6-yIamino)-7H~pyrroIo[2,3-<f]- pyrimidin-6~yl]-3,6-dihydro-2//-pyridine-l-carboxyIic acid [2-(4-isopropyIpiperazin-l- yl)-ethyl] -amide.

[513] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSOd₆): δ = 11.92 (s, IH), 9.53 (s, IH), 9.17 (s, IH), 8.85 (d, IH, J= 2.0 Hz), 8.27 (s, IH), 8.12 (s, 2H), 7.97 (d, IH, J= 8.9 Hz), 7.81 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.77 (s, IH), 6.43 (t, IH, J= 5.3 Hz), 6.37 (s, IH), 3.95 (br s, 4H), 3.48 (t, 4H, J= 5.6 Hz), 3.12 (q, 4H, J= 6.3 Hz), 2.64 (m, IH), 2.52 (br s, 2H), 2.41 (m, 2H), 2.33 (t, 2H, J= 7.3 Hz), 0.91 (d, 6H, J= 6.6 Hz). LC/MS: m/z 546.20 [MH⁺] (20), t_κ= 1.80 min (ZQ2000, polar_5min).

[514] EXAMPLE 182: 4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxyIic acid [2-(4,4-difluoropiperidin-l- yl)-ethyl] -amide.

[515] Following the general procedure, but using 4,4-difluoropiperidine hydrochloride and an additional 2eq. of N,N-diisopropylethylamine, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSOd₆): δ = 11.92 (s, IH), 9.52 (s, IH), 9.17 (s, IH), 8.85 (d, IH, J= 2.0 Hz), 8.28 (s, IH), 8.02 (s, 2H), 7.97 (d, IH, J= 8.9 Hz), 7.81 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.77 (s, IH), 6.43 (t, IH, J= 5.3 Hz), 6.37 (s, IH), 3.95 (br s, 2H), 3.49 (t, 2H, J= 5.3 Hz), 3.11 (q, 4H, J= 6.3 Hz), 2.52 (br s, 2H), 2.38 (t, 4H, J= 7.1 Hz), 1.86 (m, 4H). LC/MS: in/z 539.08 [MH⁺] (40), t_κ = 1.94 min (ZQ2000, polar_5min). [516] EXAMPLE 183: 4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2/Z-pyridine-l-carboxylic acid [2~(3,5-dimethylpiperazin-l- yl)-ethyl] -amide.

[517] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSOd₆): δ = 11.93 (s, IH), 9.55 (s, IH), 9.17 (s, IH), 8.85

(d, IH, J= 2.0 Hz), 8.28 (s, IH), 8.11 (s, 2H), 7.97 (d, IH, J= 8.9 Hz), 7.81 (dd, IH, J= 2.0

Hz & 8.9 Hz), 6.77 (s, IH), 6.42 (t, IH, J= 5.2 Hz), 6.37 (s, IH), 3.94 (br s, 2H), 3.49 (t, 2H,

J= 5.6 Hz), 3.11 (q, 2H, J= 6.3 Hz), 3.00 (m, 2H), 2.85 (m, 2H), 2.41 (br s, 2H), 2.33 (t, 2H,

J= 6.8 Hz), 1.76 (t, 2H, J= 11.4 Hz), 1.03 (d, 6H, J= 6.3 Hz). LC/MS: m/∑ 532.15 [MH⁺]

(60), t_R = 1.77 min (ZQ2000, polar_5min).

[518] General procedure for 3-aminopropyl derivatives:

[519] To a solution of benzothiazol-6-yl-[6-(l,2,3,6-tetrahydropyridin-4-yl)-7H- pyrrolo[2,3-(f|pyrimidin-4-yl]-amine tris-hydrochloride (65.3mg) in DMF (4mL) at rt were added N,N-diisopropylethylamine (5eq.) followed by l-chloro-3-iodopropane (30.0mg). The resulting mixture was left at rt for 5d. To this solution, containing benzothiazol-6-yl-{6-[l-

(3-chloropropyl)-l,2,3,64e1xahydropyridin-4-yl]-7H-pyrrolo[2,3-J]pyrirnidin-4-yl}-amrne, divided into 2 aliquots, were added lmg of KI, 5eq. NN-diisopropylethylamine, and 5eq. of the corresponding amine. The above solutions were degassed with N₂ and heated at 60⁰C for

2d. The products were purified by preparative HPLC with water / acetonitrile / formic acid mixtures and are assumed to be formate salts.

[520] EXAMPLE 184: BenzothiazoI-6-yl-{6-[l-(3-chIoropropyl)-l,2,3,6- tetrahydropyridin-4-yI] -T/f-pyrrolo [2,3-rf] pyrimidin-4-yI}-amine.

[521] LC/MS: m/z 424.95 [MH⁺] (20), f_R = 1.86 min (ZQ2000, polar_5min). [522] EXAMPLE 185: Benzothiazol-6-yl-(6-{l-[3-(4-methylpiperazin-l-yI)- propyI]-l,2,3,6-tetrahydropyridin-4-yl}-7J3-pyrrolo[2,3-rf]pyrimidin-4-yI)-amine.

[523] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.94 (s, IH), 9.56 (s, IH), 9.19 (s, IH), 8.85 (d, IH, J= 2.0 Hz), 8.29 (s, IH), 8.08 (s, 2H), 7.97 (d, IH, J= 8.9 Hz), 7.80 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.72 (d, IH), 6.29 (s, IH), 3.21 (br s, 4H), 2.81 (t, 2H, J= 6.9 Hz), 2.66 (m, 4H), 2.56 (t, 2H, J= 7.4 Hz), 2.52 (m, 4H), 2.36 (s, 3H), 1.69 (m, 2H). LC/MS: m/z 489.03 [MH⁺] (20), t_κ = 1.53 min (ZQ2000, polar_5min).

[524] EXAMPLE 186: BenzothiazoI-6-yl-{6-[l-(3-piperidin-l-ylpropyl)- l,2,3,6-tetrahydropyridin-4-yl]-7iϊ-pyrrolo[2,3-rf]pyrimidin-4-yl}-amme.

[525] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.91 (s, IH), 9.55 (s, IH), 9.16 (s, IH), 8.84 (d, IH, J= 2.0 Hz), 8.27 (s, IH), 8.08 (s, 2H), 7.97 (d, IH, J= 8.9 Hz), 7.65 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.74 (d, IH), 6.32 (s, IH), 3.20 (br s, 2H), 3.03 (br s, 4H), 2.90 (t, 2H_; J= 7.6 Hz), 2.67 (t, 2H, J= 5.6 Hz), 2.52 (m, 4H), 1.79 (m, 2H), 1.59 (m, 4H), 1.44 (m, 2H). LC/MS: m/z 474.04 [MH⁺] (30), t_R = 1.55 min (ZQ2000, polar_5min). [526] EXAMPLE 187: 4-[4-(l-Ethyl-l#-pyrazol-4-ylamino)-7H-pyrroIo[2,3- d]pyrimidin-6-yI]-3,6-dihydro-2J?-pyridine-l-carboxylic acid tert-butyl ester.

[527] A mixture

pyridine-1-carboxylic acid tert-butyl ester (HOmg, 0.33mmol) and l-ethyl-4-amino-lH- pyrazole (44mg, 0.39mmol) in 1-butanol (3mL) was heated at 120⁰C overnight, LC-MS showed the desired product and some de-Boc product. After the mixture was cooled to rt, it was diluted with methylene chloride (3mL), then NJV-diisopropylethylamine (0.1 ImL, 0.66mmol) and di-tert-butyldicarbonate (72mg, 0.33mmol) were added, the resulting mixture was stirred at rt for 30min. The mixture was diluted with EtOAc (3OmL), then washed with brine (2OmL), and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was crystallized with EtOAc to give the title compound as an off-white solid. LC-MS (ES, Pos.): 410 [MH⁺]. ¹HNMR (CDCl₃, 400 MHz): δ = 1.51 (s, 9H), 1.56 (t, J = 7.3 Hz, 3H), 2.50 (m, 2H), 3.66 (m, 2H), 4.16 (m, 2H), 4.22 (q, J = 7.3 Hz, 2H), 6.04 (s, IH), 6.17 (s, IH), 6.57 (s, IH), 7.56 (s, IH), 7.95 (s, IH), 8.38 (s, IH), 10.96 (br s, IH). [528] 4-Amino-l-ethyl-lfi-pyrazole

[529] To a solution of l-ethyl-4-nitro-lH-pyrazole (59mg, 0.42mmol) in ethyl acetate (2mL) and ethanol (2mL) was added 10% Pd-C (20mg), and the resulting mixture was stirred under hydrogen atmosphere overnight. TLC showed the reaction was complete. The catalyst was removed by filtration through a pad of celite, and the filtrate was concentrated under reduced pressure to give the title compound as red oil. ¹H NMR (CDCl₃, 400 MHz): δ = 1.43 (t, J= 7.3 Hz, 3H), 2.90 (br s, 2H), 4.05 (q, J= 7.3 Hz, 2H), 7.02 (d, J= 0.8 Hz, IH), 7.15 (d, J= 0.8 Hz, IH). [530] l-EthyI-4-nitro-lH-pyrazole

[531] To a solution of 4-nitro-l/f-pyrazole (226mg, 2.0mmol) in N,N- dimethylformamide (3mL) were added potassium carbonate (0.33g, 2.4mmol) and iodoethane (0.37g, 2.4mmol). The resulting mixture was stirred at rt overnight. TLC showed the reaction was complete. The mixture was diluted with EtOAc (4OmL), then washed with water (2 x 2OmL), brine (2OmL), and dried over anhydrous sodium sulfate. The crude material was purified by chromatography on silica gel, eluting with Hex:EtOAc = 70:30 to give the title compound as a white solid. ¹H ΝMR (CDCl₃, 400 MHz): δ = 1.55 (t, J= 7.3 Hz, 3H), 4.22 (q, J= 7.3 Hz, 2H), 8.07 (s, IH), 8.14 (s, IH).

[532] EXAMPLE 188: 4-[4-(l-Phenethyl-lH-pyrazoI-3-ylamino)-7H- pyrroloβjS-^pyrimidin-ό-yll-Sjό-dihydro-lH-pyridine-l-carboxylic acid tert-butyl ester.

[533] A mixture of 4-(4-chloro-7H-pyrrolo[2,3-cTlpyrimidin-6-yl)-3 ,6-dihydro-2H- pyridine-1-carboxylic acid tert-butyl ester (HOmg, 0.33mmol) and 3-amino-l-phenethyl-lH- pyrazole (74mg, 0.39mmol) in 1-butanol (3mL) was heated at 120⁰C overnight, LC-MS showed the reaction was complete. The mixture was concentrated, then dissolved in MeOH- DMSO, and purified by MSDP (using water / acetonitrile / HCOOH mixtures) to give the title compound as a brown solid. LC-MS (ES, Pos.): 486 [MH⁺]. ¹H NMR (CD₃OD, 400 MHz): δ = 1.49 (s, 9H), 2.54 (m, 2H), 3.16 (t, J= 7.1 Hz, 2H), 3.65 (m, 2H), 4.12 (m, 2H), 4.32 (t, J= 7.1 Hz, 2H), 6.27 (s, IH), 6.48 (d, J= 2.3 Hz, IH), 6.53 (s, IH), 7.14-7.28 (m, 5H), 7.36 (d, J = 2.3 Hz, IH), 8.21 (s, IH). [534] 3-Amino-l-phenethyI-liϊ-pyrazole

[535] To a solution of 3-nitro-l-phenethyl-lH-pyrazole (90mg, 0.41mmol) in ethyl acetate (2mL) and ethanol (2mL) was added 10% Pd-C (20mg), the resulting mixture was stirred under hydrogen atmosphere overnight. TLC showed the reaction was complete. The catalyst was removed by filtration through a pad of celite, and the filtrate was concentrated under reduced pressure to give the title compound as colorless oil. LC-MS (ES, Pos.): 188 [MH⁺]. ¹H NMR (CDCl₃, 400 MHz): δ = 3.10 (t, J= 7.2 Hz, 2H), 3.64 (br s, 2H), 4.12 (t, J= 7.2 Hz, 2H), 5.51 (d, J= 2.3 Hz, IH), 6.91 (d, J= 2.3 Hz, IH), 7.08-7.11 (m, 2H), 7.20-7.30 (m, 3H). [536] 3-Nitro-l-phenethyl-lF-pyrazole

O₂N _N_S _ ^ //

[537] To a solution of 3-nitro-lH-pyrazole (226mg, 2.0mmol) in NN- dimethylformamide (3mL) were added potassium carbonate (0.33g, 2.4mmol) and 1-bromo- 2-phenylethane (0.44g, 2.4mmol). The resulting mixture was stirred at rt overnight. TLC showed the reaction was complete. The mixture was diluted with EtOAc (4OmL), then washed with water (2 x 2OmL), brine (2OmL), and dried over anhydrous sodium sulfate. The crude material was purified by chromatography on silica gel, eluting with Hex:EtOAc = 80:20 → 70:30 to give the title compound as a white solid. ΝOE experiment confirmed the structure. ¹H ΝMR (CDCl₃, 400 MHz): δ = 3.22 (t, J= 7.1 Hz, 2H), 4.43 (t, J= 7.1 Hz, 2H), 6.79 (d, J= 2.5 Hz, IH), 7.06-7.09 (m, 2H), 7.12 (d, J= 2.5 Hz, IH), 7.23-7.32 (m, 3H). [538] 3-Νitro-lH-pyrazole

O₂N^%H

W

[539] [Ref.: Janssen, J.W.A.M. and Habraken, C.L., J. Org. Chem., 1971, 36,

3081.] A solution of 1-nitro-lH-pyrazole (3.Og, 0.026 mol) in anisole (20OmL) was heated at 145⁰C overnight. The mixture was cooled to rt, the white solid was collected by filtration and washed with hexanes. The mother liquid was diluted with hexanes (50OmL) and cooled to - 20⁰C, and the resulting off-white solid was collected and combined with the previous solid.

LC-MS (ES, Pos.): 114 [MH⁺]. ¹H NMR (DMSO-d₆, 400 MHz): δ = 7.04 (d, J= 2.5 Hz, IH),

8.04 (d, /= 2.5 Hz, IH), 13.96 (br s, IH).

[540] EXAMPLE 189: 4-[4-(l-Phenethyl-l#-pyrazol-4-ylamiαo)-7Jϊ- pyrrolo [2,3-rf] pyrimidin-6-yl] -3 ,6-dihydro-2fi-pyridine-l-carboxyIic acid tert-butyl ester.

[541] A mixture of 4-(4-chloro-7H-pyrrolo[2,3 -d]pyrimidin-6-yl)-3 ,6-dihydro-2H- pyridine-1-carboxylic acid tert-bvftyl ester (HOmg, 0.33mmol) and 4-amino-l-phenethyl-lH- pyrazole (74mg, 0.39mmol) in 1-butanol (3mL) was heated at 12O⁰C overnight, LC-MS showed the desired product and some de-Boc product (ca. 1 : 1 ratio). After the mixture was cooled to rt, it was diluted with methylene chloride (3mL), then N,N-diisopropylethylamine (0.1 ImL, 0.66mmol) and di-tert-butyldicarbonate (72mg, 0.33mmol) were added, the resulting mixture was stirred at rt for 30min. The mixture was diluted with EtOAc (3OmL), then washed with brine (2OmL), and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was crystallized with EtOAc to give the title compound as an off-white solid. LC-MS (ES, Pos.): 486 [MH⁺]. ¹H ΝMR (CDCl₃, 400 MHz): δ = 1.50 (s, 9H), 2.50 (m, 2H), 3.23 (t, J= 7.3 Hz, 2H), 3.66 (m, 2H), 4.17 (m, 2H), 4.38 (t, J= 7.3 Hz, 2H), 6.08 (s, IH), 6.17 (s, IH), 6.55 (s, IH), 7.17-7.32 (m, 5H), 7.60 (s, IH), 7.80 (s, IH), 8.37 (s, IH), 10.99 (br s, IH). [542] 4-Amino-l-phenethyl-ljff-pyrazole

[543] To a solution of 4-nitro-l-phenethyl-lH-pyrazole (90mg, 0.41mmol) in ethyl acetate (2mL) and ethanol (2mL) was added 10% Pd-C (20mg), and the resulting mixture was stirred under hydrogen atmosphere overnight. TLC showed the reaction was complete. The catalyst was removed by filtration through a pad of celite, and the filtrate was concentrated under reduced pressure to give the title compound as red oil. ¹H NMR (CDCl₃, 400 MHz): δ = 2.36 (br s, 2H), 3.11 (t, J= 7.5 Hz, 2H), 4.21 (t, J= 7.5 Hz, 2H), 6.83 (d, J= 0.8 Hz, IH), 7.10-7.12 (m, 2H), 7.18 (d, J= 0.8 Hz, IH), 7.20-7.28 (m, 3H). [544] 4-Nitro-l-phenethyl-lH-pyrazole

[545] To a solution of 4-nitro-lH-pyrazole (226mg, 2.0mmol) in NN- dimethylformamide (3mL) were added potassium carbonate (0.33g, 2.4mmol) and 1-bromo- 2-phenylethane (0.44g, 2.4mmol). The resulting mixture was stirred at rt overnight. TLC showed the reaction was complete. The mixture was diluted with EtOAc (4OmL), then washed with water (2 x 2OmL), brine (2OmL), and dried over anhydrous sodium sulfate. The crude material was purified by chromatography on silica gel, eluting with Hex:EtOAc = 80:20 → 70:30 to give the title compound as a white solid. ¹H ΝMR (CDCl₃, 400 MHz): δ = 3.20 (t, J= 7.0 Hz, 2H), 4.37 (t, J= 7.0 Hz, 2H), 7.04-7.07 (m, 2H), 7.25-7.32 (m, 3H), 7.81 (s, IH), 8.09 (s, IH). [546] 4-Νitro-lJ3-pyrazoIe

[547] [Ref: Huettel, R. and Buechele, F., Chem. Ber, 1955, 88, 1586-1590] 1-

Nitro-lH-pyrazole (2.2g, 0.019 mol) was dissolved in sulfuric acid (1OmL) at -10⁰C, and the resulting mixture was slowly warmed to rt overnight. The solution was added to ice (10Og) dropwise, and the resulting white solid was collected by filtration and washed with water. The aqueous phase was extracted with EtOAc (3x30mL), the combined organic phases were washed with brine (2x30mL), and dried over anhydrous sodium sulfate. Evaporation under reduced pressure provided an off-white solid, which was combined with the first solid and dried in vacuo to provide the title compound. LC-MS (ES, Pos.): 114 [MH⁺]. ¹H NMR (DMSO-d₆, 400 MHz): δ = 8.27 (s, IH), 8.90 (s, IH), 13.96 (br s, IH). [548] EXAMPLE 190: 4-[4-(Biphenyl-3-yIamino)-7H-pyrrolo[2,3-^pyrimidin-

6-yI]-3,6-dihydro-2jH-pyridine-l-carboxylic acid tert-butyl ester.

[549] A mixture of 4-(4-chloro-7H-pyrrolo[2,3 -d]pyrimidin-6-yl)-3 ,6-diliydro-2H- pyridine-1-carboxylic acid tert-butyl ester (60.0mg, 0.179mmol) andbiphenyl-3-ylamine (30.5mmol, 0.180mmol) in «BuOH (3mL) was heated to 8O⁰C (bath temp.) for 17h. The solvent was evaporated, water/NaHCO₃ solution was added, the mixture was extracted with CH₂Cl₂ (3x20mL), and the combined extracts were washed with brine and dried over MgSO₄. MgSO₄ was filtered off, the filtrate was concentrated, and the residue was chromatographed on silica gel [Jones Flashmaster, 5g / 25mL cartridge, eluting with CH₂Cl₂ (1-9) → 1% MeOH in CH₂Cl₂ (10-19) → 2% MeOH in CH₂Cl₂ (20-30)]. Fr.17-26 were combined and dried in vacuo overnight. One obtained the title compound as off-white solid. MS (ES+): m/z 468.1 (100) [MH⁺]. HPLC: t_R = 3.2 min (ZQ2000, nonpolar_5min). ¹H NMR (CDCl₃, 400 MHz): δ = 1.50 (s, 9H), 2.44-2.55 (brs, 2H), 3.61-3.71 (m,, 2H), 4.13-4.22 (m, 2H), 6.15 (s, IH), 6.24 (s, IH), 7.11 (brs, IH), 7.37 (t, J= 7.4 Hz, IH), 7.40-7.52 (m, 4H), 7.60-7.67 (m, 3H), 7.80 (t, J= 1.6 Hz, IH), 8.43 (s, IH), 11.83 (brs, IH).

[550] EXAMPLE 191: 4-[4-(3-Chloro-12J-indazoI-5-ylamino)-7H-pyrrolo[2,3- rf]pyrimidin-6-yl]-3,6-dihydro-2Jϊ-pyridine-l-carboxylic acid tert-butyl ester.

[551] A mixture of 4-(4-chloro-7H-pyrrolo[2,3-rf]pyrimidin-6-yl)-3,6-dihydro-2H- pyridine-1-carboxylic acid tert-butyl ester (49.6mg, 0.148mmol) and 5-amino-3- chloroindazole (26.5mg, 0.155mmol) in isopropyl alcohol (2.5mL, 0.033 mol) in a sealed tube was heated to 9O⁰C (bath temp.) for 3.5h. The bath temperature was increased to 105⁰C, and heating was continued overnight. The bath temperature was increased to 12O⁰C, and heating was continued for 5d. LC/MS at that time indicated loss of Boc group, i.e., (3-chloro- lH-indazol-5-yl)46-(l,2,3,6-tetrahydropyridin-4-yl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl]- amine, C₁₈H₁₆ClN₇, MW = 365.83. Solvents were evaporated. The reddish residue was suspended in NN-dimethylformamide (3mL). N,N-diisopropylethylarnine (52 μL, 0.30mmol) and di-tert-butyldicarbonate (33mg, 0.15mmol) were added, and the mixture was stirred at rt for 2h. DMF was evaporated, water and CH₂Cl₂ were added, and the insoluble brown material was filtered off and washed with CH₂Cl₂ and water. The layers of the filtrate were separated; the organic layer was washed with water (2x) and brine and dried over MgSO₄. The drying agent was filtered off, and the filtrate was concentrated, redissolved in MeOH, passed a through 0.45μm filter, and purified by MDP. One obtained the title compound as light tan solid. MS (ES+): m/z 465.9/467.9 (100/38) [MH⁺]. HPLC: t_κ = 2.7 min (ZQ2000, polar_5min). ¹H ΝMR (DMSO-J₆, 400 MHz): δ = 1.43 (s, 9H), 2.37-2.44 (brs, 2H), 3.51- 3.58 K, 2H), 3.99^.07 (m, 2H), 6.36 (s, IH), 6.54 (s, IH), 7.49 (d, J- 8.8 Hz, IH), 7.55 (d, J= 8.8 Hz, IH), 8.05 (s, IH), 8.12 (s, IH), 9.21 (s, IH), 11.88 (brs, IH), 13.43 (brs, IH). [552] Alternative synthesis: To a suspension of (3-chloro-lH-indazol-5-yl)-[6-

(l,2,3,6-tetrahydropyridm-4-yl)-7H-pyrrolo[2,3-J]pyrimidin-4-yl]-amine trifluoroacetate (179.8mg, 0.2457mmol, leq) and ώ-teπt-butyldicarbonate (63.1mg, 0.286mmol, 1.16eq) in anhydrous DCM (3mL), Ηϋnig's base (300 μL, 2mmol, 7eq) was added. Addition of anhydrous DMF (ImL) aided solubility. The reaction was stirred at rt for 2h and concentrated in vacuo. The crude material was adsorbed onto Ηydromatrix, dry loaded, and purified by chromatography on silica gel [Jones Flashmaster, 1Og / 7OmL cartridge, eluting with MeOH:DCM 1% -> 2% -» 5% → 7%]. Fractions 35-53 were combined and concentrated in vacuo. The material was purified on the Mass Directed Purification System (MDPS), yielding the title compound as a white solid. ¹H NMR (400 MHz, MeOH-^): δ = 1.50 (s, 9H), 2.49 (s, br, 2H), 3.64 (s, br, 2H), 4.12 (s, br, 2H), 6.27 (s, br, IH), 6.39 (s, br, IH), 7.56 (s, 2H), 8.06 (s, IH), 8.14 (s, IH). MS (ES+): m/z 465.95/467.97 [MH⁺]. HPLC: fe = 2.67 min (ZQ2000, polar_5min).

[553] (3-Chloro-lH-indazoI-5-yl)-[6-(l,2,3,6-tetrahydropyridin-4-yl)-7_JH- pyrrolo[2,3-rflpyrimidin-4-yI]-amine trifluoroacetate

[554] Into a 1OmL sealed tube, to a suspension / solution of 4-(4-chloro-7H- pyrrolo[2,3-^pyrimidin-6-yl)-3,6-dihydro-2H-pyridine-l-carboxylic acid ter^-butyl ester (85.3mg, 0.229mmol, leq) and 5-amino-3-chloroindazole (3) (43.3mg, 0.258mmol, 1.13eq) in 2,2,2-trifluoroethanol (TFE) (6mL), trifluoroacetic acid (TFA) (88//L, l.lmmol, 5eq) was added and the reaction was allowed to stir for 5d at 100⁰C. The reaction was cooled to rt and concentrated under reduced pressure. Purification of the crude material most likely to have been problematic- N-BOC protection carried out for easier purification by chromatography on silica gel. MS (ES+): /^ 365.98/367.98 (30/1O) [MH⁺]. HPLC: fe = 0.48 & 1.57 min (ZQ2000, polarjmin). [555] 5-amino-3-chloroindazole

[556] A mixture of 5-aminoindazole (1.373g, lO.OOmmol) and N-chlorosuccinimide

(1.381g, 10.14mmol) in methylene chloride (5OmL) was sonicated at rt for 30min. The brown mixture was then stirred overnight at rt. The suspension was diluted with CH₂Cl₂ to «100mL, water and aq. K₂CO₃ solution were added, and the insoluble brown material was filtered off and washed with CH₂Cl₂ and water. The layers of the filtrate were separated; the organic layer was washed with water (3x) and brine and dried over MgSO₄. The dried solution was filtered through a pad of silica gel, washing with 5% MeOH in CH₂Cl₂ until no more product eluted as indicated by TLC. Concentrating and drying in vacuo gave the title compound as yellow solid. MS (ES+): m/z 168.2/170.2 (100/37) [MH⁺]. HPLC: t_R = 2.1 min (ZQ2000, polar_5min). ¹H ΝMR (CDCl₃, 400 MHz): δ = 5.06 (s, 2H), 6.96 (d, J= 8.5 Hz, IH), 7.27 (d, J= 8.5 Hz, IH), 7.78 (s, IH), 12.95 (brs, IH). [557] EXAMPLE 192: l-{4-[4-(3-Chloro-lH-indazoI-5-ylamino)-7H- pyrrolo[2,3-d]pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yl}-3-piperidin-l-yI-propaii-l- one.

[558] To a suspension of (3-chloro-lH-indazol-5-yl)-[6-(l,2,3,6-tetrahydropyridin-

4-yl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl]-amine fris-hydrochloride (46.9mg, 0.0967mmol, leq), 1-piperidinepropanoic acid (40.5mg, 0.255mmol, 2.6eq), N-(3-dimethylaminopropyl)- N-ethylcarbodiimide hydrochloride (EDC) (56.2mg, 0.293mmol, 3eq), and 1- hydroxybenzotriazole (ΗOBt) (13.9mg, 0.103mmol, leq) in anhydrous DMF (5mL), DiPEA (85μL, 0.48mmol, 5eq) was added under an atmosphere of N₂. The reaction was stirred at rt for 18h, after which all solvent was evaporated under reduced pressure. The crude material was adsorbed onto Ηydromatrix, dry loaded, and purified by chromatography on silica gel [Jones Flashmaster, 5g / 25mL cartridge, eluting with MeOΗ:DCM 5% → 7N NH₃/Me0H:DCM 2% → 5% -> 8% → 15%]. Fractions 25-39 were combined and concentrated in vacuo, yielding the desired amide, but which contained a considerable amount of l-(3-dimethylaminopropyl)-3-ethylurea. The yellow solid was triturated in hot MeOH / sonication, giving the title compound as an off-white solid. ¹H NMR (400 MHz, CDCl₃): δ = 1.26 (s, br, 2H), 1.63 (rr^, 4H), 2.37-2.56 (m, 6H), 2.56-2.68 (m, 2H), 2.68-2.80 (m, 2H), 3.68 & 3.76 (t, J= 5.6 Hz, rotamers, 2H), 4.22 & 4.25 (s, br, rotamers, 2H), 5.92 & 5.98 (s, rotamers, IH), 6.18 & 6.22 (s, br, rotamers, IH), 7.49 (d, J= 8.8 Hz, IH), 7.79 (dd, J= 8.8, 1.6 Hz, IH), 8.13 (s, IH), 8.26 (s, IH). MS (ES+): m/z 505.00/506.99 (27/10) [MH⁺]; m/z 407.96/409.98 (100/36) [MH⁺-C₆H₁₄N]. HPLC: t_R = 1.75 min (ZQ2000, polar_5min). [559] (3-Chloro-lH-indazol-5-yl)-[6-(l,2,3,6-tetrahydropyridin-4-yl)-7H- pyrrolo[2,3-rf]pyrimidin-4-yl]-amine ^rø-hydrochloride.

[560] A suspension of 4-[4-(3-chloro-lH-indazol-5-ylamino)-7H-pyrrolo[2,3- rf]pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester (45.4mg, 0.0945mmol, leq) in 4.0M of HCl in 1,4-dioxane (3.25mL, 140eq) was allowed to stir at rt for 2h. The reaction was concentrated in vacuo to dryness, affording the title compound, as a yellow solid. ¹H NMR (400 MHz, MeOH-^): δ = 2.83 (s, br, 2H), 3.52 (t, J= 6.0 Hz, 2H), 3.95 (s, br, 2H), 6.44 (s, IH), 6.83 (s, br, IH), 7.56 (d, J= 8.8 Hz, IH), 7.75 (dd, J= 8.8, 0.8

Hz, IH), 8.19 (s, IH), 8.28 (d, J= 0.8 Hz, IH). MS (ES+): m/z 365.98/368.00 (20/8) [MH⁺].

HPLC: t_R = 0.48 & 1.56 min (ZQ2000, polar_5min).

[561] General procedure for preparation of a 3,6-dihydro-2H-pyridin-l-yl- ethanone library:

[562] To a solution of benzothiazol-6-yl-[6-(l ,2,3,6-tetrahydropyridin-4-yl)-7H- pyrrolo[2,3-J]pyrimidin-4-yl]-amine tris-hydrochloride (525mg, 1.15mmol) in DMF (12mL) and dichloromethane (ImL) at 4°C was added NN-diisopropylethylamine (0.7g, 6.0mmol) followed by chloroacetyl chloride (130mg, 1.15mmol). The resulting solution was allowed to warm up to rt and stirred overnight. This solution containing l-{4-[4-(benzothiazol-6- ylamino)-7H-pyrrolo[2,3-J]pyrimidin-6-yl]-3 ,6-dihydro-2H-pyridin-l -yl} -2-chloroethanone was divided into 13 aliquots to synthesize a 13-membered library, and lmg of KI, 5eq.

DIPEA, and 5eq. of the amines were added. If the amines were used as salts, additional

DIPEA was used. The above solutions were degassed with N₂ and heated at 50⁰C for 12h.

The products were purified by preparative ΗPLC with water / acetonitrile / formic acid mixtures and are assumed to be formate salts.

[563] EXAMPLE 193: l-{4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yl}-2-chloroethanone.

[564] MS: m/z 424.9/426.9 (100/45) [MH⁺]; HPLC: t_R = 2.45 min (ZQ2000, polar_5min).

[565] EXAMPLE 194: l-{4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yI]-3,6-dihydro-2jH-pyridin-l-yl}-2-(4-methylpiperazin-l-yI)-ethanone.

[566] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSOd₆): δ = 11.96 (d, IH, J= 10.3 Hz), 9.55 (br s, IH), 9.17 (s, IH), 8.85 (d, IH, J= 2.0 Hz), 8.27 (s, IH), 8.12 (s, 2H), 7.97 (d, IH, J= 8.9 Hz), 7.80 (dd, IH, J= 2.1 Hz & 8.9 Hz), 6.78 (IH, d), 6.37 (s, IH), 4.25 (s, IH), 4.08 (s, 2H), 3.68 (t, IH, J= 5.4 Hz), 3.64 (t, IH, J= 5.4 Hz), 3.18 (d, 2H, J= 6.4 Hz), 2.53 (br s, 2H), 2.41 (m, 7H), 2.16 (s, 3H). MS: m/z 489.04 (35) [MH⁺]. HPLC: t_R = 1.81 min (ZQ2000, polar_5min). [567] EXAMPLE 195: l-{4-[4-(BenzothiazoI-6-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yI}-2-pyrroIidin-l-yIethanone.

[568] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSOd₆): δ = 11.96 (d, IH, J= 17.2 Hz), 9.55 (d, IH, J= 5.3 Hz), 9.17 (s, IH), 8.90 (s, IH), 8.26 (s, IH), 8.13 (s, 2H), 7.97 (d, IH, J= 8.9 Hz), 7.80 (d, IH, J= 8.9 Hz), 6.78 (d, IH, J= 8.9 Hz), 6.37 (d, IH, J= 3.1 Hz), 4.21 (s, IH), 4.09 (s, IH), 3.66 (t, 2H, J= 5.4 Hz), 3.48 (d, 2H, J= 6.2 Hz), 2.60 (m, 5H), 2.51 (br s, IH), 1.68 (d, 4H, J = 2.5 Hz). MS: rø/z 460.02 (70) [MH⁺]. HPLC: t_κ = 1.82 min (ZQ2000, polar_5min). [569] EXAMPLE 196: l-{4-[4-(Benzothiazol-6-ylamino)-7#-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yI}-2-diethylaminoethanone.

[570] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.98 (d, IH, J= 15.8 Hz), 9.54 (d, IH, J= 12.7 Hz), 9.18 (s, IH), 8.85 (d, IH, J= 2.0 Hz), 8.24 (s, IH), 8.12 (s, 2H), 7.97 (d, IH, J= 8.9 Hz), 7.82 (d, IH, J= 8.9 Hz), 6.79 (d, IH), 6.34 (s, IH), 4.27 (s, IH), 4.15 (s, IH), 3.68 (m, 2H), 3.46 (d, 2H, J= 11.1 Hz), 2.53 (m, 6H), 0.96 (t, 6H, J= 7.1 Hz). MS: m/z 462.04 (80) [MH⁺]. HPLC: t_κ = 1.84 min (ZQ2000, polar_5min).

[571] EXAMPLE 197: l-{4-[4-(Benzothiazol-6-ylamino)-7S-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yl}-2-piperidin-l-yIethanone.

[572] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.95 (d, IH, J= 19.3 Hz), 9.50 (br s, IH), 9.13 (s, IH), 8.81 (s, IH, J= 2.0 Hz), 8.21 (s, IH), 8.08 (d, 2H), 8.00 (d, IH, J= 8.9 Hz), 7.78 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.75 (s, IH), 6.34 (s, IH), 4.22 (s, IH), 4.04 (s, IH), 3.65 (t, IH, J= 5.3 Hz), 3.60 (t, IH, J= 5.3 Hz), 3.17 (d, 2H, J= 7.9 Hz), 2.51 (br s, IH), 2.36 (m, 4H), 1.42 (m, 3H), 1.29 (m, 2H), 1.07 (d, 2H, J = 6.6 Hz). MS: m/z 474.04 (100) [MH⁺].

HPLC: t_R = 1.86 min (ZQ2000, polar_5min).

[573] EXAMPLE 198: l-{4-[4-(Benzothiazol-6-ylamino)-777-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2jH-pyridin-l-yl}-2-tert-butylaminoethanone.

[574] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): 5 = 11.99 (d, IH, J= 19.2 Hz), 9.63 (s, IH), 9.17 (s, IH), 8.84 (t, IH), 8.27 (d, IH, J= 2.7 Hz), 8.17 (s, 2H), 8.00 (d, IH, J= 8.8 Hz), 7.81 (dd, IH, J= 2.1 Hz & 8.8 Hz), 6.80 (d, IH₅ J= 7.9 Hz), 6.40 (br s, IH), 4.18 (s, IH), 4.13 (s, IH), 3.72 (m, 2H), 3.63 (t, IH, J= 5.4 Hz), 2.55 (br s, IH), 1.13 (s, 9H), 2.75 (br s, IH), 2.60 (m, 2H), 1.41 (s, 9H). MS: m/z 462.04 (80) [MH⁺]. HPLC: fc = 1.87 min (ZQ2000, polar_5min). [575] EXAMPLE 199: l-{4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2i?-pyridin-l-yI}-2-dimethylaminoethanone.

[576] Following the general procedure, but saturating the reaction solution with dimethylamine gas in a sealed tube and reacting it at rt for two days, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.94 (d, IH, J = 7.8 Hz), 9.53 (d, IH, J= 7.2 Hz), 9.21 (s, IH), 8.84 (s, IH), 8.27 (s, IH), 8.15 (s, 2H), 7.96 (d, IH, J= 8.9 Hz), 7.68 (dd, IH, J= 2.0 Hz & 8.9 Hz), 6.77 (d, IH, J= 6.4 Hz), 6.36 (d, IH, J= 3.5 Hz), 4.25 (br s, IH), 4.07 (br s, IH), 3.55 (m, 3H), 2.51 (br s, IH), 2.15 (d, 6H, J= 6.4 Hz). MS: m/z 434.00 (30) [MH⁺]. HPLC: t_R = 1.79 min (ZQ2000, polar_5min). [577] EXAMPLE 200: l-{4-[4-(BenzothiazoI-6-yIamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yl}-2-(3-hydroxypyrrolidin-l-yI)-ethanone.

[578] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.98 (d, IH, J= 18.3 Hz), 9.55 (s, IH), 9.16 (s, IH), 8.85 (d, IH, J= 1.7 Hz), 8.40 (s, IH), 8.14 (s, 2H), 7.94 (d, IH, J= 8.6 Hz), 7.81 (dd, IH₃ J= 1.9 Hz & 8.6 Hz), 6.78 (d, IH, J= 7.2 Hz), 6.21 (br s, IH), 4.21 (br s, IH), 4.14 (br s, IH), 4.08 (s, IH), 3.70 (m, 2H), 3.35 (m, 2H), 2.82 (m, 2H), 2.63 (m, 2H), 2.45 (m, IH), 2.42 (m, 2H), 1.88 (m, IH), 1.50 (m, IH). MS: m/z 476.00 (60) [MH⁺]. HPLC: t_R = 1.78 min (ZQ2000, polar_5min).

[579] EXAMPLE 201: 2-Azepan-l-yl-l-{4-[4-(benzothiazoI-6-ylamino)-7JΪ- pyrrolo [2,3-rf] py rimidin-6-yl] -3 ,6-dihydro-2H-py ridin-l-yl}-ethanone.

[580] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSOd₆): δ = 12.06 (s, IH), 9.54 (d, IH, J= 3.7 Hz), 9.17 (s, IH), 8.84 (d, IH, J= 2.0 Hz), 8.31 (s, IH), 8.12 (s, 2H), 7.97 (d, IH, J= 8.7 Hz), 7.80 (dd, IH, J= 2.0 Hz & 9.2 Hz), 6.78 (s, IH), 6.38 (s, IH), 4.27 (s, IH), 4.07 (s, IH), 3.69 (t, 2H, J = 5.6 Hz), 3.65 (t, IH, J= 5.6 Hz), 3.38 (s, 2H), 2.62 (m, 4H), 2.55 (m, IH), 1.50 (m, 8H). LC/MS: m/z 488.07 (25) [MH⁺], /_R = 1.91 min (ZQ2000, polar_5min). [581] EXAMPLE 202: l-{4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-rfl- pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yl}-2-(4-hydroxypiperidin-l-yl)-ethanone.

[582] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.97 (d, IH, J= 15.3 Hz), 9.53 (s, 1H), 9.16 (s, IH), 8.85 (s, IH), 8.27 (d, IH, J= 1.5 Hz), 8.09 (s, 2H), 7.97 (d, IH, J= 8.9 Hz), 7.81 (dd, IH, J= 1.5 Hz & 8.9 Hz), 6.79 (s, IH), 6.38 (s, IH), 4.22 (br s, IH), 4.09 (br s, IH), 3.66 (m, 2H), 3.44 (m, 2H), 3.36 (s, IH), 2.74 (m, 3H), 2.54 (m, IH), 2.35 (m, IH), 2.22 (m, 2H), 1.70 (m, 2H), 1.39 (m, 2H). LC/MS: m/z 490.03 (45) [MH⁺], /_R = 1.77 min (ZQ2000, polarjmin). [583] EXAMPLE 203: l-{4-[4-(Benzothiazol-6-ylamino)-7_JH^r-pyrroIo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2_JH^r-pyridin-l-yl}-2-(4-isopropylpiperazin-l-yl)-ethanone.

[584] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR ^OO MHz, DMSO-d₆): δ = 11.96 (d, IH, J= 19.8 Hz), 9.54 (d, IH, /= 4.6 Hz), 9.17 (s, IH), 8.85 (s, IH), 8.36 (s, IH), 8.10 (s, 2H), 7.97 (d, IH, J= 9.7 Hz), 7.80 (dd, IH, J= 2.0 Hz & 9.7 Hz), 6.75 (s, IH), 6.37 (br s, IH), 4.25 (br s, 2H), 4.15 (br s, 2H), 3.70 (t, 2H, J= 5.2 Hz), 3.62 (t, IH, J= 5.2 Hz), 3.18 (d, 4H, J= 6.4 Hz), 2.67 (m, 2H), 2.52 (m, 4H), 0.91 (d, 6H, J= 6.5 Hz). LC/MS: m/z 517.07 (95) [MH⁺], *_R = 1.84 min (ZQ2000, polar_5min).

[585] EXAMPLE 204: l-{4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yl}-2-morpholin-4-ylethanone.

[586] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSOd₆): δ = 11.98 (d, IH, J= 14.6 Hz), 9.61 (s, IH), 9.17 (s, IH), 8.85 (d, IH, ./= 2.0 Hz), 8.31 (s, IH), 8.11 (s, 2H), 7.97 (d, IH, J= 8.6 Hz), 7.81 (dd, IH, J= 2.0 Hz & 8.6 Hz), 6.78 (s, IH), 6.38 (br s, IH), 4.26 (br s, IH), 4.08 (br s, IH), 3.70 (t, 2H, J= 5.2 Hz), 3.62 (t, 2H, J= 5.2 Hz), 3.51 (m, 4H), 3.17 (d, 2H, J= 11.6 Hz), 2.52 (m, IH), 2.29 (br s, 3H). LC/MS: m/z 476.00 (95) [MH⁺], t_κ = 1.81 min (ZQ2000, polar_5min). [587] EXAMPLE 205: l-{4-[4-(Benzothiazol-6-yIammo)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yI}-2-(4,4-difluoropiperidin-l-yl)-ethanone.

[588] Following the general procedure, but using 4,4-difluoropiperidine hydrochloride and additional 2 equiv. of DIPEA, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.98 (d, IH, J= 14.3 Hz), 9.54 (d, IH, J= 3.6 Hz), 9.16 (s, IH), 8.85 (d, IH, J= 2.0 Hz), 8.27 (s, IH), 8.11 (s, 2H), 7.97 (d, IH, J= 8.8 Hz), 7.80 (dd, IH, J = 2.0 Hz & 8.8 Hz), 6.78 (s, IH), 6.32 (br s, IH), 4.22(br s, IH), 4.08 (br s, IH), 3.66 (t, 2H, J= 5.7 Hz), 3.54 (t, IH, J =5.7 Hz), 3.45 (m, IH), 3.27 (d, 2H, J= 9.5 Hz), 2.53 (br s, 4H), 1.87 (m, 4H). LC/MS: m/z 509.99 (40) [MH⁺], t_R = 1.98 min (ZQ2000, polar_5min).

[589] EXAMPLE 206: l-{4-[4-(Benzothiazol-6-yIamino)-7H-pyrroIo[2,3-<q- pyriraidin-6-yl]-3,6-dihydro-2H-pyridin-l-yI}-2-(3,5-dimethylpiperazin-l-yI)-ethanone.

[590] Following the general procedure, the title compound was isolated as yellow powder. Its structure has been confirmed by 2D ROESY NMR experiments. It's derived from cis/trans 2,6-dimethylpiperazine, with predominantly cis isomer. ¹H NMR (400 MHz, DMSOd₆): δ = 11.98 (d, IH, J= 17.2 Hz), 9.56 (s, IH), 9.16 (s, IH), 8.85 (d, IH, /= 2.1 Hz), 8.27 (s, IH), 8.20 (s, 2H), 7.96 (d, IH, J= 8.9 Hz), 7.75 (dd, IH, J= 2.1 Hz & 8.9 Hz), 6.78 (d, IH, J= 4.1 Hz), 6.36 (br s, IH), 4.20 (s, IH), 4.15 (s, IH), 3.64 (q, 2H, J= 5.5 Hz), 3.51 (s, 2H), 3.22 (br s, 2H), 2.97 (m, 2H), 2.73 (m, 2H), 2.51 (br s, IH), 1.91 (m, IH), 1.01 (m, 6H). LC/MS: m/z 503.05 (30) [MH⁺], t_R = 1.83 min (ZQ2000, polar_5min). [591] General procedure for preparation of a 3,6-dihydro-2H-pyridin-l-yl- propanone library:

[592] To a solution of benzothiazol-6-yl-[6-(l ,2,3,6-tetrahydropyridin-4-yl)~7H- pyrrolo[2,3-^pyrimidm-4-yl]-amine tris-hydrochloride (187mg, 0.408mmol) in DMF (l-2mL) and dichloromethane (ImL) at 4⁰C was added N,N-diisopropylethylamine (0.3g, 2.0mmol), followed by 3-chloropropanoyl chloride (52mg, 0.41mmol). The resulting mixture was allowed to warm up to rt and stirred overnight. This solution containing l-{4-[4- (benzothiazol-6-ylamino)-7H-pyrrolo[2,3 - J]pyrimidin-6-yl] -3 ,6-dihydro-2H-pyridin- 1 -yl} -3 - chloropropan-1-one and l-{4-[4-(benzo1liiazol-6-ylamino)-7H-pyrrolo[2,3-c(]pyrimidin-6-yl]- 3,6-dihydro-2H-pyridin-l-yl}-propenone was divided into 13 aliquots to synthesize a 13- membered library, and lmg of KI, 5eq. DIPEA, and 5eq. of the amines were added. If the amines were used as salts, additional DIPEA was used. The solutions were degassed with N₂ and heated at 7O⁰C for 48h. The products were purified by preparative ΗPLC with water / acetonitrile /formic acid mixture and are assumed to be formate salts. [593] EXAMPLE 207: l-{4-[4~(BenzothiazoI-6-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yl}-3-chIoropropan-l-one.

[594] ΗPLC purification of the reaction mixture gave the title compound as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.99 (d, IH, J= 17.2 Hz), 9.55 (s, IH), 9.17 (s, IH), 8.84 (s, IH), 8.28 (s, IH), 7.97 (d, IH, J= 8.9 Hz), 7.79 (d, IH, J= 11.8 Hz), 6.78 (IH, d, J= 6.3 Hz), 6.38 (s, IH), 4.18 (d, 2H, J= Yl 2 Hz), 3.81 (q, 2H, J= 6.6 Hz), 3.64 (m, 2H, J= 5.5 Hz), 2.90 (t, IH, J= 6.6 Hz), 2.84 (t, IH, J= 6.6 Hz), 2.51 (s, IH). LC/MS: m/fe

438.98/440.94 (100/40) [MH⁺], t_R = 2.52 min (ZQ2000, polar_5min).

[595] EXAMPLE 208: l-{4-[4-(BenzothiazoI-6-yIamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yI]-3,6-dihydro-2H-pyridin-l-yl}-propen(me.

[596] HPLC purification of the reaction mixture gave the title compound as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.96 (d, IH, J= 17.2 Hz), 9.55 (s, IH), 9.20 (s, IH), 9.16 (s, IH), 8.28 (d, 2H, J= 6.5 Hz), 7.97 (d, IH, J= 8.9 Hz), 7.81 (d, IH, J= 11.8 Hz), 6.88 (m, IH), 6.78 (m, IH), 6.38 (s, IH), 6.09 (d, IH, J= 16.2 Hz), 4.27 (s, IH), 4.16 (s, IH), 3.72 (m, 3H), 2.95 (t, IH, J= 6.6 Hz). LC/MS: m/z 402.98 (100) [MH⁺], t_R = 2.30 min (ZQ2000, polar_5min).

[597] EXAMPLE 209: l-{4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yI]-3,6-dihydro-2H-pyridin-l-yl}-3-(4-methyIpiperazin-l-yl)-propan-l-one.

[598] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 12.30 (IH, d, J= 17.2 Hz), 9.61 (s, IH), 9.27 (s, IH), 8.92 (s, IH), 8.34 (s, IH), 8.04 (d, IH, J= 8.9 Hz), 7.88 (d, IH₅ J= 8.9 Hz), 6.84 (IH, d, J= 6.4 Hz), 6.44 (s, IH), 4.24 (IH, s), 4.14 (IH, s), 3.77 (t, 2H, J= 6.6 Hz), 3.30 (m, 10H), 2.93 (s, IH, J= 6.6 Hz), 2.89 (s, IH), 2.74 (s, IH), 2.73 (d, IH, J= 0.5 Hz), 2.14 (t, 3H, J= 8.1 Hz). LC/MS: m/z 503.01 (30) [MH⁺], t_R = 1.79 min (ZQ2000, polar_5min). [599] EXAMPLE 210: l-{4-[4-(Benzothiazol-6-ylamino)-7H-pyrroIo[2,3-tf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yl}-3-pyrrolidin-l-ylpropan-l-one.

[600] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 12.34 (d, IH, J= 17.2 Hz), 9.61 (s, IH), 9.23 (s, IH), 8.91 (s, IH), 8.34 (s, IH), 8.03 (d, IH, J= 8.8 Hz), 7.87 (d, IH, J= 8.9 Hz), 6.84 (IH, d, J= 7.0 Hz), 6.44 (s, IH), 4.23 (IH, s), 4.13 (IH, s), 3.71 (t, 2H, J= 5.5 Hz), 3.32 (s, 6H), 2.60 (m, 3H), 2.14 (d, IH, J= 5.2 Hz), 1.66 (m, 4H). LC/MS: m/z 473.94 (70) [MH⁺], /_R =

1.82 min (ZQ2000, polar_5min).

[601] EXAMPLE 211: l-{4-[4-(Benzothiazol-6~ylamino)-7#-pyrrolo[2,3-d]~ pyrimidin-6-yI]-3,6-dihydro-2H-pyridin-l-yl}-3-diethyIaminopropan-l-one.

[602] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSOd₆): δ = 12.30 (d, IH, J= 17.2 Hz), 9.60 (s, IH), 9.24 (s, IH), 8.91 (s, IH), 8.34 (s, IH), 8.03 (d, IH, J= 8.9 Hz), 7.87 (d, IH, J= 8.9 Hz), 6.83 (d, IH, J= 6.4 Hz), 6.44 (s, IH), 4.24 (s, IH), 4.14 (s, IH), 3.71 (t, 2H, J= 5.5 Hz), 3.32 (s, 2H), 2.65 (m, 2H), 2.54 (br s, IH), 2.51 (m, IH), 2.47 (m, 4H), 0.93 (q, 6H, J= 7.90 Hz). LC/MS: m/z 475.96 (70) [MH⁺], t_R = 1.85 min (ZQ2000, polar_5min).

[603] EXAMPLE 212: l-{4-[4-(BenzothiazoI-6-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yl}-3-diisopropylaminopropan-l-one.

[604] The general procedure was followed, except that lOeq. of diisopropylamine were used and that the reaction was heated for 5d. LC/MS: m/z 504.04 (15) [MH⁺], t_κ = 1.91

(ZQ2000, polar_5min).

[605] EXAMPLE 213: l-{4-[4-(BenzothiazoI-6-ylamino)-7H-pyrroIo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yl}-3-tert-butylaminopropan-l-one.

[606] Following the general procedure, but using lOeq. of tert-butylamine, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 12.21 (d, IH, J= 17.2 Hz), 9.79 (s, IH), 9.41 (s, IH), 9.07 (d, IH, J= 2.0 Hz), 8.50 (d, IH, J= 1.5 Hz), 8.43 (s, 4H), 8.21 (d, IH, J= 5.7 Hz), 8.04 (dd, IH, J= 2.1 Hz & 8.8 Hz), 7.99 (d, IH, 1.5 Hz), 7.68 (br s, IH), 7.02 (d, IH, J= 4.8 Hz), 6.60 (br s, IH), 4.36 (IH, s), 3.94 (t, IH, J= 5.7 Hz), 3.83 (t, IH, J= 5.7 Hz), 3.21 (t, 2H, J= 6.3 Hz), 2.99 (t, IH, J= 10.8), 2.90 (s, IH, J= 10.8 Hz), 2.75 (br s, IH), 2.60 (m, 2H), 1.41 (s, 9H). LC/MS: m/z 476.00 (100) [MH⁺], t_κ = 1.89 min (ZQ2000, polar_5min). [607] EXAMPLE 214: 3-Azetidin-l-yl-l-{4-[4-(benzothiazol-6-ylamino)-7H- pyrrolo[2,3-rf]pyrimidin-6-yl]-3,6-dihydro-2jBr-pyridin-l-yl}-propau-l-one.

[608] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 12.01 (d, IH, J= 17.2 Hz), 9.85 (s, IH), 9.21 (s, IH), 8.90 (s, IH), 8.29 (d, IH, J= 1.0 Hz), 8.23 (s, 2H), 7.97 (d, IH, J= 5.7 Hz), 7.81 (dd, IH, J= 2.1 Hz & 8.8 Hz), 6.80 (d, IH, J= 5.4 Hz), 6.40 (br s, IH), 4.16 (d, IH, J= 10.1 Hz), 3.68 (t, IH, J= 5.1 Hz), 3.63 (t, IH, J= 4.9 Hz), 3.01 (t, IH, J= 8.3 Hz), 2.85 (m, 2H), 2.34 (t, 4H, J= 6.6 Hz), 2.13 (m, 2H), 2.09 (t, 2H, J= 4.2 Hz), 1.67 (t, 2H, J= 7.2 Hz). LC/MS: m/z 126.01 (100%), 320.02 (50%), 332.01 (90%) [MH⁺ - H₂NCOCH₂CH₂N(CH₂)₃], 390.98 (35) [MH⁺ - CH₂N(CH₂)₃ ⁺], *_R = 1.62 min (ZQ2000, polar_5min). [609] EXAMPLE 215: l-{4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2J3^:-pyridin-l-yl}-3-(3-hydroxypyrroIidin-l-yl)-propan-l- o lie.

[610] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.84 (d, IH, J= 14.3 Hz), 9.42 (s, IH), 9.03 (s, IH), 8.76 (s, IH), 8.15 (s, IH), 8.01 (s, 4H), 7.87 (d, IH, J= 8.6 Hz), 7.67 (dd, IH, J= 1.9 Hz &10.9 Hz), 6.65 (d, IH, J= 8.1 Hz), 6.21 (br s, IH), 4.09 (br s, 2H), 3.96 (br s, IH), 3.51 (m, 4H), 2.81 (m, IH), 2.75 (m, 2H), 2.54 (m, 3H), 2.44 (m, 3H), 2.11 (s, IH), 1.82 (m, IH). LC/MS: m/z 490.00 (50) [MH⁺], h = 1-79 min (ZQ2000, polar_5min). [611] EXAMPLE 216: 3-Azepan-l-yl-l-{4-[4-(benzothiazol-6-ylamino)-7H- pyrrolo[2,3-rf]pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yl}-propan-l-one.

[612] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 12.06 (d, IH, J= 16.8 Hz), 9.62 (s, IH), 9.24 (s, IH), 8.92 (s, IH), 8.35 (s, IH), 8.25 (s, 3H), 8.04 (d, IH, J= 8.7 Hz), 7.88 (d, IH, J= 9.2 Hz), 6.85 (d, IH, J= 5.1 Hz), 6.45 (s, IH), 4.91 (s, IH), 4.55 (s, IH), 3.74 (t, 2H, J= 9.6 Hz), 2.90 (m, 2H), 2.70 (m, 3H), 2.68 (m, IH), 1.57 (m, 12H). LC/MS: m/z 502.03 (10) [MH⁺], t_R

= 1.91 min (ZQ2000, polar_5min).

[613] EXAMPLE 217: l-{4-[4-(Benzothiazol-6-ylamino)-7fi-pyrroIo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2_JH-pyridin-l-yl}-3-(4-hydroxypiperidin-l-yI)-propan-l- one.

[614] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 12.00 (d, IH, J= 18.3 Hz), 9.61 (s, IH), 9.17

(s, IH), 8.85 (s, IH), 8.28 (d, IH, J = 1.5 Hz), 8.12 (s, 3H), 7.97 (d, IH, J= 8.9 Hz), 7.81 (dd,

IH, J= 2.1 Hz & 8.9 Hz), 6.77 (d, IH, J= 5.8 Hz), 6.37 (d, IH, J= 2.1 Hz), 4.30 (br s, IH),

4.17 (br s, IH), 3.63 (d, 2H, J= 3.9 Hz), 3.36 (m, IH), 2.78 (m, 4H), 2.59 (m, 4H), 2.54 (m,

2H), 2.20 (m, 2H), 1.66 (m, 2H). LC/MS: m/z 503.99 (20) [MH⁺], t_κ = 1.79 min (ZQ2000, polar_5min).

[615] EXAMPLE 218: l-{4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-rfl- pyrimidin-6-yl]-3,6-dihydro-2_JH^r-pyridin-l-yl}-3-(4-isopropylpiperazin-l-yl)-propan-l- one.

[616] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 12.07 (d, IH, J= 18.3 Hz), 9.63 (s, IH), 9.23 (s, IH), 8.92 (s, IH), 8.34 (s, IH), 8.19 (s, 2H), 8.04 (d, IH, J= 8.9 Hz), 7.78 (d, IH, J= 15.2 Hz), 6.84 (d, IH, J= 5.3 Hz), 6.45 (br s, IH), 4.27 (br s, 2H), 4.24 (br s, 2H), 3.78 (t, 6H, J= 5.9 Hz), 2.67 (m, IH), 2.58 (m, 8H), 0.97 (t, 6H, J= 6.2 Hz). LC/MS: m/z 531.04 (20) [MH⁺], /_R = 1.81 min (ZQ2000, polar_5min).

[617] EXAMPLE 219: l-{4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2iϊ-pyridin-l-yl}-3-morphoIin-4-ylpropan-l-one.

[618] Following the general procedure, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSOd₆): δ = 12.01 (d, IH, J= 14.6 Hz), 9.60 (s, IH), 9.17 (s, IH), 8.83 (s, IH), 8.28 (d, IH, J= 1.2 Hz), 8.11 (s, 2H), 7.99 (d, IH, J= 8.6 Hz), 7.81 (dd, IH, J= 1.7 Hz & 9.3 Hz), 6.77 (d, IH, J= 6.3 Hz), 6.38 (br s, IH), 4.20 (br s, IH), 3.99 (br s, IH), 3.63 (t, 4H, J= 5.2 Hz), 3.50 (t, 4H, J= 4.3 Hz), 2.52 (m, 4H), 2.27 (m, 4H). LC/MS: m/z 489.96 (70) [MH⁺], t_R = 1.81 min (ZQ2000, polarjmin).

[619] EXAMPLE 220: l-{4-[4-(Benzothiazol-6-ylamino)-7J3-pyrroIo[2,3-rf|- pyrimidin-6-yl]-3,6-dihydro-2Jϊ-pyridin-l-yl}-3-(4,4-difluoropiperidin-l-yl)-propan-l- one.

[620] Following the general procedure, but using 4,4-difluoropiperidine hydrochloride and additional 2 equiv. of DIPEA, the title compound was isolated as yellow powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.97 (d, IH, J= 14.3 Hz), 9.56 (s, 1H), 9.18 (s, IH), 8.86 (d, IH, J= 2.1 Hz), 8.27 (d, IH, J= 1.4 Hz), 8.11 (s, 2H), 7.97 (s, IH), 7.85 (dd, IH, J= 2.1 Hz & 8.9 Hz), 6.79 (d, IH, J= 6.3 Hz), 6.39 (br s, IH), 4.19 (br s, IH), 4.09 (br s, IH), 3.79 (t, 2H, J= 5.7 Hz), 3.41 (m, 6H), 2.48 (m, 2H), 1.92 (m, 6H). LC/MS: m/z 523.96 (30) [MH⁺], *_R = 1.93 min (ZQ2000, polar_5min).

[621] EXAMPLE 221: l-{4-[4-(Benzothiazol-6-ylamino)-7H-pyrroIo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yl}-3-(3,5-dimethylpiperazin-l-yl)-propan-l- one.

[622] Following the general procedure, the title compound was isolated as yellow powder. Its structure has been confirmed by 2D ROESY NMR experiments. It's derived from cis/tr-ans 2,6-dimethylpiperazine, with predominantly cis isomer. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.92 (d, IH, J= 17.2 Hz), 9.62 (s, IH), 9.08 (s, IH), 8.72 (s, IH), 8.08 (s, IH), 7.98 (d, 2H), 7.89 (d, IH, J= 8.9 Hz), 7.68 (d, IH, J= 8.9 Hz), 6.65 (IH, d, J= 5.4 Hz), 6.26 (s, IH), 4.05 (2H, s), 3.95 (2H, s), 3.51 (s, 4H), 2.76 (m, IH), 2.47 (s, IH), 2.43 (m, IH), 1.91 (br s, IH), 1.64 (br s, IH), 1.48 (m, 3H), 0.74 (t, 6H, J= 6.0 Hz). LC/MS: m/z 516.00 (30) [MH⁺], t_κ = 1.99 min (ZQ2000, polar_5min). [623] EXAMPLE 222: l-4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yl-3-piperidin-l-ylpropan-l-one.

[624] To a suspension/solution of benzothiazol-6-yl-[6-(l,2,3,6-tetrahydropyridin-

4-yl)-7H-pyrrolo[2,3-J]pyrimidin-4-yl]-aniine frzs-hydrochloride (100.9mg, 0.220mmol, leq), 1-piperidinepropanoic acid (87.9mg, 0.554mmol, 2.5eq), EDC (130.8mg, 0.682mmol, 3eq), and HOBt (30.3mg, 0.224mmol, leq) in anhydrous DMF (6mL), DiPEA (192 μL, 1.lmmol, 5eq) was added at rt, under an atmosphere of N₂. The reaction mixture was stirred at rt for 15h and was concentrated under reduced pressure. The residue was dissolved in a 5% MeOH : DCM mixture and washed with NaHCO₃ (Ix) and brine (Ix), dried over anhydrous Na₂Sθ₄, filtered, and concentrated in vacuo. The crude material was adsorbed onto Hydromatrix, dry loaded, and purified by chromatography on silica gel [Jones Flashmaster, 5g / 25mL cartridge, eluting with MeOH:DCM 5% → 10% → 7N NH₃/Me0H:DCM 5%]. Fractions containing product were combined and concentrated in vacuo. Further purification of the yellow solid thus obtained by trituration in hot DCM / sonication gave the title compound as light tan solid. ¹H NMR (400 MHz, MeOH-^): δ = 1.45-1.58 (s, br, 2H), 1.60-1.72 (m, 4H), 2.49-2.85 (m, 10H), 3.81 & 3.85 (t, J= 5.6 Hz, rotamers, 2H), 4.27 & 4.32 (s, br, rotamers, 2H), 6.34 (d, J= 1.2 Hz, IH), 6.74 & 6.76 (s, rotamers, IH), 7.78 & 7.80 (dd, J= 8.8, 2.8 Hz, rotamers, IH), 8.02 (d, J= 8.8 Hz, IH), 8.29 & 8.30 (s, rotamers, IH), 8.75 & 8.76 (d, J= 2.0 Hz, rotamers, IH), 9.13 (s, 1H).MS (ES+): m/z 487.97 (75) [MH⁺]. HPLC: t* = 1.89 min (ZQ2000, polar_5min).

[625] EXAMPLE 223: l-4-[4-(Benzothiazol-6-yIamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yI]-3,6-dihydro-2H-pyridin-l-yl-3-dimethylaminopropan-l-one.

[626] The title compound was obtained following the procedure for 1 -4-[4-

(benzotliiazol-6-ylamino)-7H-pyrrolo[2,3-d]pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yl-3- piperidin-1-ylpropan-l-one, using 3-dimethylaminopropionic acid, as brown solid. ¹H NMR (400 MHz, MeOH-φ): δ = 2.33 & 2.35 (s, rotamers, 6H), 2.62 (s, br, 2H), 2.67-2.73 (m, 4H), 3.83 & 3.86 (t, J= 5.6 Hz, rotamers, 2H), 4.29 & 4.33 (s, br, rotamers, 2H), 6.36 (d, J= 1.6 Hz, IH), 6.75 & 6.77 (s, rotamers, IH), 7.79 & 7.81 (dd, J= 8.8, 2.8 Hz, rotamers, IH), 8.04 (d, J= 8.8 Hz, IH), 8.31 & 8.32 (s, rotamers, IH), 8.77 & 8.78 (d, J= 2.0 Hz, rotamers, IH), 9.15 (s, IH). MS (ES+): m/z 448.00 (12) [MH⁺]. HPLC: fe = 2.00 min (ZQ2000, polar_5min).

[627] EXAMPLE 224: Benzothiazol-6-yl-[6-(l-methanesulfonyl-l,2,3,6- tetrahydropyridin-4-yl)-7iϊ-pyrrolo [2,3-rf] pyrimidin-4-yl] amine.

[628] To a solution of benzothiazol-6-yl-[6-(l ,2,3,6-tetrahydropyridin-4-yl)-7H- pyrrolo[2,3-d]pyrimidin-4-yl]amine trihydrochloride (lOOmg, 0.2mmol) in DMF (5mL) was added N^V-diisopropylethylamine (0.4mL, 2.0mmol) and methanesulfonic anhydride (42mg,

0.24mmol). The reaction mixture was left to stir at rt for Ih. The mixture was concentrated in vacuo and purified via MDP, which afforded the title compound as a tan solid. MS (ES+): m/z: 426.98 (100) [MH⁺]. HPLC: U = 2.44 min (ZQ2000: polarj min). ¹H ΝMR (400 MHz,

CDCl₃): δ = 2.64 (m, 2H), 3.13-3.20 (m, 3H), 3.91 (s, 2H), 6.47 (s, IH), 6.87 (s, IH), 7.87

(dd, J= 1.6, 8.8 Hz, IH), 8.02 (d, J= 8.8 Hz, IH), 8.35 (s, IH), 8.92 (d, J= 2.0 Hz, IH), 9.23

(s, IH), 9.64 (s, IH), 12.04 (s, IH).

[629] General procedure for preparation of a sulfonamide library:

[630] To a solution of benzothiazol-6-yl-[6-(l ,2,3 ,6-tetrahydropyridin-4-yl)-7H- pyrrolo[2,3-c?]pyrimidin-4-yl]-amine tris-hydrochloride (25.3mg, 0.069mmol) in DMF

(0.5mL) at 4°C was added NN-diisopropylethylamine (40mg, 5eq.) followed by the corresponding sulfonyl chloride (leq.). The resulting mixture was allowed to warming up to rt and stirred for 3h. The products were purified by preparative ΗPLC with water / acetonitrile /formic acid mixtures and are assumed to be formate salts.

[631] EXAMPLE 225: Benzothiazol-6-yl-[6-(l-ethanesuIfonyI-l,2,3,6-tetra- hydropyridin-4-yl)-7H-pyrroIo[2,3-<flpyrimidin-4-yl]-amine.

[632] Following the general procedure, the title compound was isolated as tan powder. ¹HNMR (400 MHz, DMSOd₆): δ = 11.97 (s, IH), 9.56 (s, IH), 9.17 (s, IH), 8.85 (d, IH, J= 2.1 Hz), 8.28 (s, IH), 7.99 (d, IH, J= 8.9 Hz), 7.80 (dd, IH, J= 2.1 Hz & 8.9 Hz), 6.87 (s, IH), 6.40 (s, IH), 3.91 (br s, 2H), 3.43 (t, 2H, J= 5.7 Hz), 3.07 (q, 2H, J= 4.3 Hz), 2.54 (br s, 2H), 1.19 (t, 3H, J= 5.7 Hz). LC/MS: m/z 440.92 [MH⁺] (100), t_κ = 2.57 min (ZQ2000, polar_5min). [633] EXAMPLE 226: Benzothiazol-6-yl-{6-[l-(propane-l-suIfonyl)-l,2,3,6- tetrahydropyridin-4-yl] -7iϊ-pyr rolo [2,3-d] pyrimidin-4-yl}-amine.

[634] Following the general procedure, the title compound was isolated as tan powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 12.02 (s, IH), 9.56 (s, IH), 9.19 (s, IH), 8.86 (d, IH₅ J= 2.1 Hz), 8.28 (s, IH), 7.99 (d, IH, J= 8.9 Hz), 7.80 (dd, IH, J= 2.1 Hz & 8.9 Hz), 6.79 (s, IH), 6.40 (s, IH), 3.90 (br s, 2H), 3.42 (t, 2H, J= 5.7 Hz), 3.04 (t, 2H, J= 5.7 Hz), 2.53 (br s, 2H), 1.64 (m, 2H), 0.93 (t, 3H, J= 7.4 Hz). LC/MS: m/z 454.96 [MH⁺] (100), t_κ = 2.72 min (ZQ2000, ρolar_5min).

[635] EXAMPLE 227: Benzothiazol-6-yl-{6-[l-(propane-2-sulfonyl)-l ,2,3,6- tetrahydropyridin-4-yl] -IH-pyr rolo [2,3-rf] pyrimidin-4-yl}-amine.

[636] Following the general procedure, the title compound was isolated as tan powder. ¹H NMR (400 MHz, DMSO-d₆): 5 = 11.97 (s, IH), 9.56 (s, IH), 9.18 (s, IH), 8.85 (d, IH, J= 2.1 Hz), 8.29 (s, IH), 7.97 (d, IH, J= 8.9 Hz), 7.81 (dd, IH, J= 2.1 Hz & 8.9 Hz),

6.79 (s, IH), 6.39 (s, IH), 3.95 (br s, 2H), 3.51 (t, 2H, J= 5.5 Hz), 3.38 (m, IH), 2.51 (br s, 2H), 1.18 (d, 6H, J= 6.8 Hz). LC/MS: m/z 454.95 [MH⁺] (100), *_R = 2.68 min (ZQ2000, polar_5min).

[637] EXAMPLE 228: Benzothiazol-6-yl-[6-(l-cyclopropanesuIfonyl-l,2,3,6- tetrahydropyridin-4-yl)-7H-pyr rolo [2,3-rf] pyrimidin-4-yI] -amine.

[638] Following the general procedure, the title compound was isolated as tan powder. ¹HNMR (400 MHz, DMSOd₆): δ = 11.93 (s, IH), 9.56 (s, IH), 9.17 (s, IH), 8.85 (d, IH, J= 2.0 Hz), 8.28 (s, IH), 7.97 (d, IH, J= 8.9 Hz), 7.78 (dd, IH, J= 2.0 Hz & 8.9 Hz),

6.80 (s, IH), 6.41 (s, IH), 3.93 (br s, 2H), 3.41 (t, 2H, J= 5.6 Hz), 2.62 (m, IH), 2.57 (br s, 2H), 0.92 (m, 4H). LC/MS: m/z 452.94 [MH⁺] (100), h = 2.64 min (ZQ2000, polar_5min). [639] EXAMPLE 229: 4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yI]-3,6-dihydro-2H-pyridine-l-sulfonic acid dimethylamide.

[640] Following the general procedure, the title compound was isolated as tan powder. ¹H NMR (400 MHz, DMSOd₆): δ = 11.97 (s, IH), 9.56 (s, IH), 9.17 (s, IH), 8.86

(d, IH, J= 2.1 Hz), 8.27 (s, IH), 7.97 (d, IH, J= 8.9 Hz), 7.78 (dd, IH, J= 2.1 Hz & 8.9 Hz),

6.79 (s, IH), 6.38 (s, IH), 3.87 (br s, 2H), 3.39 (t, 2H, J= 5.7 Hz), 2.78 (s, 6H), 2.52 (br s,

2H). LC/MS: m/z 455.97 [MH⁺] (100), t_κ = 2.66 min (ZQ2000, polar_5min).

[641] EXAMPLE 230: Benzothiazol-6-yl-{6-[l-(butane-2-sulfonyl)-l,2,3,6- tetrahydropyridin-4-yl]-7_JH^r-pyrrolo[2,3-rf]pyrimidin-4-yl}-amine.

[642] Following the general procedure, the title compound was isolated as tan powder. ¹H NMR (400 MHz, DMSOd₆): δ = 11.97 (s, IH), 9.60 (s, IH), 9.18 (s, IH), 8.85 (d, IH, J= 2.1 Hz), 8.27 (s, IH), 7.97 (d, IH, J= 8.9 Hz), 7.81 (dd, IH, J= 2.1 Hz & 8.9 Hz), 6.79 (s, IH), 6.39 (s, IH), 3.95 (br s, 2H), 3.51 (m, 2H), 3.19 (m, IH), 2.53 (br s, 2H), 1.83 (m, IH), 1.39 (m, IH), 1.17 (d, 3H, J= 6.8 Hz), 0.89 (t, 3H, J= 7.5 Hz). LC/MS: m/z 468.98 [MH⁺] (100), t_κ = 2.84 min (ZQ2000, polar_5min).

[643] EXAMPLE 231: [6-(l-Benzenesulfonyl-l,2,3,6-tetrahydropyridin-4-yl)-

7H-pyrrolo[2,3-rf]pyrimidin-4-yl]-benzothiazoI-6-ylamine.

[644] Following the general procedure, the title compound was isolated as tan powder. ¹H NMR (400 MHz, DMSO-d₆): δ = 11.98 (s, IH), 9.54 (s, IH), 9.16 (s, IH), 8.84 (d, IH, J= 2.1 Hz), 8.29 (s, IH), 7.96 (d, IH, J= 8.9 Hz), 7.81 (dd, IH, J= 2.1 Hz & 8.9 Hz), 7.76 (dd, 2H, J= 1.5 Hz & 7.8 Hz), 7.67 (m, IH), 7.59 (dd, J= 7.8 Hz & 7.8 Hz), 6.74 (s, IH), 6.31 (s, IH), 3.68 (br s, 2H), 3.17 (t, 2H, J= 5.7 Hz), 2.54 (br s, 2H). LC/MS: m/z 488.88 [MH⁺] (100), t_κ = 2.97 min (ZQ2000, polar_5min).

[645] EXAMPLE 232: l-4-[4-(lH-Indol-5-yIamino)-7i3-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yl-3-piperidin-l-ylpropan-l-one.

[646] A mixture of l-[4-(4-chloro-7H-pyrrolo[2,3-J]pyrimidin-6-yl)-3,6-dihydro-

2ϋT-pyridin-l-yl]-3-piperidin-l-ylpropan-l-one (67.7mg, 0.114mmol, leq), 5-aminoindole (18.0mg, 0.136mmol, 1.2eq), and TFA (45//L, 0.58mmol, 5eq) in TFE (1.2mL), in a sealed tube, was heated at 10O⁰C for 5d and concentrated under reduced pressure. The crude material was adsorbed onto Hydromatrix, dry loaded, and purified by chromatography on silica gel [Jones Flashmaster, 5g / 25mL cartridge, eluting with MeOH:DCM 5% -» 7N NH₃/Me0H:DCM 2% → 6%]. Fractions containing product were combined, concentrated in vacuo, and purified by HPLC to give the title compound as a yellow solid. ¹H NMR (400 MHz, CDCl₃): S = 1.46 (s, br, 2H), 1.60 (sextet, J= 5.6 Hz, 4H), 2.22 & 2.29 (s, br, rotamers, 2H), 2,44 (s, br, 4H), 2.51-2.61 (m, 2H), 2.63-2.70 (m, 2H), 3.58 & 3.68 (t, J= 5.6 Hz, rotamers, 2H), 4.16 & 4.21 (s, br, rotamers, 2H), 5.50 & 5.51 (s, br, rotamers, IH), 6.05 & 6.10 (s, br, rotamers, IH), 6.54 (t, J= 3.2 Hz, IH), 7.19 & 7.21 (dt, J= 8.4, 2.0 Hz, IH), 7.29 (d, J= 3.2 Hz, IH), 7.43 (d, J= 8.4 Hz, IH), 7.67 (d, J= 2.0 Hz, IH), 8.21 (s, IH). MS (ES+): m/z 373.05 (100) [MH⁺]. HPLC: fe = 1.72 min (ZQ2000, polar_5min). [647] l-[4-(4-Chloro-7H-pyrrolo[2,3-rf]pyrimidin-6-yl)-3,6-dihydro-2H- pyridin-l-yl]-3-piperidin-l-ylpropan-l-one

[648] To a suspension/solution of 4-chloro-6-(l ,2,3,6-tetrahydropyridin-4-yl)-7H- pyrrolo[2,3-tf]pyrimidine tø-hydrochloride (19.1mg, 0.0621mmol, leq), 1- piperidinepropanoic acid (24.5mg, 0.156mmol, 2.5eq), 1-hydroxybenzotriazole (HOBt) (8.5mg, 0.063mmol, leq), andN-(3-dimethylaminopropyl)-N-ethylcarbodiimide hydrochloride (EDC) (36.3mg, 0.189mmol, 3eq) in anhydrous DMF (1.3mL), DiPEA (64μL, 0.37mmol, 6eq) was added and the reaction was stirred at rt, under N₂, for 16h. Solvent was concentrated in vacuo and the residue was dissolved in DCM, washed with NaHCO₃ (2x) and brine (Ix), dried over anhydrous Na₂SO₄, filtered, and concentrated under reduced pressure. The crude material was purified on MDPS giving the title compound as a yellow solid. ¹H NMR (400 MHz, MeOHM,): δ = 1.45-1.56 (s, br, 2H), 1.64 (sextet, J= 5.6 Hz, 4H), 2.46- 2.78 (m, 10H), 3.81 & 3.84 (t, J= 5.6 Hz, rotamers, 2H), 4.29 & 4.33 (d, J= 2.0 Hz, rotamers, 2H), 6.48 (s, br, IH), 6.62 & 6.63 (s, rotamers, IH), 8.50 (d, IH). MS (ES+): m/z 373.99/376.00 (100/36) [MH⁺]. HPLC: t_R = 1.86 min (ZQ2000, polar_5min). [649] Alternative preparation: To a suspension/solution of 4-chloro-6-(l, 2,3,6- tetrahydropyridin^-yl)-7H-pyπ:olo[2,3-d]pyrimidine δw-hydrochloride (495.4mg, 1.610mmol, leq), 1-piperidinepropanoic acid (335.4mg, 2.133mmol, 1.3eq), and TBTU (624.4mg, 1.945mmol, 1.2eq) in anhydrous DMF (15mL), DiPEA (1.4mL, 8mmol, 5eq) was added at rt, under N₂, and stirred for 2h. The solvent was evaporated under reduced pressure. The crude material was adsorbed onto Hydromatrix, dry loaded, and purified by chromatography on silica gel [Jones Flashmaster, 5Og / 15OmL cartridge, eluting with MeOH:DCM 2% → 5% → 10% → 7N NH₃/Me0H:DCM 2% → 5%]. Fractions containing product were combined and concentrated in vacuo, affording the title compound as a yellow solid.

[650] 4-Chloro-6-(l,2,3,6-tetrahydropyridin-4-yl)-7_JH-pyrrolo[2,3-rf]pyrimidine

6is-hydrochloride

[651] To 4-(4-chloro-7H-pyrrolo[2,3-<|pyrimidin-6-yl)-3,6-dihydro-2H-pyridine-l- carboxylic acid tert-butyl ester (601.6mg, 1.797mmol, leq), a 4.0 M solution of HCl in 1,4- dioxane (15mL, 33eq) was added and the reaction was stirred at rt for 18h. The solid was then filtered off, washed several times with ether, and dried under vacuum pressure, yielding the title compound as a yellow solid. ¹H NMR (400 MHz, DMSO-J₁₅): δ = 2.77 (s, 2H), 3.33 (d, J= 4.8 Hz, 2H), 3.83 (s, br, 2H), 5.27-5.65 (s, br, -NH + H₂O), 6.60 (s, IH), 6.71 (d, J= 1.6 Hz, IH), 8.59 (s, IH), 9.30 (s, br, -NH), 12.85 (s, H⁺). MS (ES+): m/z 235.09/237.11 (3) [MH⁺]; 206.12/208.14 (100) [MH⁺-CH₃N). HPLC: t_κ = 1.52 min (ZQ2000, polar_5min). [652] EXAMPLE 233: l-4-[4-(Benzotriazol-l-yloxy)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2fi-pyridin-l-yl-3-piperidin-l-ylpropan-l-one.

[653] The title compound was also isolated from the TBTU-coupling reaction mixture from the preparation of l-[4-(4-chloro-7/f-pyrrolo[2,3-cT|pyrimidin-6-yl)-3,6- dihydro-2H-pyridin-l-yl]-3-piperidin-l-yl-propan-l-one, after concentration in vacuo at «50°C bath temp., and purified by HPLC, yielding a yellow solid. ¹H NMR (400 MHz, CDCl₃): δ = 1.45 (s, br, 2H), 1.61 (pentet, J= 5.6 Hz, 4H), 2.50 (s, br, 4H), 2.55-2.73 (m, 4H), 2.74-2.84 (m, 2H), 3.73 & 3.84 (t, J= 5.6 Hz, rotamers, 2H), 4.20 & 4.30 (s, br, rotamers, 2H), 6.34 & 6.41 (s, br, rotamers, IH), 6.49 & 6.54 (s, rotamers, IH), 7.44-7.51 (m, 2H), 7.52-7.58 (m, IH), 8.15 (ά, J= 8.4 Hz, IH), 8.27 (s, IH). MS (ES+): m/z 473.03 (100)

[MH⁺]. HPLC: /_R = 2.08 min (ZQ2000, polar_5min).

[654] EXAMPLE 234: 4-[4-([l,2,3]Triazolo[4,5-6]pyridin-3-yloxy)-7H- pyrrolo [2,3-d\ pyrimidin-6-yl] -3 ,6-dihydro-2fl-pyridine-l-carboxylic acid tert-butyl ester.

[655] A solution of 4-(4-chloro-7H-pyrrolo[2,3-J]pyrimidin-6-yl)-3,6-dihydro-2H- pyridine-1-carboxylic acid tert-butyl ester (11.5mg, 0.0343mmol, leq) and l-hydroxy-7- azabenzotriazole (HO At) (5.6mg, 0.041mmol, 1.2eq) in H-butanol (ImL) was stirred at 80 °C for 15h. Solid that had formed during the course of the reaction was filtered over a Hirsh funnel and washed with minimal n-butanol. The filtrate was concentrated in vacuo. To a solution of the solid (3-[6-(l,2,3,6-tetrahydropyridin-4-yl)-7H-pyrrolo[2,3-rf]pyrimidin-4- yloxy]-3H-[l,2,3]triazolo[4,5-δ]pyridine) (6.4mg, 0.015mmol, leq) in DMSO (ImL), di-tert- butyldicarbonate (5.0mg, 0.023mmol, 1.5eq) and DiPEA (20 μL, O.lmmol, 7eq) were added and the reaction was stirred at rt for 2h. This solution was combined with the concentrated filtrate and purified on the MDPS yielding the title compound. ¹H NMR (400 MHz, MeOH- d₄): δ = 1.51 (s, 9H), 2.64 (s, br, 2H), 3.70 (s, br, 2H), 4.17 (s, br, 2H), 6.46 (s, br, IH), 6.74 (s, IH), 7.61 (dd, J= 8.4, 4.4 Hz, IH), 8.13 (s, IH), 8.61 (d, J= 8.0 Hz, IH), 8.74 (d, J= 4.4 Hz, IH). MS (ES+): m/z 435.00 (62) [MH⁺]. HPLC: Z_R = 3.36 min (ZQ2000, polar_5min). [656] 3-[6-(l,2,3,6-Tetrahydropyridin-4-yl)-7H-pyrroIo[2,3-^pyrimidin-4- yloxy] -3H-[1 ,2,3] triazolo [4,5-Z>] pyridine

[657] ¹H NMR (400 MHz, DMSO-^): δ = 2.81 (s, br, 2H), 3.35-3.45 (m, 2H +

H₂O), 3.85 (s, br, 2H), 6.63 (s, IH), 6.96 (d, J= 1.6 Hz, IH), 7.67 (dd, J= 8.0, 8.4 Hz, IH), 8.26 (s, IH), 8.75-8.82 (m, 2H), 9.41 (s, br, -NH)₁ 13.01 (s, -NH). MS (ES+): m/z 335.04 (2) [MH⁺]. HPLC: k = 1.73 min (ZQ2000, polar5min).

[658] General procedure for coupling of aminopyridines with 4-(4-chloro-7H- pyrrolo[2,3-d]pyrimidin-6-yl)-3,6-dihydro~2H-pyridine-l-carboxylic acid tert-butyl ester (EXAMPLES 235-237): [659] To a mixture of 4-(4-chloro-7H-pyrrolo[2,3-£Tlpyrimi(lin-6-yl)-3,6-dihydro-

2#-pyridine-l-carboxylic acid tert-hutyl ester (134mg, 0.4mmol), substituted-4- aminopyridine (0.6mmol), (R)-(+)-2,2'-bis(diphenylphosphino)4,r-binaphthyl (75mg, 0.04mmol) and sodium *-butoxide (77mg, 0.8mmol) was added degassed DMF (3mL), and the reaction was heated overnight at 70°C under N₂. The reaction was cooled to RT, filtered and purified through mass directed HPLC purification system. The product obtained was further purified by preparative TLC using DCM:methanol mixture as eluent to afford pure product.

[660] EXAMPLE 235: 4-{4-[2-(4-MethyIpiperazin-l-yI)-pyridin-4-ylamino]-

7H-pyrroIo[2,3-rf]pyrimidin-6-yI}-3,6-dihydro-2J3-pyridine-l-carboxyIic acid tert-butyl ester.

[661] Following the general procedure described above, and employing 2-(4- methylpiperazin-l-yl)-pyridin-4-ylamine, the reaction afforded 4-{4-[2-(4-methylpiperazin-l- yl)-pyridin-4-ylamino]-7H-pyrrolo[2,3-^pyrimidin-6-yl}-3,6-dihydro-2H-pyridine-l- carboxylic acid tert-butyl ester. ¹HNMR (400 MHz, CD₃OD): δ = 8.21-8.26 (m, IH), 7.82- 7.86 (m, IH), 7.46 (d, J= 7.1 Hz, IH), 7.09-7.11 (m, IH), 6.64 (s, IH), 6.38-6.43 (m, IH), 6.19 (bs, IH), 4.01 (bs, IH), 3.52-3.57 (m, 2H), 3.40-3.44 (m, 4H), 3.17-3.20 (m, IH), 2.46- 2.51 (m, 6H), 2.26 (s, 3H), 1.39 (s, 9H); MS (ES+): m/z 491.11 (100) [MH⁺]; HPLC: t_R = 1.90 min (ZQ2000, polar__5min). [662] 2-(4-Methylpiperazin-l-yl)-pyridin-4-ylamine

[663] To a mixture of 1 -methyl-4-(4-nitropyridin-2-yl)-piperidine (450mg,

2.024mmol), iron powder (1.130g, 20.2mmol), ethanol (8mL) and water (2mL) was added concentrated HCl (0.055mL, O.δmmol) and the mixture was heated to reflux for 3h. The reaction mixture was cooled to RT, filtered, filter cake washed with ethanol and the filtrate was evaporated. To the residue, aqueous saturated sodium bicarbonate solution (5mL) and water (2OmL) were added and extracted with DCM (3x40mL). The DCM extract was washed with brine, dried over anhydrous sodium sulphate and evaporated to afford the title compound as a reddish pink solid. MS (ES+): m/z 193.27 (100) [MH⁺]; HPLC: t_κ = 0.32 min (ZQ2000, polar_5min). [664] l-Methyl-4-(4-nitropyridin-2-yl)-piperazine

[665] To a solution of 2-chloro-4-nitropyridine (793mg, 5mmol) in pyridine

(1OmL) was added 1-methylpipeazine (0.555mL, 5mmol) and the mixture was heated to 9O⁰C overnight. The reaction mixture was evaporated under reduced pressure, water was added to the residue followed by saturated aqueous sodium bicarbonate (3mL) and extracted with DCM (4x50mL). The combined DCM layer was washed with brine, dried over anhydrous sodium sulfate and evaporated under reduced pressure. The crude product was purified by chromatography on silica gel [Jones Flashmaster, 7Og / 15OmL cartridge, eluting with DCM:Methanol 100:0 — > 98:2], yielding the title compound as orange-yellow solid (311mg, 28 % ). ¹H NMR (400 MHz, CDCl₃): δ = 8.36 (dd, J= 5.3, 0.36 Hz, IH), 7.32 (d, J= 1.6 Hz, IH), 7.24 (dd, J= 5.4, 1.8 Hz, IH), 3.67 (t, J= 5.3 Hz, 4H), 2.53 (t, J= 5.2 Hz, 4H), 2.36 (s, 3H); MS (ES+): m/z 223.21 (100) [MH⁺]; HPLC: ^ = 0.49 & 1.37 min (ZQ2000, polar_5min).

[666] EXAMPLE 236: 4-{4-[2-Chloro-6-(4-methyIpiperazin-l-yl)-pyridin-4- ylaraino] ~7H-pyrroIo [2,3-d] pyrimidin-6-yI}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester.

[667] Following the general procedure described above, and employing 2-chloro-6-

(4-methylpiperazin-l-yl)-pyridin-4-ylamine, the reaction afforded the title compound. ¹H NMR (400 MHz, CD₃OD): δ = 8.23-8.27 (m, IH), 7.21-7.24 (m, 2H), 6.87 (s, IH), 6.42 (s, IH), 6.20 (bs, IH), 4.02 (bs, IH), 3.50-3.60 (m, 2H), 3.41-3.47 (m, 4H), 3.19-3.21 (m, IH), 2.42-2.47 (m, 6H), 2.25 (s, 3H), 1.40 (s, 9H); MS (ES+): m/z 525.04 (100) [MH⁺]; HPLC: t_κ ~ 2.31 min (ZQ2000, polar_5min).

[668] 2-Chloro-6-(4-methylpiperazin-l-yl)-pyridin-4-ylamine & 2,6-Bis-(4- methylpiperazin-l-yl)-pyridin-4-ylamine

[669] A mixture of 4-amino-2,6-dichloropyridine (1.0Og, 6.14mmol) and 1-methyl- piperazine (0.68mL, 6.1mmol) in pyridine (10 mL) was heated at 150⁰C for 3d under N₂. The reaction mixture was evaporated under reduced pressure, and to the residue water was added followed by saturated aqueous sodium bicarbonate (5mL) and extracted with DCM (4x50mL). The combined DCM layer was washed with brine, dried over anhydrous sodium sulfate and evaporated under reduced pressure. The crude product was purified by chromatography on silica gel [Jones Flashmaster, 7Og / 15OmL cartridge, eluting with DCM:2N NH₃ in methanol [100:0 → 75:25], yielding the title compounds. 2-Chloro-6-(4- methylpiperazin-l-yl)-pyridin-4-ylamine: MS (ES+): m/z 227.18 (100) [MH⁺]; HPLC: t_R = 0.48 & 1.07 min (ZQ2000, polar_5min). 2,6-Bis-(4-methylpiperazin-l-yl)-pyridin-4- ylamine: MS (ES+): m/z 291.21 (100) [MH⁺]; HPLC: t_κ = 0.31 min (ZQ2000, polar_5min). [670] EXAMPLE 237: 4-{4-[2,6-£/s-(4-methyIpiperazin-l-yl)-pyridin-4- ylamino] -lH-γ>y rrolo [2,3-rf] py rimidin-6-yl}-3 ,6-dihy dro-2iϊ-pyridine-l -carboxylic acid tert-butyl ester.

[671] Following the general procedure described above, and employing 2,6-bis-(4- methylpiperazin-l-yl)-pyridin-4-ylamine, the reaction afforded the title compound. ¹H NMR (400 MHz, CD₃OD+CDCI₃): δ = 8.27-8.31 (m, IH), 6.48-6.55 (m, 3H), 6.19 (bs, IH), 4.09 (bs, 2H), 3.60 (t, J= 5.6 Hz, 2H), 3.47-3.51 (m, 8H), 2.50-2.54 (m, 10H), 2.30 (s, 6H), 1.45 (s, 9H); MS (ES+): m/z 589.13 (100) [MH⁺]; HPLC: t_R = 1.84 min (ZQ2000, polar_5min). [672] EXAMPLE 238: 4-[4-(6-CarbamoyIpyridin-3-ylamino)-7H-pyrrolo[2,3- rf]pyrimidin-6~yl]-3,6-dihydro-2iϊ-pyridme-l-carboxylic acid tert-butyl ester.

[673] Into the DMF (ImL) solution of 4-(4-chloro-7H-pyrrolo[2,3-J]pyrimidin-6- yl)-3,6-dihydro-2H-pyridine-l-carboxylic acid fert-butyl ester (122mg, 0.363mmol) was added /-BuOK (IM in J-BuOH, 0.726mL, 0.726mmol) dropwise at RT under N₂ over 5min. The mixture was then put in an ice/water bath and stirred for lOmin. After that time, the DMF (ImL) solution of 5-aminopyridine-2-carboxylic acid amide (99.5mg, 0.726mmol) was added into the above mixture dropwise. The reaction mixture was warmed to RT. Pd₂(dba)₃-CΗC1₃ (9.4mg, 2.5%eq.) and R(+)-BINAP (22.6mg, O.leq.) were added, and the mixture was heated at 100⁰C for 24h. The mixture was filtered and the filtrate was concentrated in vacuo. The crude was submitted to MS directed purification. A brown oil was obtained that was purified further by HPLC to obtain the title compound as an off-white solid. ¹H NMR (DMSO-d«, 400 MHz): δ = 1.50 (s, 9 H), 2.50 (m, 2 H), 3.64 (t, 2 H, J= 5.6 Hz), 4.12 (bra, 2 H), 6.50 (bra, 1 H), 6.88 (s, 1 H), 7.53 (d, 1 H, J= 4.2 Hz), 8.04 - 8.05 (m, 1 H), 8.08 (d, 1 H, J= 8.8 Hz), 8.44 (s, 1 H), 8.68 (dd, 1 H, J= 2.4 & 8.4 Hz), 9.12 (d, 1 H, J= 2.4 Hz), 9.91 (s, 1 H), 12.18 (s, 1 H). MS (ES+): m/z 436.10 (100) [MH⁺]. HPLC: *_R = 2.75 min (ZQ2000, polar_5 min).

[674] S-Aminopyridine-l-carboxylic acid amide o

^-N NH₂

[675] MeOH (3OmL) was added into the mixture of 5-aminopyridine-2-carbonitrile

(1191mg, lO.OOmmol), NaBO₃-H₂O (2995mg, 30.00mmol), and H₂O (3OmL), and the mixture was then heated at 5O⁰C for 16h. The mixture was then concentrated in vacuo, then treated with water (3OmL), and extracted with EtOAc (4 x 5OmL). The combined extracts were dried over MgSO₄, filtered, and concentrated in vacuo to obtain a yellow solid. The solid was triturated with 4OmL of 40% EtOAc/hexane to yield the title compound as yellow solid. ¹H NMR (DMSO-J₁₅, 400 MHz): δ = 5.86 (s, 2 H), 6.89 (dd, 1 H, J= 2.4 & 8.4 Hz), 7.07 (brs, 1 H), 7.59 (brs, 1 H), 7.64 (d, 1 H, J= 8.4 Hz), 7.83 (d, 1 H, J= 2.4 Hz). MS (ES+): m/z 138.18 (100) [MH⁺]. HPLC: t_κ = 0.75 min (ZQ2000, polar_5 min). [676] EXAMPLE 239: 4-[4-(6-Methoxypyridin-3-ylamino)-7H-pyrrolo[2,3- rf]pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid fer/-butyl ester.

[677] The title compound was obtained following the procedure for the synthesis of

4-[4-(6-carbamoylpyridin-3-ylamino)-7H-pyrrolo[2,3-£T|pyrimidin-6-yl]-3,6-dihydro-2H- pyridine- 1-carboxylic acid fert-butyl ester, but using 6-methoxypyridin-3-ylamine in place of 5-aminopyridine-2-carboxylic acid amide. ¹H NMR (CD₃OD, 400 MHz): δ = 1.40 (s, 9 H), 2.47 (m, 2 H), 3.57 (m, 2 H), 4.00 (m, 2 H), 6.19 (brs, 1 H), 6.50 (s, 1 H), 6.74 (s, 1 H, d, 1 H, J= 9.2 Hz), 7.48 (dd, 1 H, J= 2.8 Hz & 8.8 Hz), 8.04 - 8.05 (m, 1 H), 8.07 (s, 1 H), 8.31 (d, 1 H, J= 3.2 Hz). MS (ES+): m/z 423.08 (100) [MH⁺]. HPLC: t_R = 2.86 min (ZQ2000, polar_5 min). [678] EXAMPLE 240: 4-[4-(6-Oxo-l,6-dihydropyridin-3-ylamino)-7#- pyrrolo[2,3-<flpyrimidin-6-yl]-3,6-dihydro-2/?-pyridine-l-carboxylic acid tert-butyl ester.

[679] Into the suspension of 4-[4-(6-methoxypyridin-3-ylamino)-7H-pyrrolo[2,3- rf]pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester (68.4mg, 79% purity, 0.127mmol) and NaI (19.1mg, 0.127mmol) in CH₃CN (1OmL) was added trimethylsilyl chloride (1 M in THF, 0.765mL, 0.765mmol) at rt. The mixture was then heated at 8O⁰C in a flask under N₂ for 48h. After that time, the mixture was cooled at 0⁰C and the aqueous solution (H₂O, 8mL) OfNaHCO₃ (159mg) and NaS₂O₄- 5H₂O (318mg) was added while stirring. The solid was filtered off and washed with water to obtain a brown-red solid. Boc₂O (30.8mg, 0.140mmol), DMAP (17.1mg, 0.140mmol) and the above solid were dissolved in pyridine and the mixture was stirred at rt for 18h. After that time, the mixture was concentrated in vacuo to obtain a green-yellow oil that was submitted for MS directed purification. One obtained the title compound as off-white solid. ¹H NMR (DMSO-J₀, 400 MHz): δ = 1.44 (s, 9 H), 2.46 (bra, 2 H), 3.56 (t, 2 H, J= 5.4 Hz), 4.00 (bis, 2 H), 6.38 (s, 1 H), 6.40 (s, 1 H), 6.67 - 7.70 (m, 1 H), 8.02 (d, 1 H, J= 2.4 Hz), 8.20 (s, 1 H), 9.06 (s, 1 H), 11.40 (brs, 1 H), 11.92 (s 1 H). MS (ES+): m/z 409.05 (100) [MH⁺]. HPLC: t_κ = 2.33 min (ZQ2000, polar_5 min).

[680] EXAMPLE 241: 4-[4-(l-Methyl-6-oxo-l,6-dihydropyridin-3-ylamino)-

7H-pyrrolo[2,3-^pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester.

[681] The title compound was obtained following the General method for the reaction of amines with teii-butyl 4-(4-chloro-7H-pyrrolo[2,3-d]pyrimidin-6-yl)-3,6- dihydropyridine-l(2H)-carboxylate, using 5-amino-l-methyl-lH-pyridin-2-one. ¹H NMR (DMSO-tfβ, 400 MHz): δ = 1.44 (s, 9 H), 2.43 (brs, 2 H), 3.46 (s, 3 H), 3.56 (t, 2 H, J= 6.4 Hz), 4.04 (brs, 2 H), 6.38 (brs, 1 H), 6.43 (d, 1 H, J= 9.6 Hz), 6.61 (s, 1 H), 7.63 (dd, 1 H, J= 2.8 & 9.6 Hz), 8.18 - 8.20 (m, 2 H), 9.07 (s, 1 H), 11.91 (s, 1 H). MS (ES+): m/z 423.07 (100) [MH⁺]. HPLC: t_R = 2.38 min (ZQ2000, polar_5 min). [682] 5-Amino-l-methyI-ljff-pyridin-2-one

[683] To a suspension of 5-nitro-l-methyl-2(lH)-pyridone (154mg, 0.999mmol) in ethyl acetate (3mL) and ethanol (3mL) was added 5% Pd-C (36mg), and the resulting mixture was stirred under hydrogen atmosphere overnight. The reaction mixture was filtered and the filtrate was concentrated in vacuo to obtain the title compound as light-green oil. ¹H NMR (CD₃OD 400 MHz): δ = 3.53 (s, 3 H), 6.49 (d, 1 H, J= 9.6 Hz), 7.07 (d, 1 H, J= 3.2 Hz), 7.28 (dd, 1 H, J= 2.8 & 9.6 Hz). MS (ES+): m/z 125.04 (100) [MH⁺]. HPLC: fe = 0.43 min (ZQ2000, polar_5 min). [684] l-Methyl-5-nitro-lH-pyridin-2-one

[685] Tetra-N-butylammonium bromide (3220mg, lO.OOmmol), sodium hydroxide

(400.0mg, lO.OOmmol) and methyl iodide (3113μL, 50.00mmol) were sequentially added into the two-phase mixture of 2-hydroxy-5-nitropyridine (700.0mg, 5.000mmol) in water (25mL) and methylene chloride (5OmL). The above mixture was stirred at rt for Ih and then partitioned between CH₂Cl₂ (5OmL) and water (75mL). The aqueous layer was extracted with CH₂Cl₂ (5OmL). The combined organic phases were dried over MgSO₄, filtered, and concentrated in vacuo to obtain a beige solid. Silica gel (134 g) was used to purify the above solid eluting with 250OmL EtOAc to obtain the title compound as beige powder. ¹H ΝMR (CDCl₃, 400 MHz): δ = 3.66 (s, 3 H), 6.57 (d, I H, /= 10.0 Hz), 8.10 (dd, 1 H, J= 2.8 & 10.0 Hz), 8.63 (d, 1 H, J= 2.8 Hz). MS (ES+): m/z 155.15 (100) [MH⁺]. HPLC: t_κ = 1.69 min (ZQ2000, polar_5 min).

[686] EXAMPLE 242: 4-[4-(l-Methyl-6-oxo-l,6-dihydropyridin-3-ylamino)-

7H-pyrrolo [2,3-rf] pyrimidin-6-yl] -3,6-dihydro-2H-pyridine-l-carboxylic acid tert- butylamide.

[687] 4-[4-(l-Methyl-6-oxo-l,6-dihydropyridin-3-ylamino)-7H-pyrrolo[2,3- d]pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester (38.0mg, 0.0845mmol), 9M of Hydrogen chloride in Methanol (2mL) and Methanol (2mL) were combined , and the above miture was stirred at rt for 3h. The reaction mixture was concentrated in vacuo to obtain a black solid. DMF (3mL), NEt₃ (58.9μL, 0.423mmol) and tert-butyl isocyanate (14.5μL, 0.127 mol) were added, and the mixture was stirred at rt under N₂ for 1.5h. Another portion of tert-butyl isocyanate was added and the reaction was stirred overnight. The mixture was concentrated in vacuo, and the residue was purified by HPLC to obtain the title compound as pink solid. ¹H NMR (CD₃OD₅400 MHz): δ = 1.36 (s, 9 H), 2.56 (bra, 2 H), 3.61 (m, 2 H), 3.62 (s, 3 H), 4.07 (bra, 2 H), 6.29 (bra, 1 H), 6.58 (s, 1 H), 6.60 (d, 1 H, J= 9.6 Hz), 7.71 (dd, 1 H, J= 2.8 & 9.6 Hz), 8.16 (bra, 2 H), 8.19 (s, 1 H), 8.25 (d, 1 H, J= 2.4 Hz). MS (ES+): m/z 422.12 (100) [MH⁺]. HPLC: t_R = 2.11 min (ZQ2000, polar_5 min).

[688] EXAMPLE 243: 4-[4-(4-Carbamoylphenylamino)-7H-pyrrolo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester.

[689] The title compound was obtained following the General method for the reaction of amines with tert-butyl 4-(4-chloro-7H-pyrrolo[2,3-cT]pyrimidin-6-yl)-3,6- dihydropyridine-1 (2H)-carboxylate, using 4-aniinobenzamide. ¹H NMR (DMSO-J₁₅, 400 MHz): δ = 1.44 (s, 9 H), 2.50 (m, 2 H), 3.58 (t, 2 H₅ J= 5.2 Hz), 4.05 (bra, 2 H)₅ 6.43 (brs, 1 H), 6.84 (s, 1 H)₅ 7.21 (brs, 1 H), 7.86 (m, 3 H)₅ 8.00 (d, 1 H₅ J= 8.4 Hz), 8.34 (s, 1 H), 9.57 (s, 1 H), 12.04 (s, 1 H). MS (ES+): m/z 435.09 (100) [MH⁺]. HPLC: t_R = 2.61 min (ZQ2000, polar_5 min).

[690] EXAMPLE 244: 4-[4-(l-Oxo-2,3-dihydro-lH-isomdol-5-yIamino)-7H- pyrrolo[2,3-rf]pyrimidin-6-yl]-3,6-dihydro-2jH-pyridine-l-carboxylic acid tert-butyl ester.

[691] The title compound was obtained following the General method for the reaction of amines with tert-butyl 4-(4-chloro-7H-pyrrolo[2,3-d]pyrimidin-6-yl)-3₅6- dihydropyridine-l(2H)-carboxylate₅ using 5-amino-2,3-dihydroisoindol-l-one. ¹H NMR (DMSO-4, 400 MHz): δ 1.47 (s, 9 H), 2.50 (m, 2 H)₅ 3.61 (t, 2 H, J= 5.6 Hz), 4.08 (brs, 2 H)₅4.42 (s, 2 H), 6.46 (brs, 1 H)₅ 6.89 (s, 1 H)₅ 7.65 (d, 1 H, J= 8.4 Hz), 7.90 (dd, 1 H₅ J= 0.8 & 8.4 Hz)₅ 8.37 - 8.40 (m, 3 H)₅ 9.67 (s, 1 H), 12.08 (s, 1 H). MS (ES+): m/z 447.10 (100) [MH⁺]. HPLC: t_R = 2.61 min (ZQ2000, polar_5 min). [692] 5-Amino-2,3-dihydroisoindol-l-one

[693] Iron powder (158mg, 2.83mmol), water (61μL), and HCl (37%, 5μL,

0.566mmol) were added into the suspension of 5-nitro-2,3-dihydroisoindol-l-one (50.4mg, 0.283mmol) in EtOH (754μL). The above mixture was heated at 95⁰C for 2h. After that time, several drops of 7N NH₃ in MeOH were added to basify the solution, and the solid was filtered off. The filtrate was concentrated in vacuo to obtain a light-yellow solid that was purified by preparative TLC eluting with 10% MeOH/CH₂Cl₂ to give a light-yellow solid of 5-amino-2,3-dihydroisoindol-l-one. ¹HNMR (CD₃OD, 400 MHz): δ = 7.48 (s, 1 H), 8.08 (s, 2 H), 9.91 (s, 1 H), 10.66 (d, 1 H, J= 8.8 Hz). MS (ES+): m/z 149.21 (100) [MH⁺]. HPLC: t_κ = 1.20 min (ZQ2000, polar_5 min). [694] 5-Nitro-2,3-dihydroisoindol-l-one

[695] AIBN (58.6mg, 0.357mmol), NBS (785mg, 4.46mmol), and 2-methyl-4- nitrobenzoic acid methyl ester (696mg, 3.57mmol) were suspended in CCl₄ (35mL) in a sealed tube. The above mixture was flushed with N₂ for 5min and heated at 8O⁰C for 22h. After cooling, the solid was filtered off and the filtrate was concentrated to dryness to obtain a crude light-brown solid. To above solid was added NH₃ (7 N in MeOH, 5mL), and the mixture was stirred at rt for 2h and concentrated in vacuo to obtain a yellow solid. This crude solid was triturated with EtOAc (15mL) and was then cooled at -20 ⁰C. The mixture was filtered to obtain the title compound as yellow solid. ¹H NMR (DMSO-^, 400 MHz): δ = 4.51 (s, 2 H), 7.13 (bra, 2 H), 7.91 (d, 1 H, J= 8.4 Hz), 8.25 (dd, 1 H, J= 2.0 & 8.4 Hz), 8.48 (d, 1 H, J= 2.0 Hz), 9.04 (brs, 1 H). MS (ES+): m/z 179.22 (100) [MH⁺]. HPLC: t_R = 2.14 min (ZQ2000, polar_5 min). [696] 2-Methyl-4-nitrobenzoic acid methyl ester

[697] H₂SO₄ (98%, 0.03OmL) was added dropwise into the MeOH (3OmL) solution of 2-metliyl-4-nitrobenzoic acid at rt. The mixture was then heated at 55⁰C. After 5Oh, the solvent was removed in vacuo and the residue was partitioned between EtOAc and H₂O (25mL each). The aqueous layer was extracted with another portion of EtOAc (25mL). The combined extracts were washed with saturated NaHCO₃ (25mL), H₂O (2 x 25mL), and brine (25mL), dried over MgSO₄, filtered and concentrated in vacuo to give the title compound as light-yellow solid. ¹H NMR (CDCl₃, 400 MHz): δ = 2.69 (s, 3 H), 3.95 (s, 3 H), 8.03 - 8.12 (m, 3 H). MS (ES+): m/z 196.25 (100) [MH⁺]. HPLC: t_R= 3.29 min (ZQ2000, polar_5 min). [698] EXAMPLE 245: 4-[4-(4-BenzyIoxy-3-chIorophenylammo)-7H- pyrroIo^S-^pyrimidin-ό-yy-Sjό-dihydro^H-pyridine-l-carboxylic acid tert-buty\ ester.

[699] The title compound was obtained following the General method for the reaction of amines with fer/-butyl 4-(4-chloro-7H-pyrrolo[2,3-</|pyrimidin-6-yl)-3,6- dihydropyridine-1 (2H)-carboxylate, using 4-benzyloxy-3 -chlorophenylamine. ¹H NMR (DMSO-J,;, 400 MHz): δ = 1.44 (s, 9 H), 2.52 (brs, 2 H), 3.57 (t, 2 H, J= 5.6 Hz), 4.05 (brs, 2 H), 5.19 (s, 2 H), 6.40 (brs, 1 H), 6.74 (s, 1 H), 7.23 (d, 1 H, J= 9.2 Hz), 7.33 - 7.37 (m, 1 H), 7.40 - 7.44 (m, 2 H), 7.48 - 7.50 (m, 2 H), 7.68 - 7.72 (m, 1 H), 8.13 - 8.15 (m, 1 H), 8.27 (d, 1 H₅ J= 1.2 Hz), 9.34 (s, 1 H), 11.96 (s, 1 H). MS (ES+): m/z 532.02/533.98 (100/38) [MH⁺]. HPLC: h = 3.81 min (ZQ2000, polar_5 min).

[700] EXAMPLE 246: 4-[4-(2-Ammobenzothiazol-6-ylamino)-7H-pyrrolo[2,3-

^pyrimidin-6-yI]-3,6-dihydro-2i?-pyridine-l-carboxyIic acid ferf-butyl ester.

[701] The title compound was obtained following the General method for the reaction of amines with te/Y-butyl 4-(4-chloro-7H-pyrrolo[2,3-<f|pyrimidin-6-yl)-3,6- dihydropyridine-1 (2H)-carboxylate, using benzothiazole-2,6-diamine. ¹H NMR (DMSO-Gk, 400 MHz): δ = 1.40 (s, 9 H), 2.50 (brs, 2 H), 3.52 (brs, 2 H), 4.00 (brs, 2 H), 6.29 (brs, 1 H), 6.65 (brs, 1 H), 7.21 - 7.46 (m, 4 H), 8.21 - 8.28 (m, 2 H), 9.27 (brs, 1 H), 11.88 (brs, 1 H). MS (ES+): m/z 464.03 (50) [MH⁺]. HPLC: t_R = 2.34 min (ZQ2000, polar_5 min). [702] EXAMPLE 247: 4-[4-(2-Amino-l_JH-benzimidazoI-5-ylamino)-7H- pyrroIo[2,3-rf]pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxyIic acid tert-butyl ester.

[703] The title compound was obtained following the General method for the reaction of amines with tert-butyl 4-(4-chloro-7H-pyrrolo[2,3-rf]pyrimidin-6-yl)-3,6- dihydropyridine-l(2H)-carboxylate, using benzimidazole-2,5-diamine, except that the heating was conducted at 140⁰C for 24h. ¹H NMR (CD₃OD, 400 MHz): δ = 1.50 (s, 9 H), 2.48 (brs, 2 H), 3.61 (brs, 2 H), 4.11 (brs, 2 H), 6.24 (brs, 1 H), 6.36 (brs, 1 H), 7.12 (dd, 1 H, J= 2.0 & 8.8 Hz), 7.19 (d, 1 H, J= 8.0 Hz), 7.48 (s, 1 H), 8.12 (s, 1 H). MS (ES+): m/z 447.03 (60) [MH⁺]. HPLC: t_R = 1.97 min (ZQ2000, polar_5 min).

[704] EXAMPLE 248: 4-{4-[3-(2#-[l,2,3]TriazoI-4-yI)-phenylamino]-7iϊ- pyrrolo[2,3-^pyrimidin-6-yI}-3,6-dihydro-2iy-pyridine-l-carboxylic acid tert-butyl ester.

[705] The title compound was obtained following the General method for the reaction of amines with te/t-butyl 4-(4-chloro-7H-pyrrolo[2,3-rf]ρyrimidin-6-yl)-3,6- dihydropyridine-1 (2H)-carboxylate, using 3-(2H-[1 ,2,3]triazol-4-yl)phenylamine. ¹H NMR (DMSO-J₁₅, 400 MHz): δ = 1.40 (s, 9 H), 2.47 (brs, 2 H), 3.54 (t, 2 H, J= 5.2 Hz), 4.01 (brs, 2 H), 6.37 (brs, 1 H), 6.80 (s, 1 H), 7.37 (t, 1 H, J= 8.0 Hz), 7.43 (d, 1 H, J= 8.0 Hz), 7.98 (d, 1 H, J= 8.4 Hz), 8.19 (s, 1 H), 8.26 - 8.31 (m, 2 H), 9.44 (s, 1 H), 11.94 (s, 1 H). MS (ES+): m/z 458.96 (100) [MH⁺]. HPLC: t_R = 2.74 min (ZQ2000, polar_5 min). [706] 3-(2H-[l,2,3]Triazol-4-yl)phenyIamine

[707] The mixture of azidotrimethylsilane (137μL, 1 ,03mmol) and 3-amino- phenylacetylene (117mg, l.OOmmol) was heated in a sealed tube at 15O⁰C for 16h. After that time, the mixture was cooled down and triturated by EtOAc/hexane (50%, 1OmL). The mother liquor was purified by TLC eluting with 7% MeOH/CH₂Cl₂. to give the title compound as brown oil. ¹H NMR (CD₃OD, 400 MHz): δ = 6.61 - 6.64 (m, 1 H), 7.01 - 7.09 (m, 3 H), 7.94 (s, 1 H). MS (ES+): m/z 161.20 (38) [MH⁺]. HPLC: /_R = 1.54 min (ZQ2000, polar_5 min).

[708] EXAMPLE 249: 4-[4-(3-Thiophen-2-yl-phenyIamino)-7H-pyrrolo[2,3- rf]pyrimidin-6-yl]-3,6-dihydro-2iϊ-pyridine-l-carboxylic acid tert-butyl ester.

[709] The title compound was obtained following the General method for the reaction of amines with tert-butyl 4-(4-chloro-7H-pyrrolo[2,3-_</]pyrirmdin-6-yl)-3,6- dihydropyridine-l(2H)-carboxylate, using 3-thiophen-2-ylphenylamine. ¹H NMR (CD₃OD, 400 MHz): δ = 1.52 (s, 9 H), 2.58 (bis, 2 H), 3.68 (bis, 2 H), 4.14 (bis, 2 H), 6.31 (brs, 1 H), 6.69 (s, 1 H), 7.11 - 7.13 (m, 1 H), 7.38 - 7.43 (m, 4 H), 7.68 - 7.71 (m, 1 H), 8.07 (s, 1 H), 8.26 (s, 1 H). MS (ES+): m/z 473.95 (100) [MH⁺]. HPLC: *_R = 3.71 min (ZQ2000, polar_5 min).

[710] EXAMPLE 250: 4-{4-[3-(4-Methylpiperazin-l-yl)-phenyIamino]-7H- pyrrolo [2,3-rf]pyrimidiii-6-yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester.

[711] The title compound was obtained following the General method for the reaction of amines with tert-butyl 4-(4-chloro-7H-pyrrolo[2,3-cf]pyrimidin-6-yl)-3,6- dihydropyridine-1 (2H)-carboxylate, using 3-(4-methylpiperazin-l -yl)-phenylamine. ¹H NMR (CD₃OD, 400 MHz): δ = 1.51 (s, 9 H), 2.56 (brs, 2 H), 2.86 (s, 3 H), 3.31 (brs, 4 H), 3.54 (brs, 4 H), 3.67 (brs, 2 H), 4.14 (brs, 2 H), 6.29 (brs, 1 H), 6.63 (s, 1 H), 6.78 - 6.80 (m, 1 H), 7.20 (d, 1 H, J= 8.0 Hz), 7.26 -7.30 (m, 1 H), 7.53 (s, 1 H), 8.22 (s, 1 H), 8.41 (brs, 2 H). MS (ES+): m/z 490.08 (100) [MH⁺]. HPLC: t_R = 2.15 min (ZQ2000, polar_5 min). [712] 3-(4-Methylpiperazin-l-yI)-phenyIamine

[713] Into the solution of l-methyl-4-(3-nitrophenyl)-piperazine (123mg,

0.556mmol) in ethanol (5mL) was added Pd (10% on carbon, 12.0mg). The mixture was degassed for 5 min and was then was stirred under H₂ atmosphere (balloon pressure) at rt for 24h. After that time, the reaction mixture was filtered and the filtrate was concentrated in vacuo to obtain the title compound as light yellow oil. ¹H NMR (CDCl₃, 400 MHz): δ = 2.35 (s, 3 H), 2.56 (t, 4 H, J= 5.2 Hz), 3.18 (t, 4 H, J= 5.0 Hz), 3.60 (brs, 2 H), 6.21 - 6.23 (m, 1 H), 6.27 (t, 1 H, J= 2.2 Hz), 6.36 - 6.39 (m, 1 H), 7.05 (m, 1 H). MS (ES+): m/z 192.31 (100) [MH⁺]. HPLC: t_R = 0.39 min (ZQ2000, polar_5 min). [714] l-MethyI-4-(3-nitrophenyl)-piperazine

[715] A mixture of 1 -fluoro-3-nitrobenzene (282mg, 2.00mmol), 1 -methyl- piperazine (401mg, 4.00mmol), potassium carbonate (276mg, 2.00mmol), and DMF (3mL) was stirred and heated at HO⁰C for 24h. After cooling to rt, the mixture was poured into brine (1OmL) and extracted with EtOAc (3 x 1OmL). The combined organic extracts were extracted with aqueous HCl (1 N, 2 x 2OmL). The acidic extracts were basified by aqueous NaOH until pH>10. The basified aqueous solution was extracted with EtOAc (2 x 3OmL). The extracts were then washed with H₂O (3 x 2OmL) and brine (2OmL), dried over MgSO₄, filtered and concentrated in vacuo to give the title compound as yellow oil. ¹H NMR (CD₃OD₃ 400 MHz): δ = 2.22 (s, 3 H), 2.48 (t, 4 H, J= 5.0 Hz), 3.16 (t, 4 H, J= 5.2 Hz), 7.16 - 7.18 (m, 1 H), 7.27 (t, 1 H, J= 8.2 Hz), 7.46 - 7.49 (m, 1 H), 7.57 (t, 1 H, J= 2.2 Hz). MS (ES+): m/z 222.26 (100) [MH⁺]. HPLC: t_κ = 1.55 min (ZQ2000, polar_5 min). [716] EXAMPLE 251: 4-{4-[3-ChIoro-5-(4-methylpiperazin-l-yl)-phenyl- aminol-TH-pyrrolotZ^-rflpyriinidin-β-ylJ-Sjδ-dihydro^iϊ-pyridine-l-carboxylic acid tert-butyl ester.

[717] A mixture of 4-(4-chloro-7H-pyrrolo[2,3 -d]pyrimidin-6-yl)-3 ,6-dihydro-2H- pyridine-1-carboxylic acid tert-butyl ester (88.0mg, 0.263mmol), 3-chloro-5-(4- methylpiperazin-l-yl)-phenylamine (71.2mg, 0.316mmol), trifluoroacetic acid (203μL, 2,63mmol), and DMF (2mL) was stirred in a sealed tube at 70⁰C for 18h. The mixture was concentrated in vacuo, sodium bicarbonate (221mg, 2.63mmol), di-tert-butyldicarbonate (86.1mg, 0.394mmol), and DMF (2mL) were added to the residue, and the resulting mixture was stirred at rt under N₂ for 16h. After that time, the mixture was filtered, and the filtrate was concentrated in vacuo and submitted for MS-directed purification. One obtained the title compound as light-brown solid. ¹H NMR (CD₃OD, 400 MHz): δ = 1.50 (s, 9 H), 2.57 (brs, 2 H), 2.86 (s, 3 H), 3.29 (brs, 4 H), 3.46 (brs, 4 H), 3.67 (brs, 2 H), 4.13 (brs, 2 H), 6.29 (brs, 1 H), 6.68 (s, 1 H), 6.74 (s 1 H), 7.44 (s, 1 H), 7.47 (s, 1 H), 8.28 (s, 1 H). MS (ES+): m/z 523.99/525.95(100/40) [MH⁺]. HPLC: fc(polar-5 mins) = 2.28 min (ZQ2000, polar_5 min). [718] 3-Chloro-5-(4-methylpiperazin-l-yl)-phenylamine

[719] The title compound was obtained by following the procedure for the reduction of 5-nitro-2,3-dihydroisoindol-l-one with iron powder, but using l-(3-chloro-5- nitrophenyl)-4-methylpiperazine. ¹H NMR (OMSO-d₆, 400 MHz): δ = 2.33 (s, 3 H), 2.58 (bra, 4 H), 3.11 (brs, 4 H), 5.21 (bra, 2 H), 6.05 - 6.06 (m, 2 H), 6.12 - 6.13 (m, 1 H). MS (ES+): m/z 226.17/228.19 (100/33) [MH⁺]. HPLC: t_R = 1.42 min (ZQ2000, polar_5 min). [720] l-(3-Chloro-5-nitrophenyl)-4-methylpiperazine

[721] The title compound was obtained by following the procedure for the halide displacement of 3-fluoronitrobenzene with methylpiperazine, but using l,3-dichloro-5- nitrobenzene and conducting the reaction at 130⁰C. ¹H NMR (CDCl₃, 400 MHz): δ = 2.34 - 2.40 (m, 3 H), 2.56 - 2.59 (m, 4 H), 3.30 - 3.33(m, 4 H), 7.11 - 7.15 (m, 1 H), 7.61 - 7.64 (m, 2 H). MS (ES+): m/z 256.12/258.07 (100/33) [MH⁺]. HPLC: t_R = 1.94 min (ZQ2000, polar_5 min).

[722] EXAMPLE 252: 4-{4-[3-ChIoro-5-(4-methylpiperazin-l-yl)-phenyl- amino]-7H-pyrrolo[2,3-rf]pyrimidin-6-yl}-3,6-dihydro-2H^:-pyridine-l-carboxylic acid tert-butylaraide.

[723] A mixture of 4-(4-chloro-7H-pyrrolo[2,3-d]pyrimidin-6-yl)-3,6-dihydro-2H- pyridine-1-carboxylic acid fe7-/-butyl ester (88.0mg, 0.263mmol), 3-chloro-5-(4- meuiylpiperazin-l-yl)-phenylamine (71.2mg, 0.316mmol), trifluoroacetic acid (243μL, 3.16mmol), and DMF (2mL) was stirred in a sealed tube at 80⁰C for 16h. After cooling, NJV- diisopropylethylamine (550μL, 3.16mmol) was added, and the mixture turned into a dark clear solution. Into above solution was added tert-butyl isocyanate (36.0μL, 0.316mmol) and the solution was stirring at rt for Ih. After that time, the mixture was concentrated in vacuo to obtain dark-brown oil that was submitted for MS-directed purification to obtain a light-brown oil. Further purification by ΗPLC gave the title compound as an off-white powder. ¹H ΝMR (DMSO-^, 400 MHz): δ = 1.29 (s, 9 H), 2.23 (s, 3 H), 2.46 (t, 4 H, J= 4.6 Hz), 3.18 (t, 4 H, J= 4.8 Hz), 3.53 (t, 2 H, J= 5.4 Hz), 4.00 (brs, 2 H), 5.79 (s, 1 H), 6.43 (s, 1 H), 6.63 (d, 1 H, J= 1.6 Hz), 6.78 (s 1 H), 7.30 (s, 1 H), 7.75 (d, 1 H, J= 1.6 Hz), 8.32 (s, 1 H), 9.27 (s, 1 H),

11.98 (s, 1 H). MS (ES+): m/z 522.98/525.01(100/33) [MH⁺]. HPLC: & = 2.13 min

(ZQ2000, polar_5 min).

[724] EXAMPLE 253: 4-{4-[3-(2-Aminothiazol-4-yI)-phenyIamino]-7£r- pyrrolo[2,3-rf]pyrimidin-6-yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid fert-butyl ester.

[725] The title compoimd was obtained following the General method for the reaction of amines with tert-butyl 4-(4-chloro-7H-pyrrolo[2,3-rf]pyrimidin-6-yl)-3,6- dihydropyridine-1 (2H)-carboxylate, using 4-(3 -aminophenyl)-thiazol-2-ylamine. ¹H NMR (CD₃OD, 400 MHz): δ = 1.52 (s, 9 H), 2.58 (brs, 2 H), 3.68 (bis, 2 H), 4.13 (bis, 2 H), 6.30 (brs, 1 H), 6.65 (s, 1 H), 6.86 (s, 1 H), 7.36 - 7.40 (m, 1 H), 7.52 - 7.54 (m, 1 H), 7.65 - 7.67 (m, 1 H), 8.07 - 8.08 (m, 1 H), 8.24 (s, 1 H). MS (ES+): m/z 489.94 (38) [MH⁺]. HPLC: fo = 2.71 min (ZQ2000, polar_5 min). [726] 4-(3-AminophenyI)-thiazoI-2-ylamine

[727] The title compound was obtained by following the procedure for the reduction of 5-nitro-2,3-dihydroisoindol-l-one with iron powder, but using 4-(3-nitrophenyl)- thiazol-2-ylamine. ¹H NMR (DMSO-<4, 400 MHz): δ = 5.03 (brs, 2 H), 6.43 (d, 1 H, J= 7.2 Hz), 6.75 (s, 1 H), 6.89-7.00 (m, 5 H). MS (ES+): m/z 192.24 (100) [MH⁺]. HPLC: t_R = 1.45 min (ZQ2000, polar_5 min). [728] 4-(3-NitrophenyI)-thiazol-2-ylamine

O₂N ^S

[729] A solution of 3-nitrophenacyl bromide (244mg, 1.OOmmol) and thiourea

(76.1mg, 1. OOmmol) in DMF (2mL) was stirred at 60⁰C for 16h. The mixture was concentrated in vacuo to obtain a yellow solid that was then washed with H₂O and dried to yield a yellow solid (206mg). The solid was dissolved in DMSO and purified by SCX column (4 x 6mL capacity), eluted with CH₂Cl₂ (4 x 6mL), MeOH (4 x 12mL) and then released by NH₃ (7 N in MeOH, 4 x 6mL) to give a light-yellow solid of 4-(3-aminophenyl)- thiazol-2-ylamine. ¹H NMR (DMSO-d₆, 400 MHz): δ = 7.24 (brs, 2 H), 7.35 (s, 1 H), 7.65 - 7.69 (m, 1 H), 8.10 - 8.13 (m, 1 H), 8.23 - 8.26 (m, 1 H), 8.62 (t, 1 H, J= 1.8 Hz). MS (ES+): m/z 223.12 (45) [MH⁺]. HPLC: t_R = 2.82 min (ZQ2000, polar_5 min). The combined CH₂Cl₂ and MeOH solution was concentrated in vacuo to give a yellow solid of 4-(3- aminophenyl)-lH-imidazole-2-thiol. ¹H NMR (DMSO-J₆, 400 MHz): δ = 7.75 (t, 1 H, J= 8.0 Hz), 8.01 (d, 1 H, J= 0.8 Hz), 8.17 - 8.20 (m, 1 H), 8.35 - 8.37 (m, 1 H), 8.56 (d, 1 H, J= 1.6 Hz), 8.72 (t, 1 U, J= 1.8 Hz), 12.56 (s, 1 H). MS (ES+): m/z 222.12 (15) [MH⁺]. HPLC: t_R = 2.97 min (ZQ2000, polar_5 min).

[730] EXAMPLE 254: tert-Butyl 4-[4-(3-iodo-4-methoxyphenylamino)-7#- pyrrolo [2,3-d\ pyrimidin-6-yl] -3 ,6-dihydro-2/Z-py ridine-1 -carboxylate.

[731] 3-Iodo-4-methoxyaniline (0.67Og, 2.0mmol) was added to a solution of /ert- butyl 4-(chloro-7H-pyrrolo[2,3-(/jpyrimidin-6-yl)-3,6-diliydro-2H-pyridine-l-carboxylate (0.598g, 2.4mmol) in n-butanol (1OmL). The mixture was heated to 95°C for 15h. The solvent was removed and the residue was purified by silica gel chromatography (5% MeOH in dichloromethane) to afford the title compound. ¹H-NMR (DMSO-d₆, 400 MHz): δ = 1.43 (s, 9 H), 2.46 (m, 2 H), 3.56 (m, 2 H), 3.80 (s, 3 H), 4.03 (m, 2 H), 6.38 (s, 1 H), 6.72 (s, 1 H), 7.00 (d, J= 9.2 Hz, 1 H), 7.85 (dd, /= 2.8, 8.8 Hz, 1 H), 8.34 (s, 1 H), 9.27 (s, 1 H), 11.93 (s, 1 H). MS (ES+): m/z 547.91 [MH⁺]. HPLC: t_κ = 3.39 min (ZQ2000, polar_5min). [732] EXAMPLE 255: ter^ButyI 4-[4-(3-iodophenylamino)-7H-pyrrolo[2,3- rf]pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylate.

[733] The title compound was prepared following the above procedure, but using 3- iodoaniline. MS (ES+): m/z 517.91. HPLC: t_R = 3.75 min (ZQ2000, polar_5min).

[734] EXAMPLE 256: tert-Butyl 4-{4-[3-(lH-pyrrol-2-yl)phenyIamino]-7H- pyrrolo[2,3-rf]pyrimidin-6-yl}-3,6-dihydro-2_JH^r-pyridine-l-carboxylate.

[735] To a stirred solution of tert-butyl 4-[4-(3-iodophenylamino)-7H-pyrrolo[2,3- cf]pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylate (77.6mg, 0.15mmol), N-Boc-2- pyrrolylboronic acid (47.5mg, 0.225mmol) and potassium carbonate (41.5mg, 0.3mmol) in dioxane/water (4:1) (1.OmL) was added PdCl₂(dppfyCH₂Cl₂ (12.2mg, 0.015mmol). The mixture was heated at reflux for 18h. Solvents were removed in vacuo and the residue was dissolved in DMF (∞2mL). The DMF solution was filtered and purified by HPLC to afford the title compound. ¹H-NMR(CD₃OD, 400 MHz): δ = 1.50 (s, 9 H), 2.53 (m, 2 H), 3.64 (m, 2 H), 4.11 (m, 2 H), 6.16 (t, J= 2.8 Hz, 2 H), 6.26 (s, 1 H), 6.48 (dd, J= 1.2, 3.6 Hz, 1 H), 6.60 (s, 1 H), 6.81 (dd, J= 1.2, 2.8 Hz, 1 H), 7.31 (s, 1 H), 7.33 (s, 1 H), 7.42-7.45 (m, 1 H), 7.87 (s, 1 H), 8.21 (s, 1 H). MS (ES+): m/z 457.08 [MH⁺]. HPLC: *_R = 3.15 min (ZQ2000, polar_5min).

[736] EXAMPLE 257: tert-Butyl 4-[4-(3-thiophen-3-ylphenylammo)-7H- pyrroIo[2,3-rf]pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylate.

[737] The title compound was prepared following the procedure for tert-butyl 4-{4-

[3 -(lH-pyrrol-2-yl)phenylamino]-7H-pyrrolo[2,3-(/]pyrimidin-6-yl} -3 ,6-dihydro-2H- pyridine-1-carboxylate, but using 3-thienylboronic acid. ¹H-NMR (CD₃OD, 400 MHz): δ = 1.50 (s, 9 H), 2.56 (m, 2 H), 3.67 (m, 2 H), 4.13 (m, 2 H), 6.30 (s, br, 1 H), 6.66 (s, 1 H), 7.37- 7.42 (m, 2 H), 7.47-7.50 (m, 2 H), 7.63-7.66 (m, 2 H), 8.01-8.02 (m, 1 H), 8.23 (s, 1 H). MS (ES+): m/z 474.04 [MH⁺]. HPLC: t_κ = 3.58 min (ZQ2000, polar_5min). [738] EXAMPLE 258: tert-Butyl 4-{4-[3-(lH-pyrazol-4-yI)phenylamino]-7iZ- pyrrolo[2,3-rf]pyrimidin-6-yI}-3,6-dihydro-2H-pyridine-l-carboxylate.

[739] The title compound was prepared following the procedure for tert-butyl 4- {4-

[3-(lH-pyrτol-2-yl)phenylamino]-7H-pyrrolo[2,3-d]pyrimidin-6-yl}-3,6-dihydro-2H- pyridine- 1-carboxylate, but using 4-(4,4,5,5-tetramethyl-[l,3,2]dioxaborolan-2-yl)-lH- pyrazole. ¹H-NMR (CD₃OD, 400 MHz): δ = 1.50 (s, 9 H), 2.57 (m, 2 H), 3.67 (m, 2 H), 4.14 (m, 2 H), 6.29 (s, br, 1 H), 6.66 (s, 1 H), 7.33-7.39 (m, 2 H), 7.58 (dt, J= 2.0, 7.2 Hz, 1 H), 7.92 (d, J= 1.2 Hz, 1 H), 7.93-8.00 (m, 2 H), 8.23 (s, 1 H). MS (ES+): m/z 458.03 [MH⁺]. HPLC: t_R = 2.70 min (ZQ2000, polar_5min).

[740] EXAMPLE 259: tert-Butyl 4-{4-[4-methoxy-3-(lH-pyrrol-2-yl)- phenylamino]-7iϊ-pyrrolo[2,3-d]pyrimidin-6-yI}-3,6-dihydro-2H-pyridine-l-carboxyIate.

[741] To a stirred solution of tert-bυtyl 4-[4-(3-iodo-4-methoxyphenylamino)-7H- pyrrolo[2,3-cf]pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylate (82.1mg, 0.15mmol), N-Boc-2-pyrrolylboronic acid (47.5mg, 0.225mmol) and potassium carbonate (41.5mg, 0.3mmol) in dioxane/water (4:1) (1.OmL) was added PdCl₂(dppf)-CH₂Cl₂ (12.2mg, 0.015mmol). The mixture was heated at reflux for 18h. Solvents were removed and the residue was dissolved in DMF («2mL). The DMF solution was filtered and sent to mass- directed HPLC purification. The pyrrole-Boc-protected product obtained was stirred with NaOH (s, 369mg) in 9mL of methanol at rt for 17h. The solvent was removed and the residue was dissolved in DMF (∞l .5mL) and purified by HPLC purification to give the title compound. ¹H-NMR (DMSO-d₆, 400 MHz): δ = 1.43 (s, 9 H), 2.46 (m, 2 H), 3.56 (m, 2 H), 3.87 (s, 3 H), 4.03 (m, 2 H), 6.11 (q, J= 2.4 Hz, 1 H), 6.37 (s, br, 1 H), 6.49 (s, 1 H), 6.71 (s, 1 H), 6.81 (q, J= 2.4 Hz, 1 H), 7.04 (d, J= 9.2 Hz, 1 H), 7.63 (d, J= 6.0 Hz, 1 H), 7.92 (d, J = 2.4 Hz, 1 H), 8.20 (d, J= 4.4 Hz, 1 H), 9.22 (s, 1 H), 10.91 (s, 1 H), 11.89 (s, 1 H). MS (ES+): m/z 487.04 [MH⁺]. HPLC: t_R = 2.96 min (ZQ2000, polar_5min). [742] EXAMPLE 260: tert-Butyl 4-[4-(4-raethoxy-3-thiophen-3-yIphenyI- amino)-7H-pyrrolo[2,3-rf]pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylate.

[743] To a stirred solution of tert-butyl 4-[4-(3-iodo-4-methoxyphenylamino)-7H- pyrrolo[2,3-rf]pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylate (82.1mg, 0.15mmol), 3-thienylboronic acid (28.8mg, 0.225mmol) and potassium carbonate (41.5mg, 0.3mmol) in dioxane/water (4:1) (1.OmL) was added [l,r-tø(diphenylphosphino)ferrocene]dichloro- palladium(II), complex with dichloromethane (1:1) (12mg, 0.015mmol). The resulting mixture was bubbled N₂ for 5min and then heated at reflux for 16h. After cooled to rt, the solvents were removed under reduced pressure. The residue was dissolved in DMF (2mL). The DMF solution was filtered and purified by HPLC to give the title compound. ¹H-NMR (DMSO-d₆, 400 MHz): δ = 1.43 (s, 9 H), 3.56 (m, 2 H), 3.82 (s, 3 H), 4.03 (m, 2 H), 6.38 (s, br, 1 H), 6.73 (s, 1 H), 7.09 (d, J= 9.2 Hz, 1 H), 7.45 (dd, J= 0.8, 5.2 Hz, 1 H), 7.60 (dd, J= 2.8, 4.8 Hz, 1 H), 7.76 (m, 1 H), 7.80 (dd, J= 2.8, 8.8 Hz, 1 H), 7.94 (d, J= 2.8 Hz, 1 H), 8.22 (s, 1 H), 9.26 (s, 1 H), 11.90 (s, 1 H). MS (ES+): m/z 504.05 [MH⁺]. HPLC: t_R = 3.22 min (ZQ2000, polar_5min).

[744] EXAMPLE 261: tert-Butyl 4-[4-(4-hydroxy-3-thiazol-5-ylphenyIamino)-

7iϊ-pyrrolo [2,3-rf] pyrimidin-6-yl] -S_jό-dihydro^JΪ-pyridine-l-carboxylate.

[745] 4-Amino-2-thiazol-5-ylphenol (70.0mg, 0.364mmol) was added to a solution of tert-bu1yl 4-(chloro-7H-pyrrolo[2,3-£f|pyrimidin-6-yl)-3,6-dihydro-2H-pyridine-l- carboxylate (192mg, 0.546mol) in n-butanol (2.OmL). The reaction was stirred at 120°C for 14h. The solvent was removed and the residue was dissolved in DMF. The DMF solution was filtered and purified by HPLC to give the title compound. ¹H-NMR (DMSOd₆, 400 MHz): δ = 1.43 (s, 9 H), 2.46 (m, 2 H), 3.56 (t, J= 5.6 Hz, 2 H), 4.04 (s, 2 H), 6.38 (s, br, 1 H), 6.70 (s, 1 H), 6.97 (d, J= 8.8 Hz, 1 H), 7.70 (dd, J= 2.4, 8.8 Hz, 1 H), 8.07 (d, J= 2.4 Hz, 1 H), 8.22 (s, 1 H), 8.32 (s, 1 H), 9.05 (s, 1 H), 9.23 (s, 1 H), 10.25 (s, br, 1 H), 11.88 (s, 1 H). MS (ES+): m/z 490.94 (MH⁺). HPLC: t_R = 2.51 min (ZQ2000, polar_5min). [746] 4-Amino-2-thiazol-5-yIphenoI

[747] 4-Nitro-2-thiazol-5-ylphenol (lOOmg, 0.4mmol) in methanol (5mL) was hydrogenated in the presence of 10% Pd/C (80mg) for 16h. The reaction mixture was filtered through a Celite pad. The filtrate was concentrated in vacuo to afford the title compound, which was used directly in the next step without purification. ¹H-NMR (CD₃OD, 400 MHz): δ = 7.18 (d, J= 8.8 Hz, 1 H), 7.39 (dd, J= 2.4, 8.8h z, 1 H), 7.91 (d, J= 2.8 Hz, 1 H), 8.91 (s, 1 H), 9.97 (s, 1 H). MS (ES+): m/z 193.14 [MH⁺]. HPLC: fe = 0.48 min (ZQ2000, polar_5min). [748] 4-Nitro-2-thiazol-5-ylphenol

[749] A mixture of 5-(2-methoxy-5-nitrophenyl)thiazole (156mg, 0.660mmol) and anhydrous sodium sulfide (309mg, 3.96mmol) in N-methylpyrrolidinone (2mL) was heated at 16O⁰C for 2h. After cooling to rt, the solvent was removed in vacuo, and the residue was partitioned between water (5mL) and dichloromethane (2OmL). The organic phase was separated, dried over MgSO₄, and purified by silica gel chromatography (3% MeOH in dichloromethane) to afford the title compound. ¹H-NMR (CDCl₃, 400 MHz): δ = 7.18 (d, J=

9.2 Hz, 1 H), 8.08 (dd, J= 1.6, 9.2 Hz, 1 H), 8.45 (s, 1 H), 8.52 (d, J= 2.4 Hz, 1 H), 8.86 (s, 1

H), 11.95 (s, br, 1 H). MS (ES+): m/z 223.14 [MH⁺]. HPLC: t_κ = 2.68 min (ZQ2000, polar_5min).

[750] 5-(2-Methoxy-5-nitrophenyl)thiazole

[751] N₂ was bubbled through a solution of 2-iodo-4-nitroanisole (2.8g, 10.Ommol), thiazole (2.55g, 30.0mmol), potassium acetate (1.47g, 15.0mmol), and tetrakis(triphenyl phosphine)palladium(O) (0.81g, 0.70mmol) in DMF (15mL) for lOmin. The mixture was then heated to 100⁰C and stirred overnight. Solvent was removed under reduced pressure, and the residue was purified by silica gel chromatography (dichloromethane:MeOH = 96:4) to afford the title compound. ¹H-NMR (CDCl₃, 400 MHz): δ = 4.08 (s, 3 H), 7.09 (d, J= 9.2 Hz, 1 H), 8.25 (dd, J= 2.8, 9.2 Hz, 1 H), 8.37 (s, 1 H), 8.54 (d, J= 3.2 Hz, 1 H), 8.88 (s, 1 H). MS (ES+): m/z 237.13 [MH⁺]. HPLC: t_R = 3.07 min (ZQ2000, polar_5min). [752] EXAMPLE 262: fert-Butyl 4-[4-(3-chIoro-5-thiazol-5-ylphenylamino)-

7H-pyrrolo[2,3-rf]pyrimidin-6-yI]-3,6-dihydro-2H-pyridine-l-carboxyIate.

[753] The title compound was obtained following the General method for the reaction of amines with tert-butyl 4-(4-chloro-7H-pyrrolo[2,3-</]pyrimidin-6-yl)-3,6- dihydropyridine-l(2H)-carboxylate, using 3-chloro-5-thiazol-5-ylphenylamine. ¹H-NMR (CD₃OD, 400 MHz): δ = 1.50 (s, 9 H), 2.58 (m, 2 H), 3.67 (m, 2 H), 4.13 (s, 2 H), 6.30 (s, br, 1 H), 6.72 (s, 1 H), 7.35 (t, J= 1.6 Hz, 1 H), 8.05-8.07 (m, 2 H), 8.21 (d, J= 0.4 Hz, 1 H), 8.33 (s, 1 H), 9.00 (d, J= 0.8 Hz, 1 H). MS (ES+): m/z 508.81 (MH⁺, ³⁵Cl), 510.91 (MH⁺, ³⁷Cl). HPLC: ._R = 3.75 min (ZQ2000, polar_5min). [754] 3-ChIoro-5-thiazol-5-ylphenylamine

[755] To a solution of 5-(3-chloro-5-nitrophenyl)thiazole (0.12Og, 0.499mmol) in ethanol (5mL) was added tin dichloride (0.9555g, 4.986mmol). The mixture was stirred at 9O⁰C for 1.5h. After cooling to rt, sat. NaHCO₃ (aq) was added dropwise to adjust the pH to 9-10. The resulting suspension was filtered through a Celite pad. The filtrate was concentrated to dryness in vacuo to afford the title compound, which was used directly in the next step without purification. ¹H-NMR (CD₃OD, 400 MHz): δ = 6.67 (t, J= 2.0 Hz, 1 H), 6.85 (t, J= 1.6 Hz, 1 H), 6.88 (t, J= 1.6 Hz, 1 H), 8.10 (s, 1 H), 8.94 (s, 1 H). MS (ES+): m/z 211.10 (MH⁺, ³⁵Cl), 213.12 (MH⁺, ³⁷Cl). HPLC: t_R = 2.92 min (ZQ2000, polar_5min). [756] 5-(3-Chloro-5-nitrophenyl)thiazole

[757] N₂ was bubbled through a solution of 3,5-dichloronitrobenzene (0.384g,

2.00mmol), thiazole (0.204g, 2.40mmol), potassium acetate (0.294g, 3.00mmol), and tetrakis(triphenylphosphine)palladium(0) (0.16g, 0.14 mol) in DMF (5mL) for lOmin. The mixture was then heated to 12O⁰C and stirred for 17h. The solvents were removed in vacuo. The residue was purified by chromatography on silica gel (MeOH in methylene chloride: 1% to 5%) to afford the title compound. ¹H-NMR (CDCl₃, 400 MHz): δ = 7.88 (t, J= 2.0 Hz, 1 H), 8.20 (t, J= 2.4 Hz, 1 H), 8.22 (s, 1 H), 8.32 (t, J= 2.0 Hz, 1 H), 8.90 (s, 1 H). MS (ES+): m/z 241.04 (³⁵Cl, MH⁺), 243.00 (³⁷Cl, MH⁺). HPLC: fc = 3.35 min (ZQ2000, polar_5min). [758] EXAMPLE 263: tert-Butyl 4-{4-[3-(4-methyl-4H-[l,2,4]triazol-3-yl)- phenylamino]-7H-pyrroIo[2,3-rfIpyrimidin-6-yl}-3,6-dihydro-2jH^r-pyridine-l-carboxylate.

[759] The title compound was obtained following the General method for the reaction of amines with ter/-butyl 4-(4-chloro-7H-pyrrolo[2,3-^pyrimidin-6-yl)-3,6- dihydropyridine-1 (2H)-carboxylate, using 3-(4-methyl-4H-[l ,2,4]triazol-3-yl)-phenylamine. ¹H-NMR (CD₃OD, 400 MHz): δ = 1.50 (s, 9 H), 2.58 (m, 2 H), 3.67 (m, 2 H), 3.89 (s, 3 H), 4.13 (m, 2 H), 6.30 (s, br, 1 H), 6.73 (s, 1 H), 7.41 (dt, J= 1.2, 7.6 Hz, 1 H), 7.54 (t, J= 7.6 Hz, 1 H), 7.93 (dq, J= 0.8, 8.4 Hz, 1 H), 8.26 (s, 1 H), 8.30 (t, J= 1.6 Hz, 1 H), 8.57 (s, 1 H). MS (ES+): m/z 473.01 [MH⁺]. HPLC: fe = 2.60 min (ZQ2000, polar_5min). [760] EXAMPLE 264: tert-Butyl 4-[4-(lH-indol-4-ylamino)-7H-pyrrolo[2,3- d\ pyrimidin-6-yl] -3,6-dihydro-2.ff-pyridine-l-carboxylate.

[761] The title compound was obtained following the General method for the reaction of amines with tert-butyl 4-(4-chloro-7H-pyrrolo[2,3-rf]pyrimidin-6-yl)-3,6- dihydropyridine-l(2H)-carboxylate, using 4-aminoindole. ¹H-NMR (CD₃OD, 400 MHz): δ = 1.49 (s, 9 H), 2.42 (m, 2 H), 3.61 (m, 2 H), 4.09 (m, 2 H), 6.22 (br, 2 H), 6.39 (dd, J= 1.2, 2.8 Hz, 1 H), 7.13-7.18 (m, 2 H), 7.21 (d, J= 3.2 Hz, 1 H), 7.32-7.34 (m, 1 H), 8.07 (s, 1 H). MS (ES+): m/z 431.09 [MH⁺]. HPLC: t_κ = 2.47 min (ZQ2000, polar_5min). [762] EXAMPLE 265: 4-[4-(Naphthalen-l-ylamino)-7iϊ-pyrroIo[2,3-rf]- pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester.

[763] A suspension containing naphthalen-l-yl-[6-(l,2,3,6-tetrahydropyridin-4-yl)-

7H-pyrrolo[2,3-dJpyrirnidin-4-yl]-amine (120mg, 0.35mmol), di-tert-butyldicarbonate (77mg, O.35mmol) and NN-diisopropylethylamine (122μL, OJOmmol) in anhydrous NN- dimethylformamide (2mL) was stirred overnight at rt. The reaction mixture was poured into saturated NaHCO₃ solution (5OmL) and extracted with EtOAc (3x40mL). The combined organics were washed with brine (3x10OmL), dried (MgSO₄), filtered and concentrated. Flash chromatography (2 to 4% MeOH in DCM) gave the title compound as a white solid. ¹H NMR (DMSO-d₆, 400 MHz): δ = 8.28 (IH, s), 8.14-8.12 (2H, m), 7.94 (IH, d, J= 7.5Hz), 7.87 (IH, d, J= 7.4 Hz), 7.67 (IH, d, J= 7.1 Hz), 7.56-7.48 (3H, m), 6.13 (IH, s), 5.35 (IH, s), 4.02 (2H, s), 3.52 (2H, s), 2.21 (2H, s), 1.47 (9H, s); MS (ES+): m/z 442.08 [MH⁺], HPLC: /_R = 2.96 min (MicromassZQ, polar_5min).

[764] Naphthalen-l-yl-[6-(l,2,3,6-tetrahydropyridin-4-yl)-7H-pyrroIo[2,3- d] py rimidin-4-yI] amine

[765] A sealed tube containing a solution of 4-(4-chloro-7H-pyrrolo[2,3-d]- pyrimidin-6-yl)-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester (250mg, 0.75mmol), 1-naphthylamine (160mg, 1.12mmol) and trifluoroacetic acid (287μL, 3.73mmol) in 2,2,2-trifluoroethanol (5mL) was heated at 8O⁰C and maintained at this temperature overnight. The product was poured into saturated NaHCO₃ solution (5OmL) and the precipitate was filtered off, giving the title compound as an off-white solid. ¹H NMR (DMSO-d₆, 400MHz): δ = 9.48 (IH, s), 8.14-7.92 (3H, m), 7.82 (IH, d, J= 8.0Hz), 7.64 (IH, d, J= 7.2 Hz), 7.61-7.44 (3H, m), 6.40 (IH, s), 4.02 (2H, brs), 3.51 (2H, brs), 2.89 (2H, brs); MS (ES+): m/z 342.11 [MH⁺], HPLC: t_R = 1.71 min (MicromassZQ, polar_5min). [766] EXAMPLE 266: 4-[4-(Naphthalen-l-yIamino)-7fi-pyrrolo[2,3-rfJ- pyrimidin-6-yl]-3,6-dihydro-2i?-pyridine-l-carboxyIic acid fertf-butylamide.

[767] A suspension containing naphthalen-1 -yl-[6-( 1 ,2,3 ,6-tetrahydropyridin-4-yl)-

7H-pyrrolo[2,3-Gdpyrimidin-4-yl]-amine (120mg, 0.35mmol), fer/-butyl isocyanate (35mg, 0.35mmol) and NN-diisopropylethylamine (122μL, 0.70mmol) in anhydrous NN- dimethylformamide (2mL) was stirred overnight at rt. The reaction mixture was poured into saturated NaHCO₃ solution (5OmL) and extracted with EtOAc (3x50ml). The combined organics were washed with brine (3x50mL), dried (MgSO₄), filtered and concentrated. Flash chromatography (2 to 4% MeOH in DCM) gave the title compound as a white solid. ¹H NMR (DMSO-d₆, 400MHz): δ = 8.13 (IH, s), 8.08-8.02 (2H, m), 7.89 (IH, d, J = 8.1Hz), 7.74-7.71 (IH, m), 7.63-7.54 (3H, m), 6.55 (IH, d, J= 8.3 Hz), 6.43 (IH, s), 5.83 (IH, s), 4.04 (2H, s), 3.55 (2H, t, J= 5.6 Hz), 2.42 (2H, s), 1.34 (9H, s); MS (ES+): m/z 441.08 [MH⁺], HPLC: t_R = 2.59 min (MicromassZQ, polar_5min).

[768] EXAMPLE 267: 4-[4-(6-Oxo-l-phenyl-l,6-dihydropyridin-3-yIamino)-

7/7-pyrrolo [2,3-rf] pyrimidin-o-ylJ-Sjo-dihydro^H-pyridine-l-carboxylic acid tert-butyl ester.

[769] A mixture of 4-(4-chloro-7H-pyrrolo[2,3-rf]pyrimidin-6-yl)-3,6-dihydro-2H- pyridine-1-carboxylic acid tert-bniyl ester (75mg, 0.22mmol) and 5-amino-l-phenyl-lH- pyridin-2-one (50mg, 0.27mmol) in 1-butanol (3mL) was heated at 120°C overnight, LC-MS showed the desired product together with some de-Boc product. After the mixture was cooled to rt, it was diluted with methylene chloride (3mL), then N^V-diisopropylethylamine (0. ImL, O.όmmol) and di-tert-butyldicarbonate (49mg, 0.22mmol) were added. The resulting mixture was stirred at rt for 30min. The mixture was diluted with EtOAc (3OmL), then washed with brine (2OmL), and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was crystallized with EtOAc/Hexane to give the title compound as a green solid. LC-MS (ES, Pos.): 485 [MH⁺], and ¹H NMR (DMSO-d₆, 400 MHz): δ 1.43 (s, 9H), 2.50 (m, 2H), 3.56 (m, 2H), 4.04 (m, 2H), 6.39 (s, IH), 6.56 (d, J= 9.7 Hz, IH), 6.66 (s, IH), 7.39-7.57 (m, 5H), 7.81 (dd, J= 9.7, 2.7 Hz, IH), 8.17 (s, IH), 8.34 (d, J= 2.7 Hz, IH), 9.17 (s, IH), 11.94 (br s, IH).

[770] 5-Amino-l-phenyl-lH-pyridin-2-one

[771] To a suspension of 5-nitro-l-phenyl-lH-pyridin-2-one (60mg, 0.28mmol) in ethyl acetate (2mL) and ethanol (2mL) was added 5% Pd-C (10mg), the resulting mixture was stirred under hydrogen atmosphere for 3h. The catalyst was removed by filtration, and the filtrate was concentrated to give the title compound as a green oil. The product was used to next step without further purification. LC-MS (ES, Pos.): 187 [MH⁺], and ¹H NMR (CDCl₃, 400 MHz): δ = 3.09 (br s, 2H), 6.60 (d, J= 9.6 Hz, IH), 6.82 (d, J= 3.0 Hz, IH), 7.12 (dd, J = 9.6, 3.0 Hz, IH), 7.37-7.41 (m, 3H), 7.45-7.49 (m, 2H). [772] 5-Nitro-l-phenyl-lH-pyridin-2-one

[773] [Ref. Mederski, W.W.K.R., et al Tetrahedron, 1999, 55, 12757-12770.] To a solution of 2-hydroxy-5-nitropyridine (1.07g, 7.64mmol) in dry methylene chloride (5OmL) were added phenylboronic acid (1.86g, 15.3mmol), cupric acetate (1.71g, 9.41mmol), pyridine (1.2mL, 15.3mmol), triethylamine (2.ImL, 15.3mmol) and activated 4A molecular sieves (2g). The resulting mixture was stirred in air at rt for 2d. The mixture was then filtered through celite and washed with methylene chloride. The crude material was purified by silica gel chromatography, eluting with CH₂Cl₂ : EtOAc (85:15) to give the title compound as a white solid. LC-MS (ES, Pos.): 217 [MH⁺], and ¹H NMR (CDCl₃, 400 MHz): δ = 6.67 (d, J= 10.1 Hz, IH), 7.39-7.42 (m, 2H), 7.53-7.58 (m, 3H), 8.17 (dd, J= 10.1, 3.1 Hz, IH), 8.67 (d, J= 3.1 Hz, IH).

[774] EXAMPLE 268: 4-[4-(6-Oxo-l-phenyl-l,6-dihydropyridin-3-ylamino)-

7H-pyrrolo[2,3-rf|pyriraidin-6-yI]-3,6-dihydro-2H-pyridine-l-carboxylic acid fert- butylamide.

[775] A mixture of 4-(4-chloro-7H-pyrrolo[2,3-d]pyrimidin-6-yl)-3,6-dihydro-2H- pyridine-1-carboxylic acid tert-butyl ester (54.5mg, 0.163mmol), 5-amino-l-phenyl-lH- pyridin-2-one hydrochloride (43.5mg, 0.195mmol), dimethyl sulfoxide (3mL) and trifluoroacetic acid (125 μl, 1.63mmol) in a sealed tube was heated at 100°C overnight. The mixture was concentrated in vacuo and was charged with N^V-dimethylformamide (2mL), triethylamine (272μL, 1.95mmol) and tert-butyl isocyanate (20.4 μl, 0.179mmol). Tlie above mixture was stirred at rt for 1.5h, concentrated in vacuo, and partitioned between water/EtOAc (10mL/15mL). The aqueous phase was extracted with EtOAc (2x15mL), and the combined organic phase was washed with brine (1OmL), concentrated in vacuo, and dissolved in DMSO/MeOH for submission for MS-directed purification, which gave the title compound as beige solid. ¹H ΝMR (CD₃OD, 400 MHz): δ = 1.46 (s, 9 H), 2.67 (brs, 2 H), 3.69 - 3.72 (m, 2 H), 4.16(brs, 2 H), 6.41 (brs, 1 H), 6.72 (s, 1 H), 6.79 (d, 1 H, J= 9.6 Hz), 7.56 - 7.68 (m, 5 H), 7.95 (dd, 1 H, J= 2.8 & 9.6 Hz), 8.27 (s, 1 H), 8.39 (d, I U, J= 2.4 Hz), 8.64 (s, 1 H). MS (ES+): m/z 484.09 (100) [MH⁺]. HPLC: fe = 2.44 min (ZQ2000, polar_5 min).

[776] 5-Amino-l-phenyI-lfZ-pyridin-2-one, hydrochloride

[777] 5-(Benzhydrylideneamino)-l-phenyl-lH-pyridin-2-one (72.0 mg) was dissolved in tetrahydrofuran (3 ml), and aqueous HCl (2 M, 1.0 ml) was added while stirring at rt. The yellow color was faded. After 30 min, the reaction mixture was partitioned between aqueous HCl (1 M, 8 ml) and 40% EtOAc / hexane (15 ml). The aqueous layer was extracted with 40% EtOAc/hexane (15 ml), and the aqueous phase was then concentrated in vacuo to the title compound as beige foam. ¹H NMR (DMSO-J,,, 400 MHz): δ = 6.62 (d, 1 H, J= 10.0 Hz), 7.42 - 7.59 (m, 6 H), 7.90 (d, 1 H, J= 2.8 Hz), 10.34 (brs, 2 H). MS(ES+): m/z 187.22 (100) [MH⁺]. HPLC: t_R = 0.52 min (ZQ2000, polar_5min). [778] 5-(Benzhydrylideneamino)-l-phenyl-lH-pyridin-2-one

[779] Into a dried flask were added 5-bromo-l -phenyl- lH-pyridin-2-one (125 mg,

0.500 mmol), benzophenone imine (100 μl, 0.600 mmol), tris(dibenzylideneacetone)- dipalladium(O) (1.14 mg, 1.25 μmol), (R)-(+)-2,2'-bis(diρhenylphosphino)-l,r-binaphthyl (2.33 mg, 3.75 μmol), sodium tert-butoxide (67.2 mg, 0.700 mmol), and toluene (3 ml). The above mixture was flushed with N₂ for 5 min and was then heated at 80 °C under an atmosphere of nitrogen for 5 h. After that time, the heating was stopped and the reaction mixture was diluted with ethyl ether (30 ml), filtered and concentrated to obtain light-brown oil, which was then purified by chromatography on silica gel (10 g) eluting with 100 ml of 10%, 20%, 30% and 40%, and 300 ml 50% EtOAc/hexane to obtain the title compound as a yellow solid. ¹H NMR (CDCl₃, 400 MHz): δ = 6.45 (d, 1 H, J= 9.6 Hz), 6.89 (d, 1 H, J= 2.8 Hz), 7.00 (dd, 1 H, J= 2.8 & 10.4 Hz), 7.13 - 7.16 (m, 2 H), 7.19 - 7.22 (m, 2 H), 7.33 - 7.48 (m, 9 H), 7.69 - 7.72 (m, 2 H). MS(ES+): m/z 351.05 (100) [MH⁺]. HPLC: t_κ = 3.46 min (ZQ2000, polar_5mm).

[780] 5-Bromo-l~phenyl-l/7-pyridin-2-one

[781] Into a one-neck round-bottom flask were added 5-bromo-lH-pyridin-2-one

(696 mg, 4.00 mmol), phenylboronic acid (975 mg, 8.00 mmol), cupric acetate (1450 mg, 8.00 mmol), triethylamine (1120 μl, 8.00 mmol), pyridine (647 μl, 8.00 mmol), 4 A molecular sieves (1056 mg) and methylene chloride (24 ml). The flask was loosely capped and the above mixture was stirred at rt in the atmosphere of air for 20 h. The mixture was filtered through a celite pad, washed with CH₂Cl₂. After concentration in vacuo, a green oil (2100 mg) was obtained, which was then purified by chromatography on silica gel (64 g) eluting with 1000 ml 20%, 2000 ml 40% and 1000 ml 50% EtOAc/hexane to obtain the title compound as a light-yellow wax-like material. ¹H NMR (CDCl₃, 400 MHz): δ = 5.59 (d, 1 H, J= 9.6 Hz), 7.35 - 7.38 (m, 2 H), 7.41 - 7.46 (m, 2 H), 7.49 - 7.52 (m, 3 H). MS(ES+): m/z 250.06/252.02 (100/97) [MH⁺]. HPLC: fo = 2.71 min (ZQ2000, polar_5 min). [782] EXAMPLE 269: tert-Butyl 4-[4-(6-hydroxy-5-thiazol-5-ylpyridin-3- ylaminoJ^H-pyrroloPjS-rflpyrimidin-ό-yy-S_jό-dihydro-lH-pyridine-l-carboxylate.

[783] The title compound was obtained following the General method for the reaction of amines with tert-butyl 4-(4-chloro-7H-pyrrolo[2,3-J]pyrimidin-6-yl)-3,6- dihydropyridine-l(2H)-carboxylate, using 5-amino-3-thiazol-5-ylpyridin-2-ol. ¹H-NMR (DMSO-d₆, 400 MHz): δ = 1.43 (s, 9 H), 2.47 (m, 2 H), 3.57 (t, J= 5.6 Hz, 2 H), 4.04 (m, 2 H), 6.38 (br, 1 H), 6.66 (s, 1 H), 8.15 (s, 1 H), 8.23 (s, 1 H), 8.37 (d, J = 3.2 Hz, 1 H), 8.49 (s, 1 H), 9.04 (s, 1 H), 9.22 (s, 1 H), 11.96 (s, 1 H), 12.10 (s, br, 1 H). MS (ES+): m/z 491.98 [MH⁺]. HPLC: t_R = 2.49 min (ZQ2000, polar_5min). [784] 5-Amino-3-thiazol-5-ylpyridin-2-ol

[785] A solution of 5-nitro-3-thiazol-5-ylpyridin-2-ol (218mg, 0.977mmol) and

10% Pd/C (lOOmg) in methanol (5mL) was hydrogenated under latm at rt for 5h. The resulting mixture was filtered through a Celite pad. The filtrate was concentrated under reduced pressure to give 170mg of the title compound, which was used directly in the next step without purification. ¹H-NMR (DMSO-d₆, 400 MHz): δ = 4.38 (s, br, 2 H), 6.78 (d, J= 2.8 Hz, 1 H), 7.80 (d, J= 2.8 Hz, 1 H), 8.41 (s, 1 H), 8.97 (s, 1 H), 11.52 (s, br, 1 H). MS (ES+): m/z 194.15 [MH⁺]. HPLC: *_R = 0.49 and 0.90 min (ZQ2000, polar_5min). [786] 5-Nitro-3-thiazol-5-yIpyridin-2-ol

[787] N₂ was bubbled through a solution of 3-iodo-5-nitropyridin-2-ol (1.33g,

5.00mmol), thiazole (2.13g, 25.0mmol), potassium acetate (1.47g, 15.0mmol), and tetrakis(triphenylphosphine)palladium(0) (0.4g, 0.4mmol) in DMF (1OmL) for 10 min. The mixture was then heated to 12O⁰C and stirred for 17h. The solvents were removed in vacuo. The residue was stirred with methanol (5mL) and dichloromethane (1OmL) for 30min. The solids were collected by filtration, washed with dichloromethane (2mL) and water (3x8mL), and dried in vacuo to afford the title compound as an off-white solid. ¹H-NMR (DMSO-d₆, 400 MHz): δ = 8.74 (d, J= 2.8 Hz, 1 H), 8.77 (s, 1 H), 8.79 (d, J= 2.8 Hz, 1 H), 9.12 (s, 1 H), 13.26 (s, br, 1 H). MS (ES+): m/z 224.09 [MH⁺]. HPLC: t_R = 2.16 min (ZQ2000, polar_5min). [788] EXAMPLE 270: tert-Butyl 4-[4-(l-methyI-6-oxo-5-thiazol-5-yI-l,6- dihydropyridin-3-ylamino)-7_Jff-pyrrolo[2,3-rf]pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-

1-carboxylate.

[789] 5-Amino-l-methyl-3-thiazol-5-yl-lH-pyridin-2-one (99.0mg, 0.478mmol) was added to a solution of tert-butyl 4-(chloro-7H-pyrrolo[2,3-<f|pyrimidin-6-yl)-3,6-diliydro- 2H-pyridine~l-carboxylate (133mg, 0.398mmol) in 1-butanol (2.OmL). The reaction was stirred at 120⁰C for 15h. DMF (∞1.5mL) was added and the mixture was filtered. The filtrate was purified by ΗPLC to yield the title compound. ¹H-NMR (CD₃OD, 400 MHz): δ = 1.50 (s, 9 H), 2.57 (m, 2 H), 3.67 (m, 2 H), 3.73 (s, 3 H), 4.13 (m, 2 H), 6.30 (s, br, 1 H), 6.62 (s, 1 H), 8.21 (s, 1 H), 8.33 (d, J= 2.4 Hz, 1 H), 8.34 (d, J= 2.4 Hz, 1 H), 8.47 (s, 1 H), 8.99 (s, 1 H). MS (ES+): m/z 506.08 [MH⁺]. HPLC: /_R = 2.62 min (ZQ2000, polar_5min). [790] 5-Amino-l-methyl-3-thiazol-5-yI-lJϊ-pyridin-2-one

[791] To a solution of l-methyl-5-nitro-3-thiazol-5-yl-lH-pyridin-2-one (290mg,

1.22mmol) in ethanol (1OmL) was added SnCl₂ (2.342g, 12.22mmol). The mixture was stirred at 9O⁰C for 15h. After cooled to rt, sat. NaHCO₃ (aq) was added dropwise to the reaction to adjust the pH to 9-10. The resulting solution was filtered through a Celite pad. The filtrate was concentrated to dryness in vacuo to afford the crude product, which was used directly in the next step without purification. MS (ES+): m/z 208.21 [MH⁺]. HPLC: t_R = 1.47 min (ZQ2000, polar_5min). [792] l-MethyI-5-nitro-3-thiazol-S-yl-lH-pyridin-2-one

[793] N₂ was bubbled through a solution of 3-iodo-l -memyl-5-nitro-lH-pyridin-2~ one (840mg, 3.0mmol), thiazole (1280mg, 15.0mmol), potassium acetate (0.883g, 9.0mmol), and tetrakis(triphenylphosphine)palladium(0) (0.243g, 0.21mmol) in DMF (8mL) for lOmin. The mixture was then heated to 12O⁰C and stirred for 28h. The solvents were removed in vacuo. The black-colored residue was dissolved in a mixture of methanol (8mL) and methylene chloride (25OmL). Water (3OmL) and sat. NaHCO₃ (aq) (15mL) were added. Layers were separated and the aqueous phase was extracted with methylene chloride (3 x 8OmL). The combined organic phases were dried over MgSO₄, filtered, and concentrated under reduced pressure to «15mL. The product precipitated and was collected by filtration to afford the desired product as a black solid. ¹H-NMR (DMSO-d₆, 400 MHz): δ = 3.70 (s, 3 H), 8.79 (s, 1 H), 8.82 (d, J= 2.8 Hz, 1 H), 9.13 (s, 1 H), 9.29 (d, J= 3.2 Hz, 1 H). MS (ES+): m/z 238.15 [MH⁺]. HPLC: *_R = 2.33 min (ZQ2000, polar_5min). [794] 3-Iodo-l-methyI-5-nitro-l/7-pyridin-2-one

[795] A solution of 3-iodo-5-nitropyridin-2-ol (2.66g, lO.Ommol) in THF (3OmL) was cooled to -2O⁰C. NaH (60% dispersion in mineral oil, 0.60Og, 15.0mmol) was added cautiously in three portions. After being stirred for 30min at this temperature, methyl iodide (6.23mL, lOO.Ommol) was added dropwise through a syringe. The resulting mixture was allowed to warm to rt during a 30min period. Stirring was continued for 18h at rt. Water (15mL) was added with caution to quench the reaction. THF was removed under reduced pressure and methylene chloride (8OmL) was added to the aqueous phase. Layers were separated and the aqueous phase was extracted with methylene chloride (2x50mL). The combined organic phases were dried over MgSθ₄, filtered, and concentrated to afford the desired product as a yellow crystalline solid. ¹H-NMR (CDCl₃, 400 MHz): δ = 3.73 (s, 3 H), 8.65 (d, J= 2.8 Hz, 1 H), 8.74 (d, J= 2.8 Hz, 1 H). MS (ES+): m/z 280.96 [MH⁺]. HPLC: t_κ = 2.55 min (ZQ2000, polarjmin).

[796] EXAMPLE 271: tert-Butyl 4-(4-{3-[l-(2-dimethyIaminoethyI)-lH- imidazol-2-yI3phenyIamino}-7J3-pyrrolo[2,3-<iπpyrimidin-6-yl)-3,6-dihydro-2iϊ-pyridine- 1-carboxylate.

[797] The title compound was obtained following the General method for the reaction of amines with tert-butyl 4-(4-chloro-7H-pyrrolo[2,3-βTlpyrimidin-6-yl)-3_J6- dihydropyridine-l(2H)-carboxylate, usiαg 3-[l-(2-dimethylaminoethyl)-lH-iniidazol-2- yl]phenylamine. ¹H-NMR (CD₃OD, 400 MHz): δ = 1.50 (s, 9 H), 2.17 (s, 6 H), 2.58 (m, 2 H), 2.68 (t, J= 7.2 Hz, 2 H), 3.67 (m, 2 H), 4.13 (s, 2 H), 4.28 (t, J= 6.4 Hz, 2 H), 6.30 (s, br, 1 H), 6.71 (s, 1 H), 7.06 (d, J= 2.4 Hz, 1 H), 7.29 (dt, J= 2.4, 7.6 Hz, 1 H), 7.31 (d, J= 1.2 Hz, 1 H), 7.49 (t, J= 8.0 Hz, 1 H), 8.24 (dq, J= 0.8, 8.0 Hz, 1 H), 8.16 (t, J= 1.6 Hz, 1 H), 8.26 (d, J= 1.2 Hz, 1 H). MS (ES+): m/z 529.06 [MH⁺]. HPLC: % = 1.90 min (ZQ2000, polar_5min).

[798] 3- [l-(2-DimethylaminoethyI)-l/7-imidazol-2-yl] phenylamine

[799] Dimethyl-{2-[2-(3-nitrophenyl)imidazol-l-yl]ethyl}amine (88mg, 0.34mmol) in methanol (5mL) was hydrogenated in the presence of 10% Pd/C (80mg) for 16h. The reaction mixture was filtered through a Celite pad. The filtrate was concentrated in vacuo to afford the title compound, which was used directly in the next step without purification. ¹H- NMR (CDCl₃, 400 MHz): δ = 2.23 (s, 6 H), 2.63 (t, J= 7.2 Hz, 2 H), 4.13 (d, J = 7.2 Hz, 2 H), 6.72-6.75 (m, 1 H), 6.90-6.92 (m, 1 H), 6.96 (t, J- 2.0 Hz, 1 H), 7.08 (d, J= 1.2 Hz, 1 H), 7.11 (d, J= 1.2 Hz, 1 H), 7.22 (t, J= 7.6 Hz, 1 H). MS (ES+): m/z 231.22 [MH⁺]. HPLC: t_κ = 0.33 min (ZQ2000, polar_5min). [800] Dimethyl-{2-[2-(3-nitrophenyI)imidazoI-l-yI] ethyl}amine

[801] At rt and under N₂, to a solution of 2-(3-nitrophenyl)-lH-imidazole (0.189g,

1.OOmmol) and (2~bromoethyl)dimethylamine hydrobromide (0.28Og, 1.20mmol) in anhydrous DMF (5mL) was added NaH (60% in mineral oil, 160mg, 4.0mmol) in two portions with caution. The mixture was stirred at rt for 15h. Water (0.3mL) was added cautiously to quench the reaction. Solvent was removed in vacuo, and the residue was purified by silica gel chromatography (5% MeOH in dichloromethane) to afford the title compound. ¹H-NMR (CDCl₃, 400 MHz): δ = 2.24 (s, 6 H), 2.69 (t, J= 7.2 Hz, 2 H), 4.13 (d, J= 6.8 Hz, 2 H), 7.17 (d, J= 1.2 Hz, 1 H), 7.19 (d, J= 1.2 Hz, 1 H), 7.65 (t, J= 8.0 Hz, 1 H), 8.04(dt, J= 0.8, 8.0 Hz, 1 H), 8.28 (dq, J= 1.2, 8.4 Hz₅ 1 H), 8.56 (t, J= 1.6 Hz, 1 H). MS (ES+): m/z 261.17 [MH⁺]. HPLC: *_R = 0.46 min (ZQ2000, polar_5mm). [802] 2-(3-Nitrophenyl)-lH-imidazole

^•\

\ Il

NO,

[803] 3-Nitrobenzaldehyde (4.53g, 30.0mmol), 40% aqueous glyoxal solution

(23.9g, 165mmol), and sodium acetate (11.6g, 141mmol) were dissolved at rt in 9OmL of aqueous ammonium hydroxide solution (28-30 wt%) and 18OmL of methanol. The solution was stirred at rt for 16h. Solvents were removed in vacuo, and 8OmL of sat. NaHCO₃ (aq) was added to the residue. The aqueous solution was extracted with EtOAc (3x300mL). The combined organic phases were dried over MgSO₄, filtered, and concentrated to give a black oily residue, which was purified by silica gel chromatography (5% MeOH in CH₂Cl₂) to afford the title compound as light brown solid. ¹H-NMR (DMSO-d₆, 400 MHz): δ = 7.11 (s, br, 1 H), 7.36 (s, br, 1 H), 7.75 (t, J= 8.0 Hz, 1 H), 8.18 (dt, J= 0.8, 8.0 Hz, 1 H), 8.37 (dd, J = 0.8, 7.6 Hz, 1 H), 8.79 (s, 1 H). MS (ES+): m/z 190.18 [MH⁺]. HPLC: t_κ = 1.43 min (ZQ2000, polar_5min).

[804] EXAMPLE 272: 4-{4-[3-(lH-Imidazol-2-yl)-pheny[amino]-7_JH- pyrroloPjS-rfjpyrimidin-β-ylJ-Sjθ-dihydro-lfl-pyridine-l-carboxylic acid tert-butyl ester.

[805] Into a sealed tube were added 4-(4-chloro-7H-pyrrolo[2,3-d]pyrimidin-6-yI)-

3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester (368mg, l.lOmmol), 3-(1H- imidazol-2-yl)-phenylamine (210mg, 1.32mmol), trifluoroacetic acid (847μL, 1 l.Ommol) and 1-butanol (1OmL). The above mixture was heated at 80°C for 24h. After that time, the mixture was concentrated in vacuo, and the residue was dissolved in DMSO for submission for MS-directed purification to obtain brown oil, which was purified again to give the title compound. ¹H NMR (CD₃OD, 400 MHz): 6 = 1.52 (s, 9 H), 2.58 (bis, 2 H), 3.68 (brs, 2 H), 4.14 (brs, 2 H), 6.30 (brs, 1 H), 6.68 (s, 1 H), 7.16 (s, 2 H), 7,45 (t, 1 H, J= 8.0 Hz), 7.57- 7.60 (m, 1 H), 7.76-7.79 (m, 1 H), 8.21 (t, 1 H, J= 1.6 Hz), 9.26 (s, 1 H). MS (ES+): m/z 458.06 (100) [MH⁺]. HPLC: t_R = 2.17 min (ZQ2000, polar_5min). [806] 3-(lH-Imidazol-2-yl)-phenylamine

[807] The compound was obtained from 2-(3 -nitrophenyl)- lH-imidazole following the procedure for dimethyl- {2-[2-(3-nitrophenyl)imidazol-l-yl]ethyl}amine], except that ethanol was used as solvent. ¹H NMR (DMSO-d₆, 400 MHz): δ = 5.14 (s, 2 H), 6.52-6.55 (m, 1 H), 6.96 (s, 1 H), 7.02-7.08 (m, 3 H), 7.16-7.21 (m, 2 H). MS (ES+): m/z 106.19 (100) [MH⁺]. HPLC: /_R = 0.48 min (ZQ2000, polar_5min).

[808] EXAMPLE 273: 4-{4-[3-(lH-Imidazol-2-yl)-phenyIamino]-7H- pyrrolo[2,3-^pyrimidin-6-yl}-3,6-dihydro-2H-pyridine-l-carboxyIic acid tert- butylamide.

[809] Into the solution of 4-{4-[3-(lH-imidazol-2-yl)-phenylamino]-7H- pyrrolo[2,3-rf]pyrimidin-6-yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester (59.4mg, 0.1 lδmmol) in methanol (1.OmL) was added HCl in methanol (9 M, 1.OmL). The above mixture was stirred at rt for 4h. After that time, the mixture was concentrated in vacuo and was then suspended in DMF (2mL). Into the above suspension were added triethylamiαe (159μL, 1.18mmoi) and tert-butyl isocyanate (14.8μL, 0.130mmol). The above mixture was stirred at rt under an atmosphere of N₂ for Ih. After that time, the mixture was concentrated in vacuo to obtain brown oil that was purified by HPLC to yield the title compound. ¹H NMR (CD₃OD, 400 MHz): δ = 1.35 (s, 9 H), 2.55 (brs, 2 H), 3.59 (t, 2 H, J= 4.2 Hz), 4.05 (bra, 2 H), 6.28 (brs, 1 H), 6.65 (s, 1 H), 7.13 (d, 2 H, J= 1.2 Hz), 7.42 (t, 1 H, J= 8.4 Hz), 7.55 (dd, 1 H, J= 0.8 & 7.6 Hz), 7.74 (dd, 1 H, J= 0.8 & 8.0 Hz), 7.75-8.19 (m, 1 H), 8.23 (d, 1 H, J= 1.2 Hz). MS (ES+): m/z 457.12 (100) [MH⁺]. HPLC: t_R = 2.00 min (ZQ2000, polar_5 min). [810] EXAMPLE 274: tert-Butyl 4-(4-{3-t3-(2-dimethylaminoethyl)-3H- imidazol-4-yI]phenylamino}-7jH-pyrrolo[2,3-d]pyrimidin-6-yl)-3,6-dihydro-2i?-pyridine- 1-carboxylate.

[811] 3-[3-(2-Dimemylaminoethyl)-3H-imidazol-4-yl]phenylamine (1 lOmg,

0.478mmol) was added to a solution of tert-butyl 4-(chloro-7H-pyrrolo[2,3-d]pyrimidin-6- yl)-3,6-dihydro-2H-pyridine-l-carboxylate (133mg, 0.398mmol) in 1-butanol (2.OmL). The reaction was stirred at 12O⁰C for 48h. 0.8mL of IN HCl in ether was then added and Hie mixture was stirred further at 12O⁰C for 15h. LC-MS showed the displacement reaction was complete and the BOC group in the desired product was completely removed. Di-tert- butyldicarbonate (347mg, 1.59mmol) and N,N-diisoproρylethylamine (0.347mL, 1.99mmol) were added, and the resulting mixture was stirred at rt for 30min. DMF («1.5mL) was added and the mixture was filtered. The filtrate was purified by HPLC purification to give the title compound. ¹H-NMR (CD₃OD, 400 MHz): δ = 1.50 (s, 9 H), 2.52 (s, 6 H), 2.58 (m, 2 H), 3.04 (t, J= 6.8 Hz, 2 H), 3.67 (m, 2 H), 4.13 (m, 2 H), 4.53 (t, J= 6.8 Hz, 2 H), 6.30 (s, br, 1 H), 6.72 (s, 1 H), 7.18 (s, 1 H), 7.19 (d, J= 7.6 Hz, 1 H), 7.48-7.52 (m, 1 H), 7.72 (dd, J= 2.4, 8.0 Hz, 1 H), 8.06 (s, 1 H), 8.12 (m, 1 H), 8.26 (s, 1 H). MS (ES+): m/z 529 [MH⁺]. HPLC: t_κ = 2.00 min (ZQ2000, polar_5min).

[812] 3- [3-(2-Dimethylaminoethy l)-3iϊ-imidazol-4-yl] phenylamine

[813] A solution of dimethyl-{2-[5-(3-nitroρhenyl)imidazol-l-yl]etliyl}amine

(140mg, 0.54mmol) and 10% Pd/C (80mg) in methanol (8mL) was hydrogenated under 1 atm hydrogen pressure for 5h. The reaction mixture was filtered through a Celite pad. The filtrate was concentrated to dryness to afford the desired amine, which was used directly in the next step without purification. ¹H-NMR (CDsOD, 400 MHz): δ = 2.15 (s, 6 H), 2.49 (t, J= 6.8 Hz, 2 H), 4.18 (t, J= 7.2 Hz, 2 H), 6.69-6.77 (m, 3 H), 6.91 (d, J= 1.2 Hz, 1 H), 7.18 (dt, J= 1.2, 7.6 Hz, 1 H), 7.44 (d, J= 0.8 Hz, 1 H). MS (ES+): m/z 231.29 [MH⁺]. HPLC: *_R = 0.39 min (ZQ2000, polar_5min). [814] Dimethyl-{2-[5-(3-nitrophenyl)imidazol-l-yl]ethyI}amine

[815] A stirred mixture of 3-[2-(3-nitrophenyl)-2-oxoethyl]-3H-quinazoBn-4-one

(2.0Og, 6.47mmol), NiV-dimethyl-l ,2-ethanediamine (2.28g, 25.9mrnol), sadp- toluenesulfonic acid (2.23 g, 12.9mmol) in xylenes (15OmL) was refiuxed for 48h. After cooling to rt, water (2OmL) and sat. NaHCO₃ (aq) (15mL) were added. Layers were separated, and the aqueous phase was extracted with EtOAc (3 x 5OmL). The combined organic phases were dried over MgSO₄, filtered, concentrated, and purified by silica gel chromatography (8% MeOH in CH₂Cl₂) to afford the desired product. ¹H-NMR (CD₃OD, 400 MHz): δ = 2.15 (s, 6 H), 2.54 (t, J= 7.2 Hz, 2 H), 4.22 (t, J= 6.8 Hz, 2 H), 7.15 (d, J= 1.2 Hz, 1 H)₅ 7.74 (t, J= 8.0 Hz, 1 H), 7.89 (dt, J=2.4, 7.6 Hz, 1 H), 7.90 (s, 1 H), 8.24-8.26 (m, 1 H), 8.30 (s, 1 H). MS (ES+): m/z 261.24 [MH⁺]. HPLC: t_R = 0.49 and 0.71 min (ZQ2000, polar__5min). [816] 3-[2-(3-NitrophenyI)-2-oxoethyI]-3iJ-quinazolin-4-one

[817] To a solution of 4(3H)-quinazolinone (2.19g, 15.0 mol) in anhydrous DMF

(1OmL) was added NaH (60% dispersion in mineral oil, 0.719g, 18.0mmol) in two portions with caution. The mixture was stirred at rt for 30min. 3-Nitrophenacyl bromide (4.39g, lδ.Ommol) was added and the resulting suspension was stirred at rt for 16h. Solvent was removed under reduced pressure. To the residue were added water (1OmL) and 4 N HCl (aq) to adjust the pH to «6. The solid material was collected by filtration, washed with water (2OmL) and dichloromethane (3x20mL) to afford the title compound as a white powder. ¹H- NIvIR (CD₃OD, 400 MHz): δ = 5.70 (d, J= 10.0 Hz, 2 H), 7.60 (d, J= 7.2 Hz, 1 H), 7.76 (d, J = 8.4 Hz, 1 H), 7.86-7.91 (m, 2 H), 8.25 (d, J= 8.0 Hz, 1 H), 8.30 (s, 1 H), 8.51-8.58 (m, 2 H), 8.90 (t, J= 1.2 Hz, 1 H). MS (ES+): _m/z 310.06 [MH⁺]. HPLC: fe = 2.90 min (ZQ2000, polar_5min).

[818] EXAMPLE 275: tert-Butyl 4-{4-[3-(lH-benzimidazol-2-yI)phenyI- amino]-7H-pyrroIo[2,3-<flpyrimidin-6-yl}-3,6-dihydro-2iy-pyridine-l-carboxyIate.

[819] The title compound was obtained following the General method for the reaction of amines with tert-butyl 4-(4-chloro-7H-pyrrolo[2,3-d]pyrimidin-6-yl)-3,6- dihydropyridine-l(2H)-carboxylate, using 3-(lH-Benzimidazol-2-yl)-phenylamine. ¹H-NMR (CD₃OD, 400 MHz): δ = 1.50 (s, 9 H), 2.58 (m, 2 H), 3.67 (m, 2 H), 4.13 (m, 2 H), 6.31 (s, br, I H), 6.72 (s, 1 H), 6.26-6.30 (m, 2 H), 7.54 (t, J= 8.0 Hz, 1 H), 7.63 (m, 2 H), 7.79 (dt, J= 0.8, 8.4 Hz, 1 H), 7.88 (dt,J= 0.8, 8.0 Hz, 1 H), 8.29 (s, 1 H), 8.50 (m, 1 H). MS (ES+): m/z 508.03 [MH⁺]. HPLC: *_R = 2.72 min (ZQ2000, polar_5min).

[820] EXAMPLE 276: tert-Butyl 4-{4-[3-(l-methylpiperidin-4-yI)phenyl- amino]-7H-pyrrolo[2,3-rf]pyriinidin-6-yl}-3,6-dihydro-2JΪ-pyridine-l-carboxylate.

[821] The title compound was obtained following the General method for the reaction of amines with tert-butyl 4-(4-chloro~7H-ρyrrolo[2,3-<^pyrimidin-6-yl)-3,6- dihydropyridine-l(2H)-carboxylate, using 3-(l-methylpiperidin-4-yl)phenylamine. ¹H-NMR (CD₃OD, 400 MHz): δ = 1.49 (s, 9 H), 1.72-1.85 (m, 2 H), 1.93-1.97 (m, 2 H), 2.56 (m, 2 H), 2.74 (s, 3 H), 2.81 (m, 1 H), 3.21 (t, J= 12.8 Hz, 2 H), 3.64 (m, 2 H), 4.11 (m, 2 H), 4.86 (d, J = 13.2 Hz, 2 H), 6.25 (s, br, 1 H), 6.48 (dt, J = 2.4, 8.0 Hz, 1 H), 6.53-6.59 (m, 3 H), 7.05 (t, J = 7.6 Hz, 1 H), 8.12 (s, 1 H). MS (ES+): m/z 489.14 [MH⁺]. HPLC: t_κ = 2.50 min (ZQ2000, polar_5min). [822] 3-(l-MethyIpiperidin-4-yI)phenylamine

[823] A dried flask was charged with tert-hutyl 4-(3 -aminophenyl)piρeridine- 1 - carboxylate (0.553g, 2.00mmol). Lithium aluminium hydride (IM in THF, 1OmL, lO.Ommol) was added slowly through a syringe under N₂. The resulting mixture was stirred overnight at it Water (0.5mL) was cautiously added to quench the reaction. The resulting mixture was filtered. The filtrate was concentrated to dryness to give the title compound as a white solid, which was used without further purification in the next step. ¹H-NMR (CDCl₃, 400 MHz): δ = 1.80-1.85 (m, 2 H), 2.04 (dt, J= 4.0, 11.6 Hz, 2 H), 2.33 (s, 3 H), 2.40 (m, 1 H), 2.98 (m, 2 H), 3.64 (s, br, 2 H), 6.54-6.59 (m, 2 H), 6.66 (d, J= 7.6 Hz, 1 H), 7.10 (t, J= 7.6 Hz, 1 H). MS (ES+): m/z 191.26 [MH⁺]. HPLC: & = 0.49 min (ZQ2000, polar_5rnin). [824] EXAMPLE 277: fert-Butyl 4-[4-(3-piperidin-4-yIphenylamino)-7J3- pyrrolo[2,3-//)pyrimidiπ-6-yl]-3,6-dihydro-2Zf-pyridine-l-carboxyIate.

[825] The title compound was also isolated from the above reaction mixture. ¹H-

NMR (CD₃OD, 400 MHz): 8 = 1.50 (s, 9 H), 1.71-1.80 (m, 2 H), 1.93-1.96 (m, 2 H), 2.56 (m, 2 H), 2.75-2.81 (m, 1 H), 3.21 (dt, J= 2.8, 13.2 Hz, 2 H), 3.64 (m, 2 H), 4.11 (m, 2 H), 4.86 (d, J= 13.2 Hz, 2 H), 6.26 (s, br, 1 H), 6.56-6.64 (m, 4 H), 7.02 (t, J= 7.6 Hz, 1 H), 8.12 (s, 1 H). MS (ES+): m/z 475.12 [MH⁺]. HPLC: /_R = 2.43 min (ZQ2000, polar_5min). [826] EXAMPLE 278: 4-{4-[4-F!uoro-3-(l-methylpiperidin-4-yl)-phenyl- aminoJ^ff-pyrrolo^_jS-rflpyriniidin-ό-ylJ-S_jό-dihydro^H-pyridine-l-carboxylic acid tert-buty\ ester.

[827] A mixture of 4-(4-chloro-7H-pyrrolo[2,3 -φyrimidin-6-yl)-3 ,6-dihydro-2H- pyridine-1-carboxylic acid tert-bvtiyl ester (167mg, 0.500mmol), 4-fluoro-3-(l- methylpiperidin-4-yl)-phenylamine (149mg, O.όOOmmol), N^V-dimethylformamide (3mL), and trifluoroacetic acid (385μL, 5.18mmol) in a sealed tube was heated at 100⁰C for 15h. The mixture was concentrated in vacuo, charged with sodium bicarbonate (504mg, ό.OOmmol), di-fert-butyldicarbonate (120mg, 0.550mmol), and N,N-dimethylformarnide (2mL), and stirred at rt under N₂ for 24h. After that time, the mixture was filtered, and the filtrate was concentrated in vacuo to obtain a brown oil, which was dissolved in EtOAc (3OmL) and washed with water (3 x 2OmL). The organic phase was concentrated in vacuo to obtain a light-brown oil that was purified by HPLC to give the title compound. ¹H NMR (CD₃OD, 400 MHz): δ = 1.51 (s, 9 H), 1.87 (brs, 4 H), 2.13-2.20 (m, 2 H), 2.32 (s, 3 H), 2.54 (brs, 2 H), 2.83-2.91 (m, 1 H), 2.99-3.01 (m, 2 H), 3.65 (brs, 2 H), 4.12 (brs, 2 H), 6.27 (brs, 1 H), 6.56 (s, 1 H), 7.03 (t, 1 H, J= 8.8 Hz), 7.57-7.60 (m, 2 H), 8.19 (s, 1 H). MS (ES+): m/z 507.17 (75) [MH⁺]. HPLC: t_R = 2.16 min (ZQ2000, polar_5min). [828] 4-FIuøro-3-(l-methylpiperidin-4-yl)-phenylamine

[829] Pd/C (10% w/w, 50% water, 77mg) was added to the solution of 3-fluoro-4-

(l-methyl-l,2,3,6-tetrahydropyridin-4-yl)-phenylamine (386mg, 1.57mmol) in methanol (1OmL). The above mixture was degassed and then the H₂ balloon was applied. The mixtrure was stirred at rt under an atmosphere Of H₂ overnight. Additional Pd/C (10%w/w, 50% water, 77mg) was added, and stirring was continued overnight. The mixture was filtered and concentrated in vacuo to give the title compound as brown oil that was used for the next reaction without further purification. ¹H NMR

400 MHz): δ = 1.55 -1.64 (m, 4 H), 2.05 - 2.11 (m, 2 H), 2.22 (s, 3 H), 2.54 - 2.62 (m, 1 H), 2.88 - 2.97 (m, 2 H), 6.29 - 6.33 (m, 1 H), 6.38 - 6.41 (m, 1 H), 6.69 - 6.73 (m, 1 H). MS (ES+): m/z 209.29 (100) [MH⁺]. HPLC: t_κ = 0.46 min (ZQ2000, polar_5 min). [830] 4-Fluoro-3-(l-methyl-l,2,3,6-tetrahydropyridin-4-yl)-phenylamine

[831] A dried flask was charged with 4-(2-fluoro-5-nitrophenyl)-3,6-dihydro-2H- pyridine-1-carboxylic acid tert-butyl ester (645mg, 2.00mmol) and THF (1OmL). Lithium aluminium hydride (IM in THF, 2OmL, 20.0mmol) was added slowly through a syringe under N₂ (the reaction was very exothermic). The resulting mixture was stirred for 16h at rt. Water was cautiously added to quench the reaction. The resulting mixture was filtered, and the filtrate was concentrated to dryness to give the title compound as a brown oil. ¹H NMR (DMSO-^₅, 400 MHz): δ = 2.14 (s, 3 H), 2.38 - 2.44 (m, 2 H), 2.89 - 2.90 (m, 2 H), 3.22 (brs, 2 H), 5.95 (brs, 1 H), 7.24 - 7.29 (m, 1 H), 7.67- 7.73 (m, 2 H), 8.16 (s, 1 H). MS (ES+): m/z 206.26 (100) [MH⁺]. HPLC: t_R = 1.68 min (ZQ2000, polar_5 min). [832] 4-(2-fluoro-5-nitrophenyl)-3,6-dihydro-2H-pyridine-l-carboxyIic acid tert-butyl ester

[833] Into a 1 -neck round-bottom flask were added 2-bromo-l -fluoro-4- nitrobenzene (1760mg, δ.OOOmmol), potassium carbonate (2210mg, lβ.OOmmol), 4-(4,4,5,5- tetramethyl[ 1 ,3,2]dioxaborolan-2-yl)-3 ,6-dihydro-2H-pyridine-l -carboxylic acid tert-butyl ester (2720mg, 8.800mmol), water (8mL) and 1,4-dioxane (32mL). The flask was degassed and filled with N₂ for 3 times, and then [l,l'-bis(diphenylphosphino)ferrocene]- dichloroρalladium(II) complex with CH₂Cl₂ (1:1) (330.0mg, 0.4000mmol) was added. The mixture was degassed and filled with N₂ for 3 times again and was then heated at 100°C for 16h. After that time, the mixture was concentrated in vacuo and was then purified by silica gel (240 g) eluting with 180OmL of 5%, 100OmL of 10%, 100OmL of 15% and 100OmL of 20% EtOAc/hexane to obtain the title compound as a colorless oil. ¹H NMR (DMSO-d₆, 400 MHz): δ = 1.49 (s, 9 H), 2.52 - 2.55 (m, 2 H), 3.60 (t, 2 H, J= 5.6 Hz), 4.09 (brs, 2 H), 6.21 (bis, 1 H), 7.55 - 7.60 (m, 1 H), 8.21 - 8.29 (m, 2 H). MS (ES+): m/z 223.22 (100) [MH⁺ - Boc]. HPLC: t_κ = 3.83 min (ZQ2000, polar_5min).

[834] EXAMPLE 279: 4-[4-(3-Methyl-3H-benzimidazol-5-yIamino)-7H- pyrrolo[2,3-rf]pyriniidra-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester.

[835] A mixture of 4-(4-chloro-7H-pyrrolo[2,3-rf]pyrimidin-6-yl)-3,6-dihydro-2H- pyridine-1 -carboxylic acid tert-butyl ester (134mg, 0.400mmol) and 3-methyl-3H- benzoimidazol-5-ylamine (70.6mg, 0.480mmol) in «-BuOΗ (3mL) in a sealed tube was heated at 12O⁰C for 17h and concentrated in vacuo to obtain a brown solid that was purified using the mass-directed purification system to yield the title compound as beige solid. ¹H NMR (CD₃OD, 400 MHz): δ = 1.52 (s, 9 H), 2.57 (brs, 2 H), 3.68 (brs, 2 H), 3.93 (s, 3 H), 4.12 (brs, 2 H), 6.31 (brs, 1 H), 6.65 (brs, 1 H), 7.46 (dd, 1 H, J= 2.0 & 8.4 Hz), 7.66 (d, 1 H, J= 8.8 Hz), 8.14 - 8.15 (m, 2 H), 8.23 (s, 1 H), 8.24 (brs, 1 H). MS (ES+): m/z 464.12 (100) [MH⁺]. HPLC: fe = 2.18 min (ZQ2000, polar_5 min). [836] 3-Methyl-3H-benzimidazol-5-ylamine

[837] Pd/C (17mg, 10%, with 50% water) was added into the suspension of 1- methyl-6-nitro-lH-l,3-benzimidazole (85.0mg, 0.480mmol) in ethanol (3mL). The mixture was degassed and filled with H₂. The mixture was stirred at rt under balloon pressure for 16h. After that time, the mixture was filtered and concentrated in vacuo to obtain the title compound as pink crystals. ¹H NMR (CD₃OD, 400 MHz); δ = 3.67 (s, 3 H), 6.69 - 6.73 (m, 2 H), 7.33 (dd, 1 H, /= 0.4 & 8.8 Hz), 7.77 (s, 1 H). MS (ES+): m/z 148.16 (100) [MH⁺]. HPLC: t_R = 0.43 min (ZQ2000, polar_5 min).

[838] EXAMPLE 280: 4-[4-(3-Methyl-3H-benzimidazol-5-ylamino)-7H- pyrroloPβ-rflpyrimidin-δ-ylJ-Sjό-dihydro-IH-pyridine-l-carboxylic acid teri'- butylamide.

[839] Into the solution of 4-{4-[3-(lH-imidazol-2-yl)-phenylamino]-7H- pyrrolo[2,3-</Jpyrimidin-6-yl}-3,6-diliydro-2H-pyridine-l-carboxylic acid tert-butyl ester (EXAMPLE 279) (59.4mg, 0.1 lδmmol) in methanol (1.OmL) was added HCl in methanol (9M, 1.OmL). The above mixture was stirred at rt for 4h. After that time, the mixture was concentrated in vacuo and suspended in DMF (2mL). Into the above suspension were added triethylamine (159μL, l.lδmmol) and tert-butyl isocyanate (14.8μL, 0.130mmol). The above mixture was stirred at rt under of N₂ for Ih and concentrated in vacuo to obtain a brown oil that was purified using the mass-directed purification system to yield the title compound. ¹H NMR (CD₃OD, 400 MHz): δ = 1.37 (s, 9 H), 2.56 (brs, 2 H), 3.61 (t, 2 H, J= 4.8 Hz), 3.90 (s, 3 H), 4.07 (brs, 2 H), 5.69 (s, 1 H), 6.29 (brs, 1 H), 6.62 (s, 1 H), 7.43 (dd, 1 H, J= 2.0 & 8.8 Hz), 7.63 (d, 1 H, /= 8.8 Hz), 8.08 (s, 1 H), 8.11 (d, 1 H, J= 2.0 Hz), 8.22 (s, 1 H). MS (ES+): m/z 445.11 (100) [MH⁺]. HPLC: /_R = 2.00 min (ZQ2000, polar_5 min). [840] EXAMPLE 281: ter^ButyI 4-[4-(benzothiazol-5-yIamino)-7H- pyrrolo[2,3-^pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxamide.

[841] A solution of benzothiazol-5-yl-[6-(l,2,3,6-tetrahydropyridin-4-yl)-7H- pyrrolo[2,3-d]pyriimdin-4-yl]amine trihydrochloride (23mg, 0.050mmol) and NN- diisopropylethylamine (0.07mL, 0.402mmol) in DMF (2mL) was stirred at rt for 30min. tert- Butyl isocyanate (0.012mL, 0. lOinmol) was added dropwise through a syringe. The resulting mixture was stirred for 1.5h at rt. MeOH (0.5mL) was added to quench the reaction. The whole mixture was filtered and purified by HPLC to afford the desired product. ¹H-NMR (DMSO-d₆, 400 MHz): δ = 1.28 (s, 9 H), 2.48 (m, 2 H), 3.53 (m, 2 H), 4.01 (m, 2 H), 5.79 (s, 1 H), 6.43 (s, br, 1 H), 6.84 (s, 1 H), 7.92 (d, /= 8.4 Hz, 1 H), 8.08 (d, /= 8.8 Hz, 1 H), 8.35 (d, J= 1.2 Hz, 1 H), 8.88 (s, 1 H), 9.37 (d, J= 1.2 Hz, 1 H), 9.56 (s, 1 H), 11.99 (s, 1 H). MS (ES+): m/z 448.08 [MH⁺]. HPLC: t_R = 2.60 min (ZQ2000, polar_5min). [842] BenzothiazoI-5-yI-[6-(l,2,3,6-tetrahydropyridin-4-yl)-7#-pyrrolo[2,3- d]pyrimidin-4-yl] amine trihydrochloride

[843] To a suspension of tot-butyl 4-[4-(benzothiazol-5-ylamino)-7H-pyrrolo[2,3- rf]pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylate (28.3mg, 0.063mmol) in MeOH (3mL) was added 4 N HCl (aq) (3mL). The mixture was stirred at 6O⁰C for 8h. Solvents were removed under reduced pressure to afford the title compound as yellow solid, which was used directly in the next step without purification. ¹H-NMR (DMSOd₆, 400 MHz): δ = 2.70 (m, 2 H), 3.83 (m, 2 H), 6.45 (s, 1 H), 6.99 (s, 1 H), 7.82 (d, J= 8.4 Hz, 1 H), 8.19 (d, J= 8.8 Hz, 1 H), 8.36 (s, 1 H), 8.68 (s, 1 H), 9.07 (s, 1 H), 9.44 (s, 1 H), 10.32 (s, br, 1 H), 12.51 (s, 1 H). MS (ES+): m/z 349.06 [MH⁺]. HPLC: /_R = 1.73 min (ZQ2000, polar_5min). [844] EXAMPLE 282: fert-Butyl 4-[4-(benzothiazol-5-yIamino)-7H- pyrrolo[2,3-rf]pyrimidin-6-yI]-3,6-dihydro-2H-pyridine-l-carboxylate.

[845] The title compound was obtained following the General method for the reaction of amines with tot-butyl 4-(4-chloro-7H-pyrrolo[2,3-J]pyrimidin-6-yl)-3,6- dihydropyridine-l(2H)-carboxylate, using benzothiazol-5-ylamine. ¹H-NMR (CD₃OD, 400 MHz): δ = 1.50 (s, 9 H), 2.58 (m, 2 H), 3.67 (m, 2 H), 4.14 (m, 2 H), 6.31 (s, br, 1 H), 6.73 (s, 1 H), 7.85 (dd, J = 2.4, 8.8 Hz, 1 H), 8.01 (d, J= 8.8 Hz, 1 H), 8.27 (s, 1 H), 8.67 (d, J= 1.6 Hz, 1 H), 9.24 (s, 1 H). MS (ES+): m/z 449.02 [MH⁺]. HPLC: t_R = 3.01 min (ZQ2000, polar_5min).

[846] EXAMPLE 283: 4-[4-(3-MethyI-lH-indazoI-5-yIamino)-7#-pyrroIo[2,3- d]pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester.

[847] A mixture of 4-(4-chloro-7#-ρyrrolo[2,3-φyrimdm-6-yl)-3 ,6-dihydro-2H- pyridine-1-carboxylic acid tert-buτyl ester (50.1mg, 0.150mmol) and 3-methyl-lH-indazol-5- ylamine (25.0mg, 0.170mmol) in /PrOH (2.5mL) in a sealed tube was heated to 9O⁰C (bath temp.) for 16h. The solvent was evaporated, water/NaHCO₃ solution was added, the mixture was extracted with CH₂Cl₂ (3x30mL), and the combined extracts were washed with brine and dried over MgSO₄. The extracts were filtered through a pad of silica gel, washing with 5% MeOH in CH₂Cl₂ until no more product eluted as indicated by TLC. Concentration in vacuo gave a light brown solid. The solid was triturated with MeOH, filtered, washed with more MeOH, and dried in vacuo overnight. One obtained the title compound as white solid, mp. 245-25O⁰C (decomp.). ¹H NMR (DMSO-J₆, 400 MHz): δ = 1.43 (s, 9H), 2.42-2.50 (brs, 2H), 2.47 (s, 3H), 3.53-3.59 (rri_c, 2H), 3.99-4.08 (m, 2H), 6.38 (brs, IH), 6.73 (brs, IH), 7.43 (d, J= 8.8 Hz, IH), 7.69 (dd, J= 1.6, 8.8 Hz, IH), 8.15 (s, IH), 8.23 (s, IH), 9.32 (s, IH), 11.88 (brs, IH), 12.54 (s, IH). MS (ES+): m/z 446.0 (100) [MH⁺]. HPLC: t_κ = 2.4 min (ZQ2000, polar__5min).

[848] EXAMPLE 284: l-{4-[4-(3-Methyl-lH-indazol-5-ylamino)-7H- pyrrolo[2,3-«?]pyrimidin-6-yI]-3,6-dihydro-2J?-pyridin-l-yI}-3-piρeridin-l-yI-propan-l- one.

[849] Into the suspension of (3-methyl-lH-indazol-5-yl)-[6-(l ,2,3,6-tetrahydro pyridin4-yl)-7H-pyrτolo[2,3-d]pyrimidin-4-yl]-amine tris-hydrochloride (122mg, 0.19OnTmOi), 1-piperidinepropanoic acid (48.4mg, 0.305mmol),N-(3-dimethylaminopropyl)- N'-ethylcarbodiimide hydrochloride (EDC-ΗC1) (76.7mg, 0.400mmol) and 1 -hydroxy benzotriazole (HOBt-H₂O) (30.6mg, 0.200mmol) in DMF (4.5mL) was added N^/- diisopropylethylamine (167μL, 0.952mmol) under N₂ at rt. The reaction mixture, which became a clear wine-red solution, was stirred at rt for 18h. After that time, the reaction mixture was treated with water / saturated NaHCO₃ (5mL/5mL) and extracted with EtOAc (4 x 2OmL). The combined extracts were washed with water (2 x 2OmL) and brine (2OmL), dried over MgSO₄, filtered and concentrated in vacuo to obtain a light-brown oil that was purified using the mass-directed purification system to yield the title compound as yellow oil. ¹H NMR (CD₃OD, 400 MHz): δ = 1.69 (brs, 2 H), 1.88 (brs, 4 H), 2.57 (s, 3 H), 2.66 (brs, 2 H), 2.95 - 3.03 (m, 2 H), 3.32 (brs, 4 H), 3.41 (t, 2 H, J= 6.0 Hz), 3.76 (t, 1 H, J= 5.4 Hz), 3.85 (t, 1 H, J= 5.6 Hz)₅4.28 (brs, 2 H), 6.30 (d, 1 H, J= 2.8 Hz), 6.51 - 6.55 (m, 1 H), 7.49 (d, 1 H, J= 8.4 Hz), 7.55 - 7.59 (m, 1 H), 7.98 - 8.00 (m, 1 H), 8.19 (s, 1 H), 8.42 (s 1 H). MS (ES+): m/z 485.00 (70) [MH⁺]. HPLC: t_κ = 1.70 min (ZQ2000, ρolar_5 min). [850] EXAMPLE 285: (3-Methyl-li3-indazoI-5-yl)-[6-(l,2,3,6-tetrahydro- pyridin-4-yl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl] -amine tris-hydrochloride.

[851] To a suspension of 4-[4-(3-methyl-lH-indazol-5-ylamino)-7H-pyrrolo[2,3- rf]pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester (488mg, l.lOmmol) in MeOH (1OmL) was added hydrogen chloride (9M in MeOH, 2.15mL, 19.4mmol), the mixture was stirred at rt for 3h and concentrated in vacuo. The residue was triturated with Et₂O and dried in vacuo to give the title compound. MS (ES+): m/z 347.12 (10) [MH⁺]. HPLC: *_R(polar-5 mins) = 1.52 min (ZQ2000, polar_5 min). A purified sample was made by Gilson HPLC to record the ¹H NMR spectrum. ¹H NMR (DMSO-ck, 400 MHz): δ = 2.34 (s, 3 H), 2.47 (brs, 2 H), 3.12 (brs, 2 H), 3.60 (brs, 2 H), 6.29 (s, 1 H), 6.92 (s, 1 H), 7.07 (s, 1 H), 7.19 (s, 1 H), 7.25 (d, 1 H, J= 8.4 Hz), 7.40 (d, 1 H, J= 8.4 Hz), 7.75 (s, 1 H), 8.06 (s, 1 H), 9.27 (brs, 1 H), 12.73 (brs 1 H).

[852] EXAMPLE 286: 3-DimethyIamino-l-4-[4-(3-methyl-lH-indazol-5-yl- amino)-7H-pyrroIo[2,3-^pyrimidin-6-yI]-3,6-dihydro-2#-pyridin-l-yIpropan-l-one.

[853] The title compound (yellow solid) was prepared following the procedure for

1 - {4-[4-(3 -methyl-lH-indazol-5-ylamino)-7H-pyrrolo[2,3 - J]pyrrmidin-6-yl] -3 ,6-dihydro~2H- pyridin-l-yl}-3-piperidin-l-yl-propan-l-one, using 3-dimethylaminopropionic acid. ¹H NMR (400 MHz, MeOH-^): δ = 2.21 & 2.22 (s, rotamers, 6H), 2.47 (s, 4H), 2.49-2.57 (m, 2H), 2.60 (s, 3H), 3.68 & 3.72 (t, J= 5.6 Hz, rotamers, 2H), 4.16 & 4.20 (s, rotamers, 2H), 6.20 (s, IH), 6.40 & 6.45 (s, rotamers, IH), 7.38 (d, J= 8.8 Hz, IH), 7.47 (d, J= 8.8 Hz, IH), 7.88 (d, J= 4.0 Hz, IH), 8.08 (s, IH). MS (ES+): m/z 445.03 (50) [MH⁺]. HPLC: t_κ = 1.63 min (ZQ2000, polar_5min).

[854] EXAMPLE 287: 3-Imidazol-l-yl-l-{4-[4-(3-methyl-lH-indazol-5- ylamino)-7H-pyrrolo[2,3-rf]pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yl}-propan-l-one.

[855] /3-Bromopropionic acid (29.1mg, 0.190mmol), lH-imidazole (19.4mg,

0.286mmol), potassium carbonate (160mg, l,16mmol) and DMF (3mL) was combined together and stirred at rt for 2Oh. After that time, (3-methyl-lH-indazoI-5-yl)-[6-(l ,2,3,6- tetoahydropyridin^-yl)-7H-pyiτolo[2,3-^pyrimidin-4-yl]-arnine hydrogen chloride tri-salt (122mg, 0.190mmol), N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride (76.7mg, 0.400mmol), and 1-hydroxybenzotriazole (27.0mg, 0.200mmol) was added into the above reaction mixture and was stirred at rt under an atmosphere of N₂ for 24h. After that time, the mixture was filtered and the filtrate was concentrated in vacuo. The residue was dissolved in DMSO for submission to MS-directed purification to obtain the title compound as beige oil. ¹H NMR (DMSO-^, 400 MHz): δ = 2.54-2.56 (m, 2 H), 2.59 (s, 3 H), 2.97- 3.07 (m, 2 H), 3.73 (t, 1 H, J= 5.2 Hz), 3.80 (t, 1 H, J= 5.6 Hz), 4.25 (brs, 2 H), 4.30^.33 (m, 2 H), 6.48 (d, 1 H, J= 4.0 Hz), 6.80 (d, 1 H, J= 18.8 Hz), 6.94 (d, 1 H, J= 0.8 Hz), 7.28- 7.30 (m, 1 H), 7.52 (d, 1 H, J= 8.8 Hz), 7.73 (t, 1 H, J= 0.8 Hz), 7.76-7.80 (m, 1 H), 8.23 (dd, 1 H, J= 1.2 & 6.8 Hz), 8.32 (d, 1 H, J= 2.0 Hz), 9.40 (s, 1 H), 12.01 (brs, 1 H), 12.56 (brs, 1 H). MS (ES+): m/z 468.11 (10) [MH⁺]. HPLC: /_R = 1.62 min (ZQ2000, polar_5 min). [856] EXAMPLE 288: 4-[4-(3-Methoxy-lff-indazol-5-ylamino)-7i3^r- pyrrolo[2,3-^pyrimidin-6-yl]-3,6-dihydro-2jH-pyridine-l-carboxylic acid tert-butyl ester.

[857] A mixture of 4-(4-chloro-7H-pyrrolo[2,3-φyriirήdin-6-yl)-3 ,6-dihydro-2H- pyridine-1-carboxylic acid tert-butyl ester (48.2mg, 0.144mmol) and 5-amino-3- methoxyindazole-1-carboxylic acid tert-butyl ester (40.4mg, 0.153mmol) in isopropyl alcohol (3.OmL) in a sealed tube was heated to 85⁰C (bath temp.) for 16h. LC/MS at that time showed the product (minor), indazole-Boc-product (major), de-Boc product (minor), and both starting materials. The bath temperature was increased to 9O⁰C, and heating was continued for 2d. After reaching rt, di-ter/-butyldicarbonate (15mg, 0.069mmol) and NN- diisopropylethylamine (0.ImL, 0.6mmol) were added to the reaction mixture, and the now clear solution was stirred at rt for 2h. LC/MS at that time indicated complete conversion of the de-Boc product to the product. 14.8 M of ammonia in Water (2.OmL) was added, and the mixture was stirred at rt overnight and heated to 90⁰C for 5h. Sodium hydroxide (6.5mg, 0. lόmmol) was added, and heating was continued overnight. Water and sat. NH₄Cl solution were added, the mixture was extracted with CH₂Cl₂ (10OmL) and CH₂Cl₂:Me0H 10:1 (5OmL), and the combined organic layers were dried over MgSO₄. The organic solution was filtered through a plug of silica gel (∞ 1 " in a 6OmL glass frit), which was further washed with 5% MeOH in CH₂Cl₂ until the entire product was eluted. The solution containing the product was concentrated and dried overnight in vacuo. The solid from the aqueous phase was filtered off, washed with water, and dried in vacuo overnight. From the precipitate of the aqueous phase, one obtained the title compound as light brown solid. From the silica gel plug filtration, one obtained a light brown solid that was further purified by MDP to give the title compound as off-white solid. ¹H NMR (DMSO-J₆, 400 MHz): δ = 1.44 (s, 9H), 2.42-2.50 (brs, 2H), 3.52-3.60 (m,, 2H), 4.00 (s, 3H), 3.98-4.07 (m, 2H), 6.38 (brs, IH), 6.75 (brs, IH), 7.34 (d,/= 8.8 Hz, IH), 7.62 (dd, J= 2.0, 8.8 Hz, IH), 8.25 (s, IH), 8.26 (s, IH), 9.29 (s, IH), 11.78 (s, IH), 11.90 (s, IH). MS (ES+): m/z 462.0 (100) [MH⁺]. HPLC: t_R = 2.5 min (ZQ2000, polar_5min). J858] S-Amino-S-methoxyindazoIe-l-carboxylic acid tert-buty\ ester

[859] S-Methoxy-S-nitroindazole-l-carboxylic acid ferZ-butyl ester (0.33g,

1.1 lmmol) and palladium (10% wt) on carbon (0.24g, 20% wt) were dissolved in EtOAc (25mL). The flask was evacuated and filled with N₂ (x5), then evacuated and filled with hydrogen (x 10) and left over a weekend. The mixture was filtered over celite and the solvents removed in vacuo. Purification by column chromatography on silica gel (Jones, 20 g) loading in DCM and eluting in 5:1 Hexanes:EtOAc stepwise to 7:3 Hexanes:EtOAc yielded the title compound as a white powder. ¹H NMR (400 MHz, CDCl₃): δ = 1.69 (s, 9H), 3.73 (brs, 2H), 4.15 (s, 3H), 6.85 (d, J= 2.0 Hz, IH), 6.91 (dd, J= 8.8, 2.4 Hz, IH), 7.74 (brs, IH). MS (ES+): m/z 164.3 (65) [MH⁺] (fragment ion, loss of Boc group). [860] S-Methoxy-S-nitroindazole-l-carboxylic acid tert-butyl ester

[861] To a pre-dried flask were added 5-nitro-3-oxo-2,3-dihydroindazole- 1 - carboxylic acid ter/-butyl ester (0.65g, 2.33mmol), triphenylphosphine (0.92g, 3.50mmol), methanol (115μL, 2.80mmol) and anhydrous THF (1OmL). The flask was evacuated and purged with N₂ then cooled to 0⁰C and diisopropylazodicarboxylate (690/zL, 3.50mmol) added dropwise over 5min. The mixture was stirred at rt overnight then diluted with EtOAc and partitioned over water. The organic layer was washed with brine, dried (MgSO₄), filtered and concentrated. Purification by column chromatography on silica gel (Jones, 5Og) loading and eluting in DCM revealed the title compound as a white powder. ¹H NMR (400 MHz, CDCl₃): δ = 1.68 (s, 9H), 4.21 (s, 3H), 8.10 (d, J= 8.8 Hz, IH), 8.39 (dd, J= 9.2 Hz, 2.4 Hz, IH), 8.61 (d, J= 2.0 Hz, IH). MS (ES+): m/z 294.3 (20) [MH⁺]. The N-alkylation product methyl-5-nitro-3-oxo-2,3-dihydroindazole-l-carboxylic acid tert-butyl ester was also isolated. ¹H ΝMR (400 MHz, CDCl₃): δ = 1.68 (s, 9H), 3.69 (s, 3H), 8.02 (d, J= 9.2 Hz, IH), 8.48 (dd, J= 9.2, 2.4 Hz, IH), 8.77 (d, J= 2.0 Hz, IH). [862] S-Νitro-S-oxo^S-dihydroindazole-l-carboxylic acid tert-butyl ester

[863] A suspension of 5-nitro-l,2-dihydroindazol-3-one (2.0Og, 11.2mmol) and di- fert-butyl-dicarbonate (3.17g, 14.5mmol) was stirred in anhydrous DCM at 0 ⁰C and DMAP (0.34g, 2.79mmol) was added. The mixture turned deep red in color and after 10 minutes a precipitate had formed. This precipitate was filtered and washed with DCM, then dried in vacuo to give the desired product as an off-white powder. ¹H ΝMR (400 MHz, DMSOd₆): δ = 1.63 (s, 9H), 8.16 (d, J= 9.2 Hz, IH), 8.42 (dd, J= 9.2, 2.0 Hz, IH), 8.61 (d, J= 2.4 Hz, IH), 12.63 (bra, IH). MS (ES+): m/z 559.3 (100) [MH⁺] (dimer).

[864] EXAMPLE 289: 4-[4-(l-MethyI-l#-indazol~5-yIamino)-7#-pyrrolo[2,3- rfJpyrimidin-6-yI]-3,6-dihydro-2H-pyridine-l-carboxyIic acid tert-butyl ester.

[865] A suspension of 4-(4-chloro-7H-pyrrolo[2,3-rf]pyrimidin-6-yl)-3,6-dihydro-

2H-pyridine-l-carboxylic acid tert-butyl ester (638. lmg, 1.906mmol, leq) and 1-methyl-lH- indazol-5-ylamine (567.4mg, 3.855mmol, 2eq) in W-BuOH (26mL) was stirred at 12O⁰C for 15h. A white precipitate was filtered off, washed several times with MeOH, and dried under high vacuum, giving the title compound, as a white solid. The filtrate was adsorbed onto Hydromatrix, dry loaded, and purified by chromatography on silica gel [Jones Flashmaster, 2Og / 7OmL cartridge, eluting with MeOH:DCM 2% → 4% ->• 6%]. Fractions containing product were combined and concentrated in vacuo, affording a second batch of the title compound, as a brown solid. ¹H ΝMR (400 MHz, DMSO-J₆): δ = 1.44 (s, 9H), 2.43-2.53 (m, 2H), 3.57 (t, J= 5.6 Hz, 2H), 4.03 (s, 5H), 6.38 (s, br, IH), 6.76 (s, br, IH), 8.60 (d, J= 8.8 Hz, IH), 7.69 (dd, J= 8.8, 2.0 Hz, IH), 8.01 (d, J= 0.8 Hz, IH), 8.26 (s, IH), 8.39 (d, J= 1.6 Hz, IH)₅ 9.34 (s, -NH), 11.91 (d, J= 2.0 Hz, -NH). MS (ES+): m/z 446.07 (100) [MH⁺]. HPLC: *_R = 2.59 min (ZQ2000, polar_5min).

[866] EXAMPLE 290: (l-Methyl-lH-indazoI-S-ylHό-CMΛδ-tetrahydro- pyridin-4-yI)-7H-pyr rolo [2,3-rf] pyrimidin-4-yl] -amine ήis-hydrochloride.

[867] A 4.0M solution of HCl in 1,4-dioxane (4.7mL; 20eq) was added to a suspension of 4-[4-(l-methyl-lH-indazol-5-ylamino)-7H-pyrrolo[2,3-J]pyrimidin-6-yl]-3,6- dihydro-2H-pyridine-l-carboxylic acid tert-buty\ ester (415.4mg, 0.9324mmol, leq) in 1,4- dioxane (8mL) and stirred at rt for 2h. The solid was filtered off, washed several times with dioxane, and dried under vacuum, yielding the title compound, as a yellow solid. ¹H NMR (400 MHz, DMSO-^₆): δ = 2.65 (s, br, 2H), 3.32 (s, br, 2H), 3.80 (s, br, 2H), 4.11 (s, 3H), 6.50 (s, IH), 7.04 (s, br, IH), 7.51 (dd, J= 8.8, 1.6 Hz, IH), 7.83 (d, J= 9.2 Hz, IH), 7.98 (s, IH), 8.15 (s, IH), 8.26 (s, IH), 9.43 (s, br, -NH + -NH), 11.56 (s, br, -NH), 13.09 (s, H⁺). MS (ES+): m/z 346.16 (31) [MH⁺]. HPLC: /_R = 1.57 min (ZQ2000, polar_5min). [868] EXAMPLE 291: 4-[4-(l-MethyI-lJΪ-indazol-5-yIamino)-7iy-pyrrolo[2,3- rfJpyrimidin-ό-ylJ-Sjδ-dihydro^H-pyridine-l-carboxylic acid tert-butylamide.

[869] To a suspension of (l-methyl-l/f-indazol-5-yl)-[6-(l,2,3,6-tetrahydropyridin-

4-yl)-7H-ρyrrolo[2,3-J]pyrimidin-4-yl]-amme

(166.8mg, 0.363 lmmol, leq) in anhydrous DMF (17mL), N,N-diisopropylethylamine (DiPEA) (260μL, 4.1eq) was added at rt. The solution was then cooled to -20⁰C, after which tert-hutyl isocyanate (36.5mg, 0.368mmol, leq in anhydrous DMF (2mL) was added. The solution was stirred at rt for Ih. The reaction was cooled to 0⁰C, after which additional tert-butyl isocyanate (11.4mg, 0.115mmol, 0.3eq) in anhydrous DMF (ImL) was added. The reaction was stirred again at rt for 4h. The reaction was quenched with MeOH, concentrated in vacuo, and dried under vacuum pressure. The crude material was adsorbed onto Hydromatrix, dry loaded, and purified by chromatography on silica gel [Jones Flashmaster, 5g / 25mL cartridge, eluting with MeOH:DCM 1 % -» 5%]. Fractions containing product were combined and concentrated in vacuo. The material was further purified by trituration in MeOH, yielding the title compound as an off-white solid. ¹H ΝMR (400 MHz, DMSO-^₆): δ = 1.28 (s, 9H), 2.44 (S₃ br, 2H), 3.52 (t, J= 5.6 Hz, 2H), 3.99 (d, /= 2.0 Hz, 2H), 4.03 (s, 3H), 5.77 (s, -NH), 6.40

(s, br, IH), 6.75 (s, IH), 7.60 (d, J= 8.8 Hz, IH), 7.69 (dd, J= 8.8, 2.0 Hz, IH), 8.01 (s, IH),

8.26 (s, IH), 8.39 (s, IH), 9.32 (s, -NH), 11.89 (s, -NH). MS (ES+): m/z 445.07 (100)

[MH⁺]. HPLC: f_R = 2.29 min (ZQ2000, polar_5min).

[870] EXAMPLE 292: l-{4-[4-(l-Methyl-lH-indazoI-5-ylamino)-7iϊ- pyrrolo[2,3-d]pyrimidiii-6-yl]-3,6-dihydro-2/r-pyridin-l-yl}-3-piperidin-l-yI-proρan-l- one.

[871] To a suspension of (l-methyl-lH-indazol-5-yl)-[6-(l,2,3,6-tetrahydro- pyridin-4-yl)-7H-pyrrolo[2,3-rf]pyrimidin-4-yl]-amine ^-hydrochloride (155.3mg, 0.3381mmol, leq), 1-piperidinepropanoic acid (150. lmg, 0.9548mmol, 2.8eq), 1- hydroxybenzotriazole (ΗOBt) (46.7mg, 0.346mmol, leq), and PS-carbodiimide (1.37mmol/g loading; 1008.7mg, 1.38mmol, 4eq) in anhydrous DMF (1OmL), DiPEA (290μL, 1.7mmol, 5eq) was added and was shaken at rt for 13h. The resin was filtered off and rinsed several times with DMF. The filtrate was concentrated in vacuo at medium temp (bath temp: max 42° C), redissolved in MeOH and DCM, and concentrated again under reduced pressure. The crude material was adsorbed onto Ηydromatrix, dry loaded, and purified by chromatography on silica gel [Jones Flashmaster, 1Og / 7OmL cartridge, eluting with MeOΗ:DCM 5% -» 10% -» 7N NH₃(MeOH):DCM 3% -> 5%]. Fractions containing product were combined and concentrated in vacuo, affording the title compound as an off-white solid. ¹H NMR (400 MHz, DMSCW₆): S = 1.30-1.40 (m,, 2H), 1.45-1.53 (m,, 4H), 2.30-2.41 (s, br, 4H), 2.41- 2.63 (m, 6H), 3.69 (t, J= 5.6 Hz, 2H), 4.03 (s, 3H), 4.23 & 4.13 (s, br, rotamers, 2H), 6.41 (s, br, IH), 6.75 & 6.77 (s, br, rotamers, IH), 7.60 (d, J= 9.2 Hz, IH), 7.69 (dd, J= 8.8, 2.0 Hz, IH), 8.01 (s, IH), 8.26 (d, J= 2.0 Hz, IH), 8.38 & 8.39 (s, br, rotamers, IH), 9.34 (s, -NH), 11.90 & 11.93 (s, rotamers, IH). MS (ES+): m/z 485.11 (45) [MH⁺]. HPLC: f_R = 1.72 mm (ZQ2000, polar_5min).

[872] EXAMPLE 293: 2-(2-Methoxyethoxy)-l-{4-[4-(l-methyl-lH-indazol-5- ylamino)-7Jϊ-pyrrolo[2,3-rf]pyriniidin-6-yl]-3,6-dihydro-2H-pyridin-l-yl}-ethanone.

[873] The title compound was obtained following the procedure for l-{4-[4-(l- methyl-lH-indazol-5-ylarruno)-7H-pyrrolo[2,3-^ρyrirnidin-6-yl]-3,6-dihydro-2H-pyridin-l- yl}-3-piperidin-l-ylρropan-l-one, using (2-methoxyethoxy)-acetic acid, and triturating the crude material once in MeOH, as an off-white solid. ¹H NMR (400 MHz, DMSO-^₆): δ = 2.44-2.61 (s, br, rotamers, 2H), 3.25 (s, 3H), 3.45-3.50 (m, 2H), 3.55-3.60 (m, 2H), 3.64 & 3.70 (t, /= 5.2 Hz, rotamers, 2H), 4.03 (s, 3H), 4.13 & 4.16' (s, br, rotamers, 2H)₅4.20 & 4.24 (s, rotamers, 2H), 6.40 (s, br, IH), 6.75 & 6.78 (s, br, rotamers, IH), 7.60 (d, J= 8.8 Hz, IH), 7.67 (dd, /= 8.8, 2.0 Hz, IH), 8.01 (s, IH), 8.26 (s, IH), 8.38 & 8.39 (s, br, rotamers, IH), 9.34 (s, -NH), 11.91 & 11.94 (s, rotamers, -NH). MS (ES+): m/z 462.08 (100) [MH⁺]. HPLC: ^_R = 1.99 min (ZQ2000, polar_5min).

[874] EXAMPLE 294: {4-[4-(l-Methyl-lH-indazol-5-ylamino)-7_Jfir- pyrrolo[2,3-rf|pyrimidin-6-yI]-3,6-dihydro-2iϊ-pyridin-l-yl}-(4-methylpiperazin-l-yl)- methanone.

[875] To a suspension of (l-methyl-lH-indazol-5-yl)-[6-(l ,2,3,6-tetrahydropyridin-

4-yl)-7H-pyrrolo[2,3-rf]pyrimidin-4-yl]-amine /rø-hydrochloride (78.1mg, 0.172mmol, leq) in DMF (5mL), DiPEA (180μL, l.Ommol, 6eq) was added. After cooling the suspension to 0⁰C, 4-methyl-l-piperazinecarbonyl chloride hydrochloride (28.6mg, 0.170mmol, leq) in DMF (1.5mL) was added and the reaction was stirred at 0°C for 2h. An additional 0.2eq of 4- methyl-1-piperazinecarbonyl chloride hydrochloride (6.1mg, 0.036mmol) in DMF (ImL) was added and the suspension was stirred again at O⁰C for 3h. Still additional acid chloride was needed and 4-methyl-l-piperazinecarbonyl chloride hydrochloride (6.1mg, 0.036mmol, 0.2eq) in DMF (ImL) was added. After 5 h, the reaction was quenched / worked up as follows: reaction solution was added dropwise into water, filtered (M frit), washed with water and then EtOAc, and dried, giving the title compound as an off-white solid. ¹H NMR (400 MHz, DMSO-^₆): S = 2.19 (s, 3H), 2.31 (s, br, 4H), 2.44-2.55 (m, 2H), 3.17 (s, br, 4H), 3.40 (t, J= 5.2 Hz, 2H), 3.92 (s, br, 2H), 4.03 (s, 3H), 6.38 (s, br, IH), 6.75 (s, IH), 7.60 (d, J= 8.4 Hz, IH), 7.69 (d, J= 8.8 Hz, IH), 8.01 (s, IH), 8.25 (s, IH), 8.38 (s, br, IH), 9.33 (s, -NH), 11.89 (s, -NH). MS (ES+): m/z 472.14 (9) [MH⁺]. HPLC: t_R = 1.68 min (ZQ2000, polar_5mm).

[876] EXAMPLE 295: 4-4-[2-(2-Dimethylaminoethylamino)-benzothiazol-6- ylamino]-7H-pyrrolo[2,3-rf]pyriniidin-6-yl-3,6-dihydro-2H-pyridine-l-carboxylic acid fert-butyl ester.

[877] To a suspension of N^I2¹-(2-dimethylaminoethyl)-N^l6^I-[6-(l ,2,3,6- tetrahydropyridin^-yl)-7H-pyrrolo[2,3-J]pyrimidin-4-yl]-benzothiazole-2,6-diamine (221. lmg, 0.346mmol, leq) in anhydrous DCM (5mL) and anhydrous DMF (4mL), DiPEA (425/dL., 2.43mmol, 7eq) was added under an atmosphere of N₂. A solution of άi-tert- butyldicarbonate (78.2mg, 0.355mmol, leq) in anhydrous DCM (3mL) and anhydrous DMF (0.5mL) was added via syringe. The reaction was allowed to stir at rt for 2h, after which it was concentrated in vacuo. The crude material (352.4mg) was adsorbed onto Hydromatrix, dry loaded, and purified by chromatography on silica gel [Jones Flashmaster, 1Og / 7OmL cartridge, eluting with neat EtOAc → MeOHiEtOAc 5% → 7N NH₃/MeOH:EtOAc 2% -» 5%]. Fractions containing product were combined, concentrated in vacuo, and further purified by HPLC, affording the title compound as a yellow solid. ¹H NMR (400 MHz, MeOH-^): δ = 1.50 (s, 9H), 2.33 (s, 6H), 2.54 (s, br, 2H), 2.66 (t, J= 6.4 Hz, 2H), 3.59 (t, J = 6.4 Hz, 2H), 3.65 (s, br, 2H), 4.12 (s, br, 2H), 6.27 (s, br, IH), 6.55 (s, IH), 7.42 (d, J= 1.2 Hz, 2H), 8.05 (d, J = 0.8 Hz, IH), 8.17 (s, IH). MS (ES+): m/z 534.92 (95) [MH⁺]. HPLC: *_R = 2.07 min (ZQ2000, polar_5min).

[878] iV2'-(2-DimethyIaminoethyl)-iV6'-[6-(l,2,3,6-tetrahydropyridin-4-yl)-

7iϊ-pyrrolo [2β-d] pyrimidin-4-yl] -benzothiazole-2,6-diamine.

[879] A solution of N2'-(2-dimetiiylaminoethyl)-benzothiazole-2,6-diamine

(64.4mg, 0.267mmol, leq), 4-(4-chloro-7H-pyrrolo[2,3-d]pyrimidin-6-yl)-3,6-dihydro-2H- pyridine-1-carboxylic acid tert-butyl ester (95.8mg, 0.286mmol, leq), and trifluoroacetic acid (TFA) (104//L, 1.34mmol, 5eq) in 2,2,2-trifluoroetlianol (TFE) (4mL), in a sealed tube, was stirred at 100⁰C for 3.5h and concentrated in vacuo, giving the crude title compound. No workup or purification was performed prior to N-BOC protection. MS (ES+): m/z 434.92 (15) [MH⁺]. HPLC: /_R = 0.49 & 1.40 min (ZQ2000, polar_5min). [880] 7V2'-(2-Dimethylaminoethyl)-benzothiazole-2,6-diamine

[881] To a suspension of NN-dimethyl-N'-(6-nitrobenzothiazol-2-yl)-ethane-l,2- diamine (190.3mg, 0.707mmol, leq) in MeOH (9mL) and Pd/C (10%, 50% H₂0, 0.06eq), H₂ _(g) was introduced into the system and the reaction was allowed to stir for 4h at rt. Pd/C was filtered over a pad of Celite and rinsed with MeOH. The filtrate was concentrated in vacuo, yielding the title compound as a hard, yellow, plastic-like solid. ¹H ΝMR (400 MHz, MeOH- d₄): δ = 2.34 (s, 6H), 2.65 (t, J= 6.4 Hz, 2H), 3.53 (t, J= 6.4 Hz, 2H), 6.72 (dd, J= 8.4, 2.4 Hz, IH), 6.98 (d, J= 2.4 Hz, IH), 7.21 (d, J= 8.4 Hz, IH). MS (ES+): m/z 237.20 (89) [MH⁺]. HPLC: t_κ = 0.33 min (ZQ2000, polar_5min). [882] iV,7V-Dimethyl-iV-(6-nitrobenzothiazol-2-yl)-ethane-l,2-dianiine

[883] To a solution of 2-bromo-6-nitrobenzothiazole (195.2mg, 0.7384mmol, leq) in THF (8mL) N,N-dimethyl-l,2-ethanediamine (405 μL, 3.69mmol, 5eq) was added. The reaction was stirred for Ih at rt, after which all solvent was evaporated in vacuo. The residue was dissolved in DCM and washed with NaHCO₃ (2x) and brine (1 x). The filtrate was dried over Na₂SO₄, filtered, and concentrated under reduced pressure. The yellow crude material was adsorbed onto Hydromatrix and purified by chromatography on silica gel [Jones Flashmaster, 5g / 25mL cartridge, eluting with 1:1 EtOAc:DCM -» 3% MeOH:DCM]. Fractions 19-61 were combined and concentrated in vacuo, affording the title compound as a yellow solid. ¹H NMR (400 MHz, CDCl₃): δ = 2.29 (s, 6H), 2.60 (t, J= 6.0 Hz, 2H), 3.54 (q, br, J= 4.8 Hz, 2H), 6.39 (s, br, -NH), 7.52 (d, J= 8.8 Hz, IH), 8.20 (dd, J= 8.8, 2.0 Hz, IH), 8.50 (d, J= 2.0 Hz, IH). MS (ES+): m/z 267.10 (100) [MH⁺]. HPLC: t_κ = 1.78 min (ZQ2000, polar_5min). [884] 2-Brorao-6-nitrobenzothiazole

[885] Into a 15OmL beaker, 2-amino-6-nitrobenzothiazole (5.1089g, 25.39mmol, leq) was mixed vigorously with phosphoric acid, 85 wt. % (22.6mL, 13eq) at 50 ⁰C. The solution was then cooled to -20°C, using an acetone / dry ice bath. To this, a solution of NaNO₂ (1.943g, 28.16mmol, l.leq) in water (5.OmL), also cooled to -20⁰C, was added slowly over the course of 15min. After 1 h, the resulting suspension was poured over a solution of CuBr (4.593g, 32.02mmol, 1.3eq) in 48% HBr (25.3mL) at rt and was stirred. Additional HBr (« 35mL) aided in transfer. After Ih, the mixture was heated at 4O⁰C for 2h. After 2h, the heat was turned off and the reaction continued to stir at rt for 16h. The crude mixture was diluted with water to a final volume of 20OmL and was extracted with DCM (3x). The organics were dried over anhydrousmg₂SO₄, filtered, and concentrated under reduced pressure. The crude material was adsorbed onto silica gel, dry loaded, and purified by chromatography on silica gel [Jones Flashmaster, 5Og / 15OmL cartridge, eluting with DCM/Hex 1:1 — > 2:1 — > neat DCM] . Fractions containing product were combined, concentrated in vacuo, and re-chromatographed to give the title compound as an orange solid. ¹H NMR (400 MHz, CDCl₃): δ = 8.11 (d, J= 9.2 Hz, IH), 8.38 (dd, J- 9.2, 2.4 Hz, IH), 8.78 (d, J = 2.0 Hz, IH). MS (ES+): m/z 258.95/260.96 (100/96) [MH⁺]. HPLC: *_R = 3.43 min (ZQ2000, polar_5min).

[886] EXAMPLE 296: 4-[4-(2-BenzylaminobenzothiazoI-6-yIamino)-7iϊ- pyrrolo[2,3-rfjpyrimidin-6-yI]-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-bnty\ ester.

[887] The title compound was prepared following the procedure for 4-4-[2-(2- dimethylaminoethylamino)-benzothiazol-6-ylamino]-7H-pyrrolo[2,3-d]pyrimidin-6-yl-3,6- dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester, using N'2'-benzyl-N'6'-[6-(l,2,3,6- tetrahydropyridm^-yl)-7H-pyπ-olo[2,3-^pyrirnidin-4-yl]-benzothiazole-2,6-diamine, except that additional equivalents (2eq total) of BOC-anhydride were used, no DiPEA was used, and the material was purified only by column chromatography. Yellow gum. ¹H ΝMR (400 MHz, CDCl₃): δ = 1.49 (s, 9H),2.42 (br, s, 2H), 3.62 (br, t, J= 5.2 Hz, 2H), 4.14 (br, s, 2H), 4.66 (s, 2H), 5.91 (br, s, IH), 6.04 (br, s, -NH), 6.18 (br, s, IH), 7.30-7.44 (m, 6H + -NH), 7.54 (d, J= 8.4 Hz, IH), 7.95 (br, s, IH), 8.30 (br, s, IH), 11.51 (br, s, -NH). MS (ES+): m/z 553.94 (100) [MH⁺]. HPLC: fo = 3.03 min (ZQ2000, polar_5min). [888] iV2'-Benzyl-iV6'-[6-(l,2,3,6-tetrahydropyridin-4-yl)-7H-pyrrolo[2,3- d\ py rimidin-4-yl] -benzothiazole-2,6-diamine.

[889] The title compound was prepared following the procedure for N"2'-(2- dimethylaminoethyl)-N6'-[6-(l,2,3,6-tetrahydropyridin-4-yl)-7H-pyrrolo[2,3-J]pyrirnidin-4- yl]-benzothiazole-2,6-diamine, using N2'-benzylbenzothiazole-2,6-diamine, except for the following modifications: The reaction was heated for 18h at 100⁰C. The residue was dissolved in a 5% MeOΗ:DCM mixture and washed with NaHCO₃ (Ix) and brine (Ix), dried over anhydrous Na₂SO₄, filtered, and concentrated in vacuo. Any emulsion was dissolved in additional 5% MeOH:DCM and washed in the same manner. The crude material was adsorbed onto Hydromatrix, dry loaded, and purified by chromatography on silica gel [Jones Flashmaster, 2g / 2OmL cartridge, eluting with MeOH:DCM 5% (1-24) → 10% (25-41) → 7N NH₃/Me0H:DCM 5% (42-57) → 10% (58+)]. Fractions containing product were combined and concentrated under reduced pressure, affording the title compound. ¹H NMR (400 MHz, DMSO-J₅): δ = 2.48 (d, J= 2.4 Hz, 2H), 3.06 (t, J= 6.0 Hz, 2H), 3.51 (d, J= 2.8 Hz, 2H), 4.54 (s, 2H), 6.23 (s, br, IH), 6.45 (s, br, IH), 7.13-7.20 (m,, IH), 7.22-7.28 (In₀, 2H), 7.28-7.33 (m, 4H), 7.92-7.97 (m, IH), 8.07 (s, IH). MS (ES+): m/z 453.98 (13) [MH⁺- BOC]. HPLC: t_R = 2.11 min (MDP [Waters / Micromass], polar_5min). [890] iV2'-BenzyIbenzothiazoIe-2,6-diamine

[891] The title compound was prepared following the procedure for N2'-(2- dimethylaminoethyl)-benzothiazole-2,6-diamine, using benzyl-(6-nitrobenzothiazol-2-yl)- amine. Brown solid. ¹H ΝMR (400 MHz, CDCl₃): 5 = 3.56 (s, br, -NH₂), 4.61 (s, 2H), 5.25 (s, br, -NH), 6.69 (dd, /= 8.4, 2.4 Hz, IH), 6.93 (d, J= 2.4 Hz, IH), 7.28-7.42 (m, 6H). MS (ES+): m/z 256.19 (100) [MH⁺]. HPLC: t_κ = 2.01 min (ZQ2000, polarjmin). [892] BenzyI-(6-nitrobenzothiazol-2-yl)-amine

[893] The title compound was prepared following the procedure for JV,./V-dimethyl-

N-(6-nitrobenzothiazol-2-yl)-ethane-l ,2-diamine, using benzylamine. Modified workup: Solid that had precipitated during course of reaction (amine salt) was filtered; no aqueous workup was conducted. ¹H NMR (400 MHz, CDCl₃): δ = 4.70 (s, 2H), 6.07 (s, br, -NH), 7.33-7.39 (m, IH), 7.39-7.42 (m, 4H), 7.51 (d, J= 8.8 Hz, IH), 8.21 (dd, J= 8.8, 2.4 Hz, IH), 8.5 l (d, J = 2.4 Hz, IH). MS (ES+): m/z 286.03 (100) [MH⁺]. HPLC: t_κ = 3.47 min (ZQ2000, polar_5min).

[894] EXAMPLE 297: 4-[4-(2-Phenethylamiπobenzothiazol-6-ylamino)-7.ff- pyrroIo[2,3-rf]pyrimidin-6-yl]-3,6-dihydro-2J3-pyridine-l-carboxyIic acid tert-bntyl ester.

[895] The title compound was prepared following the procedure for 4-4-[2-(2- dimethylammoeώylarrmo)-benzoώiazol-6-ylamώo^ dihydro^H-pyridine-l-carboxylic acid tert-bnty\ ester, using 7V2'-phenethyl-N^l6'-[6-(l,2,3,6- tetoahydropyridin4-yl)-7H-pyπ:olo[2,3-d]pyrirrddin-4-yl]-benzo1hiazole-2,6-diamine. Off- white solid. ¹H ΝMR (400 MHz, DMSO-(Z₁₅): δ = 1.43 (s, 9H), 2.43-2.48 (s, br, 2H), 2.92 (t, J= 6.8 Hz, 2H), 3.53-3.63 (m, 4H), 4.03 (s, br, 2H), 6.38 (s, br, IH), 6.73 (s, IH), 7.19-7.24 (m, IH), 7.26-7.34 (m, 4H), 7.36 (d, J= 8.4 Hz, IH), 7.52 (dd, J= 8.8, 2.4 Hz, IH), 7.99 (t, J = 5.2 Hz, -NH), 8.24 (s, IH), 8.31 (d, J= 2.4 Hz, IH), 9.30 (s, -NH), 11.90 (s, -NH). MS (ES+): m/z 567.98 (77) [MH⁺]. HPLC: *_R = 3.02 irnn (ZQ2000, polar_5min). [896] iV2'-Phenethyl-iV6'-[6-(l,2,3,6-tetrahydropyri(iin-4-yl)-7H-pyrrolo[2,3-

<flpyrimidin-4-yl]-benzothiazoIe-2,6-diamine.

[897] The title compound was prepared following the procedure for N2'-(2- dimethylaminoethyl)-N'6'-[6-(l ,2,3 ,6-tetrahydropyridin-4-yl)-7H-pyrrolo[2,3 -<f]pyrimidin-4- yl]-benzomiazole-2,6-diamine, using N2'-phenethylbenzothiazole-2,6-diamrne. MS (ES+): m/z 467.96 (25) [MH⁺]. HPLC: fe = 2.01 min (ZQ2000, polar_5min). [898] iV2'-PhenethylbenzothiazoIe-2,6-diamine

[899] The title compound was prepared following the procedure for N¹2'-(2- dimethylaminoethyl)-benzotliiazole-2,6-diamine, using (6-nirrobenzothiazol-2-yl)- phenethylamine. Brown gum. ¹H ΝMR (400 MHz, CDCl₃): δ = 2.98 (t, J= 6.8 Hz, 2H), 3.58 (s, br, -NH₂), 3.67 (q, J= 6.8 Hz, 2H), 4.92 (s, br, -NH), 6.68 (dd, J= 8.4, 2.4 Hz, IH), 6.94 (d, J= 2.4 Hz, IH), 7.21-7.37 (m, 6H). MS (ES+): m/z 270.13 (100) [MH⁺]. HPLC: h = 2.10 min (ZQ2000, polar_5min). [900] (6-Nitrobenzothiazol-2-yl)-phenethylamine

[901] The title compound was prepared following the procedure for iV,JV-dimethyl-

N'-(6-nitrobenzothiazol-2-yl)-ethane-l,2-diamine, using 4 eq of phenethylamine. Modified workup: Solid that had precipitated during course of reaction (amine salt) was filtered; no aqueous workup was conducted. ¹H ΝMR (400 MHz, CDCl₃): δ = 3.03 (t, J= 6.4 Hz, 3H), 3.77 (q, J= 6.4 Hz, 2H), 7.23-7.30 (m, 3H), 7.33-7.38 (m, 2H), 7.52 (d, J= 8.8 Hz, IH), 8.21 (dd, J= 8.8, 2.4 Hz, IH), 8.51 (d, J= 2.4 Hz, IH). MS (ES+): m/z 300.10 [MH⁺]. HPLC: t_R = 3.57 min (ZQ2000, polar_5min).

[902] EXAMPLE 298: 4-4-[2-(2-Methoxyethylamino)-benzothiazoI-6- ylaminol-TH-pyrroIotljS-rflpyrimidin-β-yl-S^-dihydro-lH-pyridine-l-carboxy lie acid tert-butyi ester.

[903] The title compound was prepared following the procedure for 4-4-[2-(2- dimemylammoemylarmno)-benzomiazol-6-ylamino]-7H-pyrrolo[2,3-d]pyrirrύdin-6-yl-3,6- dihydro-2H~pyridine-l-carboxylic acid tert-hutyl ester, using N2'-(2-methoxyethyl)-N'6'-[6-

(l,2,3,6-telxahydropyridin4-yl)-7H-pyrrolo[2,3-<ήpyrimidin-4-yl]-benzothiazole-2,6-diamme.

Tan solid. ¹HNMR (400 MHz, DMSO-J₀): δ = 1.43 (s, 9H), 2.43-2.48 (m, 2H), 3.29 (s,

3H), 3.52 (d, J= 2.8 Hz, 4H), 3.56 (t, J= 5.6 Hz, 2H), 4.00-4.07 (m, 2H), 6.38 (br, s, IH),

6.73 (s, IH), 7.34 (d, J= 8.4 Hz, IH), 7.52 (dd, J= 8.8, 2.4, IH), 8.00 (br, s, -NH), 8.23 (s,

IH), 8.29 (d, J= 2.0 Hz, IH), 9.30 (s, -NH), 11.91 (s, -NH). MS (ES+): m/z 521.90 (96)

[MH⁺]. HPLC: t_R = 2.54 min (ZQ2000, polar_5min).

[904] iV2'-(2-Methoxyethyl)-iV¹6^I-[6-(l,2,3,6-tetrahydropyridm-4-yl)-7H- pyrrolo[2,3-rf]pyriraidin-4-yl]-benzothiazoIe-2,6-diamine.

[905] The title compound was prepared following the procedure for iV2'-(2- dimethyIaminoethyl)-N6'-[6-(l,2,3,6-tetrahydropyridin-4-yl)-7H-pyrroIo[2,3-cTlpyrimidin-4- yl]-benzothiazole-2,6-diamine, using N'2'-(2-methoxyethyl)-benzothiazole-2,6-diamine, except that the reaction mixture was heated for 45h to 100 ⁰C. MS (ES+): m/z 421.94 (61) [MH⁺]. HPLC: t_κ = 0.50 & 1.62 min (ZQ2000, polar_5min). [906] iV2'-(2-Methoxyethyl)-benzothiazoIe-2,6-diamine

[907] The title compound was prepared following the procedure for 7V2'-(2- dimethylaminoethyl)-benzothiazole-2,6-diamine, using (2-methoxyethyl)-(6-nitro- benzothiazol-2-yl)-amine. Pink solid. ¹H NMR ^OO MHZ₅ CDCI₃): δ = 3.39 (S, 3H), 3.58 (S, br, -NH₂), 3.62 (s, 4H), 5.26 (s, br, -NH), 6.68 (dd, J= 8.4, 2.4 Hz, IH), 6.92 (d, J= 2.0 Hz, IH), 7.35 (d, J= 8.8 Hz, IH). MS (ES+): m/z 224.21 (100) [MH⁺]. HPLC: *_R = 0.49 & 1.05 min (ZQ2000, polar_5min).

[908] (2-Methoxyethyl)-(6-nitrobenzothiazol-2-yl)-amine

[909] The title compound was prepared following the procedure for N,N-dimethyl-

N-(6-nitrobenzothiazol-2-yl)-ethane-l,2-diamine, using 6.78 eq of 2-methoxyethylamine. ¹H ΝMR (400 MHz, CDCl₃): δ = 3.42 (s, 3H), 3.65 (td, J= 4.4, 0.8 Hz, 2H), 3.70 (t, br, J= 4.4 Hz, 2H), 5.92 (s, br, -NH), 7.53 (d, J= 8.8 Hz, IH), 8.21 (dd, J= 9.2, 2.4 Hz, IH), 8.51 (d, J = 2.4 Hz, IH). MS (ES+): m/z 254.10 (100) [MH⁺]. HPLC: fe = 2.89 min (ZQ2000, polar_5min).

[910] EXAMPLE 299: tert-Butyl 4-[4-(4-methoxy-3-thiazoI-5-yIphenyIamino)-

7H~pyrrolo[2,3-^pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l-carboxylate.

[911] Nitrogen was bubbled through a solution of tert-butyl 4-[4-(3-iodo-4- methoxyphenylamino)-7H-pyrrolo[2,3-(^pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l- carboxylate (109.5 mg, 0.2 mmol), thiazole (85.1 mg, 1.0 mmol), potassium acetate (39.3 mg, 0.4 mmol), and tetrakis(triphenylphosphine)-palladium (23.1 mg, 0.02 mmol) in DMF (0.8 mL) for 3 min. The mixture was then heated to 100⁰C and stirred for 17 h. The solvents were removed in vaccuo and the residue was dissolved in DMF (~2 mL). The DMF solution was filtered and sent to mass-directed HPLC purification to give the title compound. ¹H-NMR (CD₃OD, 400 MHz): δ = 1.50 (s, 9 H), 2.55 (m, 2 H), 3.66 (m, 2 H), 3.98 (s, 3 H), 4.13 (m, 2 H), 6.28 (s, br, 1 H), 6.60 (s, 1 H), 7.17 (d, J= 9.2 Hz, 1 H), 7.68 (dd, J= 2.4, 8.8 Hz, 1 H), 8.06 (d, J= 2.8 Hz, 1 H), 8.20 (s, 1 H), 8.31 (s, 1 H), 8.98 (s, 1 H). MS (ES+): m/z 504.99 (MH⁺). HPLC: t_R = 2.95 min (ZQ2000, polar_5min). The following EXAMPLES 300-301 are compounds of Formula (I) wherein X = C-CN. [912] EXAMPLE 300: 4-[5-Cyano-4-(lH-indazol-5-ylamino)-lH-pyrrolo[2,3-

6]pyridin-2-yI]-3,6-dihydro-2H-pyridine-l-carboxyIic acid tert-butyl ester.

[913] To a mixture of 4-[5-bromo-4-(l#-indazol-5-ylamino)-lH-pyrrolo[2,3-

&]pyridin-2-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid ter/-butyl ester (8mg, 0.015mmol), DPPF (4.1mg, 0.007mmol), water (0.03mL) and zinc cyanide (3.7mg, 0.031mmol) in acetonitrile (3mL) was added Pd₂dba₃ (3.6mg, 0.004mmol) and the mixture was heated to reflux under N₂ overnight. The reaction mixture was evaporated and the crude product was purified by preparative TLC using 10% methanol in DCM as eluent to afford 4-[5-cyano-4- (lH4ndazol-5-ylardno)-lH-pyrrolo[2,3-6]pyridin-2-yl]-3,6-dihydro-2H-pyridine-l- carboxylic acid fert-butyl ester as light gray solid. ¹H NMR (400 MHz, CD₃OD): δ = 8.05 (s, IH), 7.96 (s, IH), 7.62 (άά,J= 1.8, 0.5 Hz, IH), 7.50 (s, IH), 7.27 (dd, J= 8.8, 1.9 Hz, IH), 6.05 (bs, IH), 5.35 (bs, IH), 3.93-3.97 (m, 2H), 3.40 (t, J= 6.2 Hz, 2H), 2.02-2.07 (m, 2H), 1.37 (s, 9H); MS (ES+): mlz 455.99 (100) [MH⁺]; HPLC: t_R = 2.97 min (ZQ2000, polar_5min).

[914] 4-[5-Bromo-4-(ljy-indazoI-5-ylamino)-l_JH^r-pyrroIo[2,3-6]pyridin-2-yl]-

3,6-dihydro-2Jϊ-pyridine-l-carboxylic acid tert-bntyl ester

[915] To a mixture of (5-bromo-2-iodo-lH-pyrrolo[2,3~&]pyridin-4~yl)-(lH- indazol-5-yl)-amine (25mg, 0.069mmol), potassium carbonate (19mg, 0.14mmol), tetrakistriphenylphosphine palladium (10mg, 0.014mmol) and 4-(4,4,5,5-tetramethyl- [l,3,2]dioxaborolan-2-yl)-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester (21.6mg, 0.069mmol) was added degassed DMF (3mL) and water (0.75mL) and the mixture was heated to reflux for 5h. Water was added to the reaction and filtered. The precipitate was washed with water and the filtrate was extracted with DCM. The precipitate was dissolved in DCMMeOH mixture (9:1) and combined with the DCM extract and evaporated. The crude product was purified by preparative TLC using 8 % methanol in DCM as eluent to afford the title compound as beige solid. ¹H NMR (400 MHz, CD₃OD): δ = 10.32 (s, IH), 8.11 (s, IH), 8.02 (s, IH), 7.58 (d, /= 0.8 Hz, IH), 7.47 (d, J= 8.9 Hz, IH), 7.26 (dd, /= 8.8, 1.9 Hz, IH), 6.69 (s, IH), 5.95 (bs, IH), 5.16 (bs, IH), 3.99-4.03 (m, 2H), 3.42 (t, J= 5.4 Hz, 2H), 2.00- 2.07 (m, 2H), 1.39 (s, 9H); MS (ES+): m/z 510.89 (100) [MH⁺]; HPLC: t_R = 2.63 min (ZQ2000, polar_5min). [916] (5-Bromo-2-iodo-lH-pyrrolo[2,3-A]pyridin-4-yl)-(li3^:-indazol-5-yl)-amine

[917] To a slurry of a mixture of l-benzenesulfonyl-5-bromo-4-chloro-2-iodo-lH- ρyrrolo[2,3-έ]pyridine and 5-bromo-4-chloro-2-iodo-l-(2-iodobenzenesulfonyl)-lH- pyrrolo[2,3-έ]pyridine (560mg, l.Ommol) in trifluoroetlianol (6mL) was added trifluoroacetic acid (0.04ImL, 0.52mmol) and indazole (266mg, 2.0mmol), and the reaction was heated in a sealed tube at 12O⁰C for 4d. Additional indazole (67mg, 0.5mmol) was added twice to the reaction on the second and third days. The reaction was cooled to RT, diluted with methanol (2OmL), saturated sodium bicarbonate solution was added (ImL) and evaporated to dryness under reduced pressure. The residue obtained was triturated with methanol:DCM (1:1) mixture and filtered. The filtrate was evaporated and the crude obtained was purified by chromatography on silica gel [Jones Flashmaster, 7Og / 15OmL cartridge, eluting with DCM:Methanol 100:0 -» 96:4], yielding the product, which was triturated with 4: 1 methanol:DCM mixture and filtered. The precipitate obtained was dried under vacuum to afford the title compound as an off-white solid. The low polar fractions from the column were combined, evaporated and the residue was stirred with 3N NaOH in methanol (2mL) for 30 min and quenched with saturated ammonium chloride solution (2mL). Water (1OmL) was added and filtered to afford additional title compound. MS (ES+): m/z 453.63 (100) [MH⁺]; HPLC: t_R = 2.58 min (ZQ2000, polar_5min).

[918] l-Benzenesulfonyl-5-bromo-4-chIoro-2-iodo-lH-pyrroIo [2,3-6]pyridine &

5-Bromo-4-chIoro-2-iodo-l-(2-iodobenzenesuIfonyI)-lH-pyrroIo[2,3-6]pyridine

[919] To a solution of l-benzenesulfonyl-5-bromo-4-chloro-lH-pyrrolo[2,3-

%yridine (2.585g, 6.95mmol) in anhydrous THF (33OmL) at -78⁰C was added LDA (11.6mL, 1.5 M solution, 17.39mmol), and the mixture was stirred for 30min. A solution of iodine (4.854g, 19.12mmol) in THF (2OmL) was added and stirring was continued for an additional 2h at -78⁰C. The reaction was quenched with aqueous sodium thiosulfate solution and extracted with DCM (4x80mL). The combined DCM layer was washed with brine, dried over anhydrous sodium sulfate and evaporated under reduced pressure. The crude product was purified by chromatography on silica gel [Jones Flashmaster, 7Og / 15OmL cartridge, eluting with hexane:ethyl acetate 100:0 — > 99:2], yielding a mixture of the title compounds. l-Benzenesulfonyl-5-bromo-4-chloro-2-iodo-lH-pyrrolo[2,3-έ]pyridine: MS (ES+): m/z 498.58 (100) [MH⁺], HPLC: t_R = 7.19 min (ZQ2000, nonpolarJ5min). 5-Bromo-4-chloro-2- iodo-l-(2-iodobenzenesulfonyl)-lH-pyrrolo[2,3-6]pyridine: MS (ES+): m/z 624.41 (100) [MH⁺], HPLC: /_R = 7.58 min (ZQ2000, nonpolar_15min). [920] l-Benzenesulfonyl-5-bromo-4-cliloro-li?-pyrroIo[2,3-ά]pyridine

[921] To a solution of 5-bromo-4-chloropyrrolopyridine (248mg, 1.07mmol) in

THF (5mL) at O⁰C was added sodium hydride (39mg, l.δmmol) and the mixture was stirred for 15min. Benzenesulfonyl chloride (227mg, 1.28mmol) was added and the mixture was allowed to warm to RT and stirred for 4h. Water was added to the reaction mixture and extracted with DCM (3x25mL). The combined DCM layer was washed with brine, dried over anhydrous sodium sulfate and evaporated under reduced pressure. The crude product obtained was purified by chromatography on silica gel [Jones Flashmaster, 5Og / 15OmL cartridge, eluting with hexane:ethylacetate 100:0 -> 95:05], yielding the title compound as colorless solid. ¹H NMR (400 MHz, CDCl₃): δ = 8.50 (s, IH), 8.16-8.19 (m, 2H), 7.77 (d, J = 4.0 Hz, IH), 7.59-7.64 (m, IH), 7.49-7.53 (m, 2H), 6.69 (d, J= 4.0 Hz, IH); MS (ES+): m/z 372.85 (100) [MH⁺]; HPLC: <_R = 4.39 min (ZQ2000, nonpolar_7min). [922] 5-Bromo-4-chIoro-lJT-pyrrolo[2,3-&]pyridme

[923] To a solution of 5-bromo-4-chloro-l-triisopropylsilanyl-lH-pyrrolo[2,3- δ]pyridine (10. Ig, «14.0mmol; crude material prepared according to Tetrahedron Lett, 2004, 45, 2317-2319) in IPA (25OmL) at O⁰C was added 2N H₂SO₄ (25mL) and the mixture was allowed to warm to RT and stirred overnight. IPA was evaporated at 35 ⁰C and water was added to the residue and neutralized with 2N NaOH. The precipitate foπned was filtered, washed with water followed by hexane, and dried under vacuum to yield the title compound as off-white solid. MS (ES+): m/z 233.01 (100) [MH⁺]; HPLC: t_R = 4.51 min (ZQ2000, polar_15min). [924] EXAMPLE 301: 4-[4-(Benzothiazol-6-ylamino)-5-cyano-lH-pyrrolo[2,3- b] pyridin-2-yI] -3 jό-dihydro^ϋT-pyridine-l-carboxylicacid tert-butyl ester.

[925] To a mixture of 4-[4-(benzothiazol-6-ylamino)-5-bromo-lH-pyrrolo[2,3- δ]pyridin-2-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester (20mg, 0.038mmol), DPPF (lO.lmg, 0.018mmol), water (0.04mL) and zinc cyanide (8.9mg, 0.075mmol) in acetonitrile (4mL) was added Pd₂dba₃ (7.0mg, 0.007mmol) and the mixture was heated to reflux under N₂ overnight. The reaction mixture was evaporated, and the crude product was purified by preparative TLC using 7% methanol in DCM as eluent to afford the title compound as light gray solid. ¹H NMR (400 MHz, CDCl₃): δ = 8.98 (s, IH), 8.22 (s, IH), 8.10 (d, J= 8.6 Hz, IH), 7.78 (d, J= 2.0 Hz, IH), 7.36 (dd, J= 8.6, 2.1 Hz, IH), 6.95 (s, IH), 5.93 (bs, IH), 5.36 (s, IH), 3.99-4.02 (m, 2H), 3.44 (t, J= 5.7 Hz, 2H), 3.42 (d, J= 4.9 Hz, 2H), 2.07-2.12 (m, 2H), 1.39 (s, 9H); MS (ES+): m/z 472.96 (100) [MH⁺]; HPLC: t_κ = 3.25 min (ZQ2000, polar_5min).

[926] 4-[4-(Benzothiazol-6-ylamino)-5-bromo-lH-pyrrolo[2,3-Z»]pyridin-2-yl]-

3,6-dihydro-2H-pyridine-l-carboxylicacid tert-butyl ester

[927] To a mixture (55:45) of benzothiazol-6-yl-[5-bromo-2-(l,2,3,6- teteahydropyridin-4-yl)-lH-pyrrolo[2,3-Z)]pyridin-4-yl]-amine and 5-bromo-4-chloro-2- (l,2,3,6-tetrahydropyridin-4-yl)-lH-pyrrolo[2,3-δ]pyridine (lOlmg, 0.272mmol) in THF (5mL) was added triethylamine (83mg, 0.816mmol), DMAP (5mg) and (Boc)₂O (47mg, 0.215mmol) and the reaction was stirred overnight at RT under N₂. The solvent was evaporated and the residue was purified by preparative TLC using 4% methanol in DCM as eluent to afford a mixture of 4-(5-bromo-4-chloro-lH-pyrrolo[2,3-&]pyridin-2-yl)-3,6- dihydro-2H-ρyridine-l~carboxylic acid tert-butyl ester and the title compound. 4-[4- (Benzothiazol-6-ylarnino)-5-bromo-lH-pyrrolo[2,3-Z7]pyridm-2-yl]-3,6-dihydro-2H-pyridine- 1-carboxylicacid /er/-butyl ester: ¹H NMR (400 MHz, CDCl₃): δ = 8.98 (s, IH), 8.19 (s, IH), 8.11 (d, J= 8.6 Hz, IH), 7.75 (d, J= 2.0 Hz, IH), 7.37 (dd, J= 8.7, 2.1 Hz, IH), 6.81 (s, IH), 6.15 (bs, IH), 5.51 (s, IH), 4.90-4.15 (m, 2H), 3.54 (t, J= 5.3 Hz, 2H), 2.95 (s, IH), 2.88 (s, IH), 2.17-2.25 (m, 2H), 1.47 (s, 9H); MS (ES+): m/z 527.84 (100) [MH⁺]; HPLC: t_κ = 3.30 min (ZQ2000, polar_5min). [928] Benzothiazol-6-yl-[5-bromo-2-(l,2,3,6-tetrahydropyridin-4-yl)-lH- pyrrolo[2,3-ft]pyridin-4-yl]-amine

[929] To a slurry of 4-(5-bromo-4-criloro-lH-pyrrolo[2₎3-δ]pyridin-2-yl)-3₎6- dihydro-2#-pyridine-l-carboxylic acid tert-butyl ester (120mg, 0.29mmol) in trifluoroethanol (9mL) were added trifluoroacetic acid (0.112mL, 1.46mmol) and 6-benzothiazolamine ( 58mg, 1.5mmol), and the reaction was heated in a sealed tube at 12O⁰C for 6d. Additional 6- benzothiazolamine (39mg, 0.29mmol) was added twice to the reaction mixture on the third and fifth days. The reaction was cooled to RT, diluted witii methanol (2OmL), saturated sodium bicarbonate solution was added (ImL) and evaporated to dryness under reduced pressure. The residue was triturated with methanolrDCM (1:1) mixture and filtered. The filtrate was evaporated and the crude product was purified by preparative TLC using 25% methanol in DCM to afford a mixture of benzothiazol-6-yl-[5-bromo-2-(l, 2,3,6- ten-ahydropyridiii4-yl)-lH-pyαolo[2,3-έ]pyridin-4-yl]-amine and 5-bromo-4-chloro-2- (l,2,3,6-tetrahydro-pyridin-4-yl)-lH-pyrrolo[2,3-έ]pyridine as beige solid. Benzotliiazol-6- yl-[5-bromo-2-(l,2,3,6-tetraliydropyridin-4-yl)-lif-pyrrolo[2,3-6]pyridin-4-yl]-amine: MS (ES+): m/z 427.79 (100) [MH⁺], HPLC: fe = 2.12 min (ZQ2000, polar_5mm). 5-Bromo-4- chloro-2-(l,2,3,6-tetrahydropyridin-4-yl)-lH-pyrrolo[2,3-&]pyridine MS (ES+): m/z 313.85 (100) [MH⁺], HPLC: t_R = 2.30 min (ZQ2000, polar_5min).

[930] 4-(5-Bromo-4-chloro-lH-pyrrolo[2,3-6]pyridin-2-yl)-3,6-dihydro-2JΪ- pyridine-1-carboxylic acid tert-butyl ester

[931] To a mixture of 5-bromo-4-chloro-2-iodo-lH-ρyrrolo[2,3-δ]pyridine (46mg,

0.12mmol), potassium carbonate (36mg, 0.25mmol), dichlorobis- (triphenylphosphine)palladium (9mg, O.Olmmol) and 4-(4,4,5,5-tetramethyl- [l,3,2]dioxaborolan-2-yl)-3,6-dihydro-2//-pyridine-l-carboxylic acid tert-butyl ester (42mg, 0.13mmol) were added degassed dioxane (4mL) and water (ImL), and the mixture was heated to reflux for 5h. The reaction was evaporated under reduced pressure and the residue was dissolved in DCM and filtered. The DCM filtrate was evaporated and the crude product obtained was purified by chromatography on silica gel [Jones Flashmaster, 20g / 7OmL cartridge, eluting with DCM:methanol 100:0 → 99.5:0.5], yielding the title compound. MS (ES+): m/z 413.84 (100) [MH⁺]; HPLC: /_R = 6.95 min (ZQ2000, nonpolar_15min). [932] 5-Bromo-4-chloro-2-iodo-l#-pyrrolo[2,3-£]pyridine

[933] To a solution of a 4:6 mixture of l-benzenesulfonyl-5-bromo-4-chloro-2- iodo-lH-pyrrolo[2,3-6]pyridine and 5-bromo-4-chloro-2-iodo-l-(2-iodobenzenesulfonyl)-l//- pyrrolo[2,3 -^pyridine (lOOmg, 0.178mmol) in THF (4mL) was added 3N NaOH in methanol (ImL), and the mixture was stirred at RT for 30min. The reaction was quenched with saturated ammonium chloride solution (2mL), water (5mL) was added, and the mixture was filtered. The precipitate obtained was washed with water (3x1 OmL) followed by hexane (3 x 1OmL) and dried under vacuum to yield the title compound as white solid. ¹H NMR (400 MHz, CD₃OD): δ = 8.21 (s, IH), 6.74 (s, IH); MS (ES+): m/z 358.75 (100) [MH⁺]; HPLC: /_R = 5.68 min (ZQ2000, nonpolar_15min). In vitro activity

[934] All kinases described in the assays below were recombinant and generated at

Upstate (Dundee, UK) except for the KDR assay. Assays were run within 15μM of the apparent Km for ATP where determined, or at lOOμM ATP. For each enzyme, IU activity is defined as the incorporation of lnmol phosphate into the appropriate substrate for a given kinase per minute at 3O⁰C with a final ATP concentration of lOOμM. [935] Assay ATP concentrations for individual kinases are included in the text.

[936] AbI (human) - 45μM ATP: In a final reaction volume of 25μL, AbI (h) (5-

1OmU) is incubated with 8mM MOPS pH 7.0, 0.2mM EDTA, 50μM EAIYAAPFAKKK, 1OmM MgAcetate and [γ-33P-ATP] (specific activity approx. 500cpnα/pmol, concentration as required). The reaction is initiated by the addition of themgATP mix. After incubation for 40min at rt, the reaction is stopped by the addition of 5μL of a 3% phosphoric acid solution. Then, lOμL of the reaction is spotted onto a P30 filtermat and washed three times for 5min in 75mM phosphoric acid and once in methanol prior to drying and scintillation counting. [937] Aurora-A (human) - 15μM ATP: In a final reaction volume of 25μL, Aurora-

A (h) (5-1OmU) is incubated with 8mM MOPS pH 7.0, 0.2mM EDTA, 200μM LRRASLG (Kemptide), 1OmM MgAcetate and [γ-33P-ATP] (specific activity approx. 500cpm/ρmol, concentration as required). The reaction is initiated by the addition of themgATP mix. After incubation for 40min at rt, the reaction is stopped by the addition of 5μL of a 3% phosphoric acid solution. lOμL of the reaction is then spotted onto a P30 filtermat and washed three times for 5min in 5OmM phosphoric acid and once in methanol prior to drying and scintillation counting.

[938] BIk (mouse) - 120μM ATP: In a final reaction volume of 25μL, BIk (m) (5-

1OmU) is incubated with 5OmM Tris pH 7.5, 0.ImM EGTA, 0.1mMNa3VO4, 0.1% β- mercaptoethanol, O.lmg/mL poly(Glu, Tyr) 4:1, 1OmM MgAcetate and [γ-33P-ATP] (specific activity approx. 500cpm/pmol, concentration as required). The reaction is initiated by the addition of themgATP mix. After incubation for 40min at rt, the reaction is stopped by the addition of 5μL of a 3% phosphoric acid solution. 10μL of the reaction is then spotted onto a Filtermat A and washed three times for 5min in 75mM phosphoric acid and once in methanol prior to drying and scintillation counting.

[939] Bmx (human) - 45 μM ATP: In a final reaction volume of 25 μL, Bmx (h) (5-

1OmU) is incubated with 8mM MOPS pH 7.0, 0.2mM EDTA, 0. lmg/ml poly(Glu, Tyr) 4: 1 , 1OmM MgAcetate and [γ-33P-ATP] (specific activity approx. 500cpm/pmol, concentration as required). The reaction is initiated by the addition of themgATP mix. After incubation for 40min at rt, the reaction is stopped by the addition of 5μL of a 3% phosphoric acid solution. lOμL of the reaction is then spotted onto a Filtermat A and washed three times for 5min in 75mM phosphoric acid and once in methanol prior to drying and scintillation counting. [940] CaMKII (rat) - 15μM ATP: In a final reaction volume of 25μL, CaMKII (r)

(5-1OmU) is incubated with 4OmM HEPES pH 7.4, 5mM CaC12, 30μg/mI calmodulin, 30μM KKLNRTLSVA, 1OmM MgAcetate and [γ-33P-ATP] (specific activity approx. 500cpm/pmol, concentration as required). The reaction is initiated by the addition of themgATP mix. After incubation for 40min at rt, the reaction is stopped by the addition of 5μL of a 3% phosphoric acid solution. lOμL of the reaction is then spotted onto a P30 filtermat and washed three times for 5min in 75mM phosphoric acid and once in methanol prior to drying and scintillation counting.

[941] c-RAF (human) - 45 μM ATP: In a final reaction volume of 25μL, c-RAF (h)

(5-1OmU) is incubated with 25mM Tris pH 7.5, 0.02mM EGTA, 0.66mg/mL myelin basic protein, 1OmM MgAcetate and [γ-33P-ATP] (specific activity approx. 500cpm/pmol, concentration as required). The reaction is initiated by the addition of themgATP mix. After incubation for 40min at rt, the reaction is stopped by the addition of 5μL of a 3% phosphoric acid solution. lOμL of the reaction is then spotted onto a P30 filtermat and washed three times for 5min in 75mM phosphoric acid and once in methanol prior to drying and scintillation counting.

[942] cSRC (human) - 200μM ATP: In a final reaction volume of 25μL, cSRC (h)

(5-1OmU) is incubated with 8mM MOPS pH 7.0, 0.2mM EDTA, 250μM KVEKIGEGTYGWYK (Cdc2 peptide), 1OmM MgAcetate and [γ-33P-ATP] (specific activity approx. 500cpm/pmol, concentration as required). The reaction is initiated by the addition of themgATP mix. After incubation for 40min at rt, the reaction is stopped by the addition of 5μL of a 3% phosphoric acid solution. lOμl of the reaction is then spotted onto a P30 filtermat and washed three times for 5min in 75mM phosphoric acid and once in methanol prior to drying and scintillation counting. [943] EGFR (human) - 1 OμM ATP: In a final reaction volume of 25 μL, EGFR (h)

(5-1OmU) is incubated with 8mM MOPS pH 7.0, 0.2mM EDTA, 1OmM MnC12, 0.lmg/mL poly(Glu, Tyr) 4:1, 1OmM MgAcetate and [γ-33P-ATP] (specific activity approx. 500cpm/pmol, concentration as required), The reaction is initiated by the addition of themgATP mix. After incubation for 40min at rt, the reaction is stopped by the addition of 5μL of a 3% phosphoric acid solution. lOμL of the reaction is then spotted onto a Filtermat A and washed three times for 5min in 75mM phosphoric acid and once in methanol prior to drying and scintillation counting.

[944] FGFR3 (human) - 15μM ATP: In a final reaction volume of 25 μL, FGFR3

(h) (5-1OmU) is incubated with 8mM MOPS pH 7.0, 0.2mM EDTA, O.lmg/mL poly(Glu, Tyr) 4:1, 1OmM MnC12, 1OmM MgAcetate and [γ-33P-ATP] (specific activity approx. 500cpm/pmol, concentration as required). The reaction is initiated by the addition of themgATP mix. After incubation for 40min at rt, the reaction is stopped by the addition of 5μL of a 3% phosphoric acid solution. lOμL of the reaction is then spotted onto a Filtermat A and washed three times for 5min in 75 mM phosphoric acid and once in methanol prior to drying and scintillation counting.

[945] Flt3 (human) - 200μM ATP: In a final reaction volume of 25μL Flt3 (h) (5- lOmU) is incubated with 8mM MOPS pH 7.0, 0.2mM EDTA, 50μM EAIYAAPFAKKK, 1OmM MgAcetate and [γ-33P-ATP] (specific activity approx. 500cpm/pmol, concentration as required). The reaction is initiated by the addition of themgATP mix. After incubation for 40min at rt, the reaction is stopped by the addition of 5μL of a 3% phosphoric acid solution. lOμL of the reaction is then spotted onto a P30 filtermat and washed three times for 5min in 75mM phosphoric acid and once in methanol prior to drying and scintillation counting. [946] GSK3β(human) - 15μM ATP: In a final reaction volume of 25μL, GSK3β(h)

(5-1OmU) is incubated with 8mM MOPS pH 7.0, 0.2mM EDTA, 20μM YRRAAVPPSPSLSRHSSPHQS(p)EDEEE (phospho GS2 peptide), 1OmM MgAcetate and [γ-33P-ATP] (specific activity approx. 500cpm/pmol, concentration as required). The reaction is initiated by the addition of themgATP mix. After incubation for 40min at rt, the reaction is stopped by the addition of 5μL of a 3% phosphoric acid solution. lOμL of the reaction is then spotted onto a P30 filtermat and washed three times for 5min in 5OmM phosphoric acid and once in methanol prior to drying and scintillation counting. [947] Lck (human) - 90μM ATP: In a final reaction volume of 25 μL, Lck (h) (5-

1OmU) is incubated with 5OmM Tris pH 7.5, O.lmM EGTA, O.lmM Na3VO4, 250μM KVEKIGEGTYGWYK (Cdc2 peptide), 1OmM MgAcetate and [γ-33P-ATP] (specific activity approx. 500cpm/pmol, concentration as required). The reaction is initiated by the addition of themgATP mix. After incubation for 40min at rt, the reaction is stopped by the addition of 5μL of a 3% phosphoric acid solution. lOμL of the reaction is then spotted onto a P30 filtermat and washed three times for 5min in 75mM phosphoric acid and once in methanol prior to drying and scintillation counting.

[948] MEKl (human) - lOμM ATP: In a final reaction volume of 25 μL, MEKl (h)

(l-5mU) is incubated with 5OmM Tris pH 7.5, 0.2mM EGTA, 0.1% /?-mercaptoethanol, 0.01% Brij-35, lμM inactive MAPK2 (m), 1OmM MgAcetate and cold ATP (concentration as required). The reaction is initiated by the addition of themgATP. After incubation for 40min at rt, 5μL of this incubation mix is used to initiate a MAPK2 (m) assay. In a final reaction volume of 25μL, MAPK2 (h) (5-1OmU) is incubated with 25mM Tris pH 7.5, 0.02mM EGTA, 0.33mg/mL myelin basic protein, 1OmM MgAcetate and [γ-33P-ATP] (specific activity approx. 500cpm/pmol, concentration as required). The reaction is initiated by the addition of themgATP mix. After incubation for 40min at rt, the reaction is stopped by the addition of 5μL of a 3% phosphoric acid solution. lOμL of the reaction is then spotted onto a P30 filtermat and washed three times for 5min in 75mM phosphoric acid and once in methanol prior to drying and scintillation counting.

[949] PDKl (human) - lOμM ATP: In a final reaction volume of 25μL, PDKl (h)

(5-1OmU) is incubated with 5OmM Tris pH 7.5, lOOμM

KTFCGTPEYLAPEVRREPRILSEEEQEMFRDFDYIADWC (PDKtide), 0.1% β- mercaptoethanol, 1OmM MgAcetate and [γ-33P-ATP] (specific activity approx. 500cpm/pmol, concentration as required). The reaction is initiated by the addition of themgATP mix. After incubation for 40min at rt, the reaction is stopped by the addition of 5μL of a 3% phosphoric acid solution. lOμL of the reaction is then spotted onto a P30 filtermat and washed three times for 5min in 75mM phosphoric acid and once in methanol prior to drying and scintillation counting.

[950] PRK2 (human) - 15μM ATP: In a final reaction volume of 25μL, PRK2 (h)

(5-10 mU) is incubated with 5OmM Tris pH 7.5, 0.lmM EGTA, 0.1% /3-mercaptoethanol, 30μM AKRRRLSSLRA, 10 mM MgAcetate and [γ-33P-ATP] (specific activity approx. 500cpm/pmol, concentration as required). The reaction is initiated by the addition of themgATP mix. After incubation for 40min at rt, the reaction is stopped by the addition of 5μL of a 3% phosphoric acid solution. lOμL of the reaction is then spotted onto a P30 filtermat and washed three times for 5min in 75mM phosphoric acid and once in methanol prior to drying and scintillation counting.

[951] Ret (human) - 70μM ATP: In a final reaction volume of 25μL, Ret (h) (5-

1OmU) is incubated with 8mM MOPS pH 7.0, 0.2mM EDTA, 0.25mM KKKSPGEYVNIEFG, 1OmM MgAcetate and [γ-33P-ATP] (specific activity approx. 500cpm/pmol, concentration as required). The reaction is initiated by the addition of themgATP mix. After incubation for 40min at rt, the reaction is stopped by the addition of 5μL of a 3% phosphoric acid solution. lOμL of the reaction is then spotted onto a P30 filtermat and washed three times for 5min in 75mM phosphoric acid and once in methanol prior to drying and scintillation counting.

[952] p70S6K (human) - 15μM ATP: In a final reaction volume of 25μL, p70S6K

(h) (5-1OmU) is incubated with 8mM MOPS pH 7.0, 0.2mM EDTA, lOOμM KKRNRTLTV, lOmM MgAcetate and [γ-33P-ATP] (specific activity approx. 500cpm/pmol, concentration as required). The reaction is initiated by the addition of themgATP mix. After incubation for 40min at rt, the reaction is stopped by the addition of 5μL of a 3% phosphoric acid solution. lOμL of the reaction is then spotted onto a P30 filtermat and washed three times for 5min in 75mM phosphoric acid and once in methanol prior to drying and scintillation counting. [953] SGK (human) - 90μM ATP: In a final reaction volume of 25 μL, SGK (h) (5-

1OmU) is incubated with δmM MOPS pH 7.0, 0.2mM EDTA, 30μM GRPRTSSFAEGKK, 1OmM MgAcetate and [γ-33P-ATP] (specific activity approx. 500cpm/pmol, concentration as required). The reaction is initiated by the addition of themgATP mix. After incubation for 40min at rt, the reaction is stopped by the addition of 5μL of a 3% phosphoric acid solution. lOμL of the reaction is then spotted onto a P30 filtermat and washed three times for 5min in 75mM phosphoric acid and once in methanol prior to drying and scintillation counting. [954] Tie2 (human) - 200μM ATP: In a final reaction volume of 25μL, Tie2 (h) (5-

1OmU) is incubated with 8mM MOPS pH 7.0, 0.2mM EDTA, 0.5mM MnC12, 0.lmg/mL poly(Glu, Tyr) 4:1, 1OmM MgAcetate and [γ-33P-ATP] (specific activity approx. 500cpm/pmol, concentration as required). The reaction is initiated by the addition of themgATP mix. After incubation for 40min at rt, the reaction is stopped by the addition of 5μL of a 3% phosphoric acid solution. lOμL of the reaction is then spotted onto a Filtermat A and washed three times for 5min in 75mM phosphoric acid and once in methanol prior to drying and scintillation counting.

[955] KDR (human) - 18μM ATP: 96-well plates are coated with 0.5μg/75μL/well poly(Glu, Tyr) over night at 37⁰C. 50μL per well of 5OmM Hepes, pH7.4, 125mM NaCl, 24mM MgC12, and 18μM ATP ± compounds are added. The reaction is initiated by the addition of 30μL (5ng) KDR (Proqinase) diluted in assay buffer. After incubation for 30min at rt, the plates are washed and phosphor Tyr detected using pY-20 HRP conjugated antibody with subsequent development using ABTS reagent (KPL) and detection by absorbance at 405nm.

[956] The EXAMPLES 1-81, except for EXAMPLES 2, 3, 4, 8, 11-14, 21, 22,

24, 32, 34, 78, and 79 - for which limited assay results are available - inhibit at least two of the AbI, Aurora-A, BIk, c-Raf, cSRC, Src, PRK2, FGFR3, Flt3, Lck, Mekl, PDK-I, GSKS₁S, EGFR, p70S6K, BMX, SGK, CaMKII, Tie-2, Ret, and KDR kinases at an IC₅₀ of greater than 50% inhibition at lOμM to 14nM. It is advantageous that the measured IC₅₀ be lower than lOμM. It is still more advantageous for the IC₅₀ to be lower than 5μM. It is even more advantageous for the IC₅₀ to be lower than 0.5μM. It is yet more advantageous for the IC₅₀ to be lower than 0.05μM.

[957] Someone skilled in the art will appreciate that other assay formats may be used in place of those described above. For example, AlphaScreen (Amplified Luminescent Proximity Homogeneous Assay) technology was used with the kinases described below. Assay ATP concentrations for individual kinases are included in the text. [958] KDR (human) - lOOμM ATP: 9μL of the reaction mix containing ATP at the desired concentration, biotinylated poly(Glu,Tyr) (84ng/mL) and 0.334 mM vanadate in assay buffer (5OmM HEPES (pH = 7.4), 12.5mM MgCl₂ and 1% glycerol) are added to a well of a 384 well plate along with lμL of compound (or vehicle control, usually DMSO). DMSO concentration is controlled at a concentration of 1%. KDR is diluted to the optimized concentration (optimized on a lot-by-lot basis) in an enzyme diluent buffer (5OmM HEPES pH = 7.4, 12.5 mM MgCl₂ and 1% glycerol, 0.03% Brij35 and 0.3mM EGTA). 5μL of this solution are then added to the well, and the complete reaction mixture is incubated for 60min at RT. In subdued light, 5μL of PT66 donor and acceptor beads (diluted 1:200 from manufacturers provision in a 25mM Tris HCl (pH = 7.5), 20OmM NaCl, 10OmM EDTA, 0.3% BSA buffer) are added to the wells. The plates are then incubated for 4h and read on an AlphaQuest plate reader.

[959] IGF-IR (human) - lOOμM ATP: To a well of a 384 well plate are added 9μL of the reaction mix containing ATP at the desired concentration, biotinylated poly(Glu,Tyr) (84ng/mL) and 0.334mM vanadate in assay buffer (5OmM HEPES (pH = 7.4), 12.5mM MgCl₂ and 1 % glycerol) along with 1 μL of compound (or vehicle control, usually DMSO) . DMSO concentration is controlled at a concentration of 1%. IGF-IR is diluted to the optimized concentration (optimized on a lot-by-lot basis) in an enzyme diluent buffer (5OmM HEPES pH = 7.4, 12.5mM MgCl₂ and 1% glycerol, 0.03% Brij35, 0.3mM EGTA, 6mM DTT, and 0.003% BSA). 5μL of this solution are then added to the well, and the complete reaction mixture is incubated for 60min at RT. In subdued light, 5μL of PT66 donor and acceptor beads (diluted 1 :200 from manufacturer's provision in a 25mM Tris HCl (pH = 7.5), 20OmM NaCl, 10OmM EDTA, 0.3% BSA buffer) are added to the wells. The plates are then incubated for 4h and read on an AlphaQuest plate reader.

[960] Ron (human) - lOOμM ATP: To a well of a 384 well plate are added 9μL of the reaction mix containing ATP at the desired concentration, biotinylated poly(Glu,Tyr) (200ng/mL) and 0.334mM vanadate in assay buffer (5OmM HEPES (pH = 7.4), 12.5mM MgCl₂ and 1% glycerol) along with lμL of compound (or vehicle control, usually DMSO). DMSO concentration is controlled at a concentration of 1%. Ron is diluted to the optimized concentration (optimized on a lot-by-lot basis) in an enzyme diluent buffer (5OmM HEPES pH = 7.4, 12.5mM MgCl₂ and 1% glycerol, 0.03% Brij35, 0.3mM EGTA, ImM DTT, and 0.003% BSA). 5μL of this solution are then added to the well, and the complete reaction mixture is incubated for 60min at RT. In subdued light, 5μL of PT66 donor and acceptor beads (diluted 1 : 160 from manufacturer's provision in a 25mM Tris HCI (pH = 7.5), 20OmM NaCl, 100 mM EDTA, 0.3% BSA buffer) are added to the wells. The plates are then incubated for 4h and read on an AlphaQuest plate reader.

[961] EGFR (human) - 4μM ATP: To a well of a 384 well plate are added 1 μL of compound (or vehicle control, usually DMSO; DMSO concentration is controlled at a concentration of 1%), followed by 9μL of the reaction mix (ATP, at the desired concentration, is added diluted in assay buffer (5OmM HEPES (pH = 7.4), 12.5mM MgCl₂ and 1% glycerol), containing 69.4mM NaCl, biotinylated poly(Glu,Tyr) (84.5ng/mL) and 0.334 mM vanadate). EGFR is diluted to the optimized concentration (optimized on a lot-by-lot basis) in an enzyme diluent buffer (5OmM HEPES pH = 7.4, 12.5 mM MgCl₂ and 1% glycerol, 0.3% Brij35 and 0.3mM EGTA) and Stablecoat (SurModics), and DTT is also added for a concentration of 3mM. 5μL of this solution are then added to the well, and the complete reaction mixture is incubated for 20min at RT. In subdued light, 5 μl of PT66 donor and acceptor beads (diluted 1 :200 from manufacturers provision in a 25 mM Tris HCl (pH = 7.5), 200 mM NaCl, 100 mM EDTA, 0.3% BSA buffer) are added to the wells. The plates are then incubated for 4h and read on an AlphaQuest plate reader.

[962] EGFR (human) - lOOμM ATP: To awell of a 384 well plate are added lμL of compound (or vehicle control, usually DMSO; DMSO concentration is controlled at a concentration of 1%), followed by 9μL of the reaction mix (ATP, at the desired concentration, is added diluted in assay buffer (5OmM HEPES (pH = 7.4), 12.5mM MgCl₂ and 1% glycerol), containing 69.4mM NaCl, biotinylated poIy(Glu,Tyr) (84.5ng/mL) and 0.334mM vanadate). EGFR is diluted to the optimized concentration (optimized on a lot-by-lot basis) in an enzyme diluent buffer (5OmM HEPES pH = 7.4, 12.5 mM MgCl₂ and 1% glycerol, 0.3% Brij35 and 0.3mM EGTA) and Stablecoat (SurModics), and DTT is also added for a concentration of 3mM. 5μL of this solution are then added to the well, and the complete reaction mixture is incubated for 60min at RT. In subdued light, 5μL of PT66 donor and acceptor beads (diluted 1:200 from manufacturer's provision in a 25mM Tris HCl (pH = 7.5), 20OmM NaCl, 10OmM EDTA, 0.3% BSA buffer) are added to the wells. The plates are then incubated for 4h and read on an AlphaQuest plate reader.

[963] PDK- 1 (human) - 1 OOμM ATP: To a well of a 384 well plate are added 1 μL of compound (or vehicle control, usually DMSO; DMSO concentration is controlled at a concentration of 1%), followed by 9μL of the reaction mix (ATP, at the desired concentration, is added diluted in assay buffer (5OmM Tris pH = 7.4, 15mM MgCl₂, O.lmg/mL Bovine gamma globulin, 2mM DTT) containing biotinylated peptide substrate (83.5nM)). PDK-I (obtained from Upstate, 200ng/μL) is diluted 1 :25000 in an enzyme diluent buffer (5OmM Tris pH = 7.4, 15mM MgCl₂, 0.lmg/mL Bovine gamma globulin, 2mM DTT). 5μL of this solution are then added to the well, and the complete reaction mixture is incubated for 2h at RT protected from light. 2.5μL/well of stop buffer (20OmM EDTA in 2OmM Tris / 200 nM NaCl) are added, and the mixture is incubated for Ih at RT protected from light. 2.5 μl/well of antibody/bead complex (antibody diluted 1:1250, donor and acceptor beads diluted 1:200 from manufacturer's provision) are added. The plates are then incubated for 2h at RT protected from light and read on an AlphaQuest plate reader.

[964] PDK-I (human) - 4.5μM ATP: Same procedure, except for the different

ATP concentration.

[965] The EXAMPLES 82-301, except for EXAMPLES 104, 189, 225, 228, 229,

231, 234, 238, 239, 241, 243, 244, 253, 263, 270, 271, 275, 282, 285, 288, 297, 298, and 299 - for which limited assay results are available - inhibit at least two of the IGF-IR, PDK-I, KDR, EGFR, and Ron kinases at greater than 50% inhibition at lOμM. It is advantageous that the measured ICso be lower than lOμM. It is still more advantageous for the IC₅₀ to be lower than 5μM. It is even more advantageous for the IC₅₀ to be lower than 0.5μM. It is yet more advantageous for the IC₅₀ to be lower than 0. lμM.

Claims

WHAT IS CLAIMED IS:

1. A compound represented by Formula I:

(I) or a pharmaceutically acceptable salt thereof, wherein

X is N or C-CN; o < N— —f^~\— __N ^{/^Λ} _N_ __/ \,_

Cy is V-' , ^^ , ^ , \=/

Z is hetaryl, -Ci-βalkyl-O-Ci-βalkyl-, -Co-salkyl-φeterocyclyl), -C₀.,salkyl-(hetaryl), - C(O)-C₀.₆aIkyI, -C(0)-Co.₆alkyl-0-Co.₆alkyl, -C(O)-C₀.salkyl-O-C,.₆alkyl-O-C₀.₆alkyl, - C(0)-C₀.₆alkyl-N(Co.₆alkyl)(Co.₆alkyl), -C(0)-Co.₆alkyl-(heterocyclyl), -C(0)-C₀.₆allcyl- (heterocyclyl)-C(O)-C₀._fialkyl, -C(O)-C₀.₆alkyl- (hetaryl), -S(O)₂-C₀.₆alkyl, -S(O)₂-N(C₀. ₆alkyl)(C₀.₆alkyl), or -S(0)₂-(hetaryl), wherein any of the alkyl, heterocyclyl, or hetaryl optionally is substituted with 1-6 independent halo, OH, -Co-βalkyl-O-Co-βalkyl, -C₀.₆alkyl- N(C₀.₆alkyl)(Co.₆alkyl), -C(0)-Co.₆alkyl-N(Co.₆alkyl)(Co.₆alkyl), -C(0)-Co.₆alkyl- (heterocyclyl), or -C₀.salkyl;

C₂._βalkyl — N N— C₂._βalkyl— N— C_Malkyl V_7 I C_Malkyl

λ CMalkyl — N O

in which tlie wavy bond is the point of attachment, and wherein the piperazine or morpholine moieties are optionally substituted with 1-6 independent Q«alkyl groups; Y is -C(Co.6alkyl)(Co.₆a]kyl)-, -N(C₀.₆alkyl)-, -N(C_Ma]kyl)-C_Ma]kyl-, O, S, >N-C₂. ₆alkyl-N-(C₀.6alkyl)(Co-₆alkyl), >N-C₂.₆alkyl-O-C₀.₆alkyl, >N-C₁.₆alkyl-C(O)-NH-C₀.₆alkyl, or >N-C₂.₆alkyl-N-C(O)-C₁.₆alkyl; and

Rl is aryl, hetaryl, or heterocyclyl, optionally substituted with 1-6 independent halo, -CN, -OH, -Co_₆alkyl, -C^ocycloalkyl, -haloC,.₆alkyl, -C₂._fialkynyl, -N(C₀._βalkyl)(C₀-₆alkyl), - C(0)-Co-6alkyl-N(Co-6alkyl)(Co.₆alkyl), -C(0)-Co.6alkyl-(heterocyclyl), -C].₆alkyl-C(O)-C₀- ₆alkyl-N(Co-6alkyl)(Co.6alkyl) -0-Co.₆alkyl-(heterocyclyl),

-Co-ealkyl- N(Co.₆alkyl)(C_o.₆alkyl), -O-C₀.₆alkyl-(hetaryl)_; -S(O)₂-N(C₀._salkyl)(C₀-₆alkyl), aryl, hetaryl, or heterocyclyl substituents, or substituted with an oxo (=0) using a bond from the aryl, hetaryl, or heterocyclyl ring, wherein any of the substituents optionally is substituted with 1-6 independent halo, CN, OH, -Co-βalkyl-O-Co-βalkyl, -Co-₆alkyl-N(C_o.₆alkyl)(Co.₆alkyl), - C(0)-Co.₆alkyl-N(Co-₆alkyl)(Co.₆alkyl), -C(O)-C₀.₆alkyl-(heterocyclyl), or C₀.₆alkyl.

2. The compound according to claim 1, or a stereoisomer, or a pharmaceutically

acceptable salt thereof, wherein Cy is -fΛ-

3. The compound according to claim 1, or a stereoisomer, or a pharmaceutically acceptable salt thereof, wherein Rl is aryl optionally substituted with halo, -CN, -OH, -C₀. βalkyl, -haloC,.₆alkyl, -C₂.₆alkynyl, -N(C₀.6alkyl)(C₀._salkyl), -C(0)-C₀.6alkyl-N(Co-₆alkyl)(C₀. ₆alkyl), -O-C₀.₆alkyl-(heterocyclyl), -O-C₀-₆alkyl-(hetaryl), -S(O)₂-N(C₀.₆all<yl)(C₀.₆alkyl), aryl, hetaryl, or heterocyclyl substituents, or substituted with an oxo (=0) using a bond from the aryl ring, wherein any of the substituents optionally is substituted with 1-6 independent halo or C₀.₆alkyl.

4. The compound according to claim 1, or a stereoisomer, or a pharmaceutically acceptable salt thereof, wherein Rl is aryl optionally substituted with 1-6 independent halo, -CN, -OH, -C₀.₆alkyl, -Cs-iocycloalkyl, -haloC^alkyl, -C₂.₆alkynyl, -N(C₀.₆alkyl)(Co-₆alkyl), - C(0)-Co-₆alkyl-N(C₀._βalkyl)(C₀.₆alkyl), -C(0)-Co.₆alkyl-(heterocyclyl), -C,.₆alkyl-C(0)-Co. ₆alkyl-N(Co.₆alkyl)(Co_-6alkyl) -0-Co.₆alkyl-(heterocyclyl), -Co.₆alkyl-0-Co.₆alkyl, -Co.₆alkyl- N(Co.₆alkyl)(Co.₆alkyl), -O-C₀.₆alkyl-(hetaryl), -S(0)₂-N(Co.₆alkyl)(Co.₆alkyl), aryl, hetaryl, or heterocyclyl substituents, or substituted with an oxo (=0) using a bond from the aryl, hetaryl, or heterocyclyl ring, wherein any of the substituents optionally is substituted with 1-6 independent halo, CN, OH, -Co-ealkyl-O-Co-βalkyl, -Co.₆alkyl-N(C_o.₆alkyl)(Co-₆alkyl), - C(0)-Co-₆alkyl-N(Co-₆alkyl)(Co.₆alkyl), -C(O)-C₀.₆alkyl-(heterocyclyl), or C₀.₆alkyl.

5. The compound according to claim 1, or a stereoisomer, or a pharmaceutically acceptable salt thereof, wherein Rl is hetaryl optionally substituted with halo, -CN, -OH, -C₀. ₆alkyl, -haloC₁.₆alkyl, -C₂.₆alkynyl, -N(C_o.₆alkyl)(Co.₆alkyl), -C(O)-C₀.₆alkyl-N(C₀.₆alkyl)(C₀. ₆alkyl), -O-C₀.₆alkyl-(heterocyclyl), -O-C₀.₆alkyl-(hetaryl), -S(O)₂-N(C₀.₆alkyl)(C₀.₆alkyl), aryl, hetaryl, or heterocyclyl substituents, or substituted with an oxo (=0) using a bond from the hetaryl ring, wherein any of the substituents optionally is substituted with 1-6 independent halo or Co-βalkyl.

6. The compound according to claim 1, or a stereoisomer, or a pharmaceutically acceptable salt thereof, wherein Rl is hetaryl optionally substituted with 1-6 independent halo, -CN, -OH, -C₀-₆alkyl, -C₃.₁₀cycloalkyl, -haloC,.₆alkyl, -C₂.₆alkynyl, -N(C₀-₆alkyl)(C₀. ₆alkyl), -C(0)-C₀.₆alkyl-N(C₀.₆alkyl)(Co^alkyl), -C(O)-C₀-₆alkyl-(heterocyclyl), -C,.₆alkyl- C(0)-Co.₆alkyl-N(Co-₆alkyl)(Co.₆alkyl),-0-Co.₆alkyl-(heterocyclyl), -Co.₆alkyl-0-Co^alkyl, -Co.₆alkyl-N(Co.₆alkyl)(Co.₆alkyl), -O-C₀.₆alkyl-(hetaryl), -S(0)₂-N(Co.₆alkyl)(Co.₆alkyl), aryl, hetaryl, or heterocyclyl substituents, or substituted with an oxo (=0) using a bond from the aryl, hetaryl, or heterocyclyl ring, wherein any of the substituents optionally is substituted with 1-6 independent halo, CN, OH, -Co^alkyl-O-Co-ealkyl, -Co.₆alkyl-N(Co-₆alkyl)(C₀-₆alkyl), -C(0)-Co.₆alkyl-N(Co.₆alkyl)(Co.₆alkyl), -C(O)-C₀.₆alkyl-(heterocyclyl), or C₀.₆alkyl.

7. The compound according to claim 1, or a stereoisomer, or a pharmaceutically acceptable salt thereof, wherein Rl is heterocyclyl optionally substituted with halo, -CN, -OH, -C₀.₆alkyl, -haloC_Lβalkyl, -C₂.₆alkynyl, -N(C_o.₆alkyl)(Co.₆alkyl), -C(O)-C₀.₆alkyl-N(C₀. ₆alkyl)(Co.₆alkyl),

-O-C₀-₆alkyl-(hetaryl), -S(O)₂-N(C₀.₆alkyl)(C₀. ₆alkyl), aryl, hetaryl, or heterocyclyl substituents, or substituted with an oxo (=0) using a bond from the heterocyclyl ring, wherein any of the substituents optionally is substituted with 1-6 independent halo or C₀.₆alkyl.

8. The compound according to claim 1, or a stereoisomer, or a pharmaceutically acceptable salt thereof, wherein Rl is heterocyclyl optionally substituted with 1-6 independent halo, -CN, -OH, -C₀.₆alkyl, -C_3-i₀cycloalkyl, -haloQ.ealkyl, -C₂._salkynyl, -N(C₀. ₆alkyl)(Co.₆alkyl), -C(0)-C₀.₆alkyl-N(C₀.₆alkyl)(Co.₆alkyl), -C(O)-C₀.₆alkyl-(heterocyclyl), -C₁. ₆alkyl-C(0)-Co.6alkyl-N(Co.6alkyl)(Co.₆alkyl),-0-Co.₆alkyl-(heterocyclyl), -Co-6alkyl-0-Co- ₆alkyl, -Co.₆alkyl-N(Co-₆alkyl)(Co.₆alkyl), -O-C₀.₆alkyl-(hetaryl), -S(O)₂-N(C₀.6alkyl)(C₀. ₆alkyl), aryl, hetaryl, or heterocyclyl substituents, or substituted with an oxo (=0) using a bond from the aryl, hetaryl, or heterocyclyl ring, wherein any of the substituents optionally is substituted with 1-6 independent halo, CN, OH, -Co-ealkyl-O-Co-βalkyl, -C₀_₆alkyl-N(C₀. ₆alkyl)(Co-₆alkyl), -C(O)-C₀.₆alkyl-N(C₀.₆alkyl)(C₀.₆alkyl), -C(O)-C₀.₆alkyl-(heterocyclyl), or C₀.₆alkyl.

9. The compound according to claim 1, or a stereoisomer, or a pharmaceutically acceptable salt thereof, wherein X is N.

10. The compound according to claim 9, or a stereoisomer, or a pharmaceutically

acceptable salt thereof, wherein Cy is

11. The compound according to claim 9, or a stereoisomer, or a pharmaceutically acceptable salt thereof, wherein Y is -N(Qwalkyl)-.

12. The compound according to claim 1 represented by:

or a stereoisomer, or a pharmaceutically acceptable salt thereof, wherein R2 is -C₀.₆alkyl, -C₂. ₆alkyl-N-(Co.₆alkyl)(Co-₆alkyl),

-C₁.₆alkyl-C(0)-NH-Co.₆alkyl₎ or -C₂. ₆alkyl-N-C(O)-C,.₆alkyl.

13. The compound according to claim 1, represented represented by:

R2_{X /}R1 N wherein is selected from the following table:

or a stereoisomer, or a pharmaceutically acceptable salt thereof.

14. The compound according to claim 1, represented by:

or a stereoisomer, or a pharmaceutically acceptable salt thereof, wherein R2 is -C₀.₆alkyl, -C₂, ₆alkyl-N-(C₀.₆alkyl)(C₀.₆alkyl),

-C,.₆alkyl-C(O)-NH-C₀._fialkyl, or -C₂. ₆alkyl-N-C(O)-Ci.₆alkyl.

15. The compound according to claim 1, represented by:

wherein

is selected from the following table:

- 222 -

or a stereoisomer, or a pharmaceutically acceptable salt thereof.

16. The compound according to claim 1, or a stereoisomer, or a pharmaceutically

acceptable salt thereof, wherein Y-Rl is

17. The compound according to claim 1, or a stereoisomer, or a pharmaceutically acceptable salt thereof, wherein X is C-CN.

18. The compound according to claim 17, or a stereoisomer, or a pharmaceutically

acceptable salt thereof, wherein X is C-CN; and Cy is

19. The compound according to claim 17, or a stereoisomer, or a pharmaceutically acceptable salt thereof, wherein X is C-CN; and Y is -N(Co-βalkyl)-.

20. The compound according to claim 1, or a stereoisomer, or a pharmaceutically acceptable salt thereof, wherein Y is -N(C₀.₆alkyl)-.

21. The compound according to claim 1, or a stereoisomer, or a pharmaceutically acceptable salt thereof, wherein Rl is selected from the following table:

22. The compound according to claim 1, or a stereoisomer, or a pharmaceutically acceptable salt thereof, wherein Z is selected from the following:

23. The compound according to claim 1, or a stereoisomer, or a pharmaceutically acceptable salt thereof, represented by:

NR₁R₂ wherein is selected from the following table:

or a stereoisomer, or a pharmaceutically acceptable salt thereof.

24. The compound according to claim 1 or a pharmaceutically acceptable salt

thereof, wherein Y-Rl is

25. The compound according to claim 1 , represented by

or a stereoisomer, or a pharmaceutically acceptable salt thereof, wherein Z is selected from:

26. A composition comprising a compound according to claim 1, or a stereoisomer, or a pharmaceutically acceptable salt thereof; and an anti-neoplastic, anti-tumor, anti-angiogenic, or chemotherapeutic agent.

27. A composition comprising a compound according to claim 1 , or a or a stereoisomer, pharmaceutically acceptable salt thereof, and a cytotoxic cancer therapeutic agent.

28. A composition comprising a compound according to claim 1, or a stereoisomer, or a pharmaceutically acceptable salt thereof, and an angiogenesis inhibiting cancer therapeutic agent.

29. A compound selected from the following:

or a stereoisomer, or a pharmaceutically acceptable salt thereof.

30. A compound selected from the following:

or a stereoisomer, or a pharmaceutically acceptable salt thereof.

31. A compound selected from

4-[4-(4-Fluoro-3-1hiazol-5-ylphenylamino)-7H-pyrrolo[2,3-rf]pyrimidin-6-yl]-3,6-dihydro- 2/f-ρyridine-l-carboxylic acid tert-butyl ester;

4-f4-(4-Fluoro-3-Mazol-5-ylphenylamino)-7H-pyπ:olo[2,3-^pyrirnidin-6-yl]-3,6-dihydro- 2H-pyridine-l-carboxylic acid tert-butylamide;

4-{4-[4-Fluoro-3-(lH-irnidazol-2-yl)-ρhenylardno]-7H-pyrrolo[2,3-^pyrirmdin-6-yl}-3,6- dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester;

4-{4-[4-Fluoro-3-(lH-iimdazol-2-yl)-phenylamino]-7H-pyrrolo[2,3-(i]pyiimidin-6-yl}-3,6- dihydro-2H-pyridine-l-carboxylic acid tert-butylamide;

4-[4-(4-Fluoro-3-imidazol-l-ylphenylammo)-7H-pyrrolo[2,3-rf]pyrirnidin-6-yl]-3,6-dib.ydro- 2H-pyridine-l-carboxylic acid tert-butyl ester;

4-[4-(4-Fluoro-3-irrddazol-l-ylphenylaiiimo)-7H-pyrrolo[2,3-rf]pyrii'riidin-6-yl]-3,6-dihydro- 2H-pyriditie-l-carboxylic acid tert-butylamide;

4- {4-[4-Fluoro-3 -(4-methylpiρerazin- 1 -yl)-phenylamino] -7H-pyrrolo [2,3 -(f]pyrimidin-6-yl} - 3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester;

4-{4-[4-Fluoro-3-(4-methylpiρerazin-l-yl)-phenylamino]-7H-pyrrolo[2,3-d]pyrimidin-6-yl}- 3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butylamide;

4- {4-[4-Fluoro-3 -(I -methylazetidin-3 -ylmethyl)-phenylarrώio]-7H-pyrrolo[2,3 -cTjpyrimidin- 6-yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester;

4-{4-[4-Fluoro-3-(l-methylazetidin-3-ylmetiiyl)-phenylarmno]-7H-pyrrolo[2,3-^p}τirnidin- 6-yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butylamide;

4-{4-[4-Fluoro-3-(l-inethylazetidin-3-yloxy)-phenylamino]-7H-pyrrolo[2,3-(/lpyrimidin-6- yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester;

4-{4-[4-Fluoro-3-(l-metiiylazetidin-3-yloxy)-phenylammo]-7H-ρyrrolo[2,3-J]pyrimidin-6- yl}-3,6-dilαydro-2H-ρyridine-l-carboxylic acid tert-butyl ester;

4-{4-[4-Fluoro-3-(4-methylpiperazin-l-ylmethyl)-phenylamino]-7H-pyrrolo[2,3-^/]pyrimidin- 6-yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester;

4-{4-[4-Fluoro-3-(4-methylpiperazin-l-ylmethyl)-phenylainino]-7H-pyrrolo[2,3-ιi]pyrirnidin- 6-yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butylamide;

4- {4-[4-Fluoro-3 -(I -methyl- 1 ,2,3 ,6-tetrahydropyridin-4-yl)-phenylamino]-7H-pyrrolo[2,3 - cflpyrimidin-6-yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester; 4-{4-[4-Fluoro-3-(l-methyl-l,2,3,6-tetrahydropyridin-4-yl)-phenylarnino]-7H-pyrrolo[2,3- J]pyrimidin-6-yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl amide; 4-{4-[4-Fluoro-3-(l-methyl-2,5-dihydro-lH-pyrrol-3-yl)-phenylamino]-7H-pyrrolo[2,3- ^]pyrimidin-6-yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester; 4-{4-[4-Fluoro-3-(l-methyl-2,5-dihydro-lH-ρyrrol-3-yl)-phenylamino]-7H-pyτrolo[2,3- ύ(]pyriπiidin-6-yl}-3,6-dihydro-2//^'-pyridine-l-carboxylic acid tert-butyl amide; (5)^-{4-[4-Fluoro-3-(l-metiiylpyrrolidk-3-yl)-phenylamino]-7H-pyrrolo[2,3-6ripyrimidin-6- yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester;

(5)^-{4-[4-Fluoro-3-(l-me1iiylpyrrolidin-3-yl)-phenylamino]-7H-pyrrolo[2,3-<^pyrimidiii-6- yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl amide;

(R)-4-{4-[4-Fluoro-3-(l-metiiylpyrrolidin-3-yl)-phenylainino]-7H-pyrrolo[2,3-rflpyrimidin-6- yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester;

(R)-4-{4-[4-Fluoro-3-(l-methylpyiτolidin-3-yl)-phenylarriino]-7H-pyrrolo[2,3-J]pyrimidin-6- yl}-3,6-dihydro-2H-ρyridine-l-carboxylic acid tert-butyl amide;

{4-[4-(Benzomiazol-6-ylarnino)-7H-pyiτolo[2,3-rf]pyrirriidin-6-yl]-3,6-dihydro-2H-pyridin-l- yl} -(2,2,4-trimethylpiperazin-l -yl)-methanone;

{4-[4-(Benzomiazol-6-ylamino)-7H-pyrrolo[2,3-^pyrimidin-6-yl]-3,6-dib.ydro-2H-pyridin-l- yl}-(2,4,5-trimethylpiperazin-l-yl)-methanone;

{4-[4-(Benzomiazol-6-ylainino)-7H-pyrrolo[2,3-^pyrirnidin-6-yl]-3,6-dihydro-2H-pyridin-l- yl } -(3 ,4,5 -trimethylpiperazin-1 -yl)-methanone;

{4-[4-(Benzothiazol-6-ylanτino)-7H-pyrrolo[2,3-^pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l- yl} -[4-(2,2,2-trifluoroethyl)-piperazin-l -yl]-methanone;

{4-[4-(Benzomiazol-6-ylamino)-7H-pyrrolo[2,3-c/]pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l- yl} -(4-tert-butylpiperazin-l -yl)-methanone;

Benzothiazol-6-yl-[6-(3,6-dihydro-2H41,2]bipyridinyl-4-yl)-7H-pyrrolo[2,3-J]pyrimidin-4- yl] -amine;

Benzothiazol-6-yl-[6-(l-thiazol-2-yl-l,2,3,6-tetrahydropyridrα-4-yl)-7H-pyrrolo[2,3- (^]pyrimidin-4-yl]-amine;

Benzothiazol-6-yl-[6-(l-oxazoI-2-yl-l,2,3,6-tetrahydropyridrn-4-yl)-7H-pyrrolo[2,3- rf]pyrimidin-4-yl] -amine;

4-[4-(3-Phenyl-3H-benzimidazol-5-ylammo)-7H-pyrrolo[2,3-d]pyrimidin-6-yl]-3,6-dihydro- 2H-pyridine-l-carboxylic acid tert-butyl ester;

4-[4-(3-Phenyl-3H-benzimidazol-5-ylamino)-7H-pyrrolo[2,3-£/]pyriimdin-6-yl]-3,6-dihydro- 2H-pyridine-l-carboxylic acid tert-butylamide;

4-{4-[3-(2-Carbamoylphenyl)-3H-benzirnidazol-5-ylamino]-7H-pyrrolo[2,3-ύ?]pyrimidiri-6- yl}-3,6-dihydro-2H-pyriditie-l-carboxylic acid tert-butylamide;

4-{4-[3-(2-Carbamoylphenyl)-3H-benzurύdazol-5-ylaim^'no]-7H-pyrrolo[2,3-^pyrirnidin-6- yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester;

4-{4-[3-(2-Aniinoethyl)-3H-benzimidazol-5-ylamino]-7H-pyrrolo[2,3-d]pyriinidin-6-yl}-3,6- dihydro-2H-pyridine-l-carboxylic acid tert-butylamide; 4-{4-[3-(2-Aminoethyl)-3H-benzimidazol-5-ylamino]-7H-pyrrolo[2,3-(/]pyrimidin-6-yl}-3,6- dihydro-2i7-pyridine- 1-carboxylic acid fert-butyl ester;

4-{4-[3-(2-Dimethylaminoethyl)-3H-benzirnidazol-5-ylainino]-7H-pyrrolo[2,3-^pyrirnidin- 6-yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butylamide;

4-{4-[3-(2-Dimethylaminoethyl)-3H-benzimidazol-5-ylamino]-7H-ρyrrolo[2,3-^pyrirnidin- 6-yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-bvAyl ester;

4-{4-[3-(2-Acetylaminoe1hyl)-3H-benzimidazol-5-ylaimno]-7H-pyπolo[2,3-(flpyrimidin-6- yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butylamide;

4-{4-[3-(2-Acetylarninoe<iιyl)-3H-benzύnidazol-5-ylamino]-7H-pyrrolo[2,3-(flpyrirnidin-6- yl} -3 ,6-dihydro-2H-pyridine- 1-carboxylic acid tert-butyl ester;

4-[4-(Iirddazo[l,2-β]pyridin-6-ylamino)-7H-pyrrolo[2,3-J]pyrimidin-6-yl]-3,6-dihydro-2H- pyridine- 1-carboxylic acid tert-butylamide;

4-[4-(Imidazo[l,2-a]pyridin-6-ylamino)-7H-pyrrolo[2,3-d]pyriinidin-6-yl]-3,6-dihydro-2H- pyridine- 1-carboxylic acid tert-butyl ester;

4-t4-(3-Methylimidazo[l,2-α]pyridin-6-ylarriino)-7H-pyπⁱolo[2,3-^pyriniidin-6-yl]-3,6- diliydro-2H-pyridine- 1-carboxylic acid fert-butylamide;

4-[4-(3-Methylirddazo[l,2-α]pyridin-6-ylarnino)-7H-pyrrolo[2,3-(^pyrimidin-6-yl]-3,6- dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester;

4-[4-(3-Phenylirmdazo[l,2-fl]pyridin-6-ylamino)-7H-pyrrolo[2,3-rfjpyrimidin-6-yl]-3,6- dihydro-2H-pyridine- 1-carboxylic acid tert-butylamide;

4-[4-(3-Phenylirddazo[l,2-α]pyridin-6-ylamirio)-7H-pyrrolo[2,3-d]pyrimidin-6-yl]-3,6- dihydro-2H-pyridine- 1-carboxylic acid ter^-butyl ester;

4-{4-[3-(2-Carbamoylphenyl)-imidazo[l,2-β]pyridin-6-ylarnino]-7H-pyrrolo[2,3- cfjpyrimidin-ό-ylJ-S^-diliydro^H-pyridine-l-carboxylic acid tert-butylamide; 4-{4-[3-(2-CarbamoyIphenyl)-imidazo[l,2-α]pyridin-6-ylamino]-7H-pyrrolo[2,3- rf]pyrimidin-6-yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester; 4-{4-[3-(2-Dimethylaminoethyl)-imidazo[l,2-α]pyridin-6-ylai-nino]-7H-pyrrolo[2,3- d]pyrimidin-6-yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butylamide; 4- {4-[3 -(2-Dimethylaminoethyl)-imidazo[ 1 ,2-α]pyridin-6-ylamino] -7H-pyrrolo[2,3 - ^Ipyrimidm-β-ylJ-S^-diliydro^H-pyridine-l-carboxylic acid /ert-butyl ester; 4-{4-[3-(2-Acetylaminoetliyl)-imidazo[l,2-α]pyridiri-6-ylarriino]-7H-pyrrolo[2,3- rf]pyrimidin-6-yl}-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butylamide; 4-{4-[3-(2-Acetylairύnoetiiyl)-imidazo[l,2-α]pyridin-6-ylarnino]-7H-ρyrrolo[2,3- d]pyrimidin-6-yl}-3,6-diliydro-2H-pyridine-l-carboxylic acid ter^-butyl ester; 4-[4-(3-Dimethylammomethylimdazo[l,2-α]pyridm-6^ 6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butylamide; -[4-(3-Dimethylaminomethylimidazo[ 1 ,2-<z]pyridin-6-ylamino)-7H-pyrrolo[2,3 -cT]pyrimidiii-

6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester; -f4-(7-Aininomethyl-lH-indazol-5-ylamino)-7H-pyrrolo[2,3-^pyrirnidin-6-yl]-3,6-dihydro

2H~pyridine-l -carboxylic acid tert-butylamide;

4-[4-(7-Aminomethyl-lH-indazol-5-ylajmino)-7Hφyrrolo[2,3-d]pyriinidin-6-yl]-3,6-dihydro-

2iϊ-pyridine-l -carboxylic acid tert-butyl ester;

4-[4-(7-Armnomethyl-l-methyl-lH-indazol-5-ylamino)-7H-pyrrolo[2,3-(i]pyrimidin-6-yl]^

3,6-dihydro-2H-pyridine-l -carboxylic acid tert-butylamide;

4-[4-(7-Aminomethyl- 1 -methyl- lH-indazol-5-ylamino)-7H-pyrrolo[2,3 -</]pyrimidin-6-yl]-

3 ,6-dihydro-2i/-pyridine-l -carboxylic acid fø^-butyl ester;

4-[4-(7-DimetJiylarriinome1iiyl-l-methyl-lH-indazol-5-ylairdno)-7H-pyiτolo[2,3-^pyrimidin-

6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid ter^-butylamide;

4-[4-(7-Dimethylarninome1iyl-l-methyl-lH-indazol-5-ylamino)-7H-pyrrolo[2,3-(flpyrirm

6-yl]-3,6-dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester;

4-[4-(7-Dimeώylammomethyl-lH-ώdazol-5-ylamino) dihydro^H-pyridine-l-carboxylic acid tert-butylamide;

4-[4-(7-Dimethylaminomethyl-lH-indazol-5-ylamino)-7H-pyrrolo[2,3-(i]pyrimidin-6-yl]-3,6- dihydro-2H-pyridine-l-carboxylic acid ter^-butyl ester;

4-{4-[7-(2-Dimethylaminoethyl)-lH-indazol-5-ylamino]-7H-pyπ-olo[2,3-d]pyrimidiri-6-yl}-

3,6-dihydro-2H-pyridine-l-carboxylic acid ter/-butylamide;

4-{4-[7-(2-Dime1hylanτinoethyl)-lH-indazol-5-ylarrύno]-7H-pyiτolo[2,3-cr]pyrirnidiri-6-yl}-

3,6-dihydro-2H-pyridine-l-carboxylic acid ter^-butyl ester;

4-{4-[7-(2-Dimethylaminoethyl)-l-methyl-lH-indazol-5-ylamino]-7H-pyrrolo[2,3-

(f]pyrimidin-6-yl} -3 ,6-dihydro-2H-pyridine- 1 -carboxylic acid tert-butylamide;

4-{4-[7-(2-Dimetiiylaminoethyl)-l-methyl-lH-indazol-5-ylamino]-7H-pyrrolo[2,3-

(f]pyrimidin-6-yl}-3,6-diliydro-2H-pyridine-l-carboxylic acid tert-butyl ester;

4-[4-(Iimdazo[l,5-α]pyridm-6-ylamino)-7H-pyrrolo[2,3-^pyrimidin-6-yl]-3,6-dihydro-2H- pyridine-1 -carboxylic acid tert-butylamide;

4-[4-(Imidazo[l,5-α]pyridin-6-ylamino)-7H-ρyrrolo[2,3-^pyrirnidin-6-yl]-3,6-dihydro-2H- pyridine-1 -carboxylic acid tert-butyl ester;

4-[4-(3-Methylimidazo[l,5-β]pyridin-6-ylamino)-7H-pyrrolo[2,3-βripyrimidin-6-yl]-3,6- dihydro-2H-pyridine-l -carboxylic acid tert-butylamide;

4-[4-(3-Methyliπudazo[l₎5-β]pyridm-6-ylarnino)-7H-pyrrolo[2,3-d]pyrirnidin-6-yl]-3,6- dihydro-2H-pyridine-l -carboxylic acid tert-butyl ester;

4-[4-(l-Methylimidazo[l₎5-α]pyridm-6-ylamino)-7H-pyrrolo[2,3-rf]pyriiτiidin-6-yl]-3,6- dihydro-2H-pyridine-l -carboxylic acid tert-butylamide; 4-[4-(l-Metliylimidazo[l,5-(2]pyridm-6-ylamino)-7H-pyrrolo[2,3-^pyriinidin-6-yl]-3,6- dihydro-2H-pyridine-l -carboxylic acid tert-butyl ester;

4-[4-(Imidazo[l,5-α]pyridin-7-ylariύno)-7H-pyrrolo[2,3-J]pyriiiύdin-6-yl]-3,6-dihydro-2H- pyridine-1-carboxylic acid fert-butylamide;

4-[4-(Irnidazo[l,5-α]pyridin-7-ylamino)-7H-ρyrrolo[2,3-J]pyrimidin-6-yl]-3,6-dihydro-2H- pyridine-1-carboxylic acid tert-butyl ester; 4-[4-(3-MethylirrMazo[l,5-a]pyridin-7-ylarritoo)-^^ dihydro-2H-pyridine--l -carboxylic acid fert-butylamide;

4-[4-(3-Methylimidazo[l,5-α]pyridin-7-ylamino)-7H-pyπ:olo[2,3-(i]pyrimidin-6-yl]-3,6- dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester;

4-[4-(l-Methylirnidazo[l,5-α]pyridin-7-ylarnino)-7H-pyrrolo[2,3-^pyrimidin-6-yl]-3,6- dihydro-2H-pyridine-l-carboxylic acid tert-butylamide;

4-[4-(l-Methylimidazo[l,5-α]pyridin-7-ylarnino)-7H-pyrrolo[2,3-J]pyrirnidin-6-yl]-3,6- dihydro-2H-pyridine-l-carboxylic acid tert-butyl ester;

4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-ι^p)σimidin-6-yl]-3,6-dihydro-2H-pyridine-l- carboxylic acid (2-hydroxy-l,l-dimethylethyl)-amide;

444-(l-Methyl4H-mdazol-5-ylamino)-7H-pyrrolo[2,3-^pyrirrύdin-6-yl]-3,6-dihydro-2H- pyridine-1 -carboxylic acid (2-hydroxy-l,l-dimethyletriyl)-amide;

4-[4-(Benzo1iiiazol-6-ylamino)-7H-pyπ-olo[2,3-d]pyrimidin-6-yl]-3,6-dihydro-2H-pyridirie-l- carboxylic acid (2-methoxy-l,l-dimethylethyl)-amide;

4-[4-(l-Methyl-lH-indazol-5-ylamino)-7H-pyrrolo[2,3-^pyrirnidin-6-yl]-3,6-dihydro-2H- pyridine-1-carboxylic acid (2-methoxy-l,l-dimethylethyl)-amide;

4-[4-(Benzothiazol-6-ylamino)-7H-pyπ-olo[2,3-(i]pyrimidin-6-yl]-3,6-dihydro-2Z/-pyridine-l- carboxylic acid (2-dirnethylamino-l,l-dimethylethyl)-amide;

4-[4-(l-Methyl-lH-indazol-5-ylarnino)-7H-pyπ-olo[2,3-(i]pyrirnidin-6-yl]-3,6-dihydro-2H- pyridine-1-carboxylic acid (2-dimethylamino-l,l-dimethylethyl)-amide; 4-[4-(Benzothiazol-6-ylamino)-7H-pyrrolo[2,3-cTlpyriiriidin-6-yl]-3,6-dihydro-2H-pyridine-l- carboxylic acid (l,l-dimethyl-2-pyrrolidin-l-ylethyl)-amide;

4-[4-(l-Methyl-lH-indazol-5-ylamino)-7H-pyrrolo[2,3-d]pyrirnidin-6-yl]-3,6-dihydro-2H- pyridine-1-carboxylic acid (l,l-dimethyl-2-pyrrolidin-l-ylethyl)-amide; 4-[4-(Benzolhiazol-6-ylarnino)-7H-pyrrolo[2,3-^pyrimidin-6-yl]-3,6-diliydro-2H-pyridine-l- carboxylic acid (l,l-dimethyl-2-moφholin-4-yletriyl)-amide;

4-[4-(l-Methyl-lH-indazol-5-ylamino)-7H-pyrrolo[2,3-d]pyrimidin-6-yl]-3,6-dihydro-2H- pyridine-1-carboxylic acid (1 ,1 -dimethyl-2-morpholin-4-ylethyl)-amide; 4-[4-(lH-Indol-5-ylamino)-7H-pyrrolo[2,3-^pyrimidin-6-yl]-3,6-dihydro-2H-pyridine-l- carboxylic acid tert-butylamide; 4-[4-(Quinolin-6-ylamino)-7H-pyrrolo[2,3-<^pyriimdin-6-yl]-3,6-dihydro-2H-pyridine-l- carboxylic acid fert-butylamide;

(Hexahydroρyrrolo[l,2-α]pyrazin-2-yl)-{4-[4-(imidazo[l,2-α]pyridin-6-ylamino)-7iϊ- pyrrolop^-cTlpyriniidin-o-ylj-S_jo-dihydro^iY-pyridirL-l-yll-methanone;

(Hexahydroρyrrolo[l,2-α]pyrazin-2-yl)-{4-[4-(3-methyl-3H-benzoimidazol--5-ylamino)-7H- pyrrolo[2,3-cT|pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yl}-metlianone;

(Hexahydroρyrrolo[l,2-fl]pyrazin-2-yl)-{4-[4-(l-methyl-lH-indazol-5-ylamino)-7H- pyrrolo[2,3-^]pyrimidin-6-yl]-3,6-dihydro-2H-pyridin-l-yl}-melhanone;

{4-[4-(Benzothiazol-6-ylarnino)-7H-pyrrolo[2,3-^pyriroidin-6-yl]-3,6-dihydro-2H-pyridin-l- yl}-(hexahydropyrrolo[l,2-α]pyrazin-2-yl)-methanone; or a stereoisomer, or a pharmaceutically acceptable salt thereof.

32. A method of treatment of hyperproliferative disorder comprising a step of administering an effective amount of the compound according to claim 1.

33. The method of claim 32, further comprising the step of administering an anti¬ neoplastic, anti-tumor, anti-angiogenic, or chemotherapeutic agent.

34. The method of claim 32 wherein the hyperproliferative disorder is breast cancer, head cancer, or neck cancer.

35. The method of claim 32 wherein the hyperproliferative disorder is gastrointestinal cancer.

36. The method of claim 32 wherein the hyperproliferative disorder is leukemia.

37. The method of claim 32 wherein the hyperproliferative disorder is ovarian, bronchial, lung, or pancreatic cancer.

38. The method of claim 32 wherein the hyperproliferative disorder is small cell lung or colon cancer.

39. The method of claim 32 wherein the hyperproliferative disorder is sinonasal natural killer/T-cell lymphoma, testicular cancer (seminoma), thyroid carcinoma, malignant melanoma, ovarian carcinoma, adenoid cystic carcinoma, acute myelogenous leukemia (AML), breast carcinoma, pediatric T-cell acute lymphoblastic leukemia, angiosarcoma, anaplastic large cell lymphoma, endometrial carcinoma, or prostate carcinoma.