3-[(1H-PYRAZOL-R-YL)OXY]PYRAZIN-2-AMINE COMPOUNDS AS HPK1 INHIBITOR AND USE THEREOF

Abstract

Disclosed herein is 3-[(1H-pyrazol-4-yl)oxy]pyrazin-2-amine compounds of Formula (I), or a stereoisomer thereof, or a pharmaceutically acceptable salt thereof, and pharmaceutical compositions comprising thereof. Also disclosed is a method of modulating, e.g., inhibiting or treating HPK1 related disorders or diseases including cancer by using the compound disclosed herein

##STR00001##

Claims

1.-17. (canceled)

18. A compound selected from: ##STR00458## ##STR00459## ##STR00460## ##STR00461## or a pharmaceutically acceptable salt thereof.

19. A pharmaceutical composition comprising the compound of claim 18, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable excipient.

20. A method of treating cancer in a subject in need thereof, comprising administering to the subject the compound of claim 18, or a pharmaceutically acceptable salt thereof.

21. The compound of claim 18, wherein the compound is ##STR00462## or a pharmaceutically acceptable salt thereof.

22. The compound of claim 18, wherein the compound is ##STR00463## or a pharmaceutically acceptable salt thereof.

23. The compound of claim 18, wherein the compound is ##STR00464## or a pharmaceutically acceptable salt thereof.

24. The compound of claim 18, wherein the compound ##STR00465## or a pharmaceutically acceptable salt thereof.

25. The compound of claim 18, wherein the compound is ##STR00466## or a pharmaceutically acceptable salt thereof.

26. The compound of claim 18, wherein the compound is ##STR00467## or a pharmaceutically acceptable salt thereof.

27. The compound of claim 18, wherein the compound is ##STR00468## or a pharmaceutically acceptable salt thereof.

28. The compound of claim 18, wherein the compound ##STR00469## or a pharmaceutically acceptable salt thereof.

29. The compound of claim 18, wherein the compound is ##STR00470## or a pharmaceutically acceptable salt thereof.

30. The compound of claim 18, wherein the compound is ##STR00471## or a pharmaceutically acceptable salt thereof.

31. The compound of claim 18, wherein the compound is ##STR00472## or a pharmaceutically acceptable salt thereof.

32. The compound of claim 18, wherein the compound is ##STR00473## or a pharmaceutically acceptable salt thereof.

33. The compound of claim 18, wherein the compound is ##STR00474## or a pharmaceutically acceptable salt thereof.

34. The compound of claim 18, wherein the compound is ##STR00475## or a pharmaceutically acceptable salt thereof.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0097] The following terms have the indicated meaning throughout the specification:

[0098] Unless specifically defined elsewhere in this document, all other technical and scientific terms used herein have the meaning commonly understood by one of ordinary skill in the art to which this invention belongs.

[0099] The following terms have the indicated meanings throughout the specification: As used herein, including the appended claims, the singular forms of words such as a, an, and the, include their corresponding plural references unless the context clearly indicates otherwise.

[0100] The term or is used to mean, and is used interchangeably with, the term and/or unless the context clearly dictates otherwise.

[0101] The term alkyl refers to a hydrocarbon group selected from linear and branched, saturated hydrocarbon groups comprising from 1 to 18, such as from 1 to 12, further such as from 1 to 10, more further such as from 1 to 8, or from 1 to 6, or from 1 to 4, carbon atoms. Examples of alkyl groups comprising from 1 to 6 carbon atoms (i.e., C.sub.J-6 alkyl) include, but not limited to, methyl, ethyl, 1-propyl or n-propyl (n-Pr), 2-propyl or isopropyl (i-Pr), 1-butyl or n-butyl (n-Bu), 2-methyl-1-propyl or isobutyl (i-Bu), 1-methylpropyl or s-butyl (s-Bu), 1,1-dimethylethyl or t-butyl (t-Bu), 1-pentyl, 2-pentyl, 3-pentyl, 2-methyl-2-butyl, 3-methyl-2-butyl, 3-methyl-1-butyl, 2-methyl-1-butyl, 1-hexyl, 2-hexyl, 3-hexyl, 2-methyl-2-pentyl, 3-methyl-2-pentyl, 4-methyl-2-pentyl, 3-methyl-3-pentyl, 2-methyl-3-pentyl, 2,3-dimethyl-2-butyl and 3,3-dimethyl-2-butyl groups.

[0102] The term propyl refers to 1-propyl or n-propyl (n-Pr), 2-propyl or isopropyl (i-Pr).

[0103] The term butyl refers to 1-butyl or n-butyl (n-Bu), 2-methyl-1-propyl or isobutyl (i-Bu), 1-methylpropyl or s-butyl (s-Bu), 1,1-dimethylethyl or t-butyl (t-Bu).

[0104] The term pentyl refers to 1-pentyl, 2-pentyl, 3-pentyl, 2-methyl-2-butyl, 3-methyl-2-butyl, 3-methyl-1-butyl, 2-methyl-1-butyl.

[0105] The term hexyl refers to 1-hexyl, 2-hexyl, 3-hexyl, 2-methyl-2-pentyl, 3-methyl-2-pentyl, 4-methyl-2-pentyl, 3-methyl-3-pentyl, 2-methyl-3-pentyl, 2,3-dimethyl-2-butyl and 3,3-dimethyl-2-butyl.

[0106] The term halogen refers to fluoro (F), chloro (Cl), bromo (Br) and iodo (I).

[0107] The term haloalkyl refers to an alkyl group in which one or more hydrogen is/are replaced by one or more halogen atoms such as fluoro, chloro, bromo, and iodo. Examples of the haloalkyl include haloC.sub.1-8 alkyl, haloC.sub.1-6alkyl or halo C.sub.1-4alkyl, but not limited to CF.sub.3, CH.sub.2Cl, CH.sub.2CF.sub.3, CHCl.sub.2, ?CF.sub.3, and the like.

[0108] The term alkenyl refers to a hydrocarbon group selected from linear and branched hydrocarbon groups comprising at least one C?C double bond and from 2 to 18, such as from 2 to 8, further such as from 2 to 6, carbon atoms. Examples of the alkenyl group, e.g., C.sub.2-6 alkenyl, include, but not limited to ethenyl or vinyl, prop-1-enyl, prop-2-enyl, 2-methylprop-1-enyl, but-1-enyl, but-2-enyl, but-3-enyl, buta-1,3-dienyl, 2-methylbuta-1,3-dienyl, hex-1-enyl, hex-2-enyl, hex-3-enyl, hex-4-enyl, and hexa-1,3-dienyl groups.

[0109] The term alkynyl refers to a hydrocarbon group selected from linear and branched hydrocarbon group, comprising at least one C?C triple bond and from 2 to 18, such as 2 to 8, further such as from 2 to 6, carbon atoms. Examples of the alkynyl group, e.g., C.sub.2-6 alkynyl, include, but not limited to ethynyl, 1-propynyl, 2-propynyl (propargyl), 1-butynyl, 2-butynyl, and 3-butynyl groups.

[0110] The term cycloalkyl refers to a hydrocarbon group selected from saturated cyclic hydrocarbon groups, comprising monocyclic and polycyclic (e.g., bicyclic and tricyclic) groups.

[0111] For example, the cycloalkyl group may comprise from 3 to 12, such as from 3 to 10, further such as 3 to 8, further such as 3 to 6, 3 to 5, or 3 to 4 carbon atoms. Even further for example, the cycloalkyl group may be selected from monocyclic group comprising from 3 to 12, such as from 3 to 10, further such as 3 to 8, 3 to 6 carbon atoms. Examples of the monocyclic cycloalkyl group include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, cyclononyl, cyclodecyl, cycloundecyl, and cyclododecyl groups. In particular, Examples of the saturated monocyclic cycloalkyl group, e.g., C.sub.3-8cycloalkyl, include, but not limited to cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, and cyclooctyl groups. In a preferred embedment, the cycloakyl is a monocyclic ring comprising 3 to 6 carbon atoms (abbreviated as C.sub.3-6 cycloalkyl), including but not limited to, cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl. Examples of the bicyclic cycloalkyl groups include those having from 7 to 12 ring atoms arranged as a fused bicyclic ring selected from [4,4], [4,5]. [5,5], [5,6] and [6,6] ring systems, or as a bridged bicyclic ring selected from bicyclo[2.2.1]heptane, bicyclo[2.2.2]octane, and bicyclo[3.2.2]nonane. Further Examples of the bicyclic cycloalkyl groups include those arranged as a bicyclic ring selected from [5,6] and [6,6] ring systems.

[0112] The term fused cycloalkyl refers to a bicyclic cycloalkyl group as defined herein which is saturated and is formed by two or more rings sharing two adjacent atoms.

[0113] The term bridged cycloalkyl refers to a cyclic structure which contains carbon atoms and is formed by two rings sharing two atoms which are not adjacent to each other. The term 7 to 12 membered bridged cycloalkyl refers to a cyclic structure which contains 7 to 12 carbon atoms and is formed by two rings sharing two atoms which are not adjacent to each other.

[0114] The term cycloalkenyl refers to non-aromatic cyclic alkyl groups of from 3 to 10 carbon atoms having single or multiple rings and having at least one double bond and preferably from 1 to 2 double bonds. In one embodiment, the cycloalkenyl is cyclopentenyl or cyclohexenyl, 1-cyclopent-1-enyl, 1-cyclopent-2-enyl, 1-cyclopent-3-enyl, 1-cyclohex-1-enyl, 1-cyclohex-2-enyl, 1-cyclohex-3-enyl, cyclohexadienyl, preferably cyclohexenyl. The term fused cycloalkenyl refers to a bicyclic cycloalkyl group as defined herein which contain at least one double bond and is formed by two or more rings sharing two adjacent atoms.

[0115] The term cycloalkynyl refers to non-aromatic cycloalkyl groups of from 5 to 10 carbon atoms having single or multiple rings and having at least one triple bond.

[0116] The term fused cycloalkynyl refers to a bicyclic cycloalkyl group as defined herein which contains at least one triple bond and is formed by two or more rings sharing two adjacent atoms.

[0117] Examples of fused cycloalkyl, fused cycloalkenyl, or fused cycloalkynyl include but are not limited to bicyclo[1.1.01]butyl, bicyclo[2.1.0]pentyl, bicyclo[3.1.0]hexyl, bicyclo[4.1.0]heptyl, bicyclo[3.3.0]octyl, bicyclo[4.2.0]octyl, decalin, as well as benzo 3 to 8 membered cycloalkyl, benzo C.sub.4-6 cycloalkenyl, 2,3-dihydro-1H-indenyl, 1H-indenyl, 1, 2, 3,4-tetralyl, 1,4-dihydronaphthyl, etc. Preferred embodiments are 8 to 9 membered fused ring, which refer to cyclic structures containing 8 to 9 ring atoms within the above examples.

[0118] The term aryl used alone or in combination with other terms refers to a group selected from: [0119] a) 5- and 6-membered carbocyclic aromatic rings, e.g., phenyl; [0120] b) bicyclic ring systems such as 7 to 12 membered bicyclic ring systems, wherein at least one ring is carbocyclic and aromatic, e.g., naphthyl and indanyl; and, [0121] c) tricyclic ring systems such as 10 to 15 membered tricyclic ring systems wherein at least one ring is carbocyclic and aromatic, e.g., fluorenyl.

[0122] The terms aromatic hydrocarbon ring and aryl are used interchangeably throughout the disclosure herein. In some embodiments, a monocytic or bicyclic aromatic hydrocarbon ring has 5 to 10 ring-forming carbon atoms (i.e., C.sub.5-10 aryl). Examples of a monocyclic or bicyclic aromatic hydrocarbon ring includes, but not limited to, phenyl, naphth-1-yl, naphth-2-yl, anthracenyl, phenanthrenyl, and the like. In some embodiments, the aromatic hydrocarbon ring is a naphthalene ring (naphth-1-yl or naphth-2-yl) or phenyl ring. In some embodiments, the aromatic hydrocarbon ring is a, phenyl ring.

[0123] Specifically, the term bicyclic fused aryl refers to a bicyclic aryl ring as defined herein. The typical bicyclic fused aryl is naphthalene.

[0124] The term heteroaryl refers to a group selected from: [0125] a) 5-, 6- or 7-membered aromatic, monocyclic rings comprising at least one heteroatom, for example, from 1 to 4, or, in some embodiments, from 1 to 3, in some embodiments, from 1 to 2, heteroatoms, selected from nitrogen (N), sulfur (S) and oxygen (O), with the remaining ring atoms being carbon; [0126] b) 7- to 12-membered bicyclic rings comprising at least one heteroatom, for example, from 1 to 4, or, in some embodiments, from 1 to 3, or, in other embodiments, 1 or 2, heteroatoms, selected from N, O, and S, with the remaining ring atoms being carbon and wherein at least one ring is aromatic and at least one heteroatom is present in the aromatic ring; and [0127] c) 11- to 14-membered tricyclic rings comprising at least one heteroatom, for example, from 1 to 4, or in some embodiments, from 1 to 3, or, in other embodiments, 1 or 2, heteroatoms, selected from N, O, and S, with the remaining ring atoms being carbon and wherein at least one ring is aromatic and at least one heteroatom is present in an aromatic ring.

[0128] When the total number of S and O atoms in the heteroaryl group exceeds 1, those heteroatoms are not adjacent to one another. In some embodiments, the total number of S and O atoms in the heteroaryl group is not more than 2. In some embodiments, the total number of S and O atoms in the aromatic heterocycle is not more than 1. When the heteroaryl group contains more than one heteroatom ring member, the heteroatoms may be the same or different. The nitrogen atoms in the ring(s) of the heteroaryl group can be oxidized to form N-oxides.

[0129] Specifically, the term bicyclic fused heteroaryl refers to a 7- to 12-membered, preferably 7- to 10-membered, more preferably 9- or 10-membered fused bicyclic heteroaryl ring as defined herein. Typically, a bicyclic fused heteroaryl is 5-membered/5-membered, 5-membered/6-membered, 6-membered/6-membered, or 6-membered/7-membered bicyclic. The group can be attached to the remainder of the molecule through either ring.

[0130] Representative examples of bicyclic fused heteroaryl include, but not limited to, the following groups benzisoxazolyl, benzodiazolyl, benzofuranyl, benzofurazanyl, benzofuryl, 1c benzoimidazolyl, benzoisothiazolyl, benzothiadiazolyl, benzothiazolyl, benzothienyl, benzothiophenyl, benzotriazolyl, benzoxadiazolyl, benzoxazolyl, furopyridinyl, furopyrrolyl, imidazopyridinyl, imidazopyridyl, imidazothiazolyl, indazolyl, indolizinyl, indolyl, isobenzofuryl, isoindolyl, isoquinolinyl (or isoquinolyl), naphthyridinyl, phthalazinyl, pteridinyl, purinyl, pyrazinopyridazinyl, pyrazolopyridinyl, pyrazolopyrimidinyl, pyrazolopyridyl, pyrazolotriazinyl, pyrazolopyridyl, pyrrolopyridinyl, quinazolinyl, quinolinyl (or quinolyl), quinoxalinyl, thiazolopyridyl, thienopyrazinyl, thienopyrazolyl, thienopyridyl, thienopyrrolyl, thienothienyl, or triazolopyridyl.

[0131] The term a benzo fused heteroaryl is a bicyclic fused heteroaryl in which a 5- to 7-membered (preferably, 5- or 6-membered) monocyclic heteroaryl ring as defined herein fused to a benzene ring.

[0132] The terms aromatic heterocyclic ring and heteroaryl are used interchangeably throughout the disclosure herein. In some embodiments, a monocyclic or bicyclic aromatic heterocyclic ring has 5-, 6-, 7-, 8-, 9- or 10 O-ring forming members with 1, 2, 3, or 4 heteroatom ring members independently selected from nitrogen (N), sulfur (S) and oxygen (O) and the remaining ring members being carbon. In some embodiments, the monocyclic or bicyclic aromatic heterocyclic ring is a monocyclic or bicyclic ring comprising 1 or 2 heteroatom ring members independently selected from nitrogen (N), sulfur (S) and oxygen (O). In some embodiments, the monocyclic or bicyclic aromatic heterocyclic ring is a 5- to 6-membered heteroaryl ring, which is monocyclic and which has 1 or 2 heteroatom ring members independently selected from nitrogen (N), sulfur (S) and oxygen (O). In some embodiments, the monocyclic or bicyclic aromatic heterocyclic ring is an 8- to 10-membered heteroaryl ring, which is bicyclic and which has 1 or 2 heteroatom ring members independently selected from nitrogen, sulfur and oxygen.

[0133] Examples of the heteroaryl group or the monocyclic or bicyclic aromatic heterocyclic ring include, but are not limited to, (as numbered from the linkage position assigned priority 1) pyridyl (such as 2-pyridyl, 3-pyridyl, or 4-pyridyl), cinnolinyl, pyrazinyl, 2,4-pyrimidinyl, 3,5-pyrimidinyl, 2,4-imidazolyl, imidazopyridinyl, isoxazolyl, oxazolyl, thiazolyl, isothiazolyl, thiadiazolyl (such as 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, or 1,3,4-thiadiazolyl), tetrazolyl, thienyl (such as thien-2-yl, thien-3-yl), triazinyl, benzothienyl, furyl or furanyl, benzofuryl, benzoimidazolyl, indolyl, isoindolyl, oxadiazolyl (such as 1,2,3-oxadiazolyl, 1,2,4-oxadiazolyl, or 1,3,4-oxadiazolyl), phthalazinyl, pyrazinyl, pyridazinyl, pyrrolyl, triazolyl (such as 1,2,3-triazolyl, 1,2,4-triazolyl, or 1,3,4-triazolyl), quinolinyl, isoquinolinyl, pyrazolyl, pyrrolopyridinyl (such as 1H-pyrrolo[2,3-b]pyridin-5-yl), pyrazolopyridinyl (such as 1H-pyrazolo[3,4-b]pyridin-5-yl), benzoxazolyl (such as benzo[d]oxazol-6-yl), pteridinyl, purinyl, 1-oxa-2,3-diazolyl, 1-oxa-2,4-diazolyl, 1-oxa-2,5-diazolyl, 1-oxa-3,4-diazolyl, 1-thia-2,3-diazolyl, 1-thia-2,4-diazolyl, 1-thia-2,5-diazolyl, 1-thia-3,4-diazolyl, furazanyl (such as furazan-2-yl, furazan-3-yl), benzofurazanyl, benzothiophenyl, benzothiazolyl, benzoxazolyl, quinazolinyl, quinoxalinyl, naphthyridinyl, furopyridinyl, benzothiazolyl (such as benzo[d]thiazol-6-yl), and indazolyl (such as 1H-indazol-5-yl).

[0134] Heterocyclyl heterocycle or heterocyclic are interchangeable and refer to a non-aromatic heterocyclyl group comprising one or more heteroatoms selected from nitrogen, oxygen, silicon or optionally oxidized sulfur as ring members, with the remaining ring members being carbon, including monocyclic, fused ring, i.e., containing monocyclic heterocyclyl, and fused heterocyclic groups, bridged heterocyclic groups or spiro heterocyclic groups.

[0135] The term optionally oxidized sulfur used herein refers to S, SO or SO.sub.2.

[0136] The term monocyclic heterocyclyl refers to noncyclic groups in which at least one ring member (e.g., 1-3 heteroatoms, 1 or 2 heteroatom(s)) is a heteroatom selected from nitrogen, oxygen, silicon or optionally oxidized sulfur. A heterocycle may be saturated or partially saturated (i.e., not forming a completely conjugated pi-electron system).

[0137] Exemplary noncyclic 4 to 9-membered heterocyclyl groups include, but not limited to, pyrrolidin-1-yl, pyrrolidin-2-yl, pyrrolidin-3-yl, imidazolidin-2-yl, imidazolidin-4-yl, pyrazolidin-2-yl, pyrazolidin-3-yl, piperidin-1-yl, piperidin-2-yl, piper din-3-yl, piperidin-4-yl, 2,5-piperazinyl, pyranyl, morpholinyl, morpholino, morpholin-2-yl, morpholin-3-yl, oxiranyl, aziridin-1-yl, aziridin-2-yl, azocan-1-yl, azocan-2-yl, azocan-3-yl, azocan-4-yl, azocan-5-yl, thiiranyl, azetidin-1-yl, azetidin-2-yl, azetidin-3-yl, oxetanyl, thietanyl, 1,2-dithietanyl, 1,3-dithietanyl, dihydropyridinyl, tetrahydropyridinyl, thiomorpholinyl, thioxanyl, piperazinyl, homopiperazinyl, homopiperidinyl, azepan-1-yl, azepan-2-yl, azepan-3-yl, azepan-4-yl, oxepanyl, thiepanyl, 1,4-oxathianyl, 1,4-dioxepanyl, 1,4-oxathiepanyl, 1,4-oxazepanyl, 1,4-dithiepanyl, 1,4-thiazepanyl and 1,4-diazepanyl, 1,4-dithianyl, 1,4-azathianyl, oxazepinyl, diazepinyl, thiazepinyl, dihydrothienyl, dihydropyranyl, dihydrofuranyl, tetrahydrofuranyl, tetrahydrothienyl, tetrahydropyranyl, tetrahydrothiopyranyl, 1-pyrrolinyl, 2-pyrrolinyl, 3-pyrrolinyl, indolinyl, 2H-pyranyl, 4H-pyranyl, 1,4-dioxanyl, 1,3-dioxolanyl, pyrazolinyl, pyrazolidinyl, dithianyl, dithiolanyl, pyrazolidinyl, imidazolinyl, pyrimidinonyl, 1,1-dioxo-thiomorpholinyl, oxazolidinyl, or oxazolidin-4-yl.

[0138] The term fused heterocyclyl refers to a 5 to 20-membered polycyclic heterocyclyl group, wherein each ring in the system shares an adjacent pair of atoms (carbon and carbon atoms or carbon and nitrogen atoms) with another ring, comprising one or more heteroatoms selected from nitrogen, oxygen or optionally oxidized sulfur as ring members, with the remaining ring members being carbon. One or more rings of a fused heterocyclic group may contain one or more double bonds, but the fused heterocyclic group does not have a completely conjugated pi-electron system. Preferably, a fused heterocyclyl is 6 to 14-membered, and more preferably 7 to 12-membered, or 7- to 10-membered. According to the number of membered rings, a fused heterocyclyl is divided into bicyclic, tricyclic, tetracyclic, or polycyclic fused heterocyclyl. The group can be attached to the remainder of the molecule through either ring.

[0139] Specifically, the term bicyclic fused heterocyclyl refers to a 7 to 12-membered, preferably 7- to 10-membered, more preferably 9- or 10-membered fused heterocyclyl as defined herein comprising two fused rings and comprising 1 to 4 heteroatoms selected from nitrogen, oxygen or optionally oxidized sulfur as ring members. Typically, a bicyclic fused heterocyclyl is 5-membered/5-membered, 5-membered/6-membered, 6-membered/6-membered, or 6-membered/7-membered bicyclic fused heterocyclyl Representative examples of (bicyclic) fused heterocycles include, but not limited to, the following groups octahydrocyclopenta[c]pyrrole, octahydropyrrolo[3,4-c]pyrrolyl, octahydroisoindolyl, isoindolinyl, octahydro-benzo[b][1,4]dioxin, indolinyl, isoindolinyl, benzopyranyl, dihydrothiazolopyrimidinyl, tetrahydroquinolyl, tetrahydroisoquinolyl (or tetrahydroisoquinolinyl), dihydrobenzofuranyl, dihydrobenzoxazinyl, dihydrobenzoimidazolyl, tetrahydrobenzothienyl, tetrahydrobenzofuranyl, benzodioxolyl, benzodioxonyl, chronmanyl, chromenyl, octahydrochromenyl, dihydrobenzodioxvnyl, dihydrobenzoxezinyl, dihydrobenzodioxepinyl, dihydrothienodioxynyl, dihydrobenzooxazepinyl, tetrahydrobenzooxazepinyl, dihydrobenzoazepinyl, tetrahydrobenzoazepinyl, isochromanyl, chromanyl, or tetrahydropyrazolopyrimidinyl (e.g., 4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidin-3-yl).

[0140] The term a benzo fused heterocyclyl is a bicyclic fused heterocyclyl in which a monocyclic 4 to 9-membered heterocyclyl as defined herein (preferably 5- or 6-membered) fused to a benzene ring.

[0141] The term bridged heterocyclyl refers to a 5- to 14-membered polycyclic heterocyclic alkyl group, wherein every two rings in the system share two disconnected atoms, comprising one or more heteroatoms selected from nitrogen, oxygen or optionally oxidized sulfur as ring members, with the remaining ring members being carbon. Specifically, the bridge including the two bridgeheads contains 1-6 atoms selected from carbon, oxygen, nitrogen and sulfur with no two heteroatoms (oxygen nitrogen and sulfur) being connected to each other. One or more rings of a bridged heterocyclyl group may contain one or more double bonds, but none of the rings has a completely conjugated pi-electron system. Preferably, a bridged heterocyclyl is 6- to 14-membered, or 7- to 12-membered, and more preferably 7 to 10-membered. According to the number of membered rings, a bridged heterocyclyl is divided into bicyclic, tricyclic, tetracyclic or polycyclic bridged heterocyclyl, and preferably refers to bicyclic, tricyclic or tetracyclic bridged heterocyclyl, and more preferably bicyclic or tricyclic bridged heterocyclyl. Representative examples of bridged heterocyclyls include, but not limited to, the following groups: 2-azabicyclo[2.2.1]heptyl, azabicyclo[3.1.0]hexyl, 2-azabicyclo[2.2.2]octyl and 2-azabicyclo[3,3,2]decyl.

[0142] Spiro heterocyclyl refers to a 5- to 20-membered polycyclic heterocyclyl with rings connected through one common carbon atom (called a spiro atom), wherein said rings have one or more heteroatoms selected from the group consisting of N, O, S, SO or SO.sub.2 heteroatoms as ring atoms, with the remaining ring atoms being C. Preferably a spiro heterocyclyl is 6- to 14-membered, and more preferably 7- to 10-membered. According to the number of common spiro atoms, a spiro heterocyclyl is divided into mono-spiro heterocyclyl, di-spiro heterocyclyl, or poly-spiro heterocyclyl, and preferably refers to mono-spiro heterocyclyl or di-spiro heterocyclyl, and more preferably 4-membered/4-membered, 4-membered/5-membered, 4-membered/6-membered, 5-membered/5-membered, or 5-membered/6-membered mono-spiro heterocyclyl. Representative examples of spiro heterocyclyls include, but are not limited to the following groups: 1,7-dioxaspiro[4,5]decyl, 2-oxa-7-aza-spiro[4.4]nonyl, 7-oxa spiro[3,5]nonyl, 5-oxa-spiro[2.4]heptyl, and 2-oxa-6-azaspiro[3.3]heptyl.

[0143] N-linked heterocyclyl disclosed herein refers to a heterocyclyl group which is connected to the other part of the molecule by a bond from a nitrogen atom of the heterocyclyl ring. N-linked heterocyclyl comprising 0, 1 or 2 additional heteroatoms selected from nitrogen, oxygen or optionally oxidized sulfur as ring member(s) refers to a heterocyclyl group which is connected to the other part of the molecule by a bond from a, nitrogen atom of the heterocyclyl ring, and which comprises 0, 1 or 2 additional heteroatoms in addition to the nitrogen atom linked to the other part of the molecule.

[0144] C-linked heterocyclyl disclosed herein refers to a heterocyclyl group which is connected to the other part of the molecule by a bond from a carbon atom of the heterocyclyl ring. Si-linked heterocyclyl disclosed herein refers to a heterocyclyl group which is connected to the other part of the molecule by a bond from a silicon atom of the heterocyclyl ring.

[0145] The term at least one substituent disclosed herein includes, for example, from 1 to 4, such as from 1 to 3, further as 1 or 2, substituents, provided that the theory of valence is met. For example, at least one substituent R.sup.d disclosed herein includes from 1 to 4, such as from 1 to 3, further as 1 or 2, substituents selected from the list of R.sup.d as disclosed herein.

[0146] Compounds disclosed herein may contain an asymmetric center and may thus exist as enantiomers. Enantiomers refer to two stereoisomers of a compound which are non-superimposable mirror images of one another. Where the compounds disclosed herein possess two or more asymmetric centers, they may additionally exist as diastereomers. Enantiomers and diastereomers fall within the broader class of stereoisomers. All such possible stereoisomers as substantially pure resolved enantiomers, racemic mixtures thereof, as well as mixtures of diastereomers are intended to be included. All stereoisomers of the compounds disclosed herein and/or pharmaceutically acceptable salts thereof are intended to be included. Unless specifically mentioned otherwise, the reference to one isomer applies to any of the possible isomers. Whenever the isomeric composition is unspecified, all possible isomers are included.

[0147] Compounds disclosed herein also comprise deuterated compounds. The term deuterated compound refers to a compound wherein one or more carbon-bound hydrogen(s) are replaced by one or more deuterium(s). Similarly, the term deuterated is be used herein to modify a chemical structure or an organic group or radical, wherein one or more carbon-bound hydrogen(s) are replaced by one or more deuterium(s), e.g., deuterated-alkyl, deuterated-cycloakyl, deuterated-heterocycloalkyl deuterated-aryl, deuterated-morpholinyl, and the like. For example, the term deuterated-alkyl defined above refers to an alkyl group as defined herein, wherein at least one hydrogen atom bound to carbon is replaced by a deuterium. In a deuterated alkyl group, at least one carbon atom is bound to a deuterium; and it is possible for a carbon atom to be bound to more than one deuterium; it is also possible that more than one carbon atom in the alkyl group is bound to a deuterium.

[0148] The term substantially pure as used herein means that the target stereoisomer contains no more than 35%, such as no more than 30%, further such as no more than 25%, even further such as no more than 20%, by weight of any other stereoisomer(s). In some embodiments, the term substantially pure means that the target stereoisomer contains no more than 10%, for example, no more than 5%, such as no more than 1%, by weight of any other stereoisomer(s).

[0149] When compounds disclosed herein contain olefinic double bonds, unless specified otherwise, such double bonds are meant to include both E and Z geometric isomers.

[0150] When compounds disclosed herein contain a di-substituted cyclic ring system, substituents found on such ring system may adopt cis and trans formations. Cis formation means that both substituents are found on the upper side of the 2 substituent placements on the carbon, while trans would mean that they were on opposing sides. For example, the di-substituted cyclic ring system may be cyclohexyl or cyclobutyl ring.

[0151] It may be advantageous to separate reaction products from one another and/or from starting materials. The desired products of each step or series of steps is separated and/or purified (hereinafter separated) to the desired degree of homogeneity by the techniques common in the art. Typically such separations involve multiphase extraction, crystallization from a, solvent or solvent mixture, distillation, sublimation, or chromatography. Chromatography can involve any number of methods including, for example: reverse-phase and normal phase; size exclusion; ion exchange; high, medium and low pressure liquid chromatography methods and apparatus; small scale analytical; simulated moving bed (SMB) and preparative thin or thick layer chromatography, as well as techniques of small scale thin layer and flash chromatography. One skilled in the art will apply techniques most likely to achieve the desired separation.

[0152] Diastereomers refers to stereoisomers of a compound with two or more chiral centers but which are not mirror images of one another. Diastereomeric mixtures can be separated into their individual diastereomers on the basis of their physical chemical differences by methods well known to those skilled in the art, such as by chromatography and/or fractional crystallization. Enantiomers can be separated by converting the enantiomeric mixture into a diastereomeric mixture by reaction with an appropriate optically active compound (e.g., chiral auxiliary such as a chiral alcohol or Mosher's acid chloride), separating the diastereomers and converting (e.g., hydrolyzing) the individual diastereoisomers to the corresponding pure enantiomers. Enantiomers can also be separated by use of a chiral HPLC column.

[0153] A single stereoisomer, e.g., a substantially pure enantiomer, may be obtained by resolution of the racemic mixture using a method such as formation of diastereomers using optically active resolving agents (Eliel, K. and Wilen, S. Stereochemistry of Organic Compounds. New York: John Wiley & Sons, Inc., 1994: Lochnmuller, C. H., et al. Chromatographic resolution of enantiomers: Selective review. J. Chromatogr., 113(3) (1975): pp. 283-302). Racemic mixtures of chiral compounds of the invention can be separated and isolated by any suitable method, including: (1) formation of ionic, diastereomeric salts with chiral compounds and separation by fractional crystallization or other methods, (2) formation of diastereomeric compounds with chiral derivatizing reagents, separation of the diastereomers, and conversion to the pure stereoisomers, and (3) separation of the substantially pure or enriched stereoisomers directly under chiral conditions. See: Wainer, Irving W, Ed. Drug Stereochemistry: Analytical Methods and Pharmacology New York: Marcel Dekker, Inc., 1993.

[0154] The configuration of diastereomeric or enantiomeric isomers could be assigned by technologies including but not limited to: 1D- or 2D-NMR spectroscopy of compounds or their derivatives (e.g. Mosher ester); optical rotatory dispersion; circular dichroism spectroscopy; X-ray diffractometry; in silico calculation (e.g. QM or MMGBSA).

[0155] Pharmaceutically acceptable salts refers to those salts which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of humans and lower animals without undue toxicity, irritation, allergic response and the like, and are commensurate with a reasonable benefit/risk ratio. A pharmaceutically acceptable salt may be prepared in situ during the final isolation and purification of the compounds disclosed herein, or separately by reacting the free base function with a suitable organic acid or by reacting the acidic group with a suitable base.

[0156] In addition, if a compound disclosed herein is obtained as an acid addition salt, the free base can be obtained by basifying a solution of the acid salt. Conversely, if the product is a free base, an addition salt, such as a pharmaceutically acceptable addition salt, may be produced by dissolving the free base in a suitable organic solvent and treating the solution with an acid, in accordance with conventional procedures for preparing acid addition salts from base compounds.

[0157] Those skilled in the art will recognize various synthetic methodologies that may be used without undue experimentation to prepare non-toxic pharmaceutically acceptable addition salts.

[0158] As defined herein, a pharmaceutically acceptable salt thereof include salts of at least one compound of Formula (I), and salts of the stereoisomers of the compound of Formula (I), such as salts of enantiomers, and/or salts of diastereomers.

[0159] The terms administration, administering. treating and treatment herein, when applied to an animal, human, experimental subject, cell, tissue, organ, or biological fluid, mean contact of an exogenous pharmaceutical, therapeutic, diagnostic agent, or composition to the animal, human, subject, cell, tissue, organ, or biological fluid. Treatment of a cell encompasses contact of a reagent to the cell, as well as contact of a reagent to a fluid, where the fluid is in contact with the cell. The term administration and treatment also means in vitro and ex vivo treatments, e.g., of a cell, by a reagent, diagnostic, binding compound, or by another cell. The term subject herein includes any organism, preferably an animal, more preferably a mammal (e.g., rat, mouse, dog, cat, and rabbit) and most preferably a human.

[0160] The term effective amount or therapeutically effective amount refers to an amount of the active ingredient, such as compound that, when administered to a subject for treating a disease, or at least one of the clinical symptoms of a disease or disorder, is sufficient to affect such treatment for the disease, disorder, or symptom. The therapeutically effective amount can vary with the compound, the disease, disorder, and/or symptoms of the disease or disorder, severity of the disease, disorder, and/or symptoms of the disease or disorder, the age of the subject to be treated, and/or the weight of the subject to be treated. An appropriate amount in any given instance can be apparent to those skilled in the art or can be determined by routine experiments. In some embodiments, therapeutically effective amount is an amount of at least one compound and/or at least one stereoisomer thereof, and/or at least one pharmaceutically acceptable salt thereof disclosed herein effective to treat as defined herein, a disease or disorder in a subject. In the case of combination therapy, the therapeutically effective amount refers to the total amount of the combination objects for the effective treatment of a disease, a disorder or a condition.

[0161] The pharmaceutical composition comprising the compound disclosed herein can be administrated via oral, inhalation, rectal, parenteral or topical administration to a subject in need thereof. For oral administration, the pharmaceutical composition may be a regular solid formulation such as tablets, powder, granule, capsules and the like, a liquid formulation such as water or oil suspension or other liquid formulation such as syrup, solution, suspension or the like; for parenteral administration, the pharmaceutical composition may be solution, water solution, oil suspension concentrate, lyophilized powder or the like. Preferably, the formulation of the pharmaceutical composition is selected from tablet, coated tablet, capsule, suppository, nasal spray or injection, more preferably tablet or capsule. The pharmaceutical composition can be a single unit administration with an accurate dosage. In addition, the pharmaceutical composition may further comprise additional active ingredients.

[0162] All formulations of the pharmaceutical composition disclosed herein can be produced by the conventional methods in the pharmaceutical field. For example, the active ingredient can be mixed with one or more excipients, then to make the desired formulation. The pharmaceutically acceptable excipient refers to conventional pharmaceutical carriers suitable for the desired pharmaceutical formulation, for example: a diluent, a vehicle such as water, various organic solvents, etc., a filler such as starch, sucrose, etc. a binder such as cellulose derivatives, alginates, gelatin and polyvinylpyrrolidone (PVP); a wetting agent such as glycerol; a disintegrating agent such as agar, calcium carbonate and sodium bicarbonate; an absorption enhancer such as quatemary ammonium compound; a surfactant such as hexadecanol; an absorption carrier such as Kaolin and soap clay; a lubricant such as talc, calcium stearate, magnesium stearate, polyethylene glycol, etc. In addition, the pharmaceutical composition further comprises other pharmaceutically acceptable excipients such as a decentralized agent, a stabilizer, a thickener, a complexing agent, a buffering agent, a permeation enhancer, a polymer, aromatics, a sweetener, and a dye.

[0163] The term disease refers to any disease, discomfort, illness, symptoms or indications, and can be interchangeable with the term disorder or condition.

[0164] Throughout this specification and the claims which follow, unless the context requires otherwise, the term comprise, and variations such as comprises and comprising are intended to specify the presence of the features thereafter, but do not exclude the presence or addition of one or more other features. When used herein the term comprising can be substituted with the term containing. including or sometimes having.

[0165] Throughout this specification and the claims which follow, the term C.sub.n_. indicates a range which includes the endpoints, wherein n and m are integers and indicate the number of carbons. Examples include C.sub.1-8, C.sub.1-6, and the like.

[0166] Unless specifically defined elsewhere in this document, all other technical and scientific terms used herein have the meaning commonly understood by one of ordinary skill in the art to which this invention belongs.

General Synthesis

[0167] Compounds disclosed herein, including salts thereof, can be prepared using known organic synthesis techniques and can be synthesized according to any of numerous possible synthetic routes.

[0168] The reaction for preparing compounds disclosed herein can be carried out in suitable solvents which can be readily selected by one of skill in the art of organic synthesis. Suitable solvents can be substantially non-reactive with the starting materials, the intermediates, or products at the temperatures at which the reactions are carried out, e.g., temperatures which can range from the solvent's boiling temperature. A given reaction can be carried out in one solvent or mixture of solvents.

[0169] The selection of appropriate protecting group, can be readily determined by one skilled in the art.

[0170] Reactions can be monitored according to any suitable method known in the art, such as NMR, UV, HPLC, LC-MS and TLC. Compounds can be purified by a variety of methods, including HPLC and normal phase silica chromatography.

[0171] Chiral analytic HPLC was used for the retention time analysis of different chiral examples, the conditions were divided into the methods as below according to the column, mobile phase, solvent ratio used.

##STR00092##

[0172] For example, compounds of Formula (I) can be formed as shown in Scheme I. Compound (i) can be deprotonated and react with 2-amino-3,5-dihalopyrazine (i) to give compound (iii), compound (iii) can be coupled with compound (iv) using transition metal catalyzed reaction to give compound (v) [i.e., Formula (I)].

##STR00093##

[0173] For example, compounds of Formula (I) can be formed as shown in Scheme II. Compound (i) can be coupled with 2-amino-3,5-dihalopyrazine (ii) to give compound (iii), which is then reacted with a deprotonated compound (iv) to give compound (v) [i.e., Formula (I)].

##STR00094##

[0174] For example, compounds of Formula (I) can be formed as shown in Scheme III. Compound (i) can be deprotonated and react with 2-amino-3,5-dihalopyrazine (ii) to give compound (iii); compound (iii) can be borylated to give compound (iv); compound (iv) can be coupled with compound (v) using transition metal catalyzed reaction to give compound (vi) [i.e., Formula (I)].

ABBREVIATIONS

[0175] Et ethyl [0176] Ac acetyl [0177] THF tetrahydrofuran [0178] Boc tert-butyloxycarbonyl [0179] LC-MS liquid chromatograph mass spectrometer [0180] DMF N,N-dimethylformamide [0181] PE petroleum ether [0182] DCM dichloromethane [0183] BPD bis(pinacolato)diboron [0184] dppf 1,1-bis(diphenylphosphino)ferrocene [0185] Me methyl [0186] DMSO dimethyl sulfoxide [0187] DIPEA N,N-diisopropylethylamine [0188] HATU 2-(7-azabenzotriazol-1-yl)N,N,N,N-tetramethyluronium hexafluorophosphate [0189] NMR nuclear magnetic resonance [0190] HPLC high performance liquid chromatography [0191] Pr propyl [0192] Ms methanesulfonyl [0193] DIAD diisopropyl azodicarboxylate [0194] Ph phenyl [0195] DMAC dimethylacetamide [0196] TMS trimethylsilyl [0197] Bu butyl [0198] NCS N-chlorosuccinimide [0199] XPhos dicyclohexyl(2,4,6-triisopropyl-[1,1-biphenyl]-2-yl)phosphane [0200] dba dibenzylideneacetone [0201] JohnPhos (2-biphenyl)di-tert-butylphosphine [0202] TEMPO 2,2,6,6-tetramethylpiperidinooxy [0203] TLC thin layer chromatography [0204] TFA trifluoroacetic acid [0205] XantPhos 4,5-Bis(diphenylphosphino)-9,9-dimethylxanthene [0206] tR retention time [0207] TBS tert-butyldimethylsilyl [0208] TBAF tetra-n-butylammonium fluoride [0209] DCE dichloroethane [0210] NBS N-bromosuccinimide [0211] Ts p-toluenesulfonyl [0212] MTBE methyl tert-butyl ether

Example A1

4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-N-(2-(dimethylamino)ethyl)-2,6-dimethylbenzamide

[0213] ##STR00095##

Step 1: tert-butyl 4-(4-hydroxy-1H-pyrazol-1-yl)piperidine-1-carboxylate

[0214] ##STR00096##

[0215] To a mixture of tert-butyl 4-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)piperidine-1-carboxylate (23.5 g, 62.3 mmol) and NaOH (4.98 g, 124.5 mmol) in THF (400 mL) and water (80 mL) was added 30% H.sub.2O.sub.2 (14.2 g, 124.5 mmol) dropwise at 0? C., then the mixture was warmed to room temperature and stirred for 1 h. Saturated Na.sub.2S.sub.2O.sub.3 (50 mL) was added and the mixture was extracted with EtOAc (300 mL?2). The combined organic layer was washed with brine (100 mL), dried over Na.sub.2SO.sub.4, filtered, and the filtrate was concentrated under reduced pressure to give the title compound (14.5 g, 87%). LCMS (M+H).sup.+=268.

Step 2: tert-butyl 4-(4-((3-amino-6-bromopyrazin-2-yl)oxy)-1H-pyrazol-1-yl)piperidine-1-carboxylate

[0216] ##STR00097##

[0217] A mixture of tert-butyl 4-(4-hydroxy-1H-pyrazol-1-yl)piperidine-1-carboxylate (14.5 g, 54.2 mmol), Cs.sub.2CO.sub.3 (35.2 g. 108.4 mmol) and 3,5-dibromopyrazin-2-amine (13.7 g, 54.2 mmol) in DMF (250 mL) was stirred at 90? C. for 2 h then cooled to room temperature. Water (6(0) mL) was added and the mixture was extracted with EtOAc (500 mL?2). The combined organic layer was successively washed with water (300 mL?3), brine (300 mL), dried over Na.sub.2SO.sub.4, filtered, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel chromatography (PE/EtOAc=5/1 to 1/1) to give the title compound (18.5 g, 78%). LCMS (M+H)+=439, 441.

Step 3: 5-bromo-3-((1-(piperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine hydrochloride

[0218] ##STR00098##

[0219] To a solution of tert-butyl 4-(4-((3-amino-6-bromopyrazin-2-yl)oxy)-1H-pyrazol-1-yl)piperidine-1-carboxylate (18.5 g, 42.1 mmol) in dioxane (100 mL) was added HCl in dioxane (42.1 mL, 4 M, 168.4 mmol). The mixture was stirred for 2 h at room temperature. The precipitate was collected by filtration to give the title compound (15.8 g, 100%). LCMS (M+H).sup.+=339, 341.

Step 4: 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine

[0220] ##STR00099##

[0221] To a solution of 5-bromo-3-((1-(piperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine hydrochloride (13 g, 34.6 mmol) in MeOH (200 mL) was added 37% HCHO solution (11 mL, 138.5 mmol) and NaBH(OAc).sub.3 (14.6 g, 69.2 mmol) at room temperature and the mixture was stirred for 16 h. The mixture was concentrated in vacuo, diluted with saturated NaHCO.sub.3 solution (200 mL) and extracted with DCM (400 mL?2). The combined organic layer was washed with brine (100 mL), dried over anhydrous Na.sub.2SO.sub.4, filtered and the filtrated was concentrated under reduced pressure to give the title compound (12.0 g, 89%). LCMS (M+H).sup.+=353, 355.

Step 5: 4-bromo-N-(2-(dimethylamino)ethyl-2,6-dimethylbenzamide

[0222] ##STR00100##

[0223] A solution of 4-bromo-2,6-dimethylbenzoic acid (4.2 g, 18.3 mmol) in SOCl.sub.2 (30 mL) was stirred at reflux for 1 h then cooled to room temperature. The solvent was concentrated under reduced pressure. The residue was dissolved in dry DCM (50 mL) then N1,N1-dimethylethane-1,2-diamine (2.42 g, 27.5 mmol) and triethylamine (2.8 g, 27.5 mmol) was added dropwise at 0? C. The mixture was stirred for 3 h at room temperature, then quenched with saturated NaHCO.sub.3 solution (50 mL) and extracted with DCM (50 mL?2). The combined organic layer was washed with brine (50 mL), dried over anhydrous Na.sub.2SO.sub.4, filtered and the filtrate was concentrated under reduced pressure to give the title compound (5.4 g, 98%). LCMS (M+H).sup.+=299, 301.

Step 6: N-(2-(dimethylamino)ethyl)-2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide

[0224] ##STR00101##

[0225] A mixture of 4-bromo-N-(2-(dimethylamino)ethyl)-2,6-dimethylbenzamide (5.4 g, 18 mmol), BPD (6.0 g, 23 mmol). Pd(dppf)Cl.sub.2 (659 mg, 0.9 mmol) and AcOK (3.53 g, 36 mmol) in dioxane (70 mL) was heated to reflux under nitrogen overnight. The solution was cooled to room temperature, diluted with EtOAc (50 mL) and washed with brine (30 mL). The aqueous layer was extracted with EtOAc (100 mL). The combined organic layer was dried over Na.sub.2SO.sub.4, filtered and the filtrate was concentrated under reduced pressure. The crude was purified by silica gel chromatography (DCM/MeOH=30/1 to 20/1) to give the title compound (4.5 g, 72%). LC-MS (M+H).sup.+=347.1.

Step 7: 4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-N-(2-(dimethylamino)ethyl)-2,6-dimethylbenzamide

[0226] To a solution of 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine (1.6 g, 4.5 mmol) and N-(2-(dimethylamino)ethyl)-2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide (1.87 g, 5.4 mmol) in dioxane (50 mL) and water (10 mL) was added K.sub.2CO.sub.3 (1.24 g, 9.0 mmol) and Pd(dppf)Cl.sub.2 (0.2 g, 0.27 mmol) under nitrogen atmosphere. The mixture was stirred for 15 h at 90? C., then cooled to room temperature. The mixture was extracted with EtOAc (50 mL?3). The combined organic layer was concentrated under reduced pressure. The residue was purified by silica gel chromatography (DCM/MeOH=40/1 to 20/1) to give Example A1 (1.05 g, 47%). .sup.1H NMR (400 MHz, DMSO-d6) ? 8.23 (s, 1H), 8.2-8.14 (m, 1H), 8.11 (s, 1H), 7.58 (s, 1H), 7.49 (s, 2H), 6.72 (s, 2H), 4.18-4.06 (m, 1H), 3.25-3.32 (m, 2H), 2.90-2.80 (m, 2H), 2.42-2.34 (m, 2H), 2.23 (s, 6H), 2.20 (s, 3H), 2.18 (s, 6H), 2.12-1.93 (m, 6H). LCMS (M+H).sup.+=493.5.

Example A2

3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-N,5-dimethylbenzenesulfonamide

[0227] ##STR00102##

Step 1: 3-bromo-5-methylbenzenesulfonyl chloride

[0228] ##STR00103##

[0229] SOCl.sub.2 (35.2 g, 295.6 mmol) was added to water (200 mL) dropwise at 0? C. and stirred at room temperature for overnight. The solution was cooled to 0? C. then CuCl (5.32 g, 53.8 mmol) was added, then the mixture was stirred at room temperature for 30 min to give mixture A. In a separated vessel, 3-bromo-5-methylaniline (10.0 g, 53.8 mmol) was dissolved in concentrated HCl (150 mL) then a solution of NaNO.sub.2 (5.2 g, 75.3 mmol) in water (10 mL) was added dropwise at 0? C. and the mixture was stirred at room temperature for 30 min to give mixture B. Mixture B was added dropwise to mixture A at 0? C. and the final mixture was stirred at room temperature for 3 h. The reaction mixture was extracted with DCM (100 mL?3). The combined organic layer was washed with brine (100 mL), dried over Na.sub.2SO.sub.4 then filtered. The filtrate was concentrated under reduced pressure to give the title compound (11.9 g, 82%).

Step 2: 3-bromo-N,5-dimethylbenzenesulfonamide

[0230] ##STR00104##

[0231] To a solution of 3-bromo-5-methylbenzenesulfonyl chloride (500 mg, 1.86 mmol) in pyridine (5 mL) was added MeNH.sub.2 in THF (2.09 mL, 2 M, 4.18 mmol) at room temperature. The mixture was stirred for 2 h at room temperature then quenched with water (10 mL). The mixture was extracted with EtOAc (20 mL?3). The combined organic layer was washed with brine (10 mL), dried over Na.sub.2SO.sub.4 and filtered. The filtrate was concentrated under reduced pressure to give the title compound (238 mg, 49%). LC-MS (M+H).sup.+=266.0.

Step 3: N,3-dimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide

[0232] ##STR00105##

[0233] The title compound (101 mg, 42%) was prepared in a manner similar to that in Example A1 step 6 from 3-bromo-N,5-dimethylbenzenesulfonamide and BPD. LC-MS (M+H).sup.+=312.1.

Step 4: 3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-N,5-dimethylbenzenesulfonamide

[0234] Example A2 (16 mg, 4%) was prepared in a manner similar to that in Example A1 step 7 from N,3-dimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide and 5-bromo-3-(1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yloxy)pyrazin-2-amine. .sup.1H NMR (400 MHz DMSO-d6) ? 8.32 (s, 1H), 8.12 (s, 1H), 8.02 (s, 1H), 7.93 (s, 1H), 7.59 (s, 1H), 7.49 (s, 1H), 7.45-7.37 (m, 1H), 6.89 (s, 2H), 4.17-4.05 (m, 1H), 2.90-2.82 (m, 2H), 2.45-2.40 (m, 6H), 2.21 (s, 3H), 2.10-1.90 (m, 6H). LC-MS (M+H).sup.+=458.2.

Example A3

4-(5-amino-6-(1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yloxy)pyrazin-2-yl)-N,2,6-trimethylbenzamide

[0235] ##STR00106##

Step 1: 4-bromo-N,2,6-trimethylbenzamide

[0236] ##STR00107##

[0237] A solution of 4-bromo-2,6-dimethylbenzoic acid (5.0 g, 20.7 mmol), DIPEA (11.4 mL, 88.3 mmol), HATU (9.13 g, 22.8 mmol) and methylamine hydrochloride (2.95 g, 41.5 mmol) in DMF (20 mL) was stirred for 1 h at room temperature then concentrated under vacuum. The residue was purified by silica gel chromatography (PE/EtOAc=2/3) to give the title compound (4.5 g, 85%). LC-MS (M+1)+=242.1.

Step 2: N,2,6-trimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide

[0238] ##STR00108##

[0239] The title compound (206 mg, 45%) was prepared in a manner similar to that in Example A1 step 6 from 4-bromo-N,2,6-trimethylbenzamide and BPD. LC-MS (M+H).sup.+=290.2.

Step 3: 4-(5-amino-6-(1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yloxy)pyrazin-2-yl)-N,2,6-trimethylbenzamide

[0240] Example A3 (18 mg, 32%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-(1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yloxy)pyrazin-2-amine and N,2,6-trimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide. .sup.1H NMR (400 MHz, DMSO-d6) ? 8.22 (s, 1H), 8.15-8.07 (m, 2H), 7.57 (s, 1H), 7.48 (s, 2H), 6.70 (s, 1H), 4.19-4.03 (m, 1H), 2.88-2.79 (m, 2H), 2.74 (d, J=4.5 Hz, 3H), 2.23-2.16 (m, 9H), 2.12-1.86 (m, 6H). LC-MS (M+H).sup.+=436.3.

Example A4

4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethyl-N-(2-(pyrrolidin-1-yl)ethyl)benzamide

[0241] ##STR00109##

Step 1: 4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylbenzoic acid

[0242] ##STR00110##

[0243] To a solution of 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine (5.3 g, 15 mmol) and 2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoic acid (5.0 g, 18 mmol) in dioxane (100 mL) and water (30 mL) was added K.sub.2CO.sub.3 (4.14 g, 30 mmol) and Pd(dppf)Cl.sub.2 (0.73 g, 0.9 mmol) under nitrogen. After being stirred for 15 h at 90? C., the reaction mixture was cooled to room temperature and washed with EtOAc (50 mL). The aqueous phase was acidified to pH=2-3 with HCl (4 M). The precipitate was collected by filtration to give the title compound (3.2 g, 50.7%). LCMS (M+H)+=423.1.

Step 2: 4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethyl-N-(2-(pyrrolidin-1-yl)ethyl)benzamide

[0244] To a solution of 4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylbenzoic acid (60 mg, 0.14 mmol) in DMF (2.0 mL) was added DIPEA (57 mg, 0.42 mmol) and HATU (84 mg, 0.21 mmol) and 1-(2-aminoethyl)pyrrolidine (20 mg, 0.17 mmol) at room temperature. After 2 h, the mixture was extracted with DCM (4 mL?2). The combined organic layer was washed with brine (8 mL) and dried over anhydrous Na.sub.2SO.sub.4. After filtration, the filtrate was concentrated under reduced pressure. The crude product was purified by Prep-HPLC to give Example A4 (17 mg, 23%). .sup.1H NMR (400 MHz, CD.sub.3OD) ? 8.12 (s, 1H), 8.07 (s, 1H), 7.70 (s, 1H), 7.56-7.51 (m, 2H), 4.28-4.18 (m, 1H), 3.60-3.52 (m, 2H), 3.09-3.00 (m, 2H), 2.79-2.72 (m, 2H), 2.70-2.62 (m, 4H), 2.41-2.35 (m, 9H), 2.34-2.08 (m, 4H), 1.91-1.82 (m, 4H). LC-MS (M+H).sup.+=519.4.

Example A5

4-(5-amino-6-(1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yloxy)pyrazin-2-yl)-2,6-dimethyl-N-(2-(piperidin-1-yl)ethyl)benzamide

[0245] ##STR00111##

[0246] Example A5 (23 mg, 41%) was prepared in a manner similar to that in Example A4 step 2 from 4-(5-amino-6-(1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yloxy)pyrazin-2-yl)-2,6-dimethylbenzoic acid and 2-(piperidin-1-yl)ethanamine. .sup.1H NMR (400 MHz, DMSO-d6) ? 8.23 (s, 1H), 8.15-8.06 (m, 2H), 7.58 (s, 1H), 7.50 (s, 2H), 6.72 (s, 2H), 4.19-4.07 (m, 1H), 3.37-3.33 (m, 2H), 2.89-2.80 (m, 2H), 2.44-2.33 (m, 6H), 2.25 (s, 6H), 2.20 (s, 3H), 2.12-1.92 (m, 6H), 1.54-1.44 (m, 4H), 1.43-1.34 (m, 2H). LC-MS (M+H).sup.+=533.4.

Example A6

3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylbenzenesulfonamide

[0247] ##STR00112##

Step 1: 3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide

[0248] ##STR00113##

[0249] The title compound (90 mg, 69%) was prepared in a manner similar to that in Example A1 step 6 from 3-bromo-5-methylbenzenesulfonamide and BPD.

Step 2: 3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylbenzenesulfonamide

[0250] Example A6 (29 mg, 24%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and 3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide. .sup.1H NMR (400 MHz, DMSO-d6) ? 8.30 (s, 1H), 8.13 (s, 1H), 8.10 (s, 1H), 7.88 (s, 1H), 7.59 (s, 1H), 7.55 (s, 1H), 7.32 (s, 2H), 6.89 (s, 2H), 4.19-4.07 (m, 1H), 2.89-2.82 (m, 2H), 2.41 (s, 3H), 2.20 (s, 3H), 2.10-1.90 (m, 6H). LC-MS (M+H).sup.+=444.2.

Example A7

3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methoxy-N-methylbenzenesulfonamide

[0251] ##STR00114##

Step 1: 3-bromo-5-methoxy-N-methylbenzenesulfonamide

[0252] ##STR00115##

[0253] A solution of 3-bromo-5-methoxybenzenesulfonyl chloride (7.1 g, 25 mmol), methylamine hydrochloride (3.35 g, 50 mmol) and triethylamine (7.57 g, 75 mmol) in DCM (50 mL) was stirred at room temperature overnight. The mixture was concentrated under reduced pressure and the crude was purified by silica gel chromatography (PE/EtOAc=20/1 to 5/1) to give the title compound (3.0 g, 40%). LCMS (M+H).sup.+=280.1.

Step 2: 3-methoxy-N-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide

[0254] ##STR00116##

[0255] A mixture of 3-bromo-5-methoxy-N-methylbenzenesulfonamide (0.53 g, 1.9 mmol), BPD (0.53 g, 2.1 mmol), Pd(dppf)Cl.sub.2.Math.DCM (77.7 mg, 0.095 mmol) and AcOK (0.56 g, 5.7 mmol) in dioxane (15 mL) was warmed to reflux and stirred for overnight. After being cooled to room temperature, the mixture was filtered and the filtrate was concentrated under reduced pressure to give the title compound (0.60 g, 94%). LC-MS (M+H).sup.+=328.2.

Step 3: 3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methoxy-N-methylbenzenesulfonamide

[0256] Example A7 (16 mg, 20%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and 3-jo methoxy-N-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide. .sup.1H NMR (400 MHz, DMSO-d6) ? 8.35 (s, 1H), 8.09 (s, 1H), 7.81 (s, 1H), 7.69 (s, 1H), 7.67 (s, 1H), 7.47-7.39 (m, 1H), 7.18 (s, 1H), 6.91 (s, 2H), 4.17-4.03 (m, 1H), 3.87 (s, 3H), 2.89-2.82 (m, 2H), 2.46-2.41 (d, J=4.2 Hz, 3H), 2.21 (s, 3H), 2.09-1.94 (m, 6H). LCMS (M+H).sup.+=474.4.

Example A8

5-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-N,2,3-trimethylbenzemesulfonamide

[0257] ##STR00117##

Step 1: 5-bromo-2,3-dimethylaniline

[0258] ##STR00118##

[0259] To a solution of 5-bromo-1,2-dimethyl-3-nitrobenzene (2.0 g, 8.26 mmol) and NH.sub.4Cl (2.33 g, 41.3 mmol) in EtOH (12 mL) and H.sub.2O (24 mL) was added iron powder (2.43 g, 41.3 mmol). The mixture was stirred for 2 h at 80? C. under nitrogen atmosphere. The mixture was cooled to room temperature and filtered. The filter cake was rinsed with DCM (10 mL?3) then the filtrate was concentrated under reduced pressure. The residue was diluted with water (10 mL) then was extracted with DCM (10 mL?2). The combined organic layer was washed with brine (10 mL), dried over anhydrous Na.sub.2SO.sub.4 then filtered. The filtrate was concentrated under reduced pressure and the residue was purified by silica gel chromatography (EtOAc/PE 0:1 to 1:9) to give the title compound (1.4 g, 85%). LC-MS (M+H).sup.+=199.8.

Step 2: 5-bromo-2,3-dimethylbenzenesulfonyl chloride

[0260] ##STR00119##

[0261] To a solution of 5-bromo-2,3-dimethylaniline (700 mg, 3.16 mmol) in concentrated HCl (4.0 mL) and AcOH (8.0 mL) was added NaNO.sub.2 (275 mg, 3.79 mmol) in water (2 mL) dropwise at ?15? C. and the mixture was stirred for 30 min to prepare a diazonium salt. In the meanwhile, AcOH (8.0 mL) was bubbled with SO.sub.2 (g) for 15 min, then CuCl (99 mg, 0.95 mmol) was added. SO.sub.2 was kept bubbled until a fine suspension was obtained. The suspension was cooled to 5? C. then added to the aforementioned diazonium solution in portions. The mixture was warmed to room temperature, stirred for 2 h then cooled to 0? C. The reaction was quenched with iced water (8 mL) and extracted with EtOAc (8 mL?2). The combined organic layer was washed with saturated NaHCO.sub.3 (10 mL?2) and water (20 mL), dried over anhydrous Na.sub.2SO.sub.4 then filtered. The filtrate was concentrated under reduced pressure and the crude (600 mg) was used in step 3 without further purification.

Step 3: 5-bromo-N,2,3-trimethylbenzemesulfonamide

[0262] ##STR00120##

[0263] To a solution of 5-bromo-2,3-dimethylbenzenesulfonyl chloride (600 mg, 1.056 mmol) in pyridine (4.0 mL) was added methylamine in THF (2 M, 0.63 mL, 1.26 mmol) and the mixture was stirred for 2 h at room temperature. The mixture was concentrated and triturated with water (5 mL). The mixture was filtered and the filtrate was discarded. The filter cake was rinsed with DCM (5 mL?2) and the filtrate was concentrated under reduced pressure to give the title compound (300 mg, 34% over 2 steps). LC-MS (M+H).sup.+=278.0.

Step 4: N,2,3-trimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide

[0264] ##STR00121##

[0265] The title compound (227 mg, 68%) was prepared in a manner similar to that in Example A7 step 2 from 5-bromo-N,2,3-trimethylbenzemesulfonamide and BPD. LC-MS (M+H).sup.+=326.1.

Step 5: 5-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-N,2,3-trimethylbenzemesulfonamide

[0266] Example A8 (7.3 mg, 9%) was prepared in a manner similar to that in Example A1 step 7 from N,2,3-trimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide and 5-bromo-3-(1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yloxy)pyrazin-2-amine. .sup.1H NMR (300 MHz, DMSO-d6) ? 8.27 (s, 1H), 8.13 (s, 1H), 8.09 (s, 1H), 7.91 (s, 1H), 7.60 (s, 1H), 7.48 (s, 1H), 6.80 (s, 2H), 4.17-4.05 (m, 1H), 2.90-2.76 (m, 2H), 2.49-2.41 (m, 6H), 2.35 (s, 3H), 2.20 (s, 3H), 2.11-1.91 (m, 6H). LC-MS (M+H).sup.+=472.3.

Example A9

3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methyl-N-(2-(piperidin-1-yl)ethyl)benzenesulfonamide

[0267] ##STR00122##

Step 1: 3-bromo-5-methyl-N-(2-(piperidin-1-yl)ethyl)benzenesulfonamide

[0268] ##STR00123##

[0269] P The titled compound (209 mg, 55%) was prepared in a manner similar to that in Example A2 step 2 from 3-bromo-5-methylbenzenesulfonyl chloride and 2-(piperidin-1-yl)ethan-1-amine. LC-MS (M+H).sup.+=361.1.

Step 2: 3-methyl-N-(2-(piperidin-1-yl)ethyl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide

[0270] ##STR00124##

[0271] The titled compound (117 mg, 49%) was prepared in a manner similar to that in Example A1 step 6 from 3-bromo-5-methyl-N-(2-(piperidin-1-yl)ethyl)benzenesulfonamide and BPD. LC-MS (M+H).sup.+=409.2.

Step 3: 3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methyl-N-(2-(piperidin-1-yl)ethyl)benzenesulfonamide

[0272] Example A9 (22 mg, 17%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-(1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yloxy)pyrazin-2-amine and 3-methyl-N-(2-(piperidin-1-yl)ethyl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide. .sup.1H NMR (400 MHz, DMSO-d.sub.6) ? 8.33 (s, 1H), 8.13 (s, 1H), 8.06 (s, 1H), 7.93 (s, 1H), 7.60 (s, 1H), 7.52 (s, 1H), 7.45 (s, 1H), 6.90 (s, 2H), 4.17-4.07 (m, 1H), 2.91-2.82 (m, 4H), 2.42 (s, 3H), 2.29-2.12 (m, 9H), 2.12-1.92 (m, 6H), 1.43-1.34 (m, 4H), 1.34-1.25 (m, 2H). LC-MS (M+H).sup.+=555.2.

Example A10

3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-N-(2-cyanoethyl)-5-methylbenzenesulfonamide

[0273] ##STR00125##

Step 1: 3-bromo-N-(2-cyanoethyl)-5-methylbenzenesulfonamide

[0274] ##STR00126##

[0275] A solution of 3-bromo-5-methylbenzenesulfonyl chloride (0.50 g, 1.85 mmol), 3-aminopropanenitrile (0.13 g, 1.85 mmol) and triethylamine (0.37 g, 3.7 mmol) in DCM (50 mL) was stirred at room temperature overnight. The mixture was removed under reduced pressure and the residue was purified by silica gel chromatograph (PE/EtOAc=5/l to 1/l) to give the title compound (0.38 g, 59%). LCMS (M+H).sup.+=303, 305.

Step 2: N-(2-cyanoethyl)-3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide

[0276] ##STR00127##

[0277] A mixture of 3-bromo-N-(2-cyanoethyl)-5-methylbenzenesulfonamide (0.37 g, 1.22 mmol), BPD (0.37 g, 1.46 mmol), Pd(dppf)Cl.sub.2 (53.5 mg, 0.073 mmol) and AcOK (0.24 g, 2.43 mmol) in dioxane (15 mL) was heated to reflux overnight under nitrogen. The mixture was cooled to room temperature and diluted with EtOAc (20 mL). The mixture was washed with brine (30 mL), and the aqueous layer was extracted with EtOAc (20 mL). The combined organic layer was dried over Na.sub.2SO.sub.4, filtered and concentrated to give the title compound (0.40 g, 93.6%). LC-MS (M+H).sup.+=351.1.

Step 3: 3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-N-(2-cyanoethyl)-5-methylbenzenesulfonamide

[0278] Example A10 (70 mg, 25%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and N-(2-cyanoethyl)-3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide. .sup.1H NMR (400 MHz, DMSO-d6) ? 8.33 (s, 1H), 8.12 (s, 1H), 8.08-7.99 (m, 2H), 7.94 (s, 1H), 7.59 (s, 1H), 7.52 (s, 1H), 6.89 (s, 2H), 4.18-4.16 (m, 1H), 3.05-2.95 (m, 2H), 2.92-2.83 (m, 2H), jo 2.67-2.60 (m, 2H), 2.42 (s, 3H), 2.21 (s, 3H), 2.13-1.95 (m, 6H). LCMS (M+H).sup.+=497.4.

Example A11

N-(1-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylphenyl)cyclopropyl)methanesulfonamide

[0279] ##STR00128##

Step 1: 1-(3-bromo-5-methylphenyl)cyclopropan-1-amine

[0280] ##STR00129##

[0281] To a solution of 3-bromo-5-methylbenzonitrile (9.50 g, 48.5 mmol) and Ti(Oi-Pr).sub.4 (16.1 g, 56.6 mmol) in Et.sub.2O (200 mL) was added ethylmagnesium bromide in Et.sub.2O (3 M, 35.7 mL, 107 mmol) At ?70? C. and the mixture was stirred for 10 min. The mixture was warmed to room temperature within 1 h, and then BF.sub.3Et.sub.2O (12.3 mL, 86.5 mmol) was added. After 1 h, HCl (30 mL, 1 N) and Et.sub.2O (100 mL) was added. Then aqueous NaOH (40 mL, 10%) was added and the mixture was extracted with ether (100 mL?3). The combined organic layer was dried over Na.sub.2SO.sub.4 and filtered. The filtrate was concentrated under reduced pressure and the residue was purified by silica gel chromatography (MeOH in DCM, 0% to 10%) to give the title compound (5.1 g, 44%). .sup.1H NMR (300 MHz, DMSO-d6) ? 7.41 (s, 1H), 7.32 (s, 1H), 7.17 (s, 1H), 2.28 (s, 2H), 1.31-1.08 (m, 4H).

Step 2: N-(1-(3-bromo-5-methylphenyl)cyclopropyl)methanesulfonamide

[0282] ##STR00130##

[0283] To a stirred solution of 1-(3-bromo-5-methylphenyl)cyclopropan-1-amine (1.0 g, 4.2 mmol) and triethylamine (1275 mg, 12.6 mmol) in acetonitrile (20 mL) was added MsCl (722 mg, 6.302 mmol) at 0? C. The mixture was stirred for overnight at room temperature then at 80? C. for 2 h. The mixture was cooled to room temperature and concentrated under reduced pressure. The residue was purified by silica gel chromatography (DCM/MeOH=15:1) to give the title compound (1.2 g, 89%). .sup.1H NMR (300 MHz, CDCl.sub.3) ? 7.36 (s, 1H), 7.20 (s, 1H), 7.16 (s, 1H), 6.09 (s, 1H), 2.59 (s, 3H), 2.30 (s, 3H), 1.42-1.30 (m, 2H), 1.17-1.09 (m, 2H).

Step 3: N-(1-(3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclopropyl)methanesulfonamide

[0284] ##STR00131##

[0285] The title compound (450 mg, 46%) was prepared in a manner similar to that in Example A1 step 6 from N-(1-(3-bromo-5-methylphenyl)cyclopropyl)methanesulfonamide and BPD. LC-MS (M+NH.sub.4)+=369.0.

Step 4: N-(1-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylphenyl)cyclopropyl)methanesulfonamide

[0286] Example A11 (23 mg, 17%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and N-(1-(3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclopropyl)methanesulfonamide. .sup.1H NMR (300 MHz, DMSO-d6) ? 8.22 (s, 2H), 8.14 (s, 1H), 7.66 (s, 1H), 7.57 (s, 1H), 7.50 (s, 1H), 7.15 (s, 1H), 6.72 (s, 2H), 4.19-4.07 (m, 1H), 2.91-2.81 (m, 2H), 2.51 (s, 3H), 2.31 (s, 3H), 2.18 (s, 3H), 2.10-1.91 (m, 6H), 1.29-1.20 (m, 2H), 1.21-1.06 (m, 2H). LC-MS (M+H).sup.+=498.3.

Example A12

N-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylphenethyl)methanesulfonamide

[0287] ##STR00132##

Step 1: 2-(3-bromo-5-methylphenyl)ethanamine hydrochloride

[0288] ##STR00133##

[0289] To a stirred solution of 2-(3-bromo-5-methylphenyl)acetonitrile (378 mg, 1.81 mmol) in MeOH (5 mL) was added Boc.sub.2O (218 mg, 0.948 mmol), NiCl.sub.2.Math.6H.sub.2O (118 mg, 0.470 mmol) and NaBH.sub.4 (1109 mg, 27.8 mmol) under nitrogen at 0? C. The mixture was warmed to room temperature and stirred for 2 h. The mixture was concentrated under vacuum. The crude was dissolved in dioxane (10 mL) and HCl in dioxane (10 mL, 40 mmol, 4 M) was added. The resulting mixture was stirred for 3 h at room temperature. The mixture was concentrated under vacuum. The residue was triturated in ethyl acetate (3 mL). The precipitated was collected by filtration and rinsed with ethyl acetate (1 mL?3) to give the title compound (444 mg, 98%). LC-MS (M+H).sup.+=214.0.

Step 2: N-(3-bromo-5-methylphenethyl)methanesulfonamide

[0290] ##STR00134##

[0291] The title compound (334 mg, 64%) was prepared in a manner similar to that in Example A11 step 2 from 2-(3-bromo-5-methylphenyl)ethanamine hydrochloride and MsCl. LC-MS (M+H).sup.+=292.0.

Step 3: N-(3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenethyl)methanesulfonamide

[0292] ##STR00135##

[0293] The compound 3 (214 mg, 55%) was prepared in a manner similar to that in Example A1 step 6 from N-(3-bromo-5-methylphenethyl)methanesulfonamide and BPD. LC-MS (M+H).sup.+=340.2.

Step 4: N-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylphenethyl)methanesulfonamide

[0294] Example A12 (4.2 mg, 1%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and N-(3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenethyl)methanesulfonamide. .sup.1H NMR (400 MHz, DMSO-d6) ? 8.24 (s, 1H), 8.12 (s, 1H), 7.59 (s, 1H), 7.51 (s, 2H), 7.14 (t, J=5.8 Hz, 1H), 6.98 (s, 1H), 6.70 (s, 2H), 4.19-4.07 (m, 1H), 3.23-3.14 (m, 2H), 2.90-2.86 (m, 2H), 2.85 (s, 3H), 2.75 (t, J=7.6 Hz, 2H), 2.31 (s, 3H), 2.21 (s, 3H), 2.10-1.90 (m, 6H). LC-MS (M+H).sup.+=486.3.

Example A13

3-(5-amino-6-((1-(piperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-N,5-dimethylbenzenesulfonamide

[0295] ##STR00136##

[0296] Example A13 (27 mg, 19%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(piperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine hydrochloride and N,3-dimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide. .sup.1H NMR (400 MHz, DMSO-d6) ? 8.32 (s, 1H), 8.11 (s, 1H), 8.02 (s, 1H), 7.94 (s, 1H), 7.58 (s, 1H), 7.49 (m, 2H), 6.90 (s, 2H), 4.27-4.12 (m, 1H), 3.11-3.00 (m, 2H), 2.70-2.54 (m, 3H), 2.43 (s, 6H), 2.07-1.95 (m, 2H), 1.90-1.73 (m, 2H). LC-MS (M+H).sup.+=444.3.

Example A14

3-(5-amino-6-((1-((1R,3s,5S)-8-methyl-8-azabicyclo[3,2,1]octan-3-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-N,5-dimethylbenzenesulfonamide

[0297] ##STR00137##

Step 1: tert-butyl (1R,3s,5S)-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)-8-azabicyclo[3.2.1]octane-8-carboxylate

[0298] ##STR00138##

[0299] A solution of 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl-1H-pyrazole (1.5 g, 7.73 mmol), tert-butyl (1R,3r,5S)-3-hydroxy-8-azabicyclo[3.2.1]octane-8-carboxylate (2.1 g, 9.27 mmol), DIAD (2.24 g, 11.6 mmol) and PPh.sub.3 (3.0 g, 11.6 mmol) in THF (30 mL) was stirred at room temperature overnight under nitrogen. The solvent was removed and the residue was purified by silica gel chromatography (PE/EtOAc=10/1 to 5/1) to give the title compound (3.0 g, 95%). LCMS (M+H).sup.+=404.1.

Step 2: tert-butyl (1R,3s,5S)-3-(4-hydroxy-1H-pyrazol-1-yl)-8-azabicyclo[3.2.1]octane-8-carboxylate

[0300] ##STR00139##

[0301] The title compound (1.5 g, 69%) was prepared in the same manner which described in compound A1 step 1 from tert-butyl (1R,3s,5S)-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)-8-azabicyclo[3.2.1]octane-8-carboxylate. LCMS (M+H).sup.+=294.

Step 3: tert-butyl (1R,3s,5S)-3-(4-((3-amino-6-bromopyrazin-2-yl)oxy)-1H-pyrazol-1-yl)-8-azabicyclo[3.2.1]octane-8-carboxylate

[0302] ##STR00140##

[0303] The title compound (0.35 g, 66%) was prepared in the same manner which described in compound A1 step 2 from tert-butyl (1R,3s,5S)-3-(4-hydroxy-1H-pyrazol-1-yl)-8-azabicyclo[3.2.1]octane-8-carboxylate and 3,5-dibromopyrazin-2-amine. LCMS (M+H).sup.+=465, 467.

Step 4: 3-((1-((1R,3s,5S)-8-azabicyclo[3.2.1]octan-3-yl)-1H-pyrazol-4-yl)oxy)-5-bromopyrazin-2-amine hydrochloride

[0304] ##STR00141##

[0305] The title compound (0.30 g, 100%) was prepared in the same manner which described in compound A1 step 3 from tert-butyl (1R,3s,5S)-3-(4-((3-amino-6-bromopyrazin-2-yl)oxy)-1H-pyrazol-1-yl)-8-azabicyclo[3.2.1]octane-8-carboxylate. LCMS (M+H).sup.+=365, 367.

Step 5: 5-bromo-3-((1-((1R,3s,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine

[0306] ##STR00142##

[0307] The title compound (0.30 g, 99%) was prepared in the same manner which described in compound A1 step 4 from 3-((1-((1R,3s,5S)-8-azabicyclo[3.2.1]octan-3-yl)-1H-pyrazol-4-yl)oxy)-5-bromopyrazin-2-amine hydrochloride. LCMS (M+H)+=379, 381.

Step 6: 3-(5-amino-6-((1-((1R,3s,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-N,5-dimethylbenzenesulfonamide

[0308] Example A14 (33 mg, 25%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-((1R,3s,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and N,3-dimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide. .sup.1H NMR (400 MHz, DMSO-d6) ? 8.33 (s, 1H), 8.13 (s, 1H), 8.04 (s, 1H), 7.95 (s, 1H), 7.61-7.53 (m, 2H), 7.50 (s, 1H), 6.90 (s, 2H), 4.55-4.40 (m, 1H), 3.21 (s, 2H), 2.43 (s, 6H), 2.25 (s, 3H), 2.16-2.05 (m, 2H), 2.05-1.95 (m, 2H), 1.89-1.81 (m, 2H), 1.74-1.65 (m, 2H). LCMS (M+H).sup.+=484.4.

Example A15

3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-N-ethyl-5-methylbenzenesulfonamide

[0309] ##STR00143##

Step 1: 3-bromo-N-ethyl-5-methylbenzenesulfonamide

[0310] ##STR00144##

[0311] A solution of 3-bromo-5-methylbenzenesulfonyl chloride (2.67 g, 10 mmol), ethylamine hydrochloride (1.62 g, 20 mmol) and TEA (3.03 g, 30 mmol) in DCM (50 mL) was stirred at room temperature for overnight. The mixture was concentrated and the crude was purified by silica gel chromatograph (PE/EtOAc=20/1 to 5/1) to give the title compound (0.85 g, 31%). LCMS (M+H).sup.+=278, 280.

Step 2: N-ethyl-3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide

[0312] ##STR00145##

[0313] A mixture of 3-bromo-N-ethyl-5-methylbenzenesulfonamide (850 mg, 3.0 mmol), BPD (762 mg, 3.0 mmol), Pd(dppf)Cl.sub.2.Math.DCM (123 mg, 0.15 mmol) and AcOK (882 mg, 9.0 mmol) in dioxane (15 mL) was heated to reflux under nitrogen for overnight. The mixture was cooled to room temperature filtered. The filtrate was concentrated under reduced pressure to give the title compound (810 mg, 83%). LC-MS (M+H).sup.+=326.3.

Step 3: 3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-N-ethyl-5-methylbenzenesulfonamide

[0314] Example A15 (48 mg, 34%) was prepared in a manner similar to that in Example A1 step 7 from N-ethyl-3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide and 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine. .sup.1H NMR (400 MHz, DMSO-d6) 8.31 (s, 1H), 8.11 (s, 1H), 8.02 (s, 1H), 7.92 (s, 1H), 7.60 (s, 1H), 7.50 (s, 2H), 6.90 (s, 2H), 4.20-4.05 (m, 1H), 2.92-2.85 (m, 2H), 2.83-2.75 (m, 2H), 2.42 (s, 3H), 2.22 (s, 3H), 2.12-1.94 (m, 6H), 0.98 (t, J=7.2 Hz, 3H). LCMS (M+H).sup.+=472.4.

Example A16

3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-isopropoxy-N-methylbenzenesulfonamide; formic acid

[0315] ##STR00146##

Step 1: 1-bromo-3-isopropoxy-5-nitrobenzene

[0316] ##STR00147##

[0317] A mixture of 3-bromo-5-nitrophenol (5.45 g, 25 mmol) and 2-iodopropane (8.5 g, 50 mmol), K.sub.2CO.sub.3 (6.9 g, 50 mmol) in DMF (50 mL) was stirred at room temperature overnight. Water (150 mL) was added and the mixture was extracted with EtOAc (150 mL). The organic layer was dried over Na.sub.2SO.sub.4 and filtered. The filtrate was concentrated to get the title compound (6.3 g, 97%).

Step 2: 3-bromo-5-isopropoxyaniline

[0318] ##STR00148##

[0319] The title compound (4.8 g, 86%) was prepared in a manner similar to that in Example A8 step 1 from 1-bromo-3-isopropoxy-5-nitrobenzene. LC-MS (M+H).sup.+=230.2.

Step 3: 3-bromo-5-isopropoxybenzenesulfonyl chloride

[0320] ##STR00149##

[0321] The title compound (4.6 g, 71%) was prepared in a manner similar to that in Example A8 step 2 from 3-bromo-5-isopropoxyaniline.

Step 4: 3-bromo-5-isopropoxy-N-methylbenzenesulfonamide

[0322] ##STR00150##

[0323] The title compound (584 mg, 24%) was prepared in a manner similar to that in Example A8 step 3 from 3-bromo-5-isopropoxybenzenesulfonyl chloride. LCMS (M+H).sup.+=308, 310.

Step 5: 3-isopropoxy-N-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide

[0324] ##STR00151##

[0325] The title compound (600 mg, 96%) was prepared in a manner similar to that in Example A1 step 6 from 3-bromo-5-isopropoxy-N-methylbenzenesulfonamide and BPD. LC-MS (M+H).sup.+=356.2.

Step 6: 3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-isopropoxy-N-methylbenzenesulfonamide; formic acid

[0326] Example A16 (20 mg, 37%) was prepared in a manner similar to that in Example A1 step 7 from 3-isopropoxy-N-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide and 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine. .sup.1H NMR (400 MHz, DMSO-d6) 8.33 (s, 1H), 8.17 (s, 1H), 8.09 (s, 1H), 7.77 (s, 1H), 7.58 (d, J=4.4 Hz, 2H), 7.45 (s, 1H), 7.14 (s, 1H), 6.92 (s, 2H), 4.78-4.64 (m, 1H), 4.15-4.05 (s, 1H), 2.95-2.85 (m, 2H), 2.43 (d, J=4.8 Hz, 3H), 2.23 (s, 3H), 2.13-1.96 (m, 6H), 1.31 (d, J=6.0 Hz, 6H). LCMS (M+H).sup.+=502.4.

Example A17

5-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-N-(2-(dimethylamino)ethyl)-2,3-dimethylbenzamide

[0327] ##STR00152##

Step 1: 5-bromo-N-(2-(dimethylamino)ethyl)-2,3-dimethylbenzamide

[0328] ##STR00153##

[0329] The title compound (400 mg, 89%) was prepared in a manner similar to that in Example A3 step 1 from 5-bromo-2,3-dimethylbenzoic acid and (2-aminoethyl)dimethylamine. LC-MS (M+H).sup.+=301.2.

Step 2: N-(2-(dimethylamino)ethyl)-2,3-dimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide

[0330] ##STR00154##

[0331] The title compound (185 mg, 47%) was prepared in a manner similar to that in Example A1 step 6 from 5-bromo-N-(2-(dimethylamino)ethyl)-2,3-dimethylbenzamide and BPD. LC-MS (M+H).sup.+=347.2.

Step 3: 5-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-N-(2-(dimethylamino)ethyl)-2,3-dimethylbenzamide

[0332] Example A17 (26 mg, 21%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and N-(2-(dimethylamino)ethyl)-2,3-dimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide. .sup.1H NMR (400 MHz, DMSO-d6) ? 8.27-8.19 (m, 2H), 8.09 (s, 1H), 7.69 (s, 1H), 7.60 (s, 1H), 7.55 (s, 1H), 6.70 (s, 2H), 4.19-4.07 (m, 1H), 3.39-3.27 (m, 4H), 2.96-2.87 (m, 2H), 2.30-2.23 (m, 12H), 2.20 (s, 3H), 2.19-2.05 (m, 2H), 2.08-1.93 (m, 4H). LC-MS (M+H).sup.+=493.4.

Example A18

5-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-3-fluoro-N,2-dimethylbenzenesulfonamide

[0333] ##STR00155##

Step 1: 5-bromo-3-fluoro-2-methylaniline

[0334] ##STR00156##

[0335] 5-bromo-1-fluoro-2-methyl-3-nitrobenzene (9.96 g, 42.6 mmol) and iron powder (11.9 g, 213 mmol) was added to a mixture of concentrated HCl (10 mL), ethanol (100 mL) and water (2 mL). The mixture was heated to reflux for 1 h, then cooled to room temperature. The mixture was filtered and the filtrate was concentrated under reduced pressure. The crude was partitioned between water (50 mL) and EtOAc (50 mL). The organic was separated, dried over Na.sub.2SO.sub.4 and filtered. The filtrate was concentrated under reduced pressure and the crude was purified by silica gel chromatography (PE/EtOAc=10:1) to give the title compound (3.5 g, 40%). LC-MS (M+H).sup.+=203.9, 205.9.

Step 2: 5-bromo-3-fluoro-N,2-dimethylbenzenesulfonamide

[0336] ##STR00157##

[0337] The title compound (1.0 g, 36%) was prepared in a manner similar to that in Example A2 step 1 and step 2 from 5-bromo-3-fluoro-2-methylaniline. LC-MS (M+H).sup.+=281.9 283.9.

Step 3: 3-fluoro-N,2-dimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide

[0338] ##STR00158##

[0339] The title compound (400 mg, 100%) was prepared in a manner similar to that in Example A1 step 6 from 5-bromo-3-fluoro-N,2-dimethylbenzenesulfonamide and BPD. LC-MS (M+H).sup.+=330.1.

Step 4: 5-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-3-fluoro-N,2-dimethylbenzenesulfonamide

[0340] Example A18 (70 mg, 26%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and 3-fluoro-N,2-dimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide. .sup.1H NMR (400 MHz, DMSO-d6) ? 8.35 (s, 1H), 8.12 (s, 1H), 8.08 (s, 1H), 7.91 (d, J=10.9 Hz, 1H), 7.68 (s, 1H), 7.61 (s, 1H), 6.96 (s, 2H), 4.10 (dd, J=9.8, 4.8 Hz, 1H), 2.86 (d, J=10.4 Hz, 2H), 2.47 (s, 3H), 2.45 (s, 3H), 2.21 (s, 3H), 2.09-1.94 (m, 6H). LC-MS (M+H).sup.+=476.1.

Example A19

N-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylbenzyl)methanesulfonamide

[0341] ##STR00159##

Step 1: 1-(4-bromo-2,6-dimethylphenyl)methanamine

[0342] ##STR00160##

[0343] At 0? C., to a solution of 4-bromo-2,6-dimethylbenzonitrile (900 mg, 4.07 mmol) in THF (20 mL) was added BH.sub.3-THF (1 M, 20 mL, 20 mmol) under nitrogen. The resulting mixture was stirred for 16 h at 80? C. under nitrogen atmosphere. The mixture was cooled to 0? C. and quenched by the addition of MeOH (5 mL) and ice water (5 mL). The mixture was then warmed to 70? C. and stirred for 2 h. The mixture was concentrated under reduced pressure and the residue was purified by silica gel chromatography (MeOH in DCM from 0% to 13% gradient) to give the title compound (868 mg, 99%). LC-MS (M+H).sup.+=214.

Step 2: N-(4-bromo-2,6-dimethylbenzyl)methanesulfonamide

[0344] ##STR00161##

[0345] The title compound (504 mg, 85%) was prepared in a manner similar to that in Example A11 step 2 from 1-(4-bromo-2,6-dimethylphenyl)methanamine. LC-MS (M+H).sup.+=292.0.

Step 3: N-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)methanesulfonamide

[0346] ##STR00162##

[0347] The title compound (418 mg, 80%) was prepared in a manner similar to that in Example A1 step 6 from N-(4-bromo-2,6-dimethylbenzyl)methanesulfonamide and BPD. LC-MS (M+NH.sub.4).sup.+=357.2.

Step 4; N-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylbenzyl)methanesulfonamide

[0348] Example A19 (25 mg, 13%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and N-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)methanesulfonamide. .sup.1H NMR (400 MHz, DMSO-d6) ? 8.22 (s, 1H), 8.10 (s, 1H), 7.57 (s, 1H), 7.49 (s, 2H), 7.08-6.99 (m, 1H), 6.70 (s, 2H), 4.18-4.04 (m, 3H), 2.93 (s, 3H), 2.89-2.79 (m, 2H), 2.36 (s, 6H), 2.19 (s, 3H), 2.11-1.89 (m, 6H). LC-MS (M+H).sup.+=486.1.

Example A20

N-(1-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylphenyl)cyclopropyl)benzenesulfonamide

[0349] ##STR00163##

Step 1: tert-butyl (1-(3-bromo-5-methylphenyl)cyclopropyl)carbamate

[0350] ##STR00164##

[0351] To a stirred solution of 1-(3-bromo-5-methylphenyl)cyclopropan-1-amine (1.50 g, 6.30 mmol) and triethylamine (2.77 mL, 27.3 mmol) in DCM (15 mL) was added Boc.sub.2O (1.85 mL, 8.45 mmol) in portions at 0? C. The mixture was warmed to room temperature and stirred for 3 h, then diluted with water (60 mL). The mixture was extracted with DCM (60 mL?3). The combined organic layer was washed with brine, dried over Na.sub.2SO.sub.4 and filtered. The filtrate was concentrated under reduced pressure to give the title compound (1.53 g, 75%).

Step 2: tert-butyl (1-(3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclopropyl)carbamate

[0352] ##STR00165##

[0353] The title compound (1.55 g, 94%) was prepared in a manner similar to that in Example A1 step 6 from tert-butyl (1-(3-bromo-5-methylphenyl)cyclopropyl)carbamate and BPD. LC-MS (M-t-Bu).sup.+=318.2.

Step 3: tert-butyl (1-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylphenyl)cyclopropyl)carbamate

[0354] ##STR00166##

[0355] The title compound (688 mg, 81%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and tert-butyl (1-(3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclopropyl)carbamate. LC-MS (M+H).sup.+=520.3.

Step 4: 5-(3-(1-aminocyclopropyl)-5-methylphenyl)-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine

[0356] ##STR00167##

[0357] To a stirred solution of tert-butyl (1-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylphenyl)cyclopropyl)carbamate (688 mg, 1.33 mmol) in MeOH (20 mL) was added HCl in MeOH (3 M, 4 mL, 12 mmol) dropwise at room temperature. After 2 h, the mixture was concentrated under vacuum. The residue was partitioned between saturated NaHCO.sub.3 (30 mL) and DCM (30 mL). The organic layer was separated, dried over Na.sub.2SO.sub.4 and filtered. The filtrate was concentrated under reduced pressure and residue was purified by silica gel chromatography (DCM/MeOH=10:1) to give the title compound (450 mg, 81%). LC-MS (M+H).sup.+=420.2.

Step 5: N-(1-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylphenyl)cyclopropyl)benzenesulfonamide

[0358] To a solution of 5-(3-(1-aminocyclopropyl)-5-methylphenyl)-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine (77 mg, 0.185 mmol) in pyridine (5 mL) was added benzenesulfonyl chloride (137 mg, 0.74 mmol) at room temperature under nitrogen. After 4 h, the mixture was concentrated under reduced pressure and the crude was purified by prep-HPLC (7.0 mg, 7%) to give Example A20. .sup.1H NMR (400 MHz, DMSO-d6) ? 8.70 (br s, 1H), 8.15 (s, 1H), 8.08 (s, 1H), 7.59 (s, 1H), 7.57-7.51 (m, 2H), 7.43-7.27 (m, 5H), 6.84 (s, 1H), 6.70 (s, 2H), 4.22-4.09 (m, 1H), 2.90-2.83 (m, 2H), 2.19 (s, 3H), 2.14 (s, 3H), 2.10-1.94 (m, 6H), 1.17-1.11 (m, 2H), 1.06-1.00 (m, 2H). LC-MS (M+H).sup.+=560.2.

Example A21

4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-N-methoxy-2,6-dimethylbenzamide

[0359] ##STR00168##

[0360] A solution of 4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylbenzoic acid (240 mg, 0.568 mmol), O-methylhydroxylamine hydrochloride (71 mg, 0.852 mmol), HATU (324 mg, 0.852 mmol) and DIPEA (220 mg, 1.70 mmol) in DMF (10 mL) was stirred at room temperature overnight. The mixture was concentrated in vacuo and the crude was purified by silica gel chromatography to give Example A21 (20 mg, 8%). .sup.1H NMR (400 MHz, DMSO-d6) ? 11.39 (s, 1H), 8.26 (s, 1H), 8.11 (s, 1H), 7.59 (s, 1H), 7.53 (s, 2H), 6.77 (s, 2H), 4.13 (s, 1H), 3.73 (s, 3H), 2.85 (d, J=10.6 Hz, 2H), 2.26 (s, 6H), 2.20 (s, 3H), 2.09-1.96 (m, 6H). LC-MS (M+H).sup.+=452.0.

Example A22

3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-N-methyl-5-(methylamino)benzenesulfonamide

[0361] ##STR00169##

Step 1: 3-bromo-N-methyl-5-nitroaniline

[0362] ##STR00170##

[0363] To mixture of 1-bromo-3-fluoro-5-nitrobenzene (4.0 g, 17.3 mmol) and methylamine hydrochloride (2.33 g, 34.5 mmol) in DMAC (30 mL) was added Cs.sub.2CO.sub.3 (6.0 g, 17.5 mmol) at room temperature. The mixture was warmed to 80? C., stirred for 2 h then cooled to room temperature. The mixture was extracted with EtOAc (100 mL?3). The combined organic layer was washed with brine (20 mL?3), dried over anhydrous Na.sub.2SO.sub.4 and filtered. The filtrate was concentrated under reduced pressure and the residue was purified by silica gel column chromatography (PE/EtOAc=5:1) to give the title compound (3.72 g, 93%). LC-MS (M+H).sup.+=231.0.

Step 2: 5-bromo-N.SUP.1.-methylbenzene-1,3-diamine

[0364] ##STR00171##

[0365] The title compound (3.0 g, 93%) was prepared in a manner similar to that in Example A8 step 1 from 3-bromo-N-methyl-5-nitroaniline. LC-MS (M+H).sup.+=201.1.

Step 3: 3-bromo-5-(methylamino)benzenesulfonyl chloride

[0366] ##STR00172##

[0367] The title compound (562 mg, 40%) was prepared in a manner similar to that in Example A8 step 2 from 5-bromo-N.sup.1-methylbenzene-1,3-diamine. LC-MS (M+H).sup.+=283.9.

Step 4: 3-bromo-N-methyl-5-(methylamino)benzenesulfonamide

[0368] ##STR00173##

[0369] The title compound (200 mg, 36%) was prepared in a manner similar to that in Example A8 step 3 from 3-bromo-5-(methylamino)benzenesulfonyl chloride. LC-MS (M+H).sup.+=278.9.

Step 5: N-methyl-3-(methylamino)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide

[0370] ##STR00174##

[0371] The title compound (110 mg, 94%) was prepared in a manner similar to that in Example A1 step 6 from 3-bromo-N-methyl-5-(methylamino)benzenesulfonamide and BPD. LC-MS (M+H).sup.+=327.2.

Step 6: 33-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-N-methyl-5-(methylamino)benzenesulfonamide

[0372] Example A22 (8 mg, 8%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and N-methyl-3-(methylamino)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide. .sup.1H NMR (400 MHz, DMSO-d6) ? 8.20 (s, 1H), 8.08 (s, 1H), 7.62 (s, 1H), 7.40-7.34 (m, 1H), 7.33-7.27 (m, 1H), 7.19-7.15 (m, 1H), 6.88-6.84 (m, 1H), 6.82 (s, 2H), 6.26-6.19 (m, 1H), 4.15-4.03 (m, 1H), 2.90-2.80 (m, 2H), 2.75 (d, J=4.9 Hz, 3H), 2.42 (d, J=4.9 Hz, 3H), 2.20 (s, 3H), 2.10-1.88 (m, 6H). LC-MS (M+H).sup.+=473.0.

Example A23

3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-N-methyl-5-(pyrrolidin-1-yl)benzenesulfonamide

[0373] ##STR00175##

Step 1: 1-(3-bromo-5-nitrophenyl)pyrrolidine

[0374] ##STR00176##

[0375] The title compound (4.37 g, 93%) was prepared in a manner similar to that in Example A22 step 1 from 1-bromo-3-fluoro-5-nitrobenzene and pyrrolidine. LC-MS (M+H).sup.+=271.1.

Step 2: 3-bromo-5-(pyrrolidin-1-yl)aniline

[0376] ##STR00177##

[0377] The title compound (3.18 g, 82%) was prepared in a manner similar to that in Example A8 step 1 from 1-(3-bromo-5-nitrophenyl)pyrrolidine. LC-MS (M+H).sup.+=241.1.

Step 3: 3-bromo-5-(pyrrolidin-1-yl)benzenesulfonyl chloride

[0378] ##STR00178##

[0379] The title compound (208 mg, 24%) was prepared in a manner similar to that in Example A8 step 2 from 3-bromo-5-(pyrrolidin-1-yl)aniline. LC-MS (M+H).sup.+=323.9.

Step 4: 3-bromo-N-methyl-5-(pyrrolidin-1-yl)benzenesulfonamide

[0380] ##STR00179##

[0381] The title compound (145 mg, 88%) was prepared in a manner similar to that in Example A8 step 3 from 3-bromo-5-(pyrrolidin-1-yl)benzenesulfonyl chloride. LC-MS (M+H).sup.+=319.0.

Step 5: N-methyl-3-(pyrrolidin-1-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide

[0382] ##STR00180##

[0383] The title compound (149 mg, 89%) was prepared in a manner similar to that in Example A1 step 6 from 3-bromo-N-methyl-5-(pyrrolidin-1-yl)benzenesulfonamide and BPD. LC-MS (M+H).sup.+=367.3.

Step 6: 3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-N-methyl-5-(pyrrolidin-1-yl)benzenesulfonamide

[0384] Example A23 (6 mg, 6%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and N-methyl-3-(pyrrolidin-1-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide. .sup.1H NMR (400 MHz, DMSO-d6) ? 8.27 (s, 1H), 8.12 (s, 1H), 7.59 (s, 1H), 7.43 (s, 1H), 7.35-7.30 (m, 1H), 7.21-7.16 (m, 1H), 6.84 (s, 2H), 6.80-6.77 (m, 1H), 4.15-4.03 (m, 1H), 3.33-3.27 (m, 4H), 2.91-2.83 (m, 2H), 2.42 (d, J=5.0 Hz, 3H), 2.21 (s, 3H), 2.10-1.90 (m, 10H). LC-MS (M+H).sup.+=513.3.

Example A24

3-(5-amino-6-((1-(1-cyclopropylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-N,5-dimethylbenzenesulfonamide

[0385] ##STR00181##

Step 1: 5-bromo-3-((1-(1-cyclopropylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine

[0386] ##STR00182##

[0387] To a stirred solution of 5-bromo-3-((1-(piperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine (100 mg, 0.286 mmol) and (1-ethoxycyclopropyl)trimethylsilane (105 mg, 0.572 mmol) in MeOH (2 mL) and THF (2.00 mL) was added AcOH (0.30 mL) and NaBH.sub.3CN (57 mg, 0.86 mmol) at room temperature and the mixture was heated to 60? C. under nitrogen for overnight. The mixture was cooled to room temperature and concentrated under reduced pressure. The residue was purified by silica gel chromatography (DCM/MeOH=6:1) to give the title compound (70 mg, 60%). LC-MS (M+H).sup.+=381.0.

Step 2: 3-(5-amino-6-((1-(1-cyclopropylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-N,5-dimethylbenzenesulfonamide

[0388] Example A24 (27 mg, 26%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-cyclopropylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and N,3-dimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide. .sup.1H NMR (300 MHz, DMSO-4) ? 8.31 (s, 1H), 8.11 (s, 1H), 8.00 (s, 1H), 7.93 (s, 1H), 7.57 (s, 1H), 7.49 (s, 1H), 7.41-7.30 (m, 1H), 6.87 (s, 2H), 4.24-4.08 (m, 1H), 3.10-2.95 (m, 2H), 2.46-2.26 (m, 8H), 2.10-1.99 (m, 2H), 1.98-1.80 (m, 2H), 1.66 (s, 1H), 0.48-0.26 (m, 4H). LC-MS (M+H).sup.+=484.2.

Example A25

N-(l-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylphenyl)cyclopropyl)-2,2,2-trifluoroethane-1-sulfonamide

[0389] ##STR00183##

[0390] Example A25 (32 mg, 26%) was prepared in a manner similar to that in Example A20 step 5 from 5-(3-(1-aminocyclopropyl)-5-methylphenyl)-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and 2,2,2-trifluoroethanesulfonyl chloride. .sup.1H NMR (300 MHz, DMSO-d.sub.6) ? 8.92 (s, 1H), 8.23 (s, 1H), 8.16 (s, 1H), 7.62 (s, 1H), 7.59 (s, 1H), 7.53 (s, 1H), 7.15 (s, 1H), 6.75 (s, 2H), 4.23-4.07 (m, 1H), 4.07-3.89 (m, 2H), 2.95-2.81 (m, 2H), 2.33 (s, 3H), 2.22 (s, 3H), 2.15-1.94 (m, 6H), 1.39-1.29 (m, 2H), 1.28-1.13 (m, 2H). LC-MS (M+H).sup.+=566.3.

Example A26

1-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylbenzyl)-3-methylurea

[0391] ##STR00184##

Step 1: 1-(4-bromo-2,6-dimethylbenzyl)-3-methylurea

[0392] ##STR00185##

[0393] To a stirred solution of 1-(4-bromo-2,6-dimethylphenyl)methanamine (100 mg, 0.451 mmol) in DCM (20 mL) was added triethylamine (0.13 mL, 0.902 mmol) and triphosgene (45 mg, 0.144 mmol) at 0? C. After 3 h, methylamine in THF (2 M, 0.45 mL, 0.90 mmol) was added. The mixture was warmed to room temperature and stirred for overnight. The resulting mixture was diluted with water (20 mL) and extracted with DCM (20 mL?3). Combined organic layer was dried over anhydrous Na.sub.2SO.sub.4 and filtered. The filtrate was concentrated under reduced pressure jo and the residue was purified by silica gel chromatography (DCM/MeOH=8:1) to give the title compound (55 mg, 45%). LC-MS (M+H).sup.+=271.1.

Step 2: 1-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)-3-methylurea

[0394] ##STR00186##

The title compound (44 mg, 68%) was prepared in a manner similar to that in Example A1 step 6 from 1-(4-bromo-2,6-dimethylbenzyl)-3-methylurea and BPD. LC-MS (M+H).sup.+=319.3.

Step 3: 1-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylbenzyl)-3-methylurea

[0395] Example A26 (11 mg, 20%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and 1-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)-3-methylurea. .sup.1H NMR (300 MHz, DMSO-d6) ? 8.19 (s, 1H), 8.10 (s, 1H), 7.57 (s, 1H), 7.46 (s, 2H), 6.66 (s, 2H), 5.96-5.83 (m, 1H), 5.60-5.49 (m, 1H), 4.21-4.03 (m, 3H), 2.92-2.79 (m, 2H), 2.53 (d, J=4.6 Hz, 3H), 2.32 (s, 6H), 2.19 (s, 3H), 2.12-1.97 (m, 6H). LC-MS (M+H).sup.+=465.2.

Example A27

3-(5-amino-6-((1-(1-ethylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-N,5-dimethylbenzenesulfonamide

[0396] ##STR00187##

Step 1: 3-(5-amino-6-((1-(piperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-N,5-dimethylbenzenesulfonamide

[0397] The title compound (2.0 g, 99%) was prepared in a manner similar to that in Example A1 step 7 from N,3-dimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide and 5-bromo-3-((1-(piperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine. LC-MS (M+H).sup.+=444.1.

Step 2: 3-(5-amino-6-((1-(1-ethylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-N,5-dimethylbenzenesulfonamide

[0398] To a solution of 3-(5-amino-6-((1-(piperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-N,5-dimethylbenzenesulfonamide (400 mg, 0.898 mmol) and acetaldehyde (200 mg, 4.49 mmol) in DCM (3 mL) was added AcOH (55 mg, 0.898 mmol) at 0? C. The mixture was stirred for 1.5 h at 0? C. under nitrogen, then NaBH.sub.3CN (114 mg, 1.80 mmol) was added. After 1 h, the mixture was concentrated and the residue was purified by prep-HPLC to give Example A27 (53 mg, 12%). .sup.1H NMR (400 MHz, DMSO-d6) ? 8.32 (s, 1H), 8.12 (s, 1H), 8.02 (s, 1H), 7.94 (s, 1H), 7.59 (s, 1H), 7.49 (s, 1H), 7.46-7.40 (m, 1H), 6.90 (s, 2H), 4.18-4.08 (m, 1H), 3.01-2.90 (m, 2H), 2.45-2.40 (m, 6H), 2.39-2.30 (m, 2H), 2.10-1.92 (m, 6H), 1.02 (t, J=7.2 Hz, 3H). LC-MS (M+H).sup.+=472.1.

Example A28

3-(5-amino-6-((1-(1-(oxetan-3-ylmethyl)piperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-N, 5-dimethylbenzenesulfonamide

[0399] ##STR00188##

[0400] Example A28 (14 mg, 2% was prepared in a manner similar to that in Example A27 step 2 from 3-(5-amino-6-((1-(piperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-N,5-dimethylbenzenesulfonamide and oxetane-3-carbaldehyde. .sup.1H NMR (300 MHz, DMSO-d6) ? 8.30 (s, 1H), 8.10 (s, 1H), 8.01-7.98 (m, 1H), 7.91 (s, 1H), 7.56 (s, 1H), 7.47 (s, 1H), 7.41-7.34 (m, 1H), 6.89 (s, 2H), 4.67-4.57 (m, 2H), 4.25 (t, J=6.1 Hz, 2H), 4.18-4.02 (m, 1H), 3.23-3.08 (m, 1H), 2.91-2.78 (m, 2H), 2.68-2.60 (m, 2H), 2.44-2.37 (m, 6H), 2.15-1.81 (m, 6H). LC-MS (M+H).sup.+=514.2.

Example A29

4-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylphenyl)oxazolidin-2-ol

[0401] ##STR00189##

Step 1: 2-amino-2-(4-bromo-2,6-dimethylphenyl)acetonitrile

[0402] ##STR00190##

[0403] To a solution of 4-bromo-2,6-dimethylbenzaldehyde (5.0 g, 22.3 mmol) in MeOH (20 mL) was added NH.sub.3 in MeOH (7 M, 26 mL, 178 mmol) and Ti(Oi-Pr).sub.4 (7.67 g, 25.6 mmol) at room temperature under nitrogen. After 2 h, TMSCN (2.33 g, 22.3 mmol) was added dropwise. After 24 h, iced water (100 mL) was added. The solid was filtered off and the filter cake was rinsed with EtOAc (20 mL?3). The filtrate was extracted with EtOAc (300 mL?3). The combined organic layer was washed with brine (150 mL), dried over Na.sub.2SO.sub.4 and filtered. The filtrate was concentrated under reduced pressure and the residue was purified by silica gel chromatography (EtOAc:hexane=3:2) to give the title compound (2.07 g, 39%).

Step 2: amino(4-bromo-2,6-dimethylphenyl)acetic acid hydrochloride

[0404] ##STR00191##

[0405] To the 2-amino-2-(4-bromo-2,6-dimethylphenyl)acetonitrile (1.71 g, 7.15 mmol) was added aqueous HCl (6 M, 90 mL) then the mixture was heated to 105? C. for overnight. The mixture was cooled to room temperature, and the solvent was evaporated under reduced pressure to about one third of the original volume. The precipitate was collected by filtration and dried under vacuum to give the title compound (865 mg, 41%). LC-MS (M+H).sup.+=258.1.

Step 3: 2-amino-2-(4-bromo-2,6-dimethylphenyl)ethan-1-ol hydrochloride

[0406] ##STR00192##

[0407] To a solution of LiBH.sub.4 in THF (2.5 M, 7.6 mL, 7.540 mmol) was added TMSCl (1.72 g, 15.00 mmol) and amino (4-bromo-2,6-dimethylphenyl)acetic acid hydrochloride (779 mg, 2.65 mmol) at room temperature. After 12 h, the solution was cooled to 0? C. and MeOH (10 mL) and water (100 mL) was carefully added. After 15 min, saturated NaHCO.sub.3 (100 mL) was carefully added and the mixture was extracted with EtOAc (250 mL?3). The combined organic layer was washed with brine (100 mL), dried over Na.sub.2SO.sub.4 and filtered. The filtrate was concentrated under reduced pressure and the crude was purified by C18 chromatography (MeOH in 0.1% aqueous HCl) to give the title compound (370 mg, 50%). LC-MS (M+H).sup.+=244.0.

Step 4: 4-(4-bromo-2,6-dimethylphenyl)-1,3-oxazolidin-2-one

[0408] ##STR00193##

[0409] To a solution of 2-amino-2-(4-bromo-2,6-dimethylphenyl)ethan-1-ol hydrochloride (231 mg, 0.83 mmol) and triethylamine (303 mg, 2.85 mmol) in DCM (15 mL) was added triphosgene (148 mg, 0.47 mmol) in DCM (5 mL) dropwise at 0? C. under nitrogen. The mixture was warmed to room temperature and stirred for 3 h. Water (20 mL) was added and the mixture was extracted with DCM (80 mL?3). The combined organic layer was washed with brine (50 mL), dried over Na.sub.2SO.sub.4 and filtered. The filtrate was concentrated under reduced pressure and the residue was purified by silica gel chromatography (MeOH:DCM=1:9) to give the title compound (131 mg, 51%). LC-MS (M+H).sup.+=270.0.

Step 5: 4-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)oxazolidin-2-one

[0410] ##STR00194##

[0411] The compound 5 (125 mg, 94%) was prepared in a manner similar to that in Example A1 step 6 from 4-(4-bromo-2,6-dimethylphenyl)-1,3-oxazolidin-2-one and BPD. LC-MS (M+H).sup.+=318.3.

Step 6: 4-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylphenyl)oxazolidin-2-one

[0412] Example A29 (16 mg, 12%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and 4-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)oxazolidin-2-one. .sup.1H NMR (400 MHz, DMSO-d6) ? 8.25 (s, 1H), 8.12 (s, 1H), 7.96-7.91 (m, 1H), 7.59 (s, 1H), 7.51 (s, 2H), 6.73 (s, 2H), 5.47-5.37 (m, 1H), 4.77-4.68 (m, 1H), 4.20-4.07 (m, 2H), 2.91-2.82 (m, 2H), 2.37 (s, 6H), 2.22 (s, 3H), 2.05-1.91 (m, 6H). LC-MS (M+H).sup.+=464.1.

Example A30

3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-(tert-butyl)-N-methylbenzenesulfonamide

[0413] ##STR00195##

Step 1: 3-bromo-5-tert-butylbenzene-1-sulfonyl chloride

[0414] ##STR00196##

[0415] At ?78? C., to a solution of 1,3-dibromo-5-tert-butylbenzene (1.00 g, 3.25 mmol) in THF (15 mL) was added n-BuLi in hexanes (2.5 M, 0.2 mL, 3.83 mmol) dropwise under nitrogen. After 30 min, SO.sub.2 (g) was bubbled into the mixture for 1 h at the same temperature. The mixture was warmed to room temperature and stirred for overnight then concentrated under vacuum. To the crude was added DCM (15 mL) and NCS (457 mg, 3.25 mmol) at 0? C. The mixture was warmed to room temperature and stirred for 1 h. The mixture was filtered, and the filter cake was washed with DCM (50 mL?3). The filtrate was concentrated under reduced pressure to give the title compound (900 mg, crude).

Step 2: 3-bromo-5-tert-butyl-N-methylbenzenesulfonamide

[0416] ##STR00197##

[0417] The compound 1 (74 mg, 8% for 2 steps) was prepared in a manner similar to that in Example A8 step 3 from 3-bromo-5-tert-butylbenzene-1-sulfonyl chloride. LC-MS (M+H).sup.+=306.0.

Step 3: 3-tert-butyl-N-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide

[0418] ##STR00198##

[0419] The title compound (67 mg, 79%) was prepared in a manner similar to that in Example A1 step 6 from 3-bromo-5-tert-butyl-N-methylbenzenesulfonamide and BPD. LC-MS (M+H).sup.+=354.2.

Step 4: 3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-(tert-butyl)-N-methylbenzenesulfonamide

[0420] Example A30 (18 mg, 21%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and 3-tert-butyl-N-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide. .sup.1H NMR (300 MHz, DMSO-d6) ? 8.34 (s, 1H), 8.09 (s, 2H), 8.004-7.99 (m, 1H), 7.68-7.55 (m, 2H), 7.48-7.40 (m, 1H), 6.89 (s, 2H), 4.14-4.03 (m, 1H), 2.91-2.80 (m, 2H), 2.44-2.37 (m, 3H), 2.20 (s, 3H), 2.10-1.90 (m, 6H), 1.32 (s, 9H). LC-MS (M+H).sup.+=500.3.

Example A31

N-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylbenzyl)tetrahydro-2H-pyran-4-sulfonamide

[0421] ##STR00199##

Step 1: N-(4-bromo-2,6-dimethylbenzyl)tetrahydro-2H-pyran-4-sulfonamide

[0422] ##STR00200##

[0423] The title compound (123 mg, 48%) was prepared in a manner similar to that in Example A20 step 5 from 1-(4-bromo-2,6-dimethylphenyl)methanamine and oxane-4-sulfonyl chloride. LC-MS (M+H).sup.+=362.0.

Step 2: N-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)tetrahydro-2H-pyran-4-sulfonamide

[0424] ##STR00201##

[0425] The title compound (99 mg, 71%) was prepared in a manner similar to that in Example A1 step 6 from N-(4-bromo-2,6-dimethylbenzyl)tetrahydro-2H-pyran-4-sulfonamide and BPD. LC-MS (M+H).sup.+=410.2.

Step 3: N-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylbenzyl)tetrahydro-2H-pyran-4-sulfonamide

[0426] Example A31 (19 mg, 14%) was prepared in a manner similar to that in Example A1 step 7 from bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and N-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)tetrahydro-2H-pyran-4-sulfonamide. .sup.1H NMR (400 MHz, DMSO-d6) ? 8.23 (s, 1H), 8.12 (s, 1H), 7.59 (s, 1H), 7.50 (s, 2H), 7.28-7.20 (m, 1H), 6.70 (s, 2H), 4.20-4.10 (m, 3H), 3.99-3.91 (m, 2H), 2.94-2.84 (m, 2H), 2.38 (s, 6H), 2.25 (s, 3H), 2.19-2.09 (m, 2H), 2.04-1.93 (m, 4H), 1.92-1.82 (m, 2H), 1.71-1.57 (m, 2H). LC-MS (M+H).sup.+=556.4.

Example A32

N-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylbenzyl)cyclopropanesulfonamide

[0427] ##STR00202##

Step 1: N-(4-bromo-2,6-dimethylbenzyl)cyclopropanesulfonamide

[0428] ##STR00203##

[0429] The title compound (215 mg, 82%) was prepared in a manner similar to that in Example A20 step 5 from 1-(4-bromo-2,6-dimethylphenyl)methanamine and cyclopropanesulfonyl chloride. LC-MS (M+H).sup.+=318.0.

Step 2: N-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)cyclopropanesulfonamide

[0430] ##STR00204##

[0431] The title compound (119 mg, 71%) was prepared in a manner similar to that in Example A1 step 6 from N-(4-bromo-2,6-dimethylbenzyl)cyclopropanesulfonamide and BPD. LC-MS (M+NH.sub.4).sup.+=383.2.

Step 3: N-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylbenzyl)cyclopropanesulfonamide

[0432] Example A32 (8 mg, 6%) was prepared in a manner similar to that in Example A1 final step from bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and N-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)cyclopropanesulfonamide. .sup.1H NMR (300 MHz, DMSO-d.sub.6) ? 8.22 (s, 1H), 8.11 (s, 1H), 7.58 (s, 1H), 7.49 (s, 2H), 7.13-7.05 (m, 1H), 6.69 (s, 2H), 4.23-4.08 (m, 3H), 2.99-2.83 (m, 2H), 2.65-2.55 (m, 1H), 2.37 (s, 6H), 2.30-2.21 (m, 3H), 2.16-2.04 (m, 6H), 0.99-0.91 (m, 4H). LC-MS (M+H).sup.+=512.2.

Example A33

4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2-(difluoromethyl)-N-(2-(dimethylamino)ethyl)-6-methylbenzamide

[0433] ##STR00205##

Step 1: ethyl 4-(dibenzylamino)-2-(difluoromethyl)-6-methylbenzoate

[0434] ##STR00206##

[0435] A mixture of pentane-2,4-dione (15 g, 150 mmol), dibenzylamine (44.3 g, 225 mmol) and zinc acetate (1.38 g, 7.5 mmol) was stirred at 50? C. for 2 days under nitrogen. Ethyl 4,4-difluoro-3-oxobutanoate (24.9 g, 150 mmol) and AcOH (300 mL) was added and the mixture was stirred at 120? C. for 3 h under nitrogen.

[0436] The mixture was concentrated under reduced pressure and the residue was taken up in water (300 mL). The pH of the mixture was adjusted to 8 with saturated NaHCO.sub.3 and the mixture was extracted with EtOAc (300 mL?2). The combined organic layer was washed with brine (100 mL), dried over Na.sub.2SO.sub.4 and filtered. The filtrate was concentrated under reduced pressure and the crude was purified by silica gel chromatography (PE/EtOAc=10/1 to 5/1) to give the title compound (3.0 g, 5%). LCMS (M+H).sup.+=410.1.

Step 2: ethyl 4-amino-2-(difluoromethyl)-6-methylbenzoate

[0437] ##STR00207##

[0438] Pd/C (10% loading) was added to a solution of ethyl 4-(dibenzylamino)-2-(difluoromethyl)-6-methylbenzoate (3.0 g, 7.31 mmol) in EtOH (30 mL) and AcOH (15 mL) under nitrogen, then the system was flushed with hydrogen. The mixture was stirred at room temperature overnight. The solid was filtered off and the filtrate was concentrated under reduced pressure. The residue was taken up in water (50 mL) and the pH of the mixture was adjusted to 8 with saturated NaHCO.sub.3. The mixture was extracted with EtOAc (50 mL?2). The combined organic layer was washed with brine (30 mL), dried over Na.sub.2SO.sub.4 and filtered. The filtrate was concentrated under reduced pressure and the crude was purified by silica gel chromatography (PE/EtOAc=5/1 to 3/1) to give the title compound (1.4 g, 84%). LCMS (M+H).sup.+=230.

Step 3: ethyl 4-bromo-2-(difluoromethyl)-6-methylbenzoate

[0439] ##STR00208##

[0440] Copper bromide (1.37 g, 6.11 mmol) and t-butyl-nitrite (1.57 g, 15.3 mmol) was suspended in CH.sub.3CN (40 mL). The mixture was cooled to 0? C. and ethyl 4-amino-2-(difluoromethyl)-6-methylbenzoate (1.4 g, 6.11 mmol) in CH.sub.3CN (10 mL) was added dropwise. After 1 h, the mixture warmed to room temperature and stirred for 4 h. Water (30 mL) was added and the pH of the solution was adjusted to 2 with aqueous HCl (2 M). The mixture was extracted with EtOAc (20 mL?2). The combined organic layer was washed with brine (30 mL), dried over Na.sub.2SO.sub.4 and filtered. The filtrate was concentrated under reduced pressure and the crude was purified by silica gel chromatography (PE/EtOAc=5/1 to 3/1) to give the title compound (1.1 g, 61%). LCMS (M+H).sup.+=293, 295.

Step 4: 4-bromo-2-(difluoromethyl)-6-methylbenzoic acid

[0441] ##STR00209##

[0442] A mixture of ethyl 4-bromo-2-(difluoromethyl)-6-methylbenzoate (1.1 g, 3.75 mmol) and NaOH (0.6 g, 15 mmol) in dioxane (20 mL) and water (10 mL) was stirred at 80? C. for overnight. The mixture was cooled to room temperature and concentrated. Water (10 mL) was added and the pH of the mixture was adjusted to 2 with aqueous HCl (2 M). The precipitate was collected by filtration and dried under vacuum to give the title compound (0.60 g, 60%).

Step 5: 4-bromo-2-(difluoromethyl)-N-(2-(dimethylamino)ethyl)-6-methylbenzamide

[0443] ##STR00210##

[0444] The title compound (0.64 g, 84%) was prepared in a manner similar to that in Example A1 step 5 from 4-bromo-2-(difluoromethyl)-6-methylbenzoic acid and N1,N1-dimethylethane-1,2-diamine. LCMS (M+H).sup.+=335, 337.

Step 6: 2-(difluoromethyl)-N-(2-(dimethylamino)ethyl)-6-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide

[0445] ##STR00211##

[0446] The title compound (0.40 g, 55%) was prepared in a manner similar to that in Example A1 step 6 from 4-bromo-2-(difluoromethyl)-N-(2-(dimethylamino)ethyl)-6-methylbenzamide and BPD. LC-MS (M+H).sup.+=383.1.

Step 7: 4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2-(difluoromethyl)-N-(2-(dimethylamino)ethyl)-6-methylbenzamide

[0447] Example A33 (140 mg, 62%) was prepared in a manner similar to that in Example A1 step 6 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and 2-(difluoromethyl)-N-(2-(dimethylamino)ethyl)-6-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide. .sup.1H NMR (400 MHz, DMSO-d6) ? 8.44 (t, J=5.7 Hz, 1H), 8.35 (s, 1H), 8.10 (s, 1H), 7.9 (s, 1H) 7.88 (s, 1H) 7.58 (s, 1H), 7.14-6.83 (m, 3H), 4.16-4.06 (m, 1H), 3.38-3.34 (m, 2H), 2.90-2.81 (m, 2H), 2.38 (t, J=6.5 Hz, 2H), 2.31 (s, 3H), 2.20 (s, 3H), 2.19 (s, 6H), 2.08-1.95 (m, 6H). LCMS (M+H).sup.+=529.5.

Example A34

(R)-4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-N-(2-(3-fluoropyrrolidin-1-yl)ethyl)-2,6-dimethylbenzamide

[0448] ##STR00212##

Step 1: (R)-2-(3-fluoropyrrolidin-1-yl)acetonitrile

[0449] ##STR00213##

[0450] (R)-3-fluoropyrrolidine hydrochloride (1.0 g, 7.9 mmol), 2-bromoacetonitrile (0.55 mL, 7.9 mmol) and K.sub.2CO.sub.3 (3.3 g, 23.8 mmol) was suspended in CH.sub.3CN (30 mL) and the mixture was heated to reflux for overnight. The mixture was cooled to room temperature, then partitioned between water (50 mL) and EtOAc (40 mL). The organic layer was dried over Na.sub.2SO.sub.4, filtered and the filtrate was concentrated in vacuo to give the title compound (1.0 g, 99%). LC-MS (M+H).sup.+=129.0.

Step 2: (R)-2-(3-fluoropyrrolidin-1-yl)ethan-1-amine

[0451] ##STR00214##

[0452] To a solution of (R)-2-(3-fluoropyrrolidin-1-yl)acetonitrile (1.0 g, 7.8 mmol) in THF (30 mL) was added LiAlH.sub.4 (740 mg, 19.5 mmol) at 0? C., then the mixture was heated to reflux for overnight. The mixture was cool to room temperature and water (4.0 mL) was added. After 15 min, the mixture filtered and the filter cake was washed with THF (20 mL). The filtrate was dried over Na.sub.2SO.sub.4, filtered and the filtrate was concentrated in vacuo to give the title compound (240 mg, 24%). LC-MS (M+H).sup.+=133.1.

Step 3: (R)-4-bromo-N-(2-(3-fluoropyrrolidin-1-yl)ethyl)-2,6-dimethylbenzamide

[0453] ##STR00215##

[0454] The title compound (433 mg, 70%) was prepared in a manner similar to that in Example A3 step 1 from 4-bromo-2,6-dimethylbenzoic acid and (R)-2-(3-fluoropyrrolidin-1-yl)ethan-1-amine. LC-MS (M+H).sup.+=343.0.

Step 4: (R)N-(2-(3-fluoropyrrolidin-1-yl)ethyl)-2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide

[0455] ##STR00216##

[0456] The title compound (90 mg, 30%) was prepared in a manner similar to that in Example A1 step 6 from (R)-4-bromo-N-(2-(3-fluoropyrrolidin-1-yl)ethyl)-2,6-dimethylbenzamide and BPD. LC-MS (M+H).sup.+=391.2.

Step 5: (R)-4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-N-(2-(3-fluoropyrrolidin-1-yl)ethyl)-2,6-dimethylbenzamide

[0457] Example A34 (10 mg, 7%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and (R)N-(2-(3-fluoropyrrolidin-1-yl)ethyl)-2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide. .sup.1H NMR (400 MHz, DMSO) ? 8.25-8.19 (m, 2H), 8.12 (s, 1H), 7.58 (s, 1H), 7.50 (s, 2H), 6.73 (s, 2H), 5.29-5.08 (m, 1H), 4.15-4.09 (m, 1H), 3.36 (d, J=6.5 Hz, 1H), 2.91-2.78 (m, 5H), 2.70-2.53 (m, 3H), 2.35-2.30 (m, 1H), 2.23 (s, 6H), 2.20 (s, 3H), 2.18-1.77 (m, 9H). LC-MS (M+H).sup.+=537.3.

Example A35

5-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylphenyl)morpholin-3-one

[0458] ##STR00217##

Step 1: 5-(4-bromo-2,6-dimethylphenyl)morpholin-3-one

[0459] ##STR00218##

[0460] To a solution of 2-amino-2-(4-bromo-2,6-dimethylphenyl)ethan-1-ol hydrochloride (200 mg, 0.71 mmol) and triethylamine (203 mg, 1.91 mmol) in THF (15 mL) was added chloroacetyl chloride (91 mg, 0.76 mmol) dropwise at 0? C. under nitrogen. After 15 min, water (10 mL) was added. The mixture was extracted with EtOAc (10 mL?3). The combined organic layer was concentrated under reduced pressure. The residue was dissolved in THF (15 mL), and NaH (60%, 37 mg, 0.92 mmol) was added in portions at 0? C. The mixture was warmed to room temperature and stirred for 1.5 h. Saturated NH.sub.4Cl (50 mL) was added and the mixture was extracted with EtOAc (50 mL?3). The combined organic layer was washed with brine (50 mL), dried over Na.sub.2SO.sub.4 and filtered. The filtrate was concentrated under reduced pressure and the residue was purified by silica gel chromatography (MeOH/DCM=1:12) to give the title compound (123 mg, 61%). LC-MS (M+H).sup.+=284.0.

Step 2: 5-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)morpholin-3-one

[0461] ##STR00219##

[0462] The title compound (123 mg, 96%) was prepared in a manner similar to that in Example A1 step 6 from 5-(4-bromo-2,6-dimethylphenyl)morpholin-3-one and BPD. LC-MS (M+H).sup.+=332.3.

Step 3: 5-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylphenyl)morpholin-3-one

[0463] Example A35 (16 mg, 16%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and 5-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)morpholin-3-one. .sup.1H NMR (300 MHz, DMSO-d.sub.6) ? 8.32 (s, 1H), 8.21 (s, 1H), 8.10 (s, 1H), 7.56 (s, 1H), 7.47 (s, 2H), 6.71 (s, 2H), 5.13-5.03 (m, 1H), 4.18-4.10 (m, 3H), 3.95-3.84 (m, 1H), 3.72-3.59 (m, 1H), 2.90-2.79 (m, 2H), 2.37 (s, 6H), 2.20 (s, 3H), 2.13-1.93 (m, 6H). LC-MS (M+H).sup.+=478.2.

Example A36

1-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylbenzyl)-3-ethylurea

[0464] ##STR00220##

Step 1: 1-(4-bromo-2,6-dimethylbenzyl)-3-ethylurea

[0465] ##STR00221##

[0466] To a stirred solution of 1-(4-bromo-2,6-dimethylphenyl)methanamine (150 mg, 0.70 mmol) and triethylamine (142 mg, 1.40 mmol) in DCM (5 mL) was added ethyl isocyanate (50 mg, 0.70 mmol) in DCM (5 mL) dropwise at 0? C. The mixture was warmed to room temperature and stirred for 3 h. The mixture was partitioned between water (10 mL) and DCM (10 mL). The organic layer was separated, dried over anhydrous Na.sub.2SO.sub.4 and filtered. The filtrate was concentrated under reduced pressure to give the title compound (144 mg, 72%). LC-MS (M+H).sup.+=287.1.

Step 2: 1-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)-3-ethylurea

[0467] ##STR00222##

[0468] The title compound (82 mg, 59%) was prepared in a manner similar to that in Example A1 step 6 from 1-(4-bromo-2,6-dimethylbenzyl)-3-ethylurea and BPD. LC-MS (M+H).sup.+=333.1.

Step 3: 1-[[4-(5-amino-6-[[1-(1-methylpiperidin-4-yl)pyrazol-4-yl]oxy]pyrazin-2-yl)-2,6-dimethylphenyl]methyl]-3-ethylurea

[0469] Example A36 (18 mg, 19%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and 1-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)-3-ethylurea. .sup.1H NMR (300 MHz, DMSO-d6) ? 8.19 (s, 1H), 8.10 (s, 1H), 7.57 (s, 1H), 7.46 (s, 2H), 6.67 (s, 2H), 5.86-5.78 (m, 1H), 5.65-5.57 (m, 1H), 4.21-4.12 (m, 1H), 4.19-4.04 (m, 2H), 3.05-2.93 (m, 2H), 2.90-2.80 (m, 2H), 2.32 (s, 6H), 2.20 (s, 3H), 2.14-1.88 (m, 6H), 0.95 (t, J=7.1 Hz, 3H). LC-MS (M+H).sup.+=479.4.

Example A37

1-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylbenzyl)-3-cyclopentylurea

[0470] ##STR00223##

Step 1: 1-(4-bromo-2,6-dimethylbenzyl)-3-cyclopentylurea

[0471] ##STR00224##

[0472] The title compound (68 mg, 45%) was prepared in a manner similar to that in Example A26 step 1 from 1-(4-bromo-2,6-dimethylphenyl)methanamine and cyclopentylamine. LC-MS (M?H).sup.+=323.1.

Step 2: 1-cyclopentyl-3-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)urea

[0473] ##STR00225##

[0474] The title compound (33 mg, 53%) was prepared in a manner similar to that in Example A1 step 6 from 1-(4-bromo-2,6-dimethylbenzyl)-3-cyclopentylurea and BPD. LC-MS (M+H).sup.+=373.2.

Step 3: 1-(4-(5-amino-64(1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylbenzyl)-3-cyclopentylurea

[0475] Example A37 (9 mg, 8%) was prepared in a manner similar to that in Example A1 final step from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and 1-cyclopentyl-3-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)urea. .sup.1H NMR (300 MHz, DMSO-d6) ? 8.19 (s, 1H), 8.10 (s, 1H), 7.57 (s, 1H), 7.46 (s, 2H), 6.66 (s, 2H), 5.75-5.64 (m, 2H), 4.25-4.05 (m, 3H), 3.89-3.81 (m, 1H), 2.88-2.79 (m, 2H), 2.32 (s, 6H), 2.19 (s, 3H), 2.12-1.90 (m, 6H), 1.80-1.66 (m, 2H), 1.60-1.39 (m, 4H), 1.30-1.14 (m, 3H). LC-MS (M+H).sup.+=519.4.

Example A38

N-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylbenzyl)benzenesulfonamide

[0476] ##STR00226##

Step 1: N-(4-bromo-2,6-dimethylbenzyl)benzenesulfonamide

[0477] ##STR00227##

[0478] The title compound (116 mg, 23%) was prepared in a manner similar to that in Example A20 step 5 from 1-(4-bromo-2,6-dimethylphenyl)methanamine and benzenesulfonyl chloride. LC-MS (M?H).sup.?=352.0.

Step 2: N-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)benzenesulfonamide

[0479] ##STR00228##

[0480] The title compound (190 mg, 64%) was prepared in a manner similar to that in Example A1 step 6 from N-(4-bromo-2,6-dimethylbenzyl)benzenesulfonamide and BPD. LC-MS (M?H).sup.?=400.1.

Step 3: N-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylbenzyl)benzenesulfonamide

[0481] Example A38 (24 mg, 10%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and N-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)benzenesulfonamide. .sup.1H NMR (400 MHz, DMSO-d6) ? 8.21 (s, 1H), 8.10 (s, 1H), 7.91-7.84 (m, 2H), 7.72-7.59 (m, 4H), 7.58 (s, 1H), 7.45 (s, 2H), 6.70 (s, 2H), 4.19-4.07 (m, 1H), 3.92-3.84 (m, 2H), 2.92-2.82 (m, 2H), 2.21 (d, J=13.2 Hz, 9H), 2.15-1.93 (m, 6H). LC-MS (M+H).sup.+=548.4.

Example A39

N-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylbenzyl)-4-methoxybenzenesulfonamide

[0482] ##STR00229##

Step 1: N-(4-bromo-2,6-dimethylbenzyl)-4-methoxybenzenesulfonamide

[0483] ##STR00230##

[0484] The title compound (107 mg, 20%) was prepared in a manner similar to that in Example A20 step 5 from 1-(4-bromo-2,6-dimethylphenyl)methanamine and 4-methoxybenzenesulfonyl chloride. LC-MS (M?H).sup.?=382.0.

Step 2: N-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)-4-methoxybenzenesulfonamide

[0485] ##STR00231##

[0486] The title compound (118 mg, 98%) was prepared in a manner similar to that in Example A1 step 6 from N-(4-bromo-2,6-dimethylbenzyl)-4-methoxybenzenesulfonamide and BPD. LC-MS (M+H).sup.+=432.3.

Step 3: N-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylbenzyl)-4-methoxybenzenesulfonamide

[0487] Example A39 (26 mg, 18%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and N-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)-4-methoxybenzenesulfonamide. .sup.1H NMR (400 MHz, DMSO-d6) ? 8.21 (s, 1H), 8.10 (s, 1H), 7.84-7.76 (m, 2H), 7.58 (s, 1H), 7.51-7.47 (m, 1H), 7.45 (s, 2H), 7.18-7.10 (m, 2H), 6.70 (s, 2H), 4.22-4.07 (m, 1H), 3.87-3.81 (m, 5H), 2.95-2.85 (m, 2H), 2.26 (s, 3H), 2.21 (s, 6H), 2.14 (s, 3H), 2.17-1.97 (m, 6H). LC-MS (M+H).sup.+=578.4.

Example A40

N-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylbenzyl)cyclopentanesulfonamide

[0488] ##STR00232##

Step 1: N-(4-bromo-2,6-dimethylbenzyl)cyclopentanesulfonamide

[0489] ##STR00233##

[0490] The title compound (71 mg, 23%) was prepared in a manner similar to that in Example A20 step 5 from 1-(4-bromo-2,6-dimethylphenyl)methanamine and cyclopentanesulfonyl chloride. LC-MS (M?H).sup.+=344.0.

Step 2: N-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)cyclopentanesulfonamide

[0491] ##STR00234##

The title compound (78 mg, 96%) was prepared in a manner similar to that in Example A1 step 6 from N-(4-bromo-2,6-dimethylbenzyl)cyclopentanesulfonamide and BPD. LC-MS (M?H)?=392.2.

Step 3: N-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylbenzyl)cyclopentanesulfonamide

[0492] Example A40 (19 mg, 13%) was prepared in a manner similar to that in Example A1 final step from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and N-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)cyclopentanesulfonamide. .sup.1H NMR (300 MHz, DMSO-d6) ? 8.22 (s, 1H), 8.10 (s, 1H), 7.57 (s, 1H), 7.48 (s, 2H), 7.12-7.03 (m, 1H), 6.69 (s, 2H), 4.19-4.05 (m, 3H), 3.65-3.52 (m, 1H), 2.91-2.81 (m, 2H), 2.36 (s, 6H), 2.21 (s, 3H), 2.15-1.83 (m, 10H), 1.73-1.47 (m, 4H). LC-MS (M+H).sup.+=540.4.

Example A41

3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-N-methyl-5-(piperidin-1-yl)benzenesulfonamide

[0493] ##STR00235##

Step 1: 3-bromo-5-fluoro-N-methylbenzenesulfonamide

[0494] ##STR00236##

[0495] The title compound (1.62 g, 91%) was prepared in a manner similar to that in Example A8 step 3 from 3-bromo-5-fluorobenzenesulfonyl chloride. LC-MS (M+H).sup.+=267.8.

Step 2: 3-bromo-N-methyl-5-(piperidin-1-yl)benzenesulfonamide

[0496] ##STR00237##

[0497] A mixture of 3-bromo-5-fluoro-N-methylbenzenesulfonamide (255 mg, 0.951 mmol), piperidine (476 mg, 5.6 mmol) and K.sub.2CO.sub.3 (309 mg, 2.24 mmol) in DMF (3 mL) was stirred for 16 h at 120? C. under nitrogen. The mixture was cooled to room temperature and concentrated under reduced pressure. The residue was purified by C18 chromatography to give the title compound (274 mg, 86%). LC-MS (M+H).sup.+=334.9.

Step 3: N-methyl-3-(piperidin-1-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide

[0498] ##STR00238##

[0499] The title compound (257 mg, 82%) was prepared in a manner similar to that in Example A1 step 6 from 3-bromo-N-methyl-5-(piperidin-1-yl)benzenesulfonamide and BPD. LC-MS (M?pin).sup.+=299.1.

Step 4: 3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-N-methyl-5-(piperidin-1-yl)benzenesulfonamide

[0500] Example A41 (25 mg, 18%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and N-methyl-3-(piperidin-1-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide. .sup.1H NMR (400 MHz, DMSO-d6) ? 8.31 (s, 1H), 8.10 (s, 1H), 7.62-7.54 (m, 3H), 7.38-7.31 (m, 1H), 7.17-7.14 (m, 1H), 6.86 (s, 2H), 4.15-4.02 (m, 1H), 3.28-3.20 (m, 4H), 2.91-2.82 (m, 2H), 2.41 (d, J=5.1 Hz, 3H), 2.21 (s, 3H), 2.10-1.89 (m, 6H), 1.67-1.55 (m, 6H). LC-MS (M+H).sup.+=527.3.

Example A42

3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-N-methyl-5-morpholinobenzenesulfonamide

[0501] ##STR00239##

Step 1: 3-bromo-N-methyl-5-morpholinobenzenesulfonamide

[0502] ##STR00240##

[0503] The title compound (279 mg, 88%) was prepared in a manner similar to that in Example A41 step 2 from 3-bromo-5-fluoro-N-methylbenzenesulfonamide and morpholine. LC-MS (M+H).sup.+=334.8.

Step 2: N-methyl-3-morpholino-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide

[0504] ##STR00241##

[0505] The title compound (144 mg, 66%) was prepared in a manner similar to that in Example A1 step 6 from 3-bromo-N-methyl-5-(morpholin-4-yl)benzenesulfonamide and BPD. LC-MS (M+H).sup.+=383.0.

Step 3: 3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-N-methyl-5-morpholinobenzenesulfonamide

[0506] Example A42 (28 mg, 21%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and N-methyl-3-morpholino-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide. .sup.1H NMR (400 MHz, DMSO-d6) ? 8.34 (s, 1H), 8.11 (s, 1H), 7.65 (s, 1H), 7.63-7.56 (m, 2H), 7.40-7.34 (m, 1H), 7.18 (s, 1H), 6.88 (s, 2H), 4.15-4.04 (m, 1H), 3.81-3.72 (m, 4H), 3.27-3.18 (m, 4H), 2.91-2.83 (m, 2H), 2.42 (d, J=5.1 Hz, 3H), 2.21 (s, 3H), 2.11-1.88 (m, 6H). LC-MS (M+H).sup.+=529.3.

Example A43

(R)-3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-N-methyl-5-(2-methylpyrrolidin-1-yl)benzenesulfonamide

[0507] ##STR00242##

Step 1: (R)-3-bromo-N-methyl-5-(2-methylpyrrolidin-1-yl)benzenesulfonamide

[0508] ##STR00243##

[0509] The title compound (286 mg, 90%) was prepared in a manner similar to that in Example A41 step 2 from 3-bromo-5-fluoro-N-methylbenzenesulfonamide and (2R)-2-methylpyrrolidine. LC-MS (M+H).sup.+=332.8.

Step 2: (R)N-methyl-3-(2-methylpyrrolidin-1-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide

[0510] ##STR00244##

[0511] The title compound (202 mg, 74%) was prepared in a manner similar to that in Example A1 step 6 from (R)-3-bromo-N-methyl-5-(2-methylpyrrolidin-1-yl)benzenesulfonamide and BPD. LC-MS (M?pin).sup.+=299.1.

Step 3: (R)-3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-N-methyl-5-(2-methylpyrrolidin-1-yl)benzenesulfonamide

[0512] Example A43 (39 mg, 30%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and (R)N-methyl-3-(2-methylpyrrolidin-1-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide. .sup.1H NMR (400 MHz, DMSO-d6) ? 8.25 (s, 1H), 8.08 (s, 1H), 7.60 (s, 1H), 7.41 (s, 1H), 7.38-7.30 (m, 1H), 7.19 (s, 1H), 6.89-6.75 (m, 3H), 4.15-4.01 (m, 1H), 3.97-3.90 (m, 1H), 3.49-3.38 (m, 1H), 3.23-3.11 (m, 1H), 2.93-2.81 (m, 2H), 2.42 (d, J=5.1 Hz, 3H), 2.22 (s, 3H), 2.12-1.90 (m, 9H), 1.74-1.67 (m, 1H), 1.16-1.08 (m, 3H). LC-MS (M+H).sup.+=527.3.

Example A44

N-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylbenzyl)benzamide

[0513] ##STR00245##

Step 1: N-(4-bromo-2,6-dimethylbenzyl)benzamide

[0514] ##STR00246##

[0515] To a stirred mixture of 1-(4-bromo-2,6-dimethylphenyl)methanamine (150 mg, 0.70 mmol) and benzoyl chloride (394 mg, 2.80 mmol) in DCM (5 mL) was added triethylamine (213 mg, 2.10 mmol) dropwise at 0? C. under nitrogen. The mixture was warmed for room temperature and stirred for 2 h. The mixture was concentrated under reduced pressure. The residue was purified by silica gel chromatography (PE/EtOAc=8:1) to give the title compound (200 mg, 89%). LC-MS (M+H).sup.+=318.1.

Step 2: N-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)benzamide

[0516] ##STR00247##

[0517] The title compound (146 mg, 66%) was prepared in a manner similar to that in Example A1 step 6 from N-(4-bromo-2,6-dimethylbenzyl)benzamide and BPD. LC-MS (M+H).sup.+=366.1.

Step 3: N-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylbenzyl)benzamide

[0518] Example A44 (7 mg, 3%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and N-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)benzamide. .sup.1H NMR (400 MHz, DMSO-d6) ? 8.51-8.44 (m, 1H), 8.23 (s, 1H), 8.12 (s, 1H), 7.88-7.80 (m, 2H), 7.59 (s, 1H), 7.54-7.46 (m, 3H), 7.46-7.39 (m, 2H), 6.69 (s, 2H), 4.53-4.43 (m, 2H), 4.19-4.07 (m, 1H), 2.90-2.78 (m, 2H), 2.39 (app s, 6H), 2.20 (s, 3H), 2.12-1.90 (m, 6H). LC-MS (M+H).sup.+=512.4.

Example A45

N-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylbenzyl)acetamide

[0519] ##STR00248##

Step 1: N-(4-bromo-2,6-dimethylbenzyl)acetamide

[0520] ##STR00249##

[0521] The title compound (131 mg, 84%) was prepared in a manner similar to that in Example A44 step 1 from 1-(4-bromo-2,6-dimethylphenyl)methanamine and AcCl. LC-MS (M+H).sup.+=256.0.

Step 2: N-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)acetamide

[0522] ##STR00250##

[0523] The title compound (88 mg, 80%) was prepared in a manner similar to that in Example A1 step 6 from N-(4-bromo-2,6-dimethylbenzyl)benzamide and BPD. LC-MS (M+H).sup.+=304.3.

Step 3: N-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylbenzyl)acetamide

[0524] Example A45 (19 mg, 13%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and N-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)acetamide. .sup.1H NMR (300 MHz, DMSO-d6) ? 8.20 (s, 1H), 8.10 (s, 1H), 7.87-7.80 (m, 2H), 7.57 (s, 1H), 7.50-7.45 (m, 2H), 6.68 (s, 2H), 4.28-4.20 (m, 2H), 4.19-4.07 (m, 1H), 2.91-2.80 (m, 2H), 2.35-2.29 (m, 6H), 2.20 (s, 3H), 2.13-1.90 (m, 6H), 1.79 (s, 3H). LC-MS (M+H).sup.+=450.4.

Example A46

N-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2-methylbenzyl)methanesulfonamide

[0525] ##STR00251##

Step 1: (4-bromo-2-methylphenyl)methanamine

[0526] ##STR00252##

[0527] The title compound (2.29 g, 47%) was prepared in a manner similar to that in Example A19 step 1 from 4-bromo-2-methylbenzonitrile. LC-MS (M+H).sup.+=200.0.

Step 2: N-(4-bromo-2-methylbenzyl)methanesulfonamide

[0528] ##STR00253##

[0529] The title compound (377 mg, 59%) was prepared in a manner similar to that in Example A20 step 5 from (4-bromo-2-methylphenyl)methanamine and MsCl. LC-MS (M+H).sup.+=277.7.

Step 2: N-(2-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)methanesulfonamide

[0530] ##STR00254##

[0531] The title compound (142 mg, 71%) was prepared in a manner similar to that in Example A1 step 6 from N-(4-bromo-2-methylbenzyl)methanesulfonamide and BPD. LC-MS (M+H).sup.+=326.2.

Step 3: N-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2-methylbenzyl)methanesulfonamide

[0532] Example A46 (24 mg, 21%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and N-(2-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)methanesulfonamide. .sup.1H NMR (400 MHz, DMSO-6) ? 8.24 (s, 1H), 8.09 (s, 1H), 7.70-7.58 (m, 3H), 7.39 (t, J=6.0 Hz, 1H), 7.33 (d, J=7.6 Hz, 1H), 6.70 (s, 2H), 4.22-4.06 (m, 3H), 2.95-2.81 (m, 5H), 2.33 (s, 3H), 2.21 (s, 3H), 2.11-1.92 (m, 6H). LC-MS (M+H).sup.+=472.3.

Example A47

1-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2-methylbenzyl)-3-methylurea

[0533] ##STR00255##

Step 1: 1-(4-bromo-2-methylbenzyl)-3-methylurea

[0534] ##STR00256##

[0535] To a stirred mixture of 1-(4-bromo-2-methylphenyl)methanamine (460 mg, 2.292 mmol) and N-methylcarbamoyl chloride (338 mg, 3.43 mmol) in DCM (5 mL) was added triethylamine (473 mg, 4.58 mmol) at room temperature under nitrogen. After 3 h, the mixture was poured into water (50 mL) and extracted with DCM (50 mL?3). The combined organic layer was washed with brine (50 mL), dried over anhydrous Na.sub.2SO.sub.4 and filtered. The filtrate was concentrated under reduced pressure to give the title compound (550 mg, 93%). LC-MS (M+H).sup.+=259.0.

Step 2: 1-methyl-3-(2-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)urea

[0536] ##STR00257##

[0537] The title compound (140 mg, 68%) was prepared in a manner similar to that in Example A1 step 6 from 1-(4-bromo-2-methylbenzyl)-3-methylurea and BPD. LC-MS (M+H).sup.+=305.0.

Step 3: 1-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2-methylbenzyl)-3-methylurea

[0538] Example A47 (13 mg, 12%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and 1-methyl-3-(2-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)urea .sup.1H NMR (400 MHz, DMSO-d6) ? 8.21 (s, 1H), 8.09 (s, 1H), 7.66-7.58 (m, 3H), 7.20 (d, J=8.0 Hz, 2H), 6.67 (s, 2H), 6.24 (t, J=5.6 Hz, 1H), 5.77 (q, J=4.8 Hz, 1H), 4.22-4.08 (m, 3H), 2.94-2.83 (m, 2H), 2.57 (d, J=4.4 Hz, 3H), 2.28 (s, 3H), 2.22 (s, 3H), 2.15-1.90 (m, 6H). LC-MS (M+H).sup.+=451.4.

Example A48

5-(3,5-dimethyl-4-(((2,2,2-trifluoroethyl)amino)methyl)phenyl)-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine

[0539] ##STR00258##

Step 1: 4-bromo-2,6-dimethyl-N-(2,2,2-trifluoroethyl)benzamide

[0540] ##STR00259##

[0541] 4-bromo-2,6-dimethylbenzoic acid (1.5 g, 6.55 mmol) and DMF (2 drops) was dissolved in DCM (20 mL). Oxalyl chloride (1.1 mL, 13.1 mmol) was added dropwise at 0? C. and the mixture was warmed to room temperature then stirred for 1 h. The mixture was concentrated under vacuum. The crude was dissolved in anhydrous THF (10 mL) then the solution was added dropwise to a mixture of 2,2,2-trifluoroethan-1-amine (714 mg, 7.20 mmol) and DIPEA (2.55 mL, 14.41 mmol) in anhydrous THF (20 mL) at 0? C. The mixture was warmed to room temperature then stirred for 2 h. Water (100 mL) was carefully added, and the mixture was extracted with EtOAc (50 mL?3). The combined organic laver was washed with brine (50 mL), dried over Na.sub.2SO.sub.4 then concentrated under vacuum. The residue was purified by silica gel chromatography to give the title compound (1.8 g, 89%). LC-MS (M+H).sup.+=311.0.

Step 2: N-(4-bromo-2,6-dimethylbenzyl)-2,2,2-trifluoroethan-1-amine

[0542] ##STR00260##

[0543] To 4-bromo-2,6-dimethyl-N-(2,2,2-trifluoroethyl)benzamide (1.7 g, 5.48 mmol) was added BH.sub.3-THF complex (1.0 M, 22 mL, 22 mmol) and the mixture was heated to reflux for 24 h. The mixture was cooled to 0? C. and MeOH (10 mL) was added. The mixture was concentrated under reduced pressure. The residue was purified by silica gel chromatography to give the title compound (600 mg, 37%). LC-MS (M+H).sup.+=297.0.

Step 3: 5-(3,5-dimethyl-4-(((2,2,2-trifluoroethyl)amino)methyl)phenyl)-34(1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine

[0544] A solution of N-(4-bromo-2,6-dimethylbenzyl)-2,2,2-trifluoroethan-1-amine (200 mg, 0.675 mmol), BPD (257 mg, 1.01 mmol), KOAc (133 mg, 1.35 mmol) and Pd(dppl)Cl.sub.2 (25 mg, 0.034 mmol) in 1,4-dioxane (20 mL) was heated to reflux under N.sub.2 for 2 h. The solution was cooled to room temperature, then 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine (239 mg, 0.675 mmol), K.sub.2CO.sub.3 (186 mg, 1.35 mmol), Pd(dppf)Cl.sub.2 (25 mg, 0.034 mmol) and water (10 mL) was added. The mixture was heated to reflux under N.sub.2 for 12 h then cooled to room temperature. The solvent was concentrated under reduced pressure to give Example A48 (80 mg, 24%). .sup.1H NMR (400 MHz, DMSO-d6) ? 8.21 (s, 1H), 8.12 (s, 1H), 7.58 (s, 1H), 7.47 (s, 2H), 6.67 (s, 2H), 4.14-4.10 (m, 1H), 3.75 (d, J=6.5 Hz, 2H), 3.31-3.27 (m, 2H), 2.86 (d, J=11.2 Hz, 2H), 2.36 (s, 6H), 2.21 (s, 3H), 2.11-1.96 (m, 6H). LC-MS (M+H).sup.+=490.0.

Example A49

(R)-3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-N-methyl-5-(3-methylmorpholino)benzenesulfonamide

[0545] ##STR00261##

Step 1: 3-bromo-5-chloro-N-methylbenzenesulfonamide

[0546] ##STR00262##

[0547] The title compound (596 mg, 61%) was prepared in a manner similar to that in Example A7 step 1 from 3-bromo-5-chlorobenzenesulfonyl chloride.

Step 2: (R)-3-chloro-N-methyl-5-(3-methylmorpholino)benzenesulfonamide

[0548] ##STR00263##

[0549] To a stirred mixture of 3-bromo-5-chloro-N-methylbenzenesulfonamide (560 mg, 1.95 mmol) and (3R)-3-methylmorpholine (395 mg, 3.91 mmol) in dioxane (10 mL) was added Pd(dba).sub.2 (112 mg, 0.20 mmol), JohnPhos (58 mg, 0.20 mmol) and t-BuOK (43.9 mg, 0.39 mmol) at room temperature under nitrogen. The mixture was stirred for 2 h at 100? C. The mixture was cooled to room temperature and concentrated under vacuum. The residue was purified by C.sub.18 flash chromatography to give the title compound (268 mg, 45%). LC-MS (M+H).sup.+=305.0.

Step 3: (R)N-methyl-3-(3-methylmorpholino)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide

[0550] ##STR00264##

[0551] The title compound (248 mg, 83%) was prepared in a manner similar to that in Example A1 step 6 from (R)-3-chloro-N-methyl-5-(3-methylmorpholino)benzenesulfonamide and BPD. LC-MS (M?pin).sup.+=315.1.

Step 4: (R)-3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-N-methyl-5-(3-methylmorpholino)benzenesulfonamide

[0552] Example A49 (32 mg, 21%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and (R)N-methyl-3-(3-methylmorpholino)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide. .sup.1H NMR (400 MHz, DMSO-d.sub.6) ? 8.32 (s, 1H), 8.10 (s, 1H), 7.61-7.57 (m, 2H), 7.53 (m, 1H), 7.40-7.34 (m, 1H), 7.12 (s, 1H), 6.88 (s, 2H), 4.17-4.04 (m, 1H), 4.03-3.91 (m, 2H), 3.77-3.67 (m, 2H), 3.62-3.51 (m, 1H), 3.14-3.04 (m, 1H), 2.94-2.84 (m, 2H), 2.41 (d, J=5.2 Hz, 3H), 2.23 (s, 3H), 2.13-1.89 (m, 6H), 1.04 (d, J=6.5 Hz, 3H). LC-MS (M+H).sup.+=543.3.

Example A50

(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylphenyl)dimethylsilanol

[0553] ##STR00265##

Step 1: (3-bromo-5-methylphenyl)(chloromethyl)dimethylsilane

[0554] ##STR00266##

[0555] To a solution of 1,3-dibromo-5-methylbenzene (2.0 g, 8.0 mmol) in THF (20 mL) was added n-BuLi (2.5 M in hexane, 3.2 mL, 8.0 mmol) at ?78? C. under nitrogen. After 1 h, chloro(chloromethyl)dimethylsilane (1.7 g, 12 mmol) was added. After 3 h, the mixture was warmed to room temperature, poured into water (60 mL). The mixture was extracted with EtOAc (60 mL?2). The combined organic layer was washed with brine (50 mL), dried over Na.sub.2SO.sub.4, filtered and concentrated under vacuum. The crude was purified by silica gel column chromatography (PE:EtOAc=5:1) to give the title compound (2.0 g, 90%). .sup.1H NMR (400 MHz, CDCl.sub.3) ? 7.20 (s, 1H), 7.14 (s, 1H), 7.01 (s, 1H), 2.71 (s, 2H), 2.11 (s, 3H), 0.18 (s, 6H).

Step 2: ((3-bromo-5-methylphenyl)dimethylsilyl)methyl acetate

[0556] ##STR00267##

[0557] A mixture of (3-bromo-5-methylphenyl)(chloromethyl)dimethylsilane (2.0 g, 7.2 mmol) and KOAc (2.8 g, 28.8 mmol) in DMF (30 mL) was stirred for 3 h at 90? C. The mixture was cooled to room temperature then diluted with water (60 mL). The mixture was extracted with EtOAc (60 mL?2). The combined organic laver was washed with brine (50 mL), dried over Na.sub.2SO.sub.4, filtered and concentrated under vacuum. The crude was purified by silica gel column chromatography (PE:EtOAc=5:1) to give the title compound (1.6 g, 74%). .sup.1H NMR (400 MHz, CDCl.sub.3) ? 7.40 (s, 1H), 7.33 (s, 1H), 7.20 (s, 1H), 3.91 (s, 2H), 2.31 (s, 3H), 2.02 (s, 3H), 0.32 (s, 6H).

Step 3: ((3-bromo-5-methylphenyl)dimethylsilyl)methanol

[0558] ##STR00268##

[0559] A solution of ((3-bromo-5-methylphenyl)dimethylsilyl)methyl acetate (1.6 g, 5.31 mmol) and K.sub.2CO.sub.3 (1.46 g, 10.6 mmol) in MeOH (30 mL) was stirred for 4 h at room temperature then diluted with water (50 mL). The mixture was extracted with EtOAc (50 mL?2). The combined organic layer was washed with brine (50 mL), dried over Na.sub.2SO.sub.4, filtered and concentrated under vacuum. The crude was purified by silica gel column chromatography (PE:EtOAc=3:1) to give the title compound (1.2 g, 87%). .sup.1H NMR (400 MHz, CDCl.sub.3) ? 7.45 (s, 1H), 7.35 (s, 1H), 7.26 (s, 1H), 3.57 (s, 2H), 2.33 (s, 3H), 0.34 (s, 6H).

Step 4: (3-bromo-5-methylphenyl)dimethylsilanol

[0560] ##STR00269##

[0561] 10% sodium hypochlorite (6.8 g, 9.1 mmol) was slowly added to an aqueous NaHCO.sub.3 solution (0.50 M, 37 mL), then the solution was slowly added to a solution of ((3-bromo-5-methylphenyl)dimethylsilyl)methanol (1.2 g, 4.63 mmol), TEMPO (72 mg, 0.463 mmol), and KBr (55 mg, 0.463 mmol) in acetone (60 mL) at 0? C. The mixture was warmed to room temperature and stirred for 2 h. Then, saturated NH.sub.4Cl (30 mL) was added, and the mixture was extracted with EtOAc (50 mL?3). The combined organic layer was washed with brine (50 mL), dried over Na.sub.2SO.sub.4, filtered and concentrated under vacuum. The crude was purified by silica gel column chromatography (PE:EtOAc=3:1) to give the title compound (0.80 g, 70%). .sup.1H NMR (400 MHz, CDCl.sub.3) ? 7.48 (s, 1H), 7.36 (s, 1H), 7.29 (s, 1H), 2.33 (s, 3H), 0.39 (s, 6H).

Step 5: dimethyl(3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)silanol

[0562] ##STR00270##

[0563] The title compound (500 mg, 70%) was prepared in a manner similar to that in Example A1 step 6 from (3-bromo-5-methylphenyl)dimethylsilanol and BPD. .sup.1H NMR (400 MHz, CDCl.sub.3) ? 7.84 (s, 1H), 7.67 (s, 1H), 7.52 (s, 1H), 2.37 (s, 3H), 1.35 (s, 12H), 0.41 (s, 6H). LCMS (M+H).sup.+=293.1.

Step 6: (3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylphenyl)dimethylsilanol

[0564] Example A50 (30 mg, 16%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and dimethyl(3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)silanol. .sup.1H NMR (400 MHz, DMSO-d6) ? 8.23 (s, 1H), 8.14 (s, 1H), 7.82 (s, 1H), 7.65 (s, 1H), 7.59 (s, 1H), 7.27 (s, 1H), 6.71 (s, 2H), 6.03 (s, 1H), 4.25-4.08 (m, 1H), 2.96-2.86 (m, 2H), 2.33 (s, 3H), 2.26 (s, 3H), 2.16-1.97 (m, 6H), 0.25 (s, 6H). LCMS (M+H).sup.+=439.3.

Example A51

1-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylbenzyl)-3-(2,2,2-trifluoroethyl)urea

[0565] ##STR00271##

Step 1: tert-butyl (4-bromo-2,6-dimethylbenzyl)carbamate

[0566] ##STR00272##

[0567] To a solution of (4-bromo-2,6-dimethylphenyl)methanamine (300 mg, 1.4 mmol) in THF (10 mL) was added triethylamine (283 mg, 2.8 mmol), (Boc).sub.2O (448 mg, 2.8 mmol) then the mixture was stirred for overnight at room temperature. EtOAc (10 mL) was added and the mixture was successively washed with H.sub.2O (5 mL) and brine (5 mL), dried over Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by silica gel column (PE:EtOAc=20:1) to give the title compound (380 mg, 86%). LC-MS (M+H).sup.+=314.2, 316.2.

Step 2: tert-butyl (2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)carbamate

[0568] ##STR00273##

[0569] The title compound (250 mg, 69%) was prepared in a manner similar to that in Example A1 step 6 from tert-butyl (4-bromo-2,6-dimethylbenzyl)carbamate and BPD. LC-MS (M+H).sup.+=362.3.

Step 3: tert-butyl (4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylbenzyl)carbamate

[0570] ##STR00274##

[0571] 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine (188 mg, 0.5 mmol), tert-butyl (2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)carbamate (250 mg, 0.7 mmol), Pd(dppf)Cl.sub.2CH.sub.2Cl.sub.2 (43 mg, 0.05 mmol) and K.sub.2CO.sub.3 (219 mg, 1.6 mmol) was added in dioxane (10 mL) and H.sub.2O (1 mL) under nitrogen and the mixture was heated to reflux for overnight. The mixture was cooled to room temperature and EtOAc (15 mL) was added. The mixture was washed with brine (10 mL?2), and the aqueous layer was back extracted with EtOAc (15 mL). The combined organic layer was dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure. The crude was purified by prep-TLC (DCM:MeOH=15:1) to give the title compound (180 mg, 67%). LC-MS (M+H).sup.+=508.6.

Step 4: 5-(4-(aminomethyl)-3,5-dimethylphenyl)-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine; bis-trifluoroacetic acid

[0572] ##STR00275##

[0573] To a solution of tert-butyl (4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylbenzyl)carbamate (180 mg, 0.36 mmol) in DCM (4 mL) was added TFA (2 mL) dropwise at 0? C. The mixture was stirred for 1 h at room temperature and then concentrated under vacuum to give the title compound (225 mg, 100%). LC-MS (M+H).sup.+=408.5.

Step 5: 1-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylbenzyl)-3-(2,2,2-trifluoroethyl)urea

[0574] A mixture of 2,2,2-trifluoroethan-1-amine (121 mg, 1.2 mmol) and pyridine (240 mg, 3.1 mmol) in DCM (5 mL) was cooled to 0? C. and a solution of triphosgene (134 mg, 0.45 mmol) in DCM (5 mL) was added dropwise. The reaction mixture was warmed to 35? C. and stirred for 1 h and then 25? C. for 2 h. An aliquot (1.0 mL) of the mixture was added to a solution of 5-(4-(aminomethyl)-3,5-dimethylphenyl)-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine; bis-trifluoroacetic acid (20 mg, 0.031 mmol) and triethylamine (15 mg, 0.15 mmol) in DCM (1.0 mL) at 0? C. After 3 h, DCM (10 mL) was added and the mixture was successively washed with H.sub.2O (5 mL) and brine (5 mL), dried over Na.sub.2SO.sub.4, filtered and concentrated under vacuum. The residue was purified by prep-HPLC to give Example A51 (2.8 mg, 17%). .sup.1H NMR (400 MHz, DMSO-d6) ? 8.22 (s, 1H), 8.12 (s, 1H), 7.58 (s, 1H), 7.49 (s, 2H), 6.70 (s, 2H), 6.26 (s, 2H), 4.24 (s, 2H), 4.16-4.10 (m, 1H), 3.86-3.79 (m, 2H), 2.86-2.81 (m, 2H), 2.34 (s, 6H), 2.21 (s, 3H), 2.03-1.92 (m, 6H). LC-MS (M+H).sup.+=533.4.

Example A52

2-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylphenyl)propan-2-ol

[0575] ##STR00276##

Step 1: methyl 3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate

[0576] ##STR00277##

[0577] The title compound (800 mg, 96%) was prepared in a manner similar to that in Example A1 step 6 from 3-bromo-5-methylbenzoate and BPD. LC-MS (M+H).sup.+=277.2.

Step 2: methyl 3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylbenzoate

[0578] ##STR00278##

[0579] The title compound (3M) mg, 71%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and methyl 3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate. LC-MS (M+H).sup.+=423.3.

Step 3: 2-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylphenyl)propan-2-ol

[0580] To a solution of methyl 3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylbenzoate (84 mg, 0.10 mmol) in anhydrous THF (3 mL) was added MeLi in Et.sub.2O (1.6 M, 0.63 mL, 1.0 mmol) dropwise at ?78? C. under nitrogen. The mixture was slowly warm to room temperature, then saturated NH.sub.4Cl (50 mL) was added. The mixture was extracted by EtOAc (100 mL). The organic layer was concentrated under reduced pressure and purified by prep-HPLC to give Example A52 (20 mg, 24%). .sup.1H NMR (400 MHz, DMSO-d.sub.6) 8.21 (s, 1H), 8.14 (s, 1H), 7.73 (s, 1H), 7.59 (s, 1H), 7.48 (s, 1H), 7.22 (s, 1H), 6.68 (s, 2H), 5.02 (s, 1H), 4.20-4.11 (m, 1H), 2.89-2.75 (m, 2H), 2.22 (s, 3H), 2.07 (s, 3H), 2.05-1.94 (m, 6H), 1.43 (s, 6H). LCMS (M+H).sup.+=423.3.

Example A53

1-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylbenzyl)-3-(tert-butyl)urea

[0581] ##STR00279##

[0582] To a stirred mixture of 5-(4-(aminomethyl)-3,5-dimethylphenyl)-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine; bis-trifluoroacetic acid (100 mg, 0.158 mmol) and Et.sub.3N (90 mg, 0.89 mmol) in THF (20 mL) was added 2-isocyanato-2-methylpropane (25 mg, 0.252 mmol) at 0? C. The mixture was warmed to room temperature and stirred for 3 h, then concentrated under reduced pressure. The crude was purified by prep-HPLC to give Example A53 (19 mg, 24%). .sup.1H NMR (400 MHz, DMSO-d.sub.6) ? 8.33 (s, 1H), 8.16 (s, 1H), 8.02 (s, 1H), 7.94 (s, 1H), 7.64 (s, 1H), 7.49 (s, 1H), 7.43-7.35 (m, 1H), 6.91 (s, 2H), 4.65-4.52 (m, 1H), 3.59 (t, J=4.6 Hz, 4H), 2.64-2.54 (m, 3H), 2.43 (d, J=5.0 Hz, 6H), 2.37-2.25 (m, 6H). LC-MS (M+H).sup.+=507.4.

Example A54

3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylphenyl)oxetan-3-ol

[0583] ##STR00280##

Step 1: 3-(3-chloro-5-methylphenyl)oxetan-3-ol

[0584] ##STR00281##

[0585] To a solution of 1-bromo-3-chloro-5-methylbenzene (2.0 g, 9.8 mmol) in THF (30 mL) was added n-BuLi in hexane (2.5 M, 3.9 mL, 9.8 mmol) at ?78? C. under nitrogen. After 1 h, oxetan-3-one (1.06 g, 14.7 mmol) was added dropwise. The mixture was stirred for 3 h at ?78? C. and warmed to room temperature. The mixture was poured into water (100 mL) and then extracted with EtOAc (100 mL?3). The combined organic layer was washed with brine (100 mL), dried over Na.sub.2SO.sub.4, filtered and concentrated under vacuum. The crude was purified by jo silica gel column chromatography (PE:EtOAc=3:1) to give the title compound (1.2 g, 62%). LC-MS (M+H).sup.+=199.0.

Step 2: 3-(3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)oxetan-3-ol

[0586] ##STR00282##

[0587] To a solution of 3-(3-chloro-5-methylphenyl)oxetan-3-ol (400 mg, 2.0 mmol) in dioxane (10 mL) was added BPD (667 mg, 2.6 mmol), dichlorobis(tricyclohexylphosphine)palladium(II) (179 mg, 0.24 mmol) and AcOK (297 mg, 3.03 mmol). The mixture was stirred for 16 h at 100? C., cooled to room temperature and poured into water (100 mL). The mixture was extracted with EtOAc (100 mL?3). The combined organic layer was washed with brine (100 mL), dried over Na.sub.2SO.sub.4, filtered and concentrated under vacuum. The crude was purified by silica gel column chromatography (PE:EtOAc=3:1) to give the title compound (184 mg, 31%). LC-MS (M+H).sup.+=291.1.

Step 3: 3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylphenyl)oxetan-3-ol

[0588] To a mixture of 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine (150 mg, 0.43 mmol) in dioxane (9 mL) and water (3 mL) was added 3-(3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)oxetan-3-ol (187 mg, 0.64 mmol), Pd(dppf)Cl.sub.2 (35 mg, 0.04 mmol) and K.sub.2CO.sub.3 (178 mg, 1.29 mmol). The mixture was stirred for 16 h at 95? C., cooled to room temperature then poured into water (100 mL). The mixture was extracted with EtOAc (100 mL?3). The combined organic layer was washed with brine (100 mL), dried over Na.sub.2SO.sub.4, filtered and concentrated under vacuum. The crude was purified by prep-HPLC to give Example A54 (59 mg, 32%). .sup.1H NMR (400 MHz, DMSO-d.sub.6) ? 8.26 (s, 1H), 8.14 (s, 1H), 7.88 (s, 1H), 7.65-7.55 (m, 2H), 7.34 (s, 1H), 6.73 (s, 2H), 6.35 (s, 1H), 4.86-4.63 (m, 4H), 4.20-4.06 (m, 1H), 2.95-2.80 (m, 2H), 2.37 (s, 3H), 2.21 (s, 3H), 2.11-1.91 (m, 6H). LC-MS (M+H).sup.+=437.3.

Example A55

5-(3,5-dimethyl-4-((oxetan-3-ylamino)methyl)phenyl)-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine

[0589] ##STR00283##

Step 1: N-(4-bromo-2,6-dimethylbenzyl)oxetan-3-amine

[0590] ##STR00284##

[0591] To a solution of 4-bromo-2,6-dimethylbenzaldehyde (3.0 g, 14 mmol) in DCM (60 mL) was added oxetan-3-amine (0.85 g, 11.7 mmol) and NaBH(OAc).sub.3 (5.0 g, 23.4 mmol) at room temperature. After 16 h, the mixture was quenched with saturated NaHCO.sub.3 solution (50 mL) and extracted with DCM (50 mL?2). The combined organic layer was washed with brine (50 mL), dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure. The residue was purified by silica gel chromatography (PE/EtOAc=5/1 to 1/1) to give the title compound (2.0 g, 63%). LCMS (M+H).sup.+=270, 272.

Step 2: N-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)oxetan-3-amine

[0592] ##STR00285##

[0593] The title compound (1.5 g, 63%) was prepared in a manner similar to that in Example A1 step 6 from N-(4-bromo-2,6-dimethylbenzyl)oxetan-3-amine and BPD. LCMS (M+H).sup.+=318.2.

Step 3: 5-(3,5-dimethyl-4-((oxetan-3-ylamino)methyl)phenyl)-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine

[0594] Example A55 (310 mg, 24%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and N-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)oxetan-3-amine. .sup.1H NMR (400 MHz, DMSO-d6) ? 8.21 (s, 1H), 8.12 (s, 1H), 7.58 (s, 1H), 7.49-7.44 (m, 2H), 6.67 (s, 2H), 4.67-4.58 (m, 2H), 4.40-4.30 (m, 2H), 4.19-4.09 (m, 1H), 3.96-3.86 (m, 1H), 3.60-3.52 (s, 2H), 2.90-2.80 (m, 2H), 2.36 (s, 6H), 2.21 (s, 3H), 2.11-1.96 (m, 6H). LCMS (M+H).sup.+=464.3.

Example A56

5-(3,5-dimethyl-4-(((1-methyl-1H-pyrazol-3-yl)amino)methyl)phenyl)-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine

[0595] ##STR00286##

Step 1: N-(4-bromo-2,6-dimethylbenzyl)-1-methyl-1H-pyrazol-3-amine

[0596] ##STR00287##

[0597] To a stirred mixture of 4-bromo-2,6-dimethylbenzaldehyde (1.14 g, 5.1 mmol) and 1-methylpyrazol-3-amine (400 mg, 3.9 mmol) in MeOH (5 mL) was added AcOH (50 mg, 0.78 mmol) at room temperature. After 16 h, the mixture was cooled to 0? C. and NaBH.sub.3CN (492 mg, 7.8 mmol) was added. The mixture was warmed to room temperature and stirred for 2 h. then cooled to 0? C. again. Water (5 mL) was added and the precipitate was collected by filtration. The solid was washed with EtOAc (10 mL?3) and dried under vacuum to give the title compound (600 mg, 35%). LC-MS (M+H).sup.+=294.1.

Step 2: N-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)-1-methyl-1H-pyrazol-3-amine

[0598] ##STR00288##

[0599] The title compound (116 mg, 50%) was prepared in a manner similar to that in Example A1 step 6 from N-(4-bromo-2,6-dimethylbenzyl)-1-methyl-1H-pyrazol-3-amine and BPD. LC-MS (M+H).sup.+=342.1.

Step 3: 5-(3,5-dimethyl-4-(((1-methyl-1H-pyrazol-3-yl)amino)methyl)phenyl)-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine

[0600] Example A56 (10 mg, 7%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and N-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)-1-methyl-1H-pyrazol-3-amine. .sup.1H NMR (400 MHz, DMSO-d.sub.6) ? 8.22 (s, 1H), 8.12 (s, 1H), 7.59 (s, 1H), 7.49 (s, 2H), 7.33-7.28 (m, 1H), 6.67 (s, 2H), 5.44-5.40 (m, 1H), 4.98 (t, J=5.6 Hz, 1H), 4.19-4.07 (m, 3H), 3.63 (s, 3H), 2.90-2.81 (m, 2H), 2.36 (s, 6H), 2.20 (s, 3H), 2.12-1.90 (m, 6H). LC-MS (M+H).sup.+=488.3.

Example A57

5-(3,5-dimethyl-4-(((1-methyl-1H-pyrazol-4-yl)amino)methyl)phenyl)-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine

[0601] ##STR00289##

Step 1: N-(4-bromo-2,6-dimethylbenzyl)-1-methyl-1H-pyrazol-4-amine

[0602] ##STR00290##

[0603] The title compound (216 mg, 35%) was prepared in a manner similar to that in Example A56 step 1 from 4-bromo-2,6-dimethylbenzaldehyde and 1-methylpyrazol-4-amine. LC-MS (M+H).sup.+=294.0.

Step 2: N-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)-1-methyl-1H-pyrazol-4-amine

[0604] ##STR00291##

[0605] The title compound (162 mg, 57%) was prepared in a manner similar to that in Example A1 step 6 from N-(4-bromo-2,6-dimethylbenzyl)-1-methyl-1H-pyrazol-4-amine and BPD. LC-MS (M+H).sup.+=342.1.

Step 3: 5-(3,5-dimethyl-4-(((1-methyl-1H-pyrazol-4-yl)amino)methyl)phenyl)-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine

[0606] Example A57 (20 mg, 15%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-H-pyrazol-4-yl)oxy)pyrazin-2-amine and N-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)-1-methyl-1H-pyrazol-4-amine. .sup.1H NMR (400 MHz, DMSO-d.sub.6) ? 8.22 (s, 1H), 8.12 (s, 1H), 7.59 (s, 1H), 7.50 (s, 2H), 7.14 (s, 1H), 6.99 (s, 1H), 6.68 (s, 2H), 4.30-4.22 (m, 1H), 4.19-4.07 (m, 1H), 3.96-3.87 (m, 2H), 3.71 (s, 3H), 2.90-2.81 (m, 2H), 2.35 (s, 6H), 2.20 (s, 3H), 2.11-1.91 (m, 6H). LC-MS (M+H).sup.+=488.3.

Example A58

4-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylphenyl)tetrahydro-2H-pyran-4-ol

[0607] ##STR00292##

Step 1: 4-(3-bromo-5-methylphenyl)tetrahydro-2H-pyran-4-ol

[0608] ##STR00293##

[0609] To a solution of 1,3-dibromo-5-methylbenzene (2.0 g, 8.0 mmol) in THF (5 mL) was added n-BuLi in hexane (1.6 M, 5 mL, 8.0 mmol) at ?78? C. dropwise under N.sub.2. After 0.5 h, tetrahydro-4H-pyran-4-one (960 mg, 9.6 mmol) was added dropwise. After another 1 h, to the mixture was added saturated NH.sub.4Cl (10 mL). After being warmed to room temperature, the mixture was diluted with water (10 mL) and the mixture was extracted with EtOAc (40 mL?2). The combined organic layer was washed with brine (50 mL), dried over Na.sub.2SO.sub.4, filtered and concentrated under vacuum. The crude was purified by prep-TLC (PE:EtOAc=2:1) to give the title compound (1.2 g, 55%). LC-MS (M+H).sup.+=271.1, 273.1.

Step 2: 4-(3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)tetrahydro-2H-pyran-4-ol

[0610] ##STR00294##

[0611] A mixture of 4-(3-bromo-5-methylphenyl)tetrahydro-2H-pyran-4-ol (1.0 g, 3.7 mmol), BPD (1.88 g, 7.4 mmol), Pd(dppf)Cl.sub.2 (302 mg, 0.37 mmol) and AcOK (1.0 g, 11.1 mmol) was in dioxane (30 mL) was heated to reflux under nitrogen for overnight. The mixture was cooled to room temperature then diluted with EtOAc (60 mL). The mixture was washed with brine (30 mL?2), and the combined aqueous layer was extracted with EtOAc (30 mL). The combined organic layer was dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure. The crude was purified by prep-TLC (PE/EtOAc=2:1) to give the title compound (1.0 g, 85%). LC-MS (M+H).sup.+=319.3.

Step 3: 4-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylphenyl)tetrahydro-2H-pyran-4-ol

[0612] Example A58 (10 mg, 7%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and 4-(3-jo methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)tetrahydro-2H-pyran-4-ol. .sup.1H NMR (400 MHz, DMSO-d6) ? 8.19 (s, 1H), 8.09 (s, 1H), 7.7 (s, 1H), 7.47 (s, 1H), 7.2 (s, 1H), 6.65 (s, 2H), 4.95 (s, 1H), 4.06-4.07 (m, 1H), 3.77-3.64 (m, 4H), 2.82 (d, J=9.2, 2H), 2.29 (s, 3H), 2.15 (s, 3H), 2.0-1.9 (m, 7H), 1.5 (d, J=13.6). LC-MS (M+H).sup.+=465.2.

Compound A59

(R)-3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-(3-methylmorpholino)phenyl)oxetan-3-ol

[0613] ##STR00295##

Step 1: (R)-4-(3,5-dibromophenyl)-3-methylmorpholine

[0614] ##STR00296##

[0615] To a solution of 1,3-dibromo-5-iodobenzene (2.0 g, 5.5 mmol) in dioxane (20 mL) was added (R)-3-methylmorpholine (558 mg, 5.5 mmol), Pd.sub.2(dba).sub.3 (250 mg, 0.28 mmol), XantPhos (310 mg, 0.55 mmol) and Cs.sub.2CO.sub.3 (2.0 g, 6.1 mmol) under nitrogen and the mixture was heated to reflux for overnight. The mixture was cooled to room temperature and concentrated in vacuo. The crude was purified by silica gel chromatography (PE:EtOAc=20:1) to give the title compound (1.0 g, 54%). LC-MS (M+H).sup.+=335.9, 337.9.

Step 2: (R)-3-(3-bromo-5-(3-methylmorpholino)phenyl)oxetan-3-ol

[0616] ##STR00297##

[0617] The title compound (150 mg, 31%) was prepared in a manner similar to that in Example A54 step 1 from (R)-4-(3,5-dibromophenyl)-3-methylmorpholine and oxetan-3-one. LC-MS (M+H).sup.+=328.0.

Step 3: (R)-3-(3-(3-methylmorpholino)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)oxetan-3-ol

[0618] ##STR00298##

[0619] The title compound (147 mg, 85%) was prepared in a manner similar to that in Example A1 step 6 from (R)-3-(3-bromo-5-(3-methylmorpholino)phenyl)oxetan-3-ol and BPD. LC-MS (M+H).sup.+=376.2.

Step 4: (R)-3-(3-5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-(3-methylmorpholino)phenyl)oxetan-3-ol

[0620] Example A59 (10 mg, 5%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and (R)-3-(3-(3-methylmorpholino)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)oxetan-3-ol. .sup.1H NMR (400 MHz, DMSO-d6) ? 8.22 (s, 1H), 8.08 (s, 1H), 7.53 (s, 1H), 7.48 (s, 1H), 7.23 (s, 1H), 6.97 (s, 1H), 6.67 (s, 2H), 6.25 (s, 1H), 4.76-4.60 (m, 4H), 4.10-3.98 (m, 1H), 3.91-3.78 (m, 2H), 3.75-3.59 (m, 2H), 3.58-3.48 (m, 1H), 3.22-3.12 (m, 1H), 3.07-2.95 (m, 1H), 2.87-2.76 (m, 2H), 2.17 (s, 3H), 2.05-1.79 (m, 6H), 1.00-0.90 (m, 3H). LC-MS (M+H).sup.+=522.2.

Example A60

5-(3,5-dimethyl-4-(((3-methyloxetan-3-yl)amino)methyl)phenyl)-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine

[0621] ##STR00299##

Step 1: N-(4-bromo-2,6-dimethylbenzyl)-3-methyloxetan-3-amine

[0622] ##STR00300##

[0623] The title compound (1.6 g, 81%) was prepared in a manner similar to that in compound A55 step 1 from 4-bromo-2,6-dimethylbenzaldehyde and 3-methyloxetan-3-amine. LCMS (M+H).sup.+=284, 286.

Step 2: N-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)-3-methyloxetan-3-amine

[0624] ##STR00301##

[0625] The title compound (0.70 g, 38%) was prepared in a manner similar to that in compound A1 step 6 from N-(4-bromo-2,6-dimethylbenzyl)-3-methyloxetan-3-amine and BPD. LCMS (M+H).sup.+=332.2.

Step 3: 5-(3,5-dimethyl-4-(((3-methyloxetan-3-yl)amino)methyl)phenyl)-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine

[0626] Example A60 (105 mg, 52%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and N-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)-3-methyloxetan-3-amine. .sup.1H NMR (400 MHz, DMSO-d6) ? 8.21 (s, 1H), 8.12 (s, 1H), 7.59 (s, 1H), 7.50-7.42 (m, 2H), 6.67 (s, 2H), 4.60-4.50 (m, 2H), 4.30-4.21 (m, 2H), 4.19-4.07 (m, 1H), 3.59 (s, 2H), 2.91-2.82 (m, 2H), 2.38 (s, 6H), 2.21 (s, 3H), 2.11-1.96 (m, 6H), 1.48 (s, 3H). LCMS (M+H).sup.+=478.3.

Example A61A/A61B

(S)-5-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylphenyl)pyrrolidin-2-one & (R)-5-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylphenyl)pyrrolidin-2-one

[0627] ##STR00302##

Step 1: 4-(3-bromo-5-methylphenyl)-2-hydroxy-4-oxobutanoic acid

[0628] ##STR00303##

[0629] To a solution of 1-(3-bromo-5-methylphenyl)ethanone (4.26 g, 19.6 mmol) in AcOH (70 mL) was added 2-oxoacetic acid (2.90 g, 19.6 mmol) at room temperature. The mixture was stirred for 8 h at 120? C. under nitrogen. The mixture was cooled to room temperature and concentrated under reduced pressure. The residue was purified by silica gel chromatography (PE:EtOAc=2:1) to give the title compound (2.24 g, 40%). LCMS (M+H).sup.+=286.9.

Step 2: 4-(3-bromo-5-methylphenyl)-4-oxobut-2-enoic acid

[0630] ##STR00304##

[0631] To a solution of 4-(3-bromo-5-methylphenyl)-2-hydroxy-4-oxobutanoic acid (2.8 g, 7.87 mmol) in AcOH (60 mL) was added concentrated HCl (20 mL) dropwise at room temperature.

[0632] The mixture was stirred for overnight at 120? C. under nitrogen atmosphere. The mixture was cooled to room temperature and diluted with water (50 mL). The mixture was extracted with ethyl acetate (200 mL?3). The combined organic layer was washed with brine (100 mL), dried over Na.sub.2SO.sub.4 and filtered. The solvent was evaporated under reduced pressure to give the title compound (1.8 g, 84%). LCMS (M+H).sup.+=266.6.

Step 3: 4-(3-bromo-5-methylphenyl)-4-oxobutanoic acid

[0633] ##STR00305##

[0634] To a stirred a solution of 4-(3-bromo-5-methylphenyl)-4-oxobut-2-enoic acid (2.0 g, 6.63 mmol) in AcOH (18 mL) and H.sub.2O (6 mL) was added Zn powder (500 mg, 7.26 mmol) at room temperature. After 3 h, the mixture diluted with of water (50 mL), and filtered. The solid with rinsed with EtOAc (10 mL). The filtrate was extracted with ethyl acetate (60 mL?3). The combined organic layer was washed with brine, dried over Na.sub.2SO.sub.4 and filtered. The solvent was evaporated under reduced pressure and the residue was purified by silica gel chromatography (PE:EtOAc=3:1) to give the title compound (1.6 g, 89%). LCMS (M+H).sup.+=270.9.

Step 4: 5-(3-bromo-5-methylphenyl)pyrrolidin-2-one

[0635] ##STR00306##

[0636] To a solution of 4-(3-bromo-5-methylphenyl)-4-oxobutanoic acid (400 mg, 1.47 mmol) in EtOH (10 mL) was added NH.sub.40Ac (7.2 g, 88.4 mmol) and NaBH.sub.2CN (488.0 mg, 7.38 mmol) in portions at room temperature. The mixture was stirred for 5 h at 80? C. under nitrogen. The mixture was cooled to room temperature and diluted with water (50 mL). The mixture was extracted with ethyl acetate (50 mL?3). The combined organic layer was washed with brine (50 mL), dried over Na.sub.2SO.sub.4 and filtered. The solvent was evaporated under reduced pressure, the residue was purified by prep-HPLC to give the title compound (246 mg, 66%). LCMS (M+H).sup.+=254.0.

Step 5: 5-(3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyrrolidin-2-one

[0637] ##STR00307##

[0638] The title compound (149 mg, 89%) was prepared in a manner similar to that in Example A1 step 6 from 5-(3-bromo-5-methylphenyl)pyrrolidin-2-one and BPD. LC-MS (M+H).sup.+=302.2.

Step 6

(S)-5-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylphenyl)pyrrolidin-2-one & (R)-5-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylphenyl)pyrrolidin-2-one

[0639] Examples A61A/A61B were prepared in a manner similar to that in Example A1 step 7 from 5-(3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyrrolidin-2-one and 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine, then the isomers were separated by chiral-HPLC. Analytical chiral-HPLC condition: CHIRALPAK 1C3, 4.6?50 mm; (Hexane:DCM=3:1, contains 0.1% Et.sub.2NH):IPA=1:1; 1 mL/min; 25? C.

Example A61A

[0640] ((R)-5-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylphenyl)pyrrolidin-2-one): (34 mg, 20%) .sup.1H NMR (400 MHz, DMSO-d.sub.6) ? 8.24 (s, 1H), 8.12 (s, 1H), 8.07 (s, 1H), 7.60-7.53 (m, 3H), 7.04 (s, 1H), 6.74 (s, 2H), 4.69-4.59 (m, 1H), 4.20-4.10 (m, 1H), 2.89-2.79 (m, 2H), 2.48-2.40 (m, 1H), 2.33 (s, 3H), 2.29-2.20 (m, 2H), 2.20 (s, 3H), 2.12-1.91 (m, 6H), 1.85-1.73 (m, 1H). LC-MS (M+H).sup.+=448.3. Chiral HPLC: tR=3.50 min.

Example A61B

[0641] ((S)-5-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylphenyl)pyrrolidin-2-one): (30 mg, 18%) .sup.1H NMR (400 MHz, DMSO-d.sub.6) ? 8.24 (s, 1H), 8.12 (s, 1H), 8.07 (s, 1H), 7.60-7.53 (m, 3H), 7.04 (s, 1H), 6.74 (s, 2H), 4.69-4.59 (m, 1H), 4.20-4.10 (m, 1H), 2.89-2.79 (m, 2H), 2.48-2.40 (m, 1H), 2.33 (s, 3H), 2.29-2.20 (m, 2H), 2.20 (s, 3H), 2.12-1.91 (m, 6H), 1.85-1.73 (m, 1H). LC-MS (M+H).sup.+=448.3. Chiral HPLC: tR=5.00 min.

Example A62

5-(4-[[(dimethylsulfamoyl)amino]methyl]-3,5-dimethylphenyl)-3-[[1-(1-methylpiperidin-4-yl)pyrazol-4-yl]oxy]pyrazin-2-amine

[0642] ##STR00308##

Step 1: [[(4-bromo-2,6-dimethylphenyl)methyl]sulfamoyl]dimethylamine

[0643] ##STR00309##

[0644] The title compound (375 mg, 71%) was prepared in a manner similar to that in Example A11 step 2 from 1-(4-bromo-2,6-dimethylphenyl)methanamine and dimethylsulphamoyl chloride. LC-MS (M+H).sup.+=320.9.

Step 2: ([[2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methyl]sulfamoyl)dimethylamine

[0645] ##STR00310##

[0646] The title compound (168 mg, 59%) was prepared in a manner similar to that in Example A1 step 6 from [[(4-bromo-2,6-dimethylphenyl)methyl]sulfamoyl]dimethylamine and BPD. LC-MS (M+H).sup.+=369.0.

Step 3: 5-(4-[[(dimethylsulfamoyl)amino]methyl]-3,5-dimethylphenyl)-3-[[1-(1-methylpiperidin-4-yl)pyrazol-4-yl]oxy]pyrazin-2-amine

[0647] Example A62 (35 mg, 17%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and ([[2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methyl]sulfamoyl)dimethylamine. .sup.1H NMR (300 MHz, DMSO-d.sub.6) ? 8.22 (s, 1H), 8.10 (s, 1H), 7.57 (s, 1H), 7.48 (s, 2H), 7.27 (t, J=5.4 Hz, 1H), 6.69 (s, 2H), 4.18-4.08 (m, 1H), 4.08-4.02 (m, 2H), 2.90-2.78 (m, 2H), 2.69 (s, 6H), 2.36 (s, 6H), 2.19 (s, 3H), 2.13-1.90 (m, 6H). LC-MS (M+H).sup.+=515.2.

Example A63

3-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylphenyl)oxetan-3-ol

[0648] ##STR00311##

Step 1: 3-(4-chloro-2,6-dimethylphenyl)oxetan-3-ol

[0649] ##STR00312##

[0650] To a stirred solution of 5-chloro-2-iodo-1,3-dimethylbenzene (798 mg, 3.0 mmol) in anhydrous THF (10 mL) was added n-BuLi in hexanes (2.5 M, 1.2 mL, 3.0 mmol) dropwise at?78? C. under nitrogen. After 3 h, oxetan-3-one (216 mg, 3.0 mmol) was added. The mixture was warm to room temperature within 30 min, then saturated NH.sub.4Cl solution (50 mL) was added. The mixture was extracted with EtOAc (50 mL). The organic layer was separated, dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure. The crude was purified by prep-TLC to give the title compound (250 mg, 39%). LC-MS (M-OH).sup.+=195.2.

Step 2: 3-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)oxetan-3-ol

[0651] ##STR00313##

[0652] A mixture of 3-(4-chloro-2,6-dimethylphenyl)oxetan-3-ol (250 mg, 1.17 mmol), BPD (444 mg, 1.75 mmol), dichlorobis(tricyclohexylphosphine)palladium(II) (258 mg, 0.35 mmol) and AcOK (344 mg, 3.51 mmol) in dioxane (30 mL) was heated to reflux under nitrogen for overnight. The mixture was cooled to room temperature and concentrated under vacuum. The crude was purified by silica gel chromatography (PE:EtOAc=10:1) to give the title compound (350 mg, 98%). LC-MS (M-OH).sup.+=287.2.

Step 3: 3-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylphenyl)oxetan-3-ol

[0653] Example A63 (55 mg, 41%) was prepared in a manner similar to that in Example A1 step 7 from 3-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)oxetan-3-ol and 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine. .sup.1H NMR (400 MHz, DMSO-d.sub.6) ? 8.22 (s, 1H), 8.11 (s, 1H), 7.58 (s, 1H), 7.44 (s, 2H), 6.71 (s, 2H), 6.13 (s, 1H), 5.05 (s, 2H), 4.58 (s, 2H), 4.18-4.04 (m, 1H), 2.90-2.80 (m, 2H), 2.21 (s, 3H), 2.13 (s, 6H), 2.08-1.94 (m, 6H). LCMS (M+H).sup.+=451.2.

Example A64

1-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylbenzyl)-3-(1-(trifluoromethyl)cyclopropyl)urea

[0654] ##STR00314##

[0655] A mixture of 1-(trifluoromethyl)cyclopropane-1-carboxylic acid (18 mg, 0.12 mmol), diphenylphosphonic azide (33 mg, 0.12 mmol) and Et.sub.3N (12 mg, 0.12 mmol) in toluene (1 mL) was heated to refluxed for 2 h. The mixture was concentrated under reduced pressure and re-dissolved in THF (1 mL). The solution was added dropwise to a solution of 5-(4-(aminomethyl)-3,5-dimethylphenyl)-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine; bis-trifluoroacetic acid (50 mg, 0.079 mmol) and Et.sub.3N (24 mg, 0.24 mmol) in THF (1 mL) at 0? C. After 3 h, EtOAc (10 mL) was added and the organic layer was successively washed with H.sub.2O (5 mL), brine (5 mL), dried over Na.sub.2SO.sub.4, filtered and concentrated under vacuum. The residue was purified by prep-HPLC to give Example A64 (24 mg, 55%), 1H NMR (400 MHz, DMSO-d6) ? 8.21 (s, 1H), 8.12 (s, 1H), 7.58 (s, 1H), 7.49 (s, 2H), 6.70 (s, 2H), 6.58 (s, 1H), 5.97 (s, 1H), 4.21 (s, 2H), 4.20-4.11 (m, 1H), 2.88-2.83 (m, 2H), 2.33 (s, 6H), 2.21 (s, 3H), 2.11-1.94 (m, 6H), 1.16 (s, 2H), 1.02 (s, 2H). LC-MS (M+H).sup.+=559.3.

Example A65

1-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylphenyl)cyclopentan-1-ol

[0656] ##STR00315##

Step 1: 1-(3-bromo-5-methylphenyl)cyclopentan-1-ol

[0657] ##STR00316##

[0658] The title compound (1.5 g, 74%) was prepared in a manner similar to that in Example A54 step 1 from 1,3-dibromo-5-methylbenzene and cyclopentanone. LCMS (M?OH).sup.+=237,239.

Step 2: 1-(3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclopentan-1-ol

[0659] ##STR00317##

[0660] The title compound (1.2 g, 71%) was prepared in a manner similar to that in Example A1 step 6 from 1-(3-bromo-5-methylphenyl)cyclopentan-1-ol and BPD. LCMS (M?OH)+=285.

Step 3: 1-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylphenyl)cyclopentan-1-ol

[0661] Example A65 (50 mg, 27%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and 1-(3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclopentan-1-ol. .sup.1H NMR (400 MHz, DMSO-d6) ? 8.17 (s, 1H), 8.08 (s, 1H), 7.68 (s, 1H), 7.54 (s, 1H), 7.44 (s, 1H), 7.18 (s, 1H), 6.64 (s, 2H), 4.71 (s, 1H), 4.14-4.02 (m, 1H), 2.90-2.80 (m, 2H), 2.28 (s, 3H), 2.19 (s, 3H), 2.12-1.91 (m, 6H), 1.86-1.66 (m, 8H). LCMS (M+H).sup.+=449.4.

Example A66

5-(3,5-dimethyl-4-morpholinophenyl)-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine

[0662] ##STR00318##

Step 1: 4-(4-chloro-2,6-dimethylphenyl)morpholine

[0663] ##STR00319##

[0664] A mixture of 2-bromo-5-chloro-1,3-dimethylbenzene (1.1 g, 5.0 mmol), morpholine (522 mg, 6.0 mmol), XantPhos (286 mg, 0.50 mmol), Pd(dba).sub.2 (287 mg, 0.50 mmol) and t-BuOK (1.12 g, 10 mmol) in toluene (30 mL) was heated to reflux overnight under nitrogen. The mixture was cooled to room temperature, concentrated under vacuum then diluted with water (100 mL). The mixture was extracted with DCM (100 mL). The organic layer was separated and concentrated under reduced pressure. The crude was purified by prep-TLC (PE:EA=10:1) to jo give the title compound (200 mg, 18%). LC-MS (M+H).sup.+=226.1.

Step 2: 4-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)morpholine

[0665] ##STR00320##

[0666] A mixture of 4-(4-chloro-2,6-dimethylphenyl)morpholine (100 mg, 0.44 mmol), BPD (168 mg, 0.66 mmol), dichlorobis(tricyclohexylphosphine)palladium(II) (96 mg, 0.13 mmol) and AcOK (130 mg, 1.32 mmol) in dioxane (10 mL) was heated to reflux for overnight under nitrogen. The mixture was cooled to room temperature and concentrated under reduced pressure. The crude was purified by silica gel chromatography (PE:EA=10:1) to give the title compound (130 mg, 93%). LC-MS (M+H).sup.+=228.1.

Step 3: 5-(3,5-dimethyl-4-morpholinophenyl)-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine

[0667] Example A66 (28 mg, 30%) was prepared in a manner similar to that in Example A1 step 7 from 4-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)morpholine and 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine. .sup.1H NMR (400 MHz, DMSO-d.sub.6) ? 8.17 (s, 1H), 8.11 (s, 1H), 7.58 (s, 1H), 7.45 (s, 2H), 6.64 (s, 2H), 4.15-4.10 (m, 1H), 3.69-3.67 (m, 4H), 3.01-2.97 (m, 4H), 2.87-2.85 (m, 2H), 2.32 (s, 6H), 2.21 (s, 3H), 2.09-1.96 (m, 6H). LCMS (M+H).sup.+=464.2.

Example A67

N-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylbenzyl)oxazol-2-amine

[0668] ##STR00321##

Step 1: N-(4-bromo-2,6-dimethylbenzyl)oxazol-2-amine

[0669] ##STR00322##

[0670] To a solution of 4-bromo-2,6-dimethylbenzaldehyde (1.0 g, 4.72 mmol) in dioxane (30 mL) was added 4-methylbenzenesulfonohydrazide (877 mg, 4.72 mmol). The solution was stirred for 3 h at 60? C. and cooled to room temperature, then t-BuOLi (755 mg, 9.44 mmol), CuI (116 mg, 0.61 mmol) and oxazol-2-amine(265 mg, 3.16 mmol) was added. The mixture was stirred for 3 h at 100? C. under nitrogen and cooled to room temperature. The mixture was poured into water (100 mL) and then extracted with EtOAc (100 mL?3). The combined organic layer was washed with brine (100 mL), dried over Na.sub.2SO.sub.4, filtered and concentrated under vacuum. The crude was purified by silica gel chromatography (PE:EtOAc=1:1) to give the title compound (580 mg, 44%). LC-MS (M+H).sup.+=281.0, 283.0.

Step 2: N-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)oxazol-2-amine

[0671] ##STR00323##

[0672] The title compound (500 mg, 74%) was prepared in a manner similar to that in Example A1 step 6 from N-(4-bromo-2,6-dimethylbenzyl)oxazol-2-amine and BPD. LC-MS (M+H).sup.+=329.3.

Step 3: N-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylbenzyl)oxazol-2-amine

[0673] Example A67 (62 mg, 30%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and N-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)oxazol-2-amine. .sup.1H NMR (400 MHz, DMSO-d.sub.6) ? 8.18 (s, 1H), 8.07 (s, 1H), 7.55 (s, 1H), 7.45 (s, 2H), 7.37 (s, 1H), 7.17 (s, 1H), 6.73 (s, 1H), 6.66 (s, 2H), 4.30 (s, 2H), 4.20-4.03 (m, 1H), 2.92-2.82 (m, 2H), 2.32 (s, 6H), 2.23 (s, 3H), 2.17-1.90 (m, 6H). LC-MS (M+H).sup.+=475.3.

Example A68

5-(3,5-dimethyl-4-((1-methyl-1H-1,2,4-triazol-3-yl)amino)methyl)phenyl)-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine

[0674] ##STR00324##

Step 1: N-(4-bromo-2,6-dimethylbenzyl)-1-methyl-1H-1,2,4-triazol-3-amine

[0675] ##STR00325##

[0676] The title compound (400 mg, 29%) was prepared in a manner similar to that in Example A67 step 1 from 4-bromo-2,6-dimethylbenzaldehyde and 1-methyl-1H-1,2,4-triazol-3-amine. LC-MS (M+H).sup.+=295.1, 297.2.

Step 2: N-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)-1-methyl-1H-1,2,4-triazol-3-amine

[0677] ##STR00326##

[0678] The title compound (290 mg, 62%) was prepared in a manner similar to that in Example A1 step 7 from N-(4-bromo-2,6-dimethylbenzyl)-1-methyl-1H-1,2,4-triazol-3-amine and BPD. LC-MS (M+H).sup.+=343.3.

Step 3: 5-(3,5-dimethyl-4-(((1-methyl-1H-1,2,4-triazol-3-yl)amino)methyl)phenyl)-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine

[0679] Example A68 (66 mg, 32%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and N-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)-1-methyl-1H-1,2,4-triazol-3-amine. .sup.1H NMR (400 MHz, DMSO-d.sub.6) ? 8.22 (s, 1H), 8.12 (s, 1H), 7.97 (s, 1H), 7.60 (s, 1H), 7.47 (s, 2H), 6.68 (s, 2H), 5.80 (s, 1H), 4.24 (s, 2H), 4.21-4.10 (m, 1H), 3.66 (s, 3H), 3.00-2.83 (m, 2H), 2.37 (s, 6H), 2.27 (s, 3H), 2.22-1.92 (m, 6H). LC-MS (M+H).sup.+=489.3.

Example A69

3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylphenyl)tetrahydrofuran-3-ol

[0680] ##STR00327##

Step 1: 3-(3-bromo-5-methylphenyl)oxolan-3-ol

[0681] ##STR00328##

[0682] The title compound (434 mg, 44%) was prepared in a manner similar to that in Example A54 step 1 from 1,3-dibromo-5-methylbenzene and dihydrofuran-3-one. LC-MS (M?OH).sup.+=239.0.

Step 2: 3-(3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)tetrahydrofuran-3-ol

[0683] ##STR00329##

[0684] The title compound (89 mg, 78%) was prepared in a manner similar to that in Example A1 step 6 from 3-(3-bromo-5-methylphenyl)oxolan-3-ol and BPD. LC-MS (M?OH)+=287.3.

Step 3: 3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylphenyl)tetrahydrofuran-3-ol

[0685] Example A69 (25 mg, 17%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and 3-(3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)tetrahydrofuran-3-ol. .sup.1H NMR (400 MHz, DMSO-d.sub.6) ? 8.24 (s, 1H), 8.13 (s, 1H), 7.76 (s, 1H), 7.59 (s, 1H), 7.54 (s, 1H), 7.24 (s, 1H), 6.71 (s, 2H), 5.39 (s, 1H), 4.17-4.05 (m, 1H), 4.06-3.94 (m, 2H), 3.83-3.72 (m, 2H), 2.92-2.82 (m, 2H), 2.34 (s, 3H), 2.32-2.23 (m, 1H), 2.21 (s, 3H), 2.15-1.91 (m, 7H). LC-MS (M+H).sup.+=451.3.

Example A70

2-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylphenyl)butan-2-ol

[0686] ##STR00330##

Step 1: 2-(3-bromo-5-methylphenyl)butan-2ol

[0687] ##STR00331##

[0688] The title compound (447 mg, 41%) was prepared in a manner similar to that in Example A54 step 1 from 1,3-dibromo-5-methylbenzene and butan-2-one. LC-MS (M?OH).sup.+=224.9.

Step 2: 2-(3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)butan-2-ol

[0689] ##STR00332##

[0690] The title compound (207 mg, 90%) was prepared in a manner similar to that in Example A1 step 6 from 2-(3-bromo-5-methylphenyl)butan-2-ol and BPD. LC-MS (M?OH).sup.+=273.1.

Step 3: 2-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylphenyl)butan-2-ol

[0691] Example A70 (20 mg, 19%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and 2-(3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)butan-2-ol. .sup.1H NMR (400 MHz, DMSO-d.sub.6) ? 8.21 (s, 1H), 8.14 (s, 1H), 7.69 (s, 1H), 7.59 (s, 1H), 7.47 (s, 1H), 7.17 (s, 1H), 6.65 (s, 2H), 4.80 (s, 1H), 4.17-4.05 (m, 1H), 2.90-2.82 (m, 2H), 2.33 (s, 3H), 2.21 (s, 3H), 2.11-1.92 (m, 6H), 1.77-1.62 (m, 2H), 1.40 (s, 3H), 0.70 (t, J=7.3 Hz, 3H). LC-MS (M+H).sup.+=437.3.

Example A71

N-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylbenzyl)morpholine-4-sulfonamide

[0692] ##STR00333##

Step 1: N-(4-bromo-2,6-dimethylbenzyl)morpholine-4-sulfonamide

[0693] ##STR00334##

[0694] The title compound (295 mg, 62%) was prepared in a manner similar to that in Example A11 step 2 from 1-(4-bromo-2,6-dimethylphenyl)methanamine hydrochloride and morpholine-4-sulfonyl chloride. LC-MS (M+H).sup.+=362.9.

Step 2: N-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)morpholine-4-sulfonamide

[0695] ##STR00335##

[0696] The title compound (130 mg, 47%) was prepared in a manner similar to that in Example A1 step 6 from N-(4-bromo-2,6-dimethylbenzyl)morpholine-4-sulfonamide and BPD. LC-MS (M+H).sup.+=411.1.

Step 3: N-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2,6-dimethylbenzyl)morpholine-4-sulfonamide

[0697] Example A71 (19 mg, 13%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and N-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)morpholine-4-sulfonamide. .sup.1H NMR (400 MHz, DMSO-d6) ? 8.23 (s, 1H), 8.12 (s, 1H), 7.60 (s, 1H), 7.50 (s, 3H), 6.71 (s, 2H), 4.22-4.12 (m, 1H), 4.12-4.07 (m, 2H), 3.59-3.52 (m, 4H), 3.05-2.98 (m, 4H), 2.94-2.87 (m, 2H), 2.38 (s, 6H), 2.25 (s, 3H), 2.17-2.10 (m, 2H), 2.10-1.92 (m, 4H). LC-MS (M+H).sup.+=557.4.

Example A72

3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-morpholinophenyl)oxetan-3-ol

[0698] ##STR00336##

Step 1: 4-(3,5-dibromophenyl)morpholine

[0699] ##STR00337##

[0700] The title compound (1.2 g, 37%) was prepared in a manner similar to that in Example A59 step 1 from 1,3-dibromo-5-iodobenzene and morpholine. LCMS (M+H).sup.+=322.

Step 2: 3-(3-bromo-5-morpholinophenyl)oxetan-3-ol

[0701] ##STR00338##

[0702] The title compound (0.75 g, 64%) was prepared in a manner similar to that in Example A54 step 1 from 4-(3,5-dibromophenyl)morpholine and oxetan-3-one. LCMS (M+H).sup.+=314, 316.

Step 3: 3-(3-morpholino-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)oxetan-3-ol

[0703] ##STR00339##

[0704] The title compound (0.73 g, 85%) was prepared in a manner similar to that in Example A1 step 6 from 3-(3-bromo-5-morpholinophenyl)oxetan-3-ol and BPD. LCMS (M+H).sup.+=362.

Step 4: 3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-morpholinophenyl)oxetan-3-ol

[0705] Example A72 (100 mg, 51%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and 3-(3-morpholino-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)oxetan-3-ol. .sup.1H NMR (400 MHz, DMSO-d6) ? 8.28 (s, 1H), 8.14 (s, 1H), 7.58 (s, 1H), 7.56 (s, 1H), 7.33 (s, 1H), 7.06 (s, 1H), 6.73 (s, 2H), 6.31 (s, 1H), 4.79-4.69 (m, 4H), 4.16-4.04 (m, 1H), 3.81-3.72 (m, 4H), 3.22-3.12 (m, 4H), 2.91-2.83 (m, 2H), 2.22 (s, 3H), 2.11-1.94 (m, 6H). LCMS (M+H).sup.+=508.5.

Example A73

3-(5-(5-amino-6-(1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yloxy)pyrazin-2-yl)-2,3-dimethylphenyl)oxetan-3-ol

[0706] ##STR00340##

Step 1: 1-bromo-5-chloro-2,3-dimethylbenzene

[0707] ##STR00341##

[0708] The title compound (385 mg, 46%) was prepared in manner similar to that in Example A84 step 1 from 3-bromo-4,5-dimethylaniline.

Step 2: 3-(5-chloro-2,3-dimethylphenyl)oxetan-3-ol

[0709] ##STR00342##

[0710] The title compound (304 mg, 82%) was prepared in a manner similar to that in Example A54 step 1 from 1-bromo-5-chloro-2,3-dimethylbenzene and oxetan-3-one. LC-MS (M?OH).sup.+=195.0.

Step 3: 3-(2,3-dimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)oxetan-3-ol

[0711] ##STR00343##

[0712] The titled compound (264 mg, 65%) was prepared in a manner similar to that in Example A54 step 2 from 3-(5-chloro-2,3-dimethylphenyl)oxetan-3-ol. LC-MS (M?OH).sup.+=287.1.

Step 4: 3-(5-(5-amino-6-(1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yloxy)pyrazin-2-yl)-2,3-dimethylphenyl)oxetan-3-ol

[0713] Example A73 (23 mg, 19%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and 3-(2,3-dimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)oxetan-3-ol. .sup.1H NMR (300 MHz, DMSO-d.sub.6) ? 8.24 (s, 1H), 8.07 (s, 1H), 7.63-7.54 (m, 2H), 7.50 (s, 1H), 6.64 (s, 2H), 6.10 (s, 1H), 5.01 (d, J=6.7 Hz, 2H), 4.71 (d, J=6.7 Hz, 2H), 4.15-4.01 (m, 1H), 2.92-2.80 (m, 2H), 2.24 (s, 3H), 2.19 (s, 3H), 2.10-1.90 (m, 9H). LC-MS (M+H).sup.+=451.3.

Example A74A/A74B

[0714] (S)-3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylphenyl)tetrahydrofuran-3-ol & (R)-3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylphenyl)tetrahydrofuran-3-ol

##STR00344##

[0715] Example A69 (700 mg) was separated by chiral-HPLC to give Example A74A/A74B. Analytical chiral-HPLC condition: CHIRALPAK IA3, 4.6?50 mm, 3 ?m; (Hexane:DCM=3:1, contains 0.1% Et.sub.2NH):EtOH=9:1; 1 mL/min: 25? C.

Example A74A

[0716] ((S)-3-(3-(5-amino-64(1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylphenyl)tetrahydrofuran-3-ol): (228 mg, 33%).sup.1H NMR (400 MHz, DMSO-d.sub.6) ? 8.22 (s, 1H), 8.12 (s, 1H), 7.74 (s, 1H), 7.57 (s, 1H), 7.52 (s, 1H), 7.24 (s, 1H), 6.68 (s, 2H), 5.37 (s, 1H), 4.15-4.03 (m, 1H), 4.04-3.92 (m, 2H), 3.81-3.70 (m, 2H), 2.91-2.82 (m, 2H), 2.34 (s, 3H), 2.32-2.23 (m, 1H), 2.21 (s, 3H), 2.15-1.91 (m, 7H). LC-MS (M+H).sup.+=451.3. Chiral HPLC: tR=1.59 min.

Example A74B

[0717] ((R)-3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylphenyl)tetrahydrofuran-3-ol): (252 mg, 36%).sup.1H NMR (400 MHz, DMSO-d.sub.6) .sup.1H NMR (300 MHz, DMSO-d.sub.6) ? 8.24 (s, 1H), 8.13 (s, 1H), 7.76 (s, 1H), 7.59 (s, 1H), 7.54 (s, 1H), 7.24 (s, 1H), 6.69 (s, 2H), 5.38 (s, 1H), 4.17-4.05 (m, 1H), 4.06-3.94 (m, 2H), 3.83-3.72 (m, 2H), 2.92-2.82 (m, 2H), 2.34 (s, 3H), 2.32-2.23 (m, 1H), 2.21 (s, 3H), 2.15-1.91 (m, 7H). LC-MS (M+H).sup.+=451.3. Chiral HPLC: tR=2.08 min.

Example A75

5-(4-(3,6-dihydro-2H-pyran-4-yl)-3,5-dimethylphenyl)-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine

[0718] ##STR00345##

Step 1: 4-(4-bromo-2,6-dimethylphenyl)-3,6-dihydro-2H-pyran

[0719] ##STR00346##

[0720] A mixture of 5-bromo-2-iodo-1,3-dimethylbenzene (1.55 g, 5.0 mmol), 2-(3,6-dihydro-2H-pyran-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (1.15 g, 5.5 mmol), Pd(dppf)Cl.sub.2.Math.DCM (204 mg, 0.25 mmol) and K.sub.2CO.sub.3(2.07 g, 15 mmol) in dioxane (20 mL) and water (2 mL) was stirred at 100? C. overnight under nitrogen. The mixture was cooled to room temperature, diluted with water (100 mL) and extracted by DCM (100 mL). The organic layer was dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure. The residue was purified by silica gel prep-TLC (PE:EtOAc=10:1) to give the title compound (772 mg, 58%). LC-MS (M+H).sup.+=267.0, 269.1.

Step 2: 2-(4-(3,6-dihydro-2H-pyran-4-yl)-3,5-dimethylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

[0721] ##STR00347##

[0722] 4-(4-bromo-2,6-dimethylphenyl)-3,6-dihydro-2H-pyran (772 mg, 2.9 mmol), BPD (810 mg, 3.19 mmol), Pd(dppf)Cl.sub.2.Math.DCM (118 mg, 0.145 mmol) and AcOK (853 mg, 8.7 mmol) was added in dioxane (10 mL) under nitrogen. The reaction mixture was heated to reflux overnight. The mixture was cooled to room temperature and concentrated, then the residue was purified by silica gel column chromatography (PE:EtOAc=10:1) to give the title compound (900 mg, 98%). LC-MS (M+H).sup.+=315.3.

Step 3: 5-(4-(3,6-dihydro-2H-pyran-4-yl)-3,5-dimethylphenyl)-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine

[0723] Example A75 (57 mg, 62%) was prepared in a manner similar to that in Example A1 step 7 from 2-(4-(3,6-dihydro-2H-pyran-4-yl)-3,5-dimethylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane and 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine. .sup.1H NMR (400 MHz, DMSO-d.sub.5) ? 8.14 (s, 1H), 8.05 (s, 1H), 7.53 (s, 1H), 7.43 (s, 2H), 6.61 (s, 2H), 5.47-5.40 (m, 1H), 4.13 (s, 3H), 3.81-3.72 (m, 2H), 2.94-2.79 (m, 2H), 2.25-1.88 (m, 17H). LCMS (M+H).sup.+=461.3.

Example A76

(R)-3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-(3-(methoxymethyl)morpholino)phenyl)oxetan-3-ol

[0724] ##STR00348##

Step 1: (R)-4-(3,5-dibromophenyl)-3-(methoxymethyl)morpholine

[0725] ##STR00349##

[0726] The title compound (0.41 g, 370%) was prepared in a manner similar to that in Example A59 step 1 from 1,3-dibromo-5-iodobenzene and (R)-3-(methoxymethyl)morpholine. LCMS (M+H).sup.+=366.

Step 2: (R)-3-(3-bromo-5-(3-(methoxymethyl)morpholino)phenyl)oxetan-3-ol

[0727] ##STR00350##

[0728] The title compound (0.14 g, 35%) was prepared in a manner similar to that in Example A54 step 1 from (R)-4-(3,5-dibromophenyl)-3-(methoxymethyl)morpholine and oxetan-3-one. LCMS (M+H).sup.+=358,360.

Step 3: (R)-3-(3-(3-(methoxymethyl)morpholino)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)oxetan-3-ol

[0729] ##STR00351##

[0730] The title compound (0.14 g, 88%) was prepared in a manner similar to that in Example A1 step 6 from (R)-3-(3-bromo-5-(3-(methoxymethyl)morpholino)phenyl)oxetan-3-ol and BPD. LCMS (M+H).sup.+=406.

Step 4: (R)-3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-(3-(methoxymethyl)morpholino)phenyl)oxetan-3-ol

[0731] Example A76 (45 mg, 21%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and (R)-3-(3-(3-(methoxymethyl)morpholino)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)oxetan-3-ol. .sup.1H NMR (400 MHz, DMSO-d6) ? 8.27 (s, 1H), 8.13 (s, 1H), 7.57 (s, 1H), 7.52 (s, 1H), 7.30 (s, 1H), 7.04 (s, 1H), 6.73 (s, 2H), 6.31 (s, 1H), 4.78-4.69 (m, 4H), 4.15-4.05 (m, 1H), 3.98-3.86 (m, 3H), 3.70-3.53 (m, 3H), 3.32-3.26 (m, 1H), 3.19 (s, 3H), 3.17-3.13 (m, 1H), 3.12-3.03 (m, 1H), 2.91-2.82 (m, 2H), 2.21 (s, 3H), 2.07-1.93 (m, 6H). LCMS (M+H).sup.+=552.2.

Example A77

5-(3,5-dimethyl-4-(2-oxa-6-azaspiro[3.3]heptan-6-yl)phenyl)-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine

[0732] ##STR00352##

Step 1: 6-(4-chloro-2,6-dimethylphenyl)-2-oxa-6-azaspiro[3.3]heptane

[0733] ##STR00353##

[0734] To a solution of 2-bromo-5-chloro-1,3-dimethylbenzene (200 mg, 0.87 mmol) in dioxane (6 mL) was added 2-oxa-6-azaspiro[3.3]heptane (181 mg, 1.73 mmol), Cs.sub.2CO.sub.3 (891 mg, 2.60 mmol), P(t-Bu).sub.3 Palladacycle Gen, 3 (53 mg, 0.09 mmol) and P(t-Bu).sub.3-HBF.sub.4 (27 mg, 0.09 mmol) at room temperature then the mixture was warmed to 90? C. and stirred for 5 h under nitrogen. The mixture was cooled to room temperature and concentrated under vacuum. The residue was purified by silica gel chromatography, eluting with MeOH in DCM (0% to 13% gradient) to give the title compound (163 mg, 79%). LC-MS (M+H).sup.+=238.2.

Step 2: 6-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-2-oxa-6-azaspiro[3.3]heptane

[0735] ##STR00354##

[0736] The title compound (175 mg, 78%) was prepared in a manner similar to that in Example A54 step 1 from 6-(4-chloro-2,6-dimethylphenyl)-2-oxa-6-azaspiro[3.3]heptane. LC-MS (M+H).sup.+=330.0.

Step 3: 5-(3,5-dimethyl-4-(2-oxa-6-azaspiro[3.3]heptan-6-yl)phenyl)-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine

[0737] Example A77 (7 mg, 9%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and 6-(2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-2-oxa-6-azaspiro[3.3]heptane. .sup.1H NMR (400 MHz, DMSO-d.sub.6) ? 8.08 (s, 2H), 7.78 (s, 1H), 7.28 (s, 2H), 6.45 (s, 2H), 4.68 (s, 4H), 4.27 (s, 4H), 4.17-4.07 (m, 1H), 2.91-2.82 (m, 2H), 2.23 (d, J=14.3 Hz, 9H), 2.13-1.91 (m, 6H). LC-MS (M+H).sup.+=476.4.

Example A78

3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-(2-oxa-6-azaspiro[3.3]heptan-6-yl)phenyl)oxetan-3-ol

[0738] ##STR00355##

Step 1: 6-(3-bromo-5-chlorophenyl)-2-oxa-6-azaspiro[3.3]heptane

[0739] ##STR00356##

[0740] The title compound (650 mg, 49%) was prepared in a manner similar to that in Example A22 step 1 from 1-bromo-3-chloro-5-fluorobenzene and 2-oxa-6-azaspiro[3.3]heptane. LC-MS (M+H).sup.+=287.9.

Step 2: 3-(3-chloro-5-(2-oxa-6-azaspiro[3.3]heptan-6-yl)phenyl)oxetan-3-ol

[0741] ##STR00357##

[0742] The title compound (320 mg, 66%) was prepared in a manner similar to that in Example A54 step 1 from 6-(3-bromo-5-chlorophenyl)-2-oxa-6-azaspiro[3.3]heptane and 3-oxetanone. LC-MS (M+H).sup.+=282.0.

Step 3: 3-(3-(2-oxa-6-azaspiro[3.3]heptan-6-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)oxetan-3-ol

[0743] ##STR00358##

[0744] The title compound (134 mg, 51%) was prepared in a manner similar to that in Example A1 step 6 from 3-(3-chloro-5-(2-oxa-6-azaspiro[3.3]heptan-6-yl)phenyl)oxetan-3-ol and BPD. LC-MS (M+H).sup.+=374.1.

Step 4: 3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-(2-oxa-6-azaspiro[3.3]heptan-6-yl)phenyl)oxetan-3-ol

[0745] Example A78 (17 mg, 12%) was prepared in a manner similar to that in Example A1 step 6 from 3-(3-(2-oxa-6-azaspiro[3.3]heptan-6-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)oxetan-3-ol and 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine. .sup.1H NMR (300 MHz, DMSO-d.sub.6) ? 8.21 (s, 1H), 8.14 (s, 1H), 7.56 (s, 1H), 7.43 (s, 1H), 6.82 (s, 1H), 6.69 (s, 2H), 6.55 (s, 1H), 6.27 (s, 1H), 4.77-4.64 (m, 8H), 4.19-4.07 (m, 1H), 4.01 (s, 4H), 2.91-2.82 (m, 2H), 2.20 (s, 3H), 2.11-1.90 (m, 6H). LC-MS (M+H).sup.+=520.4.

Example A79

3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-(tetrahydro-2H-pyran-4-yl)phenyl)oxetan-3-ol

[0746] ##STR00359##

Step 1: 4-(3,5-dibromophenyl)oxan-4-ol

[0747] ##STR00360##

[0748] The title compound (3.2 g, 30;%) was prepared in a manner similar to that in Example A58 step 1 from 1,3,5-tribromobenzene and tetrahydropyran-4-one. .sup.1H NMR (300 MHz, DMSO-d.sub.6) ? 7.70-7.61 (m, 3H), 5.31 (s, 1H), 3.77-3.60 (m, 4H), 2.02-1.82 (m, 2H), 1.52-1.41 (m, 2H).

Step 2: 4-(3,5-dibromophenyl)-tetrahydro-2H-pyran

[0749] ##STR00361##

[0750] A mixture of 4-(3,5-dibromophenyl)oxan-4-ol (300 mg, 0.89 mmol), Et.sub.3SiH (1.56 g, 13.4 mmol) and TFA (1.63 g, 14.3 mmol) in DCM (5 mL) was stirred for overnight at 40? C. under nitrogen. The mixture was cooled to room temperature and concentrated under vacuum. The residue was purified by reverse phase chromatography to give the title compound (100 mg, 28%).

Step 3: 3-(3-bromo-5-(tetrahydro-2H-pyran-4-yl)phenyl)oxetan-3-ol

[0751] ##STR00362##

[0752] The title compound (150 mg, 17%) was prepared in a manner similar to that in Example A54 step 1 from 4-(3,5-dibromophenyl)oxane and 3-oxetanone.

Step 4: 3-(3-(tetrahydro-2H-pyran-4-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)oxetan-3-ol

[0753] ##STR00363##

[0754] The title compound (44 mg, 13%) was prepared in a manner similar to that in Example A1 step 6 from 3-(3-bromo-5-(tetrahydro-2H-pyran-4-yl)phenyl)oxetan-3-ol.

Step 5: 3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-(tetrahydro-2H-pyran-4-yl)phenyl)oxetan-3-ol

[0755] Example A79 (22 mg, 10%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and 3-(3-(tetrahydro-2H-pyran-4-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)oxetan-3-ol. .sup.1H NMR (300 MHz, DMSO-d.sub.6) ? 8.29 (s, 1H), 8.16 (s, 1H), 7.92 (s, 1H), 7.65 (s, 1H), 7.58 (s, 1H), 7.40 (s, 1H), 6.73 (s, 2H), 6.35 (s, 1H), 4.82-4.71 (m, 4H), 4.18-4.04 (m, 1H), 4.02-3.93 (m, 2H), 3.53-3.39 (m, 2H), 2.92-2.76 (m, 3H), 2.22 (s, 3H), 2.11-1.92 (m, 6H), 1.79-1.67 (m, 4H). LC-MS (M+H).sup.+=507.0.

Example A80A/A80B

(R)-3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-((R)-3-methylmorpholino)phenyl)tetrahydrofuran-3-ol & (S)-3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-((R)-3-methylmorpholino)phenyl)tetrahydrofuran-3-ol

[0756] ##STR00364##

Step 1: 3-(3-bromo-5-((R)-3-methylmorpholino)phenyl)tetrahydrofuran-3-ol

[0757] ##STR00365##

[0758] The title compound (500 mg, 48%) was prepared in a manner similar to that in Example A54 step 1 from (3R)-4-(3,5-dibromophenyl)-3-methylmorpholine and dihydrofuran-3-one. LC-MS (M+H).sup.+=341.9.

Step 2: 3-(3-((R)-3-methylmorpholino)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)tetrahydrofuran-3-ol

[0759] ##STR00366##

[0760] The title compound (300 mg, 65%) was prepared in a manner similar to that in Example A1 step 6 from 3-(3-bromo-5-((R)-3-methylmorpholino)phenyl)tetrahydrofuran-3-ol and BPD. LC-MS (M+H).sup.+=390.1.

Step 3: (R)-3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-((R)-3-methylmorpholino)phenyl)tetrahydrofuran-3-ol & (S)-3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-((R)-3-methylmorpholino)phenyl)tetrahydrofuran-3-ol

[0761] Examples A80A/A80B were prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and 3-(3-((R)-3-methylmorpholino)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)tetrahydrofuran-3-ol, then the isomers were separated by chiral-HPLC. Analytical chiral-HPLC condition: CHIRALPAK IA3, 4.6?50 mm, 3 ?m; (Hexane:DCM=3:1, contains 0.1% Et.sub.2NH):IPA=4:1; 1 mL/min; 25? C.

Example A80A

[0762] ((S)-3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-((R)-3-methylmorpholino)phenyl)tetrahydrofuran-3-ol): (22 mg, 35%) .sup.1H NMR (300 MHz, DMSO-d.sub.6) ? 8.25 (s, 1H), 8.12 (s, 1H), 7.58 (s, 1H), 7.39 (s, 1H), 7.22 (s, 1H), 6.99 (s, 1H), 6.69 (s, 2H), 5.35 (s, 1H), 4.18-3.51 (m, 10H), 3.26-3.16 (m, 1H), 3.13-2.98 (m, 1H), 2.92-2.82 (m, 2H), 2.39-2.24 (m, 1H), 2.22 (s, 3H), 2.17-1.88 (m, 7H), 1.00 (d, J=6.4 Hz, 3H). LC-MS (M+H).sup.+=536.4. Chiral HPLC: tR=1.55 min.

Example A80B

[0763] ((R)-3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-((R)-3-methylmorpholino)phenyl)tetrahydrofuran-3-ol): (23 mg, 39%) .sup.1H NMR (300 MHz, DMSO-d.sub.6) ? 8.25 (s, 1H), 8.12 (s, 1H), 7.58 (s, 1H), 7.39 (s, 1H), 7.22 (s, 1H), 6.99 (s, 1H), 6.69 (s, 2H), 5.35 (s, 1H), 4.18-3.51 (m, 10H), 3.26-3.16 (m, 1H), 3.13-2.98 (m, 1H), 2.92-2.82 (m, 2H), 2.39-2.24 (m, 1H), 2.22 (s, 3H), 2.17-1.88 (m, 7H), 1.00 (d, J=6.4 Hz, 3H). LC-MS (M+H).sup.+=536.4. Chiral HPLC: tR=2.57 min.

Example A81

3-(5-(5-amino-6-(1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-3-methyl-2-(prop-1-yn-1-yl)phenyl)oxetan-3-ol

[0764] ##STR00367##

Step 1: 1-bromo-5-chloro-2-iodo-3-methylbenzene

[0765] ##STR00368##

[0766] A suspension of 2-bromo-4-chloro-6-methylaniline (5.0 g, 22.8 mmol) in water (40 mL) and conc. HCl (30 mL) was cooled to ?5? C. To the above suspension was added an aqueous solution of NaNO.sub.2 (1.73 g, 25.1 mmol) dropwise while keeping the temperature below 0? C. After 30 min, the mixture was added slowly into KI (4.54 g, 27.4 mmol) in 300 mL ice water with vigorous stirring. The mixture was stirred overnight at room temperature. The mixture was extracted with of EtOAc (400 mL?2). The combined organic layer was washed with NaHSO.sub.3, dried over Na.sub.2SO.sub.4, filtered and concentrated. The residue was purified by silica gel chromatograph with PE to give the title compound (4.5 g, 60%).

Step 2: 1-bromo-5-chloro-3-methyl-2-(prop-1-yn-1-yl)benzene

[0767] ##STR00369##

[0768] To a solution of 1-bromo-5-chloro-2-iodo-3-methylbenzene (2.0 g, 6.1 mmol) in toluene (30 mL) was added trimethyl(prop-1-yn-1-yl)silane (680 mg, 6.1 mmol), triethylamine (1.85 g, 18.3 mmol), CuI (348 mg, 1.8 mmol), Pd(PPh.sub.3).sub.4 (352 mg, 0.3 mmol) and TBAF (1.6 g, 6.1 mmol). The mixture was stirred for overnight at room temperature under nitrogen. EtOAc (100 mL) was added and the organic phase was successively washed with H.sub.2O (50 mL), brine (50 mL), dried over Na.sub.2SO.sub.4, filtered and concentrated under vacuum. The residue was purified by silica gel chromatograph with PE to give the title compound (1.2 g, 82%). .sup.1H NMR (400 MHz, DMSO-d6) ? 7.64 (s, 1H), 7.43 (s, 1H), 2.40 (s, 3H), 2.15 (s, 3H).

Step 3: 3-(5-chloro-3-methyl-2-(prop-1-yn-1-yl)phenyl)oxetan-3-ol

[0769] ##STR00370##

[0770] To a solution of 1-bromo-5-chloro-3-methyl-2-(prop-1-yn-1-yl)benzene (1.2 g, 5.0 mmol) in THF (10 mL) was added n-BuLi (2.5 M in hexane, 2 mL) at ?78? C. dropwise under nitrogen. After 40 min, oxetan-3-one (357 mg, 5.0 mmol) was added dropwise at ?78? C. and the mixture was stirred for another 2 h. The mixture was quenched by saturated NH.sub.4Cl (30 mL), warmed to room temperature, diluted with EtOAc (40 mL) and washed with brine (15 mL?2). The organic layer was dried over Na.sub.2SO.sub.4, filtered and concentrated. The residue was purified by silica gel chromatograph, with PE:EtOAc=14:5 to give the title compound (770 mg, 66%). LC-MS (M+H).sup.+=237.2.

Step 4: 3-(3-methyl-2-(prop-1-yn-1-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)oxetan-3-ol

[0771] ##STR00371##

[0772] To a solution of 3-(5-chloro-3-methyl-2-(prop-1-yn-1-yl)phenyl)oxetan-3-ol (300 mg, 1.3 mmol) in dioxane (10 mL) was added BPD (645 mg, 2.6 mmol), KOAc (250 mg, 2.5 mmol), Pd.sub.2(dba).sub.3 (116 mg, 0.13 mmol) and XPhos (121 mg, 0.25 mmol). The mixture was stirred for overnight at 110? C. under nitrogen. The mixture was cooled to room temperature, diluted with EtOAc (40 mL), then successively washed with H.sub.2O (15 mL) and brine (15 mL). The organic layer was dried over Na.sub.2SO.sub.4, filtered and concentrated. The residue was purified by silica gel chromatograph with PE:EtOAc=1:1 to give the title compound (360 mg, 86%). LC-MS (M+H).sup.+=329.3.

Step 5: 3-(5-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-3-methyl-2-(prop-1-yn-1-yl)phenyl)oxetan-3-ol

[0773] To a solution of 3-(3-methyl-2-(prop-1-yn-1-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)oxetan-3-ol (300 mg, 0.91 mmol) in dioxane (10 mL) and water (1 mL) was added 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine (322 mg, 0.91 mmol), K.sub.2CO.sub.3 (628 mg, 4.6 mmol) and Pd(dppf)Cl.sub.2.Math.DCM (74 mg, 0.09 mmol), then the mixture was warmed to at 100? C. under nitrogen. After 1 h, the mixture cooled to room temperature, diluted with EtOAc (30 mL), then successively washed with H.sub.2O (15 mL) and brine (15 mL). The organic layer was dried over Na.sub.2SO.sub.4, filtered and concentrated. The residue was purified by silica gel prep-TLC, developing with MeOH:DCM=1:4, then further purified by prep-HPLC to give Example A81 (6 mg, 14%), 1H NMR (400 MHz, DMSO-d6) ? 8.31 (s, 1H), 8.10 (s, 1H), 7.70 (s, 1H), 7.58 (s, 1H), 7.55 (s, 1H), 6.81 (s, 2H), 6.04 (s, 1H), 5.11 (d, J=6.9 Hz, 2H), 4.68 (d, J=6.9 Hz, 2H), 4.17-4.06 (m, 1H), 2.90-2.83 (m, 2H), 2.38 (s, 3H), 2.21 (s, 3H), 2.09 (s, 3H), 2.06-1.94 (m, 6H). LC-MS (M+H).sup.+=475.4.

Example A82

3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-(methoxymethyl)phenyl)oxetan-3-ol

[0774] ##STR00372##

Step 1: (3,5-dibromophenyl methanol

[0775] ##STR00373##

[0776] To a solution of 3,5-dibromobenzoic acid (2.0 g, 7.1 mmol) in THF (20 mL) was added BH.sub.3 in THF (1.0 M, 14 mL, 14 mmol). The mixture was stirred at room temperature for overnight, then methanol (10 mL) was carefully added. The mixture was concentrated under reduced pressure, and the residue was purified by silica gel chromatograph (PE:EtOAc=5:1) to give the title compound (1.8 g, 95%). LC-MS (M+H).sup.+=265.8, 267.8.

Step 2: 1,3-dibromo-5-(methoxymethyl)benzene

[0777] ##STR00374##

[0778] To a solution of (3,5-dibromophenyl)methanol (1.8 g, 6.7 mmol) in THF (20 mL) was added NaH (60%, 330 mg, 8.25 mmol) at room temperature. After 1 h, Mel (0.70 mL, 11.2 mmol) was added. The mixture was stirred at room temperature for overnight. Saturated NH.sub.4C.sub.1 (10 mL) and water (10 mL) was added. The mixture was extracted with EtOAc (40 mL?2). The combined organic layer was washed with brine (50 mL?3), dried over Na.sub.2SO.sub.4, filtered and concentrated under vacuum. The residue was purified by silica gel chromatograph (PE:EtOAc=5:1) to give the title compound (1.5 g, 78%). LC-MS (M+H).sup.+=278.9, 280.9.

Step 3: 3-(3-bromo-5-(methoxymethyl)phenyl)oxetan-3-ol

[0779] ##STR00375##

[0780] The title compound (550 mg, 34%) was prepared in a manner similar to that in Example A54 step 1 from 1,3-dibromo-5-(methoxymethyl)benzene and oxetan-3-one. LC-MS (M+H).sup.+=273.0, 275.0.

Step 4: 3-(3-(methoxymethyl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)oxetan-3-ol

[0781] ##STR00376##

[0782] The title compound (500 mg, 77%) was prepared in a manner similar to that in Example A1 step 6 from 3-(3-bromo-5-(methoxymethyl)phenyl)oxetan-3-ol and BPD. LC-MS (M+H).sup.+=321.2.

Step 5: 3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-(methoxymethyl)phenyl)oxetan-3-ol

[0783] Example A82 (20 mg, 15%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and 3-(3-(methoxymethyl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)oxetan-3-ol. .sup.1H NMR (400 MHz, DMSO-d6) ? 8.28 (s, 1H), 8.15 (s, 1H), 8.01 (s, 1H), 7.72 (s, 1H), 7.59 (s, 1H), 7.47 (s, 1H), 6.78 (s, 2H), 6.42 (s, 1H), 4.79-4.71 (m, 4H), 4.47 (s, 2H), 4.11-4.08 (m, 1H), 3.32 (s, 3H), 2.88-2.85 (m, 2H), 2.21 (s, 3H), 2.0-1.9 (m, 6H). LC-MS (M+H).sup.+=467.2.

Example A83

3-(5-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-3-methyl-2-(2-oxa-6-azaspiro[3.3]heptan-6-yl)phenyl)tetrahydrofuran-3-ol

[0784] ##STR00377##

Step 1: 3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazin-2-amine

[0785] ##STR00378##

[0786] A mixture of 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine (2.0 g, 5.66 mmol) and BPD (2.88 g, 11.3 mmol) and Pd.sub.2(dba).sub.3 (0.26 g, 0.283 mmol) and tricyclohexylphosphine (0.12 g, 0.425 mmol) and KOAc (1.11 g, 11.3 mmol) in dioxane (20 mL) was stirred for overnight at 110? C. under nitrogen. The mixture was cooled to room temperature and concentrated under reduced pressure. The residue was purified by reverse phase chromatography with acetonitrile/water to give the title compound (1.5 g, 66%). .sup.1H NMR (400 MHz, DMSO-d.sub.6) ? 8.01 (s, 1H), 7.90 (s, 1H), 7.56 (s, 1H), 6.97 (s, 2H), 4.15-4.03 (m, 1H), 2.87-2.78 (m, 4H), 2.20 (s, 3H), 2.08-1.79 (m, 4H), 1.16 (s, 12H). LC-MS (M?pin+H).sup.+=319.0.

Step 2: 6-(2-bromo-4-chloro-6-methylphenyl)-2-oxa-6-azaspiro[3.3]heptane

[0787] ##STR00379##

[0788] To a solution of 1-bromo-5-chloro-2-iodo-3-methylbenzene (2.0 g, 5.5 mmol) in dioxane (20 mL) and 2-oxa-6-azaspiro[3.3]heptane (630 mg, 6.04 mmol) was added Cs.sub.2CO.sub.3 (2.83 g, 8.24 mmol), Pd.sub.2(dba).sub.3 (159 mg, 0.17 mmol), and XantPhos (201 mg, 0.33 mmol) under nitrogen then the mixture was warmed to 90? C. After 16 h, the mixture was cooled to room temperature and concentrated under reduced pressure. The residue was purified by silica gel chromatography, eluting with EtOAc in PE (0% to 30% gradient) to give the title compound (1.52 g, 91%). LC-MS (M+1).sup.+=301.9.

Step 3: 3-(5-chloro-3-methyl-2-(2-oxa-6-azaspiro[3.3]heptan-6-yl)phenyl)tetrahydrofuran-3-ol

[0789] ##STR00380##

[0790] The title compound (150 mg, 37%) was prepared in a manner similar to that in Example A54 step 1 from 6-(2-bromo-4-chloro-6-methylphenyl)-2-oxa-6-azaspiro[3.3]heptane and dihydrofuran-3-one. LC-MS (M+1).sup.+=310.0.

Step 4: 3-(5-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-3-methyl-2-(2-oxa-6-azaspiro[3.3]heptan-6-yl)phenyl)tetrahydrofuran-3-ol

[0791] To a solution of 3-(5-chloro-3-methyl-2-(2-oxa-6-azaspiro[3.3]heptan-6-yl)phenyl)tetrahydrofuran-3-ol (100 mg, 0.31 mmol) in dioxane (2 mL) and H.sub.2O (0.20 mL) was added 3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazin-2-amine (230 mg, 0.57 mmol), K.sub.2CO.sub.3 (89 mg, 0.62 mmol) and dichlorobis(tricyclohexylphosphine)palladium(II) (24 mg, 0.03 mmol) under nitrogen. The mixture was warmed to 100? C. and stirred for 2 h. The mixture was cooled to room temperature and diluted with water (30 mL). The mixture was extracted with DCM (30 mL?3). The combined organic layers were washed with brine (30 mL), dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure. The residue was purified by prep-HPLC to give Example A83 (25 mg, 15%) obtained. .sup.1H NMR (300 MHz, DMSO-d6) ? 8.22 (s, 1H), 8.12 (s, 1H), 7.76 (s, 1H), 7.59 (s, 2H), 6.72 (s, 2H), 5.93 (s, 1H), 4.82-4.76 (m, 4H), 4.21-3.96 (m, 7H), 3.94-3.85 (m, 1H), 3.76 (d, J=8.9 Hz, 1H), 2.92-2.83 (m, 2H), 2.41 (s, 3H), 2.37-2.25 (m, 1H), 2.22 (s, 3H), 2.20-2.14 (m, 1H), 2.08-1.97 (m, 6H). LC-MS (M+H).sup.+=548.4.

Example A84

3-(5-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2-chloro-3-methylphenyl)oxetan-3-ol

[0792] ##STR00381##

Step 1: 1-bromo-2,5-dichloro-3-methylbenzene

[0793] ##STR00382##

[0794] To a solution of 2-bromo-4-chloro-6-methylaniline (1.5 g, 6.46 mmol) in acetonitrile (10 mL) was added t-BuNO.sub.2 (1.05 g, 9.7 mmol) and CuCl.sub.2 (1.10 g, 7.8 mmol) under nitrogen. The mixture was warmed to 60? C. and stirred for 15 h. The mixture was cooled to room temperature jo and concentrated under vacuum. The residue was purified by silica gel chromatography, eluting with DCM in PE (0% to 10% gradient) to give the title compound (1.36 g, 88%). .sup.1H NMR (400 MHz, DMSO-d6) ? 7.78 (s, 1H), 7.55 (s, 1H), 2.44 (s, 3H).

Step 2: 3-(2,5-dichloro-3-methylphenyl)oxetan-3-ol

[0795] ##STR00383##

[0796] The title compound (159 mg, 48%) was prepared in a manner similar to that in Example A54 step 1 from 1-bromo-2,5-dichloro-3-methylbenzene and 3-oxetanone. LC-MS (M+H).sup.+=233.0.

Step 3: 3-(2-chloro-3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)oxetan-3-ol

[0797] ##STR00384##

[0798] The title compound (125 mg, 63%) was prepared in a manner similar to that in Example A54 step 2 from 3-(2,5-dichloro-3-methylphenyl)oxetan-3-ol and BPD. LC-MS (M+H).sup.+=325.0.

Step 4: 3-(5-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2-chloro-3-methylphenyl)oxetan-3-ol

[0799] ##STR00385##

[0800] Example A84 (19 mg, 18/o) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and 3-(2-chloro-3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)oxetan-3-ol. .sup.1H NMR (400 MHz, DMSO-d.sub.6) ? 8.34 (s, 1H), 8.10 (s, 1H), 7.81 (s, 1H), 7.65-7.57 (m, 2H), 6.81 (s, 2H), 6.23 (s, 1H), 5.08 (d, J=7.1 Hz, 2H), 4.71 (d, J=7.0 Hz, 2H), 4.18-4.05 (m, 1H), 2.91-2.83 (m, 2H), 2.37 (s, 3H), 2.21 (s, 3H), 2.10-1.95 (m, 6H). LC-MS (M+H).sup.+=471.3.

Example A85

(S)-3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-(2-(hydroxymethyl)pyrrolidin-1-yl)phenyl)oxetan-3-ol

[0801] ##STR00386##

Step 1: (S)-(1-(3,5-dibromophenyl)pyrrolidin-2-yl)methanol

[0802] ##STR00387##

[0803] The title compound (1.87 g, 20%) was prepared in a manner similar to that in A59 step 1 from 1,3-dibromo-5-iodobenzene and (S)-prolinol. LC-MS (M+H).sup.+=335.8.

Step 2: (S)-2-(((tert-butyldimethylsilyl)oxy)methyl)-1-(3,5-dibromophenyl)pyrrolidine

[0804] ##STR00388##

[0805] To a stirred solution of (S)-(1-(3,5-dibromophenyl)pyrrolidin-2-yl)methanol (1.0 g, 3.0 mmol) in DMF (10 mL) was added TBSCl (0.90 g, 6.0 mmol) and imidazole (0.41 g, 6.0 mmol) at room temperature. The mixture was stirred for 16 h at 50? C. under nitrogen. The mixture was cooled to room temperature and poured into water (30 mL), then successively extracted with DCM (30 mL?2). The combined organic layer was washed with brine, dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure. The residue was purified by flash chromatography, eluting with EtOAc in PE (0% to 20% gradient) to give the title compound (787 mg, 59%). LC-MS (M+H).sup.+=449.1.

Step 3: (S)-3-(3-bromo-5-(2-(((tert-butyldimethylsilyl)oxy)methyl)pyrrolidin-1-yl)phenyl)oxetan-3-ol

[0806] ##STR00389##

[0807] The title compound (292 mg, 42%) was prepared in a manner similar to that in Example A54 step 1 from (S)-2-(((tert-butyldimethylsilyl)oxy)methyl)-1-(3,5-dibromophenyl)pyrrolidine and 3-oxetanone. LC-MS (M+H).sup.+=443.9.

Step 4: (S)-3-(3-(2-(((tert-butyldimethylsilyl)oxy)methyl)pyrrolidin-1-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)oxetan-3-ol

[0808] ##STR00390##

[0809] The title compound (127 mg, 58%) was prepared in a manner similar to that in Example A1 step 6 from 3(S)-3-(3-bromo-5-(2-(((tert-butyldimethylsilyl)oxy)methyl)pyrrolidin-1-yl)phenyl)oxetan-3-ol and BPD. LC-MS (M+H).sup.+=490.2.

Step 5: (S)-3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-(2-(((tert-butyldimethylsilyl)oxy)methyl)pyrrolidin-1-yl)phenyl)oxetan-3-ol

[0810] ##STR00391##

[0811] The title compound (117 mg, 900%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and (S)-3-(3-(2-(((tert-butyldimethylsilyl)oxy)methyl)pyrrolidin-1-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)oxetan-3-ol. LC-MS (M+H).sup.+=636.4.

Step 6: 3(S)-3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-(2-(hydroxymethyl)pyrrolidin-1-yl)phenyl)oxetan-3-ol

[0812] To a stirred solution of (S)-3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-(2-(((tert-butyldimethylsilyl)oxy)methyl)pyrrolidin-1-yl)phenyl)oxetan-3-ol (100 mg, 0.157 mmol) in THF (5 mL) was added TBAF (82.3 mg, 0.314 mmol) at room temperature and kept for 1 h under nitrogen. The mixture was concentrated under reduced pressure. The residue was purified by prep-HPLC to give Example A85 (31 mg, 37%). .sup.1H NMR (400 MHz, jo DMSO-d.sub.6) ? 8.22 (s, 1H), 8.13 (s, 1H), 7.60 (s, 1H), 7.33 (s, 1H), 6.99 (s, 1H), 6.76 (s, 1H), 6.66 (s, 2H), 6.23 (s, 1H), 4.81 (s, 1H), 4.76-4.72 (m, 4H), 4.17-4.04 (m, 1H), 3.81-3.72 (m, 1H), 3.58-3.50 (m, 1H), 3.48-3.39 (m, 1H), 3.26-3.16 (m, 1H), 3.16-3.06 (m, 1H), 2.90-2.81 (m, 2H), 2.21 (s, 3H), 2.10-1.83 (m, 10H). LC-MS (M+H).sup.+=522.4.

Example A86

3-(5-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2-(3,6-dihydro-2H-pyran-4-yl)-3-methylphenyl)oxetan-3-ol

[0813] ##STR00392##

Step 1: 4-(2-bromo-4-chloro-6-methylphenyl)-3,6-dihydro-2H-pyran

[0814] ##STR00393##

[0815] The title compound (446 mg, 56%) was prepared in a manner similar to that in Example A75 step 1 from 1-bromo-5-chloro-2-iodo-3-methylbenzene and 2-(3,6-dihydro-2H-pyran-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane. .sup.1H NMR (400 MHz, DMSO-d.sub.6) ? 7.59 (s, 1H), 7.38 (s, 1H), 5.60 (s, 1H), 4.27-4.11 (m, 2H), 3.91-3.75 (m, 2H), 2.62-2.58 (m, 2H), 2.27 (s, 3H).

Step 2: 3-(5-chloro-2-(3,6-dihydro-2H-pyran-yl-3-methylphenyl)oxetan-3-ol

[0816] ##STR00394##

[0817] The title compound (286 mg, 66%) was prepared in a manner similar to that in Example A54 step 1 from 4-(2-bromo-4-chloro-6-methylphenyl)-3,6-dihydro-2H-pyran and 3-oxetanone. .sup.1H NMR (300 MHz, DMSO-d.sub.6) ? 7.27 (s, 1H), 7.02 (s, 1H), 6.20 (s, 1H), 5.59 (s, 1H), 5.05 (d, J=7.1 Hz, 1H), 4.91 (d, J=6.9 Hz, 1H), 4.55-4.45 (m, 2H), 4.23-4.03 (m, 2H), 3.87-3.66 (m, 2H), 2.55-2.46 (m, 2H), 2.21 (s, 3H).

Step 3: 3-(2-(3,6-dihydro-2H-pyran-4-yl)-3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)oxetan-3-ol

[0818] ##STR00395##

[0819] The title compound (369 mg, 97%) was prepared in a manner similar to that in Example A54 step 2 from 3-(5-chloro-2-(3,6-dihydro-2H-pyran-4-yl)-3-methylphenyl)oxetan-3-ol and BPD. LC-MS (M?H.sub.2O+H).sup.+=355.2.

Step 4: 3-(5-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2-(3,6-dihydro-2H-pyran-4-yl)-3-methylphenyl)oxetan-3-ol

[0820] Example A86 (20 mg, 49%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and 3-(2-(3,6-dihydro-2H-pyran-4-yl)-3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)oxetan-3-ol. .sup.1H NMR (30) MHz, DMSO-4) ? 8.26 (s, 1H), 8.10 (s, 1H), 7.64 (s, 1H), 7.60 (s, 1H), 7.43 (s, 1H), 6.72 (s, 2H), 6.10 (s, 1H), 5.59 (s, 1H), 5.11 (d, J=6.9 Hz, 1H), 4.96 (d, J=6.7 Hz, 1H), 4.54 (t, J=6.3 Hz, 2H), 4.21-4.05 (s, 3H), 3.87-3.70 (m, 2H), 2.92-2.82 (m, 2H), 2.43-2.29 (m, 2H), 2.27-2.17 (m, 6H), 2.11-1.92 ((m, 6H). LC-MS (M+H).sup.+=519.4.

Example A87

3-(5-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2-(1,3-dioxolan-2-yl)-3-methylphenyl)oxetan-3-ol

[0821] ##STR00396##

Step 1: 2-bromo-4-chloro-6-methylbenzaldehyde

[0822] ##STR00397##

[0823] To a solution of 4-chloro-2-methylbenzaldehyde (14 g, 86 mmol) in DCE (280 mL) was added NBS(N-bromosuccinimide) (19.3 g, 103 mmol), TFA (56.0 mL, 757 mmol), 4-chloro-2-(trifluoromethyl)aniline (3.54 g, 17.2 mmol), and Pd(OAc).sub.2 (2.03 g, 8.60 mmol) at room temperature. The mixture was stirred for overnight at 60? C. under nitrogen. The mixture was cooled to room temperature and concentrated under reduced pressure. The residue was purified by flash chromatography, eluting with DCM in PE (0% to 25% gradient) to give the title compound (17 g, 85%), 1H NMR (300 MHz, DMSO-d6) ? 10.30 (s, 1H), 7.79 (s, 1H), 7.51 (s, 1H), 2.50 (s, 3H).

Step 2: 2-(2-bromo-4-chloro-6-methylphenyl)-1,3-dioxolane

[0824] ##STR00398##

[0825] To a stirred solution of 2-bromo-4-chloro-6-methylbenzaldehyde (14.0 g, 59.9 mmol) in toluene (500 mL) was added TsOH (2.17 g, 12.0 mmol) and ethylene glycol (5.87 g, 89.9 mmol) at room temperature. The mixture was stirred for overnight at 120? C. under a Dean-Stark receiver. The mixture was cooled to room temperature and concentrated under reduced pressure. The residue was purified by flash chromatography eluting with DCM in PE (0% to 40% gradient) to give the title compound (13.0 g, 79%). .sup.1H NMR (400 MHz, DMSO-d6) ? 7.62 (s, 1H), 7.37 (s, 1H), 6.13 (s, 1H), 4.22-3.93 (m, 4H).

Step 3: 3-(5-chloro-2-(1,3-dioxolan-2-yl)-3-methylphenyl)oxetan-3-ol

[0826] ##STR00399##

[0827] The title compound (9.45 g, 77%) was prepared in a manner similar to that in Example A54 step 1 from 2-(2-bromo-4-chloro-6-methylphenyl)-1,3-dioxolane and 3-oxetanone. .sup.1H NMR (300 MHz, DMSO-d.sub.6) ? 7.28 (s, 1H), 7.18 (s, 1H), 6.49 (s, 1H), 5.52 (s, 1H), 4.99 (d, J=6.9 Hz, 2H), 4.68 (d, J=6.7 Hz, 2H), 4.15-4.08 (m, 2H), 3.95-3.88 (m, 2H), 2.38 (s, 3H). LC-MS (M+H).sup.+=271.0.

Step 4: 3-(2-(1,3-dioxolan-2-yl)-3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)oxetan-3-ol

[0828] ##STR00400##

[0829] The title compound (240 mg, 95%) was prepared in a manner similar to that in Example A54 step 2 from 3-(5-chloro-2-(1,3-dioxolan-2-yl)-3-methylphenyl)oxetan-3-ol and BPD. LC-MS (M+H).sup.+=363.2.

Step 5: 3-(5-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2-(1,3-dioxolan-2-yl)-3-methylphenyl)oxetan-3-ol

[0830] Example A87 (33 mg, 30%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and 3-(2-(1,3-dioxolan-2-yl)-3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)oxetan-3-ol. .sup.1H NMR (300 MHz, DMSO-d.sub.6) ? 8.34 (s, 1H), 8.11 (s, 1H), 7.65 (s, 1H), 7.60 (s, 1H), 7.54 (s, 1H), 6.80 (s, 2H), 6.38 (s, 1H), 5.56 (s, 1H), 5.07-4.98 (m, 2H), 4.75-4.67 (m, 2H), 4.20-4.07 (m, 3H), 3.94-3.88 (m, 2H), 2.92-2.82 (m, 2H), 2.41 (s, 3H), 2.21 (s, 3H), 2.13-1.92 (m, 6H). LC-MS (M+H).sup.+=509.3.

Example A88

3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylphenyl)tetrahydro-2H-pyran-3-ol

[0831] ##STR00401##

Step 1: 3-(3-bromo-5-methylphenyl)tetrahydro-2H-pyran-3-ol

[0832] ##STR00402##

[0833] The title compound (1.8 g, 83%) was prepared in a manner similar to that in Example A54 step 1 from 1,3-dibromo-5-methylbenzene and dihydro-2H-pyran-3(4H)-one. LCMS (M-OH).sup.+=253, 255.

Step 2: 3-(3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)tetrahydro-2H-pyran-3-ol

[0834] ##STR00403##

[0835] The title compound (2.0 g, 94%) was prepared in a manner similar to that in Example A1 step 6 from 3-(3-bromo-5-methylphenyl)tetrahydro-2H-pyran-3-ol and BPD. LCMS (M?OH).sup.+=301.

Step 3: 3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-methylphenyl)tetrahydro-2H-pyran-3-ol

[0836] Example A88 (165 mg, 84%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and 3-(3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)tetrahydro-2H-pyran-3-ol. .sup.1H NMR (400 MHz, DMSO-d6) ? 8.24 (s, 1H), 8.21 (s, 1H), 7.86 (s, 1H), 7.58 (s, 1H), 7.54 (s, 1H), 7.27 (s, 1H), 6.71 (s, 2H), 5.26 (s, 1H), 4.20-4.05 (m, 1H), 3.88-3.74 (m, 1H), 3.64-3.58 (m, 1H), 3.56-3.38 (m, 2H), 2.94-2.81 (m, 2H), 2.34 (s, 3H), 2.22 (s, 3H), 2.11-1.96 (m, 8H), 1.77-1.67 (m, 1H), 1.48-1.37 (m, 1H). LCMS (M+H).sup.+=465.5.

Example A89

3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-((R)-3-methylmorpholino)phenyl)tetrahydro-2H-pyran-3-ol

[0837] ##STR00404##

Step 1: 3-(3-bromo-5-((R)-3-methylmorpholino)phenyl)tetrahydro-2H-pyran-3-ol

[0838] ##STR00405##

[0839] To a solution of (R)-4-(3,5-dibromophenyl)-3-methy morpholine (900 mg, 2.70 mmol) in THF (20 mL) was added n-BuLi (2.5 M in hexane, 1.08 mL) dropwise at ?78? C. under nitrogen, then stirred for 30 min at ?78? C. dihydro-2H-pyran-3(4H)-one (405 mg, 4.05 mmol) was added dropwise at this temperature and stirred for another 2 h. The mixture was quenched by saturated NH.sub.4Cl (30 mL), warmed to room temperature, and extracted with EtOAc (100 mL). The organic layer was successively washed with water (100 mL) and brine (100 mL), dried over Na.sub.2SO.sub.4, filtered and concentrated under vacuum. The residue was purified by prep-TLC with PE:EtOAc=1:3 to give the title compound (800 mg, 83%). LC-MS (M+H).sup.+=356.2, 358.3.

Step 2: 3-(3-((R)-3-methylmorpholino)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)tetrahydro-2H-pyran-3-ol

[0840] ##STR00406##

[0841] To a solution of 3-(3-bromo-5-((R)-3-methylmorpholino)phenyl)tetrahydro-2H-pyran-3-ol (800 mg, 2.25 mmol) in dioxane (15 mL) was added BPD (744 mg, 2.93 mmol), KOAc (331 mg, 3.37 mmol) and Pd(dppf)Cl.sub.2.Math.CH.sub.2Cl.sub.2 (184 mg, 0.22 mmol). The mixture was stirred for overnight at 100? C. under nitrogen. The mixture was cooled to room temperature, diluted with EtOAc (50 mL), successively washed with water (50 mL), brine (50 mL), dried over Na.sub.2SO.sub.4, filtered and concentrated under vacuum. The residue was purified by prep-TLC with EtOAc to give the title compound (684 mg, 75%). LC-MS (M+H).sup.+=404.2.

Step 3: 3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-((R)-3-methylmorpholino)phenyl)tetrahydro-2H-pyran-3-ol

[0842] To a solution of 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine (300 mg, 0.85 mmol) in dioxane (10 mL) and water (1 mL) were added 3-(3-((R)-3-methylmorpholino)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)tetrahydro-2H-pyran-3-ol (684 mg, 1.69 mmol), K.sub.2CO.sub.3 (351 mg, 2.55 mmol) and Pd(dppf)Cl.sub.2CH.sub.2Cl.sub.2 (69 mg, 0.08 mmol), then stirred for 5 h at 100? C. under nitrogen. The mixture was cooled to room temperature, diluted with EtOAc (50 mL), successively washed with water (50 mL), brine (50 mL), dried over Na.sub.2SO.sub.4, filtered and concentrated under vacuum. The residue was purified by prep-TLC with MeOH:DCM=1:7, followed by prep-HPLC to give the title compound (190 mg, 41%). .sup.1H NMR (400 MHz, DMSO-d6) ? 8.24 (s, 1H), 8.17 (s, 1H), 7.57 (s, 1H), 7.47 (s, 1H), 7.21 (s, 1H), 7.02 (s, 1H), 6.69 (s, 2H), 5.17 (s, 1H), 4.15-4.05 (m, 1H), 3.94-3.85 (m, 2H), 3.83-3.70 (m, 2H), 3.68-3.40 (m, 5H), 3.26-3.13 (m, 1H), 3.13-2.91 (m, 1H), 2.93-2.79 (m, 2H), 2.22 (s, 3H), 2.14-1.90 (m, 8H), 1.79-1.65 (m, 1H), 1.51-1.38 (m, 1H), 1.03-0.94 (m, 3H). LC-MS (M+H).sup.+=550.2.

Example 90A/90B

(S)-3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-((R)-3-methylmorpholino)phenyl)tetrahydro-2H-pyran-3-ol & (R)-3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-((R)-3-methylmorpholino)phenyl)tetrahydro-2H-pyran-3-ol

[0843] ##STR00407##

[0844] Examples A90A/A90B were prepared by chiral-HPLC separation of 3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-((R)-3-methylmorpholino)phenyl)tetrahydro-2H-pyran-3-ol (97 mg). Analytical chiral-HPLC condition: CHIRALPAK 1H3, 4.6?50 mm, 3 ?m; (MTBE, contains 0.1% Et.sub.2NH):EtOH=9:1; 1 mL/min; 25? C.

[0845] Example A90A: (38 mg, 39%) .sup.1H NMR (400 MHz, DMSO6) ? 8.24 (s, 1H), 8.17 (s, 1H), 7.57 (s, 1H), 7.47 (s, 1H), 7.21 (s, 1H), 7.02 (s, 1H), 6.68 (s, 2H), 5.16 (s, 1H), 4.20-4.04 (m, 1H), 3.94-3.85 (m, 2H), 3.83-3.70 (m, 2H), 3.68-3.40 (m, 5H), 3.25-3.16 (m, 1H), 3.10-2.99 (m, 1H), 2.93-2.79 (m, 2H), 2.23 (s, 3H), 2.13-1.93 (m, 8H), 1.75-1.65 (m, 1H), 1.51-1.38 (m, 1H), 1.03-0.94 (m, 3H). LC-MS (M+H).sup.+=550.2. Chiral HPLC: tR=1.28 min.

[0846] Example A90B: (45.2 mg, 46%).sup.1H NMR (400 MHz, DMSO-d6) ? 8.24 (s, 1H), 8.17 (s, 1H), 7.57 (s, 1H), 7.47 (s, 1H), 7.21 (s, 1H), 7.02 (s, 1H), 6.69 (s, 2H), 5.17 (s, 1H), 4.15-4.05 (m, 1H), 3.94-3.85 (m, 2H), 3.83-3.70 (m, 2H), 3.68-3.40 (m, 5H), 3.26-3.13 (m, 1H), 3.09-2.98 (m, 1H), 2.93-2.79 (m, 2H), 2.22 (s, 3H), 2.14-1.90 (m, 8H), 1.79-1.69 (m, 1H), 1.48-1.38 (m, 1H), 1.03-0.94 (m, 3H). LC-MS (M+H).sup.+=550.4. Chiral HPLC: tR=1.73 min.

Example A91

1-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-(3-hydroxyoxetan-3-yl)phenyl)pyrrolidin-2-one

[0847] ##STR00408##

Step 1: 1-(3,5-dibromophenyl)-2,5-dimethyl-1H-pyrrole

[0848] ##STR00409##

[0849] To a solution of 3,5-dibromoaniline (5.0 g, 20 mmol), hexane-2,5-dione (2.5 g, 22 mmol) and TsOH (68.8 mg, 0.4 mmol) in toluene (30 mL) was heated to reflux under Dean-Stark receiver for 3 h. The mixture was cooled to room temperature, diluted with EtOAc (50 mL), successively washed with 1 N HCl (30 mL) and brine (30 mL), dried over Na.sub.2SO.sub.4, filtered and concentrated under vacuum. The residue was purified by silica gel column chromatography to give the title compound (6.0 g, 90%). LC-MS (M+H).sup.+=327.9, 329.9, 331.9.

Step 2: 3-(3-bromo-5-(2,5-dimethyl-1H-pyrrol-1-yl)phenyl)oxetan-3-ol

[0850] ##STR00410##

[0851] To a solution of 1-(3,5-dibromophenyl)-2,5-dimethyl-1H-pyrrole (6.0 g, 18.2 mmol) in THF (20 ml), was added n-BuLi (2.5 M in hexane, 8 mL, 20.2 mmol) at ?78? C. under nitrogen. After 0.5 h, oxetan-3-one (1.9 g, 27.3 mmol) was added dropwise. The mixture was stirred at?78? C. for 1 h. Saturated NH.sub.4Cl (10 mL) was added and the mixture was warmed to room temperature then extracted with EtOAc (40 mL?2). The combined organic layer was washed with brine (50 mL?3), dried over Na.sub.2SO.sub.4, filtered and concentrated under vacuum. The residue was purified by silica gel column chromatography to give the title compound (4.0 g, 68%). LC-MS (M+H).sup.+=322.0.

Step 3: 3-(3-amino-5-bromophenyl)oxetan-3-ol

[0852] ##STR00411##

[0853] To a solution of 3-(3-bromo-5-(2,5-dimethyl-1H-pyrrol-1-yl)phenyl)oxetan-3-ol (1.0 g, 3.1 mmol) in EtOH (14 mL) and water (7 mL) was added hydroxylamine hydrochloride (6.5 g, 93 mmol) and KOH (3.4 g, 62 mmol). The mixture was heated to 10? C. for overnight then cooled to room temperature. Water (20 mL) was added and the mixture was extracted with EtOAc (40 mL?2). The combined organic layer was washed with brine (50 mL?3), dried over Na.sub.2SO.sub.4, filtered and concentrated under vacuum. The residue was purified by prep-TLC to give the title compound (700 mg, 92%). LC-MS (M+H).sup.+=244.0.

Step 4: ethyl 4-((3-bromo-5-(3-hydroxyoxetan-3-yl)phenyl)amino)butanoate

[0854] ##STR00412##

[0855] To a solution of 3-(3-amino-5-bromophenyl)oxetan-3-ol (400 mg, 1.64 mmol) in DMF (5 mL) was added K.sub.2CO.sub.3 (452 mg, 3.28 mmol) and ethyl 4-bromobutanoate (703 mg, 3.6 mmol). The mixture was stirred at 100? C. for overnight. The mixture was cooled to room temperature then water (20 mL) was added. The mixture was extracted with EtOAc (40 mL?2). The combined organic layer was washed with brine (20 mL?3), dried over Na.sub.2SO.sub.4, filter and concentrated under vacuum. The residue was purified by prep-TLC to give the title compound (120 mg, 20%). LC-MS (M+H).sup.+=358.1.

Step 5: 1-(3-bromo-5-(3-hydroxyoxetan-3-yl)phenyl)pyrrolidin-2-one

[0856] ##STR00413##

[0857] To a solution of ethyl 4-((3-bromo-5-(3-hydroxyoxetan-3-yl)phenyl)amino)butanoate (120 mg, 0.33 mmol) in 1, 4-dioxane (5 mL) was added TFA (190 mg, 1.67 mmol) and the mixture was stirred at 100? C. for overnight. The mixture was cooled to room temperature and concentrated. The crude was purified by prep-TLC to give the title compound (80 mg, 76%). LC-MS (M+H).sup.+=312.1

Step 6: 1-(3-(3-hydroxyoxetan-3-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyrrolidin-2-one

[0858] ##STR00414##

[0859] A mixture 1-(3-bromo-5-(3-hydroxyoxetan-3-yl)phenyl)pyrrolidin-2-one (80 mg, 0.25 mmol), BPD (127 mg, 0.5 mmol), Pd(dppf)Cl.sub.2 (20 mg, 0.025 mmol) and AcOK (73.5 mg, 0.75 mmol) in dioxane (10 mL) was heated to reflux under nitrogen for overnight. The mixture was cooled to room temperature, EtOAc (60 mL) was added and the organic layer was washed with brine (20 mL?2), and the combined aqueous layer was back extracted with EtOAc (30 mL). The combined organic layer was dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced to pressure. The residue was purified by prep-TLC to give the title compound (50 mg, 54%). LC-MS (M+H).sup.+=360.2.

Step 7: 1-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-(3-hydroxyoxetan-3-yl)phenyl)pyrrolidin-2-one

[0860] A mixture of 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine (50 mg, 0.14 mmol), 1-(3-(3-hydroxyoxetan-3-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyrrolidin-2-one (50 mg, 0.14 mmol), Pd(dppf)C.sub.12 (12 mg, 0.014 mmol) and K.sub.2CO.sub.3 (38 mg, 0.28 mmol) in dioxane (10 mL) and H.sub.2O (3 mL) was heated to reflux under nitrogen for overnight. The mixture was cooled to room temperature, then added EtOAc (30 mL). The mixture was washed with brine (10 mL?2), and the aqueous layer was back extracted with EtOAc (20 mL). The combined organic layer was dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure. The residue was purified by prep-HPLC to give Example A91 (13 mg, 18%). .sup.1H NMR (400 MHz, DMSO-d6) ? 8.28 (s, 1H), 8.23 (s, 1H), 8.10 (s, 1H), 7.8 (s, 1H), 7.59 (s, 1H), 6.81 (s, 2H), 6.45 (s, 1H), 4.79-4.73 (m, 4H), 4.15-4.18 (m, 1H), 3.91-3.90 (m, 2H), 2.88-2.86 (m, 2H), 2.48-2.50 (m, 2H), 2.21 (s, 3H), 2.11-1.98 (m, 8H). LC-MS (M+H).sup.+=506.2.

Example A92

3-(5-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-3-methyl-2-(7-oxa-2-azaspiro[3.5]nonan-2-yl)phenyl)tetrahydrofuran-3-ol

[0861] ##STR00415##

Step 1: 2-(2-bromo-4-chloro-6-methylphenyl)-7-oxa-2-azaspiro[3.5]nonane

[0862] ##STR00416##

[0863] The title compound (1.13 g, 63%) was prepared in a manner similar to that in Example A83 step 2 from 1-bromo-5-chloro-2-iodo-3-methylbenzene and 7-oxa-2-azaspiro[3.5]nonane. LC-MS (M+H).sup.+=330.0.

Step 2: 3-(5-chloro-3-methyl-2-(7-oxa-2-azaspiro[3.5]nonan-2-yl)phenyl)tetrahydrofuran-3-ol

[0864] ##STR00417##

[0865] The title compound (100 mg, 31%) was prepared in a manner similar to that in Example A54 step 1 from 2-(2-bromo-4-chloro-6-methylphenyl)-7-oxa-2-azaspiro[3.5]nonane and dihydrofuran-3-one. LC-MS (M+H).sup.+=338.1.

Step 3: 3-(5-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-3-methyl-2-(7-oxa-2-azaspiro[3.5]nonan-2-yl)phenyl)tetrahydrofuran-3-ol

[0866] Example A92 (32 mg, 25%) was prepared in a manner similar to that in Example A83 step 4 from 3-(5-chloro-3-methyl-2-(7-oxa-2-azaspiro[3.5]nonan-2-yl)phenyl)tetrahydrofuran-3-ol and 3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazin-2-amine. .sup.1H NMR (400 MHz, DMSO-d.sub.6) ? 8.22 (s, 1H), 8.12 (s, 1H), 7.77 (d, J=2.2 Hz, 1H), 7.59 (d, J=2.9 Hz, 2H), 6.72 (s, 2H), 6.29 (s, 1H), 4.15-4.07 (m, 1H), 4.05-3.98 (m, 1H), 4.02-3.93 (m, 1H), 3.97-3.88 (m, 1H), 3.86-3.77 (m, 3H), 3.69 (d, J=6.5 Hz, 2H), 3.59-3.52 (m, 4H), 2.90-2.83 (m, 2H), 2.56 (s, 3H), 2.43-2.31 (m, 1H), 2.21 (s, 3H), 2.19-2.10 (m, 1H), 2.10-1.94 (m, 6H), 1.85-1.78 (m, 4H). LC-MS (M+H).sup.+=576.5.

Example A93

3-(5-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2-fluoro-3-methylphenyl)tetrahydrofuran-3-ol

[0867] ##STR00418##

Step 1: 3-(5-chloro-2-fluoro-3-methylphenyl)-tetrahydrofuran-3-ol

[0868] ##STR00419##

[0869] The title compound (400 mg, 95%) was prepared in a manner similar to that in Example A54 step 1 from 1-bromo-5-chloro-2-fluoro-3-methylbenzene and dihydrofuran-3-one. LC-MS (M?OH).sup.+=213.0.

Step 2: 3-(5-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-2-fluoro-3-methylphenyl)tetrahydrofuran-3-ol

[0870] Example A93 (36 mg, 14%) was prepared in a manner similar to that in Example A83 step 4 from 3-(5-chloro-2-fluoro-3-methylphenyl)-tetrahydrofuran-3-ol and 3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazin-2-amine. .sup.1H NMR (400 MHz, DMSO-d.sub.6) ? 8.23 (s, 1H), 8.14 (s, 1H), 7.94-7.87 (m, 1H), 7.73-7.67 (m, 1H), 7.61 (s, 1H), 6.73 (s, 2H), 5.56 (s, 1H), 4.18-4.06 (m, 1H), 4.06-3.82 (m, 4H), 2.90-2.83 (m, 2H), 2.42-2.30 (m, 1H), 2.29-2.24 (m, 3H), 2.23-2.16 (m, 4H), 2.11-1.93 (m, 6H). LC-MS (M+H).sup.+=469.1.

Example A94

3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-((R)-3-methylmorpholino)phenyl)-2-methyltetrahydrofuran-3-ol

[0871] ##STR00420##

Step 1: 3-(3-bromo-5-((R)-3-methylmorpholino)phenyl)-2-methyltetrahydrofuran-3-ol

[0872] ##STR00421##

[0873] To a solution of (R)-4-(3,5-dibromophenyl)-3-methylmorpholine (570 mg, 1.7 mmol) in THF (5 mL) was added n-BuLi (2.5 M in hexane, 0.68 mL, 1.7 mmol) dropwise at ?78? C. under nitrogen, then stirred for 30 min at ?78? C. 2-methyldihydrofuran-3(2H)-one (257 mg, 2.6 mmol) was added dropwise at this temperature and stirred for another 2 h. The mixture was quenched by saturated NH.sub.4Cl (15 mL) and warmed to room temperature. The mixture was extracted with EtOAc (25 mL), successively washed with H.sub.2O (15 mL) and brine (15 mL), dried over Na.sub.2SO.sub.4, filtered and concentrated under vacuum. The residue was purified by prep-TLC with PE:EtOAc=1:3 to give the title compound (500 mg, 82%). LC-MS (M+H).sup.+=356.1, 358.1.

Step 2: 2-methyl-3-(3-((R)-3-methylmorpholino)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)tetrahydrofuran-3-ol

[0874] ##STR00422##

[0875] To a solution of 3-(3-bromo-5-((R)-3-methylmorpholino)phenyl)-2-methyltetrahydrofuran-3-ol (500 mg, 1.4 mmol) in dioxane (10 mL) was added BPD (715 mg, 2.8 mmol), KOAc (275 mg, 2.8 mmol) and Pd(dppf)Cl.sub.2.Math.CH.sub.2Cl.sub.2 (115 mg, 0.1 mmol), then the mixture stirred for overnight at 100? C. under nitrogen. The mixture was cooled to room temperature, diluted with EtOAc (30 mL), washed with H.sub.2O (15 mL), brine (15 mL), dried over Na.sub.2SO.sub.4, filtered and concentrated under vacuum. The residue was purified by prep-TLC with EtOAc to give the title compound (550 mg, 97%). LC-MS (M+H).sup.+=404.4.

Step 3: 3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-((R)-3-methylmorpholino)phenyl)-2-methyltetrahydrofuran-3-ol

[0876] To a solution of 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine (480 mg, 1.4 mmol) in dioxane (10 mL) and water (1 mL) were added 2-methyl-3-(3-((R)-3-methylmorpholino)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)tetrahydrofuran-3-ol (550 mg, 1.4 mmol), K.sub.2CO.sub.3 (565 mg, 4.1 mmol) and Pd(dppf)Cl.sub.2.Math.CH.sub.2Cl.sub.2 (112 mg, 0.14 mmol), then the mixture stirred for 5 h at 100? C. under nitrogen. The mixture was cooled to room temperature and diluted with EtOAc (40 mL). The organic layer was washed with H.sub.2O (20 mL), brine (20 mL), dried over Na.sub.2SO.sub.4, filtered and concentrated under vacuum. The residue was purified by prep-TLC with MeOH:DCM=1:7, then by prep-HPLC to give Example A94 (66 mg, 9%). .sup.1H NMR (400 MHz, DMSO-d.sub.6) ? 8.25 (s, 1H), 8.13 (s, 1H), 7.57 (s, 1H), 7.41-7.36 (m, 1H), 7.19 (s, 1H), 7.04-6.98 (m, 1H), 6.69 (s, 2H), 5.10 (s, 1H), 4.14-4.04 (m, 1H), 4.04-3.96 (m, 1H), 3.95-3.85 (m, 3H), 3.84-3.78 (m, 1H), 3.77-3.68 (m, 2H), 3.62-3.53 (m, 1H), 3.23-3.17 (m, 1H), 3.09-3.00 (m, 1H), 2.90-2.82 (m, 2H), 2.21 (s, 3H), 2.16-1.94 (m, 7H), 0.98 (d, J=6.5 Hz, 3H), 0.94 (d, J=6.1 Hz, 3H). LC-MS (M+H).sup.+=550.3.

Example A95A/A95B

(2R,3S)-3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-((R)-3-methylmorpholino)phenyl)-2-methyltetrahydrofuran-3-ol & (2S,3R)-3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-((R)-3-methylmorpholino)phenyl)-2-methyltetrahydrofuran-3-ol

[0877] ##STR00423##

[0878] Examples A95A/A95B were prepared by chiral-HPLC separation of 3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-((R)-3-methylmorpholino)phenyl)-2-methyltetrahydrofuran-3-ol (66 mg). Analytical chiral-HPLC condition: CHIRALPAK IA3, 4.6?50 mm, 3 ?m; (hexane, contains 0.5% 2 M NH.sub.3 in MeOH):EtOH=7:3; 1 mL/min: 25? C.

[0879] Example A95A: (23 mg, 35%) .sup.1H NMR (400 MHz, DMSO-d.sub.6) ? 8.25 (s, 1H), 8.13 (s, 1H), 7.57 (s, 1H), 7.41-7.36 (m, 1H), 7.19 (s, 1H), 7.04-6.98 (m, 1H), 6.69 (s, 2H), 5.10 (s, 1H), 4.14-4.04 (m, 1H), 4.04-3.96 (m, 1H), 3.95-3.85 (m, 3H), 3.84-3.78 (m, 1H), 3.77-3.68 (m, 2H), 3.62-3.53 (m, 1H), 3.23-3.17 (m, 1H), 3.09-3.00 (m, 1H), 2.90-2.82 (m, 2H), 2.23 (s, 3H), 2.16-1.94 (m, 7H), 0.98 (d, J=6.5 Hz, 3H), 0.94 (d, J=6.1 Hz, 3H). LC-MS (M+H).sup.+=550.3. Chiral HPLC: tR=2.19 min.

[0880] Example A95B: (23 mg, 35%).sup.1H NMR (400 MHz, DMSO-d.sub.6) ? 8.25 (s, 1H), 8.12 (s, 1H), 7.57 (s, 1H), 7.41-7.36 (m, 1H), 7.19 (s, 1H), 7.04-6.98 (m, 1H), 6.69 (s, 2H), 5.10 (s, 1H), 4.14-4.04 (m, 1H), 4.04-3.96 (m, 1H), 3.95-3.85 (m, 3H), 3.84-3.78 (m, 1H), 3.77-3.68 (m, 2H), 3.62-3.53 (m, 1H), 3.25-3.17 (m, 1H), 3.09-3.00 (m, 1H), 2.93-2.82 (m, 2H), 2.22 (s, 3H), 2.16-1.94 (m, 7H), 0.98 (d, J=6.5 Hz, 3H), 0.94 (d, J=6.1 Hz, 3H). LC-MS (M+H).sup.+=550.3. Chiral HPLC: tR=2.99 min.

Example A96

3-(5-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-3-methyl-2-morpholinophenyl)tetrahydrofuran-3-ol

[0881] ##STR00424##

Step 1: 4-(2-bromo-4-chloro-6-methylphenyl)morpholine

[0882] ##STR00425##

[0883] A mixture of 1-bromo-5-chloro-2-iodo-3-methylbenzene (3.0 mg, 8.3 mmol), Pd.sub.2(dba).sub.3 (241 mg, 0.25 mmol), XantPhos (304 mg, 0.50 mmol), t-BuONa (927 mg, 9.2 mmol) and morpholine (764 mg, 8.3 mmol) in toluene (30 mL) was stirred for 16 h at 110? C. under nitrogen. The mixture was filtered, and the filter cake was washed with DCM (15 mL?3). The filtrate was concentrated under reduced pressure. The residue was purified by reverse phase flash chromatography to give the title compound (820 mg, 31%). LC-MS (M+H).sup.+=291.9.

Step 2: 4-(4-chloro-2-(2,5-dihydrofuran-3-yl)-6-methylphenyl)morpholine

[0884] ##STR00426##

[0885] The title compound (473 mg, 47%) was prepared in a manner similar to that in Example A75 step 1 from 4-(2-bromo-4-chloro-6-methylphenyl)morpholine and 2-(2,5-dihydrofuran-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane. LC-MS (M+H).sup.+=280.1.

Step 3: 3-(5-chloro-3-methyl-2-morpholinophenyl)tetrahydrofuran-3-ol

[0886] ##STR00427##

[0887] At 0? C., to a solution of tris(2,2,6,6-tetramethyl-3,5-heptanedionato)manganese(III) (108 mg, 0.17 mmol) and 4-(4-chloro-2-(2,5-dihydrofuran-3-yl)-6-methylphenyl)morpholine (500 mg, 1.70 mmol) in DCM (5 mL) was added i-PrOH (3.5 mL), phenylsilane (387 mg, 3.40 mmol). The mixture was stirred for 3 h at 0? C. under oxygen. The mixture was concentrated under vacuum. The residue was purified by reverse phase chromatography to give the title compound (170 mg, 34%). LC-MS (M+H).sup.+=298.2.

Step 4: 3-(5-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-3-methyl-2-morpholinophenyl)tetrahydrofuran-3-ol

[0888] Example A96 (90 mg, 35%) was prepared in a manner similar to that in Example A83 step 4 from 3-(5-chloro-3-methyl-2-morpholinophenyl)tetrahydrofuran-3-ol and 3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazin-2-amine. .sup.1H NMR (400 MHz, DMSO-d.sub.6) ? 8.23 (s, 1H), 8.11 (s, 1H), 7.76 (s, 1H), 7.61-7.55 (m, 2H), 6.72 (s, 2H), 5.95 (s, 1H), 4.36-4.29 (m, 1H), 4.17-4.07 (m, 1H), 3.99-3.89 (m, 2H), 3.87-3.81 (m, 1H), 3.81-3.74 (m, 2H), 3.70-3.59 (m, 2H), 3.56-3.46 (m, 1H), 3.39-3.34 (m, 1H), 2.91-2.82 (m, 3H), 2.74-2.67 (m, 1H), 2.43 (s, 3H), 2.42-2.31 (m, 1H), 2.30-2.23 (m, 1H), 2.21 (s, 3H), 2.07-1.96 (m, 6H). LC-MS (M+H).sup.+=536.4.

Example A97A/A97B

(S)-3-(5-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-3-methyl-2-morpholinophenyl)tetrahydrofuran-3-ol & (R)-3-(5-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-3-methyl-2-morpholinophenyl)tetrahydrofuran-3-ol

[0889] ##STR00428##

[0890] Examples A97A/A97B were prepared by chiral-HPLC separation of 3-(5-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-3-methyl-2-morpholinophenyl)tetrahydrofuran-3-ol (58 mg). Analytical chiral-HPLC condition: CHIRALPAK IA3, 4.6?50 mm, 3 ?m; (hexane:DCM=3:1, contains 0.1% Et.sub.2NH):EtOH=7:3; 1 mL/min: 25? C.

[0891] Example A97A: (26 mg, 45%).sup.1H NMR (400 MHz, DMSO-d.sub.6) ? 8.23 (s, 1H), 8.10 (s, 1H), 7.76 (s, 1H), 7.61-7.55 (m, 2H), 6.72 (s, 2H), 5.95 (s, 1H), 4.35-4.29 (m, 1H), 4.15-4.07 (m, 1H), 3.99-3.87 (m, 2H), 3.87-3.81 (m, 1H), 3.81-3.73 (m, 2H), 3.70-3.59 (m, 2H), 3.56-3.45 (m, 1H), 3.42-3.30 (m, 1H), 2.91-2.82 (m, 3H), 2.74-2.66 (m, 1H), 2.43 (s, 3H), 2.42-2.31 (m, 1H), 2.31-2.22 (m, 1H), 2.20 (s, 3H), 2.09-1.93 (m, 6H). LC-MS (M+H).sup.+=536.4. Chiral HPLC: tR=1.54 min.

[0892] Example A97B: (26 mg, 45%) .sup.1H NMR (400 MHz, DMSO-d.sub.6) ? 8.23 (s, 1H), 8.10 (s, 1H), 7.76 (s, 1H), 7.61-7.55 (m, 2H), 6.72 (s, 2H), 5.95 (s, 1H), 4.36-4.29 (m, 1H), 4.17-4.07 (m, 1H), 3.99-3.87 (m, 2H), 3.87-3.81 (m, 1H), 3.81-3.73 (m, 2H), 3.70-3.59 (m, 2H), 3.56-3.45 (m, 1H), 3.42-3.32 (M, 1H), 2.91-2.83 (m, 3H), 2.74-2.67 (m, 1H), 2.43 (s, 3H), 2.39-2.31 (M, 1H), 2.31-2.23 (m, 1H), 2.21 (s, 3H), 2.09-1.94 (m, 6H). LC-MS (M+H).sup.+=536.4. Chiral HPLC: tR=2.14 min.

Example A98

3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-(1,4-oxazepan-4-yl)phenyl)tetrahydrofuran-3-ol

[0893] ##STR00429##

Step 1: 4-(3,5-dibromophenyl)-1,4-oxazepane

[0894] ##STR00430##

[0895] The title compound (365 mg, 42%) was prepared in a manner similar to that in Example A59 step 1 from 1,3-dibromo-5-iodobenzene and 1,4-oxazepane. LC-MS (M+H).sup.+=335.9.

Step 2: 3-(3-bromo-5-(1,4-oxazepan-4-yl)phenyl)tetrahydrofuran-3-ol

[0896] ##STR00431##

[0897] The title compound (83 mg, 50%) was prepared in a manner similar to that Example A54 step 1 from 4-(3,5-dibromophenyl)-1,4-oxazepane and dihydrofuran-3-one. LC-MS (M+H).sup.+=342.0.

Step 3: 3-(3-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-5-(1,4-oxazepan-4-yl)phenyl)tetrahydrofuran-3-ol

[0898] Example A98 (27 mg, 22%) was prepared in a manner similar to that in Example A83 step 4 from 3-(3-bromo-5-(1,4-oxazepan-4-yl)phenyl)tetrahydrofuran-3-ol and 3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazin-2-amine. .sup.1H NMR (400 MHz, DMSO-d.sub.6) ? 8.22 (s, 1H), 8.07 (s, 1H), 7.59 (s, 1H), 7.19 (s, 1H), 7.05 (s, 1H), 6.81 (s, 1H), 6.65 (s, 2H), 5.29 (s, 1H), 4.14-3.95 (m, 3H), 3.82-3.73 (m, 2H), 3.76-3.69 (m, 2H), 3.65-3.53 (m, 6H), 2.89-2.82 (m, 2H), 2.35-2.23 (m, 1H), 2.20 (s, 3H), 2.14-1.86 (m, 10H). LC-MS (M+H).sup.+=536.4.

Example B1

5-(2-(diethylamino)-6-((methylamino)methyl)pyridin-4-yl)-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine

[0899] ##STR00432##

Step 1: methyl 4-chloro-6-(diethylamino)picolinate

[0900] ##STR00433##

[0901] To a solution of methyl 4,6-dichloropyridine-2-carboxylate (4.0 g, 18.4 mmol) in toluene (25 mL) was added diethylamine (11.4 g, 148 mmol), Pd(OAc).sub.2 (218 mg, 0.922 mmol), XPhos (1481 mg, 2.95 mmol) and K.sub.2CO.sub.3 (4025 mg, 27.7 mmol) at room temperature. The mixture was stirred for overnight at 100? C. under nitrogen. The mixture was cooled to room temperature and concentrated under reduced pressure. The residue was purified by silica gel chromatography (EtOAc:hexanes=1:4) to give the title compound (2.1 g, 47%). LC-MS (M+H).sup.+=243.2.

Step 2: (4-chloro-6-(diethylamino)pyridin-2-yl)methanol

[0902] ##STR00434##

[0903] To a solution of methyl 4-chloro-6-(diethylamino)picolinate (2.20 g, 8.36 mmol) in THF (20 mL) was added BH.sub.3 in THF (1 M, 28.7 mL, 28.7 mmol) dropwise over 5 min at 0? C. The mixture was heated to 70? C. under nitrogen. After 2 h, the mixture was cooled 0? C., was then MeOH (5 mL) was carefully added. The mixture was concentrated under reduced pressure and the residue was purified by silica gel chromatography (EtOAc:hexanes=1:4) to give the title compound (1.47 g, 82%). LC-MS (M+H).sup.+=215.2.

Step 3: 4-chloro-6-(diethylamino)picolinaldehyde

[0904] ##STR00435##

[0905] To a solution of (4-chloro-6-(diethylamino)pyridin-2-yl)methanol (1.50 g, 6.24 mmol) in DCM (20 mL) was added Dess-Martin periodinane (7.96 g, 17.8 mmol) at room temperature. After 2 h, saturated NaHCO.sub.3 (10 mL) and saturated Na.sub.2S.sub.2O.sub.3 (10 mL) was added at 0? C. The mixture was extracted with EtOAc (30 mL?3). The combined organic layer was washed with brine (30 mL), dried over Na.sub.2SO.sub.4 and filtered. The filtrate was concentrated under reduced pressure to give the title compound (1.24 g, 93%). LC-MS (M+H).sup.+=213.2.

Step 4: 4-chloro-N,N-diethyl-6-((methylamino)methyl)pyridin-2-amine

[0906] ##STR00436##

[0907] To a stirred solution of 4-chloro-6-(diethylamino)picolinaldehyde (1.16 g, 5.437 mmol) and methylamine in THF (2 M, 3.9 mL, 7.8 mmol) in MeOH (15 mL) was added HOAc (1 mL) at room temperature. After 15 min, the solution was cooled to 0? C., and NaBH.sub.3CN (0.58 g, 8.8 mmol) was added in portions. The mixture was warmed to room temperature and stirred for 1 h, then cooled back to 0? C. Water (50 mL) was added and the mixture was extracted with EtOAc (30 mL?3). The combined organic layers were washed with brine (10 mL?3), dried over anhydrous Na.sub.2SO.sub.4 and filtered. The filtrate was concentrated under reduced pressure to give the title compound (1.1 g, 88%). LC-MS (M+H).sup.+=228.3.

Step 5: tert-butyl ((4-chloro-6-(diethylamino)pyridin-2-yl)methyl)(methyl)carbamate

[0908] ##STR00437##

[0909] The title compound (400 mg, 88%) was prepared in a manner similar to that in Example A20 step 1 from 4-chloro-N,N-diethyl-6-((methylamino)methyl)pyridin-2-amine. LC-MS (M+H).sup.+=328.3.

Step 6: tert-butyl ((6-(diethylamino)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)methyl)(methyl)carbamate

[0910] ##STR00438##

[0911] The title compound (249 mg, 52%) was prepared in a manner similar to that in Example A1 step 6 from tert-butyl ((4-chloro-6-(diethylamino)pyridin-2-yl)methyl)(methyl)carbamate and BPD. LC-MS (M+H).sup.+=420.4.

Step 7: tert-butyl ((4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-6-(diethylamino)pyridin-2-yl)methyl)(methyl)carbamate

[0912] ##STR00439##

[0913] The title compound (35 mg, 34%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and tert-butyl ((6-(diethylamino)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)methyl)(methyl)carbamate. LC-MS (M+H).sup.+=566.5.

Step 2: 5-(2-(diethylamino)-6-((methylamino)methyl)pyridin-4-yl)-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine

[0914] Example B1 (3 mg, 11%) was prepared in a manner similar to that in Example A20 step 4 from tert-butyl ((4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-6-(diethylamino)pyridin-2-yl)methyl)(methyl)carbamate. .sup.1H NMR (400 MHz, DMSO-d6) ? 8.30 (s, 1H), 8.06 (s, 1H), 7.61 (s, 1H), 6.98 (s, 1H), 6.90 (s, 2H), 6.80 (s, 1H), 4.14-4.03 (m, 1H), 3.57 (s, 2H), 3.55-3.45 (m, 4H), 2.90-2.82 (m, 2H), 2.33 (s, 3H), 2.20 (s, 3H), 2.09-1.90 (m, 6H), 1.10 (t, J=6.9 Hz, 6H). LC-MS (M+H).sup.+=466.3.

Example B2

(R)-5-(2-((methylamino)methyl)-6-(2-methylpyrrolidin-1-yl)pyridin-4-yl)-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine

[0915] ##STR00440##

Step 1: methyl (R)-4-chloro-6-(2-methylpyrrolidin-1-yl)picolinate

[0916] ##STR00441##

[0917] The title compound (1.8 g, 31%) was prepared in a manner similar to that in Example B1 step 1 from methyl 4,6-dichloropyridine-2-carboxylate and (2R)-2-methylpyrrolidine. LC-MS (M+H).sup.+=255.2.

Step 2: (R)-(4-chloro-6-(2-methylpyrrolidin-1-yl)pyridin-2-yl)methanol

[0918] ##STR00442##

[0919] The title compound (1.1 g, 68%) was prepared in a manner similar to that in Example B1 step 2 from methyl (R)-4-chloro-6-(2-methylpyrrolidin-1-yl)picolinate. LC-MS (M+H).sup.+=227.2.

Step 3: (R)-4-chloro-6-(2-methylpyrrolidin-1-yl)picolinaldehyde

[0920] ##STR00443##

[0921] The title compound (864 mg, 85%) was prepared in a manner similar to that in Example B1 step 3 from (R)-(4-chloro-6-(2-methylpyrrolidin-1-yl)pyridin-2-yl)methanol. LC-MS (M+H).sup.+=225.2.

Step 4: (R)-1-(4-chloro-6-(2-methylpyrrolidin-1-yl)pyridin-2-yl)-N-methylmethanamine

[0922] ##STR00444##

[0923] The title compound (864 mg, 85%) was prepared in a manner similar to that in Example B1 step 4 from (R)-4-chloro-6-(2-methylpyrrolidin-1-yl)picolinaldehyde. LC-MS (M+H).sup.+=240.2.

Step 5: tert-butyl (R)-((4-chloro-6-(2-methylpyrrolidin-1-yl)pyridin-2-yl)methyl)(methyl)carbamate

[0924] ##STR00445##

[0925] The title compound (1.05 g, 86%) was prepared in a manner similar to that in Example A20 step 1 from (R)-1-(4-chloro-6-(2-methylpyrrolidin-1-yl)pyridin-2-yl)-N-methylmethanamine. LC-MS (M+H).sup.+=340.2.

Step 6: tert-butyl (R)-methyl((6-(2-methylpyrrolidin-1-yl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)methyl)carbamate

[0926] ##STR00446##

[0927] The title compound (473 mg, 87%) was prepared in a manner similar to that in Example A1 step 6 from tert-butyl (R)-((4-chloro-6-(2-methylpyrrolidin-1-yl)pyridin-2-yl)methyl)(methyl)carbamate and BPD. LC-MS (M?pin).sup.+=350.3.

Step 7: tert-butyl (R)-((4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-6-(2-methylpyrrolidin-1-yl)pyridin-2-yl)methyl)(methyl)carbamate

[0928] ##STR00447##

[0929] The title compound (94 mg, 46%) was prepared in a manner similar to that in Example A1 step 7 from tert-butyl (R)-methyl((6-(2-methylpyrrolidin-1-yl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)methyl)carbamate and 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine. LC-MS (M+H).sup.+=578.4.

Step 8: (R)-5-(2-((methylamino)methyl)-6-(2-methylpyrrolidin-1-yl)pyridin-4-yl)-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine

[0930] Example B2 (6 mg, 7%) was prepared in a manner similar to that in Example A20 step 4 from tert-butyl (R)-((4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-6-(2-methylpyrrolidin-1-yl)pyridin-2-yl)methyl)(methyl)carbamate. .sup.1H NMR (400 MHz, DMSO-d.sub.6) ? 8.31 (s, 1H), 8.11 (s, 1H), 7.73 (s, 1H), 6.99 (s, 1H), 6.94 (s, 2H), 6.84 (s, 1H), 4.45-4.37 (m, 2H), 3.58 (s, 3H), 3.55-3.47 (m, 4H), 3.10 (t, J=6.4 Hz, 2H), 2.34 (s, 3H), 1.12 (t, J=7.0 Hz, 6H). LC-MS (M+H).sup.+=478.4.

Example B3

(R)-2-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-6-(3-methylmorpholino)pyridin-2-yl)propan-2-ol

[0931] ##STR00448##

Step 1: methyl 4-chloro-6-fluoropicolinate

[0932] ##STR00449##

[0933] To a solution of methyl 4-chloropyridine-2-carboxylate (5.0 g, 27.7 mmol) in acetonitrile (120 mL) was added AgF (5.55 g, 41.5 mmol) at room temperature under nitrogen. After 24 h, mixture was concentrated under vacuum. The residue was purified by silica gel chromatography, eluting with EtOAc in PE (0% to 50% gradient) to give the title compound (4.17 g, 80%). LC-MS (M+H).sup.+=189.9.

Step 2: (R)-methyl 4-chloro-6-(3-methylmorpholino)picolinate

[0934] ##STR00450##

[0935] A mixture of methyl 4-chloro-6-fluoropyridine-2-carboxylate (1.36 g, 7.2 mmol), DIPEA (2.63 mL, 14.3 mmol) and (3R)-3-methylmorpholine (840 mg, 7.9 mmol) in DMSO (20 mL) was stirred at 50? C. under nitrogen. The mixture was cooled to room temperature, diluted with brine (30 mL), and successively extracted with EtOAc (30 mL?2). The combined organic layer was dried over Na.sub.2SO.sub.4, filtered and the filtrate was concentrated under reduced pressure. The residue was purified by reverse flash chromatography to give the title compound (864 mg, 44%). LC-MS (M+H).sup.+=270.9.

Step 3: (R)-2-(4-chloro-6-(3-methylmorpholino)pyridin-2-yl)propan-2-ol

[0936] ##STR00451##

[0937] At 0? C., to a solution of (R)-methyl 4-chloro-6-(3-methylmorpholino)picolinate (700 mg, 2.48 mmol) in ethyl ether (10 mL) was added MeMgBr in ethyl ether (3.0 M, 2.2 mL, 6.6 mmol) dropwise under nitrogen. The mixture was stirred for 2 h at 0? C. The mixture was quenched with sat. NH.sub.4C.sub.1 (10 mL). The aqueous layer was extracted with EtOAc (20 mL?3). The combined organic layer was concentrated under reduced pressure. The residue was purified by silica gel chromatography, eluting with EtOAc in PE (0% to 50% gradient) to give the title compound (500 mg, 74%). LC-MS (M+H).sup.+=271.0.

Step 4: (R)-2-(6-(3-methylmorpholino)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)propan-2-ol

[0938] ##STR00452##

[0939] The title compound (276 mg, 69%) was prepared in a manner similar to that in Example A1 step 6 from (R)-2-(4-chloro-6-(3-methylmorpholino)pyridin-2-yl)propan-2-ol and BPD. LC-MS (M+H).sup.+=362.2.

Step 5: (R)-2-(4-(5-amino-6-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-yl)-6-(3-methylmorpholino)pyridin-2-yl)propan-2-ol

[0940] Example B3 (32 mg, 22%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and (R)-2-(6-(3-methylmorpholino)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)propan-2-ol. .sup.1H NMR (400 MHz, DMSO-d.sub.6) ? 8.35 (s, 1H), 8.15 (s, 1H), 7.59 (s, 1H), 7.38 (s, 1H), 7.00-6.88 (m, 3H), 5.07 (s, 1H), 4.42-4.34 (m, 1H), 4.16-4.06 (m, 1H), 3.99-3.82 (m, 2H), 3.78-3.60 (m, 2H), 3.58-3.46 (m, 1H), 3.14-3.01 (m, 1H), 2.92-2.82 (m, 2H), 2.22 (s, 3H), 2.12-1.90 (m, 6H), 1.42 (s, 6H), 1.11 (d, J=6.5 Hz, 3H). LC-MS (M+H).sup.+=509.4.

Example B4

(R)-3-(4-(5-amino-6-(1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yloxy)pyrazin-2-yl)-6-(3-methylmorpholino)pyridin-2-yl)oxetan-3-ol

[0941] ##STR00453##

Step 1: (R)-4-(6-bromo-4-chloropyridin-2-yl)-3-methylmorpholine

[0942] ##STR00454##

[0943] The title compound (2.4 g, 59%) was prepared in a manner similar to that in B1 step 1 from 2,6-dibromo-4-chloropyridine and (3R)-3-methylmorpholine. LC-MS (M+H).sup.+=291.0.

Step 2: (R)-3-(4-chloro-6-(3-methylmorpholino)pyridin-2-yl)oxetan-3-ol

[0944] ##STR00455##

[0945] The title compound (280 mg, 48%) was prepared in a manner similar to that in Example A54 step 1 from (R)-4-(6-bromo-4-chloropyridin-2-yl)-3-methylmorpholine and 3-oxetanone. LC-MS (M+H).sup.+=285.1.

Step 3: (R)-3-(6-(3-methylmorpholino)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)oxetan-3-ol

[0946] ##STR00456##

[0947] The title compound (90 mg, 69%) was prepared in a manner similar to that in Example A1 step 6 from (R)-3-(4-chloro-6-(3-methylmorpholino)pyridin-2-yl)oxetan-3-ol and BPD. LC-MS (M+H).sup.+=295.2.

Step 4: (R)-3-(4-(5-amino-6-(1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yloxy)pyrazin-2-yl)-6-(3-methylmorpholino)pyridin-2-yl)oxetan-3-ol (Compound 4, 005-2468-0)

[0948] ##STR00457##

[0949] Example B4 (26 mg, 22%) was prepared in a manner similar to that in Example A1 step 7 from 5-bromo-3-((1-(1-methylpiperidin-4-yl)-1H-pyrazol-4-yl)oxy)pyrazin-2-amine and (R)-3-(6-(3-methylmorpholino)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)oxetan-3-ol. .sup.1H NMR (300 MHz, DMSO-d.sub.6) ? 8.36 (s, 1H), 8.10 (s, 1H), 7.56 (s, 1H), 7.33 (s, 1H), 7.05 (s, 1H), 6.96 (s, 2H), 6.30 (s, 1H), 4.94-4.86 (m, 2H), 4.62-4.54 (m, 2H), 4.49-4.41 (m, 1H), 4.16-400 (m, 1H), 4.00-3.89 (m, 2H), 3.79-3.70 (m, 1H), 3.70-3.60 (m, 1H), 3.58-3.44 (m, 1H), 3.17-3.03 (m, 1H), 2.91-2.81 (m, 2H), 2.20 (s, 3H), 2.11-1.84 (m, 6H), 1.13 (d, J=6.6 Hz 3H). LC-MS (M+H).sup.+=523.4.

Biological Activity

HPK Kinase Activity Assay at 1 mM ATP

HPK Kinase Activity Assay at 1 mM ATP

[0950] Compounds disclosed herein were tested for inhibition of HPK1 kinase (aal-346. Life Technologies) activity in assays based on the time-resolved fluorescence-resonance energy transfer (TR-FRET) methodology. The assays were carried out in 384-well low volume black plates in a reaction mixture containing HPK1 kinase (40 nM), 1 mM ATP, 0.5 ?M STK1 substrate and 0-10 ?M compound in buffer containing 50 mM HEPES, 0.01% BSA, 0.1 mM Orthovanadate, 10 mM MgCl.sub.2, 1 mM DTT, pH=7.0, 0.005% Tween-20. The kinase was incubated with the compounds disclosed herein or DMSO for 60 minutes at room temperature and the reaction was initiated by the addition of ATP and STK1 substrate. After reaction at room temperature for 120 minutes an equal volume of stop/detection solution was added according to the manufacture's instruction (CisBio). The stop/detection solution contained STY Antibody-Cryptate and XL665-conjugated streptavidin in Detection Buffer. The TR-FRET signals (ratio of fluorescence emission at 665 nm over emission at 620 nm with excitation at 337 nm wavelength) were recorded on a PHERAstar FS plate reader (BMG Labtech). Phosphorylation of STK1 substrate led to the binding of STK Antibody-Cryptate to the biotinylated STK1 substrate, which places fluorescent donor (Eu.sup.3+ crypate) in close proximity to the accepter (Streptavidin-XL665), thus resulting in a high degree of fluorescence resonance energy transfer. The inhibition of HPK1 in presence of increasing concentrations of compounds was calculated based on the ratio jo of fluorescence at 665 nm to that at 620 nm. IC.sub.50 determination was performed by fitting the curve of percent inhibition versus the log of the inhibitor concentration using Dotmatics. The compounds disclosed herein showed the enzymatic activity values as in Table 1.

TABLE-US-00001 TABLE 1 Enzymatic activity IC.sub.50 (nM) for the compounds disclosed herein Enzymatic activity Enzymatic activity Example IC.sub.50 (nM) Example IC.sub.50 (nM) A1 47 A2 14 A3 110 A4 25 A5 35 A6 44 A7 20 A8 8 A9 46 A10 44 A11 9 A12 127 A13 139 A14 45 A15 83 A16 18 A17 59 A18 100 A19 44 A20 70 A21 104 A22 14 A23 6 A24 104 A25 14 A26 30 A27 57 A28 50 A29 21 A30 111 A31 34 A32 30 A33 67 A34 65 A35 47 A36 22 A37 17 A38 37 A39 35 A40 33 A41 11 A42 19 A43 6 A44 9 A45 51 A46 51 A47 68 A48 50 A49 11 A50 18 A51 46 A52 70 A53 16 A54 10 A55 34 A56 53 A57 24 A58 29 A59 8.2 A60 40 A61A 253 A61B 10 A62 48 A63 39 A64 16 A65 18 A66 36 A67 17 A68 51 A69 57 A70 6.7 A71 26 A72 5.6 A73 11 A74A 46 A74B 10 A75 29 A76 5.8 A77 38 A78 5.5 A79 12 A80A 29 A80B 5.4 A81 37 A82 37 A83 17 A84 58 A85 3.7 A86 40 A87 56 A88 34 A89 11 A90A 82 A90B 7.1 A91 11 A92 7.0 A93 37 A94 15 A95A 44 A95B 4.5 A96 36 A97A 18 A97B 30 A98 9.2 B1 26 B2 12 B3 11 B4 31
Cellular pSLP76(S376) HTRF Assay

[0951] Jurkat cell line was used in this study. Cells were maintained in RPMI 1640 supplemented with heat-inactivated 10% fetal bovine serum (Thermo Fisher), 50 units/mL penicillin and streptomycin (Thermo Fisher) and kept at 37? C. in a humidified atmosphere of 5% CO.sub.2 in air. Cells were reinstated from frozen stocks that were laid down within 30 passages from the original cells purchased. After cell starvation in the assay buffer (RPMI 1640 supplemented with heat-inactivated 0.1% fetal bovine serum) for 18 hours, cells were seeded into a round bottom 96-well plate at 150,000 cells per well density. Cells were treated with a 9-point dilution series of test compounds. The final compound concentration is from 0 to 2 ?M. After 2 h compound treatment, cells were stimulated with 0.05 ?g/mL anti-human CD.sub.3 (OKT3, Bioxcell) for 30 min at 37? C. Then the cells were lysed, and the pSLP76(S376) level in the cell lysates was detected by HTRF kit (Cisbio). A total of 16 ?L of cell lysate from each well of a 96-well plate was transferred to a 384-well small volume white assay plate. Lysate from each well was incubated with 2 ?L of Eu.sup.3+-cryptate (donor) labeled anti-phospho-SLP376 and 2 ?L of D2 (acceptor) labeled anti-phospho-SLP376 antibodies (Cisbio) overnight in dark at room temperature. FRET signals (655 nm) were measured using a PHERAstar FSX reader (BMG Labtech). IC.sub.50 determination was performed by fitting the curve of percent inhibition versus the log of the inhibitor concentration using Dotmatics. The compounds disclosed herein showed the cellular activity values as in Table 2.

TABLE-US-00002 TABLE 2 Cellular activity IC.sub.50 (nM) for the compounds disclosed herein Cellular activity Cellular activity Example IC.sub.50 (nM) Example IC.sub.50 (nM) A1 93 A2 34 A3 150 A4 91 A5 70 A6 35 A7 62 A8 30 A9 99 A10 117 A11 54 A12 119 A13 120 A14 59 A15 157 A16 80 A17 194 A18 47 A19 46 A20 97 A21 188 A22 38 A23 35 A24 175 A25 62 A26 82 A27 81 A28 97 A29 97 A30 330 A31 77 A32 81 A33 102 A34 155 A35 123 A36 54 A37 98 A38 125 A39 176 A40 125 A41 101 A42 82 A43 26 A44 61 A45 119 A46 98 A47 183 A48 183 A49 82 A50 95 A51 101 A52 118 A53 63 A54 33 A55 111 A56 85 A57 76 A58 69 A59 51 A60 91 A61B 44 A62 79 A63 102 A64 45 A65 84 A66 132 A67 76 A68 157 A69 84 A70 76 A71 39 A72 59 A73 59 A74A 85 A74B 41 A75 129 A76 62 A77 91 A78 51 A79 71 A80A 194 A80B 48 A81 72 A82 125 A83 105 A84 83 A85 28 A86 130 A87 89 A88 85 A89 64 A90B 100 A91 199 A92 156 A93 164 A94 119 A95A 124 A95B 68 A96 117 A97A 78 A97B 154 A98 73 B1 181 B2 121 B3 229 B4 102

[0952] It is to be understood that, it any prior art publication is referred to herein: such reference does not constitute an admission that the publication forms a part of the common general knowledge in the art in any country.

[0953] The disclosures of all publications, patents, patent applications and published patent applications referred to herein by an identifying citation are hereby incorporated herein by reference in their entirety.

[0954] Although the foregoing invention has been described in some detail by way of illustration and example for purposes of clarity of understanding, it is apparent to those skilled in the art that certain minor changes and modifications will be practiced. Therefore, the description and Examples should not be construed as limiting the scope of the invention.