WO2013102431A1 - Therapeutically active compounds and their methods of use - Google Patents

Therapeutically active compounds and their methods of use Download PDF

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Publication number
WO2013102431A1
WO2013102431A1 PCT/CN2013/000009 CN2013000009W WO2013102431A1 WO 2013102431 A1 WO2013102431 A1 WO 2013102431A1 CN 2013000009 W CN2013000009 W CN 2013000009W WO 2013102431 A1 WO2013102431 A1 WO 2013102431A1
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WO
WIPO (PCT)
Prior art keywords
alkyl
phenyl
alkylene
compound
pyridin
Prior art date
Application number
PCT/CN2013/000009
Other languages
French (fr)
Inventor
Giovanni Cianchetta
Byron Delabarre
Janeta Popovici-Muller
Francesco G. Salituro
Jeffrey O. Saunders
Jeremy Travins
Shunqi Yan
Tao Guo
Li Zhang
Original Assignee
Agios Pharmaceuticals, Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=48744984&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=WO2013102431(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority to CN202210633951.7A priority Critical patent/CN115521264A/en
Priority to CN201380009314.1A priority patent/CN104114543B/en
Priority to MYPI2014002013A priority patent/MY185206A/en
Application filed by Agios Pharmaceuticals, Inc. filed Critical Agios Pharmaceuticals, Inc.
Priority to AU2013207289A priority patent/AU2013207289B2/en
Priority to RS20180756A priority patent/RS57401B1/en
Priority to JP2014550627A priority patent/JP6411895B2/en
Priority to SI201331050T priority patent/SI2800743T1/en
Priority to EP18164959.1A priority patent/EP3406608B8/en
Priority to DK13733752.3T priority patent/DK2800743T3/en
Priority to CA2860623A priority patent/CA2860623A1/en
Priority to LTEP13733752.3T priority patent/LT2800743T/en
Priority to SG11201403878QA priority patent/SG11201403878QA/en
Priority to BR112014016805-9A priority patent/BR112014016805B1/en
Priority to CN201810599955.1A priority patent/CN108912066B/en
Priority to ES13733752.3T priority patent/ES2675760T3/en
Priority to EA201491330A priority patent/EA030187B1/en
Priority to CN202210260669.9A priority patent/CN114933585A/en
Priority to PL13733752T priority patent/PL2800743T3/en
Priority to KR1020147021897A priority patent/KR101893112B1/en
Priority to UAA201408870A priority patent/UA117451C2/en
Priority to CN202210634094.2A priority patent/CN115536635A/en
Priority to NZ627096A priority patent/NZ627096A/en
Priority to MX2014008350A priority patent/MX358940B/en
Priority to EP21194846.8A priority patent/EP3984997A1/en
Priority to EP13733752.3A priority patent/EP2800743B1/en
Publication of WO2013102431A1 publication Critical patent/WO2013102431A1/en
Priority to IL233503A priority patent/IL233503B/en
Priority to PH12014501561A priority patent/PH12014501561B1/en
Priority to ZA2014/05163A priority patent/ZA201405163B/en
Priority to CR20140377A priority patent/CR20140377A/en
Priority to HK15104396.5A priority patent/HK1203942A1/en
Priority to AU2017265096A priority patent/AU2017265096B9/en
Priority to HRP20180844TT priority patent/HRP20180844T1/en
Priority to CY20181100683T priority patent/CY1120506T1/en

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/53—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/5375—1,4-Oxazines, e.g. morpholine
    • A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
    • C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
    • C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D251/14—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom
    • C07D251/16—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to only one ring carbon atom
    • C07D251/18—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to only one ring carbon atom with nitrogen atoms directly attached to the two other ring carbon atoms, e.g. guanamines
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
    • C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
    • C07D493/08—Bridged systems

Definitions

  • Isocitrate dehydrogenases catalyze the oxidative decarboxylation of isocitrate to 2-oxoglutarate (i.e., a-ketoglutarate). These enzymes belong to two distinct subclasses, one of which utilizes NAD(+) as the electron acceptor and the other NADP(+).
  • NAD(+) the electron acceptor
  • NADP(+)-dependent isocitrate dehydrogenases Five isocitrate dehydrogenases have been reported: three NAD(+)-dependent isocitrate dehydrogenases, which localize to the mitochondrial matrix, and two NADP(+)-dependent isocitrate dehydrogenases, one of which is mitochondrial and the other predominantly cytosolic. Each NADP(+)-dependent isozyme is a homodimer.
  • IDH2 isocitrate dehydrogenase 2 (NADP+), mitochondrial
  • IDH isocitrate dehydrogenase 2 (NADP+), mitochondrial
  • IDP isocitrate dehydrogenase 2
  • IDHM isocitrate dehydrogenase 2
  • IDPM isocitrate dehydrogenase 2
  • ICD-M isocitrate dehydrogenase 2
  • mNADP-IDH mNADP-IDH.
  • NADP(+)-dependent isocitrate dehydrogenase found in the mitochondria. It plays a role in intermediary metabolism and energy production. This protein may tightly associate or interact with the pyruvate dehydrogenase complex.
  • Human IDH2 gene encodes a protein of 452 amino acids. The nucleotide and amino acid sequences for IDH2 can be found as GenBank entries NM_002168.2 and NP_002159.2 respectively. The nucleotide and amino acid sequence for human IDH2 are also described in, e.g., Huh et al., Submitted (NOV-1992) to the
  • Non-mutant e.g., wild type, IDH2 catalyzes the oxidative decarboxylation of isocitrate to a-ketoglutarate (a- KG) thereby reducing NAD + (NADP + ) to NADH (NADPH), e.g., in the forward reaction:
  • ring A is an optionally substituted 5-6 member monocyclic aryl or monocyclic heteroaryl
  • ring B is an optionally substituted 5-6 member monocyclic aryl or monocyclic heteroaryl
  • R and R J are each independently selected from hydrogen, C C 4 alkyl, C C 4 haloalkyl, -0-Ci-C4 alkyl, and CN, wherein any alkyl portion of R 1 is optionally substituted with -OH, NH 2 , NH(Ci-C 4 alkyl), or N(C C 4 alkyl) 2 ;
  • R is selected from: -(C -C alkyl), -(C 2 -C 6 alkenyl or alkynyl), -(C -C
  • any alkyl or alkylene moiety present in R is optionally substituted with one or more -OH, -0(Ci-C 4 alkyl) or halo;
  • any terminal methyl moiety present in R is optionally replaced with -CH 2 OH,
  • each R 6 is independently selected from hydrogen and CrC 6 alkyl
  • Q is selected from aryl, heteroaryl, carbocyclyl and heterocyclyl, any of which is optionally substituted; or
  • R 1 and R 2" are optionally taken together to form substituted carbocyclyl, optionally substituted heterocyclyl or optionally substituted heteroaryl, wherein:
  • -NH-C ⁇ XR 2 ) ⁇ 3 is not -NH(CH 2 )C(0)NH 2 ; d. when ring A is phenyl substituted with 2 or more hydroxyl or methoxy, and ring B is optionally substituted phenyl; then the portion of the compound represented by -NH-C ⁇ XR 2 ) ⁇ 3 ) is not -NH-cycloheptyl;
  • R 1 and R 3 do not form 2,2,6, 6,-tetramethylpiperidin-4-yl
  • each R a is hydrogen, CrC 4 alkyl or two R a s are taken together with the nitrogen to which they are commonly bound to form morpholin-4-yl or pipieridin-l-yl;
  • the compound is other than: (E)-3-(4-((4-((3-(diethylamino)propyl)amino)-6-phenyl-l,3,5-triazin-2-yl)amino)-2- methoxyphenyl)-2-phenylacrylonitrile ,
  • the compound of Formula I or II or as decribed in any one of the embodiments herein inhibits mutant IDH2, particularly mutant IDH2 having alpha hydroxyl neoactivity.
  • pharmaceutical compositions comprising a compound of Formula I and methods of using such compositions to treat cancers characterized by the presence of a mutant IDH2.
  • halo or halogen refers to any radical of fluorine, chlorine, bromine or iodine.
  • alkyl refers to a fully saturated or unsaturated hydrocarbon chain that may be a straight chain or branched chain, containing the indicated number of carbon atoms.
  • CrC 12 alkyl indicates that the group may have from 1 to 12 (inclusive) carbon atoms in it.
  • haloalkyl refers to an alkyl in which one or more hydrogen atoms are replaced by halo, and includes alkyl moieties in which all hydrogens have been replaced by halo (e.g., perfluoroalkyl).
  • arylalkyl or “aralkyl” refer to an alkyl moiety in which an alkyl hydrogen atom is replaced by an aryl group.
  • Aralkyl includes groups in which more than one hydrogen atom has been replaced by an aryl group.
  • arylalkyl or “aralkyl” include benzyl, 2-phenylethyl, 3-phenylpropyl, 9-fluorenyl, benzhydryl, and trityl groups.
  • alkyl includes "alkenyl” and "alkynyl”.
  • alkylene refers to a divalent alkyl, e.g., -CH 2 -, -CH 2 CH 2 -, -CH 2 CH 2 CH 2 - and -CH 2 CH(CH 3 )CH 2 -.
  • alkenyl refers to a straight or branched hydrocarbon chain containing 2-12 carbon atoms and having one or more double bonds.
  • alkenyl groups include, but are not limited to, allyl, propenyl, 2-butenyl, 3-hexenyl and 3-octenyl groups.
  • One of the double bond carbons may optionally be the point of attachment of the alkenyl substituent.
  • alkynyl refers to a straight or branched hydrocarbon chain containing 2-12 carbon atoms and characterized in having one or more triple bonds.
  • alkynyl groups include, but are not limited to, ethynyl, propargyl, and 3-hexynyl.
  • One of the triple bond carbons may optionally be the point of attachment of the alkynyl substituent.
  • alkoxy refers to an -O-alkyl radical.
  • haloalkoxy refers to an alkoxy in which one or more hydrogen atoms are replaced by halo, and includes alkoxy moieties in which all hydrogens have been replaced by halo (e.g., perfluoroalkoxy).
  • aryl refers to a fully aromatic monocyclic, bicyclic, or tricyclic hydrocarbon ring system. Examples of aryl moieties are phenyl, naphthyl, and anthracenyl. Unless otherwise specified, any ring atom in an aryl can be substituted by one or more substituents.
  • monocyclic aryl means a monocyclic fully romatic
  • hydrocarbon ring system optionally substituted by one or more substituents which can not form a fused bicyclic or tricyclic ring.
  • Carbocyclyl refers to a non-aromatic, monocyclic, bicyclic, or tricyclic hydrocarbon ring system.
  • Carbocyclyl groups include fully saturated ring systems (e.g., cycloalkyls), and partially saturated ring systems.
  • cycloalkyl as employed herein includes saturated cyclic, bicyclic, tricyclic, or polycyclic hydrocarbon groups having 3 to 12 carbons. Any ring atom can be substituted (e.g., by one or more substituents). Examples of cycloalkyl moieties include, but are not limited to, cyclopropyl, cyclohexyl, methylcyclohexyl, adamantyl, and norbornyl.
  • heteroaryl refers to a fully aromatic 5-8 membered monocyclic, 8-12 membered bicyclic, or 11-14 membered tricyclic ring system having 1-3 heteroatoms if monocyclic, 1-6 heteroatoms if bicyclic, or 1-9 heteroatoms if tricyclic, said heteroatoms selected from O, N, or S (or the oxidized forms such as N + -0 " , S(O) and S(0) 2 ).
  • monocyclic heteroaryl means a monocyclic fully romatic ring system having 1-3 heteroatoms, optionally substituted by one or more substituents which can not form a fused bicyclic or tricyclic ring.
  • heterocyclyl refers to a nonaromatic, 3-10 membered monocyclic, 8-12 membered bicyclic, or 11-14 membered tricyclic ring system having 1-3 heteroatoms if monocyclic, 1-6 heteroatoms if bicyclic, or 1-9 heteroatoms if tricyclic, said heteroatoms selected from O, N, or S (or the oxidized forms such as N + -0 " , S(O) and S(0) 2 ).
  • the heteroatom may optionally be the point of attachment of the heterocyclyl substituent.
  • heterocyclyl examples include, but are not limited to, tetrahydrofuranyl, tetrahydropyranyl, piperidinyl, morpholino, pyrrolinyl, pyrimidinyl, and pyrrolidinyl.
  • Heterocyclyl groups include fully saturated ring systems, and partially saturated ring systems.
  • Bicyclic and tricyclic ring systems containing one or more heteroatoms and both aromatic and non-aromatic rings are considered to be heterocyclyl or heteroaryl groups.
  • Bicyclic or tricyclic ring systems where an aryl or a heteroaryl is fused to a carbocyclyl or heterocyclyl and the point of attachment from the ring system to the rest of the molecule is through an aromatic ring are considered to be aryl or heteroaryl groups, respectively
  • Bicyclic or tricyclic ring systems where an aryl or a heteroaryl is fused to a carbocyclyl or heterocyclyl and the point of attachment from the ring system to the rest of the molecule is through the non-aromatic ring are considered to be carbocyclyl (e.g., cycloalkyl) or heterocyclyl groups, respectively.
  • any alkyl substituent is optionally further substituted with one or more of -OH, -0-(Ci-C 4 alkyl), halo, -NH 2 , -NH(Ci-C 4 alkyl), or -N(C C 4 alkyl) 2 ;
  • each R b is independently selected from hydrogen, and -Q-C 4 alkyl; or two R b s are taken together with the nitrogen atom to which they are bound to form a 4- to 8-membered heterocyclyl optionally comprising one additional heteroatom selected from N, S, and O; and
  • each R b is independently selected from C3-C7 carbocyclyl, phenyl, heteroaryl, and heterocyclyl, wherein one or more substitutable positions on said phenyl, cycloalkyl, heteroaryl or heterocycle substituent is optionally further substituted with one or more of -(Q-C 4 alkyl), -(C C 4 fluoroalkyl), -OH, -0-(C C 4 alkyl), -0-(C C 4 fluoroalkyl), halo, -NH 2 ,
  • Heterocyclyl groups are optionally substituted on one or more any substitutable nitrogen atom with oxo, -Q-C 4 alkyl, or fluoro-substituted Q-C 4 alkyl.
  • the term “substituted” refers to the replacement of a hydrogen atom by another group.
  • the term “elevated levels of 2HG” means 10%, 20% 30%, 50%, 75%, 100%, 200%, 500% or more 2HG then is present in a subject that does not carry a mutant IDH2 allele.
  • the term “elevated levels of 2HG” may refer to the amount of 2HG within a cell, within a tumor, within an organ comprising a tumor, or within a bodily fluid.
  • the term "bodily fluid” includes one or more of amniotic fluid surrounding a fetus, aqueous humour, blood (e.g., blood plasma), serum, Cerebrospinal fluid, cerumen, chyme, Cowper's fluid, female ejaculate, interstitial fluid, lymph, breast milk, mucus (e.g., nasal drainage or phlegm), pleural fluid, pus, saliva, sebum, semen, serum, sweat, tears, urine, vaginal secretion, or vomit.
  • blood e.g., blood plasma
  • serum Cerebrospinal fluid
  • cerumen cerumen
  • chyme chyme
  • Cowper's fluid female ejaculate
  • interstitial fluid lymph
  • breast milk mucus (e.g., nasal drainage or phlegm)
  • mucus e.g., nasal drainage or phlegm
  • pleural fluid pus, saliva, sebum, semen, serum
  • inhibitor or “prevent” include both complete and partial inhibition and prevention.
  • An inhibitor may completely or partially inhibit the intended target.
  • treat means decrease, suppress, attenuate, diminish, arrest, or stabilize the development or progression of a disease/disorder (e.g., a cancer), lessen the severity of the disease/disorder (e.g., a cancer) or improve the symptoms associated with the disease/disorder (e.g., a cancer).
  • a disease/disorder e.g., a cancer
  • lessen the severity of the disease/disorder e.g., a cancer
  • improve the symptoms associated with the disease/disorder e.g., a cancer
  • an amount of a compound effective to treat a disorder or a
  • terapéuticaally effective amount refers to an amount of the compound which is effective, upon single or multiple dose administration to a subject, in treating a cell, or in curing, alleviating, relieving or improving a subject with a disorder beyond that expected in the absence of such treatment.
  • the term "subject” is intended to include human and non-human animals.
  • exemplary human subjects include a human patient (referred to as a patient) having a disorder, e.g., a disorder described herein or a normal subject.
  • a disorder e.g., a disorder described herein or a normal subject.
  • non-human animals of one aspect of the invention includes all vertebrates, e.g., non-mammals (such as chickens, amphibians, reptiles) and mammals, such as non-human primates, domesticated and/or agriculturally useful animals, e.g., sheep, dog, cat, cow, pig, etc.
  • ring A is an optionally substituted 5-6 member monocyclic aryl or monocyclic heteroaryl
  • ring B is an optionally substituted 5-6 member monocyclic aryl or monocyclic heteroaryl
  • R 1 and R 3 J are each independently selected from hydrogen, CrC 4 alkyl, CrC 4 haloalkyl, -0-Ci-C 4 alkyl, and CN, wherein any alkyl portion of R 1 is optionally substituted with -OH, NH 2 , NH(Ci-C 4 alkyl), or N(Ci-C 4 alkyl) 2 ;
  • R is selected from: -(CrC 6 alkyl), -(C 2 -C 6 alkenyl or alkynyl), -(CrC 6
  • alkylene 0-(C 1 -C 6 alkylene)-Q, -(Ci-C 6 alkylene)-0-C(0)-(C 1 -C 6 alkyl), -(Ci-C 6
  • any terminal methyl moiety present in R is optionally replaced with -CH 2 OH, CF 3 ,
  • each R 6 is independently selected from hydrogen and C]_-C alkyl
  • Q is selected from aryl, heteroaryl, carbocyclyl and heterocyclyl; and Q is optionally substituted; or
  • R and R" are optionally taken together to form an optionally substituted carbocyclyl, optionally substituted heterocyclyl or optionally substituted heteroaryl; wherein:
  • compound represented by -NH-C(R )(R )(R ) is not cysteine, optionally substituted phenylalanine or leucine or methyl ester thereof;
  • each R a is hydrogen, C C 4 alkyl or two R a s are taken together with the nitrogen to which they are commonly bound to form morpholin-4-yl or pipieridin-l-yl;
  • ring A when ring A is unsubstituted phenyl and the portion of the compound represented by -NHC ⁇ XR 2 ) ⁇ 3 ) is -NH-CH 2 CH 2 N(CH 3 ) 2 , -NH-CH 2 CH 2 -morpholin-4-yl or -NH-CH 2 CH 2 OH; then ring B is other than oxadiazole, imidazole, thiazole or oxazole each of which is substituted with -C(0)NHR b , wherein R b is isopropyl, cyclopropyl or 2-chloro-6-methylphenyl;
  • ring A is an optionally substituted 5-6 member monocyclic aryl or monocyclic heteroaryl
  • ring B is an optionally substituted 5-6 member monocyclic aryl or monocyclic heteroaryl
  • R is selected from: -(C -C alkyl), -(C 2 -C 6 alkenyl or alkynyl), -(C -C alkylene)-N(R 6 )-(C 1 -C 6 alkylene)-0-(C 1 -C 6 alkyl), -(Ci-C 6 alkylene)-N(R 6 )-(C 0 -C 6 alkylene)-Q, -(Ci-C 6 alkylene)-N(R 6 )(R 6 ), -(Ci-Ce alkylene)-N(R 6 )-S(0) 1 _ 2 -(C 1 -C 6 alkyl), -(d-C 6 alkylene)-N(R 6 )-S(O) 1 _ 2 -(C 0 -C 6 alkyl)-Q, -(d-C 6 alkylene)-S(0) 1 _ 2 -N(R 6 )(R 6 ), -
  • any alkyl or alkylene moiety present in R is optionally substituted with one or more -OH, -0(Ci-C 4 alkyl) or halo;
  • each R 6 is independently selected from hydrogen and C]_-C alkyl
  • Q is selected from aryl, heteroaryl, carbocyclyl and heterocyclyl, any of which is optionally substituted; or
  • R and R" are optionally taken together to form substituted carbocyclyl or optionally substituted heterocyclyl, wherein:
  • -NH-C ⁇ XR 2 ) ⁇ 3 is not -NH(CH 2 )C(0)NH 2 ; d. when ring A is phenyl substituted with 2 or more hydroxyl or methoxy, and ring B is optionally substituted phenyl; then the portion of the compound represented by -NH-C ⁇ XR 2 ) ⁇ 3 ) is not -NH-cycloheptyl;
  • ring A when ring A is unsubstituted phenyl and the portion of the compound represented by -NHC(R 1 )(R 2 )(R 3 ) is -NH-CH 2 CH 2 N(CH 3 ) 2 , -NH-CH 2 CH 2 -morpholin-4-yl or -NH-CH 2 CH 2 OH; then ring B is other than oxadiazole, thiazole or oxazole each of which is substituted with -C(0)NHR b , wherein R b is isopropyl, cyclopropyl or 2-chloro-6-methylphenyl;
  • R 1 is independently selected from hydrogen, -CH 3 ,
  • R 1 and R 2 are taken together to form carbocyclyl or heterocyclyl, either of which is optionally substituted with up to 3 substituents independently selected from halo.
  • Ci-C 4 alkyl, C1-C4 haloalkyl, C1-C4 alkoxy, -CN, 0, -OH, and -C(0)Ci-C 4 alkyl.
  • Q is selected from pyridinyl,
  • R 1 and R 2 are taken together to form cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, tetrahydrofuranyl, tetrahydropyranyl, oxetanyl, bicyclo[2.2.1]heptanyl, oxobicyclo[3.1.0]hexanyl, azetidinyl, phenyl and pyridinyl, any of which is optionally substituted with up to 2 substituents independently selected from Q-C 4 alkyl, Q-C 4 alkoxy, C 3 -C 6 cycloalkyl, -OH, -C(0)CH 3 , fluoro, and chloro.
  • ring A is an optionally substituted 6-membered monocyclic aryl. In some embodiments, ring A is an optionally substituted 5-6 membered heteroaryl. In some embodiments, ring A is an optionally substituted 6 membered heteroaryl.
  • ring A is selected from phenyl, pyrazolyl, oxazolyl, isoxazolyl, pyridinyl, pyrimidinyl, pyrazinyl, and thiazolyl, wherein ring A is optionally substituted with up to two substituents independently selected from halo, -CrC 4 alkyl, -CrC 4 haloalkyl, -CrC 4 hydroxyalkyl, -NH-S(0) 2 -(Ci-C 4 alkyl), -S(0) 2 NH(Ci-C 4 alkyl), -CN, -S(0) 2 -(Ci-C 4 alkyl), C 1 -C4 alkoxy, -NH(Ci-C 4 alkyl), -OH, -OCF 3 , -CN, -NH 2 , -C(0)NH 2 , -C(0)NH(Ci-C 4 alkyl), -C(0)-N(C
  • ring A is selected from phenyl, pyrazolyl, oxazolyl, isoxazolyl, pyridinyl, pyrimidinyl, pyrazinyl, and thiazolyl, wherein ring A is optionally substituted with up to two substituents independently selected from halo, -C 1 -C 4 alkyl, -C 1 -C 4 haloalkyl, -C 1 -C 4 hydroxyalkyl, -NH-S(0) 2 -(Ci-C 4 alkyl), -S(0) 2 NH(Ci-C 4 alkyl), -CN, -S(0) 2 -(Ci-C 4 alkyl), CrC 4 alkoxy, -NH(C C 4 alkyl), -OH, -CN, and -NH 2 .
  • ring B is selected from phenyl, pyrazolyl, oxazolyl, isoxazolyl, thiazolyl, pyridinyl, pyrimidinyl, pyridazinyl, and pyrazinyl, wherein ring B is optionally substituted with up to two substituents independently selected from halo, -C 1 -C 4 alkyl, -C 2 -C 4 alkynyl, -CrC 4 haloalkyl, -CrC 4 hydroxyalkyl, C 3 -C 6 cycloalkyl, -(C 0 -C 2 alkylene)-0-C 1 -C 4 alkyl, -0-(CrC 4 alkylene)-C 3 -C 6 cycloalkyl, -NH-S(0) 2 -(Ci-C 4 alkyl), -S(0) 2 NH(Ci-C 4 alkyl), -S(0) 2 NH(Ci
  • Ring A' is selected from phenyl and pyridin-2-yl, wherein ring A' is optionally substituted with one or two substituents independently selected from chloro, fluoro, -CF , -CHF 2 , -CH 3 , -CH 2 CH 3 , -CF 2 CH 3 , -OH, -OCH 3 , -OCH 2 CH 3 , -NH 2 , -NH(CH 3 ), and -N(CH 3 ) 2 ;
  • Ring B' is selected from pyridin-3-yl, pyridin-4-yl, isoxazoly-4-yl, isoxazol-3-yl, thiazol-5-yl, pyrimidin-5-yl and pyrazol-4-yl, wherein ring B' is optionally substituted with one to two substituents independently selected from halo; -CN; -OH; CrC 4 alkyl optionally substituted with halo, CN or -OH; -S(0) 2 -Ci-C 4 alkyl; -S(0)-Ci-C 4 alkyl; -S(0) 2 -NH-Ci-C 4 alkyl; -S(0) 2 -N(Ci-C 4 alkyl) 2 ; -S(0) 2 -azetidin-l-yl; -O-C1-C4 alkyl; -CH 2 -0-CH 3 ,
  • -C(R la )(R 2a )(R 3a ) is selected from Ci-C 6 alkyl optionally substituted with halo or -OH; -(Co-Ci alkylene)-cycloalkyl, wherein the alkylene is optionally substituted with methyl and the cycloalkyl is optionally substituted with halo, -OCH 3 or methyl; saturated heterocyclyl optionally substituted with halo or methyl; -C(0)-0-C 1 -C6 alkyl; -C(0)-(Co-C 1 alkylene)-cyclopropyl; and C(0)-benzyl.
  • ring A' is selected from 2-chlorophenyl, 2- fluorophenyl, 2-methoxyphenyl, 3-hydroxyphenyl, 6-aminopyridin-2-yl, 6-chloropyridin-2-yl, 6- trifluoromethylpyridin-2-yl, and phenyl.
  • ring B' is selected from 2-(morpholin-4- yl)pyridin-4-yl, 2-dimethylaminopyridin-4-yl, 3-(2-methyoxyethyl)phenyl, 3,5-difluorophenyl,
  • the moiety represented by C(R la )(R 2a )(R 3a ) is selected from 2-hydroxycyclopentyl, 3-hydroxycyclopentyl, 1-methylcyclopropyl, 2- methylcyclopropyl, 3,3-difluorocyclobutyl, bicycloheptanyl, -(CH 2 ) CH , -CH(CH )-C(CH ) , -CH(CH 3 )-CH 2 OCH 3 , -C(0)-C(CH 3 ) 3 , -C(0)-OC(CH 3 ) 3 , -C(0)CH 2 OH, -C(0)-CH(CH 3 ) 2 , -C(0)-l-hydroxycyclopropyl, -C(0)-2-pyrrolidinon-5-yl, -C(0)-2-pyrrolyl,
  • the moiety represented by C(R la )(R 2a )(R 3a ) is selected from 2-hydroxycyclopentyl, 2-methylcyclopropyl, 3,3-difluorocyclobutyl,
  • Ring A' is selected from phenyl, pyrimidin-2-yl, pyrimidin-4-yl, pyrimidin-5-yl, oxazol-
  • Ring B' is selected from phenyl, pyridin-3-yl, pyridin-4-yl, pyridazin-4-yl, isoxazol-4-yl, isoxazol-3-yl, thiazol-5-yl, pyrimidin-5-yl and pyrazol-4-yl, wherein ring B' is optionally substituted with one to two substituents independently selected from halo; -CN; -OH; C C 4 alkyl optionally substituted with halo, CN or -OH; -S(0) 2 -Ci-C 4 alkyl; -S(0)-Ci-C 4 alkyl;
  • cyclopropyl-C 1 -C 4 alkoxy cyclopropyl-CN, -S(0) 2 -NH-cyclopropyl; -S(0) 2 -NH-CH 2 - cyclopropyl; -C(0)-Ci-C 4 alkyl, -C(0)-0-CH 3 ; and
  • -C(R la )(R 2a )(R 3a ) is selected from Ci-C 6 alkyl optionally substituted with halo, -OCH 3 , -P(0) 3 " or -OH; -(Co-Q alkylene)-cycloalkyl, wherein the alkylene is optionally substituted with methyl and the cycloalkyl is optionally substituted with -OH, -CH 2 OH, halo, -OCH or methyl; saturated or partially saturated -(Co-Ci alkylene) -heterocyclyl wherein the heterocyclyl is optionally substituted with halo, -S(0) 2 -CH 2 -C(0)-Ci-C 6 alkyl, -S(0) 2 -Ci-C 6 alkyl, -C(0)-0-Ci- C 6 alkyl, -C(0)-N(CH 3 ) 2 or methyl; -C(0)-0-Ci-C 6 alkyl; -C(
  • ring A' is selected from 2-chlorophenyl, 2- fluorophenyl, 2-methoxyphenyl, 3-hydroxyphenyl, 3-amidophenyl, 3-methylsulfinylphenyl, 3- methylsulfonylphenyl, 3-(l-methanol)phenyl, 3-methanaminephenyl, 3-methoxy-2-fluorophenyl,
  • 6- aminopyridin-2-yl 4-fluoro-6-aminopyridin-2-yl, 6-propen-l-ylpyridin-2-yl, 6-prop-l- ylpyridin-2-yl, 6-methylaminopyridin-2-yl, 3-fluoro-6-trifluoromethylpyridin-2-yl, 4-chloro-6- aminopyridin-2-yl, 4-fluoro-6-aminopyridin-2-yl, 4-chloro-6-methoxypyridin-2-yl, 6- aminopyridin-3-yl, 2-methoxypyridin-3-yl, 6-aminopyridin-2-yl, 6-chloropyridin-2-yl, 6- trifluoromethylpyridin-2-yl, 6-difluoromethylpyridin-2-yl, 4-(CH 2 OH)-6-trifluoromethyl- pyridin-2-yl, 4-(CH 2 OH)-6-chloro-pyridin
  • ring B' is selected from 2-(morpholin-4- yl)pyridin-4-yl, 2-dimethylaminopyridin-4-yl, 3-(2-methyoxyethyl)phenyl, 3,5-difluorophenyl, 3-chlorophenyl, 3-cyanomethylphenyl, 3-cyanophenyl, 3-(cyclopropylmethyl)phenyl, 3- cyclopropylaminosulfonylphenyl, 3-dimethylaminosulfonylphenyl, 3-ethylsulfonylphenyl, 3- fhiorophenyl, 3-methylsulfonylphenyl, 4-fluorophenyl, 3-(l-hydroxyisopropyl)phenyl, 3- methylsulfonyl-5-chlorophenyl, 3-methylsulfonyl-5-fluorophenyl, 3-(N-2,2,2,- trifluoroethy
  • the moiety represented by C(R la )(R 2a )(R 3a ) is selected from 2-hydroxycyclopentyl, 3-hydroxycyclopentyl, 1-methylcyclopropyl, 2- methylcyclopropyl, 3,3-difluorocyclobutyl, bicycloheptanyl, -(CH 2 ) 3 CH 3 , -CH(CH 3 )-C(CH 3 )3, -CH(CH 3 )-CH 2 OCH 3 , -C(0)-C(CH 3 ) 3 , -C(0)-OC(CH 3 ) 3 , -C(0)CH 2 OH, -C(0)-CH(CH 3 ) 2 , -C(0)-l-hydroxycyclopropyl, -C(0)-2-pyrrolidinon-5-yl, -C(0)-2-pyrrolyl,
  • the moiety represented by C(R la )(R 2a )(R 3a ) is selected from 2-hydroxycyclopentyl, 2-methylcyclopropyl, 3,3-difluorocyclobutyl, bicycloheptanyl, -(CH 2 ) 3 CH 3 , -CH(CH 3 )-C(CH 3 ) 3 , -CH(CH 3 )-CH 2 OCH 3 , -C(0)-C(CH 3 ) 3 , -C(0)-CH(CH 3 ) 2 , -C(0)-cyclopropyl, -C(0)-OC(CH 3 ) 3 , -C(0)-OCH 2 CH(CH 3 ) 2 ,
  • the moiety represented by C(R la )(R 2a )(R 3a ) is selected from 2-methylcyclopropyl, -(CH 2 ) 3 CH 3 , -CH(CH 3 )-C(CH 3 ) 3 , -CH(CH 3 )-CH 2 OCH 3 , -CH(CH 3 )-CH(CH 3 ) 2 , -CH(CH 3 )-CH 2 CH 3 , -CH 2 C(CH 3 ) 2 -CH 2 OH, -CH 2 C(OH)(CH 3 ) 3 , CH 2 C(CH 3 ) 3 , -CH 2 CF 3 , -CH 2 CH(CH 3 ) 2 , -CH(CH 3 ) 2 , -CH 2 CH(CH 3 )-CH 2 CH 3 ,
  • the compound is selected from any one of the compounds set forth in Table 1, below.
  • step (2) reacting .
  • the preceding methods comprise ; step (2) reacting tep (3) reacting
  • omprise step (1) reacting
  • step (1) reacting
  • step (2) reacting
  • the preceding methods comprise step (1) reacting
  • the preceding methods comprise step (1) reacting
  • the preceding methods comprise step (1) reacting
  • step (2) reacting w ith .
  • the preceding methods the preceding methods
  • step (1) converting to ; step (2) reacting
  • the compounds of one aspect of this invention may contain one or more asymmetric centers and thus occur as racemates, racemic mixtures, scalemic mixtures, and diastereomeric mixtures, as well as single enantiomers or individual stereoisomers that are substantially free from another possible enantiomer or stereoisomer.
  • substantially free of other stereoisomers means a preparation enriched in a compound having a selected stereochemistry at one or more selected stereocenters by at least about 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98%, or 99%.
  • enriched means that at least the designated percentage of a preparation is the compound having a selected stereochemistry at one or more selected stereocenters.
  • the compound of Formula I or II is enriched for a structure or structures having a selected stereochemistry at one or more carbon atoms.
  • the compound is enriched in the specific stereoisomer by at least about 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98%, or 99%.
  • the compounds of Formula I or II may also comprise one or more isotopic substitutions.
  • H may be in any isotopic form, including H, H (D or deuterium), and H (T or tritium); C may be in any isotopic form, including 12 C, 13 C, and 14 C; O may be in any isotopic form, including 16 0 and 18 0; and the like.
  • the compound is enriched in a specific isotopic form of H, C and/or O by at least about 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98%, or 99%.
  • the compounds of one aspect of this invention may also be represented in multiple tautomeric forms, in such instances, one aspect of the invention expressly includes all tautomeric forms of the compounds described herein, even though only a single tautomeric form may be represented (e.g., alkylation of a ring system may result in alkylation at multiple sites, one aspect of the invention expressly includes all such reaction products; and keto-enol tautomers). All such isomeric forms of such compounds are expressly included herein.
  • a corresponding salt of the active compound for example, a pharmaceutically-acceptable salt.
  • a salt may be formed with a suitable cation.
  • suitable inorganic cations include, but are not limited to, alkali metal ions such as Na + and K + , alkaline earth cations such as Ca 2+ and Mg 2+ , and other cations such as Al 3+ .
  • Suitable organic cations include, but are not limited to, ammonium ion (i.e., NH 4 + ) and substituted ammonium ions ⁇ e.g., NH 3 R + , NH 2 R 2+ , NHR 3+ , NR 4+ ).
  • suitable substituted ammonium ions are those derived from: ethylamine, diethylamine,
  • dicyclohexylamine triethylamine, butylamine, ethylenediamine, ethanolamine, diethanolamine, piperazine, benzylamine, phenylbenzylamine, choline, meglumine, and tromethamine, as well as amino acids, such as lysine and arginine.
  • An example of a common quaternary ammonium ion is N(CH 3 ) 4 + .
  • a salt may be formed with a suitable anion.
  • suitable inorganic anions include, but are not limited to, those derived from the following inorganic acids:
  • hydrochloric hydrobromic, hydroiodic, sulfuric, sulfurous, nitric, nitrous, phosphoric, and phosphorous.
  • Suitable organic anions include, but are not limited to, those derived from the following organic acids: 2-acetyoxybenzoic, acetic, ascorbic, aspartic, benzoic,
  • glucoheptonic, gluconic, glutamic glycolic, hydroxymaleic, hydroxynaphthalene carboxylic, isethionic, lactic, lactobionic, lauric, maleic, malic, methanesulfonic, mucic, oleic, oxalic, palmitic, pamoic, pantothenic, phenylacetic, phenylsulfonic, propionic, pyruvic, salicylic, stearic, succinic, sulfanilic, tartaric, toluenesulfonic, and valeric.
  • Mesylates of each compound in Table 1 are explicitly included herein.
  • suitable polymeric organic anions include, but are not limited to, those derived from the following polymeric acids: tannic acid, carboxymethyl cellulose.
  • prodrugs examples include esters (e.g., phosphates, amino acid (e.g., valine) esters), carbamates and other pharmaceutically acceptable derivatives, which, upon administration to a subject, are capable of providing active compounds.
  • esters e.g., phosphates, amino acid (e.g., valine) esters
  • carbamates e.g., benzyl alcohol, benzyl ether, benzyl ether ether, sulfonate, sodium phosphates, sodium phosphates of each compound in Table 1, if applicable, are explicitly included herein.
  • Amino acid (e.g., valine) esters of each compound in Table 1, if applicable, are explicitly included herein.
  • compositions and routes of administration are provided.
  • compositions may be formulated together with a pharmaceutically acceptable carrier or adjuvant into pharmaceutically acceptable compositions prior to be administered to a subject.
  • pharmaceutically acceptable compositions further comprise additional therapeutic agents in amounts effective for achieving a modulation of disease or disease symptoms, including those described herein.
  • pharmaceutically acceptable carrier or adjuvant refers to a carrier or adjuvant that may be administered to a subject, together with a compound of one aspect of this invention, and which does not destroy the pharmacological activity thereof and is nontoxic when administered in doses sufficient to deliver a therapeutic amount of the compound.
  • Cyclodextrins such as ⁇ -, ⁇ -, and ⁇ -cyclodextrin, or chemically modified derivatives such as hydroxyalkylcyclodextrins, including 2- and
  • compositions of one aspect of this invention may be administered orally, parenterally, by inhalation spray, topically, rectally, nasally, buccally, vaginally or via an implanted reservoir, preferably by oral administration or administration by injection.
  • the pharmaceutical compositions of one aspect of this invention may contain any conventional non-toxic pharmaceutically-acceptable carriers, adjuvants or vehicles.
  • the pH of the formulation may be adjusted with pharmaceutically acceptable acids, bases or buffers to enhance the stability of the formulated compound or its delivery form.
  • parenteral as used herein includes subcutaneous, intracutaneous, intravenous, intramuscular, intraarticular, intraarterial, intrasynovial, intrasternal, intrathecal, intralesional and intracranial injection or infusion techniques.
  • the pharmaceutical compositions may be in the form of a sterile injectable preparation, for example, as a sterile injectable aqueous or oleaginous suspension.
  • This suspension may be formulated according to techniques known in the art using suitable dispersing or wetting agents (such as, for example, Tween 80) and suspending agents.
  • the sterile injectable preparation may also be a sterile injectable solution or suspension in a non-toxic parenterally acceptable diluent or solvent, for example, as a solution in 1,3-butanediol.
  • suitable vehicles and solvents that may be employed are mannitol, water, Ringer's solution and isotonic sodium chloride solution.
  • sterile, fixed oils are conventionally employed as a solvent or suspending medium.
  • any bland fixed oil may be employed including synthetic mono- or diglycerides.
  • Fatty acids, such as oleic acid and its glyceride derivatives are useful in the preparation of injectables, as are natural pharmaceutically-acceptable oils, such as olive oil or castor oil, especially in their polyoxyethylated versions.
  • These oil solutions or suspensions may also contain a long-chain alcohol diluent or dispersant, or carboxymethyl cellulose or similar dispersing agents which are commonly used in the formulation of pharmaceutically acceptable dosage forms such as emulsions and or suspensions.
  • compositions of one aspect of this invention may be orally administered in any orally acceptable dosage form including, but not limited to, capsules, tablets, emulsions and aqueous suspensions, dispersions and solutions.
  • carriers which are commonly used include lactose and corn starch.
  • Lubricating agents such as magnesium stearate, are also typically added.
  • useful diluents include lactose and dried corn starch.
  • Topical administration of the pharmaceutical compositions of one aspect of this invention is useful when the desired treatment involves areas or organs readily accessible by topical application.
  • the pharmaceutical composition should be formulated with a suitable ointment containing the active components suspended or dissolved in a carrier.
  • Carriers for topical administration of the compounds of one aspect of this invention include, but are not limited to, mineral oil, liquid petroleum, white petroleum, propylene glycol, polyoxyethylene polyoxypropylene compound, emulsifying wax and water.
  • the pharmaceutical composition can be formulated with a suitable lotion or cream containing the active compound suspended or dissolved in a carrier with suitable emulsifying agents.
  • Suitable carriers include, but are not limited to, mineral oil, sorbitan monostearate, polysorbate 60, cetyl esters wax, cetearyl alcohol, 2-octyldodecanol, benzyl alcohol and water.
  • the pharmaceutical compositions of one aspect of this invention may also be topically applied to the lower intestinal tract by rectal suppository formulation or in a suitable enema formulation.
  • Topically-transdermal patches are also included in one aspect of this invention.
  • compositions of one aspect of this invention may be administered by nasal aerosol or inhalation.
  • Such compositions are prepared according to techniques well-known in the art of pharmaceutical formulation and may be prepared as solutions in saline, employing benzyl alcohol or other suitable preservatives, absorption promoters to enhance bioavailability, fluorocarbons, and/or other solubilizing or dispersing agents known in the art.
  • compositions of one aspect of this invention comprise a combination of a compound of the formulae described herein and one or more additional therapeutic or prophylactic agents
  • both the compound and the additional agent should be present at dosage levels of between about 1 to 100%, and more preferably between about 5 to 95% of the dosage normally administered in a monotherapy regimen.
  • the additional agents may be administered separately, as part of a multiple dose regimen, from the compounds of one aspect of this invention. Alternatively, those agents may be part of a single dosage form, mixed together with the compounds of one aspect of this invention in a single composition.
  • the compounds described herein can, for example, be administered by injection, intravenously, intraarterially, subdermally, intraperitoneally, intramuscularly, or subcutaneously; or orally, buccally, nasally, transmucosally, topically, in an ophthalmic preparation, or by inhalation, with a dosage ranging from about 0.5 to about 100 mg/kg of body weight, alternatively dosages between 1 mg and 1000 mg/dose, every 4 to 120 hours, or according to the requirements of the particular drug.
  • the methods herein contemplate administration of an effective amount of compound or compound composition to achieve the desired or stated effect.
  • the pharmaceutical compositions of one aspect of this invention will be administered from about 1 to about 6 times per day or alternatively, as a continuous infusion.
  • administration can be used as a chronic or acute therapy.
  • the amount of active ingredient that may be combined with the carrier materials to produce a single dosage form will vary depending upon the host treated and the particular mode of administration.
  • a typical preparation will contain from about 5% to about 95% active compound (w/w).
  • such preparations contain from about 20% to about 80% active compound.
  • the dosage or frequency of administration, or both may be reduced, as a function of the symptoms, to a level at which the improved condition is retained when the symptoms have been alleviated to the desired level.
  • Subjects may, however, require intermittent treatment on a long-term basis upon any recurrence of disease symptoms.
  • compositions described above comprising a compound of Structural Formula I or II or a compound described in any one of the embodiments herein, may further comprise another therapeutic agent useful for treating cancer.
  • IDH2R140Q and IDH2R172K The inhibitory activities of the compounds provided herein against IDH2 mutants (e.g., IDH2R140Q and IDH2R172K) can be tested by methods described in Example 12 or analogous methods.
  • the cancer to be treated is characterized by a mutant allele of IDH2 wherein the IDH2 mutation results in a new ability of the enzyme to catalyze the NAPH-dependent reduction of a-ketoglutarate to R(-)-2-hydroxyglutarate in a subject.
  • the mutant IDH2 has an R140X mutation.
  • the R140X mutation is a R140Q mutation.
  • the R140X mutation is a R140W mutation. In another aspect of this embodiment, the R140X mutation is a R140L mutation. In another aspect of this embodiment, the mutant IDH2 has an R172X mutation. In another aspect of this embodiment, the R172X mutation is a R172K mutation. In another aspect of this embodiment, the R172X mutation is a R172G mutation.
  • Also provided are methods of treating a cancer characterized by the presence of a mutant allele of IDH2 comprising the step of administering to subject in need thereof (a) a compound of Structural Formula I or II, a compound described in any one of the embodiments herein, or a pharmaceutically acceptable salt thereof, or (b) a pharmaceutical composition comprising (a) and a pharmaceutically acceptable carrier.
  • the cancer to be treated is characterized by a mutant allele of IDH2 wherein the IDH2 mutation results in a new ability of the enzyme to catalyze the
  • the mutant IDH2 has an R140X mutation.
  • the R140X mutation is a R140Q mutation.
  • the R140X mutation is a R140W mutation.
  • the R140X mutation is a R140L mutation.
  • the mutant IDH2 has an R172X mutation.
  • the R172X mutation is a R172K mutation.
  • the R172X mutation is a R172G mutation.
  • a cancer can be analyzed by sequencing cell samples to determine the presence and specific nature of (e.g., the changed amino acid present at) a mutation at amino acid 140 and/or 172 of IDH2.
  • mutant alleles of IDH2 wherein the IDH2 mutation results in a new ability of the enzyme to catalyze the NAPH-dependent reduction of a-ketoglutarate to R(-)-2-hydroxyglutarate, and in particular R140Q and/or R172K mutations of IDH2, characterize a subset of all types of cancers, without regard to their cellular nature or location in the body.
  • the compounds and methods of one aspect of this invention are useful to treat any type of cancer that is characterized by the presence of a mutant allele of IDH2 imparting such acitivity and in particular an IDH2 R140Q and/or R172K mutation.
  • the efficacy of cancer treatment is monitored by measuring the levels of 2HG in the subject. Typically levels of 2HG are measured prior to treatment, wherein an elevated level is indicated for the use of the compound of Formula I or II or a compound described in any one of the embodiments described herein to treat the cancer. Once the elevated levels are established, the level of 2HG is determined during the course of and/or following termination of treatment to establish efficacy. In certain embodiments, the level of 2HG is only determined during the course of and/or following termination of treatment. A reduction of 2HG levels during the course of treatment and following treatment is indicative of efficacy. Similarly, a determination that 2HG levels are not elevated during the course of or following treatment is also indicative of efficacy.
  • the these 2HG measurements will be utilized together with other well-known determinations of efficacy of cancer treatment, such as reduction in number and size of tumors and/or other cancer- associated lesions, improvement in the general health of the subject, and alterations in other biomarkers that are associated with cancer treatment efficacy.
  • 2HG can be detected in a sample by LC/MS.
  • the sample is mixed 80:20 with methanol, and centrifuged at 3,000 rpm for 20 minutes at 4 degrees Celsius.
  • the resulting supernatant can be collected and stored at -80 degrees Celsius prior to LC-MS/MS to assess 2-hydroxyglutarate levels.
  • LC liquid chromatography
  • Each method can be coupled by negative electrospray ionization (ESI, -3.0 kV) to triple-quadrupole mass spectrometers operating in multiple reaction monitoring (MRM) mode, with MS parameters optimized on infused metabolite standard solutions.
  • ESI, -3.0 kV negative electrospray ionization
  • MRM multiple reaction monitoring
  • Metabolites can be separated by reversed phase chromatography using 10 mM tributyl- amine as an ion pairing agent in the aqueous mobile phase, according to a variant of a previously reported method (Luo et al. J Chromatogr A 1147, 153-64, 2007).
  • Another method is specific for 2-hydroxyglutarate, running a fast linear gradient from 50% -95% B (buffers as defined above) over 5 minutes.
  • a Synergi Hydro-RP, 100mm x 2 mm, 2.1 ⁇ particle size (Phenomonex) can be used as the column, as described above.
  • Metabolites can be quantified by comparison of peak areas with pure metabolite standards at known concentration. Metabolite flux studies from 13 C-glutamine can be performed as described, e.g., in Munger et al. Nat Biotechnol 26, 1179-86, 2008.
  • 2HG is directly evaluated.
  • a derivative of 2HG formed in process of performing the analytic method is evaluated.
  • a derivative can be a derivative formed in MS analysis.
  • Derivatives can include a salt adduct, e.g., a Na adduct, a hydration variant, or a hydration variant which is also a salt adduct, e.g., a Na adduct, e.g., as formed in MS analysis.
  • a metabolic derivative of 2HG is evaluated.
  • examples include species that build up or are elevated, or reduced, as a result of the presence of 2HG, such as glutarate or glutamate that will be correlated to 2HG, e.g., R-2HG.
  • Exemplary 2HG derivatives include dehydrated derivatives such as the compounds provided below or a salt adduct thereof:
  • the cancer is a tumor wherein at least 30, 40, 50, 60, 70, 80 or 90% of the tumor cells carry an IDH2 mutation, and in particular an IDH2 R140Q, R140W, or R140L and/or R172K or R172G mutation, at the time of diagnosis or treatment.
  • one aspect of the invention provides a method of treating a cancer selected from glioblastoma (glioma), myelodysplastic syndrome (MDS),
  • myeloproliferative neoplasm MPN
  • acute myelogenous leukemia AML
  • sarcoma melanoma
  • non-small cell lung cancer chondrosarcoma
  • cholangiocarcinomas cholangiocarcinomas or angioimmunoblastic lymphoma
  • the cancer to be treated is glioma, myelodysplastic syndrome (MDS), myeloproliferative neoplasm (MPN), acute myelogenous leukemia (AML), melanoma, chondrosarcoma, or angioimmunoblastic non- Hodgkin's lymphoma (NHL).
  • MDS myelodysplastic syndrome
  • MPN myeloproliferative neoplasm
  • AML acute myelogenous leukemia
  • melanoma chondrosarcoma
  • NDL angioimmunoblastic non- Hodgkin's lymphoma
  • 2HG is known to accumulate in the inherited metabolic disorder 2-hydroxyglutaric aciduria. This disease is caused by deficiency in the enzyme 2-hydroxyglutarate dehydrogenase, which converts 2HG to a-KG (Struys, E. A. et al. Am J Hum Genet 76, 358-60 (2005)).
  • 2-hydroxyglutarate dehydrogenase deficiencies accumulate 2HG in the brain as assessed by MRI and CSF analysis, develop leukoencephalopathy, and have an increased risk of developing brain tumors (Aghili, M., Zahedi, F. & Rafiee, J Neurooncol 91, 233-6 (2009); Kolker, S., Mayatepek, E. & Hoffmann, G. F.
  • transaminases which allow utilization of glutamate nitrogen for amino and nucleic acid biosynthesis, and aKG-dependent prolyl hydroxylases such as those which regulate Hif 1-alpha levels.
  • one aspect of the invention provides a method of treating 2-hydroxyglutaric aciduria, particularly D-2-hydroxyglutaric aciduria, in a patient by administering to the patient a compound of Structural Formula I or II or a compound described in any one of the embodiments described herein.
  • Treatment methods described herein can additionally comprise various evaluation steps prior to and/or following treatment with a compound of Structural Formula I or II or a compound described in any one of the embodiments described herein.
  • the method further comprises the step of evaluating the growth, size, weight, invasiveness, stage and/or other phenotype of the cancer.
  • the method further comprises the step of evaluating the IDH2 genotype of the cancer. This may be achieved by ordinary methods in the art, such as DNA sequencing, immuno analysis, and/or evaluation of the presence, distribution or level of 2HG.
  • the method further comprises the step of determining the 2HG level in the subject.
  • This may be achieved by spectroscopic analysis, e.g., magnetic resonance-based analysis, e.g., MRI and/or MRS measurement, sample analysis of bodily fluid, such as serum or spinal cord fluid analysis, or by analysis of surgical material, e.g., by mass-spectroscopy.
  • the methods described herein comprise the additional step of co-administering to a subject in need thereof a second therapy e.g., an additional cancer therapeutic agent or an additional cancer treatment.
  • additional cancer therapeutic agents include for example, chemotherapy, targeted therapy, antibody therapies, immunotherapy, and hormonal therapy.
  • Additional cancer treatments include, for example: surgery, and radiation therapy. Examples of each of these treatments are provided below.
  • co-administering means that the additional cancer therapeutic agent may be administered together with a compound of one aspect of this invention as part of a single dosage form (such as a composition of one aspect of this invention comprising a compound of one aspect of the invention and an second therapeutic agent as described above) or as separate, multiple dosage forms.
  • the additional cancer therapeutic agent may be administered prior to, consecutively with, or following the administration of a compound of one aspect of this invention.
  • both the compounds of one aspect of this invention and the second therapeutic agent(s) are administered by conventional methods.
  • compositions of one aspect of this invention comprising both a compound of one aspect of the invention and a second therapeutic agent, to a subject does not preclude the separate administration of that same therapeutic agent, any other second therapeutic agent or any compound of one aspect of this invention to said subject at another time during a course of treatment.
  • co-administering as used herein with respect to an additional cancer treatment means that the additional cancer treatment may occur prior to, consecutively with, concurrently with or following the administration of a compound of one aspect of this invention.
  • the additional cancer therapeutic agent is a chemotherapy agent.
  • chemotherapeutic agents used in cancer therapy include, for example,
  • antimetabolites e.g., folic acid, purine, and pyrimidine derivatives
  • alkylating agents e.g., nitrogen mustards, nitrosoureas, platinum, alkyl sulfonates, hydrazines, triazenes, aziridines, spindle poison, cytotoxic agents, topoisomerase inhibitors and others
  • hypomethylating agents e.g. , decitabine (5-aza-deoxycytidine), zebularine, isothiocyanates, azacitidine (5- azacytidine), 5-flouro-2'-deoxycytidine, 5,6-dihydro-5-azacytidine and others.
  • Exemplary agents include Aclarubicin, Actinomycin, Alitretinoin, Altretamine, Aminopterin,
  • Aminolevulinic acid Amrubicin, Amsacrine, Anagrelide, Arsenic trioxide, Asparaginase, Atrasentan, Belotecan, Bexarotene, bendamustine, Bleomycin, Bortezomib, Busulfan,
  • Pirarubicin Pixantrone, Plicamycin, Porfimer sodium, Prednimustine, Procarbazine, Raltitrexed, Ranimustine, Rubitecan, Sapacitabine, Semustine, Sitimagene ceradenovec, Strataplatin, Streptozocin, Talaporfin, Tegafur-uracil, Temoporfin, Temozolomide, Teniposide, Tesetaxel, Testolactone, Tetranitrate, Thiotepa, Tiazofurine, Tioguanine, Tipifarnib, Topotecan,
  • Triaziquone Triethylenemelamine
  • Triplatin Tretinoin, Treosulfan, Trofosfamide, Uramustine, Valrubicin, Verteporfin, Vinblastine, Vincristine, Vindesine, Vinflunine,
  • Vinorelbine Vinorelbine, Vorinostat, Zorubicin, and other cytostatic or cytotoxic agents described herein.
  • two or more drugs are often given at the same time.
  • two or more chemotherapy agents are used as combination chemotherapy.
  • the additional cancer therapeutic agent is a differentiation agent.
  • differentiation agent includes retinoids (such as all-trans-retinoic acid (ATRA), 9-cis retinoic acid, lS-ds-retinoic acid (13-cRA) and 4-hydroxy-phenretinamide (4-HPR)); arsenic trioxide; histone deacetylase inhibitors HDACs (such as azacytidine (Vidaza) and butyrates (e.g., sodium phenylbutyrate)); hybrid polar compounds (such as hexamethylene bisacetamide
  • HMBA hydroxy-3-methyl-4-(HEA)
  • vitamin D hydroxy-3-methyl-4-(HEA)
  • cytokines such as colony-stimulating factors including G-CSF and GM-CSF, and interferons.
  • the additional cancer therapeutic agent is a targeted therapy agent.
  • Targeted therapy constitutes the use of agents specific for the deregulated proteins of cancer cells.
  • Small molecule targeted therapy drugs are generally inhibitors of enzymatic domains on mutated, overexpressed, or otherwise critical proteins within the cancer cell.
  • Prominent examples are the tyrosine kinase inhibitors such as Axitinib, Bosutinib, Cediranib, dasatinib, erlotinib, imatinib, gefitinib, lapatinib, Lestaurtinib, Nilotinib, Semaxanib, Sorafenib, Sunitinib, and Vandetanib, and also cyclin-dependent kinase inhibitors such as Alvocidib and Seliciclib.
  • Monoclonal antibody therapy is another strategy in which the therapeutic agent is an antibody which specifically binds to a protein on the surface of the cancer cells. Examples include the anti-HER2/neu antibody trastuzumab (HERCEPTIN®) typically used in breast cancer, and the anti-CD20 antibody rituximab and Tositumomab typically used in a variety of B-cell
  • exemplary antibodies include Cetuximab, Panitumumab, Trastuzumab, Alemtuzumab, Bevacizumab, Edrecolomab, and Gemtuzumab.
  • exemplary fusion proteins include Aflibercept and Denileukin diftitox.
  • the targeted therapy can be used in combination with a compound described herein, e.g., a biguanide such as metformin or phenformin, preferably phenformin.
  • Targeted therapy can also involve small peptides as "homing devices” which can bind to cell surface receptors or affected extracellular matrix surrounding the tumor. Radionuclides which are attached to these peptides (e.g., RGDs) eventually kill the cancer cell if the nuclide decays in the vicinity of the cell.
  • RGDs Radionuclides which are attached to these peptides
  • An example of such therapy includes BEXXAR®.
  • the additional cancer therapeutic agent is an immunotherapy agent.
  • Cancer immunotherapy refers to a diverse set of therapeutic strategies designed to induce the subject's own immune system to fight the tumor. Contemporary methods for generating an immune response against tumors include intravesicular BCG immunotherapy for superficial bladder cancer, and use of interferons and other cytokines to induce an immune response in renal cell carcinoma and melanoma subjects.
  • Allogeneic hematopoietic stem cell transplantation can be considered a form of immunotherapy, since the donor's immune cells will often attack the tumor in a
  • the immunotherapy agents can be used in combination with a compound or composition described herein.
  • the additional cancer therapeutic agent is a hormonal therapy agent.
  • the growth of some cancers can be inhibited by providing or blocking certain hormones.
  • hormone- sensitive tumors include certain types of breast and prostate cancers. Removing or blocking estrogen or testosterone is often an important additional treatment.
  • administration of hormone agonists, such as progestogens may be therapeutically beneficial.
  • the hormonal therapy agents can be used in combination with a compound or a composition described herein.
  • Other possible additional therapeutic modalities include imatinib, gene therapy, peptide and dendritic cell vaccines, synthetic chlorotoxins, and radiolabeled drugs and antibodies.
  • LAH lithium aluminum hydride
  • HATU NaBH 4 - sodium borohydride
  • LDA lithium diisopropylamide methyluronium
  • reagents were purchased from commercial sources (including Alfa, Acros, Sigma Aldrich, TCI and Shanghai Chemical Reagent Company), and used without further purification.
  • Nuclear magnetic resonance (NMR) spectra were obtained on a Brucker AMX-400 NMR (Brucker, Switzerland). Chemical shifts were reported in parts per million (ppm, ⁇ ) downfield from tetramethylsilane.
  • Mass spectra were run with electrospray ionization (ESI) from a Waters LCT TOF Mass Spectrometer (Waters, USA).
  • a stereoisomer e.g., an (R) or (S) stereoisomer
  • a preparation of that compound such that the compound is enriched at the specified stereocenter by at least about 90%, 95%, 96%, 97%, 98%, or 99%.
  • the chemical name of each of the exemplary compound described below is generated by ChemDraw software.
  • step 1 Preparation of 2,4-dichloro-6-phenyl-l,3,5-triazine (2).
  • phenylmagnesium bromide (217 mL, 0.651 mol, 3 M in ether) dropwise at -10 to -0°C under N 2 protection.
  • the mixture was warmed to room temperature and stirred for 2 hrs.
  • the reaction was cooled to 0°C and quenched by addition of saturated NH 4 C1 (200 mL), then extracted with ethyl acetate.
  • Example 1, step 2 Preparation of 4-chloro-N-isopropyl-6-phenyl-l,3,5-triazin-2-amine (3).
  • a solution of 2,4-dichloro-6-phenyl-l,3,5-triazine (2; 20 g, 0.089 mol) in anhydrous THF (150 mL) was added dropwise a solution of isopropylamine (5.25 g, 0.089 mol) in THF (10 mL) at room temperature via syringe under N 2 . After the addition, the mixture was stirred at room temperature under N 2 for 16 hrs. The reaction was quenched by water (150 mL) and extracted with ethyl acetate. The organic layer was dried, concentrated and purified via Si0 2 chromatography to afford 4-chloro-N-isopropyl-6-phenyl-l,3,5-triazin-2-amine (3) as white solid.
  • N 2 -isopropyl-I ⁇ -(2-methylpyridin-4-yl)-6 ⁇ henyl-l,3,5-triazine-2,4-diamine N 2 -isopropyl-I ⁇ -(2-methylpyridin-4-yl)-6 ⁇ henyl-l,3,5-triazine-2,4-diamine.
  • 4-chloro-6-phenyl-[l,3,5]triazin-2-yl)-isopropyl-amine (3; 150 mg, 0.6 mmol) in DMSO (2 mL) was added 2-methylpyridin-4-amin (78.4 mg, 0.73 mmol), CsF (310 mg, 1.21 mmol) and DIPEA (230 mg, 1.81 mmol).
  • the mixture was stirred at 80°C for 2 h.
  • the mixture was cooled down to rt and filtered to remove the solid.
  • the filtrate was purified by a standard method to give
  • Example 2 Preparation of Compounds of Formula I Wherein Ring A is Optionally Substituted Pyridin-2-yl or Pyrimnidin-2-yl.
  • the compounds of this Example are prepared by general Scheme 2, set forth below.
  • step 1 Preparation of l-phenyl-2-cyanoguanidine (5).
  • a solution of NaN(CN) 2 50 g, 0.5618 mol
  • water 430 mL
  • aniline 26.2 g, 0.28 mol
  • HCI 132 mL/23.5 mL
  • the mixture was heated to 90°C for 16 hours.
  • the mixture was cooled to room temperature and quenched by adding saturated sodium bicarbonate (317 mL).
  • the mixture was filtered and the filter cake was dried via vacuum to afford
  • step 1 was used to produce the following intermediates (5) using the appropriate starting material 4.
  • step 2 Preparation of l-phenyl-2-isopropylamine-diguanidine(7) .
  • l-phenyl-2-cyanoguanidine 5.0 g, 0.031 mol
  • ethanol/water 46mL/18.4 mL
  • CuS0 4 .5H 2 0 3.91 g, 0.01563 mol
  • isopropyl amine 5.53 g, .03975 mol
  • the mixture was heated to reflux for 16 hours.
  • water 137 mL
  • aq.HCl (15.5 mL in 93 mL of water
  • step 2 was used to produce the following intermediates (7) using the appropriate intermediate 5 and the appropriate amine 6.
  • N-isopropyl-N'-phenyl-6-pyridin-2-yl-[l,3,5]triazine-2,4-diamine 0.5 g, 2.28 mmol
  • pyridine-2-carboxylic acid methyl ester 0.312 g, 2.28 mmol
  • NaOMe 0.25 g, 4.56 mmol
  • step 1 Preparation of 6-chloro-pyridine-2-carboxylic acid methyl ester (10).
  • methanol 770 ml
  • concentrated HC1 6 ml
  • the mixture was stirred at 80°C for 48 hours then concentrated to remove the volatile.
  • the crude product was diluted with ethyl acetated and washed with Sat. NaHCC"3 solution.
  • the organic layer was dried with anhydrous Na 2 S04 and concentrated to give -chloro-pyridine-2-carboxylic acid methyl ester as a white solid.
  • LC-MS m/z 172.0 (M+H) + .
  • step 1 was used to produce the following intermediates (10) using the appropriate starting material 9.
  • step 2 Preparation of 6-(6-chloropyridin-2-yl)-l,3,5-triazine-2,4-dione .
  • methyl 6-chloropicolinate 32 g, 0.16 mol
  • biuret 5.3 g, 0.052 mol
  • step 2 was used to produce the following intermediates (11) starting with appropriate intermediate 10.
  • step 3 Preparation of2,4-dichloro-6-(6-chloropyridin-2-yl)-l,3,5-triazine
  • 6-(pyridin-2-yl)-l,3,5-triazine-2,4(lH,3H)-dione (3.0 g, 013 mol) in POCl 3 (48 mL)
  • PC1 5 23 g, 0.1 mol
  • the mixture was stirred at 100°C for 2 hours then concentrated to remove the volatile.
  • the residue was diluted with ethyl acetated and washed with Sat.NaHC0 3 solution.
  • the organic layer was dried over anhydrous Na 2 S0 4 and concentrated to give 2,4-dichloro-6-(6-chloropyridin-2-yl)-l,3,5-triazine as a brown solid.
  • step 4 Preparation of 4-chloro-6-(6-chloropyridin-2-yl)-N-isopropyl-l, 3,
  • step 1 Preparation of 4,6-dichloro-N-isopropyl-l,3,5-triazin-2-amine.
  • THF 25 mL
  • isopropyl amine 1.27 g, 0.0217 mmol
  • the mixture was stirred at room temperature for 12 hours.
  • the mixture was adjusted pH 7 by aq NaHC0 3 and extracted with ethyl acetate (100 mL*2).
  • the combined organic layer was dried over Na 2 S0 4 , concentrated and purified by column
  • step 3 Compound 317 -
  • N-Cyclobutyl-6-(2-fluoro-phenyl)-N'-(5-fluoro-pyridin-3-yl)-[l,3,5]triazine-2,4-di ⁇ A mixture of [4-chloro-6-(2-fluoro-phenyl)-[l,3,5]triazin-2-yl]-cyclobutyl-amine (300 mg, 1.08 mmol), 5-fluoro-pyridin-3-ylamine (145 mg, 1.29 mmol) Pd(dppf)Cl 2 (80 mg, O.l lmmol) and t-BuONa (208 mg, 2.17 mmol) in dioxane (15 mL)was stirred at 80°C under N 2 for 2 hrs.

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Abstract

Provided are compounds useful for treating cancer and methods of treating cancer comprising administering to a subject in need thereof a compound described herein.

Description

THERAPEUTICALLY ACTIVE COMPOUNDS AND THEIR METHODS OF USE
CLAIM OF PRIORITY
This application claims priority from U.S. S.N. 61/584,214, filed January 6, 2012 which is incorporated herein by reference in its entirety.
BACKGROUND OF INVENTION
Isocitrate dehydrogenases (IDHs) catalyze the oxidative decarboxylation of isocitrate to 2-oxoglutarate (i.e., a-ketoglutarate). These enzymes belong to two distinct subclasses, one of which utilizes NAD(+) as the electron acceptor and the other NADP(+). Five isocitrate dehydrogenases have been reported: three NAD(+)-dependent isocitrate dehydrogenases, which localize to the mitochondrial matrix, and two NADP(+)-dependent isocitrate dehydrogenases, one of which is mitochondrial and the other predominantly cytosolic. Each NADP(+)-dependent isozyme is a homodimer.
IDH2 (isocitrate dehydrogenase 2 (NADP+), mitochondrial) is also known as IDH; IDP; IDHM; IDPM; ICD-M; or mNADP-IDH. The protein encoded by this gene is the
NADP(+)-dependent isocitrate dehydrogenase found in the mitochondria. It plays a role in intermediary metabolism and energy production. This protein may tightly associate or interact with the pyruvate dehydrogenase complex. Human IDH2 gene encodes a protein of 452 amino acids. The nucleotide and amino acid sequences for IDH2 can be found as GenBank entries NM_002168.2 and NP_002159.2 respectively. The nucleotide and amino acid sequence for human IDH2 are also described in, e.g., Huh et al., Submitted (NOV-1992) to the
EMBL/GenBank/DDBJ databases; and The MGC Project Team, Genome Res.
14:2121-2127(2004).
Non-mutant, e.g., wild type, IDH2 catalyzes the oxidative decarboxylation of isocitrate to a-ketoglutarate (a- KG) thereby reducing NAD+ (NADP+) to NADH (NADPH), e.g., in the forward reaction:
Isocitrate + NAD+ (NADP+)→ a-KG + C02 + NADH (NADPH) + H+.
It has been discovered that mutations of IDH2 present in certain cancer cells result in a new ability of the enzyme to catalyze the NAPH-dependent reduction of α-ketoglutarate to R(-)-2-hydroxyglutarate (2HG). 2HG is not formed by wild- type IDH2. The production of 2HG is believed to contribute to the formation and progression of cancer (Dang, L et al, Nature 2009, 462:739-44).
The inhibition of mutant IDH2 and its neoactivity is therefore a potential therapeutic treatment for cancer. Accordingly, there is an ongoing need for inhibitors of IDH2 mutants having alpha hydroxyl neoactivity.
SUMMARY OF INVENTION
Described herein are compounds of Structural Formula I, or a pharmaceutically acceptable salt or hydrate thereof:
Figure imgf000003_0001
wherein:
ring A is an optionally substituted 5-6 member monocyclic aryl or monocyclic heteroaryl;
ring B is an optionally substituted 5-6 member monocyclic aryl or monocyclic heteroaryl;
1 3
R and RJ are each independently selected from hydrogen, C C4 alkyl, C C4 haloalkyl, -0-Ci-C4 alkyl, and CN, wherein any alkyl portion of R1 is optionally substituted with -OH, NH2, NH(Ci-C4 alkyl), or N(C C4 alkyl)2;
R is selected from: -(C -C alkyl), -(C2-C6 alkenyl or alkynyl), -(C -C
alkylene)-N(R6)-(Ci-C6 alkylene)-0-(Ci-C6 alkyl), -(Ci-C6 alkylene)-N(R6)-(C0-C6 alkylene)-Q, -(Ci-C6 alkylene)-N(R6)(R6), -(Ci-Ce alkylene)-N(R6)-S(0)1_2-(C1-C6 alkyl), -(Ci-Ce alkylene)-N(R6)-S(0)i_2-(Co-C6 alkyl)-Q, -(Ci-C6 alkylene)-S(0)i-2-N(R6)(R6), -(Ci-C4 alkylene)-S(0)i_2-N(R6)-(Ci-C6 alkylene)-Q, -C(0)N(R6)-(d-C6 alkylene)-C(O)- (Co-C6 alkylene)-0-(Ci-C6 alkyl), -C(0)N(R6)-(Ci-C6 alkylene)-C(O)-(C0-C6
alkylene)-O-(C0-C6 alkylene)-Q, -(Ci-Ce alkylene)-0-C(0)-(C1-C6 alkyl), -(Ci-Ce alkylene)-O-C(O)-(C0-C6 alkyl)-Q, -(Ci-C6 alkylene)-0-(C1-C6 alkyl), -(Ci-C6 alkylene)-0-(C1-C6 alkylene)-Q, -(C0-C6 alkylene)-C(O)-(C0-C6 alkylene)-0-(C1-C6 alkyl), -(Co-C6 alkylene)-C(O)-(C0-C6 alkylene)-0-(Ci-C6 alkylene)-Q, -(Ci-C6 alkylene)-0-C(0)-(Ci-C6 alkyl), -(Ci-C6 alkylene)-O-C(O)-(C0-C6 alkylene)-Q, -(C0-C6 alkylene)-C(0)N(R6)-(Ci-C6 alkyl), -(C0-C6 alkylene)-C(O)N(R6)-(C0-C6 alkylene)-Q, -(Ci-Ce alkylene)-N(R6)C(0)-(C1-C6 alkyl), -(Ci-C6 alkylene)-N(R6)C(O)-(C0-C6 alkylene)-Q, -(C0-C6 alkylene)-S(0)o-2-(Ci-C6 alkyl), -(C0-C6 alkylene)-S(0)0-2-(Co-C6 alkylene)-Q, -(Ci-C6 alkylene)-N(R6)-C(0)-N(R6)-(Ci-C6 alkyl), -(C0-C6 alkylene)-Q, -(Co-Ce alkylene)-C(0)-(Ci-C6 alkyl), -(C0-C6 alkylene)-C(O)-(C0-C6 alkylene)-Q, wherein:
any alkyl or alkylene moiety present in R is optionally substituted with one or more -OH, -0(Ci-C4 alkyl) or halo;
any terminal methyl moiety present in R is optionally replaced with -CH2OH,
CF3, -CH2F, -CH2CI, C(0)CH3, C(0)CF3, CN, or C02H;
each R6 is independently selected from hydrogen and CrC6 alkyl; and
Q is selected from aryl, heteroaryl, carbocyclyl and heterocyclyl, any of which is optionally substituted; or
R 1 and R 3J are optionally taken together with the carbon to which they are attached to form C(=0); or
R 1 and R 2" are optionally taken together to form substituted carbocyclyl, optionally substituted heterocyclyl or optionally substituted heteroaryl, wherein:
a. when ring A is unsubstituted phenyl, and ring B is phenyl substituted by methoxy or ethoxy; then said phenyl of ring B is not further substituted by oxazolyl;
b. when ring A is optionally substituted phenyl or optionally substituted pyridyl, and ring B is optionally substituted phenyl; then the portion of the compound represented by -NH-C^XR2)^3) is not -NH(CH2)-aryl;
c. when ring A is optionally substituted phenyl, and ring B is optionally substituted phenyl or pyrrolyl; then the portion of the compound represented by
-NH-C^XR2)^3) is not -NH(CH2)C(0)NH2; d. when ring A is phenyl substituted with 2 or more hydroxyl or methoxy, and ring B is optionally substituted phenyl; then the portion of the compound represented by -NH-C^XR2)^3) is not -NH-cycloheptyl;
e. when ring A is optionally substituted phenyl and ring B is optionally substituted phenyl; then R 1 and R 3 do not form 2,2,6, 6,-tetramethylpiperidin-4-yl;
f. when ring A and ring B are optionally substituted phenyl; then the portion of the compound represented by -NH-C(R 1 )(R2 )(R 3 ) is not cysteine, optionally substituted phenylalanine or leucine or methyl ester thereof;
g. when ring A is phenyl or pyridin-3-yl optionally substituted with one or more substituents selected from halo, methyl or CF3, and ring B is phenyl optionally substituted with one or more substituents selected from halo, methyl, CF3, methoxy, CH=C(phenyl)CN; then the portion of the compound represented by -NFK R^R2)^3) is other than -NH(Ci-C8 alkylene)-N(Ra)(Ra),
-NH-l-(aminomethyl)cyclopentylmethyl,
-NH-4-(aminomethyl)cyclohexylmethyl, wherein each Ra is hydrogen, CrC4 alkyl or two Ras are taken together with the nitrogen to which they are commonly bound to form morpholin-4-yl or pipieridin-l-yl;
h. when ring A is phenyl, 4-chlorophenyl or 4-methyl phenyl and ring B is
4-chlorophenyl or 3,4-dichlorophenyl; then the portion of the compound represented by -NHC(R1)(R2)(R3) is not -NH-isopropyl;
i. when ring A is unsubstituted phenyl and the portion of the compound represented by -NHC(R1)(R2)(R3) is -NH-CH2CH2N(CH3)2, -NH-CH2CH2-morpholin-4-yl or -NH-CH2CH2OH; then ring B is other than oxadiazole, imidazole, thiazole or oxazole each of which is substituted with -C(0)NHRb, wherein Rb is isopropyl, cyclopropyl or 2-chloro-6-methylphenyl;
j. when ring A is phenyl substituted with S02OH or S02Na and ring B is phenyl, or when ring B is phenyl substituted with S02OH and ring A is substituted phenyl; then the portion of the compound represented by -NHC(R 1 )(R2 )(R 3 ) is not -NH(CH2)2OH or -NH(CH2)CH(OH)CH3; and
k. the compound is other than: (E)-3-(4-((4-((3-(diethylamino)propyl)amino)-6-phenyl-l,3,5-triazin-2-yl)amino)-2- methoxyphenyl)-2-phenylacrylonitrile ,
4-((4-((furan-2-ylmethyl)amino)-6-(pyridin-4-yl)- l,3,5-triazin-2-yl)amino)phenol, 3- (4- ((5-aminopentyl)amino)-6-((3-fluorophenyl)amino)-l,3,5-triazin-2-yl)phenol,
2 4
N ,6-bis(3-fluorophenyl)-N -(piperidin-3-yl)- l,3,5-triazine-2,4-diamine,
2 4 2 4
N -butyl-6-phenyl-N -(p-tolyl)-l,3,5-triazine-2,4-diamine, N -cyclohexyl-N ,6-diphenyl- l,3,5-triazine-2,4-diamine,
(R)-3-((4-(3-chlorophenyl)-6-(pyrrolidin-3-ylamino)-l,3,5-triazin-2-yl)arnino)-4- methylbenzamide,
2-chloro-4-(methylsulfonyl)-N-[4-(phenylamino)-6-(2-pyridinyl)-l,3,5-triazin-2-yl]- benzamide,
N2^2-methoxyethyl)-A^-phenyl-6-[5-[6-(2,2,2-trifluoroethoxy)-3-pyridinyl]- l,2,4- oxadiazol-3-yl]-l,3,5-triazine-2,4-diamine,
2 4
N -(2-furanylmethyl)-6-phenyl-N -[3-(trifluoromethyl)phenyl]-l,3,5-triazine-2,4- diamine,
6-(3-methoxyphenyl)-N2-methyl-A^-(3-nitrophenyl)- l,3,5-triazine-2,4-diamine,
N2-butyl-N4-(4-methylphenyl)-6-phenyl- 1 ,3,5-triazine-2,4-diamine, and
4-[[4-(5-chloro-2-methylphenyl)-6-(methylamino)]-l,3,5-triazin-2-yl]amino- benzenemethanol .
The compound of Formula I or II or as decribed in any one of the embodiments herein inhibits mutant IDH2, particularly mutant IDH2 having alpha hydroxyl neoactivity. Also described herein are pharmaceutical compositions comprising a compound of Formula I and methods of using such compositions to treat cancers characterized by the presence of a mutant IDH2.
DETAILED DESCRIPTION
The details of construction and the arrangement of components set forth in the following description or illustrated in the drawings are not meant to be limiting. Other embodiments and different ways to practice the invention are expressly included. Also, the phraseology and terminology used herein is for the purpose of description and should not be regarded as limiting. The use of "including," "comprising," or "having," "containing", "involving", and variations thereof herein, is meant to encompass the items listed thereafter and equivalents thereof as well as additional items.
Definitions:
The term "halo" or "halogen" refers to any radical of fluorine, chlorine, bromine or iodine.
The term "alkyl" refers to a fully saturated or unsaturated hydrocarbon chain that may be a straight chain or branched chain, containing the indicated number of carbon atoms. For example, CrC12 alkyl indicates that the group may have from 1 to 12 (inclusive) carbon atoms in it. The term "haloalkyl" refers to an alkyl in which one or more hydrogen atoms are replaced by halo, and includes alkyl moieties in which all hydrogens have been replaced by halo (e.g., perfluoroalkyl). The terms "arylalkyl" or "aralkyl" refer to an alkyl moiety in which an alkyl hydrogen atom is replaced by an aryl group. Aralkyl includes groups in which more than one hydrogen atom has been replaced by an aryl group. Examples of "arylalkyl" or "aralkyl" include benzyl, 2-phenylethyl, 3-phenylpropyl, 9-fluorenyl, benzhydryl, and trityl groups. The term "alkyl" includes "alkenyl" and "alkynyl".
The term "alkylene" refers to a divalent alkyl, e.g., -CH2-, -CH2CH2-, -CH2CH2CH2- and -CH2CH(CH3)CH2-.
The term "alkenyl" refers to a straight or branched hydrocarbon chain containing 2-12 carbon atoms and having one or more double bonds. Examples of alkenyl groups include, but are not limited to, allyl, propenyl, 2-butenyl, 3-hexenyl and 3-octenyl groups. One of the double bond carbons may optionally be the point of attachment of the alkenyl substituent.
The term "alkynyl" refers to a straight or branched hydrocarbon chain containing 2-12 carbon atoms and characterized in having one or more triple bonds. Examples of alkynyl groups include, but are not limited to, ethynyl, propargyl, and 3-hexynyl. One of the triple bond carbons may optionally be the point of attachment of the alkynyl substituent.
The term "alkoxy" refers to an -O-alkyl radical. The term "haloalkoxy" refers to an alkoxy in which one or more hydrogen atoms are replaced by halo, and includes alkoxy moieties in which all hydrogens have been replaced by halo (e.g., perfluoroalkoxy). Unless otherwise specified, the term "aryl" refers to a fully aromatic monocyclic, bicyclic, or tricyclic hydrocarbon ring system. Examples of aryl moieties are phenyl, naphthyl, and anthracenyl. Unless otherwise specified, any ring atom in an aryl can be substituted by one or more substituents. The term "monocyclic aryl" means a monocyclic fully romatic
hydrocarbon ring system, optionally substituted by one or more substituents which can not form a fused bicyclic or tricyclic ring.
The term "carbocyclyl" refers to a non-aromatic, monocyclic, bicyclic, or tricyclic hydrocarbon ring system. Carbocyclyl groups include fully saturated ring systems (e.g., cycloalkyls), and partially saturated ring systems.
The term "cycloalkyl" as employed herein includes saturated cyclic, bicyclic, tricyclic, or polycyclic hydrocarbon groups having 3 to 12 carbons. Any ring atom can be substituted (e.g., by one or more substituents). Examples of cycloalkyl moieties include, but are not limited to, cyclopropyl, cyclohexyl, methylcyclohexyl, adamantyl, and norbornyl.
Unless otherwise specified, the term "heteroaryl" refers to a fully aromatic 5-8 membered monocyclic, 8-12 membered bicyclic, or 11-14 membered tricyclic ring system having 1-3 heteroatoms if monocyclic, 1-6 heteroatoms if bicyclic, or 1-9 heteroatoms if tricyclic, said heteroatoms selected from O, N, or S (or the oxidized forms such as N+-0", S(O) and S(0)2). The term "monocyclic heteroaryl" means a monocyclic fully romatic ring system having 1-3 heteroatoms, optionally substituted by one or more substituents which can not form a fused bicyclic or tricyclic ring.
The term "heterocyclyl" refers to a nonaromatic, 3-10 membered monocyclic, 8-12 membered bicyclic, or 11-14 membered tricyclic ring system having 1-3 heteroatoms if monocyclic, 1-6 heteroatoms if bicyclic, or 1-9 heteroatoms if tricyclic, said heteroatoms selected from O, N, or S (or the oxidized forms such as N+-0", S(O) and S(0)2). The heteroatom may optionally be the point of attachment of the heterocyclyl substituent. Examples of heterocyclyl include, but are not limited to, tetrahydrofuranyl, tetrahydropyranyl, piperidinyl, morpholino, pyrrolinyl, pyrimidinyl, and pyrrolidinyl. Heterocyclyl groups include fully saturated ring systems, and partially saturated ring systems.
Bicyclic and tricyclic ring systems containing one or more heteroatoms and both aromatic and non-aromatic rings are considered to be heterocyclyl or heteroaryl groups. Bicyclic or tricyclic ring systems where an aryl or a heteroaryl is fused to a carbocyclyl or heterocyclyl and the point of attachment from the ring system to the rest of the molecule is through an aromatic ring are considered to be aryl or heteroaryl groups, respectively Bicyclic or tricyclic ring systems where an aryl or a heteroaryl is fused to a carbocyclyl or heterocyclyl and the point of attachment from the ring system to the rest of the molecule is through the non-aromatic ring are considered to be carbocyclyl (e.g., cycloalkyl) or heterocyclyl groups, respectively.
Aryl, heteroaryl, carbocyclyl (including cycloalkyl), and heterocyclyl groups, either alone or a part of a group (e.g., the aryl portion of an aralkyl group), are optionally substituted at one or more substitutable atoms with, unless specified otherwise, substituents independently selected from: halo, -C≡N, C1-C4 alkyl, =0, -ORb, -ORb', -SRb, -SRb', -(C1-C4 alkyl)-N(Rb)(Rb), -(C1-C4 alkyl)-N(Rb)(Rb'), -N(Rb)(Rb), -N(Rb)(Rb ), -0-(Ci-C4 alkyl)-N(Rb)(Rb), -0-(CrC4
alkyl)-N(Rb)(Rb'), -(d-C4 alkyl)-0-(Ci-C4 alkyl)-N(Rb)(Rb), -(d-C4 alkyl)-0-(Ci-C4
alkyl)-N(Rb)(Rb'), -C(0)-N(Rb)(Rb), -(d-C4 alkyl) -C(0)-N(Rb)(Rb), -(C C4
alkyl)-C(0)-N(Rb)(Rb'), -ORb', Rb', -C(0)(Ci-C4 alkyl), -C(0)Rb', -C(0)N(Rb')(Rb),
-N(Rb)C(0)(Rb), -N(Rb)C(0)(Rb'), -N(Rb)S02(Rb), -S02N(Rb)(Rb), -N(Rb)S02(Rb'), and
-S02N(Rb)(Rb ), wherein any alkyl substituent is optionally further substituted with one or more of -OH, -0-(Ci-C4 alkyl), halo, -NH2, -NH(Ci-C4 alkyl), or -N(C C4 alkyl)2;
each Rb is independently selected from hydrogen, and -Q-C4 alkyl; or two Rbs are taken together with the nitrogen atom to which they are bound to form a 4- to 8-membered heterocyclyl optionally comprising one additional heteroatom selected from N, S, and O; and
each Rb is independently selected from C3-C7 carbocyclyl, phenyl, heteroaryl, and heterocyclyl, wherein one or more substitutable positions on said phenyl, cycloalkyl, heteroaryl or heterocycle substituent is optionally further substituted with one or more of -(Q-C4 alkyl), -(C C4 fluoroalkyl), -OH, -0-(C C4 alkyl), -0-(C C4 fluoroalkyl), halo, -NH2,
-NH(CrC4 alkyl), or -N(C C4 alkyl)2.
Heterocyclyl groups, either alone or as part of a group, are optionally substituted on one or more any substitutable nitrogen atom with oxo, -Q-C4 alkyl, or fluoro-substituted Q-C4 alkyl.
The term "substituted" refers to the replacement of a hydrogen atom by another group. As used herein, the term "elevated levels of 2HG" means 10%, 20% 30%, 50%, 75%, 100%, 200%, 500% or more 2HG then is present in a subject that does not carry a mutant IDH2 allele. The term "elevated levels of 2HG" may refer to the amount of 2HG within a cell, within a tumor, within an organ comprising a tumor, or within a bodily fluid.
The term "bodily fluid" includes one or more of amniotic fluid surrounding a fetus, aqueous humour, blood (e.g., blood plasma), serum, Cerebrospinal fluid, cerumen, chyme, Cowper's fluid, female ejaculate, interstitial fluid, lymph, breast milk, mucus (e.g., nasal drainage or phlegm), pleural fluid, pus, saliva, sebum, semen, serum, sweat, tears, urine, vaginal secretion, or vomit.
As used herein, the terms "inhibit" or "prevent" include both complete and partial inhibition and prevention. An inhibitor may completely or partially inhibit the intended target.
The term "treat" means decrease, suppress, attenuate, diminish, arrest, or stabilize the development or progression of a disease/disorder (e.g., a cancer), lessen the severity of the disease/disorder (e.g., a cancer) or improve the symptoms associated with the disease/disorder (e.g., a cancer).
As used herein, an amount of a compound effective to treat a disorder, or a
"therapeutically effective amount" refers to an amount of the compound which is effective, upon single or multiple dose administration to a subject, in treating a cell, or in curing, alleviating, relieving or improving a subject with a disorder beyond that expected in the absence of such treatment.
As used herein, the term "subject" is intended to include human and non-human animals. Exemplary human subjects include a human patient (referred to as a patient) having a disorder, e.g., a disorder described herein or a normal subject. The term "non-human animals" of one aspect of the invention includes all vertebrates, e.g., non-mammals (such as chickens, amphibians, reptiles) and mammals, such as non-human primates, domesticated and/or agriculturally useful animals, e.g., sheep, dog, cat, cow, pig, etc.
Compounds Provided is a compound of Structural Formula I, or a pharmaceutically acceptable salt or hydrate thereof:
Figure imgf000011_0001
wherein:
ring A is an optionally substituted 5-6 member monocyclic aryl or monocyclic heteroaryl; ring B is an optionally substituted 5-6 member monocyclic aryl or monocyclic heteroaryl;
R 1 and R 3J are each independently selected from hydrogen, CrC4 alkyl, CrC4 haloalkyl, -0-Ci-C4 alkyl, and CN, wherein any alkyl portion of R1 is optionally substituted with -OH, NH2, NH(Ci-C4 alkyl), or N(Ci-C4 alkyl)2;
R is selected from: -(CrC6 alkyl), -(C2-C6 alkenyl or alkynyl), -(CrC6
alkylene)-N(R6)-(C1-C6 alkylene)-0-(C1-C6 alkyl), -(Ci-C6 alkylene)-N(R6)-(C0-C6 alkylene)-Q, -(Ci-Ce alkylene)-N(R6)(R6), -(Ci-C6 alkylene)-N(R6)-S(0)i_2-(Ci-C6 alkyl), -(Ci-C6
alkylene)-N(R6)-S(0)i_2-(Co-C6 alkyl)-Q, -(Ci-C6 alkylene)-S(0)i_2-N(R6)(R6), -(Ci-C4 alkylene)-S(0)1-2-N(R6)-(C1-C6 alkylene)-Q, -C(0)N(R6)-(Ci-C6 alkylene)-C(O)- (C0-C6 alkylene)-0-(C1-C6 alkyl), -C(0)N(R6)-(Ci-C6 alkylene)-C(O)-(C0-C6 alkylene)-O-(C0-C6 alkylene)-Q, -(Ci-C6 alkylene)-0-C(0)-(Ci-C6 alkyl), -(Ci-C6 alkylene)-O-C(O)-(C0-C6 alkyl)-Q, -(Ci-Ce alkylene)-0-(Ci-C6 alkyl), -(Ci-C6 alkylene)-0-(Ci-C6 alkylene)-Q, -(C0-C6
alkylene)-C(O)-(C0-C6 alkylene)-0-(C1-C6 alkyl), -(C0-C6 alkylene)-C(O)-(C0-C6
alkylene)-0-(C1-C6 alkylene)-Q, -(Ci-C6 alkylene)-0-C(0)-(C1-C6 alkyl), -(Ci-C6
alkylene)-O-C(O)-(C0-C6 alkylene)-Q, -(C0-C6 alkylene)-C(0)N(R6)-(Ci-C6 alkyl), -(C0-C6 alkylene)-C(O)N(R6)-(C0-C6 alkylene)-Q, -(Ci-C6 alkylene)-N(R6)C(0)-(Ci-C6 alkyl), -(Ci-C6 alkylene)-N(R6)C(O)-(C0-C6 alkylene)-Q, -(C0-C6 alkylene)-S(O)0-2-(Ci-C6 alkyl), -(C0-C6 alkylene)-S(0)0-2-(Co-C6 alkylene)-Q, -(Ci-C6 alkylene)-N(R6)-C(0)-N(R6)-(C1-C6 alkyl), -(C0-C6 alkylene)-Q, -(C0-C6 alkylene)-C(0)-(Ci-C6 alkyl), -(C0-C6 alkylene)-C(O)-(C0-C6 alkylene)-Q, wherein: any alkyl or alkylene moiety present in R is optionally substituted with one or more -OH, -0(Ci-C4 alkyl) or halo;
any terminal methyl moiety present in R is optionally replaced with -CH2OH, CF3,
-CH2F, -CH2C1, C(0)CH3, C(0)CF3, CN, or C02H;
each R6 is independently selected from hydrogen and C]_-C alkyl; and
Q is selected from aryl, heteroaryl, carbocyclyl and heterocyclyl; and Q is optionally substituted; or
1 3
R and RJ are optionally taken together with the carbon to which they are attached to form C(=0); or
1 2
R and R" are optionally taken together to form an optionally substituted carbocyclyl, optionally substituted heterocyclyl or optionally substituted heteroaryl; wherein:
a. when ring A is unsubstituted phenyl, and ring B is phenyl substituted by methoxy or ethoxy; then said phenyl of ring B is not further substituted by oxazolyl;
b. when ring A is optionally substituted phenyl or optionally substituted pyridyl, and ring B is optionally substituted phenyl; then the portion of the compound represented by -NH-C^XR^R3) is not -NH(CH2)-aryl;
c. when ring A is optionally substituted phenyl, and ring B is optionally substituted phenyl or pyrrolyl; then the portion of the compound represented by -NH-C^XR2)^3) is not -NH(CH2)C(0)NH2;
d. when ring A is phenyl substituted with 2 or more hydroxyl or methoxy, and ring B is optionally substituted phenyl; then the portion of the compound represented by -NH-C(R1)(R2)(R3) is not -NH-cycloheptyl;
e. when ring A is optionally substituted phenyl and ring B is optionally substituted
1 3
phenyl; then R and R do not form 2,2,6, 6,-tetramethylpiperidin-4-yl;
f. when ring A and ring B are optionally substituted phenyl; then the portion of the
1 2 3
compound represented by -NH-C(R )(R )(R ) is not cysteine, optionally substituted phenylalanine or leucine or methyl ester thereof;
g. when ring A is phenyl or pyridin-3-yl optionally substituted with one or more substituents selected from halo, methyl or CF3, and ring B is phenyl optionally substituted with one or more substituents selected from halo, methyl, CF3, methoxy, CH=C(phenyl)CN; then the portion of the compound represented by -NHC^XR2)^3) is other than -NH(Ci-C8 alkylene)-N(Ra)(Ra), -NH-l-(aminomethyl)cyclopentylmethyl,
-NH-4-(aminomethyl)cyclohexylmethyl, wherein each Ra is hydrogen, C C4 alkyl or two Ras are taken together with the nitrogen to which they are commonly bound to form morpholin-4-yl or pipieridin-l-yl;
h. when ring A is phenyl, 4-chlorophenyl or 4-methyl phenyl and ring B is 4-chlorophenyl or 3,4-dichlorophenyl; then the portion of the compound represented by -NHC(R1)(R2)(R3) is not -NH-isopropyl;
i. when ring A is unsubstituted phenyl and the portion of the compound represented by -NHC^XR2)^3) is -NH-CH2CH2N(CH3)2, -NH-CH2CH2-morpholin-4-yl or -NH-CH2CH2OH; then ring B is other than oxadiazole, imidazole, thiazole or oxazole each of which is substituted with -C(0)NHRb, wherein Rb is isopropyl, cyclopropyl or 2-chloro-6-methylphenyl;
j. when ring A is phenyl substituted with S02OH or S02Na and ring B is phenyl, or when ring B is phenyl substituted with S02OH and ring A is substitituted phenyl; then the portion of the compound represented by -NHC(R 1 )(R2 )(R 3 ) is not -NH(CH2)2OH or -NH(CH2)CH(OH)CH3; and
k. the compound is other than:
(E)-3-(4-((4-((3-(diethylamino)propyl)amino)-6-phenyl-l,3,5-triazin-2-yl)amino)-2- methoxyphenyl)-2-phenylacrylonitrile ,
4-((4-((furan-2-ylmethyl)amino)-6-(pyridin-4-yl)-l,3,5-triazin-2-yl)amino)phenol, 3-(4-((5-aminopentyl)amino)-6-((3-fluorophenyl)amino)-l,3,5-triazin-2-yl)phenol,
N 2 ,6-bis(3-fluorophenyl)-N 4 -(piperidin-3-yl)-l,3,5-triazine-2,4-diamine,
N 2 -butyl-6-phenyl-N 4 -(p-tolyl)-l,3,5-triazine-2,4-diamine, N 2 -cyclohexyl-N 4 ,6-diphenyl- l,3,5-triazine-2,4-diamine,
(R)-3-((4-(3-chlorophenyl)-6-(pyrrolidin-3-ylamino)-l,3,5-triazin-2-yl)amino)-4- methylbenzamide, 2-chloro-4-(methylsulfonyl)-N-[4-(phenylamino)-6-(2-pyridinyl)-l,3,5-triazin-2-yl]- benzamide,
N2^2-methoxyethyl)-A^-phenyl-6-[5-[6-(2,2,2-trifluoroethoxy)-3-pyridinyl]- l,2,4- oxadiazol-3-yl]-l,3,5-triazine-2,4-diamine,
2 4
N -(2-furanylmethyl)-6-phenyl-N -[3-(trifluoromethyl)phenyl]-l,3,5-triazine-2,4- diamine,
6-(3-methoxyphenyl)-N2-methyl-A^-(3-nitrophenyl)- l,3,5-triazine-2,4-diamine,
N2-butyl-N4-(4-methylphenyl)-6-phenyl- 1 ,3,5-triazine-2,4-diamine, and
4-[[4-(5-chloro-2-methylphenyl)-6-(methylamino)]-l,3,5-triazin-2-yl]amino- benzenemethanol .
Also provided is a compound of Structural Formula I, or a pharmaceutically acceptable salt or hydrate thereof:
Figure imgf000014_0001
wherein:
ring A is an optionally substituted 5-6 member monocyclic aryl or monocyclic heteroaryl; ring B is an optionally substituted 5-6 member monocyclic aryl or monocyclic heteroaryl;
1 3
R and RJ are each independently selected from hydrogen, CrC4 alkyl, CrC4 haloalkyl, -0-CrC4 alkyl, and CN, wherein any alkyl portion of R1 is optionally substituted with -OH, NH2, NH(Ci-C4 alkyl), or N(C C4 alkyl)2;
R is selected from: -(C -C alkyl), -(C2-C6 alkenyl or alkynyl), -(C -C alkylene)-N(R6)-(C1-C6 alkylene)-0-(C1-C6 alkyl), -(Ci-C6 alkylene)-N(R6)-(C0-C6 alkylene)-Q, -(Ci-C6 alkylene)-N(R6)(R6), -(Ci-Ce alkylene)-N(R6)-S(0)1_2-(C1-C6 alkyl), -(d-C6 alkylene)-N(R6)-S(O)1_2-(C0-C6 alkyl)-Q, -(d-C6 alkylene)-S(0)1_2-N(R6)(R6), -(Ci-C4 alkylene)-S(0)i_2-N(R6)-(Ci-C6 alkylene)-Q, -C(0)N(R6)-(d-C6 alkylene)-C(O)- (Co-C6 alkylene)-0-(C1-C6 alkyl), -C(0)N(R6)-(Ci-C6 alkylene)-C(O)-(C0-C6 alkylene)-O-(C0-C6 alkylene)-Q, -(Ci-C6 alkylene)-0-C(0)-(C1-C6 alkyl), -(Ci-C6 alkylene)-O-C(O)-(C0-C6 alkyl)-Q, -(Ci-C6 alkylene)-0-(C1-C6 alkyl), -(Ci-C6 alkylene)-0-(Ci-C6 alkylene)-Q, -(C0-C6 alkylene)-C(O)-(C0-C6 alkylene)-0-(Ci-C6 alkyl), -(Co-C6 alkylene)-C(O)-(C0-C6 alkylene)-0-(Ci-C6 alkylene)-Q, -(Ci-C6 alkylene)-0-C(0)-(Ci-C6 alkyl), -(Ci-C6 alkylene)-O-C(O)-(C0-C6 alkylene)-Q, -(C0-C6 alkylene)-C(0)N(R6)-(C1-C6 alkyl), -(C0-C6 alkylene)-C(O)N(R6)-(C0-C6 alkylene)-Q, -(Ci-Ce alkylene)-N(R6)C(0)-(C1-C6 alkyl), -(Ci-C6 alkylene)-N(R6)C(O)-(C0-C6 alkylene)-Q, -(C0-C6 alkylene)-S(0)o-2-(Ci-C6 alkyl), -(C0-C6 alkylene)-S(0)0-2-(Co-C6 alkylene)-Q, -(Ci-C6 alkylene)-N(R6)-C(0)-N(R6)-(Ci-C6 alkyl), -(C0-C6 alkylene)-Q, -(Co-Ce alkylene)-C(0)-(C1-C6 alkyl), -(C0-C6 alkylene)-C(O)-(C0-C6 alkylene)-Q, wherein:
any alkyl or alkylene moiety present in R is optionally substituted with one or more -OH, -0(Ci-C4 alkyl) or halo;
any terminal methyl moiety present in R is optionally replaced with -CH2OH,
CF3, -CH2F, -CH2CI, C(0)CH3, C(0)CF3, CN, or C02H;
each R6 is independently selected from hydrogen and C]_-C alkyl; and
Q is selected from aryl, heteroaryl, carbocyclyl and heterocyclyl, any of which is optionally substituted; or
1 3
R and RJ are optionally taken together with the carbon to which they are attached to form C(=0), or
1 2
R and R" are optionally taken together to form substituted carbocyclyl or optionally substituted heterocyclyl, wherein:
a. when ring A is unsubstituted phenyl, and ring B is phenyl substituted by methoxy or ethoxy; then said phenyl of ring B is not further substituted oxazolyl;
b. when ring A is optionally substituted phenyl or optionally substituted pyridyl;
1 2 3
then the portion of the compound represented by -NH-C(R )(R )(R ) is not -NH(CH2)-aryl;
c. when ring A is optionally substituted phenyl, and ring B is optionally substituted phenyl or pyrrolyl; then the portion of the compound represented by
-NH-C^XR2)^3) is not -NH(CH2)C(0)NH2; d. when ring A is phenyl substituted with 2 or more hydroxyl or methoxy, and ring B is optionally substituted phenyl; then the portion of the compound represented by -NH-C^XR2)^3) is not -NH-cycloheptyl;
e. when ring A is optionally substituted phenyl and ring B is optionally substituted phenyl; then R 1 and R 3 do not form 2,2,6, 6,-tetramethylpiperidin-4-yl;
f. when ring A and ring B are optionally substituted phenyl; then the portion of the compound represented by -NH-C(R 1 )(R2 )(R 3 ) is not cysteine, optionally substituted phenylalanine or leucine;
g. when ring A is phenyl or pyridin-3-yl optionally substituted with one or more substituents selected from halo, methyl or CF3, and ring B is phenyl optionally substituted with one or more substituents selected from halo, methyl or CF3; then the portion of the compound represented by -NHC(R 1 )(R2 )(R 3 ) is other than -NH(Ci-C8 alkylene)-N(Ra)(Ra), -NH-l-(aminomethyl)cyclopentylmethyl, -NH-4-(aminomethyl)cyclohexylmethyl, wherein each Ra is hydrogen, CrC3 alkyl or two Ras are taken together with the nitrogen to which they are commonly bound to form morpholin-4-yl or pipieridin-l-yl;
h. when ring A is phenyl, 4-chlorophenyl or 4-methyl phenyl and ring B is 4-chlorophenyl or 3,4-dichlorophenyl; then the portion of the compound represented by -NHC(R1)(R2)(R3) is not -NH-isopropyl;
i. when ring A is unsubstituted phenyl and the portion of the compound represented by -NHC(R1)(R2)(R3) is -NH-CH2CH2N(CH3)2, -NH-CH2CH2-morpholin-4-yl or -NH-CH2CH2OH; then ring B is other than oxadiazole, thiazole or oxazole each of which is substituted with -C(0)NHRb, wherein Rb is isopropyl, cyclopropyl or 2-chloro-6-methylphenyl;
j. when ring A is phenyl substituted with S02OH or S02Na, and ring B is phenyl; then the portion of the compound represented by -NHC(R 1 )(R2 )(R 3 ) is not -NH(CH2)2OH or -NH(CH2)CH(OH)CH3; and
k. the compound is other than:
(E)-3-(4-((4-((3-(diethylamino)propyl)amino)-6-phenyl-l,3,5-triazin-2-yl)amino)-2- methoxyphenyl)-2-phenylacrylonitrile, 4-((4-((furan-2-ylmethyl)amino)-6-(pyridin-4-yl)- 1 ,3,5- triazin-2-yl)amino)phenol, 3-(4-((5-aminopentyl)amino)-6-((3-fluorophenyl)amino)- 1,3,5- triazin-2-yl)phenol, 2 s(3-fluorophenyl 4 2
N ,6-bi )-N -(piperidin-3-yl)-l,3,5-triazine-2,4-diamine, N - butyl-6-phenyl-N4-(p-tolyl)-l,3,5-triazine-2,4-diamine, N2-cyclohexyl-N4,6-diphenyl- 1,3,5- triazine-2,4-diamine, and(R)-3-((4-(3-chlorophenyl)-6-(pyrrolidin-3-ylamino)-l,3,5-triazin-2- yl) amino) -4-methylbenzamide .
In some embodiments, R1 is independently selected from hydrogen, -CH3,
-CH2CH3,-CH2OH, CN, or R1 and R3 are taken together to form =0.
In some embodiments, R 1 and R 2 are taken together to form carbocyclyl or heterocyclyl, either of which is optionally substituted with up to 3 substituents independently selected from halo. Ci-C4 alkyl, C1-C4 haloalkyl, C1-C4 alkoxy, -CN, =0, -OH, and -C(0)Ci-C4 alkyl.
In some embodiments, R is -(C C4 alkyl) optionally substituted with fluoro or -OH; -(C0-C4 alkylene)-0-(Ci-C4 alkyl), -(C0-C2 alkylene)-N(R6)-(Ci-C6 alkyl), -(C0-C2 alkylene)-Q, and -0-(Co-C2 alkylene)-Q, wherein Q is optionally substituted with up to 3 substituents independently selected from Q-C4 alkyl, Q-C4 haloalkyl, Q-C4 alkoxy, =0, -C(0)-C1-C4 alkyl, -CN, and halo. In one aspect of these embodiments, Q is selected from pyridinyl,
tetrahydrofuranyl, cyclobutyl, cyclopropyl, phenyl, pyrazolyl, morpholinyl and oxetanyl, wherein Q is optionally substituted with up to 2 substituents independently selected from Q-C4 alkyl, Q-C4 haloalkyl, =0, fluoro, chloro, and bromo. In another aspect of these embodiments, Q is selected from pyridinyl, tetrahydrofuranyl, cyclobutyl, cyclopropyl, phenyl, pyrazolyl, morpholinyl and oxetanyl, wherein Q is optionally substituted with up to 2 substituents independently selected from -CH and =0.
In some embodiments, R 1 and R 2 are taken together to form cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, tetrahydrofuranyl, tetrahydropyranyl, oxetanyl, bicyclo[2.2.1]heptanyl, oxobicyclo[3.1.0]hexanyl, azetidinyl, phenyl and pyridinyl, any of which is optionally substituted with up to 2 substituents independently selected from Q-C4 alkyl, Q-C4 alkoxy, C3-C6 cycloalkyl, -OH, -C(0)CH3, fluoro, and chloro.
In some embodiments, ring A is an optionally substituted 6-membered monocyclic aryl. In some embodiments, ring A is an optionally substituted 5-6 membered heteroaryl. In some embodiments, ring A is an optionally substituted 6 membered heteroaryl.
In some embodiments, ring A is selected from phenyl, pyrazolyl, oxazolyl, isoxazolyl, pyridinyl, pyrimidinyl, pyrazinyl, and thiazolyl, wherein ring A is optionally substituted with up to two substituents independently selected from halo, -CrC4 alkyl, -CrC4 haloalkyl, -CrC4 hydroxyalkyl, -NH-S(0)2-(Ci-C4 alkyl), -S(0)2NH(Ci-C4 alkyl), -CN, -S(0)2-(Ci-C4 alkyl), C1-C4 alkoxy, -NH(Ci-C4 alkyl), -OH, -OCF3, -CN, -NH2, -C(0)NH2, -C(0)NH(Ci-C4 alkyl), -C(0)-N(C1-C4 alkyl)2, and cyclopropyl optionally substituted with OH.
In some embodiments, ring A is selected from phenyl, pyrazolyl, oxazolyl, isoxazolyl, pyridinyl, pyrimidinyl, pyrazinyl, and thiazolyl, wherein ring A is optionally substituted with up to two substituents independently selected from halo, -C1-C4 alkyl, -C1-C4 haloalkyl, -C1-C4 hydroxyalkyl, -NH-S(0)2-(Ci-C4 alkyl), -S(0)2NH(Ci-C4 alkyl), -CN, -S(0)2-(Ci-C4 alkyl), CrC4 alkoxy, -NH(C C4 alkyl), -OH, -CN, and -NH2.
In some embodiments, ring B is selected from phenyl, pyrazolyl, oxazolyl, isoxazolyl, thiazolyl, pyridinyl, pyrimidinyl, pyridazinyl, and pyrazinyl, wherein ring B is optionally substituted with up to two substituents independently selected from halo, -C1-C4 alkyl, -C2-C4 alkynyl, -CrC4 haloalkyl, -CrC4 hydroxyalkyl, C3-C6 cycloalkyl, -(C0-C2 alkylene)-0-C1-C4 alkyl, -0-(CrC4 alkylene)-C3-C6 cycloalkyl, -NH-S(0)2-(Ci-C4 alkyl), -S(0)2NH(Ci-C4 alkyl), -S(0)2-NH-(C3-C6 cycloalkyl), -S(0)2-(saturated heterocyclyl),-CN, -S(0)2-(Ci-C4 alkyl), -NH(Ci-C4 alkyl), -N(C C4 alkyl)2, -OH, C(0)-0-(Ci-C4 alkyl), saturated heterocyclyl, and -NH2.
In another embodiment the compound is a compound having Structural Formula II:
Figure imgf000018_0001
(II), or a pharmaceutically acceptable salt thereof, wherein:
Ring A' is selected from phenyl and pyridin-2-yl, wherein ring A' is optionally substituted with one or two substituents independently selected from chloro, fluoro, -CF , -CHF2, -CH3, -CH2CH3, -CF2CH3, -OH, -OCH3, -OCH2CH3, -NH2, -NH(CH3), and -N(CH3)2;
Ring B' is selected from pyridin-3-yl, pyridin-4-yl, isoxazoly-4-yl, isoxazol-3-yl, thiazol-5-yl, pyrimidin-5-yl and pyrazol-4-yl, wherein ring B' is optionally substituted with one to two substituents independently selected from halo; -CN; -OH; CrC4 alkyl optionally substituted with halo, CN or -OH; -S(0)2-Ci-C4 alkyl; -S(0)-Ci-C4 alkyl; -S(0)2-NH-Ci-C4 alkyl; -S(0)2-N(Ci-C4 alkyl)2; -S(0)2-azetidin-l-yl; -O-C1-C4 alkyl; -CH2-0-CH3,
morpholin-4-yl, cyclopropyl, -S(0)2-NH-cyclopropyl; -C(0)-0-CH ; and
-C(Rla)(R2a)(R3a) is selected from Ci-C6 alkyl optionally substituted with halo or -OH; -(Co-Ci alkylene)-cycloalkyl, wherein the alkylene is optionally substituted with methyl and the cycloalkyl is optionally substituted with halo, -OCH3 or methyl; saturated heterocyclyl optionally substituted with halo or methyl; -C(0)-0-C1-C6 alkyl; -C(0)-(Co-C1 alkylene)-cyclopropyl; and C(0)-benzyl.
In certain embodiments of Formula II, ring A' is selected from 2-chlorophenyl, 2- fluorophenyl, 2-methoxyphenyl, 3-hydroxyphenyl, 6-aminopyridin-2-yl, 6-chloropyridin-2-yl, 6- trifluoromethylpyridin-2-yl, and phenyl.
In certain embodiments of Formula II, ring B' is selected from 2-(morpholin-4- yl)pyridin-4-yl, 2-dimethylaminopyridin-4-yl, 3-(2-methyoxyethyl)phenyl, 3,5-difluorophenyl,
3- chlorophenyl, 3-cyanomethylphenyl, 3-cyanophenyl, 3-cyclopropylaminosulfonylphenyl, 3- dimethylaminosulfonylphenyl, 3-ethylsulfonylphenyl, 3-fluorophenyl, 3-methylsulfonylphenyl,
4- fluorophenyl, 5-chloropyridin-3-yl, 5-cyanopyridin-3-yl, 5-cyanopyridin-3-yl, 5-cyanopyridin- 4-yl, 5-fluoropyridin-3-yl, 5-trifluoromethypyridin-3-yl, 6-chloropyridin-4-yl, 6-cyanopyridin-4- yl, 6-cyclopropylpyridin-4-yl, 6-ethoxypyridin-4-yl, 6-fluoropyridin-3-yl, 6-fluoropyridin-4-yl, 6-methylpyridin-4-yl, 6-trifluoromethylpyridin-4-yl, isoxazol-4-yl, phenyl, pyridin-4-yl, and thiazol-5-yl.
In certain embodiments of Formula II, the moiety represented by C(Rla)(R2a)(R3a) is selected from 2-hydroxycyclopentyl, 3-hydroxycyclopentyl, 1-methylcyclopropyl, 2- methylcyclopropyl, 3,3-difluorocyclobutyl, bicycloheptanyl, -(CH2) CH , -CH(CH )-C(CH ) , -CH(CH3)-CH2OCH3, -C(0)-C(CH3)3, -C(0)-OC(CH3)3, -C(0)CH2OH, -C(0)-CH(CH3)2, -C(0)-l-hydroxycyclopropyl, -C(0)-2-pyrrolidinon-5-yl, -C(0)-2-pyrrolyl,
-C(0)CH2OCH(CH3)2, -C(0)-cyclopropyl,-C(0)-CH2-cyclopropyl, -C(0)-OC(CH3)3,
-C(0)CH(CH3)OH, -C(0)-lH-pyrazol-5-yl, -C(0)NHCH2CH3, -CH2CH(CH3)OCH3,
-CH2CH2CH2OCH3, -C(0)-OCH2CH(CH3)2, -CH2CH2-OCH3, -C(0)-OCH2CH3, -C(O)- CH2CH3, -CH(CH3)-CH(CH3)2, -CH2CH(CH3)OH, -CH(CH3)CH2CH3, -CH(CH3)-CH2CH3, -CH(CH3)CH2OH, -CH2C(CH3)3, -CH(CH2OH)CH(CH3)CH3, -CH(CH3)C(CH3)3, -CH2C(CH3)2CH2OH, -CH2CH2OH, -CH2CH(CH3)OH, -CH(CH3)CH2OCH3,
-CH2-CH(CH3)CH2OH,-CH2C(CH3)2OCH3, -CH(C(CH3)3)CH2OH, -CH2C(CH3)2-OH,
CH2C(CH3)3, -CH2CF3, -CH2CH(CH3)2, -CH2CH(CH3)2, -CH2CH2CF3, -CH2CH2OCH2CH3, -CH2CH(CH3)-CH2CH3, -CH2CH2CH(CH3)2, -CHC(CH3)3CH2OH, -CH(CH2CH3)CH2OH, -CH2C(CH3)2OH, -CH2-oxetan-2-yl, -CH2-oxetan-3-yl, -CH2-cyclopropyl, -CH2-cyclobutyl, -CH(CH3)-cyclopropyl, -C(0)-l-methylcyclopropyl, -C(0)-tetrahydrofuran-2-yl, -CH2- tetrahydrofuran-2-yl, -C(0)-tetrahydrofuran-3-yl, -CH2-morpholin-2-yl, -CH2-1- methyltetrahydrofuran-2-yl, cyclobutyl, 3-methoxycyclobutyl, 3-cyclobutanone, cyclohexyl, 4- hydroxycyclohexyl, cyclopentyl, 3-hydroxycyclopentyl, 2-hydroxycyclopentyl, cyclopropyl, ethyl, isopropyl, isobutyl, n-propyl, n-butyl, oxetan-3-yl, oxobicyclohexanyl, tertrahydropyran- 4-yl, 3-oxetanyl, 2-oxetanyl, tetrahydropyran-3-yl, 4,4-difluorocyclohexyl, 4-hydroxycyclohexyl, 3-hydroxycyclohexyl, 2-hydroxycyclohexyl, 3-tetrahydrofuranyl, 1-cyanocyclobutyl, 1- cyanocyclopropyl, 4-methoxycyclobutyl, 3-methyl-oxetan-3-yl, bicyclo[2.2.1]heptanyl, 3- oxabicyclo[3.1.0]hexanyl and 3-cyclohex-2-enonyl.
In certain embodiments of Formula II, the moiety represented by C(Rla)(R2a)(R3a) is selected from 2-hydroxycyclopentyl, 2-methylcyclopropyl, 3,3-difluorocyclobutyl,
bicycloheptanyl, -(CH2)3CH3, -CH(CH3)-C(CH3)3, -CH(CH3)-CH2OCH3, -C(0)-C(CH3)3, -C(0)-CH(CH3)2, -C(0)-cyclopropyl, -C(0)-OC(CH3)3, -C(0)-OCH2CH(CH3)2,
-C(0)-OCH2CH3, -CH(CH3)-CH(CH3)2, -CH(CH3)-CH2CH3, -CH2C(CH3)2CH2OH,
CH2C(CH3)3, -CH2CF3, -CH2CH(CH3)2, -CH2CH(CH3)-CH2CH3, -CH2CH2CH(CH3)2, -CH2- cyclopropyl, cyclobutyl, cyclohexyl, cyclopentyl, cyclopropyl, isopropyl, oxetan-3-yl, oxobicyclohexanyl, tertrahydropyran-4-yl, and tetrahydropyran-3-yl.
In another embodiment the compound is a compound having Structural Formula II:
Figure imgf000020_0001
(II), or a pharmaceutically acceptable salt thereof, wherein: Ring A' is selected from phenyl, pyrimidin-2-yl, pyrimidin-4-yl, pyrimidin-5-yl, oxazol-
4- yl, isoxazol-3-yl, thiazol-2-yl, pyridin-3-yl and pyridin-2-yl, wherein ring A' is optionally substituted with one or two substituents independently selected from 1-propenyl,
-cyclopropyl-OH, chloro, fluoro, -CF3, -CHF2, -CH3, -CH2CH3, -CF2CH3, -S(0)CH3, -S(0)2CH3, -CH2OH, -CH(OH)CH3, -CH(OH)CF3, -OH, -OCH3, -OCF3, -OCH2CH3, -C(0)-NH2, -CH2NH2, -NH2, -NH(CH3), -CN and -N(CH3)2;
Ring B' is selected from phenyl, pyridin-3-yl, pyridin-4-yl, pyridazin-4-yl, isoxazol-4-yl, isoxazol-3-yl, thiazol-5-yl, pyrimidin-5-yl and pyrazol-4-yl, wherein ring B' is optionally substituted with one to two substituents independently selected from halo; -CN; -OH; C C4 alkyl optionally substituted with halo, CN or -OH; -S(0)2-Ci-C4 alkyl; -S(0)-Ci-C4 alkyl;
-S(0)2-NH-Ci-C4 alkyl; -S(0)2-NH-CH2-CF3; -S(0)2-N(Ci-C4 alkyl)2; -S(0)2-azetidin-l-yl; -0-C1-C4 alkyl; -CH2-0-CH , morpholin-4-yl, cyclopropyl, cyclopropyl-C1-C4 alkyl,
cyclopropyl-C1-C4 alkoxy, cyclopropyl-CN, -S(0)2-NH-cyclopropyl; -S(0)2-NH-CH2- cyclopropyl; -C(0)-Ci-C4 alkyl, -C(0)-0-CH3; and
-C(Rla)(R2a)(R3a) is selected from Ci-C6 alkyl optionally substituted with halo, -OCH3, -P(0)3 " or -OH; -(Co-Q alkylene)-cycloalkyl, wherein the alkylene is optionally substituted with methyl and the cycloalkyl is optionally substituted with -OH, -CH2OH, halo, -OCH or methyl; saturated or partially saturated -(Co-Ci alkylene) -heterocyclyl wherein the heterocyclyl is optionally substituted with halo, -S(0)2-CH2-C(0)-Ci-C6 alkyl, -S(0)2-Ci-C6 alkyl, -C(0)-0-Ci- C6 alkyl, -C(0)-N(CH3)2 or methyl; -C(0)-0-Ci-C6 alkyl; -C(O)-(C0-Ci alkylene)-cyclopropyl; and C(0)-benzyl.
In certain embodiments of Formula II, ring A' is selected from 2-chlorophenyl, 2- fluorophenyl, 2-methoxyphenyl, 3-hydroxyphenyl, 3-amidophenyl, 3-methylsulfinylphenyl, 3- methylsulfonylphenyl, 3-(l-methanol)phenyl, 3-methanaminephenyl, 3-methoxy-2-fluorophenyl,
5- methoxy-2-fluorophenyl, 3-hydroxy-2-fluorophenyl, 5-hydroxy-2-fluorophenyl, 5-hydroxy-3- fluorophenyl, 3-methanolphenyl, 3,5-dihydroxyphenyl, 3-trifluoromethyl-5-chlorophenyl, 3-(l- hydoxy-2,2,2-trifluoroethyl)phenyl, 3-(l-hydoxyethyl)phenyl, 3-(l-hydoxycyclopropyl)phenyl, 3-hydroxymethyl-5-phenol, pyridin-2-yl, 3-fluoropyridin-2-yl, 3-cyanopyridin-2-yl, 3,6- difluoropyridin-2-yl, 3-fluoro-6-methoxypyridin-2-yl, 3-fluoro-6-hydroxypyridin-2-yl, 3-fluoro-
6- aminopyridin-2-yl, 4-fluoro-6-aminopyridin-2-yl, 6-propen-l-ylpyridin-2-yl, 6-prop-l- ylpyridin-2-yl, 6-methylaminopyridin-2-yl, 3-fluoro-6-trifluoromethylpyridin-2-yl, 4-chloro-6- aminopyridin-2-yl, 4-fluoro-6-aminopyridin-2-yl, 4-chloro-6-methoxypyridin-2-yl, 6- aminopyridin-3-yl, 2-methoxypyridin-3-yl, 6-aminopyridin-2-yl, 6-chloropyridin-2-yl, 6- trifluoromethylpyridin-2-yl, 6-difluoromethylpyridin-2-yl, 4-(CH2OH)-6-trifluoromethyl- pyridin-2-yl, 4-(CH2OH)-6-chloro-pyridin-2-yl, 6-(l,l-difluoroethyl)-4-fluoropyridin-2-yl, 4- trifluoromethylpyrimidin-2-yl, 4-aminopyrimidin-2-yl, 6-trifluoromethyl-4-aminopyrimidin-2-yl, 4-trifluoromethyl-6-aminopyrimidin-2-yl, 4-aminopyrimidin-2-yl, 2-aminopyrimidin-4-yl, 2- aminopyrimidin-5-yl, 4,6-dichloropyridin-2-yl, 3,5-dichlorophenyl, 2,6-difluorophenyl, 2- methyloxazol-4-yl, 3-methylisoxazol-5-yl, 4-trifluoromethyl-thiazol-2-yl, 4-methylthiazol-2-yl and phenyl.
In certain embodiments of Formula II, ring B' is selected from 2-(morpholin-4- yl)pyridin-4-yl, 2-dimethylaminopyridin-4-yl, 3-(2-methyoxyethyl)phenyl, 3,5-difluorophenyl, 3-chlorophenyl, 3-cyanomethylphenyl, 3-cyanophenyl, 3-(cyclopropylmethyl)phenyl, 3- cyclopropylaminosulfonylphenyl, 3-dimethylaminosulfonylphenyl, 3-ethylsulfonylphenyl, 3- fhiorophenyl, 3-methylsulfonylphenyl, 4-fluorophenyl, 3-(l-hydroxyisopropyl)phenyl, 3- methylsulfonyl-5-chlorophenyl, 3-methylsulfonyl-5-fluorophenyl, 3-(N-2,2,2,- trifluoroethylaminosulfonyl)phenyl, 3-(N-cyclopropyl)benzamide, 5-chloropyridin-3-yl, 5- cyanopyridin-3-yl, 5-cyanopyridin-3-yl, 5-cyanopyridin-4-yl, 5-fhioropyridin-3-yl, 2-(l- hydroxyisopropyl)pyridin-4-yl, 5-trifluoromethypyridin-3-yl, 2-trifluoromethylpyridin-4-yl, 2- difluoromethylpyridin-4-yl, 2-chloropyridin-4-yl, 6-chloropyridin-4-yl, 6-cyanopyridin-4-yl, 2- cyanopyridin-4-yl, 6-cyclopropylpyridin-4-yl, 6-ethoxypyridin-4-yl, 6-fluoropyridin-3-yl, 2- fluoropyridin-4-yl, 5,6-difluoropyridin-3-yl, 6-fluoropyridin-4-yl, 6-methylpyridin-4-yl, 2- difluoromethylpyridin-4-yl, 6-trifluoromethylpyridin-4-yl, 2-( 1 -methoxycyclopropyl)pyridin-4- yl, 2-cyclopropylpyridin-4-yl, 2-(propan-l-one)pyridin-4-yl, 2-(l-methylcyclopropyl)pyridin-4- yl, 2-(l-cyanocyclopropyl)pyridin-4-yl, 2-(l-cyanoisopropyl)pyridin-4-yl, isoxazol-4-yl, phenyl, pyridin-4-yl, picolinat-2-yl, pyrimidin-5-yl, 1 -prop yip yrazol-4-yl, 6-methyl-pyridazin-4-yl, and thiazol-5-yl.
In certain embodiments of Formula II, the moiety represented by C(Rla)(R2a)(R3a) is selected from 2-hydroxycyclopentyl, 3-hydroxycyclopentyl, 1-methylcyclopropyl, 2- methylcyclopropyl, 3,3-difluorocyclobutyl, bicycloheptanyl, -(CH2)3CH3, -CH(CH3)-C(CH3)3, -CH(CH3)-CH2OCH3, -C(0)-C(CH3)3, -C(0)-OC(CH3)3, -C(0)CH2OH, -C(0)-CH(CH3)2, -C(0)-l-hydroxycyclopropyl, -C(0)-2-pyrrolidinon-5-yl, -C(0)-2-pyrrolyl,
-C(0)CH2OCH(CH3)2, -C(0)-cyclopropyl,-C(0)-CH2-cyclopropyl, -C(0)-OC(CH3)3,
-C(0)CH(CH3)OH, -C(0)-lH-pyrazol-5-yl, -C(0)NHCH2CH3, -CH2CH(CH3)OCH3,
-CH2CH2CH2OCH3, -C(0)-OCH2CH(CH3)2, -CH2CH2-OCH3, -C(0)-OCH2CH3, -C(O)- CH2CH3, -CH(CH3)-CH(CH3)2, -CH2CH(CH3)OH, -CH(CH3)CH2CH3, -CH2C(CH3)2OH, -CH(CH3)-CH2CH3, -CH(CH3)CH2OH, -CH2C(CH3)3, -CH(CH2OH)CH(CH3)CH3,
-CH(CH3)C(CH3)3, -CH2C(CH3)2-CH2OH, -CH2CH2OH, -CH2CH(CH3)OH,
-CH(CH3)CH2OCH3, -CH2-CH(CH3)CH2OH,-CH2C(CH3)2OCH3, -C(CH3)2CH2OH,
-CH2CH(CH3)OCH3, -CH(CH3)CH(CH3)OH, -CH2CH(CH3)CH2OH, -CH(C(CH3)3)CH2OH, CH(CH3)C(CH3)2OH, -CH2C(CH3)2-OH, CH2C(CH3)3, -CH2CF3, -CH2CH(CH3)2,
-CH2CH(CH3)2, -CH2CH2CF3, -CH2CH2OCH2CH3, -CH2CH(CH3)-CH2CH3,
-CH2CH2CH(CH3)2, -CH(C(CH3)3)CH2OH, -CH(CH2CH3)CH2OH, -CH2C(CH3)2OH, -CH2- oxetan-2-yl, -CH2-oxetan-3-yl, -CH2-l-methyl-oxetan-3-yl, -CH2-cyclopropyl, -CH2-1- hydroxycyclopropyl, -CH2-cyclobutyl, -CH(CH3)-cyclopropyl, -C(0)-l-methylcyclopropyl, -C(0)-tetrahydrofuran-2-yl, -CH2-tetrahydrofuran-2-yl, -CH2-tetrahydrofuran-3-yl , -C(O)- tetrahydrofuran-3-yl, -CH2-morpholin-2-yl, -CH2-l-methyltetrahydrofuran-2-yl, cyclobutyl, 3- methoxycyclobutyl, 3-cyclobutanone, cyclohexyl, 4-hydroxycyclohexyl, cyclopentyl, 3- hydroxycyclopentyl, 2-hydroxycyclopentyl, cyclopropyl, ethyl, isopropyl, isobutyl, n-propyl, n- butyl, t-butyl, oxetan-3-yl, oxobicyclohexanyl, tetrahydropyran-4-yl, 3-oxetanyl, 2-oxetanyl, tetrahydropyran-3-yl, 4,4-difluorocyclohexyl, 4-hydroxycyclohexyl, 3-hydroxycyclohexyl, 2- hydroxycyclohexyl, 3-tetrahydrofuranyl, 1-cyanocyclobutyl, 1-cyanocyclopropyl, 1- methylcyclopropyl, l-(hydroxymethyl)cyclopropyl, 2-methylcyclopropyl, 2- hydroxycyclopropyl, 4-methoxycyclobutyl, 3-methyl-oxetan-3-yl, bicyclo[2.2.1]heptanyl, 3- oxabicyclo[3.1.0]hex-6-yl, l-(t-butylcarboxylate)piperidin-4-yl, piperidin-4-yl, 1- (methylcarboxylate)piperidin-4-yl, l-(l-ethanone)piperidin-4-yl, l-(methylsulfonyl)piperidin-4- yl, l-methylpyrazol-4-yl, l-methylpyrazol-5-yl, thiazol-5-yl, 7-oxa-bicyclo[2.2.1]hept-2-yl, tetrahydropyran-4-yl, and 3-cyclohex-2-enonyl.
In certain embodiments of Formula II, the moiety represented by C(Rla)(R2a)(R3a) is selected from 2-hydroxycyclopentyl, 2-methylcyclopropyl, 3,3-difluorocyclobutyl, bicycloheptanyl, -(CH2)3CH3, -CH(CH3)-C(CH3)3, -CH(CH3)-CH2OCH3, -C(0)-C(CH3)3, -C(0)-CH(CH3)2, -C(0)-cyclopropyl, -C(0)-OC(CH3)3, -C(0)-OCH2CH(CH3)2,
-C(0)-OCH2CH3, -CH(CH3)-CH(CH3)2, -CH(CH3)-CH2CH3, -CH2C(CH3)2-CH2OH,
-CH2C(OH)(CH3)3, CH2C(CH3)3, -CH2CF3, -CH2CH(CH3)2, -CH2CH(CH3)-CH2CH3,
-CH2CH2CH(CH )2, -CH2-cyclopropyl, cyclobutyl, cyclohexyl, cyclopentyl, cyclopropyl, isopropyl, t-butyl, oxetan-3-yl, oxobicyclohexanyl, tertrahydropyran-4-yl, and tetrahydropyran- 3-yl.
In certain embodiments of Formula II, the moiety represented by C(Rla)(R2a)(R3a) is selected from 2-methylcyclopropyl, -(CH2)3CH3, -CH(CH3)-C(CH3)3, -CH(CH3)-CH2OCH3, -CH(CH3)-CH(CH3)2, -CH(CH3)-CH2CH3, -CH2C(CH3)2-CH2OH, -CH2C(OH)(CH3)3, CH2C(CH3)3, -CH2CF3, -CH2CH(CH3)2, -CH(CH3)2, -CH2CH(CH3)-CH2CH3,
-CH2CH2CH(CH )2, -CH2-cyclopropyl, isopropyl, and t-butyl.
Further embodiments provided herein include combinations of one or more of the particular embodiments set forth above.
In another embodiment, the compound is selected from any one of the compounds set forth in Table 1, below.
Figure imgf000024_0002
Figure imgf000024_0001
Figure imgf000024_0003
Figure imgf000025_0001

Figure imgf000026_0001

Figure imgf000027_0001

Figure imgf000028_0001

Figure imgf000029_0001
Figure imgf000030_0001
Figure imgf000031_0001
Figure imgf000032_0001
31
Figure imgf000033_0001
32
Figure imgf000034_0001
33
Figure imgf000035_0001
Figure imgf000036_0001
Figure imgf000037_0001
Figure imgf000038_0001

Figure imgf000039_0001

Figure imgf000040_0001
Figure imgf000041_0001
Figure imgf000042_0001
Figure imgf000043_0001
Figure imgf000044_0001
43
Figure imgf000045_0001
Figure imgf000046_0001

Figure imgf000047_0001
Figure imgf000048_0001

Figure imgf000049_0001


Figure imgf000051_0001
50
Figure imgf000052_0001
51
Figure imgf000053_0001
52
Figure imgf000054_0001
53
Figure imgf000055_0001
54
Figure imgf000056_0001
55
Figure imgf000057_0001

Figure imgf000058_0001

Figure imgf000059_0001

Figure imgf000060_0001

Figure imgf000061_0001
60
Figure imgf000062_0001
61
Figure imgf000063_0001
62
Figure imgf000064_0001
63
Figure imgf000065_0001
64
Figure imgf000066_0001
65
Figure imgf000067_0001
66
Figure imgf000068_0001

Figure imgf000069_0001

Figure imgf000070_0001
 Included herein are also methods for making compounds of Formula I or a compound of
of the embodiments described herein comprising reacting
Figure imgf000071_0001
omprise step ( 1) reacting
step (2) reacting
Figure imgf000071_0002
. In other embodiments, the preceding methods comprise ; step (2) reacting tep (3) reacting
Figure imgf000071_0003
Also included are methods for making compounds of Formula I or a compound of any embodiments described herein comprising reacting with
some embodiments, omprise step (1) reacting
CI ; and step (2) reacting
Figure imgf000072_0001
. In other embodiments, the preceding methods wherein R
), comprise step (1) reacting and step (2) reacting
Figure imgf000072_0002
Also included are methods for making compounds of Formula I or a compound of any
one of the embodiments described herein comprising
Figure imgf000073_0001
wlth
( A)-B(OH)2
some embodiments, the preceding methods comprise step (1) reacting
; and step (2) reacting
Figure imgf000073_0002
Also included are methods for making compounds of Form I or a compound of any
one of the embodiments described herein comprising reacting
Figure imgf000073_0003
( B J— halide
in some embodiments, the preceding methods comprise step (1) reacting
step (2) reacting
Figure imgf000073_0004
with <— ^ Also included are methods for making compounds of Formula I or a compound of any
one of the embodiments described herein comprising reacting
Figure imgf000074_0001
with
Figure imgf000074_0002
. In some embodiments, the preceding methods comprise step (1) reacting
and step (2) reacting
Figure imgf000074_0003
with . In other embodiments, the preceding methods
comprise step (1) converting
Figure imgf000074_0004
to ; step (2) reacting
; and step (3) reacting
Figure imgf000074_0005
The compounds of one aspect of this invention may contain one or more asymmetric centers and thus occur as racemates, racemic mixtures, scalemic mixtures, and diastereomeric mixtures, as well as single enantiomers or individual stereoisomers that are substantially free from another possible enantiomer or stereoisomer. The term "substantially free of other stereoisomers" as used herein means a preparation enriched in a compound having a selected stereochemistry at one or more selected stereocenters by at least about 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98%, or 99%. The term "enriched" means that at least the designated percentage of a preparation is the compound having a selected stereochemistry at one or more selected stereocenters. Methods of obtaining or synthesizing an individual enantiomer or stereoisomer for a given compound are known in the art and may be applied as practicable to final compounds or to starting material or intermediates.
In certain embodiments, the compound of Formula I or II is enriched for a structure or structures having a selected stereochemistry at one or more carbon atoms. For example, the compound is enriched in the specific stereoisomer by at least about 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98%, or 99%.
The compounds of Formula I or II may also comprise one or more isotopic substitutions.
1 2 3
For example, H may be in any isotopic form, including H, H (D or deuterium), and H (T or tritium); C may be in any isotopic form, including 12C, 13C, and 14C; O may be in any isotopic form, including 160 and 180; and the like. For example, the compound is enriched in a specific isotopic form of H, C and/or O by at least about 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98%, or 99%.
Unless otherwise indicated when a disclosed compound is named or depicted by a structure without specifying the stereochemistry and has one or more chiral centers, it is understood to represent all possible stereoisomers of the compound.
The compounds of one aspect of this invention may also be represented in multiple tautomeric forms, in such instances, one aspect of the invention expressly includes all tautomeric forms of the compounds described herein, even though only a single tautomeric form may be represented (e.g., alkylation of a ring system may result in alkylation at multiple sites, one aspect of the invention expressly includes all such reaction products; and keto-enol tautomers). All such isomeric forms of such compounds are expressly included herein.
It may be convenient or desirable to prepare, purify, and/or handle a corresponding salt of the active compound, for example, a pharmaceutically-acceptable salt. Examples of
pharmaceutically acceptable salts are discussed in Berge et al., 1977, "Pharmaceutically
Acceptable Salts." J. Pharm. Sci. Vol. 66, pp. 1-19.
For example, if the compound is anionic, or has a functional group which may be anionic (e.g., -COOH may be -COO"), then a salt may be formed with a suitable cation. Examples of suitable inorganic cations include, but are not limited to, alkali metal ions such as Na+ and K+, alkaline earth cations such as Ca2+ and Mg2+, and other cations such as Al3+. Examples of suitable organic cations include, but are not limited to, ammonium ion (i.e., NH4 +) and substituted ammonium ions {e.g., NH3R+, NH2R2+, NHR3+, NR4+). Examples of some suitable substituted ammonium ions are those derived from: ethylamine, diethylamine,
dicyclohexylamine, triethylamine, butylamine, ethylenediamine, ethanolamine, diethanolamine, piperazine, benzylamine, phenylbenzylamine, choline, meglumine, and tromethamine, as well as amino acids, such as lysine and arginine. An example of a common quaternary ammonium ion is N(CH3)4 +.
If the compound is cationic, or has a functional group that may be cationic {e.g., -NH2 may be -NH +), then a salt may be formed with a suitable anion. Examples of suitable inorganic anions include, but are not limited to, those derived from the following inorganic acids:
hydrochloric, hydrobromic, hydroiodic, sulfuric, sulfurous, nitric, nitrous, phosphoric, and phosphorous.
Examples of suitable organic anions include, but are not limited to, those derived from the following organic acids: 2-acetyoxybenzoic, acetic, ascorbic, aspartic, benzoic,
camphorsulfonic, cinnamic, citric, edetic, ethanedisulfonic, ethanesulfonic, fumaric,
glucoheptonic, gluconic, glutamic, glycolic, hydroxymaleic, hydroxynaphthalene carboxylic, isethionic, lactic, lactobionic, lauric, maleic, malic, methanesulfonic, mucic, oleic, oxalic, palmitic, pamoic, pantothenic, phenylacetic, phenylsulfonic, propionic, pyruvic, salicylic, stearic, succinic, sulfanilic, tartaric, toluenesulfonic, and valeric. Mesylates of each compound in Table 1 are explicitly included herein. Examples of suitable polymeric organic anions include, but are not limited to, those derived from the following polymeric acids: tannic acid, carboxymethyl cellulose.
The compounds provided herein therefore include the compounds themselves, as well as their salts, hydrates and their prodrugs, if applicable. The compounds provided herein may be modified and converted to prodrugs by appending appropriate functionalities to enhance selected biological properties, e.g., targeting to a particular tissue. Such modifications (i.e., prodrugs) are known in the art and include those which increase biological penetration into a given biological compartment (e.g., blood, lymphatic system, central nervous system), increase oral availability, increase solubility to allow administration by injection, alter metabolism and alter rate of excretion. Examples of prodrugs include esters (e.g., phosphates, amino acid (e.g., valine) esters), carbamates and other pharmaceutically acceptable derivatives, which, upon administration to a subject, are capable of providing active compounds. Calcium and sodium phosphates of each compound in Table 1, if applicable, are explicitly included herein. Amino acid (e.g., valine) esters of each compound in Table 1, if applicable, are explicitly included herein.
Compositions and routes of administration
The compounds utilized in the methods described herein may be formulated together with a pharmaceutically acceptable carrier or adjuvant into pharmaceutically acceptable compositions prior to be administered to a subject. In another embodiment, such pharmaceutically acceptable compositions further comprise additional therapeutic agents in amounts effective for achieving a modulation of disease or disease symptoms, including those described herein.
The term "pharmaceutically acceptable carrier or adjuvant" refers to a carrier or adjuvant that may be administered to a subject, together with a compound of one aspect of this invention, and which does not destroy the pharmacological activity thereof and is nontoxic when administered in doses sufficient to deliver a therapeutic amount of the compound.
Pharmaceutically acceptable carriers, adjuvants and vehicles that may be used in the pharmaceutical compositions of one aspect of this invention include, but are not limited to, ion exchangers, alumina, aluminum stearate, lecithin, self-emulsifying drug delivery systems (SEDDS) such as d-cc- tocopherol polyethyleneglycol 1000 succinate, surfactants used in pharmaceutical dosage forms such as Tweens or other similar polymeric delivery matrices, serum proteins, such as human serum albumin, buffer substances such as phosphates, glycine, sorbic acid, potassium sorbate, partial glyceride mixtures of saturated vegetable fatty acids, water, salts or electrolytes, such as protamine sulfate, disodium hydrogen phosphate, potassium hydrogen phosphate, sodium chloride, zinc salts, colloidal silica, magnesium trisilicate, polyvinyl pyrrolidone, cellulose-based substances, polyethylene glycol, sodium
carboxymethylcellulose, polyacrylates, waxes, polyethylene-polyoxypropylene-block polymers, polyethylene glycol and wool fat. Cyclodextrins such as α-, β-, and γ-cyclodextrin, or chemically modified derivatives such as hydroxyalkylcyclodextrins, including 2- and
3-hydroxypropyl-P-cyclodextrins, or other solubilized derivatives may also be advantageously used to enhance delivery of compounds of the formulae described herein. The pharmaceutical compositions of one aspect of this invention may be administered orally, parenterally, by inhalation spray, topically, rectally, nasally, buccally, vaginally or via an implanted reservoir, preferably by oral administration or administration by injection. The pharmaceutical compositions of one aspect of this invention may contain any conventional non-toxic pharmaceutically-acceptable carriers, adjuvants or vehicles. In some cases, the pH of the formulation may be adjusted with pharmaceutically acceptable acids, bases or buffers to enhance the stability of the formulated compound or its delivery form. The term parenteral as used herein includes subcutaneous, intracutaneous, intravenous, intramuscular, intraarticular, intraarterial, intrasynovial, intrasternal, intrathecal, intralesional and intracranial injection or infusion techniques.
The pharmaceutical compositions may be in the form of a sterile injectable preparation, for example, as a sterile injectable aqueous or oleaginous suspension. This suspension may be formulated according to techniques known in the art using suitable dispersing or wetting agents (such as, for example, Tween 80) and suspending agents. The sterile injectable preparation may also be a sterile injectable solution or suspension in a non-toxic parenterally acceptable diluent or solvent, for example, as a solution in 1,3-butanediol. Among the acceptable vehicles and solvents that may be employed are mannitol, water, Ringer's solution and isotonic sodium chloride solution. In addition, sterile, fixed oils are conventionally employed as a solvent or suspending medium. For this purpose, any bland fixed oil may be employed including synthetic mono- or diglycerides. Fatty acids, such as oleic acid and its glyceride derivatives are useful in the preparation of injectables, as are natural pharmaceutically-acceptable oils, such as olive oil or castor oil, especially in their polyoxyethylated versions. These oil solutions or suspensions may also contain a long-chain alcohol diluent or dispersant, or carboxymethyl cellulose or similar dispersing agents which are commonly used in the formulation of pharmaceutically acceptable dosage forms such as emulsions and or suspensions. Other commonly used surfactants such as Tweens or Spans and/or other similar emulsifying agents or bioavailability enhancers which are commonly used in the manufacture of pharmaceutically acceptable solid, liquid, or other dosage forms may also be used for the purposes of formulation.
The pharmaceutical compositions of one aspect of this invention may be orally administered in any orally acceptable dosage form including, but not limited to, capsules, tablets, emulsions and aqueous suspensions, dispersions and solutions. In the case of tablets for oral use, carriers which are commonly used include lactose and corn starch. Lubricating agents, such as magnesium stearate, are also typically added. For oral administration in a capsule form, useful diluents include lactose and dried corn starch. When aqueous suspensions and/or emulsions are administered orally, the active ingredient may be suspended or dissolved in an oily phase is combined with emulsifying and/or suspending agents. If desired, certain sweetening and/or flavoring and/or coloring agents may be added.
The pharmaceutical compositions of one aspect of this invention may also be
administered in the form of suppositories for rectal administration. These compositions can be prepared by mixing a compound of one aspect of this invention with a suitable non-irritating excipient which is solid at room temperature but liquid at the rectal temperature and therefore will melt in the rectum to release the active components. Such materials include, but are not limited to, cocoa butter, beeswax and polyethylene glycols.
Topical administration of the pharmaceutical compositions of one aspect of this invention is useful when the desired treatment involves areas or organs readily accessible by topical application. For application topically to the skin, the pharmaceutical composition should be formulated with a suitable ointment containing the active components suspended or dissolved in a carrier. Carriers for topical administration of the compounds of one aspect of this invention include, but are not limited to, mineral oil, liquid petroleum, white petroleum, propylene glycol, polyoxyethylene polyoxypropylene compound, emulsifying wax and water. Alternatively, the pharmaceutical composition can be formulated with a suitable lotion or cream containing the active compound suspended or dissolved in a carrier with suitable emulsifying agents. Suitable carriers include, but are not limited to, mineral oil, sorbitan monostearate, polysorbate 60, cetyl esters wax, cetearyl alcohol, 2-octyldodecanol, benzyl alcohol and water. The pharmaceutical compositions of one aspect of this invention may also be topically applied to the lower intestinal tract by rectal suppository formulation or in a suitable enema formulation.
Topically-transdermal patches are also included in one aspect of this invention.
The pharmaceutical compositions of one aspect of this invention may be administered by nasal aerosol or inhalation. Such compositions are prepared according to techniques well-known in the art of pharmaceutical formulation and may be prepared as solutions in saline, employing benzyl alcohol or other suitable preservatives, absorption promoters to enhance bioavailability, fluorocarbons, and/or other solubilizing or dispersing agents known in the art.
When the compositions of one aspect of this invention comprise a combination of a compound of the formulae described herein and one or more additional therapeutic or prophylactic agents, both the compound and the additional agent should be present at dosage levels of between about 1 to 100%, and more preferably between about 5 to 95% of the dosage normally administered in a monotherapy regimen. The additional agents may be administered separately, as part of a multiple dose regimen, from the compounds of one aspect of this invention. Alternatively, those agents may be part of a single dosage form, mixed together with the compounds of one aspect of this invention in a single composition.
The compounds described herein can, for example, be administered by injection, intravenously, intraarterially, subdermally, intraperitoneally, intramuscularly, or subcutaneously; or orally, buccally, nasally, transmucosally, topically, in an ophthalmic preparation, or by inhalation, with a dosage ranging from about 0.5 to about 100 mg/kg of body weight, alternatively dosages between 1 mg and 1000 mg/dose, every 4 to 120 hours, or according to the requirements of the particular drug. The methods herein contemplate administration of an effective amount of compound or compound composition to achieve the desired or stated effect. Typically, the pharmaceutical compositions of one aspect of this invention will be administered from about 1 to about 6 times per day or alternatively, as a continuous infusion. Such
administration can be used as a chronic or acute therapy. The amount of active ingredient that may be combined with the carrier materials to produce a single dosage form will vary depending upon the host treated and the particular mode of administration. A typical preparation will contain from about 5% to about 95% active compound (w/w). Alternatively, such preparations contain from about 20% to about 80% active compound.
Lower or higher doses than those recited above may be required. Specific dosage and treatment regimens for any particular subject will depend upon a variety of factors, including the activity of the specific compound employed, the age, body weight, general health status, sex, diet, time of administration, rate of excretion, drug combination, the severity and course of the disease, condition or symptoms, the subject's disposition to the disease, condition or symptoms, and the judgment of the treating physician. Upon improvement of a subject's condition, a maintenance dose of a compound, composition or combination of one aspect of this invention may be administered, if necessary. Subsequently, the dosage or frequency of administration, or both, may be reduced, as a function of the symptoms, to a level at which the improved condition is retained when the symptoms have been alleviated to the desired level. Subjects may, however, require intermittent treatment on a long-term basis upon any recurrence of disease symptoms.
The pharmaceutical compositions described above comprising a compound of Structural Formula I or II or a compound described in any one of the embodiments herein, may further comprise another therapeutic agent useful for treating cancer.
Methods of Use
The inhibitory activities of the compounds provided herein against IDH2 mutants (e.g., IDH2R140Q and IDH2R172K) can be tested by methods described in Example 12 or analogous methods.
Provided is a method for inhibiting a mutant IDH2 activity comprising contacting a subject in need thereof with a compound of Structural Formula I or II, a compound described in any one of the embodiments herein, or a pharmaceutically acceptable salt thereof. In one embodiment, the cancer to be treated is characterized by a mutant allele of IDH2 wherein the IDH2 mutation results in a new ability of the enzyme to catalyze the NAPH-dependent reduction of a-ketoglutarate to R(-)-2-hydroxyglutarate in a subject. In one aspect of this embodiment, the mutant IDH2 has an R140X mutation. In another aspect of this embodiment, the R140X mutation is a R140Q mutation. In another aspect of this embodiment, the R140X mutation is a R140W mutation. In another aspect of this embodiment, the R140X mutation is a R140L mutation. In another aspect of this embodiment, the mutant IDH2 has an R172X mutation. In another aspect of this embodiment, the R172X mutation is a R172K mutation. In another aspect of this embodiment, the R172X mutation is a R172G mutation.
Also provided are methods of treating a cancer characterized by the presence of a mutant allele of IDH2 comprising the step of administering to subject in need thereof (a) a compound of Structural Formula I or II, a compound described in any one of the embodiments herein, or a pharmaceutically acceptable salt thereof, or (b) a pharmaceutical composition comprising (a) and a pharmaceutically acceptable carrier. In one embodiment, the cancer to be treated is characterized by a mutant allele of IDH2 wherein the IDH2 mutation results in a new ability of the enzyme to catalyze the
NAPH-dependent reduction of a-ketoglutarate to R(-)-2-hydroxyglutarate in a patient. In one aspect of this embodiment, the mutant IDH2 has an R140X mutation. In another aspect of this embodiment, the R140X mutation is a R140Q mutation. In another aspect of this embodiment, the R140X mutation is a R140W mutation. In another aspect of this embodiment, the R140X mutation is a R140L mutation. In another aspect of this embodiment, the mutant IDH2 has an R172X mutation. In another aspect of this embodiment, the R172X mutation is a R172K mutation. In another aspect of this embodiment, the R172X mutation is a R172G mutation. A cancer can be analyzed by sequencing cell samples to determine the presence and specific nature of (e.g., the changed amino acid present at) a mutation at amino acid 140 and/or 172 of IDH2.
Without being bound by theory, applicants believe that mutant alleles of IDH2 wherein the IDH2 mutation results in a new ability of the enzyme to catalyze the NAPH-dependent reduction of a-ketoglutarate to R(-)-2-hydroxyglutarate, and in particular R140Q and/or R172K mutations of IDH2, characterize a subset of all types of cancers, without regard to their cellular nature or location in the body. Thus, the compounds and methods of one aspect of this invention are useful to treat any type of cancer that is characterized by the presence of a mutant allele of IDH2 imparting such acitivity and in particular an IDH2 R140Q and/or R172K mutation.
In one aspect of this embodiment, the efficacy of cancer treatment is monitored by measuring the levels of 2HG in the subject. Typically levels of 2HG are measured prior to treatment, wherein an elevated level is indicated for the use of the compound of Formula I or II or a compound described in any one of the embodiments described herein to treat the cancer. Once the elevated levels are established, the level of 2HG is determined during the course of and/or following termination of treatment to establish efficacy. In certain embodiments, the level of 2HG is only determined during the course of and/or following termination of treatment. A reduction of 2HG levels during the course of treatment and following treatment is indicative of efficacy. Similarly, a determination that 2HG levels are not elevated during the course of or following treatment is also indicative of efficacy. Typically, the these 2HG measurements will be utilized together with other well-known determinations of efficacy of cancer treatment, such as reduction in number and size of tumors and/or other cancer- associated lesions, improvement in the general health of the subject, and alterations in other biomarkers that are associated with cancer treatment efficacy.
2HG can be detected in a sample by LC/MS. The sample is mixed 80:20 with methanol, and centrifuged at 3,000 rpm for 20 minutes at 4 degrees Celsius. The resulting supernatant can be collected and stored at -80 degrees Celsius prior to LC-MS/MS to assess 2-hydroxyglutarate levels. A variety of different liquid chromatography (LC) separation methods can be used. Each method can be coupled by negative electrospray ionization (ESI, -3.0 kV) to triple-quadrupole mass spectrometers operating in multiple reaction monitoring (MRM) mode, with MS parameters optimized on infused metabolite standard solutions. Metabolites can be separated by reversed phase chromatography using 10 mM tributyl- amine as an ion pairing agent in the aqueous mobile phase, according to a variant of a previously reported method (Luo et al. J Chromatogr A 1147, 153-64, 2007). One method allows resolution of TCA metabolites: t = 0, 50% B; t = 5, 95% B; t= 7, 95% B; t= 8, 0% B, where B refers to an organic mobile phase of 100% methanol. Another method is specific for 2-hydroxyglutarate, running a fast linear gradient from 50% -95% B (buffers as defined above) over 5 minutes. A Synergi Hydro-RP, 100mm x 2 mm, 2.1 μιη particle size (Phenomonex) can be used as the column, as described above. Metabolites can be quantified by comparison of peak areas with pure metabolite standards at known concentration. Metabolite flux studies from 13 C-glutamine can be performed as described, e.g., in Munger et al. Nat Biotechnol 26, 1179-86, 2008.
In one embodiment 2HG is directly evaluated.
In another embodiment a derivative of 2HG formed in process of performing the analytic method is evaluated. By way of example such a derivative can be a derivative formed in MS analysis. Derivatives can include a salt adduct, e.g., a Na adduct, a hydration variant, or a hydration variant which is also a salt adduct, e.g., a Na adduct, e.g., as formed in MS analysis.
In another embodiment a metabolic derivative of 2HG is evaluated. Examples include species that build up or are elevated, or reduced, as a result of the presence of 2HG, such as glutarate or glutamate that will be correlated to 2HG, e.g., R-2HG.
Exemplary 2HG derivatives include dehydrated derivatives such as the compounds provided below or a salt adduct thereof:
Figure imgf000084_0001
HO' ΌΗ , and
In one embodiment the cancer is a tumor wherein at least 30, 40, 50, 60, 70, 80 or 90% of the tumor cells carry an IDH2 mutation, and in particular an IDH2 R140Q, R140W, or R140L and/or R172K or R172G mutation, at the time of diagnosis or treatment.
In another embodiment, one aspect of the invention provides a method of treating a cancer selected from glioblastoma (glioma), myelodysplastic syndrome (MDS),
myeloproliferative neoplasm (MPN), acute myelogenous leukemia (AML), sarcoma, melanoma, non-small cell lung cancer, chondrosarcoma, cholangiocarcinomas or angioimmunoblastic lymphoma in a patient by administering to the patient a compound of Formula I or Formula II in an amount effective to treat the cancer. In a more specific embodiment the cancer to be treated is glioma, myelodysplastic syndrome (MDS), myeloproliferative neoplasm (MPN), acute myelogenous leukemia (AML), melanoma, chondrosarcoma, or angioimmunoblastic non- Hodgkin's lymphoma (NHL).
2HG is known to accumulate in the inherited metabolic disorder 2-hydroxyglutaric aciduria. This disease is caused by deficiency in the enzyme 2-hydroxyglutarate dehydrogenase, which converts 2HG to a-KG (Struys, E. A. et al. Am J Hum Genet 76, 358-60 (2005)). Patients with 2-hydroxyglutarate dehydrogenase deficiencies accumulate 2HG in the brain as assessed by MRI and CSF analysis, develop leukoencephalopathy, and have an increased risk of developing brain tumors (Aghili, M., Zahedi, F. & Rafiee, J Neurooncol 91, 233-6 (2009); Kolker, S., Mayatepek, E. & Hoffmann, G. F. Neuropediatrics 33, 225-31 (2002); Wajner, M., Latini, A., Wyse, A. T. & Dutra-Filho, C. S. J Inherit Metab Dis 27, 427-48 (2004)). Furthermore, elevated brain levels of 2HG result in increased ROS levels (Kolker, S. et al. Eur J Neurosci 16, 21-8 (2002); Latini, A. et al. Eur J Neurosci 17, 2017-22 (2003)), potentially contributing to an increased risk of cancer. The ability of 2HG to act as an NMDA receptor agonist may contribute to this effect (Kolker, S. et al. Eur J Neurosci 16, 21-8 (2002)). 2HG may also be toxic to cells by competitively inhibiting glutamate and/or aKG utilizing enzymes. These include
transaminases which allow utilization of glutamate nitrogen for amino and nucleic acid biosynthesis, and aKG-dependent prolyl hydroxylases such as those which regulate Hif 1-alpha levels.
Thus, according to another embodiment, one aspect of the invention provides a method of treating 2-hydroxyglutaric aciduria, particularly D-2-hydroxyglutaric aciduria, in a patient by administering to the patient a compound of Structural Formula I or II or a compound described in any one of the embodiments described herein.
Treatment methods described herein can additionally comprise various evaluation steps prior to and/or following treatment with a compound of Structural Formula I or II or a compound described in any one of the embodiments described herein.
In one embodiment, prior to and/or after treatment with a compound of Structural Formula I or II or a compound described in any one of the embodiments described herein, the method further comprises the step of evaluating the growth, size, weight, invasiveness, stage and/or other phenotype of the cancer.
In one embodiment, prior to and/or after treatment with a compound of Formula I or II or a compound described in any one of the embodiments described herein, the method further comprises the step of evaluating the IDH2 genotype of the cancer. This may be achieved by ordinary methods in the art, such as DNA sequencing, immuno analysis, and/or evaluation of the presence, distribution or level of 2HG.
In one embodiment, prior to and/or after treatment with a compound of Formula I or II or a compound described in any one of the embodiments described herein, the method further comprises the step of determining the 2HG level in the subject. This may be achieved by spectroscopic analysis, e.g., magnetic resonance-based analysis, e.g., MRI and/or MRS measurement, sample analysis of bodily fluid, such as serum or spinal cord fluid analysis, or by analysis of surgical material, e.g., by mass-spectroscopy.
Combination therapies
In some embodiments, the methods described herein comprise the additional step of co-administering to a subject in need thereof a second therapy e.g., an additional cancer therapeutic agent or an additional cancer treatment. Exemplary additional cancer therapeutic agents include for example, chemotherapy, targeted therapy, antibody therapies, immunotherapy, and hormonal therapy. Additional cancer treatments include, for example: surgery, and radiation therapy. Examples of each of these treatments are provided below.
The term "co-administering" as used herein with respect to an additional cancer therapeutic agents means that the additional cancer therapeutic agent may be administered together with a compound of one aspect of this invention as part of a single dosage form (such as a composition of one aspect of this invention comprising a compound of one aspect of the invention and an second therapeutic agent as described above) or as separate, multiple dosage forms. Alternatively, the additional cancer therapeutic agent may be administered prior to, consecutively with, or following the administration of a compound of one aspect of this invention. In such combination therapy treatment, both the compounds of one aspect of this invention and the second therapeutic agent(s) are administered by conventional methods. The administration of a composition of one aspect of this invention, comprising both a compound of one aspect of the invention and a second therapeutic agent, to a subject does not preclude the separate administration of that same therapeutic agent, any other second therapeutic agent or any compound of one aspect of this invention to said subject at another time during a course of treatment. The term "co-administering" as used herein with respect to an additional cancer treatment means that the additional cancer treatment may occur prior to, consecutively with, concurrently with or following the administration of a compound of one aspect of this invention.
In some embodiments, the additional cancer therapeutic agent is a chemotherapy agent. Examples of chemotherapeutic agents used in cancer therapy include, for example,
antimetabolites (e.g., folic acid, purine, and pyrimidine derivatives), alkylating agents (e.g., nitrogen mustards, nitrosoureas, platinum, alkyl sulfonates, hydrazines, triazenes, aziridines, spindle poison, cytotoxic agents, topoisomerase inhibitors and others), and hypomethylating agents (e.g. , decitabine (5-aza-deoxycytidine), zebularine, isothiocyanates, azacitidine (5- azacytidine), 5-flouro-2'-deoxycytidine, 5,6-dihydro-5-azacytidine and others). Exemplary agents include Aclarubicin, Actinomycin, Alitretinoin, Altretamine, Aminopterin,
Aminolevulinic acid, Amrubicin, Amsacrine, Anagrelide, Arsenic trioxide, Asparaginase, Atrasentan, Belotecan, Bexarotene, bendamustine, Bleomycin, Bortezomib, Busulfan,
Camptothecin, Capecitabine, Carboplatin, Carboquone, Carmofur, Carmustine, Celecoxib, Chlorambucil, Chlormethine, Cisplatin, Cladribine, Clofarabine, Crisantaspase, Cyclophosphamide, Cytarabine, Dacarbazine, Dactinomycin, Daunorubicin, Decitabine, Demecolcine, Docetaxel, Doxorubicin, Efaproxiral, Elesclomol, Elsamitrucin, Enocitabine, Epirubicin, Estramustine, Etoglucid, Etoposide, Floxuridine, Fludarabine, Fluorouracil (5FU), Fotemustine, Gemcitabine, Gliadel implants, Hydroxycarbamide, Hydroxyurea, Idarubicin, Ifosfamide, Irinotecan, Irofulven, Ixabepilone, Larotaxel, Leucovorin, Liposomal doxorubicin, Liposomal daunorubicin, Lonidamine, Lomustine, Lucanthone, Mannosulfan, Masoprocol, Melphalan, Mercaptopurine, Mesna, Methotrexate, Methyl aminolevulinate, Mitobronitol, Mitoguazone, Mitotane, Mitomycin, Mitoxantrone, Nedaplatin, Nimustine, Oblimersen,
Omacetaxine, Ortataxel, Oxaliplatin, Paclitaxel, Pegaspargase, Pemetrexed, Pentostatin,
Pirarubicin, Pixantrone, Plicamycin, Porfimer sodium, Prednimustine, Procarbazine, Raltitrexed, Ranimustine, Rubitecan, Sapacitabine, Semustine, Sitimagene ceradenovec, Strataplatin, Streptozocin, Talaporfin, Tegafur-uracil, Temoporfin, Temozolomide, Teniposide, Tesetaxel, Testolactone, Tetranitrate, Thiotepa, Tiazofurine, Tioguanine, Tipifarnib, Topotecan,
Trabectedin, Triaziquone, Triethylenemelamine, Triplatin, Tretinoin, Treosulfan, Trofosfamide, Uramustine, Valrubicin, Verteporfin, Vinblastine, Vincristine, Vindesine, Vinflunine,
Vinorelbine, Vorinostat, Zorubicin, and other cytostatic or cytotoxic agents described herein.
Because some drugs work better together than alone, two or more drugs are often given at the same time. Often, two or more chemotherapy agents are used as combination chemotherapy.
In some embodiments, the additional cancer therapeutic agent is a differentiation agent. Such differentiation agent includes retinoids (such as all-trans-retinoic acid (ATRA), 9-cis retinoic acid, lS-ds-retinoic acid (13-cRA) and 4-hydroxy-phenretinamide (4-HPR)); arsenic trioxide; histone deacetylase inhibitors HDACs (such as azacytidine (Vidaza) and butyrates (e.g., sodium phenylbutyrate)); hybrid polar compounds (such as hexamethylene bisacetamide
((HMBA)); vitamin D; and cytokines (such as colony-stimulating factors including G-CSF and GM-CSF, and interferons).
In some embodiments the additional cancer therapeutic agent is a targeted therapy agent. Targeted therapy constitutes the use of agents specific for the deregulated proteins of cancer cells. Small molecule targeted therapy drugs are generally inhibitors of enzymatic domains on mutated, overexpressed, or otherwise critical proteins within the cancer cell. Prominent examples are the tyrosine kinase inhibitors such as Axitinib, Bosutinib, Cediranib, dasatinib, erlotinib, imatinib, gefitinib, lapatinib, Lestaurtinib, Nilotinib, Semaxanib, Sorafenib, Sunitinib, and Vandetanib, and also cyclin-dependent kinase inhibitors such as Alvocidib and Seliciclib. Monoclonal antibody therapy is another strategy in which the therapeutic agent is an antibody which specifically binds to a protein on the surface of the cancer cells. Examples include the anti-HER2/neu antibody trastuzumab (HERCEPTIN®) typically used in breast cancer, and the anti-CD20 antibody rituximab and Tositumomab typically used in a variety of B-cell
malignancies. Other exemplary antibodies include Cetuximab, Panitumumab, Trastuzumab, Alemtuzumab, Bevacizumab, Edrecolomab, and Gemtuzumab. Exemplary fusion proteins include Aflibercept and Denileukin diftitox. In some embodiments, the targeted therapy can be used in combination with a compound described herein, e.g., a biguanide such as metformin or phenformin, preferably phenformin.
Targeted therapy can also involve small peptides as "homing devices" which can bind to cell surface receptors or affected extracellular matrix surrounding the tumor. Radionuclides which are attached to these peptides (e.g., RGDs) eventually kill the cancer cell if the nuclide decays in the vicinity of the cell. An example of such therapy includes BEXXAR®.
In some embodiments, the additional cancer therapeutic agent is an immunotherapy agent. Cancer immunotherapy refers to a diverse set of therapeutic strategies designed to induce the subject's own immune system to fight the tumor. Contemporary methods for generating an immune response against tumors include intravesicular BCG immunotherapy for superficial bladder cancer, and use of interferons and other cytokines to induce an immune response in renal cell carcinoma and melanoma subjects.
Allogeneic hematopoietic stem cell transplantation can be considered a form of immunotherapy, since the donor's immune cells will often attack the tumor in a
graft- versus-tumor effect. In some embodiments, the immunotherapy agents can be used in combination with a compound or composition described herein.
In some embodiments, the additional cancer therapeutic agent is a hormonal therapy agent. The growth of some cancers can be inhibited by providing or blocking certain hormones. Common examples of hormone- sensitive tumors include certain types of breast and prostate cancers. Removing or blocking estrogen or testosterone is often an important additional treatment. In certain cancers, administration of hormone agonists, such as progestogens may be therapeutically beneficial. In some embodiments, the hormonal therapy agents can be used in combination with a compound or a composition described herein.
Other possible additional therapeutic modalities include imatinib, gene therapy, peptide and dendritic cell vaccines, synthetic chlorotoxins, and radiolabeled drugs and antibodies.
EXAMPLES
ABBREVIATIONS
anhy. - anhydrous dt - doublet of triplets
aq. - aqueous CHCI3 - chloroform
min - minute(s) DCM - dichloromethane
mL - milliliter DMF - dimethylformamide
mmol - millimole(s) Et20 - diethyl ether
mol - mole(s) EtOH - ethyl alcohol
MS - mass spectrometry EtOAc - ethyl acetate
NMR - nuclear magnetic resonance MeOH - methyl alcohol
TLC - thin layer chromatography MeCN - acetonitrile
HPLC - high-performance liquid PE - petroleum ether
chromato graphy THF - tetrahydrofuran
Hz - hertz AcOH - acetic acid
δ - chemical shift HC1 - hydrochloric acid
J - coupling constant H2S04 - sulfuric acid
s - singlet NH4C1 - ammonium chloride
d - doublet KOH - potassium hydroxide
t - triplet NaOH - sodium hydroxide
q - quartet K2C03 - potassium carbonate
m - multiplet Na2C03 - sodium carbonate
br - broad TFA - trifluoroacetic acid
qd - quartet of doublets Na2S04 - sodium sulfate
dquin - doublet of quintets NaBH4 - sodium borohydride
dd - doublet of doublets NaHC03 - sodium bicarbonate LiHMDS - lithium hexamethyldisilylamide mide
NaHMDS - sodium hexamethyldisilylamide HOBt - 1-hydroxybenzotriazole
LAH - lithium aluminum hydride HATU - NaBH4 - sodium borohydride 0-(7-azabenzotriazol-l-yl)-N,N,N',N'-tetra- LDA - lithium diisopropylamide methyluronium
Et3N - triethylamine BINAP - DMAP - 4-(dimethylamino)pyridine ' -bis(diphenylphosphanyl)- 1, 1 ' -binaphth DIPEA - N,N-diisopropylethylamine
NH4OH - ammonium hydroxide
EDCI -
1 -ethyl- 3 - (3 -dimethylaminopropyl)carb odii
In the following examples, reagents were purchased from commercial sources (including Alfa, Acros, Sigma Aldrich, TCI and Shanghai Chemical Reagent Company), and used without further purification. Nuclear magnetic resonance (NMR) spectra were obtained on a Brucker AMX-400 NMR (Brucker, Switzerland). Chemical shifts were reported in parts per million (ppm, δ) downfield from tetramethylsilane. Mass spectra were run with electrospray ionization (ESI) from a Waters LCT TOF Mass Spectrometer (Waters, USA).
For exemplary compounds disclosed in this section, the specification of a stereoisomer (e.g., an (R) or (S) stereoisomer) indicates a preparation of that compound such that the compound is enriched at the specified stereocenter by at least about 90%, 95%, 96%, 97%, 98%, or 99%. The chemical name of each of the exemplary compound described below is generated by ChemDraw software.
Example 1. Preparation of Compounds of Formula I Wherein Ring A is Phenyl, and
-C(R )(R )(R ) is Isopropyl. The compounds of this Example are prepared by general Scheme 1, set forth below.
Figure imgf000091_0001
Formula I
Example 1, step 1: Preparation of 2,4-dichloro-6-phenyl-l,3,5-triazine (2). To a solution of 2,4,6-trichloro-[l,3,5]triazine (1, 120 g, 0.652 mol) in anhydrous THF (1200 mL) was added phenylmagnesium bromide (217 mL, 0.651 mol, 3 M in ether) dropwise at -10 to -0°C under N2 protection. After the addition, the mixture was warmed to room temperature and stirred for 2 hrs. The reaction was cooled to 0°C and quenched by addition of saturated NH4C1 (200 mL), then extracted with ethyl acetate. The organic layer was dried, concentrated and purified via column chromatography (eluted with petroleum ether) to afford 2,4-dichloro-6-phenyl-l,3,5-triazine as a white solid. 1H NMR (CDC13) δ 7.51-7.55 (m, 2H), 7.64-7.67 (m, 1H), 8.49-8.63 (m, 2H).
Example 1, step 2: Preparation of 4-chloro-N-isopropyl-6-phenyl-l,3,5-triazin-2-amine (3). To a solution of 2,4-dichloro-6-phenyl-l,3,5-triazine (2; 20 g, 0.089 mol) in anhydrous THF (150 mL) was added dropwise a solution of isopropylamine (5.25 g, 0.089 mol) in THF (10 mL) at room temperature via syringe under N2. After the addition, the mixture was stirred at room temperature under N2 for 16 hrs. The reaction was quenched by water (150 mL) and extracted with ethyl acetate. The organic layer was dried, concentrated and purified via Si02 chromatography to afford 4-chloro-N-isopropyl-6-phenyl-l,3,5-triazin-2-amine (3) as white solid.
1H NMR (CDC13) δ 1.17-1.24 (m, 6H), 4.16-4.35 (m, 1H), 5.46-5.54 (m, 1H), 7.18-7.50 (m, 3H0, 8.31 (dd, Ji =8.4 Hz, J2 = 34.4 Hz, 2H).
Example 1, Step 3 (Procedure A). Preparation of Compound 178 - N-(3-Fluoro-phenyl)-N'-isopropyl-6-phenyl-[l,3,5]triazine-2,4-diamine. A mixture of
(4-chloro-6-phenyl-[l,3,5]triazin-2-yl)-isopropyl-amine (3; 200 mg, 0.806 mmol) and
3-fluoro-phenylamine (135 mg, 1.215 mmol) in anhydrous THF was stirred at room temperature for 16 hrs. The reaction was quenched by water and extracted with ethyl acetate. The organic layer was washed with brine, dried over Na2S04, concentrated and purified by a standard method to give N-(3-fluoro-phenyl)-N'-isopropyl-6-phenyl-[l,3,5]triazine-2,4-diamine.
Figure imgf000092_0001
1H NMR (METHANOL-d4) δ 8.37-8.33 (m, 2H), 7.87-7.84 (m, 1H), 7.52-7.48 (m, 5H), 7.27-7.25 (m, 1H), 6.73-6.69 (m, 1H), 4.24 (m, 1H), 1.16 (d, J = 6.4 Hz, 6H). LC-MS: m/z 323.9 (M+H)+. Other compounds produced by Step 3, Procedure A of this example using the appropriate reagent 4 are set forth below.
Compound 195 - 2-isopropyl-I^-(3-(methoxymethyl)phenyl)-6-phenyl-l,3,5-triazine-2,4-diamine
Figure imgf000092_0002
1H NMR (METHANOL-d ) 8.40-8.34 (m, 2H) 7.99-7.83 (m, 1H), 7.62-7.60 (m, 1H), 7.53-7.44 (m, 3H), 7.31-7.27 (m, 1H), 7.00-6.99 (m, 1H), 4.48 (s,2H) 4.29-4.27 (m, 1H), 3.41 (s, 3H), 1.16 (d, J = 6.8 Hz, 6H). LC-MS: m/z 350.3 (M+H)+.
(3-(4-(isopropylamino)-6-phenyl-l,3,5-triazin-2-ylamino)phenyl)acetonitrile
Figure imgf000092_0003
1H NMR (METHANOL-d ) 8.42-8.38 (m, 2H) 8.18-8.11 (m, 1H), 7.61-7.60 (m, 1H), 7.52-7.45 (m, 3H), 7.35-7.31 (m, 1H), 7.02-7.00 (m, 1H), 4.34 (m, 1H), 3.92 (s, 2H), 1.16 (d, J = 6.8 Hz, 6H). LC-MS: m/z 345.2 (M+H)+.
Compound 201 - 2-(3-(4-(isopropylamino)-6-phenyl-l,3,5-triazin-2-ylamino)phenyl)propan-2-ol
Figure imgf000092_0004
1H NMR (METHANOL-d4) 8.36-8.35 (m, 2H), 8.06-8.01 (m, IH), 7.55-7.44 (m, 4H), 7.29-7.25 (m, IH), 7.20-7.18 (m, IH), 4.46-4.41 (m, IH), 1.58 (s, 6H), 1.16 (d, J = 6.8 Hz, 6H). LC-MS: m/z 364.1 (M+H)+.
Compound 204 - -ethyl-3-(4-(isopropylamino)-6-phenyl-l,3,5-triazin-2-ylamino)benzenesulfonamide
Figure imgf000093_0001
1H NMR (METHANOL-d ) δ 8.86-8.64 (m, IH), 8.44-8.38 (m, 2H), 7.82-7.72 (m, IH), 7.53-7.44 (m, 5H), 4.37-4.35 (m, IH), 2.97-2.92 (m, 2H), 1.299-1.282 (d, J = 6.8 Hz, 6H), 1.09-1.05 (t, 3H). LC-MS: m/z 413.1 (M+H)+.
Compound 205 - N2-(3-(ethylsulfonyl)phenyl)-I^ sopropyl-6^henyl-l,3,5-triazine-2,4-diamine
Figure imgf000093_0002
1H NMR (METHANOL-d4) δ 8.81-8.79 (m, IH), 8.28-8.26 (m, 2H), 7.82-7.63 (m, 6H), 4.45-4.42 (m, IH), 3.26-3.23 (m, 2H), 1.386-1.369 (d, J = 6.8 Hz, 6H), 1.27-1.24(t, 3H). LC-MS: m/z 398.0 (M+H)+.
Compound 206 - 2 sopropyl- -(3-(isopropylsulfonyl)phenyl)-6-phenyl-l,3,5-triazine-2,4-diam
Figure imgf000093_0003
1H NMR (METHANOL-d4) δ 9.00-8.97 (m, IH) 8.45-8.39 (m, 2H), 7.78-7.76 (m, IH), 7.58-7.44 (m, 5H), 4.36-4.31 (m, IH), 3.32-3.31 (m, IH), 1.31-1.29 (m, 6H). LC-MS: m/z 412.0 (M+H)+. Compound 341 -
N-cyclopropyl-3-(4-(isopropylamino)-6-phenyl-l,3,5-triazin-2-ylamino)benzenesulfonamid^
Figure imgf000094_0001
1H NMR (METHANOL-d4) δ 8.77-8.72 (m, 1H), 8.24-8.22(m, 2H), 7.67-7.62 (m, 6H), 4.48-4.45 (m, 1H), 2.24-2.16 (m, 1H), 1.378-1.362 (d, J = 6.4 Hz, 6H), 0.53-0.51(m, 4H). LC-MS: m/z 425.3 (M+H)+.
Compound 342 - -butyl-3-(4-(isopropylamino)-6-phenyl-l,3,5-triazin-2-ylamino)benzenesulfonamide
Figure imgf000094_0002
1H NMR (METHANOL-d4) δ 8.88-8.69 (m, 1H), 8.45-8.49 (m, 2H), 7.77-7.70 (m, 1H), 7.53-7.44 (m, 5H), 4.40-4.37(m, 1H), 1.304-1.288 (d, J = 6.4 Hz, 6H), 1.21(s, 9H). LC-MS: m/z 441.3 (M+H)+.
Compound 351 - 2-(4-(isopropylamino)-6-phenyl-l,3,5-triazin-2-ylamino)phenol
Figure imgf000094_0003
1H NMR (METHANOL-d ) δ 8.40-8.32 (m, 2H), 8.00-7.99 (m, 1H), 7.57-7.47 (m, 3H), 6.97-6.87 (m, 3H), 4.45-4.21 (m, 1H), 1.31 (d, J = 6.8 Hz, 6H). LC-MS: m/z 321.9 (M+H).
Example 1, Step 3 (Procedure B). Preparation of Compound 288 -
N2-isopropyl-I^-(2-methylpyridin-4-yl)-6^henyl-l,3,5-triazine-2,4-diamine. To a solution of (4-chloro-6-phenyl-[l,3,5]triazin-2-yl)-isopropyl-amine (3; 150 mg, 0.6 mmol) in DMSO (2 mL) was added 2-methylpyridin-4-amin (78.4 mg, 0.73 mmol), CsF (310 mg, 1.21 mmol) and DIPEA (230 mg, 1.81 mmol). The mixture was stirred at 80°C for 2 h. The mixture was cooled down to rt and filtered to remove the solid. The filtrate was purified by a standard method to give
N 2 -isopropyl-N 4 -(2-methylpyridin-4-yl)-6-phenyl-l,3,5-triazine-2,4-diamine (110 mg, 57.9%).
Figure imgf000095_0001
1H NMR (METHANOL-d4) δ 8.19-8.40 (m, 5H), 7.53-7.58 (m, 3H), 4.30-4.43 (m,lH), 2.66-2.77 (m, 3H), 1.33 (d, J = 4.4 Hz, 6H). LC-MS: m/z 321.1 (M+H)+.
Additional compounds of Formula I were made using the appropriate reagent 4 and following Step 3, Procedure B.
Compound 292 - N2-(3-fluoropyridin-4-yl)-N4-isopropyl-6-phenyl-l,3,5-triazine-2,4-diamine
Figure imgf000095_0002
1H NMR (METHANOL-d4) δ 1.34-1.39 (m, 6H), 4.43-4.51 (m, IH), 7.19-7.25 (m, IH), 7.53-7.65 (m, 3H), 8.53-8.58 (m, 2H), 9.40-9.45 (m, IH), 9.56-9.60 (m, IH). LC-MS: m/z 325.0 (M+H)+. Compound 298 - 2 sopropyl-I^-(2-morpholinopyridin-4-yl)-6^henyl-l,3,5 riazine-2,4-diamine
Figure imgf000095_0003
1H NMR (METHANOL-d ) δ 8.35-8.37 (m, 2H), 7.76-7.90 (m, 2H), 7.51-7.52 (m,3H), 7.45-7.47 (m,lH), 4.23-4.49 (m,lH),3.82-3085 (m, 4H), 3.50-3.51 (m,4H), 1.30 (d, J = 6.4 Hz, 6H).
LC-MS: m/z 392.1 (M+H)+.
Compound 299 - 2-(2-(azetidin-l-yl)pyridin-4-yl)-N4 sopropyl-6-phenyl-l,3,5-tr ^
Figure imgf000095_0004
1H NMR (METHANOL-d4) δ 8.38-8.43 (m, 2H), 7.46-7.74 (m, 5H), 6.88-6.90 (m,lH),
4.21-4.25(m,4H), 2.53-2.56 (m,2H), 1.30 (d, J = 6.4 Hz, 6H). LC-MS: m/z 362.0 (M+H)+.
Example 1, Step 3 (Procedure C). Preparation of Compound 146 - -(6-fluoro-pyridin-3-yl)-N'-isopropyl-6-phenyl-[l,3,5]triazine-2,4-diamine
Figure imgf000096_0001
3 Formula I
A mixture of (4-chloro-6-phenyl-[l,3,5]triazin-2-yl)-isopropyl-amine (3; 400 mg, 1.61 mmol), 6-fluoro-pyridin-3-ylamine (272 mg, 2.43 mmol) Pd(dppf)Cl2 (120 mg, 0.164 mmol) and t-BuONa (310 mg, 3.23 mmol) was stirred at 80°C under N2 for 2 hrs. The mixture was cooled to room temperature and quenched by water, then extracted with ethyl acetate. The organic layer was washed with brine, dried over Na2S04, concentrated and purified by a standard method to give -(6-fluoro-pyridin-3-yl)-N'-isopropyl-6-phenyl-[l,3,5]triazine-2,4-diamine.
Figure imgf000096_0002
1H NMR (METHANOL-d4) δ 8.41-8.39 (m, 2H), 7.91-7.88 (m, 5H), 7.62-7.45 (m, 3H), 5.55-5.20 (m, 1H), 4.44-4.20 (m., 1H), 3.05 (s., 1H), 1.31 (dd, J = 4, 400 MHz, 6H). LC-MS: m/z 384.2 (M+H)+
Additional compounds of Formula 1 in the example that were prepared according to Example 1, Step 3, Procedure C using the appropriate reagent 4 are set forth below.
Compound 177 - -( 4-( isopropylamino )-6-phenyl-l,3,5-triazin-2-ylamino )-N,N-dimethylbenzenesulfonamide
Figure imgf000096_0003
1H NMR (METHANOL-d4) δ 8.99-8.78 (m, IH), 8.39-8.37 (m, 2H), Ί .99-1.91 (m, IH), 7.91-7.65 (m, IH), 7.54-7.38 (m. 5H), 4.41-4.38 (m, IH), 2.71 (s, 6H), 1.293-1.277 (d, J = 6.4 Hz, 6H). LC-MS: m z 413.1 (M+H)+.
(5-fluoropyridin-3-yl)-N4-isopropyl-6-phenyl-l,3,5-triazine-2,4-diamine
Figure imgf000097_0001
IH NMR (METHANOL-d4) δ 8.47-8.15 (m, 5H), 7.52-7.44 (m, 3H), 7.24-7.17 (m, IH), 5.37-5.16 (m, IH), 4.44-4.19 (m., IH), 3.05 (s., IH), 1.16 (dd, J = 4, 400 MHz, 6H). LC-MS: m/z 325.1 (M+H)+
Compound 194 - N2-(5-chloropyridin-3-yl)-I^ sopropyl-6^henyl-l,3,5-triazine-2,4-diamine
Figure imgf000097_0002
IH NMR (METHANOL-d4) δ 8.59-8.25 (m, 5H), 7.52-7.45 (m, 3H), 7.39-7.26 (m, IH), 5.44-5.23 (m, IH), 4.45-4.20 (m., IH), 3.05 (s., IH), 1.31 (dd, J = 4, 400 MHz, 6H). LC-MS: m/z 340.9 (M+H)+
Compound 196 - N2-( 6-fluoropyridin-3-yl)-N4-isopropyl-6-phenyl-l,3,5-triazine-2,4-diamine
Figure imgf000097_0003
1H NMR (METHANOL-d ) δ 8.63-8.57 (m, IH), 8.38-8.35 (m, 3H), 7.51-7.45 (m, 3H), 7.05-7.01 (m. IH), 4.40-4.23 (m, IH), 1.286-1.273 (d, J = 5.2 Hz, 6H). LC-MS: m/z 325.2 (M+H)+.
(4-(isopropylamino)-6-phenyl-l,3,5-triazin-2-ylamino)picolinonitrile
Figure imgf000097_0004
1H NMR (METHANOL-d4) δ 8.56-8.32 (m, 4H), 8.03-8.02 (m, IH), 7.67-7.57 (m. 3H), 4.42-4.33 (m, IH), 1.36-1.28 (br, 6H). LC-MS: m/z 332.1 (M+H)+.
Compound 199 - N2-(2-chloropyridin-4-yl)-I^ sopropyl-6^henyl-l,3,5-triazine-2,4-diamine
Figure imgf000098_0001
1H NMR (METHANOL-d4) δ 8.43-8.37 (m, 2H), 8.23-8.10 (m, 2H), 7.67-7.66 (m, IH), 7.55-7.45 (m. 3H), 4.27-4.24 (m, IH), 1.327-1.311 (d, J = 6.4 Hz, 6H). LC-MS: m/z 341.2 (M+H)+.
(2-ethoxypyridin-4-yl)-N4-isopropyl-6-phenyl-l,3,5-triazine-2,4-diamine
Figure imgf000098_0002
1H NMR (METHANOL-d4) δ 8.41-8.36 (m, 2H), 7.91-7.88 (m, IH), 7.52-7.45 (m. 4H), 7.30-7.29 (m, IH), 4.30-4.25 (m, IH), 1.42-1.38 (t, 3H), 1.308-1.292 (d, J = 6.4 Hz, 6H). LC-MS: m/z 351.2 (M+H)+.
Compound 202 - 2-isopropyl-6^henyl-N4-(2-(trifluoromethyl)pyridin-4-yl)-l,3,5-triazine-2,4^
Figure imgf000098_0003
1H NMR (METHANOL-d4) δ 10.45-10.27 (m, IH), 8.68-8.28 (m, 4H), 7.99-7.51 (m, 5H), 4.17-4.16 (m., IH), 3.25 (s, 6H), 1.24 (dd, J = 4, 400 MHz, 6H). LC-MS: m/z 375.1 (M+H)+.
(4-(isopropylamino)-6-phenyl-l,3,5-triazin-2-ylamino)nicotinonitrile
Figure imgf000098_0004
1H NMR (METHANOL-d4) δ 8.75-9.25 (m, 2H), 8.34-8.48 (m, 3H), 7.76-7.51 (m, 3H), 4.0-4.58 (m, IH), 1.30 (d, J = 6.8 Hz, 6H). LC-MS: m/z 331.9 (M+H)+.
(2-fluoropyridin-4-yl)-N4-isopropyl-6-phenyl-l,3,5-triazine-2,4-diamine
Figure imgf000099_0001
1H NMR (METHANOL-d ) δ 8.43-8.37 (m, 2H), Ί .99-1.91 (m, IH), 7.86-7.80 (m, IH), 7.65-7.45 (m. 4H), 4.28-4.22 (m, IH), 1.315-1.299 (d, J = 6.4 Hz, 6H). LC-MS: m/z 325.1 (M+H)+.
Compound 224 - 2-(2-(ethylamino)pyridin-4-yl)-I^-isopropyl-6^henyl-l,3,5-triazine-2,4-d
Figure imgf000099_0002
1H NMR (METHANOL-d4) δ 8.53-8.49 (m, IH), 8.42-8.36 (m, 2H), 7.74-7.72 (m, 2H), 7.53-7.46 (m, 3H), 7.03-.6.99 (m. IH), 4.42-4.24 (m, IH), 3.36-3.31 (m, 2H), 1.34-1.16 (m, 9H). LC-MS: m/z 350.0 (M+H)+.
Compound 266 - N2 sopropyl-6^henyl-l^-(pyrimidin-5-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000099_0003
1H NMR (METHANOL-d4) δ 9.25 - 9.30 (m, 2H), 8.78 - 8.79 (m, IH), 8.36 - 8.43 (m,2H), 7.45 - 7.53 (m, 3H), 4.25 - 4.62 (m,lH),1.31 (d, J = 6.4 Hz, 6H). LC-MS: m/z 308.2 (M+H)+.
Compound 277 - N2-(3-(ethylsulfinyl)phenyl)-I^ sopropyl-6-phenyl-l,3,5-triazine-2,4-diamine
Figure imgf000099_0004
1H NMR (METHANOL-d4) δ 8.51-8.32 (m, 3H), 7.76-7.52 (m, 4H), 7.35-7.27 (m, IH), 4.50-4.32 (m, IH), 3.14-3.03 (m, IH), 2.94-2.89 (m, IH), 1.33 (d, J=6.0 Hz, 6H), 1.23 (t, J=7.2 Hz, 3H). LC-MS: m/z 382.1 (M+H) +.
Compound 281 - N2-isopropyl-N4-( 6-methylpyridin-3-yl)-6-phenyl-l,3,5-triazine-2,4-diamine
Figure imgf000100_0001
1H NMR (METHANOL-d ) δ 8.99-8.83 (m, IH), 8.40-8.35 (m, 2H),8.32-8.13 (m, IH), 7.55-7.45 (m, 3H), 7.30-7.28 (m, 1Η),4.46-4.22 (m, IH), 2.52 (s, 3H), 1.30 (d, J=6.8 Hz, 6H). LC-MS: m/z 321.2 (M+H) +.
Compound 289 - N2-( 6-chloropyridin-3-yl)-I^-isopropyl-6-phenyl-l,3,5-triazine-2,4-diamine
Figure imgf000100_0002
1H NMR (METHANOL-d ) δ 8.79-8.86 (m, 1Η), 8.25-8.40 (m, 3Η), 7.37-7.53 (m,4H), 4.40-4.61 (m, IH), 1.30 (d, J = 6.4 Hz, 6H). LC-MS: m/z 340.9 (M+H) +.
Compound 293 - 2-(2-(dimethy^mino)pyridin-4-yl)-N4 sopropyl-6-phenyl-l,3,5-tr z
Figure imgf000100_0003
1H NMR (METHANOL-d4) δ 8.44-8.38 (m, 2H), 7.86-7.79 (m, 2H), 7.54-7.45 (m, 3H), 7.02-7.00 (m, IH), 4.30 (m., IH), 3.25 (s, 6H), 1.30 (dd, J = 8, 400 MHz, 6H). LC-MS: m/z 350.1 (M+H)+. Compound 301 -
N2 sopropyl-I^-(2-(isopropylamino)pyridin-4-yl)-6^henyl-l,3,5-triazine-2,4-d
Figure imgf000101_0001
H NMR (DMSO-d4) δ 1.03-1.09 (m, 12H), 3.57-3.74 (m 1H), 3.99-4.18 (m, 1H), 7.00 (br, 7.34-8.35 (m, 9H), 10.7 (d, 1H). LC-MS: m/z 364 (M+H)+.
Compound 302 - 2-isopropyl-I^-(2-(methylamino)pyridin-4-yl)-6-phenyl-l,3,5-triazine-2,4-d
Figure imgf000101_0002
1H NMR (METHANOL-d ) δ 8.42-8.35 (m, 2H), 7.79-7.54 (m, 5H), 7.12-7.10 (m, 1H), 4.35 (m., 1H), 3.03 (s, 3H), 1.30 (dd, J = 16, 400 MHz, 6H). LC-MS: m/z 336.2 (M+H)+.
Compound 303 - 2-isopropyl-N4-( 6-( methylamino )pyridin-3-yl)-6-phenyl-l,3,5-triazine-2,4-diamine
Figure imgf000101_0003
1H NMR (METHANOL-d4) δ 8.50 (m, 1H), 8.25-8.24 (m, 2H), 8.07-8.05 (m, 1H), 7.75-7.63 (m, 3H), 7.14-7.11 (m, 1H), 4.35 (m., 1H), 3.07 (s, 3H), 1.35 (dd, J = 8, 400 MHz, 6H). LC-MS: m/z 336.2 (M+H)+.
Compound 308 - 2 sopropyl-I^-(l-methyl-lH^yrazol-4-yl)-6^henyl-l,3,5-triazine-2,4-diamine
1H NMR (METHANOL-d ) δ 8.49-8.20 (m, 2H), 8.21-8.15 (m, 1Η),7.70-7.50 (m, 4H), 4.49-4.25 (m, 1H), 3.91 (s, 3H), 1.33 (d, J=6.8 Hz, 6H). LC-MS: m/z 310.2 (M+H). sopropyl-N4-(isoxazol-4-yl)-6-phenyl-l,3,5-tr zine-2,4-diamine
Figure imgf000102_0001
1H NMR (METHANOL-d4) δ 9.30-9.12 (m, 1H), 8.57 (s, 1H), 8.39-8.34 (m, 2H), 7.53-7.47 (m,
3H), 4.41-4.25 (m, 1H), 1.31 (d, J = 5.2 Hz, 6H). LC-MS: m/z 297.2 (M+H).
Compound 310 - N2-(2,6-dimethylpyridin-4-yl)-N4 sopropyl-6^henyl-l,3,5-triazine-2,4-diamine
Figure imgf000102_0002
1H NMR (METHANOL-d4) δ 8.46-8.40 (m, 2H), 8.08-8.06 (m, 2H), 7.57-7.48 (m, 3H),4.47-4.20 (m, 1H), 2.66 (s, 6H), 1.34 (d, J = 6.4 Hz, 6H). LC-MS: m/z 335.3 (M+H) +.
Compound 311 - 2-(6-(cyclopropylmethoxy)pyridin-3-yl)-N4 sopropyl-6-phenyl-l,3,5-tr zine-2,4-d
Figure imgf000102_0003
1H NMR (METHANOL-d4) δ 8.56-8.34 (m, 3H), 8.09-8.07 (m, 1H), 7.53-7.45 (m, 3H), 6.84-6.81 (m, 1H), 4.41-4.25 (m, 1H), 4.10 (d, J = 6.8 Hz, 1H), 1.30 (d, J = 6.4 Hz, 1H), 1.21-1.20(m, 1H), 0.65-0.61(m, 2H), 0.39-0.36(m, 2H). LC-MS: m/z 377.3 (M+H) +.
Compound 312 - 2-(6 sopropoxypyridin-3-yl)-N4 sopropyl-6-phenyl-l,3,5-tr zine-2,4-d mine
Figure imgf000102_0004
1H NMR (METHANOL-d4) δ 8.59-8.42 (m, 3H), 8.07-8.04 (m, IH), 7.53-7.45 (m, 3H), 6.77-6.75 (m, IH), 5.19-5.16 (m, IH), 4.43-4.21 (m, IH), 1.35 (d, J = 6.0 Hz, 6H), 1.29 (d, J = 6.4 Hz, 6H). LC-MS: m/z 365.2 (M+H) +.
Compound 313 - N2 sopropyl-6^henyl-N4-(th zol-5-yl)-l,3,5-tr zine-2,4-d mine
Figure imgf000103_0001
1H NMR (METHANOL-d ) δ 8.59-8.38 (m, 3H), 7.69-7.48 (m, 4H), 4.45-4.23 (m, IH), 1.22 (d, J = 6.8 Hz, 6H). LC-MS: m/z 313.1 (M+H) +.
Compound 314 - 2-isopropyl-6^henyl-N4-(3-(trifluoromethyl)pyridin-4-yl)-l,3,5-triazine-2,4-d
Figure imgf000103_0002
1H NMR (METHANOL-d4) δ 9.58 (s, IH), 9.35 (s, IH), 8.45-8.40 (m, 2H), 7.56-7.42 (m, 3H), 7.11 (s, IH), 4.28-4.25 (m, IH), 1.25 (d, J = 6.4 Hz, 6H). LC-MS: m/z 375.2 (M+H) +.
Compound 315 - 2-(2-cyclopropylpyridin-4-yl)-N4 sopropyl-6-phenyl-l,3,5-triazine-2,4-diamine
Figure imgf000103_0003
1H NMR (METHANOL-d ) δ 8.43-8.34 (m, 2H), 8.21-8.18 (m, IH), 7.93-7.16 (m, 2H), 7.54-7.45 (m. 3H), 4.29-4.26 (m, IH), 2.15-2.12 (m, IH), 1.319-1.303 (d, J = 6.4 Hz, 6H), 1.19-1.18 (m, 2H) 1.03-1.02 (m, 2H). LC-MS: m/z 347.3 (M+H)+.
Compound 316 -
N2-(6-cyclopropylpyridin-3-yl)-N4 sopropyl-6-phenyl-l,3,5-triazine-2,4-diamine
Figure imgf000104_0001
1H NMR (METHANOL-d4) δ 9.01-8.98 (m, IH), 8.40-8.34 (m, 2H), 8.16-8.13 (m, IH),
7.54-7.44 (m, 3H), 7.27-7.25 (m. IH), 4.27-4.24 (m, IH), 1.299-1.282 (d, J = 6.8 Hz, 6H), 1.11-1.06 (m, 2H) 0.97-0.96 (m, 2H). LC-MS: m/z 347.3 (M+H)+.
Compound 329 -
N2-isopropyl-6^henyl-N4-(5-(trifluoromethyl)pyridin-3-yl)-l,3,5-triazine-2,4-d
Figure imgf000104_0002
1H NMR (METHANOL-d4) δ 8.99-9.03 (m, 2H), 8.36-8.47 (m, 3H), 7.45-7.52 (m,3H), 4.18-4.57 (m, IH), 1.30 (d, J = 6.4 Hz, 6H). LC-MS: m/z 375.2 (M+H)+.
Compound 332 - 2-isopropyl-I^-(l-methyl-lH midazol-4-yl)-6-phenyl-l,3,5-triazine-2,4-diamine
Figure imgf000104_0003
1H NMR (METHANOL-d ) δ 8.51-8.22 (m, 3H), 7.48-7.38 (m, 3H), 7.28 (s, IH), 4.38-4.12 (m,
IH), 3.83 (s, 3H), 1.18 (d, J = 6.4 Hz, 6H). LC-MS: m/z 309.9 (M+H).
Compound 129 - N2 sopropyl-6-p enyl-l^-(pyruiin-4-yl) ,3,5-tr zine-2,4-d mine
Figure imgf000104_0004
1H NMR (METHANOL-d4) d 14.92 (br. s., IH), 112.-11.13 (m, IH), 8.68-8.63 (m, 2H), 8.41-8.36 (m, 4H), 8.24-8.10 (m, IH), 7.63-7.53 (m, 3H), 4.34-4.17 (m., IH), 1.17 (dd, J = 4, 400 MHz, 6H). LC-MS: m/z 307.2 (M+H)+.
Figure imgf000105_0001
1H NMR (METHANOL-d4) 9.17-9.11 (m, 2H), 8.42-8.35 (m, 2H), 7.55-7.44 (m. 3H), 4.26-4.23 (m, IH), 2.66 (s, 3H), 1.308-1.292 (d, J = 6.4 Hz, 6H). LC-MS: m/z 322.2 (M+H)+.
Compound 376 - 2-(3-(azetidin-l-ylsulfonyl)phenyl)-N4 sopropyl-6^henyl-l,3,54r zine
Figure imgf000105_0002
1H NMR (METHANOL-d4) 8.99-8.86 (m, IH), 8.44-8.38 (m, 2H), 7.77-7.75 (m, IH), 7.60-7.44 (m. 5H), 4.35-4.32 (m, IH), 3.82-3.78 (m, 4H), 2.10-2.02 (m, 2H), 1.300-1.284 (d, J = 6.4 Hz, 6H). LC-MS: m/z 425.2 (M+H)+.
Example 2. Preparation of Compounds of Formula I Wherein Ring A is Optionally Substituted Pyridin-2-yl or Pyrimnidin-2-yl. The compounds of this Example are prepared by general Scheme 2, set forth below.
Scheme 2
Figure imgf000106_0001
Formula I
Example 2, step 1: Preparation of l-phenyl-2-cyanoguanidine (5). To a solution of NaN(CN)2 (50 g, 0.5618 mol) in water (430 mL) at 80°C was added a solution of aniline (26.2 g, 0.28 mol) in water and cone. HCI (132 mL/23.5 mL). The mixture was heated to 90°C for 16 hours. The mixture was cooled to room temperature and quenched by adding saturated sodium bicarbonate (317 mL). The mixture was filtered and the filter cake was dried via vacuum to afford
l-phenyl-2-cyanoguanidine as a white solid.
Figure imgf000106_0002
1H NMR (DMSO-d4) δ 6.95 (s, 2H), 7.02-7.06 (m, 1 H), 7.26-7.32 (m, 4 H), 9.00 (s, 1H).
The procedure set forth in Example 2, step 1 was used to produce the following intermediates (5) using the appropriate starting material 4.
l-(3-cyanophenyl-2-cyanoguanidine as a brown solid.
N
I I
a NH
NAN'CN
H H . LC-MS: m/z 185.9 (M+H)+.
l-methanesulfonyl-benzenyl-2-cyanoguanidine as a pale gray solid.
Figure imgf000107_0001
. LC-MS: m/z 238.8 (M+H)+.
l-3-fluoro-pyridin-2-cyanoguanidine as a pale solid.
Figure imgf000107_0002
1H NMR (DMSO-d4) δ 7.42 (s, 2H), 7.85-8.01 (m, 1 H), 8.24 (s, 1 H), 8.38 (s, 1H).
-3-chloro-pyridin-2-cyanoguanidine as a pale gray solid.
Figure imgf000107_0003
1H NMR (DMSO-d4) δ 8.06 (s, 1H), 8.29 (s, 1 H), 8.47 (s, 1H).
l-2-fluoro-pyridin-2-cyanoguanidine as a brown solid.
Figure imgf000107_0004
1H NMR (DMSO-d4) δ 7.10-7.20 (m, 1H), 7.95-7.99 (m, 1 H), 8.15 (s, 1H).
l-3,5-difluoro-phenyl-2-cyano-guanidine as white solid, which was directly used in the next step without further purification.
Figure imgf000107_0005
Example 2, step 2: Preparation of l-phenyl-2-isopropylamine-diguanidine(7) . To a mixture of l-phenyl-2-cyanoguanidine (5.0 g, 0.031 mol) in ethanol/water (46mL/18.4 mL) was added CuS04.5H20 (3.91 g, 0.01563 mol), followed by isopropyl amine (5.53 g, .03975 mol). The mixture was heated to reflux for 16 hours. To the mixture was added water (137 mL) and aq.HCl (15.5 mL in 93 mL of water) at 25-30°C. The resultant mixture was stirred at r.t. for 30 min. Then Na2S (12.4 g in 62 mL of water) was added and stirred for another 30 min. The insoluble CuS was filtered off. The filtrate was cooled to 10°C and added aqueous NaOH (7 g NaOH in 50 mL water) dropwise. The mixture was extracted with dichloromethane (100 mLx3). The organic layer was combined, dried over Na2S04 and concentrated to give l-phenyl-2-isopropylamine-diguanidine as a brown solid.
Figure imgf000108_0001
1H NMR (DMSO-d4) δ 1.25 (d, J = 4.8 Hz, 6 H), 4.91-4.97 (m, 1H), 7.17-7.39 (m, 5H).
The procedure set forth in Example 2, step 2 was used to produce the following intermediates (7) using the appropriate intermediate 5 and the appropriate amine 6.
l-3-cyanophenyl-2-isopropylamine-diguanidine as a brown solid.
Figure imgf000108_0002
. LC-MS: m/z 245 (M+H)+.
1-m thanesulfonyl -2-isopropyl-diguanidine as a pale
Figure imgf000108_0003
. LC-MS: m/z 298 (M+H)+.
l-3-fluoro-pyridin-2-cyclobutyl-diguanidine as a red solid.
Figure imgf000108_0004
l-3-chloro-pyridin-2-cyclobutyl-diguanidine as a red solid.
Figure imgf000108_0005
. LC-MS: m/z 267 (M+H)+.
l-2-fluoro-pyridin-2-cyclobutyl-diguanidine as a red solid.
Figure imgf000109_0001
. LC-MS: m/z 250.8 (M+H)+.
l-3,5-difluoropneyl-2-isopropyl-diguanidine as a brown solid, which was used in the next step without further purification.
Figure imgf000109_0002
Example 2, step 3: Preparation of Compound 214 -
N-Isopropyl-N'-phenyl-6-pyridin-2-yl-[l,3,5]triazine-2,4-diamine. To a mixture of
N-isopropyl-N'-phenyl-6-pyridin-2-yl-[l,3,5]triazine-2,4-diamine (0.5 g, 2.28 mmol) and pyridine-2-carboxylic acid methyl ester (0.312 g, 2.28 mmol) in methanol (7 mL) was added NaOMe (0.25 g, 4.56 mmol). The mixture was stirred at r.t. for 16 hours. The mixture was poured into water and extracted with ethyl acetate (50 mL), dried over Na2S04, concentrated and purified by a standard method to afford N-isopropyl-N'-phenyl-6-pyridin-2-yl-[l,3,5]triazine-2,4-diamine.
Figure imgf000109_0003
1H NMR (METHANOL-d4) δ 8.72-8.73 (d, IH), 8.47-8.49 (d, IH), 7.97-8.01 (t, IH), 7.77-7.79 (d, 2H),7.56-7.59 (t, IH), 7.31-7.35 (t, 2H), 7.04-7.07 (t, IH), 4.40-4.45 (m, IH), 1.30-1.31 (d, 6H). LC-MS: m/z 307.0 (M+H)+.
Additional compounds of Formula I set forth below were similarly produced following Scheme 2 utilizing the appropriate intermediates and reagents.
Compound 228 - 6-(4-chloropyridin-2-yl)-N2 sopropyl-I^-phenyl-l,3,5-triazine-2,4-diamine
Figure imgf000109_0004
1H NMR (METHANOL-d4) δ 8.63-8.64 (d, IH), 8.48 (s, IH), 7.73-7.75 (d, 2H), 7.63 (s, IH), 7.29-7.31 (t, 2H), 7.05-7.10 (t, IH), 4.21-4.24 (m, IH), 1.27-1.29 (d, 6H). LC-MS: m/z 341.0 (M+H)+.
Compound 229 - 6-( 6-chloropyridin-2-yl)-N2 sopropyl-I^-phenyl-l,3,5-triazine-2,4-diamine
Figure imgf000110_0001
1H NMR (METHANOL-d ) δ 8.37-8.39 (d, IH), 7.91-7.95 (t, IH), 7.72-7.74 (d, 2H), 7.56-7.58 (d, IH), 7.29-7.32 (t, 2H), 7.02-7.04 (t, IH), 4.23-4.29 (m, IH), 1.27-1.28 (d, 6H). LC-MS: m/z 341.0 (M+H)+.
Compound 230 - 6-(3-chloropyridin-2-yl)-N2 sopropyl-I^-phenyl-l,3,5-triazine-2,4-diamine
Figure imgf000110_0002
1H NMR (METHANOL-d4) δ 8.54-8.55 (d, IH), 8.01-8.03 (d, IH), 7.70-7.72 (d, IH), 7.50-7.53 (m, IH), 7.27-7.31 (t, 2H), 7.04 (s, IH), 4.32-4.40 (m, IH), 1.21-1.30 (m, 6H). LC-MS: m/z 340.9 (M+H)+.
Compound 231 - 6-(4-(isopropylamino)-6-(phenylamino)-l,3,5-triazin-2-yl)pyridin-2-ol
Figure imgf000110_0003
1H NMR (METHANOL-d ) δ 7.70-7.75 (m, 3H), 7.43-7.47 (d, IH), 7.28-7.33 (t, 2H), 7.02-7.07 (t, IH), 6.68-6.72 (m, IH), 4.28-4.39 (m, IH), 1.33-1.35 (d, 6H). LC-MS: m/z 323.0 (M+H)+.
opropylamino)-6-(pyridin-2-yl)-l,3,5-triazin-2-ylamino)benzonitrile
Figure imgf000110_0004
1H NMR (METHANOL-d4) δ 8.71-8.72 (d, IH), 8.41-8.51 (m, 2H), 7.90-8.00 (m, 2H), 7.44-7.58 (m, 2H), 7.33-7.37 (t, IH), 4.22-4.27 (m, IH), 1.27-1.33 (m, 6H). LC-MS: m/z 332.0 (M+H)+. Compound 247 - 2-isopropyl-l^-phenyl-6-(6-(trifluoromethyl)pyridin-2-yl)-l,3,5-triazm^
Figure imgf000111_0001
1H NMR (DMSO-d6) δ 8.64-8.66 (m, IH), 8.19 (m, IH), 7.94 (m, IH), 7.77 (m, 2H), 7.27-7.34 (m, 2H), 7.05 (m, IH), 4.24-4.49 (m, IH), 1.30 (d, 6H). LC-MS: m/z 375.0 (M+H)+.
Compound 270 - 2-isopropyl-I^-phenyl-6-(4-(trifluoromethyl)pyridin-2-yl)-l,3,5-triazin^
Figure imgf000111_0002
1H NMR (METHANOL-d4) δ 8.99 (d, IH), 8.76 (m, IH), 7.89 (m, IH), 7.79 (m, 2H), 7.29-7.39 (m, 2H), 7.05 (m, IH), 4.21-4.52 (m, IH), 1.29-1.33 (m, 6H). LC-MS: m/z 375 (M+H)+.
Compound 290 - 6-( 6-aminopyridin-2-yl)-N2-isopropyl-N4-phenyl-l,3,5-triazine-2,4-diamine
Figure imgf000111_0003
1H NMR (METHANOL-d4) δ 7.92-8.03 (m, IH), 7.72-7.83 (m, IH), 7.69 (m, 2H), 7.29-7.33 (m, 2H), 7.14 (m., IH), 7.06 (m, IH), 4.15-4.51 (m, IH), 1.25 (d, 6H). LC-MS: m/z 322.1 (M+H)+. Compound 322 - 2-cyclobutyl-I^-(5-fluoropyridin-3-yl)-6-(pyridin-2-yl)-l,3,5-triazine-2,4-di^
Figure imgf000111_0004
1H NMR (DMSO-d6) δ 10.3 (s, IH), 8.69-8.85 (m, 2H), 8.34-8.59 (m, 2H), 8.17-8.29 (m, 2H), 7.99 (m, IH), 7.55 (m, IH), 4.35-4.70 (m, IH), 2.31 (m, 2H), 2.05 (m, 2H), 1.72 (m, 2H). LC-MS: m/z 337.9 (M+H)+.
Compound 323 - -(6-chloropyridin-2-yl)-N2-cyclobutyl-N4-(5-fluoropyridin-3-yl)-l,3,5
Figure imgf000112_0001
1H NMR (DMSO-d6) δ 10.4 (s, IH), 8.80 (s, IH), 8.52-8.62 (m, IH), 8.27-8.42 (m, 2H), 8.22 (m, IH), 8.09 (m, IH), 7.70 (m, IH), 4.35-4.69 (m, IH), 2.31 (m, 2H), 2.09 (m, 2H), 1.72 (m, 2H). LC-MS: m/z 372.2 (M+H)+.
Compound 325 - -(6-chloropyridin-2-yl)-N2-cyclobutyl-N4-(6-fluoropyridin-3-yl)-l,3,5-triazm^
Figure imgf000112_0002
1H NMR (DMSO-d6) δ 10.22 (s, IH), 8.59-8.69 (d, IH), 8.12-8.51 (m, 3H), 8.07 (m, IH), 7.69 (m., IH), 7.11-7.24 (m, IH), 4.32-4.66 (m, IH), 2.33 (m, 2H), 2.06 (m, 2H), 1.72 (m, 2H).
LC-MS: m/z 371.9 (M+H)+.
Compound 330 - N2-(5-chloropyridin-3-yl)-I^-cyclobutyl-6-(pyridin-2-yl)-l,3,5-triazine-2^ diamine
Figure imgf000112_0003
1H NMR (DMSO-d6) δ 10.33 (s, IH), 8.83-9.98 (m, IH), 8.76 (m, IH), 8.55-8.69 (m, IH), 8.31-8.52 (m., IH), 8.18-8.29 (m, 2H), 8.01 (m, IH), 7.57 (m, IH), 4.35-4.69 (m, IH), 2.33 (m, 2H), 2.06 (m, 2H), 1.72 (m, 2H). LC-MS: m/z 354.2 (M+H)+.
I l l Compound 331 - 2-isopropyl-6-( 6-( methylamino )pyridin-2-yl)-N4-phenyl-l,3,5-triazine-2,4-diamine
Figure imgf000113_0001
1H NMR (METHANOL-d4) δ 7.76 (m, 2H), 7.60 (m, 2H), 7.31 (m, 2H), 7.04 (m, 1H),6.64 (m, IH), 4.19-4.48 (m, IH), 2.96 (s, 3H), 1.27 (m, 6H). LC-MS: m/z 336.2 (M+H)+.
Compound 344 - -(6-chloropyridin-2-yl)-N2-(6^uoropyridin-3-yl)-N4 sopropyl-l,3,5-tr zine
Figure imgf000113_0002
1H NMR (DMSO-d6) δ 10.21-10.81 (d, IH), 8.61-8.79 (d, IH), 8.04-8.51 (m, 4H), 7.69-7.81 (m, IH), 7.12-7.24 (m, IH), 4.05-4.32 (m, IH), 1.22 (d, 6H). LC-MS: m/z 359.9 (M+H)+. 381.9 (M+Na)+.
Compound 326 - -(6-chloropyridin-2-yl)-N2 sopropyl-N4-(3-(methylsulfonyl)phenyl)-l,3,5-tr z
Figure imgf000113_0003
1H NMR (METHANOL-d ) δ 8.99 (s, IH), 8.46-8.47 (d, IH), Ί .96-1.99 (m, IH), 7.74-7.77 (m, IH), 7.55-7.62 (m, 3H), 4.32-4.50 (m, IH), 3.18 (s, 3H), 1.28-1.32 (d, 6H). LC-MS: m/z 418.9 (M+H)+.
Compound 340 -
6-(6-chloropyridin-2-yl)-N2-(3,5-difluorophenyl)-N4 sopropyl-l,3,5-triazine-2,4-di^
Figure imgf000114_0001
1H NMR (METHANOL-d4) δ 8.41-8.45 (t, IH), 8.00-8.04 (t, IH), 7.63-7.69 (m, IH), 6.64-6.69 (t, IH), 4.22-4.27 (m, IH), 1.29-1.35 (d, 6H). LC-MS: m/z 377.2 (M+H)+.
Compound 358 -
N2-isopropyl-l^-(3-(methylsulfonyl)phenyl)-6-(6-(trifluoromethy
-diamine
Figure imgf000114_0002
1H NMR (METHANOL-d4) δ 8.99 (s, IH), 8.60-8.72 (m, IH), 8.19 (t, IH), 7.81 (d, 1Η),7.77-7.78 (m, IH), 7.55-7.62 (m, 2H), 4.35 -4.47 (m, IH), 3.11-3.18 (m, 3H), 1.33 (d, 6H). LC-MS: m/z 453.2 (M+H)+.
Compound 359 -
N2-hopropyl-6-{6-methylpyridin-2-yl)-N4-{3-{methylmlfonyl)phenyl)-l
Figure imgf000114_0003
1H NMR (METHANOL-d ) δ 8.60-9.03 (m, IH), 8.31 (m, IH), 7.70-8.05 (m, 2H), 7.81 (d, IH), 7.57-7.63 (m, 2H), 7.45-7.47 (m, IH), 4.39 (m, IH), 3.12-3.19 (m, 3H), 2.67 (s, 3H), 1.34 (d, 6H). LC-MS: m/z 399.2 (M+H)+.
Compound 360 - -(6-ethynylpyridin-2-yl)-N2 sopropyl-N4-(3-(methylsulfonyl)phenyl)-l,3,5-tr z
1H NMR (METHANOL-d4) δ 8.89 (s, IH), 8.56 (d, IH), 8.15-8.19 (m, IH), 7.71-7.95 (m, 4H), 4.45 (br., IH), 4.03 (s, IH), 3.18 (s, 3H), 1.39 (d, 6H). LC-MS: m/z 409.2 (M+H)+.
Compound 361 -
N2-isopropyl-6-(6-methoxypyridin-2-yl)-N4-(3-(methylsulfonyl)pheny
Figure imgf000115_0001
1H NMR (METHANOL-d4) δ 8.55-8.99 (m, IH), 7.82-8.13 (m, 3H), 7.57-7.64 (m, 2H), 6.98 (d, IH), 4.37-4.41 (m., IH), 4.07 (s, 3H), 3.16 (s, 3H), 1.34 (d, 6H). LC-MS: m/z 414.9 (M+H)\, 436.9 (M+Na)+.
Compound 363 - 2-(6-fluoropyridin-3-yl)-I^-neopentyl-6-(pyridin-2-yl)-l,3,5-triazine-2,4-d
Figure imgf000115_0002
1H NMR (METHANOL-d ) δ 8.82 (d, IH), 8.47-8.54 (m, IH), 8.40 (d, IH), 8.14-8.17 (m, IH), 7.83-7.88 (m., IH), 7.45-7.52 (m, IH), 7.10-7.20 (m, IH), 6.93-6.99 (m, IH), 5.40-5.77 (m, IH), 3.31-3.49 (m, 2H), 1.00 (s, 9H). LC-MS: m/z 354.2 (M+H)+.
Compound 364 -
N2-isopropyl-6-(6-(methylamino)pyridin-2-yl)-N4-(3-(methylsulfonyl)phenyl)-l,3,5
lamine
Figure imgf000115_0003
1H NMR (CDC13) δ 10.00-10.31 (br., IH), 8.61-8.82 (m, IH), 7.53-8.82 (m, 5H), 6.95- 1H), 4.34 (m., IH), 3.07 (d, 6H), 1.31-1.37 (m, 6H). LC-MS: m/z 414.2 (M+H)+. Compound 365 -
N24sopropyl-N4-(3-(methylsulfonyl)phenyl)-6-(6-(prop-l-ynyl)pyridin-2-yl)- amine
Figure imgf000116_0001
1H NMR (Methanol-d4) δ 8.89 (s, IH), 8.49 (d, IH), 8.11 (t, IH), 7.80-7.86 (m, 3H), 7.71-7.75 (m., IH), 4.45 (m, IH), 3.19 (s, 3 H), 2.17 (d, 3H), 1.40 (d, 6 H). LC-MS: m/z 423.0 (M+H)+. Compound 366 -
6-(6-(difluoromethyl)pyridin-2-yl)-N24sopropyl-rf-(3-(methylsulfonyl)pfa
-diamine
Figure imgf000116_0002
1H NMR (Methanol-d4) 5 8.88 (s, IH), 8.78 (m, IH), 8.35 (s, IH), 8.10 (m, IH), 7.82 (t, 2H), 7.71 (t, IH), 6.70-7.10 (m., IH), 4.30-4.50 (m, IH), 3.17 (s, 3 H), 1.39 (d, 6 H). LC-MS: m/z 434.9 (M+H)+.
Compound 395 -
6-(6-(l,l-difluoroethyl)pyridin-2-yl)-N24sopropyl-N4-(3-(methylsulfonyl)pn^
,4-diamine
Figure imgf000116_0003
1H NMR (Methanol-d4) 5 8.98 (s, IH), 8.57 (d, IH), 8.09 (t, IH), 7.85 (d, IH), 7.80 (m, IH), 7.55-7.62 (m, IH), 4.36-4.39 (m, IH), 3.14-3.17 (m, 3H), 2.11 (t, 3H), 1.32 (d, 6H). LC-MS: m/z 449.3 (M+H)+. 471.3 (M+Na)+. Compound 397 -
6-(6-cyclopropylpyridin-2-yl)-N2 sopropyl-N4-(3-(methylsulfonyl)phenyl)-l,3,5
mine
Figure imgf000117_0001
1H NMR (METHANOL-d4) δ 8.97 (s, IH), 8.21-8.2 (d, IH), 7.76-7.80 (t, 2H), 7.55-7.61 (m, 2H), 7.25-7.27 (d, IH), 4.35-4.38 (m, IH), 3.13 (s, 3H), 2.23-2.28 (m, IH), 1.31-1.32 (d, 6H), 1.02-1.12 (m, 4H). LC-MS: m/z 425.3 (M+H)+.
Compound 398 - -(6-aminopyridin-2-yl)-N2-(3,5-difluorophenyl)-N4 sopropyl-l,3,5-triazine-2,4-d
Figure imgf000117_0002
1H NMR (METHANOL-d4) δ 7.66-7.70 (t, IH), 7.56-7.60 (t, IH), 7.49-7.51 (d, 2H), 6.70-6.73 (d, IH), 6.53-6.57 (t, IH), 4.21-4.24 (m, IH), 1.18-1.31 (m, 6H). LC-MS: m/z 358.3 (M+H)+.
Example 3. Preparation of Additional Compounds of Formula I Wherein Ring A is
Substituted Pyridin-2-yl. The compounds of this Example are prepared by general Scheme 3, set forth below.
Scheme 3
Figure imgf000118_0001
Example 3, step 1: Preparation of 6-chloro-pyridine-2-carboxylic acid methyl ester (10). To a solution of 6-chloro-pyridine-2-carboxylic acid (48 g, 0.31 mol) in methanol (770 ml) was added concentrated HC1 (6 ml). The mixture was stirred at 80°C for 48 hours then concentrated to remove the volatile. The crude product was diluted with ethyl acetated and washed with Sat. NaHCC"3 solution. The organic layer was dried with anhydrous Na2S04 and concentrated to give -chloro-pyridine-2-carboxylic acid methyl ester as a white solid.
Figure imgf000118_0002
LC-MS: m/z 172.0 (M+H)+.
The procedure set forth in Example 3, step 1 was used to produce the following intermediates (10) using the appropriate starting material 9.
6-trifluoromethyl-pyridine-2-carboxylic acid methyl ester.
Figure imgf000118_0003
LC-MS: m/z 206 (M+H)+. Example 3, step 2: Preparation of 6-(6-chloropyridin-2-yl)-l,3,5-triazine-2,4-dione . To a solution of Na (32 g, 0.16 mol) in ethanol (500 mL) was added methyl 6-chloropicolinate (32 g, 0.16 mol) and biuret (5.3 g, 0.052 mol). The mixture was heated to reflux for 1 hour. Then concentrated to give residue which was poured to water and added Sat.NaHC03 solution to adjust pH to 7, the precipitated solid was collected by filtration and dried to give
6-(6-chloropyridin-2-yl)-l,3,5-triazine-2,4-dione as a white solid.
Figure imgf000119_0001
The procedure set forth in Example 3, step 2 was used to produce the following intermediates (11) starting with appropriate intermediate 10.
6-(6-trifluoromethyl-pyridin-2-yl)-lH-l,3,5-triazine-2,4-dione as a pale white solid.
Figure imgf000119_0002
. LC-MS: m/z 259 (M+H)+.
-pyridin-2-yl-lH-l,3,5-triazine-2,4-dione.
Figure imgf000119_0003
1H NMR (DMSO-d4): δ 11.9-12.5 (s, 1H), 11.3-11.6 (s, 1H), 8.7-8.9 (m, 1H), 8.2-8.4 (m, 1H), 8.0-8.2 (m, 1H), 7.6-7.8 (m, 1H).
Example 3, step 3: Preparation of2,4-dichloro-6-(6-chloropyridin-2-yl)-l,3,5-triazine To a solution of 6-(pyridin-2-yl)-l,3,5-triazine-2,4(lH,3H)-dione (3.0 g, 013 mol) in POCl3 (48 mL) was added PC15 (23 g, 0.1 mol). The mixture was stirred at 100°C for 2 hours then concentrated to remove the volatile. The residue was diluted with ethyl acetated and washed with Sat.NaHC03 solution. The organic layer was dried over anhydrous Na2S04 and concentrated to give 2,4-dichloro-6-(6-chloropyridin-2-yl)-l,3,5-triazine as a brown solid.
CI
Figure imgf000120_0001
. LC-MS: m/z 260.9 (M+H)+.
The procedure set forth in Example 3, step 3 together with the appropriate starting intermediate 11 was used to produce the following intermediates (12).
2, 4-dichloro-6-(6-trifluoromethyl-pyridin-2-yl)-l,3,5-triazine as light yellow solid.
CI
Figure imgf000120_0002
. LC-MS: m/z 294.9 (M+H)+.
2,4-Dichloro-6-pyridin-2-yl-[l,3,5]triazine (1.0 g, 80%) as brown solid.
Figure imgf000120_0003
. LC-MS: m/z 227.0 (M+H)+.
Example 3, step 4: Preparation of 4-chloro-6-(6-chloropyridin-2-yl)-N-isopropyl-l, 3,
5-triazin-2-amine . To a solution of 2,4-dichloro-6-(pyridin-2-yl)-l,3,5-triazine (2.0 g, 0.0077 mol) in anhydrous THF (20 mL) was added isopropyl amine (0.45 g, 0.0077 mol). The mixture was stirred at room temperature for 1 hour. The mixture was quenched by water and extracted with ethyl acetate. The organic layer was dried over anhydrous Na2S04 and concentrated to give 4-chloro-6-(6-chloropyridin-2-yl)-N-isopropyl-l,3,5-triazin-2-amine which was used directly in the next step. CI
Figure imgf000121_0001
. LC-MS: m/z 221.1 (M+H)+.
The procedure set forth in Step 4 using the appropriate intermediate 12 and amine 6 was used to produce the following intermediates (13).
4-Chloro-6-(6-trifluoromethyl-pyridin-2-yl)-l, 3, 5 triazin-2-y]-isopropyl-amine .
Figure imgf000121_0002
. LC-MS: m/z 318.1 (M+H)+.
(4-Chloro-6-pyridin-2-yl-[l,3,5]triazin-2-yl)-isopropyl-
Figure imgf000121_0003
m/z 249.9 (M+H)+.
4-chloro-6-(6-chloropyridin-2-yl)-N-(oxetan-3-yl)-l,3,5-triazin-2-amine, which was used directly in the next step.
Figure imgf000121_0004
. LC-MS: m/z 298.2 (M+H)+.
4-Chloro-6-(6-trifluoromethyl-pyridin-2-yl)-l,3,5 triazin-2-y]-oxetan-3-yl-amine, which was used directly in the next step.
Figure imgf000122_0001
. LC-MS: m/z 332.1 (M+H)+.
4-chloro-N-( ( tetrahydrofuran-2-yl)-methyl)-6-( 6-(trifluoromethyl)pyridin-2-yl)-l,3,5-triazin-2-a mine which was used directly in the next step.
Figure imgf000122_0002
LC-MS: 360.1 (M+H)+.
[4-Chloro-6-(6-trifluoromethyl^yridin-2-yl)-[l,3,5]triazin-2-yl]-(3-ox
]hex-6-yl)-amine , which was used directly in the next step.
Figure imgf000122_0003
. LC-MS: m/z 358.1 (M+H)+.
-[ -Chloro-6-(6-trifluoromethyl^yridin-2-yl)-[l,3,5]triazin-2-yla
Figure imgf000122_0004
H . LC-MS: 348.0 (M+H)+.
Example 3, step 5: Preparation of
6-(6-Chloro-pyridin-2-yl)-N-oxetan-3-yl-N'-(2-trifluoromethyl-pyridin
-4-yl)-[l,3,5]triazine-2,4-diamine-Compound 356. To a solution of
4-chloro-6-(6-chloropyridin-2-yl)-N-(oxetan-3-yl)-l,3,5-triazin-2-amine (0.23 g, 0. 78 mmol) in anhydrous dioxane (3 mL) was added 2-trifluoromethyl-pyridin-4-ylamine (0.13 g, 0.78 mmol), t-BuONa (0.15g, 1.56 mmol) and Pd(dppf)Cl2 (0.057g, 0.078 mmol). The mixture was stirred at 80°C under N2 for 1 hour. The mixture was quenched by water and extracted with ethyl acetate. The organic layer was dried with anhydrous Na2S04, concentrated and purified by a standard method to give 6-(6-chloro-pyridin-2-yl)-N-oxetan-3-yl-N'-(2-trifluoromethyl-pyridin-4-yl)- amine.
Figure imgf000123_0001
1H NMR (METHANOL-d ) : δ 8.5 (m, 2H), 8.4 (m, IH), 8.3-8.1 (m, 0.5H), 7.96 (m, IH), 7.85 (m, 0.6H), 7.6 (m, IH), 5.1-5.5 (m, IH), 5.0 (m, 2H), 4.7(m, 2H). LC-MS: m/z 424.2 (M+H)+.
Additional compounds of Formula I set forth below were similarly produced following Scheme 3 utilizing the appropriate intermediates and reagents.
Compound 334 - 2-isopropyl-6^henyl-N4-(2-(trifluoromethyl)pyridin-4-yl)-l,3,5-trm^
Figure imgf000123_0002
1H NMR (METHANOL-d ) : δ 8.65-8.75 (m, 2H), 8.5 (m, 2H), 8.15-8.3 (m, 0.5H), 8.0 (m, IH), 7.82 (m, 0.6H), 4.2-4.6 (m, IH), 1.3 (d, J = 6.4 Hz, 6H). LC-MS: m/z 375.0 (M+H)+.
Compound 335 -
N2-isopropyl-6-( 6-( trifluoromethyl)pyridin-2-yl)-lS f-( 2-( trifluoromethyl)pyridin-4-yl)-l,3,5-triazi -2,4-diamine
Figure imgf000123_0003
1H NMR (METHANOL-d ) : δ 8.6 (m, 2H), 8.5 (m, IH), 8.1-8.2 (m, IH), 7.78 (m, 0.7H),
4.24-4.27 (m, IH), 1.3 (d, J = 6.8 Hz, 6H). LC-MS: m/z 444.3 (M+H)+. Compound 336 -
N2-(oxetan-3-yl)-6-(pyridin-2-yl)-N4-(2-(trifluoromethyl)pyridin-4-yl)-l,3,^
Figure imgf000124_0001
1H NMR (METHANOL-d4): δ 8.7 (m, IH), 8.46-8.52 (m, 3H), 7.89-8.23 (m, 2H), 7.6 (m, IH), 5.15-5.55 (m, IH), 5.0 (m, 2H), 4.7 (m, 2H). LC-MS: m/z 390.2 (M+H)+.
Compound 337 -
N2-(isoxazol-4-yl)- -(oxetan-3-yl)-6-(6-(trifluoromethyl)pyridin-2-yl)-l,3
Figure imgf000124_0002
1H NMR (METHANOL-d4): δ 9.35-9.05 (m, IH), 8.6-8.7 (m, 2H), 8.2 (m, IH), 8.0 (m, IH), 5.2-5.4 (m, IH), 5.0 (m, 2H), 4.7-4.8 (d, J = 6.4 Hz, 6H). LC-MS: m/z 343.2 (M+H)+.
Compound 345 - 2-cyclobutyl-I^-(6-fluoropyridin-3-yl)-6-(pyridin-2-yl)-l,3,5-triazine-2,4^
Figure imgf000124_0003
1H NMR (DMSO-d6) δ 10.11 (br.s., IH), 8.75-8.69 (m, 2H), 8.38-8.32 (m, 2H), 8.26-8.06 (m, IH), 7.98-7.94 (m, IH), 7.56-7.52 (m, IH), 7.19-7.11 (m, IH), 4.65-4.39 (m, IH), 2.31-2.27 (m, 2H), 2.09-2.02(m, 2H), 1.70-1.67 (m, 2H). LC-MS: m/z 338.2 (M+H)+.
Compound 363 -
N2-(6-fluoropyridin-3-yl)-I^-neopentyl-6-(pyridin-2-yl)-l,3,5-triazine-2,4-d
Figure imgf000125_0001
1H NMR (CDCI3) δ 8.82 (s., IH), 8.53-8.41 (m, IH), 8.41-8.39 (m, IH), 8.17-8.09 (m, IH), 7.88-7.83 (m, IH), 7.49-7.42 (m, IH), 7.25-7.15 (m, IH), 6.99-6.92 (m, IH), 5.76-4.90 (m, 3.48-3.31(m, 2H), 1.01 (s, 9H). LC-MS: m/z 354.2 (M+H)+.
Compound 353 - -(6-chloropyridin-2-yl)-N2 sopropyl-N4-(pyrimidin-5-yl)-l,3,5-triazine-2,4-d
Figure imgf000125_0002
1H NMR (METHANOL-d4): δ 9.37 (m, IH), 8.8 (m, IH), 8.4 (m, IH), 7.97 (m, IH), 7.6 (m, 4.2-4.5 (m, 2H), 1.3 (m, 2H). LC-MS: m/z 390.2 (M+H)+.
Compound 354 - -(6-chloropyridin-2-yl)-N2-(2-chloropyridin-4-yl)-N4 sopropyl-l,3,54^
Figure imgf000125_0003
1H NMR (METHANOL-d4): δ 8.41-8.44 (m, IH), 8.17-8.22 (m, 2H), 7.96-8.0 (m, IH), Ί .62-1.66 (m, 2H), 4.2-4.6 (m, IH), 1.35 (d, J = 6.8 Hz, 6H). LC-MS: m/z 376.2 (M+H)+.
Compound 355 - -( 4-( 6-chloropyridin-2-yl)-6-( isopropylamino )-l,3,5-triazin-2-ylamino )picolinonitrile
Figure imgf000125_0004
1H NMR (METHANOL-d ) : δ 8.55-8.7 (m, 3H), 8.0 (m, 2H), 7.65 (m, IH), 4.6-4.25 (m, IH), 1.35 (d, J = 6.4 Hz, 6H). LC-MS: m/z 367.2 (M+H)+. Compound 357 - 2-(oxetan-3-yl)-N4-(th zol-5-yl)-6-(6-(trifluoromethyl)pyridin-2-y^
Figure imgf000126_0001
1H NMR (METHANOL-d4): δ 9.19-8.79 (m, 2 H), 8.50-8.40 (m, IH), 8.25-8.19 (m, IH), 7.93-7.81 (m, IH), 5.21-5.06 (m, IH), 5.02-4.90 (m, IH), 4.44-4.38 (m, IH), 3.83-3.72 (m, 2H). LC-MS: m/z 396.1 (M+H)+.
Compound 367 - l-(4-(6-chloropyridin-2-yl)-6-(5-(trifluoromethyl)pyridin-3-ylamino)-l,3,5-tr ^
methylpropan-2-ol
Figure imgf000126_0002
1H NMR (METHANOL-d4) δ 8.98 (s, IH), 8.94 (s, IH), 8.49 (s, IH), 8.41-8.39 (m, IH), 7.98-7.94 (s, IH), 7.62-7.60 (m., IH), 3.53 (s, 2H), 1.26 (s., 6H). LC-MS: m/z 440.2 (M+H) Compound 368 - l-( 4-( 6-chloropyridin-2-yl)-6-( 2-fluoropyridin-4-ylamino )-l,3,5-triazin-2-ylamino )-2-methylprop -2-ol
Figure imgf000126_0003
1H NMR (METHANOL-d4) δ 8.37-8.33 (m, IH), 7.94-7.90 (m, 2H), 7.68 (s, IH), 7.54-7.42 (m, 2H), 3.46 (s, 2H), 1.19 (s., 6H). LC-MS: m/z 390.2 (M+H)
Compound 377 -
N2-(2-fluoropyridin-4-yl)-I^-(oxetan-3-yl)-6-(6-(trifluoromethyl)pyridin-2-yi
diamine
Figure imgf000127_0001
1H NMR (METHANOL-d4): δ 8.67 (m, IH), 8.2 (m, IH), 7.8-8.05 (m, 3H), 7.5 (m, IH), 5.15-5.4 (m, IH), 5.0 (m, 2H), 4.75(m, 2H). LC-MS: m/z 408 (M+H)+.
Compound 378 -
N2-(oxetan-3-yl)-6-(6-(trifluoromethyl)pyridin-2-yl)-N4-(2-(trifluorom
iazine-2,4-diamine
Figure imgf000127_0002
1H NMR (METHANOL-d4): δ 8.7 (m, IH), 8.6-8.35 (m, 2H), 8.1-8.3 (m, 1.4H), 7.85-8.0 (m, 1.7H), 5.4-5.15 (m, IH), 5.02 (m, 2H), 4.75(m, 2H). LC-MS: m/z 458.2 (M+H)+.
Compound 379 -
N2-(oxetan-3-yl)-6-(6-(trifluoromethyl)pyridin-2-yl)-N4-(5-(trifluorometh^
iazine-2,4-diamine
Figure imgf000127_0003
1H NMR (DMSO-d6): δ 10.2-10.8 (m, IH), 9.0-9.4 (m, 2H), 8.5-8.9 (m, 3H), 8.3 (m, IH), 8.1 (m, IH), 5.0-5.2 (m, IH), 4.7(m, 2H), 4.6(m, 2H). LC-MS: m/z 458.2 (M+H)+.
Compound 380 -
N2-( 6-fluoropyridin-3-yl)-lS f-( oxetan-3-yl)-6-( 6-( trifluoromethyl)pyridin-2-yl)-l,3,5-triazine-2,4- diamine 1H NMR (METHANOL-d4): δ 8.5-8.7 (m, 2H), 8.3-8.55 (m, 2H), 8.2 (m, IH), 7.97 (m, IH), 7.0-7.15 (m, IH), 5.1-5.4 (m, IH), 5.0(m, 2H), 4.7(m, 2H). LC-MS: m/z 407 (M+H)+.
Compound 381 -
N2-(5-fluoropyridin-3-yl)-I^-(oxetan-3-yl)-6-(6-(trifluoromethyl)pyridin-2-yi
diamine
Figure imgf000128_0001
1H NMR (METHANOL-d4): δ 8.6-8.7 (m, 3H), 8.1-8.22 (m, 2H), 7.95 (m, IH), 5.1-5.4 (m, IH), 5.0 (m, 2H), 4.72 (m, 2H). LC-MS: m/z 407 (M+H)+.
Compound 382 -
5-( 4-( 6-chloropyridin-2-yl)-6-( isopropylamino )-l,3,5-triazin-2-ylamino )nicotinonitrile
Figure imgf000128_0002
1H NMR (METHANOL-d4) δ 9.12 (s, IH), 8.95-8.77 (m, 2H), 8.71-8.67 (m, IH), 8.56-8.51 (m, IH), 8.19-8.15 (m, IH), 7.88-7.86 (m, IH), 4.60-4.29 (m, IH), 1.40 (d, J = 6.4 Hz, 6H) LC-MS: m/z 367.2 (M+H)+.
Compound 383 -
6-(6-chloropyridin-2-yl)-N2-(5-fluoropyridin-3-yl)-N4 sopropyl-l,3,5-triazine-2,4-di^
Figure imgf000128_0003
1H NMR (METHANOL-d4) δ 8.88 (s, IH), 8.52 -8.49 (m, 2H), 8.32-8.30 (m, IH), 8.20-8.16 (m, IH), 7.89-7.87 (m, IH), 4.35-4.31 (m, IH), 1.40 (d, J = 6.4 Hz, 6H). LC-MS: m/z 360.1 (M+H)+. Compound 384 -
6-(6-chloropyridin-2-yl)-N2-(2-fluoropyridin-4-yl)-N4 sopropyl-l,3,5-triazine-2,4^
Figure imgf000129_0001
1H NMR (METHANOL-d4) δ 8.45-8.41 (m, IH), 8.02-7.96 (m, 2H), 7.79 (s, IH), 7.63-7.61 (m, IH), 7.54-7.49 (m, IH), 4.47-4.24 (m, IH), 1.32 (d, J = 6.4 Hz, 6H). LC-MS: m/z 360.1 (M+H)+. Compound 385 - l-(4-(6-fluoropyridin-3-ylamino)-6-(6-(trifluoromethyl)pyridin-2-yl)-l,3,5-tri
methylpropan-2-ol
Figure imgf000129_0002
1H NMR (METHANOL-d4) δ 8.63-8.75 (m, 2 H), 8.42-8.56 (m, 1 H), 8.26-8.30 (q, J = 8, 1 H), 8.04-8.06 (d, J = 7.2 Hz, 1 H), 7.16-7.19 (m, 1 H), 3.60-3.68 (d, J = 32.4 Hz, 2 H), 1.35 (s., 6 H). LC-MS: m/z 424.2 (M+H)+.
Compound 386 -
N2 -isopropyl-6-( 6-( trifluoromethyl)pyridin-2-yl)-lS f-( 5-( trifluoromethyl)pyridin-3-yl)-l,3,5-triazi -2,4-diamine
Figure imgf000129_0003
1H NMR (METHANOL-d ) δ 9.04-8.96 (m, 2 H), 8.68-8.64 (m, 1 H), 8.49-8.47 (m,l H), 8.20-8.16 (m ,1 H), 7.96-7.94 (d, J = 8.0 Hz, 1 H),4.60-4.20 (m, 1 H), 1.31 (d, J = 6.4 Hz, 6 H). LC-MS: m/z 444.2 (M+H)+.
Compound 388 - l-( 4-( 6-chloropyridin-2-yl)-6-( 6-fluoropyridin-3-ylamino )-l,3,5-triazin-2-ylamino )-2-methylprop an-2-ol
Figure imgf000130_0001
1H NMR (METHANOL-d4) δ 8.58 (s, IH), 8.42-8.31 (m, 2H), 8.00-7.98 (m, IH), 7.63-7.61 (m, IH), 7.09-7.08 (m, IH), 3.52 (s., 2H), 1.27 (s., 6H). LC-MS: m/z 390.2 (M+H)
Compound 389 - l-(4-(6-chloropyridin-2-yl)-6-(2-(trifluoromethyl)pyridin-4-ylamm
pan-2-ol
Figure imgf000130_0002
1H NMR (METHANOL-d4) δ 8.46-7.92 (m, 3H), 7.91-7.52 (m, 3H), 3.98-3.88 (m, IH), 3.52-3.33 (m, 2H), 1.16 (t, J = 8.0 Hz, 6H). LC-MS: m/z 426.2 (M+H).
Compound 390 - l-( 4-( 6-chloropyridin-2-yl)-6-( 5-fluoropyridin-3-ylamino )-l,3,5-triazin-2-ylamino )-2-methylprop -2-ol
Figure imgf000130_0003
1H NMR (METHANOL-d4) δ 8.72 (s, IH), 8.63-8.43 (m, 2H), 8.16-8.16 (m, IH), 8.03-7.99 (m, IH), 7.65-7.64 (m, IH), 3.57 (s, 2H), 1.30 (s, 6H). LC-MS: m/z 390.2 (M+H).
Compound 391 - l-(4-(6-chloropyridin-2-yl)-6-{2-(trifluoromethyl)pyridin-4-y
methylpropan-2-ol
Figure imgf000130_0004
1H NMR (METHANOL-d4) δ 8.62-8.17 (m, 3H), 8.00-7.95 (m, IH), 7.84-7.83 (m, IH), 7.63-7.61 (m, IH), 3.56 (s, 2H), 1.28 (s, 6H). LC-MS: m/z 440.3 (M+H).
Compound 393 -
6-(6-chloropyridin-2-yl)-N2-(2-fluoropyridin-4-yl)-N4-(oxetan-3-yl)-l,3,5-tria^
Figure imgf000131_0001
1H NMR (DMSO-d6): δ 10.6-10.8 (m, 2H), 8.8-9.2 (m, IH), 8.3-8.5 (m, IH), 7.9-8.2 (m, 2.4H), 7.6-7.8 (m, 2.5H), 5.0-5.2 (m, IH), 4.75(m, 2H), 4.6(m, 2H). LC-MS: m/z 373 (M+H)+.
Compound 394 -
6-(6-chloropyridin-2-yl)-N2 sopropyl-N4-(5-(trifluoromethyl)pyridin-^
mine
Figure imgf000131_0002
1H NMR (METHANOL-d4) δ 9.15-8.70 (s, 2H), 8.49 (s, IH), 8.43-8.38 (m, IH), 7.98-7.93 (m, IH), 7.60-7.58 (m, IH), 4.50-4.18 (m, IH), 1.30 (d, J = 8 Hz, 6H). LC-MS: m/z 410.2 (M+H)+. Compound 396 -
6-(6-chloropyridin-2-yl)-N2 sopropyl-N4-(2-(trifluoromethyl)pyridin-4-yl^^
mine
Figure imgf000131_0003
1H NMR (METHANOL-d4) δ 8.86-8.67 (br.s, IH), 8.48-8.42 (m, 2H), 8.23-7.61 (m, 3H), 4.53-4.13 (m, IH), 1.32 (s, 6H). LC-MS: m/z 410.2 (M+H)+.
Compound 399 -
6-(6-chloropyridin-2-yl)-N2-(5-fluoropyridin-3-yl)-N4 sobutyl-l,3,5-triazine-2^
Figure imgf000132_0001
IH NMR (METHANOL-d4) δ 8.67-8.41 (m, 3H), 8.13-8.10 (m, IH), 8.00-7.97 (m, IH), 7.96-7.62 (m, IH), 3.42-3.31 (m., 2H), 2.04-2.01 (m., IH), 1.00 (dd, J = 4, 400 MHz, 6H). LC-MS: m/z 374.2 (M+H)+.
Compound 400 -
N2-(3-(azetidin-l-ylsulfonyl)phenyl)-6-(6-chloropyridin-2-yl)-lS^
mine
Figure imgf000132_0002
1H NMR (METHANOL-d4) δ 8.93 (s, IH), 8.47-8.45 (m, IH), 7.98 (m, IH), 7.63-7.61 (m, IH), 7.56 (m, 2H), 7.50-7.48 (m, IH), 4.35 (m, IH), 3.82-3.78 (m., 4H),2.1-2.06 (m., 2H), 1.32-1.30 (d, J = 8 Hz, 6H). LC-MS: m/z 459.9 (M+H)+.
Compound 401 - -(4-(isopropylamino)-6-(6-(trifluoromethyl)pyridin-2-yl)-l,3,5-triazin-2-yla
Figure imgf000132_0003
1H NMR (METHANOL-d4) δ: 8.96-8.84 (m, 2 H), 8.59-8.54 (m, 1 H), 8.42-8.397 (m,l H), 8.11-8.07(m ,1 H), 7.87-7.85 (d, J = 8.0 Hz, 1 H),4.47-4.12 (m, 1 H), 1.21 (d, J = 6.8 Hz, 6 H). LC-MS: m/z 401.2 (M+H)+.
Compound 402 -
N2-(2-fluoropyridin-4-yl)-l^-((tetrahydrofuran-2-yl)methyl)-6-(6-(trifluo
l,3,5-triazine-2,4-diamine
Figure imgf000133_0001
1H NMR (METHANOL-d4) δ: 8.69 (t, J = 7.4 Hz, 1 H), 8.22 (t, J = 8.0 Hz„ 1 H), 8.04-7.98 (m,2 H), 7.84 (s, 1 H), 7.53 (dd, J = 10.8 Hz, 5.2 Hz, IH), 4.23-4.19 (m, 1 H), 3.99-3.96 (m, 1 H), 3.83-3.78 (m, 1 H), 3.70-3.63 (m, 2 H), 2.12-2.08 (m, IH), 2.04-1.95 (m, 2H), 1.79-1.72 (m, IH). LC-MS: m/z 436.2 (M+H)+.
Compound 403 -
4-( 4-( ( tetrahydrofuran-2-yl)methylamino )-6-( 6-( trifluoromethyl)pyridin-2-yl)-l,3,5-triazin-2-yla mino )picolinonitrile
Figure imgf000133_0002
1H NMR (METHANOL-d ) δ: 8.68 (t, J = 7.2 Hz, 1 H), 8.59 (d, J = 16.8 Hz„ 1 H), 8.46 (dd, J = 14.0 Hz, 5.8 Hz, 2 H), 8.21 (t, J = 7.8 Hz, IH), 7.99-7.95 (m, 2H), 4.23-4.20 (m, 1 H), 3.99-3.93 (m, 1 H), 3.84-3.78 (m, 1 H), 3.69-3.62 (m, 2 H), 2.13-2.09 (m, IH), 2.05-1.98 (m, 2H), 1.79-1.73 (m, IH). LC-MS: m/z 443.3 (M+H)+.
Compound 404 - -(4-(isopropylamino)-6-(6-(trifluoromethyl)pyridin-2-yl)-l,3,5-triazin-2-yla
Figure imgf000133_0003
1H NMR (METHANOL-d ) δ: 8.72-8.65 (m, IH), 8.59 (s, 1 H), 8.48 (dd, J = 10.4 Hz, 6.0 Hz, 1 H), 8.22 (t , J = 7.8 Hz, 1 H), 7.99-7.94 (m, 2 H),4.49-4.25 (m, 1 H), 1.31 (d, J =7.6 Hz, 6 H). LC-MS: m/z 401.2 (M+H)+.
Compound 405 -
5-(4-(2-hydroxy-2-methylpropylamino)-6-(6-(trifluoromethyl)pyridin-2-yl)-l,3,5 riaz no )nicotinonitrile
Figure imgf000134_0001
1H NMR (METHANOL-d4) δ 9.03-9.12 (m, 1 H), 8.70-8.78 (m, 3 H), 8.37-8.45 (m, 1 H), 8.18-8.25 (d, J = 7.2 Hz, 1 H), 3.62 (s, 2 H), 1.35 (s, 6 H). LC-MS: m/z 431.1 (M+H)+.
Compound 406 -
2-methyl-l-(4-(6-(trifluoromethyl)pyridin-2-yl)-6-(5-(trifluoromethyl)pyrid^
ίαζίη-2-ylamino )propan-2-ol
Figure imgf000134_0002
1H NMR (METHANOL-d4) δ 9.00-9.18 (m, 2 H), 8.69-8.71 (m, 1 H), 8.51-8.54 (m, 1 H), 8.20-8.22 (m, 1 H), 7.98-8.00 (m, 1 H), 3.57-3.65 (d, J = 30.8 Hz, 2 H), 1.30 (s, 6 H). LC-MS: m/z 474.2 (M+H)+.
Compound 407 - l-(4-(5-fluoropyridin-3-ylamino)-6-(6-(trifluoromethyl)pyridin-2-yl)-l,3,5-trw^
methylpropan-2-ol
Figure imgf000134_0003
1H NMR (METHANOL-d4) δ 8.92 (s, 1 H), 8.81-8.83 (m, 1 H),8.53-8.58 (m, 3 H), 8.26-8.28 (m, 1 H), 3.64 (s, 2 H), 1.35 (s, 6 H). LC-MS: m/z 424.2 (M+H)+.
Compound 408 -
4-( 4-( isobutylamino )-6-( 6-( trifluoromethyl)pyridin-2-yl)-l,3,5-triazin-2-ylamino )picolinonitrile
Figure imgf000134_0004
1H NMR (DMSO-d4) δ 10.7 (s, 1 H), 8.52-8.70 (m, 4 H), 8.30-8.34 (m, IH), 8.11-8.13 (m, 1 H), 7.93-8.05 (m, 1 H), 3.21-3.24 (q, J = 6.4 Hz, 2 H), 1.95-2.00 (m, 1 H), 0.96-0.98 (q, J = 3.6 Hz, 6H). LC-MS: m/z 415.3 (M+H)+.
Compound 409 -
2-methyl-l-(4-(6-(trifluoromethyl)pyridin-2-yl)-6-(2-(trifluoromethyl)pyri^
ίαζίη-2- lamino ropan-2-ol
Figure imgf000135_0001
1H NMR (METHANOL-d4) δ 8.62-8.68 (m, 2 H), 847-8.50 (m, 1 H), 8.18-8.21 (m, 1 H), 7.96-7.98 (m, 1 H), 7.82-7.84 (m, 1 H), 3.56-3.63 (d, J = 28 Hz, 2 H), 1.30 (s, 6 H). LC-MS: m/z 474.3 (M+H)+.
Compound 410 - -(6-chloropyridin-2-yl)-N2-(6-fluoropyridin-3-yl)-N4-(oxetan-3-yl)-l,3,5-tria^
Figure imgf000135_0002
IH NMR (METHANOL-d4) δ 8.50-8.31 (m, 3H), 7.89-7.86 (m, IH), 7.53-7.51 (m, IH), 7.02-7.00 (m, IH), 5.02-4.90 (m., IH), 4.88-4.84 (m., 2H), 4.61-4.59 (m, 2H)
LC-MS: m/z 374.2 (M+H)+.
Compound 411 -
N2-(3-oxabicyclo[3J ]hexan-6-yl)-N4-(5-fluoropyridin-3-yl)-6-(6-(trifluoromethyl)pyrM - -triazine-2,4-diamine
Figure imgf000135_0003
1H NMR (DMSO-d6) δ 10.04-10.06 (m, 1H), 8.69-8.91 (m, 1H), 8.47-8.58 (m, 2H), 8.32 (t, J = 8.0 Hz, 1H), 8.19-8.24 (m., 1H), 8.10-8.12 (m, 1H), 3.98 (d., J = 8.0 Hz, 2H), 3.69 (d., J = 8.0 Hz, 2H), 2.57-2.61 (m, 1H), 1.97 (s, 2 H). LC-MS: m/z 434.2 (M+H)+.
Example 4. Preparation of Compounds of Formula I Wherein Ring A is Substituted Phenyl.
The compounds of this Example are prepared by general Scheme 4, set forth below.
Scheme 4
Figure imgf000136_0001
Formula I
Example 4, step 1: Preparation of 4,6-dichloro-N-isopropyl-l,3,5-triazin-2-amine. To a solution of 2,4,6-trichloro-l,3,5-triazine (4.0 g, 0.0217 mol) in THF (25 mL) was added isopropyl amine (1.27 g, 0.0217 mmol) at 0°C. The mixture was stirred at room temperature for 12 hours. The mixture was adjusted pH 7 by aq NaHC03 and extracted with ethyl acetate (100 mL*2). The combined organic layer was dried over Na2S04, concentrated and purified by column
chromatography to give 4,6-dichloro-N-isopropyl-l,3,5-triazin-2-amine as a colorless oil.
Figure imgf000136_0002
H NMR (CDC13) δ 1.24-1.27 (m, 6H), 4.21-4.26 (m, 1H), 5.68 (br s, 1H). The following intermediates (13) were prepared following the procedure of Step 1 using the appropriate amine 6.
4,6-dichloro-N-(oxetan-3-yl)-l,3,5-triazin-2-amine, which was directly used in the next step.
CI
N^N ^ H
1H NMR (CDC13) δ 1.71-1.83 (m, 2H), 1.90-2.04 (m, 2H), 2.37-2.46 (m, 2H), 4.46-4.56 (m, 1H), 6.04 (br. 1H).
l-(4,6-Dichloro-[l,3,5]triazin-2-ylamino)-2-methyl-propan-2-ol, which was directly used in the next step.
Figure imgf000137_0001
LCMS: m/z 237.0 (M+H)+.
4,6-dichloro-N-isobutyl-l,3,5-triazin-2-amine, which was directly used in the next step.
Figure imgf000137_0002
1H NMR (CDCI3) δ 0.85 (d, J = 8.6 Hz, 6H), 1.75-1.94 (m, 1 H), 3.30-3.33 (m, 2H), 6.29 (br, 1H).
Example 4, step 2: Preparation of l-[4-chloro-6-(2-fluoro-phenyl)-[l,3,5]
triazin-2-ylamino]-2-methyl-propan-2-ol. To a mixture of
4,6-dichloro-N-isopropyl-l,3,5-triazin-2-amine (1.0 g, 4.83 mmol), 3-fluorophenylboronic acid (0.671 g, 0.00483 mol) and Cs2C03 (3.15 g, 0.00966 mol) in dioxane/water (12 mL/2.4 mL) was added Pd(PPh3)4 (0.56 g, 483 mmol). The mixture was heated to 80°C for 2 hours. The mixture was concentrated and purified by Si02 chromatography to give
l-[4-chloro-6-(2-fluoro-phenyl)-[l,3,5] triazin-2-ylamino]-2-methyl-propan-2-ol as a white solid.
Figure imgf000138_0001
LCMS: m/z 297.1 (M+H)+.
Additional intermediates 15 were prepared by the method of Example 4, step 2 using the appropriate boronic acid 14 and the appropriate starting intermediate 13.
loro-phenyl)- [l,3,5]triazin-2-yl]-isopropyl-amine
Figure imgf000138_0002
LCMS: m/z 282.9 (M+H)+.
4-chloro-6-(2-fluorophenyl)-N-isopropy l-l,3,5-triazin-2-
Figure imgf000138_0003
LCMS: m/z 266.8 (M+H)+.
lorophenyl)-N- isopropyl-l,3,5-triazin-2-
Figure imgf000138_0004
LCMS: m/z 282.8 (M+H)+.
4-chloro-6-(3-fluorophenyl)-N- isopropyl-l,3,5-triazin-2-
Figure imgf000139_0001
LCMS: m/z 266.9 (M+H)+.
[3-(4-Chloro-6-isopropylamino-[l,3,5] triazin-2-yl)-phenyl]-carbamic acid tert-butyl ester
Figure imgf000139_0002
LCMS: m/z 364.2 (M+H)+.
-Chloro-6-(3-methoxy-phenyl)- [l,3,5]triazin-2-yl]-isopropyl-
Figure imgf000139_0003
LCMS: m/z 279.1 (M+H)+.
Example 4, step 3 (Procedure A): Preparation of Compound 227 - 6-(2-fluorophenyl)-N2 sopropyl-I^-(pyridin-4-yl)-l,3,5-triazine-2,4-diamine.
A mixture of 4-chloro-6-(2-fluorophenyl)-N-isopropyl-l,3,5-triazin-2-amine (290 mg, 1.1 mmol), pyridine-4-amine (103 mg, 1.1 mmol), CsF (554 mg, 2.2 mmol) and DIPEA (0.425 g, 3.3 mmol) in DMSO (4 mL) was heated to 80°C for 2 hours. The mixture was filtered and purified by a
2 4
standard method to give 6-(2-fluorophenyl)-N -isopropyl-N -(pyridin-4-yl)- 1,3,5- e.
Figure imgf000139_0004
1H NMR (METHANOL-d4) δ: 8.32 (t, J = 6.2 Hz, 2H), 8.12-8.03 (m, 1H), 7.89 (t, J = 6.2 Hz, 2H), 7.54-7.49 (m, 1H), 7.27 (t, J = 7.6 Hz, 1H), 7.23-7.18 (m, 1H), 4.35-4.23 (m, 1H), 1.30-1.26 (m, 6H). LC-MS: m/z 325.0 (M+H)+.
The following compound was also made using the procedure of Step 3 and the appropriate amine 4.
(2-chlorophenyl)-N2 sopropyl-N4-(pyridin-4-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000140_0001
1H NMR (METHANOL-d4) δ: 8.31 (t, J = 6.2 Hz, 2H), 7.87 (t, J = 6.2 Hz, 2H), 7.74-7.65 (m, 1H), 7.50-7.37 (m, 3H), 4.31-4.26 (m, 1H), 1.30-1.24 (m, 6H). LC-MS: m/z 341.0 (M+H)+.
Example 4, step 3 (Procedure B): Compound 317 -
N2 -cyclobutyl-6-( 2-fluorophenyl)-N4-( 3-( methylsulfonyl)phenyl)-l,3,5-triazine-2,4-diamine
A mixture of [4-chloro-6-(2-fluoro-phenyl)-[l,3,5]triazin-2-yl]-cyclobutyl-amine (150 mg, 0.538 mmol) and 3-methanesulfonyl-phenylamine (l l lmg, 0.648 mmol) in anhydrous THF (10 mL) was stirred at 80°C for 8 hrs. TLC (petroleum ether / ethyl acetate 10/1) indicated the reaction was complete and water was added. The mixture was extracted with ethyl acetate and the organic layer was washed with brine, dried over sodium sulfate. Filtered and the filtrate was concentrated in vacuo to give crude N-cyclobutyl-6-(2-fluoro-phenyl)-N'-(3-methane
-sulfonyl-phenyl)-[l,3,5]triazine-2,4-diamine, which was purified a standard method to give pure -cyclobutyl-6-(2-fluoro-phenyl)-N'-(3-methanesulfonyl-phenyl)-[l,3,5]triazine- 2,4-diamine.
Figure imgf000140_0002
1H NMR (METHANOL-d ) δ: 9.00-8.61 (m, 1H), 8.16-7.76 (m, 1H), 7.62-7.52 (m, 3H), 7.30-7.18 (m, 2H), 4.67-4.61 (m, 1H), 3.16 (s, 3H), 2.52-2.38 (m, 2H), 2.10-2.01 (m, 2H), 1.88-1.76 (m, 2H). LC-MS: m/z 414.3 (M+H)+. Example 4, step 3 (Procedure C): Synthesis of Compound 318 -
N-Cyclobutyl-6-(2-fluoro-phenyl)-N'-(5-fluoro-pyridin-3-yl)-[l,3,5]triazine-2,4-di^ A mixture of [4-chloro-6-(2-fluoro-phenyl)-[l,3,5]triazin-2-yl]-cyclobutyl-amine (300 mg, 1.08 mmol), 5-fluoro-pyridin-3-ylamine (145 mg, 1.29 mmol) Pd(dppf)Cl2 (80 mg, O.l lmmol) and t-BuONa (208 mg, 2.17 mmol) in dioxane (15 mL)was stirred at 80°C under N2 for 2 hrs. Cooled to room temperature and water was added. Extracted with ethyl acetate and the organic layer was washed with brine, dried over sodium sulfate and filtered. The filtrate was concentrated in vacuo and the residue was purified by a standard method to obtain N-cyclobutyl-6-(2-fluoro-phenyl)- '-(5-fluoro-pyridin-3-yl)-[l,3,5]triazine-2,4-diamine.
Figure imgf000141_0001
1H NMR (METHANOL-d4) δ: 8.73-8.44 (m, 2H), 8.08 (d, J = 13.1 Hz, 2H), 7.53 (br.s., 1H), 7.28-7.19 (m, 2H), 4.58-4.51 (m, 1H), 2.42 (br.s., 2H), 2.09 (t, J = 9.6 Hz, 2H), 1.80 (br.s., 2H). LC-MS: m/z 355.2 (M+H)+.
The following compounds were analogously made according to Example 4, step 3 (procedure C) using the appropriate intermediate 15 and the appropriate amine 4
(3-fluorophenyl)-N2-isopropyl-N4-(pyridin-4-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000141_0002
1H NMR (METHANOL-d4) δ: 8.35-8.31 (m, 2H), 8.26-8.20 (m, 1H), 8.10 (t, J = 8.9 Hz, 1H), 7.90 (t, J = 6.9 Hz, 2H), 7.55-7.47 (m, 1H), 7.30-7.24 (m, 1H), 4.43-4.24 (m, 1H), 1.30 (d, J = 6.9 Hz, 6H). LC-MS: m/z 325.0 (M+H)+.
(3-chlorophenyl)-N2 sopropyl-N4-(pyridin-4-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000141_0003
1H NMR (METHANOL-d4) δ: 8.38-8.30 (m, 4H), 7.91-7.87 (m, 2H), 7.53-7.43 (m, 2H),
4.41-4.23 (m, IH), 1.30 (d, J = 6.2 Hz, 6H). LC-MS: m/z 340.9 (M+H)+.
Compound 319 - l-(4-(2-fluorophenyl)-6-(2-(trifluoromethyl)pyridin-4-ylamino)- lpropan-2-ol
Figure imgf000142_0001
1H NMR (METHANOL-d4) δ: 8.65 (s, IH), 8.49-8.38 (m, IH), 8.19-7.85 (m, 2H), Ί .62-1.52 (m, IH), 7.32-7.22 (m, 2H), 3.58-3.56 (m, 2H), 1.29-1.27 (m, 6H). LC-MS: m/z 423.3 (M+H)+.
Compound 392 - l-(4-(2-fluorophenyl)-6-(5-(trifluoromethyl)pyridin-3-ylamino)-l,3,5-triaz
lpropan-2-ol
Figure imgf000142_0002
1H NMR (METHANOL-d ) : δ 8.8-9.1 (m, 2H), 8.48 (m, IH), 8.1 (m, IH), 7.5 (m, IH), 7.2-7.3 (m, 2H), 3.5 (m, 2H), 1.25(m, 6H). LC-MS: m/z 428.3 (M+H)+.
Compound 320 - -(2-fluorophenyl)-N2-(5-fluoropyridin-3-yl)-1^ sobutyl-l,3,5-triazine-2,4-dia
Figure imgf000142_0003
1H NMR (METHANOL-d4) δ: 8.64-8.48 (m, 2H), 8.10-8.04 (m, 2H), 7.55-7.51 (m, IH), 7.29 (t, J = 7.6, IH), 7.29 (t, J = 11.0, IH), 3.32 (br.s., 2H), 2.03-1.96 (m, IH), 1.03-0.96 (m, 6H).
LC-MS: m/z 357.2 (M+H)+.
Compound 321 -
5-( 4-( 2- flu orophenyl )-6-( isopropylam in o )-l,3,5-triazin-2-ylamino )nicotinonitrile
Figure imgf000143_0001
1H NMR (DMSO-d6) δ: 10.25-10.14 (m, IH), 9.14 (t, J = 2.40, IH), 8.89-8.79 (m, IH), 8.62-8.61 (m, IH), 8.04-7.97 (m, 2H), 7.59-7.56 (m, IH), 7.36-7.31 (m, IH), 4.25-4.13 (m, IH), 1.24-1.21 (m, 6H). LC-MS: m/z 350.2 (M+H)+.
Compound 369 - -( 4-( 2- flu orophenyl )-6-( isopropylam in o )-l,3,5-triazin-2-ylamino )picolinonitrile
Figure imgf000143_0002
1H NMR (METHANOL-d4) δ 8.61-8.59 (m, IH), 8.48-8.44 (m, IH), 8.16-8.13 (m, IH), 7.98-7.96 (m, IH), 7.57-7.54 (m, IH), 7.32-7.23 (m., 2H), 4.29-4.27 (m., 2H), 3.05 (s., IH), 1.16 (dd, J = 4, 400 MHz, 6H). LC-MS: m/z 350.2 (M+H)+.
Compound 370 - -(2-fluorophenyl)-N2 sopropyl-I^-(2-(trifluoromethyl)pyridin-4-yl)-l,3,5-tria^
Figure imgf000143_0003
1H NMR (METHANOL-d ) δ 8.65-8.64 (m, 2H), 8.22-8.18 (m, IH), 7.90-7.89 (m, IH), 7.72 (m, 2H), 7.45-7.35 (m., 2H), 4.38-4.35 (m., IH), 1.39 (dd, J = 4, 400 MHz, 6H). LC-MS: m/z 393.0 (M+H)+.
Compound 371 - -(2-fluorophenyl)-N2-(2-fluoropyridin-4-yl)-1^ sopropyl-l,3,5-triazine-2,4-dia
Figure imgf000143_0004
1H NMR (METHANOL-d4) δ 8.20-8.15 (m, 2H), 7.75-7.59 (m, 2H), 7.45-7.38 (m, 3H), 4.37-4.35 (m., IH), 1.37 (dd, J = 4, 400 MHz, 6H). LC-MS: m/z 342.9 (M+H)+.
Compound 372 - -(2-fluorophenyl)-N2 sopropyl-I^-(5-(trifluoromethyl)pyridin-3-yl)-l,3,5-triaz
Figure imgf000144_0001
1H NMR (METHANOL-d ) δ 9.31-8.77 (m, 3H), 8.21 (m, IH), 7.79 (m, IH), 7.47-7.41 (m., 2H), 4.33-4.32 (m, IH), 1.37 (dd, J = 4, 400 MHz, 6H). LC-MS: m/z 393.0 (M+H)+.
Compound 374 - -(2-fluorophenyl)-N2-(5-fluoropyridin-3-yl)-1^ sopropyl-l,3,5-triazine-2,4-dia
Figure imgf000144_0002
1H NMR (METHANOL-d4) δ 8.69-8.61 (m, 2H), 8.12-8.05 (m, 2H), 7.57-7.52 (m, IH), 7.31-7.21 (m., 2H), 4.28-4.25 (m, IH), 1.31 (dd, J = 4, 400 MHz, 6H). LC-MS: m/z 343.2 (M+H)+.
Compound 387 - -(2-fluorophenyl)-N2-(6-fluoropyridin-3-yl)-1^ sopropyl-l,3,5-triazine-2,4-dia
Figure imgf000144_0003
1H NMR (METHANOL-d ) δ 8.61-8.57 (m, IH), 8.42-8.37 (m, IH), 8.04-8.00 (m, IH), 7.55-7.51 (m., IH), 7.30-7.05 (m, 3H), 4.26-4.23 (m, IH), 1.29 (dd, J = 4, 400 MHz, 6H). LC-MS: m/z 342.9 (M+H)+. Preparation of l-[4-(3-Amino-phenyl)-6-(pyridin-4-ylamino)-[l,3,5]triazin-2-yl-
Figure imgf000145_0001
To a mixture of l-[4-(3-N-(BOC-amino)-phenyl)-6-(pyridin-4-ylamino)-
[l,3,5]triazin-2-ylamino]-2-methyl-propan-2-ol (100.2 mg, 0.24 mmol) in ethyl acetate (1 mL) was added HCl/ethyl acetate (4 mL) at 0°C under N2. The mixture was stirred at r.t. for 2 hours. TLC (petroleum ether/ethyl acetate=3: l) showed that the reaction was complete. The mixture was concentrated to give a residue, which was purified by a standard method to give
l-[4-(3-amino-phenyl)-6-(pyridin-4-ylamino)-[l,3,5]triazin-2-ylamino]-2-methyl-propan-2-ol. 1H
NMR (METHANOL-d4) δ: 8.44-8.40 (m, 2H), 8.17-8.12 (m, 2H), 7.83-7.72 (m, 2H), 7.22 (t, J = 7.6 Hz, 2H), 6.92 (d, J = 7.6 Hz, 2H), 4.45-4.26 (m, 1H), 1.31 (d, J = 6.5 Hz, 6H). LC-MS: m/z 322.2 (M+H)+.
Preparation of 3- -Isopropylamino-6-(pyridin-4-ylamino)-[l,3,5]triazin-2-yl]-phenol
Compound 328 -
Figure imgf000145_0002
To a mixture of N-isopropyl-6-(3-methoxy-phenyl)-N'-pyridin-4-yl-[l,3,5]triazine-2,4-diamine (200 mg, 0.6 mmol) in DCM (10 mL) was added BBr3 (60 mg, 0.6 mol) at -78°C under N2. The mixture was allowed to warm to r.t. and stirred for 90 min. before pouring to water (2 mL). After stirring for 20 min. to the mixture was added NaHC03 to adjust pH to 7 and extracted with ethyl acetate. The organic layer was dried over sodium sulphate and concentrated to give a residue, which was purified by a standard method to give 3- [4- isopropylamino-6-(pyridin-4-ylamino)-[l,3,5]triazin-2-yl]-phenol. 1H NMR (DMSO-d6) δ: 11.12-11.05 (m, 1H), 9.72 (br.s., 1H), 8.67-8.60 (m, 2H), 8.38-8.31 (m, 2H), 8.15-8.00 (m, 1H), 7.82-7.74 (m, 2H), 7.32 (t, J = 8.2 Hz, 1H), 7.00 (d, J = 8.2 Hz, 1H), 4.433-4.17 (m, 1H), 1.26-1.22 (m, 6H). LC-MS: m/z 323.2 (M+H)+.
Example 5. Preparation of Compounds of Formula I Wherein Ring A and Ring B are Phenyl. The compounds of this Example are prepared by general Scheme 5, set forth below.
Scheme 5
Figure imgf000146_0001
16 Formula I
Example 5 step 2: Preparation of 4-chloro-N,6-diphenyl-l,3,5-triazin-2-amine . To a solution of 2,4-dichloro-6-phenyl-l,3,5-triazine (1 g, 4.4 mol) in acetone (10 mL) was added dropwise a solution of aniline (0.41 g, 4.4 mol) in acetone (2 mL) at 0°C via syringe under N2. After the addition, the mixture was stirred at 0°C under N2 for 4 hrs. The reaction mixture was adjusted to pH 7 with saturated NaHC03. The cake was dissolved in ethyl acetate (500 ml), dried over anhydrous Na2S04, concentrated and purified via silica gel chromatography to give
4-chloro-N,6-diphenyl-l,3,5-triazin-2-amine as a white solid.
1H NMR (CDC13) δ: 8.42 (d, J = 7.6 Hz, 1H), 8.33 (d, J = 7.6 Hz, 1H), 7.57-7.43 (m, 3H), 5.57-5.49 (m, 1H), 4.42-4.24 (m, 1H), 1.31-1.23 (m, 6H).
Example step 3: Preparation of
2,6-diphenyl-N4-(tetrahydrofuran-3-yl)-l,3,5-triazine-2,4-diamine tetrahydrofuran-3-amine . Compound 203 - To a solution of (4-chloro-6-phenyl-[l,3,5]triazin-2-yl)-phenyl-amine (150 mg, 0.532 mmol) in anhydrous THF (5 mL) was added a solution of l-amino-2-methyl-propan-2-ol (71 mg, 0.796 mmol) in THF (2 mL) via syringe at room temperature and the result mixture was stirred at room temperature for 16 hrs. The reaction was quenched by water (15 mL) and extracted with ethyl acetate. The organic layer was dried over Na2S04, concentrated and purified by a standard method to give pure 2-methyl-l-(4-phenyl-6-phenylamino-[l,3,5]triazin-2-yl- .
Figure imgf000147_0001
1H NMR (METHANOL-d4) δ: 8.35 (t, J = 9.6 Hz, 2H), 7.74 (d, J = 8.2 Hz, 2H), 7.53-7.43 (m, 3H), 7.31 (t, J = 5.5 Hz, 2H), 7.03 (t, J = 7.6 Hz, 1H), 3.56-3.47 (m, 2H), 1.26 (s, 6H). LC-MS: m/z 336.2 (M+H)+.
Other compounds were produced following Example 5, step 3 using the appropriate amine 6.
6-diphenyl-N4-(tetrahydrofuran-3-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000147_0002
1H NMR (METHANOL-d4) δ: 8.39 (br.s., 1H), 8.35 (d, J = 6.9 Hz, 1H), 7.75 (d, J = 7.6 Hz, 3H), 7.52-7.43 (m, 3H), 7.31 (br.s., 2H), 7.02 (t, J = 7.6 Hz, 1H), 4.60 (br.s., 1H), 4.05-3.95 (m, 2H), 3.89-3.83 (m, 1H), 3.76 (dd, J = 8.9, 3.4 Hz, 1H), 2.34-2.29 (m, 1H), 2.04-1.97 (m, 1H). LC-MS: m/z 333.9 (M+H)+.
Compound 175 - N: ' -(oxetan-3-yl)-!S 6-diphenyl-l,3,5-triazine-2,4-diamine
Figure imgf000147_0003
1H NMR (METHANOL-d ) δ: 8.35 (d, J = 7.2 Hz, 2H), 7.71 (br.s., 2H), 7.51-7.41 (m, 3H), 7.30 (br.s., 2H), 7.02 (t, J = 7.2 Hz, 1H), 5.25-5.10 (m, 1H), 4.93 (br.s., 2H), 4.69 (br.s., 2H). LC-MS: m/z 320.0 (M+H)+.
Compound 176 - N2-(3-methyloxetan-3-yl)-N4,6-diphenyl-l,3,5-triazine-2,4-diamine
Figure imgf000148_0001
1H NMR (METHANOL-d4) δ: 8.35 (d, J = 7.6 Hz, 2H), 7.70 (br, 2H), 7.52-7.42 (m, 3H), 7.31 (t, J = 7.6 Hz, 2H), 7.06 (br.s., IH), 4.88 (br.s., 2H), 4.52-4.88 (br.s., 2H), 1.77 (s, 3H). LC-MS: m/z 334.0 (M+H)+.
-methoxyethyl)-N4 ,6-diphenyl-l,3,5-triazine-2,4-diamine
Figure imgf000148_0002
1H NMR (METHANOL-d4) δ: 8.42-8.34 (m, 2H), 7.75 (d, J = 6.9 Hz, 2H), 7.54-7.44 (m, 3H), 7.32 (t, J = 7.6 Hz, 2H), 7.04 (t, J = 7.1 Hz, IH), 3.7-3.58 (m, 4H), 3.41 (s, 3H). LC-MS: m/z 322.0 (M+H)+.
2 -(oxetan-2-ylmethyl)-N4 ,6-diphenyl-l,3,5-triazine-2,4-diamine
Figure imgf000148_0003
1H NMR (METHANOL-d ) δ: 8.40-8.33 (m, 2H), 7.74 (d, J = 8.2 Hz, 2H), 7.52-7.43 (m, 3H), 7.31 (t, J = 8.2 Hz, 2H), 7.02 (t, J = 7.6 Hz, IH), 5.1-5.04 (m, IH), 4.72-4.66 (m, IH), 4.62-4.57 (m, 2H), 3.89-3.68 (m, 2H), 2.71-2.67 (m, IH), 2.61-2.52 (m, IH). LC-MS: m/z 333.9 (M+H)+. Compound 238 - 2-(4-phenyl-6-(phenylamino)-l,3,5-triazin-2-ylamino)ethanol
Figure imgf000148_0004
1H NMR (METHANOL-d ) δ: 8.39-8.31 (m, 2H), 7.75 (d, J = 7.6 Hz, 2H), 7.52-7.43 (m, 3H), 7.31 (t, J = 7.6 Hz, 2H), 7.02 (t, J = 6.9 Hz, IH), 3.76 (t, J = 5.5 Hz, 2H), 3.65-3.59 (m, 2H).
LC-MS: m/z 308.0 (M+H)+. -dimethyl-3-( 4-phenyl- 6- (phenylamin o )-l,3,5-triazin-2-ylamino )propan-l-ol
Figure imgf000149_0001
1H NMR (METHANOL-d4) δ: 8.35-8.29 (m, 2H), 7.74 (t, J = 6.5 Hz, 2H), 7.54-7.44 (m, 3H), 7.32 (q, J = 7.6 Hz, 2H), 7.06-7.01 (m, 1H), 3.39 (d, J = 9.5 Hz, 2H), 3.22 (s, 2H), 0.94 (s, 6H).
LC-MS: m/z 350.1 (M+H)+.
Compound 240 - l-(4-phenyl-6-(phenylamino)-l,3,5-triazin-2-ylamino)propan-2-ol
Figure imgf000149_0002
1H NMR (METHANOL-d4) δ: 8.39-8.32 (m, 2H), 7.74 (d, J = 7.8 Hz, 2H), 7.52-7.43 (m, 3H), 7.31 (t, J = 7.8 Hz, 2H), 7.02 (t, J = 7.1 Hz, 1H), 4.06-3.98 (m, 1H), 3.56-3.33 (m, 2H), 1.22 (d, J 6.4 Hz, 3H). LC-MS: m/z 321.9 (M+H)+.
enyl-6-(phenylamino)-l,3,5-triazin-2-ylamino)propan-l-ol
Figure imgf000149_0003
1H NMR (METHANOL-d4) δ: 8.39-8.32 (m, 2H), 7.74 (d, J = 7.6 Hz, 2H), 7.52-7.42 (m, 3H), 7.30 (t, J = 7.6 Hz, 2H), 7.02 (t, J = 7.6 Hz, 1H), 4.37-4.25 (m, 1H), 3.65-3.58 (m, 2H), 1.27 (d, J 6.9 Hz, 3H). LC-MS: m/z 322.0 (M+H)+.
Compound 242 - 3-methyl-2-(4-phenyl-6-(phenylamino)-l,3,5-triazin-2-ylamino)butan-l-ol
Figure imgf000149_0004
1H NMR (METHANOL-d4) δ: 8.41-8.33 (m, 2H), 7.75 (d, J = 8.0 Hz, 2H), 7.52-7.44 (m, 3H), 7.31 (t, J = 7.6 Hz, 2H), 7.03 (t, J = 7.6 Hz, 1H), 4.25-4.05 (m, 1H), 3.73 (d, J = 4.8 Hz, 2H), 2.12-2.02 (m, 1H), 1.04-1.00 (m, 3H). LC-MS: m/z 350.1 (M+H)+.
-3-(4-phenyl-6-(phenylamino)-l,3,5-triazin-2-ylamino)cyclopentanol
Figure imgf000150_0001
1H NMR (METHANOL-d ) δ: 8.42-8.32 (m, 2H), 7.80-7.75 (m, 2H), 7.52-7.42 (m, 3H), 7.33-7.29 (m, 2H), 7.01 (t, J = 7.2 Hz, 1H), 4.63-4.58 (m, 1H), 4.39-4.36 (m, 1H), 2.32-2.25 (m, 1H), 2.10-2.03 (m, 2H), 1.84-1.78 (m, 1H), 1.69-1.52 (m, 2H). LC-MS: m/z 348.1 (M+H)+.
6-diphenyl-N4-(tetrahydro-2H-pyran-3-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000150_0002
1H NMR (METHANOL-d ) δ: 8.43-8.36 (m, 2H), 7.77 (t, J = 7.6 Hz, 2H), 7.55-7.45 (m, 3H), 7.34 (t, J = 7.6 Hz, 2H), 7.05 (t, J = 7.2 Hz, 1H), 4.26-4.05 (m, 2H), 3.86-3.83 (m, 1H), 3.55-3.50 (m, 1H), 3.40-3.33 (m, 1H), 2.15-2.06 (m, 1H), 1.87-1.66 (m, 3H). LC-MS: m/z 348.1 (M+H)+. Compound 269 - N2 -(l-methoxypropan-2-yl)-lS 6-diphenyl-l,3,5-triazine-2,4-diamine
Figure imgf000150_0003
1H NMR (METHANOL-d ) δ: 8.41-8.35 (m, 2H), 7.78 (d, J = 7.2 Hz, 2H), 7.55-7.45 (m, 3H), 7.33 (t, J = 7.6 Hz, 2H), 7.05 (t, J = 7.2 Hz, 1H), 4.54-4.37 (m, 1H), 3.58-3.55 (m, 1H), 3.46-3.41 (m, 1H), 3.41 (s, 3H), 1.30 (d, J = 6.9 Hz, 3H). LC-MS: m/z 336.1 (M+H)+.
Compound 296 -
N2-((lS,2R,4R)-bicyclo[2.2 ]heptan-2-yl)-l^,6-diphenyl-l,3,5-triazine-2,4-di^
Figure imgf000151_0001
1H NMR (DMSO-d6) δ: 9.60-9.47 (m, 1H), 8.36-8.30 (m, 2H), 7.89-7.84 (m, 2H), 7.80-7.61 (m, 1H), 7.56-7.50 (m, 3H), 7.31 (t, J = 7.6 Hz, 2H), 6.70 (t, J = 6.9 Hz, 1H), 4.30-4.15 (m, 1H), 2.32-2.25 (m, 1H), 2.07-1.90 (m, 1H), 1.65-1.1 (m, 8H). LC-MS: m/z 358.1 (M+H)+.
Compound 352 - (lS,2R)-2-(4-phenyl-6-(phenylamino)-l,3,5-triazin-2-ylamino)cyclopentanol
Figure imgf000151_0002
1H NMR (METHANOL-d4) δ: 8.42-8.32 (m, 2H), 7.77 (t, J = 7.9 Hz, 2H), 7.56-7.46 (m, 3H), 7.34 (t, J = 7.6 Hz, 2H), 7.05 (t, J = 7.2 Hz, 1H), 4.42-4.23 (m, 2H), 2.17-2.10 (m, 1H), 1.99-1.87 (m, 2H), 1.80-1.70 (m, 3H). LC-MS: m/z 348.2 (M+H)+.
henyl-6-(phenylamino)-l,3,5-triazin-2-ylamino)cyclohex-2-enone
Figure imgf000151_0003
1H NMR (METHANOL-d4) δ: 8.47 (d, J = 7.6 Hz, 1H), 7.78 (br.s., 2H), 7.60-7.50 (m, 3H), 7.39 (t, J = 8.2 Hz, 2H), 7.23 (br.s., 1H), 7.12 (t, J = 7.6 Hz, 1H), 2.75 (t, J = 6.2 Hz, 2H), 2.43 (t, J = 6.2 Hz, 2H), 2.12-2.03 (m, 2H). LC-MS: m/z 358.2 (M+H)+.
Example 6. Preparation of Additional Compounds of Formula I Wherein Ring A is Phenyl.
The compounds of this Example are prepared by general Scheme 6, set forth below.
Figure imgf000152_0001
Formula I
Example 6, step 2: Preparation of tert-Butyl-(4-chloro-6-phenyl-[l,3,5]triazin-2-yl)-amine
To a solution of 2,4-dichloro-6-phenyl-l,3,5-triazine (500 mg, 2.212 mmol) in anhydrous THF (4 mL) was added dropwise a solution of tert-butylamine (194.1 mg, 2.654 mol) in THF (1 mL) at room temperature via syringe under N2. After the addition, the mixture was stirred at room temperature under N2 for 2 hrs. The reaction was quenched by water (5 mL) and extracted with ethyl acetate. The organic layer was dried, concentrated to afford
tert-butyl-(4-chloro-6-phenyl-[l,3, and 5]-triazin-2-yl)-amine as a white solid, which was used the directly in the next step without purification.
Other amines 6 were also employed using the standard procedure described above to give the desired intermediates and were also used in the next step directly without further purification. Example 6, step 3: Preparation of Compound 227
6-(2-fluorophenyl)-N2 sopropyl-I^-(pyridin-4-yl)-l,3,5-triazine-2,4-diamine. A mixture of tert-butyl-(4-chloro-6-phenyl-[l, 3, and 5] triazin-2-yl)-amine (186.1 mg, 0.71 mmol), pyridines- amine (80 mg, 0.85 mmol), CsF (107.85 mg, 0.71 mmol) and DIEA (275.30 mg, 2.13 mmol) in DMSO (4 mL) was heated to 80°C for 2 hours. The mixture was filtered and purified by a standard method to give 6-(2-fluorophenyl)-N 2 -isopropyl-N 4 -(pyridin-4-yl)-l,3,5-triazine-2,4-diamine. This compound was also produced by Step 3, procedure A of Example 4. Additional compounds of one aspect of the invention are produced according to Scheme 6 and the methods set forth in this example using the appropriate amine 6 and the appropriate amine 4.
-sec-butyl-6-phenyl-N4-(pyridin-4-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000153_0001
1H NMR (METHANOL-d4) δ: 8.44-8.33 (m, 4H), 7.92 (m, 2H), 7.54 (t, J = 7.14 Hz, 1H), 7.48 (t, J = 7.14 Hz, 2H), 4.30-4.09 (m, 1H), 1.66 (m, 2H), 1.28 (d, J = 6.56 Hz, 3H), 1.02 (t, J = 7.29 Hz, 3H). LC-MS: m/z 321.1 (M+H)+.
Compound 287 - N2-cyclopentyl-6-phenyl-N4-(pyridin-4-yl)-l,3,5-tr zine-2,4-diamine
Figure imgf000153_0002
1H NMR (DMSO-d6) δ: 8.43-8.37 (m, 4H), 8.06-8.02 (m, 2H), 7.52-7.46 (m, 3H), 4.52-4.36 (m,
1H), 2.08 (m, 2H), 1.80-1.62 (m, 6H). LC-MS: m/z 333.1 (M+H)+.
cyclobutyl-6-phenyl-N4-(pyridin-4-yl)-l,3,5-tr zine-2,4-diamine
Figure imgf000153_0003
1H NMR (DMSO-d6) δ: 8.50-8.30 (m, 4H), 8.00-7.90 (m, 2H), 7.60-7.40 (m, 3H), 4.55 (m, 1H),
2.45 (m, 2H), 2.10 (m, 2H), 1.80 (m, 2H). LC-MS: m/z 319.1 (M+H)+.
Compound 189 - N2-tert-butyl-6^henyl-l^-(pyridin-4-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000153_0004
1H NMR (DMSO-d6) δ: 8.50-8.30 (m, 4H), 8.00-7.90 (m, 2H), 7.60-7.40 (m, 3H), 1.56 (m, 9H). LC-MS: m z 321.1 (M+H)+.
isobutyl-6-phenyl-N4-(pyridin-4-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000154_0001
1H NMR (METHANOL-d4) δ: 8.35-8.21 (m, 4H), 7.84-7.78 (m, 2H), 7.48-7.34 (m, 3H), 3.30 (d, J = 2.0 Hz, 2H), 1.96-1.87 (m, 1H), 0.92 (d, J = 6.8 Hz, 6H). LC-MS: m/z 321.0 (M+H)+.
2-neopentyl-6-p enyl-l^-(pyridin-4-yl) ,3,5-tr zine-2,4-d mine
Figure imgf000154_0002
1H NMR (METHANOL-d ) δ: 8.57-8.52 (m, 1H), 8.43-8.28 (m, 4H), 7.60-7.37 (m, 3H), 3.36 (d, J = 2.0 Hz, 2H), 0.94 (d, J = 9.6 Hz, 9H). LC-MS: m/z 335.1 (M+H)+.
Compound 211 - N2-butyl-6-phenyl-N4-(pyridin-4-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000154_0003
1H NMR (METHANOL-d4) δ: 8.37-8.25 (m, 4H), 7.84 (d, J = 6.41 Hz, 2H), 7.46 (t, J = 7.12 Hz, 1H), 7.40 (t, J = 7.12 Hz, 2H), 3.50-3.41 (m, 2H), 1.61 (m, 2H), 1.40 (m, 2H), 0.93 (t, J = 7.23 Hz, 3H). LC-MS: m/z 321.0 (M+H)+.
Compound 212 - N2 sopentyl-6-phenyl-N4-(pyridin-4-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000154_0004
1H NMR (METHANOL-d4) δ: 8.30-8.18 (m, 4H), 7.77 (d, J = 5.98 Hz, 2H), 7.41-7.31 (m, 3H), 3.45-3.36 (m, 2H), 1.60 (m, 1H), 1.45 (m, 2H), 0.86 (d, J = 6.52 Hz, 3H). LC-MS: m/z 335.1 (M+H)+.
Compound 213 - N2-{3-methylbutan-2-yl)-6-p enyl-l^-(pyruiin-4-yl)-l,3,5-tr z
Figure imgf000155_0001
1H NMR (METHANOL-d4) δ: 8.33-8.23 (m, 4H), 7.85-7.80 (m, 2H), 7.44 (t, J = 7.03 Hz, 1H), 7.38 (t, J = 7.03 Hz, 2H), 4.14-3.97 (m, 1H), 1.83 (m, 1H), 1.14 (d, J = 6.69 Hz, 3H), 0.94-0.90 (m, 6H). LC-MS: m/z 335.1 (M+H)+.
Compound 215 - 6-phenyl-N2-(pyridin-4-yl)-N4-( 2,2,2-trifluoroethyl)-l,3,5-triazine-2,4-diamine
Figure imgf000155_0002
1H NMR (METHANOL-d4) δ: 8.44 (m, 2H), 8.36 (m, 2H), 7.90 (m, 2H), 7.55 (t, J = 7.32 Hz, 1H), 7.48 (t, J = 7.32 Hz, 2H), 4.35-4.20 (m, 2H). LC-MS: m/z 346.9 (M+H)+.
( cyclopropylmethyl)-6-phenyl-N4-(pyridin-4-yl)-l,3,5-tr zine-2,4-d mine
Figure imgf000155_0003
1H NMR (METHANOL-d4) δ: 8.43-8.32 (m, 4H), 7.91 (m, 2H), 7.53 (t, J = 7.21 Hz, 1H), 7.47 (t, J = 7.21 Hz, 2H), 3.43-3.36 (m, 2H), 1.18 (m, 1H), 0.54 (m, 2H), 0.32 (m, 2H). LC-MS: m/z 319.0 (M+H)+.
cyclopropyl-6-phenyl-l^-(pyridin-4-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000155_0004
1H NMR (METHANOL-d4) δ: 8.46-8.33 (m, 4H), 8.01-7.91 (m, 2H), 7.54-7.44 (m, 3H),
2.88-2.99 (m, 1H), 0.87 (m, 2H), 0.64 (m, 2H). LC-MS: m/z 305.0 (M+H)+.
Compound 218 - N2-( l-methylcyclopropyl)-6^henyl-I^-(pyridin-4-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000156_0001
1H NMR (METHANOL-d4) δ: 8.51-8.33 (m, 4H), 8.05-7.90 (m, 2H), 7.54-7.44 (m, 3H), 1.54 (s, 3H), 0.91-0.77 (m, 4H). LC-MS: m/z 319.0 (M+H)+.
Compound 219 - N2-(2-methylcyclopropyl)-6^henyl-l^-(pyridin-4-yl)-l,3,5-triazine-2,4-dM
Figure imgf000156_0002
1H NMR (METHANOL-d4) δ: 8.57-8.40 (m, 4H), 7.98-8.09 (m, 2H), 7.59 (t, J = 7.23 Hz, 1H), 7.53 (t, J = 7.23 Hz, 2H), 2.66 (m, 1H), 1.29 (d, J = 5.43 Hz, 3H), 1.05 (m, 1H), 0.91 (m, 1H), 0.70 (m, 1H). LC-MS: m/z 319.2 (M+H)+.
-methylbutyl)-6^henyl-N4-(pyridin-4-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000156_0003
1H NMR (METHANOL-d4) δ: 8.47 (m, 2H), 8.39 (d, J = 5.80 Hz, 2H), 7.97 (m, 2H), 7.59 (t, J = 6.44 Hz, 1H), 7.53 (t, J = 6.44 Hz, 2H), 3.58-3.29 (m, 2H), 1.85 (m, 1H), 1.60 (m, 1H), 1.32 (m, 1H), 1.06-1.02 (m, 6H). LC-MS: m/z 335.2 (M+H)+.
Compound 221 -
N2-{{2-methyltetra ydrofuran-2-yl)methyl)-6-p enyl-l^-(pyruiin-4-y^
e
Figure imgf000157_0001
1H NMR (METHANOL-d4) δ: 8.51-8.41 (m, 4H), 7.99 (m, 2H), 7.61 (t, J = 7.22 Hz, IH), 7.55 (t, J = 7.22 Hz, 2H), 3.98 (m, 2H), 3.78-3.65 (m, 2H), 2.10 - 1.80 (m, 4H), 1.36 (s, 3H). LC-MS: m/z 363.1 (M+H)+.
Compound 222 - -phenyl-N: ' -(pyridin-4-yl)-]S ^((tetrahydrofuran^-yfymethyi i^^-triazine^^-diamine
Figure imgf000157_0002
1H NMR (METHANOL-d4) δ: 8.53-8.42 (m, 4H), 8.02 (m, 2H), 7.62 (t, J = 7.21 Hz, IH), 7.56 (t, J = 7.21 Hz, 2H), 4.27 (m, IH), 4.01 (m, IH), 3.86 (q, J = 7.23 Hz, IH), 3.75 (m, IH), 3.68 (m, IH), 2.17-1.83 (m, 4H). LC-MS: m/z 349.2 (M+H)+.
Compound 234 - 2-(morpholin-2-ylmethyl)-6^henyl-I^-(pyridin-4-yl)-l,3,5-triazine-2,4-d
Figure imgf000157_0003
1H NMR (METHANOL-d4) δ 8.42 (d, J = 7.2 Hz, IH), 8.39-8.32 (m, 3H), 7.89 (d, J = 4.8 Hz, 2H), 7.51 (d, J = 6.8 Hz, IH), 7.48-7.44 (m, 2H), 3.90-3.87 (m, IH), 3.76-3.74 (m, IH), 3.63-3.52 (m, 3H), 2.99-2.96 (m, IH), 2.81-2.78 (m, 2H), 2.62-2.53 (m, IH). LC-MS: m/z 364.0 (M+H)+. Compound 235 -
6^henyl-N2-(pyridin-4-yl)-I^-(tetrahydrofuran-3-yl)-l,3,5-triazine-2,4-diamm^
Figure imgf000157_0004
1H NMR (DMSO-d6) δ: 9.8-10.0 (m, 1H), 8.1-8.4 (m, 4H), 7.9-8.1 (m, 1H), 7.6-7.8 (m, 2H), 7.3-7.5 (m, 3H), 4.3-4.6 (m, 1H), 3.75-3.85 (m, 1H), 3.7-3.75 (m, 1H), 3.55-3.65 (m, 1H), 3.45-3.55 (m, 1H), 2.0-2.15 (m, 1H), 51.75- 1.85 (m, 1H). LC-MS: m/z 335.1 (M+H)+.
2-(oxetan-3-yl)-6-phenyl-N4-(pyridin-4-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000158_0001
1H NMR (METHANOL-d4) δ: 8.3-8.5 (m, 4H), 7.8-8.0 (m, 2H), 7.45-7.6 (m, 3H), 5.15-5.4 (m, 1H), 5.03 (t, J = 6.8 Hz, 2H), 4.76 (t, J = 6.4 Hz, 2H). LC-MS: m/z 320.9 (M+H)+.
Compound 248 - N2-ethyl-6^henyl-N4-(pyridin-4-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000158_0002
1H NMR (CDC13) δ: 8.50 (m, 2H), 8.43-8.32 (m, 2H), 7.65 (m, 2H), 7.55-7.46 (m, 3H), 7.20-7.08 (m, 1H), 5.45-5.29 (m, 1H), 3.66-3.54 (m, 2H), 1.32 (t, J = 7.25 Hz, 3H). LC-MS: m/z 292.9 (M+H)+.
Compound 249 - 6-phenyl-N2-propyl-N4-(pyridin-4-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000158_0003
1H NMR (METHANOL-d4) δ: 8.46-8.35 (m, 4H), 7.96 (m, 2H), 7.55 (t, J = 7.25 Hz, 1H), 7.49 (t, J = 7.25 Hz, 2H), 3.56-3.45 (m, 2H), 1.73 (m, 2H), 1.05 (t, J = 7.35 Hz, 3H). LC-MS: m/z 307.0 (M+H)+.
2-( cyclobutylmethyl)-6-phenyl-N4-(pyridin-4-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000158_0004
1H NMR (METHANOL-d4) δ: 8.29-8.48 (m, 4H), 7.88-7.95 (m, 2H), 7.49-7.51 (m, 3H), 3.48-3.61 (m, 2H), 2.60-2.75 (m, 1H), 2.08-2.18 (m, 2H), 1.75-2.00 (m, 4H). LC-MS: m/z 332.4 (M+H)+. Compound 251 - N2-(3-methyloxetan-3-yl)-6-phenyl-N4-(pyridin-4-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000159_0001
1H NMR (METHANOL-d4) δ: 8.3-8.5 (m, 4H), 7.8-8.0 (m, 2H), 7.4-7.6 (m, 3H), 4.96 (d, J = 6.4 Hz, 2H), 4.60 (d, J = 6.0 Hz, 2H), 1.81 (s, 3H). LC-MS: m/z 334.9 (M+H)+.
Compound 252 - 2-(2-methoxy-2-methylpropyl)-6-phenyl-N4-(pyridin-4-yl)-l,3,54r zine-2,4-d
Figure imgf000159_0002
1H NMR (METHANOL-d4) δ: 8.30-8.49 (m, 4H), 7.88-7.98 (m, 2H), 7.46-7.51 (m, 3H), 3.62 (s, 1H), 3.70 (s, 2H), 3.30 (s, 3H), 1.25 (s, 6H). LC-MS: m/z 350.43 (M+H)+.
Compound 253 - 2-(3,3-difluorocyclobutyl)-6^henyl-I^-(pyridin-4-yl)-l,3,5-triazine-2,4-d
Figure imgf000159_0003
1H NMR (METHANOL-d4) δ: 8.27-8.18 (m, 4H), 7.73 (m, 2H), 7.37 (t, J = 6.92 Hz, 1H), 7.31 (t, J = 6.92 Hz, 2H), 4.34-4.26 (m, 1H), 2.89 (m, 2H), 2.53 (m, 2H). LC-MS: m/z 354.9 (M+H)+. Compound 254 - 2-(4,4-difluorocyclohexyl)-6-phenyl-N4-(pyridin-4-yl)-l,3,5-tr zine-2,4-d
Figure imgf000159_0004
1H NMR (METHANOL-d4) δ: 8.47-8.35 (m, 4H), 7.93 (m, 2H), 7.56 (t, J = 7.19 Hz, IH), 7.50 (t, J = 7.19 Hz, 2H), 4.28-4.12 (m, IH), 1.76 - 2.18 (m, 8H). LC-MS: m/z 383.1 (M+H)+.
Compound 255 - 2-(3,3-dimethylbutan-2-yl)-6-phenyl-I^-(pyridin-4-yl)-l,3,5-triazine-2,4-d
Figure imgf000160_0001
1H NMR (METHANOL-d4) δ: 8.33-8.42 (m, 4H), 7.91-7.96 (m, 2H), 7.46-7.53 (m, 3H), 1.36 (d, J = 6.4 Hz, IH), 1.21 (d, J = 6.8 Hz, 2H), 1.01 (s, 9H). LC-MS: m/z 349.1 (M+H)+.
enyl-6-(pyridin-4-ylamino)-l,3,5-triazin-2-ylamino)cyclohexanol
Figure imgf000160_0002
1H NMR (METHANOL-d ) δ: 8.56-8.30 (m, 4H), 7.90 (d, J = 5.5 Hz, 2H), 7.53-7.44 (m, 3H), 3.85-4.1 (m, IH), 3.62 (s, IH), 2.15 (s, 2H), 2.03 (s, 2H), 1.46-1.35 (m, 4H). LC-MS: m/z 363.2 (M+H)+.
Compound 257 - N2-( l-cyclopropylethyl)-6^henyl-I^-(pyridin-4-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000160_0003
1H NMR (METHANOL-d ) δ: 8.40-8.34 (m, 4H), 7.94-7.90 (d, J = 16 Hz, 3H), 7.53-7.45 (m, 3H), 4.59 (br.s., IH), 3.75-3.68 (m, IH), 1.36-1.35 (d, J = 4 Hz, IH), 1.05 (br.s., IH), 0.59-0.47 (m, 3H), 0.3 (br.s., IH). LC-MS: m/z 333.2 (M+H)+.
Compound 258 -
6 henyl-N2-(pyridin-4-yl)-N4-(tetrahydro-2H-pyran-4-yl)-l,3,54rw^
Figure imgf000161_0001
1H NMR (METHANOL-d4) δ: 9.38 (m, 2H), 8.54 (m, 2H), 7.65-7.53 (m, 3H), 7.03 (m, 2H), 4.39-4.30 (m, IH), 4.05 (m, 2H), 3.64 (m, 2H), 2.06 (m, 2H), 1.73 (m, 2H). LC-MS: m/z 349.2 (M+H)+.
Compound 259 - -dimethyl-3-( 4-phenyl- 6- ( pyridin - 4-ylam in o )-l,3,5-triazin-2-ylamino )propan-l-ol
Figure imgf000161_0002
1H NMR (METHANOL-d4) δ: 9.38 (m, 2H), 8.54 (m, 2H), 7.65-7.53 (m, 3H), 7.03 (m, 2H), 4.39-4.30 (m, IH), 4.05 (m, 2H), 3.64 (m, 2H), 2.06 (m, 2H), 1.73 (m, 2H). LC-MS: m/z 349.2 (M+H)+.
Compound 262 - N2-(2-ethoxyethyl)-6^henyl-I^-(pyridin-4-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000161_0003
1H NMR (METHANOL-d4) δ: 8.46-8.35 (m, 4H), 7.93-7.91 (d, J = 6 Hz, 2H), 7.55-7.47(m, 3H), 4.93-4.63 (m, 3H), 4.63 (br.s., IH), 3.77-3.70 (m, 4H), 3.62-3.57 (m, 2H), 1.23 (t, J = 6.8 Hz, 3H). LC-MS: m/z 336.9 (M+H)+.
Compound 263 -
6^henyl-N2-(pyridin-4-yl)-N4-(3,3,34rifluoropropyl)-l,3,5-tr zine-2
Figure imgf000161_0004
1H NMR (METHANOL-d4) δ: 8.35-8.47 (m, 4H), 7.90-7.93 (m, 2H), 7.46-7.56 (m, 3H), 3.75-3.82 (m, 2H), 2.57-2.65 (m, 2H). LC-MS: m/z 361.0 (M+H)+.
Compound 264 - N2-( oxetan-2-ylmethyl)-6-phenyl-N4-(pyridin-4-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000162_0001
1H NMR (CDC13) δ: 8.47 (d, J = 5.41 Hz, 2H), 8.36 (m, 2H), 7.63 (m, 2H), 7.52 (t, J = 6.84 Hz, 1H), 7.46 (t, J = 6.84 Hz, 2H), 7.18 (m, 1H), 6.25-5.92 (m, 1H), 5.09 (m, 1H), 4.65 (m, 2H), 3.87 - 3.67 (m, 2H), 2.62 (m, 2H). LC-MS: m/z 335.2 (M+H)+.
Compound 265 - -methyl-l-(4-phenyl-6-(pyridin-4-ylamino)-l,3,5-triazin-2-ylamino)propan-2-ol
Figure imgf000162_0002
1H NMR (CDC13) δ: 8.51 (m, 2H), 8.36 (d, J = 7.70 Hz, 2H), 7.65 (d, J = 4.74 Hz, 2H), 7.55 (t, J = 7.70 Hz, 1H), 7.48 (t, J = 7.70 Hz, 2H), 7.21 (m, 1H), 5.86 (m, 1H), 3.59 (m, 2H), 1.33 (s, 6H). LC-MS: m/z 337.3 (M+H)+.
Compound 271 - l-(4-phenyl-6-(pyridin-4-ylamino)-l,3,5-triazin-2-ylamino)propan-2-ol
Figure imgf000162_0003
1H NMR (METHANOL-d4) δ: 9.38-9.44 (m, 2H), 8.54-8.59 (m, 2H), 7.55-7.64 (m, 3H), 7.01-7.05 (m, 2H), 4.00-4.06 (m, 1H), 3.59-3.67 (m, 2H), 1.29-1.30 (d, J = 6.4 Hz, 3H). LC-MS: m/z 323.1 (M+H)+.
Compound 272 -
N2-(l-methoxypropan-2-yl)-6-phenyl-N4-(pyridin-4-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000163_0001
1H NMR (METHANOL-d4) δ: 8.39-8.45 (m, 4H), 7.97-8.01 (m, 2H), 7.48-7.50 (m, 3H), 4.35-4.62 (m, 1H), 3.57-3.61 (m, 2H), 3.43 (s, 3H), 1.32-1.33 (d, J = 4.0 Hz, 3H). LC-MS: m/z 337.1 (M+H)+.
Compound 273 -
6^henyl-N2-(pyridin-4-yl)-I^-(tetrahydro-2H-pyran-3-yl)-l,3,5-triazine-2,4-d
Figure imgf000163_0002
1H NMR (METHANOL-d4) δ: 9.36-9.41 (m, 2H), 8.53-8.57 (m, 2H), 7.53-7.66 (m, 3H), 7.01-7.05 (m, 2H), 4.17-4.39 (m, 1H), 4.02-4.11 (m, 1H), 3.83-3.91 (m, 1H), 2.10-2.20 (m, 1H), 1.77-1.80 (m, 3H). LC-MS: m/z 349.2 (M+H)+.
Compound 274 - N2-(2-methoxypropyl)-6^henyl-I^-(pyridin-4-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000163_0003
1H NMR (METHANOL-d ) δ: 9.29-9.33 (m, 2H), 8.48-8.52 (m, 2H), 7.52-7.61 (m, 3H), 6.98-7.01 (m, 2H), 3.55-3.78 (m, 3H), 3.44 (s, 3H), 1.26-1.27 (d, J = 4.0 Hz, 3H). LC-MS: m/z 337.2 (M+H)+.
Compound 275 - N2-(3-methoxypropyl)-6^henyl-I^-(pyridin-4-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000163_0004
1H NMR (METHANOL-d4) δ: 8.36-8.41 (m, 4H), Ί .93-1.95 (m, 2H), 7.49-7.51 (m, 3H), 3.54-3.60 (m, 4H), 3.38 (s, 3H), 1.95-1.98 (m, 2H). LC-MS: m/z 337.1 (M+H)+. henyl-6-(pyridin-4-ylamino)-l,3,5-triazin-2-ylamino)cyclobutanone
Figure imgf000164_0001
1H NMR (METHANOL-d4) δ: 8.39-8.44 (m, 4H), 7.97 (s, 2H), 7.48-7.56 (m, 3H), 4.70-4.80 (m,
1H), 3.51-3.58 (m, 2H), 3.20-3.30 (m, 2H). LC-MS: m/z 333.0 (M+H)+.
enyl-6-{pyridin-4-ylamino)-l,3,5-triazin-2-ylamino)propan-l-ol
Figure imgf000164_0002
1H NMR (METHANOL-d4) δ: 9.28-9.33 (m, 2H), 8.46-8.51 (m, 2H), 7.49-7.54 (m, 3H), 6.95-6.99 (m, 2H), 4.30-4.55 (m, 1H), 3.68-3.72 (m, 2H), 1.34 (t, J = 6.8Hz, 1 H). LC-MS: m/z 323.0 (M+H)+.
Compound 279 - 3-methyl-2-(4-phenyl-6-(pyridin-4-ylamino)-l,3,5-triazin-2-ylamino)butan-l-ol
Figure imgf000164_0003
1H NMR (METHANOL-d ) δ: 9.23-9.26 (m, 2H), 8.4 (d, J = 8.0 Hz, 2H), 7.41-7.5 (m, 3H), 6.89 (t, J = 8.0 Hz, 2H), 4.1-4.3 (m, 1H), 3.6-3.8 (m, 1H), 1.9-2.1 (m, 1H), 0.9-1.1 (m.6H). LC-MS: m/z 351.1 (M+H)+.
cyclohexyl-6-phenyl-N4-(pyridin-4-yl)-l,3,5-tr zine-2,4-diamine
Figure imgf000164_0004
1H NMR (METHANOL-d ) δ: 9.34 (t, J = 8.0 Hz, 2H), 8.51 (t, J = 8.0 Hz, 2H), 7.50-7.63 (m, 3H), 6.98-7.03 (m, 2H), 4.0-4.2 (m, 1H), 2.08 (t, J = 12 Hz, 2H), 1.85-1.87 (m, 2H), 1.52-1.53 (m, 1H), 1.28-1.51 (m, 5H). LC-MS: m/z 347.1 (M+H)+. (4-phenyl-6-(pyridin-4-ylamino)-l,3,5-triazin-2-ylamino)cyclohexanol
Figure imgf000165_0001
1H NMR (METHANOL-d4) δ: 9.18 (m 2H), 8.32 (m, 3H), 7.46-7.32 (m, 3H), 6.82 (m, 2H), 4.13-4.02 (m, 1H), 3.96-3.90 (m, 1H), 1.71-1.30 (m, 8H). LC-MS: m/z 363.0 (M+H)+.
Compound 283 - -3-(4-phenyl-6-(pyridin-4-ylamino)-l,3,5-triazin-2-ylamino)cyclopentanol
Figure imgf000165_0002
1H NMR (DMSO-d6) δ: 9.37-9.22 (m, 2H), 9.18 (m, 2H), 8.88-8.69 (m, 1H), 8.54-8.44 (m, 2H), 7.71-7.57 (m, 3H), 7.04 (d, J = 7.85 Hz, 2H), 4.44 (m, 1H), 4.18 (m, 1H), 2.33-1.54 (m, 6H).
LC-MS: m/z 49.1 (M+H)+.
Compound 284 - -( 4-phenyl- 6- ( pyridin-4-ylamin o )-l,3,5-triazin-2-ylamino )cyclobutanecarbonitrile
Figure imgf000165_0003
1H NMR (METHANOL-d4) δ: 8.47 (m, 2H), 8.38 (m, 2H), 7.95 (m, 2H), 7.57 (t, J = 6.74 Hz, 1H), 7.50 (t, J = 6.74 Hz, 2H), 2.88 (m, 2H), 2.57 (m, 2H), 2.22 (m, 2H). LC-MS: m/z 344.0 (M+H)+. Compound 285 - -( 4-phenyl- 6- ( pyridin-4-ylamin o )-l,3,5-triazin-2-ylamino )cyclopropanecarbonitrile
Figure imgf000165_0004
1H NMR (METHANOL-d4) δ: 9.46-9.35 (m, 2H), 8.71-8.55 (m, 2H), 7.70-7.54 (m, 3H), 7.09-7.01 (m, 2H), 1.75 (m, 2H), 1.46 (m, 2H). LC-MS: m/z 330.0 (M+H)+.
Compound 286 -
3,3-dimethyl-2-( 4-phenyl- 6- ( pyridin - 4-ylam in o )-l,3,5-triazin-2-ylamino )butan-l-ol
Figure imgf000166_0001
1H NMR (METHANOL-d4) δ: 9.43 (m, 2H), 8.59 (m, 2H), 7.67-7.55 (m, 3H), 7.05 (m, 2H), 4.53-4.30 (m, 1H), 4.01 (m, 1H), 3.68 (m, 1H), 1.09 (s, 9H). LC-MS: m/z 365.1 (M+H)+.
henyl-6-(pyridin-4-ylamino)-l,3,5-triazin-2-ylamino)butan-l-ol
Figure imgf000166_0002
1H NMR (METHANOL-d4) δ: 9.38 (m, 2H), 8.54 (m, 2H), 7.65-7.51 (m, 3H), 7.01 (m, 2H), 4.37-4.22 (m, 1H), 3.71 (m, 2H), 1.73 (m, 2H), 1.04 (m, 3H). LC-MS: m/z 337.1 (M+H)+.
enyl-6-(pyridin-4-ylamino)-l,3,5-triazin-2-ylamino)ethanol
Figure imgf000166_0003
1H NMR (METHANOL-d4) δ: 9.40 (m, 2H), 8.56 (m, 2H), 7.65-7.53 (m, 3H), 7.03 (m, 2H), 3.84-3.72 (m, 4H). LC-MS: m/z 309.0 (M+H)+.
Compound 295 - 2-((lS,2R,4R)-bicyclo[2.2 ]heptan-2-yl)-6^henyl-N4-(pyridin-4-yl)-l,3,5-tr z
Figure imgf000166_0004
1H NMR (DMSO-d6) δ: 10.03 (br.s., IH), 8.41-8.31 (m, 4H), 8.03-7.85 (m, 3H), 7.59-7.52 (m, 3H), 4.30-4.10 (m, IH), 2.33-2.09 (m, IH), 2.05-1.90 (m, IH), 1.66-1.19 (m, 8H). LC-MS: m/z 359.2 (M+H)+.
Compound 297 - 2-(3-oxabicyclo[3 ]hexan-6-yl)-6-phenyl-N4-(pyridin-4-yl)-l,3,5-triazine
Figure imgf000167_0001
1H NMR (DMSO-d6) δ: 10.10 (br.s., IH), 8.41-8.38 (m, 4H), 8.32-8.00 (m, IH), 7.95-7.85 (m, 2H), 7.58-7.53 (m, 3H), 3.97 (m, 2H), 3.73 (m, 2H), 2.70-2.55(m, IH), 1.96 (m, 2H). LC-MS: m/z 347.0 (M+H)+.
etan-3-ylmethyl)-6-phenyl-N4-(pyridin-4-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000167_0002
1H NMR (METHANOL-d4) δ: 8.38-8.30 (m, 4H), 7.89 (m, 2H), 7.53-7.44 (m, 3H), 4.83 (m, 2H),
4.56 (m, 2H), 3.83 (m, 2H), 3.35(m, IH). LC-MS: m/z 335.0 (M+H)+.
enyl-6-(pyridin-4-ylamino)-l,3,5-triazin-2-ylamino)cyclohexanol
Figure imgf000167_0003
1H NMR (METHANOL-d4) δ: 8.33-8.44 (m, 4H), 7.90-7.93 (m, 2H), 7.46-7.54 (m, 3H), 3.9-4.2 (m, IH), 3.6-3.8 (m, IH), 2.35-2.38 (m, IH), 1.87-2.06 (m, 3H), 1.26-1.36 (m, 4H). LC-MS: m/z 363.2 (M+H)+.
Compound 305 -
N2-{3-methoxycyclobutyl)-6-p enyl-l^-(pyruiin-4-yl) ,3,5-tr zine-2
Figure imgf000168_0001
1H NMR (METHANOL-d4) δ: 9.32-9.38 (m, 2H), 8.49-8.54 (m, 2H), 7.49-7.62 (m, 3H), 6.98-7.01 (m, 2H), 4.2-4.6 (m, 1H), 3.7-4.1 (m, 1H), 3.3 (br. s., 1H), 2.83-2.84 (m, 1H), 2.47-2.50 (m, 1H), 2.36-2.38 (m, 1H), 2.0-2.04 (m, 1H). LC-MS: m/z 349.2 (M+H)+.
Example 7. Preparation of Compounds of Formula I Wherein R1 and R3 are Taken
Together with the Carbon atom to which they are attached to Form C(=0). The compounds of this Example are prepared by general Scheme 7, Procedure 1 or 2, as set forth below.
Scheme 7
2
Figure imgf000168_0002
H DIEA, DCM Formula I
Example 7, step 3 (Procedure 1): Preparation of N ,6-diphenyl-l,3,5-triazine-2,4-diamine. A mixture of 4-chloro-N,6-diphenyl-l,3,5-triazin-2-amine (4.0 g, 0.14 mol) and NH3.H2O (40 mL) in THF (12 mL) was added in a sealed tube. The reaction mixture was stirred at 80°C for 16 hours. The mixture was extracted with ethyl acetate (50 mLx3). The organic layer was dried over anhydrous Na2S04 and concentrated to give N ,6-diphenyl-l,3,5-triazine-2,4-diamine as a white solid, which was used in the next step directly without further purification.
Preparation of Compound 179 - Isobutyl 4-phenyl-6-(phenyl-amino)-l,3,5-triazin-2-ylcarbamate (Procedure 1, Step 4, reagent 17). Pyridine (60 mg, 0.76 mmol) was added dropwise to a solution of N ,6-diphenyl -l,3,5-triazine-2,4-diamine (100 mg, 0.38 mmol) in DCM (4 mL) under ice-bath cooling. The mixture was then stirred 0°C for 15 min, then isobutyl carbonochloridate (63 mg, 0.46 mmol) was added dropwise and the resultant mixture was stirred at rt for 1 hours. The reaction mixture was concentrated and purified by a standard method to give isobutyl
-phenyl-6-(phenyl-amino)- 1 ,3,5-triazin-2-ylcarbamate.
Figure imgf000169_0001
1H NMR (METHANOL-d4) δ: 8.48 (d, J = 7.2 Hz, 2H), 7.82 (br.s., 2H), 7.55-7.46 (m, 3H), 7.36 (br.s., 2H), 7.07 (br.s., 1H), 4.01 (d, J = 6.8 Hz, 2H), 2.06-2.00 (m, 1H), 1.01 (d, J = 6.8 Hz, 6H). LC-MS: m/z 364.0 (M+H)+
Other compounds of one aspect of the invention were similarly prepared using Example 7,
Procedure 1, step 4 of this example and the appropriate chloridate 17.
Compound 160 - isopropyl 4-phenyl-6-(phenylamino)-l,3,5-triazin-2-ylcarbamate
Figure imgf000169_0002
1H NMR (DMSO-d6) δ: 10.48 (br.s., 1H), 10.12 (br.s., 1H), 8.38 (d, J = 7.2 Hz, 2H), 8.02 (br.s., 2H), 7.61-7.53 (m, 3H), 7.33 (br.s., 2H), 7.04 (t, J = 7.2 Hz, 1H), 4.98 (t, J = 6.4 Hz, 1H), 1.30 (d, J = 6.0 Hz, 6H). LC-MS: m/z 350.1 (M+H)+
(4-phenyl-6-(phenylamino)-l,3,5-triazin-2-yl)pivalamide
Figure imgf000169_0003
1H NMR (DMSO-d6) δ: 10.14 (br.s., 1H), 9.95 (br.s., 1H), 8.40 (d, J = 6.4 Hz, 2H), 8.02 (br.s., 2H), 7.60-7.55 (m, 3H), 7.33 (br.s., 2H), 7.03 (br.s., 1H), 1.27 (s, 9H). LC-MS: m/z 348.0 (M+H)+ Compound 208 - Neopentyl 4-phenyl-6-(phenylamino)-l,3,5-triazin-2-ylcarbamate
Figure imgf000170_0001
1H NMR (DMSO-d6) δ: 10.57 (br.s., 1H), 10.12 (br.s., 1H), 8.38 (d, J = 7.2 Hz, 2H), 8.02 (br.s., 2H), 7.62-7.52 (m, 3H), 7.32 (t, J = 7.2 Hz, 2H), 7.03 (t, J = 7.2 Hz, 1H), 3.85 (s, 2H), 0.96 (s, 9H). LC-MS: m/z 378.0 (M+H)+
Compound 232 - cyclopropylmethyl 4-phenyl-6-(phenylamino)-l,3,5-triazin-2-ylcarbamate
Figure imgf000170_0002
1H NMR (DMSO-d6) δ: 10.46. (br.s., 1H), 10.12 (br.s., 1H), 8.38 (d, J = 7.2 Hz, 2H), 8.02 (br.s. 2H), 7.70-7.54 (m, 3H), 7.31 (br.s., 2H), 7.02 (br.s., 1H), 4.00 (d, J = 7.2 Hz, 2H), 0.88-0.85 (m 1H), 0.56 (d, J = 7.2 Hz, 2H), 0.35 (d, J = 7.2 Hz, 2H). LC-MS: m/z 362.0 (M+H)+
(4-phenyl-6-(phenylamino)-l,3,5-triazin-2-yl)cyclopropanecarboxamide
Figure imgf000170_0003
1H NMR (DMSO-d6) δ: 10.89. (br.s., 1H), 10.13 (br.s., 1H), 8.37 (d, J = 7.2 Hz, 2H), 7.97 (br.s., 2H), 7.62-7.53 (m, 3H), 7.32 (br.s., 2H), 7.04 (t, J = 6.8 Hz, 1H), 2.32 (br.s., 1H), 0.90-0.84 (m., 4H). LC-MS: m/z 332.1 (M+H)+
(4-phenyl-6-(phenylamino)-l,3,5-triazin-2-yl)-lH-pyrazole-5-carboxamide
Figure imgf000170_0004
1H NMR (METHANOL-d4) δ: 8.37 (d, J = 7.2 Hz, 2H), 7.75 (br.s., 2H), 7.72 (s, 1H), 7.51-7.42 (m, 3H), 7.31 (t, J = 7.6 Hz, 2H), 7.03 (t, J = 7.2 Ηζ,ΙΗ), 6.89 (s, 1H). LC-MS: m/z 358.1 (M+H)+ Compound 412 - -hydroxy-N-(4-phenyl-6-(phenylamino)-l,3,5-triazin-2-yl)cyclopropanecarboxamide
Figure imgf000171_0001
1H NMR (METHANOL-d4) δ: 8.36 (d, J = 7.2 Hz, 2H), 7.60-7.89 (m, 2H), 7.48-7.39 (m, 3H), 7.29 (br.s., 2H), 7.25 (br.s., 2H), 1.29 (q, J = 4.8 Hz, 2H), 1.06 (q, J = 4.4 Hz, 2H). LC-MS: m/z 347.9 (M+H)+
Compound 413 - -oxo-N-(4-phenyl-6-(phenylamino)-l,3,5-triazin-2-yl)pyrrolidine-2-carboxamide
Figure imgf000171_0002
H NMR (METHANOL- d ) δ: 8.33 (d, J = 7.6 Hz, 2H), 7.73 (d, J = 8.2 Hz, 2H), 7.53-7.43 (m, 3H), 7.31 (t, J = 7.6 Hz, 2H), 7.03 (t, J = 6.9 Hz, 1H), 4.12-4.08 (m, 1H), 2.44-2.25 (m, 3H), 2.18-2.10 (m, 1H). LC-MS: m/z 375.2 (M+H)+
Compound 415 - -(4-phenyl-6-(phenylamino)-l,3,5-triazin-2-yl)tetrahydrofuran-3-carboxamide
Figure imgf000171_0003
1H NMR (METHANOL-d4) δ: 8.24 (d, J = 7.6 Hz, 2H), 7.55-7.37 (m, 6H), 7.25 (d, J = 7.2 Hz, 2H), 4.13-4.06 (m, 3H), 3.96 (q, J = 8.0 Hz, 1H), 3.36 (q, J = 7.26 Hz, 1H), 2.40-2.20 (m, 2H). LC-MS: m/z 362.2 (M+H)+
Preparation of Compound 414 -lH-Pyrrole-2-carboxylic acid ( 4-phenyl- 6-phenylam in o - [l,3,5]triazin-2-yl)-amide (Procedure 1, step 4 reagent 18). To a solution of (4-amino-6-phenyl-[l,3,5]-triazin-2-yl)-phenyl-amine (210.6 mg, 0.8 mmol) in DCE (4 mL) was added Me3Al (1 mL, 2.0 mmol) at 0°C. The mixture was stirred for 50 mins, warmed up to room temperature and lH-Pyrrole-2-carboxylic acid methyl ester (50 mg, 0.4 mmol) was added. The mixture was stirred for 48hr at 80°C. The reaction mixture was diluted with H20 (5 mL) and extracted with EtOAc (5 mL x 3). The combined organic layers were dried over Na2S04 and concentrated to give a crude residue, which was purified by a standard method to give
-pyrrole-2-carboxylic acid (4-phenyl-6-phenyl-amino-[l,3,5]triazin-2-yl)-amide.
Figure imgf000172_0001
1H NMR (METHANOL-d4) δ: 8.39 (d, J = 7.2 Hz, 1H), 7.75 (br.s., 2H), 7.48-7.40 (m, 3H),7.29 (t, J = 7.2 Hz, 2H), 7.07 (d, J = 2.8 Hz, 1H), 6.99 (s, 2H), 6.18 (t, J = 3.6 Hz, 1H). LC-MS: m/z 357.0
(M+H)+
Other compounds of one aspect of the invention were similarly prepared using Example 7, Procedure 1, step 4 of this example, trimethylaluminum, and the appropriate ester 18.
-oxo-N-(4-phenyl-6-(phenylamino)-l,3,5-triazin-2-yl)propanamide
Figure imgf000172_0002
1H NMR (DMSO-d6) δ: 11.30 (s, 1H), 10.34 (s, 1H), 8.24 (d, J = 6.4 Hz, 2H), 7.82 (d, J = 8.4 Hz, 2H), 7.65-7.50 (m, 3H), 7.38 (br.s., 2H), 7.11 (t, J = 7.2 Hz, 1H), 2.39 (br.s., 3H). LC-MS: m/z 334.2 (M+H)+.
Preparation of Compound 416 - Tert-butyl
4-phenyl-6-(phenylamino)-l,3,5-triazin-2-ylcarbamate Example 7, (Procedure 2). A mixture of 4-chloro-N,6-diphenyl-l,3,5-triazin-2-amine (141mg, 0.5 mmol), tert-butyl carbamate (69.6 mg, 0.6mmol), Pd(AcO)2 (24 mg, 0.05 mmol), X-phos (67.3 mg, 0.1 mmol) and Cs2C03 (326 mg, 1 mmol) in dioxane (5 mL) was purged with N2 for 5 minutes. Then the mixture was heated to 80°C for 2 hours. The reaction mixture was filtered. The filtrate was concentrated and purified by a standard method to give tert-butyl 4-phenyl-6-(phenylamino)-l,3,5-triazin-2-ylcarbamate.
Figure imgf000173_0001
1H NMR (DMSO-d6) δ: 10.24. (br.s., 1H), 10.07 (br.s., 1H), 8.38 (d, J = 6.8 Hz, 2H), 7.99 (br.s., 2H), 7.62-7.53 (m, 3H), 7.31 (br.s., 2H), 7.04 (t, J = 6.8 Hz, 1H), 1.51 (s, 9H). LC-MS: m/z 364.2 (M+H)+.
Other compounds of one aspect of the invention were similarly prepared using Example 7,
Procedure 2 of this example and the appropriate amine 19.
Compound 181 - ethyl 4-phenyl-6-(phenylamino)-l,3,5-triazin-2-ylcarbamate
Figure imgf000173_0002
1H NMR (DMSO-d6) δ: 10.58. (br.s., 1H), 10.12 (br.s., 1H), 8.37 (d, J = 6.8 Hz, 2H), 8.05. (br.s., 2H), 7.60-7.52 (m, 3H), 7.32 (br.s., 2H), 7.04 (t, J = 7.6 Hz, 1H), 4.20 (q, J = 6.8 Hz, 2H), 1.27 (t, J = 6.8 Hz, 1H). LC-MS: m/z 336.2 (M+H)+.
Compound 182 - l,l-dimethyl-3-(4-phenyl-6-(phenylamino)-l,3,5-triazin-2-yl)urea
Figure imgf000173_0003
1H NMR (DMSO-d6) δ: 9.59. (br.s., 1H), 9.35 (br s., 1H), 8.34 (d, J = 7.2 Hz, 2H), 7.86 (d, J = 8.0 Hz, 2H), 7.58-7.51 (m, 3H), 7.31 (t, J = 7.2 Hz, 2H), 7.02 (t, J = 7.2 Hz, 1H), 2.97 (s, 6H).
LC-MS: m/z 335.0 (M+H)+
Compound 207 - l-ethyl-3-(4-phenyl-6-(phenylamino)-l,3,5-triazin-2-yl)urea
Figure imgf000173_0004
1H NMR (DMSO-d6) δ: 10.10. (br.s., 1H), 9.84 (br.s., 1H), 8.30 (d, J = 6.9 Hz, 2H), 7.73 (br.s., 2H), 7.63-7.53 (m, 3H), 7.38 (br.s., 2H), 7.11 (t, J = 7.2 Hz, 1H), 3.33 (br.s., 2H), 1.11 (br.s., 3H). LC-MS: m/z 335.2 (M+H)+
enyl-6-(phenylamino)-l,3,5-triazin-2-yl)propionamide
Figure imgf000174_0001
1H NMR (DMSO-d6) δ: 10.53. (br.s., 1H), 10.10 (br.s., 1H), 8.36 (d, J = 6.9 Hz, 2H), 7.96 (br.s., 2H), 7.62-7.53 (m, 3H), 7.33 (t, J = 7.2 Hz, 2H), 7.04 (t, J = 7.2 Hz, 1H), 2.66-2.62 (m, 2H), 1.08 (t, J = 7.6 Hz, 3H). LC-MS: m/z 320.2 (M+H)+
Compound 243 - -(4-phenyl-6-(phenylamino)-l,3,5-triazin-2-yl)tetrahydrofuran-2-carboxamide
Figure imgf000174_0002
1H NMR (DMSO-d6) δ: 10.21. (br.s., 2H), 8.38 (d, J = 7.6 Hz, 2H), 8.00 (br.s., 2H), 7.63-7.53 (m, 3H), 7.34 (br.s., 2H), 7.06 (t, J = 7.2 Hz, 1H), 4.69 (br.s., 1H), 3.95-3.82 (m., 1H), 4.01-3.97 (m., 1H), 2.32-2.19 (m., 1H), 2.03-1.85 (m., 3H). LC-MS: m/z 362.0 (M+H)+
Compound 244 - 2-isopropoxy-N-(4-phenyl-6-(phenylamino)-l,3,5-triazin-2-yl)acetamide
Figure imgf000174_0003
1H NMR (DMSO-d6) δ: 10.35. (br.s., 1H), 10.20 (br.s., 1H), 8.37 (d, J = 7.2 Hz, 2H), 7.92 (br.s., 2H), 7.62-7.54 (m, 3H), 7.35 (br.s., 2H), 7.08 (t, J = 7.2 Hz, 1H), 4.37 (s, 2H), 3.70-3.67 (m., 1H), 1.15 (d, J = 6.0 Hz, 6H). LC-MS: m/z 364.0 (M+H)+
Compound 324 - 2-hydroxy-N-(4-phenyl-6-(phenylamino)-l,3,5-triazin-2-yl)propanamide
Figure imgf000175_0001
1H NMR (DMSO-d6) δ: 10.28. (br.s., 1H), 10.05. (br.s., 1H), 8.39 (d, J = 7.2 Hz, 2H), 8.09 (br.s., 2H), 7.63-7.55 (m, 3H), 7.36 (br.s., 2H), 7.05 (br.s., 1H), 5.88 (br.s., 1H), 4.38-4.35 (m, 1H), 1.35 (d, J = 6.8 Hz, 3H). LC-MS: m/z 335.9 (M+H)+
Compound 348 - 2-hydroxy-N-(4-phenyl-6-(phenylamino)-l,3,5-triazin-2-yl)acetamide
Figure imgf000175_0002
1H NMR (METHANOL-d4) δ: 8.44 (d, J = 7.6 Hz, 2H), 7.74 (br.s., 2H), 7.60-7.49 (m, 3H), 7.38 (t, J = 7.6 Hz, 2H), 7.12 (t, J = 7.6 Hz, 1H), 4.94 (s, 2H). LC-MS: m/z 322.1 (M+H)+
Additional compounds of Formula I that were prepared according to Example 1, step 3, Procedure C using the appropriate reagent 4 are as follows:
Compound 450 - methyl 4-((4-(isopropylamino)-6-phenyl-l,3,5-triazin-2-yl)amino)picolinate
Figure imgf000175_0003
1H NMR (METHANOL-d4) δ 9.08-8.74 (d, 1 H), 8.49-8.43 (m, 3 H), 8.13-7.83 (m, 1 H), 7.56- 7.48 (m, 3 H), 4.37-4.34 (m, 1 H), 4.02 (s, 3 HO, 1.35-1.30 (m, 6 H). LC-MS: m/z 365.2 (M+H)+ Compound 451 - 2-(4-((4-(isopropylamino)-6-phenyl-l,3,5-triazin-2-yl)amino)pyridin-2- yl)propan-2-ol
Figure imgf000175_0004
1H NMR (METHANOL-d4) δ 8.48-8.23 (m, 4 H), 7.72-7.63 (m, 1 H), 7.56-7.44 (m, 3 H), 4.48-
4.28 (m, 1 H), 1.57 (s, 6 H), 1.30 (d, 6 H). LC-MS: m/z 365.2 (M+H)+
Compound 452 - N2-isopropyl-N4-(4-(methylsulfonyl)phenyl)-6-phenyl-l,3,5-triazine-2,4- diamine
Figure imgf000176_0001
1H NMR (METHANOL-d4) δ 8.41-8.31 (m, 2 H), 7.91-7.88 (m, 4 H), 7.63-7.45 (m, 4 H), 5.51- 5.08 (m, 1 H), 4.48-4.19 (m, 1 H), 3.05 (s, 3 H), 1.30 (d, 6 H). LC-MS: m/z 384.2 (M+H)+
Additional compounds of Formula I were prepared according to Scheme 2 using the appropriate reagents are as follows:
Compound 453 - 6-(3,6-Difluoro-pyridin-2-yl)-N-isopropyl-N'-(3-methanesulfonyl-phenyl)- [l,3,5]triazine-2,4-diamine
Figure imgf000176_0002
1H NMR (METHANOL-d ) δ 8.90-8.40 (m, IH), 8.13-8.11 (m, IH), 7.82-7.80 (m, 2H), 7.71-7.67 (m, IH), 7.59-7.57 (m, IH), 4.42 (m, IH), 3.16 (s, IH), 1.37-1.36 (d, J=6.8 Hz, 6H). LC-MS: m/z 421.2 (M+H)+.
Compound 455 - N-(3,5-Difluoro-phenyl)-N'-isopropyl-6-(4-trifluoromethyl-pyrimidin-2-yl)- [l,3,5]triazine-2,4-diamine
Figure imgf000176_0003
1H NMR (DMSO-d6) δ 10.39-10.42 (m, IH), 9.36-9.38 (m, IH), 8.19-8.34 (m, 2H), 7.68-7.71 (m, 2H), 6.79-6.84 (m, IH), 4.10-4.15 (m, IH), 1.18-1.23 (m, 6H). LC-MS: m/z 412.3 (M+H)+. Compound 456 - N-(5-Fluoro-pyridin-3-yl)-6-(3-fluoro-pyridin-2-yl)-N'-isopropyl- [l,3,5]triazine-2,4-diamine
Figure imgf000177_0001
1H NMR (METHANOL-d4) δ 8.70 (s, IH), 8.61-8.40 (m, IH), 8.15-8.10 (m, 2H), 7.87-7.83 (m, IH), 7.71-7.67 (m, IH), 4.31-4.27 (m, IH), 1.35-1.27 (m, 6H). LC-MS: m/z 344.2 (M+H)+. Compound 458 - 6-(4-Amino-pyrimidin-2-yl)-N-(3,5-difluoro-phenyl)-N'-isopropyl- [l,3,5]triazine-2,4-diamine
Figure imgf000177_0002
1H NMR (METHANOL-d4) δ (s, IH), 7.50-7.52 (d, J = 8.8 Hz, 2H), 6.58-6.67 (m, 2H), 4.23-4.55 (m, IH), 1.25-1.34 (m, 6H). LC-MS : m/z 359.0 (M+H)+.
Compound 459 - N-(3,5-Difluoro-phenyl)-6-(3-fluoro-pyridin-2-yl)-N'-isopropyl-[l,3,5]triazine- 2,4-diamine
Figure imgf000177_0003
1H NMR (METHANOL-d4) δ 8.54-8.53 (d, IH), 7.82-7.78 (m, IH), 7.66-7.61 (m, IH), 7.55-7.50
(m, 2H), 6.60-6.53 (m, IH), 4.39-4.24 (m, IH), 1.34-1.23 (m, 6H). LC-MS: m/z 361.2 (M+H)+.
Compound 460 - N-(3,5-Difluoro-phenyl)-6-(3,6-difluoro-pyridin-2-yl)-N'-isopropyl-
[l,3,5]triazine-2,4-diamine
Figure imgf000177_0004
1H NMR (METHANOL-d ) δ 8.03-7.97 (m, IH), 7.51-7.49 (m, 2H), 7.41-7.30 (m, IH), 6.68-6.64 (m, IH), 4.31-4.24 (m, IH), 1.35-1.27 (m, 6H). LC-MS: m/z 379.1 (M+H)+.
Compound 461 - N-(3,5-Difluoro-phenyl)-6-(3-fluoro-6-methoxy-pyridin-2-yl)-N'-isopropyl-
[l,3,5]triazine-2,4-diamine
Figure imgf000178_0001
1H NMR (METHANOL-d4) δ 7.83-7.79 (m, IH), 7.54-7.51 (m, 2H), 7.22-7.19 (m, IH), 6.78 (m, IH), 4.35-4.31 (m, IH), 4.08 (s, 3H), 1.39-1.31 (m, 6H). LC-MS: m/z 391.3 (M+H)+.
Compound 462 - 6-(6-Ami -pyridin-2-yl)-N-(6-fluoro-pyridin-3-yl)-N'-isopropyl-
[l,3,5]triazine-2,4-diamine
Figure imgf000178_0002
1H NMR (METHANOL-d4) δ 8.65-8.58 (m, IH), 8.50-8.30 (m, IH), 8.20-7.61 (m, 2H), 7.
(m, 2H), 4.60-4.20 (m, IH), 1.30 (d, 6H). LC-MS: m/z 340.9 (M+H)+.
Compound 463 - N-(3,5-Difluoro-phenyl)-N'-isopropyl-6-(6-prop-l-ynyl-pyridin-2-yl)-
[l,3,5]triazine-2,4-diamine
Figure imgf000178_0003
1H NMR (METHANOL-d4) δ 8.39-8.34 (m, IH), 7.94-7.90 (t, IH), 7.60-7.52 (m, 3H), 6.62-6.57 (m, IH), 4.50-4.24 (m, IH), 2.12 (s, 3H), 1.34-1.29 (m, 6H). LC-MS: m/z 380.9 (M+H)+.
Compound 464 - N-(3,5-Difluoro-phenyl)-N'-isopropyl-6-(6-methylamino-pyridin-2-yl)- [l,3,5]triazine-2,4-diamine
Figure imgf000179_0001
1H NMR (METHANOL-d4) δ 7.72-7.67 (m, IH), 7.63-7.52 (m, 3H), 6.68-6.65 (d, IH), 6.60-6.56 (m, 1H),4.36-4.16 (m, 2H), 2.98 (s, 3H). LC-MS: m/z 441.9 (M+H)+.
Compound 465 - N-(3,5-Difluoro-phenyl)-6-(6-methylamino-pyridin-2-yl)-N'-(2,2,2-trifluoro- ethyl)-[l,3,5]triazine-2,4-diamine
Figure imgf000179_0002
1H NMR (METHANOL-d4) δ 8.00-7.85 (m, IH), 7.84-7.78 (m, IH), 7.50-7.45 (m, IH), 7.19-7.17 (m, IH), 6.68-6.60 (m, IH), 4.26-4.23 (m, IH), 3.14-3.12(d, 3H), 1.33- 1.28 (m, 6H). LC-MS: m/z 372.3 (M+H)+.
Compound 466 - 6-(2,6-difluorophenyl)-N2-isopropyl-N4-(3-(methylsulfonyl)phenyl)-l,3,5- triazine-2,4-diamine
Figure imgf000179_0003
1H NMR (METHANOL-d ) : δ 9.0-8.4 (m, l.OH), 8.05-7.75 (m, IH), 7.75-7.4 (m, 3 H), 7.15-7.05 (m, 2H), 4.45-4.1 (m, IH), 3.15 (s, 3H), 1.3 (d, J=6.4, 6H).
LC-MS : m/z 419.8 (M+H)+.
Compound 467 - N-(3-Fluoro-phenyl)-N'-isopropyl-6-(6-prop-l-ynyl-pyridin-2-yl)- [l,3,5]triazine-2,4-diamine
Figure imgf000179_0004
1H NMR (METHANOL-d4) δ 8.33-8.31 (m, IH), 7.92-7.82 (m, 2H), 7.58-7.56 (m, IH), 7.40-7.30 (m, 2H), 6.78-6.76 (m, IH), 4.25-4.22 (m, IH), 2.10 (s, 3H), 1.33-1.28 (m, 6H). LC-MS: m/z 363.2 (M+H)+.
Compound 468 - 6-(6-Amino-pyridin-2-yl)-N-isopropyl-N'-(5-trifluoromethyl-pyridin-3-yl)- [l,3,5]triazine-2,4-diamine
Figure imgf000180_0001
1H NMR (METHANOL-d4) δ 9.21 (s, 2H), 8.48 (s, IH), 7.70-7.58 (m, 2H), 6.74-6.72 (m, IH),
4.22 (m, IH), 1.31-1.29 (d, J=8.0 Hz, 6H). LC-MS: m/z 391.3 (M+H)+.
Compound 469 - 6-[4-(3,5-Difluoro-phenylamino)-6-isopropylamino-[l,3,5]triazin-2-yl]-5- fluoro-pyridin-2-ol
Figure imgf000180_0002
1H NMR (METHANOL-d ) δ 7.71-7.65 (m, 2H), 7.49-7.47 (m, 2H), 6.77-6.72 (m, IH), 6.55- 6.53(m, IH), 4.40-4.18 (m, IH), 1.30-1.25 (m, 6H). LC-MS: m/z 377.2 (M+H)+.
Compound 470 - 6-(6-Amino-pyridin-2-yl)-N-(5-fluoro-pyridin-3-yl)-N'-isopropyl- [l,3,5]triazine-2,4-diamine
Figure imgf000180_0003
1H NMR (METHANOL-d4) δ 9.38-9.35 (m, IH), 8.77-8.63 (m, 2H), 8.09-7.86 (m, 2H), 7.25-7.22 (m, IH), 4.28-4.25 (m, IH), 1.34 (dd, 6H). LC-MS: m/z 341.1 (M+H)+.
Compound 471 - N-(3-Fluoro-phenyl)-N'-isopropyl-6-(2-methyl-oxazol-4-yl)-[l,3,5]triazine-2,4- diamine
Figure imgf000181_0001
1H NMR (METHANOL-d4) δ 8.46-8.43 (m, IH), 7.85-7.82 (m, IH), 7.40-7.27 (m, 2H), 6.78-6.74 (m, IH), 4.25-4.22 (m, IH), 2.57 (s, H), 1.29 (dd, J= 13.2 Hz, 6.4 Hz, 6H). LC-MS : m/z 329.2 (M+H)+.
Compound 472 - N-(3-Fluoro-phenyl)-N'-isopropyl-6-(5-methyl-isoxazol-3-yl)-[l,3,5]triazine- -diamine
Figure imgf000181_0002
1H NMR (METHANOL-d ) δ 7.87-7.82 (m, IH), 7.41-7.38 (m, IH), 7.34-7.26 (m, IH), 6.77-6.68 (m, 2H), 4.38-4.21 (m, IH), 2.53 (s, H), 1.29 (dd, J = 10.8 Hz, 6.8 Hz, 6H). LC-MS: m/z 329.3 (M+H)+.
Compound 473 - 6-(2,6-Difluoro-phenyl)-N-(3-fluoro-phenyl)-N'-isopropyl-[l,3,5]triazine-2,4- diamine
Figure imgf000181_0003
1H NMR (METHANOL-d ) δ 6.98-6.97 (m, IH), 6.69-6.54 (m, 3H), 6.28-6.23 (m, 2H), 5.92 (m, IH), 3.47-3.44 (m, IH), 0.49 (d, 6H). LC-MS: m/z 359 (M+H)+.
Compound 474 - 6-(2,6-Difluoro-phenyl)-N-(5-fluoro-pyridin-3-yl)-N'-isopropyl-[l,3,5]triazine- 2,4-diamine
Figure imgf000181_0004
1H NMR (METHANOL-d4) δ 9.23-9.01 (m, IH), 8.78-8.43 (m, 2H), 7.63-7.61 (m, IH), 7.
(m, 2H), 4.31-4.20 (m, IH), 1.33 (d, 6H). LC-MS: m/z 361.1 (M+H)+.
Compound 475 - N-(3-Fluoro-phenyl)-N'-isopropyl-6-(4-trifluoromethyl-thiazol-2-yl)-
[l,3,5]triazine-2,4-diamine
Figure imgf000182_0001
1H NMR (METHANOL-d ) δ 8.71 (s, IH), 8.24 (d, J = 7.6 Hz, IH), 8.00-7.86 (m, IH), 7.52-7.50 (m, IH), 7.36-7.27 (m, IH), 4.25-4.08 (m, IH), 1.21 (d, J = 6.4 Hz, 6H). LC-MS: m/z 399.0 (M+H)+.
Compound 476 - N-(3,5-Difluoro-phenyl)-N'-isopropyl-6-(2-methyl-oxazol-4-yl)-[l,3,5]triazine- -diamine
Figure imgf000182_0002
1H NMR (METHANOL-d4) δ 8.67 (br, IH), 7.42 (d, J = 9.2 Hz, 2H), 6.77-6.72 (m, IH), 4.28-4.23
(m, IH), 2.56 (s, 3H), 1.28 (d, J = 9.6 Hz, 6H). LC-MS : m/z 347.1(M+H)+.
Compound 477 - 6-(6-amino-3-fluoropyridin-2-yl)-N2-(3,5-difluorophenyl)-N4-isopropyl-l,3,5- triazine-2,4-diamine
Figure imgf000182_0003
1H NMR (METHANOL- d4) δ 7.55-7.45 (m, 2H), 7.45-7.35 (m, IH), 7.0-6.9 (m, IH), 6.65-6.5 (m, IH), 4.4-4.15 (m, IH), 1.4-1.25 (m, 6H). LC-MS: m/z 376.2 (M+H)+.
Compound 478 - 6-(4-Amino-pyrimidin-2-yl)-N-cyclopropylmethyl-N'-(3,5-difluoro-phenyl)- [l,3,5]triazine-2,4-diamine
Figure imgf000183_0001
1H NMR (METHANOL-d4) δ 8.26-8.25 (d, J = 5.6 Hz, IH), 7.532-7.490 (m, 2H), 6.66-6.57 (m, 2H), 3.43-3.23 (m, 2H), 1.16-1.18 (m, IH), 0.58-0.51 (m, 2H), 0.34-0.29 (m, 2H). LC-MS: m/z 371.2 (M+H)+.
Compound 479 - 6-(4-Amino-pyrimidin-2-yl)-N-tert-butyl-N'-(3,5-difluoro-phenyl)- [l,3,5]triazine-2,4-diamine
Figure imgf000183_0002
1H NMR (METHANOL-d ) δ 8.28-8.26 (d, J = 5.2 Hz, 1Η),7.49-7.47 (d, J = 8 Hz, 2H), 6.66-6.60 (m, 2H), 1.54 (s, 9H). LC-MS: m/z 373.2 (M+H)+.
Compound 480 - 6-(4-Amino-pyrimidin-2-yl)-N-(3,5-difluoro-phenyl)-N'-(2,2,2-trifluoro-ethyl)- [l,3,5]triazine-2,4-diamine
Figure imgf000183_0003
1H NMR (METHANOL- d ) δ 8.29-8.26 (m, 1 H), 7.55-7.44 (m, 2H), 6.67-6.59 (m, 2H), 4.44-4.20 (m, 2H). LC-MS: m/z 399.2 (M+H)+.
Compound 481 - 6-(4-amino-6-(trifluoromethyl)pyrimidin-2-yl)-N2-(3,5-difluorophenyl)-N4- isopropyl-l,3,5-triazine-2,4-diamine
Figure imgf000183_0004
1H NMR (METHANOL-d4) δ 7.53 (d, J = 8.0 Hz, 2 H), 6.98 (s, IH), 6.63-6.55 (m, IH), 4.50-4.23 (m, IH), 1.34 (d, J = 6.2 Hz, 6 H). LC-MS: m/z 427.1 (M+H)+. Compound 482 - 6-(2-Amino-pyrimidin-4-yl)-N-(3,5-difluoro-phenyl)-N'-isopropyl- [l,3,5]triazine-2,4-diamine
Figure imgf000184_0001
1H NMR (METHANOL-d4) δ 8.47-8.46 (m, IH), 7.60-7.48 (m, 3H), 4.26-4.22 (m, IH), 1.33-1.26 (m, 6H). LC-MS: m/z 372.3 (M+H)+.
Compound 483 - 6-(4,6-dichloropyridin-2-yl)-N2-isopropyl-N4-(3-(methylsulfonyl)phenyl)-l,3,5- triazine-2,4-diamine
Figure imgf000184_0002
1H NMR (DMSO-d6) δ 10.40 (br, IH), 8.88 (s, IH), 8.34-8.18 (m, 2 H), 7.99 (s, IH), 7.81-7.79 (m, IH), 7.56-7.53 (m, 2H), 4.23 (br, IH), 3.18 (m, 3H), 1.20 (s, 6H). LC-MS: m/z 475.0 (M+H)+. Compound 484 - 6-(3-fluoro-6-(trifluoromethyl)pyridin-2-yl)-N2-isopropyl-N4-(3- (methylsulfonyl)phenyl)-l,3,5-triazine-2,4-diamine
Figure imgf000184_0003
1H NMR (METHANOL-d4) δ 8.52 (s, IH), 8.03-7.95 (m, 2H), 7.79 (br, IH), 7.61-7.53 (m, 2H),
4.36-4.28 (m, IH), 3.11 (d, 3H), 1.31-1.21 (m, 6H). LC-MS: m/z 471.1 (M+H)+.
Compound 485 - 6-(6-amino-4-chloropyridin-2-yl)-N2-(3,5-difluorophenyl)-N4-isopropyl-l,3,5- triazine-2,4-diamine
Figure imgf000184_0004
1H NMR (METHANOL-d4) δ 7.66 (s, IH), 7.49-7.47 (d, 2H), 6.73 (s, IH), 6.57-6.50 (m, IH), 4.47-4.09 (m, IH), 1.35-1.26 (m, 6H). LC-MS: m/z 392.1 (M+H)+.
Compound 486 - 6-(4-chloro-6-methoxypyridin-2-yl)-N2-(3,5-difluorophenyl)-N4-isopropyl- -triazine-2,4-diamine
Figure imgf000185_0001
1H NMR (METHANOL-d4) δ 8.05 (s, IH), 7.52 (br, 2H), 7.00 (s, IH), 6.58-6.52 (m, IH), 4.40-
4.21 (m, IH), 4.07 (s, 3H), 1.31-1.29 (d, 6H). LC-MS: m/z 407.1 (M+H)+.
Compound 487 - ( 2-( 4-( ( 3,5-difluorophenyl)amino )-6-( isopropylamino )-l,3,5-triazin-2-yl)-6-
(trifluoromethyl)pyridin-4-yl)methanol
Figure imgf000185_0002
1H NMR (METHANOL-d4) δ 8.66 (s, IH), 7.92 (s, IH), 7.54-7.52 (d, J = 8 Hz, 2H), 6.60-6.54 (m, IH), 4.83 (s, 2H), 4.47-4.22 (m, IH), 1.33-1.31 (d, J = 6.4 Hz, 6H). LC-MS: m/z 441.1 (M+H)+. Compound 488 - 6-(6-(l,l-difluoroethyl)-4-fluoropyridin-2-yl)-N2-isopropyl-N4-(3- (methylsulfonyl)phenyl)-l,3,5-triazine-2,4-diamine
Figure imgf000185_0003
1H NMR (METHANOL-d ) δ 8.95 (m, IH), 8.3(m, IH), 7.75(m, IH), 7.6-7.5 (m, 3H), 4.4 (m, IH), 3.15 (s, 3H), 2.2-2.0 (m, 3H), 1.4-1.3 (m, 6H).
Compound 489 - 6-(6-amino-4-fluoropyridin-2-yl)-N2-(3,5-difluorophenyl)-N4-isopropyl-l,3,5- triazine-2,4-diamine
Figure imgf000186_0001
1H NMR (DMSO) δ 10.15 (m, IH), 8.0 (m, IH), 7.7-7.5(m, 2H), 7.2 (m, IH), 6.75 (m, IH) 6.36 (m, IH), 6.26 (m, 2H), 4.4-4.0 (m, IH), 1.2 (m, 6H).
Compound 490 - ( 2-chloro-6-( 4-(( 3,5-difluorophenyl)amino )-6-( isopropylamino )-l,3,5-triazin-2- yl)pyridin-4-yl)methanol
Figure imgf000186_0002
1H NMR (METHANOL-d4) δ 10.28-10.24 (m, IH), 8.29 (s, IH), 8.16-7.88 (m, IH), 7.71-7.54 (m, 2H), 7.54-7.53 (d, IH), 6.80-6.72 (m, IH), 5.63-5.60 (q, 2H), 4.63-4.61 (m, IH), 4.33-4.05 (m, IH), 1.21-1.19 (d, 6H). LC-MS : m/z 407.1 (M+H)+.
Compound 491 - 6-(6-aminopyridin-2-yl)-N2-(3,5-difluorophenyl)-N4-(2,2,2-trifluoroethyl)- l,3,5-triazine-2,4-diamine
Figure imgf000186_0003
1H NMR (METHANOL-d4) δ 8.10-8.07 (m, 1 H), 7.93-7.86 (m, 1 H), 7.54-7.41 (m, 2 H), 7.25- 7.22 (m, 1 H), 6.69-6.65 (m, 1 H), 4.42-4.25 (m, 2 H). LC-MS : m/z 398.2 (M+H)+.
Compound 492 - 6-( 6-aminopyridin-2-yl)-N2-(3-fluorophenyl)-N4-isopropyl-l,3,5-triazine-2,4- diamine
Figure imgf000186_0004
1H NMR (METHANOL-d ) δ 8.04-8.00 (m, 1 H), 7.83 (br, 2 H), 7.40-7.37 (m, 1 H), 7.33-7.28 (m,
1 H), 7.18-7.16 (m, 1 H), 6.79 (t, 1 H), 4.51-4.25 (m, 1 H), 1.29 (d, 6 H). LC-MS : m/z 340.2 (M+H)+.
Compound 493 - 6-(6-amino-3-fluoropyridin-2-yl)-N2-(tert-butyl)-N4-(2- ( trifluoromethyl)pyridin-4-yl)-l,3,5- triazine-2,4-diamine
Step 1: Preparation of (E)-2-(tert-butyl)-l-(diaminomethylene)guanidine. To a mixture of 1- phenyl-2-cyanoguanidine (10 g, 0.119 mol) in ethanol/water (176.5 mL/70.6 mL) was added CuS045H20 (14.9 g, 0.059 mol), followed by 2-methylpropan-2-amine (11.3 g, 0.155 mol). The mixture was heated to reflux for 16 hours. To the mixture was added water (137 mL) and aq.HCl (59.5 mL in 100 mL of water) at 25-30°C. The resultant mixture was stirred at r.t. for 30 min. Then Na2S (47.6 g in 100 mL of water) was added and stirred for another 30 min. The insoluble CuS was filtered off. The filtrate was cooled to 10°C and added aqueous NaOH (27 g NaOH in 100 mL water) dropwise. The mixture was extracted with dichloromethane (100 mLx3). The aqueous layer was concentrated and the residue was added dichloromethane (200 mL) and the mixture was stirred for 1 hour and the mixture was filtrated. The filtrated was concentrated to give (E)-2-(tert-butyl)-l-(diaminomethylene)guanidine as a brown solid.
Figure imgf000187_0001
1H NMR (CDC13) δ 1.32-1.37 (m, 9H).
Step 2: Preparation of N2-(tert-butyl)-6-(3,6-difluoropyridin-2-yl)-l,3,5 riazine-2,4-diamine.
The mixture of (E)-2-(tert-butyl)-l-(diaminomethylene) guanidine (1.2 g, 7.6 mmol), methyl 3,6- difluoropicolinate (1.3 g, 7.6 mol) and MeONa (0.9 g, 15.2 mol) in MeOH (25 mL) was stirred for 5 hours at r.t. TLC showed the reaction was completed. The mixture was poured into water (15 mL), extracted with EA (50 mL) for 3 times. The combine organic layer was dried, concentrated and purified by Prep-HPLC to give N2-(tert-butyl)-6-(3,6-difluoropyridin-2-yl)-l,3,5-triazine-2,4- diamine as a white solid.
Figure imgf000187_0002
1H NMR (CDCI3) δ 7.5 (m, 1H), 7.0 (m, 1H), 5.4(B, 1H), 5.1-5.2 (br s, 2H), 4.4 (m, 9H). Step 3: Preparation of N -(tert-butyl)-6-(3,6-difluoropyridin-2-yl)-N4-(2-(trifluoromethyl) pyridin-4-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000188_0001
To the mixture of N -(tert-butyl)-6-(3,6-difluoropyridin-2-yl)-l,3,5-triazine-2,4-diamine ( 0.4 g, 1.4 mmol) , 4-chloro-2-(trifluoromethyl)pyridine (0.31 g, 1.7 mmol) , Cs2C03 (0.7 g, 2.1 mmol) and X-phos (0.048 g, 0.07 mmol) in dioxane (10 mL) was added Pd(OAc)2 under N2 protection. The reaction mixture was heated to 80 deg and stirred for 2 hours. TLC showed the reaction was completed, the reaction mixture was added water (10 mL), extracted with EA (100 mL) for 3 times. The combine organic layer was dried and concentrated. The residue was purified by a
2 4
standard method to give N -(tert-butyl)-6-(3,6-difluoropyridin-2-yl)-N -(2- -4-yl)- 1 ,3,5- triazine-2,4-diamine.
Figure imgf000188_0002
1H NMR (CDC13) δ 8.6-8.4 (m, 2H), 7.65 (m, 1H) , 7.5-7.4 (m, 2H) , 7.1 (m, 1H) , 5.7 (m, 1H), 1.45 (m, 9H).
Step 4: Preparation of 6-(6-amino-3-fluoropyridin-2-yl)-N2-(tert-butyl)-N4-(2-(trifluoromethyl) pyridin-4-yl)-l,3,5- triazine-2,4-diamine - Compound 494
Figure imgf000188_0003
2 4
To the solution of N -(tert-butyl)-6-(3,6-difluoropyridin-2-yl)-N -(2-(trifluoromethyl)pyridine-4- yl)-l,3,5-triazine-2,4-diamine (300 mg, 0.7 mmol) and Cul (134 mg, 0.7mmol) in THF (5 mL) was added sat.NHs/EtOH (15 mL) solution. The reaction mixture was stirred in a seal reactor at 130 deg for 10 hours. LCMS showed the reaction was completed. The solvent was removed and the residue was purified by a standard method to give 6-(6-amino-3-fluoropyridin-2-yl)-N -(tert- methyl)pyridin-4-yl)-l,3,5-triazine-2,4-diamine.
Figure imgf000189_0001
1H NMR (CDC13) δ 8.63 (m, 1H), 8.45 (m, 1H), 7.85 (m, 1H), 7.5-7.4(m, 1H), 6.75 (m, 1H), 1.5 (m, 9H).
According to the general strategy outlined in Scheme 3, step 2, the following intermediates were prepared:
-( 4-( trifluoromethyl)pyrimidin-2-yl)-l,3,5-triazine-2,4( lH,3H)-dione
Figure imgf000189_0002
LCMS: m/z 260.1 (M+H)+.
Methyl 6-(4,6-dioxo-l,4,5,6-tetrahydro-l,3,5-triazin-2-yl)pyridin-2-ylcarbamate
Figure imgf000189_0003
LCMS: m/z 264.2 (M+H)+.
6-(4-methoxypyridin-2-yl)-l,3,5-triazine-2,4(lH,3H)-dione
Figure imgf000190_0001
LCMS: m/z 221.1 (M+H)+.
According to the general strategy outlined in Scheme 3, step 3, the following intermediates were prepared:
2,4-dichloro-6-(4-(trifluoromethyl)-pyrimidin-2-yl)-l,3,5-triazine.
Figure imgf000190_0002
LCMS: m/z 296.0 (M+H)+.
2,4-Dichloro-6-(6-difluoromethyl -pyridin-2-yl)-[l,3,5]triazine
Figure imgf000190_0003
LCMS: m/z 277.0 (M+H)+.
2,4-Dichloro-6-[6-(l,l-difluoroethyl)-pyridin-2-yl]-[l,3,5]triazine
Figure imgf000190_0004
LCMS: m/z 290.9 (M+H)+.
Methyl 6-(4,6-dichloro-l,3,5-triazin-2-yl)-pyridin-2-ylcarbamate
Figure imgf000191_0001
-Dichloro-6-(4-methoxypyridin-2-yl)-l,3,5-triazine
Figure imgf000191_0002
LCMS: m/z 257.1 (M+H)+.
According to the general strategy outlined in Scheme 3, steps 4-5, the following compounds were prepared from appropriate reagents and intermediates:
Compound 494 - N-[2-(l, l-Difluoro-ethyl)-pyridin-4-yl]-N'-isopropyl-6-(6-trifluoromethyl- pyridin-2-yl)-[l,3,5] triazine-2,4-diamine
Figure imgf000191_0003
1H NMR (METHANOL-d4) δ 8.67 (s, 1H), 8.51-8.18 (m, 3H), 7.97-7.73 (m, 2H), 4.51-4.32 (m, 1H), 1.97 (t, J = 18.8 Hz, 2H), 1.32 (d, J = 6.4 Hz, 6 H). LC-MS: m/z 440.3 (M+H)+.
Compound 495 - 3-[4-(6-Chloro-pyridin-2-yl)-6-(2-trifluoromethyl-pyridin-4-ylamino)- [l,3,5]triazin-2-ylamino]-2,2-dimethyl-propan-l-ol
Figure imgf000191_0004
1H NMR (METHANOL-d4) δ 8.63-8.45 (m, 3H), 8.44-7.99 (m, 2H), 7.97-7.62 (m, IH), 3.49 (s, IH), 3.43 (s., IH), 3.40 (s, IH), 3.23 (s., IH), 0.98 (d., J = 6.4 Hz, 6H). LC-MS: m/z 454.3 (M+H)
+
Compound 496 - 2-{4-[4-Isopropylamino-6-(6-trifluoromethyl-pyridin-2-yl)-[l,3,5]triazin-2- ylamino]-pyridin-2-yl}-propan-2-ol
Figure imgf000192_0001
1H NMR (METHANOL-d ) δ 8.66 (s, IH), 8.29-8.11 (m, 3H), 7.88 (s, IH), 7.58-7.56 (m, IH), 4.40-4.29 (m., IH), 1.49 (s, 6H), 1.25 (d., J=6.4 Hz, 6H). LC-MS: m/z 434.3 (M+H)+.
Compound 497 - 3-[4-(6-Chloro-pyridin-2-yl)-6-isopropylamino-[l,3,5]triazin-2-ylamino]-N- cyclopropylmethyl-benzenesulfonamide
Figure imgf000192_0002
1H NMR (METHANOL-d4) δ 8.70 (s, IH), 8.50 (m, IH), 8.14-8.10 (m, IH), 7.82-7.80 (m, IH), 7.69-7.67 (m., 2H), 7.58 (m, IH), 4.42 (m, IH), 2.78-2.76 (d., J = 6.8 Hz, 2H), 1.36- 1.28 (d, J = 10 Hz, 6H), 0.87-0.81 (m, IH), 0.43-0.38 (m, 2H), 0.10-0.07 (m, 2H). LC-MS: m/z 474.3 (M+H)+. Compound 498 - 5-[4-(6-Chloro-pyridin-2-yl)-6-(2,2-dimethyl-propylamino)-[l,3,5]triazin-2- ylamino ]-nicotinonitrile
Figure imgf000192_0003
IH NMR (METHANOL-d ) δ 9.01-8.94 (m, 2H), 8.53-8.41 (m, 2H), 8.00-7.96 (m, IH), 7.62-7.60 (m, IH), 3.35 (s, 3H), 1.00 (s, 9 H). LC-MS : m/z 395.2 (M+H)+.
Compound 499 - 6-(6-Chloro-pyridin-2-yl)-N-(2-methoxy-l-methyl-ethyl)-N'-(2-trifluoromethyl- pyridin-4-yl)-[l,3,5]triazine-2,4-diamine
Figure imgf000193_0001
1H NMR (METHANOL-d4) δ 8.62-8.43 (m, 3H), 8.25-8.61 (m, 3H), 4.40-4.36 (m, 1H), 3.56-3.48
(m, 2H), 3.47 (s, 3H), 1.32-1.26 (s, 3 H). LC-MS : m/z 440.3 (M+H)+.
Compound 500 - l-[4-(2-Fluoro-pyridin-4-ylamino)-6-(6-trifluoromethyl-pyridin-2-yl)-
[l,3,5]triazin-2-ylamino]-2-methyl-propan-2-ol
Using the standard procedure described above except replacing t-BuONa by CS2CO3 yielded the title compound.
Figure imgf000193_0002
1H NMR (METHANOL-d ) δ 8.79-8.81 (d, J = 8 Hz, 1H), 8.37-8.43 (m, 1H), 8.20-8.24 (m, 2H),
7.56-7.72 (m, 2H), 3.65 (s, 2H), 1.36 (s, 6H). LC-MS : m/z 424.2 (M+H)+.
Compound 501 - N-Isopropyl-N'-(6-methyl-pyridazin-4-yl)-6-(6-trifluoromethyl-pyridin-2-yl)-
[l,3,5]triazine-2,4-diamine
Using the standard procedure described above except replacing t-BuONa by CS2CO3 yielded the title compound.
Figure imgf000193_0003
1H NMR (METHANOL-d ) δ 9.30-8.85 (m, 2 H), 8.78-8.80 (d, J = 8 Hz, 1H), 8.29-8.28 (m, 8.07-8.15 (m, 1H), 4.36-4.55 (m, 1H), 2.87 (s, 3H), 1.38-1.41 (m, 6H). LC-MS: m/z 391.2 (M+H)+.
Compound 502 - 4-[4-(6-Chloro-pyridin-2-yl)-6-(2-trifluoromethyl-pyridin-4-ylamino)- [l,3,5]triazin-2-ylamino]-piperidine-l-carboxylic acid tert-butyl ester
Figure imgf000194_0001
1H NMR (CDC13-d6) δ 8.51-8.55 (m, 2H), 8.27 (d, J = 7.6 Hz, IH), 7.77 (t, J = 8 Hz, IH), 7.45-
7.50 (m, 2H), 7.28-7.33 (m., IH), 5.65 (d, J = 7.6 Hz, IH), 3.95-4.11 (m, 3H), 2.88-2.93 (m., 2H),
2.02 (d, J = 11.2 Hz, 2H), 1.41-1.51 (m, 11 H). LC-MS : m/z 552.0 (M+H)+.
Compound 503 - N-(5-Fluoro-pyridin-3-yl)-N'-isopropyl-6-(6-trifluoromethyl-pyridin-2-yl)-
[l,3,5]triazine-2,4-diamine
Figure imgf000194_0002
1H NMR (METHANOL-d4) δ 8.66-8.62 (m, 2H), 8.54 (br, IH), 8.17 (t, J = 7.8 Hz, IH), 8.09-8.05 (m, IH), 7.93 (d, J = 7.6 Hz, IH), 4.24-4.21 (m, IH), 1.26 (d, J = 4.2 Hz, 6H). LC-MS: m/z 394.2 (M+H)+.
N-(6-Fluoro-pyridin-3-yl)-N' sopropyl-6-(6-trifluoromethyl-pyridin-2-yl)-[l,3,5]tr ^ diamine
Figure imgf000194_0003
1H NMR (METHANOL-d4) δ 8.53-8.50 (m, 2H), 8.46-8.24 (m, IH), 8.07 (t, J = 7.8 Hz, IH), 7.84 (d, J = 7.6 Hz, IH), 6.97-6.94 (m, IH), 4.35-4.13 (m, IH), 1.19 (d, J = 6.4 Hz, 6H). LC-MS: m/z 394.1 (M+H)+.
Compound 504 - N-(3-Oxa-bicyclo[3.1.0]hex-6-yl)-N'-(2-trifluoromethyl-pyridin-4-yl)-6-(6- trifluoromethyl-pyridin-2-yl)-[l,3,5]triazine-2,4-diamine
Figure imgf000194_0004
1H NMR (METHANOL-d4) δ 8.60 (dd, J = 8.0 Hz, 2.0, 1H) 8.53 (dd, J = 5.6 Hz, 1.6, 1H), 8.34 (s, 1H), 8.26-8.21 (m, 2H), 8.01-7.97 (m, 1H), 4.10 (d, J = 7.4 Hz, 2H), 3.80 (d, J = 8.4 Hz, 2H), 2.80- 2.77 (m, 1H), 2.06 (s, 2H). LC-MS : m/z 484.3 (M+H)+.
Compound 505 - 4-[4-(3-Oxa-bicyclo[3.1.0]hex-6-ylamino)-6-(6-trifluoromethyl-pyridin-2-yl)- [l,3,5]triazin-2-ylamino]-pyridine-2-carbonitrile
Using the standard procedure described above except replacing t-BuONa by CS2CO3 to yield the title compound.
Figure imgf000195_0001
1H NMR (METHANOL-d ) δ 8.69-8.51 (m, 3H), 8.24-8.20 (m, 1H), 8.09-7.98 (m, 2H), 4.12 (d, J = 9.2 Hz, 2H), 3.84 (d, J = 8.4 Hz, 2H). 2.75 (s, 1H), 2.02 (s, 2H). LC-MS: m/z 441.3 (M+H)+. Compound 506 - N-(6-Fluoro-pyridin-3-yl)-N'-(3-oxa-bicyclo[3.1.0]hex-6-yl)-6-(6- trifluoromethyl-pyridin-2-yl)-[l,3,5]triazine-2,4-diamine
Figure imgf000195_0002
1H NMR (METHANOL-d4) δ 8.69-8.61 (m, 2H), 8.38 (br ,1H), 8.16 (t, J = 8.0 Hz, 1H), 7.92 (d, J = 8.4 Hz, 1H), 7.05 (dd, J = 6.4 Hz, 2.4, 1H), 4.04 (d, J = 8.4 Hz, 2H), 3.78 (d, J = 8.4 hz, 2H), 2.64 (s, 1H), 1.94 (s, 1H). LC-MS: m/z 433.9 (M+H)+.
N-(2-Fluoro-pyridin-4-yl)-N'-(3-oxa-bicyclo[3AM]hex-6-yl)-6-(6-trifluoromethyU^
[l,3,5]triazine-2,4-diamine
Figure imgf000195_0003
1H NMR (METHANOL-d ) δ 8.68-8.66 (m, 1H), 8.24-7.97 (m, 4H), 7.50 (d, J = 5.2 Hz, 1H), 4.12 (d, J = 8.4 Hz, 2H), 3.83 (d, J = 8.0 Hz, 2H), 2.71 (s, 1H), 2.05-1.99 (m, 2H). LC-MS: m/z 433.9 (M+H)+. Compound 507 - N-(3-Oxa-bicyclo[3.1.0]hex-6-yl)-N'-(5-trifluoromethyl-pyridin-3-yl)-6-(6- trifluoromethyl-pyridin-2-yl)-[l,3,5]triazine-2,4-diamine
Figure imgf000196_0001
1H NMR (METHANOL-d4) δ 9.38 (br, 1H), 8.82-8.42 (m, 4H), 8.24 (d, J = 8.4 Hz, 1H), 4.05 (d, J = 8.4 Hz, 2H), 3.79 (d, J = 8.4 Hz, 2H), 2.81 (s, 1H), 2.15 (s, 2H). LC-MS: m/z 484.3 (M+H)+. Compound 508 - N-(2-Fluoro-pyridin-4-yl)-N'-(3-oxa-bicyclo[3.1.0]hex-6-yl)-6-(6- trifluoromethyl-pyridin-2-yl)-[l,3,5]triazine-2,4-diamine
Using the standard procedure described above except replacing t-BuONa by CS2CO3 to yield the title compound.
Figure imgf000196_0002
1H NMR (METHANOL-d ) δ 8.48-8.50 (d, J = 7.2 Hz, 1 H), 7.97-8.15 (m, 3 H), 7.79-7.96 (m, 1 H), 7.48-7.54 (m, 1 H), 4.13-4.15 (d, J = 8.8 Hz, 2 H), 3.83-3.85 (d, J = 8 Hz, 2 H), 2.78 (s, 1 H), 2.07-2.10 (d, J = 13.2 Hz, 2H). LC-MS: m/z 400.1 (M+H)+.
Compound 509 - N-(3-Oxa-bicyclo[3.1.0]hex-6-yl)-N'-(2-trifluoromethyl-pyridin-4-yl)-6-(6- trifluoromethyl-pyridin-2-yl)-[l,3,5]triazine-2,4-diamine
Using the standard procedure described above except replacing t-BuONa by CS2CO3 to yield the title compound.
Figure imgf000196_0003
1H NMR (METHANOL-d ) δ 8.47-8.66 (m, 2 H), 8.07-8.28 (m, 3 H), 7.76-7.78 (d, J = 8 Hz, 1 H), 4.06-4.14 (m, 2 H), 3.80-3.82 (d, J = 8.4 Hz, 2 H), 2.82 (s, 1 H), 2.04-2.16 (m, 2 H). LC-MS: m/z 450.1 (M+H)+. Compound 510 - N-(3-Oxa-bicyclo[3.1.0]hex-6-yl)-N'-(5-trifluoromethyl-pyridin-3-yl)-6-(6- trifluoromethyl-pyridin-2-yl)-[l,3,5]triazine-2,4-diamine
Using the standard procedure described above except replacing t-BuONa by CS2CO3 to yield the title compound.
Figure imgf000197_0001
1H NMR (METHANOL-d4) δ 9.05-9.20 (m, 1 H), 8.36-8.45 (m, 3 H), 7.96-7.97 (m, 1 H), 7.57- 7.60 (d, J = 7.6 Hz, 1 H), 4.04-4.06 (d, J = 8.4 Hz, 2 H), 3.75-3.77 (d, J = 8.4 Hz, 2 H), 2.78 (s, 1 H), 1.94 (s, 2 H). LC-MS: m/z 450.1 (M+H)+.
Compound 511 - 6-(6-Chloro-pyridin-2-yl)-N-(5-fluoro-pyridin-3-yl)-N'-(3-oxa- bicyclo[3.1.0]hex-6-yl)-[l,3,5]triazine-2,4-diamine
Figure imgf000197_0002
1H NMR (DMSO-d6) δ 10.50-10.60 (m, IH), 8.79-8.91 (m, IH), 8.43-8.48 (m, 2H), 8.19-8.29 (m., 2H), 8.05-8.11 (m, IH), 7.67-7.73 (m, IH), 3.95-4.06 (m, 2H), 3.68-3.70 (m, 2H), 3.32-3.33 (m, IH), 1.95 (s, 2 H). LC-MS: m/z 400.2 (M+H)+.
Compound 512 - 6-(6-Chloro-pyridin-2-yl)-N-(6-fluoro-pyridin-3-yl)-N'-(3-oxa- bicyclo[3.1.0]hex-6-yl)-[l,3,5]triazine-2,4-diamine
Figure imgf000197_0003
1H NMR (DMSO-d6) δ 10.36 (br, IH), 8.76-8.93 (m, IH), 8.30-8.43 (m, 3H), 8.04-8.10 (m., IH), 7.70-7.72 (m, IH), 7.13-7.20 (m, IH), 3.96-3.94 (m, 2H), 3.65-3.70 (m, 2H), 3.32-3.33 (m, IH), 2.09 (s, 2 H). LC-MS : m/z 400.2 (M+H)+.
Compound 513 - 6-(6-Chloro-pyridin-2-yl)-N-[2-(l,l-difluoro-ethyl)-pyridin-4-yl]-N'-isopropyl- [l,3,5]triazine-2,4-diamine
Figure imgf000198_0001
1H NMR (METHANOL-d4) δ 8.51-8.14 (m, 3H), Ί .96-1.59 (m, 3H), 4.52-4.26 (m, IH), 1.97 (t, J = 18.8 Hz, 2H), 1.31 ( , J = 6.4 Hz, 6H). LC-MS: m/z 406.3 (M+H) +.
Compound 514 - 2-{4-[4-(6-Chloro-pyridin-2-yl)-6-isopropylamino-[l,3,5]triazin-2-ylamino]- pyridin-2-yl}-propan-2-ol
Figure imgf000198_0002
1H NMR (METHANOL-d4) δ 8.48-8.30 (m, 3H), 7.99-7.95(m, IH), 7.77-7.61 (m, 2H), 4.51-4.37 (m, IH), 1.57 (s., 6H), 1.30 (d., J = 6.4 Hz, 6H). LC-MS: m/z 400.3 (M+H) +.
Compound 515 - N-(3,5-Difluoro-phenyl)-N'-(2-methyl-cyclopropyl)-6-pyridin-2-yl- [l,3,5]triazine-2,4-diamine
Figure imgf000198_0003
1H NMR (METHANOL-d ) δ 8.72-8.48 (m, 2H), 8.08-7.57 (m, 4H), 6.58 (s, IH), 2.27-2.57 (m, IH), 1.20 (s., 3H), 0.99-0.75 (m, 2H), 0.64-0.51 (s, H). LC-MS: m/z 455.2 (M+H) +.
Compound 516 - N-(2-Methyl-cyclopropyl)-6-pyridin-2-yl-N'-(2-trifluoromethyl-pyridin-4-yl)- [l,3,5]triazine-2,4-diamine
Figure imgf000198_0004
1H NMR (METHANOL-d ) δ 8.73-7.98 (m, 6H), 7.61-7.58 (m, IH), 2.79-2.54 (m, IH), 1.20 (d, J = 6.0 Hz, 3H), 0.85-0.81 (m., IH), 0.71-0.67 (m, 2H). LC-MS: m/z 388.3 (M+H) +. Compound 517 - N-(2,2-Dimethyl-propyl)-6-pyridin-2-yl-N'-(2-trifluoromethyl-pyridin-4-yl)- [l,3,5]triazine-2,4-diamine
Figure imgf000199_0001
1H NMR (METHANOL-d4) δ 8.75-8.49 (m, 4H), 8.03-7.76 (m, IH), Ί .62-1.59 (m, 2H), 3.41 (s, 2H), 0.99 (s., 9H). LC-MS: m/z 404.3 (M+H) +.
Compound 518 - 3-[4-(6-Chloro-pyridin-2-yl)-6-isopropylamino-[l,3,5]triazin-2-ylamino]-N- -trifluoro-ethyl)-benzenesulfonamide
Figure imgf000199_0002
1H NMR (DMSO-d6) δ 8.74 (s, IH), 8.70-8.40 (m, IH), 8.37-8.30 (m, IH), 8.30-8.11 (m, IH), 8.09-8.01 (m., IH), 7.84-7.82 (m, IH), 7.69 (m, IH), 7.54 (m, IH), 7.48-7.44 (m, IH), 4.33-4.22 (m, 1 H), 3.72-3.62 (m, 2H), 1.23-1.20 (d, J = 12 Hz, 6H). LC-MS : m/z 501.8 (M+H)+.
Compound 520 - l-[4-(3,5-Difluoro-phenylamino)-6-(6-trifluoromethyl-pyridin-2-yl)- [l,3,5]triazin-2-ylamino]-propan-2-ol
Figure imgf000199_0003
1H NMR (METHANOL-d4) δ 8.66-8.68 (m, IH), 8.19-8.23 (m, IH), 7.96-7.98 (m, IH), 7.51-7.57 (m., 2H), 6.57-6.60 (m, IH), 3.56-3.61 (d, J = 20 Hz, 2 H), 1.29 (s, 6 H). LC-MS : m/z 441.2 (M+H)+.
Compound 521 - N-(2,2-Dimethyl-propyl)-N'-pyrimidin-5-yl-6-( 6-trifluoromethyl-pyridin-2-yl)- [l,3,5]triazine-2,4-diamine
Figure imgf000200_0001
1H NMR (METHANOL-d4) δ 9.28-9.31 (m, 2H), 8.79-8.82 (m, IH), 8.67-8.69 (m, IH), 8.19-8.23 (m, IH), 7.96-7.98 (m, IH), 3.37-3.45 (m, IH), 3.30-3.37 (m, IH), 1.01 (s, 9 H). LC-MS : m/z 405.3 (M+H)+.
Compound 522 - N2-isopropyl-N4-(2-(trifluoromethyl)pyridin-4-yl)-6-(4- (trifluoromethyl)pyrimidin-2-yl)-l,3,5-triazine-2,4-diamine
Using the standard procedure described above except replace t-BuONa by CS2CO3 to give the title compound.
Figure imgf000200_0002
1H NMR (DMSO-d6): δ 10.63-10.81-10.95 (m, IH), 9.36-9.39 (m, IH), 8.73 (s, IH), 8.08-8.56 (m, 3H), 7.84-7.85 (m, IH), 4.14-4.19 (m, IH), 1.20-1.24 (m, 6H). LC-MS: m/z 444.8 (M+H)+.
Compound 523 - N2-neopentyl-N4-(2-(trifluoromethyl)pyridin-4-yl)-6-(4- (trifluoromethyl)pyrimidin-2-yl)-l,3,5-triazine-2,4-diamine
Using the standard procedure described above except replace t-BuONa by CS2CO3 to yield the title compound.
Figure imgf000200_0003
1H NMR (DMSO-d6): δ 10.70-10.95 (m, IH), 9.23 (d, J = 6.0 Hz, IH), 8.86 (s, IH), 8.36-8.76 (m, 3H), 7.64-7.66 (m, IH), 3.29-3.35 (m, 2H), 0.90-1.0.95 (m, 9H). LC-MS: m/z 473.2 (M+H)+. Compound 524 - N-(2-Methoxy-propyl)-6-(6-trifluoromethyl-pyridin-2-yl)-N'-(2- trifluoromethyl-pyridin-4-yl)-[l,3,5]triazine-2,4-diamine
Figure imgf000201_0001
IH NMR (METHANOL-d4) δ 8.75-8.77 (m, IH), 8.66-8.67 (m, IH), 8.50-8.52 (m, IH), 8.36-8.38 (m, IH), 8.1.7-8.18 (m, IH), 7.91-7.92 (m., IH), 3.52-3.80 (m, 3H), 3.45 (s., 3H), 1.27-1.255 (d., J = 6.0 Hz, 2H). LC-MS: m/z 474.2 (M+H)+.
Compound 526 - N-(2-Methoxy-l-methyl-ethyl)-6-(6-trifluoromethyl-pyridin-2-yl)-N'-(2- trifluoromethyl-pyridin-4-yl)-[l,3,5]triazine-2,4-diamine
Figure imgf000201_0002
1H NMR (METHANOL-d ) δ 8.69-8.67 (m, IH), 8.61-8.29 (m, 2H), 8.22-7.87 (m, 3H), 4.62-4.37 (m, IH), 3.57-3.46 (m., 2H), 3.31 (s, 3H), 1.33-1.30 (m, 3H). LC-MS: m/z 473.9 (M+H)+.
Compound 527 - 2-[4-(6-Trifluoromethyl-pyridin-2-yl)-6-(2 rifluoromethyl-pyridin-4-ylamino)- [l,3,5]triazin-2-ylamino]-propan-l-ol
Figure imgf000201_0003
1H NMR (METHANOL-d4) δ 8.73-8.48 (m, 3H), 8.23-7.92 (m, 3H), 4.62-4.29 (m, IH), 3.70-3.67 (m, 2H), 1.335-1.319 (d, J = 6.4 Hz, 3H). LC-MS: m/z 459.9 (M+H)+.
Compound 528 - N-(3-Methoxy-propyl)-N'-(2-trifluoromethyl-pyridin-4-yl)-6-(6- tri uoromethyl-pyridin-2-yl)-[l,3,5]triazine-2,4-diamine
Figure imgf000201_0004
1H NMR (METHANOL-d4) δ 8.67-8.69 (m, 1 H), 8.50-8.61 (m, 2 H), 8.19-8.23 (m,l H), 7.93- 7.99(m, 2 H), 3.61-3.69 (m, 2 H), 3.54-3.56 (m, 2 H), 3.30-3.37(m, 1 H), 1.93-1.99 (m, 2 H). LC- MS: m/z 474.3 (M+H)+.
Compounds 529 - N-(Tetrahydro-furan-3-yl)-N'-(2-trifluoromethyl-pyridin-4-yl)-6-(6- trifluoromethyl-pyridin-2-yl)-[l,3,5]triazine-2,4-diamine
Figure imgf000202_0001
1H NMR (METHANOL-d4) δ 8.66-8.68 (m, IH), 8.62-8.66 (m, IH), 8.49-8.51 (m,lH), 8.18- 8.22(m, 2H), 7.95-7.97 (m, IH), 4.60-4.66 (m, IH), 3.99-4.05(m, 2H), 3.79-3.82 (m, 2H), 2.04- 2.39(m, 2H). LC-MS: m/z 472.3 (M+H)+.
Compounds 530 - 2,2-Dimethyl-3-[4-(6-trifluoromethyl-pyridin-2-yl)-6-(2-trifluoromethyl- pyridin-4-ylamino)-[l,3,5]triazin-2-ylamino]-propan-l-ol
Figure imgf000202_0002
1H NMR (METHANOL-d4) δ 8.74-8.70 (m, IH), 8.67-8.52 (m, 2H), 8.29-7.90 (m, 3H), 3.51-3.41 (m, 2H), 3.34-3.33 (m., IH), 3.23 (s, IH), 1.03-0.92 (m, 6 H). LC-MS: m/z 488.3 (M+H)+.
Compound 531 - N-(2-Methyl-tetrahydro-furan-2-ylmethyl)-6-(6-trifluoromethyl-pyridin-2-yl)- '-(2-trifluoromethyl-pyridin-4-yl)-[l,3,5]triazine-2,4-diamine
Figure imgf000202_0003
1H NMR (METHANOL-d4) δ 8.71-8.24 (m, 3H), 8.23-7.84 (m, 3H), 3.97-3.90 (m, 2H), 3.78-3.58 (m, 2H), 2.03-1.97 (m., 2H), 1.78-1.74 (m, IH), 1.31 (s, 3H). LC-MS: m/z 500.3 (M+H) +. Compound 532 - N-(2-Methyl-cyclopropyl)-6-(6-trifluoromethyl-pyridin-2-yl)-N'-(2- trifluoromethyl-pyridin-4-yl)-[l,3,5]triazine-2,4-diamine
Figure imgf000203_0001
1H NMR (METHANOL-d4) δ 8.70-8.19 (m, 3H), 8.06-7.98 (m, 3H), 2.67-2.64 (m, IH), 1.25-1.21 (m, 3H), 1.21-0.98 (m., IH), 0.88-0.80 (m, IH), 0.62-0.51 (m, IH). LC-MS: m/z 456.2 (M+H) +. Compound 533 - N-(l-Methyl-cyclopropyl)-6-(6-trifluoromethyl-pyridin-2-yl)-N'-(2- trifluoromethyl-pyridin-4-yl)-[l,3,5]triazine-2,4-diamine
Figure imgf000203_0002
1H NMR (METHANOL-d4) δ 8.85-8.65 (m, 2H), 8.48 (s, IH), 8.20-8.16 (m, IH), 7.96-7.82 (m, 2H), 1.55 (s, 3H), 0.93-0.90 (m, 2H), 0.85-0.82 (m, 2 H). LC-MS: m/z 456.2 (M+H)+.
Compound 534 - 4-[4-Isopropylamino-6-(4-trifluoromethyl-pyrimidin-2-yl)-[l,3,5]triazin-2- ylamino]-pyridine-2-carbonitrile
Using the standard procedure described above except replacing t-BuONa by CS2CO3 to yield the title compound.
Figure imgf000203_0003
1H NMR (METHANOL-d ) δ 9.33-9.31 (m, IH), 8.65 (d, J = 6.4 Hz, IH), 8.47 (dd, J = 7.2 Hz, 5.6 Hz, IH), 8.07 (d, J = 4.8 Hz, IH), 7.96-7.95 (m, IH), 4.30-4.27 (m, IH), 1.32 (dd, J = 12 Hz, 6.0 Hz, 6H). LC-MS: m/z 402.2 (M+H)+.
Compound 535 - N-( 6-Fluoro-pyridin-3-yl)-N'-isopropyl-6-(4-trifluoromethyl-pyrimidin-2-yl)- [l,3,5]triazine-2,4-diamine
Figure imgf000204_0001
1H NMR (METHANOL-d4) δ 9.30 (d, J = 4.8 Hz, 1H), 8.62-8.53 (m, 2H), 8.05 (d, J = 5.2 Hz, 1H), 7.08-7.07 (m, 1H), 4.25-4.22 (m, 1H), 1.28 (dd, J = 10.8 Hz, 6.4 Hz, 6H). LC-MS: m/z 395.2 (M+H)+.
Compound 536 - N-Isopropyl-N'-(5-trifluoromethyl-pyridin-3-yl)-6-(4-trifluoromethyl- pyrimidin-2-yl)-[l,3,5]triazine-2,4-diamine
Using the standard procedure described above except replacing t-BuONa by CS2CO3 to yield the title compound.
Figure imgf000204_0002
1H NMR (METHANOL-d ) δ 9.31-9.33 (d, J = 4.8 Hz, 1 H), 8.98-9.11 (m, 1 H), 8.52 (s, 1 H), 8.06-8.07 (d, J = 4 Hz, 1 H), 4.26-4.63 (m, 2 H), 1.28-1.34 (m, 6 H). LC-MS: m/z 445.3 (M+H)+. Compound 537 - N-(2-Fluoro-pyridin-4-yl)-N'-isopropyl-6-(4-trifluoromethyl-pyrimidin-2-yl)- [l,3,5]triazine-2,4-diamine
Using the standard procedure described above except replacing t-BuONa by CS2CO3 to yield the title compound.
Figure imgf000204_0003
1H NMR (METHANOL-d ) δ 9.41-9.42 (m, 1 H), 8.14-8.20 (m, 2 H), 7.59-7.82 (m, 1 H), 4.35- 4.38 (m, 2 H), 1.32-1.41 (m, 6 H). LC-MS: m/z 395.2 (M+H)+.
Compound 539 - l-(4-(5,6-difluoropyridin-3-ylamino)-6-( 6-(trifluoromethyl)pyridin-2-yl)-l,3,5- triazin-2-ylamino)-2-methylpropan-2-ol
Figure imgf000205_0001
1H NMR (METHANOL-d4) δ 8.61-8.75 (m, IH), 8.01-8.43 (m, 4H), 3.48 (s, 2H), 1.21 (s, 6H). LC-MS : m/z 442.2 (M+H)+.
Compound 540 - 1-[4-( 6-Fluoro-5-methyl-pyridin-3-ylamino )-6-( 6-trifluoromethyl-pyridin-2-yl)- [l,3,5]triazin-2-ylamino]-2-methyl-propan-2-ol
Figure imgf000205_0002
1H NMR (METHANOL-d4) δ 8.94 (s, IH), 8.78 (d, J = 7.6 Hz, IH), 8.35 (t, J = 8.0 Hz, IH), 8.14 (d, J = 7.6 Hz, IH), 7.65-7.86 (m, 3H), 4.41-4.48 (m, IH), 3.20 (d, J = 7.2 Hz, 2H), 1.37 (d, J = 6.4 Hz, 6H), 0.98-1.06 (m, IH), 0.53-0.57 (m, 2H), 0.17-0.21 (m, 2H). LC-MS: m/z 493.1 (M+H)+. Compound 541 - l-{[4-(3,5-Difluoro-phenylamino)-6-(6-trifluoromethyl-pyridin-2-yl)- [l,3,5]triazin-2-ylamino]-methyl}-cyclopropanol
Figure imgf000205_0003
1H NMR (DMSO-d6) δ 8.628-8.543 (m, IH), 8.336-8.281 (m, IH), 8.107-8.088 (d,J =7.6 Hz, 2H), 7.788-7.767 (d, J = 8.4 Hz, IH), 1.30 (d, J = 6.2 Hz, IH), 6.842-6.797 (m, 1Η),5.503-5.428 (d, J = 30 Hz, IH), 3.629-3.567 (m, 2H), 0.666-0.584 (m, 2H). LC-MS: m/z 439.0 (M+H)+.
Compound 542 - 2-{3-[4-Isopropylamino-6-(6-trifluoromethyl-pyridin-2-yl)-[l,3,5]triazin-2- ylamino j-phenylj-propan-2-ol
Figure imgf000205_0004
1H NMR (METHANOL-d4) δ 8.82-8.79 (m, IH), 8.77-8.75 (m, IH), 8.48-8.42 (m, IH), 8.23-8.20 (m, IH), 7.63-7.57 (m, 3H), 4.43-4.26 (m, IH), 1.656-1.573 (d, J = 33.2 Hz, 3H), 1.288-1.188 (d, J=40 Hz 3H). LC-MS: m/z 433.1 (M+H)+.
Compound 543 - N-(l-Methyl-lH-pyrazol-4-yl)-6-(6-trifluoromethyl-pyridin-2-yl)-N'-(2- trifluoromethyl-pyridin-4-yl)-[l,3,5]triazine-2,4-diamine
Figure imgf000206_0001
1H NMR (METHANOL-d4) δ 8.71-8.69 (m, IH), 8.58-8.31 (m, 4H), 8.19-7.99 (m, 2H), 7.70-7.65 (m, IH), 3.92 (s, 3H). LC-MS: m/z 481.37 (M+H)+.
Compound 544 - N-(2-Methyl-2H-pyrazol-3-yl)-6-(6-trifluoromethyl-pyridin-2-yl)-N'-(2- trifluoromethyl-pyridin-4-yl)-[l,3,5]triazine-2,4-diamine
Figure imgf000206_0002
1H NMR (METHANOL-d4) δ 8.75-8.32 (m, 4H), 8.25-8.00 (m, 2H), 7.53 (s, IH), 6.44 (s, IH), 3.83 (s, 3 H). LC-MS: m/z 482.3 (M+H)+.
Compound 546 - N2-(thiazol-5-yl)-6-(6-(trifluoromethyl)pyridin-2-yl)-N4-(2- (trifluoromethyl)pyridin-4-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000206_0003
1H NMR (METHANOL-d4) δ 8.7-8.9 (m, IH), 8.65 (m, IH), 8.35-8.55 (m, IH), 8.05-8.3 (m, 2H), 8.0 (m, IH), 7.75 (m, IH). LC-MS: m/z 485.2 (M+H)+.
Compound 547 - N-(Tetrahydro-furan-3-ylmethyl)-N'-(2-trifluoromethyl-pyridin-4-yl)-6-(6- trifluoromethyl-pyridin-2-yl)-[l,3,5]triazine-2,4-diamine
Figure imgf000207_0001
1H NMR (METHANOL-d4) δ 8.78-8.76 (d, J = 8 Hz IH), 8.70-8.68 (d, J = 5.6 Hz IH), 8.53-8.52 (m, IH), 8.43-8.37 (m, IH), 8.22-8.20 (m, IH), 7.92-7.91 (m, IH), 3.95-3.93 (m, IH), 3.92-3.88 (m, IH), 3.86-3.85 (m, lH),3.78-3.77(m, 3H), 2.73-2.71 (ηι,.ΙΗ), 2.18-2.15 (m, IH), 1.77-1.75 (m, IH). LC-MS: m/z 486.2 (M+H) +.
Compound 548 - 3-[4-(6-Trifluoromethyl-pyridin-2-yl)-6-(2 rifluoromethyl-pyridin-4-ylamino)- [l,3,5]triazin-2-ylamino]-butan-2-ol
Figure imgf000207_0002
1H NMR (METHANOL-d4) δ 8.60-8.40 (m, 3H), 8.13-7.80 (m, 3H), 4.32-4.05 (m, IH), 3.88-3.79 (m, IH), 1.23-1.12 (m, 6H). LC-MS: m/z 474.3 (M+H)+
Compound 549 - N-(3-Methyl-oxetan-3-yl)-6-(6-trifluoromethyl-pyridin-2-yl)-N'-(2- trifluoromethyl-pyridin-4-yl)-[l,3,5]triazine-2,4-diamine
Figure imgf000207_0003
1H NMR (METHANOL-d4) δ 8.71-8.54 (m, IH), 8.49-8.52 (m, 2H), 8.25-8.21 (m, IH), 8.14-7.89
(m, 2H), 4.65-4.64 (m, 2H), 1.85 (s, 3 H). LC-MS : m/z 472.3 (M+H)+
Compound 550 - N-(3-Methyl-oxetan-3-ylmethyl)-6-(6-trifluoromethyl-pyridin-2-yl)-N'-(2- trifluoromethyl-pyridin-4-yl)-[l,3,5]triazine-2,4-diamine
Figure imgf000208_0001
1H NMR (METHANOL-d4) δ 8.72-8.52 (m, 3H), 8.26-7.99 (m, 3H), 4.74-4.67 (m, 2H), 4.45-4.42 (m, 2H), 3.87-3.82 (m, 2H), 1.43 (s, 3 H). LC-MS : m/z 486.3 (M+H)+
Compound 551 - N-(2-Difluoromethyl-pyridin-4-yl)-N'-isopropyl-6-( 6-trifluoromethyl-pyridin-2- -[l,3,5]triazine-2,4-diamine
Figure imgf000208_0002
1H NMR (METHANOL-d4) δ 8.71-8.68 (m, 1H), 8.53 (s, 1H), 8.44 (m, 1H), 8.23-7.78 (m, 3H), 6.84-6.56 (m., 1H), 4.31 (m, 1H), 1.36-1.34 (d, J = 8 Hz, 6H). LC-MS : m/z 426.2 (M+H)+
Compound 552 - 2-Methyl-3-[4-( 6-trifluoromethyl-pyridin-2-yl)-6-(2-trifluoromethyl-pyridin-4- ylamino )-[l,3,5]triazin-2-ylamino ]-propan-l-ol
Figure imgf000208_0003
1H NMR (METHANOL-d4) δ 8.72-8.69 (m, 1H), 8.56-8.49 (m, 2H), 8.28-7.96 (m, 3H), 4.64-3.29 (m, 4H), 2.07-2.03 (m, 1H), 1.04-0.998 (m, 3 H). LC-MS : m/z 474.2 (M+H)+
Compound 554 - 5-[4-(2,2-Dimethyl-propylamino)-6-(4-trifluoromethyl-pyrimidin-2-yl)- [l,3,5]triazin-2-ylamino]-nicotinonitrile
Using the standard procedure described above except replacing t-BuONa by CS2CO3 yielded the title compound.
Figure imgf000209_0001
1H NMR (MeOH-d4) δ 9.42-9.46 (m, IH), 8.73-9.25 (m, 3H), 8.21-8.26 (m, IH), 3.49-3.51 (m, 2H), 1.00-1.07 (m, 9H). LC-MS: m/z 430.3 (M+H)+.
Compound 555 - N-Isopropyl-N'-(l-propyl-lH-pyrazol-4-yl)-6-(6-trifluoromethyl-pyridin-2-yl)- [l,3,5]triazine-2,4-diamine
Figure imgf000209_0002
1H NMR (METHANOL-d4) δ 8.67-8.65 (m, IH), 8.30-7.98 (m, 3H), 7.70-7.60 (m, IH), 4.50-4.20 (m, IH), 4.13-4.10 (m., 2H), 1.92-1.89 (m, 2H), 1.35-1.29 (m, 6H), 0.96-0.93 (t, 3H). LC-MS : m/z 407.3 (M+H)+
Compound 556 - N-(7-Oxa-bicyclo[2.2.1]hept-2-yl)-6-(6-trifluoromethyl-pyridin-2-yl)-N'-(2- trifluoromethyl-pyridin-4-yl)-[l,3,5]triazine-2,4-diamine
Figure imgf000209_0003
1H NMR (METHANOL-d4) δ 8.71-8.48 (m, 3H), 8.24-7.93 (m, 3H), 4.87-4.86 (m, IH), 4.70- 4.605 (m, IH), 4.43-4.18 (m, IH), 2.35-1.99 (m, 2 H), 1.78-1.23 (m, 4 H). LC-MS : m/z 498.2 (M+H)+
Compound 557 - N2-((tetrahydrofuran-3-yl)methyl)-N4-(2-(trifluoromethyl)pyridin-4-yl)-6-(4- (trifluoromethyl)pyrimidin-2-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000209_0004
1H NMR (MeOH-d4) δ 9.36-9.42 (m, IH), 8.50-8.69 (m, 2H), 8.20-8.21 (m, IH), 7.93-8.13 (m, IH), 3.64-3.98 (m, 6H), 2.71-2.77 (m, IH), 2.12-2.27 (m, IH), 1.73-1.81 (m, IH). LC-MS: m/z 487.3 (M+H)+.
Compound 558 - N2-(l-methoxypropan-2-yl)-N4-(2-(trifluoromethyl)pyridin-4-yl)-6-(4- (trifluoromethyl)pyrimidin-2-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000210_0001
1H NMR (MeOH-d4) δ 9.31 (d, J= 4.8 Hz, IH), 8.30-8.66 (m, 2H), 7.87-8.21 (m, 2H), 4.36-4.67 (m, IH), 3.49 (s, 3H), 1.28-1.34 (m, 3H). LC-MS: m/z 475.3 (M+H)+.
Compound 559 - N-Isopropyl-N'-[2-(l-methoxy-cyclopropyl)-pyridin-4-yl]-6-(6-trifluoromethyl- pyridin-2-yl)-[l,3,5]triazine-2,4-diamine
Figure imgf000210_0002
1H NMR (METHANOL-d ) δ 8.69-8.71 (d, J = 8 Hz, 1 H), 8.18-8.31 (m, 3 H), 7.93-7.98 (m, 1.3 H), 7.58-7.59 (d, J = 3.6 Hz, 0.7 H), 4.34-4.62 (m, 1 H), 3.39 (s, 3 H), 1.33-1.34 (d, J = 6 Hz, 1 H), 1.23-1.28 (m, 4 H). LC-MS : m/z 446.2 (M+H)+
Compound 560 - l-[4-[6-(l,l-Difluoro-ethyl)-pyridin-2-yl]-6-(3,5-difluoro-phenylamino)- [l,3,5]triazin-2-ylamino]-2-methyl-propan-2-ol
Figure imgf000210_0003
1H NMR (METHANOL-d ) δ 8.65-8.88 (d, J = 7.6 Hz, 1 H) 8.30-8.35 (d, J = 20 Hz, 1 H), 8.10-
8.12 (d, J = 8 Hz, 1 H), 7.50-7.58 (m, 2 H), 6.86-6.90 (m, 1 H), 3.58-3.64 (d, J = 24 Hz, 1 H), 2.13-
2.25 (m, 3 H), 1.35-1.37 (d, J = 6.8 Hz, 6 H). LC-MS : m/z 437.1 (M+H)+
Compound 561 - N-(3-Chloro-5-methanesulfonyl-phenyl)-N'-isopropyl-6-(6-trifluoromethyl- pyridin-2-yl)-[l,3,5]triazine-2,4-diamine
Figure imgf000211_0001
IH NMR (METHANOL-d4) δ 8.70-8.67 (m, 2H), 8.24-8.17 (m, IH), 8.04 (m, IH), 7.97-7.95 (m, IH), 7.58-7.55 (s., IH), 4.34-4.28 (m, IH), 3.19 (s, 3H), 1.33-1.31 (d, J=6.4 Hz, 6H). LC-MS : m/z 487.2 (M+H)+
Compound 562 - 2-Methyl-2-[4-( 6-trifluoromethyl-pyridin-2-yl)-6-(2-trifluoromethyl-pyridin-4- ylamino )-[l,3,5]triazin-2-ylamino ]-propan-l-ol
Figure imgf000211_0002
1H NMR (METHANOL-d4) δ 8.70-8.68 (d, J = 8 Hz IH), 8.64-7.88 (m, 5H), 8.53-8.52 (m, IH), 3.83(s, 3H), 1.523-1.496 (d, J = 10.8 Hz 6H). LC-MS : m/z 474.3 (M+H) +.
Compound 563 - N-(2-Cyclopropyl-pyridin-4-yl)-N'-isopropyl-6-( 6-trifluoromethyl-pyridin-2-yl)- [l,3,5]triazine-2,4-diamine
Figure imgf000211_0003
1H NMR (METHANOL-d4) δ 8.78-8.76 (m, IH), 8.48-8.35 (m, 2H), 8.17-8.06 (m, 3H), 4.39-4.36
(m, IH), 1.49-1.38 (m, 8H), 1.21-1.19 (m, 2H). LC-MS : m/z 416.1 (M+H)+ .
Compound 564 - N-tert-Butyl-N'-( 2-cyclopropyl-pyridin-4-yl)-6-( 6-trifluoromethyl-pyridin-2-yl)-
[l,3,5]triazine-2,4-diamine
Figure imgf000211_0004
1H NMR (METHANOL-d ) δ 8.68-8.66 (m, IH), 8.21-8.19 (m, 2H), 7.98-7.64(m, 3H), 2.15-2.11
(m, IH), 1.59 (s, 9H), 1.11-1.01 (m, 4H). LC-MS : m/z 430.1 (M+H)+. Compound 565 - N-(2-Cyclopropyl-pyridin-4-yl)-N'-(l-methyl-cyclopropyl)-6-(6-trifluoromethyl- pyridin-2-yl)-[l,3,5]triazine-2,4-diamine
Figure imgf000212_0001
1H NMR (METHANOL-d4) δ 8.69-8.67 (m, IH), 8.25-8.19 (m, 2H), 8.01-7.86 (m, 3H), 2.15-2.11 (m, IH), 1.57-1.56 (m, IH), 1.17-1.12 (m, 2H), 1.08-1.02 (m, 2H), 0.94-0.90 (m, 2H), 0.87-0.85 (m, 2H). LC-MS : m/z 428.1 (M+H)+.
Compound 566 - {l-[4-(6-Trifluoromethyl-pyridin-2-yl)-6-(2-trifluoromethyl-pyridin-4- ylamino )-[l,3,5]triazin-2-ylamino ]-cyclopropyl}-methanol
Figure imgf000212_0002
1H NMR (METHANOL-d4) δ 8.74-8.69 (m, 2H), 8.52-8.48 (m, IH), 8.25-7.58 (m, 3H), 3.79 (s, 2H), 1.02-0.95 (m, 4H). LC-MS : m/z 494.2 (M+H)+.
Compound 567 - N-tert-Butyl-N'-[2-(l,l-difluoro-ethyl)-pyridin-4-yl]-6-(6-trifluoromethyl- pyridin-2-yl)-[l,3,5]triazine-2,4-diamine
Figure imgf000212_0003
1H NMR (METHANOL-d4) δ 8.72-8.44 (m, 3H), 8.25-7.77 (m, 3H), 2.05-1.95 (m, 3H), 1.58 (s, 9 H). LC-MS : m/z 454.1 (M+H)+.
Compound 568 - 2-[4-(6-Trifluoromethyl-pyridin-2-yl)-6-(2 rifluoromethyl-pyridin-4-ylamino)- [l,3,5]triazin-2-ylamino]-cyclopropanol
Figure imgf000213_0001
1H NMR (METHANOL-d4) δ 8.31-8.90 (m, 3H), 8.15-8.30 (m, 2H), 7.93-8.05 (m, IH), 3.43-3.55 (m, IH), 2.90-3.10 (m, IH), 1.10-1.25 (m, IH), 0.89-0.99 (m, IH). LC-MS : m/z 458.2 (M+H)+. Compound 569 - 2-[4-(6-Trifluoromethyl-pyridin-2-yl)-6-(2 rifluoromethyl-pyridin-4-ylamino)- [l,3,5]triazin-2-ylamino]-cyclopropanol
Figure imgf000213_0002
1H NMR (METHANOL-d4) δ 8.35-8.90 (m, 3H), 8.13-8.34 (m, 2H), 7.97-8.05 (m, IH), 3.47-3.55 (m, IH), 2.72-3.01 (m, IH), 1.08-1.25 (m, IH), 0.90-0.99 (m, IH). LC-MS : m/z 458.2 (M+H)+. Compound 570 - N2-(3-fluoro-5-(methylsulfonyl)phenyl)-N4-isopropyl-6-(6- (trifluoromethyl)pyridin-2-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000213_0003
1H NMR (METHANOL-d ) δ 8.70-8.62 (m, 2 H), 8.21-7.84 (m, 3 H), 7.35-7.33 (m, 1 H), 4.34- 4.31 (m, 1 H), 3.16 (s, 3 H), 1.31 (dd, 6 H). LC-MS: m/z 470.0 (M+H)+.
Compound 571 - N2-isobutyl-N4-(3-(methylsulfonyl)phenyl)-6-(6-(trifluoromethyl)pyridin-2-yl)- -triazine-2,4-diamine
Figure imgf000213_0004
1H NMR (METHANOL-d4) : δ 8.7-8.9 (m, 2 H), 8.3-8.5 (m, 1 H), 8.0-8.2 (m, 1 H), 7.6-7.86 (m, 3
H), 3.5 (m, 2 H), 3.15 (S, 3 H), 1.0-1.1 (d, J = 16 Hz, 6 H). LC-MS : m/z 467.1 (M+H)+. Compound 572 - N2-(2-chloropyridin-4-yl)-N4 sopropyl-6-(6-(tnfluoromethyl)pyridin-2-yl)- l,3,5-triazine-2,4-diamine
Figure imgf000214_0001
1H NMR (DMSO-d4) δ 10.2-10.5 (m, l.OH), 8.85-8.65 (m, 1 H), 8.6 (m, 1 H), 8.25-8.45 (m, 3 H), 8.1 (m, 1 H), 7.2 (m, 1 H), 4.1-4.4 (m, 1 H), 1.2 (d, J = 6.4 Hz, 6 H). LC-MS : m/z 410.1 (M+H)+. Compound 573 - l-[4-[2-(l,l-Difluoro-ethyl)-pyridin-4-ylamino]-6-(6^rifluoromethyl-pyridin-2- yl)-[l,3,5]triazin-2-ylamino]-2-methyl-propan-2-ol
Figure imgf000214_0002
1H NMR (METHANOL-d ) δ 8.72-8.42 (m, 3H), 8.24-7.74 (m, 3H), 3.64-3.60 (m, 2H), 2.05-1.94
(m, 3H), 2.34-1.91 (m, 4H), 1.30-1.29 (m, 6 H). LC-MS : m/z 492.1 (M+Na)+.
Compound 574 - l-{4-[4-Isopropylamino-6-(6-trifluoromethyl-pyridin-2-yl)-[l,3,5]triazin-2- ylamino]-pyridin-2-yl}-propan-l-one
Figure imgf000214_0003
1H NMR (METHANOL-d ) δ 8.69 (s, 0.7 H), 8.63-8.64 (d, J = 8 Hz, 1 H), 8.38-8.40 (dd, = 5.2 Hz, = 9.2 Hz, 1 H), 8.13-8.18 (q, J = 8 Hz, 1 H)„ 7.78-8.03 (m, 2 H), 4.22-4.36 (m, 1 H), 3.12- 3.16 (m, 2 H), 1.25-1.29 (m, 6 H), 1.11-1.14 (m, 3 H). LC-MS : m/z 375.1 (M+H)+.
Compound 576 - 6-[6-(l,l-Difluoro-ethyl)-pyridin-2-yl]-N-[2-(l,l-difluoro-ethyl)-pyridin-4-yl]- N '-isopropyl-[ 1, 3, 5 Jtriazin e-2, 4-diam in e
Figure imgf000215_0001
1H NMR (METHANOL-d4) δ 8.78-8.80 (d, J = 6 Hz, 1 H), 8.69-8.71 (d, J = 8.4 Hz, 2 H), 8.26- 8.53 (m, 1 H), 8.05-8.19 (m, 2 H), 4.39-4.60 (m, 1 H), 2.10-2.24 (m, 6 H), 1.40-1.46 (m, 6 H). LC-MS : m/z 436.3 (M+H)+.
Compound 577 - 4-[4-(6-Trifluoromethyl-pyridin-2-yl)-6-(2 rifluoromethyl-pyridin-4-ylamino)- [l,3,5]triazin-2-ylamino]-piperidine-l-carboxylic acid methyl ester
Figure imgf000215_0002
1H NMR (METHANOL-d4) δ 8.30-8.78 (m, 3H), 7.82-8.29 (m, 3H), 4.10-4.39 (m, 3H), 3.73 (s, 3H), 2.99-3.18 (m, 2H), 2.02-2.16 (m, 2H), 1.53-1.65 (m, 2H). LC-MS : m/z 543.3 (M+H)+. Compound 578 - l-{4-[4-(6-Trifluoromethyl-pyridin-2-yl)-6-(2-trifluoromethyl-pyridin-4- ylamino)-[l,3,5]triazin-2-ylamino]-piperidin-l-yl}-ethanone
Figure imgf000215_0003
1H NMR (METHANOL-d4) δ 8.62-8.87 (m, 2H), 8.30-8.60 (m, 2H), 7.88-8.29 (m, 2H), 4.31-4.60 (m, 2H), 3.95-4.10 (m, IH), 3.37-3.43 (m, IH), 2.90-3.19 (m, IH), 2.10-2.30 (m, 5H), 1.58-1.83 (m, 2H). LC-MS : m/z 527.2 (M+H)+.
Compound 580 - N-(l-Methanesulfonyl-piperidin-4-yl)-6-( 6-trifluoromethyl-pyridin-2-yl)-N'-(2- trifluoromethyl-pyridin-4-yl)-[l,3,5]triazine-2,4-diamine
Figure imgf000215_0004
1H NMR (METHANOL-d4) δ 8.67-8.93 (m, 2H), 8.38-8.59 (m, 2H), 7.92-8.31 (m, 2H), 4.19-4.52 (m, 1H), 3.70-3.88 (m, 2H), 3.08 (t, J = 10.4 Hz, 6H), 2.93 (s, 3H), 2.18-2.32 (m, 2H), 1.77-1.98 (m, 2H). LC-MS : m/z 563.3 (M+H)+.
Compound 581 - N-Isopropyl-N'-[2-(l-methyl-cyclopropyl)-pyridin-4-yl]-6-(6-trifluoromethyl- pyridin-2-yl)-[l,3,5]triazine-2,4-diamine
Figure imgf000216_0001
1H NMR (DMSO-d6) δ 8.73-8.69 (d, J= 17.6 Hz 1H), 8.26-8.16 (m, 3H), 8.06-7.97 (m, 1H), 7.63- 7.62 (m, 1H), 4.38-4.34 (m, 1H), 1.54-1.52 (s, 3H), 1.35-1.26 (m, 6H), 1.18-1.16 (m, 2H), 0.90- 0.97 (m, 2H). LC-MS : m/z 430.1 (M+H)+.
Compound 582 - 6-[6-(l,l-Difluoro-ethyl)-pyridin-2-yl]-N-isopropyl-N'-(2-trifluoromethyl- pyridin-4-yl)-[l,3,5]triazine-2,4-diamine
Figure imgf000216_0002
1H NMR (METHANOL-d4) δ 8.63-8.50 (m, 3H), 8.26-8.09 (m, 1H), 7.97-7.87 (m, 2H), 4.50-4.29 (m, 1H), 2.14 (t, J = 13.2 Hz, 3H), 1.35 (d, J = 8.8 Hz, 6H). LC-MS : m/z 440.1(M+H)+.
Compound 583 - 6-(6-(l,l-difluoroethyl)pyridin-2-yl)-N2-(3,5-difluorophenyl)-N4-isopropyl- -triazine-2,4-diamine
Figure imgf000216_0003
1H NMR (METHANOL-d ) δ 8.53 (t, 1 H), 8.09 (t, 1 H), 7.86-7.84 (m, 1 H), 7.58-7.56 (m, 1 H), 6.60-6.56 (m, 1 H), 4.28-4.25 (m, 1 H), 2.17-2.04 (m, 3 H), 1.33-1.29 (m, 6 H). LC-MS: m/z 407.2 (M+H)+. Compound 584 - N2-(cyclopropylmethyl)-6-(6-(l,l-difluoroethyl)pyridin-2-yl)-N4-(3,5- difluorophenyl)-l,3,5-triazine-2,4-diamine
Figure imgf000217_0001
1H NMR (METHANOL-d4) δ 8.51 (t, 1 H), 8.01 (t, 1 H), 7.84 (t, 1 H), 7.56-7.54 (m, 1 H), 6.56 (t, 1 H), 3.42-3.36 (1 H), 2.10 (t, 3 H), 1.18-1.16 (m, 1 H), 0.57-0.51 (m, 2 H), 0.33-0.29 (m, 2 H). LC-MS: m/z 419.2 (M+H)+.
Compound 585 - N2-(tert-butyl)-6-(6-(l,l-difluoroethyl)pyridin-2-yl)-N4-(3,5-difluorophenyl)- -triazine-2,4-diamine
Figure imgf000217_0002
1H NMR (METHANOL-d4) δ 8.85-8.49 (m, 1 H), 8.09-8.06 (m, 1 H), 7.83 (d, 1 H), 7.52-7.48 (m, 2 H), 6.61-6.56 (m, 1 H), 2.10 (t, 3 H), 1.53 (s, 9 H). LC-MS: m/z 421.1 (M+H)+.
Compound 586 - l-(4-((4-((cyclopropylmethyl)amino)-6-(6-(l,l-difluoroethyl)pyridin-2-yl)- -triazin-2-yl)amino)pyridin-2-yl)cyclopropanecarbonitrile
Figure imgf000217_0003
1H NMR (METHANOL-d4) δ 8.62 (d, 1 H), 8.16-7.56 (m, 4 H), 4.47-4.23 (m, 1 H), 3.62-3.61 (m, 1 H), 1.34-1.04 (m, 10 H). LC-MS: m/z 405.2 (M+H)+.
Compound 587 - N2-(tetrahydro-2H-pyran-4-yl)-6-(6-(trifluoromethyl)pyridin-2-yl)-N4-(2- (trifluoromethyl)pyridin-4-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000218_0001
1H NMR (METHANOL-d4) δ 8.7-8.25 (m, 3 H), 8.25-7.7 (m, 3 H), 4.4-4.1 (m, 1 H), 4.0 (r 3.65-3.5 (m, 2 H), 2.1-2.0 (m, 2 H), 1.8-1.6 (m, 2 H). LC-MS : m/z 486.3 (M+H)+.
Compound 588 - 2-((4-(6-(trifluoromethyl)pyridin-2-yl)-6-((2-(trifluoromethyl)pyridin-4- yl)amino )-l,3,5-triazin-2-yl)amino )cyclopentanol
Figure imgf000218_0002
1H NMR (METHANOL-d4) δ 8.85-8.6 (m, 2.0 H), 8.5-8.0 (m, 4 H), 4.4-4.15 (m, 2 H), 2.4-1.6 (m, 6 H). LC-MS : m/z 486.0 (M+H)+.
Preparation of 3-[4-(6-Chloro-pyridin-2-yl)-6-isopropylamino-[l,3,5]triazin-2-ylamino]-N- cyclopropyl-benzamide
Step 1: Preparation of methyl 3-(4-(6-chloropyridin-2-yl)-6-(isopropylamino)-l,3,5-triazin-2-yl- amino) benzoate
To a solution of 4-chloro-6-(6-chloropyridin-2-yl)-N-isopropyl-l,3,5-triazin-2-amine (134 mg, 0.47 mmol) in toluene (4 mL) was added methyl 3-aminobenzoate (85.6 mg, 0.57 mmol), CS2CO3 (306.9 mg, 0.94 mmol), BINAP (29.33 mg, 0.047 mmol) and Pd2(dba)3 (43.13 mg, 0.047 mmol). The mixture was purged with nitrogen three times and stirred at 110°C for 40 min under M.W. irradiation. TLC (PE: EA = 1: 1) showed the reaction was complete. The mixture was partitioned between H20 (150 mL) and EA (50 mL). The organic layer was separated, dried over Na2S04, filtered and concentrated in vacuo. The residue was purified by combi flash to give methyl 3-(4-(6- chloropyridin-2-yl)-6-(isopropylamino)-l,3,5-triazin-2-yl amino)benzoate as a yellow solid.
Figure imgf000218_0003
Step 2: Preparation of 3-(4-(6-chloropyridin-2-yl)-6-(isopropylamino)-l,3,5-triazin-2- ylamino)benzoic acid
To a solution of methyl 3-(4-(6-chloropyridin-2-yl)-6-(isopropylamino)-l,3,5-triazin-2-y-l amino)benzoate (112 mg, 0.28 mmol) in MeOH (2 mL) was added NaOH (0.28 mL, 3 N). The mixture was stirred at room temperature for 3 h. TLC (PE: EA = 1: 1) showed the reaction was complete. The mixture was concentrated in vacuo. The residue was acidified with 1 N HC1 to pH = 6 and extracted with CH2CI2 (50 mL * 3). The combined extracts were concentrated to give 3- (4- (6-chloropyridin-2-yl)-6-(isopropylamino)-l,3,5-triazin-2-ylamino) benzoic acid
as a yellow solid.
Figure imgf000219_0001
Step3: 3-[4-(6-Chloro^yridin-2-yl)-6 sopropylamino-[l,3,5]triazin-2-ylamino]-N- cyclopropyl- benzamide
To a solution of 3-(4-(6-chloropyridin-2-yl)-6-(isopropylamino)-l,3,5-triazin-2-ylamino) benzoic acid (104 mg, 0.27 mmol) in DMF (4 mL) was added HATU (205 mg, 0.54 mmol), NMM (81.93 mg, 0.81 mmol). The mixture was purged with nitrogen and stirred at room temperature overnight. LCMS showed the reaction was complete. The mixture was poured into brine (150 mL) and extracted with EA (50 mL * 2). The combined extracts were dried over Na2S04, filtered and concentrated in vacuo. The residue was purified by a standard method to give the title compound.
Figure imgf000219_0002
1H NMR (METHANOL-d4) δ 8.57-8.40 (m, 2H), 8.01 (t, J = 7.9 Hz, 1H), 7.82 (d, J = 8.0 Hz, 1H),
7.64 (d, J = 8.0 Hz, 1H), 7.48-7.40 (m, 2H), 4.33-4.30 (m, 1H), 2.89-2.87 (m, 1H), 1.32 (d, J = 6.4
Hz, 6H), 0.87-0.82 (m, 2H), 0.68-0.64 (m, 2H). LC-MS : m/z 424.2 (M+H)+.
Example 8. Preparation of Compounds of Formula I Wherein Ring A is Substituted Aryl or
Heteroaryl.
The compounds of this Example are prepared by the general method in Scheme 8, set forth below.
Figure imgf000220_0001
Preparation of 2-Methyl-l-[4-(2-trifluoromethyl-pyridin-4-ylamino )-6-( 4-trifluoromethyl- pyrimidin-2-yl)-[l,3,5]triazin-2-ylamino]-propan-2-ol
Example 8, step 1: Preparation of 4-chloro-6-(4-trifluoromethyl- pyrimidin-2-yl)-[l,3,5]triazin- 2-yl]-(2-trifluoromethyl-pyridin-4-yl)-amine. To a solution of 2,4-dichloro-6-(4- (trifluoromethyl)pyrimidin-2-yl)-l,3,5-triazine (1) (981 mg, 3.31 mmol) in THF (80 mL) was added 2-(trifluoromethyl)pyridin-4-amine (4) (590 mg, 3.64 mmol) and NaHC03 (556 mg, 6.6 mmol). The mixture was stirred at refluxing for 18 hours. The mixture was concentrated and poured to water, extracted with ethyl acetate, dried over sodium sulphate, filtered and concentrated to give a residue, which was purified by Si02 chromatography to give 4-chloro-6-(4- trifluoromethyl- pyrimidin-2-yl)-[l,3,5]triazin-2-yl]-(2-trifluoromethyl-pyridin-4-yl)-amine (0.45 32%) as a yellow solid.
Figure imgf000220_0002
LCMS: m/z 422.2 (M+H)+
The following intermediate was similarly prepared according to Example 8, step 1:
4-chloro-6-(6-(trifluoromethyl)pyridin-2-yl)-N-(2-(trifluoromethyl)pyri^
amine
Figure imgf000220_0003
LCMS: m/z 421.2 (M+H)+
4-chloro-6-( 6-( l,l-difluoroethyl)pyridin-2-yl)-N-(2-( trifluoromethyl)pyridin-4-yl)-l,3,5-triazin-2- amine
Figure imgf000221_0001
LCMS: m/z 416.3 (M+H)+
Example 8, step 2: 2-Methyl-l-[4-(2-trifluoromethyl-pyridin-4-ylamino)-6-(4-trifluoromethyl- pyrimidin-2-yl)-[l,3,5]triazin-2-ylamino]-propan-2-ol
To a solution of [4-chloro-6-(4-trifluoromethyl-pyrimidin-2-yl)-[l,3,5]triazin-2-yl]-(2- trifluoromethyl-pyridin-4-yl)-amine (90 mg, 0.21 mmol) in anhydrous THF (2 mL) was added 1- amino-2-methyl-propan-2-ol (28.5 mg, 0.32 mmol). The mixture was stirred at ambient temperature for 4 hour. After concentration, the residue was purified by a standard method to give 2-methyl-l-[4-(2-trifluoromethyl-pyridin-4-ylamino)-6-(4-trifluoromethyl-pyrimidin-2-yl)- [ 1 ,3,5]triazin-2-ylamino] -propan-2-ol.
Compound 589 - 2-methyl-l-((4-((2-(trifluoromethyl)pyridin-4-yl)amino)-6-(4- (Mfluoromethyl)pyrimidin-2-yl)-l,3,5-triazin-2-yl)amino)propan-2-ol
Figure imgf000221_0002
1H NMR (MeOH-d4) δ 9.41-9.48 (m, 1H), 8.49-8.72 (m, 2H), 7.92-8.27 (m, 2H), 3.65-3.69 (m, 2H), 1.37 (s, 6H). LC-MS: m/z 475.3 (M+H)+.
The following compounds were prepared in a similar manner to the synthetic sequence in Scheme 8, Steps 1 and 2, using appropriate reagents and synthetic intermediates:
Compound 590 - 2-((4-((2-(trifluoromethyl)pyridin-4-yl)amino)-6-(4- (trifluoromethyl)pyrimidin-2-yl)-l,3,5-triazin-2-yl)amino)propan-l-ol
Figure imgf000222_0001
1H NMR (MeOH-d4) δ 9.35-9.41 (m, IH), 8.39-8.64 (m, 2H), 8.18-8.21 (m, IH), 7.93-8.13 (m, IH), 4.34-4.46 (m, IH), 3.67-3.80 (m, 2H), 1.31-1.39 (m, 3H). LC-MS: m/z 461.3 (M+H)+. Compound 591 - 2-Methyl-3-[4-( 6-trifluoromethyl-pyridin-2-yl)-6-(2-trifluoromethyl-pyridin-4- ylamino )-[l,3,5]triazin-2-ylamino ]-butan-2-ol
Figure imgf000222_0002
1H NMR (METHANOL-d4) δ 8.71-8.66 (m, 2H), 8.25-8.61 (m, IH), 8.24-7.84 (m, 3H), 4.24-4.22 (m, IH), 1.31-1.28 (s, 3 H). LC-MS: m/z 488.0 (M+H)+.
Compound 592 - N-tert-Butyl-N'-(3-fluoro-5-methanesulfonyl-phenyl)-6-(6-trifluoromethyl- pyridin-2-yl)-[l,3,5]triazine-2,4-diamine
Figure imgf000222_0003
1H NMR (METHANOL-d4) δ 8.75-8.73 (m, IH), 8.24-8.21 (m, 2H), Ί .99-1.92 (m, 2H),
(m, IH), 3.20 (s, 3H), 1.57(s, 9H). LC-MS: m/z 485.1 (M+H)+.
Compound 593 - N-Cyclopropylmethyl-N'-(3-fluoro-5-methanesulfonyl-phenyl)-6-(6- trifluoromethyl-pyridin-2-yl)-[l,3,5]triazine-2,4-diamine
Figure imgf000222_0004
1H NMR (METHANOL-d4) δ 8.71-8.60 (m, 2H), 8.22-7.95 (m, 3H), 7.34-7.33 (m, IH), 3.44-3.39 (m, 2H), 3.20 (s, 3H), 1.23 (m, IH), 0.36-0.10 (m, 2H). LC-MS: m/z 483.1 (M+H)+. Compound 594 - l-((4-(6-(l,l-difluoroethyl)pyridin-2-yl)-6-((2-(trifluoromethyl)pyrMin-4- yl)amino )-l,3,5-triazin-2-yl)amino )-2-methylpropan-2-ol
Figure imgf000223_0001
1H NMR (METHANOL-d4) δ 8.61-8.21 (m, 3 H), 8.15-7.85 (m, 3 H), 3.59 (d, 2 H), 2.11 (t, 3 H), 1.27 (d, 6 H). LC-MS: m/z 470.2 (M+H)+.
Compound 595 - N2-(cyclopropylmethyl)-6-(6-(l,l-difluoroethyl)pyridin-2-yl)-N4-(2- (trifluoromethyl)pyridin-4-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000223_0002
1H NMR (METHANOL-d4) δ 8.66-8.28 (m, 3 H), 8.22-7.85 (m, 3 H), 3.42 (dd, 2 H), 2.11 (t, 3 H), 1.21 (br, 1 H), 0.59-0.55 (m, 2 H), 0.36-0.31 (m, 2 H). LC-MS: m/z 452.2 (M+H)+.
Compound 596 - N2-(tert-butyl)-6-(6-(l,l-difluoroethyl)pyridin-2-yl)-N4-(2-(l,l- difluoroethyl)pyridin-4-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000223_0003
1H NMR (METHANOL-d4) δ 8.55-8.41 (m, 3 H), 8.11-8.07 (m, 1 H), 7.86-7.76 (m, 2
1.93 (m, 6 H), 1.56 (s, 9 H). LC-MS: m/z 450.2 (M+H)+.
Compound 597 - N2-(cyclopropylmethyl)-6-(6-(trifluoromethyl)pyridin-2-yl)-N4-(2- (trifluoromethyl)pyridin-4-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000223_0004
1H NMR (METHANOL-d4) δ 8.75-8.73 (d, 2 H), 8.55-8.38 (m, 1 H), 8.28-8.22 (m, 1 H), 8.02 (d, 1 H), 7.88 (br, 1 H), 3.53-3.41 (dd, 2 H), 1.21 (br, 1 H), 0.64-0.58 (m, 2 H), 0.46-0.33 (m, 2 H). LC-MS: m/z 456.2 (M+H)+.
Compound 598 - N2-(cyclopropylmethyl)-N4-(3,5-difluorophenyl)-6-(6-(trifluoromethyl)pyridin- -yl)-l,3,5-triazine-2,4-diamine
Figure imgf000224_0001
1H NMR (METHANOL-d ) δ 8.68-865 (m, IH), 8.22-8.18 (m, IH), 7.97-7.95 (m, IH), Ί .56-1.52 (m, 2H), 6.61-6.56 (m, IH), 3.44-3.38 (m, 2H), 1.20-1.18 (m, IH), 0.57-0.55 (m, 2H), 0.34-0.33 (m, 2H). LC-MS: m/z 423.2 (M+H)+.
Compound 599 - N2-(3-chloro-5-(methylsulfonyl)phenyl)-N4-(cyclopropylmethyl)-6-(6- (trifluoromethyl)pyridin-2-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000224_0002
1H NMR (METHANOL-d ) δ 8.73-8.71 (m, 2H), 8.24-8.20 (t, J = 8 Hz, IH), 8.10 (s, IH), 7.99- 7.97 (d, J = 8 Hz, IH), 7.61 (s, IH), 3.49-3.43 (m, 2H), 3.19 (s, IH), 1.23-1.19 (m, IH), 0.58-0.55 (m, 2H), 0.39-0.35 (m, 2H). LC-MS: m/z 499.2 (M+H)+.
Compound 600 - N2-(tert-butyl)-N4-(3-chloro-5-(methylsulfonyl)phenyl)-6-(6- (trifluoromethyl)pyridin-2-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000224_0003
1H NMR (METHANOL-d ) δ 8.68-8.66 (m, 2H), 8.43-8.28 (m, IH), 8.18-8.14 (m, 2H), 7.94-7.92 (d, J = 7.6 Hz, IH), 7.58-7.53 (m, IH), 3.16 (s, 3H), 1.53 (s, 9H). LC-MS: m/z 501.2 (M+H)+. Compound 601 - N2-(tert-butyl)-N4-(3,5-difluorophenyl)-6-(6-(trifluoromethyl)pyridin-2-yl)- l,3,5-triazine-2,4-diamine
Figure imgf000225_0001
1H NMR (METHANOL-d4) δ 8.64-8.62 (m, IH), 8.20-8.16 (m, IH), 7.95-7.93 (m, IH), 7.50-7.48 (m, 2H), 6.60-6.53 (m, IH), 1.53 (s, 9H). LC-MS: m/z 425.5 (M+H)+.
Compound 602 - N2-(tert-butyl)-6-(6-(trifluoromethyl)pyridin-2-yl)-N4-(2- (trifluoromethyl)pyridin-4-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000225_0002
1H NMR (METHANOL-d4) δ 8.67-8.64 (m, IH), 8.49-8.48 (m, IH), 8.21-8.17 (m., 2H), 7.96-7.94 (m, IH), 7.81 (br.s., IH), 1.55 (s, 9H). LC-MS: m/z 458.2 (M+H)+.
Compound 603 - N2-(3,5-difluorophenyl)-N4 sopropyl-6-(6-(trifluoromethyl)pyridin-2-yl)- -triazine-2,4-diamine
Figure imgf000225_0003
1H NMR (METHANOL-d ) δ 8.35-8.16 (d, IH), 7.79-7.65 (m, IH), 7.58-7.56 (s, 2H), 7.30- 7.20(d,lH),6.10-6.0(s, 1Η),4.50-4.27 (m, IH), 1.33-1.31 (d, 6H). LC-MS: m/z 411.1 (M+H)+. Compound 604 - N2-(cyclopropylmethyl)-N4-(2-(l,l-difluoroethyl)pyridin-4-yl)-6-(6- (trifluoromethyl)pyridin-2-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000225_0004
1H NMR (METHANOL-d4) δ 8.68 (d,l H), 8.50-8.18 (m, 3 H), 8.02-7.73 (m,2 H), 3.42 (dd, 2 H), 2.01 (t, 2 H), 1.24-1.16 (m, 1 H), 0.58-0.55 (m, 2 H), 0.35-0.33 (m, 2H). LC-MS: m/z 452.1 (M+H)+.
Compound 605 - l-((4-(6-(l,l-difluoroethyl)pyridin-2-yl)-6-((2-(l,l-difluoroethyl)pyridin-4- yl)amino )-l,3,5-triazin-2-yl)amino )-2-methylpropan-2-ol
Figure imgf000226_0001
1H NMR (METHANOL-d ) δ 8.58-8.13 (m 3 H), 8.11-7.76 (m, 3 H), 3.60 (d, 2 H), 2.17-1.93 (m, 6 H), 1.28 (d, 6 H). LC-MS: m/z 466.1 (M+H)+.
Compound 606 - l-(4-((4-(tert-butylamino)-6-(6-(l,l-difluoroethyl)pyridin-2-yl)-l,3,5 riaz yl)amino)pyridin-2-yl)cyclopropanecarbonitrile
Figure imgf000226_0002
1H NMR (METHANOL-d4) δ 8.71-8..5 (m, IH), 8.4-8.2 (m, IH), 8.1 (m, IH), 7.9 (m, H), 7.6 (m, IH), 2.15-2.06 (t, J = 18 Hz, 3H), 1.78-1.74 (d, J = 16 Hz, 4H), 1.55 (s, 9H). LC-MS: m/z 450.2 (M+H)+.
Compound 607 - N2-(cyclopropylmethyl)-N4-(3-(methylsulfonyl)phenyl)-6-(6- (trifluoromethyl)pyridin-2-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000226_0003
1H NMR (DMSO, T=273+80K) δ 10.03 (s, IH), 8.78 (s, IH), 8.59-8.57 (m, IH), 8.28-8.24 (m, IH), 8.04-7.97 (m, 2H), 7.59-7.84 (m, 3H), 3.35 (br.s., 2H), 3.17 (S, 3H), 1.15-1.14 (m, IH), 0.48- 0.46 (m, 2H), 0.32-0.31 (m, 2H). LC-MS: m/z 465.2 (M+H)+. Compound 608 - l-(4-((4-(tert-butylamino)-6-(6-(trifluoromethyl)pyridin-2-yl)-l,3,5 ria^ yl)amino)pyridin-2-yl)cyclopropanecarbonitrile
Figure imgf000227_0001
1H NMR (METHANOL-d4) δ 8.87-8.85 (m, IH), 8.7-8.11 (m, 2H), 7.96-7.87 (m, IH), 7..585-
7.583(m,lH) 1.8-1.70 (d, 4H),1.59-1.54(m,6H). LC-MS: m/z 455.1 (M+H)+.
Compound 609 - N2-(3-chloro-5-(methylsulfonyl)phenyl)-N4-(cyclopropylmethyl)-6-(6-(l,l- difluoroethyl)pyridin-2-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000227_0002
1H NMR (METHANOL-d4) δ 8.65 (s, IH), 8.54-8.51 (m, IH), 8.06-8.04 (t, J = 7.8 Hz, 2H), 7.84- 7.82 (d, J = 1.6 Hz, IH), 7.57-7.56 (m, IH), 3.39-3.37 (m, 2H), 3.14 (s, 3H), 2.13-20.3 (t, J = 19.2 Hz, IH), 1.18-1.13 (m, IH), 0.54-0.50 (m, 2H), 0.32-0.31 (m, 2H). LC-MS: m/z 501.2 (M+H)+. Compound 610 - N2-(cyclopropylmethyl)-6-(6-(l,l-difluoroethyl)pyridin-2-yl)-N4-(2-(l,l- difluoroethyl)pyridin-4-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000227_0003
1H NMR (METHANOL-d ) δ 8.56-8.13 (m, 3H), 8.11-7.77 (m, 3H), 3.45-3.40 (m, 2 H), 2.15-1.94 (m, 6 H), 1.22-1.18 (m, 1 H), 0.58-1.19 (m, 1 H), 0.59-0.54 (m, 2 H), 0.36-0.31 (m, 2 H). LC-MS: m/z 448.2 (M+H)+.
Compound 611 - N2-(cyclopropylmethyl)-6-(6-(l,l-difluoroethyl)pyridin-2-yl)-N4-(3- (methylsulfonyl)phenyl)-l,3,5-triazine-2,4-diamine
Figure imgf000228_0001
1H NMR (METHANOL-d4) δ 8.96 (s, 1 H), 8.58-8.55 (m, 1 H), 8.10-7.78 (m, 3 H), 7.62-7.55 (m, 2 H), 3.44-3.41 (m, 2 H), 3.14 (d, 3 H), 2.11 (t, 3 H), 1.20-1.17 (m, 1 H), 0.57-0.52 (m, 2 H), 0.36- 0.33 (m, 2 H). LC-MS: m/z 461.2 (M+H)+.
Compound 612 - N2-(cyclopropylmethyl)-6-(6-(l,l-difluoroethyl)pyridin-2-yl)-N4-(3-fluoro-5- (methylsulfonyl)phenyl)-l,3,5-triazine-2,4-diamine
Figure imgf000228_0002
1H NMR (METHANOL-d ) δ 8.58-8.13 (m, 2 H), 8.12-7.86 (m, 2 H), 7.36-7.32 (m, 1 H), 3.46- 3.41 (m, 2 H), 3.19 (d, 3 H), 2.13 (t, 3 H), 1.24-1.18 (m, 1 H), 0.59-0.56 (m, 2 H), 0.37-0.35 (m, 2 H). LC-MS: m/z 479.2 (M+H)+.
Compound 613 - 6-(6-(l,l-difluoroethyl)pyridin-2-yl)-N2-(3-fluoro-5-(methylsulfonyl)phenyl)- -isopropyl-l,3,5-triazine-2,4-diamine
Figure imgf000228_0003
1H NMR (METHANOL-d4) δ 8.57 (d, 2 H), 8.13-7.86 (m, 3 H), 7.37-7.32 (m, 1 H), 4.37-4.34 (m, 1 H), 3.19 (d, 3 H), 2.18-2.06 (m, 3 H), 1.35-1.32 (m, 6 H). LC-MS: m/z 467.2 (M+H)+.
Compound 614 - N2-(3-chloro-5-(methylsulfonyl)phenyl)-6-(6-(l,l-difluoroethyl)pyridin-2-yl)- -isopropyl-l,3,5-triazine-2,4-diamine
Figure imgf000228_0004
1H NMR (METHANOL-d4) δ 8.73-8.33 (m, 2 H), 8.11 (t, 2 H), 7.87 (d, 1 H), 7.61 (s, 1 H), 4.48- 4.28 (m, 1 H), 3.20 (d, 3 H), 2.13 (t, 3 H), 1.34 (t, 6 H). LC-MS: m/z 488.2 (M+H)+.
Compound 615 - N2-(tert-butyl)-N4-(3-chloro-5-(methylsulfonyl)phenyl)-6-(6-(l,l- difluoroethyl)pyridin-2-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000229_0001
1H NMR (METHANOL-d4) δ 8.57-8.56 (m, 1 H), 8.43-8.25 (m, 2 H), 8.12-8.06 (m, 1 H), 7.85 (d, 1 H), 7.61 (s, l H), 3.17 (s, 3 H), 2.11 (t, 3 H), 1.56 (s, 9 H). LC-MS: m/z 497.2 (M+H)+.
Compound 616 - N2-(tert-butyl)-6-(6-(l,l-difluoroethyl)pyridin-2-yl)-N4-(3-fluoro-5- (methylsulfonyl)phenyl)-l,3,5-triazine-2,4-diamine
Figure imgf000229_0002
1H NMR (METHANOL-d ) δ 8.59-8.42, 8.13-8.05 (m, 2 H), 7.87 (d, 1 H), 7.39-7.34 (m, 1 H),
3.19 (s, 3 H), 2.18-2.06 (m, 3 H), 1.57 (s, 9 H). LC-MS: m/z 481.2 (M+H)+.
Compound 617 - 1-(4-((4-(( cyclopropylmethyl)amino )-6-( 6-( trifluoromethyl)pyridin-2-yl)-l,3,5- triazin-2-yl)amino)pyridin-2-yl)cyclopropanecarbonitrile
1H NMR (METHANOL-d4) δ 8.87-8.85 (m, 1H), 8.7-8.11 (m, 2H), 7.96-7.87 (m, 1H), 7.585- 7.583(m,lH) ,3.35 (br.s., 2H), 1.15-1.14 (m, 1H), 0.48-0.46 (m, 2H), 0.32-0.31 (m, 2H). LC-MS: m/z 453.1 (M+H)+.
Compound 618 - ( 4-((4-( ( cyclopropylmethyl)amino )-6-( 6-( l,l-difluoroethyl)pyridin-2-yl)-l,3,5- triazin-2-yl)amino)pyridin-2-yl)-2-methylpropanenitrile
Figure imgf000230_0001
1H NMR (METHANOL-d4) δ 8.60-8.56 (m, IH), 8.44-8.37 (m, 2H), 8.11-8.03 (m, IH), 7.87-7.85 (m, IH), 7.62-7.60 (m, IH), 3.45-3.43 (d, 2H), 2.15-2.06 (t, 3H), 1.78 (s, 6H), 1.21-1.16 (m, IH), 0.57-0.54 (m, 2H), 0.36-0.33 (m, 2H). LC-MS: m/z 451.2 (M+H)+.
Compound 619 - l-(4-((4-((cyclopropylmethyl)amino)-6-(6-(l,l-difluoroethyl)pyridin-2-yl)- -triazin-2-yl)amino)pyridin-2-yl)cyclopropanecarbonitrile
Figure imgf000230_0002
1H NMR (METHANOL-d ) δ 8.64-8.57 (t, IH), 8.54-8.53 (d, IH), 8.26-8.25 (d, IH), 8.09-8.05 (m, IH), 7.86-7.83 (m, IH), 7.45-7.42 (m, IH), 3.46-3.44 (d, 2H), 2.16-2.06 (q, 3H), 1.80-1.71 (m, 4H), 1.19-1.12 (m, IH), 0.56-0.53 (m, 2H), 0.37-0.34 (m, 2H). LC-MS: m/z 449.3 (M+H)+.
N2 sopropyl-6-(6-(2,2,2-trifluoroethylamino)pyridin-2-yl)-N4-(2-(trifluorome
-triazine-2,4-diamine
Figure imgf000230_0003
1H NMR (DMSO-d4): δ 10.6-10.2 (m, 1 H), 8.7-8.4 (m, 2 H), 8.4-7.8 (m, 2 H), 7.8-7.5 (m, 2 H), 7.4-7.2 (m, 1 H), 6.8 (m, 1 H), 4.5-4.0 (m, 3 H), 1.2 (d, J = 4.8 Hz, 1 H). LC-MS: m/z 473.2
(M+H)+.
The following compounds were prepared according to the general procedure shown in Scheme 4:
The following intermediates prepared according to Example 4, step 1, using appropriate reagents: Preparation of ( 4, 6-Dichloro-[l,3,5]triazin-2-yl)-oxetan-3-yl-amine
Using the standard procedure described above yielded the title compound which was directly used in the next step.
Figure imgf000231_0001
Preparation of (4,6-Dichloro-[l,3,5]triazin-2-yl)-(3-oxa-bicyclo[3.1.0]hex-6-yl)-amine
Using the standard procedure described above except DIPEA (leq) was added to give (4,6- Dichloro-[l,3,5]triazin-2-yl)-(3-oxa-bicyclo[3.1.0]hex-6-yl-amine as a white solid.
Figure imgf000231_0002
LCMS: m/z 247.1 (M+H)+.
The following intermediates were prepared according to Example 4, step 2:
Preparation of 4-chloro-6-( 2-fluoro-3-methoxyphenyl)-N-( oxetan-3-yl)-l,3,5-triazin-2-amine
Using the standard procedure described above yielded the title compound.
Figure imgf000231_0003
LCMS: m/z 311.0 (M+H)+.
Step 2-9: Preparation of 4-chloro-6-(2-fluoro-5-methoxyphenyl)-N-(oxetan-3-yl)-l,3,5- triazin-2- amine
Using the standard procedure described above yielded the title compound.
Figure imgf000231_0004
LCMS: m/z 311.1 (M+H)+.
Preparation of N-((lR,5S,6r)-3-oxabicyclo[3.1.0]hexan-6-yl)-4-chloro-6-(2-fluoro phenyl)-l,3,5- triazin-2-amine
Using the standard procedure described above yielded the title compound
Figure imgf000232_0001
LCMS: m/z 306.9 (M+H)+.
Preparation of 4-chloro-6-( 2-fluorophenyl)-N-isobutyl-l,3,5-triazin-2-
Using the standard procedure described yielded the title compound
Figure imgf000232_0002
LCMS: m/z 281.1 (M+H)+.
Preparation of 4-Chloro-6-( 6-fluoro-5-methoxyphenyl)-N-isopropyl-l,3,5-tri-azin-2-amine.
Usin the standard procedure described above yielded the title compound as a white solid.
Figure imgf000232_0003
LCMS: m/z 297.1 (M+H)+.
Preparation of 4-(3-(l-((tert-butyldimethylsilyl)oxy)cyclopropyl)phenyl)-6-chloro-N-isopropyl- l,3,5-triazin-2-amine. Using the standard procedure described above yielded the title compound as a colorless oil.
Figure imgf000233_0001
The following compounds were synthesized using Example 4, step 3 (Procedure C), utilizing appropriate intermediates and reagents:
Compound 621 - l-(4-(2-fluorophenyl)-6-(5-fluoropyridin-3-ylamino)-l,3,5-triazin-2-ylamino)- -methylpropan-2-ol
Figure imgf000233_0002
1H NMR (METHANOL-d4) δ 8.68-9.01 (m, 1H), 8.44-8.51 (m, 2H), 8.20-8.23 (m, 1H), 8.76-8.77 (m, 1H), 7.38-7.47 (m, 2H),7.76-7.81 (m, 2H), 3.56-3.61 (m, 2H), 1.27-1.31 (m, 6H). LC-MS: m/z 373.3 (M+H)+.
Compound 622 - l-(4-(2-fluorophenyl)-6-( 6-fluoropyridin-3-ylamino)-l,3,5-triazin-2-ylamino)- -methylpropan-2-ol
Figure imgf000233_0003
1H NMR (METHANOL-d4) δ 8.08-8.15 (m, 1H), Ί .96-1.91 (m, 2H), 7.83-7.89 (m, 1H), 7.51-7.54 (m, 2H), 7.21-7.31 (m, 2H),3.53-3.55 (m, 2H), 3.56-3.61 (m, 2H), 1.25-1.27 (m, 6H). LC-MS: m/z 373.2 (M+H)+.
Compound 623 - l-(4-(2-fluorophenyl)-6-(2-fluoropyridin-4-ylamino)-l,3,5-triazin-2-ylamino)- 2-methylpropan-2-ol
Figure imgf000234_0001
1H NMR (METHANOL-d4) δ 8.27-8.55 (m, IH), 8.25-8.27 (m, 2H), 7.77-7.78 (m, IH), 7.39-7.47 (m, 2H), 7.16-7.19 (m, 1H),3.51-3.53 (m, 2H), 1.28 (m, 6H). LC-MS: m/z 373.2 (M+H)+.
Compound 624- 6-(2-Fluoro-3-methoxy-phenyl)-N-oxetan-3-yl-N'-(2-trifluoromethyl-pyridin-4- -[l,3,5]triazine-2,4-diamine
Figure imgf000234_0002
1H NMR (DMSO-d6) δ 10.53-10.43 (m, IH), 8.89-7.92 (m, 4H), 7.55-7.48 (m, IH), 7.39-7.34 (m, IH), 7.25 (t, J = 8.25 Hz, IH), 5.07-5.01 (m, IH), 4.83-4.77 (m, 2H), 4.61 (t, J = 6.18 Hz, 2H), 3.88 (s, 3H). LC-MS: m/z 437.2 (M+H)+.
Compound 625 - 6-(2-Fluoro-phenyl)-N-(5-fluoro-pyridin-3-yl)-N'-oxetan-3-yl-[l,3,5]triazine- -diamine
Figure imgf000234_0003
1H NMR (DMSO-d6) δ 10.17-10.12 (m, IH), 8.77-7.98 (m, 5H), 7.61-7.59 (m, IH), 7.37-7.34 (m., 2H), 5.09-5.06 (m, IH), 4.81-4.80 (m, 2H), 4.62-4.61 (m, 2H). LC-MS: m/z 357.1 (M+H)+.
Compound 626 - 6-(2-Fluoro-phenyl)-N-( 6-fluoro-pyridin-3-yl)-N'-oxetan-3-yl-[l,3,5]triazine- -diamine
Figure imgf000234_0004
1H NMR (DMSO-d6) δ 10.06-9.59 (m, 1H), 8.71-8.29 (m, 3H), 8.07-7.95 (m, 1H), 7.61-7.56 (m., 1H), 7.34-7.28(m, 2H), 7.16-7.15 (m, 1H), 5.06-4.95 (m, 1H), 4.77-4.76 (m, 2H), 4.59-4.56 (m, 2H). LC-MS: m/z 357.1 (M+H)+.
Compound 627 - 6-(2-Fluoro-phenyl)-N-oxetan-3-yl-N'-(2-trifluoromethyl-pyridin-4-yl)- [l,3,5]triazine-2,4-diamine
Figure imgf000235_0001
1H NMR (METHANOL-d4) δ 8.56-8.47 (m, 2H), 8.17-7.89 (m, 2H), 7.58-7.53 (m, 1H), 7.31-7.21 (m., 2H), 5.34-5.24 (m, 1H), 5.01-4.99 (m, 2H), 4.80-4.73 (m, 2H). LC-MS: m/z 407.2 (M+H)+. Compound 628 - 6-(2-Fluoro-phenyl)-N-(2-fluoro-pyridin-4-yl)-N'-oxetan-3-yl-[l,3,5]triazine- 2,4-diamine
Figure imgf000235_0002
1H NMR (DMSO-d6) δ 10.45-10.39 (m, 1H), 8.86-8.68 (m, 1H), 8.08-7.69 (m, 5H), 7.37-7.33 (m., 2H), 5.11-5.09 (m, 1H), 4.85-4.80 (m, 2H), 4.64-4.59 (m, 2H). LC-MS: m/z 357.1 (M+H)+.
Compound 629 - 6-(2-Fluoro-phenyl)-N-oxetan-3-yl-N'-(5-trifluoromethyl-pyridin-3-yl)- [l,3,5]triazine-2,4-diamine
Figure imgf000235_0003
1H NMR (DMSO-d6) δ 10.34-10.20 (m, 1H), 9.25-8.50 (m, 3H), 8.06-8.00 (m, 1H), 7.77-7.72 (m., 1H), 7.39-7.25 (m, 2H), 5.10-4.99 (m, 1H), 4.79-4.56 (m, 2H), 4.59-4.52 (m, 2H). LC-MS: m/z 407.3 (M+H)+.
Compound 630 - 6-(2-Fluoro-5-methoxy-phenyl)-N-isopropyl-N'-(2-trifluoromethyl-pyridin-4- yl)-[l,3,5]triazine-2,4-diamine
Figure imgf000236_0001
1H NMR (METHANOL-d4) δ 8.70-7.82 (m, 3H), 7.67-7.61 (m, IH), 7.16-7.06 (m, 2H), 4.30-4.25 (m., IH), 3.84 (s, 3H), 4.26-4.23 (m, IH), 1.317-1.279 (d, J = 15.2 MHz, 3H). LC-MS: m/z 422.9 (M+H)+.
Compound 631 - 6-(2-Fluoro-3-methoxy-phenyl)-N-isopropyl-N'-(2-trifluoromethyl-pyridin-4- -[l,3,5]triazine-2,4-diamine
Figure imgf000236_0002
1H NMR (METHANOL-d ) δ 8.65-7.83 (m, 3H), 7.59-7.56 (m, IH), 7.24-7.16 (m, 2H), 4.28-4.25 (m., IH), 3.92 (s, 3H), 1.315-1.272 (d, J = 17.2 MHz, 3H). LC-MS: m/z 423.0 (M+H)+.
Compound 632 - 2-(4-((4-(2-fluorophenyl)-6-(isopropylamino)-l,3,5-triazin-2-yl)amino)pyridin- -yl)propan-2-ol
Figure imgf000236_0003
1H NMR (DMSO-d6) δ 8.30-8.08 (m, 3 H), 7.70-7.51 (m, 2 H), 7.29 (t, 1 H), 7.24-7.19 (dd, 1 H), 4.36-4.34 (m, 1 H), 1.57 (s, 6 H), 1.32-1.28 (m, 6 H). LC-MS: m/z 383.3(M+H)+.
Compound 633 - 2-Fluoro-3-[4-isopropylamino-6-(2-trifluoromethyl-pyridin-4-ylamino)- [l,3,5]triazin-2-yl]-phenol
Figure imgf000236_0004
1H NMR (METHANOL-d4) δ 8.70-8.68 (d, J =6 Hz, 1H), 8.56-8.49 (m, 1H), 7.90-7.89 (m, 1H), 7.59-7.57 (m., 1H), 7.33-7.23 (m, 2H), 4.39-4.35 (m, 1H), 1.407-1.391 (d, J = 6.4 Hz, 3H). LC- MS: m/z 409.3 (M+H)+.
Compound 634 - 4-Fluoro-3-[4-isopropylamino-6-(2-trifluoromethyl-pyridin-4-ylamino)- [l,3,5]triazin-2-yl]-phenol
Figure imgf000237_0001
1H NMR (METHANOL-d4) δ 8.70-8.68 (d, J =5.6 MHz, 1H), 8.56-8.53 (m, 1H), 7.91-7.89 (m, 1H), 7.58-7.55 (m., 1H), 7.27-7.15 (m, 2H), 4.40-4.35 (m, 1H), 1.40-1.39 (d, J = 6.4 MHz, 3H). LC-MS: m/z 409.1 (M+H)+.
Compound 635 - 6-(2-Fluoro-5-methoxy-phenyl)-N-oxetan-3-yl-N'-(2-trifluoromethyl-pyridin-4- -[l,3,5]triazine-2,4-diamine
Figure imgf000237_0002
1H NMR (DMSO-d6) δ 10.73-10.63 (m, 1H), 9.11-8.11 (m, 4H), 7.82-7.69 (m, 1H), 7.47 (t, J = 9.62 Hz, 1H), 7.35 (brs., 1H), 5.34-5.20 (m, 1H), 5.04-5.00 (m, 2H), 4.83-4.80 (m, 2H), 3.80 (s, 3H). LC-MS: m/z 437.3(M+H)+'
Compound 636 - 6-(2-Fluoro-phenyl)-N-(2-fluoro-pyridin-4-yl)-N'-(3-oxa-bicyclo[3.1.0]hex-6- -[l,3,5]triazine-2,4-diamine
Figure imgf000237_0003
1H NMR (DMSO-d6) δ 10.50-10.21 (m, 1H), 8.35-7.85 (m, 4H), Ί .62-1.52 (m, 2H), 7.37-7.29 (m, 2H), 3.96-3.88 (m., 2H), 3.69-3.61 (m, 2H), 2.66-2.49 (m, 1H), 1.94-1.87 (m, 2H). LC-MS: m/z 383.1 (M+H)+. Compound 637 - 6-(2-Fluoro-phenyl)-N-(6-fluoro-pyridin-3-yl)-N'-(3-oxa-bicyclo[3.1.0]hex-6- -[l,3,5]triazine-2,4-diamine
Figure imgf000238_0001
1H NMR (METHANOL-d4) δ 8.71-8.57 (m, IH), 8.30 (brs. IH), 8.18 (brs. IH), 7.81 (brs. IH), 7.50-7.43 (m., 2H), 7.21 (brs. IH), 4.12-4.02 (m, 2H), 3.81-3.75 (m, 2H), 2.80-2.68 (m, IH), 2.14- 2.09 (m, 2H). LC-MS: m/z 383.2 (M+H)+.
Compound 638 - 6-(2-Fluoro-phenyl)-N-(5-fluoro-pyridin-3-yl)-N'-(3-oxa-bicyclo[3.1.0]hex-6- -[l,3,5]triazine-2,4-diamine
Figure imgf000238_0002
1H NMR (METHANOL-d4) δ 8.67 (brs., 2H), 8.20-8.07 (m, 2H), 7.56 (brs., IH), 7.32-7.21 (m, 2H), 4.14-4.05 (m., 2H), 3.83-3.78 (m, 2H), 2.71-2.68 (m, IH), 2.00-1.96 (m,2H). LC-MS: m/z 383.1 (M+H)+.
Compound 639 - {3-[4-Isopropylamino-6-(2-trifluoromethyl-pyridin-4-ylamino)-[l,3,5]triazin-2- -phenyl}-methanol
Figure imgf000238_0003
1H NMR (METHANOL-d4) δ 8.37-8.41 (m, 3H), 8.31-8.28 (m, 2H), 7.53-7.53 (d, J = 6 Hz, IH), 7.46-7.45 (m, IH), 4.685 (s, 2H), 4.52-4.18 (m, IH), 1.31-1.30 (d, J=6.4 Hz, 6H). LC-MS: m/z 405.1 (M+H)+.
Compound 640 - 3-[4-Isopropylamino-6-( 2-trifluoromethyl-pyridin-4-ylamino )-[l,3,5]triazin-2- ylj-phenol
Figure imgf000239_0001
1H NMR (METHANOL-d4) δ 8.679-8.245 (m, 2H), 7.95-7.83 (m, 2H), 7.32-7.282 (m, 1H), 7. 6.98 (d, J = 8 Hz, 1H), 4.31-4.28 (m,lH), 1.34-1.25 (m, 6H). LC-MS: m/z 391.2 (M+H)+.
Compound 641 - 3-(4-((2-hydroxy-2-methylpropyl)amino)-6-((2-(trifluoromethyl)pyridin-4- yl)amino)-l,3,5-triazin-2-yl)phenol
Figure imgf000239_0002
1H NMR (METHANOL-d ) δ 8.72-8.70 (m, 1 H), 8.68-8.38 (m, 1 H), 8.28-7.96 (m, 1 H), 7.79- 7.70 (m, 2 H), 7.51-7.44 (m, 1 H), 7.23-7.17 (m, 1 H), 3.65 (d, 2 H), 1.36 (d, 6 H). LC-MS: m/z 421.2 (M+H)+.
Compound 642 - 5-(4-((3,5-difluorophenyl)amino)-6-(isopropylamino)-l,3,5-triazin-2- yl)benzene-l,3-diol
Figure imgf000239_0003
1H NMR (METHANOL-d4) δ 7.51-7.48 (m, 2 H), 7.30 (d, 2 H), 6.52-6.41 (m, 2 H), 4.23-4.21 (m, 1 H), 1.35-1.27 (m, 6 H). LC-MS: m/z 374.1 (M+H)+.
Compound 644 - 6-(3-Chloro-5-trifluoromethyl-phenyl)-N-isopropyl-N'-(2-trifluoromethyl- pyridin-4-yl)-[l,3,5]triazine-2,4-diamine
Figure imgf000239_0004
1H NMR (METHANOL-d4) δ 8.79-8.50 (m, 3H), 8.49-7.86 (m, 2H), 7.77-7.76 (m, 1H), 4.26-4.23 (m, 1H), 1.32-1.30 (d, 6H). LC-MS: m/z 477.1 (M+H)+.
Compound 645 - 6-( 6-aminopyridin-3-yl)-N2-(3,5-difluorophenyl)-N4-isopropyl-l,3,5-triazine- 2,4-diamine
Figure imgf000240_0001
1H NMR (DMSO-d6) δ 9.80 (d, 1 H), 8.87 (d, 1H), 8.52-7.29 (m, 5 H), 6.78-6.50 (m, 3 H), 4.29- 4.11 (m, 1 H), 1.20 (d, 6 H). LC-MS: m/z 358.2 (M+H)+.
Compound 646 - 3-(4-(tert-butylamino)-6-((3-fluoro-5-(methylsulfonyl)phenyl)amino)-l,3,5- triazin-2-yl)phenol
Figure imgf000240_0002
1H NMR (METHANOL-d4) δ 8.37-7.74 (m, 4 H), 7.25 (br, 2 H), 6.92 (br, 1 H), 3.13 (s, 3 H), 1.51 (s, 6 H). LC-MS: m/z 432.0 (M+H)+.
Compound 647 - 6-(3-chloro-5-fluorophenyl)-N2-isopropyl-N4-(2-(trifluoromethyl)pyridin-4- -l,3 -triazine-2,4-diamine
Figure imgf000240_0003
1H NMR (DMSO-d6) δ 10.39-10.56 (m, 1H), 8.16-8.70 (m, 4H), 7.71-8.00 (m, 3H), 4.16-4.35 (m, 1H), 1.25 (dd, J = 6.4, 6H). LC-MS: m/z 427.1 (M+H)+.
Compound 648 - N2-isopropyl-6-( 2-methoxypyridin-3-yl)-N4-(2-( trifluoromethyl)pyridin-4-yl)- l,3,5-triazine-2,4-diamine
Figure imgf000241_0001
1H NMR (METHANOL-d4) δ 8.61-8.27 (m, 3 H), 8.23-7.88 (m, 2 H), 7.09-7.06 (m, 1 H), 4.28- 4.25 (m, 1 H), 4.01 (s, 3 H), 1.31-1.28 (m, 6 H). LC-MS: m/z 406.1 (M+H)+.
Example 9. Preparation of Compounds of Formula I Wherein Ring A is Substituted Aryl or Heteroaryl. The compounds of this Example are prepared by the general method in Scheme 9, set forth below.
Scheme 9
Figure imgf000241_0002
CCoommppoouunndd 664499 -- 66--((22--aammiinnooppyyrriimmiiddiinn--55--yyll))--NN22--((33,,55--ddiiflfluuoorroopphheennyyll))--NN44--iissoopprrooppyyll--ll,,33,,55-- ttrriiaazziinnee--22,,44--ddiiaammiinnee
Figure imgf000241_0003
Example 9, Step 1:
Preparation of 6-chloro-N2 -( 3,5-difluorophenyl)-N4-isopropyl-l,3,5-triazine-2,4-diamine
To a solution of 4,6-dichloro-N-isopropyl-l,3,5-triazin-2-amine (1 g, 4.83 mmol) in THF (10 mL) was added 3,5-difluoro aniline (0.62 g, 4.83 mmol), TiuONa (0.93 g, 9.66 mol) and Pd(dppf)Cl2 (0.35g, 0.48 mmol). The mixture was stiired at 80°C under N2 protection fro 2 hrs. The reaction was quenched by water and extracted by EtOAc. The organic layer was dried, concentrated and purified to afford 6-chloro-N2-(3,5-difluorophenyl)-N4-isopropyl- 1,3,5- triazine-2,4-diamine as white solid.
Example 9, Step 2:
To a mixture of 5-chloro-Nl-(3,5-difluorophenyl)-N3-isopropylbenzene-l,3-diamine (50 mg, 0.17 mmol), 5-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)pyrimidin-2-amine (37 mg, 0.17 mmol) and Cs2C03 (108 mg, 0.34 mmol) in dioxane/water (0.8 mL/0.16 mL) was added Pd(PPh3)4 (19 mg, 0.017 mmol). The mixture was heated to 80°C for 2 hours. The mixture was concentrated and purified by a standard method to give 6-(2-aminopyrimidin-5-yl)-N2-(3,5-difluoro-phenyl)-N4- isopropyl-l,3,5-triazine-2,4-diamine.
1H NMR (METHANOL-d4): δ 9.11-9.17 (m, 2H), 7.49-7.50 (m, 2H), 6.51-6.55 (m, IH), 4.22- 4.34 (m, IH), 1.35 (d, J = 6.8 Hz, 6H). LC-MS: m/z 359.2 (M+H)+.
The following compounds were prepared according Example 8, method B, using appropriate intermediates and reagents.
Compound 650 - 6-{4-(hopropylamino)-6-{{2-(trifluoromethyl)pyridin-4-yl)amm
-yl)pyridin-2( lH)-one
Figure imgf000242_0001
1H NMR (METHANOL-d4) δ 8.70-8.25 (m, 2H), 8.15-8.06 (m, IH), 7.81-7.50 (m, IH), 6.89 (br, IH), 4.31-4.23 (m, IH), 1.34-1.29 (m, 6H). LC-MS: m/z 392.1 (M+H)+.
Compound 651 - 6-(4-(isopropylamino)-6-((2-(trifluoromethyl)pyridin-4-yl)amino)-l,3,5-tria^ 2-yl)picolinamide
Figure imgf000242_0002
1H NMR (DMSO-d6) δ 10.56 (br, 1 H), 8.87-8.85 (m, IH), 8.68-8.04 (m, 6H), 7.92-7.96 (m, 7.63-7.59 (m, IH), 7.58-7.48 (m, IH), 4.20-4.15 (m, IH), 1.25 (d, 6H). LC-MS: m/z 418.2 (M+H)+.
Compound 652 - 2,2,2-trifluoro-l-(3-(4-(isopropylamino)-6-((2-(trifluoromethyl)pyridin-4- yl)amino)-l,3,5-triazin-2-yl)phenyl)ethanol
Figure imgf000243_0001
1H NMR (METHANOL-d4) δ 8.76-8.40 (m, 4H), 8.32-7.52 (m, 3H), 5.16-5.11 (m, 1H), 4.51-4.28 (m, 1H), 1.34 (d, 6H). LC-MS: m/z 473.2 (M+H)+.
Compound 653 - N-Isopropyl-6-(3-methanesulflnyl-phenyl)-N'-(2-trifluoromethyl-pyridin-4-yl)- [l,3,5]triazine-2,4-diamine
Figure imgf000243_0002
1H NMR (METHANOL-d4) δ 8.81-8.28 (m, 4H), 7.91-7.71 (m, 3H), 4.51-4.28 (m, 1H), 2.88 (s, 3H), 1.36-1.33 (m, 6 H). LC-MS: m/z 437.2 (M+H)+.
Compound 654 - 6-(3-(aminomethyl)phenyl)-N2 sopropyl-N4-(2-(trifluoromethyl)pyridin-4-yl)- -triazine-2,4-diamine
Figure imgf000243_0003
1H NMR (METHANOL-d4) δ 8.66-8.40 (m, 4H), 7.96 (br, 1H), 7.77-7.67 (m, 2H), 4.52-4.31 (m, 1H), 4.24 (s, 2H), 1.34 (d, 6H). LC-MS: m/z 404.2 (M+H)+.
Compound 655 - 6-(3-chloro-5-methoxyphenyl)-N2 sopropyl-N4-(2-(trifluoromethyl)pyridin-4- -l,3,5-triazine-2,4-diamine
Figure imgf000243_0004
1H NMR (DMSO-d6) δ 10.44 (d, 1H), 8.71 (s, 1H), 8.57-8.55 (m, 1H), 8.30-8.08 (m, 1H), 7.92- 7.79 (m, 3H), 6.97 (s, 1H), 4.35-4.13 (m, 1H), 3.86 (s, 3H), 1.24 (d, 6H). LC-MS: m/z 439.2 (M+H)+.
Compound 657 - N-Isopropyl-6-(3-methanesulfonyl-phenyl)-N'-(2-trifluoromethyl-pyridin-4-yl)- [l,3,5]triazine-2,4-diamine
Figure imgf000244_0001
1H NMR (METHANOL-d4) δ 8.95 (s, 1H), 8.76-7.98 (m, 5H), 7.80-7.76 (m, 1H), 4.49-4.22 (m, 1H), 3.17 (s, 3H), 1.34-1.27 (m, 6 H). LC-MS: m/z 453.2 (M+H)+.
Compound 658 - 3-Fluoro-5-[4-isopropylamino-6-(2-trifluoromethyl-pyridin-4-ylamino)- [l,3,5]triazin-2-yl]-phenol
Figure imgf000244_0002
1H NMR (METHANOL-d ) δ 8.63-8.63 (m, 2H), 7.95 (s, 1H), 7.56-7.49 (m, 2H), 6.80-6.78 (d, J= 8.8 Hz, 1H), 4.31 (s, 1H), 1.36-1.34 (d, J= 6 Hz, 6H). LC-MS: m/z 409.1 (M+H)+.
Compound 660 - 6-(3-fluoro-5-(trifluoromethyl)phenyl)-N2-isopropyl-N4-(3- (methylsulfonyl)phenyl)-l,3,5-triazine-2,4-diamine
Figure imgf000244_0003
1H NMR (Methanol-d4) δ 8.98 (s, 1H), 8.55 (s, 1H), 8.37 (d, 1H), 7.99-7.75 (m, 1H), 7.61-7.53 (m,
3H), 4.37-4.34 (m, 1H), 3.15 (d, 3H), 1.30 (d, 6H). LC-MS: m/z 470.0 (M+H)+.
Compound 662 - 6-(3-fluoro-5-methoxyphenyl)-N2 sopropyl-N4-(2-(trifluoromethyl)pyridin-4- yl)-l,3,5-triazine-2,4-diamine
Figure imgf000245_0001
1H NMR (DMSO-d6) δ 10.30 (d, 1H), 8.67-8.04 (m, 3H), 8.04-7.58 (m, 3H), 7.08-7.03 (m, 1H), 4.35-4.10 (m, 1H), 3.83 (s, 3H), 1.21 (d, 3H). LC-MS: m/z 423.2 (M+H)+.
Compound 663 - l-(3-(4-(isopropylamino)-6-((2-(trifluoromethyl)pyridin-4-yl)a
triazin-2-yl)phenyl)ethanol
Figure imgf000245_0002
1H NMR (METHANOL-d4) δ 8.74-8.29 (m, 4H), 8.28-7.80 (m, 1H), 7.57-7.43 (m, 2H), 4.48-4.26
(m, 1H), 1.49 (d, 3H), 1.31 (d, 6H). LC-MS: m/z 419.2 (M+H)+.
6-(3-(l-(( tert-butyldimethylsilyl)oxy )cyclopropyl)phenyl)-N2-isopropyl-N4-(2-
(trifluoromethyl)pyridin-4-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000245_0003
LCMS: m/z 545.3 (M+H)+.
Figure imgf000245_0004
To a solution of 6-(3-(l-((tert-butyldimethylsilyl)oxy)cyclopropyl) phenyl)-N2-isopropyl-N4- (2- (trifluoromethyl)pyridin-4-yl)-l,3,5-triazine-2,4-diamine (510 mg, 0.936 mmol) in anhydrous THF (15 mL) was TBAF (490 mg, 1.872 mmol) at room temperature. The mixture was stirred at r.t. for 2 hours. The mixture was partitioned between EtOAc and water. The organic layer was washed with brine, dried over Na2S04, then concentrated. The crude product was purified by a standard method to give l-(3-(4-(isopropylamino)-6-((2-(trifluoromethyl)pyridin -4-yl)amino)-l,3,5-triazin- 2-yl)phenyl)cyclopropanol.
Compound 664 - l-(3-(4-(isopropylamino)-6-((2-(trifluoromethyl)pyridin-4-yl)amino)-l,3,5- triazin-2-yl)phenyl)cyclopropanol
Figure imgf000246_0001
1H NMR (METHANOL-d4) δ 8.67-8.46 (m, 2H), 8.31-8.21 (m, 2H), 7.84-7.83 (m, IH), 7.52-7.39 (m, 2H), 4.45-4.23 (m, IH), 1.32-1.30 (d, J = 8.0 Hz, 6H), 1.23-1.22 (m, 2H), 1.09-1.06 (m, 2H). LC-MS : m/z 431.2 (M+H)+.
Compound 665 - 3-(hydroxymethyl)-5-(4-(isopropylamino)-6-((2-(trifluoromethyl)pyridin-4- yl)amino)-l,3,5-triazin-2-yl)phenol
Figure imgf000246_0002
1H NMR (CDC13) δ 10.40-10.24 (m, IH), 9.56 (s, IH), 8.68-8.26 (m, 2H), Ί .93-1.59 (m, 3H), 6.94 (s, IH), 5.23-5.20 (m, IH), 4.50-4.49 (d, J=5.6, 2H), 4.20-4.12 (m, IH) 1.26-1.23 (m, 6H). LC- MS : m/z 421.2 (M+H)+.
The following compounds were prepared according to Scheme 5 using appropriate intermediates and reagents:
Compound 667 - 4-(4-Phenyl-6-phenylamino-[l,3,5]triazin-2-ylamino)-piperidine-l-carboxylic acid tert-butyl ester
Figure imgf000246_0003
1H NMR (CDC13) δ: 8.23-8.82 (m, 2H), 8.53-7.66 (m., 2H), 7.33-7.48 (m, 3H), 7.25-7.31 (m, 2H), 6.98-7.09 (m., 2H), 5.05-5.29 (m, 1H), 3.95-4.20 (m, 3H), 2.85-2.97 (m, 2H), 2.03 (d, J = 12 Hz, 2H), 1.37-1.42 (m, 11H). LC-MS: m/z 447.0 (M+H)+.
Example 10: Preparation of compounds of Formula 1 via N-arylation of triazine-amine cross-coupling.
Scheme 10
(Ring B)-halide
Pd2(dba)3, BINAP, Cs2C03
toluene, 1 10°C, 30min, MW
Figure imgf000247_0001
R3 = Aryl or heteroaryl
Example 10, Step 1: Preparation of N2-isopropyl-6-(6-(trifluoromethyl)pyridin-2-yl)-l,3,5- triazine-2,4-diamine. To the solution of 4-chloro-N-isopropyl-6-(6-(trifluoromethyl)pyridin-2- yl)-l,3,5-triazin-2-amine (300 mg, 0.94 mmol) in THF (5mL) was added NH3/H20 (8 mL). The mixture was stirred at 80°C overnight. TLC (PE: EA = 1: 1) showed the reaction was complete. The mixture was washed with H20 and ethyl acetate. The organic layer was dried over Na2S04, filtered , concentrated to give N2-isopropyl-6-(6-(trifluoromethyl)pyridin-2-yl)-l,3,5-triazine-2,4- diamine as a yellow solid which was used without further purification. LC-MS : m/z 299.8 (M+H)+.
The following intermediates were prepared using the procedure in Example 10, Step 1:
-/ 6-( l,l-Difluoro-ethyl)-pyridin-2-yl]- N-isopropyl-[l,3,5]triazine -2,4-diamine
Figure imgf000247_0002
LC-MS : m/z 295.2 (M+H)+.
6-(6-Difluoromethyl-pyridin-2-yl)-N -isopropyl-[l,3,5]triazine-2,4-diamine
Figure imgf000248_0001
LC-MS : m/z 281.1 (M+H)+.
l-(4-amino-6-(6-(trifluoromethyl) pyridin-2-yl)-l,3,5-triazin-2-ylamino)-2-methylpropan-2-ol
Figure imgf000248_0002
LC-MS : m/z 329.0 (M+H)+.
Step 2: Preparation of l-(4-(4-(isopropylamino)-6-(6-(trifluoromethyl)pyridin-2-yl)-l,3,5- triazin-2-ylamino)pyridin-2-yl)cyclopropanecarbonitrile. To a solution of N2-isopropyl-6-(6- (trifluoromethyl)pyridin-2-yl)-l,3,5-triazine-2,4-diamine (120 mg, 0.4 mmol) in anhydrous toluene (5 mL) was added l-(4-chloro-pyridin-2-yl)cyclopropanecarbonitrile (89 mg, 0.48 mmol), Cs2C03 (262 mg, 0.8 mmol), BINAP (24.9 mg, 0.04 mmol), and Pd2(dba)3 (36.6 mg, 0.04 mmol) under N2. The mixture was stirred at 110°C for 30 min under M.W. irradiation. The mixture was quenched by water and extracted with ethyl acetate. The organic layer was dried with anhydrous Na2S04, concentrated and purified by a standard method to give l-(4-(4-(isopropylamino)-6-(6- (Mfluoromethyl)-pyridin-2-yl)-l,3,5-triazin-2-ylamino)pyridin-2-yl)cyclop
The following compounds were prepared from the appropriate intermediates using the procedure in Example 10, Step 2:
Compound 669 - l-{4-[4-Isopropylamino-6-(6 rifluoromethyl-pyridin-2-yl)-[l,3,5]triazin-2- ylamino]-pyridin-2-yl}-cyclopropanecarbonitrile
Figure imgf000248_0003
1H NMR (METHANOL-d4) δ 8.79-8.78 (m, 2H), 8.27(d, J = 5.6 Hz, IH), 8.20 (t, J = 8.2 Hz, IH), 7.36 (dd, J = 3.6 Hz, 2.0 Hz, IH), 4.47 (m, IH), 1.82-1.73 (m, 4H), 1.31 (d, J = 4.0 Hz, 6H). LC- MS: m/z 441.2 (M+H)+.
Compound 670 -l-[4-(5-Chloro-6-fluoro-pyridin-3-ylamino)-6-(6 rifluoromethyl-pyridin-2-yl)- [l,3,5]triazin-2-ylamino]-2-methyl-propan-2-ol
Using the standard procedure described in except replacing BINAP with X-Phos and CS2CO3 with -BuONa to give 670.
Figure imgf000249_0001
1H NMR (METHANOL-d ) δ 8.82-8.63 (m, 2H), 8.39-8.38 (m, IH), 8.22 (t, J= 7.9 Hz, IH), 7.98 (d, J = 7.6 Hz, IH), 3.63 (s, IH), 3.55 (s, IH), 1.30 (d, J= 4.0 Hz, 6H). LC-MS: m/z 458.2
(M+H)+.
Compound 671 - 2-{4-[4-Isopropylamino-6-(6-trifluoromethyl-pyridin-2-yl)-[l,3,5]triazin-2- ylamino]-pyridin-2-yl}-2-methyl-propionitrile
Figure imgf000249_0002
1H NMR (METHANOL-d ) δ 8.77-8.73 (m, IH), 8.50 (s, IH), 8.40 (d, J = 4.4 Hz, IH), 8.23 (t, J = 6.6 Hz, IH), 8.00 (d, J = 8.0 Hz, IH), 7.57 (dd, J = 3.6 Hz, 2.0 Hz, IH), 4.49-4.41 (m, IH), 1.74 (s, 6H), 1.34 (d, J = 6.4 Hz, 6H). LC-MS: m/z 443.2 (M+H)+.
Compound 672 - {4-[4-Isopropylamino-6-(6-trifluoromethyl-pyridin-2-yl)-[l,3,5]triazin-2- ylamino]-pyridin-2-yl}-acetonitrile
Figure imgf000249_0003
1H NMR (METHANOL-d4) δ 10.41 (s, IH), 8.62 (dd, J = 9.6 Hz, 8.0 Hz, IH), 8.37 (d, J = 2.4 Hz, IH), 8.29 (dd, J = 8.4 Hz, 1.9 Hz„ 2H), 8.28 (s, IH), 8.11 (d, J = 7.6Hz, IH), 7.97-7.67 (m, IH), 4.35-4.28 (m, IH), 4.17 (s, IH), 4.13 (s, IH), 1.25 (d, J = 6.8 Hz, 6H). LC-MS: m/z 415.3 (M+H)+.
Compound 673 - 6-(6-Difluoromethyl-pyridin-2-yl)-N-(2-difluoromethyl-pyridin-4-yl)-N'- isopropyl-[l,3,5]triazine-2,4-diamine
Using the standard procedure described in Example 10 Step 2 except replacing CS2CO3 by t- BuONa yielded 673.
Figure imgf000250_0001
1H NMR (METHANOL-d4) δ 8.64-7.77 (m, 6H), 6.98-6.58 (m, 2H), 4.33-4.30 (m, IH), 1.34 (d, J = 6.4 Hz, 6H). LC-MS: m/z 408.2 (M+H)+.
Compound 674 - l-{4-[4-Isopropylamino-6-(6-trifluoromethyl-pyridin-2-yl)-[l,3,5]triazin-2- ylamino]-pyridin-2-yl}-cyclopropanol
Figure imgf000250_0002
1H NMR (METHANOL-d4) δ 8.61-8.64 (q, J = 7.6 Hz, 1 H), 8.38 (s, 1 H), 8.09-8.16 (m, 2 H), 7.86-7.88 (d, J = 7.6 Hz, 1 H), 7.44-7.62 (m, 1 H), 4.26-4.30 (m, 1 H), 1.76-1.23 (m, 8 H), 1.10- 1.12 (q, J = 4 Hz, 2 H). LC-MS: m/z 432.2 (M+H)+.
Compound 675 - 6-[6-(l,l-Difluoro-ethyl)-pyridin-2-yl]-N-(2-difluoromethyl-pyridin-4-yl)- N'-isopropyl-[l,3,5]triazine-2,4-diamine
Using the standard procedure described in Example 10 Step 2 except replacing CS2CO3 by t- BuONa yielded 675.
Figure imgf000250_0003
1H NMR (METHANOL-d4) δ 8.58-8.46 (m, 2H), 8.18-8.11 (m, 2H), 7.90-7.88 (m, 2H), 6.86-6.58 (m, 1H), 4.34-4.32 (m, 1H), 2.17-2.05 (m, 3H), 1.35 (d, J = 7.2 Hz, 6H). LC-MS: m/z 422.2 (M+H)+.
Compound 676 - N-(2-Fluoromethyl-pyridin-4-yl)-N'-isopropyl-6-( 6-trifluoromethyl-pyridin-2- yl)-[l,3,5]triazine-2,4-diamine
Using the standard procedure described in Example 10 Step 2 except replacing CS2CO3 by t- BuONa yielded 676.
Figure imgf000251_0001
1H NMR (METHANOL-d4) δ 8.72-8.70 (m, 1H), 8.40-7.98 (m, 5H), 5.55 (s, 1H), 5.43 (s, 1H), 4.52-4.33 (m, 1H), 1.34 (d, J = 8.4 Hz, 6H). LC-MS: m/z 408.1 (M+H)+.
Compound 677 - 2-(4-{4-[6-(l,l-Difluoro-ethyl)-pyridin-2-yl]-6 sopropylamino-[l,3,5]triazin-2- ylamino}-pyridin-2-yl)-2-methyl-propionitrile
Figure imgf000251_0002
1H NMR (METHANOL-d ) δ 8.61 (d, J = 6.8 Hz, 1H) , 8.45 (s, 1H), 8.40 (d, J = 5.2 Hz, 1H), 8.11 (t, J = 7.6 Hz, 1H), 7.88 (d, J = 8.0 Hz, 1H), 7.62 (s, 1H), 2.12 (t, J = 19.2 Hz, 3H), 1.13 (d, J = 6.4 Hz, 6H). LC-MS: m/z 439.2(M+H)+.
Compound 678 - 2-{4-[4-(2-Hydroxy-2-methyl-propylamino)-6-(6-trifluoromethyl-pyridin-2-yl)- [l,3,5]triazin-2-ylamino]-pyridin-2-yl}-2-methyl-propionitrile
Figure imgf000251_0003
1H NMR (METHANOL-d ) δ 8.80-8.78 (m, 1H), 8.45 (s, 1H), 8.40 (t, J = 5.6 Hz, 1H), 8.22 (t, J = 7.8 Hz, 1H), 8.79 (d, J = 8.0 Hz, 1H), 7.60 (dd, J = 3.6 Hz, 2.0 Hz, 1H), 3.63 (d, J = 11.6 Hz, 2H), 1.80 (s, 6H), 1.31 (d, J = 6.0 Hz, 6H). LC-MS: m/z 473.2(M+H)+. Example 11: Preparation of compounds of Formula I where Ring A is 6-aminopyridyl.
Scheme 11
Figure imgf000252_0001
Example 11, Step 1: The preparations of the following intermediates are analogous to the procedure as Scheme 3, Step 4, using the appropriate starting materials and intermediates:
Compound 679 - Methyl (6-(4-(isopropylamino)-6-((2-(trifluoromethyl)pyridin-4-yl)amino)- -triazin-2-yl)pyridin-2-yl)carbamate
Figure imgf000252_0002
LCMS: m/z 449.3 (M+H)+.
Compound 680 - Methyl 6-{4-(2-hydroxy-2-methyl- propylamino)-6-(2-(trifluoromethyl)pyridin- -ylamino)-l,3,5-triazin-2-yl)pyridin-2-yl-carbamate
Figure imgf000252_0003
LCMS: m/z 479.3 (M+H)+.
Compound 681 - Methyl 6-(4-(neopentylamino)-6-(2-(trifluoromethyl)pyridin-4-ylamino)-l,3,5- triazin-2-yl)pyridin-2-ylcarbamate
Figure imgf000253_0001
LCMS: m/z 477.3 (M+H)+.
Compound 682 - Methyl 6-(4-(3,5-difluorophenylamino)-6-(l-methylcyclopropylamino)-l,3,5- triazin-2-yl)pyridin-2-ylcarbamate
Figure imgf000253_0002
LCMS: m/z 428.2 (M+H)+.
Methyl 6-( 4-( 1-methylcyclopropylamino )-6-( 2-( trifluoromethyl)pyridin-4-ylamino )-l,3,5-triazin- -yl)pyridin-2-ylcarbamate
Figure imgf000253_0003
LCMS: m/z 461.3 (M+H)+.
Compound 683 - Methyl 6-(4-(2-(trifluoromethyl)pyridin-4-ylamino)-6- (1,1,1-trifluoro- propan- -ylamino)-l,3,5-triazin-2-yl)pyridin-2-ylcarbamate
Figure imgf000253_0004
LCMS: m/z 503.2 (M+H)+.
Compound 684 - Methyl 6-(4-(3,5-difluorophenylamino)-6-(2-hydroxy-2- methylpropyl- amino)- l,3,5-triazin-2-yl)pyridin-2-ylcarbamate
Figure imgf000254_0001
LCMS: m/z 446.1 (M+H)+.
Preparation of methyl 6-(4-(tert-butylamino)-6-(2-(trifluoromethyl)pyridin-4-ylamino)- 1, triazin-2-yl)pyridin-2-ylcarbamate
Using the standard procedure described above to give Compound 685 - methyl 6-(4-(tert- butylamino)-6- (2-(trifluoromethyl)pyridin-4-ylamino)- l,3,5-triazin-2-yl) pyridin-2- ylcarbamate
Figure imgf000254_0002
LCMS: m/z 463.3 (M+H)+.
Compound 686 - Methyl 6-(4-(2-(l,l-difluoroethyl)pyridin-4-ylamino)-6- (isopropyl- amino)- -triazin-2-yl)pyridin-2-ylcarbamate
Figure imgf000254_0003
LCMS: m/z 445.1 (M+H)+.
Example 11, Step 2: Preparation of 6-(6-aminopyridin-2-yl)-N2-isopropyl-N4-(2- ( trifluoromethyl)pyridin-4-yl)-l, 3,5-triazine-2,4-diamine.
To a solution of 6-(6-Chloro-pyridin-2-yl)-N-oxetan- 3-yl-N'-(2-trifluoromethyl- pyridin-4-yl)- [l,3,5]triazine-2,4-diamine (170 mg, 0.38 mmol) in methanol (6mL) was added 5 pellets of KOH. The mixture was heated to 80°C for 12 hours. TLC (ethyl acetate) showed that the reaction was complete. The mixture was adjusted pH to 7 and filtered, the filtrate was concentrated and purified by a standard method to give 6-(6-aminopyridin-2-yl)-N2-isopropyl-N4-(2- (trifluoromethyl)pyridin-4-yl)-l,3,5-triazine-2,4-diamine.
The following compounds were prepared according to the procedure set forth in Example 11, Step 2, using appropriate starting materials and reagents:
Compound 687 - 6-(6-aminopyridin-2-yl)-N2 sopropyl-N4-(2-(trifluoromethyl)pyridin-4-yl)- -triazine-2,4-diamine
Figure imgf000255_0001
1H NMR (METHANOL-d4): δ 8.5-8.65 (m, 1.5 H), 7.8-8.3 (m, 3.5 H), 7.2 (m, 1 H), 4.2-4.6 (m, 1 H), 1.25-1.4 (m, 6 H). LC-MS: m/z 391.3 (M+H)+.
Compound 689 - 6-(6-aminopyridin-2-yl)-N2-neopentyl-N4-(2-(trifluoromethyl)pyridin-4-yl)- -triazine-2,4-diamine
Figure imgf000255_0002
1H NMR (METHANOL-d ) : δ 8.75 (m, 1 H), 8.1-8.6 (m, 2 H), 7.6-7.8 (m, 2 H), 6.85 (m, 1 H), 3.4-3.5 (m, 2 H), 1.0 (s, 9 H). LC-MS: m/z 419.3 (M+H)+.
Compound 690 - 6-(6-aminopyridin-2-yl)-N2-isobutyl-N4-(2-(trifluoromethyl)pyridin-4-yl)- -triazine-2,4-diamine
Figure imgf000255_0003
Compound 691 - l-(4-(6-aminopyridin-2-yl)-6-(3,5-difluorophenylamino)-l,3,5-triazin-2- ylamino )-2-methylpropan-2-ol
Figure imgf000256_0001
IH NMR (METH ANOL-d4) : δ 8.6-7.6 (m, 3 H), 7.55-6.5 (m, 3 H), 3.5-3.7 (m, 2 H), 1.1-1.4 (m, 6 H). LC-MS: m/z 338.2 (M+H)+.
Compound 692 - 6-(6-aminopyridin-2-yl)-N2-(l-methylcyclopropyl)-N4-(2- (trifluoromethyl)pyridin-4-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000256_0002
IH NMR (METH ANOL-d ) : δ 8.88 (m, 1 H), 8.5 (m, 1 H), 7.85 (m, 1 H), 7.7 (m, 1 H), 7.6 (m, 1 H), 6.75 (m, 1 H), 1.52 (s, 3 H), 0.75-0.95 (m, 4 H). LC-MS: m/z 403.2 (M+H)+.
Compound 693 - 6-(6-aminopyridin-2-yl)-N2-(3,5-difluorophenyl)-N4-(l-methylcyclopropyl)- l,3,5-triazine-2,4-diamine
Figure imgf000256_0003
IH NMR (METH ANOL-d4) : δ 7.5-7.58 (m, 4 H), 6.5-6.8 (m, 2 H), 1.5 (s, 3 H), 0.75-0.95 (m, 4 H). LC-MS: m/z 370.2 (M+H)+.
Compound 694 - 6-(6-aminopyridin-2-yl)-N2-(2-(trifluoromethyl)pyridin-4-yl)-N4-(l,l,l- trifluoropropan-2-yl)-l,3,5-triazine-2,4-diamine
Figure imgf000256_0004
1H NMR (METHANOL-d4) : δ 78.63-7.75 (m, 4 H), 7.6 (m, 1 H), 6.68 (m, 1 H), 5.5-5.0 (m, 1 H), 1.48 (m, 3 H). LC-MS: m/z 445.2 (M+H)+. Compound 695 - 6-(6-aminopyridin-2-yl)-N2-tert-butyl-N4-(2-(tnfluoromethyl)pyridin-4-yl)- l,3,5-triazine-2,4-diamine
Figure imgf000257_0001
1H NMR (METHANOL-d4): δ 8.55-8.65 (m, 2 H), 7.9-8.25 (m, 2 H), 7.8-7.9 (m, 1 H), 7.2 (m, 1 H), 1.55 (m, 9 H). LC-MS: m/z 405.2 (M+H)+.
Compound 696 - 6-( 6-aminopyridin-2-yl)-N2-(2-( l,l-difluoroethyl)pyridin-4-yl)-N4-isopropyl- -triazine-2,4-diamine
Figure imgf000257_0002
1H NMR (METHANOL-d4): δ 8.55-8.2 (m, 2 H), 8.0-7.55 (m, 3 H), 6.75 (m, 1 H), 4.55-4.2 (m, 1 H), 2.0 (t, 3 H), 1.3 (d, J = 6.4 Hz, 3 H). LC-MS: m/z 387.3 (M+H)+.
Compound 697 - N-(6-(4-(isopropylamino)-6-(2-(trifluoromethyl)pyridin-4-ylamino)-l,3,5- triazin-2- l ridin-2-yl)acetamide
Figure imgf000257_0003
1H NMR (METHANOL-d ) : δ 8.7-8.5 (m, 2 H), 8.3-7.8 (m, 4 H), 4.5-4.2 (m, 1 H), 2.23 (s, 3 H), 1.25-1.35 (m, 6 H). LC-MS: m/z 433.2 (M+H)+.
Compound 698 - 6-(6-aminopyridin-2-yl)-N2-(tert-butyl)-N4-(3,5-difluorophenyl)-l,3,5-triazine- 2,4-diamine
Figure imgf000257_0004
1H NMR (METH ANOL-d4) : δ 7.68-7.48 (m, 4 H), 6.73-6.55 (m, 2 H), 1.58 (s, 9 H). LC-MS: m/z 372.2 (M+H)+.
Compound 699 - 6-(6-aminopyridin-2-yl)-N2-(cyclopropylmethyl)-N4-(3,5-difluorophenyl)- -triazine-2,4-diamine
Figure imgf000258_0001
1H NMR (METHANOL-d4): δ 7.71-7.50 (m, 4 H), 6.74-6.72 (m, 1 H), 6.56-6.54 (m, 1 H), 3.43- 3.36 (m, 2 H), 1.18-1.72 (m, 1 H), 0.56-0.54 (m, 2 H), 0.32-0.31 (m, 2 H). LC-MS: m/z 370.1 (M+H)+.
Example 12. Enzymatic and Cell Assays.
Enzymatic Assay. Compounds are assayed for IDH2 R172K inhibitory activity through a cofactor depletion assay. Compounds are preincubated with enzyme, then the reaction is started by the addition of NADPH and a- KG, and allowed to proceed for 60 minutes under conditions previously demonstrated to be linear with respect for time for consumption of both cofactor and substrate. The reaction is terminated by the addition of a second enzyme, diaphorase, and a corresponding substrate, resazurin. Diaphorase reduces resazurin to the highly fluorescent resorufin with the concomitant oxidation of NADPH to NADP, both halting the IDH2 reaction by depleting the available cofactor pool and facilitating quantitation of the amount of cofactor remaining after a specific time period through quantitative production of an easily detected fluorophore.
Specifically, into each of 12 wells of a 384- well plate, 1 μΐ of lOOx compound dilution series is placed, followed by the addition of 40 μΐ of buffer (50 mM potassium phosphate
(K2HP04), pH 7.5; 150 mM NaCl; 10 mM MgCl2, 10% glycerol, 0.05% bovine serum albumin, 2 mM beta-mercaptoethanol) containing 1.25 μg/ml IDH2 R172K. The test compound is then incubated for one hour at room temperature with the enzyme; before starting the IDH2 reaction with the addition of 10 μΐ of substrate mix containing 50 μΜ NADPH and 6.3 mM a- KG in the buffer described above. After a further one hour of incubation at room temperature, the reaction is halted and the remaining NADPH measured through conversion of resazurin to resorufin by the addition of 25 μΐ Stop Mix (36 μg/ml diaphorase enzyme and 60 μΜ resazurin; in buffer). After one minute of incubation the plate is read on a plate reader at Ex544/Em590.
For determination of the inhibitory potency of compounds against IDH2 R140Q in an assay format similar to the above, a similar procedure is performed, except that the final testing concentration is 0.25 μ^πύ IDH2 R140Q protein, 4 μΜ NADPH and 1.6 mM a-KG.
For determination of the inhibitory potency of compounds against IDH2 R140Q in a high throughput screening format, a similar procedure is performed, except that 0.25 μg/ml IDH2 R140Q protein was utilized in the preincubation step, and the reaction is started with the addition of 4 μΜ NADPH and 8 μΜ α-KG.
U87MG pLVX-IDH2 R140Q-neo Cell Based Assay. U87MG pLVX-IDH2 R140Q-neo cells are grown in T125 flasks in DMEM containing 10% FBS, lx penicillin/streptomycin and 500 μg/mL G418. They are harvested by trypsin and seeded into 96 well white bottom plates at a density of 5000 cell/well in 100 μΐ/well in DMEM with 10% FBS. No cells are plated in columns 1 and 12. Cells are incubated overnight at 37°C in 5% C02. The next day compounds are made up at 2x concentration and lOOul are added to each cell well. The final concentration of DMSO is 0.2% and the DMSO control wells are plated in row G. The plates are then placed in the incubator for 48 hours. At 48 hours, lOOul of media is removed from each well and analyzed by LC-MS for 2-HG concentrations. The cell plate is placed back in the incubator for another 24 hours. At 72 hours post compound addition, 10 mL/plate of Promega Cell Titer Glo reagent is thawed and mixed. The cell plate is removed from the incubator and allowed to equilibrate to room
temperature. Then lOOul of reagent is added to each well of media. The cell plate is then placed on an orbital shaker for 10 minutes and then allowed to sit at room temperature for 20 minutes. The plate is then read for luminescence with an integration time of 500ms to determine compound effects on growth inhibition.
The data for various compounds of one aspect of the invention in the R140Q enzymatic assay, R140Q cell-based assay and R172K enzymatic assay as described above or similar thereto are presented below in Table 2. For each assay, values indicated as "A" represent an IC50 of less than 100 nM; values indicated as "B" represent an IC50 of between 100 nM and 1 μΜ; values indicated as "C" represent an IC50 of greater than 1 μΜ to 10 μΜ; values indicated as "D" represent an IC50 of greater than 10 μΜ; values indicated as "no fit" are inactives and blank values represent that the compound was either inactive or not tested in that particular assay. Table 2. Enzymatic and Cellular Activity of Compounds.
Cmpd Enz Cell Enz Cmpd Enz Cell Enz
No R140Q R140Q R172K No R140Q R140Q R172]
100 A A A 155 B No Fit D
103 B C C 156 B B C
108 B 158 A B B
109 B C C 159 B B C
110 A A B 160 A B B
111 A A A 162 B C C
112 A B B 165 B C
113 A A B 167 A A B
114 B C C 168 A A B
115 A B B 169 A B B
116 B C 170 B C B
117 B C 172 A B B
118 A B B 173 A A A
119 B C D 174 A A B
120 A A B 175 A A B
121 A A A 176 A B B
122 B C C 177 A A B
123 A B B 178 A A A
126 A A B 179 A A A
128 B C C 181 A A B
129 A B C 182 B
130 A A B 183 A A B
132 A A B 184 A B C
133 B D 185 A B B
135 B C D 186 A A B
137 B C 187 A A B
139 A B C 188 A A B
140 A B C 189 A B C
141 A B B 190 A A B
143 A B B 191 A A B
145 B C D 193 A A B
146 A A B 194 A A A
147 B B C 195 A A B
148 B B C 196 A A B
149 A A A 197 A A B
150 B B C 198 A A B
151 B B B 199 A A A
154 A B C 200 A A B Cmpd Enz Cell Enz Cmpd Enz Cell Enz
No R140Q R140Q R172K No R140Q R140Q R172K
201 A B C 244 B C B
202 A A A 245 A B B
203 A B C 246 B A B
204 A B C 247 A A A
205 A A B 248 A B C
206 A B B 249 A B B
207 B 250 A B B
208 A B B 251 B
209 A B B 252 B C
210 A A B 253 A A B
211 A B B 254 A B B
212 A A B 255 A A B
213 A A B 256 C
214 A B B 257 A B B
215 A B C 258 C
216 A B B 259 B B D
217 A C 260 A A A
218 A B C 261 A A B
219 A A B 262 B B C
220 A A B 263 A B C
221 B B C 264 C
222 B 265 B C
223 A A A 266 A B C
224 A B B 267 A B C
225 A B C 268 A B B
226 A B B 269 A A B
227 A A B 270 A B B
228 A B B 271 No Fit
229 A A A 272 B B
230 B B B 273 D
231 B 274 D
232 A B B 275 B B
233 A A B 276 B
234 No Fit 277 A B
235 B B C 278 No Fit
236 B B C 279 D
237 B B C 280 D
238 B B C 281 A B
239 A A B 282 No Fit
240 A B C 283 No Fit
241 A B C 284 B B
242 B B C 285 C
243 B C 286 D Cmpd Enz Cell Enz Cmpd Enz Cell Enz
No R140Q R140Q R172K No R140Q R140Q R172K
287 B 331 B A
288 A A 332 D No Fit
289 A B 334 B A A
290 B A 335 B A A
291 No Fit No Fit 336 B A B
292 No Fit No Fit 337 B B C
293 A A 340 A A A
294 No Fit No Fit 341 A A B
295 A A 342 B C C
296 B A 343 B B
297 A A 344 B A A
298 A A 345 B B B
299 A B 346 A B
300 B B 347 B
301 B A 348 D
302 A B 350 B B C
303 C No Fit 351 A B
304 C No Fit 352 A A
305 D No Fit 353 B A
306 B A 354 B A
308 A B 355 B A
309 A A 356 B A
310 B A 358 B A B
311 B B 359 B B
312 B C 360 B B
313 A A 361 B B
314 C No Fit 362 B B
315 A A 363 B A
316 B B 364 C B
317 A A 365 C
318 A A 366 B A
319 B A 367 B A
320 A A 368 C A
321 A A 369 A A
322 B A 370 A A
323 B A 371 A A
324 B C 372 A A A
325 A A 374 A A A
326 B A 376 B A
327 B B 377 B A
328 A A 378 B A
329 A A 379 B A
330 B A 380 B B Cmpd Enz Cell Enz Cmpd Enz Cell Enz
No R140Q R140Q R172K No R140Q R140Q R172K
381 B A 459 A A A
382 B A 460 A A A
383 B A 461 A A A
384 B A 462 B B B
385 C B 463 B A A
386 B A A 464 B A A
387 A A 465 B A A
388 C B 466 B A B
389 C A 467 B B B
390 C B 468 B A A
391 B A 469 A A A
392 B A 470 B A B
393 B A 471 B A B
394 A A 472 A A B
395 B A 473 A A A
396 B A 474 B A A
397 B B 475 A A A
398 A A 476 A A B
399 B A 477 B A A
400 B A 478 B A A
401 B A 479 B A B
402 B A 480 B A B
403 B A 481 B A A
404 B A 482 B A A
405 C B 483 B B C
406 B A 484 B A B
407 B B 485 B A B
408 B A 486 B B
409 B A B 491 B A A
410 D B 492 B A A
411 C A 493 A A
412 C 495 B A A
413 D 496 B A A
414 B B 497 B A B
415 D 498 B B C
416 A A B 499 B A A
450 B A 500 B A A
451 B A 501 B B C
452 B C D 502 B B C
454 B B C 503 C A A
455 B A A 504 B A A
456 B A B 505 B A B
458 B A B 508 B A B Cmpd Enz Cell Enz Cmpd Enz Cell Enz
No R140Q R140Q R172K No R140Q R140Q R172K
509 B A B 559 B A A
510 B A A 560 B A A
511 B A B 561 B A A
512 B A B 562 B A A
513 C A B 563 B A A
514 B A A 564 B A A
516 B A A 565 B A A
517 B A A 567 B A A
518 B A A 568 B A B
519 B A B 569 B B B
521 B A A 570 B A A
522 B A B 571 B A B
523 B A A 572 B A B
524 B A A 574 B A A
526 B A A 576 B A B
527 B A A 577 C A B
528 B A B 581 B A A
529 B A A 582 B A A
530 B A B 583 B A A
531 B A A 584 B A A
532 B A A 585 B A A
533 B A A 587 B A A
534 B A A 588 B A B
535 B A B 592 B A B
536 C A B 593 B A A
537 B A A 594 B A B
538 C A B 595 B A A
540 B A B 596 B A A
541 B A B 597 B A A
542 B A A 598 B A A
543 B A B 599 B A A
544 B A B 600 B A A
545 B A B 601 B A A
546 B A B 602 B A A
547 B A A 603 B A A
548 B A B 604 B A A
549 B A A 605 B A B
550 B A A 606 B A A
551 B A A 607 B A B
552 B A B 608 B A A
554 B A B 609 B A A
555 B A C 610 B A A
556 B A A 611 B A B Cmpd Enz Cell Enz Cmpd Enz Cell Enz
No R140Q R140Q R172K No R140Q R140Q R172]
612 B A A 650 B B C
613 B A A 651 B A B
614 B A A 652 B B B
615 B A B 653 B A B
616 B A A 654 B A D
617 B A A 655 B B B
618 B A A 657 B A B
619 B A A 658 B A A
621 B B C 660 B C
622 B B B 662 B C
623 B B C 663 A A
624 B A B 665 A A
625 A A B 667 B B B
626 B B C 669 B A A
627 A A A 670 B A B
628 A A B 671 B A A
629 A A A 672 B A B
630 A A A 673 B A A
631 A A A 674 B A B
632 B A B 675 B A A
633 B A A 676 B A A
634 B A A 677 B A A
635 B B B 678 C A B
636 A A B 679 B B D
637 B A B 687 B A A
638 B A B 689 B A A
639 B A A 690 B A A
640 A A A 691 B A B
641 B A A 692 B A A
642 B A A 693 B A A
644 B C 694 B A A
645 B A B 695 B A A
646 B A A 696 B A B
647 B A B 697 B B C
648 B A B 698 B A A
649 A B B 699 B A A
In some embodiments, one aspect of the invention provides a compound selected from any one of Compounds Nos 100, 110, 111, 112, 113, 115, 118, 120, 121, 123, 126, 129, 130,
132, 139, 140, 141, 143, 146, 149, 154, 158, 160, 167, 168, 169, 172, 173, 174, 175, 176, 177,
178, 179, 181, 183, 184, 185, 186, 187, 188, 189, 190, 191, 193, 194, 195, 196, 197, 198, 199, 200, 201, 202, 203, 204, 205, 206, 208, 209, 210, 211, 212, 213, 214, 215, 216, 217, 218, 219, 220, 223, 224, 225, 226, 227, 228, 229, 232, 233, 239, 240, 241, 245, 246, 247, 248, 249, 250, 253, 254, 255, 257, 260, 261, 263, 266, 267, 268, 269, 270, 277, 281, 288, 289, 290, 293, 295, 296, 297, 298, 299, 301, 302, 306, 308, 309, 310, 313, 315, 317, 318, 319, 320, 321, 322, 323, 325, 326, 328, 329, 330, 331, 334, 335, 336, 340, 341, 344, 346, 351, 352, 353, 354, 355, 356, 358, 363, 366, 367, 369, 370, 371, 372, 374, 376, 377, 378, 379, 381, 382, 383, 384, 386, 387,
391, 392, 393, 394, 395, 396, 398, 399, 400, 401, 402, 403, 404, 406, 408, 409, 416, 450, 455, 456, 458, 459, 460, 461, 463, 464, 465, 466, 468, 469, 470, 471, 472, 473, 474, 475, 476, 477, 478, 479, 480, 481, 482, 484, 485, 491, 492, 493, 495, 496, 497, 499, 500, 504, 505, 508, 509, 510, 511, 512, 514, 516, 517, 518, 519, 521, 522, 523, 524, 526, 527, 528, 529, 530, 531, 532, 533, 534, 535, 537, 540, 541, 542, 543, 544, 545, 546, 547, 548, 549, 550, 551, 552, 554, 555, 556, 559, 560, 561, 562, 563, 564, 565, 567, 568, 570, 571, 572, 574, 576, 581, 582, 583, 584, 585, 587, 588, 592, 593, 594, 595, 596, 597, 598, 599, 600, 601, 602, 603, 604, 605, 606, 607, 608, 609, 610, 611, 612, 613, 614, 615, 616, 617, 618, 619, 624, 625, 627, 628, 629, 630, 631, 632, 633, 634, 636, 637, 638, 639, 640, 641, 642, 645, 646, 647, 648, 649, 651, 653, 654, 657, 658, 663, 665, 669, 670, 671, 672, 673, 674, 675, 676, 677, 687, 689, 690, 691, 692, 693, 694, 695, 696, 698 and 699. In a more specific aspect of this embodiment, the invention provides a compound selected from any one of Compound Nos.100, 110, 111, 113, 120, 121, 126, 130, 132, 146, 149, 167, 168, 173, 174, 175, 177, 178, 179, 181, 183, 186, 187, 188, 190, 191, 193, 194, 195, 196, 197, 198, 199, 200, 202, 205, 210, 212, 213, 219, 220, 223, 227, 229, 233, 239, 246, 247, 253, 255, 260, 261, 269, 288, 290, 293, 295, 297, 298, 301, 306, 309, 310, 313, 315, 317, 318, 319, 320, 321, 323, 325, 326, 328, 329, 330, 331, 336, 340, 341, 352, 353, 354, 355, 356, 358, 363, 366, 367, 369, 370, 371, 372, 374, 376, 377, 378, 379, 381, 382, 383, 384, 387, 391,
392, 393, 394, 395, 396, 398, 399, 400, 401, 402, 403, 404, 406, 408, 409, 416, 450, 451, 456, 458, 459, 460, 461, 466, 469, 470, 471, 472, 473, 475, 476, 479, 480, 484, 485, 493, 497, 505, 508, 509, 511, 512, 519, 522, 528, 530, 535, 540, 541, 543, 544, 545, 546, 548, 552, 554, 555, 568, 571, 572, 576, 588, 592, 594, 605, 607, 611, 615, 624, 625, 627, 628, 629, 630, 631, 632, 636, 637, 638, 640, 645, 647, 648, 651, 653, 654, 657, 663, 665, 670, 672, 674, 691 and 696.
In some embodiments, one aspect of the invention provides a compound selected from any one of Compounds Nos 100, 110, 111, 112, 113, 115, 118, 120, 121, 123, 126, 129, 130, 132, 139, 140, 141, 143, 146, 149, 154, 158, 160, 167, 168, 169, 172, 173, 174, 175, 176, 177, 178, 179, 181, 183, 184, 185, 186, 187, 188, 189, 190, 191, 193, 194, 195, 196, 197, 198, 199, 200, 201, 202, 203, 204, 205, 206, 208, 209, 210, 211, 212, 213, 214, 215, 216, 217, 218, 219, 220, 223, 224, 225, 226, 227, 228, 229, 232, 233, 239, 240, 241, 245, 246, 247, 248, 249, 250, 253, 254, 255, 257, 260, 261, 263, 266, 267, 268, 269, 270, 277, 281, 288, 289, 290, 293, 295, 296, 297, 298, 299, 301, 302, 306, 308, 309, 310, 313, 315, 317, 318, 319, 320, 321, 322, 323, 325, 326, 328, 329, 330, 331, 334, 335, 336, 340, 341, 344, 346, 351, 352, 353, 354, 355, 356, 358, 363, 366, 367, 369, 370, 371, 372, 374, 376, 377, 378, 379, 381, 382, 383, 384, 386, 387, 391, 392, 393, 394, 395, 396, 398, 399, 400, 401, 402, 403, 404, 406, 408, 409, and 416. In a more specific aspect of this embodiment, the invention provides a compound selected from any one of Compound Nos.100, 110, 111, 113, 120, 121, 126, 130, 132, 146, 149, 167, 168, 173, 174, 175, 177, 178, 179, 181, 183, 186, 187, 188, 190, 191, 193, 194, 195, 196, 197, 198, 199, 200, 202, 205, 210, 212, 213, 219, 220, 223, 227, 229, 233, 239, 247, 253, 255, 260, 261, 269, 288, 293, 295, 297, 298, 309, 313, 315, 317, 318, 320, 321, 325, 328, 329, 340, 341, 352, 369, 370, 371, 372, 374, 387, 394, 398, and 416.
Having thus described several aspects of several embodiments, it is to be appreciated various alterations, modifications, and improvements will readily occur to those skilled in the art. Such alterations, modifications, and improvements are intended to be part of this disclosure, and are intended to be within the spirit and scope of the invention. Accordingly, the foregoing description and drawings are by way of example only.

Claims

Claims
1. A compound having Formula I or a pharmaceutically acceptable salt or hydrate thereof:
Figure imgf000268_0001
wherein:
ring A is an optionally substituted 5-6 member monocyclic aryl or monocyclic heteroaryl;
ring B is an optionally substituted 5-6 member monocyclic aryl or monocyclic heteroaryl;
1 3
R and RJ are each independently selected from hydrogen, CrC4 alkyl, CrC4 haloalkyl, -0-CrC4 alkyl, and CN, wherein any alkyl portion of R1 is optionally substituted with -OH, NH2, NH(Ci-C4 alkyl), or N(C C4 alkyl)2;
R is selected from: -(C -C alkyl), -(C2-C6 alkenyl or alkynyl), -(C -C alkylene)-N(R6)-(Ci-C6 alkylene)-0-(Ci-C6 alkyl), -(Ci-C6 alkylene)-N(R6)-(C0-C6 alkylene)-Q, -(Ci-C6 alkylene)-N(R6)(R6), -(Ci-Ce alkylene)-N(R6)-S(0)1_2-(C1-C6 alkyl), -(Ci-Ce alkylene)-N(R6)-S(0)i_2-(Co-C6 alkyl)-Q, -(Ci-C6 alkylene)-S(0)i-2-N(R6)(R6), -(Ci-C4 alkylene)-S(0)i_2-N(R6)-(Ci-C6 alkylene)-Q, -C(0)N(R6)-(d-C6 alkylene)-C(O)- (Co-C6 alkylene)-0-(Ci-C6 alkyl), -C(0)N(R6)-(Ci-C6 alkylene)-C(O)-(C0-C6
alkylene)-O-(C0-C6 alkylene)-Q, -(Ci-Ce alkylene)-0-C(0)-(C1-C6 alkyl), -(Ci-Ce alkylene)-O-C(O)-(C0-C6 alkyl)-Q, -(Ci-C6 alkylene)-0-(C1-C6 alkyl), -(Ci-C6 alkylene)-0-(Ci-C6 alkylene)-Q, -(C0-C6 alkylene)-C(O)-(C0-C6 alkylene)-0-(Ci-C6 alkyl), -(Co-C6 alkylene)-C(O)-(C0-C6 alkylene)-0-(Ci-C6 alkylene)-Q, -(Ci-Ce alkylene)-0-C(0)-(C1-C6 alkyl), -(Ci-Ce alkylene)-O-C(O)-(C0-C6 alkylene)-Q, -(C0-C6 alkylene)-C(0)N(R6)-(C1-C6 alkyl), -(C0-C6 alkylene)-C(O)N(R6)-(C0-C6 alkylene)-Q, -(Ci-Ce alkylene)-N(R6)C(0)-(Ci-C6 alkyl), -(Ci-C6 alkylene)-N(R6)C(O)-(C0-C6 alkylene)-Q, -(C0-C6 alkylene)-S(O)0-2-(Ci-C6 alkyl), -(C0-C6 alkylene)-S(0)0-2-(Co-C6 alkylene)-Q, -(Ci-C6 alkylene)-N(R6)-C(0)-N(R6)-(C1-C6 alkyl), -(C0-C6 alkylene)-Q, -(Co-Ce alkylene)-C(0)-(C1-C6 alkyl), -(C0-C6 alkylene)-C(O)-(C0-C6 alkylene)-Q, wherein:
any alkyl or alkylene moiety present in R is optionally substituted with one or more -OH, -0(Ci-C4 alkyl) or halo;
any terminal methyl moiety present in R is optionally replaced with -CH2OH,
CF3, -CH2F, -CH2CI, C(0)CH3, C(0)CF3, CN, or C02H;
each R6 is independently selected from hydrogen and C]_-C alkyl; and
Q is selected from aryl, heteroaryl, carbocyclyl and heterocyclyl, any of which is optionally substituted; or
1 3
R and RJ are optionally taken together with the carbon atom to which they are attached to form C(=0), or
1 2
R and are optionally taken together to form substituted carbocyclyl, optionally substituted heterocyclyl or optionally substituted heteroaryl, wherein:
a. when ring A is unsubstituted phenyl, and ring B is phenyl substituted by methoxy or ethoxy; then said phenyl of ring B is not further substituted by oxazolyl;
b. when ring A is optionally substituted phenyl or optionally substituted pyridyl and ring B is optionally substituted phenyl; then the portion of the compound represented by -NH-C^XR2)^3) is not -NH(CH2)-aryl;
c. when ring A is optionally substituted phenyl, and ring B is optionally substituted phenyl or pyrrolyl; then the portion of the compound represented by
-NH-C^XR2)^3) is not -NH(CH2)C(0)NH2;
d. when ring A is phenyl substituted with 2 or more hydroxyl or methoxy, and ring B is optionally substituted phenyl; then the portion of the compound represented by -NH-C(R1)(R2)(R3) is not -NH-cycloheptyl;
e. when ring A is optionally substituted phenyl and ring B is optionally substituted
1 3
phenyl; then R and R do not form 2,2,6, 6,-tetramethylpiperidin-4-yl;
f. when ring A and ring B are optionally substituted phenyl; then the portion of the
1 2 3
compound represented by -NH-C(R )(R )(R ) is not cysteine, optionally substituted phenylalanine or leucine or methyl ester thereof; g. when ring A is phenyl or pyridin-3-yl optionally substituted with one or more substituents selected from halo, methyl or CF3, and ring B is phenyl optionally substituted with one or more substituents selected from halo, methyl, CF , methoxy, or CH=C(phenyl)CN; then the portion of the compound represented by -NHC^XR2)^3) is other than -NH(Ci-C8 alkylene)-N(Ra)(Ra), -NH-l-(aminomethyl)cyclopentylmethyl,
-NH-4-(aminomethyl)cyclohexylmethyl, wherein each Ra is hydrogen, CrC4 alkyl or two Ras are taken together with the nitrogen to which they are commonly bound to form morpholin-4-yl or pipieridin-l-yl;
h. when ring A is phenyl, 4-chlorophenyl or 4-methyl phenyl and ring B is 4-chlorophenyl or 3,4-dichlorophenyl; then the portion of the compound represented by -NHC(R1)(R2)(R3) is not -NH-isopropyl;
i. when ring A is unsubstituted phenyl and the portion of the compound represented by -NHC^XR2)^3) is -NH-CH2CH2N(CH3)2, -NH-CH2CH2-morpholin-4-yl or -NH-CH2CH2OH; then ring B is other than oxadiazole, imidazole, thiazole or oxazole each of which is substituted with -C(0)NHRb, wherein Rb is isopropyl, cyclopropyl or 2-chloro-6-methylphenyl;
j. when ring A is phenyl substituted with S02OH or S02Na and ring B is phenyl, or when ring B is phenyl substituted with S02OH and ring B is substituted phenyl; then the portion of the compound represented by -NHC(R 1 )(R2 )(R 3 ) is not -NH(CH2)2OH or -NH(CH2)CH(OH)CH3; and
k. the compound is other than:
(E)-3-(4-((4-((3-(diethylamino)propyl)amino)-6-phenyl-l,3,5-triazin-2-yl)amino)-2- methoxyphenyl)-2-phenylacrylonitrile ,
4-((4-((furan-2-ylmethyl)amino)-6-(pyridin-4-yl)-l,3,5-triazin-2-yl)amino)phenol, 3-(4-((5-aminopentyl)amino)-6-((3-fluorophenyl)amino)-l,3,5-triazin-2-yl)phenol,
N 2 ,6-bis(3-fluorophenyl)-N 4 -(piperidin-3-yl)-l,3,5-triazine-2,4-diamine,
N 2 -butyl-6-phenyl-N 4 -(p-tolyl)-l,3,5-triazine-2,4-diamine, N 2 -cyclohexyl-N 4 ,6-diphenyl- l,3,5-triazine-2,4-diamine, (R)-3-((4-(3-chlorophenyl)-6-(pyrrolidin-3-ylamino)-l,3,5-triazin-2-yl)amino)-4- methylbenzamide,
2-chloro-4-(methylsulfonyl)-N-[4-(phenylamino)-6-(2-pyridinyl)-l,3,5-triazin-2-yl]- benzamide,
N2^2-methoxyethyl)-A^-phenyl-6-[5-[6-(2,2,2-trifluoroethoxy)-3-pyridinyl]-l,2,4- oxadiazol-3-yl]-l,3,5-triazine-2,4-diamine,
2 -(2-furanylmethyl)-6-phenyl 4
N -N -[3-(trifluoromethyl)phenyl]-l,3,5-triazine-2,4- diamine,
6-(3-methoxyphenyl)-N2-methyl-A^-(3-nitrophenyl)-l,3,5-triazine-2,4-diamine, N2-butyl-N4-(4-methylphenyl)-6-phenyl- 1 ,3,5-triazine-2,4-diamine, and
4-[[4-(5-chloro-2-methylphenyl)-6-(methylamino)]-l,3,5-triazin-2-yl]amino- benzenemethanol .
2. The compound of claim 1, wherein R1 is independently selected from hydrogen, -C¾, -CH2CH3, -CH2OH, CN, or R1 and R3 are taken together to form =0.
3. The compound of claim 1, wherein R 1 and R 2 are taken together to form carbocyclyl or heterocyclyl, either of which is optionally substituted with up to 3 substituents independently selected from halo. CrC4 alkyl, CrC4 haloalkyl, CrC4 alkoxy, -CN, =0, -OH, and -C(0)d-C4 alkyl.
4. The compound of claim 1, wherein R is selected from: -(CrC4 alkyl) optionally
substituted with fluoro or -OH; -(C0-C4 alkylene)-0-(Ci-C4 alkyl), -(C0-C2
alkylene)-N(R6)-(C1-C6 alkyl), -(C0-C2 alkylene)-Q, and -O-(C0-C2 alkylene)-Q, wherein Q is optionally substituted with up to 3 substituents independently selected from C C4 alkyl, C C4 haloalkyl, Q-C4 alkoxy, =0, -C(0)-C C4 alkyl, -CN, and halo.
5. The compound of claim 4, wherein Q is selected from pyridinyl, tetrahydrofuranyl, cyclobutyl, cyclopropyl, phenyl, pyrazolyl, morpholinyl and oxetanyl, wherein Q is optionally substituted with up to 2 substituents independently selected from CrC4 alkyl, d-C4 haloalkyl, =0, fluoro, chloro, and bromo.
6. The compound of claim 1, wherein R 1 and R 2 are taken together to form cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, tetrahydrofuranyl, tetrahydropyranyl, oxetanyl, bicyclo[2.2.1]heptanyl, azetidinyl, phenyl and pyridinyl, any of which is optionally substituted with up to 2 substituents independently selected from d-C4 alkyl, d-C4 alkoxy, C3-C6 cycloalkyl, -OH, -C(0)CH3, fluoro, and chloro.
7. The compound of claim 1, wherein ring A is selected from phenyl, pyrazolyl, oxazolyl, isoxazolyl, pyridinyl, pyrimidinyl, pyrazinyl, and thiazolyl, wherein ring A is optionally substituted with up to two substituents independently selected from halo, -d-C4 alkyl, -C1-C4 haloalkyl, -C1-C4 hydroxyalkyl, -NH-S(0)2-(Ci-C4 alkyl), -S(0)2NH(Ci-C4 alkyl), -CN, -S(0)2-(Ci-C4 alkyl), C1-C4 alkoxy, -NH(d-C4 alkyl), -OH, -CN, and -NH2.
8. The compound of claim 1, wherein ring B is selected from phenyl, pyrazolyl, oxazolyl, isoxazolyl, thiazolyl, pyridinyl, pyrimidinyl, pyridazinyl, and pyrazinyl, wherein ring B is optionally substituted with up to two substituents independently selected from halo,
-C C4 alkyl, -C2-C4 alkynyl, -d-C4 haloalkyl, -d-C4 hydroxyalkyl, C3-C6 cycloalkyl, -(C0-C2 alkylene)-0-C1-C4 alkyl, -0-(Ci-C4 alkylene)-C3-C6 cycloalkyl,
-NH-S(0)2-(Ci-C4 alkyl), -S(0)2NH(d-C4 alkyl), -S(0)2-NH-(C3-C6 cycloalkyl), -S(0)2-(saturated heterocyclyl),-CN, -S(0)2-(d-C4 alkyl), -NH(Ci-C4 alkyl), -N(d-C4 alkyl)2, -OH, C(0)-0-(Ci-C4 alkyl), saturated heterocyclyl, and -NH2.
9. A compound having Structural Formula II:
Figure imgf000273_0001
H (II), or a pharmaceutically acceptable salt thereof, wherein:
Ring A' is selected from phenyl and pyridin-2-yl, wherein ring A' is optionally substituted with one or two substituents independently selected from chloro, fluoro, -CF3,
-CHF2, -CH3, -CH2CH3, -CF2CH3, -OH, -OCH3, -OCH2CH3, -NH2, -NH(CH3), and
-N(CH3)2;
Ring B' is selected from pyridin-3-yl, pyridin-4-yl, isoxazoly-4-yl, isoxazol-3-yl, thiazol-5-yl, pyrimidin-5-yl and pyrazol-4-yl, wherein ring B' is optionally substituted with one to two substituents independently selected from halo; -CN; -OH; C C4 alkyl optionally substituted with halo, CN or -OH; -S(0)2-Ci-C4 alkyl; -S(0)-Ci-C4 alkyl; -S(0)2-NH-Ci-C4 alkyl; -S(0)2-N(Ci-C4 alkyl)2; -S(0)2-azetidin-l-yl; -0-Ci-C4 alkyl; -CH2-0-CH3, morpholin-4-yl, cyclopropyl, -S(0)2-NH-cyclopropyl; -C(0)-0-CH3; and
-C(Rla)(R2a)(R3a) is selected from Ci-C6 alkyl optionally substituted with halo or -OH; -(Co-Ci alkylene)-cycloalkyl, wherein the alkylene is optionally substituted with methyl and the cycloalkyl is optionally substituted with halo, -OCH3 or methyl; saturated heterocyclyl optionally substituted with halo or methyl; -C(0)-0-Ci-C6 alkyl;
-C(0)-(Co-C1 alkylene)-cyclopropyl; and C(0)-benzyl.
10. The compound of claim 9, wherein ring A' is selected from 2-chlorophenyl, 2- fluorophenyl, 2-methoxyphenyl, 3-hydroxyphenyl, 6-aminopyridin-2-yl, 6-chloropyridin- 2-yl, 6-trifluoromethylpyridin-2-yl, and phenyl.
11. The compound of claim 9, wherein ring B' is selected from 2-(morpholin-4-yl)pyridin-4- yl, 2-dimethylaminopyridin-4-yl, 3-(2-methyoxyethyl)phenyl, 3,5-difluorophenyl, 3- chlorophenyl, 3-cyanomethylphenyl, 3-cyanophenyl, 3-cyclopropylaminosulfonylphenyl, 3-dimethylaminosulfonylphenyl, 3-ethylsulfonylphenyl, 3-fluorophenyl, 3- methylsulfonylphenyl, 4-fluorophenyl, 5-chloropyridin-3-yl, 5-cyanopyridin-3-yl, 5- cyanopyridin-3-yl, 5-cyanopyridin-4-yl, 5-fluoropyridin-3-yl, 5-trifluoromethypyridin-3- yl, 6-chloropyridin-4-yl, 6-cyanopyridin-4-yl, 6-cyclopropylpyridin-4-yl, 6- ethoxypyridin-4-yl, 6-fluoropyridin-3-yl, 6-fluoropyridin-4-yl, 6-methylpyridin-4-yl, 6- trifluoromethylpyridin-4-yl, isoxazol-4-yl, phenyl, pyridin-4-yl, and thiazol-5-yl.
12. The compound of claim 9, wherein the moiety represented by C(Rla)(R2a)(R3a) is selected from 2-hydroxycyclopentyl, 2-methylcyclopropyl, 3,3-difluorocyclobutyl, -(CH2)3CH3, -CH(CH3)-C(CH3)3, -CH(CH3)-CH2OCH3, -C(0)-C(CH3)3, -C(0)-CH(CH3)2,
-C(0)-cyclopropyl, -C(0)-OC(CH3)3, -C(0)-OCH2CH(CH3)2, -C(0)-OCH2CH3, -CH(CH3)-CH(CH3)2, -CH(CH3)-CH2CH3, -CH2C(CH3)2-CH2OH, CH2C(CH3)3, -CH2CF3, -CH2CH(CH3)2, -CH2CH(CH3)-CH2CH3, -CH2CH2CH(CH3)2, -CH2- cyclopropyl, cyclobutyl, cyclohexyl, cyclopentyl, cyclopropyl, isopropyl, oxetan-3-yl, bicyclo[2.2.1]heptanyl, tertrahydorpyran-4-yl, and tetrahydropyran-3-yl.
13. A pharmaceutical composition comprising a compound of claim 1, and a
pharmaceutically acceptable carrier.
14. The composition of claim 13, further comprising a second therapeutic agent useful in the treatment of cancer.
15. A method of treating a cancer characterized by the presence of an IDH2 mutation,
wherein the IDH2 mutation results in a new ability of the enzyme to catalyze the NAPH-dependent reduction of a-ketoglutarate to R(-)-2-hydroxyglutarate in a patient, comprising the step of administering to the patient in need thereof a composition of claim 10.
16. The method of claim 15, wherein the IDH2 mutation is an IDH2 R140Q or R172K mutation.
17. The method of claim 16, wherein the IDH2 mutation is an IDH2 R140Q mutation.
18. The method of claim 15, wherein the cancer is selected from glioblastoma (or glioma), myelodys plastic syndrome (MDS), myeloproliferative neoplasm (MPN), acute myelogenous leukemia (AML), sarcoma, melanoma, non-small cell lung cancer, chondrosarcoma, cholangiocarcinomas or angioimmunoblastic non-Hodgkin's lymphoma (NHL).
19. The method of claims 15, further comprising administering to the patient in need thereof a second therapeutic agent useful in the treatment of cancer.
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Cited By (71)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8883438B2 (en) 2009-10-21 2014-11-11 Agios Pharmaceuticals, Inc. Method for diagnosing cell proliferation disorders having a neoactive mutation at residue 97 of isocitrate dehydrogenase 1
WO2015006591A1 (en) * 2013-07-11 2015-01-15 Agios Pharmaceuticals, Inc. 2,4- or 4,6-diaminopyrimidine compounds as idh2 mutants inhibitors for the treatment of cancer
WO2015006592A1 (en) * 2013-07-11 2015-01-15 Agios Pharmaceuticals, Inc. N,6-bis(aryl or heteroaryl)-1,3,5-triazine-2,4-diamine compounds as idh2 mutants inhibitors for the treatment of cancer
WO2015003640A1 (en) * 2013-07-11 2015-01-15 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
WO2015003641A1 (en) * 2013-07-11 2015-01-15 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
WO2015018060A1 (en) * 2013-08-09 2015-02-12 Agios Pharmaceuticals, Inc. Crystalline forms of therapeutically active compounds and use thereof
WO2015144881A1 (en) * 2014-03-28 2015-10-01 Basf Se Diaminotriazine derivatives as herbicides
EP2930174A1 (en) * 2014-04-07 2015-10-14 Basf Se Diaminotriazine derivatives as herbicides
WO2015155129A1 (en) * 2014-04-07 2015-10-15 Basf Se Diaminotriazine compound
WO2016044787A1 (en) * 2014-09-19 2016-03-24 Forma Therapeutics, Inc. Pyridinyl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
WO2016044782A1 (en) * 2014-09-19 2016-03-24 Forma Therapeutics, Inc. Phenyl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
WO2016044789A1 (en) * 2014-09-19 2016-03-24 Forma Therapeutics, Inc. Pyridin-2(1h)-one quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
US20160089374A1 (en) * 2014-09-29 2016-03-31 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
CN105473560A (en) * 2013-07-11 2016-04-06 安吉奥斯医药品有限公司 Therapeutically active compounds and use methods thereof
WO2016126798A1 (en) 2015-02-04 2016-08-11 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
US9434979B2 (en) 2009-10-21 2016-09-06 Shin-San Michael Su Methods and compositions for cell-proliferation-related disorders
JP2016527279A (en) * 2013-08-02 2016-09-08 アギオス ファーマシューティカルス，インコーポレーテッド Therapeutically active compounds and methods of use
US9474779B2 (en) 2012-01-19 2016-10-25 Agios Pharmaceuticals, Inc. Therapeutically active compositions and their methods of use
WO2016171755A1 (en) 2015-04-21 2016-10-27 Forma Therapeutics, Inc. Fused-bicyclic aryl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
WO2016171756A1 (en) * 2015-04-21 2016-10-27 Forma Therapeutics, Inc. Quinolinone five-membered heterocyclic compounds as mutant-isocitrate dehydrogenase inhibitors
US9487495B2 (en) 2012-01-06 2016-11-08 The Scripts Research Institute Carbamate compounds and of making and using same
WO2016177347A1 (en) * 2015-05-07 2016-11-10 Teligene Ltd Heterocyclic compounds as idh2 inhibitors
US9512107B2 (en) 2012-01-06 2016-12-06 Agios Pharmaceuticals, Inc. Therapeutically active compositions and their methods of use
WO2017024134A1 (en) * 2015-08-05 2017-02-09 Agios Pharmaceuticals, Inc. Methods of preparing 6-(aryl or heteroaryl)-1,3,5-triazine-2,4-diols and 6-(aryl or heteroaryl)-1,3,5-triazine-2,4-diamines
US9579324B2 (en) 2013-07-11 2017-02-28 Agios Pharmaceuticals, Inc Therapeutically active compounds and their methods of use
WO2017069878A1 (en) * 2015-10-21 2017-04-27 NeuForm Pharmaceuticals, Inc. Deuterated compounds for treating hematologic malignancies, and compositions and methods thereof
US9662327B2 (en) 2011-06-17 2017-05-30 Agios Pharmaceuticals, Inc Phenyl and pyridinyl substituted piperidines and piperazines as inhibitors of IDH1 mutants and their use in treating cancer
WO2017096150A1 (en) * 2015-12-04 2017-06-08 Agios Pharmaceuticals, Inc. Methods of treatment of malignancies
WO2017140758A1 (en) 2016-02-19 2017-08-24 Debiopharm International S.A. Derivatives of 2-amino-4-(2-oxazolidinon-3-yl)-pyrimidine fused with a five-membered heteroaromatic ring in 5,6-position which are useful for the treatment of various cancers
US9771341B2 (en) 2015-03-18 2017-09-26 Abide Therapeutics, Inc. Piperazine carbamates and methods of making and using same
US9815817B2 (en) 2014-09-19 2017-11-14 Forma Therapeutics, Inc. Quinolinone pyrimidines compositions as mutant-isocitrate dehydrogenase inhibitors
US9856279B2 (en) 2011-06-17 2018-01-02 Agios Pharmaceuticals, Inc. Therapeutically active compositions and their methods of use
WO2018014852A1 (en) * 2016-07-21 2018-01-25 南京圣和药业股份有限公司 Chemical compound of isocitrate dehydrogenase inhibitor, and application thereof
WO2018048847A1 (en) 2016-09-07 2018-03-15 Celgene Corporation Tablet compositions
US9968595B2 (en) 2014-03-14 2018-05-15 Agios Pharmaceuticals, Inc. Pharmaceutical compositions of therapeutically active compounds
US9980961B2 (en) 2011-05-03 2018-05-29 Agios Pharmaceuticals, Inc. Pyruvate kinase activators for use in therapy
US9981930B1 (en) 2016-11-16 2018-05-29 Abide Therapeutics, Inc. MAGL inhibitors
US10029987B2 (en) 2009-06-29 2018-07-24 Agios Pharmaceuticals, Inc. Therapeutic compounds and compositions
US10093635B2 (en) 2016-11-16 2018-10-09 Abide Therapeutics, Inc. MAGL inhibitors
WO2018204787A1 (en) * 2017-05-05 2018-11-08 Memorial Sloan Kettering Cancer Center Methods of treatment of myeloproliferative neoplasm
US10202339B2 (en) 2012-10-15 2019-02-12 Agios Pharmaceuticals, Inc. Therapeutic compounds and compositions
CN110051673A (en) * 2018-01-19 2019-07-26 南京圣和药业股份有限公司 A kind of medical composition and its use comprising triazines IDH inhibitor
US10450302B2 (en) 2015-05-11 2019-10-22 Lundbeck La Jolla Research Center, Inc. Methods of treating inflammation or neuropathic pain
US10463753B2 (en) 2016-02-19 2019-11-05 Lundbeck La Jolla Research Center, Inc. Radiolabeled monoacylglycerol lipase occupancy probe
US10532047B2 (en) 2018-05-16 2020-01-14 Forma Therapeutics, Inc. Solid forms of ((S)-5-((1-(6-chloro-2-oxo-1,2-dihydroquinolin-3-yl)ethyl)amino)-1-methyl-6-oxo-1,6-dihydropyridine-2-carbonitrile
US10570106B2 (en) 2018-05-15 2020-02-25 Lundbeck La Jolla Research Center, Inc. MAGL inhibitors
US10610125B2 (en) 2009-03-13 2020-04-07 Agios Pharmaceuticals, Inc. Methods and compositions for cell-proliferation-related disorders
WO2020092894A1 (en) 2018-11-02 2020-05-07 Celgene Corporation Solid forms of 2-methyl-1-[(4-[6-(trifluoromethyl) pyridin-2-yl]-6-{[2-(trifluoromethyl)pyridin-4-yl]amino}-1,3,5-triazin-2-yl) amino]propan-2-ol
WO2020092915A1 (en) 2018-11-02 2020-05-07 Celgene Corporation Solid dispersions for treatment of cancer
WO2020092906A1 (en) 2018-11-02 2020-05-07 Celgene Corporation Co-crystals of 2-methyl-1 -[(4-[6-(trifluoromethyl)pyridin-2-yl]-6-{[2-(trifluoromethyl) pyridin-4-yl]amino}-1,3,5-triazin-2-yl)amino]propan-2-ol, compositions and methods of use thereof
US10653710B2 (en) 2015-10-15 2020-05-19 Agios Pharmaceuticals, Inc. Combination therapy for treating malignancies
US10689414B2 (en) 2013-07-25 2020-06-23 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
US10745383B2 (en) 2015-07-30 2020-08-18 Chia Tai Tianqing Pharmaceutical Group Co., Ltd. 1,3,5-triazine derivative and method of using same
WO2020239759A1 (en) 2019-05-27 2020-12-03 Sandoz Ag Amorphous enasidenib in a stabilized form
US10899737B2 (en) 2016-09-19 2021-01-26 Lundbeck La Jolla Research Center, Inc. Piperazine carbamates and methods of making and using same
WO2021057975A1 (en) * 2019-09-29 2021-04-01 贝达药业股份有限公司 Mutant idh2 inhibitor and application thereof
JP2021054856A (en) * 2014-02-20 2021-04-08 日本たばこ産業株式会社 Triazine compound and pharmaceutical use thereof
US10980788B2 (en) 2018-06-08 2021-04-20 Agios Pharmaceuticals, Inc. Therapy for treating malignancies
WO2021097160A1 (en) 2019-11-14 2021-05-20 Celgene Corporation Pediatric formulations for treatment of cancer
US11013734B2 (en) 2018-05-16 2021-05-25 Forma Therapeutics, Inc. Treating patients harboring an isocitrate dehydrogenase-1 (IDH-1) mutation
US11013733B2 (en) 2018-05-16 2021-05-25 Forma Therapeutics, Inc. Inhibiting mutant isocitrate dehydrogenase 1 (mlDH-1)
US11021464B2 (en) 2017-01-22 2021-06-01 Chia Tai Tianqing Pharmaceutical Group Co., Ltd. Crystalline forms of 4-(tert-butoxyamino)-6-(6-(trifluoromethyl)pyridin-2-yl)-N-(2-(trifluoromethyl)pyridin-4-yl)-1,3,5-triazin-2-amine methanesulfonic acid salt
EA038574B1 (en) * 2015-04-21 2021-09-16 Форма Терапьютикс, Инк. Pyridin-2(1h)-one quinolinone derivatives and pharmaceutical compositions thereof
US11234976B2 (en) 2015-06-11 2022-02-01 Agios Pharmaceuticals, Inc. Methods of using pyruvate kinase activators
US11311527B2 (en) 2018-05-16 2022-04-26 Forma Therapeutics, Inc. Inhibiting mutant isocitrate dehydrogenase 1 (mIDH-1)
US11376246B2 (en) 2018-05-16 2022-07-05 Forma Therapeutics, Inc. Inhibiting mutant IDH-1
US11414390B2 (en) 2017-09-07 2022-08-16 Hutchison Medipharma Limited Cycloolefin substituted heteroaromatic compounds and their use
US11419859B2 (en) 2015-10-15 2022-08-23 Servier Pharmaceuticals Llc Combination therapy for treating malignancies
RU2791798C1 (en) * 2022-12-29 2023-03-13 Федеральное государственное бюджетное учреждение "Российский научный центр радиологии и хирургических технологий имени академика А.М. Гранова" Министерства здравоохранения Российской Федерации Methyl 6-[(4-(aziridin-1-yl)-6-chloro-1,3,5-triazin-2-yl)amino]hexanoate, which has a cytotoxic effect
US11702393B2 (en) 2020-04-21 2023-07-18 H. Lundbeck A/S Synthesis of a monoacylglycerol lipase inhibitor
WO2023183520A1 (en) * 2022-03-24 2023-09-28 A2A Pharmaceuticals, Inc. Compositions and methods for treating cancer

Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR102316886B1 (en) * 2013-08-02 2021-10-19 아지오스 파마슈티컬스 아이엔씨. Therapeutically active compounds and their methods of use
JP6524119B2 (en) * 2014-03-14 2019-06-05 アジオス ファーマシューティカルズ， インコーポレイテッド Pharmaceutical compositions of therapeutically active compounds
US10905692B2 (en) 2015-10-15 2021-02-02 Agios Pharmaceuticals, Inc. Combination therapy for treating malignancies
NZ741433A (en) 2015-10-15 2024-07-26 Celgene Corp Combination therapy for treating malignancies
CN105399695B (en) * 2015-12-11 2019-04-19 浙江大学 Compound in triazine class and its preparation method and application
CN105384702B (en) * 2015-12-11 2018-04-10 浙江大学 Three substitution s-triazine compounds and preparation method thereof
CN105503754B (en) * 2015-12-11 2017-11-17 浙江大学 The triazine of 2 amino, 4 benzyl, 6 morpholine 1,3,5 and its preparation and application
ES2912909T3 (en) 2016-02-26 2022-05-30 Celgene Corp Enasidenib for use in the treatment of relapsed or refractory acute myeloid leukemia
CN105753801B (en) * 2016-03-25 2018-06-01 浙江工业大学 preparation method of s-triazine compound
CN105820133B (en) * 2016-03-25 2018-06-05 浙江工业大学 Polysubstituted s-triazine compound and preparation method and application thereof
EP3493809B1 (en) * 2016-08-03 2023-08-23 Celgene Corporation Enasidenib for treatment of myelodysplastic syndrome
SG11201913008TA (en) 2017-06-30 2020-01-30 Celgene Corp Compositions and methods of use of 2-(4-chlorophenyl)-n-((2-(2,6-doxopiperidin-3-yl)-1-oxoisoindolin-5-yl) methyl) -2,2-difluoroacetamide
CN109265444B (en) * 2017-07-17 2022-03-11 南京圣和药业股份有限公司 Optical isomer of substituted triazine IDH inhibitor and application thereof
CN110054617A (en) * 2018-01-19 2019-07-26 南京圣和药业股份有限公司 Compound in triazine class, preparation method and the usage
CN110054616B (en) * 2018-01-19 2021-11-23 南京圣和药业股份有限公司 Preparation method of triazine IDH inhibitor
CN110054615B (en) * 2018-01-19 2021-06-15 南京圣和药业股份有限公司 Crystal form of triazine IDH inhibitor mesylate
KR102328682B1 (en) * 2018-08-27 2021-11-18 주식회사 대웅제약 Novel heterocyclicamine derivatives and pharmaceutical composition comprising the same
CN111662271B (en) * 2019-03-08 2023-11-14 中国药科大学 Compound with IDH mutant inhibitory activity and preparation method and application thereof
CN111662275B (en) * 2019-03-08 2023-08-22 中国药科大学 Benzenesulfonamide IDH mutant inhibitor, preparation method and application thereof
CN111592524B (en) * 2020-05-20 2023-11-17 温州市天聚万迅信息科技有限公司 Preparation method of Enxidani
US20240092802A1 (en) * 2020-10-06 2024-03-21 Kures, Inc. Mu-opioid receptor agonists and uses therefor
KR20230145402A (en) * 2021-02-12 2023-10-17 르 라보레또레 쎄르비에르 Therapeutically active compounds and methods of their use
US11865079B2 (en) 2021-02-12 2024-01-09 Servier Pharmaceuticals Llc Therapeutically active compounds and their methods of use
CN113461660B (en) * 2021-06-11 2022-08-02 浙江大学 2,4, 6-trisubstituted-1, 3, 5-s-triazine compound, preparation and application thereof
CN118786119A (en) * 2022-03-15 2024-10-15 贝达药业股份有限公司 Mutant IDH1 and IDH2 inhibitors and application thereof
CN114773320A (en) * 2022-05-29 2022-07-22 重庆医科大学 1,3,5-triazine compound, preparation method and application thereof
CN115536637A (en) * 2022-10-24 2022-12-30 陕西中医药大学 S-triazine derivative and its synthesis method and use

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11158073A (en) * 1997-09-26 1999-06-15 Takeda Chem Ind Ltd Adenosine a3 antagonist
WO2008131547A1 (en) * 2007-04-30 2008-11-06 Prometic Biosciences Inc. 'triazine derivatives, compositions containing such derivatives, and methods of treatment of cancer and autoimmune diseases using such derivatives'
WO2010144338A1 (en) * 2009-06-08 2010-12-16 Abraxis Bioscience, Llc Triazine derivatives and their therapeutical applications

Family Cites Families (90)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2390529A (en) 1942-02-03 1945-12-11 Ernst A H Friedheim Hydrazino-1,3,5-triazino derivatives of substituted phenylarsenic compounds
BE754242A (en) 1970-07-15 1971-02-01 Geigy Ag J R DIAMINO-S-TRIAZINES AND DINITRO-S-TRIAZINES
US3867383A (en) 1971-03-29 1975-02-18 Ciba Geigy Corp Monoanthranilatoanilino-s-triazines
CH606334A5 (en) 1974-06-21 1978-10-31 Ciba Geigy Ag
JPS58186682A (en) 1982-04-27 1983-10-31 日本化薬株式会社 Dyeing of cellulose or cellulose containing fiber material
DE3512630A1 (en) 1985-04-06 1986-10-23 Hoechst Ag, 6230 Frankfurt METHOD FOR COLORING OR PRINTING CELLULOSE FIBERS OR CELLULOSE MIXED FIBERS
US5041443A (en) 1989-02-21 1991-08-20 Dainippon Pharmaceutical Co., Ltd. Medicament for treating cerebral insufficiency diseases, novel 2-(1-piperazinyl)-4-phenylcycloalkanopyrimidine derivatives, and process for the production thereof
DE69010232T2 (en) 1989-03-03 1994-12-01 Dainippon Pharmaceutical Co 2- (1-piperazinyl) -4-phenylcycloalkane pyridine derivatives, processes for their preparation and pharmaceutical compositions containing them.
ATE130882T1 (en) 1990-07-12 1995-12-15 Ciba Geigy Ag METHOD FOR THE PHOTOCHEMICAL AND THERMAL STABILIZATION OF POLYAMIDE FIBER MATERIALS.
JPH0499768A (en) 1990-08-17 1992-03-31 Dainippon Pharmaceut Co Ltd 4-(4-phenylpyridin-2-yl)piperazine-1-oxide derivative
CA2131004A1 (en) 1992-02-28 1993-09-02 Hideshi Kobayashi S-triazine derivative and remedy for estrogen-dependent disease containing said derivative as effective component
IL115420A0 (en) 1994-09-26 1995-12-31 Zeneca Ltd Aminoheterocyclic derivatives
FR2735127B1 (en) 1995-06-09 1997-08-22 Pf Medicament NEW HETEROAROMATIC PIPERAZINES USEFUL AS MEDICAMENTS.
GB9602166D0 (en) 1996-02-02 1996-04-03 Zeneca Ltd Aminoheterocyclic derivatives
JPH09291034A (en) 1996-02-27 1997-11-11 Yoshitomi Pharmaceut Ind Ltd Condensed pyridine compound and its use as medicine
WO1997044322A1 (en) 1996-05-20 1997-11-27 Darwin Discovery Limited Quinoline sulfonamides as tnf inhibitors and as pde-iv inhibitors
US5984882A (en) 1996-08-19 1999-11-16 Angiosonics Inc. Methods for prevention and treatment of cancer and other proliferative diseases with ultrasonic energy
EP0945446A4 (en) 1996-11-14 1999-12-08 Nissan Chemical Ind Ltd Cyanoethylmelamine derivatives and process for producing the same
US6399358B1 (en) 1997-03-31 2002-06-04 Thomas Jefferson University Human gene encoding human chondroitin 6-sulfotransferase
US7517880B2 (en) 1997-12-22 2009-04-14 Bayer Pharmaceuticals Corporation Inhibition of p38 kinase using symmetrical and unsymmetrical diphenyl ureas
UY25842A1 (en) 1998-12-16 2001-04-30 Smithkline Beecham Corp IL-8 RECEPTOR ANTAGONISTS
EP1187825A1 (en) 1999-06-07 2002-03-20 Shire Biochem Inc. Thiophene integrin inhibitors
ATE309207T1 (en) 1999-08-27 2005-11-15 Sugen Inc PHOSPHATE MIMETICS AND TREATMENT METHODS USING PHOSPHATASE INHIBITORS
AU2001267910A1 (en) 2000-07-03 2002-01-14 Kansai Paint Co. Ltd. Gas-barrier film
KR20030024799A (en) 2000-07-20 2003-03-26 뉴로젠 코포레이션 Capsaicin receptor ligands
HUP0402352A2 (en) 2001-06-19 2005-02-28 Bristol-Myers Squibb Co. Pyrimidine derivatives for use as phosphodiesterase (pde)7 inhibitors and pharmaceutical compositions containing them
JP4344241B2 (en) 2001-08-17 2009-10-14 チバ ホールディング インコーポレーテッド Triazine derivatives and their use as sunscreens
JP4753336B2 (en) 2001-09-04 2011-08-24 日本化薬株式会社 Novel allyl compound and process for producing the same
WO2003037346A1 (en) * 2001-10-31 2003-05-08 Cell Therapeutics, Inc. 6-phenyl-n-phenyl-(1,3,5) -triazine-2,4-diamine derivatives and related compounds with lysophphosphatidic acid acyltransferase beta (lpaat-beta) inhibitory activity for use in the treatment of cancer
US6878196B2 (en) 2002-01-15 2005-04-12 Fuji Photo Film Co., Ltd. Ink, ink jet recording method and azo compound
US20040067234A1 (en) 2002-07-11 2004-04-08 Paz Einat Isocitrate dehydrogenase and uses thereof
SI2256108T1 (en) 2002-07-18 2016-05-31 Janssen Pharmaceutica N.V. Substituted triazine kinase inhibitors
JP2004107220A (en) 2002-09-13 2004-04-08 Mitsubishi Pharma Corp TNF-alpha PRODUCTION INHIBITOR
CL2003002353A1 (en) 2002-11-15 2005-02-04 Vertex Pharma COMPOUNDS DERIVED FROM DIAMINOTRIAZOLS, INHIBITORS D ELA PROTEINA QUINASA; PHARMACEUTICAL COMPOSITION; PREPARATION PROCEDURE; AND ITS USE OF THE COMPOUND IN THE TREATMENT OF DISEASES OF ALLERGIC DISORDERS, PROLIFERATION, AUTOIMMUNES, CONDIC
EP1575580A4 (en) 2002-12-02 2009-06-10 Arqule Inc Method of treating cancers
ES2373947T3 (en) 2002-12-16 2012-02-10 Genmab A/S HUMAN MONOCLONAL ANTIBODIES AGAINST INTERLEUCINE 8 (IL-8).
CA2513399A1 (en) 2003-01-10 2004-07-29 Threshold Pharmaceuticals, Inc. Treatment of cancer with 2-deoxyglucose
US7358262B2 (en) 2003-01-29 2008-04-15 Whitehead Institute For Biomedical Research Identification of genotype-selective anti-tumor agents
WO2004073619A2 (en) 2003-02-14 2004-09-02 Smithkline Beecham Corporation Ccr8 antagonists
WO2004074438A2 (en) 2003-02-14 2004-09-02 Smithkline Beecham Corporation Ccr8 antagonists
EP1689722A2 (en) 2003-10-10 2006-08-16 Bayer Pharmaceuticals Corporation 4-aminopyrimidine derivatives for treatment of hyperproliferative disorders
AU2003297904A1 (en) 2003-12-12 2005-07-14 University Of Maryland, Baltimore Immunomodulatory compounds that target and inhibit the py+3 binding site of tyrosene kinase p56 lck sh2 domain
EP1708712A1 (en) 2003-12-24 2006-10-11 Scios, Inc. Treatment of malignant gliomas with tgf-beta inhibitors
US7622486B2 (en) 2004-09-23 2009-11-24 Reddy Us Therapeutics, Inc. Pyridine compounds, process for their preparation and compositions containing them
WO2006070198A1 (en) 2004-12-30 2006-07-06 Astex Therapeutics Limited Pyrazole derivatives as that modulate the activity of cdk, gsk and aurora kinases
BRPI0606930A2 (en) 2005-01-25 2009-12-01 Astrazeneca Ab compound or a pharmaceutically acceptable salt thereof, process for preparing a compound or a pharmaceutically acceptable salt thereof, pharmaceutical composition, use of a compound or a pharmaceutically acceptable salt thereof, and methods for producing a drug inhibiting effect. b-raf in a warm-blooded animal, for producing an anti-cancer effect on a warm-blooded animal and for treating diseases of an animal in a warm-blooded animal
AU2006254834B2 (en) 2005-06-08 2012-09-20 Millennium Pharmaceuticals, Inc. Treatment of patients with cancer therapy
KR20080049767A (en) 2005-08-26 2008-06-04 라보라뚜와르 세로노 에스. 에이. Pyrazine derivatives and use as pi3k inhibitors
US8133900B2 (en) 2005-11-01 2012-03-13 Targegen, Inc. Use of bi-aryl meta-pyrimidine inhibitors of kinases
TW200815426A (en) 2006-06-28 2008-04-01 Astrazeneca Ab New pyridine analogues II 333
WO2008070661A1 (en) 2006-12-04 2008-06-12 Neurocrine Biosciences, Inc. Substituted pyrimidines as adenosine receptor antagonists
WO2008076883A2 (en) 2006-12-15 2008-06-26 Abraxis Bioscience, Inc. Triazine derivatives and their therapeutical applications
AU2008262291A1 (en) 2007-06-11 2008-12-18 Miikana Therapeutics, Inc. Substituted pyrazole compounds
BRPI0814628B1 (en) 2007-07-20 2022-04-05 Nerviano Medical Sciences S.R.L. Active substituted indazole derivatives as kinase inhibitors
WO2009027736A2 (en) * 2007-08-27 2009-03-05 Astrazeneca Ab 2,4 diaminopyrimid'lnes for the treatment of myeloproliferative disorders and cancer
CN101981010A (en) 2007-10-10 2011-02-23 武田药品工业株式会社 Amide compound
JP2011507910A (en) 2007-12-21 2011-03-10 ユニバーシティー オブ ロチェスター Methods for changing the lifetime of eukaryotes
GB0805477D0 (en) 2008-03-26 2008-04-30 Univ Nottingham Pyrimidines triazines and their use as pharmaceutical agents
JP5277685B2 (en) 2008-03-26 2013-08-28 富士ゼロックス株式会社 Electrophotographic photosensitive member, image forming apparatus, process cartridge, and image forming method
CN101575408B (en) 2008-05-09 2013-10-30 Mca技术有限公司 Polytriazinyl compounds as flame retardants and light stabilizers
FR2932483A1 (en) 2008-06-13 2009-12-18 Cytomics Systems COMPOUNDS USEFUL FOR THE TREATMENT OF CANCERS.
WO2010007756A1 (en) 2008-07-14 2010-01-21 塩野義製薬株式会社 Pyridine derivative having ttk inhibition activity
WO2010028179A1 (en) 2008-09-03 2010-03-11 Dr. Reddy's Laboratories Ltd. Heterocyclic compounds as gata modulators
PL2546365T3 (en) 2008-09-03 2017-07-31 The Johns Hopkins University Genetic alterations in isocitrate dehydrogenase and other genes in malignant glioma
JP2010079130A (en) 2008-09-29 2010-04-08 Fuji Xerox Co Ltd Electrophotographic photoreceptor, process cartridge, and image forming apparatus
JP2010181540A (en) 2009-02-04 2010-08-19 Fuji Xerox Co Ltd Electrophotographic photoreceptor, process cartridge and image forming apparatus
ES2453474T3 (en) 2009-02-06 2014-04-07 Nippon Shinyaku Co., Ltd. Aminopyrazine derivatives and corresponding medicine
WO2010105243A1 (en) 2009-03-13 2010-09-16 Agios Pharmaceuticals, Inc. Methods and compositions for cell-proliferation-related disorders
US8261872B2 (en) * 2009-06-08 2012-09-11 Clark Equipment Company Work machine having modular ignition switch keypad with latching output
CA2765050A1 (en) 2009-06-09 2010-12-16 California Capital Equity, Llc Ureidophenyl substituted triazine derivatives and their therapeutical applications
JP2012529518A (en) 2009-06-09 2012-11-22 アブラクシス バイオサイエンス リミテッド ライアビリティー カンパニー Pyridyl-triazine inhibitors of hedgehog signaling
WO2011005209A1 (en) 2009-07-10 2011-01-13 Milux Holding S.A. Knee joint device and method
JP5473851B2 (en) 2009-09-30 2014-04-16 富士フイルム株式会社 Polymer film, retardation film, polarizing plate and liquid crystal display device
CA2793836C (en) 2009-10-21 2020-03-24 Agios Pharmaceuticals, Inc. Methods and compositions for cell-proliferation-related disorders
EP3561077B1 (en) 2009-10-21 2022-12-21 Les Laboratoires Servier Methods for cell-proliferation-related disorders
JP5967827B2 (en) 2009-12-09 2016-08-10 アジオス ファーマシューティカルズ， インコーポレイテッド Therapeutically active compounds for the treatment of cancer characterized by having an IDH variant
EP2553116A4 (en) 2010-04-01 2013-10-23 Agios Pharmaceuticals Inc Methods of identifying a candidate compound
JP6081354B2 (en) 2010-07-16 2017-02-15 アジオス ファーマシューティカルズ， インコーポレイテッド Therapeutically active compositions and methods of their use
CN103347866B (en) 2010-11-29 2016-05-18 加林制药公司 As the noval chemical compound of the respiratory stimulant for the treatment of control of breathing discomfort or disease
TW201636330A (en) 2011-05-24 2016-10-16 拜耳知識產權公司 4-aryl-N-phenyl-1,3,5-triazin-2-amines containing a sulfoximine group
CN102827170A (en) 2011-06-17 2012-12-19 安吉奥斯医药品有限公司 Active treatment compositions and use method thereof
CN102827073A (en) 2011-06-17 2012-12-19 安吉奥斯医药品有限公司 Therapeutically active compositions and application methods thereof
CN102659765B (en) 2011-12-31 2014-09-10 沈阳药科大学 Pyrimidine and triazine compound preparation method and application
CN107982266B (en) 2012-01-06 2021-07-30 H.隆德贝克有限公司 Carbamate compounds and methods of making and using the same
SI2800743T1 (en) * 2012-01-06 2018-08-31 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
US9474779B2 (en) 2012-01-19 2016-10-25 Agios Pharmaceuticals, Inc. Therapeutically active compositions and their methods of use
MX350432B (en) 2012-01-19 2017-09-06 Agios Pharmaceuticals Inc Therapeutically active compounds and their methods of use.
US20150011751A1 (en) 2012-03-09 2015-01-08 Carna Biosciences, Inc. Novel triazine derivative
US9579324B2 (en) 2013-07-11 2017-02-28 Agios Pharmaceuticals, Inc Therapeutically active compounds and their methods of use
US20150031627A1 (en) 2013-07-25 2015-01-29 Agios Pharmaceuticals, Inc Therapeutically active compounds and their methods of use

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11158073A (en) * 1997-09-26 1999-06-15 Takeda Chem Ind Ltd Adenosine a3 antagonist
WO2008131547A1 (en) * 2007-04-30 2008-11-06 Prometic Biosciences Inc. 'triazine derivatives, compositions containing such derivatives, and methods of treatment of cancer and autoimmune diseases using such derivatives'
WO2010144338A1 (en) * 2009-06-08 2010-12-16 Abraxis Bioscience, Llc Triazine derivatives and their therapeutical applications

Non-Patent Citations (11)

* Cited by examiner, † Cited by third party
Title
AGHILI, M.; ZAHEDI, F.; RAFIEE, J, NEUROONCOL, vol. 91, 2009, pages 233 - 6
BERGE ET AL.: "Pharmaceutically Acceptable Salts", J. PHARM. SCI., vol. 66, 1977, pages 1 - 19
CUI-JUAN WANG ET AL.: "A novel ligand N,N'-di(2-pyridyl)-2,4-diamino-6-phenyl-1,3,5-triazine (dpdapt) and its complexes: [Cu(dpdapt)Clz] and [Cu(dpdapt)(N03)(H20)]-NO3 ·HZO", POLYHEDRON, vol. 25, 2006, pages 195 - 202, XP024915671 *
KOLKER, S. ET AL., EUR J NEUROSCI, vol. 16, 2002, pages 21 - 8
KOLKER, S.; MAYATEPEK, E.; HOFFMANN, G. F., NEUROPEDIATRICS, vol. 33, 2002, pages 225 - 31
LATINI, A. ET AL., EUR J NEUROSCI, vol. 17, 2003, pages 2017 - 22
LUO ET AL., J CHROMATOGR A, vol. 1147, 2007, pages 153 - 64
MUNGER ET AL., NAT BIOTECHNOL, vol. 26, 2008, pages 1179 - 86
See also references of EP2800743A4
STRUYS, E. A. ET AL., AM J HUM GENET, vol. 76, 2005, pages 358 - 60
WAJNER, M.; LATINI, A.; WYSE, A. T.; DUTRA-FILHO, C. S., J INHERIT METAB DIS, vol. 27, 2004, pages 427 - 48

Cited By (191)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10610125B2 (en) 2009-03-13 2020-04-07 Agios Pharmaceuticals, Inc. Methods and compositions for cell-proliferation-related disorders
USRE49582E1 (en) 2009-06-29 2023-07-18 Agios Pharmaceuticals, Inc. Therapeutic compounds and compositions
US10029987B2 (en) 2009-06-29 2018-07-24 Agios Pharmaceuticals, Inc. Therapeutic compounds and compositions
US10988448B2 (en) 2009-06-29 2021-04-27 Agios Pharmaceuticals, Inc. Therapeutic compounds and compositions
US11866411B2 (en) 2009-06-29 2024-01-09 Agios Pharmaceutical, Inc. Therapeutic compounds and compositions
US9982309B2 (en) 2009-10-21 2018-05-29 Agios Pharmaceuticals, Inc. Method for treating cell proliferation related disorders
US8883438B2 (en) 2009-10-21 2014-11-11 Agios Pharmaceuticals, Inc. Method for diagnosing cell proliferation disorders having a neoactive mutation at residue 97 of isocitrate dehydrogenase 1
US9434979B2 (en) 2009-10-21 2016-09-06 Shin-San Michael Su Methods and compositions for cell-proliferation-related disorders
US10711314B2 (en) 2009-10-21 2020-07-14 Agios Pharmaceuticals, Inc. Methods for diagnosing IDH-mutant cell proliferation disorders
US9980961B2 (en) 2011-05-03 2018-05-29 Agios Pharmaceuticals, Inc. Pyruvate kinase activators for use in therapy
US11793806B2 (en) 2011-05-03 2023-10-24 Agios Pharmaceuticals, Inc. Pyruvate kinase activators for use in therapy
US10632114B2 (en) 2011-05-03 2020-04-28 Agios Pharmaceuticals, Inc. Pyruvate kinase activators for use in therapy
US9856279B2 (en) 2011-06-17 2018-01-02 Agios Pharmaceuticals, Inc. Therapeutically active compositions and their methods of use
US9662327B2 (en) 2011-06-17 2017-05-30 Agios Pharmaceuticals, Inc Phenyl and pyridinyl substituted piperidines and piperazines as inhibitors of IDH1 mutants and their use in treating cancer
US12018004B2 (en) 2012-01-06 2024-06-25 H. Lundbeck A/S Carbamate compounds and methods of making and using same
US11021453B2 (en) 2012-01-06 2021-06-01 Lundbeck La Jolla Research Center, Inc. Carbamate compounds and methods of making and using same
US9957242B2 (en) 2012-01-06 2018-05-01 The Scripps Research Institute Carbamate compounds and methods of making and using same
US11530189B2 (en) 2012-01-06 2022-12-20 H. Lundbecka/S Carbamate compounds and methods of making and using same
US11505538B1 (en) 2012-01-06 2022-11-22 Servier Pharmaceuticals Llc Therapeutically active compounds and their methods of use
US10294215B2 (en) 2012-01-06 2019-05-21 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
US9512107B2 (en) 2012-01-06 2016-12-06 Agios Pharmaceuticals, Inc. Therapeutically active compositions and their methods of use
US9656999B2 (en) 2012-01-06 2017-05-23 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
US9732062B2 (en) 2012-01-06 2017-08-15 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
US9487495B2 (en) 2012-01-06 2016-11-08 The Scripts Research Institute Carbamate compounds and of making and using same
US11667673B2 (en) 2012-01-19 2023-06-06 Servier Pharmaceuticals Llc Therapeutically active compounds and their methods of use
US10717764B2 (en) 2012-01-19 2020-07-21 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
US9474779B2 (en) 2012-01-19 2016-10-25 Agios Pharmaceuticals, Inc. Therapeutically active compositions and their methods of use
US10640534B2 (en) 2012-01-19 2020-05-05 Agios Pharmaceuticals, Inc. Therapeutically active compositions and their methods of use
US9850277B2 (en) 2012-01-19 2017-12-26 Agios Pharmaceuticals, Inc. Therapeutically active compositions and their methods of use
US10202339B2 (en) 2012-10-15 2019-02-12 Agios Pharmaceuticals, Inc. Therapeutic compounds and compositions
CN105492435A (en) * 2013-07-11 2016-04-13 安吉奥斯医药品有限公司 N,6-bis(aryl or heteroaryl)-1,3,5-triazine-2,4-diamine compounds as IDH2 mutants inhibitors for the treatment of cancer
US10172864B2 (en) 2013-07-11 2019-01-08 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
US9579324B2 (en) 2013-07-11 2017-02-28 Agios Pharmaceuticals, Inc Therapeutically active compounds and their methods of use
US10946023B2 (en) 2013-07-11 2021-03-16 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
AU2014287122B2 (en) * 2013-07-11 2018-10-25 Les Laboratoires Servier N,6-bis(aryl or heteroaryl)-1,3,5-triazine-2,4-diamine compounds as IDH2 mutants inhibitors for the treatment of cancer
EA030199B1 (en) * 2013-07-11 2018-07-31 Аджиос Фармасьютикалз, Инк. Therapeutically active compounds and methods of use thereof
WO2015006591A1 (en) * 2013-07-11 2015-01-15 Agios Pharmaceuticals, Inc. 2,4- or 4,6-diaminopyrimidine compounds as idh2 mutants inhibitors for the treatment of cancer
US9724350B2 (en) 2013-07-11 2017-08-08 Agios Pharmaceuticals, Inc. N,6-bis(aryl or heteroaryl)-1,3,5-triazine-2,4-diamine compounds as IDH2 mutants inhibitors for the treatment of cancer
EA030199B9 (en) * 2013-07-11 2021-08-26 Аджиос Фармасьютикалз, Инк. Therapeutically active compounds and methods of use thereof
US10028961B2 (en) 2013-07-11 2018-07-24 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
US10111878B2 (en) 2013-07-11 2018-10-30 Agios Pharmaceuticals, Inc. N,6-bis(aryl or heteroaryl)-1,3,5-triazine-2,4-diamine compounds as IDH2 mutants inhibitors for the treatment of cancer
US10017495B2 (en) 2013-07-11 2018-07-10 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
CN105492435B (en) * 2013-07-11 2018-06-29 安吉奥斯医药品有限公司 Compound as IDH2 mutant inhibitor
AU2014287122B9 (en) * 2013-07-11 2018-11-01 Les Laboratoires Servier N,6-bis(aryl or heteroaryl)-1,3,5-triazine-2,4-diamine compounds as IDH2 mutants inhibitors for the treatment of cancer
AU2014287121B2 (en) * 2013-07-11 2018-11-15 Agios Pharmaceuticals, Inc. 2,4- or 4,6-diaminopyrimidine compounds as IDH2 mutants inhibitors for the treatment of cancer
WO2015006592A1 (en) * 2013-07-11 2015-01-15 Agios Pharmaceuticals, Inc. N,6-bis(aryl or heteroaryl)-1,3,5-triazine-2,4-diamine compounds as idh2 mutants inhibitors for the treatment of cancer
CN105473560B (en) * 2013-07-11 2020-01-17 安吉奥斯医药品有限公司 Therapeutically active compounds and methods of use thereof
AU2019201179B2 (en) * 2013-07-11 2021-03-25 Les Laboratoires Servier Therapeutically active compounds and their methods of use
WO2015003640A1 (en) * 2013-07-11 2015-01-15 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
US10376510B2 (en) 2013-07-11 2019-08-13 Agios Pharmaceuticals, Inc. 2,4- or 4,6-diaminopyrimidine compounds as IDH2 mutants inhibitors for the treatment of cancer
CN105473560A (en) * 2013-07-11 2016-04-06 安吉奥斯医药品有限公司 Therapeutically active compounds and use methods thereof
US11844758B2 (en) 2013-07-11 2023-12-19 Servier Pharmaceuticals Llc Therapeutically active compounds and their methods of use
WO2015003641A1 (en) * 2013-07-11 2015-01-15 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
WO2015003355A3 (en) * 2013-07-11 2015-03-12 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
EA032070B1 (en) * 2013-07-11 2019-04-30 Аджиос Фармасьютикалз, Инк. N,6-bis(aryl or heteroaryl)-1,3,5-triazine-2,4-diamine compounds as idh2 mutants inhibitors for the treatment of cancer
US10689414B2 (en) 2013-07-25 2020-06-23 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
US11021515B2 (en) 2013-07-25 2021-06-01 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
EP3932408A1 (en) 2013-08-02 2022-01-05 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
EP3566706A1 (en) 2013-08-02 2019-11-13 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
AU2018247242B2 (en) * 2013-08-02 2020-03-12 Les Laboratoires Servier Therapeutically active compounds and their methods of use
US10093654B2 (en) 2013-08-02 2018-10-09 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
JP2016527279A (en) * 2013-08-02 2016-09-08 アギオス ファーマシューティカルス，インコーポレーテッド Therapeutically active compounds and methods of use
JP2019142930A (en) * 2013-08-02 2019-08-29 アギオス ファーマシューティカルス，インコーポレーテッド Therapeutically active compounds and their methods of use
JP2021176893A (en) * 2013-08-02 2021-11-11 アギオス ファーマシューティカルス，インコーポレーテッド Therapeutically active compound and its method of use
AU2014295938B2 (en) * 2013-08-02 2018-07-19 Les Laboratoires Servier Therapeutically active compounds and their methods of use
US9738625B2 (en) 2013-08-02 2017-08-22 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
TWI666208B (en) * 2013-08-02 2019-07-21 美商阿吉斯藥品有限公司 Therapeutically active compounds and their methods of use
US10730854B2 (en) 2013-08-02 2020-08-04 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
TWI701242B (en) * 2013-08-02 2020-08-11 美商阿吉斯藥品股份有限公司 Therapeutically active compounds and their methods of use
WO2015018060A1 (en) * 2013-08-09 2015-02-12 Agios Pharmaceuticals, Inc. Crystalline forms of therapeutically active compounds and use thereof
JP2021054856A (en) * 2014-02-20 2021-04-08 日本たばこ産業株式会社 Triazine compound and pharmaceutical use thereof
US9968595B2 (en) 2014-03-14 2018-05-15 Agios Pharmaceuticals, Inc. Pharmaceutical compositions of therapeutically active compounds
US10799490B2 (en) 2014-03-14 2020-10-13 Agios Pharmaceuticals, Inc. Pharmaceutical compositions of therapeutically active compounds
US10449184B2 (en) 2014-03-14 2019-10-22 Agios Pharmaceuticals, Inc. Pharmaceutical compositions of therapeutically active compounds
US11504361B2 (en) 2014-03-14 2022-11-22 Servier Pharmaceuticals Llc Pharmaceutical compositions of therapeutically active compounds
WO2015144881A1 (en) * 2014-03-28 2015-10-01 Basf Se Diaminotriazine derivatives as herbicides
CN106132946A (en) * 2014-03-28 2016-11-16 巴斯夫欧洲公司 Diaminourea pyrrolotriazine derivatives as herbicide
EP2930174A1 (en) * 2014-04-07 2015-10-14 Basf Se Diaminotriazine derivatives as herbicides
WO2015155129A1 (en) * 2014-04-07 2015-10-15 Basf Se Diaminotriazine compound
AU2019283765B2 (en) * 2014-09-19 2021-05-13 Forma Therapeutics, Inc. Pyridin-2(1h)-one quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
US10414752B2 (en) 2014-09-19 2019-09-17 Forma Therapeutics, Inc. Pyridin-2(1H)-one quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
WO2016044782A1 (en) * 2014-09-19 2016-03-24 Forma Therapeutics, Inc. Phenyl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
AU2021215141B2 (en) * 2014-09-19 2023-10-19 Forma Therapeutics, Inc. Pyridin-2(1h)-one quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
EP3447050A1 (en) 2014-09-19 2019-02-27 Forma Therapeutics, Inc. Pyridin-2(1h)-one quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
US10253015B2 (en) 2014-09-19 2019-04-09 Forma Tm2, Inc. Pyridinyl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
US10266495B2 (en) 2014-09-19 2019-04-23 Forma Tm2, Inc. Phenyl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
WO2016044789A1 (en) * 2014-09-19 2016-03-24 Forma Therapeutics, Inc. Pyridin-2(1h)-one quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
US10280150B2 (en) 2014-09-19 2019-05-07 Forma Tm2, Inc. Quinolinone pyrimidines compositions as mutant-isocitrate dehydrogenase inhibitors
WO2016044787A1 (en) * 2014-09-19 2016-03-24 Forma Therapeutics, Inc. Pyridinyl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
US11498913B2 (en) 2014-09-19 2022-11-15 Forma Therapeutics, Inc. Pyridin-2(1H)-one quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
CN111909130B (en) * 2014-09-19 2023-10-31 福马治疗股份有限公司 Pyridin-2 (1H) -one quinolinone derivatives as mutant isocitrate dehydrogenase inhibitors
JP2017528491A (en) * 2014-09-19 2017-09-28 フォーマ セラピューティクス，インコーポレイテッド Pyridinylquinolinone derivatives as mutant isocitrate dehydrogenase inhibitors
KR20170063742A (en) * 2014-09-19 2017-06-08 포르마 세라퓨틱스 인크. Pyridin-2(1h)-one quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
US9834539B2 (en) 2014-09-19 2017-12-05 Forma Therapeutics, Inc. Pyridin-2(1H)-one quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
US9815817B2 (en) 2014-09-19 2017-11-14 Forma Therapeutics, Inc. Quinolinone pyrimidines compositions as mutant-isocitrate dehydrogenase inhibitors
KR102209667B1 (en) 2014-09-19 2021-01-29 포르마 세라퓨틱스 인크. Pyridin-2(1h)-one quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
EP4257131A2 (en) 2014-09-19 2023-10-11 Forma Therapeutics, Inc. Pyridin-2(1h)-one quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
US10889567B2 (en) 2014-09-19 2021-01-12 Forma Therapeutics, Inc. Pyridin-2(1H)-one quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
CN111909130A (en) * 2014-09-19 2020-11-10 福马治疗股份有限公司 Pyridin-2 (1H) -one quinolinone derivatives as mutant isocitrate dehydrogenase inhibitors
US10005734B2 (en) 2014-09-19 2018-06-26 Forma Therapeutics, Inc. Pyridin-2(1H)-one quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
AU2015317329B2 (en) * 2014-09-19 2019-10-31 Forma Therapeutics, Inc. Pyridin-2(1H)-one quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
EP3733662A1 (en) 2014-09-19 2020-11-04 Forma Therapeutics, Inc. Pyridin-2(1h)-one quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
EP4257131A3 (en) * 2014-09-19 2024-01-10 Forma Therapeutics, Inc. Pyridin-2(1h)-one quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
CN107001328A (en) * 2014-09-19 2017-08-01 福马治疗股份有限公司 It is used as pyridine 2 (1H) ketone qualone derivative of saltant type isocitric dehydrogenase inhibitor
JP2017528487A (en) * 2014-09-19 2017-09-28 フォーマ セラピューティクス，インコーポレイテッド Pyridine-2 (1H) -onquinolinone derivatives as mutant isocitrate dehydrogenase inhibitors
EA034336B1 (en) * 2014-09-19 2020-01-29 Форма Терапьютикс, Инк. Pyridin-2(1h)-one quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
US10550099B2 (en) 2014-09-19 2020-02-04 Forma Therapeutics, Inc. Quinolinone pyrimidines compositions as mutant-isocitrate dehydrogenase inhibitors
US10550098B2 (en) 2014-09-19 2020-02-04 Forma Therapeutics, Inc. Pyridin-2(1H)-one quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
US9771349B2 (en) 2014-09-19 2017-09-26 Forma Therapeutics, Inc. Pyridinyl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
AU2015317327B9 (en) * 2014-09-19 2020-04-09 Forma Therapeutics, Inc. Pyridinyl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
JP2017528489A (en) * 2014-09-19 2017-09-28 フォーマ セラピューティクス，インコーポレイテッド Phenylquinolinone derivatives as mutant isocitrate dehydrogenase inhibitors
AU2015317327B2 (en) * 2014-09-19 2020-03-19 Forma Therapeutics, Inc. Pyridinyl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
JP2017529382A (en) * 2014-09-29 2017-10-05 アギオス ファーマシューティカルス，インコーポレーテッド Compounds having therapeutic activity and methods of use thereof
JP2020147571A (en) * 2014-09-29 2020-09-17 アギオス ファーマシューティカルス，インコーポレーテッド Therapeutically active compounds and their methods of use
US10105369B2 (en) 2014-09-29 2018-10-23 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
WO2016053850A1 (en) 2014-09-29 2016-04-07 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
US9889137B2 (en) 2014-09-29 2018-02-13 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
US20160089374A1 (en) * 2014-09-29 2016-03-31 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
US9694013B2 (en) * 2014-09-29 2017-07-04 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
WO2016126798A1 (en) 2015-02-04 2016-08-11 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
US10434105B2 (en) 2015-02-04 2019-10-08 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
US10201543B2 (en) 2015-02-04 2019-02-12 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
US9771341B2 (en) 2015-03-18 2017-09-26 Abide Therapeutics, Inc. Piperazine carbamates and methods of making and using same
US9994537B2 (en) 2015-03-18 2018-06-12 Abide Therapeutics, Inc. Piperazine carbamates and methods of making and using same
US10577329B2 (en) 2015-04-21 2020-03-03 Forma Therapeutics, Inc. Fused-bicyclic aryl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
WO2016171755A1 (en) 2015-04-21 2016-10-27 Forma Therapeutics, Inc. Fused-bicyclic aryl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
EA038574B1 (en) * 2015-04-21 2021-09-16 Форма Терапьютикс, Инк. Pyridin-2(1h)-one quinolinone derivatives and pharmaceutical compositions thereof
US10807976B2 (en) 2015-04-21 2020-10-20 Forma Therapeutics, Inc. Quinolinone five-membered heterocyclic compounds as mutant-isocitrate dehydrogenase inhibitors
WO2016171756A1 (en) * 2015-04-21 2016-10-27 Forma Therapeutics, Inc. Quinolinone five-membered heterocyclic compounds as mutant-isocitrate dehydrogenase inhibitors
US10407419B2 (en) 2015-04-21 2019-09-10 Forma Therapeutics, Inc. Quinolinone five-membered heterocyclic compounds as mutant-isocitrate dehydrogenase inhibitors
US10294206B2 (en) 2015-04-21 2019-05-21 Forma Tm2, Inc. Fused-bicyclic aryl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
US9624216B2 (en) 2015-04-21 2017-04-18 Forma Therapeutics, Inc. Quinolinone five-membered heterocyclic compounds as mutant-isocitrate dehydrogenase inhibitors
WO2016177347A1 (en) * 2015-05-07 2016-11-10 Teligene Ltd Heterocyclic compounds as idh2 inhibitors
US10450302B2 (en) 2015-05-11 2019-10-22 Lundbeck La Jolla Research Center, Inc. Methods of treating inflammation or neuropathic pain
US11034674B2 (en) 2015-05-11 2021-06-15 H. Lundbeck A/S Methods of treating inflammation or neuropathic pain
US11234976B2 (en) 2015-06-11 2022-02-01 Agios Pharmaceuticals, Inc. Methods of using pyruvate kinase activators
US10745383B2 (en) 2015-07-30 2020-08-18 Chia Tai Tianqing Pharmaceutical Group Co., Ltd. 1,3,5-triazine derivative and method of using same
CN108349933A (en) * 2015-08-05 2018-07-31 安吉奥斯医药品有限公司 The method for preparing 6- (aryl or heteroaryl) -1,3,5- triazine -2,4- glycol and 6- (aryl or heteroaryl) -1,3,5- triazine -2,4- diamines
WO2017024134A1 (en) * 2015-08-05 2017-02-09 Agios Pharmaceuticals, Inc. Methods of preparing 6-(aryl or heteroaryl)-1,3,5-triazine-2,4-diols and 6-(aryl or heteroaryl)-1,3,5-triazine-2,4-diamines
US9751863B2 (en) 2015-08-05 2017-09-05 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
US11419859B2 (en) 2015-10-15 2022-08-23 Servier Pharmaceuticals Llc Combination therapy for treating malignancies
US10653710B2 (en) 2015-10-15 2020-05-19 Agios Pharmaceuticals, Inc. Combination therapy for treating malignancies
AU2016340740B2 (en) * 2015-10-21 2018-07-19 NeuForm Pharmaceuticals, Inc. Deuterated compounds for treating hematologic malignancies, and compositions and methods thereof
WO2017069878A1 (en) * 2015-10-21 2017-04-27 NeuForm Pharmaceuticals, Inc. Deuterated compounds for treating hematologic malignancies, and compositions and methods thereof
JP2018531279A (en) * 2015-10-21 2018-10-25 ノイフォルム・ファーマシューティカルズ・インコーポレイテッドＮｅｕｆｏｒｍ Ｐｈａｒｍａｃｅｕｔｉｃａｌｓ， Ｉｎｃ． Deuterium compounds and compositions and methods for treating hematological malignancies
AU2016362425B2 (en) * 2015-12-04 2022-04-21 Les Laboratoires Servier Methods of treatment of malignancies
US10188656B2 (en) 2015-12-04 2019-01-29 Agios Pharmaceuticals, Inc. Methods of treatment of malignancies
WO2017096150A1 (en) * 2015-12-04 2017-06-08 Agios Pharmaceuticals, Inc. Methods of treatment of malignancies
WO2017140758A1 (en) 2016-02-19 2017-08-24 Debiopharm International S.A. Derivatives of 2-amino-4-(2-oxazolidinon-3-yl)-pyrimidine fused with a five-membered heteroaromatic ring in 5,6-position which are useful for the treatment of various cancers
US10463753B2 (en) 2016-02-19 2019-11-05 Lundbeck La Jolla Research Center, Inc. Radiolabeled monoacylglycerol lipase occupancy probe
US10961222B2 (en) 2016-07-21 2021-03-30 Nanjing Sanhome Pharmaceutical Co., Ltd. Chemical compound of isocitrate dehydrogenase inhibitor, and application thereof
US20190161473A1 (en) * 2016-07-21 2019-05-30 Nanjing Sanhome Pharmaceutical Co., Ltd. Chemical compound of isocitrate dehydrogenase inhibitor, and application thereof
WO2018014852A1 (en) * 2016-07-21 2018-01-25 南京圣和药业股份有限公司 Chemical compound of isocitrate dehydrogenase inhibitor, and application thereof
WO2018048847A1 (en) 2016-09-07 2018-03-15 Celgene Corporation Tablet compositions
US10899737B2 (en) 2016-09-19 2021-01-26 Lundbeck La Jolla Research Center, Inc. Piperazine carbamates and methods of making and using same
US9981930B1 (en) 2016-11-16 2018-05-29 Abide Therapeutics, Inc. MAGL inhibitors
US10093635B2 (en) 2016-11-16 2018-10-09 Abide Therapeutics, Inc. MAGL inhibitors
US11021464B2 (en) 2017-01-22 2021-06-01 Chia Tai Tianqing Pharmaceutical Group Co., Ltd. Crystalline forms of 4-(tert-butoxyamino)-6-(6-(trifluoromethyl)pyridin-2-yl)-N-(2-(trifluoromethyl)pyridin-4-yl)-1,3,5-triazin-2-amine methanesulfonic acid salt
US11773079B2 (en) 2017-01-22 2023-10-03 Chia Tai Tianqing Pharmaceutical Group Co, Ltd. Crystalline forms of 4-(tert-butoxyamino)-6-(6-(trifluoromethyl)pyridin-2-yl)-N-(2-(trifluoromethyl)pyridin-4-yl)-1,3,5-triazin-2-amine
US11229653B2 (en) 2017-05-05 2022-01-25 Celgene Corporation Methods of treatment of myeloproliferative neoplasm
US11833154B2 (en) 2017-05-05 2023-12-05 Memorial Sloan Kettering Cancer Center Methods of treatment of myeloproliferative neoplasm
WO2018204787A1 (en) * 2017-05-05 2018-11-08 Memorial Sloan Kettering Cancer Center Methods of treatment of myeloproliferative neoplasm
US11414390B2 (en) 2017-09-07 2022-08-16 Hutchison Medipharma Limited Cycloolefin substituted heteroaromatic compounds and their use
CN110051673A (en) * 2018-01-19 2019-07-26 南京圣和药业股份有限公司 A kind of medical composition and its use comprising triazines IDH inhibitor
US10570106B2 (en) 2018-05-15 2020-02-25 Lundbeck La Jolla Research Center, Inc. MAGL inhibitors
US11332453B2 (en) 2018-05-15 2022-05-17 H. Lundbeck A/S MAGL inhibitors
US11214557B2 (en) 2018-05-15 2022-01-04 H. Lundbeck A/S MAGL inhibitors
US11013734B2 (en) 2018-05-16 2021-05-25 Forma Therapeutics, Inc. Treating patients harboring an isocitrate dehydrogenase-1 (IDH-1) mutation
US11376246B2 (en) 2018-05-16 2022-07-05 Forma Therapeutics, Inc. Inhibiting mutant IDH-1
US10959994B2 (en) 2018-05-16 2021-03-30 Forma Therapeutics, Inc. Solid forms of ((S)-5-((1-(6-chloro-2-oxo-1,2-dihydroquinolin-3-yl)ethyl)amino)-1-methyl-6-oxo-1,6-dihydropyridine-2-carbonitrile
US11576906B2 (en) 2018-05-16 2023-02-14 Forma Therapeutics, Inc. Inhibiting mutant IDH-1
US12053463B2 (en) 2018-05-16 2024-08-06 Forma Therapeutics, Inc. Solid forms of ((s)-5-((1-(6-chloro-2-oxo-1,2-dihydroquinolin-3-yl)ethyl)amino)-1-methyl-6-oxo-1,6-dihydropyridine-2-carbonitrile
US11311527B2 (en) 2018-05-16 2022-04-26 Forma Therapeutics, Inc. Inhibiting mutant isocitrate dehydrogenase 1 (mIDH-1)
US11013733B2 (en) 2018-05-16 2021-05-25 Forma Therapeutics, Inc. Inhibiting mutant isocitrate dehydrogenase 1 (mlDH-1)
US10532047B2 (en) 2018-05-16 2020-01-14 Forma Therapeutics, Inc. Solid forms of ((S)-5-((1-(6-chloro-2-oxo-1,2-dihydroquinolin-3-yl)ethyl)amino)-1-methyl-6-oxo-1,6-dihydropyridine-2-carbonitrile
US11723905B2 (en) 2018-05-16 2023-08-15 Forma Therapeutics, Inc. Solid forms of ((s)-5-((1-(6-chloro-2-oxo-1,2-dihydroquinolin-3-yl)ethyl)amino)-1-methyl-6-oxo-1,6-dihydropyridine-2-carbonitrile
US11738018B2 (en) 2018-05-16 2023-08-29 FORMA Therapeuetics, Inc. Inhibiting mutant isocitrate dehydrogenase 1 (mIDH-1)
US11963956B2 (en) 2018-05-16 2024-04-23 Forma Therapeutics, Inc. Inhibiting mutant isocitrate dehydrogenase 1 (mIDH-1)
US11497743B2 (en) 2018-05-16 2022-11-15 Forma Therapeutics, Inc. Treating patients harboring an isocitrate dehydrogenase 1 (IDH-1) mutation
US10980788B2 (en) 2018-06-08 2021-04-20 Agios Pharmaceuticals, Inc. Therapy for treating malignancies
WO2020092894A1 (en) 2018-11-02 2020-05-07 Celgene Corporation Solid forms of 2-methyl-1-[(4-[6-(trifluoromethyl) pyridin-2-yl]-6-{[2-(trifluoromethyl)pyridin-4-yl]amino}-1,3,5-triazin-2-yl) amino]propan-2-ol
WO2020092906A1 (en) 2018-11-02 2020-05-07 Celgene Corporation Co-crystals of 2-methyl-1 -[(4-[6-(trifluoromethyl)pyridin-2-yl]-6-{[2-(trifluoromethyl) pyridin-4-yl]amino}-1,3,5-triazin-2-yl)amino]propan-2-ol, compositions and methods of use thereof
WO2020092915A1 (en) 2018-11-02 2020-05-07 Celgene Corporation Solid dispersions for treatment of cancer
WO2020239759A1 (en) 2019-05-27 2020-12-03 Sandoz Ag Amorphous enasidenib in a stabilized form
WO2021057975A1 (en) * 2019-09-29 2021-04-01 贝达药业股份有限公司 Mutant idh2 inhibitor and application thereof
CN114502537A (en) * 2019-09-29 2022-05-13 贝达药业股份有限公司 Mutant IDH2 inhibitor and application thereof
WO2021097160A1 (en) 2019-11-14 2021-05-20 Celgene Corporation Pediatric formulations for treatment of cancer
US11702393B2 (en) 2020-04-21 2023-07-18 H. Lundbeck A/S Synthesis of a monoacylglycerol lipase inhibitor
WO2023183520A1 (en) * 2022-03-24 2023-09-28 A2A Pharmaceuticals, Inc. Compositions and methods for treating cancer
US11986475B1 (en) 2022-03-24 2024-05-21 A2A Pharmaceuticals, Inc. Compositions and methods for treating cancer
RU2791798C1 (en) * 2022-12-29 2023-03-13 Федеральное государственное бюджетное учреждение "Российский научный центр радиологии и хирургических технологий имени академика А.М. Гранова" Министерства здравоохранения Российской Федерации Methyl 6-[(4-(aziridin-1-yl)-6-chloro-1,3,5-triazin-2-yl)amino]hexanoate, which has a cytotoxic effect

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