OA18771A - Imidazopyrazinones as PDE1 Inhibitors - Google Patents
Imidazopyrazinones as PDE1 Inhibitors Download PDFInfo
- Publication number
- OA18771A OA18771A OA1201700409 OA18771A OA 18771 A OA18771 A OA 18771A OA 1201700409 OA1201700409 OA 1201700409 OA 18771 A OA18771 A OA 18771A
- Authority
- OA
- OAPI
- Prior art keywords
- methyl
- pyrazin
- imidazo
- pyran
- tetrahydro
- Prior art date
Links
- 101700084262 PDE1C Proteins 0.000 title abstract description 47
- 230000002401 inhibitory effect Effects 0.000 title abstract description 35
- 239000003112 inhibitor Substances 0.000 title abstract description 26
- MPWOBEOETVOESI-UHFFFAOYSA-N imidazo[4,5-b]pyrazin-2-one Chemical class N1=CC=NC2=NC(=O)N=C21 MPWOBEOETVOESI-UHFFFAOYSA-N 0.000 title abstract description 4
- SLYRIXNICMCXFH-UHFFFAOYSA-N 7H-imidazo[1,5-a]pyrazin-8-one Chemical compound O=C1NC=CN2C=NC=C12 SLYRIXNICMCXFH-UHFFFAOYSA-N 0.000 claims description 118
- 150000001875 compounds Chemical class 0.000 claims description 112
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 48
- 125000000217 alkyl group Chemical group 0.000 claims description 40
- 125000001424 substituent group Chemical group 0.000 claims description 28
- -1 bicyclic ethers Chemical class 0.000 claims description 25
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 25
- 239000011737 fluorine Chemical group 0.000 claims description 21
- 229910052731 fluorine Inorganic materials 0.000 claims description 21
- 238000007792 addition Methods 0.000 claims description 20
- YCKRFDGAMUMZLT-UHFFFAOYSA-N fluorine atom Chemical group [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims description 20
- 229910052739 hydrogen Inorganic materials 0.000 claims description 17
- 239000001257 hydrogen Substances 0.000 claims description 17
- 239000011780 sodium chloride Substances 0.000 claims description 17
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- 150000003839 salts Chemical class 0.000 claims description 16
- 229910052736 halogen Inorganic materials 0.000 claims description 15
- 150000002367 halogens Chemical group 0.000 claims description 15
- 125000006163 5-membered heteroaryl group Chemical group 0.000 claims description 14
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 9
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 9
- 125000003566 oxetanyl group Chemical group 0.000 claims description 9
- 125000004432 carbon atoms Chemical group C* 0.000 claims description 8
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 7
- 125000003545 alkoxy group Chemical group 0.000 claims description 6
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 6
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims description 6
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 6
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- MIPHRQMEIYLZFZ-UHFFFAOYSA-N oxolan-3-amine Chemical group NC1CCOC1 MIPHRQMEIYLZFZ-UHFFFAOYSA-N 0.000 claims description 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 4
- KAESVJOAVNADME-UHFFFAOYSA-N pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims description 4
- 125000001412 tetrahydropyranyl group Chemical group 0.000 claims description 4
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- HCHKCACWOHOZIP-UHFFFAOYSA-N zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N β-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
Abstract
The present invention provides imidazopyrazinones as PDE1 inhibitors and their use as a medicament, in particular for the treatment of neurodegenerative disorders and psychiatrie disorders.
Description
Imidazopyrazinones as PDE1 Inhibitors
FIELD OF THE INVENTION
The présent invention provides compounds that are PDE1 enzyme inhibitors and their use as a médicament, in particular for the treatment of neurodegenerative disorders and psychiatrie disorders. The présent invention also provides pharmaceutical compositions comprising compounds of the invention and methods of treating disorders using the compounds of the invention.
BACKGROUND OF THE INVENTION
Throughout this application, various publications are referenced in full. The disclosures of these publications are hereby incorporated by reference into this application to describe more fully the state ofthe art to which this invention pertains.
The second messenger cyclic Nucléotides (cNs), cyclic adenosine monophosphate (cAMP) and cyclic guanosine monophosphate (cGMP) play a major rôle in intracellular signal transduction cascade, by regulating cN-dependent protein kinases (PKA and PKG), EPACs (Exchange Protein Activated by cAMP), phosphoprotein phosphatases, and/or cN-gated cation channels. In neurons, this includes the activation of cAMP- and cGMP-dependent kinases and subséquent phosphorylation of proteins involved in acute régulation of synaptic transmission as well as in neuronal différentiation and survival. Intracellular concentrations of cAMP and cGMP are strictly regulated by the rate of biosynthesis by cyclases and by the rate of dégradation by phosphodiesterases (PDEs, EC 3.1.4.17). PDEs are bimetallic hydrolases that inactivate cAMP/cGMP by catalytic hydrolysis of the 3’-ester bond, forming the inactive 5’-monophosphate. Since PDEs provide the only means of degrading the cyclic nucléotides cAMP and cGMP in cells, PDEs play an essential rôle in cyclic nucléotide signalling. The catalytic activities of PDEs provide for breakdown of cNs over a spectrum of cN-concentrations in ail cells, and their varied regulatory mechanisms provide for intégration and crosstalk with myriads of signalling pathways. Particular PDEs are targeted to discrète compartments within cells where they control cN level and sculpt microenvironments for a variety of cN signalosomes (Sharron H. Francis, Mitsi A. Blount, and Jackie D. Corbin. Physiol Rev 2011,91: 651-690).
On the basis of substrate specificity, the PDE families can be divided into three groups: 1) The cAMP-specific PDEs, which inciude PDE4, PDE7, and PDE8, 2) the cGMP-selective enzymes PDE5 and PDE9, and 3) the dual-substrate PDEs, PDE1, PDE2, PDE3, as well as PDE10 and PDE11.
Previousiy named calmodulin-stimulated PDE (CaM-PDE), PDE1 is unique in that it is Ca2+dependently regulated via calmodulin (CaM. a 16 kDa Ca2*-binding protein) complexed with four Ca2+ (for review, Sharron H. Francis, Mitsi A. Blount, and Jackie D. Corbin. Physiol Rev 2011, 91: 651-690). Thus, PDE1 represents an interesting regulatory link between cyclîc nucléotides and intracellular Ca2*. The PDE1 family is encoded by three genes: PDE1A (mapped on human chromosome 2q32), PDE1B (human chromosome location, hcl: 12q13) and PDE1C (hcl: 7p14.3). They hâve alternative promoters and give rise to a multitude of proteins by alternative splicing which differ in their regulatory properties, substrate affinities, spécifie activities, activation constants for CaM, tissue distribution and molecular weights. More than 10 human isoforms are identified. Their molecular weights vary from 58 to 86 kDa per monomer. The N-terminal regulatory domain that contains two Ca2+/CaM binding domains and two phosphorylation sites differentiate their corresponding proteins and modulate their biochemical functions. PDE1 is a dual substrate PDE and the PDE1Csubtype has equal activity towards cAMP and cGMP (Km = 1-3 μΜ), whereas the subtypes PDE1A and PDE1B hâve a preference for cGMP (Km for cGMP = 1-3 μΜ and for cAMP = 10-30 μΜ).
The PDE1 subtypes are highly enriched in the brain and located especially in the striatum (PDE1B), hippocampus (PDE1A) and cortex (PDE1A) and this localization is conserved across species (Amy Bernard et al. Neuron 2012, 73, 1083-1099). In the cortex, PDE1A is présent mainly in deep cortical layers 5 and 6 (output layers), and used as a specificity marker for the deep cortical layers. PDE1 inhibitors enhance the levels of the second messenger cNs leading to enhanced neuronal excitability.
Thus, PDE1 is a therapeutic target for régulation of intracellular signaling pathways, preferably in the nervous system and PDE1 inhibitors can enhance the levels of the second messengers cAMP/cGMP leading to modulation of neuronal processes and to the expression of neuronal plasticity-related genes, neurotrophic factors, and neuroprotective molécules. These neuronal plasticity enhancement properties together with the modulation of synaptic transmission make PDE1 inhibitors good candidates as therapeutic agents in many neurological and psychiatrie conditions. The évaluation of PDE1 inhibitors in animal models (for reviews see e.g. Blokland et al. Expert Opinion on Therapeutic Patents (2012),
22(4), 349-354; and Médina, A. E. Frontiers in Neuropharmacology (2011), 5(Feb.), 21) has suggested the potential for the therapeutic use of PDE1 inhibitors in neurological disorders, like e.g. Alzheimer’s, Parkinson's and Huntington's Diseases and in psychiatrie disorders like e.g. Attention Déficit hyperactivity Disorder (ADHD), restless leg syndrome, dépréssion, anxiety, narcolepsy, cognitive impairment and cognitive impairment associated with schizophrenia (CIAS). There hâve also been patent applications claiming that PDE1 inhibitors are useful in diseases that may be alleviated by the enhancement of progesteronesignaltng such as female sexual dysfunction (e.g. WO 2008/070095).
WO 2013/053690 A1 discloses imidazopyrazinones that are inhibitors of the PDE9 enzyme.
The compounds of the invention may offer alternatives to current marketed treatments for neurodegenerative and/or psychiatrie disorders, treatments which are not efficacious in all patients. Hence, there remains a need for alternative methods of treatment of such diseases.
SUMMARY OF THE INVENTION
PDE1 enzymes are expressed in the Central Nervous System (CNS), making this gene family an attractive source of new targets for the treatment of psychiatrie and neurodegenerative disorders.
The objective of the présent invention is to provide compounds that are PDE1 inhibitors, and as such are useful to treat neurodegenerative disorders and psychiatrie disorders.
Preferrably, said compounds are at least a ten-fold stronger as PDE1 inhibitors than as PDE9 inhibitors in order to prevent potentially unwanted effects associated with PDE9 inhibition.
Accordingly, the present invention relates to compounds of formula (I)
(I) wherein n is 0 or 1;
q is 0 or 1;
R1 is selected from the group consisting of benzyl, indanyl, indoline and 5-membered heteroaryls; ail of which can be substituted with a substituent selected from the group consisting of halogen and C,-C3 alkyl; or
R1 is selected from the group consisting of saturated monocyclic rings containing 4-6 carbon atoms and 1-2 nitrogen atoms; ail of which can be substituted one or more times with one or more substituents selected from the group consisting of methyl, fluorine and sulfonamide, or
R1 is selected from the group consisting of lactams containing 4-6 carbon atoms; ail of which can be substituted one or more times with one or more substituents selected from the group consisting of methyl and fluorine; or
R1 is selected from the group consisting of bicyclic ethers such as, 7oxabicyclo[2.2.1]heptane; ail of which can be substituted one or more times with one or more substituents selected from the group consisting of methyl and fluorine; or
R1 is selected from the group consisting of linear or branched Ο,-Ο8 alkyl, saturated monocyclic C3-Ca cycloalkyl, oxetanyl, tetrahydrofuranyl and tetrathydropyranyl; ail of which can be substituted one or more times with one or more substituents selected from the group consisting of methyl, fluorine, hydroxy, cyano or methoxy; or
R1 is a linear or branched C,-C3 alkyl, which is substituted with a substituent selected from phenyl and 5-membered heteroaryl, wherein said 5-membered heteroaryl can be substituted with one or more CrC3 alkyls; or
R1 is selected from the group consisting of morpholine, tetrahydrofuran-3-amine, hexahydro2/7-furo[3,2-b]pyrrole and homomorpholine; ail of which can be subsîtuted with one or more substituents selected from the group consisting of Ο,-Ο3 alkyl;
R2 is selected from the group consisting of hydrogen, linear or branched ΟΊ-Ο8 alkyl, phenyl, saturated monocyclic C3-C8 cycloalkyl, oxetanyl, benzo[c/][1,3]dioxolyI, tetrahydrofuranyl and tetrahydropyranyl; or
R2 is phenyl or pyridyi substituted with one or more substituents selected from the group consisting of hydroxyl, amino, cyano, halogen, CrC3 alkyl, Ο,-Ο3 alkoxy, C3-C5 cydoalkoxy, C3-C5 cycloalkyl-methoxy, Ο,-Ο3 fluoroalkoxy, and -NC(O)CH3; or
R2 is a 5-membered heteroaryl which can be substituted one or more times with Ci-C3 alkyl;
R3 is selected from the group consisting of hydrogen, halogen, CrCs alkyl, C3-C5 cycloalkyl and phenyl; or
R3 is selected from the group consisting of phenyl substituted one or more times with C,-C3 alkyl; methyl substituted one, two or three times with fluorine; ethyl substituted one, two or three times with fluorine;
R4 is hydrogen;
and tautomers and pharmaceutically acceptable addition salts thereof;
with the proviso that R2 and R3 cannot be hydrogen at the same time;
with the proviso, that the compound of formula (I) is not one of the three following compounds:
3-methyl-7-(4-(trifluoromethoxy)benzyl)imidazo[1,5-a]pyrazin-8(7H)-one;
7-butyl-3-methylimidazo[1,5-a]pyrazin-8(7F/)-one; and
7-(4-methoxybenzyl)-3-methylimidazo[1,5-a]pyrazin-8(7H)-one.
Reference to Compound I includes the free base of Compound I, pharmaceutically acceptable salts of Compound I, such as acid addition salts of Compound I, racemic mixtures of Compound I, or the corresponding enantiomer and/or optical isomer of Compound I, and polymorphie and amorphic forms of Compound I as well as tautomeric forms of Compound I. Furthermore, the compounds of this invention may exist in unsolvated as well as in solvated forms with pharmaceutically acceptable solvents such as water, éthanol and the like. In general, the solvated forms are considered équivalent to the unsolvated forms for the purposes of this invention.
In one embodiment, the invention relates to a compound according to formula (I) for use in therapy.
In one embodiment, the invention relates to a compound according to formula (I), for use in the treatment of a neurodegenerative disorder, selected from the group consisting of Alzheimer's Disease, Parkinson's Disease and Huntington's Disease or for the treatment of a psychiatrie disorder such as Attention Déficit hyperactivity Disorder (ADHD), dépréssion, anxiety, narcolepsy, cognitive impairment and cognitive impairment associated with schizophrenia (CIAS), or another brain disease like restless leg syndrome.
In one embodiment, the invention relates to a pharmaceutical composition comprising a compound according formula (I), and one or more pharmaceutically acceptable carrier or excipient.
In one embodiment, the invention relates to a method for the treatment of a neurodegenerative disorder, selected from the group consisting of Alzheimeris Disease, Parkinson's Disease and Huntington's Disease or for the treatment of a psychiatrie disorder such as Attention Déficit hyperactivity Disorder (ADHD), dépression, anxîety, narcolepsy, cognitive impairment and cognitive impairment associated with schizophrenia (CIAS), or another brain disease like restless leg syndrome, which method comprises the administration of a therapeutically effective amount of a compound according to formula (I) to a patient in need thereof.
DETAILED DESCRIPTION OF THE INVENTION
EMBODIMENTS OF THE INVENTION
The following notation is applied: an embodiment of the invention is identified as Ei, where i is an integer indicating the number of the embodiment. An embodiment Ei' specifying a spécifie embodiment a previously listed embodiment Ei is identified as Ei’(Ei), e.g. E2(E1) means “in an embodiment E2 of embodiment E1”.
Where an embodiment is a combination of two embodiments the notation is similarly Ei(Ei and Ei’), e.g. E3(E2 and E1) means “in an embodiment E3 of any of embodiments E2 and ΕΓ
Where an embodiment is a combination of more than two embodiments the notation is similarly Ei’(Ei, Ei' and Ei”), e.g. E4(E1, E2 and E3) means “in an embodiment E4 of any of embodiments E1, E2 and E3”
In a first embodiment E1, the présent invention relates to compounds of formula (I) (l) wherein n is O or 1;
q is 0 or 1 ;
R1 is selected from the group consisting of benzyl, indanyl, indoline and 5-membered heteroaryls; ail of which can be substituted with a substituent selected from the group consisting of halogen and CrC3 alkyl; or
R1 is selected from the group consisting of saturated monocycîic rings containing 4-6 carbon atoms and 1-2 nitrogen atoms; ail of which can be substituted one or more times with one or more substituents selected from the group consisting of methyl, fluorine and sulfonamide; or
R1 is selected from the group consisting of lactams containing 4-6 carbon atoms; ail of which can be substituted one or more times with one or more substituents selected from the group consisting of methyl and fluorine; or
R1 is selected from the group consisting of bicyclic ethers such as, 7oxabicyclo[2.2.1]heptane; ail of which can be substituted one or more times with one or more substituents selected from the group consisting of methyl and fluorine; or
R1 is selected from the group consisting of linear or branched Ci-C8 alkyl, saturated monocycîic C3-C8 cycloalkyl, oxetanyl, tetrahydrofuranyï and tetrathydropyranyl; ail of which can be substituted one or more times with one or more substituents selected from the group consisting of methyl, fluorine, hydroxy, cyano or methoxy; or
R1 is a linear or branched C-i-C3 alkyl, which is substituted with a substituent selected from phenyl and 5-membered heteroaryl, wherein said 5-membered heteroaryl can be substituted with one or more CtC3 alkyls; or
R1 is selected from the group consisting of morpholine, tetrahydrofuran-3-amine, hexahydro2/7-furo[3,2-b]pyrrole and homomorpholine; ail of which can be subsituted with one or more substituents selected from the group consisting of Ci-C3 alkyl;
R2 is selected from the group consisting of hydrogen, linear or branched C,-C8 alkyl, phenyl, saturated monocycîic C3-Ce cycloalkyl, oxetanyl, benzo[cf][1,3]dioxolyl, tetrahydrofuranyï and tetrahydropyranyï; or
R2 is phenyl or pyridyl substituted with one or more substituents selected from the group consisting of hydroxyl, amino, cyano, halogen, C^Ca aikyl, Ct-C3 alkoxy, C3-C5 cycloalkoxy, C3-C5 cycloalkyl-methoxy, C^-Ca fluoroalkoxy, and -NC(O)CH3; or
R2 is a 5-membered heteroaryl which can be substituted with one or more CrC3 aikyl;
R3 is selected from the group consisting of hydrogen, halogen, C-rC5 aikyl, C3-C5 cycîoalkyl and phenyl; or
R3 is selected from the group consisting of phenyl substituted one or more times with CVC3 aikyl; methyl substituted one, two or three times with fluorine; ethyl substituted one, two or three times with fluorine;
R4 is hydrogen;
and tautomers and pharmaceutically acceptable addition salts thereof;
with the proviso that R2 and R3 cannot be hydrogen at the same time;
with the proviso, that the compound of formula (I) is not one ofthe three following compounds:
3-methyl-7-(4-(trifluoromethoxy)benzyl)imidazo[1,5-a]pyrazin-8(7/-/)-one;
7-butyl-3-methylimidazo[1,5-a]pyrazin-8(7/-/)-one; and
7-(4-methoxybenzyl)-3-methylimidazo[1,5-a]pyrazin-8(7H)-one,
E2(E1) n is 0 or 1;
q is 0 or 1;
R1 is selected from the group consisting of linear or branched CrC8 aikyl, saturated monocyclic C3-C8 cycîoalkyl, oxetanyl, tetrahydrofuranyï, and tetrathydropyranyï,
R2 is selected from the group consisting of, linear or branched C^Ce aikyl, phenyl, and saturated monocyclic C3-Cs cycîoalkyl; or
R2 is selected from the group consisting of phenyl substituted with one or more times with one or more substituents selected from the group consisting of halogen, CrC3 aikyl and methoxy;
R3 is selected from the group consisting of hydrogen, CrC3 alkyl, halogen and benzyl;
R.-. is hydrogen.
E3(E1 or E2) R1 is tetrahydropyranyl.
E4(E1 or E2) R1 is C,-C3 alkyl or C3-C5 cycloalkyl.
E5(E4) R1 is propyl or cyclopropyl
E6(E1 to E5) R2 is phenyl.
E7(E1 to E5) R2 is substituted phenyl, wherein the one or more substituents are selected from the group consisting of fluorine, chlorine, methyl and methoxy.
E8(E1 to E5) R2 is saturated monocyclic C3-C8 cycloalkyl.
E9(E1 and E8) R2 is saturated monocyclic C5-C7 cycloalkyl.
E10(E1 to E5) R2 is CrC3 alkyl.
E11(E1 and E10) R2 is methyl, ethyl or isopropyl
E12(E1 to E11) R3 is bromine
E13(E1 to E11) R3 is methyl
E14(E1 to E11) R3 is selected from hydrogen and methyl; and
R2 is selected from the group consisting of linear or branched C-i-C8 alkyl, phenyl, saturated monocyclic C3-C8 cycloalkyl, oxetanyl, tetrahydrofuranyl and tetrahydropyranyl; or
R2 is phenyl or pyridyl substituted with one or more substituents selected from the group consisting of hydroxyl, amino, cyano, halogen, C^Cs alkyl, CrC3 alkoxy, C-|-C3 fluoroalkoxy, and -NC(O)CH3; or
R2 is a 5-membered heteroaryl which can be substituted with Ci-C3 alkyl.
E15(E1 to E14) n is 0.
E16(E1 to E14) n is 1.
E17(E1 to E15) q is 0.
E18(E1 to E15)q is 1.
E19(E1), the compound of formula (I) is selected among the compounds listed in Table 1, in the form of the free base, one or more tautomers thereof or a pharmaceutically acceptable sait thereof.
E20(E1 to E19) the compound has a PDE1A, PDE1B orPDEIC IC50 value, determined as described in the section “PDE1 inhibition assay, of 10 micro molar or less, such as 5 micro molar or less, such as 4 micro molar or less. such as 3 micro molar or less, such as 2 micro molar or less, such as 1 micro molar or less, such as 500 nM or less, such as 400 nM or less, such as 300 nM or less, such as 200 nM or less, such as 100 nM or less.
E21(E1) the compound is selected from the compounds listed in Table 1 and pharmaceutically acceptable salts thereof.
E22(E1 to E21) the compound is at least 10 times stronger PDE1 inhibitors than PDE9 inhibitors, such as at least 50 times stronger PDE1 inhibitors than PDE9 inhibitors or even at least 100 times stronger PDE1 inhibitors than PDE9 inhibitors.
E23(E1 to E22) the compound is for use as a médicament.
E24(E1 to E22) the compound is for use in the treatment of AttentionDeficit hyperactivity Disorder (ADHD).
E25(E1 to E22) a pharmaceutical composition comprising a therapeutically effective amount of a compound of any of embodiments (E1) to (E22), and one or more pharmaceutically acceptable carriers, diluents and excipients.
E26(E25) the pharmaceutical composition is for the treatment of neurodegenerative disorder, selected from the group consisting of Alzheimer's Disease, Parkinson's Disease and Huntingtoris Disease or for the treatment of a psychiatrie disorder such as Attention Déficit hyperactivity Disorder (ADHD), dépréssion, anxiety, narcolepsy, cognitive impairment and cognitive impairment associated with schtzophrenia (CIAS) or another brain disease like restless leg syndrome.
E27(E1 to E22) a compound of any of embodiments (E1) to (E22) for use in the treatment of a neurodegenerative disorder, selected from the group consisting of Alzheimer's Disease, Parkinson's Disease and Huntingtoris Disease or for the treatment of a psychiatrie disorder such as Attention Déficit hyperactivity Disorder (ADHD), dépréssion, anxiety, narcolepsy, cognitive impairment and cognitive impairment associated with schizophrenia (CIAS) or another brain disease like restless leg syndrome.
E28(E 1 to E22) a method of treating a subject suffering from neurodegenerative disorder, selected from the group consisting of Alzheimer’s Disease, Parkinson's Disease and Huntington's Disease or for the treatment of a psychiatrie disorder such as Attention Déficit hyperactivity Disorder (ADHD), dépression, anxiety, narcolepsy, cognitive impairment and cognitive impairment associated with schizophrenia (CIAS) or another brain disease like restless leg syndrome, which method comprises administering to said subject an amount of a compound of formula I effective in inhibiting PDE1.
E29 (E1 to E22) Use of a compound of any of embodiments (E1) to (E21) in the manufacture of a médicament for use in the treatment of a neurodegenerative disorder, selected from the group consisting of Alzheimer’s Disease, Parkinson's Disease and Huntington’s Disease or for the treatment of a psychiatrie disorder such as Attention Déficit hyperactivity Disorder (ADHD), dépréssion, anxiety, narcolepsy, cognitive impairment and cognitive impairment associated with schizophrenia (CIAS) or another brain disease like restless leg syndrome.
DEFINITIONS
PDE1 ENZYMES
The PDE1 isozyme family includes numerous splice variant PDE1 isoforms. It has three subtypes, PDE1A, PDE1B and PDE1C which divide further into various isoforms. In the context of the present invention PDE1 and PDE1 enzymes are synonymous and refer to PDE1A, PDE1B and PDE1C enzymes as well as their isoforms unless otherwise specified.
SUBSTITUENTS
As used in the context ofthe present invention, the terms “halo” and “halogen are used interchangeably and refer to fluorine, chlorine, bromine or iodine.
A given range may interchangeably be indicated with (dash) or “to”, e.g. the term C^Cs alkyl” is équivalent to C, to C3 alkyl”.
The terms ”CrC3 alkyl”, C,-^ alkyl”, CrCs alkyl”, CrCe alkyl”, CrCy alkyl” and ”CrC8 alkyl” refer to a linear (i.e. unbranched) or branched saturated hydrocarbon having from one up to eight carbon atoms, inclusive. Examples of such groups include, but are not limited to, methyl, ethyl, 1-propyl, 2-propyl, 1 -butyl, 2-butyl, 2-methyl-2-propyi, 2-methyl-1-butyl, nhexyl, n-heptyl and n-octyl.
The term saturated monocyclic C3-C8 cycloalkyl refers to cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and cyclooctyl. The term C3-C5 cycloalkyl refers to cyclopropyl, cyclobutyl and cyclopentyl.
The term CrC3 alkoxy refers to a moiety of the formula -OR', wherein R’ indicates Ci-C3 alkyl as defined above. The term UC3-C5 cycloalkoxy refers to a moiety of the formula -OR', wherein R' indicates C3-C5 cycloalkyl as defined above. The term “C3-C5 cycloalkyl-methoxy refers to a moiety of the formula -OCH2R', wherein R' indicates C3-C5 cycloalkyl as defined above. Ci-C3 fluoroalkoxy refers to a Ο-03 alkoxy substituted with one or more fluorine.
5-membered heteroaryls are defined as 5 membered aromatic rings containing at least one atom selected frin nitrogen, sulfur and oxygen. Examples include, but are not limited to thiazole, thiophene and isoxazole.
The term lactams containing 4-6 carbon atoms refers to pyrrolidin-2-one, piperidin-2-one or azepan-2-one
ISOMERIC FORMS
Where compounds of the present invention contain one or more chiral centers reference to any of the compounds will, unless otherwise specified, cover the enantiomerically or diastereomerically pure compound as well as mixtures ofthe enantiomers or diastereomers in any ratio.
The above also applies where compounds of the invention contain more than two chiral centers.
PDE1 INHIBITORS AND PDE9 INHIBITORS
In the context ofthe present invention a compound is considered to be a PDE1 inhibitor if the amount required to reach the IC50 level of one or more ofthe three PDE1 isoforms is 10 micro molar or less, preferably less than 9 micro molar, such as 8 micro molar or less, such as 7 micro molar or less, such as 6 micro molar or less, such as 5 micro molar or less, such as 4 micro molar or less, such as 3 micro molar or less, more preferably 2 micro molar or less, such as 1 micro molar or less, in particular 500 nM or less. In preferred embodiments the required amount of PDE1 inhibitor required to reach the IC50 level of PDE1B is 400nM or less, such as 300 nM or less, 200nM or less, 100 nM or less, or even 80 nM or less, such as 50 nM or less, for example 25 nM or less.
In a preferred embodiment the compounds of the présent invention are at least a ten-fold stronger as PDE1 inhibitors as PDE9 inhibitors, i.e. the amount of the compound required to reach the ICg0 level of one or more of the three PDE1 isoforms is at least a ten-fold less than the amount of the same compound required to reach the IC5c level of the PDE9 enzyme.
PHARMACEUTICALLY ACCEPTABLE SALTS
The présent invention also comprises salts of the compounds, typically, pharmaceutically acceptable salts. Such salts include pharmaceutically acceptable acid addition salts. Acid addition salts include salts of inorganic acids as well as organic acids.
Représentative examples of suitable inorganic acids include hydrochloric, hydrobromic, hydroiodic, phosphoric, sulfuric, sulfamic, nitric acids and the like. Représentative examples of suitable organic acids include formic, acetic, trichloroacetic, trifluoroacetic, propionic, benzoic, cinnamic, citric, fumaric, glycolic, itaconic, lactic, methanesulfonic, maleic, malic, malonic, mandelic, oxalic, picric, pyruvic, salicylic, succinic, methane sulfonic, ethanesulfonic, tartaric, ascorbic, pamoic, bismethylene salicylic, ethanedisulfonic, gluconic, citraconic, aspartic, stearic, palmitic, EDTA, glycolic, p-aminobenzoic, glutamic, benzenesulfonic, p-toluenesulfonic acids, theophylline acetic acids, as well as the 8halotheophyllines, for example 8-bromotheophylline and the like. Further examples of pharmaceutically acceptable inorganic or organic acid addition salts include the pharmaceutically acceptable salts listed in Berge, S.M. et al., J. Pharm. Soi. 1977, 66, 2, the contents of which are hereby incorporated by reference.
Furthermore, the compounds of this invention may exist in unsolvated as well as in solvated forms with pharmaceutically acceptable solvents such as water, éthanol and the like. In general, the solvated forms are considered équivalent to the unsolvated forms for the purposes of this invention.
THERAPEUTICALLY EFFECTIVE AMOUNT
In the présent context, the term therapeutically effective amount of a compound means an amount sufficient to cure, alleviate or partially arrest the clinical manifestations of a given disease and its complications in a therapeutic intervention comprising the administration of said compound. An amount adéquate to accomplish this is defined as therapeutically effective amount. Effective amounts for each purpose will dépend on the severity of the disease or injury as well as the weight and general state of the subject. It will be understood that determining an appropriate dosage may be achieved using routine expérimentation, by constructing a matrix of values and testing different points in the matrix, which is ail within the ordinary skills of a trained physician.
In the present context, the term treatment and treating means the management and care □f a patient for the purpose of combating a condition, such as a disease or a disorder. The term is intended to include the full spectrum of treatments for a given condition from which the patient is suffering, such as administration ofthe active compound to alleviate the symptoms or complications, to delay the progression of the disease, disorder or condition, to alleviate or relief the symptoms and complications, and/or to cure or eliminate the disease, disorder or condition as well as to prevent the condition, wherein prévention is to be understood as the management and care of a patient for the purpose of combating the disease, condition, or disorder and includes the administration of the active compounds to prevent the onset of the symptoms or complications. Nonetheless, prophylactic (préventive) and therapeutic (curative) treatments are two separate aspects of the invention. The patient to be treated is preferably a mammal, in particular a human being.
PHARMACEUTICAL COMPOSITIONS
The present invention further provides a pharmaceutical composition comprising a therapeutically effective amount of a compound of formula (I) and a pharmaceutically acceptable carrier or diluent. The present invention also provides a pharmaceutical composition comprising a therapeutically effective amount of one of the spécifie compounds disclosed in the Experimental Section herein and a pharmaceutically acceptable carrier or diluent.
The compounds ofthe invention may be administered alone or in combination with pharmaceutically acceptable carriers, diluents or excipients, in either single or multiple doses. The pharmaceutical compositions according to the invention may be formulated with pharmaceutically acceptable carriers or diluents as well as any other known adjuvants and excipients in accordance with conventional techniques such as those disclosed in
Remington: The Science and Practice of Pharmacy, 21st Edition, Gennaro, Ed., Mack Publishing Co., Easton, PA, 2005.
The pharmaceutical compositions may be specifically formulated for administration by any suitable route such as oral, rectal, nasal, pulmonary, topical (including buccal and sublingual), transdermal and parentéral (including subcutaneous, intramuscular and intravenous) routes It will be appreciated that the route will dépend on the general condition and âge ofthe subject to be treated, the nature ofthe condition to be treated and the active ingrédient.
Pharmaceutical compositions for oral administration include solid dosage forms such as capsules, tablets, dragees, pills, lozenges, powders and granules. Where appropriate, the compositions may be prepared with coatings such as enteric coatings or they may be formulated so as to provide controlled release of the active ingrédient such as sustained or prolonged release according to methods well known in the art. Liquid dosage forms for oral administration include solutions, émulsions, suspensions, syrups and élixirs.
Pharmaceutical compositions for parentéral administration include stérile aqueous and nonaqueous injectable solutions, dispersions, suspensions or émulsions as well as stérile powders to be reconstituted in stérile injectable solutions or dispersions prior to use. Other suitable administration forms include, but are not limited to, suppositories, sprays, ointments, creams, gels, inhalants, dermal patches and implants.
Typical oral dosages range from about 0.001 to about 100 mg/kg body weight per day. Typical oral dosages also range from about 0.01 to about 50 mg/kg body weight per day. Typical oral dosages further range from about 0.05 to about 10 mg/kg body weight per day. Oral dosages are usually administered in one or more dosages, typically, one to three dosages per day. The exact dosage will dépend upon the frequency and mode of administration, the sex, âge, weight and general condition of the subject treated, the nature and severity of the condition treated and any concomitant diseases to be treated and other factors évident to those skilled in the art.
The formulations may also be presented in a unit dosage form by methods known to those skilled in the art. For illustrative purposes, a typical unit dosage form for oral administration may contain from about 0.01 to about 1000 mg, from about 0.05 to about 500 mg, or from about 0.5 mg to about 200 mg.
The present invention also provides a process for making a pharmaceutical composition comprising mixing a therapeutically effective amount of a compound of formula (I) and at least one pharmaceutically acceptable carrier or diluent. In an embodiment, of the présent invention, the compound utilized in the aforementioned process is one of the spécifie compounds disclosed in the Experimental Section herein.
The compounds of this invention are generally utilized as the free substance or as a pharmaceutically acceptable sait thereof. One example is an acid addition sait of a compound which has the same utility as of a free base. When a compound of formula (I) contains a free base such salts are prepared in a conventional manner by treating a solution or suspension of a free base of formula (I) with a pharmaceutically acceptable acid. Représentative examples of suitable organic and inorganic acids are described above.
For parentéral administration, solutions of the compounds of formula (I) in stérile aqueous solution, aqueous propylene glycol or sesame or peanut oil may be employed. Such aqueous solutions should be suitably buffered if necessary and the liquid diluent first rendered isotonie with sufficient saline or glucose. The aqueous solutions are particularly suitable for intravenous, intramuscular, subeutaneous and intraperitoneal administration. The compounds of formula (I) may be readily incorporated into known stérile aqueous media using standard techniques known to those skilled in the art.
Suitable pharmaceutical carriers include inert solid diluents or fillers, stérile aqueous solutions and various organic solvents. Examples of solid carriers include lactose, terra alba, sucrose, cyclodextrin, talc, gelatin, agar, pectin, acacia, magnésium stéarate, stearic acid and lower alkyl ethers of cellulose. Examples of liquid carriers include, but are not limited to, syrup, peanut oil, olive oil, phospholipids, fatty acids, fatty acid amines, polyoxyethylene and water. Similarly, the carrier or diluent may include any sustained release material known in the art, such as glyceryl monostearate or gîyceryl distearate, alone or mixed with a wax. The pharmaceutical compositions formed by combining the compounds of formula (I) and a pharmaceutically acceptable carrier are then readily administered in a variety of dosage forms suitable for the disclosed routes of administration. The formulations may conveniently be presented in unit dosage form by methods known in the art of pharmacy.
Formulations of the present invention suitable for oral administration may be presented as discrète units such as capsules or tablets, each containing a predetermined amount of the active ingrédient, and optionally a suitable excipient. Furthermore, the orally available formulations may be in the form of a powder or granules, a solution or suspension in an aqueous or non-aqueous liquid, or an oil-in-water or water-in-oîl liquid émulsion.
If a solid carrier is used for oral administration, the préparation may be tableted, placed in a hard gelatin capsule in powder or pellet form or it may be in the form of a troche or lozenge. The amount of solid carrier will vary widely but will range from about 25 mg to about 1 g per dosage unit. If a liquid carrier is used, the préparation may be in the form of a syrup, émulsion, soft gelatin capsule orsterile injectable liquid such as an aqueous or non-aqueous liquid suspension or solution.
The pharmaceutical compositions of the invention may be prepared by conventional methods in the art. For example, tablets may be prepared by mixing the active ingrédient with ordinary adjuvants and/or diluents and subsequently compressing the mixture in a conventional tableting machine préparé tablets. Examples of adjuvants or diluents comprise: corn starch, potato starch, talcum, magnésium stéarate, gelatin, lactose, gums, and the like. Any other adjuvants or additives usually used for such purposes such as colorings, flavorings, preservatives etc. may be used provided that they are compatible with the active ingrédients.
TREATMENT OF DISORDERS
As mentioned above, the compounds of formula (I) are PDE1 enzyme inhibitors and as such are useful to treat associated neurological and psychiatrie disorders.
The invention thus provides a compound of formula (I) or a pharmaceutically acceptable acid addition sait thereof, as well as a pharmaceutical composition containing such a compound, for use in the treatment of another brain disease which could be a neurodegenerative disorder or a psychiatrie disorder. In a preferred embodiment the neurodegenerative disorder is selected from the group consisting of Alzheimer's Disease, Parkinson's Disease and Huntington's Disease. In another preferred embodiment the psychiatrie disorder is selected from the group consisting of Attention Déficit hyperactivity Disorder (ADHD), dépréssion, anxiety, narcolepsy, cognitive impairment and cognitive impairment associated with schizophrenia (CIAS). Other brain diseases could be e.g. restless leg syndrome.
The présent invention provides a method of treating a mammal, including a human, suffering from a neurodegenerative disorder selected from the group consisting of Alzheimer's Disease, Parkinson's Disease and Huntington's Disease, which method comprises administering to the subject a therapeutically effective amount of a compound of formula (I).
This invention further provides a method of treating a neurodegenerative disorder in a mammal, including a human, which method comprises administering to said mammal an amount of a compound of formula (I) effective in inhibiting PDE1.
This invention also provides a method of treating a subject suffering from a psychiatrie disorder, which method comprises administering to the subject a therapeutically effective amount of a compound of formula (I). Examples of psychiatrie disorders that can be treated according to the présent invention include Attention Déficit hyperactivity Disorder (ADHD), dépréssion, anxiety, narcolepsy, cognitive impairment and cognitive impairment associated with schizophrenia (CIAS).
This invention also provides a method of treating a subject suffering from another brain disorder such as restless leg syndrome.
Further, the invention is directed to the use of a compound of formula (I) in the manufacture of a médicament for the treatment of a neurodegenerative disorder, such as Alzheimer's Disease, Parkinsoris Disease and Huntington’s Disease or for the treatment of a psychiatrie disorder such as Attention Déficit hyperactivity Disorder (ADHD), dépréssion, anxiety, narcolepsy, cognitive impairment and cognitive impairment associated with schizophrenia (CIAS).
Further, the invention is directed to the use of a compound of formula (I) in the manufacture of a médicament for the treatment of another brain disease, such as restless leg syndrome
The invention is also directed to a compound of formula (I) for use as a medicine. In a spécifie embodiment the compound of formula (I) for use in the treatment of a neurodegenerative disorder, such as Alzheimer's Disease, Parkinsoris Disease and Huntington's Disease or for the treatment of a psychiatrie disorder such as Attention Déficit hyperactivity Disorder (ADHD), dépréssion, anxiety, narcolepsy cognitive impairment and cognitive impairment associated with schizophrenia (CIAS) or for the treatment of another brain disease like restless leg syndrome.
Ail references, including publications, patent applications and patents, cited herein are hereby incorporated by reference in their entirety and to the same extent as if each reference were individually and specifîcally indicated to be incorporated by reference and were set forth in its entirety (to the maximum extent permitted by law).
Headings and sub-headings are used herein for convenience only, and should not be construed as limiting the invention in any way.
The use of any and ail examples, or exemplary language (including “for instance, “for example”, “e.g , and “as such”) in the présent spécification is intended merely to better illuminate the invention, and does not pose a limitation on the scope of invention unless otherwise indicated.
The citation and incorporation of patent documents herein is done for convenience only, and does not reflect any view of the validity, patentability and/or enforceability of such patent documents.
The présent invention includes ail modifications and équivalents of the subject-matter recited in the daims appended hereto, as permitted by applicable law.
COMPOUNDS OF THE INVENTION
Table 1: Compounds of the invention
Example | Name | PDE1A, ICSÛ (nM) | PDE1B, ICjo (nM) | PDE1C, IC50 (nM) | % inhibition of PDE9 at 10 microM |
1 | 7-(3-Fluorobenzyl)-3propylimidazo[1,5-a]pyrazin8(7H)-one | 801 | 790 | 300 | -12 |
2 | 6-Benzyl-7-(3-fluorobenzyl)-3(tetrahydro-2/-/-pyran-4yl)imidazo[1,5-a]pyrazin-8(7H)one | 51 | 14 | 11 | -14 |
3 | 6-Benzyl-7-(cyclohexylmethyl)3-(tetrahydro-2H-pyran-4yl)imidazo[1,5-a]pyrazin-8(7H)one | 8 | 12 | 6 | -6 |
4 | 7-(Cyclohexylmethyl)-6-methyl3-(tetrahydro-2H-pyran-4yl)imidazo[1,5-a]pyrazin-8(7H)one | 11 | 25 | 7 | -5 |
5 | 7-(3-Fluorobenzyl)-6-methyl-3(tetrahydro-2H-pyran-4y|)imidazo[1,5-a]pyrazin-8(7H)one | 108 | 120 | 14 | 18 |
6 | 3-Cyclopropyl-7-(3fluorobenzyl)imidazo[1,5a]pyrazin-8(7H)-one | 68% (at 2 pM) | 81%(at2 pM) | 290 | 25 |
7 | 7-(Cyclopentylmethyl)-3cyctopropylimidazo[1,5a]pyrazin-8(7H)-one | 60% (at 2 pM) | 85% (at 2 pM) | 230 | 1 |
8 | 7-(Cyclohexylmethyl)-3cyclopropylimidazo[1,5a]pyrazin-8(7/-/)-one | 252 | 67 | 100 | 9 |
9 | 7-(3-F!uorobenzyl)-3(tetrahydro-2/-/-pyran-4yl)imidazo[1,5-a]pyrazi n-8(7H)one | 68% (at 2 pM) | 90% (at 2 pM) | 170 | 2 |
10 | 7-(Cyclopentylmethyl)-3(tetrahydro-2H-pyran-4y[)imidazo[1,5-a]pyrazin-8(7H)one | 73% (at 2 pM) | 88% (at 2 pM) | 79 | 8 |
11 | 7-(Cyclohexylmethyl)-3- (tetrahydro-2H-pyran-4yl)imidazo[1,5-a]pyrazin-8(7/-/)one | 113 | 72 | 43 | 18 |
25 | 6-Methyl-7-(3-methylbenzyl)-3(tetrahydro-2H-pyran-4yl)imidazo[1,5-a]pyrazin-8(7/7)one | 63 | 57 | 9 | -42 |
26 | 7-(3-fluorobenzyl)-6-methyl-3-(4methyltetrahydro-2H-pyran~4yl)imidazo[1,5-a]pyrazin-8(7/7)one | 234 | 218 | 47 | -2 |
27 | 4-(7-(3-fluorobenzyl)-6-methyl-8oxo-7,8-dihydroimidazo[1,5a]pyrazin-3-yl)tetrahydro-2Hpyran-4-carbonitrile | 603 | 699 | 103 | 5 |
28 | 7-(3-fluorobenzyl )-3-(4methoxytetrahydro-2/-/-pyran-4yl)-6-methylimidazo[1,5a]pyrazin-8(7/7)-one | 663 | 737 | 72 | 13 |
29 | 7-(3-fluorobenzyl)-3-(4fluorotetrahydro-2H-pyran-4-yl)6-methylimidazo[1,5-a]pyrazin8(7/-/)-one | 493 | 249 | 50 | 16 |
30, isomer 1 | 7-(3-fluorobenzyl)-6-methyl-3(tetrahydro-2H-pyran-2yl)imidazo[ 1,5-a]pyrazin-8(7/7)one, stereoisomer 1 | 20% (at 1 pM) | 615 | 225 | -11 |
30, isomer 2 | 7-{3-fluorobenzyl)-6-methyl-3(tetrahydro-2H-pyran-2yl)imidazo[1,5-a]pyrazin-8(7/-/)one, stereoisomer 2 | 27% (at 1 μΜ) | 40% (at 1 μΜ) | 215 | 28 |
31, isomer 1 | 7-(3-fluorobenzyl)-6-methyl-3(tetrahydrofuran-3yl)imidazo[1,5-a]pyrazin-8(7H)one, stereoisomer 1 | 337 | 106 | 27 | -1 |
31, isomer 2 | 7-(3-fluorobenzyl)-6-methyl-3(tetrahydrofuran-3yl)imidazo[1,5-a]pyrazin-8(7H)one, stereoisomer 2 | 347 | 138 | 31 | 5 |
32, isomer 1 | 7-(3-fluorobenzyl)-6-methyl-3-(3methyltetrahydrofuran-3yl)imidazo[1,5-a]pyrazin-8(7/-/)one, stereoisomer 1 | 257 | 122 | 22 | -1 |
32, isomer 2 | 7-(3-fluorobenzyl)-6-methyl-3-(3methyltetrahydrofuran-3yl)imidazo[1,5-a]pyrazin-8(7/-/)one, stereoisomer 2 | 401 | 170 | 40 | 16 |
33 | 7-(3-fluorobenzyl)-6-methyl-3-(1methylcyclopropyi)imidazo[1,5a]pyrazin-8(7/-/)-one | 94 | 52 | 7 | -2 |
34 | 3-(2,2-difluorocyclopropyl)-7-(3fluorobenzyl)-6methyiîmidazo[1,5-a]pyrazin8(7H)-one | 331 | 359 | 93 | 0 |
35, isomer 1 | 7-(3-fluorobenzyi)-6-methyl-3-(2methylcyclopropyl)imidazo[1,5a]pyrazin-8(7/7)-one, stereoisomer 1 | 193 | 75 | 19 | -11 |
35, isomer 2 | 7-(3-fluorobenzyl)-6-methyl-3-(2methylcyclopropy[)imidazo[1,5a]pyrazin-8(7H)-one, stereoisomer 2 | 364 | 166 | 41 | 15 |
35, isomer 3 | 7-(3-fluorobenzyl)-6-methy 1-3-(2metfiylcyclopropyl)tmidazo[1,5a]pyrazin-8(7H)-one, stereoisomer 3 | 82 | 18 | 8 | 0 |
35, isomer 4 | 7-(3-fluorobenzyl)-6-methyl-3-(2rnethytcyclopropyl)imidazo[1,5a]pyrazin-8(7H)-one, stereoisomer 4 | 43% (at 1 pM) | 360 | 85 | 5 |
36, isomer 1 | 7-(3-fluorobenzyl)-6-methyl-3-(2meth y I tet ra h y d rofu ra n -3yl)imtdazo[1,5-a]pyrazin-8(7H)one, stereoisomer 1 | 152 | 59 | 15 | 3 |
36, isomer 2 | 7-(3-fluorobenzyl)-6-methyl-3-(2methyltetrahydrofuran-3yl)imidazo[1,5-a]pyrazin-8(7H)one, stereoisomer 2 | 282 | 107 | 38 | 11 |
36, isomer 3 | 7-(3-fluorobenzy[)-6-methyl-3-(2methy Itetra hyd rofu ran-3yl )im idazo[ 1,5-a]pyrazin-8(7H)one, stereoisomer 3 | 77 | 21 | 7 | -10 |
36, isomer 4 | 7-(3-fluorobenzyl)-6-methyl-3-(2methyltetrahydrofuran-3yl)imidazo[1,5-a]pyrazin-8(7/-/)one, stereoisomer 4 | 51 | 520 | 40% (at 1 μΜ) | 11 |
37, isomer 1 | 7-(3-fluorobenzyl)-3-(C/S-2fluorocyclopropyl)-6methylimidazo[1,5-a]pyrazin8(7/7)-one, stereoisomer 1 | 1140 | 1180 | 345 | -2 |
37. isomer 2 | 7-(3-fluorobenzyl)-3-(c/s-2fluorocyclopropyl)-6methylimidazo[1,5-a]pyrazin8(7H)-one, stereoisomer 2 | 149 | 164 | 55 | 13 |
38, isomer 1 | 7-(3-fiuorobenzyl)-3-(frans-2- fluorocyclopropyl)-6- methylimidazo[1,5-a]pyrazin- 8(7H)-one, stereoisomer 1 | 582 | 601 | 118 | -1 |
38, isomer 2 | 7-(3-fluorobenzyl)-3-(frans-2fluorocyclopropyl)-6methylimidazo[1,5-a]pyrazin8(7H)-one, stereoisomer 2 | 667 | 667 | 153 | 2 |
39 | 7-(4-cyc!opropoxybenzyl)-6methyl-3-(tetrahydro-2/7-pyran4-yl)imidazo[1,5-a]pyrazin8(7H)-one | 413 | 118 | 364 | 23 |
40 | 7-(4-(difluoromethoxy)benzyl)-6methyl-3-(tetrahydro-2H-pyran4-yl)tmtdazo[1,5-a]pyrazin8(7H)-one | 73 | 27 | 52 | -25 |
41 | 6-methyl-3-(tetrahydro-2/-L pyran-4-yl)-7-(4(trifluoromethoxy)benzyl)imidazo [1,5-a]pyrazin-8(7H)-one | 27 | 18 | 52 | -22 |
42 | 7-(4- (cyclopropylmethoxy)benzyl)-6- methyl-3-(tetrahydro-2H-pyran- 4-yl)imidazo[1,5-a]pyrazin8(7H)-one | 50% (at 1 pM) | 155 | 55% (at 1 pM) | 15 |
43 | 7-benzyl-6-ethyl-3-(tetrahydro- 2H-pyran-4-yl)imidazo[1,5a]pyrazin-8(7 H)-one | 105 | 32 | 9 | 6 |
44 | 6-ethyl-7-(4-methoxybenzyl)-3(tetrahydro-2H-pyran-4yl)imidazo[1,5-a]pyrazin-8(7H)one | 40 | 5 | 16 | 18 |
45 | 3-((6-methyl-8-oxo-3(tetra h y d ro-2H-py ra n~4yl)imidazo[1,5-a]pyrazin-7(8H)yl)methyl)benzonitrile | 64 (at 2 pM) | 54% (at 1 pM) | 149 | 6 |
46 | 4-((6-methyl-8-oxo-3(tetrahydro-2H-pyran-4y I) imidazoî 1,5-a]pyrazin-7(8H)yl)methyl)benzonitrile | 809 | 58% (at 1 pM) | 9% (at 1 pM) | 14 |
47 | A/-(4-((6-methyl-8-oxo-3(tetrahydro-2H-pyran-4yl)imidazo[1,5-a]pyrazin-7(8H)yl)methyi)pheny[)acetamide | 0% (at 1 pM) | 388 | 10% (at 1 pM) | 10 |
48 | 7-(4-chloro-3-methoxybenzyf)-6methyl-3-(tetrahydro-2H-pyran4-yl)imidazo[1,5-a]pyrazin8(7H)-one | - | 54% (at 1 pM) | 34% (at 1 pM) | 10 |
49 | 7-(2-ethyibenzyl)-6-methyl-3(tetrahydro-2/7-pyran-4yl)imidazo[1,5-a]pyrazin-8(7/-/)one | 44 (at 2 pM) | 60% (at 1 pM) | 173 | 1 |
50 | 7-(benzo[d][1,3]dioxol-5ylmethy1)-6-methyl-3(tetrahydro-2H-pyran-4yl)imidazo[1,5-a]pyrazin-8(7H)one | 50 | 16 | 38 | 12 |
51 | 7-(3-chloro-4-methoxybenzyl)-6methyl-3-(tetrahydro-2H-pyran4-yl)imidazo[1,5-a]pyrazin8(7H)-one | 199 | 36 | 46 | 1 |
52 | 7-(4-aminobenzyl)-6-methyî-3(tetrahydro-2H-pyran-4yl)imidazoÎl,5-a]pyrazin-8(7H)one | 0% (at 1 pM) | 388 | 10% (at 1 pM) | -3 |
53 | 7-(4-hydroxybenzyl)-6-methy!-3(tetrahydro-2H-pyran-4yl)imidazo[1,5-a]pyrazin-8(7H)one | 401 | 35 | 84 | -41 |
54 | 6-ethyl-7-(3-fluorobenzyl)-3(tetrahydro-2H-pyran-4yl)imidazo[1,5-a]pyrazin-8(7H)one | 62 | 53 | 12 | 23 |
55, isomer 1 | 7-(4-methoxybenzyl)-6-methyl-3(2-methyltetrahydrofuran-3yl)imidazo[1,5-a]pyrazin-8(7H)one, stereoisomer 1 | 20 | 10 | 17 | 18 |
55, isomer 2 | 7-(4-methoxybenzyl)-6-methy!-3(2-methyltetrahydrofuran-3yl)imidazo[1,5-a]pyrazin-8(7H)one, stereoisomer 2 | 86 | 64 | 51 | -13 |
55, isomer 3 | 7-(4-methoxybenzyl)-6-methyl-3(2-methyltetrahydrofuran-3yl)imidazo[1,5-a]pyrazin-8(7H)one, stereoisomer 3 | 13 | 3 | 8 | 27 |
55, isomer 4 | 7-(4-methoxybenzyl)-6-methyl-3(2-methyltetrahydrofuran-3y[)imidazo[1,5-a]pyrazin-8(7H)one, stereoisomer 4 | 137 | 208 | 131 | 1 |
56 | 7-(4-methoxybenzyl)-6-methyl-3propylimidazo[1,5-a]pyrazin8(7H)-one | 65 | 21 | 43 | 7 |
57 | 7-( (6-m ethoxy py rid i n-3yl)methyl)-6-methyl-3(tetrahydro-2/7-pyran-4yl)imidazo[1,5-a]pyrazin-8(7/7)one | 45 | 26 | 84 | -5 |
58 | 6,7-dimethyl-3-(tetrahydro-2Hpyran-4-yl)imidazo[1,5a]pyrazin-8(7H)-one | 58% (at 10 pM) | 1767 | 44% (at 10 μΜ) | 36 |
59 | 7-ethyl-6-methyl-3-(tetrahydro- 2H-pyran-4-yi)imidazo[1,5a]pyrazin-8(7H)-one | 2333 | 496 | 1737 | -13 |
60 | 6-methyl-7-propyl-3-(tetrahydro- 2H-pyran-4-yi)imidazo[1,5a]pyrazin-8(7H)-one | 810 | 221 | 423 | -13 |
61 | 7-isopropyl-6-methyl-3- (tetrahydro-2H-pyran-4yl)imidazo[1,5-a]pyrazin-8(7H)one | 4% (at 10 pM) | 50% (at 10 μΜ) | 47% (at 10 μΜ) | 4 |
62 | 7-isopentyl-6-methyl-3- (tetrahydro-2H-pyran-4yi)imidazoÎl,5-a]pyrazin-8(7H)- one | 1078 | 558 | 93 | 7 |
63 | 7-(cyclopentylmethyl)-6-methyl3-(tetrahydro-2H-pyran-4yl)imidazo[1,5-a]pyrazin-8(7H)one | 183 | 82 | 17 | -3 |
64 | 2-((6-methyl-8-oxo-3- ( tetrah y d ro-2 H-pyran-4yl)imidazo[1,5-a]pyrazin-7(8H)y!)methy[)benzonitrile | 624 | 528 | 103 | 11 |
65 | 7-(cycloheptylmethyl)-6-methyl3-(tetrahydro-2H-pyran-4yl)imidazo[1,5-a]pyrazin-8(7/7)one | 10 | 6 | 5 | 11 |
66. trans | 6-methyl-7-(((trans)-4methylcyclohexyl)methyl)-3(tetrahydro-2/7-pyran-4yl)imidazo[1,5-a]pyrazin-8(7H)one | 35 | 11 | 46 | -2 |
66. cis | 6-methyl-7-(((cis)-4methylcyclohexy[)methyl)-3(tetrahydro-2H-pyran-4yl)imtdazo[1,5-a]pyrazin-8(7H)one | 7 | 6 | 4 | -3 |
67 | 7-(((CÎS)-4methoxycyclohexyl)methyl)-6methyl-3-(tetrahydro-2H-pyran4-yl)imidazo[1,5-a]pyrazin8(7H)-one | 234 | 87 | 307 | 10 |
68 | 7-(((trans)-4methoxycyclohexyl)methyl)-6methyl-3-(tetrahydro-2H-pyran4-yl)îmidazo[1,5-a]pyrazin8(7H)-one | 323 | 127 | 1859 | 5 |
69 | 7-(4-methoxybenzyl)-6-methyl-3- (3-methyltetrahydro-2H-pyran-4yl)imidazo[1,5-a]pyrazin-8(7H)one | 13 | 8 | 24 | 2 |
70 | 7-(4-methoxybenzyl)-6-methyl-3((1R,2R,4S)-2-methyl-7oxabicyclo[2.2.1]heptan-2yl)imidazo[1,5-a]pyrazin-8(7/-/)one | 29 | 17 | 28 | -11 |
71 | (S)-7-(4-methoxybenzyl)-6methyl-3-(1phenylethyl)imidazo[1,5a]pyrazin-8(7H)-one | 211 | 238 | 538 | 13 |
72 | (R)-7-(4-methoxy benzyl)-6methyl-3-(1phenylethyl)imidazo[1,5a]pyrazin-8(7H)-one | 90 | 12 | 43 | 9 |
73 | 3-(1:4-dimethylpiperidin-4-yl)-7(4-methoxybenzyl)-6methylimidazo[1,5-a]pyrazin8(7H)-one | 1923 | 1446 | 2450 | nd |
74 | 3-(6-chloro-2,3-dihydro-1 Hinden-1-yl)-7-(4-methoxybenzyl)6-methylimidazo[1,5-a]pyrazin8(7/-/)-one | 5 | 2 | 3 | -19 |
75 | 7-(4-methoxybenzyl)-6-methyl-3(3-methy[-5-oxopyrrolidin-3yl)imidazo[1,5-a]pyrazin-8(7/7)one | 236 | 297 | 360 | 8 |
75 | 3-(1-methoxy-2-methylpropan-2yl)-7-(4-fnethoxybenzyl)-6methylimidazo[1,5-a]pyrazîn8(7/7)-one | 122 | 44 | 126 | -14 |
77 | 3-isopropyl-7-(4methoxybenzyl)-6methylimidazo[1,5-ajpyrazin8(7/-/)-one | 13 | 7 | 20 | nd |
78 | 6-methyl-7-((2-methylthiazol-4yl)methyl)-3-(tetrahydro-2/7pyran-4-yl)imidazo[1,5a]pyraztn-8(7/7)-one | 1691 | 641 | 251 | 6 |
79 | 6-methyl-3-(tetrahydro-2/7pyran-4-yl)-7-(thiophen-3y!methyi)imidazo[1,5-a]pyrazin8(7/-/)-one | 228 | 112 | 15 | 14 |
80 | 6-methyl-3-(tetrahydro-2/7pyran-4-yl)-7-(thiazol-4ylmethyl)imidazo[1,5-a]pyrazin8(7/7)-one | 72%(at10pM) | 1310 | 496 | 18 |
81 | 7-((3,5-dimethylisoxazol-4yl)methyl)-6-methyl-3(tetrahydro-2/7-pyran-4yl)imidazo[1,5-a]pyrazin-8(7/7)one | 27% (at 10 μΜ) | 36% (at 10 μΜ) | 2305 | 36 |
82 | 6-methyl-7-((5-methylisoxazo[-3- yl)methyl)-3-(tetrahydro-2/7- pyran-4-yl)imidazo[1,5- a]pyrazin-8(7/7)-one | 67% (at 10 μΜ) | 1498 | 1034 | 7 |
83 | 6-methyl-7-((3-methylisoxazol-5yl)methyl)-3-(tetrahydro-2/7pyran-4-yl)imidazo[1,5a]pyrazin-8(7/7)-one | 4444 | 2289 | 1606 | -4 |
84 | 3-(2,6-dimethyltetrahydro-2/7pyran-4-yl)-7-(4methoxybenzyl)-6methylimidazo[1,5-a]pyrazin8(7H)-one | 627 | 103 | 337 | -5 |
85 | 7-(cyclohexylmethyl)-6-methyl-3propylimidazo[1,5-a]pyrazin8(7/7)-one | 120 | 32 | 32 | 7 |
86 | 3-(2-hydroxypropan-2-yl)-7-(4methoxybenzyl)-6methylimidazo[1,5-a]pyrazin8(7/7)-one | 193 | 118 | 214 | -11 |
87 | 3-(2-fl uoropropan-2-y 1)-7-(4methoxybenzyl)-6methylimidazo[1,5-a]pyrazin8(7/7)-one | 108 | 124 | 276 | 10 |
88 | 7-(4-methoxybenzyl)-6-methyl-3(7-oxoazepan-4-yl)imidazo(1,5a]pyrazin-8(7/7)-one | 484 | 308 | 548 | -32 |
89 | 7-(4-methoxybenzyl)-6-methyl-3(5-methyltetrahydrofuran-3yl)imidazo[1,5-a]pyrazin-8(7/7)one | 65% (at 10 μΜ) | 128 | 303 | 1 |
90 | 7-(4-methoxybenzyl)-6-methyl-3( 1 -(4-methylthiazol-2yl)ethyl)imidazo[1,5-a]pyrazin8(7/7) -one | 34 | 15 | 23 | 10 |
91 | 3-(7-(4-methoxybenzyl)-6methyl-8-oxo-7,8dihydroimidazo[1,5-a]pyrazin-3yl)-3-methy!pyrrolidine-1sulfonamide | 181 | 185 | 417 | 20 |
92 | 6-(cyclopentylmethyi)-7-(4methoxybenzyl)-3-(tetrahydro2/7-pyran-4-yl)imidazo[1,5a]pyrazin-8(7/7)-one | 71 | 11 | 79 | 57 |
93 | 3-(morpholino)-7-(4methoxybenzyl)-6methylimidazo[1,5-ajpyrazin8(7/-/)-one | 96 | 52 | 99 | 23 |
94 | 7-(4-methoxybenzyl)-6-methyl-3((tetrahydrofuran-3yl)amino)imidazo[1,5-a]pyrazin8(7/7)-one | 2516 | 465 | 1231 | -5 |
95 | (R)-7-(4-methoxybenzyl)-6methyl-3-(3methylmorpholino)imidazo[1,5a]pyrazin-8(7/7)-one | 258 | 162 | 218 | 9 |
96 | (S)-7-(4-methoxybenzyl)-6methyl-3-(3methylmorpholino)imidazo[1,5a]pyrazin-8(7/7)-one | 48 | 38 | 51 | nd |
97 | 7-(4-methoxybenzyl)-6-methyl-3(1,4-oxazepan-4-yl)imidazo[1,5a]pyrazin-8(7/7)-one | 202 | 82 | 128 | -8 |
98 | 3-(2,2-dimethylmorpholino)-7-(4methoxybenzy[)-6methylimidazo[1,5-a]pyrazîn8(7/7)-one | 287 | 102 | 135 | 4 |
99, isomer 1 | 7-(3-fluorobenzyl)-3-(hexahydro4/7-furo[3,2-b]pyrrol-4-yl)-6methyîimidazo[1,5-a]pyrazin8(7/7)-one, isomer 1 | 241 | 134 | 27 | 9 |
99, isomer 2 | 7-(3-fluorobenzyl)-3-(hexahydro4H-furo[3,2-b]pyrrol-4-yl)-6methylimidazo[1,5-a]pyrazin8(7H)-one, isomer 2 | 47% (at 10 μΜ) | 760 | 119 | 6 |
100, isomer 1 | 7-(3-fluorobenzyl)-6-methyl-3(tetrahydro-2H-pyran-3yl)imidazo[ 1,5-a]pyrazin-8(7/-/)one, stereoisomer 1 | 306 | 223 | 43 | 11 |
100, isomer 2 | 7-(3-fluorobenzyl)-6-methyl-3(tetrahydro-2H-pyran-3yl)imidazo[1,5-a]pyrazin-8(7H)one, stereoisomer 2 | 333 | 93 | 33 | -21 |
nd means “not determined
Table 1 lists the IC50 value for inhibition of PDE1 by the compounds of the invention. The ΙΟ50 value refers to the concentration (nM) of the compound required to reach 50% inhibition of the PDE1 enzyme at the specified substrate concentration.
For certain compounds, the inhibition of PDE is listed as % inhibition at a certain concentration.
For comparative purpose, the table also lists % inhibiton of PDE9 at 10 μΜ.
PDE1 and PDE9 assays are described in the Experimental Section.
EXPERIMENTAL SECTION
PREPARATION OF THE COMPOUNDS OF THE INVENTION
O
(I)
The compounds of formula (I) may be prepared by methods described below, together with 15 synthetic methods known in the art of organic chemistry, or modifications that are familiar to those of ordinary skill in the art. The starting materials used herein are available commercially or may be prepared by routine methods known in the art, such as those method described in standard reference books such as “Compendium of Organic Synthetic
Methods, Vol. Ι-ΧΙΓ (published with Wiley-lnterscience, ISSN: 1934-4783). Preferred methods include, but are not limited to, those described below.
The schemes are représentative of methods useful in synthesizing the compounds of the présent invention. They are not to constrain the scope of the invention in any way. Unless otherwise indicated, in the reaction schemes and discussion that follow, R,-R4 are as defined in claim 1.
General Methods:
Method 1:
n = 0,1 o
In brief, compounds of the invention can be prepared from the commercial available (3chioropyrazin-2-yl)methanamine dihydrochloride V (CAS. 867165-53-5). Reacting (3chloropyrazin-2-yl)methanamine dihydrochloride V with an acid dérivative exemplified by but not limited to an acid chloride under conditions appropriate for amide formation, using a base exemplified by but not limited to triethylamine and a solvent/solvent mixture such as dimethylformamide and dichloromethane yields amide IV. Intermediate III can be prepared from IV by treatment with phosphoryl chloride in a solvent such as dioxane. The 8chloroimidazo[1,5-a]pyrazine III is converted to imidazo[1,5-a]pyrazin-8(7/7)-one 11 under standard hydrolysis conditions exemplified by but not limited to hydrochloric acid in a solvent mixture such as water and 1,4-dioxane. Compound I is formed from imidazo[1,5-a]pyrazin8(7H)-one II by treatment with an alkylating reagent exemplified by but not limited to an alkyl bromide using a base exemplified but not limited to potassium carbonate in a solvent such as dimethylformamide,
Method 2:
In brief, compounds of the invention can be prepared from the commercial available 5amino-3-methoxypyrazine-2-carbonitrile X (CAS: 1137478-55-7). Reaction of 5-amino-3methoxypyrazine-2-carbonitrile X with di-tert-butyl bicarbonate and a catalyst exemplified by but not limited to /V,A/-dimethylpyridin-4-amine in a solvent such as dichloromethane gives pyrazine IX. Hydrogénation of IX with a catalyst exemplified but not limited to Raney Nickel under an atmosphère of hydrogen in a solvent such as methanol yields amine VIII. Compounds of formula VII can be prepared by employing compounds of formula VIII and a carboxylic acid using standard amide bond forming conditions exemplified but not limited to HATU (1-[Bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium 3-oxid hexafluorophosphate), a base, exemplified but not limited to triethylamine in a solvent such as dichloromethane. Boc protected compounds of formula VII can be deprotected to compounds of formula VI using standard de-protection conditions exemplified by but not limited to trifluoroacetic acid in a solvent such as dichloromethane. Treating compounds of formula VI with isoamyl nitrite, copper iodide and diiodomethane in a solvent such as tetrahydrofuran yields compounds of formula V. Compounds of formula V can be converted to imidazopyrazines of formula IV by treatment with phosphoryl chloride in a solvent such as 1,4-dioxane. Imidazopyrazines of formula III are prepared from IV using standard cross coupling reaction conditions exemplified by but not limited to a Suzuki-Miyaura crosscoupling reaction. Such conditions for the cross coupling reaction are exemplified by but not limited to using; a boronic acid ester, potassium carbonate as the base, a mixture of 1,4dioxane and water as the solvent and [1,T-bis(diphenylphosphino) ferrocene]dichloropalladium(ll) (Pd(dppf)CI2) as the catalyst. lmidazo[1,5-a]pyrazin-8(7/-/)ones of formula II are prepared by treating compounds of formula III with an acid exemplified but not limited to hydrochloric acid in a mixture of solvents such as water and methanol. Imidazo[1,5-a]pyrazin-8(7H)-ones of formula I are prepared by alkylation of II with an alkylating reagent exemplified by but not limited to alkylbromide using a base exemplified by but not limited to potassium carbonate in a solvent such as dimethylformamide.
Method 3:
R4 = H
In brief, compounds of the invention can be prepared from the commercial available methyl 1H-imidazole-5-carboxylate VI (CAS: 17325-26-7). Reaction of methyl 1 H-imidazole-5carboxylate VI with an α-halogenated ketone exemplified but not limited to an achloroketone, under the influence of a base exemplified but not limited to potassium carbonate in a solvent such as acetone yields the imidazole V. Treating imidazole V with a brominating reagent exemplified but not limited to A/-bromosuccinimide (NBS) in the presence of a radical initiator exemplified by but not limited to azobisisobutyronitrile (Al B N) gives imidazole IV. Compounds of the formula III are formed by treatment imidazole IV with ammonium acetate in a solvent such as 1,4-dioxane. Compounds ofthe formula II can be prepared from intermediate III using standard cross-coupling reaction conditions exemplified by but not limited to a Suzuki-Miyaura cross-coupling reaction. Such conditions for the crosscoupling reaction are exemplified by but not limited to using; a boronic acid ester, potassium carbonate as the base, a mixture of 1,4-dioxane and water as the solvent and Pd(dppf)CI2 as the catalyst. In some examples Ρη contains an unsaturated carbon-carbon bond which can be reduced by hydrogénation under conditions known to the person skilled in the art. lmidazo[1,5-a]pyrazin-8(7/-0-ones of formula I are prepared by alkylation of 11 with an alkylating reagent exemplified by but not limited to alkylbromide using a base exemplified by but not limited to potassium carbonate in a solvent such as dimethylformamide.
Method 4:
o
n = 0,1
In brief, compounds of the invention can be prepared from the commercial available 2chloro-6-methylpyrazine X (CAS: 38557-71-0). Reacting 2-chloro-6-methylpyrazine X with Sodium methoxide in methanol yields pyrazine IX. /V-oxide VIII can be prepared from IX, by treatment with an oxidant, not limited to sodium metaborate and hydrogen peroxide, in a solvent such as acetic acid. Reacting VIII with a cyanide source, such as trimethyIsilyl cyanide and zinc(ll)bromide, using a base exemplified by but not limited to triethylamine and a solvent/solvent mixture such as acetonitrile yields cyanide VII. Réduction of VII, not limited to Raney nickel and hydrogen, in the presence of Boc-anhydride, produces carbamate VI. Amine V can be liberated by use of trifluoro acetic acid, but not limited to, from VI. Reacting amine V with an acid dérivative exemplified by but not limited to an acid chloride under conditions appropriate for amide formation, using a base exemplified by but not limited to triethylamine and a solvent/solvent mixture such as dimethylformamide and dichloromethane yields amide IV. Intermediate III can be prepared from IV by treatment with phosphoryl chloride in a solvent such as dioxane. The 8-chloroimidazo[1,5-a]pyrazine III is converted to imidazo[1,5-a]pyrazin-8(7/-/)-one II under standard hydrolysis conditions exemplified by but not limited to hydrochloric acid in a solvent mixture such as water and 1,4-dioxane. Compound I is formed from imidazo[1,5-a]pyrazin-8(7/-/)-one II by treatment with an alkylating reagent exemplified by but not limited to an alkyl bromide using a base exemplified but not limited to potassium carbonate in a solvent such as dimethylformamide.
Analytical Methods
Analytical LC-MS data were obtained using the methods identified below.
Method 1: An Agilent 1200 LCMS system with ELS detectorwas used. Column: XBridge ShieldRP18, 5 pm, 50x2.1 mm; Column température: 40 °C; Solvent system: A = water/NH3*H2O (99.95:0.05) and B = acetonitrile; Method: Linear gradient elution with A:B = 99:1 to 0:100 in 3.4 minutes and with a flow rate of 0.8 mUmin.
Method 2: A Shimadzu 20 MS instrument equipped with atmospheric pressure photo ionisation ion source and a Shimadzu LC-20AB system was used. Column: MERCK, RP-18e 25-2mm; Column température: 50 °C; Solvent System: A = water/trifluoroacetic acid (99.9625.0375) and B = acetonitrile /trifluoroacetic acid (99.981:0.019); Method: A linear gradient elution A:B = 95:5 to A:B=5:95 in 0.7 minutes, then A:B=5:95 for 0.4 minutes, then with a linear gradient elution to A: B 95:5 for 0.4 minutes with a constant flow rate of 1.5 mL/min.
Method 3: An Agilent 1200 LCMS system with ELS detectorwas used. Column: Agilent TC-C18 5 pm; 2.1x50mm; Column température: 50 °C; Solvent system: A = water/trifluoroacetic acid (99.9:0.1) and B = acetonitrile /trifluoroacetic acid (99.95:0.05); Method: Linear gradient elution with A:B = 99:1 to 0:100 in 4.0 minutes and with a flow rate of 0.8 mL/min.
Method 4: An Agilent 1200 LCMS System with ELS detectorwas used. Column: Agilent TC-C18 5 pm; 2.1x50mm; Column température: 50 °C; Solvent system: A = water/trifluoroacetic acid (99.9:0.1) and B = acetonitrile /trifluoroacetic acid (99.95:0.05); Method: Linear gradient elution with A:B = 90:10 to 0:100 in 4.0 minutes and with a flow rate of 0.8 mL/min.
Method 5: A Waters Acquity UPLC-MS was used. Column: Acquity UPLC BEH C18 1.7pm; 2.1x50mm; Column température: 60 “C; Solvent system: A = water/trifluoroacetic acid (99.965:0.035) and B = acetonitrile /water/trifluoroacetic acid (94.965:5:0.035); Method: Linear gradient elution with A:B = 90:10 to 0:100 in 1.0 minutes and with a flow rate of 1.2 mL/minute.
Method 6: A Waters Acquity UPLC-MS was used. Column: Acquity UPLC BEH C18 1.7pm; 2.1x50mm; Column température: 60 CC; Solvent System: A = water/fomnic acid (99.9:0.1) and B = acetonitrile /water/fomnic acid (94.9:5:0.1); Method: Linear gradient elution with A:B = 90:10 to 0:100 in 1.0 minutes and with a flow rate of 1.2 mUminute.
Method 7: A Waters Acquity UPLC-MS was used. Column: Acquity UPLC HSS T3 C18 1,8pm; 2.1x50mm; Column température: 60 °C; Solvent System: A = water/trifluoroacetic acid (99.965:0.035) and B = acetonitrile /water/trifluoroacetic acid (94.965:5:0.035); Method: Linear gradient elution with A:B = 98:02 to 0:100 in 1.0 minutes and with a flow rate of 1.2 mL/min.
Method 8: An Agilent 1200 LCMS system with ELS detector was used. Phenomenex Luna-C18, 5pm: 2.0x50mm; Column température: 50 °C; Solvent System: A = water/trifluoroacetic acid (99.9:0.1) and B = acetonitrile /trifluoroacetic acid (99.95:0.05); Method: Linear gradient elution with A:B = 99:1 to 0:100 in 4.0 minutes and with a flow rate of 0.8 mL/min.
Method 9: An Agilent 1200 LCMS system with ELS detector was used. Column: Xtimate C18 2.1‘30mm,3um; 2.0x50mm; Column température: 50 °C; Solvent system: A = water/trifluoroacetic acid (99.9996:0.0004) and B = acetonitrile /trifluoroacetic acid (99.9998:0.0002); Method: Linear gradient elution with A:B = 100:0 to 70:30 in 3.0 minutes and with a flow rate of 0.8 mL/min.
Method 10: An Agilent 1200 LCMS system with ELS detector was used. Column: Xtimate C18 2.1*30mm,3um; 2.0x50mm; Column température: 50 °C; Solvent system: A = water/trifluoroacetic acid (99.9996:0.0004) and B - acetonitrile /trifluoroacetic acid (99.9998:0.0002); Method: Linear gradient elution with A:B = 100:0 to 40:60 in 1.5 minutes and with a flow rate of 1.2 mL/min.
Method 11 : An Agilent 1200 LCMS system with ELS detector was used. Column: Waters XBridge ShieldRP18,2.1*50mm,5pm; Column température: 40 °C; Solvent system: A = water/ammonia (99.95:0.05) and B = acetonitrile; Method: Linear gradient elution with A:B = 95:5 to 0:100 in 4.0 minutes and with a flow rate of 0.8 mL/min.
Method 12: An Agilent 1100 LCMS system with ELS detector was used. Column: YMC ODS-AQ 5 pm; 2.0x50mm; Column température: 50 °C; Solvent system: A = water/trifluoroacetic acid (99.9:0.1) and B = acetonitrile /trifluoroacetic acid (99.95:0.05); Method: Linear gradient elution with A:B = 99:1 to 5:95 in 3.5 minutes and with a flow rate of 0.8 mL/min.
Method 13: An Agilent 1200 LCMS system with ELS detector was used. Phenomenex LunaC18, 5pm; 2.0x50mm; Column température: 50 °C; Solvent system: A = water/trifluoroacetic acid (99.9:0.1) and B = acetonitrile /trifluoroacetic acid (99.95:0.05); Method: Linear gradient elution with A:B = 99:1 to 0:100 in 4.0 minutes and with a flow rate of 0.8 mL/min.
Method 14: An Agilent 1200 LCMS system with ELS detector was used. Column: Xtimate C18 2.1*30mm,3um; 2.0x50mm; Column température: 50 °C; Solvent system: A = water/trifluoroacetic acid (99.9996:0.0004) and B = acetonitrile / trifluoroacetic acid (99.9998:0.0002); Method: Linear gradient elution with A:B = 100:0 to 40:60 in 6.0 minutes and with a flow rate of 0.8 mL/min.
Method 15: An Agilent 1200 LCMS system with ELS detector was used. Column: MERCK, RP18e 25-2mm, Column température: 50 °C; Solvent system: A = water/trifluoroacetic acid (99.9996:0.0004) and B = acetonitrile /trifluoroacetic acid (99.9998:0.0002); Method: Linear gradient elution with A:B = 95:5 to 5:95 in 0.7 minutes and with a flow rate of 1.5 mL/min.
Method 16: An Agilent 1200 LCMS system with ELS detector was used. Column: Xtimate C18 2.1*30mm,3um: 2.0x50mm; Column température: 50 °C; Solvent system: A = water/trifluoroacetic acid (99.9996:0.0004) and B - acetonitrile /trifluoroacetic acid (99.9998:0.0002); Method: Linear gradient elution with A:B = 100:0 to 40:60 in 0.9 minutes and with a flow rate of 1.2 mL/min.
Method 17: An Agilent 1200 LCMS system with ELS detector was used. Phenomenex LunaC18, 5pm; 2.0x50mm; Column température: 50 °C; Solvent system: A = water/trifluoroacetic acid (99.9:0.1) and B = acetonitrile /trifluoroacetic acid (99.95:0.05); Method: Linear gradient elution with A:B - 90:10 to 0:100 in 4.0 minutes and with a flow rate of 0.8 mL/min.
Method 18: An Agilent 1200 LCMS system with ELS detector was used. Column: Waters XBridge ShieldRP18,2.1*50mm,5pm; Column température: 40 °C; Solvent system: A = water/ammonia (99.95:0.05) and B = acetonitrile; Method: Linear gradient elution with A:B = 85:15 to 0:100 in 3.4 minutes and with a flow rate of 0.8 mL/min.
Method 19: A Waters Acquity UPLC-MS was used. Column: Acquity UPLC BEH C18 1.7pm; 2.1x50mm; Column température: 60 °C; Solvent system: A = water/formic acid (99.9:0.1) and B = acetonitrile /water/formic acid (94.9:5:0.1 ); Method: Linear gradient elution with A:B = 98:2 to 0.1:99.9 in 1.0 minutes and with a flow rate of 1.2 mL/minute.
Preparative LC-MS-purification was performed on a PE Sciex API 150EX instrument with atmospheric pressure Chemical ionization. Column: 50 X 20 mm YMC ODS-A with 5 pm particle size; Solvent System: A - water/trifluoroacetic acid (99.965:0.035) and B = acetonitrile /water/trifluoroacetic acid (94.965:5:0.035); Method: Linear gradient elution with A:B = 80:20 to 0:100 in 7 minutes and with a flow rate of 22.7 mL/minute. Fraction collection was performed by split-fiow MS détection.
Preparative SFC was performed on a Thar 80 instrument. Exemplified conditions can be, but not limited to: Column AD 250 X 30mm with 20 pm particle size; Column température: 38 °C, Mobile phase: Supercritical CO2/ EtOH(0.2%NH3H2O) =45/55.
Intermediates:
N-((3-chïoropyrazin-2-yl)methyI)butyramide:
Cl O
To an ice-cold solution of (3-chloropyrazin-2-yl)methanamine (2.0 g, 14 mmol) in dichloromethane (50 mL) and dimethylformamide (10mL) was added triethylamine(4.5 g, 45 mmol), followed by butyryl chloride (2 0 g. 14 mmol). The reaction was allowed to warm to room température and stirred for 1 hour. The reaction mixture was quenched with water and extracted with dichloromethane (2*250 mL). The combined organic phases were washed with brine, dried over Na2SO4 and concentrated in vacuo to afford /V-((3-chloropyrazin-2yl)methyl)butyramide 2.4 g (81%).
8-Chloro-3-propylimidazo[1,5-a]pyrazine:
To a solution of /\/-((3-chloropyrazin-2-yl)methyl)butyramide (2.4 g, 11 mmol) in 1,4-dioxane (20 mL) was added POCI3 (3.44 g, 22.5 mmol). The mixture was stirred at 100°C for 2 hrs and then cooled on an ice-bath. Saturated. aq. NaHCO3was added carefully and the mixture was extracted with dichloromethane (2*50 mL), The combined organic phases were washed with brine, dried over Na2SO4 and concentrated in vacuo to give 8-chloro-3propylimidazo[1,5-a]pyrazine 2 g (63%).
3-Propylimidazo[1,5-a]pyrazin-8(7H)-one:
A solution of 3-propylimidazo[1,5-a]pyrazin-8(7/-/)-one (100 mg, 0.51 mmol) in a mixture of 1,4-dioxane (10 mL) and H2O (4mL) was stirred at 100°C for 2 hours. The reaction mixture was concentrated in vacuo and the residue was diluted with dichloromethane (50 mL), washed with NaHCO3(aq), then brine, dried over Na2SO4 and concentrated in vacuo to give 3-propylimidazo[1,5-a]pyrazin-8(7H)-one 50 mg (55%).
Methyl 1-(2-oxopropyl)-1H-imidazole-5-carboxylate:
A mixture of methyl 1/-/-imidazole-5-carboxylate (20 g, 0.16 mol), 1-chloropropan-2-one (22 g, 0.24 mol), and potassium carbonate (44 g, 0.32 mol) in acetone (400 mL) was stirred at 30°C for 12 hours. The reaction mixture was concentrated in vacuo, the residue was diluted with ethyl acetate (200 mL) and washed with H2O (3*50 mL). The organic layer was dried over Na2SO4 and concentrated in vacuo. The residue was purified by flash chromatography using a gradient of petroleum ether and ethyl acetate to give methyl 1-(2-oxopropyl)-1/-/imidazole-5-carboxylate 10 g (35%).
Methyl 2-bromo-1-(2-oxopropyl)-1 H-imidazole-5-carboxylate:
A mixture of methyl 1-(2-oxopropyl)-1/-/-imidazole-5-carboxylate (10 g, 55 mmol), Nbromosuccinimide (12.7 g, 71.4 mmol) and azobisisobutyronitrile (1.8 g, 11 mmol) in chloroform (100 mL) was stirred at 50°C for 12 hours. The mixture was concentrated in vacuo. The residue was purified by flash chromatography using a gradient of petroleum ether and ethyl acetate to give methyl 2-bromo-1-(2-oxopropyl)-1/-/-imidazole-5-carboxylate 13 g (91%).
3-Bromo-6-methylimidazo[1,5-a]pyrazin-8(7H)-one:
ο
Br
A mixture of methyl 2-bromo-1-(2-oxopropyl)-1/7-imidazole-5-carboxylate (14 g, 50 mmol) and ammonium acetate (16.5 g, 215 mmol) in 1,4-dioxane (150 mL) was stirred at 60°C for 12 hours. The mixture was then stirred at 90°C for another 24 hours. The reaction mixture was concentrated in vacuo and the residue was diluted with ethyl acetate (600 mL) and washed with water (3*100 mL). The combined organic phases were dried with anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by flash chromatography using a gradient of petroleum ether and ethyl acetate to give 3-bromo-6methylimidazo[1,5-a]pyrazin-8(7/7)-one 4.8 g (39%).
3-(3,6-Dihydro-2M-pyran-4-yl)-6-methylimidazo[1,5-a]pyrazin-8(7H)-one:
A mixture of 3-bromo-6-methylimidazo[1,5-a]pyrazin-8(7H)-one (4.5 g, 20 mmol), 2-(3,6dihydro-2/-/-pyran-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (4.97 g, 23.7 mmol), Pd(dppf)CI2 (2.9 g, 3.95 mmol), potassium carbonate (5.5 g, 39 mmol) and H2O (10 mL) in 1,4-dioxane (40 mL) was stirred at 100°C for 12 hours. The mixture was filtred and the filtrate was concentrated in vacuo. The residue was purified by flash chromatography using a gradient of dichloromethane and methanol to give 3-(3,6-dihydro-2/7-pyran-4-yl)-6methylimidazo[1,5-a]pyrazin-8(7H)-one 4.0 g (88%).
6-Methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1I5-a]pyrazin-8(7H)-one:
o
A mixture of 3-(3,6-dihydro-2/7-pyran-4-yl)-6-methylimidazo[1,5-a]pyrazin-8(7H)-one (4.0 g, 17 mmol) and 10% Pd/C (300 mg) in tetrahydrofuran (15 mL) was stirred at 15° C for 7 hrs under an atmosphère of hydrogen. The reaction mixture was filtered and the filtrate was concentrated in vacuo to afford 6-methyl-3-(tetrahydro-2/7-pyran-4-yl)imidazo[1,5-a]pyrazin5 8(7H)-one 3.5 g (87%).
Tert-butyl (5-cyano-6-methoxypyrazin-2-yl)carbamate:
HN
EJ oc
CN
A solution of 5-amino-3-methoxypyrazine-2-carbonitrile (4.70 g, 31.3 mmol), di-tert-butyl dicarbonate (8.9 g, 41 mmol), A/,A/-dimethylpyridin-4-amine (38 mg, 0.31 mmol) in dichloromethane (150 mL) was stirred at 30°C for 12 hours. The reaction mixture was concentrated in vacuo. The residue was purified by flash chromatography using a gradient of petroleum ether and ethyl acetat to afford tert-butyl (5-cyano-6-methoxypyrazin-
2-yl)carbamate 9.0 g (80%).
Tert-butyl (5-(aminomethyl)-6-methoxypyrazin-2-yl)carbamate:
Boc
A mixture of tert-butyl (5-cyano-6-methoxypyrazin-2-yl)carbamate (9.0 g, 36 mmol), Raney Ni 40-60 mesh (5 g) and sat. NH3 in methanol (2 mL) in methanol (100 mL) was stirred at
30°C for 12 hrs under H2 (45 psi). The reaction was filtered and concentrated in vacuo to afford tert-butyl (5-(aminomethyl)-6-methoxypyrazin-2-yl)carbamate 10 g, sufficiently pure for the next step.
Tert-butyl (6-methoxy-5-((tetrahydro-2H-pyran-4-carboxamido)methyl)pyrazin-225 yl)carbamate:
A solution of tert-butyl (5-(aminomethyl)-6-methoxypyrazin-2-yl)carbamate (10.0 g, 31.5 mmol), tetrahydro-2H-pyran-4-carboxylic acid (4.50 g, 34.6 mmol), triethylamine (6.37 g, 62 9 mmol) and 1-[bis(dimethylamino)methylene]-1H-1 T2,3-triazolo[4,5-b]pyridinium 3-oxide hexafluoro phosphate (13.2 g, 34.6 mmol) in dichloromethane (120 mL) was stirred at 30°C for 12 hours. The reaction mixture was concentrated in vacuo and the residue was purified by flash chromatography using a gradient of petroleum ether and ethyl acetate to afford tertbutyl (6-methoxy-5-((tetrahydro-2/-Apyran-4-carboxamido)methyl)pyrazin-2-yl)carbamate 8 g (69.4%).
/V-((5-Amino-3-methoxypyrazin-2-yI)methyl)tetrahydro-2H-pyran-4-carboxamîde:
'o o
Boc
Ό O
A solution of tert-butyî (6-methoxy-5-((tetrahydro-2/7-pyran-4-carboxamido)methyl)pyrazin-2yl)carbamate (8 g, 21.8 mmol) and trifluoroacetic acid (40 mL) in dichloromethane(40 mL) was stirred at 30°C for 12 hours. The reaction mixture was concentrated in vacuo. The residue was diluted with dichloromethane (100 mL), and washed with NaHCO3 until pH=8. The organic layer was washed with water (3*20 mL), dried and concentrated in vacuo. The residue was purified by flash chromatography using a gradient of petroleum ether and ethyl acetate to yield A/-((5-amino-3-methoxypyrazin-2-yl)methyl)tetrahydro-2/7-pyran-4carboxamide 4 g (65.4%).
N-((54odo-3-methoxypyrazin-2-yl)methyl)tetrahydro-2H-pyran-4-carboxamide:
'Ό O
'O O
A solution of /\/-((5-amino-3-methoxypyrazin-2-yl)methyl)tetrahydro-2H-pyran-4-carboxamide (2.40 g, 9.01 mmol), copper(l)iodide (1.72 g, 9.01 mmol), isoamyl nitrite (1.58 g, 13.5 mmol) and diiodomethane (2.41 g, 9.01 mmol) in tetrahydrofuran (50 mL) was stirred at
75°C for 6 hours. The mixture was filtered and concentrated in vacuo. The residue was purified by flash chromatography using a gradient of petroleum ether and ethyl acetate to afford A/-((5-iodo-3-methoxypyrazin-2-yl)methyl)tetrahydro-2/-/-pyran-4-carboxamide 2.20 g (64.7%).
6-lodo-8-methoxy-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazine:
To a solution of A/-((5-iodo-3-methoxypyrazin-2-yl)methyl)tetrahydro-2/-/-pyran-4carboxamide (2 g, 5.30 mmol) in 1,4-dioxane (60 mL) was added phosphoryl chloride (8.13 g, 53.0 mmol) at 0°C. The reaction was stirred at 85°C for 12 hours. The mixture was concentrated in vacuo. The residue was diluted with dichloromethane (100 mL) and icewater (60 mL), followed by saturated aqueous NaHCO3 (30 mL). The organic phase was separated and the water phase was extracted with dichloromethane (3χ20 mL). The combined organic phases were combined, dried and concentrated in vacuo. The residue was purified by flash chromatography using a gradient of petroleum ether and ethyl acetate to yield 6-iodo-8-methoxy-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazine 500 mg (23.6%).
6-Benzyl-8-methoxy-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazine:
A mixture of 6-iodo-8-methoxy-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazine (500 mg, 1,39 mmol), 2-benzyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (911 mg, 4.18 mmol), Pd(dppf)CI2 (51 mg, 0.07 mmol), K2CO3 (577 mg, 4.18 mmol) and H2O (3 mL) in 1,4-dioxane (15 mL) was stirred at 80°C for 12 hrs under an atmosphère of N2. It was then filtred and the filtrate was concentrated in vacuo. The residue was purified by flash chromatography using a gradient of petroleum ether and ethyl acetate to yield 6-benzyl-8-methoxy-3-(tetrahydro-2Hpyran-4-yl)imidazo[1,5-a]pyrazine 260 mg (52%).
6-Benzyl·3-(tetΓahydΓO-2H-pyran-4-yl)imidazo[1l5-a]pyrazin-8(7H)-one:
A solution of 6-benzyl-8-methoxy-3-(tetrahydro-2/7-pyran-4-yl)imidazo[1,5-a]pyrazine (320 mg, 0.990 mmol) and 2 M aq. HCl (8 mL) in methanol (20 mL) was stirred at 60“C for 12 hours. The solution was concentrated in vacuo. The residue was purified by flash chromatography using a gradient of petroleum ether and ethyl acetate to yield 6-benzyl-3(tetrahydro-2H-pyran-4-yl)tmidazo[1,5-a]pyrazin-8(7/7)-one 230 mg (68%).
N-((3-chloropyrazin-2-yl)methyl)tetrahydro-2H-pyran-4-carboxamide:
Cl O
To a solution of (3-chloropyrazin-2-yl)methanamine dihydrochloride (3.8 g, 18 mmol) in anhydrous DMF (20 mL) was added triethylamine (5.7g, 56 mmol). The mixture was cooled to 0°C, tetrahydro-2H-pyran-4-carbonyl chloride (2.9 g, 19 mmol) was added dropwise. The mixture was stirred at 0°C for 0.5 hours. The reaction mixture was diluted with water (50 mL) and extracted with ethyl acetate (3*80 mL). The combined organic phases were washed with brine (50 mL), dried over Na2SO4 and concentrated in vacuo. The residue was purified by flash chromatography eluting with ethyl acetate to afford N-((3-chloropyrazin-2yl)methyl)tetrahydro-2/7-pyran-4-carboxamide 2.4 g (54%).
8-Chloro-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazine:
To a solution of A/-((3-chloropyrazin-2-yl)methyl)tetrahydro-2/-/-pyran-4-carboxamide (2.5 g, 9.8 mmol) in anhydrous 1,4-dioxane (20 mL) was added phosphoryl chloride (3.4 g, 22 mmol). The reaction was stirred at 80°C for 2 hours. Then the solution was cooled and poured into water (100 mL), pH was adjusted to 8-9 by the addition of saturated aqueous K2CO3. The crude mixture was extracted with ethyl acetate (2*100 mL). The combined organic phases were washed with brine (50 mL), dried over Na2SO4 and concentrated in vacuo. The residue was purified by flash chromatography using a gradient of petroleum etherand ethyl acetate to yield 8-chloro-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazine
2.1 g (90%).
3-(Tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one:
To a solution of 8-ch!oro-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazine (2.1 g, 8.8 mmol) in 1,4-dioxane (20 mL) was added 2 M aq. HCl (10 mL). The solution was stirred at 80°C for 2 hours. The mixture was cooled and pH was adjusted to 8-9 by addition of saturated aqueous K2CO3 The crude mixture was concentrated in vacuo and the residue was dissolved in methanol (150 mL) and filtered. The filtrate was concentrated in vacuo and the residue was purified by flash chromatography using a mixture of dichloromethane and methanol (10:1) to give 3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one 1.6 g (81%).
1H NMR (DMSO-ds, 400 MHz): 5 10.55 (s, 1 H). 7.63 (s, 1 H), 7.39 (d, J = 6.0 Hz, 1 H), 6.60 (s, 1H), 3.91-3.88 (m, 2H), 3.49-3.42 (m, 2H), 3.34-3.29 (m, 1H), 1.82-1.72 (m, 4H).
LC-MS: (m/z) 220.1 (MH+) tR (minutes, method 3) = 1.37 minutes
A/-((3-Chloropyrazin-2-yl)methyl)cyclopropanecarboxamide:
Cl ο
To a solution of of (3-chloropyrazin-2-yl)methanamine dihydrochloride (4.0 g, 19 mmol) in anhydrous DMF (20 mL) was added Et3N (1.9 g, 18.5 mmol). The mixture was cooled to 0°C and cyclopropanecarbonyl chloride (2.3 g, 22 mmol) was added dropwise. The reaction was stirred at 0°C for 0.5 hours. The reaction mixture was diluted with water (50 mL), extracted with ethyl acetate (2*100 mL). The combined organic phases were washed with brine (40 mL), dried over Na2SO4 and concentrated in vacuo. The residue was purified by flash chromatography eluting with petroleum ether/ethyl acetate 2/1 to yield A/-((3chloropyrazin-2-yl)methyl)cydopropanecarboxamide 3.3 g (85%).
8-Chloro-3-cyclopropylimidazo[1,5-a]pyrazine;
To a solution of A/-((3-chloropyrazin-2-yl)methyl)cyclopropanecarboxamide (3.3 g, 15.6 mmol) in anhydrous 1,4-dioxane (30 mL) was added phosphoryl chloride (5.3 g, 35 mmol). The reaction was stirred at 80°C for 2 hours. Then the solution was cooled on an ice-bath and poured into water (50 mL). The pH was adjusted to 8-9 by addition of saturated aqueous K2CO3. The mixture was extracted with ethyl acetate (2*50 mL). The combined organic phases were washed with brine (50 mL), dried over Na2SO4 and concentrated in vacuo. The residue was purified by flash chromatography using petroleum ether/ethyl acetate 3:1 to yield 8-chloro-3-cyclopropylimidazo[1,5-a]pyrazine 2.4 g (80%).
3-Cyclopropylimidazo[1,5-a]pyrazin-8(7H)-one:
To a solution of 8-chloro-3-cyclopropylimidazo[1,5-a]pyrazine (2.5 g, 13 mmol) in 1,4-dioxane (20 mL) was added 2 M aq. HCl (10 mL). The solution was stirred at 80DC for 2hrs. The mixture was cooled on an ice-bath and pH adjusted to 8-9 by addition of saturated aqueous K2CO3. The mixture was concentrated in vacuo and the residue was dissolved in methanol (150 mL) and filtered. The filtrate was concentrated in vacuo and the residue was purified by flash chromatography using dichloromethane/methanol 10/1) to afford 3cyc!opropylimidazo[1,5-a]pyrazin-8(7/-/)-one 1.9 g (83%).
1H NMR (DMSO-d6, 400 MHz): δ 10.49 (s, 1H), 7.54 (s, 1H), 7.41 (d. J= 5.6 Hz, 1H), 6.61 (d, J = 5.6 Hz. 1H), 2.29-2.24 (m, 1H), 0.99-0.89 (m, 4H).
LC-MS: (mlz) 176.1 (MH*) tR (minutes, method 1) = 1.04 minutes
N-((5-Bromo-3-methoxypyrazin-2-yl)methyl)tetrahydro-2H-pyran-4-carboxamide:
o o
O
A solution of NaNO2 (972 mg, 14.09 mmol) in H2O (100 mL) was added to a stirred solution of A/-((5-amino-3-methoxypyrazin-2-yl)methyl)tetrahydro-2/-/-pyran-4-carboxamide (2.5 g, 9.4 mmol) in 40% aq. HBr (33 mL) at 0°C. After stirring for 1.5 hrs, CuBr(2.02 g, 14.1 mmol) was added and the mixture was stirred at 70°C for 1 hour. The pH value was adjusted to pH 8 by addition of saturated aqueous NaHCO3. The mixture was filtered and the filtrate was concentrated in vacuo. The residue was purified by flash chromatography using a gradient of Petroleum ether and ethyl acetate to yield /\/-((5-bromo-3-methoxypyrazin-2yl)methyl)tetrahydro-2/7-pyran-4-carboxamide 800 mg (25%).
LC-MS: (mlz) 331.8 (MH*) îr (minutes, method 2) - 0.723 minutes
6-Bromo-8-methoxy-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazine:
To a solution of A/-((5-bromo-3-methoxypyrazin-2-yl)methyl)tetrahydro-2/-/-pyran-4carboxamide (800 mg, 2.42 mmol) in 1,4-dioxane (30 mL) was added phosphoryl chloride (3.8 g, 25 mmol) at O’C. The mixture was heated to 70°C and stirred for 1 hour. The mixture was concentrated in vacuo and the residue was diluted with dichloromethane (100 mL) and ice-water (60 mL). The pH value was adjusted to pH 8 by addition of saturated aqueous NaHCO3. The organic phase was separated and aqueous phase was extracted with dichloromethane (3*30 mL). The combined organic phases were dried and concentrated in vacuo. The residue was purified by flash chromatography using a gradient of dichloromethane and methanol to yield 6-bromo-8-methoxy-3-(tetrahydro-2/-/-pyran-4yl)imidazo[1,5-a]pyrazine 500 mg (66%).
LC-MS: (m/z) 313.7 (MH*) tR (minutes, method 2) = 0.740 minutes
6-Bromo-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one:
''Ό O
To a solution of 6-bromo-8-methoxy-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazine (200 mg, 0 641 mmol) in dichloromethane (30 mL) was added boron tribromide (1.61 g, 6.41
1S mmol) at 0°C. The reaction was warmed to 20°C and stirred for 3 hours. The solution was quenched with water (2 mL) at 0°C. The reaction was concentrated in vacuo and the residue was purified by flash chromatography using a gradient of dichloromethane and methanol to yield 6-bromo-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one 130 mg (68%).
LC-MS: (m/z) 299.7 (MH+) tR (minutes, method 2) = 0.730 minutes
2-methoxy-6-methyIpyrazine
Cl ’o
To a suspension of 2-chloro-6-methylpyrazine (24 g, 186.7 mmol) in anhydrous MeOH (240 mL) was added NaOMe (12.1 g, 224 mmol). The mixture was stirred at 60-70°C for 16 hours. The mixture was cooled and filtered. The filtrate was concentrated in vacuo to give 2methoxy-6-methylpyrazine (22 g, 95% yield). 1H NMR (CDCI3400 MHz): <5 7.98 (s, 1H), 7.94 (s, 1 H), 3.91 (s, 3H), 3.40 (s, 3H). LC-MS: tR = 1.47 min (method 14), m/z = 124.8 [M + H]+.
3-meth oxy-5-methylpyrazine 1-oxide
To a solution of 2-methoxy-6-methylpyrazine (21.3 g, 171.6 mmol) in AcOH (150 mL) was added NaBOzH2O2-3H2O (31.7 g, 205.9 mmol). The mixture was stirred at 80°C for 16 hours. The mixture was cocentrated in vacuo and diluted with 2 M aq. NaOH (300 mL). The mixture was extracted with EtOAc (200 mL * 4). The organic layer was washed with brine (100 mL), dried over Na2SO4 and concentrated in vacuo to give 3-methoxy-5-methylpyrazine 1-oxide (14.4 g, 60% yield).
3-meth oxy-5-methylpyrazine-2-carbonitrile
To a mixture of 3-methoxy-5-methylpyrazine 1-oxide (10 g, 71.4 mmol) in MeCN (200 mL) was added TMSCN (24.8 g, 249.8 mmol) and triethylamine (36.1 g, 356.8 mmol), ZnBr2 (32.1 g, 142.7 mmol). The mixture was stirred at 85-90°C for 16 hours. The mixture was concentrated in vacuo. The residue was diluted with DCM (500 mL) and filtered. The filtrate was washed with water (300 mL) and brine (200 mL). The organic layer was dried over Na2SO4 and concentrated in vacuo. The residue was purified by silica gel chromatography (petroleum ether:ethyl acetate=5:1) to give 3-methoxy-5-methylpyrazine-2-carbonitrile (4.1 g, 38% yield).
tert-butyl ((3-methoxy-5-methylpyrazin-2-yl)methyl)carbamate
To a solution of 3-methoxy-5-methylpyrazine-2-carbonitrile (6.22 g, 41.7 mmol) in MeOH (100 mL) was added (Boc)20 (13.65 g, 62.6 mmol) and Raney Ni (2.0 g). The mixture was stirred at 20-25’C under H2 (45 psi) for 16 hours. The mixture was filtered and the filtrate was concentrated in vacuo. The residue was purified by silica gel chromatography (Petroleum ethenethyl acetate=5:1) to give tert-butyl ((3-methoxy-5-methylpyrazin-2yl)methyl)carbamate (7.7 g, 72% yield).
LC-MS: fi, = 0 70 min (method 15). m/z = 254 0 [M + Hf.
(3-methoxy-5-methylpyrazin-2-yl)methanamine
To a solution of tert-butyl ((3-methoxy-5-methylpyrazin-2-yl)methyl)carbamate (7.7 g, 30.3 mmol) in THF (50 mL) was added TFA (20 mL). The mixture was stirred at 80°C for 2 hours. The mixture was concentrated in vacuo. The residue was diluted with 2 M aq. NaOH (200 mL), extracted with DCM (100 mL * 2). The organic layer was washed with brine (50 mL), dried over Na2SO4 and concentrated in vacuo to give (3-methoxy-5-methylpyrazin-2yl)methanamine (2.5 g, 54% yield).
1H NMR (CDCI3 400 MHz): δ 7.90 (s, 1 H), 3.96 (S, 3H), 3.93 (s, 2H), 2.42 (S, 3H) , 1.69 (s, 2H).
LC-MS: tR = 0.73 min(method 16), mlz = 154.2 [M + H]*.
COMPOUNDS OF THE INVENTION:
Example 1
7-(3-Fluorobenzyl)-3-propylimidazo[1,5-a]pyrazin-8(7H)-one:
To a solution of 3-propylimidazo[1,5-a]pyrazin-8(7H)-one (1.2 g, 6.8 mmol) in DMF (10 mL) was added potassium carbonate (1.4 g, 10 mmol) and 1-(bromomethyl)-3-fluorobenzene (1.54 g, 8.13 mmol). The mixture was stirred at 60-70°C for 2 hrs and then cooled to room température. To the reaction was added water (75 mL) and it was extracted with ethyl acetate (2*50mL). The combined organic phases were washed with brine, dried and concentrated in vacuo. The residue purified by flash chromatography to yield 1.5 g (78%) of 7-(3-fluorobenzyl)-3-propylimidazo[1,5-a]pyrazin-8(7/-/)-one.
Ή NMR (DMSO-dË. 400 MHz): <57.70 (s, 1H), 7.46-7 37 (m, 2H). 7.17-7.09 (m, 3H), 7.00 (d, >6.0 Hz, 1H), 5.02 (s, 2H), 2.83 (t, 2H), 1.75-1.66 (m, 2H), 0.91 (t, 3H).
LC-MS. (m!z) 286.1 (MH*) tR (minutes, method 3) = 2.19 minutes
Example 2
6-BenzyI-7-(3-fluorobenzyl)-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)one:
A mixture of 6-benzyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one (200 mg, 0.647 mmol), 1-(bromomethyI)-3-fluorobenzene (159 mg, 840 pmol) and potassium carbonate (179 mg, 1.29 mmol) in DMF (6 mL) was stirred at 60°C for 12 hours. The reaction mixture was concentrated in vacuo and the residue was diluted with dichloromethane (20 mL) and washed with water (3*5 mL). The combined organic phases were dried, filtered and concentrated in vacuo. The residue was purified by preparative TLC, eluting with petroleum ether and ethyl acetate 1:2, to yield 6-benzyl-7-(3fluorobenzyl)-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one 80 mg (28%).
1H NMR (CDCi31 400 MHz): <5 7.97 (s, 1 H), 7.39-7.30 (m, 4 H), 7.17 (d, >7.53 Hz, 2 H), 6.94-6.92 (m, 2 H), 6.83 (d, >9.54 Hz, 1 H), 6.74 (s, 1 H), 5.06 (s., 2 H), 4.12 (d, >12.05 Hz, 2 H), 3.74 (s, 2 H), 3.58 - 3.52 (m, 2 H), 3.03 - 3.09 (m, 1 H), 2.19 - 2.09 (m, 2 H), 1.89 (d, >13.55 Hz, 2 H).
LC-MS: (m/z) 418.2 (MH+) tR (minutes, method 3) = 2.69 minutes
Example 3
Oo
6-Benzyl-7-(cyclohexylmethyl)-3-(tetrahydro-2tf-pyran-4-yl)imidazo[1,5-a]pyrazin8(7H)-one:
A mixture of 6-benzyl-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (60 mg. 0.19 mmol), (bromomethyl)cyclohexane (52 mg, 0.29 mmol) and potassium carbonate (54 mg, 0.39 mmol) in DMF (10 mL) was stirred at 75°C for 12 hours. The reaction mixture was concentrated in vauo. The residue was diluted with dichloromethane (20 mL) and washed with water (3*5 mL). The combined organic phases were dried, filtered and concentrated in vacuo. The residue was purified by préparative TLC, eluting with petroleum ether and ethyl acetate 1:2, to yield 6-benzyl-7-(cyclohexylmethyl)-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5a]pyrazin-8(7H)-one 15 mg (8.1%).
1H NMR (CDCI3, 400 MHz): 5 7.87 (s, 1 H), 7.42-7.30 (m, 3 H), 7.19 (d, J=7.34 Hz, 2 H), 6.65 (s, 1 H), 4.11 (d, J=11.25 Hz, 2 H), 3.90 (s, 2 H), 3.66 (d, J=6.36 Hz, 2 H), 3.54 (t, J=10.76 Hz, 2 H), 3.05-2.99 (m, 1 H), 2.18 - 2.04 (m, 2 H), 1.86 (d, J=13.94 Hz, 2 H), 1.63 1.77 (m, 7 H), 1.18-1.15 (m, 2 H), 1.04-1.01 (m, 2 H).
LC-MS: (m!z) 406.2 (MH+) tR (minutes, method 4) = 2.38 minutes
Example 4
7-(Cyclohexylmethyl)-6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin8(7W)-one:
A mixture of 6-methyl-3-(tetrahydro-2/7-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (50 mg, 0.21 mmol), (bromomethyl)cyclohexane (57 mg, 0.32 mmol) and potassium carbonate (59 mg, 0.43 mmol) in DMF (2 mL) was stirred at 60°C for 12 hours. The reaction mixture was concentrated in vacuo. The residue was diluted with dichloromethane (20 mL) and washed
Example 8 ο
74CyclôhexylmethyI)-3-cyclopropylimidazo[1,5-â]pyrazin-S(7H)-one:
Το 3 solution of 3-cyclopropylimidazo[1,5-a]pyrazin-8(7H)-one (300 mg, 1.71 mmol) in anhydrous DMF (5 mL) was added K2CO3 (355 mg, 2.57 ' mmoi) and (bromomethyl)cyclohexane (363 mg, 2.05 mmol). The reaction was stirred at 65°C for 16 heurs. The reaction mixtuie was filtered and the filtrate was purified by P'eparativa LC-MS to yield 7-(cyclohexylmethy!)-3-cyclopropylimidazo[1,5-a]pyrazin-8(7H)one 195 mg (42%).
Ή NîvlR {DMSO-d.31400 MHz): ΰ 7.53-7.49 (m, 2H), 6.84 (d, J = 6.0 Hz, 1 H), 3.59 (d, J = 7.6Hz, ?H) 2.27-2 25 (m, 1H), 1.68-1.55 (m, 6H). 1.10-0.89 (m, 9H).
LG-MS. \nuz) Z72.2 (MH*) tR (minutes, meihod 3) = 2.40 minutes
Exemple 9 o
7(3-FI,.iorobenr.yl)-3-(tetrahydro-2H-pyran-4-yl)iniidazo[1,5-a]pyrazin-8(7H)-one:
Ίο a solution of 3-(tetrahydro-2H-pycarM-y!)imidazo[1,5-a]pyrazin-8(7H)-one (200 mg, 0.91 rnmo!) in anhydreus DMF (5 mL) was added K2CO3 (189 mg, 1.37 mmol) and 1(brcmornethyl)-3-fluorobenzene (207 mg, 1.10 mmol). The reaction mixture was stirred at
60°C for 16 hours. The mixture was filtered and the filtrate was purified by preparative LCMS to afford 7-(3-fluorobenzyl)-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one 190 mg (64%).
, ’H NMR (DMSO-d8,400 Mhz): 5 7.68 ts, iH), 7.54 (d, J = 6.0 Hz, 1H), 7.36-7.33 (m, 1H), 7,14-7.09 (m, 3H), 6.99 (d, J - 6.Ü Hz, 1 H), 4.99 (s, 2H), 3.91-3.88 (m, 2H), 3.48-3.42 (m,
2H), 3.30-3.2S (m, 1H). 1.81-1.73 (m. 4H).
LC-MS: (m/z) 328.1 (MIT) tR (minutes, method 1) = 1.92 minutes
Example 10
7-(Cyclopentylmethyl)-3-(tetrahydro-2H-pyran-4-yI)imidazo[1,5-a]pyrazin-8(7H)-one:
To a solution of 3-(tetrahydro-2/7-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one (400 mg, 1.82 mmol) in anhydrous DMF (5 mL) was added K2CO3 (503 mg, 3.64 mmol) and (bromomethyl)cyclopentane (445 mg, 2.73 mmol). The reaction mixture was stirred at 60°C for 16 hours. The mixture was filtered and the filtrate was purified by préparative LC-MS to afford 7-(cyc1opentylmethyl)-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5a]pyrazin-8(7/7)-one 290 mg (53%).
1H NMR (DMSO-d6, 400 Mhz): δ 7.62 (s, 1 H), 7.49 (d, J = 6.0 Hz, 1H), 6.90 (d, J = 6.0 Hz, 1H), 3.91-3.88 (m, 2H), 3.69 (d, J = 7.6Hz, 2H), 3.48-3.43 (m, 2H), 3.42-3.31 (m, 1H), 2.272.24 (m, 1H), 1.78-1.73 (m, 4H), 1.58-1.44 (m, 6H), 1.21-1.20 (m, 2H).
LC-MS: (m/z) 302.2 (MH*) tR (minutes, method 3) = 2.29 minutes
Example 11
7-(Cyclohexylmethyl)-3-(tetrahydro-2H-pyran-4-yï)imidazo[1,5-a]pyrazin-8(7H)-orie:
To a solution of 3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (300 mg, 1.37 mmol) in anhydrous DMF (5 mL) was added K2CO3 (379 mg, 2.74 mmol) and (bromomethyl)cyclohexane (364 mg, 2.06 mmol). The reaction mixture was stirred at 60°C for 16 hours. The mixture was filtered and the filtrate was purified by préparative LC-MS to yield 7-(cyclohexylmethyl)-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,518771
a]pyrazin-8(7H)-one 240 mg (55%).
1H NMR (DMSO-de, 400 Mhz): δ 7.62 (s, 1 H), 7.47 (d, J = 6.0 Hz, 1 H), 6.84 (d, J = 6.2 Hz, 1H), 3.91-3.88 (m, 2H), 3.60 (d, J = 7.2 Hz. 2H), 3.48-3.42 (m, 2H), 3.30-3.29 (m, 1H), 1.781.52 (m, 10H), 1.10-1.06 (m, 3H), 0.93-0.91 (m, 2H).
LC-MS: (mlz) 316.2 (MH’) tR (minutes, method 3) = 2.44 minutes.
Example 12
7-(Cycloheptylmethyl)-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one:
To a solution of 3-(tetrahydro-2/-/-pyran^-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one (300 mg, 1.37 mmol) in anhydrous DMF (4 mL) was added K2CO3 (568 mg, 4,11 mmol) and cycloheptylmethyl methanesulfonate (565 mg, 2.74 mmol). The reaction mixture was stirred at 95°C for 16 hours. The mixture was filtered and the filtrate was purified by préparative LC-MS to afford 7-(cycloheptylmethyl)-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5a]pyrazin-8(7/-/)-one 140 mg (30%).
1H NMR (DMSO-d61 400 MHz): 5 7.62 (s, 1 H), 6.48 (d, J = 5.6 Hz, 1 H), 6.87 (d, J = 6.0 Hz, 1H), 3.91-3.88 (m, 2H), 3.59 (d, J= 7.6 Hz, 2H), 3.48-3.42 (m, 2H), 3.31-3.26 (m, 1H), 1.901.73 (m, 5H), 1.57-1.43 (m, 10H), 1.13-1.11 (m, 2H).
LC-MS: (m/z) 330.2 (MH’) tR (minutes, method 3) = 2.58 minutes
Example 13
7-(Cycloheptylmethyl)-3-cyclopropylimidazo[1,5-a]pyrazin-8(7H)-one:
To a solution of 3-cyclopropylimidazo[1,5-a]pyrazin-8(7/-/)-one (300 mg, 1.71 mmol) in anhydrous DMF (4 mL) was added K2CO3 (709 mg, 5.1 mmol) and cycloheptyimethyl methanesulfonate (706 mg, 3.42 mmol). The reaction mixture was stirred at 95°C for 16 hours. The mixture was filtered and the filtrate was purified by préparative LC-MS to afford 7-(cycloheptylmethyl)-3-cyclopropylimidazo[1,5-a]pyrazin-8(7/7)one 115 mg (24%).
1H NMR (DMSO-ds, 400 MHz): δ 7.55-7.52 (m, 2H), 6.89 (d, J = 6.0 Hz, 1 H), 3.61 (d, J = 7.6 Hz, 2H), 2.32-2.27 (m, 1H), 1.91 (brs, 1H), 1.91-1.02 (m, 12H), 1.01-0.91 (m, 4H).
LC-MS: (m/z) 286.2 (MH+) tR (minutes, method 3) = 2.54 minutes.
Example 14
O
7-(4-Chlorobenzyl)-6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)one:
A mixture of 6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one (100 mg, 0.429 mmol), 1-(bromomethyl)-4-chlorobenzene (132 mg, 0.643 mmol) and Cs2CO3 (280 mg, 0.857 mmol) in DMF (2.0 mL) was stirred at 70°C for 12 hours. The reaction mixture was filtered and the filtrate was concentrated in vacuo. The residue was purified by préparative LC-MS to afford 7-(4-chlorobenzyl)-6-methyl-3-(tetrahydro-2/-/-pyran-4yl)imidazo[1,5-a]pyrazin-8(7H)-one 53 mg (34%).
Ή NMR (CDCI3, 400 MHz): δ 7.93 (s, 1 H), 7.30 (d, J = 8.4 Hz, 2H), 7.16 (d, J = 8.4 Hz, 2H),
6.76 (s, 1H), 5.20 (s, 2H), 4.13 (d, J= 10.8 Hz, 2H), 3.62-3.56 (m, 2H), 3.12 - 3.05 (m, 1H),
2.18 (s, 3H), 2.16-2.09 (m, 2H), 1.89 (d, J = 13.2 Hz, 2H).
LC-MS: (m/z) 358.1 (MH4) tR (minutes, method 3) = 2.46 minutes
Example 15
O
6-Bromo-7-(3-fluorobenzyl)-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)one:
A mixture of 6-bromo-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (100 mg, 0.335 mmol), 1-(bromomethyl)-3-fluorobenzene (95 mg, 0.50 mmol) and K2CO3 (93 mg, 0.67 mmol) in DMF (2.0 mL) was stirred at 60°C for 12 hours. The reaction mixture was concentrated in vacuo. The residue was purified by préparative LC-MS to give 6-bromo-7-(3fluorobenzyl)-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one 30 mg (22%).
1H NMR (CDCI31 400 MHz): 5 7.95 (s, 1H), 7.34-7.27 (m, 1H), 7.18 (s, 1H), 7.11 (d, J = 7.6 Hz, 1H), 7.03 - 6.99 (m, 2H), 5.39 (s, 2H), 4.13 (d, J = 12.0 Hz, 2H). 3.62 - 3.56 (m, 2H), 3.11 - 3.05 (m, 1H), 2.18-2.08 (m, 2H), 1.88 (d, 14.0 Hz, 2H).
LC-MS: (miz) 408.0 (MH4) tR (minutes, method 3) = 2.65 minutes
Example 16 o
7-Benzyl-6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one:
A mixture of 6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (100 mg, 0.429 mmol), (bromomethyl)benzene (110 mg, 0.643 mmol) and K2CO3 (119 mg, 0.857 mmol) in DMF (1.0 mL) was stirred at 60°C for 3 hours. The mixture was filtered and the filtrate was concentrated in vacuo. The residue was purified by preparative LC-MS to yield 7benzyl-6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one 39 mg (28%).
1H NMR (CDCI3. 400 MHz): δ 7.93 (s. 1H). 7 35 - 7.29 (m, 3H), 7.21 (d. J = 7.6 Hz. 2H). 6.75 (s, 1H), 5.25 (s, 2H), 4.13 (d, J= 11.6 Hz, 2H), 3.61 -3.56 (m, 2H), 3.13-3.06 (m, 1H), 2.19 (s, 3H), 2.15 - 2.08 (m, 2H), 1.89 (d, J = 13.2 Hz, 2H).
LC-MS: (m/z) 324.2 (MH*) tR (minutes, method 3) = 2.25 minutes
Example 17
7-(2-Fluorobenzyl)-6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)one:
A mixture of 6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (100 mg, 0.429 mmol), 1-(bromomethyl)-2-fluorobenzene (122 mg, 0.643 mmol) and Cs2CO3 (279 mg, 0.857 mmol) in DMF (2.0 mL) was stirred at 70°C for 1 hour. The mixture was filtered and the filtrate was concentrated in vacuo. The residue was purified by preparative LC-MS to afford 7-(2-fluorobenzyl)-6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)one 49 mg (33%).
1H NMR (CDCI3, 400 MHz): δ 7.93 (s, 1H), 7.27 - 7.23 (m, 1H), 7.11 - 7.06 (m, 3H), 6.77 (s, 1H), 5.28 (s, 2H), 4.13 (d, J = 10.4 Hz, 2H), 3.62-3.56 (m, 2H), 3.12 - 3.07 (m, 1H), 2.19 (s, 3H), 2.16-2.10 (m, 2H), 1.89 (d, J = 12.0 Hz, 2H).
LC-MS: (m/z) 342.1 (MH+) tR (minutes, method 3) = 2.30 minutes
Example 18
7-(3-Chlorobenzyl)-6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)one:
A mixture of 6-methyl-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (100 mg, 0 429 mmol), 1-(bromomethyl)-3-chlorobenzene (132 mg, 0.643 mmol) and K2CO3 (119 mg, 0.857 mmol) in DMF (1.0 mL) was stirred at 65°C for 12 hours. To the mixture was added Cs2CO3 (280 mg, 0.857 mmol) and the reaction was stirred at 80°C for another 1 hour. The reaction mixture was filtered and the filtrate was concentrated in vacuo. The residue was purified by preparative LC-MS to afford 7-(3-chlorobenzyl)-6-methyl-3-(tetrahydro-2/7-pyran-
4-yl)imidazo[1,5-a]pyrazin-8(7/7)-one 49 mg (32%).
1H NMR (CDCI3, 400 MHz): δ 7.92 (s, 1H), 7.25 - 7.24 (m, 2H), 7.16 (s, 1H), 7.10 - 7.07 (m, 1H), 6.75 (s, 1H), 5.19 (s, 2H). 4.11 (d, J= 10.4 Hz, 2H), 3.60 - 3.54 (m, 2H), 3.12 - 3.05 (m, 1H), 2.16 (s, 3H), 2.14-2.07 (m, 2H), 1.87 (d, J= 12.0 Hz, 2H).
LC-MS: (mlz) 358.1 (MH*) tR (minutes, method 3) = 2.44 minutes
Example 19
7-(2-Chlorobenzyl)-6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)one:
A mixture of 6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one (100 mg, 0.429 mmol), 1-(bromomethyl)-2-chlorobenzene (132 mg, 0.643 mmol) and Cs2CO3 (279 mg, 0.857 mmol) in DMF (2.0 mL) was stirred at 80°C for 12 hours. The mixture was filtered and the filtrate was concentrated in vacuo. The residue was purified by preparative LC-MS to yield 7-(2-chlorobenzyl)-6-methyl-3-(tetrahydro-2/7-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/7)one 55 mg (36%).
Ή NMR (CDCI31 400 MHz): 57.95 (s, 1H), 7.42-7.40 (m, 1H), 7.25-7.20 (m, 2H), 6.93 (d, J = 7.2 Hz. 1H), 6.80 (s, 1H), 5.32 (s, 2H), 4.14 (d, J = 10.8 Hz, 2H), 3.63 - 3.57 (m, 2H), 3.14-3.07 (m, 1H), 2.20-2.10 (m, 2H), 2.13 (s, 3H), 1.91 (d, 13.2 Hz, 2H).
LC-MS: (m!z) 358.1 (MH*) tR (minutes, method 3) = 2.46 minutes
Example 20
N
7-(3-Methoxybenzyl)-6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)one:
A mixture of 6-methyl-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (100 mg, 0.429 mmol), 1-(bromomethyl)-3-methoxybenzene (129 mg, 0.643 mmol) and Cs2CO3 (280 mg, 0.857 mmol) in DMF (1.0 mL) was stirred at 80°C for 12 hours. The reaction mixture was filtered and the filtrate was concentrated in vacuo. The residue was purified by préparative LC-MS to yield 7-(3-methoxybenzyl)-6-methyl-3-(tetrahydro-2H-pyran-4yl)imidazo[1,5-a]pyrazin-8(7H)-one 68 mg (45%).
Ή NMR (CDCI3, 400 MHz): δ 7.92 (s, 1 H), 7.27 - 7.23 (m, 1 H), 6.82 - 6.77 (m, 2H), 6.74 (s, 2H), 5.21 (s, 2H), 4.13 (d, J = 10.8 Hz, 2H), 3.78 (s, 3H), 3.62 - 3.56 (m, 2H), 3.12 - 3.08 (m, 1H), 2.19 (s, 3H), 2.19-2.10 (m. 2H). 1.89 (d, J = 13.2 Hz, 2H).
LC-MS: (m/z) 354.2 (MH+) tR (minutes, method 3) = 2.28 minutes
Example 21
6-Methyl-7-(2-methylbenzyl)-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)one:
A mixture of 6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (100 mg, 0.429 mmol), 1-(bromomethyl)-2-methylbenzene (119 mg, 0.643 mmol) and K2CO3 (119 mg, 0.857 mmol) in DMF (2.0 mL) was stirred at 60°C for 12 hours. To the mixture was added additionally Cs2CO3 (280 mg, 0.86 mmol) and the reaction stirred at 70°C for another 13 hours. The reaction mixture was filtered and the filtrate was concentrated in vacuo. The residue was purified by préparative LC-MS to afford 6-methyl-7-(2-methylbenzyl)-3(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one 23 mg (16%).
1H NMR (CDCI3. 400 MHz): 57.93 (s, 1H), 7.21 - 7.12 (m, 3H), 6.80 (s, 1H), 6.78 (d, J = 7.6 Hz, 1H), 5.18 (s, 2H), 4.15 (d, J = 10.8 Hz, 2H), 3.63-3.57 (m, 2H), 3.15-3.09 (m, 1H), 2.40 (s, 3H), 2.20 - 2.13 (m, 2H), 2.11 (s, 3H), 1.92 (d, J= 13.2 Hz, 2H).
LC-MS: (mlz) 338.2 (MH*) îr (minutes, method 3) = 2.37 minutes
Example 22 o
6-Methyl-7-(4-methylbenzyl)-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)one:
A mixture of 6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one (100 mg, 0.429 mmol), 1-(bromomethyl)~4-methylbenzene (119 mg, 0.643 mmol) and Cs2CO3 (280 mg, 0.857 mmol) in DMF (2.0 mL) was stirred at 70°C for 12 hours. The mixture was filtered and the filtrate was concentrated in vacuo. The residue was purified by préparative LC-MS to afford 6-methyl-7-(4-methylbenzyl)-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)one 68 mg (47%).
1H NMR (CDCI3, 400 MHz): δ 7.92 (s, 1 H), 7.14 - 7.09 (m, 4H), 6.74 (s, 1 H), 5.20 (s. 2H),
4.13 (d, J = 10.4 Hz, 2H), 3.62 - 3.56 (m, 2H), 3.11 - 3.06 (m, 1H), 2.32 (s, 3H), 2.19 (s, 3H), 2.19-2.08 (m, 2H), 1.88 (d, J = 13.2 Hz, 2H).
LC-MS: (m/z) 338.2 (MH+) tR (minutes, method 3) = 2.41 minutes.
Example 23 ο
7-(4-Methoxybenzyl)-6-methyl-3-{tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazjn-8(7H)one:
A mixture of 6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (100 mg, 0.43 mmol), 1-(bromomethyl)-4-methoxybenzene (129 mg, 0.643 mmol) and Cs2CO3 (280 mg, 0.857 mmol) in DMF (2.0 mL) was stirred at 70°C for 12 hours. The mixture was filtered and the filtrate was concentrated in vacuo. The residue was purified by préparative LC-MS to afford 7-(4-methoxybenzyl)-6-methyl-3-(tetrahydro-2/7-pyran-4-yl)imidazo[1,5-a]pyrazin8(7H)-one 60 mg (39%).
’H NMR (CDCIa, 400 MHz): δ 7.93 (s, 1 H), 7.17 (d, J = 8.4 Hz, 2H), 6.86 (d, J = 8.4 Hz, 2H), 6.73 (s, 1H), 5.17 (s, 2H), 4.13 (d, J = 10.0 Hz, 2H), 3.79 (s, 3H), 3.58 (t, J = 12.0 Hz, 2H), 3.11 -3.05 (m, 1H), 2.21 (s, 3H), 2.18-2.08 (m, 2H), 1.88 (d, J= 13.6 Hz, 2H).
LC-MS: (m/z) 354.2 (MH') tR (minutes, method 3) = 2.26 minutes.
Example 24 o
7-(4-Fluorobenzyl)-6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)one:
A mixture of 6-methyl-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (100 mg, 0.429 mmol), 1-(bromomethyl)-4-fluorobenzene (122 mg, 0.643 mmol) and Cs2CO3 (279 mg, 0.857 mmol) in DMF (2.0 mL) was stirred at 70°C for 12 hours. The mixture was filtered and the filtrate was concentrated in vacuo. The residue was purified by préparative LC-MS to yield 7-(4-fluorobenzyl)-6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7A7)one 30 mg (21%).
'H NMR (CDCI3, 400 MHz): 5 7.93 (s, 1 H), 7.22 -7.19 (m, 2H), 7.04-7.00 (m, 2H), 6.75 (s,
H), 5.20 (s, 2H), 4.13 (d, J = 11.2 Hz, 2H), 3.62-3.60 (m, 2H), 3.17 - 3.06 (m, 1H), 2.19 (s, 3H), 2.14-2.08 (m, 2H), 1.88 (d, J= 13.6 Hz, 2H).
LC-MS: (mlz) 342.1 (MH*) tR (minutes, method 3) = 2.30 minutes
Example 25 o H
6-Methyl-7-(3-methylbenzyl)-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)one:
A mixture of 6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (100 mg. 0.429 mmol), 1-(bromomethyl)-3-methylbenzene (119 mg, 0.643 mmol) and Cs2CO3 (280 mg, 0.857 mmol) in DMF (1 mL) was stirred at 80°C for 12 hours. The mixture was filtered and the filtrate was concentrated in vacuo. The residue was purified by préparative LC-MS to afford 6-methyl-7-(3-methylbenzyl)-3-(tetrahydro-2/7-pyran-4-y!)imidazo[1,5-a]pyrazin-8(7H)one 62 mg (43%).
1H NMR (CDCI3, 400 MHz): δ 7.93 (s, 1H), 7.21 (t, J = 7.2 Hz, 1H), 7.08 (d, J = 7.6 Hz, 1H), 7.02 - 6.98 (m, 2H), 6.74 (s, 1H), 5.21 (s, 2H), 4.13 (d, J = 10.8 Hz, 2H), 3.62 - 3.56 (m, 2H), 3.12-3.07 (m, 1H), 2.33 (s, 3H), 2.19 (s, 3H), 2.19-2.09 (m, 2H), 1.89 (d, J= 13.2 Hz, 2H).
LC-MS: (mlz) 338.1 (MH*) tR (minutes, method 3) = 2.40 minutes.
Exampfe 26:
7-{3-fluorobenzyl)-6-methyl-3-(4-methyltetrahydro-2H-pyran-4-yl)imidazo[1(5-a]pyrazin8(7H)-one:
Step 1: To a solution of (3-methoxy-5-methylpyrazin-2-yI)methanamine (150 mg, 0.98 mmol) and 4-methyltetrahydro-2/7-pyran-4-carboxylic acid (212 mg, 1.5 mmol) in DCM (6 mL) was added HATU (670 mg, 1.8 mmol) and Et3N (198 mg, 1.96 mmol). The mixture was stirred at 20-25°C for 1 hour. The mixture was diluted with DCM (50 mL), washed with water (30 mL) and brine (30 mL). The organic layer was dried over Na2SO4 and concentrated in vacuo. The residue was purified by silica gel chromatography (petroleum ethecethyl acetate=3:1) to give A/-((3-methoxy-5-methylpyrazin-2-yl)methyl)-4-methyltetrahydro-2H-pyran-4-carboxamide (250 mg. 91% yield).
Step 2: To a solution of A/-((3-methoxy-5-methylpyrazin-2-yl)methyl)-4-methyltetrahydro-2Hpyran-4-carboxamide (300 mg, 1.07 mmol) in dioxane (5 mL) was added POCI3 (660 mg, 4.3 mmol). The solution was stirred at 80-90°C for 3 hours. The mixture was concentrated in vacuo, diluted with DCM (50 mL) and slowly added into water (30 mL). The organic layer was washed with brine (20 mL) and dried over Na2SO4, concentrated in vacuo to give 8methoxy-6-methyl-3-(4-methyltetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazine (250 mg, 89% yield).
Step 3: To a solution of 8-methoxy-6-methyl-3-(4-methyltetrahydro-2/-/-pyran-4yl)imidazo[1,5-a]pyrazine (200 mg, 0.77 mmol) in dioxane (10 mL) was added 2M HCI(aq) (10 mL). The solution was stirred at 80-90°C for 1 hour. The mixture was cooled and added saturated aqueous NaHCO3 (100 mL), extracted with DCM (100 mL χ 2). The organic layer was washed with brine (50 mL), dried over Na2SO4 and concentrated in vacuo to give 6methyl-3-(4-methyltetrahydro-2/7-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/7)-one (160 mg, 68% yield).
LC-MS: tR = 0.89 min (method 10), m/z - 248.3 [M + H]+.
Step 4: To a solution of 6-methyl-3-(4-methyltetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin8(7H)-one (200 mg, 0.81 mmol) and 1-(bromomethyl)-3-fluorobenzene (183 mg, 0.97 mmol) in anhydrous DMF (5 mL) was added K2CO3 (168 mg, 1.21 mmol). The mixture was stirred at 60-70°C for 16h. The mixture was cooled and diluted with water (20 mL), extracted with EtOAc(30 mL χ 2). The organic layer was washed with brine (20 mL), dried over Na2SO4 and concentrated in vacuo. The residue was purified by silica gel chromatography (petroleum etherethyl acetate=1:2) to give 7-(3-fluorobenzyl)-6-methyl-3-(4-methyltetrahydro-2/-f-pyran-
4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (90 mg, 31% yield) as a off-white solid.
1H NMR (CDCI3400 MHz): 5 7.94 (s, 1H), 7.33-7.28 (m, 1H), 7.02-6.91 (m, 4H), 5.22 (s, 2H), 3.85-3.80 (m, 2H), 3.73-3.67 (m, 2H), 2.45-2.41 (m, 2H), 2.17 (s, 3H), 1.86-1.79 (m, 2H),
1.49 (s, 3H).
LC-MS: iR = 2.46 min (method 3), m/z = 356.2 [M + H]+.
Example 27:
o
4-(7-(3-fluorobenzyl)-6-methyl-8-oxo-7,8-dihydroimidazo[1,5-a]pyrazin-3-yl)tetrahydro2H-pyran-4-carbonîtrile:
Step 1: To a sloution of (3-methoxy-5-methylpyrazin-2-yl)methanamine (100 mg, 0.65 mmol) and 4-cyanotetrahydro-2/7-pyran-4-carboxylic acid (152 mg, 0.98 mmol) in DCM (6 mL) was added HATU (447 mg, 1.18 mmol) and Et3N (132 mg, 1.31 mmol). The mixture was stirred at 20-25°C for 1 hour. The mixtue was diluted with DCM (30 ml), washed with water (20 mL) and brine (20 mL). The organic layer was dried over Na2SO4 and concentrated in vacuo. The residue was purified by silica gel chromatography(petroleum etherethyl acetate=1:1) to give 4-cyano-A/-((3-methoxy-5-methylpyrazin-2-yl)methyl)tetrahydro-2/-/-pyran-4-carboxamide (100 mg, 53% yield).
LC-MS: tR = 0.61 min (method 2), m/z = 290.9 [M + H]*.
Step 2: To a solution of 4-cyano-A/-((3-methoxy-5-methylpyrazin-2-yl)methyl)tetrahydro-2Hpyran-4-carboxamide (100 mg, 0.34 mmol) in dioxane (5 mL) was added POCI3 (330 mg, 2.15 mmol). The solution was stirred at 80-90’C for 2h. The mixture was cooled and slowly added into water (50 mL), extracted with EtOAc(30 mL χ 2). The organic layer was washed with brine (20 mL), dried over Na2SO4 and concentrated in vacuo to give 4-(8-methoxy-6methylimidazo[1,5-a]pyrazin-3-yl)tetrahydro-2/7-pyran-4-carbonitrile (80 mg, 85% yield).
Step 3: To a solution of 4-(8-methoxy-6-methylimidazo[1,5-a]pyrazin-3-yl)tetrahydro-2/-/pyran-4-carbonitrile (80 mg, 0.29 mmol) in dioxane (4 mL) was added 2M HCl(aq) (2 mL). The solution was stirred at 80-90°C for 2h. The mixture was concentrated in vacuo and added saturated aqueous NaHCO3 (50 mL). The mixtue was extracted with DCM (50 mL χ 2). The organic layer was washed with brine (20 mL) and concentated in vacuo to give 4-(6methyl-8-oxo-7,8-dihydroimidazo[1,5-a]pyrazin-3-yl)tetrahydro-2/-/-pyran-4-carbonitrile (70 with saturated aqueous NH4CI (0.5 mL) and evaporated under vacuum. The residue was dissolved in DCM (20 mL) and washed with water (10 mL). The organic layer was dried over Na2SO4 and evaporated. The residue was washed with EtOAc (3 mL) and filtered. The filter cake was dried under vacuum to give 7-(3-fluorobenzyl)-3-(4-hydroxytetrahydro-2/7-pyran-4yl)-6-methylimidazo[1,5-a]pyrazin-8(7/-/)-one (100 mg, 47% yield).
Step 3: To a solution of 7-(3-fluorobenzyl)-3-(4-hydroxytetrahydro-2H-pyran-4-yl)-6methylimidazo[1,5-a]pyrazin-8(7/-/)-one (80 mg, 0.22 mmol) in THF (5 mL) was added NaH (60% in minerai oil, 13.4 mg. 0.36 mmol) at 0°C. The mixture was stirred at 20°C for 30 minutes. Mel (64 mg, 0.45 mmol) was added at 0°C. The mixture was stirred at 20°C for 11.5 hours. The mixture was quenched with saturated aqueous NH4CI (0.5 mL) and evaporated under vacuum. The residue was dissolved in DCM (10 mL) and washed with water (4 mL). The organic layer was dried over Na2SO4 and evaporated. The residue was purified by préparative TLC (EtOAc) to give 7-(3-fluorobenzyl)-3-(4-methoxytetrahydro-2/7pyran-4-yl)-6-methylimidazo[1,5-a]pyrazin-8(7/7)-one (25 mg, 30% yield).
1H NMR (CDCI3, 400 MHz): δ 7.93 (s, 1 H), 7.36 (s, 1 H), 7.31 (dd, J = 8.0 Hz, J = 14.0 Hz, 1H), 7.03-6.92 (m, 3H), 5.23 (s, 2H), 3.91-3.80 (m, 4H), 3.07 (s, 3H), 2.38-2.31 (m, 2H), 2.17 (s, 3H), 2.14-2.10 (m, 2H).
LC-MS: fR = 2.73min (method 3), m/z = 372.1 [M + Hf.
Example 29:
7-(3-fluorobenzyl)-3-(4-fluorotetrahydro-2H-pyran-4-yl)-6-methylimidazo[1,5-a]pyrazin8(7H)-one:
Step 1: To a solution of 3-bromo-7-(3-fluorobenzyl)-6-methylimidazo[1,5-a]pyrazin-8(7H)-one (100 mg, 0.3 mmol) in dry THF (5 mL) was added n-BuLi (2.5 M, 0.15 mpL) (2.5 M in nhexane) dropwise. The mixture was stirred at -78°C for 0.5 hours. Then tetrahydro-4Hpyran-4-one (45 mg, 0.45 mmol) was added to the mixture. The mixture was stirred at -78°C for 2 hours. The mixture was quenched with saturated aqueous NH4CI (2 mL). The mixture
The residue was purified by silica gel chromatography (petroleum ethenethyl acetate=1:1) to give N-((3-methoxy-5-methylpyrazin-2-yl)methyl)tetrahydro-2H-pyran-2-carboxamide (250 mg, 72% yield). LC-MS: tR - 0.70 min (method 2), m/z = 266.2 [M + Hf.
Step 2: To a solution of /V-((3-methoxy-5-methylpyrazin-2-yl)methyl)tetrahydro-2/-/-pyran-2carboxamide (250 mg, 0.94 mmol) in dioxane (8 mL) was added POCI3 (480 mg, 3.13 mmol) The solution was stirred at 90°C for 2h The mixture was cooled and concentrated in vacuo. The residue was diluted with DCM (50 mL), washed with saturated aqueous NaHCO3 (aq) (50 mL) and brine (50 mL). The organic layer was dried over Na2SO4 and concentrated in vacuo to give 8-methoxy-6-methyl-3-(tetrahydro-2/-/-pyran-2-yl)imidazo[1,5a]pyrazine (200 mg, 86% yield).
Step 3: To a solution of 8-methoxy-6-methyl-3-(tetrahydro-2H-pyran-2-yl)imidazo[1,5a]pyrazine (270 mg, 1,09 mmol) in dioxane (8 mL) was added 2M HCI(aq) (4 mL). The solution was stirred at 90DC for 1 hour. The mixture was concentrated in vacuo and added saturated aqueous NaHCO3 (50 mL). The mixtue was extracted with DCM (50 mL x 2). The organic layer was washed with brine (50 mL) and concentrated in vacuo to give 6-methyl-3(tetrahydro-2/-/-pyran-2-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one (200 mg, 79% yield).
Step 4: To a solution of 6-methyl-3-(tetrahydro-2/-/-pyran-2-yl)imidazo[1,5-a]pyrazin-8(7H)one (200 mg, 0.86 mmol) in arihydrous DMF (10 mL) was added K2CO3 (237 mg, 1.71 mmol) and 1-(bromomethyl)-3-fluorobenzene (243 mg, 1.29 mmol). The mixture was stirred at 80°C for 24h. The mixture was cooled and diluted with water (100 mL), extracted with EtOAc (50 mL χ 3). The organic layer was washed with brine (50 mL), dried over Na2SO4 and concentrated in vacuo to give 7-(3-fluorobenzyl)-6-methyl-3-(tetrahydro-2H-pyran-2yl)imidazo[1l5-a]pyrazin-8(7H)-one (130 mg, 44% yield).
Step 5: 7-(3-fluorobenzyl)-6-methyl-3-(tetrahydro-2/7-pyran-2-yl)imidazo[1,5-a]pyrazin-8(7/-/)one (130 mg, 380.8 pmol) was purified by SFC.
7-(3-fluorobenzyl)-6-methyl-3-(tetrahydro-2H-pyran-2-yI)imidazo[1,5-a]pyrazin-8(7H)-one, stereoisomer 1 (35 mg, 27% yield) was obtained.
1H NMR (CDCl3 400 MHz): 57.91 (s, 1H), 7.32-7.28 (m, 1H), 7.19(s, 1H), 6.98-6.94 (m, 2H), 6.89 (d. J = 9.6 Hz, 1 H), 5.23 (s, 2H), 4.76 (t, J = 6.4 Hz, 1 H). 4.06 (d, J = 10.8 Hz. 1 H), 3.67 (t, J= 10.8 Hz, 1H), 2.23 (s, 3H), 2.17-2.05 (m, 3H), 1.74-1.68 (m, 3H),
LC-MS: tR = 2.33 min (method 3), m/z = 342.1 [M + H]+. SFC: tR = 5.478 min, ee% = 99.90%. [a]D20+16.00 (c = 0.10, CHCI3).
7-(3-fluorobenzyl)-6-methyl-3-(tetrahydro-2H-pyran-2-yl)imidazo[1,5-a]pyrazin-8(7H)-one, stereoisomer 2 (33 mg, yield: 35%) was obtained.
1H NMR (CDCI3 400 MHz): <5 7.92 (s, 1H), 7.32-7.28 (m, 1H), 7.19(s, 1H), 6.98-6.94 (m, 2H), 6.89 (d, J= 9.2 Hz, 1H), 5.23 (s, 2H), 4.77 (t, J = 6.8 Hz, 1H), 4.06 (d, J= 10.8 Hz, 1H), 3.67 (t, J = 10.8 Hz, 1H), 2.17 (s, 3H), 2.12-2.02 (m, 3H), 1.74-1.68 (m, 3H).
LC-MS. iR = 2.33 min (method 3), mlz = 342.1 [M + H]’. SFC: tR = 5.789 min, ee% = 98.92%. [a]D 20 -23.33 (c = 0.10, CHCI3).
Example 31:
o
7-(3-fluorobenzyl)-6-methyl-3-(tetrahydrofuran-3-yl)imidazo[1,5-a]pyrazin-8(7H)-one, stereosiomer 1 and 2:
Step 1: To a solution of (3-methoxy-5-methylpyrazin-2-yl)methanamine (200 mg, 1.3 mmol) in dry DCM (10 mL) was added tetrahydrofuran-3-carboxylic acid (228 mg, 2.0 mmol), Et3N (265 mg, 2.6 mmol) and HATU (747 mg, 2.0 mmol). The mixture was stirred at 15°C for 16 hours. Water (10 mL) was added to the mixture. The organic layer was washed with brine (10 mL), dried over Na2SO4, filtered and concentrated to give the crude product. The crude product was purified by flash chromatography on silica gel (10%~100% ethyl acetate in petroleum ether) to give A/-((3-methoxy-5-methylpyrazin-2-yl)methyl)tetrahydrofuran-3carboxamide (200 mg, 61% yield).
Step 2: To a solution of A/-((3-methoxy-5-methylpyrazin-2-yl)methyl)tetrahydrofuran-3carboxamide (300 mg, 1.19 mmol) in dioxane (5 mL) was added POCI3 (366 mg, 2.39 mmol). The mixture was heated at 90°C for 2 hours. The mixture was cooled to 15°C and adjusted to pH=8 by saturated aqueous NaHCO3. The aqueous layer was extracted with DCM (20 mL x 2). The combined organic layer was washed with H2O (20 ml), brine (20 mL), dried over Na2SO41 filtered and concentrated to give 8-methoxy-6-methyl-3-(tetrahydrofuran-
3-yl)imidazo[1,5-a]pyrazine (300 mg).
Step 3: To a solution of 8-methoxy-6-methyl-3-(tetrahydrofuran-3-yl)imidazo[1,5-a]pyrazine (300 mg, 1.29 mmol) in dioxane (5 mL) was added 2 N HCl (2 mL). The mixture was heated at 90°C for 1 hour. The mixture was cooled to 15°C and extracted with DCM (20 mL * 2). The combined organic layer was washed with H2O (20 mL), brine (20 mL), dried over Na2SO4, filtered and concentrated to give 6-methyl-3-(tetrahydrofuran-3-yl)imidazo[1,5a]pyrazin-8(7H)-one (210 mg, 74% yield).
Step 4: To a solution of 6-methyl-3-(tetrahydrofuran-3-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one (200 mg, 912.24 pmol) in dry DMF (5 mL) was added 1-(bromomethyl)-3-fluorobenzene (259 mg, 1.37 mmol) and K2CO3 (252 mg, 1.82 mmol). The mixture was stirred at 60°C for 16 hours. The mixture was concentrated and the residue was dissoived in DCM (20 mL) and H2O (10 mL). The aqueous layer was extracted with DCM (20 mL * 2). The combined organic layer was washed with H2O (20 mL), brine (20 mL), dried over Na2SO41 filtered and concentrated to give the crude product. The crude product was purified by flash chromatography on silica gel (10%~100% ethyl acetate in petroleum ether) to give 7-(3fluorobenzyl)-6-methyl-3-(tetrahydrofuran-3-yl)imidazo[1r5-a]pyrazin-8(7/-/)-one (40 mg, 13% yield).
Step 5: 7-(3-fluorobenzyl)-6-methyl-3-(tetrahydrofuran-3-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one « (40 mg, 122.2 pmol) was purified by SFC to give 7-(3-fluorobenzyl)-6-methyl-3(tetrahydrofuran-3-yl)imidazo[1,5-a]pyrazin-8(7H)-one, stereoisomer 1 (16.43 mg, 41% yield).
’H NMR (CDCI3 400 MHz): δ 7.90 (s, 1 H), 7.31 -7.28 (m. 1 H), 6.98-6.93 (m, 2H), 6.89 (d, J =
9.2 Hz, 1H), 6.79 (s, 1H), 5.21 (s, 2H), 4.19-4.17 (m, 1H), 4.12-4.09 (m, 1H), 4.05-3.95 (m, 2H), 3.66-3.62 (m, 1H), 2.40 (q, J= 7.2 Hz, 2H), 2.16 (s, 3H).
LC-MS: tR = 1.964 min (method 3), mlz = 328.0 [M + H]4. SFC: tR - 4.503 min, ee% =99.8%; [α]ο 20 +14.7 (c — 0.10, DCM).
7-(3-fluorobenzyl)-6-methyl-3-(tetrahydrofuran-3-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one, stereoisomer 2 (15.58 mg, 38% yield).
1H NMR (CDCI3 400 MHz): δ 7.90 (s, 1 H), 7.29-7.27 (m, 1 H), 6.98-6.92 (m, 2H), 6.89 (d, J =
9.6 Hz, 1H), 6.79 (s, 1H), 5.21 (s, 2H), 4.19 (t, J = 8.4 Hz, 1 H), 4.11-4.09 (m, 1H), 4.05-4.03 (m, 1H), 3.97-3.95 (m, 1H), 3.66-3.62 (m, 1H), 2.38 (q, J = 7.6 Hz, 2H), 2.16 (s, 3H).
LC-MS: tR = 1.957 min (method 3), m/z = 328.0 [M + H]4. SFC: tR = 4.779 min, ee% =96%; [α]0 20 -14.0 (c = 0.10, DCM).
Example 32:
T-fS-fluorobenzylJ-fi-methyl-S-tS-methyltetrahydrofuran-S-ylJimidazoIl.S-aJpyrazin8(7H)-one, stereoisomer 1 and 2:
Step 1: To a solution of (3-methoxy-5-methylpyrazin-2-yl)methanamine (200 mg, 1.3 mmol) in DCM (6 mL) was added 3-methyltetrahydrofuran-3-carboxylic acid (255 mg, 1.9 mmol) and HATU (894 mg, 2.4 mmol), Et3N (264 mg, 2.6 mmol). The solution was stirred at 2025°C for 1 hour. Water (40 ml) was added, the mixture was extracted with DCM (40 mL * 2). The organic layer was washed with brine (30 mL), dried over Na2SO4 and concentrated in vacuo. The residue was purified by silica gel chromatography(petroleum ethenethyl acetale=1:1) to give A/-((3-methoxy-5-methylpyrazin-2-yl)methyl)-3-methyltetrahydrofuran-3carboxamide (300 mg, 67% yield, 78% purity).
Step 2: To a solution of A/-((3-methoxy-5-methylpyrazin-2-yl)methyl)-3methyltetrahydrofuran-3-carboxamide (400 mg, 1.5 mmol) in dioxane (6 mL) was added POCI3 (880 mg, 5.7 mmol). The solution was stirred at 80-90’C for 2h. The mixture was cooled and concentrated in vacuo. The residue was diluted with DCM (50 mL), washed with saturated aqueous NaHCO3(50 mL) and brine (50 mL). The organic layer was dried over Na2SO4 and concentrated in vacuo to give 8-methoxy-6-methyl-3-(3-methyltetrahydrofuran3-yl)imidazo[1,5-a]pyrazine (350 mg, 94% yield).
Step 3: To a solution of 8-methoxy-6-methyl-3-(3-methyltetrahydrofuran-3-yl)imidazo[1,5a]pyrazine (300 mg, 1.2 mmol) in dioxane (8 mL) was added 2M HCI(aq) (4 mL). The solution was stirred at 80-90°C for 1 hour. The mixture was concentrated in vacuo and added saturated aqueous NaHCO3 (50 mL). The mixtue was extracted with DCM(50 mL * 2). The organic layer was washed with brine (20 mL) and concentrated in vacuo to give 6methyl-3-(3-methyltetrahydrofuran-3-yl)imidazo[1,5-a]pyrazin-8(7H)-one (260 mg, 92% yield).
Step 4: To a solution of 6-methyl-3-(3-methyltetrahydrofuran-3-yl)imidazo[1,5-a]pyrazin8(7H)-one (260 mg, 1.1 mmol) in anhydrous DMF (10 mL) was added K2CO3 (308 mg, 2.2 mmol) and 1-(bromomethyl)-3-fluorobenzene (316 mg, 1.7 mmol). The mixture was stirred at 70-80°C for 2h. The mixture was cooled and diluted with water (50 mL), extracted with EtOAc (50 mL x 2). The organic layer was washed with brine (20 mL), dried over Na2SO4 and concentrated in vacuo to give 7-(3-fluorobenzyl)-6-methyl-3-(3-methyltetrahydrofuran-3yl)imidazo[1,5-a]pyrazin-8(7/7)-one (160 mg, 42% yield).
Step 5: 7-(3-fluorobenzyl)-6-methyl-3-(3-methyltetrahydrofuran-3-yl)imidazo[1,5-a]pyrazin8(7H)-one (160 mg, 0.47 mmol) was separated by SFC to give 7-(3-fluorobenzyl)-6-methyl3-(3-methyltetrahydrofuran-3-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one, stereoisomer 1 (37 mg, 23% yield) as a off-white solid. 1H NMR (CDCI3400 MHz): 5 7.88 (s, 1H), 7.32-7.26 (m, 1H), 6.94-6.82 (m, 4H), 5.21 (s, 2H), 4.33 (d, J = 8.8 Hz, 1 H), 4.07-4.04 (m, 1 H), 4.00-3.98 (m, 1H), 3.87 (d, J = 8.8 Hz, 1H), 2.62-2.57 (m, 1H), 2.16 (s, 3H), 2.14-2.09 (m, 1H), 1.60 (s, 3H), . LC-MS: tR = 2.47 min (method 3), m/z = 342.1 [M + H]+. SFC: tR = 4.91 min, ee% > 99%. [a]D 20=ί-5.0 (c = 0.10, MeOH).
7-(3-fluorobenzyl)-6-methyl-3-(3-methyltetrahydrofuran-3-yl)imidazo[1,5-a]pyrazin-8(7H)one, stereoisomer 2 (44 mg, 27% yield) as a off-white solid.
Ή NMR (CDCI3400 MHz): 57.82 (s, 1H), 7.24-7.20 (m, 1H), 6.94-6.82 (m, 4H), 5.15 (s, 2H),
4.27 (d, J = 8.8 Hz, 1 H), 4.01 -3.99 (m, 1 H), 3.96-3.92 (m, 1 H), 3.81 (d, J = 8.8 Hz, 1 H), 2.572.51 (m, 1H), 2.10 (s, 3H), 2.09-2.04 (m, 1H), 1.54 (s, 3H).
LC-MS: tR = 2.47 min (method 3), m/z = 342.1 [M + Hf.
SFC: iR = 5.33 min, ee% > 99%. [a]D 2°=-3.0 (c = 0.10, MeOH).
Example 33:
o ’wiï?
7-(3-fluorobenzyl)-6-methyl-3-(1-methylcyclopropyl)imidazo[1,5-a]pyrazin-8{7H)-one:
Step 1 : To a solution of 1-methylcyclopropane-1-carboxylic acid (500 mg, 4.99 mmol) in DCM (2 mL) was added (COCI)2 (3.17 g, 24.95 mmol). The solution was stirred at40°C for
2h. The reaction mixture was concentrated in vacuo to give 1-methylcyclopropane-1carbonyl chloride (500 mg, 85% yield).
Step 2: A solution of (3-methoxy-5-methylpyrazin-2-yl)methanamine (100 mg, 0.65 mmol) in anhydrous DCM (3 mL) was cooled to 0°C. Then a solution of 1-methylcyclopropane-1carbonyl chloride (100 mg, 0.85 mmol) in anhydous DCM (2 mL) was added dropwise and stirred at 0°C for 15 min. The mixture was diluted with DCM (20 mL), washed with saturated aqueous NaHCO3 (20 mL), brine (20 mL) and dried over Na2SO4. The organic layer was concentrated in vacuo to give A/-((3-methoxy-5-methylpyrazin-2-yl)methyl)-1methylcyclopropane-1-carboxamide (120 mg, 78% yield).
LC-MS: tR = 0.66 min (method 2), m/z = 236.1 [M + H]+.
Step 3: To a solution of N-((3-methoxy-5-methylpyrazin-2-yl)methyl)-1-methylcyclopropane1-carboxamide (120 mg, 0.51 mmol) in dioxane (5 mL) was added POCl3(590 mg, 3.85 mmol). The solution was stirred at 80-90°C for 2h. The mixture was cooled and slowly added into water (50 mL), extracted with EtOAc (30 mL * 2). The organic layer was washed with brine (20 mL), dried over Na2SO4 and concentrated in vacuo to give 8-methoxy-6-methyl-3(1-methylcyc!opropyl)imidazo[1,5-a]pyrazine (80 mg, 72% yield).
Step 4: To a solution of 8-methoxy-6-methyl-3-(1-methyicyclopropyl)imidazo[1,5-a]pyrazine (80 mg, 0.37 mmol) in dioxane (5 mL) was added 2M HCl (aq) (2 mL). The solution was stirred at 80-90°C for 1 hour. The mixture was concentrated in vacuo and added saturated aqueous NaHCO3 (50 mL). The mixtue was extracted with DCM (50 mL * 2). The organic layer was washed with brine (20 mL) and concentated in vacuo to give 6-methyl-3-(1methylcyclopropyl)imidazo[1,5-a]pyrazin-8(7/-/)-one (70 mg, 94% yield).
Step 5: To a solution of 6-methyl-3-(1-methylcyclopropyl)imidazo[1,5-a]pyrazin-8(7H)-one (70 mg, 0.34 mmol) in anhydrous DMF (4 mL) was added 1-(bromomethyl)-3-fluoro-benzene (98 mg, 0.52 mmol) and K2CO3 (95 mg, 0.69 mmol). The mixture was stirred at 70-80°C for 1 hour. The mixture was cooled and filtered. The filtrate was purified by preparative LC-MS to give 7-(3-fluorobenzyl)-6-methyl-3-(1-methylcyclopropyl)imidazo[1,5-a]pyrazin-8(7/-/)-one (35 mg, 32% yield).
1H NMR (CDCI3400 MHz): 5 7.84 (s, 1H), 7.33-7.39 (m, 1H), 7.01-6.89 (m, 4H), 5.23 (s, 2H), 2.20 (s, 3H), 1.60 (s, 3H), 1.11-1.09 (m, 2H), 0.88-0.85 (m, 2H).
LC-MS: tR = 2.34 min (method 3), mlz = 312.1 [M + H]+.
Example 34:
ο
3-(2,2-difluorocyclopropyl)-7-(3-fluorobenzyl)-6-methylimidazo[1,5-a]pyrazin-8(7H)one:
Step 1: To a solution of (3-methoxy-5-methylpyrazin-2-yl)methanamine (100 mg, 0.65 mmol) in DCM (5 mL) was added 2,2-difluorocyclopropane-1-carboxylic acid (120 mg, 0.98 mmol) and HATU (447 mg, 1.18 mmol), Et3N (132 mg, 1.31 mmol). The solution was stirred at2025°C for 1 hour. The mixture was diluted with water (20 mL), extracted with DCM (30 mL * 2). The organic layer was washed with brine (20 mL), dried over Na2SO4 and concentrated in vacuo. The residue was purified by silica gel chromatography(petroleum ether:ethyl acetate=1:1) to give 2,2-difluoro-A/-((3-methoxy-5-methylpyrazin-2-yl)methyl)cyclopropane-1carboxamide (200 mg, 89% yieid, 75% purity).
Step 2. To a solution of 2.2-difluoro-N-((3-methoxy-5-methy!pyrazin-2yl)methyl)cyclopropane-1-carboxamide (200 mg, 0.58 mmol, 75% purity) in dioxane (5 mL) was added POCI3 (1.12 g, 7.3 mmol). The solution was stirred at 90°C for 2h. The mixture was cooled and concentrated in vacuo. The residue was diluted with DCM (50 mL), washed with saturated aqueous NaHCO3(aq) (50 mL) and brine (50 mL). The organic layer was dried over Na2SO4 and concentrated in vacuo to give 3-(2,2-difluorocyclopropyl)-8-methoxy-6methylimidazo[1,5-a]pyrazine (120 mg, 86% yieid).
Step 3: To a solution of 3-(2,2-difluorocyclopropyl)-8-methoxy-6-methylîmidazo[1,5a]pyrazine (120 mg, 0.50 mmol) in dioxane (5 mL) was added 2M HCI(aq) (3 mL). The solution was stirred at 80°C for 1 hour. The mixture was concentrated in vacuo and added saturated aqueous NaHCO3 (50 mL). The mixtue was extracted with DCM (50 mL x 2). The organic layer was washed with brine (20 mL) and concentated in vacuo to give 3-(2,2difluorocyclopropyl)-6-methylimidazo[1,5-a]pyrazin-8(7H)-one (100 mg, 89% yieid).
LC-MS: fR = 0.94 min (method 10), m/z = 226.2 [M + H]+.
Step 4: To a solution of 3-(2,2-difluorocyclopropyl)-6-methylimidazo[1,5-a]pyrazin-8(7H)-one (100 mg, 0.44 mmol) in anhydrous DMF (5 mL) was added K2CO3 (123 mg, 0.89 mmol) and 1-(bromomethyl)-3-fluorobenzene (126 mg, 0.67 mmol). The mixture was stirred at 80°C for
2h. The mixture was cooled and filtered. The filtrate was purified by preparative LC-MS to give 3-(2,2-difluorocyclopropyl)-7-(3-fluorobenzyl)-6-methylimidazo[1,5-a]pyrazin-8(7H)-one (40 mg, 27% yield) as a whtie solid.
1H NMR (CDCI3400 MHz): 07.90 (s, 1H), 7.30-7.28 (m, 1H), 6.98-6.84 (m, 4H), 5.28-5.16 (m, 2H), 2.80-2.73 (m, 1H), 2.38-2.37 (m, 1H), 2.19 (s, 3H), 2.05-2.04 (m, 1H).
LC-MS: = 2.67 min (method 3), m/z = 334.1 [M + H]*
Example 35:
o
7-(3-fluorobenzyl)-6-methyl-3-(2-methyIcyclopropyl)imidazo[1,5-a]pyrazin-8(7H)-one, stereoisomer 1, 2, 3 and 4:
Step 1: To a solution of (3-methoxy-5-methylpyrazin-2-yl)methanamine (100 mg, 652.8 pmol) and 2-methyicyclopropane-1-carboxylic acid (98 mg, 979.2 pmol) in DCM (5 mL) was added HATU (446.8 mg, 1.2 mmol) and trîethylamine (132.1 mg, 1.3 mmol). The mixture was stirred at 24°C for 16h. The mixture was diluted with DCM (20 mL) and washed with water (15 mL). The aqueous layer was extracted with DCM (2*30 mL). The combined organic layer was washed with brine (20 mL), dried over Na2SO4, filtered and concentrated. The residue was purified by preparative TLC (ethyl acetate) to give A/-((3-methoxy-5methylpyrazin-2-yl)methyl)-2-methylcyclopropane-1-carboxamide (150 mg, 95% yield).
Step 2: To a solution of A/-((3-methoxy-5-methylpyrazin-2-yl)methyl)-2-methylcyclopropane1-carboxamide (150 mg, 636 pmol) in dioxane (5 mL) was added POCI3 (400 mg, 2.6 mmol). The mixture was stirred at 90°C for 2h. The mixture was cooled down to 25°C, neutralized with saturated aqueousNaHCO3 and extracted with ethyl acetate (3 * 30 mL). The combined organic layer was washed with brine (30 mL), dried over Na2SO4, filtered and concentrated to give the crude 8-methoxy-6-methyl-3-(2-methylcyclopropyl)imidazo[1,5a]pyrazine (130 mg, 94% yield). This crude product was used directly for the next step.
Step 3: A solution of 8-methoxy-6-methyl-3-(2-methylcyclopropyl)imidazo[1,5-a]pyrazine (120 mg, 552.3 pmol) in dioxane (5 mL) and HCl (2 M, 2 mL) was stirred at 80°C for 1 hour. The mixture was cooled to 25°C, neutralized with saturated aqueous NaHCO3 and extracted with ethyl acetate (3 * 20 mL). The combined organic layerwas washed with brine (20 mL), dried over Na2SO4, filtered and concentrated to give the crude 6-methyl-3-(2methylcyclopropyl)imidazo[1,5-a]pyrazin-8(7/7)-one (100 mg, 89% yield). This crude product was used directiy for the next step.
Step 4: To a solution of 6-methyl-3-(2-methylcyclopropyl)imidazo[1,5-a]pyrazin-8(7/-/)-one (100 mg. 492.0 pmol) and 1-(bromomethyl)-3-fluorobenzene (139.5 mg, 738.0 pmol) in DMF (5 mL) was added K2CO3 (136 mg, 984 pmol). The mixture was stirred at 60-70°C for 16h. The mixture was cooled to 25°C, diluted with water (15 mL), extracted with ethyl acetate (3 * 30 mL). The combined organic layer was washed with brine (30 mL), dried over Na2SO4, filtered and concentrated. The residue was purified by column chromatography on silica gel (eluent of 0%~50% ethyl acetate in petroleum ether) to give 7-(3-fluorobenzyl)-6methyl-3-(2-methylcyclopropyl)imidazo[1,5-a]pyrazin-8(7/7)-one (80 mg, 52% yield).
Step 5: 7-(3-fluorobenzyl)-6-methyl-3-(2-methylcyclopropyl)imidazo[1,5-a]pyrazin-8(7H)-one (100 mg, 321.2 pmol) was purified by SFC.
7-(3-fluorobenzyl)-6-methyl-3-(2-methylcyclopropyl)imidazo[1,5-a]pyrazin-8(7/7)-one1 stereoisomer 1 (35 mg, 27% yield) was obtained.
’H NMR (CDCI3 400 MHz): δ 7.83 (s, 1H), 7.33-7.29 (m, 1H), 7.00-6.94(m, 2H), 6.91-6.89 (m, 2H). 5.23 (s, 2H), 2.19 (s, 3H), 1.59-1.55 (m, 1H), 1.54-1.50 (m, 1H), 1.35-1.30 (m, 1H),
1.27 (d, J= 6.0 Hz, 3H), 0.89-0.88 (m, 1H).
LC-MS: tR = 2.03 min (method 3), m/z = 312.1 [M + H]+. SFC: tR = 4.466 min, ee% > 99%. [a]D20 +29.3 (c = 0.10, CHCI3).
7-(3-fluorobenzyl)-6-methyl-3-(2-methylcyclopropyl)imidazo[1,5-a]pyrazin-8(7H)-one, stereoisomer 2 (26 mg, 26% yield) was obtained.
1H NMR (CDCI3 400 MHz): δ 7.84 (s, 1 H), 7.32-7.29 (m, 1 H), 7.00-6.96(m, 2H), 6.90-6.89 (m, 2H), 5.23 (s, 2H), 2.19 (s, 3H), 1.62-1.60 (m, 1H), 1.55-1.53 (m, 1H), 1.36-1.34 (m, 1H),
1.27 (d, J= 5.6 Hz, 3H), 0.91-0.89 (m, 1H).
LC-MS: tR = 2.02 min (method 3), mlz = 312.1 [M + H]+. SFC: tR = 5.227 min, ee% > 99%. [a]D20-15.0 (c = 0.10, CHCI3).
7-(3-fluorobenzyl)-6-methyl-3-(2-methylcyclopropyl)imidazo[1,5-a]pyrazin-8(7/7)-one, stereoisomer 3 (8.0 mg, 8% yield) was obtained.
1H NMR (CDCI3 400 MHz): <5 7.89 (s, 1H), 7.33-7.30 (m, 1H), 7.01-6.91 (m, 4H), 5.29 (d, J= 16.0 Hz, 1H), 5.17 (d, J= 16.0 Hz, 1H). 2.19 (s, 3H), 2.01-1.97(m, 1H), 1.39-1.27 (m. 1H), 1.23-1.20 (m, 2H), 0.91 (d, J= 6.0 Hz, 3H).
LC-MS: tR = 1.98 min (method 3), mlz = 312.1 [M + H]+. SFC: tR = 6.995 min, ee% > 99%. [a]D20 +37.0 (c = 0.10, CHCI3).
7-(3-fluorobenzyl)-6-methyl-3-(2-methylcyclopropyl)imidazo[1,5-a]pyrazin-8(7H)-one, stereoisomer 4 (9.0 mg. 9% yield) was obtained.
1H NMR (CDCI3 400 MHz): <5 7.86 (s, 1 H), 7.29-7.26 (m, 1 H), 6.99-6.88(m, 4H), 5.27 (d, J= 16.0 Hz, 1H), 5.15 (d, J= 16.0 Hz, 1H), 2.17 (s, 3H), 1.97-1.95(m, 1 H), 1.58-1.53 (m, 1H), 1.23-1.20 (m, 2H), 0.91 (d, > 6.0 Hz, 3H).
LC-MS: fR = 1.98 min (method 3), mlz = 312.1 [M + H]+. SFC: tR = 8.704 min, ee% > 99%. [a]D20 -66.7 (c = 0.10, CHCI3).
Example 36:
7-(3-fluorobenzyl)-6-methyl-3-(2-methyltetrahydrofuran-3-yl)imidazo[1,5-a]pyrazin8(7H)-one, stereoisomer 1,2, 3 and 4:
Step 1: To a solution of (3-methoxy-5-methylpyrazin-2-yl)methanamine (300 mg, 2.0 mmol), 2-methyltetrahydrofuran-3-carboxylic acid (382 mg, 2.9 mmol) in DCM (10 mL) was added HATU (1.3 g, 3.5 mmol) and triethylamine (396 mg, 3.9 mmol). The mixture was stirred at 24°C for 16h. The mixture was diluted with DCM (30 mL) and washed with water (20 mL). The aqueous layer was extracted with DCM (2 * 30 mL). The combined organic layer was washed with brine (30 mL), dried over Na2SO4, filtered and concentrated. The residue was purified by column chromatography on silica gel (0%~70% ethyl acetate in petroleum ether) to give A/-((3-methoxy-5-methylpyrazin-2-yl)methyl)-2-methyltetrahydrofuran-3-carboxamide (350 mg, 62% yield).
Step 2: To a solution of A/-((3-methoxy-5-methylpyrazin-2-yl)methyl)-2methyltetrahydrofuran-3-carboxamide (350 mg, 1.3 mmol) in dioxane (5 mL) was added
POCI3 (720 mg, 4.7 mmol). The mixture was stirred at 90°C for 2h. The mixture was cooled to 25°C, neutralized with saturated aq.NaHCO3 and extracted with ethyl acetate (2 * 30 mL). The combined organic layer was washed with brine (20 mL), dried over Na2SO4, filtered and concentrated to give crude 8-methoxy-6-methyl-3-(2-methyltetrahydrofuran-3-yl)imidazo[1,5a]pyrazine (320 mg). The crude was used directly for the next step.
Step 3: A solution of 8-methoxy-6-methyl-3-(2-methyltetrahydrofuran-3-yl)imidazo[1.5a]pyrazine (320 mg, 1.3 mmol) in dioxane (5 mL) and HCl (2 M, 2 mL) was stirred at 80°COO’C for 21.5 hours. The mixture was cooled down to 25°C, neutralized with saturated aq.NaHCO3, extracted with DCM (3 χ 30 mL). The combined organic layer was washed with brine (30 mL), dried over Na2SO4, filtered and concentrated to give crude 6-methyl-3-(2methyltetrahydrofuran-3-yl)imidazo[1,5-a]pyrazin-8(7H)-one (300 mg). The crude product was used directly for the next step.
Step 4: To a solution of 6-methyl-3-(2-methyltetrahydrofuran-3-yl)imidazo[1,5-a]pyrazin8(7H)-one (250 mg, 1.1 mmol) in DMF (8 mL) was added 1-(bromomethyl)-3-fluorobenzene (304 mg, 1.6 mmol) and K2CO3 (296 mg, 2.1 mmol). The mixture was stirred at 60-70°C for 16h. The mixture was cooled down to 25°C and diluted with water (15 mL), extracted with ethyl acetate (3 χ 30 mL). The combined organic layer was washed with brine (30 mL), dried over Na2SO4, filtered and concentrated. The residue was purified by column chromatography on silica gel (eluent of 0%~30% ethyl acetate in petroleum ether) to give 7-(3-fluorobenzyl)-
6- methyl-3-(2-methyltetrahydrofuran-3-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one (170 mg, 47% yield).
Step 5: 7-(3-fluorobenzyl)-6-methyl-3-(2-methyltetrahydrofuran-3-yl)imidazo[1,5-a]pyrazin8(7H)-one (220 mg, 644 pmol) was purified by SFC.
7- (3-fluorobenzyl)-6-methyl-3-(2-methyltetrahydrofuran-3-yl)imidazo[1,5-a]pyrazin-8(7/-/)one, stereoisomer 1 (20 mg, 9% yield).
'H NMR (CDCI3400 MHz400 MHz): 5 7.95 (s, 1H), 7.34-7.28 (m, 1H), 7.01-6.89 (m, 3H), 6.79 (s, 1H), 5.23 (s. 2H), 4.35-4.30 (m, 1H), 4.13-4.07 (m, 2H), 3.12-3.06 (m, 1H), 2.50-2.37 (m, 2H), 2.19 (s, 3H), 1.35 (d, J= 6.0 Hz, 3H.
LC-MS: tR = 2.12 min (method 3), mlz = 342.1 [M + Hf.
SFC: tR = 4.812 min, ee% > 99%. [a]D 20 -24.3 (c = 0.10, CHCI3).
7-(3-fluorobenzyl)-6-methyl-3-(2-methyltetrahydrofuran-3-yl)imidazo[1,5-a]pyrazin-8(7/-/)one, stereoisomer 2 (10 mg, 5% yield).
'H NMR (CDCI3 400 MHz): 5 7.93 (s, 1 H), 7.31-7.26 (m, 1H), 6.99-6.87 (m, 3H), 6.76 (s, 1H), 5.21 (s, 2H), 4.32-4.27 (m, 1H), 4.10-4.04 (m, 2H). 3.10-3.03 (m, 1H), 2.48-2.35 (m, 2H), 2.17 (s, 3H), 1.33 (d, J= 6.4 Hz, 3H).
LC-MS: tR = 2.07 min (method 3), mlz = 342.1 [M + H]*.
SFC: tR = 5.088 min. ee% = 97.9%. [a]D 20 +10.3 (c = 0.10, CHCI3).
7-(3-fluorobenzyl)-6-methyl-3-(2-methyltetrahydrofuran-3-yl)imidazo[1,5-a]pyrazin-8(7/-/)one, stereoisomer 3 (38.0 mg, 17% yield) .
'H NMR (CDCI3 400 MHz): 5 7.95 (s, 1H), 7.31-7.29 (m, 1H), 7.01-6.89 (m, 3H), 6.83 (s, 1H), 5.29 (d, J= 16.4 Hz, 1H), 5.17 (d, J= 16.4 Hz, 1H), 4.35-4.28 (m, 2H), 3.91-3.87 (m. 1H), 3.71-3.67 (m, 1H), 2.72-2.67 (m, 1H), 2.44-2.40 (m, 1H), 2.18 (s, 3H), 0.90 (d, J= 6.4 Hz, 3H).
LC-MS: tR = 2.02 min (method 3), mlz = 342.1 [M + H]+. SFC: tR = 5.516 min, ee% > 99%. [a]D20 +46.3 (c — 0.10, CHCI3).
7-(3-fluorobenzyl)-6-methyl-3-(2-methyltetrahydrofuran-3-yl)imidazo[1,5-a]pyrazin-8(7/-/)one, stereoisomer 4 (30.0 mg, 14% yield). 1H NMR (CDCI3 400 MHz): 5 7.95 (s, 1H), 7.337.30 (m, 1H), 7.01-6.90 (m, 3H), 6.83 (s, 1H), 5.29 (d, J= 16.4 Hz, 1H), 5.17 (d, J= 16.4 Hz, 1H), 4.37-4.28 (m, 2H), 3.91-3.87 (m, 1H), 3.71-3.69 (m, 1H), 2.72-2.68 (m, 1H), 2.45-2.40 (m, 1H), 2.18 (s, 3H), 0.90 (d, J= 6.8 Hz, 3H).
LC-MS: tR = 1.98 min (method 3), mlz - 342.1 [M + H]*. SFC: tR = 6.304 min, ee% > 99%. [a]D 20-47.0 (c = 0.10, CHCI3).
Example 37:
OOÔQ·
7-(3-fluorobenzyl)-3-(c/s-2-fluorocyclopropyl)-6-methylimidazo[1,5-a]pyrazin-8(7H)one, stereoisomer 1 and 2:
Step 1: A solution of (3-methoxy-5-methylpyrazin-2-yl)methanamine hydrochloride (400 mg, 2.1 mmol) and triethylamine (662 mg, 6.5 mmol) in DCM (8 mL) was cooled to 0°C, 218771 fluorocyclopropane-1-carbonyl chloride (251 mg, 2.1 mmol) was added dropwise and the mixture was stirred at 0°C for 0.5h. The mixture was diluted with water (10 mL), extracted with DCM (20 mL χ 2). The organic layer was washed with brine (20 mL), dried over Na2SO4 and concentrated in vauco. The residue was purified by préparative TLC (petroleum etherethyl acetate=1:1) to give c/s-2-fluoro-A/-((3-methoxy-5-methylpyrazin-2yl)methyl)cyclopropane-1-carboxamide (200 mg. 40% yield) and (1S,2/?)-2-fluoro-/V-((3methoxy-5-methylpyrazin-2-yl)methyl)cyclopropane-1-carboxamide (200 mg, 40% yield) ail.
Step 2: To a solution of c/s-2-fluoro-A/-((3-methoxy-5-methylpyrazin-2yl)methyl)cyclopropane-1-carboxamide (260 mg, 1.1 mmol) in dioxane (10 mL) was added POCI3 (500 mg, 3.3 mmol). The solution was stirred at 80-90°C for 2h. The mixture was concentrated in vacuo and diluted with NaHCO3 (30 mL), extracted with DCM (50 mL χ 2). The organic layer was washed with brine (30 mL), dried over Na2SO4 and concentrated in vacuo to give 3-(c/s-2-f!uorocyclopropyl)-8-methoxy-6-methylimidazo[1,5-a]pyrazine (220 mg, 91% yield).
Step 3: A solution of 3-(c/s-2-fluorocyclopropyl)-8-methoxy-6-methylimidazo[1,5-a]pyrazine (220 mg, 994 pmol) in 2N HCl (aq) (5 mL) and dioxane (10 mL) was stirred at 80-90°C for 1 .1 hour. The mixture was concentrated in vacuo. The residue was diluted with NaHCO3(aq) (30 mL), extracted with DCM (30 mL χ 3). The organic layer was washed with brine (30 mL), dried over Na2SO4 and concentrated in vacuo to give 3-(c/s-2-fluorocyclopropyl)-6methylimidazo[1,5-a]pyrazin-8(7H)-one (200 mg, 97% yield).
Step 4: To a solution of 3-(c/s-2-fluorocyclopropyl)-6-methylimidazo[1l5-a]pyrazin-8(7H)-one (200 mg, 965 pmol) in anhydrous DMF (10 mL) was added K2CO3 (133 mg, 965 pmol) and 1-(bromomethyl)-3-fluorobenzene (274 mg, 1.5 mmol). The mixture was stirred at 60-70°C for 16h and 80°C for 21 h. The mixture was cooled and filtered and he filtrate was purified by préparative LC-MS to give 7-(3-fluorobenzyl)-3-(c/s-2-fluorocyclopropyl)-6methylimidazo[1,5-a]pyrazin-8(7H)-one (80 mg, 26% yield).
Step 5: 7-(3-fluorobenzyl)-3-(c/s-2-fluorocyclopropyl)-6-methylimidazo[1,5-a]pyrazin-8(7H)one (80 mg. 253 pmol) was separated by SFC.
7-(3-fluorobenzyl)-3-(c/s-2-fluorocyc!opropyl)-6-methylimidazo[1,5-a]pyrazin-8(7/-/)-one, stereoisomer 1 (25 mg, 30% yield).
1H NMR (CDCI3 Varian_H_400 MHz): 5 7.92 (s. 1H), 7.32-7.26 (m, 1H), 7.00-6.88 (m, 4H), 5.29-5.15 (m, 2H), 5.02-4.84 (m, 1H), 2.18 (s, 3H), 2.12-1.99 (m, 2H), 1.44-1.25 (m. 1H).
LC-MS: = 2.00 min (method 8), mlz = 316.1 [M + Hf. SFC: Îr = 6.53 min, ee% > 99%. [a]D 20 -84.00 (c = 0.10, MeOH).
7-(3-fluorobenzyl)-3-(c/s-2-fluorocyclopropyl)-6-methyiimidazo[1,5-a]pyrazin-8(7H)-one, stereoisomer 2 (15 mg, 18% yield). 1H NMR (CDCI3 Varîan_H_400 MHz): 5 7.93 (s, 1H), 7.33-7.30 (m, 1H), 7.00-6.90 (m, 4H), 5.31-5.17 (m, 2H), 5.04-4.86 (m. 1 H), 2.20 (s, 3H),
12-2.00 (m. 2H). 1.46-1 42 (m. 1H).
LC-MS: iR = 1 99 min (method 8). mlz = 316.1 [M + Hf. SFC: tR = 5.06 min, ee% > 99%. [a]D 20 +75.00 (c = 0.10, MeOH).
Example 38:
L>··^
7-(3-fluorobenzyl)-3-(frans-2-fluorocyclopropyl)-6-methylimîdazo[1,5-a]pyrazin-8(7H)one, stereoisomer 1 and 2:
Step 1 : To a solution of frans-2-f[uoro-A/-((3-methoxy-5-methylpyrazin-2yl)methy[)cyclopropane-1-carboxamide (280 mg, 1.1 mmol) in dioxane (10 mL) was added POCI3 (540 mg, 3.5 mmol). The solution was stirred at 80-90°C for 2h. The mixture was concentrated in vacuo and diluted with NaHCO3 (30 mL), extracted with DCM (50 mL χ 2). The organic layer was washed with brine (30 mL), dried over Na2SO4 and concentrated in vacuo to give S-itrans^-fluorocyclopropyO-S-methoxy-e-methylimidazoEI.S-aJpyrazine (240 mg, 93% yield).
Step 2: A solution of 3-(frans-2-fluorocyclopropyl)-8-methoxy-6-methylimidazo[1,5-a]pyrazine (240 mg, 1.1 mmol) in 2N HCl (aq) (5 mL) and dioxane (10 mL) was stirred at 80-90°C for 1 hour. The mixture was concentrated in vacuo. The residue was diluted with NaHCO3(aq) (30 mL), extracted with DCM (30 mL χ 3). The organic layer was washed with brine (30 mL), dried over Na2SO4 and concentrated in vacuo to give 3-(frans-2-fluorocyclopropyl)-6methylimidazo[1,5-a]pyrazin-8(7H)-one (220 mg, 98% yield).
Step 3: To a solution of 3-(frans-2-fluorocyclopropyl)-6-methylimidazo[1,5-a]pyrazin-8(7H)one (220 mg, 1.1 mmol) in anhydrous DMF (10 mL) was added K2CO3 (293 mg, 2.1 mmol) and 1-(bromomethyl)-3-fluorobenzene (300 mg, 1.6 mmol). The mixture was stirred at 6070°C for 16h and 80°C for 21 h. The mixture was cooled and filtered and the filtrate was purified by préparative LC-MS to give 7-(3-fluorobenzyl)-3-(trans-2-fluorocyclopropyl)-6methylimidazo[1,5-a]pyrazin-8(7H)-one (250 mg, 77% yield).
Step 4: 7-(3-fluorobenzyl)-3-(trans-2-fluorocyclopropyl)-6-methylimidazo[1,5-a]pyrazin-8(7/-/)one (250 mg, 793 pmol) was separated by SFC
7-(3-fluorobenzyl)-3-(frans-2-fluorocyclopropyl)-6-methylimidazo[1,5-a]pyrazin-8(7H)-one. stereoisomer 1 (15 mg, 17% yield).
H NMR (CDCI3 400 MHz): 5 7.81 (s, 1H), 7.31-7.27 (m, 1H), 6.98-6.86 (m, 4H), 5.22 (s, 2H), 5.01-4.84 (m, 1H), 2.43-2.38 (m, 1H), 2.19 (s, 3H), 1.72-1.65 (m, 1 H), 1.58-1.55 (m, 1H).
LC-MS: tR = 2.24 min (method 8), m/z = 316.1 [M + H]*. SFC: tB = 2.83 min, ee% > 99%. [ajo20 +29.00 (c = 0.10, MeOH).
7-(3-fluorobenzyl)-3-(trans-2-fluorocyc1opropyl)-6-methylimidazo[1,5-a]pyrazin-8(7H)-one, stereoisomer 2 (45 mg, 17% yield).
1H NMR (CDCI3 400 MHz): 5 7.81 (s. 1H), 7.29-7.28 (m, 1H), 6.98-6.86 (m, 4H), 5.22 (s, 2H), 5.01-4.84 (m, 1H), 2.45-2.38 (m, 1H), 2.19 (s, 3H), 1.71-1.64 (m, 1H), 1.59-1.54 (m, 1H).
LC-MS: tR = 2.23 min (method 8), m/z = 316.1 [M + H]'. SFC: tR = 3.69 min, ee% > 99%. [a]D Z0-31 (c — 0.10, MeOH).
Example 39:
7-(4-cyclopropoxybenzyi)-6-methyl-3-(tetrahydro-2H-pyran-4-yl)îmidazo[1,5-a]pyrazin8{7H)-one:
Step 1: A solution of 1-bromo-4-cyclopropoxybenzene (900 mg, 4.22 mmol) in THF (20 mL, anhydrous) was added n-BuLi (2.5 M, 2.6 mL) at -78°C and stirred at -78°C for 2 hours under N2. Then, thereto was added dropwise DMF (926 mg, 12.66 mmol, anhydrous) at 78°C and it was stirred for 2 hours. The solution was quenched with NH4CI (aq. 1mL) at 78°C and stirred at 0°C for 0.5 hour. The mixture was diluted with ethyl acetate (10 mL). The mixture was filtered and the filtrate was concentrated under vacuum. The residue was diluted with ethyl acetate (30 mL), washed with brine (3*15 mL). The organic layer was dried with anhydrous Na2SO4, filtered and concentrated in vacuum to give 4cyclopropoxybenzaldehyde (700 mg). LC-MS: fR = 0.800 min (method 2), mlz = 162.8 [M + Hf.
Step 2: A solution of 4-cyclopropoxybenzaldehyde (700 mg) in MeOH (15 mL, anhydrous) was added NaBH4(319 mg, 8.44 mmol) at 0°C and stirred at 0°C for 1 hour. The solution was quenched with saturated aqueous NH4CI (aq. 0.5mL). The mixture was concentrated under vacuum. The residue was purified by silica gel chromatography petroleum ether/ethyl acetate=10/1, 1/1) to give (4-cyclopropoxyphenyl)methanol (540 mg, 78% yield).
Step 3: A solution of (4-cyclopropoxyphenyl)methanol (500 mg, 3.1 mmol) and Et3N (617 mg, 6.1 mmol) in anhydrous DCM (10 mL) was cooled to 0°C, then MsCI (1.41 g, 12.3 mmol) was added dropwise. The solution was stirred at 0°C for 0.5h. The mixture was diluted with water (50 mL), extracted with DCM (50 mL χ 2). The organic layer was washed with brine (30 mL), dried over Na2SO4 and concentrated in vacuo to afford 4cyclopropoxybenzyl methanesulfonate (600 mg, 81% yield).
Step 4: A mixture of 6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one (250 mg, 1.07 mmol), 4-cyclopropoxybenzyl methanesulfonate (311 mg, 1.28 mmol) and Cs2CO3 (698 mg, 2.14 mmol) in DMF (6.0 mL, anhydrous) was stirred at 60°C for 12 hours. The mixture was filtered and the filtrate was concentrated under vacuum. The residue was purified by silica gel chromatography (petroleum ether/ethyl acetate=10/1,0/1) to give 7-(4cyclopropoxybenzyl)-6-methyl-3-(tetrahydro-2/-/-pyran-4-yl)innidazo[1,5-a]pyrazin-8(7H)-one (320 mg, 77% yield).
1H NMR (CDCI3, 400 MHz): 5 7.92 (s, 1H), 7.15 (d. J = 8.8 Hz, 2H), 6.99 (d, J = 8.8 Hz, 2H),
6.73 (s, 1H) 5 17 (s, 2H), 4.12 (d, J = 10.4 Hz, 2H), 3.71 -3.69 (m, 1H), 3.67 -3.55 (m, 2H), 3.09 - 3.07 (m, 1H), 2.21 (s, 3H), 2.18 - 2.03 (m, 2H), 1.88 (d, J = 13.2 Hz, 2H), 0.79 - 0.71 (m, 4H).
LC-MS: iR = 2.154 min (method 3), m/z = 380.1 [M + H]+.
Example 40:
7-(4-(difluoromethoxy)benzyl)-6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5a]pyrazin-8(7W)-one
A mixture of 6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one (400 mg, 1.7 mmol), 1-(bromomethyl)-4-(difluoromethoxy)benzene (608 mg, 2.6 mmol), Cs2CO3 (1.11 g, 3.4 mmol) in DMF (50 mL) was stirred at 60 °C for 12 hours. The reaction mixture was concentrated. The residue was purified by silica gel chromatography (petroleum ether:ethyl acetate-5:1-0:1) to give 7-(4-(difluoromethoxy)benzyl)-6-methyl-3-(tetrahydro2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (360 mg, yield: 52%).
1H NMR(CDCI3, 400 MHz): 5 7.91 (s, 1H), 7.20 (d, J = 9.2 Hz, 2H), 7.07 (d, J =8.0 Hz, 2H),
6.73 (s, 1H), 6.46 (t, J- 73.6 Hz, 1H), 5.19 (s, 2H), 4.11 (d, J = 10.8 Hz, 2H), 3.56 (td, J = 12.0, 2.0 Hz, 2H), 3.10-3.04 (m, 1H), 2.17-2.06 (m, 5H), 1.86 (d, J= 13.2 Hz, 2H).
LC-MS: (r = 1.85 min (method 3), m/z = 390.1 [M + H]+.
Example 41:
O
6-methyl-3-(tetrahydro-2H-pyran-4-yl)-7-(4-(trifluoromethoxy)benzyl)imidazo[1,5a]pyrazin-8(7H)-one:
A mixture of 6-methyl-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one (400 mg, 1.7 mmol), 1-(bromomethyl)-4-(trifluoromethoxy)benzene (654 mg, 2.6 mmol) and
Cs2CO3 (1.11 g, 3.4 mmol) in DMF (50 mL) was stirred at 60 °C for 12h. The reaction mixture was concentrated. The residue was purified by silica gel chromatography (petroleum ether:ethyl acetate=5:1-0:1) to give 6-methyl-3-(tetrahydro-2H-pyran-4-yl)-7-(4(trifluoromethoxy)benzyl)imidazo[1,5-a]pyrazin-8(7/-/)-one (300 mg, yield: 41%).
nH NMR (CDCI3, 400 MHz): 5 7.91 (s, 1H), 7.25-7.22 (m, 2H), 7.17-7.15 (m, 2H), 6.74 (s, 1H). 5.21 (s. 2H). 4 11 (d. J = 10 4 Hz. 2H). 3.56 (td, J= 11.2, 2.0 Hz, 2H), 3.10 - 3 04 (m. 1H), 2.17 - 2.06 (m, 5H), 1.86 (d. J= 13.6 Hz, 2H).
LC-MS: fR = 2.05 min (method 3), mlz = 408.1 [M + H]*.
Example 42:
O
7-(4-(cyclopropylmethoxy)benzyl) -6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5a]pyrazin-8(7H)-one:
Step 1: A mixture of 4-hydroxybenzaldehyde (1.0 g, 8.19 mmol), (bromomethyl)cyclopropane 15 (1.33 g, 9.83 mmol) and K2CO3 (2.26 g, 16.38 mmol) in DMF (10.0 mL, anhydrous) was stirred at 20°C for 12 hours. The solution was diluted with water (20 mL). The aqueous phase was extracted with ethyl acetate (60 mL * 3). The combined organic phase was washed with brine (20 mL * 1), dried over anhydrous Na2SO4, filtered and concentrated in vacuum. The residue was purified by silica gel chromatography (petroleum ether/ethyl 20 acetate=10/1, 1/1) to give 4-(cyclopropylmethoxy)benzaldehyde (1.3 g, 87% yield).
Step 2: A solution of 4-(cyclopropylmethoxy)benzaldehyde (1.3 g, 7.4 mmol) in MeOH (30 mL) was cooied to 0°C, then NaBH4 (558 mg, 14.8 mmol) was added and the mixture was stirred at 0°C for 1 hour. The mixture was quenched with sat. brine (aq) (50 mL), extracted with EtOAc(50 mL χ 2). The organic layer was washed with brine, dried over Na2SO4 and 25 concentrated in vacuo to afford (4-(cyclopropylmethoxy)phenyl)methanol (1.21 g, 92% yield).
Step 3. A solution of (4-(cyclopropylmethoxy)phenyl)methanol (800 mg, 4.5 mmol)and Et3N (907 mg, 9-0 mmol) in DCM (10 mL) was cooied to 0cC, then MsCI (617 mg, 5.4 mmol) was added dropwise. The solution was stirred at 0°C for 0.5h. The mixture was diluted with water (50 mL), extracted with DCM (50 mL * 2). The organic layer was washed with brine (30 mL), dried over Na2SO4 and concentrated in vacuo to afford 4-(cyclopropylmethoxy)benzyl methanesulfonate (760 mg, 66% yield).
Step 4: A mixture of 6-methyl-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (300 mg, 1.29 mmol). 4-(cyclopropylmethoxy)benzyl methanesulfonate (429 mg. 1.68 mmol) and Cs2CO3 (841 mg, 2.58 mmol) in DMF (6 mL, anhydrous) was stirred at 60°C for 12 hours The mixture was filtered and the filtrate was concentrated under vacuum. The residue was purified by silica gel chromatography (column height: 250 mm, diameter: 100 mm, 100200 mesh silica gel, Petroleum ether/Ethyl acetate=10/1, 0/1) to give 7-(4(cyclopropylmethoxy)benzyl)-6-methyl-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin8(7H)-one (360 mg, 68% yield).
1H NMR (CDCI3, 400 MHz): <5 7.92 (s, 1H), 7.14 (d, J =8.8 Hz, 2H), 6.85 (d, J = 9.2 Hz, 2H),
6.73 (s, 1H), 5.16 (s, 2H), 4.12 (d, J = 10.8 Hz, 2H), 3.77 (d, J = 6.8 Hz, 2H), 3.61 - 3.55 (m, 2H), 3.10-3.04 (m, 1H), 2.20 - 2.09 (m, 5H), 1.88 (d, J = 13.2 Hz, 2H), 1.27 - 1.24 (m, 1H), 0.66 - 0.61 (m, 2H), 0.35 - 0.33 (m, 2H).
LC-MS: tR = 2.238 min (method 3), mlz = 394.1 [M + H]+.
Example 43:
7-benzyl-6-ethyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one:
A mixture of 6-ethyl-3-(tetrahydro-2/7-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (100 mg, 404 pmol), bromomethylbenzene (83 mg, 485.26 pmol) and Cs2CO3 (264 mg, 809 pmol) in DMF (3.0 mL) was stirred at 60°C for 16 hours. The reaction mixture was filtered and the filtrate was concentrated. The residue was purified by HPLC to give 7-benzyl-6-ethyl-3(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one (56.0 mg, 41.0% yield).
1H NMR (CDCI3 400 MHz): 5 7.91 (s, 1H), 7.32 - 7.26 (m, 3H), 7.22 - 7.15 (m, 2H), 6.69 (s, 1H), 5.25 (s, 2H), 4.12 (d, J= 10.8 Hz, 2H), 3 62-3.56 (m, 2H), 3.14-3.07 (m, 1H), 2.53 2.48 (m, 2H), 2.17 - 2.09 (m, 2H), 1.89 (d. J = 13.2 Hz, 2H), 1.22 (t, J = 7.2 Hz, 3H).
LC-MS: tR = 2.042 min (method 3), mlz - 338.2 [M + Hf.
Example 44:
6-ethyl-7-(4-methoxybenzyl)-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)one:
A mixture of 6-ethyl-3-(tetrahydiO-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (100 mg, 404 pmol), 1-(bromomethyi)-4-methoxy-benzene (98 mg, 485 pmol) and Cs2CO3 (264 mg, 809 prnol) in DMF (5.0 mL) was stirred at 60°C for 16 hours. The reaction mixture was filtered and the filtrate was concentrated. The residue was purified by HPLC to give 6-ethyl7-(4-methoxybenzyl)-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (65 mg, 42.3% yield).
1H NMR (CDCI3 400 MHz): 5 7.91 (s, 1H), 7.12 (d, J~ 8.0 Hz, 2H), 6.83 (d, J= 7.6 Hz, 2H), 6.68 (s, 1H), 5.18 (s, 2H), 4.12 (d, J = 11.6 Hz, 2H), 3.77 (s, 3H), 3.61 - 3.55 (m, 2H). 3.12 3.07 (m, 1H), 2.56-2.51 (m, 2H), 2.16-2.08 (m, 2H), 1.88 (d, J= 13.2 Hz, 2H), 1.22 (t, J =
7.2 Hz, 3H).
LC-MS: tR = 2.050 min (method 3), mlz = 368.2 [M + H]+.
Example 45:
3-((6-methyI-8-oxo-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-7(8H)yi)methyl)benzonitrile:
A mixture of 6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (100 mg, 428.69 pmol), 3-(bromomethyl)benzonitrile (126 mg, 643.03 pmol) and Cs2CO3 (279 mg, 858 pmol) in DMF (3 mL) was stirred at 70°C for 6 hours. The mixture was filtered and the filtrate was concentrated under vacuum. The residue was purified by preparative LC-MS to afford 3-((6-methyl-8-oxo-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-7(8H)yl)methyl)benzonitrile (35 mg, 23% yield).
1H NMR (CDCI3 400 MHz): o 7.95 (s, 1 H), 7.59 (d, J = 6.8 Hz, 1 H), 7.51 - 7.45 (m, 3H), 6.80 (s, 1H), 5.25 (s, 2H), 4.14 (d, J = 10.8 Hz, 2H), 3.63-3.57 (m, 2H), 3.14-3.08 (m, 1H), 2.19 -2.10 (m, 5H), 1.91 (d, J = 13.2 Hz, 2H).
LC-MS: fR = 2.164 min (method 3), m/z = 349.1 [M + H]+.
Example 46:
4-((6-methyl-8-oxo-3-(tetrahydro-2H-pyran-4-yl)imîdazo[1,5-a]pyrazin-7(8H)y1)methyl)benzonitrile:
A mixture of 6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (100 mg, 428.69 pmol), 4-(bromomethyl)benzonitrile (126 mg, 643.04 pmol) and Cs2CO3 (279 mg, 858 pmol) in DMF (3 mL) was stirred at 60°C for 2 hours. The mixture was filtered and the filtrate was concentrated under vacuum. The residue was purified by silica gel chromatography (petroleum ether/ethyl acetate=10/1, 1/5) to afford 4-((6-methyl-8-oxo-318771 (tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-7(8H)-yl)methyl)benzonitrile (65 mg, 43% yield).
1H NMR (CDCI3 400 MHz): δ 7.94 (s, 1 H), 7.64 (d, J = 8.0 Hz, 2H), 7.32 (d, J = 8.4 Hz, 2H), 6.79 (s, 1H), 5.28 (s, 2H), 4.14 (d, J = 11.2 Hz, 2H), 3.62-3.56 (m, 2H). 3.13-3.07 (m, 1H), 2.19 - 2.09 (m, 5H), 1.89 (d, J= 13.2 Hz, 2H).
LC-MS: fR = 2.160 mm (method 3), m/z = 349.2 [M + H]'.
Example 47:
A/-(4-((6-methyl-8-oxo-3-(tetrahydro-2H-pyran-4-yl)imidazo[1l5-a]pyrazin-7(8H)yl)methyl)phenyl)acetamide:
Step 1: A mixture of 6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (200 mg, 858 pmol), 1-(bromomethyl)-4-nitrobenzene (278 mg, 1.29 mmol) and Cs2CO3 (559 mg, 1.71 mmol) in DMF (4 mL) was stirred at 60°C for 2 hours. The mixture was filtered and the filtrate was concentrated under vacuum. The residue was purified by silica gel chromatography (petroleum ether/ethyl acetate=10/1, 1/5) to afford 6-methyl-7-(4nitrobenzyl)-3-(tetrahydro-2/7-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one (270 mg, 85% yield). LC-MS: tR = 0.612 min (method 2), m/z = 368.8 [M + H]+.
Step 2: A mixture of 6-methyl-7-(4-nitrobenzyl)-3-(tetrahydro-2/7-pyran-4-yl)imidazo[1,5a]pyrazin-8(7H)-one (200 mg, 542.90 pmol), Fe (152 mg, 2.71 mmol), NH4CI (88 mg, 1.63 mmol) and MeOH (10 mL) in H2O (10 mL) was stirred at 70°C for 4 hours. The mixture was filtered and the filtrate was concentrated under vacuum. The residue was purified by silica gel chromatography (dichloromethane /methanol=1/0, 15/1) to afford 7-(4-aminobenzyl)-6methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (170 mg, 93% yield). LC-MS: fR = 0.287 min (method 2), m/z = 338.9 [M + H]+.
Step 3: A mixture of 7-(4-aminobenzyl)-6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5a]pyrazin-8(7/7)-one (120 mg, 354.61 pmol), acetyl acetate (60 mg, 588.65 pmol) and triethylamine (144 mg, 1.42 mmol) in dioxane (10 mL) was stirred at 90°C for 6 hours. The solution was quenched with water (2 mL) and stirred at 60°C for 2 hours. Then it was concentrated under vacuum. The residue was purified by silica gel chromatography (dichloromethane / methanol=1/0, 15/1) to afford A/-(4-((6-methyl-8-oxo-3-(tetrahydro-2Hpyran-4-yl)imidazo[1,5-a]pyrazin-7(8H)-yl)methyl)phenyl)acetamide (120 mg, 86.52% yield).
Ή NMR (CDCI3 400 MHz): 5 7.92 (s. 1H). 7.44 (d. J = 8 4 Hz, 2H), 7.17 (d, J= 8.4 Hz, 2H),
6.74 (s, 1 H), 5.19 (s, 2H), 4.13 (d, J = 10.4 Hz, 2H), 3.59 (t, J= 10.0 Hz, 2H), 3.12-3.06 (m, 1H), 2.19-2.09 (m, 8H), 1.88 (d, J= 13.2 Hz, 2H).
LC-MS: = 1.593 min (method 3), mlz = 381.1 [M + H]*.
Example 48:
O
7-(4-chloro-3-methoxybenzyl)-6-methyl-3-(tetrahydro-2H-pyran-4-y!)imidazo[1,5a]pyrazin-8(7H)-one:
To a suspension of 6-methyl-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one (100 mg, 429 μιτιοΙ) in dry DMF (2 mL) was added Cs2CO3 (279 mg, 858 pmol) and 4(bromomethyl)-1-chloro-2-methoxybenzene (151 mg, 643 pmol). The mixture was purged with N2 for 2 min and heated at 60°C for 16 hours. The mixture was concentrated. DCM (30 ml) was added to the residue. It was filtered and the filter cake was washed with DCM (20 mL). The filtrate was concentrated and purified by flash chromatography on silica gel (10%-100% ethyl acetate in petroleum ether) to give 7-(4-chloro-3-methoxybenzyl)-6methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (99.01 mg, 60% yield).
1H NMR (CDCI3400 MHz); 5 7.93 (s, 1H), 7.30 (d, J= 8.4 Hz, 1H), 6.85 (d, J- 1.6 Hz, 1H),
6.75 (s. 1H), 6.72 - 6.69 (m, 1H), 5.17 (s, 2H), 4.14 - 4.11 (m, 2H), 3.86 (s, 3H), 3.61 - 3.55 (m, 2H), 3.10 - 3.06 (m, 1H), 2.20 (s, 3H), 2.18-2.11 (m, 2H), 1.89- 1.86 (m, 2H).
LC-MS: tR = 2.466 min (method 3), mlz = 388.1 [M + H]+.
Example 49:
7-(2-ethylbenzyi)-6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)one :
Step 1; A solution of (2-ethylphenyl)methanol (500 mg, 3.67 mmol) and triethylamine (742 mg, 7.34 mmol) in DCM (5 mL) was added MsCI (1.0 g, 8.73 mmol) at 0°C and stirred at 0°C for 0.5 hour. Then it was stirred at 20°C for 1 hour. The mixture was quenched with water (0.5 mL), and diluted with DCM (10 mL). The mixture was added NaHCO3 (aq.) until pH=8. The organic layer was washed with water (3 x 5 mL), dried with anhydrous Na2SO4, filtered and concentrated under vacuum to give 2-ethylbenzyl methanesulfonate (600 mg), which was used into the next step without further purification.
Step 2: A mixture of 6-methyl-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one (150 mg, 643 pmol), 2-ethylbenzyl methanesulfonate (276 mg) and Cs2CO3 (419 mg, 1.29 mmol) in DMF (5 mL) was stirred at 60°C for 12 hours. The mixture was filtered and the filtrate was concentrated under vacuum. The residue was purified by préparative LC-MS to afford 7-(2-ethylbenzyl)-6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)one (90 mg, 40% yield).
1H NMR (CDCI3 400 MHz): 5 7.93 (s, 1H), 7.25-7.21 (m, 2H), 7.14-7.10 (m, 1H), 6.81 6.77 (m, 2H), 5.25 (s, 2H), 4.14 (d, J = 11.2 Hz, 2H), 3.60 (t, J = 12.0 Hz, 2H), 3.15 - 3.09 (m, 1H), 2.78-2.72 (m, 2H), 2.21 - 2.13 (m. 5H), 1.91 (d, J = 13.6 Hz, 2H), 1.31 (t, J= 7.6 Hz, 3H).
LC-MS: fR = 2.533 min (method 3), m/z = 352.2 [M + H]+.
Example 50:
7-(6εηζο[ά][1,3^ΐοχοΙ-5-γΐΓΠβίΗγΙ)-6-ΠΊβίΙιγΙ-3-{ίΘίΓ3ΗγάΓθ-2Η-ργΓ3η-4-γΙ}ΪΓηΐά3Ζθ[1,5a] py razi η -8(7H)-o n e :
To a suspension of 6-methyi-3-(tetrahydro-2H-pyran-4-yl)imtdazo[1,5-a]pyrazin-8(7/-/)-one (100 mg, 429 pmol) in dry DMF (2 mL) was added Cs2CO3 (279 mg, 858 pmol) and 5(bromomethy!)benzo[d][1,3]dioxole (138 mg, 643 pmol). The mixture was bubbled with N2 for 2 min and heated at 60°C for 16 hours. The mixture was concentrated. DCM (30 mL) was added to the residue. It was filtered and the filter cake was washed with DCM (20 mL). The filtrate was concentrated and purified by flash chromatography on silica gel (10%~100% ethyl acetate in Petroleum ether) to give 7-(benzo[d]i1,3]dioxol-5-ylmethyl)-6-methyl-3(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (81.74 mg, 52% yield).
1H NMR (CDCl3 400 MHz): 57.92 (s, 1H), 6.76 - 6.69 (m, 4H), 5.95- 5.93 (m, 2H), 5.13 (s, 2H), 4.14 - 4.11 (m, 2H), 3.61 - 3.55 (m, 2H), 3.10 - 3.05 (m, 1H), 2.21 (s, 3H), 2.20 - 2.10 (m, 2H), 1.90- 1.86 (m, 2H).
LC-MS: tR = 2.245 min (method 3), m/z = 368.2 [M + H]+.
Example 51:
7-(3-chloro-4-methoxybenzyl)-6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5a]py razin-8(7 H)-one:
A mixture of 6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one (100 mg, 427 pmol), 4-(bromomethyl)-2-chloro-1-methoxybenzene (151 mg, 643 pmol) and Cs2CO3 (279 mg, 858 pmol) in DMF (3 mL) was stirred at 60°C for 2 hours. The mixture was filtered and the filtrate was concentrated under vacuum. The residue was purified by silica gel chromatography (detroleum ether/ethyl acetate=10/1, 0/1) to afford 7-(3-chloro-4methoxybenzyl)-6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (110 mg, 65% yieid).
1H NMR (CDCI3400 MHz): 57.93 (s, 1H), 7.24 (d, J= 0.8 Hz, 1H), 7.12 - 7.10 (m, 1H), 6.88 (d, J= 8.4 Hz, 1 H), 6.75 (s, 1H), 5.15 (s, 2H), 4.13 (d, J- 10.4 Hz, 2H), 3.88 (s, 3H), 3.62 3.56 (m. 2H). 3 12 - 3 06 (m. 1H). 2 20 - 2 09 (m. 5H), 1.89 (d, J= 13.2 Hz. 2H).
LC-MS: tR = 2.414 min (method 3), m/z = 388.1 [M + H]+.
Example 52:
o
7-(4-aminobenzyÎ)-6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)' one :
A solution of N-(4-((6-methyl-8-oxo-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-7(8H)yl)methyl)phenyl)acetamide (100 mg, 263 pmol), NaOH (63 mg, 1.58 mmol) and MeOH (1 mL) in H2O (1 mL) was stirred at 90°C for 12 hours. The solution was added KHSO< (aq.) until pH=7 and concentrated under vacuum. The residue was purified by préparative TLC (DCM: MeOH = 10:1). to afford 7-(4-aminobenzyl)-6-methyl-3-(tetrahydro-2/-/-pyran-4yl)imidazo[1,5-a]pyrazin-8(7H)-one (50 mg, 56% yieid).
1H NMR (CDCI3 400 MHz): 5 7.91 (s, 1H), 7.04 (d, J = 8.4 Hz, 2H), 6.71 (s, 1H), 6.63 (d, J = 8.4 Hz, 2H), 5.12 (s, 2H), 4.13 (d, J= 12.0 Hz, 2H), 3.67 (brs, 2H), 3.61 - 3.55 (m, 4H), 3.10 -3.05 (m, 1H), 2.21 (s, 3H), 2.17-2.08 (m, 2H), 1.88 (d, J =13.2 Hz, 2H).
LC-MS: tR = 1.273 min (method 3), m/z = 339.1 [M + Hf.
Example 53:
ο
7-(4-hydroxybenzyl)-6-methyl-3-(tetrahydro-2H-pyran^-yl)imidazo[1,5-a]pyrazin-8(7H)one:
A solution of 7-(4-methoxybenzyl)-6-methyl-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5a]pyrazin-8(7H)-one (2.0 g, 5.66 mmol) in DCM (32 mL) was added BBr3 (4.3 g, 16.98 mmol) at 0°C and stirred at 20°C for 3 hours. The solution was quenched with H2O (5 mL) at 0°C. The mixture was stirred at 0°C for 1 hour and then to it was added NaHCO3 (saturated aqueous) until pH=6. The mixture was concentrated under vacuum. The residue was diluted with DCM (20 mL) and MeOH (2 mL).Then it was filtered and the filtrate was concentrated under vacuum. The residue was added into KOH (60 mL, 2 M, aq.) at 20°C and stirred at 50°C for 1 hour. The solution was added KHSO4 (saturated aqueous) until pH=6, the mixture was concentrated under vacuum. The residue was purified by silica gel chromatography (dichloromethane/ methanol=1/0, 15/1) to afford 7-(4-hydroxybenzyl)-6-methyl-3-(tetrahydro2r/-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one (460 mg, 24% yield).
1H NMR (DMSO Varian_H_400 MHz): δ 9.39 (s, 1 H), 7.70 (s, 1 H), 7.46 (s, 1 H), 6.99 (d, J = 8.4 Hz, 2H), 6.70 (d, J = 8.4 Hz, 2H), 5.06 (s, 2H), 3.96 - 3.93 (m, 2H), 3.52 - 3.45 (m, 2H), 3.29- 3.16 (m, 1H), 2.15 (s, 3H), 1.83- 1.77 (m, 4H).
LC-MS: tR = 1.62 min (method 8), m/z = 340.1 [M + Hf.
Example 54:
6-ethyI-7-(3-fluorobenzyl)-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one:
Step 1: A mixture of methyl 1/7-imidazole-5-carboxylate (1.6 g, 13 mmol), l-bromobutan-2one (2.0 g, 13 mmol) and K2CO3 (3.5 g, 25 mmol) in acetone (20 mL) was stirred at 40*C for hours. The mixture was concentrated under vacuum. The residue was purified by silica gel chromatography (petroleum ether/ethyl acetate=10/1, 0/1) to give methyl 1-(2-oxobutyl)1/-/-imidazole-5-carboxylate (750 mg, 30% yield).
Step 2: A mixture of methyl 1-(2-oxobutyl)-1H-imidazole-5-carboxylate (700 mg, 3.59 mmol), NBS (831 mg, 4.67 mmol), and AIBN (118 mg, 718 pmol) in CHCI3 (20 mL) was stirred at 50eC for 12 hours The mixture was concentrated under vacuum. The residue was purified by silica gel chromatography (petroleum ether/ethyl acetate=10/1, 1/2) to give methyl 2bromo-1-(2-oxobutyl)-1/7-imidazole-5-carboxylate (650 mg, 66% yield). LC-MS: tR = 0.585 min (method 2), mlz = 274.7 [M + H]*
Step 3: A mixture of methyl 2-bromo-1-(2-oxobutyl)-1/-/-imidazole-5-carboxylate (650 mg, 2.36 mmol) and NH4OAc (727.64 mg, 9.44 mmol) in 1,4-dioxane (15 mL) was stirred at 90°C for 3 days. The mixture was concentrated under vacuum. The residue was purified by silica gel chromatography (petroleum ether/ethyl acetate=10/1, 1/1) to give 3-bromo-6ethylimidazo[1,5-a]pyrazin-8(7H)-one (500 mg, 88% yield). LC-MS: tR = 0.542 min (method 2), mlz = 241.8 [M + H]*
Step 4: A mixture of 3-bromo-6-ethylimidazo[1,5-a]pyrazin-8(7H)-one (500 mg, 2.07 mmol), 2-(3,6-dihydro-2H-pyran-4-yl)-4I4,5,5-tetramethyl-1,3,2-dioxaborolane (522 mg, 2.48 mmol), K2CO3 (572 mg, 4.14 mmol), Pd(dppf)CI2 (303 mg, 414 pmol) and H2O (5 mL) in 1,4dioxane (20 mL) was stirred at 100°C for 12 hours. The mixture was filtered and the filtrate was concentrated under vacuum. The residue was purified by silica gel chromatography (Dichloromethane/Methanol=1/0, 15/1) to give 3-(3,6-dihydro-2H-pyran-4-yl)-6ethylimidazo[1,5-a]pyrazin-8(7H)-one (400 mg, 78.78% yield). LC-MS: tR - 0.430 min (method 2), mlz = 245.8 [M + H]*
Step 5: A mixture of 3-(3,6-dihydro-2/7-pyran-4-yl)-6-ethylimidazo[1,5-a]pyrazin-8(7/7)-one (400 mg, 1.63 mmol) and Pd/C (dry, 10% Pd, 20 mg) in THF (15 mL) was stirred at 15°C for 4 hours under H2 (15 psi). The mixture was filtered and the filtrate was concentrated under vacuum to afford 6-ethyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (300 mg, 74% yield). LC-MS: fR = 1.324 min (method 9), mlz = 248.0 [M + H]*.
Step 6: A mixture of 6-ethyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (300 mg, 121 mmol), 1-(bromomethyl)-3-fluorobenzene (297 mg, 1.57 mmol) and K2CO3 (334 mg, 2.42 mmol) in DMF (20 mL) was stirred at 60°C for 12 hours. The mixture was filtered and the filtrate was concentrated under vacuum. The residue was purified by silica gel chromatography (Petroleum ether/Ethyl acetate=3/1, 0/1) to afford 6-ethyl-7-(318771 fluorobenzyl)-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (150 mg, 34% yield).
1H NMR (CDCI3 400 MHz): 5 7.94 (s, 1H), 7.32 -7.27 (m, 1H). 6.98-6.94 (m, 2H), 6.86 (d, J = 9.6 Hz, 1H), 6.72 (s, 1H), 5.25 (s, 2H), 4.14 (d, J= 11.2 Hz, 2H), 3.64-3.58 (m, 2H), 3.15 - 3.09 (m, 1H), 2.53-2.48 (m, 2H), 2.18-2.13 (m, 2H), 1.91 (d, J~ 13.2 Hz, 2H), 1.25 (t, J = 7.2 Hz. 2H)
LC-MS: tR = 2.475 min (method 3), m/z = 356.1 [M + Hf.
Example 55:
O
7-(4-methoxybenzyl)-6-methyl-3-(2-methyltetrahydrofuran-3-yl)imidazo[1,5-a]pyrazin8(7/ï)-one, stereoisomers 1,2,3 and 4:
Step 1: To a cooled (0°C) solution of 2-methyltetrahydrofuran-3-carboxylic acid (110 mg, 845 pmol) in dry DCM (2 mL) was added oxalyl dichloride (107 mg, 845 pmol) dropwise. Then one drop of DMF was added and the mixture was stirred at 26°C for 1 hour. The solution of 2-methy!tetrahydrofuran-3-carbonyl chloride (126 mg) in DCM (2 mL) was directly used for the next step.
Step 2: To a cooled (0°C) solution of 2-methyltetrahydrofuran-3-carbonyl chloride (160 mg, 844 pmol, HCl) in dry DCM (5 mL) was added triethylamine (256 mg, 2.53 mmol) and (3methoxy-5-methylpyrazin-2-yl)methanamine (125 mg, 843.70 pmol) in DCM (2 mL) dropwise. The mixture was stirred at 26°C for 1 hour. LCMS showed the reaction was completed. Water (5 mL) was added to the mixture. The mixture was extracted with DCM (30 mL * 2). The combined organic layer was washed with H2O (20 mL), brine (20 mL), dried over Na2SO4, filtered and concentrated. The crude product was purified by flash chromatography on silica gel (10-50% ethyl acetate in petroleum ether) to give N-((3methoxy-5-methylpyrazin-2-yl)methyl)-2-methyltetrahydrofuran-3-carboxamide (100 mg, 45% yield) as a light yellow oil.
Step 3: To a solution of A/-((3-methoxy-5-methylpyrazin-2-yl)methyl)-2methyltetrahydrofuran-3-carboxamide (150 mg, 565 pmol) in dry dioxane (5 mL) was added POCI3 (173 mg, 1.13 mmol). The mixture was heated at 80°C for 2 hours. The mixture was cooled to 26°C and the brown solution of 8-methoxy-6-methyl-3-(2-methyltetrahydrofuran-3yl)imidazo[1,5-a]pyrazine (140 mg) in dioxane (5 mL) was directly used for the next step.
Step 4: To a solution of 8-methoxy-6-methyl-3-(2-methyltetrahydrofuran-3-yl)imidazo[1.5a]pyrazine (140 mg, 566 pmol) in dioxane (5 mL) was added 2 N HCl (2 M, 2 mL). The mixture was heated at 80°C for 1 hour. The mixture was cooled to 25°C, adjusted to pH=7 by saturated aqueousNaHCO3 and extracted with DCM (20 mL χ 2). The combined organic phases were washed with H2O (20 mL), brine (20 mL), dried over Na2SO41 filter and concentrated to give 6-methyl-3-(2-methyltetrahydrofuran-3-yl)imidazo[1,5-a]pyrazin-8(7/7)one (131 mg).
Step 5: To a solution of 6-methyl-3-(2-methyltetrahydrofuran-3-yl)imidazo[1,5-a]pyrazin8(7H)-one (131 mg, 562 pmol) in dry DMF (5 mL) was added 1-(bromomethyl)~4methcxybenzene (169 mg, 842 pmol) and Cs2CO3 (366 mg, 1.12 mmol). The mixture was heated at 60°C for 16 hours. The mixture was concentrated and water (10 mL) was added. The mixture was extracted with DCM (30 mL χ 2). The combined organic layer was washed with H2O (30 mL χ 2), brine (30 mL), dried over Na2SO4, filtered and concentrated. The residue was purified by flash chromatography on silica gel (10%~100% ethyl acetate in petroleum ether) to give 7-(4-methoxybenzyl)-6-methyl-3-(2-methyltetrahydrofuran-3yl)imidazo[1,5-a]pyrazin-8(7/-0-one (90 mg, 45% yield).
7-(4-methoxybenzyl)-6-methyl-3-(2-methyltetrahydrofuran-3-yl)imidazo[1,5-a]pyrazin-8(7H)one (100 mg, 283 pmol) was purified by SFC.
Stereoisomer 1: (9.4 mg, 9% yield).
1H NMR (CDCI3400 MHz): 57.92 (s, 1H), 7.15 (d, J= 8.8 Hz, 2H), 6.84 (d, J= 8.4 Hz, 2H), 6.74 (s, 1H), 5.16 (s, 2H), 4.30-4.26 (m, 1H), 4.12-4.04 (m, 2H), 3.78 (s, 3H), 3.09-3.03 (m, 1 H), 2.46-2.34 (m, 2H), 2.20 (s, 3H), 1.32 (d, J= 6.0 Hz, 3H).
LC-MS: tR = 2.074 min (method 13), m/z = 354.1 [M + H]+. SFC: tR = 5.177 min, ee% > 99%. [a]D 20 -26 (c = 0.10, DCM).
Stereoisomer 2: (7.3 mg, 7% yield) .
100
H NMR (CDCI3 400 MHz): δ 7.92 (s, 1 H), 7.15 (d, J= 8.8 Hz, 2H), 6.84 (d, 8.4 Hz, 2H),
6.73 (s, 1H), 5.16 (s, 2H), 4.30-1.26 (m, 1H), 4.10-4.02 (m, 2H), 3.78 (s, 3H), 3.09-3.03 (m, 1H), 2.44-2.35 (m, 2H). 2.20 (s, 3H), 1.32 (d, J= 6.0 Hz, 3H).
LC-MS: tR = 2.072 min (method 13), mlz = 354.1 [M + Hf. SFC: fR = 5.458 min, ee% = 99.7%. [a]D 20 +24 (c = 0.10, DCM).
Stereoisomer 3: (39.7 mg, 40% yield).
Ή NMR (CDCI3 400 MHz): 5 7.92 (s. 1H). 7.15 (d. J= 8.4 Hz. 2H), 6.84 (d, J= 8.4 Hz, 2H), 6.78 (s. 1H), 5.22-5.10 (m, 2H), 4.31-4.26 (m, 2H). 3.88-3.82 (m, 1H), 3.77 (s, 3H), 3.70-3.60 (m, 1H), 2.71-2.67 (m, 1H), 2.43-2.40 (m, 1H), 2.19 (s, 3H), 0.87 (d, J= 4.4 Hz, 3H).
LC-MS: tR = 1.983 min (method 13), mlz = 354.1 [M + H]*. SFC: tR = 5.932 min, ee% = 98.8%. [a]D 20 +48 (c = 0.10, DCM).
Stereoisomer 4: (26.4 mg, 26% yield) .
’H NMR (CDCI3400 MHz): 5 7.92 (s, 1H), 7.15 (d, J= 8.8 Hz, 2H), 6.84 (d, 8.4 Hz, 2H),
6.78 (s, 1H), 5.22-5.09 (m, 2H). 4.32-4.26 (m, 2H), 3.87-3.85 (m, 1H), 3.77 (s, 3H), 3.68-3.64 (m. 1H), 2.70-2.65 (m, 1H), 2.42-2.37 (m, 1H), 2.19 (s, 3H), 0.87 (d, J= 6.4 Hz, 3H).
LC-MS: tR = 1.983 min (method 13), mlz = 354.1 [M + H]+. SFC: tR = 6.570 min, ee% = 99.6%. [a]D 20 -64 (c = 0.10, DCM).
Example 56:
O
7-(4-methoxybenzyl)-6-methyl-3-propylimidazo[1,5-a]pyrazin-8(7H)-one:
To a solution of 3-bromo-7-(4-methoxybenzyl)-6-methylimidazo[1,5-a]pyrazin-8(7/-/)-one (500 mg, 1.44 mmol, 1 eq) in THF (10 mL) was added Ni(dppp)CI2 (327.83 mg, 604.80 pmol, 0.42 eq) at 0°C over 10 min, then at -78°C for 10 min. propylmagnesium bromide (1 M, 3 mL, 2.1 eq) was added dropwise at 0°C. The resulting mixture was stirred at 0°C for 1.5 hour. The reaction was quenched by saturated NH4CI aqueous solution (5 mL). The residue
101 was purified by silica column chromatography (Gradient: 0-50, EtOAc in PE with 1% triethylamine) to give 220 mg of crude product. The crude product was purified by préparative TLC ( PE:EtOAc=1:1 with 1% triethylamine). The residue was washed with hexane (3 mL) and filtered and the filter cake was dried under vacuum to give 7-(4methoxybenzyl)-6-methyl-3-propy1imidazo[1.5-a]pyrazin-8(7/-/)-one (82 mg, 18% yield).
’HNMR (CDCI3. 400 MHz): 5 7.90 (s. 1H), 7.16 (d. J = 8 8. 2H), 6 85 (d. J = 8.8, 2H). 6.68 (s, 1H), 5.17 (s, 2H), 3.78 (s, 3H), 2.82 (t, J = 7.2, 2H), 2.19 (s, 3H), 1.90-1.81 (m, 2H), 1.03 (t, J = 7.2, 3H)
LC-MS: tR = 1.927 min (method 13), m/z = 312.1 [M + H]'.
Example 57:
O
7-((6-methoxypyridin-3-yl)methyl)-6-methyl-3-(tetrahydrO’-2H-pyran-4-yl)imidazo[1,5a]pyrazin-8(7H)-one:
Into a vial was added 6-methyl-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one (200mg, 0.86 mmol), 5-(chloromethyl)-2-methoxypyridine (162 mg, 1.03 mmol), césium carbonate (559 mg, 1.72 mmol) and sodium iodide (154 mg, 1.03 mmol) in DMF (9.44 g, 10 ml, 129 mmol). The reaction was stirred overnight at 70°C. To the reaction was added ethylacetate, and it was filtered and concentrated. The reaction was purified by chromatography on silicagel to obtain 7-((6-methoxypyridin-3-yl)methyl)-6-methyl-3(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (127 mg, 0.358 mmol) in 42% yield.
1H NMR (600 MHz, CDCI3) δ 8.06 (dd, J = 2.5, 0.8 Hz, 1 H), 7.91 (d, J = 0.6 Hz, 1 H), 7.55 (dd, J= 8.6, 2.5 Hz, 1H), 6.74 (t, J= 1.1 Hz, 1H), 6.71 (dd, J= 8.6, 0.7 Hz, 1H), 5.15 (s. 2H), 4.12 (m, 2H), 3.91 (s, 3H), 3.58 (td, J = 11.7, 2.2 Hz, 2H), 3.07 (tt, J= 11.4, 3.9 Hz, 1H), 2.25 (d, J= 1.2 Hz, 3H), 2.12 (dtd, J= 13.7, 11.6, 4.3 Hz, 2H), 1.87 (ddd, J = 13.5, 4.2, 2.1 Hz, 2H).
102
LC-MS: fR = 0.38 min (method 6), m/z - 355.2 [M + Hf.
Example 58:
O
II
6,7-dimethyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one:
To a solution of 6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (100 mg, 428.69 pmol, 1 eq) in DMSO (2 mL) was added Cs2CO3 (139.68 mg, 428.69 pmol, 1 eq) and methyliodide(121.70 mg, 858 pmol, 53.38 pL, 2 eq) .The mixture was stirred at 50 CC for 12 hour .The reaction mixture was diluted with H2O (25mL) and extracted with DCM (50 mL * 2) The combined organic layers were washed with brine (15 mL), dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by preparative TLC (ethyl acetate). 6,7-dimethyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5a]pyrazin-8(7H)-one (73 mg, 68% yield, 98% purity) was obtained.
1H NMR (CDCI3 400 MHz): δ 7.87 (s, 1 H), 6.76 (s, 1 H), 4.13 (d, J = 11.2 Hz, 2H), 3.59 (t, J = 11.2 Hz, 2H), 3.46 (s, 3H), 3.11-3.05 (m, 1 H), 2.28 (s, 3H), 2.16-2.08 (m, 2H), 1.88 (d, J = 14.0 Hz, 2H).
LC-MS: (R = 1.300 min (method 13), m/z = 248.1 [M + H]+.
Example 59:
7-ethyl-6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one:
103
To a solution of 6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (100 mg, 429 pmol, 1 eq) in anhydrous DMF (2 mL) was added K2CO3 (119 mg, 858 pmol, 2 eq) and iodoethane (134 mg, 858 pmol, 69 pL, 2 eq).The mixture was stirred at 50°C for 12 hour. The reaction mixture was concentrated under reduced pressure. The residue was diluted with H2O (20 mL) and extracted with EA(40 mL * 2). The combined organic layers were washed with brine(15 mL), dried over Na2SO4, filtered and concentrated under reduced pressure to afford a residue 7-ethyl-6-methyl-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5a]pyrazin-8(7H)-one (40 mg, 34% yield, 96% purity) was obtained.
NMR (CDCI3 400 MHz): 5 7.85 (s. 1 H), 6.73 (s. 1H), 4,12 (d, J= 10.8 Hz, 2H), 4.03-3.99 (m, 2H), 3.58 (t, J= 10.8 Hz, 2H), 3.10-3.04 (m, 1H), 2.30 (s, 3H), 2.16-2.07 (m, 2H), 1.87 (d, J= 13.2 Hz, 2H), 1.29 (t, J = 6.8 Hz, 3H).
LC-MS: fR = 1.490 min (method 11), mlz = 262.1 [M + Hf.
Example 60:
O
N
N
O
6-methyl-7-propyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one:
To a solution of 6-methyl-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one (100 mg, 429 pmol, 1 eq) in anhydrous DMF (2 mL) was added K2CO3 (119 mg, 858 pmol, 2 eq) and 1-bromopropane (105 mg, 858 pmol, 78,11 pL, 2 eq).The mixture was stirred at 50 °C for 12 hours.The reaction mixture was concentrated under reduced pressure to remove DMF. The residue was diluted with H2O (20 mL) and extracted with EA(40 mL* 2). The combined organic layers were washed with brine (15 mL), dried over Na2SO4, filtered and concentrated under reduced pressure.The restdue was purified by préparative TLC (ethyl acetate). 6-methyl-7-propyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (45 mg, 37% yield, 98% purity) was obtained.
104
Ή NMR (CDCI3400 MHz): 5 7.85 (s, 1H), 6.72 (s, 1H), 4.12 (d, J = 10.4 Hz, 2H), 3.88 (t, J = 8.0 Hz ,2H), 3.62-3.56 (m, 2H), 3.10-3.07 (m, 1H), 2.28 (s, 3H), 2.14-2.09 (m, 2H), 1.87 (d, J = 13.2 Hz, 2H), 1.73-1.67 (m, 2H), 1.00 (t, J = 7.2 Hz, 3H).
LC-MS: fR = 1.666 min (method 11), m/z = 276.1 [M + H]+.
Example 61:
7-i3opropyl-6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one:
To a solution of 6-methyl-3-(tetrahydro-2H-pyran-4-yi)imidazo[1,5-a]pyrazin-8(7H)-one (350 mg, 1.50 mmol, 1 eq) in anhydrous DMF (4 mL) was added Cs2CO3 (978 mg, 3 mmol, 2 eq) and 2-iodopropane (510 mg, 3 mmol, 300 pL, 2 eq).The mixture was stirred at 50 °C for 12 hours.The reaction mixture was concentrated under reduced pressure to remove DMF. The residue was diluted with H2O (15mL) and extracted with EtOAc(40mL χ 2). The combined organic layers were washed with brine(10 mL), dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by préparative TLC (ethyl acetate). 7isopropyl-6-methyl-3-(tetrahydro-2/7-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (68 mg, 16% yield, 96% purity) was obtained.
1H NMR (CDCl3 400 MHz): 57.81 (s, 1H), 6.67 (s, 1 H), 4.40 (m, 1H), 4.12 (d, J- 11.6 Hz, 2H), 3.58 (t, J = 11.3 Hz ,2H), 3.09-3.03 (m, 1 H), 2.27 (s, 3H), 2.14-2.06 (m, 2H), 1.86 (d, J =
13.2 Hz, 2H), 1.62-1.61 (m, 6H).
LC-MS: = 1.576 min (method 13), mlz- 276.1 [M + H]*.
105
Example 62:
T-isopentyl-e-methyl-SHtetrahydro^H-pyran^-ynimidazoIl.S-alpyrazin-etTHJ-one:
To a solution of 6-methyl-3-(tetrahydro-2H-pyran^-yl)imidazo[1,5-a]pyrazin-8(7H)-one (100 mg, 428.69 pmol, 1 eq) in anhydrous DMF (2 mL) was added K2CO3 (118.50 mg, 858 pmol, 2 eq) and 1-bromo-3-methylbutane (129.50 mg, 858 pmol, 108 pL, 2 eq).The mixture was stirred at 50 °C for 12 hours. The reaction mixture was concentrated under reduced pressure to remove DMF. The residue was diluted with H2O (20 mL) and extracted with EtOAc(40 mL * 2). The combined organic layers were washed with brine(15 mL), dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by preparative TLC (ethyl acetate). 7-isopentyl-6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin8(7F/)-one (65 mg, 50% yield) was obtained.
1H NMR (CDCI3 400 MHz): 57.84 (s, 1H), 6.73 (s, 1H), 4.12 (d, J= 10.4 Hz, 2H), 3.93 (t, J = 8.0 Hz ,2H), 3.61-3.55 (m, 2H), 3.08-3.04 (m, 1H), 2.28 (s, 3H), 2.10-2.09 (m, 2H), 1.87 (d, J = 14.0 Hz, 2H), 1.74-1.69 (m. 1H), 1.56-1.52 (m, 2H), 1.00-0.98 (m, 6H).
LC-MS: fR = 1.968 min (method 13), mlz = 304.2 [M + Hf.
Example 63:
O
106
7-(cyclopentylmethyl)-6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin8(7H)-one:
To a mixture of 6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (150 mg, 0.64 mmol) and (bromomethyl)cyclopentane (157 mg, 0.96 mmol) in DMSO (2 mL) was added Cs2CO3 (419 mg, 1.29 mmol). The mixture was stirred at 60 °C for 12 hours. The mixture was diluted with water (10 mL) and extracted with DCM (5 mL * 3). The combine organic layer was washed with water (5 mL χ 2) and dried over Na2SO4. The organic layers was evaporated under vacuum. The residue was purified by preparative TLC (ethyl acetate) to give 7-(cycîopentylmethyl)-6-methyl-3-(tetrahydro-2/7-pyran-4-yl)imidazo[1,5-a]pyrazin8(7/7)-one (95 mg, 46% yield). ’HNMR (CDCI3, 400 MHz): δ 7.85 (s, 1H), 6.72 (s, 1H), 4.144.11 (m. 2H), 3.91 (d, J = 7.6 Hz, 2H), 3.61-3.56 (m, 2H), 3.12-3.05 (m, 1H), 2.29 (s, 3H), 2.27-2.25 (m, 1H), 2.14-2.10 (m, 2H), 1.90-1.86 (m, 2H), 1.71-1.54 (m, 6H), 1.34-1.32 (m, 2H).
LC-MS: tR = 1.98 min (method 13), m/z = 316.2 [M + H]+.
Example 64:
2-((6-methyl-8-oxo-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-7(8H)yl)methyl)benzonitrile:
A mixture of 6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (100 mg, 429 pmol), 2-(bromomethyl)benzonitriIe (126 mg, 643 pmol) and Cs2CO3 (279 mg, 857 pmol) in DMF (3.0 mL) was stirred at 70°C for 6 hours. The mixture was filtered and the filtrate was concentrated under vacuum. The residue was purified by silica gel chromatography (Petroleum ether/Ethyl acetate=10/1, 0/1) to afford 2-((6-methyl-8-oxo-3(tetrahydro-2H-pyran^-yl)imidazo[1,5-a]pyrazin-7(8H)-yl)methyl)benzonitrile (92 mg, 59% yield).
107 1H NMR (CDCI3 400 MHz): δ 7.96 (s, 1 H), 7.72 (d, J = 7.6 Hz, 1 H), 7.55 (t, J = 7.2 Hz, 1 H), 7 40 (t, J=7.2 Hz, 1H), 7.19 (d, J = 8.0 Hz, 1H), 6.80 (s, 1H), 5.45 (s, 2H), 4.14 (d, J = 12.0 Hz, 2H), 3.63 -3.57 (m, 2H), 3.14-3.08 (m, 1H), 2.20-2.09 (m. 5H), 1.90 (d, J= 13.2 Hz, 2H).
LC-MS: tR = 2.202 min (method 3), mlz= 349.1 [M + HJ*.
Example 65:
7-(cycloheptylmethyl)-6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin8(7H)-one:
Step 1: To a solution of cycloheptanecarboxylic acid (500 mg, 3.52 mmol) in THF (40 mL) was added LiAIH4 (401 mg, 10.6 mmol) in portions at 0 °C. The mixture was stirred at 65 °C for 3 hours. The reaction was quenched with H2O (0.4 mL) and 10% NaOH (0.4 mL, aq). To the mixture was added Na2SO4. The mixture was filtered. The filtrate was concentrated. The residue was purified by flash silica gel chromatography to give cycloheptylmethanol (383 mg, 85% yield).
'H NMR (CDCI3 400 MHz): δ 3.43 (d. J = 6.4 Hz, 2H), 1.80-1.62 (m, 5H), 1.56- 1.40 (m, 4H), 1.31 (br, s, 1H), 1.84 (s, 3H), 1.10- 1.22(m, 2H).
Step 2: To a solution of cycloheptylmethanol (313 mg, 2.44 mmol) and triethylamine (494 mg, 4.88 mmol) in DCM (5 mL) was added MsCI (490 mg, 4.28 mmol) at 0 °C and it was stirred at 20 °C for 40 min. The solution was washed with NaHCO3 (saturated aqueous 5mL x 4), water (5 mL χ 2), brine (3 mL) and then was dried over Na2SO4, filtered and concentrated to give cycloheptylmethyl methanesulfonate (381 mg) which was used in the next step directly without further purification.
Step 3: To a solution of 6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)one (150 mg, 643 pmol) and cycloheptylmethyl methanesulfonate (159 mg, 772 pmol) in DMF (3 mL) was added Cs2CO3 (419 mg, 1.29 mmol). The mixture was stirred at 60 °C for 6
108 hours. The mixture was diluted with DCM (20 mL) and washed with water (5 mL * 2), brine (10 mL), dried over Na2SO4, filtered and concentrated. The residue was purified by flash silica gel chromatography and then was purified by preparative LC-MS to give 7(cycloheptylmethyl)-6-methyl-3-(tetrahydro-2/7-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (25.15 mg, 11% yield).
’H NMR (CDCIs 400 MHz): 5 7.84 (s. 1H). 6 71 (s. 1H), 4 12 (d. J= 5.2 Hz. 2H), 3.77 (d. J =
3.6 Hz. 2H). 3.65 - 3.52 (m, 2H), 3.15 - 3.02 (m, 1H), 2.26 (s, 3H), 2.17 - 2.07 (m, 2H). 2.07 2.98 (m. 1 H), 1.87 (d. J = 6.6 Hz. 2H). 1.63 - 1.75 (m. 4H), 1.55 - 1.62 (m, 2H), 1.54 - 1.45 (m, 2H), 1.44- 1.33 (m, 2H). 1.30- 1.18 (m, 2H).
LC-MS: tR = 2.227 min (method 13), m/z = 344.2 [M + Hf.
Example 66:
6-methyl-7-((4-methylcyclohexyl)methyl)-3-(tetrahydro-2H-pyran-4-yI)imidazo[1,5a]pyrazin-8(7H)-one, cis and trans:
Step 1: To a solution of (4-methylcyclohexyl)methanol (400 mg, 3.12 mmol, 1 eq) in anhydrous DCM (20 mL) was added triethylamine (631 mg, 6.24 mmol, 865 pL, 2 eq) .The mixture was dropwise added methanesulfonyl chloride (465 mg, 4.06 mmol, 314 pL, 1.30 eq) at 0°C and it was stirred at 0 °C for 1 hour. The reaction mixture was washed with water (5mL χ 3), brine (3mL), dried and concentrated. (4-methylcyclohexyl)methyl methanesulfonate (700 mg) was obtained.
Step 2: To a solution of 6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)one (260 mg, 1.11 mmol, 1 eq) and (4-methylcyclohexyl)methyl methanesulfonate (572 mg, 2.78 mmol, 2.50 eq) in anhydrous DMF (6 mL) was added Cs2CO3 (723 mg, 2.22 mmol, 2 eq). The mixture was stirred at 60 °C for 12 hours. The reaction mixture was concentrated under reduced pressure to remove DMF. The residue was diluted with H2O (3 mL) and extracted with DCM (10 mL x 2). The combined organic layers were dried over Na2SO4
109 .filtered and concentrated The residue was purified by préparative TLC (SiOj, EA). 6nnetliyl-7-((4-methylcyclohexyl)methyl)-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin8(7H)-one (175 mg, 45% yield) was obtained.
trans-6-methyl-7-((-4-methylcyclohexyl)methyl)-3-(tetrahydro-2H-pyran-4yl)imidazo[1,5-a]pyrazin-8(7H)-one:
6-methyl-7-((4-methylcyclohexyl)methyl)-3-(tetrahydro-2H-pyran-4-yl)imidazo[1l5-a]pyrazin8(7H)-one (160 mg, 466 pmol, 1 eq) was purified by SFC to give 6-methyl-7-(((trans)-4methyicyclohexyl)methyl)-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (60 10 mg, 37% yield, 98% purity).
’H NMR (CDCI3 400 MHz): 5 7.84 (s, 1H), 6.71 (s, 1H), 4.12 (d, J = 10.8 Hz, 2H), 3.79-3.77 (m, 2H), 3.61-3.55 (m, 2H), 3.09-3.05 (m, 1H), 2.26 (s, 3H), 2.14-2.07 (m, 2H), 1.88 (d, J = 10.8 Hz, 2H), 1.69-1.67 (m, 5H), 1.34-1.32 (m, 2H), 1.11-1.09 (m, 2H), 0.91-0.86 (m, 4H).
LC-MS: tR = 2.256 min (method 13), mlz = 344.2 [M + H]+.
O
c/s-e-methyl-T-ft^-methylcyclohexyllmethyO-S-ttetrahydro-aH-pyran-A-ynimidazotl.Sa]pyrazin-8(7H)-one:
6-methyl-7-(((c/s)-4-methylcyclohexyl)methyl)-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5a]pyrazin-8(7H)-one (90 mg, 54% yield).
110 1H NMR (CDCI3 400 MHz): 5 7.85 (s, 1 H), 6.72 (s, 1H), 4.12 (d, J= 10.8 Hz, 2H), 3.89-3.87 (m, 2H), 3.61-3.55 (m, 2H), 3.09-3.05 (m, 1H), 2.28 (s, 3H), 2.14-2.11 (m, 2H), 1.87 (d, J = 14.4 Hz, 2H), 1.50-1.40 (m, 8H), 0.97-0.95 (m, 3H).
LC-MS: fR = 2.240 min (method 13), m/z = 344.2 [M + H]4.
Example 67:
O
7-{((cis)-4-methoxycyclohexyl)methyl)-6-methyl-3-(tetrahydro-2H-pyran-4yl)imidazo[1,5-a]pyrazin-8(7H)-one:
To a solution of 6-methyl-3-(tetrahydro-2,H-pyran-4-yl)Îmidazo[1,5-a]pyrazin-8(7/-/)-one (60 mg, 257 pnnol, 1 eq) in dry DMF (5 mL) was added ((cis)-4-methoxycyclohexyl)methyl methanesulfonate (74 mg, 334 pmol, 1.30 eq) and Cs2CO3 (168 mg, 514 pmol, 2 eq). The mixture was heated at 60°C for 16 hours. The mixture was concentrated. DCM (20 mL) and H2O (10 mL) was added. The mixture was extracted with DCM (20 mL). The organic layer was washed with H2O (20 mL), dried over Na2SO4, filtered and concentrated. The residue was purified by préparative TLC (DCM/MeOH=20/1) to give 7-(((c/s)-4methoxycyclohexyl)methyl)-6-methyl-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin8(7H)-one (15 mg, 16% yield).
1H NMR (CDCI3 400 MHz): 5 7.83 (s, 1H), 6.69 (s, 1H), 4.10 (d, J = 11.2 Hz, 2H), 3.75 (d, J =
7.2 Hz, 2H), 3.56 (t, J= 11.2 Hz, 2H), 3.42 (m, 1H), 3.29 (s, 3H), 3.11-3.03 (m, 1H), 2.24 (s, 3H), 2.15-2.06 (m, 2H), 1 94-1.84 (m, 5H),1.44-1.37 (m, 6H).
LC-MS: fR = 1.887 min (method 13), m/z = 360.2 [M + H]4.
111
Example 68:
7-(((frans)-4-methoxycyclohexyl)methyl)-6-methyl-3-(tetrahydro-2H-pyran-4yl)imidazo[1,5-a]pyrazin-8(7H)-one:
To a solution of 6-methyl-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/7)-one (60 mg, 257 pmol, 1 eq) in dry DMF (5 mL) was added ((trans)-4-methoxycyclohexyl)methyl methanesulfonate (74 mg, 334 pmol, 1.30 eq) and Cs2CO3 (168 mg, 514 pmol, 2 eq). The mixture was heated at 60°C for 16 hours. The mixture was concentrated. DCM (20 mL) and H2O (10 mL) were added. The mixture was extracted with DCM (20 mL). The organic layer was washed with H2O (20 mL), dried over Na2SO4, filtered and concentrated. The residue was purified by préparative TLC (DCM/MeOH=20/1) togive 7-(((trans)-4methoxycyc!ohexyl)methyl)-6-methyl-3-(tetrahydro-2/7-pyran-4-yI)imidazo[1,5-a]pyrazin8(7H)-one (35 mg, 38% yield).
1H NMR (CDCI3 400 MHz): <57.84 (s, 1H), 6.71 (s, 1H), 4.11 (d, J= 10.4 Hz, 2H), 3.79 (d, J =
5.6 Hz, 2H), 3.57 (t, J = 10.0 Hz, 2H), 3.33 (s, 3H), 3.10-3.05 (m, 2H), 2.26 (s, 3H), 2.15-2.07 (m, 4H), 1.88-1.84 (m. 2H),1.75-1.71 (m, 3H), 1.15-1.11 (m, 4H).
LC-MS: tR = 1.831 min (method 13), m/z ~ 360.2 [M + H]*.
Example 69:
O
112
7- (4-methoxybenzyl)-6-methyl-3-(3-methyltetrahydro-2H-pyran-4-yl)imidazo[1,5a]pyrazin-8(7H)-one:
Step 1: To a solution of (3-methoxy-5-methylpyrazin-2-yl)methanamine hydrochloride (150 mg, 0.79 mmol, 1 eq) and 3-methyltetrahydro-2H-pyran-4-carboxylic acid (125 mg, 870 pmol, 1.1 eq) in DCM (5 mL) was added HATU (451 mg, 1.19 mmol, 1.5 eq) and DIPEA (204 mg. 1 58 mmol, 276 pL, 2 eq) The mixture was stirred at 25 °C for 18 hours The mixture was concentrated. The crude product was purified by flash chromatography with Petroleum ethenethyl acetate = 3:1 -2:1. A/-((3-methoxy-5-methylpyrazin-2-yl)methyl)-3methyltetrahydro-2/-/-pyran-4-carboxamide (220 mg, 780 pmol, 99% yield) was obtained.
Step 2: To a solution of A/-((3-methoxy-5-methylpyrazin-2-yl)methyl)-3-methyltetrahydro-2/-/pyran-4-carboxamide (220 mg, 788 pmol, 1 eq) in dioxane (8 mL) was added POCI3 (242 mg, 1.58 mmol, 146 pL, 2 eq). The mixture was stirred at 80 °C for 2 hours. The mixture was concentrated. 6-methyl-3-(3-methyltetrahydro-2/7-pyran-4-yl)imidazo[1,5-a]pyrazin-8-ol (223 mg, hydrochloride sait) was used in the next step without further purification.
Step 3: To a solution of 6-methyl-3-(3-methyltetrahydro-2/7-pyran-4-yl)imidazo[1,5-a]pyrazin- '*
8- ol (170 mg, 0 6 mmol) in DMF (5 mL) was added Cs2CO3 (586 mg, 1.80 mmol, 3 eq) and ΐ i-(chloromethyl)-4-rnethoxybenzene (113 mg, 719 pmol, 98 pL, 1.20 eq). The mixture was stirred at 60°C for 18 hours. The reaction mixture was filtered, and the filtrate was concentrated. The crude mixture was purified by préparative LC-MS,and then by préparative TLC with ethyl acetate as eluent. 7-(4-methoxybenzyl)-6-methyl-3-(3methyltetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one (76 mg, 207 pmol, 35% yield) was obtained.
1H NMR, a mixture of diastereoisomers (CDCI3400 MHz): δ 7.96 - 7.94 (m, 1H), 7.18 (d, J = 8.0 Hz, 2H), 6.86 (d, J = 8.0 Hz, 2H), 6.76 (s, 0.73H), 6.71 (s, 0.28H), 5.22 - 5.12 (m, 2H). 4.17-4.01 (m, 2H), 3.79 (s, 3H), 3.55- 3.49 (m. 1H). 3.19-3.14 (m, 1 H), 2.66 - 2.64 (m, 1H), 2.36 -2.33 (m, 1H), 2.21 (s, 3H), 2.13-2.10 (m, 1H), 1.78-1.61 (m, 1H), 0.87 (d, J =
7.2 Hz, 1 H), 0.71 (d, J = 6.8 Hz, 2H).
LC-MS: îr = 2.370 min (method 11), m/z =368.1 [M + Hf.
Example 70:
113
Ο
racemîc 7-i4-methoxybenzyl)-6*methyl-3-((1F?)2Rl4S)-2-methyl-7oxabicyclo[2.2.1]heptan-2-yl)imidazo[1,5-a]pyrazin-8(7H)-one:
Step 1: To a solution of (3-methoxy-5-methylpyrazin-2-yl)methanamine hydrochloride (150 mg, 791 pmol, 1 eq) in dry DCM (5 mL) was added triethylamine (240 mg, 2.37 mmol, 329 pL, 3 eq), racemic (1/?,2S,4S)-2-methyl-7-oxabicyclo[2.2.1]heptane-2-carboxylic acid (124 mg. 791 pmol, 1 eq) and HATU (361 mg, 949 pmol, 1.20 eq). The mixture was stirred at 15°C for 16 hours. H2O (5 mL) was added and the mixture was extracted with DCM (20 mL χ 2). The combined organic layer was washed with H2O (20 mL), brine (20 mL), dried over Na2SO4, filtered and concentrated, The residue was purified by flash chromatography on silica gel (0%~50% ethyl acetate in petroleum ether) to give racemic (1R,2S,4S)-A/-((3methoxy-5-methylpyrazin-2-yl)methyl)-2-methyl-7-oxabicyclo[2.2.1]heptane-2-carboxamide r. (200 mg, 87% yield).
Step 2: To a solution of racemic (1R,2S,4S)-A/-((3-methoxy-5-methylpyrazin-2-yl)methyl)-2methyl-7-oxabicyclo[2.2.1]heptane-2-carboxamide (150 mg, 515 pmol, 1 eq) in dry dioxane (5 mL) was added POCI3 (158 mg, 1.03 mmol, 96 pL, 2 eq). The mixture was heated at 80°C for 2 hours. The mixture was cooled to 15°C and poured into water (5 mL). The mixture was adjusted to pH 8 by saturated aqueous NaHCO3 and extracted with DCM (20 mL χ 2). The combined organics were washed with H2O (20 mL), brine (20 mL), dried over Na2SO41 filtered and concentrated to give racemic 6-methyl-3-((1R,2R,4S)-2-methyl-7oxabtcyclo[2.2.1]heptan-2-yl)imidazo[1,5-a]pyrazin-8-ol (120 mg).
Step 3: To a solution of racemic 6-methyl-3-((1R,2F?,4S)-2-methyl-7-oxabicyclo[2.2.1]heptan2-yl)imidazo[1,5-a]pyrazin-8-ol (100 mg, 386 pmol, 1 eq) in dry DMF (5 mL) was added 1(chloromethyl)-4-methoxy-benzene (72 mg, 463 pmol, 63 pL, 1.20 eq) and Cs2CO3 (251 mg, 771 pmol, 2 eq). The mixture was heated at 60°C for 2 hours. The mixture was concentrated. DCM (20 mL) and H2O (10 mL) was added. The mixture was extracted with DCM (20 mL). The organic layer was washed with H2O (20 mL), dried over Na2SO4l filtered and concentrated. The residue was purified by préparative LC-MS to give racemic 7-(4methoxybenzyl)-6-methyl-3-((1R,2R,4S)-2-methyl-7-oxabicyclo[2.2.1]heptan-2yl)imidazo[1,5-a]pyrazin-8(7H)-one (40 mg, 27% yield).
114 1H NMR (CDCI3 400 MHz): δ 7.87 (s, 1H), 7.17 (d, J = 8.4 Hz, 2H), 6.84 (d, J = 8.8 Hz, 2H), 6.69 (s, 1H), 5.23-5.07 (m, 2H), 4.67 (d, J = 4.8 Hz, 2H), 3.78 (s. 3H), 2.71 (d, J= 12.0 Hz, 1H), 2.20 (s, 3H), 1.90-1.86 (m, 1H), 1.70-1.66 (m, 2H), 1.57 (s, 3H), 1.39-1.37 (m, 1H), 1.25-1.22 (m, 1H).
LC-MS: tR = 2.228 min (method 13), m/z = 380.2 [M + H]+.
Example 71:
N (S)-7-(4-methoxybenzyl)-6-methyl-3-(1-phenylethyI)imidazo[1,5-a]pyrazin-8(7H)-one:
Step 1: Te- a solution of (3-methoxy-5-methylpyrazin-2-yl)methanamine hydrochloride (300 ά rng, 1.58 mmol) and (S)-2-phenylpropanoic acid (261 mg, 1.74 mmol, 237 pL, 1.10 eq) in DCM (10 mL) was added triethylamine (400 mg, 3.95 mmol, 548 pL, 2.50 eq) and HATU (901 mg, 2.37 mmol, 1.50 eq). The mixture was stirred at 15°C for 12 hours. Water (50 mL) was added to the solution. The mixture was extracted with DCM (50 mL χ 2). The combined organic layers were washed with brine (50 mL), dried over Na2SO4t filtered and concentrated under reduced pressure. The residue was purified by flash silica gel chromatography (Eluent of 0-20% Ethyl acetate/petroleum ether). (S)-A/-((3-methoxy-5-methylpyrazin-2-yl)methyl)-2phenylpropanamide (450 mg, 1.56 mmol, 99% yield) was obtained.
'H NMR (CDCI3 400 MHz)- 5 7.81 (s, 1H), 7.24-7.37 (m, 5H), 6.74 (s, 1H), 4.37-4.52 (m, 2H), 3.92 (s, 3H), 3.67 (q, J = 7.1 Hz, 1 H), 2.40 (s, 3H), 1.56 (d, J = 7.2 Hz, 3H).
Step 2: To a solution of (S)-A/-((3-methoxy-5-methylpyrazin-2-yl)methyl)-2phenylpropanamide (450 mg, 1.58 mmol, 1 eq) in dioxane (10 mL) was added POCI3 (485 mg, 3.16 mmol, 294 pL, 2 eq). The mixture was stirred at 90°C for 12 hours. The reaction mixture was concentrated under reduced pressure to remove dioxane. The residue was quenched by addition H2O (50 mL) at 0°C, basified by addition saturated aqueous NaHCO3 (10 mL) and then extracted with EtOAc (50 mL x 2). The combined organic layers were washed with brine (50 mL), dried over Na2SO4t filtered and concentrated under reduced pressure. The residue was purified by flash silica gel chromatography (Eluent of 0-100%
115
Ethyl acetate/petroleum ether). (S)-6-methyl-3-(1-phenylethyl)imidazo[1,5-a]pyrazin-8-ol (128 mg, 505 pmol, 32% yieid).
Step 3: To a solution of (S)-6-methyl-3-(1-phenylethyl)imidazo[1,5-a]pyrazin-8-ol (128 mg, 505 pmol, 1 eq) and 1-(chloromethyl)-4-methoxybenzene (95 mg, 0.61 mmol, 83 pL, 1.20 eq) in DMF (10 mL) was added Cs2CO3 (329.29 mg, 1.01 mmol, 2 eq). The mixture was stirred at 60°C for 3 hours. The reaction mixture was concentrated under reduced pressure. The residue was purified by preparative LC-MS was further purified by SFC. (S)-7-(4methoxybenzyl)-6-methyl-3-(1-phenylethyl)imidazo[1,5-a]pyrazin-8(7H)-one (76.40 mg, 203 pmol. 40% yieid) was obtained 1H NMR (CDCI3 400 MHz): 5 7.98 (s, 1H), 7.17-7.31 (m, 5H), 7.12 (d, J = 8.4 Hz, 2H), 6.82 (d, J = 8.4 Hz, 2H), 6.46 (s, 1H), 5.10 (dd, J= 15.6 Hz, 2H), 4.26 (q, J = 7.2 Hz, 1H), 3.76 (s, 3H), 2.05 (s, 3H), 1.81 (d, J = 7.6 Hz, 3H).
LC-MS: tR = 2.218 min (method 17). m/z = 374.2 [M + H]+. SFC: tR= 1.641 min, ee% > 99%, [a]o 20 = -51.4 (c=0.11, MeOH).
Example 72:
N (R)-7-(4-methoxybenzyl)-6-methyl-3-(1-phenylethyl)imidazo[1,5-a]pyrazîn-8(7H)-one:
Step 1 : To a solution of (3-methoxy-5-methylpyrazin-2-yl)methanamine hydrochloride (200 mg, 1.05 mmol, 1 eq) and (R)-2-phenylpropanoic acid (190 mg, 1.27 mmol, 173 pL, 1.20 eq) m DCM (10 mL) was added triethylamine (267 mg, 2.64 mmol, 365 pL, 2.50 eq) and HATU (602 mg, 1.58 mmol, 1.50 eq). The mixture was stirred at 15°C for 12 hours. Water (50 mL) was added to the solution. The mixture was extracted with DCM (50 mL χ 2). The combined organic layers were washed with brine (50 mL), dried over Na2SO4, fïltered and concentrated under reduced pressure. The residue was purified by flash siltca gel chromatography (Eluent of 0-20% Ethyl acetate/petroleum ether). (R)-/V-((3-methoxy-5-methylpyrazin-2yl)methyl)-2-phenylpropanamide (300 mg, 1.02 mmol, 97% yieid) was obtained.
1H NMR (CDCI3400 MHz): 5 7.81 (s, 1H), 7.24-7.37 (m, 5H), 6.75 (s, 1H), 4.37-4.52 (m,
116
2H), 3.91 (s, 3H), 3.67 (q, J = 7.2 Hz, 1 H), 2.40 (s, 3H), 1.56 (d, J = 7.2 Hz, 3H).
Step 2: To a solution of (R)-A/-((3-methoxy-5-methylpyrazin-2-yl)methyl)-2phenylpropanamide (450 mg, 1.58 mmol, 1 eq) in dioxane (10 mL) was added POCI3 (727 mg, 4.74 mmol, 440 pL, 3 eq). The mixture was stirred at 90°C for 12 hours. The reaction mixture was concentrated under reduced pressure to remove dioxane. The residue was quenched by addition of H2O (50 mL) at 0°C basified by addition saturated aqueous NaHCO3 (10 mL) and then extracted with EtOAc (50 mL * 2). The combined organic layers were washed with brine (50 mL), dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by flash silica gel chromatography (Eluent of 0-100% Ethyl acetate/petroleum ether). (R)-6-methyl-3-(1-phenylethyl)imidazo[1,5a]pyrazin-8-ol (150 mg, 592 pmol, 37% yield) was obtained.
Step 3: To a solution of (R)-6-methyl-3-(1-phenylethyl)imidazo[1,5-a]pyrazin-8-ol (100 mg, 395 pmol, 1 eq) and 1-(chloromethyl)-4-methoxybenzene (74 mg, 474 pmol, 65 pL, 1.20 eq) in DMF (5 mL) was added Cs2CO3 (257 mg, 790 pmol, 2 eq). The mixture was stirred at 60°C for 3 hours. The reaction mixture was concentrated under reduced pressure. The residue was purified by préparative LC-MS. (R)-7-(4-methoxybenzyl)-6-methyl-3-(1phenylethyl)imidazo[1,5-a]pyrazin-8(7/-/)-one (140 mg, 95% yield) was obtained.
Ή NMR (CDCI3 400 MHz): 57.98 (s, 1H), 7.17-7.32 (m, 5H), 7.12 (d, J = 8.4 Hz, 2H), 6.82 (d, J = 8.4 Hz, 2H), 6.46 (s, 1 H), 5.10 (dd, J = 16.0 Hz, 2H), 4.26 (q, J = 7.2 Hz, 1 H), 3.76 (s, 3H), 2.05 (s, 3H), 1.81 (d, J = 6.8 Hz, 3H).
LC-MS: tR = 2.184 min (method 18), m/z = 374.1 [M + Hf. SFC: tR = 1.324 min, ee% 97.8%, [a]D Z0 = +50.7 (c=0.11, MeOH).
Example 73:
N
3-(1,4-dimethylpiperidin-4-yl)-7-(4-methoxybenzyl)-6-methylimidazo[1,5-a]pyrazin8(7 H)-o ne:
117
Step 1: To a solution of (3-methoxy-5-methylpyrazin-2-yl)methanamine hydrochloride (150 mg, 791 pmol) in DCM (5 mL) was added 1,4-dimethylpiperidine-4-carboxylic acid hydrochloride (169 mg, 870 pmol, 1.10 eq, HCl), triethylamine (240 mg, 2.37 mmol, 329 pL, 3 eq) and HATU (361 mg, 949 pmol, 1.20 eq). The mixture was stirred at 15°C for 16 hours. The mixture was concentrated. The residue was purified by preparative TLC (DCM/MeOH=10/1) to give N-((3-methoxy-5-methylpyrazin-2-yl)methyl)-1,4dimethylpiperidine-4-carboxamide (150 mg, 65% yield).
Step 2 To a solution of A/-((3-methoxy-5-methylpyrazin-2-yl)methyl)-1,4-dimethylpiperidine-
4-carboxamide (100 mg, 342 pmol, 1 eq) in dry dioxane (5 mL) was added POCI3 (105 mg, 684 pmol, 64 pL, 2 eq). The mixture was heated at 80°C for 4 hours. The mixture was cooled to 15°C and poured into water (5 mL). The mixture was adjusted to pH 8 by saturated aqueous NaHCO3 and concentrated. 10% MeOH in DCM (20 mL) was added to the residue and filtered, the filtrate was concentrated to give 3-(1,4-dimethylpiperidin-4-yl)-6methylimidazo[1,5-a]pyrazin-8-ol (90 mg).
Step 3 To a solution of 3-(1,4-dimethylpiperidin-4-yl)-6-methylimidazo[1,5-a]pyrazin-8-ol (60 mg, 230 pmol, 1 eq) in DMF (2 mL) was added 1-(chloromethyl)-4-methoxybenzene (54 mg, ± 346 pmoi, 47 pL, 1.50 eq) and Cs2CO3 (150 mg, 461 pmol, 2 eq). The mixture was heated at 60°C for 2 hours. The mixture was concentrated. DCM (20 mL) and H2O (10 mL) were added. The mixture was extracted with DCM (20 mL). The organic layer was washed with H2O (20 mL), dried over Na2SO4, filtered and concentrated. The residue was purified by preparative LC-MS to give 3-(1,4-dimethylpiperidin-4-yl)-7-(4-methoxybenzyl)-6methyIimidazo[1,5-a]pyrazin-8(7H)-one (20 mg, 23% yield).
1H NMR (CDCI3 400 MHz): 67.92 (s. 1 H), 7.17 (d, J = 8.8 Hz, 2H), 6.94 (s, 1 H), 6.84 (d, J = 8.8 Hz, 2H), 5.15 (s, 2H), 3.78 (s, 3H), 2.58-2.56 (m, 2H), 2.49-2.45 (m, 2H), 2.38-2.35 (m, 2H), 2.25 (s, 3H), 2.19 (s, 3H), 1.86-1.80 (m, 2H), 1.42 (s, 3H).
LC-MS: tR = 1.747 min (method 13), m/z = 381.2 [M + H]+.
Example 74:
118
Ο
3-(6-chIoro-2,3-dihydro-1H-inden-1 -yl)-7-(4-methoxybenzyl)-6-methylimidazo[1,5a]pyrazin-8(7H)-one:
Step 1 To a solution of (3-methoxy-5-methylpyrazin-2-yl)methanamine hydrochloride (200 mg, 1.05 mmol) and 6-chloro-2,3-dihydro-1H-indene-1-carboxylic acid (206 mg, 1.05 mmol, 1 eq) in DCM (5 mL) was added HATU (479 mg, 1.26 mmol, 1.20 eq) and DIPEA (407 mg, 3.15 mmol, 550 pL, 3 eq). The mixture was stirred at 18°C for 16 hours. The mixture washed with H2O (20 mL) and extracted with DCM (20 mL * 3). The combined organic was dried over Na2SO4 and concentrated under vacuum. 6-chloro-/V-((3-methoxy-5-methylpyrazin-2yl)methyl)-2,3-dihydro-1/7-indene-1-carboxamide (312 mg, 864 pmol, 82% yield) was obtained.
Step 2; To a solution of 6-chloro-/V-((3-methoxy-5-methylpyrazin-2-y!)methyl)-2,3-dihydro1H-indene-1-carboxamide (0.262 g, 1eq) in dioxane (10 mL) was added POCI3 (363 mg, 2.37 mmol, 220 pL, 3 eq). The mixture was stirred at 80°C for 3 hours. The mixture was quenched by H2O (20 mL) and adjusted pH > 7 by saturated aqueous NaHCO3. The mixture was extracted with DCM (25 mL * 3). The combined organic was dried over Na2SO4 and concentrated under vacuum. 3-(6-chloro-2,3-dihydro-1H-inden’1-yl)-6-methylimidazo[1,5a]pyrazin-8(7H)-one (236 mg) was obtained and directly used to next step.
Step 3: To a solution of 3-(6-chloro-2,3-dihydro-1/-/-inden-1-yl)-6-methylimidazo[1,5a]pyrazin-8(7H)-one (236 mg, 787 pmol, 1 eq) and 1-(chloromethyl)-4-methoxybenzene (148 mg, 945 pmol, 1.20 eq) in DMF (12 mL) was added Cs2CO3 (513 mg, 1.57 mmol, 2 eq). The mixture was stirred at 60°C for 2.5 hours. The mixture was concentrated under vacuum. The residue was quenched with H2O (15 mL) and extracted with DCM (20 mL * 3). The combined organic phases were dried over Na2SO4 and concentrated under vacuum. The residue was purified by preparative HPLC. 3-(6-chloro-2,3-dihydro-1/-/-inden-1-yl)-7-(4methoxybenzyl)-6-methylimidazo[1,5-a]pyrazin-8(7H)-one (99 mg, 237 pmol, 30% yield) was obtained.
119
Ή NMR (CDCI3 400 MHz): 5 7.93 (s, 1H), 7.30-7.18 (m, 4H), 6.98 (s, 1H), 6.88 (d, J =8.8 HZ, 2H), 6.64 (s, 1H), 5.18 (s, 2H), 4.71 (t, J =8.4 HZ 1H), 3.79 (s, 3H), 3.16-3.13 (m, 1H), 3.05-2.96 (m, 1H), 2.64-2.61 (m, 1H), 2.52-2.49 (m, 1H), 2.17 (s, 3H).
LC-MS: tR = 2.358 min (method 17), m/z = 420.1 [M + Hf.
Example 75:
O
7-(4-methoxybenzyl)-6-methyI-3-(3-methyl-5-oxopyrrolidin-3-yl)imidazo[1,5-a]pyrazin8(7H)-one:
Step 1: To a solution of ethyl 3-methyl-5-oxopyrrolidine-3-carboxyIate (200 mg, 1.17 mmol, 1 eq) in THF (4 mL) and H2O (2 mL) was added LiOHH2O (147.06 mg, 3.50 mmol, 3 eq). The mixture was stirred at 20°C for 16 hours. The mixture was acidified to pH=2 by 1 M HCl and extracted with ethyl acetate (20 mL χ 3). The combined organic layers were washed with H2O (20 mL), brine (20 mL), dried over Na2SO4, filtered and concentrated to give 3-methyl-5oxopyrrolidine-3-carboxylic acid (100 mg, 60% yield).
Step 2: To a cooled (0°C) solution of 3-methyl-5-oxopyrrolidine-3-carboxylic acid (100 mg, 0.7 mmol, 1 eq) in DCM (2 mL) was added oxalyl dichloride (98 mg, 768 pmol, 67 pL, 1.10 eq) and one drop of dry DMF was added. The mixture was stirred at 20°C for 1 hour.The colorless solution of 3-methyl-5-oxopyrrolidine-3-carbonyl chloride (112.89 mg) in DCM (2 mL) was directly used for the next step.
Step 3: To a cooled (0°C) solution of (3-methoxy-5-methylpyrazin-2-yl)methanamine (120 mg, 633 pmol, 1 eq, HCl) in dry DCM (3 mL) was added triethylamine (192 mg, 1.90 mmol, 263 pL, 3 eq) and a solution of 3-methyl-5-oxopyrrolidine-3-carbonyl chloride (112 mg, 696 pmol, 1.10 eq) in dry DCM (2 mL) dropwise. The mixture was stirred at 20°C for 1 hour. HZO (5 mL) was added and the mixture was extracted with DCM (20 mL χ 2). The combined organic layer was washed with H2O (20 mL), brine (20 mL), dried over Na2SO4, filtered and concentrated. The residue was purified by preparative TLC (DCM/MeOH=10/1) to give N18771
120 ((3-methoxy-5-methylpyrazin-2-yl)methyl)-3-nnethyl-5-oxopyrrolidine-3-carboxamide (75 mg, 42% yield).
Step 4: A solution of A/-((3-methoxy-5-methylpyrazin-2-yl)methyl)-3-methyl-5-oxopyrrolidine3-carboxamide (100 mg, 359 pmol, 1 eq) in Eaton's reagent (7.7 wt% phosphorus pentoxide solution in methanesulfonic acid) (2 mL) was heated at 60’C for 16 hours. The mixture was cooied to 15°C and poured into ice (5 g). The mixture was adjusted to pH=8 by 7 M NHa/MeOH and concentrated. 10% MeOH in DCM (20 mL) was added to the residue and filtered, the filtrate was concentrated to give 4-(8-hydroxy-6-methylimidazo[1,5-a]pyrazin-3yl)-4-methylpyrrolidin-2-one (100 mg).
Step 5: To a solution of 4-(8-hydroxy-6-methylimtdazo[1,5-a]pyrazin-3-yl)-4-methylpyrrolidin2-one (100 mg, 406 pmol, 1 eq) in DMF (5 mL) was added 1-(chloromethyl)-4methoxybenzene (76 mg, 487 pmol, 66 pL, 1.20 eq) and Cs2CO3 (265 mg, 812 pmol, 2 eq). The mixture was heated at 60°C for 2h. The mixture was concentrated. DCM (20 mL) and H2O (10 mL) was added. The mixture was extracted with DCM (20 mL). The organic layers were washed with H2O (20 mL), dried over Na2SO4, filtered and concentrated. The mixture was purified by préparative HPLC to give 7-(4-methoxybenzyl)-6-methyl-3-(3-methyl-5oxopyrrolidin-3-yl)imidazo[1,5-alpyrazin-8(7H)-one (40 mg, 27% yield).
1H NMR (CDCI3 400 MHz): 57.87 (s, 1H), 7.15 (d, J = 8.4 Hz, 2H), 6.84 (d, J= 8.4 Hz, 2H), 6.65 (s, 1H), 5.93(brs, 1H), 5.16 (s, 2H), 4.25 (d, J = 9.6 Hz, 1H), 3.77 (s, 3H), 3.53 (d, J = 10.4 Hz, 1H), 3.00 (d, J= 16.8 Hz, 1H), 2.57 (d, J = 16.4 Hz, 1H), 2.20 (s, 3H), 1.63 (s, 3H).
LC-MS: fR = 1.764 min (method 11), m/z = 367.1 [M + H]+.
Example 76:
O
3-(1-methoxy-2-methylpropan-2-yl)-7-(4-methoxybenzyl)-6-methylimidazo[1,5a]pyrazin-8(7H)-one:
Step 1: To a solution of 3-methoxy-2,2-dimethylpropanoic acid (115 mg, 870 pmol, 1 eq) in DCM (5 mL) was added oxalyl dichloride (121 mg, 957 pmol, 84 pL, 1.10 eq) at 0 °C,
121 followed by one drop of DMF. The mixture was stirred at 20 °C for 1 hour. The mixture was directly used to next step
Step 2: To a solution of 3-methoxy-2,2-dimethylpropanoyl chloride (150 mg, 791 pmol, 1 eq, HCl) and triethylamine (120 mg, 1.19 mmol, 164 pl_, 1.50 eq) in DCM (10mL) was added (3methoxy-5-methylpyrazin-2-yl)methanamine (131 mg, 870 pmol, 1.10 eq) in DCM (5mL).
The mixture was stirred at 20°C for 1 hour. The mixture was quenched with H2O (20 mL) and extracted with DCM (15 mL χ 3). The combined organic layers were dried over Na2SO4 and concentrated under vacuum. 3-methoxy-A/-((3-methoxy-5-methylpyrazin-2-yl)methyl)-2,2dimethylpropanamide (142 mg, 522 pmol, 66% yield) was obtained.
Step 3: To a solution of 3-methoxy-A/-((3-methoxy-5-methylpyrazin-2-yl)methyl)-2,2dimethylpropanamide (102 mg, 382 pmol, 1 eq) in dioxane (5 mL) was added POCI3 (117 mg, 763 pmol, 71 pL, 2 eq). The mixture was stirred at 80 °C for 2 hours. The mixture was quenched with water (20 mL) and extracted with DCM (20 mL χ 3). The combined organic layers were dried with Na2SO4 and concentrated under vacuum. 3-(1-methoxy-2methylpropan-2-yl)-6-methylimidazo[115-a]pyrazin-8(7/-/)-one (45 mg, 191 pmol, 50% yield) was obtained.
Step 4: To a solution of 3-(1-methoxy-2-methylpropan-2-yl)-6-methylimidazo[1,5-a]pyrazin8(7H)-one (62 mg, 264 pmol, 1 eq) and 1-(chloromethyl)-4-methoxybenzene (49.52 mg, 316 pmol, 43.06 pL, 1.20 eq) in DMF (5 mL) was added Cs2CO3 (171.72 mg, 527 pmol, 2 eq). The mixture was stirred at 60°C for 3 hours. The mixture washed with H2O (20 mL) and extracted with DCM (20 mL χ 3). The combined organic layers were dried over Na2SO4 and concentrated under vacuum. The residue was purified by preparative HPLC. 3-(1-methoxy2-methylpropan-2-yl)-7-(4-methoxybenzyl)-6-methylimidazo[1,5-a]pyrazin-8(7/-/)-one (25.15 mg, 71 pmol, 27% yield) was obtained.
ίΗ NMR (CDCI3 400 MHz): 5 7.91 (s, 1H), 7.20-7.17 (m, 3H), 6.86 (d, J=8.4 Hz, 2H), 5.15 (s, 2H), 3.79 (s, 3H), 3.59 (s, 2H), 3.35 (s, 3H), 2.18 (s, 3H), 1.52 (s, 6H).
LC-MS: (r = 2.050 min (method 13), m/z = 356.1 [M + H]+.
Example 77:
122
Ο
S-isoprOpyl-T-tA-methoxybenzyn-e-rnethylimidazotIjS-aJpyrazin-SiTHJ-one:
Step 1: To a cold (0°C) solution of (3-methoxy-5-methylpyrazin-2-yl)methanamine hydrochloride (150 mg. 791 pmol). Et3N (176 mg. 1.74 mmol, 241 pL, 2.20 eq) in anhydrous
DCM (5 mL) was added isobutyryl chloride (93 mg, 870 pmol, 91 pL, 1.10 eq). The solution was stirred at 0°C for 0.5h. The mixture was diluted with water (20 mL), extracted with DCM (20 mL χ 2). The organic layer was washed with brine (20 ml), dried over Na2SO4 and concentrated in vacuo. N-((3-methoxy-5-methylpyrazin-2-yl)methyl)isobutyramide (160 mg, 717 pmol, 91% yield) was obtained.
Step 2: To a solution of N-((3-methoxy-5-methylpyrazin-2-yl)methyl)isobutyramide (160 mg, 717 pmol. 1 eq) in dioxanedioxane (5 mL) was added POCI3 (220 mg, 1.43 mmol, 133 pL, 2 eq). The mixture was stirred at 90°C 2 hours. The mixture was concentrated in vacuo. 3isopropyl-8-methoxy-6-methylimidazo[1,5-a]pyrazine (130 mg, 633 pmol, 88% yield) was obtained.
Step 3: A solution of 3-isopropyl-8-methoxy-6-methylimidazo[1,5-a]pyrazine (130 mg, 633 pmol, 1 eq) in 2M HCI(aq) (4 mL) and dioxane (8 mL) was stirred at 90°C for 2 hours. The mixture was concentrated in vacuo. The residue was purified by silica gel chromatography (DCM:MeOH=10:1). 3-isopropyl-6-methylimidazo[1,5-a]pyrazin-8(7H)-one (120 mg, 628 pmol, 99% yield) was obtained.
Step 4: To a solution of 3-isopropyl-6-methylimidazo[1,5-a]pyrazin-8(7H)-one (120 mg, 628 pmol, 1 eq) in DMF (8 mL) was added 1-(chloromethyl)-4-methoxy-benzene (118 mg, 753 pmol, 103 pL, 1.20 eq) and Cs2CO3 (307 mg, 941 pmol, 1.50 eq). The mixture was stirred at 60°C for 16 hours. The mixture was filtered. The filtrate was purified by pre-HPLC (base). 3isopropyl-7-(4-methoxybenzyl)-6-methylimidazo[1,5-a]pyrazin-8(7H)-one (90 mg, 287 pmol,
46% yield) was obtained.
1H NMR (CDCI3400 MHz): 57.90 (s, 1H), 7.16 (d, J=8.4 Hz, 1H), 6.85 (d, J=8.4 Hz, 1H), 6.71 (s, 1H), 5.16 (s, 2H), 3.78 (s, 2H), 3.18-3.11 (m, 1H), 2.19 (s, 3H), 1.41-1.79 (d, J=7.2 Hz, 6H).
LC-MS: tR = 1.92 min (method 13), m/z = 312.1 [M + Hf.
123
Example 78:
6-methyl-7-((2-methylthiazol-4-yl)methyl)-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5a]pyrazin-8(7W)-one:
Into a vial was added 6-methyl-3-(tetrahydro-2/7-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one (30mg, 0.13 mmol), césium carbonate (84 mg, 0.26 mmol), 4-(chloromethyl)-2meîhylthiazole (23 mg, 0.15 mmol) and sodium iodide (23 mg, 0.15 mmol) in DMF (2 mL). The reaction was heated to 70°C, and stirred over night. The mixture was filtered and evaporated and subsequently chromatographed on silicagel to obtain the crude product.
Final purification on préparative LC-MS afforded 6-methyl-7-((2-methylthiazol-4-yl)methyl)-3(tetrahydrG-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one (3.9 mg, 0.013 mmol) in 10% yield.
1H NMR (600 MHz, DMSO-d6) δ 8.17 (s, 1H), 7.63 (m, 1H), 7.30 (m, 1H), 5.17 (s, 2H), 3.99 (t, J = 3.3 Hz, 1H). 3.97 (t, J= 3.1 Hz, 1H), 3.49 (m, 3H), 2.61 (s, 3H), 2.36 (d. J= 1.2 Hz, 3H), 1.83 (m, 4H).
LC-MS: tR = 0.39 min (method 5), m/z = 344.9 [M + H]+.
Example 79:
6-methyl-3-(tetrahydro-2H-pyran-4-yl)-7-(thiophen-3-ylmethyl)imidazo[1,5-a]pyrazin8(7H)-one:
124
Into a vial was added 6-methyl-3-(tetrahydro-2/7-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (3Qmg, 0.129 mmol), césium carbonate (84 mg, 0.26 mmol),3-(chloromethyl)thiophene (20 mg, 0.15 mmol) and sodium iodide (23 mg, 0.15 mmol) in DMF (2 mL). The reaction was heated to 70°C, and stirred over night. The mixture was filtered and evaporated and subsequently chromatographed on silicagel to obtain the crude product. Final purification on préparative LC-MS afforded 6-methyl-3-(tetrahydro-2H-pyran-4-yl)-7-(thiophen-3ylmethyl)imidazo[1,5-a]pyrazin-8(7H)-one (10 mg, 0.0324 mmol) in 25% yield.
Ή NMR (600 MHz, DMSO-d6) δ 8.21 (s, 1 H), 7.66 (m, 1 H), 7.53 (dd. J = 5.0, 2.9 Hz, 1 H), 7.35 (dq. J = 2.2, 1.0 Hz, 1H), 7.05 (dd, J= 5 0, 1.3 Hz, 1H), 5.17 (s, 2H). 3.98 (dt, J = 11.4, 3.4 Hz, 2H), 3.49 (m, 3H), 2.26 (d, J = 1.2 Hz, 3H), 1,84(m, 4H).
LC-MS: fR = 0.45 min (method 5), m/z = 329.9 [M + Hf.
Example 3ü:
O
6-methyl-3-(tetrahydro-2H-pyran-4-yl)-7-(thiazol-4-ylmethyI)imidazo[1,5-a]pyrazin8(7H)-one:
Into a vial was added 6-methyl-3-(tetrahydro-2/-f-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one (30mg, 0.129 mmol), césium carbonate (147 mg, 0.450 mmol), 4-(chloromethyl)thiazole hydrochloride (26 mg, 0.15 mmol) and sodium iodide (23 mg, 0.15 mmol) in DMF (2 mL). The reaction was heated to 70°C, and stirred over night. The mixture was filtered and evaporated and subsequently chromatographed on silicagel to obtain the crude product. Final purification on preparative LC-MS afforded 6-methyl-3-(tetrahydro-2/-/-pyran-4-yl)-7(thiazol-4-ylmethyl)imidazo[1,5-a]pyrazin-8(7H)-one (7 mg, 0.0153 mmol) in 12% yield.
1H NMR (600 MHz, DMSO-d6) δ 9.07 (d. J = 1.9 Hz, 1H), 8.12 (s, 1H), 7.63 (m, 1H), 7.57 (dd, J = 1.9, 0.9 Hz, 1 H), 5.27 (s, 2H), 3.97 (dt, J = 11.3, 3.3 Hz, 2H), 3.48 (m, 3H), 2.36 (d, J = 1.2 Hz. 3H), 1.84 (m, 4H).
LC-MS: fR = 0.34 min (method 5), m/z = 331.0 [M + Hf.
125
7-((3,5-dimethylisoxazol-4-yl)methyl)-6-methyl-3-(tetrahydro-2H-pyran-4yl)imidazo[1,5-a]pyrazin-8(7H)-one:
Into a vial was added 6-methyl-3-(tetrahydro-2/7-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one (25mg, 0.107 mmol), césium carbonate (70 mg, 0.21 mmol),4-(chloromethyl)-3,5dimethylisoxazole (19 mg, 0.129 mmol) and sodium iodide (19 mg, 0.129 mmol) in DMF (1.6 mL). The reaction was heated to 70°C, and stirred over night. The mixture was filtered and evaporated and subsequently chromatographed on silicagel to obtain the crude product. Final purification on préparative LC-MS afforded 7-((3,5-dimethylisoxazol-4-yl)methyl)-6methyl-3-(tetrahydro-2/7-pyran-4-yI)imidazo[1,5-a]pyrazin-8(7H)-one (11 mg, 0.024 mmol) in 23% yield.
1H NMR (600 MHz, DMSO-d6) δ 8.11 (s, 1H), 7.63 (m, 1H), 5.00 (s, 2H), 3.97 (dt, J = 11.3,
3.3 Hz, 2H), 3.46 (m, 3H), 2.27 (s, 3H), 2.24 (d, J = 1.2 Hz, 3H), 2.08 (s, 3H), 1.82 (dd, J = 7.8, 3.5 Hz, 4H).
LC-MS: tR = 0.38 min (method 5), mlz = 343.0 [M + H]*.
Example 82:
6-methyl-7-((5-methylisoxazol-3-yl)methyl)-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5a]pyrazin-8(7H)-one:
126
Into a vial was added 6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one (25mg, 0.107 mmol), césium carbonate (70 mg, 0.21 mmol),3-(chloromethyl)-5methylisoxazole (34 mg, 0.13 mmol, 50 %) and sodium iodide (19 mg, 0.13 mmol) in DMF (1.6 mL). The reaction was heated to 70°C, and stirred over night. The mixture was filtered and evaporated and subsequently chromatographed on silicagel to obtain the crude product. Final purification on préparative LC-MS afforded 6-methyl-7-((5-methylisoxazol-3-yl)methyl)3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (9 mg, 0.0194 mmol) in 18% yield.
’H NMR (600 MHz, DMSO-ds) δ 8.05 (s, 1H), 7.60 (m, 1H), 6.19 (q, J= 0.8 Hz, 1 H), 5.18 (s, 2H), 3.97 (dt, J= 11.3, 3.4 Hz, 2H), 3.45 (m, 3H), 2.37 (d, J= 0.9 Hz, 3H), 2.27 (d, J= 1.2 Hz, 3H), 1.86-1.79 (m, 4H).
LC-MS: tR = 0.38 min (method 5), m/z = 328.9 [M + Hf.
Example 83:
6-methyl-7-((3-methylisoxazol-5-yl)methyl)-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5a]pyrazin-8(7H)-one:
Into a vial was added 6-methyl-3-(tetrahydro-2/-i-pyran-4-yl)imtdazo[1,5-a]pyrazin-8(7/-/)-one (25mg, 0.107 mmol), césium carbonate (70 mg, 0.21 mmol), 5-(chloromethyl)-3methylisoxazole (17 mg, 0.13 mmol) and sodium iodide (19 mg, 0.13 mmol) in DMF (1.6 mL). The reaction was heated to 70°C, and stirred over night. The mixture was filtered and evaporated and subsequently chromatographed on silicagel to obtain the crude product. Final purification on preparative LC-MS afforded 6-methyl-7-((3-methylisoxazol-5-yl)methyl)3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one (14 mg, 0.0313 mmol) in 29 % yield.
1H NMR (600 MHz, DMSO-d6) δ 8.20 (s, 1 H), 7.70 (m, 1H), 6.31 (s, 1H), 5.29 (m, 2H), 3.98 (dt, J = 11.4, 3.5 Hz, 2H), 3.49 (m, 3H), 2.32 (d, J = 1.2 Hz, 3H), 2.19 (s, 3H), 1.85 (m, 4H).
127
LC-MS: tR = 0.37 min (method 5), m/z = 328.9 [M + Hf.
Example 84:
O
3-(2,6-dimethyltetrahydro-2H-pyran-4-yl)-7-(4-methoxybenzyl)-6-methylimidazo[1,5a]pyrazin-8(7H)-one:
Step 1: To a solution of (3-methoxy-5-methylpyrazin-2-yl)methanamine hydrochlorÎde (200 mg, 1.05 mmol, 1 eq) and 2,6-dimethyltetrahydro-2H-pyran-4-carboxylic acid (167 mg, 1.05 mmol, 1 eq) in DCM (10 mL) was added HATU (481 mg, 1.27 mmol, 1.20 eq) and DIPEA (409 mg, 3.16 mmol, 552 pL, 3 eq) .The mixture was stirred at 18°C for 16 hours. The mixture washed with H2O (20 mL) and extracted with DCM (20 mL * 3). The combined organic layers were dried over Na2SO4 and concentrated under vacuum. A/-((3-methoxy-5methylpyrazin-2-yl)methyl)-2,6-dimethyltetrahydro-2i!7-pyran-4-carboxamide (300 mg, 0.95 mmol, 90% yield) was obtained.
Step 2: To a solution of A/-((3-methoxy-5-methylpyrazin-2-yl)methyl)-2,6-dimethyltetrahydro2H-pyran-4-carboxamide (280 mg, 954 pmol, 1 eq) in dioxane (10 mL) was added POCI3 (293 mg, 1.91 mmol, 177 pL, 2 eq). The mixture was stirred at 80°C for 2 hours. The mixture washed with H2O (20 mL) and extracted with DCM (20 mL * 3). The combined organic layers were dried over Na2SO4 and concentrated under vacuum, 3-(2,6-dimethyltetrahydro2/7-pyran-4-yl)-6-methylimidazo[1,5-a]pyrazin-8(7/7)-one (249 mg) was obtained.
Step 3: To a solution of 3-(2,6-dimethyltetrahydro-2/7-pyran-4-yl)-6-methylimidazo[1,5a]pyrazin-8(7H)-one (200 mg, 765 pmol, 1 eq) and 1-(chloromethyl)-4-methoxybenzene (156 mg, 995 pmol, 135 pL, 1.30 eq) in DMF (10 mL) was added Cs2CO3 (500 mg, 1.53 mmol, 2 eq). The mixture was stirred at 60°C for 4 hours. The mixture was concentrated under vacuum. The mixture was washed with H2O (20 mL) and extracted with DCM (15 mL * 3). The combined organic layers were washed with H2O (40 mL * 3, brine, dried over Na2SO4 and concentrated under vacuum. The residue was purified by preparative LC-MS to
128 give 3-(2,6-dimethyltetrahydro-2/7-pyran-4-yl)-7-(4-methoxybenzyl)-6-methylimidazo[1,5a]pyrazin-8(7H)-one (48 mg, 126 pmol, 16% yield).
Ή NMR (CDCI3 400 MHz): δ 7.91 (s, 1H), 7.16 (d, J =8.4 HZ, 2H), 6.85 (d, J =8.4 HZ, 2H), 6.73 (s. 2H), 5.17 (s, 2H), 3.79 (s, 3H), 3.67-3.63 (m, 2H), 3.14-3.08 (m, 1H), 2.21 (s, 3H), 1.90-1.87 (m, 3H), 1.75-1.62 (m, 2H), 1.28 (d, 7=6.0 HZ, 6H).
LC-MS: iR = 2.133 min (method 17), m/z = 382.1 [M + H]*.
Example 85:
O
N
7-(cycIohexylmethy!)-6-methyl-3-propylimidazo[1,5-a]pyrazin-8(7H)-one:
Step 1: To a solution of 3-bromo-6-methylimidazo[1,5-a]pyrazin-8(7H)-one (1 g, 4.39 mmol, 1 eq) and Cs2CO3 (2.86 g, 8.78 mmol, 2 eq) in DMF (20 mL) was added (bromomethyl)cyciohexane (1.55 g, 8.78 mmol, 1.22 mL, 2 eq). The mixture was stirred at 60°C for 18 hour. The reaction mixture was filtered and the filtrate was concentrated. The crude mixture was purified by flash chromatography with petroleum etherethyl acetate = 5:1 - 3:1. 3-bromo-7-(cyclohexylmethyl)-6-methylimidazo[1,5-a]pyrazin-8(7/7)-one (1 g, 3.02 mmol, 69% yield) was obtained.
1H NMR (CDCI3, 400 MHz): δ 7.86 (s, 1 H), 6.80 (s, 1 H), 3.79 (d, 7 = 7.2 Hz, 2H), 2.29 (s, 3H), 1.75 -1.66 (m, 6H), 1.22 - 1.04 (m, 5H).
LC-MS: tR = 0.791 min (method 15), m/z = 325.9 [M + H]+.
Step 2: To a solution of 3-bromo-7-(cyclohexylmethyl)-6-methylimidazo[1,5-a]pyrazin-8(7/7)one (200 mg, 617 pmol, 1 eq) and (E)-4,4,5,5-tetramethyl-2-(prop-1-en-1-yl)-1,3,2dioxaboroîane (155 mg, 925 pmol, 1.50 eq) in dioxane (4 mL) and H2O (1 mL) was added Pd(dppf)CI2 (90 mg, 123 pmol, 0.20 eq) and Cs2CO3 (402 mg, 1.23 mmol, 2 eq) under a N2 atmosphère. The mixture was stirred at 90°C for 2 hours under microwave conditions. Water (50 mL) was added and the mixture was extracted with EtOAc (50 mL χ 3), the combined organic layers were washed with brine (20 mL), dried over Na2SO4 and concentrated. The
129 crude mixture was purified by flash chromatography with petroleum ethenethyl acetate= 1:1. (E)-7-(cyclohexylmethyl)-6-methyl-3-(prop-1 -en-1 -yl)imidazo[1,5-a]pyrazin-8(7/7)-one (150 mg, 504.59 pmol, 82% yield) was obtained.
Step 3: To a solution of (E)-7-(cyclohexylmethyl)-6-methyl-3-(prop-1-en-1-yl)imidazo[1,5a]pyrazin-8(7/7)-one (150 mg, 526 pmol, 1 eq) in EtOAc (30 mL) was added Pd-C (10%, 40 mg. wet) under N2 The suspension was degassed under vacuum and purged with H2 several times. The mixture was stirred under H2 (15 psi) at 25°C for 18 hours. The mixture was filtered and the residue was washed with EtOAc (20 mL * 2). The combined organic layers were concentrated. The residue was purified by préparative LC-MS to give 7(cyclohexy!methyl)-6-methyl-3-propylimidazo[1,5-a]pyrazin-8(7/-/)-one (95.5 mg, 321 pmol, 61% yield).
Ή NMR (400 MHz): δ 7.83 (s, 1 H). 6.66 (s, 1 H), 3.78 (d, J = 7.2 Hz, 2H), 2.81 (t, J = 7.6 Hz, 2H), 2.26 (s, 3H), 1.86-1.84 (m, 2H), 1.76- 1.67 (m, 6H), 1.19-1.17 (m, 3H), 1.05- 1.01 (m, 5H).
LC-MS: tR = 1.68 min (method 17), m/z = 288.3 [M + Hf.
Example 86:
O
OH
3-(2-hydroxypropan-2-yI)-7-(4-methoxybenzyl)-6-methylimidazo[1,5-a]pyrazin-8(7H)one:
Step 1: NaH (2.64 g, 66 mmol, 60% in minerai oil, 2.20 eq) was added to 2-hydroxy-2methylpropanoic acid (3.12 g, 30 mmol, 1 eq) in DMF (30 mL) at 0°C. The mixture was stirred a t 20°C for 30 mins. (bromomethyl)benzene (10.26 g, 60 mmol, 7.13 mL, 2 eq) was added to the reaction mixture at 20°C and stirred at 20°C for 16 hours. The mixture was quenched by H2O (30 mL) and adjusted pH=7 by HCl (1 M, aq). The mixture was extracted with ethyl acetate (30 mL χ 3). The combined organic layers were washed by H2O (20 mL) and brine. The residue was dried over Na2SO4 and concentrated under vacuum. 1H NMR
130 showed the compound was desired product. benzyl 2-(benzyloxy)-2-methylpropanoate (3.98 g, 14 mmol, 47% yield) was obtained.
1H NMR (CDCl3 400 MHz): 5 7.40-7.32 (m, 10H), 5.24 (s, 2H), 4.48 (s, 2H), 1.58 (s, 6H).
Step 2: To a solution of benzyl 2-(benzyloxy)-2-methylpropanoate (2 g, 7.03 mmol, 1 eq) in H2O (20 mL), THF (20 mL) and MeOH (20 mL) was added NaOH (1.12 g, 27.98 mmol. 3.98 eq). The mixture was stirred at 80°C for 1 hour. The mixture was adjusted pH=2 by aq. HCl (1 M) and extracted with DCM (10 mL χ 3). The combined organic layers were concentrated under vacuum. The residue was washed with aq. NaOH (1 M, 5 mL) and extracted with DCM (15 mL x 3). The aqueous solution was adjusted pH=2 by aq. HCl (1 M, aq) and extracted with DCM (10 mL χ 3). The combined organic layers were washed with H2O (15 mL χ 2) and brine. The mixture was dried over Na2SO4 and concentrated under vacuum. 2(benzyloxy)-2-methylpropanoic acid (1.36 g, 7 mmol, 100% yield) was obtained.
Step 3: To a solution of 2-(benzyloxy)-2-methylpropanoic acid (500 mg, 2.64 mmol, 1 eq, HCl) in DCM (10 mL) was added DIPEA (1.02 g, 7.92 mmol, 1.38 mL, 3 eq) .The mixture was added (3-methoxy-5-methylpyrazin-2-yl)methanamine hydrochloride (513 mg, 2.64 mmol, 1 eq) and HATU (1.20 g, 3.17 mmol, 1.20 eq). The mixture was stirred at 18 °C for 16 hours. The mixture washed with H2O (20 mL) and extracted with DCM (20 mL χ 3). The combined organic layers were dried over Na2SO4 and concentrated under vacuum. 2(benzyloxy)-N-((3-methoxy-5-methylpyrazin-2-yl)methyl)-2-methylpropanamîde (617 mg, 1.75 mmol, 66% yield) was obtained.
Step 4: To a solution of 2-(benzyloxy)-A/-((3-methoxy-5-methylpyrazin-2-yl)methyl)-2methylpropanamide (1.40 g, 4.25 mmol, 1 eq) in dioxane (20 mL) was added POCI3 (1.30 g, 8.50 mmol, 790 pL, 2 eq) .The mixture was stirred at 80°C for 2 hours. The mixture was quenched with H2O (15 mL) and adjusted pH >7 by saturated aqueous NaHCO3. The mixture was extracted with DCM (20 mL χ 3). The combined organic layers were washed with brine, dried over Na2SO4 and concentrated under vacuum. 3-(2-(benzyloxy)propan-2yl)-6-methylimidazo[1,5-a]pyrazin-8(7/-/)-one (375 mg, 1.26 mmol, 30% yield) was obtained.
Step 5: To a solution of 3-(2-(benzyloxy)propan-2-yl)-6-methylimidazo[1,5-a]pyrazin-8(7/-/)one (264 mg, 888 pmol, 1 eq) in DMF (10 mL) was added Cs2CO3 (579 mg, T.78 mmol, 2 eq) and 1-(chloromethyl)-4-methoxybenzene (180.76 mg, 1.15 mmol, 1578 pL, 1.30 eq). The mixture was stirred at 60°C for 4 hours. The mixture was concentrated under vacuum. The mixture was washed with H2O (25 mL) and extracted with DCM (20mL). The combined organic layers were dried over Na2SO4 and concentrated under vacuum. 3-(218771
131 (benzyloxy)propan-2-yl)-7-(4-methoxybenzyl)-6-methylimidazo[1,5-a]pyrazin-8(7/7)-one (445 mg, 998 pmol, 64% yield) was obtained.
Step 6: To a solution of 3-(2-(benzyloxy)propan-2-yl)-7-(4-methoxybenzyl)-6methylimidazo[1,5-a]pyrazin-8(7H)-one (345 mg, 826 pmol, 1 eq) in MeOH (60 mL) was added Pd/C (10%, wet) (40 mg). The mixture was stirred at pressure of H2 (30 psi). The mixture was stirred at 18°C for 8 hours The mixture was filtered. The filtered solution was concentrated under vacuum. The residue was purified by TLC (petroleum ethenethyl acetate=1.1) 3-(2-hydroxypropan-2-yi)-7-(4-methoxybenzyl)-6-methylimidazo[1,5-a]pyrazin8(7H)-one (98 mg, 292 pmol, 35% yield) was obtained 1H NMR (CDCI3 400 MHz): 57.86 (s, 1H), 7.47 (s, 1H), 7.17 (d, J =12 Hz. 2H), 6.85 (d, J =8.4 Hz, 2H), 5.17 (s, 2H), 3.79 (s, 3H), 2.216-2.192 (m, 4H), 1.76 (s, 3H).
LC-MS: tR = 1.906 min (method 13), mlz = 328.2 [M + H]+.
Example 87:
N
3-(2-fluoropropan-2-yl)-7-(4-methoxybenzyl)-6-methylimidazo[1,5-a]pyrazin-8(7H)-one:
To a solution of 3-(2-hydroxypropan-2-yl)-7-(4-methoxybenzyl)-6-methylimidazo[1,5a]pyrazin-8(7/-/)-one (75 mg, 229.09 pmol, 1 eq) in DCM (10 ml) was added DAST (40.6 mg, 252 pmol, 33 pL, 1.10 eq) at -78°C. The mixture was stirred at 18°C for 2 hours. The mixture was quenched with H2O (10mL) and extracted with DCM (15 mL χ 3). The combined organic layers were dried over Na2SO4 and concentrated under vacuum. The residue was purified with TLC (petroleum ethecethyl acetate=1:1). 3-(2-fluoropropan-2-yl)-7-(4methoxybenzyl)-6-methylimidazo[1,5-a]pyrazin-8(7H)-one (68 mg, 206 pmol, 64% yield) was obtained.
1H NMR (CDCI3 400 MHz): 5 7.89 (s, 1H), 7.19-7.16 (m, 3H), 6.86 (d, J =8.4 Hz, 2H), 5.18 (s, 2H), 3.79 (s, 3H), 2.20 (s, 3H), 1.91 (s, 3H), 1.86 (s, 3H).
LC-MS: fR = 1.906 min (method 13), mlz = 328.2 [M + H]+.
132
Example 88:
Ο
Ο
7-(4-methoxybenzyl)-6-methyl-3-(7-oxoazepan-4-yI)imidazo[1,5-a]pyrazin-8(7H)-one:
Step 1: To a solution of (3-methoxy-5-methylpyrazin-2-yl)methanamine hydrochloride (500 mg, 2.64 mmol, 1 eq) and 7-oxoazepane-4-carboxylic acid (456 mg, 2.90 mmol, 1.10 eq) in DCM (45 mL) was added HATU (1 20 g, 3.17 mmol, 1.20 eq) and DIPEA (1.02 g, 7.92 mmol, 1.38 mL, 3 eq). The mixture was stirred at 18 °C for 16 hours. The mixture was quenched with H2O (30 mL) and extracted with DCM (25 mL χ 3). The combined organic layers were dried over Na2SO/, and concentrated under vacuum. N-((3-methoxy-5 methylpyrazin-2-yl)methyl)-7-oxoazepane-4-carboxamide (493 mg, 1.58 mmol, 60% yieid) was obtained.
Step 2: A/-((3-methoxy-5-methylpyrazin-2-yl)methyl)-7-oxoazepane-4-carboxamide (463 mg,
1.58 mmol, 1 eq) was added to Eaton's reagent (7.7 wt% phosphorus pentoxide solution in methanesulfonic acid) (3.04 g, 12.77 mmol, 2 mL, 8.08 eq). The mixture was stirred at 60°C for 7 hours. The mixture was added to ice (30 g). The mixture was adjusted pH>7 by NH3 (MeOH). The mixture was concentrated under vacuum. The residue was washed with DCM MeOH =10:1 The mixture was filtered. The filtered solution was concentrated under vacuum. 6-methyl-3-(7-oxoazepan-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one (45 mg, 165.83 pmol, 11% yieid) was obtained.
1H NMR (MeOD 400 MHz): 5 7.77 (s, 1H), 7.23 (s, 2H), 3.49-3.39 (m, 3H), 2.83-2.79 (m, 2H), 2.55-2.51 (m, 1H), 2.19 (s, 3H), 2.11-2.09 (m, 2H), 1.93-1.86 (m, 2H).
Step 3: To a solution of 6-methyl-3-(7-oxoazepan-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one (45 mg, 173 pmol, 1 eq) and 1-(chloromethyl)-4-methoxybenzene (32 mg, 207 pmol, 28 pL, 1.20 eq) in DMF (3 mL) was added Cs2CO3 (113 mg, 346 pmol, 2 eq). The mixture was stirred at 60°C for 2 hours. The mixture was washed with H2O (10 mL) and extracted with DCM (15 mL χ 3). The combined organic layers were washed with water (30 mL χ 3), dried
133 over Na2SO4 and concentrated under vacuum. The residue was purified by TLC (DCM:MeOH=10:1). 7-(4-methoxybenzyl)-6-methyl-3-(7-oxoazepan-4-yl)imidazo[1,5a]pyrazin-8(7H)-one (12 mg, 32 pmol, 18% yield) was obtained.
1H NMR (CDCI3 400 MHz): 5 7.89 (s, 1H), 7.15 (d, J =8.8 HZ, 2H), 6.84 (d, J =8.4 HZ, 2H), 6.70 (s, 1H), 6.36 (brs, 1H), 5.16 (s, 2H). 5.16 (s, 2H), 3.77 (s, 3H),3.62-3.49 (m, 1H), 3.423.30 (m. 1H). 3 20-3 10 (m. 1H). 2 77-2.72 (m. 1H), 2.61-2 55 (m, 1H). 2.21 (s. 3H). 2.102.01 (m, 4H).
LC-MS: fR = 1.748 min (method 13), m/z = 381.2 [M + H]*.
Example 89:
O
7-(4-methoxybenzyl)-6-methyl-3-(5-methyltetrahydrofuran-3-yl)imidazo[1,5-a]pyrazïn8(7H)-one:
Step 1: To a solution of (3-methoxy-5-methylpyrazin-2-yl)methanamine (200 mg, 1.05 mmol, 1 eq, HCI) and 5-methyltetrahydrofuran-3-carboxylic acid (137 mg, 1.05 mmol, 1 eq) in DCM (10 mL) was added HATU (481 mg, 1.27 mmol, 1.20 eq) and DIPEA (409 mg, 3.16 mmol, 553 pL, 3 eq). The mixture was stirred at 18°C for 16 hours. The mixture washed with H2O (20 mL) and extracted with DCM (20 mL * 3). The combined organic layers were dried over Na2SO< and concentrated under vacuum. A/-((3-methoxy-5-methylpyrazin-2-yl)methyl)-5methyltetrahydrofuran-3-carboxamide (211 mg, 795 pmol, 76% yield) was obtained.
Step 2: To a solution of /V-((3-methoxy-5-methylpyrazin-2-yl)methyl)-5methyltetrahydrofuran-3-carboxamide (191 mg, 720 pmol, 1 eq) in dioxane (5 mL) was added POCI3 (221 mg, 1.44 mmol, 134 pL, 2 eq) .The mixture was stirred at 80°C for 3 hours. The mixture washed with H2O (20 mL) and extracted with DCM (20 mL χ 3). The combined organic layers were dried over Na2SO4 and concentrated under vacuum. 6methyl-3-(5-methyltetrahydrofuran-3-yl)imidazo[1,5-a]pyrazin-8(7H)-one (167 mg) was obtained.
134
Step 3: To a solution of 6-methyl-3-(5-methyltetrahydrofuran-3-yl)imidazo[1,5-a]pyrazin8(7H)-one (138 mg, 592 pmol, 1 eq) and 1-(chloromethyl)-4-methoxybenzene (120 mg, 769 pmol, 1.30 eq) in DMF (10 mL) was added Cs2CO3 (386 mg, 1.18 mmol, 2 eq). The mixture was stirred at 60°C for 4 hours. The mixture was concentrated under vacuum. The mixture was washed with H2O (20 mL) and extracted with DCM (15 mL χ 3). The combined organic layers were washed with H2O (40 mL χ 3, brine, dried over Na2SO4 and concentrated under vacuum. The residue was purified by pre-HPLC(base). 7-(4-methoxybenzyl)-6-methyl-3-(5methyltetrahydrofuran-3-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one (10 mg, 28 pmol, 5% yield) was obtained.
1H NMR (CDCI3400 MHz): <5 7.90 (s, 1H), 7.16 (d, J=8.4 HZ, 2H), 6.87-6.82 (m, 3H), 5.17 (s, 2H), 4.19-4.14 (m, 3H), 3.79-3.71 (m, 4H), 2.54-2.47 (m, 1H), 2.20 (s, 3H), 2.04-1.96 (m, 1H), 1.40 (s, J =6.0 HZ, 3H).
LC-MS: fR = 2.036 min (method 13), mlz = 354.2 [M + Hf.
Example 90:
O
7-(4-methoxybenzyl)-6-methyl-3-(1-(4-methylthiazol-2-y[)ethyl)imidazo[1,5-a]pyrazin8(7H)-one:
Step 1: To a solution of (3-methoxy-5-methylpyrazin-2-yl)methanamine hydrochloride(150 mg, 791 pmol, 1 eq) in dry DMF (5 mL) was added triethylamine (240 mg, 2.37 mmol, 329 pL, 3 eq), sodium 2-(4-methylthiazol-2-yl)propanoate (153 mg, 791 pmol, 1 eq) and HATU (361 mg, 949 pmol, 1.20 eq). The mixture was stirred at 15°C for 16 hours. The mixture was concentrated. H2O (5 mL) was added and the mixture was extracted with DCM (20 mL χ 2). The combined organic layer was washed with H2O (20 mL), brine (20 mL), dried over Na2SO4, filtered and concentrated. The residue was purified by flash chromatography on silica geî (0%~50% ethyl acetate in petroleum ether) to give A/-((3-methoxy-5-methylpyrazin2-yl)methyl)-2-(4-methylthiazol-2-yl)propanamide (210 mg. 87% yield).
135
Step 2: To a solution of /V-((3-methoxy-5-methylpyrazin-2-yl)methyl)-2-(4-methylthiazol-2yl)propanamide (200 mg, 653 pmol, 1 eq) in dry dioxane (5 mL) was added POCI3 (200 mg, 1.31 mmol, 121 pL, 2 eq). The mixture was heated at 80°C for 4 hours. The mixture was cooled to 15°C and poured into water (5 mL). The mixture was adjusted to pH 8 by saturated aqueous NaHCO3 and extracted with DCM (20 mL χ 2). The combined organics were washed with H2O (20 mL), brine (20 mL), dried over Na2SO4, filtered and concentrated to give 6-methyl-3-(1-(4-methylthiazol-2-yl)ethyl)imidazo[1,5-a]pyrazin-8-ol (160 mg).
Step 3: To a solution of 6-methyl-3-(1-(4-methylthiazol-2-yl)ethyl)imidazo[1,5-a]pyrazin-8-ol (180 mg, 656 pmol, 1 eq) in DMF (5 mL) was added 1-(chloromethyl)-4-methoxy-benzene (123 mg, 787 pmol, 107 pL, 1.20 eq) and Cs2CO3 (428 mg, 1.31 mmol, 2 eq). The mixture was heated at 60°C for 2h. The mixture was concentrated. DCM (20 mL) and H2O (10 mL) was added. The mixture was extracted with DCM (20 mL). The organic layer was washed with H2O (20 mL), dried over Na2SO4, filtered and concentrated. The residue was purified by préparative LC-MS to give 7-(4-methoxybenzyl)-6-methyl-3-(1-(4-methylthiazol-2yl)ethyl)imidazo[1,5-a]pyrazin-8(7/7)-one (30 mg, 12% yield).
’H NMR (CDCI3400 MHz): δ 7.95 (s, 1H), 7.13 (d, J = 8.4 Hz, 2H), 6.91 (s, 1H), 6.82 (d, J =
8.4 Hz, 2H), 6.79 (s, 1H), 5.19-5.06 (m, 2H), 4.76 (q, J = 7.2 Hz, 1H), 3.76 (s, 3H), 2.41 (s, 3H), 2.14 (s, 3H), 1.92 (d, J = 7.2 Hz, 1H).
LC-MS: tR = 2.532 min (method 11), m/z = 395.1 [M + H]+.
Example 91:
3-(7-(4-methoxybenzyl}-6-methyl-8-oxo-7,8-dîhydroimidazo[1,5-a]pyrazin-3-yl)-3methylpyrrolidine-1-sulfonamide;
Step 1: To a solution of (3-methoxy-5-methylpyrazin-2-yl)methanamine (200 mg, 1.05 mmol, 1 eq, HCl) and 1-((benzyloxy)carbonyl)-3-methylpyrrolidine-3-carboxylic acid (304 mg, 1.16 mmol, 1.10 eq) in DCM (10 mL) was added HATU (479 mg, 1.26 mmol, 1.20 eq) and DIPEA (407 mg, 3.15 mmol, 550 pL, 3 eq). The mixture was stirred at 18°C for 16 hours. The
136 mixture was quenched with H2O (30 mL) and extracted with DCM (25 mL * 3). The combined organic layers were dried over Na2SO4 and concentrated under vacuum. Benzyl 3-(((3-methoxy-5-methylpyrazin-2-yl)methyl)carbamoyl)-3-methylpyrrolidine-1-carboxylate (420 mg, 1.01 mmol, 96% yield) was obtained.
Step 2: To a solution of benzyl 3-(((3-methoxy-5-methylpyrazin-2-yl)methyl)carbamoyl)-3methylpyrrolidine-1-carboxylate (390 mg, 979 pmol. 1 eq) in dioxane (15 mL) was added POCI3 (300 mg, 1.96 mmol, 182 pL, 2 eq). The mixture was stirred at 80°C for 3 hours. The solution was quenched with H2O (20 mL) and extracted with DCM (20 mL χ 3). The combined organic layers were dried over Na2SO4 and concentrated under vacuum. Benzyl 3-methyl-3-(6-methyl-8-oxo-7,8-dihydroimidazo[1,5-a]pyrazin-3-yl)pyrrolidine-1-carboxylate (170 mg, 423 pmol, 43% yield) was obtained.
Step 3: To a solution of benzyl 3-methyl-3-(6-methyl-8-oxo-7,8-dihydroimidazo[1,5-a]pyrazin3-yl)pyrrolidine-1-carboxylate (290 mg, 791 pmol, 1 eq) and di-tert-butyl dicarbonate (207 mg, 950 pmol, 218 pL, 1.20 eq) in MeOH (200 mL) was added Pd/C (10%, wet) (140 mg). The suspension was degassed under vacuum and purged with H2 several times. The mixture was stirred under H2 (30 psi) at 25°C for 5 hours. The mixture was filtered. The filtered solution was concentrated under vacuum, tert-butyl 3-methyl-3-(6-methyl-8-oxo-7,8dihydroirnidazo[1.5-a]pyrazin-3-yl)pyrrolidine-1-carboxylate (204 mg, 614 pmol, 78% yield) was obtained.
Step 4: To a solution of tert-butyl 3-methyl-3-(6-methyl-8-oxo-7,8-dihydroimidazo[1,5a]pyrazin-3-yl)pyrrolidine-1-carboxylate (274 mg, 824 pmol, 1 eq) and 1-(chloromethyl)-4methoxybenzene (155 mg, 989 pmol, 135 pL, 1.20 eq) in DMF (15 mL) was added Cs2CO3 (537 mg, 1.65 mmol, 2 eq). The mixture was stirred at 80°C for 14 hours. The mixture was concentrated under vacuum. The mixture was washed with H2O (15 mL) and extracted with DCM (15 mL χ 3). The combined organic layers were washed with H2O (30 mL χ 2), dried over Na2SO4 and concentrated under vacuum, tert-butyl 3-(7-(4-methoxybenzyl)-6-methyl-8oxo-7,8-dihydroimidazo[1,5-a]pyrazin-3-yl)-3-methylpyrrolidine-1-carboxylate (291 mg, 537 pmol, 65% yield) was obtained.
Step 5: To a solution of tert-butyl 3-(7-(4-methoxybenzyi)-6-methyl-8-oxo-7,8dihydroimidazo[1,5-a]pyrazin-3-yl)-3-methylpyrrolidine-1-carboxylate (288 mg, 636 pmol, 1 eq) in ethyl acetate (4 mL) was added HCI/EtOAc (4 M, 4 mL, 25 eq). The mixture was stirred at 18°C for 4 hours. The mixture was concentrated under vacuum. 7-(4methoxybenzyl)-6-methyl-3-(3-methylpyrrolidin-3-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one (247. mg, crude, HCl) was obtained. The product was directly used next step.
137
Step 6: To a solution of 7-(4-methoxybenzyl)-6-methyl-3-(3-methylpyrrolidin-3-yl)imidazo[1,5a]pyrazin-8(7H)-one (250 mg, 709 pmol, 1 eq) and sulfuric diamide (82 mg, 851 pmol, 51 pL, 1.20 eq) in dioxane (20 mL) was added DIPEA (183 mg, 1.42 mmol, 248 pL, 2 eq). The mixture was stirred at 100°C for 24 hours. The mixture was quenched with H2O (20 mL) and extracted with DCM (20 mL χ 3). The combined organic layers were dried over Na2SO4 and concentrated under vacuum. The residue was purified pre-HPLC (base). 3-(7-(4methoxybenzyl)-6-methyl-8-oxo-7,8-dihydroimidazo[1,5-a]pyrazin-3-yl)-3-methylpyrrolidine1-sulfonamide (14 mg. 32 pmol. 5% yield) was obtained.
1H NMR (CDCI3 400 MHz): 5 7.91 (s. 1H), 7.16 (d, J =8.4 HZ. 2H). 7.85 (s, 1H), 7.18 (d, J =8.0 HZ, 2H), 6.88-6.82 (m, 3H), 5.17 (s, 2H), 4.79 (m, 1H), 4.30 (d, J =10.4 HZ, 1H), 3.79 (s, 3H), 3.52-3.47 (m, 2H), 3.26-3.20 (m. 1H), 2.73-2.64 (m, 1H), 2.23-2.17 (m, 5H), 1.65-
1.59 (m, 4H).
LC-MS: fR = 2.055 min (method 13), mlz = 432.2 [M + Hf.
Example 92:
6-(cyclopentylmethyl)-7-(4-methoxybenzyl)-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5a]pyrazin-8(7H)-one:
6-(bromomethyl)-7-(4-methoxybenzyl)-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin8(7H)-one (250 mg, 0.439 mmol) was dissolved in THF (20 ml), at -78°C.
cyclopentylmagnesium bromide (0.9 ml, 1.8 mmol, 2 molar in ether) was added and the reaction was allowed to warm to room température ovemight. Cyclopentylmagnesium bromide (0.9 ml, 1.8 mmol, 2 molar in ether) was added. After 1 hour the reaction was warmed to room température. After two hours, the reaction mixture was quenched with sat. NH4CI, extracted with AcOEt and organics were washed with brine. The combined organics layers were dried with ^28()4, filtered and concentrated. The mixture was purified via préparative LC-MSand 6-(cyciopentylmethyl)-7-(4-methoxybenzyl)-3-(tetrahydro-2H-pyran-418771
138 yl)imidazo[1,5-a]pyrazin-8(7/-/)-one (26 mg, 0.049 mmol) was isolated in 11% yield, as the TFA sait.
Ή NMR (500 MHz, Chloroform-d) δ 13.26 (bs, 1H), 8.14 (s, 1H), 7.12 (d, 8.2 Hz, 2H),
6.88 (m, 3H), 5.21 (s, 2H), 4.16 (d, J = 11.7 Hz, 2H). 3.80 (s, 3H), 3.60 (t, J = 11.8 Hz, 2H), 3.46 (t, J = 12.4 Hz, 1 H), 2.74 (s, 1 H). 2.57 (d, J = 7.0 Hz, 2H), 2.25 - 2.07 (m, 2H), 1.90 (m, 4H). 1 65 (m. 4H). 1.23 (dt. 13 2. 7 1 Hz. 2H)
LC-MS: iR = 0.69 min (method 5). mlz = 422.0 [M + H]+.
Example 93:
O
7-(4-methoxybenzyl)-6-methyl-3-morpholînoîmidazo[1,5-a]pyrazin-8(7H)-one:
To a mixture of 3-bromo-7-(4-methoxybenzyl)-6-methylimidazo[1,5-a]pyrazin-8(7/-/)-one (300 mg, 0.86 mmol) and morpholine (150 mg, 1.72 mmol) in DMSO (5 mL) were added CsF (261 mg, 1.72 mmol) and K2CO3 (238 mg, 1.72 mmol). The mixture was stirred at 100°C for 24 hours. The mixture was diluted with water (20 mL) and extracted with DCM (10 mL χ 3). The combine organic layers were washed with water (10 mL χ 2); dried over Na2SO4and evaporated under vacuum. The residue was purified by preparative TLC (ethyl acetate) to give 7-(4-methoxybenzyl)-6-methyl-3-morpholinoimidazo[1,5-a]pyrazin-8(7/-/)-one (18 mg, 6% yield).
1H NMR (CDCI3. 400 MHz): δ 7.76 (s, 1H), 7.16 (d, J = 8.8 Hz, 2H), 6.85 (d, J = 8.8 Hz, 2H), 6.63 (s, 1H), 5.15 (s, 2H), 3.89 (t, J = 4.8 Hz, 4H), 3.79 (s, 3H), 3.21 (t, J = 4.8 Hz, 4H), 2.18 (s, 3H).
LC-MS: tR = 2.03 min (method 13), m/z = 355.1 [M + H]+.
Example 94:
139
Ο
NH
7-(4-methoxybenzyl)-6-methyl-3-((tetrahydrofuran-3-yl)amino)imidazo[1,5-a]pyrazin8{7H)-one:
3-bromo-7-(4-methoxybenzyl)-6-methylimidazoE1,5-a]pyrazin-8(7/-/)-one (60 mg, 0.172 mmol) and tetrahydrofuran-3-amine (0.04 ml, 0.465 mmol) were mixed in NMP (2 mL) and DIPEA (0.23 ml, 1.317 mmol).
The reaction was heated for 4 hours at 250°C in the microwave oven.
The reaction was purified on silica gel, via préparative LC-MS, and préparative TLC (10% EtOH in ethyl acetate) to give 7-(4-methoxybenzyl)-6-methyl-3-((tetrahydrofuran-3yl)amino)imidazo[1,5-a]pyrazin-8(7H)-one (2 mg, 0.005 mmol) in 3% yield.
1H NMR (600 MHz, Dimehtylsulfoxide-d6) δ 8.50 (m, NH), 7.68 (s, 1H), 7.31 (s, 1H) 7.22 (d, J= 7.1 Hz, 2H), 6.88 (d, J = 7.1 Hz. 2H), 4.87 (m, 1H), 4.35 (d, J = 14 Hz, 2H), 4.11 (m, 1H), 4.02 (m, 1H), 3.92 (m, 1H), 3.86 (m, 1H), 3.71 (s, 3H), 2.60 (m, 1H), 2.5 (m, 1H) 2.31 (s, 3H).
LC-MS: tR = 0.54 min (method 19), m/z = 355.2 [M + H]*.
Example 95:
O
(/?)-7-(4-methoxybenzyl)-6-methyl-3-(3-methylmorpholino)imidazo['lI5-a]pyrazin-8(7W)one:
3-bromo-7-(4-methoxybenzyl)-6-methylimidazo[1,5-a]pyrazin-8(7H)-one (80 mg, 0,23 mmol) and (R)-3-methylmorpholine (34.7 mg, 0.039 ml, 0.343 mmol) were mixed in NMP (2.0 mL) and DIPEA (0.2 ml, 1.1 mmol) was added.
140
The reaction was heated for 6.5 hours at 250°C in the mîcrowave oven.
The reaction was purified directly by préparative LC-MSto give (R)-7-(4-methoxybenzyl)-6methyl-3-(3-methylmorpholino)imidazo[1,5-a]pyrazin-8(7H)-one (10 mg, 0.024 mmol) in 10% yield.
’H NMR (500 MHz. Chloroform-d) δ 8.00 (s. 1 H), 7.18 (d. J = 7.1 Hz. 2H), 6.90 (d, J = 7.1 Hz,. 2H), 6.79 (s, 1H), 5.23 (d, J = 14.0 Hz, 1H), 5.13 (d, J = 15.7 Hz, 1 H), 3.94 (m, 1H), 3.85 (m. 1 H), 3.81 (s, 3H), 3.60 (m, 1 H), 3.48 (dd, J = 11.7, 7.9 Hz. 1 H), 3.32 (t. J = 10.3 Hz. 1 H), 3.22 (d, J = 12.2 Hz. 1H), 2.28 (d, J= 1.6 Hz, 3H), 1.29 (td, J = 7.1, 1.6 Hz, 1H), 1.00 (dd, J = 6.4, 1.5 Hz, 3H).
LC-MS: tR = 0.65 min (method 7), mlz = 369.1 [M + H]+.
Example 96:
O
(S)-7-(4-methoxybenzyl)-6-methyl-3-(3-methyImorpholino)imidazo[1,5-a]pyrazin-8(7H)one:
3-bromo-7-(4-methoxybenzyl)-6-methylimidazo[1,5-a]pyrazin-8(7H)-one (80 mg, 0.230 mmol) and (S)-3-methylmorpholine (0.039 ml, 0.343 mmol) were mixed in NMP (2 mL) and DIPEA (148 mg, 0.2 ml, 1.1 mmol).
The reaction was heated for 6.5 hours at 250°C, in the microwave oven. The reaction was purified directly by preparative LC-MSto give (S)-7-(4-methoxybenzyl)-6-methyl-3-(3methylmorpholino)imidazo[1,5-a]pyrazin-8(7H)-one (10 mg, 0.028 mmol) in 12% yield.
H NMR (500 MHz, Chloroform-d) δ 8.00 (s, 1H), 7.18 (d, J = 7.1 Hz, 2H), 6.90 (d, J = 7.1 Hz,, 2H), 6.79 (s, 1H), 5.23 (d, J= 14.0 Hz, 1H), 5.13 (d, J = 15.7 Hz, 1H), 3.94 (m, 1H), 3.85 (m, 1 H), 3.81 (s. 3H), 3.60 (m, 1 H), 3.48 (dd, J = 11.7, 7.9 Hz, 1 H), 3.32 (t, J = 10.3 Hz, 1 H), 3.22 (d, J= 12.2 Hz, 1H), 2.28 (d, J = 1.6 Hz, 3H), 1.29 (td, J = 7.1, 1.6 Hz, 1H), 1.00 (dd, J = 6.4, 1.5 Hz, 3H).
141
LC-MS: iR = 0.65 min (method 7), mlz = 369.1 [M + H]+.
Example 97:
7-(4-methoxybenzyl)-6-methyi-3-(1,4-oxazepan-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one:
3-bromo-7-(4-methoxybenzyl)-6-methy!imidazo[1,5-a]pyrazin-8(7H)-one (149 mg, 0.428 mmol) and 1,4-oxazepane hydrochloride (100 mg, 0.727 mmol) were mixed in NMP (2.2 mL) and DIPEA (296 mg, 0.4 mL, 2.29 mmol). The reaction was heated for 3 hours at 250eC.
The reaction was purified directiy via préparative LC-MSto afford 7-(4-methoxybenzyl)-6methyl-3“(1,4-oxazepan-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one (27 mg, 0.073 mmol) in 17% yield.
Ή NMR (500 MHz, Chloroform-cQ δ 7.84 (s, 1H), 7.14 (m, 2H), 6.87 (m, 2H), 6.64 (s, 1H),
5.13 (s, 2H), 3.93 (m, 2H), 3.88 (m, 2H), 3.80 (d, J = 1.7 Hz, 3H), 3.73 (m, 4H), 2.22 (s, 3H), 2.09 (m, 2H).
LC-MS: tR = 0.56 min (method 7), mlz = 369.1 [M + H]*.
Example 98:
O
3-(2,2-dimethylmorpholino)-7-(4-methoxybenzyl)-6-methylimidazo[1,5-a]pyrazin-8(7H)one:
142
To a mixture of 3-bromo-7-(4-methoxybenzyl)-6-methylimidazo[1,5-a]pyrazin-8(7H)-one (500 mg, 1.44 mmol) and 2,2-dimethylmorpholine (331 mg, 2.88 mmol) in DMSO (5 mL) were added CsF (328 mg, 2.88 mmol) and K2CO3(299 mg, 2.88 mmol). The mixture was stirred at 100°C for 24 hours. The mixture was diluted with water (20 mL) and extracted with DCM (10 mL x 3). The combined organic layer was washed with water (10 mL χ 2); dried over Na2SO4 and evaporated under vacuum. The residue was purified by preparative TLC (ethyl acetate) to give 3-(2,2-dimethylmorpholino)-7-(4-methoxybenzyl)-6-methylimidazo[1,5-a]pyrazin8(7H)-one (15 mg, 3% yield).
’H NMR (CDCI3 400 MHz): δ 7.75 (s, 1 H), 7.15 (d, J = 8.8 Hz, 2H), 6.85 (d, J = 8.8 Hz. 2H),
6.60 (s, 1H), 5.15 (s, 2H), 3.93 (t, J = 4.8 Hz, 2H), 3.79 (s, 3H), 3.16 (t, J = 4.8 Hz, 2H), 2.98 (s, 2H), 2.18 (s, 3H), 1.37 (s, 6H).
LC-MS: (R = 2.26 min (method 13), m/z = 383.1 [M + H] *.
Example 99:
7-(3-fluorobenzyl)-3-(hexahydro-4H-furo[3,2-b]pyrrol-4-yl)-6-methylimidazo[1,5a]pyrazin-8(7H)-one, stereoisomer 1 and 2:
Step 1: To a solution of 3-bromo-6-methylimidazo[1,5-a]pyrazin-8(7/7)-one (3 g, 13.16 mmol) and 1-(bromomethyl)-3-fluorobenzene (2.99 g, 15.79 mmol) in DMF (50 mL) was added K2CO3 (3.64 g, 26.3 mmol). The mixture was stirred at 60°C for 12 hours. The mixture was diluted with water (100 mL) and extracted with EtOAc (50 mL χ 3). The combined organic layer was washed with water (50 mL χ 2); dried over Na2SO4 and evaporated under vacuum. The residue was washed with EtOAc (10 mL) and filtrated. The filter cake was dried under vacuum to give 3-bromo-7-(3-fluorobenzyl)-6-methylimidazo[1,5-a]pyrazîn-8(7/7)-one (2 g, 45% yield).
Step 2:To a mixture of 3-bromo-7-(3-fluorobenzyl)-6-methylimidazo[1,5-a]pyrazin-8(7/-/)-one (1.2 g, 3.57 mmol) and hexahydro-2/7-furo[3,2-b]pyrrole (0.5 oxalc acid sait) (678 mg, 4.28 mmol) in DMSO (20 mL) were added CsF (542 mg, 3.57 mmol) and K2CO3(1.23 g, 8.92
143 mmol). The mixture was stirred at 120°C for 72 hours. The mixture was diluted with water (100 mL) and extracted with DCM (50 mL * 3). The combined organic layer was washed with water (50 mL * 2); dried over Na2SO4and evaporated under vacuum. The residue was purified by prep- HPLC to give compound 3 (200 mg, 15% yield).
Step 3: 7-(3-fluorobenzyl)-3-(hexahydro-4H-furo[3,2-b]pyrrol-4-yl)-6-methylimidazo[1,5a]pyrazin-8(7/-/)-one (200 mg, 0.54 mmol) was purified by SFC to give stereoisomer 1 (48 mg).
Ή NMR (CDCh, 400 MHz): 5 7.74 (s, 1 H), 7.33 - 7.29 (m, 1 H), 7.01 - 6.89 (m, 3H), 6.73 (s, 1H), 5.19 (s, 2H), 4.72 - 4.66 (m, 2H), 3.92 - 3.86 (m, 2H), 3.75 - 3.73 (m, 1H), 3.50 - 3.47 (m, 1H), 2.16-2.09 (m, 6H), 1.91 - 1.86 (m, 1H).
LC-MS: tR = 1.90 min (method 12), m/z - 369.1 [M + H]+. SFC-MS: tR = 4.44 min, ee% > 99%. [α]ο20 +133.00 (c = 0.10, DCM).
stereoisomer 2 (32 mg).
'H NMR (CDCÎ3, 400 MHz): 5 7.74 (s, 1 H), 7.32 - 7.28 (m, 1 H), 7.01 - 6.89 (m, 3H), 6.73 (s, 1H), 5.19 (s, 2H), 4.74-4.67 (m, 2H), 3.92 - 3.87 (m, 2H), 3.75 - 3.72 (m, 1H), 3.50 - 3.47 (m, 1H), 2.16-2.09 (m. 6H), 1.91 - 1.86 (m, 1H).
LC-MS: tR = 1.89 min (method 12), m/z = 369.1 [M + H]+. SFC-MS: tR = 5.71 min, ee% > 99%. [ctjo 20 -82.00 (C = 0.10, DCM).
Example 100:
o
N
7-(3-fïuoΓobenzyl)-6-methyl·3-(tetrahydro-2W-pyΓan-3-yl)imidazo[1,5-alpyrazin-8(7H)one, stereoisomer 1 and 2:
Step 1 : To a solution of (3-methoxy-5-methylpyrazin-2-yl)methanamine (150 mg, 979.2 y mol), tetrahydro-2H-pyran-3-carboxylic acid (127.4 mg, 979.2 pmol) in DCM (10 mL) was added HATU (670.2 mg, 1.8 mmol) and triethylamine (198.2 mg, 1.9 mmol). The mixture was stirred at 25°C for 16 hours. The mixture was diluted with water (15 mL), extracted with
144
DCM (3 χ 30 mL). The combined organic layer was washed with brine (30 mL), dried over Na2SO4, filtered and concentrated. The residue was purified by preparative TLC (EA/MeOH=20/1) to give A/-((3-methoxy-5-methylpyrazin-2-yl)methyl)tetrahydro-2H-pyran-3carboxamide (130 mg, 50% yield).
Step 2: To a solution of A/-((3-methoxy-5-methylpyrazin-2-yl)methyl)tetrahydro-2/-/-pyran-3carboxamide (130 mg, 490 pmol) in dioxane (3 mL) was added POCI3 (1.28 g, 490 pmol). The mixture was stirred at 80°C for 3h. The mixture was cooled down to 25°C and concentrated. The residue was neutralized by saturated aq.NaHCO3, extracted with ethyl acetate (2 χ 20 mL). The combined organic layer was washed with brine (20 mL), dried over Na2SO4, filtered and concentrated to give crude 8-methoxy-6-methyl-3-(tetrahydro-2/-/-pyran3-yl)imidazo[1,5-a]pyrazine (120 mg, 99% yield). The crude was used directly for the next step.
Step 3: To a solution of 8-methoxy-6-methyl-3-(tetrahydro-2/-/-pyran-3-yl)imidazo[1,5a]pyrazine (120 mg, 485.3 pmol) in dioxane (3 mL) was added HCl (2 M, 3 mL). The mixture was stirred at 80°C for 3h. The mixture was cooled down to 25’C and concentrated, neutralized with saturated aq.NaHCO3, extracted with DCM (3 χ 30 mL). The combined organic layer was washed with brine (20 mL), dried over Na2SO4, filtered and concentrated to give crude 6-methyl-3-(tetrahydro-2H-pyran-3-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one (110 mg, 97% yield). The crude product was used directly for the next step.
Step 4: To a solution of 6-methyl-3-(tetrahydro-2/-/-pyran-3-yl)imidazo[1,5-a]pyrazin-8(7/-/)one (100.0 mg, 428.7 pmol) and 1-(bromomethyl)-3-fluorobenzene (121.6 mg, 643.0 pmol) in DMF (5 mL) was added K2CO3 (118.5 mg, 857.4 pmol). The mixture was stirred at 80°C for 2h. The mixture was cooled down to 25°C and diluted with water (20 mL), extracted with ethyl acetate (3 χ 30 mL). The combined organic layer was washed with brine (30 mL), dried over Na2SO4, filtered and concentrated. The residue was purified by preparative TLC (PE/EA=1/1) to give 7-(3-fluorobenzyl)-6-methyl-3-(tetrahydro-2H-pyran-3-yl)imidazo[1,5a]pyrazin-8(7/-/)-one (80 mg, 54% yield).
7-(3-fluorobenzyl)-6-methyl-3-(tetrahydro-2H-pyran-3-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one (80 mg, 234.3 pmol) was purified by SFC.
7-(3-fluorobenzyl)-6-methyl-3-(tetrahydro-2/-/-pyran-3-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one, stereisomer 1 (26 mg, 33% yield) was obtained.
145 ’H NMR(CDCI3400 MHz): 5 7.92 (s, 1H), 7.33-7.27 (m, 1H), 7.00-6.89 (m, 3H), 6.81 (s, 1 H), 5.23 (s, 2H), 4.11-4.03 (m, 2H), 3.69 (t, J = 11.2 Hz, 1H), 3.57-3.53 (m, 1H), 3.17-3.14 (m, 1H), 2.18-2.11 (m, 5H),1.85-1.79 (m, 2H).
LC-MS: fR = 2.06 min (method 3), m/z = 342.1 [M + H]*. SFC: tR = 5.286 min, ee% > 99%. a o20 = -3.0 (c = 0.10, CHCI3).
7-(3-fluorobenzyl)-6-methyl-3-(tetrahydro-2H-pyran-3-y!)imidazo[1,5-a]pyrazin-8(7/-/)-one, stereoisomer 2 (28 mg, yield: 35%) was obtained.
’H NMR (CDCI3 400 MHz): 5 7.92 (s, 1H), 7.31-7.27 (m, 1H), 7.00-6.89 (m, 3H), 6.81 (s, 1H), 5.22 (s, 2H), 4.11-4.03 (m, 2H), 3.68 (t, J = 11.2 Hz, 1H), 3.57-3.53 (m, 1H), 3.17-3.14 (m, 1H), 2.18-2.11 (m, 5H), 1.84-1.78 (m, 2H).
LC-MS: tR = 2.06 min (method 3), m/z = 342.2 [M + H]+. SFC: tR = 6.404 min, ee% > 99%. σ Dï0 =+3.0(c = 0.10, CHCI3).
IN VITRO TESTING
PDE1 INHIBITION ASSAY
PDE1A, PDE1B and PDE1C assays were performed as follows: the assays was performed in 60 pL samples containing a fixed amount of the PDE1 enzyml (sufficient to convert 2025% of the cyclic nucléotide substrate), a buffer (50 mM HEPES pH 7.6; 10 mM MgCI2; 0.02% Tween20), 0.1 mg/ml BSA, 15 nM tritium labelled cAMP and varying amounts of inhibitors. Reactions were initiated by addition of the cyclic nucléotide substrate, and reactions were allowed to proceed for 1 h at room température before being terminated through mixing with 20 pL (0.2 mg) yttrium silicate SPA beads (PerkinElmer). The beads were allowed to settle for 1 h in the dark before the plates were counted in a Wallac 1450 Microbeta counter. The measured signais were converted to activity relative to an uninhibited control (100%) and ICS0 values were calculated using XIFit (model 205, iDBS).
PDE9 INHIBITION ASSAY
A PDE9 assay may for example, be performed as follows: The assay is performed in 60 pL samples containing a fixed amount of the relevant PDE enzyme (sufficient to convert 2025% of the cyclic nucléotide substrate), a buffer (50 mM HEPES7.6; 10mM MgCI2; 0.02%
Claims (10)
- Ciaims1. A compound according to formula (I)(I) wherein n is 0 or 1;q is 0 or 1;R1 is selected from the group consisting of benzyl, indanyl, indoline and 5-membered heteroaryls; ail of which can be substituted with a substituent selected from the group consisting of halogen and C^Cs alkyl; orR1 is selected from the group consisting of saturated monocyclic rings containing 4-6 carbon atoms and 1-2 nitrogen atoms; ail of which can be substituted one or more times with one or more substituents selected from the group consisting of methyl, fluorine and sulfonamide; orR1 is selected from the group consisting of lactams containing 4-6 carbon atoms; ail of which can be substituted one or more times with one or more substituents selected from the group consisting of methyl and fluorine; orR1 is selected from the group consisting of bicyclic ethers including 7oxabicyclo[2.2.1]heptane; ail of which can be substituted one or more times with one or more substituents selected from the group consisting of methyl and fluorine; orR1 is selected from the group consisting of linear or branched Ο,-Ca alkyl, saturated monocyclic C3-C8 cycloalkyl, oxetanyl, tetrahydrofuranyï and tetrathydropyranyï; ail of which can be substituted one or more times with one or more substituents selected from the group consisting of methyl, fluorine, hydroxy, cyano or methoxy; orR1 is a linear or branched CrC3 alkyl, which is substituted with a substituent selected from phenyl and 5-membered heteroaryl, wherein said 5-membered heteroaryl can be substituted with one or more C^-Cs alkyls; or148R1 is selected from the group consisting of morpholine, tetrahydrofuran-3-amine, hexahydro2/-/-furo[3,2-b]pyrrole and homomorpholine; ail of which can be subsituted with one or more substituents selected from the group consisting of Ci-C3 alkyl;R2 is selected from the group consisting of hydrogen, linear or branched C-|-C8 alkyl, phenyl, saturated monocyclic C3-C8 cycloalkyl, oxetanyl, benzo[d][1,3]dioxolyl, tetrahydrofuranyl and tetrahydropyranyï; orR2 is phenyl or pyridyl substituted with one or more substituents selected from the group consisting of hydroxyl, amino, cyano, halogen, C,-C3 alkyl, CrC3 alkoxy, C3-C5 cycioalkoxy, C3-C5 cycloalkyl-methoxy, C-i-C3 fluoroalkoxy, and -NC(O)CH3; orR2 is a 5-membered heteroaryl which can be substituted with one or more CfC3 alkyi;R3 is selected from the group consisting of halogen, C^-Cs alkyl, C3-C5 cycloalkyl and phenyl; orR3 is selected from the group consisting of phenyl substituted one or more times with CrC3 alkyl; methyl substituted one, two or three times with fluorine; ethyl substituted one, two or three times with fluorine;R4 is hydrogen;and tautomers and pharmaceutically acceptable addition salts thereof.
- 2. The compound according to claim 1, whereinR1 is selected from the group consisting of linear or branched Ci-Cs alkyl, saturated monocyclic C3-C8 cycloalkyl, oxetanyl, tetrahydrofuranyl, and tetrahydropyranyï;R2 is selected from the group consisting of, linear or branched CvCa alkyl, phenyl, and saturated monocyclic C3-C8 cycloalkyl; orR2 is selected from the group consisting of phenyl substituted with a substituent selected from the group consisting of halogen, alkyl and methoxy;R3 is selected from the group consisting of Ci-C3 alkyl and halogen;R4 is hydrogen.149
- 3. The compound of claim 1, wherein R1 is selected from tetrahydrofuranyl and tetrahydropyranyl.
- 4. The compound of claim 1, wherein the compound is selected from the group consisting of:6-Benzyl-7-(3-fluorobenzyl)-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one;6- Benzyl-7-(cyclohexylmethyl)-3-(tetrahydro-2H-pyran-4-yl)<midazo[1,5-a]pyrazin-8(7/-/)-one;7- (Cyclohexylmethyl)-6-methyl-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one;7-(3-Fluorobenzyl)-6-methyl-3-(tetrahydro-2/7-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one;7-(4-Chlorobenzyl)-6-methyl-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one;6- Bromo-7-(3-fluorobenzyl)-3-(tetrahydro-2/7-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one;7- Benzyl-6-methyl-3-(tetrahydro-2/7-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one;7-(2-Fluorobenzyl)-6-methyl-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one;7-(3-Chlorobenzyl)-6-methyl-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/7)-one;7-(2-Chlorobenzyl)-6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1l5-a]pyrazin-8(7/-/)-one;7-(3-Methoxybenzyl)-6-methyl-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one;6-Methyl-7-(2-methylbenzyl)-3-(tetrahydro-2H-pyran-4-yl)imidazo[1l5-a]pyrazin-8(7/-/)-one;6- Methyl-7-(4-methylbenzyl)-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)'One;7- (4-Methoxybenzyl)-6-methyl-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one;7-(4-Fluorobenzyl)-6-methyl-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/7)-one;6- Methyl-7-(3-methylbenzyl)-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one;7- (3-fluorobenzyl)-6-methyl-3-(4-methyltetrahydro-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin8(7H)-one;4-(7-(3-fluorobenzyl)-6-methyl-8-oxo-7,8-dihydroimidazo[1,5-a]pyrazin-3-yl)tetrahydro-2/-/pyran-4-carbonitrile;1507-(3-fluorobenzyl)-3-(4-methoxytetrahydro-2H-pyran-4-yl)-6-methylimidazo[1l5-a]pyrazin8(7H)-one;7-(3-fluorobenzyl)-3-(4-fluorotetrahydro-2/7-pyran-4-yl)-6-methylimidazo[1,5-a]pyrazin-8(7/-/)one;(R) -7-(3-fluorobenzyl)-6-methyl-3-(tetrahydro-2/4-pyran-2-yl)imidazo[1l5-a]pyrazin-8(7H)one, (S) -7-(3-fluorobenzyl)-6-methyl-3-(tetrahydro-2/7-pyran-2-yl)imidazo[1,5-a]pyrazin-8(7/7)one;(R) -7-(3-fluorobenzyl)-6-methyl-3-(tetrahydrofuran-3-yl)imidazo[1,5-a]pyrazin-8(7H)-one;(S) -7-(3-fluorobenzyl)-6-methyl-3-(tetrahydrofuran-3-yl)imidazo[1,5-a]pyrazîn-8(7H)-one;(R) -7-(3-fluorobenzyl)-6-methyl-3-(3-methyltetrahydrofuran-3-yl)imidazo[1,5-a]pyrazin-8(7/-/)one;(S) -7-(3-fluorobenzyl)-6-methyl-3-(3-methyltetrahydrofuran-3-yl)imidazo[1,5-a]pyrazin-8(7/-/)one;7-(3-fluorobenzyl)-6-methyl-3-(1-nriethylcyciopropyl)imidazo[1,5-a]pyrazin-8(7/-/)-one ;3-(2,2-difluorocyclopropyl)-7-(3-fluorobenzyl)-6-methylimidazo[1,5-a]pyrazin-8(7/-/)-one;7-(3-fluorobenzyl)’6-methyl-3-((1R,2S)-2-methylcyclopropyl)imidazo[1,5-a]pyrazin-8(7/-/)one,7-(3-fluoiObenzyl)-6-methyl-3-((1R,2R)-2-methylcyclopropyl)imidazo[1,5-a]pyrazin-8(7H)one;7-(3-fluorobenzyl)-6-methyl-3-((1S,2S)-2-methylcyclopropyl)imidazo[1,5-a]pyrazin-8(7/7)one;7-(3-fluorobenzyl)-6-methyl-3-((1S[2R)-2-methylcyclopropyl)imidazo[1,5-a]pyrazin-8(7H)one;7-(3-fluorobenzyl)-6-methyl-3-((2S,3R)-2-methyltetrahydrofuran-3-yl)imidazo[1,5-a]pyrazin8(7H)-one;7-(3-fluorobenzyl)-6-methyl-3-((2S,3S)-2-methyltetrahydrofuran-3-yl)imidazo[1,5-a]pyrazin8(7H)-one;1517-(3-fluorobenzyl)-6-methyl-3-((2R3R)-2-methyltetrahydrofuran-3-yl)imidazo[1,5-a]pyrazin8(7H)-one;7-(3-fluorobenzyl)-6-methyl-3-((2R,3S)-2-methyltetrahydrofuran-3-yl)imidazo[1,5-a]pyrazin8(7/-/)-one;7-(3-fluorobenzyl)-3-((1R,2S)-2-fluorocyclopropyl)-6-methylimidazo[1,5-a]pyrazin-8(7H)-one;7-(3-fluorobenzyl)-3-((1R,2R)-2-fluorocyclopropyl)-6-methylimidazo[1,5-a]pyrazin-8(7/-/)-one;7-(3-fluorobenzyl)-3-((1S,2S)-2-fluorocyclopropyl)-6-methylimidazo[1,5-a]pyrazin-8(7/-/)-one;7-{3-fluorobenzyl)-3-((1S,2R)-2-fluorocyclopropyl)-6-methylimidazo[1,5-a]pyrazin-8(7/-/)-one;7-(4-cyclopropoxybenzyl)-6-methyl-3’(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)one;7-(4-(difluoromethoxy)benzyl)-6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin8(7H)-one;6- methyl-3-(tetrahydro-2/-/-pyran-4-yl)-7-(4-(trifluoromethoxy)benzyl)imidazo[1,5-a]pyrazin-8(7H)-one;7- (4-(cyclopropylmethoxy)benzyl)-6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5a]pyrazin-8(7H)-one;7-benzyl-6-ethyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one;6- ethyl-7-(4-methoxybenzyl)-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one;3- ((6-methyl-8-oxo-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1r5-a]pyrazin-7(8H)yi)methyl)benzonitrîle;4- ((6-ΓΠθίΗγΙ-8-οχο-3-(1θίΓ3Μγ0Γο-2/-/-ργΓ3η-4-γΙ)ίπΊίά3Ζθ[115-3]ργΓ3ΖΪη-7(8Η)yl)methyl)benzonitrile;A/-(4-((6-methyl-8-oxo-3-(tetrahydro-2/-/-pyran-4-y!)imidazo[1,5-a]pyrazin-7(8H)yl)methyl)phenyl)acetamide;7- (4-chloro-3-methoxybenzyl)-6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin’8(7H)-one;7-(2-ethylbenzyl)-6-methyl-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one;1527-(benzo[d][1,3]dtoxol-5-ylmethyl)-6-methyl-3-(tetrahydro-2/7-pyran-4-yl)irnidazo[1,5a]pyrazin-8(7/-/)-one;7-(3-chloro-4-methoxybenzyl)-6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin8(7H)-one;7-(4-aminobenzyl)-6-methyl-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one;7-(4-hydroxybenzyl)-6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[115-a]pyrazin-8(7/-/)-one;6- ethyl-7-(3-fluorobenzyl)-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one;7- (4-methoxybenzyl)-6-methyl-3-((2SÉ3R)-2-methyltetrahydrofuran-3-yl)imidazo[1,5a]pyrazin-8(7H)-one;7-(4-methoxybenzyl)-6-methyl-3-((2St3S)-2-methyltetrahydrofuran-3-yl)imidazo[1,5a]pyrazin-8(7H)-one;7-(4-methoxybenzy!)-6-methyl-3-((2R,3R)-2-methyitetrahydrofuran-3-yl)imidazo[1,5a]pyrazin-8(7H)-one;7-(4-methoxybenzyl)-6-methyl-3-((2R,3S)-2-methyltetrahydrofuran-3-yl)imidazo[1,5a]pyrazin-8(7H)-one;7-(4-methoxybenzyl)-6-rïiethyl-3-propylimidazo[1,5-a]pyrazin-8(7/-/)-one;7-((6-methoxypyridin-3-yl)methyl)-6-methyl-3-(tetrahydro-2/-/-pyran-4-yl)innidazo[1,5a]pyrazin-8(7H)-one;6,7-dimethyl-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one,7-ethyl-6-methyl-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[115-a]pyrazin-8(7/-/)-one;6- methyl-7-propyl-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one;7- isopropyl-6-methyl-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one;7-isopentyl-6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one;7-(cyclopentylmethyl)-6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-f)-one;2-((6-methyl-8-oxo-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-7(8H)yl)methyl)benzonitriie;7-(cycloheptylmethyl)-6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-orie;1537-(4-methoxybenzyl)-6-nnethyl-3-(3-methyltetrahydro-2/7-pyran-4-yl)imidazo[1,5-a]pyrazin8(7/-/)-one;7-(4-methoxybenzyl)-6-methyl-3-((1 R,2R,4S)-2-methyl-7-oxabicyclo[2.2.1]heptan-2y!)imidazo[1,5-a]pyrazin-8(7/-/)-one;(S)-7-(4-methoxybenzyl)-6-methyl-3-(1-phenylethyl)imidazo[1,5-a]pyrazin-8(7/-/)-one;(R)-7-(4-methoxybenzyl)-6-methyl-3-(1-phenylethyl)imidazo[1,5-a]pyrazin-8(7/7)-one;3-(1,4-dimethylpiperidin-4-yl)-7-(4-methoxybenzyl)-6-methylimidazo[1,5-a]pyrazin-8(7/7)-one;3-(6-chloro-2!3-dihydro-1/7-inden-1-y1)-7-(4-methoxybenzyl)-6-methylimidazo[1,5-a]pyrazin8(7H)-one;7-(4-methoxybenzyl)-6-methyl-3-(3-methyl-5-oxopyrrolidin-3-yl)imidazo[1,5-a]pyrazin-8(7/-/)one;3-(1-methoxy-2-methy!propan-2-yl)-7-(4-methoxybenzyl)-6-methylimidazo[1,5-a]pyrazin8(7H)-one;3-isopropy!-7-(4-methoxybenzy!)-6-methylimidazo[1,5-a]pyrazin-8(7H)-one;6-methyl-7-((2-methylthiazol-4-yl)methyl)-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin8(7/-/)-one;6-methyl-3-(tetrahydro-2/-/-pyran-4-yl)-7-(thiophen-3-ylmethyl)imidazo[1,5-a]pyrazin-8(7/-/)one;6- methyl-3-(tetrahydro-2/-/-pyran-4-yl)-7-(thiazol-4-ylmethyl)imidazo[1,5-a]pyrazin-8(7/-/)-one;7- ((3,5-dimethylisoxazol-4-yl)methyl)-6-methyl-3-(tetrahydro-2/7-pyran-4-yl)imidazo[1,5a]pyrazin-8(7/-/)-one;6-methyl-7-((5-methyIisoxazol-3-yl)methyl)-3-(tetrahydro-2/7-pyran-4-yl)îmidazo[1,5a]pyrazin-8(7H)-one;6- methyl-7-((3-methylisoxazol-5-yl)methyl)-3-(tetrahydro-2/7-pyran-4-yl)imidazo[1,5a]pyrazin-8(7/7)-one;3-(2,6-dimethyitetrahydro-2/-/-pyran-4-yl)-7-(4-methoxybenzyl)-6-methylimidazo[1,5a]pyrazin-8(7/-/)-one;7- (cyclohexylmethyl)-6-methyl-3-propylimidazo[1,5-a]pyrazin-8(7/-/)-one;1543-(2-hydroxypropan-2-yl)-7-(4-methoxybenzyl)-6-methylimidazo[1,5-a]pyrazin-8(7H)-one;3-(2-fluoropropan-2-yl)-7-(4-methoxybenzyl)-6-methylimidazo[1,5-a]pyrazin-8(7H)-one;7-(4-methoxybenzyl)-6-methyl-3-(7-oxoazepan-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one;7-(4-methoxybenzyl)-6-methyl-3-(5-methyltetrahydrofuran-3-yl)imidazo[1,5-a]pyrazin-8(7H)one;7-(4-methoxybenzyl)-6-methyl-3-(1-(4-methylthiazol-2-yl)ethyl)imidazo[1,5-a]pyrazin-8(7H)one;3-(7-(4-methoxybenzyl)-6-methyl-8-oxo-7,8-dihydroimidazo[1l5-a]pyrazin-3-yî)-3methylpyrrolidine-1-sulfonamide;6- (cyclopentylmethyl)-7-(4-methoxybenzyl)-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5a]pyrazin-8(7H)-one;3-(morpholino)-7-(4-methoxybenzyl)-6-methylimidazo[1,5-a]pyrazin-8(7/-/)-one;7- (4-methoxybenzyl)-6-methyl-3-((tetrahydrofuran-3-yl)amino)imidazo[1,5-a]pyrazin-8(7/-/)one;(R) ’7-(4-methoxybenzyl)-6-methyl-3-(3-methylmorpholino)imidazo[1,5-a]pyrazin-8(7H)-one;(S) -7-(4-methoxybenzyl)-6-methyl-3-(3-methylmorpholino)imidazo[1,5-a]pyrazin-8(7H)-one;7-(4-methoxybenzyl)-6-methyl-3-(1,4-oxazepan-4-yl)imidazo[1,5-a]pyrazin-8(7/7)“One;3-(2,2-dimethylmorpholino)-7-(4-methoxybenzyl)-6-methylimidazo[1,5-a]pyrazin-8(7/7)-one;7-(3-fluorobenzyl)-3-((3aS,6aS)-hexahydro-4/7-furo[3,2-b]pyrrol-4-yl)-6-methylimidazo[115a]pyrazin-8(7H)-one7-(3-fIuorobenzyl)-3-((3a/?l6aR)-hexahydro-4H-furo[3l2-b]pyrrol-4-yl)-6-methylimidazo[1,5a]pyrazin-8(7/-/)-one;(R) -7-(3-fluorobenzyl)-6-methyl-3-(tetrahydro-2H-pyran-3-yI)imidazo[1,5-a]pyrazin-8(7/-/)one;(S) -7-(3-fluorobenzyl)-6-methyl-3-(tetrahydro-2H-pyran-3-yl)imidazo[1,5-a]pyrazin-8(7H)one;or a pharmaceutically acceptable sait of any of these compounds.155
- 5. The compound according to claim 1 which is7-(Cyclohexylmethyl)-6-methyl-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7H)-one; or a pharmaceutically acceptable sait thereof.
- 6. The compound according to claim 1 which is6- Methyl-7-(4-methylbenzyl)-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one; or a pharmaceutically acceptable sait thereof.
- 7. The compound according to claim 1 which is7- (4-Methoxybenzyl)-6-methyl-3-(tetrahydro-2H-pyran-4-yl)imidazo[1,5-a]pyrazin-8(7/-/)-one; or a pharmaceutically acceptable sait thereof.
- 8. The compound according to claim 1 which is7-(benzo[d][1,3]dioxol-5-ylmethyl)-6-methyl-3-(tetrahydro-2/7-pyran-4-yl)imidazo[1(5a]pyrazin-8(7H)-one;or a pharmaceutically acceptable sait thereof.
- 9. The compound according to claim 1 which is7-((6-methoxypyridin-3-yl)methyl)-6-methyl-3-(tetrahydro-2/-/-pyran-4-yl)imidazo[1,5a]pyrazin-8(7H)-one;or a pharmaceutically acceptable sait thereof.
- 10. The compound according to claim 1 which is7-(cycloheptylmethyl)-6-methy!-3-(tetrahydro-2H-pyran-4-yl)imidazo[1l5-a]pyrazin-8(7/7)-one;
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