ES2270143T3 - Compuestos organicos como agentes para el tratamiento de condiciones mediadas por aldosterona. - Google Patents

Info

Publication number

ES2270143T3

ES2270143T3 ES03784194T ES03784194T ES2270143T3 ES 2270143 T3 ES2270143 T3 ES 2270143T3 ES 03784194 T ES03784194 T ES 03784194T ES 03784194 T ES03784194 T ES 03784194T ES 2270143 T3 ES2270143 T3 ES 2270143T3

Authority

ES

Spain

Prior art keywords

imidazo

pyrazin

phenyl

dihydro

bromo

Prior art date

2002-08-07

Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)

Expired - Lifetime

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• Espacenet
• Global Dossier
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• PQSUYGKTWSAVDQ-ZVIOFETBSA-N Aldosterone Chemical compound C([C@@]1([C@@H](C(=O)CO)CC[C@H]1[C@@H]1CC2)C=O)[C@H](O)[C@@H]1[C@]1(C)C2=CC(=O)CC1 PQSUYGKTWSAVDQ-ZVIOFETBSA-N 0.000 title description 8
• PQSUYGKTWSAVDQ-UHFFFAOYSA-N Aldosterone Natural products C1CC2C3CCC(C(=O)CO)C3(C=O)CC(O)C2C2(C)C1=CC(=O)CC2 PQSUYGKTWSAVDQ-UHFFFAOYSA-N 0.000 title description 8
• 229960002478 aldosterone Drugs 0.000 title description 8
• 230000001404 mediated effect Effects 0.000 title description 4
• 150000002894 organic compounds Chemical class 0.000 title description 2
• 150000001875 compounds Chemical class 0.000 claims abstract description 218
• 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 102
• 239000001257 hydrogen Substances 0.000 claims abstract description 97
• 125000000217 alkyl group Chemical group 0.000 claims abstract description 90
• -1 9H-carbazol-2-yl Chemical group 0.000 claims abstract description 80
• 239000000203 mixture Substances 0.000 claims abstract description 78
• 150000002431 hydrogen Chemical class 0.000 claims abstract description 72
• 230000003287 optical effect Effects 0.000 claims abstract description 50
• 125000003118 aryl group Chemical group 0.000 claims abstract description 47
• 229910052760 oxygen Inorganic materials 0.000 claims abstract description 45
• 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 32
• 125000001072 heteroaryl group Chemical group 0.000 claims abstract description 30
• 125000000623 heterocyclic group Chemical group 0.000 claims abstract description 29
• 125000003710 aryl alkyl group Chemical group 0.000 claims abstract description 28
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 27
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 22
• 125000004475 heteroaralkyl group Chemical group 0.000 claims abstract description 22
• 239000001301 oxygen Substances 0.000 claims abstract description 17
• QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 16
• IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 15
• 229910052736 halogen Inorganic materials 0.000 claims abstract description 14
• 150000002367 halogens Chemical class 0.000 claims abstract description 14
• 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims abstract description 12
• 125000000609 carbazolyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 claims abstract description 11
• 125000003342 alkenyl group Chemical group 0.000 claims abstract description 9
• 125000000304 alkynyl group Chemical group 0.000 claims abstract description 8
• 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 8
• 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims abstract description 6
• 125000000547 substituted alkyl group Chemical group 0.000 claims abstract description 6
• 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 claims abstract description 5
• 150000003839 salts Chemical class 0.000 claims description 58
• JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Substances N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 claims description 35
• 239000002253 acid Substances 0.000 claims description 25
• 125000003545 alkoxy group Chemical group 0.000 claims description 21
• 125000004414 alkyl thio group Chemical group 0.000 claims description 21
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 21
• 239000008194 pharmaceutical composition Substances 0.000 claims description 20
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 20
• 206010020772 Hypertension Diseases 0.000 claims description 19
• 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 19
• 239000003795 chemical substances by application Substances 0.000 claims description 18
• 108010009911 Cytochrome P-450 CYP11B2 Proteins 0.000 claims description 15
• 102100024329 Cytochrome P450 11B2, mitochondrial Human genes 0.000 claims description 15
• 125000004432 carbon atom Chemical group C* 0.000 claims description 15
• 125000001424 substituent group Chemical group 0.000 claims description 15
• 230000000694 effects Effects 0.000 claims description 14
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 14
• 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 14
• 125000003282 alkyl amino group Chemical group 0.000 claims description 13
• 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 13
• 125000004663 dialkyl amino group Chemical group 0.000 claims description 13
• 125000005420 sulfonamido group Chemical group S(=O)(=O)(N*)* 0.000 claims description 13
• 125000002252 acyl group Chemical group 0.000 claims description 12
• 125000003396 thiol group Chemical class [H]S* 0.000 claims description 12
• 125000004423 acyloxy group Chemical group 0.000 claims description 11
• 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims description 11
• 239000003814 drug Substances 0.000 claims description 11
• 238000002360 preparation method Methods 0.000 claims description 11
• 125000004442 acylamino group Chemical group 0.000 claims description 10
• 125000005110 aryl thio group Chemical group 0.000 claims description 9
• 125000004093 cyano group Chemical group *C#N 0.000 claims description 9
• 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 9
• 125000004104 aryloxy group Chemical group 0.000 claims description 8
• 125000001589 carboacyl group Chemical group 0.000 claims description 8
• 239000004041 inotropic agent Substances 0.000 claims description 8
• 125000002950 monocyclic group Chemical group 0.000 claims description 8
• 201000001320 Atherosclerosis Diseases 0.000 claims description 7
• 206010007559 Cardiac failure congestive Diseases 0.000 claims description 7
• 102000008186 Collagen Human genes 0.000 claims description 7
• 108010035532 Collagen Proteins 0.000 claims description 7
• 206010016654 Fibrosis Diseases 0.000 claims description 7
• 206010019280 Heart failures Diseases 0.000 claims description 7
• 208000019025 Hypokalemia Diseases 0.000 claims description 7
• 208000008589 Obesity Diseases 0.000 claims description 7
• 208000001647 Renal Insufficiency Diseases 0.000 claims description 7
• 230000015572 biosynthetic process Effects 0.000 claims description 7
• 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 7
• 229920001436 collagen Polymers 0.000 claims description 7
• 208000029078 coronary artery disease Diseases 0.000 claims description 7
• 230000004761 fibrosis Effects 0.000 claims description 7
• 125000002883 imidazolyl group Chemical group 0.000 claims description 7
• 201000006370 kidney failure Diseases 0.000 claims description 7
• 235000020824 obesity Nutrition 0.000 claims description 7
• 125000004043 oxo group Chemical group O=* 0.000 claims description 7
• 208000024896 potassium deficiency disease Diseases 0.000 claims description 7
• 238000007634 remodeling Methods 0.000 claims description 7
• 208000037803 restenosis Diseases 0.000 claims description 7
• 208000011580 syndromic disease Diseases 0.000 claims description 7
• 239000000883 anti-obesity agent Substances 0.000 claims description 6
• 229940125710 antiobesity agent Drugs 0.000 claims description 6
• 125000002619 bicyclic group Chemical group 0.000 claims description 6
• OQEIHCXNKZOMQH-UHFFFAOYSA-N 4-(8-benzyl-7-oxo-6,9-dihydro-5h-imidazo[1,5-a][1,4]diazepin-5-yl)benzonitrile Chemical compound N12C=NC=C2CN(CC=2C=CC=CC=2)C(=O)CC1C1=CC=C(C#N)C=C1 OQEIHCXNKZOMQH-UHFFFAOYSA-N 0.000 claims description 5
• KGROSPWRIWFUBR-UHFFFAOYSA-N 4-[7-(cyclopropylmethyl)-6-oxo-5,8-dihydroimidazo[1,5-a]pyrazin-5-yl]benzonitrile Chemical compound N12C=NC=C2CN(CC2CC2)C(=O)C1C1=CC=C(C#N)C=C1 KGROSPWRIWFUBR-UHFFFAOYSA-N 0.000 claims description 5
• JNSHAFSIADREGA-UHFFFAOYSA-N 5-(4-bromophenyl)-7-[(4-methoxyphenyl)methyl]-5,8-dihydroimidazo[1,5-a]pyrazin-6-one Chemical compound C1=CC(OC)=CC=C1CN1C(=O)C(C=2C=CC(Br)=CC=2)N2C=NC=C2C1 JNSHAFSIADREGA-UHFFFAOYSA-N 0.000 claims description 5
• BDWRUIAZTZPLSN-UHFFFAOYSA-N 7-[(4-methoxyphenyl)methyl]-5-(4-thiophen-3-ylphenyl)-5,8-dihydroimidazo[1,5-a]pyrazin-6-one Chemical compound C1=CC(OC)=CC=C1CN1C(=O)C(C=2C=CC(=CC=2)C2=CSC=C2)N2C=NC=C2C1 BDWRUIAZTZPLSN-UHFFFAOYSA-N 0.000 claims description 5
• 125000005161 aryl oxy carbonyl group Chemical group 0.000 claims description 5
• 125000002541 furyl group Chemical group 0.000 claims description 5
• 230000000055 hyoplipidemic effect Effects 0.000 claims description 5
• 208000010125 myocardial infarction Diseases 0.000 claims description 5
• 125000004076 pyridyl group Chemical group 0.000 claims description 5
• 125000000335 thiazolyl group Chemical group 0.000 claims description 5
• 125000001544 thienyl group Chemical group 0.000 claims description 5
• WXWMJWIKOZGKGJ-UHFFFAOYSA-N 3-(7-benzyl-6-oxo-5,8-dihydroimidazo[1,5-a]pyrazin-5-yl)benzonitrile Chemical compound N12C=NC=C2CN(CC=2C=CC=CC=2)C(=O)C1C1=CC=CC(C#N)=C1 WXWMJWIKOZGKGJ-UHFFFAOYSA-N 0.000 claims description 4
• 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims description 4
• MHFSWEVJOIPGPC-UHFFFAOYSA-N 7-benzyl-5-(4-bromophenyl)-5,8-dihydroimidazo[1,5-a]pyrazin-6-one Chemical compound C1=CC(Br)=CC=C1C1N2C=NC=C2CN(CC=2C=CC=CC=2)C1=O MHFSWEVJOIPGPC-UHFFFAOYSA-N 0.000 claims description 4
• 125000005333 aroyloxy group Chemical group 0.000 claims description 4
• 125000004470 heterocyclooxy group Chemical group 0.000 claims description 4
• 125000001041 indolyl group Chemical group 0.000 claims description 4
• 125000002757 morpholinyl group Chemical group 0.000 claims description 4
• 125000000714 pyrimidinyl group Chemical group 0.000 claims description 4
• BQZVGLJZGCOXHP-UHFFFAOYSA-N 4-(6-oxo-7-propan-2-yl-5,8-dihydroimidazo[1,5-a]pyrazin-5-yl)benzonitrile Chemical compound O=C1N(C(C)C)CC2=CN=CN2C1C1=CC=C(C#N)C=C1 BQZVGLJZGCOXHP-UHFFFAOYSA-N 0.000 claims description 3
• OLCNWVADTAJHOT-UHFFFAOYSA-N 4-(6-oxo-7-propyl-5,8-dihydroimidazo[1,5-a]pyrazin-5-yl)benzonitrile Chemical compound O=C1N(CCC)CC2=CN=CN2C1C1=CC=C(C#N)C=C1 OLCNWVADTAJHOT-UHFFFAOYSA-N 0.000 claims description 3
• ULAXZIVKDTZOBZ-UHFFFAOYSA-N 4-(7-benzyl-5-methyl-6-oxo-8h-imidazo[1,5-a]pyrazin-5-yl)benzonitrile Chemical compound C1C2=CN=CN2C(C)(C=2C=CC(=CC=2)C#N)C(=O)N1CC1=CC=CC=C1 ULAXZIVKDTZOBZ-UHFFFAOYSA-N 0.000 claims description 3
• PKHXGYUUXXTTBL-UHFFFAOYSA-N 4-(7-benzyl-6-oxo-5,8-dihydroimidazo[1,5-a]pyrazin-5-yl)benzonitrile Chemical compound N12C=NC=C2CN(CC=2C=CC=CC=2)C(=O)C1C1=CC=C(C#N)C=C1 PKHXGYUUXXTTBL-UHFFFAOYSA-N 0.000 claims description 3
• LFZXYWKNICMEKP-UHFFFAOYSA-N 4-(7-methyl-6-oxo-5,8-dihydroimidazo[1,5-a]pyrazin-5-yl)benzonitrile Chemical compound O=C1N(C)CC2=CN=CN2C1C1=CC=C(C#N)C=C1 LFZXYWKNICMEKP-UHFFFAOYSA-N 0.000 claims description 3
• CHMZUIQHLSUIFP-UHFFFAOYSA-N 4-[5-benzyl-7-(cyclopropylmethyl)-6-oxo-8h-imidazo[1,5-a]pyrazin-5-yl]benzonitrile Chemical compound C1C2=CN=CN2C(C=2C=CC(=CC=2)C#N)(CC=2C=CC=CC=2)C(=O)N1CC1CC1 CHMZUIQHLSUIFP-UHFFFAOYSA-N 0.000 claims description 3
• ANCYWORHVHQAIZ-UHFFFAOYSA-N 4-[7-[(4-fluorophenyl)methyl]-5-methyl-6-oxo-8h-imidazo[1,5-a]pyrazin-5-yl]benzonitrile Chemical compound C1C2=CN=CN2C(C)(C=2C=CC(=CC=2)C#N)C(=O)N1CC1=CC=C(F)C=C1 ANCYWORHVHQAIZ-UHFFFAOYSA-N 0.000 claims description 3
• REWJFOIXMYASRH-UHFFFAOYSA-N 4-[8-(cyclopropylmethyl)-7-oxo-6,9-dihydro-5h-imidazo[1,5-a][1,4]diazepin-5-yl]benzonitrile Chemical compound N12C=NC=C2CN(CC2CC2)C(=O)CC1C1=CC=C(C#N)C=C1 REWJFOIXMYASRH-UHFFFAOYSA-N 0.000 claims description 3
• IFDMLYRAZYXDPL-UHFFFAOYSA-N 5-(3-bromophenyl)-7-(cyclohexylmethyl)-5,8-dihydroimidazo[1,5-a]pyrazin-6-one Chemical compound BrC1=CC=CC(C2N3C=NC=C3CN(CC3CCCCC3)C2=O)=C1 IFDMLYRAZYXDPL-UHFFFAOYSA-N 0.000 claims description 3
• VLUHNNONLXRLDP-UHFFFAOYSA-N 5-(3-bromophenyl)-7-(furan-3-ylmethyl)-5,8-dihydroimidazo[1,5-a]pyrazin-6-one Chemical compound BrC1=CC=CC(C2N3C=NC=C3CN(CC3=COC=C3)C2=O)=C1 VLUHNNONLXRLDP-UHFFFAOYSA-N 0.000 claims description 3
• ZVDLMGVYQXTJGB-UHFFFAOYSA-N 5-(3-bromophenyl)-7-(pyridin-2-ylmethyl)-5,8-dihydroimidazo[1,5-a]pyrazin-6-one Chemical compound BrC1=CC=CC(C2N3C=NC=C3CN(CC=3N=CC=CC=3)C2=O)=C1 ZVDLMGVYQXTJGB-UHFFFAOYSA-N 0.000 claims description 3
• WDQGXPYKAOIHAH-UHFFFAOYSA-N 5-(3-bromophenyl)-7-(pyridin-3-ylmethyl)-5,8-dihydroimidazo[1,5-a]pyrazin-6-one Chemical compound BrC1=CC=CC(C2N3C=NC=C3CN(CC=3C=NC=CC=3)C2=O)=C1 WDQGXPYKAOIHAH-UHFFFAOYSA-N 0.000 claims description 3
• DUZSCKPDZXTNHU-UHFFFAOYSA-N 5-(3-bromophenyl)-7-(pyridin-4-ylmethyl)-5,8-dihydroimidazo[1,5-a]pyrazin-6-one Chemical compound BrC1=CC=CC(C2N3C=NC=C3CN(CC=3C=CN=CC=3)C2=O)=C1 DUZSCKPDZXTNHU-UHFFFAOYSA-N 0.000 claims description 3
• CXJIKIOJRDNKRH-UHFFFAOYSA-N 5-(3-bromophenyl)-7-(thiophen-3-ylmethyl)-5,8-dihydroimidazo[1,5-a]pyrazin-6-one Chemical compound BrC1=CC=CC(C2N3C=NC=C3CN(CC3=CSC=C3)C2=O)=C1 CXJIKIOJRDNKRH-UHFFFAOYSA-N 0.000 claims description 3
• JPRUCAHFHQKXSJ-UHFFFAOYSA-N 5-(4-bromophenyl)-7-methyl-5,8-dihydroimidazo[1,5-a]pyrazin-6-one Chemical compound O=C1N(C)CC2=CN=CN2C1C1=CC=C(Br)C=C1 JPRUCAHFHQKXSJ-UHFFFAOYSA-N 0.000 claims description 3
• MGGVICIZANYYQK-UHFFFAOYSA-N 5-[4-(4-chlorophenyl)phenyl]-7-[(4-methoxyphenyl)methyl]-5,8-dihydroimidazo[1,5-a]pyrazin-6-one Chemical compound C1=CC(OC)=CC=C1CN1C(=O)C(C=2C=CC(=CC=2)C=2C=CC(Cl)=CC=2)N2C=NC=C2C1 MGGVICIZANYYQK-UHFFFAOYSA-N 0.000 claims description 3
• YTJRDFYHQUXXCN-UHFFFAOYSA-N 5-benzyl-5-(4-bromophenyl)-7-[(4-fluorophenyl)methyl]-8h-imidazo[1,5-a]pyrazin-6-one Chemical compound C1=CC(F)=CC=C1CN1C(=O)C(CC=2C=CC=CC=2)(C=2C=CC(Br)=CC=2)N2C=NC=C2C1 YTJRDFYHQUXXCN-UHFFFAOYSA-N 0.000 claims description 3
• MVDJFHIGCJKAKH-UHFFFAOYSA-N 7-[(4-fluorophenyl)methyl]-5,8-dihydroimidazo[1,5-a]pyrazin-6-one Chemical compound C1=CC(F)=CC=C1CN1C(=O)CN2C=NC=C2C1 MVDJFHIGCJKAKH-UHFFFAOYSA-N 0.000 claims description 3
• UCDBANUXQWESGO-UHFFFAOYSA-N 7-[(4-fluorophenyl)methyl]-5-(4-phenylphenyl)-5,8-dihydroimidazo[1,5-a]pyrazin-6-one Chemical compound C1=CC(F)=CC=C1CN1C(=O)C(C=2C=CC(=CC=2)C=2C=CC=CC=2)N2C=NC=C2C1 UCDBANUXQWESGO-UHFFFAOYSA-N 0.000 claims description 3
• GHBPBVBYHXDIFZ-UHFFFAOYSA-N 7-[(4-methylphenyl)methyl]-5,8-dihydroimidazo[1,5-a]pyrazin-6-one Chemical compound C1=CC(C)=CC=C1CN1C(=O)CN2C=NC=C2C1 GHBPBVBYHXDIFZ-UHFFFAOYSA-N 0.000 claims description 3
• DBNHJIYTPWCCOH-UHFFFAOYSA-N 7-benzyl-5-(3-bromophenyl)-5,8-dihydroimidazo[1,5-a]pyrazin-6-one Chemical compound BrC1=CC=CC(C2N3C=NC=C3CN(CC=3C=CC=CC=3)C2=O)=C1 DBNHJIYTPWCCOH-UHFFFAOYSA-N 0.000 claims description 3
• LHQHSTYXNKDXTC-UHFFFAOYSA-N 7-benzyl-5-(3-phenylphenyl)-5,8-dihydroimidazo[1,5-a]pyrazin-6-one Chemical compound N12C=NC=C2CN(CC=2C=CC=CC=2)C(=O)C1C(C=1)=CC=CC=1C1=CC=CC=C1 LHQHSTYXNKDXTC-UHFFFAOYSA-N 0.000 claims description 3
• 229940079593 drug Drugs 0.000 claims description 3
• 230000007360 epithelial dysfunction Effects 0.000 claims description 3
• 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 3
• 125000002795 guanidino group Chemical group C(N)(=N)N* 0.000 claims description 3
• 125000005226 heteroaryloxycarbonyl group Chemical group 0.000 claims description 3
• 210000004165 myocardium Anatomy 0.000 claims description 3
• SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 claims description 3
• 201000001119 neuropathy Diseases 0.000 claims description 3
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• 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 claims description 3
• IUIFCWCDEZGVLL-AUUYWEPGSA-N (5r)-5-(3-bromophenyl)-7-[(1r)-1-phenylethyl]-5,8-dihydroimidazo[1,5-a]pyrazin-6-one Chemical compound C1([C@H]2N3C=NC=C3CN(C2=O)[C@H](C)C=2C=CC=CC=2)=CC=CC(Br)=C1 IUIFCWCDEZGVLL-AUUYWEPGSA-N 0.000 claims description 2
• IUIFCWCDEZGVLL-IFXJQAMLSA-N (5r)-5-(3-bromophenyl)-7-[(1s)-1-phenylethyl]-5,8-dihydroimidazo[1,5-a]pyrazin-6-one Chemical compound C1([C@H]2N3C=NC=C3CN(C2=O)[C@@H](C)C=2C=CC=CC=2)=CC=CC(Br)=C1 IUIFCWCDEZGVLL-IFXJQAMLSA-N 0.000 claims description 2
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• BNPIELKFNYKKES-IFXJQAMLSA-N (5r)-5-(4-bromophenyl)-7-[(1s)-1-phenylethyl]-5,8-dihydroimidazo[1,5-a]pyrazin-6-one Chemical compound C1([C@H]2N3C=NC=C3CN(C2=O)[C@@H](C)C=2C=CC=CC=2)=CC=C(Br)C=C1 BNPIELKFNYKKES-IFXJQAMLSA-N 0.000 claims description 2
• IUIFCWCDEZGVLL-KUHUBIRLSA-N (5s)-5-(3-bromophenyl)-7-[(1r)-1-phenylethyl]-5,8-dihydroimidazo[1,5-a]pyrazin-6-one Chemical compound C1([C@@H]2N3C=NC=C3CN(C2=O)[C@H](C)C=2C=CC=CC=2)=CC=CC(Br)=C1 IUIFCWCDEZGVLL-KUHUBIRLSA-N 0.000 claims description 2
• IUIFCWCDEZGVLL-LIRRHRJNSA-N (5s)-5-(3-bromophenyl)-7-[(1s)-1-phenylethyl]-5,8-dihydroimidazo[1,5-a]pyrazin-6-one Chemical compound C1([C@@H]2N3C=NC=C3CN(C2=O)[C@@H](C)C=2C=CC=CC=2)=CC=CC(Br)=C1 IUIFCWCDEZGVLL-LIRRHRJNSA-N 0.000 claims description 2
• BNPIELKFNYKKES-KUHUBIRLSA-N (5s)-5-(4-bromophenyl)-7-[(1r)-1-phenylethyl]-5,8-dihydroimidazo[1,5-a]pyrazin-6-one Chemical compound C1([C@@H]2N3C=NC=C3CN(C2=O)[C@H](C)C=2C=CC=CC=2)=CC=C(Br)C=C1 BNPIELKFNYKKES-KUHUBIRLSA-N 0.000 claims description 2
• BNPIELKFNYKKES-LIRRHRJNSA-N (5s)-5-(4-bromophenyl)-7-[(1s)-1-phenylethyl]-5,8-dihydroimidazo[1,5-a]pyrazin-6-one Chemical compound C1([C@@H]2N3C=NC=C3CN(C2=O)[C@@H](C)C=2C=CC=CC=2)=CC=C(Br)C=C1 BNPIELKFNYKKES-LIRRHRJNSA-N 0.000 claims description 2
• 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 2
• WRKVACHBUWUICF-UHFFFAOYSA-N 3-[6-oxo-7-(2-phenylethyl)-5,8-dihydroimidazo[1,5-a]pyrazin-5-yl]benzonitrile Chemical compound N12C=NC=C2CN(CCC=2C=CC=CC=2)C(=O)C1C1=CC=CC(C#N)=C1 WRKVACHBUWUICF-UHFFFAOYSA-N 0.000 claims description 2
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