JP5992054B2 - ピラゾロピロリジン化合物 - Google Patents

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Publication number

JP5992054B2

JP5992054B2 JP2014544018A JP2014544018A JP5992054B2 JP 5992054 B2 JP5992054 B2 JP 5992054B2 JP 2014544018 A JP2014544018 A JP 2014544018A JP 2014544018 A JP2014544018 A JP 2014544018A JP 5992054 B2 JP5992054 B2 JP 5992054B2

Authority

JP

Japan

Prior art keywords

chloro

phenyl

methyl

dihydro

pyrazol

Prior art date

2011-11-29

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 - Fee Related

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• -1 Pyrazolopyrrolidine compound Chemical class 0.000 title claims description 198
• 150000001875 compounds Chemical class 0.000 claims description 540
• 125000000217 alkyl group Chemical group 0.000 claims description 156
• 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 72
• 108050002772 E3 ubiquitin-protein ligase Mdm2 Proteins 0.000 claims description 71
• 102000012199 E3 ubiquitin-protein ligase Mdm2 Human genes 0.000 claims description 70
• 230000000694 effects Effects 0.000 claims description 68
• 150000003839 salts Chemical class 0.000 claims description 67
• 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 63
• 125000001424 substituent group Chemical group 0.000 claims description 63
• XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 62
• 125000005843 halogen group Chemical group 0.000 claims description 51
• 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 51
• 108050005300 MDM4 Proteins 0.000 claims description 46
• 102000017274 MDM4 Human genes 0.000 claims description 46
• 125000000623 heterocyclic group Chemical group 0.000 claims description 42
• 201000010099 disease Diseases 0.000 claims description 41
• 229920006395 saturated elastomer Polymers 0.000 claims description 40
• 125000004093 cyano group Chemical group *C#N 0.000 claims description 36
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 36
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 36
• 125000003545 alkoxy group Chemical group 0.000 claims description 34
• 238000011282 treatment Methods 0.000 claims description 34
• 239000003814 drug Substances 0.000 claims description 33
• 239000008194 pharmaceutical composition Substances 0.000 claims description 24
• 208000035475 disorder Diseases 0.000 claims description 22
• JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Substances N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 claims description 19
• 125000001072 heteroaryl group Chemical group 0.000 claims description 19
• 230000001404 mediated effect Effects 0.000 claims description 17
• 229910052799 carbon Inorganic materials 0.000 claims description 16
• 125000001153 fluoro group Chemical group F* 0.000 claims description 15
• 125000005842 heteroatom Chemical group 0.000 claims description 15
• 125000002950 monocyclic group Chemical group 0.000 claims description 15
• 229910052760 oxygen Inorganic materials 0.000 claims description 14
• 229910052717 sulfur Inorganic materials 0.000 claims description 13
• 125000000753 cycloalkyl group Chemical group 0.000 claims description 12
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 12
• 125000005037 alkyl phenyl group Chemical group 0.000 claims description 11
• 150000001721 carbon Chemical group 0.000 claims description 11
• 125000005213 alkyl heteroaryl group Chemical group 0.000 claims description 10
• 125000004204 2-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C(OC([H])([H])[H])C([H])=C1[H] 0.000 claims description 9
• 125000001309 chloro group Chemical group Cl* 0.000 claims description 9
• 125000004528 pyrimidin-5-yl group Chemical group N1=CN=CC(=C1)* 0.000 claims description 9
• OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 8
• AYJVXDFOPGRLNI-QHCPKHFHSA-N (4s)-5-(5-chloro-1-methyl-6-oxopyridin-3-yl)-4-(4-chloro-2-methylphenyl)-2-(2,4-dimethoxypyrimidin-5-yl)-3-propan-2-yl-4h-pyrrolo[3,4-c]pyrazol-6-one Chemical compound COC1=NC(OC)=NC=C1N1C(C(C)C)=C2[C@H](C=3C(=CC(Cl)=CC=3)C)N(C3=CN(C)C(=O)C(Cl)=C3)C(=O)C2=N1 AYJVXDFOPGRLNI-QHCPKHFHSA-N 0.000 claims description 7
• 125000004434 sulfur atom Chemical group 0.000 claims description 7
• RQRGUXOSYRMAOC-DEOSSOPVSA-N 4-[(4s)-5-(5-chloro-1-methyl-6-oxopyridin-3-yl)-2-[2-(dimethylamino)-4-methoxypyrimidin-5-yl]-6-oxo-3-propan-2-yl-4h-pyrrolo[3,4-c]pyrazol-4-yl]benzonitrile Chemical compound COC1=NC(N(C)C)=NC=C1N1C(C(C)C)=C2[C@H](C=3C=CC(=CC=3)C#N)N(C3=CN(C)C(=O)C(Cl)=C3)C(=O)C2=N1 RQRGUXOSYRMAOC-DEOSSOPVSA-N 0.000 claims description 6
• IDRGFNPZDVBSSE-UHFFFAOYSA-N OCCN1CCN(CC1)c1ccc(Nc2ncc3cccc(-c4cccc(NC(=O)C=C)c4)c3n2)c(F)c1F Chemical compound OCCN1CCN(CC1)c1ccc(Nc2ncc3cccc(-c4cccc(NC(=O)C=C)c4)c3n2)c(F)c1F IDRGFNPZDVBSSE-UHFFFAOYSA-N 0.000 claims description 6
• 125000003342 alkenyl group Chemical group 0.000 claims description 6
• 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 6
• 238000004519 manufacturing process Methods 0.000 claims description 6
• 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 6
• IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 6
• 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims description 5
• YDAUQLMQAVQZLU-UHFFFAOYSA-N 4-(4-chloro-3-fluorophenyl)-5-(5-chloro-1-methyl-6-oxopyridin-3-yl)-2-(2,4-dimethoxypyrimidin-5-yl)-3-propan-2-yl-4h-pyrrolo[3,4-c]pyrazol-6-one Chemical compound COC1=NC(OC)=NC=C1N1C(C(C)C)=C2C(C=3C=C(F)C(Cl)=CC=3)N(C3=CN(C)C(=O)C(Cl)=C3)C(=O)C2=N1 YDAUQLMQAVQZLU-UHFFFAOYSA-N 0.000 claims description 5
• RQRGUXOSYRMAOC-UHFFFAOYSA-N 4-[5-(5-chloro-1-methyl-6-oxopyridin-3-yl)-2-[2-(dimethylamino)-4-methoxypyrimidin-5-yl]-6-oxo-3-propan-2-yl-4h-pyrrolo[3,4-c]pyrazol-4-yl]benzonitrile Chemical compound COC1=NC(N(C)C)=NC=C1N1C(C(C)C)=C2C(C=3C=CC(=CC=3)C#N)N(C3=CN(C)C(=O)C(Cl)=C3)C(=O)C2=N1 RQRGUXOSYRMAOC-UHFFFAOYSA-N 0.000 claims description 5
• AYJVXDFOPGRLNI-UHFFFAOYSA-N 5-(5-chloro-1-methyl-6-oxopyridin-3-yl)-4-(4-chloro-2-methylphenyl)-2-(2,4-dimethoxypyrimidin-5-yl)-3-propan-2-yl-4h-pyrrolo[3,4-c]pyrazol-6-one Chemical compound COC1=NC(OC)=NC=C1N1C(C(C)C)=C2C(C=3C(=CC(Cl)=CC=3)C)N(C3=CN(C)C(=O)C(Cl)=C3)C(=O)C2=N1 AYJVXDFOPGRLNI-UHFFFAOYSA-N 0.000 claims description 5
• OIFYSZRTTNMVQD-UHFFFAOYSA-N 5-(5-chloro-2-oxo-1h-pyridin-3-yl)-4-(4-chlorophenyl)-2-(2,4-dimethoxypyrimidin-5-yl)-3-propan-2-yl-4h-pyrrolo[3,4-c]pyrazol-6-one Chemical compound COC1=NC(OC)=NC=C1N1C(C(C)C)=C2C(C=3C=CC(Cl)=CC=3)N(C=3C(NC=C(Cl)C=3)=O)C(=O)C2=N1 OIFYSZRTTNMVQD-UHFFFAOYSA-N 0.000 claims description 5
• IRPVABHDSJVBNZ-RTHVDDQRSA-N 5-[1-(cyclopropylmethyl)-5-[(1R,5S)-3-(oxetan-3-yl)-3-azabicyclo[3.1.0]hexan-6-yl]pyrazol-3-yl]-3-(trifluoromethyl)pyridin-2-amine Chemical compound C1=C(C(F)(F)F)C(N)=NC=C1C1=NN(CC2CC2)C(C2[C@@H]3CN(C[C@@H]32)C2COC2)=C1 IRPVABHDSJVBNZ-RTHVDDQRSA-N 0.000 claims description 5
• 125000002619 bicyclic group Chemical group 0.000 claims description 5
• 239000003937 drug carrier Substances 0.000 claims description 5
• 229910052757 nitrogen Inorganic materials 0.000 claims description 5
• 125000004430 oxygen atom Chemical group O* 0.000 claims description 5
• RSRIVJZZBKJDKL-UHFFFAOYSA-N 4-[5-(5-chloro-1-methyl-6-oxopyridin-3-yl)-2-(2,4-dimethoxypyrimidin-5-yl)-6-oxo-3-propan-2-yl-4h-pyrrolo[3,4-c]pyrazol-4-yl]-3-fluorobenzonitrile Chemical compound COC1=NC(OC)=NC=C1N1C(C(C)C)=C2C(C=3C(=CC(=CC=3)C#N)F)N(C3=CN(C)C(=O)C(Cl)=C3)C(=O)C2=N1 RSRIVJZZBKJDKL-UHFFFAOYSA-N 0.000 claims description 4
• 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 4
• 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 4
• QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 4
• 238000006467 substitution reaction Methods 0.000 claims description 4
• 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 4
• YOXSWOWVTGKRRI-XYXHBKGXSA-N (2s)-2-[[4-(4-chloro-2-methylphenyl)-5-(5-chloro-2-methylphenyl)-6-oxo-3-propan-2-yl-4h-pyrrolo[3,4-c]pyrazol-2-yl]methyl]-n,n-dimethylpyrrolidine-1-carboxamide Chemical compound CC(C)C1=C2C(C=3C(=CC(Cl)=CC=3)C)N(C=3C(=CC=C(Cl)C=3)C)C(=O)C2=NN1C[C@@H]1CCCN1C(=O)N(C)C YOXSWOWVTGKRRI-XYXHBKGXSA-N 0.000 claims description 3
• MAYZWDRUFKUGGP-VIFPVBQESA-N (3s)-1-[5-tert-butyl-3-[(1-methyltetrazol-5-yl)methyl]triazolo[4,5-d]pyrimidin-7-yl]pyrrolidin-3-ol Chemical compound CN1N=NN=C1CN1C2=NC(C(C)(C)C)=NC(N3C[C@@H](O)CC3)=C2N=N1 MAYZWDRUFKUGGP-VIFPVBQESA-N 0.000 claims description 3
• SJSSRJQZFGJFOX-QFIPXVFZSA-N (4s)-5-(5-chloro-2-oxo-1h-pyridin-3-yl)-4-(4-chlorophenyl)-2-[2-(dimethylamino)-4-methoxypyrimidin-5-yl]-3-propan-2-yl-4h-pyrrolo[3,4-c]pyrazol-6-one Chemical compound COC1=NC(N(C)C)=NC=C1N1C(C(C)C)=C2[C@H](C=3C=CC(Cl)=CC=3)N(C=3C(NC=C(Cl)C=3)=O)C(=O)C2=N1 SJSSRJQZFGJFOX-QFIPXVFZSA-N 0.000 claims description 3
• ZGYIXVSQHOKQRZ-COIATFDQSA-N (e)-n-[4-[3-chloro-4-(pyridin-2-ylmethoxy)anilino]-3-cyano-7-[(3s)-oxolan-3-yl]oxyquinolin-6-yl]-4-(dimethylamino)but-2-enamide Chemical compound N#CC1=CN=C2C=C(O[C@@H]3COCC3)C(NC(=O)/C=C/CN(C)C)=CC2=C1NC(C=C1Cl)=CC=C1OCC1=CC=CC=N1 ZGYIXVSQHOKQRZ-COIATFDQSA-N 0.000 claims description 3
• DZWXCJZDTKKTNU-UHFFFAOYSA-N 2-[(1-acetyl-4-hydroxypiperidin-4-yl)methyl]-4-(4-chloro-2-methylphenyl)-5-(5-chloro-2-methylphenyl)-3-propan-2-yl-4h-pyrrolo[3,4-c]pyrazol-6-one Chemical compound CC(C)C1=C2C(C=3C(=CC(Cl)=CC=3)C)N(C=3C(=CC=C(Cl)C=3)C)C(=O)C2=NN1CC1(O)CCN(C(C)=O)CC1 DZWXCJZDTKKTNU-UHFFFAOYSA-N 0.000 claims description 3
• QZPHTHGRGSOROE-UHFFFAOYSA-N 2-[(1-acetylpiperidin-4-yl)methyl]-4-(4-chloro-2-methylphenyl)-5-(5-chloro-2-methylphenyl)-3-propan-2-yl-4h-pyrrolo[3,4-c]pyrazol-6-one Chemical compound CC(C)C1=C2C(C=3C(=CC(Cl)=CC=3)C)N(C=3C(=CC=C(Cl)C=3)C)C(=O)C2=NN1CC1CCN(C(C)=O)CC1 QZPHTHGRGSOROE-UHFFFAOYSA-N 0.000 claims description 3
• YBBQYZSRNHSUCI-UHFFFAOYSA-N 2-[2-(4-acetylpiperazin-1-yl)-2-oxoethyl]-4-(4-chloro-2-methylphenyl)-5-(5-chloro-2-methylphenyl)-3-propan-2-yl-4h-pyrrolo[3,4-c]pyrazol-6-one Chemical compound CC(C)C1=C2C(C=3C(=CC(Cl)=CC=3)C)N(C=3C(=CC=C(Cl)C=3)C)C(=O)C2=NN1CC(=O)N1CCN(C(C)=O)CC1 YBBQYZSRNHSUCI-UHFFFAOYSA-N 0.000 claims description 3
• IQXKRKFNNIJHKM-UHFFFAOYSA-N 2-[2-[5-(3-chloro-2-fluorophenyl)-4-(4-chloro-2-methylphenyl)-6-oxo-3-propan-2-yl-4h-pyrrolo[3,4-c]pyrazol-2-yl]ethyl]isoindole-1,3-dione Chemical compound O=C1C2=NN(CCN3C(C4=CC=CC=C4C3=O)=O)C(C(C)C)=C2C(C=2C(=CC(Cl)=CC=2)C)N1C1=CC=CC(Cl)=C1F IQXKRKFNNIJHKM-UHFFFAOYSA-N 0.000 claims description 3
• YEQFUJXHFVNFLD-UHFFFAOYSA-N 2-[5-(3-chloro-2-fluorophenyl)-4-(4-chloro-2-methylphenyl)-6-oxo-3-propan-2-yl-4h-pyrrolo[3,4-c]pyrazol-2-yl]-n-methylacetamide Chemical compound C12=C(C(C)C)N(CC(=O)NC)N=C2C(=O)N(C=2C(=C(Cl)C=CC=2)F)C1C1=CC=C(Cl)C=C1C YEQFUJXHFVNFLD-UHFFFAOYSA-N 0.000 claims description 3
• JZFAHAGJOFEDPR-XYXHBKGXSA-N 2-[[(2s)-1-acetylpyrrolidin-2-yl]methyl]-4-(4-chloro-2-methylphenyl)-5-(5-chloro-2-methylphenyl)-3-propan-2-yl-4h-pyrrolo[3,4-c]pyrazol-6-one Chemical compound CC(C)C1=C2C(C=3C(=CC(Cl)=CC=3)C)N(C=3C(=CC=C(Cl)C=3)C)C(=O)C2=NN1C[C@@H]1CCCN1C(C)=O JZFAHAGJOFEDPR-XYXHBKGXSA-N 0.000 claims description 3
• KQFUYAPAPGFYMI-UHFFFAOYSA-N 2-[[4-(4-chlorophenyl)-5-(3,4-difluorophenyl)-6-oxo-3-propan-2-yl-4h-pyrrolo[3,4-c]pyrazol-2-yl]methyl]benzonitrile Chemical compound CC(C)C1=C2C(C=3C=CC(Cl)=CC=3)N(C=3C=C(F)C(F)=CC=3)C(=O)C2=NN1CC1=CC=CC=C1C#N KQFUYAPAPGFYMI-UHFFFAOYSA-N 0.000 claims description 3
• AVTJOXSIUYDNFU-UHFFFAOYSA-N 2-benzyl-4-(4-chloro-2-methylphenyl)-5-(5-chloro-2-methylphenyl)-3-propan-2-yl-4h-pyrrolo[3,4-c]pyrazol-6-one Chemical compound CC(C)C1=C2C(C=3C(=CC(Cl)=CC=3)C)N(C=3C(=CC=C(Cl)C=3)C)C(=O)C2=NN1CC1=CC=CC=C1 AVTJOXSIUYDNFU-UHFFFAOYSA-N 0.000 claims description 3
• WPSSCIDRUBTKAN-UHFFFAOYSA-N 2-benzyl-5-(3-chloro-2-fluorophenyl)-4-(4-chloro-2-methylphenyl)-3-propan-2-yl-4h-pyrrolo[3,4-c]pyrazol-6-one Chemical compound CC(C)C1=C2C(C=3C(=CC(Cl)=CC=3)C)N(C=3C(=C(Cl)C=CC=3)F)C(=O)C2=NN1CC1=CC=CC=C1 WPSSCIDRUBTKAN-UHFFFAOYSA-N 0.000 claims description 3
• GNUPSFNBJBWYRB-UHFFFAOYSA-N 4-(4-chloro-2-methylphenyl)-5-(5-chloro-2-methylphenyl)-2-(1-methylpiperidin-4-yl)-3-propan-2-yl-4h-pyrrolo[3,4-c]pyrazol-6-one Chemical compound CC(C)C1=C2C(C=3C(=CC(Cl)=CC=3)C)N(C=3C(=CC=C(Cl)C=3)C)C(=O)C2=NN1C1CCN(C)CC1 GNUPSFNBJBWYRB-UHFFFAOYSA-N 0.000 claims description 3
• HWOBQJWTOBDSQY-UHFFFAOYSA-N 4-(4-chloro-2-methylphenyl)-5-(5-chloro-2-methylphenyl)-2-(2,3-dihydroxypropyl)-3-propan-2-yl-4h-pyrrolo[3,4-c]pyrazol-6-one Chemical compound O=C1C2=NN(CC(O)CO)C(C(C)C)=C2C(C=2C(=CC(Cl)=CC=2)C)N1C1=CC(Cl)=CC=C1C HWOBQJWTOBDSQY-UHFFFAOYSA-N 0.000 claims description 3
• VWMHDGDJQMBFHU-UHFFFAOYSA-N 4-(4-chloro-2-methylphenyl)-5-(5-chloro-2-methylphenyl)-2-(2-methoxyethyl)-3-propan-2-yl-4h-pyrrolo[3,4-c]pyrazol-6-one Chemical compound C12=C(C(C)C)N(CCOC)N=C2C(=O)N(C=2C(=CC=C(Cl)C=2)C)C1C1=CC=C(Cl)C=C1C VWMHDGDJQMBFHU-UHFFFAOYSA-N 0.000 claims description 3
• MVJPAODGJWVCNG-UHFFFAOYSA-N 4-(4-chloro-2-methylphenyl)-5-(5-chloro-2-methylphenyl)-2-(4-methylpiperazine-1-carbonyl)-3-propan-2-yl-4h-pyrrolo[3,4-c]pyrazol-6-one Chemical compound CC(C)C1=C2C(C=3C(=CC(Cl)=CC=3)C)N(C=3C(=CC=C(Cl)C=3)C)C(=O)C2=NN1C(=O)N1CCN(C)CC1 MVJPAODGJWVCNG-UHFFFAOYSA-N 0.000 claims description 3
• BSYBXKOGLZBSHD-UHFFFAOYSA-N 4-(4-chloro-2-methylphenyl)-5-(5-chloro-2-methylphenyl)-2-(oxiran-2-ylmethyl)-3-propan-2-yl-4h-pyrrolo[3,4-c]pyrazol-6-one Chemical compound CC(C)C1=C2C(C=3C(=CC(Cl)=CC=3)C)N(C=3C(=CC=C(Cl)C=3)C)C(=O)C2=NN1CC1CO1 BSYBXKOGLZBSHD-UHFFFAOYSA-N 0.000 claims description 3
• KZKVSNXVFALSMC-UHFFFAOYSA-N 4-(4-chloro-2-methylphenyl)-5-(5-chloro-2-methylphenyl)-2-(oxolan-2-ylmethyl)-3-propan-2-yl-4h-pyrrolo[3,4-c]pyrazol-6-one Chemical compound CC(C)C1=C2C(C=3C(=CC(Cl)=CC=3)C)N(C=3C(=CC=C(Cl)C=3)C)C(=O)C2=NN1CC1CCCO1 KZKVSNXVFALSMC-UHFFFAOYSA-N 0.000 claims description 3
• IRWCMXNZTJROFT-UHFFFAOYSA-N 4-(4-chloro-2-methylphenyl)-5-(5-chloro-2-methylphenyl)-2-[2-(2-oxopyrrolidin-1-yl)ethyl]-3-propan-2-yl-4h-pyrrolo[3,4-c]pyrazol-6-one Chemical compound CC(C)C1=C2C(C=3C(=CC(Cl)=CC=3)C)N(C=3C(=CC=C(Cl)C=3)C)C(=O)C2=NN1CCN1CCCC1=O IRWCMXNZTJROFT-UHFFFAOYSA-N 0.000 claims description 3
• IIZXQQZRRXYLSE-UHFFFAOYSA-N 4-(4-chloro-2-methylphenyl)-5-(5-chloro-2-methylphenyl)-2-[2-(4-hydroxypiperidin-1-yl)-2-oxoethyl]-3-propan-2-yl-4h-pyrrolo[3,4-c]pyrazol-6-one Chemical compound CC(C)C1=C2C(C=3C(=CC(Cl)=CC=3)C)N(C=3C(=CC=C(Cl)C=3)C)C(=O)C2=NN1CC(=O)N1CCC(O)CC1 IIZXQQZRRXYLSE-UHFFFAOYSA-N 0.000 claims description 3
• UNZCOOAPYFTFKR-UHFFFAOYSA-N 4-(4-chloro-2-methylphenyl)-5-(5-chloro-2-methylphenyl)-2-[2-(4-methylpiperazin-1-yl)ethyl]-3-propan-2-yl-4h-pyrrolo[3,4-c]pyrazol-6-one Chemical compound CC(C)C1=C2C(C=3C(=CC(Cl)=CC=3)C)N(C=3C(=CC=C(Cl)C=3)C)C(=O)C2=NN1CCN1CCN(C)CC1 UNZCOOAPYFTFKR-UHFFFAOYSA-N 0.000 claims description 3
• DBEMYIHLOZGDDF-UHFFFAOYSA-N 4-(4-chloro-2-methylphenyl)-5-(5-chloro-2-methylphenyl)-2-[2-oxo-2-(3-oxopiperazin-1-yl)ethyl]-3-propan-2-yl-4h-pyrrolo[3,4-c]pyrazol-6-one Chemical compound CC(C)C1=C2C(C=3C(=CC(Cl)=CC=3)C)N(C=3C(=CC=C(Cl)C=3)C)C(=O)C2=NN1CC(=O)N1CCNC(=O)C1 DBEMYIHLOZGDDF-UHFFFAOYSA-N 0.000 claims description 3
• PSCSHVNMQAGNHC-UHFFFAOYSA-N 4-(4-chloro-2-methylphenyl)-5-(5-chloro-2-methylphenyl)-3-propan-2-yl-2-(pyridin-2-ylmethyl)-4h-pyrrolo[3,4-c]pyrazol-6-one Chemical compound CC(C)C1=C2C(C=3C(=CC(Cl)=CC=3)C)N(C=3C(=CC=C(Cl)C=3)C)C(=O)C2=NN1CC1=CC=CC=N1 PSCSHVNMQAGNHC-UHFFFAOYSA-N 0.000 claims description 3
• YDPLGSFJBCHSDW-UHFFFAOYSA-N 4-(4-chloro-2-methylphenyl)-5-(5-chloro-2-methylphenyl)-n-methyl-6-oxo-n-phenyl-3-propan-2-yl-4h-pyrrolo[3,4-c]pyrazole-2-carboxamide Chemical compound CC(C)C1=C2C(C=3C(=CC(Cl)=CC=3)C)N(C=3C(=CC=C(Cl)C=3)C)C(=O)C2=NN1C(=O)N(C)C1=CC=CC=C1 YDPLGSFJBCHSDW-UHFFFAOYSA-N 0.000 claims description 3
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• XTRBDZDWKLQSPN-UHFFFAOYSA-N 5-(3-chloro-2-fluorophenyl)-4-(4-fluorophenyl)-2-(3-methylbutyl)-3-propan-2-yl-4h-pyrrolo[3,4-c]pyrazol-6-one Chemical compound C12=C(C(C)C)N(CCC(C)C)N=C2C(=O)N(C=2C(=C(Cl)C=CC=2)F)C1C1=CC=C(F)C=C1 XTRBDZDWKLQSPN-UHFFFAOYSA-N 0.000 claims description 3
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• 239000013543 active substance Substances 0.000 claims description 3
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• 125000001624 naphthyl group Chemical group 0.000 claims description 3
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• 125000006413 ring segment Chemical group 0.000 claims description 3
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