JP6779870B2 - 抗増殖性化合物及びその使用方法 - Google Patents
抗増殖性化合物及びその使用方法 Download PDFInfo
- Publication number
- JP6779870B2 JP6779870B2 JP2017522462A JP2017522462A JP6779870B2 JP 6779870 B2 JP6779870 B2 JP 6779870B2 JP 2017522462 A JP2017522462 A JP 2017522462A JP 2017522462 A JP2017522462 A JP 2017522462A JP 6779870 B2 JP6779870 B2 JP 6779870B2
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- JP
- Japan
- Prior art keywords
- methyl
- oxoisoindoline
- dioxopiperidine
- difluoro
- acetamide
- Prior art date
- 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.)
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- 150000001875 compounds Chemical class 0.000 title claims description 545
- 230000001028 anti-proliverative effect Effects 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 claims description 294
- 239000000203 mixture Substances 0.000 claims description 210
- 125000001188 haloalkyl group Chemical group 0.000 claims description 200
- 229910052739 hydrogen Inorganic materials 0.000 claims description 163
- 239000001257 hydrogen Substances 0.000 claims description 163
- 150000003839 salts Chemical class 0.000 claims description 160
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 claims description 154
- 125000005843 halogen group Chemical group 0.000 claims description 152
- 238000000034 method Methods 0.000 claims description 147
- 239000012453 solvate Substances 0.000 claims description 136
- 206010028980 Neoplasm Diseases 0.000 claims description 134
- 125000000623 heterocyclic group Chemical group 0.000 claims description 132
- 125000001424 substituent group Chemical group 0.000 claims description 124
- 239000013078 crystal Substances 0.000 claims description 116
- -1 Chloro, methyl Chemical group 0.000 claims description 115
- 150000002431 hydrogen Chemical class 0.000 claims description 99
- 125000003118 aryl group Chemical group 0.000 claims description 86
- 125000001072 heteroaryl group Chemical group 0.000 claims description 81
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 80
- 201000011510 cancer Diseases 0.000 claims description 78
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 74
- 125000003107 substituted aryl group Chemical group 0.000 claims description 68
- 125000003545 alkoxy group Chemical group 0.000 claims description 66
- 125000005346 substituted cycloalkyl group Chemical group 0.000 claims description 65
- 125000002947 alkylene group Chemical group 0.000 claims description 64
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 62
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 60
- UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 claims description 55
- 125000004450 alkenylene group Chemical group 0.000 claims description 51
- 208000031261 Acute myeloid leukaemia Diseases 0.000 claims description 48
- 208000033776 Myeloid Acute Leukemia Diseases 0.000 claims description 47
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims description 47
- 208000032839 leukemia Diseases 0.000 claims description 47
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 47
- 229910052760 oxygen Inorganic materials 0.000 claims description 47
- 229910052717 sulfur Inorganic materials 0.000 claims description 47
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 41
- 125000005842 heteroatom Chemical group 0.000 claims description 38
- 239000008194 pharmaceutical composition Substances 0.000 claims description 32
- 208000024893 Acute lymphoblastic leukemia Diseases 0.000 claims description 27
- 208000006664 Precursor Cell Lymphoblastic Leukemia-Lymphoma Diseases 0.000 claims description 27
- 239000013543 active substance Substances 0.000 claims description 27
- 208000014697 Acute lymphocytic leukaemia Diseases 0.000 claims description 25
- 239000002246 antineoplastic agent Substances 0.000 claims description 21
- 208000032791 BCR-ABL1 positive chronic myelogenous leukemia Diseases 0.000 claims description 20
- 230000000306 recurrent effect Effects 0.000 claims description 19
- 208000033761 Myelogenous Chronic BCR-ABL Positive Leukemia Diseases 0.000 claims description 17
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 17
- 208000010833 Chronic myeloid leukaemia Diseases 0.000 claims description 16
- 239000003795 chemical substances by application Substances 0.000 claims description 16
- 239000002904 solvent Substances 0.000 claims description 15
- 208000010839 B-cell chronic lymphocytic leukemia Diseases 0.000 claims description 11
- 229910052757 nitrogen Inorganic materials 0.000 claims description 11
- 230000001225 therapeutic effect Effects 0.000 claims description 11
- 102000004127 Cytokines Human genes 0.000 claims description 10
- 108090000695 Cytokines Proteins 0.000 claims description 10
- 238000006243 chemical reaction Methods 0.000 claims description 9
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims description 9
- 208000031422 Lymphocytic Chronic B-Cell Leukemia Diseases 0.000 claims description 7
- 239000002253 acid Substances 0.000 claims description 7
- 208000032852 chronic lymphocytic leukemia Diseases 0.000 claims description 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 7
- 238000011443 conventional therapy Methods 0.000 claims description 6
- 125000001153 fluoro group Chemical group F* 0.000 claims description 6
- 125000004076 pyridyl group Chemical group 0.000 claims description 6
- 229910052794 bromium Inorganic materials 0.000 claims description 5
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 5
- 125000003386 piperidinyl group Chemical group 0.000 claims description 5
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 claims description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 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
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 4
- 239000000427 antigen Substances 0.000 claims description 3
- 102000036639 antigens Human genes 0.000 claims description 3
- 108091007433 antigens Proteins 0.000 claims description 3
- 229940111134 coxibs Drugs 0.000 claims description 3
- 239000003255 cyclooxygenase 2 inhibitor Substances 0.000 claims description 3
- 125000004438 haloalkoxy group Chemical group 0.000 claims description 3
- 230000008569 process Effects 0.000 claims description 3
- 230000009467 reduction Effects 0.000 claims description 3
- 230000003319 supportive effect Effects 0.000 claims description 3
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 claims description 2
- 239000002955 immunomodulating agent Substances 0.000 claims description 2
- 229940121354 immunomodulator Drugs 0.000 claims description 2
- 229960003444 immunosuppressant agent Drugs 0.000 claims description 2
- 239000003018 immunosuppressive agent Substances 0.000 claims description 2
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 claims 86
- METKIMKYRPQLGS-UHFFFAOYSA-N atenolol Chemical compound CC(C)NCC(O)COC1=CC=C(CC(N)=O)C=C1 METKIMKYRPQLGS-UHFFFAOYSA-N 0.000 claims 28
- 125000004785 fluoromethoxy group Chemical group [H]C([H])(F)O* 0.000 claims 8
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical group CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims 6
- 125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 claims 6
- 230000002194 synthesizing effect Effects 0.000 claims 6
- PWBHUSLMHZLGRN-UHFFFAOYSA-N 2-(4-chlorophenyl)-N-[[2-(2,6-dioxopiperidin-3-yl)-1-oxo-3H-isoindol-5-yl]methyl]-2,2-difluoroacetamide Chemical compound ClC1=CC=C(C=C1)C(C(=O)NCC=1C=C2CN(C(C2=CC=1)=O)C1C(NC(CC1)=O)=O)(F)F PWBHUSLMHZLGRN-UHFFFAOYSA-N 0.000 claims 5
- PVOAHINGSUIXLS-UHFFFAOYSA-N 1-Methylpiperazine Chemical compound CN1CCNCC1 PVOAHINGSUIXLS-UHFFFAOYSA-N 0.000 claims 4
- ZLIBRCVWTYTMME-UHFFFAOYSA-N 2-(2-chlorophenyl)-N-[[2-(2,6-dioxopiperidin-3-yl)-1-oxo-3H-isoindol-5-yl]methyl]-2,2-difluoroacetamide Chemical compound ClC1=C(C=CC=C1)C(C(=O)NCC=1C=C2CN(C(C2=CC=1)=O)C1C(NC(CC1)=O)=O)(F)F ZLIBRCVWTYTMME-UHFFFAOYSA-N 0.000 claims 4
- XLONUSFDGBQNQO-UHFFFAOYSA-N 2-(3-chlorophenyl)-N-[[2-(2,6-dioxopiperidin-3-yl)-1-oxo-3H-isoindol-5-yl]methyl]-2,2-difluoroacetamide Chemical compound ClC=1C=C(C=CC=1)C(C(=O)NCC=1C=C2CN(C(C2=CC=1)=O)C1C(NC(CC1)=O)=O)(F)F XLONUSFDGBQNQO-UHFFFAOYSA-N 0.000 claims 4
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 3
- 125000004215 2,4-difluorophenyl group Chemical group [H]C1=C([H])C(*)=C(F)C([H])=C1F 0.000 claims 2
- NCGYEIAZOMELDK-UHFFFAOYSA-N 2-(2,4-dichlorophenyl)-N-[[2-(2,6-dioxopiperidin-3-yl)-1-oxo-3H-isoindol-5-yl]methyl]-2,2-difluoroacetamide Chemical compound ClC1=C(C=CC(=C1)Cl)C(C(=O)NCC=1C=C2CN(C(C2=CC=1)=O)C1C(NC(CC1)=O)=O)(F)F NCGYEIAZOMELDK-UHFFFAOYSA-N 0.000 claims 2
- AIHKQMOGDSBXOL-UHFFFAOYSA-N 2-(2-aminopyrimidin-4-yl)-N-[[2-(2,6-dioxopiperidin-3-yl)-1-oxo-3H-isoindol-5-yl]methyl]-2,2-difluoroacetamide Chemical compound NC1=NC=CC(=N1)C(C(=O)NCC=1C=C2CN(C(C2=CC=1)=O)C1C(NC(CC1)=O)=O)(F)F AIHKQMOGDSBXOL-UHFFFAOYSA-N 0.000 claims 2
- DQBFRGQHCCHNSG-UHFFFAOYSA-N 2-(2-aminopyrimidin-5-yl)-N-[[2-(2,6-dioxopiperidin-3-yl)-1-oxo-3H-isoindol-5-yl]methyl]-2,2-difluoroacetamide Chemical compound NC1=NC=C(C=N1)C(C(=O)NCC=1C=C2CN(C(C2=CC=1)=O)C1C(NC(CC1)=O)=O)(F)F DQBFRGQHCCHNSG-UHFFFAOYSA-N 0.000 claims 2
- VSAYDRGRUYEOAD-UHFFFAOYSA-N 2-(3,4-dichlorophenyl)-N-[[2-(2,6-dioxopiperidin-3-yl)-1-oxo-3H-isoindol-5-yl]methyl]-2,2-difluoroacetamide Chemical compound ClC=1C=C(C=CC=1Cl)C(C(=O)NCC=1C=C2CN(C(C2=CC=1)=O)C1C(NC(CC1)=O)=O)(F)F VSAYDRGRUYEOAD-UHFFFAOYSA-N 0.000 claims 2
- AMUVSIVTAOXJLA-UHFFFAOYSA-N 2-(3-chloro-2-methylphenyl)-N-[[2-(2,6-dioxopiperidin-3-yl)-1-oxo-3H-isoindol-5-yl]methyl]-2,2-difluoroacetamide Chemical compound ClC=1C(=C(C=CC=1)C(C(=O)NCC=1C=C2CN(C(C2=CC=1)=O)C1C(NC(CC1)=O)=O)(F)F)C AMUVSIVTAOXJLA-UHFFFAOYSA-N 0.000 claims 2
- DDMLCIFNORUQRL-UHFFFAOYSA-N 2-(3-chloro-4-fluorophenyl)-N-[[2-(2,6-dioxopiperidin-3-yl)-1-oxo-3H-isoindol-5-yl]methyl]-2,2-difluoroacetamide Chemical compound ClC=1C=C(C=CC=1F)C(C(=O)NCC=1C=C2CN(C(C2=CC=1)=O)C1C(NC(CC1)=O)=O)(F)F DDMLCIFNORUQRL-UHFFFAOYSA-N 0.000 claims 2
- JFNYNFDROJUTRW-UHFFFAOYSA-N 2-(3-chloro-4-methoxyphenyl)-N-[[2-(2,6-dioxopiperidin-3-yl)-1-oxo-3H-isoindol-5-yl]methyl]-2,2-difluoroacetamide Chemical compound ClC=1C=C(C=CC=1OC)C(C(=O)NCC=1C=C2CN(C(C2=CC=1)=O)C1C(NC(CC1)=O)=O)(F)F JFNYNFDROJUTRW-UHFFFAOYSA-N 0.000 claims 2
- NYOULAILGSKVMS-UHFFFAOYSA-N 2-(3-chloro-4-methylphenyl)-N-[[2-(2,6-dioxopiperidin-3-yl)-1-oxo-3H-isoindol-5-yl]methyl]-2,2-difluoroacetamide Chemical compound ClC=1C=C(C=CC=1C)C(C(=O)NCC=1C=C2CN(C(C2=CC=1)=O)C1C(NC(CC1)=O)=O)(F)F NYOULAILGSKVMS-UHFFFAOYSA-N 0.000 claims 2
- DHJTVBVPHLKVMI-UHFFFAOYSA-N 2-(3-chloro-4-propan-2-yloxyphenyl)-N-[[2-(2,6-dioxopiperidin-3-yl)-1-oxo-3H-isoindol-5-yl]methyl]-2,2-difluoroacetamide Chemical compound ClC=1C=C(C=CC=1OC(C)C)C(C(=O)NCC=1C=C2CN(C(C2=CC=1)=O)C1C(NC(CC1)=O)=O)(F)F DHJTVBVPHLKVMI-UHFFFAOYSA-N 0.000 claims 2
- UXOHQYKAUVRSGR-UHFFFAOYSA-N 2-(4-bromophenyl)-N-[[2-(2,6-dioxopiperidin-3-yl)-1-oxo-3H-isoindol-5-yl]methyl]-2,2-difluoroacetamide Chemical compound BrC1=CC=C(C=C1)C(C(=O)NCC=1C=C2CN(C(C2=CC=1)=O)C1C(NC(CC1)=O)=O)(F)F UXOHQYKAUVRSGR-UHFFFAOYSA-N 0.000 claims 2
- TVRYUBFEWGXSHE-UHFFFAOYSA-N 2-(4-chloro-2-ethoxyphenyl)-N-[[2-(2,6-dioxopiperidin-3-yl)-1-oxo-3H-isoindol-5-yl]methyl]-2,2-difluoroacetamide Chemical compound ClC1=CC(=C(C=C1)C(C(=O)NCC=1C=C2CN(C(C2=CC=1)=O)C1C(NC(CC1)=O)=O)(F)F)OCC TVRYUBFEWGXSHE-UHFFFAOYSA-N 0.000 claims 2
- BEUXWCQJDJUWKP-UHFFFAOYSA-N 2-(4-chloro-2-methylphenyl)-N-[[2-(2,6-dioxopiperidin-3-yl)-1-oxo-3H-isoindol-5-yl]methyl]-2,2-difluoroacetamide Chemical compound ClC1=CC(=C(C=C1)C(C(=O)NCC=1C=C2CN(C(C2=CC=1)=O)C1C(NC(CC1)=O)=O)(F)F)C BEUXWCQJDJUWKP-UHFFFAOYSA-N 0.000 claims 2
- KZCJVXJRANKAGX-UHFFFAOYSA-N 2-(4-chloro-3-fluorophenyl)-N-[[2-(2,6-dioxopiperidin-3-yl)-1-oxo-3H-isoindol-5-yl]methyl]-2,2-difluoroacetamide Chemical compound ClC1=C(C=C(C=C1)C(C(=O)NCC=1C=C2CN(C(C2=CC=1)=O)C1C(NC(CC1)=O)=O)(F)F)F KZCJVXJRANKAGX-UHFFFAOYSA-N 0.000 claims 2
- XXOZRQAXDWOASO-UHFFFAOYSA-N 2-(4-cyclopropylphenyl)-N-[[2-(2,6-dioxopiperidin-3-yl)-1-oxo-3H-isoindol-5-yl]methyl]-2,2-difluoroacetamide Chemical compound C1(CC1)C1=CC=C(C=C1)C(C(=O)NCC=1C=C2CN(C(C2=CC=1)=O)C1C(NC(CC1)=O)=O)(F)F XXOZRQAXDWOASO-UHFFFAOYSA-N 0.000 claims 2
- PBXOPAYJJVDLNM-UHFFFAOYSA-N 2-(4-tert-butylphenyl)-N-[[2-(2,6-dioxopiperidin-3-yl)-1-oxo-3H-isoindol-5-yl]methyl]-2,2-difluoroacetamide Chemical compound C(C)(C)(C)C1=CC=C(C=C1)C(C(=O)NCC=1C=C2CN(C(C2=CC=1)=O)C1C(NC(CC1)=O)=O)(F)F PBXOPAYJJVDLNM-UHFFFAOYSA-N 0.000 claims 2
- KHOFGXWGIVOQDL-UHFFFAOYSA-N 2-(5-bromopyridin-2-yl)-N-[[2-(2,6-dioxopiperidin-3-yl)-1-oxo-3H-isoindol-5-yl]methyl]-2,2-difluoroacetamide Chemical compound BrC=1C=CC(=NC=1)C(C(=O)NCC=1C=C2CN(C(C2=CC=1)=O)C1C(NC(CC1)=O)=O)(F)F KHOFGXWGIVOQDL-UHFFFAOYSA-N 0.000 claims 2
- IFHGNGPDPXZMPD-UHFFFAOYSA-N 2-(5-chloropyridin-2-yl)-N-[[2-(2,6-dioxopiperidin-3-yl)-1-oxo-3H-isoindol-5-yl]methyl]-2,2-difluoroacetamide Chemical compound ClC=1C=CC(=NC=1)C(C(=O)NCC=1C=C2CN(C(C2=CC=1)=O)C1C(NC(CC1)=O)=O)(F)F IFHGNGPDPXZMPD-UHFFFAOYSA-N 0.000 claims 2
- BLUVQMUHGZOMQM-UHFFFAOYSA-N 2-(5-cyclopropylpyridin-2-yl)-N-[[2-(2,6-dioxopiperidin-3-yl)-1-oxo-3H-isoindol-5-yl]methyl]-2,2-difluoroacetamide Chemical compound C1(CC1)C=1C=CC(=NC=1)C(C(=O)NCC=1C=C2CN(C(C2=CC=1)=O)C1C(NC(CC1)=O)=O)(F)F BLUVQMUHGZOMQM-UHFFFAOYSA-N 0.000 claims 2
- GMHBAETVCYHAFR-UHFFFAOYSA-N 2-(5-tert-butylpyridin-2-yl)-N-[[2-(2,6-dioxopiperidin-3-yl)-1-oxo-3H-isoindol-5-yl]methyl]-2,2-difluoroacetamide Chemical compound C(C)(C)(C)C=1C=CC(=NC=1)C(C(=O)NCC=1C=C2CN(C(C2=CC=1)=O)C1C(NC(CC1)=O)=O)(F)F GMHBAETVCYHAFR-UHFFFAOYSA-N 0.000 claims 2
- VZXULRDQFRXODC-UHFFFAOYSA-N 2-[3-[2-(dimethylamino)ethoxy]phenyl]-N-[[2-(2,6-dioxopiperidin-3-yl)-1-oxo-3H-isoindol-5-yl]methyl]-2,2-difluoroacetamide Chemical compound CN(CCOC=1C=C(C=CC=1)C(C(=O)NCC=1C=C2CN(C(C2=CC=1)=O)C1C(NC(CC1)=O)=O)(F)F)C VZXULRDQFRXODC-UHFFFAOYSA-N 0.000 claims 2
- FAAWXONVJKBBDX-UHFFFAOYSA-N 2-[3-bromo-4-(trifluoromethoxy)phenyl]-N-[[2-(2,6-dioxopiperidin-3-yl)-1-oxo-3H-isoindol-5-yl]methyl]-2,2-difluoroacetamide Chemical compound BrC=1C=C(C=CC=1OC(F)(F)F)C(C(=O)NCC=1C=C2CN(C(C2=CC=1)=O)C1C(NC(CC1)=O)=O)(F)F FAAWXONVJKBBDX-UHFFFAOYSA-N 0.000 claims 2
- ALYVPCSTUSYUPW-UHFFFAOYSA-N 2-[3-chloro-4-(trifluoromethoxy)phenyl]-N-[[2-(2,6-dioxopiperidin-3-yl)-1-oxo-3H-isoindol-5-yl]methyl]-2,2-difluoroacetamide Chemical compound ClC=1C=C(C=CC=1OC(F)(F)F)C(C(=O)NCC=1C=C2CN(C(C2=CC=1)=O)C1C(NC(CC1)=O)=O)(F)F ALYVPCSTUSYUPW-UHFFFAOYSA-N 0.000 claims 2
- JTODFZWZPZGMBU-UHFFFAOYSA-N 2-[4-chloro-2-(trifluoromethoxy)phenyl]-N-[[2-(2,6-dioxopiperidin-3-yl)-1-oxo-3H-isoindol-5-yl]methyl]-2,2-difluoroacetamide Chemical compound ClC1=CC(=C(C=C1)C(C(=O)NCC=1C=C2CN(C(C2=CC=1)=O)C1C(NC(CC1)=O)=O)(F)F)OC(F)(F)F JTODFZWZPZGMBU-UHFFFAOYSA-N 0.000 claims 2
- MZMQDTGOAVTIRS-UHFFFAOYSA-N 2-[4-chloro-2-(trifluoromethyl)phenyl]-N-[[2-(2,6-dioxopiperidin-3-yl)-1-oxo-3H-isoindol-5-yl]methyl]-2,2-difluoroacetamide Chemical compound ClC1=CC(=C(C=C1)C(C(=O)NCC=1C=C2CN(C(C2=CC=1)=O)C1C(NC(CC1)=O)=O)(F)F)C(F)(F)F MZMQDTGOAVTIRS-UHFFFAOYSA-N 0.000 claims 2
- WPBYBHMGNDQPDI-UHFFFAOYSA-N 2-cyclohexyl-N-[[2-(2,6-dioxopiperidin-3-yl)-1-oxo-3H-isoindol-5-yl]methyl]-2,2-difluoroacetamide Chemical compound C1(CCCCC1)C(C(=O)NCC=1C=C2CN(C(C2=CC=1)=O)C1C(NC(CC1)=O)=O)(F)F WPBYBHMGNDQPDI-UHFFFAOYSA-N 0.000 claims 2
- SQMHSDLOEJOJIL-UHFFFAOYSA-N 2-cyclopentyl-N-[[2-(2,6-dioxopiperidin-3-yl)-1-oxo-3H-isoindol-5-yl]methyl]-2,2-difluoroacetamide Chemical compound C1(CCCC1)C(C(=O)NCC=1C=C2CN(C(C2=CC=1)=O)C1C(NC(CC1)=O)=O)(F)F SQMHSDLOEJOJIL-UHFFFAOYSA-N 0.000 claims 2
- PRNZBCYBKGCOFI-UHFFFAOYSA-N 2-fluoropropane Chemical compound CC(C)F PRNZBCYBKGCOFI-UHFFFAOYSA-N 0.000 claims 2
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Classifications
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- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
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- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
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- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/501—Pyridazines; Hydrogenated pyridazines not condensed and containing further heterocyclic rings
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- C07D—HETEROCYCLIC COMPOUNDS
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- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
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Publication number | Priority date | Publication date | Assignee | Title |
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JP2019502708A (ja) * | 2016-01-08 | 2019-01-31 | セルジーン コーポレイション | 2−(4−クロロフェニル)−n−((2−(2,6−ジオキソピペリジン−3−イル)−1−オキソイソインドリン−5−イル)メチル)−2,2−ジフルオロアセトアミドの固体形態、ならびにそれらの薬学的組成物及び使用 |
JP7071922B2 (ja) | 2016-01-08 | 2022-05-19 | セルジーン コーポレイション | 2-(4-クロロフェニル)-n-((2-(2,6-ジオキソピペリジン-3-イル)-1-オキソイソインドリン-5-イル)メチル)-2,2-ジフルオロアセトアミドの固体形態、ならびにそれらの薬学的組成物及び使用 |
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