BRPI0813999A2 - ciclopentanos de pirimidil como inibidores de akt proteína cinase - Google Patents
ciclopentanos de pirimidil como inibidores de akt proteína cinase Download PDFInfo
- Publication number
- BRPI0813999A2 BRPI0813999A2 BRPI0813999A BRPI0813999A BRPI0813999A2 BR PI0813999 A2 BRPI0813999 A2 BR PI0813999A2 BR PI0813999 A BRPI0813999 A BR PI0813999A BR PI0813999 A BRPI0813999 A BR PI0813999A BR PI0813999 A2 BRPI0813999 A2 BR PI0813999A2
- Authority
- BR
- Brazil
- Prior art keywords
- pyrimidin
- ethanone
- piperazin
- dihydro
- methyl
- Prior art date
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- -1 pyrimidyl cyclopentanes Chemical class 0.000 title claims abstract 68
- 229940045988 antineoplastic drug protein kinase inhibitors Drugs 0.000 title abstract 3
- 239000003909 protein kinase inhibitor Substances 0.000 title abstract 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 11
- 201000010099 disease Diseases 0.000 claims abstract description 8
- 206010028980 Neoplasm Diseases 0.000 claims abstract description 5
- 201000011510 cancer Diseases 0.000 claims abstract description 4
- 230000003463 hyperproliferative effect Effects 0.000 claims abstract description 4
- 150000001875 compounds Chemical class 0.000 claims abstract 81
- 150000003839 salts Chemical class 0.000 claims abstract 8
- 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 abstract 3
- 239000008194 pharmaceutical composition Substances 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 6
- 241000124008 Mammalia Species 0.000 claims description 5
- 238000006243 chemical reaction Methods 0.000 claims description 3
- 208000035475 disorder Diseases 0.000 claims description 3
- 201000004681 Psoriasis Diseases 0.000 claims description 2
- 125000004194 piperazin-1-yl group Chemical group [H]N1C([H])([H])C([H])([H])N(*)C([H])([H])C1([H])[H] 0.000 claims 31
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 claims 21
- 125000000623 heterocyclic group Chemical group 0.000 claims 11
- 125000004527 pyrimidin-4-yl group Chemical group N1=CN=C(C=C1)* 0.000 claims 11
- 239000003814 drug Substances 0.000 claims 9
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims 9
- 230000001404 mediated effect Effects 0.000 claims 8
- 125000004429 atom Chemical group 0.000 claims 7
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims 6
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims 6
- 229940079593 drug Drugs 0.000 claims 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 6
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 claims 5
- 125000004800 4-bromophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Br 0.000 claims 4
- KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 claims 4
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims 4
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 4
- 238000004519 manufacturing process Methods 0.000 claims 4
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 4
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims 3
- 208000008770 Multiple Hamartoma Syndrome Diseases 0.000 claims 3
- 125000000217 alkyl group Chemical group 0.000 claims 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 3
- 229910052799 carbon Inorganic materials 0.000 claims 3
- 229910052736 halogen Inorganic materials 0.000 claims 3
- 150000002367 halogens Chemical class 0.000 claims 3
- 125000005842 heteroatom Chemical group 0.000 claims 3
- 125000004043 oxo group Chemical group O=* 0.000 claims 3
- AJAUYRZUZLBSAI-QEMXTEJRSA-N (2s)-1-[4-[(5r,7r)-7-methoxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]-2-[(2s)-pyrrolidin-2-yl]-2-[4-(trifluoromethyl)phenyl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C2=NC=NC3=C2[C@H](C)C[C@H]3OC)C=2C=CC(=CC=2)C(F)(F)F)CCN1 AJAUYRZUZLBSAI-QEMXTEJRSA-N 0.000 claims 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 2
- 125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 claims 2
- ICSNLGPSRYBMBD-UHFFFAOYSA-N 2-aminopyridine Chemical compound NC1=CC=CC=N1 ICSNLGPSRYBMBD-UHFFFAOYSA-N 0.000 claims 2
- 125000004189 3,4-dichlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(Cl)C([H])=C1* 0.000 claims 2
- 125000004801 4-cyanophenyl group Chemical group [H]C1=C([H])C(C#N)=C([H])C([H])=C1* 0.000 claims 2
- 125000004199 4-trifluoromethylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C(F)(F)F 0.000 claims 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 2
- AOJJSUZBOXZQNB-TZSSRYMLSA-N Doxorubicin Chemical compound O([C@H]1C[C@@](O)(CC=2C(O)=C3C(=O)C=4C=CC=C(C=4C(=O)C3=C(O)C=21)OC)C(=O)CO)[C@H]1C[C@H](N)[C@H](O)[C@H](C)O1 AOJJSUZBOXZQNB-TZSSRYMLSA-N 0.000 claims 2
- 208000031481 Pathologic Constriction Diseases 0.000 claims 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 2
- 238000010511 deprotection reaction Methods 0.000 claims 2
- 230000002401 inhibitory effect Effects 0.000 claims 2
- 201000006417 multiple sclerosis Diseases 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 239000001301 oxygen Substances 0.000 claims 2
- 230000036262 stenosis Effects 0.000 claims 2
- 208000037804 stenosis Diseases 0.000 claims 2
- RHFLHCFOTKICHL-YHQLXQCYSA-N (2r)-2-[(2s)-5,5-dimethylpyrrolidin-2-yl]-1-[4-[(5r,7s)-7-fluoro-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]-2-[2-fluoro-4-(trifluoromethyl)phenyl]ethanone Chemical compound C([C@H]1[C@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@@H](F)C[C@H](C=23)C)C=2C(=CC(=CC=2)C(F)(F)F)F)CC(C)(C)N1 RHFLHCFOTKICHL-YHQLXQCYSA-N 0.000 claims 1
- GGXGZWAQHASGSZ-JJXUHFIVSA-N (2s)-1-[4-[(5r)-7,7-difluoro-5-methyl-5,6-dihydrocyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]-2-[(2s)-5,5-dimethylpyrrolidin-2-yl]-2-[2-fluoro-4-(trifluoromethyl)phenyl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3C(F)(F)C[C@H](C=23)C)C=2C(=CC(=CC=2)C(F)(F)F)F)CC(C)(C)N1 GGXGZWAQHASGSZ-JJXUHFIVSA-N 0.000 claims 1
- DASSZTKFRRUZCP-DKOYFPBOSA-N (2s)-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]-2-[(2s)-1-methylpyrrolidin-2-yl]-2-(4-methylsulfonylphenyl)ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@H](O)C[C@H](C=23)C)C=2C=CC(=CC=2)S(C)(=O)=O)CCN1C DASSZTKFRRUZCP-DKOYFPBOSA-N 0.000 claims 1
- XFHVYPRSEDNUFU-QEMXTEJRSA-N (2s)-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]-2-[(2s)-1-methylpyrrolidin-2-yl]-2-[4-(trifluoromethyl)phenyl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@H](O)C[C@H](C=23)C)C=2C=CC(=CC=2)C(F)(F)F)CCN1C XFHVYPRSEDNUFU-QEMXTEJRSA-N 0.000 claims 1
- FEMSWPPUYTTWKZ-LKRGOLFISA-N (2s)-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]-2-[(2s)-pyrrolidin-2-yl]-2-[4-(trifluoromethyl)phenyl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@H](O)C[C@H](C=23)C)C=2C=CC(=CC=2)C(F)(F)F)CCN1 FEMSWPPUYTTWKZ-LKRGOLFISA-N 0.000 claims 1
- RNDKLFPVTJZXMV-DKOYFPBOSA-N (2s)-1-[4-[(5r,7r)-7-methoxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]-2-[(2s)-1-methylpyrrolidin-2-yl]-2-[4-(trifluoromethyl)phenyl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C2=NC=NC3=C2[C@H](C)C[C@H]3OC)C=2C=CC(=CC=2)C(F)(F)F)CCN1C RNDKLFPVTJZXMV-DKOYFPBOSA-N 0.000 claims 1
- GEERFIKIHAKETR-BTIFBSDPSA-N (2s)-2-(3,4-difluorophenyl)-2-[(2s)-5,5-dimethylpyrrolidin-2-yl]-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@H](O)C[C@H](C=23)C)C=2C=C(F)C(F)=CC=2)CC(C)(C)N1 GEERFIKIHAKETR-BTIFBSDPSA-N 0.000 claims 1
- NSQJPOIAYSLFDI-FHZYATBESA-N (2s)-2-(3-bromophenyl)-2-[(2s)-5,5-dimethylpyrrolidin-2-yl]-1-[4-[(5r)-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3CC[C@H](C=23)C)C=2C=C(Br)C=CC=2)CC(C)(C)N1 NSQJPOIAYSLFDI-FHZYATBESA-N 0.000 claims 1
- SIITXINKIRZLQU-QEMXTEJRSA-N (2s)-2-(3-bromophenyl)-2-[(2s)-5,5-dimethylpyrrolidin-2-yl]-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@H](O)C[C@H](C=23)C)C=2C=C(Br)C=CC=2)CC(C)(C)N1 SIITXINKIRZLQU-QEMXTEJRSA-N 0.000 claims 1
- BGOWNUNGLJHGKO-FHZYATBESA-N (2s)-2-(3-chlorophenyl)-2-[(2s)-5,5-dimethylpyrrolidin-2-yl]-1-[4-[(5r)-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3CC[C@H](C=23)C)C=2C=C(Cl)C=CC=2)CC(C)(C)N1 BGOWNUNGLJHGKO-FHZYATBESA-N 0.000 claims 1
- PKFWHNKIXDWAHF-QEMXTEJRSA-N (2s)-2-(3-chlorophenyl)-2-[(2s)-5,5-dimethylpyrrolidin-2-yl]-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@H](O)C[C@H](C=23)C)C=2C=C(Cl)C=CC=2)CC(C)(C)N1 PKFWHNKIXDWAHF-QEMXTEJRSA-N 0.000 claims 1
- YHTSWIVQYCSQER-BTIFBSDPSA-N (2s)-2-(4-bromo-2-fluorophenyl)-2-[(2s)-5,5-dimethylpyrrolidin-2-yl]-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@H](O)C[C@H](C=23)C)C=2C(=CC(Br)=CC=2)F)CC(C)(C)N1 YHTSWIVQYCSQER-BTIFBSDPSA-N 0.000 claims 1
- DMMDFDUBQHEPDQ-BTIFBSDPSA-N (2s)-2-(4-bromo-3-fluorophenyl)-2-[(2s)-5,5-dimethylpyrrolidin-2-yl]-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@H](O)C[C@H](C=23)C)C=2C=C(F)C(Br)=CC=2)CC(C)(C)N1 DMMDFDUBQHEPDQ-BTIFBSDPSA-N 0.000 claims 1
- ZGVMQUGMOPZOJC-PBEJRMEISA-N (2s)-2-(4-bromophenyl)-1-[4-[(5r)-7,7-difluoro-5-methyl-5,6-dihydrocyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]-2-[(2s)-5,5-dimethylpyrrolidin-2-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3C(F)(F)C[C@H](C=23)C)C=2C=CC(Br)=CC=2)CC(C)(C)N1 ZGVMQUGMOPZOJC-PBEJRMEISA-N 0.000 claims 1
- KOQKCNFHTUUWJI-DEZRYOJYSA-N (2s)-2-(4-bromophenyl)-2-[(2s)-5,5-dimethylpyrrolidin-2-yl]-1-[4-[(5r,7r)-7-fluoro-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@H](F)C[C@H](C=23)C)C=2C=CC(Br)=CC=2)CC(C)(C)N1 KOQKCNFHTUUWJI-DEZRYOJYSA-N 0.000 claims 1
- MCDVPXUUDXCZPQ-QEMXTEJRSA-N (2s)-2-(4-bromophenyl)-2-[(2s)-5,5-dimethylpyrrolidin-2-yl]-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@H](O)C[C@H](C=23)C)C=2C=CC(Br)=CC=2)CC(C)(C)N1 MCDVPXUUDXCZPQ-QEMXTEJRSA-N 0.000 claims 1
- MCDVPXUUDXCZPQ-SYNNKVJXSA-N (2s)-2-(4-bromophenyl)-2-[(2s)-5,5-dimethylpyrrolidin-2-yl]-1-[4-[(5r,7s)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@@H](O)C[C@H](C=23)C)C=2C=CC(Br)=CC=2)CC(C)(C)N1 MCDVPXUUDXCZPQ-SYNNKVJXSA-N 0.000 claims 1
- GGAYRRSQBOODLT-LDQFHDLZSA-N (2s)-2-(4-chloro-2,5-difluorophenyl)-2-[(2s)-5,5-dimethylpyrrolidin-2-yl]-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@H](O)C[C@H](C=23)C)C=2C(=CC(Cl)=C(F)C=2)F)CC(C)(C)N1 GGAYRRSQBOODLT-LDQFHDLZSA-N 0.000 claims 1
- OCYQNUNFTYVQRE-SURYNDKFSA-N (2s)-2-(4-chloro-2-fluorophenyl)-2-[(2s)-5,5-dimethylpyrrolidin-2-yl]-1-[4-[(5r,7r)-7-hydroxy-5,7-dimethyl-5,6-dihydrocyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@](C)(O)C[C@H](C=23)C)C=2C(=CC(Cl)=CC=2)F)CC(C)(C)N1 OCYQNUNFTYVQRE-SURYNDKFSA-N 0.000 claims 1
- ZBUKELXFBDMFKY-BTIFBSDPSA-N (2s)-2-(4-chloro-2-fluorophenyl)-2-[(2s)-5,5-dimethylpyrrolidin-2-yl]-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@H](O)C[C@H](C=23)C)C=2C(=CC(Cl)=CC=2)F)CC(C)(C)N1 ZBUKELXFBDMFKY-BTIFBSDPSA-N 0.000 claims 1
- AANZSBNNRYHRRN-BZDYGPBWSA-N (2s)-2-(4-chloro-2-fluorophenyl)-2-[(2s)-5,5-dimethylpyrrolidin-2-yl]-1-[4-[(5r,7s)-7-fluoro-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@@H](F)C[C@H](C=23)C)C=2C(=CC(Cl)=CC=2)F)CC(C)(C)N1 AANZSBNNRYHRRN-BZDYGPBWSA-N 0.000 claims 1
- YEKYBFOXPKLPFD-SURYNDKFSA-N (2s)-2-(4-chloro-3-fluorophenyl)-2-[(2s)-5,5-dimethylpyrrolidin-2-yl]-1-[4-[(5r,7r)-7-hydroxy-5,7-dimethyl-5,6-dihydrocyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@](C)(O)C[C@H](C=23)C)C=2C=C(F)C(Cl)=CC=2)CC(C)(C)N1 YEKYBFOXPKLPFD-SURYNDKFSA-N 0.000 claims 1
- DBNPCFRCZQQNNM-BZDYGPBWSA-N (2s)-2-(4-chloro-3-fluorophenyl)-2-[(2s)-5,5-dimethylpyrrolidin-2-yl]-1-[4-[(5r,7s)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@@H](O)C[C@H](C=23)C)C=2C=C(F)C(Cl)=CC=2)CC(C)(C)N1 DBNPCFRCZQQNNM-BZDYGPBWSA-N 0.000 claims 1
- OZZBPRLCCCVZBE-ZNPMGDIFSA-N (2s)-2-(4-chlorophenyl)-1-[(3s)-4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]-3-methylpiperazin-1-yl]-2-[(2s)-pyrrolidin-2-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN([C@H](C2)C)C=2N=CN=C3[C@H](O)C[C@H](C=23)C)C=2C=CC(Cl)=CC=2)CCN1 OZZBPRLCCCVZBE-ZNPMGDIFSA-N 0.000 claims 1
- KNIAUQMPYFBCJK-PBEJRMEISA-N (2s)-2-(4-chlorophenyl)-1-[4-[(5r)-7,7-difluoro-5-methyl-5,6-dihydrocyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]-2-[(2s)-5,5-dimethylpyrrolidin-2-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3C(F)(F)C[C@H](C=23)C)C=2C=CC(Cl)=CC=2)CC(C)(C)N1 KNIAUQMPYFBCJK-PBEJRMEISA-N 0.000 claims 1
- ZVYGXDZKUJTOIX-ZXFPDNNPSA-N (2s)-2-(4-chlorophenyl)-1-[4-[(5r,7r)-7-fluoro-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]-2-[(2s)-pyrrolidin-2-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@H](F)C[C@H](C=23)C)C=2C=CC(Cl)=CC=2)CCN1 ZVYGXDZKUJTOIX-ZXFPDNNPSA-N 0.000 claims 1
- PZDFWZSALKFSMT-ZEFBCVDJSA-N (2s)-2-(4-chlorophenyl)-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]-2-[(2r)-1-methylpyrrolidin-2-yl]ethanone Chemical compound C([C@@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@H](O)C[C@H](C=23)C)C=2C=CC(Cl)=CC=2)CCN1C PZDFWZSALKFSMT-ZEFBCVDJSA-N 0.000 claims 1
- NEEIYKGPXDSGBL-FEGHXTNJSA-N (2s)-2-(4-chlorophenyl)-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]-2-[(2r)-pyrrolidin-2-yl]ethanone Chemical compound C([C@@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@H](O)C[C@H](C=23)C)C=2C=CC(Cl)=CC=2)CCN1 NEEIYKGPXDSGBL-FEGHXTNJSA-N 0.000 claims 1
- GNMUHTCTEVMICV-DKOYFPBOSA-N (2s)-2-(4-chlorophenyl)-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]-2-[(2s)-1,5,5-trimethylpyrrolidin-2-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@H](O)C[C@H](C=23)C)C=2C=CC(Cl)=CC=2)CC(C)(C)N1C GNMUHTCTEVMICV-DKOYFPBOSA-N 0.000 claims 1
- ZOAWIPAEUPZJIV-QBTGUUFSSA-N (2s)-2-(4-chlorophenyl)-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]-2-[(2s)-1-(2-hydroxy-2-methylpropyl)pyrrolidin-2-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@H](O)C[C@H](C=23)C)C=2C=CC(Cl)=CC=2)CCN1CC(C)(C)O ZOAWIPAEUPZJIV-QBTGUUFSSA-N 0.000 claims 1
- PCTZNUMCLFOXCU-SRPRTCBCSA-N (2s)-2-(4-chlorophenyl)-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]-2-[(2s)-1-(2-methoxyethyl)-5,5-dimethylpyrrolidin-2-yl]ethanone Chemical compound C1CC(C)(C)N(CCOC)[C@@H]1[C@H](C=1C=CC(Cl)=CC=1)C(=O)N1CCN(C=2C=3[C@H](C)C[C@@H](O)C=3N=CN=2)CC1 PCTZNUMCLFOXCU-SRPRTCBCSA-N 0.000 claims 1
- SYVAKCTZZGZWME-QBTGUUFSSA-N (2s)-2-(4-chlorophenyl)-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]-2-[(2s)-1-(2-methoxyethyl)pyrrolidin-2-yl]ethanone Chemical compound COCCN1CCC[C@H]1[C@H](C=1C=CC(Cl)=CC=1)C(=O)N1CCN(C=2C=3[C@H](C)C[C@@H](O)C=3N=CN=2)CC1 SYVAKCTZZGZWME-QBTGUUFSSA-N 0.000 claims 1
- WZMPDSCDRPTBPT-SRPRTCBCSA-N (2s)-2-(4-chlorophenyl)-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]-2-[(2s)-1-(2-methylpropyl)pyrrolidin-2-yl]ethanone Chemical compound CC(C)CN1CCC[C@H]1[C@H](C=1C=CC(Cl)=CC=1)C(=O)N1CCN(C=2C=3[C@H](C)C[C@@H](O)C=3N=CN=2)CC1 WZMPDSCDRPTBPT-SRPRTCBCSA-N 0.000 claims 1
- GGDGKPLGOYLEOE-QBTGUUFSSA-N (2s)-2-(4-chlorophenyl)-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]-2-[(2s)-1-(3-hydroxypropyl)pyrrolidin-2-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@H](O)C[C@H](C=23)C)C=2C=CC(Cl)=CC=2)CCN1CCCO GGDGKPLGOYLEOE-QBTGUUFSSA-N 0.000 claims 1
- XCXDOUGVTGFDMW-XVZHEKKHSA-N (2s)-2-(4-chlorophenyl)-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]-2-[(2s)-1-(oxan-4-yl)pyrrolidin-2-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@H](O)C[C@H](C=23)C)C=2C=CC(Cl)=CC=2)CCN1C1CCOCC1 XCXDOUGVTGFDMW-XVZHEKKHSA-N 0.000 claims 1
- YHSDAHWHJFHOGJ-DKOYFPBOSA-N (2s)-2-(4-chlorophenyl)-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]-2-[(2s)-1-methylpiperidin-2-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@H](O)C[C@H](C=23)C)C=2C=CC(Cl)=CC=2)CCCN1C YHSDAHWHJFHOGJ-DKOYFPBOSA-N 0.000 claims 1
- BLBOCVKCGYAKDP-QBTGUUFSSA-N (2s)-2-(4-chlorophenyl)-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]-2-[(2s)-1-propan-2-ylpyrrolidin-2-yl]ethanone Chemical compound CC(C)N1CCC[C@H]1[C@H](C=1C=CC(Cl)=CC=1)C(=O)N1CCN(C=2C=3[C@H](C)C[C@@H](O)C=3N=CN=2)CC1 BLBOCVKCGYAKDP-QBTGUUFSSA-N 0.000 claims 1
- XLELDVURKKAFNR-QEMXTEJRSA-N (2s)-2-(4-chlorophenyl)-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]-2-[(2s)-piperidin-2-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@H](O)C[C@H](C=23)C)C=2C=CC(Cl)=CC=2)CCCN1 XLELDVURKKAFNR-QEMXTEJRSA-N 0.000 claims 1
- NEEIYKGPXDSGBL-LKRGOLFISA-N (2s)-2-(4-chlorophenyl)-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]-2-[(2s)-pyrrolidin-2-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@H](O)C[C@H](C=23)C)C=2C=CC(Cl)=CC=2)CCN1 NEEIYKGPXDSGBL-LKRGOLFISA-N 0.000 claims 1
- QLPNCJOLECYJKL-QEMXTEJRSA-N (2s)-2-(4-chlorophenyl)-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]-2-[(3r)-4-methylmorpholin-3-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@H](O)C[C@H](C=23)C)C=2C=CC(Cl)=CC=2)OCCN1C QLPNCJOLECYJKL-QEMXTEJRSA-N 0.000 claims 1
- PTVFSXRIKOGGFI-LKRGOLFISA-N (2s)-2-(4-chlorophenyl)-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]-2-[(3r)-morpholin-3-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@H](O)C[C@H](C=23)C)C=2C=CC(Cl)=CC=2)OCCN1 PTVFSXRIKOGGFI-LKRGOLFISA-N 0.000 claims 1
- ZVYGXDZKUJTOIX-CCMRYFRJSA-N (2s)-2-(4-chlorophenyl)-1-[4-[(5r,7s)-7-fluoro-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]-2-[(2s)-pyrrolidin-2-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@@H](F)C[C@H](C=23)C)C=2C=CC(Cl)=CC=2)CCN1 ZVYGXDZKUJTOIX-CCMRYFRJSA-N 0.000 claims 1
- PZDFWZSALKFSMT-SYNNKVJXSA-N (2s)-2-(4-chlorophenyl)-1-[4-[(5r,7s)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]-2-[(2s)-1-methylpyrrolidin-2-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@@H](O)C[C@H](C=23)C)C=2C=CC(Cl)=CC=2)CCN1C PZDFWZSALKFSMT-SYNNKVJXSA-N 0.000 claims 1
- NEEIYKGPXDSGBL-CCMRYFRJSA-N (2s)-2-(4-chlorophenyl)-1-[4-[(5r,7s)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]-2-[(2s)-pyrrolidin-2-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@@H](O)C[C@H](C=23)C)C=2C=CC(Cl)=CC=2)CCN1 NEEIYKGPXDSGBL-CCMRYFRJSA-N 0.000 claims 1
- QLPNCJOLECYJKL-SYNNKVJXSA-N (2s)-2-(4-chlorophenyl)-1-[4-[(5r,7s)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]-2-[(3r)-4-methylmorpholin-3-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@@H](O)C[C@H](C=23)C)C=2C=CC(Cl)=CC=2)OCCN1C QLPNCJOLECYJKL-SYNNKVJXSA-N 0.000 claims 1
- PTVFSXRIKOGGFI-CCMRYFRJSA-N (2s)-2-(4-chlorophenyl)-1-[4-[(5r,7s)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]-2-[(3r)-morpholin-3-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@@H](O)C[C@H](C=23)C)C=2C=CC(Cl)=CC=2)OCCN1 PTVFSXRIKOGGFI-CCMRYFRJSA-N 0.000 claims 1
- AMNJOBCQNPPENC-WOSKWAQLSA-N (2s)-2-(4-chlorophenyl)-2-[(2s)-1-(2,2-difluoroethyl)pyrrolidin-2-yl]-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@H](O)C[C@H](C=23)C)C=2C=CC(Cl)=CC=2)CCN1CC(F)F AMNJOBCQNPPENC-WOSKWAQLSA-N 0.000 claims 1
- DOYYJLRNVHHMGU-DKOYFPBOSA-N (2s)-2-(4-chlorophenyl)-2-[(2s)-1-(2-fluoroethyl)pyrrolidin-2-yl]-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@H](O)C[C@H](C=23)C)C=2C=CC(Cl)=CC=2)CCN1CCF DOYYJLRNVHHMGU-DKOYFPBOSA-N 0.000 claims 1
- DTWAQJRESWWCQZ-DKOYFPBOSA-N (2s)-2-(4-chlorophenyl)-2-[(2s)-1-(2-hydroxyethyl)pyrrolidin-2-yl]-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@H](O)C[C@H](C=23)C)C=2C=CC(Cl)=CC=2)CCN1CCO DTWAQJRESWWCQZ-DKOYFPBOSA-N 0.000 claims 1
- OJKNLOFSNGKISA-QBTGUUFSSA-N (2s)-2-(4-chlorophenyl)-2-[(2s)-1-ethyl-5,5-dimethylpyrrolidin-2-yl]-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]ethanone Chemical compound C1CC(C)(C)N(CC)[C@@H]1[C@H](C=1C=CC(Cl)=CC=1)C(=O)N1CCN(C=2C=3[C@H](C)C[C@@H](O)C=3N=CN=2)CC1 OJKNLOFSNGKISA-QBTGUUFSSA-N 0.000 claims 1
- OJKNLOFSNGKISA-VPJOFFEXSA-N (2s)-2-(4-chlorophenyl)-2-[(2s)-1-ethyl-5,5-dimethylpyrrolidin-2-yl]-1-[4-[(5r,7s)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]ethanone Chemical compound C1CC(C)(C)N(CC)[C@@H]1[C@H](C=1C=CC(Cl)=CC=1)C(=O)N1CCN(C=2C=3[C@H](C)C[C@H](O)C=3N=CN=2)CC1 OJKNLOFSNGKISA-VPJOFFEXSA-N 0.000 claims 1
- SGYPPIWCNUQKNU-QBTGUUFSSA-N (2s)-2-(4-chlorophenyl)-2-[(2s)-5,5-diethylpyrrolidin-2-yl]-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]ethanone Chemical compound N1C(CC)(CC)CC[C@H]1[C@H](C=1C=CC(Cl)=CC=1)C(=O)N1CCN(C=2C=3[C@H](C)C[C@@H](O)C=3N=CN=2)CC1 SGYPPIWCNUQKNU-QBTGUUFSSA-N 0.000 claims 1
- AATFGCSBGPLZTP-WJMWBRGCSA-N (2s)-2-(4-chlorophenyl)-2-[(2s)-5,5-dimethylpyrrolidin-2-yl]-1-[4-[(5r,7r)-5-(fluoromethyl)-7-hydroxy-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]ethanone Chemical compound N1C(C)(C)CC[C@H]1[C@H](C=1C=CC(Cl)=CC=1)C(=O)N1CCN(C=2C=3[C@H](CF)C[C@@H](O)C=3N=CN=2)CC1 AATFGCSBGPLZTP-WJMWBRGCSA-N 0.000 claims 1
- ASVATSKHMUOZCG-WCSGGZKSSA-N (2s)-2-(4-chlorophenyl)-2-[(2s)-5,5-dimethylpyrrolidin-2-yl]-1-[4-[(5r,7r)-7-hydroxy-5,7-dimethyl-5,6-dihydrocyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@](C)(O)C[C@H](C=23)C)C=2C=CC(Cl)=CC=2)CC(C)(C)N1 ASVATSKHMUOZCG-WCSGGZKSSA-N 0.000 claims 1
- JFTIFYNZZKGWRZ-WJMWBRGCSA-N (2s)-2-(4-chlorophenyl)-2-[(2s)-5,5-dimethylpyrrolidin-2-yl]-1-[4-[(5r,7r)-7-hydroxy-5-(hydroxymethyl)-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]ethanone Chemical compound N1C(C)(C)CC[C@H]1[C@H](C=1C=CC(Cl)=CC=1)C(=O)N1CCN(C=2C=3[C@H](CO)C[C@@H](O)C=3N=CN=2)CC1 JFTIFYNZZKGWRZ-WJMWBRGCSA-N 0.000 claims 1
- KOHGXVITISGBPV-QEMXTEJRSA-N (2s)-2-(4-chlorophenyl)-2-[(2s)-5,5-dimethylpyrrolidin-2-yl]-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@H](O)C[C@H](C=23)C)C=2C=CC(Cl)=CC=2)CC(C)(C)N1 KOHGXVITISGBPV-QEMXTEJRSA-N 0.000 claims 1
- AXICWQITLRXKEH-DKOYFPBOSA-N (2s)-2-(4-chlorophenyl)-2-[(2s)-5,5-dimethylpyrrolidin-2-yl]-1-[4-[(5r,7r)-7-methoxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C2=NC=NC3=C2[C@H](C)C[C@H]3OC)C=2C=CC(Cl)=CC=2)CC(C)(C)N1 AXICWQITLRXKEH-DKOYFPBOSA-N 0.000 claims 1
- KOHGXVITISGBPV-SYNNKVJXSA-N (2s)-2-(4-chlorophenyl)-2-[(2s)-5,5-dimethylpyrrolidin-2-yl]-1-[4-[(5r,7s)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@@H](O)C[C@H](C=23)C)C=2C=CC(Cl)=CC=2)CC(C)(C)N1 KOHGXVITISGBPV-SYNNKVJXSA-N 0.000 claims 1
- LWAIVXYLRFXPLQ-ZJNJKDKRSA-N (2s)-2-(4-cyclopropylphenyl)-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]-2-[(2s)-1-methylpyrrolidin-2-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@H](O)C[C@H](C=23)C)C=2C=CC(=CC=2)C2CC2)CCN1C LWAIVXYLRFXPLQ-ZJNJKDKRSA-N 0.000 claims 1
- GMSADNDLRCPPJI-TVZVLCPFSA-N (2s)-2-(4-cyclopropylphenyl)-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]-2-[(2s)-1-propan-2-ylpyrrolidin-2-yl]ethanone Chemical compound CC(C)N1CCC[C@H]1[C@H](C=1C=CC(=CC=1)C1CC1)C(=O)N1CCN(C=2C=3[C@H](C)C[C@@H](O)C=3N=CN=2)CC1 GMSADNDLRCPPJI-TVZVLCPFSA-N 0.000 claims 1
- DNNUTZJOWDKFAP-TYVKFHQSSA-N (2s)-2-(4-cyclopropylphenyl)-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]-2-[(2s)-pyrrolidin-2-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@H](O)C[C@H](C=23)C)C=2C=CC(=CC=2)C2CC2)CCN1 DNNUTZJOWDKFAP-TYVKFHQSSA-N 0.000 claims 1
- BJLNTTHYSROJML-XVZHEKKHSA-N (2s)-2-(4-cyclopropylphenyl)-2-[(2s)-1-ethylpyrrolidin-2-yl]-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]ethanone Chemical compound CCN1CCC[C@H]1[C@H](C=1C=CC(=CC=1)C1CC1)C(=O)N1CCN(C=2C=3[C@H](C)C[C@@H](O)C=3N=CN=2)CC1 BJLNTTHYSROJML-XVZHEKKHSA-N 0.000 claims 1
- JUPHFKZPZRICTE-ZJNJKDKRSA-N (2s)-2-(4-cyclopropylphenyl)-2-[(2s)-5,5-dimethylpyrrolidin-2-yl]-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@H](O)C[C@H](C=23)C)C=2C=CC(=CC=2)C2CC2)CC(C)(C)N1 JUPHFKZPZRICTE-ZJNJKDKRSA-N 0.000 claims 1
- JUPHFKZPZRICTE-SPTRTZJMSA-N (2s)-2-(4-cyclopropylphenyl)-2-[(2s)-5,5-dimethylpyrrolidin-2-yl]-1-[4-[(5r,7s)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@@H](O)C[C@H](C=23)C)C=2C=CC(=CC=2)C2CC2)CC(C)(C)N1 JUPHFKZPZRICTE-SPTRTZJMSA-N 0.000 claims 1
- POXBGKDKQNKAPI-SRPRTCBCSA-N (2s)-2-(4-tert-butylphenyl)-2-[(2s)-5,5-dimethylpyrrolidin-2-yl]-1-[4-[(5r,7r)-7-hydroxy-5-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-4-yl]piperazin-1-yl]ethanone Chemical compound C([C@H]1[C@@H](C(=O)N2CCN(CC2)C=2N=CN=C3[C@H](O)C[C@H](C=23)C)C=2C=CC(=CC=2)C(C)(C)C)CC(C)(C)N1 POXBGKDKQNKAPI-SRPRTCBCSA-N 0.000 claims 1
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Abstract
ciclopentanos de pirimidil como inibidores de akt proteína cinase a presente invenção fornece compostos de fórmula 1, incluindo tautômeros, enantiômeros resolvidos, diastereômeros, solvatos, metabólitos, sais e pró-fármacos farmaceuticamente aceitáveis dos mesmos também são fornecidos métodos de emprego dos compostos desta invenção como inibidores de akt proteína cinase e para o tratamento de doenças hiperproliferativas tais como câncer
Description
Relatório Descritivo da Patente de Invenção para CICLOPENTANOS DE PIRIMIDIL, PROCESSO DE PREPARAÇÃO DOS MESMOS, COMPOSIÇÃO FARMACÊUTICA QUE OS COMPREENDE, KIT E USO. ANTECEDENTES DA INVENÇÃO
Prioridade de Invenção
Este pedido reivindica prioridade para o Pedido Provisional dos Estados Unidos Número 60/948.138 que foi depositado em 5 de julho de 2007, e Pedido Provisional dos Estados Unidos Número 61/020.088 que foi depositado em 9 de janeiro de 2008, ambos os quais estão por meio deste incorporados aqui por referência em sua totalidade.
Campo da Invenção
Esta invenção refere-se ao novos inibidores de serina/treonina proteína cinases (por exemplo, AKT e cinases relacionadas), composições farmacêuticas que contêm os inibidores, e métodos para a preparação destes inibidores. Os inibidores, são úteis, por exemplo, para o tratamento de doenças hiperproliferativas, tais como câncer e inflamação, em mamíferos. Descrição do Estado da Técnica
Proteína cinases (PK) são enzimas que catalisam a fosforilação de grupos hidróxi em resíduos de tirosina, serina e treonina de proteínas por transferência do (gama) fosfato terminal de ATP. Por meio de séries de reações de transdução de sinal, estas enzimas modulam crescimento, diferenciação e proliferação celular, isto é, virtualmente todos aspectos da vida celular de uma maneira ou de outra dependem da atividade de PK (Hardie, G. e Hanks, S. (1995) The Protein Kinase Facts Books I and II, Academic Press, San Diego, CA). Além disso, atividade de PK anormal foi relacionada com um hospedeiro de distúrbios, variando de doenças que relativamente não ameaçam a vida tais como psoríase a doenças extremamente virulentas tais como glioblastoma (câncer cerebral). Proteína cinases são uma classe-alvo importante para a modulação terapêutica (Cohen, P. (2002) Nature Rev. Drug Discovery 1:309).
Significantemente, a fosforilação e/ou expressão de proteína atípica é frequentemente relatada como sendo um dos efeitos causadores de proliferação celular anormal, metástase e sobrevivência celular em cân-
Claims (15)
1. Composto, caracterizado pelo fato de que apresenta a Fórmula:
R2 R2a e enantiômeros e sais do mesmo, em que:
G é fenila, naftaleno, uma heteroarila de 5 a 6 membros ou uma heteroarila bicíclica de 9 a 10 membros em que a fenila, naftaleno, heteroarila de 5 a 6 membros ou heteroarila bicíclica de 9 a 10 membros é opcionalmente substituído com um a quatro grupos Ra;
R1 e R1a são independentemente selecionados de H, Me, Et, CH=CH2, -CH2OH, CF3, CHF2 ou CH2F;
R2 é H, -OH, -OMe ou F;
R2a é H, Me ou F, ou
R2 e R2a são oxo;
R3 é H, Me, Et, ou CF3;
R4 é H, heterociclo de 4 a 6 membros, ciclopropilmetila ou C1-C4 alquila opcionalmente substituída com F, -OH ou -O(Ci-C3 alquila);
R5 e R5a são independentemente selecionados de H e C-1-C4 alquila, ou R5 e R5a juntamente com o átomo ao qual eles estão ligados formam um grupo carbonila, uma cicloalquila de 5 a 6 membros ou um heterociclo de 5 a 6 membros, em que o heterociclo tem um heteroátomo de oxigênio;
cada Ra é independentemente halogênio, Ci-C6-alquila, C3-C6cicloalquila, -O-ÍCrCe-alquila), CF3, -OCF3, S^-Ce-alquila), CN, fenila, 2
OCH2-fenila, NH2, -NO2, -NH-(Ci-C6-alquila), -N-(C1-C6-alquila)2, piperidina, pirrolidina, pirazol, piridina, 2-aminopiridina, CH2F, CHF2, -OCH2F, -OCHF2, OH, -SO2(Ci-C6-alquila), C(O)NH2, C(O)NH(Ci-C6-alquila), e CfOMCrCealquila)2; e j é 1 ou 2; e quando j for 2, o NR4 oposto ao carbono no anel j pode ser substituído com um heteroátomo de O.
2-il)etanona;
(S)-2-(4-clorofenil)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((R)-pirrolidin-2-il)etanona;
(S)-2-(4-clorofenil)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7R)-5(fluorometil)-7-hidróxi-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1il)etanona;
(S)-2-(4-clorofenil)-1-(4-((R)-7,7-difluoro-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((S)-5,5-dimetilpirrolidin-2il)etanona;
(S)-2-(4-cloro-3-fluorofenil)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((R)-pirrolidin-2-il)etanona;
(S)-2-(4-clorofenil)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((R)-1-metilpirrolidin-2-il)etanona;
(S)-2-(4-clorofenil)-2-((S)-1-(2,2-difluoroetil)pirrolidin-2-il)-1-(4-((5R,7R)-7hidróxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1il)etanona;
(S)-2-(4-clorofenil)-2-((S)-1-(2-fluoroetil)pirrolidin-2-il)-1-(4-((5R,7R)-7-hidróxi5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)etanona;
(S)-2-(5-clorotiofen-2-il)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((S)-pirrolidin-2-il)etanona;
(S)-2-(5-clorotiofen-2-il)-1-(4-((5R,7S)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((S)-pirrolidin-2-il)etanona; (S)-2-(4-clorofenil)-1-((S)-4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)-3-metilpiperazin-1-il)-2-((S)-pirrolidin-2-il)etanona; (S)-1-(4-((5R,7R)-7-hidróxi-5,7-dimetil-6,7-dihidro-5H-ciclopenta[d]pirimidin-
2. Composto, caracterizado pelo fato de que apresenta a Fórmula:
e enantiômeros e sais do mesmo, em que:
G é fenila opcionalmente substituída com um a quatro grupos Ra ou uma heteroarila de 5 a 6 membros opcionalmente substituída por um halogênio;
R1 e R1a são independentemente selecionados de H, Me, Et, CH=CH2, -CH2OH, CF3, CHF2 ou CH2F;
R2 é H, -OH, -OMe ou F;
R2a é H, Me ou F, ou
R2 e R2a são oxo;
R3 é H, Me, Et, ou CF3;
R4 é H, heterociclo de 4 a 6 membros, ciclopropilmetila ou C1-C4 alquila opcionalmente substituída com F, -OH ou -O(Ci-C3 alquila);
R5 e R5a são independentemente selecionados de H e C-i-C4 alquila, ou R5 e R5a juntamente com o átomo ao qual eles estão ligados formam uma cicloalquila de 5 a 6 membros ou heterociclo de 5 a 6 membros, em que o heterociclo tem um heteroátomo de oxigênio;
cada Ra é independentemente halogênio, Ci-Ce-alquila, C3-C6cicloalquila, -O-(Ci-C6-alquila), CF3, -OCF3, SÍCrCe-alquila), CN, -OCH2fenila, NH2, -NO2, -NH-(CrC6-alquila), -N-(Ci-C6-alquila)2, piperidina, pirrolidina, CH2F, CHF2, -OCH2F, -OCHF2i -OH, -SO^CrCe-alquila), C(O)NH2, C(O)NH(Ci-C6-alquila), e C(O)N(Ci-C6-alquila)2;
j é 1 ou 2; e quando j for 2, o NR4 oposto ao carbono no anel j pode ser substituído com um heteroátomo de O.
3-fluorofenila, 2-fluoro-4-metoxifenila, 4-(1 H-pirazol-4-il)fenila, bifenil-4-ila, 4(2-aminopirimidin-5-il)fenila, 4-terc-butilfenila, 2,3-difluoro-4(trifluorometil)fenila, 2-fluoro-3-(trifluorometil)fenila, 2-fluoro-5(trifluorometil)fenila, 4-(trifluorometóxi)fenila, e 3-fluoro-4- (trifl uorometóxi)fen ila.
45. Composto de acordo com a reivindicação 2, caracterizado pelo fato de ser mencionado nos Exemplos 1 a 32.
46. Composto de acordo com a reivindicação 2, caracterizado pelo fato de ser mencionado nos Exemplos 1 a 100.
47. Composto, caracterizado pelo fato de que é selecionado dentre: (S)-2-(4-clorofenil)-1-(4-((5R,7R)-7-fluoro-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((S)-pirrolidin-2-il)etanona; (S)-2-(4-clorofenil)-1-(4-((5R,7S)-7-fluoro-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((S)-pirrolidin-2-il)etanona; (S)-2-(4-clorofenil)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((S)-pirrolidin-2-il)etanona;
(S)-2-(4-clorofenil)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((S)-piperidin-2-il)etanona;
(S)-2-(3-fluoro-4-(trifluorometil)fenil)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((S)-pirrolidin-2il)etanona;
(S)-2-(4-clorofenil)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((S)-1-metilpiperidin-2-il)etanona;
(S)-2-(4-clorofenil)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihrdro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((S)-1-metilpirrolidin-2-il)etanona; (S)-2-(4-clorofenil)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((S)-1-isopropilpirrolidin-2il)etanona;
(S)-2-(4-clorofenil)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((S)-1-isobutilpirrolidin-2il)etanona;
(S)-2-(4-clorofenil)-1-(4-((5R,7S)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((S)-1-metilpirrolidin-2-il)etanona;
(S)-2-(4-clorofenil)-1-(4-((5R,7S)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((S)-pirrolidin-2-il)etanona;
(S)-2-(4-clorofenil)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1 -il)-2-((S)-1,5,5-trimetilpirrolidin-2il)etanona;
(S)-2-(4-ciclopropilfenil)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((S)-pirrolidin-2-il)etanona; (S)-2-(4-clorofenil)-2-((S)-1-etilpirrolidin-2-il)-1-(4-((5R,7R)-7-hidróxi-5-metil-
3. Composto de acordo com a reivindicação 2, caracterizado pelo fato de que
R2 é selecionado de H, -OH, -OMe ou F;
R2a é selecionado de H, Me ou F;
R4 é H, heterociclo de 4 a 6 membros, ciclopropilmetila ou C1-C4 alquila opcionalmente substituída com -OH ou -O(Ci-C3 alquila);
R5 e R5a são independentemente selecionados de H e C1-C4 alquila; e j é 1 ou 2.
4-((S)-1-((S)-5,5-dimetilpirrolidin-2-il)-2-(4-((5R,7R)-7-hidróxi-5-metil-6,7dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-oxoetil)-2 fluorobenzonitrile;
(S)-2-(4-clorofenil)-1-(4-((5R,7S)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((R)-morfolin-3-il)etanona; (S)-2-(4-clorofenil)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((R)-4-metilmorfolin-3-il)etanona;
(S)-2-(4-clorofenil)-1-(4-((5R,7S)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((R)-4-metilmorfolin-3-il)etanona;
(S)-2-(4-clorofenil)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((R)-morfolin-3-il)etanona;
(S)-2-(4-cloro-2,5-difluorofenil)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7R)7-hidróxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1il)etanona;
(S)-2-(4-cloro-2-fluorofenil)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7R)-7hidróxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1il)etanona;
(S)-2-(4-bromo-2-fluorofenil)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7R)-7hidróxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1il)etanona;
(S)-2-(4-bromo-3-fluorofenil)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7R)-7hidróxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1il)etanona;
(S)-2-(3-clorofenil)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7R)-7-hidróxi-5metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)etanona;
(S)-1-(4-((5R,7R)-7-metóxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4il)piperazin-1-il)-2-((S)-pirrolidin-2-il)-2-(4-(trifluorometil)fenil)etanona;
(S)-2-(4-cloro-2-fluorofenil)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7R)-7hidróxi-5,7-dimetil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1il)etanona;
(S)-2-(4-cloro-2-fluorofenil)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7S)-7fluoro-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)etanona;
(S)-2-((S)-5,5-dimetilpirrolidin-2-il)-2-(2-fluoro-4-metilfenil)-1-(4-((5R,7R)-7hidróxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-116 il)etanona;
(S)-2-(2,4-diclorofenil)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7R)-7-hidróxi-
4-((S)-2-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4il)piperazin-1-il)-1-((S)-1-metilpirrolidin-2-il)-2-oxoetil)benzamide;
(S)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7R)-7-hidróxi-5,7-dimetil-6,7dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-(4(trifluorometil)fenil)etanona;
(S)-2-((S)-5,5-dimetilpirrolidin-2-il)-2-(3-fluoro-4-(trifluorometil)fenil)-1-(4((5R,7R)-7-hidróxi-5,7-dimetil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4il)piperazin-1 -il)etanona;
(S)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4il)piperazin-1-il)-2-(4-(metilsulfonil)fenil)-2-((S)-pirrolidin-2-il)etanona;
(S)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4il)piperazin-1-il)-2-((S)-1-metilpirrolidin-2-il)-2-(4-(metilsulfonil)fenil)etanona; (S)-2-(4-cloro-3-fluorofenil)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7R)-7hidróxi-5,7-dimetil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1il)etanona;
(S)-2-(4-bromofenil)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7R)-7-hidróxi-
4-((S)-2-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4il)piperazin-1-il)-2-oxo-1-((S)-pirrolidin-2-il)etil)benzamide;
4-((S)-2-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4il)piperazin-1-il)-1-((S)-1-metilpirrolidin-2-il)-2-oxoetil)benzonitrile;
(S)-2-(4-clorofenil)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7R)-7-hidróxi-5,7dimetil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)etanona;
(S)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-(4-(trifluorometil)fenil)etanona;
(S)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7S)-7-hidróxi-5-metil-6,7-dihidro5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-(4-(trifluorometil)fenil)etanona;
(S)-2-(4-bromofenil)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7R)-7-hidróxi-5metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)etanona;
(S)-2-(4-bromofenil)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7S)-7-hidróxi-5metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)etanona;
(S)-2-((S)-5,5-dimetilpirrolidin-2-il)-2-(2-fluoro-4-(trifluorometil)fenil)-1-(4((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin1-il)etanona;
(S)-2-((S)-5,5-dimetilpirrolidin-2-il)-2-(2-fluoro-4-(trifluorometil)fenil)-1-(4((5R,7S)-7-hidróxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin1-il)etanona;
(S)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7R)-7-fluoro-5-metil-6,7-dihidro5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-(4-(trifluorometil)fenil)etanona; (S)-2-(4-bromofenil)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7R)-7-fluoro-5metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)etanona;
(S)-1-(4-((5R,7R)-7-metóxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4il)piperazin-1-il)-2-((S)-pirrolidin-2-il)-2-(4-(trifluorometil)fenil)etanona; (S)-2-(4-clorofenil)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7R)-7-metóxi-5metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)etanona;
(S)-2-(4-clorofenil)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7R)-7-hidróxi-5(hidróximetil)-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)etanona; (S)-2-(4-bromofenil)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7S)-7-fluoro-5metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)etanona;
(S)-2-(4-bromofenil)-1-(4-((R)-7,7-difluoro-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1 -il)-2-((S)-5,5-dimetilpirrolidin-2il)etanona;
(S)-1-(4-((R)-7,7-difluoro-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4il)piperazin-1 -il)-2-((S)-5,5-dimetilpirrolidin-2-il)-2-(2-fluoro-4(trifluorometil)fenil)etanona;
(R)-1-(4-((R)-7,7-difluoro-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4il)piperazin-1-rl)-2-((S)-5,5-dimetilpirrolidin-2-il)-2-(4(trifluorometil)fenil)etanona;
(R)-2-((S)-5,5-dimetilpirrolidin-2-il)-2-(2-fluoro-4-(trifluorometil)fenil)-1-(4((5R,7S)-7-fluoro-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin1-il)etanona;
(S)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7S)-7-fluoro-5-metil-6,7-dihidro5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-(4-(trifluorometil)fenil)etanona; 4-((S)-1-((S)-5,5-dimetilpirrolidin-2-il)-2-(4-((5R,7R)-7-hidróxi-5-metil-6,7dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-oxoetil)benzonitrile;
(S)-2-(4-clorofenil)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((R)-5-(hidróximetil)-
4-((S)-2-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4il)piperazin-1-il)-2-oxo-1-((S)-pirrolidin-2-il)etil)benzonitrile;
4-il)piperazin-1-il)-2-((S)-pirrolidin-2-il)-2-(4-(trifluorometil)fenil)etanona;
(S)-2-(5-clorotiofen-2-il)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((S)-1-metilpirrolidin-2-il)etanona;
(S)-2-(5-clorotiofen-2-il)-1-(4-((5R,7S)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((S)-1-metilpirrolidin-2-il)etanona;
(S)-2-(3-fluoro-4-(trifluorometil)fenil)-1-(4-((5R,7S)-7-hidróxi-5-metil-6,7dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((S)-pirrolidin-2il)etanona;
(S)-2-(5-bromotiofen-2-il)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((S)-pirrolidin-2-il)etanona;
(S)-2-(5-bromotiofen-2-il)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((S)-1-metilpirrolidin-2-il)etanona; (S)-1-(4-((5R,7R)-7-hidróxi-5,7-dimetil-6,7-dihidro-5H-ciclopenta[d]pirimidin4-il)piperazin-1-il)-2-((S)-1-metilpirrolidin-2-il)-2-(4(trifluorometil)fenil)etanona;
4. Composto de acordo com qualquer uma das reivindicações 1 a 3, caracterizado pelo fato de que R3 é H.
5 reivindicação 1 ou 2, caracterizado pelo fato de que compreende:
(a) reação de um composto da fórmula 8:
ou um sal do mesmo, com um composto da fórmula 83:
R5 (Á_ÚR5a / J \ v^boc
G y
OH para preparar um composto de fórmula 84:
(b) desproteção do composto de fórmula 84; e
5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)etanona;
(S)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-(naftalen-2-il)etanona;
(S)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((R)-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-(naftalen-2-il)etanona; (S)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-(naftalen-1-il)etanona;
(S)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((R)-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-(naftalen-1-il)etanona;
(S)-2-(3,4-diclorofenil)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7R)-7-hidróxi5-metil-6,7-dihidro-5H-ciclopenta[d]pirinnidin-4-il)piperazin-1-il)etanona;
(S)-2-(3,4-difluorofenil)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7R)-7hidróxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1il)etanona;
(S)-2-((S)-5,5-dimetilpirrolidin-2-il)-2-(4-fluorofenil)-1-(4-((5R,7R)-7-hidróxi-5metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)etanona;
(S)-2-((S)-5,5-dimetilpirrolidin-2-il)-2-(4-fluoro-3-(trifluorometil)fenil)-1-(4((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin1-il)etanona;
(S)-2-(3-clorofenil)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((R)-5-metil-6,7dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)etanona;
(S)-2-(3-bromofenil)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7R)-7-hidróxi-5metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)etanona;
(S)-2-(3-bromofenil)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((R)-5-metil-6,7dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)etanona;
(S)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-(3-(trifluorometil)fenil)etanona;
(S)-2-((S)-5,5-dimetilpirrolidin-2-il)-2-(3-fluorofenil)-1-(4-((5R,7R)-7-hidróxi-5metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)etanona;
(S)-2-((S)-5,5-dimetilpirrolidin-2-il)-2-(2-fluoro-4-metóxifenil)-1-(4-((5R,7R)-7 hidróxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1il)etanona;
(S)-2-(4-(1H-pirazol-4-il)fenil)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7R)-7hidróxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1il)etanona;
(S)-2-(bifenil-4-il)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7R)-7-hidróxi-5metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)etanona;
(S)-2-(4-(2-aminopirimidin-5-il)fenil)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin1-il)etanona;
(S)-2-(4-tert-butilfenil)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7R)-7-hidróxi5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)etanona; (S)-2-(2,3-difluoro-4-(trifluorometil)fenil)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin1-il)etanona;
(S)-2-((S)-5,5-dimetilpirrolidin-2-il)-2-(2-fluoro-3-(trifluorometil)fenil)-1-(4((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin1-il)etanona;
(S)-2-((S)-5,5-dimetilpirrolidin-2-il)-2-(2-fluoro-5-(trifluorometil)fenil)-1-(4((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin1-il)etanona;
(S)-5-((S)-2-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-oxo-1-(4(trifluorometil)fenil)etil)pirrolidin-2-ona;
(R)-5-((S)-2-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1 -il)-2-oxo-1 -(4(trifluorometil)fenil)etil)pirrolidin-2-ona;
(R) -5-((S)-1-(4-clorofenil)-2-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-oxoetil)pirrolidin-2-ona;
(S) -5-((S)-1-(4-clorofenil)-2-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-oxoetil)pirrolidin-2-ona;
(S)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro
5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-(4(trifluorometóxi)fenil)etanona;
(S)-2-((S)-5,5-dimetilpirrolidin-2-il)-2-(3-fluoro-4-(trifluorometóxi)fenil)-1-(4((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin1-il)etanona;
(S)-2-(5-bromotiofen-2-il)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7R)-7hidróxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1il)etanona;
(S)-2-(5-clorotiofen-2-il)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7R)-7hidróxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1il)etanona; and (S)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-(1H-indol-3-il)etanona;
e sais dos mesmos.
48. Composição farmacêutica, caracterizada pelo fato de que compreende um composto como definido em qualquer uma das reivindicações 1 a 47.
49. Método de tratamento de uma doença ou distúrbio mediado por AKT em um mamífero, caracterizado pelo fato de que compreende administrar ao referido mamífero uma quantidade eficaz de um composto como definido em qualquer uma das reivindicações 1 a 47.
50. Método de acordo com a reivindicação 49, caracterizado pelo fato de que a referida doença ou distúrbio é doença inflamatória, hiperproliferativa, cardiovascular, neurodegenerativa, ginecológica, ou dermatológica.
51. Método de inibição da produção de AKT proteína cinase em um mamífero, caracterizado pelo fato de que compreende administrar ao referido mamífero uma quantidade eficaz de um composto como definido em qualquer uma das reivindicações 1 a 47.
52. Composto de acordo com qualquer uma das reivindicações 1 a 47, caracterizado pelo fato de ser para uso como medicamento no tratamento de condições mediadas por AKT proteína cinase.
53. Uso de um composto, como definido em qualquer uma das reivindicações 1 a 47, caracterizado pelo fato de ser na produção de um medicamento para o tratamento de condições mediadas por AKT proteína cinase ou para inibição da produção de AKT proteína cinase.
54. Kit para o tratamento de uma condição mediada por AKT proteína cinase, caracterizado pelo fato de que compreende:
a) uma primeira composição farmacêutica compreendendo um composto como definido em qualquer uma das reivindicações 1 a 47; e
b) instruções para uso.
55. Kit de acordo com a reivindicação 54, caracterizado pelo fato de que compreende ainda (c) uma segunda composição farmacêutica, em que a segunda composição farmacêutica compreende um segundo composto que é um inibidor de AKT proteína cinase.
56. Processo de preparação de um composto, como definido na reivindicação 1 ou 2, caracterizado pelo fato de que compreende:
(a) reação de um composto da fórmula 8:
ou um sal do mesmo, com um composto da fórmula 7: R5
OH
para preparar um composto de fórmula 9:
Rl o
N
R2 R2a (b) desproteção do composto de fórmula 9; e (c) opcionalmente funcionalização do composto de fórmula 9 para preparar um composto de fórmula I.
57. Processo de preparação de um composto, como definido na
5,7-dimetil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)etanona;
5. Composto de acordo com qualquer uma das reivindicações 1 a 4, caracterizado pelo fato de que R5 é H.
6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)etanona;
(S)-1-(4-((5R,7R)-7-metóxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4il)piperazin-1-il)-2-((S)-1-metilpirrolidin-2-il)-2-(4-(trifluorometil)fenil)etanona;
(S)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4il)piperazin-1-il)-2-((S)-pirrolidin-2-il)-2-(4-(trifluorometil)fenil)etanona; (S)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4il)piperazin-1-il)-2-((S)-1-metilpirrolidin-2-il)-2-(4-(trifluorometil)fenil)etanona;
(S)-2-(4-ciclopropilfenil)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7R)-7hidróxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1il)etanona;
(S)-2-(4-ciclopropilfenil)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7S)-7hidróxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1il)etanona;
(R) -4-(4-((S)-2-(4-clorofenil)-2-((S)-5,5-dimetilpirrolidin-2-il)acetil)piperazin-1il)-5-metil-5H-ciclopenta[d]pirimidin-7(6H)-ona;
(S) -2-(4-clorofenil)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7S)-7-fluoro-5metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)etanona; (S)-2-(4-cloro-3-fluorofenil)-1-(4-((5R,7S)-7-fluoro-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((S)-pirrolidin-2-il)etanona;
(S)-2-((S)-5,5-dimetilpirrolidin-2-il)-2-(3-fluoro-4-(trifluorometil)fenil)-1-(4((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin1-il)etanona;
(S)-2-((S)-5,5-dimetilpirrolidin-2-il)-2-(3-fluoro-4-(trifluorometil)fenil)-1-(4((5R,7S)-7-hidróxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin1-il)etanona;
(S)-2-(4-cloro-3-fluorofenil)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7R)-7hidróxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-114 il)etanona;
(S)-2-(4-cloro-3-fluorofenil)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7S)-7hidróxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1il)etanona;
(S)-2-(4-clorofenil)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((S)-1-azaspiro[4.4]nonan-2il)etanona;
(S)-2-(4-clorofenil)-2-((S)-5,5-dietilpirrolidin-2-il)-1-(4-((5R,7R)-7-hidróxi-5metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)etanona; (S)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-(4-(metilsulfonil)fenil)etanona;
6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)etanona;
(S)-2-(4-clorofenil)-2-((S)-1-(ciclopropilmetil)pirrolrdin-2-il)-1-(4-((5R,7R)-7hidróxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1il)etanona;
(S)-2-(4-clorofenil)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((S)-1-(tetrahidro-2H-piran-4il)pirrolidin-2-il)etanona;
(S)-2-(4-clorofenil)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((S)-1-(2-hidróxietil)pirrolidin-2il)etanona;
(S)-2-(4-clorofenil)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7R)-7-hidróxi-5metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)etanona;
(S)-2-(4-clorofenil)-2-((S)-1-(2-hidróxi-2-metilpropil)pirrolidin-2-il)-1-(4((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin1-il)etanona;
(S)-2-(4-clorofenil)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((S)-1-(3-hidróxipropil)pirrolidin-2il)etanona;
(S)-2-(4-ciclopropilfenil)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((S)-1-metilpirrolidin-2-il)etanona;
(S)-2-(4-ciclopropilfenil)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((S)-1-isopropilpirrolidin-2il)etanona;
(S)-2-(4-clorofenil)-2-((S)-1-etil-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7R)-7hidróxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1il)etanona;
(S)-2-(4-clorofenil)-2-((S)-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7S)-7-hidróxi-5metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)etanona;
(S)-2-(4-clorofenil)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((S)-1-(2-metóxietil)-5,5dimetilpirrolidin-2-il)etanona;
(S)-2-(4-clorofenil)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((S)-1-(2-metóxietil)pirrolidin-2il)etanona;
(S)-2-(4-cloro-3-fluorofenil)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((S)-1-metilpirrolidin-2-il)etanona;
(S)-2-(4-cloro-3-fluorofenil)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((S)-pirrolidin-2-il)etanona;
(S)-2-(4-cloro-3-fluorofenil)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5H10 ciclopenta[d]pirimidin-4-il)piperazin-1 -il)-2-((S)-1-isopropilpirrolidin-2il)etanona (S)-2-(4-clorofenil)-1-(4-((5R,7S)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((S)-1,5,5-trimetilpirrolidin-2il)etanona;
(S)-2-(4-clorofenil)-2-((S)-1-etil-5,5-dimetilpirrolidin-2-il)-1-(4-((5R,7S)-7hidróxi-5-metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1il)etanona;
(S)-2-(4-ciclopropilfenil)-2-((S)-1-etilpirrolidin-2-il)-1-(4-((5R,7R)-7-hidróxi-5metil-6,7-dihidro-5H-ciclopenta[d]pirimidin-4-il)piperazin-1-il)etanona;
(S)-2-(4-clorofenil)-1-(4-((5R,7R)-7-hidróxi-5-metil-6,7-dihidro-5Hciclopenta[d]pirimidin-4-il)piperazin-1-il)-2-((S)-1-(2,2,2-trifluoroetil)pirrolidin-
6. Composto de acordo com qualquer uma das reivindicações 1 a 5, caracterizado pelo fato de que R5a é H.
7. Composto de acordo com qualquer uma das reivindicações 1 a 4, caracterizado pelo fato de que R5 é metila.
8. Composto de acordo com qualquer uma das reivindicações 1 a 5 e 7, caracterizado pelo fato de que R5a é metila.
9. Composto de acordo com qualquer uma das reivindicações 1 a 4, caracterizado pelo fato de que R5 é etila.
10 (c) opcionalmente funcionalização do composto de fórmula 84 para preparar um composto de fórmula I.
58. Composto de acordo com a reivindicação 52 ou uso de acordo com a reivindicação 53, caracterizado pelo fato de que a condição mediada por AKT proteína cinase é selecionada dentre artrite reumatoide, osteo artrite, doença de Crohn, angiofibroma, doenças oculares, esclerose múltipla, obesidade, re-estenose, doenças autoimunes, alergia, asma, endometriose, aterosclerose, estenose de enxerto de veia, estenose de enxerto profético perianastomático, hiperplasia da próstata, doença pulmonar obstrutiva crônica, psoríase, inibição de dano neurológico devido à reparação de tecido, formação de tecido de cicatriz, esclerose múltipla, doença inflamatória do intestino, infecções, doença pulmonar, neoplasma, doença de Parkinson, rejeição de transplante e choque séptico.
59. Composto de acordo com a reivindicação 52 ou uso de acordo com a reivindicação 53, caracterizado pelo fato de que a condição mediada por AKT proteína cinase é uma doença hiperproliferativa.
60. Composto de acordo com a reivindicação 52 ou uso de acordo com a reivindicação 53, caracterizado pelo fato de que a condição mediada por AKT proteína cinase é um câncer.
61. Composto ou uso de acordo com a reivindicação 59, caracterizado pelo fato de que o câncer é selecionado dentre cardíaco, pulmão, gastrointestinal, trato genitourinário, fígado, ósseo, sistema nervoso, ginecológico, hematológico, pele, glândula suprarrenal, mama, cólon, cavidade oral, leucemia de células pilosas, cabeça e pescoço, doença metastática refratária, sarcoma de Kaposi, síndrome de Bannayan-Zonana, doença de Cowden e doença de Lhermitte-Duclos.
62. Composto de acordo com qualquer uma das reivindicações 1 a 47 e um fármaco farmaceuticamente ativo adicional, caracterizado pelo fato de ser para uso como medicamentos no tratamento de condições mediadas por AKT proteína cinase.
63. Composto de acordo com a reivindicação 62, caracterizado pelo fato de que o fármaco farmaceuticamente ativo adicional é um agente quimioterapêutico.
64. Composto de acordo com a reivindicação 62, caracterizado pelo fato de que o composto ou o sal do mesmo e o fármaco farmaceuticamente ativo adicional são administrados juntos em uma composição farmacêutica unitária.
65. Composto de acordo com a reivindicação 62, caracterizado pelo fato de que o composto ou o sal do mesmo e o fármaco farmaceuticamente ativo adicional são administrados separadamente e são administrados simultaneamente ou sequencialmente.
5
66. Composto de acordo com a reivindicação 62, caracterizado pelo fato de que o fármaco farmaceuticamente ativo adicional é selecionado dentre erlotinib, trastuzumab, bevacizumab, rituximab, bortezomib, fulvestranto, sutent, letrozol, mesilato de imatinib, PTK787/ZK 222584, oxaliplatina, 5-fluoracil, leucovorina, rapamicina, lapatinib, lonafarnib, sorafenib, gefitinib, 10 AG1478, AG1571, tiotepa, ciclosfosfamida, doxorrubicina, paclitaxel e doxetaxel.
67. Composto de acordo com a reivindicação 62, caracterizado pelo fato de que o fármaco farmaceuticamente ativo adicional é um agente de alquilação.
10. Composto de acordo com qualquer uma das reivindicações 1 a 5, 7 e 9, caracterizado pelo fato de que R5a é etila.
11. Composto de acordo com qualquer uma das reivindicações 1 a 4, caracterizado pelo fato de que R5 e R5a juntamente com o átomo ao qual eles estão ligados formam uma cicloalquila de 5 a 6 membros.
12. Composto de acordo com a reivindicação 11, caracterizado pelo fato de que R5 e R5a juntamente com o átomo ao qual eles estão ligados formam uma cicloalquila de 5 a 6 membros, tendo a estrutura:
em que k é 1 ou 2 e a linha ondulada está onde a estrutura liga-se à piperazina requerida de fórmula I.
13. Composto de acordo com qualquer uma das reivindicações 1 a 4, caracterizado pelo fato de que R5 e R5a juntamente com o átomo ao qual eles estão ligados formam um heterociclo de 5 a 6 membros, em que o heterociclo tem um heteroátomo de oxigênio.
14. Composto de acordo com a reivindicação 13, caracterizado pelo fato de que R5 e R5a juntamente com o átomo ao qual eles estão ligados formam um heterociclo de 5 a 6 membros, em que o heterociclo tem um heteroátomo de oxigênio, tendo a estrutura:
em que k é 1 ou 2 e a linha ondulada está onde a estrutura liga-se à piperazina requerida de fórmula I.
15. Composto de acordo com qualquer uma das reivindicações 1 a 14, caracterizado pelo fato de que R1 é metila.
16. Composto de acordo com qualquer uma das reivindicações 1 a 15, caracterizado pelo fato de que R1 é metila opcionalmente na configura ção (R).
17. Composto de acordo com qualquer uma das reivindicações 1 a 16, caracterizado pelo fato de que R1a é H.
18. Composto de acordo com qualquer uma das reivindicações 1 a 16, caracterizado pelo fato de que R1a é metila.
19. Composto de acordo com qualquer uma das reivindicações 1 a 14, caracterizado pelo fato de que R1 é H.
20. Composto de acordo com qualquer uma das reivindicações 1 a 14, caracterizado pelo fato de que R1 é etila.
21. Composto de acordo com qualquer uma das reivindicações 1 a 14, caracterizado pelo fato de que R1 é CH=CH2.
22. Composto de acordo com qualquer uma das reivindicações 1 a 14, caracterizado pelo fato de que R1 é CH2OH.
23. Composto de acordo com qualquer uma das reivindicações 1 a 14, caracterizado pelo fato de que R1 é CH2F.
24. Composto de acordo com qualquer uma das reivindicações 1 a 14 e 18 a 23, caracterizado pelo fato de que R1a é H.
25. Composto de acordo com qualquer uma das reivindicações 1 a 24, caracterizado pelo fato de que R2a é H.
26. Composto de acordo com qualquer uma das reivindicações 1 a 25, caracterizado pelo fato de que R2 é F.
27. Composto de acordo com qualquer uma das reivindicações 1 a 25, caracterizado pelo fato de que R2 é OH.
28. Composto de acordo com qualquer uma das reivindicações 1 a 24, caracterizado pelo fato de que R2 é F.
29. Composto de acordo com qualquer uma das reivindicações 1 a 24 e 28, caracterizado pelo fato de que R2a é F.
30. Composto de acordo com qualquer uma das reivindicações 1 a 25, caracterizado pelo fato de que R2 é -OMe.
31. Composto de acordo com qualquer uma das reivindicações 1 a 13, caracterizado pelo fato de que G é selecionado de 4-clorofenila, 3fluoro-4-clorofenila, 3-fluoro-4-trifluorometilfenila e 4-ciclopropilfenila.
32. Composto de acordo com qualquer uma das reivindicações 1 a 30, caracterizado pelo fato de que G é selecionado de 4-clorofenila, 4bromofenila, 4-ciclopropilfenila, 4-trifluorometilfenila, 4-cianofenila, 4benzamida, 4-(metilsulfonil)fenila, 2-fluoro-4-trifluorometilfenila, 3-fluoro-4clorofenila ,3-fluoro-4-trifluorometilfenila ou 3-fluoro-4-cianofenila.
33. Composto de acordo com qualquer uma das reivindicações 1 a 32, caracterizado pelo fato de que R4 é C1-C4 alquila opcionalmente substituída com OH ou O(CrC3 alquila).
34. Composto de acordo com qualquer uma das reivindicações 1 a 33, caracterizado pelo fato de que R4 é selecionado de metila, etila, isopropila, isobutila, CH2CH2OH, CH2CH2CH2OH, CH2C(CH3)2OH e CH2CH2OCH3.
35. Composto de acordo com qualquer uma das reivindicações 1 a 33, caracterizado pelo fato de que R4 é ciclopropilmetila.
36. Composto de acordo com qualquer uma das reivindicações 1 a 33, caracterizado pelo fato de que R4 é um heterociclo de 4 a 6 membros.
37. Composto de acordo com qualquer uma das reivindicações 1 a 33 e 36, caracterizado pelo fato de que R4 é tetra-hidropiranila.
38. Composto de acordo com qualquer uma das reivindicações 1 a 32, caracterizado pelo fato de que R4 é H.
39. Composto de acordo com qualquer uma das reivindicações 1 a 32, caracterizado pelo fato de que R4 é C1-C4 alquila opcionalmente substituída com F.
40. Composto de acordo com a reivindicação 39, caracterizado pelo fato de que R4 é CH2CF3, CH2CH2F ou CH2CHF2.
41. Composto de acordo com qualquer uma das reivindicações 1 a 40, caracterizado pelo fato de que j é 1.
42. Composto de acordo com qualquer uma das reivindicações 1 a 40, caracterizado pelo fato de que j é 2.
43. Composto de acordo com qualquer uma das reivindicações 1 a 4, caracterizado pelo fato de que R5 e R5a juntamente com o átomo ao qual eles estão ligados formam um grupo oxo, tendo a estrutura:
em que a linha ondulada está onde a estrutura liga-se à piperazina requerida de fórmula I.
44. Composto de acordo com qualquer uma das reivindicações 1 a 30, caracterizado pelo fato de que G é 4-clorofenila, 4-bromofenila, 4ciclopropilfenila, 4-trifluorometilfenila, 4-cianofenila, 4-benzamida, 4(metilsulfonil)fenila, 2-fluoro-4-trifluorometilfenila, 3-fluoro-4-clorofenila, 3fluoro-4-trifluorometilfenila, 3-fluoro-4-cianofenila, 4-cloro-2,5-difluorofenila, 4-cloro-2-fluorofenila, 4-bromo-2-fluorofenila, 4-bromo-3-fluorofenila, 3clorofenila, 2-fluoro-4-metilfenila, 2,4-diclorofenila, 3,4-diclorofenila, 4fluorofenila, 4-fluoro-3-trifluorometilfenila, 3-bromofenila, 3-trifluorometilfenila,
15 68. Invenção, caracterizada por quaisquer de suas concretizações ou categorias de reivindicação englobadas pela matéria inicialmente revelada no pedido de patente ou em seus exemplos aqui apresentados.
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| PCT/US2008/069144 WO2009006567A2 (en) | 2007-07-05 | 2008-07-03 | Pyrimidyl cyclopentanes as akt protein kinase inhibitors |
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