HRP20160655T1 - Supstituirani spojevi purina i 7-deazapurina kao modulatori epigenetskih enzima - Google Patents
Supstituirani spojevi purina i 7-deazapurina kao modulatori epigenetskih enzima Download PDFInfo
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- HRP20160655T1 HRP20160655T1 HRP20160655TT HRP20160655T HRP20160655T1 HR P20160655 T1 HRP20160655 T1 HR P20160655T1 HR P20160655T T HRP20160655T T HR P20160655TT HR P20160655 T HRP20160655 T HR P20160655T HR P20160655 T1 HRP20160655 T1 HR P20160655T1
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- 150000001875 compounds Chemical class 0.000 title claims 16
- 102000004190 Enzymes Human genes 0.000 title 1
- 108090000790 Enzymes Proteins 0.000 title 1
- KDCGOANMDULRCW-UHFFFAOYSA-N Purine Natural products N1=CNC2=NC=NC2=C1 KDCGOANMDULRCW-UHFFFAOYSA-N 0.000 title 1
- 230000001973 epigenetic effect Effects 0.000 title 1
- 125000000561 purinyl group Chemical class N1=C(N=C2N=CNC2=C1)* 0.000 title 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 19
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 19
- 125000005843 halogen group Chemical group 0.000 claims 18
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims 15
- 125000000041 C6-C10 aryl group Chemical group 0.000 claims 11
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 11
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 11
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 10
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 10
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 10
- 125000004093 cyano group Chemical group *C#N 0.000 claims 9
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims 8
- 125000001424 substituent group Chemical group 0.000 claims 8
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 6
- 208000032839 leukemia Diseases 0.000 claims 6
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 5
- 239000000825 pharmaceutical preparation Substances 0.000 claims 5
- -1 cyano, hydroxyl Chemical group 0.000 claims 4
- 125000001313 C5-C10 heteroaryl group Chemical group 0.000 claims 3
- 229910052703 rhodium Inorganic materials 0.000 claims 3
- 150000003839 salts Chemical class 0.000 claims 3
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims 2
- SWKAVEUTKGKHSR-UHFFFAOYSA-N 3-(benzylsulfamoyl)-4-bromo-n-(4-bromophenyl)benzamide Chemical compound C1=CC(Br)=CC=C1NC(=O)C1=CC=C(Br)C(S(=O)(=O)NCC=2C=CC=CC=2)=C1 SWKAVEUTKGKHSR-UHFFFAOYSA-N 0.000 claims 2
- 150000001204 N-oxides Chemical class 0.000 claims 2
- 206010028980 Neoplasm Diseases 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 125000003118 aryl group Chemical group 0.000 claims 2
- 201000011510 cancer Diseases 0.000 claims 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 2
- 208000024893 Acute lymphoblastic leukemia Diseases 0.000 claims 1
- 208000014697 Acute lymphocytic leukaemia Diseases 0.000 claims 1
- 208000031261 Acute myeloid leukaemia Diseases 0.000 claims 1
- 208000033776 Myeloid Acute Leukemia Diseases 0.000 claims 1
- 208000006664 Precursor Cell Lymphoblastic Leukemia-Lymphoma Diseases 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 230000002489 hematologic effect Effects 0.000 claims 1
- 125000001072 heteroaryl group Chemical group 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- 125000003566 oxetanyl group Chemical group 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 238000002560 therapeutic procedure Methods 0.000 claims 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
- 125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 0.000 claims 1
- GBXQPDCOMJJCMJ-UHFFFAOYSA-M trimethyl-[6-(trimethylazaniumyl)hexyl]azanium;bromide Chemical compound [Br-].C[N+](C)(C)CCCCCC[N+](C)(C)C GBXQPDCOMJJCMJ-UHFFFAOYSA-M 0.000 claims 1
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- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
- A61K31/52—Purines, e.g. adenine
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- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
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- A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
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- A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
- A61K31/7076—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines containing purines, e.g. adenosine, adenylic acid
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- A61P25/00—Drugs for disorders of the nervous system
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- C07D473/32—Nitrogen atom
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- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
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Claims (17)
1. Spoj s Formulom (IV) ili njegov N-oksid ili njegova farmaceutski prihvatljiva sol:
[image]
naznačen time da
A je O ili CH2;
Q je H, NH2, NHRb, NRbRc, OH, Rb, ili ORb, gdje svaki od Rb i Rc neovisno je C1-C6 alkil, C2-C6 alkenil, C2-C6 alkinil, C3-C8 cikloalkil, C6-C10 aril, 4 do 7-člani heterocikloalkil, 5 do 10-člani heteroaril, ili -M1-T1 gdje M1 je veza ili C1-C6 alkil poveznica proizvoljno supstituirana s halo, cijano, hidroksil ili C1-C6 alkoksil i T1 je C3-C8 cikloalkil, C6-C10 aril, 4 do 6-člani heterocikloalkil, ili 5 do 10-člani heteroaril, ili Rb i Rc, zajedno sa N atomom na koji su oni vezani, tvore 4 do 7-člani heterocikloalkil koji ima 0 ili 1 dodatnih heteroatoma na N atomu proizvoljno supstituiran s C1-C6 alkil, C2-C6 alkenil, C2-C6 alkinil, halo, hidroksil, karboksil, C(O)OH, C(O)O-C1-C6 alkil, OC(O)-C1-C6 alkil, cijano, C1-C6 alkoksil, amino, mono-C1-C6 alkilamino, di-C1-C6 alkilamino, C3-C8 cikloalkil, C6-C10 aril, 4 do 6-člani heterocikloalkil, ili 5 do 6-člani heteroaril, i svaki od Rb, Rc, i T1 je proizvoljno supstituiran s jednim ili više supstituenata odabranih iz skupine koja sadrži C1-C6 alkil, C2-C6 alkenil, C2-C6 alkinil, halo, hidroksil, karboksil, cijano, C1-C6 alkoksil, amino, mono-C1-C6 alkilamino, di-C1-C6 alkilamino, C3-C8 cikloalkil, C6-C10 aril, 4 do 6-člani heterocikloalkil, i 5 do 6-člani heteroaril;
X je N ili CRx, gdje Rx je H, halo, hidroksil, karboksil, cijano, ili RS1, RS1 je amino, C1-C6 alkoksil, C1-C6 alkil, C2-C6 alkenil, C2-C6 alkinil, C3-C8 cikloalkil, C6-C10 aril, 4 do 6-člani heterocikloalkil, ili 5 do 6-člani heteroaril, i RS1 je proizvoljno supstituiran s jednim ili više supstituenata odabranih iz skupine koja sadrži halo, hidroksil, karboksil, cijano, C1-C6 alkoksil, amino, mono-C1-C6 alkilamino, di-C1-C6 alkilamino, C3-C8 cikloalkil, C6-C10 aril, 4 do 6-člani heterocikloalkil, i 5 do 6-člani heteroaril;
Y je H, Rd, SO2Rd, ili CORd, Rd je C1-C6 alkil, C2-C6 alkenil, C2-C6 alkinil, C3-C8 cikloalkil, C6-C10 aril, 4 do 6-člani heterocikloalkil, ili 5 do 6-člani heteroaril, te Rd je proizvoljno supstituiran s jednim ili više supstituenata odabranih iz skupine koja sadrži C1-C6 alkil, C2-C6 alkenil, C2-C6 alkinil, halo, hidroksil, karboksil, cijano, C1-C6 alkoksil, C1-C6 alkilsulfonil, amino, mono-C1-C6 alkilamino, di-C1-C6 alkilamino, C3-C8 cikloalkil, C6-C10 aril, 4 do 6-člani heterocikloalkil, i 5 do 6-člani heteroaril i svaki od which C3-C8 cikloalkil, C6-C10 aril, 4 do 6-člani heterocikloalkil, i 5 do 6-člani heteroaril supstituenti na Rd je dodatno proizvoljno supstituiran s C1-C6 alkil, C2-C6 alkenil, C2-C6 alkinil, halo, hidroksil, karboksil, C(O)OH, C(O)O-C1-C6 alkil, OC(O)-C1-C6 alkil, cijano, C1-C6 alkoksil, amino, mono-C1-C6 alkilamino, di-C1-C6 alkilamino, C3-C8 cikloalkil, C6-C10 aril, 4 do 6-člani heterocikloalkil, ili 5 do 6-člani heteroaril;
svaki od R1 i R2 neovisno, je H, halo, hidroksil, karboksil, cijano, RS2, RS2 je amino, C1-C6 alkoksil, C1-C6 alkil, C2-C6 alkenil, ili C2-C6 alkinil, i svaki RS2 je proizvoljno supstituiran s jednim ili više supstituenata odabranih iz skupine koja sadrži halo, hidroksil, karboksil, cijano, C1-C6 alkoksil, amino, mono-C1-C6 alkilamino, di-C1-C6 alkilamino, C3-C8 cikloalkil, C6-C10 aril, 4 do 6-člani heterocikloalkil, i 5 do 6-člani heteroaril;
svaki od Re, Rf, Rg, i Rh, neovisno je -M2-T2, u kojem M2 je veza, SO2, SO, S, CO, CO2, O, O-C1-C4 alkil poveznica, C1-C4 alkil poveznica, NH, ili N(Rt), Rt je C1-C6 alkil, i T2 je H, halo, ili RS4, RS4 je C1-C6 alkil, C2-C6 alkenil, C2-C6 alkinil, C3-C8 cikloalkil, C6-C10 aril, 4 do 8-člani heterocikloalkil, ili 5 do 10-člani heteroaril, i svaki od O-C1-C4 alkil poveznice, C1-C4 alkil poveznice, Rt, i RS4 je proizvoljno supstituiran s jednim ili više supstituenata odabranih iz skupine koja sadrži halo, hidroksil, karboksil, cijano, C1-C6 alkil, C2-C6 alkenil, C2-C6 alkinil, C1-C6 alkoksil, amino, mono-C1-C6 alkilamino, di-C1-C6 alkilamino, C3-C8 cikloalkil, C6-C10 aril, 4 do 6-člani heterocikloalkil, i 5 do 6-člani heteroaril, i
m je 0, 1, ili 2.
2. Spoj prema zahtjevu 1, naznačen time da A je O.
3. Spoj prema zahtjevu 1, naznačen time da A je O i m je 2.
4. Spoj prema zahtjevu 1, naznačen time da X je N.
5. Spoj prema zahtjevu 1, naznačen time da Q je NH2 ili NHRb, gdje Rb je -M1-T1, M1 je veza ili C1-C6 alkil poveznica i T1 je C3-C8 cikloalkil.
6. Spoj prema zahtjevu 1, naznačen time da R1 i R2, su svaki H.
7. Spoj prema zahtjevu 1, naznačen time da Y je Rd.
8. Spoj prema zahtjevu 7, naznačen time da Rd je C1-C6 alkil proizvoljno supstituiran s C3-C8 cikloalkil ili halo, ili Rd je C3-C8 cikloalkil proizvoljno supstituiran s C1-C6 alkil ili halo.
9. Spoj prema zahtjevu 1, naznačen time da barem jedan od Re, Rf, Rg, i Rh je halo, C1-C6 alkoksil proizvoljno supstituiran s jednim ili više halo, C1-C6 alkilsulfonil proizvoljno supstituiran s jednim ili više halo, C1-C6 alkil proizvoljno supstituiran s jednim ili više supstituenata odabranih od halo, hidroksi, i C1-C6 alkoksil, C3-C8 cikloalkil proizvoljno supstituiran s jednim ili više C1-C6 alkil, ili 4 do 8-člani heterocikloalkil proizvoljno supstituiran s jednim ili više C1-C6 alkil.
10. Spoj prema zahtjevu 9, naznačen time da je barem jedan od Re, Rf, Rg, i Rh izabran iz skupine koju čine F, Cl, Br, CF3, OCF3, SO2CF3, oksetanil, C1-C4 alkoksil, C3-C8 cikloalkil proizvoljno supstituiran s jednim ili više supstituenata odabranih od C1-C4 alkil i CN, i C1-C4 alkil proizvoljno supstituiran s jednim ili više supstituenata odabranih od CN, halo, C3-C8 cikloalkil, hidroksi i C1-C6 alkoksil.
11. Spoj prema zahtjevu 1, naznačen time da je odabran iz skupa koji čine
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i N-oksidi i njihove farmaceutski prihvatljive soli.
12. Spoj prema zahtjevu 1, naznačen time da je spoj odabran od
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i njegovih farmaceutski prihvatljivih soli.
Farmaceutski pripravak naznačen time da sadrži terapijski učinkovitu količinu spoja prema bilo kojem od zahtjeva 1 do 12 i farmaceutski prihvatljiv nosač.
13. Spoj prema bilo kojem od patentnih zahtjeva 1 do 12 ili farmaceutski pripravak prema zahtjevu 13, naznačen time da je za upotrebu za terapiju.
14. Farmaceutski pripravak prema zahtjevu 13 naznačen time da je za upotrebu za liječenje raka.
15. Farmaceutski pripravak prema zahtjevu 13 naznačen time da je za upotrebu za liječenje hematološkog raka ili leukemije.
16. Farmaceutski pripravak za upotrebu prema zahtjevu 16, naznačen time da leukemija je akutna mijeloična leukemija, akutna limfocitna leukemija ili mješovita leukemija.
17. Farmaceutski pripravak za upotrebu prema zahtjevu 16, pri čemu leukemija je MLL-presložena leukemija ili leukemija naznačena time da ima parcijalnu tandem duplikaciju MLL gena (MLL-PTD).
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PCT/US2011/063044 WO2012075381A1 (en) | 2010-12-03 | 2011-12-02 | Substituted purine and 7 - deazapurine compounds as modulators of epigenetic enzymes |
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