HRP20140807T1 - Derivati pirolo[2,3-d]pirimidina kao inhibitori protein kinaze b - Google Patents
Derivati pirolo[2,3-d]pirimidina kao inhibitori protein kinaze b Download PDFInfo
- Publication number
- HRP20140807T1 HRP20140807T1 HRP20140807AT HRP20140807T HRP20140807T1 HR P20140807 T1 HRP20140807 T1 HR P20140807T1 HR P20140807A T HRP20140807A T HR P20140807AT HR P20140807 T HRP20140807 T HR P20140807T HR P20140807 T1 HRP20140807 T1 HR P20140807T1
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- cancer
- pharmaceutically acceptable
- acceptable salt
- compound according
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- 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
- C07D487/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/26—Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
- C07D473/32—Nitrogen atom
- C07D473/34—Nitrogen atom attached in position 6, e.g. adenine
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Oncology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Claims (19)
1. Spoj naznačen time da je: (S)-4-amino-N-(1-(4-klorofenil)-3-hidroksipropil)-1-(7H-pirolo[2,3-d]pirimidin-4-il)piperidin-4-karboksamid:
[image]
ili njegova farmaceutski prihvatljiva sol.
2. Farmaceutski pripravak naznačen time da sadrži spoj prema zahtjevu 1, ili njegovu farmaceutski prihvatljivu sol, zajedno s farmaceutski prihvatljivim razrjeđivačem ili nosačem.
3. Spoj prema zahtjevu 1, ili njegova farmaceutski prihvatljiva sol, naznačen time da je za uporabu kao lijek.
4. Spoj prema zahtjevu 1, ili njegova farmaceutski prihvatljiva sol, naznačen time da je za uporabu za liječenje raka.
5. Spoj prema zahtjevu 1, ili njegova farmaceutski prihvatljiva sol, naznačen time da je za uporabu za liječenje raka, gdje je rak odabran od raka dojke, ne-Hodgkinovog limfoma, raka gušterače, hepatocelularnog karcinoma, raka želuca, raka prostate i raka pluća.
6. Spoj prema zahtjevu 1, ili njegova farmaceutski prihvatljiva sol, naznačen time da je za uporabu za liječenje raka dojke.
7. Uporaba spoja prema zahtjevu 1, ili njegove farmaceutski prihvatljive soli, naznačena time da je za pripravu lijeka za liječenje raka.
8. Uporaba spoja prema zahtjevu 1, ili njegove farmaceutski prihvatljive soli, naznačena time da je za pripravu lijeka za liječenje raka, gdje je rak odabran od raka dojke, ne-Hodgkinovog limfoma, raka gušterače, hepatocelularnog karcinoma, raka želuca, raka prostate i raka pluća.
9. Uporaba spoja prema zahtjevu 1, ili njegove farmaceutski prihvatljive soli, naznačena time da je za pripravu lijeka za liječenje raka dojke.
10. Spoj: (S)-4-amino-N-(1-(4-klorofenil)-3-hidroksipropil)-1-(7H-pirolo[2,3-d]pirimidin-4-il)piperidin-4-karboksamid, kako je zatraženo u zahtjevu 1.
11. Spoj prema zahtjevu 10 naznačen time da je za uporabu kod liječenja raka.
12. Spoj prema zahtjevu 10 naznačen time da je za uporabu kod liječenja raka gdje je rak odabran od raka dojke, ne-Hodgkinovog limfoma, raka gušterače, hepatocelularnog karcinoma, raka želuca, raka prostate i raka pluća.
13. Spoj prema zahtjevu 10 naznačen time da je za uporabu kod liječenja raka dojke.
14. Postupak za pripravu spoja prema zahtjevu 1, ili njegove farmaceutski prihvatljive soli, naznačen time da postupak sadrži reakciju kiseline Formule (II) i (S)-3-amino-3-(4-klorofenil)propan-1-ola:
[image]
pri čemu P1 predstavlja pogodnu zaštitnu skupinu; te nakon toga, ako je potrebno:
uklanjanje zaštitne skupine; i/ili
tvorbu njegove farmaceutski prihvatljive soli.
15. Postupak prema zahtjevu 14, naznačen time da P1 predstavlja tert-butoksikarbonil zaštitnu skupinu.
16. Spoj: (S)-tert-butil4-(1-(4-klorofenil)-3-hidroksipropilkarbamoil)-1-(7H-pirolo[2,3-d]pirimidin-4-il)piperidin-4-ilkarbamat:
[image]
17. Postupak za pripravu spoja prema zahtjevu 1, ili njegove farmaceutski prihvatljive soli, naznačen time da postupak sadrži reakciju (S)-4-amino-N-(1-(4-klorofenil)-3-hidroksipropil)piperidin-4-karboksamida sa bicikličkim heterociklom sa Formulom (V):
[image]
pri čemu L1 predstavlja pogodnu odlazeću skupinu; te nakon toga ako je potrebno, tvorbu njegove farmaceutski prihvatljive soli.
18. Postupak prema zahtjevu 17, naznačen time da L1 je klor.
19. Spoj: (S)-4-amino-N-(1-(4-klorofenil)-3-hidroksipropil)piperidin-4-karboksamid:
[image]
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US97919207P | 2007-10-11 | 2007-10-11 | |
| US4786208P | 2008-04-25 | 2008-04-25 | |
| PCT/GB2008/050925 WO2009047563A1 (en) | 2007-10-11 | 2008-10-09 | Pyrrolo [2, 3 -d] pyrimidin derivatives as protein kinase b inhibitors |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HRP20140807T1 true HRP20140807T1 (hr) | 2014-11-21 |
Family
ID=40251789
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HRP20140807AT HRP20140807T1 (hr) | 2007-10-11 | 2008-10-09 | Derivati pirolo[2,3-d]pirimidina kao inhibitori protein kinaze b |
Country Status (43)
Families Citing this family (45)
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