ME02513B - Deuterizovani 1-piperazino-3-fenil indani za tretiranje šizofrenije - Google Patents
Deuterizovani 1-piperazino-3-fenil indani za tretiranje šizofrenijeInfo
- Publication number
- ME02513B ME02513B MEP-2016-226A MEP2016226A ME02513B ME 02513 B ME02513 B ME 02513B ME P2016226 A MEP2016226 A ME P2016226A ME 02513 B ME02513 B ME 02513B
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- ME
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- Prior art keywords
- compound
- deuterium
- atom
- labeled
- disorder
- Prior art date
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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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/451—Non condensed piperidines, e.g. piperocaine having a carbocyclic group directly attached to the heterocyclic ring, e.g. glutethimide, meperidine, loperamide, phencyclidine, piminodine
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
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- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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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
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- 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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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- A—HUMAN NECESSITIES
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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
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
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- A61K31/00—Medicinal preparations containing organic active ingredients
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/554—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one sulfur as ring hetero atoms, e.g. clothiapine, diltiazem
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- C07B59/002—Heterocyclic compounds
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- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
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- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
- C07C45/67—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
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- C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
- C07D241/04—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
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- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/06—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by halogen atoms or nitro radicals
- C07D295/073—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by halogen atoms or nitro radicals with the ring nitrogen atoms and the substituents separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
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Claims (31)
1.Jedinjenje formule Y: u kojoj,R1 - R10 su nezavisno vodonik ili deuterijum, pri čemu su R6-R10 svaki deuterijum, i gde najmanje jedan od R1-R10 obuhvata najmanje oko 50% deuterijuma, ili njegova farmaceutski prihvatljiva adiciona so sa kiselinom.
2. Jedinjenje prema zahtevu 1, u kojem su R3-R5 svaki vodonik.
3. Jedinjenje prema zahtevu 1, u kojem su R3-R5 svaki deuterijum.
4. Jedinjenje prema zahtevu 2, gde je jedinjenje
5. Jedinjenje prema zahtevu 2, gde je jedinjenje
6. Jedinjenje prema zahtevu 3, gde je jedinjenje
7. Jedinjenje prema zahtevu 3, gde je jedinjenje
8. Jedinjenje prema zahtevu 1, u kojem su R1 i R2 svaki deuterijum.
9. Jedinjenje prema zahtevu 8, u kojem su R3-R5 svaki deuterijum.
10. Jedinjenje prema zahtevu 8, u kojem su R3-R5 svaki vodonik.
11. Jedinjenje prema bilo kom od zahteva 1-10, u kojem najmanje oko 85% jedinjenja ima atom deuterijuma na svakom položaju označenom kao deuterijum, a svaki atom koji nije označen kao deuterijum prisutan je otprilike u svojoj prirodnoj izotopskoj rasprostranjenosti.
12. Jedinjenje prema bilo kom od zahteva 1-11, u kojem najmanje oko 90% jedinjenja ima atom deuterijuma na svakom položaju označenom kao deuterijum, a svaki atom koji nije označen kao deuterijum prisutan je otprilike u svojoj prirodnoj izotopskoj rasprostranjenosti.
13. Jedinjenje prema zahtevu 1, gde je jedinjenje hidrogen tartaratna so
14. Jedinjenje prema zahtevu 13, u kojem jedinjenje postoji u polimorfnom obliku koji ima XRPD difrakcioni obrazac kakav je prikazan na Fig. 18.
15. Jedinjenje prema zahtevu 13, u kojem najmanje oko 85% jedinjenja ima atom deuterijuma na svakom položaju označenom kao deuterijum, a svaki atom koji nije označen kao deuterijum prisutan je otprilike u svojoj prirodnoj izotopskoj rasprostranjenosti.
16. Farmaceutska kompozicija koja obuhvata jedinjenje prema bilo kom od zahteva 1 do 15 i jedan ili više farmaceutski prihvatljivih nosača, razblaživača ili ekscipijenasa.
17. Farmaceutska kompozicija prema zahtevu 16, gde je jedinjenje hidrogen tartaratna so
18. Kompozicija prema zahtevima 16 ili 17, u kojoj nosač obuhvata hidroksipropil-β-ciklodekstrin u vodi, i u kojoj najmanje oko 85% jedinjenja ima atom deuterijuma na svakom položaju označenom kao deuterijum, a svaki atom koji nije označen kao deuterijum prisutan je otprilike u svojoj prirodnoj izotopskoj rasprostranjenosti.
19. Upotreba jedinjenja prema bilo kom od zahteva 1-15, ili kompozicija prema bilo kom od zahteva 16-18 za proizvodnju leka za tretiranje psihoze, ostalih bolesti koje uključuju psihotične simptome, psihotičnih poremećaja ili bolesti koje su prisutne sa psihotičnim simptomima.
20. Upotreba prema zahtevu 19, pri čemu je psihoza ili bolest koja uključuje psihotične simptome šizofrenija, šizofreniformni poremećaj, šizoafektivni poremećaj, deluzioni poremećaj, kratkotrajni psihotični poremećaj, podeljeni psihotični poremećaj, bipolarni poremećaj ili manija u bipolarnom poremećaju.
21. Upotreba prema bilo kom od zahteva 19-20, koja dalje obuhvata jedinjenje odabrano iz grupe koja se sastoji od sertindola, olanzapina, risperidona, kvetiapina, aripiprazola, haloperidola, klozapina, ziprasidona i osanetanta.
22. Upotreba prema bilo kom od zahteva 19-20, gde je psihoza ili bolest koja uključuje psihotične simptome šizofrenija.
23. Upotreba prema bilo kom od zahteva 19-20, gde je psihoza ili bolest koja uključuje psihotične simptome šizofrenija, pri čemu farmaceutska kompozicija obuhvata efektivnu količinu hidrogen tartaratne soli i hidroksipropil-β-ciklodekstrin u vodi, i gde najmanje oko 85% (IV) ima atom deuterijuma na svakom položaju označenom kao deuterijum, a svaki atom koji nije označen kao deuterijum prisutan je otprilike u svojoj prirodnoj izotopskoj rasprostranjenosti.
24. Jedinjenje formule
25. Postupak za pripremanje jedinjenja koji obuhvata tretiranje jedinjenja (XIV) sa [(S)-BINAP]Rh(I)BF4.
26. Postupak prema zahtevu 25, u kojem se [(S)-BINAP]Rh(I)BF4 primenjuje u katalitičkoj količini.
27. Postupak za pripremanje jedinjenja (XIV) koji obuhvata a) tretiranje bis(pinakolato) diboronom, i b) tretiranje 2-bromo-5-hlorobenzaldehidom.
28. Postupak prema zahtevu 27, u kojem tretiranje bis(pinakolato) diboronom dalje obuhvata dodavanje Pd(II).
29. Postupak prema zahtevu 28, u kojem tretiranje 2-bromo-5-hlorobenzaldehidom dalje obuhvata dodavanje Pd(0).
30. Postupak za pripremanje jedinjenja (1R,3S)-(IV) tartarat, koji obuhvata tretiranje racemskog trans-1-(6-hloro-3-fenil(d5)-indan-1-il)-1(d3), 2, 2-trimetil-piperazina L-(+)-vinskom kiselinom.
31. Postupak prema zahtevu 30, u kojem se racemski trans-1-(6-hloro-3-fenil(d5)-indan-1-il)-1(d3), 2, 2-trimetil-piperazin generiše iz njegove odgovarajuće sukcinatne soli.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
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US201161498651P | 2011-06-20 | 2011-06-20 | |
US201161537103P | 2011-09-21 | 2011-09-21 | |
EP12748046.5A EP2720989B1 (en) | 2011-06-20 | 2012-06-19 | Deuterated 1-piperazino-3-phenyl indanes for treatment of schizophrenia |
PCT/IB2012/001386 WO2012176066A1 (en) | 2011-06-20 | 2012-06-19 | Deuterated 1-piperazino-3-phenyl indanes for treatment of schizophrenia |
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ME02513B true ME02513B (me) | 2017-02-20 |
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MEP-2016-226A ME02513B (me) | 2011-06-20 | 2012-06-19 | Deuterizovani 1-piperazino-3-fenil indani za tretiranje šizofrenije |
MEP-2019-93A ME03375B (me) | 2011-06-20 | 2012-06-19 | Deuterizovani 1-piperazin0-3-fenil indani za tretiranje šizofrenije |
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MEP-2019-93A ME03375B (me) | 2011-06-20 | 2012-06-19 | Deuterizovani 1-piperazin0-3-fenil indani za tretiranje šizofrenije |
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KR101879474B1 (ko) * | 2011-06-20 | 2018-07-17 | 하. 룬드벡 아크티에셀스카브 | 정신 분열증의 치료를 위한 중수소화 1-피페라지노-3-페닐 인단 |
AR094054A1 (es) * | 2012-12-19 | 2015-07-08 | H Lundbeck As | 6-cloro-3-(fenil-d₅)-inden-1-ona y uso de la misma |
WO2019049918A1 (en) | 2017-09-07 | 2019-03-14 | Otsuka Pharmaceutical Co., Ltd. | INDUSTRIAL PROCESS FOR MONOALKYLATION OF PIPERIDINE NITROGEN IN PIPERIDINE DERIVATIVES WITH DEUTERATED ALKYL |
JP7442538B2 (ja) | 2018-10-29 | 2024-03-04 | ハー・ルンドベック・アクチエゼルスカベット | 非晶性の式(i)の化合物及び非晶性の式(i)の化合物塩 |
CN113056457A (zh) | 2018-12-03 | 2021-06-29 | H.隆德贝克有限公司 | 4-((1R,3S)-6-氯-3-苯基-2,3-二氢-1H-茚-1-基)-1,2,2-三甲基哌嗪和4-((1R,3S)-6-氯-3-(苯基-d5)-2,3-二氢-1H-茚-1-基)-2,2-二甲基-1-(甲基-d3)哌嗪的前药 |
WO2020132461A1 (en) * | 2018-12-21 | 2020-06-25 | Concert Pharmaceuticals, Inc. | Deuterated forms and derivatives of volinanserin |
KR20210139317A (ko) * | 2019-03-13 | 2021-11-22 | 오츠카 세이야쿠 가부시키가이샤 | 2급 아민을 함유하는 화합물의 아민 부분에 중수소 저급 알킬을 도입하는 방법 |
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