ES2572652T3 - Nuevas formas de un compuesto multicíclico - Google Patents
Nuevas formas de un compuesto multicíclico Download PDFInfo
- Publication number
- ES2572652T3 ES2572652T3 ES10750210.6T ES10750210T ES2572652T3 ES 2572652 T3 ES2572652 T3 ES 2572652T3 ES 10750210 T ES10750210 T ES 10750210T ES 2572652 T3 ES2572652 T3 ES 2572652T3
- Authority
- ES
- Spain
- Prior art keywords
- new forms
- compound
- multicyclic compound
- theta
- degrees
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- 150000001875 compounds Chemical class 0.000 title abstract description 4
- 238000000634 powder X-ray diffraction Methods 0.000 abstract description 7
- 239000000203 mixture Substances 0.000 abstract 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 2
- DKPFZGUDAPQIHT-UHFFFAOYSA-N butyl acetate Chemical compound CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- 101100514821 Caenorhabditis elegans dsc-4 gene Proteins 0.000 description 1
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- DHXVGJBLRPWPCS-UHFFFAOYSA-N Tetrahydropyran Chemical compound C1CCOCC1 DHXVGJBLRPWPCS-UHFFFAOYSA-N 0.000 description 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- WBJINCZRORDGAQ-UHFFFAOYSA-N formic acid ethyl ester Natural products CCOC=O WBJINCZRORDGAQ-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 150000004677 hydrates Chemical class 0.000 description 1
- JMMWKPVZQRWMSS-UHFFFAOYSA-N isopropanol acetate Natural products CC(C)OC(C)=O JMMWKPVZQRWMSS-UHFFFAOYSA-N 0.000 description 1
- 229940011051 isopropyl acetate Drugs 0.000 description 1
- GWYFCOCPABKNJV-UHFFFAOYSA-N isovaleric acid Chemical compound CC(C)CC(O)=O GWYFCOCPABKNJV-UHFFFAOYSA-N 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
- FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 1
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- 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
- A61K31/4965—Non-condensed pyrazines
- A61K31/497—Non-condensed pyrazines containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- 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
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Steroid Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Hydrogenated Pyridines (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
Forma cristalina del Compuesto I que tiene la Fórmula**Fórmula** en donde la forma cristalina es: (A) a. la Forma A0 se caracteriza por un patrón de difracción de rayos X de polvo que comprende uno o más de los siguientes picos: 4.32, 6.07, 8.55, 12.07 y 15.37 ± 0.2 grados 2-theta; o (B) a. la Forma HC0 se caracteriza por un patrón de difracción de rayos X de polvo que comprende uno o más de los siguientes picos: 8.36, 8.71, 16.69, 17.39 y 24.59 ± 0.2 grados 2-theta; o b. la Forma HD0 se caracteriza por un patrón de difracción de rayos X de polvo que comprende uno o más de los siguientes picos: 7.60, 8.99 y 15.16 ± 0.2 grados 2-theta; o una mezcla de estos.
Description
(Continúa)
- Disolvente
- Formas obtenidas por XRPD
- Diisopropil éter
- A0, HA0, HC0, HD0
- Dimetilsulfóxido
- HC0, HD0
- Etanol
- S40
- Acetato de etilo
- A0, HC0, HD0
- Formiato de etilo
- HA0
- Etilenglicol
- S60
- Heptano
- A0, HC0, HD0
- Isobutanol
- S120, HD0
- Acetato de isopropilo
- A0, HC0, HD0
- Metanol
- S20
- Metoxibenceno
- HD0
- Acetato de metilo
- A0, HA0, HC0, HD0
- Metil isobutil cetona
- A0, HC0, HD0
- Metil terc-butil éter
- A0, HA0, HC0, HD0
- N,N-dimetilacetamida
- S100
- N,N-dimetilformamida
- S50
- Acetato de N-butilo
- A0, HC0, HD0
- Propanonitrilo
- A0, HA0, HC0, HD0
- Carbonato de propileno
- A0, HC0, HD0
- Piridina
- S70
- Terc-butanol
- A0, HC0, HD0
- Tetrahidrofurano
- A0, HC0, HD0
- Tetrahidropirano
- HC0, HD0
- Tolueno
- A0, HC0, HD0
- Trietilamina
- HC0, HD0
- Agua
- A0, HA0, HC0, HD0
- Xileno
- A0, HA0, BC0, HD0
Tabla 16: Datos de la caracterización de las formas aisladas del Compuesto I
5
10
15
20
25
30
35
40
El tamizaje de polimorfos del Compuesto I rindió catorce formas y una nueva forma (Forma B0) obtenidas solo al 45 calentar los hidratos por encima de 120 °C. Un resumen de los resultados de las formas aisladas se muestra en la Tabla 16más abajo.
EstabilidadEstabilidad física
50 TGA química (HPLC DVS % del XRPD
(XRPD después
(pérdida de después de 4 aumento en después del PurezaForma XRPD DSC de 4 semanas a peso 25 °C semanas a 40 masa a 90 análisis de (%)
40 °C/75 % de
a 150 °C) °C/75 % de HR (%% de HR DVS
HR)
de Área) 55
Endoterma Sin cambios Sin cambios
A0 Cristalina de fusión a 0.07 % 99.0 0.1 99.2
significativos significativos239.7 °C
Endoterma 60 B0 Cristalina defusióna -----
199.8 °C
21
Claims (1)
-
imagen1
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US237180P | 2000-10-03 | ||
US23718009P | 2009-08-26 | 2009-08-26 | |
PCT/US2010/046671 WO2011028580A1 (en) | 2009-08-26 | 2010-08-25 | Novel forms of a multicyclic compound |
Publications (1)
Publication Number | Publication Date |
---|---|
ES2572652T3 true ES2572652T3 (es) | 2016-06-01 |
Family
ID=43033463
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES10750210.6T Active ES2572652T3 (es) | 2009-08-26 | 2010-08-25 | Nuevas formas de un compuesto multicíclico |
Country Status (20)
Country | Link |
---|---|
US (1) | US8633314B2 (es) |
EP (1) | EP2470540B1 (es) |
JP (3) | JP2013503173A (es) |
KR (1) | KR20120092100A (es) |
CN (1) | CN102482282A (es) |
AU (1) | AU2010289746B2 (es) |
BR (1) | BR112012004053A2 (es) |
CA (1) | CA2772328C (es) |
CL (1) | CL2012000478A1 (es) |
DK (1) | DK2470540T3 (es) |
EA (1) | EA020756B1 (es) |
ES (1) | ES2572652T3 (es) |
HK (1) | HK1171750A1 (es) |
IL (1) | IL218132B (es) |
MX (1) | MX2012002456A (es) |
MY (1) | MY156873A (es) |
NZ (1) | NZ598883A (es) |
SG (1) | SG178852A1 (es) |
UA (1) | UA110604C2 (es) |
WO (1) | WO2011028580A1 (es) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SG178852A1 (en) * | 2009-08-26 | 2012-04-27 | Cephalon Inc | Novel forms of a multicyclic compound |
US10150772B2 (en) * | 2014-11-26 | 2018-12-11 | Cephalon, Inc. | Crystalline forms of PARP inhibitors |
MX2019011496A (es) | 2017-03-27 | 2020-01-23 | Tesaro Inc | Composiciones de niraparib. |
AU2018341479B2 (en) | 2017-09-26 | 2022-02-17 | Tesaro, Inc. | Niraparib formulations |
CN109632555B (zh) * | 2018-12-28 | 2021-07-27 | 上海新黄河制药有限公司 | 一种富马酸福莫特罗无定型含量的动态蒸汽吸附分析方法 |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20060276497A1 (en) * | 2000-05-09 | 2006-12-07 | Cephalon, Inc. | Novel multicyclic compounds and the use thereof |
US7122679B2 (en) * | 2000-05-09 | 2006-10-17 | Cephalon, Inc. | Multicyclic compounds and the use thereof |
CA2620052A1 (en) * | 2005-08-24 | 2007-03-01 | Inotek Pharmaceuticals Corporation | Indenoisoquinolinone analogs and methods of use thereof |
CA2671517C (en) | 2006-11-20 | 2015-01-27 | Cephalon, Inc. | Method of radio-sensitizing tumors using a radio-sensitizing agent |
SG178852A1 (en) * | 2009-08-26 | 2012-04-27 | Cephalon Inc | Novel forms of a multicyclic compound |
-
2010
- 2010-08-25 SG SG2012012290A patent/SG178852A1/en unknown
- 2010-08-25 CA CA2772328A patent/CA2772328C/en not_active Expired - Fee Related
- 2010-08-25 ES ES10750210.6T patent/ES2572652T3/es active Active
- 2010-08-25 KR KR1020127007524A patent/KR20120092100A/ko not_active Application Discontinuation
- 2010-08-25 JP JP2012526945A patent/JP2013503173A/ja active Pending
- 2010-08-25 CN CN2010800380284A patent/CN102482282A/zh active Pending
- 2010-08-25 EA EA201270315A patent/EA020756B1/ru not_active IP Right Cessation
- 2010-08-25 MX MX2012002456A patent/MX2012002456A/es active IP Right Grant
- 2010-08-25 BR BR112012004053-7A patent/BR112012004053A2/pt not_active IP Right Cessation
- 2010-08-25 WO PCT/US2010/046671 patent/WO2011028580A1/en active Application Filing
- 2010-08-25 AU AU2010289746A patent/AU2010289746B2/en not_active Ceased
- 2010-08-25 MY MYPI2012000710A patent/MY156873A/en unknown
- 2010-08-25 NZ NZ598883A patent/NZ598883A/en not_active IP Right Cessation
- 2010-08-25 DK DK10750210.6T patent/DK2470540T3/en active
- 2010-08-25 UA UAA201203501A patent/UA110604C2/uk unknown
- 2010-08-25 EP EP10750210.6A patent/EP2470540B1/en active Active
-
2012
- 2012-02-15 IL IL218132A patent/IL218132B/en not_active IP Right Cessation
- 2012-02-24 US US13/404,137 patent/US8633314B2/en not_active Expired - Fee Related
- 2012-02-24 CL CL2012000478A patent/CL2012000478A1/es unknown
- 2012-12-06 HK HK12112589.8A patent/HK1171750A1/zh not_active IP Right Cessation
-
2015
- 2015-07-30 JP JP2015151114A patent/JP2016014029A/ja not_active Ceased
-
2017
- 2017-09-04 JP JP2017169876A patent/JP2018035158A/ja not_active Withdrawn
Also Published As
Publication number | Publication date |
---|---|
WO2011028580A1 (en) | 2011-03-10 |
MY156873A (en) | 2016-04-15 |
CN102482282A (zh) | 2012-05-30 |
KR20120092100A (ko) | 2012-08-20 |
CL2012000478A1 (es) | 2012-11-05 |
HK1171750A1 (zh) | 2013-04-05 |
JP2016014029A (ja) | 2016-01-28 |
SG178852A1 (en) | 2012-04-27 |
AU2010289746A1 (en) | 2012-04-12 |
UA110604C2 (uk) | 2016-01-25 |
EA201270315A1 (ru) | 2012-08-30 |
EP2470540A1 (en) | 2012-07-04 |
DK2470540T3 (en) | 2016-08-01 |
JP2018035158A (ja) | 2018-03-08 |
NZ598883A (en) | 2014-09-26 |
US8633314B2 (en) | 2014-01-21 |
EP2470540B1 (en) | 2016-04-20 |
AU2010289746B2 (en) | 2016-07-07 |
IL218132A0 (en) | 2012-06-28 |
EA020756B1 (ru) | 2015-01-30 |
IL218132B (en) | 2018-02-28 |
BR112012004053A2 (pt) | 2020-12-08 |
CA2772328A1 (en) | 2011-03-10 |
MX2012002456A (es) | 2012-05-08 |
JP2013503173A (ja) | 2013-01-31 |
CA2772328C (en) | 2017-06-20 |
US20120214998A1 (en) | 2012-08-23 |
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