PE20080353A1 - SALTS OF 8 - [{1- (3,5-BIS- (TRIFLUOROMETIL) PHENYL) -ETOXY} -METIL] -8-PHENYL-1,7-DIAZA-ESPIRO [4,5] DECAN-2-ONA AND PROCESS OF PREPARING THEM - Google Patents
SALTS OF 8 - [{1- (3,5-BIS- (TRIFLUOROMETIL) PHENYL) -ETOXY} -METIL] -8-PHENYL-1,7-DIAZA-ESPIRO [4,5] DECAN-2-ONA AND PROCESS OF PREPARING THEMInfo
- Publication number
- PE20080353A1 PE20080353A1 PE2007000415A PE2007000415A PE20080353A1 PE 20080353 A1 PE20080353 A1 PE 20080353A1 PE 2007000415 A PE2007000415 A PE 2007000415A PE 2007000415 A PE2007000415 A PE 2007000415A PE 20080353 A1 PE20080353 A1 PE 20080353A1
- Authority
- PE
- Peru
- Prior art keywords
- phenyl
- espiro
- etoxy
- decan
- ona
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/10—Spiro-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/08—Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Otolaryngology (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Hospice & Palliative Care (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (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)
Abstract
SE REFIERE A FORMAS SALINAS CRISTALINAS DEL COMPUESTO (5S,8S)-8-[{(1R)-1-(3,5-BIS-(TRIFLUOROMETIL)FENIL-ETOXI}-METIL]-8-FENIL-1,7-DIAZA-ESPIRO[4,5]DECAN-2-ONA DE FORMULA (I), SIENDO SELECCIONADAS LA SAL CRISTALINA DE ESILATO QUE PRESENTA EL SIGUIENTES PATRON DE DIFRACCION EXPRESADOS EN ANGULOS DE DIFRACCION (2?) DE: 11.4, 12.8, 20.0, 21.2; LA SAL CRISTALINA DE OXILATO PRESENTA EL SIGUIENTE PATRON DE DIFRACCION (EXPRESADOS EN 2?) DE: 5.6, 19.8, 21.0, 22.8; LA SAL CRISTALINA DE MESILATO PRESENTA EL SIGUIENTE PATRON DE DIFRACCION: 4.7, 9.5, 19.2, 20.9; ASI TAMBIEN ES IDENTIFICADA LA SAL CRISTALINA DE MALEATO; ENTRE OTRAS SALES. TAMBIEN SE REFIERE A UN PROCEDIMIENTO DE PREPARACION Y A UNA COMPOSICION FARMACEUTICA; DICHO COMPUESTO ES UN ANTAGONISTA DEL RECEPTOR NK-1, POR LO QUE ES UTIL EN EL LA TERAPIA ANTINAUSEA Y ANTIEMESISREFERS TO CRYSTALLINE SALT FORMS OF THE COMPOUND (5S, 8S) -8 - [{(1R) -1- (3,5-BIS- (TRIFLUOROMETHYL) PHENYL-ETOXY} -Methyl] -8-PHENYL-1,7- DIAZA-ESPIRO [4,5] DECAN-2-ONA OF FORMULA (I), BEING SELECTED THE CRYSTALLINE ESILATE SALT THAT PRESENTS THE FOLLOWING PATTERN OF DIFFRACTION EXPRESSED IN ANGULES OF DIFRACTION (2?) OF: 11.4, 12.8, 20.0, 21.2; THE CRYSTALLINE SALT OF OXYLATE PRESENTS THE FOLLOWING PATTERN OF DIFFRACTION (EXPRESSED IN 2?) OF: 5.6, 19.8, 21.0, 22.8; THE CRYSTALLINE SALT OF MESILATE PRESENTS THE FOLLOWING PATTERN OF DIFFRACTION: 4.7, 9.5, 19.2, 20.9; SO CRYSTALINE MALEATE SALT IS ALSO IDENTIFIED; AMONG OTHER SALTS. IT ALSO REFERS TO A PREPARATION PROCEDURE AND A PHARMACEUTICAL COMPOSITION; SUCH COMPOUND IS AN ANTAGONIST OF THE NK-1 RECEPTOR, SO IT IS USEFUL IN ANTIEM THERAPY
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US78951306P | 2006-04-05 | 2006-04-05 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20080353A1 true PE20080353A1 (en) | 2008-04-25 |
Family
ID=38470135
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2007000415A PE20080353A1 (en) | 2006-04-05 | 2007-04-04 | SALTS OF 8 - [{1- (3,5-BIS- (TRIFLUOROMETIL) PHENYL) -ETOXY} -METIL] -8-PHENYL-1,7-DIAZA-ESPIRO [4,5] DECAN-2-ONA AND PROCESS OF PREPARING THEM |
Country Status (5)
Country | Link |
---|---|
AR (1) | AR060352A1 (en) |
CL (1) | CL2007000947A1 (en) |
PE (1) | PE20080353A1 (en) |
TW (1) | TW200806666A (en) |
WO (1) | WO2007114922A2 (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2662373A1 (en) | 2006-04-05 | 2013-11-13 | OPKO Health, Inc. | Salts of 8-[{1-(3,5-Bis-(trifluoromethyl)phenyl)-ethoxy}-methyl]-8-phenyl-1,7-diaza-spiro[4.5]decan-2-one and preparation process therefor |
AR066191A1 (en) | 2007-03-22 | 2009-08-05 | Schering Corp | PROCESS AND INTERMEDIARIES FOR THE SYNTHESIS OF COMPOUNDS 8- [(1- (3,5- BIS- (TRIFLUOROMETIL) PHENYL) - ETOXI) - METAL] - 8 PHENYL - 1,7- DIAZA - ESPIRO (4, 5) DECAN - 2 ONA |
PT2346823E (en) | 2008-09-05 | 2015-11-26 | Opko Health Inc | Intermediates for the synthesis of 8-[{1-(3,5-bis-(trifluoromethyl)phenyl)-ethoxy}-methyl]-8-phenyl-1,7-diaza-spiro[4.5]decan-2-one compounds |
CN105017251B (en) * | 2015-06-30 | 2018-06-29 | 齐鲁制药有限公司 | A kind of Preparation Method And Their Intermediate of nk 1 receptor antagonist |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
PE20030762A1 (en) * | 2001-12-18 | 2003-09-05 | Schering Corp | HETEROCYCLIC COMPOUNDS AS NK1 ANTAGONISTS |
EP1706116A1 (en) * | 2003-12-22 | 2006-10-04 | Schering Corporation | Pharmaceutical compositions |
-
2007
- 2007-04-04 PE PE2007000415A patent/PE20080353A1/en not_active Application Discontinuation
- 2007-04-04 AR ARP070101435A patent/AR060352A1/en not_active Application Discontinuation
- 2007-04-04 CL CL2007000947A patent/CL2007000947A1/en unknown
- 2007-04-04 WO PCT/US2007/008346 patent/WO2007114922A2/en active Application Filing
- 2007-04-04 TW TW096112181A patent/TW200806666A/en unknown
Also Published As
Publication number | Publication date |
---|---|
TW200806666A (en) | 2008-02-01 |
AR060352A1 (en) | 2008-06-11 |
CL2007000947A1 (en) | 2008-01-25 |
WO2007114922A2 (en) | 2007-10-11 |
WO2007114922A3 (en) | 2008-01-17 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
PE20120545A1 (en) | PHARMACEUTICAL COMPOSITION INCLUDING FORM I SALT CRYSTALLINE HYDROCHLORIDE MONOHYDRATE OF (5S, 8S) -8 - [{(1R) -1- (3,5-BIS- (TRIFLUOROMETIL) PHENYL) -ETOXY} -METIL] -8 -PHENYL-1,7-DIAZASPIRO [4,5] DECAN-2-ONA | |
PE20081650A1 (en) | COMBINATIONS INCLUDING FORMOTEROL AND SALMETEROL AND SALTS OF 3 (R) - (2-HYDROXY-2,2-DITIEN-2-ILACETOXY) -1- (3-PHENOXYPROPYL) -1-AZONIABICICLO [2,2,2] OCTANE | |
PE20081891A1 (en) | TABLET FORMULATIONS CONTAINING SALTS OF 8 - [{1- (3,5-BIS- (TRIFLUOROMETIL) PHENYL) -ETOXY} -METIL] -8-PHENYL-1,7-DIAZA-SPIRO [4.5] DECAN-2- ONA AND TABLETS MADE FROM THESE | |
WO2012101065A3 (en) | Pyrimidine biaryl amine compounds and their use as cdk9 inhibitors | |
EA201001013A1 (en) | BIS (SULFONILAMINO) DERIVATIVES FOR USE IN THERAPY | |
CO6290644A2 (en) | KAPPA SELECTIVE OPIOID RECEIVER ANTAGONIST. | |
EA201000805A1 (en) | BIS- (SULFONILAMINO) DERIVATIVES IN THERAPY 066 | |
MX2011011156A (en) | Diamide compounds having muscarinic receptor antagonist and î²2 adrenergic receptor agonist activity. | |
CL2012001517A1 (en) | Divalent and heterocyclic compounds linked by nicotine related oxa; methods of preparing them; agrochemical composition comprising said compounds. | |
AR056014A1 (en) | COMPOUND 3-AMINOCARBAZOL, PHARMACEUTICAL COMPOSITION CONTAINING IT AND PROCEDURE FOR THE PREPARATION OF THE SAME | |
PE20080054A1 (en) | PHARMACEUTICAL SALTS FORMULATIONS OF 8- [1- (3,5-BIS- (TRIFLOUROMETHYL) PHENYL) -ETOXIMETHYL] -8-PHENYL-1,7-DIAZA-SPIRO [4,5] DECAN-2-ONA | |
EA200702161A1 (en) | CRYSTAL FORM OF A QUINOLINON-CARBOXAMIDE COMPOUND | |
UY32156A (en) | SUBSTITUTED DERIVATIVES OF THE N2 - [1- (5 - FLUOROPIRIMIDIN -2-IL) ETIL] - N4 - (1-METHYL - 1H-IMIDAZOL - 4 - IL)) - PYRIMIDINE - 2,4 - DIAMINES AND THEIR PHARMACEUTICALLY ACCEPTABLE SALTS , PREPARATION PROCESS, COMPOSITIONS CONTAINING THEM AND APPLICATIONS. | |
PE20140099A1 (en) | DERIVATIVES OF AZETIDINE AND CYCLOBUTANE AS JAK INHIBITORS | |
PE20080353A1 (en) | SALTS OF 8 - [{1- (3,5-BIS- (TRIFLUOROMETIL) PHENYL) -ETOXY} -METIL] -8-PHENYL-1,7-DIAZA-ESPIRO [4,5] DECAN-2-ONA AND PROCESS OF PREPARING THEM | |
EA201101398A1 (en) | SUBSTITUTED PIPERIDINE AS AN ANTAGONIST CCR3 | |
AR058904A1 (en) | IMPROVED PROCESS FOR THE PREPARATION OF A DERIVATIVE OF 5H-PIRROLO [3,4-B] OPTICALLY ACTIVE PIRAZINE | |
SI2875011T1 (en) | 5-ht3 receptor antagonists | |
BRPI0519709A2 (en) | tetraline and indane derivatives and their use as 5-ht antagonists | |
TW200714587A (en) | Biphenyl compounds useful as muscarinic receptor antagonists | |
AR068187A1 (en) | CRYSTAL FORM OF A SYNTHETIC INTERMEDIARY FOR THE PREPARATION OF A DPP-IV INHIBITOR | |
CO6430439A2 (en) | SPHINGOSINE RECEPTOR AGONISTS -1- PHOSPHATE | |
UY31672A1 (en) | "MUSCARINIC RECEPTORS AGONISTS PHARMACEUTICAL COMPOSITIONS METHODS OF TREATMENT OF THE SAME, AND PROCEDURES FOR THEIR PREPARATION" | |
WO2012176218A8 (en) | Process for preparing rosuvastatin calcium through novel amine salt | |
AR075160A1 (en) | DERIVATIVES OF ARIL AND / OR HETEROARIL PIPERIDINES REPLACED, MEDICINES THAT CONTAIN THEM, PROCESS TO PREPARE THEM AND USE OF THE SAME FOR THE TREATMENT OF NEUROLOGICAL AND NEUROPSYCHIATRIC DISORDERS. |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FD | Application declared void or lapsed |