MX2010002300A - Polymorphs of 3- ( ( (4-tert-butyl-benzyl) - (pyridine-3-sulfonyl ) -amino) -methyl) -phenoxy) -acetic acid sodium salt or a hydrate thereof and methods for making the same. - Google Patents
Polymorphs of 3- ( ( (4-tert-butyl-benzyl) - (pyridine-3-sulfonyl ) -amino) -methyl) -phenoxy) -acetic acid sodium salt or a hydrate thereof and methods for making the same.Info
- Publication number
- MX2010002300A MX2010002300A MX2010002300A MX2010002300A MX2010002300A MX 2010002300 A MX2010002300 A MX 2010002300A MX 2010002300 A MX2010002300 A MX 2010002300A MX 2010002300 A MX2010002300 A MX 2010002300A MX 2010002300 A MX2010002300 A MX 2010002300A
- Authority
- MX
- Mexico
- Prior art keywords
- sulfonyl
- hydrate
- pyridine
- tert
- benzyl
- Prior art date
Links
- -1 3- ( ( (4-tert-butyl-benzyl) - (pyridine-3-sulfonyl ) -amino) -methyl) -phenoxy Chemical group 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- SVNBMCJEDANCKY-UHFFFAOYSA-M sodium;2-[3-[[(4-tert-butylphenyl)methyl-pyridin-3-ylsulfonylamino]methyl]phenoxy]acetate Chemical compound [Na+].C1=CC(C(C)(C)C)=CC=C1CN(S(=O)(=O)C=1C=NC=CC=1)CC1=CC=CC(OCC([O-])=O)=C1 SVNBMCJEDANCKY-UHFFFAOYSA-M 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/62—Oxygen or sulfur atoms
- C07D213/70—Sulfur atoms
- C07D213/71—Sulfur atoms to which a second hetero atom is attached
-
- 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
- A61K31/4406—Non condensed pyridines; Hydrogenated derivatives thereof only substituted in position 3, e.g. zimeldine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Physical Education & Sports Medicine (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Rheumatology (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
Abstract
The present invention relates to polymorphic crystalline forms or a non- crystalline form or amorphous of the compound (3-(((4-tert-butyl-benzyl)-(pyridine- 3-sulfonyl)-amino)-methyl)-phenoxy)-acetic acid sodium salt or a hydrate thereof together with processes for preparing, methods for using, and pharmaceutical compositions containing the same. The invention also relates to substantially pure polymorphic crystalline forms or a non-crystalline form or amorphous form of (3- (((4-tert-butyl-benzyl)-(pyridine-3-sulfonyl)-amino)-methyl)-ph enoxy)-acetic acid sodium salt or a hydrate thereof.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US96877107P | 2007-08-29 | 2007-08-29 | |
| US8355908P | 2008-07-25 | 2008-07-25 | |
| PCT/IB2008/002252 WO2009027811A2 (en) | 2007-08-29 | 2008-08-25 | Polymorphs of 3- ( ( (4-tert-butyl-benzyl) - (pyridine-3-sulfonyl) -amino) -methyl) -phenoxy) -acetic acid sodium salt or a hydrate thereof and methods for making the same |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MX2010002300A true MX2010002300A (en) | 2010-03-18 |
Family
ID=40042625
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2010002300A MX2010002300A (en) | 2007-08-29 | 2008-08-25 | Polymorphs of 3- ( ( (4-tert-butyl-benzyl) - (pyridine-3-sulfonyl ) -amino) -methyl) -phenoxy) -acetic acid sodium salt or a hydrate thereof and methods for making the same. |
Country Status (9)
| Country | Link |
|---|---|
| EP (1) | EP2185516A2 (en) |
| JP (1) | JP2009137934A (en) |
| KR (1) | KR20100050559A (en) |
| CN (1) | CN101842356A (en) |
| AR (1) | AR068349A1 (en) |
| AU (1) | AU2008291814A1 (en) |
| CA (1) | CA2697950A1 (en) |
| MX (1) | MX2010002300A (en) |
| WO (1) | WO2009027811A2 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104478868A (en) * | 2009-02-27 | 2015-04-01 | 奥索-麦克尼尔-詹森药品公司 | Amorphous salt of a macrocyclic inhibitor of HCV |
| TWI762770B (en) * | 2018-02-28 | 2022-05-01 | 韓商畢利吉生物科技股份有限公司 | Water soluble salts of lipidated peptides and methods for preparing and using the same |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| UA67754C2 (en) * | 1997-10-10 | 2004-07-15 | Пфайзер, Інк. | Prostaglandin agonists and use thereof for the treatment of bone disorders |
-
2008
- 2008-08-25 MX MX2010002300A patent/MX2010002300A/en not_active Application Discontinuation
- 2008-08-25 WO PCT/IB2008/002252 patent/WO2009027811A2/en not_active Ceased
- 2008-08-25 CA CA2697950A patent/CA2697950A1/en not_active Abandoned
- 2008-08-25 AU AU2008291814A patent/AU2008291814A1/en not_active Abandoned
- 2008-08-25 EP EP08806952A patent/EP2185516A2/en not_active Withdrawn
- 2008-08-25 KR KR1020107006782A patent/KR20100050559A/en not_active Ceased
- 2008-08-25 CN CN200880113737A patent/CN101842356A/en active Pending
- 2008-08-27 AR ARP080103712A patent/AR068349A1/en not_active Application Discontinuation
- 2008-08-28 JP JP2008218939A patent/JP2009137934A/en not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| AU2008291814A1 (en) | 2009-03-05 |
| AR068349A1 (en) | 2009-11-11 |
| EP2185516A2 (en) | 2010-05-19 |
| CA2697950A1 (en) | 2009-03-05 |
| KR20100050559A (en) | 2010-05-13 |
| JP2009137934A (en) | 2009-06-25 |
| WO2009027811A2 (en) | 2009-03-05 |
| CN101842356A (en) | 2010-09-22 |
| WO2009027811A3 (en) | 2009-06-11 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| WO2007141283A3 (en) | Salts and crystalline salt forms of an 2-indolinone derivative | |
| WO2010001257A3 (en) | Novel solid state forms of laquinimod and its sodium salt | |
| TN2012000248A1 (en) | Novel spiropiperidine compounds | |
| WO2008155615A3 (en) | An improved process for the preparation of cephalosporin antibiotic | |
| MX2012013332A (en) | Preparation of posaconazole intermediates. | |
| WO2012138147A3 (en) | 1-(3-cyano-1-isopropyl-indol-5-yl)pyrazole-4-carboxylic acid crystalline form and the producing method thereof | |
| MX2009003257A (en) | Process for synthesis of phenoxy diaminopyrimidine derivatives. | |
| WO2013014665A8 (en) | Intermediate compounds and process for the preparation of lurasidone and salts thereof | |
| MX2011007978A (en) | Novel method for the synthesis of ivabradine and the pharmaceutically acceptable acid addition salts thereof. | |
| MX2011009898A (en) | Process for the preparation of propionic acid derivatives. | |
| WO2010070677A3 (en) | A process for the preparation of prasugrel and its pharmaceutically acceptable salts thereof | |
| MY161749A (en) | Compound, certain novel forms thereof, pharmaceutical compositions thereof and methods for preparation and use | |
| EA201300647A1 (en) | OPTIMIZED SYNTHESIS OF PURE NONPOLYMORPHIC CRYSTALLINE YELLOW ACIDS WITH A PARTICLE SIZE | |
| MX2009005911A (en) | Crystalline potassium salt of lipoxin a4 analogs. | |
| MX2010003213A (en) | Novel method for the synthesis of ivabradine and the addition salts thereof with a pharmaceutically acceptable acid. | |
| WO2008117305A3 (en) | A novel process for preparing pregabalin and its acid addition salts | |
| WO2010079045A3 (en) | Crystalline salt forms of flibanserine | |
| MX2012002818A (en) | Novel method for synthesizing ivabradine and the addition salts thereof with a pharmaceutically acceptable acid. | |
| WO2011008666A3 (en) | 3-phenoxymethylpyrrolidine compounds | |
| WO2008015703A3 (en) | Process for the preparation of montelukast and its salts thereof | |
| MX2010009926A (en) | New process for the preparatiion of cyclohexanecarboxylic acid dericatives. | |
| WO2008081476A3 (en) | Process for preparing duloxetine hydrochloride | |
| MX337997B (en) | New method for synthesising ivabradine and its added salts with a pharmaceutically acceptable acid. | |
| WO2011135586A3 (en) | Process for the preparation of chiral beta amino carboxamide derivatives | |
| MX2010002300A (en) | Polymorphs of 3- ( ( (4-tert-butyl-benzyl) - (pyridine-3-sulfonyl ) -amino) -methyl) -phenoxy) -acetic acid sodium salt or a hydrate thereof and methods for making the same. |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FA | Abandonment or withdrawal |