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AR068349A1 - PROSTAGLANDIN AGONIST POLYMORPHES AND PROCEDURES TO MANUFACTURE THE SAME - Google Patents

PROSTAGLANDIN AGONIST POLYMORPHES AND PROCEDURES TO MANUFACTURE THE SAME

Info

Publication number
AR068349A1
AR068349A1 ARP080103712A ARP080103712A AR068349A1 AR 068349 A1 AR068349 A1 AR 068349A1 AR P080103712 A ARP080103712 A AR P080103712A AR P080103712 A ARP080103712 A AR P080103712A AR 068349 A1 AR068349 A1 AR 068349A1
Authority
AR
Argentina
Prior art keywords
crystalline form
diffraction pattern
powder
ray diffraction
values measured
Prior art date
Application number
ARP080103712A
Other languages
Spanish (es)
Original Assignee
Pfizer Prod Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Pfizer Prod Inc filed Critical Pfizer Prod Inc
Publication of AR068349A1 publication Critical patent/AR068349A1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic 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
    • C07D213/02Heterocyclic 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
    • C07D213/04Heterocyclic 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
    • C07D213/60Heterocyclic 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
    • C07D213/62Oxygen or sulfur atoms
    • C07D213/70Sulfur atoms
    • C07D213/71Sulfur atoms to which a second hetero atom is attached
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4406Non condensed pyridines; Hydrogenated derivatives thereof only substituted in position 3, e.g. zimeldine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/08Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • A61P19/10Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline 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

La presente se refiere a formas cristalinas polimorficas o a una forma no cristalina o amorfa del compuesto sal sodica del ácido (3-(((4-terc-butil-bencil)-(piridin-3-sulfonil)-amino)-metil)-fenoxi)-acético o un hidrato del mismo conjuntamente con procedimientos para preparar, procedimientos para usar, y composiciones farmacéuticas que contengan las mismas. La invencion se refiere también a formas cristalinas polimorficas sustancialmente puras o una forma no cristalina o forma amorfa de la sal sádica del ácido (3-(((4-terc-butil-bencil)-(piridin-3-sulfonil)-amino)-metil)-fenoxi)-acético o de un hidrato de la misma. Reivindicacion 1: Una forma cristalina de la sal sodica del ácido (3-(((4-terc-butil-bencil)- (piridin-3-sulfonil)-amino)-metil)-fenoxi)-acético o un hidrato de la misma. Reivindicacion 3: La forma cristalina de acuerdo con la reivindicacion 1, en la que: la forma cristalina es forma cristalina A; y el patron de difraccion de rayos X en polvo contiene los siguientes valores de 2 theta medidos usando radiacion de CuKalfa: 3,2, 4,1, 16,1, 20,2 y 20,8. Reivindicacion 6: La forma cristalina de acuerdo con la reivindicacion 1, en la que: la forma cristalina es forma cristalina B; y el patron de difraccion de rayos X en polvo contiene los siguientes valores de 2 theta medidos usando radiacion de CuKalfa: 3,2, 3,6, 7,1, 8,4 y 13,8. Reivindicacion 9: La forma cristalina de acuerdo con la reivindicacion 1, en la que: la forma cristalina es forma cristalina C; y el patron de difraccion de rayos X en polvo contiene los siguientes valores de 2 theta medidos usando radiacion de CuKalfa: 3,2, 4,0, 5,9, 13,3 y 16,9. Reivindicacion 12: La forma cristalina de acuerdo con la reivindicacion 1, en la que: la forma cristalina es forma cristalina E; y el patron de difraccion de rayos X en polvo contiene los siguientes valores de 2 theta medidos usando radiacion de CuKalfa: 7,0, 14,1, 21,2, 20,2 y 28,5. Reivindicacion 14: La forma cristalina de acuerdo con la reivindicacion 1, en la que: la forma cristalina es forma cristalina F; y el patron de difraccion de rayos X en polvo contiene los siguientes valores de 2 theta medidos usando radiacion de CuKalfa: 5,5, 8,2, 11,0, 19,2 y 27,5. Reivindicacion 16: La forma cristalina de acuerdo con a reivindicacion 1, en la que: la forma cristalina es forma cristalina G; y el patron de difraccion de rayos X en polvo contiene los siguientes valores de 2 theta medidos usando radiacion de CuKalfa: 3,2, 4,0, 7,9, 10,0 y 13,1. Reivindicacion 26: Una forma no cristalina de la sal sodica del ácido (3-(((4-terc-butil-bencil)-(piridin-3-sulfonil)-amino)-metil)-fenoxi)-acético o un hidrato de la misma, en la que la forma no cristalina es forma no cristalina H; y el patron de difraccion en polvo de rayos X contiene los siguientes valores de 2 theta medidos usando radiacion de CuKalfa,: 3,1. Reivindicacion 28: Una forma amorfa de la sal sodica del ácido (3-(((4-terc-butil-bencil)-(piridin-3-sulfonil)-amino)-metil)-fenoxi)-acético o un hidrato de la misma, en la que la forma amorfa es forma amorfa I; y el patron de difraccion de rayos X es sustancialmente como se muestra en la figura 6C.This refers to polymorphic crystalline forms or a non-crystalline or amorphous form of the compound sodium salt of the acid (3 - (((4-tert-butyl-benzyl) - (pyridin-3-sulfonyl) -amino) -methyl) - phenoxy) -acetic acid or a hydrate thereof in conjunction with methods for preparing, procedures for use, 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 the sadic acid salt (3 - (((4-tert-butyl-benzyl) - (pyridin-3-sulfonyl) -amino) -methyl) -phenoxy) -acetic acid or a hydrate thereof. Claim 1: A crystalline form of the sodium salt of the (3 - (((4-tert-butyl-benzyl) - (pyridin-3-sulfonyl) -amino) -methyl) -phenoxy) -acetic acid or a hydrate of the same. Claim 3: The crystalline form according to claim 1, wherein: the crystalline form is crystalline form A; and the powder X-ray diffraction pattern contains the following 2 theta values measured using CuKalfa radiation: 3.2, 4.1, 16.1, 20.2 and 20.8. Claim 6: The crystalline form according to claim 1, wherein: the crystalline form is crystalline form B; and the powder X-ray diffraction pattern contains the following 2 theta values measured using CuKalfa radiation: 3.2, 3.6, 7.1, 8.4 and 13.8. Claim 9: The crystalline form according to claim 1, wherein: the crystalline form is crystalline form C; and the powder X-ray diffraction pattern contains the following 2 theta values measured using CuKalfa radiation: 3.2, 4.0, 5.9, 13.3 and 16.9. Claim 12: The crystalline form according to claim 1, wherein: the crystalline form is crystalline form E; and the powder X-ray diffraction pattern contains the following 2 theta values measured using CuKalfa radiation: 7.0, 14.1, 21.2, 20.2 and 28.5. Claim 14: The crystalline form according to claim 1, wherein: the crystalline form is crystalline form F; and the powder X-ray diffraction pattern contains the following 2 theta values measured using CuKalfa radiation: 5.5, 8.2, 11.0, 19.2 and 27.5. Claim 16: The crystalline form according to claim 1, wherein: the crystalline form is crystalline form G; and the powder X-ray diffraction pattern contains the following 2 theta values measured using CuKalfa radiation: 3.2, 4.0, 7.9, 10.0 and 13.1. Claim 26: A non-crystalline form of the sodium salt of the (3 - (((4-tert-butyl-benzyl) - (pyridin-3-sulfonyl) -amino) -methyl) -phenoxy) -acetic acid or a hydrate of the same, in which the non-crystalline form is non-crystalline form H; and the X-ray powder diffraction pattern contains the following 2 theta values measured using CuKalfa radiation: 3.1. Claim 28: An amorphous form of the sodium salt of the (3 - (((4-tert-butyl-benzyl) - (pyridin-3-sulfonyl) -amino) -methyl) -phenoxy) -acetic acid or a hydrate of the same, in which the amorphous form is amorphous form I; and the X-ray diffraction pattern is substantially as shown in Figure 6C.

ARP080103712A 2007-08-29 2008-08-27 PROSTAGLANDIN AGONIST POLYMORPHES AND PROCEDURES TO MANUFACTURE THE SAME AR068349A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US96877107P 2007-08-29 2007-08-29
US8355908P 2008-07-25 2008-07-25

Publications (1)

Publication Number Publication Date
AR068349A1 true AR068349A1 (en) 2009-11-11

Family

ID=40042625

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP080103712A AR068349A1 (en) 2007-08-29 2008-08-27 PROSTAGLANDIN AGONIST POLYMORPHES AND PROCEDURES TO MANUFACTURE 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)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102356080B (en) 2009-02-27 2015-04-29 奥索-麦克尼尔-詹森药品公司 Amorphous salts of HCV macrocyclic inhibitors
KR102058853B1 (en) * 2018-02-28 2019-12-24 브릿지바이오테라퓨틱스(주) Water soluble salts of lipidated peptides and methods for preparing and using the same

Family Cites Families (1)

* Cited by examiner, † Cited by third party
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

Also Published As

Publication number Publication date
CA2697950A1 (en) 2009-03-05
EP2185516A2 (en) 2010-05-19
JP2009137934A (en) 2009-06-25
KR20100050559A (en) 2010-05-13
AU2008291814A1 (en) 2009-03-05
MX2010002300A (en) 2010-03-18
WO2009027811A2 (en) 2009-03-05
CN101842356A (en) 2010-09-22
WO2009027811A3 (en) 2009-06-11

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