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PE20060216A1 - Proceso que emplea cristalizacion controlada en la formacion de cristales de un producto farmaceutico - Google Patents

Proceso que emplea cristalizacion controlada en la formacion de cristales de un producto farmaceutico

Info

Publication number
PE20060216A1
PE20060216A1 PE2005000498A PE2005000498A PE20060216A1 PE 20060216 A1 PE20060216 A1 PE 20060216A1 PE 2005000498 A PE2005000498 A PE 2005000498A PE 2005000498 A PE2005000498 A PE 2005000498A PE 20060216 A1 PE20060216 A1 PE 20060216A1
Authority
PE
Peru
Prior art keywords
reagent
crystals
pharmaceutical product
provision
crystalization
Prior art date
Application number
PE2005000498A
Other languages
English (en)
Inventor
Soojin Kim
Chenkou Wei
Mark Lindrud
Hyei-Jha Chung
Original Assignee
Bristol Myers Squibb Co
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=35320785&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PE20060216(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co
Publication of PE20060216A1 publication Critical patent/PE20060216A1/es

Links

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
    • C07D213/24—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 substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/36—Radicals substituted by singly-bound nitrogen atoms
    • C07D213/42—Radicals substituted by singly-bound nitrogen atoms having hetero atoms attached to the substituent nitrogen atom
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A61P31/14—Antivirals for RNA viruses
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A61P31/14—Antivirals for RNA viruses
    • A61P31/18—Antivirals for RNA viruses for HIV
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D263/32—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Virology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Molecular Biology (AREA)
  • AIDS & HIV (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Medicines Containing Plant Substances (AREA)
  • Peptides Or Proteins (AREA)

Abstract

SE REFIERE A UN PROCESO QUE CONSISTE EN: A) PROVISION DE UN PRIMER REACTIVO EN LA FORMA DE UN LIQUIDO; B) PROVISION DE UN SEGUNDO REACTIVO EN LA FORMA DE UN LIQUIDO; C) PROVISION DE UN TERCER REACTIVO PREMEZCLADO CON EL PRIMER O SEGUNDO REACTIVO; D) ADICION DE SEMILLAS AL PRIMER REACTIVO; E) REACCION DEL PRIMER REACTIVO CON UNA PRIMERA PORCION DEL SEGUNDO REACTIVO, EN UNA CANTIDAD PARA REACCIONAR CON MENOS DE APROXIMADAMENTE 15% EN PESO DEL PRIMER REACTIVO; F) HACER REACCIONAR EL PRIMER REACTIVO CON PORCIONES CADA VEZ MAYORES DEL SEGUNDO REACTIVO, MEDIANTE LA ADICION DEL SEGUNDO REACTIVO EN ETAPAS MULTIPLES O A UNA VELOCIDAD CONTINUAMENTE VARIADA PARA FORMAR CRISTALES DE LA SAL DEL PRODUCTO FARMACEUTICO. UN EJEMPLO ES LA OBTENCION DE 1-[4-PIRIDIN-2-IL)FENIL]-5(S)-2,5-BIS{[N-(METOXICARBONIL)-L-TER-LEUCINIL]AMINO}-4-(S)-HIDROXI-6-FENIL-2-AZAHEXANO. DICHO PROCESO PRODUCE CRISTALES DEL PRODUCTO FARMACEUTICO QUE TIENEN PROPIEDADES FISICAS DESEADAS Y CONSISTENTES DONDE LOS CRISTALES OBTENIDOS SON MAS GRANDES, MAS DEFINIDOS, CON UNA ESTRECHA DISTRIBUCION DE TAMANO DE PARTICULA Y MENOR CANTIDAD DE POLVOS FINOS
PE2005000498A 2004-05-04 2005-05-04 Proceso que emplea cristalizacion controlada en la formacion de cristales de un producto farmaceutico PE20060216A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US56804304P 2004-05-04 2004-05-04
US60753304P 2004-09-07 2004-09-07

Publications (1)

Publication Number Publication Date
PE20060216A1 true PE20060216A1 (es) 2006-03-17

Family

ID=35320785

Family Applications (2)

Application Number Title Priority Date Filing Date
PE2005000498A PE20060216A1 (es) 2004-05-04 2005-05-04 Proceso que emplea cristalizacion controlada en la formacion de cristales de un producto farmaceutico
PE2005000500A PE20060466A1 (es) 2004-05-04 2005-05-04 Proceso para preparar bisulfato de atazanavir y formas cristalinas del mismo

Family Applications After (1)

Application Number Title Priority Date Filing Date
PE2005000500A PE20060466A1 (es) 2004-05-04 2005-05-04 Proceso para preparar bisulfato de atazanavir y formas cristalinas del mismo

Country Status (8)

Country Link
US (1) US20050256314A1 (es)
EP (1) EP1758664A4 (es)
AR (2) AR049268A1 (es)
CL (1) CL2011003144A1 (es)
PE (2) PE20060216A1 (es)
RU (1) RU2385325C2 (es)
TW (3) TWI445697B (es)
WO (1) WO2005108380A2 (es)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TW200534879A (en) * 2004-03-25 2005-11-01 Bristol Myers Squibb Co Coated tablet formulation and method
US7829720B2 (en) * 2004-05-04 2010-11-09 Bristol-Myers Squibb Company Process for preparing atazanavir bisulfate and novel forms
TWI415635B (zh) * 2004-05-28 2013-11-21 必治妥施貴寶公司 加衣錠片調製物及製備彼之方法
DK2032521T3 (da) * 2006-06-27 2010-01-25 Sandoz Ag Ny fremgangsmåde til saltfremstilling
EP2178511B1 (en) * 2007-06-22 2011-03-02 Bristol-Myers Squibb Company Tableted compositions containing atazanavir
MX2009013461A (es) * 2007-06-22 2010-01-15 Bristol Myers Squibb Co Composiciones comprimidas que contienen atazanavir.
CN101778625A (zh) * 2007-06-22 2010-07-14 百时美施贵宝公司 含有阿扎那韦的压片组合物
EP2179272B1 (de) * 2007-07-10 2011-03-23 Boehringer Ingelheim International GmbH Optische befuellungskontrolle von pharmazeutischen kapseln auf kapselfuellmaschinen
WO2009014676A1 (en) * 2007-07-23 2009-01-29 Merck & Co., Inc. Novel crystalline form of a dihydrochloride salt of a dipeptidyl peptidase-iv inhibitor
EP2272830A1 (en) 2009-06-18 2011-01-12 Esteve Química, S.A. Preparation process of an antivirally heterocyclic azahexane derivative
CN104163787A (zh) * 2014-08-08 2014-11-26 山东威智医药工业有限公司 阿扎那韦及其硫酸盐的制备方法

Family Cites Families (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2940998A (en) * 1953-10-15 1960-06-14 Ajinomoto Kk Process for resolution of racemic glutamic acid and salts thereof
US4026897A (en) * 1974-01-31 1977-05-31 Otsuka Pharmaceutical Company 5-[1-Hydroxy-2-(substituted-amino)]alkyl-8-hydroxycarbostyril derivatives
DE3403329A1 (de) * 1984-02-01 1985-08-01 Horst Dr. 4019 Monheim Zerbe Pharmazeutisches produkt in form von pellets mit kontinuierlicher, verzoegerter wirkstoffabgabe
FR2623810B2 (fr) * 1987-02-17 1992-01-24 Sanofi Sa Sels de l'alpha-(tetrahydro-4,5,6,7 thieno(3,2-c) pyridyl-5) (chloro-2 phenyl) -acetate de methyle dextrogyre et compositions pharmaceutiques en contenant
US5158777A (en) * 1990-02-16 1992-10-27 E. R. Squibb & Sons, Inc. Captopril formulation providing increased duration of activity
CA2068402C (en) * 1991-06-14 1998-09-22 Michael R. Hoy Taste mask coatings for preparation of chewable pharmaceutical tablets
US5428048A (en) * 1993-11-08 1995-06-27 American Home Products Corporation Aryl-N-hydroxyureas as inhibitors of 5-lipoxygenase and anto-arteriosclerotic agents
GB9407386D0 (en) * 1994-04-14 1994-06-08 Smithkline Beecham Plc Pharmaceutical formulation
TW483763B (en) * 1994-09-02 2002-04-21 Astra Ab Pharmaceutical composition comprising of ramipril and dihydropyridine compound
US5849911A (en) * 1996-04-22 1998-12-15 Novartis Finance Corporation Antivirally active heterocyclic azahexane derivatives
US6087383A (en) * 1998-01-20 2000-07-11 Bristol-Myers Squibb Company Bisulfate salt of HIV protease inhibitor
KR20020015030A (ko) * 1999-03-22 2002-02-27 스티븐 비. 데이비스 ｃＧＭＰ 포스포디에스테라제의 접합된 피리도피리다진억제제
US6414002B1 (en) * 1999-09-22 2002-07-02 Bristol-Myers Squibb Company Substituted acid derivatives useful as antidiabetic and antiobesity agents and method
US6254888B1 (en) * 2000-01-28 2001-07-03 Boehringer Ingelheim Pharmaceuticals, Inc. Method for coating pharmaceutical dosage forms
US6395767B2 (en) * 2000-03-10 2002-05-28 Bristol-Myers Squibb Company Cyclopropyl-fused pyrrolidine-based inhibitors of dipeptidyl peptidase IV and method
CZ20011726A3 (cs) * 2000-05-26 2002-02-13 Pfizer Products Inc. Způsob reakční krystalizace, který umoľňuje řídit velikost částic
IL145106A0 (en) * 2000-08-30 2002-06-30 Pfizer Prod Inc Intermittent administration of a geowth hormone secretagogue
US6670344B2 (en) * 2000-09-14 2003-12-30 Bristol-Myers Squibb Company Combretastatin A-4 phosphate prodrug mono- and di-organic amine salts, mono- and di- amino acid salts, and mono- and di-amino acid ester salts
TW200534879A (en) * 2004-03-25 2005-11-01 Bristol Myers Squibb Co Coated tablet formulation and method
US7829720B2 (en) * 2004-05-04 2010-11-09 Bristol-Myers Squibb Company Process for preparing atazanavir bisulfate and novel forms
US20050288343A1 (en) * 2004-05-19 2005-12-29 Andrew Rusowicz Process of preparing substituted carbamates and intermediates thereof
TWI415635B (zh) * 2004-05-28 2013-11-21 必治妥施貴寶公司 加衣錠片調製物及製備彼之方法

Also Published As

Publication number Publication date
WO2005108380A2 (en) 2005-11-17
TW200606142A (en) 2006-02-16
RU2385325C2 (ru) 2010-03-27
AR049268A1 (es) 2006-07-12
CL2011003144A1 (es) 2012-04-13
AR048937A1 (es) 2006-06-14
EP1758664A4 (en) 2010-12-22
WO2005108380A3 (en) 2006-08-24
US20050256314A1 (en) 2005-11-17
EP1758664A2 (en) 2007-03-07
TWI518072B (zh) 2016-01-21
TW200600498A (en) 2006-01-01
RU2006142768A (ru) 2008-06-10
TW201427949A (zh) 2014-07-16
TWI445697B (zh) 2014-07-21
PE20060466A1 (es) 2006-06-01

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Legal Events

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