[go: up one dir, main page]

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)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • General Chemical & Material Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Veterinary Medicine (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)
  • Peptides Or Proteins (AREA)
  • Medicines Containing Plant Substances (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) AR048937A1 (es)
CL (1) CL2011003144A1 (es)
PE (2) PE20060216A1 (es)
RU (1) RU2385325C2 (es)
TW (3) TWI518072B (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
TWI354569B (en) * 2004-05-28 2011-12-21 Bristol Myers Squibb Co Coated tablet formulation and method
EP2436381A1 (en) * 2006-06-27 2012-04-04 Sandoz AG Crystallization of hydrohalides of pharmaceutical compounds
SI2178513T1 (sl) * 2007-06-22 2011-05-31 Bristol Myers Squibb Co Tabletni sestavki vsebujoäśi atazanavir
ES2359770T3 (es) * 2007-06-22 2011-05-26 Bristol-Myers Squibb Company Composiciones en comprimidos que contienen atazanavir.
US20100178339A1 (en) * 2007-06-22 2010-07-15 Bristol-Myers Squibb Company Tableted compositions containing atazanavir
CN101688844B (zh) * 2007-07-10 2013-02-27 贝林格尔.英格海姆国际有限公司 胶囊填充机中药物胶囊的光学填充控制
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
CN1161341C (zh) * 1999-03-22 2004-08-11 布里斯托尔-迈尔斯斯奎布公司 cGMP磷酸二酯酶的稠合吡啶并哒嗪抑制剂
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
TWI354569B (en) * 2004-05-28 2011-12-21 Bristol Myers Squibb Co Coated tablet formulation and method

Also Published As

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

Similar Documents

Publication Publication Date Title
Wheeler et al. Not just going with the flow: the effects of fluid flow on bacteria and plankton
Smart et al. The emerging role of TYRO3 as a therapeutic target in cancer
PE20060216A1 (es) Proceso que emplea cristalizacion controlada en la formacion de cristales de un producto farmaceutico
Drori et al. A supramolecular ice growth inhibitor
Glennon Bath salts, mephedrone, and methylenedioxypyrovalerone as emerging illicit drugs that will need targeted therapeutic intervention
Moritz et al. The newest achievements in synthesis, immobilization and practical applications of antibacterial nanoparticles
Huang et al. Biomimetic peptoid oligomers as dual-action antifreeze agents
Tian et al. Bioinspired cryoprotectants enabled by binary natural deep eutectic solvents for sustainable and green cryopreservation
Sheetz A tale of two states: normal and transformed, with and without rigidity sensing
CY1117326T1 (el) Παραγωγο κατεχολαμινης χρησιμο για τη θεραπεια ασθενειας parkinson
EP4338803A3 (en) Process for the preparation of erythrocytes loaded with one or more substances of pharmaceutical interest and so obtained erythrocytes
CY1109142T1 (el) Χαρακτηρισμος: σπειροκυκλικα παραγωγα κυκλοεξανιου
CY1110913T1 (el) Παραγωγα 2-πυρρολιδιν-2-υλο-[1,3,4]-οξαδιαζολης και η χρησιμοποιηση τους σαν αντικαταθλιπτικα
Cui et al. Hyperactive antifreeze proteins promote ice growth before binding to it
Duerschmied et al. The role of serotonin in haemostasis
Thatoi et al. Prebiotics and their production from unconventional raw materials (Mushrooms)
Benish et al. Surgery as a double-edged sword: a clinically feasible approach to overcome the metastasis-promoting effects of surgery by blunting stress and prostaglandin responses
DE602004002584D1 (de) Verwendung von 7-nitro-2,1,3-benzoxadiazol derivaten zur behandlung von krebserkrankungen
Rzepinski et al. Kosmotropic behavior of 3-pyrroline during crystalline hydrates formation
Potkin et al. The influence of heterocyclic compound-PAMAM dendrimer complexes on evoked electrical responses in slices of hypoxic brain tissue
Mirzaaghaei et al. Ferula gummosa Boiss flower and leaf extracts inhibit angiogenesis in vitro
Banerjee et al. Thermodynamics and spectroscopic properties of C2H5CONH2 found in Sagittarius B2 (N1)
Ahmad et al. Astudy of population dynamics of normal and immune cells in presence of tumor cells
Kscheschinski et al. Calcium regulates cortex contraction in Physarum polycephalum
Glitsch Extracellular acidosis and cancer

Legal Events

Date Code Title Description
FD Application declared void or lapsed