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AR133154A2 - Proceso de producción de cristales de derivado de diazabiciclooctano y preparación liofilizada estable - Google Patents

Proceso de producción de cristales de derivado de diazabiciclooctano y preparación liofilizada estable

Info

Publication number
AR133154A2
AR133154A2 ARP240101721A ARP240101721A AR133154A2 AR 133154 A2 AR133154 A2 AR 133154A2 AR P240101721 A ARP240101721 A AR P240101721A AR P240101721 A ARP240101721 A AR P240101721A AR 133154 A2 AR133154 A2 AR 133154A2
Authority
AR
Argentina
Prior art keywords
compound
crystals
lyophilized composition
formula
aqueous solution
Prior art date
Application number
ARP240101721A
Other languages
English (en)
Inventor
Takaya Ogawa
Takuya Yokoyama
Shusuke Furuyama
Masato Ichiki
Kenichi Fushihara
Original Assignee
Meiji Seika Pharma Co Ltd
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 Meiji Seika Pharma Co Ltd filed Critical Meiji Seika Pharma Co Ltd
Publication of AR133154A2 publication Critical patent/AR133154A2/es

Links

Classifications

    • 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
    • A61K31/439Heterocyclic 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 the ring forming part of a bridged ring system, e.g. quinuclidine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/02Inorganic compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0012Galenical forms characterised by the site of application
    • A61K9/0019Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/14Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/19Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles lyophilised, i.e. freeze-dried, solutions or dispersions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/08Bridged systems
    • 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)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Organic Chemistry (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Dermatology (AREA)
  • Inorganic Chemistry (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicinal Preparation (AREA)

Abstract

Los objetos de la presente invención consisten en proporcionar un proceso para producir cristales del compuesto (1) con facilidad en una escala industrial y una composición liofilizada estable de compuesto (1). Se halló que sometiendo una solución acuosa que contiene el compuesto (1) y una sal inorgánica tal como cloruro de sodio a liofilización da como resultado una composición liofilizada con buena estabilidad de almacenamiento, en donde el compuesto (1) es cristalino y también que los cristales del compuesto (1) se pueden obtener de dicha solución acuosa sin liofilización. Reivindicación 1: Un proceso para producir cristales de un compuesto representado por la fórmula (1) caracterizado porque comprende la cristalización del compuesto en una solución acuosa que contiene el compuesto y una sal inorgánica. Reivindicación 7: Un proceso para producir una composición liofilizada caracterizado porque comprende un compuesto representado por la fórmula (1) que comprende la cristalización del compuesto por el proceso de acuerdo con la reivindicación 1. Reivindicación 8: Un proceso para producir una composición liofilizada caracterizado porque comprende un compuesto representado por la fórmula (1) que comprende la cristalización del compuesto sometiendo una solución acuosa que contiene el compuesto y una sal inorgánica a liofilización. Reivindicación 13: Una composición liofilizada, caracterizada porque comprende cristales de un compuesto representado por la fórmula (1) y una sal inorgánica.
ARP240101721A 2014-12-05 2024-07-02 Proceso de producción de cristales de derivado de diazabiciclooctano y preparación liofilizada estable AR133154A2 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2014246425 2014-12-05

Publications (1)

Publication Number Publication Date
AR133154A2 true AR133154A2 (es) 2025-09-03

Family

ID=56091802

Family Applications (2)

Application Number Title Priority Date Filing Date
ARP150103970A AR102915A1 (es) 2014-12-05 2015-12-04 Proceso de producción de cristales de derivado de diazabiciclooctano y preparación liofilizada estable
ARP240101721A AR133154A2 (es) 2014-12-05 2024-07-02 Proceso de producción de cristales de derivado de diazabiciclooctano y preparación liofilizada estable

Family Applications Before (1)

Application Number Title Priority Date Filing Date
ARP150103970A AR102915A1 (es) 2014-12-05 2015-12-04 Proceso de producción de cristales de derivado de diazabiciclooctano y preparación liofilizada estable

Country Status (18)

Country Link
US (2) US10294224B2 (es)
EP (1) EP3228620B1 (es)
JP (1) JP6779787B2 (es)
KR (1) KR102555657B1 (es)
CN (1) CN107001366B (es)
AR (2) AR102915A1 (es)
AU (1) AU2015355970B2 (es)
BR (1) BR112017010445B8 (es)
CA (1) CA2969192C (es)
ES (1) ES2821826T3 (es)
IL (1) IL252691B (es)
MX (1) MX2017007191A (es)
MY (1) MY190283A (es)
RU (1) RU2732129C2 (es)
SG (1) SG11201704576SA (es)
TW (1) TWI691499B (es)
WO (1) WO2016088863A1 (es)
ZA (1) ZA201704063B (es)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NZ701959A (en) 2012-05-30 2016-07-29 Meiji Seika Pharma Co Ltd Novel β-lactamase inhibitor and method for producing same
EP3067355B1 (en) 2013-10-08 2020-12-16 Meiji Seika Pharma Co., Ltd. Crystals of diazabicyclooctane derivative and production method for crystals of diazabicyclooctane derivative
SG11201704576SA (en) * 2014-12-05 2017-07-28 Meiji Seika Pharma Co Ltd Method for producing crystals of diazabicyclooctane derivative and stable lyophilized preparation
JP7179058B2 (ja) * 2017-09-27 2022-11-28 Meiji Seikaファルマ株式会社 ジアザビシクロオクタン誘導体の剤形およびその生産プロセス
EP3687993A1 (en) 2017-09-27 2020-08-05 Meiji Seika Pharma Co., Ltd. Pharmaceutical forms of diazabicyclooctane derivatives and manufacturing method thereof
KR20200091395A (ko) 2017-09-27 2020-07-30 페도라 파마슈티칼스 인코포레이티드 디아자비시클로옥탄 유도체의 결정형 및 그의 제조 방법
JP6375463B1 (ja) * 2018-02-28 2018-08-15 日本曹達株式会社 ビス(フルオロスルホニル)アミドアルカリ金属塩粉末の製造方法
CN110314163A (zh) * 2018-03-30 2019-10-11 杭州森泽医药科技有限公司 一种拉氧头孢钠药物组合物及应用
JP7638693B2 (ja) * 2020-12-15 2025-03-04 大阪瓦斯株式会社 ヒドロキシアルカン酸結晶の製造方法及びヒドロキシアルカン酸の結晶多形体

Family Cites Families (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6019759B2 (ja) 1977-11-24 1985-05-17 イ−ライ・リリ−・アンド・カンパニ− 非経口投予用11115152139199東京都中央区京橋2丁目3番13号
GB1589317A (en) * 1977-11-24 1981-05-13 Lilly Co Eli Freeze drying cephalothin sodium
JPS6019759A (ja) 1983-07-15 1985-01-31 Nippon Soda Co Ltd ホルムアミドオキシム誘導体その製造方法及び農園芸用殺菌剤
JPS60255723A (ja) 1984-05-31 1985-12-17 Ono Pharmaceut Co Ltd メシル酸ガベキサートの結晶性凍結乾燥製剤及びその製造方法
JPH07117533B2 (ja) 1985-08-28 1995-12-18 株式会社生体科学研究所 トランスフエリンおよびその用途
PL157979B1 (pl) 1989-02-14 1992-07-31 Sprezyna z dwoma stanami równowagi trwalej PL PL
US20030220521A1 (en) 1989-07-27 2003-11-27 G.D. Searle & Co. Renal-selective prodrugs for control of renal sympathetic nerve activity in the treatment of hypertension
TW264475B (es) 1991-09-20 1995-12-01 Takeda Pharm Industry Co Ltd
JP2843444B2 (ja) * 1994-05-02 1999-01-06 塩野義製薬株式会社 ピロリジルチオカルバペネム誘導体の結晶,該結晶を含む凍結乾燥製剤,およびその製造方法
ATE223916T1 (de) * 1994-05-02 2002-09-15 Shionogi & Co Kristalline pyrrolidylthiocarbapenem derivate, lyophilisierste präparationen dieser kristalle und verfahren zu deren herstellung
DE19531874C1 (de) 1995-08-30 1996-10-02 Daimler Benz Ag Seitenwandbaugruppe für eine Kraftfahrzeugkarosserie
TWI233805B (en) * 1999-07-01 2005-06-11 Fujisawa Pharmaceutical Co Stabilized pharmaceutical composition in lyophilized form as antifungal agent
FR2812635B1 (fr) 2000-08-01 2002-10-11 Aventis Pharma Sa Nouveaux composes heterocycliques, preparation et utilisation comme medicaments notamment comme anti- bacteriens
FR2825705B1 (fr) 2001-06-08 2005-05-20 Aventis Pharma Sa Nouveaux composes heterocycliques, leur preparation et leur utilisation comme medicaments, notamment comme anti-bacteriens
FR2835186B1 (fr) 2002-01-28 2006-10-20 Aventis Pharma Sa Nouveaux composes heterocycliques, actifs comme inhibiteurs de beta-lactamases
FR2921060B1 (fr) 2007-09-14 2012-06-15 Novexel Nouveau procede de preparation d'une piperidine disubsituee et nouveaux intermediaires
WO2009091856A2 (en) 2008-01-18 2009-07-23 Merck & Co., Inc. Beta-lactamase inhibitors
FR2930553B1 (fr) 2008-04-29 2010-05-21 Novexel Composes azabicycliques, leur preparation et leur utilisation comme medicaments, notamment inhibiteurs de beta-lactamases
FR2936798B1 (fr) 2008-10-03 2012-09-28 Novexel Nouveaux composes heterocycliques azotes, leur preparation et leur utilisation comme medicaments antibacteriens.
US20120053350A1 (en) 2009-04-30 2012-03-01 Ian Mangion Preparation of alkyl esters of n-protected oxo-azacycloalkylcarboxylic acids
FR2951171A1 (fr) 2009-10-09 2011-04-15 Novexel Nouveau sel de sodium d'un compose azabicyclique sous forme enantiomere cristallisee et nouvelles formes polymorphes et pseudopolymorphes ainsi que leur preparation
US8772490B2 (en) 2010-12-22 2014-07-08 Meiji Seika Pharma Co., Ltd. Optically active diazabicyclooctane derivatives and process for preparing the same
HUE032491T2 (en) 2010-12-22 2017-09-28 Meiji Seika Pharma Co Ltd An optically active diaza-bicyclooctane derivative and a process for its preparation
WO2012172368A1 (en) 2011-06-17 2012-12-20 Astrazeneca Ab Process for preparing heterocyclic compounds including trans-7-oxo-6-(sulphooxy)-1,6-diazabicyclo[3,2,1]octane-2-carboxamide and salts thereof
US8822450B2 (en) 2011-08-27 2014-09-02 Wockhardt Ltd. 1,6-diazabicyclo [3,2,1] octan-7-one derivatives and their use in the treatment of bacterial infections
KR101618424B1 (ko) 2011-08-30 2016-05-04 욱크하르트 리미티드 1,6-디아자비시클로[3,2,1]옥탄-7-온 유도체 및 세균 감염 치료에서의 그 유도체의 용도
CN103781787B (zh) 2011-09-13 2015-09-23 沃克哈特有限公司 含氮化合物及其用途
US8796257B2 (en) * 2011-12-02 2014-08-05 Naeja Pharmaceutical Inc. Bicyclic compounds and their use as antibacterial agents and β-lactamase inhibitors
US9505761B2 (en) 2011-12-02 2016-11-29 Fedora Pharmaceuticals Inc. Bicyclic compounds and their use as antibacterial agents and beta-lactamase inhibitors
NZ701959A (en) 2012-05-30 2016-07-29 Meiji Seika Pharma Co Ltd Novel β-lactamase inhibitor and method for producing same
NZ718009A (en) * 2013-09-24 2018-03-23 Meiji Seika Pharma Co Ltd Process for producing diazabicyclooctane derivative and intermediate thereof
EP3067355B1 (en) 2013-10-08 2020-12-16 Meiji Seika Pharma Co., Ltd. Crystals of diazabicyclooctane derivative and production method for crystals of diazabicyclooctane derivative
SG11201704576SA (en) 2014-12-05 2017-07-28 Meiji Seika Pharma Co Ltd Method for producing crystals of diazabicyclooctane derivative and stable lyophilized preparation

Also Published As

Publication number Publication date
AU2015355970B2 (en) 2020-05-21
ES2821826T3 (es) 2021-04-27
TWI691499B (zh) 2020-04-21
US20190202831A1 (en) 2019-07-04
CA2969192A1 (en) 2016-06-09
IL252691A0 (en) 2017-08-31
ZA201704063B (en) 2021-10-27
EP3228620A4 (en) 2018-05-02
US10294224B2 (en) 2019-05-21
EP3228620B1 (en) 2020-09-02
RU2017123112A (ru) 2019-01-09
TW201629062A (zh) 2016-08-16
BR112017010445A2 (pt) 2017-12-26
JPWO2016088863A1 (ja) 2017-09-14
EP3228620A1 (en) 2017-10-11
IL252691B (en) 2020-08-31
SG11201704576SA (en) 2017-07-28
JP6779787B2 (ja) 2020-11-04
CN107001366A (zh) 2017-08-01
MX2017007191A (es) 2017-08-28
WO2016088863A1 (ja) 2016-06-09
NZ732214A (en) 2021-10-29
BR112017010445B1 (pt) 2024-01-30
MY190283A (en) 2022-04-12
CA2969192C (en) 2023-02-28
US11117895B2 (en) 2021-09-14
RU2732129C2 (ru) 2020-09-11
KR102555657B1 (ko) 2023-07-18
US20170327499A1 (en) 2017-11-16
AU2015355970A1 (en) 2017-06-15
RU2017123112A3 (es) 2019-06-25
KR20170094272A (ko) 2017-08-17
CN107001366B (zh) 2020-08-28
BR112017010445B8 (pt) 2024-02-27
AR102915A1 (es) 2017-04-05

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