MX2017002790A - Sal de un derivado de cefalosporina, forma solida cristalina del mismo y metodo para su produccion. - Google Patents

Sal de un derivado de cefalosporina, forma solida cristalina del mismo y metodo para su produccion.

Info

Publication number
MX2017002790A
MX2017002790A MX2017002790A MX2017002790A MX2017002790A MX 2017002790 A MX2017002790 A MX 2017002790A MX 2017002790 A MX2017002790 A MX 2017002790A MX 2017002790 A MX2017002790 A MX 2017002790A MX 2017002790 A MX2017002790 A MX 2017002790A
Authority
MX
Mexico
Prior art keywords
salt
same
solid form
crystalline solid
cephalosporin derivative
Prior art date
Application number
MX2017002790A
Other languages
English (en)
Inventor
Matsubara Fumihiko
Kurita Takanori
Nagamatsu Daiki
Original Assignee
Shionogi & 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
Application filed by Shionogi & Co filed Critical Shionogi & Co
Publication of MX2017002790A publication Critical patent/MX2017002790A/es

Links

Classifications

    • 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
    • A61K31/54—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
    • A61K31/542—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/545—Compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins, cefaclor, or cephalexine
    • A61K31/546—Compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins, cefaclor, or cephalexine containing further heterocyclic rings, e.g. cephalothin
    • 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
    • A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/02—Inorganic compounds
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/19—Particulate 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
    • 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
    • A61P31/04—Antibacterial agents
    • 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
    • A61P31/10—Antimycotics
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D227/00—Heterocyclic compounds containing rings having one nitrogen atom as the only ring hetero atom, according to more than one of groups C07D203/00 - C07D225/00
    • C07D227/02—Heterocyclic compounds containing rings having one nitrogen atom as the only ring hetero atom, according to more than one of groups C07D203/00 - C07D225/00 with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D227/06—Heterocyclic compounds containing rings having one nitrogen atom as the only ring hetero atom, according to more than one of groups C07D203/00 - C07D225/00 with 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D501/00—Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
    • C07D501/14—Compounds having a nitrogen atom directly attached in position 7
    • C07D501/16—Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D501/00—Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
    • C07D501/14—Compounds having a nitrogen atom directly attached in position 7
    • C07D501/16—Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
    • C07D501/20—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids
    • C07D501/24—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids with hydrocarbon radicals, substituted by hetero atoms or hetero rings, attached in position 3
    • C07D501/38—Methylene radicals, substituted by nitrogen atoms; Lactams thereof with the 2-carboxyl group; Methylene radicals substituted by nitrogen-containing hetero rings attached by the ring nitrogen atom; Quaternary compounds thereof
    • C07D501/46—Methylene radicals, substituted by nitrogen atoms; Lactams thereof with the 2-carboxyl group; Methylene radicals substituted by nitrogen-containing hetero rings attached by the ring nitrogen atom; Quaternary compounds thereof with the 7-amino radical acylated by carboxylic acids containing hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/80—Process related aspects concerning the preparation of the cosmetic composition or the storage or application thereof
    • A61K2800/84—Products or compounds obtained by lyophilisation, freeze-drying

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Epidemiology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Inorganic Chemistry (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Cephalosporin Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

La presente invención proporciona una sal de adición ácida o una sal de sodio de un compuesto representado por la fórmula (IA), o su hidrato de la sal o una forma sólida cristalina estable de la sal. La sal o la forma sólida cristalina de la misma, es extremadamente útil como un ingrediente activo para la producción de un producto farmacéutico.
MX2017002790A 2014-09-04 2015-09-03 Sal de un derivado de cefalosporina, forma solida cristalina del mismo y metodo para su produccion. MX2017002790A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2014179853 2014-09-04
PCT/JP2015/075039 WO2016035845A1 (ja) 2014-09-04 2015-09-03 セファロスポリン誘導体の塩、その結晶性固体およびその製造方法

Publications (1)

Publication Number Publication Date
MX2017002790A true MX2017002790A (es) 2017-05-30

Family

ID=55439902

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2017002790A MX2017002790A (es) 2014-09-04 2015-09-03 Sal de un derivado de cefalosporina, forma solida cristalina del mismo y metodo para su produccion.

Country Status (25)

Country Link
US (1) US10004750B2 (es)
EP (1) EP3190115B1 (es)
JP (1) JP6120429B2 (es)
KR (2) KR20170043663A (es)
CN (1) CN106795176B (es)
AU (1) AU2015312828B2 (es)
BR (1) BR112017004166B1 (es)
CA (1) CA2959295C (es)
CY (1) CY1124838T1 (es)
DK (1) DK3190115T3 (es)
EA (1) EA035845B1 (es)
ES (1) ES2893424T3 (es)
HR (1) HRP20211524T1 (es)
HU (1) HUE056038T2 (es)
LT (1) LT3190115T (es)
MA (1) MA40585A (es)
MX (1) MX2017002790A (es)
MY (1) MY178017A (es)
PH (1) PH12017500435A1 (es)
PL (1) PL3190115T3 (es)
PT (1) PT3190115T (es)
RS (1) RS62449B1 (es)
SI (1) SI3190115T1 (es)
TW (1) TWI593690B (es)
WO (1) WO2016035845A1 (es)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2017216765A1 (en) * 2016-06-17 2017-12-21 Wockhardt Limited Antibacterial compositions
WO2020184399A1 (ja) * 2019-03-08 2020-09-17 塩野義製薬株式会社 抗菌用医薬組成物
TW202220663A (zh) 2020-07-28 2022-06-01 日商鹽野義製藥股份有限公司 含有具有鄰苯二酚基之頭孢菌素類的凍結乾燥製劑及其製造方法

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2009310959B2 (en) * 2008-10-31 2015-05-07 Shionogi & Co., Ltd. Cephalosporin having catechol group
MX2012011521A (es) * 2010-04-05 2013-03-08 Shionogi & Co Compuestos cefem que tienen un grupo catecol.
UY35103A (es) * 2012-10-29 2014-05-30 Glaxo Group Ltd Compuestos de cefem 2-sustituidos
KR101935186B1 (ko) * 2014-09-04 2019-01-03 시오노기세야쿠 가부시키가이샤 카테콜기를 갖는 세팔로스포린류를 함유하는 제제

Also Published As

Publication number Publication date
ES2893424T3 (es) 2022-02-09
AU2015312828B2 (en) 2020-02-13
DK3190115T3 (da) 2021-10-25
CN106795176B (zh) 2020-11-10
TWI593690B (zh) 2017-08-01
KR20180088750A (ko) 2018-08-06
EP3190115B1 (en) 2021-08-25
CN106795176A (zh) 2017-05-31
WO2016035845A1 (ja) 2016-03-10
LT3190115T (lt) 2021-12-10
CA2959295C (en) 2023-08-22
JP6120429B2 (ja) 2017-04-26
AU2015312828A1 (en) 2017-03-16
MA40585A (fr) 2021-04-14
PL3190115T3 (pl) 2021-12-27
EP3190115A4 (en) 2018-02-21
HRP20211524T1 (hr) 2021-12-24
KR102284990B1 (ko) 2021-08-04
CY1124838T1 (el) 2022-11-25
HUE056038T2 (hu) 2022-01-28
MY178017A (en) 2020-09-29
TW201609753A (zh) 2016-03-16
EP3190115A1 (en) 2017-07-12
PT3190115T (pt) 2021-10-19
PH12017500435A1 (en) 2017-07-31
EA201790522A1 (ru) 2017-07-31
US20170281638A1 (en) 2017-10-05
BR112017004166A2 (pt) 2017-12-05
US10004750B2 (en) 2018-06-26
CA2959295A1 (en) 2016-03-10
SI3190115T1 (sl) 2021-11-30
RS62449B1 (sr) 2021-11-30
JPWO2016035845A1 (ja) 2017-05-25
BR112017004166B1 (pt) 2022-11-29
EA035845B1 (ru) 2020-08-19
KR20170043663A (ko) 2017-04-21

Similar Documents

Publication Publication Date Title
PH12020551089A1 (en) Pyrrolopyrimidine compounds used as tlr7 agonist
JOP20200225A1 (ar) مشتق كوينولين عالي النقاء وطريقة لإنتاجه
NZ729037A (en) Carboxylic acid compound, method for preparation thereof, and use thereof
MX2015011913A (es) Moduladores de acido oxabiciclo[2.2.2] gpr120.
MX2013005241A (es) Cristal de derivado de 6,7-insaturado-7-carbamoil morfinano y metodo para producir el mismo.
PH12018501644A1 (en) Tlr7 agonist maleate salt, crystalline forms c, d and e thereof, preparation methods and uses of maleate salt and crystalline forms
PH12016501517A1 (en) Tetrazolone-substituted dihydropyridinone mgat2 inhibitors
PH12014501711A1 (en) Benzyl sulfonamide derivatives useful as mogat-2 inhibitors
MY190283A (en) Method for producing crystals of diazabicyclooctane derivative and stable lyophilized preparation
CY1124838T1 (el) Αλας παραγωγου κεφαλοσπορινης, κρυσταλλικη, στερεη μορφη αυτου και μεθοδος παραγωγης αυτου
MY185367A (en) Improved process for the preparation of osimertinib (azd9291) or a salt thereof, and ?azd9291 aniline? or a salt thereof
MX2019001228A (es) Metodo de produccion del compuesto de pirazol-amida.
WO2016142819A3 (en) Novel process for the preparation of ranolazine
MX2017008074A (es) DERIVADOS DE IMIDAZOPIRIDAZINA COMO INHIBIDORES DE FOSFOINOSITIDA-3-QUINASAS BETA (PI3Kß).
PH12017501404A1 (en) Diaza-benzofluoranthrene compounds
AU2015280874A1 (en) Novel heterocyclic compound
EP4282973A3 (en) Processes for the preparation of pyrimidinylcyclopentane compounds
WO2015191681A3 (en) Substituted pyridinones as mgat2 inhibitors
TW201613944A (en) Crystal of cyclic phosphonic acid sodium salt and method for manufacturing same
MX2017008076A (es) DERIVADOS DE IMIDAZOPIRIDAZINA ENLAZADOS A HETEROCICLILO COMO INHIBIDORES DE PI3Kß.
IN2014MU00071A (es)
TH170794B (th) เกลือของอนุพันธ์เซฟาโลสปอริน, ของแข็งคริสตัลไลน์ของมัน และวิธีของการผลิตของมัน
TN2014000308A1 (en) Benzyl sulfonamide derivatives useful as mogat - 2 inhibitors

Legal Events

Date Code Title Description
FG Grant or registration