MA46266B1 - Formes cristallines - Google Patents

Formes cristallines

Info

Publication number
MA46266B1
MA46266B1 MA46266A MA46266A MA46266B1 MA 46266 B1 MA46266 B1 MA 46266B1 MA 46266 A MA46266 A MA 46266A MA 46266 A MA46266 A MA 46266A MA 46266 B1 MA46266 B1 MA 46266B1
Authority
MA
Morocco
Prior art keywords
crystalline forms
crystal forms
pharmaceutical compositions
phosphono
pyrrolidin
Prior art date
Application number
MA46266A
Other languages
English (en)
Other versions
MA46266A (fr
Inventor
Raumer Markus Von
Daniel Leuenberger
Stefan Reber
Original Assignee
Idorsia Pharmaceuticals 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 Idorsia Pharmaceuticals Ltd filed Critical Idorsia Pharmaceuticals Ltd
Publication of MA46266A publication Critical patent/MA46266A/fr
Publication of MA46266B1 publication Critical patent/MA46266B1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6558—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system
    • C07F9/65583—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system each of the hetero rings containing nitrogen as ring hetero atom
    • 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
    • A61K31/66—Phosphorus compounds
    • A61K31/675—Phosphorus compounds having nitrogen as a ring hetero atom, e.g. pyridoxal phosphate
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00—Drugs for disorders of the senses
    • A61P27/02—Ophthalmic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00—Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13—Crystalline forms, e.g. polymorphs

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Biochemistry (AREA)
  • Molecular Biology (AREA)
  • Urology & Nephrology (AREA)
  • Vascular Medicine (AREA)
  • Epidemiology (AREA)
  • Ophthalmology & Optometry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

L'invention concerne des formes cristallines de chlorhydrate d'ester butylique 4- ( r )-2-{[6- (( s )-3-méthoxy-pyrrolidin-1-yl)-2-phényl-pyrimidine-4-carbonyl]-amino}-3-phosphono-propionyl)-pipérazine-1-carboxylique, des procédés pour leur préparation, des compositions pharmaceutiques comprenant lesdites formes cristallines, des compositions pharmaceutiques préparées à partir de telles formes cristallines et leur utilisation en tant que médicament, en particulier en tant qu'antagoniste du récepteur p2y 12 .
MA46266A 2016-09-22 2017-09-21 Formes cristallines MA46266B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP2016072562 2016-09-22
PCT/EP2017/073858 WO2018055016A1 (fr) 2016-09-22 2017-09-21 Formes cristallines

Publications (2)

Publication Number Publication Date
MA46266A MA46266A (fr) 2019-07-31
MA46266B1 true MA46266B1 (fr) 2022-02-28

Family

ID=59923448

Family Applications (1)

Application Number Title Priority Date Filing Date
MA46266A MA46266B1 (fr) 2016-09-22 2017-09-21 Formes cristallines

Country Status (27)

Country Link
US (4) US10730896B2 (fr)
EP (2) EP3981774A1 (fr)
JP (1) JP7097369B2 (fr)
KR (1) KR102552795B1 (fr)
CN (1) CN109715639B (fr)
AU (1) AU2017331930B2 (fr)
CA (1) CA3037794A1 (fr)
CL (1) CL2019000728A1 (fr)
CY (1) CY1125052T1 (fr)
DK (1) DK3515924T3 (fr)
EA (1) EA201990723A1 (fr)
ES (1) ES2908572T3 (fr)
HR (1) HRP20220234T1 (fr)
HU (1) HUE057772T2 (fr)
IL (1) IL265445B2 (fr)
LT (1) LT3515924T (fr)
MA (1) MA46266B1 (fr)
MX (1) MX381590B (fr)
MY (1) MY193080A (fr)
PH (1) PH12019500567B1 (fr)
PL (1) PL3515924T3 (fr)
PT (1) PT3515924T (fr)
RS (1) RS62946B1 (fr)
SI (1) SI3515924T1 (fr)
TW (1) TWI752086B (fr)
UA (1) UA124073C2 (fr)
WO (1) WO2018055016A1 (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
HUE057772T2 (hu) 2016-09-22 2022-06-28 Idorsia Pharmaceuticals Ltd Kristályos formák
US11179390B2 (en) 2017-03-15 2021-11-23 Idorsia Pharmaceuticals Ltd Subcutaneous administration of a P2Y12 receptor antagonist
DK4181872T3 (da) 2020-07-15 2026-01-26 Viatris Asia Pacific Pte Ltd Vandig, farmaceutisk sammensætning omfattende en p2y12 receptorantagonist
MX2024000653A (es) * 2021-07-13 2024-01-31 Idorsia Pharmaceuticals Ltd Un proceso para la sintesis de ester de butilo de acido 4-((r)-2-{[6-((s)-3-metoxi-pirrolidin-1-il)-2-fenil-pirimidin-4-c arbonil]-amino}-3-fosfono-propionil)-piperazin-1-carboxilico.

Family Cites Families (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5373586A (en) 1976-12-09 1978-06-30 Mitsubishi Chem Ind Ltd New penicillin derivatives
CA2020437A1 (fr) 1989-07-05 1991-01-06 Yoshihide Fuse Derive de cinnamamide
US6855715B1 (en) 1999-06-14 2005-02-15 Eli Lilly And Company Serine protease inhibitors
US6861424B2 (en) 2001-06-06 2005-03-01 Schering Aktiengesellschaft Platelet adenosine diphosphate receptor antagonists
CA2507657C (fr) 2002-12-11 2011-05-31 Bayer Schering Pharma Aktiengesellschaft Composes de 2-aminocarbonyl-quinoline utilises en tant qu'antagonistes du recepteur de l'adenosine diphosphate des plaquettes
PT1611144E (pt) 2003-04-09 2010-11-12 Wyeth Llc Derivados do ácido 2-(8,9-dioxo-2,6-diazabiciclo(5.2.0)- non-1(7)-eno-2-il)-alquil-fosfónico e sua utilização como antagonistas do receptor n-metil-d-aspartato (nmda)
TW200640877A (en) 2005-04-28 2006-12-01 Actelion Pharmaceuticals Ltd Pyrimidine derivatives
ES2421448T3 (es) 2005-10-21 2013-09-02 Actelion Pharmaceuticals Ltd Derivados de piperazina como agentes contra la malaria
CL2007002920A1 (es) 2006-10-13 2008-06-06 Actelion Pharmaceuticals Ltd Compuestos derivados de 2-aminocarbonilpiridina; composicion farmaceutica; y uso para el tratamiento de trastornos vasculares oclusivos.
CL2007003038A1 (es) 2006-10-25 2008-06-06 Actelion Pharmaceuticals Ltd Compuestos derivados de 2-fenil-6-aminocarbonil-pirimidina; composicion farmaceutica; y uso en el tratamiento de trastornos vasculares oclusivos.
JP4785881B2 (ja) 2007-02-27 2011-10-05 大塚製薬株式会社 医薬
CA2684644A1 (fr) 2007-04-23 2008-10-30 Sanofi-Aventis Derives de quinoleine-carboxamide comme antagonistes de p2y12
BRPI0819696B1 (pt) 2007-11-29 2018-10-23 Actelion Pharmaceuticals Ltd compostos de derivados de 2-fenil-pirimidina, composição farmacêutica e uso de um composto
JP5504171B2 (ja) 2007-12-26 2014-05-28 サノフイ P2y12アンタゴニストとしてのヘテロサイクリックピラゾール−カルボキサミド
JP5560202B2 (ja) 2007-12-26 2014-07-23 サノフイ P2y12拮抗薬としてのピラゾール−カルボキサミド誘導体
AR071653A1 (es) 2008-04-11 2010-07-07 Actelion Pharmaceuticals Ltd Derivados 2-fenil-4-ciclopropil-pirimidina
AR071652A1 (es) 2008-04-11 2010-07-07 Actelion Pharmaceuticals Ltd Derivados 2- fenil-piridina substituidos
WO2010116328A2 (fr) 2009-04-08 2010-10-14 Actelion Pharmaceuticals Ltd 6-(3-azabicyclo[3.1.0]hex-3-yl)-2-phénylpyrimidines
KR101728180B1 (ko) 2009-04-22 2017-04-18 액테리온 파마슈티칼 리미티드 티아졸 유도체들 및 p2y12 수용체 길항제로서 이들의 용도
HUE057772T2 (hu) 2016-09-22 2022-06-28 Idorsia Pharmaceuticals Ltd Kristályos formák
US11179390B2 (en) 2017-03-15 2021-11-23 Idorsia Pharmaceuticals Ltd Subcutaneous administration of a P2Y12 receptor antagonist
DK4181872T3 (da) 2020-07-15 2026-01-26 Viatris Asia Pacific Pte Ltd Vandig, farmaceutisk sammensætning omfattende en p2y12 receptorantagonist

Also Published As

Publication number Publication date
US20210009614A1 (en) 2021-01-14
LT3515924T (lt) 2022-03-10
JP7097369B2 (ja) 2022-07-07
US20250163086A1 (en) 2025-05-22
UA124073C2 (uk) 2021-07-14
IL265445B2 (en) 2024-05-01
JP2019529553A (ja) 2019-10-17
PH12019500567A1 (en) 2019-11-18
IL265445B1 (en) 2024-01-01
TWI752086B (zh) 2022-01-11
US20220275011A1 (en) 2022-09-01
DK3515924T3 (da) 2022-03-21
MA46266A (fr) 2019-07-31
US10730896B2 (en) 2020-08-04
RS62946B1 (sr) 2022-03-31
CN109715639A (zh) 2019-05-03
KR102552795B1 (ko) 2023-07-06
CA3037794A1 (fr) 2018-03-29
SI3515924T1 (sl) 2022-04-29
PH12019500567B1 (en) 2024-01-31
US20200017534A1 (en) 2020-01-16
EP3981774A1 (fr) 2022-04-13
US11365209B2 (en) 2022-06-21
MX2019003093A (es) 2019-07-18
WO2018055016A1 (fr) 2018-03-29
US12227532B2 (en) 2025-02-18
MX381590B (es) 2025-03-12
AU2017331930B2 (en) 2021-07-15
EA201990723A1 (ru) 2019-10-31
TW201813965A (zh) 2018-04-16
HUE057772T2 (hu) 2022-06-28
EP3515924A1 (fr) 2019-07-31
MY193080A (en) 2022-09-26
BR112019004845A2 (pt) 2019-06-04
HRP20220234T1 (hr) 2022-05-13
EP3515924B1 (fr) 2021-12-15
IL265445A (en) 2019-05-30
CN109715639B (zh) 2022-04-19
PL3515924T3 (pl) 2022-04-11
NZ750772A (en) 2023-10-27
PT3515924T (pt) 2022-03-11
ES2908572T3 (es) 2022-05-03
KR20190052704A (ko) 2019-05-16
CL2019000728A1 (es) 2019-07-05
AU2017331930A1 (en) 2019-03-07
CY1125052T1 (el) 2024-02-16

Similar Documents

Publication Publication Date Title
MA54091A (fr) Composés, compositions pharmaceutiques, procédés de préparation de composés et leur utilisation en tant qu'inhibiteurs de kinase atr
MX2021004000A (es) Derivados de piperidina.
EA201691242A1 (ru) Фармацевтические композиции, содержащие azd9291
EP4616908A3 (fr) Oxystérols et leurs procédés d'utilisation
EP3693369A3 (fr) Inhibiteurs de bromodomaine
EP2076244A4 (fr) Systèmes aqueux pour la préparation de composés pharmaceutiques à base lipidique et leurs compositions, procédés et utilisations
MX382649B (es) Análogos de pridopidina, su preparación y uso.
MD20160012A2 (ro) Formulare de inhibitori SYK
MX394588B (es) Composición farmacéutica.
MA41633B1 (fr) Composés amide en tant qu'agonistes du récepteur 5-ht4
MA37742A1 (fr) Dérivés d'oestra-1,3,5 (10), 16-tétraène substitués en position 3, leurs procédés de préparation, préparations pharmaceutiques les contenant, et leur utilisation pour la fabrication de médicaments
MA39163B1 (fr) Forme cristalline de (s)-(2-(6-chloro-7-methyl-1h-benzo[d]imidazol-2-yl)-2-methylpyrrolidin-1 -yl)(5-methoxy-2-(2h-1,2,3-triazol-2-yl)phenyl)methanone et utilisation de celle-ci en tant qu'antagonistes des recepteurs de l'orexine
EP3526203A4 (fr) Dérivés de n-aryle et de n-hétéroaryle pipéridine en tant qu'agonistes des récepteurs bêta x du foie, compositions et utilisation associées
JOP20170197B1 (ar) الصيغة الجديدة التي تشتمل على مشتق بنزيميدازول
EP3248603A4 (fr) Composition pharmaceutique destinée à la prévention, au traitement ou au ralentissement de la maladie d'alzheimer ou de la démence contenant un agent de type récepteur couplé à une protéine g 19 comme principe actif
WO2018193090A3 (fr) Procédé de préparation d'hémitartrate d'eliglustat et d'intermédiaires de celui-ci
CY1125052T1 (el) Κρυσταλλικες μορφες
MX2017015961A (es) Moduladores alostericos positivos del receptor m1 muscarinico.
NZ740587A (en) Fluoroindole derivatives as muscarinic m1 receptor positive allosteric modulators
EP3612167A4 (fr) Procédé de préparation d'une forme posologique à désintégration orale
EP4342542A3 (fr) Combinaison d'inhibiteurs de régorafénib et de pd-1/pd-l1(2) pour le traitement du cancer
MA39229A1 (fr) Pyrrolidines, térahydrofuranes et cyclopentanes substitués utiles en tant qu'antagonistes des récepteurs des orexines
BR112018073410A2 (pt) combinação de antagonistas, uso da combinação, método para o tratamento, composto, método para o tratamento de doença de alzheimer e composição farmacêutica
BR112018073419A2 (pt) combinação, uso da combinação, método para o tratamento, composto, método para o tratamento de doença de alzheimer e composição farmacêutica
WO2015138276A3 (fr) Modulateurs du récepteur orphelin lié au récepteur de l'acide rétinoïque et leurs utilisations