AR117573A1 - Formas cristalinas de un inhibidor tlr7 / tlr8 - Google Patents

Formas cristalinas de un inhibidor tlr7 / tlr8

Info

Publication number
AR117573A1
AR117573A1 ARP190101308A ARP190101308A AR117573A1 AR 117573 A1 AR117573 A1 AR 117573A1 AR P190101308 A ARP190101308 A AR P190101308A AR P190101308 A ARP190101308 A AR P190101308A AR 117573 A1 AR117573 A1 AR 117573A1
Authority
AR
Argentina
Prior art keywords
tlr7
crystalline forms
tlr8 inhibitor
tlr8
inhibitor
Prior art date
Application number
ARP190101308A
Other languages
English (en)
Original Assignee
Novartis Ag
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 Novartis Ag filed Critical Novartis Ag
Publication of AR117573A1 publication Critical patent/AR117573A1/es

Links

Classifications

    • 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
    • C07D471/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
    • 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
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4151,2-Diazoles
    • A61K31/41621,2-Diazoles condensed with heterocyclic ring systems
    • 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
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • 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
    • A61K31/4353Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D265/00Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
    • C07D265/281,4-Oxazines; Hydrogenated 1,4-oxazines
    • C07D265/301,4-Oxazines; Hydrogenated 1,4-oxazines not condensed with other rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Immunology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicinal Preparation (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Steroid Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

Reivindicación 1: Una forma cristalina del compuesto (S)-N-(4-((5-(1,6-dimetil-1H-pirazolo[3,4-b]piridin-4-il)-3-metil-4,5,6,7-tetrahidro-1H-pirazolo[4,3-c]piridin-1-il)metil)biciclo[2.2.2]octan-1-il)morfolina-3-carboxamida en su forma libre. Reivindicación 2: La forma cristalina de acuerdo con la reivindicación 1, que comprende la Forma A. Reivindicación 10: La forma cristalina de acuerdo con la reivindicación 9, que comprende la Forma HA.
ARP190101308A 2018-05-18 2019-05-16 Formas cristalinas de un inhibidor tlr7 / tlr8 AR117573A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2018087448 2018-05-18

Publications (1)

Publication Number Publication Date
AR117573A1 true AR117573A1 (es) 2021-08-18

Family

ID=67145832

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP190101308A AR117573A1 (es) 2018-05-18 2019-05-16 Formas cristalinas de un inhibidor tlr7 / tlr8

Country Status (13)

Country Link
US (1) US12084460B2 (es)
EP (1) EP3793998A1 (es)
JP (2) JP7407740B2 (es)
KR (1) KR20210013554A (es)
CN (1) CN112119078A (es)
AR (1) AR117573A1 (es)
AU (1) AU2019268583B2 (es)
BR (1) BR112020022738A2 (es)
CA (1) CA3097312A1 (es)
CL (1) CL2020002967A1 (es)
MX (2) MX2020012259A (es)
TW (2) TWI826446B (es)
WO (1) WO2019220390A1 (es)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111699187A (zh) 2018-02-12 2020-09-22 豪夫迈·罗氏有限公司 用于治疗和预防病毒感染的新的砜化合物和衍生物
EP3807270B1 (en) 2018-06-12 2023-09-13 F. Hoffmann-La Roche AG Novel heteroaryl heterocyclyl compounds for the treatment of autoimmune disease
US11952363B2 (en) 2018-07-23 2024-04-09 Hoffmann-La Roche Inc. Piperazine compounds for the treatment of autoimmune disease
CN112638908A (zh) 2018-09-04 2021-04-09 豪夫迈·罗氏有限公司 用于治疗自身免疫性疾病的苯并噻唑类化合物
CN112654618A (zh) 2018-09-06 2021-04-13 豪夫迈·罗氏有限公司 用于治疗自身免疫性疾病的新型环脒化合物
EP4182032A1 (en) 2020-07-14 2023-05-24 F. Hoffmann-La Roche AG Hydroisoquinoline or hydronaphthyridine compounds for the treatment of autoimmune disease
US11661431B2 (en) 2021-04-16 2023-05-30 Gilead Sciences, Inc. Thienopyrrole compounds
EP4398989A1 (en) 2021-09-10 2024-07-17 Gilead Sciences, Inc. Thienopyrrole compounds
EP4405051A1 (en) 2021-09-24 2024-07-31 F. Hoffmann-La Roche AG Pyrazolo[3,4-b]pyridine compounds for the treatment of autoimmune disease
CA3242349A1 (en) * 2022-01-11 2023-07-20 Novartis Ag Tlr7/8-antagonist for treating sjogren's syndrome or mixed connective tissue disease

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2222545A1 (en) 1995-06-07 1996-12-19 Sugen, Inc. Quinazolines and pharmaceutical compositions
CA2619462A1 (en) 2005-08-16 2007-02-22 Amgen, Inc. Phosphodiesterase 10 inhibitors
ES2637113T3 (es) 2011-01-10 2017-10-10 Infinity Pharmaceuticals, Inc. Procedimientos para preparar isoquinolinonas y formas sólidas de isoquinolinonas
BR112014019699B1 (pt) 2012-02-08 2021-12-07 Janssen Sciences Ireland Uc Derivados de piperidino-pirimidina, seu uso no tratamento de infecções virais e composição farmacêutica que os compreende
MD4659B1 (ro) 2013-07-30 2019-11-30 Gilead Connecticut Inc Polimorf al inhibitorilor SYK
WO2017032289A1 (en) 2015-08-25 2017-03-02 Beigene, Ltd. Process for preparing parp inhibitor, crystalline forms, and uses thereof
US10954233B2 (en) 2016-09-09 2021-03-23 Novartis Ag Compounds and compositions as inhibitors of endosomal toll-like receptors

Also Published As

Publication number Publication date
JP2024037930A (ja) 2024-03-19
BR112020022738A2 (pt) 2021-02-02
US20210206783A1 (en) 2021-07-08
AU2019268583A1 (en) 2020-10-29
EP3793998A1 (en) 2021-03-24
MX2023013584A (es) 2023-11-30
JP7407740B2 (ja) 2024-01-04
AU2019268583B2 (en) 2022-01-27
CA3097312A1 (en) 2019-11-21
TWI826446B (zh) 2023-12-21
JP2021523918A (ja) 2021-09-09
KR20210013554A (ko) 2021-02-04
MX2020012259A (es) 2021-01-29
TW202417000A (zh) 2024-05-01
TW202015698A (zh) 2020-05-01
WO2019220390A1 (en) 2019-11-21
US12084460B2 (en) 2024-09-10
CL2020002967A1 (es) 2021-04-30
CN112119078A (zh) 2020-12-22

Similar Documents

Publication Publication Date Title
AR117573A1 (es) Formas cristalinas de un inhibidor tlr7 / tlr8
CO2017005790A2 (es) Derivados heterocíclicos con sustituyentes que contienen azufre activos como plaguicidas
CL2017001617A1 (es) Formas sólidas de un inhibidor ask1 referencia cruzada a aplicaciones relacionadas
UY38448A (es) Compuestos de azol-amida pesticidamente activos
CL2015002304A1 (es) Formas del metil {4,6-diamino-2- [1- (2-fluorobencil)-1h-pirazolo [3,4-b] piridino-3-il] pirimidino-5-il} metil carbamato
DOP2021000038A (es) COMPUESTOS DE PIRAZOLO[3,4-b]PIRIDINA COMO INHIBIDORES DE CINASAS TAM Y MET
AR106192A1 (es) Formas cristalinas de un agente antiviral contra la hepatitis b
AR105238A1 (es) Compuestos de benzoxacepina oxazolidinona y métodos de uso
AR102977A1 (es) Inhibidores de erk
CR20120277A (es) Una forma cristalina y amorfa de genz 112638 hemitartrato como inhibidores de glucosilceramida sintasa
NI201200146A (es) Inhibidores no nucleosídicos de la transcriptasa inversa
CL2009000275A1 (es) Compuestos derivados de furo [3,2-c]piridina y tieno [3,2-c] piridina; composicion farmaceutica que los comprende; y su uso en el tratamiento del cancer.
MX2018010025A (es) Derivados de quinazolindion-6-carbonilo y su utilizacion como herbicidas.
CL2019001694A1 (es) Compuestos de pirazolopirimidina y métodos de uso de los mismos.
PE20180035A1 (es) Tableta de ribociclib
NI201100069A (es) Inhibidores de la integrasa del vih.
CL2016000695A1 (es) Un inhibidor selectivo de la fosfatidilinositol 3-quinasa-gamma
AR103350A1 (es) Composiciones del inhibidor de la nitrificación y métodos de preparación de las mismas
CR20150555A (es) Nuevos derivados de pirrolo[2,3-d]pirimidina
GB2542515A (en) Systems, methods, and kits for cleansing an ocular region
CL2016000496A1 (es) Compuestos derivados de 1,2,4-triazolo[1,5-a]-piridina, inhibidores de una janus cinasa, tal como jak1; composiciones farmacológicas; útiles para el tratamiento de enfermedades inflamatorias.
CL2021000904A1 (es) Método para convertir las formas e, f y g cristalinas de la sal de bis-bromuro de hidrógeno de (s)-n-((5-(etilsulfonil)piridin-2-il)metil)-7-isopropil-6-((trans-4-(trifluorometil) ciclohexil) metil)-6,7-dihidro-5h-pirrolo[3,4-b]piridin-3-carboxamida en la forma d cristalina de la sal de bis-bromuro de hidrógeno. solicitud divisional de la solicitud 190-2020
MX2016013265A (es) Análogos de compuestos de 4h-pirazolo[1,5-a]bencimidazol como inhibidores parp.
UY35036A (es) Nuevos compuestos inhibidores de la fosfodiesterasa del tipo 10a
AR104241A1 (es) Derivados de tetrahidrofuro tiazina como inhibidores de bace1 selectivos