CL2013002436A1 - Proceso para preparar una forma cristalina anhidra de ((s)-1-hidroximetil-2,2-dimetilpropil)amida del acido ( 1as,5as)-2-(4-oxipirazin-2-il)-1a,2,5,5a-tetrahidro-1h-2,3-diazaciclopropa[a]pentaleno-4-carboxilico; forma cristalina; composicion farmaceutica; proceso para prepararla; solvato; y uso para tratar dolor y osteoporosis. - Google Patents

Proceso para preparar una forma cristalina anhidra de ((s)-1-hidroximetil-2,2-dimetilpropil)amida del acido ( 1as,5as)-2-(4-oxipirazin-2-il)-1a,2,5,5a-tetrahidro-1h-2,3-diazaciclopropa[a]pentaleno-4-carboxilico; forma cristalina; composicion farmaceutica; proceso para prepararla; solvato; y uso para tratar dolor y osteoporosis.

Info

Publication number
CL2013002436A1
CL2013002436A1 CL2013002436A CL2013002436A CL2013002436A1 CL 2013002436 A1 CL2013002436 A1 CL 2013002436A1 CL 2013002436 A CL2013002436 A CL 2013002436A CL 2013002436 A CL2013002436 A CL 2013002436A CL 2013002436 A1 CL2013002436 A1 CL 2013002436A1
Authority
CL
Chile
Prior art keywords
disease
crystalline form
oxipirazin
osteoporosis
tetrahydro
Prior art date
Application number
CL2013002436A
Other languages
English (en)
Spanish (es)
Inventor
Robert M Jones
Anthony C Blackburn
Sangdon Han
Biman B Pal
Jaimie Karyn Reuter
Antonio Garrido Montalban
Original Assignee
Arena Pharm Inc
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 Arena Pharm Inc filed Critical Arena Pharm Inc
Publication of CL2013002436A1 publication Critical patent/CL2013002436A1/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
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/4965Non-condensed pyrazines
    • A61K31/497Non-condensed pyrazines containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • 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

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
CL2013002436A 2011-02-25 2013-08-23 Proceso para preparar una forma cristalina anhidra de ((s)-1-hidroximetil-2,2-dimetilpropil)amida del acido ( 1as,5as)-2-(4-oxipirazin-2-il)-1a,2,5,5a-tetrahidro-1h-2,3-diazaciclopropa[a]pentaleno-4-carboxilico; forma cristalina; composicion farmaceutica; proceso para prepararla; solvato; y uso para tratar dolor y osteoporosis. CL2013002436A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201161446732P 2011-02-25 2011-02-25
US201161448542P 2011-03-02 2011-03-02

Publications (1)

Publication Number Publication Date
CL2013002436A1 true CL2013002436A1 (es) 2014-01-24

Family

ID=45841624

Family Applications (1)

Application Number Title Priority Date Filing Date
CL2013002436A CL2013002436A1 (es) 2011-02-25 2013-08-23 Proceso para preparar una forma cristalina anhidra de ((s)-1-hidroximetil-2,2-dimetilpropil)amida del acido ( 1as,5as)-2-(4-oxipirazin-2-il)-1a,2,5,5a-tetrahidro-1h-2,3-diazaciclopropa[a]pentaleno-4-carboxilico; forma cristalina; composicion farmaceutica; proceso para prepararla; solvato; y uso para tratar dolor y osteoporosis.

Country Status (20)

Country Link
US (4) US9458136B2 (enExample)
EP (3) EP3395812B8 (enExample)
JP (1) JP5945554B2 (enExample)
KR (1) KR102036932B1 (enExample)
CN (1) CN103608343B (enExample)
AU (1) AU2012222146B2 (enExample)
BR (1) BR112013021549B1 (enExample)
CA (1) CA2827057C (enExample)
CL (1) CL2013002436A1 (enExample)
CO (1) CO6852066A2 (enExample)
DK (1) DK3395812T3 (enExample)
EA (1) EA035989B1 (enExample)
ES (1) ES2932441T3 (enExample)
IL (1) IL227782A (enExample)
MX (1) MX346533B (enExample)
MY (1) MY165767A (enExample)
PH (1) PH12013501726A1 (enExample)
SG (1) SG192817A1 (enExample)
WO (1) WO2012116276A1 (enExample)
ZA (1) ZA201306402B (enExample)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SG10201404925TA (en) * 2009-08-28 2014-10-30 Arena Pharm Inc Cannabinoid receptor modulators
US9597340B2 (en) 2011-02-25 2017-03-21 Arena Pharmaceuticals, Inc. Cannabinoid receptor modulators
CN103492369B (zh) * 2011-02-25 2019-03-29 艾尼纳制药公司 大麻素受体调节剂
EA035989B1 (ru) * 2011-02-25 2020-09-09 Арена Фармасьютикалз, Инк. Кристаллические формы и способы получения модуляторов каннабиноидного рецептора
WO2016085941A1 (en) * 2014-11-25 2016-06-02 Arena Pharmaceuticals, Inc. Processes for the preparation of cannabinoid receptor modulators
MX2018012361A (es) * 2016-04-10 2019-05-30 Arena Pharm Inc Metodos de tratamiento con agonistas selectivos del receptor cb2.
EP3621619B1 (en) 2017-05-08 2023-06-28 Arena Pharmaceuticals, Inc. Compounds and methods for treatment of visceral pain
WO2018208847A1 (en) 2017-05-08 2018-11-15 Arena Pharmaceuticals, Inc. Compounds and methods for treatment of pain from inflammatory bowel disease
CN114391011A (zh) * 2019-09-12 2022-04-22 四川海思科制药有限公司 一种六氢化苯并吡唑衍生物及其制备
TW202330496A (zh) 2021-10-05 2023-08-01 美商艾尼納製藥公司 用於製備大麻素受體調節劑之結晶形式及方法

Family Cites Families (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3964478B2 (ja) 1995-06-30 2007-08-22 エーザイ・アール・アンド・ディー・マネジメント株式会社 ヘテロ環含有カルボン酸誘導体及びそれを含有する医薬
AU781266B2 (en) 1999-04-28 2005-05-12 Sanofi-Aventis Deutschland Gmbh Di-aryl acid derivatives as PPAR receptor ligands
WO2003049727A1 (en) 2001-12-07 2003-06-19 Virginia Commonwealth University Treatment of neoplasia
SE0300010D0 (sv) 2003-01-07 2003-01-07 Astrazeneca Ab Novel Compounds
WO2005123677A1 (en) 2004-06-16 2005-12-29 Actelion Pharmaceuticals Ltd 4-carbonyl substituted 1,1,2-trimethyl-1a,4,5,5a-tetrahydro-1h-4-aza-cyclopropa'a!pentalene derivatives as agonists for the g-protein-coupled receptor s1p1/edg1 and immunosuppressive agents
BRPI0513104A (pt) 2004-07-12 2008-04-29 Cadila Healthcare Ltd composto, composição farmacêutica, método para o tratamento de doenças associadas com os receptores de canabinóide, medicamento para o tratamento/redução de doenças associadas com os receptores de canabinóides, uso do composto, processo para a preparação do composto e intermediário
FR2875230A1 (fr) * 2004-09-13 2006-03-17 Sanofi Aventis Sa Derives de pyrazole condense, leur preparation et leur application en therapeutique
DE102004054666A1 (de) 2004-11-12 2006-05-18 Bayer Cropscience Gmbh Substituierte Pyrazol-3-carboxamide, Verfahren zur Herstellung und Verwendung als Herbizide und Pflanzenwachstumsregulatoren
PE20060949A1 (es) 2004-12-23 2006-10-11 Arena Pharm Inc Derivados fusionados de pirazol como agonistas del receptor de niacina
UA93390C2 (ru) * 2005-06-02 2011-02-10 Гленмарк Фармасьютикалс C.A. Лиганды каннабиноидных рецепторов, фармацевтическая композиция (варианты), которая их содержит, и способ их получения
CA2613678A1 (en) * 2005-06-02 2006-12-07 Glenmark Pharmaceuticals S.A. Novel cannabinoid receptor ligands, pharmaceutical compositions containing them, and process for their preparation
ATE459352T1 (de) 2006-07-04 2010-03-15 Janssen Pharmaceutica Nv Benzimidazol-cannabinoid-agonisten mit einer substituierten heterocyclischen gruppe
KR20090069318A (ko) 2006-09-25 2009-06-30 베링거 인겔하임 인터내셔날 게엠베하 Cb2 수용체를 조절하는 화합물
US8481574B2 (en) 2006-10-12 2013-07-09 Abbott Laboratories Compounds as cannabinoid receptor ligands
WO2008048914A1 (en) 2006-10-17 2008-04-24 Boehringer Ingelheim International Gmbh Polycyclic compounds which modulate the cb2 receptor
RU2009117203A (ru) 2006-11-03 2010-12-10 Гленмарк Фармасеутикалс С.А. (Ch) Новые лиганды каннабиноидных рецепторов, фармацевтические композиции, содержащие данные лиганды, и способы их получения
US8173638B2 (en) 2006-11-21 2012-05-08 Boehringer Ingelheim International Gmbh Compounds which modulate the CB2 receptor
WO2008085302A1 (en) 2006-12-20 2008-07-17 Merck & Co., Inc. Imidazopyridine analogs as cb2 receptor modulators, useful in the treatment of pain, respiratory and non-respiratory diseases
US20080161340A1 (en) 2006-12-20 2008-07-03 Cara Therapeutics, Inc. Tetrahydroquinilinones, tetrahydronaphthyridones and derivatives thereof
WO2008109007A1 (en) 2007-03-02 2008-09-12 Cara Therapeutics, Inc. Bridged phenanthridines
WO2008114619A1 (ja) 2007-03-16 2008-09-25 Kyocera Corporation 誘電体磁器およびコンデンサ
ES2548764T3 (es) 2007-03-30 2015-10-20 Janssen Pharmaceutica N.V. Agonistas de cannabinoides de bencimidazol
WO2008157500A1 (en) 2007-06-17 2008-12-24 Kalypsys, Inc. Aminoquinazoline cannabinoid receptor modulators for treatment of disease
JP5485148B2 (ja) 2007-06-21 2014-05-07 カラ セラピューティクス インコーポレイテッド 置換イミダゾ複素環
US8338623B2 (en) 2007-07-09 2012-12-25 Abbvie Inc. Compounds as cannabinoid receptor ligands
US7943658B2 (en) 2007-07-23 2011-05-17 Bristol-Myers Squibb Company Indole indane amide compounds useful as CB2 agonists and method
US20120004222A1 (en) 2007-08-21 2012-01-05 Zhicai Wu Cb2 receptor ligands for the treatment of pain
UA104010C2 (en) 2008-12-18 2013-12-25 Эли Лилли Энд Компани Purine compounds
US7741350B1 (en) * 2009-01-28 2010-06-22 Cara Therapeutics, Inc. Bicyclic pyrazolo-heterocycles
US8653127B2 (en) 2009-01-28 2014-02-18 Cara Therapeutics, Inc. Bicyclic pyrazolo-heterocycles
SG10201404925TA (en) * 2009-08-28 2014-10-30 Arena Pharm Inc Cannabinoid receptor modulators
WO2012116278A1 (en) 2011-02-25 2012-08-30 Arena Pharmaceuticals, Inc. Cannabinoid receptor modulators
CN103492369B (zh) * 2011-02-25 2019-03-29 艾尼纳制药公司 大麻素受体调节剂
US9597340B2 (en) 2011-02-25 2017-03-21 Arena Pharmaceuticals, Inc. Cannabinoid receptor modulators
EA035989B1 (ru) * 2011-02-25 2020-09-09 Арена Фармасьютикалз, Инк. Кристаллические формы и способы получения модуляторов каннабиноидного рецептора

Also Published As

Publication number Publication date
MY165767A (en) 2018-04-23
AU2012222146A1 (en) 2013-09-19
US10981895B2 (en) 2021-04-20
US20210380560A1 (en) 2021-12-09
EP4166552B1 (en) 2025-03-19
BR112013021549B1 (pt) 2022-01-11
US9458136B2 (en) 2016-10-04
US20170144993A1 (en) 2017-05-25
JP5945554B2 (ja) 2016-07-05
IL227782A0 (en) 2013-09-30
SG192817A1 (en) 2013-09-30
US11560369B2 (en) 2023-01-24
AU2012222146B2 (en) 2017-05-11
DK3395812T3 (da) 2022-11-28
EP3395812B8 (en) 2022-11-02
US20140135345A1 (en) 2014-05-15
CN103608343A (zh) 2014-02-26
NZ614787A (en) 2014-08-29
EA201391233A1 (ru) 2014-02-28
JP2014506602A (ja) 2014-03-17
US10183930B2 (en) 2019-01-22
EP3395812A1 (en) 2018-10-31
ES2932441T3 (es) 2023-01-19
CA2827057C (en) 2022-06-07
US20190308952A1 (en) 2019-10-10
BR112013021549A2 (pt) 2016-11-01
CO6852066A2 (es) 2014-01-30
IL227782A (en) 2017-02-28
PH12013501726A1 (en) 2014-01-13
WO2012116276A1 (en) 2012-08-30
ZA201306402B (en) 2022-03-30
EA035989B1 (ru) 2020-09-09
EP4166552A1 (en) 2023-04-19
KR20140025353A (ko) 2014-03-04
MX2013009760A (es) 2014-06-11
EP3395812B1 (en) 2022-09-28
MX346533B (es) 2017-03-14
KR102036932B1 (ko) 2019-10-25
CN103608343B (zh) 2019-02-01
EP2678330A1 (en) 2014-01-01
CA2827057A1 (en) 2012-08-30

Similar Documents

Publication Publication Date Title
CL2013002436A1 (es) Proceso para preparar una forma cristalina anhidra de ((s)-1-hidroximetil-2,2-dimetilpropil)amida del acido ( 1as,5as)-2-(4-oxipirazin-2-il)-1a,2,5,5a-tetrahidro-1h-2,3-diazaciclopropa[a]pentaleno-4-carboxilico; forma cristalina; composicion farmaceutica; proceso para prepararla; solvato; y uso para tratar dolor y osteoporosis.
CL2016003247A1 (es) Composiciones y métodos para la expresión de arns guía usando el promotor h1
MX395148B (es) Método para sintetizar los análogos de hormona tiroidea y leucocitos polimorfonucleares de los mismos.
MX2015014487A (es) Modificación dirigida del genoma de rata.
MY159252A (en) Process for the preparation of dopo-derived compounds and compositions thereof
MX2009010361A (es) Anticuerpos il-12 anti-humanos cristalinos.
MX2013013144A (es) Metodo para la produccion de un dimero mdi.
MX377644B (es) 6.7.beta-epóxidos esteroideos como intermedios químicos.
GB201119306D0 (en) Process for continuously producing thermoplastically processable polyurethanes
PH12013500694A1 (en) Process for manufacturing dihydropteridinones and intermediates thereof
MY169924A (en) Clear hydrophobic tpu
IN2014DN02166A (enExample)
MD20120129A2 (en) Process for the preparation of perindopril L-arginine salt
IN2014MN02314A (enExample)
MX2023009372A (es) Proceso para la preparacion de compuestos enlazantes de farmaco.
CN107001244A (zh) 异氰酸酯化合物的制造方法
BR112015010455A2 (pt) método para produção, isolamento e purificação de anti-triptase humana recombinante (osraat) a partir de sementes de arroz
MY160912A (en) Formulations
WO2016084100A3 (en) Novel and efficient method for large scale synthesis of romidepsin
CY1118348T1 (el) Μεθοδος παρασκευης μεταξαλονης
IN2014DN08226A (enExample)
PH12016500749B1 (en) A method for preparing an intermediate of iopromide
PH12021550022A1 (en) Spirobiindane derivatives and a process for preparation thereof
RU2013138900A (ru) Способ кормления гусят-бройлеров
Koval'skaya et al. (-)-Sclareol conversion in the Ritter’s reaction conditions