MA49696A - Sel d'un composé dérivé d'aminopyridine, forme cristalline de celui-ci, et son procédé de préparation - Google Patents

Sel d'un composé dérivé d'aminopyridine, forme cristalline de celui-ci, et son procédé de préparation

Info

Publication number
MA49696A
MA49696A MA049696A MA49696A MA49696A MA 49696 A MA49696 A MA 49696A MA 049696 A MA049696 A MA 049696A MA 49696 A MA49696 A MA 49696A MA 49696 A MA49696 A MA 49696A
Authority
MA
Morocco
Prior art keywords
salt
preparation
same
crystalline form
derivative compound
Prior art date
Application number
MA049696A
Other languages
English (en)
Inventor
Soo Yong Chung
Tae Dong Han
Hyun Ju
Jeong Ki Kang
Dong Kyun Kim
Jong Gyun Kim
Kyeong Bae Kim
Seong Ran Lee
Young Sung Lee
Sang Ho Oh
Se-Woong Oh
Su Min Park
Woo Seob Shin
Original Assignee
Yuhan Corp
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=63857137&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MA49696(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Yuhan Corp filed Critical Yuhan Corp
Publication of MA49696A publication Critical patent/MA49696A/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • 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
    • A61K31/535—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 oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/5375—1,4-Oxazines, e.g. morpholine
    • A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
    • C07C303/02—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of sulfonic acids or halides thereof
    • C07C303/22—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of sulfonic acids or halides thereof from sulfonic acids, by reactions not involving the formation of sulfo or halosulfonyl groups; from sulfonic halides by reactions not involving the formation of halosulfonyl groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
    • C07C309/01—Sulfonic acids
    • C07C309/02—Sulfonic acids having sulfo groups bound to acyclic carbon atoms
    • C07C309/03—Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
    • C07C309/04—Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton containing only one sulfo group
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic 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
    • C07D403/04—Heterocyclic 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
    • 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

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
MA049696A 2017-04-21 2018-04-18 Sel d'un composé dérivé d'aminopyridine, forme cristalline de celui-ci, et son procédé de préparation MA49696A (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
KR20170051687 2017-04-21

Publications (1)

Publication Number Publication Date
MA49696A true MA49696A (fr) 2020-06-03

Family

ID=63857137

Family Applications (1)

Application Number Title Priority Date Filing Date
MA049696A MA49696A (fr) 2017-04-21 2018-04-18 Sel d'un composé dérivé d'aminopyridine, forme cristalline de celui-ci, et son procédé de préparation

Country Status (22)

Country Link
US (3) US11453656B2 (fr)
EP (1) EP3612529A4 (fr)
JP (2) JP7126514B2 (fr)
KR (3) KR102629654B1 (fr)
CN (1) CN110869367B (fr)
AR (1) AR111469A1 (fr)
AU (2) AU2018256227B2 (fr)
CA (1) CA3059543A1 (fr)
CO (1) CO2019011578A2 (fr)
EA (1) EA201992501A1 (fr)
IL (2) IL270018B (fr)
MA (1) MA49696A (fr)
MX (2) MX392634B (fr)
MY (1) MY201919A (fr)
NZ (1) NZ758443A (fr)
PH (1) PH12019502370A1 (fr)
SA (1) SA519410342B1 (fr)
SG (1) SG11201909615YA (fr)
TW (1) TWI776882B (fr)
UA (1) UA124364C2 (fr)
WO (1) WO2018194356A1 (fr)
ZA (1) ZA201907687B (fr)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AR111469A1 (es) 2017-04-21 2019-07-17 Yuhan Corp Sal de un compuesto del derivado de aminopiridina, una forma cristalina de la misma, y un proceso para preparar la misma
FI3658552T3 (fi) 2017-07-28 2023-11-16 Yuhan Corp Menetelmä n-(5-((4-(4-((dimetyyliamino)metyyli)-3-fenyyli-1h-pyratsol-1-yyli)pyrimidin-2-yyli)amino)-4-metoksi-2-morfolinofenyyli)akryyliamidin valmistamiseksi saattamalla vastaava amiini reagoimaan 3-halopropionyylikloridin kanssa
KR20200043618A (ko) * 2018-10-18 2020-04-28 주식회사유한양행 아미노피리미딘 유도체 또는 이의 염을 포함하는 경구투여용 약학 조성물
KR101973074B1 (ko) * 2018-11-30 2019-04-26 주식회사 티움바이오 퓨로피리미딘 화합물의 염 및 결정형, 및 이를 포함하는 약학적 조성물
WO2020125391A1 (fr) * 2018-12-21 2020-06-25 深圳市塔吉瑞生物医药有限公司 Composé aminopyrimidine utilisés pour inhiber l'activité de la protéine kinase
SG11202108311RA (en) 2019-02-26 2021-09-29 Janssen Biotech Inc Combination therapies and patient stratification with bispecific anti-egfr/c-met antibodies
US11850248B2 (en) 2019-05-14 2023-12-26 Yuhan Corporation Therapies with 3rd generation EGFR tyrosine kinase inhibitors
WO2020230091A1 (fr) * 2019-05-14 2020-11-19 Janssen Biotech, Inc. Polythérapies avec des anticorps anti-egfr/c-met bispécifiques et des inhibiteurs de tyrosine kinase egfr de troisième génération
AU2020275272A1 (en) * 2019-05-14 2021-12-02 Janssen Biotech, Inc. Combination therapies with bispecific anti-EGFR/c-Met antibodies and third generation EGFR tyrosine kinase inhibitors
PH12022552076A1 (en) 2020-02-12 2023-11-29 Janssen Biotech Inc TREATMENT OF PATIENTS HAVING c-MET EXON 14 SKIPPING MUTATIONS
PH12022552454A1 (en) * 2020-04-14 2024-02-05 Janssen Biotech Inc Pharmaceutical composition for oral administration comprising aminopyrimidine derivative or pharmaceutically acceptable salt, hydrate, or solvate thereof
WO2022253261A1 (fr) 2021-06-01 2022-12-08 杭州领业医药科技有限公司 Forme cristalline d'hydrate de méthanesulfonate de lazertinib, son procédé de préparation et son utilisation
CA3228195A1 (en) 2023-05-23 2025-06-30 Janssen Biotech, Inc. Methods for treatment of non-small cell lung cancer (nsclc)
WO2025052273A1 (fr) 2023-09-05 2025-03-13 Janssen Biotech, Inc. Méthodes pour traiter le cancer du poumon non à petites cellules
WO2026042017A1 (fr) 2024-08-19 2026-02-26 Janssen Biotech, Inc. Amivantamab en association avec le lazertinib pour le traitement du cancer du poumon non à petites cellules (cpnpc)

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PL1698623T3 (pl) 2003-12-25 2015-08-31 Eisai R&D Man Co Ltd Postać krystaliczna soli 4-(3-chloro-4-(cyklopropyloaminokarbonylo)aminofenoksy)-7-metoksy-6-chinolinokarboksamidu lub jej solwatu i sposoby ich wytwarzania
US8048883B2 (en) 2004-02-11 2011-11-01 Natco Pharma Limited Polymorphic form of imatinib mesylate and a process for its preparation
TWI546290B (zh) * 2008-06-27 2016-08-21 賽基艾維洛米斯研究股份有限公司 雜芳基化合物及其用途
CZ2009570A3 (cs) 2009-08-26 2011-03-09 Zentiva, K. S. Príprava, stabilizace a využití polymorfu imatinib mesylátu pro vývoj lékových forem
MX2012005332A (es) 2009-11-13 2012-10-15 Oscotec Inc Inhibidores de cinasa.
WO2012077136A2 (fr) 2010-12-06 2012-06-14 Msn Laboratories Limited Procédé de préparation de dérivés de benzimidazole et de leurs sels
CN103702990B (zh) * 2011-07-27 2015-09-09 阿斯利康(瑞典)有限公司 2-(2,4,5-取代苯胺)嘧啶衍生物作为egfr调谐子用于治疗癌症
CN104540822B (zh) 2013-07-08 2016-08-31 杭州普晒医药科技有限公司 达拉菲尼甲磺酸盐的晶型及其制备方法
EP3143015B1 (fr) 2014-05-13 2019-02-20 ARIAD Pharmaceuticals, Inc. Composés hétéroaryl pour l'inhibition de kinase
EP3929190B1 (fr) * 2014-10-13 2024-12-25 Yuhan Corporation Composés et compositions de modulation des activités de kinase mutant egfr
CN104788427B (zh) 2015-02-05 2017-05-31 上海泓博智源医药股份有限公司 3‑(2‑嘧啶氨基)苯基丙烯酰胺类化合物及其应用
KR101794186B1 (ko) 2015-10-30 2017-11-08 한국기술교육대학교 산학협력단 전기자동차용 급전장치
AR111469A1 (es) * 2017-04-21 2019-07-17 Yuhan Corp Sal de un compuesto del derivado de aminopiridina, una forma cristalina de la misma, y un proceso para preparar la misma
KR20200043618A (ko) 2018-10-18 2020-04-28 주식회사유한양행 아미노피리미딘 유도체 또는 이의 염을 포함하는 경구투여용 약학 조성물

Also Published As

Publication number Publication date
CN110869367A (zh) 2020-03-06
JP2022166179A (ja) 2022-11-01
BR112019021868A2 (pt) 2020-05-26
JP2020517611A (ja) 2020-06-18
KR102629654B1 (ko) 2024-01-29
KR20250111074A (ko) 2025-07-22
EA201992501A1 (ru) 2020-02-18
US11981659B2 (en) 2024-05-14
IL270018B (en) 2022-08-01
AR111469A1 (es) 2019-07-17
JP7126514B2 (ja) 2022-08-26
KR20180118535A (ko) 2018-10-31
JP7390444B2 (ja) 2023-12-01
IL270018A (fr) 2019-12-31
IL294666B1 (en) 2024-01-01
MX392634B (es) 2025-03-24
US20210139461A1 (en) 2021-05-13
KR20230175161A (ko) 2023-12-29
MY201919A (en) 2024-03-23
TW201841910A (zh) 2018-12-01
US20240279203A1 (en) 2024-08-22
CO2019011578A2 (es) 2020-02-28
WO2018194356A1 (fr) 2018-10-25
CA3059543A1 (fr) 2018-10-25
IL294666B2 (en) 2024-05-01
EP3612529A4 (fr) 2020-11-18
UA124364C2 (uk) 2021-09-01
US11453656B2 (en) 2022-09-27
MX2022006357A (es) 2022-06-23
PH12019502370A1 (en) 2020-07-13
AU2018256227B2 (en) 2022-03-03
IL294666A (en) 2022-09-01
AU2022203486A1 (en) 2022-06-09
TWI776882B (zh) 2022-09-11
US12428401B2 (en) 2025-09-30
US20230021395A1 (en) 2023-01-26
EP3612529A1 (fr) 2020-02-26
AU2022203486B2 (en) 2024-06-06
CN110869367B (zh) 2023-09-15
ZA201907687B (en) 2023-04-26
SG11201909615YA (en) 2019-11-28
NZ758443A (en) 2023-03-31
AU2018256227A1 (en) 2019-10-31
SA519410342B1 (ar) 2023-02-09
KR102835717B1 (ko) 2025-07-18

Similar Documents

Publication Publication Date Title
MA49696A (fr) Sel d'un composé dérivé d'aminopyridine, forme cristalline de celui-ci, et son procédé de préparation
EP3786155A4 (fr) Forme cristalline d'un inhibiteur de c-met, forme de sel de celui-ci et son procédé de préparation
EP3502103A4 (fr) Forme cristalline, type de sel d'un dérivé de 2-hydro-pyrazole substitué et son procédé de préparation
EP3470400A4 (fr) Forme cristalline de l'ozanimod, forme cristalline de son hydrochloride et son procédé de préparation
EP3372606A4 (fr) Forme cristalline, procédé de préparation et intermédiaire d'un composé à cycle dihydropyridine
EP3453703A4 (fr) Forme cristalline e d'un sel de tafamidis méthylglucamine, son procédé de préparation et son application
ZA201801724B (en) Solid forms of isoquinolinone derivatives, process of making, compositions comprising, and methods of using the same
IL271399A (en) Methods for the preparation of heterocyclic 3,1-benzodioxole compounds
EP3412672A4 (fr) Forme cristalline a d'un agoniste de tlr7, son procédé de préparation et son utilisation
EP3904323A4 (fr) Procédé de préparation de 1,4-cyclohexanediméthanol
EP3647312A4 (fr) Forme cristalline d'azd9291 deutéré, procédé de préparation associé et utilisation correspondante
EP3610875A4 (fr) Sel agoniste du récepteur opioïde (mor), forme cristalline du sel de fumarate i correspondante et procédé de préparation de celui-ci
EP3407737A4 (fr) Procédé de préparation de poudre d'arêtes de poisson
EP3865473A4 (fr) Composé de sel de triphényl-phosphonium quaternaire, son procédé de préparation et son application
EP3327025A4 (fr) Forme a cristalline de rebaudioside d, et son procédé de préparation et son application
EP3412671A4 (fr) Sel de maléate d'agoniste du tlr7, formes cristallines c, d et e de celui-ci, procédés de préparation et utilisations du sel de maléate et de ses formes cristallines
IL259617B (en) Methods for the preparation of 3,1-benzodioxole heterocyclic compounds
EP3909953A4 (fr) Composé de sel d'upadacitinib et son procédé de préparation
EP3766869A4 (fr) Procédé simple de préparation d'avibactam
EP3981771A4 (fr) Procédé de synthèse d'un composé de furoimidazopyridine, forme cristalline d'un composé de furoimidazopyridine, et forme cristalline d'un sel de celui-ci
EP3696168A4 (fr) Procédé de préparation de 2-chloro-5-trifluorométhylpyridine
EP3665204A4 (fr) Procédé de préparation d'un amidon inhibé
EP3611160A4 (fr) Composé carboxylate d'ammonium, forme cristalline et substance amorphe de celui-ci, et son procédé de préparation
EP3511333A4 (fr) Forme cristalline et forme saline du composé 7h-pyrrolo [2,3-d]pyrimidine et son procédé de préparation
EP3837239A4 (fr) Procédé de préparation de solriamfétol et sel de celui-ci