BR112019021868A2 - Sal de um composto derivado de aminopiridina, forma cristalina do mesmo, e processo para a preparação do mesmo - Google Patents

Sal de um composto derivado de aminopiridina, forma cristalina do mesmo, e processo para a preparação do mesmo Download PDF

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Publication number
BR112019021868A2
BR112019021868A2 BR112019021868-8A BR112019021868A BR112019021868A2 BR 112019021868 A2 BR112019021868 A2 BR 112019021868A2 BR 112019021868 A BR112019021868 A BR 112019021868A BR 112019021868 A2 BR112019021868 A2 BR 112019021868A2
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BR
Brazil
Prior art keywords
same
crystalline form
preparation
salt
aminopyridine
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BR112019021868-8A
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English (en)
Inventor
Ho Oh Sang
Gyun KIM Jong
Oh Se-Woong
Dong Han Tae
Yong Chung Soo
Ran Lee Seong
Bae Kim Kyeong
Sung Lee Young
Seob Shin Woo
Ju Hyun
Ki Kang Jeong
Min Park Su
Kyun Kim Dong
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Yuhan Corporation
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Application filed by Yuhan Corporation filed Critical Yuhan Corporation
Publication of BR112019021868A2 publication Critical patent/BR112019021868A2/pt

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic 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
    • 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
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C303/00Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
    • C07C303/02Preparation 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
    • C07C303/22Preparation 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C309/00Sulfonic acids; Halides, esters, or anhydrides thereof
    • C07C309/01Sulfonic acids
    • C07C309/02Sulfonic acids having sulfo groups bound to acyclic carbon atoms
    • C07C309/03Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
    • C07C309/04Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton containing only one sulfo group
    • 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

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (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)

Abstract

a presente invenção se refere a sal de mesilato inovador de n-(5-(4-(4-((dimetilamino)metil)-3-fenil-1h-pirazol-1-il)pirimidina-2-ilamino)-4-metóxi-2-morfolinofenil)acrilamida, uma forma cristalina inovadora do mesmo, e um processo para a preparação do mesmo. mais especificamente, a presente invenção se refere a um sal de mesilato de n-(5-(4-(4-((dimetilamino)metil)-3-fenil-1h-pirazol-1-il)pirimidina-2-ilamino)-4-metóxi-2-morfolinofenil)acrilamida, que é excelente em termos de estabilidade, solubilidade e biodisponibilidade, quando ele é administrado não apenas sozinho, mas também em combinação com outros fármacos e que apresenta uma alta pureza, um forma cristalina do mesmo, e um processo para a preparação do mesmo.
BR112019021868-8A 2017-04-21 2018-04-18 Sal de um composto derivado de aminopiridina, forma cristalina do mesmo, e processo para a preparação do mesmo BR112019021868A2 (pt)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
KR20170051687 2017-04-21
KR10-2017-0051687 2017-04-21
PCT/KR2018/004473 WO2018194356A1 (en) 2017-04-21 2018-04-18 Salt of an aminopyridine derivative compound, a crystalline form thereof, and a process for preparing the same

Publications (1)

Publication Number Publication Date
BR112019021868A2 true BR112019021868A2 (pt) 2020-05-26

Family

ID=63857137

Family Applications (1)

Application Number Title Priority Date Filing Date
BR112019021868-8A BR112019021868A2 (pt) 2017-04-21 2018-04-18 Sal de um composto derivado de aminopiridina, forma cristalina do mesmo, e processo para a preparação do mesmo

Country Status (23)

Country Link
US (2) US11453656B2 (pt)
EP (1) EP3612529A4 (pt)
JP (2) JP7126514B2 (pt)
KR (2) KR102629654B1 (pt)
CN (1) CN110869367B (pt)
AR (1) AR111469A1 (pt)
AU (2) AU2018256227B2 (pt)
BR (1) BR112019021868A2 (pt)
CA (1) CA3059543A1 (pt)
CO (1) CO2019011578A2 (pt)
EA (1) EA201992501A1 (pt)
IL (2) IL270018B (pt)
MA (1) MA49696A (pt)
MX (1) MX2022006357A (pt)
MY (1) MY201919A (pt)
NZ (1) NZ758443A (pt)
PH (1) PH12019502370A1 (pt)
SA (1) SA519410342B1 (pt)
SG (1) SG11201909615YA (pt)
TW (1) TWI776882B (pt)
UA (1) UA124364C2 (pt)
WO (1) WO2018194356A1 (pt)
ZA (1) ZA201907687B (pt)

Families Citing this family (9)

* 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
KR20200043618A (ko) * 2018-10-18 2020-04-28 주식회사유한양행 아미노피리미딘 유도체 또는 이의 염을 포함하는 경구투여용 약학 조성물
CN111349084B (zh) * 2018-12-21 2022-11-25 深圳市塔吉瑞生物医药有限公司 用于抑制蛋白激酶活性的氨基嘧啶类化合物
SG11202108311RA (en) 2019-02-26 2021-09-29 Janssen Biotech Inc Combination therapies and patient stratification with bispecific anti-egfr/c-met antibodies
JOP20210304A1 (ar) 2019-05-14 2023-01-30 Janssen Biotech Inc علاجات مركبة باستخدام الأجسام المضادة ثنائية النوعية المضادة لمستقبل عامل نمو البشرة (EGFR)/ مستقبل عامل نمو خلايا الكبد (c-Met) ومثبطات كيناز التيروسين الخاصة بمستقبل عامل نمو البشرة (EGFR) من الجيل الثالث
US11850248B2 (en) * 2019-05-14 2023-12-26 Yuhan Corporation Therapies with 3rd generation EGFR tyrosine kinase inhibitors
CN113840601A (zh) * 2019-05-14 2021-12-24 詹森生物科技公司 使用双特异性抗EGFR/c-Met抗体和第三代EGFR酪氨酸激酶抑制剂的组合疗法
TW202207940A (zh) * 2020-04-14 2022-03-01 美商健生生物科技公司 包含胺基嘧啶衍生物或其醫藥上可接受之鹽、水合物、或溶劑化物之用於經口投予之醫藥組成物
EP4349835A1 (en) 2021-06-01 2024-04-10 Hangzhou Solipharma Co., Ltd. Hydrate crystal form of lazertinib methanesulfonate, preparation method therefor and use thereof

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101337933B (zh) 2003-12-25 2011-03-02 卫材R&D管理有限公司 喹啉羧酰胺的甲磺酸盐的结晶(a)及其制备方法
CA2555804C (en) 2004-02-11 2012-06-26 Natco Pharma Limited Polymorphic form of imatinib mesylate and a process for its preparation
SG10201510696RA (en) * 2008-06-27 2016-01-28 Celgene Avilomics Res Inc Heteroaryl compounds and uses thereof
CZ2009570A3 (cs) 2009-08-26 2011-03-09 Zentiva, K. S. Príprava, stabilizace a využití polymorfu imatinib mesylátu pro vývoj lékových forem
CA2780892C (en) 2009-11-13 2017-02-14 Genosco Kinase inhibitors
US9006448B2 (en) * 2010-12-06 2015-04-14 Msn Laboratories Private Limited Process for the preparation of benzimidazole derivatives and its salts
WO2013014448A1 (en) 2011-07-27 2013-01-31 Astrazeneca Ab 2 - (2, 4, 5 - substituted -anilino) pyrimidine derivatives as egfr modulators useful for treating cancer
WO2015003571A1 (zh) 2013-07-08 2015-01-15 杭州普晒医药科技有限公司 达拉菲尼甲磺酸盐的新晶型及其制备方法
JP6468611B2 (ja) 2014-05-13 2019-02-13 アリアド ファーマシューティカルズ, インコーポレイテッド キナーゼ阻害のためのヘテロアリール化合物
BR112017007769B1 (pt) * 2014-10-13 2023-10-10 Yuhan Corporation Compostos derivados de aminopirimidina, composição farmacêutica que compreende os ditos compostos e uso terapêutico dos mesmos
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
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

Also Published As

Publication number Publication date
JP2020517611A (ja) 2020-06-18
IL270018B (en) 2022-08-01
JP7390444B2 (ja) 2023-12-01
NZ758443A (en) 2023-03-31
CN110869367B (zh) 2023-09-15
KR102629654B1 (ko) 2024-01-29
KR20230175161A (ko) 2023-12-29
CO2019011578A2 (es) 2020-02-28
IL294666B2 (en) 2024-05-01
IL270018A (pt) 2019-12-31
MY201919A (en) 2024-03-23
AU2018256227A1 (en) 2019-10-31
US11453656B2 (en) 2022-09-27
AR111469A1 (es) 2019-07-17
CN110869367A (zh) 2020-03-06
US20210139461A1 (en) 2021-05-13
US20230021395A1 (en) 2023-01-26
EP3612529A1 (en) 2020-02-26
EP3612529A4 (en) 2020-11-18
US11981659B2 (en) 2024-05-14
SG11201909615YA (en) 2019-11-28
ZA201907687B (en) 2023-04-26
MX2022006357A (es) 2022-06-23
IL294666B1 (en) 2024-01-01
SA519410342B1 (ar) 2023-02-09
JP7126514B2 (ja) 2022-08-26
KR20180118535A (ko) 2018-10-31
IL294666A (en) 2022-09-01
TW201841910A (zh) 2018-12-01
PH12019502370A1 (en) 2020-07-13
AU2022203486A1 (en) 2022-06-09
UA124364C2 (uk) 2021-09-01
JP2022166179A (ja) 2022-11-01
MA49696A (fr) 2020-06-03
WO2018194356A1 (en) 2018-10-25
AU2018256227B2 (en) 2022-03-03
EA201992501A1 (ru) 2020-02-18
TWI776882B (zh) 2022-09-11
CA3059543A1 (en) 2018-10-25

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