MA49700B1 - Procédé pour la préparation de n-(5-((4-(4-((diméthylamino)méthyl)-3-phényl-1h-pyrazol-1-yl)pyrimidin-2-yl)amino)-4-méthoxy-2-morpholinophényl)acrylamide par réaction de l'amine correspondante avec un 3-halo-propionyl chloride - Google Patents
Procédé pour la préparation de n-(5-((4-(4-((diméthylamino)méthyl)-3-phényl-1h-pyrazol-1-yl)pyrimidin-2-yl)amino)-4-méthoxy-2-morpholinophényl)acrylamide par réaction de l'amine correspondante avec un 3-halo-propionyl chlorideInfo
- Publication number
- MA49700B1 MA49700B1 MA49700A MA49700A MA49700B1 MA 49700 B1 MA49700 B1 MA 49700B1 MA 49700 A MA49700 A MA 49700A MA 49700 A MA49700 A MA 49700A MA 49700 B1 MA49700 B1 MA 49700B1
- Authority
- MA
- Morocco
- Prior art keywords
- preparation
- morpholinophenyl
- pyrazol
- pyrimidin
- acrylamide
- Prior art date
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
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/22—Tin compounds
- C07F7/2284—Compounds with one or more Sn-N linkages
-
- 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
- A61K31/495—Heterocyclic 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic 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
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
Abstract
La présente invention concerne un procédé amélioré pour la préparation d'un dérivé d'aminopyrimidine ou d'un sel pharmaceutiquement acceptable de celui-ci ayant une activité inhibitrice sélective vis-à-vis des protéines kinases, en particulier contre les protéines kinases pour des récepteurs du facteur de croissance épidermique mutant. La présente invention concerne également de nouveaux intermédiaires utiles pour ledit procédé et des procédés de préparation de ceux-ci.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR20170096212 | 2017-07-28 | ||
PCT/KR2018/008379 WO2019022485A1 (fr) | 2017-07-28 | 2018-07-25 | Procédé amélioré pour la préparation de dérivés d'aminopyrimidine |
Publications (2)
Publication Number | Publication Date |
---|---|
MA49700A MA49700A (fr) | 2021-03-17 |
MA49700B1 true MA49700B1 (fr) | 2023-09-27 |
Family
ID=65040211
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MA49700A MA49700B1 (fr) | 2017-07-28 | 2018-07-25 | Procédé pour la préparation de n-(5-((4-(4-((diméthylamino)méthyl)-3-phényl-1h-pyrazol-1-yl)pyrimidin-2-yl)amino)-4-méthoxy-2-morpholinophényl)acrylamide par réaction de l'amine correspondante avec un 3-halo-propionyl chloride |
Country Status (31)
Country | Link |
---|---|
US (4) | US10889578B2 (fr) |
EP (1) | EP3658552B1 (fr) |
JP (2) | JP7228562B2 (fr) |
KR (1) | KR102688084B1 (fr) |
CN (2) | CN111315742B (fr) |
AU (2) | AU2018308038B2 (fr) |
BR (1) | BR112020001278A2 (fr) |
CA (1) | CA3070069C (fr) |
CO (1) | CO2020000374A2 (fr) |
DK (1) | DK3658552T3 (fr) |
EA (1) | EA202090383A1 (fr) |
ES (1) | ES2962961T3 (fr) |
FI (1) | FI3658552T3 (fr) |
HR (1) | HRP20231191T1 (fr) |
HU (1) | HUE063533T2 (fr) |
IL (2) | IL271973B (fr) |
LT (1) | LT3658552T (fr) |
MA (1) | MA49700B1 (fr) |
MD (1) | MD3658552T2 (fr) |
MX (1) | MX2022008743A (fr) |
PH (1) | PH12020500059A1 (fr) |
PL (1) | PL3658552T3 (fr) |
PT (1) | PT3658552T (fr) |
RS (1) | RS64654B1 (fr) |
SA (2) | SA522431428B1 (fr) |
SG (1) | SG11201913517UA (fr) |
SI (1) | SI3658552T1 (fr) |
SM (1) | SMT202300339T1 (fr) |
UA (1) | UA125317C2 (fr) |
WO (1) | WO2019022485A1 (fr) |
ZA (1) | ZA202001250B (fr) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
MA49700B1 (fr) | 2017-07-28 | 2023-09-27 | Yuhan Corp | Procédé pour la préparation de n-(5-((4-(4-((diméthylamino)méthyl)-3-phényl-1h-pyrazol-1-yl)pyrimidin-2-yl)amino)-4-méthoxy-2-morpholinophényl)acrylamide par réaction de l'amine correspondante avec un 3-halo-propionyl chloride |
US11879013B2 (en) | 2019-05-14 | 2024-01-23 | Janssen Biotech, Inc. | Combination therapies with bispecific anti-EGFR/c-Met antibodies and third generation EGFR tyrosine kinase inhibitors |
US11850248B2 (en) * | 2019-05-14 | 2023-12-26 | Yuhan Corporation | Therapies with 3rd generation EGFR tyrosine kinase inhibitors |
JOP20220184A1 (ar) | 2020-02-12 | 2023-01-30 | Janssen Biotech Inc | علاج مصابي السرطان ممن لديهم طفرات تخطي c-Met إكسون14 |
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 |
US11780824B2 (en) * | 2020-12-16 | 2023-10-10 | Scinopharm Taiwan, Ltd. | Process for preparing osimertinib or a salt thereof |
CN116199701A (zh) * | 2023-02-27 | 2023-06-02 | 安徽中医药大学 | 一种基于分子内自由基环加成制备吡唑并恶嗪草酮类化合物及其制备方法 |
WO2024241273A1 (fr) | 2023-05-23 | 2024-11-28 | Janssen Biotech, Inc. | Méthodes de traitement du cancer du poumon non à petites cellules (cpnpc) |
WO2025052273A1 (fr) | 2023-09-05 | 2025-03-13 | Janssen Biotech, Inc. | Méthodes pour traiter le cancer du poumon non à petites cellules |
Family Cites Families (31)
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US5721237A (en) | 1991-05-10 | 1998-02-24 | Rhone-Poulenc Rorer Pharmaceuticals Inc. | Protein tyrosine kinase aryl and heteroaryl quinazoline compounds having selective inhibition of HER-2 autophosphorylation properties |
TW200300348A (en) | 2001-11-27 | 2003-06-01 | American Cyanamid Co | 3-cyanoquinolines as inhibitors of egf-r and her2 kinases |
GB0305929D0 (en) | 2003-03-14 | 2003-04-23 | Novartis Ag | Organic compounds |
AU2005309019A1 (en) | 2004-11-24 | 2006-06-01 | Novartis Ag | Combinations of JAK inhibitors and at least one of Bcr-Abl, Flt-3, FAK or RAF kinase inhibitors |
US20060270600A1 (en) | 2005-05-26 | 2006-11-30 | Eisuke Mekada | Anti-cancer agents |
TW200736232A (en) | 2006-01-26 | 2007-10-01 | Astrazeneca Ab | Pyrimidine derivatives |
EP2684874B1 (fr) | 2006-10-23 | 2017-05-17 | Cephalon, Inc. | Dérivés bicycliques fusionnés de 2,4-diaminopyrimidine utilisés comme inhibiteurs de alk et de c-met |
TW200840581A (en) | 2007-02-28 | 2008-10-16 | Astrazeneca Ab | Novel pyrimidine derivatives |
WO2008124085A2 (fr) | 2007-04-03 | 2008-10-16 | Exelixis, Inc. | Méthodes d'utilisation de combinaisons d'inhibiteurs de mek et de jak-2 |
KR101892989B1 (ko) * | 2008-06-27 | 2018-08-30 | 셀젠 카르 엘엘씨 | 헤테로아릴 화합물 및 이의 용도 |
JP2013507449A (ja) | 2009-10-12 | 2013-03-04 | ミレクシス, インコーポレイテッド | TBK1および/またはIKKεの阻害剤としてのアミノ−ピリミジン化合物 |
US8629132B2 (en) | 2009-11-13 | 2014-01-14 | Genosco | Kinase inhibitors |
KR101851130B1 (ko) | 2009-12-04 | 2018-04-23 | 센화 바이오사이언시즈 인코포레이티드 | Ck2 억제제로서 피라졸로피리미딘 및 관련된 헤테로사이클 |
ES2616238T3 (es) | 2010-10-06 | 2017-06-12 | Glaxosmithkline Llc, Corporation Service Company | Derivados de bencimidazol como inhibidores de PI3 quinasa |
JP5956999B2 (ja) | 2010-11-01 | 2016-07-27 | セルジーン アヴィロミクス リサーチ, インコーポレイテッド | ヘテロアリール化合物およびその使用 |
MY172110A (en) | 2010-12-13 | 2019-11-14 | Array Biopharma Inc | Substituted n-(1h-indazol-4-yl)imidazo[1,2-a]pyridine-3-carboxamide compounds as type iii receptor tyrosine kinase inhibitors |
MX2014000528A (es) | 2011-07-27 | 2014-05-01 | Astrazeneca Ab | Derivados de 2- (2, 4, 5 - anilino sustituido)pirimidina como moduladores de egfr util para el tratamiento de cancer. |
JP2015503505A (ja) | 2011-12-23 | 2015-02-02 | ミレニアム ファーマシューティカルズ, インコーポレイテッドMillennium Pharmaceuticals, Inc. | ヘテロアリールおよびその使用 |
AU2012363558C1 (en) | 2011-12-30 | 2019-08-29 | Hanmi Pharm Co., Ltd. | Thieno[3,2-d]pyrimidine derivatives having inhibitory activity for protein kinases |
CN104860891B (zh) | 2014-02-25 | 2017-06-30 | 上海海雁医药科技有限公司 | 芳氨基嘧啶类化合物及其应用以及由其制备的药物组合物和药用组合物 |
CN106687457B (zh) | 2014-05-13 | 2020-01-10 | 阿里亚德医药股份有限公司 | 用于激酶抑制的杂芳基化合物 |
CN111875585B (zh) | 2014-06-12 | 2023-06-23 | 上海艾力斯医药科技股份有限公司 | 一类激酶抑制剂 |
EP3604294B1 (fr) * | 2014-10-13 | 2021-05-05 | 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 |
AR102263A1 (es) | 2015-10-14 | 2017-02-15 | Yuhan Corp | Compuestos y composiciones para la modulación de las actividades quinasa del receptor de egf mutante |
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 |
DE102017212159A1 (de) | 2017-07-14 | 2019-01-17 | Krones Aktiengesellschaft | Verfahren und Vorrichtung zur Handhabung von Stückgütern, Artikeln und/oder Gebinden |
MA49700B1 (fr) * | 2017-07-28 | 2023-09-27 | Yuhan Corp | Procédé pour la préparation de n-(5-((4-(4-((diméthylamino)méthyl)-3-phényl-1h-pyrazol-1-yl)pyrimidin-2-yl)amino)-4-méthoxy-2-morpholinophényl)acrylamide par réaction de l'amine correspondante avec un 3-halo-propionyl chloride |
CN111032650A (zh) | 2017-07-28 | 2020-04-17 | 株式会社柳韩洋行 | 可用于合成氨基嘧啶衍生物的新型中间体、其制备方法以及使用其制备氨基嘧啶衍生物的方法 |
US11198684B2 (en) | 2017-07-28 | 2021-12-14 | Yuhan Corporation | Intermediates useful for the synthesis of a selective inhibitor against protein kinase and processes for preparing the same |
CN108826170A (zh) | 2018-06-26 | 2018-11-16 | 深圳市远润欣电子有限公司 | 局部全般照明的模式、控制方法及台灯 |
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2018
- 2018-07-25 MA MA49700A patent/MA49700B1/fr unknown
- 2018-07-25 WO PCT/KR2018/008379 patent/WO2019022485A1/fr active Application Filing
- 2018-07-25 PT PT188373609T patent/PT3658552T/pt unknown
- 2018-07-25 RS RS20230834A patent/RS64654B1/sr unknown
- 2018-07-25 SI SI201830998T patent/SI3658552T1/sl unknown
- 2018-07-25 EA EA202090383A patent/EA202090383A1/ru unknown
- 2018-07-25 MX MX2022008743A patent/MX2022008743A/es unknown
- 2018-07-25 JP JP2020504203A patent/JP7228562B2/ja active Active
- 2018-07-25 HR HRP20231191TT patent/HRP20231191T1/hr unknown
- 2018-07-25 CN CN201880048638.9A patent/CN111315742B/zh active Active
- 2018-07-25 IL IL271973A patent/IL271973B/en unknown
- 2018-07-25 LT LTEPPCT/KR2018/008379T patent/LT3658552T/lt unknown
- 2018-07-25 DK DK18837360.9T patent/DK3658552T3/da active
- 2018-07-25 HU HUE18837360A patent/HUE063533T2/hu unknown
- 2018-07-25 BR BR112020001278-5A patent/BR112020001278A2/pt unknown
- 2018-07-25 CA CA3070069A patent/CA3070069C/fr active Active
- 2018-07-25 CN CN202310702453.8A patent/CN116987112A/zh active Pending
- 2018-07-25 US US16/633,684 patent/US10889578B2/en active Active
- 2018-07-25 UA UAA202001303A patent/UA125317C2/uk unknown
- 2018-07-25 AU AU2018308038A patent/AU2018308038B2/en active Active
- 2018-07-25 EP EP18837360.9A patent/EP3658552B1/fr active Active
- 2018-07-25 KR KR1020180086376A patent/KR102688084B1/ko active Active
- 2018-07-25 PL PL18837360.9T patent/PL3658552T3/pl unknown
- 2018-07-25 ES ES18837360T patent/ES2962961T3/es active Active
- 2018-07-25 FI FIEP18837360.9T patent/FI3658552T3/fi active
- 2018-07-25 SM SM20230339T patent/SMT202300339T1/it unknown
- 2018-07-25 SG SG11201913517UA patent/SG11201913517UA/en unknown
- 2018-07-25 MD MDE20200593T patent/MD3658552T2/ro unknown
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2020
- 2020-01-07 PH PH12020500059A patent/PH12020500059A1/en unknown
- 2020-01-15 CO CONC2020/0000374A patent/CO2020000374A2/es unknown
- 2020-01-21 SA SA522431428A patent/SA522431428B1/ar unknown
- 2020-01-21 SA SA520411112A patent/SA520411112B1/ar unknown
- 2020-02-27 ZA ZA2020/01250A patent/ZA202001250B/en unknown
- 2020-12-08 US US17/115,037 patent/US11286253B2/en active Active
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2022
- 2022-03-25 US US17/704,718 patent/US11708362B2/en active Active
- 2022-04-24 IL IL292429A patent/IL292429B2/en unknown
- 2022-05-03 AU AU2022202936A patent/AU2022202936B2/en active Active
- 2022-11-18 JP JP2022184867A patent/JP7539451B2/ja active Active
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2023
- 2023-06-02 US US18/328,267 patent/US12187714B2/en active Active
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