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SG11201913517UA - Improved process for preparing aminopyrimidine derivatives - Google Patents

Improved process for preparing aminopyrimidine derivatives

Info

Publication number
SG11201913517UA
SG11201913517UA SG11201913517UA SG11201913517UA SG11201913517UA SG 11201913517U A SG11201913517U A SG 11201913517UA SG 11201913517U A SG11201913517U A SG 11201913517UA SG 11201913517U A SG11201913517U A SG 11201913517UA SG 11201913517U A SG11201913517U A SG 11201913517UA
Authority
SG
Singapore
Prior art keywords
improved process
aminopyrimidine derivatives
preparing
preparing aminopyrimidine
derivatives
Prior art date
Application number
SG11201913517UA
Inventor
Sang-Ho Oh
Ja-Heouk Khoo
Jong-Chul Lim
Seong-Ran Lee
Hyun Ju
Woo-Seob Shin
Dae-Gyu Park
su-min Park
Yoon-Ah Hwang
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=65040211&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=SG11201913517U(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 SG11201913517UA publication Critical patent/SG11201913517UA/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/22Tin compounds
    • C07F7/2284Compounds with one or more Sn-N linkages
    • 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
    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic 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
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Catalysts (AREA)
SG11201913517UA 2017-07-28 2018-07-25 Improved process for preparing aminopyrimidine derivatives SG11201913517UA (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
KR20170096212 2017-07-28
PCT/KR2018/008379 WO2019022485A1 (en) 2017-07-28 2018-07-25 Improved process for preparing aminopyrimidine derivatives

Publications (1)

Publication Number Publication Date
SG11201913517UA true SG11201913517UA (en) 2020-02-27

Family

ID=65040211

Family Applications (1)

Application Number Title Priority Date Filing Date
SG11201913517UA SG11201913517UA (en) 2017-07-28 2018-07-25 Improved process for preparing aminopyrimidine derivatives

Country Status (30)

Country Link
US (4) US10889578B2 (en)
EP (1) EP3658552B1 (en)
JP (2) JP7228562B2 (en)
KR (1) KR102688084B1 (en)
CN (2) CN116987112A (en)
AU (2) AU2018308038B2 (en)
BR (1) BR112020001278A2 (en)
CA (1) CA3070069C (en)
CO (1) CO2020000374A2 (en)
DK (1) DK3658552T3 (en)
EA (1) EA202090383A1 (en)
ES (1) ES2962961T3 (en)
FI (1) FI3658552T3 (en)
HR (1) HRP20231191T1 (en)
HU (1) HUE063533T2 (en)
IL (2) IL271973B (en)
LT (1) LT3658552T (en)
MA (1) MA49700B1 (en)
MD (1) MD3658552T2 (en)
MX (1) MX2022008743A (en)
PH (1) PH12020500059A1 (en)
PL (1) PL3658552T3 (en)
PT (1) PT3658552T (en)
RS (1) RS64654B1 (en)
SA (1) SA520411112B1 (en)
SG (1) SG11201913517UA (en)
SI (1) SI3658552T1 (en)
UA (1) UA125317C2 (en)
WO (1) WO2019022485A1 (en)
ZA (1) ZA202001250B (en)

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ES2962961T3 (en) * 2017-07-28 2024-03-22 Yuhan Corp Preparation procedure of n-(5-((4-(4-(dimethylamino)methyl)-3-phenyl-1h-pyrazol-1-yl)pyrimidin-2-yl)amino)-4-methoxy-2-morpholinophenyl )acrylamide by reacting the corresponding amine with a 3-halo-propionyl chloride
WO2020230091A1 (en) 2019-05-14 2020-11-19 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
US11780824B2 (en) * 2020-12-16 2023-10-10 Scinopharm Taiwan, Ltd. Process for preparing osimertinib or a salt thereof
CN116199701A (en) * 2023-02-27 2023-06-02 安徽中医药大学 Pyrazolooxazinone compound prepared based on intramolecular free radical cycloaddition and preparation method thereof

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MXPA04004969A (en) 2001-11-27 2004-08-11 Wyeth Corp 3-cyanoquinolines as inhibitors of egf-r and her2 kinases.
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JP2008520612A (en) 2004-11-24 2008-06-19 ノバルティス アクチエンゲゼルシャフト Combination of JAK inhibitor and at least one of Bcr-Abl, Flt-3, FAK or RAF kinase inhibitor
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
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JP2011526299A (en) * 2008-06-27 2011-10-06 アビラ セラピューティクス, インコーポレイテッド Heteroaryl compounds and their use
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JP5802676B2 (en) 2009-12-04 2015-10-28 センワ バイオサイエンシズ インコーポレイテッド Pyrazolopyrimidines and related heterocyclic compounds as CK2 inhibitors
PE20140192A1 (en) 2010-10-06 2014-02-24 Glaxosmithkline Llc BENZHIMIDAZOLE DERIVATIVES AS KINASE PI3 INHIBITORS
WO2012061303A1 (en) 2010-11-01 2012-05-10 Avila Therapeutics, Inc. Heteroaryl compounds and uses thereof
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
RS62542B1 (en) * 2011-07-27 2021-12-31 Astrazeneca Ab 2-(2,4,5-substituted-anilino)pyrimidine compounds
JP2015503505A (en) 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. Heteroaryl and uses thereof
WO2013100632A1 (en) 2011-12-30 2013-07-04 Hanmi Pharm Co., Ltd. THIENO[3,2-d]PYRIMIDINE DERIVATIVES HAVING INHIBITORY ACTIVITY FOR PROTEIN KINASES
CN104860891B (en) 2014-02-25 2017-06-30 上海海雁医药科技有限公司 Fragrant amino pyrimidines and its application and pharmaceutical composition prepared therefrom and Pharmaceutical composition
JP6468611B2 (en) 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 Heteroaryl compounds for kinase inhibition
WO2015188777A1 (en) 2014-06-12 2015-12-17 Shanghai Fochon Pharmaceutical Co Ltd Certain protein kinase inhibitors
KR102487451B1 (en) 2014-10-13 2023-01-11 주식회사유한양행 Compounds and compositions for modulating egfr mutant kinase activities
CN104788427B (en) 2015-02-05 2017-05-31 上海泓博智源医药股份有限公司 3 (2 pyrimdinyl-amino) phenylacryloyl amine compounds and its application
AR102263A1 (en) 2015-10-14 2017-02-15 Yuhan Corp COMPOUNDS AND COMPOSITIONS FOR THE MODULATION OF THE KINASA ACTIVITIES OF THE RECEIVER OF EGF MUTANTE
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ES2962961T3 (en) * 2017-07-28 2024-03-22 Yuhan Corp Preparation procedure of n-(5-((4-(4-(dimethylamino)methyl)-3-phenyl-1h-pyrazol-1-yl)pyrimidin-2-yl)amino)-4-methoxy-2-morpholinophenyl )acrylamide by reacting the corresponding amine with a 3-halo-propionyl chloride
CN108826170A (en) 2018-06-26 2018-11-16 深圳市远润欣电子有限公司 Mode, control method and the desk lamp of localized general lighting

Also Published As

Publication number Publication date
JP2020528440A (en) 2020-09-24
PL3658552T3 (en) 2024-02-19
ES2962961T3 (en) 2024-03-22
KR102688084B1 (en) 2024-07-24
JP2023027091A (en) 2023-03-01
MA49700A (en) 2021-03-17
US11286253B2 (en) 2022-03-29
EP3658552B1 (en) 2023-09-13
LT3658552T (en) 2023-11-27
AU2022202936A1 (en) 2022-05-26
HRP20231191T1 (en) 2024-02-02
SA520411112B1 (en) 2022-02-21
CA3070069A1 (en) 2019-01-31
UA125317C2 (en) 2022-02-16
RS64654B1 (en) 2023-10-31
SI3658552T1 (en) 2023-11-30
FI3658552T3 (en) 2023-11-16
MX2022008743A (en) 2023-02-02
PH12020500059A1 (en) 2020-09-28
JP7228562B2 (en) 2023-02-24
ZA202001250B (en) 2023-04-26
CO2020000374A2 (en) 2020-05-05
US20210269427A1 (en) 2021-09-02
AU2018308038B2 (en) 2022-02-03
US10889578B2 (en) 2021-01-12
PT3658552T (en) 2023-11-03
US20230312545A1 (en) 2023-10-05
CN111315742B (en) 2023-09-01
CA3070069C (en) 2024-02-20
NZ761156A (en) 2024-01-26
KR20190013553A (en) 2019-02-11
IL292429A (en) 2022-06-01
EP3658552A1 (en) 2020-06-03
EA202090383A1 (en) 2020-06-15
JP7539451B2 (en) 2024-08-23
IL271973B (en) 2022-08-01
AU2018308038A1 (en) 2020-01-30
IL271973A (en) 2020-02-27
EP3658552A4 (en) 2021-06-23
US20200165236A1 (en) 2020-05-28
DK3658552T3 (en) 2023-11-20
IL292429B1 (en) 2023-05-01
MA49700B1 (en) 2023-09-27
WO2019022485A1 (en) 2019-01-31
CN116987112A (en) 2023-11-03
CN111315742A (en) 2020-06-19
BR112020001278A2 (en) 2020-07-21
MD3658552T2 (en) 2024-02-29
AU2022202936B2 (en) 2023-04-27
US11708362B2 (en) 2023-07-25
IL292429B2 (en) 2023-09-01
HUE063533T2 (en) 2024-01-28
US20220281861A1 (en) 2022-09-08

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