RS65914B1 - Fenil-2-hidroksi-acetilamino-2-metil-fenil jedinjenja - Google Patents

Fenil-2-hidroksi-acetilamino-2-metil-fenil jedinjenja

Info

Publication number
RS65914B1
RS65914B1 RS20240950A RSP20240950A RS65914B1 RS 65914 B1 RS65914 B1 RS 65914B1 RS 20240950 A RS20240950 A RS 20240950A RS P20240950 A RSP20240950 A RS P20240950A RS 65914 B1 RS65914 B1 RS 65914B1
Authority
RS
Serbia
Prior art keywords
compound
methyl
amino
formula
phenyl
Prior art date
Application number
RS20240950A
Other languages
English (en)
Serbian (sr)
Inventor
Marta Maria Cifuentes-Garcia
Maria Cristina Garcia-Paredes
Original Assignee
Lilly Co Eli
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 Lilly Co Eli filed Critical Lilly Co Eli
Publication of RS65914B1 publication Critical patent/RS65914B1/sr

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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4418Non condensed pyridines; Hydrogenated derivatives thereof having a carbocyclic group directly attached to the heterocyclic ring, e.g. cyproheptadine
    • 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
    • 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
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/78Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/81Amides; Imides
    • C07D213/82Amides; Imides in position 3
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D241/00Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
    • C07D241/02Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
    • C07D241/10Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D241/14Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D241/24Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D241/26Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with nitrogen atoms directly attached to ring carbon atoms
    • C07D241/28Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with nitrogen atoms directly attached to ring carbon atoms in which said hetero-bound carbon atoms have double bonds to oxygen, sulfur or nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pyridine Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
RS20240950A 2017-04-18 2018-04-11 Fenil-2-hidroksi-acetilamino-2-metil-fenil jedinjenja RS65914B1 (sr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP17382207 2017-04-18
EP21211015.9A EP4039675B1 (en) 2017-04-18 2018-04-11 Phenyl-2-hydroxy-acetylamino-2-methyl-phenyl compounds

Publications (1)

Publication Number Publication Date
RS65914B1 true RS65914B1 (sr) 2024-10-31

Family

ID=58606227

Family Applications (2)

Application Number Title Priority Date Filing Date
RS20240950A RS65914B1 (sr) 2017-04-18 2018-04-11 Fenil-2-hidroksi-acetilamino-2-metil-fenil jedinjenja
RS20220154A RS62933B1 (sr) 2017-04-18 2018-04-11 Fenil-2-hidroksi-acetilamino-2-metil-fenil jedinjenja

Family Applications After (1)

Application Number Title Priority Date Filing Date
RS20220154A RS62933B1 (sr) 2017-04-18 2018-04-11 Fenil-2-hidroksi-acetilamino-2-metil-fenil jedinjenja

Country Status (30)

Country Link
US (2) US11655214B2 (enExample)
EP (2) EP3612519B1 (enExample)
JP (2) JP7110232B2 (enExample)
KR (2) KR20230129627A (enExample)
CN (2) CN110831927B (enExample)
AU (2) AU2018255191B2 (enExample)
BR (1) BR112019021867A2 (enExample)
CO (1) CO2019012767A2 (enExample)
CR (1) CR20190519A (enExample)
CY (1) CY1125150T1 (enExample)
DK (2) DK3612519T3 (enExample)
ES (2) ES2906847T3 (enExample)
FI (1) FI4039675T3 (enExample)
HR (2) HRP20241188T1 (enExample)
HU (2) HUE068023T2 (enExample)
IL (2) IL270005B (enExample)
LT (2) LT3612519T (enExample)
MX (2) MX389724B (enExample)
MY (1) MY199442A (enExample)
NZ (1) NZ758291A (enExample)
PH (1) PH12019502363B1 (enExample)
PL (2) PL3612519T3 (enExample)
PT (2) PT3612519T (enExample)
RS (2) RS65914B1 (enExample)
SA (1) SA519410320B1 (enExample)
SG (1) SG11201909680UA (enExample)
SI (2) SI4039675T1 (enExample)
SM (2) SMT202400357T1 (enExample)
WO (1) WO2018194885A1 (enExample)
ZA (1) ZA201906811B (enExample)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SG11201909680UA (en) * 2017-04-18 2019-11-28 Lilly Co Eli Phenyl-2-hydroxy-acetylamino-2-methyl-phenyl compounds
CN112166187B (zh) 2018-03-26 2025-06-20 西奈山伊坎医学院 治疗微小残留癌的方法
JP2022546410A (ja) * 2019-08-29 2022-11-04 ヒベルセル, インコーポレイテッド Perk阻害化合物
US12331054B2 (en) 2019-08-29 2025-06-17 Hibercell, Inc. Perk inhibiting imidazolopyrazine compounds
KR20220066290A (ko) * 2019-08-29 2022-05-24 히버셀, 인크. Perk 억제 피롤로피리미딘 화합물
WO2021041976A1 (en) 2019-08-29 2021-03-04 Hibercell, Inc. Perk inhibiting indolinyl compounds
WO2021231782A1 (en) * 2020-05-13 2021-11-18 Hibercell, Inc. Perk inhibitors for treating viral infections
WO2021231788A1 (en) * 2020-05-13 2021-11-18 Hibercell, Inc. Perk inhibiting pyrrolopyrimidine compounds to treat viral infections
CN113234029B (zh) * 2021-05-25 2022-03-22 白银康寓信生物科技有限公司 一种2-氨基-3,5-二卤代吡嗪的合成方法
WO2024206890A1 (en) * 2023-03-30 2024-10-03 Hibercell, Inc. Crystalline forms of (r)-2-amino-5-(4-(2-(3,5-difluorophenyl)-2-hydroxyacetamido)-2-methylphenyl)-n-isopropylnicotinamide and methods for using the same
GB202407386D0 (en) 2024-05-24 2024-07-10 Apollo Ap45 Ltd 1H-pyrazolo(4,3-D)pyrimidine derivatives

Family Cites Families (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7863444B2 (en) 1997-03-19 2011-01-04 Abbott Laboratories 4-aminopyrrolopyrimidines as kinase inhibitors
EP0970084B1 (en) 1997-03-19 2003-06-04 Basf Aktiengesellschaft Pyrrolo 2,3d]pyrimidines and their use as tyrosine kinase inhibitors
TW200306819A (en) * 2002-01-25 2003-12-01 Vertex Pharma Indazole compounds useful as protein kinase inhibitors
JP4901102B2 (ja) 2002-05-03 2012-03-21 エクセリクシス, インク. プロテインキナーゼモジュレーターおよびその使用方法
NZ544920A (en) * 2003-07-23 2009-11-27 Bayer Healthcare Llc 4{4-[3-(4-chloro-3-trifluoromethylphenyl)-ureido]-3-fluorophenoxy}-pyridine-2-carboxylic acid methylamide and metabolites for the treatment and prevention of diseases and conditions
TW200804345A (en) * 2005-08-30 2008-01-16 Novartis Ag Substituted benzimidazoles and methods of preparation
WO2007026920A2 (en) * 2005-09-02 2007-03-08 Astellas Pharma Inc. Amide derivatives as rock inhibitors
CA2716826C (en) 2008-02-25 2017-05-09 Prometheus Laboratories Inc. Drug selection for breast cancer therapy using antibody-based arrays
US20120014911A1 (en) 2009-01-09 2012-01-19 Serge Fuchs Regulators of the Interferon-Alpha Receptor 1 (IFNAR1) Chain of the Interferon Receptor
US8598156B2 (en) 2010-03-25 2013-12-03 Glaxosmithkline Llc Chemical compounds
WO2014170706A1 (en) 2013-04-15 2014-10-23 Università Degli Studi Di Bari Galloyl benzamide-based compounds as jnk modulators
WO2015056180A1 (en) 2013-10-15 2015-04-23 Glaxosmithkline Intellectual Property (No.2) Limited Indoline derivatives as inhibitors of perk
JP6493218B2 (ja) 2013-11-08 2019-04-03 小野薬品工業株式会社 ピロロピリミジン誘導体
EP3116877A1 (en) 2014-03-11 2017-01-18 Glaxosmithkline Intellectual Property (No. 2) Limited Chemical compounds acting as perk inhibitors
WO2016004254A1 (en) 2014-07-01 2016-01-07 The Regents Of The University Of California Combined modulation of ire1
EA039885B1 (ru) 2014-11-14 2022-03-23 НЕРВИАНО МЕДИКАЛ САЙЕНСИЗ С.р.л. Производные 6-амино-7-бицикло-7-деазапурина в качестве ингибиторов протеинкиназы
GB201508747D0 (en) 2015-05-21 2015-07-01 Univ Edinburgh Compounds
KR20180048635A (ko) * 2015-07-24 2018-05-10 블루프린트 메디신즈 코포레이션 Kit 및 pdgfr에 관련된 장애를 치료하는데 유용한 조성물
KR102327917B1 (ko) 2016-07-07 2021-11-17 주식회사 대웅제약 신규한 4-아미노피라졸로[3,4-d]피리미디닐아자바이사이클로 유도체 및 이를 포함하는 약학 조성물
US20190241573A1 (en) 2016-07-20 2019-08-08 Glaxosmithkline Intellectual Property Development Limited Isoquinoline derivatives as perk inhibitors
CN106748989B (zh) 2016-11-14 2020-03-17 西安交通大学 一种具有抗肿瘤活性的二芳基脲类化合物及其制备方法和应用
EP3573608A1 (en) 2017-01-30 2019-12-04 Université de Liège Perk and ire-1a inhibitors against neurodevelopmental disorders
SG11201909680UA (en) 2017-04-18 2019-11-28 Lilly Co Eli Phenyl-2-hydroxy-acetylamino-2-methyl-phenyl compounds
US11673891B2 (en) 2017-11-14 2023-06-13 Dana-Farber Cancer Institute, Inc. Imidazopyrimidine compounds and uses thereof
EP3492454A1 (en) 2017-11-30 2019-06-05 Step Pharma S.A.S. Compounds
CN112166187B (zh) 2018-03-26 2025-06-20 西奈山伊坎医学院 治疗微小残留癌的方法
CA3104398A1 (en) 2018-07-06 2020-01-09 Gilead Sciences, Inc. Therapeutic heterocyclic compounds
EP3860578A1 (en) 2018-10-01 2021-08-11 Institut National de la Santé et de la Recherche Médicale (INSERM) Use of inhibitors of stress granule formation for targeting the regulation of immune responses

Also Published As

Publication number Publication date
DK4039675T3 (da) 2024-09-02
CN110831927A (zh) 2020-02-21
SI3612519T1 (sl) 2022-04-29
ZA201906811B (en) 2021-01-27
MX2019012428A (es) 2022-01-28
CN110831927B (zh) 2023-07-14
RU2019136694A (ru) 2021-05-18
SI4039675T1 (sl) 2024-10-30
MX389724B (es) 2025-03-20
JP7331212B2 (ja) 2023-08-22
JP2022141835A (ja) 2022-09-29
HUE057745T2 (hu) 2022-06-28
PL4039675T3 (pl) 2025-01-07
EP3612519A1 (en) 2020-02-26
IL288822A (en) 2022-02-01
JP2021517555A (ja) 2021-07-26
CO2019012767A2 (es) 2020-04-01
LT3612519T (lt) 2022-03-25
SMT202200100T1 (it) 2022-03-21
JP7110232B2 (ja) 2022-08-01
WO2018194885A1 (en) 2018-10-25
IL270005B (en) 2022-01-01
DK3612519T3 (da) 2022-03-07
NZ758291A (en) 2025-11-28
EP4039675B1 (en) 2024-06-12
MX2022001310A (es) 2022-03-02
CR20190519A (es) 2020-03-06
EP4039675A1 (en) 2022-08-10
HRP20241188T1 (hr) 2024-12-06
ES2988739T3 (es) 2024-11-21
LT4039675T (lt) 2024-10-10
EP3612519B1 (en) 2021-12-01
FI4039675T3 (fi) 2024-09-10
KR20230129627A (ko) 2023-09-08
AU2022206702B2 (en) 2024-04-11
CA3060564A1 (en) 2018-10-25
PT3612519T (pt) 2022-02-22
MY199442A (en) 2023-10-28
SMT202400357T1 (it) 2024-11-15
PL3612519T3 (pl) 2022-05-02
US20210114985A1 (en) 2021-04-22
CY1125150T1 (el) 2023-06-09
KR20190140966A (ko) 2019-12-20
SA519410320B1 (ar) 2022-05-08
PH12019502363A1 (en) 2020-12-07
US20230373922A1 (en) 2023-11-23
HUE068023T2 (hu) 2024-12-28
BR112019021867A2 (pt) 2020-05-26
KR102575246B1 (ko) 2023-09-06
PT4039675T (pt) 2024-09-16
CN117510405A (zh) 2024-02-06
AU2018255191A1 (en) 2019-11-07
AU2022206702A1 (en) 2022-08-11
HRP20220263T1 (hr) 2022-04-29
ES2906847T3 (es) 2022-04-20
PH12019502363B1 (en) 2023-11-15
IL288822B2 (en) 2023-06-01
RS62933B1 (sr) 2022-03-31
AU2018255191B2 (en) 2022-04-21
RU2019136694A3 (enExample) 2021-05-19
SG11201909680UA (en) 2019-11-28
US11655214B2 (en) 2023-05-23

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