SG11202109546RA - Synthesis of 4-amino-5-methyl-1h-pyridin-2(1h)-on (intermediate compound for the synthesis of the mr antagonist finerenone) from 2-chloro-5-methyl-4-nitro-pyridine-1-oxide using the intermediate compound 2-chloro-5-methyl-4-pyridinamine - Google Patents

Synthesis of 4-amino-5-methyl-1h-pyridin-2(1h)-on (intermediate compound for the synthesis of the mr antagonist finerenone) from 2-chloro-5-methyl-4-nitro-pyridine-1-oxide using the intermediate compound 2-chloro-5-methyl-4-pyridinamine

Info

Publication number
SG11202109546RA
SG11202109546RA SG11202109546RA SG11202109546RA SG11202109546RA SG 11202109546R A SG11202109546R A SG 11202109546RA SG 11202109546R A SG11202109546R A SG 11202109546RA SG 11202109546R A SG11202109546R A SG 11202109546RA SG 11202109546R A SG11202109546R A SG 11202109546RA
Authority
SG
Singapore
Prior art keywords
methyl
chloro
synthesis
intermediate compound
pyridinamine
Prior art date
Application number
SG11202109546RA
Other languages
English (en)
Inventor
Johannes Platzek
Kai Lovis
Original Assignee
Bayer Ag
Bayer Pharma AG
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 Bayer Ag, Bayer Pharma AG filed Critical Bayer Ag
Publication of SG11202109546RA publication Critical patent/SG11202109546RA/en

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Classifications

    • 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
    • C07D213/72Nitrogen atoms
    • C07D213/73Unsubstituted amino or imino radicals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pyridine Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
SG11202109546RA 2019-03-05 2020-02-28 Synthesis of 4-amino-5-methyl-1h-pyridin-2(1h)-on (intermediate compound for the synthesis of the mr antagonist finerenone) from 2-chloro-5-methyl-4-nitro-pyridine-1-oxide using the intermediate compound 2-chloro-5-methyl-4-pyridinamine SG11202109546RA (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP19160904 2019-03-05
PCT/EP2020/055292 WO2020178175A1 (de) 2019-03-05 2020-02-28 Synthese von 4-amino-5-methyl-1h-pyridin-2(1h)-on (zwischenverbindung der synthese des mr antagonisten finerenone) aus 2-chloro-5-methyl-4-nitro-pyridine-1-oxid über die zwischenverbindung 2-chloro-5-methyl-4-pyridinamin

Publications (1)

Publication Number Publication Date
SG11202109546RA true SG11202109546RA (en) 2021-09-29

Family

ID=65991501

Family Applications (1)

Application Number Title Priority Date Filing Date
SG11202109546RA SG11202109546RA (en) 2019-03-05 2020-02-28 Synthesis of 4-amino-5-methyl-1h-pyridin-2(1h)-on (intermediate compound for the synthesis of the mr antagonist finerenone) from 2-chloro-5-methyl-4-nitro-pyridine-1-oxide using the intermediate compound 2-chloro-5-methyl-4-pyridinamine

Country Status (16)

Country Link
US (1) US20220153699A1 (es)
EP (1) EP3935045A1 (es)
JP (1) JP2022523986A (es)
KR (1) KR20210135238A (es)
CN (1) CN113474332A (es)
AU (1) AU2020230965A1 (es)
BR (1) BR112021014815A2 (es)
CA (1) CA3132399A1 (es)
CL (1) CL2021002316A1 (es)
CO (1) CO2021011553A2 (es)
IL (1) IL285937A (es)
JO (1) JOP20210242A1 (es)
MX (1) MX2021010612A (es)
PE (1) PE20212199A1 (es)
SG (1) SG11202109546RA (es)
WO (1) WO2020178175A1 (es)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20210135509A (ko) * 2019-03-05 2021-11-15 바이엘 악티엔게젤샤프트 4-아미노-5-메틸피리돈을 제조하는 방법
CN114656400A (zh) * 2022-04-26 2022-06-24 浙江科聚生物医药有限公司 一种非奈利酮关键中间体的制备方法

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1311185A (zh) * 2000-03-03 2001-09-05 山东新华制药股份有限公司 4-氨基吡啶及衍生物的制备方法
JP2007530595A (ja) 2004-03-26 2007-11-01 バーテックス ファーマシューティカルズ インコーポレイテッド Erk2のピリジンインヒビターおよびそれらの使用
DE102007009494A1 (de) 2007-02-27 2008-08-28 Bayer Healthcare Ag Substituierte 4-Aryl-1, 4-dihydro-1,6-naphthyridinamide und ihre Verwendung
CN103193704B (zh) * 2013-04-12 2016-03-09 四川铂瑞生物医药有限公司 2-羟基-4-氨基-5-甲基吡啶杂环化合物
MY198066A (en) 2014-08-01 2023-07-31 Bayer Pharma AG Method for the preparation of (4s)- 4-(4-cyano-2-methoxyphenyl)-5-ethoxy-2,8-dimethyl-1,4-dihydro-1,6-naphthyridine-3-carbox-amide and the purification thereof for use as an active pharmaceutical ingredient

Also Published As

Publication number Publication date
CL2021002316A1 (es) 2022-04-08
EP3935045A1 (de) 2022-01-12
IL285937A (en) 2021-10-31
KR20210135238A (ko) 2021-11-12
JOP20210242A1 (ar) 2023-01-30
CO2021011553A2 (es) 2021-09-20
PE20212199A1 (es) 2021-11-16
WO2020178175A1 (de) 2020-09-10
MX2021010612A (es) 2021-09-28
CN113474332A (zh) 2021-10-01
JP2022523986A (ja) 2022-04-27
BR112021014815A2 (pt) 2021-09-28
US20220153699A1 (en) 2022-05-19
CA3132399A1 (en) 2020-09-10
AU2020230965A1 (en) 2021-09-23

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