MX2021002397A - Procesos para preparar un inhibidor de mdm2. - Google Patents

Procesos para preparar un inhibidor de mdm2.

Info

Publication number
MX2021002397A
MX2021002397A MX2021002397A MX2021002397A MX2021002397A MX 2021002397 A MX2021002397 A MX 2021002397A MX 2021002397 A MX2021002397 A MX 2021002397A MX 2021002397 A MX2021002397 A MX 2021002397A MX 2021002397 A MX2021002397 A MX 2021002397A
Authority
MX
Mexico
Prior art keywords
preparing
processes
mdm2 inhibitor
chlorophenyl
methylbutan
Prior art date
Application number
MX2021002397A
Other languages
English (en)
Inventor
Michael Corbett
Sebastien Caille
Austin Smith
Original Assignee
Amgen Inc
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 Amgen Inc filed Critical Amgen Inc
Publication of MX2021002397A publication Critical patent/MX2021002397A/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/08—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D263/10—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • C07D263/14—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms with radicals substituted by oxygen atoms
    • 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
    • A61K31/435—Heterocyclic 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
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A61K31/451—Non condensed piperidines, e.g. piperocaine having a carbocyclic group directly attached to the heterocyclic ring, e.g. glutethimide, meperidine, loperamide, phencyclidine, piminodine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/68—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
    • C07D211/72—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member 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
    • C07D211/74—Oxygen atoms
    • C07D211/76—Oxygen atoms attached in position 2 or 6
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/08—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D263/10—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • C07D263/12—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms with radicals containing only hydrogen and carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00—Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13—Crystalline forms, e.g. polymorphs

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (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)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Medicinal Preparation (AREA)

Abstract

La presente invención proporciona procesos comerciales para preparar ácido 2-((3R,5R,6S)-5-(3-clorofenil)-6-(4-clorofenil)-1-( (S)-1-(isopropilsulfonil)-3-metilbutan-2-il)-3 -metil-2- oxopiperidin-3-il)acético así como compuestos intermedios del mismo.
MX2021002397A 2018-08-31 2019-08-30 Procesos para preparar un inhibidor de mdm2. MX2021002397A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201862725574P 2018-08-31 2018-08-31
PCT/US2019/049087 WO2020047424A1 (en) 2018-08-31 2019-08-30 Processes for preparing a mdm2 inhibitor

Publications (1)

Publication Number Publication Date
MX2021002397A true MX2021002397A (es) 2021-04-29

Family

ID=69643829

Family Applications (2)

Application Number Title Priority Date Filing Date
MX2021002397A MX2021002397A (es) 2018-08-31 2019-08-30 Procesos para preparar un inhibidor de mdm2.
MX2023015251A MX2023015251A (es) 2018-08-31 2021-02-26 Procesos para preparar un inhibidor de mdm2.

Family Applications After (1)

Application Number Title Priority Date Filing Date
MX2023015251A MX2023015251A (es) 2018-08-31 2021-02-26 Procesos para preparar un inhibidor de mdm2.

Country Status (13)

Country Link
US (1) US11753386B2 (es)
EP (1) EP3843733A4 (es)
JP (2) JP7408635B2 (es)
KR (1) KR20210052497A (es)
CN (2) CN118388395A (es)
AU (1) AU2019327555A1 (es)
BR (1) BR112021003839A2 (es)
CA (1) CA3110525A1 (es)
EA (1) EA202190632A1 (es)
IL (1) IL281040B1 (es)
MX (2) MX2021002397A (es)
SG (1) SG11202101886VA (es)
WO (1) WO2020047424A1 (es)

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JO2998B1 (ar) 2010-06-04 2016-09-05 Amgen Inc مشتقات بيبيريدينون كمثبطات mdm2 لعلاج السرطان
JOP20200296A1 (ar) 2013-06-10 2017-06-16 Amgen Inc عمليات صنع وأشكال بلورية من mdm2 مثبط

Also Published As

Publication number Publication date
JP2021535130A (ja) 2021-12-16
IL281040A (en) 2021-04-29
US11753386B2 (en) 2023-09-12
IL281040B1 (en) 2024-10-01
US20210347743A1 (en) 2021-11-11
JP2024037957A (ja) 2024-03-19
BR112021003839A2 (pt) 2021-07-27
EA202190632A1 (ru) 2021-06-16
CN118388395A (zh) 2024-07-26
KR20210052497A (ko) 2021-05-10
WO2020047424A9 (en) 2020-04-30
JP7408635B2 (ja) 2024-01-05
AU2019327555A1 (en) 2021-03-18
CA3110525A1 (en) 2020-03-05
CN112912080A (zh) 2021-06-04
MX2023015251A (es) 2024-01-19
CN112912080B (zh) 2024-05-10
WO2020047424A1 (en) 2020-03-05
EP3843733A1 (en) 2021-07-07
SG11202101886VA (en) 2021-03-30
EP3843733A4 (en) 2022-08-24

Similar Documents

Publication Publication Date Title
AU2018260844A1 (en) Processes of making and crystalline forms of a MDM2 inhibitor
SG10201903532XA (en) 1-((3s,4r)-4-(3-fluorophenyl)-1-(2-methoxyethyl)pyrrolidin-3-yl)-3-(4-methyl-3-(2-methylpyrimidin-5-yl)-1-phenyl-1h-pyrazol-5-yl)urea as a trka kinase inhibitor
RS54030B1 (en) PIPERIDINONE DERIVATIVES AS MDM2 INHIBITORS FOR CANCER TREATMENT
PH12017501538A1 (en) Salts of p13k inhibitor and processes for their preparation
TN2017000530A1 (en) PROCESSES AND INTERMEDIATES FOR THE PREPARATION OF {1-(ETHYLSULFONYL)-3-[4-(7H-PYRROLO[2,3-d]PYRIMIDIN-4-YL)-1H-PYRAZOL-1-YL]AZETIDIN-3-YL}ACETONITRILE
EP4044964A4 (en) BIOACTIVE INTELLIGENT SCAFFOLDS FOR REGENERATIVE MEDICINE
BR112021020508A2 (pt) Inibidor de jak de 7h-pirrolo[2,3-d]pirimidina
MX2019011513A (es) Procesos para preparar compuestos de (ciclopentil[d]pirimidin-4-il )piperazina.
MX2023015251A (es) Procesos para preparar un inhibidor de mdm2.
EP3233824A4 (en) (s)-n-(3-(6-isopropoxypyridin-3-yl)-1h-indazol-5-yl)-1-(2-(4-(4-(1-methyl-1h-1,2,4-triazol-3-yl)phenyl)-3,6-dihydropyridin-1(2h)-yl)-2-oxoethyl)-3- (methylthio)pyrrolidine-3-carboxamide compositions for pharmaceutical preparations
PH12017500400A1 (en) Crystalline (2s)-3-[(3s,4s)-3-[(1r)-1-hydroxyethyl]-4-(4-methoxy-3-{[1-(5-methylpyridin-2-yl)azetidin-3-yl]oxy}phenyl) -3-methylpyrrolidin-1-yl]-3-oxopropane-1,2-diol
MX2021012421A (es) Procesos para preparar derivados de pirrolidina alfa-carboxamida.
EA202092787A1 (ru) Синтез типифарниба
MX2018015871A (es) Cenicriviroc purificado e intermedios purificados para fabricar cenicriviroc.