AR086168A1 - Procesos para la elaboracion de depsipeptidos macrociclicos e intermediarios - Google Patents

Procesos para la elaboracion de depsipeptidos macrociclicos e intermediarios

Info

Publication number
AR086168A1
AR086168A1 ARP120101326A ARP120101326A AR086168A1 AR 086168 A1 AR086168 A1 AR 086168A1 AR P120101326 A ARP120101326 A AR P120101326A AR P120101326 A ARP120101326 A AR P120101326A AR 086168 A1 AR086168 A1 AR 086168A1
Authority
AR
Argentina
Prior art keywords
formula
compound
amino acid
salt
alkanoyl
Prior art date
Application number
ARP120101326A
Other languages
English (en)
Original Assignee
Novartis 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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=46317455&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AR086168(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Novartis Ag filed Critical Novartis Ag
Publication of AR086168A1 publication Critical patent/AR086168A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K1/00General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
    • C07K1/06General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length using protecting groups or activating agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K11/00Depsipeptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
    • C07K11/02Depsipeptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof cyclic, e.g. valinomycins ; Derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K11/00Depsipeptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K7/00Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
    • C07K7/04Linear peptides containing only normal peptide links
    • C07K7/06Linear peptides containing only normal peptide links having 5 to 11 amino acids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/55Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Molecular Biology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Biophysics (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Medicinal Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Peptides Or Proteins (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Cookers (AREA)
  • Cereal-Derived Products (AREA)

Abstract

Reivindicación 1: Un método o proceso para la preparación de un compuesto de depsipéptido cíclico de la fórmula (1), en donde: A1 es una fracción bivalente de un aminoácido con un grupo carboxilo o carbamoilo terminal, en especial asparagina o glutamina, y se enlaza en su lado derecho en la fórmula (1) por medio de un carbonilo con el resto de la molécula; o es alcanoílo C1-8 o hidroxi-alcanoílo C1-8 fosforilado; X se enlaza por medio de un N de A1 y es acilo, o está ausente si A1 es alcanoílo C1-8 o hidroxi-alcanoílo C1-8 fosforilado; R2 es alquilo C1-8, en especial metilo; R3 es la cadena lateral de un aminoácido, en especial de leucina, isoleucina o valina; R5 es la cadena lateral de un aminoácido, de preferencia de fenilalanina, leucina, isoleucina o valina; R6 es la cadena lateral de un hidroxi-aminoácido, en especial de tirosina; R7 es la cadena lateral de un aminoácido, de preferencia del aminoácido leucina, isoleucina o valina; e Y es hidrógeno o alquilo C1-8; o una sal del mismo, comprendiendo este método: desproteger selectivamente un compuesto de la fórmula (2) en donde Prot es un grupo protector, Y es como se define para un compuesto de la fórmula (1), y X*, A1*, R2*, R3*, R5*, R6*, y R7* corresponden a X, A1, R2, R3, R5, R6, y R7 en la fórmula (1), respectivamente, pero con la condición de que los grupos funcionales reactivos sobre estas fracciones están presentes en una forma protegida cuando menos si podrían participar en reacciones secundarias indeseadas, para dar como resultado un compuesto de la fórmula (3), en donde X*, A1*, R2*, R3*, R5*, R6*, y R7* tienen los significados definidos anteriormente, hacer reaccionar el grupo hidroxilo libre bajo condiciones de oxidación para formar un compuesto de la fórmula (4), y remover los grupos protectores restantes para proporcionar un compuesto de la fórmula (1), o una sal del mismo, y, opcionalmente, convertir un compuesto libre de la fórmula (1) en una sal, una sal de un compuesto de la fórmula (1) en una sal diferente de un compuesto de la fórmula (1) o en el compuesto libre de la fórmula (1), y/o convertir un análogo deshidratado de un compuesto de la fórmula (1) en el compuesto correspondiente de la formula (1).
ARP120101326A 2011-04-20 2012-04-18 Procesos para la elaboracion de depsipeptidos macrociclicos e intermediarios AR086168A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201161477319P 2011-04-20 2011-04-20

Publications (1)

Publication Number Publication Date
AR086168A1 true AR086168A1 (es) 2013-11-27

Family

ID=46317455

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP120101326A AR086168A1 (es) 2011-04-20 2012-04-18 Procesos para la elaboracion de depsipeptidos macrociclicos e intermediarios

Country Status (21)

Country Link
US (2) US8614289B2 (es)
EP (1) EP2699585A1 (es)
JP (2) JP5951006B2 (es)
KR (1) KR101580729B1 (es)
CN (2) CN103476789B (es)
AR (1) AR086168A1 (es)
AU (1) AU2012245980B2 (es)
BR (1) BR112013026660A2 (es)
CA (1) CA2833109A1 (es)
CL (2) CL2013003037A1 (es)
CO (1) CO6801799A2 (es)
EA (2) EA201500734A1 (es)
GT (1) GT201300256A (es)
IL (1) IL228727A0 (es)
MA (1) MA35034B1 (es)
MX (1) MX337526B (es)
PE (1) PE20141206A1 (es)
SG (1) SG193918A1 (es)
TN (1) TN2013000385A1 (es)
TW (1) TW201249863A (es)
WO (1) WO2012143888A1 (es)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MY151973A (en) 2007-08-17 2014-07-31 Novartis Ag Cyclic depsipeptides
US8614289B2 (en) 2011-04-20 2013-12-24 Novartis Ag Processes for the manufacture of macrocyclic depsipeptides and new intermediates
US8680054B2 (en) 2011-04-20 2014-03-25 Novartis Ag Suspension type topical formulations comprising cyclic depsipeptide
US9067978B2 (en) * 2012-10-09 2015-06-30 Novartis Ag Solution phase processes for the manufacture of macrocyclic depsipeptides and new intermediates
US8987413B2 (en) 2012-10-09 2015-03-24 Novartis Ag Aldehyde acetal based processes for the manufacture of macrocyclic depsipeptides and new intermediates
WO2015155676A1 (en) 2014-04-08 2015-10-15 Novartis Ag Novel aldehyde acetal based processes for the manufacture of macrocyclic depsipeptides and new intermediates
TWI749509B (zh) * 2015-05-20 2021-12-11 美商百靈佳殷格翰動物保健美國有限公司 驅蟲酯肽化合物
US10683325B2 (en) 2015-09-17 2020-06-16 Massachusetts Institute Of Technology Methods and systems for solid phase peptide synthesis
KR102031186B1 (ko) * 2017-01-11 2019-11-08 주식회사 엘지생활건강 단백질 강도 강화용 조성물
US11643438B2 (en) 2018-07-20 2023-05-09 The Board Of Regents Of The University Of Oklahoma Antimicrobial peptides and methods of use

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DE19828043A1 (de) 1998-06-24 1999-12-30 Bayer Ag Ektoparasitizide Mittel
JP2000154198A (ja) 1998-11-20 2000-06-06 Nisshin Flour Milling Co Ltd 環状デプシペプチドの固相合成方法及びその中間体
GB0108234D0 (en) * 2001-04-02 2001-05-23 Pharma Mar Sa Process for producing trunkamide A compounds
US20040110228A1 (en) 2002-04-01 2004-06-10 Mcalpine Shelli R. Combinatorial organic synthesis of unique biologically active compounds
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WO2005075667A1 (en) 2004-02-03 2005-08-18 Bayer Healthcare Ag Diagnostics and therapeutics for diseases associated with kallikrein 7 (klk7)
AU2007220042A1 (en) 2006-02-27 2007-09-07 Arizona Board Of Regents For And On Behalf Of Arizona State University Identification and use of novopeptides for the treatment of cancer
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US8614289B2 (en) 2011-04-20 2013-12-24 Novartis Ag Processes for the manufacture of macrocyclic depsipeptides and new intermediates
US8680054B2 (en) 2011-04-20 2014-03-25 Novartis Ag Suspension type topical formulations comprising cyclic depsipeptide
US8987413B2 (en) 2012-10-09 2015-03-24 Novartis Ag Aldehyde acetal based processes for the manufacture of macrocyclic depsipeptides and new intermediates
US9067978B2 (en) 2012-10-09 2015-06-30 Novartis Ag Solution phase processes for the manufacture of macrocyclic depsipeptides and new intermediates
WO2015155676A1 (en) 2014-04-08 2015-10-15 Novartis Ag Novel aldehyde acetal based processes for the manufacture of macrocyclic depsipeptides and new intermediates

Also Published As

Publication number Publication date
JP5951006B2 (ja) 2016-07-13
GT201300256A (es) 2015-02-19
PE20141206A1 (es) 2014-09-28
TW201249863A (en) 2012-12-16
CA2833109A1 (en) 2012-10-26
JP2014511899A (ja) 2014-05-19
IL228727A0 (en) 2013-12-31
EA201391554A1 (ru) 2014-11-28
EP2699585A1 (en) 2014-02-26
BR112013026660A2 (pt) 2016-09-06
CN103476789B (zh) 2016-11-09
AU2012245980B2 (en) 2015-01-29
MX2013012188A (es) 2013-11-04
US20120277406A1 (en) 2012-11-01
CL2015000688A1 (es) 2015-06-05
US9278997B2 (en) 2016-03-08
WO2012143888A1 (en) 2012-10-26
JP2016164158A (ja) 2016-09-08
KR101580729B1 (ko) 2015-12-28
CN104804072A (zh) 2015-07-29
US20140080995A1 (en) 2014-03-20
EA025546B1 (ru) 2017-01-30
CN103476789A (zh) 2013-12-25
CL2013003037A1 (es) 2014-10-03
US8614289B2 (en) 2013-12-24
EA201500734A1 (ru) 2015-11-30
AU2012245980A1 (en) 2013-10-03
CO6801799A2 (es) 2013-11-29
MX337526B (es) 2016-03-09
KR20130140204A (ko) 2013-12-23
MA35034B1 (fr) 2014-04-03
SG193918A1 (en) 2013-11-29
TN2013000385A1 (en) 2015-01-20

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