MA34464B1 - Procede pour la preparation de formes enantiomeres de derives d'acide 2,3- diaminopropionique - Google Patents

Procede pour la preparation de formes enantiomeres de derives d'acide 2,3- diaminopropionique

Info

Publication number
MA34464B1
MA34464B1 MA35657A MA35657A MA34464B1 MA 34464 B1 MA34464 B1 MA 34464B1 MA 35657 A MA35657 A MA 35657A MA 35657 A MA35657 A MA 35657A MA 34464 B1 MA34464 B1 MA 34464B1
Authority
MA
Morocco
Prior art keywords
preparation
acid derivatives
diaminopropionic acid
separation
enantiomer forms
Prior art date
Application number
MA35657A
Other languages
English (en)
Inventor
Claus-Dieter Graf
Joerg Rieke-Zapp
Original Assignee
Sanofi Sa
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=43598042&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MA34464(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Sanofi Sa filed Critical Sanofi Sa
Publication of MA34464B1 publication Critical patent/MA34464B1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24—Heterocyclic 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
    • C07D239/28—Heterocyclic 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
    • C07D239/32—One oxygen, sulfur or nitrogen atom
    • C07D239/42—One nitrogen atom
    • 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
    • A61K31/495—Heterocyclic 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
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic 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
    • C07D213/02—Heterocyclic 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
    • C07D213/04—Heterocyclic 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
    • C07D213/60—Heterocyclic 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
    • C07D213/72—Nitrogen atoms
    • C07D213/73—Unsubstituted amino or imino radicals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic 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
    • C07D213/02—Heterocyclic 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
    • C07D213/04—Heterocyclic 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
    • C07D213/60—Heterocyclic 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
    • C07D213/72—Nitrogen atoms
    • C07D213/74—Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
  • Pyridine Compounds (AREA)

Abstract

L'invention concerne un procédé pour la préparation des formes énantiomères de dérivés d'acide 2,3-diaminopropionique de formule (I), où R1, R2 et R3 sont définis comme décrit dans les revendications, par séparation d'un racémique. La séparation du racémique en ses énantiomères est effectuée par formation de sels diastéréoisomères après ajout d'un adjuvant énantiomère pur, et ensuite séparation par cristallisation fractionnée.
MA35657A 2010-08-12 2011-08-05 Procede pour la preparation de formes enantiomeres de derives d'acide 2,3- diaminopropionique MA34464B1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP10305884 2010-08-12
US201061428336P 2010-12-30 2010-12-30
PCT/EP2011/063504 WO2012019967A1 (fr) 2010-08-12 2011-08-05 Procédé pour la préparation de formes énantiomères de dérivés d'acide 2,3-diaminopropionique

Publications (1)

Publication Number Publication Date
MA34464B1 true MA34464B1 (fr) 2013-08-01

Family

ID=43598042

Family Applications (1)

Application Number Title Priority Date Filing Date
MA35657A MA34464B1 (fr) 2010-08-12 2011-08-05 Procede pour la preparation de formes enantiomeres de derives d'acide 2,3- diaminopropionique

Country Status (23)

Country Link
US (2) US8877926B2 (fr)
EP (1) EP2603491B1 (fr)
JP (1) JP6000248B2 (fr)
KR (1) KR20130099044A (fr)
CN (1) CN103209961A (fr)
AR (1) AR082621A1 (fr)
AU (1) AU2011288533A1 (fr)
BR (1) BR112013002985A2 (fr)
CA (1) CA2807979A1 (fr)
CL (1) CL2013000420A1 (fr)
CO (1) CO6690757A2 (fr)
CR (1) CR20130059A (fr)
DO (1) DOP2013000035A (fr)
EC (1) ECSP13012434A (fr)
GT (1) GT201300038A (fr)
MA (1) MA34464B1 (fr)
MX (1) MX2013001647A (fr)
PE (1) PE20131326A1 (fr)
RU (1) RU2013110525A (fr)
SG (1) SG187791A1 (fr)
TW (1) TW201221504A (fr)
UY (1) UY33552A (fr)
WO (1) WO2012019967A1 (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2631320C2 (ru) 2011-12-06 2017-09-21 Санофи Кристаллические формы [(s)-1-карбамоил-2-(фенилпиримидин-2-иламино)этил]амида 2-(2-метиламинопиримидин-4-ил)-1н-индол-5-карбоновой кислоты

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19850301A1 (de) * 1998-10-30 2000-05-04 Basf Ag Verfahren zur Racematspaltung von 2-Hydroxypropionsäuren
DE19951360A1 (de) 1999-10-26 2001-05-03 Aventis Pharma Gmbh Substituierte Indole
US7462638B2 (en) 2002-08-17 2008-12-09 Sanofi-Aventis Deutschland Gmbh Use of IκB-kinase inhibitors in pain therapy
DE10237722A1 (de) 2002-08-17 2004-08-19 Aventis Pharma Deutschland Gmbh Indol- oder Benzimidazolderivate zur Modulation der IKappaB-Kinase
DE102004033406A1 (de) * 2004-07-10 2006-02-16 Sanofi-Aventis Deutschland Gmbh Verfahren zur Herstellung der enantiomeren Formen von 2,3-Diaminopropionsäurederivaten
US20070142417A1 (en) * 2005-05-11 2007-06-21 Aventis Pharmaceuticals Inc Substantially Pure 2-{[2-(2-Methylamino-Pyrimidin-4-YL)-1H-Indole-5-Carbonyl]-Amino}-3-Phenylpyridin-2-YL-Amino)-Propionic Acid as an IkB Kinase Inhibitor
DE102005025225A1 (de) 2005-06-01 2006-12-07 Sanofi-Aventis Deutschland Gmbh Verfahren zur Herstellung von 2-(2-Amino-pyrimidin-4-yl)-1H-indol-5-carbonsäure-derivaten

Also Published As

Publication number Publication date
ECSP13012434A (es) 2013-03-28
AR082621A1 (es) 2012-12-19
CN103209961A (zh) 2013-07-17
MX2013001647A (es) 2013-03-21
AU2011288533A1 (en) 2013-02-28
CR20130059A (es) 2013-03-25
CO6690757A2 (es) 2013-06-17
CA2807979A1 (fr) 2012-02-16
US8877926B2 (en) 2014-11-04
US20130211085A1 (en) 2013-08-15
GT201300038A (es) 2015-06-24
DOP2013000035A (es) 2013-03-15
SG187791A1 (en) 2013-03-28
RU2013110525A (ru) 2014-09-20
BR112013002985A2 (pt) 2017-11-07
KR20130099044A (ko) 2013-09-05
UY33552A (es) 2012-03-30
CL2013000420A1 (es) 2013-04-05
WO2012019967A1 (fr) 2012-02-16
US9434696B2 (en) 2016-09-06
PE20131326A1 (es) 2013-11-12
TW201221504A (en) 2012-06-01
EP2603491B1 (fr) 2014-09-24
EP2603491A1 (fr) 2013-06-19
JP6000248B2 (ja) 2016-09-28
US20150018554A1 (en) 2015-01-15
JP2013533296A (ja) 2013-08-22

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