AU2006312663B2 - Organic compounds - Google Patents

Organic compounds Download PDF

Info

Publication number
AU2006312663B2
AU2006312663B2 AU2006312663A AU2006312663A AU2006312663B2 AU 2006312663 B2 AU2006312663 B2 AU 2006312663B2 AU 2006312663 A AU2006312663 A AU 2006312663A AU 2006312663 A AU2006312663 A AU 2006312663A AU 2006312663 B2 AU2006312663 B2 AU 2006312663B2
Authority
AU
Australia
Prior art keywords
alkyl
formula
compound
salt
alkoxy
Prior art date
Legal status (The legal status 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 status listed.)
Ceased
Application number
AU2006312663A
Other languages
English (en)
Other versions
AU2006312663A1 (en
Inventor
Ludovic Bonnet
Stephan Gorsuch
Osamu Ichihara
Richard Mears
John Mykytiuk
Christine Richardson
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Novartis AG
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
Application filed by Novartis AG filed Critical Novartis AG
Publication of AU2006312663A1 publication Critical patent/AU2006312663A1/en
Application granted granted Critical
Publication of AU2006312663B2 publication Critical patent/AU2006312663B2/en
Ceased legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C231/00Preparation of carboxylic acid amides
    • C07C231/12Preparation of carboxylic acid amides by reactions not involving the formation of carboxamide groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C225/00Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones
    • C07C225/02Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones having amino groups bound to acyclic carbon atoms of the carbon skeleton
    • C07C225/14Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones having amino groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being unsaturated
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C269/00Preparation of derivatives of carbamic acid, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
    • C07C269/06Preparation of derivatives of carbamic acid, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups by reactions not involving the formation of carbamate groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C271/00Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
    • C07C271/06Esters of carbamic acids
    • C07C271/08Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
    • C07C271/10Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C271/22Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by carboxyl groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D309/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
    • C07D309/34Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D309/36Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with oxygen atoms directly attached to ring carbon atoms
    • C07D309/38Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with oxygen atoms directly attached to ring carbon atoms one oxygen atom in position 2 or 4, e.g. pyrones
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/07Optical isomers

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Pyrane Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
AU2006312663A 2005-11-08 2006-11-06 Organic compounds Ceased AU2006312663B2 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB0522789.7 2005-11-08
GBGB0522789.7A GB0522789D0 (en) 2005-11-08 2005-11-08 Organic compounds
PCT/EP2006/010612 WO2007054254A1 (en) 2005-11-08 2006-11-06 Organic compounds

Publications (2)

Publication Number Publication Date
AU2006312663A1 AU2006312663A1 (en) 2007-05-18
AU2006312663B2 true AU2006312663B2 (en) 2010-06-17

Family

ID=35516565

Family Applications (1)

Application Number Title Priority Date Filing Date
AU2006312663A Ceased AU2006312663B2 (en) 2005-11-08 2006-11-06 Organic compounds

Country Status (11)

Country Link
US (1) US20090318714A1 (https=)
EP (1) EP1948592A1 (https=)
JP (1) JP2009514914A (https=)
KR (1) KR20080065287A (https=)
CN (1) CN101304966A (https=)
AU (1) AU2006312663B2 (https=)
BR (1) BRPI0618641A2 (https=)
CA (1) CA2626705A1 (https=)
GB (1) GB0522789D0 (https=)
RU (1) RU2008122708A (https=)
WO (1) WO2007054254A1 (https=)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8203005B2 (en) 2009-10-29 2012-06-19 Carbo Design Llc Manufacturing process for enantiomerically pure 8-aryloctanoic acids as Aliskiren
WO2012078147A1 (en) * 2010-12-08 2012-06-14 Watson Laboratories, Inc. A process for the preparation of intermediates useful in the production of aliskiren
US8703976B2 (en) 2011-10-02 2014-04-22 Milan Soukup Manufacturing process for 8-aryloctanoic acids such as Aliskiren

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4178449A (en) * 1978-04-17 1979-12-11 American Cyanamid Company Pyrazolo[1,5-a]pyrimidines and imidazo-[1,5-a]pyrimidines
WO1996039400A1 (en) * 1995-06-06 1996-12-12 Neurocrine Biosciences, Inc. Amino-substituted thiadiazoles, pyrimidines, triazines or triazoles useful as ctf receptor antagonists

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03148264A (ja) * 1989-11-01 1991-06-25 Sumitomo Chem Co Ltd 5―アルキル―2,4―ジフェニルピリミジン誘導体、その製造法およびそれを有効成分とする除草剤
ES2274847T3 (es) 2000-12-14 2007-06-01 Speedel Pharma Ag Proceso para preparar ariloctanoil-amidas.
GB0419361D0 (en) 2004-08-31 2004-10-06 Novartis Ag Organic compounds

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4178449A (en) * 1978-04-17 1979-12-11 American Cyanamid Company Pyrazolo[1,5-a]pyrimidines and imidazo-[1,5-a]pyrimidines
WO1996039400A1 (en) * 1995-06-06 1996-12-12 Neurocrine Biosciences, Inc. Amino-substituted thiadiazoles, pyrimidines, triazines or triazoles useful as ctf receptor antagonists

Also Published As

Publication number Publication date
RU2008122708A (ru) 2009-12-20
US20090318714A1 (en) 2009-12-24
AU2006312663A1 (en) 2007-05-18
KR20080065287A (ko) 2008-07-11
JP2009514914A (ja) 2009-04-09
BRPI0618641A2 (pt) 2011-09-06
GB0522789D0 (en) 2005-12-14
EP1948592A1 (en) 2008-07-30
CA2626705A1 (en) 2007-05-18
WO2007054254A1 (en) 2007-05-18
CN101304966A (zh) 2008-11-12

Similar Documents

Publication Publication Date Title
US8946476B2 (en) Process for the preparation of amino acid derivatives
TWI222434B (en) Process for the preparation of substituted octanoyl amides
US8338620B2 (en) Methods for the production of C-8 lactam lactone compounds
AU2010297892B2 (en) Process for manufacture of N-acylbphenyl alanine
KR101476937B1 (ko) Nep 억제제의 제조를 위한 중간체의 제조 방법
CA2625034C (en) 3-alkyl-5-(4-alkyl-5-oxo-tetrahydrofutran-2-yl)pyrrolidin-2-one derivatives as intermediates in the synthesis of renin inhibitors
US20140213788A1 (en) Process for the preparation of alpha-acyloxy beta-formamido amides
US20100184998A1 (en) Organic compounds
WO2010034236A1 (en) Process for the manufacture of n-acylbiphenyl alanine
AU2006312663B2 (en) Organic compounds
JP3163391B2 (ja) スチルベン誘導体及びそれを含有する制癌剤
RU2418785C2 (ru) Способ получения ингибиторов ренина
CN101952242B (zh) 肾素抑制剂的汇集合成和其中有用的中间产物
US8969620B2 (en) Process for the preparation of amino acid derivatives
MORISHIMA et al. Synthesis of forphenicinol and forphenicine
US7214813B2 (en) Preparation of chiral cyclic amino acids and derivatives
WO1995014655A1 (en) Diastereoselective synthesis of hydroxyethylene dipeptide isosteres
US5710322A (en) Optically active iminocarboxylic acid derivatives
WO2017051326A1 (en) New processes and intermediates useful in synthesis of nep inhibitors
KR20020087270A (ko) 방향족 케톤화합물의 비대칭 수소전이 환원방법
JP2004203766A (ja) 光学活性1,2−ジアミン誘導体および光学活性イミダゾリジノン誘導体の製造法

Legal Events

Date Code Title Description
FGA Letters patent sealed or granted (standard patent)
MK14 Patent ceased section 143(a) (annual fees not paid) or expired