MX2013002150A - Proceso para la preparacion de intermediarios para la elaboracion de inhibidores de nep. - Google Patents
Proceso para la preparacion de intermediarios para la elaboracion de inhibidores de nep.Info
- Publication number
- MX2013002150A MX2013002150A MX2013002150A MX2013002150A MX2013002150A MX 2013002150 A MX2013002150 A MX 2013002150A MX 2013002150 A MX2013002150 A MX 2013002150A MX 2013002150 A MX2013002150 A MX 2013002150A MX 2013002150 A MX2013002150 A MX 2013002150A
- Authority
- MX
- Mexico
- Prior art keywords
- nep inhibitors
- manufacture
- intermediates
- preparation
- amino
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C269/00—Preparation of derivatives of carbamic acid, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C269/06—Preparation 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/10—Antioedematous agents; Diuretics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- B01J31/12—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
- C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
- C07C271/10—Esters 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
- C07C271/22—Esters 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Hospice & Palliative Care (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Pulmonology (AREA)
- Urology & Nephrology (AREA)
- Materials Engineering (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
La invención se refiere a un nuevo proceso para producir intermediarios útiles para la elaboración de inhibidores de NEP o pro-fármacos de los mismos, en particular inhibidores de NEP que comprenden una estructura base de ácido o éster de ácido ?-amino-d-bifenil-a-metil-alcanoico, tal como el etil-éster del ácido N-(3-carboxil-1-oxo-propil)-(4S)-(p-fenil-fenil-metil)-4-ami no-(2R)-metil-butanoico o una sal del mismo.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2010076245 | 2010-08-23 | ||
PCT/EP2011/064410 WO2012025501A1 (en) | 2010-08-23 | 2011-08-22 | Process for the preparation of intermediates for the manufacture of nep inhibitors |
Publications (1)
Publication Number | Publication Date |
---|---|
MX2013002150A true MX2013002150A (es) | 2013-04-03 |
Family
ID=44658722
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2013002150A MX2013002150A (es) | 2010-08-23 | 2011-08-22 | Proceso para la preparacion de intermediarios para la elaboracion de inhibidores de nep. |
Country Status (14)
Country | Link |
---|---|
US (1) | US8835668B2 (es) |
EP (1) | EP2609075B1 (es) |
JP (1) | JP5705984B2 (es) |
KR (1) | KR101476937B1 (es) |
AU (1) | AU2011295170B2 (es) |
BR (1) | BR112013004164A2 (es) |
CA (1) | CA2806780A1 (es) |
ES (1) | ES2576179T3 (es) |
MX (1) | MX2013002150A (es) |
PL (1) | PL2609075T3 (es) |
PT (1) | PT2609075E (es) |
RU (1) | RU2588572C2 (es) |
SI (1) | SI2609075T1 (es) |
WO (1) | WO2012025501A1 (es) |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
PE20091364A1 (es) | 2008-01-17 | 2009-10-13 | Novartis Ag | Proceso para la preparacion de inhibidores de nep |
LT3218351T (lt) | 2014-11-14 | 2019-09-25 | Zentiva K.S. | Ahu-377 farmaciniu požiūriu priimtinų formų gavimo, atskyrimo ir gryninimo būdas |
TW201632493A (zh) | 2015-02-13 | 2016-09-16 | 諾華公司 | 新穎方法 |
WO2016135751A1 (en) | 2015-02-25 | 2016-09-01 | Mylan Laboratories Limited | Novel process for the preparation of sacubitril and its intermediates |
WO2017051326A1 (en) | 2015-09-23 | 2017-03-30 | Novartis Ag | New processes and intermediates useful in synthesis of nep inhibitors |
CA3006254A1 (en) | 2015-12-10 | 2017-06-15 | Novartis Ag | New process and intermediates |
MX2018007129A (es) | 2015-12-11 | 2018-11-09 | Zentiva Ks | Formas solidas de ester etilico del acido (2r,4s)-5-(bifenil-4-il) -4-[(3-carboxipropionil)amino]-2-metil-pentanoico, sus sales y un metodo de preparacion. |
CN109415308B (zh) | 2016-07-05 | 2022-09-06 | 诺华股份有限公司 | 用于早期沙卡布曲中间体的新方法 |
US10851059B2 (en) | 2016-08-17 | 2020-12-01 | Novartis Ag | Processes and intermediates for NEP inhibitor synthesis |
JP7138106B2 (ja) | 2016-12-23 | 2022-09-15 | ノバルティス アーゲー | 初期サクビトリル中間体のための新規な方法 |
CN106946742A (zh) * | 2017-03-28 | 2017-07-14 | 常州沃腾化工科技有限公司 | 一种三苯基氧磷含量低的沙库必曲中间体的制备方法 |
CN109503404A (zh) * | 2018-12-28 | 2019-03-22 | 凯瑞斯德生化(苏州)有限公司 | 一种lcz-696关键中间体的制备方法 |
Family Cites Families (32)
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JPS5015793B2 (es) | 1972-06-07 | 1975-06-07 | ||
JPS53103412A (en) * | 1977-02-18 | 1978-09-08 | Kuraray Co Ltd | Preparation of farnesyl acetic acid or its ester |
US4219683A (en) * | 1978-09-25 | 1980-08-26 | Phillips Petroleum Company | Isomerization of unsaturated alcohols |
FR2597100A1 (fr) | 1986-01-21 | 1987-10-16 | Nippon Shinyaku Co Ltd | Derives du pyroglutamide |
DE3713127A1 (de) * | 1987-04-16 | 1988-11-03 | Consortium Elektrochem Ind | Verfahren zur herstellung von tiglinaldehyd |
JPH07103101B2 (ja) | 1989-07-24 | 1995-11-08 | キッセイ薬品工業株式会社 | ピログルタミン酸誘導体 |
ATE134624T1 (de) | 1990-02-19 | 1996-03-15 | Ciba Geigy Ag | Acylverbindungen |
US5273990A (en) | 1992-09-03 | 1993-12-28 | Ciba-Geigy Corporation | Phosphono substituted tetrazole derivatives |
US5250522A (en) | 1992-10-09 | 1993-10-05 | Ciba-Geigy Corporation | Phosphono/biaryl substituted amino acid derivatives |
EP0550313A1 (fr) | 1991-12-30 | 1993-07-07 | Synthelabo | Nouveaux dérivés de 2-(tétrazol-5-yl)-(1,1'-biphényle), leur préparation et leur utilisation comme intermédiaires de synthèse |
FR2688503B1 (fr) | 1992-03-16 | 1994-05-06 | Synthelabo | Procede de preparation de derives de 2-(tetrazol-5-yl)-[1,1'-biphenyle]. |
US5217996A (en) * | 1992-01-22 | 1993-06-08 | Ciba-Geigy Corporation | Biaryl substituted 4-amino-butyric acid amides |
US5412102A (en) | 1994-05-27 | 1995-05-02 | Syntex (U.S.A.) Inc. | Processes for preparing 1-butyl-2-[2'-(2H-tetrazol-5-yl) biphenyl-4-ylmethyl]-1H-indole-3-carboxylic acid |
US5550119A (en) | 1995-03-02 | 1996-08-27 | Ciba-Geigy Corporation | Phosphono substituted tetrazole derivatives as ECE inhibitors |
CA2246725A1 (en) | 1996-02-19 | 1997-08-21 | Japan Tobacco Inc. | Therapeutic agent for diabetes |
TW536540B (en) | 1997-01-30 | 2003-06-11 | Bristol Myers Squibb Co | Endothelin antagonists: N-[[2'-[[(4,5-dimethyl-3-isoxazolyl)amino]sulfonyl]-4-(2-oxazolyl)[1,1'-biphenyl]-2-yl]methyl]-N,3,3-trimethylbutanamide and N-(4,5-dimethyl-3-isoxazolyl)-2'-[(3,3-dimethyl-2-oxo-1-pyrrolidinyl)methyl]-4'-(2-oxazolyl)[1,1'-biphe |
DE69817974T2 (de) | 1997-11-14 | 2004-07-22 | Schering Ag | Ein Verfahren zur Herstellung von Pyrrolidinon-Derivaten |
CA2344412A1 (en) | 1998-09-21 | 2000-03-30 | Takeda Chemical Industries, Ltd. | Thiol compound, their production and use |
WO2001068591A1 (en) * | 2000-03-16 | 2001-09-20 | F. Hoffmann-La Roche Ag | Carboxylic acid derivatives as ip antagonists |
BRPI0306907B8 (pt) | 2002-01-17 | 2021-05-25 | Novartis Ag | composição farmacêutica, que compreende valsartan e inibidor de nep ou seus sais |
ATE473216T1 (de) | 2002-03-29 | 2010-07-15 | Senju Pharma Co | Hydroxymorpholinonderivat und dessen medizinische verwendung |
GB0402262D0 (en) | 2004-02-02 | 2004-03-10 | Novartis Ag | Process for the manufacture of organic compounds |
US7618981B2 (en) | 2004-05-06 | 2009-11-17 | Cytokinetics, Inc. | Imidazopyridinyl-benzamide anti-cancer agents |
WO2005108409A2 (en) | 2004-05-07 | 2005-11-17 | Umicore Ag & Co. Kg | Ferrocenyl ligands for homogeneous, enantioselective hydrogenation catalysts |
GB0418046D0 (en) | 2004-08-12 | 2004-09-15 | Prosidion Ltd | Eantioselective process |
MY146830A (en) | 2005-02-11 | 2012-09-28 | Novartis Ag | Combination of organic compounds |
EP1903027A1 (en) * | 2006-09-13 | 2008-03-26 | Novartis AG | Process for preparing biaryl substituted 4-amino-butyric acid or derivatives thereof and their use in the production of NEP inhibitors |
MY153432A (en) | 2007-01-12 | 2015-02-13 | Novartis Ag | Process for preparing 5-biphenyl-4-amino-2-methyl pentanoic acid |
ES2463693T3 (es) | 2007-05-10 | 2014-05-29 | R & D Biopharmaceuticals Gmbh | Derivados de tubulisina |
PE20091364A1 (es) * | 2008-01-17 | 2009-10-13 | Novartis Ag | Proceso para la preparacion de inhibidores de nep |
RU2564024C2 (ru) | 2010-01-22 | 2015-09-27 | Новартис Аг | Промежуточные продукты для получения ингибиторов нейтральной эндопептидазы и способ их получения |
WO2012025502A1 (en) | 2010-08-23 | 2012-03-01 | Novartis Ag | New process for the preparation of intermediates useful for the manufacture nep inhibitors |
-
2011
- 2011-08-22 KR KR1020137007279A patent/KR101476937B1/ko not_active IP Right Cessation
- 2011-08-22 MX MX2013002150A patent/MX2013002150A/es active IP Right Grant
- 2011-08-22 AU AU2011295170A patent/AU2011295170B2/en not_active Ceased
- 2011-08-22 BR BR112013004164A patent/BR112013004164A2/pt not_active IP Right Cessation
- 2011-08-22 EP EP11758421.9A patent/EP2609075B1/en active Active
- 2011-08-22 ES ES11758421.9T patent/ES2576179T3/es active Active
- 2011-08-22 PT PT117584219T patent/PT2609075E/pt unknown
- 2011-08-22 PL PL11758421.9T patent/PL2609075T3/pl unknown
- 2011-08-22 CA CA2806780A patent/CA2806780A1/en not_active Abandoned
- 2011-08-22 JP JP2013525279A patent/JP5705984B2/ja active Active
- 2011-08-22 RU RU2013112946/04A patent/RU2588572C2/ru not_active IP Right Cessation
- 2011-08-22 SI SI201130827A patent/SI2609075T1/sl unknown
- 2011-08-22 US US13/818,507 patent/US8835668B2/en active Active
- 2011-08-22 WO PCT/EP2011/064410 patent/WO2012025501A1/en active Application Filing
Also Published As
Publication number | Publication date |
---|---|
ES2576179T3 (es) | 2016-07-06 |
AU2011295170B2 (en) | 2014-12-18 |
US20130158285A1 (en) | 2013-06-20 |
JP5705984B2 (ja) | 2015-04-22 |
RU2588572C2 (ru) | 2016-07-10 |
EP2609075A1 (en) | 2013-07-03 |
AU2011295170A1 (en) | 2013-03-21 |
EP2609075B1 (en) | 2016-03-16 |
JP2013539462A (ja) | 2013-10-24 |
KR20130061735A (ko) | 2013-06-11 |
WO2012025501A1 (en) | 2012-03-01 |
PT2609075E (pt) | 2016-06-03 |
SI2609075T1 (sl) | 2016-06-30 |
US8835668B2 (en) | 2014-09-16 |
CA2806780A1 (en) | 2012-03-01 |
BR112013004164A2 (pt) | 2016-05-10 |
PL2609075T3 (pl) | 2016-09-30 |
RU2013112946A (ru) | 2014-09-27 |
KR101476937B1 (ko) | 2014-12-24 |
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Legal Events
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FG | Grant or registration |