Nothing Special   »   [go: up one dir, main page]

PE20091364A1 - Proceso para la preparacion de inhibidores de nep - Google Patents

Proceso para la preparacion de inhibidores de nep

Info

Publication number
PE20091364A1
PE20091364A1 PE2009000047A PE2009000047A PE20091364A1 PE 20091364 A1 PE20091364 A1 PE 20091364A1 PE 2009000047 A PE2009000047 A PE 2009000047A PE 2009000047 A PE2009000047 A PE 2009000047A PE 20091364 A1 PE20091364 A1 PE 20091364A1
Authority
PE
Peru
Prior art keywords
formula
compound
preparation
alkaline
ammonium
Prior art date
Application number
PE2009000047A
Other languages
English (en)
Inventor
David Hook
Daniel Kaufmann
Erhard Bappert
Philippe Polleux
Bernhard Riss
Matthias Napp
Jonathan Medlock
Antonio Zanotti-Gerosa
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 PE20091364A1 publication Critical patent/PE20091364A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/30Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
    • C07D207/34Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D207/36Oxygen or sulfur atoms
    • C07D207/382-Pyrrolones
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/12Drugs for disorders of the urinary system of the kidneys
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/10Antioedematous agents; Diuretics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/04Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/12Antihypertensives
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/18Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom 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
    • C07D207/22Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D207/24Oxygen or sulfur atoms
    • C07D207/262-Pyrrolidones
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/18Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom 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
    • C07D207/22Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D207/24Oxygen or sulfur atoms
    • C07D207/262-Pyrrolidones
    • C07D207/2632-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/18Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom 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
    • C07D207/22Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D207/24Oxygen or sulfur atoms
    • C07D207/262-Pyrrolidones
    • C07D207/2632-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms
    • C07D207/2672-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to the ring nitrogen atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/30Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
    • C07D207/34Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D207/36Oxygen or sulfur atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/06Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C227/00Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C227/22Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton from lactams, cyclic ketones or cyclic oximes, e.g. by reactions involving Beckmann rearrangement
    • 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
    • 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)
  • 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)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Hospice & Palliative Care (AREA)
  • Urology & Nephrology (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pyrrole Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

SE REFIERE A UN PROCESO PARA LA PREPARACION DE UN COMPUESTO DE FORMULA (7) DONDE R1 ES H O UN GRUPO PROTECTOR DE N; R6 Y R7 SON CADA UNO ALQUILO, ARILO, ARIL-ALQUILO, CICLOALQUILO, ENTRE OTROS; EN DONDE DICHO PROCESO COMPRENDE: A) HACER REACCIONAR UN COMPUESTO DE FORMULA (8) i) CON UNA AMINA DE FORMULA (13), (14) O (15) Y OPCIONALMENTE UNA SAL DE METAL ALCALINO, DE AMONIO, ENTRE OTROS; ii) CON UN COMPUESTO PREPARADO CON LA MEZCLA DE UN COMPUESTO DE FORMULA (18) CON UN ALCOHOLATO DE FORMULA M-O-R8 Y OPCIONALMENTE TRATADO CON UNA SAL M1X'; O iii) CON MEZCLAS DE LOS MISMOS; EN DONDE R8 ES CARBOXILATO O TRIBROMURO; X Y X' SON CADA UNO UN ANION TAL COMO HALURO, PERCLORATO, ENTRE OTROS; M ES UN METAL ALCALINO O ALCALINOTERREO; M1 ES UN METAL ALCALINO, AMONIO, ENTRE OTROS. DICHOS COMPUESTOS SON INTERMEDIARIOS PARA LA PREPARACION DE UN COMPUESTO DE FORMULA (1) DONDE R3 ES CARBOXILO O ESTER, QUE INHIBEN LA ENDOPEPTIDASA NEUTRA (NEP)
PE2009000047A 2008-01-17 2009-01-15 Proceso para la preparacion de inhibidores de nep PE20091364A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP08150353 2008-01-17

Publications (1)

Publication Number Publication Date
PE20091364A1 true PE20091364A1 (es) 2009-10-13

Family

ID=40758693

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2009000047A PE20091364A1 (es) 2008-01-17 2009-01-15 Proceso para la preparacion de inhibidores de nep

Country Status (29)

Country Link
US (4) US8580974B2 (es)
EP (1) EP2245009B1 (es)
JP (2) JP5739667B2 (es)
KR (1) KR101587668B1 (es)
CN (2) CN101952249B (es)
AR (1) AR070176A1 (es)
AU (1) AU2009204759B2 (es)
BR (1) BRPI0906764A2 (es)
CA (1) CA2711529C (es)
CL (1) CL2009000089A1 (es)
CO (1) CO6290677A2 (es)
EC (1) ECSP10010405A (es)
ES (1) ES2602564T3 (es)
GT (1) GT201000211A (es)
HU (1) HUE030606T2 (es)
IL (1) IL206664A0 (es)
MA (1) MA31951B1 (es)
MX (1) MX2010007842A (es)
MY (1) MY169425A (es)
NZ (2) NZ586657A (es)
PE (1) PE20091364A1 (es)
PL (1) PL2245009T3 (es)
PT (1) PT2245009T (es)
RU (2) RU2513521C2 (es)
SG (1) SG187491A1 (es)
SI (1) SI2245009T1 (es)
TN (1) TN2010000304A1 (es)
TW (1) TWI422370B (es)
WO (1) WO2009090251A2 (es)

Families Citing this family (50)

* Cited by examiner, † Cited by third party
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
US8450496B2 (en) * 2009-03-24 2013-05-28 Hoffman-La Roche Inc. Process for the preparation of propionic acid derivatives
EP2435402B1 (en) 2009-05-28 2016-04-13 Novartis AG Substituted aminobutyric derivatives as neprilysin inhibitors
JP5420761B2 (ja) 2009-05-28 2014-02-19 ノバルティス アーゲー ネプリリシン阻害剤としての置換アミノプロピオン酸誘導体
RU2534619C2 (ru) 2009-09-23 2014-11-27 Чжэцзян Цзючжоу Фармасьютикл Ко., Лтд. Способ получения n-ацилбифенилаланина
JO2967B1 (en) 2009-11-20 2016-03-15 نوفارتس ايه جي Acetic acid derivatives of carbamoyl methyl amino are substituted as new NEP inhibitors
US9067883B2 (en) * 2010-01-22 2015-06-30 Novartis Ag Intermediates of neutral endopeptidase inhibitors and preparation method thereof
WO2012025502A1 (en) 2010-08-23 2012-03-01 Novartis Ag New process for the preparation of intermediates useful for the manufacture nep inhibitors
CN103080077B (zh) * 2010-08-23 2015-06-10 诺华股份有限公司 用于制造nep抑制剂的中间体的制备工艺
SI2609075T1 (sl) * 2010-08-23 2016-06-30 Novartis Ag Postopek za pripravo intermediatov za izdelavo NEP inhibitorjev
US8673974B2 (en) 2010-11-16 2014-03-18 Novartis Ag Substituted amino bisphenyl pentanoic acid derivatives as NEP inhibitors
EP2651900B1 (en) 2010-12-15 2015-08-19 Theravance Biopharma R&D IP, LLC Neprilysin inhibitors
NZ610983A (en) 2010-12-15 2014-10-31 Theravance Biopharma R & D Ip Llc Neprilysin inhibitors
JP5959066B2 (ja) 2011-02-17 2016-08-02 セラヴァンス バイオファーマ アール&ディー アイピー, エルエルシー ネプリライシン阻害剤としての置換アミノ酪酸誘導体
MX342212B (es) 2011-02-17 2016-09-20 Theravance Inc Inhibidores de neprilisina.
CA2835220A1 (en) 2011-05-31 2012-12-06 Theravance, Inc. Neprilysin inhibitors
US8513244B2 (en) 2011-05-31 2013-08-20 Theravance, Inc. Neprilysin inhibitors
JP5885832B2 (ja) 2011-05-31 2016-03-16 セラヴァンス バイオファーマ アール&ディー アイピー, エルエルシー ネプリライシン阻害剤
TWI560172B (en) 2011-11-02 2016-12-01 Theravance Biopharma R&D Ip Llc Neprilysin inhibitors
CN104350052B (zh) 2012-05-31 2017-05-31 施万生物制药研发Ip有限责任公司 一氧化氮供体脑啡肽酶抑制剂
CN104470521B (zh) 2012-06-08 2017-04-12 施万生物制药研发Ip有限责任公司 脑啡肽酶抑制剂
LT2864292T (lt) 2012-06-08 2017-07-10 Theravance Biopharma R&D Ip, Llc Neprilizino inhibitoriai
BR112015002821B1 (pt) 2012-08-08 2022-10-18 Theravance Biopharma R&D Ip, Llc Compostos inibidores de neprilisina e composição farmacêutica
PL2956464T3 (pl) 2013-02-14 2018-08-31 Novartis Ag Podstawione pochodne bisfenylowe kwasu butanowofosfonowego jako inhibitory nep (neutralnej endopeptydazy)
EP2956445A1 (en) 2013-02-14 2015-12-23 Novartis AG Substituted bisphenyl butanoic acid derivatives as nep inhibitors with improved in vivo efficacy
PT2964616T (pt) 2013-03-05 2017-08-08 Theravance Biopharma R&D Ip Llc Inibidores da neprilisina
ES2957314T3 (es) * 2013-11-15 2024-01-17 Hoffmann La Roche Procesos para la preparación de compuestos de pirimidinilciclopentano
AU2015210983B2 (en) 2014-01-30 2018-10-04 Theravance Biopharma R&D Ip, Llc Neprilysin inhibitors
SG11201606057PA (en) 2014-01-30 2016-08-30 Theravance Biopharma R&D Ip Llc 5-biphenyl-4-heteroarylcarbonylamino-pentanoic acid derivatives as neprilysin inhibitors
PT3218351T (pt) 2014-11-14 2019-09-26 Zentiva Ks Um método para a preparação, isolamento e purificação de formas farmaceuticamente aplicáveis de ahu-377
CN107250091B (zh) * 2014-12-19 2021-05-04 巴斯夫欧洲公司 合成光学活性羰基化合物的方法
CA2974741C (en) 2015-02-11 2022-10-18 Theravance Biopharma R&D Ip, Llc (2s,4r)-5-(5'-chloro-2'-fluorobiphenyl-4-yl)-4-(ethoxyoxalylamino)-2-hydroxymethyl-2-methylpentanoic acid as neprilysin inhibitor
TW201632493A (zh) 2015-02-13 2016-09-16 諾華公司 新穎方法
AU2016220348B2 (en) 2015-02-19 2019-10-17 Theravance Biopharma R&D Ip, Llc (2R,4R)-5-(5'-chloro-2'-fluorobiphenyl-4-yl)-2-hydroxy-4-[(5-methyloxazole-2-carbonyl)amino]pentanoic acid
CN106146351B (zh) * 2015-04-03 2020-09-11 博瑞生物医药(苏州)股份有限公司 制备联芳基取代的4-氨基-丁酸或其衍生物的方法
CN105061263B (zh) * 2015-08-11 2017-03-15 苏州楚凯药业有限公司 一种nep抑制剂中间体的制备方法
CN105152980B (zh) * 2015-09-11 2017-03-29 浙江永宁药业股份有限公司 N‑叔丁氧羰基‑(4s)‑(对苯基苯基甲基)‑4‑氨基‑(2r)‑甲基丁酸的手性制备方法
WO2017051326A1 (en) 2015-09-23 2017-03-30 Novartis Ag New processes and intermediates useful in synthesis of nep inhibitors
WO2017098430A1 (en) 2015-12-10 2017-06-15 Novartis Ag New process and intermediates
EP3386945A1 (en) 2015-12-11 2018-10-17 Zentiva, K.S. Solid forms of (2r,4s)-5-(biphenyl-4-yl)-4-[(3-carboxypropionyl)amino]-2- -methylpentanoic acid ethyl ester, its salts and a preparation method
RU2756223C2 (ru) 2016-03-08 2021-09-28 ТЕРЕВАНС БАЙОФАРМА Ар энд Ди АйПи, ЭлЭлСи Кристаллическая (2s,4r)-5-(5'-хлор-2'-фтор-[1,1'-бифенил]-4-ил)-2-(этоксиметил)-4-(3-гидроксиизоксазол-5-карбоксамидо)-2-метилпентановая кислота и ее применения
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
EP3421455B1 (en) * 2017-06-29 2019-03-27 F.I.S.- Fabbrica Italiana Sintetici S.p.A. Improved process for the preparation of chiral 3-amino-piperidins, useful intermediates for the preparation of tofacitinib
CN109912508B (zh) * 2019-04-30 2022-08-12 上海天慈国际药业有限公司 一种右美托咪定及其盐酸盐的制备方法
CN110878039A (zh) * 2019-12-18 2020-03-13 株洲千金药业股份有限公司 一种沙库巴曲缬沙坦钠杂质的制备方法
CN115611857B (zh) * 2022-09-09 2024-05-31 上海伍夫科技有限公司 一种2-甲基-5-(1-甲基吡咯烷-2-基)吡啶的制备方法
CN115772088A (zh) * 2022-12-28 2023-03-10 海门瑞一医药科技有限公司 一种叔丁氧基(双二甲胺基)甲烷的制备方法
CN118239990A (zh) * 2024-05-28 2024-06-25 北京元延医药科技股份有限公司 不对称氢化催化合成药物的稀有贵金属和手性膦的配合物

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3164237D1 (en) 1980-12-23 1984-07-19 Air Ind Thermo-electrical plants
US5250552A (en) * 1991-05-09 1993-10-05 Warner-Lambert Company 3-[thiazolidinone, oxazolidinone, imidazolidinone]-indoles as antiinflammatory agents
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
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
GB0402262D0 (en) 2004-02-02 2004-03-10 Novartis Ag Process for the manufacture of organic compounds
AR057882A1 (es) * 2005-11-09 2007-12-26 Novartis Ag Compuestos de accion doble de bloqueadores del receptor de angiotensina e inhibidores de endopeptidasa neutra
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
EP2121578B1 (en) * 2007-01-12 2016-08-10 Novartis AG Process for preparing 5-biphenyl-4-amino-2-methyl pentanoic acid
EP2532673A3 (en) 2007-05-10 2014-01-08 R & D Biopharmaceuticals Gmbh Tubulysine derivatives
PE20091364A1 (es) * 2008-01-17 2009-10-13 Novartis Ag Proceso para la preparacion de inhibidores de nep
US9067883B2 (en) * 2010-01-22 2015-06-30 Novartis Ag Intermediates of neutral endopeptidase inhibitors and preparation method thereof
SI2609075T1 (sl) * 2010-08-23 2016-06-30 Novartis Ag Postopek za pripravo intermediatov za izdelavo NEP inhibitorjev
WO2012025502A1 (en) * 2010-08-23 2012-03-01 Novartis Ag New process for the preparation of intermediates useful for the manufacture nep inhibitors

Also Published As

Publication number Publication date
SI2245009T1 (sl) 2016-12-30
CN103483236A (zh) 2014-01-01
WO2009090251A3 (en) 2009-12-23
IL206664A0 (en) 2010-12-30
ES2602564T3 (es) 2017-02-21
TN2010000304A1 (en) 2011-11-11
US9061973B2 (en) 2015-06-23
JP2014070076A (ja) 2014-04-21
CA2711529A1 (en) 2009-07-23
WO2009090251A2 (en) 2009-07-23
PL2245009T3 (pl) 2017-06-30
NZ586657A (en) 2012-06-29
RU2513521C2 (ru) 2014-04-20
US20150246881A1 (en) 2015-09-03
MA31951B1 (fr) 2010-12-01
US20140243546A1 (en) 2014-08-28
AR070176A1 (es) 2010-03-17
TWI422370B (zh) 2014-01-11
TW200938188A (en) 2009-09-16
NZ600119A (en) 2013-07-26
RU2010133903A (ru) 2012-02-27
EP2245009B1 (en) 2016-08-10
KR101587668B1 (ko) 2016-01-22
US9227934B2 (en) 2016-01-05
CN101952249A (zh) 2011-01-19
MX2010007842A (es) 2010-08-09
BRPI0906764A2 (pt) 2015-08-18
CO6290677A2 (es) 2011-06-20
AU2009204759B2 (en) 2012-06-07
CL2009000089A1 (es) 2010-01-22
KR20100119867A (ko) 2010-11-11
MY169425A (en) 2019-04-04
SG187491A1 (en) 2013-02-28
RU2013148670A (ru) 2015-05-10
US20110046397A1 (en) 2011-02-24
CA2711529C (en) 2016-11-22
GT201000211A (es) 2014-03-14
JP2011510097A (ja) 2011-03-31
JP5800882B2 (ja) 2015-10-28
JP5739667B2 (ja) 2015-06-24
US20160060217A1 (en) 2016-03-03
PT2245009T (pt) 2016-11-10
EP2245009A2 (en) 2010-11-03
US9403766B2 (en) 2016-08-02
CN103483236B (zh) 2016-09-28
ECSP10010405A (es) 2010-09-30
CN101952249B (zh) 2013-10-16
US8580974B2 (en) 2013-11-12
AU2009204759A1 (en) 2009-07-23
RU2636936C2 (ru) 2017-11-29
HUE030606T2 (en) 2017-05-29

Similar Documents

Publication Publication Date Title
PE20091364A1 (es) Proceso para la preparacion de inhibidores de nep
MX2012009076A (es) Composiciones de combustible.
AR081385A1 (es) Composiciones metodo y uso
PH12012502096B1 (en) Certain amino-pyrimidines, compositions thereof, and methods for their use
AR079205A1 (es) Morfolinotiazoles como moduladores alostericos positivos alfa 7
MX343264B (es) Ciertas amino-piridazinas, composiciones de las mismas y metodos de uso de los mismos.
AR048669A1 (es) Derivados biciclicos de bisamida
CR20190244A (es) Agentes control de plaga
PE20040956A1 (es) Procedimiento para preparar la sal 5-[(r)-2-(5,6-dietil-indan-2-ilamino)-1-hidroxi-etil]-8-hidroxi-(1h)-quinolin-2-ona
UY33357A (es) Uracilos herbicidas
PE20050088A1 (es) Proceso para la fabricacion de valsartan
ECSP21016009A (es) Inhibidores de sarcómeros cardíacos
BR112012024403A2 (pt) processo de preparo de derivados de amino-benzofurano
BR112012021198A2 (pt) composto de pirazolopirimidina e seu uso como inibidores de pde10
PE20141040A1 (es) Composicion farmaceutica que comprende un derivado de amida que inhibe el crecimiento de celulas con cancer y lubricante de sal no metalica
AR079662A1 (es) Indolil-piperidinil bencilaminas como inhibidores de beta-triptasa
PE20090956A1 (es) PROCESO PARA LA OBTENCION DE DERIVADOS DE PIRIDO [2,1-a] - ISOQUINOLINA
PE20091359A1 (es) Proceso de preparacion de compuestos organicos intermediarios de inhibidores de renina
BR112013010850A2 (pt) composto de etinilfenilamidina ou sal do mesmo, método para produzir o mesmo e fungicida para uso agrícola e em horticultura
UY32246A (es) Derivados de carbamatos de alquil-heterociclos, su preparación y su aplicación en terapéutica
AR072880A1 (es) Derivados nitrogenados de la pancratistatina
CO6290758A2 (es) Proceso para la elaboracion de [fenilsulfanilfenil]piperidinas
PE20142331A1 (es) Metodo para preparar un compuesto mediante la reaccion de adicion de michael novedosa usando agua o varios acidos como aditivo
MX2015017864A (es) Metodo de preparacion de derivados de acido pirrolidina-2-carboxil ico.
BR9809473A (pt) Mistura fungida, e, processo para controlar fungos nocivos

Legal Events

Date Code Title Description
FG Grant, registration
FD Application declared void or lapsed