MA30724B1 - Procede de preparation d'acide 4-amino-butyrique substitue par biaryle ou de derives de celui-ci et leur utilisation pour produire des inhibiteurs de nep. - Google Patents

Procede de preparation d'acide 4-amino-butyrique substitue par biaryle ou de derives de celui-ci et leur utilisation pour produire des inhibiteurs de nep.

Info

Publication number
MA30724B1
MA30724B1 MA31739A MA31739A MA30724B1 MA 30724 B1 MA30724 B1 MA 30724B1 MA 31739 A MA31739 A MA 31739A MA 31739 A MA31739 A MA 31739A MA 30724 B1 MA30724 B1 MA 30724B1
Authority
MA
Morocco
Prior art keywords
biaryl
derivatives
amino
substituted
producing
Prior art date
Application number
MA31739A
Other languages
English (en)
Inventor
David Hook
Bernhard Wietfeld
Matthias Lotz
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=37814152&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MA30724(B1) "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 MA30724B1 publication Critical patent/MA30724B1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C227/00—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C227/30—Preparation of optical isomers
    • C07C227/32—Preparation of optical isomers by stereospecific synthesis
    • 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
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • 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
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/22—Organic complexes
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C227/00—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C227/14—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton from compounds containing already amino and carboxyl groups or derivatives thereof
    • C07C227/16—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton from compounds containing already amino and carboxyl groups or derivatives thereof by reactions not involving the amino or carboxyl groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C229/02—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
    • C07C229/34—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton containing six-membered aromatic rings
    • 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
    • Y—GENERAL 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
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/50—Improvements relating to the production of bulk chemicals
    • Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Diabetes (AREA)
  • Engineering & Computer Science (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Emergency Medicine (AREA)
  • Endocrinology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • General Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Materials Engineering (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)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Catalysts (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Enzymes And Modification Thereof (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)

Abstract

LA PRÉSENTE INVENTION CONCERNE UN PROCÉDÉ DESTINÉ À PRODUIRE UN COMPOSÉ DE FORMULE (I) OU UN SEL DE CELUI-CI, FORMULE DANS LAQUELLE R1 ET R1´ SONT INDÉPENDAMMENT HYDROGÈNE OU UN GROUPE DE PROTECTION D'AMINE, ET R2 EST UN GROUPE CARBOXYLIQUE OU UN GROUPE ESTER. LE PROCÉDÉ CONSISTE À FAIRE RÉAGIR UN COMPOSÉ DE FORMULE (II) OU UN SEL DE CELUI-CI, FORMULE DANS LAQUELLE R1, R1´ ET R2 SONT TELS QUE DÉFINIS CI-DESSUS, AVEC DE L'HYDROGÈNE EN LA PRÉSENCE D'UN CATALYSEUR À MÉTAL DE TRANSITION ET D'UN LIGAND CHIRAL, LE MÉTAL DE TRANSITION ÉTANT CHOISI DANS LE GROUPE 7, 8 OU 9 DU TABLEAU PÉRIODIQUE DES ÉLÉMENTS. L'INVENTION CONCERNE ÉGALEMENT DES PRODUITS POUVANT ÊTRE OBTENUS PAR LEDIT PROCÉDÉ, ET LEUR UTILISATION POUR PRODUIRE DES INHIBITEURS DE NEP. L'INVENTION A ÉGALEMENT POUR OBJET L'UTILISATION DU CATALYSEUR À MÉTAL DE TRANSITION POUR PRÉPARER DES INHIBITEURS DE NEP OU DES PROMÉDICAMENTS DE CEUX-CI.
MA31739A 2006-09-13 2009-03-30 Procede de preparation d'acide 4-amino-butyrique substitue par biaryle ou de derives de celui-ci et leur utilisation pour produire des inhibiteurs de nep. MA30724B1 (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP06120576A EP1903027A1 (fr) 2006-09-13 2006-09-13 Procédé de préparation de l' acide amino-4 butyrique ou de ses derivés et leur utilisation pour la préparation des inhibiteurs NEP

Publications (1)

Publication Number Publication Date
MA30724B1 true MA30724B1 (fr) 2009-09-01

Family

ID=37814152

Family Applications (1)

Application Number Title Priority Date Filing Date
MA31739A MA30724B1 (fr) 2006-09-13 2009-03-30 Procede de preparation d'acide 4-amino-butyrique substitue par biaryle ou de derives de celui-ci et leur utilisation pour produire des inhibiteurs de nep.

Country Status (28)

Country Link
US (2) US20090326066A1 (fr)
EP (2) EP1903027A1 (fr)
JP (1) JP5455627B2 (fr)
KR (1) KR101401118B1 (fr)
CN (1) CN101516831B (fr)
AU (1) AU2007296889B2 (fr)
BR (1) BRPI0716990A2 (fr)
CA (1) CA2662393C (fr)
CO (1) CO6190550A2 (fr)
CY (1) CY1115696T1 (fr)
DK (1) DK2066618T3 (fr)
ES (1) ES2519446T3 (fr)
GT (1) GT200900058A (fr)
HR (1) HRP20140984T1 (fr)
IL (1) IL196925A (fr)
MA (1) MA30724B1 (fr)
MX (1) MX2009002746A (fr)
MY (1) MY146660A (fr)
NO (1) NO341967B1 (fr)
NZ (1) NZ574665A (fr)
PL (1) PL2066618T3 (fr)
PT (1) PT2066618E (fr)
RU (1) RU2469019C2 (fr)
SG (1) SG177205A1 (fr)
SI (1) SI2066618T1 (fr)
TN (1) TN2009000077A1 (fr)
WO (1) WO2008031567A1 (fr)
ZA (1) ZA200900779B (fr)

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PE20091364A1 (es) 2008-01-17 2009-10-13 Novartis Ag Proceso para la preparacion de inhibidores de nep
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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
JO2967B1 (en) 2009-11-20 2016-03-15 نوفارتس ايه جي Acetic acid derivatives of carbamoyl methyl amino are substituted as new NEP inhibitors
SI2526088T1 (sl) * 2010-01-22 2015-12-31 Novartis Ag Intermediati nevtralnih endopeptidaznih inhibitorjev in metoda za njihovo pripravo
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
ES2608780T3 (es) * 2010-08-23 2017-04-17 Novartis Ag Nuevo proceso para la preparación de intermediarios útiles para la elaboración de inhibidores de NEP
BR112013004164A2 (pt) 2010-08-23 2016-05-10 Novartis Ag processo para a preparação de intermediários para a produção de inibidores da nep
US8673974B2 (en) 2010-11-16 2014-03-18 Novartis Ag Substituted amino bisphenyl pentanoic acid derivatives as NEP inhibitors
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CN106977415B (zh) * 2016-01-15 2021-03-26 广东东阳光药业有限公司 一种沙库必曲的中间体及其制备方法
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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
JP6945619B2 (ja) 2016-08-17 2021-10-06 ノバルティス アーゲー Ｎｅｐ阻害剤合成のための新規な方法および中間体
CN106380421B (zh) * 2016-08-26 2017-12-08 中国科学院上海有机化学研究所 沙库必曲的合成方法
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CN106631903A (zh) * 2016-12-16 2017-05-10 重庆市碚圣医药科技股份有限公司 一种lcz‑696关键中间体的制备方法
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CN107522628A (zh) * 2017-09-20 2017-12-29 吉尔生化（上海）有限公司 一种l‑3‑（6‑乙酰基‑2‑萘胺基）‑2‑氨基丙酸的合成方法
CN108084058A (zh) * 2017-12-15 2018-05-29 江苏中邦制药有限公司 一种lcz696中间体的制备方法
CN108373423B (zh) * 2018-04-28 2020-10-23 成都苑东生物制药股份有限公司 一种沙库比曲缬沙坦复合物和/或共晶关键中间体沙库比曲钙的制备方法
CN109400504A (zh) * 2018-12-11 2019-03-01 重庆三圣实业股份有限公司 Lcz696中间体非对映异构体的分离纯化方法
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
CN111748590B (zh) * 2019-03-29 2024-05-28 弈柯莱(台州)药业有限公司 转氨酶在制备Sacubitril中间体中的应用
CN110128298B (zh) * 2019-06-13 2021-08-03 南京一心和医药科技有限公司 一种沙库巴曲中间体的合成方法
CN112574132B (zh) * 2019-09-30 2024-02-27 广东东阳光药业股份有限公司 一种沙库必曲缬沙坦钠的制备方法
CN113135836A (zh) * 2020-01-20 2021-07-20 鲁南制药集团股份有限公司 一种沙库巴曲钙盐的制备方法
CN113321600B (zh) * 2020-02-28 2024-06-14 四川科伦药物研究院有限公司 制备手性联芳基取代的4-氨基-丁酸及其衍生物的方法
CN113387841A (zh) * 2020-03-13 2021-09-14 凯特立斯（深圳）科技有限公司 一种沙库必曲中间体的合成方法
CN111269148B (zh) * 2020-04-08 2022-02-08 台州职业技术学院 一种沙库比曲中间体的制备方法
JP7064527B2 (ja) * 2020-05-01 2022-05-10 ノバルティス アーゲー サクビトリルカルシウム塩
CN112480179B (zh) * 2020-11-24 2025-11-14 苏州鹏旭医药科技有限公司 一种取代二茂铁基二膦均相催化剂配体
CN112745246A (zh) * 2020-12-30 2021-05-04 重庆市碚圣医药科技股份有限公司 一种沙库必曲中间体的纯化方法
CN119798080B (zh) * 2023-10-11 2025-10-03 杭州科巢生物科技有限公司 一种(r)-5-([1,1′-联苯基]-4-基)-2-甲基-4-氧代戊酸钙盐的制备方法
CN117924111A (zh) * 2023-12-14 2024-04-26 宣城美诺华药业有限公司 一种沙库巴曲缬沙坦钠的制备方法

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Also Published As

Publication number Publication date
SG177205A1 (en) 2012-01-30
RU2469019C2 (ru) 2012-12-10
CA2662393C (fr) 2015-11-03
RU2009113666A (ru) 2010-10-20
US8946481B2 (en) 2015-02-03
CO6190550A2 (es) 2010-08-19
EP2066618B1 (fr) 2014-07-23
EP1903027A1 (fr) 2008-03-26
AU2007296889A1 (en) 2008-03-20
WO2008031567A1 (fr) 2008-03-20
IL196925A (en) 2013-10-31
CY1115696T1 (el) 2017-01-25
AU2007296889B2 (en) 2012-03-01
EP2066618A1 (fr) 2009-06-10
HRP20140984T1 (hr) 2014-12-05
DK2066618T3 (da) 2014-09-22
MX2009002746A (es) 2009-03-26
BRPI0716990A2 (pt) 2014-02-04
TN2009000077A1 (en) 2010-08-19
PT2066618E (pt) 2014-09-10
NO20091242L (no) 2009-03-25
NZ574665A (en) 2012-03-30
US20090326066A1 (en) 2009-12-31
KR101401118B1 (ko) 2014-05-29
MY146660A (en) 2012-09-14
CN101516831B (zh) 2013-12-25
NO341967B1 (no) 2018-03-05
SI2066618T1 (sl) 2014-11-28
IL196925A0 (en) 2009-11-18
GT200900058A (es) 2010-03-11
JP2010503628A (ja) 2010-02-04
PL2066618T3 (pl) 2015-01-30
CN101516831A (zh) 2009-08-26
JP5455627B2 (ja) 2014-03-26
HK1131381A1 (en) 2010-01-22
US20130066101A1 (en) 2013-03-14
ES2519446T3 (es) 2014-11-07
KR20090076910A (ko) 2009-07-13
WO2008031567B1 (fr) 2008-05-08
CA2662393A1 (fr) 2008-03-20
ZA200900779B (en) 2009-12-30

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