PE20091364A1 - Proceso para la preparacion de inhibidores de nep - Google Patents
Proceso para la preparacion de inhibidores de nepInfo
- 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
Links
- 238000000034 method Methods 0.000 title abstract 3
- 239000003112 inhibitor Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 6
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract 2
- 102000003729 Neprilysin Human genes 0.000 abstract 2
- 108090000028 Neprilysin Proteins 0.000 abstract 2
- 229910052751 metal Inorganic materials 0.000 abstract 2
- 239000002184 metal Substances 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- -1 CARBOXYL Chemical group 0.000 abstract 1
- GPWHDDKQSYOYBF-UHFFFAOYSA-N ac1l2u0q Chemical group Br[Br-]Br GPWHDDKQSYOYBF-UHFFFAOYSA-N 0.000 abstract 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 abstract 1
- 150000001342 alkaline earth metals Chemical class 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 150000001450 anions Chemical class 0.000 abstract 1
- 150000007942 carboxylates Chemical group 0.000 abstract 1
- 150000004820 halides Chemical class 0.000 abstract 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 abstract 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 abstract 1
- 230000001681 protective effect Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic 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
- C07D207/30—Heterocyclic 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
- C07D207/34—Heterocyclic 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
- C07D207/36—Oxygen or sulfur atoms
- C07D207/38—2-Pyrrolones
-
- 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
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic 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
- C07D207/18—Heterocyclic 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
- C07D207/22—Heterocyclic 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
- C07D207/24—Oxygen or sulfur atoms
- C07D207/26—2-Pyrrolidones
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic 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
- C07D207/18—Heterocyclic 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
- C07D207/22—Heterocyclic 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
- C07D207/24—Oxygen or sulfur atoms
- C07D207/26—2-Pyrrolidones
- C07D207/263—2-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic 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
- C07D207/18—Heterocyclic 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
- C07D207/22—Heterocyclic 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
- C07D207/24—Oxygen or sulfur atoms
- C07D207/26—2-Pyrrolidones
- C07D207/263—2-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms
- C07D207/267—2-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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic 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
- C07D207/30—Heterocyclic 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
- C07D207/34—Heterocyclic 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
- C07D207/36—Oxygen or sulfur atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic 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
- C07D403/06—Heterocyclic 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
-
- 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
- C07C227/22—Preparation 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
-
- 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
-
- 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)
- 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)
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) | NZ600119A (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 (52)
| 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 |
| WO2011035569A1 (en) | 2009-09-23 | 2011-03-31 | Zhejiang Jiuzhou Pharmaceutical Co., Ltd. | Process for manufacture of n-acylbphenyl alanine |
| US8450496B2 (en) * | 2009-03-24 | 2013-05-28 | Hoffman-La Roche Inc. | Process for the preparation of propionic acid derivatives |
| ES2523734T3 (es) | 2009-05-28 | 2014-12-01 | Novartis Ag | Derivados aminopropiónicos sustituidos como inhibidores de neprilisina |
| JP5466759B2 (ja) | 2009-05-28 | 2014-04-09 | ノバルティス アーゲー | ネプリライシン阻害剤としての置換アミノ酪酸誘導体 |
| JO2967B1 (en) | 2009-11-20 | 2016-03-15 | نوفارتس ايه جي | Acetic acid derivatives of carbamoyl methyl amino are substituted as new NEP inhibitors |
| CN102712585B (zh) * | 2010-01-22 | 2015-06-24 | 诺华股份有限公司 | 中性内肽酶抑制剂中间体和其制备方法 |
| 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 |
| JP6002133B2 (ja) * | 2010-08-23 | 2016-10-05 | ノバルティス アーゲー | Nep阻害剤の製造に有用な中間体の新規調製方法 |
| EP2609075B1 (en) * | 2010-08-23 | 2016-03-16 | Novartis AG | Process for the preparation of intermediates for the manufacture of nep inhibitors |
| US8673974B2 (en) | 2010-11-16 | 2014-03-18 | Novartis Ag | Substituted amino bisphenyl pentanoic acid derivatives as NEP inhibitors |
| ME02295B (me) | 2010-12-15 | 2016-02-20 | Theravance Biopharma R&D Ip Llc | Inhibitori neprilizina |
| CN103261168B (zh) | 2010-12-15 | 2015-08-05 | 施万生物制药研发Ip有限责任公司 | 脑啡肽酶抑制剂 |
| SG192815A1 (en) | 2011-02-17 | 2013-09-30 | Theravance Inc | Substituted aminobutyric derivatives as neprilysin inhibitors |
| WO2012154249A1 (en) | 2011-02-17 | 2012-11-15 | Theravance, Inc. | Substituted aminobutyric derivatives as neprilysin inhibitors |
| WO2012166389A1 (en) | 2011-05-31 | 2012-12-06 | Theravance, Inc. | Neprilysin inhibitors |
| EP2714662B1 (en) | 2011-05-31 | 2017-10-11 | Theravance Biopharma R&D IP, LLC | Neprilysin inhibitors |
| JP5959075B2 (ja) | 2011-05-31 | 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 |
| 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 |
| US8871792B2 (en) | 2012-06-08 | 2014-10-28 | Theravance Biopharma R&D Ip, Llc | Neprilysin inhibitors |
| SG11201408094YA (en) | 2012-06-08 | 2015-01-29 | Theravance Biopharma R & D Ip Llc | Neprilysin inhibitors |
| HUE031301T2 (hu) | 2012-08-08 | 2017-07-28 | Theravance Biopharma R&D Ip Llc | Neprilizin inhibitorok |
| JP6301371B2 (ja) | 2013-02-14 | 2018-04-11 | ノバルティス アーゲー | インビボ効力が改善されたnep阻害剤としての置換ビスフェニルブタン酸誘導体 |
| MX367525B (es) | 2013-02-14 | 2019-08-26 | Novartis Ag | Derivados de ácido bisfenil-butanoico fosfónico sustituido como inhibidores de la endopeptidasa neutra (nep). |
| SMT201700368T1 (it) | 2013-03-05 | 2017-09-07 | Theravance Biopharma R&D Ip Llc | Inibitori di neprilisina |
| ES2765511T3 (es) * | 2013-11-15 | 2020-06-09 | Hoffmann La Roche | Procesos para la preparación de compuestos de pirimidinilciclopentano |
| WO2015116786A1 (en) | 2014-01-30 | 2015-08-06 | Theravance Biopharma R&D Ip, Llc | Neprilysin inhibitors |
| CN105960398A (zh) | 2014-01-30 | 2016-09-21 | 施万生物制药研发Ip有限责任公司 | 5-联苯-4-杂芳基羰基氨基-戊酸衍生物作为脑啡肽酶抑制剂 |
| EP3218351B1 (en) | 2014-11-14 | 2019-06-19 | Zentiva K.S. | A method for the preparation, isolation and purification of pharmaceutically applicable forms of ahu-377 |
| WO2016097242A1 (de) * | 2014-12-19 | 2016-06-23 | Basf Se | Verfahren zur herstellung optisch aktiver carbonylverbindungen |
| US9433598B2 (en) | 2015-02-11 | 2016-09-06 | Theravance Biopharma R&D Ip, Llc | (2S,4R)-5-(5′-chloro-2′-fluorobiphenyl-4-yl)-4-(ethoxyoxalylamino)-2-hydroxymethyl-2-methylpentanoic acid |
| TW201632493A (zh) | 2015-02-13 | 2016-09-16 | 諾華公司 | 新穎方法 |
| HRP20210040T1 (hr) | 2015-02-19 | 2021-04-02 | Theravance Biopharma R&D Ip, Llc | (2r,4r)-5-(5′-klor-2’-fluorbifenil-4-il)-2-hidroksi-4-[(5-metiloksazol-2-karbonil)amino]pentanska kiselina |
| 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 |
| KR102763706B1 (ko) | 2015-12-10 | 2025-02-07 | 노파르티스 아게 | 신규 방법 및 중간체 |
| 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. |
| RS62172B1 (sr) | 2016-03-08 | 2021-08-31 | Theravance Biopharma R&D Ip Llc | Kristalna (2s,4r)-5-(5’-hloro-2-fluoro-[1,1’-bifenil]-4-il)-2-(etoksimetil)-4-(3-hidroksi izoksazol-5-karboksamido)-2-metilpentanska kiselina i njene upotrebe |
| JP6944473B2 (ja) | 2016-07-05 | 2021-10-06 | 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 |
| US10851059B2 (en) | 2016-08-17 | 2020-12-01 | Novartis Ag | Processes and intermediates for NEP inhibitor synthesis |
| WO2018116203A1 (en) | 2016-12-23 | 2018-06-28 | Novartis Ag | New process for early sacubitril intermediates |
| 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 |
| CN117510376A (zh) * | 2023-10-17 | 2024-02-06 | 四川新迪生物制药有限公司 | 一种手性联芳基取代的4-氨基-丁酸及其衍生物的制备方法 |
| WO2025164594A1 (ja) * | 2024-01-29 | 2025-08-07 | 高砂香料工業株式会社 | ルテニウム-ジホスフィン-カルボキシラート錯体及びその製造方法 |
| CN118239990B (zh) * | 2024-05-28 | 2025-03-14 | 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)
| 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 |
| FR2688503B1 (fr) | 1992-03-16 | 1994-05-06 | Synthelabo | Procede de preparation de derives de 2-(tetrazol-5-yl)-[1,1'-biphenyle]. |
| 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 |
| 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 |
| TWI413638B (zh) * | 2007-01-12 | 2013-11-01 | Novartis Ag | 新穎方法 |
| US8980833B2 (en) | 2007-05-10 | 2015-03-17 | R&D-Biopharmaceuticals Gmbh | Tubulysine derivatives |
| PE20091364A1 (es) * | 2008-01-17 | 2009-10-13 | Novartis Ag | Proceso para la preparacion de inhibidores de nep |
| CN102712585B (zh) * | 2010-01-22 | 2015-06-24 | 诺华股份有限公司 | 中性内肽酶抑制剂中间体和其制备方法 |
| EP2609075B1 (en) * | 2010-08-23 | 2016-03-16 | Novartis AG | Process for the preparation of intermediates for the manufacture of nep inhibitors |
| JP6002133B2 (ja) * | 2010-08-23 | 2016-10-05 | ノバルティス アーゲー | Nep阻害剤の製造に有用な中間体の新規調製方法 |
-
2009
- 2009-01-15 PE PE2009000047A patent/PE20091364A1/es not_active Application Discontinuation
- 2009-01-15 AR ARP090100121A patent/AR070176A1/es unknown
- 2009-01-16 JP JP2010544498A patent/JP5739667B2/ja active Active
- 2009-01-16 CN CN2009801061724A patent/CN101952249B/zh active Active
- 2009-01-16 ES ES09702021.8T patent/ES2602564T3/es active Active
- 2009-01-16 AU AU2009204759A patent/AU2009204759B2/en not_active Ceased
- 2009-01-16 CL CL2009000089A patent/CL2009000089A1/es unknown
- 2009-01-16 CN CN201310143383.3A patent/CN103483236B/zh active Active
- 2009-01-16 NZ NZ600119A patent/NZ600119A/xx not_active IP Right Cessation
- 2009-01-16 MY MYPI2010003112A patent/MY169425A/en unknown
- 2009-01-16 US US12/863,213 patent/US8580974B2/en active Active
- 2009-01-16 TW TW098101721A patent/TWI422370B/zh not_active IP Right Cessation
- 2009-01-16 EP EP09702021.8A patent/EP2245009B1/en active Active
- 2009-01-16 PL PL09702021T patent/PL2245009T3/pl unknown
- 2009-01-16 SG SG2013004098A patent/SG187491A1/en unknown
- 2009-01-16 HU HUE09702021A patent/HUE030606T2/en unknown
- 2009-01-16 RU RU2010133903/04A patent/RU2513521C2/ru not_active IP Right Cessation
- 2009-01-16 CA CA2711529A patent/CA2711529C/en not_active Expired - Fee Related
- 2009-01-16 MX MX2010007842A patent/MX2010007842A/es active IP Right Grant
- 2009-01-16 BR BRPI0906764-7A patent/BRPI0906764A2/pt not_active IP Right Cessation
- 2009-01-16 WO PCT/EP2009/050510 patent/WO2009090251A2/en not_active Ceased
- 2009-01-16 NZ NZ586657A patent/NZ586657A/en not_active IP Right Cessation
- 2009-01-16 KR KR1020107018152A patent/KR101587668B1/ko not_active Expired - Fee Related
- 2009-01-16 PT PT97020218T patent/PT2245009T/pt unknown
- 2009-01-16 SI SI200931552A patent/SI2245009T1/sl unknown
-
2010
- 2010-06-28 IL IL206664A patent/IL206664A0/en unknown
- 2010-06-30 MA MA32970A patent/MA31951B1/fr unknown
- 2010-06-30 TN TN2010000304A patent/TN2010000304A1/fr unknown
- 2010-07-16 GT GT201000211A patent/GT201000211A/es unknown
- 2010-08-12 CO CO10099278A patent/CO6290677A2/es active IP Right Grant
- 2010-08-17 EC EC2010010405A patent/ECSP10010405A/es unknown
-
2013
- 2013-10-31 RU RU2013148670A patent/RU2636936C2/ru not_active IP Right Cessation
- 2013-11-06 JP JP2013230570A patent/JP5800882B2/ja active Active
- 2013-11-11 US US14/076,302 patent/US9061973B2/en active Active
-
2015
- 2015-05-18 US US14/715,129 patent/US9227934B2/en active Active
- 2015-11-12 US US14/939,513 patent/US9403766B2/en active Active
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| PE20091364A1 (es) | Proceso para la preparacion de inhibidores de nep | |
| BR112012018408A2 (pt) | composição do combustível diesel, pacote do aditivo, uso de um aditivo e uso de uma composição do combustível diesel. | |
| AR081385A1 (es) | Composiciones metodo y uso | |
| PH12016502037A1 (en) | Certain amino-pyrimidines, compositions thereof, and methods for their use | |
| PH12017501192B1 (en) | Certain amino-pyridazines, compositions thereof, and methods of their use | |
| AR079205A1 (es) | Morfolinotiazoles como moduladores alostericos positivos alfa 7 | |
| 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 | |
| ECSP21016009A (es) | Inhibidores de sarcómeros cardíacos | |
| UY33357A (es) | Uracilos herbicidas | |
| PE20050088A1 (es) | Proceso para la fabricacion de valsartan | |
| BR112012024403A2 (pt) | processo de preparo de derivados de amino-benzofurano | |
| MX2019006766A (es) | Aditivos para combustibles de amonio cuaternario. | |
| MX2014011752A (es) | Compuestos heterobiciclicos n-sustituidos y derivados para combatir plagas de animales ii. | |
| MX2014002106A (es) | Composicion ionomerica antimicrobiana y usos de la misma. | |
| MX2016005829A (es) | Procedimiento para la preparacion de iopamidol. | |
| PE20090956A1 (es) | PROCESO PARA LA OBTENCION DE DERIVADOS DE PIRIDO [2,1-a] - ISOQUINOLINA | |
| AR072880A1 (es) | Derivados nitrogenados de la pancratistatina | |
| AR098484A1 (es) | Insecticidas de 1-aril-3-alquilpirazol | |
| 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 | |
| MX344516B (es) | Bifenoles halogenados como agentes antibacterianos. | |
| CL2008003086A1 (es) | Proceso para preparar 2-(fenilo sustituido-2-hidroxi-etil) carbamatos por reduccion de un alfa-alcohol ester protegido. | |
| 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 |