MX2009002121A - Proceso para la manufactura del acido n-(8-[2-hidroxibenzoil]-amin o)caprilico. - Google Patents

Proceso para la manufactura del acido n-(8-[2-hidroxibenzoil]-amin o)caprilico.

Info

Publication number
MX2009002121A
MX2009002121A MX2009002121A MX2009002121A MX2009002121A MX 2009002121 A MX2009002121 A MX 2009002121A MX 2009002121 A MX2009002121 A MX 2009002121A MX 2009002121 A MX2009002121 A MX 2009002121A MX 2009002121 A MX2009002121 A MX 2009002121A
Authority
MX
Mexico
Prior art keywords
snac
manufacture
hydroxybenzoyl
amino
formation
Prior art date
Application number
MX2009002121A
Other languages
English (en)
Inventor
William Elliott Bay
Yi Ren
Pingsheng Zhang
Joseph Norman Bernadino
George Frederick Klein
Original Assignee
Hoffmann La Roche
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 Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of MX2009002121A publication Critical patent/MX2009002121A/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C231/00Preparation of carboxylic acid amides
    • C07C231/10Preparation of carboxylic acid amides from compounds not provided for in groups C07C231/02 - C07C231/08
    • 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
    • C07C231/00Preparation of carboxylic acid amides
    • C07C231/22Separation; Purification; Stabilisation; Use of additives
    • C07C231/24Separation; Purification
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C235/00Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
    • C07C235/42Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton
    • C07C235/44Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton with carbon atoms of carboxamide groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring
    • C07C235/58Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton with carbon atoms of carboxamide groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring with carbon atoms of carboxamide groups and singly-bound oxygen atoms, bound in ortho-position to carbon atoms of the same non-condensed six-membered aromatic ring
    • C07C235/60Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton with carbon atoms of carboxamide groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring with carbon atoms of carboxamide groups and singly-bound oxygen atoms, bound in ortho-position to carbon atoms of the same non-condensed six-membered aromatic ring having the nitrogen atoms of the carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C235/00Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
    • C07C235/70Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups and doubly-bound oxygen atoms bound to the same carbon skeleton
    • C07C235/84Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups and doubly-bound oxygen atoms bound to the same carbon skeleton with the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a six-membered aromatic ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F1/00Compounds containing elements of Groups 1 or 11 of the Periodic Table
    • C07F1/04Sodium compounds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Abstract

La presente invención describe métodos mejorados para la síntesis de ácido N-(8-[2-hidroxibenzoil]-amino)caprílico. Ciertos compuestos se han encontrado útiles para prevenir la formación de una impureza coloreada cuando se incluyen en una reacción de hidrólisis de éster. También se ha encontrado que la conducción de hidrólisis de éster en condiciones anaeróbicas minimiza la formación de la impureza de color. También se describen métodos mejorados para sintetizar la sal de sodio de ácido N-(8-[2-hidroxibenzoil]-amino)caprílico.
MX2009002121A 2006-09-07 2007-08-30 Proceso para la manufactura del acido n-(8-[2-hidroxibenzoil]-amin o)caprilico. MX2009002121A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US84277506P 2006-09-07 2006-09-07
PCT/EP2007/059037 WO2008028859A1 (en) 2006-09-07 2007-08-30 A process for the manufacture of snac (salcaprozate sodium)

Publications (1)

Publication Number Publication Date
MX2009002121A true MX2009002121A (es) 2009-05-20

Family

ID=38702068

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2009002121A MX2009002121A (es) 2006-09-07 2007-08-30 Proceso para la manufactura del acido n-(8-[2-hidroxibenzoil]-amin o)caprilico.

Country Status (12)

Country Link
US (3) US10875826B2 (es)
EP (1) EP2064175B1 (es)
JP (1) JP5021033B2 (es)
KR (1) KR101081149B1 (es)
CN (1) CN101506147B (es)
AU (1) AU2007293916B2 (es)
BR (1) BRPI0716539A2 (es)
CA (1) CA2662080C (es)
ES (1) ES2498519T3 (es)
IL (1) IL197014A (es)
MX (1) MX2009002121A (es)
WO (1) WO2008028859A1 (es)

Families Citing this family (39)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8895777B2 (en) * 2006-08-31 2014-11-25 Emisphere Technologies Inc Compounds and compositions for delivering active agents
ES2498519T3 (es) * 2006-09-07 2014-09-24 F. Hoffmann-La Roche Ag Un procedimiento para la fabricación de SNAC (SALCAPROZATO SÓDICO)
JP5902194B2 (ja) 2010-12-16 2016-04-13 ノヴォ ノルディスク アー/エス Glp−1アゴニストとn−(8−(2−ヒドロキシベンゾイル)アミノ)カプリル酸の塩とを含む固形組成物
ES2612278T3 (es) 2011-04-12 2017-05-16 Novo Nordisk A/S Derivados de GLP-1 doble-acilados
ES2952874T3 (es) 2012-03-22 2023-11-06 Novo Nordisk As Composiciones de péptidos GLP-1 y preparación de estas
PT2827845T (pt) 2012-03-22 2019-03-29 Novo Nordisk As Composições compreendendo um agente de entrega e sua preparação
JP6356660B2 (ja) 2012-03-22 2018-07-11 ノヴォ ノルディスク アー/エス 送達剤を含む組成物およびその調製
JP6517690B2 (ja) 2012-06-20 2019-05-22 ノヴォ ノルディスク アー/エス ペプチド及び送達剤を含む錠剤製剤
MY172578A (en) 2013-05-02 2019-12-03 Novo Nordisk As Oral dosing of glp-1 compounds
PT3241878T (pt) * 2014-09-25 2020-09-03 Daikin Ind Ltd Composição compreendendo hfc e hfo
CN105566141B (zh) * 2015-12-17 2018-01-26 蚌埠丰原医药科技发展有限公司 一种门冬氨酸缩合物的制备方法
TWI797133B (zh) 2017-06-09 2023-04-01 丹麥商諾佛 儂迪克股份有限公司 用於經口投予的固體組成物
US20200165313A1 (en) 2017-07-19 2020-05-28 Novo Nordisk A/S Egf(a) analogues, preparation, formulations and uses thereof
JP6898518B2 (ja) 2018-02-02 2021-07-07 ノヴォ ノルディスク アー/エス Glp−1アゴニスト、n−(8−(2−ヒドロキシベンゾイル)アミノ)カプリル酸の塩及び滑沢剤を含む固形組成物
TWI829687B (zh) 2018-05-07 2024-01-21 丹麥商諾佛 儂迪克股份有限公司 包含glp-1促效劑與n-(8-(2-羥基苯甲醯基)胺基)辛酸之鹽的固體組成物
CN108689876B (zh) * 2018-06-28 2020-11-27 苏州东南药业股份有限公司 一种8-(2-羟基苯甲酰胺基)辛酸钠的制备方法
WO2021023855A1 (en) 2019-08-07 2021-02-11 Novo Nordisk A/S Solid compositions comprising an egf(a) derivative and a salt of n-(8-(2-hydroxybenzoyl)amino)caprylic acid
US20220323360A1 (en) 2019-09-06 2022-10-13 Novo Nordisk A/S Method and equipment for fractionation of granules for use in pharmaceutical compositions
CN114728042A (zh) 2019-11-06 2022-07-08 诺和诺德股份有限公司 用于痴呆的glp-1受体激动剂
US20220395559A1 (en) 2019-11-07 2022-12-15 Novo Nordisk A/S Solid compositions comprising a glp-1 agonist, an sglt2 inhibitor and a salt of n-(8-(2-hydroxybenzoyl)amino)caprylic acid
JP2023500031A (ja) 2019-11-07 2023-01-04 ノヴォ ノルディスク アー/エス Pcsk9阻害剤およびn-(8-(2-ヒドロキシベンゾイル)アミノ)カプリル酸の塩を含む固形組成物
IT202000003251A1 (it) 2020-02-18 2021-08-18 Dipharma Francis Srl Preparazione di un analgesico non steroideo
US11478533B2 (en) 2020-04-27 2022-10-25 Novo Nordisk A/S Semaglutide for use in medicine
JP2023524695A (ja) 2020-04-29 2023-06-13 ノヴォ ノルディスク アー/エス Glp-1作動薬およびヒスチジンを含む固形組成物
AU2020450589B2 (en) 2020-05-29 2023-11-09 Sciwind Biosciences Co., Ltd. N-[8-(2-hydroxybenzoyl)amino]potassium octanoate crystal polymorph, and preparation method therefor and use thereof
CN113735734B (zh) * 2020-05-29 2023-12-08 杭州先为达生物科技股份有限公司 N-[8-(2-羟基苯甲酰基)氨基]辛酸钾晶体多晶型物及其制备方法和用途
US20230383037A1 (en) 2020-10-16 2023-11-30 Josho Gakuen Educational Foundation Composition
EP4284774A1 (en) 2021-01-29 2023-12-06 Novo Nordisk A/S Novel synthesis of salcaprozic acid by amide formation
US11667614B2 (en) 2021-04-16 2023-06-06 Navinta III Inc. Process for the preparation of highly pure Salcaprozic Acid and pharmaceutically acceptable salts thereof
EP4323330A1 (en) 2021-04-16 2024-02-21 Navinta III Inc Process for the preparation of highly pure salcaprozic acid and pharmaceutically acceptable salts thereof
KR20230173712A (ko) 2021-04-22 2023-12-27 씨비 바이오파마, 인크. 올리고뉴클레오티드의 경구 전달
WO2022264166A1 (en) 2021-06-14 2022-12-22 Mylan Laboratories Limited Process for the preparation of pure salcaprozate sodium
EP4360645A1 (en) 2021-06-25 2024-05-01 Gan & Lee Pharmaceuticals Co., Ltd. Pharmaceutical composition containing glp-1 compound
WO2023285580A1 (en) 2021-07-15 2023-01-19 Novo Nordisk A/S Tablet comprising a salt of n-(8-(2-hydroxybenzoyl)amino)caprylic acid
AU2022311059A1 (en) 2021-07-16 2024-01-18 Novo Nordisk A/S Sodium n-(8-(2- hydroxybenzoyl)amino)caprylate polymorphic form a
WO2023012263A1 (en) 2021-08-04 2023-02-09 Novo Nordisk A/S Solid oral peptide formulations
CN115160178A (zh) * 2022-07-29 2022-10-11 成都普康唯新生物科技有限公司 一种8-(2-羟基苯甲酰胺基)辛酸钠无水晶型的制备方法
CN115108936A (zh) * 2022-07-29 2022-09-27 成都普康唯新生物科技有限公司 无水体系制备8-(2-羟基苯甲酰胺基)辛酸钠无水晶型的方法
CN117466765B (zh) * 2023-12-27 2024-03-15 成都道合尔医药技术有限公司 8-(2-羟基苯甲酰胺基)辛酸钠及其合成方法

Family Cites Families (36)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3840570A (en) 1970-12-07 1974-10-08 Procter & Gamble Process for preparing sterols from tall oil pitch
DE3623397A1 (de) 1986-07-11 1988-01-14 Boehringer Mannheim Gmbh Neue diphosphonsaeurederivate, verfahren zu deren herstellung und diese verbindungen enthaltende arzneimittel
US5717109A (en) 1994-09-08 1998-02-10 Eli Lilly And Company Excitatory amino acid receptor antagonists
US5650386A (en) 1995-03-31 1997-07-22 Emisphere Technologies, Inc. Compositions for oral delivery of active agents
DE19681560T1 (de) 1995-09-11 1998-08-20 Emisphere Tech Inc Verfahren zur Herstellung von omega-Aminoalkansäure-Derivaten aus Cycloalkanonen
JPH09188661A (ja) * 1996-01-10 1997-07-22 Kao Corp ポリオキシアルキレン脂肪酸アミド硫酸エステル塩の製造方法
US7393645B2 (en) 1996-11-05 2008-07-01 Clinical Micro Sensors, Inc. Compositions for the electronic detection of analytes utilizing monolayers
US7381525B1 (en) 1997-03-07 2008-06-03 Clinical Micro Sensors, Inc. AC/DC voltage apparatus for detection of nucleic acids
US6096273A (en) 1996-11-05 2000-08-01 Clinical Micro Sensors Electrodes linked via conductive oligomers to nucleic acids
WO1999014238A1 (en) 1997-09-18 1999-03-25 Hyundai Pharm. Ind. Co., Ltd. Process for the preparation of calcitonin
AU3357800A (en) 1999-02-05 2000-08-25 Emisphere Technologies, Inc. Method of preparing alkylated salicylamides
EP1175390B1 (en) * 1999-04-05 2005-02-02 Emisphere Technologies, Inc. Disodium salts, monohydrates, and ethanol solvates
US6492408B1 (en) 1999-07-21 2002-12-10 Boehringer Ingelheim Pharmaceuticals, Inc. Small molecules useful in the treatment of inflammatory disease
CA2402719C (en) * 2000-03-21 2012-03-20 Emisphere Technologies, Inc. Method of preparing alkylated salicylamides via a dicarboxylate intermediate
WO2001092206A1 (en) 2000-06-02 2001-12-06 Emisphere Technologies, Inc. Method of preparing salicylamides
US6949577B2 (en) 2000-09-13 2005-09-27 Pfizer, Inc. Pharmaceuticals
GB0107924D0 (en) 2001-03-29 2001-05-23 Angeletti P Ist Richerche Bio Inhibitor of hepatitis C virus NS3 protease
JP4494020B2 (ja) 2002-03-15 2010-06-30 メルク・シャープ・エンド・ドーム・コーポレイション Hivインテグラーゼ阻害剤として有用なn−(置換ベンジル)−8−ヒドロキシ−1,6−ナフチリジン−7−カルボキサミド
US20060173046A1 (en) 2003-07-15 2006-08-03 Bell Ian M Hydroxypyridine cgrp receptor antagonists
US7524813B2 (en) 2003-10-10 2009-04-28 Novo Nordisk Health Care Ag Selectively conjugated peptides and methods of making the same
JP2005298463A (ja) * 2004-04-07 2005-10-27 Matsumoto Yushi Seiyaku Co Ltd 開環重合方法
ES2729825T3 (es) 2004-05-06 2019-11-06 Emisphere Tech Inc Formas poliméricas cristalinas de N-[8-(2-hidroxibenzoil)amino]caprilato monosódico
PE20060653A1 (es) 2004-08-31 2006-09-27 Glaxo Group Ltd Derivados triciclicos condensados como moduladores del receptor 5-ht1
JP5011683B2 (ja) * 2004-09-06 2012-08-29 Dic株式会社 多価ヒドロキシ化合物、エポキシ樹脂、及びそれらの製造法、エポキシ樹脂組成物と硬化物
EP1831157A2 (en) 2004-12-22 2007-09-12 Pfizer Limited Nonnucleoside inhibitors of hiv-1 reverse transcriptase
WO2006103686A1 (en) 2005-03-29 2006-10-05 Hetero Drugs Limited An improved process for the preparation of cefixime
CN101258132B (zh) 2005-12-14 2012-04-25 江苏恒瑞医药股份有限公司 用作金属蛋白酶抑制剂的(2,5-二酮咪唑啉-1-基)-n-羟基-乙酰胺
US8198448B2 (en) 2006-07-14 2012-06-12 Amgen Inc. Fused heterocyclic derivatives and methods of use
PE20080403A1 (es) 2006-07-14 2008-04-25 Amgen Inc Derivados heterociclicos fusionados y metodos de uso
US8217177B2 (en) 2006-07-14 2012-07-10 Amgen Inc. Fused heterocyclic derivatives and methods of use
ES2498519T3 (es) * 2006-09-07 2014-09-24 F. Hoffmann-La Roche Ag Un procedimiento para la fabricación de SNAC (SALCAPROZATO SÓDICO)
FR2912145B1 (fr) 2007-02-02 2009-03-06 Servier Lab Nouveaux derives tricycliques,leur procede de preparation et les compositions pharmaceutiques qui les contiennent
AR065804A1 (es) 2007-03-23 2009-07-01 Smithkline Beecham Corp Compuesto de indol carboxamida, composicion farmaceutica que lo comprende y uso de dicho compuesto para preparar un medicamento
US8258312B2 (en) 2007-06-27 2012-09-04 Mylan Laboratories Ltd Process for preparing pure valsartan
WO2009017154A1 (ja) 2007-07-31 2009-02-05 Otsuka Chemical Co., Ltd. ペプチドの製造方法
CN101367750B (zh) 2007-08-14 2012-05-23 中国人民解放军军事医学科学院毒物药物研究所 (1s,2s,3s,4r)-3-[(1s)-1-乙酰氨-2-乙基-丁基]-4-胍基-2-羟基-环戊基-1-羧酸水合物及其医药用途

Also Published As

Publication number Publication date
IL197014A0 (en) 2009-11-18
US10875826B2 (en) 2020-12-29
CN101506147A (zh) 2009-08-12
US20210070691A1 (en) 2021-03-11
WO2008028859A1 (en) 2008-03-13
AU2007293916B2 (en) 2011-02-03
JP5021033B2 (ja) 2012-09-05
CN101506147B (zh) 2012-03-21
US7544833B2 (en) 2009-06-09
EP2064175A1 (en) 2009-06-03
AU2007293916A1 (en) 2008-03-13
US20200071263A1 (en) 2020-03-05
BRPI0716539A2 (pt) 2016-11-01
ES2498519T3 (es) 2014-09-24
IL197014A (en) 2013-01-31
KR20090060997A (ko) 2009-06-15
JP2010502667A (ja) 2010-01-28
CA2662080A1 (en) 2008-03-13
KR101081149B1 (ko) 2011-11-07
US20080064890A1 (en) 2008-03-13
EP2064175B1 (en) 2014-08-06
CA2662080C (en) 2012-07-17

Similar Documents

Publication Publication Date Title
MX2009002121A (es) Proceso para la manufactura del acido n-(8-[2-hidroxibenzoil]-amin o)caprilico.
NZ600119A (en) Process and intermediates for the preparation of 5-biphenyl-4-yl-2-methylpentanoic acid derivatives
NZ611898A (en) Compounds for inhibiting mitotic progression
IL196894A0 (en) Process for preparing 3-dihalomethylpyrazole-4-carboxylic acid derivatives
TW200616646A (en) Synthesis of boronic ester and acid compounds
TN2009000077A1 (en) Process for preparing biaryl substituted 4-amino-butyric acid or derivatives thereof and their use in the production of nep inhibitors
UA102817C2 (ru) Способ синтеза агомелатина
WO2008062460A3 (en) Crystalline forms of pregabalin
UA102220C2 (ru) Способ синтеза агомелатина
MX2012003914A (es) Metodo para la fabricacion de acidos aminohidroxi difosfonicos.
WO2007039522A3 (en) Process for esterification of an organic acid
WO2011077140A3 (en) Method of producing acrylic and methacrylic acid
MY143324A (en) Process for preparing phosphorus compounds having phosphate-phosphonate bond
GEP20115344B (en) New process for synthesis of agomelatine
AR071259A1 (es) Procedimiento para preparar un acido gamma-amino sustituido y composiciones farmaceuticas que contienen dicho compuesto
WO2009044409A3 (en) Novel resolution process for pregabalin
HK1114848A1 (en) Process for preparation of high-purity meloxicam and meloxicam potassium salt
HK1123275A1 (en) Novel method for preparing quaternary acid and ammonium salts
ZA200810024B (en) Process for the synthesis of ibandronate sodium
MX2011012588A (es) Metodo para la fabricacion de acidos aminopolialquilenfosfonicos.
UA102091C2 (ru) Способ получения сульфонилпиролов как ингибиторов hdac
MXPA05012113A (es) Procedimiento para sintetizar intermediarios inhibidores de beta-lactamasa.
MX2009001508A (es) Un proceso novedoso para preparar ester de acido 3-amino-5-fluoro-4-dialcoxipentanoico.
FR2914641B1 (fr) Procede de co-production de carbonates non cycliques et d'amino-acides
MXPA05013944A (es) Nuevo procedimiento para la produccion de melagatran.

Legal Events

Date Code Title Description
FG Grant or registration