[go: up one dir, main page]

PE20071150A1 - Un proceso para preparar derivados de tetrahidroquinolina - Google Patents

Un proceso para preparar derivados de tetrahidroquinolina

Info

Publication number
PE20071150A1
PE20071150A1 PE2007000358A PE2007000358A PE20071150A1 PE 20071150 A1 PE20071150 A1 PE 20071150A1 PE 2007000358 A PE2007000358 A PE 2007000358A PE 2007000358 A PE2007000358 A PE 2007000358A PE 20071150 A1 PE20071150 A1 PE 20071150A1
Authority
PE
Peru
Prior art keywords
trifluoromethyl
ethyl
ona
quinolin
dihydro
Prior art date
Application number
PE2007000358A
Other languages
English (en)
Inventor
Masaki Okamoto
Akira Sakuragi
Yoshikazu Mori
Takeshi Hamada
Hitoshi Kubota
Yoshinori Nakamura
Takanori Higashijima
Norimitsu Hayashi
Original Assignee
Mitsubishi Tanabe Pharma Corp
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 Mitsubishi Tanabe Pharma Corp filed Critical Mitsubishi Tanabe Pharma Corp
Publication of PE20071150A1 publication Critical patent/PE20071150A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom 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
    • C07D215/38Nitrogen atoms
    • C07D215/42Nitrogen atoms attached in position 4
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/06Antihyperlipidemics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom 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
    • C07D215/20Oxygen atoms
    • C07D215/22Oxygen atoms attached in position 2 or 4
    • C07D215/233Oxygen atoms attached in position 2 or 4 only one oxygen atom which is attached in position 4

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Hematology (AREA)
  • Diabetes (AREA)
  • Obesity (AREA)
  • Urology & Nephrology (AREA)
  • Vascular Medicine (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Quinoline Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

SE REFIERE A UN PROCEDIMIENTO DE PREPARACION DE UN COMPUESTO DE FORMULA (I-a) O (2R,4S)-2-ETIL-6-TRIFLUOROMETIL-1,2,3,4-TETRAHIDROQUINOLIN-4-ILAMINA, QUE COMPRENDE: A) HACER REACCIONAR ACIDO (R)-3-AMINOVALERICO O SU ESTER ALQUILICO CON UN COMPUESTO DE FORMULA (I-f) PARA FORMAR ACIDO (R)-3-(4-TRIFLUOROMETIL-FENILAMINO)-VALERICO, DONDE L ES UN GRUPO SALIENTE; B) HACER REACCIONAR ACIDO (R)-3-(4-TRIFLUOROMETIL-FENILAMINO)-VALERICO CON PENTOXIDO DE FOSFORO EN PRESENCIA DE ACIDO METANSULFONICO PARA FORMAR (R)-2-ETIL-6-TRIFLUOROMETIL-2,3-DIHIDRO-1H-QUINOLIN-4-ONA; C) CONVERTIR (R)-2-ETIL-6-TRIFLUOROMETIL-2,3-DIHIDRO-1H-QUINOLIN-4-ONA EN OXIMA DE (R)-2-ETIL-6-TRIFLUOROMETIL-2,3-DIHIDRO-1H-QUINOLIN-4-ONA O EN O-ALQUIALQUIL-OXIMA DE (R)-2-ETIL-6-TRIFLUOROMETIL-2,3-DIHIDRO-1H-QUINOLIN-4-ONA; Y D) REALIZAR UNA REDUCCION CATALITICA DE LA OXIMA U O-ALQUIALQUIL-OXIMA EN PRESENCIA DEL CATALIZADOR DE PALADIO-CARBONO. SE REFIERE TAMBIEN A UN PROCEDIMIENTO DE PREPARACION DE COMPUESTOS DE FORMULA (I), (II), ENTRE OTROS. DICHO COMPUESTO OBTENIDO ES INHIBIDOR DE LA PROTEINA DE TRANSFERENCIA DE ESTER DE COLESTERILO (CETP) SIENDO UTIL EN EL TRATAMIENTO DE HIPERLIPIDEMIA
PE2007000358A 2006-03-30 2007-03-29 Un proceso para preparar derivados de tetrahidroquinolina PE20071150A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2006092783 2006-03-30
JP2006322845 2006-11-30

Publications (1)

Publication Number Publication Date
PE20071150A1 true PE20071150A1 (es) 2007-12-03

Family

ID=38123770

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2007000358A PE20071150A1 (es) 2006-03-30 2007-03-29 Un proceso para preparar derivados de tetrahidroquinolina

Country Status (10)

Country Link
US (1) US8084611B2 (es)
EP (2) EP2007728B1 (es)
JP (1) JP5275971B2 (es)
AR (1) AR060174A1 (es)
AT (1) ATE533747T1 (es)
ES (1) ES2374315T3 (es)
PE (1) PE20071150A1 (es)
TW (1) TW200808731A (es)
UY (1) UY30244A1 (es)
WO (1) WO2007116922A1 (es)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AR069165A1 (es) 2007-11-05 2010-01-06 Novartis Ag Derivados de 4-bencilamino-1-carboxacilpiperidina como inhibidores de cetp utiles para el tratamiento de hiperlipidemia
WO2009071509A1 (en) * 2007-12-03 2009-06-11 Novartis Ag 1,2-disubstituted-4-benzylamino-pyrrolidine derivatives as cetp inhibitors useful for the treatment of diseases such as hyperli pidemia or arteriosclerosis
CN102020608B (zh) * 2010-09-17 2012-09-05 清华大学 喹啉化合物的制备方法
SG11201701077XA (en) 2014-08-12 2017-03-30 Dezima Pharma B V Process for preparing synthetic intermediates for preparing tetrahydroquinoline derivatives
WO2017023165A1 (en) * 2015-08-04 2017-02-09 Dezima Pharma B.V. Pharmaceutical composition and therapeutic combination comprising a cholesteryl ester transfer protein inhibitor and an atp citrate lyase inhibitor – ampk activator
US10085999B1 (en) 2017-05-10 2018-10-02 Arixa Pharmaceuticals, Inc. Beta-lactamase inhibitors and uses thereof
CA3077474A1 (en) 2017-10-02 2019-04-11 Arixa Pharmaceuticals, Inc. Aztreonam derivatives and uses thereof
EP3590927A1 (en) 2018-07-05 2020-01-08 Bayer Animal Health GmbH Novel compounds for controlling arthropods
JP7437847B2 (ja) 2018-10-01 2024-02-26 アリクサ ファーマシューティカルズ、インコーポレイテッド レレバクタムの誘導体およびその使用
JP2022524118A (ja) 2019-03-12 2022-04-27 アリクサ ファーマシューティカルズ、インコーポレイテッド アビバクタム誘導体の結晶形
WO2020219258A1 (en) 2019-04-25 2020-10-29 Arixa Pharmaceuticals, Inc. Methods of synthesizing aztreonam derivatives
TWI843678B (zh) * 2019-06-18 2024-05-21 美商美國禮來大藥廠 用於製備2-(2,6-二氯苯基)-1-[(1s,3r)-3-(羥甲基)-5-(3-羥基-3-甲基丁基)-1-甲基-3,4-二氫異喹啉-2(1h)-基]乙烯酮之方法及中間物
MX2023006056A (es) 2020-11-25 2023-06-06 Akagera Medicines Inc Nanoparticulas lipidicas para suministro de acidos nucleicos y metodos de uso de las mismas.
LT4125911T (lt) 2021-03-05 2024-08-12 Newamsterdam Pharma B.V. Obicetrapibas demencijų gydymui
US20230041138A1 (en) 2021-07-26 2023-02-09 NewAmsterdam Pharma B.V. (Dutch Registration No. 55971946) Treatment of his hyporesponders
EP4456872A1 (en) 2021-12-30 2024-11-06 NewAmsterdam Pharma B.V. Obicetrapib and sglt2 inhibitor combination
CN114516865B (zh) * 2022-03-09 2023-06-23 成都师范学院 一类D-π-A型有机共轭分子及其制备方法和应用
KR20250031230A (ko) 2022-05-25 2025-03-06 아카제라 메디신즈, 인크. 핵산 전달을 위한 지질 나노입자 및 이의 사용 방법
AU2023303916A1 (en) 2022-07-05 2025-01-30 Newamsterdam Pharma B.V. Salts of obicetrapib and processes for their manufacture and intermediates thereof
TW202416994A (zh) 2022-08-22 2024-05-01 荷蘭商新阿姆斯特丹製藥公司 固定劑量醫藥組合物及其用途
EP4661865A1 (en) 2023-02-07 2025-12-17 NewAmsterdam Pharma B.V. Obicetrapib and ezetimibe combination treatment and fixed dose pharmaceutical compositions
WO2025059594A1 (en) 2023-09-15 2025-03-20 Newamsterdam Pharma B.V. METHODS FOR TREATING HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA (HeFH)
WO2025093436A1 (en) 2023-11-01 2025-05-08 Newamsterdam Pharma B.V. Treatment and prevention of age-related macular degeneration using a cetp inhibitor
WO2025093129A1 (en) 2023-11-01 2025-05-08 Newamsterdam Pharma B.V. Treatment and prevention of age-related macular degeneration using a cetp inhibitor
WO2025146262A1 (en) 2024-01-03 2025-07-10 Newamsterdam Pharma B.V. Obicetrapib for use in the treatment of hemoglobinopathies
WO2025146415A1 (en) 2024-01-03 2025-07-10 Newamsterdam Pharma B.V. Improvement in atherosclerotic plaque characteristics with obicetrapib

Family Cites Families (36)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FI82094C (fi) 1989-02-16 1997-09-09 Valmet Corp Anvaendning av en legering av ett metallpulver och en karbid eller nitrid innefattande belaeggningskomposition foer en i en pappersmaskin anvaendbar yankeecylinder
DE69029668T2 (de) 1989-03-08 1997-08-07 Merck Sharp & Dohme Tetrahydroquinolin-Derivate, verwendbar bei neurodegenerativen Krankheiten
ATE117294T1 (de) 1989-08-11 1995-02-15 Ici Plc Chinolin-derivate, verfahren zu ihrer herstellung und ihre anwendung als arzneimittel.
JPH03161360A (ja) 1989-11-21 1991-07-11 Tdk Corp サーマルヘッド
JPH03216566A (ja) 1990-01-22 1991-09-24 Mitsubishi Electric Corp Ccdリニアイメージセンサのテスト装置
GB9010394D0 (en) 1990-05-09 1990-06-27 Ici Plc Heterocyclic compounds
IE914573A1 (en) 1991-01-17 1992-07-29 Ici Plc Boron compounds
JPH05213884A (ja) 1991-06-14 1993-08-24 Upjohn Co:The 新規な4−アミノキノリン類およびこれを有効成分とする高血圧・鬱血性心不全の予防・治療剤
US5576460A (en) 1994-07-27 1996-11-19 Massachusetts Institute Of Technology Preparation of arylamines
US5929281A (en) 1996-04-19 1999-07-27 Tosoh Corporation Process for producing heterocyclic aromatic amine or arylamine
GT199900147A (es) * 1998-09-17 1999-09-06 1, 2, 3, 4- tetrahidroquinolinas 2-sustituidas 4-amino sustituidas.
US6197786B1 (en) 1998-09-17 2001-03-06 Pfizer Inc 4-Carboxyamino-2-substituted-1,2,3,4-tetrahydroquinolines
US6147090A (en) * 1998-09-17 2000-11-14 Pfizer Inc. 4-carboxyamino-2-methyl-1,2,3,4,-tetrahydroquinolines
HN2000000203A (es) 1999-11-30 2001-06-13 Pfizer Prod Inc Procedimiento para la obtencion de 1,2,3,4-tetrahidroquinolinas 4-carboxiamino-2- sustituidas.
EP1167521A1 (en) 2000-06-30 2002-01-02 Aventis Animal Nutrition S.A. Coated enzyme-containing catalyst
WO2002008869A2 (en) 2000-07-25 2002-01-31 Digeo, Inc. Allowance account for interactive television system
JP2002053557A (ja) * 2000-08-14 2002-02-19 Japan Tobacco Inc アポリポ蛋白a−i産生促進薬
EP1288205B1 (en) * 2000-08-18 2011-02-02 Ajinomoto Co., Inc. Novel phenylalanine derivatives
SE0101161D0 (sv) * 2001-03-30 2001-03-30 Astrazeneca Ab New compounds
DE60210265T2 (de) 2001-04-30 2006-10-12 Pfizer Products Inc., Groton Verfahren und zwischenprodukte zur herstellung von 4-aminochinolin-cetp-inhibitoren
EP1318139A3 (en) 2001-12-07 2003-07-30 Solvias AG Processes for the preparation of 3-aminocarboxylic acids and their esters
US6903233B2 (en) 2002-03-11 2005-06-07 Takasago International Corporation Process for producing optically active 3-halogenocarboxylic acid ester and 3-azidocarboxylic acid ester
EP1829858A3 (en) 2002-08-30 2007-10-03 Japan Tobacco, Inc. Dibenzylamine compounds and pharmaceutical use thereof
KR20050055747A (ko) 2002-10-04 2005-06-13 밀레니엄 파머슈티컬스 인코퍼레이티드 염증 질환 치료용의 pgd2 수용체 길항제
JP2004238322A (ja) 2003-02-05 2004-08-26 Sumika Fine Chemicals Co Ltd (r)−3−アミノペンタンニトリルメタンスルホン酸塩の製造方法
WO2004072041A1 (en) 2003-02-12 2004-08-26 Care X S.A. Tetrahydroquinolines as agonists of liver- x receptors
EP1594843B1 (en) 2003-02-18 2013-05-22 Takasago International Corporation METHOD FOR PRODUCING AN OPTICALLY ACTIVE beta-amino acid derivative
CN1795177A (zh) 2003-03-28 2006-06-28 辉瑞产品公司 作为治疗动脉粥样硬化和肥胖症的cetp抑制剂的 1 , 2 , 4 , -取代的1,2,3,4,-四氢-和1,2二氢-喹啉以及1, 2 , 3 , 4-四氢-喹喔啉衍生物
JP2004339205A (ja) 2003-04-24 2004-12-02 Ajinomoto Co Inc 光学活性N−アリール−β−アミノ酸化合物の製造方法
US7145030B2 (en) 2003-04-24 2006-12-05 Ajinomoto Co., Inc. Production method for optically active N-aryl-β-amino acid compounds
ATE455088T1 (de) 2003-09-18 2010-01-15 Takasago Perfumery Co Ltd Asymmetrische reduktive aminierung von ketosäurederivaten zur herstellung von aminosäurederivaten
JP2007528403A (ja) * 2004-03-09 2007-10-11 エラン ファーマシューティカルズ,インコーポレイテッド 二環式アスパラギン酸プロテアーゼ阻害薬を用いるアミロイドーシスの処置方法
ATE402180T1 (de) 2004-03-26 2008-08-15 Lilly Co Eli Verbindungen zur behandlung von dyslipidemie
UA90269C2 (ru) 2004-04-02 2010-04-26 Мицубиси Танабе Фарма Корпорейшн Тетрагидрохинолиновые производные и способ их получения
JP2005336083A (ja) 2004-05-26 2005-12-08 Sumitomo Chemical Co Ltd 芳香族アミノ化合物の製造方法
KR20070041452A (ko) 2004-06-24 2007-04-18 일라이 릴리 앤드 캄파니 이상지혈증 치료를 위한 화합물 및 방법

Also Published As

Publication number Publication date
TW200808731A (en) 2008-02-16
US8084611B2 (en) 2011-12-27
EP2154132A1 (en) 2010-02-17
JP5275971B2 (ja) 2013-08-28
ES2374315T3 (es) 2012-02-15
WO2007116922A1 (en) 2007-10-18
AR060174A1 (es) 2008-05-28
JP2009532345A (ja) 2009-09-10
US20090292125A1 (en) 2009-11-26
EP2007728A1 (en) 2008-12-31
ATE533747T1 (de) 2011-12-15
EP2007728B1 (en) 2011-11-16
UY30244A1 (es) 2007-11-30

Similar Documents

Publication Publication Date Title
PE20071150A1 (es) Un proceso para preparar derivados de tetrahidroquinolina
PE20020340A1 (es) Composicion farmaceutica que comprende ester etilico de acido [2r,4s]-4-[(3,5-bis-trifluorometilbencil)metoxicarbonilamino]-2-etil-6-trifluorometil-3,4-dihidro-2h-quinolina-1-carboxilico y atorvastatina o sus metabolitos hidroxilicos
MA31834B1 (fr) 5-[(3,3,3-trifluoro-2-hydroxy-1-arylpropyl)amino]-1h-quinolin-2-ones, leur procédé de production et leur utilisation comme anti-inflammatoires
MA34767B1 (fr) Compositions et procédés pour la modulation de fxr
PE44599A1 (es) Inhibidores de la enzima acido nitrico sintasa
BRPI0712631B8 (pt) compostos, processos para a preparação de um composto, composição farmacêutica, uso de um composto e combinações
CU20090206A7 (es) Solución novedosa no-acuosa tópica de diclofenaco y proceso para su preparación
MA30652B1 (fr) Composes organiques
MXPA05006907A (es) Compuestos diazoicos cationicos, composiciones que los contienen como colorante directo, procedimiento de coloracion de fibras queratinicas y dispositivo.
MA37891B1 (fr) Alcoxypyrazoles comme activateurs de guanylate cyclase soluble
WO2008062478A3 (en) Improved process for pure montelukast sodium through pure intermediates as well as novel amine salts
MX2009003823A (es) Nueva difenilazetidinona sustituida con acido piperazina-1-sulfonico y que tiene propiedades farmacologicas mejoradas.
CO5261552A1 (es) Procedimiento para la obtencion de 1,2,3,4-tetrahidroquino- linas 4-carboxiamino-2-sustituidas
BRPI0408353A (pt) composto, composição farmacêutica, métodos para o tratamento de neoplasias suscetìveis e para o tratamento de infecções virais, e, uso de um composto
EA200900090A1 (ru) Бензиламины, способ их получения и их применение в качестве противовоспалительных средств
GR3021014T3 (en) 2-Substituted quinolines, process for their preparation as well as their use in medicaments
BR112015011974A2 (pt) derivados de azaquinazolina carboxamida
ATE380816T1 (de) Substituierte imidazopyrimidine zur prävention und behandlung von krebs
EA199900948A1 (ru) Способ получения 2-арил-3-арил-5-галогенпиридинов, используемых в качестве ингибиторов cox-2
HN2000000045A (es) Nuevas combinaciones farmaceuticas para inhibidores de la nos.
BRPI0411308A (pt) composto, composição farmacêutica, processo para a preparação de um composto, e, uso de um composto
AR008993A1 (es) Sales de esteres etilicos de acidos 3-(2-(4-(4-(amino-imino-metil)-fenil)-4 -metil-2,5-dioxo-imidazolidin-1-il)-acetilamino)-3-fenil-propionicos
MX2009005249A (es) Compuestos organicos.
MA33917B1 (fr) Dérivés d'acide carboxylique ayant un cycle oxazolopyrimidine 2,5-substitue
BR112012017447A2 (pt) derivados de ácidos carboxílicos heterocíclicos tendo um anel oxazolopirimidina 2,5-substituído

Legal Events

Date Code Title Description
FC Refusal