NO20063917L - Fremgangsmate for syntese av N-[3-(3-cyanopyrazol[1,5A]pyrimidin-7-yl)-fenyl]-N-etyl-acetamid - Google Patents

Fremgangsmate for syntese av N-[3-(3-cyanopyrazol[1,5A]pyrimidin-7-yl)-fenyl]-N-etyl-acetamid

Info

Publication number
NO20063917L
NO20063917L NO20063917A NO20063917A NO20063917L NO 20063917 L NO20063917 L NO 20063917L NO 20063917 A NO20063917 A NO 20063917A NO 20063917 A NO20063917 A NO 20063917A NO 20063917 L NO20063917 L NO 20063917L
Authority
NO
Norway
Prior art keywords
formula
phenyl
ethyl
acetamide
synthesis
Prior art date
Application number
NO20063917A
Other languages
English (en)
Inventor
Katalin Szoke
Laszlo Czibula
Laszlo Dobay
Eva Werkne Papp
Judit Nagyne Bagdy
Gabor Tarkanyi
Original Assignee
Richter Gedeon Vegyeszet
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 Richter Gedeon Vegyeszet filed Critical Richter Gedeon Vegyeszet
Publication of NO20063917L publication Critical patent/NO20063917L/no

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P21/00—Drugs for disorders of the muscular or neuromuscular system
    • A61P21/02—Muscle relaxants, e.g. for tetanus or cramps
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/08—Antiepileptics; Anticonvulsants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/20—Hypnotics; Sedatives
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/22—Anxiolytics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00—Carboxylic acid amides
    • C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C233/34—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups
    • C07C233/42—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring
    • C07C233/43—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring having the carbon atom of the carboxamide group bound to a hydrogen atom or to a carbon atom of a saturated carbon skeleton

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Engineering & Computer Science (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Pain & Pain Management (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Anesthesiology (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

Oppfinnelsen angår N-[3-(3-cyanopyrazol[1,5-a]-pyrimidin-7-yl)-fenyl]-N-etyl-acetamid som har formel (IV), inneholdende mindre enn 0,2% urenheter, som er egnet for terapeutisk anvendelse. Videre angår oppfinnelsen en fremgangsmåte for syntetiseringen av terapeutisk anvendelige forbindelser som har formel (IV), inneholdende mindre enn 0,2% urenheter, ved å omsette det nye mellomproduktet N-{3-[3-(dimetylamino)-1-okso-2-propenyl]-fenyl}-N-etyl-acetamidhydroklorid som har formel (II), med 3-amino-4-pyrazol-karbonitrilbase som har formel (III), i et syrefritt medium. Oppfinnelsen angår også det nye N-{3-[3-(dimetylamino)-l-okso-2propenyll-fenyl}-N-etyl-acetamid-hydroklorid som har formel (II). Oppfinnelsen angår også en fremgangsmåte for syntetiseringen av det nye N-{3-[3-(dimetylamino)-l-okso-2propenyl]-fenyl}-N-etyl-acetamid-hydroklorid som har formel (II), som har en renhet på mer enn 99,5%. Videre angår oppfinnelsen N-{3-[3-cyanopyrazol(1,5-a)-pyrimidin]-6-y1-3-[(3-N-etylacetamidofenyl)-3-oksopropen-1-yl]-(pyrimidin-7-yl)-fenyl}-N-etyl-acetamid som har formel (V), som er en isolert ny urenhet dannet i 0,07% utbytte under syntetiseringen av forbindelsen som har formel (IV).
NO20063917A 2004-02-02 2006-09-01 Fremgangsmate for syntese av N-[3-(3-cyanopyrazol[1,5A]pyrimidin-7-yl)-fenyl]-N-etyl-acetamid NO20063917L (no)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
HU0400325A HUP0400325A3 (en) 2004-02-02 2004-02-02 Pure n-[3-(-cyanopyrazolo[1,5-a]pyrimidin-7-yl)phenyl]-n-ethyl-acetamide, process for its preparation and intermediates
PCT/HU2005/000008 WO2005073235A2 (en) 2004-02-02 2005-01-31 Process for the synthesis of n- [3-(3-cyanopyrazolo [1,5a] pyrimidin-7-yl)-phenyl]-n-ethyl-acetamide

Publications (1)

Publication Number Publication Date
NO20063917L true NO20063917L (no) 2006-11-01

Family

ID=89981959

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20063917A NO20063917L (no) 2004-02-02 2006-09-01 Fremgangsmate for syntese av N-[3-(3-cyanopyrazol[1,5A]pyrimidin-7-yl)-fenyl]-N-etyl-acetamid

Country Status (9)

Country Link
EP (2) EP1711501B1 (no)
JP (1) JP2007519700A (no)
AT (2) ATE438647T1 (no)
DE (2) DE602005015902D1 (no)
EA (1) EA010830B1 (no)
HU (1) HUP0400325A3 (no)
NO (1) NO20063917L (no)
RS (1) RS20060427A (no)
WO (1) WO2005073235A2 (no)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005099712A2 (en) * 2004-04-19 2005-10-27 Sanmar Speciality Chemicals Limited Process for preparation of n-[3-(3-cyanopyrazolo [1,5-a]pyrimidin-7-yl)phenyl]-n-ethylacetamide
WO2006070244A2 (en) * 2004-11-22 2006-07-06 Bakulesh Mafatlal Khamar A process for the preparation of zaleplon

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4626538A (en) 1983-06-23 1986-12-02 American Cyanamid Company [7-(3-disubstituted amino)phenyl]pyrazolo[1,5-a]pyrimidines
US5714607A (en) * 1995-12-01 1998-02-03 American Cyanamid Company Process improvement in the synthesis of N- 3-(3-cyano-pyrazolo 1,5-a!pyrimidin-7-yl)phenyl!-N-ethylacetamide
ES2223311T1 (es) * 2001-06-12 2005-03-01 Biogal Gyogyszergyar Rt. Procedimiento para la preparacion de n-(3-(3-cianopirazol(1,5-a)pirimidin-7-il)fenil)-n-etilacetamida (zaleplon).
PL374176A1 (en) * 2001-08-01 2005-10-03 Biogal Gyogyszergyar Rt Process for purifying n-[3-(3-cyanopyrazolo[1,5-a]pyrimidin-7-yl)phenyl]-n-ethylacetamide(zaleplon) and crystalline forms of zaleplon accessible with the process
PL207322B1 (pl) * 2002-05-14 2010-11-30 Adamed Społka Z Ograniczoną Odpowiedzialnością Sposób wytwarzania zaleplonu

Also Published As

Publication number Publication date
EP1950213B1 (en) 2009-08-05
WO2005073235A3 (en) 2005-10-06
RS20060427A (sr) 2008-08-07
HU0400325D0 (en) 2004-04-28
DE602005015902D1 (de) 2009-09-17
HUP0400325A2 (hu) 2005-09-28
DE602005012365D1 (de) 2009-03-05
HUP0400325A3 (en) 2005-11-28
EA200601417A1 (ru) 2006-12-29
EP1711501B1 (en) 2009-01-14
JP2007519700A (ja) 2007-07-19
ATE438647T1 (de) 2009-08-15
ATE420882T1 (de) 2009-01-15
EA010830B1 (ru) 2008-12-30
EP1711501A2 (en) 2006-10-18
EP1950213A3 (en) 2008-08-13
WO2005073235A2 (en) 2005-08-11
EP1950213A2 (en) 2008-07-30

Similar Documents

Publication Publication Date Title
AU2009260044B2 (en) A process for the preparation of the apoptosis promoter ABT-263
EP1682503B1 (fr) Derives de n-[phenyl(alkylpiperidin-2-yl)methyl]benzamide, leur preparation et leur application en therapeutique
US5756817A (en) O-carbamoyl-phenylalaninol compounds, their pharmaceutically useful salts and process for preparing the same
JP4319245B2 (ja) ヒスタミン−3受容体拮抗薬
EP1527048B1 (fr) Derives de n-[phenyl(piperidin-2-yl)methyl]benzamide, leur preparation et leur application en therapeutique
ES2199433T3 (es) 3,3-diarilpropilaminas, su uso y su preparacion.
AU2004247487B2 (en) N-pyrrolidin-3-YL-amide derivatives as serotonin and noradrenaline re-uptake inhibitors
US20130158265A1 (en) Sitagliptin, salts and polymorphs thereof
OA11572A (en) PyrroloÄ2,3-düpyrimidine compounds.
WO1998015526A1 (en) O-carbamoyl-phenylalaninol compounds, their pharmaceutically useful salts and process for preparing the same
JPS58172379A (ja) 新規なキナゾリン誘導体
ES2259475T3 (es) Sintesis de compuestos utiles en la fabricacion de ketorolac.
CA2189964A1 (en) Novel diaminomethylidene derivative
KR102611847B1 (ko) 무스카린 수용체 길항 활성을 갖는 신규한 피롤리디늄 화합물 및 이의 용도
WO2005073235A3 (en) Process for the synthesis of n- [3-(3-cyanopyrazolo [1,5a] pyrimidin-7-yl)-phenyl]-n-ethyl-acetamide
CN113121417A (zh) 一种新型哌啶衍生物及其药物用途
JPH1072426A (ja) 新規ムスカリン様レセプターアゴニスト
JP6368043B2 (ja) 三環式ラクタム化合物の製造法
WO2009084031A2 (en) An improved process for preparation of (2e)-2-cyano-3-(3,4- dihydroxy-5-nitrophenyl)n,n-diethyl-2-propenamide polymorphic form a
KR100998067B1 (ko) 비스(1-[(4-클로로페닐)페닐메틸]피페라진)-2,3-디벤조일 타르타르산 신규 중간체 염 및 이를 이용한 광학 활성적으로 순수한 1-[(4-클로로페닐)페닐메틸]피페라진을 분리하는 분리방법
EP1716129A1 (en) Piperazine derivatives which exhibit acivity as serotonin and noradrenaline re-upatke inhibitors
CA3232921A1 (en) Oximes and their use in treatment of gba-related diseases
EP2396334A1 (fr) Derives de n-[(2-aza-bicyclo[2.1.1]hex-1-yl]-aryl-methyl]-benzamide, leur preparation et leur application en therapeutique
HK1154568B (en) A process for the preparation of the apoptosis promoter abt-263
NO843307L (no) Cykloheksankarbonksylsyrer og derivater derav

Legal Events

Date Code Title Description
FC2A Withdrawal, rejection or dismissal of laid open patent application