AR058572A1 - 3-(4-piperidinil)-2,3,4,5-tetrahidro-1,3-benzodiazepin-2(1h)-ona - Google Patents

3-(4-piperidinil)-2,3,4,5-tetrahidro-1,3-benzodiazepin-2(1h)-ona

Info

Publication number
AR058572A1
AR058572A1 ARP060105634A ARP060105634A AR058572A1 AR 058572 A1 AR058572 A1 AR 058572A1 AR P060105634 A ARP060105634 A AR P060105634A AR P060105634 A ARP060105634 A AR P060105634A AR 058572 A1 AR058572 A1 AR 058572A1
Authority
AR
Argentina
Prior art keywords
formula
group
phenylmethyl
piperidinyl
nitro
Prior art date
Application number
ARP060105634A
Other languages
English (en)
Original Assignee
Boehringer Ingelheim Int
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 Boehringer Ingelheim Int filed Critical Boehringer Ingelheim Int
Publication of AR058572A1 publication Critical patent/AR058572A1/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D243/00—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms
    • C07D243/04—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 3
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • 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
    • A61P25/06—Antimigraine agents
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Engineering & Computer Science (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pain & Pain Management (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

Reivindicacion 1: Procedimiento para preparar el compuesto de la formula (1) caracterizado porque (a) se hace reaccionar ácido 2-nitrofenilacético con 4-amino-N-fenilmetilpiperidina en 2-nitro-N-[1-fenilmetil)-4-piperidinil]-fenilacetamida de la formula (2); (b) se hidrogena el grupo nitro de la 2-nitro-N-[1-(fenilmetil)-4-piperidinil]-fenilacetamida obtenida de la formula 2 en el grupo amino, con lo cual se produce el compuesto de la formula (3); (c) se hace reaccionar el producto intermediario de la formula 3 por adicion de un éster y en presencia de una base en un carbamato de la formula general (4) en donde R1 es un grupo fenilo, bencilo, alilo, 2,2,2-tricloroetilo o un grupo alquilo C1-6 lineal o ramificado, y (d) se disuelve el compuesto obtenido de la formula general 4 en un disolvente orgánico aprotico, se convierte el grupo carbonilo por adicion de un agente de reduccion en un grupo metileno y se cicla en 3-[1-(fenilmetil)-4-piperidinil]-2,3,4,5-tetrahidro- 1,3-benzodiazepin-2(1H)-ona de la formula (5).
ARP060105634A 2005-12-24 2006-12-20 3-(4-piperidinil)-2,3,4,5-tetrahidro-1,3-benzodiazepin-2(1h)-ona AR058572A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP05028476 2005-12-24

Publications (1)

Publication Number Publication Date
AR058572A1 true AR058572A1 (es) 2008-02-13

Family

ID=36340767

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP060105634A AR058572A1 (es) 2005-12-24 2006-12-20 3-(4-piperidinil)-2,3,4,5-tetrahidro-1,3-benzodiazepin-2(1h)-ona

Country Status (15)

Country Link
US (1) US7473778B2 (es)
EP (1) EP1968952B1 (es)
JP (1) JP4917613B2 (es)
KR (1) KR20080090464A (es)
CN (1) CN101304980B (es)
AR (1) AR058572A1 (es)
AT (1) ATE519750T1 (es)
AU (1) AU2006331404A1 (es)
BR (1) BRPI0620621A2 (es)
CA (1) CA2633932A1 (es)
IL (1) IL192316A0 (es)
RU (1) RU2008130259A (es)
TW (1) TW200732319A (es)
WO (1) WO2007074130A2 (es)
ZA (1) ZA200802671B (es)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2012171987A1 (en) * 2011-06-16 2012-12-20 Lonza Ltd A process for extraction of peptides and its application in liquid phase peptide synthesis
GB201707938D0 (en) 2017-05-17 2017-06-28 Univ Sheffield Compounds
WO2021218863A1 (zh) * 2020-04-26 2021-11-04 江苏恩华药业股份有限公司 1,5-二氢-2,4-苯二氮䓬-3-酮衍生物及其应用

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3474090A (en) 1966-12-22 1969-10-21 American Cyanamid Co 3-aminoalkyl-1,3-benzodiazepin-2-ones
AU4698399A (en) * 1998-06-30 2000-01-17 Du Pont Pharmaceuticals Company 1,3-benzodiazepin-2-ones and 1,3-benzoxazepin-2-ones useful as hiv reverse transcriptase inhibitors
DE19911039A1 (de) 1999-03-12 2000-09-14 Boehringer Ingelheim Pharma Abgewandelte Aminosäureamide, diese Verbindungen enthaltende Arzneimittel und Verfahren zu ihrer Herstellung
US7220862B2 (en) 2002-06-05 2007-05-22 Bristol-Myers Squibb Company Calcitonin gene related peptide receptor antagonists
EP1689493A4 (en) 2003-12-05 2008-04-23 Bristol Myers Squibb Co ANTAGONISTS OF THE CALCITONIN GENE RELATED PEPTIDE RECEPTOR
EP1619187A1 (de) 2004-07-23 2006-01-25 Boehringer Ingelheim Pharma GmbH & Co. KG Verfahren zur Herstellung von 3-(4-Piperidinyl)- 2,3,4,5-tetrahydro-1,3-benzodiazepin-2(1H)-on

Also Published As

Publication number Publication date
EP1968952B1 (de) 2011-08-10
KR20080090464A (ko) 2008-10-08
CN101304980B (zh) 2011-05-11
WO2007074130A2 (de) 2007-07-05
BRPI0620621A2 (pt) 2011-11-16
AU2006331404A1 (en) 2007-07-05
WO2007074130A3 (de) 2007-08-16
IL192316A0 (en) 2009-02-11
CN101304980A (zh) 2008-11-12
ATE519750T1 (de) 2011-08-15
RU2008130259A (ru) 2010-01-27
JP2009521420A (ja) 2009-06-04
US20080009617A1 (en) 2008-01-10
EP1968952A2 (de) 2008-09-17
CA2633932A1 (en) 2007-07-05
ZA200802671B (en) 2009-01-28
JP4917613B2 (ja) 2012-04-18
US7473778B2 (en) 2009-01-06
TW200732319A (en) 2007-09-01

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