MX3366E - PROCEDURE FOR THE PREPARATION OF OMEGA ACIDS- (6,11-DIHIDRO-11-OXODIBENZ (B, E,) OXEPIN-2-IL) - ALKANOIC - Google Patents

PROCEDURE FOR THE PREPARATION OF OMEGA ACIDS- (6,11-DIHIDRO-11-OXODIBENZ (B, E,) OXEPIN-2-IL) - ALKANOIC

Info

Publication number
MX3366E
MX3366E MX002107U MX210776U MX3366E MX 3366 E MX3366 E MX 3366E MX 002107 U MX002107 U MX 002107U MX 210776 U MX210776 U MX 210776U MX 3366 E MX3366 E MX 3366E
Authority
MX
Mexico
Prior art keywords
alcohol
oxodibenz
oxepin
preparation
alkanoic
Prior art date
Application number
MX002107U
Other languages
Spanish (es)
Inventor
Arthur Raymond Mcfadden
Daniel Eugene Aultz
Original Assignee
Hoechst Ag
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 Hoechst Ag filed Critical Hoechst Ag
Publication of MX3366E publication Critical patent/MX3366E/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D313/00Heterocyclic compounds containing rings of more than six members having one oxygen atom as the only ring hetero atom
    • C07D313/02Seven-membered rings
    • C07D313/06Seven-membered rings condensed with carbocyclic rings or ring systems
    • C07D313/10Seven-membered rings condensed with carbocyclic rings or ring systems condensed with two six-membered rings
    • C07D313/12[b,e]-condensed
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pain & Pain Management (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Biomedical Technology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Rheumatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pyrane Compounds (AREA)

Abstract

La presente invención se refiere a un procedimiento para la preparación de ácidos omega-(6,11-dihidro-11-oxodibenz[b,e]oxepin-2-il)-alcanóicos de la fórmula I (VER FIGURA) donde R es hidrógeno o alcohilo de desde 1 a 4 átomos de carbono, alcohilo de desde 1 a 4 átomos de carbono, o trifluorometilo, y n es un número entero igual a 1, 2 ó 3, o una sal del mismo farmacéuticamente aceptable, que comprende ciclizar un ácido dicarboxílico de la fórmula (VER FIGURA) en donde R' y n son como se definió anteriormente, mediante tratamiento con un medio deshidratante a una temperatura de desde 50 a 125°C y, si se desea, esirificar el compuesto de la fórmula I, en donde R es hidrógeno, haciéndolo reaccionar con un alcohol en la presencia de un ácido, a una temperatura de desde 50°C hasta el punto de ebullición del alcohol.The present invention relates to a process for the preparation of omega- (6,11-dihydro-11-oxodibenz [b, e] oxepin-2-yl) -alkanoic acids of the formula I (SEE FIGURE) where R is hydrogen or alcohol of from 1 to 4 carbon atoms, alcohol of from 1 to 4 carbon atoms, or trifluoromethyl, and n is an integer equal to 1, 2 or 3, or a pharmaceutically acceptable salt thereof, comprising cyclizing an acid dicarboxylic of the formula (SEE FIGURE) where R 'and n are as previously defined, by treatment with a dehydrating medium at a temperature of from 50 to 125 ° C and, if desired, esirify the compound of formula I, in where R is hydrogen, reacting it with an alcohol in the presence of an acid, at a temperature of from 50 ° C to the boiling point of the alcohol.

MX002107U 1975-07-30 1976-07-29 PROCEDURE FOR THE PREPARATION OF OMEGA ACIDS- (6,11-DIHIDRO-11-OXODIBENZ (B, E,) OXEPIN-2-IL) - ALKANOIC MX3366E (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US60021075A 1975-07-30 1975-07-30

Publications (1)

Publication Number Publication Date
MX3366E true MX3366E (en) 1980-10-15

Family

ID=24402733

Family Applications (1)

Application Number Title Priority Date Filing Date
MX002107U MX3366E (en) 1975-07-30 1976-07-29 PROCEDURE FOR THE PREPARATION OF OMEGA ACIDS- (6,11-DIHIDRO-11-OXODIBENZ (B, E,) OXEPIN-2-IL) - ALKANOIC

Country Status (23)

Country Link
JP (1) JPS5217487A (en)
AT (1) AT359066B (en)
AU (1) AU512130B2 (en)
BE (1) BE844728A (en)
CA (1) CA1088078A (en)
CH (1) CH627752A5 (en)
DE (1) DE2629569A1 (en)
DK (1) DK342476A (en)
ES (1) ES450125A1 (en)
FI (1) FI63569C (en)
FR (1) FR2319339A1 (en)
GB (1) GB1560629A (en)
GR (1) GR70328B (en)
HU (1) HU178243B (en)
IE (1) IE43583B1 (en)
IL (1) IL50155A (en)
LU (1) LU75491A1 (en)
MX (1) MX3366E (en)
NL (1) NL7608203A (en)
NO (1) NO147561C (en)
PT (1) PT65421B (en)
SE (1) SE426320B (en)
ZA (1) ZA764557B (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5008285A (en) * 1984-04-27 1991-04-16 Hoechst-Roussel Pharmaceuticals, Inc. (6,11-dihydro-11-oxodibenz[b,e]oxepin-yl)pentanoic acids and derivatives thereof
DE3573256D1 (en) * 1984-04-27 1989-11-02 Hoechst Roussel Pharma (6,11-dihydro-11-oxodibenz(b,e)oxepinyl)pentanoic acids and derivatives, a process and intermediates for their preparation and their use as medicaments

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2138257B1 (en) * 1971-05-21 1974-08-23 Roussel Uclaf
YU204274A (en) * 1973-07-24 1982-06-30 Hoechst Ag Process for preparing new dibenzoxepin derivatives

Also Published As

Publication number Publication date
CH627752A5 (en) 1982-01-29
AU1636376A (en) 1978-02-02
NO762647L (en) 1977-02-01
DK342476A (en) 1977-01-31
SE7608546L (en) 1977-01-31
FI63569B (en) 1983-03-31
GR70328B (en) 1982-09-15
AU512130B2 (en) 1980-09-25
ZA764557B (en) 1977-07-27
AT359066B (en) 1980-10-27
FI762154A (en) 1977-01-31
CA1088078A (en) 1980-10-21
NO147561C (en) 1983-05-04
IL50155A0 (en) 1976-09-30
IE43583L (en) 1977-01-30
ES450125A1 (en) 1977-09-16
BE844728A (en) 1977-01-31
NO147561B (en) 1983-01-24
GB1560629A (en) 1980-02-06
FI63569C (en) 1983-07-11
PT65421A (en) 1976-08-01
IL50155A (en) 1979-12-30
DE2629569A1 (en) 1977-03-31
LU75491A1 (en) 1977-04-15
NL7608203A (en) 1977-02-01
HU178243B (en) 1982-04-28
FR2319339A1 (en) 1977-02-25
JPS5217487A (en) 1977-02-09
ATA559976A (en) 1980-03-15
SE426320B (en) 1982-12-27
PT65421B (en) 1978-04-05
IE43583B1 (en) 1981-04-08
FR2319339B1 (en) 1978-11-17

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