MX3393E - PROCEDURE FOR THE PREPARATION OF ARYALCOHYLAMINES - Google Patents

PROCEDURE FOR THE PREPARATION OF ARYALCOHYLAMINES

Info

Publication number
MX3393E
MX3393E MX000041U MX4176U MX3393E MX 3393 E MX3393 E MX 3393E MX 000041 U MX000041 U MX 000041U MX 4176 U MX4176 U MX 4176U MX 3393 E MX3393 E MX 3393E
Authority
MX
Mexico
Prior art keywords
signifies
group
hydrogen atom
general formula
hydrogen
Prior art date
Application number
MX000041U
Other languages
Spanish (es)
Inventor
Wolfgang Eberlein
Ederhard Kutter
Joachin Neider
Original Assignee
Karl Thomas Ges Nit Bescharank
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
Priority claimed from DE2509797A external-priority patent/DE2509797C2/en
Priority claimed from DE19752558274 external-priority patent/DE2558274A1/en
Priority claimed from DE19752558273 external-priority patent/DE2558273A1/en
Application filed by Karl Thomas Ges Nit Bescharank filed Critical Karl Thomas Ges Nit Bescharank
Publication of MX3393E publication Critical patent/MX3393E/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/44Iso-indoles; Hydrogenated iso-indoles
    • C07D209/48Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/06Antiarrhythmics
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C309/00Sulfonic acids; Halides, esters, or anhydrides thereof
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/44Iso-indoles; Hydrogenated iso-indoles
    • C07D209/46Iso-indoles; Hydrogenated iso-indoles with an oxygen atom in position 1
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D275/00Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings
    • C07D275/04Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings condensed with carbocyclic rings or ring systems
    • C07D275/06Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings condensed with carbocyclic rings or ring systems with hetero atoms directly attached to the ring sulfur atom

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Cardiology (AREA)
  • Chemical Kinetics & Catalysis (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)
  • Heart & Thoracic Surgery (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Indole Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

La presente invención se refiere a un procedimiento para la preparación de arilalcohilaminas substituídas de la fórmula general I: (VER FIGURA) en la que R1 significa un átomo de hidrógeno; R2 significa un átomo de hidrógeno, un átomo de cloro o el grupo metoxi; R3 significa un átomo de hidrógeno o el grupo metoxi, o conjuntamente con R2 el grupo metilendioxi o etilendioxi; R4 y R5, que pueden ser iguales o diferentes, significan átomos de hidrógeno o grupos alcohilo inferior; R6 significa un átomo de hidrógeno o un grupo alcoxi inferior; R7 significa un grupo alcoxi inferior o conjuntamente con R6 el grupo metilendioxi o etilendioxi; X significa el grupo carbonilo; y n significa el número 2 ó 3, así como sus sales por adición de ácido fisiológicamente compatibles con ácidos orgánicos o inorgánicos, caracterizado porque se reduce un compuesto de la fórmula general II: (VER FIGURA) con hidrógeno naciente o activado catalíticamente en un disolvente y a temperaturas comprendidas entre 0 y 250°C, y, en caso deseado, un compuesto obtenido de la fórmula general I se transforma en una sal por adición de ácido, con un ácido orgánico o inorgánico.The present invention relates to a process for the preparation of substituted arylalcohilamines of the general formula I: (SEE FIGURE) in which R1 signifies a hydrogen atom; R2 signifies a hydrogen atom, a chlorine atom or the methoxy group; R3 signifies a hydrogen atom or the methoxy group, or together with R2 the methylenedioxy or ethylenedioxy group; R4 and R5, which may be the same or different, signify hydrogen atoms or lower alcohol groups; R6 signifies a hydrogen atom or a lower alkoxy group; R7 means a lower alkoxy group or together with R6 the methylenedioxy or ethylenedioxy group; X signifies the carbonyl group; and n means the number 2 or 3, as well as its acid addition salts physiologically compatible with organic or inorganic acids, characterized in that a compound of the general formula II is reduced: (SEE FIGURE) with nascent or catalytically activated hydrogen in a solvent already temperatures between 0 and 250 ° C, and, if desired, a compound obtained of the general formula I is transformed into an acid addition salt, with an organic or inorganic acid.

MX000041U 1975-03-06 1976-03-05 PROCEDURE FOR THE PREPARATION OF ARYALCOHYLAMINES MX3393E (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE2509797A DE2509797C2 (en) 1975-03-06 1975-03-06 Phthalimidines, their physiologically acceptable acid addition salts, processes for their preparation and pharmaceuticals containing these compounds
DE19752558274 DE2558274A1 (en) 1975-12-23 1975-12-23 N-substd. phthalimidines and benzo isothiazolines - for coronary insufficiency and angina pectoris
DE19752558273 DE2558273A1 (en) 1975-12-23 1975-12-23 NEW PROCESSES FOR THE PRODUCTION OF ARYLALKYLAMINES

Publications (1)

Publication Number Publication Date
MX3393E true MX3393E (en) 1980-10-28

Family

ID=27186298

Family Applications (1)

Application Number Title Priority Date Filing Date
MX000041U MX3393E (en) 1975-03-06 1976-03-05 PROCEDURE FOR THE PREPARATION OF ARYALCOHYLAMINES

Country Status (22)

Country Link
JP (1) JPS51113866A (en)
AU (1) AU498958B2 (en)
CA (1) CA1073915A (en)
CH (1) CH621340A5 (en)
DD (1) DD123741A5 (en)
DK (1) DK138792C (en)
ES (1) ES445812A1 (en)
FI (1) FI61694C (en)
FR (1) FR2302733A1 (en)
GB (1) GB1503625A (en)
GR (1) GR60053B (en)
HK (1) HK46881A (en)
IE (1) IE42962B1 (en)
IL (1) IL49150A (en)
LU (1) LU74479A1 (en)
MX (1) MX3393E (en)
NL (1) NL7601796A (en)
NO (1) NO144212C (en)
PT (1) PT64873B (en)
SE (1) SE418398B (en)
SU (1) SU620209A3 (en)
YU (3) YU40642B (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3242477A1 (en) * 1982-11-18 1984-05-24 Basf Ag, 6700 Ludwigshafen HETEROCYCLICALLY SUBSTITUTED NITRILES, THEIR PRODUCTION AND USE AS MEDICINAL PRODUCTS
GB8609331D0 (en) * 1986-04-16 1986-05-21 Pfizer Ltd Anti-arrythmia agents
US5567718A (en) * 1994-08-11 1996-10-22 Hoechst Marion Roussel Inc. 2,3-dihydro-1h-isoindole derivatives and their use as serotonin reuptake inhibitors
DE60114413T2 (en) 2000-05-25 2006-07-27 F. Hoffmann-La Roche Ag SUBSTITUTED 1-AMINOALKYL-LACTAME AND THEIR USE AS MUSCARIN RECEPTOR ANTAGONISTS

Also Published As

Publication number Publication date
YU55076A (en) 1982-08-31
CA1073915A (en) 1980-03-18
IL49150A (en) 1978-12-17
NO760766L (en) 1976-09-07
JPS51113866A (en) 1976-10-07
YU40642B (en) 1986-04-30
DK138792C (en) 1979-04-02
SE7602856L (en) 1976-09-07
IE42962L (en) 1976-09-06
PT64873A (en) 1976-04-01
SE418398B (en) 1981-05-25
DK138792B (en) 1978-10-30
DK92876A (en) 1976-09-07
DD123741A5 (en) 1977-01-12
PT64873B (en) 1978-02-06
FI61694C (en) 1982-09-10
FI61694B (en) 1982-05-31
NL7601796A (en) 1976-09-08
GB1503625A (en) 1978-03-15
NO144212B (en) 1981-04-06
IL49150A0 (en) 1976-05-31
AU498958B2 (en) 1979-03-29
FR2302733A1 (en) 1976-10-01
AU1172976A (en) 1977-09-08
JPS6139305B2 (en) 1986-09-03
FR2302733B1 (en) 1979-09-21
YU98082A (en) 1986-04-30
HK46881A (en) 1981-09-25
NO144212C (en) 1981-07-15
ES445812A1 (en) 1977-06-16
LU74479A1 (en) 1977-09-27
YU98182A (en) 1986-04-30
IE42962B1 (en) 1980-11-19
SU620209A3 (en) 1978-08-15
CH621340A5 (en) 1981-01-30
GR60053B (en) 1978-04-04
FI760465A (en) 1976-09-07

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