ES8104806A1 - Un procedimiento para la preparacion de octahidro-1h-pirro- lo-(2,3g)isoquinolinas - Google Patents

Un procedimiento para la preparacion de octahidro-1h-pirro- lo-(2,3g)isoquinolinas

Info

Publication number
ES8104806A1
ES8104806A1 ES493015A ES493015A ES8104806A1 ES 8104806 A1 ES8104806 A1 ES 8104806A1 ES 493015 A ES493015 A ES 493015A ES 493015 A ES493015 A ES 493015A ES 8104806 A1 ES8104806 A1 ES 8104806A1
Authority
ES
Spain
Prior art keywords
alkyl
hydroxy
phenyl
alkoxy
alkylamino
Prior art date
Legal status (The legal status 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 status listed.)
Expired
Application number
ES493015A
Other languages
English (en)
Other versions
ES493015A0 (es
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
F Hoffmann La Roche AG
Original Assignee
F Hoffmann La Roche 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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=26754910&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=ES8104806(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority claimed from US06/073,813 external-priority patent/US4260762A/en
Application filed by F Hoffmann La Roche AG filed Critical F Hoffmann La Roche AG
Publication of ES493015A0 publication Critical patent/ES493015A0/es
Publication of ES8104806A1 publication Critical patent/ES8104806A1/es
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/18Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • 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
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/08Indoles; Hydrogenated indoles with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to carbon atoms of the hetero ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D217/00Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
    • C07D217/02Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines
    • C07D217/04Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines with hydrocarbon or substituted hydrocarbon radicals attached to the ring nitrogen atom
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/55Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Medicinal Chemistry (AREA)
  • Psychiatry (AREA)
  • Neurology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Biomedical Technology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Neurosurgery (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

PROCEDIMIENTO PARA LA PREPARACION DE OCTAHIDRO-1H-PIRROLO[2-3-G]ISOQUINOLINAS DE FORMULA GENERAL (I). CONSISTENTE EN OBTENER EL COMPUESTO (I) SUS ISOMEROS OPTICOS Y GEOMETRICOS Y SUS SALES DE ADICION DE ACIDO FARMACEUTICAMENTE ACEPTABLES, POR REACCION DE UNA DIHIDRO-INDOLONA-ETILAMINA, DE FORMULA GENERAL (II), CON FORMALDEHIDO, EN CUYAS FORMULAS GENERAL R2 Y R3 SON, INDEPENDIENTEMENTE, HIDROGENO, ALQUILO, CICLOALQUILO, ALQUENILO, ACILO, ARILO O ARALQUILO; R4 ES ALQUILO, ALCOXIALQUILO O ALQUIL-CICLOALQUILO. LA REACCION TIENE LUGAR EN MEDIO DISOLVENTE INERTE, A TEMPERATURA DE 135 A 200GC. LOS COMPUESTOS DE FORMULA GENERAL (I) PUEDEN UTILIZARSE COMO AGENTES ANTIPSICOTICOS, POR EL EJEMPLO, EN EL TRATAMIENTO DE LA ESQUIZOFRENIA. *FORMULA* D
ES493015A 1978-10-13 1980-07-02 Un procedimiento para la preparacion de octahidro-1h-pirro- lo-(2,3g)isoquinolinas Expired ES8104806A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US95094778A 1978-10-13 1978-10-13
US06/073,813 US4260762A (en) 1979-09-10 1979-09-10 Octahydro-1H-pyrrolo[2,3-g]isoquinolines

Publications (2)

Publication Number Publication Date
ES493015A0 ES493015A0 (es) 1981-05-16
ES8104806A1 true ES8104806A1 (es) 1981-05-16

Family

ID=26754910

Family Applications (2)

Application Number Title Priority Date Filing Date
ES493015A Expired ES8104806A1 (es) 1978-10-13 1980-07-02 Un procedimiento para la preparacion de octahidro-1h-pirro- lo-(2,3g)isoquinolinas
ES493014A Expired ES8104805A1 (es) 1978-10-13 1980-07-02 Un procedimiento para la preparacion de octahidro-1h-pirro- lo-(2,3g)isoquinolinas

Family Applications After (1)

Application Number Title Priority Date Filing Date
ES493014A Expired ES8104805A1 (es) 1978-10-13 1980-07-02 Un procedimiento para la preparacion de octahidro-1h-pirro- lo-(2,3g)isoquinolinas

Country Status (18)

Country Link
EP (1) EP0010661B1 (es)
AR (2) AR228244A1 (es)
AU (1) AU528685B2 (es)
CA (1) CA1132553A (es)
CS (1) CS242858B2 (es)
DE (1) DE2967215D1 (es)
DK (1) DK430579A (es)
ES (2) ES8104806A1 (es)
FI (1) FI67548C (es)
HU (1) HU181883B (es)
IE (1) IE48965B1 (es)
IL (1) IL58438A (es)
MC (1) MC1285A1 (es)
NO (1) NO152873C (es)
NZ (1) NZ191830A (es)
PH (1) PH14835A (es)
PT (1) PT70310A (es)
SU (3) SU1014474A3 (es)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MC1377A1 (fr) * 1980-02-28 1982-01-19 Hoffmann La Roche Derives d'isoquinoleine
DE3363146D1 (en) * 1982-03-29 1986-05-28 Hoffmann La Roche Process for the manufacture of isoquinoline diones
US4732902A (en) * 1986-05-23 1988-03-22 Hoffmann-La Roche Inc. Pyrroloisoquinolinyl-dimethyloxoalkyl alkonoates and their use as antipsychotic agents
GB8828669D0 (en) * 1988-12-08 1989-01-11 Lilly Industries Ltd Organic compounds
EP1131284A1 (de) 1998-11-20 2001-09-12 Basf Aktiengesellschaft Verfahren und zwischenprodukte zur herstellung von bis(oxim)monoethern

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS51118799A (en) * 1975-04-10 1976-10-18 Sankyo Co Ltd Method for preparing pyridindole derivatives

Also Published As

Publication number Publication date
MC1285A1 (fr) 1980-07-22
PT70310A (en) 1979-11-01
ES493014A0 (es) 1981-05-16
EP0010661B1 (de) 1984-09-12
ES493015A0 (es) 1981-05-16
SU1109052A3 (ru) 1984-08-15
NZ191830A (en) 1984-09-28
EP0010661A3 (en) 1980-10-01
ES8104805A1 (es) 1981-05-16
NO152873C (no) 1985-12-04
FI793183A (fi) 1980-04-14
AR228244A1 (es) 1983-02-15
FI67548B (fi) 1984-12-31
NO152873B (no) 1985-08-26
SU1048985A3 (ru) 1983-10-15
EP0010661A2 (de) 1980-05-14
HU181883B (en) 1983-11-28
IE48965B1 (en) 1985-06-26
IL58438A (en) 1982-12-31
IE791944L (en) 1980-04-13
CA1132553A (en) 1982-09-28
IL58438A0 (en) 1980-01-31
AU528685B2 (en) 1983-05-12
CS694579A2 (en) 1985-08-15
PH14835A (en) 1981-12-16
AR229096A1 (es) 1983-06-15
FI67548C (fi) 1985-04-10
NO793301L (no) 1980-04-15
SU1014474A3 (ru) 1983-04-23
CS242858B2 (en) 1986-05-15
AU5169779A (en) 1980-04-17
DK430579A (da) 1980-04-14
DE2967215D1 (en) 1984-10-18

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