PL90606B1 - - Google Patents

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Publication number
PL90606B1
PL90606B1 PL1971176135A PL17613571A PL90606B1 PL 90606 B1 PL90606 B1 PL 90606B1 PL 1971176135 A PL1971176135 A PL 1971176135A PL 17613571 A PL17613571 A PL 17613571A PL 90606 B1 PL90606 B1 PL 90606B1
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PL
Poland
Prior art keywords
group
general formula
compound
carbon atoms
hydrogen
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Application number
PL1971176135A
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Polish (pl)
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Publication of PL90606B1 publication Critical patent/PL90606B1/pl

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D243/00Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms
    • C07D243/06Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4
    • C07D243/10Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
    • C07D243/141,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines
    • C07D243/161,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines substituted in position 5 by aryl radicals
    • C07D243/181,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines substituted in position 5 by aryl radicals substituted in position 2 by nitrogen, oxygen or sulfur atoms
    • C07D243/24Oxygen atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/22Anxiolytics

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (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)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)

Claims (3)

Zastrzezenia patentowe 1. Sposób wytwarzania nowych pochodnych benzodiazepiny o ogólnym wzorze 1, w którym Rt oznacza grupe cyjanowa, R2 oznacza grupe pirydylowa lub grupe o ogólnym wzorze 2, w którym R5 i R6 sa jednakowa lub rózne i oznaczaja atomy wodoru, atomy chlorowca, rodniki alkilowe o 1—4 atomach wegla lub rodniki trójfluorometylowe, R3 oznacza atom wodoru, rodnik alkilowy o 1—4 atomach wegla lub rodnik aralkilowy, R4 oznacza grupe czterowodoropiranyloksylowa, czterowodorofuranyloksylowa, aryloksylowa, aralkoksylowa lub alkoksyalkoksylowa, m oznacza zero lub 1, a n oznacza liczbe calkowita 1-4, albo soli addycyjnych tych zwiazków z kwasami, znamienny tym, ze zwiazek o ogólnym wzorze 3, w którym Ri, R2, R3, R4 i n maja wyzej podane znaczenie, albo addycyjna sól tego zwiazku z kwasem, poddaje sie reakcji z srodkiem utleniajacym. .Claims 1. A method for the preparation of new benzodiazepine derivatives of the general formula 1, in which Rt is a cyano group, R2 is a pyridyl group or a group of the general formula 2, in which R5 and R6 are the same or different and represent hydrogen atoms, halogen atoms, radicals alkyl with 1-4 carbon atoms or trifluoromethyl radicals, R3 is hydrogen, alkyl group with 1-4 carbon atoms or aralkyl radical, R4 is tetrahydropiranyloxy, tetrahydrofuranyloxy, aryloxy, aralkoxy or alkoxyalkoxy groups, and m is zero or 1, the total of 1-4, or acid addition salts of these compounds, characterized in that a compound of the general formula in which R1, R2, R3, R4 and n are as defined above, or an acid addition salt of this compound is reacted with an oxidizing agent. . 2. Sposób, wedlug zastrz. 1, znamienny tym, ze jako srodek utleniajacy stosuje sie ozon, kwas chromowy, nadtlenek wodoru, kwas nadtlenowy lub nadmanganian potasu.2. The method according to claim The process of claim 1, wherein the oxidizing agent is ozone, chromic acid, hydrogen peroxide, peroxy acid or potassium permanganate. 3. Sposób wytwarzania nowych pochodnych benzodiazepiny o ogólnym wzorze 1, w którym Ri oznacza atom wodoru, atom chlorowca, grupe nitrowa, grupe a IkoksyIowa o 1—4 atomach wegla lub grupe trójfluorome- tylowa, R2 oznacza grupe pirydylowa lub grupe o ogólnym wzorze 2, w którym R5 i R6 sa jednakowe lub rózne i oznaczaja atomy wodoru, atomy chlorowca, rodniki alkilowe o 1—4 atomach wegla lub rodniki.trójfluoromety¬ lowe, R3 oznacza atom wodoru, R oznacza grupe czterowodoropiranyloksyIowa, aryloksyIowa, aralkoksylowa lub alkoksyalkoksylowa, m oznacza zero, a n oznacza liczbe calkowita 1-4, albo addycyjnych soli tych zwiazków z kwasami, znamienny tym, ze zwiazek o ogólnym wzorze 3, w którym Ri, R2, R3 * R4 ¦ n maja wyzej podane znaczenie, albo addycyjna sól tego zwiazku z kwasem, poddaje sie reakcji ze srodkiem utleniajacym.90 606 * CnH2n n N-cr ^CH-R, R2 (o)m Wzór 1 Wzór 2 R Ctó 2 ki^ CH-NH2 N i l I R3 yn'~'2n Ra Wzór 3 Prac. Poligraf. UP PRL naklad 120+18 Cena 10 zl PL3. Process for the preparation of new benzodiazepine derivatives of the general formula I, in which R 1 represents a hydrogen atom, a halogen atom, a nitro group, a Ikoxy group of 1-4 carbon atoms or a trifluoromethyl group, R2 is a pyridyl group or a group of the general formula II in which R5 and R6 are the same or different and represent hydrogen atoms, halogen atoms, alkyl radicals with 1-4 carbon atoms or trifluoromethyl radicals, R3 is hydrogen, R is tetrahydro pyranyloxy, aryloxy, aralkoxy or alkoxyalkoxy groups, is zero, and n is the integer of 1-4, or acid addition salts of these compounds, characterized in that a compound of general formula 3, in which R1, R2, R3 * R4 4n have the meaning given above, or an addition salt of this compound with acid, reacted with an oxidizing agent. 90 606 * CnH2n n N-cr ^ CH-R, R2 (o) m Formula 1 Formula 2 R Ctó 2 ki ^ CH-NH2 N il I R3 yn '~' 2n Ra Model 3 of the Works. Typographer. UP PRL, circulation 120 + 18 Price PLN 10 PL
PL1971176135A 1970-08-31 1971-08-31 PL90606B1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP45076545A JPS4843359B1 (en) 1970-08-31 1970-08-31

Publications (1)

Publication Number Publication Date
PL90606B1 true PL90606B1 (en) 1977-01-31

Family

ID=13608222

Family Applications (1)

Application Number Title Priority Date Filing Date
PL1971176135A PL90606B1 (en) 1970-08-31 1971-08-31

Country Status (5)

Country Link
JP (1) JPS4843359B1 (en)
AT (1) AT312619B (en)
CH (1) CH583206A5 (en)
PL (1) PL90606B1 (en)
SU (1) SU618042A3 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2697454C (en) * 2007-08-29 2015-11-03 Schering Corporation 2-carboxy substituted indole derivatives and methods of use thereof

Also Published As

Publication number Publication date
CH583206A5 (en) 1976-12-31
AT312619B (en) 1973-12-15
JPS4843359B1 (en) 1973-12-18
SU618042A3 (en) 1978-07-30

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