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ES412107A1 - Procedure for the obtaining of new diazepine derivatives. (Machine-translation by Google Translate, not legally binding) - Google Patents

Procedure for the obtaining of new diazepine derivatives. (Machine-translation by Google Translate, not legally binding)

Info

Publication number
ES412107A1
ES412107A1 ES412107A ES412107A ES412107A1 ES 412107 A1 ES412107 A1 ES 412107A1 ES 412107 A ES412107 A ES 412107A ES 412107 A ES412107 A ES 412107A ES 412107 A1 ES412107 A1 ES 412107A1
Authority
ES
Spain
Prior art keywords
formula
group
carbon atoms
indicated
substituted
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
ES412107A
Other languages
Spanish (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.)
Novartis AG
Original Assignee
Ciba Geigy 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
Priority claimed from DK560071AA external-priority patent/DK138854B/en
Priority claimed from CH291772A external-priority patent/CH567509A5/en
Application filed by Ciba Geigy AG filed Critical Ciba Geigy AG
Publication of ES412107A1 publication Critical patent/ES412107A1/en
Expired legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/551Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
    • A61K31/55131,4-Benzodiazepines, e.g. diazepam or clozapine
    • A61K31/55171,4-Benzodiazepines, e.g. diazepam or clozapine condensed with five-membered rings having nitrogen as a ring hetero atom, e.g. imidazobenzodiazepines, triazolam
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (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)

Abstract

Procedure for obtaining new diazepine derivatives of general formula I **(See formula)** where R1 signifies hydrogen or an alkyl group with 3 carbon atoms, A signifies an alkylene group with 1 to 3 carbon atoms, R2 signifies the hydroxyl group, an alkoxy group with 1 to 6 carbon atoms, a mono group - or diaryl-methoxy, a dialkylamino, N-alkyl-aralkylamino or diaraiquilamino group, where the alkyl groups contain 1 to 6 and the aralkyl groups 7 to 9 carbon atoms, a polymethylenimino residue with 5 to 7 ring members or a residue morpholino, the cyclic moieties of which may be substituted by alkyl groups including these contain a maximum of 10 carbon atoms, or R2-A together signify a dialkoxymethyl group, whose alkoxy moieties contain 1 to 4 carbon atoms, or an alkylenedioxymethyl group with a total of 3 carbon atoms and rings B and C can be substituted by halogen up to atomic number 35, trifluoromethyl, alkyl or alkoxy groups with 1 to 6 carbon atoms, and their addition salts with inorganic or organic acids, ca characterized by a compound of general formula **(See formula)** where R'2 has the indicated meaning for R2, in formula 1, with the exception of the hydroxyl group, R1, A or R'2-A have the indicated meanings for R1, A or R2-A under the formula I and ring B can be substituted as indicated therein, or a metal derivative thereof, is reacted with a compound of general formula III **(See formula)** wherein Hal means bromine or iodine and ring C may be substituted as indicated under formula I, and, if desired, a reaction product obtained from general formula Ia, comprised within formula I, **(See formula)** wherein R'2 signifies a monoarylmethoxy or diarylmethoxy group, while R1 and A have the meaning indicated under formula I and rings B and 0 may be substituted as indicated therein, dissociates a compound of formula I, the residue R2 is the hydroxyl group, and/or, if desired, a compound of general formula la or I is transformed into an addition salt with an inorganic or organic acid. (Machine-translation by Google Translate, not legally binding)
ES412107A 1971-11-15 1973-02-27 Procedure for the obtaining of new diazepine derivatives. (Machine-translation by Google Translate, not legally binding) Expired ES412107A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DK560071AA DK138854B (en) 1970-11-23 1971-11-15 Analogous process for the preparation of s-triazolo (4,3-a) (1,4) benzodiazepine derivatives or 5-oxides or salts thereof.
CH291772A CH567509A5 (en) 1972-02-29 1972-02-29 Diazepin derivs - prepd from triazolobenzodiazepinones and phenylmagnesiumhalide are central depressants, tranquillisers and
DK248872AA DK140988B (en) 1971-11-15 1972-05-18 Analogous process for the preparation of an s-triazolo (4,3-a) (1,4) benzodiazepine derivatives.

Publications (1)

Publication Number Publication Date
ES412107A1 true ES412107A1 (en) 1976-06-16

Family

ID=27174020

Family Applications (1)

Application Number Title Priority Date Filing Date
ES412107A Expired ES412107A1 (en) 1971-11-15 1973-02-27 Procedure for the obtaining of new diazepine derivatives. (Machine-translation by Google Translate, not legally binding)

Country Status (6)

Country Link
JP (1) JPS5619353B2 (en)
DK (1) DK140988B (en)
ES (1) ES412107A1 (en)
FI (1) FI53821C (en)
PL (1) PL89263B1 (en)
SE (1) SE415101B (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA1234810A (en) * 1983-12-19 1988-04-05 Steve Nichols Non-hygroscopic adinazolam methanesulfonate salt and process therefor

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3987052A (en) * 1969-03-17 1976-10-19 The Upjohn Company 6-Phenyl-4H-s-triazolo[4,3-a][1,4]benzodiazepines

Also Published As

Publication number Publication date
FI53821B (en) 1978-05-02
JPS4892399A (en) 1973-11-30
JPS5619353B2 (en) 1981-05-07
SE415101B (en) 1980-09-08
DK140988B (en) 1979-12-17
PL89263B1 (en) 1976-11-30
FI53821C (en) 1978-08-10
DK140988C (en) 1980-06-02

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