IE35727L - Benzodiazepines. - Google Patents

Benzodiazepines.

Info

Publication number
IE35727L
IE35727L IE700753A IE75370A IE35727L IE 35727 L IE35727 L IE 35727L IE 700753 A IE700753 A IE 700753A IE 75370 A IE75370 A IE 75370A IE 35727 L IE35727 L IE 35727L
Authority
IE
Ireland
Prior art keywords
group
general formula
benzodiazepin
tetrahydro
reaction
Prior art date
Application number
IE700753A
Other versions
IE35727B1 (en
Original Assignee
Boehringer Sohn Ingelheim
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 DE19691929656 external-priority patent/DE1929656A1/en
Priority claimed from DE19702006600 external-priority patent/DE2006600A1/en
Priority claimed from DE19702019627 external-priority patent/DE2019627A1/en
Application filed by Boehringer Sohn Ingelheim filed Critical Boehringer Sohn Ingelheim
Publication of IE35727L publication Critical patent/IE35727L/en
Publication of IE35727B1 publication Critical patent/IE35727B1/en

Links

Classifications

    • 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
    • C07D243/121,5-Benzodiazepines; Hydrogenated 1,5-benzodiazepines

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

1317475 1 H - 2,3,4,5 - Tetrahydro - 1,5- benzodiazepin - 4 - ones BOEHRINGER INGELHEIM GmbH 10 June 1970 [11 June 1969 13 Feb 1970 23 April 1970] 28197/70 Heading C2C Novel 1H - 2,3,4,5 - tetrahydro - 1,5 - benzodiazepin-4-ones of the general formula wherein R 1 is a hydrogen atom or a straight or branched chain C 1-6 alkyl group, an unsaturated aliphatic C 2-6 hydrocarbon group, a C 2-3 alkyl group substituted by a hydroxy group in the terminal position, or a C 4-7 cycloalkylmethyl or formyl group, R 2 is an α-pyridyl group, or a phenyl group optionally substituted in the oposition thereof by a halogen atom or a nitro or trifluoromethyl group and R 3 is a hydrogen or halogen atom or a hydroxy, trifluoromethyl, nitro or cyano group, and, except when R 1 is a formyl group and R 2 is other than an α-pyridyl group, physiologically acceptable acid addition salts thereof are prepared (a) when R 1 is other than a formyl group, by reaction of a 1H-2,3,4,5- tetrahydro - 1,5 - benzodiazepin - 4 - one of the general formula wherein R 4 is as R 1 with the exception of a formyl group, with an aryl or heteroaryl halide of the general formula R 2 X, wherein X is a halogen atom; (b) when R 1 is other than a formyl group, by cyclization of an N-(2-anilinophenyl)-#-alanine of the general formula (c) when R 1 is other than a formyl group, by cyclization of an N-acyl-o-phenylenediamine of the general formula wherein Y is a vinyl or 2-haloethyl group; (d) when R 1 is other than a hydrogen atom, by reaction of a lH-2,3,4,5-tetrahydro-1,5-benzodiazepin-4-one of the general formula with a compound of the general formula R 5 Y, wherein R 5 is as R 1 with the exception of a hydrogen atom and Y is an atom or group readily removable as an anion; (e) when R 1 is a 2-hydroxyethyl group, by reaction of a 1H-2,3,4,5 - tetrahydro - 1,5 - benzodiazepin-4- one of the sixth general formula above with ethylene oxide, and (f) when R 1 is a formyl group, by reaction of a 1H-2,3,4,5-tetrahydro- 1,5 - benzodiazepin - 4 - one of the sixth general formula above with formic acid; followed optionally, where appropriate, by salification of the product. Pharmaceutical compositions having tranquillizing activity comprise, as active ingredient, at least one lH-2,3,4,5-tetrahydro-1,5-benzodiazepin-4-one of the first general formula above or physiologically acceptable acid addition salt thereof, in association with a pharmaceutical carrier or excipient, and may be administered orally, parenterally or rectally. [GB1317475A]
IE753/70A 1969-06-11 1970-06-10 Novel benzodiazepines the preparation thereof and compositions containing the same IE35727B1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE19691929656 DE1929656A1 (en) 1969-06-11 1969-06-11 Tetrahydro-1,5-benzodiazepine-4-ones
DE19702006600 DE2006600A1 (en) 1970-02-13 1970-02-13 Tetrahydro-1,5-benzodiazepine-4-ones
DE19702019627 DE2019627A1 (en) 1969-06-11 1970-04-23 Tetrahydro-1,5-benzodiazepine-4-ones

Publications (2)

Publication Number Publication Date
IE35727L true IE35727L (en) 1970-12-11
IE35727B1 IE35727B1 (en) 1976-05-12

Family

ID=27181978

Family Applications (1)

Application Number Title Priority Date Filing Date
IE753/70A IE35727B1 (en) 1969-06-11 1970-06-10 Novel benzodiazepines the preparation thereof and compositions containing the same

Country Status (16)

Country Link
JP (3) JPS49192B1 (en)
AT (2) AT303746B (en)
BE (1) BE751834A (en)
BG (4) BG17602A3 (en)
CA (1) CA967154A (en)
CH (1) CH549582A (en)
ES (4) ES380557A1 (en)
FR (1) FR2052950B1 (en)
GB (1) GB1317475A (en)
IE (1) IE35727B1 (en)
IL (1) IL34689A (en)
NL (1) NL7008404A (en)
NO (1) NO129524B (en)
RO (4) RO58887A (en)
SE (1) SE381873B (en)
SU (1) SU423299A3 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110183397B (en) * 2019-06-24 2022-08-23 陕西师范大学 Method for preparing 1, 5-benzothiazine compound by catalysis of zirconocene dichloride
CN110256365B (en) * 2019-06-24 2022-06-07 陕西师范大学 Method for preparing benzodiazepine derivative by catalysis of dichlorotitanocene

Also Published As

Publication number Publication date
JPS49192B1 (en) 1974-01-05
ES387138A1 (en) 1973-05-01
NL7008404A (en) 1970-12-15
AT303746B (en) 1972-11-15
CA967154A (en) 1975-05-06
RO58887A (en) 1975-10-15
CH549582A (en) 1974-05-31
ES380557A1 (en) 1973-04-01
RO58405A (en) 1975-11-15
JPS5031158B1 (en) 1975-10-07
BG17974A3 (en) 1974-03-05
IL34689A (en) 1973-03-30
BG17603A3 (en) 1973-11-10
BG17973A3 (en) 1974-03-05
GB1317475A (en) 1973-05-16
SE381873B (en) 1975-12-22
SU423299A3 (en) 1974-04-05
ES387136A1 (en) 1974-01-01
FR2052950A1 (en) 1971-04-16
BE751834A (en) 1970-12-11
JPS5013273B1 (en) 1975-05-19
RO58641A (en) 1975-09-15
ES387137A1 (en) 1974-01-01
RO58640A (en) 1975-10-15
IE35727B1 (en) 1976-05-12
FR2052950B1 (en) 1974-08-30
NO129524B (en) 1974-04-22
BG17602A3 (en) 1973-11-10
IL34689A0 (en) 1970-08-19
AT303737B (en) 1972-12-11

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