GB1365455A - Imdazobensodiazepines - Google Patents

Imdazobensodiazepines

Info

Publication number
GB1365455A
GB1365455A GB4627872A GB4627872A GB1365455A GB 1365455 A GB1365455 A GB 1365455A GB 4627872 A GB4627872 A GB 4627872A GB 4627872 A GB4627872 A GB 4627872A GB 1365455 A GB1365455 A GB 1365455A
Authority
GB
United Kingdom
Prior art keywords
alkyl
imidazobenzodiazepines
alkenyl
prepared
tranquillizers
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
GB4627872A
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.)
Pharmacia and Upjohn Co
Original Assignee
Upjohn Co
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
Application filed by Upjohn Co filed Critical Upjohn Co
Publication of GB1365455A publication Critical patent/GB1365455A/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P21/00Drugs for disorders of the muscular or neuromuscular system
    • A61P21/02Muscle relaxants, e.g. for tetanus or cramps
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/08Antiepileptics; Anticonvulsants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/20Hypnotics; Sedatives

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Neurology (AREA)
  • Public Health (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Pain & Pain Management (AREA)
  • Anesthesiology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Fodder In General (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

1365455 Imidazobenzodiazepines UPJOHN CO 6 Oct 1972 [2 Nov 1971] 46278/72 Heading C2C Imidazobenzodiazepines are prepared by the following route (R = H, C 1-4 alkyl, C 3-4 alkenyl; R 1 = H, C 1-3 alkyl; R 2 = 2, 3 or 4-Py, 2-pyrimidyl, furyl, pyrryl, thienyl, C 1-3 alkyl, C 2-4 alkenyl, C 5-7 cycloalkyl or cycloalkenyl, R 3 R 4 Ph; R 3,4 = H, halogen, NO 2 , CN, CF 3 , C 1-3 alkyl, alkoxy, alkylthio; alkylsulphinyl, alkylsulphonyl or alkanoylamino, di(C 1-3 alkyl)amino; X = F, Cl, Br), optionally followed by conversion to an acid addition salt. The starting materials are prepared by heating the corresponding 1,3-dihydro-2H-1,4-benzodiazepin-2-one with phosphorus pentasulphide, and reacting the resulting 2-thione with RNH 2 . The above compounds are sedatives, hypnotics, anticonvulsants, tranquillizers and muscle relaxants, and increase growth rate, feed efficiency and milk and egg production in livestock. They may be administered in the form of pharmaceutical and veterinary preparations and feed additives containing them in association with a carrier.
GB4627872A 1971-11-02 1972-10-06 Imdazobensodiazepines Expired GB1365455A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US19504971A 1971-11-02 1971-11-02
US00364616A US3846443A (en) 1971-11-02 1973-05-29 1H-IMIDAZO{8 1,2a{9 {8 1,4{9 BENZO-DIAZEPINE-1,2(3H)-DIONES

Publications (1)

Publication Number Publication Date
GB1365455A true GB1365455A (en) 1974-09-04

Family

ID=26890656

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4627872A Expired GB1365455A (en) 1971-11-02 1972-10-06 Imdazobensodiazepines

Country Status (8)

Country Link
US (1) US3846443A (en)
JP (1) JPS5545557B2 (en)
AU (1) AU474359B2 (en)
BE (1) BE790839A (en)
DE (1) DE2252079A1 (en)
FR (1) FR2158414B1 (en)
GB (1) GB1365455A (en)
NL (1) NL7214469A (en)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ZA755418B (en) * 1974-09-11 1977-06-29 Hoffmann La Roche Diazepine derivatives
US4044142A (en) * 1975-02-03 1977-08-23 Roussel Uclaf 1,2-Dihydro-6-phenyl-1H,4H-imidazobenzodiazepin-1-ones
US4134976A (en) * 1975-02-15 1979-01-16 Roussel Uclaf 1,2-Dihydro-6-phenyl-1H,4H-imidazobenzodiazepin-1-ones
US4185102A (en) * 1975-11-04 1980-01-22 Roussel Uclaf 1,2-Dihydro-6-phenyl-1H,4H-imidazobenzodiazepin-1-ones
DE3151597A1 (en) * 1981-12-28 1983-07-07 Kali-Chemie Pharma Gmbh, 3000 Hannover (1,2) -Anellated 1,4-BENZODIAZEPINE COMPOUNDS AND METHOD FOR THE PRODUCTION THEREOF, AND MEDICINAL PRODUCTS CONTAINING THESE COMPOUNDS
US4545935A (en) * 1983-09-12 1985-10-08 Iowa State University Research Foundation, Inc. Amidoalkylation reactions of anilines
AU2003287384A1 (en) * 2002-10-30 2004-06-07 Pointilliste, Inc. Systems for capture and analysis of biological particles and methods using the systems

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1545214A (en) * 1966-11-23 1968-11-08 Hoffmann La Roche Process for the preparation of benzodiazepine derivatives
ZA713364B (en) * 1970-06-18 1972-01-26 Upjohn Co Prganic compounds and process

Also Published As

Publication number Publication date
DE2252079A1 (en) 1973-05-03
JPS5545557B2 (en) 1980-11-18
BE790839A (en) 1973-04-30
US3846443A (en) 1974-11-05
FR2158414B1 (en) 1977-01-14
AU4763472A (en) 1974-04-26
JPS4856699A (en) 1973-08-09
NL7214469A (en) 1973-05-04
AU474359B2 (en) 1976-07-22
FR2158414A1 (en) 1973-06-15

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Legal Events

Date Code Title Description
PS Patent sealed [section 19, patents act 1949]
PCNP Patent ceased through non-payment of renewal fee