GB1177957A - Production of Oxazepines and Thiazepines - Google Patents

Production of Oxazepines and Thiazepines

Info

Publication number
GB1177957A
GB1177957A GB4366769A GB4366769A GB1177957A GB 1177957 A GB1177957 A GB 1177957A GB 4366769 A GB4366769 A GB 4366769A GB 4366769 A GB4366769 A GB 4366769A GB 1177957 A GB1177957 A GB 1177957A
Authority
GB
United Kingdom
Prior art keywords
alkyl
piperazinyl
hydroxy
pyrrolidino
piperidino
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
GB4366769A
Inventor
Charles Frederick Howell
Robert Allis Hardy
Nicanor Quinones Quinones
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.)
Wyeth Holdings LLC
Original Assignee
American Cyanamid 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 American Cyanamid Co filed Critical American Cyanamid Co
Priority to GB4366769A priority Critical patent/GB1177957A/en
Priority to GB5771066A priority patent/GB1177956A/en
Publication of GB1177957A publication Critical patent/GB1177957A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/06Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D267/00Heterocyclic compounds containing rings of more than six members having one nitrogen atom and one oxygen atom as the only ring hetero atoms
    • C07D267/02Seven-membered rings
    • C07D267/08Seven-membered rings having the hetero atoms in positions 1 and 4
    • C07D267/12Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
    • C07D267/16Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems condensed with two six-membered rings
    • C07D267/20[b, f]-condensed
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D281/00Heterocyclic compounds containing rings of more than six members having one nitrogen atom and one sulfur atom as the only ring hetero atoms
    • C07D281/02Seven-membered rings
    • C07D281/04Seven-membered rings having the hetero atoms in positions 1 and 4
    • C07D281/08Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
    • C07D281/12Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems condensed with two six-membered rings
    • C07D281/16[b, f]-condensed
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/02Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Abstract

1,177,957. Tranquilizers. AMERICAN CYANAMID CO. 23 Dec., 1966, No. 43667/69. Divided out of 1,177,956. Heading A5B. [Also in Division C2] Pharmaceutical compositions, having tranquilizing and, in some instances, antidepressant and analgesic properties, comprise a compound of formula I: in which X is oxygen or sulphur, one of R 1 and R 2 is H, C 1-6 alkyl, C 1-6 alkoxy, halogen or trifluoromethyl and the other of R 1 and R 2 is H, C 1-6 alkoxy or halogen, Y is hydroxy, amino, C 1-6 alkylamino, di-(C 1-6 alkyl) amino, 1-piperazinyl, 4-C 1-6 alkyl-1-piperazinyl, 4-hydroxy-C 1-6 alkyl-1-piperazinyl, pyrrolidino, C 1-6 alkyl-pyrrolidino, piperidino, C 1-6 alkyl piperidino, morpholino or C 1-6 alkyl morpholino, R is C 1-6 alkyl, and n is 2, 3 or 4; or the -N(R)- C n H n -Y group taken together represents 1- piperazinyl; 4-C 1-6 alkyl-1-piperazinyl or 4- hydroxy-C 1-6 alkyl-1-piperazinyl, together with a pharmaceutically acceptable diluent or carrier. The compositions may be administered orally, e.g. in the form of tablets, capsules, dragees, drops, emulsions, suspensions and syrups, and in chocolate, candy or chewing gum, or parenterally in the form of aqueous solutions.
GB4366769A 1966-12-23 1966-12-23 Production of Oxazepines and Thiazepines Expired GB1177957A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
GB4366769A GB1177957A (en) 1966-12-23 1966-12-23 Production of Oxazepines and Thiazepines
GB5771066A GB1177956A (en) 1966-12-23 1966-12-23 Production of Oxazepines and Thiazepines

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB4366769A GB1177957A (en) 1966-12-23 1966-12-23 Production of Oxazepines and Thiazepines
GB5771066A GB1177956A (en) 1966-12-23 1966-12-23 Production of Oxazepines and Thiazepines

Publications (1)

Publication Number Publication Date
GB1177957A true GB1177957A (en) 1970-01-14

Family

ID=26265220

Family Applications (2)

Application Number Title Priority Date Filing Date
GB5771066A Expired GB1177956A (en) 1966-12-23 1966-12-23 Production of Oxazepines and Thiazepines
GB4366769A Expired GB1177957A (en) 1966-12-23 1966-12-23 Production of Oxazepines and Thiazepines

Family Applications Before (1)

Application Number Title Priority Date Filing Date
GB5771066A Expired GB1177956A (en) 1966-12-23 1966-12-23 Production of Oxazepines and Thiazepines

Country Status (1)

Country Link
GB (2) GB1177956A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996018622A1 (en) * 1994-12-12 1996-06-20 Allelix Biopharmaceuticals Inc. N-methyl piperazine compounds having dopamine receptor affinity
US7491715B2 (en) 2003-12-22 2009-02-17 Acadia Pharmaceuticals, Inc. Amino substituted diaryl[a,d]cycloheptene analogs as muscarinic agonists and methods of treatment of neuropsychiatric disorders

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996018622A1 (en) * 1994-12-12 1996-06-20 Allelix Biopharmaceuticals Inc. N-methyl piperazine compounds having dopamine receptor affinity
US5700445A (en) * 1994-12-12 1997-12-23 Allelix Biopharmaceuticals, Inc. N-methyl piperazine compounds having dopamine receptor affinity
US5968478A (en) * 1994-12-12 1999-10-19 Allelix Biopharmaceuticals, Inc. N- methyl piperazine compounds having dopamine receptor affinity
US7491715B2 (en) 2003-12-22 2009-02-17 Acadia Pharmaceuticals, Inc. Amino substituted diaryl[a,d]cycloheptene analogs as muscarinic agonists and methods of treatment of neuropsychiatric disorders
US7517871B2 (en) 2003-12-22 2009-04-14 Acadia Pharmaceuticals, Inc. Amino substituted diaryl[a,d]cycloheptene analogs as muscarinic agonists and methods of treatment of neuropsychiatric disorders
US7622461B2 (en) 2003-12-22 2009-11-24 Acadia Pharmaceuticals Inc. Amino substituted diaryl[a,d]cycloheptene analogs as muscarinic agonists and methods of treatment of neuropsychiatric disorders

Also Published As

Publication number Publication date
GB1177956A (en) 1970-01-14

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