Abstract: Novel substituted N-(1'-ethyl-2'-oxo-5'-pyrrolidinylmethyl) benzamide comnds and derivatives thereof are disclosed. The compounds have psychotropic properties and may be used in pharmaceutical compositions as behavior modifiers.
Type:
Grant
Filed:
April 14, 1978
Date of Patent:
July 17, 1979
Assignee:
Societe d'Etudes Scientifiques et Industrielles de l'Ile de France
Inventors:
Gerard Bulteau, Jacques Acher, Jean C. Monier
Abstract: The azimido benzamide of this invention and its pharmaceutically acceptable salts have an unusually and unexpectedly high therapeutic index and low toxicity in the treatment of emesis in mammals. Pharmacological testing demonstrated the superior efficacy of the compound of this invention over known, similar compounds.
Type:
Grant
Filed:
March 3, 1975
Date of Patent:
August 2, 1977
Assignee:
Societe d'Etudes Scientifiques et Industrielles de l'Ile-de-France
Inventors:
Gerard Bulteau, Jacques Acher, Claude Collignon, Jean-Claude Monier
Abstract: The benzamides of this invention and their pharmaceutically acceptable salts are particularly effective in the treatment of emesis and ulcers in mammals. Their low level of toxicity is compatible with use in human therapy, without undesirable side effects.
Type:
Grant
Filed:
March 5, 1975
Date of Patent:
June 14, 1977
Assignee:
Societe d'Etudes Scientifiques et Industrielles de l'Ile-de-France
Inventors:
Gerard Bulteau, Jacques Acher, Jean-Claude Monier
Abstract: Hypotension in mammals is effective relieved by the administration of dialkylaminoalkyl ethers of 2-alkoxy-3,5-dihalobenzenes. The compounds are relatively non-toxic in dosages required to alleviate such conditions.
Type:
Grant
Filed:
April 26, 1976
Date of Patent:
November 30, 1976
Assignee:
Societe d'Etudes Scientifiques et Industrielles de l'Ile-de-France
Abstract: Excessive histamine in mammals is effectively relieved by the administration of dialkylaminoalkyl ethers of 2-alkoxy-3,5-dihalobenzenes. The compounds are relatively non-toxic in dosages required to alleviate such condition.
Type:
Grant
Filed:
April 26, 1976
Date of Patent:
November 30, 1976
Assignee:
Societe d'Etudes Scientifiques et Industrielles de l'Ile-de-France
Abstract: Pain in mammals is effectively relieved by the administration of dialkylaminoalkyl ethers of 2-alkoxy-3,5-dihalobenzenes. The compounds are relatively non-toxic in dosages required to alleviate such condition.
Type:
Grant
Filed:
April 26, 1976
Date of Patent:
November 30, 1976
Assignee:
Societe d'Etudes Scientifiques et Industrielles de l'Ile-de-France
Abstract: Convulsions, pain, excessive histamine or hypotension in mammals are effectively relieved by the administration of dialkylaminoalkyl ethers of 2-alkoxy-3,5-dihalobenzenes. The compounds are relatively non-toxic in dosages required to alleviate such conditions.
Type:
Grant
Filed:
May 13, 1975
Date of Patent:
August 31, 1976
Assignee:
Societe d'Etudes Scientifiques et Industrielles de l'Ile-de-France
Abstract: 2,5-Disubstituted benzamides are produced by an efficient, effective and economical method by the utilization of 4-methyl 2-chloro 1-3-2-dioxophosphorinane as a catalyst.
Type:
Grant
Filed:
September 23, 1974
Date of Patent:
August 17, 1976
Assignee:
Societe d'Etudes Scientifiques et Industrielles de l'Ile-de-France
Inventors:
Gerard Bulteau, Jacques Acher, Jean-Claude Monier
Abstract: The heterocyclic benzamides of this invention are particularly effective for the treatment of emesis in mammals. For example, when they are administered to dogs in relatively small dosage, they afford 100% protection against vomiting. They are also non-toxic in dosages for effecting complete control of vomiting.
Type:
Grant
Filed:
March 24, 1975
Date of Patent:
May 25, 1976
Assignee:
Societe d'Etudes Scientifiques et Industrielles de l'Ile-de-France
Abstract: The 3-alkoxy-thianaphthene-2-carboxamides of this invention are effective for the treatment of mammals afflicted with emesis. When administered to dogs in dosages of 250 .mu.g/kg, compounds of this invention give 100% protection against vomiting normally induced by subcutaneous administration of apomorphine. The compounds of this invention also favorably modify behavior disturbances in mammals.
Type:
Grant
Filed:
June 26, 1974
Date of Patent:
May 4, 1976
Assignee:
Societe d'Etudes Scientifiques et Industrielles de l'Ile-de-France