Abstract: The invention concerns a new, efficient process for the preparation of enantiomerically pure norepinephrine (also known as noradrenaline), or an addition salt thereof, using a catalytic hydrogenation system under hydrogen donor transfer. The invention also discloses a novel intermediate and the process for the preparation thereof.
Abstract: The invention concerns a new, efficient process for the preparation of enantiomerically pure norepinephrine (also known as noradrenaline), or an addition salt thereof, using a catalytic hydrogenation system under hydrogen donor transfer. The invention also discloses a novel intermediate and the process for the preparation thereof.
Abstract: A new and efficient process to obtain Medetomidine enantiomers, a selective and potent ?2-receptor agonist, is presented. Such process comprises a resolution step and a racemization reaction, to be able to recover the unwanted enantiomer which can be recycled as starting material.
Type:
Grant
Filed:
February 26, 2013
Date of Patent:
November 4, 2014
Assignee:
Edmond Pharma S.r.l.
Inventors:
Matteo Zacche', Fulvio Gerli, Pier Andrea Gatti
Abstract: Disclosed is a new and efficient process for the synthesis with high yields and purity of lurasidone hydrochloride, a medicament which is useful as a psychotropic substance. The process involves the preparation of lurasidone base in a reaction system not containing inorganic salts, followed by conversion of the latter to an addition salt with an organic carboxylic acid, which is finally converted to lurasidone hydrochloride.
Abstract: Disclosed is a new and efficient process for the synthesis with high yields and purity of lurasidone hydrochloride, a medicament which is useful as a psychotropic substance. The process involves the preparation of lurasidone base in a reaction system not containing inorganic salts, followed by conversion of the latter to an addition salt with an organic carboxylic acid, which is finally converted to lurasidone hydrochloride.
Abstract: A new and efficient process to obtain Medetomidine enantiomers, a selective and potent ?2-receptor agonist, is presented. Such process comprises a resolution step and a racemisation reaction, to be able to recover the unwanted enantiomer which can be recycled as starting material.
Type:
Application
Filed:
February 26, 2013
Publication date:
August 29, 2013
Applicant:
Edmond Pharma s.r.l.
Inventors:
Matteo Zacche', Fulvio Gerli, Pier Andrea Gatti
Abstract: The present invention provides novel crystalline polymorphs of enantiopure Erdosteine, referred to as Form I and Form II, and processes for the preparation thereof.
Type:
Grant
Filed:
November 10, 2008
Date of Patent:
September 18, 2012
Assignee:
Edmond Pharma S.R.L
Inventors:
Pier Andrea Gatti, Matteo Zacche′, Massimo Nicola
Abstract: The present invention provides novel crystalline polymorphs of enantiopure Erdosteine, referred to as Form I and Form II, and processes for the preparation thereof.
Type:
Application
Filed:
November 10, 2008
Publication date:
September 30, 2010
Applicant:
Edmond Pharma S.R.L
Inventors:
Pier Andrea Gatti, Matteo Zacche', Massimo Nicola
Abstract: Inclusion complexes of dipyridamole with beta cyclodextrins in the molar ratio of dipyridamole to cyclodextrin ranging from 1:1 to 1:12 provides higher and more consistent blood concentrations than can be achieved by the dipyridamole alone.
Abstract: Acetylsalicylic acid thioesters having antipyretic activity and useful for the symptomatic treatment of influenza of formula: ##STR1## wherein n is zero or 1, R.sub.1 is hydrogen, methyl or carboxy and R.sub.2 is hydrogen or an acetamido group; a process for their preparation by reacting a functional derivative of acetylsalicylic acid with the suitable thiol; and pharmaceutical compositions containing them as active ingredient.
Abstract: The compound having formula (I) ##STR1## is obtained by reacting 1,2-diphenyl-4-[2-phenylsulfinyl)-ethyl]-4-hydroxymethyl-pyrazolidine-3,5- dione (hydroxymethylsulfinpyrazone) with nicotinic acid, in the presence of activating agents such as DCCD.(I) is endowed with marked vasodilating, antiaggregating and hypocholesterolemic properties.