Abstract: An improved catalyst is disclosed for a process involving the preparation of benzylidene intermediates useful in the preparation of 1,4-dihydropyridine compounds and derivatives thereof useful as medicines such as for example felodipine. This is accomplished by the condensation of an aldehyde and an acetoacetate in the presence of a novel catalyst system that includes a pyridyl carboxylic acid and a secondary amine. It has been found that through the use of the present invention the purity and yield of the desired isomer of the benzylidene intermediate can be maximized, thus avoiding the requirement of additional purification steps. The use of these intermediates can then be further reacted to form the required dihydropyridines, again having a very high purity and yield compared with the prior art.
Type:
Grant
Filed:
April 8, 2004
Date of Patent:
February 22, 2005
Assignee:
Apotex Pharmachem Inc.
Inventors:
Daqing Che, Bhaskar Reddy Guntoori, K. S. Keshava Murthy
Abstract: The present invention relates to a peritoneal dialysis solution comprising at least one amino sugar in an effective amount sufficient to create an osmotic pressure to effect the removal of water by diffusion from the patient's blood across the peritoneal membrane into the solution. In one embodiment the at least one amino sugar is selected from the group consisting of acetylated amino sugars, preferably N-acetylglucosamine, deacetylated amino sugars and combinations thereof.
Abstract: A portable device for dispensing drywall patching compound (mud) onto drywall is disclosed. The dispenser has a device on one end used for metering the drywall compound in a controlled manner and has affixed to at least one side an abrasive surface, preferably sand paper that can be used to smooth out the drywall compound when dry. As a preferred embodiment, the cap of the container contains a spatula or other device that can be used to shape the compound as it is being applied.
Abstract: The present invention relates to a process for the production of (S)-1,2,3,4-tetrahydro-6,7-dialkoxy-3-isoquinolinecarboxylic acid compounds (1) and their derivatives from Levodopa (L-Dopa). The ultimately prepared compounds are used as intermediates for, but not limited to, the preparation of substituted derivatives of 1,2,3,4-tetrahydro-6,7-dialkoxy-3-isoquinolinecarboxylic acid
wherein
R1 is hydrogen, lower alkyl, C2-C12 acyl, or R1O together are methylenedioxy;
R2 is hydrogen, alkyl, substituted alkyl, alkenyl, substituted alkenyl, aryl, substituted aryl, aralkyl or substituted aralkyl group; and
R3 is hydrogen, C2-C12 acyl group, benzyl, alkoxylcarbonyl group, or aralkoxyl carbonyl group.
Abstract: A process for the preparation of Nefazodone hydrochloride comprising direct conversion of semicarbazide dihydrochloride 3 into Nefazodone hydrochloride which process involves a reaction of triethyl orthopropionate in the presence of trimethylsilylchloride and hydrochloric acid.
Type:
Grant
Filed:
September 17, 2001
Date of Patent:
July 22, 2003
Assignee:
Brantford Chemicals Inc.
Inventors:
K. S. Keshava Murthy, Bhaskar Reddy Guntoori, Daqing Che
Abstract: This invention relates to the preparation of 3-sulfonamido-4-arylaminopyridines by heating a 3-sulfonamido-4-aminopyridine with an aryl halide in the presence of an alkaline compound, a copper-containing agent and in the presence of a polar protic solvent.
Type:
Grant
Filed:
November 14, 2002
Date of Patent:
July 15, 2003
Assignee:
Brantford Chemicals Inc.
Inventors:
Carlos B. Zetina-Rocha, Bhaskar Reddy Guntoori, Stephen E. Horne
Abstract: A process for the manufacture of 3,5-diamino-6-substituted-1,2,4-triazines is disclosed which comprises the steps of:
(a) reacting a compound of formula (II):
with aminoguanidine salts,
(b) dehydrating the compound obtained to form a compound of formula IV,
and
(c) cyclization of the compound of formula IV into a 3,5-diamino-6-substituted-1,2,4-triazine compound of formula I or into a hydrated form thereof.
Type:
Grant
Filed:
January 16, 2002
Date of Patent:
July 1, 2003
Assignee:
Brantford Chemicals Inc.
Inventors:
Bhaskar Reddy Guntoori, Daqing Che, K. S. Keshava Murthy
Abstract: A pharmaceutical composition for controlled onset and sustained release of an active ingredient, said composition comprising:
(i) a core comprising:
(a) an active ingredient;
(b) a hydrophilic carrier;
(c) a hydrodynamic diffusion enhancer; and optionally
(d) conventional pharmaceutically acceptable excipients selected from the group consisting of binders, fillers and lubricants and combinations thereof; and
(ii) a functional coating membrane surrounding said core.
Abstract: A pit form comprising two substantially parallel side members having two ends and a substituting perpendicular rear member extending between proximate the same ends of the side members in use, each of the side members and the rear member having compatible male and female engaging portions to interconnect said members to form said pit form.