Abstract: The invention provides methods for the administration of compounds capable of prolonging a QTc interval and methods for predicting whether an individual is predisposed to such QTc prolongation.
Type:
Grant
Filed:
September 14, 2017
Date of Patent:
February 18, 2020
Assignee:
VANDA PHARMECEUTICALS, INC.
Inventors:
Curt D. Wolfgang, Mihael H. Polymeropoulos
Abstract: Chiral ruthenium catalysts comprising salen and alkenyl ligands are provided for stereoselective cyclopropanation, and methods of cyclopropanation are provided. The chiral ruthenium catalyst is prepared in situ by combining an alkenyl ligand, a deprotonated chiral salen ligand, and a ruthenium (II) metal. A preferred catalyst is prepared in situ by combining 2,3-dihydro-4-venylbenzofuran, deprotonated 1,2-cyclohexanediamino-N,N?-bis(3,5-di-t-butyl-salicylidene) and RuCl2(p-cymene)]2.
Type:
Application
Filed:
December 12, 2011
Publication date:
January 24, 2013
Applicant:
VANDA PHARMECEUTICALS INC.
Inventors:
David E. Pereira, Wade Aumiller, Raymond Dagger
Abstract: Chiral ruthenium catalysts comprising salen and alkenyl ligands are provided for stereoselective cyclopropanation, and methods of cyclopropanation are provided. The chiral ruthenium catalyst is prepared in situ by combining an alkenyl ligand, a deprotonated chiral salen ligand, and a ruthenium (II) metal. A preferred catalyst is prepared in situ by combining 2,3-dihydro-4-venylbenzofuran, deprotonated 1,2-cyclohexanediamino-N,N?-bis(3,5-di-t-butyl-salicylidene) and RuCl2(p-cymene)]2.
Type:
Application
Filed:
December 12, 2011
Publication date:
June 14, 2012
Applicant:
VANDA PHARMECEUTICALS INC.
Inventors:
David E. Pereira, Wade Aumiller, Raymond Dagger
Abstract: Chiral ruthenium catalysts comprising salen and alkenyl ligands are provided for stereoselective cyclopropanation, and methods of cyclopropanation are provided. The chiral ruthenium catalyst is prepared in situ by combining an alkenyl ligand, a deprotonated chiral salen ligand, and a ruthenium (II) metal. A preferred catalyst is prepared in situ by combining 2,3-dihydro-4-venylbenzofuran, deprotonated 1,2-cyclohexanediamino-N,N?-bis(3,5-di-t-butyl-salicylidene) and RuCl2(p-cymene)]2.
Type:
Application
Filed:
May 20, 2010
Publication date:
September 9, 2010
Applicant:
VANDA PHARMECEUTICALS INC.
Inventors:
David E. Pereira, Wade Aumiller, Raymond Dagger