David Scott Coffey - Indianapolis IN, US James Allen Monn - Indianapolis IN, US Concepcion Pedregal-Tercero - Madrid, ES Steven Wayne Pedersen - Indianapolis IN, US
Assignee:
Eli Lilly and Company - Indianapolis IN
International Classification:
A61K 31/16 C07C 233/23
US Classification:
514619, 564193
Abstract:
This invention relates to synthetic excitatory amino acid prodrugs according to formula (I) and processes for their preparation. The invention further relates to methods of using, and pharmaceutical compositions comprising, the compounds for the treatment of neurological disorders and psychiatric disorders.
Crystalline Forms Of {2-[1-(3,5-Bis-Trifluoromethyl-Benzyl)-5-Pyridin-4-Yl-1H-[1,2,3]Triazol-4-Yl]-Pyridin-3-Yl}-(2-Chlorophenyl)-Methanone
Alfio Borghese - Rue Granbonpre', BE David Scott Coffey - Indianapolis IN, US Pamela Kaye Footman - Indianapolis IN, US Steven Wayne Pedersen - Indianapolis IN, US Susan Marie Reutzel-Edens - Zionsville IN, US Shella Lenyonga Tameze - Indianapolis IN, US Carsten Timpe - Hamburg, DE Carsten Weber - Hamburg, DE
Assignee:
Eli Lilly and Company - Indianapolis IN
International Classification:
C07D 401/14 A61K 31/535
US Classification:
546256, 514333
Abstract:
The present invention provides novel crystalline forms of {2-[1-(3,5-bistrifluoromethylbenzyl)-5-pyridin-4-yl-1H-[1,2,3]triazol-4-yl]-pyridin-3-yl}-(2-chlorophenyl)-methanone, compositions thereof, intermediates thereof, methods of using the same, processes for making the same, and processes for making intermediates thereof.
David Scott Coffey - Indianapolis IN, US James Allen Monn - Indianapolis IN, US Concepcion Pedregal-Tercero - Madrid, ES Steven Wayne Pedersen - Indianapolis IN, US
Assignee:
Eli Lilly and Company - Indianapolis IN
International Classification:
A61K 31/16 C07C 233/23
US Classification:
514619, 564193
Abstract:
This invention relates to synthetic excitatory amino acid prodrugs and processes for their preparation. The invention further relates to methods of using, and pharmaceutical compositions comprising, the compounds for the treatment of neurological disorders and psychiatric disorders.
Alexander Godfrey - Greenwood IN, US Steven Pedersen - Indianapolis IN, US
International Classification:
C07D211/44
US Classification:
546/217000
Abstract:
The present invention provides a process for preparing N-protected-4-substituted piperidines of formula (I) wherein Pg represents a suitable nitrogen protecting group; X represents a heterocycle, substituted heterocycle, substituted alkenyl or substituted aryl wherein the substituted heterocycle, substituted alkenyl or substituted aryl are substituted with from 1 to 3 suitable activating groups; and R, R, R, R, R, R, R, and Reach independently represent an alkyl, alkenyl, cycloalkyl, aryl, substituted aryl, heterocycle, or substituted heterocycle, comprising treating a compound of formula (II) wherein the substituents are defined as above, with triethylsilane and trifluoroacetic acid.
Xinchao Chen - Schenectady NY, US Scott Alan Frank - Indianapolis IN, US David Michael Remick - Fishers IN, US Steven Wayne Pedersen - Indianapolis IN, US
Assignee:
ELI LILLY AND COMPANY - Indianapolis IN
International Classification:
A61K 31/55 C07D 403/12 A61P 9/10
US Classification:
51421301, 540593
Abstract:
Compounds of a formulaentitled, trans-4-[[(5S)-5-[[[3,5-bis(trifluoromethyl)phenyl]methyl](2-methyl-2H-tetrazol-5-yl)amino]-2,3,4,5-tetrahydro-7,9-dimethyl-1H-1-benzazepin--yl]methyl]-cyclohexanecarboxylic acid, as a free acid or a pharmaceutically acceptable salt thereof; and hydrates and other solvates in crystalline form; pharmaceutical formulations; and methods of use are disclosed.
Xinchao Chen - Schenectady NY, US Scott Alan Frank - Indianapolis IN, US Steven Wayne Pedersen - Indianapolis IN, US David Michael Remick - Fishers IN, US
Assignee:
ELI LILLY AND COMPANY - Indianapolis IN
International Classification:
A61K 31/55 A61P 9/10 C07D 403/12
US Classification:
51421301, 540593
Abstract:
Abstract Compounds of a formula entitled, trans-4-[[(5S)-5-[[[3,5-bis(trifluoromethyl)phenyl]methyl](2-methyl-2H-tetrazol-5-yl)amino]-2,3,4,5-tetrahydro-7,9-dimethyl-1H-1-benzazepin-1-yl]methyl]-cyclohexanecarboxylic acid, as a free acid or a pharmaceutically acceptable salt thereof, hydrate, and hydrate in crystalline form; pharmaceutical formulations; and methods of use are disclosed.
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