620534-41-0Relevant articles and documents
Pyridine metallations in the synthesis of triazole based NK-1 antagonists
Jeff Thrasher,Hembre, Erik J.,Gardinier, Kevin M.,Savin, Kenneth A.,Hong, Jian Eric,Jungheim, Louis N.
, p. 543 - 547 (2007/10/03)
Regioselective pyridine metallation chemistry was used to produce N-(3-chloropyridin-4-ylmethyl)-N-methyl-1-(3,5-bis-trifluoromethylbenzyl)-5-phenyl-1H-[1,2,3]triazole-4-carboxamide (9a) and [1-(3,5-bis-trifluoromethyl-benzyl)-5-morpholin-4-yl-1H-[1,2,3]t
TRIAZOLE DERIVATIVES AS TACHYKININ RECEPTOR ANTAGONISTS
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Page/Page column 56, (2010/02/07)
This application relates to a compound of Formula (I) or a pharmaceutically acceptable salt thereof, pharmaceutical compositions thereof, and its use as an inhibitor of the NK-1 subtype of tachykinin receptors, as well as a process for its preparation and intermediates therefor. (I) wherein: D is a C1-C3 alkane-diyl; R1 is phenyl, which is optionally substituted with one to three substitutents indpendently selected from the group consisting of halo, C1-C4 alkyl, C1-C4 alkoxy, cyano, difluoromethyl, trifluoromethyl, and trifluoromethoxy; R4 is a radical selected from the group consisting of: (IA), (IB), (IC), (ID), (IE), (IF), (IG), (IH)