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Published on: June 23, 2019
Novel tetrahydropyrido[3,2-c]pyrroles as 5-HT(7) antagonists
Dale A Rudolph1, Curt A Dvorak, Lisa Dvorak
1Johnson & Johnson Pharmaceutical Research and Development, LLC, 3210 Merryfield Row, San Diego, CA 92121, United States. drudolph@its.jnj.com
Abstract:
The synthesis and SAR for a novel series of tetrahydropyrido[3,2-c]pyrroles is described. Optimization of the pendant aryl ring lead to high binding affinity at the 5-HT(7) receptor when small lipophilic groups were placed in the para position. Modification of the N-benzyl group and secondary amine were not well tolerated. A representative set of compounds was shown to be functional antagonists of the 5-HT(7) receptor.
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