Synthesis of Novel IP Agonists via N-Aminoethyl Cyclic Amines Prepared by Decarboxylative Ring-Opening Reactions
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ID: 273467
2012
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Abstract
An efficient synthesis of a highly potent and selective IP (PGI2 receptor) agonist that is not structurally analogous to PGI2 is described. This synthesis is accomplished through the following key steps: Nucleophilic ring-opening of 3-(4-chlorophenyl)-oxazolidin-2-one prepared by a one-pot procedure with 4-piperidinol and selective O-alkylation of 1-(2-(4-chlorophenylamino)ethyl)piperidin-4-ol. The obtained compound is a potent and selective IP agonist displaying a long duration of action.
| Reference Key |
iseki2012moleculessynthesis
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| Authors | Yasuhiro Morita,Takeshi Ishigaki,Kuniaki Kawamura,Ryoji Hayashi,Masafumi Isogaya,Mika Kitsukawa,Mitsuko Miyamoto,Masashi Uchida,Katsuhiko Iseki;Yasuhiro Morita;Takeshi Ishigaki;Kuniaki Kawamura;Ryoji Hayashi;Masafumi Isogaya;Mika Kitsukawa;Mitsuko Miyamoto;Masashi Uchida;Katsuhiko Iseki; |
| Journal | molecules |
| Year | 2012 |
| DOI |
10.3390/molecules17021233
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| URL | |
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