Synthesis of 5-[(4-phenylpiperazin-1-yl)methyl]pyrrolo-[2,3-d]pyrimidine derivatives as potential dopamine D4 receptor ligands
✍ Scribed by Sabine Linz; Reinhard Troschütz
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2007
- Tongue
- English
- Weight
- 426 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
Abstract
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A series of pyrrolo[2,3‐d]pyrimidine Mannich bases of type 9, 12, 15 and 16 have been prepared as potential dopamine D4 receptor ligands. The syntheses start from 4‐aminopyrimidin‐6‐one 3 with pyrrole annulations and Mannich reactions with formaldehyde and phenylpiperazines 8 as new amine components.
📜 SIMILAR VOLUMES
## Abstract Possible approaches to synthesis of 5‐methyl‐4‐oxo‐2‐(coumarin‐3‐yl)‐__N__‐aryl‐3,4‐dihydrothieno[2,3‐__d__]pyrimidine‐6‐carboxamides **4** have been discussed. It is shown that the preferable approach is cyclization of 2‐iminocoumarin‐3‐carboxamides **1**, utilizing 5‐amino‐3‐methyl‐__
## Abstract For Abstract see ChemInform Abstract in Full Text.