An Expeditious Synthesis of 4(5) [3-Aminopropyl] Imidazole
- 1 February 1987
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 17 (2) , 223-227
- https://doi.org/10.1080/00397918708057225
Abstract
Inpmmidine 1is a highly potent and selective agonist for histamine receptors.1 The synthesis of inpmnidine and structure activity considerations have recently been described. Inpmmidine also has potential valus for the tEatrnent of catecholamine-insensitive congestive heart failure.3 It has been noted,3 however, that the synthesis of inpromidine is too canplicated and very expensive. One reason for this is the difficulty associated with the synthesis of the crucial inter mxiiate 4(5) [3-aminopmpyl] imidazole 2hereafter referred to as imi damlylpmpylamine.Keywords
This publication has 5 references indexed in Scilit:
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- Possible value of H2-receptor agonists for treatment of catecholamine-insensitive congestive heart failurePharmacology & Therapeutics, 1984
- Impromidine (SK&F 92676) is a very potent and specific agonist for histamine H2 receptorsNature, 1978
- Attempted inhibition of histidine decarboxylase with .beta.-alkyl analogs of histidineJournal of Medicinal Chemistry, 1977
- Amine hydrochlorides by reduction in the presence of chloroformThe Journal of Organic Chemistry, 1972