Sistesis Senyawa Antimalaria 3-(2-Hidrosietil)-2-Metil-1,10-Fenantrolin-4-OL dari 8-Aminoquinolin = Synthesis of Antimalarial 3-(2-Hydroxyethyl)-2-methyl-1,10-phenanthroline-4-ol from 8-Aminoquinoline
Main Author: | Perpustakaan UGM, i-lib |
---|---|
Format: | Article NonPeerReviewed |
Terbitan: |
[Yogyakarta] : Universitas Gadjah Mada
, 2005
|
Subjects: | |
Online Access: |
https://repository.ugm.ac.id/17477/ http://i-lib.ugm.ac.id/jurnal/download.php?dataId=235 |
Daftar Isi:
- It has been conducted the synthesis of 3-(2-hydroxyethyl)-2- methyl-1,10-phenanthroline-4-ol was carried out from 8-aminoquinoline which are expected to posses antimalarial activity. The experiment perfomed consisted of two steps i.e (1) reaction of 8-aminoquinoline with 2-acetyl-butyrolactone and (2) cyclization of the resulted 341-(quinolin-8-ylamino)- ethylidene]-4,5-dihydro-furan-2-one. Identification of the products were carried out by means of infra red (IR) spectroscopy, proton nuclear magnetic resonance (1H-NMR) spectroscopy, and mass spectroscopy (MS). The reaction of 8-aminoquinoline with 2-acetyl-butyrolactone was performed in toluene at reflux for 6 hours in the presence of p-toluensulfonic acid as catalyst. This reaction gave 3- [1-(quinolin-8-ylamino)-etiliden]-4,5-dihidro-furan-2-on in 60.6% yield. The cyclization of 341-(quinoline-8-ylamino)-ethyliden]-4,5- dihydro-furan-2-one was conducted in cloroform at reflux for 4 hours in the preserice of H2SO4 as catalyst and also tween 80 as transfer phase catalyst to give 3-(2-hydroxy-ethyl)-2-methyl-1,10- phenanthroline-4-ol in 76.2% yield. Key words : antimalarial, 8-aminoquinoline, cyclization, 1,10- phenantroline.