Perbandingan Metode Sintesis Senyawa 1-benzil-3-(4-etil-benzoil)urea dan 1-benzil-3-(4-klorometil-benzoil)urea sebagai Calon Obat Antikanker

Suhud, Farida and Tjahjono, Daryono Hadi and Yuniarta, Tegar Achsendo and Putra, Galih Satrio and Sulistyowaty, Melanny Ika (2021) Perbandingan Metode Sintesis Senyawa 1-benzil-3-(4-etil-benzoil)urea dan 1-benzil-3-(4-klorometil-benzoil)urea sebagai Calon Obat Antikanker. Jurnal Farmasi Dan Ilmu Kefarmasian Indonesia, 8 (3). pp. 277-283. ISSN 2406-9388; E-ISSN: 2580-8303

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Tegar Achsendo Yuniarta_Perbandingan Metode Sintesis Senyawa 1-benzil-3-(4-etil-benzoil)urea dan 1-benzil-3-(4-klorometil-benzoil)urea sebagai Calon Obat Antikanker.pdf

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Official URL / DOI: https://e-journal.unair.ac.id/JFIKI/article/view/2...

Abstract

Background: The research of anticancer drugs is still being developed, especially on the hydroxyurea group. Objective: This study aimed to compare the synthesis methods of 1-benzyl-3-benzoylurea derivatives, namely 1-benzyl-3-(4-ethyl-benzoyl)urea and 1-benzyl-3-(4-chloromethyl-benzoyl)urea. Methods: Optimization of the synthesis method was carried out by comparing the synthesized products with and without reflux heating. The products obtained were subjected to structure elucidation analysis by using FTIR, 1H-NMR, and 13C-NMR. Results: The reflux synthesis method produced by-product compounds, which needed to be separated by column chromatography. The method without heating is preferred because it did not produce by-product compounds. Conclusion: The method of synthesizing 1-benzyl-3-benzoylurea derivatives was recommended without using reflux heating, and in the future, researchers must find a better approach to get a better yield.

Item Type: Article
Uncontrolled Keywords: 1-benzyl-3-benzoylurea derivatives, synthesis, method comparison, reflux
Subjects: Q Science > QD Chemistry
Divisions: Faculty of Pharmacy > Department of Pharmacy
Depositing User: TEGAR ACHSENDO YUNIARTA
Date Deposited: 30 Apr 2022 00:21
Last Modified: 21 Jun 2022 07:38
URI: http://repository.ubaya.ac.id/id/eprint/41754

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