Atevirdine
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Formula | C21H25N5O2 |
Molar mass | 379.464 g·mol−1 |
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Atevirdine is a non-nucleoside reverse transcriptase inhibitor that has been studied for the treatment of HIV.[1]
Synthesis
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Preparation of the pyridylpiperazine moiety starts by aromatic displacement of chlorine from 2-chloro-3-nitropyridine by piperazine to give 3. The secondary amine is then protected as its BOC derivative by reaction with di-tert-butyl dicarbonate (Boc anhydride) to give 4. The nitro group is then reduced by catalytic hydrogenation. Reductive alkylation with acetaldehyde in the presence of lithium cyanoborohydride gives the corresponding N-ethyl derivative. The protecting group is then removed by reaction with TFA. Reaction of the resulting amine with the imidazolide derivative of 5-methoxy-3-indoleacetic acid produces the amide reverse transcriptase inhibitor, atevirdine.
See also
[edit]References
[edit]- ^ Morse GD, Reichman RC, Fischl MA, Para M, Leedom J, Powderly W, et al. (January 2000). "Concentration-targeted phase I trials of atevirdine mesylate in patients with HIV infection: dosage requirements and pharmacokinetic studies. The ACTG 187 and 199 study teams". Antiviral Research. 45 (1): 47–58. doi:10.1016/S0166-3542(99)00073-X. PMID 10774589.
- ^ Romero M (1994). "Atevirdine Mesylate". Drugs of the Future. 19 (1): 9. doi:10.1358/dof.1994.019.01.235297.
- ^ WO 9109849, Romero DL, Mitchell MA, Thomas RC, Palmer JR, Tarpley WG, Aristoff PA, Smith HW, "Diaromatic substituted anti-AIDS compounds", published 1991-07-11, assigned to Upjohn
- ^ Romero DL, Morge RA, Biles C, Berrios-Pena N, May PD, Palmer JR, et al. (Apr 1994). "Discovery, Synthesis, and Bioactivity of Bis(heteroaryl)piperazines. 1. A Novel Class of Non-Nucleoside HIV-1 Reverse Transcriptase Inhibitors". Journal of Medicinal Chemistry. 37 (7): 999–1014. doi:10.1021/jm00033a018. PMID 7512142.