Jump to content

Atevirdine

From Wikipedia, the free encyclopedia
(Redirected from Ateviridine)

Atevirdine
Identifiers
  • [4-[3-(ethylamino)pyridin-2-yl]piperazin-1-yl]-(5-methoxy-1H-indol-2-yl)methanone
CAS Number
PubChem CID
DrugBank
ChemSpider
UNII
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC21H25N5O2
Molar mass379.464 g·mol−1
3D model (JSmol)
  • CCNC1=C(N=CC=C1)N2CCN(CC2)C(=O)C3=CC4=C(N3)C=CC(=C4)OC
  • InChI=InChI=1S/C21H25N5O2/c1-3-22-18-5-4-8-23-20(18)25-9-11-26(12-10-25)21(27)19-14-15-13-16(28-2)6-7-17(15)24-19/h4-8,13-14,22,24H,3,9-12H2,1-2H3
  • Key:UCPOMLWZWRTIAA-UHFFFAOYSA-N

Atevirdine is a non-nucleoside reverse transcriptase inhibitor that has been studied for the treatment of HIV.[1]

Synthesis

[edit]
Atevirdine synthesis:[2][3] SAR:[4]

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]
  1. ^ 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.
  2. ^ Romero M (1994). "Atevirdine Mesylate". Drugs of the Future. 19 (1): 9. doi:10.1358/dof.1994.019.01.235297.
  3. ^ 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 
  4. ^ 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.