1-Methylpiperazine → HCID 2974347, compound

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Reaction Steps

N-ethyl-5-(4-methyl-1-piperazinyl)-2-nitroaniline was prepared from 2,4-difluoro-1-nitrobenzene and methylpiperazine using the same method described for N-ethyl-2-nitro-5-(1-piperazinyl)aniline and was obtained as yellow solid (99%). 1H NMR (CDCl3) δ 8.30 (br s, 1H), 8.08–8.04 (m, 1H), 6.25–6.20 (m, 1H), 5.89–5.86 (m, 1H), 3.45–3.39 (m, 4H), 3.35–3.25 (m, 2H), 2.56–2.50 (m, 4H), 2.35 (s, 3H), 1.37 (tr, J=7.2 Hz, 3)); 13C NMR δ(CDCl3) 155.92, 147.72, 128.99, 124.19, 104.30, 94.37, 54.78, 47.05, 46.25, 37.73, 14.43; MS (posESI) m/z=found 264.1575, calc 264.1586. Anal. (C13H20N4O2,0.5 H2O) C, H, O.

Provenance & Evidence