Hydrochloric Acid → 2-Phenyl-1-(phenylsulfonyl)-4-(1-piperazinyl)-1H-indole Hydrochloride

참여 물질

반응 단계

tert-Butyl 4-[2-phenyl-1-(phenylsulfonyl)-1H-indol-4-yl]-1-piperazinecarboxylate (30 mg, 0.058 mmol) was dissolved in CH2Cl2 (1 mL) followed by addition of HCl in ether (1 mL). The reaction was shaken for 2 h at room temperature. The resulting precipitate was filtered off and washed with ether giving 20 mg of the desired compound (80%). 1H NMR (270 MHz, DMSO-d6) δ 9.02 (br, 1 H), 7.90–7.80 (m, 3 H), 7.75–7.55 (m, 3 H), 7.32 (s, 1 H), 7.22 (t, J=8 Hz, 1 H), 6.79 (d, J=8 Hz, 1 H), 3.35–310 (m, 8 H). MS (ESI+) for m/z 418 (M+H)+.

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