2-(4-(4-(2-Methoxyphenyl)piperazin-1-yl)-3-hydroxybutyl)isoindoline-1,3-dione → 4-Amino-1-(4-(2-methoxy-phenyl)-piperazin-1-yl)-butan-2-ol

Participants

Reaction Steps

Prepared from 26b in a similar fashion as described above for 27a. Yield: 69%. Wax. 1H NMR (CDCl3): δ 1.59 (m, 2H), 2.41 (m, 2H), 2.57 (m, 2H), 2.79-2.81 (m, 9H), 3.86 (s, 3H), 3.91 (m, 1H), 6.86 (d, J 7.5, 1H), 6.91-6.96 (m, 2H), 6.98-7.03 (m, 1H). 13C NMR (CDCl3): δ 37.3, 39.7, 50.9, 53.6, 55.5, 64.5, 66.2, 111.2, 118.3, 121.1, 123.1, 141.3, 152.3.

Provenance & Evidence