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. 2019 Jan 10;10(2):315–325. doi: 10.1039/c8md00545a

Scheme 1. Synthesis of aminoalcohol 7a. Reagents and reaction conditions: (a) 1. CDI, CH2Cl2, rt, 45 min; 2. CH3NHOCH3, CH2Cl2, rt, 24 h, 89%. (b) DIBAL-H, toluene, –78 °C, 2 h. (c) (C6H5)3P Created by potrace 1.16, written by Peter Selinger 2001-2019 CHCO2Et, CH2Cl2, rt, 24 h, 80%. (d) Benzylamine, EtOH, 80 °C, 20 h, 42%. (e) TosCl, DIPEA, CH2Cl2, rt, 24 h, 87%. (f) 0.1 M NaOH, THF/H2O, rt, 26 h, 69%. (g) P4O10, CH2Cl2, –10 °C, 23 h, 27%. (h) NaBH4, MeOH, 0 °C to rt, 5.5 h, 78%. (i) Mg0, MeOH, rt, ultra-sonic, 5 h, 64%.

Scheme 1