Skip to main content
. 2016 Dec 8;8(1):239–246. doi: 10.1039/c6md00553e

Scheme 1. Synthesis of compounds PBP-NH2, PBP-tam, PBP-C2 to PBP-C12, and PBP-NC6 to PBP-NC16. Reagents and conditions: (a) MsOH, rt, 3 days, 59%; (b) R-I (R = ethyl, n-hexyl, n-octyl, n-decyl, n-dodecyl), K2CO3, MeCN, 60–100 °C, 16–47%; (c) 1,2-dichloroethane, K2CO3, MeCN, 48 h, 19%; (d) R-NH2 (R = n-hexyl, n-octyl, n-decyl, n-dodecyl, n-hexadecyl), MeCN, microwave, 120 °C, 4 h, 20–42%; (e) benzyl (2-bromoethyl)carbamate or 2-chloro-N,N-dimethylethylamine Cs2CO3, NaI, DMF, 100 °C, 21 h, 6%; (f) Pd(OH)2, H2, MeOH, rt, 26 h, 25%.

Scheme 1