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. 2015 Dec 23;10(12):e0134556. doi: 10.1371/journal.pone.0134556

Fig 1. Synthesis of target compounds.

Fig 1

Reagents; i) 120°C, 3 h.; ii) 40% aqu. HBr, 70°C, 12 h; iii) Dry CH2Cl2, N(CH2CH3)3, 0°C; iv) 3-chlorosulfonylbenzoic acid or 4-chlorosulfonylbenzoic acid, N(CH2CH3)3, THF, 0°C to RT; v) (a) N-methyl morpholine, ethyl chloroformate, THF, 0°C to RT, (b) hydroxylamine HCl, KOH, EtOH, 0°C to RT.