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. Author manuscript; available in PMC: 2022 May 24.
Published in final edited form as: Bioorg Med Chem. 2021 Sep 17;48:116414. doi: 10.1016/j.bmc.2021.116414

Scheme 2.

Scheme 2.

The synthetic route of phenylalanine derivatives (series I-IV). Reagents and Conditions: (i) methyl 3-chlorosulfonylbenzoate or methyl 2-(chlorosulfonyl) acetate or methyl chlorooxoacetate or 3-nitrobenzoyl chloride or amine fragments, TEA, CH2Cl2, 0°C, 4 h; (ii) NaOH, THF/H2O (V:V = 1:1), r.t., 2 h; (iii) amine fragments, HATU, DIEA, CH2Cl2, r.t., 8 h; (iv) SnCl2·2H2O, EtOH, N2, r.t., 8 h.(v) sulfonyl chloride substituents, TEA, CH2Cl2, 0 °C, 4 h.