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. Author manuscript; available in PMC: 2021 May 28.
Published in final edited form as: J Med Chem. 2020 May 6;63(10):5501–5525. doi: 10.1021/acs.jmedchem.0c00442

Scheme 1.

Scheme 1.

Synthesis of 3, 6a-6c, 10a and 10b.

Reagents and conditions: (a) Ethanol, NaOH, reflux, 47%; (b) NaBH3CN, CH3COOH, methanol, 70–80% yield; (c) Boc2O, TEA, DCM, 80–85% yield; (d) Propionaldehyde or benzaldehyde, NaBH3CN, HCl, Ethanol, 60–70%.