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. Author manuscript; available in PMC: 2017 Jul 11.
Published in final edited form as: J Med Chem. 2017 Mar 13;60(6):2305–2325. doi: 10.1021/acs.jmedchem.6b01568

Scheme 3.

Scheme 3

Syntheses of compound 8p and 8qa

aReagents and conditions (a) MeNH(OMe)•HCl, EDCI, Et3N, CH2Cl2, 41% (b) BnMgCl, THF, 0 °C to RT, 25%. (c) IBCF, NMM, THF, 0 °C, then aq. NaBH4, 0 °C, 41%. (d) MsCl, Et3N, THF, 0 °C. (e) aniline, Et3N, THF, 20% (2 steps).