[ClH:1].[O:2]=[C:3]([N:6]1[CH2:10]CC[CH2:7]1)[CH2:4][NH2:5].Cl.CNC.CN1CCO[CH2:18][CH2:17]1>>[ClH:1].[NH2:5][C@@H:4]([CH2:17][CH3:18])[C:3]([N:6]([CH3:7])[CH3:10])=[O:2](2S)-2-Amino-N,N-dimethylbutanamide, hydrochloride salt was prepared in a manner similar to 2-oxo-2-(1-pyrrolidinyl)ethanamine, hydrochloride salt (Example 69), utilizing N-CBZ-L-2-aminobutyric acid in place of N-CBZ-glycine, utilizing dimethylamine, hydrochloride salt in place of pyrrolidine, and using 3 equivalents of NMM in Part A. (M+H)+: 130.9.
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