HCID 11691173, compound → HCID 55283965, compound

Participants

Reaction Steps

N-(tert-butoxycarbonyl)-N,O-dimethyl-L-homoserine was converted to the corresponding amide, followed by removal of the nitrogen protecting group using an analogous as process to that described in Example 7 for the preparation of N2,O-dimethyl-L-serinamide, to give N2,O-dimethyl-L-homoserinamide; 1H NMR spectrum: (DMSO d6) 1.58 (m, 1H), 1.69 (m, 1H), 1.80 (brs, 1H), 2.17 (s, 3H), 2.84 (dd, 1H), 3.20 (s, 3H), 3.34 (m, 2H), 6.93 (brs, 1H), 7.27 (brs, 1H).

Provenance & Evidence