We present the results of our study on the ultrafast solvent dynamics of the amides formamide (FA), N,N-dimethylformamide (DMF), and their deuterated analogs HCOND2 (d(2)-FA) and DCON(CD3)(2) (d(7)-DMF) using femtosecond optical-heterodyne-detected Raman-induced Kerr effect spectroscopy (OHD-RIKES). Using nearly transform-limited 50 fs optical pulses and the Fourier-transform relationship, we have studied the liquid dynamics in the frequency range from 0.6 to 400 cm(-1). In comparison to the depolarized Rayleigh spectroscopy technique, OHD-RIKES is shown to provide more accurate and detailed information about the low-frequency region that includes the rotational reorientation, librational, and collision-induced dynamics. The effect of deuterium isotope substitution on the inertial as well as diffusive reorientational dynamics of these amide liquids is discussed.