Ethyl isocyanate → HCID 136330921, compound

Participants

Reaction Steps

The title compound was prepared by reacting the compound of example 42 with ethyl isocyanate in the same manner as that of example 35. Yield: 90%. 1H NMR (DMSO-d6) δ: 11.76 (1H, br), 8.46 (1H, br), 7.77 (1H, d), 7.57 (1H, dd), 7.06 (1H, d), 6.01 (1H, t), 4.00 (2H, t), 3.09 (2H, m), 2.56 (2H, q), 2.45 (2H, q), 1.73 (2H, m), 1.19 (3H, t), 1.03 (6H, t), 0.97 (3H, t).

Provenance & Evidence