4-Tert-Butylaniline → HCID 11705436, compound

Participants

Reaction Steps

The title product was prepared using the procedure as described in Example 1C, substituting the product of Example 24A for the product of Example 1B, and substituting 4-trifluoromethanesulfonyl-phenylamine for 4-tert-butylaniline. 1H NMR (300 MHz, DMSO-d6) δ 7.63 (t, J=4.9 Hz, 1H), 8.29 (m, 2H), 8.39 (m, 2H), 8.70 (d, J=8.1 Hz, 1H), 8.86 (s, 1H), 8.95 (dd, J=8.1, 1.4 Hz, 1H), 9.05 (d, J=5.1 Hz, 2H), 11.46 (s, 1H).

Provenance & Evidence