Thiomorpholine → HCID 11688373, compound

Participants

Reaction Steps

The title compound was prepared from commercially available ethyl isonipecotate, 3-fluoro-4-methylbromobenzene as the aryl halide, and thiomorpholine as the secondary amine utilizing general procedures A and B described above. 1H NMR (300 MHz, CDCl3) 1H NMR (CDCl3) δ 7.02 (dd, J=7.2, 9.2 Hz, 1H), 6.63-6.55 (m, 2H), 3.90 (m, 2H), 3.80 (m, 2H), 3.70 (m, 1H), 3.65 (m, 1H), 2.75-2.51 (m, 7H), 2.17 (d, J=1.6 Hz, 3H), 2.01 (dd, J=3.3, 13.4 Hz, 1H), 1.91 (dd, J=4.0, 11.4 Hz, 1H), 1.80 (m, 1H), 1.76 (m, 1H). ESI MS: 323.3 (MH+).

Provenance & Evidence