HCID 71060717, compound → HCID 71062483, compound

Participants

Reaction Steps

Following a procedure analogous to that for the synthesis of Intermediate 223E, (E)-ethyl 2-(2-(4-(3-chlorophenoxy)phenyl)hydrazono)acetate (60 mg, 0.19 mmol) and tert-butyl 4-(2-nitrohex-1-enyl)-3-(1,2,3,4-tetrahydroisoquinoline-2-carbonyl)benzoate (88 mg, 0.19 mmol) were converted to the title compound (62 mg, 45%) as a pale yellow oil. 1H NMR (CDCl3, 1:1 mixture of amide rotamers) δ 8.10 (dd, J=8, 2 Hz, 1H), 8.05-8.04 (m, 1H), 7.44-6.83 (m, 13H), 5.02-4.98 (m, 1H), 4.48-4.38 (m, 1H), 4.33-4.28 (m, 2H), 4.18-3.98 (m, 1H), 3.58-3.32 (m, 1H), 2.85-2.50 (m, 4H), 1.61 (s, 9H), 1.29 (t, J=8 Hz, 1.5H), 1.19 (t, J=8 Hz, 1.5H), 1.15-0.81 (m, 4H), 0.65-0.61 (m, 3H); MS(ESI+) m/z 734.3 (M+H)+.

Provenance & Evidence