反应详情

6-Chloro-2-(1-naphthylamino)-2,3,4,9-tetrahydro-1H-pyrrolo[3,4-b]quinoline-1,3,9-trione (1.30 g, 3.34 mM) was stirred in methanol (0.65 L) and methanesulfonic acid (65 mL) was added. The brown suspension was heated toreflux for 16 hours during which the solids dissolved to give a brown solution. This solution was cooled to room temperature. Addition of ice (10 mL) gave a tan suspension which was stirred for 1.5 hours. The suspension was filtered (the filtrate was saved for use in Example 24) andthe collected solids were washed with methanol and ether to give the title compound (0.560 g, 43%) as a dull yellow powder, mp 374°-376° C.; MS(CI): 390 (M+H). Analysis for 21H12ClN3O3·0.20 H2O: Calculated: C, 64.10; H, 3.18; N, 10.68 Found: C, 63.91; H, 3.42; N, 10.61 1H NMR 13.40 (s, 1H exchangeable), 12.58 (s, 1H exchangeable), 8.35 (d, J=8.70 Hz, 1H), 8.25 (d, J=1.76 Hz, 1H), 8.12-8.07 (m, 2H), 7.74-7.53 (m, 6H).

1. temperatureThe brown suspension was heated toreflux for 16 hours during which the solids
2. dissolutiondissolved
3. customto give a brown solution
4. customgave a tan suspension which
5. filtrationThe suspension was filtered (the filtrate
6. washwere washed with methanol and ether