Water → ethyl 8-bromo-2,2-dimethyl-6-oxo-1,2-dihydro-6H-pyrrolo[3,2,1-ij]quinoline-5-carboxylate

反応式

[CH3:1][C:2]1([CH3:20])[N:12]2[C:13]3[C:8]([C:9](=[O:19])[C:10]([C:14]([O:16][CH2:17][CH3:18])=[O:15])=[CH:11]2)=[CH:7][CH:6]=[CH:5][C:4]=3[CH2:3]1.[Br:21]Br.O>C(O)(=O)C>[Br:21][C:6]1[CH:7]=[C:8]2[C:13]3=[C:4]([CH2:3][C:2]([CH3:1])([CH3:20])[N:12]3[CH:11]=[C:10]([C:14]([O:16][CH2:17][CH3:18])=[O:15])[C:9]2=[O:19])[CH:5]=1

参加物

実験手順

Ethyl 2,2-dimethyl-6-oxo-1,2-dihydro-6H-pyrrolo[3,2,1-ij]quinoline-5-carboxylate (Preparation 12, 1.03 g) is dissolved in acetic acid (10 mL) and bromine (213 μL) is added dropwise. The reaction is stirred an additional 30 min and then poured into water (50 mL). The resulting precipitate is filtered and then washed with ether to give 506 mg (38%) of the title compound as white crystals. Physical characteristics: M.p. 227-228° C.; 1H NMR (DMSO-d6) δ8.76, 7.90, 7.79, 4.23, 3.41, 1.63, 1.29; IR (diffuse reflectance) 1727, 1636, 1612, 1592, 1547, 1505, 1393, 1373, 1327, 1303, 1217, 1171, 1167, 1128, 804 cm−1; HRMS (FAB) 350.0386 (C16H16BrNO3+H).