HCID 54760086, compound → HCID 54670047, compound
Reaction equation
C[O:2][C:3]1[CH:4]=[C:5]([C:9]2[N:14]=[C:13]3[N:15]([CH2:18][C:19]4[CH:20]=[C:21]5[C:26](=[CH:27][CH:28]=4)[N:25]=[CH:24][CH:23]=[CH:22]5)[N:16]=[N:17][C:12]3=[CH:11][CH:10]=2)[CH:6]=[CH:7][CH:8]=1>ClCCl.B(Br)(Br)Br>[N:25]1[C:26]2[C:21](=[CH:20][C:19]([CH2:18][N:15]3[C:13]4=[N:14][C:9]([C:5]5[CH:4]=[C:3]([OH:2])[CH:8]=[CH:7][CH:6]=5)=[CH:10][CH:11]=[C:12]4[N:17]=[N:16]3)=[CH:28][CH:27]=2)[CH:22]=[CH:23][CH:24]=1Participants
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of example 2 (0.110 g, 0.299 mmol) in dichloromethane (1 ml), BBr3 (1M in dichloromethane, 0.82 ml) was added at 0° C. and the reaction mixture was warmed to RT and stirred for 1 h. The reaction mixture was quenched with 1.5N HCl solution and extracted with dichloromethane. The organic layer was dried over sodium sulphate and concentrated. The crude product was purified by column chromatography with methanol:dichloromethane to afford the title compound as an off-white solid (0.030 g, 28%), M.P.: 255-257° C. 1H-NMR (δ ppm, DMSO-d6, 400 MHz): 9.70 (s, 1H), 8.88 (dd, J=4.1, 2.6 Hz, 1H), 8.62 (d, J=8.7 Hz, 1H), 8.37 (d, J=8.0 Hz, 1H), 8.04 (m, 3H), 7.83 (dd, J=8.7, 1.8 Hz, 1H), 7.64 (s, 1H), 7.64 (d, J=8.6 Hz, 1H), 7.53 (dd, J=8.3, 4.2 Hz, 1H), 7.35 (t, J=7.9 Hz, 1H), 6.92 (dd. J=7.9, 1.4 Hz, 1H), 6.19 (s, 2H). MS (m/z): 354.02 (M+).
Workup
- customThe reaction mixture was quenched with 1.5N HCl solution
- extractionextracted with dichloromethane
- dry with materialThe organic layer was dried over sodium sulphate
- concentrationconcentrated
- customThe crude product was purified by column chromatography with methanol
Sources & evidence
- ORD record
- ord-2507c5e7a1a2498c9e42df3220734e51
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08912331B2
Reaction notes
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