Dimethylformamide → 5-(6-(6-amino-9-(3-(isopropylamino)propyl)-9H-purin-8-ylthio)benzo[d][1,3]dioxol-5-yl)furan-2-carbaldehyde

Participants

Reaction Conditions

Reaction Steps

2-Formyl-5-furanylboronic acid (12.3 mg, 0.0877 mmol) was added to PU-H71 (30 mg, 0.0585 mmol) and NaHCO3 (14.7 mg, 0.1755 mmol). DMF (1 mL) was added and the reaction mixture was evacuated and back filled with nitrogen. This was repeated four times then nitrogen was bubbled through the reaction mixture for 10 minutes. Then H2O (0.1 mL) and Pd(PPh3)2Cl2 (4 mg, 0.00584 mmol) were added and the reaction mixture was heated under nitrogen at 90° C. for 4 h. Solvent was removed under reduced pressure and the resulting residue was purified by preparatory TLC (hexane:CH2Cl2:EtOAc:MeOH—NH3 (7N), 2:2:1:0.5) to give 9.5 mg (34%) of DZ3-33. 1H NMR (500 MHz, CDCl3/MeOH-d4) δ 9.57 (s, 1H), 8.18 (s, 1H), 7.36 (d, J=3.8 Hz, 1H), 7.32 (s, 1H), 7.07 (s, 1H), 6.98 (d, J=3.8 Hz, 1H), 6.12 (s, 2H), 4.32 (t, J=6.7 Hz, 2H), 3.31 (septet, J=6.6 Hz, 1H), 2.93 (t, J=6.8 Hz, 2H), 2.30 (m, 2H), 1.42 (d, J=6.6 Hz, 6H); 13C NMR (125 MHz, CDCl3/MeOH-d4) δ 177.5, 156.8, 154.5, 152.2, 151.9, 151.4, 150.1, 149.7, 148.1, 127.5, 124.3, 119.2, 118.7, 115.7, 112.7, 109.9, 102.9, 51.3, 41.8, 40.4, 26.4, 19.2; HRMS (ESI) m/z [M+H]+ calcd. for C23H25N6O4S, 481.1658; found. 481.1657; HPLC: method A Rt=5.87, method B Rt=5.93.

Provenance & Evidence