“…The crude mixture was purified by flash column chromatography (DCM:MeOH 0-10%) affording the title compound as a white solid (37.1 mg, 0.049 mmol, 29%); 1 H NMR (500 MHz, Chloroform-d) d 10.20 (bs, 1H), 8.46 (dt, J ¼ 6.9, 3.8 Hz, 1H), 7.79 À 7.67 (m, 3H), 7. 133.7, 131.8, 131.7, 129.5, 129.3, 128.4, 127.9, 127.3, 126.6, 125.0, 123.7 (d, J ¼ 17.8 Hz, 1 C), 116.3 (d, J ¼ 25.2 Hz, 1 C), 47.4 (2 C), 42.3 (2 C), 37.7, 29.0 (3 C), 27.3 (3 C), 13.7 (3 C), 9.6 (3 C); 19 F (Yang et al 2012 To a 1.5 mL microcentrifuge tube was added 4-(4-fluoro-3-(4-(3-(tributylstannyl)benzoyl)piperazine-1-carbonyl)benzyl) phthalazin-1(2H)-one (100 mg, 0.132 mmol) in anhydrous MeCN (10 mL), N-Chlorosuccinimide (NCS) (50 mg, 0.37 mmol) in a solution of anhydrous methanol (25 mL), acetic acid (10 mL), anhydrous acetonitrile (20 mL) and 123 I-NaI in NaOH 0.1 M (0.34-0.41 GBq, 9.29-11.04 mCi). After addition, the reaction was stirred at 650 rpm for 15 min at 25 C. The crude reaction was purified by RP-HPLC (C18 Waters Atlantis T3) column (C18-RP, 5 mm, 6 Â 250 mm) Solvent A: H 2 O, Solvent B: MeCN; flow rate: 1 mL/min; gradient: 0-5 min 5% B; 5-15 min 5-95% B; 15-18 min 95% B; 18-20 min 95 À 5% B).…”