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Enantioselective Hydrogenation of dehydro-PZQ and derivatives
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14th April 2011 @ 08:12
Preparation of N-benzoyl-PZQ as starting material for an oxidative dehydrogenation [data=size:500x180]1061[/data] [b]Hazard and Risk Assessment:[/b] [data]1043[/data] Start time: 6:30 PM 14/04/2011 End time: 9:15 AM 15/04/2011 To an ice-cooled solution of [url=http://www.ourexperiment.org/enantio_hydgen/1946][i]rac[/i]-PZQamine[/url] (3.23 g, 16.0 mmol, M.W. = 202.3 g/mol) and triethylamine (2.43g, 24.0 mmol,3.35 mL, 1.5 eq., M.W. 101.2, d=0.726 g/mL) in DCM (60 mL) was added benzoyl chloride (3.38 g, 24.0 mmol, 2.80 mL, 1.5 eq., M.W. = 140.6 g/mol, d=1.21 g/mL) at 0°C and stirred at room temperature for 15 h. The reaction was quenched with water and stirred for a further 30 min. The mixture was neutralized with sodium hydrogen carbonate solution and the layers were separated. The organic layer was washed with sodium hydrogen carbonate solution and dried over magnesium sulfate. After evaporation of the solvent a yellow solid remained. - crude yield: 6.42 g (21.0 mmol, 131%) [M.W. 306.4 g/mol] TLC (ethyl acetate, stain: ninhydrin, KMnO4) [data]1075[/data] - recrystallized from toluene (70 mL), filtered, dried under vac.: yield: 4.69 g (15.3 mmol, 96%) colourless solid, still toluene impurities -> high vac [u]Yield:[/u] 4.10 g (13.4 mmol, 84%) - filtrate evaporated, remaining orange solid recrystallized a second time from toluene (20 mL) [u]Yield:[/u] 520 mg (1.70 mmol, 11%) [b]Result:[/b] Over-all yield: 4.62 g (15.1 mmol, 94%) [b]Analytical data:[/b] Rf (ethyl acetate, 100%) = 0.45. m.p. 157-158.5°C (recrystallized from toluene) (lit. 158-160°C (acetone) [1]) 1H NMR (CDCl3, 200 MHz): δ = 2.74-3.10 (m, 4H), 4.02-4.10 (m, 1H), 4.40 (br m, 1H), 4.80-5.00 (m, 2H), 5.19 (br m, 1 H), 7.21 (m, 4H), 7.48 (m, 5H). 13C NMR (CDCl3, 50.3 MHz): δ = 28.8, 39.0, 45.8 (br), 51.5 (br), 54.9 (br), 125.4 (br), 127.0, 127.4 (br, 2 C), 127.5, 128.8 (2 C), 129.5, 130.7, 132.5 (br), 134.4 (br), 135.0, 164.4, 170.3. IR (neat): nu = 1786 cm-1, 1611, 1420, 1289, 1247, 1212, 1036, 760, 718, 698, 656. MS (ESI (+)) m/z (%): 635 (100, [M2+Na]+), 329 (28, [M+Na]+). HRMS (ESI (+)) Calcd. for [C19H18N2O2+Na]+: 329.12605, found: 329.12619. HPLC: Chiralcel OD-H, hexane/iso-propanol/Et3N = 60/40/0.1, 0.7 ml/min flow rate, RT: 24.8 min, 31.5 min.[data=text]1107[/data] HPLC: Chiralcel OD-H, hexane/iso-propanol/Et3N = 70/30/0.1, 0.7 ml/min flow rate, RT: 30.2 min, 38.3 min. [data=text]1110[/data] [data]1095[/data][data]1071[/data][data]1077[/data][data]1105[/data] Starting material for: [*] [url=http://www.ourexperiment.org/enantio_hydgen/1962]Oxidation of N-benzoyl-PZQ by sulfur (MW59-1 to MW59-6)[/url] [*] [url=http://www.ourexperiment.org/enantio_hydgen/1993]Scale-up: Oxidation of N-benzoyl-PZQ by sulfur (MW59-7)[/url] [b]References:[/b] [url=http://onlinelibrary.wiley.com/doi/10.1002/ardp.19893221104/abstract][1] Spectral and Chemical Properties of Pyrazino-[2,1-a]-isoquinolin-4-one Derivatives, K. Kiec'-Kononowicz, [i]Arch. Pharm.[/i] [b]1989[/b], [i]322[/i],795-799. DOI: 10.1002/ardp.19893221104.[/url]
Attached Files
Scheme MW58.png
1H MW58-1.dx
13C NMR MW58-1 (lb_2).pdf
1H NMR MW58-1.pdf
TLC MW58-1a.jpg
13C NMR MW58-1 (lb=6).pdf
13C MW58-1.dx
1H NMR MW58-1.pdf
IR MW58-1.pdf
HPLC MW58-1 (40_60_01).jpg
HPLC MW58 (30_70_01).jpg