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2 protocols using waters 2545 binary gradient module

1

Analytical Characterization of Synthetic Compounds

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Starting materials and other reagents were purchased from commercial suppliers and were used without further purification unless otherwise noted. All reactions were monitored by thin layer chromatography (TLC) with 0.25 mm E. Merck pre-coated silica gel plates (60 F254) and Waters LCMS system (Waters 2489 UV/Visible Detector, Waters 3100 Mass, Waters 515 HPLC pump, Waters 2545 Binary Gradient Module, Waters Reagent Manager, Waters 2767 Sample Manager) using SunFireTM C18 column (4.6 × 50 mm, 5 μm particle size): solvent gradient = 100% A at 0 min, 1% A at 5 min; solvent A = 0.035% TFA in Water; solvent B = 0.035% TFA in CH3CN; flow rate : 2.5 mL/min. Purification of reaction products was carried out by flash chromatography using CombiFlash®Rf with Teledyne Isco RediSep®Rf High Performance Gold or Silicycle SiliaSepTM High Performance columns (4 g, 12 g, 24 g, 40 g, 80 g, or 120 g). The purity of all compounds was over 95% and was analyzed with Waters LCMS system. 1H NMR and 13C NMR spectra were obtained using a Varian Inova-400 (400 MHz for 1H, and 75 MHz for 13C) spectrometer. Chemical shifts are reported relative to chloroform (δ = 7.24) for 1H NMR or dimethyl sulfoxide (δ = 2.50) for 1H NMR and dimethyl sulfoxide (δ = 39.51) for 13C NMR. Data are reported as (br = broad, s = singlet, d = doublet, t = triplet, q = quartet, m = multiplet).
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2

Purification and Characterization of Organic Compounds

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The intermediate compounds as well as the target compounds were purified by flash column chromatography using silica gel 60 (0.040-0.063 mm, 230-400 mesh ASTM)
and technical grade solvents. 1 H NMR and 13 C NMR analyses were carried out on a Bruker Avance 400 spectrometer using tetramethylsilane (TMS) as an internal standard. Melting points were measured on a Walden Precision Apparatus Electrothermal 9300 apparatus and were uncorrected. LC-MS analysis was conducted using the following system: Waters 2998 photodiode array detector, Waters 3100 mass detector, Waters SFO system fluidics organizer, Waters 2545 binary gradient module, Waters reagent manager, Waters 2767 sample manager, Sunfire™ C 18 column (4.6 × 50 mm, 5 μm particle size); Solvent gradient = 95% A at 0 min, 1% A at 5 min; solvent A: 0.035% trifluoroacetic acid (TFA) in water; solvent B: 0.035% TFA in MeOH; flow rate = 3.0 mL/min; the AUC was calculated using Waters MassLynx 4.1 software. The solvents and liquid reagents were transferred using hypodermic syringes. All the solvents and reagents were purchased from commercial companies, and used as such.
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