86118-11-8

98026-05-2

4219-94-7

The general procedure for the synthesis of O-methyl DL-serine from 2-amino-3-methoxypropionamide was as follows: in small-scale experiments, ACL racemase (Locus: E01594) and PepB (Locus: D84499) were added to an aqueous solution containing α-amino-β-methoxypropionamide (4). The reaction mixture (20 mL) contained 2 mM pyridoxal 5'-phosphate (PLP), 0.1 M potassium phosphate buffer (KPB, pH 9.0), and 0.5 mol/L α-amino-β-methoxypropionamide (4). Subsequently, ACL racemization enzyme (3.0 mg) and PepB (1.2 mg) were added, and the reaction was incubated for 18 h at 38°C. The progress of the reaction was monitored by periodic sampling. D/L-α-amino-β-methoxyalanamide (4) and O-methyl-L-serine (5) were determined using HPLC equipped with a Crownpak CR(+) column at a flow rate of 0.5 mL/min employing 50 mM HClO4 as a solvent system, and the absorbance of the eluate was monitored at 210 nm. Upon completion of the reaction, O-methyl-L-serine (5) was obtained by deproteinization with trichloroacetic acid and separation by Dowex-X8 (H+) column chromatography. The isolated O-methyl-L-serine (5) (7.98 mmol, 950 mg) was recrystallized from a mixed solvent of water-methanol-isopropanol-ether to give white crystals with an enol purity of >99.9%. The product has a melting point of 211-213 °C (decomposition) and a specific rotation of 1/25D (c 1, 6 mol/L HCl).1H NMR (400 MHz, D2O) data: δ 3.24 (s, 3H), 3.78-3.81 (m, 1H), 3.83 (dd, J = 3.5, 9.8 Hz, 1H), 4.01 (dd, J = 6.1, 9.8 Hz, 1H).13C NMR (100 MHz, D2O) data: δ 177.3 (CO), 76.5 (CH2), 60.2 (CH), 56.7 (OCH3). Elemental analysis (C4H9NO3) Calculated values: C, 40.32; H, 7.58; N, 11.75. Measured values: C, 40.35; H, 7.54; N, 11.77. ESI-MS (m/z): 120.1230 [M + H]+.