Citrate → [(2S,3S,5R)-5-(2-amino-6-ethoxy-purin-9-yl)-3-azido-tetrahydrofuran-2-yl]methanol

Beteiligte Stoffe

Reaktionsbedingungen

Reaktionsschritte

To 500 mL of an aqueous pH 6.0, 50 mM citrate buffer, prepared as described in Example 2c, was added 2-amino-6-ethoxypurine (0.0895 g, 0.5 mmol) and 3'-azido-3'-deoxythymidine (0.668 g, 2.5 mmol). Solution was achieved by heating the mixture at 50° C. with sonication. A sample was removed as a control. A 24 mL solution of trans-N-deoxyribosylase (Example 2b) at an activity of 1400 units/mL was added. The reaction was heated at 50° C. Four days later 0.089 g, 0.5 mmol, of 2-amino-6-ethoxypurine was added to the reaction. The reaction was terminated after eleven days. The reaction was heated to 80° C. to precipitate the enzyme and then filtered. The aqueous solution was extracted with ethyl acetate to remove the product. The combined ethyl acetate fractions were dried with magnesium sulfate, filtered and the solvent removed in vacuo to give a foam. The foam was chromatographed on 180 g of silica gel (230-400 mesh) eluted with chloroform/methanol (98:2. v/v). The product containing fractions were combined and the solvent removed in vacuo to give the product as an oil. The oil was dissolved in water and lyophilized to give a solid (55% yield).

Herkunft & Nachweise