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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 465720Generated: October 30, 2026

Citrate → HCID 476443, compound

https://huagongshe.com/reaction/465720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitrateHCID 31348—
ReactantZidovudineHCID 35370—
ReactantHCID 178508848HCID 178508848—
ProductHCID 476443HCID 47644354%

Reaction Conditions

Temperature50 °C

Reaction Steps

To 800 mL of an aqueous pH 6.0, 50 mm citrate buffer, prepared as described in Example 2c' was added 2-amino-6-phenoxy-9H-purine (0.181 g, 0.8 mmol) and 3'-azido-3'-deoxythymidine (1.069 g, 4.0 mmol). Solution was achieved by heating the mixture at 50° C. with sonication. A sample was removed as a control. A 40 mL solution of trans-N-deoxyribosylase (Example 2b) with an activity of 1500 units/mL was added. The reaction was heated at 50° C. Six days later, 0.181 g, 0.8 mmol, of 2-amino-6-phenoxypurine was added to the reaction. Fifteen days after the reaction was started, another 0.181 g, 0.8 mmol, of 2-amino-6-phenoxypurine and 0.428 g, 1.6 mmol, of 3'-azido-3'-deoxythymidine were added to the reaction. The reaction was stopped after thirty-three days, by heating to 80° C. to precipitate the enzyme, and 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 basic alumina grade 1 eluted with chloroform/methanol (99:1, v/v). The fractions containing product were combined and the solvent removed in vacuo to give the product as a foam, 0.48 g, 54% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05153318
Source datasetuspto-grants-1992_10
ORD IDord-e1b0d82dd8244da0b57b5a3e11e0d047
Source noteuspto-grants-1992_10