Synthesis of an Oxathiolane Drug Substance Intermediate Guided by Constraint Driven Innovation

02 April 2020, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

A new route was developed for construction of the oxathiolane intermediate used in the synthesis of lamivudine (3TC) and emtricitabine (FTC). We developed the presented route by constraining ourselves to low cost, widely available starting materials – we refer to this as supply centered synthesis. Sulfenyl chloride chemistry was used to construct the framework for the oxathiolane from acyclic precurors. This bond construction choice enabled the use of chloroacetic acid, vinyl acetate, sodium thiosulfate and water to produce the oxathiolane.

Keywords

oxathiolane nucleosides
Antiviral
lamivudine
Emtricitabine
Active Pharmaceutical Ingredient Production

Supplementary materials

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Title
2020 03 31 Sulfenyl chloride SI FINAL
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