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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1886515Generated: October 25, 2026

Triphosphate → 1-(2-Hydroxyethoxymethyl)5-(3-amino-1-propynyl)cytosine

https://huagongshe.com/reaction/1886515

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphosphateHCID 3440921—
Reactant1-(2-Hydroxyethoxymethyl)-5-(3-trifluoroacetamido-1-propynyl)cytosineHCID 19958018—
Product1-(2-Hydroxyethoxymethyl)5-(3-amino-1-propynyl)cytosineHCID 19876338—

Reaction Steps

The hydroxyl group of the sugar part of alkynylamino nucleoside 69 (0.167 mmol) was converted to a triphosphate and the trifluoroacetyl group was removed following the general procedure given in Example 1E. After addition of the second aliquot of phosphorus oxychloride, phosphorylation was allowed to proceed for for 75 min. Assuming an absorption coefficient for the product equal to that of the starting material (7,790), the yield of triphosphate 67, based on its UV absorption at 291 nm, was 21%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05151507
Source datasetuspto-grants-1992_09
ORD IDord-af9848824da5406e80396e01c8eacb82
Source noteuspto-grants-1992_09