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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720557Generated: November 2, 2026

Uracil → HCID 10670845, compound

https://huagongshe.com/reaction/1720557

Reaction equation

Participants

RoleNameHCIDCharge
ReactantUracilHCID 1174—
ReactantTin tetrachlorideHCID 24287—
Reactantbeta-D-Glucose pentaacetateHCID 2724702—
Solvent1,2-DichloroethaneHCID 11—
SolventBenzeneHCID 241—
ProductHCID 10670845HCID 10670845—

Reaction Steps

Uracil is bis-trimethylsilylated according to the procedure of Niedballa and Vorbruggeno Uracil is dissolved in benzene, and added to 1,2,3,4,6-penta-O-acetyl-β-D-glucopyranose 33.1b (Xi=β-OAc) (Niedbala and Vorbruggen) in 1,2 dichloroethane followed by tin tetrachloride in 1,2-dichloroethane according to the method of Vorbruggen and Niedballa to provide the 1-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)uracil 33.1b (Xi=β-uracil-1-yl). Following methanolysis with sodium methoxide in methanol the 1-(B-D-glucopyranosyl)uracil 33.1a (Xi=β-uracil-1-yl) is obtained. This is converted into the morpholino subunit 32.2b (Xi=β-uracil-1-yl) by the general procedure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05506337
Source datasetuspto-grants-1996_04
ORD IDord-46645776da004e07b2b86cde78eb70b5
Source noteuspto-grants-1996_04