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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1777284Generated: November 2, 2026

Trimethylsilyl triflate → 5-Aza-2'-deoxycytidine

https://huagongshe.com/reaction/1777284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl triflateHCID 65367—
ReactantBis(trimethylsilyl)trifluoroacetamideHCID 94358—
ReactantSodium MethoxideHCID 10942334—
Reactant1-chloro-3,5-di-p-toluoyl-2-deoxy-D-ribofuranoseHCID 67420786—
ReactantHCID 178508820HCID 178508820—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
Product5-Aza-2'-deoxycytidineHCID 45166836.8%

Reaction Steps

34 mL of BSTFA are added to a suspension of 6.4 g of azacytosine in 300 mL of acetonitrile. The mixture is brought to 50° C. and it is stirred for 90 minutes. It is cooled to ambient temperature, 6.3 mL of trimethylsilyltriflate and 11.1 g of 1-chloro-3,5-di-p-toluoyl-2-deoxy-D-ribofuranose are added to the solution, in about ten minutes. It is stirred for 140 minutes, 400 mL of methanol are added controlling the temperature in an ice bath. Concentration is carried out at low pressure until a viscous residue is obtained, 400 mL of methanol are added, it is heated to 50° C. and 36 mL of 30% solution of sodium methylate in methanol are added. It is stirred for 1 hour, it is cooled to 0° C., it is stirred to complete precipitation and the solid is filtered by washing it on the filter with methanol. 2.3 g of decitabine with HPLC purity (UV 254 nm) of 99.2% are obtained after drying at low pressure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266863B2
Source datasetuspto-grants-2016_02
ORD IDord-208bd4b0488f4fc3b89b3c2da543ecc0
Source noteuspto-grants-2016_02