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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716128Generated: November 1, 2026

N,O-bis(trimethylsilyl)acetamide → HCID 89975754, compound

https://huagongshe.com/reaction/716128

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,O-bis(trimethylsilyl)acetamideHCID 6913588—
ReactantHCID 89975764HCID 89975764—
ReactantCytosineHCID 178418229—
SolventDichloromethaneHCID 6344—
ProductHCID 89975754HCID 89975754—

Reaction Conditions

Temperature80 °C

Reaction Steps

To another reaction vessel, 0.12 g of cytosine and 0.53 mL of N,O-bis(trimethylsilyl)acetamide were added in a nitrogen atmosphere, and the obtained mixture was then stirred at 80° C. for 2 hours. After cooling in air, a methylene chloride solution containing (3S,4S,5R)-2-bromo-4-((4-chlorobenzyl)oxy)-5-(((4-chlorobenzyl)oxy)methyl)-3-fluorothiolane was added to the reaction mixture, and the obtained mixture was then stirred 60° C. for 2 hours. Thereafter, methylene chloride was added to the reaction mixture, and the thus obtained mixture was washed with a saturated sodium hydrogen carbonate aqueous solution, and was then dried over anhydrous sodium sulfate. After that, the solvent was distilled away under reduced pressure. The obtained residue was purified by silica gel column chromatography (chloroform/methanol=100/0 to 80/20), so as to obtain 0.18 g of (3S,4S,5R)-2-(4-amino-2-oxo-1,2-dihydropyrimidin-1-yl)-4-((4-chlorobenzyl)oxy)-5-(((4-chlorobenzyl)oxy)methyl)-3-fluorothiolane in the form of a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187514B2
Source datasetuspto-grants-2015_11
ORD IDord-e16e6b2839db402ebdaa2bba0ad7d32c
Source noteuspto-grants-2015_11