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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416146Generated: November 2, 2026

Uridine → HCID 69539402, compound

https://huagongshe.com/reaction/2416146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantUridineHCID 6029—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantDabcoHCID 9237—
ReactantHCID 69539405HCID 69539405—
SolventAcetonitrileHCID 6342—
SolventTriethylamineHCID 8471—
ProductHCID 69539402HCID 6953940275.2%

Reaction Steps

To 2.0 g of 3′,5′-O-bis(4-chlorobenzoyl)-2′-deoxyuridine was added 60 mL of acetonitrile, 0.81 g of triethylamine, 0.54 g (1.2 times moles based on the uridine derivative) of 1,4-diazabicyclo[2.2.2]octane and 1.5 g of p-toluenesulfonyl chloride, and the resulting mixture was stirred at room temperature for 3 hours. Ammonia gas was bubbled into the reaction mixture at room temperature for 1 hour, and the mixture was stirred in an ice bath for 30 minutes. The crystals were filtered and washed with acetonitrile to give 1.52 g of 3′,5′-O-bis(4-chlorobenzoyl)-2′-deoxycytidine. Yield 75.2%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06822090B2
Source datasetuspto-grants-2004_11
ORD IDord-2fe7c47b59714efd95caa7d6974b9d68
Source noteuspto-grants-2004_11