Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416145Generated: November 1, 2026

Ammonia → HCID 69539402, compound

https://huagongshe.com/reaction/2416145

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantUridineHCID 6029—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantN-MethylpiperidineHCID 12291—
ReactantHCID 69539405HCID 69539405—
SolventIsopropanolHCID 3776—
SolventAcetonitrileHCID 6342—
SolventTriethylamineHCID 8471—
ProductHCID 69539402HCID 6953940254%

Reaction Steps

To 1.0 g of 3′,5′-O-bis (4-chlorobenzoyl)-2′-deoxyuridine was added 5 mL of acetonitrile, 0.40 g of triethylamine, 0.24 g (1.2 times moles based on the uridine derivative) of 1-methylpiperidine and 0.76 g of p-toluenesulfonyl chloride, and the reaction mixture was stirred in an ice bath for 2 hours. To this, 7.5 mL of a solution of ammonia in 2-propanol was added, and the mixture was stirred in an ice bath for 4 hours, and at room temperature for 1 hour. The crystals were filtered and washed with acetonitrile to give 0.54 g of 3′,5′-O-bis(4-chlorobenzoyl)-2′-deoxycytidine. Yield 54%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06822090B2
Source datasetuspto-grants-2004_11
ORD IDord-91b52cbdb84c47e4a2dd6c5bd92e10c2
Source noteuspto-grants-2004_11