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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1886505Generated: October 26, 2026

Iodine → 2',3'-Dideoxy-5-iodocytidine

https://huagongshe.com/reaction/1886505

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantDideoxycytidineHCID 24066—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product2',3'-Dideoxy-5-iodocytidineHCID 1463010483%

Reaction Steps

A solution of 2',3'-dideoxycytidine (2.11 g, 10 mmol, Raylo) and mercuric acetate (3.35 g, 10.5 mmol, Fisher) in 50 mL of methanol was refluxed for 19 h. The resulting white suspension was diluted with methanol (50 mL) and dichloromethane (100 mL). Iodine (3.05 g, 12 mmol) was added and the suspension was stirred at 25° until a clear purple solution was present. After 4 h, the free base form of AG3 X4A resin (20 mL, 38 meq, Bio-Rad; a weakly basic polystyrene resin) was added and hydrogen sulfide was bubbled into the reaction for 15 min. Complete precipitation of mercury(II) was verified by TLC. The reaction was filtered though filter aid and the filter aid was washed with 1:1 methanol-dichloromethane. The filtrate was evaporated onto silica gel 10 g) and the loaded silica gel was placed on top of a 150 g silica gel column. Elution with 5%, 10% and 20% methanol in dichloromethane afforded 2.79 g (83%) of iodide 44 as a colorless crystalline solid. Two recrystallizations from boiling water afforded, after vacuum-drying at 50°, large, analytically-pure prisms (mp: d 178°).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05151507
Source datasetuspto-grants-1992_09
ORD IDord-66548818be4c47bbab69c33fbed860eb
Source noteuspto-grants-1992_09