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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2210219Generated: November 1, 2026

5-Fluorouridine → Floxuridine

https://huagongshe.com/reaction/2210219

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-FluorouridineHCID 9427—
Reactant1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene)HCID 96831—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductFloxuridineHCID 5790—

Reaction Steps

5.244 gins. (20 mMoles) of 5-fluorouridine is dissolved in 20 mL anhydrous pyridine and then dried under vacuum. This procedure is repeated at least one more time in order to make 5-fluorouridine devoid of moisture. The dried 5-fluorouridine is then dissolved in 20 mL of pyridine. 8.131 gms (24 mMoles, 1.2 eq.) of 4,4'-dimethoxy trityl chloride is added as solid in 4 fractions over a period of 2 hours. The reaction mixture is then stirred at room temperature overnight and is then diluted with 25 mL of dichloromethane and washed with saturated sodium bicarbonate solution. The aqueous layer is then washed with 20mL dichloromethane. The organic layers are mixed and washed with saturated bicarbonate solution two more times. The organic layer is then dried over anhydrous sodium sulphate. The solvent is removed under vacuum to yield a yellow foam which is purified on a silica gel column using 90:10 chloroform:methanol as eluent. The 4, 4'-dimethoxytrityl derivative of 5-fluorodeoxyuridine is prepared in an analogous manner.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05457187
Source datasetuspto-grants-1995_10
ORD IDord-eaa5f6ee2d9c43b2b1cf5c48a6c63ec2
Source noteuspto-grants-1995_10