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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1089420Generated: October 31, 2026

Benzoyl chloride → N4,2'-O,3'-O-tribenzoyl-5'-deoxy-5-fluorocytidine

https://huagongshe.com/reaction/1089420

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
Reactant5'-Deoxy-5-fluorocytidineHCID 10037499—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventPyridineHCID 1049—
ProductN4,2'-O,3'-O-tribenzoyl-5'-deoxy-5-fluorocytidineHCID 53982579—

Reaction Steps

5'-Deoxy-5-fluorocytidine (245 mg), benzoyl chloride (400 μl) and 4-dimethylaminopyridine (122 mg) were dissolved in dry pyridine (5 ml). After stirring for 3 hours at room temperature pyridine was removed under reduced pressure. The residue was partitioned between ethyl acetate and water. The ethyl acetate layer was dried over magnesium sulfate and concentrated under reduced pressure. The residue was recrystallized from methanol to give N4,2'-O,3'-O-tribenzoyl-5'-deoxy-5-fluorocytidine (280 mg), mp 158°~160° C.; MS 558 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04966891
Source datasetuspto-grants-1990_10
ORD IDord-6f80ff6256fc479cad8ec2f262acf0a0
Source noteuspto-grants-1990_10