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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1937722Generated: November 1, 2026

Palmitoyl chloride → 3',5'-Di-palmitoyl-2'-deoxy-2'-(N-Fmoc-beta-alanineamido)uridine

https://huagongshe.com/reaction/1937722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPalmitoyl chlorideHCID 8206—
Reactant2'-Deoxy-2'-(N-Fmoc-beta-alanineamido)uridineHCID 68661469—
SolventPyridineHCID 1049—
Product3',5'-Di-palmitoyl-2'-deoxy-2'-(N-Fmoc-beta-alanineamido)uridineHCID 8658767165%

Reaction Steps

Palmitoyl chloride (1.55 mL, 1.8 mmol) was added to a solution of nucleoside 28 in abs pyridine and the reaction mixture was stirred overnight at room temperature. The solution was then quenched with MeOH, evaporated to dryness, dissolved in dichloromethane and washed with saturated aq sodium bicarbonate and brine. The organic phase was dried over sodium sulfate and evaporated to dryness. The residue was purified by flash chromatography on silica (EtOAc-Hexanes 1:1) affording 0.5 g of 29 (yield, 65%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06395713B1
Source datasetuspto-grants-2002_05
ORD IDord-6cdfd17635bb413b89901a5e8c450467
Source noteuspto-grants-2002_05