Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1780691Generated: October 26, 2026

Water → 2-Azidohexadecanoic acid

https://huagongshe.com/reaction/1780691

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium AzideHCID 33557—
Reactant2-Bromohexadecanoic acidHCID 82145—
SolventDimethylformamideHCID 6228—
Product2-Azidohexadecanoic acidHCID 1904720982.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

To the solution of 2-bromohexadecanoic acid (1.00 g) in N,N-dimethylformamide (DMF, 15 ml) was added sodium azide (0.86 g), and the mixture was stirred at 80° C. for 12 hours. To the reaction mixture, after having been cooled to room temperature, was then added water. The mixture was extracted with ethyl acetate, and the ethyl acetate layer was separated, washed twice with brine, dried over anhydrous sodium sulfate. The solvent was removed by distillation to give 2-azidohexadecanoic acid (0.73 g). To the solution of 2-azidohexadecanoic acid in DMF were added N-hydroxysuccinimide (74 mg) and N,N'-dicyclohexylcarbodiimide (146 mg), and the mixture was stirred for 12 hours. Precipitates produced was removed by filtration, and the filtrate was concentrated to give the active ester of 2-azidohexadecanoic acid. To the active ester in DMF were further added 6-(4'-N-glycyl-spicaminyl-amino)purine hydrochloride (246 mg) and triethylamine (0.72 ml), and the mixture was stirred for 12 hours. The solvent was removed by distillation, and the residue was subjected to chromatography on a silica gel column with an eluent system of chloroform-methanol (6:1) to give SPK229 in the yield of 185 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05631238
Source datasetuspto-grants-1997_05
ORD IDord-f50abf435675470f8abad3da99bb1384
Source noteuspto-grants-1997_05