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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803824Generated: November 3, 2026

Hydrochloric Acid → HCID 59552587, compound

https://huagongshe.com/reaction/1803824

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium AzideHCID 33557—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 59552404HCID 59552404—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 59552587HCID 59552587—

Reaction Conditions

Temperature23 °C

Reaction Steps

To a stirring solution of the amide 143 (8.8 g, 16 mmol) in dioxane (20 mL) at 23° C. was added a solution of 4 M HCl in dioxane (320 mL). The mixture was stirred for 9 h and concentrated in vacuo to afford a crude, clear, viscous pale-yellow oil. A slurry of NaN3 (1.56 g, 24 mmol) in pyridine (25 mL) was then cooled to 0° C. and trifluoromethanesulfonic anhydride (4 mL, 24 mmol) was added dropwise before allowing the mixture to warm to 23° C. and stir for 3 h. A solution of the amine hydrochloride (6.4 g, 16 mmol) in H2O (11 mL) was then added followed by CuSO4.5H2O (600 mg, 2.4 mmol). The combined mixture was allowed to stir at 23° C. overnight. An aqueous saturated solution of NaHCO3 was then added and the organic layer was extracted 3×EtOAc. The combined organic extracts were washed 1×10% CuSO4, 2×1 M HCl, 1×brine, and dried over MgSO4. Solvents were removed in vacuo and the crude residue purified by flash chromatgraphy on silica gel using hexanes/ethyl actetate on a Biotage purification system yielding the azide 144 as a colorless, viscous oil (3.3 g, 53%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354092B2
Source datasetuspto-grants-2013_01
ORD IDord-174aad1bcb6c4f2c95bb8fb4ca40bc5e
Source noteuspto-grants-2013_01