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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 559545Generated: October 30, 2026

Sodium Azide → HCID 86616332, compound

https://huagongshe.com/reaction/559545

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
ReactantTrimethylsilyldiazomethaneHCID 167693—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 66974111HCID 66974111—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
SolventThionyl ChlorideHCID 24386—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86616332HCID 86616332—

Reaction Steps

To a solution of 2-(4-(hydroxymethyl)-1H-imidazol-1-yl)-5-(2-oxopyridin-1(2H)-yl)benzoic acid prepared above (92 mg, 0.30 mmol) in MeOH (4 mL) and dioxane (2 mL) at room temperature, (trimethylsilyl)diazomethane (2 M in ether, 0.30 mL, 0.60 mmol) was added. After the mixture was stirred at room temperature overnight, more (trimethylsilyl)diazomethane (2 M in ether, 0.40 mL, 0.80 mmol) was added. After stirring for another day, the solution was concentrated in vacuo to give a residue. The residue was dissolved in SOCl2 (4 mL). The solution was stirred at room temperature for 20 min before it was concentrated in vacuo to give a residue, which was then dissolved in DMF (3 mL). To the solution, NaN3 (65 mg, 1.0 mmol) was added. After the mixture was stirred at room temperature for 2 h, water and EtOAc were added, then 5% aq. NaHCO3 was added. The organic layer was separated, dried over Na2SO4, concentrated in vacuo to give methyl 2-(4-(azidomethyl)-1H-imidazol-1-yl)-5-(2-oxopyridin-1(2H)-yl)benzoate (25 mg). MS 351.1 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063077B2
Source datasetuspto-grants-2011_11
ORD IDord-d3cb58cb66ca4db6a933b6e15d3617f2
Source noteuspto-grants-2011_11