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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643007Generated: November 1, 2026

Water → 2-(4-(azidomethyl)-1H-imidazol-1-yl)-5-bromopyridine

https://huagongshe.com/reaction/643007

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantThionyl ChlorideHCID 24386—
ReactantSodium AzideHCID 33557—
Reactant(1-(5-bromopyridin-2-yl)-1H-imidazol-4-yl)methanolHCID 68511931—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product2-(4-(azidomethyl)-1H-imidazol-1-yl)-5-bromopyridineHCID 8661400687.4%

Reaction Steps

To a suspension of (1-(5-bromopyridin-2-yl)-1H-imidazol-4-yl)methanol (520 mg, 2.05 mmol) in CH3CN (5 mL) at room temperature was added SOCl2 (2.5 mL). With the addition, the suspension became clear. After 10 min of stirring, the mixture was concentrated in vacuo. The residue was dissolved in DMF (12 mL), and NaN3 (565 mg, 8.69 mmol) was added. The mixture was stirred at room temperature overnight. H2O and EtOAc were added. The organic phase was separated, washed with 5% NaHCO3, dried over Na2SO4, concentrated in vacuo to give 2-(4-(azidomethyl)-1H-imidazol-1-yl)-5-bromopyridine (500 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696352B2
Source datasetuspto-grants-2010_04
ORD IDord-29979b9fd74c48948f8607ff06295fb7
Source noteuspto-grants-2010_04