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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1629224Generated: November 2, 2026

Water → HCID 178456683, compound

https://huagongshe.com/reaction/1629224

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium BicarbonateHCID 516893—
Reactant4-Bromo-2-fluorobenzimidamide hydrochlorideHCID 53407891—
Reactant2-bromo-1-[1-(propan-2-yl)-1H-1,2,4-triazol-5-yl]ethan-1-oneHCID 58204489—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178456683HCID 17845668374.3%

Reaction Steps

To a rapidly stirred mixture of 4-bromo-2-fluoro-benzamidine hydrochloride (9.84 g, 38.8 mmol), potassium hydrogen carbonate (15.6 g, 154.8 mmol), THF (98 mL) and water (16 mL) at reflux was added a solution of 2-bromo-1-(2-isopropyl-2H-[1,2,4]triazol-3-yl)-ethanone (9.0 g, 38.8 mmol) in THF (19 mL) over 15 min. The resulting mixture was stirred for 18 h at reflux before concentrating in vacuo. The resultant residue was treated with water and the solid formed collected by filtration, washed (water, then 1:1 diethyl ether: cyclohexane then diethyl ether) to give 5-[2-(4-Bromo-2-fluoro-phenyl)-1H-imidazol-4-yl]-1-isopropyl-1H-[1,2,4]triazole as a brown solid (10.1 g, 74%). 1H NMR δ (ppm)(CDCl3): 8.21-8.14 (1 H, m), 7.90 (1 H, s), 7.80 (1 H, s), 7.47-7.38 (2 H, m), 7.26 (1 H, s), 5.91 (1 H, br, s), 1.59 (6 H, d, J=6.63 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785626B2
Source datasetuspto-grants-2014_07
ORD IDord-da248af23a104f989e9bcdc35eb4c3d8
Source noteuspto-grants-2014_07