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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1398682Generated: October 27, 2026

2-Fluoroethanol → 4-[2-(2-fluoroethoxy)-6-iodo-1H-1,3-benzodiazol-1-yl]pyrimidin-2-amine

https://huagongshe.com/reaction/1398682

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-FluoroethanolHCID 9737—
ReactantCesium carbonateHCID 10796—
Reactant4-[6-iodo-2-(trichloromethyl)-1H-1,3-benzodiazol-1-yl]pyrimidin-2-amineHCID 68181943—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-[2-(2-fluoroethoxy)-6-iodo-1H-1,3-benzodiazol-1-yl]pyrimidin-2-amineHCID 8666960917.1%

Reaction Steps

A solution of 4-[6-iodo-2-(trichloromethyl)-1H-1,3-benzodiazol-1-yl]pyrimidin-2-amine (1 g, 2.20 mmol), 2-fluoroethan-1-ol (900 mg, 14.05 mmol) and cesium carbonate (4.3 g, 13.20 mmol) in N,N-dimethylformamide (10 mL) was stirred for 14 hr at room temperature. The reaction mixture was diluted with 50 mL of ethyl acetate then washed with 5×10 mL of water. The organic layer was dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was purified on a silica gel column (ethyl acetate/petroleum ether, 10:1) to afford 150 mg (17%) of 4-[2-(2-fluoroethoxy)-6-iodo-1H-1,3-benzodiazol-1-yl]pyrimidin-2-amine as brown oil: LC-MS: m/z=400 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901313B2
Source datasetuspto-grants-2014_12
ORD IDord-1282d28e986c460f9ec44bc0b75b9d28
Source noteuspto-grants-2014_12