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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 470175Generated: October 30, 2026

(Diethylamino)sulfur trifluoride → 7-fluoro-1-((1R,4S)-4-fluorocyclopent-2-enyl)-1H-imidazo[4,5-c]pyridin-4-amine

https://huagongshe.com/reaction/470175

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Diethylamino)sulfur trifluorideHCID 123472—
ReactantSodium BicarbonateHCID 516892—
Reactant(1R,4R)-4-(4-amino-7-fluoro-1H-imidazo[4,5-c]pyridin-1-yl)cyclopent-2-enolHCID 58329291—
SolventDichloromethaneHCID 6344—
Product7-fluoro-1-((1R,4S)-4-fluorocyclopent-2-enyl)-1H-imidazo[4,5-c]pyridin-4-amineHCID 58329309—

Reaction Conditions

Temperature0 °C

Reaction Steps

(1R,4R)-4-(4-amino-7-fluoro-1H-imidazo[4,5-c]pyridin-1-yl)cyclopent-2-enol (4-3) (600 mg, 2.6 mmol, 1 eq) was dissolved in DCM (120 mL). The mixture was cooled to 0° C. and DAST (1.6 mL, 12.0 mmol, 4.7 eq) was added. The resulting mixture was stirred at the same temperature for 1 hour. Upon disappearance of starting material, the reaction mixture was poured over NaHCO3 (30 mL) and extracted with CHCl3 (3×50 mL). The combined organics were dried over MgSO4, filtered and concentrated. The crude residue was purified by flash chromatography (0-100% Acetone in DCM) to afford 7-fluoro-1-((1R,4S)-4-fluorocyclopent-2-enyl)-1H-imidazo[4,5-c]pyridin-4-amine (4-5) as a white solid. LRMS m/z (M+H) 236.9.0 found, 237.1 required.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629275B2
Source datasetuspto-grants-2014_01
ORD IDord-2ca1964cfd8d4c58b4fb210623257556
Source noteuspto-grants-2014_01