Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1891891Generated: October 31, 2026

N-Iodosuccinimide → 2-Amino-5-fluoro-3-iodopyridine

https://huagongshe.com/reaction/1891891

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
ReactantSodium BicarbonateHCID 516892—
ReactantAcetic acid 10-acetoxymethyl-anthracen-9-ylmethyl esterHCID 613145—
Reactant2-Amino-5-fluoropyridineHCID 2737701—
SolventDimethyl SulfoxideHCID 679—
Product2-Amino-5-fluoro-3-iodopyridineHCID 1845597418%

Reaction Steps

To a mixture of 2-amino-5-fluoropryidine (2.0 g, 17.8 mmol) and dimethyl sulfoxide (50 mL) was added N-iodosuccinimide (4.8 g, 21.4 mmol), which was stirred for 1 hour at room temperature. A suitable amount of acetic add was added to this mixture, which was stirred for 1 hour at the same temperature, and then stirred for another 3 hours at 55° C. This reaction mixture was cooled to room temperature, after which a saturated sodium hydrogencarbonate aqueous solution was added, and the mixture was extracted with ethyl acetate. The organic layer was separated, washed with water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure, and the residue thus obtained was purified by NH silica gel column chromatography (ethyl acetate) to obtain the title compound (751 mg, 18%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507530B2
Source datasetuspto-grants-2013_08
ORD IDord-07e5cd7483ad4e5c98825a4e0c8644d5
Source noteuspto-grants-2013_08