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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1847233Generated: October 30, 2026

C16H22F6IN2P → 3-(4-Fluoro-phenyl)-4-hydroxy-7-iodo-isothiazolo[5,4-c]pyridine-5-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1847233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantC16H22F6IN2PHCID 46863890—
Reactant3-(4-Fluoro-phenyl)-4-hydroxy-isothiazolo[5,4-c]pyridine-5-carboxylic acid ethyl esterHCID 136344010—
SolventDichloromethaneHCID 6344—
Product3-(4-Fluoro-phenyl)-4-hydroxy-7-iodo-isothiazolo[5,4-c]pyridine-5-carboxylic acid ethyl esterHCID 13641357568.8%

Reaction Steps

To a solution of 3-(4-fluoro-phenyl)-4-hydroxy-isothiazolo[5,4-c]pyridine-5-carboxylic acid ethyl ester (400 mg, 1.25 mmol) in CH2Cl2 (12.5 mL) was added bis(2,4,6-trimethylpyridine)iodine(I) hexafluorophosphate (1.29 g, 2.51 mmol). The reaction mixture was allowed to stir at r.t. for 20 h. Then the mixture was filtered and the filtrate was concentrated in vacuo. The residue was purified by flash column chromatography on silica gel. Elution with 0-20% EtOAc/CH2Cl2, gave the title product (382 mg) as a yellow solid: MS (m/z) 442.9 (M−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952160B2
Source datasetuspto-grants-2015_02
ORD IDord-5658e0caf3374e50a5397ad485479dcd
Source noteuspto-grants-2015_02