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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1050760Generated: November 2, 2026

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

https://huagongshe.com/reaction/1050760

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 numberUS09387200B2
Source datasetuspto-grants-2016_07
ORD IDord-1679f6bab23f4783a9a092cf3436e90a
Source noteuspto-grants-2016_07