Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098302Generated: October 27, 2026

Sulfuric Acid → 7-iodo-3-(2-trifluoromethylphenyl)-2H-isoquinolin-1-one

https://huagongshe.com/reaction/1098302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium IodideHCID 5238—
ReactantSodium BicarbonateHCID 516892—
Reactant7-amino-3-(2-trifluoromethylphenyl)-2H-isoquinolin-1-oneHCID 23156738—
ReactantSodium NitriteHCID 23668193—
CatalystCopper iodideHCID 83717—
SolventAcetic AcidHCID 176—
Product7-iodo-3-(2-trifluoromethylphenyl)-2H-isoquinolin-1-oneHCID 2315680390.1%

Reaction Steps

A 1 N sulfuric acid aqueous solution (30 ml) and 862.5 mg (12.5 mmol) of sodium nitrite were added at 0° C. to an acetic acid solution (15 ml) containing 1.52 g (5.0 mmol) of the 7-amino-3-(2-trifluoromethylphenyl)-2H-isoquinolin-1-one obtained in Example 38. The obtained mixture was stirred for 30 minutes. Thereafter, 2.62 g (17.5 mmol) of sodium iodide and 952.3 mg (5.0 mmol) of copper iodide (I) were added to the reaction solution, and the obtained mixture was stirred at 80° C. for 1 hour. Thereafter, the reaction solution was cooled, and a saturated sodium bicarbonate aqueous solution was added thereto, followed by extraction with ethyl acetate. The extract was washed with a saturated saline solution, and was then dried over anhydrous sodium sulfate, followed by concentration. The obtained residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:4 to 1:2), and was then washed with a sodium thiosulfate aqueous solution, so as to obtain 1.87 g (90%) of 7-iodo-3-(2-trifluoromethylphenyl)-2H-isoquinolin-1-one in the form of a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143274B2
Source datasetuspto-grants-2012_03
ORD IDord-d8ad36eec38e47068b3cfc0fc2b05e45
Source noteuspto-grants-2012_03