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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098300Generated: November 1, 2026

m-Chloroperbenzoic acid → HCID 23156868, compound

https://huagongshe.com/reaction/1098300

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 23156892HCID 23156892—
SolventDichloromethaneHCID 6344—
ProductHCID 23156868HCID 2315686879.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

20.1 mg (0.0515 mmol) of the 7-thiomorpholin-4-yl-3-(2-trifluoromethylphenyl)-2H-isoquinolin-1-one obtained in Example 104 was dissolved in 2.3 ml of methylene chloride, and 9.8 mg (0.0566 mmol) of m-chloroperbenzoic acid was further added to the solution. The obtained mixture was stirred at 0° C. for 2 hours. Thereafter, a saturated sodium bicarbonate aqueous solution was added to the reaction solution, and the obtained mixture was then extracted with methylene chloride. The extract was dried over anhydrous sodium sulfate, and was then concentrated. The obtained residue was purified by silica gel column chromatography (methylene chloride:methanol=20:1), so as to obtain 16.6 mg (79%) of 7-(1-oxothiomorpholin-4-yl)-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-12e510b113ff47dabb3aa4375b301fa8
Source noteuspto-grants-2012_03