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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864919Generated: November 2, 2026

m-Chloroperbenzoic acid → HCID 69057118, compound

https://huagongshe.com/reaction/1864919

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantCalcium HydroxideHCID 6093208—
Reactant2-[(5R)-5-(3,5-Difluorophenyl)-2,2-dimethyl-3-oxo-4-thiomorpholinyl]-N-[(4S)-3-methyl-2,5-dioxo-1',3'-dihydrospiro[imidazolidine-4,2'-inden]-5'-yl]acetamideHCID 25020709—
SolventChloroformHCID 6212—
ProductHCID 69057118HCID 69057118—

Reaction Steps

To a solution of 2-[(5R)-5-(3,5-difluorophenyl)-2,2-dimethyl-3-oxo-4-thiomorpholinyl]-N-[(4S)-3-methyl-2,5-dioxo-1′,3′-dihydrospiro[imidazolidine-4,2′-inden]-5′-yl]acetamide (Example 2) in 1.5 mL chloroform at 0° C., was added 3-chloroperoxybenzoic acid (21 mg with a purity of 77%, 0.121 mmol). An LCMS of the reaction mixture after two hours showed that all starting material was consumed. Calcium hydroxide (14 mg, 0.185 mmol) was added to the reaction and stirred for fourty minutes. The mixture was then vacuum filtered through filter paper and the solid was washed with chloroform (3×10 mL). The filtrate was concentrated in vacuo to give a residue that was purified by silica gel chromatography, eluting with a gradient of MeOH:CH2Cl2-1:99 to 5:95, to give the title compound. MS: m/z=545 (M+H). HRMS: m/z=545.1653; calculated m/z=545.1665 for C26H26F2N4O5S.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625901B2
Source datasetuspto-grants-2009_12
ORD IDord-bcaf9ed650a04c498653dd2022454430
Source noteuspto-grants-2009_12