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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013781Generated: November 1, 2026

m-Chloroperbenzoic acid → HCID 59427316, compound

https://huagongshe.com/reaction/1013781

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 67318245HCID 67318245—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
ProductAmmonium HydroxideHCID 149231%
ProductHCID 59427316HCID 5942731660%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-(4-fluorophenyl)-N-(4-(7-methoxy-1,5-naphthyridin-4-ylthio)phenyl)phthalazin-1-amine (29 mg, 0.057 mmol) in CH2Cl2(2 mL) and CHCl3(3 mL) at −78° C. was added mCPBA, 77% (14 mg, 0.080 mmol) in one portion. After 1 hr, the mixture was slowly warmed to 0° C. and stirred for an additional 15 min. The solution was diluted with CH2Cl2 and washed with 10% Na2S2O4 and saturated aqueous NaHCO3. After drying the organic fraction with Na2SO4, the solvent was removed in vacuo and the residue purified by silica gel chromatography using 100% CH2Cl2 to 8% MeOH:CH2Cl2 with 1% NH4OH to afford 4-(4-fluorophenyl)-N-(4-(7-methoxy-1,5-naphthyridin-4-ylsulfinyl)phenyl)phthalazin-1-amine (18 mg, 60% yield) as a light yellow solid. MS: M+H+=522. 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981891B2
Source datasetuspto-grants-2011_07
ORD IDord-21fbaa3a35b24217948031c5b565a886
Source noteuspto-grants-2011_07