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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2359763Generated: November 2, 2026

m-Chloroperbenzoic acid → 2-Methanesulfinyl-4'-methyl-[4,5']bipyrimidinyl-2'-ylamine

https://huagongshe.com/reaction/2359763

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant4'-Methyl-2-methylsulfanyl-[4,5']bipyrimidinyl-2'-ylamineHCID 67983866—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2-Methanesulfinyl-4'-methyl-[4,5']bipyrimidinyl-2'-ylamineHCID 6798338917.2%

Reaction Steps

To a suspension of 4′-Methyl-2-methylsulfanyl-[4,5′]bipyrimidinyl-2′-ylamine (19) (380 mg, 1.629 mmol) in DCM (3.258 mL) was added mCPBA (402 mg, 1.629 mmol). The reaction turned to a brown solution, and immediately the reaction was complete. The reaction mixture was diluted with DCM and water. The organic layer was washed with saturated sodium bicarbonate and brine, dried with sodium sulfate, and concentrated. The crude residue was purified by flash chromatography with a gradient of 2-10% MeOH in DCM to give the desired product (70 mg, 17%). MS (ES+): m/z=250.1 (100) [MH+]. HPLC: tR=0.64 minute over 3 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08685993B2
Source datasetuspto-grants-2014_04
ORD IDord-f75c3bb2afe546ce9f50661154052907
Source noteuspto-grants-2014_04