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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397166Generated: October 29, 2026

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

https://huagongshe.com/reaction/1397166

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 numberUS08901147B2
Source datasetuspto-grants-2014_12
ORD IDord-cd319a76c8844357a6ef9218ea54f47b
Source noteuspto-grants-2014_12