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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1024622Generated: October 31, 2026

CID 86596527 → (3-(2-(4-bromophenyl)-1-(4-chlorophenyl)-6-oxo-1H-purin-9(6H)-yl)phenylsulfonyl)methyl acetate

https://huagongshe.com/reaction/1024622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCID 86596527HCID 86596527—
Reactantacetic acid (3-(2-(4-bromophenyl)-1-(4-chlorophenyl)-6-oxo-1H-purin-9(6H)-yl)phenylthio)methyl acetateHCID 131731396—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product(3-(2-(4-bromophenyl)-1-(4-chlorophenyl)-6-oxo-1H-purin-9(6H)-yl)phenylsulfonyl)methyl acetateHCID 57899397—

Reaction Steps

To a stirred solution of acetic acid (3-(2-(4-bromophenyl)-1-(4-chlorophenyl)-6-oxo-1H-purin-9(6H)-yl)phenylthio)methyl acetate (3, 2.1 g, 3.6 mmol) in methanol (12 mL), dichloromethane (36 mL), magnesium monoperoxy phthalate hexahydrate (1.9 g, 3.97 mmol) is added at 0° C. The resulting solution is stirred at rt for 12 h. The reaction is quenched with the addition of saturated solution of sodium bicarbonate, and extracted with dichloromethane. The organic layer is dried over Na2SO4, concentrated. The crude product is purified by column chromatography to afford (3-(2-(4-bromophenyl)-1-(4-chlorophenyl)-6-oxo-1H-purin-9(6H)-yl)phenylsulfonyl)methyl acetate (4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722691B2
Source datasetuspto-grants-2014_05
ORD IDord-95a9db6860084cd4b9f8baa759799f62
Source noteuspto-grants-2014_05