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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1848117Generated: November 2, 2026

m-Chloroperbenzoic acid → 6-((9H-purin-9-yl)methyl)-2-(methylsulfinyl)benzo[d]oxazole

https://huagongshe.com/reaction/1848117

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant6-((9H-purin-9-yl)methyl)-2-(methylthio)benzo[d]oxazoleHCID 86681089—
SolventDichloromethaneHCID 6344—
Product6-((9H-purin-9-yl)methyl)-2-(methylsulfinyl)benzo[d]oxazoleHCID 8668109033.89%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 6-((9H-purin-9-yl)methyl)-2-(methylthio)benzo[d]oxazole (400 mg, 1.35 mmol) and m-CPBA (289 mg, 1.69 mmol) in DCM (25 mL) was stirred at 0° C. for 6 h. The reaction mixture was washed with aq Na2S2O3 and brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by silica gel chromatography eluting with 1:5 petroleum ether/ethyl acetate to give 6-((9H-purin-9-yl)methyl)-2-(methylsulfinyl)benzo[d]oxazole as a light yellow solid (143 mg, 33.89%). 1H NMR (300 MHz, CDCl3) δ 9.18 (s, 1H), 9.03 (s, 1H), 8.13 (s, 1H), 7.82 (d, J=8.4 Hz, 1H), 7.66 (s, 1H), 7.44 (d, J=9.9 Hz, 1H), 5.62 (s, 2H), 3.18 (s, 3H). LCMS (ESI) m/z 314 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952058B2
Source datasetuspto-grants-2015_02
ORD IDord-e7478cb8346c4f45ac9c4f40401598eb
Source noteuspto-grants-2015_02