Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607561Generated: November 3, 2026

Dimethyl Sulfate → 6-Bromo-3-methyl[1,3]oxazolo[4,5-b]pyridin-2(3H)-one

https://huagongshe.com/reaction/1607561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfateHCID 6497—
Reactant6-Bromo-3H-oxazolo(4,5-b)pyridin-2-oneHCID 13614458—
ReactantHCID 178418261HCID 178418261—
SolventTetrahydrofuranHCID 8028—
Product6-Bromo-3-methyl[1,3]oxazolo[4,5-b]pyridin-2(3H)-oneHCID 15926016—

Reaction Steps

To a suspension of 4.7 g of 6-bromo-oxazolo[4,5-b]pyridin-2(3H)-one (0.022 mole) in 90 ml of THF is added 24 ml of LiN(TMS)2 (0.024 mole) in THF. The homogenous solution is maintained under nitrogen at room temperature for 20 min., 3.03 g (0.024 mole) of dimethylsulfate is added and the reaction mixture allowed to stir overnight. The reaction mixture is then quenched with 20 ml of sat. ammonium chloride and extracted with 3×80 ml ethyl acetate. The ethyl acetate is then washed with 3×30 ml sat. ammonium chloride, dried over sodium sulfate and concentrated to obtain off white product which is used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04866074
Source datasetuspto-grants-1989_09
ORD IDord-5206bae8843e406692ffb49fca2e39ce
Source noteuspto-grants-1989_09