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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710644Generated: October 27, 2026

Chlorosuccinimide → 6-Chlorooxazolo[4,5-b]pyridin-2(3H)-one

https://huagongshe.com/reaction/1710644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
ReactantOxazolo(4,5-b)pyridin-2(3H)-oneHCID 2799900—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product6-Chlorooxazolo[4,5-b]pyridin-2(3H)-oneHCID 13614459—

Reaction Conditions

Temperature85 °C

Reaction Steps

A mixture of 3H-oxazolo[4,5-b]pyridin-2-one (36) (300 mg, 2.2 mmol, 1 equiv) and NCS (352 mg, 2.65 mmol, 1.2 equiv) in 5 mL of acetonitrile was heated at 85° C. overnight. The reaction solution was diluted with ethyl acetate (EtOAc), and washed with water. The organic solution was concentrated and purified by flash chromatography, to provide 6-Chloro-3H-oxazolo[4,5-b]pyridin-2-one (37): LCMS Retention time, 0.69 min; LCMS observed (M+H)+: 171.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790726B2
Source datasetuspto-grants-2010_09
ORD IDord-b685e7efec2b47bdb2a09c8e91b76985
Source noteuspto-grants-2010_09