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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079673Generated: October 30, 2026

N-bromobutanimide → 5-Bromo-2-chloroquinazolin-8-ol

https://huagongshe.com/reaction/2079673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-Chloro-8-quinazolinolHCID 59199230—
SolventEthyl AcetateHCID 8857—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product5-Bromo-2-chloroquinazolin-8-olHCID 8663932260%

Reaction Conditions

Temperature0 °C

Reaction Steps

Solid NBS (1 eq) was added to a stirred solution of 2-chloroquinazolin-8-ol (1 eq) (See example 1 for synthesis) in NMP at 0° C. under argon. After stirring at 0° C. for 30 min, LCMS showed that the reaction was complete. The formation of both 5-bromo (Major) and 7-bromo (Minor) isomers along with 5,7 dibromo product was observed. The reaction mixture was diluted with ethyl acetate and washed with satd. sodium bicarbonate, water and brine. Dried, filtered and concentrated. The crude was purified by flash chromatography (3-5% EtOAc/Hexane) to provide 5-bromo-2-chloroquinazolin-8-ol as a white solid in 60% yield. ES/MS m/z 259.2 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932262B2
Source datasetuspto-grants-2011_04
ORD IDord-d6c65847e82f43298e76053d7a414829
Source noteuspto-grants-2011_04