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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416213Generated: October 28, 2026

3-(Bromoacetyl)quinolin-2(1H)-one → HCID 10287694, compound

https://huagongshe.com/reaction/2416213

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Bromoacetyl)quinolin-2(1H)-oneHCID 22638554—
ReactantHCID 22638635HCID 22638635—
SolventMethanolHCID 887—
ProductHCID 10287694HCID 10287694—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 3-(2-bromoacetyl)-1h-quinolin-2-one (Example 27(b), 270 mg, 1.0 mmol) and 2-amino-1,1-dimethyl-1-(phenylsulfonyl)ethane-2-thione (step b, 1.7 ml, 1.0 mmol) in 3.5 ml of anhydrous MeOH was heated at 120° C. for 5 min by microwave synthesizer. The reaction mixture was cooled to RT. The precipitates were collected by filtration and washed with MeOH and CH2Cl2 to provide the title compound as a light yellow solid. Ms m/z: 411.3 (m+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06822097B1
Source datasetuspto-grants-2004_11
ORD IDord-2981c4fc07134adfbf34dd3d34f01133
Source noteuspto-grants-2004_11