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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13655Generated: October 25, 2026

1-(Methylsulphonyl)acetone → 6-Bromo-3-methanesulfonyl-2-methyl-4-phenyl-quinoline

https://huagongshe.com/reaction/13655

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Methylsulphonyl)acetoneHCID 78695—
Reactant2-Amino-5-bromobenzophenoneHCID 99677—
ReactantSodiumHCID 5360545—
SolventIsopropanolHCID 3776—
Product6-Bromo-3-methanesulfonyl-2-methyl-4-phenyl-quinolineHCID 1200162634%

Reaction Steps

(2-Amino-5-bromo-phenyl)-phenyl-methanone (10 g, 36 mmol), methanesulfonylacetone (7.4 g, 54 mmol) and sodium tetrachloroaureate(III) dihydrate (720 mg, 1.8 mmol) were heated at reflux in 2-propanol (100 mL) for 4.5 days. The resulting suspension was evaporated to dryness and the residue extracted with dichloromethane (2×), 1 N NaOH (2×), which removes excess of methanesulfonylacetone, and sat. NaCl (1×). The crude product was purified twice by chromatography in dichloromethane and then crystallized from dichloromethane/heptane by evaporation of dichloromethane. One obtained 4.6 g (33%) of beige crystals. MS: m/z=375/377 (M).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728142B2
Source datasetuspto-grants-2010_06
ORD IDord-e1894e98006d45e997e4443d44c97654
Source noteuspto-grants-2010_06