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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 750282Generated: November 1, 2026

Triethylamine → 6-Bromo-2-(4-methanesulfonylbenzyl)-1-oxo-4-phenyl-1,2-dihydroisoquinoline-3-carboxylic acid

https://huagongshe.com/reaction/750282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Methylsulfonylbenzylamine hydrochlorideHCID 2729269—
Reactant6-Bromo-4-phenyl-3-isocoumarincarboxylic acidHCID 23060777—
SolventMethanolHCID 887—
Product6-Bromo-2-(4-methanesulfonylbenzyl)-1-oxo-4-phenyl-1,2-dihydroisoquinoline-3-carboxylic acidHCID 2306095877.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 6-bromo-4-phenyl-3-isocoumarincarboxylic acid (1.25 g) in methanol (20 ml) were added 4-methanesulfonylbenzylamine hydrochloride (1.6 g) and triethylamine (2.5 ml), and the mixture was stirred at 50° C. for 18 hrs. The solvent was evaporated under reduced pressure, and the residue was diluted with ethyl acetate, washed with 1N hydrochloric acid, and dried. The solvent was evaporated under reduced pressure. 4N Hydrochloric acid ethyl acetate solution (10 ml) was added to the residue, and the mixture was stirred at room temperature for 18 hrs. The precipitate was collected by filtration, washed with diethyl ether and dried to give the title compound (1.43 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07402595B2
Source datasetuspto-grants-2008_07
ORD IDord-87e45a618dac421f8184e542dc8a90b6
Source noteuspto-grants-2008_07