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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616106Generated: October 26, 2026

Benzyl Bromide → Methyl 2-benzyl-1-oxo-1,2-dihydroisoquinoline-7-carboxylate

https://huagongshe.com/reaction/1616106

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 1-oxo-1,2-dihydroisoquinoline-7-carboxylateHCID 60075037—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-benzyl-1-oxo-1,2-dihydroisoquinoline-7-carboxylateHCID 67282484—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of methyl 1-oxo-1,2-dihydroisoquinoline-7-carboxylate (32.5 mg, 0.16 mmol) in DMF (1.50 mL) was added potassium carbonate (66 mg, 0.48 mmol) and benzyl bromide (38.1 μL, 0.32 mmol). The reaction mixture was heated to 60° C. and stirred for 5 h. The mixture was then cooled to rt and concentrated. Water was added and the reaction mixture was extracted with DCM (5 mL, 3×). The combined organic phases were then washed with water, and brine, dried over anhydrous Na2SO4, filtered and concentrated to afford methyl 2-benzyl-1-oxo-1,2-dihydroisoquinoline-7-carboxylate. LC-MS: (FA) ES+ 294.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765773B2
Source datasetuspto-grants-2014_07
ORD IDord-0690bd31ea0844c29ae17bb213349543
Source noteuspto-grants-2014_07