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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 1-oxo-1,2-dihydroisoquinoline-7-carboxylate | HCID 60075037 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 2-benzyl-1-oxo-1,2-dihydroisoquinoline-7-carboxylate | HCID 67282484 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08765773B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-0690bd31ea0844c29ae17bb213349543 |
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| Source note | uspto-grants-2014_07 |
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