HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 750135Generated: October 30, 2026
Methyl 4-(aminomethyl)benzoate → 6-bromo-2-(4-methoxycarbonylbenzyl)-1-oxo-4-phenyl-1,2-dihydroisoquinoline-3-carboxylic Acid Methyl Ester
https://huagongshe.com/reaction/750135
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl 4-(aminomethyl)benzoate | HCID 571728 | — |
| Reactant | Methyl 6-bromo-1-oxo-4-phenyl-1H-isochromene-3-carboxylate | HCID 66990710 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 6-bromo-2-(4-methoxycarbonylbenzyl)-1-oxo-4-phenyl-1,2-dihydroisoquinoline-3-carboxylic Acid Methyl Ester | HCID 44451635 | 67% |
Reaction Steps
To a solution of 6-bromo-4-phenyl-3-isocoumarincarboxylic acid methyl ester (3.60 g) in methanol (50 ml) was added 4-aminomethylbenzoic acid methyl ester (3.16 ml) and the mixture was stirred at room temperature for 18 hrs. The solvent was evaporated under reduced pressure and 1N hydrochloric acid was added, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine and dried by adding sodium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was dissolved in methanol (100 ml). Conc. sulfuric acid (10 ml) was added, and the mixture was heated under reflux for 3 hr. The solvent was evaporated under reduced pressure, water was added under ice-cooling and the mixture was neutralized with potassium carbonate. The solution was extracted with ethyl acetate and the extract was washed with saturated brine. Sodium sulfate was added to dry the mixture. The obtained residue was recrystallized from methanol to give the title compound (3.39 g, 67%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07402595B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-701a65213bfb41e49886e538a1bfebc0 |
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| Source note | uspto-grants-2008_07 |
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