HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372719Generated: October 26, 2026
Isoquinoline-1-carboxylic acid → Ethyl (3-bromo-4-((1-isoquinolinylcarbonyl)amino)phenyl)acetate
https://huagongshe.com/reaction/1372719
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isoquinoline-1-carboxylic acid | HCID 68092 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | Ethyl 2-(4-amino-3-bromophenyl)acetate | HCID 19702145 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl (3-bromo-4-((1-isoquinolinylcarbonyl)amino)phenyl)acetate | HCID 58778618 | 69% |
Reaction Steps
In DMF (15 ml) were dissolved 1-isoquinolinecarboxylic acid (1.00 g, 5.77 mmol), ethyl 4-amino-3-bromophenylacetate (1.49 g, 5.77 mmol), HOBt (0.39 g, 2.89 mmol), and DMAP (0.14 g, 1.15 mmol). To the resulting solution was added EDC HCl (1.33 g, 6.93 mmol). After stirring at 60° C. for 5 hours, the reaction mixture was cooled to room temperature. Water was added, followed by extraction with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate, and distilled under reduced pressure to remove the solvent. The residue was purified by chromatography on a silica gel column, whereby from n-hexane:ethyl acetate (4:1, v/v) eluate fractions, ethyl (3-bromo-4-((1-isoquinolinylcarbonyl)amino)phenyl)acetate (1.64 g, 69%) was obtained as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07157487B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-4f6477460f244b1295b64770b1c2e833 |
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| Source note | uspto-grants-2007_01 |
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