Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsoquinoline-1-carboxylic acidHCID 68092—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantEthyl 2-(4-amino-3-bromophenyl)acetateHCID 19702145—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductEthyl (3-bromo-4-((1-isoquinolinylcarbonyl)amino)phenyl)acetateHCID 5877861869%

Reaction Conditions

Temperature60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157487B2
Source datasetuspto-grants-2007_01
ORD IDord-4f6477460f244b1295b64770b1c2e833
Source noteuspto-grants-2007_01