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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 583712Generated: October 26, 2026

Triethylamine → 4-[(3-Aminoisoquinolin-1-yl)ethynyl]benzoyl-2(S)-phenylsulfonylamino-beta-alanine ethyl ester

https://huagongshe.com/reaction/583712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Bromoisoquinolin-3-amineHCID 289845—
Reactant4-Ethynylbenzoyl-2(S)-phenylsulfonylamino-beta-alanine ethyl esterHCID 86752458—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product4-[(3-Aminoisoquinolin-1-yl)ethynyl]benzoyl-2(S)-phenylsulfonylamino-beta-alanine ethyl esterHCID 86754345—

Reaction Conditions

Temperature100 °C

Reaction Steps

Ethyl ester 35-3 (0.50 g, 1.25 mmol), 3-amino-1-bromoisoquinoline (0.279 g, 1.25 mmol), triethylamine (0.697 mL, 5.00 mmol), CuI (10 mg, 0.053 mmol), and (Ph3P)2PdCl2 (20 mg, 0.028 mmol) were combined in 5 mL acetonitrile in a sealed pressure tube under Ar and heated to 100° C. overnight. The dark solution was cooled and diluted with EtOAc, then washed with water (2×) and brine, dried (MgSO4), filtered, and concentrated. Flash chromatography (silica, 75% EtOAc/Hexane) gave 35-4 as a greenish foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05929120
Source datasetuspto-grants-1999_07
ORD IDord-6898179a3d1c4f5ea3eb85a2fc633743
Source noteuspto-grants-1999_07