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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717110Generated: October 30, 2026

Potassium Acetate → 5-Methyl-1-oxo-1,2-dihydro-isoquinoline-3-boronic acid

https://huagongshe.com/reaction/717110

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium AcetateHCID 517044—
ReactantBis(pinacolato)diboraneHCID 2733548—
Reactant3-Chloro-5-methyl-2H-isoquinolin-1-oneHCID 22931033—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
Solvent1,4-DioxaneHCID 31275—
Product5-Methyl-1-oxo-1,2-dihydro-isoquinoline-3-boronic acidHCID 8981281449%

Reaction Steps

3-Chloro-5-methyl-2H-isoquinolin-1-one (100 mg, 0.52 mmol), bis(pinacolato)diboron (157 mg, 0.62 mmol), Pd(dppf)Cl2 (42 mg, 0.054 mmol) and KOAc (153 mg, 1.56 mmol) in 1,4-dioxane (2 mL) were added to a microwave vial and the reaction mixture purged with N2 for 10 min. The reaction mixture was irradiated using a microwave reactor (300 W, 120° C., 20 min). The reaction mixture was passed through a Si-thiol cartridge and concentrated in vacuo. The crude product was purified by reverse phase preparative HPLC-MS to afford 5-methyl-1-oxo-1,2-dihydro-isoquinoline-3-boronic acid as a white solid (51 mg, 49%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193689B2
Source datasetuspto-grants-2015_11
ORD IDord-b3be7816c3b24018a8ae8c5ab7e4c3e8
Source noteuspto-grants-2015_11