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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029019Generated: October 31, 2026

Dichloromethane → 2-Amino-7-fluoro-3-morpholinoquinolin-6-ylboronic acid

https://huagongshe.com/reaction/1029019

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPotassium AcetateHCID 517044—
ReactantBis(pinacolato)diboraneHCID 2733548—
Reactant6-Bromo-7-fluoro-3-morpholinoquinolin-2-amineHCID 71253124—
SolventDimethylformamideHCID 6228—
Product2-Amino-7-fluoro-3-morpholinoquinolin-6-ylboronic acidHCID 71253574—

Reaction Conditions

Temperature125 °C

Reaction Steps

A microwave vessel was charged with potassium acetate (0.34 g, 3.46 mmol), [1,1′-bis(dppf)]dichloropalladium(II) complex with CH2Cl2 (0.038 g, 0.052 mmol), 4,4,4′,4′,5,5,5′,5′-octamethyl-2,2′-bi(1,3,2-dioxaborolane) (0.211 g, 0.831 mmol), 6-bromo-7-fluoro-3-morpholinoquinolin-2-amine (0.226 g, 0.693 mmol), and DMF (2.2 mL). The vessel was purged with argon, sealed, and heated by microwave radiation for 30 min at 125° C. The reaction was diluted with EtOAc (10 mL), and the suspension was filtered through celite rinsing with EtOAc. The filtrate was concentrated. The residue was purified by column chromatography on silica gel (25 mL) which had been deactivated with Et3N (2.5 mL) using 3% MeOH/DCM to afford 2-amino-7-fluoro-3-morpholinoquinolin-6-ylboronic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735384B2
Source datasetuspto-grants-2014_05
ORD IDord-4868332f76a845a280925b63c4d63bbf
Source noteuspto-grants-2014_05