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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1431306Generated: November 1, 2026

Potassium Acetate → 5-(5,7-Difluoro-3-methyl-2-(pyridin-2-yl)quinolin-4-ylamino)-6-morpholinopyridin-3-ylboronic acid

https://huagongshe.com/reaction/1431306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium AcetateHCID 517044—
ReactantBis(pinacolato)diboraneHCID 2733548—
ReactantN-(5-bromo-2-morpholinopyridin-3-yl)-5,7-difluoro-3-methyl-2-(pyridin-2-yl)quinolin-4-amineHCID 59631101—
CatalystBis(tricyclohexylphosphine) palladium(0)HCID 2734559—
Solvent1,4-DioxaneHCID 31275—
Product5-(5,7-Difluoro-3-methyl-2-(pyridin-2-yl)quinolin-4-ylamino)-6-morpholinopyridin-3-ylboronic acidHCID 59631113—

Reaction Conditions

Temperature93 °C

Reaction Steps

A solution of N-(5-bromo-2-morpholinopyridin-3-yl)-5,7-difluoro-3-methyl-2-(pyridin-2-yl)quinolin-4-amine (395 mg, 0.77 mmol; described herein), 4,4,4′,4′,5,5,5′,5′-octamethyl-2,2′-bi(1,3,2-dioxaborolane) (215 mg, 0.85 mmol), bis(tricyclohexylphosphine)palladium(o) (25.7 mg, 0.039 mmol), potassium acetate (113 mg, 1.16 mmol), and 1,4-dioxane (10.6 mL) was stirred at 93° C. for 24 h. The reaction was then cooled to rt and partitioned between EtOAc and water. The organic layer was dried (magnesium sulfate) and concentrated, and chromatography afforded 5-(5,7-difluoro-3-methyl-2-(pyridin-2-yl)quinolin-4-ylamino)-6-morpholinopyridin-3-ylboronic acid as a yellow solid. Mass Spectrum (ESI) m/e=478.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940724B2
Source datasetuspto-grants-2015_01
ORD IDord-8cd206e51e1a44c8a2e5b31e15420eef
Source noteuspto-grants-2015_01