Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850320Generated: October 26, 2026

Water → 2-(3-(3-Phenylpyrazin-2-YL)azetidin-1-YL)quinoline

https://huagongshe.com/reaction/1850320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantPhenylboronic AcidHCID 66827—
Reactant2-(3-(3-Chloropyrazin-2-yl)azetidin-1-yl)quinolineHCID 58546741—
CatalystBis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II)HCID 11714597—
Solvent1,4-DioxaneHCID 31275—
Product2-(3-(3-Phenylpyrazin-2-YL)azetidin-1-YL)quinolineHCID 5854741188%

Reaction Conditions

Temperature100 °C

Reaction Steps

A glass microwave reaction vessel was charged with 2-(3-(3-chloropyrazin-2-yl)azetidin-1-yl)quinoline (0.085 g, 0.286 mmol), phenylboronic acid (0.070 g, 0.573 mmol, Aldrich), potassium phosphate (0.152 g, 0.716 mmol, Alfa Aesar), bis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium (II) (0.020 g, 0.029 mmol, Aldrich), water (0.400 mL) and dioxane (1.6 mL). The mixture was purged with Argon gas and heated in an Initiator microwave reactor (Personal Chemistry, Biotage AB, Inc., Upssala, Sweden) at 100° C. for 30 min. LCMS showed the product. The mixture was diluted with EtOAc and washed with Na2CO3 and brine. The organic layer was dried over Na2SO4 and concentrated in vacuo. The crude was purified by silica gel chromatography (12 g, 10%-100% EtOAc-Hexane). The product was obtained as a white solid (85 mg, 88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957073B2
Source datasetuspto-grants-2015_02
ORD IDord-ff1e5fd35da5498baf2d944c354db4c7
Source noteuspto-grants-2015_02