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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846348Generated: October 31, 2026

Phenylboronic Acid → HCID 46842005, compound

https://huagongshe.com/reaction/1846348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylboronic AcidHCID 66827—
ReactantHCID 46841857HCID 46841857—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventSodium CarbonateHCID 10340—
ProductHCID 46842005HCID 4684200537.1%

Reaction Steps

Phenylboronic acid (0.067 g, 0.55 mmol) and Pd(PPh3)4 (0.005 g) were added to a mixture of 2-(5-bromopyridin-3-yl)-3-(4-chlorophenyl)quinazolin-4(3H)-one (0.190 g, 0.46 mmol) in 2 M Na2CO3 (0.5 mL) and DME (15 mL). After refluxing for 5 hours, the reaction mixture was concentrated in vacuo. The residue was dissolved in CHCl3 and washed with H2O, then brine, dried (Na2SO4), filtered, and concentrated in vacuo. Purification by flash chromatography on silica gel, eluting with 10% to 70% of EtOAc in heptane, afforded the title compound as a white solid (0.070 g, 37%). 1H-NMR (300 MHz, DMSO-d6): δ8.81 (s, 1H), 8.58 (s, 1H), 8.24 (d, J=8.1 Hz, 1H), 8.02 (s, 1H), 7.90-7.98 (m, 1H), 7.83 (d, J=7.8 Hz, 1H), 7.61-7.70 (m, 1H), 7.43-7.58 (m, 9H). MS (APCI) m/z: 410 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952021B2
Source datasetuspto-grants-2015_02
ORD IDord-ee82498460ab4b54881a52799279bb86
Source noteuspto-grants-2015_02