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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846345Generated: November 1, 2026

Phenylboronic Acid → HCID 46841854, compound

https://huagongshe.com/reaction/1846345

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylboronic AcidHCID 66827—
ReactantHCID 46841556HCID 46841556—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventSodium CarbonateHCID 10340—
ProductHCID 46841854HCID 4684185434.1%

Reaction Steps

Phenylboronic acid (0.041 g, 0.34 mmol) and Pd(PPh3)4 (0.003 g) were added to a mixture of 2-(6-bromopyridin-3-yl)-3-(4-sec-butylphenyl)quinazolin-4(3H)-one (0.150 g, 0.34 mmol) in 2 M Na2CO3 (0.3 mL) and DME (5 mL). After refluxing overnight, 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 0% to 20% of EtOAc in CH2Cl2, afforded the title compound as a white solid (0.050 g, 34%). 1H-NMR (300 MHz, DMSO-d6): δ8.63 (s, 1H), 8.22 (d, J=7.0 Hz, 1H), 7.90-8.06 (m, 3H), 7.76-7.88 (m, 3H), 7.60-7.73 (m, 1H), 7.40-7.54 (m, 3H), 7.27-7.36 (m, 2H), 7.13-7.22 (m, 2H), 2.52-2.65 (m, 1H), 1.34-1.59 (m, 2H), 1.12 (d, J=6.9 Hz, 3H), 0.56 (t, J=7.3 Hz, 3H). MS (APCI) m/z: 432 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952021B2
Source datasetuspto-grants-2015_02
ORD IDord-f0375be3828440248e9dee812899ffa0
Source noteuspto-grants-2015_02