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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2205113Generated: October 29, 2026

4-Cyanophenylboronic acid → HCID 86718112, compound

https://huagongshe.com/reaction/2205113

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Cyanophenylboronic acidHCID 2734326—
ReactantMethyl 3-chloro-2-phenylquinoxaline-6-carboxylateHCID 77231183—
ProductHCID 86718112HCID 8671811274.6%

Reaction Steps

The ester product was obtained via a Suzuki coupling reaction using the method previously shown in Example 13, Step 6, with methyl 3-chloro-2-phenylquinoxaline-6-carboxylate (100 mg, 0.33 mmol, 1.00 equiv) and 4-cyanophenylboronic acid (74 mg, 0.50 mmol, 1.50 equiv) as reactants. Purification via silica gel column (ethyl acetate/petroleum ether (1:20 to 1:10)) afforded 90 mg (73%) of methyl 3-(4-cyanophenyl)-2-phenylquinoxaline-6-carboxylate as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09370522B2
Source datasetuspto-grants-2016_06
ORD IDord-75784192454b42d8ad8b0631ab08539e
Source noteuspto-grants-2016_06