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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846362Generated: November 1, 2026

2-amino-N-(4-chlorophenyl)benzamide → HCID 67455493, compound

https://huagongshe.com/reaction/1846362

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-amino-N-(4-chlorophenyl)benzamideHCID 670472—
Reactant3-Methyl-4-nitrobenzaldehydeHCID 11194528—
SolventEthanolHCID 702—
ProductHCID 67455493HCID 6745549348%

Reaction Steps

3-methyl-4-nitro-benzaldehyde (0.268 g, 1.60 mmol) and anyhydrous CuCl2 (0.437 g, 3.20 mmol) were added to a solution of 2-amino-N-(4-chlorophenyl)benzamide (0.400 g, 1.60 mmol) in anyhydrous EtOH (15 mL) and heated at reflux temperature for 3.5 hours. After concentration in vacuo and dissolving the residue in EtOAc, the organics were washed with H2O, then brine, dried (Na2SO4), filtered, and concentrated in vacuo. Purification by flash chromatography on silica gel, eluting with 10% to 70% EtOAc in heptane, afforded 3-(4-chlorophenyl)-2-(3-methyl-4-nitrophenyl)quinazolin-4(3H)-one (0.300 g, 48%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952021B2
Source datasetuspto-grants-2015_02
ORD IDord-dfef2c3f5ede4a928c78a1f7dcb42de2
Source noteuspto-grants-2015_02