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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591854Generated: October 26, 2026

p-Toluenesulfonic acid → 2-[3-(2-hydroxy-ethoxy)-5-methoxy-phenyl]-5,7-dimethoxy-3H-quinazolin-4-one

https://huagongshe.com/reaction/591854

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant2-Amino-4,6-dimethoxybenzamideHCID 20349016—
ReactantSodium BisulfiteHCID 23665763—
Reactant3-(2-Hydroxy-ethoxy)-5-methoxy-benzaldehydeHCID 86662039—
SolventDimethylacetamideHCID 31374—
Product2-[3-(2-hydroxy-ethoxy)-5-methoxy-phenyl]-5,7-dimethoxy-3H-quinazolin-4-oneHCID 136348050—

Reaction Conditions

Temperature117.5 °C

Reaction Steps

To a solution of 2-amino-4,6-dimethoxy-benzamide (7.50 g, 38.2 mmol) and 3-(2-hydroxy-ethoxy)-5-methoxy-benzaldehyde (7.50 g, 38.2 mmol) in N,N-dimethylacetamide (30 mL) was added NaHSO3 (58.5 wt %, 4.37 g, 42.0 mmol) and p-TSA (0.72 g, 3.8 mmol). The reaction mixture was heated to 115-120° C. for 16 hours, and then cooled to room temperature. N,N-dimethylacetamide was removed under reduced pressure, the residue was diluted with water (50 mL), and the solid was filtered, collected, and mixed with ether (50 mL), then filtered and dried under vacuum, to give 2-[3-(2-hydroxy-ethoxy)-5-methoxy-phenyl]-5,7-dimethoxy-3H-quinazolin-4-one as a white solid. Yield: 10 g (70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238640B2
Source datasetuspto-grants-2016_01
ORD IDord-56e74669aad44954aca2d933f3d42ff4
Source noteuspto-grants-2016_01