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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555521Generated: October 30, 2026

p-Toluenesulfonic acid → 2-(4-((4-ethylpiperazin-1-yl)methyl)phenyl)-5,7-dimethoxyquinazolin-4(3H)-one

https://huagongshe.com/reaction/555521

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Amino-4,6-dimethoxybenzamideHCID 20349016—
ReactantSodium BisulfiteHCID 23665763—
Reactant4-[(4-Ethylpiperazino)methyl]benzaldehydeHCID 84758526—
SolventWaterHCID 962—
SolventDimethylacetamideHCID 31374—
Product2-(4-((4-ethylpiperazin-1-yl)methyl)phenyl)-5,7-dimethoxyquinazolin-4(3H)-oneHCID 13603795828%

Reaction Conditions

Temperature150 °C

Reaction Steps

To a solution of 2-amino-4,6-dimethoxy-benzamide (150 mg, 0.76 mmol) and 4-(4-ethyl piperazin-1-ylmethyl)benzaldehyde (177 mg, 0.76 mmol) in N,N-dimethyl acetamide (10 mL), NaHSO3 (150 mg, 0.84 mmol) and p-TSA (319 mg, 1.68 mmol) were added and the reaction mixture was heated at 150° C. for 5 h. The reaction mixture was cooled to room temperature, water was added and the mixture was neutralized with NaHCO3. The solvent was removed under reduced pressure to give the crude product, which was purified by column chromatography to give 2-(4-((4-ethylpiperazin-1-yl)methyl)phenyl)-5,7-dimethoxyquinazolin-4(3H)-one (87 mg, 27%), which was converted to the hydrochloride salt. Selected data: MS (ES) m/z: 409.11; MP 278-280° C. (at decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08053440B2
Source datasetuspto-grants-2011_11
ORD IDord-933a7430243249a9b68692c848f612c4
Source noteuspto-grants-2011_11