Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161853Generated: October 29, 2026

3-Chlorobenzaldehyde → HCID 59519059, compound

https://huagongshe.com/reaction/1161853

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-ChlorobenzaldehydeHCID 11477—
ReactantHCID 59519042HCID 59519042—
CatalystAcetic AcidHCID 176—
SolventEthanolHCID 702—
ProductHCID 59519059HCID 5951905960.5%

Reaction Conditions

Temperature85 °C

Reaction Steps

In a capped 20 mL scintillation vial, a solution of 2-amino-5-bromo-N-(tert-butylcarbamoylmethyl)benzamide (0.65 g, 2.0 mmol), 3-chlorobenzaldehyde (0.27 mL, 2.4 mmol) and catalytic glacial acetic acid (2 drops) in anhydrous ethanol (10 mL) was heated with stirring at 85° C. for 16 h. The resulting white suspension was cooled to room temperature, the white solid collected by suction filtration and washed with cold EtOH to give 2-[6-bromo-2-(3-chlorophenyl)-4-oxo-1,4-dihydro-2H-quinazolin-3-yl]-N-tert-butylacetamide (0.53 g, 1.21 mmol, 58%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820649B2
Source datasetuspto-grants-2010_10
ORD IDord-963c8e6b024f478f8a3151b00e7ca632
Source noteuspto-grants-2010_10