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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2167232Generated: October 30, 2026

1-Naphthaldehyde → HCID 136247054, compound

https://huagongshe.com/reaction/2167232

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-NaphthaldehydeHCID 6195—
Reactant2-Amino-5-methoxybenzamideHCID 20338217—
ReactantSodium BisulfiteHCID 23665763—
SolventDimethylacetamideHCID 31374—
ProductHCID 136247054HCID 136247054—

Reaction Conditions

Temperature150 °C

Reaction Steps

Sodium hydrogen sulfite (0.8 g, 7.5 mmol) was added to a solution of 5-methoxy-2-aminobenzamide (9) (1.2 g, 7.3 mmol) and 1-naphthaldehyde (14) (1.1 g, 7.3 mmol) in N,N-dimethylacetamide (DMAC) (20 mL). The mixture was heated with stirring at 150° C. for 3 h and poured into ice water (200 mL). The precipitate was collected, washed with water, and dried in vacuo. After purification by column chromatography (silica gel; chloroform) and then recrystallization from EtOH, 6-methoxy-2-(naphthalen-1-yl)-4-quinazolinone (17) was obtained (1.5 g, 70%) as pale yellow needles. The method used to prepare 17 was used with the indicated substituted benzaldehyde and benzamide to afford 18-31. Compounds 17-31 were further analyzed by the method as described in “General materials and method”. The properties of Compounds 17-31 were respectively described as below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045437B2
Source datasetuspto-grants-2015_06
ORD IDord-76821a2ddb2b4d5aa02928381d921e4b
Source noteuspto-grants-2015_06