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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 130330Generated: October 31, 2026

P-Anisidine → 5,7-dimethoxy-2-methyl-3-(4-methoxyphenyl)-4(3H)-quinazolinone

https://huagongshe.com/reaction/130330

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-AnisidineHCID 7732—
Reactant5,7-Dimethoxy-2-methyl-4H-benzo[d][1,3]oxazin-4-oneHCID 11506814—
SolventAcetic AcidHCID 176—
Product5,7-dimethoxy-2-methyl-3-(4-methoxyphenyl)-4(3H)-quinazolinoneHCID 1169553013.7%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a mixture of 135.5 mg (0.612 mmol) of the benzoxazinone prepared in Example 6 and glacial acetic acid (2 mL), p-anisidine (0.735 mmol) was added and the reaction mixture was heated to 60° C. for 24 hrs. The reaction mixture was concentrated in vacuo and partitioned between ethyl acetate and saturated aqueous sodium bicarbonate. The organic layer was washed with water, brine, dried over magnesium sulfate, filtered, and concentrated in vacuo to afford the product as a yellow oil (13.7% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07381730B2
Source datasetuspto-grants-2008_06
ORD IDord-68870afd840442f4b2cb00df645b91ef
Source noteuspto-grants-2008_06