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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717342Generated: October 29, 2026

Acetic Anhydride → 2-(4-(Acetamidomethyl)phenyl)quinazoline-4-carboxylic acid

https://huagongshe.com/reaction/717342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant2-[4-(Aminomethyl)phenyl]quinazoline-4-carboxylic acidHCID 90411467—
SolventTetrahydrofuranHCID 8028—
Product2-(4-(Acetamidomethyl)phenyl)quinazoline-4-carboxylic acidHCID 90410708—

Reaction Conditions

Temperature25 °C

Reaction Steps

Into a 500-mL round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed 2-[4-(aminomethyl)phenyl]quinazoline-4-carboxylic acid (2.6 g, 9.31 mmol, 1.00 equiv), oxolane (200 mL) and acetyl acetate (20 mL). The resulting solution was stirred for 3 h at 25° C. The resulting mixture was concentrated under vacuum. The residue was applied onto a silica gel column with dichloromethane/methanol (20:1-5:1). This resulted in 500 mg (17%) of 2-[4-(acetamidomethyl)phenyl]quinazoline-4-carboxylic acid as a light yellow solid. MS (ESI) m/z 322 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193707B2
Source datasetuspto-grants-2015_11
ORD IDord-172515c17b7244eba00fbad47150e068
Source noteuspto-grants-2015_11