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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282927Generated: October 25, 2026

5-Nitro-2-furanmethanediol diacetate → 2-[2-(5-nitro-2-furyl)vinyl]-4-(3H)quinazolinone

https://huagongshe.com/reaction/1282927

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Nitro-2-furanmethanediol diacetateHCID 7097—
Reactant5-NitrofurfuralHCID 12774—
ReactantAnthranilamide hydrochlorideHCID 23509772—
Reactant4-({2-[2-(5-Nitrofuran-2-yl)ethenyl]quinazolin-4-yl}amino)phenolHCID 54073999—
Reactant2-Methyl-4(3H)-quinazolinoneHCID 135400457—
Product2-[2-(5-nitro-2-furyl)vinyl]-4-(3H)quinazolinoneHCID 136114329—

Reaction Steps

This example shows preparation of 2-[2-(5-nitro-2-furyl)vinyl]-4-(p-hydroxyanilino)quinazoline, (V). In this preparation, anthranilamide hydrochloride was converted to 2-methyl-4-(3H)quinazolinone (I) and 5-nitrofurfurylidene diacetate to 5-nitro-2-furancarboxaldehyde (II); (I) and (II) were then reacted to obtain 2-[2-(5-nitro-2-furyl)vinyl]-4-(3H) quinazolinone (III); (III) was then chlorinated to obtain 2-[2-(5-nitro-2-furyl)vinyl]-4-chloroquinazoline (IV) which was reacted with p-aminophenol to obtain the desired product, 2-[2-(5-nitro-2-furyl)vinyl]-4-(p-hydroxyanilino)quinazoline (V) and referred to in subsequent examples as the product of Example I. The procedure in this preparation is as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03973021
Source datasetuspto-grants-1976_08
ORD IDord-7949f31e1b6b4dab8fe54c539cf82dd9
Source noteuspto-grants-1976_08