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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1288280Generated: October 25, 2026

Aniline → 4-Amino-2-benzyl-5-phenylazopyrimid-6-one

https://huagongshe.com/reaction/1288280

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantSodium HydroxideHCID 14798—
ReactantBenzenediazonium chlorideHCID 60992—
Reactant6-amino-2-benzylpyrimidin-4(3H)-oneHCID 135596637—
SolventWaterHCID 962—
Product4-Amino-2-benzyl-5-phenylazopyrimid-6-oneHCID 136354617—

Reaction Steps

A cold solution of benzenediazonium chloride (prepared by the method well known in the art, from 2 g. aniline) was added dropwise with stirring to a solution of 4-amino-2-benzylpyrimid-6-one (4 g.) and sodium hydroxide (1.6 g.) in water (50 ml.) at 5° C. After stirring for a further 1 hour, the solid was filtered off and recrystallised from a mixture of dimethylformamide and water (4:1 v/v) to give 4-amino-2-benzyl-5-phenylazopyrimid-6-one (3.8 g.) in the form of orange needles, which decomposed at 256°-257° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03987160
Source datasetuspto-grants-1976_10
ORD IDord-1229000a61ef4024aaa189480fc98870
Source noteuspto-grants-1976_10