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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247913Generated: October 28, 2026

1H-1,2,4-Triazole → HCID 19816029, compound

https://huagongshe.com/reaction/2247913

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-1,2,4-TriazoleHCID 9257—
ReactantHCID 54360750HCID 54360750—
SolventAcetonitrileHCID 6342—
ProductHCID 19816029HCID 1981602934.1%

Reaction Steps

A mixture of 5.8 parts of 6-(chlorophenylmethyl)-2,4(1H,3H)-quinazolinedione, 10 parts of 1H-1,2,4-triazole and 158 parts of acetonitrile was stirred for 1 hour at room temperature and for 2 hours at reflux temperature. The solvent was evaporated and the residue was washed with water. The precipitate was filtered off and purified by column chromatography (silica gel; CH2Cl2 /CH3OH 90:10). The eluent of the first fraction was evaporated and the residue was washed with ethyl acetate and dried, yielding 2.2 parts (34.1%) of 6-[phenyl(1H-1,2,4-triazol-1-yl)methyl]-2,4(1H,3H)-quinazolinedione; mp. 280.9° C. (comp. 40).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05037829
Source datasetuspto-grants-1991_08
ORD IDord-9536b1be03654e8cb1c585dc57c65e95
Source noteuspto-grants-1991_08