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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247918Generated: November 2, 2026

Trimethyl orthoformate → 7-[(1H-imidazol-1-yl)phenylmethyl]-4(3H)-quinazolinone

https://huagongshe.com/reaction/2247918

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl orthoformateHCID 9005—
Reactant2-amino-4-[(1H-imidazol-1-yl)phenylmethyl]benzamideHCID 53875358—
SolventFormic AcidHCID 284—
Product7-[(1H-imidazol-1-yl)phenylmethyl]-4(3H)-quinazolinoneHCID 13598165223.6%

Reaction Steps

A mixture of 4.2 parts of 2-amino-4-[(1H-imidazol-1-yl)phenylmethyl]benzamide, 97 parts of trimethoxymethane and 1.3 parts of formic acid was stirred for 5 hours at reflux temperature and overnight at room temperature. The solvent was evaporated and the residue was dissolved in methanol. The solution was basified with ammonious methanol and then evaporated. The residue was purified twice by column chromatography (silica gel; CHCl3 /CH3OH 95:5; CHCl3 /CH3OH 90:10). The eluent of the desired fraction was evaporated and the residue was crystallized from acetonitrile. The product was filtered off, washed with 2,2'-oxybispropane and dried, yielding 1 part (23.6%) of 7-[(1H-imidazol-1-yl)phenylmethyl]-4(3H)-quinazolinone; mp. 205.0° C. (comp. 47).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05037829
Source datasetuspto-grants-1991_08
ORD IDord-c45ecfedfefa4869809a3651c02319cc
Source noteuspto-grants-1991_08