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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247917Generated: November 2, 2026

1,1'-Carbonyldiimidazole → 7-[(1H-imidazol-1-yl)phenylmethyl]-2,4(1H,3H)-quinazolinedione

https://huagongshe.com/reaction/2247917

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant2-amino-4-[(1H-imidazol-1-yl)phenylmethyl]benzamideHCID 53875358—
SolventTetrahydrofuranHCID 8028—
Product7-[(1H-imidazol-1-yl)phenylmethyl]-2,4(1H,3H)-quinazolinedioneHCID 5399910335.4%

Reaction Steps

To a stirred solution of 4.6 parts of 2-amino-4-[(1H-imidazol-1-yl)phenylmethyl]benzamide in 90 parts of tetrahydrofuran were added 3.52 parts of 1,1'-carbonylbis[1H-imidazole]. The mixture was stirred first overnight at room temperature and then for 48 hours at reflux temperature. The solution was concentrated under reduced pressure and the concentrate was treated with water. The product was extracted with dichloromethane. A white product was precipitated in the dichloromethane layer. This product was filtered off and crystallized from hot acetonitrile. The product was filtered off, washed with acetonitrile and 2,2'-oxybispropane and dried in vacuo at 60°-70° C., yielding 1.77 parts (35.4%) of 7-[(1H-imidazol-1-yl)phenylmethyl]-2,4(1H,3H)-quinazolinedione; mp. 287.2° C. (comp. 29).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05037829
Source datasetuspto-grants-1991_08
ORD IDord-f9f5c0d25b354537854cabc693800556
Source noteuspto-grants-1991_08