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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374770Generated: November 1, 2026

Imidazole → HCID 136375566, compound

https://huagongshe.com/reaction/374770

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantIodineHCID 807—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 136110484HCID 136110484—
CatalystCopperHCID 23978—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 136375566HCID 136375566—

Reaction Conditions

Temperature180 °C

Reaction Steps

A stirred mixture of 2-(5-bromo-2-n-propoxyphenyl)-8-methylquinazolin-4(3H)-one (Preparation 11; 0.6 g, 0.0016 mol), anhydrous potassium carbonate (0.22 g, 0.0016 tool), copper bronze (0.1 g, 0.0016 mol), iodine (0.051 g, 0.004 mol), imidazole (0.55 g, 0.008 mol) and 1-methyl-2-pyrrolidinone (20 ml) was heated at 180° C. under a nitrogen atmosphere for 6 hours. The mixture was cooled and poured into water (150 ml), then the resulting mixture extracted with a dichloromethane-methanol mixture (9:1, 4×40 ml ). The organic extracts were combined, dried (Na2SO4) and evaporated under vacuum. The semi-solid residue was chromatographed on silica gel (10 g) using a methanol in dichloromethane elution gradient (0-4% ). Evaporation of the appropriate fractions gave the title compound which crystallized from ethyl acetate as colorless needles (0.016 g, 3%); Rf 0.5 (silica; dichloromethane-methanol 95:5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05482941
Source datasetuspto-grants-1996_01
ORD IDord-035b57eeb881459eb8dd2eafc0899bb3
Source noteuspto-grants-1996_01