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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 567185Generated: October 30, 2026

Imidazole → HCID 131722283, compound

https://huagongshe.com/reaction/567185

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 18376480HCID 18376480—
ReactantHydrogen chloride-ethyl acetateHCID 21866389—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 131722283HCID 13172228349%

Reaction Conditions

Temperature92.5 °C

Reaction Steps

A mixture of 6-[4-(4-chlorophenyl)-2-(2-methyl-1-imidazolyl)-5-oxazolyl]hexyl methansulfonate(2.11 g), imidazole(660 mg), potassium carbonate(1.33 g) and N,N-dimethylformamide(40 ml) was stirred for 2 hours at 90-95° C. Water was added to the reaction mixture. The resulting mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with water, and dried(MgSO4). The residue obtained by evaporating the solvent was subjected to silica gel column chromatography. From the fraction eluted with methanol-chloroform(3:97, v/v), obtained was 4-(4-chlorophenyl)-5-[6-(i-imidazolyl)hexyl]-2-(2-methyl-1-imidazolyl)oxazole(1.26 g, 64%). The oily substance (1.26 g) was dissolved in methanol(5 ml), and thereto a 4N-hydrochloric acid-ethyl acetate solution (1.7 ml) was added. The reaction mixture was concentrated. Ethyl acetate was added to the residue. The precipitated white powder was collected by filtration. This was recrystallized from methanol-acetone to give 4-(4-chlorophenyl)-5-[6-(l-imidazolyl)hexyl]-2-(2-methyl-1-imidazolyl)oxazole dihydrochloride hemihydrate(1.16 g, 49%). mp 171-173° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06177452B1
Source datasetuspto-grants-2001_01
ORD IDord-e12e49d5856c4cddb571ece06b8c7cc1
Source noteuspto-grants-2001_01