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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 132013Generated: October 25, 2026

Potassium Carbonate → 4-[1-(4-chloro-3-nitrophenacyl)-1H-benzimidazol-2-yl]-furazan-3-ylamine

https://huagongshe.com/reaction/132013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-(1H-benzimidazol-2-yl)-1,2,5-oxadiazol-3-amineHCID 738531—
Reactant2-Bromo-1-(4-chloro-3-nitrophenyl)ethan-1-oneHCID 2778330—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-[1-(4-chloro-3-nitrophenacyl)-1H-benzimidazol-2-yl]-furazan-3-ylamineHCID 67459004—

Reaction Steps

A suspension of 4-(1H-benzimidazol-2-yl)-furazan-3-ylamine (0.228 g, 1.14 mmol), potassium carbonate (0.40 g, 2.85 mmol) and 4-chloro-3-nitrophenacyl bromide (0.35 g, 1.25 mmol) in DMF (5 ml) is stirred at room temperature for 16 hours. The reaction mixture is diluted with ethyl acetate, washed with water and dried over sodium sulphate. Filtration of the sodium sulphate, concentration of the filtrate under reduced pressure and chromatography of the residue on silicagel using hexane-ethyl acetate as eluent gives the title compound as a solid, m.p. 198-200° C. (This compound is also listed as Example 66 in Table 1.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07385061B2
Source datasetuspto-grants-2008_06
ORD IDord-4e17a1d986e0494ebc44c1a311ec3aba
Source noteuspto-grants-2008_06