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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1988784Generated: November 1, 2026

Hydrochloric Acid → HCID 178508277, compound

https://huagongshe.com/reaction/1988784

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 178474413HCID 178474413—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 178508277HCID 17850827799.6%

Reaction Conditions

Temperature86 °C

Reaction Steps

To a solution of acetylguaniidne (6.07 g, 60 mmol) in DMF (40 ml) was added a solution of 2-bromo-1-(3-bromo-phenyl)-ethanone in DMF (20 ml) dropwise at room temperature. The reaction mixture was stirred at room temperature overnight. The reaction was taken into ethyl acetate and water. After separation, the organic layer was washed with brine, dried (MgSO4) and concentrated to give the crude product. The crude product was purified via flash column (silica gel, 3% methanol in chloroform with 0.3% NH4OH) to give N-[4-(3-bromo-phenyl)-1H-imidazol-2-yl]-acetamide as a white solid (2.03 g, 36% yield). The acetamide (1.5 g, 5.38 mmol) was dissolved in a solution of 40 ml methanol and 20 ml water. The concentrated hydrochloric acid was added slowly. The reaction was heated at 86° C. for 4 hours. The reaction was concentrated to provide the HCI salt of 4-(3-bromo-phenyl)-1H-imidazol-2-ylamine (1.276 g, 86% yield). LC/MS (m/z 2378.05, 240.06 (M+H)+); HPLC Rt: 1.86 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07642273B2
Source datasetuspto-grants-2010_01
ORD IDord-74ad6df3dfce4b2e90cf1973fc3be5ac
Source noteuspto-grants-2010_01