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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108383Generated: November 1, 2026

HCID 67213868, compound → HCID 67213469, compound

https://huagongshe.com/reaction/2108383

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67213868HCID 67213868—
SolventMethanolHCID 887—
SolventAmmonia methanolHCID 21705897—
ProductHCID 67213469HCID 6721346985%

Reaction Steps

A stirred solution of 2-nitro-3-(4-pyridinyl)-1H-imidazole (1.19 g, 6.26 mmol) in 7N methanol/NH3 (25 ml) and methanol (25 ml) was hydrogenated at room temperature on Raney Nickel (1 g) for 4 h. The catalyst was removed by filtration and the solution evaporated. The crude product was purified by column chromatography on silica gel (dichloromethane/methanol/NH4OH 40:10:1) to yield 2-amino-3-(4-pyridinyl)-1H-imidazole (0.85 g, 85%) as a green solid. MS (ISP) 161.2 [(M+H)+]; mp 190° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514443B2
Source datasetuspto-grants-2009_04
ORD IDord-85d1371955c2468588f27f672f5f68ba
Source noteuspto-grants-2009_04